16129 Closed Entry-Level Biotechnology & Life Science Job Postings
This list includes jobs asking for Associates, Bachelors or Masters degrees and is available in three formats: chronological, alphabetical and geographical. We also keep records of all the old jobs we have posted that are no longer open: Entry-level History
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| Job Information | Description | Date Added | |
| 1 | SHL Medical Deerfield Beach, FL Process Engineer 1 B.S. in Biomedical Engineering/Mechanical Engineering or any relevant branch of study Exp: 0-2 years |
Process Engineers are responsible for supporting the implementation of new process systems into manufacturing production while ensuring that all activities are completed and documented by SHL Pharma Quality System requirements. Serving as the voice of operations between the development site and manufacturing site, the Process Engineer will be responsible for supporting the design, development, testing, and evaluation of assembly, labeling, packaging, and serialization operations. | 12/16/2025 |
| 2 | SHL Medical North Charleston, SC Operations Quality Support Bachelor’s degree Exp: 1+ years |
The Quality Support position is responsible for assisting in operation related quality documentation and tasks including but not limited to open/write up NCMRs and/or ABNs with known root cause and has standard way of revolving. This position will also be responsible for reworking activities that are approved by SHL customers but are not part of daily operation of molding and/or assembly. | 12/16/2025 |
| 3 | SK Life Science Paramus, NJ Analyst, MS&T Master’s degree Exp: 1-2 years |
Manage Contract Manufacturing Organization (CMO) in the following areas: commercial product manufacturing (Drug Substance, Drug Product & Packaging), and testing laboratories (Quality Control for stability, In-Process & Release testing). Primarily responsible for the following, but not limited to; strategy establishment and implementation of New product(s) launch, tech transfer, method/process/packaging validation, etc. Manage CPM project financial tracking. Ensure an uninterrupted supply of commercial product(s) to the marketplace. | 12/16/2025 |
| 4 | SMC Ltd Devens, MA Quality Engineer Bachelor's Degree Exp: 1-3 years |
Responsible for all areas of Quality Engineering and working directly with the engineering, tooling and manufacturing functions to ensure adequate systems and inspection methods and tools are used throughout the plants for molding or assembling products. Understanding customer requirements and implementing required documentation, action plans, purchasing equipment or tools necessary to perform tasks. Ensure proper controls, operator instructions and quality tools used to verify customer’s products meet specifications at all phases within our process. | 12/16/2025 |
| 5 | SMC Ltd Somerset, WI Operations Engineer BS in an applicable Engineering discipline Exp: 0-3 years |
Support Operations with optimal, cost-effective manufacturing processes and methods in accordance with product specification and quality standards. Manage projects from concept through successful completion that meet and exceed the customers’ requirements while matching SMC’s business needs. | 12/16/2025 |
| 6 | Smithers Darien, IL Microbiologist Master’s degree in Microbiology or related field Exp: 6 months - 3 years |
The Associate Microbiologist will conduct microbiological analysis of cannabis flower, concentrates and infused products as required by state cannabis regulatory body regulations within an ISO 17025 accredited laboratory. The Associate Microbiologist will be responsible for coordinating scheduling with the Laboratory Manager and conducting sample analysis. As time allows, the Associate Microbiologist will also be cross-trained to conduct sample onboarding, preparation, and extraction for subsequent chemical analyses. | 12/16/2025 |
| 7 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist I BA/BS Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 12/16/2025 |
| 8 | Spear Bio Woburn, MA Research Associate/Associate Scientist, Assay Development Master's degree in Biology, Biochemistry, Biophysics, Biomedical Engineering or a related discipline Exp: 1-3 years |
We are seeking a highly motivated and experienced Research Associate/Associate Scientist to join our growing Assay Development team, with hands-on experience running ultrasensitive immunoassays and the desire to be at the forefront of innovative research. This individual will play a pivotal role in advancing Spear Bio’s new range of ultrasensitive immunoassays and assay biomarker programs. | 12/16/2025 |
| 9 | Spear Bio Woburn, MA Senior Associate Scientist/Scientist, Assay Development MS in Biology, Biochemistry, Biomedical Engineering or a related discipline Exp: 1+ years |
We are seeking a highly motivated and experienced Senior Associate Scientist/Scientist to join our custom Assay Development team, who has hands-on experience developing and validating custom ultrasensitive immunoassays for clients. The ideal candidate will support the full lifecycle of assay development, from initial concept and research to validation and assay transfer. This individual will play a pivotal role in advancing Spear Bio’s new range of custom ultrasensitive immunoassays and assay biomarker programs. This role is based onsite in our lab in Woburn, MA 5 days/week. | 12/16/2025 |
| 10 | Spectrum Vascular Bridgewater, NJ Regulatory Affairs Specialist Bachelor’s degree in a scientific area Exp: 1-3 years |
The Regulatory Affairs (RA) Specialist is responsible for supporting global regulatory submissions and compliance activities to ensure medical device products meet applicable regulatory requirements throughout their lifecycle. This role collaborates cross-functionally with Quality, Engineering, Clinical, and Manufacturing teams to prepare, submit, and maintain regulatory filings with agencies such as the U.S. FDA, European Notified Bodies, and other international authorities. | 12/16/2025 |
| 11 | SRI Palo Alto, CA Mechanical Engineer Bachelors in Mechanical Engineering or a related field Exp: 1+ years |
The Bright Ceramics Technology group (BCT) is focused on developing, applying, and commercializing a unique technology platform based upon advanced materials. They develop and manufacture cutting-edge components and systems. BCT is currently searching for new grad Mechanical Engineers to join their team. The ideal candidates will be able to perform basic engineering analysis, complete detailed specifications, and be able to build and troubleshoot systems with minimal supervision. Working with interdisciplinary teams, the ME will apply their knowledge of mechanical design and materials properties to invent, fabricate, and test complex components and systems that are benchmarks of elegant and effective design. Successful applicants will be proficient in mechanical design and analysis, prototyping, a wide range of manufacturing processes, electro-mechanical systems, 3D CAD, and system fabrication. | 12/16/2025 |
| 12 | STERIS Brooklyn Park, MN Quality Analyst Bachelor’s degree in Scientific or related technical field Exp: 1 year |
The Quality Analyst in our Brooklyn Park, Minnesota location is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. In this role the Quality Analyst will lead complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. You will execute activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 12/16/2025 |
| 13 | STERIS Spartanburg, SC Quality Analyst Bachelor’s degree (Scientific or related technical field) Exp: 1 year |
The Quality Analyst in the STERIS Applied Sterilization Technologies (AST) Spartanburg, South Carolina facility is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. The Quality Analyst executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. | 12/16/2025 |
| 14 | STERIS Libertyville, IL Quality Analyst Bachelor’s degree in Scientific or related technical field Exp: 1 year |
The Quality Analyst in our Libertyville, IL location is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, and/or ISO 11137 and other applicable regulatory standards. In this role the Quality Analyst will lead complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. You will execute activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 12/16/2025 |
| 15 | STERIS Cleveland, OH Validation Engineer I Bachelor’s Degree in Mechanical Engineering, Bio Medical, Bio engineering, Chemical or Engineering General Exp: 1-5 years |
At STERIS, we’re dedicated to creating a healthier and safer world by providing innovative healthcare and life science solutions globally. We’re currently seeking a talented Validation Engineer to join our team. If you’re passionate about validation, enjoy travel, and want to be a subject matter expert, this role might be perfect for you! As a Validation Engineer at STERIS, you’ll play a crucial role in ensuring the reliability and compliance of our products in cGMP-regulated markets. You’ll author and execute validation protocols for STERIS equipment while also providing consultative support and training to our Service Representatives and Customers. Your expertise will contribute to the development and delivery of validation-related services across pharmaceutical, biotechnology, medical device, and laboratory research sectors. If you’re ready to contribute to our mission and thrive in a dynamic environment, we’d love to hear from you! | 12/16/2025 |
| 16 | Stratus Therapeutics Watertown, MA Manufacturing Associate I BA/BS degree in a science related discipline Exp: 0-2 years |
Stratus Therapeutics is seeking a motivated Manufacturing Associate/Sr. Manufacturing Associate to support routine GMP Manufacturing operations. This includes day-to-day operational tasks including but not limited to Cell Culture in a clean room environment, GMP Materials Logistics, and Environmental Monitoring within Stratus GMP manufacturing space. This is an on-site role, primarily in Watertown, MA with occasional work in Cambridge MA. Some travel between sites is required. | 12/16/2025 |
| 17 | Stryker Franklin, TN Quality Control Analyst I Master’s degree in biology, biochemistry, microbiology, or chemistry Exp: 1-2 years |
The QC Analyst I will perform routine and complex analytical testing to support lot release, stability, and method development, while accurately documenting results and ensuring all work meets cGMP/cGLP standards. | 12/16/2025 |
| 18 | Stryker Salt Laker City, UT Quality Engineer Bachelor of Science in Engineering or related discipline Exp: 0+ years |
Stryker is hiring a Quality Engineer to support our Neurovascular division in Salt Lake City, Utah. This is an onsite role requiring in-office presence 5 days per week. As Quality Engineer, you will champion quality and lean methodologies, drive process improvements, and ensure compliance to deliver superior products to patients and customers. | 12/16/2025 |
| 19 | Supernus Pharmaceuticals Rockville, MD Chemist Analytical Sciences PA Bachelor’s degree in life sciences (Chemistry degree) Exp: 0+ years |
The Chemist Analytical Sciences PA will provide analytical support for pharmaceutical solid dosage forms primarily by using dissolution testing, spectroscopy, HPLC, wet chemistry, including maintaining proper documentation. | 12/16/2025 |
| 20 | Shifamed Los Gatos, CA Manufacturing Engineer Bachelor’s in Mechanical, Biomedical Engineering or equivalent Exp: 0-3 years |
The Manufacturing Engineer contributes to medical device product design, development, manufacturing, and testing in accordance with the company’s Quality System. Helps generate design outputs where required through interface with cross-functional team members. | 12/16/2025 |
| 21 | Syner-G Worcester, MA Project Engineer Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 12/16/2025 |
| 22 | Syner-G Boston, MA Project Engineer Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 12/16/2025 |
| 23 | Synfini Menlo Park, CA Chemistry Technician Bachelor’s degree in Chemistry, Chemical Technology, or a related field Exp: 1-2 years |
We are seeking a detail-oriented and motivated Lab Operations Technician to join our chemistry laboratory team. In this role, you will support the operation of customer-facing automated synthesis workstations. You will be responsible for preparing stock solutions, maintaining the instruments, running quality control procedures and maintaining the chemical inventory. | 12/16/2025 |
| 24 | Takara Bio San Jose, CA QA Associate I BA/BS degree in a scientific discipline or engineering Exp: 0-2 years |
The QA Associate I role is responsible for providing general support to the Quality department. This role helps to maintain the quality management system under close supervision and guidance. QA Associate I is responsible for carrying out general quality functions or activities, as assigned. The QA Associate I receives guidance on workload prioritization from the team lead or management but is ultimately responsible for organizing and executing their projects and daily standard workload in a manner which meets the schedules of the operational teams whom they support. The QA Associate I is an on-site role located in San Jose, CA. | 12/16/2025 |
| 25 | Tandem Diabetes Care Barnes, CA Quality Engineer I Bachelor’s degree in Engineering, preferably Mechanical Engineering or the equivalent Exp: 6 months |
Responsible for providing quality guidance and support for product launch, sustaining engineering, production and quality system activities to assure conformance to established specifications. Facilitates the optimization and continuous improvement of internal operations to meet department, business unit and company objectives. | 12/16/2025 |
| 26 | Tandem Diabetes Care High Bluff, CA Systems Test Technician Bachelor’s degree Exp: 1 year |
Supports engineering activities such as design and execution of system level testing. Includes development of protocols, test methods, and test equipment required to verify system performance. | 12/16/2025 |
| 27 | TCG GreenChem Ewing, NJ Technician I / II (Kilo Lab) Bachelor’s degree in science or a related discipline Exp: 1-2 years |
The basic purpose is to conduct technical activities according to protocols. Receives daily tasking assignments, under moderate supervision. Functions as a member of work team by assisting others and promoting a team-oriented work environment. Performs all work in conformance with applicable regulations. Performs all work in a safe manner. Works within the laboratory or processing environment. | 12/16/2025 |
| 28 | TD2 Scottsdale, AZ Research Associate - In Vitro Pharmacology Bachelor’s degree Exp: 1-2 years |
The TD2 Research Associate - In Vitro Pharmacology is involved in many aspects of laboratory operations primarily tissue culture activities, various cell-based assays, and molecular biology experiments. This position requires great attention to detail while working in a deadline-driven environment. | 12/16/2025 |
| 29 | Tempus Research Triangle Park, NC Quality Control Reagents I - IV BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work within a cutting-edge genomics workflow to provide quality control support in a high-volume clinical molecular laboratory. Test and document new lots of reagents for clinical lab team processing and label reagents approved for use. Maintain reagent qualification records and manage quality control of reagent inventory. Document all results and findings in order to satisfy CLIA/CAP/NYS-DOH/ISO compliance. Collect and help analyze metrics. Investigate reagent related issues and help facilitate and implement corrective and preventative actions. Interact with lab management and personnel to provide training, troubleshoot issues, and prioritize QC tasks. Report significant findings/deviations and system deficiencies to lab management, as appropriate. Update SOPs and records within the document control system, including creation/ revision/ review of internal SOPs and other quality documentation. Complete Performance Qualifications (PQs) and support the Lab QC team with equipment and documentation tasks as needed. Monitor and respond to laboratory temperature excursions. | 12/16/2025 |
| 30 | Tempus Chicago, IL Molecular Technologist I/II (High Complexity) BS/MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1-2+ years |
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. | 12/16/2025 |
| 31 | Tempus Chicago, IL Molecular Technologist I (Extractions) BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 0-1+ years |
Work with a cutting-edge genomics workflow to provide high-quality data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform nucleic acid extraction and DNA/RNA quantification and qualification using robotics and automated liquid handlers. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 12/16/2025 |
| 32 | Terray Therapeutics Monrovia, CA Senior Research Associate, Protein Biophysics MSc degree Exp: 1+ years |
Terray Therapeutics is seeking a highly independent, motivated, and creative protein biochemist to join our preclinical team. An ideal candidate will have full responsibility of protein quality control workflows and be a pivotal member in collaboration between our screening and assay development teams. Successful candidates will be expected to be familiar with basic physical properties of targets of interest (based on literature and experimental sources) and play a key role in protein engineering, initial assay development and optimization. This position offers a unique opportunity to have an independent role and be a pivotal part of a multidisciplinary team in the frontiers of drug discovery. | 12/16/2025 |
| 33 | The Ritedose Corporation Columbia, SC Process Development Engineer Bachelor degree in Chemical or Mechanical Engineering Exp: 1-3 years |
Process Development Engineer is responsible for designing and implementing processes for development products. The Engineer will design and implement appropriate change requests, packing studies, batch records, forms, procedures, work instructions, risk assessments, etc. as needed to achieve the development and production goals of the organization. The Engineer’s responsibility will include Formulation, Filling, Bulk and Finished Packaging development as assigned by management. | 12/16/2025 |
| 34 | Thermo Fisher Scientific Highland Heights, KY Laboratory Supervisor, - Hematology, PBMC (2nd Shift) Bachelor's degree Exp: 1+ years |
As a Laboratory Supervisor you will play a crucial role in ensuring the smooth and efficient operation of our laboratory unit. This position involves supervising daily work activities, maintaining high standards of scientific and administrative operations, and ensuring compliance with all safety and quality protocols. Key responsibilities include operating, maintaining, and repairing clinical laboratory equipment, performing routine preventive maintenance, calibrations, and safety checks, and overseeing weekly and monthly Quality Control processes. Additionally, the supervisor will manage the Quality Control database and assist in setting up and validating new assays as directed by the manager. | 12/16/2025 |
| 35 | Thermo Fisher Scientific Worcester, MA Associate Scientist – Buffer / Media Preparation Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Exp: 0-2 years |
Independently performs routine and non-routine testing. Performs laboratory scale activities to support PDS&T, Pilot Lab Process Development. These activities range from media/buffer preparation to direct project support under the supervision of relevant subject matter experts. Successfully manages time to execute activities within project demands. Manages consumable and raw material forecasting and stocking in a high-volume laboratory setting. Recognizes and resolves moderate challenges in the lab space with their routine workflows. Actively enhances and recommends new workflows based on the evolving needs of the Pilot Lab and PDS&T teams. | 12/16/2025 |
| 36 | Thermo Fisher Scientific Greenville, NC QC Scientist I (12 hour Night Shift) Bachelor’s degree in a biology/ related field Exp: 1+ years |
A successful person will perform Environmental Monitoring tasks in support of Steriles production within classified areas. The individual is encouraged to follow the 4i Values that are held in high regards by the company when completing their work. The four values are integrity, innovation, intensity, and involvement. The job function includes aseptic technique which requires the individual to gain knowledge of aseptic gowning as well as working in cleanrooms in order to monitor the area while sterile products are filled and manufactured. Typical shift hours are 6pm-6am on a 2-2-3 rotating schedule. | 12/16/2025 |
| 37 | Thermo Fisher Scientific Cincinnati, OH Scientist II, Manufacturing Sciences Bachelor's degree in chemical engineering (or other engineering field), chemistry, pharmacy, or other related science or technical field Exp: 1-3 years |
As a Manufacturing Scientist II, you will lead and/or implement activities for the development of new and established manufacturing processes of solids, liquids, and semi-solid dosage forms. Project management skills will be applied to implement the scaling up manufacturing processes, supporting new product validations and post approval qualifications activities. This will require the writing, approval, and routing documents within a manufacturing setting. You will be the primary technical representative on client projects and will work closely work with internal and external project teams of analytical, quality, and project management representatives. Supporting process development and commercial activities will be required. Leads technical/scientific project activities and discussions to lead strategies and technical solutions that meet client needs and expectations. | 12/16/2025 |
| 38 | Thermo Fisher Scientific Middleton, WI EHS Manager Bachelor's or Master's degree in occupational safety, environmental health, life science or natural science or equivalent Exp: 1+ years |
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. | 12/16/2025 |
| 39 | Thermo Fisher Scientific Middleton, WI Lab Supervisor (GMP, Biopharmaceuticals) Bachelor's degree Exp: 1+ years |
As a Lab Supervisor you will coordinate staffing and resources, support day-to-day workflows, and assist in preparation and implementation of company policies, quality systems and training programs. This role ensures that projects are completed in a timely manner so that company revenues are met, and clients are satisfied with the quality and turnaround of work being performed. The Lab Supervisor also ensures that staff continue to be developed to keep pace with department goals and growth. | 12/16/2025 |
| 40 | Thermo Fisher Scientific Cincinnati, OH Equipment Engineer II Bachelor’s Degree in Engineering (industrial, manufacturing, chemical, or mechanical engineering) Exp: 1+ years |
Carries out management of engineering projects including estimating costs, sourcing, identifying, specifying, purchasing and installing equipment, crafting/modifying existing or new facilities, and the commissioning and qualification of equipment, utilities and facilities to meet site/company requirements. | 12/16/2025 |
| 41 | Pfizer Sanford, NC Engineering Validation Associate Bachelor's degree Exp: 0+ years |
Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with regulatory requirements and company policies. Troubleshoot validation problems for equipment and performance processes, conducting statistical analysis of testing results to address process anomalies. Write, review, and approve validation process documents and technical reports related to equipment, products, and processes. Contribute to project tasks and milestones, organizing work to meet deadlines and applying basic team effectiveness skills within the immediate Work Team. Make decisions within limited options to resolve basic problems, working under the supervisor's direction and seeking guidance from colleagues. Ensure work is regularly reviewed for technical judgment, completeness, and accuracy, exercising judgment with reliance on the supervisor. Determine the process capability of new equipment through the execution of approved protocols, incorporating defined parameters into operating procedures and batch records. Assist with the development of validation protocols, manage regulatory queries and responses, and participate in deviation investigations to identify root causes and define corrective and preventative actions. Adhere to all company and Good Manufacturing Practices (cGMP) procedures, safety regulations, and participate in the development of validation programs to stay current with cGMPs and industry standards. Work effectively as a member of the Engineering Validation team, collaborating with Business Area Training Leads, Coordinators, and SMEs to support cGMP and site training initiatives, reporting to the Validation Section Manager and summarizing data into concise reports for review and approval. | 12/08/2025 |
| 42 | Pfizer Rocky Mount, NC Tech Services - Senior Associate Engineer Master's degree Exp: 0+ years |
As a Senior Tech Ops Engineer, you will play a crucial role in improving patients' lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients' lives. The Sr Tech Ops Engineer provides strategic direction and technical expertise for site Commissioning and Qualification (C&Q) activities for equipment, utilities and facilities. To include execution of C&Q work for utilities, facilities and global applications as well as maintenance and execution of periodic performance qualification schedule and reviews. This role serves as a Center of Excellence, driving alignment with global and industry engineering standards. The engineer supports site critical programs related to C&Q while also supporting capital project execution and site-wide technical initiatives. The position plays a key role in shaping the site’s technology roadmap, ensuring operational excellence, and fostering a self-sustaining technical work structure for the Focus Factory Manufacturing Technology teams. | 12/08/2025 |
| 43 | Pfizer Rocky Mount, NC Sr. Associate, Learning & Development (L&D II) Master's degree Exp: 0+ years |
In this role, you will act as a change agent, facilitate job shadowing and apprenticeship programs, manage knowledge management, and conduct operator trainer qualifications. You will design and update curricula plans, manage strategic change initiatives, assist in developing departmental strategy by designing training and L&D programs, and participate in continuous improvement projects. You will provide metrics and insights related to training, learning and development. You will collaborate with area SMEs to ensure that our programs support colleague growth, improve human performance, and enable comfort and proficiency with digital systems/tools. This position will report to the Manager, Learning and Development within the Strategy & Operational Excellence organization and be dedicated to supporting a Focus Factory. It is your dedication and hard work that will make it possible for Pfizer’s customers and patients to receive the medicines they need, when they need them. | 12/08/2025 |
| 44 | Pfizer Pearl River, NY Associate Scientist, Immunology Bachelor’s degree in a relevant scientific discipline (e.g., Biology, Immunology, Biochemistry) Exp: 0-2 years |
As an Associate Scientist in the CMI group, you will play a critical role in generating high-quality cellular immunology data in a regulated laboratory setting to support Pfizer’s vaccine programs. The primary focus of this role is high-throughput flow cytometry to analyze cellular immune responses in clinical and non-clinical samples. You may also support additional immunological assays such as ELISPOT and other biofunctional methods. This position involves routine testing, assay development, and data analysis, all performed in compliance with Good Laboratory Practices (GLP) and internal standards. | 12/08/2025 |
| 45 | Pfizer Rocky Mount, NC Senior Automation Engineer Master's degree Exp: 0+ years |
As a Sr. Automation Engineer your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate explaining difficult issues and establishing consensus between teams. It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe. | 12/08/2025 |
| 46 | Pfizer Sanford, NC EM Analyst I Bachelor’s degree Exp: 0 years |
Conduct and support laboratory operations, including sample preparation, data collection, and analysis. Apply technical skills to assignments, ensuring high-quality results and solving moderately complex problems with sound judgment. Follow procedures with general instructions, maintaining compliance with regulatory standards and working under moderate supervision. Identify activities to support team goals, contributing to overall project success and ensuring adherence to project timelines. Perform testing on clinical and commercial products, raw materials, and validation samples, maintaining a neat and orderly work area. Independently write Standard Operating Procedures, technical reports, project plans, and other documents. Train junior colleagues, develop training plans, oversee training activities, and handle laboratory investigations for events and Out of Stock results. Create, review, and approve compliant test method transfer and validation protocols, reports, and equipment qualification/computer validation records. | 12/08/2025 |
| 47 | Pillar Biosciences Natick, MA Supply Chain Generalist Bachelor’s degree Exp: 0-2 years |
This entry level position plays a critical role supporting supply chain within a fast paced environment. The range of duties include but are not limited to: generating purchase orders for re-order point and MRO items, daily cycle counts, supplier/customer on time order tracking, assisting with international customs documents and picklist as needed. This newly created position requires strong attention to detail and the ability to track data to help drive metric improvements. | 12/08/2025 |
| 48 | Pledge Therapeutics Canton, MA Research Associate, Immuno-Oncology MS Exp: 1-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our new state-of-the-art facility in Canton, MA. The successful candidate will engage in the Immuno Oncology research areas of the company and will work with a successful team of international senior scientists located in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 12/08/2025 |
| 49 | Pledge Therapeutics Canton, MA Research Associate, Virology Bachelor’s or Master’s degree in biological sciences or a related field Exp: 0-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our state-of-the-art facility in Canton, MA. The successful candidate will engage in the company’s virology research areas and work with a successful team of scientists in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 12/08/2025 |
| 50 | PROCEPT BioRobotics San Jose, CA Quality Engineer, Sustaining Bachelor’s degree in Engineering (Mechanical, Biomedical, Industrial, or related field), Life Sciences, or equivalent Exp: 1-3 years |
Do you want to be part of an innovative, cutting edge technology, robotics company that is changing how BPH is treated? Are you looking to be part of an enthusiastic, driven, passionate and challenging team, who continuously learn from one another? Are you a leader who wants to make a difference and improve processes? Are you detailed-oriented? At PROCEPT BioRobotics you will have an opportunity to contribute and greatly support our continuous improvement philosophy by being part of our Quality Engineering team. This position has a unique impact on the quality and reliability of our devices. You will work with cross-functional teams to maintain and improve the Quality System within the requirements of FDA's Quality System Regulation (QSR), ISO 13485 (ISO) and EU MDR. Being detail and solution oriented, proactive, and self-managed will assist in the success of this position. | 12/08/2025 |
| 51 | PROCEPT BioRobotics San Jose, CA Reliability Quality Engineer Master’s degree in Mechanical, Biomedical, or Electrical/Electronic Engineering Exp: 1 year |
As PROCEPT BioRobotics continues to expand, the Design Quality Assurance group is seeking a Reliability Quality Engineer to support ongoing reliability initiatives. The Reliability Quality Engineer will collaborate with product development and sustaining teams to ensure that PROCEPT BioRobotics delivers highly reliable products through the application of reliability tools such as Weibull Analysis, Failure Mode Effects & Criticality Analysis (FMECA), Fault Tree Analysis (FTA), structured problem-solving, reliability modeling, reliability predictions, and reliability testing. | 12/08/2025 |
| 52 | Pro-Dex Irvine, CA Manufacturing Engineer Bachelor’s Degree of Science in Mechanical Engineering or related field Exp: 1-2 years |
Works with and across the various disciplines of the engineering team, machine shop personnel, and assembly floor personnel for project realization, manufacturability, inspection, and assembly of product. One of the primary functions of the position is to create, develop, and establish cost effective processes and procedures for manufacturability, inspection, and assembly to reduce cost and improve fabrication methods that meet the product specifications and requirements across various projects. | 12/08/2025 |
| 53 | Profluent Emeryville, CA Research Associate I/II, Platform Discovery BS or MS in molecular biology, biochemistry, or a related field Exp: 0-5 years |
We are seeking a motivated and creative Research Associate I/II to join our Platform Discovery team. You will work closely with more senior team members to evaluate and optimize methods for the delivery of our novel gene editing systems in therapeutically relevant cell types. This includes developing robust high-throughput workflows in biochemical and/or cell-based systems. Your work will be critical for enabling new therapeutic opportunities. The ideal candidate will have extensive experience with molecular cloning, mammalian cell culture techniques, and assay development. This is an excellent opportunity to work cross-functionally with a diverse team of experts across AI and machine learning, protein design, cell biology, and gene editing. | 12/08/2025 |
| 54 | Prolific Machines Emeryville, CA Research Associate II/III, Biology (Contract) Master's degree Exp: 1+ years |
We are looking for a highly motivated and detail-oriented RA II or Sr. RA to drive mammalian cell culture-based protein production workflows at Prolific. We are a team of scientists using light to control the expression of biotherapeutic proteins, increasing titer and improving quality attributes. We are rapidly expanding our capabilities in mammalian cell line engineering, stable cell line generation, and driving production runs to produce therapeutic proteins. You will be instrumental in optimizing and executing cell line development and protein production which will support multiple projects. Your responsibilities will include maintenance and engineering of mammalian suspension cell lines (including CHO), handling, seeding, and sampling runs for protein production, and contributing to downstream readouts such as Octet BLI, flow cytometry, and metabolite measurements (such as Nova). Your knowledge of mammalian cell line development techniques, combined with your attention to detail and motivation to learn will make you highly effective in this role. The ideal candidate for this role is energized by hands-on technical work and takes pride in owning and refining routine cell line generation processes for high quality results. You’ll get to work cross collaboratively with team members in optogenetics, synthetic biology, cell line development, hardware engineering, bioprocessing, and data science disciplines to establish cell lines crucial to Prolific’s success. This is a unique position and opportunity to drive cell culture workflows in an exciting startup setting. You’ll be provided with room for technical growth and receive mentorship to help you succeed. This role is based on-site in our headquarters in Emeryville, CA. The contract is expected to last for 6+ months with the possibility of extension or conversion to full-time employee at the end of the term. | 12/08/2025 |
| 55 | Prolific Machines Emeryville, CA Research Associate II/III, Molecular Biology (Contract) Master's degree Exp: 1+ years |
We are looking for a highly motivated and detail-oriented RA II or Sr. RA to drive molecular biology-based workflows at Prolific. We are a team of scientists using light to control expression of biotherapeutic proteins, increasing titer and improving quality attributes. You will be instrumental in spearheading the top-of-funnel vector development processes which form the foundation for our cell line development pipeline. Your responsibilities will focus around the design and assembly of DNA vectors for downstream cell line engineering applications. Your knowledge of molecular biology techniques, combined with your attention to detail and motivation to learn, will make you highly effective in this role. The ideal candidate for this role is energized by hands-on technical work and takes pride in owning and refining routine molecular biology processes for high quality results. You’ll get to work cross collaboratively with team members in optogenetics, synthetic biology, cell line development, hardware engineering, bioprocessing, and data science disciplines to establish cell lines crucial to Prolific’s success. This is a unique position and opportunity to drive foundational workflows in an exciting startup setting. You’ll be provided with room for technical growth and receive mentorship to help you succeed. This role is based on-site in our headquarters in Emeryville, CA. The contract is expected to last for 6+ months with the possibility of extension or conversion to full-time employee at the end of the term. | 12/08/2025 |
| 56 | Prolific Machines Emeryville, CA Electrical Engineer MSE Exp: 1+ years |
We’re looking for an Electrical Engineer to support design, testing, and integration of electronic systems that power our advanced biomanufacturing platforms. You’ll collaborate closely with hardware, software, and bioengineering teams to ensure our electrical subsystems meet performance, safety, and reliability requirements. This role will be based on-site in Emeryville, CA and will report to the Senior Mechatronics Engineer of the company. Standard hours will be 40hrs per week, with the employee aiming to be onsite during the company’s core hours Monday-Friday, 10am-4pm. | 12/08/2025 |
| 57 | PsychoGenics Paramus, NJ Research Associate 2 Bachelor’s degree in biological sciences neuroscience, or related field Exp: 1-3 years |
We are looking for a highly motivated Researcher to join our neuropharmacology group. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The primary responsibilities of the candidate will include, but are not limited to, dosing animals, surgical nursing, conducting behavioral assessments, and dissection and tissue collection. The candidate will be responsible for coordinating studies and the proper execution of experiments. The candidate must be capable of working both across teams and independently. | 12/08/2025 |
| 58 | Quality Agents Rockville, MD Validation Engineer I BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. | 12/08/2025 |
| 59 | Quality Agents Rockville, MD Quality Assurance Specialist BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Quality Assurance Specialists are leading service providers to our clients providing GMP support. The individual will coordinate validation activities with the client and meet timelines. | 12/08/2025 |
| 60 | Quva Sugar Land, TX Production Technician I - Formulation Bachelor’s degree with an emphasis in Chemistry, Biochemistry or equivalent Exp: 1 year |
Our Production Technician I – Formulation plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical product. Once you complete our training, your responsibilities will include supporting daily manufacturing activities for non-sterile and sterile bulk/CSP operations. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. | 12/08/2025 |
| 61 | Quva Bloomsbury, NJ QC Laboratory Technician Bachelor’s Degree in life science or related field Exp: 1-2 years |
Our QC Laboratory Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing basic laboratory support functions related to the management of laboratory samples, materials, and testing supplies. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. | 12/08/2025 |
| 62 | Reckitt Salt Lake City, UT R&D PDM Assistant BS/BA degree in a related science Exp: 0-2 years |
The R&D Operations Assistant will work with technical product development on key projects for the R&D team. | 12/08/2025 |
| 63 | Reckitt Belle Mead, TN Quality Compliance Assistant B.S. degree in a science field required, preferably Chemistry Exp: 0-2 years |
In R&D, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centers of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organization means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our R&D Academy, designed to develop our team and allow you to grow in our great organization. | 12/08/2025 |
| 64 | Regeneron Tarrytown, NY Process Development Associate, Bioreactor & Scale-Up Development BS or MS in Chemical Engineering or Bio-related Engineering Exp: 0-2 years |
Regeneron’s Bioreactor and Scale-Up Development Group within Preclinical Manufacturing and Process Development (PMPD) is looking for a motivated Process Development Associate to work as part of the late-stage development team to develop production processes of biologics in a non-GMP process development laboratory. In this role, they will perform studies at pilot scale to develop commercially enabling manufacturing processes. | 12/08/2025 |
| 65 | Regeneron Tarrytown, NY Senior Associate Scientist Bachelors degree Exp: 1-4 years |
We are looking for an R&D Associate to join the DNA Core facility. We provide Regeneron laboratories with services vital for conducting scientific research. These services include plasmid preparation and purification. | 12/08/2025 |
| 66 | Regeneron Tarrytown, NY Process Development Associate (PMPD) - Late Stage Cell Culture BS or MS in Chemical Engineering or Bio-related Engineering Exp: 0-2 years |
Regeneron’s Cell Culture Development Group within Preclinical Manufacturing and Process Development (PMPD) is looking for a motivated Process Development Associate to work as part of the late stage development team to develop production processes of monoclonal antibodies in a non-GMP process development laboratory. In this role, they will perform studies at bench scale in support of clinical or commercial manufacturing production. | 12/08/2025 |
| 67 | Regeneron Tarrytown, NY Process Development Engineer I, Analytics (PMPD) MS degree Exp: 0-3 years |
Regeneron's Preclinical Manufacturing & Process Development (PMPD) Analytics group is seeking a Process Development Engineer I interested in the analytical characterization of biopharmaceuticals. In this exciting role, you will conduct analytical experiments that support manufacturing process development and research activities in a fast-paced, high-throughput laboratory setting. | 12/08/2025 |
| 68 | Regeneron Tarrytown, NY Process Development Engineer I - Late Stage Purification (PMPD) Master’s degree in either Chemical Engineering, Biochemical Engineering, Biochemistry, or a related field Exp: 0-3 years |
Regeneron’s Late-Stage Purification Development team within PMPD (Preclinical Manufacturing and Process Development) is seeking a full-time Process Development Engineer I. In this role, you will be responsible for the development and transfer of the harvest, affinity chromatography, and viral inactivation unit operations for recombinant proteins using Quality by Design principles. | 12/08/2025 |
| 69 | Regeneron Tarrytown, NY Process Development Associate - Pilot Scale Purification Development (PMPD) Bachelor’s and/or Master’s degree in either Chemical Engineering, Biochemical Engineering, or Biochemistry Exp: 1-5+ years |
Regeneron's Preclinical Manufacturing & Process Development Group (PMPD) is seeking a Process Development Associate as a full time position to work in the Purification Development group. In this role, you will be responsible for the purification at pilot scale of a variety of clinical biologics, building systems to support the planning and execution of pilot scale work, and investigating technologies to support the scalability of pilot scale operations. The ideal candidate will be hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment. This is a lab based role focused on pilot scale operations, requiring a significant amount of physical activity. | 12/08/2025 |
| 70 | Regeneron Tarrytown, NY Associate Scientist, Non Viral Delivery Technologies BS/MS in chemistry, molecular biology, biochemistry, bioengineering, or related field Exp: 0-2+ years |
We are seeking a highly motivated Associate Scientist to join the Non-Viral Delivery Technologies group within Regeneron Genetics Medicines. Our team works closely with all the other teams in the Genetics Medicines group to produce and develop lipid nanoparticles (LNPs) to support their programs. You will work on the LNP production core as well as conduct ligand targeted LNP development work. | 12/08/2025 |
| 71 | REGENXBIO Rockville, MD Associate Scientist, Bioanalytical Lab & QC Support Master’s degree in a relevant scientific field Exp: 1+ years |
As a member of our Bioanalytical Sciences team, you will be responsible for performing nonclinical and clinical sample testing (PK, Immunogenicity, PCR, etc.) following developed, qualified, and/or validated bioanalytical methods in support of REGENXBIO projects and programs. You will also be responsible for developing and validating bioanalytical methods for gene therapy products. You will also be responsible for performing QC review of documentation produced in the Bioanalytical laboratory, including assay runs, summary tables, reports, protocols and collaborate with various departments to ensure compliance with regulatory expectations. | 12/08/2025 |
| 72 | Revolution Medicines Redwood City, CA Safety Scientist MSc in a Life sciences discipline Exp: 1+ years |
The Safety Scientist within Global Patient Safety Science is an individual contributor who provides safety science and pharmacovigilance support to all products across the RevMed portfolio, which includes early and late phase development activities. The individual will be responsible for supporting clinical studies, review of clinical trial protocols, supporting updates to IBs, ICFs, and authoring of DSURs. Additional safety related activities will involve medical review of individual case safety reports (ICSRs), safety surveillance of assigned products and active member of cross-functional teams. | 12/08/2025 |
| 73 | Revvity San Diego, CA Biochemist I - Recombinant Protein Manufacturing Bachelor of Science in in Life Science or related area Exp: 6 months |
BioLegend is seeking a Biochemist I join our recombinant protein manufacturing team. The Biochemist I is responsible for producing recombinant protein products using bacterial cell culture systems. This role involves multiple stages of production, including protein expression, purification, and quality support. Key responsibilities include preparing buffer solutions, culture media, and dilution reagents; performing bacterial cell cultures; purifying recombinant proteins via affinity methods; and conducting DNA isolations following standard operating procedures. | 12/08/2025 |
| 74 | Revvity San Diego, CA Quality Control Associate I, Flow Cytometry (PM Shift) Bachelor’s degree in a scientific discipline Exp: 6+ months |
At BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team. | 12/08/2025 |
| 75 | Rion Rochester, MN Research Associate, Analytical Development Bachelor’s or Master’s degree with focus in Biological Sciences Exp: 1+ years |
The Analytical Development Research Associate will contribute to analytical method development, implementation, and pre-qualification of methods focused on Rion’s exosome technology. This role will work closely with Rion Quality Control to execute method transfers and support continuous improvement. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, ELISA, RT-qPCR, HPLC and colorimetric/fluorometric-based assays. The Analytical Development Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Analytical Development Research Associate will work closely with the Analytical Development Scientists and support the efforts of Quality Control/Process Development. As such, the successful candidate will work in an upbeat, highly collaborative and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 12/08/2025 |
| 76 | Sanguine Biosciences Los Angeles, CA Apheresis Operations Specialist I Bachelor's Degree in a life science or other related field Exp: 1-2 years |
The role of the Apheresis Operations Specialist I is to serve as a primary point of contact for both our donors participating in apheresis collections and our partner site contacts. The AOS I is responsible for screening and qualifying donors who are part of an extensive Sanguine database, and those who are identified by the Patient Recruitment and Marketing Team. The AOS I will screen potential donors to obtain the necessary health information, conduct medical record reviews to qualify donors for apheresis research studies, and provide a seamless experience for our donors. The Apheresis Operations Specialist is also responsible for collecting all necessary documents, coordinating with apheresis sites to schedule donors and pick up services, maintaining patient data and documenting results, fielding real-time calls and emails, and striving to provide a seamless experience for our donors. This individual will be a part of our Apheresis Operations team and will work cross-functionally with multiple departments including Project Management, Patient Operations, and apheresis site points-of-contact. | 12/08/2025 |
| 77 | Sanguine Biosciences San Diego, CA Laboratory Technician I Bachelor’s degree Exp: 1 year |
The Entry Level Lab Technician I will be responsible for the processing and testing of various blood samples. Sample processing will include, but is not limited to: PBMC, T, B, & NK cell isolations. Other assigned duties may include cell counting, aliquot preparation, accessioning, reagent creation, proper storage, flow cytometry lab services. Initial samples will be from both Leukopaks and blood samples or its derivatives. This role will also require experience with LIMS systems and commercial laboratory operations, including the internal communication of project details with Sanguine personnel as well as the ability to work as a team. | 12/08/2025 |
| 78 | Science 37 Morrisville, NC Supply Associate Bachelor’s degree Exp: 1 year |
The Supply Associate position is responsible for assisting with the management of clinical supplies and equipment used in clinical studies. The Supply Associate is responsible for preparing and shipping study supplies to study participants and study staff, maintenance and accountability of study supplies and nursing equipment, ordering of supplies, and inventory management. The Supply Associate works closely with the Supply team, PI, sub-Is and study team to ensure safe and efficient conduct of clinical studies. | 12/08/2025 |
| 79 | Serán Bend, OR Scientist/Engineer, Drug Product Development Bachelor or Master’s degree in pharmaceutical science, chemistry, chemical engineering, biological engineering, mechanical engineering, materials scie Exp: 1 year |
Serán seeks to hire a Scientist/Engineer to join the Drug Product Development group and contribute as part of an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. The role requires strong hands-on laboratory skills and the ability to apply fundamental scientific principles to solve problems. Strengths in data collection, analysis, proactive communication, and continuous learning by textbooks, journals, and training will enable the successful candidate to thrive. The ideal candidate would enjoy a work environment that is both science-focused and adaptable to meet | 12/08/2025 |
| 80 | Serán Bend, OR Associate I, Sample Management Coordinator Bachelor’s degree in a scientific discipline Exp: 1 year |
Serán BioScience is searching for an organized and detail oriented Associate to support the Sample Management Program within the Quality Control Department. The QC Associate I, Sample Management Coordinator plays a key role supporting sample coordination by managing sample inventory, including the receipt, handling, shipment, and storage of samples supporting the GMP retention program, stability program, and external Contract Testing Laboratories (CTL) testing. All necessary training provided. Those with an interest in starting a career in bioscience are encouraged to apply. | 12/08/2025 |
| 81 | NorthStar Beloit, WI Radiopharmaceutical Manufacturing Associate Bachelor's Degree in a STEM discipline Exp: 1 year |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. | 12/01/2025 |
| 82 | Nuclein Austin, TX Technical Applications Specialist I Bachelor’s degree in a relevant field (Biology, Molecular Biology, or similar discipline) Exp: 1-2 years |
Position objective is to provide a high degree of direct support to end-user customers with the primary goal of ensuring on-going customer satisfaction. Accomplished by providing a high level of rapid and complete customer service through answering inquiries, problem resolution, customer communication and ensuring correct internal response to customer identified potential or actual issues which could impact the safety and efficacy of Nuclein provided products. | 12/01/2025 |
| 83 | Oakwood Labs Solon, OH Quality Control Chemist Bachelor's degree in Chemistry, Biochemistry, Biology, or related field Exp: 1-2 years |
Perform analytical testing of raw material, in-process product, final product release and stability testing. Clear documentation of test activities in approved worksheets and laboratory notebooks. Execute mathematical calculations as outlined in test methods. Assess data to determine if the material tested meets specifications. Peer review of quality control data. Participate in investigational testing and assist with root cause analysis. Create and review SOP’s and author Change Controls. Other general lab related duties as necessary. | 12/01/2025 |
| 84 | Obsidian Therapeutics Bedford, MA Research Associate, Process Development BS or MS degree in chemical engineering, biochemical engineering, biology or relevant field Exp: 0-2 years |
We’re looking for a highly motivated, flexible, and collaborative Research Associate with experience in, and a passion for—cell culture and process development. Based at our Bedford, MA location, you’ll contribute to developing and characterizing manufacturing processes for cell therapy products targeting cancer. You’ll be a vital part of a highly collaborative Technical Operations team, working to achieve Obsidian’s vision by translating innovative science into medical breakthroughs for patients, starting with our lead program, OBX-115—a novel engineered tumor-infiltrating lymphocyte (TIL) therapy. | 12/01/2025 |
| 85 | Olympus San Jose, CA Repair Engineer I Bachelor's degree in engineering Exp: 1 year |
Provide engineering support for introduction of new products and alternate repair activities. Function as Project Coordinator on more complicated projects as defined by the Manager by providing technical information to other project participants recommending cost effective procedures tracking and maintaining implementation dates and documenting completed projects. Provide support to Associate Engineer on his/her assigned projects. | 12/01/2025 |
| 86 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology B.S. degree in Biological or related sciences Exp: 1 year |
The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned supervisor, commercial manufacturing, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 12/01/2025 |
| 87 | Orchid Orthopedic Solutions Bridgeport, MI Quality Engineer, Sustaining Product Quality Bachelor of Science (B.S) Exp: No exp |
The Quality Engineer I supports the ongoing quality of Orchid's legacy products & processes and works cross-functionally to sustain the business. | 12/01/2025 |
| 88 | OrganaBio Irvine, CA On-Call Cell Processing Associate Bachelor Degree in Biology, Cell and Molecular Biology, Biotechnology, Biomedical Engineering, or related field Exp: 1-2 years |
A Cell Processing Associate assists in the performance of primary peripheral blood mononuclear cells (PBMCs) isolation from patient samples, as part of screening efforts for various customers. This position will help contribute to PBMC isolation process improvement, to drive efficiency in the documentation and production process. This role will support Process Development (PD) team efforts, and interact cross-functionally with teams that include, but are not limited to Business Development and Quality Assurance, to ensure company milestones are met. This position will ensure that products are processed under GLP practices, with appropriate documentation in place, it will also interact with external customers for which samples are processed, assuring that such communication is clear and disseminated in time, and processed samples are shipped back to customer, according to customer timeline. | 12/01/2025 |
| 89 | Organogenesis Canton, MA Production Associate I - Apligraf (Sunday-Thursday) Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 12/01/2025 |
| 90 | Organogenesis Canton, MA QC Analyst I/II -Microbiology BS degree in a Microbiology or related field Exp: 1+ years |
Perform routine quality control microbiology activities in support of product production and releases. The position interacts with other internal departments, including Apligraf Production, PuraPly Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position may interact with external entities including contractors and suppliers. The QC Analyst I/II performs a wide variety of routine activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting result. | 12/01/2025 |
| 91 | Organogenesis Smithfield, RI Production Associate Dermagraft Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Dermagraft), under the direct supervision of the Dermagraft Team Leader/Dermagraft Supervisor/Manager. The Dermagraft Associate will support the Dermagraft Manufacturing department by performing the tasks that will assure the safe and timely processing of Dermagraft, working in both a ISO 7 and ISO 8 cleanrooms. | 12/01/2025 |
| 92 | Pace Analytical Oakdale, MN Experienced Pharma Analytical Chemist Bachelor's degree in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline Exp: 0-2 years |
The Scientist I will contribute to laboratory operations by performing analytical testing, interpreting data, and maintaining laboratory equipment and documentation in accordance with established protocols and quality standards. | 12/01/2025 |
| 93 | Pace Analytical Portsmouth, VA Analytical Chemist BS degree in Chemistry, Biology, Biochemistry, or a related degree Exp: 1-2 years |
A candidate for this role will support an organics laboratory in environmental services and equipment management. | 12/01/2025 |
| 94 | Pace Analytical Lebanon, NJ PLS QA Specialist I Bachelor's degree in chemistry, operations, or a closely related field Exp: 1-2 years |
Responsible for providing advanced oversight of the analysis and administration of various quality policies, programs, and practices in accordance with current Good Manufacturing Practices (cGMP); provides feedback, direction and guidance to employees and management, using advanced professional and technical knowledge of quality or related equipment, testing, and procedures. | 12/01/2025 |
| 95 | Pace Analytical Cleveland, OH Entry Level Chemical Regulatory Analyst Bachelor of Science (Chemistry, Engineering, or related field) Exp: 1-2 years |
This position is part of a team that gathers, analyzes, and reports packaging, post-consumer recycling, and plastic data to various government agencies, frequently through third party Producer Responsibility Organizations, in the US and Canada. The team is part of a larger group that supports regulatory and compliance activities. The candidate may also support activities of the larger group. Candidate will contact suppliers to request packaging data, collect the packaging information, and organize/format data for use in various reports. They will also review data collection and organization processes to document procedures for various activities of the group. For on-site materials that need physical weight determinations, they may need to work in a laboratory setting using appropriate measuring equipment to record weights. Candidate may also assist with Federal Plastics Registry reporting as needed. Organizational skills and the ability to work independently are required for this role. Skills related to data manipulation and the ability to use various Microsoft Office (and potentially other software applications such as Business Objects, MicroStrategies, OnBase, etc.) while working with large sets of data will be integral to the role. We are looking for a team player who is self-motivated, able to maintain high quality while handling repetitive tasks, and manage multiple projects for different stakeholders. | 12/01/2025 |
| 96 | Pall New Port Richey, FL Manufacturing Engineer Bachelor’s degree in Manufacturing, Mechanical, Industrial, Aerospace, or related Engineering field Exp: 1 year |
The Manufacturing Engineer is responsible for driving improvements across assigned value streams to meet Safety, Internal and External Quality, on-time delivery, lead time reduction, and Productivity. This role is a key part of the Value Stream leadership team, responsible for driving daily performance and leading data-driven, root-cause-based action plans to achieve breakthrough KPIs through LEAN (DBS) tools and continuous improvement. This position reports to the Operations Manager and is part of the Value Stream leadership team, located in New Port Richey, FL. It will be an on-site role. | 12/01/2025 |
| 97 | Parexel West Point, PA Scientist III - Analytical Chemist - High-Throughput Purification Support MS Degree in Chemistry, Biochemistry, or closely related field Exp: 1-2 years |
We are looking to fill a Scientist III – Analytical Chemist - High-Throughput Purification Support position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. | 12/01/2025 |
| 98 | Parexel West Point, PA Scientist III - Biophysical & Materials Analytical Characterization - FSP MS in chemistry, biology, or related field Exp: 1-2 years |
This is a laboratory-based scientific role in a fast-paced, multidisciplinary team environment, requiring the utilization of biophysical analytical characterization techniques to support development of vaccine drug substance and drug products in a GMP-like environment. The vaccine drug substance and product development support includes sample manipulation, equipment maintenance, routine analysis, and characterization of development vaccines to support process and formulation development. | 12/01/2025 |
| 99 | Parexel Rahway, NJ Scientist III - (HPLC) Chromatography - Separations & Molecular Biology - Immunoassay Experience - FSP MS Exp: 1-2 years |
Support of routine bioanalytical testing of samples from cell-line development, in-process, process development/characterization, forced degradation, release & stability, and pre-formulation. Other potential opportunities include method development/optimization, workflow optimization, and template development. | 12/01/2025 |
| 100 | Parexel Rahway, NJ Scientist II or III – Analytical Chemist Metrology Specialist B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline Exp: 1-2 years |
Metrology specialist is responsible for the oversight of regulated and non-regulated laboratory equipment. This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement. | 12/01/2025 |
| 101 | Parexel West Point, PA Scientist II or III - Metrology Specialist - FSP B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline Exp: 1-2 years |
The Metrology Specialist is responsible for the oversight of regulated and non-regulated laboratory equipment. This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement. | 12/01/2025 |
| 102 | Parexel Rahway, NJ Scientist III - Analytical Chemist - FSP MS degree Exp: 1-2 years |
We are looking to fill a Scientist 3 - Analytical Chemist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. | 12/01/2025 |
| 103 | Parexel West Point, PA Scientist III - Analytical Chemist - Drug Product MS degree Exp: 1-2 years |
We are looking to fill a Scientist 3 - Analytical Chemist - Drug Product position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. | 12/01/2025 |
| 104 | Parse Biosciences Seattle, WA Quality Control Associate I Bachelor’s degree in Molecular Biology, Biochemistry, or related biological sciences Exp: 6 months |
As a Quality Control (QC) Associate I, you will work as part of the Quality Control team to test and verify that all raw materials and finished goods meet defined specifications for quality, consistency, and performance. In this role, you will test our manufactured products against established standards and release criteria, ensuring our customers receive high-quality, conforming reagents. We are looking for candidates who are highly self-motivated, eager to expand their technical expertise, and committed to their team’s success in a fast-paced environment. | 12/01/2025 |
| 105 | PCI Bedford, NH QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 12/01/2025 |
| 106 | PCI Madison, WI QA Associate I - Operations Bachelor’s degree in a relevant scientific field Exp: 0-2 years |
Are you eager to build your career in pharmaceutical manufacturing while making a meaningful impact on product quality and patient safety? Join us at PCI as a Quality Associate I – Operations, where you’ll be on the front lines of GMP production—supporting real-time quality oversight, solving problems as they arise, and ensuring that every product meets the highest standards of safety, efficacy, and compliance. | 12/01/2025 |
| 107 | PCI Madison, WI QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 12/01/2025 |
| 108 | PCI Madison, WI Plant Engineer I BS in Chemical, Mechanical, or other Engineering degree Exp: 0-2 years |
The Plant Engineer I provides engineering support throughout the various manufacturing facilities in areas such as process equipment improvements, technological advancements, capital projects, existing manufacturing equipment, cost improvements, facility maintenance, safety and environmental regulation. Demonstrate good engineering, effective collaboration, partnering and teamwork skills when interacting with internal and external resources. | 12/01/2025 |
| 109 | PCI Philadelphia, PA Process Engineer Bachelor’s degree in mechanical, chemical, biomedical, packaging engineering, or a related field Exp: 1-5 years |
PCI is seeking a motivated and detail-oriented Process Engineer I to provide technical leadership in new product launches and continuous improvement initiatives. The ideal candidate will focus on mitigating packaging issues, optimizing production processes, and supporting operational efficiency. This role will involve providing technical and operational support to production, maintenance, and support teams, particularly in the areas of process improvement, equipment modification, optimization, safety, and quality improvement. The Process Engineer I will utilize lean and six sigma techniques and demonstrate excellent organizational and leadership skills in managing projects, equipment needs, staffing projections, and line layout. | 12/01/2025 |
| 110 | PCI Philadelphia, PA Facilities Engineer I Bachelor's Degree in a related field Exp: 1-5 years |
Facilities Engineer I estimates costs related to layout design, including equipment and materials, labor, etc. and monitors the construction process. Plans and implements the design of plants, offices, and production lines to maximize the use of available space and improve production efficiency. Ensure that established efficiency and safety targets are met. Research facilities equipment or fixtures for purchase and gather data relating to their ability to meet organizational needs. Works on projects/matters of limited complexity in a support role. Work is closely managed. | 12/01/2025 |
| 111 | PCI Rockford, IL Project Engineer- Drug Delivery Bachelor’s degree in Mechanical, Biomedical, Chemical, or related Engineering discipline Exp: 1-5 years |
As a Project Engineer – Drug Delivery, you’ll play a hands-on, critical role in the design, development, and execution of pharmaceutical packaging and assembly projects. Working closely with engineering, quality, and validation teams, you’ll help deliver high-impact solutions that directly affect patient outcomes around the world. This role supports key product introductions - including high-speed auto-injector lines for diabetes management—giving you the opportunity to work on cutting-edge drug delivery technology. You’ll collaborate with both internal stakeholders and external customers, ensuring projects are delivered on time, on budget, and in compliance with all regulatory standards. This is more than a role—it's a career path. Our Project Engineers have advanced to senior-level roles, including Engineering Manager, based on performance, innovation, and leadership. | 12/01/2025 |
| 112 | Penumbra Alameda, CA Manufacturing Engineer I - Electronics Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 12/01/2025 |
| 113 | Penumbra Alameda, CA Manufacturing Engineer II - Equipment Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, Industrial Engineering, or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. The Manufacturing Engineer Equipment II specializes in the design, development, evaluation, selection, and ordering of the equipment that is most appropriate and cost-effective for the manufacture of company products. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 12/01/2025 |
| 114 | Penumbra Alameda, CA Manufacturing Engineering Manager - Metals/Catheters Master’s degree in an engineering or related technical field Exp: 1+ years |
Provide management in the engineering, design and development of new products or changes to existing products, processes, and equipment. Direct the transfer and scale-up of products from R&D to Production. Exercise judgment within generally defined practices and policies in determining project plans (milestones, resources) and selecting methods and techniques for meeting project goals. | 12/01/2025 |
| 115 | Penumbra Alameda, CA Supplier Quality Engineer I Bachelor’s degree in engineering, science, or a related field Exp: 0-3 years |
As a Supplier Quality Engineer I at Penumbra, you will play a key role in ensuring our supply chain consistently delivers components and materials that meet the highest standards of quality and compliance. Working closely with cross-functional partners in Operations, Compliance, and R&D, you will support supplier qualifications, changes, corrective actions, and performance monitoring. You’ll help resolve supplier-related issues, drive improvements, and ensure adherence to Penumbra’s Quality Management System (QMS) and regulatory requirements. This is an excellent opportunity for an early-career engineer to build a strong foundation in supplier quality, gain exposure to medical device manufacturing, and grow within a high-impact quality organization. You’ll join a collaborative and growing Quality organization that invests in technical development and career growth. | 12/01/2025 |
| 116 | Penumbra Alameda, CA Quality Monitoring & Improvement Specialist I Bachelor's degree preferably in engineering, life sciences, or a related field Exp: 1+ years |
As a key member of the Quality team, you will have a hand in ensuring that Penumbra's life-saving products adhere to the highest standards of quality and safety. In the Quality Monitoring & Improvement Specialist I role, you will be supporting our Quality Management System (QMS) processes, specifically Corrective and Preventive Actions (CAPAs), Nonconformance Reports (NCRs) and Deviation Authorizations (DAs) following Penumbra's procedures and regulatory requirements. You will organize and host board meetings to facilitate board review of documentation supporting these systems. You will also assist with data compilation for monthly trending meetings. | 12/01/2025 |
| 117 | PerkinElmer Washington, DC Senior Project Engineer I, PF Services Bachelor’s Degree in Life Science, Engineering, or related discipline Exp: 1-2 years |
The Project Engineer is a fully billable role that will work collaboratively with clients, vendors, contractors, and other Team Members to support projects related to biomanufacturing across the entire engineering lifecycle. The Project Engineer is responsible for delivering high quality work, forming and maintaining valuable, long-term relationships with our clients, and continually strengthening their technical and industry knowledge. They will maintain a strong focus on Project Farma’s Patient Focused and People First mindset. | 12/01/2025 |
| 118 | Perrigo Eau Claire, WI Associate R&D Process Scientist Bachelor’s degree in Food or Dairy Science, Chemical or Food Engineering, Chemistry or closely related Exp: 1-3 years |
Perrig is currently hiring for an Associate R&D Process Scientist to lead scale-up of new infant formulas from development to full-scale production, overseeing change control, risk assessment, and factory trials while collaborating with cross-functional teams including Product Development, Pilot Plant, Operations, Quality, and Planning. Support manufacturing sites on continuous improvement opportunities in recipe and processing, driving optimization and renovation initiatives through root-cause analysis, cross-functional collaboration, and execution of cost-reduction strategies while ensuring compliance and operational excellence. Develop and implement new process capabilities via feasibility trials and continuous improvement projects to enhance efficiency, reduce costs, and improve overall product quality. | 12/01/2025 |
| 119 | Perrigo Bronx, NY QC chemist II - Days Bachelor of Science degree in a scientific discipline (Chemistry or Food Science preferred, Biology) Exp: 1-2 years |
To ensure the Quality and Compliance of raw materials, finished products, and stability samples by performing laboratory analytical testing relative to the support of Perrigo operations and manufacturing needs. Responsible for preparing solutions and reagents for testing as required. Uses analytical laboratory equipment such as HPLC, UPLC, GC, UV and IR. Works independently and within team under direction of supervisor to accomplish tasks. | 12/01/2025 |
| 120 | Personalis Fremont, CA Sample Accessioner 1 (Temp) Bachelor of Arts or Science Exp: 0-2 years |
This role offers the opportunity to gain experience in a fast paced cutting edge clinical lab environment. The Sample Accessioner will work in a team environment which includes project managers and clinical lab ops specialists. As an Accessioner, daily tasks will involve patient specimen intake, accessioning and fulfilling client requests for returns or destructions. This will entail following SOPs and working with Laboratory Information Management System (LIMS) and other software. This role will also perform shipping / receiving, recording and inventorying of samples sent for laboratory testing. | 12/01/2025 |
| 121 | Legend Biotech Raritan, NJ QC Technical Trainer III Bachelor’s Degree in Science, Engineering or equivalent technical discipline Exp: 0-2 years |
The QC Technical Trainer is an exempt level position working within QC Microbiology training team. This individual will be responsible for performing training activities for Quality Control Microbiology team members who support cGMP Clinical and Commercial Cell Therapy testing. This role will require technical experience, effective communication, coordination, and collaboration across relevant cross functional groups to enable robust testing and release of products to patients. This position is primarily a M-F schedule, with potential nights or weekends temporary coverage as needed. | 11/24/2025 |
| 122 | Legend Biotech Somerset, NJ Associate Scientist Bachelor’s degree in biotechnology, Bioengineering, Molecular Biology, or related discipline Exp: 1-2 years |
We are seeking a motivated Associate Scientist to join our MSAT team, supporting the development, troubleshooting, and optimization of automated manufacturing processes for CAR-T and other cell therapy products. Under the guidance of senior staff, this role will perform bio-pilot run experiments, technology evaluations, and process improvement studies. The position will directly contribute to manufacturing robustness and efficiency by executing laboratory work, assisting in equipment testing, and analyzing process data. | 11/24/2025 |
| 123 | Legend Biotech Raritan, NJ Operations Associate Bachelors Degree required in Life Sciences Exp: 0-2 years |
This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations. | 11/24/2025 |
| 124 | Legend Biotech Raritan, NJ QC Analyst I Bachelor’s Degree in Science, Engineering or equivalent technical discipline Exp: 1 year |
The QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. | 11/24/2025 |
| 125 | Legend Biotech Somerset, NJ Senior Research Associate/Associate Scientist (Contractor) MS in Biology or related field Exp: 1+ years |
We are seeking a highly motivated and detail-oriented Bioassay research scientist to join our Bioanalytical team. The ideal candidate will bring technical expertise in molecular assays (qPCR/ddPCR), multi-parameter flow cytometry and contribute to the daily operations of the lab supporting both clinical and preclinical research. This role requires strong organizational skills, the ability to collaborate effectively with cross-functional teams, and a background in biology or a related field. The successful candidate will play a critical role in ensuring the accuracy, reproducibility, and integrity of experimental data. | 11/24/2025 |
| 126 | LGC Petaluma, CA Oligo Manufacturing Technician I Bachelor's degree in a related field Exp: 1 year |
The Oligo Manufacturing Technician I is responsible for supporting Molecular Biology Conversion manufacturing in an ISO 9001 (Custom RUO) and/or ISO 13485 (DxGMP) regulated environment. This position performs production procedures in compliance with current Good Manufacturing Practices (cGMP) (ISO 13485), Standard Operating Procedures (SOPs), and applicable regulatory standards. The technician will work closely with cross-functional teams to deliver high-quality oligonucleotide products for research or diagnostic applications. | 11/24/2025 |
| 127 | LGC Petaluma, CA Chemistry Technician I/II Bachelor’s Degree in a Physical Science Exp: 0-2 years |
This role is responsible for the manufacturing of Controlled Pored Glass (CPG) materials by following established and robust protocols. This position will primarily work with solid phase chemistry that is used in oligo manufacturing. CPG material manufacturing includes amine and nucleoside modification of native CPG at various angstrom sizes as well as modification with proprietary dyes and quenchers. The Chemist I will also be responsible for the upkeep of basic CPG equipment used in these processes. | 11/24/2025 |
| 128 | LGM Pharma Rosenberg, TX Quality Assurance Specialist Bachelor’s degree in a scientific discipline or equivalent Exp: 1+ years |
Performs initial, in-process and final inspections during manufacturing/packaging of product; resolves inspection findings with Packaging Manager and/or QA Manager. Collects product samples for product release testing, process validation testing and product stability as applicable and prepare labels at completion of packaging. Prepares documentation and forward samples to QC Lab for required testing; records information on batches in-process of testing on QC board; notifying QC of any urgent testing. Monitors incoming materials as received in Quarantine. Reviews material received paperwork and compare to material received for accuracy; notifying Materials Department to call supplier if CofA has not been received or CofA is incomplete. Coordinates with production areas to anticipate material usage to meet required schedule. Prepares required approval documentation for component or raw material inspection or testing. Collects raw material samples, label and forward with appropriate documentation to QC lab. Reviews lab data and approve/reject raw materials for use in production. | 11/24/2025 |
| 129 | Locus Biosciences Morrisville, NC Associate Quality Specialist Bachelor’s Degree in Biology, Chemistry, Life Sciences or Engineering Exp: 1 year |
Locus Biosciences is seeking a full-time Associate Quality Specialist. This individual will directly report to the Associate Director of Quality and will be responsible for leading, supporting and ensuring continued suitability of the Quality Management System (QMS) with a primary focus on design control, validation, risk management, supplier management, process control, post-market surveillance, complaint handling, CAPA, auditing, change control, document control and training. | 11/24/2025 |
| 130 | Lubrizol Brecksville, OH Laboratory Specialist Bachelor’s Degree in Engineering or related technical discipline Exp: 1+ years |
As a Technical Specialist, you will be an integral part of our dynamic R&D Laboratory. The ideal candidate will possess the ability to work collaboratively with our scientists and engineers to address and resolve a diverse range of technical challenges. The successful candidate will exemplify a strong commitment to the safe and efficient operation of our laboratories, which encompass both thermal processing equipment and sensitive analytical instruments. | 11/24/2025 |
| 131 | Lumos Pharma Remote, Clinical Quality Assurance Specialist Bachelor's Degree in Biology, Chemistry, Health Administration, or related technical discipline Exp: 1-3 years |
This position reports to the Vice President, Quality and Compliance, and is responsible for providing quality oversight of clinical trial activities performed in compliance with Good Clinical Practices (GCP). This position also supports internal quality systems and compliance functions. The Clinical Quality Assurance Specialist is expected to execute established processes involving quality assurance, quality systems, and compliance. | 11/24/2025 |
| 132 | MannKind Danbury, CT Engineer II, Validation MS in a technical discipline Exp: 1-3 years |
The Engineer II, Validation understands validation methodology and can apply it to process, packaging, equipment, and cleaning activities. Generates and executes validation protocols with limited supervision. Adheres to validation schedules. | 11/24/2025 |
| 133 | MannKind Danbury, CT Specialist I, Quality Assurance BA/BS degree in a scientific or technical discipline Exp: 1-2 years |
Ensures processes and products conform to established company and regulatory standards. Reviews, analyzes and reports on quality discrepancies related to manufacturing and testing of product and company systems. Investigates problems and recommends disposition and corrective actions for recurring discrepancies. Uses predetermined methods, operations and procedures to inspect and test raw materials, work-in-process, finished product as applicable. | 11/24/2025 |
| 134 | Mariana Oncology Watertown, MA SRA I/II, Bioanalytical Sciences Master’s degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or relevant scientific discipline Exp: 1+ years |
We are seeking an experienced Senior Research Associate I/II, Bioanalytical Sciences to join Mariana’s Preclinical Development organization, advancing personalized medicine and radiopharmaceuticals. This laboratory-based position will play a key role in conducting LC-MS-based bioanalysis to support pharmacokinetic (PK), in vitro ADME, and proteomics studies across preclinical programs, focusing on sample preparation, method execution, and data collection. The successful candidate will contribute directly to the development of novel therapeutics by generating high-quality quantitative and qualitative bioanalytical data. | 11/24/2025 |
| 135 | Masimo Irvine, CA Operations Analyst Bachelor’s degree, preferably in Engineering related fields Exp: 1-3 years |
The Operations Analyst will play a key role in enabling the company’s Operations to function by leveraging state of the art processes, tools, and methods. | 11/24/2025 |
| 136 | Matica Bio College Station, TX Validation Engineer I Bachelor`s Degree in a Life Science, Engineering or related science discipline Exp: 1-2 years |
The Validation Engineer I is an entry level position and will support the efforts of the Validation department. | 11/24/2025 |
| 137 | Meissner Camarillo, CA Associate Scientist I Bachelor's degree (BS) in chemistry, biology, or related subject Exp: No exp |
The Associate Scientist I, under direct supervision, supports laboratory testing activities focused on pharmaceutical filtration and analytical studies. This role involves performing routine tests as well as conducting analytical tests. The role includes maintaining laboratory equipment, records, and cleanliness, while adhering to established procedures and safety protocols. | 11/24/2025 |
| 138 | Merck Elkhorn, NE Quality Control Technician Bachelor's degree in a technical scientific discipline Exp: 1+ years |
Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products. | 11/24/2025 |
| 139 | Microbiologics Saint Cloud, MN Manufacturing Science Associate Bachelor’s degree in a relevant field (e.g., Biology, Microbiology, Molecular Biology, or related discipline) Exp: 1-3 years |
We are looking to add two (2) Manufacturing Science Associate's to our R&D Team in St. Cloud, MN. In this role the Manufacturing Science Associate will be supporting the development, validation, and continuous improvement of manufacturing processes throughout the product lifecycle. This role bridges research and production—transforming innovative product designs into scalable, high-quality manufacturing processes. The ideal candidate will apply scientific and technical expertise to drive efficiency, ensure compliance, and uphold rigorous documentation and integrity standards. | 11/24/2025 |
| 140 | MilliporeSigma Bedford, MA Scientist 1 - Analytical Chemistry Bachelor’s or Master's degree in Chemistry, Biology, Chemical Engineering, Biomedical Engineering or other Science or Engineering field Exp: 1+ years |
Join our team at MilliporeSigma as a Scientist 1 in Bedford, MA. In this role, you will be part of the Analytical team that focuses on the development, optimization and performance of analytical methodology supporting research and development of new products and their manufacturing processes. Your role will be to perform extractables studies, and to determine compounds that can be released or migrate from single-use and filtration devices and other MilliporeSigma products, using TOC, HPLC, GCMS, ICP, ion chromatography, LCMS, and other appropriate characterization techniques. This role will be lab-based, driving projects forward through innovation. | 11/24/2025 |
| 141 | MilliporeSigma Jaffrey, NH Project Management Engineer Master of Science Degree in Plastics Engineering, Biomedical Engineering, or other Engineering discipline Exp: 1+ years |
Join our team as a Project Management Engineer, where you'll take the lead on exciting projects focused on validating new, repaired, and transferred injection molds. In this role, you will be responsible for building the justification, scope, and budget necessary to support investments in the fabrication or repair of injection molds and related equipment. Proactively maintain outsourced injection molds by providing guidance to suppliers and ensuring internal quality/supply standards are met. | 11/24/2025 |
| 142 | MilliporeSigma Lenexa, KS Process Engineer Bachelor’s degree in Chemical Engineering, Bioprocess Engineering, or related Engineering Discipline Exp: 1+ years |
Primary responsibility is to monitor and support the Dry Powder Manufacturing process in Lenexa, KS. It is a 24/7 media manufacturing plant which requires round the clock support. The position is responsible for understanding the Dry Powder Media manufacturing process to include blending, pin milling, dispensing/packaging, and the cleaning/drying of the equipment. The incumbent will navigate the process control systems for the equipment and understand how the system interfaces and stores data to OSI PI historian. The engineer will have knowledge of product powder attributes such as particle size, bulk density, flowability, and cohesiveness. The process engineer is the liaison between maintenance, engineering, and the shop floor. Provide support and mentoring to other engineering and engineering support personnel. Assist operations implementation of process improvements and during equipment startup and commissioning activities. | 11/24/2025 |
| 143 | MilliporeSigma St. Louis, MO Quality Assurance Product Release Analyst Bachelor’s Degree in a scientific (Biology, Chemistry, etc.) discipline Exp: 1+ years |
The Quality Assurance Product Release Analyst plays a role in ensuring the timely release of purchased and produced goods. This position is responsible for performing a variety of quality review functions according to established criteria and guaranteeing that products meet all necessary specifications. | 11/24/2025 |
| 144 | MilliporeSigma Bellefonte, PA Associate Production Scientist Bachelor’s degree in Chemistry, Biochemistry, Biology, Chemical Engineering or other Life Science field Exp: 1+ years |
MilliporeSigma in Bellefonte, PA is seeking an Associate Production Scientist. In this role you will manufacture or evaluate gas chromatographic (GC) capillary products according to established protocols, provide technical support to others, and perform operations in support of the group and department. | 11/24/2025 |
| 145 | MilliporeSigma Bedford, MA Scientist 1 - Chemistry Bachelor’s degree Exp: 6+ months |
MilliporeSigma in Bedford, MA is seeking a Scientist 1. The Scientist 1 within the Filtration Research and Development department will assist in the design, development, and testing of novel filtration products/technologies suitable for the manufacture of therapeutic biopharmaceuticals. | 11/24/2025 |
| 146 | MilliporeSigma Indianapolis, IN Microbiology Analyst 2 Bachelor’s Degree in Biology, Immunology, Biochemistry or other Science or Medical discipline Exp: 1+ years |
You will help ensure our manufacturing areas are meeting all pharmaceutical standards, including our aseptic environment. You will assist with collecting samples on critical utilities such as nitrogen, process air and the sites’ water systems. You will help with performing media fills including qualification and release in support of the environmental monitoring program. You will help with maintaining equipment and adhering to the sites Environmental Health and Safety program. You will assist with routine lab-related tasks and ensuring your work area is tidy to support audit readiness and bring issues to supervision immediately for escalations. You will also support QC in-process testing as a backup for weekend work. | 11/24/2025 |
| 147 | Modulo Bio San Diego, CA Stem Cell Scientist MS in Genetics, Molecular Biology, Developmental Biology, Biochemistry, Regenerative Medicine, Neuroscience, or related field Exp: 1+ years |
Modulo Bio is seeking a Stem Cell Scientist to develop and scale an induced-pluripotent stem cell (iPSC)-based in vitro model of the neuroimmune system. Modulo Bio is building a proprietary immune cell modeling platform, which incorporates human genetics, functional genomics, molecular biology, cellular and tissue profiling, disease model engineering, and advanced computational models. The successful candidate will build a complex cell model platform with the goal of improving our understanding of human biology and therapeutic interventions to inform early and late stage pipeline efforts. Candidates with an eagerness to work within a highly leveraged, team-driven, dynamic research environment will be prioritized. The candidate will work in close collaboration with our internal Computational Biology group which is focused on next-generation sequencing (NGS), functional genomics, cell or tissue profiling, and bioinformatics analyses of cutting-edge large-scale genetic screening or single-cell technologies to enhance our analytic capabilities and to reveal the underlying mechanisms of human disease. | 11/24/2025 |
| 148 | Moog Buffalo, NY Associate Product Engineer Bachelor of Science in Mechanical or Electrical Engineering, or comparable field of technology Exp: 0-2 years |
As an Associate Product Engineer, with Moog Aircraft Group’s Electronics Operations Engineering Team, you will be assigned direct engineering responsibility for a variety of production programs. Work assignments require some originality and unreviewed action. You will receive program and technical guidance from the department supervisory personnel, project, senior product, or product engineers. | 11/24/2025 |
| 149 | Moog Buffalo, NY Project Engineer, Test Equipment MS Degree in Engineering Exp: 1 year |
As a Project Engineer, Test Equipment in our Space & Defense Group in East Aurora, NY you will be responsible for design and development of hydraulic, electro-hydraulic, electro-mechanical, servo-mechanism, and electro-pneumatic components and systems that will be used to test the products of Moog, Inc. | 11/24/2025 |
| 150 | Moog Buffalo, NY Electronics Development Engineer BS degree in Electrical Engineering Exp: 1 year |
The Commercial Aircraft Electronics Group is looking for an Electronics Development Engineer to be responsible for the development and sustainment of Flight Control Computers (FCCs), Actuator Control Units (ACUs), and Motor Control Electronics (MCEs) for primary and secondary control systems for commercial aircraft. | 11/24/2025 |
| 151 | NAMSA Irvine, CA Laboratory Technician - Quality Control Bachelors degree Exp: 0 years |
Clean glassware and prepare reagents for use in laboratory testing. Perform routine disposal of laboratory waste including disposal of test articles. Assist with making solutions and preparing reagents. Assist in the preparation of items for testing. May be involved in various testing activities in accordance with SOPs, applicable work instructions. Review raw materials and final finished media for conformance with applicable material specifications and SOPs. May be responsible for extractions, test article and control preparation, animal holding and preparation and solution preparation. May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. Accurately collect and record raw data in logbooks and on worksheets. Maintain clean workspace, testing supplies, and equipment. May be responsible for checking laboratory equipment, being on-call and responding to continuous monitoring alarms in accordance with criteria outlined in Standard Operating Procedures. May be required to operate specified laboratory equipment. Other duties as assigned. | 11/24/2025 |
| 152 | NAMSA Atlanta, GA Microbiology Technologist Bachelor's degree Exp: No exp |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform required specific testing as applicable. May be required to operate specified laboratory equipment. May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable). Other duties as assigned. | 11/24/2025 |
| 153 | Natera San Carlos, CA QC Reagent Associate I BS/BA degree in Biological Sciences, Biology, Chemistry or a related field Exp: 1+ years |
Support the activities for reagents used in the Operations Department’s Clinical Laboratories. Executes the preparation and qualification of molecular diagnostic reagents. Performs Quality Control tests on new incoming shipments of raw materials and small-scale manufacturing procedures (formulations and dispensing) reagent. Reviews data obtained for compliance to specifications and reports abnormalities. Maintains and improves QC documentation pertaining to raw material specification, reagent qualification, and QC testing. Support Incoming Quality Control activities as needed. | 11/24/2025 |
| 154 | Natera San Carlos, CA Lab Associate Bachelor’s degree in life-science or related field Exp: 1 year |
The Lab Associate supports R&D labs by ordering, receiving, and storing reagents and materials. Upkeeps laboratory consumables and reagents inventory. Fulfills various requests by research staff related to laboratory workflows and anticipate laboratory needs. | 11/24/2025 |
| 155 | Natera San Carlos, CA Research Associate 1 BS/BA in a biological science or equivalent Exp: 1-2 years |
The Research Associate 1 performs laboratory procedures of varying complexity contributing to cross functional activities as part of the Oncology Team, a multidisciplinary team within the research and development department. | 11/24/2025 |
| 156 | Neuropace Mountain View, CA Manufacturing Engineer BS degree in mechanical or manufacturing engineering Exp: 1-2 years |
We are currently seeking a Manufacturing Engineer to join our team at NeuroPace. The Manufacturing Engineer will support the development, documentation, verification, and ongoing manufacturing of products and processes required to produce an implantable Neuro-Stimulator and supporting lead systems. | 11/24/2025 |
| 157 | NewLimit South San Francisco, CA Vivarium Technician Bachelor’s degree (B.A./B.S) in animal or life sciences field Exp: 1 year |
NewLimit is seeking a Vivarium Technician with experience in rodent husbandry and in vivo technical procedures. In this role, you will help support vivarium operations, animal husbandry, and in vivo research in collaboration with New Limit’s product teams to test reprogramming medicines in pre-clinical rodent models. | 11/24/2025 |
| 158 | NextPhase Mansfield, MA Quality Engineer Bachelor’s Degree in Engineering, Quality Assurance or related Exp: 1+ year |
The Quality Engineer will support the Quality Management System (QMS) to ensure compliance to FDA Quality System Regulation, ISO 13485 and other relevant Quality System Standards. The Quality Engineer will also participate in product development teams to provide design control quality assurance support to medical device development and validation efforts. | 11/24/2025 |
| 159 | Nordson Duluth, GA Electrical Engineer I Bachelor’s degree in electrical engineering or computer engineering Exp: 0-3 years |
The Electrical Engineer drives continual improvement in product quality for Nordson. They serve as the primary engineering contact for our global field and sales teams. They are responsible for maintaining communication between the field, manufacturing, and product development engineering relative to customer concerns and quality issues. The EE owns the Corrective Action Request process and ensures a data driven approach is executed to yield qualified corrective actions. This position interfaces with sales, purchasing, factory assembly and planning teams, machine shop, external vendors, and other engineering organizations within Nordson. | 11/24/2025 |
| 160 | Nortech Bemidji, MN Quality Engineer Bachelor’s degree in engineering, quality, or closely related subject Exp: 1 year |
Work with manufacturing and engineering to ensure clear documentation, interpretation, and inclusion of customer requirements for assigned products. Support, plan, and implement activities concerned with development, application, and maintenance of quality standards for manufacturing processes, materials, products, and/or business systems. Develop, implement, and support standards and methods for inspection, testing, and evaluation relative to Nortech’s quality management standards to ensure products leaving the manufacturing or development organization are effective and free from defects or operational problems or errors. Review product, component, part, and assembly specifications, and develop and/or update testing-related documentation including test cases, plans, and flaw-reporting procedures. Work with training staff to ensure production and inspection personnel are properly trained. Support quality related issues such as interpretation of workmanship standards, manufacturing processes, customer prints, specifications and defect evaluations. Devise sampling procedures, design and develop forms and instructions for recording, evaluating, and reporting quality data. Develop and implement methods to ensure compliance of product development, documentation, manufacturing, and assembly processes. Maintain applicable quality records and perform quality audits in accordance with established standards. Compile, calculate, maintain, and report summary statistics required by customers. Inform product conformance decisions based on interpretation of quality data reports, SPC charts, and other applicable data; promptly notify management of concerns with potential to impact product volume, manufacturing lines, costs, or customer outcomes. Work with suppliers, customers, and internal departments on obtaining and/or responding to deficiencies and/or corrective actions. Coordinate the successful closure of closed loop corrective actions concerning quality issues of products and processes. Keep supervisor informed about project status, workload, concerns, questions, and progress. Demonstrate and support Nortech’s Mission, Core Values, policies and procedures at all times. May perform other duties and responsibilities as assigned. | 11/24/2025 |
| 161 | GRAM Grand Rapids, MI QC Microbiology Technician Bachelor’s degree in Microbiology or a related field Exp: 0-2 years |
The QC Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. The hours for this role are Fri-Sun, 6:00 am-6:00 pm. | 11/18/2025 |
| 162 | Flagship Labs Cambridge, MA Research Associate, Protein Degradation Master’s degree in Biochemistry, Cell Biology, Molecular Biology, or a related discipline Exp: 0+ years |
We are seeking a highly creative, resourceful, and motivated Research associate to join our Protein degradation team. The ideal candidate will help us set up our in-house protein production capabilities and support our cell-culture and molecular biology efforts. Strong candidates will be independent, goal-oriented, and have excellent communication skills. We are seeking individuals who can be highly adaptable and comfortable working in a dynamic and fast-paced collaborative and multidisciplinary environment. This is a unique opportunity to drive the growth of an early-stage biotechnology company where you can meaningfully define the next frontier of protein homeostasis modulators. The successful candidate will play a key role in driving our discovery efforts aimed at developing therapeutic strategies that modulate protein homeostasis. | 11/18/2025 |
| 163 | Flagship Labs Cambridge, MA Senior Research Associate, Analytical Development M.S. in Analytical Chemistry, Chemistry, Biochemistry, Chemical Engineering, or related field Exp: 1+ years |
We are searching for an experienced and enthusiastic Senior Research Associate (SRA) to contribute to the method development and characterization of novel nucleic acid therapeutics. We are looking for an individual who enjoys hands-on laboratory benchwork and brings scientific rigor and intellectual curiosity to their role. This individual will have the opportunity to work in a dynamic and fast-paced entrepreneurial environment as part of a highly collaborative and rapidly growing team. | 11/18/2025 |
| 164 | Helix San Diego, CA Lab Aide Bachelor’s degree in laboratory science or medical laboratory technology Exp: 0-1 years |
Join Helix's world-class, high-volume CAP/CLIA certified laboratory where transforming health organizations by weaving genomics into the fabric of healthcare. As a Lab Aide, you'll be at the forefront of our pre-analytical operations, working with a dynamic team that processes thousands of patient specimens daily. This role offers unique opportunities to challenge industry standards through innovative solutions. You'll gain hands-on clinical laboratory experience in a state-of-the-art facility while supporting the accessioning activities, plating procedures, and biohazardous waste program. With clear advancement pathways, you'll have the opportunity to grow from executing foundational tasks to becoming a subject matter expert and leader within the laboratory operations team. | 11/18/2025 |
| 165 | HighRes Biosolutions Beverly, MA Field Service Engineer I Bachelor’s degree in electromechanical/life science/engineering Exp: 0-3 years |
The Field Service Engineer position at HighRes Biosolutions is the primary role responsible for installation, maintenance, troubleshooting and repair of systems and devices at customer sites. This position is specialized on the hardware aspect of the products, coordinating with the Automation Support Engineer role in Customer Support and collaborating with the manufacturing and commissioning department (software and configuration-focused) for full coverage support of the products. Levels I and Junior are roles for carrying out Field Service Engineer responsibilities in either learning or assisted modes, with oversight and assistance from a team lead, supervisor, manager, or skilled technical Customer Service colleague(s). | 11/18/2025 |
| 166 | Hologic Newark, DE Senior Electrical Engineer Master’s degree in Electrical Engineering or related technical field Exp: 1-3 years |
As a Senior Electrical Engineer, you will design, develop, and evaluate electrical components and processes for our innovative breast and skeletal health products. You’ll be responsible for the physical layout of printed circuit boards, translating electronic schematics into reliable, manufacturable board designs, and ensuring compliance with performance and regulatory standards. | 11/18/2025 |
| 167 | Hologic Newark, DE Senior Quality Assurance Engineer Master's Degree in Electrical Engineering Exp: 1-3 years |
Are you a quality-focused professional passionate about ensuring excellence in manufacturing and production processes? Join Hologic as a Senior Quality Assurance Engineer and play a critical role in designing, implementing, and maintaining quality assurance protocols that meet internal and external regulatory standards for worldwide distribution. In this role, you’ll collaborate with cross-functional teams, lead quality initiatives, and drive continuous improvement to ensure the delivery of high-quality, innovative products that improve lives globally | 11/18/2025 |
| 168 | Hologic Newark, DE Quality Assurance Engineer Bachelor’s Degree Exp: 0-2 years |
Are you passionate about ensuring the safety, reliability, and compliance of life-saving medical devices? At Hologic, we are seeking a Quality Engineer to support the design, manufacturing, and quality assurance of medical devices. In this role, you will apply quality protocols, perform inspections, investigate non-conformances, and drive continuous improvement initiatives to uphold our commitment to excellence. If you’re detail-oriented, eager to learn, and ready to contribute to a team focused on delivering high-quality products, we encourage you to apply and be part of our mission to improve lives worldwide. | 11/18/2025 |
| 169 | Hologic Newark, DE Electrical Engineer 2 Bachelor’s or Master's Degree Exp: 0-2 years |
The Electrical Engineer designs, develops, modifies and evaluates components and processes used in the generation, manipulation, transmission and storage of electricity. Determines design approaches and parameters. Analyzes equipment to establish operating data, conducts experimental tests and evaluates results. Selects components and equipment based on analysis of specifications and reliability. Completes documentation and procedures for installation and maintenance. May interact with users to define system requirements and/or necessary modifications. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise. A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is a fully qualified, career-oriented, journey-level position. Normally receives little instruction on day-to-day work, general instructions on new assignments. | 11/18/2025 |
| 170 | Hologic Newark, DE Electrical Engineer 3 Bachelor’s or Master's Degree Exp: 0-3 years |
The Electrical Engineer designs, develops, modifies and evaluates components and processes used in the generation, manipulation, transmission and storage of electricity. Determines design approaches and parameters. Analyzes equipment to establish operating data, conducts experimental tests and evaluates results. Selects components and equipment based on analysis of specifications and reliability. Completes documentation and procedures for installation and maintenance. May interact with users to define system requirements and/or necessary modifications. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise. A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is a fully qualified, career-oriented, journey-level position. Normally receives little instruction on day-to-day work, general instructions on new assignments. | 11/18/2025 |
| 171 | Hologic San Diego, CA Scientist 2 - Post-Market Investigations Master’s in Chemistry, Biochemistry, Molecular Biology, Biomedical Engineering, or related scientific discipline Exp: 1-3 years |
We are hiring a highly motivated Scientist 2 in our Diagnostic division, Quality Technical Investigations (QTI) team. In this role and under QA function, you will coordinate and lead high complexity investigations related to customer complaints for assay reagents in Hologic's quality management system and moderate/high complexity projects in support of compliance and overall Hologic continuous improvement efforts. The incumbent will provide Technical Subject Matter Expertise (SME) to all levels of staff including QTI team as well as advising leadership as required. You may be responsible for communicating complex information to the key stake holders for effective decision making. When needed you may be responsible for performing laboratory hands on work to support QTI team’s projects, tasks etc. | 11/18/2025 |
| 172 | Hyperfine Guilford, CT Regulatory Affairs Associate Bachelor’s degree in a scientific or regulatory discipline Exp: 1 year |
As our Regulatory Affairs Associate, you will be an individual contributor responsible for analysis, evaluation, preparation, and submission of documentation for regulatory approval, ensuring Hyperfine products and procedures comply with US and global regulatory specifications. You will support our Regulatory team across different program areas, and will work on multiple projects concurrently. | 11/18/2025 |
| 173 | INCOG BioPharma Fishers, IN Filling Prep Specialist BS in biological sciences/biotechnology or related field Exp: 1 year |
The Filling Prep Specialist’s primary responsibility is to efficiently and safely set up and operate the various pieces of production equipment within the facility. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should possess a strong mechanical aptitude with strong trouble shooting skills on manufacturing equipment. They should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and inspire problem solving & solution driven thinking. | 11/18/2025 |
| 174 | INCOG BioPharma Fishers, IN Formulation Specialist BS in biological sciences/ biotechnology Exp: 1+ years |
The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 11/18/2025 |
| 175 | INCOG BioPharma Fishers, IN Manufacturing Specialist BS in biological sciences/biotechnology or related field Exp: 1 year |
The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 11/18/2025 |
| 176 | INCOG BioPharma Fishers, IN Tech Transfer Engineer Bachelors’ or Masters' degree in Science or Engineering Exp: 1-3 years |
The Technical Services and Manufacturing Sciences (TSMS) Technical Transfer Engineer will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the production to ensure robust and reliable production processes are established. | 11/18/2025 |
| 177 | INCOG BioPharma Fishers, IN TSMS Engineer Bachelors’ or Masters' degree in Science or Engineering Exp: 1-3 years |
The Technical Services and Manufacturing Sciences (TSMS) Technical Transfer Engineer will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the production to ensure robust and reliable production processes are established. | 11/18/2025 |
| 178 | INCOG BioPharma Fishers, IN TSMS Operations Engineer Bachelor's degree in Science or Engineering Exp: 1-2 years |
The Technical Services and Manufacturing Sciences (TSMS) Operations Engineer will provide direct technical support to manufacturing operations on the production floor in accordance with current good manufacturing practices (cGMP) for clinical and commercial programs. This role will work closely with manufacturing operators and supervisors to ensure smooth production operations, troubleshoot technical issues, and support process execution as specified. | 11/18/2025 |
| 179 | Indivior Raleigh, NC MQA Specialist - 2nd Shift Bachelor’s degree in science, engineering field Exp: 1 year |
The Manufacturing Quality Assurance (MQA) Specialist – 2nd Shift is responsible for providing quality oversight to all manufacturing areas to ensure product quality and SOP/GMP compliance. The MQA Specialist will work closely with production personnel to complete in-process batch record review, resolve batch related issues, and ensure proper good documentation practices. In addition, the MQA Specialist will be responsible for performing routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 11/18/2025 |
| 180 | Indivior Raleigh, NC Environmental Monitoring Technician Bachelor’s degree in Chemistry, Microbiology, Biology or other related Science Exp: 1 year |
The purpose of the EM Technician I is to perform routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 11/18/2025 |
| 181 | Insmed San Diego, CA Senior Research Associate, Quality Control Master’s degree in relevant discipline Exp: 0 years |
We’re looking for a Senior Research Associate, Quality Control to help us expand what’s possible for patients with serious diseases. Reporting to the Associate Director, Quality Control, you’ll be involved in transfer of method from Analytical Development into QC. The Quality Control Senior Research Associate will author and execute phase appropriate qualification/validation protocols and reports of QC methods to support product release, stability, and characterization. The role will perform analytical and biochemical analysis on lot release, stability, and process characterization samples to support Insmed AAV Gene Therapy products. | 11/18/2025 |
| 182 | Integer Plymouth, MN Process Development Engineer I Bachelor’s degree in an engineering or related technical field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves general engineering methods and tools. As an entry level engineer, you will ensure that Integer’s internal and external customer expectations are met or exceeded with the direction, instruction and guidance from more experienced engineers and managers in your organization. | 11/18/2025 |
| 183 | Integer Palm Harbor, FL Design Assurance Engineer I Bachelor’s degree in a related field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves conventional engineering practice. Ensures Integer’s internal and external customer expectations are met or exceeded. Initiates, directs and manages the design, development, constructing and modification of products and processes from conception to implementation. Works closely with other departments to coordinate design engineering activities. Reviews, initiates or approves engineering drawings, layouts, changes orders and specifications | 11/18/2025 |
| 184 | Integer Plymouth, MN R&D Engineer I Bachelor’s degree in an engineering or related technical field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves general engineering methods and tools. As an entry level engineer, you will ensure that Integer’s internal and external customer expectations are met or exceeded with the direction, instruction and guidance from more experienced engineers and managers in your organization. | 11/18/2025 |
| 185 | Integra LifeSciences Braintree, MA Quality Engineer II - Design & Reliability Assurance Master’s degree in science, Engineering (Biomedical or Mechanical) Exp: 0-2 years |
The Quality Design and Reliability Assurance (DRA) Engineer II is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, specifically the Boston/ Braintree site. The role contributes and supports the design and development of new and improved products. The (DRA) Engineer II will interact with external design and development partners, participating on cross-functional project teams through all phases of the product development process, and assisting the technical team with planning, executing, documenting, and communicating testing activities. The role works with Product Development, Project Management, Regulatory, Marketing and Medical Affairs. | 11/18/2025 |
| 186 | Iovance Philadelphia, PA Process Development Associate I Bachelor’s degree (B.S./B.A.) in a life science or STEM-related discipline Exp: 1+ years |
The Process Development Associate I will provide process and analytical support to Tumor Infiltrating Lymphocyte (TIL) clinical and commercial development projects as part of the late-stage process development team. The successful candidate will have prior cell culture, process or method development, and cGLP/cGMP knowledge and experience. This role is a lab-based position, based in the Iovance Cell Therapy Center (iCTC) in Philadelphia, PA. | 11/18/2025 |
| 187 | Johnson & Johnson Danvers, MA Design Quality Engineer Bachelor’s degree in engineering or scientific discipline Exp: 1+ years |
The ideal candidate for the Design Quality Engineer position will support various New Product Development and sustaining activities as well as play a role in product risk management, cybersecurity, change controls, and design controls. This engineer should excel in an environment that embraces teamwork, change, risk-based decision-making and flexibility. Be ready to make a significant contribution to a dynamic, fun, multi-disciplinary team, where a self-motivated engineer with excellent written and verbal communication skills stands ready to succeed. | 11/18/2025 |
| 188 | Johnson & Johnson Raritan, NJ CAR-T Manufacturing Operator Bachelor’s degree required in Life Sciences or Engineering Exp: 0-2 years |
This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment. This position is responsible for the quality and maintaining the highest standards in compliance with company policies, procedures, and all applicable regulations. Responsible for fostering site pride and J&J citizenship. | 11/18/2025 |
| 189 | Jubilant HollisterStier Spokane, WA Process Engineer I Bachelor’s of Arts or Science with a major in Biology, Chemistry, Physics, or Engineering Exp: 0-5 years |
The Process Engineer I/II/IIIprovides ownership and focus for pharmaceutical processes and technical transfers at Jubilant HollisterStier. This position will engage in and manage projects and multi-disciplinary teams with direct supervision. The process engineer will also contribute technical direction for complex projects and exhibit clear communication skills with all levels of employees. | 11/18/2025 |
| 190 | KBI Durham, NC Manufacturing Associate I Bachelor's degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II will perform Upstream or Downstream production activities for early and late-phase Cell Culture programs in a GMP environment. Responsibilities include executing tasks per SOPs, batch records, and GMP/GDP/GLP standards, ensuring compliance and accuracy. The role involves various unit operations such as media/buffer preparation, bioreactor operations, aseptic techniques, chromatography, ultrafiltration, and drug substance filling. Candidates must maintain process ownership, facility upkeep, and thorough documentation review to ensure compliance.The ideal candidate should have a basic understanding of cell culture, fermentation, or purification unit operations, with preference given to those experienced in single-use platform technology. Strong written and verbal communication skills are essential. The role requires an energetic, motivated, and dynamic individual who is highly organized and capable of maintaining efficiency and a positive demeanor in a fast-paced, multitasking environment | 11/18/2025 |
| 191 | KBI Durham, NC Microbiology Associate I/II Bachelor’s/Master’s degree in Microbiology, Biology or related technological field of science Exp: 0 years |
Testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. | 11/18/2025 |
| 192 | KBI Durham, NC Research Associate I Bachelor’s degree in chemistry, biochemistry or related area Exp: 0+ years |
Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical Development (AD) Department. The individual in this position will be responsible for executing experimental protocols and performing data analysis in biopharmaceutical laboratories. | 11/18/2025 |
| 193 | KBI Durham, NC Research Associate II Master’s degree in chemistry, biochemistry or related area Exp: 0+ years |
Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical, Formulation and Stability (AFS) Department. This role is responsible for executing experimental protocols and performing elementary data analysis in the analytical laboratories. | 11/18/2025 |
| 194 | KBI Louisville, CO Research Associate I Bachelor’s degree in a scientific discipline Exp: 0-2 years |
Join an analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Rapid Analytics team. The individual in this position will support biophysical characterization studies of biopharmaceutical products through executing experimental protocols, performing data analysis, documenting work in technical reports, and presenting results to clients and management. Biophysical testing may include (but not limited to) SV-AUC, CD, DSC, FTIR, HPLC, UV-Vis. Required to work in teams to solve scientific problems, and to train and be trained by colleagues. | 11/18/2025 |
| 195 | KBI Boulder, CO Manufacturing Associate I Bachelor’s degree in a related scientific or engineering discipline Exp: 0-5 years |
Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels. | 11/18/2025 |
| 196 | KBI Durham, NC Microbiology Associate II Master’s degree in a scientific discipline Exp: 1 year |
The Microbiology Associate II will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. The position will be a first shift, 10-hour/shift position, located at the Hamlin Road facility. Responsibilities include laboratory support, program testing, reporting of results, execution of protocols. | 11/18/2025 |
| 197 | Kestra Kirkland, WA Systems Engineer MS degree of Engineering Exp: 1 years |
The Systems Engineer will interact with customers, customer advocates, stakeholders, human factors and a variety of engineering disciplines to understand intended product uses, product concepts and technology. They are directly responsible for the development, review and ongoing maintenance of high quality, well understood, broadly communicated system and software requirements and are expected to develop expertise in these same areas. | 11/18/2025 |
| 198 | Krystal Biotech Pittsburgh, PA Process Validation Associate Bachelors’ Degree in Chemical Engineering, Biomedical Engineering, or related Exp: 1+ years |
Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) or Engineer (3+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site. | 11/18/2025 |
| 199 | Krystal Biotech Pittsburgh, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 11/18/2025 |
| 200 | LabConnect Cleveland, OH Laboratory Technician - Sample Processing Services Bachelor’s degree, preferably in life sciences Exp: 1 year |
The laboratory technician is responsible for sample processing and aliquoting. Process samples, including nucleic acid extractions, PBMC/BMMC isolations, plasma separation, specimen aliquoting, and other methods as required. Ensure sample integrity to meet client expectations. | 11/18/2025 |
| 201 | Eurofins Tustin, CA Asbestos PLM Analyst Bachelor’s degree in microbiology, biology, geology or a closely related science Exp: 1+ years |
The Analyst primarily performs analysis of bulk samples using PLM for asbestos. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and enters laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 11/09/2025 |
| 202 | Eurofins Malvern, PA Characterization Scientist MS in Biochemistry, Chemistry, or related field Exp: 0-2 years |
Perform routine biochemical analyses for characterization of monoclonal antibodies in support of pharmaceutical development, including peptide mapping, A280, LCMS, size exclusion chromatography, fraction collection, or other routine methods. Sample preparation, distribution, and data collection, understanding of how to process data from chromatograms is a must. Reporting of data in accordance with requirements set forth by the department. Ensure maintenance of detailed documentation of assay development and qualification | 11/09/2025 |
| 203 | Eurofins Cedar Falls, IA Quality Assurance Assistant BS or BA in chemistry or related field Exp: 1-2 years |
The Quality Assurance Assistant assists the Quality Assurance (QA) Manager during audits and client visits. Helps maintain reference data in LIMS and performs spot audits internally at the request of the QA Manager. Performs customer service requests for Project Management staff, supplies SOP's, certification information, and method information. Works with the laboratory to maintain SOP's and other method performance documentation as directed by the QA Manager. | 11/09/2025 |
| 204 | Eurofins St. Charles, MO Associate Scientist I B.A. or B.S. Degree Exp: 6 months |
Eurofins Discovery provides lab research services for pharmaceutical and biotech organizations in a wide range of therapeutic areas to promote novel therapies for patients in need. This role will conduct industry leading cell-based and analytical assays in a laboratory setting with automated and classical methods. | 11/09/2025 |
| 205 | Eurofins Lancaster, PA Scientist - Data Review Bachelor’s degree in molecular/cellular biology or other related degree Exp: 1-2 years |
Ensure that the client receives high quality data and reports that adhere to client and good manufacturing process (GMP) requirements. Reviewing laboratory documentation for accuracy, consistency, and clarity. Gain a technical understanding of the techniques for the assays in which review is being performed. Begin to gain industry knowledge of the testing being completed within the department. Document work as required for GMP compliance | 11/09/2025 |
| 206 | Eurofins Cedar Falls, IA Quality Assurance Technician BS or BA in chemistry or related field Exp: 1-2 years |
The Quality Assurance Assistant assists the Quality Assurance (QA) Manager during audits and client visits. Helps maintain reference data in LIMS and performs spot audits internally at the request of the QA Manager. Performs customer service requests for Project Management staff, supplies SOP's, certification information, and method information. Works with the laboratory to maintain SOP's and other method performance documentation as directed by the QA Manager. | 11/09/2025 |
| 207 | Eurofins Rensselaer, NY QC Sampling Team Lead – Raw Materials Bachelor’s degree in Life Sciences or related field Exp: 1+ years |
As the QC Sampling Team Lead – Raw Materials, you will oversee a team responsible for sampling and inspecting raw materials used in biopharmaceutical manufacturing. You’ll ensure compliance with GMP standards, coordinate daily operations, and support team development while maintaining a strong presence in cleanroom environments. | 11/09/2025 |
| 208 | Evonik Birmingham, AL Microbiology Lab Technician Bachelor’s degree in microbiology, biological sciences, or related field Exp: 1 year |
This position is responsible for conducting routine microbiological testing, documentation, and data analysis, of utilities, raw materials, facilities and equipment. Additionally, the microbiology technician will be responsible for upkeep of the laboratory, laboratory supplies, and other various routine laboratory tasks. | 11/09/2025 |
| 209 | Evonik Lafayette, IN Facilities Plant Engineer Bachelor's degree in engineering (Civil, Structural, Architectural, Industrial, or Mechanical) Exp: 1-2 years |
The Plant Engineer oversees maintenance activities and small capital projects within assigned areas, providing independent engineering support to ensure safe, efficient, and compliant operations. The role defines, plans, and executes cost-effective projects in line with engineering standards, regulations, cGMP, and Evonik policies. The Plant Engineer drives continuous improvement to reduce costs and maintain high-quality, reliable operations, and may also lead medium-scale capital projects or support new product cost estimates. | 11/09/2025 |
| 210 | Evonik Birmingham, AL Validation and Qualification Specialist Bachelor’s degree preferably in Science or Engineering discipline Exp: 1-3 years |
Support existing qualification and Validation programs. Adhere to quality and regulatory compliance policies in support of GMP operations efforts. | 11/09/2025 |
| 211 | Evotec Redmond, WA Senior Associate Scientist, Purification Process Design BS or MS degree in Engineering, Biochemistry or related field Exp: 0-4 years |
We’re looking for a passionate and curious Senior Associate Scientist to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a Senior Associate Scientist at Just-Evotec, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team. | 11/09/2025 |
| 212 | Exact Sciences Phoenix, AZ Quality Control Associate I Bachelor’s degree in Clinical Laboratory Science or Medical Technology or in the chemical or biological sciences Exp: 1+ years |
The Clinical Laboratory Quality Control (QC) Associate (Tues - Sat and Sun - Thurs 10:00am - 6:30pm) performs and functions within the Technical Laboratory under the guided direction of the Supervisor, Clinical Laboratory Quality Control Lead, or designee. In this support position, the Clinical Laboratory QC Associate ensures daily QC operations are effective and efficient by coordinating with leadership to anticipate and resolve issues related to efficiencies in quality control, and laboratory processes. | 11/09/2025 |
| 213 | Fresenius Kabi Melrose Park, IL Validation Engineer Bachelor’s degree in a Science or Engineering field Exp: 1 year |
Responsible for providing technical support to operations in terms of equipment/system/process initial validation and equipment/system/process requalifications. Will participate in process and equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. The individual must become certified to enter Controlled Areas of the plant (class 100, 10,000 and 100,000). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 11/09/2025 |
| 214 | Fresenius Kabi Warrendale, PA Quality Engineer B.S. degree in Engineering (Mechanical, Electrical, Biomedical preferred) Exp: 0-3 years |
This position will analyze and execute processes to ensure product quality in the Production Unit (PU). This position will support core quality system processes to ensure compliance with applicable medical device regulations and standards (FDA, EU, Health Canada, ISO 13485) by providing operations assistance, tracking quality metrics, reviewing and approving quality system records, and analyzing data. Requires working in a cross-functional team environment. Applies engineering principles to resolve difficult problems. | 11/09/2025 |
| 215 | FUJIFILM Biotechnologies College Station, TX QA Analyst III Master’s Degree Exp: 1+ years |
The Quality Assurance (QA) Analyst III, under minimal direction, will be responsible for review and/or approval of basic and technical documentation, drafting and reviewing of internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing product release activities, identifying process and Quality System improvements, and acting as a QA liaison internally and externally. | 11/09/2025 |
| 216 | FUJIFILM Biotechnologies Mesa, AZ Development Lab Chemist Bachelor’s degree in chemistry or material science Exp: 1-5 years |
Responsibilities include supporting pilot line builds for formulated products, executing formulated products build plans, generating test data, assisting maintaining lab and pilot line equipment including 4-point probe, ellipsometer, FTIR, back up SEM/FIB and XRR operator, general lab assistance where needed. | 11/09/2025 |
| 217 | FUJIFILM Biotechnologies Mesa, AZ QC Chemist BA/BS in Chemistry or related degree such as Biochemistry, Biology, Physics or Mathematics. Exp: 0-1 years |
The QC Chemist serves as a Quality Control Specialist responsible for analyzing semiconductor materials in support of product qualification and to support all Quality Control laboratory processes. | 11/09/2025 |
| 218 | FUJIFILM Biotechnologies Research Triangle Park, NC Production Technician 3 Downstream Bachelor’s degree in life science, engineering, or relevant technical field Exp: No exp |
The Production Technician 3 executes manufacturing processing steps and associated activities while maintaining strict adherence to Current Good Manufacturing Practice (CGMP) quality and regulatory standards. Flexibility with working hours and shift rotation is essential to effectively support the 24/7 manufacturing facility. | 11/09/2025 |
| 219 | FUJIFILM Biotechnologies Holly Springs, NC Engineer / Scientist 2 Master’s degree Exp: No exp |
The Engineer/Scientist 2 will provide technology transfer support and technical oversight during manufacturing operations | 11/09/2025 |
| 220 | FUJIFILM Biotechnologies Holly Springs, NC Manufacturing Support Associate 1 BA/BS in life sciences Exp: No exp |
The Manufacturing Support Associate performs manufacturing support activities to ensure compliant and reliable production. This manufacturing facility is 24/7 operational and the role may require to be flexible with working hours. | 11/09/2025 |
| 221 | FUJIFILM Biotechnologies Research Triangle Park, NC Associate 1, Quality Control Microbiology Bachelor’s degree in Life Science or Biology Exp: No exp |
The Associate 1, Quality Control (QC) Microbiology is an entry level position responsible for performing routine microbiological testing of clean utility, environmental monitoring, and manufacturing batch samples. This role performs routine laboratory testing and support activities and participates in continuous improvement initiatives. | 11/09/2025 |
| 222 | Genentech South San Francisco, CA Scientist 2, Cell Culture, Protein Sciences Master’s degree in the Biological Sciences Exp: 1-3 years |
The departments of BioMolecular Research and Structural Biology, within the Protein Sciences Organization at Genentech are looking for a versatile, dynamic, and independent individual to contribute towards medium to large scale mammalian recombinant protein expression. In this collaborative role, the successful candidate will have the opportunity to work with other scientists and group leaders within and outside our department, driving projects autonomously to fulfill both straightforward and challenging protein production needs. | 11/09/2025 |
| 223 | Genentech Hillsboro, OR Automation Engineer BS degree in Engineering Exp: 0-2 years |
As a Frontline Automation Engineer, each day is a unique symphony of challenges and triumphs. Your role is pivotal in ensuring the timely delivery of life-saving medicines, making a tangible difference in the world. Every task you undertake, no matter how small, contributes to a larger purpose - the well-being of our patients. So, join our team in making a difference to Roche/Genentech and to our patients. You will be a member of the Frontline Automation Engineering Team which plays a key role in the support of our site’s make, assess, and release process. The individual selected into this role will provide frontline support and work collaboratively with maintenance, engineering, utilities, reliability teams, and end users to diagnose and troubleshoot equipment and processes. Additionally, you will work on project teams to deliver new capabilities and improve existing processes. The selected candidate will demonstrate a continuous improvement mindset and possess strong hands-on troubleshooting skills within a GMP environment. | 11/09/2025 |
| 224 | Genentech Hillsboro, OR Manufacturing Engineer B.S or higher in Mechanical Engineering, Electrical Engineering, Chemical Engineering, Biomedical Engineering, or related discipline Exp: 0-2 years |
As a Manufacturing Engineer at the Hillsboro Technical Operations Fill Finish facility, you will be responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as an equipment, process, or automation owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Manufacturing Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 11/09/2025 |
| 225 | Genezen Lexington, MA Analyst I, QC Raw Materials BS in Chemistry or other related science Exp: 1-3 years |
The Quality Control (QC) Raw Materials Analyst is responsible for ensuring the quality of raw materials are suitable for the intended use by the Manufacturing Department. These activities are performed in accordance with cGMP, USP, EP, and JP guidelines as well as company policies and procedures. The QC Raw Materials Analyst I will support the day-to-day operations which include sampling, internal and external testing, controlling and releasing raw materials, as well as support QMS (Deviations, CAPA, Lab Investigations (OOS, AR, OOT), Documentation (SOPs/Forms/Material Specification), laboratory operational processes and Training. Supports method validation/verification activities for onboarding new raw materials, as well as internal/external audits. | 11/09/2025 |
| 226 | Genezen Lexington, MA QC Lab Support (Contractor) BA or BS in Life Sciences Exp: 1-3 years |
The QC Lab Support Contractor plays a critical role in supporting day-to-day quality operations within the cGMP QC laboratories. This role is responsible for overseeing all aspects of GMP lab supply management, documentation and record keeping, lab equipment maintenance, reagent preparation and general lab support. In addition, individual will ensure compliance with documentation practices and contribute to maintaining an organized and efficient laboratory environment. This position is based at our state-of-the-art facility in Lexington, MA. | 11/09/2025 |
| 227 | Genezen Lexington, MA Process Engineer I, Manufacturing Sciences & Technology Bachelor's or Master's Degree in Engineering or other related scientific discipline. Exp: 0-3 years |
The Manufacturing Sciences & Technology (MSAT) group plays a critical role in successful manufacturing of clinical and commercial products. The person in this role assists the MSAT team in the transfer of technologies, process validation and cGMP manufacturing of Genezen’s gene therapy products. This individual will contribute as a core member of various cross-functional teams, and interacts extensively with other departments within Genezen including Process Development, Manufacturing, Engineering, Quality, and Regulatory Affair etc. | 11/09/2025 |
| 228 | Genezen Lexington, MA QC Technician - Microbiology (Contract) Bachelor's degree in Microbiology or other related science Exp: 0-2 years |
The QC Technician contract role will be responsible for routine and non-routine QC sampling and testing for the quality of products manufactured for our clients. QC is responsible for execution of the Environmental Monitoring (EM) program in place to monitor Genezen's controlled manufacturing environments (cleanrooms) as well as monitoring of utility systems including Water for Injection (WFI), Pure Steam, Purified Water, Compressed Air and Gas systems. These activities are all performed in accordance with cGMP guidelines and are supported by departmental and interdepartmental policies and standard operating procedures (SOPs). This position is based at Genezen’s state-of-the-art facility in Lexington, MA. This role supports daily operations as well as occasional weekend and holiday operations. | 11/09/2025 |
| 229 | GenScript Pennington, NJ Associate Scientist, Quality Control Bachelor’s degree in Molecular Biology, Biochemistry, Microbiology or related scientific field Exp: 1-2 years |
The position reports to the Sr. QC Manager, is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to lead and evolve this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients. | 11/09/2025 |
| 230 | GenScript Pennington, NJ (Sr). Scientist, Downstream Process Development Master’s in Chemical/Biochemical Engineering, Biological Sciences, or a related scientific discipline Exp: 1-3 years |
The position reports to the Associate Director, Downstream Viral Vector Process Development & MSAT Department. This role is ideally suited for a dynamic bench-focused individual to support/lead translation of research process to GMP-compliant manufacturing, and will develop, scale-up, and evaluate the technology transfer of viral vector processes. This is a great opportunity to join a fast-paced company, develop, and expand technical expertise to lead by example and potentially lead a small team in the near future. | 11/09/2025 |
| 231 | GenScript Pennington, NJ (Sr). Scientist, Upstream Process Development Master’s degree in Biology, Biochemistry, Chemical Engineering or equivalent Exp: 0-3 years |
The Scientist, Upstream Process Development & MSAT Department. reports to the Senior Manager, Upstream Viral Vector Process Development & MSAT Department. This role is ideally suited for a dynamic, bench-focused individual to support and lead the translation of research processes to GMP-compliant manufacturing. The successful candidate will develop, scale-up, and evaluate the technology transfer of viral vector processes in a fast-paced biotechnology environment. | 11/09/2025 |
| 232 | Getinge Wayne, NJ Engineer II, Mechanical MS in engineering discipline, mechanical preferred Exp: 1 year |
Effectively design, develop, and document medical devices and medical equipment that satisfy internal and external customer needs and business objectives. | 11/09/2025 |
| 233 | Gilead Foster City, CA Senior Research Associate, Formulation Process Development M.S in Pharmaceutical Science, Chemistry, Biochemistry, Chemical Engineering, or related scientific fields Exp: 0+ years |
Plan and successfully execute experiments and activities to support formulation and drug product process development. With general guidance, operate scientific equipment and tools such as HPLCs, UV-Vis, CE-SDS, and iCIEF to ensure applicable methods and techniques are followed. Clearly, timely, and accurately document data in appropriate repositories such as lab notebooks, reports, and protocols. Analyze, interpret, draw conclusions, and present or share data from executed experiments, including preparing appropriate documents such as reports and memos. Fully embrace a lean-agile mindset, a matrix working environment, and continuous improvement. Help support key project or department stakeholders as needed to ensure company objectives are met. Use established data, reports, and previous results to identify inappropriate variances and concerns, as well as identify and report inconsistent results to the manager or supervisor. Participate in group meetings and efforts by presenting data or preparing information for others to present. Support team initiatives to drive business process excellence, scientific innovation, and laboratory and work safety. | 11/09/2025 |
| 234 | Gilead Foster City, CA Sr Research Associate, Medicinal Chemistry Masters degree Exp: 0+ years |
As a Sr. Research Associate, you will participate a multi-disciplinary drug discovery team through the design and synthesis of new molecules. The successful candidate will have an excellent track record and a commitment to tackling drug discovery challenges through organic synthesis. | 11/09/2025 |
| 235 | Gilead Foster City, CA Research Associate, Medicinal Chemistry Bachelors degree Exp: 0+ years |
As a Research Associate, you will participate on a multi-disciplinary drug discovery team through the design and synthesis of new molecules. The successful candidate will have an excellent track record and a commitment to tackling drug discovery challenges through organic synthesis. | 11/09/2025 |
| 236 | Gilead La Verne, CA EH&S Specialist I MA/MS degree Exp: 0+ years |
An opportunity is available in the EH&S team at Gilead in La Verne, California. The successful candidate will be joining a highly motivated and cross functional team to help develop and elevate a proactive EH&S culture across our La Verne campus via administration of compliance related to our Sustainability and Injury and Illness prevention programs. You will use effective time management skills to work with limited supervision on routine projects to moderate complexity, including updating existing programs, protocols, and procedures. The Specialist will possess excellent communication and customer service skills and will be expected to maintain regular interaction with customer groups. | 11/09/2025 |
| 237 | Globus Medical Audubon, PA Project Engineer Bachelor's Degree in Mechanical Engineering, Bioengineering, Biomedical Engineering, or a similar field Exp: 0-3 years |
At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible. | 11/09/2025 |
| 238 | Globus Medical Audubon, PA Associate Quality Engineer Bachelor’s Degree required (science or engineering preferred) Exp: 0-2 years |
The Associate Quality Engineer will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. As a contributor to the quality engineering organization, this professional will be a self-motivated and characterized as an excellent problem solver. This person will play an integral role in maintaining | 11/09/2025 |
| 239 | Globus Medical San Diego, CA Electrical Engineer B.S. degree in Electrical Engineering Exp: 1-3 years |
Our rapidly growing medical robotics division is searching for an enthusiastic electrical engineer wanting to make a difference. Our skillful engineers develop medical robots by working with top surgeons and cross-functional engineering teams. The Electrical Engineer will be part of the electrical engineering team responsible for designing and implementing electronic circuits for intra-operative neuromonitoring used within our surgical navigation and robotic products. The position will be hands-on with the individual capable of creative, novel, and systematic product development with minimum supervision. | 11/09/2025 |
| 240 | Globus Medical Audubon, PA Regulatory Associate Bachelor’s degree in health or science-related field, or equivalent; Engineering degree is a plus Exp: 0-2 years |
The Regulatory Affairs Associate assists in drafting, submitting and gaining clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requiring working knowledge of products under review and of relevant regulations and guidance documents. This individual must be enthusiastic, positive, even-tempered and effective in building working relationships with internal teams while following FDA 21 CFR regulations. | 11/09/2025 |
| 241 | Cellares South San Francisco, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree or diploma in a scientific or related field Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 11/03/2025 |
| 242 | Cellares Bridgewater, NJ Cell Therapy Manufacturing Specialist Bachelor’s Degree or diploma in a scientific or related field Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Specialist to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 11/03/2025 |
| 243 | Cellares South San Francisco, CA Senior Systems Engineer Masters degree in Engineering, Physics or Biotech Automation Exp: 1 year |
We are seeking an innovative and highly motivated Senior Systems Engineer who will make significant contributions to the development of our advanced cell therapy manufacturing platform. The ideal candidate will have demonstrated experience in biomedical-related instruments and consumables development, integration, and verification activities. As a Senior Systems Engineer, you are expected to readily learn and adapt to Cell Shuttle technologies, take ownership of various tasks, and successfully drive them to completion. In your daily work, you will provide in-depth analysis for system characterization and troubleshooting, and help guide important decisions for continuous improvement projects. | 11/03/2025 |
| 244 | Cellipont Bioservices Woodlands, TX Manufacturing I Bachelors Degree in Life Sciences Exp: 0-1+ years |
Cellipont Bioservices is growing, and we are looking for a Manufacturing Associate I who believe in the potential bridging client's discoveries to patient cures and who want to challenge the status quo and take Cellipont and its clients to the next level. The Manufacturing Associate I is an entry level role and will be responsible for assisting in the planning and timely execution of manufacturing operations for a cGMP-compliant state-of-the-art cell processing/clinical manufacturing facility with emphasis on primary cell isolation and cell culture in an aseptic processing environment. The Manufacturing Associate I is responsible for following the standard practices outlined for the operation of the facility in accordance with the regulatory requirements for the manufacture of materials for our clinical studies, clinical trials and products. | 11/03/2025 |
| 245 | Cellipont Bioservices Woodlands, TX QA Technician I, Operations Bachelor's Degree Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician I, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician I, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician I, Operations is responsible for providing Quality Assurance support real-time for GMP Manufacturing of Cell Therapies. This individual will be responsible for providing QA on the Floor during manufacturing including observing critical processes, review executed GMP documentation, and supporting other QA functions as needed. | 11/03/2025 |
| 246 | Cellipont Bioservices Woodlands, TX QA Technician II, Operations Bachelor's Degree Exp: 1-2 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician II, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician II, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician II, Operations is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks. This individual will be responsible for providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. | 11/03/2025 |
| 247 | Cellipont Bioservices Woodlands, TX QC Analyst I, Analytical Bachelors Degree preferred in Life Sciences discipline Exp: -=1 years |
Cellipont Bioservices is growing, and we are looking for a QC Analyst I, Analytical who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QC Analyst I, Analytical will work in a fast-paced environment supporting the quality control department of a CDMO for manufacturing of cell therapies. The QC Analyst I, Analytical will be responsible for routine testing, assay transfer and assay validation, QC document preparation and revision (SOPs/Protocols/Reports), as well as support for laboratory setup and maintenance. The QC Analyst I, Analytical, will also be responsible for ensuring all activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will also require the individual to demonstrate a strong ability to work cross-functionally and possess strong leadership skills. | 11/03/2025 |
| 248 | Centrillion Palo Alto, CA Laboratory Technician B.A./B.S. in a molecular biology, genetics, or microbiology Exp: 6 months |
We are looking for a Laboratory Technician to join our R&D team in Palo Alto. The role is part of a small group that divides their focus between innovative new projects and product development. The ideal candidate will be extremely organized, familiar with basic laboratory techniques, and excited to learn and grow within the team. Technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. Candidates with knowledge and experience of PCR, library preparation, NGS sequencing or RNA seq will be given preference. | 11/03/2025 |
| 249 | Cepheid Lodi, CA Manufacturing Support Engineer Master’s degree of engineering related discipline Exp: 0-2 years |
The Manufacturing Support Engineer is responsible for supporting manufacturing operations with engineering expertise to ensure the successful transfer of new products from development to manufacturing, ensuring robust manufacturing processes at commercialization, conducting failure investigations of commercialized products, and supporting processes to ensure performance within expected parameters.. | 11/03/2025 |
| 250 | Champions Oncology Rockville, VD Research Associate I, Radiopharmacology BS or MS degree in radiochemistry, biochemistry, chemistry, chemical engineering, biomedical engineering, biology, or related sciences. Exp: 0-2 years |
Perform cross-functional laboratory assays with a focus on synthesis and purification of radiolabeled compounds and their characterization. Assist in the development and execution of novel assays including collecting and processing data. | 11/03/2025 |
| 251 | Charles River Reno, NV Quality Assurance Auditor I Bachelor’s degree (B.A./B.S.) Exp: 1-2 years |
The position is responsible for performing audits of basic records and reports and inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures. This individual will review protocols for compliance with all pertinent government and international GLP regulations for studies conducted at the Test Facility that are basic and routine in study design. The Quality Assurance Auditor will also prepare and review Quality Assurance files prior to Sponsor site visits; ensure that QA audit files are archived. | 11/03/2025 |
| 252 | Charles River Mattawan, MI Senior Associate Scientist, Project Scientist – Large Molecule Bioanalysis Master’s degree Exp: 1-2 years |
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays, such as enzyme-linked immunosorbent assay, to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic assays to measure drug and Immunogenicity assay to measure anti-drug antibodies and neutralizing antibodies. Other assay types also performed are branched DNA and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery, Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 11/03/2025 |
| 253 | Charles River Ashland, OH Research Analyst I, Formulations Bachelor’s degree (B.A./B.S.) in a relevant field Exp: No exp |
A Research Anaylst I – Formulations will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight. | 11/03/2025 |
| 254 | Charles River Spencerville, OH In Vivo Technician I Bachelor’s degree (B.A./B.S.) in a biological science Exp: No exp |
A Technician I is in training to perform and become proficient in on-boarding tasks, procedures, and cooperating in a team environment. The technician is learning basic tasks required to conduct a study, which may include collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. The technician is working under close supervision to gain proficiency | 11/03/2025 |
| 255 | Charles River Reno, NV Immunopathology Analyst I Bachelor’s degree (B.A. / B.S) in laboratory science or related discipline Exp: No exp |
Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. | 11/03/2025 |
| 256 | Charles River Ashland, OH Research Analyst I (Chemist) – Immunology Bachelor’s degree (B.A/B.S.) in scientific field Exp: 0-2 years |
Perform laboratory tasks by various basic methods. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. | 11/03/2025 |
| 257 | Charles River Mattawan, MI Associate Scientist – Discovery Immunoassays Master’s degree Exp: No exp |
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 11/03/2025 |
| 258 | Cipla Hauppauge, NY QA Validation - DPI Bachelor's degree in scientific discipline (e.g., biology, chemistry, pharmacy) or a related field Exp: 1-2 years |
Responsible for the coordination of supportive equipment and process validation activities such as testing, calibration, scale-up, engineering and validation studies, and assurance that the necessary project documentation is complete, accurate and in compliance with cGMP regulations. | 11/03/2025 |
| 259 | CPC Hauppauge, NY Chemist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Chemist is responsible for and has experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Microbiology, ICP, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 11/03/2025 |
| 260 | CooperSurgical Tucson, AZ Laboratory Services Quality Technician I Bachelor's degree in one of the biological, chemical, or physical sciences Exp: 1 year |
Quality Control Lab Technician I role at Cord Blood Registry (CBR) is responsible for analyzing and documenting test results from our cord blood and cord tissue processed samples, releasing raw materials, supporting the analytical and processing equipment maintenance program, conducting environmental monitoring, and providing a wide range of critical functions that support the cryogenic storage of our client's final product. This position is also responsible for providing our internal customers with technical expertise while maintaining the highest quality services possible. The Quality Control Lab Technician I directly supports manufacturing to ensure the Product Operations function is provided with adequate equipment and materials to support stem cell processing activities. At the Technician I level, the individual performs critical daily activities involving high complexity testing, equipment maintenance and troubleshooting, interfacing with service providers, reagent testing, executing quality control assays and environmental monitoring activities. The role is also involved with supporting and executing validations, verifications, and projects within the Quality Control department. | 11/03/2025 |
| 261 | Cardinal Health Mansfield, MA Regulatory Affairs Specialist Bachelors in related field Exp: 0-2 years |
Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function applies subject matter expertise to provide services in technical writing and regulatory submissions as well as clinical research and manufacturing process consulting. Regulatory Affairs plans, coordinates and implement regulatory strategies for products that require government approval. This job family proactively identifies regulatory requirements and risks for products and develops plans for product development programs and regulatory submissions. | 11/03/2025 |
| 262 | Cardinal Health Phoenix, AZ Development Engineer (Nuclear) Bachelor’s degree in related field (Electrical, Mechanical or Computer Science) Exp: 0-2 years |
As a Development Engineer, you will play a hands-on role supporting the design, testing, and improvement of systems that produce and distribute radiopharmaceuticals across the U.S. The Development Engineer is responsible for specific tasks and overall objectives to meet and exceed team and personal goals while managing multiple projects under general guidance. This role also conceptualizes project paths quickly and accurately, is a problem solver, and addresses challenges strategically and efficiently. | 11/03/2025 |
| 263 | Cardinal Health , Specialist, Quality Assurance Bachelor's degree Exp: 1-3 years |
The Specialist, Quality Assurance executes quality programs, policies, and procedures in a particular area of specialty (such as recalls and customer complaints) in order to minimize risks and drive supply chain integrity. With basic knowledge of quality assurance concepts, the Specialist creates reports on quality metrics and trends in support of resolutions to quality issues and the development of standard operating procedures. The Specialist frequently seeks guidance from more experienced Senior Specialists or Principal Specialists and assists on more complex projects to develop advanced knowledge and technical capabilities. | 11/03/2025 |
| 264 | Cresilon Brooklyn, NY Production Technician I Bachelor's or Master's Degree Exp: 0+ years |
The Production Technician I is responsible for the aseptic manufacturing of Cresilon’s products for the animal health industry. The Production Technician II will be trained in clean room operations, aseptic techniques, and must demonstrate the ability to successfully pass gowning qualifications. The position involves operating simple and complex processing equipment, routine sanitization of cleanroom facilities, and manual cleaning of equipment. The ideal candidate will have a proven track record of steady progress in a similar manufacturing environment and must possess a willingness to learn all equipment and jobs in the assigned manufacturing and sanitation of clean room facilities as required. Production Technicians are also responsible for the quality of products produced by ensuring compliance with local, State and Federal regulations, including current Good Manufacturing Practices (cGMP). | 11/03/2025 |
| 265 | Crown Bioscience Kannapolis, NC Research Associate I, Cancer Pharmacology (in vivo) Bachelor's degree in biology, pharmacology, physiology, animal science, or a related field Exp: 0-1 years |
The Research Associate (RA) at Crown Bioscience North Carolina will support the execution of in vivo research studies, contributing to the advancement of oncology and pharmacology research. The RA will work closely with scientists and senior research staff to carry out experiments, maintain animal models, collect and analyze data, and assist in the development of novel research techniques. This position plays a critical role in ensuring the quality and integrity of preclinical studies. | 11/03/2025 |
| 266 | Curia Albuquerque, NM Validation Specialist II Master’s Degree in Mechanical Engineering, or a related field Exp: 1 year |
Key responsibilities include conducting computer system validations to ensure adherence to GxP regulations, including 21 CFR Parts 210, 211, and 820, as well as compliance with Good Automated Manufacturing Practice (GAMP) standards. Ensures that change controls, records, and procedures align with current Good Manufacturing Practices (cGMP) and regulatory expectations. Coordinates validation activities with cross-functional teams to minimize impact on production schedules while ensuring timely execution. Responsible for authoring validation protocols, final reports, and technical summaries for the qualification and release of equipment, systems, instruments, components, and utilities. Support continuous improvement initiatives and provide mentorship to junior validation staff. | 11/03/2025 |
| 267 | Curia Rensselaer, NY Quality Assurance Specialist II Master’s Degree in Biomedical Engineering, or a related field Exp: 1 year |
Curia Global Inc. (Rensselaer, NY) seeks a Quality Assurance Specialist II for its Rensselaer, NY location. The position is responsible for assisting with validation activities throughout the plant and coordinate appropriate support. Assist in completing validation activities and provide technical assistance to Engineering Services, R&D, Production, Maintenance and QA/QC in Validation and Quality Assurance-related issues. | 11/03/2025 |
| 268 | Curia Hopkinton, MA Quality Control Lab Technician I Bachelor’s degree in Chemistry, Biology or related science Exp: 0-1 years |
The principal responsibility of Quality Control Lab Technician I is the analysis by multiple procedures of intermediates and target compounds. This role is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. A major component in the scientist's performance rating will be based on productivity. In general, the Quality Control Lab Technician I provides technical, organizational and compliance support for 170+ ongoing stability studies. The incumbent is encouraged to display a degree of professionalism reflected in part by increasing the scientist's knowledge of theory and practice through reading scientific journals and texts at times beyond the "normal" working hours. | 11/03/2025 |
| 269 | Curia Rensselaer, NY validation Specialist II Bachelor’s degree in Chemistry or related field Exp: 0-3 years |
The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications. | 11/03/2025 |
| 270 | Cytiva Pensacola, FL Electrical Project Engineer Bachelor’s degree in engineering (electrical preferred) Exp: 1+ years |
The Electrical Project Engineer is responsible for the Design, Implementation, and Qualification of membrane manufacturing equipment (electrical portions). This includes component and vendor selection as well as contractor supervision. | 11/03/2025 |
| 271 | Dexcom San Diego, CA Systems Engineer 2 - Mobile and Wearable Software Master’s degree Exp: 0-2 years |
Join a passionate team of engineers who are truly making a difference in the lives of people living with diabetes. As the Systems Engineer 2 – Mobile and Wearable Software, you'll be central to ensuring our Dexcom mobile and wearable applications meet the highest standards of safety, usability, and performance. Join our collaborative Systems Engineering team and contribute to technology that empowers users to manage their health with confidence through intuitive, cutting-edge software. If you're driven, thrive in a fast-paced environment, and passionate about turning complex needs into robust software requirements, this is the team for you! | 11/03/2025 |
| 272 | Dexcom San Diego, CA Process Development Engineer 2 Master’s degree Exp: 0-2 years |
The Sensor Process Development team provides global ownership and supports sensor development and manufacturing. As part of the Operations organization, the team ensures process modernization and improvements for sensor safety, sensor accuracy, and sensor reliability resulting in positive outcomes for our users every day. The team has expertise across many subject areas and experience levels, leading to a collaborative environment with innovative solutions. This role will support technical projects related to sensor process development and provide expertise in design and understanding process impact on sensor performance. | 11/03/2025 |
| 273 | Diacarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science Exp: 0-1 years |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 11/03/2025 |
| 274 | Diacarta Pleasanton, CA Research Associate BS or MS degree in molecular biology or a related field Exp: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 11/03/2025 |
| 275 | Diacarta Pleasanton, CA Manufacture Technician BS degree in Molecular Biology, Cell Biology, Biotechnology or related field Exp: 1 year |
Purchase raw materials from a vendor. Receive incoming materials and perform inspection and inventory recording. Production of DiaCarta IVD products to meet sales demands. Labeling of raw materials and finished goods. Perform calibration or preventative maintenance of the instrument. Participate in process improvement projects. Compliance with corporate quality systems. Other on-the-job assignments indicated by management | 11/03/2025 |
| 276 | DM Clinical Research Houston, TX PBMC Lab Technician Bachelor’s degree Exp: 1-2 years |
A PBMC Laboratory Technician will be responsible for conducting special laboratory procedures for clinical trials performing high complexity laboratory techniques including, but not limited to routine isolation of peripheral blood mononuclear cells (PBMC), or other laboratory procedures, etc., ensuring safety measures are followed by facilitating laboratory operations. | 11/03/2025 |
| 277 | Endo Hobart, NY Process Engineer BS degree in Industrial, Manufacturing, Chemical Engineering or Packaging Engineering/Technology or related field Exp: 1-3 years |
Improves safety, quality, and productivity of a fast-paced solid dose pharmaceutical operation. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies. Serve as the main point of contact for manufacturing and/or packaging processes in their area regarding safety, quality, and continuous improvement activities. | 11/03/2025 |
| 278 | Enovis Austin, TX Quality Engineer Bachelor’s degree in Engineering, Life Sciences, or a related field Exp: 0-2 years |
We are seeking a detail-oriented and proactive Quality Specialist to join our Quality Department in Austin, TX. This fast-paced role is ideal for someone passionate about quality systems, metrics, and continuous improvement. You will play a key role in supporting and managing quality processes including Field Actions, CAPAs, SCARs, and NCMRs, ensuring full compliance with internal procedures and regulatory standards. Reporting directly to the QMS Manager, this position is responsible for maintaining and reporting critical quality metrics that reflect the overall health of plant operations and production/quality controls. These metrics are regularly shared with senior leadership and cross-functional teams to drive performance, accountability, and compliance across the organization. | 11/03/2025 |
| 279 | EnPlusOne Watertown, MA Research Associate - Synthesis Bachelor’s degree in Molecular Biology, Biochemistry or Chemistry Exp: 1 year |
Your primary role as a Research Associate on the Synthesis team at EnPlusOne is to support the enzymatic RNA synthesis platform. You will assist staff scientists in RNA synthesis, reaction screening, data analysis, buffer preparation, QAQC, and inventory. You will work on multiple internal projects and external collaborations. You will be expected to keep a well-documented lab notebook, stay highly organized, use good communication, and collaborate well with our awesome team. Successful candidates are self-starters who are endlessly curious, excited by research, and flexible in a fast-paced, constantly evolving field. | 11/03/2025 |
| 280 | Enveda Boulder, CO NMR Scientist M.S. Exp: 1-3 years |
At Enveda, every role drives impact. As a NMR Scientist, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in NMR spectroscopy, instrument maintenance and structure elucidation will be critical in accelerating our mission to advance our pipeline of novel small-molecule therapeutics because every breakthrough starts with bold questions and brave actions. | 11/03/2025 |
| 281 | BioMarin Novato, CA Research Associate, Process Analytics Bachelors degree in biological sciences Exp: 1-2 years |
The Analytical Sciences department at BioMarin Pharmaceutical Inc. is seeking a skilled Analytical Biochemist and/or Biologist at the Research Associate level to join a team focused on supporting gene therapy & enzyme replacement therapy. The successful candidate will be a self-motivated, independent and critical thinker who has experience of working in a multi-disciplinary and fast-paced environment, and solid communication skills. The candidate will execute a wide variety of analytical methods and assays for the characterization of therapeutic candidates in development with a particular focus on testing to support clinical and commercial process development teams. | 10/27/2025 |
| 282 | Biomerics Salt Lake City, UT Staff Design Transfer Engineer Master Degree in Engineering Exp: 1+ years |
The Staff Design Transfer Engineer will be responsible for designing and developing complex medical devices from concept to production, ensuring they exceed customer expectations. You will be expected to work directly with customers to understand product needs, define process specifications, develop manufacturing processes, and build and test devices to those specifications. This role will focus mainly on the processes and fixtures required to consistently manufacture endoscopes. This role collaborates early in the concept phase to guide the team toward manufacturability and repeatability of a design. This role is expected to bring relevant experience to the team and improve the design or process to exceed our customer expectations. | 10/27/2025 |
| 283 | Biomerics Salt Lake City, UT Design Transfer Engineer Master Degree in Engineering Exp: 1+ years |
The Design Transfer Engineer will be responsible for designing and developing complex medical devices from concept to production, ensuring they exceed customer expectations. You will be expected to work directly with customers to understand product needs, define process specifications, develop manufacturing processes, and build and test devices to those specifications. This role will focus mainly on the processes and fixtures required to consistently manufacture endoscopes. This role collaborates early in the concept phase to guide the team toward manufacturability and repeatability of a design. This role is expected to bring relevant experience to the team and improve the design or process to exceed our customer expectations. | 10/27/2025 |
| 284 | bioMérieux Lombard, IL QC Analyst Bachelors degree in biology or related field Exp: 0-3 years |
We are seeking a detail-oriented and motivated Quality Control (QC) Analyst. This role will support the quality of our products. This position must prioritize lots to ensure schedule and goals are met. Responsible for ensuring performance testing meets data specifications. Perform all duties using safety conscious practices. This is an excellent opportunity for individuals passionate about quality and continuous improvement within a manufacturing industry. | 10/27/2025 |
| 285 | bioMérieux Salt Lake City, UT BioReagents Formulator Bachelor’s degree with an emphasis on a biological science Exp: 1+ years |
The Bioreagents Formulator position plays a vital role in the manufacturing and quality process by preparing high-precision reagents and buffers that power our diagnostic testing platforms. This individual will be responsible for the formulation of PCR master mixes, process controls, and large-scale buffers that are later integrated into test kits by our production teams. Accuracy, consistency, and adherence to quality standards are essential as the materials produced directly support our customers’ ability to deliver reliable results to patients worldwide. | 10/27/2025 |
| 286 | Bio-Rad Irvine, CA Production Chemist I Bachelor’s degree in a life science or related field Exp: 0-3 years |
Formulates products and intermediates utilizing biologicals and chemicals of varying properties and characteristics in order to meet specifications | 10/27/2025 |
| 287 | Bio-Rad Fort Worth, TX Manufacturing Engineering Tech I Bachelor’s degree in Engineering, Biotechnology, or a related scientific/technical discipline Exp: 1-5 years |
The Manufacturing Engineering Technician’s day begins with reviewing maintenance and calibration schedules, coordinating with vendors, and ensuring production equipment is operational and compliant. Throughout the day, they troubleshoot issues, perform IOPQ testing, support R&D and manufacturing engineers with experiments or prototypes, and coordinate facility-related tasks. They also update procedures, assist with QN/NC/CAPA documentation, research equipment or components, and provide hands-on support for manufacturing activities as needed. | 10/27/2025 |
| 288 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline Exp: 1-6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 10/27/2025 |
| 289 | Bio-Techne Minneapolis, MN Advanced Research Associate Master’s degree in biological sciences Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. | 10/27/2025 |
| 290 | Bio-Techne Minneapolis, MN Research Associate - QC Stem Cell B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Performing routine quality control testing of stem cell products using protocol-defined assays to demonstrate their activity. The assays include culturing and handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation and workflow is required. Other duties include instrumentation maintenance, reagent preparation and routine lab support for QC antibody testing using western blot, simple wes and immunohistochemistry. | 10/27/2025 |
| 291 | Bio-Techne Minneapolis, MN Research Associate - Conjugation Bachelor’s degree in chemistry, biological sciences, or equivalent Exp: 0-2 years |
As a Research Associate in the Conjugation lab, you will be responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, you may help prepare and test other chemistry related reagents for manufacturing and QC teams. | 10/27/2025 |
| 292 | Bio-Techne Minneapolis, MN Research Associate - QC Bioassay Bachelor’s degree in the biological sciences or equivalent Exp: 0-2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 10/27/2025 |
| 293 | Bio-Techne Minneapolis, MN Research Associate - Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday to Saturday shift. | 10/27/2025 |
| 294 | BioSpectra Bangor, PA Qualification Specialist Bachelor’s degree in Science, Engineering or other related discipline Exp: 1 year |
This position is responsible for ensuring that equipment, systems, and processes are qualified and validated in accordance with regulatory requirements and BioSpectra’s standards. This includes developing, executing, and reporting on equipment, instrumentation, and control system qualifications and re-qualifications | 10/27/2025 |
| 295 | Blueprint Medicines Cambridge, MA Associate Scientist Biology Master’s degree in Bioengineering, Biomedical Engineering, or a closely related biological or life sciences field Exp: 1 year |
Research, identify, and validate novel oncology targets and small molecule drug discovery, utilizing knowledge of bioengineering to develop and conduct cellular assays to support Blueprint Medicine’s novel drug discovery efforts. | 10/27/2025 |
| 296 | Boston Scientific Maple Grove, MN Quality Engineer II Master’s degree in engineering Exp: 1+ years |
Quality Engineer II will be a key member of the Nitinol Shape Memory team supporting the self-expanding component product lines. This role will partner with representatives from the Manufacturing Engineering and Production functions. The person in this role will take the lead in addressing quality issues in a dynamic production environment. The ideal candidate will be comfortable interfacing with downstream internal customers and providing quality leadership to a production team running across 4 shifts. | 10/27/2025 |
| 297 | Bristol Myers Squibb Bothell, WA Specialist - MSAT Cell Therapy Engineering Services, Process Support BS and/or MS degree in Science or Chem/Bio Engineering Exp: 1+ years |
The primary focus of the Specialist - MSAT Cell Therapy Engineering Services, Process Support is to provide product and process support to Cell Therapy Manufacturing Operations at Bristol Myers Squibb’s GMP facility in Bothell, WA. | 10/27/2025 |
| 298 | Bristol Myers Squibb Bothell, WA Associate I, Manufacturing Bachelor's degree in related field Exp: 0-1 years |
Our Associates perform a crucial role in driving our novel cell therapy programs by supporting routine manufacturing operations. We are searching for innovative, intellectually curious individuals with a general understanding of Good Manufacturing Practices (GMPs) to support routine manufacturing operations for Cell Therapy. Successful candidates must be goal-oriented and flexible, with the ability to work effectively and efficiently on a team while demonstrating safety, quality, and GMP compliance at all times. | 10/27/2025 |
| 299 | Bristol Myers Squibb Bothell, WA Associate II, Manufacturing Labels & Issuance Bachelor's degree in related field Exp: 1+ years |
This role is part of the Bothell Manufacturing Logistics & Services team and will focus supporting cGMP Manufacturing Operations for the BMS Bothell site, including the coordination, issuance, reconciliation, and management of production labels and records. Functional responsibilities include all batch label and documentation control activities for Cell Therapy Operations (CTO), including performing and maintaining a GMP compliant clinical and commercial batch documentation and label issuance and control process. | 10/27/2025 |
| 300 | Bristol Myers Squibb New Brunswick, NJ Kilo-Lab Associate Scientist MS in Chemistry or Chemical Engineering Exp: 0-2 years |
The Associate Scientist is required to possess mechanical aptitude and the ability to perform tasks involving manual work. While supporting personnel are available to assist with material handling and equipment setup, the Kilo Lab Associate Scientist is responsible for overseeing and conducting batch activities. Typically, the Kilo Lab handles processes ranging from laboratory-scale up to 200L vessels. This facility serves as a testing ground for new manufacturing technologies, such as flow chemistry and emerging methodologies, in which the scientists frequently participate. | 10/27/2025 |
| 301 | Bristol Myers Squibb Devens, MA Sr. Specialist, QC Analytical Bachelor’s degree in science, engineering, biochemistry or related discipline Exp: 1-3 years |
The Senior Specialist, QC Analytical, Cell Therapy is responsible for supporting Quality Control bioanalytical testing for method validation, critical reagent qualification, in-process, release, and stability testing of clinical and commercial cell therapy drug product. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. Additionally, the QC Senior Specialist will assist with training and assay transfer. The QC Senior Specialist role is stationed in Devens, MA and reports to the Manager, QC Analytical for the Devens CTF. | 10/27/2025 |
| 302 | Bristol Myers Squibb Devens, MA Specialist, Associate Process Engineer, Cell Therapy BSc and/or MSc degree in Science or Chem/Bio Engineering Exp: 0-3 years |
The Specialist, Associate Process Engineer, Cell Therapy provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process. The Associate Process Engineer works closely with the Manufacturing and Quality teams to determine immediate corrective actions for deviations, identifies root cause, and implements long-term preventive actions. Other responsibilities include participation in process tech transfer, supports incoming process changes by communicating the changes to applicable departments, and participates in process improvement projects at the site. The process engineer works to identify and drive continuous improvements to the manufacturing process. | 10/27/2025 |
| 303 | Bristol Myers Squibb Devens, MA Associate, QC Microbiology, Cell Therapy Bachelor's degree preferred in science Exp: 0-2+ years |
Bristol Myers Squibb is seeking a Associate, QC Microbiology, Cell Therapy to join our QC Microbiology team at the Cell Therapy Facility (CTF) in Devens, MA. Responsible for supporting QC testing for in-process, final product, stability samples and for supporting environmental and facility monitoring. May assist with documentation, deviations, investigations, and continuous improvement efforts. | 10/27/2025 |
| 304 | Bruker Kirkland, WA Staff Electromechanical Technician BS degree in electronic engineering Exp: 0-3 years |
The Bruker AXS-EM division is looking for an electromechanical technician to do board level debugging of PCBs on our electron microscope products. Bruker AXS-EM electronics span a wide range from high-speed digital cameras and scanning systems to ultra stable precision current supplies to 200kV high voltage supplies with tens of millivolt stability. The successful candidate will be able to handle multiple projects simultaneously, making sure that things come together in a timely manner. Help others as needed. Responsibilities will shift and grow based on ability and interests. Light travel to Asia and Europe is a possibility but not a requirement. | 10/27/2025 |
| 305 | Cambrex High Point, NC Scientist 1 - QC M.S. in Chemistry or related field Exp: 0 years |
The Scientist 1 - Quality Control role perform routine analytical testing on raw materials, intermediate, and final products as well as in-process testing; perform data entry; draft deviations, and participate in OOS investigations for their testing with some supervision. Ensure compliance with applicable Company SOPs and regulatory guidance’s. | 10/27/2025 |
| 306 | Cambrex Waltham, MA Associate Chemical Engineer Bachelor’s or Master’s degree in Chemistry, Chemical Engineering, or a related discipline Exp: 1-3 years |
Snapdragon Chemistry is currently seeking exceptional candidates to join the Engineering and Manufacturing team in Waltham, MA. A successful candidate will be joining a group of innovative and entrepreneurial engineers and scientists, with broad deliverables including the development of reactor systems and purifications for continuous flow processes, delivery of high quality, complex chemical matter to our clients, and transferring process technology to clients at their facility. The ideal candidate will have a degree in chemical engineering with experience and a passion for developing new process technology. The candidate should enjoy building equipment and carrying out process development and manufacturing activities in a laboratory or kilo-laboratory environment. The candidate should be well versed in process development and scale-up activities, including common reaction, separation and purification techniques, such as working with 10-100L batch reactors, liquid-liquid extractions, vacuum distillation, filtration, and crystallization. Experience with the development of reactions in flow is preferred but not required. Candidates must possess strong written and oral communication skills. | 10/27/2025 |
| 307 | Candel Needham, MA Contract Research Associate – Virology MS in Virology, Biotechnology, or related field Exp: 1-3 years |
We are seeking a highly motivated and collaborative Research Associate with a strong foundation in virology to support the development of next-generation HSV-1 viral immunotherapy candidates. This individual will contribute to the enLIGHTEN™ Discovery Platform through hands-on experimental work, including viral vector testing, mammalian cell culture, and virology-specific assays. The ideal candidate will bring a passion for innovation and a desire to work in a fast-paced, cross-functional research environment. | 10/27/2025 |
| 308 | Capricor Therapeutics San Diego, CA Manufacturing Associate Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field Exp: 1-3 years |
As a Manufacturing Associate I/II, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success. | 10/27/2025 |
| 309 | Capricor Therapeutics San Diego, CA MSAT Training Specialist Bachelor’s degree in life sciences or equivalent Exp: 1-3 years |
As an MSAT Training Specialist at Capricor, you will play a pivotal role in ensuring operational excellence and GMP compliance across our cell therapy manufacturing processes. This position focuses on designing and delivering robust training programs, mentoring manufacturing personnel, and maintaining documentation that supports regulatory readiness and high-quality production. Ideal candidates thrive in a dynamic biotech environment, combining technical expertise with a commitment to continuous improvement and team development. | 10/27/2025 |
| 310 | Caris Phoenix, AZ Molecular Technologist, Solid Tumor Bachelor’s or Master's degree in scientific field Exp: 0-1 years |
The Molecular Technologist – Solid Tumor is responsible for performing various high complexity molecular techniques that include but are not limited to nucleic acid extractions and next generation sequencing (NGS). This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 10/27/2025 |
| 311 | Carlsmed Carlsbad, CA Clinical Engineer BS or MS degree in a technical field such as Engineering, Life Sciences, Computer Sciences, Mathematics or related medical/scientific field Exp: Entry Level |
The Clinical Engineer is a skilled data-savvy contributor who receives and organizes inbound clinical data in various formats from multiple research sites engaged in Carlsmed-sponsored studies. The role involves receiving, vetting, and forwarding medical images to measurement services and parsing large data sets into subsets for analysis. | 10/27/2025 |
| 312 | Castle Biosciences Pittsburgh, PA Lab, Molecular Technologist Bachelor of Science Degree in Chemistry, Biology, Clinical Laboratory Science, or Medical Technology Exp: 1-2 years |
A typical day for the molecular technologist includes RNA extraction utilizing a mixture of manual and automated methods, RT-PCR performed via manual pipetting, and sample loading on array chips for final result determination. The technologist would be working with equipment setups for all processes, as well as reagent preparations, specimen management, and assisting with inventory and quality management tasks as needed. This role will spend the most time on specimen management and preparation, in-house control creation and reagent Q.C. testing, and quality control checks and documentation associated with high complexity clinical laboratory testing. | 10/27/2025 |
| 313 | Catalent Kansas City, MO BioAnalytics Laboratory Technician Bachelor’s degree in scientific field Exp: No exp |
Catalent Pharma Solutions in Kansas City, MO is hiring a BioAnalytics Laboratory Technician. The BioAnalytics Laboratory Technician supports the BioAnalytics team by performing basic analytical and Good Manufacturing Practices (GMP) testing, maintaining laboratory operations and equipment, and ensuring compliance with safety and quality standards. This role is ideal for individuals beginning their careers in life sciences or pharmaceutical industry. Training will be provided, and the technician will work under close supervision while developing technical skills and regulatory knowledge. | 10/27/2025 |
| 314 | Catalent Kansas City, MO Controlled Substance Specialist II Bachelor's degree Exp: 1+ years |
Catalent Pharma Solutions in Kansas City, MO is hiring Controlled Substance Specialist II. The Controlled Substance Specialist II will support the state of DEA regulatory compliance of controlled substances at the KCM site through the following: oversee the inventory and other aspects regarding the use and storage of controlled substances in pharmaceutical dosage forms in development, laboratory, manufacturing, and packaging environments. Support all necessary regulations with DEA 21 CFR 1300 to end, Bureau of Narcotics and Dangerous Drugs and state licensure, state reporting and maintaining NABP Drug Distributor Accreditation. | 10/27/2025 |
| 315 | Catalent Madison, WI Associate II - Quality Assurance Bachelor's Degree in STEM discipline Exp: 1 year |
The Quality Assurance Operations group has oversight of the manufacturing areas, including process technology transfer, master batch record review and approval, on-the-floor support, product disposition, and shipping. | 10/27/2025 |
| 316 | Catalent Greendale, IN Engineer, Manufacturing, Sciences, and Technology M.S. in Chemical Engineering, Chemistry, Biology, Life Sciences or a related field Exp: 1+ years |
The Engineer, Manufacturing Sciences and Technology (MS&T) is responsible for supporting GMP manufacturing operations as a project leader to commercialize new products and optimize commercial manufacturing processes. The Engineer, MS&T assists in translating client and process development information into cGMP process implementation. | 10/27/2025 |
| 317 | Catalent Winchester, KY Quality Assurance Associate Bachelor's Degree Exp: 1+ years |
The Quality Assurance Associate is responsible for the Quality support functions associated with the manufacturing of solid oral dosage products. The QA Associate is responsible for the oversight of the manufacturing operations (as dictated by cGMP, CFR, and Catalent SOP) through document review/approval, real time monitoring/approval of manufacturing activities and testing/approval of in-process and finished product samples. | 10/27/2025 |
| 318 | Catalent Greenville, NC Project Engineer I Master's degree in Engineering Exp: 1 year |
The Project Engineer I will assure projects are executed in accordance with current site methodologies, policies, industry best practices, and cGMP requirements. The role will leverage the knowledge of GMPs and manufacturing processes to ensure that projects are executed with minimal disruption to operational schedules and must provide construction management oversight to ensure that projects are completed safely, efficiently, and in accordance with all applicable codes and requirements. | 10/27/2025 |
| 319 | Catalent St. Petersburg, FL Associate Scientist II, QC BS or BA in related sciences Exp: No exp |
The Associate Scientist II, Quality Control will independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. In addition, this role will Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines, communicate results in written and oral presentations, help in writing Procedures, Specifications and Test Methods. The Associate Scientist II, Quality Control will keep abreast of literature in field; help train colleagues; contribute to continuous improvement within the group, comply with FDA, EPA and OSHA regulations, performing all work in a safe manner and maintain proper records in accordance with all SOP's and policies. | 10/27/2025 |
| 320 | Celerion Lincoln, NE Scientist/ Associate Scientist of Laboratory Automation Bachelor's degree Exp: 1 year |
Celerion is hiring a Scientist/ Associate Scientist of Laboratory Automation to join our Lincoln, NE Bioanalytical team. This role will work onsite daily with our Hamilton, Tecan and Sciclone instruments. In this role, you will perform research and/or development in collaboration with scientific teams and automated systems based on new and existing methodologies. This hands-on role focuses on programming and operating laboratory automation systems with the objective of becoming the subject matter expert for all laboratory automation technologies within our organization. | 10/27/2025 |
| 321 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone with expertise in classifying diseases/conditions by medical specialty to do drug pipeline confirmation tasks. Contract work on a task basis. Must be able to accept payment by PayPal or Venmo. Also must be able to function in the world without using ChatGPT, because if we thought AI could do the task well, you would not be reading this job posting. Please send a message through the contact form if interested. | 09/07/2025 |
| 322 | Bio-Techne Minneapolis, MN Research Associate, Analytical QC B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, endotoxin assay, TOC, conductivity and other testing as assigned. The position requires routine documentation, analysis and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity and team building across the QC Department or the entire company. Perform additional duties as assigned. | 10/21/2025 |
| 323 | Bio-Techne San Marcos, CA Chemistry Associate Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 years |
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 10/21/2025 |
| 324 | Bio-Techne Minneapolis, MN Advanced Research Associate Master’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday to Saturday shift. | 10/21/2025 |
| 325 | Bio-Techne Devens, MA Manufacturing Technician Bachelor’s degree Exp: 0+ years |
Understand and follow appropriate standard operating procedures and work instructions. Regulatory awareness of chemical handling and hazards. Labeling. Safety procedures. Department specific SOP’s. Proper use and basic equipment maintenance. Follow priorities from supervision. Document results, process, and refer to past batch records. Complete all compliance trainings as assigned. Participate in continuous process improvement efforts. Works independently with minimal supervision on routine tasks. Ability to support and help others in the team. Knowledge of work performed by the department and learning how to perform multiple functions within the department. Flexibility to work on multiple tasks with increased effectiveness. Primary operator of manufacturing equipment, including equipment changeovers. Understand and repair minor mechanical issues with manufacturing equipment. Assist in training of new and temporary hires in the Manufacturing Department. Assist with equipment pack line or manual pack line operations. Identify process improvements and flag areas for improvement. Meet quality and productivity expectations. Manages time well and will put in extended time as needed. Willingness to accept changes in work from day-to-day within reasonable and expected boundaries. Perform other duties as assigned within and outside the department. | 10/21/2025 |
| 326 | Bio-Techne Minneapolis, MN Scientific Support Associate Bachelor’s degree in Biological Sciences, Biochemistry, or equivalent Exp: 0-2 years |
Answers and documents incoming customer inquiries by phone, email, and chat. Meets with customers via video conference – Teams, Zoom, Webex, etc., as needed. Addresses inquiries on instrument and software operation, product selection, techniques, procedures, and performs simple troubleshooting. Initiates complaints and works with the appropriate team(s) to resolve. Documents communications and resolutions in Salesforce (CRM, Customer Relationship Management Database). Provides adequate information to the Scientific Support teams to problem solve or to assist with resolution of issue. Communicates with Scientific Support Team, Customer Service, Field Service and Applications, and Sales teams regarding ongoing cases and issues. Documents information and recurring technical issues to support product quality programs and product development. Assists Scientific Support in department functions/projects including but not limited to the maintenance of technical resources, training materials, and FAQs. Supports Marketing and internal teams by providing Voice of Customer. Initiates replacement orders if required by complaint. Is aware of Field Notifications and required actions. Keeps up to date on current technology and use of product lines by attending seminars, reading current scientific literature, and using products in lab. Keeps up to date with training and reading Standard Operating Procedures (SOPs). Follows company policies and practices as outlined in Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene, and Exposure Control manuals in accordance with the job. Performs additional duties as assigned. | 10/21/2025 |
| 327 | Bio-Techne Newark, CA Quality Control Associate B.S./B.A. in molecular biology, biochemistry, cell biology or related field Exp: 1+ years |
The Quality Control Associate supports all product release testing activities from raw material to finished good products and product stability. This role involves in process testing of incoming raw materials, analytical testing, bulk functional testing, and kit lot release testing in accordance with ISO 13485 GMP requirements. | 10/21/2025 |
| 328 | Alphatec Spine Carlsbad, CA Design Engineer Bachelor’s degree in mechanical or biomedical engineering Exp: 1-4 years |
Under routine supervision, primarily responsible for the enhancement of existing products on our sustaining team. Involved in creating concepts and modeling and drafting designs utilizing 3D CAD software. Other responsibilities include drafting of design history file documents, development of test plans to assess designs, and assisting in the development processes for Manufacturing, Quality Control, Regulatory and Planning for their particular project. | 10/21/2025 |
| 329 | August Bioservices Nashville, TN Manufacturing Technician II/III Bachelor's degree in biological, chemical sciences, or engineering Exp: 1+ years |
August Bioservices is seeking to hire experienced manufacturing technicians to support our growing formulations and filling teams. Headquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! | 10/21/2025 |
| 330 | Avance Biosciences Houston, TX Laboratory Associate II Bachelor’s degree in biological sciences Exp: 1 year |
Carry out Molecular Biology, Microbiology, and Protein experiments following established SOPs and/or the guidance of laboratory management. Perform DNA/RNA extraction, quantification, and gel QC. Perform PCR setup for qualitative and quantitative analysis. Report experimental results to project managers in a timely manner. Follow established quality management policies and GLP and GMP practices. | 10/21/2025 |
| 331 | Avantor Paris, KY Quality Technician Bachelor’s degree in a science discipline Exp: 1+ years |
Conducting routine and non-routine chemistry and microbiological analysis of raw materials, in-process formulations, and final products to established specifications. Working independently with limited direct supervision. Following through on multiple projects and being a goal-oriented achiever. Demonstrating business-level interpersonal and organizational skills. Wearing a half-face respirator if required. Utilizing and operating laboratory equipment and instruments according to laboratory work instructions or procedures such as pH, conductivity, UV, KF, FTIR, and titrations. Performing chemical tests requiring manual dexterity and sensory discrimination as these tests involve measuring, weighing, and other precise tasks. Completing Resource Conservation and Recovery Act (RCRA) training. Understanding and following written and verbal instructions. Understanding and following Quality Control test methods or compendia methods (USP, EP, BP, JP, or ACS) and EXCIPACT standards. Supporting department management and performing defined tasks to comply with and maintain the site’s ISO 9000/1400 certification and all regulatory requirements. Initiating operation shutdowns and notifying management if questions regarding compliance or issues requiring additional attention arise. Regulatory requirements include, but are not limited to, cGMPs, EPA, OSHA, DEA, DOT, and other applicable local, governmental, and company guidelines. Calculating and generating data for compliance to specifications and reporting results. Performing technical review of lab data forms such as water, environmental monitoring, and direct measure analysis. Calibrating and maintaining lab equipment. Entering results and raw data for tested materials or products in LIMS (Laboratory Information Management System) as needed. Conducting investigative analysis to support investigations, complaints, or instrument troubleshooting. Performing environmental monitoring duties, which require gowning into cleanrooms and collecting air and surface samples while in cleanroom environments. Reviewing for discrepancies in data, manufacturing COAs, COCs, and performing data verification in accordance with company procedures. Applying appropriate disposition labels to materials (accepted, rejected, etc.). Handling hazardous materials using all appropriate or mandatory safety PPE and safety equipment. Completing documentation in a legible manner and reviewing for accuracy. Performing other duties as assigned. | 10/21/2025 |
| 332 | Avantor Waltham, MA Sr. Lab Technician-Media/Buffer Bachelor’s degree in a scientific discipline Exp: 1-2 years |
In this role, you will report to the Onsite Supervisor and will work closely with the Avantor’s Advanced Laboratory Services professionals to serve our customers by performing customized, mission-based lab work and research protocols that help return time back to science. | 10/21/2025 |
| 333 | Avantor Waltham, MA Sr. Lab Technician-Solvent Management Bachelor’s degree in a scientific discipline Exp: 1-2 years |
In this role, you will report to the Onsite Supervisor and will work closely with the Avantor’s Advanced Laboratory Services professionals to serve our customers by performing customized, mission-based lab work and research protocols that help return time back to science. | 10/21/2025 |
| 334 | Avid Bioservices Tustin, CA Research Associate, Process Development Downstream B.S. degree in a Biological Science Exp: 1-2 years |
The Research Associate, Process Development Downstream will provide laboratory support for Process Development by assisting in the downstream process and/or method development. The Research Associate may be assigned various tasks within the department and outside the department as needed. | 10/21/2025 |
| 335 | Avid Bioservices Tustin, CA Research Associate, Process Development Upstream B.S. degree in a Biological Science Exp: 1-2 years |
The Research Associate in Process Development - Upstream will develop and optimize scalable cell culture processes and contribute to transferring the process to Avid Manufacturing. In addition, the Research Associate will maintain production equipment and will research and implement new methods and technologies to enhance process operations. | 10/21/2025 |
| 336 | Avive Brisbane, CA Quality Engineer, Failure Analysis BS in Engineering (preferably Electrical or Biomedical) Exp: 1-4 ears |
The Quality Engineer, Failure Analysis will be responsible for investigating complaints, internal non-conformances, and collaborating with various teams to ensure thorough investigations of product hardware and software issues. This role will be responsible for generating failure investigations reports, metrics and data analysis. | 10/21/2025 |
| 337 | Boston Analytical Salem, NH Chemist II Bachelor’s degree in Chemistry or a related discipline Exp: 1+ years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 10/21/2025 |
| 338 | Boston Analytical Salem, NH Microbiologist I, QC BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/21/2025 |
| 339 | Boston Analytical Salem, NH Microbiologist I, VD BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist conducts validation and feasibility testing for quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/21/2025 |
| 340 | Boston Analytical Salem, NH Microbiologist I, MB BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/21/2025 |
| 341 | Boston Analytical Morrisville, NC Microbiologist I, Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 10/21/2025 |
| 342 | Boston Analytical Morrisville, NC Sample Control Technician Bachelor’s degree in a scientific discipline Exp: 0-2 years |
The Sample Control Technician is responsible for ensuring that all samples are entered into the Laboratory Information Management System (LIMS) and made available to the lab staff in a timely manner. In addition, this position will manage lab inventory, including but not limited to tracking, shipping, and receiving of materials. As needed, this individual will coordinate and assist the metrology department in calibrations and equipment. This position reports to the Associate Director, Microbiology. | 10/21/2025 |
| 343 | Bachem Vista, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 10/21/2025 |
| 344 | Baxter Marion, NC Quality Lab Associate I - Bioburden B.S. degree in Microbiology, Biology, or related science Exp: 1 year |
Conduct microbiological analysis on raw materials, solution, and components following approved Standard Operating Procedures in an accurate and timely manner. | 10/21/2025 |
| 345 | Baxter Round Lake, IL Quality Lab Associate I Bachelors degree in Chemistry or Science related degree Exp: 6+ months |
The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. | 10/21/2025 |
| 346 | Baxter Marion, NC Quality Lab Associate III - Validation Analytics Master’s in Natural Sciences Exp: 1-3 years |
Responsible for performance and efficiency of Analytical Validation and Qualification activities. Lead and/or coordinate activities in support of analytical validation operations to ensure safe operations, effective planning, and regulatory compliance in the performance of method, process, cleaning, and stability validations for various chemical products while maintaining high standards for quality and responsiveness to production requirements. | 10/21/2025 |
| 347 | Baxter Round Lake, IL Sr Electrical Engineer Masters in Electrical or Electronics or related Engineering Exp: As the Sr. Electrical Engineer, you will develop creative solutions to challenging problems associated with the design of our new and existing infusio |
This person will be involved with coordinating and managing the Quality Assurance activities in all areas of the production/manufacturing processes. This will consist of ensuring quality standards are met in the manufacturing of products. This person must be able to effectively communicate vital information to various personnel throughout the organization. | 10/21/2025 |
| 348 | Baxter Irvine, CA Sr QA Inspector, QM Lab Bachelors Degree in science-related field Exp: 0-2 years |
Responsible for endorsing process and product quality, efficacy, and safety through the routine assessment of plant operations and finished products. Responsible for ensuring adherence to the regulatory and procedural requirements that govern those operations and products. | 10/21/2025 |
| 349 | Baxter Marion, NC Quality Lab Associate I - Environmental Monitoring B.S. degree in Microbiology, Biology, or related science Exp: 1 year |
Supports the environmental monitoring program by performing testing such as surface testing, viable air monitoring, and air total particle counts. Responsible for conducting routine risk assessments and HEPA filter inspections in clean-rooms. | 10/21/2025 |
| 350 | Boston Scientific Maple Grove, MN R&D Engineer III Master's degree in Mechanical Engineering, Biomedical Engineering, or related field Exp: 1+ years |
We are looking for a dynamic R&D Engineer III to support the growing TheraSphere Y90 franchise. In this role, you will make important contributions to support new product development and exploratory initiatives on the TheraSphere Y90 R&D team. This role offers a unique opportunity to work on a global team developing innovative technologies in the field of interventional oncology! | 10/21/2025 |
| 351 | Boston Scientific Maple Grove, MN Manufacturing Technician II Bachelor’s Degree in Engineering, Technology, or related field Exp: 1 year |
As a Manufacturing Technician II, you are responsible for performing functions associated with all manufacturing operations in daily support of products, processes, materials, and equipment in order to achieve production goals (i.e., quality, delivery, cost, productivity, and safety. Daily tasks include responding to equipment downtimes issues on the production floor, performing routine preventative maintenance on production equipment, and supporting Manufacturing Engineers (ME) in value improvement projects. Most of your time is spent on the production floor, working on equipment, and engaging with our Medical Device Specialists (i.e. MDS operators). With General Supervision, you will work on 1st shift as part of a technician team in the Nitinol Shape Memory (NSM) business unit. NSM 1st shift runs Monday-Friday from 5:30am to 1:30pm. | 10/21/2025 |
| 352 | Boston Scientific Maple Grove, MN Electrical Engineer I Bachelor’s degree in electrical or similar Engineering Exp: 0-2 years |
We have an exciting opportunity for an Electrical Engineer I, focusing on New Product Development (NPD), Sustaining, and Compliance on the Coronary Therapies team within the Interventional Cardiology (IC) division here at Boston Scientific. This role will utilize a variety of new and proven technologies to deliver life-changing medical devices to patients and clinicians in support of BSC’s mission. | 10/21/2025 |
| 353 | Boston Scientific Maple Grove, MN Quality Engineer II Master’s degree in engineering Exp: 1+ years |
Quality Engineer II will be a key member of the Nitinol Shape Memory team supporting the self-expanding component product lines. This role will partner with representatives from the Manufacturing Engineering and Production functions. The person in this role will take the lead in addressing quality issues in a dynamic production environment. The ideal candidate will be comfortable interfacing with downstream internal customers and providing quality leadership to a production team running across 4 shifts. | 10/21/2025 |
| 354 | Beckman Coulter Diagnostics Chaska, MN Quality Assurance Engineer I Bachelor’s degree in engineering (i.e. Mechanical or Electrical) Exp: 0-2+ years |
The Quality Assurance Engineer I is responsible for Quality Assurance support for Instrument Manufacturing. This position reports to the Quality Manager and is part of the Instrument Mfg. Quality Assurance team located in Chaska, MN and will be an on-site role. | 10/21/2025 |
| 355 | Beckman Coulter Diagnostics Miami, FL Manufacturing/Process Engineering II Master's degree in Mechanical, Electrical, or Industrial Engineering Exp: 0-2 years |
The Manufacturing/Process Engineering II for Beckman Coulter Diagnostics is responsible to ensure quality meets desired standards, compliance with safety protocols and regulatory standards, provides training to personnel on new processes, equipment and procedures and track and meet key performance indicators. This position reports to the Senior Manager of Technical Operations and is part of the Manufacturing Technical Operations team located in Miami, FL, and is an onsite role. | 10/21/2025 |
| 356 | BD Covington, GA Regulatory Affairs Specialist I BS in a scientific field Exp: 1+ years |
Provide regulatory support through the product life cycle on product project teams (e.g., developing regulatory strategies, timeline development, change control and preparing submission related documents). Prepare and audit 510(k)s, IDEs, PMA and/or international submissions as required. Provide technical collaborate with FDA and international reviewers and respond to questions. Provide timely review and approval of product labeling and marketing claims for regulatory compliance. Provide support required for CE marking activities, including preparation and maintenance of product technical files and clinical evaluations | 10/21/2025 |
| 357 | BD Salt Lake City, UT Engineer II - Research and Development Bachelor's degree (preferred) in STEM or related field Exp: 0-5+ years |
BD (Becton Dickinson and Company), a leading global medical technology company, is seeking a Research and Development Engineer II to work on the sustainability and development of medical devices for BD’s healthcare products. They assume the technical role of projects and champion technical and architectural excellence. The candidate should be passionate about solutions to clinician and patient unmet needs, and enjoy the details involved with the long-term outlook of technological solutions to clinical needs. The position is an exciting opportunity to make a meaningful, positive impact on patients throughout world by leveraging cutting edge technologies. | 10/21/2025 |
| 358 | BD San Diego, CA Biochemist II - Bead Manufacturing Master’s degree in a science-related field Exp: 1-3 years |
The Biochemist II, Beads Manufacturing must have working knowledge of fluorescence microparticle manufacturing. This role will conduct data analysis to solve complex problems with various factors. The Biochemist II is responsible for improving process efficiencies and product quality. This position will also support and participate in continuous improvement projects as identified by the leadership team and assigned by the Manager. | 10/21/2025 |
| 359 | BioAgilytix Durham, NC Analyst II (Cell-based GMP) Master's degree in molecular biology, biochemistry, immunology, biotechnology, or related field Exp: 1 year |
We are looking for candidates who have scientific lab experience in a deadline-driven setting. The best candidates are people who have hands-on experience in a lab environment (academic or professional) and are curious about applying different scientific methods, equipment and extraction processes. If you are a person who is energized by project variety and learning from top scientists in our industry, then you’ll be right at home here at BioAgilytix. | 10/21/2025 |
| 360 | bioMérieux Salt Lake City, UT BioReagents Formulator Bachelor’s degree with an emphasis on a biological science Exp: 1+ years |
The Bioreagents Formulator position plays a vital role in the manufacturing and quality process by preparing high-precision reagents and buffers that power our diagnostic testing platforms. This individual will be responsible for the formulation of PCR master mixes, process controls, and large-scale buffers that are later integrated into test kits by our production teams. Accuracy, consistency, and adherence to quality standards are essential as the materials produced directly support our customers’ ability to deliver reliable results to patients worldwide. | 10/21/2025 |
| 361 | BioMarin Novato, CA Manufacturing Associate Bachelor's degree in a science-related area or engineering Exp: 1-2 years |
Operating large-scale bioprocess equipment for Cell Culture, Purification, or Buffer and Media processing; performing all aspects of processing with a broad understanding of science, compliance, and technical aspects; displaying competency with process equipment and automated control systems; performing cleaning and sterilization of parts and equipment used in the manufacturing process; and having knowledge of biotech manufacturing processes and equipment, including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation, and/or buffer and media operations. The candidate should have the ability to understand, apply, and evaluate basic chemistry, biology, and scientific principles as appropriate for the position. Proficiency with compliance, adherence to standard operating procedures, batch records, good documentation practices, and data capturing is also essential. | 10/21/2025 |
| 362 | Alcami Wilmington, NC Scientist II - Chemistry Masters degree in Chemistry, Biochemistry, or related field Exp: 0+ years |
The Scientist II (Chemistry) is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing in addition to other key methodologies such as KF and titration. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) and may also assist with method development / method validation projects. | 10/15/2025 |
| 363 | Alcami Wilmington, NC Scientist II - QC Chemistry Masters degree in Chemistry, Biochemistry, or related field Exp: 0+ years |
The Scientist II - QC Chemistry is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing in addition to other key methodologies such as KF and titration. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) and may also assist with method development / method validation projects. | 10/15/2025 |
| 364 | Alcon Houston, TX Building Automation Engineer Master’s Degree Exp: 0+ years |
As a Building Automation Engineer, you will be trusted with the design, implementation, and optimization of advanced building automation systems (BAS) across our manufacturing campus. You will work with Johnson Controls (JCI) platforms to integrate HVAC, fire, security, and energy systems, ensuring operational efficiency, regulatory compliance, and environmental control at our Manufacturing Facility in Houston, TX. | 10/15/2025 |
| 365 | Alcon Fort Worth, TX Sr. Optical Engineer - Integrated Optical System Master’s Degree Exp: 0+ years |
The Sr. Optical Engineer is primarily responsible for supporting optical engineering efforts through testing, data analysis, and research to enhance optical system design. You will be expected to collaborate with teams to validate optical models, refine testing procedures, and contribute to the development of high-performance optical solutions. The Sr. Optical Engineer within the Integrated Optical System function will support metrology system development and qualification. | 10/15/2025 |
| 366 | Alcon Fort Worth, TX Sr. Associate, Mechanical Design Engineering Master’s Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Sr. Associate, Mechanical Design Engineering supporting Alcon's Engineering function, you will be trusted to work on developing innovative intraocular devices and improving quality, processes, products, packaging and materials across our business to help deliver brilliant outcomes. | 10/15/2025 |
| 367 | Alcon Johns Creek, GA Sr. Associate, Facilities Engineer Master’s Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Sr. Associate, Facilities Engineer supporting the MTO Chemical Team in Johns Creek, GA. | 10/15/2025 |
| 368 | Alcon Johns Creek, GA Sr. Associate, Controls Engineer Master’s Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Sr. Associate Controls Engineer supporting the U.S. MTO Team in Johns Creek, GA. | 10/15/2025 |
| 369 | Alcon Johns Creek, GA Sr. Associate, Automation and Control Engineering Master’s Degree Exp: 0+ years |
As a Sr. Associate, Automation and Control Engineering, supporting our supporting our Engineering Manufacturing Systems team, you will be trusted to design, implement, install, analyze and/or optimize manufacturing processes, procedures, equipment, and programming. The ideal candidate will also have expertise in PLC and automation controls, ensuring seamless integration and functionality of mechatronic systems to best support our 24/7 operation at Johns Creek, GA. | 10/15/2025 |
| 370 | Alcon Fort Worth, TX Senior Engineer II Master’s Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Senior Engineer, II supporting mechanical design projects by tackling complex mechanical design tasks, refining components, conducting performance analyses, and troubleshooting. You will be expected to build effective and meaningful relationships with engineering teams and apply advanced modeling and simulation techniques. | 10/15/2025 |
| 371 | Aldevron Madison, WI Scientist I- Downstream PD Master’s in biology, biotechnology, molecular biology, biochemistry, chemistry, or a closely related field Exp: No exp |
The Scientist I position is part of the Downstream Process Development (DSPD) team in the Protein Business Unit of Aldevron. This is an on-site position at the facility located in Madison, WI. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Technical Operations team (encompassing DSPD and other teams) and your responsibilities will revolve around developing processes to purify recombinant proteins from microbial host expression systems. | 10/15/2025 |
| 372 | Alkermes Wilmington, OH Temp-QC Analyst-Microbiology Bachelor's in science, preferably in Biology / Microbiology / Biotechnology or Biochemistry Exp: 1+ years |
QC Analyst I must have broad knowledge of microbiology techniques within the laboratory required for the routine support of the microbiology laboratory operations. In this role the Analyst will be a fully functional member of the team responsible for testing and data entry for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment | 10/15/2025 |
| 373 | Alkermes Wilmington, OH Process Engineer I/II/Lead-OSD BS degree in Engineering or technical discipline Exp: 0-2 years |
This position will support and assist in manufacturing pharmaceutical products for commercial and clinical supplies. Key duties include scale-up and transfer of oral solid dosage formulations/processes to the production facility, designing and recommending equipment purchases, and writing and executing equipment specification and commissioning protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process/equipment improvements (utilizing Change Control systems) to reduce waste and increase process reliability. Assure the resolution of deviations, corrective actions, action items from Change Control systems, and any audit non-compliance items. Perform process and equipment evaluation (FMEA, etc) to identify risks and weaknesses in new and current processes. Develop and implement SOPs in support of new and upgraded processes. Champion projects as they move into and through the manufacturing areas. Provide regular updates to leadership on project status and issues. | 10/15/2025 |
| 374 | Altasciences Harleysville, PA Senior Formulation Scientist MS in Pharmaceutical Sciences or in a related discipline Exp: 1-3 years |
Senior Formulation Scientist will be responsible for the formulation development for small and complex molecules, including controlled-release, liposomal, and spray-dried dispersions (SDD). This role requires deep expertise in oral and advanced formulation technologies. The scientist will evaluate innovative drug delivery approaches and support development from preclinical through late stage. This position collaborates closely with manufacturing and analytical teams to ensure successful technology transfer for GMP manufacturing. | 10/15/2025 |
| 375 | Altasciences Columbia, MO Necropsy Technician Bachelor of Science (B.S.) Exp: 6 months-1 year |
To provide high quality and timely processing of pathological specimens through gross examinations, necropsies, tissue trimming and tissue processing as specified in company protocols and SOPs. | 10/15/2025 |
| 376 | Altasciences Columbia, MO Scientist, LCMS Bachelor’s degree in Immunology/ Biology/ Chemistry or equivalent discipline Exp: 6 months |
You will assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. You will also support and perform data collection activities including primarily focused on mass-spectrometry. | 10/15/2025 |
| 377 | Alturas Analytics Moscow, ID Assistant Scientist Bachelor’s degree in a physical, biological or chemistry science Exp: 1-3 years |
We’re looking for a detail-oriented, team-focused Assistant Scientist to join our dynamic bioanalytical laboratory. We are dedicated to providing ample opportunities for growth and promotion within our team. You’ll work closely with experienced Senior Scientists, gaining hands-on expertise in a supportive and engaging environment. | 10/15/2025 |
| 378 | Amgen New Albany, OH Senior Associate IQA Bachelor’s Exp: 6 months |
In this vital role you will be responsible for sampling, inspection and dispositioning all raw materials received at the facility under general supervision. A key aspect of this role is to apply critical thinking skills to ensure quality and compliance to GMP regulations for all area operations and associated processes. Duties include batch record review, SOP creation & review, documentation, review & approval of minor deviations and CAPA records and batch disposition of raw materials. | 10/15/2025 |
| 379 | Amgen Thousand Oaks, CA Associate Scientist Master’s degree Exp: 1 year |
Let’s do this. Let’s change the world. We are seeking an Associate Scientist with expertise in high-throughput mass spectrometry-based proteomics. In this vital role, you will be part of the Discovery Proteomics team based in Thousand Oaks, CA. The discovery proteomics team delivers key insights into target and drug discovery by supporting pipeline programs and advancing platform technologies through mass spectrometry. In this role, you will drive pipeline advancement and screening platform by performing automated sample preparation and analysis for a range of high-throughput proteomic assays. This position requires hands-on experience with sample preparation for mass spectrometry analysis using liquid handlers, as well as proven expertise in operating high-throughput mass spectrometers. Your contributions will play an important role in high-throughout drug screening and pipeline support. | 10/15/2025 |
| 380 | Amgen West Greenwich, RI Senior Associate Quality Control Bachelor’s Exp: 6 months |
Let’s do this. Let’s change the world. In this vital role you will provide testing support for the QC Night Shift“Team C”(Saturday - Tuesday from 9:45pm – 8:15am)at Amgen Rhode Island. | 10/15/2025 |
| 381 | Amneal Piscataway, NJ Associate Maintenance Engineer Bachelors Degree (BA/BS) Engineering, Pharmaceutics, Industrial Pharmacy, or related field Exp: 1+ years |
The Associate Maintenance Engineer supports the upkeep, optimization, and reliability of pharmaceutical manufacturing equipment and utilities. The successful candidate will assist in the maintenance, troubleshooting, continuous improvement and plays a crucial part in ensuring smooth production of oral solid dosage forms and transdermal systems, including birth control patches. This role is critical to ensuring equipment reliability, operational efficiency, and compliance with GMP and regulatory standards. | 10/15/2025 |
| 382 | Amneal Piscataway, NJ ssociate Automation Engineer Master Degree (MS/MA) Electrical Engineer, Electrical & Electronics Engineer Exp: 1 year |
The Automation Engineer's primary role is to work under supervision and coordinating installation, troubleshooting and assist in maintaining automated processes and facility related equipment. | 10/15/2025 |
| 383 | Applied Medical Rancho Santa Margarita, CA Machine Design Engineer, Automation Bachelor's degree in Mechanical Engineering or in a related field Exp: 1 year |
Are you a visionary Design Engineer? Join Applied Medical and be at the forefront of revolutionizing medical device manufacturing. As part of our Automation team, you will be at our global U.S. headquarters, pioneering cutting-edge machines, collaborating across departments, and leading the way in cost reduction, optimizing manufacturing processes. As a Design Engineer, you will play a vital role in supporting the development of automated machines or automated processes for our in-house medical device manufacturing. It's your chance to make an enduring impact on the future of healthcare. | 10/15/2025 |
| 384 | Applied Medical Rancho Santa Margarita, CA Document Control Engineer I Bachelor's degree in Engineering, Physical or Biological Sciences, another technical discipline, or equivalent Exp: 1 year |
As a Document Control Engineer I, you will be responsible for working within the framework of a team and performing the following activities: Understand and comply with Applied Medical's Quality Systems (QS), safety rules, and company policies. Coordinate and respond to questions and act as a liaison to internal and external customers/ Review, monitor, and approve programs and documentation, as assigned, to ensure compliance with relevant standards, regulations, and guidance documents. Work with Systems, Applications & Products in Data. Processing (SAP) system to understand and maintain material masters, bill of materials (BOMs), and routers. Maintain and improve internal document procedures. Identify and implement systems to improve the overall efficiency of processes within Document Control/ Perform additional duties and responsibilities, as needed | 10/15/2025 |
| 385 | Applied Medical Lake Forest, CA Manufacturing Design Engineer Bachelor’s degree in Mechanical Engineering or related technical field Exp: 1+ years |
Join Applied Medical and be at the forefront of precision medical device manufacturing. As a Manufacturing Design Engineer, you’ll merge engineering creativity with hands-on design expertise, developing equipment and automation solutions to support sub-assembly workflows product integration. In this dynamic, production-facing role, you’ll collaborate with PPD teams, machinists, and cross-functional engineers—applying your CAD skills and mechanical intuition to design tooling, prototype components, and support the build and validation of custom equipment that enhances throughput, quality, and manufacturability across the floor. | 10/15/2025 |
| 386 | Applied Medical Rancho Santa Margarita, CA Complaint Evaluation Engineer Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering or a similar engineering discipline Exp: 1 year |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. | 10/15/2025 |
| 387 | AMT’ Cleveland, OH Quality Manager Bachelor's Degree in Engineering Exp: 1-5 years |
This person will be involved with coordinating and managing the Quality Assurance activities in all areas of the production/manufacturing processes. This will consist of ensuring quality standards are met in the manufacturing of products. This person must be able to effectively communicate vital information to various personnel throughout the organization. | 10/15/2025 |
| 388 | AMT’ Cleveland, OH Quality Assurance Supervisor Bachelor's Degree in Engineering Exp: 1-5 years |
This person will be involved with coordinating and managing the Quality Assurance activities in all areas of the production/manufacturing processes. This will consist of ensuring quality standards are met in the manufacturing of products. This person must be able to effectively communicate vital information to various personnel throughout the organization. | 10/15/2025 |
| 389 | ARL Bio Pharma Oklahoma City, OK Chemist I - Analytical Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 10/15/2025 |
| 390 | ARL Bio Pharma Oklahoma City, OK Microbiologist I Bachelor’s degree in Microbiology or related science Exp: 0-2 years |
Under the supervision of the laboratory supervisor the Microbiologist I provides a high level of quality pharmaceutical microbiology testing as well as effective customer service to ARL Bio Pharma clients. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. | 10/15/2025 |
| 391 | ARL Bio Pharma Oklahoma City, OK Chemist I - R&D Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 10/15/2025 |
| 392 | AstraZeneca Gaithersburg, MD Associate Scientist, Analytical Sciences, GMP Bachelor’s or master’s degree in chemistry, biochemistry or related field Exp: 0-5 years |
Are you ready to dive into the world of Analytical Sciences within GMP regulations? Join our dynamic team responsible for supporting clinical stage biopharmaceutical products. We manage lot release and stability programs, reference standards, critical reagents, and more. Collaborate with experts across multiple analytical disciplines such as chromatography, electrophoresis, immunoassay, bioassay, and device functionality methods. Work closely with Analytical Sciences development personnel, Clinical Supply Chain, CMC, and Quality Assurance throughout all stages of clinical development. | 10/15/2025 |
| 393 | AstraZeneca Frederick, MD Production Technician I -Nights BS/BA degree in STEM field Exp: 0-1 years |
In this role, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also train with a qualified Technician on activities related to operating process equipment with the requirement of qualification. Additionally, you will follow and execute cGMP documentation, utilize Manufacturing Execution systems (MES), contribute to problem-solving activities for non-routine activities on the production floor, and participate in continuous improvement activities for Manufacturing. Adherence to AstraZeneca values and behaviors is expected. | 10/15/2025 |
| 394 | AstraZeneca Gaithersburg, MD Scientist, Oncology TCR-T Cell Therapy Master's Degree in Immunology, Cancer Biology, Cell Biology, or relevant scientific field Exp: 1 year |
We are seeking a highly motivated and independent Scientist to join our rapidly growing Cell Therapy Team. In this role, you will contribute to advancing innovative Cell Therapy products by designing and conducting laboratory experiments, developing methodology, and generating and interpreting scientific data in a highly collaborative environment.Expertise inin vitro and in vivo studies and T cell biology is critical for this role. To be successful in this role, you must be well-organized and keep an excellent written record of your work. You will be based in Gaithersburg, MD and report to the Associate Director, TCR-T Cell Therapy. | 10/15/2025 |
| 395 | AstraZeneca Gaithersburg, MD Associate Specialist, Clinical Biologics Bachelor’s degree in a science related field Exp: 0-4 years |
As an Associate Specialist in the clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role, you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic, and gaining knowledge and experience in cell culture, purification and critical support activities. Under the supervision of highly trained personnel, you will gain the process knowledge and skill sets to perform large scale clinical development activities through hands-on training. You will join a collaborative and driven team in a world class biopharmaceutical company that is driving disruptive innovation in the industry. | 10/15/2025 |
| 396 | Bio-Techne Devens, MA Manufacturing Technician Bachelor’s degree Exp: 0+ years |
Understand and follow appropriate standard operating procedures and work instructions. Regulatory awareness of chemical handling and hazards. Labeling. Safety procedures. Department specific SOP’s. Proper use and basic equipment maintenance. Follow priorities from supervision. Document results, process, and refer to past batch records. Complete all compliance trainings as assigned. Participate in continuous process improvement efforts. Works independently with minimal supervision on routine tasks. Ability to support and help others in the team. Knowledge of work performed by the department and learning how to perform multiple functions within the department. Flexibility to work on multiple tasks with increased effectiveness. Primary operator of manufacturing equipment, including equipment changeovers. Understand and repair minor mechanical issues with manufacturing equipment. Assist in training of new and temporary hires in the Manufacturing Department. Assist with equipment pack line or manual pack line operations. Identify process improvements and flag areas for improvement. Meet quality and productivity expectations. Manages time well and will put in extended time as needed. Willingness to accept changes in work from day-to-day within reasonable and expected boundaries. Perform other duties as assigned within and outside the department. | 10/15/2025 |
| 397 | Bio-Techne Minneapolis, MN Scientific Support Associate Bachelor’s degree in Biological Sciences, Biochemistry or equivalent Exp: 0-2 years |
The responsibilities of this position, Scientific Support Associate (SSA), are to respond to incoming technical inquiries from the Bio-Techne commercial team and Bio-Techne's North American customers, providing first-tier technical and sales assistance for R&D Systems, Tocris, and Novus products. Completes all customer requests including e-mail responses and simple quotes. Maintains technical resources. Backs up Customer Service and Sales departments as necessary. Continues training to stay up to date on technical information for old and new products. Performs additional duties as assigned. | 10/15/2025 |
| 398 | Bio-Techne Minneapolis, MN Research Associate - QC Stem Cell B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Performing routine quality control testing of stem cell products using protocol-defined assays to demonstrate their activity. The assays include culturing and handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation and workflow is required. Other duties include instrumentation maintenance, reagent preparation and routine lab support for QC antibody testing using western blot, simple wes and immunohistochemistry. | 10/15/2025 |
| 399 | Bio-Techne Minneapolis, MN Research Associate - Conjugation Bachelor’s degree in chemistry, biological sciences, or equivalent Exp: 0-2 years |
As a Research Associate in the Conjugation lab, you will be responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, you may help prepare and test other chemistry related reagents for manufacturing and QC teams. | 10/15/2025 |
| 400 | Bio-Techne Minneapolis, MN Research Associate - QC Bioassay Bachelor’s degree in the biological sciences or equivalent Exp: 0-2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 10/15/2025 |
| 401 | Bio-Techne Minneapolis, MN Research Associate - Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday to Saturday shift. | 10/15/2025 |
| 402 | Vaxcyte San Carlos, CA Associate Scientist II, Drug Product Analytics MSc in Chemistry, Biophysics or Biochemistry Exp: 1 year |
Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, including immunoassays, chromatography, spectrophotometric techniques, light scattering, and particle sizing. Experience in analyzing vaccine and adjuvant-containing formulations is a plus. In addition, Vaxcyte is looking for an experienced and flexible individual who would be comfortable working on multiple projects at once, with fluid prioritization to enable aggressive timelines. This position is for a lab-based scientific role and requires excellent scientific judgement, independence, rigor, and thorough record-keeping. | 10/05/2025 |
| 403 | Veracyte South San Francisco, CA Specimen Processor Bachelor’s degree Exp: 0-2 years |
Primarily responsibility for receiving and accessioning specimens, handling specimen documentation, and data entry of requisitions. They are also responsible for keeping the lab in a clean and orderly condition. Specimen Processor I are knowledgeable in sample integrity issues and are a resource to others in the lab. They maintain flexibility regarding work schedules including daily assignments, holiday schedules, and days of the week as determined by business need. | 10/05/2025 |
| 404 | Vertex Boston, MA Process Dev Engineering Scientific Associate Bachelor's degree in Biochemistry, Biological Engineering, Chemical Engineering or a related field Exp: 1 year |
Supports the development of upstream or downstream production processes for cell therapy projects. Supports technology transfer to CMO and provides manufacturing support for GMP production. Supports a fully integrated team to facilitate the success of projects. Utilizes understanding of principles of molecular and cell biology techniques when troubleshooting typical problems. Applies statistical principles to guide process optimization. Conducts cell culture experiments, characterization and data analyses in support of process characterization and improvement. Supports technical reports, regulatory filings, source documents, patents and external publications. Works within departmental teams, supports deliverables and participates in team discussion on issue resolution. | 10/05/2025 |
| 405 | VGXI The Woodlands, TX Quality Control Technician Bachelor’s Degree Exp: 1-3 years |
The Quality Control Technician is responsible for in-process and release testing of products manufactured at VGXI. Will provide support for new assay development, method transfers, risk assessments, assay qualifications, change controls and validations. Set-up, organization, and day-to-day operations of a Quality Control Lab are also required. | 10/05/2025 |
| 406 | Viatris St. Albans, VT Chemist SI, Quality Control Bachelor's degree Exp: 0-2 years |
Performs and documents the analysis of samples following approved test methods. Calculate, check, and/or review data. Assist with method development, validation, and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 10/05/2025 |
| 407 | Vivex Biologics Miami, FL Quality Control Labeling Inspector Bachelors Exp: 0-1 years |
The QC Labeling Inspector is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Performs final product labeling and inspections, manages transport and storage of quarantine tissue, and maintains labeling supplies. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Promotes Usage of Problem Solving. Ensure that Labeling Operations are in Compliance with the State and Federal Regulations and AATB Standards. | 10/05/2025 |
| 408 | Vivex Biologics Miami, FL Process Engineer I BS or MS in Biomedical, Mechanical or Industrial Engineering or other applicable engineering discipline Exp: 1-3 years |
The Process Engineer I is responsible for evaluating and improving manufacturing processes to reduce cost, improve yields, and reduce variation. This position performs new process design and implementation, process validations and process qualifications. Process Engineers also participate in technology transfer to ensure the processes necessary for new products are effectively translated to manufacturing from R&D. Process Engineer I makes use of statistical analysis methods, critical thinking, process development, and scaling principles to achieve the objectives mentioned above. | 10/05/2025 |
| 409 | Waters Corporation Milford, MA Supplier Quality Engineer I bachelor’s degree in engineering, Mathematics, Business, Science, or related experience in a technical field Exp: 1-2 years |
Waters Corporation is currently seeking a Supplier Quality Engineer I to join our organization. This position is hands-on in a fast-paced environment which will interact with external suppliers and multiple internal functions (R&D, Engineering, Test Engineering, Reliability Engineering, Regulatory, Purchasing, sister manufacturing sites and contract manufacturers) to resolve supplier quality issues. Primary responsibilities will be to analyze and measure supplier performance, implement corrective actions when needed, and draft quality agreements with suppliers to define the requirements between the supplier and Waters. Responsibilities include supplier investigations into product non-conformances, reporting quality system metrics, supporting Statistical Process Control (SPC) initiatives, and driving projects related to product and process quality. The position is also responsible for performing quality audits on suppliers to ensure adherence to Waters expectations. Supplier Quality Engineers act as liaison for quality issues between our production areas, and our RDE, sustaining & test engineering departments and suppliers. | 10/05/2025 |
| 410 | West Kinston, NC Associate Process Engineer, Sterilization Bachelor’s or Master degree in Biology/ Microbiology /Chemistry or another scientific area Exp: 1-3+ years |
This role is key to developing and introducing process improvements, standards, life cycle management and validation in select process areas, helping to advance and transform West’s growing business, supporting capital investments and contributing to addressing complex assignments. This person has decision rights for his process area, and he/she will have the opportunity to drive the implementation of new innovative processes and technologies in cooperation with the engineering and quality assurance teams and the plants. | 10/05/2025 |
| 411 | WuXi AppTec Middletown, DE QC Operation Specialist Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or related discipline Exp: 1-3 years |
We are seeking a QC Operation Specialist to provide critical operational support to the QC laboratories at WuXi STA’s Middletown, DE site. This role is responsible for stability room and equipment management, sample logistics, and controlled documentation, ensuring QC laboratories operate efficiently, meet testing timelines, and remain in full compliance with GMP and regulatory requirements. The QC Operation Specialist will be a key contributor during both startup and steady-state operations, supporting Analytical and Microbiology QC teams. | 10/05/2025 |
| 412 | WuXi Biologics Cranbury, NJ Process Equipment and Reliability Engineer I Bachelor’s degree in mechanical, Chemical, Bioprocess, or related Engineering discipline Exp: 0-2 years |
The Process Equipment and Reliability Engineer I will provide technical support to ensure safe, reliable, and compliant operation of process and utility equipment within a biopharmaceutical manufacturing facility. An Engineer I, will assist with troubleshooting, preventive maintenance, and reliability initiatives while working within cGMP requirements, engineering systems, and reliability methodologies. This role is designed to build foundational skills in equipment engineering and reliability while contributing to daily operations and long-term asset improvement efforts. | 10/05/2025 |
| 413 | Veranex Providence, RI Manufacturing Engineer 1 or 2 Bachelor’s degree in manufacturing or mechanical engineering Exp: 1-3 years |
Veranex has an exciting opportunity to join our team as a Manufacturing Engineer 1 or 2. You will be part of a team working to improve lives globally through medical technology innovation. Manufacturing Engineer 1 or 2 performs and coordinates broad manufacturing engineering activities in the development and supply of capital and disposable medical devices and instruments. | 10/05/2025 |
| 414 | Abbott Sylmar, CA Software Engineer I Bachelors Degree in Computer Science, Engineering, Mathematics, or related field Exp: 0-2 years |
This Software Engineer I position is on the Digital Health Engineering team in Abbott’s Cardiac Rhythm Management division, and works on-site in Sylmar, California. The Digital Health Engineering team is responsible for developing, maintaining, and leveraging software solutions to provide internal and external stakeholders with the data and resources they need to effectively manage patient care, optimize clinical therapies, and improve product performance. Members of the Digital Health Engineering team are expected to translate complex customer and business needs into data-driven technical solutions. This role requires a blend of strong technical and software engineering skills, problem-solving abilities, customer centricity, as well as creativity, strong communication skills, and an entrepreneurial mindset. | 10/05/2025 |
| 415 | Abbott Temecula, CA Manufacturing Process Engineer Bachelor's Degree Exp: 1 year |
The Associate Manufacturing Engineer will serve as the primary manufacturing engineer supporting operations in Abbott Vascular Temecula. The individual performing this role will have to integrate with the team supporting the manufacturing line including but not limited to: the line supervisor, Quality Engineer and operators to address the opportunities found in their assigned manufacturing line. They will be accountable for quality, safety, product output and yield for their assigned manufacturing line. This person may also have a contributing role as a sustaining engineer for the department. | 10/05/2025 |
| 416 | Abbott Sturgis, MI Quality Engineer Master's Degree Exp: 1-3 years |
The Quality Engineer is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support. | 10/05/2025 |
| 417 | Abbott Sylmar, CA Test Development Engineer I Bachelors Degree in Electrical engineering or related engineering field Exp: 6 months |
This Test Development Engineer I position works out of our Sylmar, CA location in the Cardiac Rhythm Managment Division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Test Development Engineer assists with designing and developing non-product software and hardware to test new products. Test Development Engineer investigates and resolves production problems involving test equipment, software, and hardware. You will apply engineering and scientific principles to evaluate and solve technical problems. Remain abreast of and consults on technological advancements. Identify and routinely uses the most effective, cost-efficient, and best practices to execute processes; continually evaluates their effectiveness and appropriateness. | 10/05/2025 |
| 418 | Abbott Sylmar, CA Associate Supplier Quality Engineer Bachelors Degree in Engineering or Technical Field Exp: 0-2 years |
Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements. Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements. Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues. Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Design and conduct experiments for process optimization and/or improvement. Appropriately document experiment plans and results, including protocol writing and reports. Lead process control and monitoring of CTQ parameters and specifications. Lead and implement various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing). Lead the investigation, resolution and prevention of product and process non-conformances. Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member). Lead in the completion and maintenance of risk analysis. Work with design engineering in the completion of product verification and validation. Work with microbiology to ensure appropriate environmental monitoring and that microbiology requirements are considered in product and process development activities. Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. | 10/05/2025 |
| 419 | Abbott Alameda, CA Specialist Quality Assurance Bachelors Degree Exp: 1+ years |
The Specialist Quality Assurance Engineer will analyze quality standards for components, materials or services. You will apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met. | 10/05/2025 |
| 420 | Abbott St. Paul, MN Supplier Quality Engineer Bachelors Degree Exp: 1-3 years |
Ability to effectively communicate, facilitate and organize project activities relating to ensuring supplier quality. Develops and manages project schedules to ensure deadlines are met. Serves as the primary Quality contact for suppliers and provides technical assistance to management for suppliers as requested. Works with supplier development engineering to performs on-site annual and critical component supplier audits to ensure compliance with Quality Systems procedures and CSI requirements. Generates audit reports and ensures supplier audit findings are tracked to timely and closure. Provides quality systems input to suppliers such as, but not limited to: statistical process control, gage R&R studies, and capability studies. Resolves supplier quality issues at incoming inspection and the production line. Provides project team leadership and conducts investigations relating to supplier quality issues. Completes non-conforming material reports (NCMR), supplier requests for change (SRC), supplier corrective action requests (SCARs) and monitors follow-up with assigned supplier base. Routinely reports on supplier performance per defined metrics to management and other team members. Represent Quality during audits and interface with FDA, ISO, or any external auditor. | 10/05/2025 |
| 421 | AbbVie Irvine, CA R&D Engineer II Master’s Degree in Industrial and Systems Engineering, Mechanical Engineering, Biomedical Engineering, or a related field Exp: 1 year |
Contribute to the development and launch of new drug/medical device combination products. Independently design, execute, and interpret novel engineering research and development. Generate and lead new engineering proposals. Investigate, identify, develop, and optimize new test methods and techniques and set and meet experimental timelines. Innovate and implement new experimental protocols. Act as a critical contributor to feasibility, development, and verification testing stages of product development through creation and release of new test methods, as well as design verification plans, protocols, records, and reports. Effectively organize and present scientific plans and data. Contribute to writing and conceptual framework of publications, presentations, and patents. Act as a resource or mentor for others. | 10/05/2025 |
| 422 | AbbVie South San Francisco, CA Associate Scientist II - Cell Line Development MS Exp: No exp |
The Cell Line Development Group in South San Francisco, CA is seeking an Associate Scientist II to join a talented and collaborative team developing CHO cell lines for GMP applications. In this laboratory position the candidate will perform hands-on CHO cell line development for pipeline assets and support the establishment of automation capabilities in the group to increase throughput. The successful candidate will contribute to the evaluation and implementation of an automated liquid handler for cell culture workflows. | 10/05/2025 |
| 423 | Abeona Therapeutics Cleveland, OH Quality Control Analyst I (QC Analytical) BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 1-3 years |
The Quality Control Analyst I performs routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Testing includes qPCR, immunostaining, protein characterization and product specific analytical test methods. Interacts with employees internal and external to Quality Control. | 10/05/2025 |
| 424 | Abeona Therapeutics Cleveland, OH Specialist I, Quality Assurance - Quality Operations Bachelor's degree in related field Exp: 1 year |
The Specialist I, Quality Assurance performs routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the maintenance of the quality systems in support of a cGMP Operation for Manufacturing logistics processes relating to Abeona Manufactured Media batch record review and release from start to end of manufacturing activities, in-process sampling / testing, autoclave, and document management ensuring procedural and regulatory compliance throughout the manufacturing process. The Specialist I, Quality Assurance will report to the Associate Manager, Quality Assurance or above and will support manufacturing and quality control as the production area Quality Assurance representative. | 10/05/2025 |
| 425 | AstraZeneca Frederick, MD Specialist I Quality Control BS degree Exp: 0-5 years |
In this role, you will perform selected analytical quality control testing activities, including HPLC, GC, and UPLC testing. You will be responsible for conducting in-process and finished product testing according to standard operating procedures. Your duties will include completing documentation supporting testing procedures, maintaining lab instrumentation, and ensuring supply levels are adequate. You will read, understand, and follow SOPs while complying with cGMPs. Critical thinking and problem-solving will be key as you apply knowledge of good manufacturing and laboratory practices daily. Safety is paramount, and you'll adhere to company safety procedures and guidelines. Depending on your demonstrated ability, you may assist in executing protocols and laboratory studies required to support QC investigations, method validation, and stability studies. | 10/05/2025 |
| 426 | AstraZeneca Gaithersburg, MD Scientist, Oncology TCR-T Cell Therapy Master’s degree in Immunology, Cancer Biology, Cell Biology, or relevant scientific field Exp: 1 year |
We are seeking a highly motivated and independent Scientist to join our rapidly growing Cell Therapy Team. In this role, you will contribute to advancing innovative Cell Therapy products by designing and conducting laboratory experiments, developing methodology, and generating and interpreting scientific data in a highly collaborative environment.Expertise inin vitro and in vivo studies and T cell biology is critical for this role. To be successful in this role, you must be well-organized and keep an excellent written record of your work. You will be based in Gaithersburg, MD and report to the Associate Director, TCR-T Cell Therapy. | 10/05/2025 |
| 427 | Adare Vandalia, OH Analytical Scientist Master’s Degree in Chemistry or related discipline Exp: 0-1 years |
The Analytical Scientist will support the development and validation of analytical methods for raw materials, work-in-process, and finished products to provide testing support for the formulation development and clinical supplies release process. The Scientist will also be expected to provide some training, coaching, and mentoring for more junior scientists. | 10/05/2025 |
| 428 | Adicet Bio Redwood City, CA Manufacturing Associate 2 – Cell Therapy Bachelor’s degree in biological sciences, engineering, or related discipline Exp: 1-2 years |
We are seeking a highly motivated and detail-oriented individual with a strong background in cell process development and/or manufacturing. The Manufacturing Associate II will report to the Director of Manufacturing and play a key role in supporting daily GMP manufacturing operations for allogeneic CAR T cell therapies. | 10/05/2025 |
| 429 | ADMA Biologics Boca Raton, FL QA Specialist I - Manufacturing Oversight Bachelor's Degree Exp: 1-3 years |
The QA Specialist I - Manufacturing Oversight performs manufacturing oversight activities to ensure compliance with policies and procedures. Oversight activities include, but are not limited to, real-time manufacturing batch record review, review of manufacturing documentation (logs, charts, etc.), and resolution of issues on the manufacturing floor. | 10/05/2025 |
| 430 | ADMA Biologics Boca Raton, FL Microbiologist I, Quality Control B.S. in Biological Science or related science discipline Exp: 0-3 years |
Perform environmental monitoring and water sampling within the controlled manufacturing areas and QC Laboratory. | 10/05/2025 |
| 431 | Agilent Newport, DE Capital Projects Engineer Bachelor’s degree in Mechanical, Electrical, or Chemical Engineering Exp: 1+ years |
Join a team that’s advancing innovation in life sciences. At Agilent, we empower our engineers to drive impactful change through smart design, efficient processes, and collaborative problem-solving. We’re looking for a Manufacturing Engineer to support our LC Column Manufacturing operations, with a focus on capital project execution, equipment optimization, and continuous improvement. | 10/05/2025 |
| 432 | Agilent Remote, CA Field Service Engineer - Pathology Bachelor’s or Master’s degree in a scientific field (e.g., Chemistry, Biochemistry, Biotechnology, Analytical Chemistry) Exp: 1+ years |
Join Agilent as a Field Service Engineer – Pathology and play a critical role in supporting scientists and healthcare professionals in delivering life-enhancing discoveries. In this dynamic role, you will provide on-site technical support, ensuring the optimal performance of Agilent’s pathology solutions. Your expertise will directly impact laboratories by minimizing downtime, optimizing efficiency, and enhancing customer success. | 10/05/2025 |
| 433 | Agilent Boulder, CO Manufacturing Associate 2 – Cell Therapy Bachelor’s or Master’s Degree Exp: 0-1+ years |
As a Manufacturing Associate, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. Responsible for performing a variety of support duties in one or more manufacturing areas. Duties may be related to cleaning, ordering, stocking, preparing, installing, maintaining, repairing and supporting manufacturing equipment and processes, Assistance with validation protocol execution, product test and troubleshooting, and technical analyses and problem-solving, Performs daily cleaning activities and maintains production areas in an audit ready, neat, clean and orderly state. You will have an opportunity to become skilled in the use of a wide range of lab instruments which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are critical. | 10/05/2025 |
| 434 | Agilent Los Angeles, CA Field Service Engineer - GC/GCMS Bachelor's or Master's Degree within the science field Exp: 1+ years |
As a Field Service Engineer for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software and consumables is key. Applying your communication skills, creativity and can-do attitude is essential. The ability to help with solving customer problems and a commitment to deliver the highest levels of customer service is how you will build customer success. | 10/05/2025 |
| 435 | Agilent Frederick, CO Validation Engineer Bachelor’s or Master’s degree Exp: 1-2+ years |
Performs cleaning validation and equipment commissioning and validation engineering duties to support initial start-up and qualification of a new Active Pharmaceutical Ingredient (API) manufacturing facility at Agilent Technologies Nucleic Acid Solutions Division in Frederick, Colorado. Primary responsibilities include the execution, reporting, and communication of validation activities compliant with pharmaceutical Good Manufacturing Practices (GMP). | 10/05/2025 |
| 436 | Agilent Carpinteria, CA Engineer - Manufacturing Systems (MES) Bachelor’s or Master’s degree or equivalent experience in Engineering Exp: 1+ years |
Join Agilent’s innovative manufacturing team and help craft the future of smart, compliant, and efficient production systems. As a Manufacturing Systems Engineer, you’ll chip in to the development and optimization of digital manufacturing solutions, ensuring flawless integration of software, equipment, and processes across regulated environments. | 10/05/2025 |
| 437 | Forge Biologics Columbus, OH Analytical Quality Control, Analyst I (2nd Shift) Bachelor’s degree in biology, molecular biology, virology, biochemistry or related discipline Exp: 0-4 years |
We are currently seeking a Quality Control (QC) Analyst I, Analytical Testing, to join the Forge Biologics team. This role will perform characterization and release testing QC for AAV vectors, plasmids, and cell banks, while maintaining meticulous records and ensuring the accuracy of data for all products. This position is responsible for routine test method execution, assisting in method qualification and validation, instrumentation troubleshooting, and data analysis. The ideal candidate will be skilled in technical problem-solving and laboratory techniques to support our growth in the Gene Therapy sector. The Analyst I role offers an excellent opportunity to gain hands-on experience in the field of gene therapy. | 10/05/2025 |
| 438 | Forge Biologics Columbus, OH Lab Coordinator Bachelor's degree in scientific discipline (Biology, Chemistry, or related field) Exp: 1-3 years |
The Laboratory Coordinator, QC Analytical Testing is responsible for day-to-day coordination of laboratory operations to ensure that QC spaces are well-maintained, and compliant with GMP expectations. Key responsibilities include oversight of laboratory cleaning and 5S activities, support for equipment calibration and preventive maintenance (PM), pipette verifications, and sample shipment for external testing. This role will work closely with the Laboratory Manager and QC staff to support smooth laboratory operations and execution of GMP testing. | 10/05/2025 |
| 439 | Alamar Fremont, CA Associate Scientist II – Technology Access Program Master’s degree in Immunology, Neuroscience, Biochemistry, or a related discipline Exp: 1-2 years |
We seek a highly motivated Associate Scientist to join a dynamic team of professionals in the Technology Access team to support our company mission. In this role, you will work cross-functionally across multiple teams including R&D, Sales and Marketing to design, execute and deliver NULISA immunoassay collaboration projects as part of the Technology Access Program. An ideal candidate will have a background in proteomics and bring hands-on experience in sequencing workflows, NGS library preparation, and automated liquid handling instruments. The ability to manage multiple projects in a fast-paced, collaborative environment is highly preferred. | 10/05/2025 |
| 440 | Alcami Morrisville, NC Scientist II - Compendial Testing, Raw Materials Masters degree in Chemistry, Biochemistry, or related field Exp: 0+ years |
The Scientist II (Chemistry) is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, TOC, UV, osmolality, density, titration and pH are commonly employed in the described testing in addition to other key methodologies such as KF, CCIT and HPLC. Test methods employed may be compendial (i.e. USP, EP, JP) or proprietary (client supplied or developed by The Company) and may also assist with method verification / method validation projects as needed. | 10/05/2025 |
| 441 | Alcami Morrisville, NC Quality Specialist - GMP Master’s degree in Chemistry, Biology, or relevant field Exp: 1+ years |
The Quality Specialist will provide site quality support in a fast-paced environment by effectively performing activities of substantial variety to ensure quality and compliance with applicable regulatory requirements and is proficient in all document and protocol approvals applicable to the respective processes executed at the respective lab or manufacturing facility. These activities include reviewing documents and data, supporting audits and inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist serves as quality host for client and regulatory agency audits and inspections. The position develops SOPs or other quality documents as needed. | 10/05/2025 |
| 442 | Shimadzu Virtual, NJ Field Service Technician I AA EE or similar, BS preferred Exp: 1 yr |
Provide daily repair and maintenance support for assigned products, including installations; Conduct in-house bench repairs and onsite customer repairs as needed while primarily handling field service calls with limited supervision; Travel within the local region (including day and overnight trips) to support customer needs; Offer technical support via phone to customers and field personnel regarding repairs, maintenance and installations. | 10/01/2025 |
| 443 | Spear Bio Woburn, MA Associate Scientist/Senior Associate Scientist, Assay Development MS in Biology, Biochemistry, Biomedical Engineering or a related discipline Exp: 1-2+ years |
We are seeking a highly motivated and experienced Associate Scientist/Senior Associate Scientist to join our Assay Development team, with hands-on experience in developing and validating ultrasensitive immunoassays. The ideal candidate will support the full lifecycle of assay development, from initial concept and research to validation and assay transfer. This individual will play a pivotal role in advancing Spear Bio’s new range of ultrasensitive immunoassays and assay biomarker programs. This role is based onsite in our lab in Woburn, MA 5 days/week. | 09/29/2025 |
| 444 | SRI Palo Alto, CA Mechanical Engineer Bachelors in Mechanical Engineering or a related field Exp: 1+ years |
The Bright Ceramics Technology group (BCT) is focused on developing, applying, and commercializing a unique technology platform based upon advanced materials. They develop and manufacture cutting-edge components and systems. BCT is currently searching for new grad Mechanical Engineers to join their team. The ideal candidates will be able to perform basic engineering analysis, complete detailed specifications, and be able to build and troubleshoot systems with minimal supervision. Working with interdisciplinary teams, the ME will apply their knowledge of mechanical design and materials properties to invent, fabricate, and test complex components and systems that are benchmarks of elegant and effective design. Successful applicants will be proficient in mechanical design and analysis, prototyping, a wide range of manufacturing processes, electro-mechanical systems, 3D CAD, and system fabrication. | 09/29/2025 |
| 445 | Stallergenes Greer Lenoir, NC Validation Engineer Bachelors degree in a scientific field Exp: 1-2 years |
Independently plan, perform and/or coordinate validation projects to ensure timely completion. Draft and coordinate execution of process validation and equipment qualifications (IQ, OQ, PQ, FAT’s, SAT’s). Draft/or provide technical guidance for SOPs and other master documents. Remain current with industry and regulatory agency trends. Keep Tech Ops Management informed of the status of validation activities and projects. Support Engineering and Operations in the development of critical process parameters. Provide technical leadership for deviation investigations. Analyze data and provide recommendations for improvements in manufacturing process, and equipment. Prepare and execute protocols, Engineering Studies, and other technical documents, and participate in the interpretation of data, collaborating with other departments. Own and Execute Audit Role as the Support / Research SME collecting data to support Audit Requests for the Validation/Calibration Department for all areas of validation. Other responsibilities as directed. Conduct peer-review of protocols and reports. Position may require occasional travel and working with validation consultants and the validation team located at the North Carolina site | 09/29/2025 |
| 446 | Stallergenes Greer Lenoir, NC Chemist I Bachelor degree in Science /preferably in Chemistry Exp: 0-2 years |
Analysis of allergenic extracts by Elisa, RID and IEF. Analysis of preservatives phenol and glycerin by HPLC. Wet chemistry analysis specific gravity, identifications, USP and EP compendia and WFI analysis. Operates laboratory instrumentation as FTIR, GC, HPLC and others | 09/29/2025 |
| 447 | Steris Cooper City, FL Quality Engineer BS Engineering in related technical field Exp: 1+ years |
The Quality Engineer in our Cooper City, Florida facility is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. As a Quality Engineer, you will support complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 09/29/2025 |
| 448 | Steris Whippany, NJ Quality Analyst Bachelor’s degree in Scientific or Technical Field Exp: 1 year |
The Quality Analyst in the STERIS Applied Sterilization Technologies (AST) Whippany, New Jersey location is responsible for assisting in administration of the quality management system to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 09/29/2025 |
| 449 | Sterling Pharma Solutions Germantown, WI Analytical R&D Associate Scientist Master’s degree in a scientific discipline such as analytical chemistry, or related field Exp: 0-2 years |
As the Analytical R&D Associate Scientist, you are accountable for driving results by supporting manufacturing activities through phase specific method development and method validation activities. The Analytical Scientist will execute the development of analytical methods and improve existing methods to support our active pharmaceutical ingredients development program. The Associate Scientist II works closely with a multifunctional team to support quality control and chemical research and development groups. | 09/29/2025 |
| 450 | Sterling Pharma Solutions Germantown, WI Analytical Chemist Bachelors Degree in Chemistry or related field Exp: 0-2 years |
As the Analytical Chemist at Sterling, you will be accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. Testing performed directly supports manufacturing through the release of raw materials, intermediates and API’s; as well as in-process controls, equipment cleaning verification, reference standard qualification, and stability program. The Analytical Chemist will develop the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data working. | 09/29/2025 |
| 451 | Sterling Pharma Solutions Germantown, WI Associate Scientist Bachelor’s degree in Chemistry or related field Exp: 0-2 years |
The Associate Scientist, under the direction of a senior scientist, executes chemical reactions on a gram to multi-kilogram scale and performs routine analytical procedures to monitor reaction progress. This role requires the incumbent to efficiently organize routine work with supervision and properly evaluate and interpret generated data. The Associate Scientist will exercise judgment within defined procedures and practices to determine appropriate action. The position requires superior leadership behaviors of the Sterling core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 09/29/2025 |
| 452 | Stryker Portage, MI Electrical Design Engineer, R&D Bachelor's degree in EE or related discipline Exp: 0+ years |
Are you a passionate electrical engineer with a desire to innovate and shape the future of healthcare? Join our forward-thinking medical device team in our Surgical Technologies business unit, working specifically on developing our Next Generation Neptune portfolio, where your work will directly impact patient outcomes. As a key contributor, you will independently design and develop advanced electrical components and sub-systems for groundbreaking medical devices, using cutting-edge techniques in circuit design, testing, and problem-solving. | 09/29/2025 |
| 453 | Supernus Pharmaceuticals Rockville, MD Chemist Analytical Sciences PA Bachelor’s degree in life sciences (Chemistry degree is preferred) Exp: 0+ years |
The Chemist Analytical Sciences PA will provide analytical support for pharmaceutical solid dosage forms primarily by using dissolution testing, spectroscopy, HPLC, wet chemistry, including maintaining proper documentation. | 09/29/2025 |
| 454 | Syner-G BioPharma Group Worcester, MA Project Engineer Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 09/29/2025 |
| 455 | Syner-G BioPharma Group Norwood, MA Sr. Project Engineer Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Sr. Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 09/29/2025 |
| 456 | Syner-G BioPharma Group Boston, MA Associate Facilities Engineer Bachelor’s degree in a related field Exp: 0-2 years |
We are seeking a Facilities Engineer with experience in the management, execution, and day-to-day support of building and plant operations, including labs, manufacturing plants, utilities, equipment, and systems. The ideal candidate will perform routine inspections, maintain documented records, and be on-call for emergencies, ensuring compliance with regulatory requirements and GMPs. Effective communication and collaboration with various departments are essential to meet the facility’s needs and quickly resolve any issues. | 09/29/2025 |
| 457 | Syner-G BioPharma Group West Warwick, RI Project Engineer (1st & 2nd Shift) Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 09/29/2025 |
| 458 | SystImmune Redmond, WA Research Associate/Senior Research Associate BS or MS in immunology, biochemistry, molecular biology, structural biology, or a related field Exp: 1+ years |
We are seeking a skilled Research Associate/Senior Research Associate with experience in utilizing display technologies (yeast/phage) in protein engineering, directed evolution, or binder discovery. This is a laboratory-based role that will be supporting protein engineering efforts in discovering novel binders and novel protein leads/scaffolds. The position will join a growing protein engineering team in an innovative organization and reports to the Director of Protein Engineering. The ideal candidate will be a quick learner with a broad experience set with direct expertise in a display technology and/or an adjacent field including but not limited to high throughput molecular biology, antibody/binder discovery, and protein engineering. Industry experience in biologics drug development is required. | 09/29/2025 |
| 459 | SystImmune Redmond, WA Research Associate/Senior Research Associate - Cell Science Bachelor’s degree in biology or a related science major Exp: 1+ years |
Located in Redmond WA, Systimmune Inc.is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic multi-specific antibodies, as well as antibody-drug conjugates (ADCs). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. We are seeking a Research Associate / Senior Research Associate with experience in cell culture and plasmid preparation to join our Cell Science Department. | 09/29/2025 |
| 460 | Takeda Social Circle, GA Engineer I Bachelor’s degree in Engineering or a related field Exp: 1 year |
Join Takeda as an Engineer I where you will provide process support to the Fractionation manufacturing group by solving technical issues within the Social Circle Fractionation manufacturing facility. You will assist your quality and manufacturing partners in maintaining process compliance, aiding in the implementation of yield and process improvements, and supporting process validation activities. As part of the Fractionation Manufacturing Sciences team, you will report to the Associate Director of Manufacturing Sciences, Fractionation. | 09/29/2025 |
| 461 | Tanvex Biopharma San Diego, CA Manufacturing Technician I, Production Support Bachelor's degree in EE or related discipline Exp: 0-3 years |
Under supervision, the Manufacturing Technician, Production Support, will perform routine manufacturing activities in GMP manufacturing areas, solution preparation, dispensing raw material, bioprocessing support and autoclave operation. Operations will be performed according to Standard Operating Procedures (SOP), Work Instructions (WI) and Master Batch Records (MBR). Perform manufacturing steps, execute routine MBRs, and revise documents such as MBRs and SOPs as needed. Flexible shift schedules and overtime may be required. | 09/29/2025 |
| 462 | TE Connectivity Middletown, PA Quality & Reliability Engineer I Masters degree in Industrial or Mechanical engineering Exp: 1-2 years |
Interact with cross functional team members to plan product development activities in support of project requirements and customer needs. Participate in all activities impacting customer requirements including DFMEA, Design Reviews, and Design for Manufacturing Reviews. Take hands on personally committed approach to the Quality feedback loop including resolving customer complaints and plant issues plus line concerns. Participate in development of PFMEA. Responsible for development of Control Plans/Inspection Plans, First Article Inspection and Capability Study planning and acceptance for new or revised tooling, PPAP or other customer required documentation. Create, and Safe Launch plans to help ensure that all production risks are addressed throughout the Project lifecycle. Support all activities relating to the refinement/improvement and creation of process from a quality perspective. Management of internal and external suppliers from a quality perspective. Perform failure analysis using 8D format to clearly define the problems, scope, root cause and corrective actions. Interface with supplier quality engineering as needed to coordinate actions related to supplier process design, inspection and non-conforming materials. Travel as required to ensure project success. This position will have global responsibilities requiring flexible working. Employee must perform his/her job within acceptable safety, environmental, quality, productivity and performance standards as outlined in local and global policies and handbooks. Transmission of customer specific requirements and Quality Manuals into the Project/Product. Risk estimation and mitigation through Project lifecycle using clearly defined and constantly improved measurables including escalation as required. | 09/29/2025 |
| 463 | TE Connectivity Northborough, MA EH&S Analyst II BA/BS Degree in, Environmental Engineering, Environmental Studies , Industrial Engineering or related major Exp: 1-3 years |
Assists in ensuring and monitoring safety in the workplace including the application and communication of health, safety and hazardous material standards, procedures and practices consistent with established company, environmental and government regulations | 09/29/2025 |
| 464 | Tempus Chicago, IL Molecular Technologist I (Extractions) BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 0-1+ years |
Work with a cutting-edge genomics workflow to provide high-quality data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform nucleic acid extraction and DNA/RNA quantification and qualification using robotics and automated liquid handlers. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/29/2025 |
| 465 | Tempus Research Triangle Park, NC Quality Control Technologist I-III BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work within a cutting-edge genomics workflow to provide equipment quality control support in a high-volume clinical molecular laboratory. Help create and implement new equipment functionality for use by Tempus R&D and clinical lab staff while maintaining CLIA/CAP/ISO compliance. Complete Performance Qualifications (PQs), Preventive Maintenance (PM), relocation, and routine maintenance for all clinically approved molecular laboratory equipment. Collect and help analyze metrics. Investigate equipment related issues and help facilitate and implement corrective and preventative actions. Interact with lab management and personnel to provide training, troubleshoot issues, and prioritize QC tasks. Report significant findings/deviations and system deficiencies to lab management, as appropriate. Update SOPs and equipment records within the document control system, including creation/ revision/ review of internal SOPs and other quality documentation. Create and review protocols and qualification summaries. Support the Lab Facilities team with freezer defrosts and hazardous waste pick-up as needed. Monitor and respond to laboratory temperature excursions. | 09/29/2025 |
| 466 | Ritedose Columbia, SC Microbiologist II BS degree in Microbiology or related field Exp: 1 year |
The Microbiologist II is responsible for all duties related to performing environmental monitoring, personnel monitoring, microbial enumeration, microbial identification, and sampling of utilities. The Microbiologist I is also responsible for performing all the microbiological testing related to raw materials, utilities, and in-process product testing. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. | 09/29/2025 |
| 467 | Ritedose Columbia, SC Process Development Engineer BS degree in Chemical or Mechanical Engineering Exp: 1-3 years |
Process Development Engineer for Finished Packaging is responsible for designing and implementing Finished Packaging development for development products. The Engineer will design and implement appropriate change requests, packing studies, batch records, forms, procedures, work instructions, risk assessments, etc. as needed to achieve the development and production goals of the organization. The Engineer’s responsibility will include supporting other Formulation, Filling, Bulk Packaging development as assigned by management. | 09/29/2025 |
| 468 | Thermo Fisher Scientific Greenville, NC Formulation Technician II Bachelor's degree Exp: No exp |
As a Formulation Technician II, you will play a vital role in producing sterile injectables and working on moderate-scale problems that require analysis and critical thinking. You will follow written and verbal instructions to ensure that pharmaceutical products are manufactured in accordance with industry guidelines and regulations. | 09/29/2025 |
| 469 | Thermo Fisher Scientific Plainville, MA Technical Operations, Technical Writer II Bachelor’s degree Exp: 1-2 years |
As RSO, you’ll play a key role in supporting our GMP manufacturing operations by developing and maintaining high-quality documentation. Your work directly impacts the consistency, safety, and compliance of the treatments we help bring to market. | 09/29/2025 |
| 470 | Thermo Fisher Scientific Greenville, NC R&D Mfg Scientist II - Analytical Development Masters Degree in Chemistry, Biochemistry, Molecular Biology, or related physical/biological science field Exp: 1+ years |
Provides routine analyses in a biochemistry environment within defined procedures and practices. Performs analytical methods for moderately sophisticated testing on samples, stability, and production intermediates to support process development and/or manufacturing operations. May research and implement new methods and technologies to improve operations. Makes detailed observations and reviews, documents, and communicates test results. | 09/29/2025 |
| 471 | Thermo Fisher Scientific Wilmington, DE Associate Scientist, Purification Process Science BS degree in biochemistry, bioengineering, biology, chemistry or related fields Exp: 0-1+ years |
Our client is seeking a motivated and dedicated protein purification scientist to support protein purification process development and optimization primarily for novel therapeutic monoclonal antibody products including bispecifics throughout all stages of clinical trials. | 09/29/2025 |
| 472 | Thermo Fisher Scientific Greenville, NC QC Scientist I Bachelor’s degree in a biology/related field Exp: 1+ years |
A successful person will perform Environmental Monitoring tasks in support of Steriles production within classified areas. The individual is encouraged to follow the 4i Values that are held in high regards by the company when completing their work. The four values are integrity, innovation, intensity, and involvement. The job function includes aseptic technique which requires the individual to gain knowledge of aseptic gowning as well as working in cleanrooms in order to monitor the area while sterile products are filled and manufactured. | 09/29/2025 |
| 473 | Thermo Fisher Scientific Boston, MA Labs FSP Scientist - GMP, Chemistry Master's degree in a scientific discipline Exp: 0-2 years |
As a Scientist, you provide technical support for Release and Stability Laboratory (RSL) department supporting method validations, investigations, reference standard and external testing. Specific assigned persons are responsible to ensure activities occur in an efficient and cGMP compliant manner while fostering the customer's vision and values. | 09/29/2025 |
| 474 | Thermo Fisher Scientific Greenville, NC QC Scientist I, QC Steriles Bachelor’s degree in life science, preferably in Chemistry Exp: 1 year |
Perform analyses in a chemistry environment within defined procedures and practices. Perform analytical methods for moderately to complex testing on a variety of cleaning, in process, stability, and release samples. Support internal manufacturing operations. Make detailed observations and review, documents and communicate test results; recommend solutions. | 09/29/2025 |
| 475 | Transpire Bio Sunrise, FL Pharmaceutical Manufacturing Process Associate Scientist I/II BS or MS Degree in Chemical/Biochemical Engineering, Chemistry, Biochemistry or a related scientific discipline Exp: 0-5 years |
In this role, the Process Associate Scientist I/II will involve developing and optimizing pharmaceutical manufacturing processes, ensuring product quality and consistency, and complying with regulatory requirements on commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts pilot scale manufacturing activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. | 09/29/2025 |
| 476 | Tri-Pac South Bend, IN Lab Technician Bachelor’s degree in a scientific field Exp: 1-2 years |
The Lab Technician performs chemical analysis and testing on chemical raw materials and in-process/finished batches according to methods and specifications as defined by the customer. He/she assists with compiling, analyzing and interpretation of results as well as maintaining the flow of samples and paperwork through the laboratory. The Lab Technician maintains laboratory equipment and instrumentation to ensure ideal usage and has a strong attention to detail. The Lab Technician is able to effectively correspond with internal customers, has excellent organizational skills, able to perform physically demanding work such as moving and lifting equipment and capable of standing for long periods of time. | 09/29/2025 |
| 477 | Twist Bioscience Quincy, MA Research Associate II, Antibody Characterization Master’s degree in molecular biology, biochemistry, or a related discipline Exp: No exp |
We are seeking a motivated individual to join our team and expand our antibody characterization department. Using state-of-the-art technologies and workflows, this Research Associate would work with the Antibody Characterization team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns and contract services. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 09/29/2025 |
| 478 | Twist Bioscience Quincy, MA Research Associate II, Protein Analytics Master’s degree in molecular biology, biochemistry, or a related discipline Exp: No exp |
We are seeking a motivated individual to join our team and expand our bioanalytical department. Using state-of-the-art technologies and workflows, this Research Associate would work with the Protein Analytics team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns and contract services. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 09/29/2025 |
| 479 | Twist Bioscience South San Francisco, CA Research Associate II - R&D M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field Exp: 1-2 years |
As Research Associate II, you will work on new product development and existing process improvement. Your work will be mainly at the bench, however, you will have the opportunity to use high-throughput robotic instruments as well as bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 09/29/2025 |
| 480 | Unither Pharmaceuticals Rochester, NY Laboratory Application Scientist Master’s degree in life science such as Biology, Pharma Sciences, Analytical Sciences, or closely related discipline Exp: 1-3 years |
The Laboratory Application Scientist ensures that all laboratory systems composed of equipment, instruments and computerized systems are properly maintained, qualified, calibrated and secured to be properly used by the laboratory users to ensure a high level of confidence with product results. Provide access management for each computer system, while ensuring data handling and data integrity meet internal SOP and FDA requirements. This position is partnered with the laboratory system owners and the IT group. Ensuring all laboratory systems are properly used in chemistry and microbiology laboratories and assisting laboratory staff with technical issues and training. Provides recommendations on efficiency, new technology and best practices in the QC laboratories. | 09/29/2025 |
| 481 | Vantage MedTech Lenexa, KS NPI Engineer BS or MS degree in Engineering, preferably Mechanical or Manufacturing Engineering Exp: 1-3 years |
The NPI (New Product Introduction) Engineer will be responsible for ensuring that our innovative designs are transitioned into effective and sustainable production. Our life saving products are manufactured in Kansas City and require predictable delivery of high quality, cost-effective production over 5+ year product lifetimes. You will collaborate with Vantage MedTech’s Engineering and Manufacturing teams to provide input on the device design’s manufacturability, and plan and execute the transfer of these new products to our manufacturing facility. You will be responsible for ensuring that robust manufacturing processes are created, updated and in compliance with company standards, ISO, and GMP as required. In addition, you will help drive improvement projects that impact quality and productivity. | 09/29/2025 |
| 482 | Vantage MedTech Lenexa, KS Design Quality Engineer Bachelor's degree in Engineering Exp: 1-3 years |
Vantage MedTech is seeking a Design Quality Engineer to serve as the cornerstone of Quality Assurance in cutting-edge design projects, ensuring they meet the highest standards of excellence and compliance. This role is responsible for maintaining alignment with the Vantage MedTech Quality Management System and design control processes, acting as the QA representative on assigned projects. This individual will enhance the capabilities of the design engineering team by overseeing the maintenance and compliance of the Design History File (DHF), Device Master Record (DMR), and document control processes, while upholding compliance assurance for external partners. | 09/29/2025 |
| 483 | RayzeBio Indianapolis, IN Operator – Isotope Production Bachelor's in a STEM Field Exp: 1-4 years |
The Operator – Isotope Production will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As Operator – Isotope Production, you will be instrumental in implementing a novel isotope production program that will manufacture the clinical and commercial scale radioisotopes for RayzeBio’s drug products. This individual will be part of a team responsible for producing RayzeBio’s radioisotopes under Good Manufacturing Practices (GMP). Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. The Operator – Isotope Production will report directly to the operations leader of Isotope Production. Operator level will be evaluated with experience and qualifications. | 09/22/2025 |
| 484 | Reckitt Montevale, NJ R&D Assistant, Germ Protection - Lysol Aerosols BS/BA degree in a related science Exp: 0-2 years |
The R&D Assistant will work with technical product development on key projects for the R&D team. | 09/22/2025 |
| 485 | Regeneron Tarrytown, NY Associate Scientist - Formulations (Drug Product Development) BS or MS in Pharmaceutical Sciences, Biomedical Engineering, Chemical Engineering, Biochemistry, Chemistry, Biophysics or a related field Exp: 0-4 years |
Regeneron's Formulation Development Group, in Tarrytown NY is looking for an energetic Associate Scientist. In this exciting role, you support drug product development activities from candidate selection and pre-clinical development through clinical development and commercialization for a variety of drug modalities which may include mAb, ADC, siRNA, AAV, LNP in a variety of drug and delivery presentations for liquid and lyophilized DP, and novel drug delivery technologies. | 09/22/2025 |
| 486 | Regeneron Tarrytown, NY Associate Scientist - Bioassay Development BS/MS Exp: 0-2+ years |
We are seeking an experienced and motivated Associate Scientist to join the Bioassay team as a part of our Therapeutic Proteins Department. Our group’s focus is to develop assays to interrogate regulation of molecular function and signaling which contributes to the therapeutic mechanism of action and we play an integral role in discovery and characterization of therapeutic molecules across diverse disease areas. You will develop cell-based functional assays to identify and characterize therapeutic antibodies. We hope you are excited to work collaboratively across functions to meet project achievements, with the goal to deliver therapies that transform the lives of patients. | 09/22/2025 |
| 487 | Regeneron Tarrytown, NY Associate Scientist - Protein Development BS or MS in biology, molecular biology, protein chemistry, engineering chemistry, or a related field Exp: 1-3 years |
We are seeking an Associate Scientist to join Reagent group within our Therapeutic Proteins department. You will join our ongoing efforts to purify and biochemical characterize of protein reagents. | 09/22/2025 |
| 488 | Regeneron East Greenbush, NY Associate Design Quality Engineer (Medical Device) Bachelor’s degree in an Engineering subject area Exp: 0-2 years |
We are currently looking to fill a Medical Device Quality Engineer position. This position will provide Quality Assurance oversight and ensure compliance in the support of combination device development life cycles. | 09/22/2025 |
| 489 | REGENXBIO Rockville, MD Clinical Research Associate II Bachelors degree Exp: 1 year |
As a Clinical Research Associate (CRA), you will be responsible for the support and coordination of the logistical aspects of clinical trial management, site management, data review & cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs. You’ll act as a pivotal point of contact for the clinical trial team and assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. | 09/22/2025 |
| 490 | REGENXBIO Rockville, MD Clinical Research Associate (MPS) Bachelors degree Exp: 1 year |
As a Clinical Research Associate (CRA), you will be responsible for the support and coordination of the logistical aspects of clinical trial management, site management, data review & cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs. You’ll act as a pivotal point of contact for the clinical trial team and assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. | 09/22/2025 |
| 491 | Renaissance Lakewood, NJ MS&T Scientist II Master's Degree in Pharmaceutical Sciences, Formulation Chemistry, Chemical Engineering, or similar degree Exp: 1-3 years |
Perform MS&T activities with limited supervision for pharmaceutical products, including parenteral and nasal products for all new products from scale-up to commercialization and process improvement beyond commercialization. Continue to grow in understanding the overall generic and new drug development processes, Agency requirements, and CMC strategies. Understand and comply with all the Renaissance safety, environmental and quality practices and procedures as outlines in organization/departmental guidelines and SOPs, as well as applicable federal, state and local regulations. Ensure all department SOPs are in place and followed. Participate with supervision in the progress of project work with follow-ups, meeting timelines and providing appropriate technical info to the support team. Identify, develop and foster good working relationships with cross-functional teams, external customers and support initiatives required to enhance Renaissance's reputation with customers continually. This role may also be a scientific team member for client calls regarding MS&T matters. Prepare project protocols and assess and identify deliverables with limited supervision. Review technical data, documents, and proposals. Provide technical guidance with limited supervision on commercial products after launch and development products through technical communications, memos, and reports. Learn to trend data and look to continually achieve and meet specifications, providing Process Capability Analysis. Ensure batch records are written and accurate in a manner that Operations can follow them and ensure Operations are trained and feel confident in the process for commercial batches. Support any regulatory audits as assigned. Must have the ability to work in a team environment. Must comply with all company policies. Flexibility in schedule is required based on business needs. Other duties, as assigned. | 09/22/2025 |
| 492 | Resonetics Hutchinson, MN Manufacturing Engineer Bachelor’s degree in an engineering field Exp: 1 year |
Our Manufacturing Engineer focuses on introducing and establishing new Manufacturing Processes plus Process Maintenance and Continuous Improvement for existing Manufacturing Processes. Additional areas of focus may include: setup reduction, operator training, tool design or selection, performance metrics, and drafting development plans. Other daily responsibilities will include: procedure generation, participation in production readiness activities for new clients and designing continuous improvement plans for current production jobs. As improvements are identified, it will very likely be the responsibility of this individual to document, implement, train and re-qualify any changes. | 09/22/2025 |
| 493 | Restor3d Durham, NC Supply Chain Analyst Bachelor’s degree Exp: 1+ year |
The Supply Chain Analyst will be responsible for maintaining ERP data and developing analytics meet the Company’s Sales & Operations Plans and Quality Objectives. Ideal candidates will be local to Durham, NC and have experience providing supply chain data analytics and reporting for medical device manufacturers. | 09/22/2025 |
| 494 | Revolution Medicines Redwood City, CA Safety Scientist MSc in a Life sciences discipline Exp: 1+ years |
The Safety Scientist within Global Patient Safety Science is an individual contributor who provides safety science and pharmacovigilance support to all products across the RevMed portfolio, which includes early and late phase development activities. The individual will be responsible for supporting clinical studies, review of clinical trial protocols, supporting updates to IBs, ICFs, and authoring of DSURs. Additional safety related activities will involve medical review of individual case safety reports (ICSRs), safety surveillance of assigned products and active member of cross-functional teams. | 09/22/2025 |
| 495 | Revolution Medicines Redwood City, CA Clinical Trial Assistant BS or BA in relevant scientific discipline Exp: 0-3 years |
This is a unique opportunity for an entry-level Clinical Operations Professional. As a Clinical Trial Assistant (CTA), you will be responsible for providing administrative and operational support for one or more studies within a clinical program. Reporting into the Associate Director, Clinical Operations you will play a critical role in executing well-defined tasks that support clinical study start-up, maintenance, and close-out. | 09/22/2025 |
| 496 | Revolution Medicines Redwood City, CA Temp Senior Research Associate, Assay Technologies, Lead Discovery Master’s degree in biochemistry, biophysics, biotechnology, or related field Exp: 0-3 years |
We are looking for an experienced Senior Research Associate to help the Discovery Sciences team accelerate our search for new oncology therapeutics. The successful candidate will join a high-performing team of experts in the use of biochemical and biophysical screening techniques to drive the efficient identification and rapid development of clinically impactful drugs against frontier targets in oncology. Working from the bench, they will apply their biochemical and biophysical expertise. The candidate will support Discovery Science efforts to enhance how we discover inhibitors of established and new drug target proteins, as well as contribute to our mission of providing high-quality experimental data for existing programs. | 09/22/2025 |
| 497 | RION Rochester, MN Associate, Quality Control B.S. or M.S. Exp: 0-3 years |
Independently develop, validate, and oversee the performance of testing methods designed to characterize cell-based therapeutic products at various stages of product development. Perform release and stability testing on GMP and non-GMP biologic therapeutic products for both human and veterinary programs. | 09/22/2025 |
| 498 | RION Rochester, MN Research Associate, Analytical Development Bachelor's or Master's degree with focus in Biological Sciences Exp: 1+ years |
The Analytical Development Research Associate will contribute to analytical method development, implementation, and pre-qualification of methods focused on Rion’s exosome technology. This role will work closely with Rion Quality Control to execute method transfers and support continuous improvement. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, ELISA, RT-qPCR, HPLC and colorimetric/fluorometric-based assays. The Analytical Development Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Analytical Development Research Associate will work closely with the Analytical Development Scientists and support the efforts of Quality Control/Process Development. As such, the successful candidate will work in an upbeat, highly collaborative and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 09/22/2025 |
| 499 | Rivanna Medical Charlottesville, VA Product Development Engineer Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, or a related engineering discipline Exp: 1-3 years |
RIVANNA is seeking a Product Development Engineer to join our dynamic engineering team. You will work with a talented team of professionals as we strive to achieve our mission to develop and commercialize world-first imaging-based medical technologies that elevate global standards of care. As a Product Development Engineer, you will contribute to activities across the product lifecycle, from prototype development to clinical support. This hands-on multidisciplinary role involves close collaboration with the mechanical, manufacturing, and electrical engineering team on a wide range of product development tasks and projects. This job will be on-site in Charlottesville, VA; applicants must be local or willing to relocate to Charlottesville for this position. | 09/22/2025 |
| 500 | RQM+ Cary, NC Clinical Trial Associate B.S/B.A. degree in science/healthcare related field Exp: 1 year |
The Clinical Trial Associate supports the Clinical Trials team(s) in the overall management and administration of trials, including planning, execution, and closeout of one or more clinical trials in a fast-paced environment. The primary responsibility is to manage administrative tasks on behalf of the team. | 09/22/2025 |
| 501 | Sanofi Framingham, MA Manufacturing Compliance Engineer II Master's degree in sciences, Technical, Engineering Exp: 1 year |
Manufacturing Operations is responsible for supporting large scale mammalian cell culture and multi-stage large scale chromatography manufacturing operations as part of a 24/7 large-scale therapeutic protein or vaccine manufacturing facility. Operation’s main functions are leading deviation investigations and managing CAPA Implementation, partnering with direct manufacturing staff for enhancing and improving the manufacturing instruction set, overseeing and supporting manufacturing’s traini8ng program, and identifying and managing continuous improvement initiatives. Manufacturing Compliance Engineer II uses expert knowledge of compliance and GXP manufacturing processes to manage investigation and improvement initiatives within manufacturing operations. | 09/22/2025 |
| 502 | Sanofi Framingham, MA Senior Manufacturing Technician Bachelor's degree in Biotech Exp: No exp |
This is a 12 hour, rotating position in a large scale cGMP biologics facility. The Sr. Manufacturing Technician will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 09/22/2025 |
| 503 | Sanofi Pearl River, NY Production Technician USP BS degree Exp: 1-3 years |
Primary responsibility of the incumbent will be operation of general manufacturing equipment under close supervision in accordance with current relevant quality standards or standardized procedures and within safety guidelines in the production of Flublok Drug Substance in the large-scale recombinant protein production operations of the cGMP commercial manufacturing facility. Requires good documentation skills and attention to detail. Duties will include the operation, maintenance, cleaning and sanitization of large-scale cell culture bioreactors and associated operations such as media preparation, infection, and harvest. Activities will include executing techniques such as large-scale bioreactor cell expansion with the use of stainless-steel vessels and single use bioreactors (SUBs) including transfer lines, ancillary equipment (tube welders, tube sealers, peristaltic pumps), use of water-for-injection (WFI) point of use taps, etc. | 09/22/2025 |
| 504 | Sanofi Swiftwater, PA Production Technician - Vaccines Bachelor’s degree in Life Sciences or other relevant field Exp: No exp |
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. | 09/22/2025 |
| 505 | Saptalis Hauppauge, NY Quality Control Scientist BS/MS Degree (chemistry or related field) Exp: 0-2 years |
Saptalis is looking to recruit QC Scientists to join the growing Quality group at our facility in Hauppauge, NY. QC Scientist is responsible for GMP testing of raw materials, in-process, finished product and stability samples for release. In addition, the responsibilities include maintaining laboratory equipment, assisting in investigations and coordinating external testing as needed. | 09/22/2025 |
| 506 | Serán Bend, OR Scientist/Engineer, Drug Product Development Bachelor or Master’s degree in pharmaceutical science, chemistry, chemical engineering, biological engineering, mechanical engineering, materials scie Exp: 1 year |
Serán seeks to hire a Scientist/Engineer to join the Drug Product Development group and contribute as part of an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. The role requires strong hands-on laboratory skills and the ability to apply fundamental scientific principles to solve problems. Strengths in data collection, analysis, proactive communication, and continuous learning by textbooks, journals, and training will enable the successful candidate to thrive. The ideal candidate would enjoy a work environment that is both science-focused and adaptable to meet rapidly changing project needs. Preference will be given to candidates with higher experience levels. | 09/22/2025 |
| 507 | Siemens Buffalo Grove, IL Mechanical Engineer - Hardware & Devices Bachelor’s degree in mechanical engineering or another related field Exp: Entry level |
Design and develop mechanical hardware and devices Work with senior engineering personnel, mechanical engineers, lab engineers, technical writer, approvals manager, technicians, and others within the organization to coordinate development of designs. Generate development and product costs, schedule, and mechanical engineering specifications to support design team and adjacent functions. Provide support of existing products, drive Cost Value Engineering efforts, and assist in the development of new mechatronic products. Assemble or direct the assembly of mechanical hardware and systems and other tasks. Use engineering and other software for project management, engineering, development (3D modelling), and report writing. Prepare rough copy of technical documentation to support product designs. Work with outside vendors to optimize design and obtain costing for production quantities and tooling. Assist field employees in trouble shooting product problems in field offices, distributors, or customer locations. May visit suppliers to assist in resolving their production problems. Generates development and product cost, schedule, and mechanical engineering specifications to support design teams. Create models and drawings for components and assemblies using CAD software. Coordinate the design, sourcing, assembly, and testing of concept models to validate production ready designs. Initiate and execute change requests driven by new product introduction, design-to-cost efforts, supplier change etc. | 09/22/2025 |
| 508 | Siemens Wendell, NC Electro-mechanical Quality Test Technician- 2nd Shift Bachelor’s degree in electrical engineering Exp: 1+ years |
We are looking for an Electro-mechanical Quality Test Technician for our Motor Control Center (MCC) team on 2nd shift. This position will be based in Wendell, NC. The Electro-mechanical Quality Test technician is responsible for performing final test and inspection duties on Low and Medium Voltage Electrical Distribution Equipment, such as Switchgears, Switchboards and Breakers. | 09/22/2025 |
| 509 | Siemens Healthineers Newark, DE System Engineer Bachelor’s degree in Mechanical/Electrical/Chemical Engineering or related discipline Exp: 0-3 years |
Learn and apply mechanical and/or electrical process automation principles and technology to design, develop, document, install, qualify, and optimize new and upgrade existing automated medical diagnostic consumable device manufacturing equipment, batch processing systems, and semi-finished reagent formulation systems in a constantly changing fast-paced environment. Work closely with cross-functional senior design team members to develop understanding of subsystem/system functionality and performance. Supporting troubleshooting, determining root cause, and then implementing design modifications as they pertain to highly complex automated production assembly and packaging system performance. Work within small projects teams for business expansion, quality improvements or efficiency improvements to existing equipment. Execute experiments to generate and collate system performance test data to support establishing acceptance criteria. Develop technical writing skills by creating technical documentation such as validation documentation, functional specifications, user requirements, and manufacturing work instructions. Assure compliance to all design characterization, integration and verification quality procedures and policies of process development and validation. Collaborate with Senior level System Engineers, Technical Operations and Manufacturing teams. Providing routine off-hour process support for mechanical equipment issues, typically one week in every 10 to 12 weeks, or as required. | 09/22/2025 |
| 510 | Siemens Healthineers Walpole, MA Laboratory Technician BS/BA in related discipline Exp: 0-2 years |
In your activities you will execute the build of large-scale automated equipment in Walpole Formulation. You will assist in meeting product demand requirements: manufacturing product, allocating bill of materials and routings. You will assist in calibration and maintenance of lab equipment, and lab duties as required. You will work within a regulated laboratory environment: knowledge of and compliance with ISO, GMP, QSR. You will work with laboratory software: knowledge of Microsoft Office, basic understanding of SAP. You will demonstrate a basic knowledge of professional principles and skills. You will use fundamental concepts, practices, and procedures of the particular area of specialization. You will assist in fostering the team environment. Your contacts will be primarily with immediate manager and others in the group. This position includes the handling of all types of materials, including hazardous and DEA (Drug Enforcement Agency) controlled materials. | 09/22/2025 |
| 511 | Siemens Healthineers Newark, DE External Manufacturing Operations Engineer M.S. in Chemistry, Biochemistry, Engineering, Medical Technology, Biology, or a related discipline Exp: 1-3 years |
Serve as the primary liaison with OEM partners for all manufacturing-related activities involving finished products within the Laboratory Systems Business Unit. Ensure adherence to Siemens Healthineers’ Quality Management System. Familiarity with Supplier Corrective Action Reports (SCAR) and Corrective and Preventative Actions (CAPA) is highly desirable. Review and approve verification, qualification, and validation protocols and results conducted at OEM sites, particularly during the commissioning of key equipment and components for Siemens-owned, supplier-operated assets. Lead or coordinate in-house testing when necessary. Provide technical assessments for Supplier Change Notices, including changes to manufacturing processes, raw materials, in-process testing, equipment, and manufacturing locations, in collaboration with Technical Operations. Lead and coordinate escalations of OEM-initiated change notices to the Change Review Board (CRB), including associated documentation and testing. Manage the implementation of Siemens Healthineers-initiated changes at OEM sites. Manage capital and expense budgets for Siemens-owned, supplier-operated equipment. Collaborate with suppliers and Siemens finance teams to ensure assets are properly funded, maintained, and have sufficient capacity. Prepare and submit Applications for Investment (AFIs) as needed. | 09/22/2025 |
| 512 | Siemens Healthineers Palo Alto, CA Product Quality Engineer Master's degree in Engineering Exp: No exp |
Varian, a Siemens Healthineers company is seeking a dedicated and detail-oriented Product Quality Engineer to join our team in Palo Alto, California. In this position, you will play an instrumental role in engaging with our local and global partners, driving various transformation initiatives and providing daily support to our manufacturing operations. | 09/22/2025 |
| 513 | Sino Biological Houston, TX Downstream Associate Bachelor’s degree in Biology, Biochemistry, Biotechnology, or a related field Exp: 0-3 years |
This is an entry-level position suitable for individuals seeking hands-on experience in protein purification and quality control in an industrial bioprocessing environment. The Associate will support the downstream team in executing purification workflows and conducting protein characterization assays to evaluate product quality. Responsibilities include chromatography-based purification, recombinant protein QC related tasks under the guidance of project scientists. This role requires strong attention to detail, good lab documentation practices, and effective collaboration with cross-functional teams. | 09/22/2025 |
| 514 | Singota Solutions Bloomington, IN Associate QA Specialist - Quality Events Bachelor’s Degree in Science related field Exp: 1-3 years |
The Associate QA Specialist - Quality Events position is responsible for supporting and maintaining the GMP-compliant quality systems related to deviations and CAPAs (Corrective Action & Preventative Action). This role provides quality oversight of quality event lifecycle management, ensures adherence to internal procedures and regulatory requirements, and interfaces directly with internal teams, external clients, and regulatory bodies. This position plays a key role in maintaining site compliance and driving continuous improvement across operations. | 09/22/2025 |
| 515 | Revvity Hebron, KY Associate Quality Assurance Engineer Bachelor’s degree Exp: 0-2+ years |
This position supports the review of client records for any HCT/P that is sent for clinical trial participation, transplant, or research and review of batch records for contract processing. This role supports the day-to-day needs of the company regarding change management and controlled documents. This role is also involved in various initiatives within the Quality department, which includes the overall processes of the maintenance and archival of records. Supporting internal quality activities that relate to the overall operation of the site’s quality program. | 09/22/2025 |
| 516 | Revvity San Diego, CA Research Associate II - Cell Analysis Bachelor’s Degree in life sciences or other relevant field Exp: 1+ years |
At BioLegend (a Revvity, Inc. company) we develop novel, cutting edge products and offer custom services to help with scientific innovation and discovery. We are currently looking for a talented, detail oriented person to join our growing Product Development team. The potential candidate will assist with development of new products for cell analysis such as antibodies, multi-color panels, and reagents for analysis of cell metabolism and cell imaging. The successful candidate must be a self-motivated, team player, able to communicate effectively with a multi-disciplinary team and must possess excellent organization skills. | 09/22/2025 |
| 517 | SK Pharmteco Rancho Cordova, CA Quality Chemist I Bachelors degree Chemistry, Microbiology or Related Field Exp: 0-1 years |
The Quality Control Chemist I will be responsible for analyzing and making determinations as to the quality of a product, using analytical equipment pertinent to the appropriate application of skills. This position provides solutions to a variety of technical problems of moderate scope and complexity. Work is closely supervised. | 09/22/2025 |
| 518 | Sofie Totowa, NJ Environmental Monitoring Technician Bachelor’s Degree in a Life Science discipline Exp: 0-3 years |
The Microbiology - Environmental Monitoring Technician supports microbiology and manufacturing activities at the NJ5 site by (1) performing Environmental Monitoring (EM) as per sampling schedules (2) detecting, quantifying, identifying, and aiding in investigations for possible contaminants that may impact the quality of product during different stages of the manufacturing process. | 09/22/2025 |
| 519 | Sovereign Pharmaceuticals Fort Worth, TX QC Lab Technician BS Related scientific field Exp: 1-2 years |
The primary function of a QC Laboratory Technician is to perform the following duties: Sample receipt (logging and labeling) of all samples into the lab, verifying documentation, DEA forms, etc., and entering into Excel to aid laboratory scheduling by supervision. Ordering reagents/standards/office supplies and submitting to purchasing. Glassware cleaning. Solution/standard preparation. DEA reconciliation of completed samples. Receiving reagents/consumables. Inventory management (full inventory of reagents in the lab each week). Receiving and tracking reference standards. General house-keeping such as stocking consumables. Destruction of completed noncontrolled samples. Assist with Stability Program management (sample placement/retrieval from the chambers). Assist with retaining sample storage/retrieval | 09/22/2025 |
| 520 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist I BA/BS Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 09/22/2025 |
| 521 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist II BA/BS Chemistry Exp: 1 year |
The primary function of a QC Chemist II is to perform to a high level in qualitative and quantitative chemical and physical analysis in support of two of the following areas: Analysis of raw materials and packaging components. Analysis of in-process and finished drug products (including stability) of primarily high-volume products. Analysis of high potency products | 09/22/2025 |
| 522 | Genentech South San Francisco, CA Bioprocess Technician - Clinical Supply Center Bachelor Degree Exp: 1-3 years |
The Clinical Supply Center Bioprocess Technician is an integral member of the Clinical Supply Center (CSC) team in South San Francisco (SSF). The SSF CSC is a state-of-the-art large molecule drug substance facility which supports GMP production for phase 1, 2 and early phase 3 clinical trials. The CSC employs a ballroom design, utilizing single-use technology, new analytical techniques and digital manufacturing systems to deliver a best in class bioprocess facility. We are looking for individuals to support this facility who are comfortable with ambiguity, have an entrepreneurial spirit within a GMP environment, have demonstrated strong Pharma Technical Behaviors, and have an agile mindset. Ability to collaborate is crucial as success will be measured as a member of a team, not just as an individual. Ideal candidates would have experience in a broad range of functional roles in support of biopharmaceutical production. | 09/22/2025 |
| 523 | Penumbra Alameda, CA Manufacturing Engineer I, Operations Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing and business processes with interaction between production, cross-departmental engineering groups, and other cross-functional teams (such as Regulatory, Quality, R&D, Supply Chain, IT, etc.) in executing and coordinating business operations systems projects and activities. Essential job functions include creating and executing an integrated cross-functional project plan. | 09/15/2025 |
| 524 | Penumbra Alameda, CA Manufacturing Engineer II, Operations Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing and business processes with interaction between production, cross-departmental engineering groups, and other cross-functional teams (such as Regulatory, Quality, R&D, Supply Chain, IT, etc.) in executing and coordinating business operations systems projects and activities. Essential job functions include creating and executing an integrated cross-functional project plan. | 09/15/2025 |
| 525 | Pfizer Andover, MA Process Engineer II Bachelor's degree Exp: 0+ years |
Execute production activities using knowledge of process equipment, systems, and manufacturing operations. Participate in operational qualification training and assist the Team Lead as needed. Ensure all activities comply with Company policies, standard operating procedures, Pfizer Values, and global regulatory and environmental guidelines. Work in a structured environment using established procedures. Ensure work is regularly reviewed for technical judgment, completeness, and accuracy. Assist in troubleshooting, technology transfer, and start-up activities. Oversee technical documentation for production and process approvals, ensuring compliance with Current Good Manufacturing Practices, and manage process activities by adhering to Standard Operating Procedures. | 09/15/2025 |
| 526 | Pfizer Groton, CT Quality Operations Drug Product: Associate Bachelor's degree Exp: 0+ years |
This Quality Operations (OQ) position will support the Groton, CT PharmSci Small Molecules QO department by assisting in quality operations activities related to the manufacture and disposition of GMP clinical Drug Product. As an Associate Operations Quality colleague, the successful candidate will have quality touchpoints prior to the start of drug product manufacturing through disposition of final drug products for clinical use. Paramount to this role will be acting as a quality point of contact for supporting investigations and ensuring compliance with regulatory and internal standards. | 09/15/2025 |
| 527 | Pfizer Rocky Mount, NC Senior Automation Engineer Master's degree Exp: 0+ years |
As a Sr. Automation Engineer your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate explaining difficult issues and establishing consensus between teams. | 09/15/2025 |
| 528 | Pfizer Rocky Mount, NC Automation Engineer Bachelor's degree Exp: 0+ years |
As an Automation Engineer your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. | 09/15/2025 |
| 529 | Pfizer Groton, CT In Vivo Technician Specialist, Drug Safety R&D Bachelor of Science degree, Biological Sciences (or equivalent) Exp: 0-2 years |
The In Vivo Technician role functions within study execution and provides non-Good Laboratory Practice (GLP) and GLP in vivo study conduct expertise to advance the Pfizer portfolio, particularly for the selection of new therapeutic candidates but also for support of later stages of clinical development and registration. The In Vivo Technician is responsible for performing accurate, high quality in-life study work for rodent and non-rodent safety studies in compliance with the study protocol, Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP) regulations, Environmental Health and Safety (EHS) standards, animal welfare regulations, and departmental policies/procedures. The data collected on these studies by the In Vivo Technicia | 09/15/2025 |
| 530 | Pharmaron Exton, PA Associate Scientist, In Vivo PK Bachelor of Science (Biology, Biochemistry, Pharmaceutical Life Sciences) Exp: 1 year |
The Associate Scientist will play an integral role in growing the operations and customer base by supporting the analysis of various samples and performing studies/assays independently while delivering exceptional quality with a high attention-to-detail and ensuring client expectations are met. | 09/15/2025 |
| 531 | Pharmaron Exton, PA GMP QC Analyst I Bachelor's or Master's degree Exp: 0-3 years |
We are seeking a highly motivated GMP QC Analyst I/ II to join our Cell & Gene Therapy (CGT) Quality Control team. The QC Analyst I/ II will be responsible for executing routine laboratory testing under cGMP conditions to support multiple client projects in various phases of development. This role is suitable for candidates seeking to gain hands-on experience in a dynamic, client-focused, cross-functional CGT laboratory. The ideal candidate will have a strong foundation in biological sciences and laboratory techniques, along with a commitment to quality and regulatory compliance. | 09/15/2025 |
| 532 | Pharmaron Exton, PA GMP QC Analyst II Master's degree Exp: 1-3 years |
We are seeking a highly motivated GMP QC Analyst I/ II to join our Cell & Gene Therapy (CGT) Quality Control team. The QC Analyst I/ II will be responsible for executing routine laboratory testing under cGMP conditions to support multiple client projects in various phases of development. This role is suitable for candidates seeking to gain hands-on experience in a dynamic, client-focused, cross-functional CGT laboratory. The ideal candidate will have a strong foundation in biological sciences and laboratory techniques, along with a commitment to quality and regulatory compliance. | 09/15/2025 |
| 533 | Pharmaron Exton, PA Quality Control Associate Bachelor's degree in pharmaceutical sciences, life sciences or a related scientific field Exp: 1+ years |
The Quality Control Associate will be responsible for review and drafting of data and reports generated in support of DMPK and CGT studies at Pharmaron US lab Services. | 09/15/2025 |
| 534 | Quest Diagnostics Cleveland, OH Bio-Analytical Instrument Technician BA/ BS degree or above (preferably in science, engineering, or computer information) Exp: 1-2 years |
Provides assistance to internal clients and is accountable for working independently with minimal supervision. The position requires strong communication skills both verbal and written plus technical skills to accomplish job responsibilities. | 09/15/2025 |
| 535 | Quest Diagnostics Lenexa, KS Forensic Toxicology Laboratory Scientist I Bachelor’s Degreee Exp: 1 year |
This position works within the Forensic Toxicology Laboratory and is responsible for all aspects of testing of donor specimens including specimen preparation and instrument operation. | 09/15/2025 |
| 536 | Quest Diagnostics San Juan Capistrano, CA Bio-Analytical Instrument Technician BA/ BS degree or above (preferably in science, engineering, or computer information) Exp: 1-2 years |
Provides assistance to internal clients and is accountable for working independently with minimal supervision. The position requires strong communication skills both verbal and written plus technical skills to accomplish job responsibilities. | 09/15/2025 |
| 537 | Quest Diagnostics Shelton, CT Cytogenetics Technician I Bachelor of Science (Biology or Chemistry Preferred) Exp: 1 year |
Perform various routine laboratory functions in a precise and accurate fashion to assist the laboratory professional staff and to facilitate production. | 09/15/2025 |
| 538 | Quest Diagnostics Greensburg, IN Medical Laboratory Scientist I Generalist BS/BA in Chemistry or Biology Exp: 1 year |
Are you intrigued by the science of the human body? Curious about state-of-the-art laboratory instrumentation? Looking to join a Fortune 500 company leading the world in providing diagnostic information services? Quest Diagnostics is now recruiting for technologist positions ranging from entry level to experienced, with a wide range of benefits and training! | 09/15/2025 |
| 539 | Quest Diagnostics Kokomo, IN Medical Laboratory Scientist I Generalist BS/BA in Chemistry or Biology Exp: 1 year |
Are you intrigued by the science of the human body? Curious about state-of-the-art laboratory instrumentation? Looking to join a Fortune 500 company leading the world in providing diagnostic information services? Quest Diagnostics is now recruiting for technologist positions ranging from entry level to experienced, with a wide range of benefits and training! | 09/15/2025 |
| 540 | Phlow Richmond, VA Scientist, Engineering BS or MS in Chemical engineering Exp: 0-5 years |
The purpose of this role is to provide engineering support to Phlow’s Manufacturing Science and Technology (MS&T) group. This is an exciting opportunity for recent graduates or individuals with process engineering experience to independently design, install, and operate continuous and batch processing equipment under the direction of a Principal Scientist or other team member. The candidate will provide engineering support to the MS&T group including equipment selection and design, heat and mass transfer calculations, and scale-up modelling. The candidate will support execution Phlow’s internal API development projects as well as the CDMO business to ensure business objectives are met. The candidate will ensure excellence of our process development and technical transfer to Phlow’s partners or customers. The candidate will personify Phlow’s shared values and culture, both internally and externally. The candidate will work with the highest standards of safety, integrity, transparency, and ethics to create win-win scenarios for patients, customers, partners, and colleagues. | 09/15/2025 |
| 541 | Phlow Richmond, VA Laboratory Assistant B.S degree in Chemistry, or related scientific field Exp: 1+ years |
This role contributes to Phlow's mission by supporting laboratory work related to analytical chemistry and process development. The position involves performing laboratory operations activities in Phlow’s R&D laboratories located in Richmond and Petersburg, under the guidance of the Senior Director, Analytical Chemistry, or other team members. This position is a full-time, day shift position, Monday-Friday. The expected schedule will involve rotating days during the week between the Petersburg and Richmond locations. The team member plays a critical role in ensuring Phlow’s ability to conduct contract development and manufacturing services and the successful execution of both internal API development projects and commercial initiatives. Responsibilities include safety and housekeeping, inventory and procurement of supplies, equipment maintenance or calibration, collaborating with scientists to meet business objectives and timelines, and upholding Phlow’s shared values and culture in all interactions, both internally and externally. This role requires maintaining the highest standards of safety, integrity, transparency, and ethics in all aspects of work. By doing so, the team member contributes to delivering outcomes that create win-win scenarios for patients, customers, partners, and colleagues while fostering an innovative and collaborative environment at Phlow. | 09/15/2025 |
| 542 | Pledge Therapeutics Canton, MA Research Associate, Immuno-Oncology MS Exp: 1-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our new state-of-the-art facility in Canton, MA. The successful candidate will engage in the Immuno Oncology research areas of the company and will work with a successful team of international senior scientists located in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 09/15/2025 |
| 543 | Pledge Therapeutics Canton, MA Research Associate, Virology Bachelor’s or Master’s degree in biological sciences or a related field Exp: 0-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our state-of-the-art facility in Canton, MA. The successful candidate will engage in the company’s virology research areas and work with a successful team of scientists in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 09/15/2025 |
| 544 | PolyPeptide San Diego, CA QC Chemist BS degree in Chemistry or Biochemistry or equivalent Exp: 1+ years |
The Quality Control Chemist performs analytical testing on raw materials, intermediates, and finished peptide products using a range of laboratory instruments to ensure compliance with quality standards and GMP guidelines. This role prepares samples, calibrates equipment, documents results, and identifies potential quality issues, supporting the development of corrective actions as needed. The chemist also contributes to SOP development and maintains a clean, compliant laboratory environment. This role contributes directly to PolyPeptide’s commitment to delivering exceptional quality and on-time delivery to our customers. | 09/15/2025 |
| 545 | Precigen Germantown, MD GMP Gene Therapy Manufacturing Associate Bachelor’s degree or Master’s degree in biology, biomedical science, or life science Exp: 1-3 years |
We are seeking a hard-working GMP Gene Manufacturing Associate I/II (level determined by candidate experience) at our Germantown, MD location to join us in our mission to serve patients with our next generation of innovative Gene Therapies. This position will require a professional who thrives in a dynamic team environment, brings meticulous attention to detail in the quality of their work and is proactive in implementing improvements. This position will perform a broad range of tasks in the cGMP manufacturing of clinical and commercial adenovector products. Prior experience in GMP manufacturing and operation of GMP process equipment are required. | 09/15/2025 |
| 546 | Proclinical Wilmington, DE Staff Scientist, ADME Bachelor's degree in biology, Life Science, or related discipline. Exp: 0-3 years |
Proclinical is working alongside a pharamceutical company seeking a Staff Scientist to join the team. The Staff Scientist, DMB is primarily responsible for DMPK support of discovery and/or development projects regarding in vivo pharmacokinetics studies. The successful candidate will involve preparing doses for, scheduling, and coordinating in vivo pharmacokinetics studies as well as generic lab functions with the opportunity for cross training on in vitro assay support. | 09/15/2025 |
| 547 | Proclinical Wilmington, DE Chemical Library Inventory Specialist BS (or equivalent laboratory experience) in Chemistry/Life Sciences or related field Exp: 0-5 years |
We are seeking a motivated and scientifically curious chemical library specialist to join our client's Discovery Chemistry department and contribute to the development of internal high-throughput screening chemical library. This role offers an exciting opportunity to apply chemistry knowledge towards the discovery of new therapeutic entity. | 09/15/2025 |
| 548 | ProMed Plymouth, MN Manufacturing Engineer 2-Metrology Focus Bachelor's degree in mechanical, quality, or manufacturing engineering Exp: 1 year |
We're seeking a Manufacturing Engineer II with Metrology Focus to join our Manufacturing Operations team. This is an important role that safeguards product integrity and regulatory compliance through advanced metrology systems and precision measurement protocols that directly impact patient safety and market access. We are seeking a Manufacturing Engineer II with Metrology Focus to join our Operations Engineering team at ProMed Molded Products. You'll design and implement metrology systems that ensure dimensional accuracy across manufacturing processes while developing quality assurance procedures that detect non-conformances before product release. Your expertise will establish measurement uncertainty analysis and gauge repeatability studies, validating system capability for reliable quality data. You'll create process validation protocols and documentation systems supporting regulatory submissions, while designing manufacturing work instructions that ensure consistent execution and reduce operator variability in our medical device manufacturing environment. We're only considering candidates from The Minneapolis Metro area. No relocation assistance is available for this role. | 09/15/2025 |
| 549 | PSC York, PA QC Analyst I Bachelor’s degree in related science discipline, i.e. Chemistry, Microbiology Exp: 1-3 years |
We are hiring an entry-junior level QC Analyst I. The QC Analyst I will be responsible for conducting quality control testing in the and ensuring the safety, efficacy, and consistency of products. This role involves rigorous analysis at every stage to ensure compliance with regulatory standards and internal quality guidelines. | 09/15/2025 |
| 550 | PSC San Francisco, CA Commissioning Engineer Bachelor’s degree in engineering or a related technical discipline Exp: 1-3+ years |
We are hiring an experienced Commissioning Engineer to provide comprehensive Commissioning Services for Facilities Capital Projects. In this role, you will be responsible for ensuring the successful commissioning of systems and equipment, from design through to post-handover. You will oversee and coordinate all commissioning activities to ensure systems are properly tested, validated, and ready for operational use, in line with project specifications and industry standards. | 09/15/2025 |
| 551 | Psomagen Rockville, MD Junior Bioinformatics Scientist Bachelor’s or Master’s degree in Biology, Bioinformatics, Computer science, or similar degree Exp: 1-3 years |
Do you want to apply your talent and expertise in making a difference by helping scientists answer important questions related to human health and treating diseases? If so, Psomagen is the right place for you. We are a leading company in the genomics field, based in the U.S., seeking a skilled and motivated Bioinformatician to join our Department of Bioinformatics. This role involves managing operation systems, NGS data QC and analysis, and collaboration with the teams. | 09/15/2025 |
| 552 | Psomagen Rockville, MD NGS Laboratory Technician/Scientist/Manager Bachelor’s degree in biology or relevant major Exp: 1 year |
Psomagen Inc. is a leading multi-omics service provider specialized in NGS, Sanger, single cell sequencing services to support life science research and industry field in North America. The NGS clinical laboratory technologist will perform day-to-day NGS experiments including sample preparation, library preparation, QC procedure as well as various NGS instrument operations. | 09/15/2025 |
| 553 | Purdue Pharma Wilson, NC Quality Specialist I, Chemist BA or BS degree in Chemistry or closely related science Exp: 6 months - 2 years |
The Quality Specialist I, Chemist is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing and GMP review in support of the analysis of raw materials, packaging components, ancillary solutions, in-process samples, finished product method development and/or transfers, cleaning/process validations, and stability samples. Will follow standard procedures in accordance with cGMP, GLP, DEA and company policies and procedures. | 09/15/2025 |
| 554 | QIAGEN Germantown, MD Senior Technical Associate Bachelors degree Exp: 0-2 years |
The Senior Technical Associate, Production Molecular Biology must comprehend and perform scheduled routine bulk formulation production tasks according to established procedures in compliance with applicable regulations, including troubleshooting with assistance. | 09/15/2025 |
| 555 | QIAGEN Frederick, MD Contract Quality Assurance Associate Bachelor of Science degree in biology, chemistry, or related field Exp: 1-2 years |
The Contract Quality Assurance Associate supports operations with the implementation and maintenance of new products, procedure development, and validation. This position conducts inspection/release of manufactured product. S/he is a self-starter with strong work ethics, organizational skills, communication skills, critical thinking, attention to detail and accuracy, as well as the ability to work independently and in a team environment is essential. | 09/15/2025 |
| 556 | Quality Agents Various Locations, MA Quality Assurance Specialist BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Quality Assurance Specialists are leading service providers to our clients providing GMP support. The individual will coordinate validation activities with the client and meet timelines. | 09/15/2025 |
| 557 | QuidelOrtho San Diego, CA Development Associate 1 BS/BA or equivalent in Life Sciences or Chemistry Exp: 1-3 years |
At QuidelOrtho, we are seeking a Development Associate 1 to participate in activities to support research and new product development. The position performs simple experiments as directed by Scientist or Manager. This position will be onsite at our Summers Ridge location in San Diego, CA. | 09/15/2025 |
| 558 | QuidelOrtho Athens, OH Clinical Trials Associate BS/BA in any biological science or Medical Technologist degree Exp: 1-2 years |
As we continue to thrive together QuidelOrtho is seeking a Clinical Trials Associate to support in all clinical team activities for start-up, oversight, and study closure to include coordinating the preparation and assembly of clinical trial supplies and materials for distribution to clinical sites with minimal/moderate supervision. Maintain related tracking information of all clinical materials, shipments, and inventory. Assist the Data Management team in tracking and management of Case Report Forms (CRFs) and Laboratory submission Forms (LSFs). Assist in maintaining files and tracking of all written and electronic documentation for all study records and site interactions in the Trial Master File (TMF). Communicate with sites regarding query resolution to ensure compliance with specified protocols and accuracy of submitted data. Participate in data entry, data auditing, clinical site queries and overall clinical data flow from multiple clinical sites in a timely and professional manner. Coordinate in-house specimen procurement studies. Willingness and ability to learn, understand and apply regulatory guidelines and Good Clinical Practices (GCP’s) applicable to IVD and Medical Devices for conducting clinical field trials, CLIA Waiver and 510(k) submission studies. Be familiar with GCP, FDA regulations and relevant Standard Operating Procedures for clinical research. Develop skill and knowledge with regulatory procedures and become familiar with Quidel product development procedures. Interact with study coordinators and in-house study participants. | 09/15/2025 |
| 559 | QuidelOrtho Rochester, NY Manufacturing Shift Engineer I BS in Engineering (BSME, BSEE or BET is preferred) Exp: 0-2 years |
As the company continues to grow, as one QuidelOrtho we are seeking a Manufacturing Shift Engineer I to work in our Assay manufacturing facility. The Manufacturing Shift Engineer I is an integral member of the Assay Manufacturing Engineering team. This position will support a 24x7 high speed automated manufacturing operation and the associated engineering and maintenance functions when required to troubleshoot high level issues when impacting production. The ability to thrive in a cross-functional collaborative environment is a must. Additionally, the Manufacturing Shift Engineer shall focus on process and equipment improvements with a goal to increase overall equipment effectiveness (OEE). This position is in Rochester, NY. This individual will be working 12 hour shifts and will rotate between day and night shifts. Shift schedule is eligible for shift differential pay. | 09/15/2025 |
| 560 | QuidelOrtho Rochester, NY Engineer II BSc in Engineering or related scientific discipline. Biomedical, Chemical, Mechanical, or Systems Engineering Exp: 1-3 years |
As we continue to grow, we are seeking an Engineer II to join our R&D Field Triage group. This individual will assist in conducting technically challenging investigations to address on-market product quality issues and recommend solutions. This role involves working in a highly collaborative team setting to provide R&D investigational support including design, execution and documentation of experiments to systematically identify failure mode/s and establish root cause/s with clinical laboratory and transfusion medicine products. This position is on-site at our Rochester, NY facility. | 09/15/2025 |
| 561 | Quotient Sciences Philadelphia, PA Staff Formulator Master’s degree in Pharmaceutical Science, Chemical Engineering, or a related field Exp: 1-2 years |
Are you passionate about pharmaceutical science and ready to make a real impact in a fast-paced, collaborative environment? We’re looking for a talented and driven individual to join our team and help bring cutting-edge oral solid dosage forms to life for clinical trials across Phases I–III. | 09/15/2025 |
| 562 | Quva Bloomsbury, NJ QC Laboratory Technician Bachelor’s Degree in life science or related field Exp: 1-2 years |
Our QC Laboratory Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing basic laboratory support functions related to the management of laboratory samples, materials, and testing supplies. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. | 09/15/2025 |
| 563 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone with expertise in classifying diseases/conditions by medical specialty to do drug pipeline confirmation tasks. Contract work on a task basis. Must be able to accept payment by PayPal or Venmo. Also must be able to function in the world without using ChatGPT, because if we thought AI could do the task well, you would not be reading this job posting. Please send a message through the contact form if interested. | 09/07/2025 |
| 564 | Lilly Indianapolis, IN Automation Engineer, Drug Substance - Design & Delivery Bachelor of Science Degree in engineering or a related science field Exp: 1 year |
The Engineer – Automation - Drug Substance Design / Delivery role requires a 4-year engineering degree, preferably in Chemical, Mechanical, Electrical Engineering, or related science field. The position requires high learning agility and a background in DCS programming (preferably DeltaV) and experience in automated API manufacturing or related processes. This role will initially be in support of the design and delivery phase of the project, as part of the Global Process Automation & Control Engineering (GPACE) team. As the site nears completion and start-up activities begin, this role will transition into a Lebanon Site role for long term operational support. GPACE is part of Lilly’s Corporate Engineering Tech Center (ETC). GPACE provides automation, measurement, and process control solutions, and is a technical resource for training, standards, capital project delivery, and Lilly’s standard automation platforms. GPACE’s primary customers are global manufacturing and development sites, Manufacturing Information Technology, and peer groups such as Global Facilities Delivery (GFD). | 09/08/2025 |
| 565 | Lilly Indianapolis, IN Engineer – Automation/Process - Serialization Bachelor’s degree in Engineering Exp: 1+ years |
The Engineer - Automation/Process Serialization is accountable for the direct support throughout the design, build, site integration and verification for the new Packaging lines delivered in all Lilly Sites following GSP (Global Serialization Program) processes and procedures. Your role will involve collaborating closely with the Engineering and IT teams (Global and site). | 09/08/2025 |
| 566 | Lilly Indianapolis, IN Environmental Scientist BS or MS Degree in Environmental Sciences, Biology, Chemistry or a relevant field Exp: 0-1+ years |
The Environmental Risk Assessment Group is responsible for preparing environmental risk assessments (ERAs) to support regulatory submissions and environmental stewardship goals. The ERA group outsources studies to determine the physical chemical properties, environmental toxicity, and environmental fate of Lilly active ingredients and related chemicals. Members of the ERA group support issues related to pharmaceuticals in the environment (PiE) and advance the science of environmental risk assessment (ERA). The ERA group is part of the Health Safety and Environment (HSE) function of Lilly Research Laboratories. The ERA group is seeking an enthusiastic, well-organized and detail-oriented individual to manage study contracting, projects, scientific data and documents. The individual will need a science degree in order to understand, review and extract data from technical documents. The individual should enjoy using innovative methods to analyze and improve processes. | 09/08/2025 |
| 567 | Novartis Morris Plains, NJ Cell Processing Specialist I Bachelor’s degree in relevant Engineering or Scientific discipline Exp: 1 year |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. The CPS I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 09/08/2025 |
| 568 | Novartis Cambridge, MA Research Scientist II, Biologics Engineering and Bioconjugation Bachelors or Masters degree in biochemistry, molecular biology or related Exp: 1 year |
We are seeking a highly motivated and creative scientist to join the Biologics Engineering and Bioconjugation (BEC) unit within BRC at Cambridge site. The BEC unit drives a diverse portfolio of biologics drug discovery programs that cover various biologics modalities, such as multi-specific antibodies, non-antibody proteins, ADC and AOC therapies through knowledge-based and structure-based rational design. In this role, you will have the opportunity to learn new and cutting-edge technologies and grow your career in Novartis and in the pharmaceutical industry. This role will help to advance our diverse programs in BRC biologics pipeline and accelerate the discovery process. This associate will mainly work in the lab to support all projects cross the portfolio in the protein engineering function by contributing to protein expression, purification, characterization, and constructs design. | 09/08/2025 |
| 569 | Novartis Indianapolis, IN Maintenance Technician Bachelor's Degree Exp: 1+ years |
The Maintenance Technician is responsible for performing corrective and preventative maintenance and support services for the building(s) and all equipment for a GMP Radioligand Therapies Production Facility. Responsible for reliable, efficient, and sustained operation of the facility and all equipment. Additionally supports current project operations and site goal objectives and ensures compliance with regulatory, corporate, and site requirements related to their functional area. | 09/08/2025 |
| 570 | Novartis Morris Plains, NJ Manufacturing Operations Specialist Bachelor’s degree in a relevant scientific discipline Exp: 1 year |
This role is responsible for working with the Manufacturing Operations team to complete all daily responsibilities for manufacturing support as well as aiding the oversight of all activities occurring in the manufacturing (Shopfloor) area on the 3rd shift to ensure quality and compliance, high performance and scheduled delivery. | 09/08/2025 |
| 571 | Novartis Indianapolis, IN HSE Technician, Isotopes Manufacturing Bachelor’s degree in industrial hygiene, health and safety, engineering, or related field Exp: 0-2 years |
The HSE Technician will be responsible for supporting all HSE compliance aspects at our new state-of-the-art Isotope Manufacturing site. You will help ensure Health, Safety and Environmental activities are managed according to applicable laws and Novartis HSE Management System requirements and assist in the continuous improvement of applicable HSE Management Systems while helping to spread our safety and environmental culture by proactively engaging associates and enhancing awareness. | 09/08/2025 |
| 572 | Novartis East Hanover, NJ Clinical Lab Techician - Scien. Support BA in cell biology, immunology, molecular biology, virology, biochemistry, microbiology, or other related science Exp: 0-5 years |
Under general direction, perform supporting and administrative activities supporting the Raw Materials, BioAnalytics and Microbiology in the Analytical Operations department of TRD CGT East Hanover. | 09/08/2025 |
| 573 | MP Biomedicals Solon, OH Life Science Lab Technician Bachelor of Science in Biochemistry/Chemistry/Biology Exp: 0-3 years |
The Life Science Lab Technician (Technical Manufacturing) performs a wide variety of routine production tasks in Technical Manufacturing and must be capable of producing large-scale components for MP Bio life science products. The Lab Technician must be capable of following work instructions and finish assigned tasks on time. The ideal candidate will have a strong background in Chemistry, Biochemistry, and Biology, attention to detail, time management skills, and the ability to work effectively in a team environment. | 09/08/2025 |
| 574 | NAMSA Atlanta, GA Microbiology Technologist Bachelor degree Exp: No exp |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform required specific testing as applicable. May be required to operate specified laboratory equipment. May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable). Other duties as assigned | 09/08/2025 |
| 575 | NAMSA Minneapolis, MN Lab Technologist - In Vitro Bachelor’s degree in biology or related scientific field Exp: 1 year |
Executes routine testing per NAMSA SOPs, with appropriate data analysis (cytotoxicity and hemocompatibility). Strictly adheres to GLP guidelines (good documentation, labeling and expiration of materials, participation in audits). Performs maintenance of cell lines through propagation, cell concentration and viability determination, and creation of plates used for standard testing. Performs the extraction process on prepared samples in accordance to ISO, USP and/or JMHLW regulations as directed by study protocol for biocompatibility assays. Communicates with external clients in regards to particulate observations or article abnormality. Routinely communicates with Study Directors and Quality Assurance about issues, results, or audits. Operates, cleans and maintains incubators, autoclaves, hoods, and other equipment routinely utilized. Performs preparation of media/reagents, maintains reagents and/or test article as required for testing, and maintains lab supplies/inventory. Performs data entry, routine calculations, analysis and interpretation of results, and routes all positive results or unusual testing occurrences to Management and/or the Study Director. Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and taking all concerns to management or Study Directors as required. May assist Associates with performing routine test article/product preparation according to work instructions. May communicate test schedule updates to NAMSA Associates or management as needed. Maintains ancillary records (logbooks, worksheets). May be required to perform personal gowning, environmental testing, and submitting organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing. Adheres to established company processes. May provide administrative support. May prepare and maintain sterile glassware for the In-vitro lab and sample preparation process. Processes glassware through washer, autoclave and depyrogenation oven as needed. Completes chain of custody documentation for test article tracking. Responsible for daily monitoring of laboratory equipment, being on-call and responding to continuous monitoring alarms. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May assist in ordering and/or stocking supplies subject to approval. May assist trainers or may become a certified tra | 09/08/2025 |
| 576 | Natera San Carlos, CA Clinical Lab Associate I BS/BA in a biological science or similar field of study Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. Schedule is Mon-Fri, from 830am-5pm. | 09/08/2025 |
| 577 | Natera Austin, TX Clinical Lab Operator I BS/BA in a biological science or a related field Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. | 09/08/2025 |
| 578 | Natera Austin, TX Process Associate 1 Bachelors in Molecular Biology, Biochemistry, Molecular Genetics, or equivalent Exp: 0-2 years |
The Process Associate I (PA-I) within the Process Development - Reagents team (PDO-RGT) works under the guidance of the Reagents QC Development Manager and collaboratively with Scientists within the team to modify existing methods and/or develop and optimize new QC methods to support routine lot release of reagents and kits used in the CLIA laboratory for molecular and genetic based tests. The Process Associate works hands on at the bench to carry out experiments and studies to support bio-chemical verification and validation efforts. The PA-I also supports investigation efforts required for resolving reagent preparation and qualification issues that arise for the CLIA lab. The PA-I works hands-on to carry out experiments and studies with moderate guidance to support process improvement and technical transfer efforts. | 09/08/2025 |
| 579 | NeoGenomics Aliso Viejo, CA Laboratory Technician I - Flow Cytometry, Overnights BS or BA degree is required (in a life or physical science field is strongly preferred) Exp: 1+ years |
Under the direct supervision of licensed personnel, or within a training environment, the Laboratory Technician will assist with responsibilities associated with processing specimens for clinical testing and will provide general support for the laboratory following established policies and procedures. This is the entry level for the Laboratory Technician job category. The employee works in a learning capacity while performing a range of laboratory technician assignments under close supervision. | 09/08/2025 |
| 580 | Neuralink Austin, TX Surgery Mechanical Engineer Bachelor's or Master's Degree in Mechanical Engineering or equivalent Exp: 1-10 years |
The Surgery Engineering team is responsible for developing and managing custom hardware and processes for neurosurgical procedures, excluding the R1 Robot and Operator Station. Their responsibilities encompass the entire surgical process, including patient positioning, incision, craniectomy, precise implant placement, robotic thread insertion success, surgical site irrigation, implant installation, and closure. Additionally, the team ensures safe explantation and upgrade procedures for implants. They also provide mechanical engineering support to the animal care, histology, and BCI teams, contributing to the success of complex neurosurgical procedures and related research activities. | 09/08/2025 |
| 581 | Neuralink Austin, TX Quality Assurance Specialist Bachelor of Science degree, preferably in a science, engineering, or quality-related discipline Exp: 1 year |
The Quality Assurance (QA) Specialist will work with Neuralink's teams to ensure that the appropriate governing body regulations are followed. This includes, but is not limited to, adherence to ISO standards, Good Laboratory Practices (GLP), clinical guidelines, manufacturing protocols, and quality control practices. | 09/08/2025 |
| 582 | Neurona Therapeutics South San Francisco, CA Preclinical Research Associate Bachelor’s degree Exp: 1-2 years |
Our ideal candidates are self-motivated individuals who have clearly demonstrated a passion for scientific research. This is a fantastic opportunity to join a small team, work on transformative science, and build an exciting, science-driven company. Neurona is proud to be an equal opportunity employer and will consider all qualified applicants for employment. | 09/08/2025 |
| 583 | Noah Medical San Jose, CA Manufacturing System Technician BS in Computer Science, Electrical Engineering, or Industrial Engineering Exp: 1 year |
We are seeking a skilled Test Technician to join our team. The ideal candidate will be responsible for testing and troubleshooting medical robotic systems while adhering to Good Manufacturing Practices (GMP). The successful candidate will have a strong understanding of robotic hardware, sensors, motors, PLC’s, relays, circuit boards, computers, cabling and experience with and testing, excellent troubleshooting skills, and GMP experience. | 09/08/2025 |
| 584 | Aptar Pharma Congers, NY Quality Engineer Bachelor’s Degree Exp: 1-5 years |
The Quality Engineer (QE) is primarily responsible for the design and execution of qualification & validation activities, leading the implementation of new or modification of existing manufacturing equipment/processes (e.g. Injection Molding, Assembly), analytical testing equipment and/or facility related systems (e.g. Cleanroom, process gases), in accordance with defined requirements, and customer expectations at the Congers, NY facility. The QE will bring a high-level quality mindset to validations and design transfer, ensuring these activities are thoroughly executed and properly documented in compliance with ISO 15378. The employee will also be involved in leading or supporting continuous improvement initiatives. | 09/08/2025 |
| 585 | Nortech Milaca, MN Manufacturing Engineer Bachelors in Engineering Exp: 1 year |
Apply product design, materials and parts, fabrication process, tooling and production equipment, capabilities, assembly methods, and quality control standards knowledge to develop, evaluate, and improve Nortech’s product design, materials and parts, fabrication processes, fixtures, tooling and production equipment capabilities, assembly methods, and quality control standards. Interact with operations, manufacturing, finance and other internal subject matter experts to define, design, test, implement, and support high-quality, efficient, and cost-effective product tooling and manufacturing processes. Apply Lean, Six Sigma, and FOCUS methodologies to assist with analyzing and planning workforce utilization, space requirements, workflow, and designing equipment layout and workspace for maximum quality and efficiency. Coordinate with Quality and work to establish process controls on new products. Review and estimate production times, staffing requirements, and related costs to inform management decisions. Communicate manufacturing capabilities, production schedules, or other information to facilitate production processes. Participate in vendor discussions, evaluate and recommend equipment product specifications and arrange equipment, material purchase, and parts in partnership with internal subject matter experts. | 09/08/2025 |
| 586 | NorthStar Medical Radioisotopes Beloit, WI Radiopharmaceutical Manufacturing Associate (3rd Shift) Bachelor’s Degree (BS) in a STEM discipline Exp: 1 year |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. | 09/08/2025 |
| 587 | Nordisk West Lebanon, NH Manufacturing Technician (Multiple Shifts) Bachelors’ Degree in a science discipline Exp: 0 years |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This is a cleanroom/sterile environment that will require regular gowning, and strict to all procedures in order to ensure the safety of our products for our patients. Prior experience in cleanroom, laboratory, or other sterile environments is a plus, and prior GMP experience is a plus as well. | 09/08/2025 |
| 588 | Novonesis Franklinton, NC Process Engineer I B.S. or M.S. in Mechanical Engineering, Chemical Engineering or Relevant Field Exp: 1-3 years |
We are looking for a dedicated person to provide technical leadership within Supply Chain to ensure products are delivered according to plans within a predictable time frame, volume and quality. You’ll work closely with several departments on site including Quality, Value-Stream (Scheduling), and Operations. You will need an in-depth understanding of our equipment and processes which will be acquired by hands-on experience. On a daily basis you will interact with Operators and Staff members as needed to address and resolve specific product-related or operational concerns. | 09/08/2025 |
| 589 | Novonesis Wausau, WI Assistant Application Scientist Bachelor’s degree in science related field Exp: 0-3 years |
This position works under limited supervision and is responsible for assisting in the Research and Development activities of probiotic powder formulations for encapsulation, powder filling and tableting applications. This position works directly with Product Development and Sales functions. | 09/08/2025 |
| 590 | Novonesis Morrisville, NC Research Associate I Bachelor’s degree in Biology, Microbiology, Biochemistry or related field. Exp: No exp |
We are seeking a Research Associate with a passion for hands-on research and an interest in microbial physiology or fermentation to join our Fermentation Physiology team in the Research Triangle Park, NC. In this role, you will work with a diverse team of scientists and research associates anchored in the global Microbe and Culture Research R&D organization to help in the development of biosolutions for a more sustainable world. As a Research Associate, you will leverage your laboratory skill set to plan, execute and troubleshoot experiments across our core competency areas including cell banking, microbial screening, and fermentation development. | 09/08/2025 |
| 591 | Ocular Therapeutix Bedford, MA Quality Control Chemist I/II Bachelor’s degree in Chemistry or related field Exp: 1-2 years |
Execute routine quality control testing activities as assigned by management. Support CAPA’s, change controls, investigations, and deviations. Participate in the development and validation of analytical methods for Analytical Development group. Participate in testing, project support, data review, ordering of laboratory supplies, and general upkeep of the laboratory. | 09/08/2025 |
| 592 | Orca Bio Sacramento, CA Associate, Cell Therapy Handling and Cryopreservation Bachelor’s degree in Life Sciences, Engineering, or related field Exp: 1-3 years |
The Associate, Cell Therapy Handling and Cryopreservation supports critical operations related to the receipt of patient materials (leukapheresis/blood), cryopreservation of cellular products, and preparation and coordination of final drug product shipments. This role will operate with a deep understanding of GMP manufacturing, cell therapy processes, and the ability to execute multiple tasks in a fast-paced environment. | 09/08/2025 |
| 593 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology (Multiple Positions) B.S. degree in Biological or related sciences Exp: 1 year |
The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned supervisor, commercial manufacturing, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 09/08/2025 |
| 594 | Orca Bio Sacramento, CA Specialist, Quality Assurance Master’s degree in relevant scientific disciplines Exp: 1+ years |
The Specialist, Quality Assurance position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies. | 09/08/2025 |
| 595 | Orchid Orthopedic Solutions Bridgeport, MI Quality Engineer Bachelor of Science (B.S) Exp: No exp |
The Quality Engineer I supports the ongoing quality of Orchid's legacy products & processes and works cross-functionally to sustain the business. | 09/08/2025 |
| 596 | Organogenesis Canton, MA Production Associate I - Apligraf Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 09/08/2025 |
| 597 | Organogenesis Smithfield, RI Production Associate Dermagraft Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Dermagraft), under the direct supervision of the Dermagraft Team Leader/Dermagraft Supervisor/Manager. The Dermagraft Associate will support the Dermagraft Manufacturing department by performing the tasks that will assure the safe and timely processing of Dermagraft, working in both a ISO 7 and ISO 8 cleanrooms. | 09/08/2025 |
| 598 | Embla Medical Orlando, FL Process Improvement Specialist Bachelor’s degree in an Engineering discipline Exp: 1-3 years |
Under the supervision of their manager, the incumbent is responsible for investigation of operational improvement plans, developing, coordinating, and supporting engineering projects with many complex features. Carry out assignments requiring the development of new or improved techniques or procedures. Work on the development of new or improved techniques or procedures and new or refined equipment, materials, processes, products, and/or methods. | 09/08/2025 |
| 599 | PBL Hercules, CA In Vitro Research Assistant I/II/III Bachelor’s Degree in a science-related field (e.g., Biological Sciences, Toxicology, Pharmacology) Exp: 1-3 years |
PBL has immediate openings for a Research Assistant I/II/III in the In Vitro Services Department. The In Vitro Research Assistant is a laboratory level job focusing on the development, optimization, and execution of a variety in vitro (i.e., cell-based and noncell-based) test methods. Successful candidates will be familiar with laboratory procedures including the use of analytical balances, calculating, and preparing dilutions, pipetting, measuring pH, documenting study activities, and analyzing/interpreting data. The In Vitro Research Assistant is expected to perform under minimal supervision. Research Assistants may also contribute to general laboratory operations including equipment maintenance and maintaining a clean and organized laboratory environment. | 09/08/2025 |
| 600 | Paragon Genomics Fremont, CA Technical Operations Associate - Temporary Bachelor's degree in a relevant field (e.g. Biology, Molecular Biology, Biochemistry, Chemistry). Exp: 1+ years |
Paragon Genomics is a fast-growing life sciences company developing advanced reagents and assay kits for next generation sequencing (NGS). We are seeking a Technical Operations Associate to play an important role in the development of novel NGS target enrichment assay technologies and support current operations. This is a laboratory-based role offering strong career growth for a junior or aspiring scientist seeking hands-on molecular biology experience in the NGS field. The position provides an excellent opportunity to work in a multifaceted capacity, building a solid foundation in the biotech industry. | 09/08/2025 |
| 601 | PCI Madison, WI QA Associate I - Operations Bachelor’s degree in a relevant scientific field Exp: 0-2 years |
Join us at PCI as a Quality Associate I – Operations, where you’ll be on the front lines of GMP production—supporting real-time quality oversight, solving problems as they arise, and ensuring that every product meets the highest standards of safety, efficacy, and compliance. This is an ideal role for early-career professionals passionate about science, quality, and continuous improvement. You'll receive hands-on training, mentorship, and exposure to industry best practices while working in a fast-paced, collaborative environment. | 09/08/2025 |
| 602 | PCI Rockford, IL Project Engineer- Drug Delivery Bachelor’s degree in Mechanical, Biomedical, Chemical, or related Engineering discipline Exp: 1-5 years |
As a Project Engineer – Drug Delivery, you’ll play a hands-on, critical role in the design, development, and execution of pharmaceutical packaging and assembly projects. Working closely with engineering, quality, and validation teams, you’ll help deliver high-impact solutions that directly affect patient outcomes around the world. This role supports key product introductions - including high-speed auto-injector lines for diabetes management—giving you the opportunity to work on cutting-edge drug delivery technology. You’ll collaborate with both internal stakeholders and external customers, ensuring projects are delivered on time, on budget, and in compliance with all regulatory standards. This is more than a role—it's a career path. Our Project Engineers have advanced to senior-level roles, including Engineering Manager, based on performance, innovation, and leadership. | 09/08/2025 |
| 603 | PCI Philadelphia, PA Process Engineer I Bachelor’s degree in mechanical, chemical, biomedical, packaging engineering, or a related field Exp: 1-5 years |
PCI is seeking a motivated and detail-oriented Process Engineer I to provide technical leadership in new product launches and continuous improvement initiatives. The ideal candidate will focus on mitigating packaging issues, optimizing production processes, and supporting operational efficiency. This role will involve providing technical and operational support to production, maintenance, and support teams, particularly in the areas of process improvement, equipment modification, optimization, safety, and quality improvement. The Process Engineer I will utilize lean and six sigma techniques and demonstrate excellent organizational and leadership skills in managing projects, equipment needs, staffing projections, and line layout. | 09/08/2025 |
| 604 | Leica Biosystems Richmond, IL Lead Process Engineer Bachelor’s degree in engineering discipline or related degree Exp: 1+ years |
The Lead Process Engineer is responsible for supporting efforts to improve value stream productivity and cost of quality. This role involves coordinating with cross functional teams utilizing the Danaher Business System while maintaining high standards of quality and safety. | 09/04/2025 |
| 605 | Leidos Huntsville, AL Manufacturing Electrical Engineer 2nd shift Masters degree in electrical engineering or other engineering degree Exp: 0-2 years |
As a Manufacturing Engineer you will be overseeing and optimizing the production process, from raw materials to finished products, to ensure efficiency and quality. The type of material is expected to be electronic, electro-mechanical, and mechanical. This position will require frequent coordination with Planning & Production Control, Engineers, and Operations Leads to ensure that material will be available when needed and that proper documentation is in place for floor operations. | 09/04/2025 |
| 606 | Leidos Huntsville, AL Electrical Engineer Masters degree in Electrical Engineering, Math, Physics, or other technical degree Exp: 0-2 years |
Leidos’ Defense Systems RF Systems Portfolio is seeking an Electrical Engineer to join our team of engineers, analysts, and scientists supporting advance radar system analysis in a high-fidelity modeling and simulation environment. Our expertise is setup, test, and evaluation of radar system performance using modeling and simulation of modern air defense systems. | 09/04/2025 |
| 607 | Leidos Huntsville, AL Research Scientist Master’s degree in Electrical Engineering, Math, Physics, or other technical degree Exp: 0-2 years |
Leidos’ Defense Systems RF Systems Portfolio is seeking a Research Scientist to join our team of engineers, analysts, and scientists supporting advance radar system analysis in a high-fidelity modeling and simulation environment. Our expertise is setup, test, and evaluation of radar system performance using modeling and simulation of modern air defense systems. | 09/04/2025 |
| 608 | Leidos Charlotte, NC Transmission Line Engineer Master's degree in Civil, Structural, Electrical, or Mechanical Engineering Exp: 1+ years |
We are seeking a Transmission Line Engineer who will work as a member of a dynamic team working in a fast-paced environment, solving challenging problems involved with electric transmission. The successful candidate will serve as an Engineer on electric transmission line design projects for extra high-voltage (EHV) overhead and underground systems for some of the largest utilities in the country. This employee will apply NESC, ASCE, ACI and other applicable standards in the engineering and design of electrical overhead and underground systems, voltage conversion projects, new capacity projects, and infrastructure replacement projects. Additionally, he/she will perform engineering analyses, prepare bidding documents, draft plans and specifications, and prepare material procurement and construction documents. | 09/04/2025 |
| 609 | Leidos Beavercreek, OH Mechanical Engineer Bachelor’s degree in Mechanical Engineering or similar field Exp: 1-2 years |
This is an exciting opportunity to use your experience to advance the Air Force Research Labs (AFRL) Rapid Technology Development and Demonstrations (RTD2) program. In support of the RTD2 program, your position as a Mechanical Engineer will be to support AFRL programs mature new and emerging technologies and supporting Leidos internal research and development. The position objectives are to provide technical and operational support of new and evolving sensor systems and sensor technologies, provide support for ground and flight demonstrations and tests, and to perform sensor system integration into laboratories, aircraft, and other vehicles/platforms as necessary. | 09/04/2025 |
| 610 | Leidos Huntsville, AL Manufacturing Engineer Bachelor's degree in either Mechanical or Aerospace Engineering Exp: 0+ years |
As a Manufacturing Engineer you will be overseeing and optimizing the production process, from raw materials to finished products, to ensure efficiency and quality. The type of material is expected to be structural, mechanical, and/or electrical components. This position will require frequent coordination with Planning & Production Control, Design Engineers, Manufacturing Engineers at other sites, and Operations Leads to ensure that mBOMs are up to date, lead times are documented, and work order instructions will be available when needed and that proper documentation is in place for floor operations. | 09/04/2025 |
| 611 | Leidos Huntsville, AL Cable Manufacturing Engineer BS degree related to science and engineering (or other technical discipline) Exp: 1 year |
Leidos is seeking a talented Cable Manufacturing Engineer to join a diverse team to create unique solutions for complex problems. With offices across the United States engaging in the defense, space, cyber and commercial fields, Leidos provides responsive, cost-effective engineering, scientific and IT solutions. Candidate will develop, document, and execute manufacturing processes and procedures for cable assemblies and electromechanical products. Use of a Manufacturing Execution System (MES) will be required to create work instructions and develop build strategies. Candidate will support production of cable assemblies and electromechanical assemblies and systems. Applicant will work with a multi-disciplinary team to develop a wide variety of hardware, and work with the latest automated technology used in assembly and test equipment. | 09/04/2025 |
| 612 | LFB Charlton, MA Operations Technician - Animal Facility BS (in related discipline) Exp: 0-1 years |
Daily animal care activities to include: feeding, animal observations/identification of clinical concerns, and nail trimming. Husbandry activities to include cage change/cleaning, use of power wash and chemical dispensing equipment, and general facility sanitization and support. May perform milking of rabbits and standard support activities to meet production goals and adherence to established schedules. Proper basic restraint of rabbits to facilitate general animal care, transfers, and sample collection. Technical skills to include IP injections. May include IM, IV and SC injections. May perform animal identification applications to include ear tags, tattoos and RFID transponders. May provide support for natural and artificial insemination breeding procedures (to include restraint), and kindling/weaning procedures. Utilize computer and paper based systems to accurately document and/or record information to assure compliance with applicable regulations, and company policies. Dependent upon skill level and support needs, may provide veterinary care and animal treatments as assigned. Identify safety issues and initiate corrective actions to reach resolution. Identify and communicate animal welfare concerns. Exhibit a sound understanding of applicable animal care and use guidelines. Weekend and holiday coverage required on a rotating basis. | 09/04/2025 |
| 613 | LG GNS Evansville, IN Associate Chemist Bachelor’s Degree in Chemistry or Related Scientific Field Exp: 1+ years |
The Associate Chemist is responsible for analytical, environmental and physical testing. He or she also performs testing on raw materials and compounded products. This chemist will also participate in the development and formulation of new products under the direction of a Chemist or Senior Chemist. The Associate Chemist may provide any necessary technical support to various other departments. In addition, he or she is responsible for any other task the Chief Technology Officer deems necessary. | 09/04/2025 |
| 614 | Lonza Tampa, FL MSAT Engineer Bachelor’s degree in Science or Engineering Exp: 1-3 years |
The MSAT Engineer ensures that all GMP manufacturing processes are crafted and delivered in a compliant and efficient manner. This role supports the technical and regulatory aspects of assigned projects from inception to completion, including tech transfer and scale-up activities. The engineer collaborates cross-functionally across the organization to facilitate successful project completion aligned with Lonza’s goals. | 09/04/2025 |
| 615 | Lotte Biologics Syracuse, NY Associate Data Engineer Bachelor’s degree in Data Engineering, Data Analytics, Computer Science or related Engineering and/or Analytics Exp: 1-3 years |
The Associate Data Engineer will be responsible for supporting the organization’s data engineering activities, enterprise reporting through Microsoft Power BI, and help maintain IT/OT and data analytics applications. The ideal candidate will have experience in performing ELT/ETL processes using various data engineering tools, have a solid foundation of data warehousing concepts, and know how to build reports/dashboards using Microsoft Power BI. This is a hybrid-based position requiring employee presence, on site 50-100%. | 09/04/2025 |
| 616 | Lotte Biologics Syracuse, NY Assistant Scientist, In-Process Quality Control BS degree in a scientific field Exp: 0-3 years |
The Assistant Scientist, In-Process conducts routine general chemical and biological testing of materials and products for in-process, release and stability purpose, in compliance with all applicable procedures and regulations. A variety of duties are performed by a QC Specialist relating to the efficient and effective functioning of the Quality Control lab. | 09/04/2025 |
| 617 | Lubrizol Painesville Township, OH QC Lab Analyst Bachelor’s degree in chemistry or Related Scientific Field Exp: 1-5 years |
Performs all QC Lab activities, including but not limited to: all Standard Work Process (SWP), Management Systems, and analytical responsibilities. | 09/04/2025 |
| 618 | Mallinckrodt Raleigh, NC Chemical Process Engineer B.S. in Chemical or Mechanical Engineering Exp: 1-5 years |
The Production Engineer will function as a part of the APAP Operations Team. The Production Engineer will apply technical skills to manage day-to-day production, optimize plant operation, resolve operational issues, and investigate process deviations. The Production Engineer will provide technical assistance to the APAP manufacturing employees to ensure that production targets are met while complying with all applicable Safety and Quality rules and regulations. | 09/04/2025 |
| 619 | Mallinckrodt Fenton, MO Supv EHS B.S. degree in Chemical Engineering, Environmental Engineering Exp: 1-3 years |
The primary purpose of the Environmental Health & Safety (EHS) Supervisor is to lead the EHS function at a pharmaceutical tableting facility. Proper execution of this role will help ensure the site is a safe workplace and that it performs in a manner that meets or exceeds the company EHS strategy and expectations. The EHS Supervisor will also champion and collaborate on projects that support the goals and objectives of the site or the Company. | 09/04/2025 |
| 620 | Mallinckrodt St. Louis, MO Quality Assurance Tech II Bachelor’s degree Exp: 1-3 years |
The Quality Assurance Technician II performs a variety of review processes with the intent to correct record errors in manufacturing process documentation that includes batch record review and documentation issue resolution. This role is also responsible for return good inspections, cGMP area inspections and product inspections. This role ensures QA compliance and that cGMP principles are adhered to. | 09/04/2025 |
| 621 | Manifold Bio Boston, MA Research Associate/Senior Research Associate, In Vivo Pharmacology Bachelors or Masters Exp: 1-2+ years |
We are seeking a highly-motivated In Vivo Pharmacology Senior Research Associate who thrives in a fast-paced and creative environment to push the capabilities of our multiplexed in vivo drug discovery platform. Together with senior researchers, you will play a critical role in executing in vivo studies to support internal research projects. This is a hands-on role and you should have extensive experience in multiple aspects of in vivo pharmacology including dosing, necropsy, perfusion, tissue collection and sample processing, among others. The ideal candidate must be able to work effectively both in a collaborative setting and independently. | 09/04/2025 |
| 622 | Matica Biotechnology College Station, TX Microbiologist I, Quality Control BS/BA or greater in sciences, preferably in microbiology, biology, biotechnology, pharmaceutical sciences, or related technical field Exp: 1-2 years |
Matica Biotechnology is currently offering an excellent opportunity for a highly motivated QC professional to join our team. We are looking for someone with expertise in QC Microbiology and gene and cell-based assays preferably with cell and gene therapy experience. The Microbiologist I, QC is responsible for performing environmental monitoring in cleanrooms and for supporting QC Microbiology testing and other lab operations. | 09/04/2025 |
| 623 | Matica Biotechnology Irvine, CA Product Development Associate I Bachelor's or Master's degree Exp: 0-3 years |
The Product Development Associate I is involved in assisting with the planning, conducting and analyzing experiments leading to validation of diagnostic tests in the field of oncology. The PD Associate works in a team and needs to communicate relevant information to professional colleagues and to participate constructively in discussions that will impact the performance of the final product. | 09/04/2025 |
| 624 | Meadowhawk Biolabs Hayward, CA Reseach Associate I - In Vivo Pharmacokinetic Bachelor’s degree in biology, biochemistry, pharmaceutical sciences, or another related scientific field Exp: No exp |
Meadowhawk Biolabs is seeking a highly motivated and dynamic Research Associate to work within the Discovery In Vivo Pharmacokinetic Team at our Hayward, CA location to work with rodent models in a fast-paced team environment. The ideal candidate is driven, hardworking, willing to learn, dedicated, and passionate about science. Given that we are a newly launched Contract Research Organization (CRO) founded by an experienced team of industry veterans, this ground floor position offers unique opportunities for the successful candidate to contribute meaningfully to the creation and development of our services, expand their knowledge base by participation in multidisciplinary teams, and advance their career in capabilities and responsibilities. | 09/04/2025 |
| 625 | Meadowhawk Biolabs Marlborough, MA Research Associate II - LCMS Bachelor’s degree in chemistry, biochemistry, pharmaceutical sciences, or another related scientific field Exp: 1 year |
Meadowhawk Biolabs is seeking a highly motivated and dynamic Research Associate II to work within the Discovery Bioanalytical Team at our Marlborough, MA location to perform LC-MS/MS assays in a fast-paced team environment. The ideal candidate is driven, hardworking, willing to learn, dedicated, and passionate about science. Given that we are a newly launched Contract Research Organization (CRO) founded by an experienced team of industry veterans, this ground floor position offers unique opportunities for the successful candidate to contribute meaningfully to the creation and development of our services, expand their knowledge base by participation in multidisciplinary teams, and advance their career in capabilities and responsibilities. | 09/04/2025 |
| 626 | Medtronic Lafayette, CO R&D Engineer II Masters Degree Exp: 0 years |
In this exciting role as a Sensor R&D Engineer, you will have responsibility for designing and developing patient monitoring consumables for optical physiologic sensing applications. You will contribute across the full product lifecycle, from concept and development through design transfer and sustaining engineering. This includes creating innovative product architectures, prototyping and testing, and developing test methods and tools that ensure product performance and manufacturability. You will collaborate closely with cross-functional partners to deliver clinically meaningful, manufacturable solutions that meet customer needs. | 09/04/2025 |
| 627 | Medtronic North Haven, CT Manufacturing Engineer II Masters degree in Mechanical Engineering and/or Electro-Mechanical Engineering Exp: 0 years |
The Manufacturing Engineer II is responsible for providing daily support of multiple product families with specific regard to product quality, product cost, process development and process improvements, safety, and project management activities in procurement of new forming, grinding, laser drilling machineries, and development of manufacturing equipment validation documentations. Duties include managing and/or participating in cross functional teams to accomplish project specific goals. This position is in North Haven, CT. It is a full-time onsite position. | 09/04/2025 |
| 628 | Medtronic Minneapolis, MN Quality Engineer II Masters Degree in Engineering, Science or technical field Exp: 0+ years |
Are you passionate about ensuring the highest standards of quality in products that save and improve lives? Medtronic is seeking a Quality Engineer II to join our dedicated team at our Plymouth, Minnesota facility, where we design and manufacture mechanical heart valves—Class III Implantable Medical devices that make a direct impact on patients worldwide. This is 100% onsite role at our Plymouth, Minnesota facility. At our Plymouth site, you’ll find a collaborative, mission-driven culture where quality and innovation go hand-in-hand. You’ll work alongside talented engineering and manufacturing professionals, applying your expertise to uphold rigorous quality standards while advancing life-saving cardiovascular technology. | 09/04/2025 |
| 629 | Medtronic Minneapolis, MN Scientist II ; Neuromodulation Masters Degree Exp: 0 years |
Medtronic pioneered the field of neuromodulation with groundbreaking innovations, including the first commercially available spinal cord stimulator (SCS) for chronic pain, the first deep brain stimulation (DBS) system for movement disorders, and the first implantable drug pump for targeted medication delivery to the intrathecal space of the spine. More than 40 years later, we continue to push the boundaries of innovation, constantly challenging ourselves to disrupt the markets we created. By advancing science with bold thinking and collaboration, we bring together the right expertise to engineer groundbreaking therapies and technologies that transform patient care. | 09/04/2025 |
| 630 | Medtronic North Haven, CT Electrical Engineer - I Bachelor’s or Master's Degree Exp: 0 years |
As an Electrical Engineer 1 working on the Surgical Robotics program at the Medtronic, you will be part of a team that develops the electronic hardware for the Robotics Center of Excellence. You will work with other team members in developing, testing, integration, verification, validation, and production transfer of sophisticated electronic systems. Engineers create our market-leading portfolio of innovations. Combine the best of your experience with training and mentorship to move your career forward. If you want a challenging, energizing, rewarding career that changes lives, join us. Help us bring the next generation of life-changing medical technology to patients worldwide. | 09/04/2025 |
| 631 | Medtronic Milwaukee, WI Supplier Quality Engineer II Master's Degree in Engineering, Science or technical field Exp: 0+ years |
Medtronic – Milwaukee, WI manufactures spinal implants and Brain/ENT instrument components. As a member of Supplier Quality Engineering, you will be responsible for management of external suppliers to Medtronic, Milwaukee. You will lead oversight of supplied products, ensuring conformance to purchased material requirements and management of nonconforming product in compliance to Medtronic Purchasing and Supplier Controls, FDA, and international requirements and Quality System Regulations. | 09/04/2025 |
| 632 | Medtronic Northridge, CA Process Engineer II Master's degree Exp: 0 years |
As a member of the Medtronic Diabetes – Continuous Glucose Monitoring Sensor R&D team the Process Engineer II will support the development of next generation CGM products. This position will play a key role in the development of various new/improved chemistry layers/coatings of glucose sensors by designing and executing design feasibility, process development, and manufacturing transfer. This role will be responsible for driving the product build documentation, design and executing experiments and builds of sensors for pilot scale evaluations, execute data trending & statistical analysis. Upon successful process and design optimization, this role will subsequently support tech transfer to new product introduction and manufacturing teams. You will manage deliverables for multiple projects and maintain an effective system for tracking progress. You will be interfacing with Managers, Engineers &Technicians in R&D and New Product Introduction (NPI) Operations teams as well as Quality and Clinical groups to accomplish day to day activities. The candidate must have strong organizational skills, attention to details, an analytical mindset and ability to communicate effectively with multiple stakeholders. | 09/04/2025 |
| 633 | Molecular Designs Littleton, MA Manufacturing Test Engineer I Bachelor of Science degree in Electrical Engineering, Robotics Engineering, or equivalent Exp: 0-2 years |
The Manufacturing Test Engineer I will provide hands-on electrical engineering support for Mevion’s manufacturing operation, focused on proton therapy systems. This entry-level position involves assisting with the development and maintenance of production test setups, improving test documentation, investigating failures, and supporting continuous quality and process improvements across internal and supplier environments. | 09/04/2025 |
| 634 | Micro Systems Engineering Lake Oswego, OR Senior Engineer - Design and Development Master’s degree in Electrical Engineering, Applied Physics, or related Engineering field Exp: 6 months |
Develop, implement, and qualify new supply chain and technology platforms that enable MSEI to meet its product quality, reliability, volume, delivery, and cost objectives. Define and deploy new technology platforms in a cross-functional team for new product applications through testing, simulation, prototypes, and volume manufacturing. Use systematic problem-solving approaches to resolve quality/performance issues with suppliers, development, and manufacturing teams. Lead testing and validation of platforms for high reliability applications, by performing use case based electrical, environmental stress tests, and process limit studies. Perform implementation tasks, including leading stage-gate approvals, documentation, supplier quality interface, characterization, verification and on-going sustaining support in a highly automated manufacturing environment. | 09/04/2025 |
| 635 | Mikart Atlanta, GA Quality System Specialist Bachelor’s degree in a scientific/technical discipline Exp: 1-5 years |
The Quality Systems Specialist is responsible for the timely and accurate maintenance of vendor qualifications, complaints and adverse event investigations, and oversight of training in support of drug product development and production. | 09/04/2025 |
| 636 | Minaris Allendale, NJ QC Microbiology Analyst I BA/BS in a science or relevant field Exp: 0-2 years |
The Quality Control Microbiology Analyst I (6:30AM-5:00PM Sunday -Wednesday) serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. | 09/04/2025 |
| 637 | Moderna Cambridge, MA Senior Research Associate, Flow Cytometry Core M.S. in Immunology, Cell Biology, or a related life science field Exp: 0+ years |
We are seeking a highly motivated and detail-oriented Senior Research Associate to join our Flow Cytometry Core Team. The successful candidate will play a critical role in supporting method development and execution of high-throughput flow cytometry experiments, and tissue-based sample preparation. This role offers the opportunity to contribute directly to cutting-edge discovery and translational research programs through high-quality technical execution and scientific collaboration. | 09/04/2025 |
| 638 | Molecular Designs Birmingham, AL Lab Technician - Night Shift Bachelor’s degree in Biology, Chemistry, Biochemistry Exp: 6 months |
We're looking for a Molecular Lab Technician (MLT) to help with day-to-day screening procedures for our molecular testing laboratory. We’re seeking a highly driven, motivated, and experienced Lab Technician that understands the PCR process, its importance, and work through each complex step with the upmost efficiency. The ideal Lab Technician will have patience, empathy, time management, and professionalism with patients, co-workers, and providers. | 09/04/2025 |
| 639 | Moog Buffalo, NY Systems Engineer Master of Science Degree in Engineering Exp: 1+ years |
Moog is currently hiring a Systems Engineer in our Space and Defense Group. Come join a leading global supplier of motion control and electronic solutions! | 09/04/2025 |
| 640 | Lilly Lebanon, IN Manufacturing Scientist - LP1 Peptide Synthesis Master's degree in STEM Discipline (Chemistry preferred) Exp: 1 year |
The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 09/04/2025 |
| 641 | Lilly Lebanon, IN Sterility Assurance Scientist - Advanced Therapies Manufacturing Bachelors in Microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline Exp: 1+ years |
Sterility Assurance – Technical Services/Manufacturing Scientist (TS/MS) role is a technical position that develops and implements the site’s sterility assurance related initiatives and provides technical leadership with regard to sterility assurance & environmental monitoring strategies. Primary objectives include the start-up and compliant manufacturing of gene therapy drug product and drug substance, particularly as it relates to development and implementation of sterility assurance strategies, including environmental monitoring, aseptic process simulations, facility cleaning, facility sanitization, and sterility assurance risk management. | 09/04/2025 |
| 642 | Lilly Indianapolis, IN Chemist, Oligonucleotide Chemistry Bachelors and/or Masters in Organic Chemistry, Chemistry, Biochemistry, or a related field Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for a collaborative, creative and energetic problem solver to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to accelerate the core capabilities and development of internal RNAi-based clinical candidates. | 09/04/2025 |
| 643 | Lilly Indianapolis, IN Engineer - TS/MS Device Assembly & Packaging, DPEM Bachelors Degree in Engineering (strongly preferred), Chemistry, Pharmacy or similar STEM related fields Exp: 1+ years |
This role is a member of the Technical Service Manufacturing Science function within the Drug Product External Manufacturing organization (DPEM). This role is responsible for all technical activities related to the support of external manufacturing as defined in the Global Contract Manufacturing Standards. This role is the process expert for the step(s) of the product(s) and process(es) for each contract manufacturing relationship with focus on Device Assembling and Packaging. This role is a member of the joint process team (JPT) and has direct responsibility for oversight of the day-to-day operations and technical agenda at the CM. | 09/04/2025 |
| 644 | Integer Plymouith, MN R&D Engineer I Bachelor’s degree in an engineering or related technical field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves general engineering methods and tools. As an entry level engineer, you will ensure that Integer’s internal and external customer expectations are met or exceeded with the direction, instruction and guidance from more experienced engineers and managers in your organization. | 08/25/2025 |
| 645 | Integer Palm Harbor, FL Engineer I - Product Development/Design Bachelor’s degree in a related field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves conventional engineering practice. Ensures Integer’s internal and external customer expectations are met or exceeded. | 08/25/2025 |
| 646 | Integra San Francisco, CA Systems Engineer I/II Bachelor’s or Master’s degree in Biomedical Engineering, Mechanical Engineering, Biochemistry, Chemical Engineering, or a related discipline Exp: 1-3+ years |
INTEGRA Microfluidics is seeking a highly motivated, hands-on Systems Engineer I/II to join our team and work on next-generation sequencing (NGS) and microfluidics projects. The successful candidate will work closely with senior engineers and scientists to develop and optimize novel microfluidic-based systems for various applications. | 08/25/2025 |
| 647 | Integra LifeSciences Plainsboro, NJ Engineer II, Continuous Improvement Masters degree in Industrial Engineering, Manufacturing Engineering, or a related field Exp: 0-2 years |
The Engineer II, Continuous Improvement will play a crucial role in driving and facilitating process improvement initiatives across the organization. This role involves analyzing current processes, identifying areas for enhancement, and implementing strategies to increase efficiency, reduce waste, and improve overall operational performance. The ideal candidate will have a solid background and understanding in process improvement methodologies, excellent analytical skills, and the ability to lead cross-functional teams. The engineer will initiate and support implementation activities for changes approved within Integra’s change management program. The Continuous Improvement Engineer II will work within cross-functional core teams on the development of new products ensuring on-time transfer of new products to production. This is an individual-contributor position. | 08/25/2025 |
| 648 | Integra LifeSciences Plainsboro, NJ Clean Room Manufacturing Operator Bachelors Degree in related science Exp: 0-2 years |
This Clean Room Manufacturing Operator role will include processes such as enzymatic treatment of collagen, alkali treatment of collagen, tendon collagen prep, dispersion preparation, and lyophilization. It is essential to perform these tasks meticulously to ensure the quality of our products. Additionally, you will be responsible for the setup, operation, and cleaning of all clean room manufacturing equipment. This entails working in ISO Class 5 or ISO Class 7 areas and adhering to Clean Room gowning protocols. All operations must be conducted in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOPs), and Health and Safety requirements. Operating in a team environment, we emphasize daily achievements and maintaining high-quality standards in our production processes. Your dedication and attention to detail will play a valuable role in our success. | 08/25/2025 |
| 649 | Integra LifeSciences Braintree, MA Sr. Manufacturing Quality Engineer l Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
This position is for a Sr. Manufacturing Quality Engineer l with hands-on experience and proven success in managing Quality systems. The successful candidate will be responsible for partnering with sterilization and microbiology Subject Matter Experts to assist in root cause investigations related to sterility and microbiological outputs, review and assess the accuracy and sustainability of process requirements as they pertain to sterility assurance and microbiology and drive cross-functional collaboration with quality groups across the organization. This role requires a strong quality mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring product safety and compliance. The ideal candidate should demonstrate proficient experience with quality management concepts including but not limited to eQMS, risk assessment, PFMEAs, process controls, root cause investigations, CAPA, and continuous improvement | 08/25/2025 |
| 650 | Integra LifeSciences Princeton, NJ Sr. Supplier Quality Engineer l Master's degree in engineering, or Sciences Exp: 0-2 years |
This position is for a Sr. Supplier Quality Engineer l – Global Supplier Quality with hands-on experience and proven success in managing Supplier Quality systems. The successful candidate will be responsible for partnering with sterilization and microbiology Subject Matter Experts to assist in root cause investigations related to supplied services and/or processes, review and assess the accuracy and sustainability of supplier requirements as they pertain to sterility assurance and drive cross-functional collaboration with supplier quality groups across the organization. This role requires a strong quality mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring product safety and compliance. The ideal candidate should demonstrate proficient experience with quality management concepts including but not limited to supplier quality audits, eQMS, risk assessment, process qualification, process controls, root cause investigations, CAPA, and continuous improvement | 08/25/2025 |
| 651 | Integra LifeSciences Plainsboro, NJ Microbiology Technician I Bachelor’s degree, in Microbiology or Biology Exp: 0-3 years |
The Microbiology Technician I will provide support to the QC Microbiology Laboratory as pertaining to the respective responsibilities. Performs functions such as executing laboratory testing for in-process and finished good products, water, stability studies, and validation studies as well as performs environmental monitoring. This position is responsible for operating in compliance with all applicable procedures and policies | 08/25/2025 |
| 652 | Integra LifeSciences Braintree, MA Quality Design and Reliability Assurance (DRA) Engineer II Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
The Quality Design and Reliability Assurance (DRA) Engineer II is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, specifically the Boston/ Braintree site. The role contributes and supports the design and development of new and improved products. The (DRA) Engineer II will interact with external design and development partners, participating on cross-functional project teams through all phases of the product development process, and assisting the technical team with planning, executing, documenting, and communicating testing activities. The role works with Product Development, Project Management, Regulatory, Marketing and Medical Affairs. | 08/25/2025 |
| 653 | Integra LifeSciences Princeton, NJ Sr. Design Quality Engineer I Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
This position is for a Design Quality Engineer l with hands-on experience and proven success in managing Design Quality systems. The successful candidate will be responsible for partnering with sterilization and microbiology Subject Matter Experts to assist in root cause investigations related to sterility and microbiological design outputs, review and assess the accuracy and sustainability of product requirements as they pertain to sterility assurance and microbiology and drive cross-functional collaboration with design quality groups across the organization. This role requires a strong quality mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring product safety and compliance. The ideal candidate should demonstrate proficient experience with quality management concepts including but not limited to eQMS, risk assessment, DFMEA, process controls, root cause investigations, CAPA, and continuous improvement | 08/25/2025 |
| 654 | Integral Molecular Philadelphia, PA Research Associate Bachelor’s degree in biology, bioengineering, or a related field Exp: 1-2 years |
Perform assigned tasks in the lab, including cell culture, DNA handling, and flow cytometry in a 384-well format, as well as the associated data analysis. Operate liquid-handling robots to perform antibody stains, washes, and dilutions, while troubleshooting both experimental and equipment-related issues. Follow standard operating procedures (SOPs) to complete experiments and assays with accurate record keeping, and assist in the preparation of customer-facing reports and deliverables. Independently plan and manage a daily schedule, often balancing multiple projects simultaneously, and present experimental data at both team and company-wide meetings. | 08/25/2025 |
| 655 | Integral Molecular Philadelphia, PA Research Technician Bachelor's degree in Biology, Chemistry, medical technology or related field Exp: 6 months-2 years |
Set up and execute routine laboratory experiments, perform DNA isolation and associated quality control assays, maintain plasmid library using high throughput techniques, perform tasks using aseptic techniques including working within a biological safety cabinet, and organize large data sets within an Excel spreadsheet. | 08/25/2025 |
| 656 | Integrated DNA Technologies (IDT) Coralville, IA QA Complaint Analyst Bachelor's degree in Biological Sciences or related field (e.g., Biomedical Engineering, Systems Engineering, Pharmacology, Chemistry) Exp: 1-2 years |
This position is part of the Quality Assurance Department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. | 08/25/2025 |
| 657 | Integrated DNA Technologies (IDT) Boulder, CO Manufacturing Technician II Bachelor's degree in a science related field (Biology, Genetics, Chemistry or related life science field) Exp: 1 year |
The Manufacturing Technician II is responsible for manufacturing next-generation sequencing reagents and kits, working both independently and as part of a team in concordance with established procedures and ISO 13485 guidelines. This position reports to the Manufacturing Supervisor and is part of the xGen Manufacturing team located in Boulder, Colorado and will be an on-site role. | 08/25/2025 |
| 658 | IMI Pompano Beach, FL Engineer I Bachelor’s degree in mechanical engineering, or equivalent Exp: No exp |
Engineer I is the entry level engineering position for product development. The Engineer will work under the direct supervision of a manager and/or more experienced team members, to design, prototype, inspect and test specific components and assemblies of a medical device, while creating & maintaining compliant documentation for tasks preformed. The position is intended to prepare engineers new to the medical device industry for advancement to the next level of Engineer II. | 08/25/2025 |
| 659 | Inventprise Woodinville, WA Manufacturing Associate I - 1st Shift Bachelor’s degree Exp: 0-3+ years |
The Manufacturing Associate I is responsible for executing and monitoring manufacturing processes on the plant floor. They are also learning and becoming familiar with navigating Inventprise Quality Systems and will provide information to help support the reporting of administrative and compliance related tasks including: nonconformance investigation and report writing, generation and execution of CAPAs, and revision and creation of batch records and standard operating procedures. | 08/25/2025 |
| 660 | Inventprise Woodinville, WA Manufacturing Associate I - 2nd Shift Bachelor’s degree Exp: 0-3+ years |
The Manufacturing Associate I is responsible for executing and monitoring manufacturing processes on the plant floor. They are also learning and becoming familiar with navigating Inventprise Quality Systems and will provide information to help support the reporting of administrative and compliance related tasks including: nonconformance investigation and report writing, generation and execution of CAPAs, and revision and creation of batch records and standard operating procedures. | 08/25/2025 |
| 661 | Invivoscribe San Diego, CA Quality Control Laboratory Associate I B.S. degree in a scientific discipline Exp: 0-2 years |
We are looking to add a Quality Control Laboratory Associate I is responsible for ensuring that only quality products are released for distribution. It is a QCLAI’s job to ensure that products are tested to meet the applicable government regulations and industry standards, and to maintain GMP environment. The Quality Control Laboratory Associate is also responsible for data entry. | 08/25/2025 |
| 662 | IQVIA Ithaca, NY Scientist, Lab Operations Bachelor's degree in applied/laboratory sciences Exp: 0-2 years |
We are seeking a Scientist, Lab Operations to join Q2 Solutions, IQVIA’s laboratory business at Ithaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Join our scientific team to execute laboratory procedures and contribute to research excellence while maintaining compliance with GLP standards. You’ll play a key role in analyzing data and supporting projects that impact global health. | 08/25/2025 |
| 663 | IQVIA Durham, NC Clinical Research Associate, Obesity/Diabetes/GLP-1 (Full Service) Bachelor's Degree in scientific discipline or health care Exp: 1 year |
IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) clinical trials. Phase 1 experience is a plus! Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. | 08/25/2025 |
| 664 | IQVIA Ithaca, NY Associate Scientist, Sample Preparation Bachelor’s Degree in a Life Sciences discipline Exp: 6 months |
We are seeking an Associate Scientist to join IQVIA Laboratories in Ithaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments and the preparation of solutions and reagents. | 08/25/2025 |
| 665 | IQVIA Valencia, CA Laboratory Technical Specialist Bachelor's Degree in life sciences or other relevant field Exp: 1 year |
We are seeking a Laboratory Technical Specialist to join Q2 Solutions, IQVIA’s laboratory business at Valencia, CA We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. You will lead the production and development of specialized reagents for digital ELISA assays, collaborating cross-functionally to drive product transfer and support diagnostic assay manufacturing. This is a fully on-site position. | 08/25/2025 |
| 666 | IQVIA Indianapolis, IN QA Auditor 1 Bachelor’s degree Exp: 1 year |
We are seeking a QA Auditor 1 to join Q2 Solutions, IQVIA’s laboratory business at Indianapolis, IN. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Support quality assurance efforts by assisting in the coordination, documentation, and execution of audits under the direction of senior QA staff. This role ensures regulatory compliance and strengthens operational excellence within a dynamic laboratory setting. | 08/25/2025 |
| 667 | Johnson & Johnson Santa Clara, CA R&D Project Manager I (Sustaining) - Shockwave Medical BS/BA in science, engineering Exp: 1-2 years |
The R&D Project Manager I is responsible for managing PMO initiative projects by coordination of cross functional project activities to ensure projects achieve desired outcomes. Under guidance and direction, this role will be responsible for supporting the successful implementation of best practices throughout the project lifecycle. | 08/25/2025 |
| 668 | Johnson & Johnson Raritan, NJ GTO Associate Pkg Development Engineer Bachelor’s Degree in Package Engineering or Technical Degree (Mechanical, Chemical, Biomedical Engineering, etc.) Exp: 0-2 years |
The Primary Engineer will be designing, developing and testing sterile barrier packaging systems for J&J Medtech at Ethicon Inc. This role will support both New Product Development and Lifecycle Management teams. | 08/25/2025 |
| 669 | J-STAR Research Cranbury, NJ Research Scientist Master in Chemistry, Chemical Engineering, Pharmaceutical Chemistry, or Food Science Exp: 1 year |
Pharmaceutical Ingredient (API), intermediates, impurities, starting material and excipients from drug substances and drug products. Analyze organic and inorganic compounds to determine chemical or physical properties, composition, structure, relationships, reactions, using chromatography, spectroscopy, spectrophotometry techniques including HPLC, UPLC, IC, GC, MS, UV, XRPD, DSC, TGA, NMR, and KF. Design and perform method verification and validation. Determine the specificity, linearity, accuracy, precision, forced degradation, robustness of the methods. Collect and analyze data, and maintain data integrity under GMP, GLP, and FDA regulations. Prepare documentation of test procedures and technical reports. Prepare, review, and/or approve methods, protocols, and development reports. Maintain laboratory instruments to ensure proper working order. Apply scientific expertise to troubleshooting, laboratory investigation and problem resolution. Participate in maintaining high quality laboratory environment and comply with Health, Safety and Environmental responsibilities for the position. | 08/25/2025 |
| 670 | J-STAR Research Cranbury, NJ Research Scientist of Crystallization R&D MS or BS. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field Exp: 1-5 years |
We are seeking a highly motivated and skilled Research Scientist to join our Crystallization R&D Department at Porton J-STAR. In this role, this position is responsible for leading group or contributing individually to conduct Solid Form Studies and pre-formulation will search for the right solid form and develop formulations to support preclinical and Phase I studies including PK, PD, efficacy, tox studies. This role is also responsible for Crystallization Process Development will develop crystallization processes to define and control final solid form of drug substances with desired solid-state attributes needed for optimum performance as well as drug intermediates for robust purification. The responsibilities of the position include, but are not necessarily limited to, the items listed below. | 08/25/2025 |
| 671 | Jubilant HollisterStier Seattle, WA Weekend Shift Process Engineer I, II, III, & Sr. Bachelor’s of Arts or Science with a major in Biology, Chemistry, Physics, or Engineering Exp: 0-5 years |
The weekend shift Process Engineer I/II/III/Sr. provides ownership and focus for pharmaceutical processes and technical transfers at Jubilant HollisterStier. This position will engage in and manage projects and multi-disciplinary teams with direct supervision. The process engineer will also contribute technical direction for complex projects and exhibit clear communication skills with all levels of employees. | 08/25/2025 |
| 672 | Jubilant HollisterStier Spokane, WA Manufacturing Specialist Bachelors Exp: 1-5 years |
The Manufacturing Specialists direct train schedule and coordinate daily production within multiple areas of Raw Materials department. Ensure technician training is completed in a timely manner, perform technician training and review documentation. Ensure all resources and supplies are available for day-to-day operations. | 08/25/2025 |
| 673 | Jubilant HollisterStier Spokane, WA Microbiologist I/II Bachelor of Science in Microbiology or related hard science with microbiology emphasis Exp: No exp |
The QC Microbiologist I/II performs the microbial analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw materials/product disposition. | 08/25/2025 |
| 674 | Jubilant HollisterStier Spokane, WA Environmental Monitoring Specialist Bachelors of Science Exp: 1 year |
The Environmental Monitoring Specialist performs the functions associated with sampling, initiating tests, collecting and evaluating test results related to defined quality parameters for surface, air, personnel, product and utility systems such as compressed gases and WFI. The Specialist oversees EM functions and personnel, schedules projects, tasks and personnel, assists in training EM technicians and gown training of all aseptic personnel. | 08/25/2025 |
| 675 | KBI Biopharma Durham, NC Microbiology Associate I/II Bachelor’s/Master’s degree in Microbiology, Biology or related technological field of science Exp: No exp |
Testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. This person is responsible for the aspects of the following programs as directed by management: Environmental Monitoring (Air Viable, Total Air Particulate, Surface Viable); Clean Utility Monitoring (Water Sampling, Bioburden, Conductivity, TOC, Coliform and Nitrates); Compressed Gas Monitoring (Collection, Air Viable, Total Air Particulate, Dragger Tests and specific ID tests); Product Testing (Bioburden, Endotoxin, Host Purity, or Non-Host); Media Release; Laboratory Support. It is the expectation that this position is required to be onsite full time. Addition, this position should be in the laboratory/facility for a minimum of 75% time daily. Second Shift: Sunday - Wednesday [2:00 PM EST - 12:00 AM EST]. | 08/25/2025 |
| 676 | KBI Biopharma Durham, NC Downstream Manufacturing Associate I/II Bachelor’s degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment. | 08/25/2025 |
| 677 | KBI Biopharma Durham, NC Manufacturing Associate l/ll Bachelor’s degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment. | 08/25/2025 |
| 678 | KBI Biopharma Durham, NC QA Specialist I- Quality Engineering Bachelor’s degree Exp: 1-3 years |
The Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing Process and Areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA Specialists are expected to provide sound guidance to Manufacturing with respect to process, SISPQ of product, and risk. MQA Specialists share responsibility for the inspection readiness of the site. MQA Specialists routinely work on the cleanroom floor directly with the Manufacturing team to provide real time guidance and support. Specialists routinely collaborate with Manufacturing and work on team initiatives. The MQA Specialist may also be responsible for coaching and mentoring as needed to foster a GMP compliant site. | 08/25/2025 |
| 679 | KBI Biopharma Durham, NC Research Associate II Master’s degree in chemistry, biochemistry or related area Exp: 0+ years |
Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical Development (AD) Department. The individual in this position will be responsible for executing experimental protocols and performing data analysis in biopharmaceutical laboratories. | 08/25/2025 |
| 680 | Kindeva Bridgeton, MO Quality Engineer Master’s degree in a scientific or engineering discipline Exp: 1-3 years |
In this role, you will develop, direct, and lead Quality oversight for process improvements in equipment and material preparation, aseptic compounding, filling, inspection, and packaging at the Brentwood, Maryland Heights, and Bridgeton facilities. You will coordinate support activities, reviews, audits, and the release of semi-finished products and components to align with site-wide objectives. You will collaborate with cross-functional teams to support continuous improvement initiatives, incident investigations, and change management. Additionally, you will make decisions related to Incident Investigations and Corrective and Preventive Actions, ensuring a focus on overall quality, site priorities, and operational success. | 08/25/2025 |
| 681 | Kindeva Woodbury, MN Product and Process Development Scientist Bachelor’s degree in a science discipline Exp: 1 year |
This is an exciting role within an expanding team of process and product development specialists and offers the successful candidate an opportunity to make a significant contribution to the development of new inhalation products. The person hired for the position of pMDI Product and Process Development Scientist will support the development and testing of pMDI pharmaceutical products. | 08/25/2025 |
| 682 | Krystal Biotech Pittsburgh, PA Clinical Trial Associate/Clinical Research Coordinator BS/BA degree required in science/health-related field Exp: 1-3 years |
Krystal Biotech, Inc. is seeking a Clinical Trial Associate to support our Clinical Operations Team. The Associate's responsibilities will entail, but not be limited to, assisting with the management and inventory of clinical supplies, ensuring proper materials are available at clinical sites in a timely manner, and working with the Clinical Operations team to support multiple Clinical Trials. Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. | 08/25/2025 |
| 683 | Krystal Biotech Moon Township, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 08/25/2025 |
| 684 | Getinge Wayne, NJ Quality Systems Data Analyst Bachelor’s Degree in Engineering, Data Analytics, or related field Exp: 1-3 years |
We are seeking a results-driven and detail-oriented Data Analyst to support our Quality organization. This hybrid role plays a key part in driving data-informed decision-making and leading strategic quality initiatives across the organization. The ideal candidate will analyze quality data trends, lead process improvement projects, and ensure compliance with applicable medical device regulations and standards. The position supports the Cardiac Surgery business and is a hybrid role with a minimum of 3 days onsite at the Wayne, NJ headquarters. | 08/19/2025 |
| 685 | Getinge Wayne, NJ Engineer I, Production Bachelor’s degree in Manufacturing/Industrial, Mechanical, Biomedical Engineering or Instrumentation (Electrical Engineering) Exp: 1-2 years |
Supports production area in tooling design, process improvement, and cost improvement. | 08/19/2025 |
| 686 | Gilead Foster City, CA Sr Research Associate, Medicinal Chemistry Masters degree Exp: 0+ years |
As a Sr. Research Associate, you will participate a multi-disciplinary drug discovery team through the design and synthesis of new molecules. The successful candidate will have an excellent track record and a commitment to tackling drug discovery challenges through organic synthesis. | 08/19/2025 |
| 687 | Gilead Foster City, CA Research Associate, Medicinal Chemistry Bachelors degree Exp: 0+ years |
As a Research Associate, you will participate on a multi-disciplinary drug discovery team through the design and synthesis of new molecules. The successful candidate will have an excellent track record and a commitment to tackling drug discovery challenges through organic synthesis. | 08/19/2025 |
| 688 | Gilead Foster City, CA Sr Research Associate, Drug Metabolism MS degree in pharmacology, pharmaceutical sciences, cell biology, biochemistry, or relate Exp: 0+ years |
The primary responsibility of the Drug Metabolism and Pharmacokinetic (DMPK) Senior Research Associate role is to conduct absorption, distribution, metabolism, and excretion (ADME) studies to support the discovery and development of drugs candidates. As a member of the DMPK department, the candidate will conduct laboratory experiments (biochemical or cell-based) and bioanalysis (LC/MS and other methods), interpret data, and contribute to understanding of the ADME properties of small molecules. | 08/19/2025 |
| 689 | Gilead Oceanside, CA Senior Research Associate, Biologics Pivotal Formulation & Process Development MA / MS Degree in Pharmaceutical Science, Chemistry, Biochemistry, Chemical Engineering, or related scientific fields Exp: 0+ years |
We are seeking a highly motivated, attentive, and self-driven candidate to join our team, Biologics Pivotal Formulation and Process Development, as a Senior Research Associate. Once onboarded, the successful candidate will contribute in developing formulation and drug product processes for innovative molecules. The candidate will have tremendous opportunities for career growth in a fast-paced and resource-rich environment through training and professional relationships. The ideal candidate is expected to be action oriented with high expectations of themselves and others. S/he should have good verbal and written communication interpersonal skills. | 08/19/2025 |
| 690 | Gilead Foster City, CA Research Associate, Analytical Ops BS or BA degree in Chemistry, Biology or relevant science/engineering majors Exp: 0-2 years |
We are seeking a highly motivated, attentive, and self-driven candidate to join the Method Validation and Transfer team in Global Small Molecules. The successful candidate will contribute to the method validation of drug substance, drug product intermediate and drug product to support early phase clinical projects. The candidate will have opportunities for career growth through acquisition of new skills, experiences, and GMP knowledge in a fast-paced and resource-rich environment. The ideal candidate is expected to be action oriented and should possess good verbal and written communication and interpersonal skills. | 08/19/2025 |
| 691 | Globus Medical Audubon, PA Associate Project Engineer - Sustaining Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related field Exp: 0-3 years |
Design and implement product line extensions, working closely with the R&D, clinical, and regulatory teams. Champion Design for Manufacturing (DFM) improvements across launched product lines to optimize cost, reliability, and manufacturability. Resolve manufacturing challenges through vendor coordination and iterative design updates. Provide technical support during cadaver labs and customer engagement meetings to validate and refine device performance. Support surgical cases in the operating room, working directly with surgeons to gather real-time feedback and identify clinical opportunities for improvement. Perform product scrap analysis and coordinate remediation strategies to improve yield and performance. Conduct complaint evaluations, identify root causes, and implement corrective actions in collaboration with cross-functional teams. Lead and contribute to Post-Market Surveillance Reports (PMSR) and Periodic Safety Update Reports (PSUR) in compliance with global regulatory standards. Drive risk analyses to assess and mitigate design and process risks. | 08/19/2025 |
| 692 | Globus Medical West Carrollton, OH Manufacturing Engineer Masters degree in an engineering discipline Exp: No exp |
As a Manufacturing Engineer, you will develop, implement and maintain methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies and final assemblies. Support new initiatives and productivity targets for given manufacturing processes. Interface with design engineering in coordinating the release of new products. Estimate manufacturing cost, determine time standards and make recommendations for tooling and process requirements of new or existing product lines. Maintain records and reporting systems for coordination of manufacturing operations. | 08/19/2025 |
| 693 | Globus Medical Audubon, PA Regulatory Associate Bachelor’s degree in health or science-related field, or equivalent; Engineering degree is a plus Exp: 0-2 years |
The Regulatory Affairs Associate assists in drafting, submitting and gaining clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requiring working knowledge of products under review and of relevant regulations and guidance documents. This individual must be enthusiastic, positive, even-tempered and effective in building working relationships with internal teams while following FDA 21 CFR regulations. | 08/19/2025 |
| 694 | GRAM Grand Rapids, MI QC Chemist I (1st shift/Group B) Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology) Exp: 1-3 years |
The QC Chemist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 08/19/2025 |
| 695 | GRAM Grand Rapids, MI Finishing Shift Lead (2nd shift) BS or BA in Biopharmaceuticals, or other Life Sciences field Exp: 1 year |
Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day! | 08/19/2025 |
| 696 | GRAM Grand Rapids, MI QC Microbiology Technician (2nd shift) Bachelor’s degree in Microbiology or a related field Exp: 0-2 years |
The QC Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. | 08/19/2025 |
| 697 | GRAM Grand Rapids, MI QC Microbiology Technician (3rd shift) Bachelor’s degree in Microbiology or a related field Exp: 0-2 years |
The QC Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. | 08/19/2025 |
| 698 | GRAM Grand Rapids, MI QC Chemist I (2nd Shift/Group A) Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology) Exp: 1-3 years |
The QC Chemist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 08/19/2025 |
| 699 | GRAM Grand Rapids, MI Environmental Health & Safety Specialist I or II Bachelor’s or Master's degree Exp: 0-3 years |
The Environmental Health & Safety (EHS) Specialist I or II works with EHS Department to review and interpret regulatory requirements, relating to EHS, and provide cost effective recommendations to the EHS Manager for implementation and compliance. The EHS Specialist I performs a variety of complex tasks and assist in the work of others. The EHS Specialist II performs a variety of complex tasks and may lead and direct the work of others. A fair degree of creativity and latitude is expected with either the level I and/or level II role. This is an on-site position. | 08/19/2025 |
| 700 | Grifols Clayton, NC Assistant/Associate/Senior Biologist BS/BA degree in a life science field, medical technology, or related Exp: 6months |
The incumbent is responsible for performing complex laboratory analysis of plasma and plasma products in a GMP laboratory. Responsibilities include sample accessioning, sample preparation, reagent preparation, testing, result calculation, as well as quality control of assays and equipment. The incumbent will also support assay validation, method transfer, reagent and control qualification, and laboratory maintenance activities as assigned. Must be comfortable working with infectious material on a daily basis. Person must be able to work in a biological safety cabinet and comfortable working with a microscope for several hours at a time. Candidates for the position must be proficient with using micropipettes and serological pipettes while making dilutions and serial dilutions. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform their share of cleaning duties and housekeeping. | 08/19/2025 |
| 701 | Grifols Clayton, NC Engineer - Validation I Bachelors Degree in Engineering Exp: 0-2 years |
The Engineer I - Validation / Engineer II – Validation / Validation Specialist I / Validation Specialist II / Sr. Validation Specialist I position supports Fractionation, Purification, Filling, Utilities and/or capital projects as required. This position is responsible for assigned qualification and validation related activities related to supporting the Clayton NC site. | 08/19/2025 |
| 702 | GSK Cambridge, MA Associate Scientist Analytical Chemistry MS Exp: 1+ years |
As Associate Scientist/Sr. Associate Scientist, Analytical Chemistry, you and your team will play an important role in the analysis and quality control of GSK’s preclinical pipeline. You will maintain and troubleshoot analytical equipment and execute diverse analytical methods for small molecules and oligonucleotides to help accelerate GSK’s pipeline and platform technology ambitions. | 08/19/2025 |
| 703 | Guardant Health Redwood City, CA Biospecimen Associate I Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field Exp: 1-2 years |
The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow. | 08/19/2025 |
| 704 | Hikma Pharmaceuticals Dayton, OH Quality Assurance Associate Bachelor’s Degree in Science Exp: 1-2 years |
Under the supervision of the Quality Assurance Supervisor, this person is responsible for performing field QA activities: in process checks in the aseptic processing area, approval for area clearance, AQL inspection for finished products, retention sampling for finished products, batch record review, final product release, review and approve operation documents and forms, and approval / rejection of in-coming raw materials, components, and final product labels. Ensure compliance of operations personnel with the company’s procedures and Good Manufacturing Practices (GMPs). This position will also be responsible for identifying any deviations or non-conformances, writing deviation reports, performing root cause analysis, writing/revising standard operating procedures and forms, and tracking metrics, when required. | 08/19/2025 |
| 705 | Hikma Pharmaceuticals Cherry Hill, NJ QA Inspector Bachelor’s Degree Exp: 0-2 years |
We continue to be committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated QA Inspector, QA. In this role, you will be responsible for monitoring in-process product quality for Filling and Inspection and Packaging of parenteral products. The QA Inspector is responsible for performing visual and functional testing of product against statistically based sampling plans. In addition, the QA Inspector performs routine inspection and testing of components in accordance with Standard Procedures and specifications as required by production scheduling. In performing the above duties, the individual is responsible for accurately and clearly documenting test results in accordance with cGMPs. This position participates in rotation for weekend coverage and as needed during the work week. | 08/19/2025 |
| 706 | Hologic Newark, DE Electrical Engineer 3 Bachelor’s or Master's degree Exp: 0-3 years |
The Electrical Engineer 3 designs, develops, modifies and evaluates components and processes used in the generation, manipulation, transmission and storage of electricity. Determines design approaches and parameters. Analyzes equipment to establish operating data, conducts experimental tests and evaluates results. Selects components and equipment based on analysis of specifications and reliability. Completes documentation and procedures for installation and maintenance. May interact with users to define system requirements and/or necessary modifications. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise. A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is a fully qualified, career-oriented, journey-level position. Normally receives little instruction on day-to-day work, general instructions on new assignments. | 08/19/2025 |
| 707 | Hologic Newark, DE Sr. Quality Assurance Engineer Master’s Degree in Electrical Engineering Exp: 1-3 years |
Are you a quality-focused professional passionate about ensuring excellence in manufacturing and production processes? Join Hologic as a Senior Quality Assurance Engineer and play a critical role in designing, implementing, and maintaining quality assurance protocols that meet internal and external regulatory standards for worldwide distribution. In this role, you’ll collaborate with cross-functional teams, lead quality initiatives, and drive continuous improvement to ensure the delivery of high-quality, innovative products that improve lives globally. | 08/19/2025 |
| 708 | Humacyte Durham, NC 2D Bioprocessing Associate I Bachelor’s degree Exp: 0-1 years |
The Bioprocessing Associate I participates in the hands-on production of Humacyte’s regenerative vessels. | 08/19/2025 |
| 709 | Hyperfine Guilford, CT Regulatory Affairs Associate Bachelor’s or Master'sdegree in a scientific or regulatory discipline Exp: 6 months-1 year |
As our Regulatory Affairs Associate, you will be an individual contributor responsible for analysis, evaluation, preparation, and submission of documentation for regulatory approval, ensuring Hyperfine products and procedures comply with US and global regulatory specifications. You will support our Regulatory team across different program areas, and will work on multiple projects concurrently. | 08/19/2025 |
| 710 | ICON Wilmington, NC Staff Scientist - Drug Metabolism and Biotherapeutics (DMB) Bachelor’s degree in biology, Life Science, or related discipline Exp: 0-3 years |
As a Staff Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The Staff Scientist in Drug Metabolism and Biotherapeutics (DMB) will support research projects by helping plan and carry out in vivo pharmacokinetics studies. In this role, you’ll prepare doses, coordinate study schedules, and handle general lab tasks. You’ll also have the opportunity to cross-train and gain experience with in vitro assay support. | 08/19/2025 |
| 711 | ICON Wilmington, NC Chemical Library Specialist BS in Chemistry/Life Sciences or related field Exp: 0-3 years |
As a Chemical Library Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. In this role, you will contribute to the development and expansion of our internal high-throughput screening chemical library, supporting the discovery of new therapeutic entities. This position offers an exciting opportunity to apply your chemistry expertise in a dynamic laboratory environment. The successful candidate will play a key role in a variety of departmental initiatives and laboratory-based tasks, gaining hands-on experience in cutting-edge discovery chemistry projects. | 08/19/2025 |
| 712 | Illumina San Diego, CA Facilities Engineer 2 Master’s degree in Industrial Engineering, Mechanical Engineering, Electrical Engineering Exp: No exp |
The Facilities Engineer 2 will be part of the San Diego Facilities Engineering team. This role will be responsible for providing technical expertise as related to mechanical and electrical systems within facilities equipment engineering, support maintenance, and/or calibration and equipment performance optimization. Including projects related to mechanical, electrical, and plumbing (MEP) systems in an FDA regulated environment. The individual will possess technical knowledge of facilities water purification (RO/DI) skids, HVAC, chillers, centralized gas distribution systems, walk-in cold storage units, clean rooms, BMS/EMS system, Electrical generation and distribution system for Low, Medium and High Voltage, and other plant utilities, facilities validation, as well as construction management skills. | 08/19/2025 |
| 713 | Illumina Remote, OR Field Service Engineer 1 Bachelor’s degree in Electrical/Electronics Engineering, Mechanical Engineering, or a related field Exp: 1-3 years |
The Field Service Engineer plays a critical role in delivering exceptional on-site technical support for Illumina’s cutting-edge products. This position serves as a key liaison between customers and internal teams, ensuring optimal performance and satisfaction through expert service and support. | 08/19/2025 |
| 714 | Immunai New York, NY Associate Scientist, Molecular Profiling BS degree in Biology or related field Exp: 1-2 years |
The successful candidate will work in a fast-paced team alongside highly experienced scientists and will interface closely with a multidisciplinary team of immunology, molecular biology, and bioinformatics scientists. Specifically, they will contribute to the Molecular Profiling team performing high throughput profiling of clinical and experimental samples using flow cytometry, bulk RNA-seq, dissociated and spatial single cell multiomics. The successful candidate will be an excellent team player, agile in thought, energetic, and willing to learn new methods and skills. | 08/19/2025 |
| 715 | InBios International Seattle, WA Quality Engineer I (In Vitro Diagnostics) Master's degree in chemical, mechanical or bioengineering, or related discipline Exp: 1+ years |
As a Quality Engineer I, you’ll be instrumental in upholding the quality and compliance of our in vitro diagnostic products. You’ll collaborate with cross-functional teams to ensure our assays meet regulatory standards, perform reliably, and are safe for clinical use. Your strong organizational and communication skills will help foster a culture of quality and continuous improvement across the organization. | 08/19/2025 |
| 716 | INCOG BioPharma Fishers, IN Manufacturing Specialist - Formulation BS in biological sciences/biotechnology or related field Exp: 1 year |
INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in the formulation of sterile drug products. The Manufacturing Specialist (Formulation) is a key role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics formulation. The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 08/19/2025 |
| 717 | INCOG BioPharma Fishers, IN Manufacturing Specialist- Filling BS in biological sciences/biotechnology Exp: 1 year |
INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation. The Manufacturing Specialist is a key technical role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, or within highly regulated industries. | 08/19/2025 |
| 718 | Indee Labs Berkeley, CA Scientist, Immunology Masters Exp: 1-3 years |
We are seeking a Scientist or Senior Scientist, Immunology to join the team full time to accelerate the biological development of Hydropore at our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 08/19/2025 |
| 719 | Indee Labs Berkeley, CA Senior Bioengineer Masters Exp: 1-3 years |
We are seeking a Bioengineer or Senior Bioengineer, Immunology to join the team full time to accelerate the biological development of Hydropore at our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 08/19/2025 |
| 720 | Indee Labs Berkeley, CA MEMS Engineer Masters Exp: 1-3 years |
We are seeking an MEMS Engineer or Senior MEMS Engineer to join the team full time to accelerate the development of Hydropore in our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 08/19/2025 |
| 721 | Indica Labs Albuquerque, NM Field Applications Scientist Bachelor’s Degree in Biology or related biomedical science Exp: 1 year |
Hybrid sales and technical position which provides Applications Support and some Sales Support in digital pathology and image analysis for Indica Labs' HALO, HALO Link, and HALO AI platforms in a commercial, educational, or research environment. | 08/19/2025 |
| 722 | Indivior Raleigh, NC MQA Specialist Bachelor’s degree in science, engineering field, or equivalent Exp: 1-3 years |
The Manufacturing Quality Assurance (MQA) Specialist is responsible for providing quality oversight to all manufacturing areas to ensure product quality and SOP/GMP compliance. The MQA Specialist will work closely with production personnel to complete in-process batch record review, resolve batch related issues, and ensure proper good documentation practices. In addition, the MQA Specialist will be responsible for performing routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 08/19/2025 |
| 723 | Insmed Bridgewater, NJ QA Product Quality Complaint Specialist BS in engineering, Life Science or related discipline Exp: 1-2 years |
Reporting to the Director, Product Quality Complaints, the Product Quality Complaint Associate, QA will play a key role in the complaint process. Specific areas of responsibility include: Ensure accurate and thorough complaint intake information, replacement need, trouble-shooting with complainant, patient follow-ups, product complaint investigations, tracking and trending of complaint data. The position is based in our Bridgewater, NJ HQ (onsite 3 days a week). | 08/19/2025 |
| 724 | DWK Life Sciences Rockwood, TN Mechanical Engineer Bachelor’s Degree in Mechanical or Materials Science & Engineering Exp: 1+ years |
Creative leader with an entrepreneurial vision to develop new and improved cutting-edge products/processes as required by current and future clients. Subject Matter Expert in applying Engineering Disciplines to effectively manage projects from ideation to completion. Will work in a fast-paced production environment and apply creative thinking to develop and design mechanical solutions to improve production efficiency and reduce scrap. | 08/13/2025 |
| 725 | Element Fort Wayne, IN Microbiologist Bachelor's or Masters Degree in Microbiology Exp: 1-2 years |
Element has an opportunity for a Microbiologist to join our growing team in Fort Wayne, IN. The primary responsibility of the Microbiologist is to support laboratory operations by conducting the relevant microbiological testing. | 08/13/2025 |
| 726 | Element Santa Fe Springs, CA Quality Specialist I Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or related field Exp: 0-2 years |
Element has a current opening for a Quality Specialist I to join our growing team in Santa Fe Springs, CA. The Quality Specialist I supports the Quality Assurance function by performing routine QA activities to ensure compliance with applicable regulatory requirements (e.g., FDA 21 CFR Part 11, 210/211, ISO 17025) and internal quality standards. This entry-level position assists with reviewing analytical data packages, monitoring compliance in laboratory activities, equipment and method qualifications review and approval, and document control. Reports to the Quality Supervisor and/or Quality Manager. | 08/13/2025 |
| 727 | Element Wixom, MI Corrosion Technician Bachelor's degree Exp: 1-2 years |
Element has an opportunity for a Test Technician (Corrosion) to join our rapidly expanding team in Wixom, MI. Primary responsibilities include a variety of routine and non-routine testing assignments to assist the Corrosion Testing department. The technician must insure timely and accurate test results with minimal direct supervision. | 08/13/2025 |
| 728 | EMD Electronics Tempe, AZ Senior Research Chemist Master’s Degree in Physics, Chemistry, or other science discipline Exp: 1+ years |
In this role you will work within the Analytical Technology group for the analysis and characterization of CMP slurries for the semiconductor fabrication industry. | 08/13/2025 |
| 729 | Endo Rochester, MI Chemist II Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 08/13/2025 |
| 730 | Enovis Austin, TX Promade Product Development Engineer - Upper Extremities Masters degree Exp: No Exp |
Manages a specific product or group of products from product definition and planning through production and release. Responsible for coordinating employee recruitment, selection and training, performance assessment, work assignments, salary, and recognition/disciplinary actions. Directs interfaces with central resource in design, process, manufacturing, test, quality, and marketing as the product(s) move to completion and distribution. Manages production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; redesign of devices; analysis of customer returns; and optimization of device production relative to cost constraints. Serves as adviser to sales force and customers on all matters concerned with designated products. Recommends product program development and/or enhancements as a result of customer and/or sales force feedback. | 08/13/2025 |
| 731 | Enplusone Biosciences Watertown, MA Research Associate - Synthesis Bachelor’s degree in Molecular Biology, Biochemistry or Chemistry Exp: 1 year |
Your primary role as a Research Associate on the Synthesis team at EnPlusOne is to support the enzymatic RNA synthesis platform. You will assist staff scientists in RNA synthesis, reaction screening, data analysis, buffer preparation, QAQC, and inventory. You will work on multiple internal projects and external collaborations. You will be expected to keep a well-documented lab notebook, stay highly organized, use good communication, and collaborate well with our awesome team. Successful candidates are self-starters who are endlessly curious, excited by research, and flexible in a fast-paced, constantly evolving field. | 08/13/2025 |
| 732 | Eurofins Andover, MA Particle Characterization Scientist BS in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry, Bioengineering, Biotechnology, Biology or equivalent Exp: 1+ years |
The incumbent will participate in the formulation and process development of biotherapeutics. This position will be responsible for performing particle characterization of candidate molecules by using various biophysical, biochemical and particulates characterization techniques as well as supporting laboratory operations and maintenance. This is a laboratory-based position performing formulation and process development activities specifically for biotherapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. Furthermore, this position will assist in data compilation, data presentations, report authoring, and department documentation support. | 08/13/2025 |
| 733 | Eurofins Lancaster, PA Associate Scientist, Biochemistry Bachelor's degree in chemistry or other related degree concentration Exp: Entry level |
Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, aerosols, liquids, creams, and gels). Run the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus. Preparing samples for analysis and running some instrumentation with minimum supervision. Set up and validate new analytical or related processes used by the department. Prepare standards and samples for analysis. Execute method transfer protocols. Document work as required for GMP compliance. Perform monthly maintenance of laboratory equipment | 08/13/2025 |
| 734 | Eurofins Boston, MA Analytical Chemist M.S. in Analytical Chemistry, Biochemistry, Chemistry, or a related field Exp: 1 year |
This role supports analytical method development and data generation to inform product development, with cross-functional collaboration and a strong emphasis on scientific rigor, safety, and continuous improvement. | 08/13/2025 |
| 735 | Eurofins Malvern, PA Laboratory Operations Support (Project Management) BS/MS in a scientific field Exp: 1-5 years |
Initiate continuous improvement initiatives for Asset management and laboratory Operations and update impacted procedures. Maintain and support best business practices for Asset management such as Share Point Asset management. Work with managers, coordinators, and staff of labs to resolve instrumentation documentation issues. Work with QA and compliance to initiate, investigate, and resolve quality issues. Review QA’s monthly overdue work order list and research instrument service history and use to resolve documentation issues. Review training documents to see which are coming due for their 3-year update. Verify CAR-T data for regulatory submission and make SharePoint updates. Verify regulatory submission needed, and make Share Point updates. Facilitate change control closure and send out notifications to activity owners and approvers. Make status updates to change control SharePoint. Work directly with vendors to resolve instrumentation accuracy and inventory documentation issues. Support inventory accuracy for laboratories in Malvern and Spring House sites. Update Maximo/eCMMS to address inventory inaccuracies, and maintain eCMMS system’s accuracy. Provide process improvement and instruction to decrease turn-around time for bringing instruments into service. Research asset history for resolution of outstanding work orders. | 08/13/2025 |
| 736 | Eurofins Tustin, CA Chemist I - GCMS (Multiple Shifts) Eurofins Environment Testing BS or BA in chemistry or related field Exp: 1+ years |
Eurofins Environment Testing Southwest- Tustin CA is searching for a SVOA GCMS Chemist I to prepare and analyze environmental samples following EPA protocols in adherence with Eurofins Quality Assurance programs and SOP’s. | 08/13/2025 |
| 737 | Eurofins Lexington, MA Upstream Development Engineer Bachelor’s degree in chemical engineering, biochemistry, engineering or related pharmaceutical science Exp: 0+ years |
The Upstream development engineer will work primarily with scientists/senior research associates or engineers in the upstream fed-batch culture process development team to design and optimize consistent cell culture processes that produce quality recombinant proteins through laboratory studies. Additionally, as a fundamental component related to cell culture process design and development, the process development team will also ensure that these processes are predicable, scalable, and controlled with multiple size of bioreactors (ambr15, ambr250 and bench-top scale bioreactors). The position is to support tech transfer of developed/locked cell culture processes to pilot team and CMOs. | 08/13/2025 |
| 738 | Eurofins St. Charles, MO Associate Scientist – Cell Culture B.A./B.S./M.A./M.S. Degree in the life science field Exp: 0-2 years |
Performs work in a laboratory setting, meeting the physical job requirements of a lab role. Prepares and manages inventory of buffers, reagents, media, semi-finished and finished goods. Maintains cell culture in a BSL2 laboratory, and adheres to cleanroom guidelines and aseptic technique, according to protocols. Adheres to department SOPs and documentation requirements, maintains accurate data management and reporting. Generates data by performing lab assays in Ion Channel Services and other business units as needed. Conducts production assays with recombinant, primary and traditional cell models used in human tissues to cells and cell-based bioassays. Understands and complies with requirements for work performed at a GxP site. Completes required training and supports 100% of Employee Health and Safety requirements. Demonstrates proficiency with, care, and maintenance of lab equipment and department assets. Conducts responsible use of confidential IT and business systems, as required. Supports unit goals and demonstrates Eurofins’ competencies, as defined in the job plan. Provides training to colleagues and external end users, when required. Contributes to scientific community, and site research and development objectives. Works effectively in a team environment, under minimum direction, to achieve business production, project timelines, and quality objectives. Adjusts work hours and provides cross-functional support to other departments, as required, and maintains accountability in delivering to client needs/timelines. Routinely communicates project updates to internal and external clients. Performs other duties, as assigned. | 08/13/2025 |
| 739 | EvolveImmune Branford, CT Senior Research Associate, Immunobiology Master’s degree in Immunology or a related field Exp: 1-3 years |
We are seeking a creative and technically strong immunology-focused discovery scientist to join our Immunobiology team. The ideal candidate will have expertise in T cell engager biologic functional assessment, including tumor killing, cytokine production, T cell exhaustion assays, and multiparameter flow cytometry immune cell analysis. Experience in T cell engager discovery, particularly in evaluating CD3 bispecifics or costimulatory biologics, is preferred. The successful candidate will contribute to the discovery and assessment of novel costimulatory T cell engagers to determine key differentiation design features and supporting mechanisms of action. This includes designing and performing functional assays to prioritize alternative protein designs based on tumor killing potency, cytokine release and immune modulation mechanism of action. Collaboratively design in vivo proof of principle studies to test in vitro-driven hypothesis on molecule prioritization, mechanism of action, lead assessment, and selection of preclinical models to evaluate immune pharmacodynamic and establish in vivo mechanisms of differentiation. They will also work closely with our biotherapeutics and in vivo pharmacology research teams to drive T cell engager platform discoveries to drug development programs. Strong verbal and written communication skills are necessary, as is a proven track record of scientific and project achievements in biopharma. We are looking for a candidate who thrives in a collaborative, team-oriented environment and is eager to leverage the growth opportunities within a matrixed organization. This is an exceptional opportunity for a scientist passionate about T cell engager platform discovery and driven to translate innovative research into novel therapeutics. | 08/13/2025 |
| 740 | Evonik Birmingham, AL Plant Engineer I BS/MS in an engineering field including but not limited to Mechanical, Electrical, Industrial, Chemical, or Biomedical Engineering Exp: 1-3 years |
The Plant Engineer I acts as system owner and subject matter expert (SME) for assigned area(s) to include but not limited to infrastructure, utilities, and process equipment. He/ She will ensure that the assigned systems are in a state of operational readiness by ensuring that preventive maintenance is carried out on time and in full, any issues are documented and investigated, corrective and preventive actions are implemented. He/ She provides technical expertise to maintain and continuously improve assigned areas to improve reliability, reduce downtime, minimize costs and ensure technical means for safe and high-quality operation. | 08/13/2025 |
| 741 | Exact Sciences Madison, WI Laboratory Service Technician IV Bachelor’s degree in Engineering, Technology, Molecular Biology, Electronics, or related field Exp: 1+ years |
The Laboratory Service Technician IV is responsible for the Instrument Services of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Technicians and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. The LST may work continuously with other technicians and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. | 08/13/2025 |
| 742 | Exact Sciences Phoenix, AZ Quality Control Associate I Bachelor’s degree in Clinical Laboratory Science or Medical Technology or in the chemical or biological sciences Exp: 1+ years |
The Clinical Laboratory Quality Control (QC) Associate (Tues - Sat and Sun - Thurs 10:00am - 6:30pm) performs and functions within the Technical Laboratory under the guided direction of the Supervisor, Clinical Laboratory Quality Control Lead, or designee. In this support position, the Clinical Laboratory QC Associate ensures daily QC operations are effective and efficient by coordinating with leadership to anticipate and resolve issues related to efficiencies in quality control, and laboratory processes. | 08/13/2025 |
| 743 | Exactech Gainesville, FL Continuous Improvement Engineer Bachelor’s Degree in a related field Exp: 1-3 years |
The Continuous Improvement Engineer will be responsible for developing and sustaining performance management systems, lean manufacturing practices, and continuous improvement initiatives across operations, fulfillment, and other departments as needed. This role will focus on optimizing workflow, improving material and information flow, and implementing standardized work at all levels. The Industrial Engineer will play a key role in fostering a culture of continuous improvement (CI) and data-driven decision-making within the organization, ensuring compliance with ISO 13485 and other relevant regulations. | 08/13/2025 |
| 744 | Exactech Gainesville, FL Manufacturing Engineer Bachelor's degree Exp: 1-3 years |
Create and maintain the lowest cost, highest quality machining & manufacturing processes, tooling and supporting documentation for all parts produced. | 08/13/2025 |
| 745 | Exelixis Alameda, CA Scientist III, Discovery Oncology MS/MA degree in related discipline Exp: 1 year |
The successful and highly motivated candidate will work to identify the mechanism(s) of action of small molecular agents in cellular systems, evaluate the activity of small molecules in cell-based assays for oncology drug discovery, and help to enable new technologies for drug discovery efforts in cell models. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will actively contribute to develop cell-based functional assays and problem resolving, reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet deadlines. | 08/13/2025 |
| 746 | Fagron Wichita, KS QC Technician - Chemist I Bachelor’s degree in a science field Exp: 0-2 years |
The Quality Control Technician supports the Quality Control department by assisting with analytical testing, mainly for product release. | 08/13/2025 |
| 747 | Flamma Group Malvern, PA Associate Process Scientist BS or MS in Organic Chemistry Exp: 0-1 years |
Execute laboratory experiments. Assist in determining operational space for various process parameters to ensure efficient and successful scale up. Help evaluate safety of processes utilizing calorimetry data and stability data to fully understand the hazards and the trigger points of these hazards. Follow guidance from senior scientists or project leader to problem solve complex synthetic problems during development. Assist in scale up of processes in the kilo labs. Support scale up of processes in the pilot plant in a GMP environment. Collaborate with analytical chemists to complete work assignments. Contribute to laboratory organization (daily weigh checks, update of lab supplies inventory, lab supply purchase, lab cleaning, equipment calibration). Accurately collect reliable data in the form of lab procedure or reports to be used for updates to customers or during drafting of production’s MBR. | 08/13/2025 |
| 748 | Fluke Everett, WA Test Engineer I Bachelor's degree in Electrical Engineering Exp: 0-2 years |
Do you thrive in a fast-paced environment? Are you a self-starter who finds ways to improve existing processes? We are looking for a dynamic Test Engineer I to join our Fluke Electronics team here in Everett, WA. As a Test Engineer I, you will be tasked with analyzing, developing, implementing, and maintaining methods, manufacturing operation sequences, specifications, and equipment requirements for the production assembly of new and existing products. You will assist with new product introductions to manufacturing and provide ongoing product support. Through these activities, you will improve metrics in areas such as safety, quality, cost, and productivity. | 08/13/2025 |
| 749 | Fresenius Kabi Wilson, NC Scientist I B.S. in Chemistry, Biology or related physical science Exp: 1-4 years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 08/13/2025 |
| 750 | Frontage Laboratories Hayward, CA Research Assistant BS or MS in biology, chemistry, or related area Exp: 0-2 years |
This position will support experiment design, data collection, analysis, troubleshooting, and data reporting within the DMPK department. This includes gathering data on pre-clinical compound parameters using a variety of techniques, organizing and processing the data using statistical and analytical methods to reach meaningful conclusions, and reporting observations to clients and other decision-makers. | 08/13/2025 |
| 751 | Frontage Laboratories Exton, PA Scientist Genomics Bachelor’s or Master’s degree in Molecular Biology, Genetics, Biotechnology, or a related field Exp: 0-2 years |
We are seeking a detail-oriented and highly collaborative Scientist to join our Genomics team. This is an excellent opportunity for an early-career scientist to gain hands-on experience in a fast-paced environment supporting a wide range of client-driven studies. The successful candidate will have a solid foundation in molecular biology techniques such as PCR and nucleic acid handling, and excels in documentation, communication, and collaborative work. | 08/13/2025 |
| 752 | Frontage Laboratories Chicago, IL Research Technician BS degree in animal/veterinary science, biology, or related disciplines Exp: 0-3 years |
The Associate/Assistant Toxicologist plays a key, hands on role in the conduct of preclinical studies and supports the Study Director to ensure that Sponsor studies are conducted properly and according to FDA guidelines. | 08/13/2025 |
| 753 | Frontage Laboratories Concord, OH Associate Scientist I Bachelor’s degree in biology, microbiology, toxicology, chemistry, or a related scientific field Exp: 0-2 years |
We are seeking a motivated, detail-oriented individuals to join our GLP-compliant Genetic Toxicology Laboratory in Concord, OH. This full-time, on-site Associate Scientist-I role involves supporting in vitro and in vivo genetic toxicology assays, including bacterial reverse mutation assay (Ames Assay), in vitro Micronucleus Assay using using human lymphoblastoid (TK6) cell line and human peripheral blood lymphocyte (HPBL), and rodents in vivo Micronucleus assay, Comet Assay, and Pig-a assay. The successful candidate will be properly trained to perform hands-on laboratory procedures following study protocols, SOPs, and regulatory standards, contributing directly to data quality and compliance. | 08/13/2025 |
| 754 | FUJIFILM Biotechnologies College Station, TX Manufacturing Technician III, Solution Prep Bachelor’s degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or other related field Exp: 1 year |
The Manufacturing Technician III will work directly with a range of technologies. Dependent upon assignment, the range of technologies exposed to will be: Preparation of medium from stock raw materials including the compounding, mixing, testing and filtration for further process needs. Preparation of buffers from stock raw materials including the compounding, mixing, testing and filtration for further process needs. Weighing of raw materials per batch record specifications and assignment of appropriate expiry per procedures. Integrity testing of filters. Write and review standard operating procedures, buffer formulation records and batch production records. Assist senior staff in implementing project safety and quality assurance programs in accordance with SOPs. Maintain the confidentiality of proprietary company information. Document and maintain activity records according to cGMP regulations and ensure junior team members are trained. Operate general production equipment such as Autoclaves, Glass washers, Incubators, Analytical Scales, pH/conductivity meters, etc. Perform daily cleaning and sanitization of the laboratory and manufacturing areas. Maintain an effective working relationship with others. Perform all other duties as assigned. | 08/13/2025 |
| 755 | FUJIFILM Electronic Materials Mesa, AZ New Product Introduction Engineer - Pilot Plant BS degree in Chemical or Mechanical Engineering Exp: 0-2 years |
The Pilot Plant Lab Engineer supports process development and the production of low-volume products. Key responsibilities include performing SAP transactions, contributing to CIP projects, conducting Engineering Reviews, and managing equipment. Additionally, the role involves collaborating within the team and across departments to achieve project goals effectively. | 08/13/2025 |
| 756 | FUJIFILM Electronic Materials Mesa, AZ Quality Assurance Engineer Bachelor’s degree in Chemical Engineering, Chemistry, Industrial Engineering or Quality Engineering Exp: 1-2 years |
The Quality Assurance Engineer is responsible for executing and improving key QMS processes to drive improvements in FEUS processes and product quality, at a pace consistent with the needs of our strategic customers. | 08/13/2025 |
| 757 | FUJIFILM Biotechnologies Holly Springs, NC Sr. Analyst 1, QC Chemistry (Routine Testing) B.S. in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field Exp: 1-3 years |
The QC Chemistry Sr. Analyst 1 works with limited direction to execute QC analytical chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The QC Chemistry Sr. Analyst 1 adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory exceptions, invalid assays, deviations, change controls, and corrective and preventative actions (CAPAs). The role is primarily responsible for executing routine analytical methods in support of manufacturing, supporting laboratory execution of analytical method transfers and validations, and training other QC Chemistry laboratory associates. The ability to effectively communicate and function in a fast-paced, highly technical environment is essential to success. | 08/13/2025 |
| 758 | FUJIFILM Biotechnologies Holly Springs, NC Engineer / Scientist 2/3, Downstream - MSAT Master's degree in Engineering, Life Science or Chemical Engineering Exp: No exp |
The Engineer / Scientist 2/3, Downstream MSAT will provide tech transfer support and technical oversight for large scale purification activities for Monoclonal antibody production. | 08/13/2025 |
| 759 | Gameto New York City, NY Scientist I – Biomaterials Master’s degree in chemical engineering, biomedical engineering, materials science, chemistry, or a related field Exp: 1-2+ years |
In this position, you will serve as a key contributor to the design and optimization of bioengineered delivery platforms that form part of Gameto’s menopause implant program. Your work will directly support our mission to advance women’s health and contribute to Gameto’s core technology platform. We are looking for a self-motivated, technically skilled individual who enjoys working in a fast-paced, cross-disciplinary environment with evolving priorities. | 08/13/2025 |
| 760 | Genezen Lexington, MA MFG Specialist II - Compliance Master’s degree Exp: 1-2 years |
The MFG Specialist in this role will be part of a cohesive team responsible for Deviation investigations, CAPAs, and Change Controls for all phases of manufacturing. The Manufacturing Specialist uses expert knowledge of cGMP regulations and project management to ensure manufacturing readiness and compliance. The incumbent will also support equipment, documentation and process operations improvement initiatives within Manufacturing. The MFG Specialist works independently with minimal supervision and direction. Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion. | 08/13/2025 |
| 761 | Genezen Indianapolis, IN Microbiology Technician B.S. degree in a scientific/technical discipline Exp: 1+ years |
Microbiology Technician is responsible for Environmental Monitoring (EM) and Personnel Monitoring for pharmaceutical cleanrooms and the associated spaces including general microbiology laboratory responsibilities. The Environmental Monitoring (EM) technician ensures strict adherence to all cGMP/GMP policies and standard operating procedures and communicates effectively with other departments. The position requires working independently, but also under the supervision of the QC Microbiology management. This is a contract-to-hire position. As a contract employee, you will not be eligible for company benefits until you are converted to a full-time, regular employee. | 08/13/2025 |
| 762 | Genezen Lexington, MA QC Analyst - Microbiology (Contract) BA or BS in Microbiology or other related science Exp: 0-3 years |
The QC Analyst contract role will be responsible for routine and non-routine QC sampling and testing for the quality of products manufactured for our clients. QC is responsible for execution of the Environmental Monitoring (EM) program in place to monitor Genezen's controlled manufacturing environments (cleanrooms) as well as monitoring of utility systems including Water for Injection (WFI), Pure Steam, Purified Water, Compressed Air and Gas systems. These activities are all performed in accordance with cGMP guidelines and are supported by departmental and interdepartmental policies and standard operating procedures (SOPs). This position is based at Genezen’s state-of-the-art facility in Lexington, MA. This role supports daily operations as well as occasional weekend and holiday operations. This may include but is not limited to in-process monitoring and testing, lot release testing, and stability testing. Supporting activities for quality systems: utility monitoring excursions, non-conformance, deviations, corrective and preventive actions (CAPAs), investigations, Out of Specifications (OOS), and change controls may be required. | 08/13/2025 |
| 763 | GenScript Biotech Corporation Pennington, NJ Associate Scientist, Microbiology Bachelor’s degree in Microbiology, Biology, Biochemistry or related scientific field Exp: 0-2 years |
The position reports to the Manager of Microbiology, is ideally suited for a professional with technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to learn this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients. | 08/13/2025 |
| 764 | Celularity Morristown, NJ Operator, Clinical Manufacturing B.S degree in Biology, Bioengineering or related scientific discipline Exp: 1-2 years |
Celularity is seeking a dynamic individual to join a motivated team of clinical operators for the daily manufacture of multiple cell therapy products in support of clinical stage platforms and collaborations. Leveraging Celularity’s state-of-the-art cGMP capable facility, this position will make use of existing innovations and future technologies to meet and exceed manufacturing demand. | 08/05/2025 |
| 765 | Celularity Morristown, NJ Sr. Research Associate, Medical Devices, Research & Development B.S. in Bioengineering, Biology, or related discipline Exp: 1-3 years |
The Senior Research Associate is responsible for day-to-day analytical/biophysical testing and process development activities, supporting the company’s product development and commercial needs. This position will play a key role in the development and validation of innovative placenta-derived biomaterial medical devices or cell-based products, contribute to cross-functional R&D efforts driving regulatory submissions and operate at the interface of biomaterials, process development, product testing, and regulatory compliance to ensure robust product performance. This role involves developing and validating analytical/biophysical assays and testing product prototypes in compliance with regulatory requirements and industry standards. Furthermore, this role will conduct process development, validation, documentation and transfer to manufacturing activities relevant to medical devices, cell therapy or exosome products. | 08/05/2025 |
| 766 | CenExel Anaheim, CA Clinical Research Coordinator Bachelor's Degree Exp: 1+ years |
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. | 08/05/2025 |
| 767 | CenExel Garden Grove, CA Clinical Research Coordinator III Bachelor's Degree Exp: 1+ years |
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. | 08/05/2025 |
| 768 | Centogene Miami, FL Lab Technician (m/f/d) Bachelor’s degree in Molecular Biology, Genetics, Biomedical Science, or a related field Exp: 1-2 years |
Receive and verify biopsy samples from embryology labs. Perform DNA amplification, whole genome amplification (WGA), and library preparation for next-generation sequencing (NGS) in accordance with standard protocols. Operate and maintain lab equipment such as thermocyclers, centrifuges, and NGS platforms (e.g., Iontorrent; Illumina). Ensure accurate tracking of samples using laboratory information systems (LIS). Validate inputs, equipment and new protocols in accordance with the laboratory guidelines. Adhere strictly to laboratory quality control and quality assurance standards. Assist with data entry, documentation, and review of test results under supervision of clinical supervisors or geneticists. Maintain a sterile and compliant work environment following CLIA/CAP/ISO standards. Participate in validation and proficiency testing as required by accreditation bodies. Communicate effectively with embryologists, clinicians, and laboratory staff to ensure sample integrity and result accuracy. Present in front of customers, like a Scientific Advisor, attend conferences and write abstracts for those conferences | 08/05/2025 |
| 769 | Centrillion Palo Alto, CA Laboratory Technician B.A./B.S. in a molecular biology, genetics, or microbiology Exp: 6 months |
We are looking for a Laboratory Technician to join our R&D team in Palo Alto. The role is part of a small group that divides their focus between innovative new projects and product development. The ideal candidate will be extremely organized, familiar with basic laboratory techniques, and excited to learn and grow within the team. Technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. Candidates with knowledge and experience of PCR, library preparation, NGS sequencing or RNA seq will be given preference. | 08/05/2025 |
| 770 | Charles River Rockville, MD Biomanufacturing Associate II B.S. in biology/life sciences, bioengineering, or related discipline Exp: 1-2 years |
This role will apply solid knowledge and experience across a range of tasks, in resourceful and effective ways, requiring good judgment and initiative, when effectively executing manufacturing protocols. | 08/05/2025 |
| 771 | Charles River Wilmington, MA Laboratory Technician – MDX B.S. in biological sciences or related discipline Exp: 1 year |
Performs technical laboratory activities in support of client studies or procedures. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Reconciles customer paperwork with submission documentation to ensure accuracy. Makes detailed observations and maintains documentation of all laboratory work. | 08/05/2025 |
| 772 | Charles River Rockville, MD QC Micro Associate I – Environmental Monitoring B.S in Biology or related field Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Analyst I will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 08/05/2025 |
| 773 | Charles River Ashland, OH Senior Associate Scientist – Principal Investigator(Bioanalytical Chemistry) M.S./M.A. in a scientific related discipline Exp: 1-3 years |
Serve as a scientist in the conduct of assigned nonclinical research studies of basic complexity, to include study management, interpretation, and reporting of study data, and assuring the regulatory compliance of these projects. | 08/05/2025 |
| 774 | Charles River Mattawan, MI Senior Associate Scientist, Project Scientist – Large Molecule Bioanalysis Master’s degree Exp: 1-2 years |
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays, such as enzyme-linked immunosorbent assay, to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic assays to measure drug and Immunogenicity assay to measure anti-drug antibodies and neutralizing antibodies. Other assay types also performed are branched DNA and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery, Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 08/05/2025 |
| 775 | Charles River Cleveland, OH Research Analyst I - Manual Ion Channel Testing Bachelor’s degree (BA/BS) Exp: No exp |
The Manual Ion Channel Testing group is responsible for evaluating test article effects on ion channels in vitro. Personnel are responsible for operating and maintaining manual patch clamp electrophysiology workstations. Validated hardware and software systems are used to collect and analyze data under regulated (GLP) or non-regulated conditions. The group prepares, collects and transfers test article formulation samples to the CLE analytical chemistry unit (or other appropriate laboratory) for concentration verification and homogeneity analyses, and is responsible for interpretation and reporting of data outcomes. | 08/05/2025 |
| 776 | Charles River Cleveland, OH Research Analyst I – Bioanalytical Chemistry Bachelor’s degree (BA/BS) Exp: No exp |
Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 08/05/2025 |
| 777 | Cipla Hauppauge, NY QA Validation DHF - DPI Bachelor's degree in scientific discipline (e.g., biology, chemistry, pharmacy) or a related field Exp: 1-2 years |
Responsible for the coordination of supportive equipment and process validation activities such as testing, calibration, scale-up, engineering and validation studies, and assurance that the necessary project documentation is complete, accurate and in compliance with cGMP regulations. | 08/05/2025 |
| 778 | Cipla Fall River, MA Quality Assurance Analyst I Bachelor's or Masters degree in Chemistry. Pharmaceutical Sciences, or related field of study Exp: 1-3 years |
The Analytical Quality Assurance (AQA) associate I position is an team contributor role and reports to the Supervisor Analytical Quality Assurance for InvaGen Pharmaceuticals, Inc., a Cipla subsidiary located at Fall River, MA. | 08/05/2025 |
| 779 | Cipla Central Islip, NY QC Chemist I Master's degree in chemistry, pharmaceutical or related field Exp: 1+ years |
Demonstrated ability to perform independent work requiring attention to detail, accuracy and scientific judgment and a consistent record of shifting thought processes quickly from one task to another. Strong analytical skills, attention to detail, knowledge of analytical techniques (HPLC, GC, UV-Vis etc.) and familiarity with quality control procedures. Responsible for performing routine analytical testing of raw material, in-process samples, finished products to ensure they meet quality standards and regulatory requirements. Understanding of regulatory compliance, quality management systems and document control processes, and the ability to collaborate cross-functionally and communicate effectively. Perform activities related to periodic audit trail review of all quality softwares, ensure compliance within the systems etc. Maintaining regulatory compliance in accordance with cGMP and Perform Data Integrity risk assessment of current Good Manufacturing Practices (cGMP) and GLP systems both manual and automated. Follow all safety procedures and guidelines to ensure a safe laboratory environment. Prioritize risks and work with IT, QA, laboratory personnel to mitigate data integrity gaps. Partnering with other members of the Quality Assurance team and/or end users of the system to Identify, Develop, and Implement Continuous Improvements to the Change Control System, Process, and associated procedures. Evaluate proposed and existing software systems that support laboratory and software applications for data integrity gaps. Works with IT and QA to resolve those gaps. Develop standard operating procedures for the administration of analytical and QC equipment. Ensuring the GMP status and the functionality of the laboratory equipment in accordance with the guidelines 21 CRF Part 11 on data integrity. | 08/05/2025 |
| 780 | Confluent Medical Technologies Orange County, CA Process Development Engineer I BS degree in engineering Exp: 0-3 years |
We are looking for a Process Development Engineer I to join our Laguna Niguel, CA team. As a uniquely qualified candidate, you will: Responsible for process identification, parameter optimization, proof of concept testing, technology improvements, and process implementation. Responsible for tool, extrusion, and fixture design and qualification used for manufacturing medical devices and components. Must be able to accomplish broad and complex assignments. Capable of providing technical guidance to lower level personnel. Responsible for developing processing parameters for medical devices and components. Responsible for screening and optimization of process parameters to achieve robust and stable processes and maximize yields, efficiencies and process capabilities. Plans and conducts work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria. Design and perform Process Characterization Study’s & DOE’s, support protocols and reports. Have a firm understanding of validation strategy (IQ/OQ/PQ), support protocols and reports. Independently performs most assignments with instructions as to the general results expected. Perform data analysis to determine product performance and capability. Responsible for generating Work Instruction, Workmanship Standards, Engineering Memos and other related documents. Understand and execute Test Methods as well as develop inspection techniques for devices or components that cannot be measured using traditional methods. Works on problems and projects of moderate scope where analysis of situation or data requires a review of identifiable factors. Selects techniques to solve complex problems and make sound design recommendations. Exercises judgment within defined procedures and practices to determine appropriate action. Demonstrates full use and application of standard principles, theories, concepts and techniques. Selects design direction or modifications of components of systems. Work with project managers to create a project plan and timeline. Receives technical guidance on unusual or complex problems and supervisory approval on proposed plans for projects. Plans, schedules, conduct, and coordinates detailed phases of engineering work in part of a major project or in a total project of moderate scope. Performs work that involves conventional engineering practice but may include a variety of complex features such as conflic | 08/05/2025 |
| 781 | Contract Pharmacal Corp Hauppauge, NY Microbiologist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Microbiologist is responsible for and has experience in performing microbial analysis for the QC Microbiology laboratory which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 08/05/2025 |
| 782 | Cook Group Bloomington, IN Sterility Assurance Specialist Bachelor's degree in Engineering, Microbiology, Biology, or related field Exp: 1-2 years |
The Sterility Assurance Specialist I at Cook Incorporated is responsible for multiple projects/tasks related to ensuring continued compliance with sterilization validation and product adoption requirements. The Sterility Assurance Specialist will collaborate on cross-functional teams to perform necessary tasks relating to product/process change evaluations, sterilization validations, product adoption, and assurance of sterility requirements. | 08/05/2025 |
| 783 | Cook Group Bloomington, IN Senior Sustaining Engineer - Post Market Engineering Masters degree in Engineering or Engineering Technology or related discipline Exp: 1-2 years |
Senior Engineer, Sustaining, will perform activities related to sustaining commercially available products. These activities may include (but are not limited to) product/process remediation, risk analysis, regulatory approval support, and product/process improvements. The Senior Engineer works independently with limited supervision on complex activities and projects. The Senior Engineer acts as a mentor and leader in the department and may review/approve the work of less experienced engineers and/or contractors. | 08/05/2025 |
| 784 | CooperSurgical Houston, TX Quality Control Laboratory Technician I Bachelor’s degree in a related field Exp: 0-1 years |
The Laboratory Services Quality Technician I supports the Quality Control team by performing basic laboratory tasks, inspections, and documentation under close supervision. This entry-level role is responsible for assisting in routine quality control activities, maintaining lab cleanliness, and ensuring compliance with standard operating procedures. | 08/05/2025 |
| 785 | CooperSurgical Trumbull, CT Manufacturing Engineer I Bachelor’s degree in mechanical engineering, Industrial Engineering, or a related field Exp: 0-5 years |
The Manufacturing Engineer I at CooperSurgical is responsible for driving manufacturing excellence and optimizing production processes for our medical device and fertility products. The Manufacturing Engineer I plays a critical role in implementing lean principles, improving process efficiency, and fostering a culture of continuous improvement. | 08/05/2025 |
| 786 | Cardinal Health Mansfield, MA Post Market Vigilance Lab Support Engineer Bachelor's degree in related field Exp: 1-2 years |
CAH is currently seeking a Post market Vigilance Lab Support Engineer to join our Post market team located in Mansfield, MA (on-site). In this role, you will engage in all activities related to the CAH post market surveillance processes for returned samples. Your responsibilities will include processing returned samples and machinal testing of returned samples. | 08/05/2025 |
| 787 | Cardinal Health Mansfield, MA R&D Engineer Bachelor’s degree in mechanical engineering or a related field Exp: 0-3 years |
Under the direction of the Manager of R&D, this individual will be primarily supporting maintenance of business projects (MOB) with some potential support on New Product Development (NPD) projects. This position will have emphasis on executing against all requirements of a Design History File (DHF) including creating all product development documentation, protocols, and testing design requirements. The individual will work as a core team member supporting all aspects of the Change Development Process (CDP) as well as work with remote teams to execute on projects. This position will interact with other Research and Development groups, and Sales and Marketing, Manufacturing, Quality, Regulatory Affairs, Planning/Logistics, Packaging/Labeling and Outside Partners. | 08/05/2025 |
| 788 | Cresilon Brooklyn, NY Quality Assurance Technician B.S. in Engineering, Science, or Technology/Biotechnology Exp: 1 year |
The Quality Assurance Technician is responsible for routine inspection and testing of raw materials and components as well as of final product for Cresilon’s products in the Animal and Human Health industries. This position requires a strong attention to detail as the individual will be responsible for identifying deviations in product quality or safety and ensuring compliance with local, state, and federal regulations, including current Good Manufacturing Practices (cGMP). Position is for 2nd shift. | 08/05/2025 |
| 789 | Crown Bioscience San Diego, CA Research Associate I, In vivo Bachelor's degree Exp: 6 months |
The purpose of the In Vivo Research Associate I position is to provide support on In vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 08/05/2025 |
| 790 | CSL Chattanooga, TN Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 08/05/2025 |
| 791 | CSL Houston, TX Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 08/05/2025 |
| 792 | CSL Milwaukee, WI Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 08/05/2025 |
| 793 | Curia Rensselaer, NY Quality Investigations Specialist II MA/MS Degree in Biology or Chemistry or a a relevant field Exp: 1 year |
The Quality Investigation Specialist II plans and conducts activities concerned with the quality assurance of industrial processes, materials, and products. The role is responsible for overseeing and providing support for GMP investigations, internal audits, and customer complaint investigations. This role serves the Quality Assurance Department by implementing all procedures leading to compliant, valid, and documented release of drug, biologic product, or medical device by performing the following duties personally or through subordinate specialists. The Quality Assurance Specialist II participates in, writes and/or closes investigations. This requires maintaining budgetary targets and delivering earnings and growth to the company. | 08/05/2025 |
| 794 | Curia Albuquerque, NM Microbiologist I Bachelor’s degree in a scientific discipline, preferably microbiology or related field Exp: 1 year |
The Microbiologist I is responsible for performing microbiological testing and quality activities to support product production, environmental monitoring, and product release in a pharmaceutical manufacturing environment. This role ensures compliance with regulatory requirements and company standards by conducting microbiological assays, analyzing trends, and accurately documenting and reporting results. The QC Microbiologist I collaborates with cross-functional teams to identify potential microbiological risks, troubleshoot deviations, and contribute to continuous improvement initiatives to maintain product quality and patient safety. | 08/05/2025 |
| 795 | Curia Albuquerque, NM QC Analyst I Bachelor’s degree in Chemistry or related field Exp: 0-3 years |
The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications. | 08/05/2025 |
| 796 | Curia Rensselaer, NY QC Analyst I Bachelor’s degree in Chemistry or related field Exp: 0-3 years |
The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications. | 08/05/2025 |
| 797 | Curium Maryland Heights, MO Quality Control Technician Bachelor Degree in life science or a related field Exp: 1+ years |
Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP's and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management/Supervision that presents potential negative impact to manufactured or marketed product. | 08/05/2025 |
| 798 | Davita Deland, FL Assistant II, Laboratory Bachelor’s Degree Biological Sciences Exp: 0-2 years |
The Assistant II, Lab performs specimen accessioning, data entry, processing and other non-technical duties in the laboratory under the general supervision of the Supervisor. This position reports to Supervisor or Manager of Chemistry. This position does not require a registry license and may be non-technical; may be assigned to work a designated shift on day/evening/night. This position reports to the Manager, Laboratory (Lab). | 08/05/2025 |
| 799 | Dexcom San Diego, CA QA Engineer 2 Masters degree in a technical discipline Exp: 0-2 years |
This functional department provides technical support and guidance to product teams to ensure conformance to product development process and other applicable safety and quality system regulation and standards (e.g. IEC 62304, ISO 13485, ISO 14971). We are responsible for various aspects of Design Assurance with focus on product improvement, new product development and defect prevention. We interface with different cross functional groups (Product HW/SW Engineering, Software Test, Regulatory Affairs, Marketing, Project managers, Systems Engineering and others). We work closely with cross functional teams to establish and ensure compliance and quality for product related risk management documentation. Perform risk assessments and evaluations for products that conform to established standards and agency regulations. | 08/05/2025 |
| 800 | Dexcom San Diego, CA R&D Mechanical Engineer Masters degree in a technical discipline Exp: 0-2 years |
As an R&D Mechanical Engineer 2, you will be in a high visibility, high impact role both driving the design, development and implementation of new products, as well as providing ongoing support for existing on-market products. You will lead cross-functional discussions as the R&D Mechanical Engineering representative to ensure product quality, reliability, and performance while proactively driving continuous improvement efforts. | 08/05/2025 |
| 801 | Diacarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science Exp: 0-1 years |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 08/05/2025 |
| 802 | Diacarta Pleasanton, CA Research Associate I, In vivo BS or MS degree in molecular biology or a related field Exp: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 08/05/2025 |
| 803 | Diacarta Pleasanton, CA Manufacturing Technician B.S. degree in Molecular Biology, Cell Biology, Biotechnology or related field Exp: 1 year |
This position is a member of a fast-paced production team and will be responsible for the following tasks. Purchase raw materials from a vendor. Receive incoming materials and perform inspection and inventory recording. Production of DiaCarta IVD products to meet sales demands. Labeling of raw materials and finished goods. Perform calibration or preventative maintenance of the instrument. Participate in process improvement projects. Compliance with corporate quality systems. Other on-the-job assignments indicated by management. | 08/05/2025 |
| 804 | Bristol Myers Squibb Indianapolis, IN Associate Scientist I, Microbiology Bachelor’s degree in biology, Microbiology, or other Life Science related field Exp: 0-1 YEARS |
RayzeBio, a Bristol Myers Squibb company, is seeking applicants for an Associate Scientist, I for the Microbiology department. Reporting to the Manager of Microbiology, this role will help support the contamination control and sterility assurance testing activities at the manufacturing facility in Indianapolis. This role will conduct environmental monitoring and microbiological release testing of aseptically produced targeted alpha therapy (TAT) radiopharmaceuticals for RayzeBio’s clinical and commercial programs. | 07/30/2025 |
| 805 | Bristol Myers Squibb Summit West, NJ Manufacturing Associate, CAR T Media and Solution Preparation Bachelor’s degree Exp: No exp |
Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. | 07/30/2025 |
| 806 | Bristol Myers Squibb Devens, MA Associate, QC Analytical, Cell Therapy Bachelor's degree preferred in science Exp: 0-2+ years |
The Associate, QC Analytical, Cell Therapy is responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts. | 07/30/2025 |
| 807 | Bristol Myers Squibb Summit West, NJ Manufacturing Associate, Cell Therapy Bachelor’s degree Exp: No exp |
Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. | 07/30/2025 |
| 808 | Bristol Myers Squibb Indianapolis, IN Associate Scientist II, Isotope Production Bachelors degree in Chemistry or related science Exp: 1-3 years |
Reporting to the Supervisor of Quality Control, the associate scientist will help support the establishment of a new Quality Control laboratory which supports RayzeBio’s Isotope Production process in Indianapolis. The associate scientist will be providing support for the qualification and validation of analytical and radiochemical equipment for the QC lab. This position will conduct inspections and testing of raw materials, in-process controls, and finished products, ensuring compliance with specifications and regulatory standards. Specifically, the associate scientist will support the manufacture release of isolated isotopes to support RayzeBio’s clinical programs. | 07/30/2025 |
| 809 | Bristol Myers Squibb Devens, MA Manufacturing Associate, Cell Therapy Bachelors in relevant science or engineering Exp: 0-2 years |
The Manufacturing Associate, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The incumbent must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind, with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. | 07/30/2025 |
| 810 | Bristol Myers Squibb Indianapolis, IN Sr. Associate Scientist I MS in chemistry or related field Exp: 1-5 years |
RayzeBio is seeking a Senior Quality Control Chemist I reporting to the Quality Control Supervisor. The position will be responsible to ensure the testing and analysis of RayzeBio’s radiopharamceuticals are analyzed to cGMP standards. The applicant will be also be responsible to mentor junior chemists, provide technical support and liaise to other functional units, and to maintain an appropriate laboratory safety culture. The position will be located at RayzeBio’s manufacturing plant, in Indianapolis, IN. | 07/30/2025 |
| 811 | BWXT Erwin, TN Quality Engineer 1 B.S. Degree Exp: 1 year |
Assist senior Quality Engineers to develop, implement, and audit Quality Assurance and Quality Control systems to assure compliance to customer requirements or national standards. Assist senior Quality Engineer(s) to maintain the quality of specific products. Assist in the performance of system evaluations to assure compliance with customer, regulatory, or internal specifications. Continually strive for improved quality standards that shall lower costs of products and processes at NFS. | 07/30/2025 |
| 812 | BWXT Erwin, TN AUKUS Engineer 2 M.S. Degree in Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 07/30/2025 |
| 813 | BWXT Erwin, TN Engineer 1 - Electrical & Instrumentation Eng Bachelor’s degree in Engineering Exp: No exp |
Responsible for routine engineering assignments applying standard engineering techniques, procedures, and criteria under guidance of a manager or experienced engineer. Assignments are designed to develop professional work knowledge and abilities. Works under close supervision. Manager screens assignments for unusual or difficult problems and selects techniques and procedures to be applied on non-routine work. | 07/30/2025 |
| 814 | BWXT Erwin, TN Engineer 1 - Engineering (PIPELINE) Bachelor’s degree in Engineering Exp: No exp |
Responsible for routine engineering assignments applying standard engineering techniques, procedures, and criteria under guidance of a manager or experienced engineer. Assignments are designed to develop professional work knowledge and abilities. Works under close supervision. Manager screens assignments for unusual or difficult problems and selects techniques and procedures to be applied on non-routine work. | 07/30/2025 |
| 815 | BWXT Erwin, TN Engineer 2 - Fuel Process Engineering M.S. Degree in Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 07/30/2025 |
| 816 | BWXT Erwin, TN Engineer 2- Fuel Dev & Variability Reduction M.S. Degree in Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 07/30/2025 |
| 817 | BWXT Erwin, TN Engineer 2 -- Design Engineering -- Mechanical M.S. Degree in Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 07/30/2025 |
| 818 | Cambrex Charles City, IA Project Engineer BS in Engineering or equivalent degree Exp: 1-3 years |
The Project Engineer performs general engineering duties for new installations and equipment, and modification of existing facilities and equipment. These duties are to be carried out with safety, efficiency and quality at the forefront. | 07/30/2025 |
| 819 | Cambrex Charles City, IA Process Engineer BS in Chemical Engineering Exp: 1-3 years |
The Process Engineer will be responsible for implementation of projects for the manufacture of APIs and bulk intermediates and other products from development through piloting and/or commercial production. | 07/30/2025 |
| 820 | Cambrex Waltham, MA Chemical Process Technician Bachelor’s Degree in Chemical Process Technology, Chemistry, or Chemical Engineering Exp: 1 year |
We are looking for candidates who have a passion for working in a fast-paced, dynamic environment. The ideal candidate will have an Associate’s or Bachelor’s Degree in Chemical Process Technology, Chemistry, Chemical Engineering, or equivalent with one or more years of relevant experience, or a High School or GED degree with 10 years experience. The candidate should enjoy working in the field with their hands. The candidate should be well versed in handling equipment related to chemical processing, including working with glassware, compression fittings, tubing, pumps, and laboratory operations such as following chemical process recipes. From time to time, the candidate will also support general facility operations, including cleaning, waste management, and organization of various areas of the facility. | 07/30/2025 |
| 821 | Cambrex Longmont, CO Associate Scientist, Manufacturing BS in chemistry or related field Exp: 0-3+ years |
The Associate Scientist, Manufacturing will work within a team to perform kilogram scale organic synthesis of pharmaceutical drug substance. The Associate Scientist will operate chemical manufacturing equipment and execute detailed written instructions from a batch record under Good Manufacturing Practice (cGMP) conditions. In addition, the Associate Scientist is responsible for maintaining the manufacturing suites for activities by properly setting up, breaking down, operating, and cleaning production equipment for both GMP and non-GMP drug substance manufacturing operations. An Associate Scientist in manufacturing will operate under and develop subject matter expertise in cGMP practices and Good Documentation practices (GDP) within the Quality Management System. | 07/30/2025 |
| 822 | Cambridge Isotope Laboratories Andover, MA Quality Control Analyst II (LC/MS) Master's degree in Chemistry or a related field Exp: 1-2 years |
The Quality Control (QC) Analyst II is responsible for conducting routine and non-routine analysis of GMP and ISO materials under general supervision and in accordance with standard operating procedures (SOPs). They compile data for documentation of test procedures and prepare reports. They also calibrate and maintain lab equipment. They are able to perform basic troubleshooting and maintenance independently. Occasional travel between sites may be required. | 07/30/2025 |
| 823 | Cambridge Isotope Laboratories Twewksbury, MA Analytical Chemist MS in Chemistry, or other relevant science degree Exp: 1+ years |
The Analytical Chemist (GMP/RP/ISO) is responsible for providing laboratory support by researching and developing methods and implementing new analytical techniques, to be used for batch release testing of existing and new products. This may include performing validations or verifications of methods to ensure they are suitable for use. They are also responsible for providing support for investigations of out of specification or out of trend results and troubleshooting other analytical issues. They compile data for trending, assessment, and presentation of results and prepare reports under GMP guidelines and Standard Operating Procedures (SOP’s). They will also perform analytical work including maintaining laboratory instruments and equipment. | 07/30/2025 |
| 824 | Candel Needham, MA Contract Research Associate – Virology MS in Virology, Biotechnology, or related field Exp: 1-3 years |
We are seeking a highly motivated and collaborative Research Associate with a strong foundation in virology to support the development of next-generation HSV-1 viral immunotherapy candidates. This individual will contribute to the enLIGHTEN™ Discovery Platform through hands-on experimental work, including viral vector testing, mammalian cell culture, and virology-specific assays. The ideal candidate will bring a passion for innovation and a desire to work in a fast-paced, cross-functional research environment. | 07/30/2025 |
| 825 | Caris Phoenix, AZ Clinical Engineering Technician Bachelor's or Master’s degree in a science field Exp: 1 year |
The Clinical Engineering Technician is responsible for the installation and maintenance of equipment within the clinical molecular lab. | 07/30/2025 |
| 826 | Carlsbad Technology San Diego, CA Quality Control Chemist BS or Master Degree in organic chemistry, physical organic chemistry or Life Sciences Exp: Entry Level |
This position is responsible for the operation of laboratory equipment and will perform tests independently once training has been completed. The successful Chemist will be able to establish a congenial relationship with other employees to maintain a pleasant work environment and must have strong organizational skills and time management skills. | 07/30/2025 |
| 827 | Caris Phoenix, AZ Molecular Technologist, Solid Tumor Bachelor’s degree in scientific field Exp: 1 year |
The Molecular Technologist – Solid Tumor is responsible for performing various high complexity molecular techniques that include but are not limited to nucleic acid extractions and next generation sequencing (NGS). This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 07/30/2025 |
| 828 | Castle Biosciences Inc. Phoenix, AZ Lab, Molecular Technologist (Derm) B.S. in a scientific discipline Exp: 1-2 years |
A typical day for a molecular technologist involves extracting and analyzing RNA samples using various molecular laboratory techniques. This includes RNA quantification, PCR, reagent quality control, and instrument maintenance, all while interpreting data to ensure the accuracy and reliability of results. The role requires proficiency in molecular techniques, maintaining optimal working conditions, and upholding stringent quality control measures. Collaborating with team members is also integral to supporting an efficient workflow and maintaining high standards within the laboratory. | 07/30/2025 |
| 829 | Catalent Kansas City, MO Analytics Associate Scientist II Bachelor's degree in related scientific field Exp: No exp |
Catalent Pharma Solutions in Kansas City, MO is hiring an Analytics Associate Scientist II. Under general supervision, the Associate Scientist II performs work that is varied in analytical development and that may be somewhat difficult in character. Some evaluation, originality or ingenuity is required at the Associate Scientist II level. This individual follows established protocols and work plans and may be assisted by laboratory technicians/assistants. | 07/30/2025 |
| 830 | Catalent Baltimore, MD Associate Scientist III, - Downstream M.S. Degree in Engineering or Life Science Exp: 1+ years |
The Process Development Department is responsible for upstream and downstream process development, pilot scale execution, and tech transfer of developed processes to GMP manufacturing. This individual performs collaboratively and productively as an Associate Scientist III Downstream Development and actively engages in process development within a dynamic project team. Displays strong technical knowledge, initiative, and scientific commitment and makes significant technical contributions within the Process Development Group. Maintains openness to understanding areas outside of the primary function in order to foster continuous improvement. | 07/30/2025 |
| 831 | Catalent Kansas City, MO Associate, Quality Assurance Bachelor’s degree in a scientific field Exp: No exp |
The Associate, Quality Assurance (QA) is responsible for quality oversight of manufacturing “floor” activities and the associated in-process GMP (Good Manufacturing Practices) records. In addition to day-to-day responsibilities, the QA Associate will identify and participate in opportunities to improve processes. | 07/30/2025 |
| 832 | Catalent Kansas City, MO Quality Control Associate Scientist II Bachelor's degree in related life science or physical science field required (Biology or Microbiology preferred) Exp: No exp |
The Catalent site in Kansas City, MO is hiring a Quality Control (QC) Associate Scientist II. The QC Associate Scientist II performs tasks from detailed instructions and established procedures. This person will learn and comply with site Standard Operating Procedures (SOPs), corporate policies, and Environmental Health and Safety requirements. You will use basic knowledge of the principles and concepts of Biology & Chemistry for testing purposes. We’re seeking a self-motivated, detail-oriented person who is able to make decisions and solve problems independently or in a team environment. | 07/30/2025 |
| 833 | Catalent Chelsea, MA Manufacturing Associate Bachelor’s Degree in Life Sciences or Engineering Exp: 1 year |
Catalent Pharma Solutions is hiring a Manufacturing Associate performs routine and complex operations for the GMP production of pharmaceutical products. This individual operates in accordance with environmental, health, safety, and cGMP guidelines. This individual is responsible for the hands-on execution of production activities as they relate to spray drying operations of manufactured products. | 07/30/2025 |
| 834 | Catalent Greenville, NC Sample Management Specialist I BA or BS degree in science Exp: No exp |
The Sample Management Specialist I performs various activities within Quality Control with primary focus on sample management from external customers or internal departments centered around stability, reference standards, DEA control substances and sample logistics. The Sample Management Specialist I follows all regulatory guidelines, cGMP guidelines, Environmental Health and Safety regulations as required by the job function. | 07/30/2025 |
| 835 | Catalent Morrisville, NC Quality Control Chemist II Master’s degree in scientific or engineering field Exp: 1+ years |
Catalent Pharma Solutions is Morrisville, NC is hiring a Quality Control Chemist II. The Quality Control Chemist II will independently perform work using a variety of methodology. Experience in a variety of analytical techniques and instrumentation is required. These may include compendial testing, identification techniques (i.e. FTIR), chromatography, among others. The Quality Control Chemist II will perform scientific analysis of data and draw reasonable conclusions, follow established methods and protocols, perform initial troubleshooting and investigations as needed, demonstrate leadership skills regarding guiding and training less experienced colleagues and comply with the company safety and operational requirements and procedures requirements. | 07/30/2025 |
| 836 | Celerion Lincoln, NE Scientist/ Associate Scientist of Laboratory Automation Bachelor's degree in science or engineering-related field Exp: 1 year |
Celerion is hiring a Scientist/ Associate Scientist of Laboratory Automation to join our Lincoln, NE Bioanalytical team. This role will work onsite daily with our Hamilton, Tecan and Sciclone instruments. In this role, you will perform research and/or development in collaboration with scientific teams and automated systems based on new and existing methodologies. This hands-on role focuses on programming and operating laboratory automation systems with the objective of becoming the subject matter expert for all laboratory automation technologies within our organization. | 07/30/2025 |
| 837 | Cellares Bridgewater, NJ Process Engineer (I, II, III) Bachelor’s or Master’s degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, or a related field Exp: 0-4 years |
We are seeking an innovative and highly motivated Process Engineer on our MSAT team who will contribute significantly to establishing our IDMO Smart Factories. This position is focused on supporting the development and implementation of automated cell therapy manufacturing processes. You will work closely with the Process Engineering Lead and other cross-functional teams to execute, develop, design, optimize, and validate processes to ensure efficient, high-quality, scalable manufacturing solutions. This is a multidisciplinary role & this individual will interface across many parts of the company (with customers, scientists, researchers, and engineers) to develop the best solutions possible. Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company grows. | 07/30/2025 |
| 838 | Cellares South SF, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree or diploma in a scientific or related field Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. | 07/30/2025 |
| 839 | Cellipont Bioservices Woodlands, TX EM Technician, I Bachelor's degree in Microbiology, Biology, or related field Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a EM Technician I, who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The EM Technician I is responsible for Environmental Monitoring sampling, analyzing, and reporting results, to support manufacturing. Works in a fast-paced environment supporting the quality control department of a CMDO for manufacturing of biologic bulk drug substance, sterile finished drug product, and fill/finish. | 07/30/2025 |
| 840 | Cellipont Bioservices Woodlands, TX Manufacturing I Bachelors Degree in Life Sciences Exp: 0-1+ years |
Cellipont Bioservices is growing, and we are looking for a Manufacturing Associate I who believe in the potential bridging client's discoveries to patient cures and who want to challenge the status quo and take Cellipont and its clients to the next level. The Manufacturing Associate I is an entry level role and will be responsible for assisting in the planning and timely execution of manufacturing operations for a cGMP-compliant state-of-the-art cell processing/clinical manufacturing facility with emphasis on primary cell isolation and cell culture in an aseptic processing environment. The Manufacturing Associate I is responsible for following the standard practices outlined for the operation of the facility in accordance with the regulatory requirements for the manufacture of materials for our clinical studies, clinical trials and products. | 07/30/2025 |
| 841 | Cellipont Bioservices Woodlands, TX QA Technician I, Operations Bachelor's Degree Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician I, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician I, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician I, Operations is responsible for providing Quality Assurance support real-time for GMP Manufacturing of Cell Therapies. This individual will be responsible for providing QA on the Floor during manufacturing including observing critical processes, review executed GMP documentation, and supporting other QA functions as needed. | 07/30/2025 |
| 842 | Cellipont Bioservices Woodlands, TX QA Technician II, Operations Bachelor's Degree Exp: 1-2 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician II, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician II, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician II, Operations is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks. This individual will be responsible for providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. | 07/30/2025 |
| 843 | Cellipont Bioservices Woodlands, TX QC Analyst I, Analytical Bachelors Degree preferred in Life Sciences discipline Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a QC Analyst I, Analytical who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QC Analyst I, Analytical will work in a fast-paced environment supporting the quality control department of a CDMO for manufacturing of cell therapies. The QC Analyst I, Analytical will be responsible for routine testing, assay transfer and assay validation, QC document preparation and revision (SOPs/Protocols/Reports), as well as support for laboratory setup and maintenance. The QC Analyst I, Analytical, will also be responsible for ensuring all activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will also require the individual to demonstrate a strong ability to work cross-functionally and possess strong leadership skills. | 07/30/2025 |
| 844 | Bausch + Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 07/24/2025 |
| 845 | Bayer Ankeny, IA Research and Development Specialist II Bachelor’s or master’s degree in biology, Chemistry, Engineering, or other life science fields Exp: 1 year |
This Production Genotyping position (Research and Development Specialist II – 2nd Shift: Monday through Thursday, 3:00 pm to 2:00 am) is responsible for collaborating with laboratory team members to ensure timely delivery of high-quality data. The role requires achieving and surpassing daily and weekly production Key Performance Indicator targets, ensuring strict adherence to safety and compliance policies, identifying and executing experiments that drive process and system improvements, as well as operating and maintaining automation equipment. | 07/24/2025 |
| 846 | Beckman Coulter Diagnostics Miami, FL Manufacturing/Process Engineer II Master’s degree in Engineering in mechanical, electrical, and industrial Exp: 0+ years |
The Manufacturing/Process Engineer II for Beckman Coulter Diagnostics is responsible for providing day to day technical support and driving complex root cause investigations, for the instrument manufacturing product lines, including the assembly and final test processes, to drive quality and on-time delivery for our customers. This position is part of the Manufacturing Operation located in Miami, Florida and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Engineering Team and report to the Manufacturing Engineering Manager responsible for providing technical support to the manufacturing lines of Beckman Coulter’s premier Diagnostics products. If you thrive in a challenging, cross-functional, and fast-paced role and want to work to help build a world-class manufacturing organization—read on. | 07/24/2025 |
| 847 | Beckman Coulter Diagnostics Chaska, MN Manufacturing Engineer II Master’s degree in engineering field Exp: 0-2 years |
The Manufacturing Engineer II at Beckman Coulter Diagnostics is responsible for providing support and solving problems in the manufacturing process, from assembly to final packaging, across multiple instrument value streams. This role emphasizes driving continuous improvement initiatives to enhance efficiency, quality, and productivity. Additionally, the Manufacturing Engineer II will be accountable for leading efforts in design transfer efforts to meet business objectives. You will work cross-functionally to drive business results, DBS culture, and executing on strategic plans to achieve long term objectives. This position is part of the Hardware Operations located in Chaska, MN and will be an on-site position. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Technical Operations Team and report to the Engineering Manager responsible for Hardware Manufacturing. If you thrive in a fast paced, high visibility role and want to work to build a world-class manufacturing organization—read on. | 07/24/2025 |
| 848 | Beckman Coulter Diagnostics Chaska, MN Development Scientist I Bachelor's Degree in Life Science (Chemistry, Biology, Microbiology Biology or related science) Exp: 0+ years |
The Development Scientist I is responsible for responsible for participating in development and commercialization of immunoassays for an automated system. This person will assist in executing and analyzing experimental data as well as provide and presenting conclusions with team members as needed. They will participate in characterization, verification and validation of new and modified product designs. Additionally, you will be responsible for documentation of studies performed, including materials, methods, and conclusions. | 07/24/2025 |
| 849 | BD Franklin Lakes, NJ R&D Engineer II Bachelors Degree in Mechanical Engineering Exp: 1-5+ years |
The R&D Engineer II will be a key contributor on a R&D team within Medication Delivery Solutions, Injection Systems. The individual in this position will have understanding and exposure to a wide application of technical principles, theories and concepts. The R&D Engineer II provides solutions that are imaginative, thorough and practical to a wide range of complex problems. | 07/24/2025 |
| 850 | Bifrost Berkeley, CA Mechanical Engineer BS or MS in Mechanical Engineering or a related field Exp: 0-4 years |
Are you passionate about pushing the limits of technology to advance our understanding of the life sciences? So are we! We’re looking for a highly motivated and experienced Mechanical Engineer to join a fast-paced start-up developing tools that will transform functional cell biology research. The ideal candidate will have strong engineering and problem-solving skills, a solid grasp of mechanical design fundamentals and some exposure to optical systems, microscopy and bio-engineering or biology. As Mechanical Engineer, you will be part of a small team designing, developing, specifying and testing Bifrost’s hardware products. Additionally, you will play a role in product definition, development and verification testing. | 07/24/2025 |
| 851 | BioMérieux Salt Lake City, UT Manufacturing Engineer II Master’s degree in engineering or related discipline Exp: 1-3 years |
This engineer works on a cross-functional Manufacturing Engineering team to support several aspects of the consumable manufacturing process. Partners with internal team members and vendors to optimize product performance. Performs troubleshooting and routine maintenance of basic to moderate manual and automated manufacturing processes. Leverages experience and skillset to implement best practices within the realm of consumable medical device manufacturing by identifying root causes and recommending solutions. Contributes to the resolution of basic to moderate manufacturing engineering problems. | 07/24/2025 |
| 852 | BioMérieux Salt Lake City, UT Reagent Technical Project Manager III Bachelor’s degree in life sciences or Engineering Exp: 2 years |
The Technical Project Manager is assigned to projects within Reagent Manufacturing. This individual will collaborate with various leaders within manufacturing including operations, engineering, continuous improvement and other subject matter experts to create project documentation and implement projects on schedule as well as within accordance with design control and QMS requirements. In addition to meeting regularly with assigned project resources, this individual is also expected to provide regular project updates to leaders and stakeholders within the organization. | 07/24/2025 |
| 853 | BioMérieux Durham, NC QC Analyst 2-Night Shift Master's Degree in Biology, Chemistry or Biochemistry Exp: 0 years |
This position is in a fast-paced, FDA regulated environment in the Medical Devices/Diagnostics Industry. The QC Biochemistry Analyst 2 will be in a key position in the Biochemistry laboratory performing testing of Description, pH, FTIR, Osmolality, Moisture Analysis, Solubility, Loss on Drying, Resin Ratio, Reflectance, and pO2 Headspace Analysis, HPLC. | 07/24/2025 |
| 854 | BioMérieux Salt Lake City, UT Production Coordinator I (C Shift, Nights) Bachelor’s degree in a Biology/Chemistry or Supply Chain Exp: 1 year |
The Production Coordinator organizes and prepares work within a manufacturing group. Follows a production schedule to coordinate and organize resources necessary for production work orders and to ensure production flows smoothly and efficiently. Creates production batch records, prints/prepares labels, and gathers assigned materials lots for production orders. Participates in cycle counts, delivery of QC samples, and delivery/transaction of R&D materials. Ensures comprehensive compliance for proper documentation of batch records and material requirements for the production staff. Interfaces between production departments and with production schedulers, materials management, QA, and R&D to properly prepare the production orders per schedule requirements. Communicates any potential scheduling issues to the affected groups, and works with the production schedulers and scheduling manager to resolve scheduling issues. Monitors inventory status of production sub-assemblies critical to the manufacturing process, and communicates potential shortages to the production scheduler. Collects, reviews, and inputs data into databases. Normally receives general instruction on routine work and detailed instruction on new assignments. The Production Coordinator may participate in process improvements and other documentation efforts. | 07/24/2025 |
| 855 | BioMérieux Salt Lake City, UT Production Coordinator I (A Shift) Bachelor’s degree in a Biology/Chemistry or Supply Chain Exp: 1 year |
The Production Coordinator organizes and prepares work within a manufacturing group. Follows a production schedule to coordinate and organize resources necessary for production work orders and to ensure production flows smoothly and efficiently. Creates production batch records, prints/prepares labels, and gathers assigned materials lots for production orders. Participates in cycle counts, delivery of QC samples, and delivery/transaction of R&D materials. Ensures comprehensive compliance for proper documentation of batch records and material requirements for the production staff. Interfaces between production departments and with production schedulers, materials management, QA, and R&D to properly prepare the production orders per schedule requirements. Communicates any potential scheduling issues to the affected groups, and works with the production schedulers and scheduling manager to resolve scheduling issues. Monitors inventory status of production sub-assemblies critical to the manufacturing process, and communicates potential shortages to the production scheduler. Collects, reviews, and inputs data into databases. Normally receives general instruction on routine work and detailed instruction on new assignments. The Production Coordinator may participate in process improvements and other documentation efforts. | 07/24/2025 |
| 856 | BioMérieux Salt Lake City, UT BioReagents Formulator (C Shift) Bachelor’s degree with an emphasis on a biological science Exp: 1+ years |
Responsible for manufacturing products efficiently, accurately, safely and on time. Operates manufacturing equipment and in-process instrumentation to manufacture regulated products in accordance to QSRs, company policy and safety regulations. Works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Position requires attention to detail and fine motor dexterity. Relies on instructions and pre-established guidelines to perform the functions of the job and requires direct supervision or oversight by a senior employee. Works under immediate supervision of the BFDX Formulation Team Lead and reports to the BFDX Reagent Production Supervisor. | 07/24/2025 |
| 857 | Biogen Research Triangle Park, NC Manufacturing Associate III Bachelor’s Degree (STEM preferred) Exp: 6 months |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in;MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). | 07/24/2025 |
| 858 | Biogen Research Triangle Park, NC Engineer II, Automation B. S. in Engineering in Automation, Electrical, Chemical, Mechanical Engineering, or a similar Engineering discipline Exp: 0-2 years |
As part of our Automation & MES team, the Engineer II, Automation plays a pivotal role in supporting Biogen's RTP Bio site's operational and project goals. This position primarily focuses on maintaining and troubleshooting process control system hardware and software, including DeltaV DCS and Syncade MES, for biopharmaceutical manufacturing. You'll be responsible for creating software design specifications, implementing new control strategies, authoring recipes, and developing software test protocols for new products and processes. Additionally, you'll perform Responsible Engineering duties, such as reviewing validation protocols and creating Change Controls for system modifications. This role requires participation in an on-call rotation for troubleshooting and manufacturing support, managing small to medium engineering projects, and collaborating with cross-functional teams to drive improvements. Your work will directly contribute to optimizing our manufacturing operations and ensuring seamless production processes. | 07/24/2025 |
| 859 | BioLegend San Diego, CA Research Associate II - Cell Analysis Bachelor’s Degree in life sciences or Engineering Exp: 6+ months |
At BioLegend (a Revvity, Inc. company) we develop novel, cutting edge products and offer custom services to help with scientific innovation and discovery. We are currently looking for a talented, detail oriented person to join our growing Product Development team. The potential candidate will assist with development of new products for cell analysis such as antibodies, multi-color panels, and reagents for analysis of cell metabolism and cell imaging. The successful candidate must be a self-motivated, team player, able to communicate effectively with a multi-disciplinary team and must possess excellent organization skills. | 07/24/2025 |
| 860 | BioLegend San Diego, CA Biochemist I – GMP Bachelor’s degree Exp: 1 year |
The Biochemist I – GMP position will be responsible for the different stages of manufacturing various BioLegend’s regulated product produced in our US FDA registered cGMP manufacturing facility. This role will be responsible for formulating and vialing, completing batch records, putting away finished good inventory (FGI), data entry, equipment maintenance and supply inspections & storage. Other responsibilities include buffer preparation and inspection of incoming buffers into the GMP suite, as well as material preparation for Lyophilization and post lyophilization processes. This role will prepare product/project related documentation and maintain the device history records for all the regulated products and will work closely with product development on new products in order to establish a smooth transition into manufacturing. | 07/24/2025 |
| 861 | Biolog Newark, DE Lab Technician Bachelor’s degree in Life Science or related Exp: 0-3 years |
The Lab Technician supports Biolog’s Lab Services division by performing routine lab tasks that are essential to operations, such as sample handling and processing for ID, discards and restocking inventory. | 07/24/2025 |
| 862 | BioMarin Novato, CA Sr. Analyst, QC Critical Reagents Bachelor’s degree in a related field Exp: 1 year |
The QC Critical Reagents Associate / Sr. Analyst is accountable for maintaining all aspects of the BioMarin Critical Reagents program for commercial products in the global network, including but not limited to maintaining material inventory, generating technical documentation, and supplying materials to the global testing network. Materials in the Critical Reagents program include qualified reagents, reference standards, custom reagents, analytical cell banks and other important materials that require dedicated oversight. The individual prepares trend graphs and analyses for Critical Reagents to support routine requalification activities, regulatory responses, and investigational activities. | 07/24/2025 |
| 863 | Biomerics Winston-Salem, NC Quality Control Engineer, Associate Bachelor’s degree in Engineering Exp: 1-2 years |
The Associate Quality Control Engineer will support the Quality team by assisting with inspection and quality control activities. Learn to apply quality standards and procedures, follow guidelines to perform inspections, and help ensure products meet customer and internal requirements. Work closely with supervisors and production teams while gaining experience in quality methods and tools. | 07/24/2025 |
| 864 | Bio-Rad Irvine, CA Production Chemist I - Temporary Bachelor’s degree in a life science or related field Exp: 0-3 years |
Formulates products and intermediates utilizing biologicals and chemicals of varying properties and characteristics in order to meet specifications | 07/24/2025 |
| 865 | Bio-Techne Minneapolis, MN Scientific Support Associate Bachelor’s degree in Biological Sciences, Biochemistry, or equivalent Exp: 0-2 years |
The responsibilities of this position (Scientific Support Associate, SSA) are to respond to incoming technical inquiries and basic complaints by providing technical assistance on Protein Simple brand instrumentation, software, and applications, with a focus on first-class customer experience. Additional responsibilities will include maintaining technical resources and continual training to stay current on technical information for old and new products. Perform additional duties as assigned. | 07/24/2025 |
| 866 | Bio-Techne Minneapolis, MN Research Associate Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 07/24/2025 |
| 867 | Bio-Techne Minneapolis, MN Quality Technician, Hematology Bachelor’s degree in biology, or related field Exp: 0-1 year |
This position will require setup, maintenance, basic troubleshooting, and operation of Hematology analyzers. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to set up and test product on all laboratory instruments and troubleshoot as necessary within 12 months of hire. This position will adhere to safety regulations. Understand the basic ISO protocols and other applicable standards. Perform additional duties as assigned. | 07/24/2025 |
| 868 | Bio-Techne Minneapolis, MN Research Associate, Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. | 07/24/2025 |
| 869 | Bio-Techne Devens, MA Manufacturing Chemist - Formulation BS or BA degree in Biology, Chemistry or related science discipline Exp: 1-3 years |
The primary responsibilities of the Manufacturing Chemist are to execute formulations and perform in-process testing on customer specific formulations using Good Laboratory Practices and cGMP. In this role you will execute formulation activities independently and under the direction of senior chemists. The Manufacturing Chemist will be responsible for identifying manufacturing issues and effectively communicating those issues to management. | 07/24/2025 |
| 870 | Bio-Techne San Marcos, CA Chemistry Associate Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 years |
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 07/24/2025 |
| 871 | Biospectra Bangor, PA Laboratory Systems Technician I Bachelor's degree in Science or related field Exp: 1-3 years |
This position is primarily responsible for reviewing product documentation and verifying laboratory testing. This is an ideal position for an individual with a background in science, laboratory testing in a cGMP/GLP environment, who has an eye for details and likes the idea of being quality assurance for quality control and in so doing assist BioSpectra in ensuring the efficient operation of the Laboratory Services department. | 07/24/2025 |
| 872 | BioStem Technologies Pompano Beach, FL Quality Assurance Associate Bachelor’s degree in Life Sciences, Biology, Biotechnology, or a related field Exp: 0-2 years |
The Quality Assurance Associate plays a key role in supporting daily QA operations within a regulated tissue banking manufacturing environment. This entry-level position is responsible for executing routine quality assurance tasks such as document review, controlled material inspections, logbook audits, and ensuring compliance with internal procedures and applicable regulatory requirements (e.g., 21 CFR 1271, AATB Standards). This is an excellent opportunity for individuals looking to start a career in quality assurance, regulatory compliance, or biotech manufacturing. The QA Associate works closely with experienced QA staff and cross-functional departments to ensure high standards of quality and regulatory adherence are maintained throughout tissue processing operations. | 07/24/2025 |
| 873 | BlueSphere Pittsburgh, PA Cell Therapy Operator/Res. Associate Bachelor’s or Master’s degree in a cell biology, bioengineering, or medical technology-related field, or equivalent Exp: 0-5 years |
The Development team is looking for a motivated team member to join the fast-paced group and contribute to the process and analytical activities to take our TCR products into clinical production. We are looking for someone interested and eager to learn cutting-edge technologies and assist in the tech transfer and production of the products. | 07/24/2025 |
| 874 | Boehringer Ingelheim Gainesville, GA Technician III, Quality Control Bachelor’s Degree Exp: 1-2 years |
To perform, maintain and train on analytical techniques and methods for Quality Control testing required for product release. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. | 07/24/2025 |
| 875 | Bora Pharmaceuticals Baltimore, MA Analyst I, QC Microbiology - 3rd Shift BS in Microbiology/Biology or related field Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. This position supports our 3rd-shift, working 10pm-6:30am, Monday through Friday. | 07/24/2025 |
| 876 | Bora Pharmaceuticals Baltimore, MA Analyst I, QC Analytical-2nd Shift B.S. in Chemistry or related field Exp: 0-2 years |
Perform analytical testing per cGMP in support of raw material, in-process, final product, stability. Typical hours are 10:00 pm – 6:30 am, Monday through Friday. Hours may vary to meet business and training needs. | 07/24/2025 |
| 877 | BostonGene Waltham, MA Laboratory Project Coordinator Bachelor’s degree (B.S.) in biology, Molecular Biology, Biochemistry or related discipline Exp: 1-3 years |
The Project Coordinator plays a critical role in supporting laboratory collaborations with a focus on biospecimen management, regulatory compliance, and data integrity. This position ensures seamless sample handling and documentation for collaboration projects while contributing to system development in alignment with Good Clinical Laboratory Practice (GCLP) standards. | 07/24/2025 |
| 878 | BostonGene Waltham, MA Laboratory Technician, Biospeciman Services Bachelor’s degree in Biological or Life Sciences Exp: 1 year |
The Laboratory Technologist will be responsible for pre-analytical accessioning, processing, and maintaining inventory of clinical blood samples in accordance with established laboratory procedures. This role ensures the integrity of patient samples, supports downstream users in clinical and research operations, and maintains compliance with laboratory quality and regulatory standards. | 07/24/2025 |
| 879 | Bracco Medical Technologies Eden Prairie, MN Quality Systems Specialist II Bachelor’s degree Exp: 1-3 years |
The Quality System Specialist I is responsible for supporting the maintenance of the ACIST Quality Management System. The Quality Assurance Specialist will support the development of a robust quality system in compliance with all relevant standards and regulations at ACIST Medical Systems. | 07/24/2025 |
| 880 | Brainlab Houston, TX Biomedical Engineer (Clinical Specialist) B.S. in Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 years |
Provide on-site consulting and guidance to physicians and Operating Room (OR) personnel by evaluating options and problem-solving during surgery in order to maximize Brainlab product efficiency and usage. Manage and maintain install base, including basic 3rd Party integrations. Analyze and resolve product issues for Brainlab systems at assigned Account(s) via Salesforce through detailed analysis and utilization of critical thinking via technical training and documentation. Utilize engineering expertise to contribute to the quality improvement process by recommending product modifications. Provide clinical case coverage & support for. Complex Cases and Go Live launches (based on availability). Manage the process of driving customer utilization, especially via unique workflows and special applications. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of Image Guided Surgery (IGS) products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels and providing recommendations on this process. Work with the Application Consultant to increase revenue via the sale of spare parts, upgrades, contract renewal, etc. Work closely with the Application Consultant, Area Account Manager, and Marketing Manager on market transparency, upgrade initiatives, demo/evaluations, and Research & Development (R&D) projects. Attend meetings and trade shows to demonstrate and promote IGS products and services. Keep abreast of developments regarding Brainlab and competitive IGS products and services via ongoing training and individual research and analysis. Collaborate and strategize with Regional Support Manager to provide regular content for team calls/meetings (e.g. provide clinical knowledge transfer, share best practices, interesting cases or case set-ups, etc.). Maintain Salesforce documentation of all working hours. Attend IGS Continuing Education annually and maintain annual product certification competency | 07/24/2025 |
| 881 | Brainlab Hinsdale, IL Biomedical Engineer (Clinical Specialist) B.S. in Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 years |
Provide on-site consulting and guidance to physicians and Operating Room (OR) personnel by evaluating options and problem-solving during surgery in order to maximize Brainlab product efficiency and usage. Manage and maintain install base, including basic 3rd Party integrations. Analyze and resolve product issues for Brainlab systems at assigned Account(s) via Salesforce through detailed analysis and utilization of critical thinking via technical training and documentation. Utilize engineering expertise to contribute to the quality improvement process by recommending product modifications. Provide clinical case coverage & support for. Complex Cases and Go Live launches (based on availability). Manage the process of driving customer utilization, especially via unique workflows and special applications. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of Image Guided Surgery (IGS) products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels and providing recommendations on this process. Work with the Application Consultant to increase revenue via the sale of spare parts, upgrades, contract renewal, etc. Work closely with the Application Consultant, Area Account Manager, and Marketing Manager on market transparency, upgrade initiatives, demo/evaluations, and Research & Development (R&D) projects. Attend meetings and trade shows to demonstrate and promote IGS products and services. Keep abreast of developments regarding Brainlab and competitive IGS products and services via ongoing training and individual research and analysis. Collaborate and strategize with Regional Support Manager to provide regular content for team calls/meetings (e.g. provide clinical knowledge transfer, share best practices, interesting cases or case set-ups, etc.). Maintain Salesforce documentation of all working hours. Attend IGS Continuing Education annually and maintain annual product certification competency | 07/24/2025 |
| 882 | Brainlab Denver, CO Biomedical Engineer (Clinical Specialist) B.S. in Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 years |
Provide on-site consulting and guidance to physicians and Operating Room (OR) personnel by evaluating options and problem-solving during surgery in order to maximize Brainlab product efficiency and usage. Manage and maintain install base, including basic 3rd Party integrations. Analyze and resolve product issues for Brainlab systems at assigned Account(s) via Salesforce through detailed analysis and utilization of critical thinking via technical training and documentation. Utilize engineering expertise to contribute to the quality improvement process by recommending product modifications. Provide clinical case coverage & support for. Complex Cases and Go Live launches (based on availability). Manage the process of driving customer utilization, especially via unique workflows and special applications. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of Image Guided Surgery (IGS) products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels and providing recommendations on this process. Work with the Application Consultant to increase revenue via the sale of spare parts, upgrades, contract renewal, etc. Work closely with the Application Consultant, Area Account Manager, and Marketing Manager on market transparency, upgrade initiatives, demo/evaluations, and Research & Development (R&D) projects. Attend meetings and trade shows to demonstrate and promote IGS products and services. Keep abreast of developments regarding Brainlab and competitive IGS products and services via ongoing training and individual research and analysis. Collaborate and strategize with Regional Support Manager to provide regular content for team calls/meetings (e.g. provide clinical knowledge transfer, share best practices, interesting cases or case set-ups, etc.). Maintain Salesforce documentation of all working hours. Attend IGS Continuing Education annually and maintain annual product certification competency | 07/24/2025 |
| 883 | Brainlab Lynchburg, VA Biomedical Engineer (Clinical Specialist) B.S. in Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 years |
Provide on-site consulting and guidance to physicians and Operating Room (OR) personnel by evaluating options and problem-solving during surgery in order to maximize Brainlab product efficiency and usage. Manage and maintain install base, including basic 3rd Party integrations. Analyze and resolve product issues for Brainlab systems at assigned Account(s) via Salesforce through detailed analysis and utilization of critical thinking via technical training and documentation. Utilize engineering expertise to contribute to the quality improvement process by recommending product modifications. Provide clinical case coverage & support for. Complex Cases and Go Live launches (based on availability). Manage the process of driving customer utilization, especially via unique workflows and special applications. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of Image Guided Surgery (IGS) products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels and providing recommendations on this process. Work with the Application Consultant to increase revenue via the sale of spare parts, upgrades, contract renewal, etc. Work closely with the Application Consultant, Area Account Manager, and Marketing Manager on market transparency, upgrade initiatives, demo/evaluations, and Research & Development (R&D) projects. Attend meetings and trade shows to demonstrate and promote IGS products and services. Keep abreast of developments regarding Brainlab and competitive IGS products and services via ongoing training and individual research and analysis. Collaborate and strategize with Regional Support Manager to provide regular content for team calls/meetings (e.g. provide clinical knowledge transfer, share best practices, interesting cases or case set-ups, etc.). Maintain Salesforce documentation of all working hours. Attend IGS Continuing Education annually and maintain annual product certification competency | 07/24/2025 |
| 884 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Small Scale Synthesis B.S. Chemistry or Biochemistry degree Exp: 0-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Scientist to join the Discovery Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, purification, analytical chemistry, and contributing to specific program goals. The Associate Scientist will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 07/14/2025 |
| 885 | Arrowhead Pharmaceuticals Verona, WI Associate Manufacturing Scientist I BS or MS in chemistry, biochemistry, engineering, or related scientific field Exp: 0-5 years |
The Associate Manufacturing Scientist supports the production of drug substances and drug products. Their responsibility will focus on the preparation of solutions and reagents by following standard protocols. This technically focused position supports lab work, helps solve problems, and effectively communicates with colleagues. | 07/14/2025 |
| 886 | Arrowhead Pharmaceuticals Verona, WI Associate Scientist, Quality Control B.S. in Chemistry (or related field) Exp: 1-3 years |
This position is within the Quality Control structure under the Quality Department. An Associate Scientist I, Quality Control will support the analytical testing of pharmaceutical raw materials, in-process samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. The Associate Scientist I will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies. The Associate Scientist is expected to perform several analytical techniques and can make sound scientific decisions under guidance from management. This position reports to QC Laboratory Management. | 07/14/2025 |
| 887 | Artivion Kennesaw, GA Process Engineer Master's degree in Engineering (Mechanical, Chemical, Biomedical, Industrial or related field of engineering) Exp: 1-3 years |
Responsible for providing process engineering support for all product manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as develop new processes to improve manufacturing efficiency. Supports new product launches by collaborating with other functional areas and providing process engineering expertise during the implementation of processes or equipment. | 07/14/2025 |
| 888 | AskBio Durham, NC Quality Control Analyst I Bachelor’s degree in biology or related field Exp: 0-2 years |
The purpose of the Analyst I, Quality Control (Non-Clinical) is to perform analytical testing to support the release of Non-Clinical grade rAAV vector lots manufactured in various AskBio departments (including, Pre-Clinical Manufacturing, Process Development, MSAT) and external partners. The rAAV vectors tested/characterized by the team will support capsid technology development, intellectual property portfolio, and internal progression of early-stage gene therapy programs. | 07/14/2025 |
| 889 | Astellas Pharma Sanford, NC Specialist, QA Validation M.S. degree in Biological/Physical/Chemical sciences, engineering, or equivalent Exp: 1-3+ years |
The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing, Quality Control, Facilities, and Automation. | 07/14/2025 |
| 890 | Astellas Pharma South SF, CA Research Associate II, Discovery Bioscience Master's degree in a life science, chemical engineering or related discipline Exp: 1+ years |
The Research Associate will be an integral member of the Vector Bioscience team and assist in developing, characterizing, and producing AAV vectors. The Research Associate will work at our South San Francisco R&D laboratories, supporting and collaborating with various research and development groups. | 07/14/2025 |
| 891 | AstraZeneca Philadelphia, PA Automation Engineer BA/BS Engineering/Life Sciences Exp: 0-5+ years |
Are you ready to take on the challenge of crafting the future of automation in a multifaceted environment? As an Automation Engineer, you'll be at the forefront of technological advancements, providing technical mentorship and support for equipment at our Philadelphia and Bensalem sites. You'll play a pivotal role in the procurement of new equipment, leading projects and collaborating with IT, operations, facilities, and maintenance teams to implement changes. | 07/14/2025 |
| 892 | AstraZeneca Mount Vernon, IN PET Formulation Senior Process Engineer Master's degree required, preferably in Science, Chemical Engineering, or other related technical discipline. Exp: 1 year |
Are you ready to break new ground and leave a collective legacy? As a PET Formulation Senior Process Engineer, you will provide technical support for formulation, investigating and correcting process-related problems and deviations from standards. You will serve as a Subject Matter Expert for multiple processing operations and provide technical leadership within the Process Engineering team. You may also lead Technology Transfers to and from the site. | 07/14/2025 |
| 893 | August Bioservices Nashville, TN Manufacturing Technician II/III Bachelor's degree in biological, chemical sciences, or engineering Exp: 1+ years |
August Bioservices is seeking to hire experienced manufacturing technicians to support our growing formulations and filling teams. Headquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! | 07/14/2025 |
| 894 | August Bioservices Nashville, TN Microbiologist I B.A./ B.S in Biology (or related) Exp: 0-2 years |
August Bioservices is looking for a Quality Control team member that is passionate and driven professionally. August Bioservices desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. Reporting to the Manager, Microbiology, the Microbiologist I will be responsible for performing biological assays of raw materials, in-process samples, finished product, and environmental monitoring samples. He/she will work with microbiology personnel to assure test results, procedures, and methods are written, maintained, executed, and approved in accordance with approved SOPs and regulatory requirements. | 07/14/2025 |
| 895 | Avalign Akron, OH Quality Engineer BS in an engineering science Exp: 0-3 years |
The Quality Engineer is responsible for supporting the organization to ensure quality and production goals are met. The Quality Engineer will utilize an engineering approach to improve manufacturing efficiencies and ensure quality standards of all products are met. | 07/14/2025 |
| 896 | Avalign Greenwood, IN Quality Engineer BS in an engineering science Exp: 0-3 years |
The Quality Engineer is responsible for supporting the organization to ensure quality and production goals are met. The Quality Engineer will utilize an engineering approach to improve manufacturing efficiencies and ensure quality standards of all products are met. | 07/14/2025 |
| 897 | Avantor Carpinteria, CA Process Engineer II B.S. in engineering, chemical Exp: 1-3 years |
Avantor is looking for an engaging and motivated Process Engineer to optimize our NuSil team, delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of our Carpinteria, CA. You will have the opportunity to be responsible for all phases of medium-scale assigned process improvement projects, ensuring the successful conclusion of all phases within an appropriate time and at appropriate cost. If you are passionate about expanding your knowledge base and making a positive impact – let’s talk! | 07/14/2025 |
| 898 | Avantor Bakersfield, CA Process Engineer II B.S. in engineering, chemical Exp: 1-3 years |
Avantor is looking for an engaging and motivated Process Engineer to optimize our NuSil team, delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of our Bakersfield, CA facility with occasional travel to our sister site in Carpinteria, CA. You will have the opportunity to be responsible for all phases of medium-scale assigned process improvement projects, ensuring the successful conclusion of all phases within an appropriate time and at appropriate cost. If you are passionate about expanding your knowledge base and making a positive impact – let’s talk! | 07/14/2025 |
| 899 | Avantor Sant Louis, MO Quality Control Lab Analyst Bachelor’s degree in Biology, Chemistry, Biochemistry, or other science Exp: 0-3 years |
Perform microbiological assays including microbial limits testing, endotoxin testing, and environmental monitoring. Prepare and process raw material, in-process samples, and finished products for microbiological testing. Operate and maintain laboratory equipment such as autoclaves, incubators, laminar flow hoods, and microbial identification systems. Ensure equipment calibration is performed per established schedules. Conduct routine environmental monitoring of laboratory and production areas, including water and viable air monitoring. Maintain laboratory inventory and order consumables as needed. Maintain accurate records and ensure proper documentation of all laboratory activities, test results and events. | 07/14/2025 |
| 900 | Aviva Systems Biology San Diego, CA Research Associate I/II, Molecular Biology B.S. or M.S. in life science or related subject Exp: 1+ years |
Aviva Systems Biology is a fast paced, mid stage life sciences research tools company located in San Diego, CA. We commercialize life science tools and reagents for research, drug discovery, and diagnostics. Perform routine molecular biology techniques such as PCR, transfection, cell lysis. Perform small-scale bacterial, fungal, and mammalian cell culture using aseptic techniques. Operate incubator/shakers, centrifuges, and other laboratory equipment used in protein production. Use electrophoresis and chromatography systems for biomolecule analysis or purification. Prepare chemical solutions required for production processes. Analyze Sanger sequence data for validation of expression constructs | 07/14/2025 |
| 901 | Aviva Systems Biology San Diego, CA Research Associate I/II, Biochemistry B.S. or M.S. in life science or related subject Exp: 1+ years |
Aviva Systems Biology is a fast paced, mid stage life sciences research tools company located in San Diego, CA. We commercialize life science tools and reagents for research, drug discovery, and diagnostics. Perform routine biochemistry techniques such as protein expression, purification, and characterization by SDS-PAGE. Perform small-scale bacterial, fungal, and mammalian cell culture using aseptic techniques. Operate incubator/shakers, centrifuges, and other laboratory equipment used in protein production. Use electrophoresis and chromatography systems for biomolecule analysis or purification. Prepare chemical solutions required for production processes. Analyze Sanger sequence data for validation of expression constructs | 07/14/2025 |
| 902 | Axogen Vandalia, OH Quality Analyst - 1st Shift Bachelor’s Degree in a Life Science discipline, engineering, or in a related field Exp: 0-2 years |
The Quality Analyst performs quality control (QC) inspections and dispositions of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen’s Quality System. The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable with FDA, state OSHA and ISO regs and standards. Employees within this role will performs a variety of tasks under limited supervision. | 07/14/2025 |
| 903 | Axogen Vandalia, OH Quality Analyst - 2nd Shift Bachelor’s Degree in a Life Science discipline, engineering, or in a related field Exp: 0-2 years |
The Quality Analyst performs quality control (QC) inspections and dispositions of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen’s Quality System. The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable with FDA, state OSHA and ISO regs and standards. Employees within this role will performs a variety of tasks under limited supervision. | 07/14/2025 |
| 904 | Axogen Vandalia, OH Quality Analyst - 3rd Shift Bachelor’s Degree in a Life Science discipline, engineering, or in a related field Exp: 0-2 years |
The Quality Analyst performs quality control (QC) inspections and dispositions of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen’s Quality System. The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable with FDA, state OSHA and ISO regs and standards. Employees within this role will performs a variety of tasks under limited supervision. | 07/14/2025 |
| 905 | Axogen Tampa, FL Laboratory Technician, R&D Bachelor’s degree Exp: 1 year |
The Laboratory Technician plays a key role in supporting the daily operations of Axogen’s R&D laboratory. This position is responsible for executing routine experiments and testing, preparing and analyzing biological and tissue-based samples, and maintaining laboratory equipment and supplies. The Laboratory Technician will ensure safe handling and disposal of hazardous and biohazardous materials, maintain accurate records, and contribute to the continuous improvement of lab workflows. Success in this role requires strong attention to detail, a collaborative mindset, and the ability to work effectively in a regulated environment. | 07/14/2025 |
| 906 | B. Braun Irvine, CA QC Chemistry Assoc I Bachelor's Degree Exp: 0-2 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 07/14/2025 |
| 907 | B. Braun Daytona Beach, FL QC Lab Tech II-Chemistry Bachelor's degree Exp: 1-2 years |
Performs a variety of quality control tests on products at various stages of the production process to ensure compliance with quality and reliability standards. Records statistical data. Analyzes data and writes summaries to validate or show deviations from existing standards. Recommends modifications to existing or suggests new, standards, methods and procedures. | 07/14/2025 |
| 908 | B. Braun Daytona Beach, FL QC Lab Tech II-Microbiology Bachelor's degree Exp: 1-2 years |
Performs a variety of quality control tests on products at various stages of the production process to ensure compliance with quality and reliability standards. Records statistical data. Analyzes data and writes summaries to validate or show deviations from existing standards. Recommends modifications to existing or suggests new, standards, methods and procedures. | 07/14/2025 |
| 909 | BA sciences Salem, NH Sample Control Technician Bachelor’s degree in a scientific discipline Exp: 0-2 years |
The Sample Control Technician is responsible for ensuring that all samples are entered into the Laboratory Information Management System (LIMS) and made available to the lab staff in a timely manner. Assists with the coordination and maintenance of stability studies as directed and in accordance to FDA, cGMP, and Boston Analytical's Standard Operating Procedures. This position reports to the Manager of Sample Control. | 07/14/2025 |
| 910 | BA sciences Salem, NH Chemist II Bachelor’s degree in Chemistry or a related discipline Exp: 1+ years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 07/14/2025 |
| 911 | BA sciences Salem, NH Microbiologist I, MB BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 07/14/2025 |
| 912 | BA sciences Salem, NH Microbiologist I, VD BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist conducts validation and feasibility testing for quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 07/14/2025 |
| 913 | BA sciences Salem, NH Microbiologist QC I BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 07/14/2025 |
| 914 | Bachem Vista, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 07/14/2025 |
| 915 | Bachem Torrance, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 07/14/2025 |
| 916 | Balt Irvine, CA Quality Engineer I Bachelor’s degree in engineering or science discipline. Exp: 0-2 years |
This position is responsible for the implementation, maintenances, and sustainment of the Balt USA’s quality management system in accordance with procedures compliant with 21 CFR Part 820 and ISO 13485 requirements. Develops and analyzes quality systems procedures and documents by leveraging regulatory requirements and continuous improvement principles. Upholds compliance efforts for NCMR, CAPA, quality audits, procedure adherence, GMP enforcements and applies continuous improvement principles to support kaizen events, problem solving, fixturing improvement, and scrap reduction. Support efforts for supplier quality management and supplier development as part of nonconforming corrective action. Works with various employees to develop, improve, and stabilize quality process controls. Monitors quality issues to help determine root cause and implement corrective action. Works with all functions to achieve quality and business goals. Compiles and writes training material and conducts training sessions on quality control activities. | 07/14/2025 |
| 917 | Baxter Marion, NC Quality Lab Associate I - Endotoxin Master’s Degree in biological sciences Exp: 0-3 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 07/14/2025 |
| 918 | Baxter Round Lake, IL Senior Mechanical Engineer Master's degree in Mechanical Engineering or a related field Exp: 1+ years |
Are you ready to make a difference in the world of healthcare? Join our innovative team as aSenior Mechanical Engineer, where your creativity and technical expertise will help shape the future of our infusion system product portfolio. In this role, you will tackle exciting challenges, develop cutting-edge solutions, and contribute to life-saving technologies that have a real impact on patients' lives. If you’re passionate about engineering and eager to work in a dynamic environment, we want to hear from you! As a Senior Mechanical Engineer, you will be at the forefront of product development, working on both new and existing infusion systems. | 07/14/2025 |
| 919 | Baxter Round Lake, IL Quality Lab Associate I - 3rd Bachelors degree in Chemistry or Science related degree Exp: 6+ months |
The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. This is a 3rd shift position, Monday-Thursday, 10:00 pm - 8:30 am. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 07/14/2025 |
| 920 | Baxter Round Lake, IL Research Associate II - LC-MS Master's degree in relevant scientific discipline (chemistry, pharmaceutical sciences) Exp: 1+ years |
As a Research Associate you will effectively contribute to a variety of projects within the R&D team and development & validation of LC-MS methods targeting specifically nitrosamines. Conduct routine/non-routine research and design experiments. Participate in project team and work in collaboration with other R&D groups of Formulation Development, Quality Control, Process Development, Manufacturing, etc | 07/14/2025 |
| 921 | Baxter Hayward, CA Tech IV, MNF Formulation Bachelor’s degree Exp: 1 year |
The Manufacturing Technician IV is responsible for assisting the supervisor in organizing, scheduling and directing other team members as well as execute all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Manufacturing Technician IV may be the main interface with other functional departments to resolve issues. Represent the department in cross- functional team as necessary. | 07/14/2025 |
| 922 | Baxter Marion, NC Quality Lab Associate I - Environmental Monitoring B.S. degree in Microbiology, Biology, or related science Exp: 0-2 year |
Supports the environmental monitoring program by performing testing such as surface testing, viable air monitoring, and air total particle counts. Responsible for conducting routine risk assessments and HEPA filter inspections in cleanrooms. | 07/14/2025 |
| 923 | Baxter Round Lake, IL Quality Lab Associate I - 2nd Shift Bachelors degree in Chemistry or Science related degree Exp: 6+ months |
The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. This is a 2nd shift position, Sunday - Wednesday, 2:00 pm - 12:30 am. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 07/14/2025 |
| 924 | Aktis Oncology Boston, MA Sr/Clinical Trial Associate - Clinical Ops Bachelor’s degree in life sciences, healthcare, or related field Exp: 1-3 years |
The Clinical Trial Associate (CTA) will support the planning, execution, and documentation of clinical trials involving radiopharmaceutical agents. Working under the direction of the Clinical Trial Manager or Clinical Operations Lead, the CTA will assist with key trial activities including study start-up, tracking, document management, and coordination with external vendors and clinical sites. This role is critical for maintaining quality, compliance, and operational efficiency across clinical programs. | 07/09/2025 |
| 925 | Alamar Biosciences Fremont, CA Manufacturing Associate I B.S. or B.A. degree in Biology, Chemistry or equivalent Exp: 1+ years |
We are seeking a highly disciplined, energetic, and results-driven candidate to join our Operations team as Manufacturing Associate I. Manufacturing Associate I is responsible for executing production orders to meet daily production schedule under some supervision. Job responsibilities include the manufacturing of biological reagents and finished products such as reagent formulations, antibodies conjugation, components lyophilization, and filling and assembly of final products. Experience working under ISO 13485 and/or current Good Manufacturing Practice (cGMP) in a biotechnology or pharmaceutical industry is highly preferred. | 07/09/2025 |
| 926 | Alamar Biosciences Fremont, CA Manufacturing Associate I - Temporary B.S. or B.A. degree in Biology, Chemistry or equivalent Exp: 1+ years |
We are seeking a disciplined, energetic, and fast learning candidate to join our Operations team as Manufacturing Associate I. Manufacturing Associate I is responsible for completing production orders in accordance with the daily production schedule. Job responsibilities include the manufacturing of biological reagents and finished products such as reagent formulations, antibodies conjugation, components lyophilization, and filling and assembly of final products. Experience working under ISO 13485 and/or current Good Manufacturing Practice (cGMP) in a biotechnology or pharmaceutical industry is highly preferred. | 07/09/2025 |
| 927 | Alcami Wilmington, NC Scientist II - Chemistry Masters degree in Chemistry, Biochemistry, or related field Exp: 0+ years |
The Scientist II (Chemistry) is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, ICP, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing in addition to other key methodologies such as KF and titration. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) and may also assist with method development / method validation projects. | 07/09/2025 |
| 928 | Alcami Morrisville, NC Manufacturing Technician II - Sterile Injection (3rd Shift) Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician II (Compound/Fill/Finish) is accountable for results in a fast-paced environment and assists with the manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. The Manufacturing Tech II is a key role responsible for executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology. This position entails a high level of technical expertise in aseptic processes requiring single-use components, ability to troubleshoot, and responsibility for maintaining quality and compliance with Good Manufacturing Practices (GMP). The Manufacturing Tech. II performs the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Tech. II employs acceptable techniques while working in manufacturing environments, including PPE gowning. The candidate must have the ability to learn specific department procedures, have a general understanding of Good Documentation Practices (GDP) and GMP, and follow directions from leadership/peers to ensure manufacturing goals are met. | 07/09/2025 |
| 929 | Alcami Charleston, SC Pharmaceutical Manufacturing Technician - 3rd Shift Bachelor's degree in chemical engineering Exp: 1+ years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employ acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. | 07/09/2025 |
| 930 | Alcami Morrisville, NC Manufacturing Technician I - Sterile Injection (2nd Shift) Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician I (Compound/Fill/Finish) is accountable for results in a fast-paced environment and assists with the manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. The Manufacturing Tech I is a key role responsible for executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology. This position entails a high level of technical expertise in aseptic processes requiring single-use components, ability to troubleshoot, and responsibility for maintaining quality and compliance with Good Manufacturing Practices (GMP). The Manufacturing Technician I performs the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Tech. I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The candidate must have the ability to learn specific department procedures, have a general understanding of Good Documentation Practices (GDP) and GMP, and follow directions from leadership/peers to ensure manufacturing goals are met. | 07/09/2025 |
| 931 | Alcami Morrisville, NC Scientist II - Compendial Testing, Raw Material Master’s degree Exp: 0+ years |
The Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Scientist II / III may also be required to work on method development/method validation projects. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). | 07/09/2025 |
| 932 | Alcon Johns Creek, GA Sr. Associate M.S. Exp: 0+ years |
As a Senior Associate, you will lead research efforts focused on the development of next generation contact lenses and innovative materials for medical devices. This role requires a strong expertise in material science, especially in understanding the structure-property relationship of materials and demands an innovative mindset to drive research forward. | 07/09/2025 |
| 933 | Alcon Johns Creek, GA Sr. Associate, Automation and Control Engineering M.S. Exp: 0+ years |
s a Sr. Associate, Automation and Control Engineering, supporting our supporting our Engineering Manufacturing Systems team, you will be trusted to design, implement, install, analyze and/or optimize manufacturing processes, procedures, equipment, and programming. The ideal candidate will also have expertise in PLC and automation controls, ensuring seamless integration and functionality of mechatronic systems to best support our 24/7 operation at Johns Creek, GA. | 07/09/2025 |
| 934 | Alcon Johns Creek, GA Opto-Mechanical Engineer M.S. Exp: 0+ years |
As an Opto-Mechanical Engineer, you will collaborate with design engineers, metrology engineers, chemistry and process scientists, and clinicians, to deliver state-of-the-art opto-mechanical, mechanical and optical designs supporting new product development for ophthalmic medical device products. This role will be in located in Johns Creek, GA. The Opto-Mechanical Engineer designs, models, analyzes, and tests optical, electro-optical, and opto-mechanical systems and components, including sensors, lasers, fiber-optics, and telecommunications products. Conducts research and development into phases of physical optics and geometric optics, lasers, laser characteristics, laser maintenance, and broadband optical sources. Applies research of complex optical systems to achieve desired optical outcomes. Develops component specifications, tolerances, simulations and tests procedures for electro-optical systems and components. Uses design-to-cost models, six sigma methodology, and other methods to assure and verify optical design requirements are met. | 07/09/2025 |
| 935 | Aldevron Madison, WI Associate Scientist II - Upstream PD Bachelor's or Master's degree in biology, biotechnology, molecular biology, biochemistry, chemistry, or a closely related field Exp: 0-1+ years |
The Associate Scientist II position is part of the Upstream Process Development team in the Protein Business Unit of Aldevron. This is an on-site position at the facility located in Madison, WI. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Technical Operations team and report to the Upstream Process Development manager. Your responsibilities will revolve around developing processes to produce recombinant proteins using microbial host expression systems. | 07/09/2025 |
| 936 | Aldevron Fargo, ND Analyst I QC Environmental Monitoring Bachelor’s degree in microbiology or related scientific field Exp: 0-1 years |
The Analyst I Quality Control Environmental Monitoring is responsible for sampling, detecting, quantifying, and identifying possible contaminants that may interfere with the quality of the product during the different stages of the manufacturing process. This position reports to the QC Microbiology Supervisor and is part of the Quality Control Environmental Monitoring Team located in Fargo, ND and will be an on-site role. | 07/09/2025 |
| 937 | Alkermes Wilmington, OH Manufacturing Associate I-OSD Nights Bachelor's degree Exp: 0-1 years |
This entry-level position involves working with a small team in a GMP environment to manufacture commercial and/or clinical-scale batches. | 07/09/2025 |
| 938 | Alloy Therapeutics Waltham, MA Research Associate, Oligonucleotide Discovery B.S. or M.S. degree in Biology or related science Exp: 1-3 years |
As a Research Associate, you will work within the Genetic Medicines team in Waltham, MA. You will also collaborate with internal/external partners on nucleic acid drug discovery projects to ensure timely execution of the experiments, and delivery of high-quality data. This role will have an autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This role will report to Senior Scientist with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. | 07/09/2025 |
| 939 | Almac Souderton, PA Validation Officer - ENG Bachelor’s Degree Exp: 1 year |
Almac Group is currently seeking a Validation Officer for our Souderton, PA location. The Validation Officer will work as part of the Quality department, you will be responsible for coordinating validation activities, at any Almac Clinical Services site, to ensure that simple equipment, facilities, and processes (E/F/P) achieve compliance with business and regulatory requirements and to ensure their validated status is maintained throughout their operational lifetime. | 07/09/2025 |
| 940 | Almac Audubon, PA QC Inspector Grade 1 Bachelor’s Degree Exp: 1 year |
Almac is seeking a Quality Control Inspector Grade 1 for our Audubon, Pa. location. The Quality Control Inspector Grade 1 will be responsible for upholding the high standard of GMP within the business. The successful candidate will be expected to perform in process checks, environmental monitoring, sampling and testing of packaging components and medicinal bulk, and assessment of clean down and line clearances of production rooms and equipment. | 07/09/2025 |
| 941 | Altasciences Columbia, MO Scientist, LCMS /Bachelor’s degree in Immunology/ Biology/ Chemistry or equivalent discipline Exp: 6 months |
You will assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. You will also support and perform data collection activities including primarily focused on mass-spectrometry. | 07/09/2025 |
| 942 | Altasciences Everett, WA Pathology Associate I, II, III Bachelor of Science (B.S.) or Bachelor of Arts (B.A.) Exp: 6 months-1 year |
To provide high quality and timely processing of pathological specimens through gross examinations, necropsies, tissue trimming and tissue processing as specified in company protocols and SOPs. | 07/09/2025 |
| 943 | Altasciences Everett, WA Laboratory Supervisor Bachelor's degree in a scientific discipline. Exp: 1-3 years |
Responsible for managing Research Associates and assisting Scientists on studies/projects. Assists with training other laboratory staff in technical procedures. Assist with evaluating and optimizing the utilization of laboratory resources to attain operational goals, meet study deadlines, and deliver quality results. Works with Laboratory Sciences Senior Manager of Operations in formulating current and long-range plans, objectives and policies. | 07/09/2025 |
| 944 | Alveo Alameda, CA Scientist II BA/BS degree in Biochemistry, Molecular Biology, Microbiology or related field Exp: 1-4 years |
Alveo Technologies is looking for an Assay Development and Verification Scientist II to support ongoing Validation and Verification efforts for projects in disease detection. The Scientist will assist in planning and executing protocols and conducting experiments at the bench to meet objectives. This position will review, understand and follow the instructions, protocols and SOPs. | 07/09/2025 |
| 945 | American Regent Brea, CA Production Supervisor Bachelor’s in Pharmaceutical Science, Chemistry, [Micro] Biology, Engineering, or a related field Exp: 1-3 years |
This position is a member of the Manufacturing Team. The Manufacturing Team is responsible for activities associated with the manufacture of safe, effective, and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Manufacturing Team ensures aseptic and sanitary conditions are maintained where required, appropriate manufacturing area and equipment records are neat and accurate and safe, effective, and professional behavior is displayed at all times. In conjunction with Production Management the Manufacturing Team provides input and assistance to other Departments as needed, playing a critical role in maintaining production schedules and meeting Company goals. The Production Supervisor will be able to oversee all aspects of the Manufacturing Process. The Manufacturing Process includes component prep, aseptic cleaning, compounding, filtration, and filling in accordance with established production records in a concerted effort to manufacture sterile liquid pharmaceuticals. The Production Supervisor will be able to perform, oversee and provide signatory approval for all activities associated with the manufacturing process. The Production Supervisor will be able to provide direction, training and mentorship to all junior team members as needed. The Production Supervisor will be the responsible person for the proper use of batch documentation. The Production Supervisor will be able to troubleshoot most of the manufacturing process and equipment and where necessary make adjustments and minor repairs during setup and during operations. | 07/09/2025 |
| 946 | Amneal Brookhaven, NY Scientist, Quality Control Master Degree (MBA) Microbiology or related science discipline Exp: 1+ years |
Performs microbiological analysis of water, raw materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as aseptic techniques, plating techniques, dilution and enumersastion techniques adhering to company policies as identified in standard operating procedures (SOPs). Prepares samples for analysis involving aseptic techniques and proper sample handling techniques as applicable. Perform Identification of organisms. | 07/09/2025 |
| 947 | Amneal Piscataway, NJ Validation Engineer Bachelors Degree (BA/BS) BS: in Pharmaceutical manufacturing, Engineering, Science or relevant field Exp: 1 year |
The Validation Engineer is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes. | 07/09/2025 |
| 948 | AstraZeneca Waltham, MA Scientist, Bioscience BS in Biology, Biotechnology or other relevant area Exp: 1-2 years |
Discovery Sciences applies deep technical expertise in specialist technologies to support the delivery of targets and molecules to the early AstraZeneca pipeline. Targets are identified through our human genomics and functional genomics efforts, employing the latest technologies in genome editing and advanced cell model development. Once identified and validated, we work with therapy area project teams to identify novel small molecule effectors of these targets using our integrated sample management and platform screening groups. As the new range of targeted therapeutics moves towards the clinic, we are placing an increased emphasis on understanding the links between the chosen molecular target, disease type/stage, and drug responses. Key to this is the provision of high-quality cellular models for research. The GCB team is critical for delivering these cellular models and developing methods to prepare primary cell lines for projects aligned with our strategic objective of increasing the translatability of the cell models used in research. We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role of Scientist, GCB. | 07/09/2025 |
| 949 | Andelyn Biosciences Columbus, OH Environmental Monitoring Technician Bachelor’s degree, a background in the life sciences, biotechnology, or gene therapy industries Exp: No exp |
The Environmental Condition Team is responsible for the activities associated with the manufacture of safe, effective pharmaceuticals in accordance with company SOPs, and policies. The Environmental Monitoring Team works in concert with and assists the manufacturing department and plays a critical role in ensuring environmental control of the cleanroom. The Environmental Monitoring Technician position is primarily responsible for performing environmental monitoring activities including air, surface, and personnel monitoring within the cleanroom. In addition, to sampling critical utilities throughout the GMP facility.. | 07/09/2025 |
| 950 | Anika Bedford, MA QC Incoming Inspector I Bachelor’s degree Exp: 0-1 years |
The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture on the second shift. The position also performs inspection activities during in-process manufacturing for second shift. | 07/09/2025 |
| 951 | Anika Bedford, MA QC Microbiologist I BS in microbiology, biology or related science Exp: 1+ years |
Responsible for all microbiological and some analytical testing of production materials under GMP conditions. Responsible for process and equipment validation (autoclave and depyrognenation oven) in cooperation with Engineering and R&D (New Product Sterility and LAL validation.) | 07/09/2025 |
| 952 | Antheia Menlo Park, CA Downstream Process Engineer I B.S. in Chemical Engineering or relevant area of study Exp: 0-2 years |
Antheia is seeking a junior Process Engineer to join our Downstream Processing team. In this role, you will help develop and scale processes to separate and purify bio-derived Key Starting Materials and APIs, moving from bench to pilot and commercial scales. You will gain an understanding of how impurities behave, how products degrade over time, and how to design processes that stay within target cost and performance ranges. You will support day-to-day unit operations, collect and analyze data, and help define key parameters for each step. Hands-on lab skills in sample preparation, as well as experience with liquid-solid and liquid-liquid separations, are important. You’ll work closely with cross-functional teams—including Biology, Analytics, Operations, Quality, and Regulatory—to help create efficient, reliable processes that deliver high-quality products on schedule. | 07/09/2025 |
| 953 | Applied Medical Rancho Santa Margarita, CA Machine Design Engineer, Automation Bachlor's degree in Mechanical Engineering or in a related field Exp: 1 year |
Are you a visionary Design Engineer? Join Applied Medical and be at the forefront of revolutionizing medical device manufacturing. As part of our Automation team, you will be at our global U.S. headquarters, pioneering cutting-edge machines, collaborating across departments, and leading the way in cost reduction, optimizing manufacturing processes. As a Design Engineer, you will play a vital role in supporting the development of automated machines or automated processes for our in-house medical device manufacturing. It's your chance to make an enduring impact on the future of healthcare. | 07/09/2025 |
| 954 | Applied Medical Rancho Santa Margarita, CA Process Engineer Bachelor’s degree in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-10 years |
As a Process Engineer, you will work within the Group Process Development team and use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. The Process Engineer’s primary responsibilities are debugging, observing, and expediting shop orders. You will assist with developing and updating engineering documents and investigating new tooling, materials, manufacturing processes, and technologies. | 07/09/2025 |
| 955 | Applied Medical Rancho Santa Margarita, CA Complaint Evaluation Engineer Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering or a similar engineering discipline Exp: 1 year |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. As a Complaint Evaluation Engineer, you will evaluate the performance of products returned by the customer. | 07/09/2025 |
| 956 | Applied Medical Lake Forest, CA Plastics Process Engineer Bachelor’s degree in Plastics, Manufacturing, Polymer, Materials, Mechanical Engineering, or a related engineering field Exp: 1 year |
Join Applied Medical and contribute to advancing the future of medical device manufacturing. As a Plastics Process Engineer, you will play a hands-on role in developing, optimizing, and supporting manufacturing processes with a strong focus on injection molding, heat treating, and complex part fabrication. This position offers a dynamic environment where engineers are deeply involved on the production floor, working closely with mold makers, process technicians, and production teams to make a direct impact on patient care. This is a project-management oriented role requiring strong coordination and follow-through. | 07/09/2025 |
| 957 | Applied Medical Cleveland, OH Materials Engineer Bachelor’s or Master’s degree in polymer science/engineering, chemistry, chemical engineering, materials science, or any other related fiel Exp: 0-2+ years |
As a Materials Engineer, you will be responsible for creating, monitoring, and controlling material related projects. You will provide materials expertise in projects that partner with design and manufacturing engineers and ensure manufacturability and performance of devices through proper material selection and processing. Additional projects will be in partnership with Quality Assurance in test method development and material characterization to help drive continuous improvement. The individual in this position will interface multiple R&D projects including design, preparation and execution of experiments, analysis and presentation of results, and coordination with external characterization laboratories. You will be expected to maintain and ensure a safe, organized, and efficient work environment. The materials tested in the laboratory will include a variety of thermoplastics, thermosets, coatings, adhesives, and silicone rubbers. | 07/09/2025 |
| 958 | Argonaut Manufacturing Services Carlsbad, CA Drug Product Manufacturing Associate I Bachelor's in an Engineering discipline or Life Science field Exp: 1-2 years |
The purpose of this position is to perform tasks and operations relevant to the bulk formulation and/or filling operations required for sterile production of liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing. | 07/09/2025 |
| 959 | Argonaut Manufacturing Services Carlsbad, CA Manufacturing Technician II Bachelor's degree in a related field Exp: 1 year |
The Manufacturing Associate II is responsible for executing all manufacturing department processes while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate II is expected to fully participate in both departmental projects and any quality working teams that may be applicable. This position shall be responsible for the hands-on execution of activities as they relate to the manufacturing of products. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. | 07/09/2025 |
| 960 | Argonaut Manufacturing Services Carlsbad, CA Visual Inspection Technician Bachelor's degree in an engineering discipline or life science field Exp: 0-2 years |
The purpose of this position is to participate in tasks related to the visual inspection of manufactured liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing as well as other types of visual inspection activities, as required. | 07/09/2025 |
| 961 | ARL Bio Pharma Oklahoma City, OK Chemist I - Analytical Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 07/09/2025 |
| 962 | ARL Bio Pharma Oklahoma City, OK Chemist I - Chemistry Bachelor’s degree in chemistry or related science Exp: 0-2 years |
This position assists in maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position provides a backup for the daily calibration and/or verification of the balances and pH meter when the Lab Technician is unavailable. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform tests commensurate with skill level with some supervision. | 07/09/2025 |
| 963 | ARL Bio Pharma Oklahoma City, OK Microbiologist I Bachelor’s degree in Microbiology or related science Exp: 0-2 years |
Under the supervision of the laboratory supervisor the Microbiologist I provides a high level of quality pharmaceutical microbiology testing as well as effective customer service to ARL Bio Pharma clients. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. | 07/09/2025 |
| 964 | VIATRIS St. Albans, VT Chemist SIII Bachelor's degree Exp: 0-2 years |
Every day, we rise to the challenge to make a difference and here’s how the Chemist role will make an impact: Key responsibilities for this role include: Performs and documents the analysis of samples following approved test methods. Calculate, check, and/or review data. Assist with method development, validation, and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 07/02/2025 |
| 965 | VIATRIS San Antonio, TX Associate Scientist QC Bachelor’s degree in Life Science Exp: 0-2 years |
Every day, we rise to the challenge to make a difference and here’s how the Associate Scientist, QC role will make an impact: Key responsibilities for this role include: Testing of chemical components or products. Will involve the use of major laboratory instruments and equipment: HPLC, GC, FTIR, UV/VIS, as well as utilizing wet chemicals skills. Analytical review of data to ensure calculations is complete and accurate. Performs quantitative chemical analyses of APIs and related materials under direct supervision following established procedures and guidelines using laboratory instrumentation such as gas chromatographs, liquid chromatographs, ultraviolet-visible spectrophotometers, etc. Performs microbiological analysis as required. Treats numerical data throughout chemical analysis by performing mathematical calculations such as determining concentrations (molarity, parts per million, normality, etc.) and statistical information (standard deviation, mean, etc.). Prepares necessary reagents and equipment to expedite the performance of analysis by measuring and/or weighing chemicals, missing, and standardizing solutions, and assembling equipment. Maintains accurate records by logging samples received, recording samples analyzed, procedures used, and results obtained on datasheets and/or laboratory notebook. Weights and calculates samples in the physical and chemical analysis of products using balances and measured volumetric containers. Recognizes and informs Group Leader about daily lab activity and analytical problems. Organizes and properly labels samples, sample preparations, volumetric solutions etc. Maintains area free of sample contamination restores equipment and supplies to designated area; participates in general housekeeping efforts. Must maintain compliance of assigned training plan. Participates in the company performance management program on a regular basis as per the established policy. Within area of responsibility, understand and comply with all DPT safety, environmental and quality practices and procedures as outlined in organizational/departmental guidelines and SOPs as well as applicable federal, state, and local regulations. Perform other duties as assigned. | 07/02/2025 |
| 966 | VIATRIS Morgantown, WV Chemist I Bachelor's degree Exp: 0-2 years |
Every day, we rise to the challenge to make a difference and here’s how the Chemist I role will make an impact: Key responsibilities for this role include: Perform pharmaceutical testing including, but not limited to, HPLC, GC, TLC, UV, dissolution and IR spectroscopy. Demonstrate ability to understand and perform testing in accordance with all pertinent SOPs and lab practices. Critically evaluate and audit data. Write technical analytical reports and procedures. Perform routine testing with a senior level mentor analyst. Perform other duties as assigned. | 07/02/2025 |
| 967 | Vivex Biologics Miami, FL Operations Processing Technician I Bachelor’s Degree in science or related Exp: 0-1 years |
The Operations Processing Technician I support the processing and documentation requirements of tissue during the cleaning, cutting, shaping, inspecting, and packaging operations for transplantation purposes. The Operations Processing Technician I is also responsible for ensuring that all equipment and supplies used for processing are maintained and ready for use, and that all Processing Room maintenance is completed daily while complying with Quality Assurance requirements as mandated by federal, state, and trade regulations. | 07/02/2025 |
| 968 | Waters Corporation Milford, MA Operations Quality Engineer I Bachelor’s degree in engineering, Mathematics, Business, Science Exp: 1-2 years |
Waters Corporation is currently seeking a Quality Engineer to join our organization. This individual is responsible for process quality, data analysis, and for the planning and execution of process improvement projects supporting the Milling department of the Machine Shop within the Milford plant. Responsibilities include leading investigations into product non-conformances, developing and reporting quality system metrics, supporting Statistical Process Control (SPC) initiatives, and driving projects related to product and process quality. This position is hands-on in a fast-paced environment which will interact with multiple functions (Process Engineering, R&D, and other operational departments) as well as additional supporting quality groups to resolve quality issues. | 07/02/2025 |
| 969 | West St. Petersburg, FL Tooling Process Improvement Engineer Bachelor's degree in engineering Exp: 1-3 years |
Support the design and implementation of progressive tooling dies, quality & manufacturing equipment. Contribute to upstream process improvements through use of Lean Six Sigma tools and identify root causes in product rejection. Works as part of a global team and provide technical support to various functional teams. | 07/02/2025 |
| 970 | West Kinston, NC Associate Process Engineer, Sterilization Bachelor’s or Master degree in Biology/ Microbiology /Chemistry or another scientific area Exp: 1-3+ years |
This role is key to developing and introducing process improvements, standards, life cycle management and validation in select process areas, helping to advance and transform West’s growing business, supporting capital investments and contributing to addressing complex assignments. This person has decision rights for his process area, and he/she will have the opportunity to drive the implementation of new innovative processes and technologies in cooperation with the engineering and quality assurance teams and the plants. | 07/02/2025 |
| 971 | HD Biosciences (Wuxi AppTec) San Diego, CA Research Associate II Bachelors in Biology related field Exp: 1-3 years |
Assisting and performing efficacy and PK-PD studies and developing new in vivo/ ex vivo assays and models with minimum supervision, as needed. Help to design, optimize and execute of pharmacology experiments for compound screening, compound mode of action and efficacy in mechanistic and disease models, e.g. syngeneic and xenograft tumor model, acute and chronic autoimmune/inflammatory conditions, and analyses and reporting of experiments or implantation, blood/tissue collection, etc. Assist with and perform other experiments as required. Working with the team to perform assay development, optimization, and validation projects. Following SOPs to perform compound receiving, registration, and management. Help to manage lab coordination | 07/02/2025 |
| 972 | WuXi Biologics Cranbury, NJ Bioprocessing Associate II, MFG DSP Bachelor's Degree or equivalent experience in Science, Engineering or related field Exp: 0-2 years |
Reporting to the Manufacturing Supervisor, Downstream, the Bioprocessing Associate I role will work with the wider Manufacturing teams to support the production of biological products at the MFG18 Cranbury facility. This role will be responsible for procedures and processes associated with the manufacture of Drug Substance. | 07/02/2025 |
| 973 | WuXi Biologics Cranbury, NJ Research Associate Co-op, Downstream Process Development BS or MS in Life Sciences or related field Exp: 0-2 years |
Designs, executes and authors downstream purification development, optimization, scale up and tech transfer. Collaborates with other internal PD teams during process development and tech transfer. Supports pilot production, GMP manufacturing and related investigation studies. | 07/02/2025 |
| 974 | WuXi Biologics Cranbury, NJ Research Associate Co-op, Cell Culture Process Development BS or MS in Life Sciences or related field Exp: 0-2 years |
Designs, executes and authors upstream cell culture development, optimization, scale up and tech transfer. Collaborates with other internal PD teams during process development and tech transfer. Partner with other internal PD teams during process tech transfer. | 07/02/2025 |
| 975 | WuXi Biologics Cranbury, NJ Associate Scientist, Quality Control Environmental Monitoring Bachelor's degree in Chemistry, Microbiology, Biochemistry or equivalent field Exp: 1+ years |
The QC EM Associate scientist/scientist is responsible for the quality and on-time collection of samples, EM (Environmental sampling), Water and Gas system sampling (when required) with raw material sampling to the various testing sections. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and GMP documentation. | 07/02/2025 |
| 976 | Xeris Biopharma Chicago, IL Scientist I, Analytical Development (Late Stage) M.S. in a nalytical chemistry Exp: 1-3 years |
This position is responsible for the development of analytical and characterization methods for a range of pharmaceutical dosage forms in support of formulation, process, and specification development. The Scientist I, Analytical Development will work with product development scientists (formulation and analytical) seeking to develop various therapeutic drug product formulations incorporating the company’s XeriSol and XeriJect technologies. This role will also support Quality Control and CMC with respect to establishing product specifications, stability programs, material qualification, method validation, method transfer and process validation. | 07/02/2025 |
| 977 | Yokogawa Newnan, GA Manufacturing Engineer BS degree in Engineering or Engineering Technology Exp: 1-5 years |
The function of the Local Manufacturing & Design Engineering group is to expand the Yokogawa product business by leading the implementation of new local products through local manufacturing (LM) and design while facilitating strong communication with our headquarters (YHQ), Product Management (PMG) and affiliates. There are four main product lines which the group supports: Analytical, Controllers/Recorders, Flow and Transmitters. This role is a combination of manufacturing and design engineering. You will be tasked with creation and maintenance of product drawings and BOM’s, developing procedures, maintaining product compliance and supporting the manufacturing lines. Reports to Local Manufacturing & Design Engineering Manager. | 07/02/2025 |
| 978 | 10x Genomics Pleasanton, CA Quality Engineer I Bachelor’s degree or Master’s degree in a scientific or engineering discipline Exp: 1 year |
We are seeking a Quality Engineer I to join our Quality team. This is an entry-level professional position where you will learn to apply professional concepts and company policies to resolve routine issues. As a Quality Engineer I, you will receive detailed instructions on all work and will have the opportunity to develop a foundational understanding of quality processes within the life sciences industry. You will collaborate with your team to solve problems and contribute to the completion of project milestones. Currently ISO 9001 certified, we are actively working towards ISO 13485 certification to further enhance our quality management systems. Individuals applying for this position must be self-starters, strategic thinkers, action driven, thrive in a fast-paced environment, excel at managing multiple priorities, succeed in communicating across the organization and with external partners, and provide immediate contribution. | 07/02/2025 |
| 979 | Abbott Altavista, VA Assistant Chemist - 2nd Shift Bachelor’s degree, science-related Exp: 1 year |
This position works out of our Altavista, VA location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. | 07/02/2025 |
| 980 | Abbott Temecula, CA Manufacturing Engineer Bachelors Degree Exp: 0-2 years |
Initiates and completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company. Prepares reports, publishes, and makes presentations to communicate findings. Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology. Understands engineering principles theories, concepts, practices and techniques. Develops knowledge in a field to become a recognized leader or authority in an area of specialization and applies this knowledge in leadership roles in the company. Incorporates business policies and procedures into task completion. Understands the business needs of the company, and has knowledge of the customer needs of our business. Understands the business cycle and foresight of emerging technologies trends. Cultivates internal and external network of resources to complete tasks. Serves has a resource in the selection orientation and training of new engineers and employees. May lead a project team, determining goals and objectives for the projects. Mentors employees by sharing technical expertise and providing feedback and guidance. Interacts cross functionally and with internal and external customers. Serves as a consultant for engineering or scientific interpretations and advice on significant matters. Acts as a spokesperson to customers on business unit current and future capabilities. Cultivates a wide range of internal networks and begins to develop an extensive external network of resources to facilitate completion of tasks. May lead a project team of moderate scope. Provides guidance to less experienced staff. Acts as a mentor to lower level individual contributors. Influence exerted at peer level and occasionally at first levels of management. Plans, organizes, and prioritizes own daily work routine to meet established schedule. Exercises authority and judgment within defined limits to determine appropriate action. Failure to achieve results or erroneous decisions or recommendations may cause delays in program schedules and may result in the allocation of additional resources. | 07/02/2025 |
| 981 | Abbott Columbus, OH Assistant Microbiologist - 3rd shift Science related Bachelor’s Degree Exp: 1 year |
Apply high quality scientific techniques in the microbiological analysis of raw ingredients, in-process production samples, finished product testing and environmental monitoring, to ensure that all products manufactured are fit for use. Be able to work with fellow microbiologist, with a high degree of motivation, attention to important details with clear communication to all team members. This is important due to the high degree of responsibility and working within a small group where each person is relied upon highly. Prioritize tasks to efficiently be completed with the most accurate results, and to communicate clearly and work together in a team environment. Product testing, Environmental testing, Raw ingredient testing. Documentation, Project work, Troubleshooting. Media preparation/general lab work | 07/02/2025 |
| 982 | Abbott Pleasanton, CA Systems Engineer I Bachelor’s Degree in Engineering (Biomedical, Mechanical, Computer, Electrical, or Software), Computer Science, or related discipline Exp: 6 months |
We are recruiting a Systems Engineer I to join our Abbott Heart Failure team in Pleasanton, CA, Burlington, MA or Atlanta, GA where we are focused on helping people with heart failure manage their health to ultimately change and save lives. The engineer will be primarily working on the CardioMEMS HF portfolio, which remotely monitors changes in pulmonary artery (PA) pressure, which is used to prevent worsening heart failure, lower heart failure mortality rates, and improve quality of life for our heart failure patients. Systems engineering defines, designs, tests, and integrates components, disciplines, and products within the CardioMEMS HF System, including implantable sensors, external reader systems used by clinicians and patients, mobile application software, and cloud-based web applications. The System Engineer will help execute tasks during design change projects and development of next generation products, including requirements definition and management, design documentation, and system testing, verification, and validation. | 07/02/2025 |
| 983 | Abbott St. Paul, MN Supplier Quality Engineer Bachelors degree in Engineering or Science Preferred Exp: 1-3 years |
Ability to effectively communicate, facilitate and organize project activities relating to ensuring supplier quality. Develops and manages project schedules to ensure deadlines are met. Serves as the primary Quality contact for suppliers and provides technical assistance to management for suppliers as requested. Works with supplier development engineering to performs on-site annual and critical component supplier audits to ensure compliance with Quality Systems procedures and CSI requirements. Generates audit reports and ensures supplier audit findings are tracked to timely and closure. Provides quality systems input to suppliers such as, but not limited to: statistical process control, gage R&R studies, and capability studies. Resolves supplier quality issues at incoming inspection and the production line. Provides project team leadership and conducts investigations relating to supplier quality issues. Completes non-conforming material reports (NCMR), supplier requests for change (SRC), supplier corrective action requests (SCARs) and monitors follow-up with assigned supplier base. Routinely reports on supplier performance per defined metrics to management and other team members. Represent Quality during audits and interface with FDA, ISO, or any external auditor. | 07/02/2025 |
| 984 | Abbott Temecula, CA Associate Quality Engineer Bachelor's or Master's degree Exp: 0-2+ years |
Our location in Temecula, CA, currently has an onsite opportunity for a Quality Engineer. Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. | 07/02/2025 |
| 985 | Abbott Casa Grande, AZ Analytical Chemist Science related Bachelor’s Degree Exp: 1 year |
This position is responsible for performing assays in accordance with required methods. Assure test results meet specification limits and that appropriate quality actions are taken to achieve acceptable product status. Enter data into a Laboratory Information Management System (LIMS) as well as any other applicable systems or documented on appropriate forms. Coordinate testing with processing stages and filing or drying requirements to ensure minimum downtime is occurred during processing, filling or drying operations. Set batch yields, optimizations and releasing product to the filling or dryer production departments from the Processing department. Conduct additional finished product testing including; line monitoring, dilution, carryover or any other required finished product testing. Assists with investigations of testing issues as required under any testing policies. Observe all safety rules and regulations. Reports incidents, near misses, and chemical spills in the proper manner to chemist acting as shift lead, front line leader, or manager. Wears all required personal protective equipment, participates in the Environmental Health and Safety Programs, and forwards any opportunities for improvement. | 07/02/2025 |
| 986 | AbbVie Worcester, MA Technician, Manufacturing II BS in Engineering Exp: 0+ years |
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process. | 07/02/2025 |
| 987 | AbbVie North Chicago, IL Associate Scientist II, Toxicology Study Coordinator Bachelor’s or Master's Degree Exp: 0-2 years |
The position of Associate Scientist, Toxicology Study Coordinator is in the Preclinical Safety group and will report to a manager in Toxicology. The Associate Toxicologist aides in the planning, conduct and reporting of non-GLP and GLP toxicology studies, acting to support the Study Director and regulatory infrastructure. | 07/02/2025 |
| 988 | AbbVie North Chicago, IL Associate Scientist, Chemistry II Master’s Degree Exp: 0-2 years |
The Process Chemistry group is responsible for inventing and executing the chemical processes and preparing active pharmaceutical ingredients (API) to enable toxicology studies, clinical trials, and drug product development for AbbVie’s pre-clinical and clinical candidates. We create valuable intellectual property through composition of matter, chemical processes, and technology, resulting in the development of safe and cost-effective commercial manufacturing processes. AbbVie Process Chemistry is seeking a highly motivated Automation Engineering Scientist I to conduct chemical process research and development, supporting projects from pre-clinical stages through commercialization. | 07/02/2025 |
| 989 | AbbVie Worcester, MA Associate Scientist, Process Development II Master’s Degree Exp: No exp |
The Bioprocess Development at the AbbVie Bioresearch Center in Worcester, MA is seeking a highly motivated junior Scientist to join the CHO Cell Line Development team. The Scientist will advance AbbVie’s biotherapeutics pipeline through the development and characterization of highly productive CHO cell lines suitable for cGMP protein manufacturing. The selected candidate will have good experience in mammalian cell culture and demonstrate good aseptic technique history, following standard protocol to generate and analyze precise, reliable, and reproducible data in a timely manner. The candidate will also need to demonstrate good communication, presentation, and technical writing skills, team-working spirit, and strong scientific thinking approach in problem solving. The position is based in AbbVie Bioresearch Centre, Worcester, MA. | 07/02/2025 |
| 990 | Abeona Therapeutics Cleveland, OH Inventory Logistics Associate Bachelor’s degree Exp: 1-4 years |
The Inventory Logistics Associate (ILA) assists in serving multiple business units within the Supply Chain Department. ILA’s will serve as the main conduit for shipping and receiving activities at Abeona Therapeutics location in Cleveland, OH. ILA’s will also support the organization and management of inventory ensuring all materials used in the manufacturing suites are processed and released from the Quality Departments. ILA’s will also be paramount in all aspects of Transportation of Drug Products to the qualified treatment centers for the associated Drug Product. | 07/02/2025 |
| 991 | Abeona Therapeutics Cleveland, OH Environmental Monitoring Associate BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 1-3 years |
The Quality Control Analyst I performs routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Performs Environmental Monitoring (EM) and associated activities. Interacts with employees internal and external to Quality Control. | 07/02/2025 |
| 992 | Abeona Therapeutics Cleveland, OH Quality Assurance Specialist, Supplier Quality Bachelor’s degree in related field Exp: 1 year |
The Specialist I, Supplier Quality will perform routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the release of materials in support of cGMP Operations. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above. | 07/02/2025 |
| 993 | Abeona Therapeutics Cleveland, OH Specialist I, Quality Assurance - Quality Operations Bachelor’s degree in related field Exp: 1 year |
The Specialist I, Quality Assurance performs routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the maintenance of the quality systems in support of a cGMP Operation for production processes relating to batch record review and release from start to end of manufacturing activities, in-process sampling / testing, primary and secondary packaging, label control, and document management ensuring procedural and regulatory compliance throughout the manufacturing process. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above and will support manufacturing and quality control as the production area Quality Assurance representative. | 07/02/2025 |
| 994 | AstraZeneca Waltham, MA Scientist, Bioscience BS in Biology, Biotechnology or other relevant area Exp: 1-2 years |
The GCB team is critical for delivering these cellular models and developing methods to prepare primary cell lines for projects aligned with our strategic objective of increasing the translatability of the cell models used in research. We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role of Scientist, GCB. | 07/02/2025 |
| 995 | Adare Pharma Solutions Vandalia, OH Chemist I - Day Shift Bachelor’s degree in Chemistry or closely related field Exp: 0-2 years |
The QC Chemist performs moderately complex physical and chemical testing of intermediate and finished products according to written procedures and trains less experienced Chemists as required. Also responsible for testing of cleaning samples for more complex systems and more advanced instrument maintenance. Responsible for timely analytical data reporting based on project timelines. | 07/02/2025 |
| 996 | ADMA Biologics Boca Raton, FL Chemist I Bioanalytics B.S. in Chemistry, Biochemistry, Molecular Biology, or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company dedicated to developing superior products for immunodeficient patients at risk of infection. Our commitment to this underserved population drives our innovation and hands-on approach to production and development, setting us apart in the industry. If you're seeking a dynamic, innovative, and growing company in the biopharmaceutical sector that values excellence and integrity, consider joining ADMA Biologics. We currently have an exciting opportunity for a Chemist I Bioanalytics in Boca Raton, FL! This position is responsible for performing quality control testing of raw materials, in-process, and final products, following general instructions on routine work and detailed instructions on new assignments. | 07/02/2025 |
| 997 | ADMA Biologics Boca Raton, FL Laboratory Technician - Automation Bachelor’s degree in related science discipline Exp: 0-2 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We have an exciting opportunity available for a Laboratory Technician - Automation in Boca Raton, FL! The Laboratory Technician - Automation performs automated laboratory testing to support hyperimmune products for ADMA Biologics. This position is responsible for the receipt, testing and on-time delivery of donor testing and maintaining a cGMP compliant laboratory. Maintaining communication with group leader or department manager to support cross-function relationships with plasma centers and ADMA plasma operations. | 07/02/2025 |
| 998 | ADMA Biologics Boca Raton, FL Specialist QA I - Manufacturing Oversight - Night Bachelor's Degree Exp: 1-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a QA Specialist I - Manufacturing Oversight - Night in Boca Raton, FL! The QA Specialist I - Manufacturing Oversight - Night performs manufacturing oversight activities to ensure compliance with policies and procedures. Oversight activities include, but are not limited to, real-time manufacturing batch record review, review of manufacturing documentation (logs, charts, etc.), and resolution of issues on the manufacturing floor. | 07/02/2025 |
| 999 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I BS/BA Exp: 0-2 years |
Manufacturing Associates work in either Upstream or Downstream teams and execute batch records, run, and monitor equipment, monitor production processes, and complete documentation in line with cGMP (current good manufacturing practices) and GDP (good documentation procedures). In their daily tasks, Manufacturing Associates always observe and follow safety procedures and Standard Operating Procedures (SOPs). Additionally, Manufacturing Associates work cross-functionally with QA, MSAT, Facilities, and other key departments to ensure ongoing manufacturing operations are successful, reliable, safe, and compliant. An Associate I assists with basic bioprocess operations in Manufacturing under supervision in compliance with established processes and standards. | 07/02/2025 |
| 1000 | AGC Biologics Bothell, WA Upstream Manufacturing Associate I BS/BA Exp: 0-2 years |
Manufacturing Associates work in either Upstream or Downstream teams and execute batch records, run, and monitor equipment, monitor production processes, and complete documentation in line with cGMP (current good manufacturing practices) and GDP (good documentation procedures). In their daily tasks, Manufacturing Associates always observe and follow safety procedures and Standard Operating Procedures (SOPs). Additionally, Manufacturing Associates work cross-functionally with QA, MSAT, Facilities, and other key departments to ensure ongoing manufacturing operations are successful, reliable, safe, and compliant. An Associate I assists with basic bioprocess operations in Manufacturing under supervision in compliance with established processes and standards. An Associate I assists with basic bioprocess operations in Manufacturing under supervision in compliance with established processes and standards. | 07/02/2025 |
| 1001 | Agilent Cedar Creek, TX Quality Associate Bachelor’s degree Exp: 1+ years |
Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Agilent is currently hiring a Quality Associate for our Cedar Creek site. | 07/02/2025 |
| 1002 | Agilent Wilmington, DE Electrical Engineer – Manufacturing Bachelor’s or Master’s degree in Electrical Engineering or a related technical discipline Exp: 1+ years |
At Agilent, we deliver trusted answers that advance the world of life sciences. As a Systems Engineer – Manufacturing, you will play a key role in ensuring our electrical systems and manufacturing processes meet the highest standards of quality, safety, and performance. This role is ideal for an engineer eager to collaborate across teams, solve complex problems, and contribute to continuous improvement in a fast-paced production environment. | 07/02/2025 |
| 1003 | Agilent Frederick, CO QC Analyst - 2nd Shift Bachelor’s or master’s Degree Exp: 1+ years |
As a QC Analyst, you will be responsible for conducting routine and non-routine analysis of raw materials, in-process items, and finished formulations according to standard operating procedures. Your role includes performing biochemical and chemical analyses to ensure product stability, compiling data for documentation, calibrating and maintaining lab equipment, and participating in investigations and report preparation. You may also develop testing methods, review data for compliance, revise standard operating procedures, and perform special projects related to analytical and instrument problem-solving. | 07/02/2025 |
| 1004 | Tempus Research Triangle Park, NC Molecular Technologist I-IV BS/BA or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Responsibilities: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 06/23/2025 |
| 1005 | Tessera Somerville, MA Research Associate II, Foundry MS in Biology, Chemistry, Biochemistry, Biotechnology or related field Exp: 0-2 years |
You are driven, motivated, and passionate about working at the forefront of RNA technology- contributing to groundbreaking research. You excel in both independent and team environments, possess impeccable attention to detail, and thrive in a fast-paced setting. Candidates without automation experience are still encouraged to apply. Tessera employees are creative and collaborative problem solvers. They have a strong sense of integrity and unwavering commitment to scientific excellence. | 06/23/2025 |
| 1006 | Tessera Somerville, MA Research Associate II/Senior Research Associate, Oligonucleotide Foundry MS in chemistry, biology, or related life sciences Exp: 1+ years |
You are a skilled individual who can operate in a fast-paced environment, troubleshoot instruments, and document operations independently and as part of a team. You will have the opportunity to organize and present results within the group and interface with other teams, so strong communication skills are critical. You enjoy overcoming challenges in collaboration with colleagues. Tessera employees are creative and collaborative problem solvers. They have a strong sense of integrity and unwavering commitment to scientific excellence. | 06/23/2025 |
| 1007 | Thermo Fisher Scientific Greenville, NC Sr Formulation Technician: Control Room & Lyophilizer Bachelor’s Exp: No exp |
The Sr. Formulation Technician will be able to perform tasks with little to no direction. They will provide guidance in the absence of the Lead Formulation Technician. They will be proficient in aseptic filling and manufacturing. This colleague follows written and verbal instructions using cGMP documents and operating equipment when performing the following duties. Shift hours are 6am-6pm on a 2-2-3 rotating schedule. | 06/23/2025 |
| 1008 | Thermo Fisher Scientific Richmond, VA Assistant Scientist Bachelor's degree Exp: 0-1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 06/23/2025 |
| 1009 | Thermo Fisher Scientific Plainville, MA Sr. Formulation Technician NTO Bachelor's Degree in a related field Exp: 1+ years |
Join our team at Thermo Fisher Scientific as an outstanding Sr. Formulation Technician and be a part of a world-class manufacturing environment. You will play a key role in producing detailed drug product injectables by operating advanced equipment and ensuring the highest quality standards. Your technical expertise will drive process optimizations and successful implementations, making a significant impact on our operations. This is a remarkable opportunity to showcase your skills in a collaborative and inclusive atmosphere! | 06/23/2025 |
| 1010 | Thermo Fisher Scientific Chicago, IL Scientist - HPLC, GMP Masters degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Exp: 0-2 years |
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. | 06/23/2025 |
| 1011 | Thermo Fisher Scientific Richmond, VA Assistant Scientist - 2nd Shift Bachelor's degree Exp: 0-1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 06/23/2025 |
| 1012 | Thermo Fisher Scientific Grand Island, NY QC Technician II Bachelors’ degree in Science related studies Exp: 1-2 years |
Incoming Quality Control Technician II performs wet chemical analyses and inspections on production commodities and raw materials (i.e. salts, sugars, amino acids, vitamins, etc) following established methods and SOPs in accordance to cGMPs. We need a motivated individual with excellent communication and laboratory skills to coordinate and complete planned and detailed activities within a quality system to ensure product, process, system, or equipment quality requirements are met. | 06/23/2025 |
| 1013 | Thermo Fisher Scientific Wilmington, DE Associate Scientist, Formulations Bachelor's degree in Biological Sciences, or other related degree concentration Exp: 1-2 years |
The associate scientist will perform a variety of routine to complex lab activities related to formulation and overall drug product development of large molecule drug products. The role involves designing and executing the experiments, document experimental details, organize the data, and summarize the findings in a technical summary report. The position emphasizes scientific rigor, collaboration with different functions, and effective communication of findings within the organization. | 06/23/2025 |
| 1014 | Transpire Bio Weston, FL Associate Formulation Scientist MS degree in Chemistry, Chemical/Biochemical Engineering, Biochemistry or a related scientific discipline Exp: 1-3 years |
In this role, the Associate Scientist I/II will provide hands-on formulation and process expertise during the development of clinical and commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts laboratory activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. | 06/23/2025 |
| 1015 | Transpire Bio Weston, FL Associate Scientist I BSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct laboratory activities with limited supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all testing performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of inhalation drug product. Prepare samples for blend uniformity. Perform equipment qualification and calibrations as directed. Execute approved method transfer protocols. Assist in the training of other scientists. Perform other tasks as assigned. Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicates effectively with team members. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate safety rules and procedures. Comply with all Corporate guidelines and policies | 06/23/2025 |
| 1016 | Transpire Bio Weston, FL Associate Scientist II MSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct laboratory activities with limited supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all testing performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of inhalation drug product. Prepare samples for blend uniformity. Perform equipment qualification and calibrations as directed. Execute approved method transfer protocols. Assist in the training of other scientists. Perform other tasks as assigned. Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicates effectively with team members. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate safety rules and procedures. Comply with all Corporate guidelines and policies | 06/23/2025 |
| 1017 | Transpire Bio Weston, FL Pharmaceutical Manufacturing Process Associate Scientist BS or MS Degree in Chemical/Biochemical Engineering, Chemistry, Biochemistry or a related scientific discipline Exp: BS 1-5 years; MS 0-3 years |
In this role, the Process Associate Scientist I/II will involve developing and optimizing pharmaceutical manufacturing processes, ensuring product quality and consistency, and complying with regulatory requirements on commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts pilot scale manufacturing activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. | 06/23/2025 |
| 1018 | Twist Bioscience South SF, CA Manufacturing Associate I, NGS Probe Production Bachelors degree in biology, chemistry, biochemistry Exp: 0-1 years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate, NGS TE will perform basic molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture of variety of custom oligonucleotide products. The ideal candidate will be able to work independently, be very neat and organized, have the ability to follow established SOPs and complete manufacturing batch records to contribute to the daily production schedule. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. They will uphold standards as defined by the manufacturing process, work on continuous improvement and have good time management resulting in efficiency, and work in a safe manner. | 06/23/2025 |
| 1019 | Twist Bioscience Portland, OR Automation Service Engineer BS in Engineering (Mechanical, Electrical/Electronics) or Biological Science field or related technical discipline Exp: 1-2 years |
The Engineering group at Twist is a team of diverse backgrounds (engineers, biologists and chemists) who have a huge and direct impact on Twist products. Our team designs and develops several new engineering solutions that are used in development and production and are critical to synthesis of oligos and DNA. As an Automation Service Engineer, you will own the support of scalable and robust solutions for custom oligo and gene products. These solutions will be an interesting combination of hardware, software and biological systems. The focus will be on liquid handling, mechanical design and data analytics. | 06/23/2025 |
| 1020 | Ultima Genomics Fremont, CA Product Engineer I BS or MS in Engineering or core scientific degree Exp: 1+ years |
We are looking for a highly motivated Product Engineer I to join our team! Our Product Engineer plays a strategically important role in ensuring the company’s business success. The primary responsibilities include, but are not limited to, supporting Field Service Engineers (FSEs) and Field Application Scientists (FASs) groups with technical support, authoring and reviewing Best Known Practices (BKPs) for field deployment, and coordinating the rollout and implementation of Engineering Change Orders (ECOs) in the field. In this Product Engineer (PE) position, you will train FSE’s on best practices and be the point of contact for field escalations. PEs are system experts and sometimes work side by side with R&D to gain a deep understanding of the system. PEs will help define problem statements, develop mitigations, and are a key contributor to Corrective Action Preventative Action (CAPA) plans. | 06/23/2025 |
| 1021 | United Therapeutics Manchester, NH Research Associate II - Tissue Engineering Master’s degree in a Biotechnology, Biomedical Engineering, or Cellular Biology field Exp: 1 year |
Execute laboratory cellular research tasks related to organ scaffold 3D printing; support the company’s goal of establishing new experimental procedures and analytical metrics to characterize the biological outcomes of different lung cell types on 3D printed lung scaffolds. Perform cell studies experiments to address the technical challenges with efficient post-processing of 3D printed objects. Implement biochemical assays to evaluate cell phenotypes after cellularization of 3D printed scaffolds, including imaging (bright field, confocal, lightsheet), immunostaining, and qPCR. Implement and evaluate culture methods using bioreactor systems. Perform biochemical assays following manufacturer instructions. Record and manage the use of the materials and reagents needed to carry out experiments. Record all laboratory data in the in-house data management systems. Prepare reports, technical documents and Standard Operating Procedures for internal and external use. Apply effective communication and data organization skills to report and present scientific data to other team members individually and at group meetings. Apply knowledge biological/biomedical/biotechnology concepts, standards and methods to execute 3D printing, scaffold processing, and bioreactor assembly for cellularization experiments. | 06/23/2025 |
| 1022 | United Therapeutics Research Triangle Park, NC Bioprocess Technician - Tissue Engineering Development Bachelor’s Degree in life science, engineering, or biomedical science Exp: 1+ years |
If you're passionate about advancing research for the treatment of pulmonary hypertension and other lung diseases, this role is for you! As part of our innovative research team, you’ll play a pivotal role in developing regenerative medicine products by operating lung recellularization systems and supporting tissue engineering processes. You’ll assist in preparing human and non-human tissues, performing assays, maintaining bioreactors, and analyzing data—contributing directly to the development of groundbreaking treatments. If you thrive in a collaborative, hands-on lab environment and are eager to apply your technical skills to real-world medical solutions, this position offers a unique opportunity to make a meaningful impact. | 06/23/2025 |
| 1023 | United Therapeutics Manchester, NH Associate Print Process Engineer Bachelor's degree in mechanical, chemical or biomedical engineering, or related field Exp: 1+ years |
We are looking for our “jack of all trades” to work on the worlds most advanced 3d printing technology printing the worlds most advanced 3d printed object ever – a human lung. If you want to take your SLA/DLP 3D printing experience to the next level and learn under a team of experience print engineers who love to teach and mentor, apply below. The Associate Print Process Engineer is responsible for systems development projects to build cutting edge 3D printers for lung scaffold printing. This work will support the development of methods to produce 3D printed lung scaffolds that are suitable for cellularization and will include both in-house development and coordinating with external partners to meet project milestones. | 06/23/2025 |
| 1024 | United Therapeutics Eden Prairie, MN Preclinical Research Associate I Bachelor’s Degree in biology, biomedical, or other related health fields Exp: 1+ years |
We are looking for our motivated, self starting human with a service mentality. This person will have experience with animals in a research setting and have an eye for details and data while being eager to learn all they can and make an impact. This is a once on a lifetime opportunity to take your preclinical experience and apply it to a product like transplantable kidneys or livers. Sound like something you want to be apart of? Apply below. The Preclinical Research Team works with small and large, cross-functional teams on our early and late-stage development projects to advance Miromatrix programs. The Preclinical Research Associate I will work with the Preclinical Team to support the planning and conducting of pre-clinical experiments, analyzing data, and documenting results that enable teams to make decisions and progress the programs towards the clinic. This position will attend procedures at regional contract research organization and universities to assist with data collection and study duties that support the goals of the preclinical program. | 06/23/2025 |
| 1025 | United Therapeutics Manchester, NH Print Process Engineer Masters Degree in mechanical, chemical or biomedical engineering, or related field Exp: 1 year |
We are looking for our “jack of all trades” to work on the worlds most advanced 3d printing technology printing the worlds most advanced 3d printed object ever – a human lung. This position is multi faceted and works at the center of different groups, technologies and hardware. Interested? Apply below! The Print Process Engineer is responsible for systems development projects to build cutting edge 3D printers for lung scaffold printing. This work will support the development of methods to produce 3D printed lung scaffolds that are suitable for cellularization and will include both in-house development and coordinating with external partners to meet project milestones. | 06/23/2025 |
| 1026 | Unither Manufacturing Rochester, NY QC Chemist Associate B.S. in chemistry or related science discipline Exp: 0+ years |
Performs routine analyses of materials, drug substances and drug products following cGMPs. May support analytical method development & validation, and analytical troubleshooting under technical supervision. Assists with maintaining lab quality systems. | 06/23/2025 |
| 1027 | Unither Manufacturing Rochester, NY Validation Technician BS Exp: No exp |
Assists validation efforts in many ways including the following: executes/supports equipment, cleaning, and process qualifications, takes and delivers samples, collects and compiles data for validation reports, assists in maintaining of the Validation Document Library, maintains test equipment and documentation system. | 06/23/2025 |
| 1028 | Valo Health New York, NY Engineer I, Tissue Engineering Bachelor’s degree in mechanical, electrical or biomedical engineering Exp: 1+ years |
As a Tissue Engineer I within the Translational Biology department, you will be part of a team of data scientists, translational biologists, and engineers building a powerful computational platform for advancing the research and development of new medicines. You will work on the BiowireTM platform, which generates biofidelic engineered human cardiac and skeletal muscle tissues. BiowireTM is a cornerstone of the larger Opal Computational PlatformTM which evaluates the safety and efficacy of drugs in various models at a decreased cost as compared to human trials, and ethically as compared to animal testing. Successful candidates will work with a diverse set of scientists and engineers in ways that cut across traditional industry boundaries. | 06/23/2025 |
| 1029 | Vantage MedTech Lenexa, KS NPI Engineer BS or MS degree in Engineering, preferably Mechanical or Manufacturing Engineering. Exp: 1-3 years |
The NPI (New Product Introduction) Engineer will be responsible for ensuring that our innovative designs are transitioned into effective and sustainable production. Our life saving products are manufactured in Kansas City and require predictable delivery of high quality, cost-effective production over 5+ year product lifetimes. You will collaborate with Vantage MedTech’s Engineering and Manufacturing teams to provide input on the device design’s manufacturability, and plan and execute the transfer of these new products to our manufacturing facility. You will be responsible for ensuring that robust manufacturing processes are created, updated and in compliance with company standards, ISO, and GMP as required. In addition, you will help drive improvement projects that impact quality and productivity. | 06/23/2025 |
| 1030 | Vector Laboratories Newark, CA Manufacturing Associate I, NGS Probe Production BS or BA degree in Chemistry Exp: 0-3 years |
The Manufacturing Associate I is primarily responsible for manufacturing Vector’s products according to established procedures and documenting all work in production batch records using established good documentation practices. The Manufacturing Associate I will operate and maintain common laboratory equipment as per instructions and works under general supervision on assigned tasks. Technical expertise should include strong knowledge of general laboratory safety and practices, basic knowledge of modern synthetic organic chemistry, multistep synthesis, and purification technique. This position will report to the Site Leader. | 06/23/2025 |
| 1031 | Phillips Medisize Costa Mesa, CA Quality Engineer Bachelor's Degree in an Engineering Field Exp: 1+ years |
Use quality tools to implement improvements including: process flowcharting, Pareto analysis, correlation and regression analysis, significance tests, design of experiments, statistical process control, gauge repeatability and reproducibility, and trend analysis techniques. Assist the development of essential QMS deliverables/Advanced Product Quality Planning (APQP) including, but not limited to: complaint analysis, risk analysis, failure mode and effects analysis, CAPA, and process/equipment/software verification / validation. Monitor production processes and products for adherence to company and regulatory standards and practices. Participate in quality improvement initiatives and projects. Perform quality reviews and internal audits; evaluate data and write reports to validate or indicate deviations from existing standards. Review and approve change requests. Manage the qualification of processes performed by suppliers; troubleshoot and lead corrective actions relating to supplier performance; improve process for supplier data submission to reduce internal inspections. Facilitate communication between engineering, manufacturing, and quality functions. Responsible for being a communication liaison between the customer and manufacturing facility. | 06/23/2025 |
| 1032 | Phillips-Medisize Hudson, WI Validation Engineer Bachelor’s Degree in a scientific discipline Exp: 1+ years |
Coordinate and lead validation projects and discussions. Work with project teams to define the validation strategy. Draft MVPs, equipment qualification, protocol/test case, deviations and summary report documentation for project wrap up. Execute computer system/software validation activities including risk assessments and part 11 compliance requirements. Interface with customers to resolve issues and harmonize validation requirements. Learn and deploy SAP related tools and deliverables associated with validation documents and document approval workflows. Provide statistical analysis support to sites and validation teams. Assist with creating, updating, and training on WI, SOP, and other necessary documents needed to perform validation work. Support global rollout of Global Validation requirements and on-site or desk audits of Phillips-Medisize sites to ensure compliance to the global standards. Share validation best practices information and suggest improvement opportunities. Travel to other Wisconsin Phillips Medisize sites (up to 50%) with occasional travel outside Wisconsin as needed. | 06/23/2025 |
| 1033 | Velocity Clinical Research Durham, NC Clinical Research Coordinator I Bachelor’s degree Exp: 1 year |
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. | 06/23/2025 |
| 1034 | Veloxity Peoria, IL Associate Scientist II Bachelor’s degree in science (chemistry/biochemistry preferred) Exp: 1-2 years |
As an Associate Scientist II, you will be using state-of-the art technologies to perform bioanalytical testing for emerging pharmaceutical and biopharma companies. At Veloxity, we hire driven and motivated individuals and provide training and career advancement opportunities within our organization. | 06/23/2025 |
| 1035 | Veracyte Austin, TX Specimen Processor Bachelor’s degree Exp: 0-2 years |
The Specimen Processor in this CLIA Laboratory is a critical member of the laboratory team, responsible for receiving, accessioning, and documenting specimens with precision. This role requires accurate data entry, proactive identification, and resolution of sample integrity issues. Flexibility in scheduling, including holidays and variable shifts, is essential to meet operational demands. | 06/23/2025 |
| 1036 | Vertex Pharmaceuticals San Diego, CA Protein Sciences Senior Research Associate Masters Degree in biological sciences Exp: 0-2 years |
Vertex Pharmaceuticals is seeking a highly motivated Senior Research Associate to join the Protein Sciences team in San Diego. The Protein Sciences team is responsible for guiding our drug discovery programs through key molecular insights that underlie disease target function and modulation. The successful candidate will support the advancement of our research programs to create transformative medicines for patients with serious diseases through the generation of high-quality recombinant proteins for biochemical, biophysical and / or structural biology experiments. | 06/23/2025 |
| 1037 | Alora Pharmaceuticals Forth Worth, TX QC Chemist I BA/BS in Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 06/23/2025 |
| 1038 | Alora Pharmaceuticals Forth Worth, TX QC Chemist II BA/BS Chemistry Exp: 1 year |
A Chemist II completes testing independently. May perform non-routine method transfer and instrument troubleshooting with supervision if required. A Chemist II has good oral and written communication skills. A Chemist II has strong lab-work skills and good understanding of chemical testing equipment and processes. A Chemist II has a good understanding of cGMP, DEA regulations, and Quality Procedures for working in a QC Lab. A Chemist II knows the basic concepts of statistical treatment of experimental data. Proposes conclusion congruent with experimental results. A Chemist II can identify routine technical problems and seeks help to solve them. Knows basic skills for OOS, OOT, and aberrant result investigations. A Chemist II has proficient level of understanding of lab instruments and equipment knowledge and basic trouble shooting skills. | 06/23/2025 |
| 1039 | Alora Pharmaceuticals Marietta, GA Process & Product Development Scientist - Osmotica Bachelor's or Masters degree in chemistry, engineering, pharmacy or a related scientific discipline. Exp: 0-3 years |
The incumbent is responsible for supporting Technology Transfer and Product Development of pharmaceutical dosage forms and drug delivery systems for new and existing chemical entities according to approved plans/protocols. The Process and Development Scientist is responsible for developing, organizing, and leading development activities in the manufacturing area and performing developmental activities. The Process and Development Scientist also performs related technical writing functions, including Standard Operating Procedures (SOPs). The incumbent is also responsible for operating the laboratory process and testing related equipment in the Pharmaceutical Sciences Laboratory. | 06/23/2025 |
| 1040 | VGXI Conroe, The Woodlands, TX Environmental Monitoring Technician Bachelor’s degree Exp: 1-3 years |
The primary responsibility of Environmental Monitoring Technician is to perform all EM monitoring and related testing, water sampling and testing. Responsibilities also could include in-process and release testing of products manufactured at VGXI. Set-up, organization, and day-to-day operations of a Quality Control Lab are also required. | 06/23/2025 |
| 1041 | VGXI Conroe, The Woodlands, TX Upstream & Downstream Manufacturing Process Technicians Bachelor’s degree Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid-based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for upstream/downstream operations. Maintains records, process, and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Upstream/Downstream Manufacturing. Understands and applies biological, chemical, and mechanical principles and techniques. | 06/23/2025 |
| 1042 | PerkinElmer Annapolis, MD CCFS Media Prep Technician Bachelor Degree in a chemistry, biology, or other relevant discipline Exp: 0-1 years |
Work with Cell Culture and Fermentation Suite scientists to prepare cell culture media, feed, stocks, buffers and reagents. Primary duties will include preparing many types of biological cell culture basal media, nutrient feed and stock solutions for NS0, CHO and hybridoma cells. Solutions will be tested for osmolarity, pH, and turbidity. Using aseptic technique and a biological safety cabinet, filter or pump solution into sterile containers as requested by scientists and store all solutions properly. Lab instrument maintenance for Nova, Cedex, BGA, pH meter and osmometer as schedule permits. Monitor stock solution inventory and prepare as needed. Label all solutions according to CCFS guidelines. Work with scientists to prepare custom solutions and make modifications as needed to standard media and feed formulations. Update the Solution Preparation Console daily to reflect all lot numbers, catalog numbers and formulation modifications as well as storage conditions. Calibrate laboratory equipment as required. Clean and sterilize BSC according to schedule. Monitor inventory in cold room and feed cabinet, discarding expired solutions and maintaining stock of general use solutions. Maintain inventory of all chemicals in the cold room and media prep laboratory. Receive chemicals, barcode, and log into the Chemical Inventory Console. Retire chemicals from the inventory console as needed. Provide support with the design of small bioreactor performance of experiments on media stability. Assist in the preparation of laboratory SOPs. Maintain work environment to guarantee the success of aseptic operations. Record and keep accurate material inventory and update database. Keep laboratory notebooks up to date. Communicate effectively with internal customers. Maintain training and compliance in areas of health and safety, security, environmental and operational aspects of daily activities in the working environment. May require support of on-call service for specific research units in the lab areas. Hours are between 5:00pm-7:30am Monday thru Sunday. Tasks include but are not limited to transfer of contents from failing fridges and incubators to designated back up units, photograph original items, properly document failure, provide a work order of failing unit to facilities team and inform respective end-users about the transfer via email based on the SOP instructions. | 06/23/2025 |
| 1043 | Viant Laconia, NH Quality Engineer Bachelor’s Degree in Engineering or related field Exp: 0-2 years |
The primary purpose of this role is to support Operations by ensuring adherence to Quality System requirements for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance. | 06/23/2025 |
| 1044 | scPharmaceuticals Burlington, MA Quality Associate Bachelor’s Degree Exp: 1+ years |
The role of The Quality Associate will support the company’s quality and regulatory systems in compliance with industry best practices. They will primarily support the Product Complaint Handling process. This position reports to the Quality Director. | 06/18/2025 |
| 1045 | Pfizer McPherson, KS EHS Senior Associate Master's degree Exp: 0 years |
The successful candidate will be part of a dynamic team of experts who form Pfizer’s Environment, Health, & Safety division. Due to the importance of this team for Pfizer’s employees and patients, the organization relies heavily on its team members’ timely actions and efficiency. You will be responsible for activities involved in identifying hazardous workplace conditions and take effective steps to ensure that workplace conditions comply with applicable federal and state Occupational Safety and Health standard provisions. You will assist in the development and implementation of short- and long-range plans and continuously improve EHS performance. As a Senior Associate, your ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. | 06/18/2025 |
| 1046 | Pfizer Sanford, NC QC Scientist Method Transfer and Validation Master's degree Exp: 0+ years |
You should be able to review the validation data as a second analyst reviewer. Ensures that quality control procedures adequately evaluate an organization's products. Determines if current methods and techniques result in meeting reliability standards or require modification. (More concerned with standards, methods and procedures than with testing devices and equipment used to check products). Devises testing plans, methods and equipment to assure reliability of product in conjunction with product design and specifications. (More concerned with tests and quality control checks during and after product preparation.) Tests and inspects products to determine compliance with specifications. Include on- and off-line inspection. Performs laboratory tests on finished products, raw materials, and in-process material in support of the company's quality control program. Prepares reports and/or exercises administrative control in support of the company's quality control program. | 06/18/2025 |
| 1047 | Pfizer Sanford, NC QC Senior Associate Scientist - Method Transfer and Validation Master's degree Exp: 0+ years |
The resource will work on-site at the Pfizer, Sanford, North Carolina facility and will be a member of Pfizer’s Quality Control Portfolio Management team to support multiple quality programs. You will be able to perform chemical, or biological or microbiological analysis on products. The colleague should be able to perform the analytical or chemical or microbial and sterility testing in the GMP laboratory setting and should be able to collaborate efficiently with the external teams. Additionally, the candidate should be able to document all the data to in accordance with cGMP and data integrity principles. | 06/18/2025 |
| 1048 | Pfizer Rocky Mount, NC QC Lab Analyst II Bachelor’s degree Exp: 0+ years |
The QC Chemistry Lab Analyst IIwill perform basic analysis for raw materials, in process and finished products a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality. Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required. | 06/18/2025 |
| 1049 | Pfizer Rocky Mount, NC QC Chemistry Lab Analyst II Bachelor’s degree Exp: 0+ years |
The CQ Lab Analyst II, will perform basic analysis for Validation of new and existing products on manufacturing lines in a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of multiple sample sites across the manufacturing process to demonstrate that our process is able to meet the high standards of quality for patient use. Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required. | 06/18/2025 |
| 1050 | Pfizer Rocky Mount, NC QC Senior Scientist Master's degree Exp: 0+ years |
QC Senior Scientist will be recognized as a technical expert and a scientific contributor. With the deep knowledge of the discipline, QC Sr. Scientist will be an active team member whose decisions impact the project. QC Sr. Scientist will be using scientific judgment to adapt standard methods and techniques by applying prior work experience. QC Sr. Scientist will be forecasting and planning resource requirements for project team. QC Sr. Scientist creativity in developing novel processes and new ideas will be used frequently. QC Sr. Scientist will undertake mentoring activities to guide team members. | 06/18/2025 |
| 1051 | Pfizer Pearl River, NY Sr Associate Scientist - Conjugation MS degree in Chemistry/Organic Chemistry or related discipline Exp: 0-4 years |
As a Senior Associate Scientist in the Early Bioprocess Development within Pfizer Vaccine Research and Development, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will join a large team of Scientists focused on conjugation process development for manufacturing carbohydrate-based conjugate vaccines. Primary duties include supporting the development and optimization of conjugation methods, purification, and analysis of intermediates and glycoconjugates using chemical and chromatographic methods. The individual will become a key contributor towards supporting the early development and scale up of glycoconjugate vaccines. Careful documentation of work and presentation of data is required. All work is to be done in a compliant manner according to SOP guidelines and cGMP/GLP regulations, where applicable. | 06/18/2025 |
| 1052 | Sequel Med Tech Manchester, NH Postmarket Quality Engineer Bachelor's degree in a technical field Exp: 1+ years |
The Quality Engineer will be a key member of our growing Post Market Surveillance team as we build our Quality Management System. The Quality Engineer will primarily support post market surveillance processes, but may provide support across the QMS, including maintaining and improving Quality Management System processes, supporting corrective and preventive actions, quality engineering support for complaint investigations, and field actions, as needed. This is an office-based position in Manchester, NH. | 06/18/2025 |
| 1053 | Sequel Med Tech Manchester, NH Quality Engineer Bachelor's degree in a technical field Exp: 1+ years |
The Quality Engineer will be a key member of our growing Quality/Regulatory team as we build our Quality Management System. The Quality Engineer will provide support across the QMS which may include responsibility for maintaining and improving the Quality Management System processes, control of documents and training materials, and quality engineering support for product development, and supplier management. This is an office-based position in Manchester, NH. | 06/18/2025 |
| 1054 | Siegfried Irvine, CA Quality Assurance Associate II BS degree in Biochemistry, Chemistry, Engineering, Biology or closely related Exp: 1-2 years |
This position supports the Quality Assurance Operation, which consists of QA shop floor supports, and QA batch review and Product Release. | 06/18/2025 |
| 1055 | Boston Scientific Quincy, IL Quality Engineer I Bachelor's Degree in engineering related field Exp: 6+ months |
The Quality Engineer I will utilize quality-engineering methodologies, systems, and practices to directly support the inbound and outbound distribution of Boston Scientific Cardiac Rhythm Management (CRM) and Neuromodulation (NMD) products within the Quincy, MA distribution center. This engineer will play a key role in ensuring the day-to-day supply chain executes successfully – supplying medical devices real time to BSC customers around the world. | 06/18/2025 |
| 1056 | Singota Solutions Bloomington, IN Quality Associate 1 - Quality Events Bachelor’s Degree – Science related field Exp: 1-3 years |
The Quality Associate 1- Quality Events position is responsible for supporting and maintaining the GMP-compliant quality systems related to deviations and CAPAs (Corrective Action & Preventative Action). This role provides quality oversight of quality event lifecycle management, ensures adherence to internal procedures and regulatory requirements, and interfaces directly with internal teams, external clients, and regulatory bodies. This position plays a key role in maintaining site compliance and driving continuous improvement across operations. | 06/18/2025 |
| 1057 | Revvity Remote, NJ Field Service Engineer BS/BA in a STEM field Exp: 0-2+ years |
Revvity is seeking a qualified candidate to join the Service Team in our Life Sciences & Diagnostics Business Unit. The individual will be responsible for supporting several testing labs in the greater New York City and New Jersey area. | 06/18/2025 |
| 1058 | SMC, Ltd Concord, NC Quality Control Technician Bachelor’s degree in Microbiology, Chemistry, Biochemistry, or a related field Exp: 1-2 years |
The Quality Control (QC) Technician is an entry level position that supports daily operations of the Quality Control department within the pharmaceutical manufacturing environment. This role involves routine activities that contribute to maintaining product quality and compliance. The ideal candidate is detail-oriented, dependable, and comfortable working in a regulated setting. Flexibility with scheduling, including early or late shifts and occasional weekend work, is required. | 06/18/2025 |
| 1059 | Smithers Gaithersburg, MD Scientist MS in biology, life sciences, or chemistry field Exp: 1 year |
Smithers PDS is seeking a Scientist to join our team in Gaithersburg, MD. The Scientist performs data analysis and various assays according to SOP with reliability while applying and meeting GLP, GCP, and/or CLIA requirements. This position assists with ensuring that the lab, materials, and equipment are maintained. | 06/18/2025 |
| 1060 | Smithers Columbus, OH Associate Microbiologist B.S. degree in microbiology or related field Exp: 6 months |
The Associate Microbiologist will conduct microbiological analysis of cannabis flower, concentrates and infused products as required by the state cannabis regulatory body regulations within an ISO 17025 accredited laboratory. The Associate Microbiologist will be responsible for coordinating scheduling with the Laboratory Manager, conducting sample analysis, and entering sample information into the laboratory information management system (LIMS). As time allows, the Associate Microbiologist will also be cross-trained to conduct sample preparation and extraction for subsequent chemical analyses. | 06/18/2025 |
| 1061 | Sonothera South SF, CA Research Associate/Sr. Research Associate, Histology Bachelor’s degree in Biology, Neuroscience, or related field Exp: 0-3 years |
The Gene Therapy group at SonoThera is seeking to hire a Research Associate/Senior Research Associate to become an integral part of the gene therapy drug development effort. We seek candidates who think critically and have the desire and ability to learn new techniques. This position requires adaptability and an ability to perform at a high level in a fast-paced environment. A qualified candidate will have broad technical experience in sample processing for histology. | 06/18/2025 |
| 1062 | Standard BioTools Boulder, CO Research Associate I BS or MS in molecular biology, biochemistry, chemistry or related field Exp: 1-3 years |
As part of the Assay R&D team, RA I will contribute to both new product development at all phases and sustaining activities related to existing products. New product development activities will be primarily related to SomaScan products (e.g., new assay formats, expanded content, alternative readouts). Additional tasks related to other SBI product lines including KREX or microfluidic applications will also fall within the scope of the RAI’s role. They will be involved in troubleshooting activities related to assay or instrumentation failures and perform tasks related to maintaining existing product lines. A successful candidate will have strong laboratory bench skills, particularly when executing biochemical laboratory techniques. The ideal candidate will additionally have proven experience designing and executing complex experiments in an R&D environment. | 06/18/2025 |
| 1063 | Starkey Eden Prairie, MN Regulatory Affairs Specialist I BS or MS in Science or Engineering Exp: 1-2 years |
This position is responsible for supporting the Regulatory Affairs Department for all medical devices and hearing related products. This position will work with various departments across the organization with focus on new product development. The Regulatory Affairs Specialist is responsible for supporting activities that keeps Starkey current with changes to medical device regulation and for creating and maintaining the technical files for all medical devices and hearing related products. | 06/18/2025 |
| 1064 | STERIS Coon Rapids, MN Quality Analyst Bachelors degree (Scientific or related technical field) Exp: 1 year |
The Quality Analyst in the STERIS Applied Sterilization Technologies (AST) Coon Rapids, Minnesota facility is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. The Quality Analyst executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. | 06/18/2025 |
| 1065 | STERIS Montgomery, AL Quality Engineer Bachelor’s Degree in Engineering or related technical field Exp: 1 year |
The Quality Engineer in our Montgomery AL location is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. The Quality Engineer supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 06/18/2025 |
| 1066 | STERIS St. Louis, MO Quality Engineer BS Chemical, Biochemical or Biomolecular Chemical Engineering. Exp: 1 year |
The Quality Engineer in our St. Louis, Missouri facility is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. As a Quality Engineer, you will support complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 06/18/2025 |
| 1067 | STERIS Conoroe, TX Quality Engineer Bachelor’s Degree Engineering or related technical field Exp: 1+ years |
The Quality Engineer in our Conroe, Texas facility is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. As a Quality Engineer, you will support complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 06/18/2025 |
| 1068 | STERIS Mentor, OH Quality Analyst Bachelors degree (Scientific or related technical field) Exp: 1 year |
The Quality Analyst in our STERIS Applied Sterilization Technologies (AST) Mentor, OH facility is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. The Quality Analyst executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. | 06/18/2025 |
| 1069 | STERIS Liberetyville, IL Scientist I B.S. degree in a technical discipline Exp: 1-3 years |
This Scientist I is responsible for the activities related to validation of sterilization processes across STERIS operating facilities. Activities include calibration of data collection systems, such as maintaining dosimeters and dosimetry equipment, measurement of dosimeters for report generation; operation, and data collection related to portable temperature/humidity sensors; coordinating with external laboratories for equipment calibrations and maintenance; coordinating with Customers for test sample processing and requalification studies; coordination and proper handling of product samples for transfer to outside laboratories for testing; and other routine tasks as directed by the immediate supervisor or manager. | 06/18/2025 |
| 1070 | Sterling Germantown, WI Analytical Chemist Bachelors Degree in Chemistry or related field Exp: 0-2 years |
As the Analytical Chemist at Sterling, you will be accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. Testing performed directly supports manufacturing through the release of raw materials, intermediates and API’s; as well as in-process controls, equipment cleaning verification, reference standard qualification, and stability program. The Analytical Chemist will develop the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data working. | 06/18/2025 |
| 1071 | Strand Therapeutics Boston, MA Associate Scientist, Analytical Operations M.S. in Chemical Engineering, Bioengineering or similar Exp: 1-2 years |
Strand is looking for people who have the enthusiasm and motivation to be a highly contributing member of a small but extremely productive team. This opportunity will offer the employee the ability to work in a matrix-based environment and be a part of the future strategy of the company. We are looking for a highly motivated and innovative candidate for the role of Associate Scientist of Analytical Operations. This individual will support in day-to-day analytical operations as an analyst. Reporting initially to the Senior Scientist of Analytical Development, the right candidate will be a strategic thinker that brings a leadership presence and enthusiasm for Strand along with a deep scientific knowledge. | 06/18/2025 |
| 1072 | Stryker Portage, MI Electrical Engineer, R&D Sustainment Bachelor's degree in Electrical Engineering Exp: 0+ years |
This Electrical Engineer role will support sustainment projects, working with other product engineers, R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to ensure project success. With coaching and mentorship, you will develop, modify, evaluate, and verify electronic components for medical devices. This is a unique opportunity to learn all areas of Stryker and to work with a variety of products. The project timeline is fast paced, and you will work to both solve problems and create efficiencies within the Stryker Instruments product lines. | 06/18/2025 |
| 1073 | Stryker Fort Lauderdale, FL Systems Engineer - DRE Bachelor of Science in Robotics, Electrical, Mechanical, Systems, or Biomedical Engineering Exp: 0+ years |
We’ve created new grad engineering roles within our DRE (Digital, Robotics and Enabling Technologies) organization in Weston, FL to invest in the next generation of innovators—accelerating their growth as engineers while building the future of Stryker. | 06/18/2025 |
| 1074 | Supernus Pharmaceuticals Rockville, MD Quality Control Chemist BS degree in Chemistry or other science-related discipline Exp: 1+ years |
Responsible for performing testing pharmaceutical solid dosage forms for release and stability, primarily by dissolution, and HPLC; maintaining proper GMP documentation for logbooks and report writing as necessary. | 06/18/2025 |
| 1075 | SystImmune Redmond, WA Research Associate/Senior Research Associate BS or MS in immunology, biochemistry, molecular biology, structural biology, or a related field Exp: 1+ years |
We are seeking a skilled Research Associate/Senior Research Associate with experience in utilizing display technologies (yeast/phage) in protein engineering, directed evolution, or binder discovery. This is a laboratory-based role that will be supporting protein engineering efforts in discovering novel binders and novel protein leads/scaffolds. The position will join a growing protein engineering team in an innovative organization and reports to the Director of Protein Engineering. The ideal candidate will be a quick learner with a broad experience set with direct expertise in a display technology and/or an adjacent field including but not limited to high throughput molecular biology, antibody/binder discovery, and protein engineering. Industry experience in biologics drug development is required. | 06/18/2025 |
| 1076 | SystImmune Redmond, WA Research Associate/Senior Research Associate - Cell Science Bachelor’s degree in biology or a related science major Exp: 1+ years |
Located in Redmond WA, Systimmune Inc.is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic multi-specific antibodies, as well as antibody-drug conjugates (ADCs). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. We are seeking a Research Associate / Senior Research Associate with experience in cell culture and plasmid preparation to join our Cell Science Department. | 06/18/2025 |
| 1077 | TAE Life Sciences Santa Monica, CA Research Associate, Molecular Biology BS/MS in Molecular Biology, Cell Biology, Biochemistry or equivalent Exp: 1-3 years |
We are seeking a highly talented and motivated individual with a strong background in molecular/cell biology to join our Molecular Biology group in the pursuit of developing novel therapeutic agents. The successful candidate will be responsible for generating and evaluating product candidates, with focus on performing experiments using recombinant DNA technology and developing antibody library construction and screening platforms. This role works in a collaboration with Protein Science, Translational Research, and Chemistry/Bioconjugation groups, onsite in a lab environment. | 06/18/2025 |
| 1078 | Takeda Boston, MA Research Associate, Analytical Development Bachelor’s degree in biology, biomedical engineering, or related pharmaceutical science Exp: 1+ years |
The Research Associate will play an integral part in sample testing, data analysis, workflow streamlining, automation, and method technology transfers. The Research Associate will be highly motivated, a team player mindset, great attention to detail, a high emotional IQ, and a foundation in science. This role will contribute to developing and executing analytical methods crucial for ensuring the quality, safety, and efficacy of cell-based therapeutics. | 06/18/2025 |
| 1079 | Takeda Boston, MA Research Senior Associate, Cell Therapy Master’s degree in Biotechnology, Immunology, Molecular Biology, Biomedical Engineering or related scientific field or related field Exp: 1 year |
Takeda Development Center Americas, Inc. is seeking a Research Senior Associate, Cell Therapy with the following duties: Plan and independently execute in vitro experiments to deliver data for cell therapy discovery platforms; Scope of experiments include production of engineered human and mouse T cells, proof-of-concept studies, target identification and selection, lead optimization, and functional assessments; Adapt or develop, evaluate, and troubleshoot in vitro and ex vivo experimental techniques; Create, compile, analyze, and record experimental data; Review, interpret, and present results internally in research team and cross-departmental meetings; Serve as a technical resource in the laboratory for other employees by demonstrating techniques and preparing study protocols and internal technical transfer documentation; Utilize scientific literature to increase knowledge base and implement improvements; Assist with development of project strategy; up to 20% remote work allowed. | 06/18/2025 |
| 1080 | Takeda Boston, MA Research Senior Associate, Oncology Cell Therapy Master’s degree in Biotechnology or related field Exp: 1 year |
Takeda Development Center Americas, Inc. is seeking a Research Senior Associate, Oncology Cell Therapy with the following duties: maintain primary immune cell cultures and produce human and mouse CAR T cells. Plan, prioritize, and execute CAR gamma-delta T cell production, applying leadership qualities to facilitate a seamless workflow for experiments. Establish new experimental designs for CAR T cells co-cultured with differentially activated fibroblasts and other target cell types using a range of techniques and analytical method such as ELISA/MSD, flow cytometry, cytotoxicity readouts, and/or gene expression. Produce, titer, and bank viral vectors to express CAR and other constructs in T cells. Collaborate with project representatives to plan experiments, analyze and interpret data, and communicate findings internally. Prepare study protocols, reports, and documentation. Work with manager and teammates to troubleshoot complex problems in creative and effective ways. Actively participate in the innovation and optimization of cell therapy processes to ensure the delivery of project goals. Up to 20% remote work allowed. | 06/18/2025 |
| 1081 | Takeda Social Circle, GA Quality Validation Associate I Bachelor's degree in science, engineering or other related technical field Exp: 1+ years |
This position supports site projects, technical transfers, and ongoing validation maintenance. Primarily responsible for compliance during the review of the design, authorship, and execution of commissioning, qualification. This position is responsible to maintain validation documentation aligned with Good Documentation Practices (GDP) and ensure compliance with industry standards (e.g. FDA, EU GMP, ISO, etc). Provides technical subject matter expert (SME) support to change controls, investigations, deviations, and CAPAs. Individual must work on moderate to complex assignments, where analysis of situations or data requires an in-depth evaluation of various factors or intangible variables. | 06/18/2025 |
| 1082 | Tempus Chicago, IL Molecular Technologist I (Extractions) BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 0-1+ years |
Work with a cutting-edge genomics workflow to provide high-quality data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform nucleic acid extraction and DNA/RNA quantification and qualification using robotics and automated liquid handlers. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 06/18/2025 |
| 1083 | Tempus Chicago, IL Quality Control Technologist I BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work within a cutting-edge genomics workflow to provide quality control support in a high-volume clinical molecular laboratory. Help create and implement new equipment functionality for use by Tempus R&D and clinical lab staff while maintaining CLIA/CAP/NYS-DOH/ISO compliance. Complete Performance Qualifications (PQs), Preventive Maintenance (PM), relocation, and routine maintenance for all clinically approved molecular laboratory equipment. Collect and help analyze metrics. Investigate equipment related issues and help facilitate and implement corrective and preventative actions. Interact with lab management and personnel to provide training, troubleshoot issues, and prioritize QC tasks. Report significant findings/deviations and system deficiencies to lab management, as appropriate. Update SOPs and equipment records within the document control system, including creation/ revision/ review of internal SOPs and other quality documentation. Create and review protocols and qualification summaries. Support the Lab QC team with reagent and documentation tasks as needed. Monitor and respond to laboratory temperature excursions. | 06/18/2025 |
| 1084 | PTC Therapeutics Mountain View, CA Contract, Lab Technician, Biology B.S. in chemistry, biochemistry or biology Exp: 0-2 years |
The Contract, Lab Technician, Biology will aid in the management of the proprietary compound collection at the PTC Mountain View Research Site. This individual will be a key member of the research group, providing samples to internal and external collaborators. Additionally, the compound management technician will perform routine chemical and biological assays to support various programs. The successful candidate will be almost pathologically detail-oriented and thrive performing high precision work. The Contract, Lab Technician, Biology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. | 06/10/2025 |
| 1085 | PTC Therapeutics Bridgewater, NJ Associate Scientist I, Biology (Biochemistry) Master’s degree in a scientific discipline Exp: 1-2 years |
The Associate Scientist I, Biology (Biochemistry) is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. The Associate Scientist I, Biology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. | 06/10/2025 |
| 1086 | Purdue Pharma Wilson, NC Quality Specialist II, Chemist Raw Materials MS in Chemistry or closely related science Exp: 1 year |
Performs a variety of chemical analyses and GMP review of raw materials, packaging components, ancillary solutions, in-process samples, finished product and stability samples in accordance with cGMP, GLP, DEA and company policies and procedures. Assists in writing and performing method validations and method transfers. Assists in process validations. Conducts equipment validations IQs, OQs, PQs, and MQs, if necessary. Provides assistance and technical support to other groups with chemical testing needs and performs troubleshooting of analytical methods and instrumentation. | 06/10/2025 |
| 1087 | Purdue Pharma Wilson, NC Quality Specialist I, Chemist BA or BS degree in Chemistry or closely related science Exp: 6 months |
The Quality Specialist I, Chemist is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing and GMP review in support of the analysis of raw materials, packaging components, ancillary solutions, in-process samples, finished product method development and/or transfers, cleaning/process validations, and stability samples. Will follow standard procedures in accordance with cGMP, GLP, DEA and company policies and procedures. | 06/10/2025 |
| 1088 | QIAGEN Germantown, MD Metrology Technician BS/BA Exp: 1-3 years |
The Metrology Technician performs equipment calibration assignments using standard methods and processes. Required duties include: Set-up, calibration, testing, repair, inspection and maintenance of equipment and tools. Making adjustments, modifications or replacements as needed. Maintain and document calibration of all measurement equipment (in the Electronic Calibration Maintenance Management System). Creating, maintaining, and updating department SOPs and other documentation as required. Coordinate the execution of the calibration program to include event scheduling, performance, and oversight of service suppliers. Provide notification of calibration tasks with due dates. Coordinate calibration scheduling with equipment owners when needed. Oversee work by outside calibration contractors to ensure compliance with applicable procedures. Troubleshoots and solves calibration and maintenance problems of moderate scope and complexity requiring broad technical interpretation of defined procedures and practices. Responsible for ensuring on-going compliance to applicable quality and EHS regulations and standards (e.g., cGMP, FDA, ISO, IVDD, OSHA, etc.). | 06/10/2025 |
| 1089 | Quality Agents , MD Quality Assurance Specialist BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Quality Assurance Specialists are leading service providers to our clients providing GMP support. The individual will coordinate validation activities with the client and meet timelines. | 06/10/2025 |
| 1090 | Quality Agents Rockville, MD Validation Engineer I BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by the client. | 06/10/2025 |
| 1091 | Quansys Biosciences West Logan, UT Formulation Specialist I Bachelor’s degree in Biology, Chemistry, Biotechnology, or related field Exp: 0-2 years |
A Production Associate I is responsible for meeting production schedules in a fast-paced, high throughput industrial setting. This may include the production immunoassay components, chemical buffers, biological diluents/reagents, coated plates, and/or assembled kits, for customer order fulfillment. They will be responsible, under supervision, to follow established SOPs in order to support the goals of the department. Some degree of professional latitude, creativity and self management is expected. This position may manage very specific aspects of the manufacturing process within the department. | 06/10/2025 |
| 1092 | Quansys Biosciences West Logan, UT Research Associate I Bachelor’s degree in life sciences, cellular and molecular biology, protein sciences or related field Exp: 1+ years |
A Research Associate I (RA I) is responsible for carrying out reagent and assay development activities in the laboratory, under supervision, working to achieve development project goals including data analysis and assay qualification. This is a laboratory position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). Some degree of professional latitude, creativity and self management is expected. | 06/10/2025 |
| 1093 | QuidelOrtho Rochester, NY V&V Engineer I (R&D) B.S. Degree in Computer Science, Chemistry, Biochemistry, Biology, Engineering, or a related discipline Exp: 1-2 years |
As QuidelOrtho continues to grow, we are seeking a Verification and Validation Engineer I to help with formal verification and validation of complex medical devices under the regulations of the FDA. The individual will be part of an engineering team that is responsible for requirements based test design and execution of test procedures both in a virtual and lab environment. The team is highly collaborative and will require regular interactions in formal reviews, test planning activities, and working with software development to reproduce and verify system defects. | 06/10/2025 |
| 1094 | Quva Bloomsbury, NJ Microbiologist I - 1st Shift Bachelor’s Degree, Biology discipline Exp: 0-2 years |
Our Microbiologist I plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete training, you will be required to perform individual hands-on work in the sterility testing and/or endotoxin testing programs. This person provides scientific guidance and interpretation of microbiology results to QC and production management. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. | 06/10/2025 |
| 1095 | Reckitt St. Peters, MO Quality Compliance Associate B.S. degree in a science field preferably Chemistry Exp: 1-3 years |
Perform chemical and/or physical testing on all in-process, finished, validation, and R&D products according to applicable procedures while following all relevant laboratory Test Methods, SOPs, etc. Provide support for or perform calibration, laboratory investigations, and projects as required. Participate in advanced training on equipment and/or methods and assist as needed in validation and method development. | 06/10/2025 |
| 1096 | Regeneron Tarrytown, NY Sr Assoc Scientist - Immunology and Inflammation BS/MS Exp: 1-4 years |
Regeneron's Immunology and Inflammation group, located in Tarrytown, NY is looking for an energetic Sr Associate Scientist to join a highly collaborative team working in autoimmunity and/or allergy, B cell biology and disease models driven by pathogenic antibodies. | 06/10/2025 |
| 1097 | REGENXBIO Rockville, MD Clinical Research Associate Bachelors degree required; scientific discipline or related healthcare field Exp: 1 year |
As a Clinical Research Associate (CRA), you will be responsible for the support and coordination of the logistical aspects of clinical trial management, site management, data review & cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs. You’ll act as a pivotal point of contact for the clinical trial team and assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. | 06/10/2025 |
| 1098 | REGENXBIO Rockville, MD Sr. Clinical Trial Associate Bachelor's degree required preferably in a scientific discipline or related healthcare field Exp: 1-2 years |
As a Senior Clinical Trial Associate, you will be responsible for coordinating the logistical aspects of clinical trials and electronic Trial Master File (eTMF) support according to Good Clinical Practice (GCP) and relevant SOP’s. You’ll act as a pivotal point of contact for the clinical trial team and assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. | 06/10/2025 |
| 1099 | REGENXBIO Rockville, MD Associate Clinical Sample Manager Bachelor's degree required preferably in a scientific discipline or related healthcare field Exp: 1-2 years |
REGENXBIO is an exceptional place where some of the best of brightest people have the opportunity to collaborate, touch amazing science, and contribute toward extraordinary plans. As a Contract Associate Clinical Sample Manager, you will be provide support and coordination of the logistical aspects of clinical sample management which includes coordinating operational activities required to collect, track, and deliver clinical trial samples for all assigned clinical trials. You’ll also support the management of vendor contracts as applicable. This is a 6-month contract position with the potential to convert to permanent. | 06/10/2025 |
| 1100 | Repertoire Immune Medicines Cambridge, MA Research Associate I Bachelor’s or master’s degree (or equivalent) in scientific discipline or a health-related field Exp: 1+ years |
We are seeking a Research Associate to join our Platform Discovery Team. Some of the primary responsibilities of the RA will include preparation of in-house reagents required for our DECODE platform as well as the execution of next-generation sequencing experiments as well as downstream quality control. These activities will be performed both manually at the bench as well as with the help of liquid handling instrumentation. We are looking for an enthusiastic team player who will thrive in a fast-paced, dynamic, and highly collaborative environment. The RA will work as part of a cross-functional team of immunologists, molecular biologists, and protein scientists to successfully execute experiments and contribute to process optimization. This is a temporary, 6-month contract position. | 06/10/2025 |
| 1101 | Revolution Medicines Redwood City, CA Clinical Trial Assistant II Bachelor’s degree in biological sciences or related health related field Exp: 1-3 years |
As a Clinical Trial Assistant II in Clinical Operations, initially reporting to the Director Clinical Operations, you will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support RevMed clinical trials. | 06/10/2025 |
| 1102 | Revolution Medicines Redwood City, CA Clinical Trial Assistant II, Clinical Operations Process & Systems Bachelor’s degree in biological sciences or health-related field Exp: 1-3 years |
This is a unique opportunity for a Clinical Operations Professional. As the Clinical Trial Assistant II (CTA II), Clinical Operations Process and Systems, you will be responsible for acting as an integral member of the Clinical Operational Strategy & Process Optimization team and will be tasked to support the management of Clinical Operations processes and systems, in support of Clinical Operations and execution of RevMed’s clinical trials. | 06/10/2025 |
| 1103 | RION Rochester, MN Research Associate Bachelor’s or Master’s degree with focus in Biological Sciences Exp: 1+ years |
The Research Associate will contribute to ongoing scientific projects within the Research and Development laboratory focused on Rion’s exosome technology. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, flow cytometry, ELISA, RT-qPCR, and colorimetric/fluorometric-based assays. The Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Research Associate will work closely with the Research and Development Scientists and support the efforts Process Development. As such, the successful candidate will work in an upbeat, highly collaborative and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 06/10/2025 |
| 1104 | Roche Nashville-Davidson, TN Field Engineering Specialist Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem-solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1105 | Roche Salt Lake City, UT Field Engineering Specialist Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1106 | Roche Providence, RI Field Engineering Specialist- Molecular Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. This role offers the opportunity to support our serology business, which plays a critical role in detecting antibodies and antigens to aid in diagnosing infections, ensuring blood safety, and monitoring immune responses | 06/10/2025 |
| 1107 | Roche Springfield, MA Field Engineering Specialist Bachelor's degree in a relevant field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem-solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1108 | Roche Philadelphia, PA Lab Associate, Laboratory Operations BA/BS in biological sciences Exp: 0-3 years |
Support the day-to-day laboratory activities across Roche's Research and Technology facilities. Provide a safe and efficient workspace for scientific activities in close collaboration with the scientific laboratory staff, facilities, and inventory management personnel. | 06/10/2025 |
| 1109 | Roche Cincinnati, OH Field Engineering Specialist Bachelor's degree in a relevant field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem-solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1110 | Roche Boston, MA Field Engineering Specialist Bachelor's degree in a relevant field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1111 | RoslinCT Hopkinton, MA Cell Processing Associate (3rd Shift) Bachelor's degree in biology or related scientific discipline Exp: 0-5 years |
This is a third shift role reporting to the Manufacturing Supervisor. The position's core responsibilities are focused on clinical and commercial manufacturing processes related to cell therapies. Activities include aseptic sampling of products in a Grade A environment, to operate automated, single-use systems for the targeting, expansion, and harvesting. Operate and maintain cell processing equipment. The Cell Processing Associate will support inventory management, suite cleaning, and setup activities per RoslinCT’s governing procedures. This position may require the individual to collaborate as needed with peers within Manufacturing Sciences and Technology (MS&T), Quality, and Facilities. | 06/10/2025 |
| 1112 | RoslinCT Hopkinton, MA QC Analyst II, Microbiology (3rd Shift) Bachelor's Degree in scientific discipline, Microbiology focus Exp: 0-7+ years |
The Quality Control Microbiology, QC Analyst will be responsible for collecting environmental samples in clean room areas to support manufacturing operations, sample management activities, and testing of cell therapy in-process and release product samples. The person will be responsible for reporting data and writing/revising standard operating procedures (SOPs) and test methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Microbiology will partner with the QC analytical team, interface with multiple groups including manufacturing, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 06/10/2025 |
| 1113 | RoslinCT Hopkinton, MA QC Analyst I/II, Analytical (3rd Shift) Bachelor's Degree in scientific discipline Exp: 0-5+ years |
The Quality Control Analytical, QC Analyst will be executing analytical methods such as appearance, pH, osmolality, cell counting, ELISAs, flow cytometry and related methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Analytical will partner with the analytical team, interface with multiple groups, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. He/she will be responsible for authoring Standard Operating Procedures (SOPs), specifications and Test Methods. He/she will assist in the implementation of new assay methodologies and the associated instrumentation. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 06/10/2025 |
| 1114 | RoslinCT Hopkinton, MA QC Analyst I/II, Analytical Bachelor's Degree in scientific discipline Exp: 0-5+ years |
The Quality Control Analytical, QC Analyst will be executing analytical methods such as appearance, pH, osmolality, cell counting, ELISAs, flow cytometry and related methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Analytical will partner with the analytical team, interface with multiple groups, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. He/she will be responsible for authoring Standard Operating Procedures (SOPs), specifications and Test Methods. He/she will assist in the implementation of new assay methodologies and the associated instrumentation. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 06/10/2025 |
| 1115 | RoslinCT Hopkinton, MA QC Analyst, Microbiology Bachelor's degree in scientific discipline Exp: 0-7+ years |
The Quality Control Analyst will be responsible for collection of environmental and raw material samples, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. | 06/10/2025 |
| 1116 | Sai Life Sciences Watertown, MA Research Associate - Biology Bachelor's or Master's degree in Biology Exp: 1+ years |
As the Research Associate in Biology, you will play a crucial role in conducting groundbreaking research, contributing to our mission of advancing scientific knowledge and addressing pressing biological challenges. Working closely with our team of scientists, you will be involved in various aspects of experimental design, data collection, analysis, and interpretation. This position offers an exciting opportunity to be at the forefront of scientific discovery and make a meaningful impact in the field of biology. | 06/10/2025 |
| 1117 | Sai Life Sciences Watertown, MA Senior Research Associate - Biology Master's degree in Biology Exp: 1+ years |
As the Senior Research Associate in Biology, you will play a crucial role in conducting groundbreaking research, contributing to our mission of advancing scientific knowledge and addressing pressing biological challenges. Working closely with our team of scientists, you will be involved in various aspects of experimental design, data collection, analysis, and interpretation. This position offers an exciting opportunity to be at the forefront of scientific discovery and make a meaningful impact in the field of biology. You’ll have the opportunity to develop your skills to work independently and advance your knowledge-base on assay development and optimization. | 06/10/2025 |
| 1118 | Sanguine Biosciences Remote, Research Coordinator I, Translational Bachelor's Degree in a life science or other related field Exp: 1-2 years |
The role of the Research Coordinator I, Translational is to serve as a primary point of contact for potential donors in research studies and maintain all associated participant data. The Research Coordinator I is responsible for screening and qualifying donors who are part of an extensive Sanguine database, and those who are identified by the Patient Recruitment and Marketing Team. The Research Coordinator I will screen potential donors to obtain the necessary health information, and conduct medical record reviews to qualify donors for research studies. The Research Coordinator I may also have the opportunity to work on specific aspects of clinical trials and other research study types, as it relates to patient data, appointments and compliance. This role will work cross functionally with multiple departments including Project Management, Field Operations, and Apheresis Operations. This role will report to the Patient Operations Manager and will be a part of a service-centric and analytics-driven team that believes in empathy, compassion, and centering our focus on the needs of our donors. | 06/10/2025 |
| 1119 | Sanofi Waltham, MA Senior Research Associate, BioAnalytics (Biophysics) M.S. degree in Analytical Chemistry, Biochemistry, or related discipline Exp: 0-2 years |
We are seeking a motivated senior research associate to join our BioAnalytics Characterization group in the Genomic Medicine Unit within Sanofi. The Genomic Medicine Unit at Sanofi is dedicated to the establishment of best-in-class platforms to support development of life-changing advanced gene therapy products, including recombinant AAV vectors and lipid nanoparticles. The BioAnalytics Characterization group uses advanced analytical techniques for in-depth structural and functional characterization of gene therapy products in support of drug development, from pre-candidate selection through commercialization. | 06/10/2025 |
| 1120 | Sanofi Ridgefield, NJ Aseptic Technician II Bachelor's degree Exp: 1+ years |
Prefilled Syringe (PFS) Manufacturing is responsible for fill and finish of prefilled syringe products produced on the site. This includes hyaluronic acid (HA) based medical device products as well as pharmaceutical based products. In support of our main functions, additional responsibilities include cleaning and sanitization of process equipment. Based on production schedules, random and different start time scenarios may occur, so a very flexible work schedule is required for the candidate. Ability to accommodate production requirements that may require 50+ hour workweeks, including 2nd shift or split shift hours, extended day hours and weekends. This role requires frequent work on weekends depending on production demands. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? | 06/10/2025 |
| 1121 | Sanofi Pearl River, NY Quality Control Support Professional Bachelor's science degree ( Biochemistry, Chemistry, Biology, Molecular Biology, Immunology and or related disciplines) Exp: 1-2 years |
The role involves supporting quality control and project management at the Pearl River site, ensuring compliance with regulatory standards for environmental and microbiological contamination control. | 06/10/2025 |
| 1122 | Saptalis Hauppauge, NY Analytical Scientist B.S/M.S in Analytical Chemistry or related discipline Exp: 0-2 years |
Saptalis is looking to recruit Analytical Scientists to join the growing Analytical R&D group at our facility in Hauppauge, NY. Analytical Scientist is responsible for developing and validating analytical methods for analytes of interest in new drug products using UPLC, HPLC, GC and other analytical instruments. Execute all functions in accordance with current FDA regulations, ICH guide lines, USP methodologies, cGLPs and Saptalis SOPs. | 06/10/2025 |
| 1123 | Saptalis Hauppauge, NY Quality Control Scientist BS/MS Degree (chemistry or related field) Exp: 0-2 years |
Saptalis is looking to recruit QC Scientists to join the growing Quality group at our facility in Hauppauge, NY. QC Scientist is responsible for GMP testing of raw materials, in-process, finished product and stability samples for release. In addition, the responsibilities include maintaining laboratory equipment, assisting in investigations and coordinating external testing as needed. | 06/10/2025 |
| 1124 | Outpace Bio Seattle, WA Research Associate II/Senior Research Associate, Analytical Development M.S. in Biology, Biochemistry, Immunology, Molecular Biology, Analytical Chemistry, Biotechnology, or related disciplines Exp: 0-2+ years |
Outpace Bio is seeking an Research Associate II/Senior Research Associate to support development of analytical assays and technology transfer to CDMO partners for the GMP production of lentiviral vectors and CAR/TCR drug products. As a member of the Technical Operations team, the Research Associate II/Senior Research Associate will contribute to analytical development projects supporting CMC activities, authoring analytical development reports, advancing early phase analytical method transfer from the Outpace R&D team, and conducting hands-on, technical laboratory work. This position will report to the Senior Scientist, Analytical Development and will work closely with R&D functional groups (Platform, Immunology, CAR T development) as an integral part of project teams. Key contributions expected from this role include novel assay development, support for internal process and assay technology transfer to CDMOs and CROs, communications to internal and external stakeholders, and providing necessary technical support for regulatory submissions. | 06/03/2025 |
| 1125 | Padagis Minneapolis, MN Senior Quality Control Chemistry Testing Technician Bachelor's degree Exp: 1+ years |
We are hiring for multiple positions for QC Chemistry Technician II, 1st Shift, in New Hope, MN who performs inspection on a range of work to detect defects and maintain quality standards. who performs inspection on a range of work to detect defects and maintain quality standards. | 06/03/2025 |
| 1126 | Padagis Minneapolis, MN Senior Microbiology Testing Technician, Quality Control Bachelor of Science in Microbiology or related science Exp: 1+ years |
We are hiring for multiple Microbiologist II Technicians to support the Microbiological analysis of products, stability samples, validation samples, raw materials, and environmental samples through testing, data analysis/interpretation, method validation and continuous improvement projects. | 06/03/2025 |
| 1127 | Parexel West Point, PA Scientist III - Biophysical & Materials Analytical Characterization MS in chemistry, biology, or related field Exp: 1-2 years |
This is a laboratory-based scientific role in a fast-paced, multidisciplinary team environment, requiring the utilization of biophysical analytical characterization techniques to support development of vaccine drug substance and drug products in a GMP-like environment. The vaccine drug substance and product development support includes sample manipulation, equipment maintenance, routine analysis, and characterization of development vaccines to support process and formulation development. | 06/03/2025 |
| 1128 | Parexel West Point, PA Scientist II or III - Device Verification Scientist - FSP B.S. or M.S. Degree in Automated Sciences, Engineering, Chemistry, Biology or equivalent Exp: Scientist 2 - BS: 1-2 years or MS: 1+ years Scientist 3 - MS: 1-2 years |
We are looking to fill a Scientist 2 or 3- Device Verification Scientist position working as a full-time employee of Parexel on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. The Center for Packaging and Device Analytics (CPDA) provides physical analytical expertise in support of production and commercialization of packaging and combination device products. | 06/03/2025 |
| 1129 | Parexel Rahway, NJ Scientist II or III - Automation / Robotics Scientist MS or BS degree in chemical engineering, chemistry, biochemical engineering, or related applied science field Exp: Scientist 2 - BS: 1-2 years or MS: No Exp Scientist 3 - MS: 1-2 years |
We are looking to fill a position for a Scientist working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. | 06/03/2025 |
| 1130 | Parexel Rahway, NJ Scientist II or III - HPLC Separations Focus - FSP BS or MS Exp: Scientist 2 - BS: 1-2 years or MS: 0-1 years Scientist 3 - MS: 1-2 years |
We are looking to fill a position for a Scientist working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. | 06/03/2025 |
| 1131 | Parexel Rahway, NJ Engineer III - API Crystallization - FSP MS degree or equivalent in Engineering, Chemistry, Chemical Engineering, or a related field is required Exp: 1-2 years |
The Chemical Engineering Research and Development department of one of our clients in Rahway, NJ has a position available that will have primary accountability for lab process development specifically around API crystallization, isolation, drying, and particle physical attribute control. Activities will include working with gram quantities at the bench scale to a few kilograms at the Unit Operations and Preplab scales utilizing wet and dry processing equipment within these labs (e.g., crystallization vessels, filtration and drying equipment, and wet and dry milling tools, etc.). The department offers fast-paced, hands-on research that requires a high degree of technical skills and contributions. Secondary activities may include experiments and the use of instruments associated with process safety evaluation when needed, and the general support of Specialty Labs operations within the Chemical Engineering R&D Department. | 06/03/2025 |
| 1132 | Parexel West Point, PA Scientist III - Process Development & Characterization Support M.S. in Chemistry, Biology or similar life sciences Exp: 1-2 years |
We are looking to fill a Scientist III - Process Development and Characterization Support position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. Support of standard analytical testing of samples from vaccines and large molecule process development/characterization. Other potential opportunities include method development/optimization. | 06/03/2025 |
| 1133 | Parexel Rahway, NJ Scientist III - Analytical Chemist - FSP M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology or similar life sciences Exp: 1-2 years |
We are looking to fill a Scientist 3 –Analytical Chemist (Raw Materials) position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. The position does not offer any sponsorship. Conduct raw materials release testing, and cleaning validation and cleaning verification testing, using a myriad of methodologies and techniques including separations sciences in a GMP laboratory. | 06/03/2025 |
| 1134 | PCI Rockford, IL Operations Process Engineer Bachelor's Degree in a related field Exp: 1-5 years |
This position will work to continuously improve processes and systems that ultimately lead to improved profitability to the company. Using all available Engineering, Lean, and Six Sigma tools, this position will work independently and cross-functionally to drive out waste and reduce process variability. | 06/03/2025 |
| 1135 | PCI San Diego, CA Quality Compliance Specialist Bachelor's Degree in a related field Exp: 1-5 years |
The Quality Compliance Specialist supports the site compliance and regulatory strategies necessary to support customer’s products as well as leading both regulatory inspections and customer audits. They are responsible for supporting the implementation of company policies and objectives involving matters of government and regulations, with respect to the FDA, DEA, and other ex-US regulatory agencies as applicable. The role will also provide support for client business reviews, investigations, complaints, CAPAs, inspections, quality metrics, and continuous improvement initiatives as required by the company supervisory responsibilities for the role. | 06/03/2025 |
| 1136 | Penumbra Alameda, CA Manufacturing Engineer I - Development Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 06/03/2025 |
| 1137 | Penumbra Roseville, CA Manufacturing Engineer I - Metals Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 06/03/2025 |
| 1138 | Penumbra Roseville, CA Manufacturing Engineer I -Catheters Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 06/03/2025 |
| 1139 | Penumbra Roseville, CA Quality Engineer I Bachelor’s or Master's degree in an engineering or scientific discipline Exp: 1+ years |
As a Quality Engineer I, you will be charged with the quality behind Penumbra's game-changing medical devices used to address some of the world's toughest disease states! Unlike quality engineering roles in other companies, at Penumbra, we provide our quality engineers with highly technical problems to solve. Your efforts will directly impact the safety of patients around the world who use our products. You will apply your passion for creative problem solving throughout all stages of the process, from concept to commercialization and into continuous improvements. | 06/03/2025 |
| 1140 | Perrigo Holland, MI Validation Engineer I Bachelor's degree in Engineering, Chemistry, Pharmacy or a closely allied field Exp: 1 year |
Perrigo is now hiring for a Validation Engineer who will work out of our facilities in Holland, Michigan. The Validation Engineer will primarily be responsible for preparing and reviewing plans, protocols, reports, and studies associated with validation activities (Process, Packaging, Cleaning, and Equipment). | 06/03/2025 |
| 1141 | Personalis Fremont, CA Clinical Lab Associate 1, Sun-Th AM Shift BA/BS in a biological discipline Exp: 0-2 years |
At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. | 06/03/2025 |
| 1142 | Personalis Fremont, CA Clinical Lab Associate 1, Th-M AM Shift BA/BS in a biological discipline Exp: 0-2 years |
At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. | 06/03/2025 |
| 1143 | Personalis Fremont, CA Clinical Lab Associate 1, Tu-Sat AM Shift BA/BS in a biological discipline Exp: 0-2 years |
At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. | 06/03/2025 |
| 1144 | Pfizer Sanford, NC Sr. Associate Scientist, QC Chemistry Bachelor's degree Exp: 0+ years |
The position will support the Pfizer Sanford, NC Quality Operations department by performing Quality Control activities associated with clinical and/or commercial product, raw materials, and validation. Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; testing, analyzing, interpreting, and trending results; and creating, reviewing and approving documentation. Individual should have knowledge of current Good Manufacturing Practices (cGMP), Laboratory Information Management System (LIMS), Microsoft Office™ applications specifically Word and Excel, analytical techniques and instrumentation, Lean Six Sigma concepts, and Lean Labs. | 06/03/2025 |
| 1145 | Pii Hunt Valley, MD QMS Associate Bachelor's degree Exp: 1-2 years |
The QA Associate ensures compliance with CGMP and internal policies, procedures, and specifications. This position is responsible for performing a role in any one or more of the following functions: Quality Operations, Process Quality, Batch Release, Quality Management Systems, and Compliance in accordance with CGMP and related company SOPs, state, federal and local laws as applicable. | 06/03/2025 |
| 1146 | Pii Hunt Valley, MD Microbiologist (EM) B.S / M.S. in a life sciences discipline Exp: 0-2 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions. | 06/03/2025 |
| 1147 | Quest Diagnostics Lenexa, KS Forensic Toxicology Laboratory Scientist I Bachelor’s Degree Exp: 1 year |
This position works within the Forensic Toxicology Laboratory and is responsible for all aspects of testing of donor specimens including specimen preparation and instrument operation. | 06/03/2025 |
| 1148 | Quest Diagnostics Chantilly, VA Sr. Associate Scientist (R&D Toxicology) MS degree in Engineering, Chemistry, Chemical Engineering, or a related field is required Exp: 1-3 years |
Participates on a team of scientists in the development and transfer of assays. Incumbent will work in the laboratory. | 06/03/2025 |
| 1149 | Quest Diagnostics Chantilly, VA Associate Scientist, Toxicology (LCMS) - Hybrid Master's degree Exp: 1 year |
Participates on a team of scientists in the development and transfer to manufacturing of processes to purify, characterize and modify enzymes, antibodies and other proteins. Candidate will be expected to work in the laboratory. | 06/03/2025 |
| 1150 | Pledge Therapeutics Canton, MA Research Associate, Immuno-Oncology MS Exp: 1-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our new state-of-the-art facility in Canton, MA. The successful candidate will engage in the Immuno Oncology research areas of the company and will work with a successful team of international senior scientists located in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 06/03/2025 |
| 1151 | Pledge Therapeutics Canton, MA Research Associate, Virology Bachelor’s or Master’s degree in biological sciences or a related field Exp: 0-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our state-of-the-art facility in Canton, MA. The successful candidate will engage in the company’s virology research areas and work with a successful team of scientists in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 06/03/2025 |
| 1152 | Thermo Fisher Chantilly, VA Field Service Engineer II (LCMS) Bachelor’s Degree in Sciences, Engineering, Electronics Exp: 1-3 years |
This role sits within our Unity Lab Service (ULS) organization, which provides a single source for integrated lab service, support, and supply management. Our customized service offerings and outstanding services have the flexibility and experience to uniquely address our customer’s business needs. Whether they are looking to arrange for service on a single instrument or are seeking resources to handle entire labs, there is a solution to meet their business requirements. | 06/03/2025 |
| 1153 | Thermo Fisher Chelmsford, MA Scientist II, Manufacturing Sciences M.Sc. in Chemistry or chemical engineering Exp: 1-3 years |
The Scientist II will make an impact by driving raw material second-sourcing projects, including conducting characterization studies and bench builds. Perform characterization studies and analyze organic or inorganic compounds, raw materials, and finished products. Execute bench experiments effectively and develop polymer products and related processes to meet performance specifications. | 06/03/2025 |
| 1154 | Thermo Fisher Chicago, IL Scientist - HPLC, GMP Masters degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology Exp: 0-2 years |
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. | 06/03/2025 |
| 1155 | Thermo Fisher Greenville, NC Sr Formulation Technician: Control Room & Lyophilizer Bachelor’s Exp: No exp |
The Sr. Formulation Technician will be able to perform tasks with little to no direction. They will provide guidance in the absence of the Lead Formulation Technician. They will be proficient in aseptic filling and manufacturing. This colleague follows written and verbal instructions using cGMP documents and operating equipment when performing the following duties. Shift hours are 6am-6pm on a 2-2-3 rotating schedule. | 06/03/2025 |
| 1156 | Thermo Fisher Richmond, VA Assistant Scientist Bachelor's degree (chemistry, biology, biochemistry, microbiology or similar life science degree) Exp: 0-1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 06/03/2025 |
| 1157 | Thermo Fisher Sunnyvale, CA Scientist I, Manufacturing Sciences Bachelor’s degree or higher in Chemistry Exp: 0-1 years |
The Scientist I, Manufacturing Sciences, will be responsible for the synthesis of functionalized resins used in columns. | 06/03/2025 |
| 1158 | Thermo Fisher Wilmington, DE Associate Scientist, Formulations Bachelor's degree in Biological Sciences, or other related degree concentration Exp: 1-2 years |
The associate scientist will perform a variety of routine to complex lab activities related to formulation and overall drug product development of large molecule drug products. The role involves designing and executing the experiments, document experimental details, organize the data, and summarize the findings in a technical summary report. The position emphasizes scientific rigor, collaboration with different functions, and effective communication of findings within the organization. | 06/03/2025 |
| 1159 | PROCEPT BioRobotics San Jose, CA Associate Equipment Engineer BS in an Engineering discipline such as mechanical, Biomedical, or electrical engineering Exp: 6 months |
Are you ready to embark on an exciting journey that will revolutionize the way men suffering from BPH are treated? Join us as Director of Manufacturing Engineering and be at the forefront of producing a best-in-class therapy and technology that promises to become the standard of care for BPH. Your mission? Lead the Manufacturing Engineering team for Capital Equipment in both sustaining and improving the production operation for the Hydros and Aquabeam robotic systems but also supporting new product introduction for the next generation systems and all future Capital Equipment. This isn't just any job - it's a chance to make a real difference. We need a technical leader with the vision to guide production operations larger scale and capacity while maximizing the quality and performance of every system produced. We are looking for someone with the leadership skills to create a premier engineering team and build a cross-functional team dynamic that optimizes development and operational speed with a product quality unmatched in the space. Vision, technical acumen, high energy, communication, integrity and honesty will all be needed to succeed in this role and what we value at Procept. Get ready to transform lives and shape the future of healthcare! | 06/03/2025 |
| 1160 | Proclinical Cambridge, MA Quality Assurance Specialist Bachelor's degree in a scientific discipline (e.g., Biology, Chemistry, Engineering) Exp: 1-3 years |
We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world. The successful candidate will focus on document management and quality operations within the cardiovascular pharmaceuticals sector. Your expertise will support continuous improvement initiatives and ensure compliance with industry standards. | 06/03/2025 |
| 1161 | PSC Biotech York, PA QC Analyst I Bachelor’s degree in related science discipline, i.e. Chemistry, Microbiology. Exp: 1-3 years |
We are hiring an entry-junior level QC Analyst I. The QC Analyst I will be responsible for conducting quality control testing in the and ensuring the safety, efficacy, and consistency of products. This role involves rigorous analysis at every stage to ensure compliance with regulatory standards and internal quality guidelines. | 06/03/2025 |
| 1162 | PSC Biotech Remote, Validation Engineer I Bachelor's degree in related engineering discipline Exp: Entry Level |
This position will support system validation and product release processes, ensuring compliance with industry standards and regulatory requirements. You will play a key role in contributing to the development and improvement of validation procedures and driving overall product excellence. This is an entry-level, remote position. Successful candidates have a bachelor’s degree within an engineering discipline, a passion for technology, and exposure to system/software testing in the life science industry. | 06/03/2025 |
| 1163 | PSC Biotech York, PA Metrology Technician I Bachelor's degree in engineering or related technical field Exp: 0-1 years |
We are hiring an entry to junior level Metrology Technician responsible for conducting routine calibration tasks in alignment with established protocols and regulatory mandates. The position adeptly handles troubleshooting and equipment repair as needed, while ensuring the steadfast adherence to quality system compliance standards. | 06/03/2025 |
| 1164 | Natera Austin, TX QC Reagent Assoc 1 BS/BA degree (or equivalent) in Biological Sciences, Biology, Chemistry or a related field Exp: 1+ years |
Support the activities for reagents used in the Operations Department’s Clinical Laboratories. Executes the preparation and qualification of molecular diagnostic reagents. Performs Quality Control tests on new incoming shipments of raw materials and small-scale manufacturing procedures (formulations and dispensing) reagent. Reviews data obtained for compliance to specifications and reports abnormalities. Maintains and improves QC documentation pertaining to raw material specification, reagent qualification, and QC testing. Support Incoming Quality Control activities as needed. | 05/28/2025 |
| 1165 | Natera San Carlos, CA Senior Service Engineer BS/BA in a biological science/biomedical engineering, similar field of study Exp: 1-3 years |
The Instrument Support Engineer is responsible for the service and support of laboratory equipment and instrumentation utilized in the Operations laboratory. The scope of support includes installation, calibration, maintenance, and repair of both simple (e.g., plate sealers) and complex (e.g., liquid handling robotics) instrumentation in the laboratory. The Instrument Service Engineer will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. | 05/28/2025 |
| 1166 | Natera San Carlos, CA Research Associate BS/BA in a biological science or equivalent Exp: 1-2 years |
The Research Associate 1, performs laboratory procedures of varying complexity contributing to cross functional activities as part of the Sample Processing team. Works primarily with R&D Scientific Operations, a multidisciplinary team within the research and development department. | 05/28/2025 |
| 1167 | Natera Austin, TX Research Associate 1 Bachelor’s degree in Biological Sciences, Biotechnology, Molecular Biology, or a related field Exp: 0-2 years |
We are seeking a highly motivated and skilled Research Associate 1 to join our dynamic team in sample management. In this role, you will be responsible for the management of biological samples, ensuring their integrity, overseeing quality control, and supporting research projects that rely on biological specimens. The ideal candidate should have a strong background in bio-sample management, research methodologies, and data analysis, with an interest in contributing to cutting-edge scientific research. | 05/28/2025 |
| 1168 | Neuralink Austin, TX Mechanical Engineer, Surgery Engineering Bachelors Degree in Mechanical Engineering or Industrial Engineering Exp: 1-3 years |
The Surgery Engineering team is responsible for developing and managing custom hardware and processes for neurosurgical procedures, excluding the R1 Robot and Operator Station. Their responsibilities encompass the entire surgical process, including patient positioning, incision management, craniectomy, precise implant placement, thread management during robot-assisted insertion, surgical site irrigation, implant installation, and closure. Additionally, the team ensures safe explantation and upgrade procedures for implants. They also provide mechanical engineering support to the animal care, histology, and BCI teams, contributing to the success of complex neurosurgical procedures and related research activities. | 05/28/2025 |
| 1169 | Neurocrine Biosciences San Diego, CA TEMP - Associate Scientist / Scientist, Biologics Characterization, Biologics Lead Optimization Bachelor's degree in relevant scientific discipline Exp: 1-5+ years |
We are in search of a collaborative, passionate scientist with sound scientific knowledge and excellent technical skills in cell-based in-vitro assays, molecular biology and analytical sciences for AAV gene therapy and biologics. In the biologics lead optimization team, you will be responsible for performing routine analytical tests and developing/optimizing analytical methods to support the development and manufacturing of AAV based gene therapy products and biologic therapeutics. In this role, you will collaborate across multiple groups including process development, CMC, research, as well as CROs to ensure all applicable analytical test methods are appropriate for the stages of preclinical & clinical development. This is an excellent opportunity to utilize, contribute and advance the ideal candidate’s laboratory skills in a progressive, state-of-the-art and diverse facility. | 05/28/2025 |
| 1170 | NextPhase Mansfield, MA Mechanical Engineer Bachelor's Degree in Mechanical Engineering (B.S., M.E.) Exp: 1-4 years |
The Mechanical Engineer I will collaborate with team members to design and refine cutting-edge medical devices, contributing to product testing, validation, and optimization. Working closely with management, quality assurance, supply chain, and engineering teams, the Mechanical Engineer will oversee all stages of product development, encompassing mechanical design, materials sourcing, prototype fabrication, and the planning and implementation of characterization tests. Responsibilities will also include the development of test protocols, active participation in product testing, and the preparation of comprehensive test reports | 05/28/2025 |
| 1171 | Avecia Milford, MA Research Scientist I, Analytical Development MS Exp: 1+ years |
The Research Scientist I is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. | 05/28/2025 |
| 1172 | Avecia Milford, MA Quality Control Analyst I BS in chemistry, biology or related discipline Exp: 0-2 years |
The QC Analyst I is responsible for conducting routing analysis of raw materials, in-process samples, and finished products in a strict GMP setting. The position involves working in the QC laboratory and in the manufacturing space on assigned tasks following written procedures and verbal instructions. | 05/28/2025 |
| 1173 | NJ Bio Princeton, NJ Scientist, Process Development MS level in Organic Chemistry Exp: 0-2 years |
Under minimal supervision works on multiple steps/multiple projects to execute chemical syntheses from mgs to grams to kilo scales and conduct pilot scale synthesis (kilo scale), purification and characterization of compounds and present results and progress updates to internal and external stakeholders, stay abreast of current literature in scientific areas, maintain equipment, chemical inventory and lab support and Perform duties as required. The incumbent works cross-functionally with internal departments and external resources on process development related issues. The Scientist, Process Development supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 05/28/2025 |
| 1174 | NJ Bio Princeton, NJ Manufacturing Associate I BA/BS degree in a scientific discipline (synthetic /organic chemistry) Exp: 0-2 years |
The Manufacturing Associate I is responsible for the execution of production activities for early phase small molecule and/or biological programs within a GMP environment. The incumbent works cross-functionally with internal departments and external resources on manufacturing related issues. The Manufacturing Associate I supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 05/28/2025 |
| 1175 | NJ Bio Princeton, NJ Assistant Project Manager BS, MS in Chemistry, Biochemistry, Biology, Health Sciences, or other related disciplines Exp: 0-2 years |
We are looking for a dedicated and detail-oriented Assistant Project Manager to join our team. The successful candidate will be responsible for supporting project management activities, ensuring projects are completed on time, within scope, and on budget, while maintaining high levels of customer satisfaction and collaboration. This position requires it to be onsite the vast majority of the time. The incumbent works cross-functionally with internal departments and external resources on project management related issues. The Assistant Project Manager supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 05/28/2025 |
| 1176 | NorthStar Medical Radioisotopes Beloit, WI Radiopharmaceutical Manufacturing Associate (3rd Shift) Bachelor's Degree in a STEM discipline Exp: 1 year |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. Requirements for this position include the ability to work 1st, 2nd, and 3rd shifts during the training period (several months). | 05/28/2025 |
| 1177 | Nova Biomedical Waltham, MA Quality Engineer I BS degree in engineering, the sciences, or another technical discipline. Exp: 1-2 years |
Nova Biomedical is hiring a Quality Engineer I on-site (hybrid) in our Waltham, MA facility. This role will support Quality Assurance activities within the corporate Quality Management System (QMS). Responsibilities include providing expertise and general oversight for the management and improvement of design and development, validations, quality planning, internal auditing, investigations, process controls, change management, quality records, corrective and preventive activities, data management, employee training, and other duties as assigned. | 05/28/2025 |
| 1178 | Nova Biomedical Billerica, MA Quality Engineer I BS degree in engineering, the sciences, or another technical discipline. Exp: 1-2 years |
Nova Biomedical is hiring a Quality Engineer I in our Manning Road, Billerica, MA facility. This role will support Quality Assurance activities within the corporate Quality Management System (QMS). Responsibilities include providing expertise and general oversight for the management and improvement of design and development, validations, quality planning, internal auditing, investigations, process controls, change management, quality records, corrective and preventive activities, data management, employee training, and other duties as assigned. | 05/28/2025 |
| 1179 | Novo Nordisk West Lebanon, NH Quality Control Analyst I - III Raw Materials - Methods Validation Bachelor’s degree in scientific discipline Exp: 1 year |
This position has primary responsibility to support Quality Control operations in the microbiology, analytical or inspection area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This position carries out routine QC testing and may support sampling, investigations, validations, projects and other related support activities for the manufacturing facility and process. This individual works with supervision on routine tasks and detailed instruction on new tasks. | 05/28/2025 |
| 1180 | Novo Nordisk West Lebanon, NH Manufacturing Technician I - IV - BEN Bachelors’ Degree in a science discipline Exp: 0 years |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 05/28/2025 |
| 1181 | Novo Nordisk West Lebanon, NH Quality Control Analyst I - IV Micro Bachelor’s degree in scientific discipline Exp: 1 year |
This position has primary responsibility to support Quality Control operations in the microbiology, analytical or inspection area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This position carries out routine QC testing and may support sampling, investigations, validations, projects and other related support activities for the manufacturing facility and process. This individual works with supervision on routine tasks and detailed instruction on new tasks. | 05/28/2025 |
| 1182 | Novo Nordisk Bloomington, IN Engineer, PM & Tech Transfer Bachelor’s degree in Engineering Exp: 1+ years |
This role will be responsible for the technical transfer of processes from Process Development or our clients. It will also involve drafting and review of documentation, compilation, and assessment of process data, and providing technical input for deviation investigations, change controls, and CAPAs. This role will provide on-call and on-the-floor technical support to manufacturing. This position will be client-facing and should possess the ability to work collaboratively with clients and internal cross-functional stakeholders to move projects forward. | 05/28/2025 |
| 1183 | Novonesis Milwaukee, WI Phage Lab Technician I Bachelor’s degree in microbiology, biology, biotechnology, or a related field Exp: No exp |
As a Phage Lab Technician, you'll gain hands-on experience in a dynamic environment focused on customer support through our phage testing service. | 05/28/2025 |
| 1184 | Novonesis Wausau, WI Quality Control Associate Bachelor’s Degree in Microbiology, Biology, Molecular Biology, Chemistry or related field Exp: 1-3 years |
The Quality Control Team ensures Novonesis delivers high-quality products by maintaining strict adherence to quality, safety, and compliance standards. Their work directly supports the company’s mission of innovation and customer satisfaction. The team fosters a collaborative environment, sharing knowledge and supporting one another in tackling challenges. Together, they conduct inspections, analyze manufacturing data, perform routine testing, and maintain compliance documentation, while also contributing to cross-functional projects aimed at process and product improvement. Looking forward, the team will focus on adopting advanced technologies like automation, predictive analytics, and digital tools to enhance efficiency. They will also play a key role in sustainability initiatives, ensuring compliance with green standards and reducing waste. By combining teamwork, technical expertise, and innovation, the Quality Control Team drives Novonesis’s commitment to excellence and continuous improvement. | 05/28/2025 |
| 1185 | Novonesis Franklinton, NC Recovery Engineer II BS in Chemical Engineering or related field Exp: 1+ year |
Lead recovery optimization in lab and production scale. Provide technical support for troubleshooting efforts and process improvement initiatives. Identify and capture new opportunities for production process improvements. Contribute to closing global gaps on focus products. Ensure projects are aligned with Global Optimization Network guidelines. Lead and motivate project teams towards achieving ambitious yet achievable goals. Support the professional development of peers through scientific guidance. Plan and coordinate experimental work for small and large-scale trials. Conduct experiments and evaluate data to ensure project expectations and deadlines are met. Effectively communicate technical insights and project progress. Recommend improvements in recovery pilot scale equipment and processes | 05/28/2025 |
| 1186 | Novonesis Salem, VA Process Engineer Bachelors degree in an engineering discipline Exp: 1+ years |
In this role you will be responsible for supporting production processes of microbial intermediates and finished goods, as well as supporting capital investment projects. The main aspects of this role include optimization of existing processes and parameters, support and qualification of new product launches at production scale, troubleshooting and structured problem solving for daily process/product support, adhering to and enforcing site safety, environmental, and quality policies, and serving as a technical resource (user manager) for small and mid-sized capital investment projects. | 05/28/2025 |
| 1187 | Nucleus Biologics San Diego, CA Manufacturing Technician I BS/BA in Biology/Immunology Exp: 1+ years |
The Manufacturing Technician I will assist the Manufacturing team and report into the Associate Manufacturing Manager. This individual will sit out of our San Diego, California. | 05/28/2025 |
| 1188 | Nucleus Radiopharma Rochester, MN Quality Assurance Associate Bachelor’s degree in Life Sciences, Quality, or a related field Exp: 0-2 years |
The Quality Assurance (QA) Associate will support the execution and maintenance of our Quality Management System (QMS). This role focuses on quality systems activities including deviation and CAPA coordination, change control tracking, and document control support. They will also assist in the creation of training materials to support GMP and quality compliance initiatives. | 05/28/2025 |
| 1189 | Nurix Therapeutics Woodlands, TX Research Associate I/II, Analytical Development & Quality Control MS Exp: 1+ year |
Nurix Therapeutics seeks a motivated Research Associate to join the Analytical Development and Quality Control group. The Research Associate will operate and maintain lab equipment and instrumentation, conduct sample receipt/analysis/data reporting, and communicate analytical results internally. | 05/28/2025 |
| 1190 | Nurix Therapeutics San Francisco, CA Research Associate I, Pharmaceutical Development (Contactor) BS/BA or higher in chemistry, pharmaceutics, or related field Exp: 1-2 years |
Nurix is looking for a Research Associate, Pharmaceutical Development to provide scientific, technical, and hands-on support of drug discovery and product development related to small molecules from early discovery to clinical trial enabling studies. | 05/28/2025 |
| 1191 | Globus Medical Limerick, PA Associate Quality Engineer Bachelor’s Degree required (science or engineering preferred) Exp: 0-2 years |
The Associate Quality Engineer will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. As a contributor to the quality engineering organization, this professional will be a self-motivated and characterized as an excellent problem solver. This person will play an integral role in maintaining and improving the quality management system, product quality, and manufacturing process quality. | 05/28/2025 |
| 1192 | Globus Medical West Carrollton, OH Industrial Engineer Master's Degree Exp: No exp |
As an Industrial Engineer you will be responsible for driving operational excellence by analyzing workflows, optimizing production processes, and implementing Lean manufacturing principles to enhance safety, efficiency, and productivity. The successful candidate will lead initiatives to develop efficient plant layouts, establish and maintain labor standards, and drive continuous improvement across production operations. In addition to technical expertise, this role requires exceptional problem-solving skills, a proactive mindset, and the ability to influence and collaborate with cross-functional teams. The ideal candidate is a champion of Lean principles, committed to fostering a culture of continuous improvement while delivering measurable results in safety, quality, delivery, and cost. | 05/28/2025 |
| 1193 | Globus Medical Audubon, PA Electrical Engineer MS EE Exp: 1+ years |
We are seeking a highly skilled and motivated Electrical Engineer to join our rapidly growing Digital Health team. You will work closely with a dynamic team of electrical, software, and mechanical engineers to conceptualize and commercialize innovative medical devices to meaningfully impact the lives of patients with musculoskeletal disorders. The ideal candidate will have a strong background designing, building, and testing embedded electrical systems, including firmware design and development. This role requires a balance of creative thinking, analytical design, hands-on prototyping and testing, and systematic product development. | 05/28/2025 |
| 1194 | Ofni Systems Raleigh, NC Computer Systems Validation Engineer BS in math, science or engineering Exp: 1 year |
We are hiring a Validation Engineer to be on the cutting edge of automated validation techniques. You will be responsible for implementing our validation solutions while working with industry-leading companies. Ideal candidates are experts on the requirements of 21 CFR 11, have excellent critical thinking and interpersonal skills, and are motivated to meet client needs for compliance. If you are an A-level engineer who enjoys the challenge of solving real-world compliance problems then we would like to talk with you. | 05/28/2025 |
| 1195 | Olympus Charleston, SC Field Service Engineer I Bachelor’s degree Exp: 1-3 years |
The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 05/28/2025 |
| 1196 | Olympus Charlotte/Asheville/Greensboro, NC Field Service Engineer I Bachelor’s degree Exp: 1-3 years |
The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 05/28/2025 |
| 1197 | Olympus san Jose, CA Repair Engineer I Bachelor's degree in engineering Exp: 1 year |
Provide engineering support for introduction of new products and alternate repair activities. Function as Project Coordinator on more complicated projects as defined by the Manager by providing technical information to other project participants recommending cost effective procedures tracking and maintaining implementation dates and documenting completed projects. Provide support to Associate Engineer on his/her assigned projects. | 05/28/2025 |
| 1198 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology, 1st Shift B.S. degree in Biological or related sciences Exp: 1 year |
This is a 1st shift-based position, working on-site Monday through Friday, from 7am-3:30pm. The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned manufacturing shift supervisor, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 05/28/2025 |
| 1199 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology, 2nd Shift B.S. degree in Biological or related sciences Exp: 1 year |
This is a 2nd shift-based position, working on-site Monday through Friday, from 3pm to 11:30pm. The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned manufacturing shift supervisor, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 05/28/2025 |
| 1200 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology, 3rd Shift B.S. degree in Biological or related sciences Exp: 1 year |
This is a 3rd shift-based position, working on-site Monday through Thursday, from 9pm to 7:30am. The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned manufacturing shift supervisor, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 05/28/2025 |
| 1201 | Orca Bio Sacramento, CA Specialist, Quality Assurance Master’s degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) Exp: 1+ years |
The Specialist, Quality Assurance position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies. | 05/28/2025 |
| 1202 | Organogenesis Canton, MA Production Associate I - Apligraf Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 05/28/2025 |
| 1203 | Organogenesis Smithfield, RI Production Associate Dermagraft Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Dermagraft), under the direct supervision of the Dermagraft Team Leader/Dermagraft Supervisor/Manager. The Dermagraft Associate will support the Dermagraft Manufacturing department by performing the tasks that will assure the safe and timely processing of Dermagraft, working in both a ISO 7 and ISO 8 cleanrooms. | 05/28/2025 |
| 1204 | RoslinCT Hopkinton, MA QC Analyst, Microbiology Bachelor's degree in scientific discipline Exp: 0-7+ years |
The Quality Control Analyst will be responsible for collection of environmental and raw material samples, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. | 05/19/2025 |
| 1205 | RoslinCT Hopkinton, MA Project Engineer Associate Master's degree in engineering/science Exp: 1+ years |
The Project Engineer will execute and provide engineering support for the procurement, enrollment, and installation of equipment and systems. They will also support validation and commissioning activities. This critical role will develop and review related documentation and collaborate with Quality Assurance to ensure adherence to world-wide regulatory requirements and corporate standards. | 05/19/2025 |
| 1206 | RoslinCT Hopkinton, MA Cell Processing Associate Bachelor's degree in biology or related scientific discipline Exp: 0-5 years |
This is a third shift role reporting to the Manufacturing Supervisor. The position's core responsibilities are focused on clinical and commercial manufacturing processes related to cell therapies. Activities include aseptic sampling of products in a Grade A environment, to operate automated, single-use systems for the targeting, expansion, and harvesting. Operate and maintain cell processing equipment. The Cell Processing Associate will support inventory management, suite cleaning, and setup activities per RoslinCT’s governing procedures. This position may require the individual to collaborate as needed with peers within Manufacturing Sciences and Technology (MS&T), Quality, and Facilities. | 05/19/2025 |
| 1207 | Mallinckrodt Greenville, IL Process Engineer B.S in Engineering, Chemical Engineering or related field. Exp: 1-3 years |
The Process Engineer is the recognized technical leader for manufacturing processes and for the improvement of existing processes. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies. Serve as main point of contact for manufacturing processes in their area in regard to safety, quality, and continuous improvement activities. Ensure that the goals and objectives are achieved as they pertain to Safety, Quality, Production, Cost Standards, and Operational Excellence. | 05/19/2025 |
| 1208 | Mallinckrodt Raleigh, NC Quality Analyst II Bachelors or Sciences (BS) or equivalent life science degree Exp: 1-3 years |
The Quality Analyst II has responsibility for Product Release and Maintenance of Monthly Quality Metrics and Daily Notification to Management. They provide support for customer inquiries, gap assessments, batch record review, and label preparation as assigned. | 05/19/2025 |
| 1209 | Masimo Irvine, CA Engineer, Regulatory & Product Safety B.S. or M.S. in Science or Engineering Exp: 0-2 years |
The Engineer, Regulatory and Product Safety is responsible for providing technical support for all aspects of regulatory and product safety throughout the product realization process. This position will handle projects from product inception, development, through manufacture and customer use. The incumbent provides support to ensure product meets defined safety standards and worldwide regulatory requirements. | 05/19/2025 |
| 1210 | Mattek Ashland, MA Production Associate I Bachelor’s Exp: 1 year |
Participates in duties associated with manufacturing of MatTek tissue models according to SOPs where applicable. May also perform duties assigned under Laboratory Assistant, as needed. | 05/19/2025 |
| 1211 | MMT St. George, UT Applications Engineer I Bachelor’s degree in Engineering or a related field. Exp: 1-3 years |
At MMT, our objective is to develop excellence in automation, machine design, material handling, and custom tooling. Each position contributes to the success of the company through accountability, responsiveness, and a solutions-oriented mindset. We are currently seeking an Applications Engineer to join our dynamic catheter and guidewire manufacturing automation site in St. George, UT. The Applications Engineer’s focus will be post-production machine testing and process development, onsite installations, and rapid prototyping and proof of concept for new opportunities. Additional responsibilities include tooling development support for design engineers, customer technical support, and process report writing | 05/19/2025 |
| 1212 | MMT Angleton, TX Technical Sales Engineer I Bachelor’s in Engineering or equivalent Exp: 1-3 years |
At MMT, our objective is to provide world-class solutions for precision hole making applications and contract medical device manufacturing. Each position contributes to the success of the company through accountability, responsiveness, and a solutions-oriented mindset. Working in concert with the appropriate internal and external resources, the Technical Sales Engineer will primarily focus on being a technical expert across all offerings within SYNEO’s Cutting Tools and Specialty Manufacturing Divisions. This position is required to perform Sample Material Evaluations, Inspections, Data Collection, and give feedback for application specific tooling or Specialty Manufacturing processes. The position requires close collaboration with internal manufacturing stakeholders, engineering, and sales resources to develop and implement recommendations that meet or exceed customer expectations. | 05/19/2025 |
| 1213 | MMT Ramsey, NJ Mechanical Engineer Bachelor’s degree in Mechanical Engineering Exp: 1-3 years |
As a Mechanical Engineer at MMT, you’ll be at the forefront of innovation, designing and testing everything from custom machines to robotics. You’ll collaborate with a talented design team, bring your ideas to life using CAD software, and see your work go from concept to production. | 05/19/2025 |
| 1214 | Medtronic Mounds View, MN Quality Engineer I Bachelor's Degree in Engineering, Science or technical field Exp: 0 years |
The Quality Engineer I will have responsibility for ensuring quality within the Global Calibration Services, Midwest Region (GCSMR) department. GCSMR provides calibrations and support for test and measurement equipment used in facilities, research, development, and manufacturing environments in many business environments in the Midwest and throughout global Medtronic. | 05/19/2025 |
| 1215 | Medtronic Swedesboro, NJ Industrial Engineer Bachelor's Degree Exp: 0 years |
Medtronic is hiring in Woolwich County, here our employees are helping us deliver on the extraordinary. We actively seek a diverse workforce at every level: We require fresh ideas and inclusive insights to maintain our position as an innovative industry leader. That’s why we actively seek, attract, and develop employees who are patient-centric, passionate, and who reflect the wide variety of life experiences found among our patients. | 05/19/2025 |
| 1216 | Medtronic Danvers, MA Quality Engineer II, Manufacturing Operations Master's Degree in engineering/science Exp: 0 years |
We are seeking a Quality Engineer II who is passionate about ensuring product quality and regulatory compliance in support of innovative medical devices. In this role, you’ll contribute to cross-functional efforts and continuous improvement in a dynamic, collaborative environment. In this role you will have responsibility for providing comprehensive manufacturing quality support for commercial medical devices in the area of component manufacturing. This includes activities related to test method validation, process validation, inspection improvements, and process/quality change initiatives. | 05/19/2025 |
| 1217 | Medtronic Tempe, AZ Quality Systems Specialist Master's Degree in engineering/science Exp: 0 years |
In this exciting role as a Quality Systems Specialist – CAPA Specialist supporting the Tempe Campus - you will have responsibility for compliance to the Corrective and Preventive Action (CAPA) processes and Medical Device regulations and requirements, serve as a CAPA subject matter expert; provide guidance to CAPA owners and CAPA Board members to develop CAPA activities and conduct assessment of CAPA documentation. The Quality System CAPA Specialist will ensure compliance with Medtronic policies, FDA regulations, ISO 13485, and other requirements by rigorously assessing CAPA activities and documentation. They will participate in CAPA Board activities, provide guidance and mentorship on CAPA processes and tools, and report on CAPA metrics. Additionally, they will support the development and implementation of CAPA procedures, software, and training, and assist in internal and external audits and inspections. | 05/19/2025 |
| 1218 | Medtronic Mounds View, MN Reliability Engineer I - Cardiac Rhythm Management Bachelor’s degree in Engineering or related field Exp: 0 years |
This Engineer will have the opportunity to support the entire CRM product portfolio through authoring, submission, and maintenance of Periodic Safety Update Reports (PSUR) and other risk management deliverables. This position regularly collaborates with Clinical Evaluation and Regulatory to complete post market surveillance deliverables. This role provides and evaluates the data necessary to support the corrective action (CAPA) and other internal processes (regulatory, clinical, R&D, etc.). This may include support requests for information related to product performance from competent authorities, Medtronic geographies, customers and management. Supports Reliability Engineering with data collection and analysis and regularly communicates product performance data to the organization (via email, product performance meetings and management reviews), or other requests from management. | 05/19/2025 |
| 1219 | Medtronic Minneapolis, MN System Test Engineer II -Neuro Master's degree in Engineering Exp: 0 years |
This position will lead all testing efforts for the Translational Research System team on Neuromodulation & Pelvic Health Implantable products such as cutting-edge neurostimulator systems for Deep Brain Stimulation, Spinal Cord Stimulation, and Sacral Nerve Modulation. The individual will support all test-related phases of development including definition, design, troubleshooting, characterization, and verification of medical device research systems. The individual will be an integral part of the R&T organization delivering the highest quality, life changing technology to our patients. This role requires a strong background in testing, problem solving, and issue investigation with a passion for improving healthcare through technology. | 05/19/2025 |
| 1220 | Medtronic Northridge, CA Quality Engineer II Master's degree in Engineering, Science or technical field Exp: 0+ years |
At Medtronic Diabetes, we are looking for a Quality Engineer II who will have responsibility for providing technical and quality systems expertise within the Operations Quality organization. You will serve as a subject matter expert by providing support for Diabetes commercialized products and projects. Our quality team is looking for talented career engineers to join our organization. We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations. This role will be part of Electronic Technologies and China Operations Quality team. Individuals in this role will provide technical support and quality system expertise for commercialized Diabetes products including Continuous Glucose Monitoring Systems (CGMS) and product accessories. The ideal candidate for this position has a strong technical background and experience in medical device product manufacturing. | 05/19/2025 |
| 1221 | Merck West Point, PA Scientist, Translational Medicine (Hybrid) Master’s degree in Life Sciences Exp: 1+ years |
Translational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration with Discovery Sciences and late-stage Clinical Research across all therapeutic areas. Our team is focused on innovation and dedicated to translating breakthrough science into innovative medicines that extend and improve the lives of patients worldwide. Through clinical trials, we ensure the safety and efficacy of our pipeline and existing products to produce safe, effective, innovative medicine. | 05/19/2025 |
| 1222 | Meridian Bioscience Memphis, TN Quality Assurance Associate Bachelor’s degree in life science, chemistry, pharmaceutical science, statistics, or health/human services related field Exp: 0-5 years |
The Quality Assurance (QA) Associate will support QA processes, programs, and conduct QA activities. This position will uphold standards, methods, and procedures for all stages of production. This position will identify continuous process improvement areas, in compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GLP) processes and documentation for quality control activities. This requires excellent technical skills and abilities, analytical and mathematical skills, organizational and time-management skills, verbal, and written communication skills, plus ability to apply attention to detail. | 05/19/2025 |
| 1223 | Meridian Bioscience Cincinnati, OH Senior Research Associate Master of Science degree Exp: 1 year |
Primary role is to run experiments, acquire and record data, analyze data, draw conclusions for discussion and recommend decisions. | 05/19/2025 |
| 1224 | Mikart Atlanta, GA Quality Control Analyst Chemist Bachelor of Science in Chemistry or in a related science Exp: 0-1 years |
The Quality Control Analyst Chemist for Mikart, LLC is responsible for conducting analyses on various components, in-process materials and finished dosage forms. | 05/19/2025 |
| 1225 | MIMEDX Marietta, GA Associate Product Development Engineer BS/BA in relevant discipline Exp: 0-2 years |
The Associate PD Engineer I will support the operation of the PD group. Candidate will participate in new product development and sustaining engineering activities by following pre-defined protocols and test methods. Some data interpretation will be required. Delegated tasks and procedures are expected to be completed in a thorough and timely manner and communicated to senior PD staff. | 05/19/2025 |
| 1226 | Minaris Allendale, NJ QA Associate II BS degree in a scientifically related field Exp: 1-3 years |
The Quality Assurance Associate plays a pivotal role in ensuring that all quality assurance activities are conducted efficiently and accurately. Under direct supervision, the associate supports daily tasks that are essential for maintaining and improving quality systems and adhering to client-specific procedures. Key responsibilities include document management, review of manufacturing batch records, quality control (QC) data, facilitating material releases, overseeing final product releases, and providing essential assistance to the Quality Management as needed. | 05/19/2025 |
| 1227 | Merck St. Louis, MO Quality Control Associate Scientist Bachelor’s degree in Chemistry, Biochemistry, Biology, or other Life Science discipline Exp: 1+ years |
The Associate Scientist role performs lab testing and supports tasks to assure our product quality meets specifications. | 05/19/2025 |
| 1228 | Merck Sheboygan Falls, WI Associate Quality Control Chemist (Laboratory) Bachelor's Degree in Chemistry, Biochemistry or other Life Science discipline Exp: 1+ years |
The Associate Quality Control Chemist at MilliporeSigma will evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. The QC Chemist is also responsible for the general maintenance and upkeep of the analytical instruments that reside in the QC labs, and assists with managing existing service contracts and the onboarding and retirement of instruments. | 05/19/2025 |
| 1229 | Merck St. Louis, MO Operations Integration Scientist Bachelor's Degree in Chemistry, Biochemistry or other Life Science discipline Exp: 1+ years |
The Operations Integration Scientist is the leading role for the integration and implementation of new custom manufacturing products into the GMP manufacturing facilities. This technically sound position works cross-functionally at multiple manufacturing facilities with Project Management, Quality, Manufacturing, Process and Analytical Development, and customer to efficiently bring new custom/contract manufacturing bioconjugation products into the GMP manufacturing facilities. You manage the technology transfer into GMP by authoring technical documents such as specifications and risk assessments, driving Change Control for new and existing custom manufacturing projects and planning for operational requirements. We’re looking for a candidate with strong technical skills, demonstrated ability to work within a cross- functional team, and excellent interpersonal and team building skills. The position will be based in St. Louis, Missouri. | 05/19/2025 |
| 1230 | Merck St. Louis, MO Associate Production Scientist Bachelor’s degree in Biochemistry, Biology or other Scientific discipline. Exp: 1+ years |
The Associate Production Scientist role is focused on creating manufactured kits of reagents to support Multiplex, ELISA, and RIA kits in the Immunoassay Platform Solutions (IPS) portfolio in a timely manner. | 05/19/2025 |
| 1231 | Merck St. Louis, MO Associate Scientist - Manufacturing Histology Bachelor's degree in Chemistry, Biochemistry, Biology, or other Life Science discipline Exp: 1+ years |
Under moderate supervision, the Associate Scientist – Mfg Histology performs slide manufacturing, H&E staining, IHC staining, and other laboratory operations in Manufacturing associated with slide manufacturing and block qualification according to standard operating procedures (SOPs) and regulatory requirements; assists with document updates as necessary. | 05/19/2025 |
| 1232 | Merck St. Louis, MO Manufacturing Compliance Specialist Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other Life Sciences or Engineering discipline Exp: 1+ years |
MilliporeSigma in St. Louis, MO is seeking a Manufacturing Compliance Specialist for the Ewing Facility in St. Louis, MO. This Compliance Specialist will be responsible for supporting the Ewing operations through the management of quality records (deviations and CAPAs), managing the creation and updates of operating procedures, and assisting label issuance/management for production. This role will work collaboratively with QA, QC, Operations, Engineering, Validation, Process Development and Maintenance while adhering to GMP principles. | 05/19/2025 |
| 1233 | Merck St. Louis, MO Quality Assurance Product Release Specialist Bachelor’s Degree in a scientific (Biology, Chemistry, etc.) or engineering discipline (Chemical, Mechanical, etc.) Exp: 1+ year |
The Quality Assurance Product Release Specialist plays a critical role in ensuring the timely and compliant release of purchased and produced goods at MilliporeSigma. This position is responsible for performing a variety of quality review functions according to established criteria and guaranteeing that products meet all necessary specifications and regulatory requirements. The Quality Product Release Specialist will collaborate with various internal stakeholders and will be a subject matter expert in QA product release processes. | 05/19/2025 |
| 1234 | Modulo Bio San Diego, CA Stem Cell Scientist MS in Genetics, Molecular Biology, Developmental Biology, Biochemistry, Regenerative Medicine, Neuroscience, or related field Exp: 1+ years |
Modulo Bio is seeking a Stem Cell Scientist to develop and scale an induced-pluripotent stem cell (iPSC)-based in vitro model of the neuroimmune system. Modulo Bio is building a proprietary immune cell modeling platform, which incorporates human genetics, functional genomics, molecular biology, cellular and tissue profiling, disease model engineering, and advanced computational models. The successful candidate will build a complex cell model platform with the goal of improving our understanding of human biology and therapeutic interventions to inform early and late stage pipeline efforts. Candidates with an eagerness to work within a highly leveraged, team-driven, dynamic research environment will be prioritized. The candidate will work in close collaboration with our internal Computational Biology group which is focused on next-generation sequencing (NGS), functional genomics, cell or tissue profiling, and bioinformatics analyses of cutting-edge large-scale genetic screening or single-cell technologies to enhance our analytic capabilities and to reveal the underlying mechanisms of human disease. | 05/19/2025 |
| 1235 | Moog Murphy, NC Manufacturing Engineer Bachelor's degree in Engineering/Engineering Technology or equivalent Exp: 1 year |
Our team in Moog Industrial Group is looking for a Manufacturing Engineer to join them. You will report to the Site Manager and will have an onsite work schedule in Murphy, North Carolina. | 05/19/2025 |
| 1236 | Novartis Durham, NC Bioprocess Engineer I Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field Exp: 1-2 years |
The Bioprocess Engineer I is responsible for executing assigned manufacturing tasks and activities according to the production schedule to ensure timely production of products that meet quality standards in compliance with relevant GMP, safety, and environmental guidelines. The role level will be determined by the years of relevant experience. The role is located on-site in our Durham, NC location. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. | 05/19/2025 |
| 1237 | Novartis Millburn, NJ Production Technician I Bachelor’s degree in relevant Engineering or Scientific discipline is highly preferred Exp: 1+ years |
Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. | 05/19/2025 |
| 1238 | Novartis Indianapolis, IN Production Technician I Bachelor’s degree in relevant Engineering or Scientific discipline is highly preferred Exp: 1+ years |
Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. | 05/19/2025 |
| 1239 | Novartis Indianapolis, IN QC Technician Bachelor’s degree in microbiology, chemistry or a related field Exp: 1 year |
We are seeking a highly motivated and detail-oriented Quality Control (QC) Technician to support both Microbiology and Chemistry functions at our We are seeking a highly motivated and detail-oriented Quality Control (QC) Technician to support both Microbiology and Chemistry functions at our radioisotope production site. The primary responsibility of this role will be to perform routine quality control testing and analytical functions to ensure the production of high-quality radioisotopes. The QC Technician will work closely with the Quality Control and Production teams to maintain regulatory compliance, meet GMP (Good Manufacturing Practices) standards, and ensure the safety and efficacy of products produced at our Indianapolis Isotopes facility. | 05/19/2025 |
| 1240 | Novartis Morris Plains, NJ Manufacturing Operations Specialist Bachelor’s degree Exp: 1 year |
The Manufacturing Operations Specialist is responsible for the dispensary / ISO8 area tasks including kitting and material flow, inventory management and other duties required to support the core functions. | 05/19/2025 |
| 1241 | Natera San Carlos, CA Clinical Lab Associate BS/BA in a biological science or similar field of study Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. | 05/19/2025 |
| 1242 | Natera Austin, TX Clinical Lab Operator Horizon BS/BA in a biological science or similar field of study Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. | 05/19/2025 |
| 1243 | Natera Austin, TX Clinical Lab Operator I BS/BA in a biological science or similar field of study Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. | 05/19/2025 |
| 1244 | KARL STORZ Goleta, CA Design Verification Test Engineer II MS degree in Electronics Technology/Engineering or related field Exp: 0-3 years |
We're looking for a talented Design Verification Engineer to join our team! As a key player in ensuring our products meet the highest quality standards, you'll design and execute verification procedures, troubleshoot issues, and train other test engineers. If you're passionate about delivering exceptional results and collaborating with top-notch professionals, we want to hear from you! | 05/12/2025 |
| 1245 | KBI Biopharma Durham, NC Manufacturing Specialist I Master’s degree in a related scientific or engineering discipline Exp: 0+ years |
Responsible for leading technical support activities for GMP Manufacturing Operations in a multi-product, large scale biopharmaceutical facility. This role will support, but not limited to the following: Drafting, routing, and revision of manufacturing batch records, support records, and standard procedures. First line of defense for manufacturing events. Individual will assess, provide, and help implement immediate corrective and preventative actions. Provide manufacturing process support during on-going shop floor execution as needed. Support new equipment enrollment workflow from purchasing to qualification as needed. SME support on critical laboratory equipment supporting manufacturing operations. Additionally, SME will lead and manage all activities and event related to critical laboratory equipment. Support safety initiatives, compliance, and quality requirements. | 05/12/2025 |
| 1246 | KBI Biopharma Durham, NC Manufacturing Associate I (Night Shift) Bachelor’s degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II is responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II must follow the instructions depicted in SR’s, EPR’s, BR’s, SOP’s and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including ‘Right the First Time’ (RFT). The candidate will maintain a sense of ownership of the production processes, manufacturing environment and facility. They will be exposed to various unit operations including media/buffer preparation, shake flask operations, seed expansion, bioreactor setup and operations, cell culture harvest setup and operations, aseptic technique, chromatography, ultrafiltration, and drug substance filling operations; as well as to analytical tools and general biotechnology auxiliary equipment (pumps, sterile tubing welders and sealers, pH/Conductivity/osmolality meters). Following task execution, the Manufacturing Associate I/II will review the executed production records (SR’s, ERP, and BR’s) to ensure GxP compliance. | 05/12/2025 |
| 1247 | KBI Biopharma Durham, NC Validation Engineer I Bachelor’s degree in Chemical Engineering, Industrial Engineering, Biomolecular Engineering, Mechanical Engineering, or related scientific field. Exp: 1-3 years |
The Validation Engineer I/II will be responsible for facilitating the validation lifecycle process for the Validation Department to ensure all equipment and systems are in a qualified state suitable for the intended use. This may entail, assisting with the planning, development, project management, and execution of life cycle engineering and validation lifecycle documentation elements of engineering and validation lifecycle design, commissioning, maintenance, qualification, and the interfaces with quality system lifecycle compliance requirements. This position will provide support for more than one area of subject matter expertise for validation disciplines which may include: Facilities qualification, Utilities qualification, Equipment qualification, Manufacturing process control system qualification and Cleaning validation. | 05/12/2025 |
| 1248 | KBI Biopharma Boulder, CO Manufacturing Associate I (Night Shift) Bachelor’s degree Exp: 0-5 years |
Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels. | 05/12/2025 |
| 1249 | KBI Biopharma Durham, NC Manufacturing Specialist I Master’s degree in a related scientific or engineering discipline Exp: 0+ years |
Responsible for leading technical support activities for GMP Manufacturing Operations in a multi-product, large scale biopharmaceutical facility. This role will support, but not limited to the following: Drafting, routing, and revision of manufacturing batch records, support records, and standard procedures. First line of defense for manufacturing events. Individual will assess, provide, and help implement immediate corrective and preventative actions. Provide manufacturing process support during on-going shop floor execution as needed. Support new equipment enrollment workflow from purchasing to qualification as needed. SME support on critical laboratory equipment supporting manufacturing operations. Additionally, SME will lead and manage all activities and event related to critical laboratory equipment. Support safety initiatives, compliance, and quality requirements. | 05/12/2025 |
| 1250 | KBI Biopharma Louisville, CO Research Associate I Bachelor’s degree in a scientific discipline Exp: 0-2 years |
Join an analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Characterization Services team. The individual in this position will support product characterization studies of biopharmaceutical products through executing experimental protocols, performing data analysis, documenting work in technical reports, and presenting results to clients and management. Bioanalytical testing may include (but not limited to) HPLC, electrophoresis, mass spectrometry, and biophysical techniques. Required to work in teams to solve scientific problems, and to train and be trained by colleagues. | 05/12/2025 |
| 1251 | KBI Biopharma Durham, NC Research Associate I Bachelor’s or Master's degree in chemistry, biochemistry or related area (or equivalent training) Exp: 0+ years |
Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical and Formulation Sciences (AFS) Department. The individual in this position will be responsible for executing experimental protocols and performing data analysis in biopharmaceutical laboratories. | 05/12/2025 |
| 1252 | Kindeva Union City, CA Analytical Scientist BS in Chemistry or in a pharmaceutical related discipline. Exp: 1+ years |
Analytical Scientist required to support multiple R&D activities in Union City. This is a key role within an expanding team of formulation and product development scientists and offers the successful candidate an opportunity to make a significant contribution to the development of new inhalation products and future technologies by applying their creative technical skills and using their scientific experience. We develop drugs including proteins peptides, other biologic compounds as well as small molecules. | 05/12/2025 |
| 1253 | Kindeva Lexington, KY QC Microbiologist - Third Shift BA/BS degree in Chemistry, Biology, Microbiology, or related field Exp: Entry Level |
As a Microbiologist I, you will play an essential role in protecting product quality and ensuring a contamination-free environment. Your daily work will directly support the safety and reliability of our pharmaceutical products through environmental monitoring and microbiological testing. By mastering aseptic techniques and partnering closely with experienced professionals, you will help maintain high laboratory standards, ensure regulatory compliance, and build a strong foundation in microbiological quality control. Your attention to detail and commitment to excellence will contribute to patient safety and support our mission to deliver life-changing therapies with integrity and care. | 05/12/2025 |
| 1254 | Kindeva Bridgeton, MO Quality Engineer Master's degree in a scientific or engineering discipline Exp: 1-3 years |
In this role, you will develop, direct, and lead Quality oversight for process improvements in equipment and material preparation, aseptic compounding, filling, inspection, and packaging at the Brentwood, Maryland Heights, and Bridgeton facilities. You will coordinate support activities, reviews, audits, and the release of semi-finished products and components to align with site-wide objectives. You will collaborate with cross-functional teams to support continuous improvement initiatives, incident investigations, and change management. Additionally, you will make decisions related to Incident Investigations and Corrective and Preventive Actions, ensuring a focus on overall quality, site priorities, and operational success. | 05/12/2025 |
| 1255 | Kite Santa Monica, CA Sr. Research Associate - Viral Vector Upstream MS/MA in Chemical/Biochemical Engineering, Biochemistry, Biology or related field Exp: 0+ years |
Kite Pharma is seeking a creative and highly motivated Sr. Research Associate to join our growing vector process design team in Santa Monica. In this integral role, you will contribute to the company's pipeline development for hematopoietic and solid tumor malignancies by supporting the development, scale-up, process characterization, and technology transfer of the lentiviral vector process. | 05/12/2025 |
| 1256 | Krystal Moon Township, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 05/12/2025 |
| 1257 | Krystal Pittsburgh, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 05/12/2025 |
| 1258 | Krystal Pittsburgh, PA Research Associate, Analytical Sciences and Clinical Testing Services Bachelor’s degree (Biology, Biochemistry, Chemistry, or related science) Exp: 0-3+ years |
Krystal Biotech, Inc is seeking a highly motivated Research Associate, Analytical Sciences and Clinical Testing Services to perform high quality analytical testing in support of Krystal’s process development, product development, and clinical sample analysis efforts. This position will be laboratory based, Monday-Friday standard hours. | 05/12/2025 |
| 1259 | Krystal Pittsburgh, PA Clinical Trial Associate/Clinical Research Coordinator BS/BA degree required in science/health-related field. Exp: 1-3 years |
Krystal Biotech, Inc. is seeking a Clinical Trial Associate to support our Clinical Operations Team. The Associate's responsibilities will entail, but not be limited to, assisting with the management and inventory of clinical supplies, ensuring proper materials are available at clinical sites in a timely manner, and working with the Clinical Operations team to support multiple Clinical Trials. Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. | 05/12/2025 |
| 1260 | Krystal Pittsburgh, PA Process Validation Associate Bachelors’ Degree in Chemical Engineering, Biomedical Engineering, or related Exp: 1+ year |
Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) or Engineer (3+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site. | 05/12/2025 |
| 1261 | Kyowa Kirin Sanford, NC Project Automation Engineer Bachelor’s degree in Engineering Exp: 1 year |
A project automation engineer to assist in design and start-up of a new manufacturing facility. The project automation engineer will work directly with the Site Head during the project phases and then transition to an operational role in the plant. The Automation Engineer is responsible for the design, commissioning, and operation of key KKNA Manufacturing Facility automated systems. | 05/12/2025 |
| 1262 | LabConnect Cleveland, OH Clinical Sample Specialist Bachelor’s degree Exp: 6 months |
The Clinical Sample Specialist is responsible for biospecimen management activities for samples arriving at the LabConnect Cleveland facility. The Specialist will perform tasks in support of receiving specimens for storage, onsite processing, distribution to biorepository, and shipments to partner laboratories or other facilities. Additional activities include maintenance of specimen storage equipment, monitoring accessioning and biorepository consumables, and the organization of departmental SharePoint documentation. The Specialist will regularly communicate across departments and interact with project management, facilities, data management, and IT. | 05/12/2025 |
| 1263 | LG Chem Evansville, IN Associate Chemist Bachelor’s Degree in Chemistry or Related Scientific Field Exp: 1+ years |
The Associate Chemist is responsible for analytical, environmental and physical testing He or she also performs testing on raw materials and compounded products. This person will also participate in the development and formulation of new products under the direction of a Chemist or Senior Chemist. The Associate Chemist may provide any necessary technical support to various other departments. In addition, he or she is responsible for any other task the Chief Technology Officer deems necessary. | 05/12/2025 |
| 1264 | LGC Clinical Diagnostics Cumberland Foreside, ME Manufacturing Chemist I Bachelors degree in life science field or other related science or medical curriculum Exp: No exp |
The Manufacturing Chemist I fulfills the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 05/12/2025 |
| 1265 | LGM Pharma Rosenberg, TX Quality Assurance Specialist Bachelor’s degree in a scientific discipline Exp: 1+ years |
Performs initial, in-process and final inspections during manufacturing/packaging of product; resolves inspection findings with Packaging Manager and /or QA Manager. Collects product samples for product release testing, process validation testing and product stability as applicable and prepare labels at completion of packaging. Prepares documentation and forward samples to QC Lab for required testing; records information on batches in-process of testing on QC board; notifying QC of any urgent testing. Monitors incoming materials as received in Quarantine. Reviews material received paperwork and compare to material received for accuracy; notifying Materials Department to call supplier if CofA has not been received or CofA is incomplete. Coordinates with production areas to anticipate material usage to meet required schedule. Performs other related duties as required. | 05/12/2025 |
| 1266 | Liquidia Morrisville, NC Quality Control Associate Scientist B.S. degree in chemistry, pharmaceutical sciences, or a similar scientific field Exp: 0-2 years |
We are looking for an Associate Scientist, Quality Control. In this “hands-on” role within the Quality Control Lab, the Associate Scientist will join a talented and collaborative team that welcomes input and suggestions to help continue Liquidia’s upward trajectory at the most exciting time in the Company’s history. Critical to success are a scientific laboratory background, ability to follow CGMP documentation requirements, and excellent communication skills. The Associate Scientist will conduct laboratory analysis of raw materials and intermediates in support of Liquidia’s lead product candidate. | 05/12/2025 |
| 1267 | Liquidia Morrisville, NC Manufacturing Technician B.S. degree in chemistry, pharmaceutical sciences, or a similar scientific field Exp: 0-2 years |
We are looking for a hands-on and experienced Manufacturing Technician. In this role, you will perform routine running of manufacturing equipment to support production and R&D efforts. Furthermore, you will provide feedback to engineering and scientific staff on process performance and ideas for process improvement. | 05/12/2025 |
| 1268 | Lonza Portsmouth, NH Manufacturing Associate I (Nights) BS in a Science related field Exp: 0-4 years |
Join Lonza as a Manufacturing Associate Level I for a remarkable chance to contribute to producing therapeutic proteins in New Hampshire, USA. Work with a top team to implement innovative ideas for improving lives under cGMP conditions! Working nights from 7pm-7am on a rotational schedule. | 05/12/2025 |
| 1269 | Lonza Houston, TX QC Investigator II Bachelor’s degree in a scientific subject area or related field. Exp: 0-4 years |
At Lonza AG, we are driven by the ambition to deliver best-in-class healthcare solutions. Our QC Investigator II role is an outstanding opportunity to join a team that flourishes with innovation and quality. This position is based in Houston, TX, and is vital to our mission of achieving detailed results by closely adhering to quality standards. Your confirmed ability to efficiently implement corrective actions and lead continuous improvement initiatives will be the cornerstone of your success with us! | 05/12/2025 |
| 1270 | Lonza Greenwood, SC Lab Technician Bachelor’s degree or equivalent experience in a scientific field (e.g., Biology, Chemistry, Food Science, Nutrition, or related subject area) Exp: 1+ years |
Become an essential part of a world-class team at Lonza AG as a Lab Technician in Greenwood, SC, USA! This outstanding opportunity allows you to support critical R&D functions, formulation development, and testing. Join us in our ambitious mission to improve lives through science. | 05/12/2025 |
| 1271 | Lotte Biologics Syracuse, NY Associate Scientist, Upstream Process Development M.Sc./M.Eng degree Exp: 0-2 years |
The primary role of the Associate Scientist, Upstream Process Development is to execute laboratory experiments in the development, optimization, characterization, and scale-up of biologics upstream cell culture processes from laboratory to manufacturing scale using knowledge of cell culture, cell banking, medium preparation, bioreactor production, and primary recovery. The role is a combination of laboratory- and office-based work. This role will execute and document laboratory studies in laboratory notebooks. Additionally, this role will support documentation review, protocols, technical reports, change controls, and CMC regulatory submissions under supervision. The Associate Scientist is expected to follow detailed GLP/GMP procedures and safety requirements. This role will work in a team environment and will interact with other functional departments. Additionally, this position is a team-based position that may require work on evenings, weekends, and holidays | 05/12/2025 |
| 1272 | Lotte Biologics Syracuse, NY Assistant Scientist, Quality Control BS degree in scientific area Exp: 0-3 years |
The role of Assistant Scientist within our Quality Control Release department conducts routine general chemical and/or biological testing of materials and products for in-process, release and stability purposes, in compliance with all applicable procedures and regulations. A variety of duties are performed relating to the efficient and effective functioning of the Quality Control lab. | 05/12/2025 |
| 1273 | Lilly Pleasant Prairie, WI Process Engineer Bachelors Degree in Engineering Exp: 1+ years |
Engineer - Process is responsible for establishing and maintaining the reliable operation and qualified state of the equipment and business processes in the area that they support. Ensure that equipment is in-control, compliant, and capable of meeting customer needs, while also driving associated continuous improvement effort. | 05/12/2025 |
| 1274 | Lilly Lebanon, IN Process Engineer - Lilly Medicine Foundry BS or MS in chemical engineering or related discipline Exp: 1-4 years |
We are seeking a Process Engineer to support the pilot plant facility in Lebanon with a focus on peptide and oligonucleotide synthesis. This position involves solving technical challenges with equipment design, developing and sustaining process knowledge, optimizing processes, and managing equipment capabilities. | 05/12/2025 |
| 1275 | Lilly Lebanon, IN Automation Engineer, Drug Substance - Design & Delivery, Lilly Medicine Foundry Bachelor of Science Degree in engineering or a related science field Exp: 1 year |
The Engineer – Automation - Drug Substance Design / Delivery role requires a 4-year engineering degree, preferably in Chemical, Mechanical, Electrical Engineering, or related science field. The position requires high learning agility and a background in DCS programming (preferably DeltaV) and experience in automated API manufacturing or related processes. This role will initially be in support of the design and delivery phase of the project, as part of the Global Process Automation & Control Engineering (GPACE) team. As the site nears completion and start-up activities begin, this role will transition into a Lebanon Site role for long term operational support. GPACE is part of Lilly’s Corporate Engineering Tech Center (ETC). GPACE provides automation, measurement, and process control solutions, and is a technical resource for training, standards, capital project delivery, and Lilly’s standard automation platforms. GPACE’s primary customers are global manufacturing and development sites, Manufacturing Information Technology, and peer groups such as Global Facilities Delivery (GFD). | 05/12/2025 |
| 1276 | Lilly Lebanon, IN Manufacturing Associate - Advanced Manufacturing Bachelor''s degree in STEM field Exp: 1+ years |
The Manufacturing Associate will be responsible for performing routine manufacturing activities across GMP manufacturing areas, including: Cell Culture, Downstream Purification, and Fill & Finish at the Lebanon Advanced Therapies, LP2 site. Initially, the Manufacturing Associate will be responsible for supporting execution of equipment qualification, developing site operations procedures and setting up production areas. During this initial project delivery/startup phase of the project, roles will be fluid and dynamic. Once the plant is operational, the Manufacturing Associate will be responsible for execution of production activities on their shift under the leadership of the shift supervisor. | 05/12/2025 |
| 1277 | Lilly Lebanon, IN Sterility Assurance Scientist - Advanced Therapies Manufacturing Bachelors in Microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline Exp: 1+ years |
Sterility Assurance – Technical Services/Manufacturing Scientist (TS/MS) role is a technical position that develops and implements the site’s sterility assurance related initiatives and provides technical leadership with regard to sterility assurance & environmental monitoring strategies. Primary objectives include the start-up and compliant manufacturing of gene therapy drug product and drug substance, particularly as it relates to development and implementation of sterility assurance strategies, including environmental monitoring, aseptic process simulations, facility cleaning, facility sanitization, and sterility assurance risk management. | 05/12/2025 |
| 1278 | Lilly Indianapolis, IN Scientist – API Manufacturing Process Support Master's Degree in STEM Discipline Exp: 1 year |
The Manufacturing Scientist provides the technical support required to achieve the reliable and compliant manufacture of the Active Pharmaceutical Ingredient External Manufacturing (API EM) portfolio which includes raw materials, intermediates, enzymes and bulk drug substances. The API EM Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and technically independent in setting up and executing a variety of experiments at the laboratory scale and conduct research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 05/12/2025 |
| 1279 | Lilly Indianapolis, IN Chemist - Oligonucleotide Chemistry Bachelors and/or Masters in Chemistry or related scientific field Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for a collaborative, creative and energetic problem solver to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to accelerate the core capabilities and development of internal RNAi-based clinical candidates. | 05/12/2025 |
| 1280 | Lumen Bioscience Seattle, WA Manufacturing Compliance Associate Bachelor's degree in a relevant scientific discipline Exp: 1-2 years |
Lumen Bioscience is seeking a detail-oriented Manufacturing Compliance Associate to support our GMP operations and ensure compliance within our pharmaceutical manufacturing environment. This role involves conducting thorough investigations of manufacturing deviations, identifying root causes, and implementing effective corrective and preventive actions. If you have a passion for quality, strong technical writing skills, and enjoy collaborating across teams, we encourage you to apply. | 05/12/2025 |
| 1281 | Lumos Remote, Quality and Compliance Specialiss Bachelor's Degree ( four year college or technical school) Required, Field of Study: Biology, Chemistry, or related technical discipline Exp: 1-3 years |
Join us in our pursuit to make a difference. Together, we can change the future of medicine! This position reports to the Vice President, Quality and Compliance and is responsible for providing quality support of product development and clinical trial activities and associated functions performed by external contract research, development and manufacturing organizations. This position also supports internal quality systems and compliance functions. The Quality and Compliance Specialist is expected to execute established processes involving quality assurance, quality systems and compliance. | 05/12/2025 |
| 1282 | RoslinCT Hopkinton, MA QC Analyst II, Microbiology 3rd Shift Bachelor's Degree in scientific discipline, Microbiology focus Exp: 0-7+ years |
The Quality Control Microbiology, QC Analyst will be responsible for collecting environmental samples in clean room areas to support manufacturing operations, sample management activities, and testing of cell therapy in-process and release product samples. The person will be responsible for reporting data and writing/revising standard operating procedures (SOPs) and test methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Microbiology will partner with the QC analytical team, interface with multiple groups including manufacturing, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 05/12/2025 |
| 1283 | RoslinCT Hopkinton, MA QC Analyst I/II, Analytical 3rd shift Bachelor's Degree in scientific discipline, Microbiology focus Exp: 0-5+ years |
The Quality Control Analytical, QC Analyst will be executing analytical methods such as appearance, pH, osmolality, cell counting, ELISAs, flow cytometry and related methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Analytical will partner with the analytical team, interface with multiple groups, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. He/she will be responsible for authoring Standard Operating Procedures (SOPs), specifications and Test Methods. He/she will assist in the implementation of new assay methodologies and the associated instrumentation. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 05/12/2025 |
| 1284 | Illumina San Diego, CA Packaging Engineer Bachelor’s degree Exp: 0-2 years |
Develops new packaging or containers to meet established requirements and maintains oversight and quality of existing packages/containers for all product groups. Defines package requirements for product groups and customer requirements. Develops recommendations according to the nature of the product, cost limitations, legal requirements, and the type of protection required, taking into consideration the need for resistance to external variables. May be responsible for coordination of activities and logistics at secondary contract packaging and labeling sites. Responsibilities may include documentation management and an understanding of good manufacturing practices (GMPs). Uses appropriate tools and performs integrity analysis of packaging and improves manufacturing techniques. | 05/04/2025 |
| 1285 | Illumina San Diego, CA Facilities Engineer 1 Bachelor’s or Master's Degree in Engineering, Mechanical Engineering, Electrical Engineering Exp: 0-2 years |
The Facilities Engineer 1 will be responsible for developing and executing validation protocols as related to new or upgraded facilities and utilities as used for medical device manufacturing. This person will work cross-functionally to assist with the development of requirements based on their expertise in clean rooms, water systems, HVAC and other systems used to support a regulated manufacturing environment. This person will also be responsible for report writing. | 05/04/2025 |
| 1286 | Illumina San Diego, CA Scientist 1 Bachelor’s degree Exp: 0-2 years |
We are looking for an enthusiastic and motivated individual for this Scientist 1 position within the Core Services Library Prep Lab to help run day to day operations. Our ideal candidate will work cross functionally with the team and other groups sharing and using their knowledge of molecular biology, Next Generation Sequencing libraries and Illumina library prep and liquid handler automation. | 05/04/2025 |
| 1287 | ImmunityBio El Segundo, CA Clinical Trials Associate Bachelor’s degree Exp: 0-2 years |
Responsible for clinical trials administration to ensure the most effective and efficient conduct of clinical research studies. | 05/04/2025 |
| 1288 | Imricor Burnsville, MN Quality Assurance Engineer Bachelor of science in engineering, science, or technical field Exp: 0-2+ years |
This Quality Engineer position will be responsible for sustaining existing medical device manufacturing lines for heart ablation catheters and associated capital equipment. The Quality Engineer implements, maintains and enforces the internal quality management system to meet ISO standards and FDA quality system regulations. This position develops and implements inspection/validation processes necessary to verify products meet requirements. This position works closely with manufacturing, regulatory, and development to establish/ensure compliance with the quality system throughout the product lifecycle. | 05/04/2025 |
| 1289 | Indivior Raleigh, NC MQA Specialist (2nd Shift) Bachelor’s degree in science, engineering field Exp: 1-3 years |
The Manufacturing Quality Assurance (MQA) Specialist is responsible for providing quality oversight to all manufacturing areas to ensure product quality and SOP/GMP compliance. The MQA Specialist will work closely with production personnel to complete in-process batch record review, resolve batch related issues, and ensure proper good documentation practices. In addition, the MQA Specialist will be responsible for performing routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 05/04/2025 |
| 1290 | Insmed Lebanon, NH Research Associate Bachelor’s degree in biology or related field Exp: 0-2 years |
We are seeking a highly motivated Research Associate to support discovery and development campaigns focused on next-generation biotherapies for serious and unmet medical needs. The candidate will work within the immunology team, conducting in vitro, ex vivo, and in vivo immunoassays on a diverse array of biological drug candidates. | 05/04/2025 |
| 1291 | Insmed Bridgewater, NJ QA Product Quality Complaint Specialis BS in engineering, Life Science or related subject area Exp: 1-2 years |
Overview: Reporting to the Director, Product Quality Complaints, the Product Quality Complaint Associate, QA will play a key role in the complaint process. Specific areas of responsibility include ensuring accurate and thorough complaint intake information, assessing product replacement needs, troubleshooting issues with patients, including on phone support, conducting patient follow ups, supporting product complaint investigations, and tracking and trending complaint data. This position is based in our Bridgewater, NJ HQ (onsite 3 days a week). | 05/04/2025 |
| 1292 | Insmed Lebanon, NH Associate Scientist, Bioinformatics BS in Bioinformatics, Quantitative Biomedical Sciences, Computer Science, Statistics, Mathematics, or a related Exp: 1+ years |
The candidate will be a core member of a computational team developing and applying cutting-edge AI-driven protein engineering methods to design next-generation biotherapeutics, and will work closely with a dynamic and multidisciplinary team conducting associated protein engineering and preclinical analysis experiments. In particular, the role focuses on analysis and modeling of data collected as part of our diverse biotherapeutic development campaigns, with an initial primary focus on data from immunoassays including immunopeptidomics and T cell activation. The candidate will have the opportunity to build and use bioinformatics tools and pipelines to extract information from these rich datasets and thereby help guide design and engineering of life-altering innovative biotherapeutic agents. | 05/04/2025 |
| 1293 | Integer Alden, NY Engineer I Bachelor’s degree in an engineering or related technical field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves general engineering methods and tools. As an entry level engineer, you will ensure that Integer’s internal and external customer expectations are met or exceeded with the direction, instruction and guidance from more experienced engineers and managers in your organization. | 05/04/2025 |
| 1294 | Integer Plymouth, MN Lead R&D Technician Bachelor’s degree Exp: 0-3 years |
The primary purpose of this job is to perform non-routine assignments and provide technical support with a high variety and complexity. Develops, designs, installs, and maintains new processes, tests, and/or control systems. Has critical company knowledge of processes/systems and is responsible for projects and deadlines. Acts as a lead technician in a group. | 05/04/2025 |
| 1295 | Integra LifeSciences Plainsboro, NJ Microbiology Technician I Bachelor’s degree, in Microbiology or Biology Exp: 0-3 years |
The Microbiologist I will provide support to the QC Microbiology Laboratory as pertaining to the respective responsibilities. Performs functions such as executing laboratory testing for in-process and finished good products, water, stability studies, and validation studies as well as performs environmental monitoring. This position is responsible for operating in compliance with all applicable procedures and policies. | 05/04/2025 |
| 1296 | Integra LifeSciences Plainsboro, NJ Microbiologist I Bachelor’s degree, in Microbiology or Biology Exp: 0-3 years |
The Microbiologist I will provide support to the QC Microbiology Laboratory as pertaining to the respective responsibilities. Performs functions such as executing laboratory testing for in-process and finished good products, water, stability studies, and validation studies as well as performs environmental monitoring. This position is responsible for operating in compliance with all applicable procedures and policies. | 05/04/2025 |
| 1297 | Integra LifeSciences Plainsboro, NJ Laboratory Technician II Bachelor’s or Masters Degree Exp: Bachelors: 1-3 years; Master's: 0-2 years |
Reporting to the Lab Operations Manager, Bldg. 104, this position is responsible for performing specialized duties required for the operations of the R&D lab, which includes supporting daily lab operations, assisting in driving lab compliance, supporting EHS compliance monitoring, document control and record management, inventory control, receiving, equipment maintenance, vendor management, technical project executions, and assisting in activities geared towards bio-/chemical safety and lab hygiene. | 05/04/2025 |
| 1298 | Integra LifeSciences Boston, MA Quality Engineer II - Design & Reliability Assurance Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
The Quality Design and Reliability Assurance (DRA) Engineer II is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, specifically the Boston/ Braintree site. The role contributes and supports the design and development of new and improved products. The (DRA) Engineer II will interact with external design and development partners, participating on cross-functional project teams through all phases of the product development process, and assisting the technical team with planning, executing, documenting, and communicating testing activities. The role works with Product Development, Project Management, Regulatory, Marketing and Medical Affairs. | 05/04/2025 |
| 1299 | Integral Molecular Philadelphia, PA Lab Manager, MPA Bachelor's degree in Biology or related field Exp: 1-2 years |
Our close-knit, medium-sized company is composed of smart, curious, diverse scientists who take an active interest in the scientific and technical development of our team members. We are seeking a skilled and organized Laboratory Manager to oversee our cell and molecular biology research and production facility. This role focuses on operational oversight and team management to ensure efficient laboratory operations and support of scientific teams. | 05/04/2025 |
| 1300 | Integral Molecular Philadelphia, PA Research Associate Bachelor’s degree in biology, bioengineering, or a related field Exp: 1-2 years |
Our close-knit, medium-sized company is composed of smart, curious, diverse scientists who take an active interest in the scientific and technical development of our team members. We seek a Research Associate I to join our dedicated group of scientists. A desirable candidate will have the skills to culture mammalian and/or bacterial cells, perform DNA mini-preps, and complete bacterial transformations or cell transfections. | 05/04/2025 |
| 1301 | Integral Molecular Philadelphia, PA Research Technician Bachelor's degree in Biology, Chemistry, medical technology or related field Exp: 6 months |
Our company is in an exciting growth phase where we are launching new products and reaching new markets. To support our growth, we seek a Research Technician to join our Membrane Proteome Array research team. | 05/04/2025 |
| 1302 | Integrated DNA Technologies (IDT) Coralville, IA QA Complaint Analyst Bachelor's degree in Biological Sciences or related field (e.g., Biomedical Engineering, Systems Engineering, Pharmacology, Chemistry) Exp: 1-2 years |
This position is part of the Quality Assurance Department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. In this role, you will have the opportunity to: Contribute to the continuous improvement of product safety +compliance by effectively managing and resolving quality complaints. Communicate with internal team members and external customers to facilitate complaint investigation process. Receive and document complaints from various sources, including customers, healthcare professionals, and internal stakeholders. Work closely with cross-functional teams, including Scientific Application Support (SAS), Quality Assurance, Regulatory Affairs, Product Development, and manufacturing to investigate and resolve complaints. Support quality system investigations, including issue reviews, nonconformances, CAPAs, SCARs, as needed. | 05/04/2025 |
| 1303 | Integrated DNA Technologies (IDT) Coralville, IA Process Development Engineer I Bachelor’s degree in STEM curriculum Exp: 1+ years |
This position is part of the Process Development Department located in Coralville, Iowa and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debates, and are inclusive. Together, we accomplish great things. | 05/04/2025 |
| 1304 | Interius BioTherapeutics Philadelphia, PA Lab Manager, MPA B.S. in Life Sciences Exp: 1-2 years |
As a detail-oriented and thorough Lab Manager, you will be joining a close-knit team that works in sync to ensure our labs are running smoothly. You will be an integral part of the team ensuring the safety of our lab personnel, the fidelity of our data, and the efficient day-to-day operations of our lab space. Bringing your uncanny ability to prioritize for maximum efficiency, your approachable nature, and your appetite to learn, you will be responsible and accountable for several activities from overseeing delivery logistics to tracking and ordering supplies. If knowing that you will never have a boring day in a fast-paced biotech company excites you, then being a part of the Lab Operations team at Interius will not disappoint. | 05/04/2025 |
| 1305 | Iovance Biotherapeutics Tampa, FL Research Associate II Master’s Degree in Cellular Biology, Molecular Biology, Immunology, or related discipline Exp: 0-2 years |
The Research Associate II will support research programs developing methods to optimize the anti-tumor activity of tumor-infiltrating lymphocytes (TILs) for therapeutic applications. A successful candidate will have experience with aseptic cell culture techniques and cell-based immunological assays. Prior experience with processing blood and solid tissue samples, as well as isolation and ex vivo manipulation of T cells and other relevant immune cells is beneficial. This role is a lab-based and will report to Iovance’s Tampa, FL facility. | 05/04/2025 |
| 1306 | Iovance Biotherapeutics Tampa, FL Process Development Associate Master’s in a life science or STEM-related discipline Exp: 0+ years |
The Process Development Associate I will support process development projects and technology transfer activities related to genetically and non-genetically engineered Tumor Infiltrating Lymphocyte (TIL) clinical trials. A successful candidate will have experience with aseptic cell culture techniques and cell-based immunological assays. Prior knowledge of cGMP practices is beneficial in this role. | 05/04/2025 |
| 1307 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I- Microbiology (Night Shift) Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 0-4 years |
The Quality Control Analyst I- Microbiology will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC) and/or iPBMC manufacturing site (IOVA-A). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to complete assigned work. | 05/04/2025 |
| 1308 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I, Microbiology (Wed-Sat Day 7am – 6pm) Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 0-4 years |
The Quality Control Analyst I- Microbiology will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC) and/or iPBMC manufacturing site (IOVA-A). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to complete assigned work. | 05/04/2025 |
| 1309 | Iovance Biotherapeutics Philadelphia, PA MSAT Specialist I B.S degree in a relevant discipline Exp: 1 year |
The MSAT Specialist I is a Manufacturing Operations cell therapy subject matter expert. The MSAT Specialist I reports to the Senior Manager, MSAT and EM and is responsible for manufacturing data analysis, contributing to deviation root cause analysis, and owning steps of the manufacturing process tech transfer. The MSAT Specialist is also responsible for protocol and report authoring, oversight of manufacturing operations, and execution of MSAT laboratory activities. | 05/04/2025 |
| 1310 | Iovance Biotherapeutics Philadelphia, PA Quality Control Compliance Specialist, CAPAs & Change Controls Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-3 years |
Iovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. Iovance is seeking a Quality Control (QC) Compliance Investigator who will in advance and close QC related investigations. Strong technical writing skills are required. Experience in a CAR-T or TIL environment is a plus. The ideal candidate will have experience working in a GMP-regulated laboratory with experience in writing investigations. | 05/04/2025 |
| 1311 | Iovance Biotherapeutics Philadelphia, PA Quality Control Specialist I, Compliance Investigator Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-3 years |
Iovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. Iovance is seeking a Quality Control (QC) Compliance Investigator who will in advance and close QC related investigations. Strong technical writing skills are required. Experience in a CAR-T or TIL environment is a plus. The ideal candidate will have experience working in a GMP-regulated laboratory with experience in writing investigations. | 05/04/2025 |
| 1312 | IQVIA Durham, NC Associate Scientist, Laboratory Operations Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology Exp: 6 months |
We are seeking a Associate Scientistto join Q2 Solutions, IQVIA’s laboratory business at Durham, NC. The Associate Scientistwill perform routine analysis and laboratory testing procedures, ensuring compliance with SOPs and regulatory guidelines while supporting quality assurance and operational efficiency. | 05/04/2025 |
| 1313 | IQVIA Valencia, CA Associate Scientist Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science; medical laboratory technology; or cytotechnology Exp: 6 months |
We are seeking an Associate Scientist to join Q² Solutions, IQVIA’s laboratory business at Valencia, CA. Responsible for conducting routine analysis and laboratory testing procedures while ensuring compliance with SOPs, regulatory guidelines, and quality standards. This position involves data analysis, documentation, and collaboration within a fast-paced laboratory environment. | 05/04/2025 |
| 1314 | IQVIA Valencia, CA Clinical Data Assistant 2 Bachelor’s Degree in chemistry, biology, or medical laboratory technology Exp: 6 months |
The Clinical Data Assistant 2 is responsible for activities including data entry, primary and secondary quality control (QC), and release of RQCQ and EAF requisitions across accessioning platforms. Responsibilities also include managing RITM ticket requests, overseeing secondary passes for special studies, and ensuring team tasks are completed daily. Additional duties may involve the receipt, storage, and shipment of clinical specimens, routine troubleshooting, and guiding entry-level staff on basic department procedures. | 05/04/2025 |
| 1315 | IQVIA Durham, NC Immunoassay Associate Scientist Bachelor’s degree in chemistry or a related field. Exp: 1 year |
As an Immunoassay Associate Scientist, you will execute laboratory experiments with precision, contribute innovatively to scientific procedure design, and uphold the highest standards of Good Laboratory Practices (GLP) for our clients. You’ll not only set up and conduct experiments but also manage laboratory equipment, ensuring protocols are meticulously followed under the guidance of a dedicated lab services manager, researcher, or scientist. | 05/04/2025 |
| 1316 | Jnana Boston, MA Research Associate, Early Discovery Bachelor’s or Master’s degree in Biology, Biochemistry, or a related discipline Exp: 1-2 years |
Jnana Therapeutics is seeking an enthusiastic, highly motivated Research Associate to join our multidisciplinary team. This position offers the opportunity to contribute across Chemical Biology and Compound Management, supporting cutting-edge drug discovery efforts to unlock challenging targets using our novel hit generation platform and a variety of high-throughput, cell-based, and biochemical assays. This is an excellent opportunity for someone excited to grow their career in biotech, gaining exposure to both experimental science and core infrastructure that drives early discovery. | 05/04/2025 |
| 1317 | J-STAR Research Cranbury, NJ Research Scientist of Crystallization R&D MS or BS. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field Exp: 1-5 years |
We are seeking a highly motivated and skilled Research Scientist to join our Crystallization R&D Department at Porton J-STAR. In this role, this position is responsible for leading group or contributing individually to conduct Solid Form Studies and pre-formulation will search for the right solid form and develop formulations to support preclinical and Phase I studies including PK, PD, efficacy, tox studies. This role is also responsible for Crystallization Process Development will develop crystallization processes to define and control final solid form of drug substances with desired solid-state attributes needed for optimum performance as well as drug intermediates for robust purification. The responsibilities of the position include, but are not necessarily limited to, the items listed below. | 05/04/2025 |
| 1318 | Jubilant HollisterStier Spokane, WA Technologist I, Engineering Bachelor’s degree in Engineering, Drafting, or related Scientific or Technical field Exp: 1-5 years |
Holds a general responsibility for projects associated with facilities or production equipment throughout the manufacturing facility. Performs tooling design, maintains engineering drawing system, and tracks production equipment performance to implement efficiency and uptime improvements. Responsibilities may include equipment installation, electrical or mechanical work, equipment optimization, equipment spare parts setup and warehousing, and troubleshooting of equipment. Supports construction activities for various capital improvement projects as required. | 05/04/2025 |
| 1319 | Jubilant HollisterStier Spokane, WA Scientist II, QC (Weekday Day) Bachelor’s Degree in Chemistry, Biology, or related hard science Exp: 1 year |
The QC Scientist II performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw material/product disposition. | 05/04/2025 |
| 1320 | Jubilant HollisterStier Spokane, WA Process Engineer I/II/III/Sr. Bachelor’s of Arts or Science with a major in Biology, Chemistry, Physics, or Engineering Exp: 0-5 years |
The Process Engineer I/II/III/Sr. provides ownership and focus for pharmaceutical processes and technical transfers at Jubilant HollisterStier. This position will engage in and manage projects and multi-disciplinary teams with direct supervision. The process engineer will also contribute technical direction for complex projects and exhibit clear communication skills with all levels of employees. | 05/04/2025 |
| 1321 | Jubilant HollisterStier Spokane, WA QC Scientist I-IV (Weekend Nights) Bachelor of Science in Chemistry, Biology, or related hard science Exp: No Exp |
The QC Scientist I/II/III/IV performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw material, product disposition. In addition, this position demonstrates leadership, teamwork and technical expertise. | 05/04/2025 |
| 1322 | Jubilant HollisterStier Spokane, WA Microbiologist I/II Bachelor of Science in Microbiology or related hard science with microbiology Exp: No Exp |
The QC Microbiologist I-II performs the microbial analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw materials/product disposition. | 05/04/2025 |
| 1323 | Juvena Therapeutics Redwood City, CA Vivarium Research Technician BA Exp: 1-3+ years |
Juvena Therapeutics is seeking a highly motivated Vivarium Research Technician to join our dynamic research team in Redwood City, CA. This role will contribute to the growth of our research portfolio by supporting vivarium operations to advance the development of novel rejuvenating therapies. This position is ideal for a talented, highly motivated and results driven individual who will thrive in a fast-paced, innovative, start-up environment. The individual will report to Senior Scientist/Director in vivo Pharmacology. | 05/04/2025 |
| 1324 | FUJIFILM Diosynth Biotechnologies College Station, TX Quality Assurance-Compliance Specialist II Master’s degree in a related science concentration Exp: 1 year |
The Quality Assurance - Compliance Specialist II - Audit and Inspection will support all associated responsibilities in compliance with FUJIFILM Diosynth Biotechnologies quality policies and site SOPs to ensure regulatory compliance. | 04/15/2025 |
| 1325 | FUJIFILM Diosynth Biotechnologies College Station, TX QA Analyst III Master’s Degree in Biology or Chemistry Exp: 1+ years |
The Quality Assurance (QA) Analyst III, under minimal direction, will be responsible for review and/or approval of basic and technical documentation, drafting and reviewing of internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing product release activities, identifying process and Quality System improvements, and acting as a QA liaison internally and externally. | 04/15/2025 |
| 1326 | FUJIFILM Diosynth Biotechnologies Research Triangle Park, NC Production Technician II BS/BA Exp: 1+ years |
Fujifilm Diosynth Biotechnologies U.S.A., Inc. is seeking a Production Technician II. The successful candidate will be performing glass wash, cell culture sterilization techniques, support mammalian cell culture manufacturing processes, sustaining purification of bio-pharmaceuticals, operate various process equipment, documenting daily manufacturing operations in a cGMP environment, working with single- use and stainless steel bioreactors, fermentation, and/or filtration. | 04/15/2025 |
| 1327 | FUJIFILM Diosynth Biotechnologies College Station, TX Manufacturing Process Engineer I Bachelor’s degree in Science, Engineering, or other related field Exp: 1 year |
The Manufacturing Process Engineer I is an integral part of the Manufacturing Technical Operations department located in College Station, Texas. This position will report directly to the Manager of Technical Operations, Manufacturing. | 04/15/2025 |
| 1328 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Engineer 2, Upstream - MSAT Master’s degree in Engineering, Life Science or Chemical Engineering Exp: No exp |
The Upstream Engineer/Scientist 2 will provide tech transfer support and technical oversight for a large-scale cell culture in monoclonal antibody manufacturing. | 04/15/2025 |
| 1329 | FUJIFILM Diosynth Biotechnologies College Station, TX QA Analyst II Master’s degree in a related science concentration Exp: 1+ years |
The Quality Assurance (QA) Analyst II, under general direction, will be responsible for review and/or approval of basic and technical documentation; Drafting and reviewing of internal Quality policies and procedures; Assisting in and performing product related activities; Assisting in and performing Quality audit functions; Identifying process and Quality System improvements; Acting as a QA liaison internally. | 04/15/2025 |
| 1330 | FUJIFILM Diosynth Biotechnologies College Station, TX Quality Control - Stability Coordinator I Bachelor’s degree in Science, Engineering, or other related field Exp: 1 year |
The QC Stability Coordinator I, will construct, maintain, and oversee the Quality Control Testing of Stability programs to include developing a schedule of pull dates, overseeing testing of each pull, and generating summaries from the data. The Quality Control Coordinator I, under general direction, will be responsible for implementing a Quality Control Stability Program that will encompass the needs of the client for each program. The position will require frequent communication with the Chemistry, Cell Biology, Microbiology, and Quality Assurance groups to coordinate execution of testing, deviation management, and issuance of deliverables. The Coordinator will have visibility to method qualification to ensure timing of stability laydowns. Close attention to detail is required to oversee scheduling the stability testing and compiling data, to facilitate meeting deadlines and milestones. Other responsibilities may include but are not limited to: ownership of CAPA’s and deviations, client meetings, attending planning meetings, communication of changes, and utilizing new software. | 04/15/2025 |
| 1331 | Fulgent Therapeutics Needham, MA Imaging Specialist I Bachelor’s Degree in the Sciences Exp: 1-3 years |
The Imaging Specialist is responsible for performing Quality Control functions on all cases and taking digital microphotographs on designated cases for final pathology report. The Imaging Specialist will follow the direction of the supervisor while taking initiative in performing and promoting quality and efficiency within the department. The Imaging Specialist will be trained in the expected task in order to meet the competency set by the department. | 04/15/2025 |
| 1332 | Garuda Therapeutics Watertow, MA Manufacturing Associate BA/BS degree Exp: 1 year |
Garuda Therapeutics is seeking a motivated Manufacturing Associate or Senior Manufacturing Associate to support routine GMP Manufacturing operations. This includes day-to-day operational tasks including but not limited to Cell Culture in a clean room environment, GMP Materials Logistics, and Environmental Monitoring within Garuda’s GMP manufacturing space. This is an on-site role, primarily in Watertown, MA with occasional work in Cambridge MA. Some travel between sites is required. | 04/15/2025 |
| 1333 | Genezen Indianapolis, IN Analytical Development Laboratory Technician B.S. degree in Biology, Biochemistry, Molecular Biology, or similar field Exp: 1+ years |
We are looking for someone with high emotional intelligence and is comfortable working closely across the team to join us in facilitating the production of viral vectors. The Laboratory Associate I/II will be needed to perform analytical assays for viral vector process development, assist with method development, document experiments, help with lab maintenance and execute assay qualifications. This position calls for an independent thinker who can work seamlessly in a matrixed environment. | 04/15/2025 |
| 1334 | Genezen Indianapolis, IN Manufacturing Technician I/II/III BS degree in Biology, Biochemistry, Molecular Biology, or similar field Exp: 1-5 years |
Responsible for supporting projects from advanced laboratory techniques related to viral vector production and analytics to routine performance of upstream and downstream manufacturing operations including aseptic cell culture technique, preparing solutions and media, molecular biology techniques, chromatography, TFF and general cleanroom sanitization/area maintenance. The position requires working independently, but also under the supervision of experienced personnel. | 04/15/2025 |
| 1335 | Genezen Lexington, MA QC Analyst - Microbiology (Contract) BA or BS in Microbiology or other related science Exp: 0-3 years |
The QC Analyst will be responsible for routine and non-routine QC sampling and testing for the quality of products manufactured for our clients. QC is responsible for execution of the Environmental Monitoring (EM) program in place to monitor Genezen's controlled manufacturing environments (cleanrooms) as well as monitoring of utility systems including Water for Injection (WFI), Pure Steam, Purified Water, Compressed Air and Gas systems. These activities are all performed in accordance with cGMP guidelines and are supported by departmental and interdepartmental policies and standard operating procedures (SOPs). This position is based at Genezen’s state-of-the-art facility in Lexington, MA. This role supports daily operations as well as occasional weekend and holiday operations. This may include but is not limited to in-process monitoring and testing, lot release testing, and stability testing. Supporting activities for quality systems: utility monitoring excursions, non-conformance, deviations, corrective and preventive actions (CAPAs), investigations, Out of Specifications (OOS), and change controls may be required. | 04/15/2025 |
| 1336 | GenScript Pennington, NJ QC Scientist - Microbiology Master’s degree in Microbiology, Molecular Biology, Biochemistry, or related scientific field Exp: 1 year |
The position reports to the Director of QC, is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to lead and evolve this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients. | 04/15/2025 |
| 1337 | GenScript Pennington, NJ Specialist, Bioprocess -Upstream Process Bachelor’s degree in science or engineering Exp: 0-5 years |
The position will work within the Upstream Processing group and performs the following activities while executing upstream operations: Preparation of stock solutions, buffers and media. Filtration of stock solutions, buffers and media. Set-up and operate disposable fermenters / bioreactors and other disposable bioprocess equipment including depth filtration. Passage and expansion of microbial and mammalian cell lines. The position also supports relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 04/15/2025 |
| 1338 | GenScript Redmond, WA EHS Specialist Bachelor’s degree in Engineering or Science Exp: 0-3 years |
We are seeking a Part-Time EHS Specialist. This role reports to the Director of EHS Department and is ideally suited for an individual with an understanding of health, safety and environmental equipment, regulations, and practices. The selected candidate will assist other EHS team members, support the Quality Assurance Function, and assist Facilities Services team with EHS equipment and non-EHS laboratory equipment, operations, and compliance issues. Excellent opportunity for additional learning and development. | 04/15/2025 |
| 1339 | Getinge Wayne, NJ Engineer I, Production Bachelor of Science degree, preferably in Biomedical, Mechanical, Manufacturing Engineering or equivalent Exp: 0-2 years |
The primary responsibility for this Engineer I, Production Engineering position will be reviewing production documentation and addressing deficiencies found, performing equipment qualifications, and other improvements related to compliance issues. Lead and execute process validation requirements in parallel with identifying and implementing improvement and cost elimination projects for manufacturing. This position will report to the Supervisor, Manufacturing Engineering. | 04/15/2025 |
| 1340 | Getinge Englewood, CO Laboratory Technician II, Microbiology BS in microbiology or a related technical discipline Exp: 1-3 years |
Reporting to the Sr. Microbiologist, this position participates in activities related to applied biological research for ongoing analytical studies. Under the guidance of the Sr Microbiologist performs data analysis and communicates findings to the organization. In concert with other disciplines and peers, participates in, and guides the development of, protocols for biological research studies and evaluates alternate methodologies. Recommends materials, supplies, and equipment as required for studies. Develops and participates in the development and validation of both in process and finished product quality test methods. Under the guidance of the Sr. Microbiologist, perform tasks associated with a spore manufacturing process. Perform testing to support process improvement studies, process validation studies, design verification and design validation studies. | 04/15/2025 |
| 1341 | Globus Medical Audubon, PA Electrical Engineer MS in electrical engineering Exp: 1+ years |
We are seeking a highly skilled and motivated Electrical Engineer to join our rapidly growing Digital Health team. You will work closely with a dynamic team of electrical, software, and mechanical engineers to conceptualize and commercialize innovative medical devices to meaningfully impact the lives of patients with musculoskeletal disorders. The ideal candidate will have a strong background designing, building, and testing embedded electrical systems, including firmware design and development. This role requires a balance of creative thinking, analytical design, hands-on prototyping and testing, and systematic product development. | 04/15/2025 |
| 1342 | Globus Medical Methuen, MA Associate Project Engineer, Electrical Bachelor’s degree in electrical engineering Exp: 1-3 years |
Our rapidly growing medical robotics division is searching for enthusiastic electrical engineers wanting to make a difference. Our skillful engineers develop medical robots by working with top surgeons and cross-functional engineering teams. The Electrical Engineer will be part of the electrical team responsible for designing and implementing electronic circuits and electro-mechanical sub-systems for surgical robotic products. The position will be a hands-on one with the individual capable of creative and systematic product development with minimum supervision. | 04/15/2025 |
| 1343 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Microbiology Technician (Weekend Day Shift) Bachelor’s degree in Microbiology or a related field. Exp: 0-2 years |
The QC Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. This position will work Fri-Sun, 6pm-6am. | 04/15/2025 |
| 1344 | Grifols Clayton, NC Validation Engineer I Bachelors Degree in Engineering Exp: 0-2 years |
The Engineer I - Validation / Engineer II – Validation / Validation Specialist I position supports Fractionation, Purification, Filling, Utilities and/or capital projects as required. This position is responsible for assigned qualification and validation related activities related to supporting the Clayton NC site. | 04/15/2025 |
| 1345 | Grifols Clayton, NC Assistant Biologist BS degree in biology, chemistry, or related field Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in SFF and PFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. | 04/15/2025 |
| 1346 | Grifols San Francisco, CA Research Associate Bachelor’s degree in Life Sciences or related discipline Exp: 1 year |
GigaGen, a subsidiary of Grifols, seeks a talented, highly motivated Research Associate to support the process development of our diverse antibody therapeutics pipeline. This will include cell line development, cell culture optimization, and bioreactor production, as well as purification and analytical characterization of antibodies and antibody derivatives. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 04/15/2025 |
| 1347 | Grifols Clayton, NC Associate Stability Research Scientist II BS Degree Exp: 1-2 years |
The incumbent will work in a supporting function to provide scientific and technical assistance in the research and development of plasma derived or recombinant proteins. The position provides support to the Stability Group by overseeing all facets of the stability program that are related to oversight of the stability chamber areas, storage, delivery and documentation of the sample inventory in order to maintain a compliant stability program for licensed products and developmental projects, ensuring on-going safety and quality of our products. | 04/15/2025 |
| 1348 | Grifols Vista, CA Manufacturing Technician 1 Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 04/15/2025 |
| 1349 | Grifols San Diego, CA QC Support Analyst 3 - Blood Typing Solutions B.A. or B.S. in a biological science or chemistry Exp: 0-2 years |
Grifols Diagnostic Solutions Inc is seeking a Quality Control Support Analyst 3 to join our Immunohematology Quality Control department for Reagent Red Blood Cells (RRBC) and Gel Cards in San Diego, CA. This position will be reporting to the QC Supervisor. The primary job function of the QC Support Analyst 3 is to test and release raw materials, sub-assemblies or finished goods. In order to be successful in this role, candidates must have a bachelor’s degree in Biological Sciences or Chemistry with 0 to 2 years of relatable QC experience. Experience working and handling blood products, preferred. | 04/15/2025 |
| 1350 | Grifols Clayton, NC Engineer - Global Process Engineering Bachelor's Degree in Engineering or related field. Exp: 0-2 years |
The Process Engineer demonstrates consistent application of technical knowledge and/or regulatory knowledge in the Process Engineering discipline. Develops and implements solutions. Leads projects of larger scope (or portions of projects) and is often called upon by peers for guidance. Directs project or discipline teams. Meets customer needs in support of business goals. | 04/15/2025 |
| 1351 | Guardant Health Redwood City, CA Biospecimen Associate I (Thursday- Saturday) Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field Exp: 1-2 years |
The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow. | 04/15/2025 |
| 1352 | Guardant Health Redwood City, CA Clinical Laboratory Associate II (Tuesday-Saturday) Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field Exp: 1 year |
The Clinical Laboratory Associate (CLA) II is responsible for supporting the daily operations of the Clinical Laboratory and assisting the Clinical Laboratory Scientist (CLS) during patient testing. In addition to the primary role of CLA, there will be a need to provide back-up support to the other groups (Reporting, Biospecimen Management, QC, etc.). The CLA II may serve as a lead to the CLA team to coordinate tasks, divide workload, manage equipment usage schedule and documents reviewing/filing process as assigned. The CLA II has demonstrated the skills and competency to assist the CLSs in automated sample processing and in all other support functions. | 04/15/2025 |
| 1353 | Guardant Health Redwood City, CA Biospecimen Associate I (Monday-Friday) Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field Exp: 1-2 years |
The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow. | 04/15/2025 |
| 1354 | Guardant Health Redwood City, CA Clinical Laboratory Associate II (Sunday-Tuesday) Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field Exp: 1 year |
The Clinical Laboratory Associate II (CLA II) is responsible for supporting the daily operations of the Clinical Laboratory and assisting the Clinical Laboratory Scientist (CLS) during patient testing. In addition to the primary role of CLA, there will be a need to provide back-up support to the other groups (Reporting, Biospecimen Management, QC, etc.). The CLA II may serve as a lead to the CLA team to coordinate tasks, divide workload, manage equipment usage schedule and documents reviewing/filing process as assigned. The CLA II has demonstrated the skills and competency to assist the CLSs in automated sample processing and in all other support functions. | 04/15/2025 |
| 1355 | Guardant Health Redwood City, CA Clinical Laboratory Associate II (Wednesday-Saturday) Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field Exp: 1 year |
The Clinical Laboratory Associate II (CLA II) is responsible for supporting the daily operations of the Clinical Laboratory and assisting the Clinical Laboratory Scientist (CLS) during patient testing. In addition to the primary role of CLA, there will be a need to provide back-up support to the other groups (Reporting, Biospecimen Management, QC, etc.). The CLA II may serve as a lead to the CLA team to coordinate tasks, divide workload, manage equipment usage schedule and documents reviewing/filing process as assigned. The CLA II has demonstrated the skills and competency to assist the CLSs in automated sample processing and in all other support functions. | 04/15/2025 |
| 1356 | HemoSonics Durham, NC R&D Engineer Master’s degree in Engineering or related discipline Exp: 0 years |
Being able to wake up in the morning knowing that your work makes a difference in the lives of others - that's the best kind of motivation. If you're looking for a company where you can combine a passion for improving patient care and outcomes with the skills and experience you've spent a career developing, then HemoSonics may just be your perfect fit! This role is on-site in Durham, North Carolina - working remotely from other parts of the country is not an option for this role, so all candidates must be local or planning to move for this position. | 04/15/2025 |
| 1357 | Hesperos Orlando, FL Engineer Associate I/II Bachelor’s degree of Engineering Exp: 1 year |
You are experienced in software development for scientific data and scientific equipment, and developing algorithms, software, and interfaces. You are conscientious and pay almost obsessive attention to detail, as organized documentation is second nature. You are curious, love learning, and are eager to take on hard problems. You thrive in a fast-paced environment and enjoy pushing the edge of what is possible. You are resourceful and like to work independently but are not shy to ask for advice. You are a cross-disciplinary team member, who is excited to work with and learn from other engineers, biologists, chemists, modelers, and experimentalists. You are comfortable communicating across teams. You deliver. You know that what matters is delivering a solution that works every time. | 04/15/2025 |
| 1358 | HighRes Beverly, MA Associate Manufacturing Engineer Bachelor's degree in Mechanical or Manufacturing Engineering Exp: 0-2 years |
The Associate Manufacturing Engineer will primarily be focused on creating and implementing process improvements and strategies to optimize manufacturing efficiency. This includes sustaining, continuous improvement, and new product introduction efforts to scale with the dynamic workload. They will also be working together with the technician workforce to provide production floor support, as well as being a cross-functional resource to liaison between operations and other engineering teams to ensure communication and compliance across all facets of manufacturing. | 04/15/2025 |
| 1359 | HighRes Remote, CA Jr. Field Service Engineer Bachelor’s degree in electromechanical/life science/engineering Exp: 0-3 years |
The Field Service Engineer position at HighRes Biosolutions is the primary role responsible for installation, maintenance, troubleshooting and repair of systems and devices at customer sites. This position specializes in the hardware aspect of the products, coordinating with the Automation Support Engineer role in Customer Support and collaborating with the manufacturing and commissioning department (software and configuration-focused) for full coverage support of the products. Levels I and Junior are roles for carrying out Field Service Engineer responsibilities in either learning or assisted modes, with oversight and assistance from a team lead, supervisor, manager, or skilled technical Customer Service colleague(s). | 04/15/2025 |
| 1360 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro BS/BA Degree in Microbiology or Biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management. | 04/15/2025 |
| 1361 | Hikma Cherry Hill, NJ Manufacturing Specialist - 2nd Shift B.S. in technical discipline Exp: 0-3 years |
The Manufacturing Specialist will assist the shift lead in a hands-on approach to overseeing production activities including, filling, sterilization, component and equipment prep, and compounding. Completes quality systems activities including commitments, deviations, DCEs, and SOP revisions as necessary. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing recommendations. Interprets manufacturing policies, procedures, and programs | 04/15/2025 |
| 1362 | Hikma Cherry Hill, NJ QA Inspector Bachelor’s Degree in Science or equivalent Exp: 0-2 years |
The QA Inspector monitors in-process product quality for Filling and Inspection and Packaging of parenteral products. The QA Inspector performs visual and functional testing of products against statistically based sampling plans. In addition, the QA Inspector performs routine inspection and testing of components following Standard Procedures and specifications as required by production schedules. In performing the above duties, the individual is responsible for accurately and clearly documenting test results following cGMPs. This position participates in rotation for weekend coverage and as needed during the work week. | 04/15/2025 |
| 1363 | ICU Medical Southington, CT Engineer I, Quality Bachelor’s degree in Engineering or STEM Exp: 0-2 years |
Engineer I, Quality will support the ICU Quality Operations Department and report to the Quality Operations Manager. They are responsible for sustaining manufacturing and validations through adherence to established design control processes, good quality and documentation practices. The key responsibility of this position is to exercise judgement and act while adhering to defined quality procedures during project support & improvement. Engineer I, Quality will complete basic projects assigned by more experienced engineers and managers. They work on projects/matters of limited complexity in a support role while being closely managed. | 04/15/2025 |
| 1364 | Emerald Cloud LAb Austin, TX Laboratory Operations Shift Manager Bachelors or master’s degree in industrial engineering Exp: 1-4 years |
As a Shift Manager, you will be responsible for managing a shift of approximately 15-20 individuals. As the leader of this team, you will be responsible for setting high standards for your shift while ensuring all performance metrics are met on time and within cost. In this role you’ll act as a key business partner to operations leadership and cross-functional partners, assisting with driving efficiency and implementing scalable processes. This position requires a results-oriented, high-energy individual with the stamina and mental agility to thrive in a fast-paced startup environment. | 04/07/2025 |
| 1365 | Emerald Cloud LAb Austin, TX Laboratory Operator I, II, & III Bachelor’s degree Exp: 1-3 years |
The demand for our service is growing, and to meet that demand, we are recruiting Lab Operators looking to explore opportunities in the biotech space and grow with our organization. Qualified candidates will receive comprehensive lab and safety training, allowing them the ability to run protocols in our Austin facility. These protocols are critical to sustaining the high-quality operations of the facility and provide experience working in ECL’s unique, process-driven lab environment with our integrated software tools. | 04/07/2025 |
| 1366 | Empirico Madison, WI Assistant Scientist - Drug Discovery Bachelor’s degree in Molecular Biology, Biochemistry or a related discipline Exp: 1 year |
Empirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines, is looking for a talented scientist to help advance our growing pipeline. This position offers a unique opportunity to participate in and support multiple projects in diverse therapeutic areas, across different stages of preclinical development. You will work closely with other scientists that have a passion for finding novel approaches toward the treatment and prevention of disease. | 04/07/2025 |
| 1367 | Empirico Madison, WI Assistant Scientist / Associate Scientist - CMC Bachelor’s degree in Chemistry or Chemical Engineering with an understanding of organic and analytical chemistry Exp: 1-3 years |
Empirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines, is looking for a chemist with an interest in solid-phase oligonucleotide synthesis and analytics. This is an excellent opportunity for a highly motivated, creative scientist to be a vital member of our team. | 04/07/2025 |
| 1368 | Empirico Madison, WI Scientist / Senior Scientist - Oligonucleotide Chemistry Master’s degree in Organic Chemistry Exp: 1-7 years |
Empirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines, is looking for a talented chemist with experience in solid-phase oligonucleotide synthesis and analytics. This is an excellent opportunity for a highly motivated, creative scientist to be a vital member of our team. | 04/07/2025 |
| 1369 | Endo Rochester, MI Chemist II, Quality Control Laboratory Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 04/07/2025 |
| 1370 | Endo Rochester, MI Microbiologist I Master of Science degree in microbiology, biology or related field Exp: 1+ years |
Performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 04/07/2025 |
| 1371 | Endo Rochester, MI Operations Engineer, Sterile Fill (afternoon) Bachelor’s Degree or higher in Engineering or Science related equivalent Exp: 1-3 years |
The Operations Engineer, Sterile Filling, works in a hands-on capacity in a fast-paced, cGMP environment and production support areas to process sterile and aseptic products. The specialist works in collaboration with Operations, Maintenance, Engineering, Supply Chain, Quality Assurance, and Pharmaceutical Technology and Validation for successful repeatable day-to-day manufacturing operations in the Sterile Filling Area. Position is responsible for working with operations team to mitigate gaps within the sterile filling operations. Position also facilitates maintaining departmental documentation and processing of batch documentation. Position is also trained to perform verification of process steps in support of departmental supervision. Knowledge of cGMP’s is essential to successful performance of the position. In partnership with the site leaders sponsors a quality and compliance focused site culture which embraces RFT (right first time) and CI (continuous improvement) expectations. | 04/07/2025 |
| 1372 | Endo Horsham, PA QC Analyst I - Microbiology B.S. in a Biological Science or related field Exp: 0-3 years |
The QC Analyst I – Microbiology will perform microbiological testing, release of in-process, intermediates and finished products, and testing for validation purposes. This role completes appropriate documentation to support testing procedures including data capture forms, equipment logbooks, and inventory forms. Additionally, this role is responsible for assisting with the writing of standard operating procedures (SOPs) and revision of existing documentation. | 04/07/2025 |
| 1373 | Endo Rochester, MI Quality Associate Specialist, Product Release BA/BS degree in a related discipline Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 04/07/2025 |
| 1374 | Endo Rochester, MI Operations Engineer, Sterile Filling (Days) Bachelor’s Degree or higher in Engineering or Science related equivalent Exp: 1-3 years |
The Operations Engineer, Sterile Filling, works in a hands-on capacity in a fast-paced, cGMP environment and production support areas to process sterile and aseptic products. The specialist works in collaboration with Operations, Maintenance, Engineering, Supply Chain, Quality Assurance, and Pharmaceutical Technology and Validation for successful repeatable day-to-day manufacturing operations in the Sterile Filling Area. Position is responsible for working with operations team to mitigate gaps within the sterile filling operations. Position also facilitates maintaining departmental documentation and processing of batch documentation. Position is also trained to perform verification of process steps in support of departmental supervision. Knowledge of cGMP’s is essential to successful performance of the position. In partnership with the site leaders sponsors a quality and compliance focused site culture which embraces RFT (right first time) and CI (continuous improvement) expectations. | 04/07/2025 |
| 1375 | Enovis Carlsbad, CA Test Engineer Bachelor’s degree in engineering (Mechanical or Biomedical) Exp: 1+ years |
Test Engineer is responsible for designing, developing, and testing mechanical systems and components. The engineer is responsible for producing and implementing designs and test procedures analyzing and troubleshooting mechanical systems and components and developing and testing prototypes. The engineer will participate in daily technical meetings to review project progression, performance of team members and recourse management. This position will serve as great transition from education to junior level for a young professional to further engineering skills in an array of projects. | 04/07/2025 |
| 1376 | Eurofins West Point, PA Lab Coordinator BS degree in Biology, Chemistry, Engineering, or related sciences Exp: 0+ years |
Performs routine checks on equipment to verify parts are in good condition, ensures equipment is functioning properly, and documentation and recordkeeping is maintained, Arranges equipment replacement and repairs as needed, Coordinates with laboratory staff, and safety to properly maintain and remain compliant in common/shared equipment including preventive maintenance (PMs), service, repair, calibration, and certification, Ordering new equipment, Prepares purchase requests, obtains quotes and interacts with purchasing personnel, Schedules and coordinates instrument installation, Facilitates instrument/equipment training with lab staff, Supporting Lab staff with lab maintenance, Freezer/ fridge maintenance, Benchling Inventory compliance, Shared reagent/ biologics inventory, Maintain/ order supplies in compliance with ‘hazardous materials’ (COSMIC), Submitting shipment requests- within and outside of the facility | 04/07/2025 |
| 1377 | Eurofins Indianapolis, IN Analytical Biochemist Bachelor's degree in biology, biochemistry, chemistry, or other related degree concentration Exp: 1-2 years |
Perform biochemical testing on samples including, but not limited to HPLC, CE, and physical properties, Use ALCOA to document test results in electronic notebooks. | 04/07/2025 |
| 1378 | Eurofins Portage, MI Scientist Bachelor's degree in biology, chemistry, or other related degree concentration Exp: 1-2 years |
Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health product, Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus, Executing method transfer protocols, Performing monthly maintenance of laboratory equipment, Working efficiently, documenting work clearly, and performing tests accurately, Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations, Reads and understands analytical procedures (compendial and client supplied) and internal SOPs, Processes data, generates reports, and evaluates data, Trains others in laboratory procedures, Performs laboratory maintenance, Communicates with vendors and repair personnel, Writes investigations, Leads project/test areas and perform method transfers/feasibility studies, Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus | 04/07/2025 |
| 1379 | Eurofins Lexington, MA Bioassay Scientist MS in Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration Exp: 6 months |
We are seeking a scientist with strong organizational skills, excellent oral and written communication, and keen attention to detail. The ideal candidate will support the development, optimization, and qualification of analytical methods in a compliance-based environment. This role involves method development, process support, documentation, and potential technology transfer, along with some analytical testing. The ability to work independently and collaboratively, along with self-motivation, adaptability, and a positive attitude, is essential. | 04/07/2025 |
| 1380 | Eurofins Frederick, MD Sample Management Technician, 2nd Shift BS degree in a science-related field Exp: 1-2 years |
We seek a highly motivated and detail-oriented Laboratory Technician to join our team. The successful candidate will possess a fundamental understanding of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs), ensuring compliance with industry standards on a daily basis. The role requires proficiency in laboratory operations, sample management, and collaboration across departments. | 04/07/2025 |
| 1381 | Eurofins Frederick, MD Sample Management Technician, 1st Shift BS degree in a science-related field Exp: 1-2 years |
We seek a highly motivated and detail-oriented Sample Management Technician to join our team. The successful candidate will possess a fundamental understanding of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs), ensuring compliance with industry standards on a daily basis. The role requires proficiency in laboratory operations, sample management, and collaboration across departments. | 04/07/2025 |
| 1382 | Eurofins Lancaster, PA Scientist - Small Molecule Analytical Chemistry Master's degree in chemistry, pharmaceutical science, or other related degree concentration Exp: 1 year |
Eurofins' BPT Small Molecule Method Development and Validation team is seeking an Scientist to join their team full time in Lancaster, PA. This individual will work in a duel analyst and data reviewer role. | 04/07/2025 |
| 1383 | Evonik Birmingham, AL Microbiology Lab Technician Bachelor’s degree in microbiology, biological sciences, or related field of study Exp: 1 year |
This position is responsible for conducting routine microbiological testing, documentation, and data analysis, of utilities, raw materials, facilities and equipment. Additionally, the microbiology technician will be responsible for upkeep of the laboratory, laboratory supplies, and other various routine laboratory tasks. | 04/07/2025 |
| 1384 | Evonik Birmingham, AL Manufacturing Specialist BA/BS Degree in STEM subject Exp: 0-2 years |
The Manufacturing specialist acts as primary production process owner and subject matter expert (SME) for manufacturer of final products in Birmingham Labs, PDS Services. Responsibilities include managing procedures, batch documentation, data and information, reporting and analysis. Short term growth of staff working in assigned area and unit operations: assure technical knowledge, proficiency, and compliance is embedded as part of training, training material, GMP documentation, job aids, and others as needed. | 04/07/2025 |
| 1385 | Evonik Birmingham, AL Associate Scientist Bachelor’s degree in Chemistry or other relevant science Exp: 0-3 years |
This position is responsible for completing project tasks; and serving as the Quality Control contact on one or more projects by carrying out laboratory experiments, completing assignments that are varied in nature, contributing to report writing and representing SurModics at meetings with customers. | 04/07/2025 |
| 1386 | Evonik Bayport, TX Lab Technician I Bachelor's Degree in chemistry or related scientific or engineering fields. Exp: 1 year |
The Lab Technician will conduct analytical, chemical, and physical laboratory tests to assist scientists and engineers in making qualitative and quantitative analyses of solids, liquids, and gaseous materials for research and development of new products or processes, quality assurance and control, maintenance of environmental standards, and other work involving experimental, theoretical, or practical application of chemistry and related sciences. | 04/07/2025 |
| 1387 | Evonik Birmingham, AL Plant Engineer I BS/MS in an engineering field including but not limited to Mechanical, Electrical, Industrial, Chemical, or Biomedical Engineering Exp: 1-3 years |
The Plant Engineer I acts as system owner and subject matter expert (SME) for assigned area(s) to include but not limited to infrastructure, utilities, and process equipment. He/ She will ensure that the assigned systems are in a state of operational readiness by ensuring that preventive maintenance is carried out on time and in full, any issues are documented and investigated, corrective and preventive actions are implemented. He/ She provides technical expertise to maintain and continuously improve assigned areas to improve reliability, reduce downtime, minimize costs and ensure technical means for safe and high-quality operation. | 04/07/2025 |
| 1388 | Evotec Seattle, WA QA Specialist Bachelor's Degree in Biochemistry, Biology, Microbiology, Chemistry, or a Scientific/Engineering degree Exp: 1 year |
This role is responsible for the execution of day-to-day QA responsibilities for GMP manufacturing, along with building and enhancing the quality assurance systems. The role incumbent works both independently and collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. | 04/07/2025 |
| 1389 | Exact Sciences Madison, WI Metrology Associate I Bachelor’s degree in technology, electronics, mechanical engineering, computer science, Molecular Biology or related field Exp: 1+ years |
The Metrology Associate I will service custom and off-the-shelf laboratory instrumentation and equipment. This role will be responsible for, assembly, installation, calibration, routine maintenance, investigation and diagnosis of failures, repair, requalification, and filing service reports. The Metrology Associate I will work with colleagues to ensure proper instrument function and maintenance. | 04/07/2025 |
| 1390 | Exact Sciences Madison, WI Calibration Lab Technician I Bachelor’s degree in Electronics, Molecular Biology, or related field Exp: 1+ years |
The Calibration Lab Technician I is responsible for performing calibration, maintenance, and repair on a variety of equipment sent into the calibration lab (e.g., pipettes (single & multi-channel), bottle top dispensers, load cells, masses, timers, temperature measuring equipment, etc.). This role will demonstrate a high level of organization, the ability to multitask and build trust with internal and external customers. | 04/07/2025 |
| 1391 | Exactech Gainesville, FL Manufacturing Engineer Bachelor's degree Exp: 1-3 years |
Create and maintain the lowest cost, highest quality machining & manufacturing processes, tooling and supporting documentation for all parts produced. | 04/07/2025 |
| 1392 | Excellos San Diego, CA Cell Therapy Manufacturing Associate I or II Bachelor’s degree in cell biology or related field Exp: 1+ years |
The Manufacturing Associate I or II, Tissue and Cell Therapy is responsible for performing well regulated GMP aseptic cell culture activities including media preparation, cell thaws, cell expansion, cell harvesting, and cryopreservation using standard cell culture technologies in a cleanroom environment. The Associate will be responsible for following Batch Production Records, Standard Operating Procedures, and work instructions in manufacturing spaces. The Associate will be responsible for participating in the maintenance of critical supplies, equipment, product testing, product storage and product distribution. | 04/07/2025 |
| 1393 | EyePoint Watertown, MA Process Engineer I (Manufacturing) Bachelor of Science, Engineering Exp: 1-2 years |
EyePoint is seeking a motivated Process Engineer I with excellent interpersonal skills to join our team. This person will be responsible for process sustaining and improvement of all components, device and packaging related projects. This position requires the application of continuous improvement, equipment oversight, trending, layout plans, testing, data analysis and report writing to resolve and improve manufacturing efficiencies. Candidate must be able to effectively collaborate with internal R&D, Quality, Regulatory and Operations departments and with external vendors and suppliers to deliver against project timelines and maintain process sustaining activities. The ideal candidate possesses the ability to develop credibility and trust as a technical resource to contribute to the company’s growth, productivity, and innovation. | 04/07/2025 |
| 1394 | Flamma Group Malvern, PA Associate Process Scientist BS or MS in Organic Chemistry Exp: 0-1 years |
Execute laboratory experiments. Assist in determining operational space for various process parameters to ensure efficient and succesful scale up. Help evaluate safety of processes utilizing calorimetry data and stability data to fully understand the hazards and the trigger points of these hazards. Follow guidance from senior scientists or project leader to problem solve complex synthetic problems during development. Assist in scale up of processes in the kilo labs. Support scale up of processes in the pilot plant in a GMP environment. Collaborate with analytical chemists to complete work assignments. Contribute to laboratory organization. Accurately collect reliable data in the form of lab procedure or reports to be used for updates to customers or during drafting of production's MBR. | 04/07/2025 |
| 1395 | Fresenius Kabi North Andover, MA Engineer, Test (Medical Device) Bachelor’s degree in Engineering (Mechanical, Computer, Biomedical or related) Exp: 1-3 years |
The Engineer, Test (Medical Device) assists with all phases of systems performance verification and validation activities for infusion devices to support product development, product changes, and regulatory submissions. This includes prototype evaluations, planning, and execution of informal and formal verification cycles and reporting. | 04/07/2025 |
| 1396 | Fresenius Kabi Melrose Park, IL Packaging Engineer - Nights Bachelor’s degree in Engineering (Electrical, Mechanical, Automation, Controls, Computer, etc.) Exp: 1-3 years |
The Packaging Engineer will be responsible for using technical expertise in support of daily operations in packaging operations by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity. Apply accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyze situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 04/07/2025 |
| 1397 | Fresenius Kabi Melrose Park, IL Manufacturing Engineer Bachelor’s degree in Engineering (Electrical, Automation, Controls, Computer, Mechanical, etc.). Exp: 1-3 years |
The Manufacturing Engineer uses knowledge and technical expertise in support of daily operations within aseptic filling by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity, all under guidance of Sr. Engineers or Production Management. Applies accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyse situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 04/07/2025 |
| 1398 | Fresenius Kabi Wilson, NC Validation Engineer BS/BA degree in science, engineering, manufacturing technology or closely related field Exp: 1-3 years |
Responsible for providing technical support to operations in terms of equipment/system initial validation and equipment/system requalification’s. Will participate in equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. The individual must have a comprehensive understanding of cGMPs and become certified to enter Controlled Areas of the plant (Grade D, C and up to B/ A). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 04/07/2025 |
| 1399 | Fresenius Kabi Melrose Park, IL Scientist I B.S. in Chemistry, Biology or related physical science Exp: 1-4 years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 04/07/2025 |
| 1400 | Fresenius Kabi Melrose Park, IL Scientist, Analytical Development MS degree in Chemistry or related field Exp: 0-3 years |
The Scientist, Analytical Development conducts all aspects of Analytical Development including method development, experimentation, and record keeping. The incumbent must be able to develop and implement methods that meet project needs. The position is responsible for conducting analytical development studies with increasing complexity in nature and solving problems to ensure a robust method can be performed in the laboratory. | 04/07/2025 |
| 1401 | Freudenberg Carpinteria, CA Quality Engineer I - Inhealth Technologies Bachelor’s degree in Engineering, Sciences or related discipline Exp: 1+ years |
Reviews/ approves Design Control documentation (e.g. Design Verification, Process, or component validation), Leads Test Method validation activities associated with Design Verification activities, Represents Quality in New Product Development (NPD) project team meetings & Design Reviews, Prepares and releases Inspection Plans and Quality Control Inspection Criteria (QCICs) that supports qualification of purchased components, Audits Design & Development activities to ensure compliance with procedures and standards, Supports Risk Management activities for new or legacy products. This includes Risk Management Planning (RMP), Risk Analysis including post-market risk assessments, create Risk Management Reports, Leads complaint investigations and trend reporting for InHealth Technologies (IHT) products, Analyze internal and external quality product performance trends and address non-conformities, Represent Quality engineering in Engineering Change Order process for IHT products, Participates in both Internal and/or External audits, Participates in any product recalls or field actions | 04/07/2025 |
| 1402 | Freudenberg Jeffersonville, IN Manufacturing Engineer I Bachlors Degree in Technical Discipline (Mechanical, Manufacturing, Mechatronics or Biomedical). Exp: 1-3+ years |
Lead the identification, development, and qualification of manufacturing processes improvements. Deploy GROWTTH® tools to create simple, robust, and innovative manufacturing processes for new and sustaining products. Create and maintain quality system documentation such as process failure mode effects analysis, process flow charts, process validation plans, validation protocols, manufacturing procedures, etc. Supports the development and use of all production and control related processes and documentation including APQP, Control Plans, Qualification Plans, Engineering Change, Deviations, Corrective and Preventative Actions, DFMEA, PFMEA, PPAP, FAI, DFMA, and SPC tools. Identify and establish new processes and technologies necessary to achieve best cost targets. Provide coaching, and guidance regarding project tasks to other engineers, designers, technicians and associates. | 04/07/2025 |
| 1403 | Frontage Laboratories Exton, PA Associate Scientist Bachelor’s or master’s degree in Biochemistry, Molecular Biology, Immunology, Pharmaceutical Sciences, or a related field. Exp: Entry Level |
We are seeking a highly motivated and detail-oriented Associate Scientist to join our Pharmacokinetics (PK) group. The successful candidate will support bioanalytical method development, validation, and sample analysis using ligand binding assays (LBA) to assess pharmacokinetics for preclinical and clinical studies. This role requires expertise in bioanalytical techniques, data analysis, and regulatory compliance. | 04/07/2025 |
| 1404 | Contract Pharmacal Corp Hauppauge, NY Scientist I; Analytical R&D Bachelor’s or Master’s degree in chemistry or analytical chemistry Exp: 1-2 years |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. | 03/31/2025 |
| 1405 | Contract Pharmacal Corp Hauppauge, NY Chemist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Chemist is responsible for and has experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Microbiology, ICP, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 03/31/2025 |
| 1406 | Contract Pharmacal Corp Hauppauge, NY Microbiologist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Microbiologist is responsible for and has experience in performing microbial analysis for the QC Microbiology laboratory which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 03/31/2025 |
| 1407 | Cook Medical Winston-Salem, NC Sustaining Engineer MS in Engineering or Engineering Technology Exp: 1 year |
The primary purpose of this position is to lead projects to design, test and technically document design and/or process changes required for the maintenance of released medical devices. | 03/31/2025 |
| 1408 | Cook Medical Bloomington, IN Sterility Assurance Specialist I Bachelor's degree in Engineering, Microbiology, Biology, or related field Exp: 1-2 years |
The Sterility Assurance Specialist I at Cook Incorporated is responsible for multiple projects/tasks related to ensuring continued compliance with sterilization validation and product adoption requirements. The Sterility Assurance Specialist will collaborate on cross-functional teams to perform necessary tasks relating to product/process change evaluations, sterilization validations, product adoption, and assurance of sterility requirements. | 03/31/2025 |
| 1409 | Cook Medical Bloomington, IN Sr. Global Sustaining Engineer Bachelor's degree in Engineering, Microbiology, Biology, or related field Exp: 1-2 years |
Senior Engineer, Sustaining, will perform activities related to sustaining commercially available products. These activities may include (but are not limited to) product/process remediation, risk analysis, regulatory approval support, and product/process improvements. The Senior Engineer works independently with limited supervision on complex activities and projects. The Senior Engineer acts as a mentor and leader in the department and may review/approve the work of less experienced engineers and/or contractors. This is a Global Sustaining Engineering position. | 03/31/2025 |
| 1410 | CooperSurgical Livingston, NJ Laboratory Services Specialist II Bachelor’s or Master’s Degree in Biology or other related science Exp: 1 year |
Performs complex molecular-based procedures on clinical samples with a high degree of quality and in accordance with standard operating procedures. Analyzes clinical results and provides diagnoses. Communicates and collaborates with other professionals within the company and clients, as needed • Properly uses and maintains laboratory equipment. Performs clerical tasks associated with clinical cases, including but not limited to: maintenance of specimen and case logs, preparation/documentation of assay worksheets, preparation of analysis sheets and clinical reports. Receives and verifies clinical samples. Witnesses hands-on clinical procedures. Participates in lab maintenance (i.e. cleaning, annual/bi-annual/monthly maintenance of equipment, unpack supplies, etc.). Complies with Safety Standards and Good Lab Practices. Performs additional duties or assignments as directed by management. | 03/31/2025 |
| 1411 | CooperSurgical Los Angeles, CA Laboratory Technician II Bachelor's degree in Science Exp: 1-2 years |
Maintains demonstrated proficiency with all applicable Standard Operating Procedures. Performs semen evaluations to screen, process, and preserve for future clinical use. Execute an array of laboratory procedures including but not limited to: Daily setup of all laboratory equipment and daily QC. Intrauterine (IUI) and intracervical (ICI) insemination semen preparation. Sample Qualification- post-thaw sample analysis with both manual and automated analysis. Preparation of bodily fluid including blood, urine, and semen packing for specimen transport to reference laboratories. Cryogenic procedures including routine liquid nitrogen storage-tank verifications, internal vial transfers between tanks, vial quality control checks, preparing samples and shipping containers for vial movement. Conducts and accurately records all required daily, monthly and yearly quality control checks; responds with corrective action when needed. Communicates any errors, accidents or incidents to Management and records in associated tracking and record logs. Performs routine cleaning of laboratory equipment. Complies with all regulatory, quality assurance, quality control, standard operating, and safety procedures to audit-ready standards. Completes Bi-annual and annual proficiency and competency assessments. Participates in the review of standard operating procedures. Responsible for aliquoting and maintaining necessary aliquot-inventory levels for all media to maintain production. Responsible for lab supply maintenance. Performs all necessary opening and closing duties. Provides coverage for donor related tasks such as identification and qualification as needed. Always while ensuring privacy and maintaining the utmost professionalism. May perform phlebotomy if licensed. Other duties and projects as required. | 03/31/2025 |
| 1412 | Corden Pharma Boulder, CO QC Analyst - Temp Bachelor's Degree Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 03/31/2025 |
| 1413 | Corden Pharma Boulder, CO QC Analyst - Days Bachelor's Degree Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 03/31/2025 |
| 1414 | Corden Pharma Boulder, CO QC Analyst - Nights Bachelor's Degree Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training Manual. Maintains a high level of housekeeping and attention to detail. | 03/31/2025 |
| 1415 | Crown Bioscience San Diego, CA Research Associate, In vivo Bachelor's degree Exp: 6 months |
The purpose of the In Vivo Research Associate I position is to provide support on In vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 03/31/2025 |
| 1416 | CSL Schenectady, NY Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1417 | CSL Huntsville, AL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1418 | CSL Portage, MI Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1419 | CSL Springfield, IL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1420 | CSL Kankakee, IL QAO Specialist I B.A. or B.S. degree preferably in scientific or technical field (e.g., chemistry, biology, physics, engineering, computer science, technical writing) Exp: 0-2 years |
This is an entry level position into Quality Assurance Operations. Developing responsibilities include assisting with investigating deviations, relevant to area of responsibility. Responsible for driving continuous improvement on production floor to ensure compliance to cGMPs. Real time review of batch records, including critical processing steps with production floor presence. | 03/31/2025 |
| 1421 | CSL Waukegan, IL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1422 | CSL Fairfield, CA Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1423 | Curia Springfield, MO Quality Control Analyst I Bachelor’s degree in Chemistry or related field Exp: 0-3 years |
The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications. | 03/31/2025 |
| 1424 | Curia Albuquerque, NM Microbiologist I Bachelor’s degree in a scientific discipline, preferably microbiology or related field Exp: 1 year |
The Microbiologist I is responsible for performing microbiological testing and quality activities to support product production, environmental monitoring, and product release in a pharmaceutical manufacturing environment. This role ensures compliance with regulatory requirements and company standards by conducting microbiological assays, analyzing trends, and accurately documenting and reporting results. The QC Microbiologist I collaborates with cross-functional teams to identify potential microbiological risks, troubleshoot deviations, and contribute to continuous improvement initiatives to maintain product quality and patient safety. | 03/31/2025 |
| 1425 | Cynosure Westford, MA Regulatory Specialist BS or BA in engineering or scientific field Exp: 1-2 years |
Responsible to be a Member of the Regulatory team that ensures regulatory approvals are effectively obtained and compliance with regulations is maintained. The specialist may participate in product development teams. Author regulatory submissions and technical files. Organize regulatory information and tracks and controls submissions. Review and advise on labeling for compliance with regulatory filings. Review product changes for impact on regulatory filings worldwide. Research regulatory issues and provides guidance and advice to colleagues. Review product complaints to determine if the events are reportable to regulatory agencies. | 03/31/2025 |
| 1426 | Dexcom San Diego, CA SW Development Engineer 2 Master's Degree in a technical discipline Exp: 0-2 years |
Our R&D team is looking for a Software Engineer with experience with data engineering, modeling and machine learning. In this role, you will design, develop, and deploy new data products leveraging a variety of data sources. You will also drive technical design, development and documentation of cross-functional and multi-platform capabilities. You will work in collaboration with data platform engineers, algorithm developers and clinical experts to focus on key metrics for diabetic patients and clinicians. To be successful in this position you will have experience in modern cloud-based systems (GCP, Terraform, BigQuery), development experience using standard modeling and machine learning libraries, understanding of container based platforms such as kubernetes. An essential part of our design involves utilizing PAAS components. | 03/31/2025 |
| 1427 | Dexcom San Diego, CA Process Development Engineer 2 Master's Degree in a technical discipline Exp: 0-2 years |
We are on the lookout for a top-tier Process Development Engineer 2 who brings a “can do” attitude and a desire for deep technical expertise in equipment, test design, statistics, and data analysis. As an integral part of our Engineering team, you will be instrumental in developing and fine-tuning manufacturing processes for medical devices, ensuring they are robust, efficient, and fully compliant with regulatory standards. Join us and make a significant impact on the future of medical technology! | 03/31/2025 |
| 1428 | Dexcom San Diego, CA Associate Facilities Engineer (HVAC, Plumbing and Electrical) Bachelor’s degree Exp: 0-2 years |
Join the Dexcom San Diego Facilities Engineering team where you will work closely with Manufacturing Operators and Innovators to provide planned and unplanned Facilities systems support. | 03/31/2025 |
| 1429 | Diacarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science Exp: 0-1 years |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 03/31/2025 |
| 1430 | Dimension Inx Chicago, IL Research Associate/Engineer (In Vitro Stem Cells) Bachelor's or Master's degree in Biology, Cell/Molecular Biology, Biochemistry, Biomedical Engineering, Chemical Engineering, Chemistry, or related en Exp: Bachelor's: 1-3 years; Master's: 6 months-1 year |
The Research Associate/Engineer - In Vitro Stem Cells will play a key role in advancing Dimension Inx’s core platform technology and will work closely with the R&D and product development teams to conduct stem cell culture, in vitro testing, and biological assays to support new therapeutic product development to improve patient lives. The ideal candidate is a technically focused scientist or engineer with a background in cell biology, biomedical engineering, or related field, thrives in a rapidly changing, fast-paced environment, and has experience working on multiple and varied projects simultaneously. This position will report directly to a senior R&D team member. This role will contribute to the progression of collaborative early-stage R&D projects, the testing and development of new biomaterial and biological products, as well as various new product development projects. | 03/31/2025 |
| 1431 | Dimension Inx Chicago, IL Research Associate/Engineer (In Vivo & Histology) Bachelor's or Master's degree in Biology, Cell/Molecular Biology, Biochemistry, Biomedical Engineering, Chemical Engineering, Chemistry, or related en Exp: Bachelor's: 1-3 years; Master's: 0-1 years |
The Research Associate/Engineer - In Vivo/Histology will play a key role in advancing Dimension Inx’s core platform technology and will work closely with the R&D and product development teams to execute in vivo experiments, biological assays, and histological analyses to support new therapeutic product development to improve patient lives. The ideal candidate is a technically focused scientist or engineer with a background in cell and tissue engineering, biomaterials, or regenerative medicine, thrives in a rapidly changing, fast-paced environment, and has experience working on multiple and varied projects simultaneously. The position will report directly to a senior R&D team member. This role will contribute to the progression of collaborative early-stage R&D projects, the testing and development of new biomaterial and biological products, as well as various new product development projects. | 03/31/2025 |
| 1432 | Dimension Inx Chicago, IL Project Engineer (Materials) Bachelor's or Master's degree in Materials Science and Engineering, Chemical Engineering, Biomedical Engineering, Chemistry, Mechanical Engineering, o Exp: Bachelor's: 1-3 years; Master's: 0-1 years |
The Project Engineer - Materials will play a key role in advancing Dimension Inx’s core platform technology and will work closely with the R&D and product development teams to design, iterate, test, and produce materials for novel therapeutic products to improve patient lives. The ideal candidate is a technically focused engineer with a background in materials science or biomaterials, and thrives in a rapidly changing, fast-paced environment, and has experience working on multiple and varied projects simultaneously. The Project Engineer will report directly to the Lead Project Engineer. This role will contribute to the progression of collaborative early-stage R&D projects, the testing and development of new biomaterial and biological products, as well as various new product development projects. | 03/31/2025 |
| 1433 | DM Clinical Research Chicago, IL Administrative Research Assistant Bachelor’s degree in a healthcare-related field Exp: 1-2 years |
The Administrative Research Assistant plays a key role in providing administrative support to the clinical research team. This includes managing day-to-day operations, coordinating schedules, handling documentation, and ensuring smooth communication between team members, clients, and other stakeholders. The position requires a high level of organization, attention to detail, and familiarity with clinical research protocols and regulatory requirements. | 03/31/2025 |
| 1434 | DM Clinical Research Houston, TX PBMC Lab Technician Bachelor’s degree Exp: 1-2 years |
A PBMC Laboratory Technician will be responsible for conducting special laboratory procedures for clinical trials performing high complexity laboratory techniques including, but not limited to routine isolation of peripheral blood mononuclear cells (PBMC), or other laboratory procedures, etc., ensuring safety measures are followed by facilitating laboratory operations. | 03/31/2025 |
| 1435 | Eurofins San Diego, CA Asbestos PLM Analyst Bachelor’s degree in microbiology, biology, geology or a closely related science Exp: 1+ years |
The Analyst primarily performs analysis of bulk samples using PLM for asbestos. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and enters laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 03/31/2025 |
| 1436 | Eurofins St. Louis, MO Associate Scientist - Analytical Assay Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related fields Exp: 1-3 years |
The position will be providing analytical support to biotherapeutic process development teams, specifically focusing on large molecules (proteins, polysaccharides, nucleic acids, etc.). Candidates should have familiarity with several of the below laboratory techniques; they should also possess expertise/knowledge with: Ultraviolet and visual light spectroscopy (UV-Vis), Analytical chromatographic separations using HPLCs or UPLCs, SEC-MALS, Small-volume multichannel pipetting skills and plate-based assays | 03/31/2025 |
| 1437 | Edwards Naperville, IL Engr I, Software Quality - Failure Analysis Master's Degree in Engineering or Scientific field Exp: No exp |
Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. | 03/31/2025 |
| 1438 | Edwards Naperville, IL Engineer I, Field Services/Technical Product Support Bachelor's Degree in Electrical, Computer Science, Biomedical, Mechanical, or Reliability Engineering Exp: 1-2 years |
Troubleshooting advanced technical support issues in the field that are escalated by the customer support team. This will include the intake, investigation, documentation, and resolution of complaints and other field issues. | 03/31/2025 |
| 1439 | eGenesis Northwest, IN Quality Control Technician B.S./M.S. in Life Sciences or related field Exp: 0-3 years |
eGenesis is seeking an innovative Quality Control Technician to provide day to day technical support of eGenesis’ environmental monitoring program. In this position you will be responsible for hands on environmental monitoring sampling, testing, reporting and trending of eGenesis’ GMP manufacturing facility (Norwest Indiana). You will ensure activities are executed in a cGMP compliant manner and will work collaboratively on support of our contamination control program. The ideal candidate will be independently motivated, a strong communicator and demonstrate proficiency in regulatory compliance. This position will be an onsite position in Northwest, IN. | 03/31/2025 |
| 1440 | eGenesis Madison, WI Research Associate, Assisted Reproductive Technologies BS/MS degree in animal science, biology, or a related discipline Exp: 1-3 years |
eGenesis is seeking a Research Associate II/Senior Research Associate to join the Process Development team and contribute to projects in andrology, embryology and cell culture. In this role, you will have the opportunity to get hands-on training from experts in these areas. Daily activities include execution of experiments, recording of data into electronic notebooks, and collaborating with other members of the Process Development team. By improving the pig production process, we contribute to the xenotransplantation program of eGenesis. | 03/31/2025 |
| 1441 | Elekta San Jose, CA Associate Medical Device Engineer (Contract) Bachelor's Degree in BioMedical, Mechanical, or equivalent Exp: 6-12 months |
Engineers who are in an early career stage as an individual contributor and are developing their general knowledge and skills. This a contract position. | 03/31/2025 |
| 1442 | Element Biosciences San Diego, CA Senior Manufacturing Technician - Chemistry Bachelor of Science degree in biology, biochemistry, chemistry, molecular biology, or other related life science discipline Exp: 0-2 years |
We are seeking an experienced Senior Manufacturing Technician who will play a pivotal role in supporting the manufacturing and QC of reagent consumables for Element Biosciences. This will include synthesis, purification, and analysis of key intermediates. This is an incredible opportunity for someone who is passionate about making a difference and looking to further their career in the biotech industry. This role will report to our Associate Director, Consumables Manufacturingand will be a San Diego based (on-site)role. | 03/31/2025 |
| 1443 | Elephas Madison, WI Data Scientist Bachelor’s or Master’s degree in Biostatistics, Bioinformatics, Biomedical Engineering, Data Science, Computer Science, or related field Exp: 1-3 years |
Elephas is a Madison, WI based biotechnology start-up company working to build an instrument platform that will inform how clinicians treat cancer patients around the world. We are seeking a highly motivated Data Scientist to join our dynamic team of scientists and engineers developing a platform to predict a cancer patient’s response to immunotherapy. The successful candidate will be motivated to develop analytical, statistical and computational data science methods and deliver data discovery and insights in a fast-paced, collaborative and interdisciplinary environment. | 03/31/2025 |
| 1444 | Veracyte San Diego, CA Histology Associate Bachelor's Degree in life sciences Exp: 1-2 years |
The Histology Associate I primary responsibility is to assist histology with specimen processing in the clinical laboratory. This may include receiving specimens, ensuring accurate entry into the Laboratory Information System (LIS), and /or preparing samples for testing and analysis. The Histology Associate I is knowledgeable with, and is a resource for others within the laboratory, the use of equipment, databases, and software applications. Maintains flexibility regarding work schedule including section assignment. | 03/27/2025 |
| 1445 | Veracyte Austin, TX Specimen Processor Bachelor’s degree Exp: 0-2 years |
The Specimen Processor in this CLIA Laboratory is a critical member of the laboratory team, responsible for receiving, accessioning, and documenting specimens with precision. This role requires accurate data entry, proactive identification, and resolution of sample integrity issues. Flexibility in scheduling, including holidays and variable shifts, is essential to meet operational demands. | 03/27/2025 |
| 1446 | Veracyte San Diego, CA Research Associate, Product Development MS in Genetics, Biochemistry, Molecular Biology or a related scientific field Exp: 1+ years |
Veracyte is seeking an exceptional candidate for a full-time Research Associate in the Product Development team at our San Diego location. The Product Development team at Veracyte is tasked with developing high impact diagnostic assays to address unmet clinical need and improve patient outcomes. This on-site role will be primarily working in the San Diego laboratory supporting the Product Development team in achieving both short- and long-term goals and is a fantastic opportunity to gain hands-on, applied skills within an R&D team at an industry-leading diagnostics company. | 03/27/2025 |
| 1447 | Cabaletta Bio Philadelphia, PA Process Engineering Associate, Person-In-Plant Bachelor’s degree Exp: 1-2 years |
The Process Engineering Associate, Manufacturing Science and Technology (MS&T) is responsible for supporting clinical and commercial manufacturing production at Cabaletta’s cell therapy CDMO. This position will work very closely with manufacturing partners and requires frequent work onsite at manufacturing facility and occasional weekend and overtime work. | 03/27/2025 |
| 1448 | Cambrex Waltham, MA Associate Scientist BS or MS in chemistry Exp: 0-4 years |
Snapdragon Chemistry is currently seeking exceptional candidates for its Associate Scientist or Senior Associate Scientist position in Waltham, MA. A successful candidate will be joining a group of innovative and entrepreneurial scientists, with broad deliverables including the design of synthetic routes amenable to continuous flow processing, the development of reactor systems incorporating cutting-edge flow technology, and delivering intermediates, APIs and high value specialty chemicals to our clients. We are looking for a candidate who has a passion for working in a fast-paced, dynamic environment. The ideal candidate will have a BS or MS in chemistry with experience working in a chemistry research lab. The candidate should have experience in using kinetic analysis and other experimental tools to determine reaction mechanism and experience with typical analytical methods. Experience with the development of reactions in flow is preferred but not required. Candidates must possess strong written and oral communication skills. | 03/27/2025 |
| 1449 | Cambrex Durham, NC Scientist II (ARD) MS Chemistry Exp: 0+ years |
As a Scientist I (QC) in the Cambrex Analytical team, you will support a diverse range of client programs and be an integral team player within a highly cross-trained analytical core team. Execute analytical methods and provide general analytical support, such as release and stability testing of drug substances and drug products. Able to organize routine work independently and to evaluate, troubleshoot and interpret generated data. Demonstrated understanding of method development and qualification / validation principles. Routinely and effectively interacts with clients to discuss data and methods. Works on problems of moderate and sometimes advance scope in which analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. | 03/27/2025 |
| 1450 | Cambrex Charles City, IA Project Engineer BS in Engineering Exp: 1-3 years |
The Project Engineer performs general engineering duties for new installations and equipment, and modification of existing facilities and equipment. These duties are to be carried out with safety, efficiency and quality at the forefront. | 03/27/2025 |
| 1451 | Cambrex Longmont, CO Associate Scientist, Manufacturing BS in chemistry or related field Exp: 0-3+ years |
The Associate Scientist, Manufacturing will work within a team to perform kilogram scale organic synthesis of pharmaceutical drug substance. The Associate Scientist will operate chemical manufacturing equipment and execute detailed written instructions from a batch record under Good Manufacturing Practice (cGMP) conditions. In addition, the Associate Scientist is responsible for maintaining the manufacturing suites for activities by properly setting up, breaking down, operating, and cleaning production equipment for both GMP and non-GMP drug substance manufacturing operations. An Associate Scientist in manufacturing will operate under and develop subject matter expertise in cGMP practices and Good Documentation practices (GDP) within the Quality Management System. | 03/27/2025 |
| 1452 | Cambrex Marlborough, MA Clean Room Analyst - Microbiological Environmental Monitoring Bachelor’s degree or higher in Microbiology or related field Exp: 1 year |
Our Clean Room Services team is looking for both entry level and veteran Environmental Monitoring Analysts that are passionate about leveraging their talents to provide an outstanding customer experience. If you’re interested in receiving excellent training and working as part of a team of experts with opportunities for growth, you’ll be a great fit in our strong company culture. As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 03/27/2025 |
| 1453 | Cambridge Isotope Laboratories Andover, MA Senior Chemist I Bachelor's or Master's degree in Chemistry or a related field Exp: 1-3 years |
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Senior Chemist I based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Senior Chemist I will be responsible for the de novo synthesis, route development, and final product characterization of a wide variety of complex isotopically labeled targets (13C, 15N, 18O, and D isotopes). This role demands the production of high-quality, finished products in accordance with established specifications, while adhering to CIL’s safety and general policies. The Senior Chemist I will operate with a high degree of autonomy, ensuring that production requirements for safety, yield, time, and quality are consistently met. | 03/27/2025 |
| 1454 | Cambridge Isotope Laboratories Andover, MA Chemist, Deuterated Solvents and Reagents BS in Chemistry or related field Exp: 1-2 yeaers |
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Chemist, Deuterated Solvents & Reagents based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Chemist, Deuterated Solvents and Reagents role will support the Solvents and Reagents group, under the supervision of a group leader or supervisor to execute chemical exchanges, enrichment, and purification of isotopically labeled solvents, products and materials utilizing highly detailed SOPs and procedures. They are also responsible for supporting continuous improvement projects on safety, quality, and productivity. | 03/27/2025 |
| 1455 | Capricor Therapeutics San Diego, CA MSAT Training Specialist Bachelor’s degree in a life science discipline (e.g., Biology, Biotechnology) Exp: 1-3 years |
We are looking for a dedicated and detail-oriented Training Specialist to join our team and drive excellence in our GMP manufacturing operations. In this position, you will play a critical role in designing, implementing, and continuously improving training programs for our Cell Therapy Manufacturing Team. You will help ensure that all personnel maintain a high standard of skill, knowledge, and compliance with GMP and regulatory requirements, ultimately supporting the safe and efficient production of our innovative therapies. | 03/27/2025 |
| 1456 | Capricor Therapeutics San Diego, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field. Exp: 1-3 years |
As a Manufacturing Associate, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success. | 03/27/2025 |
| 1457 | Capricor Therapeutics San Diego, CA Process Development Associate 2/3 Master's degree in a scientific discipline (e.g., biology, biotechnology, or related field) Exp: 0-2 years |
The Process Development Associate will play a key role in advancing Capricor’s biomanufacturing efforts by evaluating, improving, and scaling processes for therapeutic production. This position focuses on optimizing product yield, reducing costs, and ensuring scalability—from small experimental batches to large-scale manufacturing—while maintaining quality and efficiency. Reporting to the Process Development Director or Associate Scientist, the associate will collaborate with cross-functional teams to support the production of cell -based therapeutics, troubleshoot challenges, and implement innovative solutions. This role is ideal for a hands-on, detail-oriented professional eager to contribute to cutting-edge biotech advancements. | 03/27/2025 |
| 1458 | Capricor Therapeutics Los Angeles, CA Quality Assurance Associate 1 Bachelor’s Degree Exp: 1+ years |
Capricor is seeking a self-motivated team player with attention to detail, who enjoys organizing, making processes better, and making a difference in patient lives. The successful candidate will serve an essential role in supporting clinical product launch and production. This includes batch record review, deviation investigation, label issuance, and word processing, tracking, issuing, distributing, and archiving companywide GLP / GCP / GMP controlled documentation, training, and facility support systems. Knowledge of standard processes involved in document control and experience in an FDA regulated environment is required. The position will report to the Quality Assurance Supervisor. | 03/27/2025 |
| 1459 | Capstan Medical Santa Cruz, CA Manufacturing Engineer I-II BS or MS in related engineering discipline Exp: 1+ years |
The Manufacturing Engineer will have the exciting opportunity to join a growing team and work on developing and supporting manufacturing processes for our structural heart products. What you’ll do: Develop and support the manufacturing processes for a new heart valve implant, Assist in a transfer from R&D to Manufacturing through Clinical Use, Identify and act upon areas for manufacturing process improvement, Troubleshoot manufacturing issues and collaborate cross-functionally to implement corrective actions, Provide guidance and perform training to technicians and operators for manufacturing processes, Other responsibilities as determined by project need | 03/27/2025 |
| 1460 | Caris Life Sciences Phoenix, AZ Pathologist Associate I Bachelor’s degree in a chemical, biological, clinical or medical laboratory science Exp: 1+ years |
The Pathologist Associate is responsible for supporting and assisting the Pathology and Pathology Operations departments in their daily operations. This position will perform tasks needed to be completed in the day-to-day operation. This position also includes performing the tasks of Macrodissection and Microdissection. | 03/27/2025 |
| 1461 | Caris Life Sciences Phoenix, AZ Development Associate II Bachelor’s or Master's degree in a Molecular Biology, Molecular Genetics, Biochemistry, or related field Exp: 1 year |
The qualified candidate will be working in the Assay Development and Validation Department. The individual will play a critical role in supporting the development, validation, transfer, establishment and successful launch of new molecular assays, instrumentation, and methodologies into the clinical laboratory. Candidate will be responsible for assisting with planning, designing, and performing various laboratory experiments, documentation, reagents receiving, storing and tracking, data analysis, summarization and presentation, transfer of knowledge to other team members and to other departments, training clinical personnel, as well as additional functions fit for the position. Development Associates are expected to contribute both technically and intellectually to optimize quality and efficiency for Caris’ pipeline of development projects. | 03/27/2025 |
| 1462 | Cell Signaling Technology Beverly & Danvers, MA Lab Technician II BS/BA Degree in Chemistry or related science Exp: 1+ year |
The Lab Technician II - Buffer Prep position is primarily responsible for following standard operating procedures, with increasingly limited supervision and also as part of a team, to provide high quality chemical solutions, highly responsive service, and to perform a wide variety of basic laboratory tasks in support of CST's Production, Development, and Research laboratories. | 03/27/2025 |
| 1463 | Cellares Bridgewater, NJ Process Engineer (I, II, III) Bachelor’s or Master’s degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, or a related field Exp: 0-4 years |
We are seeking an innovative and highly motivated Process Engineer on our MSAT team who will contribute significantly to establishing our IDMO Smart Factories. This position is focused on supporting the development and implementation of automated cell therapy manufacturing processes. You will work closely with the Process Engineering Lead and other cross-functional teams to execute, develop, design, optimize, and validate processes to ensure efficient, high-quality, scalable manufacturing solutions. This is a multidisciplinary role & this individual will interface across many parts of the company (with customers, scientists, researchers, and engineers) to develop the best solutions possible. Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company grows. | 03/27/2025 |
| 1464 | Cellares South SF, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 03/27/2025 |
| 1465 | Cellares Bridgewater, NJ Cell Therapy Manufacturing Specialist Bachelor’s Degree Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Specialist to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 03/27/2025 |
| 1466 | Centerline Biomedical Cleveland, OH Quality Engineer Bachelor's Degree in Engineering or related technical field Exp: 1-3+ years |
The Quality Engineer is an Exempt/Full-Time role responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 14971, ISO 13485:2016, MDSAP and FDA 21 CFR Part 820. This role supports supplier quality and monitoring primarily along with complaint/CAPA investigations, operations production and process controls, and product and service quality and the use of statistical techniques and other accepted quality principles. The Quality Engineer will also plan and execute activities concerned with the development, implementation, maintenance, and continuous improvement of Centerline’s quality systems. | 03/27/2025 |
| 1467 | Centrillion Palo Alto, CA Laboratory Technician B.A./B.S in a molecular biology, biochemistry, genetics, or microbiology Exp: 6 months |
We are looking for a Laboratory Technician to join our R&D team in Palo Alto. The role is part of a small group that divides their focus between innovative new projects and product development. The ideal candidate will be extremely organized, familiar with basic laboratory techniques, and excited to learn and grow within the team. Technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. Candidates with knowledge and experience of PCR, library preparation, NGS sequencing or RNA seq will be given preference. | 03/27/2025 |
| 1468 | Charles River Horsham, PA Formulations Technician I Bachelor’ degree (B.S.) Exp: 0-1 years |
Perform routine preparation of vehicles and test article dosage solutions for use in toxicology studies with close supervision. | 03/27/2025 |
| 1469 | Charles River Horsham, PA Research Assistant I – Analytical Chemistry Bachelor’s degree (B.A. / B.S) Exp: 0-2 years |
Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Perform basic laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols and company policies/practices. • Input, print and edit computer entries (e.g., laboratory data). • Prepare materials and data for shipment and archiving. • Receive samples and complete tracking documentation. • Review documentation of functions performed as part of quality control requirements. • Perform study preparation activities. • Maintain clean work areas. • Perform all other related duties as assigned. | 03/27/2025 |
| 1470 | Charles River Malvern, PA Technician I Microbiology Bachelor’s degree (B.A./B.S.) or equivalent in Biology or related discipline Exp: 0-1 years |
Responsible for performing daily laboratory tasks as they relate to Microbiology Testing Services. | 03/27/2025 |
| 1471 | Charles River Rockville, MD QC Associate I – Environmental Monitoring B.S in Biology or related field Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Analyst I will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 03/27/2025 |
| 1472 | Charles River Ashland, OH Technician II, Formulations Bachelor’s degree (B.A./B.S.) Exp: No exp |
A Technician II will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight. We are seeking an experienced Formulations Tech II for our Formulations Team at our Safety Assessment site located in Ashland, OH. | 03/27/2025 |
| 1473 | Charles River Ashland, OH Research Analyst I – Immunology Bachelor’s degree (B.A/B.S.) Exp: 0-2 years |
Perform laboratory tasks by various basic methods. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. We are seeking a Research Analyst 1- for our Immunology team at our Safety Assessment site located in Ashland, OH. | 03/27/2025 |
| 1474 | Charles River Spencerville, OH In Vivo Technician I Bachelor’s degree (B.A./B.S.) in a biological science Exp: No exp |
A Technician I is in training to perform and become proficient in on-boarding tasks, procedures, and cooperating in a team environment. The technician is learning basic tasks required to conduct a study, which may include collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. The technician is working under close supervision to gain proficiency | 03/27/2025 |
| 1475 | ChemGenes Wilmington, MA Senior Research Support Associate B.S. degree in Biochemistry, Biology or related field Exp: 0-2 years |
Manufacture of synthetic DNA & RNA compounds. Assist with experiments supporting research in the synthesis of single-cell-barcoded beads, quality control of the synthesized beads, and performing experiments that include basic molecular biology techniques to sequencing experiments to validate and troubleshoot synthesis of DNA oligos to beads. Provide comprehensive technical support for scientists in the company; executing and optimizing ongoing experiments, analyzing results and designing follow-up experiments based on the results, and presenting findings and insights at group meetings. Evaluating research methods, procedures and techniques based on established objectives, conceiving and designing basic experimental protocols to ensure project completion in a timely fashion; recording and organizing data generated from the experiments in clear, concise, and assessable format; perform basic coding and statistical analyses; processing of in-vitro and in-vivo RNA for preparation of RNA-seq libraries for sequencing in Illumina platforms (Mi-Seq including Hi-seq and Next-seq). Experienced in techniques including but not limited to: running agarose gel, polyacrylamide gel electrophoresis, reverse transcription, quantitative PCR, fluorescent microscopy, flow cytometry; maintaining inventories of lab stocks. | 03/27/2025 |
| 1476 | ChemPacific Baltimore, MD Chemist, Deuterated Solvents and Reagents Master’s degree in Chemistry or Organic Chemistry Exp: 1 year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 03/27/2025 |
| 1477 | Cipla Central Islip, NY QC Chemist III Master of Science Degree Chemistry, Pharmaceutical Sciences, or related field Exp: 1 year |
Perform analytical testing for Raw Materials, Finished and In-Process of Drug Substances and Products like Related Compounds, Assay, Content Uniformity, Dissolution, Blend Uniformity, Karl Fischer Titration, and other related Physical testing for the methods using instruments HPLC, UV/VIS, Dissolution (USP-I, II & III) and FTIR. Execute Method validations of Drug Substance and Drug Products including Related Compounds, Assay, Dissolution, Content Uniformity, Blend Uniformity as per ICH guidelines/USP /FDA requirements. Collaborative team player with excellent communication skills working in a highly dynamic, cross disciplinary environment. Develop efficient and selective analytical procedures and draft/review laboratory SOPâ_x0080__x0099_s. Identify discrepancies, initiate, and investigate OOS/OOT results. Perform timely and accurate peer review of analytical test results report/document in notebooks. Maintain QC lab related systems to ensure compliance with industry standards. | 03/27/2025 |
| 1478 | Cipla Central Islip, NY QC Chemist II (DPI), Level 1 Bachelor's or Masters degree (BS or BA), physical sciences Exp: 0-3 years |
The job of the "Chemist" is simple described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three. Generally, modifier designation with respect to experience for Chemist are as follows. However, combination of education, training, and special skills will determine the assignment of Level to a specific individual: | 03/27/2025 |
| 1479 | Cirtec Medical Lowell, MA Manufacturing Engineer I (Photolithography) Bachelor’s degree in engineering (STEM) Exp: 1-2 years |
This position is primarily responsible for developing and implementing robust cost-effective manufacturing processes and methods in accordance with product specifications within thin film fabrications. This position recommends and implements improvements to sustained production processes, methods and controls; as well as coordinates the launch of new products into pilot production. | 03/27/2025 |
| 1480 | Cleveland Diagnostics Cleveland, OH Associate Scientist- IVD Test Development Bachelor’s degree in Biology, Biochemistry, Molecular Biology, Biomedical Engineering, or a related field Exp: 1-4 years |
We are seeking a highly motivated Associate Scientist with experience or interest in in vitro diagnostic (IVD) assay development to join our dynamic team. The successful candidate will perform laboratory work, data analysis, under the guidance of a supervisor. This role requires hands-on execution of experiments, routine lab maintenance, and meticulous documentation to support product development, validation, and verification initiatives. The position involves handling human biological specimens, including blood, plasma, urine, and other bodily fluids, in compliance with all safety regulations and company policies. | 03/27/2025 |
| 1481 | Coastar Therapeutics San Diego, CA Research Associate II M.S. or B.S. degree Exp: 1-3 years |
Coastar Therapeutics is currently seeking a talented and highly motivated research associate with molecular biology background to join the multidisciplinary R&D team. The candidate will be responsible for designing and executing experiments in support of the biological membrane coated virus development. The candidate will also be involved in developing and validating collaborating projects to support Coastar’s fast-growing preclinical pipelines. The successful candidate must demonstrate broad and in-depth knowledge of molecular biology techniques. This is a full-time position reporting to the CSO and is located at our corporate headquarter in San Diego. | 03/27/2025 |
| 1482 | Color Health Burlingame, CA Clinical Lab & Fulfillment Associate (Temp Contract) Bachelor's degree in a relevant scientific field Exp: 1 year |
Color Health is revolutionizing cancer care with the nation’s first Virtual Cancer Clinic, delivering high-quality, physician-led multidisciplinary care across all 50 states. Our innovative, guideline-based approach spans cancer screening, risk assessment, prevention, diagnosis, treatment support, and survivorship. In addition to personalized direct medical care, our services include cancer genetics risk assessment, nutrition, mental health support and at-home cancer screening diagnostics. Using technology-driven, patient-centric solutions, Color is transforming how employers, unions, health plans, and governments address cancer. Color’s goal is to close critical cancer care gaps, improve cancer outcomes, and guide patients with empathy through their healthcare journeys. Color Health is seeking a Clinical Lab & Fulfillment Associate to support daily operations in our high-complexity CLIA-certified laboratory. This role will involve assisting with clinical testing, laboratory maintenance, and fulfillment operations to ensure seamless processing of biological specimens and timely distribution of testing materials. | 03/27/2025 |
| 1483 | Confluent Medical Technologies Laguna Niguel, CA Process Development Engineer I BS degree in engineering Exp: 0-3 years |
Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers. | 03/27/2025 |
| 1484 | BD Carol Stream, IL Quality Control Technician Bachelor's degree in related field Exp: 1 year |
The Quality Control Tech 2 works in the Quality Control department and performs general quality control quality assurance testing and review activities in accordance with current Good Manufacturing Practices (cGMP), company policy and safety regulations. | 03/16/2025 |
| 1485 | Bifrost Biosystems Berkeley, CA Mechanical Engineer BS or MS in Mechanical Engineering or a related field Exp: 0-4 years |
Are you passionate about pushing the limits of technology to advance our understanding of the life sciences? So are we! We’re looking for a highly motivated and experienced Mechanical Engineer to join a fast-paced start-up developing tools that will transform functional cell biology research. The ideal candidate will have strong engineering and problem-solving skills, a solid grasp of mechanical design fundamentals and some exposure to optical systems, microscopy and bio-engineering or biology. As Mechanical Engineer, you will be part of a small team designing, developing, specifying and testing Bifrost’s hardware products. Additionally, you will play a role in product definition, development and verification testing. | 03/16/2025 |
| 1486 | Abbott Temecula, CA Manufacturing Engineer Bachelors Degree Exp: 0-3 years |
Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents | 03/16/2025 |
| 1487 | Abbott Scottsdale, AZ Manufacturing Engineer I Bachelors Degree Exp: 0-3 years |
This position supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. This individual will work with supervisors, engineers, technicians, and operators to address problems and opportunities identified on manufacturing lines. He or she will be accountable for quality, safety, product output and yield initiatives, as well as providing line support on a daily basis. | 03/16/2025 |
| 1488 | Abbott Sylmar, CA Manufacturing Engineer I Bachelors Degree Exp: 0-3 years |
This position supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. This individual will work with supervisors, engineers, technicians, and operators to address problems and opportunities identified on manufacturing lines. He or she will be accountable for quality, safety, product output and yield initiatives, as well as providing line support on a daily basis. | 03/16/2025 |
| 1489 | Abbott Liberty, SC Manufacturing Engineer I Bachelors Degree Exp: 0-3 years |
This position supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. This individual will work with supervisors, engineers, technicians, and operators to address problems and opportunities identified on manufacturing lines. He or she will be accountable for quality, safety, product output and yield initiatives, as well as providing line support on a daily basis. | 03/16/2025 |
| 1490 | Abbott Minnetonka, MN Manufacturing Engineer I Bachelors Degree Exp: 0-3 years |
This position supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. This individual will work with supervisors, engineers, technicians, and operators to address problems and opportunities identified on manufacturing lines. He or she will be accountable for quality, safety, product output and yield initiatives, as well as providing line support on a daily basis. | 03/16/2025 |
| 1491 | Abbott Scottsdale, AZ Process Engineer Bachelors Degree Exp: 0-2 years |
This position works supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Process Engineer performs analyses to develop design specifications and performance requirements. Provides technical information concerning manufacturing or processing techniques, materials, properties and process (advantages/limitations) engineering planning. Selects techniques to solve problems and make sound design recommendations. | 03/16/2025 |
| 1492 | Abbott Sylmar, CA Process Engineer Bachelors Degree Exp: 0-2 years |
This position works supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Process Engineer performs analyses to develop design specifications and performance requirements. Provides technical information concerning manufacturing or processing techniques, materials, properties and process (advantages/limitations) engineering planning. Selects techniques to solve problems and make sound design recommendations. | 03/16/2025 |
| 1493 | Biocytogen Boston, MA In vivo Pharmacology Research Associate Bachelor’s or Master’s degree Exp: 1-5 years |
Biocytogen is a comprehensive research and discovery service provider for biotech and pharmaceutical industry and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, antibody discovery, and animal supplies, with current focus on immuno-oncology and oncology. We are looking for a highly motivated research associate with the ability to work both independently and in a collaborative manner. Biocytogen is a fast-growing company and has an abundance of opportunities available for you to grow your career. | 03/16/2025 |
| 1494 | BioMérieux Salt Lake City, UT Research Associate I Bachelor's degree in related field Exp: 6 months |
The Research Associate I (RA I) work to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and bioMérieux. A Research Associate I may receive general or detailed instruction and direct supervision on general work, new procedures, and assignments. | 03/16/2025 |
| 1495 | BioMérieux Philadelphia, PA Quality Engineer Masters’ degree in a life science or related field Exp: 1+ years |
The QA Engineer is responsible for supporting and facilitating the quality management system of the bioMérieux Philadelphia site. Under the guidance of the Quality Manager, the QA Engineer will work collaboratively with other departments including manufacturing, R&D, and purchasing to ensure compliance to the quality management system. Additionally, this position will assist in executing various site-wide quality projects and initiatives. The incumbent is responsible for monitoring site activities to ensure appropriate quality reporting and compliance to ISO9001:2015 standards. The QA Engineer will have a specific focus on supplier quality management, risk analysis of site processes, continuous process improvement, and sustaining quality management system activities. | 03/16/2025 |
| 1496 | BioMérieux Hazelwood, MO Final QC Microbiology Lab Tech Bachelor’s degree Exp: 0 years |
Using good aseptic lab practices, is responsible for supporting performance testing and physical inspections of finished good lots as well as internal use only lots through set up of VITEK2 cards, to completion. This position performs environmental testing and ensures proper documentation according to cGMP’s and current procedures, to completion. Performs all duties using safety conscious practices. Technician will uphold the lab attendance policy. | 03/16/2025 |
| 1497 | BioMérieux Philadelphia, PA PCR Technician 1 Bachelor’s degree in Biology or related field Exp: 0-2 years |
The PCR Specialist 1 is responsible for the formulation of highly complex PCR products and sub-solutions within the required timeframes and production schedules, in compliance with established Safety and Quality standards. They will be responsible for the proper handling and accurate pipetting of numerous different raw materials, combining 5-15 components into a final chemical formulation. Additionally, they will be responsible for the proper dispensing and labeling into final, customer facing formats. | 03/16/2025 |
| 1498 | Biogen Research Triangle Park, NC Manufacturing Associate - Biologics Bachelor’s Degree (STEM preferred) Exp: Entry Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 03/16/2025 |
| 1499 | Biogen Research Triangle Park, NC Manufacturing Associate II - Visual Inspection Bachelor’s Degree (STEM preferred) Exp: 6 months |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. | 03/16/2025 |
| 1500 | BioMarin Novato, CA Lead, Manufacturing (Day Shift) BA/BS Exp: 1-2 years |
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These individuals build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. | 03/16/2025 |
| 1501 | BioMarin Novato, CA Lead, Manufacturing (Grave Shift) BA/BS Exp: 1-2 years |
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These individuals build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. | 03/16/2025 |
| 1502 | BioMarin Novato, CA Analyst, QC I Bachelor of Science degree Exp: 0-3 years |
Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with agreed upon best practices. Execute microbiological and/or analytical methods to facilitate in-process testing under applicable cGMP guidelines, as well as contribute to the prompt reporting of results to meet the required timetables of internal customers. Perform environmental monitoring sampling and testing of facilities, equipment, and utilities. Evaluate completed assay validity, calculate and summarize results, analyze data per expected or specification ranges. Assist with the compilation and verification of trend analysis reports. Perform and collaborate with co-workers to appropriately share general housekeeping activity assignments, and ensure systems for laboratory maintenance are adequate for creating a consistent state of inspection readiness. Assist with monitoring and the control of laboratory supply and critical reagent inventories. Perform growth promotion of media and microbial identification testing. Qualify as trainer for specified methods, provide training to less experienced staff. Provide on call coverage to support oversight of QC laboratory equipment functionality. Exhibit proactive communication upon occurrence of compliance risks and deviations from laboratory procedures, perform initiation of investigation records within required timeframes. Provide input or assay support to the progression of test method validation, investigations, technical studies, and method transfer protocols. Attend team huddles and department meetings, generate ideas for laboratory infrastructure improvements and method optimization. Perform other responsibilities as deemed necessary. | 03/16/2025 |
| 1503 | BioMarin Novato, CA Research Associate 2, Drug Product Development DPDT MS in physical/Chemical/Biological/Life Science Exp: 0-2 years |
The Research Associate 2 role will support the team by generating high quality data while executing both routine testing and more complex, exploratory research projects. In addition, the candidate is expected to lead certain aspects of projects independently including experimental design, execution, interpretation of results, drafting of technical documents, and communication of data to stakeholders through oral presentations | 03/16/2025 |
| 1504 | Bionova Fremont, CA Sr. Manufacturing Associate BS in Life Sciences, or related discipline Exp: 0-1 years |
The Senior Manufacturing Associate will actively contribute to the manufacturing and technology transfer projects at the Bionova Scientific Fremont location. As part of the Purification/Manufacturing group, you will have opportunities to work on a wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into the GMP manufacturing facility. The role will provide hands-on execution of complex experiments in a team setting. The role will support GMP readiness and manufacturing activities. The scope of responsibilities may include but are not limited to Document writing (SOPs, Equipment URSs, etc.), equipment validation execution support and single-use assembly design. | 03/16/2025 |
| 1505 | Bio-Rad Woodinville, WA Quality Engineer I Bachelor’s degree in a related scientific discipline Exp: 0-2+ years |
Join Bio-Rad as our Quality Engineer and work in our Woodinville, WA site! Working in this Quality Assurance role, you will attend cross functional Daily Management meetings and represent Quality Assurance to address blocking issues and implement counter measures. You will manage the Material Review Board and ensure thorough data-driven documentation of non-conformities and risk based determination of CAPA. You will review data for trends, manage corrections and corrective action and support Global Supply Chain and business partners as requested. | 03/16/2025 |
| 1506 | Bio-Techne Minneapolis, MN Research Associate B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Performing routine quality control testing of stem cell products using protocol-defined assays to demonstrate their activity. The assays include culturing and handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation and workflow is required. Other duties include instrumentation maintenance, reagent preparation and routine lab support for QC antibody testing using western blot, simple wes and immunohistochemistry. | 03/16/2025 |
| 1507 | Bio-Techne Minneapolis, MN Research Associate - GMP Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 03/16/2025 |
| 1508 | Bio-Techne Minneapolis, MN Quality Assurance Specialist Bachelor’s degree in Biology related disciplines Exp: 0-5 years |
The responsibilities of this position are label design and optimization, to perform internal audits, and to engage and support other Quality Assurance activities, including but not limited to, Supplier Management, Training Management, and Document Control. Perform additional duties as assigned. | 03/16/2025 |
| 1509 | Bio-Techne Minneapolis, MN Advanced Manufacturing Tech Bachelors science degree Exp: 1+ years |
The responsibilities of an Advanced Manufacturing Technician is to assist in the process of formulating buffers, diluents, and other components of Bio-techne’s best in class immunoassay products. Daily work may include recording data, operating equipment, product formulation and plate coating. Collaboration with other groups is also part of our work. Employees must have the ability to work independently and as a part of a team environment. Additionally, able to lift or move >50 lbs. routinely. | 03/16/2025 |
| 1510 | PSC Biotech Remote, Validation Engineer Bachelor's degree in related engineering discipline. Exp: 0-1 years |
This position will support system validation and product release processes, ensuring compliance with industry standards and regulatory requirements. You will play a key role in contributing to the development and improvement of validation procedures and driving overall product excellence. This is an entry-level, remote position. Successful candidates have a bachelor’s degree within an engineering discipline, a passion for technology, and exposure to system/software testing in the life science industry. | 03/16/2025 |
| 1511 | PSC Biotech York, PA Metrology Technician I Bachelor's degree in engineering or related technical field Exp: 0-1 years |
We are hiring an entry to junior level Metrology Technician responsible for conducting routine calibration tasks in alignment with established protocols and regulatory mandates. The position adeptly handles troubleshooting and equipment repair as needed, while ensuring the steadfast adherence to quality system compliance standards. | 03/16/2025 |
| 1512 | Bora Pharmaceuticals Camden, MA Analyst I, QC Analytical-2nd Shift B.S. in Chemistry or related field Exp: 0-2 years |
Perform analytical testing per cGMP in support of raw material, in-process, final product, stability. Typical hours are 10:00 pm – 6:30 am, Monday through Friday. Hours may vary to meet business and training needs. | 03/16/2025 |
| 1513 | Bora Pharmaceuticals Camden, MA Analyst II, QC Microbiology-1st Shift MS in Microbiology/Biology or related field Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Bora Pharmaceuticals Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. | 03/16/2025 |
| 1514 | Bora Pharmaceuticals Camden, MA Analyst I, QC Microbiology-1st Shift BS in Microbiology/Biology or related field. Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. | 03/16/2025 |
| 1515 | Bora Pharmaceuticals Camden, MA Analyst I, QC Microbiology-2nd Shift BS in Microbiology/Biology or related field. Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. This position supports our 2nd-shift, working 2pm-10:30m, Monday through Friday. | 03/16/2025 |
| 1516 | BIB Southborough, MA Research Associate, Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields Exp: 1+ years |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision at BIB. | 03/16/2025 |
| 1517 | Boston Scientific Arden Hills, MN R&D Engineer II - Electrophysiology MS in Mechanical or Biomedical Engineering Exp: 1+ years |
The engineer role will be a key team member in providing mechanical engineering support in the creation and development of new electrophysiology ablation catheter technologies. As R&D Engineer II, you will support new product development team solutions to multi-faceted customer issues. You will be a part of a high-performance team responsible for the design, implementation, and test of disposable medical devices within our electrophysiology pulsed field ablation single use device portfolio. This critical role will be a part of best-in-class development practices and rigorous, holistic product design in coordination with internal and external partners. | 03/16/2025 |
| 1518 | Boston Scientific Maple Grove, MN Quality Engineer II - Nitinol MS in engineering Exp: 1+ years |
The Quality Engineer II will be a key member of the Nitinol Shape Memory team supporting the self-expanding component product lines. This role will partner with representatives from the Manufacturing Engineering and Production functions. The person in this role will take the lead in addressing quality issues in a dynamic production environment. The ideal candidate will be comfortable interfacing with downstream internal customers and providing quality leadership to a production team running across 4 shifts. | 03/16/2025 |
| 1519 | Boston Scientific Maple Grove, MN R&D Sustaining Engineer II Master’s degree in Mechanical Engineering, Biomedical Engineering, or related field. Exp: 1 year |
As a R&D Engineer II, you will support commercial product improvement and supply continuity through design and material changes, product expansions, and complex problem solving. This role involves working collaboratively with cross-functional teams to ensure product designs meet the highest quality and regulatory standards. | 03/16/2025 |
| 1520 | Boston Gene Waltham, MA Laboratory Technician, Biospeciman Services Bachelor’s degree in Biological or Life Sciences Exp: 1 year |
The Laboratory Technologist will be responsible for pre-analytical accessioning, processing, and maintaining inventory of clinical blood samples in accordance with established laboratory procedures. This role ensures the integrity of patient samples, supports downstream users in clinical and research operations, and maintains compliance with laboratory quality and regulatory standards. | 03/16/2025 |
| 1521 | Bristol Myers Squibb Devens, MA Senior QC Microbiology Associate, Lab Operations BS/BA in?Biological, Chemical/Life Sciences Exp: 1-2 years |
To perform QC testing in support of bulk drug substance manufacturing using defined methods in a GMP-compliant laboratory. Ensures test results are accurately recorded, and abnormal data or equipment/instrument malfunctions are properly reported and escalated to management | 03/16/2025 |
| 1522 | BWX Technologies Erwin, TN Engineer 2 -- Fuel Dev & Variability Reduction MS. Degree -- Engineering. Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 03/16/2025 |
| 1523 | BWX Technologies Barberton, OH Metallurgical Engineer Bachelor or Master of Science Degree in Metallurgical Engineering, Materials Science & Engineering or Welding Engineering Exp: 1 year |
Provide technical leadership and utilize a background in materials for broad metallurgical support in a project team environment. Candidate will operate metallographic equipment for investigative purposes and communicate closely with others. Prepare, analyze and generate reports for the acceptance of metallographic specimens, primarily welded assemblies, but also includes determination of intergranular attack (IGA), plating thickness, EDM/laser recast layers, grain size, and general microstructural characterization to other specifications and in support of investigations. The candidate will be expected to have the ability to support or lead material-related investigations, develop laboratory best practices/standard procedures and manage metallurgical supply inventories. The ability to lead technical projects/investigations, manage documentation and time management skills are crucial. Familiarity with materials processing (i.e. melting, forging, heat treating, casting, welding, etc.), mechanical testing, metallography, EDM, plating, corrosion, and nuclear-grade materials is strongly desired. | 03/16/2025 |
| 1524 | Shimadzu Central Islip, NY Field Service Technician Associates EE or Bachelors Chem Exp: 1 yr |
Provide daily repair and maintenance support for assigned products; Conduct in-house bench repairs as needed while primarily handling field service calls with limited supervision; Travel within the local region (including day and overnight trips) to support customer needs; Offer technical support via phone to customers and field personnel regarding repairs, maintenance and installations. | 03/13/25 |
| 1525 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone with expertise in classifying diseases/conditions by medical specialty. Contract work on a task basis. Must be able to accept payment by PayPal or Venmo. Send us a message through the contact form if interested. | 03/12/2025 |
| 1526 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Small Scale Synthesis B.S. Chemistry or Biochemistry degree Exp: 0-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Scientist to join the Discovery Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, purification, analytical chemistry, and contributing to specific program goals. The Associate Scientist will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 03/10/2025 |
| 1527 | Arthrex Naples, FL Research Operations Specialist Bachelor’s or Master's degree Exp: 1 year |
Manages with autonomy and independent judgement the daily activities of the Department of Orthopedic Research that supports critical operations and functions. Responsible for departmental strategic development and surgeon collaborations. Spearhead key inter- and intra-departmental initiatives. | 03/10/2025 |
| 1528 | Artivion Austin, TX Associate Regultory Affairs Specialist Bachelor's degree in relevant science Exp: 0-2 years |
The Associate Regulatory Affairs (RA) Specialist is responsible for assessment of device and tissue product changes for regulatory implications and for performing regulatory activities in support of implementing these device changes (e.g., labeling and quality system implementation). The Associate RA Specialist is also responsible for supporting activities related to PMA annual reports, Canadian license renewals and maintaining required facility and state licensing/registrations. Additionally, the Associate RA Specialist will provide regulatory labeling support to ensure labeling compliance. The Associate RA Specialist will work independently with management oversight. | 03/10/2025 |
| 1529 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst I B.S. degree in a relevant scientific discipline Exp: 0-2+ years |
Performs chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with current Good Manufacturing Practices, Associates of Cape Cod Standard Operating Procedures, compliance guidelines of the FDA and other regulatory bodies, and approved license requirements. Learns and executes defined QC tasks efficiently and consistently. Results are compared to specifications and documented in a timely manner. Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 03/10/2025 |
| 1530 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst II M.S. degree preferred in a relevant scientific discipline Exp: 0-2+ years |
Performs chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with current Good Manufacturing Practices, Associates of Cape Cod Standard Operating Procedures, compliance guidelines of the FDA and other regulatory bodies, and approved license requirements. Results are compared to specifications and documented. Analyst has mastered most or all of the fundamental quality control concepts as well as some specialized technologies and receives minimal supervision on routine assignments. Analyzes and interprets test results independently and contributes to design of new studies in consultation with Supervisor. May provide guidance and training to more junior staff members. | 03/10/2025 |
| 1531 | AstraZeneca Mount Vernon, IN PET Formulation - Process Engineer Bachelor’s degree required, preferably in Science, Chemical Engineering, or other related technical discipline Exp: 0-1 years |
Are you ready to break new ground and leave a collective legacy? As a PET Formulation - Process Engineer, you will provide technical support for process manufacturing, investigating and correcting process-related problems and deviations from standards. This role offers the opportunity to play a pivotal part in evolving our Supply Chain, reimagining how we do things, and creating a lasting impact. | 03/10/2025 |
| 1532 | AstraZeneca Frederick, MD Quality Control Analyst Bachelor’s degree required, preferably in Science, Chemical Engineering, or other related technical discipline Exp: 0-5 years |
As a Quality Control Analyst, you will be responsible for conducting raw materials, in process, finished product, and stability testing according to standard operating procedures. You will complete appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms. You will also identify and troubleshoot equipment problems, enter data evaluated for compliance to specifications and report abnormalities. You will own minor deviations and simple change control and CAPA records. You will also support preparation of validation protocols, execute experiments, and provide data for validation reports. | 03/10/2025 |
| 1533 | AstraZeneca Waltham, MA Scientist, Oncology Bioscience MS in Biology, Oncology, Biochemistry, Pharmacology, Immunology or a related field Exp: 1+ years |
Would you like to apply your expertise to impact drug development in a company that follows the science and turns ideas into life-changing medicines? Then employment at AstraZeneca might be the right choice for you! We are seeking a highly motivated Scientist in Oncology Targeted Discovery with strong scientific and technical expertise in oncology research and a track record of scientific excellence to join our team in Waltham, MA USA. As a Scientist in our Oncology R&D department, you will be a key member of a team focused on supporting oncology projects through the drug discovery and development process. You will bring your theoretical and practical expertise in cancer biology to establish assay systems and deliver datasets that will have a direct impact on targeted therapeutics. | 03/10/2025 |
| 1534 | Bio-Techne Minneapolis, MN Research Associate B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Performing routine quality control testing of stem cell products using protocol-defined assays to demonstrate their activity. The assays include culturing and handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation and workflow is required. Other duties include instrumentation maintenance, reagent preparation and routine lab support for QC antibody testing using western blot, simple wes and immunohistochemistry. | 03/10/2025 |
| 1535 | Bio-Techne Minneapolis, MN Research Associate - GMP Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 03/10/2025 |
| 1536 | Bio-Techne Minneapolis, MN Quality Assurance Specialist Bachelor’s degree in Biology related disciplines Exp: 0-5 years |
The responsibilities of this position are label design and optimization, to perform internal audits, and to engage and support other Quality Assurance activities, including but not limited to, Supplier Management, Training Management, and Document Control. Perform additional duties as assigned. | 03/10/2025 |
| 1537 | Bio-Techne Minneapolis, MN Scientific Support Specialist Bachelor’s degree in laboratory science or equivalent Exp: 0-2 years |
Provides high level technical support to customers on use of hematology products. Answers and documents incoming technical inquiries and complaints by phone and email on product techniques, procedures and troubleshooting. Communicates to obtain all pertinent information relating to the inquiry. Provides adequate information to problem solve or to assist in the resolution of the issue. Documents information and recurring technical issues to support product quality programs and product development. Works on complex problems of diverse nature where analysis requires in-depth evaluation of various factors. Supports the Marketing and Sales Departments. Provides guidance and recommendations on products based on customer needs and utilizes customer interactions to improve business opportunities. Collaborate with cross-functional teams for root cause analysis. Helps to identify gaps and collaborates to devise and implement process improvements. Assure a high level of quality and accuracy in the processing of customer QC data. Provide QC program support for OEMs, International Distributors and end-user customers. Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job. | 03/10/2025 |
| 1538 | Avance Biosciences Houston, TX Laboratory Associate II Bachelor’s degree in biological sciences Exp: 1 year |
Carry out Molecular Biology, Microbiology, Protein experiments following established SOPs and/or guidance of laboratory management. Perform DNA/RNA extraction, quantification, and gel QC. Perform PCR setup for qualitative and quantitative analysis. Report experimental results to project managers in a timely manner. Follow established quality management policies and GLP and GMP practices. | 03/10/2025 |
| 1539 | Avanos Medical Alpharetta, GA R&D Professional I Bachelor of Science in Biomedical Engineering or Mechanical Engineering Exp: 0-2 years |
The Research and Innovation (R&I) department will be focused on supporting efforts to grow the Digestive Health Enteral Feeding medical device business. This role requires a professional with entry level experience in Research and Development or New Product Development to deliver on the product development roadmap growing Avanos’ enteral feeding business. This candidate must support technical teams for design, development and implementation of changes and improvements to existing products within Avanos’ Digestive Health Business. | 03/10/2025 |
| 1540 | Avantor Sciences Irving, TX Project Engineer 1 Bachelor’s degree in Mechanical, Electrical, or Chemical Engineering Exp: 1-3 years |
The Project Manager will own project assignments from concept to closure. This will include preparatory documentation, stakeholder engagement, Scope of Work creation, cost estimation, schedule creation, solicitation of funding approvals, procurement activities, construction management, equipment qualification and validation activities, all in a ISO9000, FDA, AS9100, cGMP, ITAR environment. Other activities may be required or assigned depending on the specific project needs. Non-project-related work may include departmental documentation, participation in various initiatives as a team member or Subject Matter Expert, or collaboration with other departments and sites. | 03/10/2025 |
| 1541 | Avid Bioservices Tustin, CA Manufacturing Associate Support Bachelor’s degree with an emphasis in biology or chemistry highly preferred. Exp: 1+ years |
The Manufacturing Associate Support provides support for: Production Operations and multiple aspects of cGMP contract cell culture manufacturing in strict compliance with cGMP, under Standard Operating Procedures in a multi-product manufacturing facility, including, but not limited to production, documentation, writing reports, requesting and purchasing materials, and scheduling equipment services and calibrations. The Manufacturing Associate will play an integral role in ensuring the production and on-time release of quality products. The Manufacturing Associate will conduct themselves in a manner representing the core values (Integrity, Adaptability, Innovation, Teamwork, and Passion) of the company with the common purpose of improving patients’ lives by consistently delivering high-quality biopharmaceutical products. | 03/10/2025 |
| 1542 | Avid Bioservices Tustin, CA Manufacturing Associate, Downstream Bachelor’s degree with a preference for biology or chemistry emphasis. Exp: 1-2+ years |
Join our dynamic team as a Manufacturing Associate, Downstream! In this role, you'll be a crucial part of our multi-product manufacturing facility, working in strict compliance with cGMP and Standard Operating Procedures. Your responsibilities will encompass various tasks, including production, meticulous documentation, report writing, materials procurement, and equipment scheduling. You'll be instrumental in ensuring the timely production and release of top-quality products. At our company, we value core principles such as Integrity, Adaptability, Innovation, Teamwork, and Passion, all united by a shared mission to enhance patients' lives through the consistent delivery of high-quality biopharmaceuticals. If you're ready to make a meaningful impact, apply now and be part of our journey! | 03/10/2025 |
| 1543 | Avid Bioservices Tustin, CA Research Associate, Process Development - Downstream B.S. degree in a Biological Science. Exp: 1-2 years |
The Research Associate, Process Development Downstream will provide laboratory support for Process Development by assisting in the downstream process and/or method development. The Research Associate may be assigned various tasks within the department and outside the department as needed. | 03/10/2025 |
| 1544 | Avid Bioservices Tustin, CA Research Associate, Process Development Upstream B.S. degree in a Biological Science. Exp: 1-2 years |
The Research Associate in Process Development - Upstream will develop and optimize scalable cell culture processes and contribute to transferring the process to Avid Manufacturing. In addition, the Research Associate will maintain production equipment and will research and implement new methods and technologies to enhance process operations. | 03/10/2025 |
| 1545 | Avid Bioservices Tustin, CA Associate Specialist, Quality Assurance B.A. or B.S. degree (preferably in Life Science). Exp: 1+ years |
As an Associate Specialist, Quality Assurance, you will be a critical part of ensuring top-notch quality for our products and services. You will be responsible for various administrative tasks associated with Avid's electronic document management and training systems, issuing, and reconciling equipment logbooks and laboratory notebooks, and providing both formal and informal training to coworkers on relevant processes such as quality systems, training, and GMPs. | 03/10/2025 |
| 1546 | Axogen Vandalia, OH Quality Analyst Bachelor’s Degree in a Life Science discipline, engineering, or in a related field Exp: 0-2 years |
The Quality Analyst I performs quality control (QC) inspection and disposition of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen’s Quality System. The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable FDA, state OSHA, and ISO regs and standards. Employees within this role will perform a variety of tasks under limited supervision. | 03/10/2025 |
| 1547 | B. Braun Medical Daytona Beach, FL QC Lab Tech II-Microbiology Bachelor's degree in relevant science Exp: 1-2 years |
Performs a variety of quality control tests on products at various stages of the production process to ensure compliance with quality and reliability standards. Records statistical data. Analyzes data and writes summaries to validate or show deviations from existing standards. Recommends modifications to existing or suggests new, standards, methods and procedures. | 03/10/2025 |
| 1548 | BA Sciences Salem, NH Analytical Chemist I Bachelor’s degree in Chemistry or a related science discipline Exp: 0-2 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 03/10/2025 |
| 1549 | BA Sciences Salem, NH Microbiologist QC I BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 03/10/2025 |
| 1550 | BA Sciences Salem, NH Microbiologist I – Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and BA Sciences. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 03/10/2025 |
| 1551 | Bachem Vista, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 03/10/2025 |
| 1552 | Bachem Torrance, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 03/10/2025 |
| 1553 | Balt Irvine, CA Manufacturing Engineer Bachelor’s degree in engineering or related field Exp: 1 year |
This fast-paced position will be responsible for the support and continuously improve current manufacturing process, through technical and process innovation for the manufacture of neurovascular medical devices that save patient lives. | 03/10/2025 |
| 1554 | Baxter Medina, NY Manufacturing Engineer Bachelor’s degree in engineering Exp: 1-3 years |
This description outlines the employment prerequisites and job responsibilities for the position of Manufacturing Engineer within the Continuous Improvement Team. Provide support in the execution of the site’s operational optimization and quality improvement projects to achieve Medina Plant goals and objectives. Drive/support various quality improvement, business continuity/expansion, and cost reduction initiatives from identification through implementation while working with cross functional resources to ensure results are achieved in a timely manner. | 03/10/2025 |
| 1555 | Baxter Marion, NC Associate II Quality Lab Chem FN Master’s Degree in Natural Sciences Exp: 0-3 years |
Conduct qualitative and quantitative chemical analysis on raw materials, solutions, and components following approved Standard Operating Procedures and test methods in an accurate and timely manner. Ability to work under minimum supervision while meeting deadlines. | 03/10/2025 |
| 1556 | Baxter Round Lake, IL Senior Electrical Engineer - R&D Masters in Electrical or Electronics or related Engineering Exp: 1+ year |
As the Sr. Electrical Engineer, you will develop creative solutions to challenging problems associated with the design of our new and existing infusion system product portfolio. You will possess strong technical capabilities, an excitement and energy for product development, and a passion for their work and the impact it has on saving and sustaining the lives of patients. | 03/10/2025 |
| 1557 | Baxter Marion, NC Quality Lab Associate I - Endotoxin Master’s Degree in biological sciences Exp: 0-3 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 03/10/2025 |
| 1558 | Baxter Marion, NC Quality Lab Associate II - Endotoxin Master’s Degree in biological sciences Exp: 0-3 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 03/10/2025 |
| 1559 | Baxter Hayward, CA Tech III, MNF Formulation Bachelor’s degree Exp: 6 months |
The Manufacturing Technician III is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Manufacturing Technician III is expected to fully participate in both departmental projects and any quality working teams which may be applicable. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. Manufacturing Technician III has sufficient technical and administrative competence to organize and lead production activities, including demonstrating leadership in state-of-the-art cGMP compliance, and environmental health and safety skills. | 03/10/2025 |
| 1560 | Baxter Marion, NC Engineer I, Project Engineering B.S.in Engineering Exp: 0-1 year |
We are looking for an individual to support a highly automated facility in North Cove, North Carolina. As a member of the Engineering department, the role will provide technical expertise to support plant manufacturing processes as well as other departments within the plant. In this role, you will focus on the implementation and adaptation of existing technologies of automation and associated processes in a manufacturing environment. The successful candidate must be a self-starter willing to assist the production and production service teams with hands-on troubleshooting. | 03/10/2025 |
| 1561 | Bausch + Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 03/10/2025 |
| 1562 | Beam Therapeutics Durham, NC Manufacturing Associate / Senior Manufacturing Associate BS, MS a plus, in Life Sciences or Engineering Exp: 0-10 years |
Beam Therapeutics is looking for highly energetic Manufacturing Associates to support GMP operations in 2025 at our site in Research Triangle Park, NC. Reporting to Sr Leadership in Manufacturing, the successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and routine GMP Operations. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment. | 03/10/2025 |
| 1563 | Beckman Coulter Diagnostics Chaska, MN Scientist I Production Operations Bachelor's Degree in a Science field (preferably in Chemistry, Biochemistry, Biology) Exp: 0-2 years |
The Scientist I Production Operations for Beckman Coulter Diagnostics is responsible for following established operation procedures, maintaining appropriate training records for your role, sustaining a smooth flow of material, and the execution of work orders to on-time completion. This position is part of the Upstream Value Stream located in Chaska, MN, and will be on-site. In Upstream Value Stream, our goal is on-time delivery of cell culture, purifications, and conjugations to support on-time delivery of immunoassays to patients. You will be a part of the Upstream Value Stream focusing on Conjugations. If you thrive in a fast-paced dynamic role and want to work to build a world-class manufacturing organization—read on. | 03/10/2025 |
| 1564 | BD San Diego, CA Biochemist II - Bead Manufacturing Master’s degree in science-related field Exp: 1-3 years |
The Biochemist II, Beads Manufacturing must have working knowledge of fluorescence microparticle manufacturing. This role will conduct data analysis to solve complex problems with various factors. The Biochemist II is responsible for improving process efficiencies and product quality. This position will also support and participate in continuous improvement projects as identified by the leadership team and assigned by the Senior Manager. | 03/10/2025 |
| 1565 | BD El Paso, TX Ld Tech. QA Bachelor’s degree Exp: 1+ years |
Lead Technician in Quality Assurance assures consistent quality of production by developing and enforcing good manufacturing practice (GMP) systems and support on validation activities. | 03/10/2025 |
| 1566 | Alcami Morrisville, NC Manufacturing Technician II (Sterile Injection) Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician II (Compound/Fill/Finish) is accountable for results in a fast-paced environment and assists with the manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. The Manufacturing Tech II is a key role responsible for executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology. This position entails a high level of technical expertise in aseptic processes requiring single-use components, ability to troubleshoot, and responsibility for maintaining quality and compliance with Good Manufacturing Practices (GMP). The Manufacturing Tech. II performs the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Tech. II employs acceptable techniques while working in manufacturing environments, including PPE gowning. The candidate must have the ability to learn specific department procedures, have a general understanding of Good Documentation Practices (GDP) and GMP, and follow directions from leadership/peers to ensure manufacturing goals are met. | 03/05/2025 |
| 1567 | Alcon Forth Worth, TX Senior Scientist - Ocular Health (Formulation Development) Master's Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon and we are looking for a Senior Scientist - Ocular Health (Formulation Development) in Fort Worth, TX. The Senior Scientist will lead and contribute to the research and development of new formulations and biomaterials, focusing on novel ophthalmic materials development. This role supports the advancement of extraocular and intraocular materials. The Senior Scientist will play a key role in developing innovative solutions for topical ophthalmic products such as artificial tear and contact lens care solution. This position involves formulating and optimizing products with an emphasis on surface interaction, material-cellular interaction, structure-property relationship. The ideal candidate will have substantial experience in formulation development. | 03/05/2025 |
| 1568 | Alcon Johns Creek, GA Opto-Mechanical Engineer Master’s degree Exp: 0+ years |
The Opto-Mechanical Engineer designs, models, analyzes, and tests optical, electro-optical, and opto-mechanical systems and components, including sensors, lasers, fiber-optics, and telecommunications products. Conducts research and development into phases of physical optics and geometric optics, lasers, laser characteristics, laser maintenance, and broadband optical sources. Applies research of complex optical systems to achieve desired optical outcomes. Develops component specifications, tolerances, simulations and tests procedures for electro-optical systems and components. Uses design-to-cost models, six sigma methodology, and other methods to assure and verify optical design requirements are met. | 03/05/2025 |
| 1569 | Alcon Houston, TX Controls System Engineer Master’s degree Exp: 0+ years |
As a Control Systems Engineer supporting our manufacturing site, you will be trusted with providing engineering skills and support to help develop software and hardware control solutions and for the design, programming, installation, modification, troubleshooting, and improvement of major systems at Houston, TX. | 03/05/2025 |
| 1570 | Alcon Johns Creek, GA Associate I, Quality Control Labs Bachelors’ Degree in Scientific Discipline Exp: 1-2 years |
Conduct Quality Control testing of materials and production samples as required to support contact lens production, performing assigned tasks according to approved SOP’s, methods, and procedures with adherence to cGMP, FDA, and Corporate Quality policies and regulations. Perform routine and non-routine incoming inspection procedures in generating information for the release of materials for production use, as well as to communicate the disposition of materials to internal and external customers (with minimal supervisory or designee direction). This position also assists in the solution of technical problems, with defined scope. | 03/05/2025 |
| 1571 | Alcon Johns Creek, GA Senior Mechanical Engineer Master’s degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As an Sr. Mechanical Engineer supporting the U.S. Development of Process and Piot Engineering Team in Duluth, GA, a typical day will include: Development, design, installation, commissioning, qualification and validation of new equipment, Communication and coordination with internal/external vendors during the implementation, commissioning, FAT and SAT, Provides expert level support and works with the various internal/external vendors/customers on key systems/deliverables, Collaborates and partners with associates from multiple disciplines, including Process Development, Research and Production, to ensure project success, Provides support, as needed, and generates required technical documentation including standard operating procedures (SOPs), training manuals and validation protocols in accordance with GMP guidelines, Identify, design and implement improvements to machines and processes related to support of contact lens development / manufacturing, Troubleshoot and correct issues related to complex production equipment used in the contact lens development / manufacturing process, Design and execute protocols for product development, and prepare documentation related to procedures, training, work instructions, validations, reports, etc., Support maintenance plans/spare part infrastructure to ensure that the required spare parts are available to reduce machine down times | 03/05/2025 |
| 1572 | Aldevron Fargo, ND Quality Control Analyst I, Environmental Monitorin Bachelor’s degree in microbiology or related scientific field Exp: 0-1 years |
This position is part of the Quality Control department located in Fargo, ND and will be an on-site position. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Quality Control Environmental Monitoring Team and report to the QC Environmental Monitoring Supervisor, and be responsible for sampling, detecting, quantifying, and identifying possible contaminants that may interfere with the quality of the product during the different stages of the manufacturing process. | 03/05/2025 |
| 1573 | Aldevron Fargo, ND Scientist I R&D MS degree in biology, molecular biology, biochemistry, chemistry, or related discipline Exp: 1+ years |
This position is part of the R&D department located in Fargo, ND and will be on-site. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Analytical Method Development unit and report to the Director, Analytical Development responsible for mRNA Analytics. | 03/05/2025 |
| 1574 | Alexion Durham, NC Sr. Associate Scientist I, Vector Production, Viral Vector Product Development Master’s degree in biology, or a relevant field Exp: 1-2 years |
This position will play a key role in Alexion’s Viral Vector Product Development, Vector Production team, interacting with internal teams within the Genomic Medicine and Product Development Clinical Supply groups. The senior associate scientist will be responsible for supporting both upstream and downstream AAV manufacturing. | 03/05/2025 |
| 1575 | AlivaMab Biologics San Diego, CA Research Associate I, Molecular Biology BS in Molecular Biology, Biomedical Engineering, or a related scientific field Exp: 0-3 years |
AlivaMab Biologics is seeking an outstanding individual to join our Antibody Engineering Team to support molecular cloning for the generation of expression constructs. As part of an interdisciplinary research team, the selected individual will be a key contributor to the progression of exciting antibody discovery and engineering efforts and contribute to technological development in the Molecular Biology group. This position will report to the Senior Scientist, Antibody Engineering, and work closely with scientists in the Protein Sciences and Antibody Discovery teams. | 03/05/2025 |
| 1576 | Alkermes Waltham, MA Healthcare Compliance Associate BS/BA Exp: 1-2 years |
The Healthcare Compliance Associate will report to the Director of Healthcare Compliance on the Compliance Monitoring and Auditing Plan. This position will require extensive domestic travel and will play an important role in fostering a culture of compliance. | 03/05/2025 |
| 1577 | Alkermes Wilmington, OH Manufacturing Process Technologist BS Degree in Engineering, Chemistry or Biology Exp: 1-2 years |
In the assigned manufacturing area, directly supports the Aristada Manufacturing Process. Actively supports ongoing manufacturing efforts in terms of quality and efficiency, provides an interface with Development and Engineering in technology transfer of new processes and process upgrades to existing technologies, and supports Corrective and Preventive Action programs. Conducts real-time monitoring/trending of manufacturing processes and finished product analytical data. | 03/05/2025 |
| 1578 | Alkermes Waltham, MA Sr. Research Associate II, Electrophysiology MS degree Exp: 1-5 years |
The Neurophysiology Group within the Research and Development organization is searching for an experienced electrophysiologist to support novel drug discovery research in CNS disorders. This position will be part of a larger multidisciplinary team challenged with interrogating the pharmacological properties and synaptic mechanism(s) of action of compounds in a variety of neuronal systems. Individuals with exceptional neurophysiology experience are encouraged to apply. The ideal candidate will have neuroscience research experience employing a variety of in vitro/in vivo electrophysiology techniques including traditional whole-cell patch-clamp, extracellular field potential recordings, and qEEG. Additional computational or programming experience is also required. Highest priority will be given to candidates with a strong desire to be in the laboratory designing and conducting experiments to support discovery projects. | 03/05/2025 |
| 1579 | ALSTEM Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 03/05/2025 |
| 1580 | Altasciences Columbia, MO Laboratory Supervisor Bachelor’s degree in a scientific discipline Exp: 0-3 years |
Responsible for managing Research Associates and assisting Scientists on studies/projects. Assists with training other laboratory staff in technical procedures. Assist with evaluating and optimizing the utilization of laboratory resources to attain operational goals, meet study deadlines, and deliver quality results. Works with Laboratory Sciences Senior Manager of Operations in formulating current and long-range plans, objectives and policies. | 03/05/2025 |
| 1581 | Altasciences Everett, WA Scientist, Ligand Binding Assays MS Exp: 1 year |
The Scientist, LBA provides technical and scientific expertise in ligand binding assays for method development, validation/qualification and execution of analytical projects in support of preclinical /clinical studies. The Scientist will ensure the overall integrity/quality of assigned studies. The Scientist can also be designated as the main contact for client interactions laboratory for their assigned projects. | 03/05/2025 |
| 1582 | Altasciences Columbia, MO Scientist Bachelor’s degree in Immunology/ Biology/ Chemistry or equivalent discipline Exp: 6 months |
Are you looking for your next profession in Preclinical studies? Start your career with Altasciences while working in our new state-of-the-art laboratory! Altasciences has just completed an 8,000-square-foot expansion of our laboratory in Columbia, MO and we are looking for exceptional analysts to join our growing team. You will assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. You will also support and perform data collection activities including ligand binding assays, and/or flow cytometry, and/or cell-based assays, and/or mass-spectrometry. We are hiring for all levels of Scientist, so apply today! | 03/05/2025 |
| 1583 | Altasciences Everett, WA Research Associate - Laboratory Sciences Bachelors degree Exp: 6 months |
Assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. Support and perform data collection activities including LC-MS/MS, qPCR, DNA isolation, ligand binding assays, and flow cytometry, as assigned. | 03/05/2025 |
| 1584 | Lighthouse Laboratory Services Greenville, NC LCMS Laboratory Technologist B.S. in chemistry, physics, toxicology, biochemistry, biological science, clinical laboratory science, or related field. Exp: 1 year |
This is an exciting opportunity for growth within the lab industry! Lighthouse Laboratory Services is seeking a highly motivated and experienced Full Time LCMS technologist to join our laboratory in Greenville, NC. The technologist will be responsible for the day-to-day operations of the toxicology laboratory, sample prep and processing, ensuring the delivery of high-quality testing services, and daily laboratory operations. | 03/05/2025 |
| 1585 | Lighthouse Laboratory Services Dickson, TN LCMS Laboratory Technologist B.S. in chemistry, physics, toxicology, biochemistry, biological science, clinical laboratory science, or related field. Exp: 1 year |
This is an exciting opportunity for growth within the lab industry! Lighthouse Laboratory Services is seeking a highly motivated and experienced Full Time LCMS technologist to join our laboratory in Dickson, TN. The technologist will be responsible for the day-to-day operations of the toxicology laboratory, sample prep and processing, ensuring the delivery of high-quality testing services, and daily laboratory operations. | 03/05/2025 |
| 1586 | AltPep Corporation Seattle, WA Senior Research Associate Master’s degree Exp: 1+ years |
We are seeking a meticulous and dynamic Senior Research Associate to join our translational chemistry team. As part of this role, you will be responsible for conducting and supporting laboratory research, ensuring the highest standards of quality and precision. Your contributions will be critical to the success of our research and development efforts, and you will have opportunities to work both independently and collaboratively within our innovative team. | 03/05/2025 |
| 1587 | Alvogen Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline Exp: 0-3 years |
Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. | 03/05/2025 |
| 1588 | Ambry Genetics Corporation Aliso Viejo, CA Automation Technologist II BS and/or MS degree in a life sciences field: Biology, Bioengineering, Molecular Biology or related field Exp: 1+ years |
The primary duties of this position are to assist other Automation Team members in assay automation development, as well as support the Clinical Laboratory by aiding in recovery and troubleshooting validated laboratory instruments. This position also plays a role in designing, optimizing, validating, maintaining, and troubleshooting automation tools for our clinical diagnostic assays. | 03/05/2025 |
| 1589 | Amneal Piscataway, NJ Scientist, Quality Control Master Degree (MBA) Chemistry or related science discipline Exp: 1+ years |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 03/05/2025 |
| 1590 | Amneal Branchburg Township, NJ Scientist, Quality Control Technical Services Master Degree (MBA) in Chemistry or related science discipline Exp: 1+ years |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 03/05/2025 |
| 1591 | AstraZeneca Waltham, MA Scientist, Oncology Bioscience MS in Biology, Oncology, Biochemistry, Pharmacology, Immunology or a related field Exp: 1+ year |
Would you like to apply your expertise to impact drug development in a company that follows the science and turns ideas into life-changing medicines? Then employment at AstraZeneca might be the right choice for you! We are seeking a highly motivated Scientist in Oncology Targeted Discovery with strong scientific and technical expertise in oncology research and a track record of scientific excellence to join our team in Waltham, MA USA. As a Scientist in our Oncology R&D department, you will be a key member of a team focused on supporting oncology projects through the drug discovery and development process. You will bring your theoretical and practical expertise in cancer biology to establish assay systems and deliver datasets that will have a direct impact on targeted therapeutics. | 03/05/2025 |
| 1592 | Andelyn Biosciences Columbus, OH GMP Scientist I BS Exp: 0+ years |
The GMP Operations Scientist I is responsible for supporting all aspects of Good Manufacturing Practices (GMP) production in the Clinical Manufacturing Facility (CMF). Working in collaboration with the manager of GMP operations and staff, the scientist, I will provide hands-on assistance for all day-to-day GMP production operations, including the execution of production processes, documentation, and facility and equipment maintenance. The Scientist I will support production efforts to deliver all products in a timely, compliant, and fiscally responsible fashion by following appropriate practices, production documentation, and Standard Operating Procedures (SOPs) for manufacturing biological products. | 03/05/2025 |
| 1593 | Andelyn Biosciences Dublin, OH Scientist II Masters Exp: No exp |
A Scientist II, in Process Devlopment, will support upstream and downstream process development activities including responsibilities in bioprocessing and analytics. Working in close collaboration with PD leadership and PD scientists, scientist II will support the execution and completion of projects involving platform development, optimization, in-process characterization, and tech transfer following appropriate regulatory practices, timelines, documentation, and standard operating procedures. Prior experience in the purification of biologics is preferred. He/She will keep abreast with state-of-the-art technologies and scientific advancements in the field and participate in discussions on scale-up of processes, process qualification, and strategies for process improvement. | 03/05/2025 |
| 1594 | Andelyn Biosciences Dublin, OH Scientist I BS Exp: No exp |
The Scientist I position will support upstream and downstream process development and responsibilities in bioprocessing and analytics. The Scientist I will provide hands-on assistance for day-to-day process development production operations, including execution and development of production and purification processes, development of in-process assays for physical and functional characterization of the product, documentation, and participate in scientific discussions. | 03/05/2025 |
| 1595 | Ani Pharmaceuticals Baudette, MN Quality Control Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: 1-3 years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 03/05/2025 |
| 1596 | Ani Pharmaceuticals Baudette, MN QA Specialist I Bachelors degree is required. Chemistry, medical technology, microbiology Exp: 1-2 years |
This position is responsible for providing support to the Manufacturing and Packaging Operations to ensure relevant procedures are followed and meet GMP requirements. This includes, but is not limited to the following: Perform packaging line inspections/audits and provide assurance that packaging operations are compliant with applicable SOPs and cGMPs. Perform finished product attribute sample inspection and evaluation of finished products physical characteristics prior to packaging. Perform annual retain sample inspections and control finished product and raw material retain samples stored in the reserve sample room. Monitor GMP areas for compliance with general GMP requirements such as proper gowning and cleanliness, per CFR21 Subpart A General Provisions to assure they reflect current practices and meet industry standards and cGMP requirements. Perform other duties as assigned or requested. | 03/05/2025 |
| 1597 | Anika Bedford, MA QC Microbiologist I, Environmental Monitoring Bachelors Degree Exp: 1-2 years |
The QC Microbiologist I, Environmental Monitoring will learn, understand, and perform routine entry level sampling of cleanrooms and utilities according to written procedures under cGMP conditions; as well as tasks involved with clerical and logistical laboratory tasks. | 03/05/2025 |
| 1598 | Aquestive Warren, NJ Formulation Scientist MS in science Exp: 0-5 years |
A member of the R&D team responsible for the design and development of drug products for the targeted delivery of active pharmaceutical ingredients, including orally dissolving thin films for transmucosal delivery or lotions, ointments, and creams for topical delivery. | 03/05/2025 |
| 1599 | Ardena Somerset, NJ QC/EM Sampling Technician Bachelor’s Degree Exp: 1+ years |
This position is responsible for the timely sampling of incoming materials, supporting sample coordination activities and environmental monitoring of the facility and utilities at Ardena Somerset. | 03/05/2025 |
| 1600 | Ardena Somerset, NJ Senior Associate Microbiologist BS in Microbiology or related science. Exp: 1-3 years |
The Microbiology Department is responsible for performing microbial testing of raw materials and finished products (for clinical, commercial, and customer products) according to current compendia methodology. The Microbiology Department is also responsible for Environmental Monitoring of the facility and utilities at Catalent Somerset. The Senior Associate Microbiologist reports to the Microbiology Manager/Principal Microbiologist/Senior Microbiologist. This position contributes significantly to the successful timely testing and releasing of Raw Materials, in-process samples, and Finished Products of GMP and/or Commercial pharmaceutical Manufacturing. The primary responsibilities of this position will be performing microbial activities in support of the manufacturing of pharmaceutical products under the supervision of other microbiologists. These activities include raw material testing, in process testing, finished product testing, environmental sampling and testing, and water sampling and testing. | 03/05/2025 |
| 1601 | ARL Bio Pharma Oklahoma City, OK Chemist I - Analytical Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 03/05/2025 |
| 1602 | ARL Bio Pharma Oklahoma City, OK Chemist I - Chemistry Bachelor’s degree in chemistry or related science Exp: 0-2 years |
This position assists in maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position provides a backup for the daily calibration and/or verification of the balances and pH meter when the Lab Technician is unavailable. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform tests commensurate with skill level with some supervision. | 03/05/2025 |
| 1603 | ARL Bio Pharma Oklahoma City, OK Microbiologist I Bachelor’s degree in Microbiology or related science Exp: 0-2 years |
Under the supervision of the laboratory supervisor the Microbiologist I provides a high level of quality pharmaceutical microbiology testing as well as effective customer service to ARL Bio Pharma clients. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. | 03/05/2025 |
| 1604 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field Exp: 1-2 years |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 03/05/2025 |
| 1605 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist I, Discovery Chemistry Operations B.S. Chemistry or Biochemistry degree Exp: 0-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Scientist to join the Discovery Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, conjugation, purification, and characterization. They will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 03/05/2025 |
| 1606 | AbbVie Irvine, CA In Vitro Associate Scientist II MS Exp: No exp |
The In Vitro Associate Scientist II, as part of Local Delivery Translational Sciences (LDTS) at the Irvine, California site at AbbVie is responsible for developing and applying novel physiologically relevant in vitro models to characterize drug, biologic, formulation and sustained delivery formulation (e.g. sustained release implants) performance, erosion, and safety/tolerability. The In Vitro Associate Scientist II serves as a subject matter expert collaborating with colleagues in Clinical Pharmacokinetics, Pre-Clinical Safety, and other research functions to design in vitro experiments and develop novel in vitro models to address needs of AbbVie projects, specifically for botulinum toxin, eye care and aesthetics therapeutic areas. As a member of a small team, this individual will independently develop and perform in vitro and related bioanalysis studies, document experiments, prepare formal reports, and present findings to key stakeholders, This individual should be a self-starter who is eager to learn and thrives in a collaborative, fast-paced environment, with a desire to make an impact by interacting closely with scientists from other disciplines and functional areas. | 02/24/2025 |
| 1607 | AbbVie Irvine, CA Associate Scientist II - In Vivo Pharmacology Master’s Degree Exp: No exp |
The Neurotoxin Research Group at AbbVie is seeking a highly motivated and innovative candidate for the role of Associate Scientist II, In vivo pharmacology. The successful candidate for this position will contribute to projects aimed at the pharmacological characterization of protein-based therapeutics. Under supervision by senior personnel, he/she will be required to work on a variety of in vivo animal pharmacology models to help characterize and evaluate biological compounds. This individual will need to organize, analyze, interpret, and present results to senior personnel or in team meetings. A good understanding of animal models, neurology, and pharmacology is required. Experience in handling and injecting rodents by different routes is required. Working knowledge of neuroscience and in vivo motor pharmacology is an advantage. The successful candidate will be collaborating extensively with other Research Associates and Scientists, while taking personal responsibility for the success of assigned tasks and projects. | 02/24/2025 |
| 1608 | AbbVie Worcester, MA Associate Scientist II/ Scientist I, Gastro Pharmacology Master’s Degree Exp: No exp |
We are looking for a highly motivated scientist to join our Gastroenterology Disease Area Team in Discovery Research Immunology located in Worcester, MA. The ideal candidate should be independently driven, highly collaborative, and results oriented. They will support in vitro and in vivo research efforts for our existing early-stage through late-stage discovery portfolio programs. Responsibilities include conducting, analyzing, and reporting on in vitro and in vivo assays to explore key biological questions related to IBD diseases, such as ulcerative colitis and Crohn’s disease. The candidate should be proficient in basic laboratory techniques such as pipetting, cell culture, flow cytometry, qPCR, and ELISA. The ideal candidate should also have hands-on experience with in vivo PK/PD rodent studies as well as substantial experience culturing and designing functional assays with primary human cells (e.g. proliferation, differentiation, co-culture). | 02/24/2025 |
| 1609 | Abeona Therapeutics Cleveland, OH Analyst Quality Control Micro Analytical BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 1-3 years |
The Quality Control Analyst I performs routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Performs in-process and release testing for drug substance and drug product. Interacts with employees internal and external to Quality Control. | 02/24/2025 |
| 1610 | Abeona Therapeutics Cleveland, OH Associate, Manufacturing - Operations MS in scientific discipline Exp: 1-2 years |
Abeona is looking for a Manufacturing Operations Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector and autologous gene-corrected cell therapies. Responsibilities will include executing protocols and manufacturing clinical and commercial material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. | 02/24/2025 |
| 1611 | Abeona Therapeutics Cleveland, OH Document Control/Archivist Specialist I, Quality Assurance Bachelor’s degree in related field Exp: 1-3 years |
The Specialist I, Quality Assurance performs routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position is responsible for document review which includes, but is not limited to: editing, formatting, and proofreading prior to SME approval in the Quality Management System. This position is also responsible for document archival and retention post product disposition. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above and will support all document review and retention/archiving for the site. | 02/24/2025 |
| 1612 | Abeona Therapeutics Cleveland, OH Quality Control Analyst I (QC Analytical) BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 1-3 years |
The Quality Control Analyst I performs routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Testing includes qPCR, immunostaining, protein characterization and product specific analytical test methods. Interacts with employees internal and external to Quality Control. | 02/24/2025 |
| 1613 | Abeona Therapeutics Cleveland, OH Specialist I, Quality Assurance Bachelor’s degree in related field Exp: 1 year |
The Specialist I, Quality Assurance performs routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the maintenance of the quality systems in support of a cGMP Operations, corrective and preventative actions, quality events management (e.g., nonconformances, deviations, etc.), training, document management and ensuring procedural and regulatory compliance throughout the manufacturing process. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above. | 02/24/2025 |
| 1614 | Adare Pharma Solutions Vandalia, OH Analytical Scientist I or II Master’s Degree in Chemistry or related discipline Exp: 0-1 years |
The Analytical Scientist I or II will support the development and validation of analytical methods for raw materials, work-in-process, and finished products to provide testing support for the formulation development and clinical supplies release process. The Scientist II will also be expected to provide some training, coaching, and mentoring for more junior scientists. | 02/24/2025 |
| 1615 | Adesis New Castle, DE Research Chemist Bachelor of Science Exp: 1-2 years |
Responsible for assisting chemists in performing various purifications of target compounds using various methods, including, but not limited to preparative high performance liquid chromatography (prep HPLC), normal phase and reverse phase chromatography, and recrystallization. | 02/24/2025 |
| 1616 | ADMA Biologics Boca Raton, FL Laboratory Technician - Automation Bachelor’s degree in related science discipline Exp: 0-2 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We have an exciting opportunity available for a Laboratory Technician - Automation in Boca Raton, FL! The Laboratory Technician - Automation performs automated laboratory testing to support hyperimmune products for ADMA Biologics. This position is responsible for the receipt, testing and on-time delivery of donor testing and maintaining a cGMP compliant laboratory. Maintaining communication with group leader or department manager to support cross-function relationships with plasma centers and ADMA plasma operations. | 02/24/2025 |
| 1617 | ADMA Biologics Boca Raton, FL Scientist II Process Development Master’s degree in biochemistry, chemical engineering, biophysics, biology, or a related field. Exp: 0-5 years |
We are excited to offer a new opportunity for a Scientist II, Process Development based in Boca Raton, FL! In this role, the Scientist II, Process Development will contribute to the advancement of protein purification processes, playing a key part in our development efforts. | 02/24/2025 |
| 1618 | Admera Health South Plainfield, NJ Associate Scientist I/II (Lab) Bachelor’s degree or MS in Biological Sciences Exp: 1-3 years |
Preparing solutions and reagents for performing assays on the bench. Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq. Whole Genome Sequencing. Whole Exome Sequencing. Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. Strict recordkeeping of all laboratory procedures. Continue acquiring next generation sequencing knowledge to support molecular biology techniques. Collaborate within the group and cross departmental to achieve goals. | 02/24/2025 |
| 1619 | ABS Livermore, CA Operations Engineer B.Eng in Mechanical Engineering, Industrial Engineering, Manufacturing, or related discipline. Exp: 1-3 years |
Reporting to the Director, Engineering & Operations, the Operations Engineer will have responsibility for key aspects of ABS’ product manufacturing and operational processes. Assuming the dual roles of that of a Manufacturing Engineer and Facilities Engineer, the Operations Engineer will work on simple-to complex, high visibility/value projects with a focus on supporting production. The Operations Engineer will also support the Facilities function in a multitude of ways – compliance, procedure development, equipment maintenance, organization and much more. | 02/24/2025 |
| 1620 | Advanced Instruments Norwood, MA Mechanical Engineer I Bachelor’s degree in mechanical engineering. Exp: 1-3 years |
As a Mechanical Engineer I you will work on new product development and/or sustaining engineering tasks, prepare electro-mechanical designs, drawings, specifications for new and sustaining product lines, and provide technical guidance and expertise to projects within the R&D department as well as Manufacturing Engineers and production personnel. The Mechanical Engineer I will report to the Mechanical Engineering Manager as an individual contributor and must be capable of working with senior level engineers. You will complete detailed specifications, designs, calculations, analyses and simulations for major hardware components of a project. In this role, you will be capable of working on assembly of models and prototypes in engineering lab environment and set up and conduct non-standard or product-specific evaluation tests of prototypes. You will record observations and data, analyzes and interprets results and prepares summary reports. | 02/24/2025 |
| 1621 | New Age Industries Southampton, PA Project Engineer B.S. in Engineering (Mechanical, Chemical, Materials Science, Biomedical preferred). Exp: 0-3 years |
The Project Engineer utilizes his or her technical, project management, and problem-solving skills to organize group efforts and execute tasks towards company goals in areas such as new product development, supply chain/change management, manufacturing, and continuous improvement efforts. The Project Engineer must use software tools to create and maintain measurable progress metrics that can be communicated regularly to stakeholders. | 02/24/2025 |
| 1622 | B. Braun Medical Inc. Daytona Beach, FL QC Lab Tech II-Microbiology Bachelor's degree Exp: 1-2 years |
Performs a variety of quality control tests on products at various stages of the production process to ensure compliance with quality and reliability standards. Records statistical data. Analyzes data and writes summaries to validate or show deviations from existing standards. Recommends modifications to existing or suggests new, standards, methods and procedures. | 02/24/2025 |
| 1623 | B. Braun Medical Inc. Irvine, CA QC Chemistry Associate II Bachelor's degree in a Science related field Exp: 1-2 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 02/24/2025 |
| 1624 | Affinia Therapeutics Waltham, MA Research Associate, Preclinical Analytics Master's Degree Exp: 1-4 years |
Affinia Therapeutics is seeking an experienced Research Associate (job level will commensurate with experience) to join our Preclinical Analytics laboratory team. You will be part of a group dedicated to the advancing of gene therapies based on vectors derived from our unique AAV platform. You will actively contribute to the development and execution of analytical assays supporting studies conducted by the translational science team at Affinia. You will work to establish methods and analyze samples to meet timelines for our internal development programs. You will contribute to the evaluation of new analytical technologies, the development of more efficient laboratory workflows as well as maintaining a culture of quality and excellence. | 02/24/2025 |
| 1625 | AGC Biologics Bothell, WA Quality Control Associate I, Sample Management BS/BA degree Exp: 0-2 years |
Performs basic QC analysis and documents activities according to SOPs following good manufacturing processes (GMP) and demonstrates ability to learn QC methods, procedures and systems. | 02/24/2025 |
| 1626 | AGC Biologics Boulder, CO MSAT Engineer I/II BS in Chemical engineering / Biochemical engineering / Biology or other science related discipline Exp: 1 year |
We have an opportunity for an MSAT Engineer I/II to join the Manufacturing Science and Technology (MSAT) team at AGC Biologics in Boulder, CO. This position requires technical problem-solving and inter-departmental collaboration. Responsibilities will be varied, requiring time management skills and ability to deliver against fluid timelines. This role is responsible for 24/7 production support when manufacturing operations are in progress including direct Person in Plant and customer support. Other responsibilities include technology transfer support, new proposal support, quality systems support and data collection, trending, and analysis support. | 02/24/2025 |
| 1627 | AGC Biologics Boulder, CO Quality Control Associate I, Sample Management BA in Biology, Microbiology, or other scientific discipline. Exp: 0-2 years |
The Quality Control Associate I - Microbiology will focus on performing microbial and environmental monitoring assays, facility qualification, and testing of purified water and cleaning samples. This position may also review data, execute validation studies, and support commissioning of laboratory instruments. The ideal candidate will be highly motivated, organized, and have the ability to work independently. Experience in a GMP Microbiology laboratory is preferred. | 02/24/2025 |
| 1628 | AGC Biologics Bothell, WA Manufacturing Support Technician I BS/BA degree Exp: No exp |
As the Night Shift GMP Cleaning and Sanitization Technician, you will be responsible for maintaining the cleanliness and compliance of GMP regulated areas and ensuring facilities are properly restocked. You will also be expected to follow and document all sanitization processes in line with our SOPs and regulatory requirements. | 02/24/2025 |
| 1629 | AGC Biologics Bothell, WA Upstream Manufacturing Associate I/II BS/BA degree Exp: 0-2 years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor, and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. | 02/24/2025 |
| 1630 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I/II BS/BA degree Exp: 0-2 years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor, and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. | 02/24/2025 |
| 1631 | Agilent Boulder, CO Manufacturing Associate - Representative Bachelor’s or Master’s Degree Exp: 1+ years |
As a Manufacturing Associate, you will check and schedule resources to ensure timely delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. You will have an opportunity to become skilled in the use of a wide range of lab instruments, including but not limited to spectrophotometers, conductivity meters and auto-pipettors, all of which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are essential. Additionally, you will work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. You will also exercise judgment within generally defined practices and policies in selecting methods and techniques for acquiring solutions. | 02/24/2025 |
| 1632 | Agilent Carpinteria, CA Research Associate, Entry Bachelor’s Degree or Higher, or equivalent in a scientific discipline. Exp: No exp |
We are looking for a talented and dedicated Research Associate to join the CDx Group in our R&D Department. You will provide technical support to develop accurate, robust and precise assays. Your challenge will be to create value for Agilent through innovative ideas that either create new businesses or enhance existing ones. | 02/24/2025 |
| 1633 | Agilent Newport, DE Production Chemist – Particle Engineering Bachelors or Masters Degree in Chemistry, Material Science or equivalent Exp: 1+ years |
Agilent Technologies is seeking a Production Chemist for its manufacturing facility in Newport, Delaware. The Newport site is part of Agilent’s growing Consumables and Supplies Division (CSD), with a focus on liquid chromatography products. Agilent’s product quality and technological innovation lead the market. As a leader, we are entering new phases of product transformation with increased emphasis on new product and process innovation, process standardization and production efficiency. | 02/24/2025 |
| 1634 | Agilent Cedar Creek, TX Manufacturing Scientist - Genomic Reagents Testing Bachelor's degree or equivalent experience in Biological Science or a related field with chemistry, molecular biology, or biochemistry expertise. Exp: 1 year |
Join our innovative team at Agilent Technologies as a Manufacturing Scientist specializing in genomic reagents. You'll contribute to ground breaking products that advance Next Generation Sequencing (NGS), Microarray testing, and PCR-based technologies. If you're passionate about driving scientific advancements and thrive in a dynamic, collaborative environment, this role offers an exciting opportunity to grow and make a tangible impact. | 02/24/2025 |
| 1635 | Agilent Frederick, CO Manufacturing Associate Bachelor’s or Master’s Degree Exp: 1+ years |
As a Manufacturing Associate (Representative), you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. You will have an opportunity to become skilled in the use of a wide range of lab instruments, including but not limited to spectrophotometers, conductivity meters and auto-pipettors, all of which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are critical. Additionally, you will work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. You will also exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. | 02/24/2025 |
| 1636 | Agilent Cedar Creek, TX Manufacturing Scientist - NGS Probe BS/BA in Biological Science or related field with experience in chemistry, molecular biology, and/or biochemistry. Exp: 1+ years |
Join our Next Generation Sequencing (NGS) Probe manufacturing team as a Manufacturing Scientist at Agilent Technologies. At Agilent Technologies, we are dedicated to advancing scientific discoveries that improve the quality of life. Our Manufacturing group is a collaborative and diverse team made up of members who learn quickly on the job and anticipate/resolve potential manufacturing issues while maintaining the highest level of quality. This is essential in delivering innovative, high-quality products to our customers worldwide. | 02/24/2025 |
| 1637 | Agilent Boulder, CO Manufacturing Chemist Bachelor's degree in chemistry, biology, engineering or related life science field Exp: 1+ years |
The Manufacturing Chemist position performs a wide variety of technical duties to support small scale manufacturing operations. | 02/24/2025 |
| 1638 | Ajinomoto Bio-Pharma San Diego, CA Drug Product Manufacturing Associate I Bachelors in a science or engineering discipline Exp: 0-2 years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 02/24/2025 |
| 1639 | Ajinomoto Bio-Pharma San Diego, CA QA Associate I Bachelor’s degree in a Life Sciences discipline Exp: 0-2 years |
We are currently seeking QA Associate I who is responsible for performing a wide variety of routine and semi-routine activities pertaining to assuring compliance with Quality Assurance (QA) requirements and applicable regulatory requirements. The Associate I promotes a cGMP environment and collaborates with internal team members to ensure adherence to specifications, processes, and procedures. The Associate I performs documentation review and ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. Understanding and execution of basic cGMP and GDP principles is required. | 02/24/2025 |
| 1640 | Akoya Biosciences Marlborough, MA Research Associate II, Histology BS Degrees in Life Sciences preferred Exp: 1-2 years |
Akoya is seeking a Research Associate II (RA-II) to work within our Akoya Advanced Biopharma Solutions (ABS) CLIA laboratory located in Marlborough, MA. This position is a full-time onsite role. The candidate will have worked in a clinical or preclinical pathology laboratory with experience in high-throughput histology with focus on immunohistochemistry. The candidate will work with lab personnel on histology processes such as grossing, processing, embedding, and microtomy. Knowledge of antibody validation methods, immunofluorescence (IF) and quantitative pathology approaches are a plus but not required. The successful candidate must have significant experience in microtomy, preferably with rotary microtomes. They should also be familiar with LIMS systems and have experience working in a regulated laboratory setting such as CAP/CLIA and GCLP. | 02/24/2025 |
| 1641 | Akron Biotech Sarasota, FL Associate, Manufacturing - Operations BA/BS in Biology, Chemistry, Bioengineering or a related field Exp: 1-2 years |
Akron Biotech is continuing to transform and further its rapidly growing capabilities and is now seeking highly motivated professionals to join our expanding team. This is an exciting opportunity to play a critical role within our organization that is driving advanced therapy development and commercialization with high quality industrial scale solutions. We manufacture and distribute components and raw materials for cell therapy discovery, development, and commercialization to meet industry needs worldwide. We offer an array of highly competitive benefits and perks to our valued associates. | 02/24/2025 |
| 1642 | Akston Biosciences Beverly, MA Research Associate I/II Bachelor’s degree in Engineering, Biology, Molecular Biology, Pharmaceutical Sciences or related field Exp: 0-3 years |
Akston is looking for a highly motivated and energetic Research Associate I/II to join our dynamic and diverse R&D team. In this role, you'll play a key part in supporting our efforts to develop innovative biologic therapies. The ideal candidate will collaborate closely with cross-functional teams, translating strategic goals into actionable plans. Experience with biological entities (e.g., fusion proteins and monoclonal antibodies) is essential. A background in analytical chemistry, biochemistry, biotechnology, chemical biology, chemical engineering, molecular biology or related fields is highly desirable. | 02/24/2025 |
| 1643 | Alcami Morrisville, NC Environmental Monitoring Technician I - 2nd Shift BS Exp: 0+ years |
The Environmental Monitoring Technician I is accountable for driving results in fast-paced environment by performing monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The Environmental Monitoring Technician must be detail-oriented and possess organizational skills with a large quantity of data. | 02/24/2025 |
| 1644 | Alcami Morrisville, NC Environmental Monitoring Technician I - 1st Shift BS Exp: 0+ years |
The Environmental Monitoring Technician I is accountable for driving results in fast-paced environment by performing monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The Environmental Monitoring Technician must be detail-oriented and possess organizational skills with a large quantity of data. | 02/24/2025 |
| 1645 | Alcami Morrisville, NC Scientist II - Compendial Testing, Raw Material Master’s degree Exp: 0+ years |
The Scientist II / III is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Scientist II / III may also be required to work on method development/method validation projects. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). | 02/24/2025 |
| 1646 | TScan Therapeutics Waltham, MA Clinical Trial Associate BS in scientific or healthcare discipline Exp: 1-3 years |
TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a Clinical Trial Associate to join our Clinical Operations team to support the execution of our Phase 1 basket study in solids. The ideal candidate should have experience in supporting the execution of oncology clinical studies as well as a working knowledge of ICH GCP regulations. The candidate should a enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 02/17/2025 |
| 1647 | Ultima Genomics Fremont, CA Product Engineer I BS or MS in Computer Science, Engineering, Biomedical, Electrical, Mechanical, Systems Engineering disciplines or core scientific degree Exp: 1 year |
Our Product Engineer plays a strategically important role in ensuring the company’s business success. The primary responsibilities include, but are not limited to, supporting Field Service Engineers (FSEs) and Field Application Scientists (FASs) groups with technical support, authoring and reviewing Best Known Practices (BKPs) for field deployment, and coordinating the rollout and implementation of Engineering Change Orders (ECOs) in the field. In this Product Engineer (PE) position, you will train FSE’s on best practices and be the point of contact for field escalations. PEs are system experts and sometimes work side by side with R&D to gain a deep understanding of the system. PEs will help define problem statements, develop mitigations, and are a key contributor to Corrective Action Preventative Action (CAPA) plans. | 02/17/2025 |
| 1648 | United Therapeutics Research Triangle Park, NC Bioprocess Technician - Tissue Engineering Development Bachelor’s Degree in life science, engineering, or biomedical science Exp: 1+ years |
If you're passionate about advancing research for the treatment of pulmonary hypertension and other lung diseases, this role is for you! As part of our innovative research team, you’ll play a pivotal role in developing regenerative medicine products by operating lung recellularization systems and supporting tissue engineering processes. You’ll assist in preparing human and non-human tissues, performing assays, maintaining bioreactors, and analyzing data—contributing directly to the development of groundbreaking treatments. If you thrive in a collaborative, hands-on lab environment and are eager to apply your technical skills to real-world medical solutions, this position offers a unique opportunity to make a meaningful impact. | 02/17/2025 |
| 1649 | United Therapeutics Research Triangle Park, NC Assembly Technician I Bachelor’s Degree Exp: 1+ years |
As a key member of our R&D team, you will contribute to the preparation and assembly of medical and laboratory device components, playing a crucial role in the advancement of our projects. You’ll work hands-on in the lab to assemble tubing sets, prepare cell culture media, ensure sterilization, and maintain an organized and safe environment, all while following detailed instructions to support the development of next-generation medical devices and technologies. | 02/17/2025 |
| 1650 | Unither Rochester, NY Validation Technician BS Exp: 0 years |
Assists validation efforts in many ways including the following: executes/supports equipment, cleaning, and process qualifications, takes and delivers samples, collects and compiles data for validation reports, assists in maintaining of the Validation Document Library, maintains test equipment and documentation system. | 02/17/2025 |
| 1651 | Vala Sciences San Diego, CA Research Associate (RA)/Senior Research Associate (SRA) – iPSC Manufacturing B.S. or M.S. in Cell/Molecular Biology, Biochemistry, Neuroscience, or related field Exp: 1-2 years |
We’re seeking an RA or SRA to join our dynamic induced pluripotent stem cell (iPSC) research and manufacturing program. The successful candidate will manage iPSC lines and their differentiation to different cell types, like cardiomyocytes, microglia, neurons, and astrocytes. These differentiated iPSC lines will be used for internal R&D projects, commercial research contracts, and manufacture for sale. You will evaluate and validate differentiated cell lines with biomarker detection methods like ICC or flow cytometry, and investigate and characterize cellular function using Vala’s live-cell fluorescent imaging technology. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 02/17/2025 |
| 1652 | Vantage MedTech Lenexa, KS NPI Engineer BS or MS degree in Engineering, preferably Mechanical or Manufacturing Engineering. Exp: 1-3 years |
The NPI (New Product Introduction) Engineer will be responsible for ensuring that our innovative designs are transitioned into effective and sustainable production. Our life saving products are manufactured in Kansas City and require predictable delivery of high quality, cost-effective production over 5+ year product lifetimes. You will collaborate with Vantage MedTech’s Engineering and Manufacturing teams to provide input on the device design’s manufacturability, and plan and execute the transfer of these new products to our manufacturing facility. You will be responsible for ensuring that robust manufacturing processes are created, updated and in compliance with company standards, ISO, and GMP as required. In addition, you will help drive improvement projects that impact quality and productivity. | 02/17/2025 |
| 1653 | Vaxcyte San Carlos, CA Associate Scientist I, Formulation Development BS in Pharmaceutical Sciences, Organic/ Biochemistry, Chemical / Biochemical Engineering, Biology, Chemistry or a related discipline Exp: 0-2 years |
Vaxcyte is looking for an energetic and talented individual to play a key supporting role in the Formulation Development function. Vaxcyte is focused on the development of protein conjugate vaccines. They would support manufacture of drug products to support analytical and process development groups within the Drug Product Team. In addition, they would also support scientists in the execution of large and complex experimentation as well as routine studies and testing. | 02/17/2025 |
| 1654 | Vedanta Biosciences Cambridge, MA Contract - Research Associate, Analytical Development BS in a life science Exp: 1+ years |
Vedanta is seeking a research associate to join the Analytical Development Group, supporting the molecular biology team within Analytical Development. We are looking for an individual who is curious, intrinsically motivated, excited to collaborate, and an excellent communicator. | 02/17/2025 |
| 1655 | Veloxity Labs Peoria, IL Associate Scientist II Bachelor’s degree in science (chemistry/biochemistry preferred) Exp: 1-2 years |
As an Associate Scientist II, you will be using state-of-the art technologies to perform bioanalytical testing for emerging pharmaceutical and biopharma companies. At Veloxity, we hire driven and motivated individuals and provide training and career advancement opportunities within our organization. | 02/17/2025 |
| 1656 | Veracyte Austin, TX Specimen Processor Bachelor’s degree Exp: 0-2 years |
The Specimen Processor in this CLIA Laboratory is a critical member of the laboratory team, responsible for receiving, accessioning, and documenting specimens with precision. This role requires accurate data entry, proactive identification, and resolution of sample integrity issues. Flexibility in scheduling, including holidays and variable shifts, is essential to meet operational demands. | 02/17/2025 |
| 1657 | Vericel Cambridge, MA Associate I, Cell Therapy Manufacturing Bachelor’s degree (Life Sciences or related field) Exp: 0-2 years |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. | 02/17/2025 |
| 1658 | Vericel Cambridge, MA Quality Control Analyst, II Master’s Degree Exp: 0+ years |
Responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs for product release and validation. | 02/17/2025 |
| 1659 | Vericel Cambridge, MA Engineer, I Bachelor's degree in Chemical or Mechanical Engineering or a related engineering field. Exp: 0-2 years |
The Engineering department is primarily responsible for the detailed design, startup, troubleshooting, commissioning, optimization and lifecycle support of manufacturing equipment, facilities, and utility systems. | 02/17/2025 |
| 1660 | Versatope Therapeutics Lowell, MA Process Development Scientist Masters degree in biotechnology Exp: 0-5 years |
At Versatope Therapeutics you will work alongside other bright, motivated scientists in developing groundbreaking vaccines and therapeutics. We hire amazing people who are intensely curious and continually questioning. | 02/17/2025 |
| 1661 | Vigil Neuroscience Watertown, MA Scientist, Discovery Biology (Contract) M.S. Exp: 1+ years |
Vigil is looking for a skilled and motivated Scientist to join our team. The successful candidate will be responsible for execution of assays for novel therapeutics targeting neuroinflammation and neurodegeneration, with a primary focus on microglia. The ideal candidate is highly organized, independent, and collaborative. | 02/17/2025 |
| 1662 | Vivex Miami, FL Staff Quality Assurance Engineer Bachelor’s degree in engineering or a related technical discipline (e.g. Biology, Chemistry, etc.) Exp: 1 year |
The Quality Assurance Engineer develops, applies, revises, and maintains quality metrics to support areas of operations at Vivex Biologics, Inc. The role assists in the planning, development, implementation, communication, and maintenance of Vivex’s quality management systems, polices, documentation, data, and customer requirements. The Quality Assurance Engineer is expected to work with all departments to ensure compliance, that the final products are safe, reliable, and effective, and the successful and timely completion of projects. The Quality Assurance Engineer is mainly responsible for the maintenance of CAPA system items. They play a key role in preventing issues or fixing them if they arise by defining, monitoring, and approving the processes needed to achieve production standards. | 02/17/2025 |
| 1663 | Vivex Miami, FL Operations Processing Technician I Bachelor’s Degree in science or related Exp: 0-1 years |
The Operations Processing Technician I support the processing and documentation requirements of tissue during the cleaning, cutting, shaping, inspecting, and packaging operations for transplantation purposes. The Operations Processing Technician I is also responsible for ensuring that all equipment and supplies used for processing are maintained and ready for use, and that all Processing Room maintenance is completed daily while complying with Quality Assurance requirements as mandated by federal, state, and trade regulations. | 02/17/2025 |
| 1664 | Vivex Miami, FL IC/QC & Distribution Coordinator I Bachelors Exp: 0-1 years |
The IC/QC & Distribution Coordinator I - Weekend Shift is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Ensure that Inventory Control Operations are in Compliance with the State and Federal Regulations and AATB Standards. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Resourceful in completing deadlines and can multitask effectively. | 02/17/2025 |
| 1665 | West Williamsport, PA Tooling Engineer Bachelor’s Degree in a technical discipline to include: mechanical engineering, manufacturing engineering, industrial, or plastics. Exp: 1-3 years |
The Tooling Engineers objective is to support the facility, commercial team, and mold tooling vendors on new mold development projects and legacy mold improvement projects. In parallel, the position also provides innovative solutions and services to the tooling group and other departments within the company, where possible, to assist with meeting company goals and objectives. In this role, you will be part of a team that relies on effective teamwork and global collaboration in a fast pace and dynamic environment. This role may be responsible to set-up, operate, and monitor CNC and/or manual Milling machines to provide operational support for the construction, assembly, and/or repair of molds, dies, and ancillary equipment. | 02/17/2025 |
| 1666 | West Exton, PA Associate Scientist Bachelor's Degree in Biology, Chemistry or a relevant scientific field preferred Exp: 0-3 years |
In this role, you will be responsible for performing testing of products for internal and external customers using a variety of analytical techniques in a QC/cGMP environment. You may be assisting in updating procedures for instrumentation, test instructions, and test reports. | 02/17/2025 |
| 1667 | Worldwide Clinical Trials San Antonio, TX Research Associate 1 Bachelor’s Degree (preferably in the field of Life Sciences or Health) Exp: 6 months |
The Research Associate 1, has have familiarity with processing and reviewing clinical documentation, interacting with participants, and accommodating competing priorities in a dynamic clinical research environment. | 02/17/2025 |
| 1668 | Worldwide Clinical Trials San Antonio, TX Senior Scientific Associate, Biomarker Analysis Bachelor’s or Master's degree Exp: 0-1 years |
As a Senior Scientific Associate in Biomarker Analysis, you will be a key contributor to our bioanalytical team. Your role involves method development, validation, and sample analysis for ligand binding assays. You’ll work closely with the supervisor to ensure accurate and efficient execution of bioanalytical processes. If you’re passionate about advancing bioanalysis research and have a strong foundation in bioanalysis, this role is for you. | 02/17/2025 |
| 1669 | WuXi AppTec Marietta, GA Associate Laboratory Technician Bachelor’s Degree Exp: 1 year |
Perform Sterility Testing in compliance with applicable Regulations, International Standards following SOPs in cleanroom type environment, perform QA/QC tasks, prep carts. | 02/17/2025 |
| 1670 | HD Biosciences (WuXi AppTec) San Diego, CA Research Associate II Bachelors in Biology related field Exp: 1-3 years |
Assisting and performing efficacy and PK-PD studies and developing new in vivo/ ex vivo assays and models with minimum supervision, as needed. Help to design, optimize and execute of pharmacology experiments for compound screening, compound mode of action and efficacy in mechanistic and disease models, e.g. syngeneic and xenograft tumor model, acute and chronic autoimmune/inflammatory conditions, and analyses and reporting of experiments or implantation, blood/tissue collection, etc. Assist with and perform other experiments as required. Working with the team to perform assay development, optimization, and validation projects. Following SOPs to perform compound receiving, registration, and management. Help to manage lab coordination. | 02/17/2025 |
| 1671 | WuXi AppTec Plainsboro, NJ Scientist I (Contingent) Master’s degree in Chemistry, Biology, or related Physical science Exp: 1-2 years |
With supervision serve as study director/principal investigator to perform MD, MV/MQ and Sample analysis for Large Molecule (LM) Bioanalysis projects. Troubleshoots Wet Lab LM Bioanalysis assays issues and assist in training of LM analysts on wet lab LM systems. Can communicate; write responses to QC/QA findings. Communicate with Clients on specific projects that they are responsible. Accountable for accurate data submission and on time delivery of assigned projects. | 02/17/2025 |
| 1672 | HD Biosciences (WuXi AppTec) San Diego, CA Research Associate II Bachelors in Biology related field. Exp: 0-1 years |
Assist with in vivo pharmacology experiments for preclinical contract research. Perform histology and immunohistochemistry work and other special stains, when needed. Schedule studies, review protocols, data and reports. Establishes scientific standards and new initiatives. Write and review SOPs. Enter data in study management software. Participates in drafting quotations. Develop, implement, optimize, and validate animal models in different disease areas. Effectively communicate with internal colleagues and external clients to promote a world-class service. | 02/17/2025 |
| 1673 | WuXi Advanced Therapies Philadelphia, PA Quality Control Environmental Monitoring Associate I Bachelor’s degree with a major in Biology, Microbiology, or related Life Science Exp: 0-3 years |
Typically, you are either supporting an operation or doing routine sampling. Routine sampling can be performed usually at any point during the day while supporting an operation will have set start and end times when the technician would have to be available. The position is 50% on your feet sampling, 25% lab work, and 25% desk work. The overall schedule tends to change on a day to day basis, this is based off of manufacturing – some of their runs are based on donor material that they don’t always have, some of the runs change based on cell counts, and some of the runs get moved around due to materials and personnel. | 02/17/2025 |
| 1674 | WuXi AppTec Philadelphia, PA Manufacturing Associate I Bachelor’s (science preferred) degree Exp: 0-2 years |
Responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 02/17/2025 |
| 1675 | Abbott Sylmar, CA Product Engineer II – Remote Care Operations Bachelor's Degree Biomedical Engineering or Science, Technology, Engineering and Mathematics (STEM) related Bachelor's degree Exp: 1-2+ years |
The Associate Remote Care Product Engineer is responsible for understanding the integrated set of standards, sub-standards, and assemblies needed to provide remote care support for Abbott CRMD devices. Applies an interdisciplinary, collaborative approach to plan, design, develop and verify a life-cycle balanced system of systems and system/subsystems solution(s) which satisfies customer/operational needs and public/regulatory acceptability. Troubleshooting complex systems and interactions with the full line of remote care capable Abbott devices and supporting hardware will be the primary focus. | 02/17/2025 |
| 1676 | Abbott St. Paul, MN Associate R&D Engineer - Clinical Engineering Bachelor's degree in Engineering (BSME or BSBME preferred) Exp: 1 year |
The Associate R&D Engineer - Clinical Engineering is responsible for evaluating new product designs and understanding how they interact with the user and patient. | 02/17/2025 |
| 1677 | Abbott Temecula, CA Associate TPM Project Engineer Bachelor’s degree in engineering, science or closely related discipline Exp: 0-3 years |
The Associate TPM Project Engineer is an engineering professional who applies scientific knowledge, engineering knowledge, mathematics, and ingenuity to complete assignments related to a specific technical field or discipline. | 02/17/2025 |
| 1678 | Abbott St. Paul, MN Development Quality Engineer II Bachelor level degree in an Engineering Discipline or other Technical Field Exp: 0-2 years |
We are seeking a high caliber Development Quality Engineer II. A development quality engineer assures new or iterative products conform to requirements and establish compliance with the quality system. This position is responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs. Each employee can make a difference at Abbott and has the power, either individually or as a team, to influence the success of the company. We are team-oriented, fast-paced and progressive. We value people with great ideas who partner with others both internally and externally to take action and accomplish goals. | 02/17/2025 |
| 1679 | Abbott Casa Grande, AZ Microbiologist - Nutrition Manufacturing Science related Bachelor’s Degree Exp: 1 year |
This position works out of our Casa Grande, Arizona location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. | 02/17/2025 |
| 1680 | Abbott Plano, TX Development Quality Engineer II Bachelor’s degree in engineering, Technical field Exp: 1-2+ years |
As the Design Quality Engineer II you will assure new or modified products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs. | 02/17/2025 |
| 1681 | Abbott Temecula, CA Quality Engineer Master's degree Exp: 0-2 years |
The Quality Engineer is expected to assist in the identification and resolution of quality related issues. You'll have the opportunity to apply subject matter expertise, in an individual contributor role with limited supervision. Expected to provide quality engineering support to the site to ensure manufacturing/quality requirements are met and understand and elevate issues related to quality validations. Work with a team to establish and implement a dynamic structure that fosters and ensures consistent compliance to external laws, regulations, guidances and standards that affect the quality system. The team will develop and follow a process to implement a structure that will facilitate a consistent implementation of external quality system standards including leading activities for site inspection readiness. This structure will improve coordination between functions and increase the awareness and compliance of external requirements. | 02/17/2025 |
| 1682 | AbbVie North Chicago, IL Associate Scientist II, Oncology Assay Lab Master’s Degree Exp: No exp |
The Oncology Discovery Research team is seeking a highly motivated and experienced Associate Scientist II with expertise in CRISPR genome editing within the Oncology Assay Lab located in Lake County, IL. This is an excellent opportunity for a cell biologist/molecular biologist to make significant contributions to the advancement of oncology drug discovery programs within a dynamic and collaborative environment. The selected individual will play a crucial role in generating high-quality drug development candidates targeting promising therapeutic areas in oncology. An important responsibility will be to investigate, identify, develop, and optimize new methods and techniques. This role will be part of a team of supporting multiple Oncology Discovery programs and projects. | 02/17/2025 |
| 1683 | AbbVie South SF, CA Associate Scientist I/II, Biologics Drug Product Development Bachelor’s degree Exp: 0-3 years |
The Biologics Drug Product Development group within AbbVie is a global organization responsible for developing and characterizing drug product formulations and manufacturing processes for biologic therapeutics (antibodies, antibody-drug conjugates (ADCs), neurotoxins, and novel biologic formats) from preclinical development through clinical proof of concept. We have an exciting opportunity available for an Associate Scientist I/II to join our team at our Bay Area site in South San Francisco, CA. This position requires an onsite presence and involves lab-based functions. Successful candidates will thrive in a collaborative lab environment. | 02/17/2025 |
| 1684 | AbbVie Westport, MO NPI QC Bioassay Trainer Bachelors or Master’s Degree of Science Exp: 1-3 years |
We are now hiring an NPI QC Bioassay Trainer into our team in Westport for a Fixed Term Contract for 23 months Fixed-Term-Contract. This person will join the Westport Bioassay department and the role centres on providing an efficient training programme to all personnel working in the QC Bioassay labs. The trainer role will be responsible for developing and managing training of all new hires for NPI QC Bioassay and will be responsible for updates to key stakeholders on training timelines to support analyst training completion on time. The trainer role will also include supporting NPI drug product stability testing, ad-hoc investigational & development testing. There may be a requirement to execute/assist on new method transfers and validations. To support this volume of testing, ancillary laboratory duties including critical reagent screening/qualifications, laboratory housekeeping, review of paperwork and procedural updates are required. | 02/17/2025 |
| 1685 | AbbVie North Chicago, IL Associate Scientist II, Analytical R&D Master’s Degree in chemistry, Analytical Chemistry, or equivalent education Exp: No exp |
For the Associate Scientist II position, we are seeking a highly motivated candidate who can independently generate precise, reliable and reproducible data in a timely manner. Can demonstrate experimental precision and strong data interpretation skills. He/she should possess understanding of core discipline and support early phase development of New Chemical Entities (NCEs) drug substance and drug product in both preclinical and clinical programs. Collaborate within the global Analytical R&D organization and with R&D cross-functional partners such as Pre-Clinical Safety (PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD), and Quality Assurance (QA) and CMC-Regulatory. | 02/17/2025 |
| 1686 | Strand Therapeutics Boston, MA Associate Scientist, In Vivo Discovery B.S. or M.S. in Biological Sciences, Bioengineering or related discipline Exp: 1-3+ years |
We are looking for an Associate Scientist to join the In Vivo Discovery group to conduct proof-of-concept, validation, and pharmacology studies to support multiple pre-clinical programs. You will be passionate about scientific discovery, undeterred by bold challenges, and enjoy working as a team to develop the next generation of mRNA medicines. You should be highly organized, a critical thinker, adaptable to changing priorities, and possess a strong ability to collaborate effectively with teams of diverse backgrounds. | 02/11/2025 |
| 1687 | Sun Pharma Billerica, MA Process Development Scientist I BS in related scientific major Exp: 1-3 years |
Provides support for new product formulation, aseptic & topical process development, process transfers and troubleshooting existing manufacturing processes. | 02/11/2025 |
| 1688 | SBI Palo Alto, CA Technical Support Specialist (TSS) Master's in a life sciences field (Molecular Biology, Cell Biology, Biotechnology, or a related field) Exp: 1-2 years |
As a Technical Support Specialist, you'll play a critical role in empowering researchers worldwide. You'll work closely with scientists to provide expert guidance, troubleshoot technical issues, and contribute to product development. | 02/11/2025 |
| 1689 | SystImmune Inc Redmond, WA Research Associate/Senior Research Associate BS or MS in immunology, biochemistry, molecular biology, structural biology, or a related field Exp: 1+ year |
We are seeking a skilled Research Associate/Senior Research Associate with experience in utilizing display technologies (yeast/phage) in protein engineering, directed evolution, or binder discovery. This is a laboratory-based role that will be supporting protein engineering efforts in discovering novel binders and novel protein leads/scaffolds. The position will join a growing protein engineering team in an innovative organization and reports to the Director of Protein Engineering. The ideal candidate will be a quick learner with a broad experience set with direct expertise in a display technology and/or an adjacent field including but not limited to high throughput molecular biology, antibody/binder discovery, and protein engineering. Industry experience in biologics drug development is required. | 02/11/2025 |
| 1690 | SystImmune Inc Redmond, WA Research Associate/Senior Research Associate - Cell Science Bachelor’s degree in biology or a related science major Exp: 1+ year |
We are seeking a Research Associate / Senior Research Associate with experience in cell culture and plasmid preparation to join our Cell Science Department. | 02/11/2025 |
| 1691 | Takeda Boston, MA Senior Research Associate - Binding MS in scientific discipline Exp: 1+ years |
The Global Biologics Biological Generation and Analytics team seeks an enthusiastic, energetic, and team-oriented individual to join us. The position involves contributing to the team by identifying binding interactions through various techniques and independently analyzing data. Responsibilities include designing and executing experiments, troubleshooting as needed, and actively participating in program teams to develop analytical strategies. Effective communication skills and the ability to work within cross-functional teams are essential. | 02/11/2025 |
| 1692 | Takeda Boston, MA Research Senior Associate, Inflammation (GI2) Drug Discovery MS in a scientific discipline Exp: 1+ years |
The Gastrointestinal and Inflammation (GI2) Drug Discovery Unit at Takeda is building a new team of experienced, innovative, and collaborative researchers to deliver an industry-leading portfolio of drugs for various gastrointestinal, autoimmune, and inflammatory diseases with high unmet medical needs. We seek a skilled Research Senior Associate to join our biology and cross-functional discovery teams and create novel drug candidates. | 02/11/2025 |
| 1693 | Takeda Thousand OAks, CA Quality Analyst Bachelor’s degree in chemistry or Biological Sciences Exp: 1 year |
The Quality Analyst will be responsible performing the daily quality operations for Quality Lab Services within the Quality organization. You will manage stability management, basic investigation activities, coordinating external lab testing, managing analytical instrument preventive maintenance, inventory management, compiling critical quality attributes data for the Product Quality review and Yearly Biologic Product Report, initiating deviations, and participating in quality process improvements for the QC labs. You will report to the AQC Manager. | 02/11/2025 |
| 1694 | Takeda Brooklyn Park, MN Development Associate II Master’s degree in a scientific discipline Exp: 0-3 years |
As a Development Associate II, you will work with other members of the Technical Operations group to lead tech transfers of products into the facility at bench and pilot scale and subsequently to commercial scale. You will provide manufacturing technical support including batch records, deviations, change controls, investigations, life cycle management, scale down modeling, satellite runs, process validation, data tracking and trending, and supporting CMC regulatory filings. You will report to the Senior Manager of Technical Operations. | 02/11/2025 |
| 1695 | Takeda Boston, MA Research Senior Associate, Oncology Drug Discovery Unit MS in a scientific discipline (or equivalent) Exp: 1+ years |
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Research Senior Associate, Oncology Drug Discovery Unit in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. | 02/11/2025 |
| 1696 | Takeda Cambridge, MA Research Associate, Binding and Characterization MS or BS degree in scientific discipline Exp: 1 year |
The Global Biologics Biological Generation and Analytics team seeks an enthusiastic, energetic, and team-oriented individual to join us. The position requires technical understanding of binding interactions and instrumentation used for binding, BLI and SPR. Individual will be responsible for understanding and interpreting data generated. The individual will be required to work with peers to design and implement binding experiments. This position requires the ability to perform in team setting. | 02/11/2025 |
| 1697 | Tanvex San Diego, CA QC Associate, Quality BS or advanced degree in chemistry, biology, biochemistry or related life sciences discipline Exp: No Exp |
The Quality Control Associate I, is responsible for supporting the control and management of samples within QC and performing routine testing of in-process, release, and stability samples following written methods and procedures. The position will work as part of the Analytical Development (AD) / Quality Control (QC) group to support the team responsibilities. Adherence to GMP/ GDP guidelines and ability to follow SOP’s is required. | 02/11/2025 |
| 1698 | TE Connectivity Atlanta, GA Staff Field Application Engineer Bachelor’s Engineering Degree in one of the academic discipline's mechanics, electrics, electronics Exp: 1-3 years |
TE Connectivity’s Field Application Engineering Teams work intimately with customers to recommend products and solutions for new and existing applications. They identify new applications, requirement modifications and enhancements to meet customer specifications and conduct on-site installation and service of product and are responsible for all technical aspects of the sales cycle for potential application of company products to meet customer needs, including identifying opportunities; determining solutions; creating demand; preparing detailed product specifications and technical marketing support; ensuring high quality and timely project execution and conducting follow-up technical support. They also approve operational quality of systems and equipment. | 02/11/2025 |
| 1699 | TE Connectivity Middletown, PA R&D/Product DVL Engineer I BA/BS degree or higher in mechanical engineering Exp: 0-3 years |
TE Connectivity’s R&D/Product Development Engineering Teams conceive original ideas for new products, introduce them into practice. They are responsible for product development, and qualification from market definition through production and release; assist in the qualification of suppliers for new products to ensure suppliers deliver quality parts, materials, and services for new or improved manufacturing processes; conduct feasibility studies, testing on new and modified designs; direct and support detailed design, testing, prototype fabrication and manufacturing ramp. The R&D/Product Development Engineering Teams provide all required product documentation including, but not limited to, Solid Model, 2D/3D production drawings, product specifications, and testing requirements. They create and modify detailed drawings and drafting or conceptual models from layouts, rough sketches or notes and contribute to design modifications to facilitate manufacturing operation or quality of product. Typical fields of expertise include: materials, mechanics and systems, electrical, optics, chemistry, software, automation systems, packaging, testing and measurement, and manufacturing of electrical, mechanical and electronic components, products, and their integration into systems. | 02/11/2025 |
| 1700 | TE Connectivity Mansfield, OH Research & Development Product Development Engineer II Bachelor’s Degree in Engineering, E.E. Exp: 1-5 years |
The R&D/Product Development Engineering is responsible for the design, development of product line extensions of legacy product, with a focus on sustaining engineering of contactors/relays, power distribution panels and related products for applications in aerospace electrical power distribution and management systems. The ideal candidate should be able to work independently and within a team-based environment. Determine product requirements based on internal/external product design specifications and Voice of the Customer inputs. Plan and record results of design, development, and sustaining activities, including validation testing. Design to cost target while meeting financial and performance expectations. Manage Bill of Materials for products. Facilitate cost reduction activities on new and existing products. Perform calculations, analysis, and testing to ensure that a product meets specifications. Participate in and/or lead Design and Process failure mode and effects analysis. Provide support to both internal manufacturing, quality, Product/Project Managers, and external customers. Initiate and manage engineering change activities. Apply electrical, electronic, and mechanical principles to components, including assembly, analysis, and documentation of results. Supports, participates, and leads design, test, modification, fabrication, and assembly of prototype devices. | 02/11/2025 |
| 1701 | Tempus Durham, NC Molecular Technologist I-IV BS/BA or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 02/11/2025 |
| 1702 | Tempus Chicago, IL Quality Control Technologist I-III BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work within a cutting-edge genomics workflow to provide quality control support in a high-volume clinical molecular laboratory. Help create and implement new equipment functionality for use by Tempus R&D and clinical lab staff while maintaining CLIA/CAP/NYS-DOH/ISO compliance. Test and document new lots of reagents for clinical lab team processing and label reagents approved for use. Maintain reagent qualification records and manage quality control of reagent inventory. Collect and help analyze metrics. Complete Performance Qualifications (PQs), Preventive Maintenance (PM), relocation, and routine maintenance for all clinically approved molecular laboratory equipment. Investigate issues and help facilitate and implement corrective and preventative actions. | 02/11/2025 |
| 1703 | Tempus Chicago, IL Research Associate BS or MS degree in Immuno Oncology, Cellular or Molecular Biology or related field Exp: 1-2+ years |
We are looking for a highly skilled Research Associate to join our Biological Modeling team within the Biorepository. Our CAP accredited Biorepository develops complex, microenvironment-rich human tumor models for use in a range of studies with our academic and pharmaceutical partners to develop next generation cancer therapies. The ideal candidate will have a strong understanding of immuno-oncology, cell biology and experience with sterile tissue culture and molecular techniques. Prior laboratory experience with mouse and human primary cells and training in CRISPR gene editing approaches is preferable. The successful candidate will be responsible for developing, maintaining and archiving tumor organoid cultures, as well as working with multidisciplinary teams supporting functional assays. | 02/11/2025 |
| 1704 | Tempus Chicago, IL Molecular Technologist I-IV BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 02/11/2025 |
| 1705 | Tempus Chicago, IL Molecular Technologist (Wed-Sat PM Shift) BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 02/11/2025 |
| 1706 | Tempus Chicago, IL Molecular Technologist I-II (3rd Shift) BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 02/11/2025 |
| 1707 | Tenaya Therapeutics Union City, CA QC Analyst (Contract) Bachelor’s or master’s degree in biology, Biochemistry, or a related field Exp: 6 months |
In this role, you will support QC GMP operation and key assays for release, in-process, and stability testing; Other activities include but not limited to data trending, archiving, lab/equipment maintenance, reagent preparation/supplies ordering, supporting EM and microbiology testing. Final job title will be determined based on candidate experience level. | 02/11/2025 |
| 1708 | Terumo Medical Corporation Elkton, MD Quality Engineer I Bachelors degree in engineering, engineering technology, computer science, mathematics, or physics Exp: 1 year |
The position as a Quality Engineer will work closely with the Operations and Engineering Teams to ensure that goods and current products are well designed and manufactured to meet or exceed the customer expectations and requirements. This position will support manufacturing production and is responsible for performing corrective actions and driving continuous improvement initiatives. Ensure compliance to Terumos quality policy, respond to customer complaints, perform audits, develop test methods, and/or write procedures for material characterization. | 02/11/2025 |
| 1709 | Tessera Therapeutics Somerville, MA Research Associate I, High Throughput Oligonucleotide Chemistry BS/MS degree in Chemistry, Biology or related field Exp: 0-1 year |
Tessera Therapeutics is looking a Research Associate to support upstream processes for Oligonucleotide manufacturing, research and scale -up. You are interested in gaining a deep understanding of organic synthesis techniques and finding efficient ways to synthesize long oligonucleotide. You are comfortable multitasking in a fast paced environment under supervision with support of your team on various aspects of the platform. You are an independent, creative thinker with high attention to detail and are enthusiastic about contributing to new ideas. | 02/11/2025 |
| 1710 | Tessera Therapeutics Somerville, MA Research Associate II/Senior Research Associate, Oligonucleotide Foundry MS in chemistry, biology, or related life sciences Exp: 1+ years |
Learning and implementing purification strategies for complex oligonucleotides. Conducting research into alternate purification strategies. Preparing transfer of methods to larger-scale cGMP manufacturing environment. Performing routine operations for critical technology components. Participating in cross-functional teams and training to gain familiarity in all stages of oligonucleotide research and manufacturing | 02/11/2025 |
| 1711 | Tevard Biosciences Cambridge, MA Research Associate, in vivo pharmacology BS/MS in Neuroscience, Physiology, Molecular/Cellular Biology, or a related Life Science discipline Exp: 0-2 years |
We are looking for Research Associate (RA-I or RA-II) with an innovative mindset, great attention to detail and ability to work collaboratively to solve problems, to help advance therapeutic candidates to the clinic. The successful candidate will have an opportunity to positively impact patients with serious unmet medical needs while working closely with our world-class scientific team, including with company’s scientific co-founders In this position, you will collaborate with the in vivo pharmacology team to study effects of therapeutic lead candidates. The RA will work with animal models for rare genetic diseases and will be responsible for executing experiments to quantify molecular, cellular, and physiological readouts, in addition to supporting in vivo dosing studies and related research activities within the in vivo pharmacology group. This is an exciting opportunity for a motivated scientist to further develop their skills in neuroscience, physiology and gene therapy while helping to make an impact on lives of patients suffering from rare diseases. | 02/11/2025 |
| 1712 | Ritedose Columbia, SC Microbiologist I B.S. degree in Microbiology or related field. Exp: 0-1 years |
The Microbiologist I is responsible for all duties related to performing environmental monitoring, personnel monitoring, microbial enumeration, microbial identification, and sampling of utilities. The Microbiologist I is also responsible for performing all the microbiological testing related to raw materials, utilities, and in-process product testing. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining and ordering inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. | 02/11/2025 |
| 1713 | Theradex Oncology Princeton, NJ Clinical Research Associate I Bachelor's degree in biological or human science-related field Exp: 1 year |
At Theradex, you aren’t just a number. You are part of a highly engaged team of exceptional and supportive people who pride themselves on quality monitoring, continuous learning, challenge themselves and who reap the rewards of providing first in class monitoring to our sponsors. | 02/11/2025 |
| 1714 | Theragenics Buford, GA Process Engineer Bachelor’s degree in engineering, Life Sciences, or a related technical field Exp: 1-3 years |
The Process Engineer is essential to ensuring the seamless integration of manufacturing processes with quality management systems, driving operational efficiency, product excellence, and regulatory compliance. This role combines process engineering expertise to optimize production workflows and resolve technical challenges with quality engineering responsibilities, including maintaining product quality, managing non-conformances, and supporting continuous improvement efforts. This individual is responsible for supporting the development and implementation of robust procedures, track key performance indicators, and ensure alignment with industry standards. A successful Process Engineer will bring strong problem-solving skills, a data-driven mindset, and a proactive approach to identifying and implementing process improvements. | 02/11/2025 |
| 1715 | Thermofisher Worcester, MA Labs FSP Associate Scientist - Separations and Automation Technologies Bachelor's degree in biological or human science-related field Exp: 0-2 years |
In this position as an Associate Scientist, you should possess a thorough understanding of laboratory procedures. You will perform a variety of complex sample preparation and analysis procedures to quantitatively measure biopharmaceutical compounds in a variety of biological matrices. Instrumentation is primarily HPLC and CE. Hamilton Liquid Handlers Protein Maker affinity purification is used as well. Requires following analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against acceptance criteria, methodology, protocol and product specifications. Enters data into databases and reports. | 02/11/2025 |
| 1716 | Thermofisher Cincinnati, OH Quality Specialist II (GMP Investigations) Bachelors Degree in Chemistry, Biology, Engineering or relevant science Exp: 1+ years |
Investigates and observes Operations and Quality Operations departments to assure that FDA current Good Manufacturing Practices, company SOPs and product registrations are followed and maintained. Conducts investigations of batches, preps, lots, equipment, and facilities in accordance with the Code of Federal Regulations. Assists the Operations and Quality Operations departments in satisfying all FDA and DEA requirements. | 02/11/2025 |
| 1717 | Thermofisher Cincinnati, OH Engineer II, Manufacturing Engineering Bachelor’s Degree in Industrial, Manufacturing, Chemical, Mechanical engineering or related field Exp: 1 year |
This role will support manufacturing production through root cause analysis and implementing engineering solutions. The Engineer will identify and complete improvements to current manufacturing processes. Must uses the latest engineering techniques to reduce product time to market whilst adhering to regulatory requirements, project timelines and product costs. | 02/11/2025 |
| 1718 | Thermofisher Middleton, WI Entry Level Scientist (Scientist I) Bachelor's degree (Life Sciences degree preferred) or equivalent Exp: 0-2 years |
As a Scientist I, you will use innovative technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and analysis serve as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. | 02/11/2025 |
| 1719 | Thermofisher Middleton, WI Associate Group Leader - Cell Lab Bachelors degree Exp: 1+ year |
Provides line-level management coordination of resources and work schedules for laboratory activities. Oversees daily operations and assists in preparation and implementation of company policies, quality systems and training programs. Ensures that projects are completed in a timely manner so that company revenues are met and clients are satisfied with the quality and turnaround time of work being performed. Ensures that laboratory staff continues to be developed to keep pace with department goals and growth. | 02/11/2025 |
| 1720 | Thermofisher Richmond, VA Assistant Scientist Bachelor's degree Exp: 0-1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 02/11/2025 |
| 1721 | Thermofisher Middleton, WI Formulation Tech II (High Volume) - 2nd Shift B.S. in Science or Medical Technology Exp: 1 year |
Join Thermo Fisher Scientific as a Large Volume Formulation Tech 2 on our 2nd shift. This position in our Manufacturing division offers a remarkable chance to perform precise techniques and procedures in formulating liquid chemical solutions for reagents, controls, and calibrators. You will work with large volume equipment (1500L – 36000L). | 02/11/2025 |
| 1722 | Tolmar Windsor, CO Manufacturing Operations Engineer I Bachelor’s degree in engineering or similar field Exp: 1+ years |
The Manufacturing Operations Engineer I provides technical support for manufacturing processes for specialty injectable and aseptic products while ensuring those products are made with quality for our patients. The Manufacturing Operations Engineer I assists with protocols and changes for the Manufacturing Department and provides hand-on and technical support for other department projects when dealing with Manufacturing. Owns Quality Event investigations and supports equipment troubleshooting / updating / installing. Manufacturing Operations Engineers are system owners for the Electronic Batch Records (EBR) and Freeweigh systems and serve as the manufacturing technical point of contact for Enterprise Resource Planning (ERP) projects. | 02/11/2025 |
| 1723 | Tolmar Windsor, CO MS&T Engineering Technician (Temporary) BS/MS in scientific or engineering field Exp: 1+ years |
Under general supervision, provides office and laboratory support to the Technical Services group in the MS&T department, which includes a variety of technical documentation activities, administrative activities, product investigation activities, and related tasks. | 02/11/2025 |
| 1724 | Transpire Bio Miami , FL Associate Scientist I/II BSc or MSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct laboratory activities with limited supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all testing performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of inhalation drug product. Prepare samples for blend uniformity. Perform equipment qualification and calibrations as directed. | 02/11/2025 |
| 1725 | Trinity Waltham, MA Research Associate - Value, Access, and Pricing (EVAP) Bachelor’s degree or master’s degree in life sciences Exp: 1-3 years |
We are currently seeking a Research Associate to support Trinity’s Evidence, Value, Access, and Pricing (EVAP) teams with research activities spanning several adjacent areas: Payer / HTA and pricing analysis, life science-related landscape research, targeted and systematic literature review, and research relating to value dossier development. | 02/11/2025 |
| 1726 | SGS Deer Park, TX Chemist Bachelor’s Degree in Chemistry or a related science Exp: 1 year |
Responsible for analysis and reporting of various products such as crude oil, fuel oils, middle distillates, petroleum and petrochemicals, LPG & LNG gases, etc. | 02/05/2025 |
| 1727 | Sharp Packaging Services Allentown, PA Quality Specialist (2nd shift) Bachelor’s degree Exp: 1-3 year |
The Quality Specialist provides quality oversight, GMP guidance and support and makes quality related decisions for the designated functional areas within Sharp Commercial sites. They work closely with internal teams daily and occasionally represent Sharp Quality in customer interactions. The Quality Specialist is responsible to support, design and implement GMP initiatives and continuous improvement opportunities within the Quality Operations organization through data analysis, training, motivation and coaching in collaboration with internal and external stakeholders. Must possess a working knowledge of FDA regulations pertaining to Pharmaceutical /Pharmaceutical Packaging Operations. | 02/05/2025 |
| 1728 | Shennon Biotechnologies San Francisco, CA Research Associate Bachelor’s degree in Molecular Biology, Biology, Biochemistry, Biomedical Engineering or equivalent Exp: 1-3 years |
We are a well-funded early-stage startup based in SF that has created a proprietary single cell platform for the development of more effective cancer immunotherapies. We are looking for a research associate to join our interdisciplinary team. The candidate is expected to learn quickly and communicate well, especially in a fast-paced startup environment. The candidate will work directly with all members of the team. The ideal profile is someone who wants to gain a few years of research experience before going back to graduate school or someone who has just finished college/master's and wants to support scientists in the long term. | 02/05/2025 |
| 1729 | SHL Medical Deerfield Beach, FL AS Engineer B.E. in Biomedical Engineering/Mechanical Engineering or any relevant branch of study. Exp: 0-2 years |
Execute tests, document & analyze test data, write protocols, procedures, equipment work instructions, test instructions. | 02/05/2025 |
| 1730 | Siegfried Grafton, WI Process Engineer Bachelor's degree in Chemical Engineering Exp: 0-5 years |
The incumbent manages all technical aspects of assigned products and/or new processes in manufacturing. This includes preparing batch log records and cleaning log records, supporting production, conducting investigations, implementing corrective actions, and improving yields and cycle times. | 02/05/2025 |
| 1731 | Siemens Charlotte, NC Smart Buildings Associate Energy Engineer Bachelor’s degree in Engineering or related technical field Exp: Entry Level |
The Associate Energy Engineer primary responsibility is driving growth in our Energy Services business by performing and supervising facility site visits/audits, analyzing the customer’s current situation, and developing Facility Improvement Measures (FIMs). This position works closely with Sales in the identification and qualification of Energy Services projects and supports ongoing service agreements. | 02/05/2025 |
| 1732 | Siemens Healthineers Mishawaka, IN Scientist I Bachelor of Science (BSc) or Masters (MS) degree in Chemistry or Organic Chemistry Exp: 1-3 years |
Analyzes and designs work systems in order to support general adherence to agreed standards, in order to ensure humanely and economical production and drives continuous improvement topics. This is a preparative organic chemistry synthesis position at the Siemens Healthcare Diagnostics Mishawaka, Indiana facility; Organic Chemistry Group (OCG). The position requires 70% lab/bench work and 30% office/documentation. ‘Work from home’ is NOT an option for this position. The normal work week is 40 hours. However, additional time may be required to meet specific product delivery and chemistry demands. | 02/05/2025 |
| 1733 | Revvity Remote, PA Associate Customer Service Engineer B.S in Physics or Engineering discipline Exp: 0-2 years |
Revvity is seeking a Customer Support Engineer to join a customer focused field service team in our High Content Imaging Business Unit for the Mid-Atlantic territory (PA, NY & NJ regions). The High Content Imaging Business Unit focuses on the sales of Opera Phenix Plus and the Operetta CLS and related products. The successful individual will provide field service support for the continuously growing High Content Imaging install base in the United States including installations, training, customer training, preventative maintenance, and repair. The individual will also assist with technical support to end-users and field service engineers. | 02/05/2025 |
| 1734 | Revvity San Diego, CA Biochemist I - Bacterial Cell Culture Bachelor of Science in Life Science Exp: 6+ months |
Join our dynamic Molecular Cellular Immunology (MCI) team as a Recombinant Manufacturing Associate, where you’ll play a pivotal role in creating groundbreaking recombinant protein research products. In this hands-on position, you'll be involved in every step of the production process, from recombinant protein expression to purification. Your expertise will be key in tasks like preparing buffer solutions and cell culture media, performing bacterial cultures, and using cutting-edge techniques to affinity purify recombinant proteins. You'll also be responsible for DNA isolation in accordance with established protocols. This role offers exciting opportunities to expand your skill set, with potential additional responsibilities including transferring products to other teams for testing, preparing detailed product and project documentation, and managing inventory and records for recombinant protein products. | 02/05/2025 |
| 1735 | Revvity San Diego, CA Biochemist I - Purification Bachelor’s of science degree in biology, biochemistry, chemistry, or other related area Exp: 1 year |
The Biochemist I will be an integral member of a team that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform antibody purification via column chromatography both manually and automatically, troubleshooting of problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 02/05/2025 |
| 1736 | Revvity San Diego, CA Research Associate II - Product Development Bachelor’s Degree in life sciences Exp: 6+ months |
At BioLegend (a division of Revvity, Inc.) we develop novel, cutting edge products and offer custom services to help with scientific innovation and discovery. We are currently looking for a talented, detail oriented person to join our growing Product Development team. The potential candidate will assist with development of new products for cell analysis such as antibodies, multi-color panels, and reagents for analysis of cell metabolism and cell imaging. The successful candidate must be a self-motivated, team player, able to communicate effectively with a multi-disciplinary team and must possess excellent organization skills. | 02/05/2025 |
| 1737 | Revvity San Diego, CA R&D Materials Coordinator B.S. in Biology, or other biological field Exp: 1-2 years |
Are you ready to kickstart your career in the exciting world of biotech? We’re looking for a motivated and detail-oriented Material Coordinator to join our team! This on-site, entry-level position plays a key role in supporting our corporate business development efforts as we expand our product portfolio through in-licensing, in-house development, and strategic acquisitions. As a Material Coordinator, you’ll be at the heart of our operations, managing the flow of incoming materials. From documenting and receiving to distributing materials to internal stakeholders and external locations, your contributions will directly impact the success of our business. You’ll also work closely with cross-functional teams across Finance, Customer Service, Research and Development, Purchasing, Facilities, and Quality Assurance—making it a truly collaborative experience. This role offers the perfect blend of Biology and Business, providing you with a unique opportunity to learn the ropes of biotech research and development while helping drive forward our company's growth. | 02/05/2025 |
| 1738 | Revvity Lafeyette, CO Associate Scientist- Molecular Biology Bachelor’s Degree in life or natural sciences Exp: 0-2 years |
Revvity has an exciting opportunity for an enthusiastic Associate Scientist for molecular biology/viral production. The Associate Scientist position will perform primary tasks in an ISO 9001:2015 biology manufacturing laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the processing and preparation RNAi and Gene Editing products including molecular biology bench work, cloning, viral production, nucleic acid purification, collection replication, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of molecular biology and microbiology. | 02/05/2025 |
| 1739 | Revvity Lafeyette, CO Scientific Support Specialist - Hybrid MS in Biological Sciences. Exp: 1-2+ years |
The Scientific Support Specialist helps researchers achieve cutting edge scientific results by providing timely, high-quality support to customers using our full portfolio including Dharmacon brand gene editing, RNAi, cell culture, gene expression & companion diagnostic products. Working as part of our highly experienced technical team, the Scientific Support Specialist will use their scientific expertise daily to guide customers through their full experimental journey: Addressing pre-sales questions and inquiries, troubleshooting problems, and managing complaints in a fast-paced and dynamic work environment. Through in-depth interactions across the company, this role will provide extensive insight into the business world and would be a perfect introduction to the commercial sector for an applicant interested in applying and sharing their scientific knowledge. The position will be ultimately based in our offices either in Lafayette, CO, or Cambridge, UK on a hybrid basis. | 02/05/2025 |
| 1740 | Smithers Darien, IL Associate Chemist I B.S. degree in chemistry or related field Exp: 6 months |
The Associate Chemist I performs critical sample processing and extraction duties to prepare cannabis samples for analysis. The Associate Chemist I enters sample information in the laboratory information management system (LIMS) to facilitate subsequent analysis. The position is responsible for maintenance of laboratory stock reagents. Operates and may maintain, under supervision, test equipment and apparatus. | 02/05/2025 |
| 1741 | Smithers Gaithersburg, MD Associate Scientist- Molecular Biology BA/BS in Biological or Physical Sciences Exp: 6 months |
Smithers PDS LLC (Pharmaceutical Development Services) offers a comprehensive range of pre-clinical and clinical services for all phases of drug development, including support for development of drug delivery devices, and medical and pharmaceutical packaging testing. Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories. We are seeking a talented Associate Scientist to join our team in the Gaithersburg, MD laboratory. | 02/05/2025 |
| 1742 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field Exp: 6 months |
Performs a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 02/05/2025 |
| 1743 | Smithers Gaithersburg, MD Scientist I MS in biology, life sciences, or chemistry field Exp: 1 year |
Smithers PDS is seeking a Scientist to join our team in Gaithersburg, MD. The Scientist performs data analysis and various assays according to SOP with reliability while applying and meeting GLP, GCP, and/or CLIA requirements. This position assists with ensuring that the lab, materials, and equipment are maintained. | 02/05/2025 |
| 1744 | Smithers Wareham, MA Associate Chemist B.S. degree in chemistry or related field Exp: 6 months |
Smithers Cannabis Testing Services division is seeking an Associate Chemist I at our Wareham, MA location. Essential Functions: Cannabis sample processing of flower, concentrates, extracts, and infused products. Cannabis sample extraction & dilutions. Routine maintenance of laboratory equipment and instrument calibration. Wash glassware used by the laboratory. Accurate entry of sample data into LIMS. Production of laboratory reagents and stocks. Additional duties as assigned. | 02/05/2025 |
| 1745 | Smithers Warwick, NY Associate Scientist- Molecular Biology Bachelor’s degree in the chemical, environmental, physical or biological sciences, or engineering Exp: 0-1 years |
The Cannabis Lab Associate Scientist plays a key role in laboratory operations, ensuring accurate and timely handling of cannabis samples for testing. This position is responsible for assisting with sample intake, weighing and preparing samples, and performing physical chemistry tests to support quality control and compliance. Ideal candidates are detail-oriented, possess a strong foundation in laboratory practices, and are committed to maintaining high standards of accuracy and precision. | 02/05/2025 |
| 1746 | Sofie Miami, FL Quality Assurance Specialist (QAS) I Bachelor’s Degree (Scientific / Medical / Quality) Exp: 1-2 years |
The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. | 02/05/2025 |
| 1747 | Sofie Albany, NY Quality Assurance Specialist I Bachelor’s Degree (Scientific / Medical / Quality) Exp: 1-2 years |
The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. | 02/05/2025 |
| 1748 | Sofie Somerset, NJ Quality Assurance Specialist I Bachelor’s Degree (Scientific / Medical / Quality) Exp: 1-2 years |
The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. | 02/05/2025 |
| 1749 | Sofie Decatur, IL Quality Assurance Specialist I Bachelor’s Degree (Scientific / Medical / Quality) Exp: 1-2 years |
The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. | 02/05/2025 |
| 1750 | Sonosite (Fujifilm) Bothell, WA Regulatory Affairs Associate Bachelor’s degree Exp: 1-2 years |
The Regulatory Affairs Associate requires application of regulatory knowledge and project management skills to oversee international registration of new products. As the Regulatory Affairs Associate, you will also work with Regulatory team members & international teams to drive systems & process improvement activities for integrated regulatory compliance and global submission processes, including labelling, clinical affairs, new product development, international regulatory requirements and other areas as assigned. | 02/05/2025 |
| 1751 | Hologic Marlborough, MA Quality Assurance Engineer 1 - Chemical Compliance Bachelor’s degree in Chemical Engineering or Scientific field preferred Exp: 1+ years |
The Chemical Compliance Quality Specialist is responsible for developing, implementing, and maintaining Quality Management System (QMS) procedures and work instructions related to chemical compliance within the division. This role serves as a liaison between the Corporate Chemical Compliance group and the division, ensuring regulatory and QMS changes are assessed and implemented. The specialist leads the quarterly Chemical Compliance review process, monitors Key Process Indicators (KPIs), and supports product development and engineering teams as a Subject Matter Expert. Additionally, this position involves assessing product compliance, reviewing engineering changes, conducting production record reviews, and performing investigations. | 02/05/2025 |
| 1752 | Southern Biotech Birmingham, AL Quality Control Technician Bachelor’s Degree in Science Exp: 1 year |
We are currently seeking a Quality Control Technician for testing products, such as antibodies and proteins, following SOP’s and ISO requirements. | 02/05/2025 |
| 1753 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist I BA/BS Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 02/05/2025 |
| 1754 | SRI Ann Arbor, MI Research Engineer / Scientist MS in Oceanography, Geophysics, Applied Math, Physics, or Engineering (e.g. ME, Civil, Aero) Exp: 0-5 years |
We are looking for a Research Engineer or Scientist to work as part of an interdisciplinary team on ocean modeling and exploitation of sensor data in an oceanographic context. This position will be on site in Ann Arbor, MI with flexibility for a hybrid work schedule, 2 days on site and 3 days working from a home office. | 02/05/2025 |
| 1755 | Staar Surgical Tustin, CA Product Development Engineer B.S. or Master's in Engineering or Science discipline. Exp: 1-2 years |
Performs activities associated with the development of new ophthalmic lenses and delivery systems and supports existing products and processes in accordance with Design Control procedures. Develops product specifications, manufacturing methods and procedures under supervision. Conducts test protocols, verification and validation activities, and equipment qualifications under supervision. Prepares test protocols and reports, verification and validation reports, and equipment qualification protocols under supervision. Responsible for producing product development documentation in accordance with Good Documentation Practice. Assists in product conceptualization and design and feasibility testing. Documents work in laboratory notebooks and Technical Reports. Other duties as assigned | 02/05/2025 |
| 1756 | Standard Biotools Boulder, CO Quality Control Analyst I Bachelor’s Degree – major in Chemistry, Biology, or related science Exp: 1-5 years |
We are currently looking for a Quality Control Analyst to perform analysis of raw materials, finished product, stability samples, and R&D materials as part of the quality team. This will include understanding the basics of proteomics and DNA, handing sensitive materials, performing statistical analysis on results, and technical writing to report results as part of supporting multiple departments to achieve a common goal | 02/05/2025 |
| 1757 | Starkey Eden Prairie, MN Firmware Engineer II MS in Electrical Engineering or related field Exp: 1+ years |
The primary objective of the firmware engineering position is to apply their knowledge of embedded systems, digital signal processing, and wireless communications to create, test, and maintain firmware for hearing aid and accessory products. As a member of the firmware engineering department firmware engineers operate in the scope of New Product Development Projects and Advanced Development Projects. They engage regularly with other product development teams to deliver high quality and on-time hearing products to the market. A firmware engineer works under general supervision; developing and communicating solutions to routine technical problems of ample scope. They contribute to the completion of detailed technical tasks. Failure to achieve the desired results can be overcome but may cause delays in program schedules. | 02/05/2025 |
| 1758 | Starkey Eden Prairie, MN Electrical Engineer II - Electroacoustic Engineering Master of Science in Electrical Engineering or related field Exp: 1 year |
The Electrical Engineer II, under general supervision, are responsible for the design of new products and ensuring that they meet performance, quality, manufacturing, and cost requirements for Standard (Behind the Ear - BTE) and/or Custom (In the Ear - ITE) products. Must possess communication ability, technical expertise, creativity, and internal drive to lead the creation of designs that are recognized as best- in-class in the hearing aid industry. Must be able to work well in a team environment and have a passion for continuous improvement. | 02/05/2025 |
| 1759 | STERIS Hauppauge, NY Technical Support Specialist - Software 1 Bachelors degree in one of the related fields: Engineering, Audio/Video, Computer Science, MIS, CIS or related field Exp: 1 year |
As a Technical Support Specialist- Software Integration you will provide technical support to Customers, Partners and the Field Service Team to drive complete resolution of first response and moderately complex issues, along with providing Part Identification assistance. You will be expected to quickly address all incoming inquires delivering timely “service by phone” while delivering an overall extraordinary Customer experience. You must manage the situation to de-escalate while resolving the issue(s). As a specialist you will leverage remote diagnostics, your experience with the products, understanding of the theory of operation/safety hazards for the products and troubleshooting experience to resolve issues quickly. Inquires may include troubleshooting and corrective maintenance advice related to controls, electrical, IT/software, and electronics issues. You will refer complex issues to Product Support Specialists and Senior Service Engineering staff. | 02/05/2025 |
| 1760 | STERIS Spartanburg, SC Quality Analyst Bachelor's Degree in Science or Other Technology Exp: 1-5 years |
The Quality Analyst is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. Responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting. | 02/05/2025 |
| 1761 | STERIS Mentor, OH Lab Based Quality Engineer Bachelor’s Degree (Engineering or related technical field) Exp: 1 year |
Lab-based Quality Engineer dedicated to conducting testing, data mining, data analysis, monitoring, test method development, etc. in support of sustaining product investigations in collaboration with Quality Engineering and R&D teams. Develops and implements methods and procedures for process control, process improvement, testing and inspection to ensure that the products are free of flaws and function as designed. Performs product testing and analysis to maintain quality levels and minimize defects and failure rates. Analyzes reports and defective products to determine trends and recommend corrective actions. | 02/05/2025 |
| 1762 | STERIS Conroe, TX Quality Engineer Bachelor’s Degree Engineering or related technical field. Exp: 1+ years |
The Quality Engineer in our Conroe, Texas facility is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. In this role the Quality Engineer supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 02/05/2025 |
| 1763 | STERIS Sharon Hill, PA Quality Systems Engineer Bachelor's Degree in Engineering General or Other Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. This position is located in the greater Philadelphia area. | 02/05/2025 |
| 1764 | STERIS Brooklyn Park, MN Quality Analyst Bachelor’s degree in scientific or technical field. Exp: 1-5 years |
At STERIS, the Quality Analyst is responsible for assisting in administration of the quality management system at our Minneapolis site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. You will be responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting. | 02/05/2025 |
| 1765 | STERIS Minneapolis, MN Quality Analyst Bachelor’s Degree (Scientific or related technical field) Exp: 1-5 years |
The Quality Analyst is responsible for assisting in administration of the quality management system at our Minneapolis site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. You will be responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting. | 02/05/2025 |
| 1766 | Regeneron Tarrytown, NY Process Development Engineer I, Purification Development Master’s degree in either Chemical Engineering, Biochemical Engineering or a related field Exp: 1-2 years |
Regeneron’s Late-Stage Purification Development team within PMPD (Preclinical Manufacturing and Process Development) is seeking an energetic Process Development Engineer I. In this role, you will be responsible for the development, characterization, and transfer of various membrane-based downstream purification processes, including viral retentive filtration, ultrafiltration/diafiltration, and sterile filtration for recombinant proteins, using Quality by Design principles. | 01/28/2025 |
| 1767 | REGENXBIO Rockville, MD Manufacturing Associate Contractor Bachelor’s degree Exp: 0-2 years |
REGENXBIO is currently looking for a highly motivated individual to join our Manufacturing Operations team! As a contract-member of the highly engaged and collaborative group, you will have the unique opportunity to start-up an agile, multi-product, single-use facility. You will be accountable for supporting the establishment of new processes, procedures and ways of working, as well as performing manufacturing process related tasks and unit operations within the Upstream and Downstream areas. | 01/28/2025 |
| 1768 | Renaissance Lakewood, NJ Compounder II, 3rd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 01/28/2025 |
| 1769 | Renaissance Lakewood, NJ Compounder II, 2nd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 01/28/2025 |
| 1770 | Renaissance Lakewood, NJ Compounder II, 1st shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 01/28/2025 |
| 1771 | Repligen Corporation Bridgewater, NJ Laboratory Support Specialist Bachelor’s degree in a related field (e.g. Biology, Chemistry) Exp: 1 year |
The VPT Support Specialist is responsible for providing technical assistance and expertise to the CTI/Repligen sales force and customers related to the laboratory instrumentation its sells and supports. The laboratory technology developed and marketed by CTI/Repligen includes variable path length UV/Vis spectroscopy instrumentation. The systems are sold primarily into the pharmaceutical and biotech industry and are commonly used for quantifying concentrations of proteins and antibodies in drug discovery and development, manufacturing, and quality assurance. The VPT Support Specialist will provide support both at CTI/Repligen and on site at customer locations. The type of support will include system qualifications for Installation and Operation (IQOQ), product testing, system maintenance and customer training. Delivering training and support will involve travel to customer locations both domestic and international. Training will be provided by CTI/Repligen. | 01/28/2025 |
| 1772 | Repligen Corporation Raleigh, NC Laboratory Support Specialist Bachelor’s degree in a related field (e.g. Biology, Chemistry) Exp: 1 year |
The VPT Support Specialist is responsible for providing technical assistance and expertise to the CTI/Repligen sales force and customers related to the laboratory instrumentation its sells and supports. The laboratory technology developed and marketed by CTI/Repligen includes variable path length UV/Vis spectroscopy instrumentation. The systems are sold primarily into the pharmaceutical and biotech industry and are commonly used for quantifying concentrations of proteins and antibodies in drug discovery and development, manufacturing, and quality assurance. The VPT Support Specialist will provide support both at CTI/Repligen and on site at customer locations. The type of support will include system qualifications for Installation and Operation (IQOQ), product testing, system maintenance and customer training. Delivering training and support will involve travel to customer locations both domestic and international. Training will be provided by CTI/Repligen. | 01/28/2025 |
| 1773 | Repligen Corporation Lebanon, NH Associate Scientist - Quality Control Bachelor's Degree with experience in a scientific environment Exp: 1-3 years |
Repligen is seeking an Associate Scientist to join our expanding Quality team. | 01/28/2025 |
| 1774 | Repligen Corporation Marlborough, MA QA Associate I, Hollowfiber BA/BS degree (in a Biological Science, Engineering, or Physical Science) Exp: 0-2 years |
We are currently seeking a QA Associate I to join our Quality team in Marlborough, supporting Hollow Fiber and Single Use ATF Manufacturing. The QA Associate I will actively participate in the Repligen ISO 9001 Quality Management System, reviewing production records and releasing product, as well as supporting other QA team members and areas of work, as needed. The successful candidate will have a positive attitude and be able to communicate effectively. This candidate will be responsible for assisting the QA department to revise/create, file, organize, and review production documents. The candidate will work closely with the manufacturing teams to ensure accuracy of production documentation throughout the production process. This position involves completing the QA review of production records, including but not limited to; verification of raw materials used, verification of calculations, good documentation practices, and processing steps have been completed according to the internal processes. | 01/28/2025 |
| 1775 | Repligen Corporation Anaheim, CA Automation Engineer B.S. Degree in Mechanical, Electrical, Computer Science, Industrial Engineering Exp: 1-3 years |
The automation engineer will report directly to the R&D Automation lead. | 01/28/2025 |
| 1776 | Replimune Framingham, MA Manufacturing Associate I/II Bachelor’s degree Exp: 1-3 years |
The Manufacturing Associate I/II is responsible for executing the cGMP manufacturing operations to support the production of Replimune products at the Framingham, MA, facility. This individual will collaborate with multiple departments to support the manufacturing production facility. They will assist with the generation/revision of Standard Operating Procedures and associated documentation to ensure manufacturing readiness. | 01/28/2025 |
| 1777 | Replimune Framingham, MA Sr. Associate, Technical Operations Master’s degree in chemical or biomedical engineering or equivalent Exp: 0-3 years |
The Technical Operations Engineer I/II will be responsible for providing drug substance and/or drug product technical support for oncolytic virus manufacturing. This includes life cycle management of commercial processes, including ownership and support of change controls, CAPAs and deviations. | 01/28/2025 |
| 1778 | Replimune Framingham, MA Manufacturing Technician Bachelor’s degree Exp: 0 years |
Reporting to the Manufacturing Manager, the Manufacturing Technician will be part of a cohesive team responsible for producing RPX at Replimune’s Framingham Manufacturing Facility. The Manufacturing Technician will support production processes by operating, set up, changeover, and cleaning of various automated and manual equipment in strict accordance with SOP’s, Good Manufacturing Practices, and Safety policies/procedures. The manufacturing Technician will support the Manufacturing Team in day-to-day operations. | 01/28/2025 |
| 1779 | Replimune Framingham, MA Manufacturing Specialist I Master’s degree Exp: 0-2 years |
The Manufacturing Specialist I and II will be part of a cohesive team responsible for producing RPX at Replimune’s Framingham Manufacturing Facility. The Manufacturing Specialist uses expert knowledge of cGMP regulations and biopharmaceutical production processes to provide day to day operational support through the implementation of process improvements, leading manufacturing activities, supporting the scheduling of daily manufacturing activities and deviation/CAPA/change control writing with a focus on but not limited to Commercial/Clinical Manufacturing. | 01/28/2025 |
| 1780 | Resolution Medical Fridley, MN Product Development Engineer II - Test Method Bachelor’s degree in related field Exp: 1-3 years |
Activities include product design and development, defining technical solutions to abstract problems, defining methods and processes, design modeling, tooling design/fabrication, equipment design/fabrication, personnel management, design verification and validation, and documentation. Participate in the day-to-day execution of reliability tasks by teams and team members through monitoring progress, providing technical direction, and problem-solving solutions. Subject matter expert on test method development and design verification. Primarily by driving the testing of device, assist in design and develop innovative products & manage the product design from concept to full production. This position will participate in the execution of development projects as part of a multi-functional project team with an emphasis on the V&V activities. | 01/28/2025 |
| 1781 | Restor3d Wilmington, MA Manufacturing Engineer Bachelor’s Degree in Engineering Exp: 0-2 years |
The Manufacturing Engineer I will be responsible for the selection, development, qualification, and scale-up of production processes and equipment across different manufacturing departments. Process objectives are the high quality, high volume production of patient-tailored implants and associated instruments. | 01/28/2025 |
| 1782 | Retro Redwood City, CA Research Associate M.S in Biology or related field Exp: 1 year |
We are hiring a new member of the Microglia Therapeutics team who will be involved in making iPSC-derived microglia, characterizing them, and developing them into cellular therapy product. In this role, you will enable the microglia team to move faster and iterate more quickly by increasing the capacity for hands-on work in the lab. | 01/28/2025 |
| 1783 | Revolution Medicines Redwood City, CA Clinical Trial Assistant II, Clinical Operations Bachelor’s degree in biological sciences or related health related field Exp: 1-3 years |
As a Clinical Trial Assistant II in Clinical Operations, initially reporting to the Director Clinical Operations, you will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support RevMed clinical trials. | 01/28/2025 |
| 1784 | Revolution Medicines Redwood City, CA Clinical Trial Assistant II - Clinical Operations Process and Systems Bachelor’s degree in biological sciences or health-related field Exp: 0-1 years (CTA I)/1-3 years (CTA II) |
This is a unique opportunity for an entry-level Clinical Operations Professional. As the Clinical Trial Assistant II, Clinical Operations Process and Systems, you will be responsible for acting as an integral member of the Clinical Operations team and will be tasked to support the management of Clinical Operations processes and systems, in support of execution of RevMed’s clinical trials. | 01/28/2025 |
| 1785 | Rion Rochester, MN Research Associate, Analytical Development Bachelor’s or Master’s degree with focus in Biological Sciences Exp: 1+ years |
The Analytical Development Research Associate will contribute to analytical method development, implementation, and validation of methods focused on Rion’s exosome technology. This role will work closely with Rion Quality Control to execute method transfers and support continuous improvement. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, ELISA, RT-qPCR, HPLC and colorimetric/fluorometric-based assays. The Analytical Development Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Analytical Development Research Associate will work closely with the Analytical Development Scientists and support the efforts of Quality Control Development. As such, the successful candidate will work in an upbeat, highly collaborative, and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 01/28/2025 |
| 1786 | Roche Little Rock, AR Field Engineering Specialist - Fort Smith, AR Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1787 | Roche Seattle, WA Field Engineering Specialist - Seattle, WA Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1788 | Roche Evansville, IN Field Engineering Specialist - Evansville, IN Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1789 | Roche Milwaukee, WI Field Engineering Specialist - Milwaukee, WI Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1790 | Roche Scranton/Wilkes Barre, PA Field Engineering Specialist - Scranton & Wilkes Barre, PA Bachelor's degree in a relevant field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist, you will travel and showcase your expertise in technical repair and installation for Roche assigned product lines. You will offer valuable service to laboratory customers in your assigned territory. The role involves routine technical support, on-site service, repair, and installation of Roche products. You will serve as a customer contact for technical and service-related issues and perform preventative maintenance. The position requires diagnosing and resolving mechanical, hardware, software, and system failures. You will document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1791 | Roche Cape Girardeau, MO Field Engineering Specialist - Cape Girardeau, MO Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1792 | Roche Birmingham, AL Field Engineering Specialist - Birmingham, AL Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1793 | Sanguine San Diego, CA Lab Technician I Bachelor’s degree Exp: 1 year |
The Entry Level Lab Technician I will be responsible for the processing and testing of various blood samples. Sample processing will include, but is not limited to: PBMC, T, B, & NK cell isolations. Other assigned duties may include cell counting, aliquot preparation, accessioning, reagent creation, proper storage, flow cytometry lab services. Initial samples will be from both Leukopaks and blood samples or its derivatives. This role will also require experience with LIMS systems and commercial laboratory operations, including the internal communication of project details with Sanguine personnel as well as the ability to work as a team. | 01/28/2025 |
| 1794 | Sanofi Swiftwater, PA Senior Production Technician - Vaccines Bachelors Exp: 1+ years |
The Senior Production Technician will: Ensure operational area is running as intended to meet all operational goals. Ensures the completion of Environmental Monitoring sampling and corresponding documentation, data entry, and delivery as required during all aseptic processing. Real time review of this documentation. We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world. | 01/28/2025 |
| 1795 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelor’s degree Exp: 0 years |
Sanofi is seeking a motivated professional candidate to operate within Biologics production and perform manufacturing activities. This is an exciting opportunity for a candidate to develop technical skills and learn about the biopharmaceutical industry. The production technician will operate in a cGMP manufacturing area performing equipment set up and operations tasks to meet all standards for safety, quality, and efficiency. The candidate will perform production in accordance with volume fluctuation, business need, and effective procedures. | 01/28/2025 |
| 1796 | Sanofi Cambridge, MA Associate Scientist - Medicinal Chemistry, Integrated Drug Discovery Bachelor’s Degree Exp: 1 year |
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. As a Associate Scientist - Medicinal Chemistry, Integrated Drug Discovery, your skills could be critical in helping our teams accelerate progress. Synthetic organic chemist with deep knowledge of organic chemistry principles and modern synthesis methods to design and execute efficient synthetic routes for target compounds and the progression of drug discovery projects. | 01/28/2025 |
| 1797 | Sciex Atlanta, GA Field Service Technician - Atlanta, GA Bachelor's degree (B.S./B.A.) in Life Sciences, Chemistry, or Engineering Exp: No exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Sciex products at both internal and external customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position reports to the District Service Manager and is part of the Field Technical Service organization working remotely to cover Atlanta GA. | 01/28/2025 |
| 1798 | Sedia Biosciences Beaverton, OR QC Assistant Scientist B.Sc. in applicable biological science or chemistry. Exp: Entry Level |
Sedia Biosciences is hiring a QC Assistant Scientist at our Beaverton, Oregon location. At Sedia, we create diagnostic and disease-monitoring products that provide cost effective solutions for rapid, near patient testing. We are currently seeking responsible individuals motivated to help research and develop our future diagnostic products. This position performs simple laboratory activities related to the inspection and testing or raw materials, components, and finished products in a medical diagnostic development and manufacturing environment following specific instructions from more senior Quality Control personnel or by following technical instructions | 01/28/2025 |
| 1799 | LGC Clinical Diagnostics Cumberland Foreside, ME Quality Control Technologist I Bachelor’s degree in Medical Technology (preferred) or related science degree (i.e. biology, chemistry, biochemistry) Exp: 1-3 years |
Follows standardized procedures and prepares samples for testing. Analyzes test results for accuracy, acceptability, and critical limits. Relies on limited independent judgment to plan and accomplish goals. Performs a variety of tasks. A limited degree of creativity and latitude is required. | 01/28/2025 |
| 1800 | LGC Clinical Diagnostics Milford, MA Manufacturing Associate I/II Bachelor’s degree, with a concentration in Biology, Chemistry, or related science Exp: 1-3 years |
The Manufacturing Associate I / II provides direct labor for the manufacturing of high-quality diagnostic products using manual and semi-automated equipment and prepares/completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 01/28/2025 |
| 1801 | LGC Clinical Diagnostics Milford, MA Manufacturing Associate II Bachelor’s degree, with a concentration in Biology, Chemistry, or related science Exp: 1-3 years |
The Manufacturing Associate II provides direct labor for the manufacturing of high-quality diagnostic products using manual and semi-automated equipment and prepares/completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 01/28/2025 |
| 1802 | SGS Dayton, NJ Lab Analyst I - PFAS Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 1-2 years |
Our Dayton, NJ laboratory is looking for a laboratory analyst to join their team! The Lab Analyst will prepare and analyze samples with accuracy and precision in accordance to SGS' analytical SOPs. Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. Understand and apply basic analytical chemistry principles. Always follow safe laboratory practices and maintain a safe working environment. | 01/28/2025 |
| 1803 | SGS Seabrook, TX Chemist Bachelor’s Degree in Chemistry or a related science preferred Exp: 1 year |
Responsible for analysis and reporting of various products such as crude oil, fuel oils, middle distillates, petroleum and petrochemicals, LPG & LNG gases, etc. | 01/28/2025 |
| 1804 | SGS Lincolnshire, IL Microbiologist I BS degree in Microbiology or related sciences Exp: 0-2 years |
The Microbiologist I works independently on assigned Microbiological projects and conducts analyses of raw materials, finished products, and waters. As a professional scientist, the Microbiologist is expected to work under the guidance of supervisors and managers, develop skills and understanding of laboratory procedures, exhibit technical expertise, be able to document data and report findings; and stay current with Microbiological literature and standards for analyses. You will also conduct analyses of samples in accordance with USP, EP, ASTM, AOAC, FDA, EPA procedures, procedures supplied by the client, and other non-routine procedures as encountered. | 01/28/2025 |
| 1805 | SGS Anchorage, AK Laboratory Analyst Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 1-2 years |
Our Anchorage, AK laboratory is looking for a Laboratory Analyst to join our team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory Analyst always follows safe laboratory practices and maintains a safe working environment. | 01/28/2025 |
| 1806 | Pfizer Andover, MA Process Technician-Purification Bachelor's degree Exp: 1 year |
You will support the execution of production according to Standard Operating Procedures and production schedule. Working with interdisciplinary teams, you will implement process improvements and participate in process troubleshooting. As part of technical operations, you will be developing and applying your knowledge of procedures, techniques, tools, materials and equipment. Your receptiveness to new ideas will enhance the team’s ability to achieve goals and targets. You will follow standard procedures to complete tasks and identify process issues or problems that involve direct application of your skills/knowledge. It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe. | 01/21/2025 |
| 1807 | Pfizer Sanford, NC Manufacturing Quality Support Senior Associate Master's degree in microbiology, chemistry, biological sciences, bioengineering Exp: 1+ years |
The Manufacturing Quality Support Senior Associate provides Quality Assurance (QA) support to clinical, commercial, and contract manufacturing operations. The role ensures adherence to regulatory expectations, safety, and GxP (i.e., Current Good Manufacturing and Documentation Practices).The role is based at the Pfizer Sanford, NC Pfizer Global Supply (PGS) site. | 01/21/2025 |
| 1808 | Pfizer Groton, CT Senior Associate Scientist MS in Chemical, Mechanical, Electrical or Pharmaceutical Engineering, Physics or Engineering Physics, Computer Science, Pharmaceutics, or other relate Exp: 0-3 years |
Pfizer’s Drug Product Design group is seeking team members with a desire to bring new, cutting-edge medicines to patients around the world. Our team members use science and technology to design, characterize and develop drug product formulations from candidate selection to commercial launch. You will be able to leverage your existing scientific knowledge, as well as develop scientific knowledge in new areas, to evaluate the chemical & physical stability, bio-performance and manufacturability of the drug product across a diverse range of therapeutic areas. You will complete experimentation using conventional and continuous drug product manufacturing equipment and participate in multi-disciplinary teams during the formulation development, process scale up, and technology transfer of conventional and continuous processing technologies to our clinical R&D manufacturing sites, as well as our commercial manufacturing sites within the Pfizer Global Supply organization. You will also apply your engineering, additive manufacturing/3D printing, and rapid prototyping skills to improve machine design, develop and apply advanced computational models and data analysis, and advanced sensing capabilities to the drug product manufacturing. This laboratory-based position offers the opportunity for cross-training and growth in multiple technical areas to encourage a flexible working environment. Enjoy the entrepreneurial mindset and infrastructure to develop new technologies and processes for drug delivery and dosage form manufacture while having access to the resources of a larger company. Excellent laboratory and communication skills, attention to detail, the ability to solve technical problems, and the diligence to maintain thorough electronic laboratory notebook records of work performed are required. Finally, this position will challenge you to pursue scientific excellence and creativity, in collaboration with industry-leading experts across multiple scientific disciplines. | 01/21/2025 |
| 1809 | Pfizer Pearl River, NY Associate Scientist - Bioassay Development BS or BA degree in biology or related discipline Exp: 0-2 years |
This is a laboratory-based position within Pfizer’s Vaccine Research and Development (VRD) organization – Analytical Development group. The candidate assists with development of robust analytical assays in support of early vaccine development for a range of moieties such as mRNAs, proteins, and glycoconjugates. Representative assays include, but are not limited to, cell-based assays monitored by Flow Cytometry, Enzyme-Linked Immunosorbent Assays (ELISAs), and Bioplex/Luminex. The candidate also provides analytical support for bioprocess and formulation development by performing routine/non-routine sample testing. Your strong foundation in general scientific practice, principles, and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. It is your focus and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe. | 01/21/2025 |
| 1810 | Pfizer Pearl River, NY Associate Scientist BS or BA degree in biology or related discipline Exp: 0-2 years |
This is a laboratory-based position within the Vaccine Research and Development – Analytical Development group. The candidate contributes to the development of robust analytical assays to support early vaccine development for a range of moieties including proteins, mRNA, and glycoconjugates. Assays include but are not limited to cell-based assays such as flow cytometry, enzyme-linked immunosorbent assays (ELISAs), and immunofluorescence. In addition, the candidate provides analytical support for bioprocess and formulation development through characterization testing of preclinical products. Your strong foundation in general scientific practice, principles, and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. It is your focus and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe. | 01/21/2025 |
| 1811 | Pfizer McPherson, KS Senior Process Engineer Masters Exp: 0+ years |
The role is to provide senior level engineering business partnership to the packaging and manufacturing operations leaders. The role will partner with operations, engineering, maintenance and reliability teams to drive overall Equipment and Process improvement and key strategic projects. The role must demonstrate ability to accomplish large and complex projects independently, provide engineering expertise and lead structured troubleshooting efforts of major equipment and process-related issues. Analyzes process requirements and evaluates equipment and systems to ensure deliverables meet or exceed process specifications and packaging/manufacturing requirements. Evaluates and recommends new process technologies that optimize performance, are cost effective, and will improve product quality and manufacturing processes. | 01/21/2025 |
| 1812 | Pfizer Rochester, MI Sr. Automation Compliance Engineer Master’s degree Exp: 1+ year |
The Sr Automation Compliance Engineer will have overall responsibility for managing regulatory aspects of the process automation and control systems used in the manufacture of sterile injectable. This position will provide engineering and technical support related to the operation, maintenance, installation, startup/commissioning, testing, and qualification of systems within a sterile injectable manufacturing facility. | 01/21/2025 |
| 1813 | Caris Life Sciences Phoenix, AZ Quality Assurance Technologist, Solid Tumor Bachelor's degree in a science field. Exp: 1 year |
A Quality Assurance Technologist is responsible for a multitude of different tasks within the clinical molecular laboratory including the quality control testing of all molecular reagents prior to use on clinical samples, assisting the product development team with the validation of new assays and training current employees on new assays as well as new employees on established assays. This position is required to be well versed in various molecular techniques that include, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, RFLP, DNA methylation analysis, Next Generation sequencing and automated liquid handlers. Quality Assurance Technologists are expected to contribute technically and intellectually to enhance efficiency within the lab while ensuring that the quality of reagents and training program is maintained to the highest standard. This position works under the direction of the Director and follows standard laboratory procedures and policies. | 01/21/2025 |
| 1814 | Caris Life Sciences Phoenix, AZ Pathologist Associate Bachelor’s degree in a field of science Exp: 0-1 year |
The Pathologist Associate is responsible for supporting and assisting the Pathology and Pathology Operations departments in their daily operations. This position will perform tasks needed to be completed in the day-to-day operation. This position also includes performing the tasks of Macrodissection and Microdissection. | 01/21/2025 |
| 1815 | Quest Diagnostics Denver, CO Lab Associate II Bachelor’s Degree Exp: 1 year |
Prepares and organizes samples for testing, for example, sample racking, aliquoting and tube preparation. Responsible for labeling, handling, processing or preparation, and transportation and storage of specimens. Identifies sample problems and assists in resolving appropriately. Demonstrates problem solving ability on service and production issues. Prepares testing equipment and assists with preventive maintenance. Notifies appropriate technical staff of equipment problems. Assists licensed personnel (CA only) or delegated supervisor (non-CA) in the pre-analytic and post-analytic testing activities, other than trainees, in a licensed clinical laboratory. Prepares pre-analytical reagents and controls using automated or fixed volume measuring devices. Submits documentation to appropriate staff for approval to use. Prepares and maintains complete and accurate records of reagents or media using established procedures, formulas, stock solutions and fixed volume measuring devices. Maintains inventory of consumable items including reagents and supplies. Orders, unpacks, logs, dates and stores reagents/supplies upon receipt and properly rotates stock for use. Performs inventory of laboratory items including restocking the benches and equipment inventory. Sorting and accessioning incoming specimens into appropriate LIS, then delivering to designated testing platform/department. Performs data entry or transcribes data from previously recorded results to computer for data reduction and prepares for licensed personnel's review. Tallies workload data and prepares reports as requested. Assists in the performance of quality control procedures. Prepares protocols/logs or other appropriate documents. Identifies specimen problems and demonstrates ability to appropriately resolve or elevate to licensed personnel (CA only) or delegated supervisor (non-CA). Assists a licensed person (e.g.: CLS) with performance of validation verifications and other Research and Development (R&D) activities, as applicable. Trains other Lab Associates. Supports Training Programs, where applicable. Takes initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. Is a resource for process improvement. Demonstrates leadership through accountability and collaboration in daily activities. Answers phones, transfers, or takes accurate messages. Maintains the confidentiality of client information. Helps to ensure the laboratory areas are neat, clean, and o | 01/21/2025 |
| 1816 | Quest Diagnostics Cleveland, OH Lab Associate II Bachelor’s Degree Exp: 1 year |
Prepares and organizes samples for testing, for example, sample racking, aliquoting and tube preparation. Responsible for labeling, handling, processing or preparation, and transportation and storage of specimens. Identifies sample problems and assists in resolving appropriately. Demonstrates problem solving ability on service and production issues. Prepares testing equipment and assists with preventive maintenance. Notifies appropriate technical staff of equipment problems. Assists licensed personnel (CA only) or delegated supervisor (non-CA) in the pre-analytic and post-analytic testing activities, other than trainees, in a licensed clinical laboratory. Prepares pre-analytical reagents and controls using automated or fixed volume measuring devices. Submits documentation to appropriate staff for approval to use. Prepares and maintains complete and accurate records of reagents or media using established procedures, formulas, stock solutions and fixed volume measuring devices. Maintains inventory of consumable items including reagents and supplies. Orders, unpacks, logs, dates and stores reagents/supplies upon receipt and properly rotates stock for use. Performs inventory of laboratory items including restocking the benches and equipment inventory. Sorting and accessioning incoming specimens into appropriate LIS, then delivering to designated testing platform/department. Performs data entry or transcribes data from previously recorded results to computer for data reduction and prepares for licensed personnel's review. Tallies workload data and prepares reports as requested. Assists in the performance of quality control procedures. Prepares protocols/logs or other appropriate documents. Identifies specimen problems and demonstrates ability to appropriately resolve or elevate to licensed personnel (CA only) or delegated supervisor (non-CA). Assists a licensed person (e.g.: CLS) with performance of validation verifications and other Research and Development (R&D) activities, as applicable. Trains other Lab Associates. Supports Training Programs, where applicable. Takes initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. Is a resource for process improvement. Demonstrates leadership through accountability and collaboration in daily activities. Answers phones, transfers, or takes accurate messages. Maintains the confidentiality of client information. Helps to ensure the laboratory areas are neat, clean, and o | 01/21/2025 |
| 1817 | Quest Diagnostics San Juan Capistrano, CA Lab Associate II - Immunology Bachelor’s Degree Exp: 1 year |
This non-licensed position is accountable for assisting with general support for the laboratory, following all applicable policies and procedures. | 01/21/2025 |
| 1818 | Quest Diagnostics San Juan Capistrano, CA Lab Associate II - Hematology Bachelor’s Degree Exp: 1 year |
This non-licensed position is accountable for assisting with general support for the laboratory, following all applicable policies and procedures. | 01/21/2025 |
| 1819 | Pion Billerica, MA Laboratory Scientist Bachelor’s or Master's degree in Chemistry or preferably Biochemistry required Exp: 1+ year |
The Laboratory Scientist is responsible for supporting and executing experimental work to complete analytical service projects and for supporting the development of chemical and biopharmaceutical testing equipment and innovative applications. | 01/21/2025 |
| 1820 | Pledge Therapeutics Canton, MA Research Associate, Immuno-Oncology MS Exp: 1-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our new state-of-the-art facility in Canton, MA. The successful candidate will engage in the Immuno Oncology research areas of the company and will work with a successful team of international senior scientists located in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 01/21/2025 |
| 1821 | Pledge Therapeutics Canton, MA Research Associate, Virology Bachelor’s or Master’s degree in biological sciences or a related field Exp: 0-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our state-of-the-art facility in Canton, MA. The successful candidate will engage in the company’s virology research areas and work with a successful team of scientists in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 01/21/2025 |
| 1822 | PolyPeptide San Diego, CA Production Chemist BS degree in Chemistry or Biochemistry or equivalent Exp: 1+ years |
Checks reactor system for proper operation in accordance with SOP and/or operation manual. Under general supervision and direction, measures and mixes ingredients according to the BPR (Batch Production Record). Dispensing of raw materials from Pharmastore for Synthesis. During processing, monitors chemical reactions (color and completeness of chemical reactions) and under general direction of supervision and/or senior Production Chemist personnel responds with appropriate actions to ensure proper processing. Using established procedures (safety and process) and under general supervision, performs intermediate chemical processing steps. Prepares solutions for purification and samples. Under general supervision, purifies crude peptide by using HPLC’s. Conducts lyophilization process according to established guidelines. Performs drying processes in accordance with established processes and procedures. Reports any problems or issues regarding equipment used in processing to supervision and/or senior Production Chemist personnel. Performs in-process checking of the fractions by using analytical HPLC and reports results to supervision and/or Sr. Production Chemist personnel. Is responsible for maintaining high safety, housekeeping and cleanliness standards. Performs any and all additional duties as required for this position. | 01/21/2025 |
| 1823 | Polysciences Warrington, PA Quality Control Analyst I Bachelor’s degree in chemistry, chemical engineering or a similar field Exp: 1+ years |
We’re hiring a Quality Control Analyst in our Quality Control group who will use analytical equipment, analytical methods, and perform data analysis. Will test using GC, HPLC, LC/MS, KF, FTIR, UV-Vis, Viscometers, and Atomic Absorption, NMR, etc. | 01/21/2025 |
| 1824 | ProKidney Winston-Salem, NC Manufacturing Cell Processing Specialist 1 BS in Biotechnology, Biology, Chemistry, or related field; a Science-related discipline Exp: 0-2 years |
The Manufacturing Specialist, Cell Processing at ProKidney is responsible for supporting cell processing operations, ensuring compliance with cGMP guidelines in the development and production of regenerative medicine therapies. This role involves setting up and operating production equipment, including control rate freezers, orbital shakers, and other equipment, while contributing to efficient processing, freezing, and storage of cell therapy products. | 01/21/2025 |
| 1825 | ProKidney Winston-Salem, NC Cell Processing Specialist (Contractor) BS in Biotechnology, Biology, Chemistry, or related field; a Science-related discipline Exp: 0-2 years |
The Manufacturing Specialist, Cell Processing at ProKidney is responsible for supporting cell processing operations, ensuring compliance with cGMP guidelines in the development and production of regenerative medicine therapies. This role involves setting up and operating production equipment, including control rate freezers, orbital shakers, and other equipment, while contributing to efficient processing, freezing, and storage of cell therapy products. | 01/21/2025 |
| 1826 | ProKidney Winston-Salem, NC Manufacturing Support Specialist 1 BS in Biotechnology, Biology, Chemistry, or related field Exp: 0-2 years |
The Manufacturing Support Specialist I is essential in supporting manufacturing operations and maintaining the sterility and cleanliness of GMP facilities. This role involves aseptic processing of in-house solutions, media and kit preparation, GMP cleaning, and supporting manufacturing cell processing teams. The specialist is responsible for ensuring compliance with current Good Manufacturing Practices (cGMP), performing routine aseptic processing, preparing cleaning solutions for cleanroom sanitization, and ensuring proper documentation for biopsy and product shipments. This role also contributes to maintaining controlled environments, executing cleaning procedures, managing inventories, and collaborating with teams to improve manufacturing processes and cleanliness protocols. | 01/21/2025 |
| 1827 | Promis Dx Irvine, CA Laboratory Technician BS in Biology, Chemistry, or other medical-related sciences Exp: Entry level |
The Laboratory Assistant or Technician will follow the guidelines set by CLIA and the CA Business and Professional Code of Regulations (BPC: 1212 and 1269) for unlicensed laboratory personnel. | 01/21/2025 |
| 1828 | PsychoGenics Paramus, NJ Research/Data Analysis Assoc. Bachelor's degree in the biological scienes or related field Exp: 1-3 years |
We are looking for a highly motivated Researcher who can use, edit, and maintain our custom data processing software for our EEG group. The candidate must also work in a lab setting and will handle and work with rodents. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The candidate must be capable of working both across teams and independently. The candidate will have support and training for the laboratory work from other EEG staff and will have support on the programming side from our Data Sciences team. The candidate will work with all senior staff in the EEG group and will work closely with the VP, Translational Neuroscience on developming the custom software to perform additional functions and analyses. | 01/21/2025 |
| 1829 | PTC Therapeutics Bridgewater, NJ Contract, Biology Master’s degree in a scientific discipline, preferably Biology, Biochemistry, or Neuroscience Exp: 0-1 years |
The Contract, Biology is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. The Contract, Biology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. | 01/21/2025 |
| 1830 | Purolite Resins (EcoLab) Philadelphia, PA R&D Technical Analyst Bachelor’s degree Exp: 1 year |
Ecolab is looking for a R&D Technical Analyst who will perform a variety of routine tasks to maintain product specifications including mechanical or chemical characteristics of an item or product, who will work under minimal supervision and receive instruction only as necessary. The successful candidate will work on assignments and performs tasks that are moderately complex, where discretion is required in resolving problems and making routine recommendations regarding creation or maintenance of product specifications. | 01/21/2025 |
| 1831 | QIAGEN Germantown, MD Metrology Technician BS/BA Exp: 1-3 years |
The Metrology Technician performs equipment calibration assignments using standard methods and processes. Required duties include: Set-up, calibration, testing, repair, inspection and maintenance of equipment and tools. Making adjustments, modifications or replacements as needed. Maintain and document calibration of all measurement equipment (in the Electronic Calibration Maintenance Management System). Creating, maintaining, and updating department SOPs and other documentation as required. Coordinate the execution of the calibration program to include event scheduling, performance, and oversight of service suppliers. Provide notification of calibration tasks with due dates. Coordinate calibration scheduling with equipment owners when needed. Oversee work by outside calibration contractors to ensure compliance with applicable procedures. Troubleshoots and solves calibration and maintenance problems of moderate scope and complexity requiring broad technical interpretation of defined procedures and practices. Responsible for ensuring on-going compliance to applicable quality and EHS regulations and standards (e.g., cGMP, FDA, ISO, IVDD, OSHA, etc.). | 01/21/2025 |
| 1832 | Quality Agents Rockville, MA Quality Assurance Specialist BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Quality Assurance Specialists are leading service providers to our clients providing GMP support. The individual will coordinate validation activities with the client and meet timelines. | 01/21/2025 |
| 1833 | Quality Agents Rockville, MA Validation Engineer I BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by the client. | 01/21/2025 |
| 1834 | QuidelOrtho Rochester, NY V&V Engineer I (R&D) B.S. Degree in Computer Science, Chemistry, Biochemistry, Biology, Engineering, or a related discipline Exp: 1-2 years |
As QuidelOrtho continues to grow, we are seeking a Verification and Validation Engineer I to help with formal verification and validation of complex medical devices under the regulations of the FDA. The individual will be part of an engineering team that is responsible for requirements based test design and execution of test procedures both in a virtual and lab environment. The team is highly collaborative and will require regular interactions in formal reviews, test planning activities, and working with software development to reproduce and verify system defects. | 01/21/2025 |
| 1835 | QuidelOrtho Carlsbad, CA Quality Engineer B.S. Degree in Chemistry, Biochemistry, Biology, Engineering, or a related discipline Exp: 1+ years |
As we continue to grow as QuidelOrtho, we are seeking a Quality Engineer. This position is responsible for owning and coordinating all Quality Engineering functions and activities for the defined processes. This individual is also responsible for supporting the Production, Quality Control, Engineering and Quality Assurance departments and the associated activities, which include receiving inspection, in-process inspection, and finished goods inspection in achieving and exceeding company goals and objectives. In addition, this individual is responsible for supporting the administration, implementation, and continuous improvement of the quality systems associated with non-conforming materials, inspection control plans, and corrective/preventive action. This individual also supports corporate strategic goals and objectives through internal audits, support of manufacturing operations, quality support for manufacturing processes for new product development/ product improvement projects, and support of manufacturing process improvement projects. | 01/21/2025 |
| 1836 | QuidelOrtho Athens, OH Associate Biochemist Bachelor’s Degree in a biology, biochemistry, chemistry or other related science field Exp: 1 year |
The Associate Biochemist is responsible for the production and quality testing of various raw material, intermediate components and finished good catalog items, in accordance with Quidel’s Quality System Regulations. | 01/21/2025 |
| 1837 | QuidelOrtho Raritan, NJ Facilities Engineer BS in Engineering Exp: 1-2 years |
As the company continues to grow, we are seeking a Facilities Engineer to provide support of the facility equipment and supporting systems to efficiently maintain and reliably operate the site. The position will provide support of maintenance staffing services, assessment and control of performance metrics, and attainment of cost objectives in daily maintenance and operation of all facility assets. Supporting systems include maintenance work management, building control, quality, procurement, training, and all associated supporting procedures. Position is to continuously assess general condition and readiness of critical assets required to deliver business priorities without interruption. Position has overall responsibility for all infrastructure and staffing capability to ensure reliable and efficient facility operations. Deliver high quality, safe, compliant, cost effective facilities infrastructure. | 01/21/2025 |
| 1838 | Quintara Discovery Hayward, CA Senior Research Associate Master’s degree in Biology or related field. Exp: 1 year |
Responsible for exercising independent judgment in conducting research on in vitro ADME screening (ADME: Absorption, Distribution, Metabolism, and Elimination): plan experimental approaches; design and carry out bioanalytical tests of various compounds for the potential development of human therapeutics; analyze and interpret experimental data and prepare reports of findings. Design and perform procedures in ADME assay projects by operating lab equipment, including integrated hardware, software, optical and fluidic subsystems. Conduct sample bioanalysis and develop bioanalytical methods for the quantitative analysis by using mass spectrometry. Document information on procedures, modifications, and methods; maintain records of experiments and results in the accessible format. | 01/21/2025 |
| 1839 | Quotient Sciences Boothwyn, PA Validation Engineer BS Degree in Engineering Exp: 1-3 years |
This role will Provide engineering support for maintenance and validation activities. Maintain engineering documentation and support the completion and maintenance of both equipment impact and instrument assessments. Whilst complying & adhering to Good Manufacturing Practice (GMP) standards. | 01/21/2025 |
| 1840 | Quotient Sciences Garnet Valley, PA QC Scientist II Master’s degree in Chemistry or other related field of study Exp: 1+ years |
We have a full-time position available for an QC Scientist II at Quotient Sciences Philadelphia site in Garnet Valley. The QC Scientist II is responsible for analytical release and stability testing under the supervision of the Group Leader within the Clinical Quality Control Team. You will join a supportive team of experienced QC Analysts and perform the following duties. | 01/21/2025 |
| 1841 | Quotient Sciences Garnet Valley, PA Manufacturing Scientist B.S. Degree in Chemical Engineering, Pharmacy/Pharmaceutical Sciences or other related field Exp: Entry level |
Conduct lab work as planned by the supervisor that involves development of pharmaceutical formulations such as tablets, capsules, and liquids. Conduct pharmaceutical manufacturing of oral dosage forms using small to large-scale equipment for development and process scale-up and for clinical supplies. Review and write master batch records with input from the supervisor. Prepare executed batch record folders. Comply with cGMPs, SOPs, and Company policies. Operate manufacturing equipment with the Operator for development clinical manufacturing. Maintain a planned training schedule and record. Completion of clinical batch manufacturing as per timeline. Ability to perform physical work while using a respirator. Read and interpret documents such as batch records, SOPs, policies, and safety rules; read and write business correspondence. Define problems, collect data, establish facts, and draw valid conclusions. Interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Basic knowledge of physicochemical concepts and theories. Familiarity with the production process. Familiar with a variety of in-process equipment, such as disintegration, friability, particle size, etc. | 01/21/2025 |
| 1842 | Raybow Brevard, NC Synthetic Organic Chemist B.S. or M.S in Organic Chemistry Exp: 0-4 years |
Preferred candidates have work experience in multi-step synthesis of small molecules and should be able to design and develop practical synthetic routes to target compounds. A strong organic chemistry background with the ability to plan and execute complex syntheses is required. Successful candidates must have good verbal and written skills for communicating with management and clients. Excellent opportunity at all levels for growth and advancement. | 01/21/2025 |
| 1843 | Raybow Brevard, NC Analytical Chemist - Pharmaceutical B.S. or M.S in Organic Chemistry Exp: 0-4 years |
Preferred candidates have work experience in multi-step synthesis of small molecules and should be able to design and develop practical synthetic routes to target compounds. A strong organic chemistry background with the ability to plan and execute complex syntheses is required. Successful candidates must have good verbal and written skills for communicating with management and clients. Excellent opportunity at all levels for growth and advancement. | 01/21/2025 |
| 1844 | RayzeBio (Bristol Myers Squibb) San Diego, CA Associate Scientist, Chemistry BS or MS in Chemistry or related field Exp: 1-5 years |
RayzeBio is looking for an Associate Scientist to support in the development of novel therapeutics in preclinical stages. Candidates will work as part of a team of scientists to synthesize and design both small molecules and peptide analogs to optimize potency, pharmacokinetics, and in vivo efficacy of potential drug candidates. This position offers a challenging and rewarding work environment within a thriving company. | 01/21/2025 |
| 1845 | Reckitt Wanamingo, MN Compliance Assurance Lead/Associate Bachelor’s Degree in technical discipline (science/ engineering/ food processing, etc) Exp: 0-2+ years |
Manages and monitors site quality performance reporting requirements including root cause analysis, corrective action, and implementation to ensure compliance to QMS. Perform or review manufacturing non-conformance reports, CAPA, failure investigations, and audit findings to report manufacturing-related issues that may impact quality and recommend courses of corrective action. Prepare and analyze metrics for EM, CAPA, and suppliers’ performance to drive continuous improvement. Interface with suppliers to ensure the product meets specifications. Ensure compliance with all procedures for batch release. Develop knowledge of QC testing programs and capabilities. Assist in securing information for investigation, root cause, preventative action, and closure of non-conformities. Assist in the design and execution of validation protocols when required. Assist in the development and implementation of quality and productivity improvement projects. Perform HACCP GMP, Reckitt Nutrition Standards verification, and other quality and compliance audits as required. Ensure updates are made to the HACCP and Food Safety Plans based on the impact of changes in the plant from a Hazard Assessment and Risk-Based approach. Drive continuous improvement activities on the production line with training, SOP updates, etc. Other duties may be assigned. | 01/21/2025 |
| 1846 | Ofni Systems Raleigh, NC Computer Systems Validation Engineer BS or equivalent degree in math, science or engineering Exp: 1 year |
We are hiring a Validation Engineer to be on the cutting edge of automated validation techniques. You will be responsible for implementing our validation solutions while working with industry-leading companies. Ideal candidates are experts on the requirements of 21 CFR 11, have excellent critical thinking and interpersonal skills, and are motivated to meet client needs for compliance. If you are an A-level engineer who enjoys the challenge of solving real-world compliance problems then we would like to talk with you. | 01/16/2025 |
| 1847 | Olympus Brooklyn Park, MN Manufacturing Engineer II Master's degree in Engineering or Physics, or a related field Exp: 0+ years |
The position holder is responsible for the execution and documentation of process development deliverables and activities for Single Use Endoscopes (SUE) product development and launch to production. The position holder implements the optimal manufacturing processes according to product delivery, operations, and business requirements to launch products effectively, on time, with high reliability and the right cost. The position holder responsible for proactive engineering responses in alignment with Regulatory compliance requirements. | 01/16/2025 |
| 1848 | Olympus San Jose, CA Repair Engineer I Bachelor's Degree in Engineering Exp: 1 year |
Provide engineering support for introduction of new products and alternate repair activities. Function as Project Coordinator on more complicated projects as defined by the Manager by providing technical information to other project participants recommending cost effective procedures tracking and maintaining implementation dates and documenting completed projects. Provide support to Associate Engineer on his/her assigned projects. | 01/16/2025 |
| 1849 | Olympus Brooklyn Park, MN Manufacturing Engineer II Bachelor’s degree (B.S.) in science/engineering discipline or equivalent industry Exp: 0-2 years |
The Manufacturing Engineer-I will assist in supporting the day to day operation of the value stream or perform process development activities. They will strive to optimize processes for manufacture and product flow including down time mitigation, root cause investigations and cost savings initiatives. | 01/16/2025 |
| 1850 | Olympus Memphis, TN Repair Engineer I Bachelor's degree in engineering Exp: 1 year |
Provide engineering support for introduction of new products and alternate repair activities. Function as Project Coordinator on more complicated projects as defined by the Manager by providing technical information to other project participants recommending cost effective procedures tracking and maintaining implementation dates and documenting completed projects. Provide support to Associate Engineer on their assigned projects. | 01/16/2025 |
| 1851 | Olympus Brooklyn Park, MN R&D Engineer II Master’s degree in engineering (Biomedical or equivalent preferred) Exp: 0 years |
The Engineer II on the Sustaining Engineering team is responsible for supporting all aspects of Sustaining Engineering efforts, including supporting project definition activities, leading/supporting verification and validation efforts, and overseeing implementation. In particular, it will be the responsibility of the Engineer II to advance technical efforts, while proactively identifying potential issues, to achieve a timely launch of high quality / reliable product. He or she must have a working knowledge medical device design control requirement, be able to technically contribute to the project team, and work collaboratively across the organization to ensure an effective implementation of the improvement, solution, or line extension. As the Engineer II will contribute to Design History Files, maintaining detailed documentation throughout all phases of the project is essential. | 01/16/2025 |
| 1852 | OncoC4 Rockville, MD In-house CRA Bachelor’s degree in Sciences with strong emphasis in science and/or biology Exp: 1 year |
In house Clinical Research Associate (In-house CRA) will act as the clinical operations person to participate in IRB and TMF document submissions related to site selection, activation, maintenance, and closeout activities, in site monitoring and compliance management, and data integrity monitoring functions within OncoC4, supporting ongoing and future OncoC4 clinical trials of novel immune therapies for cancers. | 01/16/2025 |
| 1853 | OncoPep Cambridge, MA Research Associate (In Vitro) BS Exp: 1 year |
We are looking to expand our Research team by recruiting a skilled Research Associate in cellular/molecular biology to join our growing team. The candidate will primarily work with molecular and cell biology techniques including culture of primary cells and cell lines, flow cytometry, ELISA, and western blot. He/She will play an important role in the discovery and development of novel biotherapeutics for immuno-oncology. He/she will be responsible for generating the tools necessary for evaluation and screening of lead candidate therapeutics. He/she will be expected to participate in experimental design, conduct experiments, optimize throughput, maintain detailed records, and generate standard operating procedures. | 01/16/2025 |
| 1854 | Orchid Santa Ana, CA Quality Engineer Bachelor of Science (B.S) Exp: No exp |
The Quality Engineer I supports the ongoing quality of Orchid's legacy products & processes and works cross-functionally to sustain the business. | 01/16/2025 |
| 1855 | OrganaBio Miami, FL Cell Processing Associate Bachelor or Associate Degree in Biology, Cell and Molecular Biology, Biotechnology, Biomedical Engineering, or related field. Exp: 1-2 years |
This is a temporary role that has the possibility to convert to full time employment at the end of 90 days. A Cell Processing Associate assists in the performance of primary peripheral blood mononuclear cells (PBMCs) isolation from patient samples, as part of screening efforts for various customers. This position will help contribute to PBMC isolation process improvement, to drive efficiency in the documentation and production process. This role will support Process Development (PD) team efforts, and interact cross-functionally with teams that include, but are not limited to Business Development and Quality Assurance, to ensure company milestones are met. This position will ensure that products are processed under GLP practices, with appropriate documentation in place, it will also interact with external customers for which samples are processed, assuring that such communication is clear and disseminated in time, and processed samples are shipped back to customer, according to customer timeline. | 01/16/2025 |
| 1856 | Organogenesis Norwood, MA QC Analyst I-Cell Culture Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Cell Culture performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. The QC Analyst I performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 01/16/2025 |
| 1857 | Organogenesis Norwood, MA QC Analyst I - Chemistry Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Chemistry performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. Performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 01/16/2025 |
| 1858 | Orthofix Lewisville, TX Associate Quality Engineer - Operations B.S. Engineering degree or equivalent Exp: 0-2 years |
The Associate Quality Engineer engages with cross-functional team members and suppliers to drive Quality performance and to ensure that product quality meets all internal and external requirements. They will support initiatives to improve quality and customer satisfaction. The Associate Quality Engineer position also ensures compliance with Quality system and other standards and regulations, company quality requirements and corporate objectives. | 01/16/2025 |
| 1859 | Orthofix Carlsbad, CA Clinical Lab Associate Bachelor’s Degree Exp: 1 year |
Orthofix is looking for a Clinical Lab Associate (CLA) to join our team at our corporate headquarters in Lewisville, TX. As the Clinical Lab Associate you will be responsible for the successful execution and lab planning for all spine courses, HCP training, and internal stakeholder training. This includes working with Medical Education teammates, Marketing, R&D, Regulatory, and Compliance departments to facilitate hands-on surgical training and execute courses and given projects that are set forth by the Spine management. This position includes the utilization of equipment including audiovisual processes, inventory of lab supplies, (add “surgical) instruments, cadaveric specimens, and demo set shipments to the field and Spine office locations. In this role you will work daily with the Medical Education Events Team to coordinate and exceed lab attendees’ overall experience and expectations. This position is responsible for holding the Company, mission and objectives as guiding business principles, remaining in compliance with all safety and HCP protocols, and for driving constant and consistent quality improvement and industry best-practices. | 01/16/2025 |
| 1860 | DPT Laboratories (Viatris) San Antonio, TX Associate Scientist Q Bachelor’s degree in Life Science Exp: 0-2 years |
Testing of chemical components or products. Will involve the use of major laboratory instruments and equipment: HPLC, GC, FTIR, UV/VIS, as well as utilizing wet chemicals skills. Analytical review of data to ensure calculations is complete and accurate. Performs quantitative chemical analyses of APIs and related materials under direct supervision following established procedures and guidelines using laboratory instrumentation such as gas chromatographs, liquid chromatographs, ultraviolet-visible spectrophotometers, etc. Performs microbiological analysis as required. Treats numerical data throughout chemical analysis by performing mathematical calculations such as determining concentrations (molarity, parts per million, normality, etc.) and statistical information (standard deviation, mean, etc.). Prepares necessary reagents and equipment to expedite the performance of analysis by measuring and/or weighing chemicals, missing, and standardizing solutions, and assembling equipment. Maintains accurate records by logging samples received, recording samples analyzed, procedures used, and results obtained on datasheets and/or laboratory notebook. Weights and calculates samples in the physical and chemical analysis of products using balances and measured volumetric containers. Recognizes and informs Group Leader about daily lab activity and analytical problems. Organizes and properly labels samples, sample preparations, volumetric solutions etc. Perform other duties as assigned. | 01/16/2025 |
| 1861 | Mylan Pharmaceuticals (Viatris) Greensboro, NC Maintenance Technician Bachelor’s degree Exp: 1-2 years |
Perform daily and weekly tests of and coordinate maintenance on all facility life safety and fire suppression equipment, power and alternative power sources, interior and exterior light sources, and PIT equipment. Perform general painting and maintenance of warehouse interior and exterior, including but not limited to installation and repair of door hardware, drywall repair, storage rack repair or replacement, replacement of ceiling or carpet tiles, welding/grinding, plumbing fixture installation or replacement and light construction projects. Monitor and assist HVAC, refrigeration, fire protection, and fire alarm vendors and contractors when maintenance or repairs are being performed on equipment. Assemble and install furniture, furnishings, artwork, etc. as needed in the office and warehouse areas. Initiate, complete or file Trackwise Events and documentation as required. Issue, document and record Hot Work and Red Tag permits including coordination and communication with local emergency services providers during Red Tag events. Issue, document and record Lockout/Tag out events. Document and file Mylan Insurance Provider and Mylan EH&S department required records for NFPA inspections, life safety equipment and NCDENR required logs for property maintenance. | 01/16/2025 |
| 1862 | Mylan Pharmaceuticals (Viatris) Greensboro, NC Quality Technician, Inspections Bachelor’s degree Exp: 0-2 years |
Perform physical counts of outsourced products received. Prioritize and perform attribute inspections of outsourced products. Process product requisitions. Process returned goods and assign disposition. Create and maintain product specifications for outsourced products. Accurately compare product specifications with product. Process Notice of Rejections and TrackWise records for damaged products and returned goods. Collect temperature data for temperature monitored shipments. Operate forklift or related warehouse equipment as needed to perform job. Maintain and report departmental metrics. | 01/16/2025 |
| 1863 | Pacific BioLabs Hercules, CA Microbiology Laboratory Analyst II/III - Senior Analyst MS in Biology, Pharmaceutical Sciences, Biotechnology or equivalent - Microbiology degree preferred Exp: 1+ years |
PBL has an immediate opening for a fulltime onsite Microbiology Laboratory Analyst II/III or Senior Analyst, depending on experience, in the Microbiology Services Department. The Microbiology Laboratory Analyst II/III or Senior Analyst will report to the Director of Microbiology and will contribute to general and complex laboratory testing, sample management and laboratory maintenance. The Microbiology Laboratory Analyst or Senior Analyst is expected to participate with the team to meet Microbiology Services Department goals and perform routine and non-routine laboratory duties as directed. As a member of the PBL Microbiology Services team, the Analyst will make contributions to the growth of the department primarily through laboratory testing, training peers, validations, and support of the company’s continuous improvement initiatives and client needs. This position is client-facing, and the analyst must be quality focused and work in accordance with the PBL Quality Management System. | 01/16/2025 |
| 1864 | Pacific BioLabs Hercules, CA In Vitro Research Assistant I/II/III Bachelor’s Degree in a science-related field (e.g., Biological Sciences, Toxicology, Pharmacology) Exp: 1-3 years |
PBL has immediate openings for a Research Assistant I/II/III in the In Vitro Services Department. The Research Assistant reports to the Director, In Vitro Services. The In Vitro Research Assistant is a laboratory level job focusing on the development, optimization, and execution of a variety in vitro (i.e., cell-based and noncell-based) test methods. Successful candidates will be familiar with laboratory procedures including the use of analytical balances, calculating, and preparing dilutions, pipetting, measuring pH, documenting study activities, and analyzing/interpreting data. The In Vitro Research Assistant is expected to perform under minimal supervision. Research Assistants may also contribute to general laboratory operations including equipment maintenance and maintaining a clean and organized laboratory environment. | 01/16/2025 |
| 1865 | PacBio Menlo Park, CA Scientist I, Reagent Quality Control Master’s in a scientific discipline Exp: 1-2 years |
PacBio is seeking a driven, self-starter for the position of Reagent Quality Control (QC) Scientist. In this role, the QC Scientist is required to complete high quality work through QC assay execution from analytical assays (e.g., HPLC, fluorescent assays, etc.) to Use Test assays involving PacBio’s sequencing platforms. In addition, the individual will complete QC assay validation and transfer activities, execute stability studies, trend and interpret data, troubleshoot QC failures, and complete sustaining QC process improvements in the Reagent Manufacturing Organization. In this multi-faceted role, the ideal candidate is organized, independent, detailed oriented, process driven, quality driven, and skilled at problem solving. | 01/16/2025 |
| 1866 | Pacific Edge Diagnostics Hummelstown, PA Laboratory Technician Bachelor's degree in medical technology, chemical, physical, or biological sciences Exp: 1 year |
Pacific Edge Diagnostics USA, an innovative cancer detection testing company is seeking a talented Clinical Laboratory Technician to join its team. The Clinical Laboratory Technician's primary responsibility will be to perform molecular clinical testing (from specimen receipt through reporting patient results), as well as general lab maintenance. | 01/16/2025 |
| 1867 | Pall (Danaher) Cortland, NY Engineer I Bachelor of Science in Engineering required. Mechanical, Chemical, Materials or Industrial Engineering Exp: 1+ years |
In the role of Engineer I, you will have the opportunity to apply your skills in project management, research and principles of engineering to the planning, design, development, documentation, and testing/debugging of a variety of materials, components & finished goods in context of change management resulting from supplier obsolescence. his position is an onsite position and is located in Cortland, NY. | 01/16/2025 |
| 1868 | Pandorum Technologies San Carlos, CA Associate Research Scientist Master’s Degree in Life Sciences and related discipline Exp: 1 year |
Perform biochemical and cell-based assays, assay development, protein production and characterization, ELISA, western, biomarker studies and use various molecular biology tools. Work with a team of scientists towards establishing various protocols with high quality, generate reproducible SOPs compatible with cGMP process for technology/knowledge transfer for clinical grade production. Develop and optimize protocols for various cell and molecular biology studies, such as RNA preparation and RT-PCR. Protein production, purification, characterization and analysis by ELISA, SDS-PAGE, western, other biochemical techniques. Generate data for Company newsletter, website, social media, printed journals etc. Analyse data and prepare reports. Prepare SOPs for various experimental procedures. Prepare data for internal and external presentations, communications and publications. Participate in team meetings and scientific discussions | 01/16/2025 |
| 1869 | Paragon 28’ Englewood, CO Associate Product Sustaining Engineer Bachelor’s degree in Mechanical Engineering, Biomedical Engineering or related engineering discipline Exp: 0-3 years |
The Associate Product Sustaining Engineer works with direction from senior Engineering staff on projects that focus on legacy product systems and design and development of medical devices. | 01/16/2025 |
| 1870 | Paragonix Technologies Waltham, MA Associate Quality Engineer - Operations Bachelor’s Degree in an engineering or scientific discipline. Exp: 1 year |
As an Associate Quality Engineer, you will work closely with cross-functional teams to support various aspects of quality engineering, with a focus on New Product Introduction and failure analysis. Reporting to the Manager, Quality Engineering, you will assist in implementing and maintaining quality systems and processes to meet regulatory requirements and industry standards. | 01/16/2025 |
| 1871 | Paragonix Technologies Waltham, MA Quality Engineer Bachelor’s Degree in an engineering or scientific discipline. Exp: 1-3 years |
The Quality Engineer plays an integral role in Paragonix’s Quality Department as a hands-on engineering role conducting post market investigations of FDA approved medical devices. The position requires strong organization skills, attention to detail, ability to work in cross functional teams, and drive to accomplish departmental and company goals. | 01/16/2025 |
| 1872 | PCI Bedford, NH QC Microbiologist I BS/BA degree in Microbiology or related scientific field. Exp: 1 year |
The Microbiologist I conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures. Performs Lab work and other tasks as assigned by management. | 01/16/2025 |
| 1873 | PCI Madison, WI Validation Engineer I Bachelor’s degree in Engineering or related scientific discipline Exp: 1-3 years |
The Validation Engineer I performs an array of well-defined validation activities in support of cGMP pharmaceutical/medical device contract manufacturing across multiple PCI facilities. In collaboration with validation management, the Engineer I assist with internal project teams and external validation firms on validation/qualification initiatives and ensures project schedules are met. Complies with requirements of the Safety Program, including PCI Health and Safety mandates and OSHA requirements. In carrying out duties, contributes and promotes a positive and equitable working environment emphasizing the PCI Values: Customer Focus, Innovation, Integrity, Collaboration, and Superior Performance. | 01/16/2025 |
| 1874 | PCI Rockford, IL Operations Process Engineer Bachelor's Degree in a related field Exp: 1-5 years |
This position will work to continuously improve processes and systems that ultimately lead to improved profitability to the company. Using all available Engineering, Lean, and Six Sigma tools, this position will work independently and cross-functionally to drive out waste and reduce process variability. | 01/16/2025 |
| 1875 | PCI Rockford, IL RFD Microbiologist 1 Bachelor's Degree in a related field Exp: 1-5 years |
The primary function of this role is to perform basic tasks such as collect and process environmental samples from across all Rockford facilities using aseptic technique. In addition, this role is responsible for supporting basic microbiological functions and daily monitoring of the Laboratory temperature for various equipment in the Laboratory. This role may participate in training of other analysis in techniques for which competency has been demonstrated. There are no supervisory responsibilities associated with this role. | 01/16/2025 |
| 1876 | Penumbra Alameda, CA Manufacturing Engineer II, Operations Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing and business processes with interaction between production, cross-departmental engineering groups, and other cross-functional teams (such as Regulatory, Quality, R&D, Supply Chain, IT, etc.) in executing and coordinating business operations systems projects and activities. Essential job functions include creating and executing an integrated cross-functional project plan. | 01/16/2025 |
| 1877 | Penumbra Alameda, CA Quality Monitoring & Improvement Specialist I Bachelor's degree preferably in engineering, life sciences, or a related field Exp: 1+ years |
As a key member of the Quality team, you will have a hand in ensuring that Penumbra's life-saving products adhere to the highest standards of quality and safety. In the Quality Monitoring & Improvement Specialist I role, you will be supporting our Quality Management System (QMS) processes, specifically Corrective and Preventive Actions (CAPAs), Nonconformance Reports (NCRs) and Deviation Authorizations (DAs) following Penumbra's procedures and regulatory requirements. You will organize and host board meetings to facilitate board review of documentation supporting these systems. You will also assist with data compilation for monthly trending meetings. | 01/16/2025 |
| 1878 | LabCorp Phoenix, AZ Molecular Technologist Bachelor’s degree in Chemical or Biological science, Clinical Laboratory Science, Medical Technology Exp: 1 year |
Are you an experienced Clinical Lab Professional? If so, Labcorp wants to speak with you about exciting opportunities to join our team as a Technologist at the Sunshine Lab in Phoenix, AZ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at Labcorp: “Improving Health, Improving Lives”. | 01/16/2025 |
| 1879 | LabCorp San Antonio, TX Lab Technologist - Molecular Microbiology Bachelor’s degree in Chemical or Biological science, Clinical Laboratory Science, Medical Technology Exp: 1 year |
Are you an experienced Clinical Lab Professional? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist at in San Antonio, TX. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. | 01/16/2025 |
| 1880 | LabCorp Saint Paul, MN MCT Laboratory Technologist Trainee Bachelor's degree in chemical, biological or clinical laboratory science or medical technology. Exp: No exp |
Are you looking to embark on a new challenge? The possibilities are endless when start your career at Labcorp! We would love to discuss the exciting opportunities you will encounter when you join our team as a Technologist Trainee. In this position, you will work in a patient focused, fast paced, and inspiring environment. You will have a dynamic role in the fulfilment of Labcorp’s overall mission of “Improving Health, Improving Lives.” The MCT Department is looking for a Technologist Trainee to work in our laboratory. The candidate will receive on-the-job training for the pre-analytical through post-analytical set-up and testing of patient samples. This laboratory is responsible for screening blood, serum, urine and meconium sample types for drugs of abuse. We also perform Therapeutic Drug Monitoring (TDM) and STAT testing for local clinics and hospitals. The MCT Laboratory uses immunoassay methodology (Beckman Coulter AU5800 Chemistry analyzers) to test samples. Some assays require a chemical extraction before analysis. | 01/16/2025 |
| 1881 | LabCorp Madison, WI Research Assistant Bioanalytical -LCMS Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field Exp: 1+ years |
Do you have a strong background in LCMS? Are you wanting to apply your LCMS skills into improving the lives and wellness of people around the globe? Join Labcorp Biopharma as a Research Assistant in our Bioanalytical Metabolism Team in Madison, WI. Put your background with LC-MS Liquid chromatography and Mass Spectrometry focusing on large molecule sample analysis. We’re looking for a flexible, research and development focused individual who can think outside the box and is interested in bioanalysis of liquid and tissue matrices. As a Research Assistant in our Bioanalytical team you will provide assistance with experiments and with analytical and routine scientific procedures according to protocols. | 01/16/2025 |
| 1882 | LabCorp Madison, WI Lab Scientist Bachelor's degree in biology, chemistry, or related life science Exp: 1-2 years |
Labcorp Drug Development, the world’s most comprehensive drug development company, dedicated to improving healthcare and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow’s challenges as they evolve. We are looking for the right candidate to join our team in Madison, WI as a Lab Scientist! Come and be a part of helping many and fulfilling Labcorp's mission of improving health and improving lives! | 01/16/2025 |
| 1883 | LabCorp Greenfield, IN Sample Processing Technician Bachelor’s degree in Life Sciences such as Animal Science, Biology, Chemistry, Wildlife Studies or related field Exp: 1+ years |
Lab Sampling Technician-Study Tech position in our Greenfield IN location is responsible for the timely and accurate receipt, processing and storage of laboratory samples in compliance with GLP guidelines, study protocols and standard operating procedure, as well as managing the inventory of biological samples. | 01/16/2025 |
| 1884 | LabCorp Greenfield, IN Research Assistant (Study Tech) Animal Operations achelor’s Degree in Animal Science, Biology, Wildlife Studies, or related life science field Exp: 1-2 years |
Your work will contribute to improving the lives and wellness of both people and animals around the world. In this position you will be conducting Animal Research studies that will be looking at the safety, effectiveness and toxicity of drugs that are in early development phase and/or chemical substances. You’ll be maintaining the highest standards of animal care and welfare in accordance with Association for Assessment and Accreditation of Laboratory Animal Care International (AAALAC). Some of the most common tasks include performing various dosing techniques, may perform bleeding techniques, may collect biological samples, basic measurements such as body weight, food consumption, body temperature, blood pressure, etc. In this position your work will play a key role in bringing new scientific discoveries to life and make a difference in the lives of millions! | 01/16/2025 |
| 1885 | Pfizer McPherson, KS Process Engineer - Capital Engineering Bachelor's degree Exp: 0+ years |
The Capital Engineering Process Engineer is a key technical role responsible for providing engineering and process equipment expertise for the execution of Capital projects at the McPherson site. The role requires a high level of technical expertise in pharmaceutical processing systems, formulation equipment, high purity piping distribution systems, aseptic filling operations, terminal sterilization processes, inspection / packaging equipment, and clean room facilities design requirements. The incumbent will provide focused process ownership and the technical expertise to ensure high quality and efficient sterile injectable products. As technical lead, the Capital Engineering Process Engineer partners with supervision and production colleagues to identify and implement innovative solutions. This role focuses on developing new processes on site, resolving engineering issues, and providing technical support and troubleshooting during all phases of the Capital project. The Capital Engineering Process Engineer supports the Capital Portfolio Manager in the execution of assigned projects, which may include the coordination of internal company resources and vendors as part of the execution of projects. | 01/16/2025 |
| 1886 | NAMSA Irvine, CA Senior Laboratory Technician - Quality Control Bachelors degree Exp: 0 years |
May perform various testing independently in accordance with SOPs and utilizing applicable work instructions, standards or guidelines. Performs routine calculations and may participate in analyzing and interpreting results. Maintain all test equipment and supplies for various testing. Clean glassware and prepare reagents for use in laboratory testing. Perform routine disposal of laboratory waste including disposal of test articles. Assist with making solutions and preparing reagents.Assist in the preparation of items for testing. Monitor raw materials and final finished media for conformance with applicable material specifications and SOPs. May be responsible for extractions, which may include: test article and control preparation, animal holding and preparation and solution preparation. May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. Accurately collect and record raw data in logbooks and on worksheets. Maintain clean workspace, testing supplies, and equipment. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable and in accordance with criteria outlined in Standard Operating Procedures. May be required to operate specified laboratory equipment as applicable. Maintains an efficient workflow process relative to sample prioritization. Other duties as assigned. | 01/06/2025 |
| 1887 | Nanomix San Leandro, CA Associate Scientist, Assay Development Bachelor’s degree (or equivalent) in in Biology, Bioengineering, Chemistry, Chemical Engineering, or related field Exp: 0-2 years |
Nanomix has developed tests for the diagnosis of sepsis, acute kidney injury, and COVID-19, and is looking for an Assay Development Associate Scientist to help accelerate these programs and the development of other IVD assay products in the pipeline. This is an opportunity to work with a world class team to deliver an advanced, mobile medical diagnostic platform of urgent need to the healthcare industry. | 01/06/2025 |
| 1888 | NantWorks Culver City, CA Battery Technician Bachelor’s in a technical field Exp: 0-3+ years |
The Battery Technician is a key position within Research & Development that assists in building test cells to guide decision-making. They will be responsible for approaching cell engineering and fabrication with a high level of detail and integrity. The ideal candidate would be extremely flexible, curious, resilient, and eager to learn. | 01/06/2025 |
| 1889 | Natera Austin, TX Clinical Laboratory Operator Extractions BS/BA in a biological science or a related field Exp: 0-2 years |
This position assists in analyzing specimens and maintaining equipment in good operating condition to ensure accurate and timely testing of patient samples. This role involves adhering to Good Laboratory Practices (GLP), troubleshooting equipment malfunctions, providing guidance to new team members, and maintaining compliance with regulatory standards. The technician plays a crucial role in supporting laboratory operations, ensuring a clean and organized workspace, and contributing to continuous improvement initiatives. | 01/06/2025 |
| 1890 | Natera Austin, TX CQV Engineer II BS/BA in a biological science/biomedical engineering, similar field of study Exp: 1 year |
We are seeking a Commission, Qualification and Validation (CQV) Engineer II to support the commissioning and validation of laboratory and robotic equipment. The ideal candidate will have hands-on experience in writing and executing IQ, OQ, and PQ protocols to ensure compliance with regulatory and quality standards. | 01/06/2025 |
| 1891 | Natera Austin, TX Instrument Support Engr 2 BS/BA in a biological science/biomedical engineering, similar field of study Exp: 1-3 years |
The Instrument Support Engineer is responsible for the service and support of laboratory equipment and instrumentation utilized in the Operations laboratory. The scope of support includes installation, calibration, maintenance, and repair of both simple (e.g., plate sealers) and complex (e.g., liquid handling robotics) instrumentation in the laboratory. The Instrument Service Engineer will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. | 01/06/2025 |
| 1892 | LGC Remote/Alexandria, MN Field Application Scientist I Bachelor's or Master's degree in Molecular Biology, Biochemistry, Chemistry, Genetics, or related field required. Exp: 1-3 years |
The Field Service Application Scientist I is a multi-disciplinary molecular biology and organic chemistry position that will contribute to the organization as part of our Global Field Service team, bringing curiosity, problem solving skills, and scientific acumen to LGC. The Field Service team supports various wings of the organization such as Laboratory Operations, Engineering, Sales, and Manufacturing. | 01/06/2025 |
| 1893 | LGC Cumberland Foreside, ME Quality Control Technologist I Bachelor’s degree in Medical Technology (preferred) or related science degree (i.e. biology, chemistry, biochemistry) Exp: 1-3 years |
Follows standardized procedures and prepares samples for testing. Analyzes test results for accuracy, acceptability, and critical limits. Relies on limited independent judgment to plan and accomplish goals. Performs a variety of tasks. A limited degree of creativity and latitude is required. | 01/06/2025 |
| 1894 | LGC Milford, MA Manufacturing Associate Preferred Bachelor’s degree, with a concentration in Biology, Chemistry, or related science Exp: 1-3 years |
The Manufacturing Associate provides direct labor for the manufacturing of high-quality diagnostic products using manual and semi-automated equipment and prepares/completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 01/06/2025 |
| 1895 | LGC Novato, CA GMP Manufacturing Technician I/II/III - Synthesis Bachelor's degree in a related STEM field Exp: 1 year |
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management. This role will be on our Synthesis team in Novato Lab. | 01/06/2025 |
| 1896 | LGC Novato, CA GMP Manufacturing Technician I/II/III -KIT Lab Bachelor's degree in a related STEM field Exp: 1 year |
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management. This will be in our Kit Lab in Novato. Techs do final dry down (lyophilizatoin), column packing for purification, aliquoting and kitting of product. | 01/06/2025 |
| 1897 | LGC Remote/Petaluma, CA Field Application Scientist I Bachelor's or Master's degree in Molecular Biology, Biochemistry, Chemistry, Genetics, or related field Exp: 1-3 years |
The Field Service Application Scientist I is a multi-disciplinary molecular biology and organic chemistry position that will contribute to the organization as part of our Global Field Service team, bringing curiosity, problem solving skills, and scientific acumen to LGC. The Field Service team supports various wings of the organization such as Laboratory Operations, Engineering, Sales, and Manufacturing. | 01/06/2025 |
| 1898 | LGC Petaluma, CA Oligonucleotide Production Technician I - Purification Bachelor’s degree in a STEM discipline Exp: 0-2 years |
The Oligonucleotide Production Technician I - Purification will perform tasks associated with the purification of oligonucleotides in a high throughput, time sensitive manufacturing environment. | 01/06/2025 |
| 1899 | Nephron West Columbia, SC Microbiology Environmental Monitoring Trainer Bachelor’s degree with a science background Exp: 1-2 years |
Performs on-the-job, group, and one-on-one trainings with Environmental Monitoring (EM) program personnel. Coordinates and utilizes different departments and resources for task specific trainings. The EM Trainer is an expert on monitoring performed as an EM Technician I, II, and III. Assists with additional work duties or responsibilities as evident or required. | 01/06/2025 |
| 1900 | Neuralink Austin, TX Quality Assurance Specialist Bachelor of Science degree, preferably in a science, engineering, or quality-related discipline Exp: 1 year |
The Quality Assurance (QA) Specialist will work with Neuralink's teams to ensure that the appropriate governing body regulations are followed. This includes, but is not limited to, adherence to ISO standards, Good Laboratory Practices (GLP), clinical guidelines, manufacturing protocols, and quality control practices. | 01/06/2025 |
| 1901 | Neuralink Austin, TX Quality Systems Specialist Bachelor of Science in Engineering or a related field Exp: 1-2 years |
As a Quality Systems Specialist, you will work with teams across the Neuralink organization to resolve isolated and systemic problems through NCRs and CAPAs. You’ll identify ways to trend defects and issues for broader audiences and leadership. This role involves communicating and collaborating with different teams, such as R&D, manufacturing, product, etc., to maintain document/change management and data systems and ensure regulatory compliance with applicable standards. | 01/06/2025 |
| 1902 | Neuralink Fremont, CA Quality Systems Specialist Bachelor of Science in Engineering or a related field Exp: 1-2 years |
As a Quality Systems Specialist, you will work with teams across the Neuralink organization to resolve isolated and systemic problems through NCRs and CAPAs. You’ll identify ways to trend defects and issues for broader audiences and leadership. This role involves communicating and collaborating with different teams, such as R&D, manufacturing, product, etc., to maintain document/change management and data systems and ensure regulatory compliance with applicable standards. | 01/06/2025 |
| 1903 | Neurogene Houston, TX Associate Scientist, Analytical Development BS in Molecular Biology, Biochemistry, Cell Biology, or related field. Exp: 1 year |
Reporting into the Senior Scientist, Analytical Development, the Associate Scientist, Analytical Development plays a critical role in ensuring analytical work is executed consistent with product development timelines for Neurogene’s product pipeline. The candidate will perform routine sample testing according to standard operating procedures to support Process Development activities and process transfer to manufacturing. The selected candidate will have the ability to perform different laboratory techniques as well as superior written/oral communication skills, which are essential for success in this key role in a rapidly growing start-up. Furthermore, the candidate will be self-motivated and able to work both independently and within a collaborative team environment. | 01/06/2025 |
| 1904 | Neurona Therapeutics South SF, CA Research Associate Bachelor’s degree Exp: 1-2 years |
Neurona Therapeutics is a clinical stage biotechnology company based in South San Francisco, CA that was created to develop cell-based therapies for neurological disease. We have an opening for a Preclinical Research Associate who will contribute to ongoing programs and build new animal models to study modulation of neural circuits and support translational development of cellular therapeutics. | 01/06/2025 |
| 1905 | New England Biolabs Ipswich, MA Process Development Scientist I/II Bachelor’s or master’s degree in microbiology, biochemistry, biotechnology, or a related field. Exp: 1-4 years |
We are seeking a highly motivated and detail-oriented Process Development Scientist to join our Cloning & Fermentation Development Team at New England Biolabs (NEB). The successful candidate will play a crucial role in developing and optimizing processes for bacterial and yeast expression systems, contributing to the production of recombinant proteins for various applications. | 01/06/2025 |
| 1906 | NJ Bio Princeton, NJ Scientist, Process Development MS level in Organic Chemistry Exp: 0-2 years |
Under minimal supervision works on multiple steps/multiple projects to execute chemical syntheses from mgs to grams to kilo scales and conduct pilot scale synthesis (kilo scale), purification and characterization of compounds and present results and progress updates to internal and external stakeholders, stay abreast of current literature in scientific areas, maintain equipment, chemical inventory and lab support and Perform duties as required. The incumbent works cross-functionally with internal departments and external resources on process development related issues. The Scientist, Process Development supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 01/06/2025 |
| 1907 | Nkarta South SF, CA Cell Therapy Drug Product Engineer 2 – PD/MSAT Bachelor’s degree in chemical or biochemical engineering or related field Exp: 1+ years |
We are seeking a highly motivated and collaborative Engineer to join the Process Development/Manufacturing Science and Technology (PD-MSAT) team in developing and supporting Nkarta’s pipeline of cellular immunotherapy platform and products. This role will primarily represent CMC in our ongoing clinical operations and drug product development. Priorities will include investigations in support of drug product formulation/filling as well as drug processing characterization activities including technology transfer of drug product processing for clinical and future commercial programs. | 01/06/2025 |
| 1908 | Noah Medical San Carlos, CA Robotics and Controls Engineer M.S. in Mechanical, Controls, Robotics or related Engineering discipline Exp: 1 year |
The Robotics and Controls Team at Noah Medical is dedicated to the development and implementation of safe and high quality control algorithms and software. Comprising seasoned engineers with backgrounds in healthcare and other safety-critical industries, we collaborate with clinical, product, and hardware design teams to deliver user-centric solutions. Joining our team means becoming a part of a dynamic and passionate group dedicated to making a significant impact on the future of healthcare through groundbreaking technology. We are looking for a highly motivated, curious, and independent-thinking individual who is eager to take ownership and to contribute to revolutionizing the world of medical robotics while helping make Noah a great place to work. | 01/06/2025 |
| 1909 | Noah Medical San Jose, CA Test Technician BS in Computer Science, Electrical Engineering, or Industrial Engineering Exp: 1 year |
We are seeking a skilled Test Technician to join our team. The ideal candidate will be responsible for testing and troubleshooting medical robotic systems while adhering to Good Manufacturing Practices (GMP). The successful candidate will have a strong understanding of robotic hardware, sensors, motors, PLC’s, relays, circuit boards, computers, cabling and experience with and testing, excellent troubleshooting skills, and GMP experience. | 01/06/2025 |
| 1910 | Nortech Systems Bemidji, MN Quality Engineer Bachelor's degree Exp: 1-2 years |
Are you seeking a role that supports the delivery of lifesaving devices? Do you enjoy working with cross-functional teams to ensure quality standards are met throughout the production process? Are you interested in a role that Identifies quality issues, recommends solutions, and implements changes to resolve discrepancies? Do you like the rigor of Ensuring that processes adhere to quality standards and regulatory requirements. If any of these resonate with you, we encourage you to explore our Quality Engineer role! | 01/06/2025 |
| 1911 | NorthEast Biolab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: Entry Level |
Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance. Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage. Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials. Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit. Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records. Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices. Follow appropriate safety and study requirements by reading, understanding, and following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) requirements, and Sponsor Study protocols. Support business development and marketing activities, foster client relationships, and help onboard new sponsors | 01/06/2025 |
| 1912 | NorthStar Medical Radioisotopes Beloit, WI Quality Control Analyst Bachelor’s Degree in Chemistry, Biology, or other related scientific discipline Exp: 1 year |
The primary role of this position is to conduct and validate various biological and analytical quality control assays associated with the processing of radiopharmaceutical isotopes and drugs to ensure compliance with established standards. This role requires extensive training on radiation safety including ALARA (“as low as reasonably achievable”) principles. The Senior Quality Control Analyst will lead various activities, as further described below. Duties will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. | 01/06/2025 |
| 1913 | NorthStar Medical Radioisotopes Beloit, WI Radiopharmaceutical Manufacturing Associate Bachelor's Degree in a STEM discipline Exp: 1 year |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. | 01/06/2025 |
| 1914 | Novavax Gaithersburg, MD Associate Scientist, Downstream Process Development Master's degree in Bio/Chem Engineering, Biology, Chemistry, Pharmaceutical Science, Biochemistry, biophysics, Molecular Biology, Life Sciences, vacci Exp: 1+ years |
We are seeking an Associate Scientist to join our Downstream Process Development group in Gaithersburg, MD. Qualified individuals will be responsible for hands-on execution of downstream chromatography and filtration processes in support of process development, scale-up, process characterization activities, and technical support of cGMP manufacturing for proteins, nanoparticles, and virus-like particle (VLP) based vaccines. The candidate will ensure scientifically sound experimental execution, analysis, and reporting. The candidate will be responsible for drafting technical development reports summarizing critical data. The candidate is expected to be highly self-motivated, well organized, and an innovative thinker focused on execution with a sense of urgency. This position will be located at our Gaithersburg, MD facility | 01/06/2025 |
| 1915 | Noven Miami, FL QC Analyst Bachelor’s Degree (BA/BS) in Chemistry or related field Exp: 1 year |
The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 01/06/2025 |
| 1916 | Novitium East Windsor, NJ Quality Control Analyst Bachelors in Pharmaceutical Sciences / Biology / Chemistry / Microbiology / Chemical / Related Exp: 1 year |
Quality Control Analyst (East Windsor, NJ) (Multiple Openings) Conduct research, analysis, synthesis, and experimentation on substances, for such purposes as product and process development and application, quantitative and qualitative analysis, and improvement of analytical methodologies; conduct testing and analysis of pharmaceutical raw materials like drug substance, excipients and packaging materials to analyze various parameters like assay, dissolution, impurities, related substances, residual solvents using various technical instruments like HPLC, GC, UV spectrometry; Conduct testing and analysis of finished product for different dosage forms like capsules, tablets, powder for oral suspension and solutions. The dosage forms include food supplements like vitamin capsules, mineral tablets, and multivitamin syrups. | 01/06/2025 |
| 1917 | Novitium East Windsor, NJ Instrumentation Engineer Bachelor’s in Instrumentation / industrial / electronics / electrical / mechanical / related Exp: 6 months |
Instrumentation Engineer (East Windsor, NJ) (Multiple Openings) Responsible for Instrument and Equipment’s of entire Plant; Installation, troubleshooting & calibration of instruments such as TOC Analyzer, HMI, PLC, Flow Meters, Temperature controller, transmitter, pressure transmitter, gas analyzer; Maintaining minimal instrument downtime through troubleshooting & maintenance activities; Maintaining data backup, instrument documentation, and Spares Inventory & Annual Maintenance contracts; Pro-active Support for Quality Control, Production & Compliance group’s activities; Follow-ups and closures of instrument Change controls, deviations instrument related incidents, & CAP A (corrective and preventive action); Procurement of qualified equipment’s as per GLP & Pharmacopeia requirements, and responsible for IQ, OQ, DQ and PQ for instruments and manage all paperwork. | 01/06/2025 |
| 1918 | Novo Nordisk Boulder, CO Research Associate - Chemical Development BA/BS or master’s degree in chemistry, Biology or related field Exp: 0 years |
Novo Nordisk Global Nucleic Acid Therapies (GNAT) is seeking highly motivated scientists to join its CMC Chemical Development team in Boulder, Colorado. The candidate will be expected to be a key technical resource developing innovative solutions for scalable syntheses, work-up, purifications, and isolations of oligonucleotides, establishing improvements in purity, yield, reproducibility, throughput and environmental impact. The successful candidate will ideally have a strong organic chemistry understanding with exposure to principles of process development, optimization, scale up and tech transfer into a manufacturing setting. This position will support therapeutic programs in multiple disease areas and will contribute to the development of scalable processes supporting Novo Nordisk oligonucleotide programs. Qualified candidates will be expected to work well in a collaborative team environment and be able to independently execute research across a wide range of oligonucleotide and organic chemistry projects. | 01/06/2025 |
| 1919 | Novo Nordisk West Lebanon, NH Manufacturing Technician Bachelors’ Degree in a science discipline Exp: 0 years |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 01/06/2025 |
| 1920 | Novo Nordisk West Lebanon, NH Quality Assurance Area Specialist II Bachelor’s Degree (or equivalent) required, a scientific discipline Exp: 1-3 years |
This position is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Will be a QA presence on the manufacturing floor. | 01/06/2025 |
| 1921 | Novo Nordisk West Lebanon, NH Quality Assurance Area Specialist I Bachelor’s Degree (or equivalent) required, a scientific discipline Exp: 1 year |
This position will review manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Will assist in the internal audit program and be a QA presence on the manufacturing floor. | 01/06/2025 |
| 1922 | OraSure Bethlehem, PA Manufacturing Technician (2nd shift) Bachelors degree Exp: 1-3 years |
Operate semi-automated and automated equipment in the production area at a sufficient rate and quality level. Perform on-line inspection of all components/parts produced. Take corrective action and/or make recommendations to the supervisor. Complete all paperwork and equipment logbooks and review other operator's paperwork for accuracy and completeness as required. Responsible for set-up and shutdown of equipment and work closely with the maintenance department in identifying maintenance and repair needs on the equipment. Provide cross training to operators on all pieces of equipment in the production area. Must follow all GMP and company safety regulations and guidelines. May assist in validation of equipment and be solicited for input into development and manufacturing process improvements. | 01/06/2025 |
| 1923 | Nucleus Radiopharma Rochester, MN Quality Control Technician Bachelor’s degree in chemistry, biology required Exp: 1 year |
The Quality Control (QC) Technician performs assigned laboratory testing in compliance with applicable standard operating procedures (SOPs) and in compliance with U.S. and international regulatory requirements, including FDA, ISO, USP, and NRC guidelines. The QC Technician adheres to current good manufacturing practices (cGMP) and good documentation practices (GDocP) for all analyses. Working collaboratively with other laboratory personnel, the QC Technician coordinates instrument usage and completes laboratory tasks efficiently. The QC Technician completes testing and promptly reports any aberrant results to quality management. They work independently under limited supervision and handle radioactive materials as part of their duties. | 01/06/2025 |
| 1924 | Obsidian Therapeutics Bedford, MA Senior Research Associate, Analytical Development Contractor (Core Testing/Characterization) Masters in immunology/biomedical sciences or a related field Exp: 1+ years |
We’re looking for a highly motivated scientist with experience in primary human cell culture, molecular analytics, and cell-based assays to work with our Analytical Development Core Testing team. You’ll focus on characterizing engineered cell therapy products and supporting Obsidian’s tumor infiltrating lymphocytes (TIL), viral vector and critical materials analytical teams. You’ll support critical studies and experiments to advance Obsidian OBX-115 product understanding and work with various subject matter experts across different functional groups, affording a significant learning opportunity and career development. This position is a six month contract role. | 01/06/2025 |
| 1925 | Ocugen Malvern, PA Clinical Trial Associate BA/BS degree, preferably in life sciences. Exp: 1+ years |
The Clinical Trial Associate supports the operational execution of clinical studies. This individual will be responsible for the successful delivery of clinical studies including conducting LDNA tests for clinical studies according to agreed cost and timelines while ensuring patient safety and data integrity and quality. | 01/06/2025 |
| 1926 | Masimo Irvine, CA Engineer, Failure Analysis Bachelor’s degree, preferably in Electrical Engineering, or equivalent Exp: 0-1 years |
Responsible for performing failure analysis of customer returned products, newly manufactured products, and prototype products, with the intent of root cause isolation of full device system issues or sensor and cable issues down to the circuit board, component, or process level. Works closely with Compliance, Regulatory, R &D Engineering, Operations and QA at various levels within the organization to understand the root cause of product failures and identify product improvements | 12/30/2024 |
| 1927 | Masimo Irvine, CA Clinical Research Associate Bachelor’s degree, preferable in Science or in a related field is required Exp: 1-3 years |
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. This position must ensure that all activities will be conducted in accordance with Government Regulations (FDA, MDD and International), Good Clinical Practices (GCP) and Department Operating Procedures (DOP). | 12/30/2024 |
| 1928 | MaxCyte Rockville, MD Software Engineer B.S. in Computer Science, Computer Engineering, or Electrical Engineering Exp: 0-3 years |
Join MaxCyte as a Software Engineer and be at the forefront of developing cutting-edge instrument software and applications, including intuitive UIs and advanced instrument control layers. You’ll be involved in every stage of the software lifecycle, from initial concept to final commercialization, ensuring our life sciences tools are best-in-class. This role offers a unique opportunity to work on innovative projects that make a real impact in the world of biotechnology. Additionally, as a key member of a high-performing team, you’ll have ample opportunities to learn and grow, staying updated with the latest technologies and industry trends. | 12/30/2024 |
| 1929 | MaxCyte Rockville, MD Electrical Engineer B.S. in Electrical Engineering (M.S. preferred) Exp: 0-3 years |
Join MaxCyte as an Electrical Engineer and be at the forefront of developing cutting-edge instrument electronics, including high-speed/high-voltage systems, power electronics, data acquisition, signal processing, and start-of-the-art sensors. You’ll be involved in every stage of the instrument lifecycle, from initial concept to final commercialization, ensuring our life sciences tools are best-in-class. This role offers a unique opportunity to work on innovative projects that make a real impact in the world of biotechnology. Additionally, as a key member of a high-performing team, you’ll have ample opportunities to learn and grow, staying updated with the latest technologies and industry trends. | 12/30/2024 |
| 1930 | Meadowhawk Biolabs Marlborough, MA Research Associate I LCMS Bionanalysis Bachelor’s degree in chemistry, biochemistry, pharmaceutical sciences, or another related scientific field Exp: No Exp |
Meadowhawk Biolabs is seeking a highly motivated and dynamic Research Associate to work within the Discovery Bioanalytical Team at our Marlborough, MA location to perform LC-MS/MS assays in a fast-paced team environment. The ideal candidate is driven, hardworking, willing to learn, dedicated, and passionate about science. Given that we are a newly launched Contract Research Organization (CRO) founded by an experienced team of industry veterans, this ground floor position offers unique opportunities for the successful candidate to contribute meaningfully to the creation and development of our services, expand their knowledge base by participation in multidisciplinary teams, and advance their career in capabilities and responsibilities. | 12/30/2024 |
| 1931 | Meadowhawk Biolabs Marlborough, MA Research Associate II, LCMS Bioanalysis Bachelor’s degree in chemistry, biochemistry, pharmaceutical sciences, or another related scientific field Exp: 1 year |
Meadowhawk Biolabs is seeking a highly motivated and dynamic Research Associate II to work within the Discovery Bioanalytical Team at our Marlborough, MA location to perform LC-MS/MS assays in a fast-paced team environment. The ideal candidate is driven, hardworking, willing to learn, dedicated, and passionate about science. Given that we are a newly launched Contract Research Organization (CRO) founded by an experienced team of industry veterans, this ground floor position offers unique opportunities for the successful candidate to contribute meaningfully to the creation and development of our services, expand their knowledge base by participation in multidisciplinary teams, and advance their career in capabilities and responsibilities. | 12/30/2024 |
| 1932 | Medpace Irving (Dallas), TX Clinical Data Coordinator - Biology Degree Bachelor's degree in a Life Science or related field Exp: Entry Level |
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves working on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your knowledge and experience to further develop and grow your career even further, then this is the opportunity for you! | 12/30/2024 |
| 1933 | Medpace Irving (Dallas), TX Clinical Data Coordinator - Chemistry Degree Bachelor's degree in a Life Science or related field Exp: Entry Level |
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves working on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your knowledge and experience to further develop and grow your career even further, then this is the opportunity for you! | 12/30/2024 |
| 1934 | Medpace Irving (Dallas), TX Clinical Data Coordinator - Mathematics Degree Bachelor's degree in a Life Science or related field Exp: Entry Level |
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves working on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your knowledge and experience to further develop and grow your career even further, then this is the opportunity for you! | 12/30/2024 |
| 1935 | Medpace Irving (Dallas), TX Clinical Research Project Coordinator - Entry Level Bachelor's degree in a Life Science or related field Exp: Entry Level |
Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology and more. If you are looking for a fast paced, collaborative work environment in clinical research and want to develop your career even further, then this is the opportunity for you. Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and hands on learning experience, especially for those without previous clinical research experience. | 12/30/2024 |
| 1936 | Medpace Cincinnati, OH Senior Data Scientist Master’s degree in informatics, computer science/engineering, health information, statistics, or related field Exp: 1-2 years |
We are currently seeking an experienced data scientist to join our Informatics team who will lead advanced analyses of methodological data to inform study design decisions. The Informatics team utilizes informatics principles and techniques to architect, mine, analyze, and visualize clinical trial data to inform study design choices for pharmaceutical development. The informaticist will create predictive data models to identify and analyze patterns, then program compelling visualizations of the data to support feasibility strategies. The team is seeking an experienced candidate for a senior-level position to contribute new skills to our team, sopport team growth and foster fellow analyst development. | 12/30/2024 |
| 1937 | Medtronic Fridley, MN Process Engineer II Master's degree in Engineering Exp: 0 years |
The Rice Creek Pharma Operations Advanced Manufacturing Engineering Process Engineer II is responsible for evaluating, improving, and controlling the overall performance of manufacturing areas that provide implantable components and finished devices, including combination products. This role involves leading and collaborating closely with Operations, Quality, Reliability Engineering, and Regulatory Affairs. The Process Development Engineer plays a crucial role in introducing new processes into manufacturing and providing technical solutions to product performance issues. | 12/30/2024 |
| 1938 | Medtronic Tempe, AZ Materials Engineer II Master's degree in Engineering Exp: 0 years |
Engineers are indispensable to achieving our Mission. That’s why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship, and the guidance you need to continue to develop your expertise. As a Materials Engineer II, you will be responsible for performing physical analysis of electronic components and medical devices, developing analysis techniques, and supporting analysis tools in a laboratory setting. You will have hands on responsibilities on multiple tools and you will collaborate across multiple engineering disciplines. | 12/30/2024 |
| 1939 | Medtronic Brooklyn Center, MN Quality Engineer II Master's degree in Engineering Exp: 0 years |
The Brooklyn Center facility also known as Medtronic Electronics Components Center (MECC) supports the production of components used in devices for a variety of Medtronic Operating Units (OUs). This role reports to the Operations Quality Manager at MECC. Key aspects of this role include executing the disposition and closure of nonconformances in a timely fashion, collaborating with customer sites (downstream Medtronic facilities) on non-conformance investigation and resolution, participating in a culture of collaboration and compliance in one of the Components Focus Factory (Includes Connectors/Molding, Capacitors, TDCO, and Feedthroughs), execute day to day operations, and execute continuous improvement/programmatic savings initiatives to reduce the overall quality risk within a specific Focus Factory. | 12/30/2024 |
| 1940 | Medtronic Los Angeles, CA Electrical Engineer II Master's degree in Electrical Engineering Exp: 0+ years |
In this exciting and challenging role as a test engineer, your responsibilities will include Designing, developing, and implementing testing methods and equipment. Plans and arranges schedules, and equipment required for verifying products. Provides test area with parameters for sample testing and specifies tests to be performed. Compiles data and defines changes required in testing equipment, testing procedures, manufacturing processes, or new testing requirements. Responsible for writing verification test plans and reports. This will be a hybrid position which requires person to be on site for test method development and supervising of product verification testing. | 12/30/2024 |
| 1941 | Medtronic Brooklyn Center or Minneapolis, MN Battery Manufacturing Engineer II Master's degree in Engineering Exp: 0 years |
In this exciting role as a Battery Manufacturing Engineer II at Medtronic’s Energy & Component Center (MECC), you will have responsibility for supporting and improving the manufacturing of the high quality batteries used in implantable medical devices. You will be responsible for day to day production support, new process development support and lead improvement projects. The Brooklyn Center facility supports the design, development, and production of components used in implantable devices for a variety of Medtronic businesses. In this role you will gain experience with products across Medtronic’s portfolio, supporting your development and growth. This role is responsible for improving manufacturing quality, lead time and cost through active problem solving, developing solutions and implementing process changes in accordance with the quality system. What does it take to be a leader at Medtronic? We look for inspiring and inclusive leaders who partner with others, knowing that diverse talent, skills, and perspectives lead to better outcomes. Please note this role does work on-site in the manufacturing area. | 12/30/2024 |
| 1942 | Medvacon Winchester, KY QC Analyst Bachelors degree in Chemistry, Biology, Chemical Engineering or Life Sciences Exp: 0-5 years |
A QC Analytical chemist is an entry level position for individuals who use their understanding of science to perform the basic and critical experimental work of day-to-day analysis, including generation and analysis of data. Their work is “hands on” in an analytical lab and requires analytical testing, computer operating, record keeping, and report writing abilities. This position performs the quality testing needed for raw material, in-process, finished goods, stability, and cleaning validation analysis. | 12/30/2024 |
| 1943 | Meissner Camarillo, CA R&D Scientist I Bachelor’s degree required in STEM-related field Exp: 1-5 years |
At Meissner, we provide B2B technical solutions, that are deployed to improve the human condition. Our customers use our products and technologies to develop new therapeutics and many familiar products that support our modern lifestyle. At the core of these products, are in-house technologies that are developed and maintained by highly talented and self-driven engineers and scientists. Projects are typically heavily weighted towards chemical processes and materials science at an R&D/prototype scale to pilot and production scales. The R&D Scientist will undertake independent research projects and/or investigations or be responsible with specific parts of larger projects, with a higher degree of independence. | 12/30/2024 |
| 1944 | Merck West Point, PA Assoc. Scientist, Analytical R&D Bachelor’s degree or higher in biology, chemistry, biochemistry, bio-engineering or related sciences Exp: 1 year |
We are seeking a growth and improvement minded Associate Scientist that can help drive our Strategic Operating Priorities working as a Subject Matter Expert with live virus vaccine potency assays. We are seeking a highly motivated colleague to join our team as a scientist supporting our inline and pipeline vaccine programs. This position will work in a GMP environment and will be expected to execute various cell-based assays in a high throughout environment. The candidate will work with a large team of colleagues to deliver high quality results for multiple vaccine products. This position will require work with various instrumentation to develop new methods in line with current technologies. | 12/30/2024 |
| 1945 | Merck West Point, PA Scientist, Laboratory Animal Resources Bachelor's degree Exp: 1+ year |
Our company a global healthcare leader, is currently seeking an Entry-Level Laboratory Animal Resources Associate to join our collaborative, dynamic, and inclusive Laboratory Animal Science Team at the West Point location. The successful candidate will be integral in planning, designing, and executing in vivo ophthalmology research, as well as some routine veterinary and animal colony management tasks. On-site and hands-on study-related lab work will be a crucial part of the role. The role also requires rotation weekend work and the ability to apply sound technical skills to assigned tasks, often with minimal supervision. | 12/30/2024 |
| 1946 | Meridian Bioscience Memphis, TN Quality Assurance Associate Bachelor’s degree in life science, chemistry, pharmaceutical science, statistics, or health/human services related field. Exp: 0-5 years |
The Quality Assurance (QA) Associate will support QA processes, programs, and conduct QA activities. This position will uphold standards, methods, and procedures for all stages of production. This position will identify continuous process improvement areas, in compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GLP) processes and documentation for quality control activities. This requires excellent technical skills and abilities, analytical and mathematical skills, organizational and time-management skills, verbal, and written communication skills, plus ability to apply attention to detail. | 12/30/2024 |
| 1947 | Meridian Bioscience North Billerica, MA Quality Control Technician Bachelor’s degree in a life science (Biology, Microbiology, etc.) Exp: 0-2 years |
Responsible for ensuring materials, processes, and products meet the required specifications, which involves, but is not limited to, inspections, metrology testing, documentation, and labeling reviews. Product acceptance or rejection. Responsible for maintaining equipment calibration. | 12/30/2024 |
| 1948 | MethodSense Morrisville, NC Quality and Safety Engineer Bachelor’s degree in biomedical engineering or alternative engineering degree. Exp: 1-7 years |
We are looking for talented Quality and Safety Engineers to join our experienced team. If you can commit yourself to supporting a passionate regulatory affairs and quality assurance business dedicated to their clients, you can have a career with us. We need someone with honesty, integrity and excellent communication and interpersonal skills. The position requires the ability to work with client company executives, test labs and FDA regulators. It also requires agility and love for knowledge. If you want to join a high energy purposed team, please apply. | 12/30/2024 |
| 1949 | Minaris Regenerative Medicine Mountain View, CA QC Analytical Associate I BA/BS in a science or relevant field required Exp: 0-2 years |
The Quality Control Analytical Associate serves as a support role to clinical and commercial production. The QC Analytical Associate will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. | 12/30/2024 |
| 1950 | Minaris Regenerative Medicine Allendale, NJ QA Associate II BS or higher education degree in a scientifically related field Exp: 1-3 years |
The Quality Assurance Associate plays a pivotal role in ensuring that all quality assurance activities are conducted efficiently and accurately. Under direct supervision, the associate supports daily tasks that are essential for maintaining and improving quality systems and adhering to client-specific procedures. Key responsibilities include document management, review of manufacturing batch records, quality control (QC) data, facilitating material releases, overseeing final product releases, and providing essential assistance to the Quality Management as needed. | 12/30/2024 |
| 1951 | Modulo Bio San Diego, CA Stem Cell Scientist MS in Genetics, Molecular Biology, Developmental Biology, Biochemistry, Regenerative Medicine, Neuroscience, or related field Exp: 1+ years |
Modulo Bio is seeking a Stem Cell Scientist to develop and scale an induced-pluripotent stem cell (iPSC)-based in vitro model of the neuroimmune system. Modulo Bio is building a proprietary immune cell modeling platform, which incorporates human genetics, functional genomics, molecular biology, cellular and tissue profiling, disease model engineering, and advanced computational models. The successful candidate will build a complex cell model platform with the goal of improving our understanding of human biology and therapeutic interventions to inform early and late stage pipeline efforts. Candidates with an eagerness to work within a highly leveraged, team-driven, dynamic research environment will be prioritized. The candidate will work in close collaboration with our internal Computational Biology group which is focused on next-generation sequencing (NGS), functional genomics, cell or tissue profiling, and bioinformatics analyses of cutting-edge large-scale genetic screening or single-cell technologies to enhance our analytic capabilities and to reveal the underlying mechanisms of human disease. | 12/30/2024 |
| 1952 | Molecular Assemblies San Diego, CA Research Associate II / Associate Scientist- Biochemistry M. S. in Biochemistry, Chemistry, Molecular Biology, or a related field. Exp: 1+ years |
The R&D organization is seeking a highly motivated and detail-oriented Associate Scientist to join the biochemistry team. In this role, you will work closely with senior scientists to support the development of high-fidelity, template-independent enzymatic synthesis of nucleic acids. The ideal candidate will have a foundational understanding of enzymology and kinetics and laboratory experience in biochemical assays. We are looking for someone who thrives in a fast-paced environment and is passionate about scientific discovery and innovation. This role is onsite 5 days a week. | 12/30/2024 |
| 1953 | Molecular Designs Birmingham, AL Lab Technician- Night Shift Bachelor’s degree in Biology, Chemistry, Biochemistry Exp: 6 months |
We're looking for a Molecular Lab Technician (MLT) to help with day-to-day screening procedures for our molecular testing laboratory. We’re seeking a highly driven, motivated, and experienced Lab Technician that understands the PCR process, its importance, and work through each complex step with the upmost efficiency. The ideal Lab Technician will have patience, empathy, time management, and professionalism with patients, co-workers, and providers. | 12/30/2024 |
| 1954 | Molecular Designs Birmingham, AL Quality Assurance Specialist Bachelor’s Degree in biology or related sciences preferred Exp: 1-2 years |
The Quality Assurance Specialist is responsible for supporting the Manager of Quality with implementing and maintaining all aspects of the quality management system. This position requires a person to perform various tasks (but not limited to) within the quality department including Documentation Control (manual and electronically), Corrective Actions, Nonconforming Product, assist with creation of Device Master Records, control of Device History Files, Quality Metrics and SOP/Work Instruction Development. | 12/30/2024 |
| 1955 | Moog Buffalo, NY Development Electrical Engineer Master’s Degree in Engineering Exp: 1+ years |
The Test Systems Electrical Development Engineer will contribute to the analysis, conceptual design, development, and test of complex control systems' electrical components. These systems will be used for qualification and acceptance testing of Moog's military aircraft control system products. The products of Moog generally are unique for each customer. Therefore, most new applications require a special, tailored design, even though adaptation of existing designs always are considered where appropriate. The Development Engineer will operate as part of a multi-disciplinary design and development team. You may coordinate the work of drafters, technicians, vendors, and others who support new designs. In the early stages of a new program, the project team will consult with the customer, establish the problem statement, conceive of potential hardware solutions to the problem, and then create a successful technical proposal. Under the technical direction of the team's lead Engineer, the Development Engineer will then contribute to the evolution of the conceptual design, technical project planning, detail design, and testing (risk mitigation, integration, and validation/verification). | 12/30/2024 |
| 1956 | Moog Salt Lake City, UT Research & Development Engineer Bachelor’s degree (B.S.) in related electromechanical, biomedical engineering, or technical discipline Exp: 1 year |
As a R&D Engineer you will perform engineering verification and validation testing activities within FDA QSR standards with guidance of senior engineering. Reporting to the Manager Senior, Engineering you will be located in Salt Lake City, Utah. | 12/30/2024 |
| 1957 | Novartis Morris Plains, NJ Cell Processing Specialist I Bachelor’s degree in relevant Engineering or Scientific discipline Exp: 1 year |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. The CPS I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 12/30/2024 |
| 1958 | Novartis Morris Plains, NJ Associate Scientist, Raw Materials Bachelor’s degree or MS in Biology, Chemistry, Biochemistry, Microbiology or other related science Exp: 1 year |
Under general direction; the Associate Scientist, Raw Material will direct and assist in functions supporting QC raw materials. | 12/30/2024 |
| 1959 | Novartis East Hanover, NJ Expert - Molecular Biology M.S. in Molecular Biology or closely related discipline Exp: 1 year |
As a key member of the Analytical Development team, this individual will support developmental activities to aid in delivering gene therapy to patients. The successful candidate will support technical and development projects designed to characterize gene therapy products through an assortment of analytical methods. This role will also contribute to cross-functional activities including monitoring and characterizing of processes and products to identify opportunities for continuous improvement. Growth mentality and passion to serve patients, his/her technical team and development programs is a must. | 12/30/2024 |
| 1960 | Novartis Millburn, NJ Production Technician I Bachelor’s degree in relevant Engineering or Scientific discipline Exp: 1+ years |
Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. | 12/30/2024 |
| 1961 | Novartis Indianapolis, IN Production Technician I Bachelor’s degree in relevant Engineering or Scientific discipline Exp: 1+ years |
Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. | 12/30/2024 |
| 1962 | Novartis Durham, NC Bioprocess Technician/Engineer (Upstream Nights) Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field Exp: Entry Level |
The BioProcess Technician or Engineer I/II/III is responsible for assisting with organizing, running, and sustaining the manufacturing operations process at the plant/site. The level of the role will be determined by the years of relevant experience. Novartis Gene Therapies is dedicated to developing and commercializing gene therapies for patients and families devastated by rare and life-threatening neurological genetic diseases. | 12/30/2024 |
| 1963 | Novartis Morris Plains, NJ QC Microbiology Technician Bachelor’s in Microbiology or closely related field Exp: 1 year |
The QC Microbiology Technician is responsible for assisting routine and batch-related Environmental Monitoring in controlled environments, following current Good Manufacturing Practices. | 12/30/2024 |
| 1964 | Myomo Burlington, MA Quality Engineer II Bachelor's degree in a related Engineering discipline Exp: 1+ year |
The Quality Engineer provides support to the QC Engineering Manager and team. The core aspects of this role are to focus on non-conforming materials, establish effective inspection methods, resolve supplier quality issues, and collaborate with Product Development to deliver effective product testing, validation, and inspection.He/she will also assist in the implementation of appropriate systems, policies, and procedures to ensure quality and compliance and proactively develop improved processes. The ideal candidate is a well-organized, process-oriented, and systematic-minded professional who is able to keep an eye toward process improvements and innovation. Keys to success in this role include the ability to demonstrate attention to detail as well as the capability to both collaborate effectively and work independently. He/she will be able to understand and incorporate the viewpoints of cross-functional stakeholders. | 12/30/2024 |
| 1965 | Myriad Genetics Salt Lake City, UT Lab Technologist II - Precise Lab Bachelor’s, or Master’s degree in medical technology or a chemical, physical, biological Exp: 6 months |
The Lab Technologist II is responsible for conducting laboratory processes that support specimen processing and testing. This position works with department management and quality team members to ensure that laboratory activities are defined, documented, and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation, and continuous improvement projects. | 12/30/2024 |
| 1966 | KVK Tech Newtown, PA QA Technical Reviewer Bachelor’s degree in Chemistry or a related field preferred Exp: 1-2 years |
The QA Technical Reviewer will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. | 12/16/2024 |
| 1967 | Kyowa Kirin Sanford, NC Project Engineer I Bachelor’s degree in engineering Exp: 1 year |
The Project Engineer will play a key in the design, construction, and start-up of a new manufacturing facility. Working directly with the Site Head during the project phases, the Project Engineer will transition into an operational role within the plant. This role will partner closely with the Site Leadership Team, gaining a comprehensive understanding of various functions and managing a range of projects to build both depth and breadth of experience across the site. This position will provide hands-on involvement in designing, developing, and operationalizing the facility from the ground up. | 12/16/2024 |
| 1968 | Leidos Remote, Transmission Reliability Engineer Bachelors in Electrical Engineering or related engineering degree is required Exp: 0+ years |
Leidos Engineering is seeking a Transmission Reliability Engineer to join our System Planning team. This role will involve the execution of transmission planning, transmission system modeling, compliance verification, and protective device coordination, as project and client criteria dictate. Successful candidates can expect to conduct Transmission system software modeling and analysis studies for Municipal Utilities, Investor-Owned Utilities, and Regional Planning organizations. The position will involve some degree of client-facing work, with some business development activities to be expected. The growth potential of this position is significant for a well-qualified candidate. | 12/16/2024 |
| 1969 | Leidos Pittsburgh, PA Associate Distribution Engineer Bachelors of Science in Engineering degree or Master’s degree (EE or CE preferred) Exp: 0+ years |
The successful candidate will have an interest in developing construction work packages for the electric distribution system using various software systems and construction standards. Distribution systems may be in an OH, UG, or URD environment. Project work may include joint use make ready, and street light projects. Work packages will be developed using Geographic Information Systems (GIS), Computer Aided Design (CAD) tools, Work Management Systems (WMS), and other client systems. Project work will require performing engineering calculations that may include: structural analysis of poles, guying, cable pulling, electric demand, transformer sizing, voltage drop and flicker, and coordination of protective devices. Assignments may also include: preparing forestry trimming requests, facilitating permit and Right-of-Way acquisition, development of a BOM, estimating costs, and customer advocacy such as acquiring easements. Work assignments will include travelling by motor vehicle to various project locations located throughout the area to conduct field investigations. The associate level candidate need not be proficient in applicate customer engineering, construction standards, and software systems. Training will be provided by Leidos. | 12/16/2024 |
| 1970 | Leidos Piscataway, NJ Associate Distribution Engineer Bachelors of Science in Engineering degree or Master’s degree (EE or CE preferred) Exp: 0+ years |
The successful candidate will have an interest in developing construction work packages for the electric distribution system using various software systems and construction standards. Distribution systems may be in an OH, UG, or URD environment. Project work may include joint use make ready, and street light projects. Work packages will be developed using Geographic Information Systems (GIS), Computer Aided Design (CAD) tools, Work Management Systems (WMS), and other client systems. Project work will require performing engineering calculations that may include: structural analysis of poles, guying, cable pulling, electric demand, transformer sizing, voltage drop and flicker, and coordination of protective devices. Assignments may also include: preparing forestry trimming requests, facilitating permit and Right-of-Way acquisition, development of a BOM, estimating costs, and customer advocacy such as acquiring easements. Work assignments will include travelling by motor vehicle to various project locations located throughout the area to conduct field investigations. The associate level candidate need not be proficient in applicate customer engineering, construction standards, and software systems. Training will be provided by Leidos. | 12/16/2024 |
| 1971 | Leidos Edison, NJ Associate Distribution Engineer Bachelors of Science in Engineering degree or Master’s degree (EE or CE preferred) Exp: 0+ years |
The successful candidate will have an interest in developing construction work packages for the electric distribution system using various software systems and construction standards. Distribution systems may be in an OH, UG, or URD environment. Project work may include joint use make ready, and street light projects. Work packages will be developed using Geographic Information Systems (GIS), Computer Aided Design (CAD) tools, Work Management Systems (WMS), and other client systems. Project work will require performing engineering calculations that may include: structural analysis of poles, guying, cable pulling, electric demand, transformer sizing, voltage drop and flicker, and coordination of protective devices. Assignments may also include: preparing forestry trimming requests, facilitating permit and Right-of-Way acquisition, development of a BOM, estimating costs, and customer advocacy such as acquiring easements. Work assignments will include travelling by motor vehicle to various project locations located throughout the area to conduct field investigations. The associate level candidate need not be proficient in applicate customer engineering, construction standards, and software systems. Training will be provided by Leidos. | 12/16/2024 |
| 1972 | Leidos Framingham, MA (Entry Level) Civil/Structural Engineer Bachelors of Science (BS) degree in Civil-Structural Engineering Exp: 0-2+ years |
We are seeking an Entry Level Civil/Structural Engineer with 0-2+ years of experience with a utility and/or utility consulting company doing design engineering. The candidate must have a strong educational background in design of steel structures, concrete structures, geotechnical engineering, and foundations. | 12/16/2024 |
| 1973 | Leidos Walled Lake, MI (Entry Level) Civil/Structural Engineer Bachelors of Science (BS) degree in Civil-Structural Engineering Exp: 0-2+ years |
We are seeking an Entry Level Civil/Structural Engineer with 0-2+ years of experience with a utility and/or utility consulting company doing design engineering. The candidate must have a strong educational background in design of steel structures, concrete structures, geotechnical engineering, and foundations. | 12/16/2024 |
| 1974 | Leidos Honolulu, HI Associate Distribution Engineer Bachelors of Science in Engineering degree or Master’s degree (EE or CE preferred) Exp: 0+ years |
Leidos is seeking an Associate Distribution Engineer in our Honolulu, HI office. The selected candidate will be required to work for a Leidos contractor for a period of 6 months with the possibility of converting to full-time direct Leidos employment. The successful candidate will have an interest in developing construction work packages for the electric distribution system using various software systems and construction standards. Distribution systems may be in an OH, UG, or URD environment. Project work may include grid hardening and reliability, substation optimization, joint use make ready and street light projects. Work packages will be developed using Geographic Information Systems (GIS), Computer Aided Design (CAD) tools, Work Management Systems (WMS), and other client systems. Project work will require performing engineering calculations that may include: structural analysis of poles, guying, cable pulling, electric demand, fault currents, and coordination of protective devices. Assignments may also include: preparing forestry trimming requests, facilitating permit and Right-of-Way acquisition, development of a BOM, estimating costs, and customer advocacy such as acquiring easements. | 12/16/2024 |
| 1975 | LFB USA Charlton, MA Manufacturing Technician II Bachelor’s Degree Exp: 1-3 years |
LFB USA has an immediate need in our Manufacturing group for a Manufacturing Technician. Level will be based upon experience. Responsible for the commercial production of drug intermediates (protein purification, buffer/equipment preparation), intended for further manufacture of drug products. This is a senior technician position in a regulated biomanufacturing setting. | 12/16/2024 |
| 1976 | LFB USA Charlton, MA Manufacturing Technician III Bachelor’s Degree Exp: 1-3 years |
LFB USA has an immediate need in our Manufacturing group for a Manufacturing Technician. Level will be based upon experience. Responsible for the commercial production of drug intermediates (protein purification, buffer/equipment preparation), intended for further manufacture of drug products. This is a senior technician position in a regulated biomanufacturing setting. | 12/16/2024 |
| 1977 | LGC Remote/Alexandria, MN Field Application Scientist I Bachelor's degree in Molecular Biology, Biochemistry, Chemistry, Genetics, or related field Exp: 1-3 years |
The Field Service Application Scientist I is a multi-disciplinary molecular biology and organic chemistry position that will contribute to the organization as part of our Global Field Service team, bringing curiosity, problem solving skills, and scientific acumen to LGC. The Field Service team supports various wings of the organization such as Laboratory Operations, Engineering, Sales, and Manufacturing. The scope of this position will include field-based customer support, customer assay verification/validation on LGC instrumentation, scientific support for applications development of our technologies, and providing various levels of technical support on our instrumentation and software. As part of this role, the Field Service Application Scientist I will have excellent customer-facing skills combined with a strong understanding of LGC products, including instrumentation and reagents. They will be required to operate laboratory equipment, on-site install of instrumentation, develop testing protocols, troubleshoot, analyse data, and keep current on emerging technologies in the fields of molecular biology, as well as organic chemistry. This position will be developed in a fusion of knowledge from genomics, PCR-based genetic analysis, laboratory automation, Oligo synthesis, DNA extraction, and customer support. | 12/16/2024 |
| 1978 | LGC Novato, CA GMP Manufacturing Technician I/II/III -KIT Lab Bachelor's degree in a related STEM field Exp: 1 year |
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management. This will be in our Kit Lab in Novato. Techs do final dry down (lyophilizatoin), column packing for purification, aliquoting and kitting of product. | 12/16/2024 |
| 1979 | LGC Novato, CA GMP Manufacturing Technician I/II/III - Synthesis Bachelor's degree in a related STEM field Exp: 1 year |
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management. This will be in our Synthesis department in our Novato Lab. | 12/16/2024 |
| 1980 | LGC Petaluma, CA Oligonucleotide Production Technician I - Purification Bachelor's degree in a related STEM field Exp: 0-2 years |
The Oligonucleotide Production Technician I - Purification will perform tasks associated with the purification of oligonucleotides in a high throughput, time sensitive manufacturing environment. Operates HPLC and/or RPC instruments. Comprehend chromatography techniques. Utilizes mass spectrometry and spectrophotometer instruments to obtain crude data. Schedule/Core Hours – Tues-Fri swing shift (1pm-11pm) schedule | 12/16/2024 |
| 1981 | LGC Clinical Diagnostics Milford, MA Manufacturing Associate Bachelor’s degree, with a concentration in Biology, Chemistry, or related science Exp: 1-3 years |
The Manufacturing Associate provides direct labor for the manufacturing of high-quality diagnostic products using manual and semi-automated equipment and prepares/completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 12/16/2024 |
| 1982 | LifeSensors Malvern, PA Cellular/Molecular Biologist BS/MS in biological sciences. Exp: 0-10 years |
LifeSensors, Inc. is a global leader in research involving the Ubiquitin Proteasome System (UPS) a cellular pathway that degrades damaged proteins. UPS provides a challenge as a new wave of drugs are emerging, such as PROtein TArgeting Chimeras (PROTACs) and Molecular Glues that target undruggable space. Our technologies are used worldwide by academic, pharma and biotech companies. As the company grows, it is critical that we continue to innovate. The scientist will be a part of research programs to develop innovative technologies, execute drug discovery projects for our clients, as well as drive the development of new products and product applications. They will write scientific articles, patents, and present data at national and international meetings. Please consult our website www.lifesensors.com for more details. | 12/16/2024 |
| 1983 | LivaNova Houston, TX Microbiology Technician Bachelor's Degree in Biology or related with completed coursework in Microbiology preferred Exp: No Exp |
This position is responsible for microbiological testing for the release of sterilization loads, for the periodical environmental monitoring of clean room areas and sterile barrier packing process of the devices. Successful candidate will work under general supervision to prepare all the microbiological media needed for in-house testing and as needed, to perform microbiological tests, environmental monitoring and packaging process tests which require standard procedures and instrumentation. | 12/16/2024 |
| 1984 | Alexion New Haven, CT Associate Scientist II, Injectable Drug Product Development MS degree, Biochemistry, Chemistry, Chemical Engineering or related discipline Exp: 1+ year |
The Associate scientist II will join Injectable Drug Product Development group to support the development of Alexion’s biotherapeutic candidates. This individual will design and execute experiments to develop injectable drug product formulations and process characterization studies, including analyzing samples and authoring technical reports. This individual will work in a dynamic team environment and routinely collaborate with other members of Injectable Drug Product Development as well as other groups in Product Development and Clinical Supply. | 12/16/2024 |
| 1985 | Lonza Portsmouth, NH QC Scientist I-Technical Transfer Bachelor's degree required; Advanced Graduate Degree (MS/PhD) preferred Exp: 0-4 years |
Lonza AG is thrilled to offer an outstanding opportunity for a Quality Control Scientist 1- Technical Transfer in our New Hampshire, USA location! This role plays a crucial role in our ambitious journey to uphold and improve our world-class standards in life sciences. As a member of our dedicated Quality Control team, you will directly contribute to technology transfer, validation, deviation support, routine testing, and investigation projects. This role is crafted for someone who excels in a collaborative environment and is dedicated to scientific excellence. | 12/16/2024 |
| 1986 | Lilly Lebanon, IN Sr./Principal Scientist - QC Bachelor’s degree (4-yr College) in a science field related to the lab (e.g., Chemistry, Biology, Microbiology, etc.) Exp: 1+ years |
The Senior/Principal Scientist - QC is part of the Lilly Lebanon API Quality Control team and provides technical leadership and expertise in the development, implementation, and maintenance of Quality Control laboratory systems to the Lilly Lebanon API site throughout the start-up, implementation, and day to day operations. The Senior/Principal - QC performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. The Scientist completes second person verification of other’s results. The Scientist also participates in laboratory root cause investigations, equipment evaluations and qualifications, and some quality system improvement initiatives by executing well-defined protocols and procedures. The Scientist shares technical information and best practice within plant sites or group. In addition, the Senior/Principal - QC will provide technical support to QC operations as part of the organization’s off-hours support strategy. After onboarding, this role will require a Short-Term Assignment (STA) of up to 6 months at a Lilly manufacturing site outside of the United States. | 12/16/2024 |
| 1987 | Lilly Lebanon, IN Manufacturing Scientist - Lebanon API Manufacturing Master's Degree in STEM Discipline (Chemistry preferred) Exp: 1 year |
The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 12/16/2024 |
| 1988 | Lilly Lebanon, IN Sr./Principal Scientist - QC Bachelor’s degree (4-yr College) in a science field related to the lab (e.g., Biology or Microbiology) Exp: 1+ year |
The Scientist-QC is part of the Lilly Lebanon API Quality Control team and provides technical leadership and expertise in the development, implementation, and maintenance of Quality Control laboratory systems to the Lilly Lebanon API site throughout the start-up, implementation, and day to day operations. The Scientist-QC performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. The Scientist completes second person verification of other’s results. The Scientist also participates in laboratory root cause investigations, equipment evaluations and qualifications, and some quality system improvement initiatives by executing well-defined protocols and procedures. The Scientist shares technical information and best practice within plant sites or group. In addition, the Scientist-QC will provide technical support to QC operations as part of the organization’s off-hours support strategy. | 12/16/2024 |
| 1989 | Lilly Lebanon, IN Sr./Principal Associate - QA Computer Systems Bachelor’s degree in Computer Science, Engineering, Life Sciences, or a technology-related field Exp: 1+ years |
The Associate - Computer Systems Quality Assurance is responsible for oversite of computer system validation at the Eli Lilly Lebanon API Manufacturing facility. This role includes working with Automation, QC labs, and Tech@Lilly persons to develop validation strategies for the approach to computer system validation in compliance with corporate standards; consultation and interpretation on applying and right-sizing validation requirements; maintaining corporate and site computer systems standards and practices; participating in internal and external Regulatory agency inspections; conducting evaluations of internal or supplier quality practices; maintenance of inspectional readiness; and external benchmarking of computer system validation practices. | 12/16/2024 |
| 1990 | Lilly Indianapolis, IN Scientist – API Manufacturing Process Support Master's Degree in STEM Discipline (Chemistry preferred) Exp: 1 year |
The Manufacturing Scientist provides the technical support required to achieve the reliable and compliant manufacture of the Active Pharmaceutical Ingredient External Manufacturing (API EM) portfolio which includes raw materials, intermediates, enzymes and bulk drug substances. The API EM Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and technically independent in setting up and executing a variety of experiments at the laboratory scale and conduct research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 12/16/2024 |
| 1991 | Lilly Indianapolis, IN Engineer, Drug Product Development Master’s or bachelor’s degree in engineering or in related fields Exp: 0-5 years |
We are seeking highly motivated professionals with experience in developing and commercializing parenteral drug product through various stages of clinical development. If you are interested in building platforms for new and novel therapeutic modalities and interested in building and leading a strong group of scientists exploring new frontiers into formulation and drug delivery strategies, you should consider joining our diverse team. | 12/16/2024 |
| 1992 | Lilly Indianapolis, IN Engineer - Facilities/Maintenance Bachelor of Science degree (Preferably in Chemical or Mechanical Engineering) Exp: 1 year |
This position is responsible for establishing and maintaining the reliable operation and qualified state of FUME owned equipment and business processes within the plant. Duties will require collaboration with the outsourced Facilities Management (FM) and Project Management (PM) service provider, Lilly Engineering Tech Center, and A/E firm to ensure facilities/systems meet the requirements of the business. | 12/16/2024 |
| 1993 | LSI Solutions Victor, NY Senior Molding Engineer Bachelor of Science Degree in a related discipline Exp: 1-5 years |
The Molding Engineer at LSI SOLUTIONS® plays a crucial role in creating and overseeing thermoplastic injection molding processes, utilizing scientific injection molding principles. The Molding Engineer will leverage their expertise to ensure consistent part quality and optimal cycle times. Additionally, they will provide oversight and foster collaboration with internal resources and external suppliers to ensure the implementation of best practices throughout the organization. | 12/16/2024 |
| 1994 | LSI Solutions Victor, NY Process Validation Engineer I Bachelor’s Degree in an engineering, technical or manufacturing discipline. Exp: 0-3 years |
The Process Validation Engineer will develop and execute validations to ensure regulatory compliance to established internal and external standards related to released product or current production. The individual will support the writing of validation protocols and reports, along with the gathering and analysis of data. | 12/16/2024 |
| 1995 | LSI Solutions Victor, NY Regulatory Associate Bachelor or Master’s degree in a technical, regulatory, or life sciences discipline Exp: 0-2 years |
The Regulatory Associate applies her/his experience, knowledge, organization skills, and communication skills in a wide variety of tasks. Regulatory Associates provide regulatory feedback and guidance based on medical device regulations and standards to the company throughout the development cycle. Regulatory Associates monitor regulations, standards, policies, and guidance for new and current compliance requirements that may have impact to the company. They maintain technical documentation and help to implement change control at LSI. Regulatory Associates are assigned to work in one or more of the following areas: Domestic, European, Rest of World, Labeling, and/or Clinical & Post Market Surveillance. Regulatory Associates assigned to Clinical projects contribute to clinical evaluation, investigator brochures, post-market clinical follow-up, and post market surveillance. All Regulatory Associates will also maintain full Quality and Regulatory compliance with all standards that govern the design, development, manufacturing, and distribution of our medical devices. | 12/16/2024 |
| 1996 | LSI Solutions Victor, NY Mechanical Engineer - Design I Bachelor’s Degree or higher in Engineering or related technical discipline Exp: 0-2 years |
As a Mechanical Engineer - Design, you will help bring a future generation of LSI products to market. You will be part of a team to further improve our current products that are already available by iterating on the innovative design. Working in a cross functional team, you will take ownership of all things related to the form, fit, function, and feel of the product. Other tasks include, stack up analysis, failure analysis, improvements for manufacturability, communicating design intent and inspection requirements with 3D and 2D CAD, and other tasks. | 12/16/2024 |
| 1997 | Lumanity Boston, MA Research Associate Master’s degree in health-related field Exp: 1-3 years |
We are seeking a Research Associate to join our Patient-Centered Outcomes team within our wider HEOR business. This is an excellent opportunity for an individual who is interested in conducting academic-type, patient-centric research. As our Research Associate, you will interact with patients with various diseases to determine how their diseases impact their health-related quality of life. Ultimately the research you do with help inform the development of clinical outcome assessments for use in clinical trials. | 12/16/2024 |
| 1998 | Lumen Seattle, WA Associate Scientist I MS/MSc degree in biochemistry, cell biology, immunology, virology, or related field of study Exp: 0-2 years |
Lumen is seeking a highly motivated, innovative Associate Scientist to join our team. The Associate Scientist will work with and support scientists in the Biologics research and development team. The work will involve various projects at different stages of the pipeline. The individual is expected to develop, optimize, design and execute a broad range of cell culture-based experiments and assays, as well as prepare and maintain cell line stocks. The individual is also expected to follow established protocols to perform assays, record, analyze, and report results. The position requires the ability to work as a team member in a fast-paced environment, have strong organizational skills, and take meticulous records. Effective communication skills are crucial in coordinating with the relevant teams to meet milestones and deadlines and in raising quality or troubleshooting issues as they may arise. The position will need to provide status updates and present in group meetings and company-wide meetings. | 12/16/2024 |
| 1999 | Magnet Biomedicine Boston, MA Sr. RA/Associate Scientist; Biophysics/Biochemistry MS in biophysics, biochemistry, chemical biology, or a closely related discipline Exp: 1+ years |
As a Sr. Research Assistant or Associate Scientist on the Screening, Biophysics, and Biochemistry team at Magnet Biomedicine, you will play a critical role in designing, executing, and interpreting biophysical and biochemical assays to discover and characterize small molecule chemical inducers of protein-protein interactions. This position offers a unique opportunity to contribute to the development of Magnet’s platform and the development of next-generation TrueGlue therapeutics. The successful candidate will collaborate with a team of passionate scientists to achieve our goal of bringing new medicines to patients. | 12/16/2024 |
| 2000 | Mallinckrodt Fenton, MO Quality Tech III Bachelors Degree in science related field (Chemistry, Biology) Exp: 1-3 years |
Provides technical support at an elevated level by developing solutions to routine problems of limited scope and complexity. Depending on the laboratory area, will perform analysis on Raw Materials, Intermediates, In-Process, Finished Product, or Stability samples using established analytical methods. | 12/16/2024 |
| 2001 | Mallinckrodt Raleigh, NC Operations Quality Engineer II B.S. degree in Engineering Exp: 1-5 years |
The role provides support for the various elements of the Quality System, including but not limited to the following: Deviations (Exceptions), Supplier Quality, Product complaints, Internal Audits, OOS, CAPA, Annual Product Review, Process control, Change Control, Validation, and identification/ recommendations for continuous improvement opportunities (internal/external). The Quality Engineer applies the appropriate statistical tools to analyze data, identify root cause and develop corrective actions for effective problem resolution of moderate to difficult scope and complexity. | 12/16/2024 |
| 2002 | Mallinckrodt St. Louis, MO Chemical Process Engineer B.S Degree in engineering or a technical related field (i.e. biology, chemistry, etc.) Exp: 1-3 years |
The Chemical Process Engineer is the recognized technical leader for manufacturing processes and for the improvement of existing processes. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies. Serve as main point of contact for manufacturing processes in their area in regard to safety, quality, and continuous improvement activities. | 12/16/2024 |
| 2003 | Mariana Oncology Watertown, MA Quality Control Analyst I/II Bachelor’s degree or Master’s degree in Biochemistry, Chemistry or related discipline Exp: 0-2 years |
We are seeking an experienced Quality Control Analyst I/II to join Mariana’s Analytical Quality Control function. You will be responsible for supporting the release and stability testing of our clinical therapies produced in our GMP manufacturing suite in Watertown. This person will play a role in creating and maintaining the highest standard of excellence for our therapies to treat cancer patients. | 12/16/2024 |
| 2004 | Mariana Oncology Watertown, MA Sr. Research Associate or Scientist, Biology MS in Biology, Cellular or Molecular Biology, Genetics, or a related discipline Exp: 1-2+ years |
We are seeking an experienced Senior Research Associate, Biology or Scientist, Biology to join Mariana’s Biology organization, advancing personalized medicine and radiopharmaceuticals. You will work as part of the team that is responsible for the validation of new targets and executing preclinical studies to advance the development of the next generation of radiotherapeutics. | 12/16/2024 |
| 2005 | Mariana Oncology Watertown, MA Research Associate, Discovery Chemistry B.S. or M.S. in Chemistry Exp: 0-2+ years |
We are seeking a highly motivated and energetic Research Associate, Discovery Peptide Chemistry to join Mariana’s Chemistry organization. The successful candidate will be a contributor to our targeted oncology platform in a pre-clinical, fast-paced discovery research environment through the purification and characterization of peptides. They will also work closely with the Medicinal Chemistry and Biology teams to support our drug discovery portfolio. The role requires the candidate to maintain broad scientific knowledge of high-performance liquid chromatography to execute peptide purification and characterization. The role also requires the candidate to become familiar with peptide synthesis and perform other chemistry tasks to support drug discovery efforts. The candidate should be a creative individual with good communication and interpersonal skills, and a willingness to step outside of their comfort zone. | 12/16/2024 |
| 2006 | Indivior Raleigh, NC Environmental Monitoring Technician Bachelor’s degree in Chemistry, Microbiology, Biology or other related Science Exp: 1-3 years |
The purpose of the EM Technician I is to perform routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 12/11/2024 |
| 2007 | Integer Brooklyn Park, MN Quality Engineer 1 Bachelor’s degree in a related field Exp: 0-3 years |
Adheres to Integer’s Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Performs work which involves conventional types of plans, investigations, surveys, structures, or equipment. Applies standard practices and techniques in specific situations, adjusts and correlates data. Recognizes discrepancies in results and follows operations through a series of related detailed steps or processes. Reviews test procedures and plans prior to implementation, conducts failure analysis and inspection on products, processes and materials. Investigates, develops and implements new process technologies of moderate scope. | 12/11/2024 |
| 2008 | Integra LifeSciences Plainsboro, NJ Manufacturing Engineer I Bachelor's degree in Engineering (Mechanical Engineering, Pharmaceutical Engineering, Chemical Engineering, Biomedical Engineering) Exp: 0-2 years |
The Manufacturing Engineer I will play a key role in the support of manufacturing operations, process scale–up, and manufacturing improvement activities. They will oversee projects to evaluate, analyze, and improve existing processes, support the development of new manufacturing processes, implement statistical process controls, analyze and trend existing process parameters, improve manufacturing yields, reduce scrap, and error proof manufacturing processes. | 12/11/2024 |
| 2009 | Integra LifeSciences Boston, MA Quality Engineer II - Design and Reliability Assurance (DRA) Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
The Quality Design and Reliability Assurance (DRA) Engineer II is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, specifically the Boston/ Braintree site. The role contributes and supports the design and development of new and improved products. The (DRA) Engineer II will interact with external design and development partners, participating on cross-functional project teams through all phases of the product development process, and assisting the technical team with planning, executing, documenting, and communicating testing activities. The role works with Product Development, Project Management, Regulatory, Marketing and Medical Affairs. | 12/11/2024 |
| 2010 | Integrated DNA Technologies (IDT) Coralville, IA Research Scientist II, Applied Science in Therapeutic Oligonucleotides Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field) Exp: 1+ years |
This position is part of the Applied Sciences for Therapeutic Oligonucleotides team in our Gene Writing and Editing Business Unit located in Coralville, Iowa and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things! Function as a scientist at the bench, under minimal supervision, reporting to a team or project lead and executing projects as part of IDT’s new Genomics Medicine Service offerings related to: off-target safety assessment for CRISPR-based editing systems, CRISPR guide RNA sequencing, and additional, custom projects associated with IDT’s Therapeutic Oligonucleotides business. Provide teamwide scientific support on all aspects of therapeutic oligonucleotides projects inclusive of lab work, project tracking and organization, data collection, data analysis, report generation, and data presentation. Plan and keep detailed experimental records in facilitating technology transfer of methods from R&D to the Gen Meds Services team; gain expertise in technologies to support further feasibility, development and validation of assays as well as propose ideas for broader use and application. Lend subject matter expertise to customer-specific oligo assessment of quality, performance, safety, etc. in cell-based, biochemical or analytical assays; assist in the definition of technical and experimental work plans related to on-going efforts to advance customer projects while supporting customer progress towards cGMP oligonucleotide synthesis. | 12/11/2024 |
| 2011 | Intelivation Tech Plymouth Meeting, PA Associate Product Development Engineer Bachelor’s Degree in Mechanical Engineering or Biomedical Engineering. Exp: 1+ years |
The Associate Product Development Engineer will be responsible for all engineering functions of their product lines. They will take products from concept through development and market introduction while following all aspects of Design Controls. The Engineer will be driven and self- motivated working towards on time market introductions. | 12/11/2024 |
| 2012 | Perceptive New Haven, CT Image Analyst I BS in a relevant field (e.g. engineering, physics, neuroscience, chemistry, or biology) Exp: 0-1 years |
The Image Analyst I performs analysis and quality control (QC) on imaging data and metadata. Image Analyst I personnel are responsible for quantitative results generated in an imaging study. Analysts will be trained on all assigned analysis pipelines. Following demonstration of proficiency, analysts will contribute toward QC and troubleshooting of complicated analysis cases. Image Analyst I staff are assigned to multiple projects where they will work under the supervision of the project’s lead analyst. Analysts may also be asked to contribute to other analysis-related duties (creation and editing of SOPs, ad-hoc efforts, etc.). | 12/11/2024 |
| 2013 | Medical Diagnostic Laboratories (MDL) Hamilton Township, NJ Lab Technician I Bachelor Degree in Biology, Chemistry, or related science field Exp: 9 months |
Medical Diagnostic Laboratories (MDL), a member of Genesis Biotechnology Group, is a CLIA certified clinical laboratory with multiple state licensing, specializing in state of the art, automated DNA based molecular analysis of a variety of chronic and infectious illnesses. MDL specializes and performs Polymerase Chain Reaction (PCR) with a larger menu of testing available in the field of infectious disease. Our main theme of research is in the field of Gynecology, Infectious Diseases, Infectious Arthritis, Tick-borne Diseases, Mycology, and Chronic Fatigue Syndrome (CFS). MDL is looking for a Laboratory Technician. The Laboratory Technician is responsible for printing labels and attaching requisitions to the corresponding specimens. | 12/11/2024 |
| 2014 | Iovance Biotherapeutics Philadelphia, PA Analytical Sciences & Technology Specialist II Bachelor’s degree in biology, Biochemistry, Microbiology, Chemistry, or related scientific field Exp: 1-3 years |
The Analytical Sciences & Technology Specialist II Specialist is accountable for the technical development of quality control methods and processes, method and instrument validations, and technical transfers related to Analytical and/or Microbiological quality control testing of products, raw materials, and packaging components at the site. This role is also responsible for operating and maintaining quality control instrumentation in compliance with cGMP/FDA regulations, Iovance standard operating procedures, and policies. Given the nature of the process, this role also necessitates expertise in quality control techniques, analytical instrumentation, sterility principles, and an understanding of radiation safety standards. | 12/11/2024 |
| 2015 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I, Microbiology Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1 year |
The Quality Control Analyst will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques. | 12/11/2024 |
| 2016 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I, Microbiology - Night Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-3 years |
The Quality Control Analyst I will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques. | 12/11/2024 |
| 2017 | Iovance Biotherapeutics Philadelphia, PA Quality Control Specialist I, Compliance Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-3 years |
lovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. lovance is seeking an Investigator I, for the Quality Control Compliance team who will in advance and close QC related investigations. Strong technical writing skills are required. Experience in a CAR-T or TIL environment is a plus. The ideal candidate will have experience working in a GMP-regulated laboratory with experience in writing investigations. | 12/11/2024 |
| 2018 | Iovance Biotherapeutics Philadelphia, PA Quality Control Specialist II, Compliance Investigator Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-5 years |
The Quality Control Specialist II, Compliance Investigator will assist the Laboratory Manager in advancing and closing QC related investigations. Strong technical writing skills are required with flow cytometry and ELISA experience. Experience in a CAR-T or TIL environment is a plus. The ideal candidate will have experience working in a GMP-regulated laboratory with knowledge of writing investigations but is not required. The position will be on-site at the Philadelphia location. | 12/11/2024 |
| 2019 | IQVIA Indianapolis, IN Laboratory Assistant BS in chemistry, biology, or medical laboratory technology Exp: 6 months |
We are seeking a Laboratory Assistant to join IQVIA Laboratories at Indianapolis, IN. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Laboratory Assistant is responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 12/11/2024 |
| 2020 | IQVIA Indianapolis, IN Scientist, LCMS Bachelor’s Degree in applied/laboratory sciences Exp: 0-2 years |
We are seeking a Scientist, LCMS to join IQVIA Laboratories at Indianapolis, IN. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The LCMS Scientist will be responsible for executing laboratory experiments accurately and contributing to the design of scientific procedures, supporting scientific discovery while adhering to Good Laboratory Practices (GLP). | 12/11/2024 |
| 2021 | IQVIA Ithaca, Ne Associate Scientist, Sample Preparation Bachelor’s Degree in a Life Sciences discipline required Exp: 6 months |
We are seeking a Associate Scientist, Sample Preparation to join IQVIA Laboratories at Ithaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Associate Scientist, Sample Preparation will be responsible for routine sample preparation duties, troubleshooting experiments, and preparing solutions and reagents to support laboratory operations. | 12/11/2024 |
| 2022 | IQVIA Indianapolis, IN Laboratory Associate BSc in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology Exp: 6 months |
We are seeking a Laboratory Associate to join IQVIA Laboratories at Indianapolis, IN. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Laboratory Associate, you will be responsible for performing routine analysis and laboratory testing procedures to ensure compliance with regulatory standards. | 12/11/2024 |
| 2023 | IQVIA Valencia, CA Lab Associate- Specialty Processing BS in chemistry, biology, or medical laboratory technology degree Exp: 6 months |
We are seeking a Laboratory Associate- Specialty Processing to join IQVIA laboratory business at Valencia, CA. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Laboratory Associate, you will be responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 12/11/2024 |
| 2024 | Johnson & Johnson Spring House, PA Associate Scientist, API Cell Therapy Process Development B.S. in Biological Sciences, Biomedical Engineering or Immunology Exp: 1-2 years |
We are looking for an energetic, highly motivated and collaborative Associate Scientist candidate with demonstrated expertise in cell therapy process development and process innovation. In this role, the successful candidate will be involved in process design, unit operation development, and parameter optimization studies resulting in the development of new production processes. The successful candidate will work as part of a cross-functional teams supporting pre-clinical and clinical programs, focused on autologous processes. | 12/11/2024 |
| 2025 | J-STAR Research Cranbury, NJ Research Scientist of Crystallization R&D MS or BS. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field with a focus on crystallization, solid-state chemistry, or m Exp: 1-5 years |
We are seeking a highly motivated and skilled Research Scientist to join our Crystallization R&D Department at Porton J-STAR. In this role, this position is responsible for leading group or contributing individually to conduct Solid Form Studies and pre-formulation will search for the right solid form and develop formulations to support preclinical and Phase I studies including PK, PD, efficacy, tox studies. This role is also responsible for Crystallization Process Development will develop crystallization processes to define and control final solid form of drug substances with desired solid-state attributes needed for optimum performance as well as drug intermediates for robust purification. The responsibilities of the position include, but are not necessarily limited to, the items listed below. | 12/11/2024 |
| 2026 | J-STAR Research Cranbury, NJ Research Scientist Master in Chemistry, Chemical Engineering, Pharmaceutical Chemistry, or Food Science required Exp: 1 year |
Pharmaceutical Ingredients (API), intermediates, impurities, starting material and excipients from drug substances and drug products. Analyze organic and inorganic compounds to determine chemical or physical properties, composition, structure, relationships, reactions, using chromatography, spectroscopy, spectrophotometry techniques including HPLC, UPLC, IC, GC, MS, UV,XRPD,DSC, TGA, NMR, and KF. Design and perform method verification and validation. Determine the specificity, linearity, accuracy, precision, forced degradation, robustness of the methods. Collect and analyze data, and maintain data integrity under GMP, GLP, and FDA regulations. Prepare documentation of test procedures and technical reports. Prepare, review, and/or approve methods, protocols, and development reports. Maintain laboratory instruments to ensure proper working order. Apply Scientific expertise to troubleshooting, laboratory investigation and problem resolution. Participate in maintaining high quality laboratory environment and comply with Health, Safety and Environmental responsibilities for the position. | 12/11/2024 |
| 2027 | J-STAR Research Cranbury, NJ Senior Research Scientist I/II, Analytical Development MS in Chemistry, Pharmaceutical Science or related field. Exp: 0-5 years |
J-STAR Research, Inc. operates as a contract research organization for pharmaceutical and biotechnology companies worldwide. It offers services in the areas of custom synthesis/contract research, process and analytical research, cGMP synthesis, crystallization process development, solid form screening and selection, pre/early formulation, and drug substance-drug product coprocessing. | 12/11/2024 |
| 2028 | J-STAR Research Cranbury, NJ Senior/Principal Scientist, Solid Form Selection/Preformulation Development MS in Chemistry, Pharmaceutical Science or related field. Exp: 0-5 years |
J-STAR Research, Inc. operates as a contract research organization for pharmaceutical and biotechnology companies worldwide. It offers services in the areas of custom synthesis/contract research, process and analytical research, cGMP synthesis, crystallization process development, solid form screening and selection, pre/early formulation, and drug substance-drug product coprocessing. | 12/11/2024 |
| 2029 | J-STAR Research Cranbury, NJ Analytical Research Scientist II/III (DPD) MS in Chemistry, Pharmaceutical Science or related field. Exp: 1-3 years |
The primary responsibility in this role is to perform analytical testing of drug substance, intermediates, drug product in support of J-Star’s drug product development projects. The incumbent should provide the expertise in characterization of drug product formulation using HPLC, GC, DSC, TGA, XRPD, dissolution apparatus, particle size analyzer, Karl Fischer titrator. Specifically, the incumbent will be responsible for analysis of formulations from preclinical through clinical formulation development, of oral solids, liquids, injectables and semi-solid dosage forms for new drug candidates. | 12/11/2024 |
| 2030 | J-STAR Research Cranbury, NJ Research Chemist MS degree in Chemistry, Chemical Engineering or related field Exp: 6 months |
Perform API crystallization process in compliance with cGMP and FDA regulations, utilizing analytical tools including chromatography, separation, and solvent selection; support crystallization process development by conducting studies involving compound properties and experimental conditions; participate in the scale-up development of enabling technology and experiments to facilitate the co-processing and development of API; conduct routine stability, performance, and evaluation studies for solid state characterization and pre-formulation support; support early drug crystallization process development for high potency compounds and controlled substance; purify pharmaceutical compounds using column chromatography, crystallization, trituration, extraction, and distillation; utilize experimental and simulation/modeling approaches to perform solvent selection and solve process challenges arisen from scale-up crystallization process; collect, analyze and maintain data integrity under Good Documentation Practice; write/review developmental chemistry, process optimization and process scale-up reports to support FDA requirements for CMC (Chemistry, Manufacturing and Control) sections of INDs/NDAs. | 12/11/2024 |
| 2031 | Jubilant Spokane, WA EM Specialist - Weekend Nights Bachelor degree with a major in Microbiology, Medical Technology or related science Exp: 1 year |
The Environmental Monitoring department performs the functions associated with sampling, initiating tests, collecting and evaluating test results related to defined quality parameters for surface, air, personnel, product and utility systems such as compressed gases and WFI. The Specialist oversees EM functions and personnel, schedules tasks and personnel, assists in training EM Technicians and gown training of all aseptic personnel. | 12/11/2024 |
| 2032 | Jubilant Spokane, WA QC Scientist I-III Bachelor of Science in Chemistry, Biology, or related hard science Exp: No exp |
The QC Scientist I/II/III performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw material, product disposition. In addition, this position demonstrates leadership, teamwork and technical expertise. | 12/11/2024 |
| 2033 | Jubilant Spokane, WA Validation Associate Bachelors of Science in technical or scientific discipline Exp: 1-2 years |
The Validation Associate works closely with the Validation Specialist in support of capital, contract, and compliance projects. This position is responsible for executing a variety of validation studies, including performance qualifications and/or requalifications for terminal and component sterilization work. | 12/11/2024 |
| 2034 | Jubilant Spokane, WA EM Specialist - Weekend Days Bachelor degree with a major in Microbiology, Medical Technology or related science Exp: 1 year |
The Environmental Monitoring department performs the functions associated with sampling, initiating tests, collecting and evaluating test results related to defined quality parameters for surface, air, personnel, product and utility systems such as compressed gases and WFI. The Specialist oversees EM functions and personnel, schedules tasks and personnel, assists in training EM Technicians and gown training of all aseptic personnel. | 12/11/2024 |
| 2035 | Jubilant Spokane, WA QC Microbiologist I-II Bachelor of Science in Microbiology or related hard science with microbiology emphasis Exp: No exp |
The QC Microbiologist I-II performs the microbial analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw materials/product disposition. | 12/11/2024 |
| 2036 | Katalyst South Plainfield, NJ Quality Analyst Master’s degree in pharmacy, biotechnology, chemistry, biochemistry, chemical engineering, mechanical engineering, industrial engineering, biomedical Exp: 6 months |
Involve in the design, development, implementation, testing, documentation & support of cGxP systems as per 21 CFR Part 11 & US FDA. Responsible for qualification & validation (IQ/OQ/PQ), master plans, protocols, changes requests, gap & root cause analysis, risk management plans, traceability matrix, summary reports for facilities, equipment, systems & processes. Preparation, review, authorize & submission of documentation for quality compliance & regulatory authorities. | 12/11/2024 |
| 2037 | KBI Boulder, CO Process Development Associate I B.S. degree in microbiology, biochemistry, chemistry, engineering, or related area Exp: 0+ years |
The Process Development Associate supports and executes laboratory studies within the KBI Process Development organization at KBI under general supervision. The Process Development Associate is able to execute lab work, with documentation and reporting that is consistent with Process Development compliance and Quality standards. The Process Development Associate is able to author basic operational documents for routine unit operations within the laboratory organization. The Process Development Associate is capable of executing lab studies from written documents and applies standard scientific approaches to solving technical problems. The Process Development Associate may serve as the point of contact for a specific laboratory project. The Process Development Associate works under the general supervision of laboratory management with work reviewed for soundness and accuracy. | 12/11/2024 |
| 2038 | KBI Durham, NC Manufacturing Associate I - Downstream (Night Shift) Bachelor’s degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment. | 12/11/2024 |
| 2039 | KBI Boulder, CO Process Engineer I Bachelor’s degree in Engineering, Biotechnology, Biochemical Engineering, or a related discipline. Exp: 0-2 years |
We are seeking a motivated Engineer I to join our engineering team and provide support for the manufacturing equipment at our biopharmaceutical manufacturing facility. In this entry-level position, you will assist with the maintenance, troubleshooting, and optimization of key manufacturing equipment, including UFDF (Ultra-Filtration/Diafiltration) systems, Centrifuges, Homogenizers, Fermenters, and other process equipment. You will work closely with experienced engineers and cross-functional teams to ensure the efficient and compliant operation of the manufacturing systems, while adhering to cGMP (current Good Manufacturing Practices) and regulatory standards. | 12/11/2024 |
| 2040 | KBI Durham, NC Microbiology Associate II Master’s degree in Microbiology, Biology or related technological field of science. Exp: 1-3 years |
The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. | 12/11/2024 |
| 2041 | KBI Boulder, CO Research Analyst I B.A. or B.S. degree in chemistry, biochemistry or related are Exp: 0-2 years |
Analyst position in a growing team that supports a variety of testing in support of the manufacturing of biopharmaceutical products in a contract development and manufacturing space. | 12/11/2024 |
| 2042 | KBI Boulder, CO Research Associate I B.A. or B.S. degree in chemistry, biochemistry or related area Exp: 0-2 years |
Analyst position in a growing team that supports a variety of testing in support of the manufacturing of biopharmaceutical products in a contract development and manufacturing space. | 12/11/2024 |
| 2043 | KBI Durham, NC Validation Engineer l Bachelor’s degree in Chemical Engineering, Industrial Engineering, Biomolecular Engineering, Mechanical Engineering, or related scientific field. Exp: 1-3 years |
The Validation Engineer I/II will be responsible for facilitating the validation lifecycle process for the Validation Department to ensure all equipment and systems are in a qualified state suitable for the intended use. This may entail, assisting with the planning, development, project management, and execution of life cycle engineering and validation lifecycle documentation elements of engineering and validation lifecycle design, commissioning, maintenance, qualification, and the interfaces with quality system lifecycle compliance requirements. | 12/11/2024 |
| 2044 | Krystal Biotech Pittsburgh, PA Process Validation Associate Bachelors’ Degree in Chemical Engineering, Biomedical Engineering, or related Exp: 1+ year |
Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site. | 12/11/2024 |
| 2045 | Krystal Biotech Moon Township, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 12/11/2024 |
| 2046 | Gilson Middleton, WI Electrical Engineer I Bachelor of Science degree in electrical engineering or a related science Exp: 1 year |
Responsible for the design and analysis of hardware and firmware integration for new products and modifications to existing products. Additional responsibilities may include some project management and the ability to work on cross-functional product development teams. Basic research may be done during early project feasibility studies or for new concept investigations. Assignments will be broad in nature, requiring initiative, originality, and ingenuity. | 12/05/2024 |
| 2047 | Globus Medical West Carrollton, OH Associate Engineer, Manufacturing Bachelor’s degree in an engineering discipline preferred Exp: No exp |
As an Assoicate Manufacturing Engineer, you will develop, implement and maintain methods, operation sequence, and processes in the manufacturing of parts, components, sub-assemblies, and final assemblies. Support new initiatives and productivity targets for given manufacturing processes. Responsibilities will also include participation in design reviews, design transfer to production as it relates to the development of manufacturing processes, post-processing development, equipment and process validations, process definition for machine operation and maintenance requirements, test/inspection methods, fixturing, gauging and applying inspection and process control techniques. | 12/05/2024 |
| 2048 | Glyphic Biotechnologies Berkeley, CA Scientist, Assay Development BS/MS in molecular biology, biochemistry, chemistry or related fields Exp: BS/MS with 2+/1+ (for Scientist I) |
We are seeking an experienced Assay Development scientist to conduct experiments that will enable the next generation of sensitive, accurate, and scalable single-molecule protein sequencing. The ideal candidate will thrive in a dynamic research team as part of an intellectually stimulating and collaborative project. As a scientist at our early-stage startup, the candidate will have an opportunity to apply their creativity, knowledge, and enthusiasm and make significant contributions to an exciting and impactful project. The scientist will report to Director of Assay Development and bring their expertise in molecular biology to a cross-functional project at the interface of molecular biology, chemistry, bioinformatics, and automation. This is a full-time, exempt, in-person role based in Berkeley, CA. | 12/05/2024 |
| 2049 | Gore Associates Flagstaff, AZ Industrial Engineer Bachelor’s degree in Industrial Engineering or degree in related disciplines Exp: 1 year |
We are looking for Industrial Engineers to join our manufacturing teams for multiple openings. You will be a member of a cross-functional team supporting commercialized medical device manufacturing. The industrial engineer’s responsibility will be to apply industrial engineering fundamentals and contribute to Lean process improvements, data analysis, cleanroom layout design, and demand and capacity plans. The ideal candidate will be passionate about providing Industrial Engineering support for state-of-the-art implantable medical devices, energized by working for a world-class manufacturer and collaborating on cross-functional teams, recognize the importance of building and maintaining strong interpersonal relationships and possess strong attention to detail, and excellent documentation skills. This position will be located at our facility in Flagstaff, Arizona, with the possibility of a hybrid remote work arrangement, depending upon the responsibilities of the role and business needs. | 12/05/2024 |
| 2050 | Grifols Vista, CA Manufacturing Technician I Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 12/05/2024 |
| 2051 | Grifols San Francisco, CA Senior Research Associate Masters degree in Life Sciences or related discipline Exp: 1 year |
We are seeking a talented and highly motivated Senior Research Associate to support our diverse antibody therapeutics pipeline. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 12/05/2024 |
| 2052 | Grifols San Diego, CA Research Associate 2 Molecular R&D B.A./B.S./M.S. Molecular Biology, Chemistry, Biochemistry or related field. Exp: 1-3 years |
Research Associate 2 is responsible for designing and performing experiments while collaborating and communicating effectively. | 12/05/2024 |
| 2053 | Grifols Research Triangle Park, NC Senior Associate Research Scientist I Masters in Biology, Biochemistry, Chemistry, or Toxicology Exp: 1 year |
This Senior Associate Research Scientist I position is in the CMC Development, Bioanalytics, Analytical Operations Group. The selected candidate will be responsible for conducting testing of process intermediates and final container in support of manufacturing, process development, developmental stability, validation and other R&D projects. Other responsibilities include cGXP documentation, sample login, data review, instrument maintenance and troubleshooting, data analysis, and other tasks assigned by management. The analyst may participate in development, execution, and qualification of new analytical test methods for characterization. The incumbent will be expected to work effectively under minimal supervision, and contribute to the team effort to support R&D projects. | 12/05/2024 |
| 2054 | Grifols Clayton, NC Assistant Biologist BS degree in biology, chemistry, or related field Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in SFF and PFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. | 12/05/2024 |
| 2055 | Grifols Clayton, NC Automation Engineer I/II Master’s Degree - Engineering, Automation, Computer, Industrial, Manufacturing, Related Exp: 0-1 years |
The Automation Engineer I is an entry level professional who is responsible for using technology to improve and streamline a manufacturing process through automation. Depending on their specific assignment, this person provides automation support for projects or within a specific area, or provide validation support for automation projects. The Automation Engineer I can also integrate into a project team. The incumbent is knowledgeable in Automation with the capability to learn specific control systems, instrumentation, process, utilities, or qualification testing. He/she supports meeting customer needs and business goals. In addition, he/she will collaborate with other automation engineers. The Automation Engineer II is a junior level professional who is responsible for using technology to improve and streamline a manufacturing process through automation. Depending on their specific assignment, this person provides automation support for projects or within a specific area or provide validation support for automation projects. The Automation Engineer II will also integrate into supporting a large-scale project. He/she is recognized as proficient in their field such as specific control systems, instrumentation, process, utilities, or qualification testing. He/she meets customer needs in support of business goals. In addition, the incumbent will collaborate with other automation engineers. | 12/05/2024 |
| 2056 | Grifols Norfolk, VA Field Service Engineer Bachelor’s degree in Engineering, Technical or related Scientific Discipline Exp: 0-2 years |
The position will be responsible for customer relationship management and collaborating with interdepartmental teams to ensure proper resolution and close out of regulated documentation in the CRM system. The FSE will manage all preventative maintenance and system upgrades of instrumentation and its interface at the customer site and provide troubleshooting to diagnose and resolve technical issues on a variety of electromechanical, fluidic and medical devices . Deals with diverse and oftentimes complex issues where analysis may require in-depth evaluation of many factors, and functions as the reference for troubleshooting, investigations and log analysis for FSE team members within and outside the assigned region. The team is looking for an individual with first electrical / mechanical work experience. Independently exercises judgement in evaluating methods and determine criteria for obtaining solutions is a must. The FSE is required to live within 50mi of the Metro Atlanta area. | 12/05/2024 |
| 2057 | GSK Collegeville, PA Associate Scientist/Engineer – Sterile Process Engineering BS degree in Pharmaceutics, Biology, Biochemistry, Chemistry, Chemical Engineering, or related scientific discipline Exp: 1+ year |
Are you looking for a collaborative Associate Scientist role that allows you to contribute to designing innovative ways to use Engineering, Process Analytics Technologies, Automation and Modelling to develop medicines for patients? If so, this opportunity within the Sterile Process Engineering team would be the right fit for you. As an Associate Scientist you will join the Sterile Process Engineering and Analytics department of the Drug Product Development organization within the GSK R&D. You will primarily support drug product manufacturing process development using the small-scale capabilities, platform initiatives, combination product development, technology transfers, and new technology implementation for products in the pipeline. | 12/05/2024 |
| 2058 | Guardant Health Redwood City, CA Scientist I - Technology Development Bachelors or Masters Degree in Molecular Biology, Genetics, Biochemistry, or related field. Exp: 0-3 years |
The Technology Development Department is responsible for developing, validating, and implementing the tests used by Guardant Health for cancer detection. This role will be within the Product Development wing of Technology Development. The Product Development group is primarily responsible for late-stage assay development, including interfacing with early-stage assay development to finalize the assay, verifying and validating the product, and supporting transfer of the product to the Guardant health clinical laboratory and subsequent launch. The current focus of the role will be supporting regulatory submissions to both FDA and ex-US regulatory agencies as subject matter experts in analytical and clinical validation studies. However, the full scope additionally includes LDT and RUO product development and validation utilizing standard design control processes. | 12/05/2024 |
| 2059 | Guardant Health Redwood City, CA Biospecimen Associate I Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field Exp: 1-2 years |
The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow. In addition to the primary role of biospecimen management, there may be a need to provide back-up support (non-testing) to the Analytical and/or Post-Analytical team. It is imperative that the Biospecimen Associate has demonstrated the ability to work independently, but also functions effectively as a member of the Guardant Health team. The nature of the work requires keeping organized records, excellent attention to detail, effective written and verbal communication skills, the ability to multi-task and be flexible with tasks and schedules, and the ability to work independently in a team environment. | 12/05/2024 |
| 2060 | FL106 (Flagship Pioneering) Cambridge, MA (Senior) Research Associate, Chemistry Bachelor’s degree in chemistry or a related field (e.g. organic chemistry, biochemistry, biotechnology or pharmaceutical science) Exp: 1+ years |
FL106 is seeking a highly motivated (Senior) Research Associate with expertise in chemistry to play a vital role in the company’s efforts to develop and validate novel target discovery approaches. The candidate must be independent, goal oriented, have excellent communication skills and be willing to work in a highly dynamic and fast-paced entrepreneurial environment. This is a unique opportunity to drive the growth of an early-stage biotechnology company where you can contribute to the next frontier of genetic medicines. We are looking for collaborative, enthusiastic problem-solvers to join our team, driven by a shared goal of making a practical impact. | 12/05/2024 |
| 2061 | FL106 (Flagship Pioneering) Cambridge, MA Senior) Research Associate, In Vitro, Cell and Molecular Biology Bachelor’s degree in Biology or a related field Exp: 1+ years |
FL106 is seeking a highly motivated (Senior) Research Associate with expertise in Cell and Molecular Biology to play a vital role in the company’s efforts to validate novel target discovery approaches. The candidate must be independent, goal oriented, have excellent communication skills and be willing to work in a highly dynamic and fast-paced entrepreneurial environment. This is a unique opportunity to drive the growth of an early-stage biotechnology company where you can contribute to the next frontier of genetic medicines. We are looking for collaborative, enthusiastic problem-solvers to join our team, driven by a shared goal of making a practical impact. | 12/05/2024 |
| 2062 | Heraeus Dayton, OH Quality Engineer Bachelors Degree in Chemistry or related field Exp: 1-2 years |
Facilitates the investigation and response to customer complaints and internal issues. Determine and eliminates root causes and diminish defect occurrences or quality incidents in the process. Supports the Quality Manager with internal and external audits, customer surveys, and respond or resolve corrective and/or preventive actions and verifications. Develops new approaches to solve problems identified during quality assurance activities. Supports the Quality Assurance group in streamlining Quality documentation. Communicates significant issues or developments identified during quality assurance activities and provides recommended process improvements to management. Documents data obtained during all quality assurance activities, consistent with company policies and procedures. Perform capability studies and statistical analysis using methods such as FMEA, GR&R, SPC, and SQC. Organize data from various sources into Excel for statistical analysis. Applies statistical analysis to investigate historical trends. Perform control charting and review prior to product shipment. Participate in pFMEA, Cpk, control plan; file and maintain related records. | 12/05/2024 |
| 2063 | Hesperos Orlando, FL Engineer Associate I Bachelor’s degree Exp: 1 year |
You are experienced in software development for scientific data and scientific equipment, and developing algorithms, software, and interfaces. You are conscientious and pay almost obsessive attention to detail, as organized documentation is second nature. You are curious, love learning, and are eager to take on hard problems. You thrive in a fast-paced environment and enjoy pushing the edge of what is possible. You are resourceful and like to work independently but are not shy to ask for advice. You are a cross-disciplinary team member, who is excited to work with and learn from other engineers, biologists, chemists, modelers, and experimentalists. You are comfortable communicating across teams. You deliver. You know that what matters is delivering a solution that works every time. | 12/05/2024 |
| 2064 | Biogen Research Triangle Park, NC Manufacturing Associate - Biologics Bachelor’s Degree (STEM preferred) Exp: Recent Grad/Entry Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 12/05/2024 |
| 2065 | Biogen Research Triangle Park, NC Manufacturing Associate IV Bachelor’s Degree (STEM preferred) Exp: 6 months |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling operations, and our teams operate across the following units: Component Preparation, Compounding, Parenteral Filling/Lyophilization, Visual Inspection | 12/05/2024 |
| 2066 | Biogen Cambridge, MA Sr. Associate Scientist, DMPK In-Vivo MS degree in Pharmaceutical Sciences, Biochemistry, Chemistry, or a related field Exp: 0-2 years |
Biogen is seeking a highly motivated scientist to join the Drug Metabolism and Pharmacokinetics (DMPK) department at our Kendall Square site in Cambridge, Massachusetts. The role requires hands-on experience in conducting in-vivo studies in rodents, and basic familiarity with the concepts of pharmacokinetics (PK). The ideal candidate will not only conduct PK studies in nonclinical models but will also conduct animal surgeries when necessary. | 12/05/2024 |
| 2067 | HighRes Biosolutions Beverly, MA Mechanical Engineer/Document Control Specialist Bachelors degree in a relevant field of study Exp: Entry Level |
As a Document Control Specialist and Entry Level Mechanical Engineer at HighRes Biosolutions, you will work closely with engineering and operations to create, maintain, and check CAD and manufacturing documentation required to fabricate, build, and qualify our products. In addition, you will be a member of the mechanical engineering team, assisting in the design, development, testing, and maintenance of the HighRes hardware product catalog. The qualified candidate will have experience using SolidWorks and standard engineering drafting practices to document product designs. 50 – 60% of your time will be spent focused on document control with the remainder contributing to the work output by the mechanical engineering team. HighRes Biosolutions is a leader in the field of lab automation. Our mission is to improve human health through life science robotics, and we accomplish that through innovative software and hardware developed by a passionate team. Our systems and devices are used by the top pharmaceutical, biotech, and academic research labs throughout the world to help discover new drugs faster and more efficiently. In this role you will have a direct hand in helping deliver these lab automation solutions. | 12/05/2024 |
| 2068 | Hologic Newark, DE Supplier Quality Engineer Bachelor’s degree (BA or BS) from a university in Electronics or Mechanical Engineering or related Engineering field Exp: No exp |
Are you a detail-oriented and passionate engineer ready to kick-start your career in supplier quality? We are seeking a dynamic Supplier Quality Engineer to join our innovative team onsite in Newark, DE, supporting our Breast and Skeletal Health Division. This is an exciting opportunity to work closely with suppliers, ensure the highest quality standards, and make a significant impact on women's health. | 12/05/2024 |
| 2069 | Hologic San Diego, CA Systems Engineer 1 Bachelor's degree in Engineering (Mechanical, Electrical, Biomedical, or related field) or a Master's degree in a relevant field Exp: 6+ months |
We are seeking a motivated and detail-oriented Systems/Bioengineer to join our team. This role will involve working on the integration and automation of sample collection, nucleic acid extraction, and amplification processes for our innovative instrument platforms. The successful individual will be familiar with fixturing mechanical subcomponents and building breadboard systems. The instrument/subcomponents will utilize disposable parts. Therefore, the position requires basic knowledge in consumable molding, plastic sealing/welding, and amplification technologies such as PCR. | 12/05/2024 |
| 2070 | Hologic Marlborough, MA Manufacturing Engineer 1 Bachelors degree in Engineering or Science. Exp: 0-2 years |
Responsible for supporting medical device manufacturing engineering projects, processes, test and activities for Hologic’s product lines. Works with the manufacturing team and supports management goals for manufacturing activity aimed at providing cost efficient operations. To maintain engineering responsibility for the manufacture and performance of assigned product line(s). Participate in the transfer of design changes from design engineering to manufacturing. Performs root cause analysis and recommends corrective actions in response to manufacturing issues. Facilitate the transfer of major design changes that affect the product line. Communicate changes to manufacturing personnel. Assure that unique training requirements are met. Continuously support work to improve manufacturing methods, efficiency and product quality. Support the specification to provide the necessary tools, equipment, and fixtures for the assigned product line. | 12/05/2024 |
| 2071 | Hologic San Diego, CA Research Associate 1, Oncology B.A./B.S./M.S. in Biology, Biochemistry, Molecular Biology or related field Exp: B.A./B.S.: 1-2 years; M.S.: 0-1 years |
Biotheranostics, Inc., a Hologic company, is looking for an experienced research associate to join our oncology research and development team to strengthen our efforts in oncology diagnostic product development and research. Biotheranostics is a leader in the development of evidence-based biomarkers to address unmet medical needs and is experiencing dynamic and rapid growth. Its leading products are the Breast Cancer Index® (BCI) and CancerTYPE ID® (CTID). The company is based in San Diego, CA and offers testing services through its CLIA-certified, CAP-accredited laboratory. | 12/05/2024 |
| 2072 | ICON San Antonio, TX Laboratory Sample Processor (PRN) Bachelor’s degree Exp: 1 year |
We are currently seeking a Laboratory Assistant to join our diverse and dynamic team at ICON at our San Antonio TX site in a PRN (as needed) capacity. The Laboratory Assistant aids the technical staff with the handling and storing of and accounting for biological lab specimens, quality control and any other relevant tasks. | 12/05/2024 |
| 2073 | ICON Lenexa, KS Laboratory Assistant Bachelor’s degree Exp: 1 year |
If you have experience handling biological lab specimens and prepping samples for delivery to a clinical laboratory; learn how you can play a key role as Laboratory Assistant for ICON Laboratory Services which is dedicated exclusively to central laboratory testing and the associate services for clinical trials. | 12/05/2024 |
| 2074 | ICON Portland, OR Medical Technician I BSc or BA: Biology, Molecular Biology or Chemistry Exp: 1+ year |
This is an exciting opportunity to work within a fast-paced CLIA and CAP certified laboratory for a leading global provider of outsourced services to the pharmaceutical, biotechnology and medical device industries. Our Medical Technicians ensure the highest quality nucleic acid extractions, ensure timely storage of clinical samples, and perform general duties for the molecular laboratory, as directed. | 12/05/2024 |
| 2075 | Imperative Care Campbell, CA Manufacturing Engineer I Bachelor’s degree in engineering or related disciplin Exp: 0-2 years |
As a new professional in this field, this position will use acquired professional education and/or experience in mechanical, electrical, and/or pneumatic systems to focus on supporting activities related to the equipment used for manufacturing our company products. An individual in this role will be involved in drafting equipment installation/operation qualifications. This role will participate in the analysis of design studies to determine equipment capabilities, programs and solutions for increasing uptime that affect manufacturing processes. This hands-on engineering position will resolve issues related to calibration, preventive maintenance, and equipment repairs in accordance with maintenance schedules, manufacturer specifications, technical notices, equipment upgrades and safety issues. This position will address equipment related nonconformances and lead corrective and preventive actions. | 12/05/2024 |
| 2076 | INCOG BioPharma Fishers, IN Manufacturing Specialist BS in biological sciences/biotechnology Exp: 1 year |
INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation. The Manufacturing Specialist is a key technical role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, or within highly regulated industries. The Manufacturing Specialist’s primary responsibility is to efficiently and safely setup and operate various pieces of production equipment within the facility. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should possess a strong mechanical aptitude with strong trouble shooting skills on manufacturing equipment. They should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and inspire problem solving & solution driven thinking. | 12/05/2024 |
| 2077 | INCOG BioPharma Fishers, IN Formulation Specialist BS in biological sciences/ biotechnology Exp: 1+ year |
The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 12/05/2024 |
| 2078 | INCOG BioPharma Fishers, IN MSAT Engineer Bachelor's degree in science or engineering Exp: 0-3 years |
The Manufacturing Science and Technology Engineer will be responsible for supporting all facets of tech transfer, process validation, GMP floor support, and continued process verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the business to ensure robust and reliable production processes are established. The MSAT Engineer is responsible for scaling up and transferring processes into full scale manufacturing process based on data generated internally or received from the client. | 12/05/2024 |
| 2079 | INCOG BioPharma Fishers, IN MSAT Engineer (2nd Shift) Bachelor’s or Master’s degree in science or engineering Exp: 0-2 years |
The Manufacturing Science and Technology Engineer will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the business to ensure robust and reliable production processes are established. The MSAT Engineer is responsible for scaling up and transferring processes into full scale manufacturing process based on data generated internally or received from the client. | 12/05/2024 |
| 2080 | INCOG BioPharma Fishers, IN Manufacturing Specialist- Formulation BS in biological sciences/ biotechnology Exp: 1+ year |
The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 12/05/2024 |
| 2081 | Incyte Wilmington, DE Research Scientist / Sr. Research Scientist, Cell Line Development Master’s degree in molecular or cell biology, chemical engineering, or related field. Exp: 1-3 years |
The Research Scientist/Senior Research Scientist in Cell Line Development will be responsible for the development of commercially viable cell lines that will be used in the production of therapeutic recombinant proteins such as fusion protein, monoclonal and bispecific antibodies. | 12/05/2024 |
| 2082 | Indee Labs Berkeley, CA MEMS Engineer Masters Exp: 1-3 years |
We are seeking an MEMS Engineer or Senior MEMS Engineer to join the team full time to accelerate the development of Hydropore in our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 12/05/2024 |
| 2083 | Indee Labs Berkeley, CA Scientist, Immunology Masters Exp: 1-3 years |
We are seeking a Scientist or Senior Scientist, Immunology to join the team full time to accelerate the biological development of Hydropore at our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 12/05/2024 |
| 2084 | Indee Labs Berkeley, CA Senior Bioengineer Masters Exp: 1-3 years |
We are seeking a Bioengineer or Senior Bioengineer, Immunology to join the team full time to accelerate the biological development of Hydropore at our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 12/05/2024 |
| 2085 | Indica Labs Albuquerque, NM Integration Solutions Engineer Bachelor’s degree in computer science (CS), Computer Engineering (CE), Electrical Engineering (EE), Math or related. Exp: 1 year |
Indica Labs is looking for an experienced Integration Solutions Engineer. You will be responsible for configuring, optimizing, and maintaining integrations between various software systems and platforms, as well as managing integration projects and assisting with software installation and setup at client sites. | 12/05/2024 |
| 2086 | Evotec Seattle, WA Senior Associate Scientist Masters in biochemistry, chemistry, biophysics, chemical engineering, or related fields Exp: 0-1 years |
Just-Evotec Biologics is seeking an energetic, team-oriented scientist for a hands-on, laboratory based role supporting early and late stage drug product development including molecular assessment and formulation stability studies of antibodies, Fc-conjugates and other novel protein based molecules. The position requires experience with protein formulation development including stability study design and execution, data interpretation and cross functional team communication. The candidate should also have experience with analytical laboratory skills including chromatographic, electrophoretic, and spectroscopic techniques. The candidate must possess a strong ability to work as a team member while supporting multiple projects. Strong organizational, written, and verbal communication skills are necessary. The ideal candidate is efficient, curious, creative, enthusiastic, works well independently and in teams, and looks for ways to improve processes and technology. | 11/27/2024 |
| 2087 | Exactech Gainesville, FL Manufacturing Engineer Bachelor's degree Exp: 1-3 years |
Create and maintain the lowest cost, highest quality machining & manufacturing processes, tooling and supporting documentation for all parts produced. | 11/27/2024 |
| 2088 | Exelixis Alameda, CA QA Associate - Core Bachelor’s degree preferably in the life sciences or STEM disciplines Exp: 1-3 years |
The QA Core Associate supports QA Partner in GxP supplier quality management activities, vendor qualification, audit preparation, audit closure, audit observation tracking, vendor retirement, metrics collection, and records management. The position ensures data inputs in the Veeva supplier quality and audit modules and ensure audit logistics in regulatory and partner inspections. | 11/27/2024 |
| 2089 | Exelixis Alameda, CA Scientist II, Drug Substance Manufacturing BS/BA degree in chemistry, chemical engineering, life sciences or related discipline Exp: 1 year |
Responsible for the comprehensive review of documents and data analysis related to executed batch record packages, master batch records, protocols, reports, deviations, change controls, specifications, and risk assessments generated within the Commercial Drug Substance Manufacturing Group and related Contract Manufacturing Organizations (CMOs) to ensure compliance with all established and approved procedures. | 11/27/2024 |
| 2090 | Exelixis Alameda, CA Scientist II (Tumor Biology) MS/MA degree in related discipline Exp: 1 year |
The successful and highly motivated candidate will evaluate the activity of small molecule inhibitors in cell-based assays for oncology drug discovery. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will actively contribute to develop cell-based functional assays and problem resolving, reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet deadlines. | 11/27/2024 |
| 2091 | Bio-Techne San Marcos, CA Chemistry Associate Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 years |
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 11/27/2024 |
| 2092 | Eyepoint Pharmaceuticals Watertown, MA Research Associate Bachelor degree in pharmaceutics or pharmaceutical sciences Exp: 1-3 years |
Eyepoint Pharmaceuticals is seeking a talented formulator to join our Development group in Watertown MA. Our department works closely with Operations and Regulatory affairs department to formulate and manufacture innovative ocular formulations. Ideal candidate should have a strong background in advanced physical chemistry, the use of polymers in Ocular Delivery. The selected scientist will design and conduct experiments to develop ocular formulations as well as to design and conduct robust analytical experiments for the designed formulations. The qualified candidate will interact with other departments, CMOs, participate in cross functional teams, contribute to the product development plans, and authorship of publications and pertinent sections of regulatory submissions, as needed. Additionally, the candidate must be a strong team player with excellent communication skills working in a complex cross-functional environment. The candidate must be able to work independently and take initiative by providing input on multiple projects. The candidate must be able to think critically, intellectually curious, and show resilience and courage to resolve complex formulation and manufacturing problems. | 11/27/2024 |
| 2093 | Eyepoint Pharmaceuticals Watertown, MA Process Engineer I Bachelor of Science, Engineering Exp: 1-2 years |
EyePoint is seeking a motivated Process Engineer I with excellent interpersonal skills to join our team. This person will be responsible for process sustaining and improvement of all components, device and packaging related projects. This position requires the application of continuous improvement, equipment oversight, trending, layout plans, testing, data analysis and report writing to resolve and improve manufacturing efficiencies. Candidate must be able to effectively collaborate with internal R&D, Quality, Regulatory and Operations departments and with external vendors and suppliers to deliver against project timelines and maintain process sustaining activities. The ideal candidate possesses the ability to develop credibility and trust as a technical resource to contribute to the company’s growth, productivity, and innovation. | 11/27/2024 |
| 2094 | Eyepoint Pharmaceuticals Watertown, MA Process Engineer I Bachelor of Science, Engineering Exp: 1-2 years |
EyePoint is seeking a motivated Process Engineer I with excellent interpersonal skills to join our team. This person will be responsible for process sustaining and improvement of all components, device and packaging related projects. This position requires the application of continuous improvement, equipment oversight, trending, layout plans, testing, data analysis and report writing to resolve and improve manufacturing efficiencies. Candidate must be able to effectively collaborate with internal R&D, Quality, Regulatory and Operations departments and with external vendors and suppliers to deliver against project timelines and maintain process sustaining activities. The ideal candidate possesses the ability to develop credibility and trust as a technical resource to contribute to the company’s growth, productivity, and innovation. | 11/27/2024 |
| 2095 | Flare Therapeutics Cambridge, MA Research Associate, Compound Management Bachelor’s degree in a relevant scientific discipline Exp: 0-3 years |
In this role you will Be responsible for managing Flare’s internal and external compound inventory using Mosaic SampleBank inventory system. Process and incorporate all new compounds into inventory using various liquid handlers. Collaborate with Medicinal Chemistry/Biochemistry/Biology/Proteomics/Translational Biology team members to provide support for fulfillment of dry/liquid compound requests and prepare custom assay ready plates. Utilize and troubleshoot various lab instrumentation such as Echo Acoustic Liquid Handlers, Plateloc, Janus, etc. | 11/27/2024 |
| 2096 | FlexDex Surgical Brighton, MI R&D Design Engineer Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, or equivalent Exp: 1-3 years |
To help realize our vision, we are looking to hire an experienced R&D Design Engineer with a strong background in product development, mechanical systems, and manufacturing. The candidate must have a strong understanding of processes related to design, prototype, testing, transfer of designs to manufacturing, V&V testing, and project management. In addition, experience and understanding of quality management systems is essential. | 11/27/2024 |
| 2097 | Fortrea Madison, WI On Call Clinical Research Technician Bachelor's in Science, preferred Exp: 1-2 years |
We are currently seeking a On Call Clinical Research Technician, to perform practical / administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements. Many Clinical Research Technicians are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world. | 11/27/2024 |
| 2098 | FMI Morrisville, NC Accessioning Technologist II Bachelor of Science degree in biological or life sciences Exp: 1-3+ years |
Accessioning Technologist II performs critical sample receipt and data entry functions in FMI’s CLIAcertified clinical laboratory. Specifically, the Accessioning Technologist receives all incoming samples and ensures that necessary information has been received to move forward with processing. This role is involved in both independent and collaborative work that includes the use of account or patient demographic data entry. | 11/27/2024 |
| 2099 | Fractal Therapeutics Atlanta, GA Chemical Engineer Bachelor of Chemical Engineering Exp: 1 year |
Chemical Engineer is needed in Atlanta, Georgia. Develop platforms to help clients in several pharmaceutical companies for drug development. Apply model-based techniques to improve preclinical and clinical R&D. Analyze and summarize complex pharmaceutics and PD datasets to investigate drug effects, and subsequently design the dosing strategies. Use fundamental principles to solve challenges in syntheses, process designs, and production. Develop computational fluid dynamics (CFD) models to solve the drying process in an agitated filter dryer (AFD), gas transportation in reactors, and tablet compression. Setup and perform simulations in LIGGGHTS (open-source DEM simulation software) for manufacturing of active pharmaceutical ingredients. | 11/27/2024 |
| 2100 | Fractyl Health Burlington, MA Clinical Trial Associate Bachelor’s degree in scientific field of study Exp: 1-3 years |
The Clinical Trial Associate will aid in study start up activities for Fractyl’s global clinical program, draft SSU documents, site regulatory document review and approval, and IRB/EC and regulatory submissions and approvals. Working closely with the clinical operations team members, the Clinical Trial Associate will liaise with internal and external partners to distribute continuous status updates. Main responsibilities include, but are not limited to, participating in the planning and coordination of clinical trial activities; providing project support for the initiation, execution and close out of clinical studies, working closely with internal teams and external vendors; and supporting project teams to achieve quality results in a cost‐effective and timely manner. | 11/27/2024 |
| 2101 | Fresenius Kabi Wilson, NC Associate Scientist B.S. in Chemistry, Biology or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 11/27/2024 |
| 2102 | Fresenius Kabi Wilson, NC Validation Engineer BS/BA degree in science, engineering, manufacturing technology or closely related field Exp: 1-3 years |
Responsible for providing technical support to operations in terms of equipment/system initial validation and equipment/system requalification’s. Will participate in equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. The individual must have a comprehensive understanding of cGMPs and become certified to enter Controlled Areas of the plant (Grade D, C and up to B/ A). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 11/27/2024 |
| 2103 | Freudenberg Carpinteria, CA Manufacturing Quality Engineer I Bachelor of Science Degree in Engineering or related field Exp: 0-3 years |
Participate in Measurement System Analysis activities including Gage RnR, Test Method Validations, Test Procedures, etc. as part of the Design Transfer process. Aid standardization initiatives for Quality Engineering at the site level and partners with other Freudenberg Medical facilities. Support and develop validation protocols and reports (IQ/OQ/PQ) and provide objective evidence that equipment, processes, test methods and product meet requirements and are compliant with applicable regulations. Uses statistical tools (Minitab, etc) to analyze data, make acceptance decisions, and improve process capability (Six Sigma, SPC, DOE). Assist Quality Engineering on MRB review of nonconforming products; recommends disposition and corrective actions. Performs complaint analysis investigations and trend reporting. Audit the Line’s production paperwork for accuracy; help drive the Line toward 100% first pass yield on DHR | 11/27/2024 |
| 2104 | Frontage Laboratories Secaucus, NJ Lab Technician BS in biology, chemistry, or related area Exp: 1 year |
The laboratory technician performs a variety of laboratory procedures as required by the study protocol. Laboratory technicians are responsible for assisting the Laboratory Manager, Principal Investigator, Clinical Research Coordinators, and other medical professionals in the preparation and handling of specimens, analyzing results, and maintaining laboratory equipment. Laboratory Technicians ensure accuracy, quality control, and adherence to safety protocols, contributing directly to scientific research, development of new products, or medical diagnostics. | 11/27/2024 |
| 2105 | Frontage Laboratories Exton, PA Scientist, Bioanalytical Services Master’s degree in Analytical Chemistry, Biochemistry, Pharmacology or related scientific discipline Exp: 1+ years |
Scientist / Bioanalytical Services Essential Functions Run sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. | 11/27/2024 |
| 2106 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Sr. Analyst, QC Sample Control Master’s degree in science, preferably Chemistry, Biochemistry, Microbiology, Biology, or Life Sciences relevant scientific discipline Exp: 1 year |
The Sr. Analyst, QC Sample Control works independently with limited supervision and guidance from their manager to ensure all samples managed by the Sample Control team are handled and documented in accordance with applicable internal procedures. This role is responsible for handling samples manufactured at FDB Holly Springs, samples and reference materials from external sources, coordinating stability samples and protocols within the sample control team. This role is also responsible for coordinating with key internal stakeholders on the transport of QC samples from Holly Springs to external testing laboratories and support continuous improvement projects and SOP revisions by providing input into the sample handling process. A very high attention to detail and the ability to effectively communicate and function in a fast-paced, highly technical environment is essential to success. This role is included in routine on-call and weekend support, as needed. | 11/27/2024 |
| 2107 | FUJIFILM Diosynth Biotechnologies Thousand Oaks, CA Quality Control Associate Operations Bachelor’s degree Exp: 0-3 years |
The QC Associate Operations position is responsible for executing sample management activities, which include control, receipt, and distribution of product, intermediates, raw materials samples, sample retention, reference samples, and stability samples at Fujifilm Diosynth Biotechnologies California (FDBC). The QC Associate Operations position will interact regularly with internal QC, Quality Assurance, Manufacturing, Warehouse and Facilities groups. In addition to external Quality representatives supporting client requests and/or notifications. This position is expected to carry out all their activities in compliance with FDBC Quality processes, the requirements of the Quality Management System, and in compliance with regulation requirements governing laboratory controls and manufacturing. Individuals in this role are customer service-oriented, demonstrate fundamental awareness of verbal and written communication, problem solving, critical thinking, and time management. And role model company core values of trust, delighting our customers, Gemba, and Genki. | 11/27/2024 |
| 2108 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Sr. Analyst 1, QC Chemistry M.S. in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field Exp: 1+ years |
The QC Chemistry Sr. Analyst 1 works with limited direction to execute QC analytical chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The QC Chemistry Sr. Analyst 1 adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory exceptions, invalid assays, deviations, change controls, and corrective and preventative actions (CAPAs). The role is primarily responsible for executing routine analytical methods in support of manufacturing, supporting laboratory execution of analytical method transfers and validations, and training other QC Chemistry laboratory associates. The ability to effectively communicate and function in a fast-paced, highly technical environment is essential to success. | 11/27/2024 |
| 2109 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Sr. Specialist 1, QC Lab Support Master’s degree in science, preferably Chemistry, Biochemistry, Microbiology, Biology, or Life Sciences relevant scientific discipline Exp: 1 year |
Sr. Specialist 1, QC Lab Support works under moderate supervision, supporting and participating in QC activities related to investigations, deviations, OOS/OOT, CAPAs, and Change Controls. This role assists in creating and maintaining GMP documents and processes, collaborating with stakeholders and QA. This role contributes to customer contact and CLO communication to support QC capabilities in delivering materials and results. This role helps ensure QC compliance with policies and procedures. This role participates in project management and process improvement initiatives, developing skills in risk assessment. The role requires the ability to work effectively both independently and as part of a team, with growing cross-functional collaboration. | 11/27/2024 |
| 2110 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Process Engineer 2, Chromatography and Column Packing Master’s degree in Chemical or Biotechnology Engineering Exp: No exp |
This position reports to the Process Engineering Manager, Downstream in support of the Process Equipment team for the Aura project, a greenfield construction project in Holly Springs, NC. The initial assignment is to assume the Responsible Engineer role for Chromatography and Column Packing unit operations. As the site moves into commercial operations circa 2027, this position is planned to continue as primary support for Chromatography and Column Packing unit operations, with secondary responsibility expanding to cover additional Downstream unit operations includes supporting commercial operations, technology transfers, and small capital projects. | 11/27/2024 |
| 2111 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC QA Analyst, PQS Bachelor’s Degree in Life Sciences (e.g., Engineering, Applied Science or Chemistry) Exp: No exp |
The QA Analyst, PQS assists in the quality oversight of PQS applications for the Enterprise Quality Systems administration and document control. The QA Analyst collaborates within the team as well as with other project teams on-site, and with QA departments at other FDB sites. This role focuses on consistent policy administration, assists QA oversight of daily activities, and resolves or mitigates issues that occur during operations. This role maintains relationships with site-based customers and global colleagues, and provide updates as requested. | 11/27/2024 |
| 2112 | FUJIFILM Diosynth Biotechnologies Thousand Oaks, CA Manufacturing Associate Bachelor of Science (B.Sc.) Exp: 0-3 years |
The Manufacturing Associate works as part of the manufacturing team to deliver high quality cell therapy materials during process transfers, routine production, and technology improvements. This position contributes to the successful delivery of released product in support of clinical trials and commercial production. | 11/27/2024 |
| 2113 | Galen Robotics Baltimore, MD Manufacturing/Sustaining Engineer Bachelor’s Degree in engineering Exp: 1-3 years |
The Manufacturing/Sustaining Engineer will focus on providing the highest level of engineering support for devices being developed and installed in the field and support ongoing sustaining engineering projects. Other daily responsibilities to include support of development team, contract manufactures along with providing support to R&D projects as requested. | 11/27/2024 |
| 2114 | GenEdit South SF, CA Research Associate, In Vivo Bachelor’s degree Exp: 1 year |
GenEdit is seeking a highly motivated and goal-oriented Research Associate with hands-on experience in performing in vivo studies to join our team. This full-time position will report to the Group Lead – In Vivo and will be responsible for testing nanoparticle encapsulated gene therapeutic drugs in vivo and related in vitro analysis of tissues and cells. Additional duties and responsibilities may be required as needed. The successful candidate will be a highly collaborative, resourceful, and effective team-player who is enthusiastic about tackling challenging complex scientific and technical problems with novel approaches and solutions. | 11/27/2024 |
| 2115 | Genezen Indianapolis, IN AD Lab Associate I/II BS or MS degree in Biology, Biochemistry, Molecular Biology, or similar field. Exp: 1-5 years |
We are looking for someone with high emotional intelligence and is comfortable working closely across the team to join us in facilitating the production of viral vectors. The Laboratory Associate I/II will be needed to perform analytical assays for viral vector process development, assist with method development, document experiments, help with lab maintenance and execute assay qualifications. This position calls for an independent thinker who can work seamlessly in a matrixed environment. | 11/27/2024 |
| 2116 | Genezen Lexington, MA Manufacturing Technician II BS degree in Life Sciences/Engineering Exp: 1+ years |
With general supervision the individual will perform routine and non-routine manufacturing operations, including but not limited to work functions in Cell Culture, Purification, Solution & Equipment Prep areas. Operates production equipment according to SOPs to produce clinical and/or commercial products. Independently perform manufacturing of Genezen’s therapeutic products and ensure this is realized and documented according to the highest industrial and GMP quality requirements This individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Batch Production Records and Solution prep records. | 11/27/2024 |
| 2117 | Genezen Lexington, MA Process Development Lab Technician B.S. degree in Biology, Biochemistry, Molecular Biology, or similar field Exp: 1+ years |
The Process Development Lab Technician will support the development and optimization of viral vector processes at Genezen’s Lexington site in MA. This role involves assisting with upstream and/or downstream process development activities, including cell culture, fermentation, purification, and formulation. The ideal candidate will demonstrate a strong enthusiasm for learning and developing new skills. This position requires a detail-oriented individual with the resilience to thrive in a fast-paced, dynamic environment and a commitment to maintaining high standards of safety and compliance. | 11/27/2024 |
| 2118 | Genezen Lexington, MA Process Engineer I, Manufacturing Sciences & Technology Bachelor's or Master's Degree in Engineering Exp: 0-3 years |
The Manufacturing Sciences & Technology (MSAT) group plays a critical role in successful manufacturing of clinical and commercial products. The person in this role assists the MSAT team in the transfer of technologies, process validation and cGMP manufacturing of Genezen’s gene therapy products. This individual will contribute as a core member of various cross-functional teams, and interacts extensively with other departments within Genezen including Process Development, Manufacturing, Engineering, Quality, and Regulatory Affair etc. | 11/27/2024 |
| 2119 | Genezen Lexington, MA Validation Engineer I/II Bachelor's Degree in Engineering Exp: 0-8 years |
The incumbent is responsible for assisting the Validation manager in completion of all project milestones. This includes installation, operational and performance qualification of equipment and utilities, environmental qualification, process validation, and preparation of all relevant documentation to meet regulatory requirements for new and existing products (includes standard operating procedures, technical reports and risk assessments). Duties require some knowledge in the pharma/biotech field. | 11/27/2024 |
| 2120 | GenScript Biotech Pennington, NJ QC Associate Scientist Bachelor’s degree in Molecular Biology, Biochemistry, Microbiology or related scientific field. Exp: 1-2 years |
The position reports to the Sr. QC Manager, is ideally suited for a professional with technical knowledge, and exposure to developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to learn this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients. | 11/27/2024 |
| 2121 | GenScript Biotech Pennington, NJ Bioprocess Specialist-Upstream Processing Bachelor’s degree in science or engineering Exp: 0-5 years |
The Technician/Specialist, Bioprocess – Upstream Processing will work within the Upstream Processing group and performs the following activities while executing upstream operations: Preparation of stock solutions, buffers and media. Filtration of stock solutions, buffers and media. Set-up and operate disposable fermenters / bioreactors and other disposable bioprocess equipment including depth filtration. Passage and expansion of microbial and mammalian cell lines. The Technician/Specialist, Bioprocess – Upstream Processing supports relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 11/27/2024 |
| 2122 | GenScript Biotech Pennington, NJ Bioprocess Specialist, Downstream Processing Bachelor’s degree in science or engineering Exp: 0-5 years |
The Bioprocess Specialist works within the Downstream Processing group. The Bioprocess Specialist will perform the following activities while executing downstream operations: Preparation of solutions, Filtration, Chromatography, Tangential flow filtration, Homogenizing, Drug substance formulation, Drug product formulation, Drug product vial filling. The incumbent works cross-functionally with internal departments and external resources on gene therapy manufacturing related issues. | 11/27/2024 |
| 2123 | Getinge Wayne, NJ Quality Engineer I Bachelor’s degree in engineering, Science, or other related field is required. Exp: 1 year |
As a Quality Engineer I specializing in Quality Operations, you will be responsible for overseeing and improving the quality of manufacturing processes, ensuring compliance with regulatory requirements, and driving continuous improvement initiatives to enhance product quality and customer satisfaction. You will play a key role in ensuring that our manufacturing operations meet the highest standards of quality and efficiency while adhering to relevant regulations and industry best practices. | 11/27/2024 |
| 2124 | GigaGen South SF, CA Senior Research Associate Masters degree in Life Sciences or related discipline Exp: 1 year |
We are seeking a talented and highly motivated Senior Research Associate to support our diverse antibody therapeutics pipeline. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 11/27/2024 |
| 2125 | GigaGen South SF, CA Research Associate Bachelor’s degree in Life Sciences or related discipline Exp: 1+ year |
We are seeking a talented and highly motivated Research Associate to support our diverse antibody therapeutics pipeline. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 11/27/2024 |
| 2126 | Gilead Foster City, CA Sr Research Associate Protein Therapeutics M.S. Exp: 0+ years |
The Molecular Assessment group within the Protein Therapeutics department is looking for a talented and motivated senior research associate to join our team. For this laboratory-based role, the successful candidate will be mainly responsible for generating high quality molecular assessment data for a variety of early-stage biologics candidates using analytical methods. If you are passionate about developing new biologics and eager to grow and learn in an exciting and fast-paced environment, we encourage you to apply for this job. | 11/20/2024 |
| 2127 | Gilead Foster City, CA Research Associate- In Vivo Pharmacology BS Exp: 0-2 years |
We are seeking a highly motivated Research Associate to join our Oncology in vivo pharmacology team. The selected candidate will be responsible for evaluating novel oncology therapeutics in pre-clinical mouse oncology models. Hands on experience with pre-clinical mouse models is required. The successful candidate will be responsible for designing, generating and communicating pharmacology data to support the progression of oncology research programs. Title will be commensurate with experience. | 11/20/2024 |
| 2128 | Gilead Foster City, CA Sr Research Associate I - Pre-Pivotal Biologics Analytical Operations M.S. Exp: 0 years |
Gilead Sciences (Foster City, CA) is seeking a talented and highly motivated Senior Research Associate I to join our Pre-Pivotal Biologics Analytical Operations group. Our collaborative and interdisciplinary development team utilizes state-of-the-art technologies and innovative methodologies to advance medicines into the clinic. S/he will have opportunities for career growth through acquisition of new skills, experiences, and professional relationships in a fast-paced and resource-rich environment. | 11/20/2024 |
| 2129 | Gilead Foster City, CA Senior Research Associate I–Pre-Pivotal Biologics Development M.S. Exp: 0+ years |
Gilead has an opportunity for an industry experienced level scientist in the Cell Line Development (CLD) group at our Foster City campus facility. We are seeking a highly motivated, team-oriented individual to design and execute experiments to support cell culture and clone development for our rapidly growing biologics pipeline. The successful candidate will also contribute to the overall strategy of new technology development projects. | 11/20/2024 |
| 2130 | CytoSorbents Princeton, NJ Process Operator/Production Associate Bachelor of Science degree with Science major Exp: 0 years |
CytoSorbents is seeking a Manufacturing/Production Associate to work 2nd shift (2:00 – 10:30 pm) in Princeton, NJ. The Manufacturing/Production Associate will perform GMP activities associated with producing, cleaning, and packaging of CytoSorb®, a unique blood purification medical device used to control deadly inflammation in life-threatening illnesses in the ICU and cardiac surgery. Come join us in saving lives! | 11/20/2024 |
| 2131 | Day Zero Diagnostics Boston, MA Laboratory Technician, Molecular Assay Development Bachelor's degree in a chemical, physical, biological, or clinical laboratory science Exp: 1 year |
The Laboratory Technician will play an essential role in the operational side of the lab as well, as directly performing experimentation as part of the research and development team. The Lab Technician will be responsible for maintaining materials, reagents, bacterial stocks, waste streams, and lab cleanliness. In addition, they will assist with experimentation; strictly adhering to lab SOPs in the processing of laboratory samples and recording and communicating their results. | 11/20/2024 |
| 2132 | Day Zero Diagnostics Boston, MA Laboratory Technician II, Sequencing Technologies Bachelor's degree in a chemical, physical, biological, or clinical laboratory science Exp: 1-2 years |
Day Zero Diagnostics is seeking a Laboratory Technician II to support the Sequencing Technologies team. This candidate is responsible for daily high-throughput sample processing, conducting DNA library preparation, quality control (QC) assessments, and whole-genome sequencing (WGS) on both short- and long-read platforms with minimal guidance. They will handle reagent preparation and project-specific inventory while strictly following SOPs, meticulously documenting processes and delivering high-quality, timely results. Located in DZD’s new, state-of-the-art facility in Watertown, MA, this role provides opportunities for developing skills surrounding training, logistics, and data analysis in addition to wet lab developmen | 11/20/2024 |
| 2133 | Mammotome Cincinnati, OH Service Engineer Bachelor’s Degree in an engineering discipline Exp: 1 year |
The Service Engineer for Mammotome is responsible for improving the post-purchase experience of clinicians supporting breast cancer patients. You will champion continuous improvement throughout service operations, be a key contributor to EU & APAC service projects, and serve as the technical expert on aftermarket support for Mammotome capital products. This position is part of the Aftermarket Service and Solutions team located in Blue Ash, Ohio and will be an ONSITE position. At Mammotome, our passion is driving innovative technologies that create efficiencies, while never forgetting that at the heart of every breast cancer journey is a patient. You will be a part of the Service Support team and report to the Sr Manager, Global Sales Operations and is responsible for customer issue to resolution process. If you thrive in a fast paced, supporting, and problem solving role and want to work to build a world-class technical service organization—read on. | 11/20/2024 |
| 2134 | Dexorgen Rockville, MD Biological Technician MS in Biology or Chemistry Exp: No exp |
Perform biological technician duties in helping biological scientists conduct laboratory tests and experiments. | 11/20/2024 |
| 2135 | Diacarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science Exp: 0-1 years |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 11/20/2024 |
| 2136 | Diacarta Pleasanton, CA Research Associate BS degree in molecular biology or a related field Exp: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 11/20/2024 |
| 2137 | Diacarta Pleasanton, CA Manufacture Technician BS. degree in Molecular Biology, Cell Biology, Biotechnology or related field Exp: 1 year |
This position is a member of a fast-paced production team and will be responsible for the following tasks. Purchase raw materials from a vendor. Receive incoming materials and perform inspection and inventory recording. Production of DiaCarta IVD products to meet sales demands. Labeling of raw materials and finished goods. Perform calibration or preventative maintenance of the instrument. Participate in process improvement projects. Compliance with corporate quality systems. Other on-the-job assignments indicated by management | 11/20/2024 |
| 2138 | Difgen Pharmaceuticals Tamarac, FL Analyst, Microbiologist I B.S. or M.S. in microbiology or equivalent Exp: 1-2 years |
The QC Microbiologist I performs microbiological testing of DI water, intermediate/finished products, and environmental bio-burden. He/She maintains a functional and current GMP compliant microbiology laboratory. | 11/20/2024 |
| 2139 | Eurofins Tustin, CA Chemist I - VOA GCMS BS or BA in chemistry or related field Exp: 1+ years |
Eurofins Environment Testing Southwest - Tustin CA is searching for a VOA GCMS chemist to prepare and analyze environmental samples following EPA protocols in adherence with Eurofins Quality Assurance programs and SOP’s. | 11/20/2024 |
| 2140 | Eurofins Spring House, PA Bioanalytical Scientist B.S./B.A. in Molecular Biology, Immunology, Cell Biology, Biology, Biochemistry, Biology, or related biological science discipline Exp: 1 year |
Develop and qualify cell-based or ligand-binding based bioanalytical assays to support high priority biological and vaccine programs. Analyze samples using multiple platforms such as Luminex, MSD, ELISA, or cell-based assay. Assess acceptability of analytical result data using LIMS or other computer software. Basic data assembly and visualization using Excel, Spotfire, and/or GraphPad. Work according to established Standard Operating Procedures (SOPs) and regulatory guidance. Maintain accurate records of ongoing projects in adherence with regulated documentation standards. Assist in generation and review of reports and contribute to trouble shooting efforts. Collaborate and communicate within and across the working group. Work in a structured environment under direct to moderate supervision. Adhere to GLP regulations and safety requirements in BSL-2. | 11/20/2024 |
| 2141 | Eurofins Cary, NC PLM Analyst BS or BA in a closely related science Exp: 1-2 years |
The Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 11/20/2024 |
| 2142 | Eurofins Pasadena, TX PLM Analyst BS or BA in a closely related science Exp: 1-2 years |
The PLM Analyst prepares and analyzes environmental samples according to the required methodology and company compliance. As an analyst you will gain experience of both job-specific routine and complex analyses. The analyst team also validates and reviews data for accuracy, uploads laboratory data into the LIMS system, and ultimately will prepare and generate required reports to our clients. As a member of our analyst team you will also oversee sample scheduling and work to meet sample due dates and hold times. | 11/20/2024 |
| 2143 | Eurofins Fort Lauderdale, FL Asbestos Analyst Bachelors degree in Microbiology, Biology, Geology or a closely related science. Exp: 1-2 years |
The Analyst performs analysis of bulk samples for asbestos using polarized light microscopy. Analysis of non-culturable surface and air samples for fungi is a plus but not required. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS and reports to clients. Schedules sample workload according to due dates and sample hold times and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 11/20/2024 |
| 2144 | Eurofins Rensselaer, NY Chemistry Data Review and Technical Writing Associate Bachelor's degree in life sciences (Chemistry or Biochemistry major) Exp: Entry Level |
Eurofins is seeking a self-motivated, adaptable, and positive individual who can work both independently and as part of a team in a client facing environment. The primary purpose of this position is to perform analysis of manufacturing data from chromatography and other purification processes. Investigations will be performed to identify root cause and path forward for any out of trend data. Presentations will then be created to provide recommendations for actions when necessary. Troubleshooting equipment and processes, maintaining clean orderly work spaces, and ensuring compliance are all responsibilities of this role. Completes laboratory documentation and reviews logbook data. Complies with all pertinent regulatory agency requirements and maintains inspection readiness. Occasional opportunities for preparation and operation of chromatographic systems for small scale lab experiments. After completion of the experiments, data and statistical analysis will be completed to understand relationships and impacts to processes | 11/20/2024 |
| 2145 | Eurofins Columbia, MO Scientist II - Bioassay Bachelor’s degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related Exp: 1-3 years |
Eurofins BPT-Columbia is looking for a Scientist to join our growing Bioassay team located in Columbia, Missouri. The Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments. | 11/20/2024 |
| 2146 | DNAe Carlsbad, CA Associate Scientist Master of Science in Biology or related Exp: 1 year |
Research and study cellular molecules to develop an infectious disease molecular assay with knowledge of real-time PCR and NGS workflows. Perform nucleic acid extraction from human sample including whole blood. Perform experiments and procedures in accordance with guidance from supervisor or from written protocols. Documenting, reporting, and presenting results of experiments and procedures. Following work instructions and SOPs, documenting procedures as required by ISO 13485 quality management systems. Assisting in maintaining laboratory supplies and equipment. | 11/20/2024 |
| 2147 | Dragonfly Therapeutics Waltham, MA Associate Scientist II/Sr. Associate Scientist M.Sc. in Biochemistry, Biochemical Engineering, Chemistry, or related discipline Exp: 1-4 years |
Dragonfly Therapeutics is seeking an Associate Scientist II / Senior Associate Scientist to join our team (Title commensurate with experience). Responsibilities include providing biophysical and biochemical characterization of our candidates to inform lead selection, performing developability assessments, interpreting and summarizing results, authoring technical reports, representing the Protein Sciences function on cross-functional teams. The candidate must be independent, goal-oriented, flexible, and able to work efficiently across multiple projects. We are searching for enthusiastic and innovative individuals with a keen eye for detail, who thrive in a fast-paced, entrepreneurial environment. | 11/20/2024 |
| 2148 | Eclipse Bioinnovations San Diego, CA RNA Platform Manager MSc in Molecular / Cell Biology or related discipline Exp: 1 year |
We are looking for an RNA Platform Manager to join our team to support eMERGE, our partnership platform for RNA-based medicine success. This is role will be responsible for developing and maintaining partnerships with academics, biotechs, and biopharmas that are developing the next generation of vaccines and therapies. You will work with our Marketing and Sales teams to identify new areas for growth and to present on our capabilities to potential partners. You will also work with our Core and Custom Solutions teams to draft project proposals and statements of work to ensure that each partnership is a success. The ideal candidate will be excellent at presenting, well-organized, and passionate about the power of RNA to revolutionize medicine. | 11/20/2024 |
| 2149 | eGenesis Greater Madison, WI Quality Control Microbiology Specialist B.S./M.S. in Life Sciences or related field Exp: 0-3 years |
eGenesis is seeking an innovative QC Microbiology Specialist to lead and provide the technical and strategic oversight of eGenesis’ environmental monitoring program. In this position you will be responsible for hands on environmental monitoring sampling, testing, reporting and trending of eGenesis’ two GMP manufacturing facilities (Greater Madison Area and Northwest Indiana). You will ensure activities are executed in a cGMP compliant manner and will work collaboratively on implementation and maintenance of our contamination control program. The ideal candidate will be independently motivated, a strong communicator and demonstrate proficiency in regulatory compliance. This position will be an onsite position in the Greater Madison Area. | 11/20/2024 |
| 2150 | Elektrofi Boston, MA Engineer III M.S. in Chemical, Biomedical, Materials, or Pharmaceutical Engineering, or a related engineering discipline Exp: 1 year |
Elektrofi is seeking a motivated individual to join our biotech company as an Engineer III to support process development of the novel Elektrofi formulation platform. The individual will join a growing, multidisciplinary team of scientists/engineers and industry professionals. | 11/20/2024 |
| 2151 | Elutia Silver Spring, MD Research & Development Engineer PhD in life sciences, chemistry, material sciences, biomedical engineering or related field Exp: 1-3 years |
The R&D Engineer at Elutia is responsible for designing and developing biological-based medical devices, specializing in drug/device combination products according to industry standards. This role encompasses overseeing the entire development process, from initial concept through to commercialization. The R&D Engineer leads prototype and pilot production, develops and executes test methods, and collaborates with cross-functional teams to advance Elutia’s product pipeline. They ensure seamless product development and facilitate tech transfer for successful clinical and commercial use by applying critical thinking skills to solve technical issues. Additionally, the R&D Engineer contributes to the intellectual property portfolio and ensures compliance with regulatory requirements to gain product approvals and support product lifecycle management. The successful candidate will work onsite at the Company’s Silver Spring, MD facility. | 11/20/2024 |
| 2152 | Emerald Cloud Laboratory Austin, TX Laboratory Operator I, II, & III Bachelor’s degree Exp: 1-3 years |
The demand for our service is growing, and to meet that demand, we are recruiting Lab Operators looking to explore opportunities in the biotech space and grow with our organization. Qualified candidates will receive comprehensive lab and safety training, allowing them the ability to run protocols in our Austin facility. These protocols are critical to sustaining the high-quality operations of the facility and provide experience working in ECL’s unique, process-driven lab environment with our integrated software tools. | 11/20/2024 |
| 2153 | Empirico Madison, WI Assistant Scientist - Drug Discovery Bachelor’s degree in Molecular Biology, Biochemistry or a related discipline Exp: 1 year |
Empirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines, is looking for a talented scientist to join our Drug Discovery team and help advance our growing pipeline. This is an excellent opportunity to make meaningful contributions to the discovery and validation of novel therapeutic targets. You will work closely with other scientists that have a passion for finding new approaches toward the treatment and prevention of disease. Your responsibilities will include performing different bioanalytical assays intended to provide key study readouts around biodistribution, pharmacokinetics, and pharmacodynamic biomarkers. The ideal candidate will have experience in both protein- and nucleic acid-based assays, be highly organized, and enjoy working in a team environment. | 11/20/2024 |
| 2154 | Endo Rochester, MI Quality Associate Specialist, Product Release BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 11/20/2024 |
| 2155 | Endo Rochester, MI Microbiologist II Master of Science degree in microbiology, biology or related field Exp: 1+ years |
The Microbiologist II performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 11/20/2024 |
| 2156 | Endo Rochester, MI Process Engineer I MS degree in Engineering or Chemical Engineering Exp: 1+ years |
The Process Engineer I, with guidance, performs various duties related to optimization and analysis of production processes, new products, processes and technology transfers. Prepare and execute engineering study protocols, manufacturing and packaging experimental / feasibility study / validation batch records and protocols and complete interim and / or final summary reports for marketed and new products. Perform or assist on-site and site-change technical transfer, scale-up or scale-down factor evaluation, manufacturing / packaging process and equipment troubleshooting, and SOP preparation and review. | 11/20/2024 |
| 2157 | Endo Rochester, MI Chemist II, Quality Control Laboratory Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 11/20/2024 |
| 2158 | Endotronix Naperville, IL Quality Engineer I - Failure Analysis BS in Engineering (prefer Electrical or Biomedical) Exp: 0-1 years |
As a Quality Engineer in Failure Analysis you will be responsible for supporting various elements of the Quality System such as Complaint investigations, Non-Conformance Investigations, and general failure analysis. | 11/20/2024 |
| 2159 | Endotronix Naperville, IL Technical Product Engineer I Bachelor's degree in Electrical, Computer Science, Biomedical, Mechanical, or Reliability Engineering Exp: 1-2 years |
The Technical Product Engineer will take the lead in troubleshooting advanced technical support issues in the field that are escalated by the customer support team. This will include the intake, investigation, documentation, and resolution of complaints and other field issues. Troubleshooting will include investigating failures, identifying root causes, and providing resolutions for the end user. The engineer will work closely with R&D and use data analysis tools (MATLAB, Python, Minitab etc.) to analyze field, vendor, and internal test data as an aid in the troubleshooting process. Acting as a technical lead, they will provide feedback to R&D and manufacturing which can be used to initiate corrective action and/or reliability improvements. | 11/20/2024 |
| 2160 | Endotronix Naperville, IL Manufacturing Engineer I BS in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, Computer Engineering or equivalent. Exp: 0-3 years |
This Manufacturing Engineer I is primarily responsible for developing and controlling the manufacturing process for the Cordelia System and Cordella Pulmonary Artery Sensor System (Cor PASS). | 11/20/2024 |
| 2161 | Epigen Biosciences San Diego, CA Senior Research Associate/Research Associate - Chemistry MS/BS in synthetic organic chemistry or related field Exp: 1+ years |
Experience with modern synthetic organic chemistry, purification, and analysis is required. Experience with using ChemDraw/Reaxys/SciFinder. Performance of routine synthesis of heterocyclic compounds in milligram to multi-gram scale to support lead identification and optimization and record-keeping. Performance of purification of synthesized compounds using prep-TLC, silica gel/C18 column chromatography. Performance of and analyzing compounds using NMR spectra and LCMS. Performance of Microsoft Office tools such as Word, Excel, PowerPoint and Outlook. Good communication and presentation skills to effectively work with cross-functional groups with diverse background and interests. Strong attention to detail, excellent written and oral communication skills. Ability to work with a team of individuals to meet goals | 11/20/2024 |
| 2162 | Epigen Biosciences San Diego, CA Senior Research Associate/Research Associate - Biology MS/BS in biology or related field Exp: 1+ years |
Experience with cell culture and cell-based in vitro assays is required. Experience with the development and optimization of in vitro biological assays is required. Performance of routine assays to support lead identification and optimization. Performance of molecular biology techniques, such as Western blotting and transient transfection. Performance of data analysis, reporting and record keeping. Performance of Microsoft Office tools such as Word, Excel, PowerPoint and Outlook. Good communication and presentation skills to effectively work with cross-functional groups with diverse background and interests. Strong attention to detail, excellent written and oral communication skills. Ability to work with a team of individuals to meet goal. | 11/20/2024 |
| 2163 | Evonik Allentown, PA Lab Technician BS Exp: 1 year |
The position exists to support lab experimentation associated with the conceptualization, synthesis development and transfer of lab scale procedures to the engineering team for scale up development. The incumbent will be involved in lab operations including chemical synthesis, purification and analysis. The candidate will be required to function effectively independently and in work teams. The position is responsible for safe operation of their lab unit and thorough documentation of observations and results. The position exists to support lab experimentation associated with the conceptualization, synthesis development and transfer of lab scale procedures to the engineering team for scale up development. The incumbent will be involved in lab operations including chemical synthesis, purification and analysis. The candidate will be required to function effectively independently and in work teams. The position is responsible for safe operation of their lab unit and thorough documentation of observations and results. | 11/20/2024 |
| 2164 | Evonik Birmingham, AL Maintenance Quality Engineer Bachelor of Science Degree in an Engineering discipline, preferably Mechanical or Chemical or other stem related field Exp: 1-3 years |
This position will be the primary owner of Facilities department Quality programs, including management of change, deviation investigations, and implementation of corrective / preventive actions stemming from audits and quality-related incidents. As program owner, this position will be responsible for on-time closure of all Quality records, via both direct execution by this position and by assisting / coordinating other positions in the department with their assigned records. Additionally, this position serves as the technical lead on maintenance topics related to development-scale equipment such as reactors, homogenizers, etc. The Maintenance Quality Engineer will identify critical spare parts, develop maintenance work instructions for technicians to execute, and directly assist technicians with execution and troubleshooting. Finally, this position will help drive the desired “utilities as processes” mentality by tracking and reporting daily utility (steam, water, etc.) data, analyzing for outliers, and proposing improvement actions. | 11/20/2024 |
| 2165 | Evonik Birmingham, AL QC Associate Scientist Bachelor’s degree in Chemistry or other relevant science. Exp: 0-3 years |
The Quality Control Associate Scientist performs accurate and timely testing of routine lab samples in accordance with appropriate GMP and safety guidelines. The Scientist will also perform equipment qualifications and quality system improvement initiatives by executing well-defined protocols and procedures. | 11/20/2024 |
| 2166 | Nanoimaging Services San Diego, CA Account Manager, Nanoparticle Sales None Exp: 0 yrs |
Reporting to the Head of Nanoparticle Characterization Sales, this role will work closely with the scientific and operations teams to help provide high-quality cryo-TEM Nanoparticle Characterization services to our clients. Key responsibilities include generating proposals, managing purchase orders, logging client interactions in our CRM, and providing day-to-day account support to maintain strong client engagement. This role is ideal for someone eager to build experience in account management and collaborate within a high-performing team. | 11/14/24 |
| 2167 | Charles River Wayne, PA Technician II – Analytical Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 1-3 years |
Perform routine analytical methods independently as specified in standard in-house SOPs, Client Test Methods and other written procedures. | 11/11/2024 |
| 2168 | Charles River Wayne, PA Technician II – BioPhysical Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 1-3 years |
Perform routine biophysical methods independently as specified in standard in-house SOPs, Client Test Methods, and other written procedures. Under direct supervision, perform method development work as assigned. | 11/11/2024 |
| 2169 | Charles River Wayne, PA Technician I – Analytical Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 0-2 years |
Under direct supervision, perform Routine analytical methods as specified in standard in-house SOPs Client Test Methods and other written procedures. | 11/11/2024 |
| 2170 | Charles River Wayne, PA Technician I – BioPhysical Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 0-2 years |
Under direct supervision, perform biophysical methods as specified in standard in-house SOPs, Client Test Methods, and other written procedures. | 11/11/2024 |
| 2171 | Charles River Malvern, PA Technician II Mammalian Cell Banking Bachelor’s degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 1-2 years |
Under direct supervision, responsible for performing basic daily laboratory and clean room tasks as they relate to the operations performed within the Manufacturing department, including mammalian cell banking and vaccine preparation activities, data analysis and writing client batch records and SOPs. | 11/11/2024 |
| 2172 | Charles River Wayne, PA Technician I Environmental Monitoring and Contamination Control Bachelor’s degree (B.S.) or equivalent in biology or related discipline Exp: 0-1 years |
Responsible for performing daily laboratory tasks as they relate to the Environmental Monitoring and Contamination Control Department. | 11/11/2024 |
| 2173 | Charles River South SF, CA Research Associate I B.S. or M.S. in biology or related field Exp: 1-2 years |
We are looking for a Research Associate I to join our Insourcing Solutions team located in South San Francisco, CA. Mammalian cell culturing, including media preparation, cell line maintenance, plating, and transfection. Molecular biology tasks including but not limited to molecular cloning, DNA/RNA extraction from animal tissue and cultured cells, basic immunofluorescence assays, DNA library construction, ELISA, PCR, qPCR, ddPCR and Western blotting. Confidently conducting and troubleshooting assays and experiments in a research production environment with guidance from management. Participate in group meetings and present collated data packages for feedback and review. Maintaining detailed notes of experimental results, participation, and presentation of results at team meetings. Assisting with laboratory housekeeping tasks, including receiving, maintaining, and cataloging constructs and reagents. Complying with all laboratory safety procedures. | 11/11/2024 |
| 2174 | ChemGenes Wilmington, MA Senior Research Support Associate B.S. degree in Biochemistry, Biology or related field Exp: 0-2 years |
Manufacture of synthetic DNA & RNA compounds. Assist with experiments supporting research in the synthesis of single-cell-barcoded beads, quality control of the synthesized beads, and performing experiments that include basic molecular biology techniques to sequencing experiments to validate and troubleshoot synthesis of DNA oligos to beads. Provide comprehensive technical support for scientists in the company; executing and optimizing ongoing experiments, analyzing results and designing follow-up experiments based on the results, and presenting findings and insights at group meetings. Evaluating research methods, procedures and techniques based on established objectives, conceiving and designing basic experimental protocols to ensure project completion in a timely fashion; recording and organizing data generated from the experiments in clear, concise, and assessable format; perform basic coding and statistical analyses; processing of in-vitro and in-vivo RNA for preparation of RNA-seq libraries for sequencing in Illumina platforms (Mi-Seq including Hi-seq and Next-seq). Experienced in techniques including but not limited to: running agarose gel, polyacrylamide gel electrophoresis, reverse transcription, quantitative PCR, fluorescent microscopy, flow cytometry; maintaining inventories of lab stocks. | 11/11/2024 |
| 2175 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: 1 year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 11/11/2024 |
| 2176 | Cipla Fall River, MA Quality Control Chemist Level 1 Bachelor's degree (BS or BA), in Chemistry, Biology, Pharmaceutical Sciences, or related field Exp: 0-3 years |
The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience, or a combination of all three. | 11/11/2024 |
| 2177 | Cipla Central Islip, NY QC Chemist III Master of Science Degree Chemistry, Pharmaceutical Sciences, or related field Exp: 1 year |
Perform analytical testing for Raw Materials, Finished and In-Process of Drug Substances and Products like Related Compounds, Assay, Content Uniformity, Dissolution, Blend Uniformity, Karl Fischer Titration, and other related Physical testing for the methods using instruments HPLC, UV/VIS, Dissolution (USP-I, II & III) and FTIR. Execute Method validations of Drug Substance and Drug Products including Related Compounds, Assay, Dissolution, Content Uniformity, Blend Uniformity as per ICH guidelines/USP /FDA requirements. Collaborative team player with excellent communication skills working in a highly dynamic, cross disciplinary environment. Develop efficient and selective analytical procedures and draft/review laboratory SOP’s. Identify discrepancies, initiate, and investigate OOS/OOT results. Perform timely and accurate peer review of analytical test results report/document in notebooks. Maintain QC lab related systems to ensure compliance with industry standards. | 11/11/2024 |
| 2178 | Cirtec Medical Brooklyn Park, MN Quality Systems Engineer I Bachelor’s Degree Exp: 0 years |
The Engineer, Quality Systems position will be responsible for ensuring operational adherence and compliance to Cirtec Medical’s Quality Management System (QMS) requirements. This role will be expected to provide input on, and contribute to, development and implementation of Quality System improvement strategies and approaches. | 11/11/2024 |
| 2179 | Clasp Therapeutics Rockville, MD Research Associate/Senior Research Associate; Antibody Discovery and Characterization BS/MS degree in biology, biochemistry, chemistry, genetics or related disciplines Exp: 0-2 years |
The Antibody Discovery and Characterization Research Associate is a key role in our discovery pipeline and an excellent opportunity for career development within a fast-paced, collaborative environment. You will help to lead the discovery and characterization of antibodies utilizing phage display libraries and optimizing biologic therapeutics towards developability and specificity. You will be a motivated, collaborative and innovative scientist with a proven ability to solve complex problems and manage successful technology transfer working with our internal analytical development and process development group, as well as CDMOs while helping to establish and build out the antibody/protein engineering group. This position offers a unique opportunity to bring automation and high throughput approaches to classical biochemical and molecular biology problems with the goal of discovering truly cancer-specific and life changing therapeutics. | 11/11/2024 |
| 2180 | CMIC Group Hoffman Estates, IL Research Analyst Bachelors in Chemistry, Food Science, Engineering, Food Technology or related field Exp: 1 year |
The Research Analyst will perform lab activities in accordance with applicable Methods, Plans, SOPs/SWPs, GLP regulatory guidelines and 21 CFR Part 11 as directed from Group Leader and Sr. Analysts. Conduct Bio-analysis validation and sample analysis independently. Conduct Pre-Study with minimal supervision. Utilize establish techniques to compile and analyze data. Document work and maintain study documentation and lab records. Provide direction and technical assistance to lesser-skilled team members. Assist with SOP/SWP preparation and other technical related documents including client communications. Perform other routine laboratory duties as deemed necessary. Maintain a safe environment. | 11/11/2024 |
| 2181 | Coastar Therapeutics San Diego, CA Research Associate II M.S. or B.S. degree Exp: 1- years |
Coastar Therapeutics is currently seeking a talented and highly motivated research associate with molecular biology background to join the multidisciplinary R&D team. The candidate will be responsible for designing and executing experiments in support of the biological membrane coated virus development. The candidate will also be involved in developing and validating collaborating projects to support Coastar’s fast-growing preclinical pipelines. The successful candidate must demonstrate broad and in-depth knowledge of molecular biology techniques. This is a full-time position reporting to the CSO and is located at our corporate headquarter in San Diego. | 11/11/2024 |
| 2182 | Compugen South SF, CA Research Lab Technician Bachelor’s degree in life sciences Exp: 3-6 months |
The research technician will support ex-vivo and in-vitro experiments, as a part of the functional validation of immunomodulatory molecules discovered by Compugen. The research work under the supervision of scientists will include expression studies in human and mouse tumor-infiltrating immune cells, and functional immune assays for elucidation of mode of action. | 11/11/2024 |
| 2183 | Concuir Los Angeles, CA Project Engineer I and II BS Engineering degree required, Chemical, Mechanical or Biomedical Exp: 1-3+ years |
As a full-time employee of Concuir, Inc, you will provide consulting services to pharmaceutical, biotech and/or medical device manufacturing clients. In this role, you will quickly learn common client practices, recommend and implement improvements to reach project goals, and have the opportunity to scale-up and bring new products into manufacturing. You will be able to utilize your experience as well as benefit from Concuir’s portfolio of project management and cGxP best practices to drive your overall success. Projects range from design through qualification of production equipment, utilities modification, implementation of new facilities and process scale ups. | 11/11/2024 |
| 2184 | Confluent Medical Technologies Laguna Niguel, CA Process Development Engineer I BS degree in engineering Exp: 0-3 years |
Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers. We are looking for a Process Development Engineer I to join our Laguna Niguel, CA team. | 11/11/2024 |
| 2185 | Contract Pharmacal Corp Hauppauge, NY Chemist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Chemist is responsible for and has experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Microbiology, ICP, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 11/11/2024 |
| 2186 | Contract Pharmacal Corp Hauppauge, NY Scientist I; Analytical R&D Bachelor’s or Master’s degree in chemistry or analytical chemistry Exp: 1-2 years |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. | 11/11/2024 |
| 2187 | Cook Medical Bloomington, IN Senior Material Scientist Master of Science degree in Materials Science or Polymer Science Exp: 1 year |
Support pre/post-market engineering by solving material problems to develop and improve medical devices and manufacturing processes and advance the strategic goals of the company. | 11/11/2024 |
| 2188 | Cook Medical Bloomington, IN Senior Material Scientist Master of Science degree in Materials Science or Polymer Science Exp: 1 year |
Support pre/post-market engineering by solving material problems to develop and improve medical devices and manufacturing processes and advance the strategic goals of the company. | 11/11/2024 |
| 2189 | CooperSurgical Tucson, AZ Technician I - Stem Cell Processing Tissue Bachelors in Laboratory Science Exp: 1 year |
Process cord blood and cord tissue samples at all workstations trained and maintain certifications. Adhere to guidelines set forth by the CBR Safety Program, understand job hazard analysis concerns, and communicate safety issues to the applicable Safety Representative. Communicate deviations from procedures, anomalies, and abnormalities to responsible parties (Supervisor, Management, Department, etc.). Perform all assigned duties in compliance with internal policies, processes and Standard Operating Procedures (SOPs) as well as external regulations as determined by regulatory agencies. Responsible for remaining current in all training. Perform repetitive tasks while maintaining attention to detail. Audit, verify, and maintain accurate records for each sample. Maintain donor, client, and employee confidentiality. Evaluate disposables and equipment for non-conformities and notify responsible parties (QC, Supervisor, and/or Management). Perform daily department startup /shutdown checklist tasks and documentation. Perform general lab cleaning and maintenance. Participate in department projects as needed. | 11/11/2024 |
| 2190 | CooperSurgical Portland, OR Laboratory Technician I Bachelor's degree in Science Exp: 1-2 years |
Maintains demonstrated proficiency with all applicable Standard Operating Procedures. Performs semen evaluations to screen, process, and preserve for future clinical use. Execute an array of laboratory procedures. | 11/11/2024 |
| 2191 | CooperSurgical Boston, MA Laboratory Technician I Bachelor's degree in Science Exp: 1-2 years |
Maintains demonstrated proficiency with all applicable Standard Operating Procedures. Performs semen evaluations to screen, process, and preserve for future clinical use. Execute an array of laboratory procedures. | 11/11/2024 |
| 2192 | CooperSurgical Livingston, NJ Laboratory Technician I Bachelor’s or Master’s Degree in Biology or other related science Exp: 1 year |
Performs complex molecular-based procedures on clinical samples with a high degree of quality and in accordance with standard operating procedures. Analyzes clinical results and provides diagnoses. Communicates and collaborates with other professionals within the company and clients, as needed. Properly uses and maintains laboratory equipment. Performs clerical tasks associated with clinical cases, including but not limited to: maintenance of specimen and case logs, preparation/documentation of assay worksheets, preparation of analysis sheets and clinical reports. Receives and verifies clinical samples. Witnesses hands-on clinical procedures. Participates in lab maintenance (i.e. cleaning, annual/bi-annual/monthly maintenance of equipment, unpack supplies, etc.). Complies with Safety Standards and Good Lab Practices. Performs additional duties or assignments as directed by management | 11/11/2024 |
| 2193 | CooperSurgical Tucson, AZ Technician II - Stem Cell Processing Tissue Bachelors in Laboratory Science Exp: 1 year |
Process cord blood and cord tissue samples at all workstations trained and maintain certifications. Adhere to guidelines set forth by the CBR Safety Program, understand job hazard analysis concerns, and communicate safety issues to the applicable Safety Representative. Communicate deviations from procedures, anomalies, and abnormalities to responsible parties (Supervisor, Management, Department, etc.). Perform all assigned duties in compliance with internal policies, processes and Standard Operating Procedures (SOPs) as well as external regulations as determined by regulatory agencies. Responsible for remaining current in all training. Perform repetitive tasks while maintaining attention to detail. Audit, verify, and maintain accurate records for each sample. Maintain donor, client, and employee confidentiality. Evaluate disposables and equipment for non-conformities and notify responsible parties (QC, Supervisor, and/or Management). Perform daily department startup /shutdown checklist tasks and documentation. Perform general lab cleaning and maintenance. Participate in department projects as needed. | 11/11/2024 |
| 2194 | CooperSurgical Cambridge, MA Laboratory Technician I Bachelor's degree in Science Exp: 1-2 years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 11/11/2024 |
| 2195 | CooperSurgical Los Angeles, CA Laboratory Technician 1 Bachelor's degree in Science Exp: 1-2 years |
Maintains demonstrated proficiency with all applicable Standard Operating Procedures. Performs semen evaluations to screen, process, and preserve for future clinical use. Execute an array of laboratory procedures. | 11/11/2024 |
| 2196 | Corcept Redwood City, CA Clinical Trial Assistant I BA/BS Exp: 0-5 years |
The Clinical Trial Assistant will assist the study team in ensuring the most effective and efficient conduct of clinical research projects by providing planning, implementation, and tracking support. | 11/11/2024 |
| 2197 | Corden Pharma Boulder, CO QC Analyst - Days Bachelor's Degree (BA) Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 11/11/2024 |
| 2198 | Corden Pharma Boulder, CO QC Analyst - Nights Bachelor's Degree (BA) Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 11/11/2024 |
| 2199 | Cresilon Brooklyn, NY Production Technician I, 2nd Shift Bachelors Degree Exp: 0+ years |
The Production Technician I is responsible for the aseptic manufacturing of Cresilon’s products for the animal health industry. The Production Technician II will be trained in clean room operations, aseptic techniques, and must demonstrate the ability to successfully pass gowning qualifications. The position involves operating simple and complex processing equipment, routine sanitization of cleanroom facilities, and manual cleaning of equipment. The ideal candidate will have a proven track record of steady progress in a similar manufacturing environment and must possess a willingness to learn all equipment and jobs in the assigned manufacturing and sanitation of clean room facilities as required. Production Technicians are also responsible for the quality of products produced by ensuring compliance with local, State and Federal regulations, including current Good Manufacturing Practices (cGMP). | 11/11/2024 |
| 2200 | Crystal Pharmatech Cranbury, NJ Associate Research Scientist / Research Scientist – Solid State and Pre-formulation B.Sc. or M. Sc. degree in Chemistry, Pharmaceutical Science, or related field. Exp: 1 year |
The Associate Research Scientist will report directly to a Senior Research Scientist and handle all areas of solid-state research applied to API and early formulation development. This includes crystal form screening, single crystal growth, early formulation development, and all aspects of physicochemical characterization. The candidate will develop experimental designs and must actively communicate across multiple functional areas. | 11/11/2024 |
| 2201 | CSBio Menlo Park, CA Chemist, Quality Control Bachelor’s in chemical engineering or chemistry Exp: 1 year |
CSBio is a peptide contract manufacturing founded in 1993. Our initial products were a complete line of automated synthesizers for manufacturing and process development, with a focus on cGMP production. In 1994, we opened our custom peptide facility and began producing high quality compounds for research organizations and pharmaceutical companies worldwide. In 2004, we opened our peptide production facility in Menlo Park, CA and in 2014, we expanded our production capability through the addition of a new, state of the art building dedicated to cGMP peptide production. In 2017, we passed a FDA inspection and were recommended to be approved for commercial drug substance manufacturing. In 2023, we added additional cGMP clinical production capacity in Milpitas, CA. | 11/11/2024 |
| 2202 | CSL Miami, FL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 11/11/2024 |
| 2203 | CSL Kankakee, IL Senior Automation Engineer, Process Recipe Owner Bachelor of Science in an Engineering or other Science discipline Exp: 1 year |
Primarily accountable for the implementation, life-cycle management, and ownership of process recipes. These recipes and associated S-88 based library objects leverage a batch manager for execution and integration to MES functions. This single recipe design philosophy is referred to as Recipe Driven Execution (RDE). | 11/11/2024 |
| 2204 | CSL Springfield, IL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 11/11/2024 |
| 2205 | Curia Rensselaer, NY Quality Assurance Specialist I Bachelor’s degree in Life Science or related field Exp: 0-3 years |
The Quality Assurance (QA) Specialist I is responsible for maintaining Quality databases and providing an on-the-floor QA presence and oversight to manufacturing operations. This position’s role will include identifying compliance risks in the operation prior to and during execution, avoiding deviation whenever possible as well as managing immediate corrective action such that a) adherence to cGMPs and internal procedures/policies are maintained, and b) appropriate immediate corrective action is implemented and effectively documented in order to provide traceability and substantiation of any claims to be made in the investigation. This position primarily works in the cGMP production areas to manage adherence to the quality system and to initiate and assist in the initiation and resolution of deviations. | 11/11/2024 |
| 2206 | Curium Maryland Heights, MO Quality Control Technician Bachelor Degree in life science or a related field Exp: 1+ years |
Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP's and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management/Supervision that presents potential negative impact to manufactured or marketed product. | 11/11/2024 |
| 2207 | Perceptive New Haven, CT Chemistry Lab Technologist M.S. or B.S in a related field Exp: 1-3 years |
The role is responsible for the manufacturing of radiopharmaceuticals, conducting analytical techniques to evaluate made products and providing support to other teams within the Clinical Chemistry department. | 11/04/2024 |
| 2208 | Perceptive Needham, MA Laboratory Technician B.S. or B.A. in scientific discipline Exp: 1 year |
This position will have primary responsibility for maintaining lab cleanliness; assisting with managing hazardous and non-hazardous waste streams; receiving, distributing, and notifying other lab staff of incoming shipments. Additionally, this position may support Facilities and Lab Management staff with light equipment and facility maintenance, maintaining consumable supply inventory, and assist in managing our lab/office recycling. Other clerical and project support duties may be assigned as well. | 11/04/2024 |
| 2209 | Cambrex Longmont, CO Scientist I/II (Materials Characterization) BS Degree or MS Degree in Chemistry or related discipline Exp: 1-5 years |
As a Scientist within our Materials Characterization department, you will execute analytical methods and provide general analytical support, such as release and stability testing of drug substances and drug products. | 11/04/2024 |
| 2210 | Cambrex Marlborough, MA Clean Room Analyst - Microbiological Environmental Monitoring Bachelor’s degree or higher in Microbiology or related field Exp: 1 year |
Our Clean Room Services team is looking for both entry level and veteran Environmental Monitoring Analysts that are passionate about leveraging their talents to provide an outstanding customer experience. If you’re interested in receiving excellent training and working as part of a team of experts with opportunities for growth, you’ll be a great fit in our strong company culture. As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 11/04/2024 |
| 2211 | Cambrex Charles City, IA Process Engineer I BS in Chemical Engineering Exp: 1-5 years |
The Process Engineer will be responsible for implementation of projects for the manufacture of APIs and bulk intermediates and other products from development through piloting and/or commercial production. | 11/04/2024 |
| 2212 | Biosearch Technologies Petaluma, CA Oligo Production Tech I/ II - Synthesis Bachelor’s degree in chemistry, biology, or a similar discipline Exp: 0-4 years |
The Diagnostic Oligo Production Tech I/II-Synthesis will perform tasks associated with the synthesis of RUO and diagnostic-grade oligonucleotides in a fast-paced, high-throughput manufacturing environment. To perform this job successfully, an individual must be able to satisfactorily perform each of the following essential functions. | 11/04/2024 |
| 2213 | Biosearch Technologies Petaluma, CA Oligonucleotide Production Technician - Synthesis Bachelors or Master's Degree in Life Sciences Exp: 0-2 years |
The Oligonucleotide Production Technician I – Synthesis will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide synthesis department. An Oligonucleotide Production Technician I – Synthesis can be called on to work in any production shift in the Oligo Production Department. | 11/04/2024 |
| 2214 | Biosearch Technologies Petaluma, CA Chemistry Technician I / II -Solid Support Production Bachelor’s Degree in a Physical Science Exp: 0-2 years |
This role is responsible for the manufacturing of Controlled Pored Glass (CPG) materials by following established and robust protocols. This position will primarily work with solid phase chemistry that is used in oligo manufacturing. CPG material manufacturing includes amine and nucleoside modification of native CPG at various angstrom sizes as well as modification with proprietary dyes and quenchers. The Chemistry Technician I will also be responsible for the upkeep of basic CPG equipment used in these processes. | 11/04/2024 |
| 2215 | CAMP4 Cambridge, MA Associate Scientist, Oligonucleotide Chemistry MS in chemistry or related field Exp: 1-3 years |
CAMP4 is seeking a passionate and innovative researcher to join our Chemistry team. The candidate will contribute to CAMP4’s growing in-house oligonucleotide chemistry capabilities. This is a laboratory-based role and the successful candidate will bring expertise of oligonucleotide purification and analysis to advance our antisense oligonucleotide (ASO) drugs. Reporting to a Senior Scientist, the successful candidate will be self-driven and flexible with enthusiasm for contributing in a high efficiency and fast-paced environment with the ability to adapt to changing priorities. This position will be based in our Cambridge, MA location. | 11/04/2024 |
| 2216 | Abbott Sylmar, CA Technical Services Engineer I Bachelors Degree - (Preferred Electrical Engineering, Biomedical Engineering ) Exp: 0-2+ years |
Functioning under general supervision, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and various departments through consultation. Requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. | 11/04/2024 |
| 2217 | CareDx Brisbane, CA Manufacturing & QC Associate I BA/BS in Biological or Life Sciences Exp: 0-3 years |
The Manufacturing & QC Associate I will be an integral part of the Lab Services team, responsible for producing high-quality reagents to support patient testing in our Clinical Lab. This role includes participation in routine manufacturing and process development activities and provides support in troubleshooting and process improvement efforts. The Manufacturing & QC Associate I reports directly to the Supervisor, Manufacturing & QC. This is a full-time onsite position based in our Brisbane, CA Clinical Lab. | 11/04/2024 |
| 2218 | ZEISS Remote, IA Field Support Engineer I BS degree in Electronics, Engineering, Computer Technology and related fields Exp: 0-3 years |
As a Field Support Engineer I, you get to work with an astonishing team that plays a vital role in Ophthalmic Diagnostic repair and maintenance. The Field Support Engineer I, under close supervision and direction, installs, repairs, upgrades and performs preventative maintenance on specified Carl Zeiss Meditec instrumentation in a designated field service territory. Represents Carl Zeiss Meditec at customer locations and works to achieve a high level of customer satisfaction. Maintains all company property (inventory, tools, diagnostic equipment, vehicle, etc.) in accordance with company policies. Maintains a high level of professional communication with team, customers, management, Sales and Technical Support. | 11/04/2024 |
| 2219 | ZEISS Remote, MN Field Support Engineer I BS degree in Electronics, Engineering, Computer Technology and related fields Exp: 0-3 years |
As a Field Support Engineer I, you get to work with an astonishing team that plays a vital role in Ophthalmic Diagnostic repair and maintenance. The Field Support Engineer I, under close supervision and direction, installs, repairs, upgrades and performs preventative maintenance on specified Carl Zeiss Meditec instrumentation in a designated field service territory. Represents Carl Zeiss Meditec at customer locations and works to achieve a high level of customer satisfaction. Maintains all company property (inventory, tools, diagnostic equipment, vehicle, etc.) in accordance with company policies. Maintains a high level of professional communication with team, customers, management, Sales and Technical Support. | 11/04/2024 |
| 2220 | Carlsbad Technology Carlsbad, CA Quality Assurance Assistant Bachelor’s degree Exp: Entry Level |
Perform and process in-process tests, perform other basic QA functions in raw materials, finished products and documentation when designated. | 11/04/2024 |
| 2221 | Catalent San Diego, CA Process Engineer I Master’s degree of Engineering Exp: 0+ years |
Catalent Pharma in San Diego, CA is hiring a Pharmaceutical Process Engineer I. The Pharmaceutical Process Engineer I reports to the Process Engineer Supervisor. An individual at the level of Process Engineer I will be expected to understand and execute basic setup, operation, troubleshooting, breakdown, and cleaning of designated small scale and pilot scale pharmaceutical manufacturing equipment under limited supervision. Equipment maintenance activities may include the purchasing and installation of spare parts and supplies. This individual will complete projects and demonstration batches, evaluating the formulation, equipment set points, and process procedures with supervision. Analysis of various product characteristics will be completed with minimal supervision. The Process Engineer I will participate in the technology transfer process to the manufacturing group and may participate in the batch record review process to identify risks. Other duties include supporting the manufacturing group in the GMP (Good Manufacturing Practices) suites as subject matter expert for designated projects. Other duties include the revision of SOPs (Standard Operating Procedures), as well as researching and onboarding new equipment under the direction of a senior engineer. | 11/04/2024 |
| 2222 | Catalent San Diego, CA Quality Control Chemist I Bachelor’s degree in Chemistry or Biochemistry highly preferred Exp: No exp |
Catalent Pharma in San Diego, CA is hiring a Quality Control (QC) Chemist I. The QC Chemist I will be responsible for performing various analytical techniques and common standard lab practices in order to assess the quality of pharmaceutical products under cGMPs (as applicable) and limited supervision. This position gives opportunities to broaden analytical understanding and learn the common operations in a fast-paced, early Phase-focused, dynamic Quality Control group. | 11/04/2024 |
| 2223 | Catalent San Diego, CA Process Engineer I Master’s degree of Engineering Exp: No exp |
Catalent Pharma in San Diego, CA is hiring a Pharmaceutical Process Engineer I. The Pharmaceutical Process Engineer I reports to the Process Engineer Supervisor. An individual at the level of Process Engineer I will be expected to understand and execute basic setup, operation, troubleshooting, breakdown, and cleaning of designated small scale and pilot scale pharmaceutical manufacturing equipment under limited supervision. Equipment maintenance activities may include the purchasing and installation of spare parts and supplies. This individual will complete projects and demonstration batches, evaluating the formulation, equipment set points, and process procedures with supervision. Analysis of various product characteristics will be completed with minimal supervision. The Process Engineer I will participate in the technology transfer process to the manufacturing group and may participate in the batch record review process to identify risks. Other duties include supporting the manufacturing group in the GMP (Good Manufacturing Practices) suites as subject matter expert for designated projects. Other duties include the revision of SOPs (Standard Operating Procedures), as well as researching and onboarding new equipment under the direction of a senior engineer. | 11/04/2024 |
| 2224 | Catalent San Diego, CA Associate Project Lead, Pre-Production Bachelor’s degree Exp: No exp |
Catalent Pharma Solutions is San Diego, CA is hiring an Associate Project Lead (PL) that will support pre-production teams in the management and successful delivery of assigned Projects for our Clinical Supply site. The Associate Project Lead serves as a liaison between cross functional teams to ensure project success while complying with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs). The focus will be on understanding client needs and providing excellent customer service and proactive solutions. Under direction from PL team co-ordinate projects from award stage to completion. Primary responsibilities of this position include activities related to supply chain, procurement, batch record and label creation, and other project management and coordination activities affiliated with assigned projects. | 11/04/2024 |
| 2225 | Catalent Kansas City, MO Associate Scientist II, Biologics I Analytical Chemistry Bachelor’s Degree in Life Sciences or Physical Science field Exp: No exp |
Catalent Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II, Biologics I who is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. | 11/04/2024 |
| 2226 | Catalent Madison, WI Associate Engineer – Engineering Bachelor's degree in Engineering or related scientific field Exp: 1-2 years |
The Associate Equipment Engineering candidate will work on the Equipment team within the Engineering department. The candidate will interact with Operations, Supply Chain, Process Development, Validation, Procurement, Manufacturing Science and Technology (MS&T) and Quality. | 11/04/2024 |
| 2227 | Catalent Madison, WI Process Engineer - Manufacturing Science & Technology Master’s degree in a STEM discipline Exp: 0+ years |
The Manufacturing Sciences and Technology (MS&T) department’s primary function is to serve as an agile technical services team to support process & technology transfer (e.g., mAbs, fusion proteins, enzymes, mRNA, new modalities, etc.), process readiness and execution support related to documentation, equipment, consumables and materials, and technical writing. The MS&T organization supports the Madison facility as well as the Catalent Biologic’s network through client- facing support, on-the-floor or on-call technical coverage, as well as continuous improvement and site strategy projects. The Technology Transfer groups (Upstream and Downstream) are the technical liaisons between Process Development (internal or external) and at-scale GMP manufacturing relating to process transfer. This function includes drafting and supporting required batch documentation (i.e., gap assessments, reports, batch records, product impact), as well as process modeling and facility fit including initial bill-of-material development. | 11/04/2024 |
| 2228 | MilliporeSigma San Jose, CA Process Development Scientist Master’s degree in Chemical Engineering, Pharmaceutical Sciences, Life Sciences, Chemistry, or Biochemistry Exp: 1+ years |
MilliporeSigma is looking for a Process Development Scientist to join the technical branch of the commercial organization in the greater San Francisco Bay area. The Process Development Scientist is part of a worldwide team of engineers and scientists reporting into the technical support group for MilliporeSigma’s Process Solutions business. | 11/04/2024 |
| 2229 | MilliporeSigma Miamisburg, OH Associate Quality Scientist Bachelor’s Degree in Chemistry, Biology, or other Life Science Discipline Exp: 1+ years |
Evaluate stable isotope products, raw materials and in process materials according to established procedures. | 11/04/2024 |
| 2230 | MilliporeSigma Bedford, MA Scientist - Viral Vector Applications Bachelor’s degree in Chemical Engineering, Cell Biology, or other Science discipline Exp: 1+ years |
The Viral Vector Applications Scientist at MilliporeSigma in Bedford, MA will play a pivotal role in supporting development of cutting-edge tools and technologies for the rapidly evolving cell and gene therapy market. The successful candidate will join a dynamic Applications team within Process Solutions R&D, specializing in upstream viral vector processing. This group is responsible for generating application data to address customer needs, enhance knowledge in the field, and demonstrate the performance of products and processes for Adeno-Associated Virus (AAV) manufacturing. The scientist in this strategic lab-based position will independently manage experiments, execute studies, analyze data, and effectively communicate results. Collaboration is essential, as the role requires close interaction with a diverse range of technical and non-technical stakeholders encompassing both internal teams and external partners. | 11/04/2024 |
| 2231 | Cellares South SF, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. andidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 11/04/2024 |
| 2232 | Cellipont Bioservices Woodlands, TX QA Technician II, Operations Bachelor's Degree Exp: 1-2 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician II, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician II, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician II, Operations is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks. This individual will be responsible for providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. | 11/04/2024 |
| 2233 | Cellipont Bioservices Woodlands, TX Quality Control Analyst I, Environmental Monitoring Bachelors Degree in Life Sciences Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a QC Analyst I, Environmental Monitoring (TEMP) who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QC Analyst I, Environmental Monitoring (TEMP) is responsible for Environmental Monitoring sampling, analyzing, and reporting results, and microbiological testing to support manufacturing. Works in a fast-paced environment supporting the quality control department of a CMDO for manufacturing of cell therapy drug substance, sterile finished drug product, and fill/finish. The QC Analyst I, Environmental Monitoring (TEMP) is also responsible for ensuring all personnel activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will also require the individual to demonstrate a strong ability to work cross-functionally. | 11/04/2024 |
| 2234 | Celularity Florham Park, NJ Operator, Tissue Manufacturing B.S degree in Biology, Bioengineering or related scientific discipline Exp: 1-2 years |
Celularity is seeking a dynamic individual to join a motivated team of clinical operators for the daily manufacture of multiple tissue product. Leveraging Celularity’s new, state-of-the-art cGMP capable facility, this position will make use of existing innovations and future technologies to meet and exceed manufacturing demand. | 11/04/2024 |
| 2235 | Celularity Morristown, NJ Associate Specialist, Quality Control Bachelor's degree in a scientific discipline Exp: 0-3 years |
The entry level Assoc. Specialist, QC - Temp to Perm role is responsible for supporting biobanking/ manufacturing requests. This includes the ability to interface with multiple groups, independently perform tasks, interpret results, and generate reports. | 11/04/2024 |
| 2236 | Centerline Biomedical Cleveland, OH Quality Engineer Bachelor's Degree in Engineering or related technical field Exp: 1-3+ years |
The Quality Engineer is an Exempt/Full-Time role responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 14971, ISO 13485:2016, MDSAP and FDA 21 CFR Part 820. This role supports supplier quality and monitoring primarily along with complaint/CAPA investigations, operations production and process controls, and product and service quality and the use of statistical techniques and other accepted quality principles. The Quality Engineer will also plan and execute activities concerned with the development, implementation, maintenance, and continuous improvement of Centerline’s quality systems. | 11/04/2024 |
| 2237 | Centrillion Palo Alto, CA Laboratory Technician B.A./B.S. Exp: 6 months |
We are looking for a Laboratory Technicians - multiple positions to join our R&D team in Palo Alto. The role is part of a small group that divides their focus between innovative new projects and product development. The ideal candidate will be extremely organized, familiar with basic laboratory techniques, and excited to learn and grow within the team. Technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. Candidates with knowledge and experience of PCR, library preparation, NGS sequencing or RNA seq will be given preference. | 11/04/2024 |
| 2238 | Cepheid Sunnyvale, CA Scientist II Master’s degree Exp: 0-2 years |
The Scientist II is a bench-level job focusing on real-time PCR and RT-PCR assay and product development in an FDA-QSR and ISO9001-compliant organization. The candidate will plan and execute laboratory research and demonstrate appropriate technical proficiency, scientific creativity, and collaboration with cross-functional departments. | 11/04/2024 |
| 2239 | Cepheid Sunnyvale, CA Scientist II Master’s degree in Molecular biology/Microbiology/Bioinformatics or related field Exp: 1+ years |
The Scientist II position is primarily a bench level R&D job focusing on real time PCR and RT-PCR assay and product development in an FDA-QSR and ISO9001 compliant organization. This position is part of Assay R&D and will be located in Sunnyvale, CA (Onsite). At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 11/04/2024 |
| 2240 | Cepheid Lodi, CA Manufacturing Engineer Master's degree Exp: 0+ years |
The Manufacturing Engineer II is responsible for sustaining and improving Medical Injection molding tools and processes to achieve plant manufacturing objectives for safety, quality, on-time performance, and customer satisfaction. This position will give me the opportunity to gain knowledge of using the Danaher Business Systems (DBS) tools in a manufacturing environment. This position is part of the Manufacturing Engineering Department and will be located in Lodi, CA. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 11/04/2024 |
| 2241 | Cepheid Sunnyvale, CA Senior Scientist I Master’s degree in Molecular biology/Microbiology/Bioinformatics or related field Exp: 1+ years |
The Senior Scientist I position is a bench-level job focusing on real-time PCR and RT-PCR assay verification across GeneXpert platform instruments. The candidate will plan and execute analytical studies and demonstrate appropriate technical proficiency, scientific creativity, and collaboration with cross-functional departments. May lead small studies with manageable risks and resource requirements as well as lead others to resolve project related issues. This position is part of Assay R&D and will be located in Sunnyvale, CA (Onsite). At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 11/04/2024 |
| 2242 | Cepheid Lodi, CA Process Engineer - Day Shift Bachelor’s degree Exp: 0-1+ years |
The Process Engineer supports manufacturing operations with scientific expertise to ensure successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization; failure investigation of commercialized products; support processes to ensure performance within expected parameters. Includes laboratory roles. Schedule for this role would 5am-1pm, Thursday-Monday, with Tuesday and Wednesday off. | 11/04/2024 |
| 2243 | Cepheid Lodi, CA Process Engineer- Split Shift Bachelor’s degree Exp: 0-1+ years |
The Process Engineer supports manufacturing operations with scientific expertise to ensure successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization; failure investigation of commercialized products; support processes to ensure performance within expected parameters. Includes laboratory roles. Schedule for this role will be 1pm-9pm, Monday- Friday with Saturday and Sunday. | 11/04/2024 |
| 2244 | Cepheid Lodi, CA Process Engineer- Night Shift Bachelor’s degree Exp: 0-1+ years |
The Process Engineer supports manufacturing operations with scientific expertise to ensure successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization; failure investigation of commercialized products; support processes to ensure performance within expected parameters. Includes laboratory roles. Schedule for this role will be 9pm-5am Thursday-Monday with Tuesday and Wednesday off. | 11/04/2024 |
| 2245 | Charles River Memphis, TN Biomanufacturing Technician I BS in a scientific field Exp: 0-1 years |
The BioManufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 11/04/2024 |
| 2246 | Charles River Wayne, PA Scientist 1 Biophysical 1 Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 1-3 years |
Serve as the Scientist responsible for the development and execution of moderately complex testing and characterization of biotherapeutics using biophysical instrumentation and methodologies. May be independently responsible for method feasibility, method development, method optimization, method transfers, method qualifications, method validations and routine testing under both R&D and cGMP environments. Additionally, will be responsible for management of projects including client interaction, interpretation and reporting of data of assigned research projects. | 11/04/2024 |
| 2247 | BioMérieux Durham, NC Quality Floor Support - 2nd Shift Bachelor’s Degree in Engineering, Biotechnology, Microbiology, or Biology Exp: 0 years |
The Quality Floor Support (QFS) Specialist 1 is responsible for providing quality oversight and guidance on the production floor. In this capacity, they identify and resolve exceptions in production areas and review data and records for GMP compliance. The QFS Specialist 1 routinely performs and documents walkthrough audits of bioMérieux production, warehouse and support areas. They support quality continuous improvement and investigation activities, including but not limited to customer complaints, nonconformance investigations and CAPAs. | 10/28/2024 |
| 2248 | BioMérieux Philadelphia, PA QC Engineering Technician Bachelors degree in Biology or related field Exp: 0-2 years |
Conducts activities within the Quality Control functions testing and release of finished product and any applicable in-Process audits (ensuring that manufacturing operations remain in control). This job serves as the lab technician in the QC group and entails ensuring availability of materials for QC testing, organization of lab processes and ensuring equipment is maintained / calibrated as appropriate, and departmental documentation is current and accurate. Responsible for ensuring deviations are properly documented, nonconforming material is segregated and secured, and the supporting of any projects assigned. Performs all duties using safety conscious practices. Individual must inspect/test/audit materials & processes in a timely fashion while, at the same time, ensuring conformance to all requirements | 10/28/2024 |
| 2249 | BioMérieux Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline Exp: 6 months |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and bioMérieux. A Research Associate I may receive general or detailed instruction and direct supervision on general work, new procedures, and assignments. | 10/28/2024 |
| 2250 | BioMérieux Hazelwood, MO Scientist - Tech Transfer M.S. in medical technology, biochemistry, or microbiology Exp: 1+ year |
The Industrialization department at bioMerieux is seeking a Scientist to lead transfer of drug development into manufacturing. The scientist performs process validations and provides development support which includes data review, perform experiments, and risk assessments. This individual job function would be to provide technical knowledge of manufacturing needs and support project team. | 10/28/2024 |
| 2251 | Biogen Research Triangle Park, NC Manufacturing Associate Bachelor’s Degree (STEM preferred) Exp: Recent Grad/Entry Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 10/28/2024 |
| 2252 | Biogen Research Triangle Park, NC Manufacturing Associate IV Bachelor’s Degree (STEM preferred) Exp: 6 months |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling operations, and our teams operate across the following units: Component Preparation, Compounding, Parenteral Filling/Lyophilization, Visual Inspection | 10/28/2024 |
| 2253 | Biogen Research Triangle Park, NC Engineer III, Manufacturing Sciences Anti-Sense Oligonucleotide M.S. in Biochemistry, Bioengineering, Biochemical, Chemical Engineering or related discipline Exp: 0-2 years |
The Engineer III, Manufacturing Sciences, will provide technical expertise to the clinical, PPQ, and commercial manufacturing campaigns run within the OSM facility. | 10/28/2024 |
| 2254 | BioLegend San Diego, CA Research Associate I - Antibody Applications Bachelor’s Degree in Biology, Immunology, Biochemistry, Neuroscience or other related fields Exp: 1 year |
Biolegend’s Research Associate position conducts antibody characterization and supports product development in Immunology, Oncology, Stem Cells and Neuroscience, encompassing various antibody applications including SDS-Page and Western blot, Immunoprecipitation, ELISA, flow cytometry, immunocytochemistry, immunohistochemistry, etc. This position will be responsible for effectively collecting, communicating and summarizing experimental data. | 10/28/2024 |
| 2255 | BioLegend San Diego, CA Biochemist I - ELISA BS/BA in Biology, Chemistry, or other life science related field Exp: 1+ years |
BioLegend is seeking a highly motivated Manufacturing Associate to join the Biomarker Immunoassay team in San Diego. The Manufacturing Associate will be working closely with others in the team to ensure timely manufacturing of high-quality immunoassay products under ISO13485 standards. This role will be responsible for all aspects of product manufacturing including planning/scheduling, making and testing immunoassay components and kits, troubleshooting issues associated with product quality, and documenting and reviewing production batch records to ensure accuracy and completeness. Additional responsibilities include working with the Product Development team to ensure proper transfer of new products from Product Development to Manufacturing, filling daily immunoassay kit orders from inventoried components, and making and testing custom products in a timely manner. | 10/28/2024 |
| 2256 | BioLife Solutions Bothell, WA Aseptic Technician II Bachelor’s degree Exp: 1 year |
The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 10/28/2024 |
| 2257 | Biolog Newark, DE QC Scientist Master’s degree in Life Science Exp: 1+ year |
Biolog Lab Services is seeking a detail-oriented and collaborative QC Scientist to join our growing team. In this role, you will be responsible for performing data analysis and quality control checks on all outgoing Certificates of Analysis (CofAs) and reports. We’re looking for someone who is passionate about ensuring the highest standards of accuracy, while also being a team player who is willing to support colleagues and contribute to our dynamic work environment. | 10/28/2024 |
| 2258 | Biomeme Philadelphia, PA Scientist - Biology R&D MS in Biology, Biochemistry, Biotechnology, or related laboratory science Exp: 0-2 years |
Scientists at Biomeme serve cross-functional roles, with the majority of time at the bench in support of R&D of Biomeme’s novel nucleic acid detection and extraction technologies. Scientists may be asked to work semi-independently on projects and may also interface with other groups such as Quality and Engineering in support of their efforts. | 10/28/2024 |
| 2259 | Biomere Richmond, CA In Vivo Research Associate I BS Degree in Science Exp: 1-2 years |
Research Associate works under the direct guidance of the Project Manager- Research and the general guidance of the senior staff. Research Associate is proficient in animal procedures/animal husbandry, grant, internal, and/or contract research studies according to the study protocols and to the company guidelines and standard operating procedures (SOPs). | 10/28/2024 |
| 2260 | Bionova Fremont, CA Downstream Manufacturing Associate BS in Life Sciences, or related discipline Exp: 0-1 years |
The Downstream Manufacturing Associate or Technician will actively contribute to the manufacturing and technology transfer projects at the Bionova Scientific Fremont location. As part of the Purification/Manufacturing group, you will have opportunities to work on a wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into the GMP manufacturing facility. The role will provide hands-on execution of complex experiments in a team setting. The role will support GMP readiness and manufacturing activities. The scope of responsibilities may include but are not limited to Document writing (SOPs, Equipment URSs, etc.), equipment validation execution support and single-use assembly design. | 10/28/2024 |
| 2261 | Bio-Rad Pleasanton, CA Research Associate II Bachelor's or Master’s degree in Molecular Biology, Biochemistry, Genetics, or related life science field Exp: 1-5 years |
Join Bio-Rad’s Life Science Group in developing innovative products for oncology research and biopharmaceutical testing applications. As part of an interdisciplinary team, you will contribute to the development of new products utilizing state-of-the-art droplet digital PCR (ddPCR) technology. Your responsibilities will include planning and conducting experiments, designing and optimizing ddPCR assays, analyzing and presenting data, and problem-solving. You will be involved in all stages of the product development process from proof-of-concept through launch and will help deliver applications and products that empower our customers to improve healthcare outcomes for millions. | 10/28/2024 |
| 2262 | Bio-Rad Hercules, CA Quality Engineer I Bachelor’s degree or equivalent in a related scientific discipline Exp: 0-2+ years |
The candidate will attend cross function Daily Management meetings and represent QA following up on blocking issues and implementing countermeasures. The candidate will manage the Material Review Board and ensure thorough documentation of non-conformities and risk based determination of CAPA. The candidate will review data for trends, manage corrections and corrective action and support GSC and business partners as requested. | 10/28/2024 |
| 2263 | Bio-Rad Woodinville, WA Quality Engineer I Bachelor’s degree or equivalent in a related scientific discipline Exp: 0-2+ years |
Join Bio-Rad as our Quality Engineer and work in our Woodinville, WA site! Working in this Quality Assurance role, you will attend cross functional Daily Management meetings and represent Quality Assurance to address blocking issues and implement counter measures. You will manage the Material Review Board and ensure thorough data-driven documentation of non-conformities and risk based determination of CAPA. You will review data for trends, manage corrections and corrective action and support Global Supply Chain and business partners as requested. | 10/28/2024 |
| 2264 | Bio-Rad Hercules, CA QC Specialist I - Temporary Bachelor's degree or equivalent in a life science (Chemistry, Biology) or related field Exp: 0-2 years |
A typical day will involve completion of testing on assigned batches and completing paperwork/data entry into SAP to document results for review/product release. This role requires communication and coordination between team members, the supervisor and the planners to ensure that we are keeping on top of priorities to avoid backorder. Besides routine testing, a day will include attending the daily Tier 1 meetings to report on safety, quality, delivery and inventory updates. | 10/28/2024 |
| 2265 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline Exp: 1-6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 10/28/2024 |
| 2266 | Bio-Techne Minneapolis, MN Advanced Research Associate Master's degree in chemistry, biological sciences, or equivalent (chemistry or biochemistry preferred) Exp: 0-2 years |
As an Advanced Research Associate in the Conjugation lab, you will be responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, you may help prepare and test other chemistry related reagents for manufacturing and QC teams. This is a fantastic opportunity for you to grow your analysis, problem solving, and troubleshooting experience in a collaborative and energetic biotech manufacturing environment. You will find that this position offers continuous learning and development as you grow your product knowledge, technical manufacturing & testing expertise, and engage in a variety of lab techniques every day. | 10/28/2024 |
| 2267 | Bio-Techne Minneapolis, MN Quality Technician Bachelor’s degree in Biology, or related field of study Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. Other tasks include proofing labels and assay sheets. This position will adhere to safety regulations. Perform additional duties as assigned. | 10/28/2024 |
| 2268 | Bio-Techne San Marcos, CA QC Specialist Bachelor’s degree in Biological Science, Chemistry, or related field Exp: 1-5 years |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. | 10/28/2024 |
| 2269 | Bio-Techne Minneapolis, MN Research Associate Bachelor’s degree in biochemistry, microbiology, biotechnology,?or equivalent Exp: 0-2 years |
This position is responsible for the growth of E. coli in a GMP (Good Manufacturing Practice) Lab, following GMP guidelines. This includes, but is not limited to GMP, AF (Animal Free Process), and other products used by pharma and IVD customers. This position manufactures E. coli clones using shake flask, or Bioreactors using a variety of techniques, software and equipment including, Bioreactors, Shake Flasks, Biosafety cabinets, Fume Hoods, Sterile Filters, Autoclaves, and centrifuges. All procedures and batch records follow GMP guidelines. | 10/28/2024 |
| 2270 | Bio-Techne Minneapolis, MN Advanced Research Associate Master's degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday - Saturday shift. | 10/28/2024 |
| 2271 | Bio-Techne Minneapolis, MN Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday - Saturday shift. | 10/28/2024 |
| 2272 | Bio-Techne Wallingford, CT Quality Technician Bachelor of Science degree in relevant field Exp: 0-2 years |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products. | 10/28/2024 |
| 2273 | Bora Pharmaceuticals Camden, MD Analyst l, QC Microbiology-3rd-Shift BS in Microbiology/Biology or related field. Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. This position supports our 3rd-shift, working 10pm-6:30am, Monday through Friday. | 10/28/2024 |
| 2274 | Bora Pharmaceuticals Camden, MD Analyst II, QC Microbiology-2nd Shift MS in Microbiology/Biology or related field Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Bora Pharmaceuticals Camden site to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. This position is a for our 2nd shift, working hours; 2pm-10:30pm Monday through Friday. | 10/28/2024 |
| 2275 | Bora Pharmaceuticals Camden, MD Analyst l, QC Microbiology-3rd-Shift BS in Microbiology/Biology or related field. Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. This position supports our 3rd-shift, working 10pm-6:30am, Monday through Friday. | 10/28/2024 |
| 2276 | Bora Pharmaceuticals Camden, MD Analyst I, QC Analytical B.S. in Chemistry or related field Exp: 0-2 years |
Perform analytical testing per cGMP in support of raw material, in-process, final product, stability. Typical hours are 10:00 pm – 6:30 am, Monday through Friday. Hours may vary to meet business and training needs. | 10/28/2024 |
| 2277 | Bora Pharmaceuticals Camden, MD Analyst III, Quality Assurance-Batch Release BS or MS degree in Chemistry/Biology or related discipline Exp: BS: 1-3 years; MS: 1 year |
The QA Analyst III is responsible for performing duties related to the management of records relevant to the review and release of Batch Records for the cGMP operation at Bora Pharmaceutical, the Baltimore Camden Site. Our QA Department provides expertise in problem solving and process improvements. The QA Analyst will interact with all departments to provide guidance necessary to maintain and improve cGMP compliance at the company. | 10/28/2024 |
| 2278 | BIB Southborough, MA Research Associate - Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields Exp: 0-1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision at BIB. | 10/28/2024 |
| 2279 | BostonGenes Waltham, MA Biospecimen Inventory Technician BS in a Biological or Life Science Exp: 1 year |
The candidate will report to the Lab Manager and under their supervision support BostonGenes laboratory teams with sample management and tracking systems/protocols. The candidate will create and oversee a new sample inventory tracking system using the existing Lab Information Management System (LIMS) and Benchling software. Once created they will assist in the transition to an end-to-end barcoding-based system for sample tracking and continuously update and improve the process as new tests are added. This candidate will also be responsible for handling and processing blood specimens for specific projects. This will involve basic blood processing techniques such as blood fractionation, plasma clarification, and cell isolation for downstream biobanking. | 10/28/2024 |
| 2280 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 10/28/2024 |
| 2281 | BWX Technologies Erwin, TN Engineer 1 Bachelor’s degree in Engineering, Biotechnology, Microbiology, or Biology Exp: No exp |
Responsible for routine engineering assignments applying standard engineering techniques, procedures, and criteria under guidance of a manager or experienced engineer. Assignments are designed to develop professional work knowledge and abilities. Works under close supervision. Manager screens assignments for unusual or difficult problems and selects techniques and procedures to be applied on non-routine work. | 10/28/2024 |
| 2282 | BWX Technologies Mt Vernon, IN Manufacturing Engineer Bachelor's degree in Mechanical, Manufacturing, or Civil Engineering Exp: Entry Level |
BWXT is currently seeking a Manufacturing Engineer to join our growing team in Mt. Vernon, IN! Position responsibilities include: Serve as the primary point of contact/coordinator for the program.Assist in developing detailed recovery plans for projects. Perform reviews of contract and design requirements for acceptance of quality notifications. Track status of project schedules and deliverables. Work with Unit Manager to maintain contract performance metrics. Interface with Design and Manufacturing. Engineering to manage change to component designs. Support quotes for new work by reviewing technical requirements and preparing person-hour estimates. Perform special assignments as deemed necessary. | 10/28/2024 |
| 2283 | BWX Technologies Erwin, TN Engineer 2 -- AUKUS Design Engineering -- Process MS Degree -- Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 10/28/2024 |
| 2284 | BWX Technologies Erwin, TN Engineer 2 -- AUKUS Elec & Instrumentation Eng MS Degree -- Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 10/28/2024 |
| 2285 | BWX Technologies Erwin, TN Engineer 2 -- AUKUS Design Engineering -- Mechanical MS Degree -- Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 10/28/2024 |
| 2286 | BWX Technologies Erwin, TN Nuclear Safety Eng 1 MS Degree -- Engineering Exp: 1-2 years |
Performs Nuclear Criticality Safety (NCS) activities that assure plant operations are conducted in compliance with governmental regulations and license conditions and in a manner such that a criticality excursion and its consequences will not occur. | 10/28/2024 |
| 2287 | ATEC Carlsbad, CA Systems Engineer I BS Degree in Engineering Exp: 0-2 years |
The Systems Engineer will be a key participant in many steps along the product development pathway, including system requirements development and documentation, development testing, design verification testing, Design History File compilation, validation and iterative improvement processes. | 10/22/2024 |
| 2288 | AustinPx Georgetown, TX Process Engineer I Bachelor’s Degree in Engineering, Chemical Engineering Exp: 0-2 years |
Work within a cGMP quality system, including participating in manufacturing activities under limited supervision. Complete process development and scale up activities in collaboration with formulation development and manufacturing to enable clinical trial material manufacturing. Prepare master batch records (MBRs). Utilize statistical design of experiment and process control schemes to optimize outcomes. Solve technical issues relating to the manufacture of dose form/product using process analysis tools. Design Experiments to investigate the relationships between material attributes, process parameter/equipment selection, and product quality. Generate process development/optimization protocols and reports. Assist with all necessary activities to procure and install equipment, including developing requirements, setting up, qualification protocol writing & execution, SOP development. Scale up of manufacturing processes from pilot to commercial scale. Participate in process technical transfer of manufacturing processing to 3rd party Contract Development and Manufacturing Organizations (CDMOs) to enable commercial manufacturing. Travel to CDMOs to oversee process transfer and manufacturing. Develop a strong understanding of specific equipment utilized internally and at CDMOs. | 10/22/2024 |
| 2289 | Avance Biosciences Houston, TX Lab Associate II BS in Biochemistry, Molecular Biology, or related field Exp: 1+ years |
Perform analytical experiments following company SOPs and instructions from superiors. Maintain good documentation and assist in problem solving. Strictly following FDA regulations (GLP and CGMP) while executing experiments | 10/22/2024 |
| 2290 | Avantor Sciences Irving, TX Project Engineer 1 Bachelor’s degree in Mechanical, Electrical, or Chemical Engineering Exp: 1-3 years |
Works independently under close supervision, responsible for the engineering and technical disciplines needed to complete a project. Plan projects, establish project criteria, coordinate project reviews, and ensure the proper implementation of project elements. Formulate project parameters and assigning responsibilities to the most capable employees and monitoring the project team. Create frameworks to measure the project's metrics and data collection. | 10/22/2024 |
| 2291 | Avantor Sciences Bridgewater, NJ Associate Scientist - Upstream (mRNA) BS (biochemistry, molecular biology, cell biology, chemical engineering, bioengineering or related). Exp: 1+ year |
The successful Associate Scientist - Upstream (mRNA) candidate will bring an eagerness to learn, strive for highly productivity, be well-organized and self-motivated. This high potential role will be responsible for the hands-on execution of cell culture laboratory experiments for the process development and basic analytical studies. The hired candidate will make detailed observations, analyze data, interpret results, and exercise appropriate technical judgment in the execution of studies. | 10/22/2024 |
| 2292 | Avid Bioservices Tustin, CA Manufacturing Associate, Downstream Bachelor’s with a preference for Biology or Chemistry emphasis. Exp: 1-2+ years |
Join our dynamic team as a Manufacturing Associate, Downstream! In this role, you'll be a crucial part of our multi-product manufacturing facility, working in strict compliance with cGMP and Standard Operating Procedures. Your responsibilities will encompass various tasks, including production, meticulous documentation, report writing, materials procurement, and equipment scheduling. You'll be instrumental in ensuring the timely production and release of top-quality products. At our company, we value core principles such as Integrity, Adaptability, Innovation, Teamwork, and Passion, all united by a shared mission to enhance patients' lives through the consistent delivery of high-quality biopharmaceuticals. If you're ready to make a meaningful impact, apply now and be part of our journey! | 10/22/2024 |
| 2293 | AXIS Dilworth, MN Analytical Chemist I Bachelor’s degree in Biology, Chemistry, or equivalent. Exp: 1 year |
The Analytical Chemist I, Bioanalytical Operations carries out various Bioanalytical functions of the organization. The Analytical Chemist is responsible for executing Bioanalytical methods within AXIS Clinicals. | 10/22/2024 |
| 2294 | AxisPharm San Diego, CA Lab Technician Bachelor’s degree Exp: 0-4 years |
Maintain inventory accuracy and erform database reconciliation on daily basis. Familiarity with automated laboratory equipment, scientific database, E-notebook a plus. Assist with laboratory support tasks such as documentation management, shipping/receiving. Adheres to laboratory safety standard, including proper use of PPE, safety enclosures and other equipment. | 10/22/2024 |
| 2295 | BA Sciences Morrisville, NC QA Specialist I Bachelor’s degree in a related science discipline Exp: 0-3 years |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing analytical data, routine work, protocols and reports. | 10/22/2024 |
| 2296 | BA Sciences Salem, NH Analytical Chemist I, RM Bachelor’s degree in Chemistry or a related discipline Exp: 0-3 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties include performing analysis of Raw Materials using AA, UV-Vis, and Wet Chemical Analysis according to USP/EP methods. | 10/22/2024 |
| 2297 | BA Sciences Salem, NH Microbiologist I - Microbiome BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/22/2024 |
| 2298 | BA Sciences Salem, NH Microbiologist I, QC BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/22/2024 |
| 2299 | BA Sciences Salem, NH Microbiologist II, Microbiome BA or BS degree in Microbiology or related science discipline Exp: 1-5 years |
The Microbiologist II conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/22/2024 |
| 2300 | Bachem Vista, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 10/22/2024 |
| 2301 | Baxter Saint Paul, MN Sterility Associate I BS Degree in Science, Engineering or Math or other relevant field Exp: 1+ year |
As the site Sterility Associate, you will serve as the primary resource for the team and support development, validation and maintenance of sterilization processes and cleanroom certification. This position plays a substantial role in the qualification and/or validation of sterilization, cleanroom, equipment, raw materials, and manufacturing processes. In this role you will directly impact the health and safety of our end-users, our patients. | 10/22/2024 |
| 2302 | Baxter Hayward, CA Analyst I, Quality Control Lab Bachelor’s degree in Chemistry or Biological Sciences with Analytical Chemistry Exp: 0-2 years |
Conduct specific chemical and physical analysis on medical devices through all stages of the manufacturing process from incoming raw materials to finished goods. Responsible for overall sample and materials management activities supporting the QC laboratory. | 10/22/2024 |
| 2303 | Baxter Medina, NY Manufacturing Engineer Bachelor’s degree in engineering (Biomedical, Mechanical, Industrial, Electrical or Chemical Engineering) Exp: 1-3 years |
This description outlines the employment prerequisites and job responsibilities for the position of Manufacturing Engineer within the Continuous Improvement Team. Provide support in the execution of the site’s operational optimization and quality improvement projects to achieve Medina Plant goals and objectives. Drive/support various quality improvement, business continuity/expansion, and cost reduction initiatives from identification through implementation while working with cross functional resources to ensure results are achieved in a timely manner. | 10/22/2024 |
| 2304 | Baxter Round Lake, IL Quality Lab Associate I Bachelors degree in Chemistry or Science related degree Exp: 6+ months |
The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. **This is a first shift position that will be required to work on Saturday to Tuesday to support training of analysts and to support projects and/or production, as required.** A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 10/22/2024 |
| 2305 | Baxter Cleveland, MS Process Engineer - Injection Molding Bachelor's Degree in Engineering Required (Mechanical, Industrial, Electrical, Chemical, or Polymer Science degrees are preferred) Exp: 0-2 years |
This position is a key role in the Injection Molding Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Injection Molding Operations. You will also be involved in Multi-functional project management within this role. | 10/22/2024 |
| 2306 | Baxter Cleveland, MS Process Engineer - Bottled Solutions Bachelor's degree in engineering required. (Mechanical, Industrial, Electrical, or Computer degrees are preferred) Exp: 0-2 years |
This position is a key role in the Bottled Solutions Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Bottled Solutions Operations. Multi-functional project management will be involved in this role as well. | 10/22/2024 |
| 2307 | Baxter Mountain Home, AR Quality Lab Associate Bachelor of Science in Chemistry Exp: 0-2 years |
Responsible for the outgoing quality, safety, and efficacy of product produced at Mountain Home (relative to Chemistry Laboratory analyses) involving complex routine and non-routine testing and validation in the Chem Lab. | 10/22/2024 |
| 2308 | Inotiv Rockville, MD Quality Assurance Auditor I B.S. in chemistry or life sciences or B.S./B.A. in related field Exp: 1-3 years |
Interact with clients, other employees, and the community in a professional manner. Support and participate in company initiatives as directed. Maintain thorough knowledge of facility SOPs, policies, study protocols, etc. Adhere to all safety regulations and procedures. Provide assistance or support to other Inotiv QA team members as necessary. Perform other duties as assigned. | 10/22/2024 |
| 2309 | Inotiv Raleigh, NC Associate Scientist Bachelors Degree biology or related field Exp: 0-1+ years |
Conduct GLP and non-GLP genetic toxicology assays (i.e. Ames, Comet, and micronucleus assays). Maintain and dose cultured cells, including primary cells and stem cells. Perform laboratory maintenance tasks (e.g. material storage and disposal, equipment monitoring/maintenance, etc.). Assist in the maintenance of supply inventories. Maintain study books. Handle data (e.g. organize data, prepare data tables). Train others in basic lab skills. Perform peer reviews of laboratory records and study documentation. Participate in the Quality Assurance audit process. | 10/22/2024 |
| 2310 | Inotiv Raleigh, NC Associate Scientist Bachelors Degree biology or related field Exp: 0-1+ years |
Conduct GLP and non-GLP genetic toxicology assays (i.e. Ames, Comet, and micronucleus assays). Maintain and dose cultured cells, including primary cells and stem cells. Perform laboratory maintenance tasks (e.g. material storage and disposal, equipment monitoring/maintenance, etc.). Assist in the maintenance of supply inventories. Maintain study books. Handle data (e.g. organize data, prepare data tables). Train others in basic lab skills. Perform peer reviews of laboratory records and study documentation. Participate in the Quality Assurance audit process. | 10/22/2024 |
| 2311 | Bausch + Lomb Rochester, NY Scientist I, R&D Microbiology B.S. or M.S. Exp: 0-3 years |
Monitoring product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 10/22/2024 |
| 2312 | Beckman Coulter Diagnostics Chaska, MN Manufacturing Controls Engineer II Master's degree in engineering Exp: 0+ years |
The Manufacturing Engineer II for Beckman Coulter Diagnostics is responsible for supporting our reagent operations equipment, assessing equipment for optimization, qualifying replacements, monitoring our processes and driving to exceed our customer’s demands to ensure our patients have the tests they need. This position is part of the Reagent Operations located in Chaska and is on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Engineering team and report to the Process Engineering Manager responsible for the design, implementation and support of manufacturing processes, and equipment. If you thrive in a fast-paced role and want to work to build a world-class manufacturing organization. | 10/22/2024 |
| 2313 | Beckman Coulter Diagnostics Miami, FL System Integration Engineer Master’s degree in a related Engineering discipline (Electrical Engineering, Mechanical, Biomedical, Systems Engineering) Exp: 0+ years |
The Systems Integration Engineer for Beckman Coulter Diagnostics will be a critical team member working cross-functionally on programs developing new products, and in supporting legacy instrumentation in cost reduction, product design changes due to regulatory and environmental standard revisions, and customer driven product enhancements. This position is located in Miami, FL with the Hematology/Urinalysis Business Unit, and is on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will work within the Systems Engineering team and report to the Senior Manager of Systems and Hardware, New Product Development responsible for leading design tasks that create novel hardware, fluidics and electronics, and for integrating these systems, along with reagents and algorithms, into world-class clinical diagnostics analyzers. If you thrive in an amazing, innovation-oriented, challenging role and want to work to build an amazing systems engineering and test organization. | 10/22/2024 |
| 2314 | Beckman Coulter Diagnostics Miami, FL Systems Engineer II Master's degree in Engineering (ME, EE, Biomedical Engineer, Chemical Engineering or related technical subject area) Exp: 0+ years |
As a member of the R&D Hardware team, this role will report to the Manager, Systems Engineering responsible for development and sustaining of in vitro diagnostic products. If you thrive in a dynamic role and want to join an extraordinary R&D organization. | 10/22/2024 |
| 2315 | Beckman Coulter Diagnostics Carlsbad, CA Technician Production Operations Bachelor’s degree Exp: 0-1+ years |
The Reagent Formulations Technician for Beckman Coulter Diagnostics is part of a formulation team responsible for the manufacturing of reagents used in the medical diagnostics field. This role is critical to the healthcare industry and to allow doctors and lab technicians to diagnose patients quickly and accurately all over the world. This fully onsite position reports to the Supervisor for Aqueous Formulations and is part of the Production Operations Department located in Carlsbad, CA. If you thrive in a fast paced, detail-oriented role and want to work to build a world-class, quality focused manufacturing organization—read on. | 10/22/2024 |
| 2316 | Beckman Coulter Diagnostics Chaska, MN Quality Assurance Scientist I Bachelor´s degree in Science or Engineering related discipline Exp: 0-2 years |
The Quality Assurance Scientist I for Beckman Coulter Diagnostics is responsible for investigating customer complaints for the Immunoassay product line. This position is part of the Complaint Handling Unit located in Chaska, Minnesota and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Post Market Surveillance organization and report to the Post Market Quality Assurance Manager responsible for ensuring complaints are correctly classified, records are populated per the current procedures and policies, and are investigated in a timely manner. If you thrive in a multifunctional role and want to work to build a world-class post market surveillance organization. | 10/22/2024 |
| 2317 | BD Zelienople, PA Manufacturing Quality Engineer B.S. or B.A. Degree in Science-related field, Quality Assurance, Engineering, Mathematics/Statistics or equivalent. Exp: 1 year |
The Quality Engineer performs various quality-engineering functions and associated support tasks in developing knowledge and experience in the areas of Quality Assurance. The role provides guidance for the various elements of the Quality System, for example, to ensure process control and identifies/recommends opportunities for continuous improvement (internal/external). Applies the appropriate statistical tools to analyze data, identify root cause and corrective actions for effective problem resolution of small to moderate in scope and complexity. May support both internal and external audits. | 10/22/2024 |
| 2318 | BD Mebane, NC Associate Quality Scientist Bachelor’s degree in Biology, Microbiology or other related Life Science Exp: 1-2 years |
Reporting to the Quality Scientist/Lab Supervisor, the BD Mebane Associate Quality Scientist is responsible for applying basic scientific principles to routine laboratory work, executing product testing, applying/interpreting scientific data of moderate complexity, ensuring good laboratory practices, and processing data generated from Quality Control testing. | 10/22/2024 |
| 2319 | BD Warwick, RI Product Development Engineer 1 Bachelor's degree in engineering or other applicable science field Exp: 1 year |
Direct project responsibility for design, development of new and improved products. Performance against schedule affects commitments made in the division business plan. Recommends product specifications, drawings, documents and changes as they pertain to any new products or product modifications. | 10/22/2024 |
| 2320 | Bend BioScience Bend, OR Analytical + Materials Scientist BS/BA in chemistry, pharmaceuticals, or related field Exp: 1-3 years |
Analytical and materials scientists will be responsible to progress programs collaboratively with multi-disciplinary teams by: Designing experiments tailored at challenging formulation attributes critical to successful formulation strategies. Performing materials characterization using expertise in analytical characterization to inform physical, chemical, and performance attributes for a range of formulation compositions. Running typical pharmaceutical analytical and materials science techniques for characterization (HPLC, GC, FT-IR, HPLC/UV, DSC, SEM, XRD). Efficiently interpreting results with a broad understanding of impact to formulation performance and robustness. Understanding and applying basic concepts of HPLC method development in support of early formulation work. Staying aware and current with pharmaceutical industry best practices in analytical chemistry. Demonstrating problem solving and troubleshooting ability related to routine procedures. Independently reviewing and interpreting complex analytical methods in support of formulation screening activities and implementing them in the lab in a timely manner. Independently documenting lab work in protocol, reports, and other required documentation. Ensuring preparation and timely delivery of data in support of formulation and manufacturing projects. | 10/22/2024 |
| 2321 | Bend BioScience Bend, OR Analytical scientist BS/BA in chemistry, pharmaceuticals, or related field Exp: 1-2 years |
Analytical scientists will be responsible to progress programs collaboratively with multi-disciplinary teams by: Analytical method development to support release of pharmaceutical intermediates and finished oral dosage forms including: HPLC, GC, FT-IR, PXRD, KF, and particle size. Understanding and applying basic concepts of HPLC method development in support of early formulation work Running typical pharmaceutical analytical techniques for characterization (HPLC, GC, FT-IR, KF, DSC, SEM, XRD, Particle Size). Demonstrating problem solving and troubleshooting ability related to routine procedures. Independently reviewing and interpreting analytical methods and implementing them in the lab in a timely manner. Independently documenting lab work in protocol, reports, and other required documentation. Ensuring preparation and timely delivery of data in support of formulation and manufacturing projects. | 10/22/2024 |
| 2322 | Bifrost Biosystems Berkeley, CA Mechanical Engineer BS or MS in Mechanical Engineering or a related field. Exp: 0-4 years |
Are you passionate about pushing the limits of technology to advance our understanding of the life sciences? So are we! We’re looking for a highly motivated and experienced Mechanical Engineer to join a fast-paced start-up developing tools that will transform functional cell biology research. The ideal candidate will have strong engineering and problem-solving skills, a solid grasp of mechanical design fundamentals and some exposure to optical systems, microscopy and bio-engineering or biology. As Mechanical Engineer, you will be part of a small team designing, developing, specifying and testing Bifrost’s hardware products. Additionally, you will play a role in product definition, development and verification testing. | 10/22/2024 |
| 2323 | Biocytogen Boston, MA Pharmacology Research Associate Bachelor’s or Master’s degree Exp: 1-3 years |
Biocytogen is a comprehensive research and discovery service provider for biotech and pharmaceutical industry and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, and animal supplies, with the current focus on immuno-oncology and oncology. We are looking for a highly motivated research associate with the ability to work both independently and collaboratively. Biocytogen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Biocytogen is committed to nurturing junior scientists to progress within our organization, providing a supportive environment for career advancement. This opportunity is ideal for individuals who can recognize and seize learning opportunities. | 10/22/2024 |
| 2324 | BioEclipse Therapeutics Mountain View, CA Research Associate/Scientist BA, BS, or MS in Biology related field (Immunology, Virology, Hematology, Cell Biology, Microbiology, Molecular Biology, Biochemistry, etc.) Exp: 1-5 years |
Our R&D team is seeking a motivated Research Associate/Scientist to develop and perform assays central to the advancement of our novel immune therapeutic and to assist in the development of our platform. The person we are looking for is well organized, has good communication skills, and can work both independently and in multi-disciplinary teams. We are seeking candidates with experience working with pathogens, specifically viruses, who are proficient in cell culture, and ideally have GMP or process development experience. We are seeking candidates with hands-on laboratory experience such as cytotoxicity assays, quantitative PCR, flow cytometry, immunohistochemistry, and cell and virus harvesting. | 10/22/2024 |
| 2325 | Biofidelity Morrisville, NC Molecular Technologist II (2nd shift) Master’s degree in medical laboratory science or biological or chemical sciences Exp: 1+ years |
Biofidelity is seeking a Molecular Technologist II to perform high complexity diagnostic testing using Biofidelity’s ASPYRE technology, histology, and nucleic acid extraction workflows. With minimal oversight from the Supervisor, the Molecular Technologist II will be responsible for the efficient and quality execution of sample accessioning, processing, data generation, and reporting in the clinical laboratory. The ideal candidate has strong molecular biology technical skills, is collaborative, trustworthy with ability to work in a fast-paced clinical environment. This role reports to the Molecular Tech III, Team Lead. | 10/22/2024 |
| 2326 | BioMérieux Hazelwood, Mo Final QC Technical Lab Lead Bachelor’s Degree in Biology, or other equivalent discipline Exp: 0 years |
Provide direction to the Lab team including communicating lot status and priorities to the group and demonstrating good aseptic lab practices. Prioritize lab tasks to ensure the schedule is met. Assists and trains others as needed in performing and documenting testing. In addition, the position is responsible for ensuring proper documentation according to cGMP’s and current procedures. Using good aseptic lab practices, it supports performance testing and physical inspections of finished good lots and internal use only lots through set up of VITEK2 cards, to completion. | 10/22/2024 |
| 2327 | AstraZeneca Frederick, MD Quality Control Analyst (Sun-Wed) Bachelor’s degree in scientific/ biotech/ pharmaceutical or relevant field of study Exp: 0-3 years |
Join our Operations team as a Quality Control Analyst, where will be responsible for performing laboratory testing. This is an exciting opportunity to accelerate our Lean journey and take advantage of the huge opportunities to drive efficiencies in our processes and produce better-quality outputs. As a Quality Control Analyst, you will perform selected quality control testing activities, including raw materials, in process, finished product, and stability testing according to standard operating procedures. You will be responsible for conducting troubleshooting equipment problems, entering data evaluated for compliance to specifications, and reporting abnormalities. You will also be involved in writing new standard operating procedures or revising existing documentation. Your role will require you to apply critical thought to solving problems and work on problems requiring an in-depth knowledge of scientific methods and techniques. | 10/15/2024 |
| 2328 | AstraZeneca Santa Monica, CA Research Associate, Process Development MS degree in Immunology, Cell Biology, Molecular biology, Bioengineering, or relevant degrees Exp: 6 months |
As a Research Associate, you will manage process development studies to develop, optimize, scale-up and transfer cGMP manufacturing processes. You will carry out flow cytometry and cell-based assay experiments for the characterization of and optimization of cell therapy manufacturing processes. You will also perform cell culture of T cells in multiple formats including flasks, bags, and bioreactors. Collaborating within the project team to interpret study results and contribute to technical discussions for subsequent study design is also part of your role. You will prepare and review experimental proposals, technical reports, SOPs and manufacturing batch records. Working collaboratively within PD group and cross-functionally with other groups to meet Technical Operation organization goals is essential. | 10/15/2024 |
| 2329 | AstraZeneca Santa Monica, CA Associate, Quality Control Analytical Master's degree in Biological Sciences or related field Exp: 1 year |
We are looking for an energetic and experienced person with cell therapy quality control background to join our Quality Control (QC) team. You will contribute to the advancement of our product pipeline by performing QC analytical method qualification, complete sample analysis, and other assigned tasks. You will also independently organize and present results and conclusions. You will ensure that the QC Analytical laboratory is operating as expected. | 10/15/2024 |
| 2330 | AstraZeneca Mount Vernon, IN Validation Engineer Bachelor’s degree in Engineering, Chemistry, Biology, or Pharmaceutical Sciences Exp: 0-3 years |
As a Validation Engineer, you will perform installation and operational and performance qualification (IQ/OQ/PQ) of critical manufacturing equipment, facilities, and utility systems. Your responsibilities will include developing and reviewing qualification protocols and reports, coordinating system and equipment documentation collection, and executing protocols. You will also solve qualification and cleaning validation execution issues using critical analysis skills and develop sound, reasoned solutions and recommendations. | 10/15/2024 |
| 2331 | AstraZeneca Waltham, MA Scientists, ADC/RC Target Biology Masters degree experience in Biology, Oncology, Biochemistry, Pharmacology, Molecular Biology, Cell Biology, or a related field. Exp: 1+ years |
We are currently seeking a highly motivated Scientist (non-PhD) with strong scientific excellence and technical expertise in oncology research to join our ADC Biology and Development team at Waltham, MA USA, within the Oncology Targeted Discovery (OTD) group. | 10/15/2024 |
| 2332 | AstraZeneca Gaithersburg, MA Associate Scientist, Late-Stage Formulation Sciences BS in Chemistry, Biochemistry, Pharmaceutical Sciences, Bioengineering or a related field Exp: 0-2+ years |
The Late-Stage Formulation Sciences (LSFS) Group is responsible for development of intended commercial formulations to advance AstraZeneca’s late stage biologics portfolio, and the life cycle management of commercialized products. The group plays an integral part in the design and development of patient centric drug products. As a part of Biopharmaceutical Development, the Late-Stage Formulation Sciences group, within the department of Dosage Form Design and Development, is on a mission to develop extraordinary products through excellent science, forward-thinking execution, and compassion for patients and those who touch our products. We develop and characterize intended commercial formulations and finished dosage forms to deliver high quality biologics to the market for patients. We develop robust formulations, Drug Products, and product control strategies to ensure approval of marketing applications for product commercialization and launch. | 10/15/2024 |
| 2333 | Andelyn Biosciences Columbus, OH GMP Quality Control Scientist I (2nd Shift) BS in the life sciences, biotechnology, or gene therapy industries Exp: 0 years |
The GMP Quality Control (QC) Scientist I will perform assigned tasks to support the daily operations of the GMP QC laboratory. The primary objective is to ensure that all activities within the GMP QC laboratory facility comply with the requisite regulations (21 CFR Part 211 Subpart I, 21 CFR Part 11, et. al.). Working in close collaboration with QC Management, and senior QC staff the Scientist I will aid all day-to-day lab operations, including project and timeline management, materials management, assisting with laboratory investigations, SOP generation and revision, and assay performance. The Scientist I will aid QC Management in ensuring that their assigned tasks are performed by following appropriate regulatory practices, analytical methods, and Standard Operating Procedures (SOPs) for GMP. | 10/15/2024 |
| 2334 | Andelyn Biosciences Dublin, OH Scientist II Master’s in the life sciences, biotechnology or gene therapy industries preferred Exp: No exp |
A Scientist II, in Process Devlopment, will support upstream and downstream process development activities including responsibilities in bioprocessing and analytics. Working in close collaboration with PD leadership and PD scientists, scientist II will support the execution and completion of projects involving platform development, optimization, in-process characterization, and tech transfer following appropriate regulatory practices, timelines, documentation, and standard operating procedures. Prior experience in the purification of biologics is preferred. He/She will keep abreast with state-of-the-art technologies and scientific advancements in the field and participate in discussions on scale-up of processes, process qualification, and strategies for process improvement. | 10/15/2024 |
| 2335 | Andelyn Biosciences Columbus, OH Quality Assurance Specialist I BS in the life sciences, biotechnology, or gene therapy industries Exp: 0 years |
The Quality Assurance (QA) Specialist supports the manufacturing operations by performing quality assurance functions for the GMP operations. The QA Specialist will be responsible for ensuring compliance with Good Manufacturing Practices (cGMP) regulations, policies, and procedures applicable to these areas. This position will report to the Quality Assurance Manager and will work closely with the manufacturing operations staff. | 10/15/2024 |
| 2336 | AngioDynamics Marlborough, MA Regulatory Affairs Specialist - Temp Bachelors Level of Degree in a scientific or technical discipline field of study Exp: 1-2+ years |
Responsible for determining the path to market for new and modifications to existing products in compliance with Regulations of intended market territory and for guiding teams on the required deliverables to support the Regulatory status of products distributed by AngioDynamics Inc. | 10/15/2024 |
| 2337 | Anika Bedford, MA QC Microbiologist I, Environmental Monitoring Bachelors Degree preferred Exp: 1-2 years |
The QC Microbiologist I, Environmental Monitoring will learn, understand, and perform routine entry level sampling of cleanrooms and utilities according to written procedures under cGMP conditions; as well as tasks involved with clerical and logistical laboratory tasks. | 10/15/2024 |
| 2338 | Anika Bedford, MA QC Microbiologist I, Environmental Monitoring BS in microbiology, biology or related science Exp: 1+ years |
Responsible for all microbiological and some analytical testing of production materials under GMP conditions. Responsible for process and equipment validation (autoclave and depyrognenation oven) in cooperation with Engineering and R&D (New Product Sterility and LAL validation.) | 10/15/2024 |
| 2339 | Ansh Labs Webster, TX Scientist Master’s degree in Biological/Chemical Sciences/Biotechnology or related area Exp: 1 year |
As a key member of the Manufacturing or R&D Department, this individual will provide critical scientific skills to assist in the development and scale-up of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays, routine microbiology, biochemistry, and protein purification. | 10/15/2024 |
| 2340 | Ansh Labs Webster, TX Jr. Scientist Bachelor’s degree in Biological/Chemical Sciences/Biotechnology or related area. Exp: 1 year |
As a key member of the Manufacturing, Research & Development and Quality Control departments, this individual will provide critical scientific skills to assist in the development, scale-up and QC testing of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays). | 10/15/2024 |
| 2341 | Applied Medical Rancho Santa Margarita, CA Electrical Engineer II Bachelor's degree in electrical engineering or related engineering Exp: 1-2 years |
As an Electrical Engineer II at Applied Medical, you will play a crucial role in designing, developing, and testing electrical systems and components for medical devices. You will collaborate with cross-functional teams to ensure that the electrical systems meet product requirements and comply with regulatory standards. Additionally, you will contribute to the troubleshooting and resolution of electrical issues, ensuring the safety and reliability of the medical devices. | 10/15/2024 |
| 2342 | Applied Medical Rancho Santa Margarita, CA Manufacturing Process Engineer II Bachelor’s degree in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-2 years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. As a Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. | 10/15/2024 |
| 2343 | Applied Medical Rancho Santa Margarita, CA Process Engineer II/III Bachelor’s degree in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-4 years |
As a Process Engineer, you will work within the Group Process Development team and use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. The Process Engineer’s primary responsibilities are debugging, observing, and expediting shop orders. You will assist with developing and updating engineering documents and investigating new tooling, materials, manufacturing processes, and technologies. | 10/15/2024 |
| 2344 | Applied Medical Rancho Santa Margarita, CA Quality Systems Engineer I/II – Test Method Validation Bachelor's Degree or higher in Engineering or a scientific field. Exp: 1 year |
Join our innovative team as a Quality Engineer, where you will play a pivotal role in ensuring the highest standards of medical device safety and efficacy. Specializing in Test Method Validation, you will spearhead critical assessments to guarantee that our testing processes are precise, reliable, and compliant with regulatory standards. Your expertise will directly contribute to advancing healthcare solutions, impacting patient lives worldwide. | 10/15/2024 |
| 2345 | Aprecia Pharmaceuticals Blue Ash, OH Quality Analyst I B.S. degree in scientific discipline Exp: 1-2 years |
This position is primarily responsible for providing Quality support for manufacturing operations. Perform review of GMP documentation including manufacturing and packaging batch records, manufacturing logbooks, material specifications, and other quality documentation as assigned. Assist with ‘QA (Quality Assurance) on the Floor’ duties, including support for Manufacturing during production by providing room inspection and clearances, equipment inspection and clearances, and other quality checks required during the manufacturing and packaging processes. Writing and reviewing standard operating procedures and technical documentation for the storage, manufacture, testing, and distribution of products manufactured. Provide quality oversight, document review and guidance for other departments. Support other areas of Quality Assurance including Quality Systems and Quality Control, as designated by management. | 10/15/2024 |
| 2346 | Argonaut Manufacturing Services Carlsbad, CA Bioprocess Technician II Bachelor's degree in a related field Exp: 1 year |
The Bioprocess Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. | 10/15/2024 |
| 2347 | Argonaut Manufacturing Services Carlsbad, CA Formulation Technician II Bachelor's degree in a related field Exp: 1 year |
The Formulations Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. | 10/15/2024 |
| 2348 | Argonaut Manufacturing Services Carlsbad, CA Manufacturing Technician II Bachelor's degree in a related field Exp: 1 year |
The Manufacturing Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. | 10/15/2024 |
| 2349 | ARL Bio Pharma Oklahoma City, OK Chemist I - Analytical Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 10/15/2024 |
| 2350 | ARL Bio Pharma Oklahoma City, OK Chemist I - Chemistry Bachelor’s degree in chemistry or related science Exp: 0-2 years |
This position assists in maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position provides a backup for the daily calibration and/or verification of the balances and pH meter when the Lab Technician is unavailable. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform tests commensurate with skill level with some supervision. | 10/15/2024 |
| 2351 | ARL Bio Pharma Oklahoma City, OK R&D Scientist I Bachelor’s degree in chemistry or related science Exp: 0-2 years |
The position requires the performance of variety of task including development and validation of analytical methods and qualitatively/quantitatively testing routine and non-routine client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation (HPLC/IC) used in a chemistry laboratory. Research Scientist I work with direct supervision and reports to the lab supervisor. The Research Scientist I must be able to think and work independently, yet share ideas and work toward team goals. Ability to express thoughts in a clear concise manner both orally and written is also expected. Works to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities. | 10/15/2024 |
| 2352 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 10/15/2024 |
| 2353 | Arthrex Naples, FL Research Operations Specialist Bachelor’s degree required, preferably in life sciences related field. Exp: 1 year |
Manages with autonomy and independent judgement the daily activities of the Department of Orthopedic Research that supports critical operations and functions. Responsible for departmental strategic development and surgeon collaborations. Spearhead key inter- and intra-departmental initiatives. | 10/15/2024 |
| 2354 | AskBio Durham, NC QC Sample Coordinator Bachelor’s Exp: 1+ years |
The Sample Coordinator, reporting to the Lab Operations Manager in Quality Control, will be responsible for sample handling, management, and transport within the Quality Control and Analytical Development laboratories along with all procedures and processes governing sample activities. | 10/15/2024 |
| 2355 | Astellas Westborough, MA Quality Systems Engineer Masters degree Exp: 1+ years |
The Quality Systems Engineer role participates in the development and execution of key compliance functions within the larger GMP Quality Assurance department. This position indirectly supports ongoing manufacture of biological clinical trial materials by providing timely and compliant support for quality systems including Change Control administration, Calibration / Validation review, MasterControl system administration and workflow development, inspection management and hosting, internal auditing, supplier management, site Quality Council, quality metrics generation, and site-level compliance deliverables. | 10/15/2024 |
| 2356 | Astellas Seattle, WA Research Associate II, Molecular Analytics MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the molecular engineering for our gene edited Universal Donor Cells with activities focused on performing custom TaqMan based PCR assays. They will work as a key member on a fast-paced team to run molecular assays to characterize our proprietary Universal Donor Cells. | 10/15/2024 |
| 2357 | Astellas Westborough, MA Quality Assurance, Compliance Specialist MS Degree Exp: 0-2 years |
This member of the Quality Assurance team will perform critical QA compliance tasks in support of GMP manufacturing programs as AIRM moves through clinical trials and commercialization. The successful candidate will foster compliance across a broad range of Quality Assurance areas and will work closely with talented counterparts in the Manufacturing, Quality Control, and Materials Management teams to help ensure high quality standards and value delivery for our patients. | 10/15/2024 |
| 2358 | Astellas Westborough, MA QC Associate II, Raw Materials MS Degree Exp: 0-2 years |
Astellas, Westborough is seeking a highly motivated individual with strong organizational skills to join us as a QC Analyst II, Raw Materials. This position provides Quality Control compliance and release testing of raw materials used in the manufacture of Astellas cell therapy products in accordance with GDP/GMP guidelines. | 10/15/2024 |
| 2359 | Bio-Techne San Marcos, CA QC Specialist Bachelor’s degree in Biological Science, Chemistry, or related field. Exp: 1-5 years |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. | 10/15/2024 |
| 2360 | Bio-Techne Minneapolis, MN Research Associate Bachelor’s degree in biochemistry, microbiology, biotechnology,?or equivalent Exp: 0-2 years |
This position is responsible for the growth of E. coli in a GMP (Good Manufacturing Practice) Lab, following GMP guidelines. This includes, but is not limited to GMP, AF (Animal Free Process), and other products used by pharma and IVD customers. This position manufactures E. coli clones using shake flask, or Bioreactors using a variety of techniques, software and equipment including, Bioreactors, Shake Flasks, Biosafety cabinets, Fume Hoods, Sterile Filters, Autoclaves, and centrifuges. All procedures and batch records follow GMP guidelines. | 10/15/2024 |
| 2361 | Bio-Techne Minneapolis, MN Advanced Research Associate Master’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday - Saturday shift. | 10/15/2024 |
| 2362 | Bio-Techne Minneapolis, MN Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday - Saturday shift. | 10/15/2024 |
| 2363 | Bio-Techne Wallingford, CT Quality Technician Bachelor of Science degree in relevant field Exp: 0-2 years |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products. | 10/15/2024 |
| 2364 | Bio-Techne Minneapolis, MN Research Associate, Protein Purification GMP Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 10/15/2024 |
| 2365 | Bio-Techne Minneapolis, MN Manufacturing Technician Bachelors of science in biotech, chemistry, Biology, or engineering related field Exp: 0-3 years |
The successful applicant will work with other members of the reagent prep production team as well as a multidisciplinary team of engineers and scientists to support routine production activities for reagent formulation. | 10/15/2024 |
| 2366 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, Oligonucleotide Chemistry Bachelor's or Master'sdegree in Chemistry or related scientific discipline Exp: Bachelor's: 1 year Master's: 0-2 years |
The candidate will join a dynamic team responsible for the design and synthesis of oligonucleotides for Atalanta’s drug discovery programs. Successful candidates will have experience with modern laboratory equipment, and spectroscopic analysis, preferably in relation to oligonucleotides, as well as demonstrated ability to work as part of an integrated team on multiple parallel projects. This individual will be responsible for the independent operation and maintenance of instruments to synthesize, purify, and analyze chemically modified oligonucleotides as well as prepare samples for in vitro and in vivo studies. The ideal candidate is personable, organized, and thrives in a fast-paced environment. This role provides the right candidate with the opportunity to take on increasing responsibility over time within Atalanta’s Chemistry function. | 10/15/2024 |
| 2367 | Nestlé Health Science Bohemia, NY Associate Chemist (2nd Shift) Bachelor's Degree in Chemistry or closely relate discipline Exp: 0-4 years |
As an Associate Chemist, you will play a vital role in performing routine laboratory procedures. Your responsibilities will include conducting various tests and analyses under general supervision. To excel in this role, you should have a strong familiarity with basic laboratory equipment and techniques. Your focus will primarily be on conducting less complex testing and providing valuable support functions to ensure the smooth operation of the laboratory. This position offers a dynamic and collaborative work environment, where you will have the chance to work alongside a team of dedicated chemists. You will have the opportunity to enhance your skills and knowledge in a supportive setting. If you are passionate about laboratory work and are eager to contribute to our quality control efforts, we encourage you to apply for this exciting opportunity as an Associate Chemist. | 10/08/2024 |
| 2368 | Nestlé Health Science Savannah, GA Associate Process Project Engineer Bachelor's degree (Preferred mechanical, food or chemical engineering) Exp: 1+ years |
Learn and develop the skills in the design of processing and packaging equipment and manufacturing line taking into consideration the safety, quality and line performance. Provide technical inputs to team members and factory staff applying his/her academic subject expertise to practical applications at the manufacturing shop floor. Aid plant engineering to drive continuous improvement or capital projects from inception through all the stages feasibility and project handover. Assist in the implementation of Asset Maintenance Management systems, and other performance improvement activities to reduce improve line performance, reduce TDC and ensure compliance. | 10/08/2024 |
| 2369 | Nestlé Health Science Bohemia, NY Industrial Engineering Specialist Bachelor of Science degree in Industrial Engineering/Engineering Exp: 1-3+ years |
The Industrial Performance Engineer will be responsible for identifying and driving operational improvement and cost savings projects. Continuous improvement efforts will focus on making sustainable gains in reliability, quality, safety, cost, and delivery. Methods for achieving and sustaining improvements will be based Nestle Continuous Excellence and TPM fundamentals. The team member will need to collaborate closely with Operations and other internal partners to achieve the project objectives aligned with the NHS business needs. The team member will be responsible to carry out assignments of a broad nature while exercising considerable judgment and creativity. The team member needs to be able to carry out appropriate financial analysis to validate/support proposals and gain support of key stakeholders. | 10/08/2024 |
| 2370 | Nestlé Health Science Sudbury, MA Quality Associate Bachelor’s Degree in a Science field Exp: 1 year |
Review all paperwork issued by Quality Associate before release for Production Department. Oversee the quality of the products manufactured and sold. Assist Product QA Supervisor & Quality Director in development of quality control and quality assurance programs. | 10/08/2024 |
| 2371 | Ajinomoto Bio-Pharma San Diego, CA Microbiology Associate I - 2nd Shift Bachelor’s degree in a Life Sciences discipline Exp: 1-2 years |
We are currently seeking a Microbiology Associate I – 2nd Shift. This position is responsible for supporting manufacturing at Ajinomoto Bio-Pharma Services. The Microbiology Associate I may focus in a specialized area and provide routine analysis and testing according to standard operating procedures in any of the following areas: in process and final product testing and microbiology assays including TOC, conductivity, bioburden, endotoxin, and growth promotion | 10/08/2024 |
| 2372 | Ajinomoto Bio-Pharma San Diego, CA Drug Product Manufacturing Associate I Bachelors in a science or engineering discipline Exp: 0-2 years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 10/08/2024 |
| 2373 | Akoya Biosciences Marlborough, MA Research Associate II BA or MSc in Life Sciences Exp: 1 year |
As a Research Associate II, you will work in a dynamic, team-oriented environment and take part in developing multiplex fluorescent immunohistochemistry (IHC) Reagents products for use in cutting- edge research. The desired skillset for laboratory work includes the ability to perform conventional immunohistochemistry (IHC), antibody conjugation, assay development for multiplex fluorescent staining. The candidate will be responsible for antibody validation, staining protocol optimization, and image analysis. In this role, you must be able to perform the following tasks independently: experiment setup and execution, reagents preparation, data analysis and protocol troubleshooting. | 10/08/2024 |
| 2374 | Alamar Biosciences Fremont, CA Lab Technician, Quality Control Bachelors degree in a scientific field Exp: 1-2 years |
We seek a highly motivated Lab Technician, Quality Control to join a dynamic team of professionals in the Operations team to support our company mission. This position will be working in the Quality Control team to support incoming receiving & inspections, visual inspections, analytical testing, and laboratory and equipment maintenances activities. Seeking a professional that is a quick learner, organized, detail oriented, and can handle shifting priorities in a fast-paced and rapid growing company, while adhering to established protocols and procedures in compliance to ISO 13485/GMP requirements. | 10/08/2024 |
| 2375 | Alcami Morrisville, NC Manufacturing Technician I - 2nd Shift Bachelor’s degree Exp: 0-1 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and is responsible for maintaining product quality by supporting GMP operations of life-saving sterile injectable drug products intended for clinical trials and commercial distribution. The Manufacturing Technician I operates in alignment with established Standard Operating Procedures (SOPs) and approved Batch Records, which are developed in accordance with regulatory expectations and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable cleanroom techniques while working in manufacturing/inspection environments and is expected to demonstrate proficiency in all department procedures and provide manufacturing updates to area supervision. | 10/08/2024 |
| 2376 | Alcami Morrisville, NC Manufacturing Technician II - 1st Shift Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician II is accountable for results in a fast-paced environment and is responsible for maintaining product quality by supporting GMP operations of life-saving sterile injectable drug products intended for clinical trials and commercial distribution. The Manufacturing Technician II operates in alignment with established Standard Operating Procedures (SOPs) and approved Batch Records, which are developed in accordance with regulatory expectations and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician II employs acceptable cleanroom techniques while working in manufacturing/inspection environments and is expected to demonstrate proficiency in all department procedures and provide manufacturing updates to area supervision. | 10/08/2024 |
| 2377 | Alcami Morrisville, NC Manufacturing Technician II - 2nd Shift Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician II is accountable for results in a fast-paced environment and is responsible for maintaining product quality by supporting GMP operations of life-saving sterile injectable drug products intended for clinical trials and commercial distribution. The Manufacturing Technician II operates in alignment with established Standard Operating Procedures (SOPs) and approved Batch Records, which are developed in accordance with regulatory expectations and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician II employs acceptable cleanroom techniques while working in manufacturing/inspection environments and is expected to demonstrate proficiency in all department procedures and provide manufacturing updates to area supervision. | 10/08/2024 |
| 2378 | Alcon Johns Creek, GA Senior Engineer Associate Injection Molding Engineer M.S. Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Senior Engineer Associate Injection Molding, you will be trusted to research, plan, design, develop, optimize and maintain injection molding processes. This includes part design, tooling, injection molding equipment, process optimization, and molded part measurement systems. Applies knowledge of injection molding principles to improve part design, specify tooling and molding equipment, optimize molding processes and trouble shoot injection molding processes. | 10/08/2024 |
| 2379 | Alcon Fort Worth, TX Senior Scientist M.S. Exp: 0+ years |
Developing new analytical methods and designing experiments that push boundaries of understanding. Advancing analysis of starting materials, in-process materials and finished products, ensuring the highest quality at every stage Documenting experiments, preparing technical documents, writing sections of regulatory documents and communicating and collaborating with colleagues and supervisors. Participating in functional teams and lab meetings offer assistance to co-workers and possibly leading a functional sub-team as expected. Applying chemistry and analytical technical skills to complete assigned work and solves routine problems. Ensuring products meet stringent standards for eye care, designing multiple studies. | 10/08/2024 |
| 2380 | Alcon Johns Creek, GA Senior Associate - Metrology M.S. Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Senior Associate - Metrology supporting our Research and Development Engineering Team, you will lead and support metrology activities within the organization to ensure measurement accuracy and compliance with industry standards. You will be responsible for developing, implementing, and maintaining measurement systems, procedures, and equipment calibration processes at our R&D site in Johns Creek, GA. | 10/08/2024 |
| 2381 | Alcon Johns Creek, GA Validation Engineer M.S. Exp: 0+ years |
As a Validation Engineer supporting the U.S. Development of Characterization and Qualification Team in Duluth, GA. | 10/08/2024 |
| 2382 | Aldevron Fargo, ND Quality Control Environmental Analyst I Bachelor’s degree in microbiology or related scientific field Exp: 0-1 years |
This position is part of the Quality Control department located in Fargo, ND and will be an on-site position. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Quality Control Environmental Monitoring Team and report to the QC Environmental Monitoring Supervisor, and be responsible for sampling, detecting, quantifying, and identifying possible contaminants that may interfere with the quality of the product during the different stages of the manufacturing process. | 10/08/2024 |
| 2383 | Aldevron Madison, WI Associate Scientist II, R&D BS or MS degree in biology, molecular biology, biochemistry, chemistry, or related discipline Exp: BS: 1+ years; MS: 0+ years |
This position is part of the Research and Development Department located in Madison, WI and will be onsite. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Analytical Method Development team and report to the Senior Scientist responsible for analytical method development and new method research. | 10/08/2024 |
| 2384 | Alexza Fremont, CA Data Review I, Quality Control BS degree in scientific area or equivalent Exp: 0-2 years |
Perform timely data review with a high focus on data quality to ensure accuracy, completeness, cGMP compliance of QC test data. Verify data transfer, calculations and documented information such as reagent expiry, instrument calibration, logbook entries, standards, controls, etc. are present, complete and accurate. Verify that all analysis performed were as per test method and/or compendial methods and were in compliance with GMP requirements. Data review included but limited to QC testing data supporting product release, incoming material testing; stability studies, and qualification/validation/verification related studies. Complete training for test methods in a timely manner. Utilize knowledge of good documentation practices and good laboratory practices on a daily basis. Other duties as assigned. | 10/08/2024 |
| 2385 | AlivaMab Biologics San Diego, CA Research Associate II - Sequencing and Molecular Biology MS in Molecular Biology, Biomedical Engineering, or a related scientific field Exp: 1-3 years |
AlivaMab Biologics is seeking an outstanding individual to join the Antibody Engineering Team. The successful applicant will have the responsibility to support antibody discovery and engineering projects through Next-Generation Sequencing (NGS) of various samples including, but not limited to, hybridomas, single B-cells, immune repertoires, and phage libraries. The individual will also perform molecular cloning and contribute to technology development in the Molecular Biology group. This position will report to the Principal Scientist, Sequencing and Molecular Biology, and work closely with scientists in the Protein Sciences and Antibody Discovery teams. | 10/08/2024 |
| 2386 | Allogene Therapeutics Newark, CA Associate, Cell Therapy Manufacturing (Contract) Bachelors or Associates in relevant science or engineering discipline Exp: 0-2 years |
We are seeking a highly motivated Associate, Cell Therapy Manufacturing to join our Manufacturing team. This is a contract role. This role will work within the Manufacturing team in supporting our efforts in an exciting new area of cancer immunotherapy. This position is based out of Newark, CA. They will work within the Manufacturing team in supporting our efforts in an exciting new area of cancer immunotherapy. This position is based out of Newark, CA. The position will report to the Senior Manager, Manufacturing and will support the successful tech transfer and operational readiness process, using knowledge of cGMP regulations to ensure manufacturing readiness. Responsibilities of primary importance are: to ensure the successful, time-sensitive GMP manufacture and release of cell therapy products; to follow all processes and procedures related to operations in full compliance with cGMP, CFRs, site quality systems and company policies; and to promote a culture of quality and compliance. The successful candidate will have experience in a regulated biotech or pharmaceutical setting and will have proven competency and expertise in the GMP manufacture of cell-based therapies. | 10/08/2024 |
| 2387 | Alloy Therapeutics Waltham, MA Research Associate – Oligonucleotide Discovery B.S. or M.S. degree in Biology or related science Exp: 1-3 years |
As a Research Associate, you will work within the RNA Medicine team in Waltham, MA. You will also collaborate with internal/external partners on nucleic acid drug discovery projects to ensure timely execution of the experiments, and delivery of high-quality data. This role will have an autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This is you! This role will report to our RNA Senior Scientist with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This is you! | 10/08/2024 |
| 2388 | Alltrna Cambridge, MA Senior Research Associate, Medicinal Chemistry MS degree in Chemistry, Biochemistry, or related discipline Exp: 1+ year |
We are looking for a passionate, creative scientist to join and our growing medicinal chemistry team focused on the advancement of our tRNA therapeutic platforms. This effort is driving forward a deeper mechanistic understanding of synthetic tRNA molecules. The successful candidate will join our highly innovative RNA/oligonucleotide synthesis team and have a strong background in oligonucleotide chemistry through hands-on experience in the synthesis, downstream process, characterization and purification of oligonucleotides. This individual would be part of the team that writes the textbook for developing tRNA molecules for therapeutics and be critical not only in ensuring that we can understand how our tRNA molecules are synthesized using automated systems but also in defining how we support our drug discovery and development efforts. We operate in an open and inclusive learning environment and need nimble thinkers who can chart courses and plan experiments based upon the data that we generate together. | 10/08/2024 |
| 2389 | Almac Group Durham, NC QC Inspector Grade 1 Bachelor's degree with science background Exp: 6+ months |
Almac Group is currently seeking a Quality Control Inspector Grade 1 for our Durham, NC location. The Quality Control Inspector will inspect operational activities for compliance to cGMPs, Almac SOPs, and other written quality and customer standards. | 10/08/2024 |
| 2390 | Vertex Boston, MA Discovery Biology Senior Research Associate Master's Degree in biological sciences Exp: 0-2 years |
Vertex is building out a Discovery Biology group focused on fundamental human biology, pushing the frontiers of stem cell biology to pursue curative cell therapies in multiple disease areas. The Discovery Biology Senir Research Associate performs a variety of well-defined support functions and participates in research activities, including the development of human stem cell models and assays to evaluate targets and lead molecules for Vertex diseases. | 10/08/2024 |
| 2391 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 10/08/2024 |
| 2392 | Altasciences Columbia, MO Associate Scientist- Lab Sciences MS in biological, pharmaceutical science or related field Exp: 1 year |
Are you an experienced candidate looking for a new opportunity and a growing and innovative company? Altasciences is looking for you. We need someone who can provide technical and scientific leadership in the area (e.g., spectrophotometry, chromatography, ligand assay, flow cytometry, molecular biology). Plan and executes projects, and identifies and acquires the necessary facilities, equipment and procedures for research projects by performing the below duties. | 10/08/2024 |
| 2393 | Altasciences Columbia, MO Research Associate Bachelors degree in scientific discipline Exp: 1 year |
The Research Associate, Laboratory Sciences role assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. Support and perform data collection activities including qPCR, DNA isolation, ligand binding assays, and flow cytometry, as assigned. | 10/08/2024 |
| 2394 | AltPep Corporation Seattle, WA Senior Research Associate Master’s degree Exp: 1+ year |
We are seeking a meticulous and dynamic Senior Research Associate to join our translational chemistry team. As part of this role, you will be responsible for conducting and supporting laboratory research, ensuring the highest standards of quality and precision. Your contributions will be critical to the success of our research and development efforts, and you will have opportunities to work both independently and collaboratively within our innovative team. | 10/08/2024 |
| 2395 | Alvogen Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline Exp: 0-3 years |
The Quality Control Chemist I: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. | 10/08/2024 |
| 2396 | Amador Bioscience Pleasanton, CA Scientist - Bioanalysis & Biomarkers- LCMS Master’s, or Bachelor’s degree in biology, immunology, chemistry, pharmacology, or other related scientific fields Exp: 0-9 years |
Amador Laboratory Services Division specializes in bioanalysis (PK/PD/ADA), biomarkers, assay development & validation, and sample analysis. The team has successfully supported multiple non-GLP, GLP (nonclinical) and GCLP (clinical) projects. To meet the needs of business growth, we are looking for a highly motivated, experienced scientist/senior scientist to join our passionate team to partner with our clients for success. The successful candidate will be responsible for providing bioanalytical supports for both pre-clinical and clinical projects and will report to the Laboratory Head. | 10/08/2024 |
| 2397 | American Regent Brea, CA Validation Technician Bachelor degree in field of science Exp: Entry Level |
The Validation Technician will be responsible for supporting the qualification process of manufacturing equipment, facility utilities and storage chambers to ensure that all criteria satisfy FDA and cGMP guidelines for facility use. This position will also perform routine monitoring activities (such as routine monitoring of temperature-controlled chambers / areas and cleanroom pressure differentials) within the facility. | 10/08/2024 |
| 2398 | American Regent New Albany, OH QA Operations Associate I- 2nd Shift Bachelor’s Degree Exp: 1 year |
This position is responsible for ensuring the overall Quality in their assigned areas through the execution of site policies and procedures, programs and work instructions. Ensures all processes and products meet specifications and that products are produced in accordance with GMP requirements. | 10/08/2024 |
| 2399 | American Regent Columbus, OH QC Microbiologist I Bachelor’s degree in Microbiology, Biology, or equivalent Life Science curriculum Exp: 1 year |
This position in the Microbiology Laboratory will be primarily responsible for performing, coordinating and tracking the microbiological testing for in-process and finished products as well as monitoring of controlled manufacturing facilities and utility systems. | 10/08/2024 |
| 2400 | American Regent Columbus, OH Sterility Assurance Scientist I Bachelor’s Degree in Microbiology, Biology or related field Exp: 1 year |
This position in the Sterility Assurance Department will be primarily responsible for writing investigations/Excursions for Environmental and Personnel Monitoring with regards to assurance of sterility and being involved in technical projects from protocols to final reports. | 10/08/2024 |
| 2401 | Amgen Thousand Oaks, CA Sr. Associate (Process Development) Master’s degree in Chemical Engineering, Biomedical Engineering, Biochemistry, Biotechnology, Pharmaceutics or related subject area Exp: 1+ years |
Amgen is currently seeking a Process Development Senior Associate for our Pivotal Drug Product Technologies Group in Thousand Oaks, CA. This group is responsible for late stage drug product formulation and fill/finish process development for large molecule modalities (e.g. monoclonal antibodies, bispecific T-cell engagers (BiTEs) and fusion proteins). The Sr. Associate will work closely with a team of engineers and scientists responsible for the technical aspects of Amgen’s drug product commercialization and lifecycle management. | 10/08/2024 |
| 2402 | Amneal Piscataway, NJ Scientist II, Quality Control Master Degree (MBA) Chemistry or related science discipline Exp: 1+ year |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 10/08/2024 |
| 2403 | Amneal Piscataway, NJ Scientist I, Quality Control Bachelors Degree (BA/BS) in Chemistry or related field Exp: 1 year |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 10/08/2024 |
| 2404 | Amneal Brookhaven, NY Scientist I, Quality Control Bachelors Degree (BA/BS) in Chemistry or related field Exp: 1 year |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 10/08/2024 |
| 2405 | Amneal Brookhaven, NY Validation Engineer I, Engineering Bachelors Degree (BA/BS) in Pharmaceutical manufacturing, Engineering, Science or relevant field Exp: 0-2 years |
The Validation Engineer I provides support in performing equipment, facility and utility qualification activity and re-qualification activity to ensure compliance to cGMP and Amneal's quality requirements. | 10/08/2024 |
| 2406 | Amneal Branchburg Township, NJ Scientist II, Quality Control Technical Services Master Degree (MBA) in Chemistry or related science discipline Exp: 1+ years |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 10/08/2024 |
| 2407 | Abeona Therapeutics Cleveland, OH Quality Assurance Specialist, Supplier Quality Bachelor’s degree in related field Exp: 1 year |
The Specialist I, Supplier Quality will perform routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the release of materials in support of cGMP Operations. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above. | 09/30/2024 |
| 2408 | Abeona Therapeutics Cleveland, OH Quality Control Transport/Microbiology Associate BS in biology, microbiology, molecular biology or other relevant discipline Exp: 1-4 years |
The Quality Control Transport/Microbiology Associate assists in all aspects of Transport of Drug Products to treatment centers for the associated drug product. In addition, Transport associate will assist in Microbiology activities in support of GMP testing for Quality Control. Interacts with employees internal and external to Quality Control. | 09/30/2024 |
| 2409 | Abeona Therapeutics Cleveland, OH Sr. Associate, Manufacturing - Logistics QMS BS in life sciences, engineering, or other relevant discipline Exp: 1-4 years |
The Manufacturing Logistics QMS Senior Associate is responsible for working independently and with others to perform Quality Management System activities pertaining to the Manufacturing Department. This individual serves as an embedded quality assurance representative within the Manufacturing Department. | 09/30/2024 |
| 2410 | Abzena Bristol, PA Associate Scientist II, PD Chemistry B.Sc. in Chemistry or Chemical Engineering Exp: 1-2 years |
The Associate II will conduct research, troubleshoot, and solve problems arising during synthetic route/process development. The associate II will safely execute synthetic processes adhering to EHS and regulatory guidelines. | 09/30/2024 |
| 2411 | Abzena Bristol, PA Scientist I, PD Chemistry B.S or M.Sc. degree in Chemistry or Chemical Engineering Exp: 1-3 years |
The ability to design and conduct research, troubleshoot, and solve problems arising during synthetic route/process development. Develop safe and efficient synthetic processes that can be scaled-up reliably and reproducibly adhering to EHS and regulatory guidelines. | 09/30/2024 |
| 2412 | ICON Salt Lake City, UT Senior Laboratory Assistant Bachelor’s degree (preferred) Exp: 1 year |
We are currently seeking a Senior Laboratory Assistant to join our diverse and dynamic team at ICON at our Salt Lake City UT site. The Senior Lab Assistant aids the technical staff with the handling and storing of and accounting for biological lab specimens, quality control and any other relevant tasks. | 09/30/2024 |
| 2413 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s degree in biology or a related field Exp: 0-3 years |
We are looking for a Research Associate to perform key tasks that are vital to our research services. The primary focus of this role involves molecular and cellular biology techniques, including DNA cloning, plasmid DNA preparation, site-directed mutagenesis, mammalian cell culture, cell transfection, stable cell line generation, FACS analysis, cell-based assays, and general lab maintenance. | 09/30/2024 |
| 2414 | Accutar Biotech Cranbury, NJ Medical Scientist (Drug Discovery Project Manager) Master in Medicine Exp: 1 year |
Coordinate and lead medical drug discovery clinical trial projects. Design and develop plans and process for specific drug during clinical trial process. Manage investigational product supplies and participate internal audits. Develop and review specific research-related documents. Develop and coordinate research project budget, management project progress and review project performance. Collect feedbacks and data from clinical trials and prepare reports for improvement of drug performance. Manage outsourced Central Lab activities. Serve as the contacts with partners and government agency in drug approving processing. | 09/30/2024 |
| 2415 | Accutar Biotech Mountain View, CA Senior AI Chemist Master’s degree in Chemistry or Chemical Engineering required Exp: 1 year |
Conduct qualitative and quantitative chemical analyses of lab data for our drug discovery pipelines with the assistance of developed artificial intelligence (AI) empowered platform. Write technical papers and reports. Prepare standards and specifications for operational protocols of drug discovery platform. Coordinate operations of company’s medchem lab. Coordinate the drug discovery projects within with outsourcing researcher and in house researchers. Collaborate with computation department to improve theefficiency, scalability and precision of our drug-discovery platform. | 09/30/2024 |
| 2416 | Acepodia Alameda, CA Research Associate I/II B.S. or M.S. in life science-related fields (Immunology, Molecular Biology, Pharmacology, Chemistry, and Biochemistry) Exp: Recent Graduate/Entry Level |
Acepodia is seeking a self-motivated and detailed-oriented individual with a passion for the translational research and pipeline development. This is an excellent opportunity for a recent graduate with a strong foundation in molecular biology and immunology to gain hands-on experience in a research and translational environment. The position involves both hands-on laboratory work and the translational activities essential to developing novel therapies. You will work in a supportive and collaborative cross functional team with R&D and clinical team members across the US and Taiwan. | 09/30/2024 |
| 2417 | AstraZeneca Gaithersburg, MD Associate Specialist Clinical Biologics Bachelor's degree Exp: 0-4 years |
As an Associate Specialist/Specialist in the Clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities. Under the supervision of highly trained personnel, you will gain the process knowledge and skillsets to perform large scale clinical development activities. You will join a collaborative and driven team in an elite biopharmaceutical company. | 09/30/2024 |
| 2418 | AstraZeneca New Haven, CT Associate Scientist II, Injectable Drug Product Development Master’s degree in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or relevant Engineering/Life Sciences field Exp: 1+ years |
The Associate Scientist III will join Injectable Drug Product Development group to support the formulation and drug product process development of Alexion’s biotherapeutic candidates. This individual will lead and support execution of stability studies, develop fit for purpose analytical methods, perform analytical testing, and draft reports for the executed studies. This individual will work independently in a dynamic team environment and routinely collaborate with other members of Injectable Drug Product Development as well as other groups in Product Development and Clinical Supply. A general understanding of protein chemistry and machine learning based image analysis is preferred. | 09/30/2024 |
| 2419 | AstraZeneca Santa Monica, CA Associate, Quality Control Analytical Master's degree in Biological Sciences or related field Exp: 1 year |
Neogene is looking for an energetic and experienced person with cell therapy quality control background to join our Quality Control (QC) team. You will contribute to the advancement of our product pipeline by performing QC analytical method qualification, complete sample analysis, and other assigned tasks. You will also independently organize and present results and conclusions. You will ensure that the QC Analytical laboratory is operating as expected. | 09/30/2024 |
| 2420 | AstraZeneca Gaithersburg, MD Scientist, OTD Target Validation Master’s Degree in relevant discipline Exp: 1+ years |
We are seeking highly a motivated independent lab Scientist with wet-bench laboratory experience to join our Tumor Targeted Delivery team in Early Oncology in Gaithersburg, MD USA. As a Scientist, you will support target validation efforts for tumor-targeted therapies, such as antibody-drug-conjugates (ADCs) and targeted radio-conjugates. You will work collaboratively with cross-functional teams to advance pipeline programs and deepen our understanding of all aspects of target biology. | 09/30/2024 |
| 2421 | AstraZeneca Santa Monica, CA Senior Associate, Quality Control Microbiology MS/MA Exp: 1+ years |
We are seeking an individual with cell therapy quality control background to join our Quality team. You will contribute to the advancement of our product pipeline by performing environmental monitoring, lot release testing and other assigned tasks. You will also be expected to independently organize, analyze results, and present conclusions. You will ensure that the QC Microbiology Laboratory is operating as expected. | 09/30/2024 |
| 2422 | AstraZeneca Gaithersburg, MD Scientist in vivo - Immunology MS Exp: 1 year |
The successful candidate will be a key member of an in vivo team within the Early Respiratory & Immunology in vivo Department, performing in vivo and ex vivo studies to support a diverse range of immunology-related projects. This role specifically involves working as a lab-based scientist in the area of in vivo pharmacology. As a strongly self-motivated and independent individual you will be adept at working across functional areas, enabling you to maximize value from the available resources. The role will sometimes involve implementing protocols over timelines that extend outside of normal working patterns. The successful candidate will assist with the design, execution and analysis of experiments to generate data in support of pipeline projects. You will be expected to utilize your expertise to run various in vivo disease models, as well as provide input for the establishment of new in vivo models. | 09/30/2024 |
| 2423 | AstraZeneca Frederick, MD Electrical Engineer BA/BS in Engineering/Life Sciences Exp: 0-5 years |
As an Electrical Engineer, you will be responsible for a wide range of tasks including troubleshooting motor controls, performing BMS changes, supporting automation for electrical and utility systems, and implementing operational improvements to reduce energy consumption. You will also be involved in project management, problem-solving, and communication with internal teams and external vendors. Your work will contribute to the completion of milestones associated with specific activities and you will be expected to lead moderate cross-functional teams to complete work. | 09/30/2024 |
| 2424 | Adare Vandalia, OH Analytical Scientist I Master’s Degree in Chemistry or related discipline Exp: 0-1 years |
The will support the development and validation of analytical methods for raw materials, work-in-process, and finished products and to provide testing support for the formulation development and clinical supplies release process. The Scientist II will also be expected to provide some training, coaching, and mentoring for more junior scientists. This position reports to the Manager, Analytical Sciences, R&D. | 09/30/2024 |
| 2425 | Adare Vandalia, OH QC Chemist I - 3rd Shift Bachelors Degree in Chemistry or related field Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 09/30/2024 |
| 2426 | Adesis Wilmington, DE Research Chemist Bachelor of Science Exp: 1-2 years |
Responsible for assisting chemists in performing various purifications of target compounds using various methods, including, but not limited to preparative high performance liquid chromatography (prep HPLC), normal phase and reverse phase chromatography, and recrystallization . | 09/30/2024 |
| 2427 | H.B. Fuller St. Paul, MN Scientist Master’s degree in chemistry or chemical engineering Exp: 1+ years |
The Scientist has primary responsibility for conducting research tasks coordinated by more experienced scientists and managers. In general, a Scientist conducts laboratory bench work tasks, physical testing and supports QA and Operations in trouble shooting manufacturing issues. This position is responsible for product development, cost saving initiatives, and production support. This person will be dealing primarily with moisture curing one-part and solvent free two-part technologies for adhesives, sealants, and coatings for the North America Construction Adhesives business. This includes building envelope, flooring, DIY, and other construction applications. | 09/30/2024 |
| 2428 | Adimab Lebanon, NH Research Associate - Molecular Biology B.S. or M.S. in molecular biology, cellular biology, biochemistry, or closely related field Exp: 1 year |
We are seeking an experienced Molecular Biologist to join our Antibody Library Team. The successful candidate will have prior experience in molecular or synthetic biology. The Research Associate will work in a small team to build our Antibody Library Platform. The associate will work closely with our antibody engineering and computational biology teams. | 09/30/2024 |
| 2429 | Adimab Lebanon, NH Research Associate - Antibody Engineering B.S., or equivalent practical experience, with training in molecular biology, chemical engineering, or biochemistry Exp: 1 year |
We are seeking a focused and enthusiastic protein engineer to join our Antibody Engineering group. The Research Associate will work in a small team setting, executing Adimab’s discovery platform on funded discovery and optimization projects and characterization of primary and optimized lead antibodies. | 09/30/2024 |
| 2430 | Admera Health South Plainfield, NJ Associate Scientist I/II (Lab) Bachelor’s or M.S. degree in Biological Sciences Exp: 1-3 years |
Admera Health is looking for an Associate Scientist I/II to join our growing team! Preparing solutions and reagents for performing assays on the bench. Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing. Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. Strict recordkeeping of all laboratory procedures. Continue acquiring next generation sequencing knowledge to support molecular biology techniques. Collaborate within the group and cross departmental to achieve goals. | 09/30/2024 |
| 2431 | Admera Health South Plainfield, NJ Project Specialist I M.S. in Biological Sciences Exp: 1-2+ years |
Admera Health is seeking a Project Specialist I to join our growing team! Admera Health provides genomic and bioinformatic services supporting discovery through clinical research stages. Our services include solutions for genomics, transcriptomics, epigenomics, and bioinformatics. Admera has deep expertise working with single-cell, FFPE, custom panels, and difficult or low-input samples. | 09/30/2024 |
| 2432 | B. Braun Medical Irvine, CA QC Chemistry Associate II (Chromatography) Bachelor's degree in a Science related field Exp: 1-2 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 09/30/2024 |
| 2433 | Affinia Therapeutics Waltham, MA Lab Technician, Analytical Development Bachelors degree in Biotechnology or related field Exp: 1-2 years |
Affinia Therapeutics is seeking an enthusiastic Lab Technician to join our Analytical Development laboratory team. As a member of the team, you will run analytic test methods for routine sample testing to support our process development and manufacturing activities. You will contribute to the evaluation of new analytical technologies and the development of more efficient laboratory workflows to maintain a culture of data quality and excellence. This position is located in our state-of-the-art facility in Waltham, MA. | 09/30/2024 |
| 2434 | Agathos Biologics Fargo, ND Laboratory Research Associate Bachelor’s degree in Biological Sciences or equivalent Exp: 1-5 years |
Agathos Biologics is seeking a Research Associate to join our team. The successful candidate will be responsible for following established protocols and conducting high-quality analytical testing. Attention to detail and accurate data reporting are crucial aspects of this role and important to the success of our company’s products and services. The ideal candidate will be highly organized, capable of working independently, and able to manage multiple projects simultaneously. | 09/30/2024 |
| 2435 | Agathos Biologics Fargo, ND Associate Scientist Bachelor’s degree in Biological Sciences or equivalent Exp: 1-5 years |
The Associate Scientist will conduct high quality scientific research and development to support the company’s goals and achieve their career objectives. | 09/30/2024 |
| 2436 | AGC Biologics Boulder, CO Quality Assurance Associate I Bachelor’s degree in biology, Chemistry or other relevant science/engineering discipline Exp: 0-2 years |
The Quality Assurance Associate I- III (In Plant Operations) is responsible for providing (24/7/365) Quality support to the activities listed below at the Boulder, CO site. One Colorado, one team. At our Boulder and Longmont locations, we cultivate a unified team under the banner of 'One Colorado', fostering collaboration among diverse teams and their respective business units. Together, we leverage a shared services objective between the two sites to enhance care for our clients and their patients. | 09/30/2024 |
| 2437 | AGC Biologics Boulder/Longmont, CO Downstream Manufacturing Associate I Bachelor’s degree Exp: 1 year |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. | 09/30/2024 |
| 2438 | AGC Biologics Boulder/Longmont, CO Upstream Manufacturing Associate I Bachelor’s degree Exp: 1 year |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. | 09/30/2024 |
| 2439 | AGC Biologics Bothell, WA Upstream Manufacturing Associate I BS/BA degree Exp: 0-2 years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor, and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. An Associate I assists with bioprocess operations in Manufacturing in compliance with established processes and standards. | 09/30/2024 |
| 2440 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I BS/BA degree Exp: 0-2 years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor, and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. An Associate I assists with bioprocess operations in Manufacturing in compliance with established processes and standards. | 09/30/2024 |
| 2441 | Agilent Remote - Pearl River, NY Field Service Engineer Bachelor’s or master's degree within the science field - e.g., chemistry, analytical chemistry biochemistry, biotechnology Exp: 1-2+ years |
Every day, Agilent Regional Field Service Engineer help our customers to tackle issues that enable scientists to make discoveries that improve the quality of life. Through our work, we deliver insights and provide support that keep labs running smoothly and more efficiently. Join our multifaceted organization to be a part of this exciting work. As a Field Service Engineer for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software and consumables is key. Applying your interpersonal skills, creativity and can-do attitude is essential. The ability to help with solving customer problems and a dedication to deliver the highest levels of customer service is how you will build customer success. | 09/30/2024 |
| 2442 | Agilent Boulder, CO Quality Control Analyst Bachelor’s Degree or equivalent experience in Analytical Chemistry or related life sciences field Exp: 1-3 years |
The Quality Control Analyst will conduct routine, non-routine analysis and review to support release, stability testing per Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements. Has a clear understanding of Good Laboratory Practices (GLPs), cGMPS, and other regulatory requirements. Effectively engages in continuous improvement of processes and procedures. Proven ability to exercise judgment and appropriately escalates issues to QC management. | 09/30/2024 |
| 2443 | Agilent Carpinteria, CA Research Laboratory Technician - Assays BS/BA in Biology, Biochemistry, or related field Exp: 0-2+ years |
We are looking for a hardworking and dedicated R&D Tech to join our CDx Research and Development Department. You will provide research support to develop accurate, robust, and precise assays. You will work in a cross-functional team dedicated to the design and development of CDx assays in a highly regulated environment. | 09/30/2024 |
| 2444 | Agilent Remote, TX Field Service Engineer Bachelors or Master’s degree within the science field - e.g., chemistry, analytical chemistry biochemistry, biotechnology Exp: 1-2+ years |
Every day, Agilent Regional Field Service Representative help our customers to tackle issues that enable scientists to make discoveries that improve the quality of life. Through our work, we deliver insights and provide support that keep labs running smoothly and more efficiently. Join our multifaceted organization to be a part of this exciting work. As a Field Service Representative for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software and consumables is key. Applying your interpersonal skills, creativity and can-do attitude is essential. The ability to help with solving customer problems and a dedication to deliver the highest levels of customer service is how you will build customer success. | 09/30/2024 |
| 2445 | Agilent Cedar Creek, TX Manufacturing Scientist - Genomic Reagents Testing Bachelor's degree in Biological Science or a related field with chemistry, molecular biology, or biochemistry Exp: 1 year |
Join our innovative team at Agilent Technologies as a Manufacturing Scientist specializing in genomic reagents. You'll contribute to ground breaking products that advance Next Generation Sequencing (NGS), Microarray testing, and PCR-based technologies. If you're passionate about driving scientific advancements and thrive in a dynamic, collaborative environment, this role offers an exciting opportunity to grow and make a tangible impact. | 09/30/2024 |
| 2446 | Agilent Remote - Boston, MA Field Service Engineer - Biomolecular, Genomics, and Cell Analysis Instrumentation Bachelor’s degree within the science or engineering field – e.g. chemistry, analytical, biomedical Exp: 0-2 years |
As a Field Service Engineer for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software and consumables is key. Applying your interpersonal skills, creativity and can-do attitude is essential. The ability to help with solving customer problems and a commitment to deliver the highest-levels of customer service is how you will build customer success. An Agilent Field Service Engineer supporting Biomolecular, Genomics, and Cellular Analysis instruments will travel to customer’s laboratories to install, maintain, and repair the Agilent instruments. These instruments are critical tools in the research, development, and manufacturing for several key areas including Cell and Gene Therapy, Infectious Disease, Virology and Vaccine Research, Immunology, Immuno-oncology, and Immunotherapy, as well as Next Generation Sequencing, and Pre-Natal Disease Detection. The Biomolecular Service Organization is an evolving and fast-growing part of Agilent’s Customer Service Organization supporting these growing and exciting markets. | 09/30/2024 |
| 2447 | Vivex Biologics Miami, FL IC/QC & Distribution Coordinator I Bachelors Exp: 0-1 years |
The IC/QC & Distribution Coordinator I - Weekend Shift is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Ensure that Inventory Control Operations are in Compliance with the State and Federal Regulations and AATB Standards. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Resourceful in completing deadlines and can multitask effectively. | 09/24/2024 |
| 2448 | Vivex Biologics Miami, FL Quality Assurance Engineer I Bachelor’s degree in engineering or a related technical discipline (e.g. Biology, Chemistry, etc.) Exp: 1 year |
The Quality Assurance Engineer develops, applies, revises, and maintains quality metrics to support areas of operations at Vivex Biologics, Inc. The role assists in the planning, development, implementation, communication, and maintenance of Vivex’s quality management systems, polices, documentation, data, and customer requirements. The Quality Assurance Engineer is expected to work with all departments to ensure compliance, that the final products are safe, reliable, and effective, and the successful and timely completion of projects. The Quality Assurance Engineer is mainly responsible for the maintenance of CAPA system items. They play a key role in preventing issues or fixing them if they arise by defining, monitoring, and approving the processes needed to achieve production standards. | 09/24/2024 |
| 2449 | Vivex Biologics Miami, FL Operations Processing Technician I Bachelor’s Degree in science or related Exp: 0-1 years |
The Operations Processing Technician I support the processing and documentation requirements of tissue during the cleaning, cutting, shaping, inspecting, and packaging operations for transplantation purposes. The Operations Processing Technician I is also responsible for ensuring that all equipment and supplies used for processing are maintained and ready for use, and that all Processing Room maintenance is completed daily while complying with Quality Assurance requirements as mandated by federal, state, and trade regulations. | 09/24/2024 |
| 2450 | Vivex Biologics Miami, FL Quality Control Labeling Inspector Bachelors Exp: 0-1 years |
The QC Labeling Inspector is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Performs final product labeling and inspections, manages transport and storage of quarantine tissue, and maintains labeling supplies. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Promotes Usage of Problem Solving. Ensure that Labeling Operations are in Compliance with the State and Federal Regulations and AATB Standards. | 09/24/2024 |
| 2451 | Vivex Biologics Miami, FL Inventory Control Coordinator I Bachelors Exp: 0-1 years |
The Inventory Coordinator is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Ensure that Inventory Control Operations are in Compliance with the State and Federal Regulations and AATB Standards. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Resourceful in completing deadlines and can multitask effective. | 09/24/2024 |
| 2452 | Vyriad Rochester, MN Quality Control Analyst Bachelor’s degree in a science related field. Exp: 1 year |
Responsible for performing and validating analytical methods essential for quality control and release of drug product. Performs environmental monitoring of critical manufacturing areas, thus ensuring that manufacturing processes and products meet quality specifications, under moderate direction of managers and senior team members. The analyst shall maintain quality assurance processes, be responsible for testing products, recording, and analyzing data during product development and manufacturing. The analyst will follow through on set processes and ensure adherence to best production practices and product quality standards, as well as monitors the efficiency and cost-effectiveness of product output. Receives general instructions on routine work and detailed instructions on new projects or assignments. | 09/24/2024 |
| 2453 | W. R. Grace & Co. Norco, LA Production Engineer B.S. degree in an Engineering discipline (Chemical Engineering preferred) Exp: 1-5+ years |
Grace is hiring a Production Engineer to join our Norco, LA manufacturing team. The Production Engineer will report to the Engineering Manager and be responsible for monitoring the production processes and ensuring safe and efficient operations to achieve the desired quality and production targets. The successful candidate needs to possess strong communication skills to effectively collaborate with other functional groups. | 09/24/2024 |
| 2454 | W. R. Grace & Co. Columbia, MD Sr Technician Specialist Bachelor’s degree in Science Exp: 1-2 years |
The primary function of this position is to support research activities in the Fluid Catalytic Cracking (FCC) catalyst product line. The typical daily activities of the employee will include: making laboratory/pilot scale preparations of FCC catalyst and additives, submitting samples for analysis and evaluation, keeping detailed records of the work performed, organizing and reporting results, monitoring the quality of the work and assisting in trouble shooting, and performing other assigned duties. Employee will work under general supervision of a research professional and as an integral member of the team. | 09/24/2024 |
| 2455 | W. R. Grace & Co. Baltimore, MD Technician Specialist, FCC BS/BA degree in technical field Exp: 1 year |
Grace is seeking a Technician Specialist to join our FCC Process Technology Team reporting to the FCC Process Tech Lead at the Process Innovation Center in Curtis Bay, Maryland. In this role, you will support Grace’s Special Material Request (SMR) program and assist in making laboratory/pilot scale preparations of FCC catalysts and additives. In the SMR program, an inventory of commercial plant production retains of a variety of grades is maintained and samples are prepared and sent to customers when they request them for exploratory or request for proposal (RFP) testing. Typical activities include drum handling, forklift operation, sample testing, sample packaging and preparing shipping paperwork. When engaged in preparing catalyst typical activities will include operating pilot scale equipment. | 09/24/2024 |
| 2456 | Wave Life Sciences Lexington, MA Scientist I/Scientist II, Pharmacometrics M.S. in clinical pharmacology, pharmacokinetics and metabolism, pharmacometrics, chemical/biomedical engineering, computational biology/chemistry or a Exp: 0-3 years |
Wave Life Sciences is seeking a creative, resourceful, and motivated pharmacometrician to join our organization to assist with and/or lead study design and data analysis for programs at various stages. In this role, you will support programs in the discovery, preclinical, and/or clinical stages spanning multiple modalities including RNA editing, splicing and silencing, as well as several disease areas. Strong communication skills and ability to work cross-functionally in a dynamic, fast-paced environment are required. This position is hybrid, you will be expected to work on site at our Lexington, MA facility. | 09/24/2024 |
| 2457 | Wilmington PharmaTech Newark, DE Research Chemists and Sr. Research Chemists B.A/B.S. or M.A./M.S. in Chemistry or Biochemistry Exp: 0-3 years |
Wilmington PharmaTech (WPT) is seeking self-motivated Research Scientists to join our dynamic chemistry process department for active pharmaceutical ingredient (API) synthesis in clinical phase drug development. | 09/24/2024 |
| 2458 | Worldwide Clinical Trials San Antonio, TX Assistant Clinical Research Coordinator Bachelor’s degree Exp: 1 year |
Clinical Research Coordinator Supervisor, and each clinical trial’s Principal Investigator, is responsible for assisting with assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable. Teamwork and collaboration is paramount, especially as a globally distributed, remote based team. We are at the forefront of Worldwide’s exciting growth and the nexus between candidates and opportunities. | 09/24/2024 |
| 2459 | Worldwide Clinical Trials San Antonio, TX Clinical Research Coordinator 1 Bachelor’s degree Exp: 1 year |
Clinical Research Coordinator and each clinical trial’s Principal Investigator, is responsible for assisting with assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable. Teamwork and collaboration is paramount, especially as a globally distributed, remote based team. We are at the forefront of Worldwide’s exciting growth and the nexus between candidates and opportunities. | 09/24/2024 |
| 2460 | Worldwide Clinical Trials San Antonio, TX Clinical Research Coordinator 1 Bachelor’s degree Exp: 1 year |
Clinical Research Coordinator and each clinical trial’s Principal Investigator, is responsible for assisting with assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable. Teamwork and collaboration is paramount, especially as a globally distributed, remote based team. We are at the forefront of Worldwide’s exciting growth and the nexus between candidates and opportunities. | 09/24/2024 |
| 2461 | HD Biosciences, Inc. (Wuxi) San Diego, CA Research Associate II Bachelors in Biology related field Exp: 1-3 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate II to join the team. | 09/24/2024 |
| 2462 | HD Biosciences, Inc. (Wuxi) San Diego, CA Research Associate I - In Vivo Pharmacology Bachelors in Biology related field preferred Exp: 0-1 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly motivated Research Associate I to support our in vivo pharmacology team for various projects. | 09/24/2024 |
| 2463 | HD Biosciences, Inc. (Wuxi) San Diego, CA Research Associate I Bachelors in Life Sciences or related field preferred Exp: 0-1 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its Discovery Biomarkers team. We’re seeking a highly motivated Research Associate I to support our in vitro/ex vivo immunology team for various projects. | 09/24/2024 |
| 2464 | WuXi AppTec Philadelphia, PA Manufacturing Support Services Associate I Bachelor’s (science preferred) degree Exp: 0-2 years |
Responsible for the support activities and disinfection of GMP space, equipment and associated areas involved in the manufacture of Master and Working Cell Banks, within production facilities involved in the manufacture Cell & Gene Therapy products and final product fills according to current Good Manufacturing Practices (cGMPs). | 09/24/2024 |
| 2465 | WuXi AppTec Marietta, GA Associate Laboratory Technician Bachelor’s Degree Exp: 1 year |
Perform Sterility Testing in compliance with applicable Regulations, International Standards following SOPs in cleanroom type environment, perform QA/QC tasks, prep carts. | 09/24/2024 |
| 2466 | WuXi AppTec Philadelphia, PA Quality Control Environmental Monitoring Associate I Bachelor’s degree with a major in Biology, Microbiology, or related Life Science Exp: 0-3 years |
The Quality Control Environmental Monitoring Associate I is responsible for performing sampling and testing in support of manufacturing and validation activities, under the direction of a Supervisor or higher. Works in a team environment with various laboratory staff. | 09/24/2024 |
| 2467 | WuXi AppTec Philadelphia, PA Manufacturing Associate I - 2nd Shift Bachelor’s (science preferred) degree Exp: 0-2 years |
The Manufacturing Associate I is responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 09/24/2024 |
| 2468 | WuXi Biologics Cranbury, NJ Associate Scientist, QC Testing - Raw Materials & Compendial Bachelor's degree Exp: 1+ years |
The QC Sampler Scientist is responsible for the quality and on-time delivery of samples, EM (Environmental sampling), laboratory inventory management to the various testing sections. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and GMP documentation. | 09/24/2024 |
| 2469 | Xilis Durham, NC Research Associate - Research & Innovation B.S. or M.S. degree in cancer biology, immunology, molecular biology or equivalent Exp: 1+ years |
The candidate will execute critical experiments in the laboratory to nurture and support Xilis' research and development team. Working very closely with thought leaders in immunology, cancer biology, and assay development, the candidate will process samples, gather data, keep meticulous notes, and participate in a detailed analysis, drawing conclusions, and formulation of next steps / experimental designs. The successful candidate will have a strong work ethic and bring exceptional skills to the laboratory with an ability to independently run complex experiments. He or she will have prior experience in primary cell culture, flow cytometry assays, molecular biology techniques, and a demonstrated ability to operate and maintain lab instrumentation and lab automation. Cross-functional team support and communication are central for this position. The candidate will report to the R&D program lead. By joining the team at an early stage, the candidate will have an outsized impact on fundamentally advancing precision cancer care therapy. | 09/24/2024 |
| 2470 | YMC Devens, MA Automation Engineer – Software Bachelor’s Degree in Chemical Engineering or Electrical Engineering preferred Exp: 0-2 years |
Automation Engineer will develop, implement, and test automation/control solutions for our products. This position is customer-driven and focused and is responsible for working with current and potential clients/customers. | 09/24/2024 |
| 2471 | BD Sparks, MD Quality Engineer II (Instrument Plant) MS in Mechanical or Electrical or Industrial Engineering, Biological Sciences, Chemistry, and/or Computer Science or other related field. Exp: 1 year |
The Quality Engineer II is responsible for the application and interpretation of the plant/department procedures to ensure consistency/compliance with Quality Systems. The Quality Engineer II uses the Company Quality Systems to ensure overall compliance and has the knowledge necessary to apply the appropriate statistical and analytical tools. Works with variable enterprise systems/Corporate directives to support new and/or current product lines and processes. Typical assignments may include, supporting one or more instrument platforms on sustaining items such as complaints, non-conformances and day to day issues, supporting audits, actively participating on teams, ensures documentation compliance, processing of CAPAs, change controls, and deviation waivers. Frequent interaction with other functional areas such as Research and Development, Operations, etc. is routine. The Quality Engineer II may take the lead in root cause investigations for issues of moderate complexity. | 09/24/2024 |
| 2472 | BD Covington, GA Lab Technician Bachelor’s degree in Biological Science (microbiology preferred) or related scientific discipline Exp: 1+ years |
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us. | 09/24/2024 |
| 2473 | BD Sparks, MD Quality Engineer II, Chemistry MS in Biological Sciences, Chemistry, Engineering, Computer Science and/or Regulatory Affairs or other related field is required. Exp: No Exp |
The Quality Engineer is responsible for the application and interpretation of the plant/department procedures to ensure consistency/compliance with Quality Systems. The Quality Engineer uses the Company Quality Systems to ensure overall compliance and has the knowledge necessary to apply the appropriate statistical and analytical tools. Works with various enterprise systems/Corporate directives to support new and/or current product lines and processes. Typical assignments may include performing tasks, of moderate complexity, within planned schedules and timelines, test review for ROH release, water testing and OOS support, support for Validations of equipment and test methods, audits, actively participating on teams, ensuring documentation compliance, processing of CAPAs, change controls, and deviation waivers. Frequent interaction with other functional areas such as Research and Development, Operations, Facilities, etc. | 09/24/2024 |
| 2474 | Blue Life Solutions Irvine, CA Entry-Level Microbiology Associate Bachelor’s degree in microbiology, Biology, or a closely related field. Exp: Entry Level |
Blue Life Solutions, LLC is seeking a dedicated and detail-oriented Entry-Level Microbiology Associate to join our dynamic research team. The successful candidate will assist in conducting microbiological experiments, analyzing data, and maintaining laboratory equipment and records. This role offers an excellent opportunity for recent graduates to gain hands-on experience in a collaborative and innovative environment. This position is full time, fixed term (Duration: 2 years, with reevaluation for potential extension). | 09/24/2024 |
| 2475 | Zymo Research Tustin, CA Research Technician I- Epigenetics MS degree or a BS in Molecular Biology, Biochemistry, or related field. Exp: 1 year |
Zymo Research is seeking highly motivated individuals to join our epigenetics R&D team. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. As part of the epigenetics R&D team, you will leverage your skills and familiarity with a range of molecular biology assays, as well as data analysis expertise, to efficiently manage and develop innovative epigenetic and next-generation sequencing (NGS) products. The position is a full-time and fully onsite role based in our Zymo Research facility in Tustin, CA. | 09/24/2024 |
| 2476 | 89bio San Francisco, CA Clinical Trial Associate BA/BS in equivalent field Exp: 1+ years |
Reporting to our Associate Director of Clinical Operations, the Clinical Trial Associate will participate in planning and assisting in the managing the conduct of clinical trials in accordance with company policies and applicable regulations. The role may include some travel when conditions allow. | 09/24/2024 |
| 2477 | Abbott Temecula, CA Associate Engineer Manufacturing Bachelor's degree Exp: 0-2+ years |
Provides support to the Manufacturing organization to facilitate efficient operations within the production area, to optimize existing processes, and to ensure that production goals are met. Monitors performance of manufacturing lines, equipment, machines and tools and corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. Interfaces with Quality and other organizational functions to integrate new products or processes into the existing manufacturing area. | 09/24/2024 |
| 2478 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab, 2nd Shift Science related Bachelor’s Degree Exp: 1 year |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 09/24/2024 |
| 2479 | Abbott Sunnyvale, CA Technical Services Engineer 1 Bachelors Degree - (Preferred Electrical Engineering, Biomedical Engineering ) Exp: 0-2+ years |
Functioning under general supervision, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and various departments through consultation. Requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. | 09/24/2024 |
| 2480 | Abbott Sylmar, CA Technical Services Engineer I Bachelors Degree - (Preferred Electrical Engineering, Biomedical Engineering ) Exp: 0-2+ years |
Functioning under general supervision, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and various departments through consultation. Requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. | 09/24/2024 |
| 2481 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab, 3rd Shift Science related Bachelor’s Degree Exp: 1 year |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 09/24/2024 |
| 2482 | AbbVie North Chicago, IL Associate Scientist II Master’s Degree Exp: No Exp |
The Analytical Development group is responsible for programs that are transitioning from development stage to optimization and commercialization. We lead final method development, optimization, and validation, ensuring all analytical methods are fit for use in commercial QC laboratories. Key deliverables include product control strategies informed by analytical data and method understanding; robust analytical methods suitable for commercial QC labs; comprehensive data packages that drive product and process understanding; stability studies to establish commercial product dating; and approvable marketing application submission content. This position will work primarily inside of the laboratory, providing testing support to meet Analytical Development’s deliverables for pipeline programs. | 09/24/2024 |
| 2483 | AbbVie North Chicago, IL R&D Technician III BS Exp: 1+ year |
The R&D Technician carries out daily activities in the vivarium and will need to be proficient in humane rodent and dog handling skills, dosing by oral gavage, intravenous, and intraperitoneal routes, bleeding from the tail vein, assessing health, and performing humane euthanasia. The ideal candidate will also have postmortem examination (necropsy) experience. There are opportunities for expanding the candidate’s responsibilities beyond those identified as core job responsibilities. At all times, the candidate must adhere to the highest standards of animal welfare and personal conduct consistent with Abbvie values. The candidate will also be required to utilize a computer system to record all activities and observations. Ability to design, plan, organize and implement tasks within an allotted timeframe. Basic competence of Excel Spreadsheets, word processing, and email and knowledge of computerized maintenance management systems. The candidate will be required to work with potentially hazardous compounds, using appropriate precautions for the safety of the candidate and co-workers, and to prepare dosing formulations. | 09/24/2024 |
| 2484 | AbbVie North Chicago, IL Associate Scientist II, Analytical Chemistry Master’s Degree Exp: No Exp |
Within Small Molecule Chemistry and Manufacturing Control (CMC) Development, Analytical Research & Development focuses on utilizing measurement scientists of analytical chemistry to inform the development of new chemical entities and the associated formulations dosed in a preclinical and clinical setting across a wide range of pipeline programs. The group is highly cross-functional and works closely with internal Analytical R&D colleagues as well as colleagues within Discovery, Process Chemistry, Pharmaceutics and Drug Product Development. | 09/24/2024 |
| 2485 | AbbVie Irvine, CA Associate Scientist II, Pharmacology Master’s Degree Exp: 0+ years |
The Neurotoxin Research Group at Allergan/AbbVie is seeking a highly motivated and independent Associate Scientist II to join our Toxin Innovation Pharmacology Group. This individual will execute in vivo neuromuscular and sensory pharmacology studies, contributing to the design, execution, and communication of novel research in our highly collaborative neurotoxin discovery and innovation program. The successful candidate for this position will contribute to projects aimed at in vivo pharmacological characterization of biotherapeutics. He/she/they will be required to work on a variety of in vivo pharmacology models to help characterize and evaluate biological compounds. The successful candidate will organize, analyze, and interpret results, come forward with recommendations, and present the findings to senior personnel or in team meetings. Experience with rodent models is required. A background in neurobiology is highly desirable, but not required. | 09/24/2024 |
| 2486 | AbbVie North Chicago, IL Associate Scientist II or Scientist I - Process Chemistry Master’s Degree Exp: 0+ years |
Process Research and Development is responsible for inventing and executing the chemical processes and preparing active pharmaceutical ingredient (API) to enable clinical trials, toxicology studies and drug product development for Abbvie’s pre-clinical and clinical candidates. We create valuable intellectual property through composition of matter, chemical processes, and technology resulting in a cost-effective commercial manufacturing process. We develop the supply chain for APIs, prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We seek a highly motivated scientist with strong synthetic skills to work under the mentorship of a supervisor and to work in a multi-functional team environment. Opportunities may also exist to contribute to high-throughput experimentation, automation, and data science. | 09/24/2024 |
| 2487 | Tome Biosciences Watertown, MA Senior Research Associate, Analytical Development BS/MS in engineering, chemistry, biology, or other relevant degree Exp: 1-3 years |
Our Analytical Team is growing! Reporting to our Senior Scientist, Analytical Development, we are seeking a Senior Research Associate, Analytical Development to join our organization. In this role, the individual will perform various assays to analyze quality attributes of our lipid nanoparticles (LNPs), oligonucleotides and mRNA, with a focus on biophysical techniques. The individual will also contribute to method development to advance our knowledge in product attributes of these components. | 09/18/2024 |
| 2488 | Transpire Bio Miami, FL Associate Scientist I BSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct basic laboratory activities including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Set up and operate lab equipment. Prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all tests performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine. calculations. Support the manufacture of inhalation drug products. Prepare samples for blend uniformity as required. Participate in project team activities and support project timelines and proactively contribute to meeting team objectives. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate health & safety rules and procedures. Comply with Corporate guidelines and policies. | 09/18/2024 |
| 2489 | Transpire Bio Miami, FL Associate Scientist II MSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct basic laboratory activities including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Set up and operate lab equipment. Prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all tests performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine. calculations. Support the manufacture of inhalation drug products. Prepare samples for blend uniformity as required. Participate in project team activities and support project timelines and proactively contribute to meeting team objectives. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate health & safety rules and procedures. Comply with Corporate guidelines and policies. | 09/18/2024 |
| 2490 | TScan Therapeutics Waltham, MA Senior/Principal Research Associate, New Technology & Product Development M.S. in biology, immunology, pharmacology, or related field. Exp: 0-2+ years |
TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for an experienced researcher to join our team as Senior/Principal Research Associate, supporting the New Technology and Product Development Team. The incoming candidate will have the opportunity to work at the intersection of biology and engineering to develop the next generation of TCR-T cell products. The ideal candidate should have relevant experience in T cell immunology, primary and tumor cell culture, cell-based assays, and flow cytometry, and enjoy exciting, collaborative and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 09/18/2024 |
| 2491 | Twist Bioscience South SF, CA Manufacturing Associate II, Library Production Bachelor in biology, chemistry, biochemistry, or similar disciplines preferred Exp: 1-3 years |
We are looking for an outstanding Manufacturing Associate II to join our Operations Team in South San Francisco, CA. The Manufacturing Associate II will produce a variety of DNA-based products with a focus on molecular biology techniques to meet production forecast and timelines and will assist research personnel with technology transfer to production. The candidate will be highly motivated, organized, willing to take initiative, and desire work in a highly collaborative environment. The ideal candidate will be eager to learn new techniques, have excellent molecular biology knowledge and skills, take detailed experimental notes, and communicate effectively with peers and management. | 09/18/2024 |
| 2492 | Twist Bioscience South SF, CA Sr Research Associate Bachelor’s or Master’s degree in Molecular Biology, Chemical Engineering, Biochemistry, Chemistry or closely-related field. Exp: 1-3 years |
We are seeking an outstanding Senior Research Associate to join our R&D team. The successful candidate will support R&D efforts in developing innovative nucleic acid-based applications and tools for synthetic biology and NGS products. This position will involve performing a range of experiments focused on development of protein expression and enzyme purification platforms. The ideal candidate will be very organized, have excellent molecular biology knowledge and laboratory skills, and communicate effectively with colleagues. | 09/18/2024 |
| 2493 | Unither Rochester, NY QA Operations Documentation Specialist BS degree in Life Sciences, Communications, Business Administration, Technical Writing, or related field is preferred. Exp: 1-3 years |
The QA Operations Documentation Specialist position provides documentation support aligned with commercial and development production. This position interacts with cross functional departments throughout the site to ensure all cGMP documentation is ready in advance of the schedule. The QA Operations Documentation Specialist is responsible for ensuring all necessary instructions and associated documentation is printed, verified and provided to the operations team. This position is also responsible for ensuring completed batch documentation is scanned into the system and sent to the customers. | 09/18/2024 |
| 2494 | Unither Rochester, NY Validation Specialist Bachelor’s Degree in Science or Engineering Discipline preferred. Exp: 0-2 years |
Manages validation projects or multiple validation project activities under limited supervision and performs assigned validation tasks such as validation product annual reviews and validated utilities re-certifications. | 09/18/2024 |
| 2495 | Astellas Pharma Seattle, WA Research Associate II MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Cell Analytics, Core Technology Department. This individual will contribute to the characterization of our gene edited Universal Donor Cells, by utilizing various cell culture techniques. They will work as a key member on a fast-paced team to culture pluripotent stem cells as well as run cellular assays to characterize our proprietary Universal Donor Cells. | 09/18/2024 |
| 2496 | Vala Sciences San Diego, CA Research Associate (RA)/Senior Research Associate (SRA) – iPSC Manufacturing B.S. or M.S. in Cell/Molecular Biology, Biochemistry, Neuroscience, or related field Exp: 1-2 years |
We’re seeking an RA or SRA to join our dynamic induced pluripotent stem cell (iPSC) research and manufacturing program. The successful candidate will manage iPSC lines and their differentiation to different cell types, like cardiomyocytes, microglia, neurons, and astrocytes. These differentiated iPSC lines will be used for internal R&D projects, commercial research contracts, and manufacture for sale. You will evaluate and validate differentiated cell lines with biomarker detection methods like ICC or flow cytometry, and investigate and characterize cellular function using Vala’s live-cell fluorescent imaging technology. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve | 09/18/2024 |
| 2497 | Vala Sciences San Diego, CA Research Associate (RA)/Senior Research Associate (SRA) – Assay Development and iPSC Maintenance B.S. or M.S. in Molecular/Cell Biology, Biochemistry, Neuroscience, Bioengineering, or related Exp: 1+ years |
We’re seeking an RA or SRA to join our dynamic assay development and induced pluripotent stem cell (iPSC) research team. The successful candidate will execute validated assays for contract research projects and assist in management and maintenance of iPSC lines. Additionally, you will work with senior scientists in the Neurobiology and Cardiology groups to plan and perform experiments for assay development to support Vala’s internal and contract research projects. You will maintain differentiated iPSC cell cultures for live cell assays using Vala’s Kinetic Image Cytometry (KIC) technology, as well as perform IF staining to assist in development of reproducible and optimized assays. You may perform differentiation of iPSC to different cell types, such as neurons, astrocytes, microglia and cardiomyocytes. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 09/18/2024 |
| 2498 | Beckman Coulter Life Sciences Remote - Chicago, IL Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 2499 | Beckman Coulter Life Sciences Remote - Southern, IL Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 2500 | Beckman Coulter Life Sciences Remote - Milwaukee, WI Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 2501 | Beckman Coulter Life Sciences Remote - St. Louis, MO Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 2502 | Vantage MedTech Lenexa, KS Process Engineer BS or MS degree in Engineering, preferably Mechanical or Manufacturing Engineering Exp: 1-3 years |
The Process Engineer will be responsible for ensuring that our innovative designs are transitioned into effective and sustainable production. Our life saving products are manufactured in Kansas City and require predictable delivery of high quality, cost-effective production over 5+ year product lifetimes. You will collaborate with Vantage MedTech’s Engineering and Manufacturing teams to provide input on the device design’s manufacturability, and plan and execute the transfer of these new products to our manufacturing facility. You will be responsible for ensuring that robust manufacturing processes are created, updated and in compliance with company standards, ISO and GMP as required. In addition, you will help drive improvement projects that impact quality and productivity. | 09/18/2024 |
| 2503 | Varian San Jose, CA Quality Incoming Inspections Engineer (Metrology Engineer) Master’s Degree Exp: 1 year |
As Quality Incoming Inspections Engineer you are expected to be able to perform assignments independently by applying Good Manufacturing Practices in all areas of responsibility to ensure our customers receive the highest possible quality products. This position is responsible for Incoming Inspection activities, interactions with internal customers to ensure parts are inspected in a timely manner in a FDA 21 QSR 820 and ISO 13485 regulated environment. You will need to perform all assigned duties and conduct business in a professional manner. | 09/18/2024 |
| 2504 | Variantyx Framingham, MA Analysis Preparation Scientist BS/BSc in a relevant field (Biology, Genetics) Exp: 1 year |
As a full time Analysis Preparation Scientist located in the US you will be responsible for the pre-interpretation step in our analysis process. | 09/18/2024 |
| 2505 | Vaxcyte San Carlos, CA Associate Scientist II, Analytical Development MS in Chemistry, Analytical Chemistry preferred, Organic / Biochemistry Exp: 1-4 years |
Looking for an energetic and talented individual to join our Analytical Development team. Primary responsibility for the incumbent will be to support the developmental activities currently on going in the laboratory as assigned. | 09/18/2024 |
| 2506 | Vector Laboratories Newark, CA Manufacturing Associate II, Library Production BS or BA degree in Chemistry Exp: 0-3 years |
The Manufacturing Associate I is primarily responsible for manufacturing Vector’s products according to established procedures and documenting all work in production batch records using established good documentation practices. The Manufacturing Associate I will operate and maintain common laboratory equipment as per instructions and works under general supervision on assigned tasks. Technical expertise should include strong knowledge of general laboratory safety and practices, basic knowledge of modern synthetic organic chemistry, multistep synthesis, and purification technique. This position will report to the Site Leader. | 09/18/2024 |
| 2507 | Adamson Analytical Laboratories Corona, CA Microbiology Laboratory Technician B.S. in Biology Exp: New Grads are welcome |
We are hiring for a Microbiology Lab Technician to join our Corona, CA team; Our ideal candidate will exhibit a passion for exploration and possess an insatiable curiosity! | 09/18/2024 |
| 2508 | Velocity Clinical Research Union, SC Clinical Research Coordinator I Bachelor’s degree in Science or Engineering Discipline preferred. Exp: 1 year |
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. | 09/18/2024 |
| 2509 | Velocity Clinical Research Albuquerque, TX Clinical Research Coordinator I Bachelor’s degree in Science or Engineering Discipline preferred. Exp: 1 year |
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. | 09/18/2024 |
| 2510 | Veloxity Labs Peoria, IL Associate Scientist II Bachelor’s degree in science (chemistry/biochemistry preferred) Exp: 1-2 years |
As an Associate Scientist II, you will be using state-of-the art technologies to perform bioanalytical testing for emerging pharmaceutical and biopharma companies. At Veloxity, we hire driven and motivated individuals and provide training and career advancement opportunities within our organization. | 09/18/2024 |
| 2511 | Veranova Devens, MA Senior Analytical Chemist BS in Chemistry Exp: 1-3 years |
The Senior Analytical Chemist is responsible for all project activities in ARD, including sample analyses and method development, transfer, and validation in a safe and reliable manner. This position requires the application of basic chemistry knowledge, as well as standard laboratory techniques and procedures. The Senior Analytical Chemist must also be able to make keen observations and learn how to solve more complex technical issues. | 09/18/2024 |
| 2512 | Veranova West Deptford, NJ Quality Control Chemist - Night Shift Bachelor's Degree in Chemistry or related field Exp: 1 year |
The purpose of the Quality Control Chemist is to perform chemical testing of in-process, raw materials, intermediates, and finished product samples in support of GMP production and stability testing. They execute standard analyses with regular supervision. | 09/18/2024 |
| 2513 | Veranova Devens, MA Analytical Scientist MS in Analytical Chemistry or equivalent Exp: 1 year |
Responsible for the design, development, qualification, validation, and implementation of analytical procedures in support of research, GMP production, and stability testing. The Analytical Scientist is expected to provide quality ideas and contribution to the assigned challenges; mentors junior analysts and offers recommendations and knowledge to other Veranova staff. | 09/18/2024 |
| 2514 | Veranova West Deptford, NJ Project Engineer Bachelor’s degree in chemical or mechanical engineering or equivalent degree required Exp: 1-5 years |
The Project Engineer is responsible for the safe and effective development, design, and implementation of assigned capital projects that are completed on time, on or below budget, with an end result that is fit for its intended purpose. Essential considerations are given to safety, quality, operability, processing efficiency, maintainability, and environmental compliance. The Project Engineer will also include participation in troubleshooting efforts, operation process support and continuous improvement. | 09/18/2024 |
| 2515 | Vericel Corporation Cambridge, MA Associate I, Cell Therapy Manufacturing Bachelor’s or higher degree (Life Sciences or related field) Exp: 0-2+ years |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. | 09/18/2024 |
| 2516 | Vericel Corporation Cambridge, MA Associate II, Cell Therapy Manufacturing Bachelor’s or higher degree (Life Sciences or related field) Exp: 1-2 years |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. | 09/18/2024 |
| 2517 | Vertex Pharmaceuticals San Diego, CA Molecular & Cell Biology Senior Research Associate Masters Degree (or equivalent degree) in biological science Exp: 0-2 years |
Join the cutting-edge team at Vertex Pharmaceuticals as a Senior Research Associate for Cell Biology in our Tissue Dissection Group. Our Molecular & Cell Biology (MCB) group in San Diego is seeking an outstanding Senior Research Associate to work in our tissue dissection function to generate high quality cells from primary human tissues for numerous Vertex research programs.The ideal candidate will have experience in human tissue dissection (especially DRG, lung, kidney & liver). This role will require the candidate to be reliable & flexible as donated tissues will require processing out-with normal working hours and during weekends. The ideal candidate will have the ability to drive method development & process optimization of dissection workflows. Familiarity with histological grossing & processing of tissues is a plus. | 09/18/2024 |
| 2518 | Vertex Pharmaceuticals Boston, MA Process Development Engineering Senior Scientific Associate Master’s degree in Biochemistry, Engineering, Biology or related discipline Exp: 0-2 years |
Vertex is seeking a talented Process Development Engineering Senior Scientific Associate to join our Process Development team. This individual will support the media development projects in cell and gene therapy applications, through a combined approach of fundamental hypotheses and high throughput screening and optimization. | 09/18/2024 |
| 2519 | Vertex Pharmaceuticals Boston, MA Pathology Senior Research Associate Master’s Degree in Biological Sciences or equivalent Exp: 0-2 years |
Preclinical Safety Assessment (PSA) is a global function responsible for the design and conduct of comprehensive nonclinical safety programs. Its pathology team supports animal model development and efficacy at all stages of discovery for the evaluation of candidate therapeutic agents. We are seeking a Senior Research Associate to perform histology techniques, data acquisition and compilation using state-of-the-art molecular pathology techniques to join our (PSA) team at Vertex. The incumbent will interface closely with other scientists, veterinary pathologists and histotechnologists in PSA as well as other cross-functional project teams to provide timely, high-quality data to support multiple projects across our drug development pipeline. | 09/18/2024 |
| 2520 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist I BA/BS Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 09/18/2024 |
| 2521 | Sovereign Pharmaceuticals Fort Worth, TX QC Lab Technician BA/BS Chemistry Exp: 1-2 years |
Supporting QC Laboratory operations by performing, Documentation - most activities require proper documentation, Flexibility in prioritization of duties to ensure the QC Laboratory serves its internal and external customers | 09/18/2024 |
| 2522 | VGXI Conroe, TX Process Development Technician Bachelor’s degree Exp: 1-3 years |
Conduct research scale production of plasmid DNA on an ongoing basis. Perform and document routine maintenance on PD equipment. Assist the execution and analysis of data for the purpose of fermentation and purification process development. Assist the analysis of samples from cGMP seed banking, fermentation and purification processes. Assist experiments to evaluate new technologies as designed and supervised by senior team members. Maintain a clean and organized laboratory environment. | 09/18/2024 |
| 2523 | VIATRIS St. Albans, VT Chemist – 2nd Shift Bachelor’s degree Exp: 0-2 years |
Performs and documents the analysis of samples following approved test methods. Calculate, check, and/or review data. Assist with method development, validation, and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 09/18/2024 |
| 2524 | VIATRIS Morgantown, WV Associate - LIMS Bachelor’s degree Exp: 0-2 years |
Provide Tier 1 support to the laboratory including answering questions and providing technical support to management and laboratory personnel as necessary. Assist with preparing LIMS stability studies for all incoming new product set downs, including both release and process validation samples. Assist with creation of LIMS Product Specifications, Item Codes, and related LIMS components for all new products. Assist with revising LIMS Product Specifications, Item Codes, and related LIMS components for all Specification changes. Apply LIMS Product Specification changes to existing samples in the Research and Development Chemistry laboratory. Assist with Stability Management duties as assigned | 09/18/2024 |
| 2525 | VIATRIS St. Albans, VT Chemist – 2nd Shift Bachelor’s degree Exp: 0-2 years |
Performs and documents the analysis of samples following approved test methods. Calculate, check, and/or review data. Assist with method development, validation, and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 09/18/2024 |
| 2526 | VIATRIS Greensboro, NC Quality Compliance Associate Bachelor's degree Exp: 1-2 years |
Support the coordination, completion and documentation of site incident, investigation, complaint, and CAPA records to ensure timely closure of associated activities. Support the activities associated with the site’s data integrity document control and disposition activities. Support the operations related to the performance of the site internal inspection program. Review and/or revise SOPs and Work Instructions as they relate to internal and/or external inspections and incidents and investigations. Collect and report metrics associated with inspections and incident investigations for site Quality Council. Provide quality support during audits and inspections performed by customers, health authorities and/or regulatory agencies. | 09/18/2024 |
| 2527 | Stryker Remote, Customized Implant Design Engineer Bachelor of Science in Engineering, Mechanical Engineering, or Biomedical Engineering Exp: 0+ years |
Stryker is seeking to hire a Design Engineer to support Stryker Craniomaxillofacial (CMF) Division. This role has a direct impact on healthcare by designing customized patient implants. This is a remote role supporting the West Coast, and it requires working standard business hours in either the Pacific or Mountain Time Zone. | 09/11/2024 |
| 2528 | Sun Pharma Billerica, MA Microbiology Analyst I BS in Microbiology or relevant experience Exp: 0-2 years |
Performs GMP testing of raw materials, in-process and finished products, stability samples, and non-routine sample analyses per established procedures and methodology. | 09/11/2024 |
| 2529 | Sunbird Bio Cambridge, MA Research Associate BS or MS in biology, chemistry, biochemistry, or biomedical/chemical engineering or similar discipline Exp: 1-3+ years |
The Product Development team at Sunbird Bio's U.S. headquarters in Cambridge, Massachusetts, is searching for an innovative, motivated, and inquisitive Research Associate to help advance our neurodegenerative disease programs along the development pipeline. The ideal candidate will leverage their technical immunoassay experience to discover new biomarkers to further understand neurodegenerative disease signatures in blood samples. | 09/11/2024 |
| 2530 | BioDuro-Sundia Irvine, CA Scientist I, Formulation Development MS in Chemistry or related scientific discipline Exp: 1+ years |
The Scientist I, Formulation Development, assists in the design and development of drug delivery systems and dosage forms. | 09/11/2024 |
| 2531 | Sunflower Therapeutics Medford, MA Bioprocess Engineer Bachelor’s degree in chemical engineering or equivalent Exp: 1-3 years |
Sunflower Therapeutics is recruiting a motivated and highly organized individual to support its mission to deliver protein manufacturing solutions that anyone can use to create innovative new medicines, food products, and other bio-based products. Sunflower is advancing “right-sized” and ecient approaches to democratize protein manufacturing using strain engineering, integrated process development, and automated small-footprint facilities Reporting to the Director of Engineering Operations, the Bioprocess Engineer will be responsible for supporting engineering operations at Sunflower Therapeutics to enable the advancement of Sunflower’s protein manufacturing equipment prototypes. This individual will assist in the design, development, testing, and implementation of biomanufacturing systems for recombinant proteins. A successful candidate will be able to utilize bioprocess data to interpret product and process requirements and ensure the hardware design meets specified and operational standards. This individual will diagnose technical problems across system functions and suggest and carry out creative and timely solutions. As Sunflower grows, the Bioprocess Engineer will contribute to the continuous improvement of Sunflower’s automated multi-product protein manufacturing systems. | 09/11/2024 |
| 2532 | Adamson Analytical Laboratories Corona, CA Microbiology Laboratory Technician B.S. in Biology Exp: Entry Level, New Grads |
We are hiring now for a Microbiology Lab Technician to join our Corona, CA team; Our ideal candidate will exhibit a passion for exploration and possess an insatiable curiosity! | 09/11/2024 |
| 2533 | Synaptive Medical San Francisco, CA Clinical Applications Specialist Bachelor of Science degree Exp: 1-3 years |
The Clinical Applications Specialist (CAS) is an essential part of Synaptive Medical. The CAS provides primary on-site clinical support of Synaptive’s surgical technologies by acting as a knowledgeable and highly skilled technical resource in the hospital operating room. The CAS is expected to actively manage primary accounts assigned to them while also contributing to regional and national coverage as needed. At their assigned accounts, the CAS is responsible for driving customer engagement, supporting commercial success, pursuing excellence in clinical support, developing themself and the team, and maintaining good corporate citizenship. | 09/11/2024 |
| 2534 | Synaptive Medical Chicago, IL Clinical Applications Specialist Bachelor of Science degree Exp: 1-3 years |
The Clinical Applications Specialist (CAS) is an essential part of Synaptive Medical. The CAS provides primary on-site clinical support of Synaptive’s surgical technologies by acting as a knowledgeable and highly skilled technical resource in the hospital operating room. The CAS is expected to actively manage primary accounts assigned to them while also contributing to regional and national coverage as needed. At their assigned accounts, the CAS is responsible for driving customer engagement, supporting commercial success, pursuing excellence in clinical support, developing themself and the team, and maintaining good corporate citizenship. | 09/11/2024 |
| 2535 | SystImmune Redmond, WA Research Associate/Senior Research Associate BS or MS in immunology, biochemistry, molecular biology, structural biology, or a related field. Exp: 1+ years |
We are seeking a skilled Research Associate/Senior Research Associate with experience in utilizing display technologies (yeast/phage) in protein engineering, directed evolution, or binder discovery. This is a laboratory-based role that will be supporting protein engineering efforts in discovering novel binders and novel protein leads/scaffolds. The position will join a growing protein engineering team in an innovative organization and reports to the Director of Protein Engineering. The ideal candidate will be a quick learner with a broad experience set with direct expertise in a display technology and/or an adjacent field including but not limited to high throughput molecular biology, antibody/binder discovery, and protein engineering. Industry experience in biologics drug development is required. | 09/11/2024 |
| 2536 | Taconic Biosciences Rensselaer, NY Senior Lab Specialist Environmental Monitoring & Microbiology Bachelor’s degree within a science discipline Exp: 1 year |
If you ever wondered what is living on a door handle or if the hotel hot tub is full of bacteria, this opportunity may be the right one for you! We’re looking for a dedicated, motivated, and creative person who can help us carry out our mission: to create innovative solutions that both progress medical research and maintain the highest standards of laboratory animal care. The Senior Lab Specialist, Environmental Monitoring & Microbiology will be responsible for routine lot release testing, microbial evaluation of health and quality control samples as well as screening of various raw materials. Responsibilities also include data entry for lot releases and accessioning of test samples. This individual will also be the primary back-up for the Environmental Monitoring technician, whose responsibilities include scheduling, sample collection, sample analysis, microbial identification, data entry, and data review. This position is responsible and accountable for the accuracy of test results. | 09/11/2024 |
| 2537 | Taconic Biosciences Rensselaer, NY Senior Laboratory Specialist Molecular Analysis - 1st and 2nd Shift Bachelor’s Degree from a four-year college Exp: 1 year |
The Senior Laboratory Specialist performs a variety of molecular assays on animal samples and must be able to generate high-quality results in a timely manner. This individual should be comfortable working in a high-throughput environment and be able to use proper judgement to make technical decisions on assay performance issues. | 09/11/2024 |
| 2538 | Tactiva Therapeutics Buffalo, NY Senior laboratory technician Master's or Bachelor's Degree Exp: Master's: 18 months; Bachelor's: 30 months |
The senior laboratory technician performs specialized, technical scientific duties unique to research and development (R&D) for Tactiva Therapeutics. The senior laboratory technician designs and optimizes assay processes including sample preparation, workflow automation, and analytic detection, as well as provides data for critical review of test development. The senior laboratory technician provides direct scientific and analytic support to the laboratory director(s) and monitors timelines to meet production goals and objectives. | 09/11/2024 |
| 2539 | Takeda Boston, MA Associate Product Manager / Product Manager, Shared Platforms & Services BS/BEng in a technically relevant field of study (e.g. Engineering, Information Technology, Computer Science, Computer Engineering) Exp: 1-3 years |
Are you looking for a patient-focused, innovation-driven company that will inspire and empower you to shine? Join us as a Product Manager on the Shared Platforms & Services Team in Takeda’s Global Data, Digital, and Technology (GDD&T) team based in Cambridge, Massachusetts. The Shared Platforms & Services Team is a global team that allows Takeda to design, develop, and deploy externally facing digital solutions to patients and healthcare professionals (HCPs). Our team of software engineers and IT professionals share a passion for building trail-blazing digital solutions, while ensuring quality and compliance are followed to the highest standards. Our team works closely with local business teams, commercial, drug product teams, and research & development as key compliance enablers for both internal and external partners developing digital health solutions. The Product Manager will own the vision and product strategy for an internally facing compliance platform and the administration of Takeda’s digital asset compliance process framework. | 09/11/2024 |
| 2540 | Takeda Boston, MA Cell Therapy Data Engineer Master’s degree in Information Technology, Information Systems, Data Analytics, Engineering, Computer Science, or related field Exp: 1 year |
Takeda Development Center Americas, Inc. is seeking a Cell Therapy Data Engineer in Cambridge, MA with the following requirements: Master’s degree in Information Technology, Information Systems, Data Analytics, Engineering, Computer Science, or related field plus 1 year of related experience. Prior experience must include: Utilize computing languages including R, C/C++, Python, and Java; Apply knowledge in distributed computing, databases (e.g., SQL), relational databases (e.g., PostgreSQL), and Amazon Web Services; Demonstrate experience in database programming and development of dashboards; Demonstrate experience in data integration, programming, and the objective evaluation & utilization of analytical tools & libraries. | 09/11/2024 |
| 2541 | Takeda Social Circle, GA Sr QA Technician Bachelor's degree in scientific discipline Exp: No exp |
As the Sr QA Technician, you will be responsible for inspection of production materials, components, and chemicals to the Manufacturing facility. You will identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Takeda Quality practices. You will demonstrate effectiveness in task completion, decision-making and handling multiple projects. The hours of this position are 12PM-8:30PM, Monday-Friday; weekend and holiday work. Overtime may be required. | 09/11/2024 |
| 2542 | Takeda Boston, MA Senior Research Associate I, IVS Imaging Technician MS in a scientific discipline (or equivalent) Exp: 1+ years |
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Research Associate I, IVS Imaging Technician in our Cambridge, MA location. As a Senior Research Associate I, IVS Imaging Technician, you will perform complex animal manipulations for imaging procedures, supporting multiple therapeutic areas of the Company including Oncology, Drug Metabolism and Pharmacokinetics, CNS, GI and Imaging. You will also perform advanced dosing and biomethodology, sample collection, and animal procedures with efficiency, accuracy and attention to detail. As part of the Comparative Medicine team, you will report to Associate Director, Comparative Medicine and work with other groups within Preclinical and Translational Sciences. | 09/11/2024 |
| 2543 | Takeda Boston, MA Research Senior Associate, IBD/GI MS in a scientific discipline (or equivalent) Exp: 1+ years |
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Research Senior Associate, IBD/GI, Inflammation Research where you will e part of a team focused on validation of novel targets and the evaluation of drug candidates for the treatment of chronic fibroinflammatory diseases. | 09/11/2024 |
| 2544 | Tanvex San Diego, CA QC Associate I, Lab Control BS in chemistry, biology, biochemistry or related life sciences discipline. Exp: 0-3 years |
The Quality Control Associate I, Lab Control is responsible for supporting the control and management of samples within QC and performing routine testing of in-process, release, and stability samples following written methods and procedures. The position will work as part of the Analytical Development (AD) / Quality Control (QC) group to support the team responsibilities. Adherence to GMP/ GDP guidelines and ability to follow SOP’s is required. | 09/11/2024 |
| 2545 | Tanvex San Diego, CA Manufacturing Associate, Upstream Bachelor's in life sciences or related discipline Exp: 0-3 years |
Under supervision, the Manufacturing Associate, Upstream, will perform routine manufacturing activities in GMP manufacturing areas including fermentation and/or cell culture, and the associated sub-processes/preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Perform manufacturing steps, execute routine batch records, and revise documents such as batch records and SOPs as needed. Flexible shift schedule and overtime may be required. | 09/11/2024 |
| 2546 | Tanvex San Diego, CA Manufacturing Associate, Downstream Bachelor's in life sciences or related discipline Exp: 0-3 years |
Under general supervision, the Manufacturing Associate, Downstream, will perform routine manufacturing activities in GMP manufacturing areas including purification and the associated sub-processes/ preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Perform manufacturing steps, execute routine batch records, and revise documents such as batch records and SOPs as needed. Flexible shift schedules and overtime may be required. | 09/11/2024 |
| 2547 | TE Connectivity Middletown, PA Technician IV Bachelor degree in related discipline Exp: 1-5 years |
The Appliances business is seeking to fulfill an engineering technician position to support engineering initiatives within the Appliance BU. The engineering technician will be primarily responsible supporting sample creation at the Middletown On-Wire lab. This position will require close coordination with our TE Engineering, Sales, and Product management teams to support new product development and expand sales. Other activities include and supporting the local engineering team with sample preparation, testing and analysis, fixture design, and shipping. | 09/11/2024 |
| 2548 | TE Connectivity Middletown, PA R&D Product Development Engineering BA/BS or MA/MS? Degree in ?Mechanical Engineering? or ?Electrical Engineering Exp: Entry Level, New Grads |
At TE Connectivity, you’ll help bring our purpose to life by creating a safer, sustainable, productive and connected future. In your role as a R&D Product Development Engineer in the Appliances Business Unit, you will help us make the connections that move the world forward by: Taking responsibility for supporting the development of new electrical connectors for the home appliances industry. Collaborating with senior engineers to collect requirements from customers, develop new concepts using 3D & 2D CAD, build prototypes, establish testing and validation plans, and work with operations to build tooling for mass production. | 09/11/2024 |
| 2549 | TE Connectivity Landisville, PA Controls Engineer Bachelor’s degree in electrical or mechanical engineering Exp: 0-3 years |
The focus of this position is to install machine safeguarding and control reliability safety systems on existing equipment. The ideal candidate will complete a quantitative risk assessment for manufacturing equipment and develop corrective actions that isolate the point-of-operation hazards and provide ISO category 3 safety circuit integrity. Secondary job duties include troubleshooting automated equipment involving programmable logic controllers, robotics, vision systems, pneumatics, and electrical instrumentations. | 09/11/2024 |
| 2550 | Tempus Durham, NC Molecular Technologist - Lead Trainer MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. Work closely with the Training Supervisor to schedule and execute training sessions with molecular team members according to the defined schedule. Routinely update checklists with training status, i.e. scheduled date of training, completion date of observations, side-by-sides, and competency assessments. Tailor training plans to individual team members, as appropriate, to ensure competency and confidence prior to initiation of clinical testing. Request competency modules in MediaLab and ensure completion and submissions per defined timelines. Review and update training materials, as needed. | 09/11/2024 |
| 2551 | Tempus Atlanta, GA Molecular Technologist I-IV BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 0-2 years |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2552 | Tempus Chicago, IL Operations Specialist, Biological Modeling Lab Bachelors in Biological Sciences or Engineering. Exp: 1-3 years |
Tempus Biological Modeling is building the world's largest patient-derived organoid library to evaluate real-world data observations by constructing large scale data sets of molecular and experimental data. Tempus Biological Modeling is actively engaging with academic and industry partners in life science research, and we seek an Operations Specialist to accelerate our laboratory operations and academic research partnerships. | 09/11/2024 |
| 2553 | Tempus Chicago, IL Molecular Technologist (relocation assistance) BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2554 | Tempus Chicago, IL Molecular Technologist I BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2555 | Tempus Raleigh-Durham, NC Molecular Technologist I-IV: Sunday-Wednesday, AM Shift BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2556 | Tempus Raleigh-Durham, NC Molecular Technologist I-IV: Wednesday-Saturday, 2pm Shift BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2557 | Tessera Somerville, MA Engineer I/II, LNP Process Development Bachelor's or Master's degree in Chemical Engineering, Bioengineering, or Biological Sciences Exp: Bachelor's: 0-4 years; Master's: 0-2 years |
Tessera Therapeutics is pioneering Gene Writing™— a new biotechnology designed to offer scientists and clinicians the ability to write small and large therapeutic messages into the genome, thereby curing diseases at their source. Gene Writing holds the potential to become a new category in genetic medicine, building upon recent breakthroughs in gene therapy and gene editing while eliminating important limitations in their reach, utilization, and efficacy. Tessera Therapeutics was founded by Flagship Pioneering, a life sciences innovation enterprise that conceives, resources, and develops first-in-category companies to transform human health and sustainability. | 09/11/2024 |
| 2558 | Teva Pharmaceuticals Davie, FL MS&T Specialist II Master’s degree Exp: 1 year |
This position is responsible for performing activities related to critical aspects of products and processes, including process development, pre-validation and optimization of solid oral dosage forms after Abbreviated New Drug Application (ANDA) filing throughout product launch and commercial lifecycle including validation. Executes studies with Research and Development (R & D), Laboratory Technical Services (LTS), manufacturing and planning. Maintains of expertise related to formulation, raw material properties and manufacturing processes. Identifies, analyzes and suggests corrective actions to optimize procedures, processes, materials, technology and regulatory compliance issues. Provides direction and training to other staff, technicians and manufacturing operators. | 09/11/2024 |
| 2559 | TG Therapeutics Remote, NY Research and Development Associate BS/BA or MS/MA/PhD degree in a scientific discipline Exp: 1 year |
We are seeking a dynamic and proactive Research and Development Associate to join our Regulatory Affairs team. This role will be instrumental in supporting the various aspects of product development including nonclinical and clinical research. The ideal candidate will have a strong life sciences background, with a passion to build a career in the pharmaceutical industry. We are looking for a highly motivated individual, who can be a team player and an independent thinker. This role will report to the Associate Director, Regulatory and Development Strategy. We are looking to fill this role in the Summer of 2024. | 09/11/2024 |
| 2560 | Thermofisher Greenville, NC QC Scientist II (Lab Services) Master's of Science in Chemistry, Biochemistry, Biology, or related physical science. Exp: 1-2 years |
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or growing productivity in their laboratories, we are here to support them. You will make an impact to our society by ensuring drug products manufacture onsite are safe and have excellent quality by performing various tests in a GMP laboratory. | 09/11/2024 |
| 2561 | Thermofisher WardHill, MA Engineer III, QA Master’s degree or foreign degree equivalent in Mechanical Engineering, Industrial Engineering, or a related field of study Exp: 0 years |
Support SQM team and core SQM processes with onboarding of new suppliers and materials; Assign, track and reconcile GMP documentation; Support Quality activities for key processes including Vendor/Supplier Change Notifications (VCN/SCNs) and Supplier Corrective Action Requests (SCARs); Establish and implement Quality Technical Agreements with suppliers; Construct internal and external audits as well as regulatory inspections; Support supplier status changes as required to ensure that the Approved Supplier (Vendor) List is accurate and complete; and Maintain filing system for the supplier quality documentation. | 09/11/2024 |
| 2562 | Thermofisher Remote/Knoxville, TN Engineer II, Field Service - SEM/TEM/FIB University degree in electronics, physics, engineering, computer science or similar field preferred Exp: 1-5 years |
The Field Service Engineer II for the Materials and Structural Analysis Division (MSD) of Thermo Fisher Scientific is responsible for performing the on-site installation, servicing and repair of complex equipment and systems. Engineers investigate and improve operational quality of system equipment; Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), Small/Large Dual Beam (SDB/LDB); instruct customers in the operation and maintenance of the system; serve as company liaison with customer on administrative and technical matters for assigned projects; and conduct on-site installations of the full range of Thermo Fisher Scientific electron microscopy systems and their associated options. | 09/11/2024 |
| 2563 | Thermofisher Greenville, NC Formulation Technician II Bachelor’s Exp: No exp |
The Formulation Technician II will be responsible to produce sterile injectables and work on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. This colleague follows written and verbal instructions when performing the following duties. | 09/11/2024 |
| 2564 | Thermofisher Remote/Boston, MA Engineer I, Field Service Bachelor’s degree in engineering, biology, chemistry, or related field. Exp: 1-3 years |
The Field Service Engineer (FSE) performs customer installs, repairs and preventative maintenance on a variety of laboratory instruments in assigned territory. The FSE engages with customers and provides the highest quality of service in a professional and timely manner. | 09/11/2024 |
| 2565 | Thermofisher Grand Island,, NY Scientist I, Process Development, Cell Biology Bachelor's degree in Biology, Bioengineering, Biochemistry, Chemical Engineering or equivalent required. Exp: 3 months |
Discover impactful work in the scientist I role on our process development team. You will be exposed to an outstanding variety of cell types and bioreactor operating experiences. Working with a team, you will modify and implement study plans, assemble data, and assess workflows with a focus on teamwork and continuous process improvement. | 09/11/2024 |
| 2566 | Thermofisher Logan, UT Engineer II, Mechanical Master's degree in Engineering (mechanical or chemical) Exp: 1 year |
Thermo Fisher Scientific is seeking a motivated Sustaining Engineer to join our R&D engineering team in Logan, UT. As part our Bioproduction Group, you will have the opportunity to support the developers and manufacturers of biological-based therapeutics and vaccines. Drive process and product innovation by adapting both existing and novel single-use technologies. Support new and existing product development pipeline through collaboration with the R&D teams to generate new product ideas, evaluate existing product and evaluate new technologies for feasibility and application into bioprocess workflows. Drive activities, including hands-on and delegated testing, writing test plans and results, presentations, interpretation of data and collaborate multi functionally to meet the business needs. | 09/11/2024 |
| 2567 | Pfizer Andover, MA Associate Scientist BA or BS in biology, microbiology, or related field Exp: 0-2 years |
The qualified candidate will join the Analytical R&D Microbiology organization to enable development of biological therapeutics in Andover, MA. The qualified candidate will be responsible for applying GMP microbiological methods (bioburden, LAL, PCR, etc.) in the assessment of product quality and detection of impurities to support GMP in-process, release, and stability testing of clinical supplies. This group also performs micro method qualifications and Environmental Monitoring (EM) of Drug Substance and Drug Product facilities. The individual is responsible for becoming proficient in aseptic lab technique and facility gowning for EM in various GMP facilities (Cell Banking, Drug Substance, Drug Product) as well as facility water collection & testing, facility gas system collection & testing. Other assays may include bioburden, endotoxin, microbial identifications, media qualification, qPCR (e.g. MMV), and sterility testing. The colleague must work within corporate guidelines and must appropriately record, archive and report all data as this is a cGMP compliant laboratory. The colleague must be able to interact effectively with peers and leaders as part of a multi-disciplinary team. The candidate must thrive in a fast-paced environment. Attention to detail, strong organizational skills, the ability to multitask and effective interpersonal, influencing skills and communication skills are required. | 09/05/2024 |
| 2568 | Pfizer McPherson, KS Lab Analyst I Bachelors degree in Chemistry, Microbiology, Biochemistry, or related scientific field Exp: 0+ years |
The Laboratory Analyst I participate is enrolled in a defined training curricula to gain competency performing routine chemical, biological and or microbiological assays of engineering and/or commercial product raw materials, production bulk samples, finished product, environmental monitoring samples, process & cleaning validation samples, package samples and components. | 09/05/2024 |
| 2569 | Pfizer Kalamazoo, MI QC Laboratory Analyst II (Third Shift) Bachelor’s degree in Chemistry, Biochemistry or related science Exp: 0-1 years |
This position is for a testing analyst in the Kalamazoo Laboratory working on third shift. Opportunity for schedule flexibility exists as the Laboratory supports business and customer needs on weekends and holidays. Technologies employed in the Rapid Turn Laboratory include HPLC, GC, titrations, Karl Fisher, UV, and general analytical procedures. You will be developing and applying your knowledge of procedures, techniques, tools, materials and equipment. Your receptiveness to new ideas will enhance the team’s ability to achieve goals and targets. You will follow standard procedures to complete tasks and identify process issues or problems that involve direct application of your skills/knowledge. | 09/05/2024 |
| 2570 | Pfizer Andover, MA Manufacturing Process Engineer III Master's in Engineering Exp: 1+ years |
Working with Pfizer’s dynamic engineering team, you will play a critical role in developing and modifying process equipment, automation and controls to meet desired quality standards. Your production engineering skills will help in recommending and implementing improvements, modifications or additions that will help in solving problems. As an Engineer III, your focus on this job will contribute to achieving project tasks and goals. It is your domain knowledge, commitment, collaboration and dedication that will help us achieve new milestones and patients across the globe. | 09/05/2024 |
| 2571 | BioIVT Durham, NC Science Associate I Bachelor’s degree (B.S./B.A.) Exp: 1 years |
Under general guidance the Associate Scientist I will work as part of a team to conduct cell culture in support of research and product production goals and our customers need for high quality primary human cells and services. | 09/05/2024 |
| 2572 | LGC Clinical Diagnostics Gaithersburg, MD Quality Control Analyst I Bachelor's degree in a scientific discipline or equivalent Exp: 1-3 years |
The Quality Control Analyst I will support manufacturing activities, perform routine laboratory maintenance, and conduct routine sample preparations and analyses. Work environments will include typing/computer work at a desktop workstation, sitting and/or standing at laboratory bench, and working in biosafety cabinets and chemical exhaust hoods. | 09/05/2024 |
| 2573 | SGS Saint Rose, LA Laboratory Analyst I Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 0-2 years |
Prepare and analyze samples with accuracy and precision in accordance to SGS' analytical SOPs. Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. Understand and apply basic analytical chemistry principles. Always follow safe laboratory practices and maintain a safe working environment. | 09/05/2024 |
| 2574 | SGS Orlando, FL Laboratory Analyst I, Volatiles Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 0-2 years |
Prepare and analyze samples with accuracy and precision in accordance to SGS' analytical SOPs. Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. Understand and apply basic analytical chemistry principles. Always follow safe laboratory practices and maintain a safe working environment. | 09/05/2024 |
| 2575 | SGS Reno, NV Lab Analyst I Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 1-2 years |
Our Reno, NV laboratory is looking for an entry-level Laboratory Analyst to join their team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory Analyst always follows safe laboratory practices and maintains a safe working environment. | 09/05/2024 |
| 2576 | SGS Las Vegas, NV Laboratory Analyst I Bachelor’s Degree in a Geology/Biology or similar scientific discipline Exp: 1-2 years |
Our Las Vegas, NV laboratory is looking for an entry-level Laboratory Analyst I to join their team! The Laboratory Analyst I prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst I works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst I understands and applies basic microscopic principles. The Laboratory Analyst I always follows safe laboratory practices and maintains a safe working environment. | 09/05/2024 |
| 2577 | SGS Saint Rose, LA Chemist Bachelor’s Degree in Chemistry or a related science preferred Exp: 1 year |
Responsible for analysis and reporting of various products such as crude oil, fuel oils, middle distillates, petroleum and petrochemicals, LPG & LNG gases, etc. | 09/05/2024 |
| 2578 | SGS Anchorage, AK Laboratory Analyst Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 1-2 years |
Our Anchorage, AK laboratory is looking for a Laboratory Analyst to join our team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory Analyst always follows safe laboratory practices and maintains a safe working environment. | 09/05/2024 |
| 2579 | SGS Deer Park, TX Chemist Bachelor’s Degree in Chemistry or a related science preferred Exp: 1 year |
Responsible for analysis and reporting of various products such as crude oil, fuel oils, middle distillates, petroleum and petrochemicals, LPG & LNG gases, etc. | 09/05/2024 |
| 2580 | Revvity San Diego, CA Biochemist II - Bacterial Cell Culture Bachelor of Science in Life Science or related area Exp: 6+ months |
This position is responsible for manufacturing cutting-edge recombinant protein research products in Molecular Cellular Immunology (MCI) group. The recombinant manufacturing associate will be involved in different stages of production of various recombinant protein products, which include recombinant protein expression and purification. The duties include preparing buffer solutions and cell culture media, performing bacterial cultures, affinity purifying recombinant proteins, and performing DNA isolation according to standard operating procedures. He or She may have additional responsibilities including transferring the products to other groups for testing, preparing product/project-related documentation, and maintaining the inventory and record for recombinant protein products. | 09/05/2024 |
| 2581 | Revvity San Diego, CA Research Associate I - Antibody Applications (IHC, ICC, Flow Cytometry, WB) Bachelor’s or Master's Degree in Biology, Immunology, Biochemistry, Neuroscience or other related fields Exp: 1 year |
Biolegend’s Research Associate position conducts antibody characterization and supports product development in Immunology, Oncology, Stem Cells and Neuroscience, encompassing various antibody applications including SDS-Page and Western blot, Immunoprecipitation, ELISA, flow cytometry, immunocytochemistry, immunohistochemistry, etc. This position will be responsible for effectively collecting, communicating and summarizing experimental data. | 09/05/2024 |
| 2582 | Revvity San Diego, CA Research Associate I - Tissue Culture Bachelor of Science in biology or a related field Exp: 1+ years |
This position is responsible for developing cutting-edge recombinant protein/antibody products in the Molecular & Cellular Biology (MCBio) group. The research associate will be involved in developing new lines of recombinant protein/antibody products by supporting projects and team members. The duties include preparing buffer solutions and cell culture media, maintaining cells cultures, and purifying recombinant proteins/antibodies according to standard operating procedures. Other job responsibilities include transferring the products to other groups for testing, preparing product/project-related documentation, and maintaining the inventory and record for recombinant protein/antibody products. This role will also support R&D projects to increase efficiencies or develop new technologies for the group. | 09/05/2024 |
| 2583 | Revvity Lafayette, CO Scientist I Bachelor's degree in chemistry or a life sciences discipline Exp: 1-3 years |
Revvity has a rewarding and exciting opportunity for an enthusiastic Scientist 1 for our Custom Synthetic Manufacturing laboratory. The Scientist 1 position will perform primary tasks in an ISO 9001:2015 laboratory in Lafayette, CO, Key responsibilities for this position include a wide array of duties related to the manufacturing of RNA and DNA oligonucleotides. This includes custom synthesis, cleaving, quality and quantity determination of product for customers. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry in multiple laboratories. | 09/05/2024 |
| 2584 | Societal CDMO Gainesville, GA QC Analyst I Bachelor’s Degree in chemistry or related scientific discipline Exp: 1 year |
We are looking for a QC Chemist I. In this role, you perform QC analytical activities in a highly regulated GMP environment. Activities include but are not limited to analytical method development, method validation, raw material testing, in process, release, and stability testing. Draft protocols, reports and procedures for analytical test methods, validation, and stability study. Hands on experience but not limited to HPLC, GC-FID, LC-MS, dissolution, FTIR, UV spectrophotometry, TOC, analytical balance, and Karl Fisher equipment. | 09/05/2024 |
| 2585 | Isolere Bio Research Triangle Park, NC Engineer/Scientist I - Reagent Development Bachelor’s Degree in engineering or other relevant scientific discipline Exp: 1-3 years |
As an Engineer/ Scientist I in the Reagent Development team, you will support the development and scaling of IsoTag™ reagents by producing smaller scale lots for testing and further development. The Development team is responsible for scaling production processes from the R&D team and optimizing them for use in manufacturing. This role will also assist with the initial production of IsoTag™ reagents with the manufacturing team, assisting with qualifying and validating the reagent production processes. | 09/05/2024 |
| 2586 | Hologic San Diego, CA Research Associate 2 B.A. /B.S. Molecular Biology, Chemistry, Biochemistry or related field Exp: 1-3 years |
Hologic is seeking a Research Associate 2 responsible for designing and performing experiments to support assay development including: feasibility, design transfer, assay integration and assay verification. Candidate accountable for effectively communicating results, collaborating with team members, and troubleshooting. | 09/05/2024 |
| 2587 | Hologic Newark, DE Senior EMC/RF Compliance Engineer Master’s Degree Exp: 1-3 years |
The Senior Compliance Engineer will be responsible for defining and executing product compliance strategies, policies, and processes to ensure that the company’s products meet regulatory standards and compliance certifications are obtained and maintained for global markets (e.g., ISO, FCC, UL, IEEE). The Senior Compliance Engineer will work closely with regulatory agencies and is the technical subject matter expert for regulatory compliance. Apply today! | 09/05/2024 |
| 2588 | Hologic Newark, DE Senior Electrical Engineer Masters Degree Exp: 1-3 years |
Hologic is seeking Senior Electrical Engineer to lead the design of a complete and complex framework, system, and products. You will be expected to design, develop, modify and evaluate components and processes used in the generation, manipulation, transmission and storage of electricity. You will be expected to determine design approaches and parameters. | 09/05/2024 |
| 2589 | Hologic San Diego, CA Mechanical Design Engineer 1 BS in Mechanical Engineering Exp: 0-3 years |
In this role, you will be part of a multidisciplinary engineering team developing and sustaining medical diagnostic instruments including mechanical design and manufacturing. You will be expected to bring hands-on experience and knowledge in mechanical design and manufacturing while utilizing sound engineering judgement and first principals. You will be expected to design, prototype, and test various electromechanical concepts to provide rapid feedback and direction to the broader development team to drive fast and decisive decisions. Interfacing with outside vendors on rapid prototyping, machining, molding, and advanced manufacturing processes is required. This is a fast-paced position that demands the ability to quickly adapt to evolving changes within the instrument, assay, and user needs. You will be working across functional groups such as Systems Engineering, Assay Development, Manufacturing, and Process Transfer. Clear communication, the ability to collaborate with others, and being a self-starter are a must. | 09/05/2024 |
| 2590 | SonoThera South SF, CA Temporary Research Associate, Protein/Metabolome Analytics Bachelor's degree in the biological sciences Exp: 0-3 years |
The Gene Therapy group at SonoThera is seeking to hire an entry-level Research Associate to become an integral part of the gene therapy drug development effort. We seek candidates who think critically and have the desire and ability to learn new techniques. This position requires adaptability and an ability to perform at a high level in a fast-paced environment. A qualified candidate will have technical experience in preparation of samples for protein and metabolite analyses. In this position, you will play an integral role in characterizing gene therapy vector delivery efficiency in diverse preclinical models. You will develop and optimize protocols for multiple assays, including but not limited to, immunoassays (ex. ELISA/MSD, Western blot, etc.), colorimetric and enzymatic assays for various efficacy and safety endpoints. | 09/05/2024 |
| 2591 | SouthernBiotech Birmingham, AL Quality Control Technician Bachelor’s Degree in Science Exp: 1 year |
We are currently seeking a Quality Control Technician for testing products, such as antibodies and proteins, following SOP’s and ISO requirements. | 09/05/2024 |
| 2592 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist II BA/BS Chemistry Exp: 1 year |
The primary function of a QC Chemist II is to perform to a high level in qualitative and quantitative chemical and physical analysis in support of two of the following areas: Analysis of raw materials and packaging components, Analysis of in-process and finished drug products (including stability) of primarily high-volume products, Analysis of high potency products | 09/05/2024 |
| 2593 | Spanios Houston, TX Project Bioengineer I MS in Bioengineering Exp: 1 year |
This job is suitable for an individual with meticulous skills for compilation, analysis, presentations, and communication of data from multiple projects with the CSO and COO for the purpose of documentation and communication with the clients. Someone who can co-ordinate Research Associates working on different projects to receive data for further distribution. This position will offer a unique and rewarding translational research experience in a dynamic and highly productive environment. | 09/05/2024 |
| 2594 | Spanios Houston, TX Research Associate I Bachelors degree Exp: 1 year |
This job is suitable for a responsible, skilled individual someone who can handle multiple projects and can follow instructions to complete assignments under minimal supervision. This position will offer a unique and rewarding translational research experience in a dynamic and highly productive environment. As a Research Associate you will provide responsible assistance for establishment and propagation of organoid cultures. | 09/05/2024 |
| 2595 | Spark Therapeutics Philadelphia, PA PD Downstream Scientist MS in chemical engineering, biochemistry, chemistry, biophysics, or related area Exp: 0-4 years |
The downstream process development (DSPD) team is seeking a highly motivated and innovative scientist to join our downstream purification technology development team. The successful candidate should have solid technical training in scientific and/or engineering discipline, preferably having biopharmaceutical industry experience. She/he will participate in multiple downstream process development projects for early or late phase program, with a focus on developing platform technology, continued process and product understanding and bringing innovation in adeno-associated virus (AAV) vector purification and characterization. | 09/05/2024 |
| 2596 | Spark Therapeutics Philadelphia, PA Research Associate - Upstream Process Development B.S. in chemical engineering, chemistry, biochemistry, or biology/molecular biology or related area Exp: 0-2 years |
The Upstream Process Development Research Associate is involved in the execution of recombinant adeno-associated viral vector (rAAV) production processes. The Research Associate executes experiments, aggregates and reviews experimental data, verifies data in technical reports and works under supervision of senior technical leads. | 09/05/2024 |
| 2597 | SparX Mount Prospect, IL Research Associate, in vitro Pharmacology Master’s degree in cell biology, oncology, immunology or related field Exp: 1 year |
SparX is looking for a highly motivated, interactive and creative Research Scientist with a strong cell biology background to join the pharmacology team. The primary responsibilities of the Research Associate will be to develop and perform in vitro cellular and/or biochemical assays for antibody drug candidates screening, biological function evaluation in immuno-oncology and oncology drug discovery program. | 09/05/2024 |
| 2598 | WuXi Advanced Therapies Philadelphia, PA Quality Control Environmental Monitoring Associate I Bachelor’s degree with a major in Biology, Microbiology, or related Life Science Exp: 0-3 years |
The Quality Control Environmental Monitoring Associate I is responsible for performing sampling and testing in support of manufacturing and validation activities, under the direction of a Supervisor or higher. Works in a team environment with various laboratory staff. | 09/05/2024 |
| 2599 | HD Biosciences San Diego, CA Research Associate I Bachelors in Life Sciences or related field preferred Exp: 0-1 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its Discovery Biomarkers team. We’re seeking a highly motivated Research Associate I to support our in vitro/ex vivo immunology team for various projects. | 09/05/2024 |
| 2600 | WuXi Advanced Therapies Philadelphia, PA Manufacturing Associate I - 1st Shift Bachelor’s (science preferred) degree Exp: 0-2 years |
The Manufacturing Associate I is responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 09/05/2024 |
| 2601 | HD Biosciences San Diego, CA Research Associate II (Temp/Contingent) Master degree in Molecular and Cell Biology or Bachelor degree Exp: 1-2 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 09/05/2024 |
| 2602 | Staar Surgical Monrovia, CA Quality Engineer I Bachelor’s degree, preferably in science or engineering Exp: 1 year |
Support site production, operations, and quality and R&D teams by addressing emergent issues that might arise due to the operation processes. Serve as the quality representative during any product or process investigation. Lead investigations including root cause analysis and health risk assessment of the identified product or process nonconformities. Prepare and execute validations, technical studies, test method validations and other studies / reports as required. This includes preparation of protocols, establishment of test methodology and acceptance criteria, training personnel, execution, data analysis, investigation, and writing final reports. Support project teams on non-conformance investigations regarding component failures, finished goods failures, and product returns. This includes but is not limited to performing risk analysis, determining root cause and recommending corrective action and SCRs. | 09/05/2024 |
| 2603 | Stability Biologics San Antonio, TX QA Specialist BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.) Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 09/05/2024 |
| 2604 | Stellartech Research Corporation Milpitas, CA Associate Quality Engineer Bachelor’s degree or equivalent Exp: Entry level |
Perform quality engineering development activities for new product designs by assisting Engineering in the preparation of design and development plans, Design History File documentation, and Design History File preparation. Review and approve Device Master Record documentation for new product design and maintenance, including bills of material, assembly procedures, manufacturing operations, assembly diagrams, test procedures, component specifications, labeling, and operator’s manuals. Perform ongoing quality engineering activities on current products to improve product designs and/or manufacturing processes including participation in NCM, Complaint, and CAPA investigations and actions as necessary. Assist in process validation activities for new and current products. Assist in maintenance and improvement of the Quality System with guidance of QA Management, including internal audits, external audits, and quality improvement activities. Assist Engineering in the preparation and execution of verification and validation protocols and verification and validation test reports for new products and changes to current products. | 09/05/2024 |
| 2605 | Stereotaxis St. Louis, MO System Test Engineer Bachelor's degree in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, or other related degree highly preferred Exp: 1-2 years |
The System Test Engineer will be working within the system test team and collaborating with a cross-functional team to test and commercialize Stereotaxis products. The role will be working alongside various engineering disciplines and participating in development of test cases used for design verification and design validation activities in an ever-changing environment. | 09/05/2024 |
| 2606 | STERIS Coon Rapids, MN Scientist I - Validations B.S. degree in a technical discipline (engineering, physics, biology, chemistry, etc.) Exp: Entry level |
Responsible for the activities related to the coordination of validation of sterilization processes across STERIS operating facilities. This will NOT be a laboratory-based position. Activities include calibration of data collection systems, such as maintaining dosimeters and dosimetry equipment, measurement of dosimeters for report generation; operation, and data collection related to portable temperature/humidity sensors; coordinating with external laboratories for equipment calibrations and maintenance; coordinating with Customers for test sample processing and requalification studies; coordination and proper handling of product samples for transfer to outside laboratories for testing; and other routine tasks as directed by the immediate supervisor or manager. | 09/05/2024 |
| 2607 | Radionetics Oncology San Diego, CA Research Associate I Bachelor’s degree in biology or a related scientific discipline. Exp: 1 year |
The Research Associate I (RA) is a highly motivated lab bench scientist that contributes to multiple active research programs and is a valuable member of a collaborative team. The RA maintains cell lines, validates antibodies for flow cytometry, and performs flow cytometry analysis to determine target protein copy number at the cell surface to support cell line selection for in vivo model development for lead compound identification. The RA analyzes and interprets flow cytometry data and presents results in in vitro team meetings. The RA adopts and learns new processes quickly to be able to operate independently at the bench. | 08/30/2024 |
| 2608 | RayzeBio Indianapolis, IN Production Operator, Isotope Production Bachelor’s Degree in a STEM field Exp: 1-4 years |
The Operator – Isotope Production will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As Operator – Isotope Production, you will be instrumental in implementing a novel isotope production program that will manufacture the clinical and commercial scale radioisotopes for RayzeBio’s drug products. This individual will be part of a team responsible for producing RayzeBio’s radioisotopes under Good Manufacturing Practices (GMP). Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. The Operator – Isotope Production will report directly to the operations leader of Isotope Production. Operator level will be evaluated with experience and qualifications. | 08/30/2024 |
| 2609 | RayzeBio Indianapolis, IN Radiopharmaceuticals Production Operator II Bachelor’s Degree in a STEM field Exp: 1-4 years |
The Radiopharmaceuticals Production Operator will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As the Production Operator, you will play an active role in daily operations, striving to ensure each batch is right the first time and that the production area is kept in order at our manufacturing site in Indianapolis IN. You will be responsible for the production of RayzeBio drug products, strictly complying with good manufacturing practice and aseptic requirements. Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. As RayzeBio expands the production site and its portfolio of new products, the Production Operator will support validation work for future company initiatives, and support management with internal projects and new hire training. The Radiopharmaceuticals Production Operator will report directly to the Production Manager. Operator level will be evaluated with experience and qualifications. | 08/30/2024 |
| 2610 | RayzeBio San Diego, CA Associate Scientist I/II, Chemistry BS or MS in Chemistry or related field with strong understanding of organic and analytical chemistry Exp: BS 2-5 years’ or MS 0-4 years’ |
The Associate Scientist will work as part of a team of scientists to synthesize and design analogs to optimize potency, pharmacokinetics, and in vivo efficacy of potential drug candidates. | 08/30/2024 |
| 2611 | Reckitt Wanamingo, MN Compliance Assurance Lead Bachelor’s Degree in technical discipline (science/ engineering/ food processing, etc) Exp: 0-2+ years |
Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers. | 08/30/2024 |
| 2612 | Reckitt St. Louis, MO Project Engineer B.S. Engineering Discipline (Electrical, Chemical, Mechanical) Exp: 1-3 years |
Seeking an engineering leader eager to make an impact! As the Engineering Manager within one of our agile-factory teams, you'll be the spark that drives project efficiency and innovation. Be at the forefront of managing an exceptional team, turning strategic plans into reality and leading the charge in our manufacturing success. Standard engineering is not what we do – we're about pioneering. If you're passionate about leading change and enhancing how we operate, you could be the perfect fit for us. | 08/30/2024 |
| 2613 | Reckitt St. Peters, MO Project Engineer B.S. Engineering Discipline (Electrical, Chemical, Mechanical) Exp: 1-3 years |
Seeking an engineering leader eager to make an impact! As the Engineering Manager within one of our agile-factory teams, you'll be the spark that drives project efficiency and innovation. Be at the forefront of managing an exceptional team, turning strategic plans into reality and leading the charge in our manufacturing success. Standard engineering is not what we do – we're about pioneering. If you're passionate about leading change and enhancing how we operate, you could be the perfect fit for us. | 08/30/2024 |
| 2614 | RefleXion Medical Hayward, CA Installation Engineer - Hybrid Bachelor’s of Science (BS) degree in electrical, mechanical or similar engineering field Exp: Recent College Grads encouraged to apply! |
The Installation Engineer will perform installations of RefleXion’s breakthrough radiation therapy technology at customer sites. The Installation Engineer must be proficient with hands-on equipment assembly and testing. The Installation Engineer will interact with various customer stakeholders and RefleXion resources with the highest level of professionalism and competence. | 08/30/2024 |
| 2615 | Regel Therapeutics Cambridge, MA Research Associate, Molecular Biology BA/BS or MS in biology or related field Exp: 1-3 years |
Regel Therapeutics is a gene modulation therapy company focused on improving the life of patients suffering from disorders resulting from alteration of gene expression. Our proven T3 (Targeted Therapeutic Technology) platform combines AAV delivery with two proprietary technologies for efficient and specific restoration of gene expression exclusively in the cells affected by the pathology. We are a seed-stage startup based in Cambridge, MA and Berkeley, CA and we are looking for a talented Research Associate to join our R&D team to help develop our preclinical programs. Perform molecular analysis of nucleic acid and protein levels in animal tissue to support preclinical development efforts. Maintain organized and detailed documentation of activities in an electronic notebook. Communicate research findings to the R&D team | 08/30/2024 |
| 2616 | Regeneron East Greenbush, NY Associate Process Characterization & Technology Scientist B.S in Biology, Chemistry, Biochemistry or related life sciences field. Exp: 0-2 years |
Regeneron is currently looking for a Process Characterization & Technology Scientist to join the process characterization and controls cell culture team within the Process Sciences department. This is a lab based position with a 1st shift, Wednesday- Saturday, 6am-4:30pm schedule. The Process Characterization and Technology Scientist is responsible for characterizing the cell culture manufacturing operations through laboratory-scale experiments, drawing conclusions via statistical analysis, and authoring technical summary reports. | 08/30/2024 |
| 2617 | Regeneron Tarrytown, NY Laboratory Assistant II, Analytical Chemistry BS Exp: 0-2+ years |
The Laboratory Assistant II will support the staff members in the Analytical Chemistry group through general administrative duties as well as laboratory and equipment upkeep. | 08/30/2024 |
| 2618 | Regeneron Tarrytown, NY Associate Scientist - DNA Core BS/MS Exp: 0-3 years |
We are seeking a collaborative and motivated Associate Scientist to join the DNA Core. Our group provides Regeneron laboratories with services vital for conducting scientific research, including plasmid preparation and purification. | 08/30/2024 |
| 2619 | Regeneron East Greenbush, NY Associate Process Characterization & Technology Scientist B.S in Biology, Chemistry, Biochemistry or related life sciences field. Exp: 0-2 years |
Regeneron is currently looking for a Process Characterization & Technology Scientist to join the process characterization and controls cell culture team within the Process Sciences department. This is a lab based position with a 1st shift, Wednesday- Saturday, 6am-4:30pm schedule. The Process Characterization and Technology Scientist is responsible for characterizing the cell culture manufacturing operations through laboratory-scale experiments, drawing conclusions via statistical analysis, and authoring technical summary reports. | 08/30/2024 |
| 2620 | Regeneron Rensselaer, NY QC Analyst - Sample Management BS/BA in Life Sciences, or related field Exp: 12-18+ months |
Regeneron is currently looking to fill a QC Analyst position in our QC Sample Management department with a 3rd shift schedule, Saturday-Wednesday, 10pm-8:30am. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Quality Control’s role is to ensure product quality and patient safety. Our QC Sample Management department acts as the gatekeepers of QC, accessioning and triaging samples as they are submitted for testing; the QC Analyst position performs a variety of sample receipt functions as well as routine sample inventory and disposal. | 08/30/2024 |
| 2621 | Regeneron Tarrytown, NY Associate Scientist BS degree or MS degree in a scientific field Exp: 0-3+ years |
Regeneron's Clinical Bioanalysis group, located in Tarrytown NY, is seeking an Associate Scientist. Train on bioanalytical methods (manual, hybrid, and automated) and completes methods to perform bioanalysis for clinical studies under supervision. Analyze multiple plates within the same day and may perform multiple assays within the same day. Interpret data to assess plate acceptance criteria and adjust sample dilutions accordingly. Complete vital operations in LIMS (requesting samples, building analysis plates, tracking sample movement, tracking pending analysis and performing data entry). Uses the ELN for data documentation purposes. Prepares and qualifies reagents, and re-orders laboratory supplies and reagents, as needed. Ensures compliance, as appropriate, for all laboratory work and documentation in accordance with working practices, company SOPs, bioanalytical method procedures (BMPs), and regulations. | 08/30/2024 |
| 2622 | Regeneron Rensselaer, NY Associate Biotech Production Specialists BS/BA in Life Sciences or related field Exp: Entry Level, New Grad |
Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Associate Biotech Production Specialists are on the front line, producing our life changing products and have a passion for assisting those in need by using biotechnology. They perform all tasks necessary for the manufacturing operations of both clinical and commercial manufacturing programs. | 08/30/2024 |
| 2623 | Renaissance Lakewood, NJ Compounder II, 3rd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 08/30/2024 |
| 2624 | Renaissance Lakewood, NJ Compounder II, 3rd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 08/30/2024 |
| 2625 | Renaissance Lakewood, NJ Compounder II, 2nd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 08/30/2024 |
| 2626 | Renaissance Lakewood, NJ Compounder II, 2nd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 08/30/2024 |
| 2627 | Rigel Pharmaceuticals South SF, CA Clinical Trial Assistant Bachelor’s degree in science related field required. Exp: 1-2 years |
This opportunity will support the Clinical Operations team in a fast paced, busy hematology/oncology pharmaceutical development department. As a Clinical Trial Assistant (CTA), you will assist the clinical research teams in clinical trial conduct, oversight, and logistics by providing administration and project tracking support. | 08/30/2024 |
| 2628 | RION Rochester, MN Research Associate Bachelor’s or Master’s degree with focus in Biological Sciences Exp: 1+ years |
The Research Associate will contribute to ongoing scientific projects within the Research and Development laboratory focused on Rion’s exosome technology. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, flow cytometry, ELISA, RT-qPCR, and colorimetric/fluorometric-based assays. The Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Research Associate will work closely with the Research and Development Scientists and support the efforts of Quality Control and Process Development. As such, the successful candidate will work in an upbeat, highly collaborative and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 08/30/2024 |
| 2629 | Sai Life Sciences Watertown, MA Senior Research Associate - Biology Master's degree in Biology Exp: 1+ years |
As the Senior Research Associate in Biology, you will play a crucial role in conducting groundbreaking research, contributing to our mission of advancing scientific knowledge and addressing pressing biological challenges. Working closely with our team of scientists, you will be involved in various aspects of experimental design, data collection, analysis, and interpretation. This position offers an exciting opportunity to be at the forefront of scientific discovery and make a meaningful impact in the field of biology. You’ll have the opportunity to develop your skills to work independently and advance your knowledge-base on assay development and optimization. | 08/30/2024 |
| 2630 | Sai Life Sciences Watertown, MA Research Associate - Biology Bachelor's or Master's degree in Biology Exp: 1+ years |
As the Research Associate in Biology, you will play a crucial role in conducting groundbreaking research, contributing to our mission of advancing scientific knowledge and addressing pressing biological challenges. Working closely with our team of scientists, you will be involved in various aspects of experimental design, data collection, analysis, and interpretation. This position offers an exciting opportunity to be at the forefront of scientific discovery and make a meaningful impact in the field of biology. | 08/30/2024 |
| 2631 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelors Exp: 0+ years |
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as a Production Technician - Vaccine within our Packaging Team, will have the potential to transform the practice of medicine, turning the impossible into possible for millions of people. | 08/30/2024 |
| 2632 | Sanofi Chattanooga, TN Quality Control Chemist Lab I (2nd shift) Bachelor’s degree in chemistry or related field Exp: 0-3 years |
The Quality Control Lab Chemist will perform routine testing to support production and release of product in compliance with established specifications. Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented, and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures.Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. | 08/30/2024 |
| 2633 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelors Exp: 0+ years |
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as a Production Technician - Vaccine within our Packaging Team, will have the potential to transform the practice of medicine, turning the impossible into possible for millions of people. | 08/30/2024 |
| 2634 | Sanofi Chattanooga, TN Quality Control Lab Chemist I Bachelor’s degree in chemistry or related field Exp: 1-3 years |
The Quality Control Lab Chemist will perform routine testing to support production and release of product in compliance with established specifications. Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented, and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures.Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. | 08/30/2024 |
| 2635 | Sanofi Waltham, MA Senior Associate Scientist MSc or BSc Exp: MSc: +1 year; BSc: +1-3 years |
The primary responsibilities of the Senior Associate Scientist, Virology will be to support covid vaccine projects by generating and characterizing SARS-CoV-2 pseudovirus materials and maintaining the production lab. Individual will support optimization of pseudovirus capabilities and assay development as needed for the project and departments. The successful candidate will be required to generate, analyse and document data and to communicate their results internally. The candidate will be required to liaise effectively with the team. | 08/30/2024 |
| 2636 | Santa Cruz Biotechnology Paso Robles, CA Research Assistant Bachelor of Science in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: Entry Level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from supervisor. Strong scientific background and business communication skills. | 08/30/2024 |
| 2637 | Santa Cruz Biotechnology Santa Cruz, CA Research Assistant Bachelor of Science in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: Entry Level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from supervisor. Strong scientific background and business communication skills. | 08/30/2024 |
| 2638 | Sapere Bio Research Triangle Park, NC General Supervisor, CLIA Laboratory Master's or Bachelor’s degree in clinical laboratory science, medical technology or chemical, physical, or biological science Exp: 1 year |
The General Supervisor provides day-to-day supervision of testing personnel. The General Supervisor is responsible for the proper performance of all laboratory procedures and reporting of test results.Perform accurate and timely laboratory testing according to SOPs within the allowable timeframe. Demonstrate the ability to use good judgement and independent thinking in data analysis and interpretation of patient results. Maintain all Quality Management System on instrument maintenance programs, i.e. preventative maintenance, cleanliness, and maintains records of service in compliance with CLIA. Review testing issues with the Technical Supervisor to get direction for troubleshooting and next steps. Ensure that all remedial actions are taken whenever test systems deviate from the laboratory's established performance specification. Provide leadership and direct a team of technologists through positive communication and support. Train new personnel with regard to technical and operational procedures. Ensure all laboratory members are proficient in assay processing, including biannual (first year) and subsequent annual competency training. Work with the lab team to monitor and maintain inventory of supplies and place orders of materials. Participate in managing all governmental and regulatory audits. Manage and monitor Quality Control (QC), Quality Assurance (QA), Safety and Inspection practices to assure compliance with CLIA regulations. | 08/30/2024 |
| 2639 | Saptalis Hauppauge, NY Analytical Scientist B.S/M.S/Ph.D in Analytical Chemistry or related discipline Exp: 0-2 years |
Saptalis is looking to recruit Analytical Scientists to join the growing Analytical R&D group at our facility in Hauppauge, NY. Analytical Scientist is responsible for developing and validating analytical methods for analytes of interest in new drug products using UPLC, HPLC, GC and other analytical instruments. Execute all functions in accordance with current FDA regulations, ICH guide lines, USP methodologies, cGLPs and Saptalis SOPs. | 08/30/2024 |
| 2640 | Saptalis Hauppauge, NY Quality Control Scientist BS/MS Degree (chemistry or related field) Exp: 0-2 years |
Saptalis is looking to recruit QC Scientists to join the growing Quality group at our facility in Hauppauge, NY. QC Scientist is responsible for GMP testing of raw materials, in-process, finished product and stability samples for release. In addition, the responsibilities include maintaining laboratory equipment, assisting in investigations and coordinating external testing as needed. | 08/30/2024 |
| 2641 | Saptalis Hauppauge, NY Validation Associate Bachelor’s degree required, preferably in a science or engineering related field. Exp: 0-2 years |
Saptalis is looking to recruit a Validation Associate to join a growing Technical Operations group at our facility in Hauppauge, NY. Validation Associate is responsible for execution of qualification and validation programs for processing and testing equipment, computer systems, manufacturing processes and cleaning of manufacturing equipment as per FDA regulations and SOPs. | 08/30/2024 |
| 2642 | Scanogen Baltimore, MD Research Associate Bachelor in molecular biology, biotechnology, bioinformatics, biology, chemical engineering, bioengineering or related field Exp: 1 year |
To test and perform manual and automated molecular diagnostic assays. Perform and assist with bacterial and fungal cultures. Perform and assist with bacterial and fungal lysate preparation. Collect, prepare and process bacterial and fungal specimens. Collect and document research data. | 08/30/2024 |
| 2643 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements | 08/30/2024 |
| 2644 | Sciecure Pharma Monmouth Junction, NJ Project Coordinator Bachelor’s degree in Life Science (Biology, Chemistry, Chemical Engineering, Etc.). Exp: 1-3 years |
Sciecure Pharma Inc. specializes in the research and development of pharmaceutical finished products from conception to commercial. Our growing company is seeking to hire a project coordinator who will be in charge of assisting in organizing our ongoing projects. This task involves monitoring project plans, schedules, organizing and participating in stakeholder meetings, and ensuring that project deadlines are met in a timely manner. To be successful as a project coordinator, you will need to be able to work on tight deadlines, be competent in using Microsoft Office applications such as Word and Excel, and have exceptional verbal, written, and presentation skills. A bachelor’s degree in life science is required for consideration. | 08/30/2024 |
| 2645 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science Exp: 1 year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 08/30/2024 |
| 2646 | Scientific Protein Laboratories Waunakee, WI Validation Associate B.S. in Chemistry, Biological Sciences or Engineering (Chemical, Electrical, Mechanical, Reliability) or related discipline Exp: No Exp |
Join our team at Scientific Protein Laboratories (SPL), a world leader in biosourced pharmaceuticals, located just outside of Madison, Wisconsin in Waunakee! SPL is an innovative biopharmaceutical leader with unique products and services supporting the pharmaceutical industry globally. For over 40 years, SPL specializes in the development and cGMP compliant manufacturing of Active Pharmaceutical Ingredients (APIs). SPL has an exciting opportunity to join the team as a Validation Specialist. This position is responsible for preparing and executing validation protocols for cGMP processes, production/laboratory equipment, cleaning procedures, and software in compliance with Q7. Writes final reports for executed validation protocols. Assists other Validation staff with their validation protocols. | 08/30/2024 |
| 2647 | Pfizer Bothell, WA Senior Associate Scientist- Conjugation M.S. degree Exp: 0-2 years |
The Protein and Bioanalytical Sciences (PBS) team is focused on creating and delivering novel research test articles for preclinical evaluation. As a Senior Associate Scientist, you will be at the center of our operations, and you’ll find that everything we do is in line with an unwavering commitment to quality. This position is responsible for preparing and analyzing novel Antibody Drug Conjugations (ADCs), developing new conjugation methods and analytical assays, and delivering critical reagents. This person will play a critical role in supporting Pfizer Oncology’s preclinical programs. Your strong foundation in quality scientific practices will help the team in meeting critical deadlines and exceeding milestones. You will be relied on as a technical contributor to make decisions that involve direct application of your knowledge. It is your hard work and focus that will make Pfizer ready to achieve new breakthroughs and help patients across the globe. | 08/21/2024 |
| 2648 | Pfizer Groton, CT Manufacturing Engineer Bachelors Level qualification in Chemical Engineering, Pharmaceutical Sciences, Materials Science or other Engineering discipline. Exp: For a newly qualified graduate or graduate with some initial industrial experience |
We are seeking a highly motivated person as Manufacturing Engineer in our Drug Product Manufacturing (DPM) facility. The successful candidate will learn and actively support a wide range of process development and manufacturing activities for clinical drug product supplies. Additionally, the colleague will contribute to the development of DPM technology capabilities (eg. Powder blending, granulation, tablet compression, encapsulation, film coating etc.) by supporting novel process development and process understanding studies. The successful candidate must demonstrate strong teamwork dynamics when interfacing with various groups (e.g., Operations, Quality, Tech Support) and a continuous improvement mindset. | 08/21/2024 |
| 2649 | Pfizer Pearl River, NY Lab Process Control Associate Bachelor’s degree in a relevant field (eg, science, business administration) Exp: 0-2 years |
The Lab Process Control Associate (P01) will report directly to CIHO’s Laboratory Process Control Lead and play a major role in ensuring operational excellence in CIHO’s compliant testing laboratories. The primary responsibility for this position is to assist CIHO’s Lab Process Control Lead to achieve success in aligning laboratory compliance across CIHO, which includes improving the lab process control document cycle times. The position will help the Laboratory Process Control Lead manage several Lab Process Control workflows including but is not limited to (i) Standard Operating Procedures (SOP) undergoing periodic review (authoring, review and approval); (ii) Laboratory Deviation Reports (LDR), Planned Deviation Notes (PDN), and Change Control Requests (CCR) from initiation through approval, required deliverables and any post approval commitments. Other routine duties will include (i) verification of documents associated with laboratory equipment qualification reports; (ii) standardization of common verbiage used in these CIHO documents; (iii) providing assistance in conducting LDR investigations. | 08/21/2024 |
| 2650 | Pfizer Pearl River, NY Associate Scientist - Clinical Immunology & High-Throughput Operations Bachelor's Degree in a relevant scientific discipline Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support the technology transfer and integration of new laboratory immunoassays into the cGLP space, support assay validation projects and monitor immunoassay lifecycle. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 08/21/2024 |
| 2651 | Pfizer Pearl River, NY Associate Scientist, High-Throughput Clinical Immunoassays and Diagnostics Bachelor's Degree in a relevant scientific discipline Exp: 0-3 Years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. The primary purpose of this position is to assist, develop and perform all aspects of preclinical and clinical functional assays, including, but not limited to serum bactericidal assay (SBA) using robotics or manual method, including all required documentation. Also, included activities are preparation of buffers, media, qualification of assay reagents and other duties assigned as necessary. All of the above includes practicing laboratory safety at all times. All work is to be done in a compliant manner according to relevant SOP guidelines and GLP and/or GMP guidelines, as required. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 08/21/2024 |
| 2652 | Pfizer Sanford, NC Technical Operations Engineer Bachelor's degree in any of the following disciplines: Chemistry, Biochemistry, Biotechnology, Chemical Engineering, and/or Biology Exp: 0+ years |
Working with Pfizer’s dynamic engineering team, you will play a critical role in supporting efforts to bring products from research to manufacturing. You will leverage your technical capabilities to understand the inherent problems of transfer of technology from the research stage to manufacturing, in cooperation with pilot-plant and production departments. You will conduct assessments and create procedures for materials and components used throughout the stages of production.As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues. | 08/21/2024 |
| 2653 | Pfizer Pearl River, NY Associate Scientist - Sample Logistics and Solutions Bachelor of Science Degree Exp: 0-5 years |
The primary purpose of this job role is to function as a member of the Sample Logistics and Solutions (SLS) team within Pfizer Vaccine Research and Development (VRD). The incumbent will be responsible for receiving samples from global clinical/study trials according to approved protocols and processes. The individual will participate in all aspects of tracking and documenting the chain of custody of samples. The incumbent’s role will include sample receipt, documentation, storage, tracking, aliquoting, distribution to the testing labs, and sample disposal. The colleague will work in a team setting and will share roles and responsibilities as assigned by the team leader/manager. | 08/21/2024 |
| 2654 | Pharmaron Exton, PA Associate Scientist Bachelor of Science (Biology, Biochemistry, Pharmaceutical Life Sciences) Exp: 0-2 years |
Associate Scientist within our Cell Biology team is a pivotal role which requires a dynamic professional with strong experience in conducting various studies/assays while delivering exceptional quality with high attention-to-detail to ensure all clients expectations are met. | 08/21/2024 |
| 2655 | Pharpoint Research Durham, NC Quality Assurance Auditor Bachelor’s degree (B.A./B.S.) or equivalent in a scientific, computer, or related discipline. Exp: 1-2 years |
Performs project and non-project quality assurance duties at PharPoint Research. Responsible for carrying out quality initiatives at the company, including but not limited to SOPs and training, computer systems validation, and Quality Management System | 08/21/2024 |
| 2656 | Pierre Fabre Remote, Cell Therapy Operations Specialist, Associate I Bachelor's degree in science or health-related field required Exp: 1 year |
Pierre Fabre Pharmaceuticals is seeking a highly motivated, and well-organized Cell Therapy Operations Specialist (CTOS). This role will be the central point of contact for Health Care Professionals (HCP) from product availability inquiry through product receipt at the institutions. Additionally, this role will be responsible for selecting the product lot for the patient that meets the matching requirements, as well as answering and triage all inbound calls from HCPs. | 08/21/2024 |
| 2657 | Pierre Fabre Parsippany, NJ Cell Therapy Operations Specialist, Associate I Bachelor's degree in science or health-related field required Exp: 1 year |
Pierre Fabre Pharmaceuticals is seeking a highly motivated, and well-organized Cell Therapy Operations Specialist (CTOS). This role will be the central point of contact for Health Care Professionals (HCP) from product availability inquiry through product receipt at the institutions. Additionally, this role will be responsible for selecting the product lot for the patient that meets the matching requirements, as well as answering and triage all inbound calls from HCPs. | 08/21/2024 |
| 2658 | Poseida Therapeutics San Diego, CA TEMPORARY - Process Development Associate Bachelor’s or Master’s degree in Biological Sciences, Biomedical Engineering, Immunology or other related scientific field Exp: 0-2 years |
We are seeking an experienced and motivated Process Development Associate to join the late-stage Process Development & Manufacturing Sciences and Technology(MSAT) team at Poseida Therapeutics. The successful candidate will join a multidisciplinary team to support the allogeneic efforts for Poseida’s first allogeneic programs, as well as ongoing process changes for the clinical-stage autologous programs. This is a hands-on, laboratory-based role where the candidate will support the introduction and evaluation of new technologies into Poseida’s allogeneic processes and play a key role in process understanding. The ideal candidate will be a cell biologist/biological engineer with a proven track record of innovation, knowledge in process and analytical development, extensive cell culture experience, statistical process control methodologies, statistics, data analysis, and is excited to take on new challenges in a fast-paced and dynamic environment. Additionally, the Process Development Associate will be involved in donor characterization efforts, evaluating efficacy of CAR T cells in animal models, and may assist in the drafting of SOPs and production batch records of ongoing process changes. This is a contractor position reporting to the Senior Process Engineer, MSAT. This position is located at our headquarters in San Diego, CA. | 08/21/2024 |
| 2659 | Presage Biosciences Seattle, WA Histology Research Associate Bachelor’s degree (or equivalent experience) in Biology, Biochemistry, or related field Exp: 1-2 years |
We are seeking a highly motivated individual to join the histology team at Presage Biosciences, an innovative Seattle biotech start-up focused on improving cancer drug efficacy. Reporting to the histology manager you will perform routine histology tasks including specimen processing, embedding, microtomy, staining, and immunohistochemistry. This full-time role supports the development of a cutting-edge target validation and drug evaluation platform. | 08/21/2024 |
| 2660 | Profluent Berkeley, CA Associate Engineer, High Throughput Operations BS/MS in science or engineering discipline Exp: 0-2 years |
We are currently seeking a creative, passionate, and detail-oriented Associate Engineer to join the High Throughput Operations team. The focus of this role will be to develop and implement automated workflows for our in-house molecular cloning core, high throughput screening core, and NGS core. This candidate will work collaboratively with scientists, engineers, and bioinformaticians to develop a suite of assays for measuring gene editing activity and specificity. This is an excellent opportunity to shape the future of AI-driven protein design and to work cross-functionally with a diverse team of experts across machine learning, protein engineering, cell biology, and gene editing. | 08/21/2024 |
| 2661 | Promis Diagnostics Irvine, CA Laboratory Technician BS in Biology, Chemistry, or other medical-related sciences Exp: Entry level |
The Laboratory Assistant or Technician will follow the guidelines set by CLIA and the CA Business and Professional Code of Regulations (BPC: 1212 and 1269) for unlicensed laboratory personnel. Accessions and processes samples (pre-analytical) and prepares samples for testing. Assists CLSs with Preventative Maintenance procedures. Assists CLSs in Quality Control performance, troubleshooting, and in the preparation & storage of reagents. Assist in gathering Calibration and QC data for the CLS to approve before the release of any patient results. Records temperatures and humidity readings as well as other environments. Prepares, orders, and maintains reagents and supplies as required. Ensure that reagents are not used past their expiration date. Documents dating directly on reagents as required by CLIA. Assist QA Manager with QA activities, such as gathering monthly QC reports and assuring the proficiency testing binder is compiled correctly. Provides technical support to clients for our testing services. Will work in partnership with the scientific team in developing and validating new Epigenetics/Genetics tests, including cancer/tumor markers and other inherited disease-related genetic tests. Will collaborate with the scientific and testing personnel team to develop and validate new Molecular Infectious Disease Diagnostic tests for patient care using Real-Time PCR technology. Performs high-complexity laboratory testing in molecular diagnostics, including pharmacogenetics, personal diagnostics, infectious disease, tumor markers, and other molecular testing. | 08/21/2024 |
| 2662 | ProPharma Raleigh, NC Clinical Research Associate (Rare Disease) Bachelor's degree Exp: 0-3 years |
The Clinical Research Associate position is responsible for clinical monitoring for assigned protocols and investigational sites as well as ensuring that studies are conducted and documented in accordance with the study protocol, standard operating procedures, Good Clinical Practices (GCP) and other applicable regulatory requirements. | 08/21/2024 |
| 2663 | PSC Biotech Pomona, CA CQV Project Engineer I Bachelor's degree in relevant engineering discipline Exp: 1-3 years |
We are hiring an entry-level CQV Engineer. Candidates should have prior experience whether through internships or other related professional experience supporting C&Q and GDP/GMP technical documentation. | 08/21/2024 |
| 2664 | PSC Biotech Englewood, NJ Commissioning, Qualification, Validation Engineer I (CQV) Bachelor's degree in relevant engineering discipline Exp: 1-3 years |
We are hiring an experienced CQV Engineer I to support the commissioning, qualification, and validation for a range of equipment and systems within the pharmaceutical and/or medical device industry. | 08/21/2024 |
| 2665 | Psomagen Inc. Rockville, MD NGS Laboratory Technician/Scientist/Manager Bachelor’s degree in biology or relevant major are required Exp: 1 year |
Operate a computer-based laboratory system, record data, and perform laboratory tests. Perform experimental procedures using molecular biology techniques such as isolation of DNA/RNA, Quantification, NGS library construction, qPCR, operating sequencers, micro pipetting, and meticulous measuring. Prepare solution, reagents, and stains by adhering to standard laboratory formulas and procedures. Oversee equipment performance and maintenance schedules. May perform routine repair or replacement of standard parts. Monitor inventory levels, order materials, and supplies in accordance with the established policies and procedures. Troubleshoot problematic samples and results. Communicate effectively with clients and co-workers to improve the existing processes. Adapt to new services/technologies to enhance sales. Train and guide new team members and subordinates. Write and update protocols that meet the CLIA/CAP/ISO standard | 08/21/2024 |
| 2666 | PTC Therapeutics Bridgewater, NJ Research Associate II, Formulation Development Bachelor’s degree in material science, chemistry, chemical engineering or other related scientific discipline Exp: 1 year |
The Research Associate II, Formulation Development contributes to the drug discovery and drug product development process by developing and supporting formulations for preclinical and clinical evaluation and performing pre-formulation characterization studies to support drug product formulation development. This position works cross-functionally with internal departments and external resources on formulation support related issues. The Research Associate II, Formulation Development supports adherence to relevant sound scientific lab practices, regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 08/21/2024 |
| 2667 | PTC Therapeutics Warren, NJ Clinical Operations Assistant Bachelor’s Degree Exp: 1 year |
The Clinical Operations Assistant provides administrative and project support to the Clinical Operations organization. This includes, but may not be limited to, proactively and independently identifying, coordinating, and monitoring the administrative aspects of the departments’ projects/programs and interacting with key stakeholders as necessary; identifying and implementing/supporting administrative systems, processes and procedures; and completing varied routine, ad-hoc and project-driven administrative tasks as assigned. The Clinical Operations Assistant supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 08/21/2024 |
| 2668 | Q² Solutions Durham, NC Immunoassay Associate Scientist Bachelor’s degree in chemistry or a related field Exp: 1 year |
We are seeking an Immunoassay Associate Scientist to join Q² Solutions, IQVIA’s laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Immunoassay Associate Scientist, you will execute laboratory experiments with precision, contribute innovatively to scientific procedure design, and uphold the highest standards of Good Laboratory Practices (GLP) for our clients. You’ll not only set up and conduct experiments but also manage laboratory equipment, ensuring protocols are meticulously followed under the guidance of a dedicated lab services manager, researcher, or scientist. | 08/21/2024 |
| 2669 | Q² Solutions Durham, NC Associate Immunoassay Scientist Bachelor’s degree in chemistry or a related field Exp: 1 year |
We are seeking an Immunoassay Associate Scientist to join Q² Solutions, IQVIA’s laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Immunoassay Associate Scientist, you will execute laboratory experiments with precision, contribute innovatively to scientific procedure design, and uphold the highest standards of Good Laboratory Practices (GLP) for our clients. You’ll not only set up and conduct experiments but also manage laboratory equipment, ensuring protocols are meticulously followed under the guidance of a dedicated lab services manager, researcher, or scientist. | 08/21/2024 |
| 2670 | Q² Solutions Austin, TX Associate Scientist, Assay Development Bachelor's degree in relevant scientific discipline. Exp: 1 year |
We are seeking an Associate Scientist, Assay Developmentto join Q² Solutions, IQVIA’s laboratory business in Austin, TX. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Associate Scientist, you will be responsible for maintaining acceptable and accurate levels of raw and batched inventory in support of reagent manufacturing and production testing. | 08/21/2024 |
| 2671 | Q² Solutions Ithaca, NY Associate Scientist, Sample Preparation Bachelor’s Degree Exp: 1 year |
We are seeking an AssociateScientist, Sample Prepto join Q2 Solutions, IQVIA’s laboratory business atIthaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Scientist, Sample Prep, you will be responsible for sample preparation duties, including troubleshooting routine experiments, preparing solutions and reagents, and driving process improvements. You will also play a key role in training junior level staff. | 08/21/2024 |
| 2672 | Q² Solutions Durham, NC Associate Scientist Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology. Exp: 6 months |
We are seeking an Associate Scientist to join Q² Solutions, IQVIA’s laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Associate Scientist will be instrumental in conducting and documenting analytical procedures, ensuring compliance with SOPs and regulatory guidelines, and contributing to the advancement of our laboratory operations. | 08/21/2024 |
| 2673 | Q² Solutions Durham, NC QC Specialist Bachelor’s Degree in medical technology or equivalent. Exp: 1 year |
We are seeking a Quality Control Specialist to join Q2 Solutions, IQVIA’s laboratory business at Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Quality Control Specialist, you will be responsible for supporting lab quality control processes and improvements, ensuring accuracy and compliance with regulations and SOPs. | 08/21/2024 |
| 2674 | Q² Solutions Ithaca, NY Scientist, Lab Operations Bachelor’s Degree in applied/laboratory sciences with direct laboratory coursework. Exp: 0-2 years |
We are seeking aScientist Laboratory Operationsto join Q2 Solutions, IQVIA’s laboratory business atIthaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Responsible for the accurate execution of laboratory experiments and contributing to the design of scientific procedures. This position aids in the development of scientific discovery and supports Good Laboratory Practices (GLP) for the customer. | 08/21/2024 |
| 2675 | QIAGEN Beverly, MA Finished Goods Formulation Technician II Bachelor’s of Science degree Exp: 1+ years |
The Finished Goods Formulation Technician II formulates buffers, diluents, and PCR master mixes for the Finished Goods team. This position is charged with adhering to the Quality System to execute consistent processes that result in repeatable product for on time delivery. | 08/21/2024 |
| 2676 | Quality Agents Rockville, MA Validation Engineer I BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by the client. | 08/21/2024 |
| 2677 | Quanta Therapeutics Radnor, PA Research Associate/Sr. Research Associate BS/MS in cancer biology/molecular/cell biology or related biomedical field Exp: 1-3 years |
A highly motivated, detail-oriented, hands-on biologist to contribute to existing programs and to initiate and develop new drug discovery efforts within Quanta. The ideal candidate will have a good understanding of cancer biology, signal transduction pathways, and hands-on experience in elucidating molecular mechanisms underlying tumorigenesis. He/she will work with a collaborative team and contribute to the Company’s pipeline. | 08/21/2024 |
| 2678 | QuidelOrtho Raritan, NJ Quality Control Scientist I Bachelor’s degree in medical technology, Biology, Chemistry or a related field of study Exp: 1-3 years |
As the company continues to grow as QuidelOrtho, we are seeking a QC Scientist I. The QC Scientist I will be responsible for testing stability and final product release of all OCD products. This person will assure compliance with company standards and applicable regulatory agencies. They will participate in failure investigations to help determine root cause, track and trend data, identify and suggest process improvements to improve business measures. This position will be onsite full-time at our Raritan, NJ office. | 08/21/2024 |
| 2679 | QuidelOrtho Athens, OH Associate Biochemist Bachelor’s Degree in a biology, biochemistry, chemistry or other related science field Exp: 1 year |
The Associate Biochemist is responsible for the production and quality testing of various raw material, intermediate components and finished good catalog items, in accordance with Quidel’s Quality System Regulations. This role is located in Athens, Ohio. | 08/21/2024 |
| 2680 | QuidelOrtho Athens, OH Quality Engineer B.S. Degree in Chemistry, Biochemistry, Biology, Engineering, or a related discipline. Exp: 1-3 years |
The Quality Engineer provides support to Quality and Operations on all aspects of the manufacturing process. The position will work to resolve quality issues by ensuring adequate root cause investigations conducted and verifying effectiveness of CAPAs implemented. The position will utilize key Quality Engineering principles, tools, and practices to develop and optimize process controls and quality system processes and identify opportunities to improve quality and cost that are aligned with the overall business goals and QuidelOrtho’s Quality Policy. The position will assess risk and will drive quality related decisions. This role is located in Athens, Ohio. | 08/21/2024 |
| 2681 | QuidelOrtho Athens, OH Associate Molecular Biochemist BA/BS or MA/MS in life sciences-related field. Exp: 1-3 years |
The Associate Molecular Biochemist plays a crucial role in GMP molecular chemistry production and in-process quality testing activities. Responsibilities include molecular biochemistry production and quality testing. The Associate Molecular Biochemist will perform routine procedures with senior staff oversite. Some collaboration with senior staff on investigations and troubleshooting is expected. This role is located in Athens, Ohio. | 08/21/2024 |
| 2682 | Quintara Discovery Hayward, CA Senior Research Associate Master’s degree in Biology or related field. Exp: 1 year |
Responsible for exercising independent judgment in conducting research on in vitro ADME screening (ADME: Absorption, Distribution, Metabolism, and Elimination): Plan experimental approaches; Design and carry out bioanalytical tests of various compounds for the potential development of human therapeutics; Analyze and interpret experimental data and prepare reports of findings. Design and perform procedures in ADME assay projects by operating lab equipment, including integrated hardware, software, optical and fluidic subsystems; Conduct sample bioanalysis and develop bioanalytical methods for the quantitative analysis by using mass spectrometry; Document information on procedures, modifications, and methods; maintain records of experiments and results in the accessible format. | 08/21/2024 |
| 2683 | Quotient Sciences Boothwyn, PA Validation Engineer ??Bachelor’s degree in Engineering, Information Systems, or a related field of study preferred Exp: 0-5 years |
The Validation Engineer is responsible for providing engineering support for maintenance and validation activities while managing regulatory requirements around methodology and protocols for pharmaceutical manufacturing. | 08/21/2024 |
| 2684 | Qx Therapeutics New Haven, CT Scientist 1 Bsc, or Msc degree in a biological/pharmacology discipline. Exp: 0-5 years |
This is an opportunity to work on cutting edge science to tackle diseases related to acute lung injury. We are looking for a scientist who brings enthusiasm, intellectual curiosity, scientific rigor and a desire to innovate new medicines for patients. Assume responsibility for in vivo studies to advance our lead development programs, including study planning, protocol design, study execution, data analysis and study report writing. Implement good documentation practices. Manage in vitro biological assay development and execution. Manage in vivo model development and characterization. Analysis of experimental data and draft study report. Effectively collaborate with a fully integrated team to facilitate the success of projects. Assume part of project management work for the organization. | 08/21/2024 |
| 2685 | Bio-Techne Minneapolis, MN Research Associate, Protein Purification GMP Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 08/21/2024 |
| 2686 | Bio-Techne San Marcos, CA Chemistry Associate Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 years |
By joining Bio-Techne, San Marcos you’ll join a proven leader in the Manufacturing of In-Vitro Diagnostics. Our Research Associates are focused on the product development of diagnostic assays, to include reagents, calibrators, controls, calibration verifiers and proficiency testing. When you join us, you will be part of a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all its brands, provides tools for researchers to further treat and prevent disease worldwide. Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology, and practices that apply to manufacturing in a laboratory environment. | 08/21/2024 |
| 2687 | Nova Biomedical Waltham, MA Quality Engineer I BS degree in engineering, the sciences, or another technical discipline. Exp: 1-2 years |
Nova Biomedical is hiring a Quality Engineer I on-site (hybrid) in our Waltham, MA facility. This role will support Quality Assurance activities within the corporate Quality Management System (QMS). Responsibilities include providing expertise and general oversight for the management and improvement of design and development, validations, quality planning, internal auditing, investigations, process controls, change management, quality records, corrective and preventive activities, data management, employee training, and other duties as assigned. | 08/06/2024 |
| 2688 | Novartis San Diego, CA Research Scientist - In Vitro Pharmacology B.S. in molecular biology, cell biology, biochemistry, bioengineering, or related scientific discipline Exp: 0+ years |
We are seeking a highly skilled and motivated Research Scientist I to join our dynamic in vitro pharmacology team In San Diego dedicated to advancing gene therapy and siRNA for neurological and neuromuscular diseases. As a key member of our research team, you will play a critical role in supporting various aspects of research including tissue sample processing, biodistribution, biomarker assay development, antibody screening campaigns, as well as oversee lab operation activities. Join us in our mission to transform the treatment landscape for neurological and neuromuscular diseases through cutting-edge gene therapy approaches. Apply now to make a meaningful impact on the lives of patients worldwide! | 08/06/2024 |
| 2689 | Novasenta Pittsburgh, PA Research Associate, Assay Development Master’s Degree or bachelor’s degree from an accredited institution Exp: 1+ years |
Conducts routine and non-routine lab procedures and assays for molecular, cellular, and metabolic characterization of relevant samples from mouse models of cancer and human clinical cancer tissue. This includes the conduct of relevant exploratory experiments and control experiments, applying basic scientific principles. As needed, supports the development and validation of new technologies for molecular, cellular and metabolic characterization of samples. Supports the development of biological, immunological assays to investigate mechanisms of immune-mediated effects of novel identified targets. Contributes to the profiling and validation of novel, druggable, immunotherapy targets. Documents and maintains a detailed and precise record of work performed. Performs lab management, which includes ordering supplies and maintaining inventory, ensuring safety, service and maintain laboratory instruments of the lab,etc. Atively participates in the scientific dialogue of the group and proactively collaborates with colleagues. Performs all other duties as assigned | 08/06/2024 |
| 2690 | Novavax Gaithersburg, MD Research Associate II Bachelor’s or Master’s degree in Immunology/Virology or relevant field Exp: 1+ years |
We are seeking a highly motivated individual to serve as a Research Associate who takes on the responsibility in support of study projects on cellular assays for Adjuvant and Vaccine candidates. This position will require the incumbent to develop and qualify assays for analyzing samples from preclinical and clinical studies, mainly by using Flowcytometric staining, but can extend to other cellular assays such as Elispot and cytotoxicity assay. This position will mostly involve hands-on laboratory work. | 08/06/2024 |
| 2691 | Novavax Gaithersburg, MD Research Associate II - Vaccine Immunology B.S. or M.S. in Immunology, Biology, Molecular Biology, Virology, Genetics or related field. Exp: 1+ years |
Novavax, Inc (Nasdaq:NVAX) is a biotechnology committed to helping address serious infectious diseases globally through the discovery, development and delivery of innovative vaccines to patients around the world. We have more than a decade of experience contending with some of the world’s most devastating diseases, and we are here to make a difference. Hard-won lessons and significant advances illustrate that our proven technology based on solid science tested by decades of research, has tremendous potential to make a substantial contribution to public health worldwide. | 08/06/2024 |
| 2692 | Novavax Gaithersburg, MD Analytical Development Associate I/II (Contract) Bachelor’s degree OR Master’s degree Exp: BS: 1-2 years or Master's: Some industry internshnip or co-op exp |
Novavax is seeking an Associate II, Analytical Development to provide technical and documentation support in a laboratory setting. This role is responsible for contributing to the method development, qualification, and technology transfer for analytical methods. The qualified individual will bring experience in relevant analytical technologies, such as ELISA, SRID, Luminex, or BLI. The position will perform in-process testing, as needed, to support the Process Development, Formulation Development, and Manufacturing teams, in addition to method development and qualification. | 08/06/2024 |
| 2693 | Novitium East Windsor, NJ Specialist Preventive Maintenance Bachelor’s in Instrumentation / industrial / electronics / electrical / mechanical / related Exp: 6+ months |
Responsible for developing and carrying out a scheduled preventive maintenance program for plant utilities and manufacturing equipment; Troubleshoot existing equipment for issues, change or modify to improve efficiency; Work closely with EHS to maintain facility compliance with applicable OSHA and DEP regulations; Prepare and assist Plant Shut-Down plans and coordinate with all departments to execute the plans; Develop, maintain, and oversee Spare Parts Inventory system and its procurement in collaboration with Purchasing Manager; Manage the organization and maintenance of spare parts warehouses and workshops; Set in service for an existing system to manage Work Orders; Discuss heating/cooling system malfunctions with users to isolate problems or to verify that problems have been corrected; Record and report all faults, deficiencies and other unusual occurrences as well as time and materials expended on work orders. | 08/06/2024 |
| 2694 | Novitium East Windsor, NJ Regulatory Specialist Bachelors in Pharmaceutical sciences / biology / microbiology / chemistry / chemical / Regulatory Affairs Exp: 1+ years |
Review, manage and write regulatory submissions electronically which include New ANDA filings, Complete Response letters, Information requests, Amendments to the ANDA’s (Labeling, Chemistry & Bioequivalence) of different dosage forms (Tablet, Capsule, Liquid & Solutions); responsible for filing the Post Approval Supplements like CBE-0, CBE-30 (Changes being effective in 30 days) and Prior Approval Supplements (PAS); submitting dossiers electronically after the approval of initial product submissions (ANDA); review of the leachable and extractable reports generated for the oral Liquid & Solution drug products. | 08/06/2024 |
| 2695 | Novitium East Windsor, NJ Sr. Software Engineer Master’s in computers / electronics / electrical / related Exp: 6+ months |
Design and implement Netapp storage systems, including installation, configuration, software upgrades, and storage provisioning; deploy NetApp tools (OCUM,WFA,DFM,snapcreator) to support production operation; configure ifgroups, IPSapce, Vlan’s and Braodcast domains; administer Fiber Channel SAN fabrics, including installation, configuration, zoning, software upgrades, and maintenance of switches; responsible to code and maintain system scripts to support operations of the storage systems; perform architectural planning, designing, coding, and prepare test plans; deploying & configuring new virtual systems and ecosystems. | 08/06/2024 |
| 2696 | Novitium East Windsor, NJ Instrumentation Engineer Bachelor’s in Instrumentation / industrial / electronics / electrical / mechanical / related Exp: 6+ months |
Responsible for Instrument and Equipment’s of entire Plant; Installation, troubleshooting & calibration of instruments such as TOC Analyzer, HMI, PLC, Flow Meters, Temperature controller, transmitter, pressure transmitter, gas analyzer; Maintaining minimal instrument downtime through troubleshooting & maintenance activities; Maintaining data backup, instrument documentation, and Spares Inventory & Annual Maintenance contracts; Pro-active Support for Quality Control, Production & Compliance group’s activities; Follow-ups and closures of instrument Change controls, deviations instrument related incidents, & CAP A (corrective and preventive action); Procurement of qualified equipment’s as per GLP & Pharmacopeia requirements, and responsible for IQ, OQ, DQ and PQ for instruments and manage all paperwork. | 08/06/2024 |
| 2697 | Novitium East Windsor, NJ Quality Control Analyst Bachelors in Pharmaceutical Sciences / Biology / Chemistry / Microbiology / Chemical / Related Exp: 1+ years |
Conduct research, analysis, synthesis, and experimentation on substances, for such purposes as product and process development and application, quantitative and qualitative analysis, and improvement of analytical methodologies; conduct testing and analysis of pharmaceutical raw materials like drug substance, excipients and packaging materials to analyze various parameters like assay, dissolution, impurities, related substances, residual solvents using various technical instruments like HPLC, GC, UV spectrometry; Conduct testing and analysis of finished product for different dosage forms like capsules, tablets, powder for oral suspension and solutions. The dosage forms include food supplements like vitamin capsules, mineral tablets, and multivitamin syrups. | 08/06/2024 |
| 2698 | OraSure Technologies Bethlehem, PA Formulations Specialist Bachelor of Science in chemistry, biochemistry, or equivalent sciences Exp: 1-3 years |
The formulations specialist manufactures chemical formulations necessary for production of finished goods, documents production information, and performs routine maintenance on equipment/machinery. | 08/06/2024 |
| 2699 | Novonesis Wausau, WI Process Engineer Bachelor of Science degree in Engineering Exp: 1-3 years |
This position works under general direction and is primarily responsible for developing and improving manufacturing processes by studying product and manufacturing methods. The Process Engineer is responsible for commissioning manufacturing equipment and ensuring equipment operates and performs as intended. | 08/06/2024 |
| 2700 | Novonesis Franklinton, NC Process Engineer I BS or MS in Engineering Exp: 0+ years |
You will have the opportunity to work closely with production to ensure things operate smoothly and efficiently. You will be able to drive process improvements, work with capital projects, and support upscaling new processes from development. | 08/06/2024 |
| 2701 | Noxilizer Hanover, MD R&D Lab Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1+ years |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 08/06/2024 |
| 2702 | Globus Medical West Carrollton, OH Associate Engineer, Manufacturing Bachelor's Degree in Electrical Engineering Exp: 0-2 years |
As part of the manufacturing team, the Associate Manufacturing Engineer needs to have strong technical skills, be hands-on, and be creative with minimum supervision. The job requires a team player with the ability to function well in a challenging, fast-paced environment. This person must be enthusiastic, positive, even-tempered, and have strong skills in areas of communication, dependability, interpersonal relationships, flexibility, and maturity. | 08/06/2024 |
| 2703 | Ocular Therapeutix Bedford, MA Microbiology Analyst I B.S. degree in Microbiology, Biology or related scientific field. Exp: 1 year |
The Microbiology Analyst I is responsible for performing QC activities in microbiology lab such as Environmental Monitoring of the cleanrooms and support in performing testing of product and raw materials according to established specifications and procedures. This position also manages EM excursions and data entries. | 08/06/2024 |
| 2704 | Ofni Systems Raleigh, NC Computer Systems Validation Engineer BS or equivalent degree in math, science or engineering Exp: 1 year |
We are hiring a Validation Engineer to be on the cutting edge of automated validation techniques. You will be responsible for implementing our validation solutions while working with industry-leading companies. Ideal candidates are experts on the requirements of 21 CFR 11, have excellent critical thinking and interpersonal skills, and are motivated to meet client needs for compliance. If you are an A-level engineer who enjoys the challenge of solving real-world compliance problems then we would like to talk with you. | 08/06/2024 |
| 2705 | OncoPep Cambridge, MA Research Associate (In Vitro) BS Exp: 1 year |
We are looking to expand our Research team by recruiting a skilled Research Associate in cellular/molecular biology to join our growing team. The candidate will primarily work with molecular and cell biology techniques including culture of primary cells and cell lines, flow cytometry, ELISA, and western blot. He/She will play an important role in the discovery and development of novel biotherapeutics for immuno-oncology. He/she will be responsible for generating the tools necessary for evaluation and screening of lead candidate therapeutics. He/she will be expected to participate in experimental design, conduct experiments, optimize throughput, maintain detailed records, and generate standard operating procedures. | 08/06/2024 |
| 2706 | Orbital Therapeutics Cambridge, MA Research Associate, Molecular Immunology B.S. or M.S. in Immunology, Biology, or related field. Exp: 1-4 years |
Orbital Therapeutics is currently seeking a highly motivated, self-driven, and creative individual with extensive experience in molecular immunology, looking to join an outstanding research team dedicated to designing and executing studies using a new generation of RNA medicines. This individual will enjoy working in a pioneering, fast-paced, and collaborative start-up environment with the opportunity to coordinate studies focused on immunomodulation, while also exploring ways to unleash the power of Orbital’s core technologies. This individual will join a culture of intellectual rigor, scientific curiosity, and collegiality, cross functionally contributing to research across the organization. The candidate will be an important team member whose contributions will be critical to our success in developing new therapeutics to improve the lives of patients. | 08/06/2024 |
| 2707 | Organogenesis Norwood, MA QC Analyst I-Cell Culture Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Cell Culture performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. The QC Analyst I performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 08/06/2024 |
| 2708 | Organogenesis Norwood, MA QC Analyst I - Chemistry Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Chemistry performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. Performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 08/06/2024 |
| 2709 | OriGen Biomedical Austin, TX Quality Engineer I Bachelor’s degree in Engineering Exp: 1-2 years |
The Quality Engineer I is responsible for technical duties within the Quality organization including validation and qualification, calibration, and customer contact. These duties will support manufacturing operations, customer service, process improvement, and regulatory requirements. | 08/06/2024 |
| 2710 | Packgene Biotech Houston, TX Quality Control Specialist I - HPLC Bachelor's degree in bioscience, chemistry or related field Exp: 1-2 years |
The Quality Control Specialist I or II- HPLC will undertake laboratory work under the guidance of senior scientists. The Quality Control Specialist I or II is responsable to operate and maintain HPLC instruments; execute HPLC assays. The Quality Control Specialist I will have chance to learn Gene Therapy concepts and cGMP practice, etc | 08/06/2024 |
| 2711 | Padagis New Hope, MN QC Chemist II Bachelor's degree Exp: 1+ years |
We are hiring for a QC Chemist II, 2nd Shift, in New Hope, MN who performs inspection on a range of work to detect defects and maintain quality standards. The hours for this role are Monday through Friday 2pm-10pm with some flexibility. | 08/06/2024 |
| 2712 | Endo Rochester, MI Quality Associate Specialist, Product Release (Midnight shift) BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 08/06/2024 |
| 2713 | Endo Rochester, MI Quality Associate Specialist, Product Release (Days) BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 08/06/2024 |
| 2714 | Endo Horsham, PA Quality Associate Specialist, MQA BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, under close supervision, performs routine collection of environmental and utility monitoring samples. This role also reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. May participate in “on the floor” activities during product manufacturing. | 08/06/2024 |
| 2715 | Paradromics College Station, TX Preclinical Research Assistant Bachelor’s or Master’s degree in Science or Engineering Exp: 1+ years |
The Paradromics Neuroscience team is seeking strongly motivated Research Assistants to contribute to the preclinical testing of our Connexus® Direct Data Interface in large animal models. This role is a temporary position with a fixed period of a year with the possibility of renewal at the end of the contract. This role involves interfacing with veterinarians, neuroscientists, electrical engineers, software engineers, and data engineers. Excellent communication and interpersonal skills are crucial for excelling at this role. This role requires an individual with a “can-do,” self-starter attitude. This position is based on-site in College Station, Texas. We are building next-generation brain implants to treat serious conditions in mental and physical health. If you want to use your skills in a positive, impactful way, if you like to be intellectually challenged, and if you want to be surrounded by hard-working and passionate co-workers, this work will be highly fulfilling. | 08/06/2024 |
| 2716 | Paragon 28 Englewood, CO Associate Quality Engineer - Rotational Bachelor’s in engineering or technical discipline Exp: 0-2 years |
The Rotational Associate Quality Engineer has varied responsibilities to assist both the Quality-Production and Quality-Design teams in ensuring Paragon 28’s compliance to regulations and standards. The role will split time and/or rotate through day-to-day tasks and exposure to the supplier quality engineering, design quality engineering and production quality engineering roles at Paragon28 for a 12-month period, with the intention of aligning a candidate’s skills and passion with business needs for permanent placement within the quality department | 08/06/2024 |
| 2717 | PCI Pharma Philadelphia, PA Process Engineer-AM Weekends Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout. **This is a weekends position. Friday, Saturday, & Sunday 7am to 7pm.** | 08/06/2024 |
| 2718 | PCI Pharma Philadelphia, PA Process Engineer I-2nd Shift Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout. *This is a 2nd shift position. The hours are 3pm to 11pm, Monday to Friday. | 08/06/2024 |
| 2719 | PCI Pharma San Diego , CA QA Specialist - Sterile Fill & Finish Bachelor’s degree Exp: 1-2 years |
This full-time position will report to the Quality Manager - Sterile Fill Finish focusing on supporting the Quality department with review and release of executed batch records, product inspection, product or raw material release, document control, production monitoring, environmental monitoring, tracking quality metrics and assisting with validations, preventative actions, audits and continuous improvement. This position is responsible for performing quality activities within the Sterile Fill and Finish group in accordance with all applicable procedures, regulations, and safety directives. This individual’s primary job function will be review and release finished lots of drug product vials and syringes manufactured by PCI. Other job functions may be required at the discretion of management and include but are not limited to drafting procedures, sampling raw materials or finished products, assisting in general operations of the zero human intervention isolators all in accordance with GMPs and established SOPs | 08/06/2024 |
| 2720 | Pel-Freez Biologicals Rogers, AR Quality Control Technician Bachelor's degree in science Exp: 1 year |
Under supervision, the QA Technician I will perform quality control testing and assist with the implementation of the Pel-Freez quality management system in accordance with ISO 9001. The role will be required to understand and promote the Quality System as part of the Company's overall goal toward continual improvement through strict adherence to all company policies, procedures, principals, and values. | 08/06/2024 |
| 2721 | Penumbra Alameda, CA Manufacturing Engineer II BS degree in Mechanical, Biomedical, Chemical, or Materials Engineering, or a related discipline required Exp: 1+ years |
As a member of the Manufacturing Engineering group at Penumbra, you will be called upon to solve complex problems and implement innovative solutions. You will provide manufacturing technology and robust solutions aimed at commercializing new products and continuously improving production processes. Working cross-functionally with engineering groups across the company, as well as with Production, Quality Control and Quality Assurance, you will resolve problems encountered on the production floor and throughout the business, and will apply your engineering knowledge and creativity to implement adaptations and modifications to the production line and to quality systems. | 08/06/2024 |
| 2722 | Penumbra Alameda, CA Manufacturing Engineer II BS degree in Mechanical, Biomedical, Chemical, or Materials Engineering, or a related discipline required Exp: 1+ years |
As a member of the Manufacturing Engineering group at Penumbra, you will be called upon to solve complex problems and implement innovative solutions. You will provide manufacturing technology and robust solutions aimed at commercializing new products and continuously improving production processes. Working cross-functionally with engineering groups across the company, as well as with Production, Quality Control and Quality Assurance, you will resolve problems encountered on the production floor and throughout the business, and will apply your engineering knowledge and creativity to implement adaptations and modifications to the production line and to quality systems. | 08/06/2024 |
| 2723 | Penumbra Alameda, CA Quality Engineer I Bachelor’s or Master's degree in an engineering or scientific discipline required Exp: 1+ years |
As a Quality Engineer I, you will be charged with the quality behind Penumbra's game-changing medical devices used to address some of the world's toughest disease states! Unlike quality engineering roles in other companies, at Penumbra, we provide our quality engineers with highly technical problems to solve. Your efforts will directly impact the safety of patients around the world who use our products. You will apply your passion for creative problem solving throughout all stages of the process, from concept to commercialization and into continuous improvements. | 08/06/2024 |
| 2724 | Performance Validation Grand Rapids, MI Level I/II Validation Engineer/Specialist BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering Exp: 1+ year |
Performance Validation is seeking a full-time Level I or Level 2 Validation Engineer/Specialist to join our team in Grand Rapids, Michigan. Level I/II Validation Engineer/Specialist reports directly to the Division Director or Manager and will be assigned to one or more project teams headed by a Project Leader. | 08/06/2024 |
| 2725 | Pfizer Pearl River, NY Associate Scientist– Viral Vaccines & Immunology Bachelor's Degree in a relevant field of science Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support the preclinical evaluation and early clinical development of mRNA and protein based viral vaccines. You will perform various assays to monitor the immune responses elicited by respiratory virus, herpesvirus, and influenza virus vaccine candidates. In addition, you will maintain cell lines and prepare preclinical and early clinical samples for testing. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. Your strong work ethic and collaborative spirit will be an integral part of our dynamic team. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 08/06/2024 |
| 2726 | Pfizer Pearl River, NY Associate Scientist - Sample Logistics and Solutions Bachelor of Science Degree or Bachelor of Arts Degree in a relevant scientific discipline Exp: 0-5 years |
The primary purpose of this job role is to function as a member of the Sample Logistics and Solutions (SLS) team within Pfizer Vaccine Research and Development (VRD). The incumbent will be responsible for receiving samples from global clinical/study trials according to approved protocols and processes. The individual will participate in all aspects of tracking and documenting the chain of custody of samples. The incumbent’s role will include sample receipt, documentation, storage, tracking, aliquoting, distribution to the testing labs, and sample disposal. The colleague will work in a team setting and will share roles and responsibilities as assigned by the team leader/manager. | 08/06/2024 |
| 2727 | NAMSA Northwood, OH Microbiology Technologist Bachelor Degree Exp: No Experience |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions, Accurately collects and records raw data in logbooks and on worksheets, May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures, May be required to perform required specific testing as applicable, May be required to operate specified laboratory equipment, May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable), Other duties as assigned. | 07/17/2024 |
| 2728 | NAMSA Minneapolis, MN Associate Pathology Technician Bachelor degree or equivalent in Biological Sciences or related discipline Exp: 0-2 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: Supports or independently performs necropsy procedures, including complete necropsies and perfusion procedures. Assists and performs routine gross examination as required by GLP standards, and performs accurate and timely record keeping. Assists in coordinating and performing the shipping of all pathology related specimens to the appropriate designated facility. Performs thorough recordkeeping of shipping and receipt logs. Performs tissue trimming according to established guidelines. Performs photography and high-resolution x-ray imaging and film developing. Maintains proficiency in all appropriate designated departmental SOPs with knowledge of lab processes. Assists in the review of protocols that include pathology services, and assists with modifying pathology-related SOP’s. Maintains a clean, GLP-compliant lab and ensures all logbooks are reviewed and correct. Maintains laboratory equipment according to applicable SOPs. Performs calibration or validation activities to specialized equipment. Other duties as assigned. | 07/17/2024 |
| 2729 | NAMSA Minneapolis, MN Associate Pathology Technician Bachelor degree or equivalent in Biological Sciences or related discipline Exp: 0-2 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: Supports or independently performs necropsy procedures, including complete necropsies and perfusion procedures. Assists and performs routine gross examination as required by GLP standards, and performs accurate and timely record keeping. Assists in coordinating and performing the shipping of all pathology related specimens to the appropriate designated facility. Performs thorough recordkeeping of shipping and receipt logs. Performs tissue trimming according to established guidelines. Performs photography and high-resolution x-ray imaging and film developing. Maintains proficiency in all appropriate designated departmental SOPs with knowledge of lab processes. Assists in the review of protocols that include pathology services, and assists with modifying pathology-related SOP’s. Maintains a clean, GLP-compliant lab and ensures all logbooks are reviewed and correct. Maintains laboratory equipment according to applicable SOPs. Performs calibration or validation activities to specialized equipment. Other duties as assigned. | 07/17/2024 |
| 2730 | NAMSA Irvine, CA Senior Lab Technician - Sterility Assurance Bachelor degree Exp: 1 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description:May perform various testing independently in accordance with SOPs and utilizing applicable work instructions, standards or guidelines. Performs routine calculations and may participate in analyzing and interpreting results. Maintain all test equipment and supplies for various testing. Clean glassware and prepare reagents for use in laboratory testing. Perform routine disposal of laboratory waste including disposal of test articles. Assist with making solutions and preparing reagents. Assist in the preparation of items for testing. Monitor raw materials and final finished media for conformance with applicable material specifications and SOPs. May be responsible for extractions, which may include: test article and control preparation, animal holding and preparation and solution preparation. May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. Accurately collect and record raw data in logbooks and on worksheets. | 07/17/2024 |
| 2731 | NAMSA Irvine, CA Associate Microbiologist Bachelor degree Exp: 1 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: Independently perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs, and according to applicable work instructions. Prepare or participate in the preparation of test specifications in conjunction with the requirements of the applicable standards and/or client instructions. May have direct client contact as needed. Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and for taking all concerns to management as required. Accurately collects and records raw data in logbooks and on worksheets. Responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in SOPs. | 07/17/2024 |
| 2732 | Nanomix San Leandro, CA Associate Scientist, Assay Development Bachelor’s degree (or equivalent) in in Biology, Bioengineering, Chemistry, Chemical Engineering, or related field Exp: 0-2 years |
Nanomix has developed tests for the diagnosis of sepsis, acute kidney injury, and COVID-19, and is looking for an Assay Development Associate Scientist to help accelerate these programs and the development of other IVD assay products in the pipeline. This is an opportunity to work with a world class team to deliver an advanced, mobile medical diagnostic platform of urgent need to the healthcare industry. The successful candidate will apply scientific & technical skills in all phases of developing diagnostic assay products. Assist in developing Nanomix eLab biosensor cartridge assays to detect various biomarkers &/or viral/bacterial antigens. | 07/17/2024 |
| 2733 | Element Bend, OR Chemist I/Chemist II Bachelor’s Degree in Chemistry or related field is required. Exp: Some experience (for Chemist I) or 2 years experience (for Chem II) in a laboratory setting |
Element has an opening for a Chemist I or Chemist II position at our extractables and leachables (E&L) testing Center of Excellence in Bend, OR. This position will work in a cGMP-regulated environment under the direction of a Team Lead or other senior staff member in laboratory and office settings. The position will work with a team completing E&L project work using internal methods, protocols and SOPs according to customer specific requirements. This position requires working in a collaborative manner with other team members to accomplish organizational goals, providing ideas to improve efficiency and actively contributing to positive co-worker/customer relationships through efficient interaction on current projects. The Chemist I or Chemist II will also contribute to team continuous improvement initiatives. | 07/17/2024 |
| 2734 | Element Wixom, MI Project Manager - Engineer Bachelor of Science degree in a science or testing related field including but not limited to: Metallurgical Engineering, Materials Science, and Polym Exp: 0-5 years |
Element has an opportunity for an Engineer to join our rapidly expanding Project Management team in our Wixom, MI Lab. The Project Manager will be coached to be able to provide quotations, manage testing programs, write technical reports, and support the other team members. Our Engineers perform a variety of routine and non-routine testing assignments and insures timely and accurate test results under minimal direct supervision. The project manager position must be proficient in a number of core business and technical skills as well as compliance to established safety rules, code of conduct, and company policies and procedures. | 07/17/2024 |
| 2735 | Element Fremont, CA Electromagnetic Compatibility Compliance Engineer Bachelor’s Degree in Engineering Exp: 0-2+ years |
Element, has an opportunity for Electromagnetic Compatibility Compliance Engineer in the Regulatory Division of our Fremont, CA. This position applies engineering concepts for testing and evaluation of electronic and wireless RF devices for US federal and international regulatory compliance. Determining compliance requires the understanding and application of test standards, diagnosing problems, analyzing results, and troubleshooting unexpected performance in a fast-paced environment and industry. All training provided. | 07/17/2024 |
| 2736 | Element Huntington Beach, CA Associate Engineer Bachelor of Science degree in a science or testing related field Exp: 0-1 years |
Join us as an Associate Test Engineer and see how your variety of routine and non-routine testing make a difference and how critical it is to helping us deliver on our purpose and achieve our goals. Element is a world renown Aerospace Testing Company with clients such as Boeing, SpaceX and Blue Origin. At Element our shared purpose of ‘Making tomorrow safer than today’ is what brings us together. We are energized by our ambition to make the world a better place and create a safer future for people. This is what sets us (and you, if you join us…) apart from the crowd. | 07/17/2024 |
| 2737 | NantWorks Culver City, CA Battery Engineer B.S/M.S. in Mechanical Engineering, Chemical Engineering, Materials Science, or related technical field Exp: BS - 2 years; MS - 0+ years |
The Battery Engineer will be responsible for development, selection and validation active materials across the anode and cathode portfolio, assisting in development and implementation of R&D tools, and general engineering tasks. This includes developing and characterizing active/passive materials, developing slurry and coating recipes, building cells, and cell testing, leading engineering design and construction. This individual will be a key contributor in advancing NantG Power's competitive advantage to drive energy density, power density, safety, and materials sustainability improvements at scale. The ideal candidate will have a strong record of scientific achievement in the areas of Li-ion batteries, nanomaterials, and/or electrochemistry. | 07/17/2024 |
| 2738 | LGC Biosearch Technologies Alexandria, MN Quality Control Technician I - Laboratory Bachelor’s degree in a relevant scientific discipline Exp: 0-2 years |
The Quality Control (QC) Technician I focuses on the performance of analytical testing activities within the consumable product lines. They are responsible for testing intermediate and finished products, analysing the results of Quality Control testing and comparing results to established specification and/or customer requirements. In addition, they may perform testing and/or review of incoming goods. | 07/17/2024 |
| 2739 | LGC Biosearch Technologies Cumberland Foreside, ME Manufacturing Chemist I Bachelors degree in life science field or other related science or medical Exp: No Experience |
The Manufacturing Chemist I fulfills the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 07/17/2024 |
| 2740 | LGC Biosearch Technologies Middleton, WI Lab Services Technician Bachelor's degree in a scientific field of study (e.g. biology, chemistry, physics) Exp: 0+ years |
The Lab Services Technician provides foundational support to the processing and preparation of client samples for the Lab Services team at a specific operational site. In agreement with other Lab Services team members, this position is responsible for driving their operational duties by supervisor direction as well as standard operating procedures (SOPs) and work instructions. | 07/17/2024 |
| 2741 | LGC Biosearch Technologies North Charleston, SC Production Chemist I Bachelor of Science degree is required, chemistry degree preferred Exp: 0-2 years |
The Production Chemist I is responsible for the manufacturing of reference standard solutions by following routine procedures and operations of laboratory equipment. This is a highly collaborative position and requires a high level of teamwork and productivity. We are looking for individuals that can thrive in a fast-paced laboratory setting and demonstrate ability to prioritize and organize work with guidance from team leads and supervisor. Our site manufactures both catalog and custom solutions for customers requiring focused bench work, detailed record keeping and flexibility in daily tasks. | 07/17/2024 |
| 2742 | LGC Biosearch Technologies Petaluma, CA Oligonucleotide Production Technician - Liquid Handling Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
The Oligonucleotide Production Technician I will perform tasks associated with the production of modified oligonucleotides in a high throughput time sensitive manufacturing environment in compliance with company procedures and external regulatory requirements. | 07/17/2024 |
| 2743 | Sotera Health Salt Lake City, UT Lab Analyst - Analytical Chemistry Bachelors Degree, relevant Life Science Exp: No Exp |
Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. | 07/17/2024 |
| 2744 | Nemagen Discoveries Newark, NJ Research Scientist B.S. in a Biological Science orin a related field Exp: 0+ years |
NemaGen Discoveries’ mission is to advance therapies to treat mast cell-related and chronic inflammatory diseases. Under the direction of NemaGen’s Principal Scientist, you’ll work in an exciting and fast-paced start-up environment where you’ll assist with the development of NemaGen’s research programs. NemaGen is looking for candidates with a strong scientific background that have an interest in entrepreneurship and helping grow NemaGen in the coming years. If you want to be a part of cutting-edge research and improve the lives of patients, we encourage you to apply! Design and perform cell culture assays related to the development of innate immune cells with novel chemical compounds. Phenotypically and functionally characterize the activation state of various immune cell populations. Perform in-vitro efficacy studies. Operate standard laboratory equipment including, but not limited to, centrifuges and flow cytometers. | 07/17/2024 |
| 2745 | AstraZeneca Santa Monica, CA Associate, Quality Control Analyical BS in biological sciences or a related field is required. Exp: 0+ years |
Neogene is looking for an energetic and experienced person with cell therapy quality control background to join our Quality Control (QC) team. You will contribute to the advancement of our product pipeline by performing QC analytical method qualification, complete sample analysis and other assigned tasks. You will also independently organize and present results and conclusions. You will ensure that the QC Analytical laboratory is operating as expected. | 07/17/2024 |
| 2746 | NeoGenomics Laboratories Durham, NC Molecular Laboratory Technologist, Temporary Bachelor’s Degree in one of the chemical, physical, or biological sciences Exp: 1+ years |
The Laboratory Technologist works under minimal supervision and consistently and independently performs the complex level of clinical tests by following department procedures. You will drive initiative for prompt, accurate performance of test results with appropriate documentation of result. | 07/17/2024 |
| 2747 | Neolight Scottsdale, AZ Biomedical Engineer Bachelor's or Master's Degree in Electrical Engineering Exp: No Experience |
We seek a full-time entry-level Biomedical Engineer focusing on Electrical Engineering. In this role, you will provide strong, independent technical support to teams that contribute to resolving significant electrical and embedded system issues for the next generation and on-market products. A successful candidate will be a productive individual contributor who works independently with general supervision on larger, moderately complex projects/assignments. In addition, the candidate sets objectives for their job area to meet the objectives of projects and assignments. | 07/17/2024 |
| 2748 | Neuralink Austin, TX Associate Chemist Bachelor OR M.S. of Science in Chemistry, Biochemistry, or a related field Exp: 1-2 years |
The Associate Chemist role will work with teams across the Neuralink organization to analyze the chemical and biological characteristics of manufacturing processes and finished devices. This will include various levels of product testing during R&D and release to obtain data that may be required for product approvals. Additionally, this data may be used to confirm patient safety of our products by applicable global regulations, regulatory guidelines, or voluntary consensus standards. Daily responsibilities may involve drafting internal procedures and test protocols, sample preparation, laboratory testing, method development, inventory management, and other miscellaneous laboratory tasks. The primary goal will be to assist in medical device chemical and biological characterization to support patient safety and regulatory approval. | 07/17/2024 |
| 2749 | Revvity San Diego, CA Biochemist I - Proteogenomics Bachelor’s degree in Physical Sciences, Life Sciences, or other related fields Exp: 1+ years |
BioLegend (a division of Revvity, Inc.) has an opening for a self-motivated individual with production experience in a fast moving and dynamic environment to join our Proteogenomics team! The biotechnician will be an integral member of a team, that manufactures and provides high-plex oligonucleotide conjugated antibodies panels to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform column chromatography manually and via automation, troubleshooting of problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 07/18/2024 |
| 2750 | Revvity San Diego, CA Research Associate I - Immunoassay (LEGENDplex BS in a Biology, Chemistry or other related field Exp: 1+ years |
This position is responsible for supporting immunoassay products development and manufacturing in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working with an experienced scientist on testing new hybridoma clones, qualifying the raw materials used for immunoassay products manufacturing and new immunoassay product development and launching. These immunoassay products may allow simultaneously detection of up to 13 important biomarkers for inflammatory diseases, stem cells, cancer, cardiovascular disease or neuron degenerative diseases, and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experiences in growing business in a fast-pace biotech industrial environment. He or she will be able to manage the assigned function and tasks with great communication skills in a timely manner with independence after appropriate training. | 07/18/2024 |
| 2751 | Revvity San Diego, CA Research Associate II - Immunoassay (LEGENDplex) BS in a Biology, Chemistry, or other related field Exp: 1+ years |
This position is responsible for supporting immunoassay product development and manufacturing in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working with an experienced scientist on testing new hybridoma clones, qualifying the raw materials used for immunoassay products manufacturing and new immunoassay product development and launching. These immunoassay products may allow simultaneous detection of up to 13 important biomarkers for inflammatory diseases, stem cells, cancer, cardiovascular disease, or neuron degenerative diseases, and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experience in growing business in a fast-paced biotech industrial environment. He or she will be able to manage the assigned function and tasks with great communication skills in a timely manner with independence after appropriate training. | 07/18/2024 |
| 2752 | Revvity San Diego, CA Biochemist I - GMP Beads Conjugation BS degree in chemistry/biochemistry, material science or life science. Exp: 0-1 years |
This biochemist role will be an integral member of our GMP team that develops and manufactures BioLegend’s regulated magnetic beads and antibody reagents produced in our US FDA registered cGMP manufacturing facility. This position will report to a GMP MOJO Scientist. The desired candidate must be a team-player who is organized and is able to work in a fast-paced environment to meet deadlines. Great attention to detail is also a skill that will allow the candidate to be successful. | 07/18/2024 |
| 2753 | Revvity San Diego, CA Research Associate I - Molecular Cloning Bachelors of Science in Biological Sciences Exp: 1+ years |
This position is responsible for developing recombinant protein/antibody research products in the Molecular Cellular Biology group. The research associate will be involved in the early stage of product development for recombinant protein/antibody products. The duties include preparing cell culture media, DNA purification, PCR and molecular cloning, bacterial and mammalian cell cultures, and purifying recombinant proteins/antibodies with several affinity tags, and weekly presentations of results to internal and external groups. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 07/18/2024 |
| 2754 | Revvity San Diego, CA Quality Control Associate I Bachelor’s degree in a scientific discipline Exp: 1+ years |
At BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team. | 07/18/2024 |
| 2755 | Revvity Boston, MA Associate Chemist B.S. degree in Chemistry, Biochemistry, Chemical Engineering Exp: 0-2 years |
We are seeking an Associate Chemist to join our team of scientists in the Research Reagents group manufacturing synthetic chemical products used throughout the world in scientific research applications. The Associate Chemist will also have an opportunity to work on the Microfluidics product line. This position will function as a member of the production staff and will participate in the transfer, implementation and on-going production of products in the laboratory. This is an on-site role based at our Boston South End manufacturing site. | 07/18/2024 |
| 2756 | Neurona Therapeutics South SF, CA Research Associate, Process Sciences Bachelor’s or master’s degree in chemistry, biology or biochemistry. Exp: 0-5 years |
Our ideal candidate is a self-motivated individual who has a passion for method development and qualification that can thrive in a fast-paced dynamic environment. The successful candidate will work as a member of the Process Sciences department and will be responsible for projects requiring design and qualification of process equipment. In addition, the candidate will interface with Manufacturing, Process Science, Facilities, Validation, QA, and Contract Engineering/vendor firms to produce detailed designs for procurement, construction, installation, start-up, and validation of process systems including systems for shipping product to clinical sites. This is a fantastic opportunity to join a small team, work on transformative science, and take part in building an exciting, science-driven company. | 07/18/2024 |
| 2757 | Q2 Solutions Marietta, GA Associate Scientist, Flow Cytometry Bachelor’s Degree in a scientific field including chemistry, biology or medical laboratory technology. Exp: 6+ months |
In this vital role, you'll support daily laboratory functions, including inventory management, pre-analytical sample handling, and more, ensuring efficient and effective operations. What you’ll be doing: Performing and documenting analytical procedures, adhering to SOPs and regulatory guidelines, and upholding our laboratory's high-quality standards. Analyzing routine data, identifying deviations or unusual results, and reporting these findings promptly to senior lab personnel to safeguard our scientific work's integrity. Engaging in quality investigations, preparing necessary materials for analyses, and demonstrating your commitment to scientific accuracy and rigor. Mentoring entry-level staff, facilitating their onboarding, and participating in continuous education initiatives to strengthen our team's expertise foundation. Taking part in cross-functional projects, communicating effectively across various teams, and advocating for safety, quality, and adherence to organizational standards and initiatives. | 07/18/2024 |
| 2758 | Q2 Solutions Indianapolis, IN Associate Scientist, Biotransformation Bachelor’s degree in a relevant scientific discipline Exp: 6+ months |
We are seeking an Associate Scientist, Biotransformation to join Q2 Solutions, IQVIA’s laboratory business in Indianapolis, Indiana. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. What You’ll Be Doing: Perform routine analysis and laboratory testing procedures to obtain data from pre-clinical and/or clinical specimens. Document analytical procedures in accordance with methods and regulatory guidelines. Assess whether analytical procedures are proceeding according to expectations and ensure results are within acceptable tolerances. Identify abnormal progress, potential quality failures, or unusual results and escalate to senior lab personnel. Prepare data analysis results for upload to LIMS system under the guidance of senior-level staff. Assist in writing laboratory procedures and techniques. | 07/18/2024 |
| 2759 | Q2 Solutions Durham, NC Associate Scientist Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology. Exp: 6+ months |
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Associate Scientist will be instrumental in conducting and documenting analytical procedures, ensuring compliance with SOPs and regulatory guidelines, and contributing to the advancement of our laboratory operations. | 07/18/2024 |
| 2760 | Q2 Solutions Marietta, GA Laboratory Assistant, Inventory Control Bachelor’s Degree or equivalent combination of education Exp: 6+ months |
As a Laboratory Assistant, Inventory Control you will be providing lab support, necessary to assist the local inventory process. You will also be managing reagent inventory for the Flow and PBMC departments. | 07/18/2024 |
| 2761 | NJ Bio Princeton, NJ QC Scientist (I&II) BS, MS, or PhD degree in chemistry, biology, biochemistry, or related discipline Exp: 1+ years |
The primary role is to provide analytical support for GMP manufacturing and process development. The QC scientist will develop, qualify, and execute analytical test methods for raw materials, highly potent APIs, antibody-drug conjugates (ADCs), and other pharmaceutical products in a GMP setting. | 07/18/2024 |
| 2762 | Avecia Cincinnati, OH Associate Chemist BS degree in Chemistry or related areas Exp: 0+ years |
As an Associate Chemist, you will execute chemistry and related activities for manufacturing, packaging and shipping of OliGrow oligonucleotides according to company processes. | 07/18/2024 |
| 2763 | Noah Medical Sunnyvale, CA Clinical Engineer Bachelor’s degree in Engineering or Science; Master’s degree preferred Exp: 0-5 years |
The Clinical Engineering Team at Noah Medical is dedicated to ensuring the products Noah is developing meet all of the clinical and user needs. We collaborate closely with our end users (physicians) to understand their needs and the clinical value Noah’s products will bring them. The Clinical Engineering team also works closely with cross-functional development teams to represent clinical value propositions for patients and providers throughout the design and development of new products. Join us to contribute to Noah Medical's growth and to shape the future of medical robotics. | 07/18/2024 |
| 2764 | Noble Life Sciences Sykesville, MD Research Technician Bachelor’s degree in biological sciences, biomedical engineering, or a related field. Exp: 1+ years |
Job Description: Compliance: Perform assigned tasks and responsibilities under the direction of the Scientist(s) and/or the Study Director(s) and in accordance with relevant study protocols, regulations, and Standard Operating Procedures (SOPs); Training: Ensure personal training is documented according to Noble SOPs prior to the performance of associated procedures; Procedure Preparation: Label tubes and other supplies needed for collecting and processing specimens. Prepare reagents needed for collection or processing of specimens. Performance of Procedures: Process various blood and tissue samples. Maintain quality, safety, and/or infection control standards. Perform procedures using various instrumentation according to Noble SOPs; Documentation: Maintain lab notebooks and document experimental procedures and associated data. Assist in writing deviations and preparing responses to quality assurance audits related to duties performed. Laboratory Maintenance: Take ownership of assigned laboratories. | 07/18/2024 |
| 2765 | NorthStar Beloit, WI Radiopharmaceutical Manufacturing Associate Associate’s or Bachelor’s degree in a STEM discipline Exp: 0-1 years |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. | 07/18/2024 |
| 2766 | NorthStar Beloit, WI Quality Control Analyst/Senior Quality Control Analyst Bachelor’s Degree in Chemistry, Biology, or other related scientific discipline Exp: 1+ years |
The primary role of this position is to conduct and validate various biological and analytical quality control assays associated with the processing of radiopharmaceutical isotopes and drugs to ensure compliance with established standards. This role requires extensive training on radiation safety including ALARA (“as low as reasonably achievable”) principles. Duties will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. | 07/18/2024 |
| 2767 | Machine Solutions Flag Staff, AZ Medical Device Testing Technician Bachelor’s level degree, preference for engineering or technical experience or Exp: 0+ years |
Machine Solutions testing equipment is used to evaluate and quantify the performance of our customers’ interventional devices such as stents, catheters, and guide wires. Testing/applications technicians are responsible for lab-based tasks, which include sample processing, contract testing, measuring, recording, analyzing results and generating reports on MSI equipment with in-house or customer product. The technician will learn how to operate Machine Solutions equipment and use this knowledge to host customer training and perform quality inspections to ensure equipment meets operational specifications. An ideal candidate will be someone who enjoys working with their hands and enjoys the challenge of finding unique solutions to meet our customer’s needs. | 07/01/2024 |
| 2768 | Macrogenics Rockville, MD Manufacturing Associate II - Cell Culture Bachelor’s degree in a related discipline and a minimum of three years of related biopharmaceutical manufacturing experience in FDA regulated, control Exp: 1+ years |
The Manufacturing Associate II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Protein Purification area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 07/01/2024 |
| 2769 | Macrogenics Rockville, MD Manufacturing Associate I - Cell Culture Bachelor’s degree in a related discipline Exp: No Experience |
The Manufacturing Associate I participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 07/01/2024 |
| 2770 | MagBio Genomics Gaithersburg, MD Production and Fulfilment Associate Bachelor's Degree in Biology or equivalent science-related field; or equivalent combination of education and experience. Exp: 0-2+ years |
This position is responsible for the timely and efficient scheduling production, packaging and shipping of standard and custom products, and for providing support to other areas of manufacturing to ensure timely product delivery. Responsibilities with reagent production, shipping, and order fulfilment. | 07/01/2024 |
| 2771 | Magnolia Medical Technologies Seattle, WA Engineering Intern, Product Development (Hybrid) Pursuing an engineering degree, or related BA/BS degree, or pursuing a related MA/MS. Exp: Entry Level |
The Engineering Intern performs, under direct supervision, and contributes to the Engineering and Product Development Department of Magnolia Medical Technologies, Inc. The Intern is exposed to the medical device industry and Magnolia Medical's company culture through partnering with the organization’s teams, department supervisors and leaders who provide informal mentoring and coaching towards success. The Engineering Intern develops working knowledge of product development, works in a changing environment, and will further develop skills utilized industry wide in regulatory environments. | 07/01/2024 |
| 2772 | Mallinckrodt Pharmaceuticals St. Louis , MO Chemical Process Technician Minimum of a Bachelor's degree in Chemistry, Biology or other science degree. Exp: 1-3+ years |
Develop and produce pharmaceutical products via multiple methodologies, follow standard operating procedures, maintain compliance with Good Manufacturing Practices. | 07/01/2024 |
| 2773 | Mallinckrodt Pharmaceuticals Hobart, NY Quality Technician I - First Shift Bachelor Degree in science related field (Chemistry, Biology) is preferred Exp: I: Class/previous work exp in science related field II: Working knowledge of chemistry required III: Min 1-3 years of exp in cGMP facility |
Perform basic wet chemistry, preparation of reagents/solutions, and sample reconciliation following approved methods. | 07/01/2024 |
| 2774 | Mallinckrodt Pharmaceuticals Hobart, NY Validation Technician III Bachelor Degree in engineering discipline, life sciences or technical field related to pharmaceutical manufacturing is preferred Exp: 0-1 years |
Assists with multiple cross-functional projects from development through release for commercial implementation. Supports departmental priorities and senior level engineers with guidance from the department manager. May support the execution of validation studies as needed, including assisting in pre-run training, product sampling, and review of documentation for completeness and alignment with good documentation practices. Assists in the analysis and review of data generated by validation studies performed within the department. | 07/01/2024 |
| 2775 | Mallinckrodt Pharmaceuticals Hobart, NY Validation Engineer I Bachelor Degree in engineering discipline, life sciences or technical field related to pharmaceutical manufacturing is preferred Exp: 1-2 years |
Assists with multiple cross-functional projects from development through release to production. Projects include new facilities startup, manufacturing equipment and packaging line FATs and qualifications. Independently executes activities in support of the Validation Department priorities with minimal guidance from the department manager. Provides technical assistance during investigations of equipment/process/product issues. Supports validation deviations related to equipment/process/product. Execute validations as needed, including assisting in product sampling, auditing and technical review functions as defined in study protocols. Analyzes data, utilizing appropriate statistical methods, generated by validation studies performed by the Validation group to determine process capabilities. | 07/01/2024 |
| 2776 | Mallinckrodt Pharmaceuticals Madison, WI Quality Analyst Bachelor’s Degree Exp: 1+ years |
The Quality Analyst ensures that all materials, activities, processes, and specified conditions involved in daily device manufacturing, processing, and packaging meet current GMP standards and comply with relevant procedures and standards to maintain product quality integrity. Additionally, the Quality Analyst manages nonconforming material reports, plans material review board meetings, and oversees the status of quarantined and scrapped materials. | 07/01/2024 |
| 2777 | Mammoth Biosciences Mammoth Brisbane, CA Research Associate II/Senior Research Associate – LNP Formulation Bachelor's degree in chemistry, pharmaceutical sciences, bioengineering, chemical engineering, or related discipline with 1+ years of experience or Ma Exp: 0-1 years |
In this role, the successful candidate will be contributing to the formulation efforts of Mammoth’s proprietary CRISPR nuclease systems, supporting the formulation and physiochemical characterization of the candidates for a variety of therapeutic indications. In addition, this candidate will be contributing to the analytical method development to support the formulation discovery and production of test articles to support Mammoth’s ex-vivo and in vivo studies. | 07/01/2024 |
| 2778 | Mariana Oncology Watertown, MA GMP Manufacturing Technician Bachelor’s Degree, Associate Degree, or 5 years of experience working in a GMP manufacturing environment in the pharmaceutical or biotechnology indust Exp: 0-5 years |
Mariana Oncology is focused on an extremely exciting field of oncology of precision radiopharmaceuticals to treat unmet need in solid tumors. We are at the vanguard in developing best in class alpha and beta emitting radio ligands targeting cancer tumors while mitigating destruction to healthy tissue and cells. We have built a fully integrated, leading radiopharmaceutical platform, that is bringing together novel target biology insights, innovative multimodal ligand discovery, and enabling translational infrastructure. We are seeking an experienced GMP Manufacturing Technician to join Mariana’s Manufacturing organization, advancing personalized medicine and radiopharmaceuticals. | 07/01/2024 |
| 2779 | Mariana Oncology Watertown, MA Quality Control Analyst I/II Master’s degree in biochemistry, chemistry or related discipline with 0-2 years exp, or Bachelor's degree with 2-4 years exp Exp: 0-2 years |
We are seeking an experienced Quality Control Analyst I/II to join Mariana’s Clinical Manufacturing organization, advancing personalized medicine and radiopharmaceuticals. You will be responsible for supporting the release and stability testing of our clinical therapies produced in our GMP manufacturing suite in Watertown. This person will play a role in creating and maintaining the highest standard of excellence for our therapies to treat cancer patients. | 07/01/2024 |
| 2780 | Marvel Biome Woburn, MA Research Associate BS or MS in Molecular Biology, Microbiology, or Cell Biology required Exp: 0-2 years |
We are seeking a full-time Research Associate to join a highly collaborative team using the latest molecular biology, protein biochemistry, and -omics analysis techniques to develop microbiome-based therapies. In addition, there will be opportunities to assist in the execution of pre-clinical studies to evaluate treatment efficacy. The ideal candidate is obsessed with the question of how to best design and execute experiments to identify treatment-improving therapies. This is a unique opportunity to work at a nimble, forward-thinking microbiome start-up and help build the foundation for microbiome as therapeutics. | 07/01/2024 |
| 2781 | MatTek Ashland, MA Production Associate I Bachelor’s degree in biology or equivalent with no previous work experience Exp: 0+ years |
Participates in duties associated with manufacturing of MatTek tissue models according to SOPs where applicable. May also perform duties assigned under Laboratory Assistant, as needed. | 07/01/2024 |
| 2782 | Maze Therapeutics San Francisco, CA Research Associate, In Vivo Pharmacology Bachelors degree in biology, pharmacology, or other relevant field is required Exp: 1+ years |
Are you driven by a passion for scientific discovery and a desire to make a tangible impact on human health? We're seeking a passionate, creative, and dedicated Research Associate to join our in vivo pharmacology team. In this role, you will be pivotal in conducting pharmacokinetic studies that drive our research projects forward, while also contributing to preclinical pharmacodynamic and disease models. Under the guidance of the Director of Pharmacology, your work will directly support the discovery of new drug candidates and advance our understanding of disease mechanisms. Additionally, as a rapidly growing biotech company, we offer an exciting and collaborative work environment where every team member plays a vital role in our success. | 07/01/2024 |
| 2783 | Mdxhealth Irvine, CA Product Development Associate Bachelor's degree with 1-2 years of experience working in research & development or Master's degree with 0 to 3 years’ experience. Exp: 0-3 years |
The Product Development Associate is involved in assisting with the planning, conducting, and analyzing experiments leading to validation of diagnostic tests in the field of oncology. The PD Associate works in a team and needs to communicate relevant information to professional colleagues and to participate constructively in discussions that will impact the performance of the final product. | 07/01/2024 |
| 2784 | Mdxhealth Irvine, CA Inventory Control Associate High School Diploma or Bachelor's Degree Exp: 1-2+ years |
The function of an Inventory Control Associate is to keep track of the goods and supplies of the Operations teams, both incoming receipt and outgoing release to the laboratories. The Inventory Control Associate is to keep records of inventory counts, generate and place purchase orders, coordinate with vendors, maintain inventory of items in stock, and perform data entry of this information. The Inventory Control Associate is to monitor and handle purchases to ensure arrival in a timely fashion in the quantity and quality that upholds mdxhealth standards while maintaining supplier and interdepartmental relationships. | 07/01/2024 |
| 2785 | MedAbome Fremont, CA Research Associate (Molecular Biology) M.S. or B.S. degree in life science with academic or industrial experience in biological research Exp: 0+ years |
Perform molecular biology experiments to support drug discovery and development; Participate in antibody engineering, cell line generation, in vitro and in vivo assays. | 07/01/2024 |
| 2786 | MedAbome Fremont, CA Research Associate (Cell Biology) M.S. or B.S. degree in life science with academic or industrial experience in biological research Exp: 0+ years |
Maintain cell lines and perform cell-based assays to support antibody drug discovery; Participate in antibody generation and characterization, such as fusion, ELISA, FACS and other cell-based assays; Participate in small animal studies. | 07/02/2024 |
| 2787 | Medmix Flowery Branch, GA Technical Project Engineer Bachelor’s degree in mechanical or industrial engineering Exp: 1+ years |
We are looking for a Technical Project Engineer to join us at medmix. This exciting opportunity will allow you use your skills to identify areas of improvement and propose recommendations to management. You will lead and drive the implementation of your recommendations and assess its impact to the business. If you are eager to learn, strive for personal development, are highly motivated and organized, and a great communicator, you can help us drive medmix to the next level. As a Technical Project Engineer you will help us to take effective project management to the next level. Responsibilities: Realization of injection molding life cycle projects in the segments industry, dental and surgery, Lead interdisciplinary project teams, Create and update of project plans and necessary documents, Reach the goals set for cost, time and quality, Delegate and control tasks and execution of work packages within the projects, Execution of mile stone meetings | 07/02/2024 |
| 2788 | Medpace Cincinnati, OH Laboratory Technologist - Sample Processing Bachelor's degree in a Biological Science field or Chemical Science field Exp: 1+ years |
Our biorepository activities are growing rapidly, and we are looking to add to our sample processing team! The Laboratory Technologist will aid in the development and growth of the biorepository sample processing department. The ideal candidate will have strong critical thinking and problem solving abilities. This position will be a full-time, position in Cincinnati, OH. | 07/02/2024 |
| 2789 | Medpace Irving, TX Clinical Research Associate (CRA) Must have a minimum of a Bachelor’s degree in a health or science related field Exp: 0+ years |
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health/life science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you! | 07/02/2024 |
| 2790 | Medpace Cincinnati, OH Chemistry Laboratory Technician A minimum of a Bachelor's degree, with previous experience in a research laboratory Exp: 1+ years |
Responsibilities: Prepare samples according to project protocol and/or related SOPs; Maintain compliant laboratory documentation; Perform data analysis and data checking; Interpret results obtained for accuracy and acceptability; Clean and sterilize laboratory equipment; and Other duties deemed necessary. | 07/02/2024 |
| 2791 | Medpace Cincinnati, OH Laboratory Quality Assurance (QA) Auditor Bachelor’s degree in the science or a related field Exp: 1-3 years |
The QA Auditor role will be responsible for both internal and external audits, as well as coordinating, conducting, and tracking company-wide Regulatory Training, CAPA Investigations and Metric Analysis. This role will also ensure Compliance to Standard Operating Procedures (SOPs), current Regulations, and Standards. In addition, the Auditor will assist in the creation and maintenance of Controlled Documents. This role is highly visible to Medpace Internal and External Clients; therefore, this role requires excellent Communication Skills, a Proactive Enthusiasm, and Critical Thinking. | 07/02/2024 |
| 2792 | Medpace Cincinnati, OH Laboratory Technologist Bachelor's degree in a Biological Science field or Chemical Science field Exp: 0+ years |
The Laboratory Technologist at Medpace Reference Laboratories plays a pivotal role in research based drug development within the pharmaceutical industry. Due to our recent growth, we are in need of qualified and focused driven individuals, like yourself! You would have the unique opportunity to work on the laboratory side of the fast paced medical world by conducting routine and esoteric testing on blood, tissue, and body fluids. If you have an analytical mind set, and enjoy working in a team-oriented laboratory setting, this could be the opportunity for you! | 07/02/2024 |
| 2793 | MedPharm Durham, NC Associate Scientist-Performance Testing Bachelors degree, education may be used in lieu of experience Exp: 0-2 years |
The Associate Scientist is an essential member of the laboratory team. They work with the Performance Testing team to conduct in vitro permeation and release testing for topical and transdermal formulations. They also conduct analysis of research projects and results and help develop nonstandard tests. Associate Scientists have the opportunity to collaborate with fellow scientists in study planning, formulation development, analytical, and tissue culture. We are looking for an eager individual who wants to develop personally and professionally. You should have a strong attention to detail, be a go-getter, and be continuously striving for self-improvement. You are passionate about good science and want to help out in any way possible. We are looking to invest in someone who wants to grow not only in this role but also in their scientific career. | 07/02/2024 |
| 2794 | Medtronic Fridley, MN Hardware Engineer I Bachelors degree in Electrical Engineering, Computer Engineering or related field required Exp: No Experience |
This position will provide Electrical Design and System Test support for the Translational Research System team on Neuromodulation & Pelvic Health Implantable products such as cutting-edge neurostimulator systems for Deep Brain Stimulation, Spinal Cord Stimulation, and Sacral Nerve Modulation. The individual will support all phases of development including definition, design, troubleshooting, characterization, and verification of medical device research systems. The individual will be an integral part of the R&T organization delivering the highest quality, life changing technology to our patients. This role requires a strong background in hardware development and testing, system integration and testing, and a passion for improving healthcare through technology. | 07/02/2024 |
| 2795 | Medtronic Danvers, MA Process Engineer I Bachelors Degree in a related engineering discipline (i.e., mechanical, biomedical, industrial, materials science) Exp: No Experience |
As a Process Engineer I, you will be involved with process development, setting up manufacturing operations, and interfacing cross-functionally with other key engineering expertise to develop a product. In this role, you will part of a team but will be able to work independently to determine and develop approaches to solutions. You will communicate with internal and external customers and suppliers. Your work will involve collaboration and dynamic interactions with R&D and Design Assurance regarding products in the development pipeline and with operation team members for new or iterative product implementation. | 07/02/2024 |
| 2796 | Medtronic North Haven, CT Manufacturing Engineer I Bachelors degree, preferred in Engineer Exp: No Experience |
The Manufacturing Engineer will be working with highly motivated team members and dynamic work environment. This is a great opportunity to interact and work with broad cross-functional groups including different manufacturing sites engineering, quality, share-services, marketing team and extensive business platforms, and suppliers to continuously improve the manufacturability. | 07/02/2024 |
| 2797 | Meissner Camarillo, CA Quality Assurance Coordinator Bachelor’s Degree from a 4-year accredited college or university Exp: 1-3 years |
As part of the Quality Assurance team, you will work closely with Quality Control, Customers, Engineering, Manufacturing, Sales and Marketing teams to ensure that solutions in development and in production meet the needs of our customer base and are compatible with the regulatory environment of our industry. As part of the Quality Assurance team, you will work closely with Quality Control, Customers, Engineering, Manufacturing, Sales and Marketing teams to develop and improve our Quality Management System (QMS). Work collaboratively with the team to develop, implement, maintain and ensure the performance of the company’s QMS. Utilizing leading-edge technology, you will support customer inquiries by monitoring Meissner’s Quality inbox, coordinating responses and assigning inquiries to the appropriate parties. Support and ensure compliance with established company policies and procedures, objectives, quality assurance program. Support implementation of QA procedures and documents. Review SOPs to ensure alignment with quality guidelines and documents. | 07/02/2024 |
| 2798 | Meissner Camarillo, CA R&D Scientist I Bachelor’s degree required in STEM-related field Exp: 1-5 years |
Are you a passionate scientist ready to push the boundaries of research and development? Join our dynamic R&D team as an R&D Scientist I, where you’ll spearhead groundbreaking experiments, analyze cutting-edge data, and contribute to revolutionary product advancements. If you thrive in a collaborative environment and are driven by discovery, we want you on our team! Our customers use our products and technologies to develop new therapeutics and many familiar products that support our modern lifestyle. At the core of these products, are in-house technologies that are developed and maintained by highly talented and self-driven engineers and scientists. Participate in technology development projects, Assist in technology transfer of R&D Activities to manufacturing, Support our technologies to continuously improve our products and processes. | 07/02/2024 |
| 2799 | Teva Pharmaceuticals Salt Lake City, UT Quality Control Analyst I Bachelor’s degree, preferably in the sciences or any combination of equivalent education Exp: 0+ years |
Teva has an opportunity for a passionate Chemist to join our team. As a key part of our dedicated, friendly, and collaborative Product Quality Team, you’ll play an essential role in laboratory testing of pharmaceutical product in support of commercial product release. This role is great role to learn the pharmaceutical manufacturing process. Many of our entry level lab analysts advance into other roles in Science, Quality and Production. | 07/02/2024 |
| 2800 | Mercury Bio Santa Fe, NM Research Associate BS or MSc in related fields and previous research experience Exp: 1+ years |
Mercury Bio has immediate openings for Research Associates with expertise in molecular genetics, biochemistry, bioinformatics, immunology and microbial or human cell culture. Ideal candidates should have a BS or MSc in related fields and previous research experience. This position requires creative and critical thinking, as well as the ability to work independently. Mercury Bio is located in Santa Fe, NM and focuses on the development of RNA therapeutics to control gene expression in humans in a safe and dose-dependent manner. | 07/02/2024 |
| 2801 | Meridian Bioscience Memphis, TN Quality Assurance Associate Bachelor’s degree from accredited institution in life science, chemistry, pharmaceutical science, statistics, or health/human services related field. Exp: 0-5 years |
The Quality Assurance (QA) Associate will support QA processes, programs, and conduct QA activities. This position will uphold standards, methods, and procedures for all stages of production. This position will identify continuous process improvement areas, in compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GLP) processes and documentation for quality control activities. This requires excellent technical skills and abilities, analytical and mathematical skills, organizational and time-management skills, verbal, and written communication skills, plus ability to apply attention to detail. | 07/02/2024 |
| 2802 | Meridian Bioscience Memphis, TN Quality Control Analyst Bachelor's degree in a scientific discipline or equivalent Exp: 1 years |
The Quality Control Analyst position performs testing and inspection of raw materials, in-process and finished products, and audits the corresponding documentation in compliance with internal SOPs and applicable regulatory requirements, participates in test method validation development and execution, and assists in the training and development of new Quality Control Analysts. The Quality Control Analyst is also responsible for performing duties required in the application and continued improvement of the company’s Quality System. | 07/02/2024 |
| 2803 | Meridian Bioscience North Billerica, MA Research Associate Bachelor of Science degree required, experience with analytical chemistry strongly preferred Exp: 0+ years |
Primary role is to run experiments, acquire and record data.Tasks/Duties/Responsibilities: Support projects by conducting experiments, acquiring, and accurately documenting data. Contribute to completion of milestones associated with specific projects. Expected to grow and develop in this role and be able to draw conclusion from studies and design experiments. | 07/02/2024 |
| 2804 | Meridian Bioscience Memphis, TN Lab Production Associate (Antigens and Cell Culture) Bachelor’s or Master’s degree from an accredited institution with a relevant scientific discipline such as Chemistry, Biology, Biochemistry, Molecular Exp: 0+ years |
The Lab Production Associate position is responsible for performing assigned manufacturing and laboratory support activities according to company policies, SOPs, and quality regulations. The position will be responsible for performing upstream and downstream bioprocessing procedures to support the commercial manufacturing of native antigens, recombinant proteins, antibodies, and blockers. Upstream processes include tissue culture, cell bioreactors, fermentation, virus propagation, cell and virus bank production, and buffer/media preparation. Downstream unit operations include harvest, clarification, chromatography, centrifugation, TFF (UF/DF), filtration, formulation, and fill-finish. The candidate will be required to maintain an assigned lab area and perform equipment and lab cleaning procedures. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO1345 regulations. | 07/02/2024 |
| 2805 | Merit Medical South Jordan, UT Mfg Engineer I Bachelor’s or Master's Degree in Engineering Exp: 0+ years |
Performs routine technical work such as the design, manufacture and operation of structures, machines and systems under general supervision and guidelines. Performs routine technical work requiring the application of standard techniques, procedures, and criteria in carrying out engineering tasks. Uses limited amounts of discretionary judgment in making decisions regarding technical alternatives. Performs work of some higher technical level for training purposes, and work is screened to ensure correct application of scientific principles. Works on special projects, writes ECN's, and may create prototypes under general direction. Performs other related duties and tasks as required. | 07/02/2024 |
| 2806 | Merit Medical South Jordan, UT R&D Engineer II - (Endovascular) Part-time Bachelor’s Degree in Engineering or technical field related to the department of assignment Exp: 0+ years |
Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision and guidelines. This position is 20 hours a week in the RND Endovasular division of Merit Medical. | 07/02/2024 |
| 2807 | Merit Medical South Jordan, UT Engineer II (Annual) Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision Exp: 0+ years |
Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision and guidelines. | 07/02/2024 |
| 2808 | Merit Medical South Jordan, UT Technician III Bachelor's Degree with 1 year of exp, Associate's Degree with 3 years of 3 years tech exp, or High school Diploma with 5 years of tech exp Exp: 1+ years |
Performs non-routine technical assignments of substantial variety and complexity. Performs assignments and may assist in planning assignments of a non-routine nature for which operational precedents are not fully applicable. Prepares test specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Extracts engineering or other data from various reports, processes the data, and presents the data. Receives technical advice from engineers or supervisor for complex problems. Working overtime may be required for this position. Performs other duties and tasks as required. | 07/02/2024 |
| 2809 | Meso Scale Diagnostics Gaithersburg, MD Scientist I, Bioanalytical Lab Bachelor's degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, or other related area is req Exp: 1+ years |
The Bioanalytical Scientist I provides supervision of daily laboratory operations, offers guidance, leadership and direction to lab personnel to ensure on-time completion of customer projects. This includes leading initiatives for the transfer of newly developed assays that have been developed for customers to the company's Bioanalytical Lab, supporting new instrumentation intended for use in sample testing services and managing studies performed in accordance with relevant regulations. This position will directly supervise the work of others in their group and/or across interdisciplinary teams. The Bioanalytical Scientist I will lead and/or direct the work of others, to include establishing the scope of work assignments, experiments and work schedules/deadlines. They are expected to independently manage multiple projects yielding high quality results, and provide oversight and guidance to other team members as needed. | 07/02/2024 |
| 2810 | Meso Scale Diagnostics Rockville, MD Quality Control Analyst I Bachelor’s degree in relevant field preferred. Associate’s degree in relevant field required. Exp: 0+ years |
Under general supervision, the Quality Analyst I performs routine quality control inspection, testing and data analysis for various incoming, in-process, and final products within MSD’s protein-based immunoassay catalog. This position will execute various laboratory cleaning activities to help support overall operations of Quality/Product Control. | 07/02/2024 |
| 2811 | Meso Scale Diagnostics Gaithersburg, MD Bioanalytical Associate I Bachelor’s degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, or other related area is req Exp: 0-2 years |
A Bioanalytical Associate I is responsible for handling biological samples, reagents, and materials in support of sample testing and assay service projects. This is a laboratory based position whose primary function will be sample management and handling, under direct supervision and direction. The incumbent may also perform protein-based immunoassays on a routine basis with relatively high throughput (2-8 plates per day). The incumbent is expected to adhere to all standard operating procedures and policies established for execution of Bioanalytical studies and sample testing projects under applicable regulatory compliance requirements. | 07/02/2024 |
| 2812 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Mechanical Bachelor’s degree in Mechanical Engineering Exp: 0+ years |
The Mechanical Engineer I is responsible for mechanical design, testing, and documentation of new instrumentation and support of exisiting instrumentation for the biodefense, clinical and life-science markets. Design work will include the design of precision mechanisms and complex assemblies that include machined, molded and sheet-metal components. | 07/02/2024 |
| 2813 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Automation Bachelor’s degree in Computer Science or Electrical, Mechanical, or Systems Engineering is required Exp: 0-1+ years |
The Automation Engineer I will design and build high performance, automated process equipment used for manufacturing and/or laboratory automation systems. These systems include, but are not limited to automated reagent dispensers, assembly, machine vision, and liquid handling systems for micro-plate test kit and micro-fluidic assay cartridges used in the biodefense, clinical, and life-science markets. | 07/02/2024 |
| 2814 | Meso Scale Diagnostics Rockville, MD Production Control Technician I Bachelor’s degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, engineering or a related fie Exp: 0-1+ years |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. | 07/02/2024 |
| 2815 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Systems Bachelor’s degree in Systems, Mechanical, or Electrical Engineering or a closely related field Exp: 0-1+ years |
The Systems Engineer I is responsible for assisting in the development and management of requirements and specifications, system integration and testing of electromechanical, fluidic, thermal control, and imaging systems, and formal verification and validation testing. | 07/02/2024 |
| 2816 | MethodSense Morrisville, NC Quality and Safety Engineer Bachelor’s degree in biomedical engineering or alternative engineering degree. Exp: 1-7 years |
We are looking for talented Quality and Safety Engineers to join our experienced team. If you can commit yourself to supporting a passionate regulatory affairs and quality assurance business dedicated to their clients, you can have a career with us. We need someone with honesty, integrity and excellent communication and interpersonal skills. The position requires the ability to work with client company executives, test labs and FDA regulators. It also requires agility and love for knowledge. If you want to join a high energy purposed team, please apply. | 07/02/2024 |
| 2817 | Metrohm Charlotte, NC Field Service Technician - Lab Equipment A degree or certification in Chemistry (or related STEM field) is preferred. Exp: 0+ years |
Field Service Technicians provide on-site preventative maintenance and basic service for Metrohm laboratory instruments. You will attend training classes at our headquarters in Tampa, FL. Field Service Technicians get to travel to a diverse group of labs, meet different people and see various instrument applications at work. You will have the resources to support the client face to face, via phone, email and Microsoft Teams. This is a remote position that requires some overnight travel in the NC/SC region. | 07/02/2024 |
| 2818 | MicroAire Surgical Instruments Charlottesville, VA Design Verification Engineer (Test Development) Bachelor’s in Mechanical or Biomedical Engineering required. Exp: 0+ years, internship exp applies |
Develops Plans for the Appropriate Verification and Validation (testing) of new products, line extensions, and product redesigns. | 07/02/2024 |
| 2819 | MicroVention Aliso Viejo, CA Engineer I, R&D Bachelor’s degree in Engineering or Scientific field. Exp: 6 months |
Support development of medical device products with work including writing or verifying specifications; designing new products and fixtures; testing processes and equipment; and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Job duties: Develop new product concepts and products. Provide engineering design and process development.Generate intellectual property; write invention disclosures. Supervise assemblers, technicians, and specialists. Partially self-directed and capable of meeting project goals with supervision. Some travel required. Perform additional responsibilities as assigned. | 07/02/2024 |
| 2820 | Mikart Inc Atlanta, GA Quality Control Analyst Bachelor of Science in Chemistry with 0 yrs exp or Bachelor of Science degree in a related science plus 1 year of applicable exp Exp: 0-1 years |
The Quality Control Analyst for Mikart, LLC is responsible for conducting analyses on various components, in process materials and finished dosage forms. Document all analyses performed through the use of notebooks and official forms. Immediately report any anomalies to the Team Leader. Enter data into spreadsheet templates and verify accuracy by performing minimal manual calculations. Assure the accuracy of all data used for batch calculations. Conduct all operations in strict accordance with applicable regulations, guidance documents, SOPs and Mikart policies and procedures, including computer data acquisition and integrity policies. Assure that all laboratory areas and workspaces are maintained in a neat and orderly fashion. Perform necessary cleaning, maintenance, and calibration of instrumentation, as required. Maintain or request appropriate supplies and materials necessary to complete all assignments. Assist in maintaining accurate documentation of all supplies and chemicals received and used. Maintain appropriate records of waste storage and disposal in accordance with Mikart procedures and appropriate regulations. Assure that laboratory reagents, solutions, standards, samples, and controlled substances are used and stored properly and in accordance with all applicable regulations and guidelines. Secure all assigned samples while testing is in progress. Assure all materials used in analyses are within their established expiry period. | 07/02/2024 |
| 2821 | Mikart Inc Atlanta, GA Quality Control Analyst (Microbiologist) Bachelor of Science in Biology with 0 yrs exp or B.S. degree in a related science plus one-year applicable experience, or other appropriate combinatio Exp: 0-1 years |
The Quality Control Analyst (Microbiologist) for Mikart, LLC is responsible performing analyses on incoming samples requiring microbiological testing. Receive incoming samples, including water, environmental, raw material and dosage form samples, and insure that information is accurately and promptly entered into logs. Perform microbiological or other testing required on incoming samples safely and in accordance with all GMP, USP and Mikart specifications and procedures. Document all analyses performed through the use of notebooks and official forms. Immediately report any anomalies to the supervisor. Report any discrepant, suspect or out-of-specification results to the Microbiology Supervisor immediately. Accurately follow investigation plan directives issued by supervisory personnel. Assure proper handling of materials under test, including controlled substances, and ensure proper storage of all samples. Assure that all waste is processed according to procedures before disposal. Complete usage and maintenance logs accurately and promptly for instruments and equipment present in the micro lab. Receive and assure that all laboratory reagents, solutions, standards, samples, and controlled substances are used, stored properly and in accordance with all regulations and guidelines. Secure all assigned samples while testing is in progress. Assure all materials used are within their established expiry period. Verify that all laboratory equipment is within the active calibration period. | 07/02/2024 |
| 2822 | Miltenyi Biotec Boston, MA Clinical Trial Associate Bachelor's Degree Exp: 0-2 years |
The Clinical Trial Associate (CTA) will support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. Collaborate with Clinical Trial Manager(s) to assist in the operational and logistical aspects of clinical trial management tasks (e.g. start-up, maintenance, and close-out activities) according to ICH-GCP and standard operating procedures. Liaise with CROs and other clinical vendors to ensure deliverables are met and communication is efficient. Partner with Investigators and clinical site staff to ensure optimal Sponsor-Site relationships. Assist in the management of study to ensure adherence to timelines and achievement of study goals while ensuring high quality. | 07/02/2024 |
| 2823 | Mission Bio South SF, CA Sr Bioinformatics Scientist, Remote Master's or PhD degree in Computational Biology, Bioinformatics Exp: Relevant grad/postdoc experience are also welcome |
We are seeking a talented and motivated Computational Biologist/Bioinformatics Specialist to join our team. This role will be pivotal in supporting our pharma accounts, driving product development and clinical traction by utilizing advanced data analysis techniques, algorithm development, and effective communication with customers. The ideal candidate will have a strong background in data analysis, with a focus on single-cell analysis, and possess the skills necessary to refine algorithms for production environments and ensure compliance with regulatory standards. | 07/02/2024 |
| 2824 | Moderna Norwood, MA Engineer I, Process Engineering Bachelor’s degree in chemical engineering, mechanical engineering, or related field. Exp: 0-2 years |
In this role, you will support the operability and reliability of GMP manufacturing process equipment at Moderna's manufacturing facility in Norwood, MA. This individual will assist Facilities and equipment End Users with routine troubleshooting and optimization of process equipment. Applicants should enjoy working in a fast-paced, dynamic, and innovative environment. | 07/02/2024 |
| 2825 | MP Biomedicals Solon, OH Production Chemist Bachelor of Science in Chemistry, Biochemistry, or Biology or equivalent work/school experience. Exp: 0-3 years |
The production chemist will be trained on two different product lines. This position will rotate training through two manufacturing areas that include Immunology and Molecular Biology Liquids. Learn and be responsible for a wide variety of product formulation tasks. Follow and optimize production processes while following safety protocols. Produce quality research products in a timely fashion to meet customer demand. Responsibilities will include: Operation of lab equipment including spectrophotometer, plate reader, centrifuges, pipettors, etc., Purification of antibodies from whole antisera using affinity chromatography methods. Conjugation of antibody to enzymes/fluorochromes. Maintenance of detailed records of products in production. Perform Quality Control testing for Immunology products (UV-VIS, Immunoelectrophoresis, and ELISA). | 07/02/2024 |
| 2826 | Myriad Genetics Salt Lake City, UT Research Associate (Onsite) BA/BS or MS in Molecular Biology, Cell Biology, Genetics, Biochemistry, Biophysics, Chemistry, or a related discipline Exp: 1+ years |
We are looking for a Research Associate to join our interdisciplinary R&D team that includes scientists in Salt Lake City and South San Francisco (this posting is for a role in Utah). The ideal candidate will have hands-on experience with a range of current molecular biology techniques, with particular focus on NGS. We are seeking a collegial teammate who is curious and rigorous, an individual who shares our enthusiasm for improving people’s lives by building the products that power precision medicine. | 07/02/2024 |
| 2827 | AlloyTx Waltham, MA Research Associate, Antibody Discovery B.S. in Immunology, Molecular Biology, or related discipline. Exp: 0-2 years |
As a Research Associate, Antibody Discovery, you will work with our ADS team to build new antibody technologies for the discovery of antibody-based therapeutics. You will be using the very latest single-cell techniques with the goal of identifying drug candidates in close collaboration with our partners. This role requires strong molecular biology skills, and the ability to plan and execute lab activities efficiently. This role will report to Head of In-Vivo Antibody Discovery with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This is you! | 5/17/2024 |
| 2828 | AlStem Bio Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 5/17/2024 |
| 2829 | Alta Sciences Columbia, MO Associate Scientist, DCA M.S. Exp: +1year |
In the performance of their respective tasks and duties, the Associate Scientist, Dose Concentration Analysis are expected to be engaged in the conduct of or responsible for the supervision of a nonclinical laboratory study shall have the education,training and experience, or combination thereof, to enable that individual to perform their assigned functions. They will also need to comply with Good Laboratory Practices (GLP), and all regulatory requirements applicable to the position. They will need to develop, revise, review and implement Standard Operating Procedures {SOPs) as applicable to the position. The Associate Scientist will need to understand and incorporate the information contained in the Employee Handbook into day to-day job performance and strive to demonstrate the Company's values in all work-related activities. They'll need to provide technical and scientific leadership in the area of analytical chemistry. This role requires them to plan and execute projects, identify and acquire the necessary facilities equipment and procedures for research projects by performing the below duties. | 5/17/2024 |
| 2830 | Alta Sciences Everett, WA Research Associate - Flow Cytometry Associate degree in scientific discipline. Exp: 6 months |
As a Research Associate I, you will be at the forefront of groundbreaking research, contributing to the success of our laboratory through diverse responsibilities that go beyond the ordinary. Engage in hands-on activities such as equipment maintenance, supply stocking, and general cleaning while supporting our Flow Cytometry team. | 5/17/2024 |
| 2831 | Alta Sciences Everett, WA Research Associate II - Biomarker Associate degree in scientific discipline. Exp: 6 months |
As a Research Associate II, you will be at the forefront of groundbreaking research, contributing to the success of our laboratory through diverse responsibilities that go beyond the ordinary. Engage in hands-on activities such as equipment maintenance, supply stocking, and general cleaning while supporting our Biomarker assay team. | 5/17/2024 |
| 2832 | Alta Sciences Scranton, PA Research Associate - Laboratory Animals BS/BA in a scientific discipline preferred. Exp: 0-2 years |
Do you love working with animals? Do you want to contribute to advancing human health science research? Do you like to work in small teams? Altasciences is seeking Research Associates at all levels of experience that have a passion for scientific research. In this position your focus will be working directly with animals in the collection of data and in support of the development of human medicine. You will perform technical procedures to support advancements in pharmaceutical development. In this position you will learn and perfect complex procedures including learning the skills to operate laboratory equipment, specimens collection techniques and data acquisition. At Altasciences Preclinical Services, we work with many different animal models: mice, rats, non-human primates, swine and canine and you will have the opportunity to become a proficient, highly skilled expert in this field. Multiple shifts available. | 5/17/2024 |
| 2833 | Alta Sciences Everett, WA Research Associate PCR - Laboratory Sciences Associate degree in scientific discipline. Exp: 6 months |
As a Research Associate III, you will be at the forefront of groundbreaking research, contributing to the success of our laboratory through diverse responsibilities that go beyond the ordinary. Engage in hands-on activities such as equipment maintenance, supply stocking, and general cleaning while supporting and executing data collection activities involving qPCR, ddPCR, and DNA isolation, . | 5/17/2024 |
| 2834 | Alta Sciences Columbia, MO Research Associate II, Laboratory Sciences Associates/Bachelor’s degree in Immunology/ Biology/ Chemistry or equivalent scientific discipline. Exp: 1-3 years |
The Research Associate II, Laboratory Sciences role works independently in the day-to-day laboratory operation, collection, and review of data for the Laboratory Sciences department. Support and perform data collection activities including ligand binding assays, and/or flow cytometry, and/or cell-based assays, and/or mass-spectrometry, and/or as assigned. Participates in the creation of study worksheets, SOPs and other documents as assigned. Provides support for general laboratory equipment and maintenance as assigned. | 5/17/2024 |
| 2835 | Alta Sciences Everett, WA Research Associate I - Small Animal Unit BS/BA in a scientific discipline preferred. Exp: 0-2 years |
Do you love working with animals? Do you want to contribute to advancing human health science research? Do you like to work in small teams? Altasciences is seeking Research Associates at all levels of experience that have a passion for scientific research. In this position your focus will be working directly with animals in the collection of data and in support of the development of human medicine. You will perform technical procedures to support advancements in pharmaceutical development. In this position you will learn and perfect complex procedures including learning the skills to operate laboratory equipment, specimens collection techniques and data acquisition. At Altasciences Preclinical Services, we work with many different animal models: mice, rats, non-human primates, swine and canine and you will have the opportunity to become a proficient, highly skilled expert in this field. Multiple shifts available. | 5/17/2024 |
| 2836 | Aluna Alameda, CA Scientist I - Research and Development BA/BS degree in Biochemistry, Molecular Biology, Microbiology or related field. Exp: 1-3 years |
Alveo Technologies is looking for a Research and Development Scientist 1 to support R&D efforts of projects in disease detection. A successful candidate will assist in planning and executing protocols, and conducting experiments at the bench to meet objectives. The candidate should be able to review, understand and follow the instructions, protocols and SOPs provided by R&D. | 5/17/2024 |
| 2837 | Alvogen Norwich, NY Quality Systems Specialist I Level I: Associate or Bachelor of Science in Chemistry, Life Science, Engineering or combination of training, education, and experience that is equiva Exp: 1 - 3 years |
The Quality Systems Specialist provides system administration and support of daily quality activities to ensure compliance with global regulatory requirements and guidelines (FDA, ICH, EU, WHO, etc.). | 5/17/2024 |
| 2838 | Alvogen Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline. Exp: 0-3 years |
The Quality Control Chemist I / Microbiologist I: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. | 5/17/2024 |
| 2839 | Amber Bio San Francisco, CA Research Associate Bachelor’s or Master’s degree in Biology, Biochemistry, Chemical Engineering, Biological Engineering, or a related field. Exp: 1 year |
Responsibilities: ● Work in a highly collaborative team focused on advancing our gene editing platforms. ● Support technology development strategy and design/build/test improved systems. ● Support engineering and characterization of editing systems with high-throughput experimentation. ● Maintain detailed, well-organized, and timely documentation of experiments and data. ● Effectively analyze and present data, and communicate research plans and timelines to the core team. ● Live Amber Bio’s core values of being biologically inspired, being honest and rigorous about our research, and fostering a supportive environment. | 5/17/2024 |
| 2840 | Amplify Bio West Jefferson, OH Asst./Associate Scientist, Analytical Sciences Bachelor’s degree in molecular biology, Biochemistry, Immunology, Molecular Genetics, or related field. Exp: 1 year |
AmplifyBio is currently seeking to hire an Assistant/Associate Scientist to join our growing Analytical Sciences team! The Assistant/Associate Scientist is responsible for performing analytical testing using a variety of cellular and/or molecular biology analysis platforms. Level of position and title will be based on experience and will report to a supervisor or senior scientist of Analytical Sciences. | 5/17/2024 |
| 2841 | ANI Pharmaceuticals Baudette, MN Quality Assurance Specialist Bachelors degree is required. Chemistry, medical technology, microbiology preferred. Exp: 1-2 years |
This position is responsible for providing support to the Manufacturing and Packaging Operations to ensure relevant procedures are followed and meet GMP requirements. This includes, but is not limited to the following: 2nd Shift Monday -Friday 3:15 pm to 11:15 pm | 5/17/2024 |
| 2842 | ANI Pharmaceuticals Baudette, MN Quality Control Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: QC Chemist – 1-3 years experience |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 5/17/2024 |
| 2843 | Aphena Pharma Easton, MD Manufacturing Engineer BSME or equivalent experience. Exp: 1+ years |
Aphena Pharma Solutions is looking for a Manufacturing Engineer to join our team in Easton, MD! Aphena Pharma Solutions is a dynamic pharma solutions provider focused on contract packaging, repackaging and manufacturing for the pharmaceutical, OTC, dietary supplement, animal health and medical device marketplaces. | 5/17/2024 |
| 2844 | Appia Bio Culver City, CA Research Associate I/II MS in Biology or related major. Exp: 0-4 years |
We are seeking a creative and driven Research Associate I/II ready to take on the challenge and opportunity presented by the frontiers of creating novel engineered cell therapies. The individual will be part of the Molecular Biology team and support the efforts to generate and deliver critical gene expression plasmids and lentivirus preparations. The individual will primarily be working directly with an Appia Bio Scientist and will be required to work both independently and as a team in a fast-paced environment to support ongoing discovery projects. The Research Associate I/II will join a culture of intellectual rigor and collegiality that has been built at Appia. | 5/17/2024 |
| 2845 | Applied Medical Rancho Santa Margarita, CA Plastics Process Engineer II Bachelor’s degree in Polymer, Materials, Plastics, or Manufacturing Engineering (or equivalent). Exp: 1-2 years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. As a Plastics Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. | 5/17/2024 |
| 2846 | Aptitude Medical Santa Barbara, CA Research Associate Bachelor’s degree or Master’s degree in a relevant discipline. Exp: Entry Level |
We are seeking to hire multiple capable and driven entry-level Research Associates to join our tight-knit research and development team. In this position, you will be working closely with a cross-functional team of mission-driven scientists and engineers to drive the invention and development of novel diagnostic products. | 5/17/2024 |
| 2847 | AAVIS Pharmaceuticals Hoschton, GA Quality Control Chemists (Hoschton, GA) Master’s Degree in Chemistry, Analytical Chemistry, or Pharmaceutical Science. Exp: 1+ years |
Develop and optimize quality control methods for drug product and drug substances; Perform testing of raw materials, intermediates and finished product using HPLC/Empower, GC, Dissolution apparatus/Autosampler, UV/Vis, and FTIR; Perform routine testing of residual solvents for raw materials and finished products; Develop and perform method validation and method transfer for ANDA and QC methods for Assay, Dissolution, Impurities, and residual solvents per USP and ICH guidelines; Calibrate and troubleshoot HPLC system, Dissolution, PH meter and KF apparatus; Perform wet chemistry tests, including LOD, pH, titration, residue on ignition and Heavy metals in compliance with cGMP and cGLP. | 5/10/2024 |
| 2848 | Abbott Minnetonka, MN Quality Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Minnetonka, MN location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Quality Engineer I is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support. | 5/10/2024 |
| 2849 | Abbott Sylmar, CA Mechanical Development Quality Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Mechanical Development Quality Engineer I assures new or modified products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs | 5/10/2024 |
| 2850 | Abbott Sylmar, CA Development Quality Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Development Quality Engineer I assures products, processes, and quality records conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient safety and meeting business needs. | 5/10/2024 |
| 2851 | Abbott Temecula, CA Associate Engineer - Product Performance Bachelor's degree. Exp: 0-2 years |
In this role you will identify, analyze, investigate, monitor and document patterns and trends in post marketing surveillance data as part of the CAPA system. Analyze and investigate product complaints from the field as part of post market surveillance requirements. Communicate and educate management, R&D, marketing, sales organization and other departments, as well as external customers about product performance. Ensure that information and insight gained from the investigations and corrective actions is fed back to the R&D and marketing organizations as part of the risk management and design input systems. Develop Post Market Surveillance Plans and provide engineering support for complaint investigation readiness of new products. | 5/10/2024 |
| 2852 | Abbott Sylmar, CA Risk Management Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Risk Management Engineer I works closely with development/manufacturing/quality engineering to establish and ensure compliance and quality for product related risk management documentation. Ensure risk management assessments and evaluations for products conform to established standards and agency regulations. | 5/10/2024 |
| 2853 | Abbott Pleasanton, CA Systems Engineer I Bachelor’s Degree in Engineering (Mechanical, Computer, Electrical, or Software), Computer Science, or related discipline. Exp: 6 months’ |
We are recruiting a Systems Engineer to join our Abbott Heart Failure team in Pleasanton, CA, where we are focused on helping people with heart failure manage their health to ultimately change and save lives. The engineer will be primarily working on the CardioMEMS HF portfolio, which remotely monitors changes in pulmonary artery (PA) pressure, which is used to prevent worsening heart failure, lower heart failure mortality rates, and improve quality of life for our heart failure patients. Systems engineering defines, designs, tests, and integrates components, disciplines, and products within the CardioMEMS HF System, including implantable sensors, external reader systems used by clinicians and patients, mobile application software, and cloud-based web applications. The System Engineer will help execute tasks during design change projects and development of next generation products, including requirements definition and management, design documentation, and system testing, verification, and validation. | 5/10/2024 |
| 2854 | Abbott Minnetonka, MN R&D Engineer I Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, biological sciences, medical/clinical science or equivale Exp: 1+ years’ |
As R&D Engineer I, at our Plymouth, MN or St. Paul, MN location, you will be part of our Electrophysiology (EP) product development team focused on delivering the future in diagnostic, imaging, and ablation therapy catheters. In Abbott’s Electrophysiology (EP) division, we’re advancing the treatment of heart and vascular disease through breakthrough medical technologies, allowing people to restore their health and get on with their lives. | 5/10/2024 |
| 2855 | Abbvie North Chicago, IL Veterinary Technician AS/BS degree. CVT required. Exp: 0-4+ years |
The Veterinary Technician carries out daily activities in the vivarium and provides clinical nursing care and research support for lab animals. Works independently on weekends and holidays. Contributes to specific projects in support of Comparative Medicine initiatives. Provides exemplary animal care. Adheres to all department and AbbVie regulatory expectations, as well as USDA and FDA regulations. Provides veterinary care in support of the AbbVie drug discovery and development process. | 5/10/2024 |
| 2856 | Abbvie North Chicago, IL Associate Scientist I/II – DMPK-BA: Drug Metabolism, Pharmacokinetics, and Bioanalysis Master’s Degree or equivalent education. Exp: 0+ years |
Quantitative, Translational & ADME Sciences Department at AbbVie has an open position for an Associate Scientist II position in North Chicago, IL. The successful candidate will be responsible for non-regulated quantitative LC-MS/MS bioanalysis of small molecules from in vivo and in vitro samples, including data analysis and interpretation. | 5/10/2024 |
| 2857 | Abbvie North Chicago, IL Associate Scientist II/ Scientist I - Process Chemistry MS degree in chemistry. Exp: 0+ years |
Process Research and Development is responsible for inventing and executing the chemical processes and preparing active pharmaceutical ingredient (API) to enable clinical trials, toxicology studies and drug product development for Abbvie’s pre-clinical and clinical candidates. We create valuable intellectual property through composition of matter, chemical processes, and technology resulting in a cost-effective commercial manufacturing process. We develop the supply chain for APIs, prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We seek a highly motivated scientist with strong synthetic skills to work under the mentorship of a supervisor and to work in a multi-functional team environment. Opportunities may also exist to contribute to high-throughput experimentation, automation, and data science. | 5/10/2024 |
| 2858 | Abbvie South San Francisco, CA Associate Scientist II orScientist I, CMC Drug Substance Cell Line Development Group Associate Scientist II - Master’s Degree or equivalent education. Exp: 0+ years |
The Development Sciences Biologics CMC Drug Substance Cell Line Development Group in South San Francisco, CA is seeking a Scientist to join a talented and collaborative team developing CHO cell lines for GMP applications. In this laboratory position, the candidate will perform hands-on molecular characterization studies in a well-supported and dynamic environment to help advance novel therapies to human clinical studies. The work will encompass molecular, cellular, and bioprocess development studies relating to the generation and characterization of optimized CHO cell lines for production of our pipeline candidates. | 5/10/2024 |
| 2859 | Abbvie Worcester, MA Associate Scientist or Scientist I, Recombinant Production BS or MS in biology or related field. Exp: BS: 0-5+ years; MS: 0-2+ years |
Discovery Biotherapeutics at AbbVie is seeking a highly-motivated research scientist to join a dynamic team supporting biologics drug discovery. This position will impact projects through purification and characterization of biopharmaceutical products such as monoclonal antibodies in high throughput. The ideal candidate has direct experience with mammalian tissue culture, protein purification, proficiency in standard chromatography techniques, protein characterization (e.g., MS, SEC), and binding assays (e.g., ELISA and flow cytometry). The applicant should be able to analyze, document, and report data. She/he should possess excellent communication skills and be comfortable presenting in group settings. | 5/10/2024 |
| 2860 | Abeona Therapeutics Cleveland, OH Associate, Quality Control BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline. Exp: 1 to 4 years |
The Quality Control Associate performs routine laboratory activities in support of GMP testing for Quality Control. Testing includes raw material, packaging components, in-process and finished product. Interacts with employees internal and external to Quality Control. | 5/10/2024 |
| 2861 | Absci Vancouver, WA Laboratory Technician Bachelor’s degree in Molecular Biology, Biochemistry, Microbiology, or a related discipline. Exp: 1+ years |
The Laboratory Technician will join the NGS Development team and support innovative research that advances Absci’s proprietary Drug Creation PlatformTM. The NGS team is integral to the success of most projects at Absci, and this role will involve delivering NGS results for library screens and strain construction. Primary responsibilities include providing core support to sequencing and analysis activities. The individual will work closely with other members of the NGS team in day-to-day sample preparation and operation and maintenance of Illumina and PacBio instruments. The individual should be able to master new laboratory skills rapidly and will take on additional technical responsibilities outside of the NGS team. This position will require the ability to work a weekend shift as needed. We seek candidates who are passionate about building a collaborative, multidisciplinary company culture and committed to making a transformative impact on our industry. To be successful in this role, the candidate should be a team player, have an innovative mindset, possess applicable technical experience, and be excited about working in a dynamic startup environment. An ideal candidate will demonstrate initiative and follow-through, a passion for scientific advancement, and a strong commitment to excellence. | 5/10/2024 |
| 2862 | Absci Vancouver, WA Research Associate II - Disease Biology Senior Research Associate: MSc in biology, cell biology, immunology or a relevant field. Exp: 1+ years |
As part of the Disease Biology Team, you will work on engineering cell lines for various programs and contribute to the development and optimization of cell-based assays, including, but not limited to, ligand-binding potency, cellular uptake, cytotoxicity, ADCC, CDC, ADCP, and proliferation assays. This role requires experience with mammalian cell culture techniques and understanding mechanism of action (MOA) assays. This position requires strategic thinking and a high level of collaboration across multidisciplinary teams within Absci. It also requires excellent communication, technical, and organizational skills and demonstrated success in delivering under tight timelines. Individuals who enjoy working with a sense of urgency and thrive in a dynamic team and high-performance culture will be successful and thrive in this role. | 5/10/2024 |
| 2863 | Accelerated Diagnostics Tucson, AZ Research Associate (Pilot Lab) BS in a scientific discipline. Exp: 1 year |
Accelerate Diagnostics is seeking a motivated Research Associate who would like to gain hands-on experience in an R&D pilot lab supporting antimicrobial susceptibility test (AST) assay development. The successful candidate will be passionate, well-organized, detail-oriented, and work independently as well as in a team environment. The candidate will spend approximately 70% of their time on basic laboratory techniques and the remaining 30% on assisting technical staff with routine lab and office work including equipment maintenance and cleaning, data entry and data management. The work schedule is Monday-Friday, 8:00 am - 5:00 pm. | 5/10/2024 |
| 2864 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology. Exp: 0-3 years |
The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. | 5/10/2024 |
| 2865 | Astrazeneca Waltham, MA Research Associate Bioscience Immunology, Early Respiratory And Immunology BS or MS degree in biology, immunology or a relevant discipline. Exp: 1 year |
As a part of our growing Immunology Bioscience team within the Early R&I department, we are seeking a highly motivated scientist with diverse laboratory skills to join our collaborative team. This candidate would ideally have experience in immunology or related disciplines such as biology, biomedical engineering, virology, genetics or microbiology. This is a lab-based position, and the role will be based in Waltham, Massachusetts within AstraZeneca’s state-of-the-art laboratories where you will follow the science to help drive innovation and advance medicine to help improve patient lives. This position offers a unique opportunity to work in a dynamic and innovative environment developing your career at the interface of research and drug discovery. | 5/10/2024 |
| 2866 | Astrazeneca Gaithersburg, MD Associate Scientist - Viral Clearance Bachelor’s degree. Exp: 1 – 2 years |
This role will focus on viral clearance, part of the protein purification development function in the PAS department. The major responsibilities include: Design and execute studies to demonstrate virus removal or inactivation capabilities for protein purification unit operations, initially with guidance and gradually become independent. In collaboration with existing team members, plan studies, manage logistics, documentation, data verification and interpretation, report writing, and participate in regulatory submissions. Make periodic presentations in group meetings, project team meetings, and in one-on-one situations. Support purification process development, technology transfer to manufacturing sites, and production incident resolution as appropriate. Participate in new technology evaluations | 5/10/2024 |
| 2867 | Astrazeneca Lexington, MA Engineer - Downstream, Viral Vector Product Development BS or MS degree in Biological Engineering, Chemical Engineering, Biochemistry, or related discipline. Exp: 0-3 years |
The candidate contributes to the Viral Vector Product Development group through the design and execution of experiments based around downstream AAV (Adeno-Associated Virus) manufacturing processes. They will assist the purification team to generate, interpret, and present experimental data to inform and recommend process operating conditions with the goal of developing a robust and scalable manufacturing process. They will additionally draft documentation and provide expertise to assists in scale-up and tech transfer to clinical/commercial manufacturing facilities as well as submission of regulatory filings. | 5/10/2024 |
| 2868 | Astrazeneca Lexington, MA Engineer - Upstream, Viral Vector Product Development BS or MS degree in Biological Engineering, Chemical Engineering, Biochemistry, or related discipline. Exp: 0-3 years |
The candidate contributes to the Viral Vector Product Development group through the design and execution of experiments based around upstream AAV (Adeno-Associated Virus) manufacturing processes. They will assist the upstream team to generate, interpret and present experimental data to inform and recommend process operating conditions with the goal of developing a robust and scalable manufacturing process. They will additionally draft documentation and provide expertise to assist in scale-up and tech transfer to clinical/commercial manufacturing facilities as well as submission of regulatory filings. | 5/10/2024 |
| 2869 | Astrazeneca New Haven, CT Engineer II, Injectable Drug Product Development MS degree in Biochemistry, Chemistry, Chemical Engineering or related field from an accredited university. Exp: 1+ years |
The Engineer II will design and implement experiments to develop injectable drug product formulations and process characterization studies, including analyzing samples and authoring technical reports. Work on an impactful dynamic team and routinely collaborate to innovate with other members of Injectable Drug Product Development as well as other groups in Product Development and Clinical Supply! | 5/10/2024 |
| 2870 | Astrazeneca Frederick, MD Production Technician I -Day Shift BS/BA Degree in STEM field. Exp: 1+ years |
In this role, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also train with a qualified Technician on activities related to operating process equipment with the requirement of qualification. Additionally, you will follow and execute cGMP documentation, utilize Manufacturing Execution systems (MES), contribute to problem-solving activities for non-routine activities on the production floor, and participate in continuous improvement activities for Manufacturing. Adherence to AstraZeneca values and behaviors is expected. | 5/10/2024 |
| 2871 | Astrazeneca Gaithersburg, MD Associate Specialist (Clinical Biologics) Bachelor's degree. Exp: 0+ years |
As an Associate Specialist in the Clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities. Under the supervision of highly trained personnel, you will gain the process knowledge and abilities to perform large scale clinical development activities. You will join a collaborative and driven team in an extraordinary biopharmaceutical company. | 5/10/2024 |
| 2872 | Active Motif Carlsbad, CA Research Associate I-III RA I: Bachelor's degree in Biological sciences (in Molelcular Biology, Genetics, Life Sciences or related fields). Exp: 0-1 year |
Supports Epi-Services customer projects received by Operations & Services Team Performs next generation sequencing (NGS) lab bench work assigned in a time dependent, quality dependent manner Executes assigned lab bench experiments in a time dependent manner and quality dependent manner Train and follow SOP for each Assay Service Record, document and store data & results as per the SOP/receipt and logging of samples in LIMS tracker Ensure, contribute and support team goals achievements Performs regular clean-up of the lab bench space / equipment utilized Performs and follows safety requirements as outlined Keeps detailed record of lab experiments, logs of instruments utilized Sets up and follows quality control requirements Contributes and supports Group Leader with customer projects data analysis Will perform up to 4 different Assay Services with varying sample batch sizes Other duties as required and/or assigned | 5/10/2024 |
| 2873 | Adapt Immune Philadelphia, PA Manufacturing Cell Therapy Specialist Bachelor degree in a cell biology, bioengineering or medical technology related field, or equivalent experience is required. Exp: 1+ years’ |
This role will provide support for the manufacturing of gene modified autologous T-cell product at our manufacturing site in the Philadelphia Navy Yard. The Specialist will perform cell processing activities, media formulation, product sampling, and other manufacturing needs as necessary, commensurate with the level of training and experience of employee. Work is primarily in Grade B and Grade C aseptic manufacturing environment, but may also include support of process development runs in the Manufacturing Science and Technology laboratory. | 5/10/2024 |
| 2874 | Adaptive Biotech Seattle, WA Accessioning Specialist II Bachelor’s degree in Biology, Molecular Biology, Immunology or Chemistry. Exp: 1+ years |
The Biological Sample Management Accessioning Specialist II will be an entry level lab operations team member who is able to accession for the clinical or research accessioning teams or assist in sample management. This role is expected to spend approximately 90% of their time inside the lab and 10% of their time working on various tasks assigned by the department. A successful Accessioning Specialist II will complete the responsibilities described below while working to support clinical and research sample management within Molecular Laboratory Operations. Shift: Tuesday - Saturday 9:30am-6:00pm PT | 5/10/2024 |
| 2875 | Adaptive Biotech Seattle, WA Material Handler II BS/BA degree preferred. Exp: 1 year |
As a Material Handler II at Adaptive, you’ll be responsible for assisting the clinical laboratory operations and research labs maintain the right levels of inventory. We are seeking team-oriented and energetic individuals who have previous experience in highly regulated environments. Material Handlers reconcile receipts, move, store, and distribute various non-hazardous and hazardous materials, laboratory components, and business supplies. Working with closely related departments, you’ll conduct an array of activities to replenish raw materials and supplies where they are needed. | 5/10/2024 |
| 2876 | Adaptive Biotech Seattle, WA Research Associate I Bachelor’s degree in biology, molecular biology, immunology, or similar discipline. Exp: 0-3 years |
Adaptive is seeking a Research Associate I with an aptitude for learning to join our dynamic and collaborative R&D Operations team. You will join the high throughput molecular lab team to aid in the development of new and existing assays for cellular and computational biology research across Adaptive. In this job, you will master a variety of molecular biology techniques and participate in immune system profiling by next generation sequencing jointly with other researchers and computational biologists. As such, high attention to detail and willingness to learn is crucial for success in the role. | 5/10/2024 |
| 2877 | Adare Pharma Solutions Vandalia, OH 3rd Shift QC Chemist Bachelors Degree in Chemistry or related field. Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 5/10/2024 |
| 2878 | Adhezion Mansfield, TX Process Engineer BS Degree in Chemical or Mechanical Engineering. Exp: 1+ years |
The Process Engineer will report to the Plant Manager. This position will lead the plants Process Improvement and EHS programs and be responsible for driving manufacturing productivity by improving process efficiencies, reducing wastes, improving quality, and increasing capacities as well as ensuring profitable growth through successful new product commercialization. Key processes in this adhesives and sealants manufacturing facility include solids conveying, mixing, compounding, chemical reactions, and packaging. Engineer will be coming in on the ground floor of a newly installed wood flooring urethane production line, with the ability to work with a diverse group of experienced operators in a positive culture environment. | 5/10/2024 |
| 2879 | Adimab Lebanon, NH Research Associate - Mammalian Cell Culture B.S. Exp: 1-3+ years |
We are seeking a Research Associate with experience in mammalian cell culture and protein expression to join our team. This role will support Adimab's novel antibody discovery, maturation, and production platform and closely interface with the Antibody Discovery, Protein Analytics, Molecular Core, and Computational Biology teams. | 5/10/2024 |
| 2880 | Adma Biologics Boca Raton, FL QA Specialist I - Product Release Bachelor's Degree required. Exp: One to two years |
The QA Specialist I - Product Release will have the primary responsibility consisting of the review of controlled documents for accuracy and completeness prior to Quality Assurance (QA) release of product. | 5/10/2024 |
| 2881 | Adma Biologics Boca Raton, FL Technician III, Manufacturing Fractionation - Night Bachelor's degree. Exp: 1+ years |
The Technician III, Manufacturing Fractionation - Night Shift position is under direct supervision of the Group Leader. This experienced position is responsible for the manufacture of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. | 5/10/2024 |
| 2882 | Adma Biologics Boca Raton, FL Technician II - Manufacturing Fractionation - Night Bachelor's degree. Exp: 1+ years |
The Manufacturing Technician II, Fractionation - Night Shift position is under direct supervision of the Group Leader. This experienced position is responsible for the manufacture of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. | 5/10/2024 |
| 2883 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences. Exp: BS: 1-3 years ; MS: 1 year |
Admera Health is looking for an Associate Scientist I/II to join our growing team! • Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing • Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. • Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. • Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. • Strict recordkeeping of all laboratory procedures. • Continue acquiring next generation sequencing knowledge to support molecular biology techniques. • Collaborate within the group and cross departmental to achieve goals. | 5/10/2024 |
| 2884 | ACDBio Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex Assays. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 5/10/2024 |
| 2885 | ACDBio Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 year |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 5/10/2024 |
| 2886 | ACDBio Newark, CA Senior Research Associate, PAS MS in molecular biology, biochemistry, cell biology or related field. Exp: 0-2 years |
he Senior Research Associate (SRA) will serve as a key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic sponsors to detect RNA targets of interest. An additional critical work component will be the application of immunohistochemistry (IHC) to look for specific protein targets. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. It is expected that the Sr. Research Associate will independently collect and interpret data based on project expectations, which has implications for many downstream applications, such as biomarker validation and cell and gene therapy. The SRA will also be expected to independently utilize available resources for any required troubleshooting and communicate clearly with sponsors through both electronic mail and teleconference channels. The SRA must also coordinate with internal research and development (R&D) team to learn new techniques quickly and be able to adapt to shifting priorities in a fast- paced and growing start-up environment. | 5/10/2024 |
| 2887 | EyeCRO Oklahoma City, OK Research Associate I Bachelor's degree in a biology related field. Exp: 1 year |
We are looking for a Research Associate to join our team. The ideal candidate will be responsible for participating in a wide variety of animal-based activities and performing routine wet chemistry. This position plays a critical role in our mission to support groundbreaking scientific research and development. We highly value individuals who thrive in a dynamic team setting. Our team's success is built on a foundation of mutual support, shared goals, and a commitment to excellence. | 5/2/2024 |
| 2888 | Frontida BioPharm Vandalia, OH 3rd Shift QC Chemist Bachelors Degree in Chemistry or related field. Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 5/2/2024 |
| 2889 | Frontida BioPharm Vandalia, OH 3rd Shift QC Chemist Bachelors Degree in Chemistry or related field. Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 5/2/2024 |
| 2890 | Fujifilm Diosynth College Station, TX Manufacturing Technician II Associates degree. Exp: one (1) year |
Summary: The Manufacturing Technician III will work directly with a range of technologies. Dependent Upstream Unit: Single-Use Cell Culture Vessels/Bioreactors up to 2000L Bacterial Fermentation Culture Vessels up to 2000L Alpha Wasserman Continuous Flow Centrifuge Disposable Magnetic Mixing Bags and Totes Cell Expansion and Propagation Banking/Cryopreservation of Cell Lines and Viruses Hyperstack, Cellstack, and other Adherent Cell Technologies Plate counting, microscopic examination Monitor cultures, take samples, turn-around of bioreactor and fermenters, sterilization, and inoculation Downstream Unit: Medium to Large-scale filtration systems including Tangential Flow Filtration (TFF), Hollow Fiber Tangential Flow Filtration (HFTFF), Nanofiltration and depth filtration Medium to Large-scale Chromatographic systems (ÄKTA). Pre-Packed Columns from 1L to 100L Single use mixing systems (Pall & GE) Single Use connectivity types such as GE DAC and Colder AseptiQuik Bulk filling Aseptic process simulation and drug product filling Plate counting, microscopic examination Alpha Wasserman Continuous Flow Centrifuge | 5/2/2024 |
| 2891 | Fujifilm Diosynth College Station, TX Quality Control Visual Inspection Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field. Exp: 1+ year |
Summary: The Visual Inspection Analyst I will be responsible for assisting the drug product visual inspection program at FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. External US Essential Functions: Perform visual inspection for Final Product Fills and Aseptic Process Simulations (APS) for AQL level inspections Participate in threshold study (POD) executions and training exercises for visual inspection Participate in particulate identifications and investigations, as required. Sub-visible particulate testing (USP <787>, <788> (Method 1 and Method 2), <789>), as appropriate Secondary functions could include: environmental monitoring (Total Air, Viable Air and Viable Surface) in a cleanroom/controlled environment, plate count enumeration and characterization, routine QC laboratory cleaning, management of inventory items for the laboratory Ensure the lab is maintained (organized, clean, & properly supplied). Perform other duties as assigned. Required Skills & Abilities: Must be able to pass a visual acuity test given upon hire, with corrective lenses if necessary. Ability to follow safety procedures outlined in the Chemical Hygiene Plan. Good attention to detail and ability to utilize problem solving/trouble shooting skills. Good computer skills. Demonstrated written and oral communication skills. Ability to multi-task and prioritize work assignments with little supervision. Strong organization and analytical skills | 5/2/2024 |
| 2892 | Fujifilm Diosynth Holly Springs, NC Manufacturing Associate 3 - Drug Product BA/BS, preferably Life Sciences or Engineering. Exp: 1+ year |
This role as Manufacturing Dssociate 3 in Drug Product, will mainly include the operation of the filling line including all the related tasks. This role will support projects, which will influence the manufacturing processes for Drug Product Manufacturing. This includes, training new colleagues, maintaining compliance of cGMP documents and assisting in the qualification of equipment as well as all other aspects of the startup of the DPFG facility. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation. While in project phase, the schedule will be Monday-Friday during normal business hours. Upon transitioning to operations, this position will transition to a day or night shift that will be defined prior to the transition. During the project phase Contribute to the preparation for operational readiness related to bulk drug product manufacturing Possible assignments include, supporting projects related to procedure review and/or creation, development or transfer of manufacturing business processes and testing and commissioning support Travel up to 0-25% (international or domestic) may be required during the project phase In operations Lead, execute and document manufacturing processing steps and/or manufacturing support activities as well as process monitoring and control Perform in-process testing (pH, conductivity, visual inspection) Execute validation protocols according to cGMP Standard Operating Procedures (SOPs) Maintain training to perform all required manufacturing activities Assist and/or lead cycle counts and manage materials for the assigned manufacturing functional area Perform Operations for all aspects of filling line Assist the lead with tasks in manufacturing activities Assist with the coordination of daily shift activities This role requires shift work (weekend and potential for nights) Perform other duties as assigned | 5/2/2024 |
| 2893 | Waters Milford, MA Design Quality Engineer Minimum of a Bachelor’s degree in Engineering or Science related function. Exp: 1+ year |
This position will be responsible for concurrent quality engineering science activities associated with the consumables and lab automation product development business unit, on-market design change, risk management, quality systems and Waters requirements for columns, kits and chemistry products. Primary responsibility will be to provide chemistry/scientific and product support in the following areas: design controls, risk management, change control, post market review, quality planning, continuous improvement, establishment of appropriate requirements management and traceability. This is a Hybrid position based in Milford, MA | 5/2/2024 |
| 2894 | InBios International Seattle, WA Research Associate I A bachelor’s degree in a biologicals science. Exp: 1-2 years |
You have a biologicals, life sciences degree, academic or commercial lab experience with good simple buffer knowledge and experience and a firm scientific foundation, and you are eager to put your skills and knowledge to use in the commercial biotech assay research and development field. You also thrive in a fast-paced work environment where priorities and projects may change quickly. You are attentive and teachable and have a strong desire to learn new skills and you want hone those skills you have already begun to master under the supervision and instruction of the team’s lead scientist. You are a good teammate who is responsible and motivated and comfortable working closely in a team environment, where you openly share ideas and collaborate. You may or may not already have lateral flow immunoassay experience. (Prior experience with LFI is not required for the Research Associate I position.) | 5/2/2024 |
| 2895 | InBios International Seattle, WA Manufacturing Associate I - ELISA Bachelor’s degree with emphasis on life science OR Associate of Applied Science degree preferred but not required. Exp: 1-year |
We are searching for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other InBios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale ELISA diagnostic test components in a BSL-2 laboratory. If you are seeking an entry-level, full-time, on-site position where you can gain experience and grow at the forefront of medical diagnostic biotechnology, this is a great opportunity for you. | 5/2/2024 |
| 2896 | InBios International Seattle, WA Manufacturing Associate I- Rapid Spray (2nd Shift 3:30PM - 12:00AM) Bachelors degree in life sciences or a similar field. Exp: 1 year |
We have an immediate opening for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other InBios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale lateral flow diagnostic test components. If you are seeking an entry-level position with opportunities for experience and growth at the forefront of medical diagnostic biotechnology this is a great opportunity for you. This position operates on two schedules. This opportunity is for our 2nd shift, which is from 3:30 PM - 12:00 midnight Monday - Friday. | 5/2/2024 |
| 2897 | Pace Analytical Maplewood, MN Laboratory Technician Minimum requirement: Associate degree in science or equivalent laboratory experience. Exp: 1 year |
Join us as a Laboratory Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This candidate will be responsible for maintaining the lab spaces and supplies to support research and development laboratories. This includes maintaining equipment, supplies, and lab cleanliness that support the development of a variety of healthcare products. This role may include basic solution and sample preparation. | 5/2/2024 |
| 2898 | Pace Analytical Maplewood, MN R&D Lab Tech B.S. in a chemistry, biology or related area of study. Exp: 1+ years |
Join us as an R&D Lab Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. A candidate for this position will have excellent lab skills across a variety of techniques to support a research lab focusing on development of medical adhesives and other devices | 5/2/2024 |
| 2899 | Pace Analytical Maplewood, MN Bioanalyst B.S. in molecular biology, biochemistry, biology, chemistry or related science. Exp: 0+ years |
Join us as a Bioanalyts, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This candidate will be responsible for performing bioassays and application development to support biopharmaceutical filtration devices. These analyses include ELISAs, PCR, DNA and more that support cell culture production. In addition the candidate will be supporting the development of new applications of current filtration products. Join us as a Bioanalyts, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. | 5/2/2024 |
| 2900 | Pace Analytical Maplewood, MN Physical Properties Technician - Entry Level Bachelors degree in a science field. Exp: 0+ years |
Join us as a Physical Properties Technician, where you’ll put your love of science to work in the Scientific Insourcing Solutions division. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The Scientist will prepare and test samples in the lab for adhesive products, and assist with lab maintenance | 5/2/2024 |
| 2901 | Pace Analytical Maplewood, MN Product Engineering Techician B.S. in Chemistry, Biochemistry, Materials Science or related science. Exp: 1+ years |
Join us as an Engineering Product Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This position will actively support the testing of healthcare products crucial to patient’s safety efforts within the healthcare industry. This role includes performing lab-scale polymerization reactions, coating adhesive solutions into films, and physical properties testing. Work is performed as part of a team in a fast-paced environment | 5/2/2024 |
| 2902 | Pace Analytical Maplewood, MN Laboratory Technician Minimum requirement: Associate degree in science or equivalent laboratory experience. Exp: 1 year |
Join us as a Laboratory Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This candidate will be responsible for maintaining the lab spaces and supplies to support research and development laboratories. This includes maintaining equipment, supplies, and lab cleanliness that support the development of a variety of healthcare products. This role may include basic solution and sample preparation. | 5/2/2024 |
| 2903 | Pace Analytical Brooklyn Park, MN Microbiologist Bachelor's degree in Microbiology, Biology or a related discipline required. Exp: 1 year - 4 years |
Join us as a Microbiologist, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The main function of the QC Microbiologist is to perform supportive activities for general lab readiness, conducting critical biological tests, and following SOPs to perform methods using analytical skills and understanding of biological and chemistry techniques and principles. Note: This position is expected to last 9 months up to 1 year. Note: Training will occur for 2-3 weeks standard 8-hour days M-F. Regular schedule will be Saturday - Tuesday, 10 hour days | 5/2/2024 |
| 2904 | Vigene Biosciences Rockville, MD QC Associate I - Environmental Monitoring - 4 - 10 hour shifts, Thursday - Sunday from 8am - 6pm 1 B.S in Biology or related field. Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Associate I – Environmental Monitoring will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 5/2/2024 |
| 2905 | Vigene Biosciences Malvern, PA Technician II Mammalian Cell Banking Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 1 to 2 years |
Under direct supervision, responsible for performing basic daily laboratory and clean room tasks as they relate to the operations performed within the Manufacturing department, including mammalian cell banking and vaccine preparation activities, data analysis and writing client batch records and SOPs. | 5/2/2024 |
| 2906 | Vigene Biosciences Malvern, PA Sample Processing Materials Technician Bachelor's degree (B.A./8.S.) or equivalent in scientific discipline preferred. Exp: 1 to 3 years |
Responsible for performing a wide variety of tasks involved in sample processing and inventory management of critical components, critical laboratory supplies, specialty reagents, client-supplied raw materials, and internal and external cell banks. Performs a variety of activities related to log in, sample processing, storage, shipping of stored materials and client support | 5/2/2024 |
| 2907 | Vigene Biosciences Memphis, TN Biomanufacturing Technician I - Shift C Tuesday-Friday: 11:30am-10:00pm EG AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
NOTE: This position is: Shift C: Tuesday thru Friday 11:30am - 10:00pm (Saturday, Sunday, Mondays off) The BioManufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 5/2/2024 |
| 2908 | Vigene Biosciences Wayne, PA Technician I Environmental Monitoring Bachelor's degree (B.S.) or equivalent in biology or related discipline. Exp: 0 to 1 year |
Responsible for performing daily laboratory tasks as they relate to the Environmental Monitoring and Contamination Control Department. | 5/2/2024 |
| 2909 | Vigene Biosciences Memphis, TN QC Specialist 1 Microbiology Bachelor's degree in biology or relevant scientific discipline preferred. Exp: 1 years |
The QC Specialist I for the QC Microbiology Department will be responsible for reviewing laboratory data, writing laboratory and environmental monitoring excursion reports, and executing simple tasks within projects/CAPAs/Change controls. The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success. | 5/2/2024 |
| 2910 | Pharmaceutical Calibrations and Instrumentation Indianapolis, IN Applications Engineer - FP/Sentinel - Indianapolis, IN Degree in engineering, mechanical preferred. Exp: 1+ years |
As an Applications Engineer you will assist our sales force with technical expertise for the design of fluid power systems and customer system integrations. This includes preparing hydraulic schematics, test procedures and recommend components. You will provide integral project management for these systems. | 5/2/2024 |
| 2911 | Boston Scientific Arden Hills, MN Analytical Chemist I - Extractables and Leachables Bachelor’s degree or higher in chemistry-focused field with aptitude for analytical chemistry. Exp: 1+ years |
The Analytical Chemist I will support chemical characterization (extractables & leachables) testing of medical devices. This role will involve significant hands-on laboratory work, including solution preparation and testing. The medical device products supported include products across the Boston Scientific portfolio. | 5/2/2024 |
| 2912 | Boston Scientific Arden Hills, MN R&D Technician II - 1st Shift Associates in Arts degree/diploma. Exp: 1 Year |
Executes and supports testing of implantable medical device batteries often involving specialized equipment in a laboratory environment during the design, development, and production life cycles of medical devices batteries. Your work will directly impact the quality and reliability of BSC products and improve the lives of our patients. You will be directly involved in characterizing and evaluating the performance of implantable medical device batteries. Take pride that the work you do helps save lives and improve the quality of life for millions of people around the world. | 5/2/2024 |
| 2913 | Boston Scientific Arden Hills, MN Manufacturing Tech II - 3rd Shift Associate in Arts degree/diploma. Exp: 1+ years |
Responsible for performing functions associated with all manufacturing operations, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components, subassemblies, and final assemblies. Determines and may assist in developing methods and procedures to control or modify the manufacturing process. Works with engineers in conducting experiments. | 5/2/2024 |
| 2914 | Boston Scientific Arden Hills, MN Manufacturing Tech II - 2nd Shift AA degree. Exp: 1 year |
Responsible for performing functions associated with all manufacturing operation, including manufacturing equipment support, calibration tasks, equipment optimization, OEE utilization. In battery manufacturing we have a diverse roster of equipment. You will support automation systems, electrical test equipment, laser systems, fixturing, vacuum systems, and much more. This is a great opportunity to further your technical career within a winning, people-oriented company. | 5/2/2024 |
| 2915 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Monday through Friday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. We have an exciting opportunity for a Research Technician I (Monday through Friday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 5/2/2024 |
| 2916 | Charles River Laboratories Ashland, OH Research Analyst I - Immunology Bachelor's degree (B.A. / B.S) or equivalent in laboratory science or related discipline required. Exp: Zero to two years |
We are seeking a Research Analyst 1- Immunology for our Safety Assessment site located in Ashland, OH. Essential Duties and Responsibilities: • Perform assays such as ELISA, multiplex, immunophenotyping, comet, and micronucleus. • Perform density gradient cell separations. • May act a lead/primary technician on basic studies. • Utilize micropipettes for all assays. • Perform study preparation activities including ordering supplies, preparing/verifying paperwork, and tube labeling. • Receive and log in reagents, solutions, and samples. • Prepare simple to complex lab solutions. • Assist in method development studies, method validation studies, and equipment validations as needed. • Operate, perform quality control and maintenance procedures on equipment such as microplate readers, plate washers, cell counters, multiplex instruments, flow cytometers, freezers, liquid scintillation counter, gamma counter, and eyewash stations. • Maintain clean work areas by cleaning dishes/glassware, wiping down countertops, and sweeping/mopping floor as needed. • Collect and record data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), protocols, and study plans. • Input, print, and edit basic to complex data. • Prepare materials for shipment and archival. • Review documentation for quality control. • Perform all other related duties as assigned. | 5/2/2024 |
| 2917 | Leica Biosystems Vista, CA Software Engineer (Hybrid) Bachelor’s in (completed or in progress) in computer science, software engineering, or similar. Exp: 0-2+ years |
The Software Engineer for Leica Biosystems will located in Vista, CA, is hybrid, and will report to a Senior Manager, Software Development. This Software Engineer is responsible for helping perform maintenance and make modifications on existing and new software products. | 5/2/2024 |
| 2918 | Genesis Therapeutics San Diego, CA Research Associate, Biochemistry B.S./M.S. in Biochemistry, Biology, or a related field. Exp: 1 year |
Genesis Therapeutics is pioneering artificial intelligence guided rational drug design to address severe unmet medical needs for patients. Our lab in San Diego is looking for a motivated and enthusiastic candidate to support in vitro biochemical assay screening efforts. You will be producing biochemical activity & binding data using various technologies that will help drive rapid progress in our drug programs across a variety of different targets. | 5/2/2024 |
| 2919 | Genoptix Ft Myers, FL; Tampa, FL; Nashville,, FL Clinical Laboratory Technologist Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences. Exp: one year |
As a Clinical Laboratory Technologist Dry Lab you will work under general supervision and you will be responsible for accurately performing highly complex laboratory testing procedures. You will determine acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. You will also analyze specimens, review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 5/2/2024 |
| 2920 | Genoptix Houston, TX; Ft Myers, FL; Tampa, F, TX Clinical Laboratory Technologist II Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences. Exp: one year |
As a Clinical Laboratory Technologist I Dry Lab you will work under general supervision and you will be responsible for accurately performing highly complex laboratory testing procedures. You will determine acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. You will also analyze specimens, review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 5/2/2024 |
| 2921 | Genoptix Aliso Viejo, CA Clinical Laboratory Technologist- Molecular Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences. Exp: one year |
As a technologist, you will work under general supervision. You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 5/2/2024 |
| 2922 | MEDTOX Raritan, NJ Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! Pay Based on Experience -- Starting @ 28.50/hour Sign-On Bonus of $5,000 ( External Candidates Only ) The work schedule for this position will be Sunday - Thursday 10:00 pm - 6:30 am | 5/2/2024 |
| 2923 | MEDTOX Holyoke, MA Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Holyoke, MA. In this position, you will work in a fast-paced, customer-focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! The work schedule for this position will be Tuesday - Saturday 10:00 pm - 6:30 am | 5/2/2024 |
| 2924 | MEDTOX Binghamton, NY Clinical Laboratory Technician Associate degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team Guthrie Lourdes Hospital in Binghamton, NY. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Pay Range: $20.40 - $40.14 + 10% shift differential on weekdays or 15% shift differential on weekends Work Schedule: 3x8 hour shifts: Weekdays, 3:00pm- 11:30pm and rotating weekends | 5/2/2024 |
| 2925 | MEDTOX Westborough, MA Clinical Laboratory Technologist - Molecular Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Pay Based on Experience -- Starting @ 26.00/hour Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, The Integrated Genetics Division of LabCorp is seeking a Molecular Technologist to join their Molecular Diagnostics team in Westborough, MA! In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, Real-time PCR, Sanger Sequencing, MLPA, Methylation PCR and Fragment Analysis to test for specific genetic diseases such as Cystic Fibrosis, Spinal Muscular Atrophy and Fragile X Syndrome to name just a few. Work Schedule: Sunday - Thursday, 7:00am - 3:30pm. | 5/2/2024 |
| 2926 | MEDTOX Lowell, MA Clinical Laboratory Technologist Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
$10,000 sign on bonus (external candidates only) Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team at Lowell General Hospital Saints Campus in Lowell, MA. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Work Schedule: Monday- Friday, 7:00am - 3:30pm & every 3rd weekend | 5/2/2024 |
| 2927 | Steris Mentor, OH Associate Scientist I Bachelor degree in Biology, Microbiology, Molecular Biology is preferred. Exp: 1-5 years |
Position Summary The Associate Scientist I will work in the Product Development team performing microbiology methodologies with several strains of BSL1 and BSL2 test organisms, including bacteria, fungi, and viruses. The position will require implementing established methodologies to evaluate the microbiocidal activity of disinfectants and sterilization processes. The position will also perform testing to develop and evaluate sterility assurance products (i.e. biological indicators). The position will require accurately maintaining, recording, and reporting test data. Additionally, applicant must possess the ability to perform and accurately document tasks according to established microbiocidal test standards, work instructions, and written protocols in a timely manner, while working both independently and within a team on multiple studies at different stages of the process. This position is located onsite in Mentor, OH. | 4/22/2024 |
| 2928 | Steris Richmond, CA Quality Engineer Bachelor Degree in Engineering or Computer Science Exp: 1+ years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR, and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems | 4/22/2024 |
| 2929 | Steris Spartanburg, SC Quality Analyst Bachelor's Degree Exp: 1-5 years |
The Quality Analyst is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. Responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting. | 4/22/2024 |
| 2930 | Stryker Portage, MI Design Engineer – Electrical, RISE B.S or M.S. in Electrical Computer Engineering, Electrical Engineering or related engineering discipline; we will only consider candidates with Decemb Exp: 0+ years |
Stryker, a global leader in medical technology takes great pride in their people, and that’s why we’re looking to expand our talent. As a result, we are looking for the best and brightest graduates to strengthen our team and drive our business going forward. The Rotational Intensive Specialized Experience (RISE) Program, which lasts 2 years and includes 4 six-month rotations, is designed specifically for highly talented engineers who are looking for exposure to and experience in different disciplines of engineering. Participants will be immersed into new product development (design engineering), quality, product testing, simulation, and so much more. Each individual’s rotations are tailored to fit their passion and skill sets along with current business needs. RISE engineers will not only gain a broad knowledge of our Research & Development functions but will also have the opportunity to attend additional leadership and personal development trainings, seminars, and product labs. The RISE Engineering program also offers exposure to senior leadership with end of rotation presentations, townhalls, and small group forums. Upon successful completion of the program, participants are eligible to apply to any open roles within Stryker. | 4/23/2024 |
| 2931 | Stryker Portage, MI Mechanical Engineer, R&D – Sustainment Bachelor’s Degree in Mechanical Engineering or related Exp: 0+ years |
Stryker is seeking to hire a Mechanical Engineer, R&D to support Medical’s Acute Care Product Engineering team. This role is onsite, in Portage, MI with the expectation to come into the office 4-5 days a week. Stryker Bed Frames Stryker Stretchers and Transport Chairs | 4/23/2024 |
| 2932 | WuXi Apptec San Diego, CA Research Associate III Master degree in Molecular and Cell Biology Exp: 0+ years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate III to support our in vivo pharmacology team for various projects. | 4/24/2024 |
| 2933 | WuXi Apptec San Diego, CA Research Associate Must have Master’s degree in Biochemistry, Cellular and Molecular Biology, Biomedical Engineering, or Biotechnology. Exp: 1+ years |
Research Associate (San Diego, CA) – Skills and knowledge in Biological Macromolecules, Protein/ligand Binding, Cell-cell Interactions, Gene Delivery, Stem Cells Engineering, Polymer Synthesis/processing. Perform assay in cell-based format and biochemical assays using Biological Macromolecules, Protein/ligand Binding, Cell-cell Interactions, Gene Delivery, and Mammalian cell culture; Perform compound management work; Perform incucyte analysis to determine cell doubling time and seeding density for cytotoxicity study using Stem Cells Engineering, Polymer Synthesis/processing; Perform assays in cell-based format suitable for SAR screening in 96 and 386-well formats; Support cell banking and maintain cell line inventory; Execute validated assays for compound screening. | 4/24/2024 |
| 2934 | WuXi Apptec San Diego, CA Research Associate II - In Vivo Pharmacology Master degree in Molecular and Cell Biology or Bachelor degree. Exp: MS: 0 years; BS: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 4/24/2024 |
| 2935 | WuXi Apptec San Diego, CA Research Associate II (Temp/Contingent) Master degree in Molecular and Cell Biology or Bachelor degree. Exp: MS: 0 years; BS: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate III to support our in vivo pharmacology team for various projects. | 4/24/2024 |
| 2936 | WuXi Apptec Philadelphia, PA Laboratory Technician I Associates’/Bachelor’s (science preferred) degree. Exp: 0-2 years |
The Laboratory Technician I performs cell culture and cell-biology based assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under direct supervision, completes batch records and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs additional Research & Development activities as required. | 4/24/2024 |
| 2937 | WuXi Apptec Cranbury, NJ Associate Scientist I (Contingent/Temp) Bachelor’s degree in animal science, biology, or a related discipline. Exp: 0-3 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC standards. Operates lab equipment including oxidizers, centrifuges, LS counters, and cage/tunnel washers. **Please note that this is a contingent/temp position and not eligible for benefits.** Schedule: Monday to Friday 6:30 AM - 3:00 PM (occasional weekend rotations | 4/24/2024 |
| 2938 | WuXi Apptec Philadelphia, PA Bioprocessing Associate I AS/BS Exp: 0+ years |
The Bioprocessing Associate I is responsible for providing support in performance of activities within production facilities to support manufacture of Master and Working Cell Banks Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). The Bioprocessing Associate I is responsible for providing support in performance of activities within production facilities to support manufacture of Master and Working Cell Banks Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 4/24/2024 |
| 2939 | Cel-Sci Baltimore & Elkridge, MD Validation Technician B.S. in science or engineering or a related discipline or 2-year degree. Exp: AS: 1 to 2+ years |
The Validation Technician is responsible for supporting validation activities of GMP equipment and systems. Assists in specifying and selecting equipment. Maintains all records related to qualification and validation. Prepares validation reports, suggests, and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Technician reports to the Validation Engineer. | 4/24/2024 |
| 2940 | Cel-Sci Baltimore & Elkridge, MD Validation Engineer B.S. in a related discipline. Exp: 1 to 5+ year |
The Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor. | 4/24/2024 |
| 2941 | Cogent Professionals Indianapolis, IN Pharma Lab Technician AS degree in chemistry, biology or related science and/or equivalent college coursework in the sciences. Exp: 0+ years |
We currently have a role available for a Pharmaceutical Lab Technician. Job duties include, but are not limited to, the following: General lab organization: order lab gases; put away clean glassware; refill lab solvents; maintain cleanliness and organization of labs, hallways, back-up hoods, waste disposal stations, and storage areas. Chemical preparation: Basic reagent and solvent preparation and transporting to different labs as needed. Instrument care: submit maintenance requests and coordinate with service providers; defrost lyophilizers; check balances for correct operation and appropriate cleanliness; fill liquid nitrogen for NMRs; clear NMR sample carousel; refill LC-MS solvents and QC vials; prepare LC-MS wash solvents; check LC-MS standards; routine preventative maintenance of vacuum pumps. Purification instrument duties: fill solvents and collection racks for flash systems; ensure consumables are properly stocked; dispose of waste solvents and tubes; refill wash bottles; clean and properly store reusable columns. Stockroom support: deliver chemicals from and return items to chemical inventory system; appropriately segregate chemicals; inventory reconciliation; assess safety labeling of compounds to maintain appropriate labels | 4/26/2024 |
| 2942 | Concuir Consulting Los Angeles, CA Project Engineer II/III BS Engineering degree required, Chemical, Mechanical or Biomedical preferred. Exp: 1-4+ years’ |
As a full-time employee of Concuir, Inc, you will provide consulting services to pharmaceutical, biotech and/or medical device manufacturing clients. In this role, you will quickly learn common client practices, recommend and implement improvements to reach project goals, and have the opportunity to scale-up and bring new products into manufacturing. You will be able to utilize your experience as well as benefit from Concuir’s portfolio of project management and cGxP best practices to drive your overall success. Projects range from design through qualification of production equipment, utilities modification, implementation of new facilities and process scale ups. | 4/26/2024 |
| 2943 | Cosette Pharmaceuticals Lincolnton, NC Chemist I - 1st shift and 2nd shift BS or BA in Chemistry or related science. Exp: 0+ years |
Basic Purpose: Provide technical support to plant operations Essential Functions and Responsibilities: Basic wet chemical and instrumental testing of raw materials, in-process, finished product, and stability samples Basic maintenance of instrumentation and equipment in support of laboratory testing Inventory control and maintenance of laboratory chemicals and supplies Adherence to policies of EHS Other duties as assigned by management | 4/26/2024 |
| 2944 | Cytokinetics South San Francisco, CA Research Associate I B.S. in scientific discipline. Exp: 0-2 years |
We are currently in search of a highly motivated Research Associate who possesses a strong passion for the field of Medicinal Chemistry, to become an integral part of our dynamic team. The ideal candidate will bring forth their expertise and enthusiasm to actively contribute to and enhance our ongoing efforts and initiatives in the realm of pharmaceutical research and development. | 4/26/2024 |
| 2945 | Cytokinetics South San Francisco, CA Contract - Research Associate (DMPK) Bachelor's or Master's degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or a related field. Exp: 1+ years |
We are seeking a highly motivated Junior Research Associate with a focus on Drug Metabolism and Pharmacokinetics (DMPK) to join our team. The ideal candidate will contribute to our efforts in screening, plasma protein binding, and microsomal assays. This role offers an exciting opportunity to work in a collaborative and fast-paced environment, supporting the development of cutting-edge therapies for cardiovascular and skeletal muscle disorders. | 4/26/2024 |
| 2946 | Dewpoint Therapeutics Boston, MA Research Associate II - Compound Management M.Sc. or higher in Science, Chemistry, Engineering, or a related field. Exp: 1 year |
We are looking for a creative, energetic individual to join our Lead Discovery and Lead Evaluation team, working directly on compound management and lab informatics. If you’re looking to jump start your career as a Researcher while gaining experience and knowledge in a collaborative and empowering environment, this is the ideal role for you. As the ideal candidate, you will bring experience in managing inventories of both small molecules and biological materials and have a desire to build a career in an industry-leading & cutting edge HTS team. In this position you’ll be part of an energizing and supportive startup culture engaged in continuous learning, and part of an exceptional international team. This role is based at our site in Boston's Seaport district. Dewpoint offers competitive salary, great benefits, and amazing perks. | 4/26/2024 |
| 2947 | Dicerna Pharmaceuticals West Lebanon, NH Quality Control Coordinator Associate’s degree or equivalent. Exp: one (1) or more years |
This position is responsible for coordinating/supporting/assisting the Quality Control team including offsite and onsite calibrations, quality system interaction, management of sample collection and drop-off, communication of production schedule and ad-hoc testing requests, troubleshooting, performing a variety of highly diverse and complex administrative tasks and activities requiring sound planning, organization, judgement, adaptability, and accountability. This position is located in West Lebanon, New Hampshire and will require onsite work and collaboration. It is a full time (40 hour per week) position and the standard schedule is Monday-Friday (8am-5-pm). We offer a competitive salary, commensurate with experience. | 4/26/2024 |
| 2948 | Dicerna Pharmaceuticals West Lebanon, NH Manufacturing Technician Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 4/26/2024 |
| 2949 | Elicio Therapeutics Boston, MA Scientist I/II, Translational Medicine MS. Exp: 0-3 years |
Reporting to the Senior Scientist I of Translational Medicine, this individual will serve as an integral team member with exposure to multiple facets of business operations. The Scientist I will be responsible for conducting immunogenicity assays that measure vaccine efficacy, such as ELISpot/Fluorospot, ICS, and other flow cytometry-based assays. As part of the organization's Translational Medicine team, this individual will interact collaboratively with the Clinical Operations and Analytical Chemistry departments to successfully progress current and future clinical programs. Additional attributes of the position include responsibility for performing in vivo mouse experiments to characterize the immune response to vaccine candidates. Elicio (ELTX) is a growing organization based out of the Seaport area of Boston, Massachusetts with additional staff functioning in a virtual-based environment from the Greater Boston area and throughout the United States. | 4/26/2024 |
| 2950 | BostonGene Waltham, MA Biospecimen Inventory Technician Minimum BS in a Biological or Life Science. Exp: one year |
The candidate will report to the Lab Manager and under their supervision support BostonGenes laboratory teams with sample management and tracking systems/protocols. The candidate will create and oversee a new sample inventory tracking system using the existing Lab Information Management System (LIMS) and Benchling software. Once created they will assist in the transition to an end-to-end barcoding-based system for sample tracking and continuously update and improve the process as new tests are added. This candidate will also be responsible for handling and processing blood specimens for specific projects. This will involve basic blood processing techniques such as blood fractionation, plasma clarification, and cell isolation for downstream biobanking. | 4/16/2024 |
| 2951 | BPS Bioscience San Diego, CA Research Associate I, Molecular & Cellular Biology Bachelor's. Exp: Entry-level |
The position requires the ability to perform and somewhat independently interpret molecular cloning and protein expression experiments. The successful candidate will be tasked with duties in molecular biology, cell culture and transfection techniques. These include standard cloning, PCR techniques, and plasmid preparation and analysis. Expression systems of focus will be mammalian cells (293). This position will include assisting other researchers with their experiments and with lab maintenance. | 4/16/2024 |
| 2952 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required. Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 4/16/2024 |
| 2953 | Cabaletta Bio Philadelphia, PA Research Associate/Sr. Research Associate, Molecular Biology B.S degree in Life Sciences or closely related discipline. Exp: 0-2 years |
Reporting to the Associate Scientist, Molecular Biology group, we are seeking an experienced and motivated Research Associate or Senior Research Associate. Under scientific and technical supervision, the candidate will design and execute cell-based assay advancing multiple discovery programs. The position offers growth into additional areas such as cell biology and molecular biology, immunology, and cell therapy. The position involves both technical and operational responsibilities. | 4/16/2024 |
| 2954 | Caraway Therapeutics Rahway, NJ Specialist, Process Engineering Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Sterile GMP Clinical Manufacturing facility. As the facility is nearing the completion of its construction, the selected candidate will contribute to equipment and facility commissioning/qualification, regulatory certification, as well as other workstreams’ critical activities to enable facility startup and operational readiness. To support these business-critical activities, night and weekend work may be required. Once the facility is operational, this role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of sterile clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 4/16/2024 |
| 2955 | Caraway Therapeutics Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related field. Master’s degree in Chemical Engineering, Chemistry, Ph Exp: BS: 1 year |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 4/16/2024 |
| 2956 | Bayer Luling , LA Chem Production Engineer Bachelor’s of Science degree in Chemical Engineering, including May 2024 B.S. Chemical Engineering graduates. Exp: 0-3 years |
The Chemical Production Engineer provides support to plan, coordinate, and execute technical activities needed to support manufacturing operations. Also, ensures the safe, efficient, productive, and environmentally sound manufacture of active ingredients or intermediates. | 4/17/2024 |
| 2957 | Bayer Berkeley, CA Associate Electrical Engineer M.S. Degree in Electrical Engineering or related discipline. Exp: 0-1 years |
Exciting and challenging electrical engineering opportunity where each day is different. Tasks would include evaluating electrical capacity, emergency power readiness, equipment maintenance, alternative sustainable energy solutions, and component electrical ratings analysis. Interact with cross-functions including Quality, Production, Procurement, Investment Management, Research and Development at the at the local, regional, and global levels as well as external vendors, and CA state supplier. | 4/17/2024 |
| 2958 | Bayer Huxley, IA Agronomic Research Specialist II (Field) - Huxley, IA Bachelor’s degree completed by start date. Bachelor’s or Master’s degree in agronomy, life sciences, engineering. Exp: 1+ years |
As a field-facing Agronomic Research Specialist II, you will be responsible for contributing to an R&D Field Trial program for corn and soybeans. Your primary responsibilities will be to coordinate with growers on leased land space and assist with acquiring and supervising local staffing during in-season activities. You will conduct in-season research activities such as phenotyping, study management, and data analytics review as part of overseeing and executing research trials that feeds the R&D pipeline. Additionally, you will have the opportunity to partner with other Agronomic Research Specialists on site, as well as other cross-site functions on initiatives to improve data quality, standard operating procedures, or quality/compliance actions. This is an onsite role (site and surrounding production fields), primarily day shift (with extended hours during peak season) at our Huxley, IA research facility.As a field-facing Agronomic Research Specialist II, you will be responsible for contributing to an R&D Field Trial program for corn and soybeans. Your primary responsibilities will be to coordinate with growers on leased land space and assist with acquiring and supervising local staffing during in-season activities. You will conduct in-season research activities such as phenotyping, study management, and data analytics review as part of overseeing and executing research trials that feeds the R&D pipeline. Additionally, you will have the opportunity to partner with other Agronomic Research Specialists on site, as well as other cross-site functions on initiatives to improve data quality, standard operating procedures, or quality/compliance actions. This is an onsite role (site and surrounding production fields), primarily day shift (with extended hours during peak season) at our Huxley, IA research facility. | 4/17/2024 |
| 2959 | AstraZeneca Frederick, MD Production Technician I - Night Shift BS/BA degree preferred. Degree in STEM field. Exp: 1+ years |
In this role, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also train with a qualified Technician on activities related to operating process equipment with the requirement of qualification. Additionally, you will follow and execute cGMP documentation, utilize Manufacturing Execution systems (MES), contribute to problem-solving activities for non-routine activities on the production floor, and participate in continuous improvement activities for Manufacturing. Adherence to AstraZeneca values and behaviors is expected. | 4/17/2024 |
| 2960 | AstraZeneca Frederick, MD Production Technician I/II - Nights BS/BA degree preferred. Degree in STEM field. Exp: 0-1 years |
Your responsibilities will include operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. You will be expected to demonstrate advanced equipment/process knowledge to diagnose issues and participate in first-line troubleshooting and root cause analysis. You will also be responsible for maintaining qualifications in Production Technician duties, executing work orders within the system, and leading continuous improvement initiatives. | 4/17/2024 |
| 2961 | AstraZeneca Frederick, MD Production Technician II-Night Shift BS/BA degree preferred. Degree in STEM field. Exp: 0-1 years |
As a Production Technician, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also be a qualified trainer on-the-floor, follow and execute cGMP documentation, maintain qualifications in Production Technician duties, and utilize Manufacturing Execution Systems (MES). Furthermore, you will contribute to problem-solving activities and troubleshooting for non-routine activities on the production floor. You will lead indirect processing activities in support of MFG operations and continuous improvement initiatives. Adherence to AstraZeneca values and behaviors is a must. | 4/17/2024 |
| 2962 | Bachem Vista, CA Process Engineer Bachelor’s degree in mechanical, electrical, chemical, manufacturing engineering or science related field. Exp: 1-3 years |
The process engineer is responsible for supporting and maintaining critical and supporting equipment and instruments to ensure the manufacturing process is continuously in operation with minimal downtime. Concurrently, through process mapping, the process engineer is responsible to develop process improvement projects to create efficiency in the process. The process engineer will also be responsible for identifying and researching background for equipment purchases and making recommendation to management. | 4/18/2024 |
| 2963 | Covance Burlington, NC Molecular Diagnostic Specialist for DNA Identification Bachelor's Degree in Biology, Chemistry or Life Science. Exp: 1 year |
The DNA Identification Building in Burlington, NC is seeking a Molecular Diagnostic Specialist. The Molecular Diagnostic Specialist helps to support the operations team, the quality team and the laboratory in various ways while also maintaining the laboratory equipment and their records. As a Molecular Diagnostic Specialist, this role will help support the development and optimization of new and existing molecular diagnostic tests. Conducts routine to complex experimental procedures within overall scope of a research project and/or diagnostic test development project. Maintains all appropriate records regarding data collection and interpretation of results. Daily activities include scripting for automation, validation of equipment and consumables, general instrument repairs, and monitoring PMs. The MDS team is vital in constant lab streamlining and preventing down time in lab processing. LabCorp's Consumer Genetics operation is one of the world's largest genotyping facilities, having genotyped millions of samples for SNP (Single Nucleotide Polymorphism) analysis since 2013. SNPs are single base changes in DNA that give rise to genetic variation. These variations can be used for ancestry typing, health and disease risk factors, carrier conditions, and curiosity testing! The working schedule for this position will be: Monday - Friday 2 pm - 10:30 pm, 10% shift differential offered for 2nd shift. | 4/18/2024 |
| 2964 | Covance Burlington, NC Technologist for Moleclar Micro Bachelor's degree in Biology, Chemistry, Medical Technology or a related science. Exp: 1 year |
Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our lab team as a Technologist in Burlington, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives." This position is also responsible for supporting the COV2 team to include duties such as assay building and releasing results. The schedule for this position will be: 2nd shift, Tuesday-Sat, 2:00pm-10:30pm. Eligible for 10% shift differential due to 2nd shift hours. | 4/18/2024 |
| 2965 | Covance Raritan, NJ Clinical Laboratory Technologist - Molecular Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 1 year |
Are you an experienced clinical laboratory professional looking for leadership opportunity? Are you detail oriented, process focused, and enjoy leading others? Are you looking for an industry leading company that offers growth and stability? LabCorp is seeking a Clinical Laboratory Technologist to join our Core Laboratory team in Raritan, NJ. In this position, you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". Work Schedule: Tuesday - Saturday: 3:00 pm - 11:30 pm | 4/18/2024 |
| 2966 | Covance Raritan, NJ Clinical Laboratory Technologist - Chemistry Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 0+ years |
Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team in Raritan NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Work Schedule: Work Schedule: Tuesday - Saturday (12:00am - 8:30am) and alternating Saturdays (11:30pm- 8:00am) New Grads Welcome – Full Training Provided | 4/18/2024 |
| 2967 | Covance Raritan, NJ Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! Pay Based on Experience -- Starting @ 28.50/hour Sign-On Bonus of $5,000 ( External Candidates Only ) The work schedule for this position will be Sunday - Thursday 10:00 pm - 6:30 amAre you an experienced Medical Lab Professional? | 4/18/2024 |
| 2968 | Covance Raritan, NJ Clinical Laboratory Technologist - Forensics Toxicology Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet localregulatory (CLIA & State) requirem Exp: 0+ years |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. New Grads Welcome - Full Training Required Work Schedule: Tuesday – Saturday - 7:00 am - 3:30 pm | 4/18/2024 |
| 2969 | Covance Holyoke, MA Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Holyoke, MA. In this position, you will work in a fast-paced, customer-focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! The work schedule for this position will be Tuesday - Saturday 10:00 pm - 6:30 am | 4/18/2024 |
| 2970 | Dexcom San Diego, CA Mechanical Engineer II Master’s degree in a technical discipline. Exp: 0-2 years’ |
The R&D Mechanical Engineering Characterization Team is responsible for the feasibility and development of next-generation products at Dexcom. We’re seeking a cross-functionally disciplined engineer with subject matter expertise across mechanics, materials, and human tissue/device interaction to support characterization and test of novel patch materials and designs. Positioned within the Mechanical Engineering team, this is a high visibility, high impact role in achieving Dexcom’s product performance and reliability goals through delivering functional excellence in the research, development, and characterization of technologies/designs & their integration to a product ecosystem. | 4/18/2024 |
| 2971 | Emergent BioSolutions Baltimore, MD Analyst II, Quality Assurance - 3rd-Shift BS or BA degree in Science or Engineering. Exp: 0-2 years |
The Analyst II on the Floor is responsible for assuring the quality of products manufactured at the Emergent BioSolutions Baltimore Facility. The Analyst II will perform Quality on the Floor functions. Our QA Department provides expertise in problem-solving and process improvements. The QA Specialist will interact with manufacturing personnel and Quality Engineers to provide guidance necessary to maintain and improve CGMP compliance at the company. | 4/18/2024 |
| 2972 | Emergent BioSolutions Baltimore, MD Analyst II, QA on the Floor BS or BA degree in Science or Engineering. Exp: 0-2 years |
This role is responsible for monitoring Warehouse areas, Printed Material inventory management,Packaging Operations support, and Warehouse Quality on the Floor continuous improvement. | 4/18/2024 |
| 2973 | Emergent BioSolutions Baltimore, MD Analyst II, QC Microbiology, 3rd Shift (Wed-Sat) MS in Microbiology/Biology or related field. Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Emergent BioSolutions Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. This is a 3rd-shift/4 day work week position -working hours 10pm-8:30am-Wednesday through Saturday. Hours may vary to meet business and training needs. | 4/18/2024 |
| 2974 | Emergent BioSolutions Winnepeg, MB, CA Analyst I, QC Laboratory Services - Limited Term University degree or technical diploma in microbiology, biology or related field of study. Exp: 0-2 years |
The Analyst I, QC Laboratory Services performs GMP compliant microbiological testing as required to support Raw Material testing, In-process, Finished Product release & Stability or nonclinical/ clinical studies. The Analyst I may also perform testing required to support assay and process validations. He/She will perform testing to support release of lab specific material (media, standards). | 4/18/2024 |
| 2975 | Emergent BioSolutions Rockville, MD Sr Bioprocess Associate BS/BA in Biology, Chemistry, or related discipline. Exp: 1-3 years’ |
The primary role of this position is to provide technical support for all fill finish operations with strict adherence to cGMP compliance. The candidate will also provide guidance for all on-floor activities including aseptic fill operations, visual inspection, labeling, and packaging of bulk product with minimal supervision. This position requires proficiency in aseptic technique, and deliberate movements inside various isolators. The candidate for this position will be working in close association with Technical Operations, Quality Assurance, Quality Control, and Material Management to overcome challenges in meeting the production schedule. | 4/18/2024 |
| 2976 | Leidos Biomedical Research San Antonio, TX Research Associate Master’s degree or equivalent. Degree should be in a related field. Knowledge of animal anatomy and physiology. Exp: 1+ years |
Are you ready for an opportunity to make a difference in the lives of those who serve our country? Leidos Health Solutions is currently looking for a Research Associate with molecular biology experience to support the Directed Energy (DE) department at the Naval Medical Research Unit, San Antonio (NAMRU-SA) in San Antonio, TX. NAMRU-SA conducts gap driven combat casualty care, craniofacial, and directed energy research to improve survival, operational readiness, and safety of Department of Defense personnel engaged in routine and expeditionary operation. | 4/19/2024 |
| 2977 | Leidos Biomedical Research Dayton , OH Electrical Engineer Bachelor’s degree in an engineering discipline (electrical, computer, or similar). Master’s degree or higher in electrical or computer engineering. Exp: BS: 0-3 years |
Leidos is searching for an Electrical Engineer to support AFRL’s Dynamic Infrared Missile Evaluation (DIME) Laboratory located on Wright Patterson Air Force Base, OH. The successful candidate will utilize a strong engineering background designing, testing, modeling, simulating, and analyzing the next generation of infrared countermeasure techniques. This position will support multiple simultaneous research efforts within the laboratory requiring skills including hands-on experimentation, digital modeling using graphical programming, modeling and simulation of aircraft/missile engagements, and computer application development involving interfacing with hardware systems and real-time processing. Addressing our customers’ challenging mission requirements necessitates research and development of new capabilities as well as making improvements to existing systems. The successful candidate will be required to quickly develop an understanding of legacy efforts and engineer improvements to meet new requirements. Additionally, the engineer will be called upon to develop new and innovative solutions to challenging problems, helping our customers provide solutions for the warfighter. The successful candidate will work as part of an integrated team but should also be proficient at conducting independent research. | 4/19/2024 |
| 2978 | Leidos Biomedical Research Huntsville, AL Entry-Level Firmware Engineer Bachelor of Science in Electrical Engineering or equivalent degree from an ABET-accredited institution with a 3.0 or higher GPA. Exp: 1+ years |
Primary Responsibilities In this role, project assignments could be focused in one or multiple of the following areas: Design, simulation, and testing of firmware using hardware description languages (HDL) to drive custom hardware. Testing and integration of RF electronics such as high speed DACs used for waveform generation and ADCs used for signal processing. Utilizing cutting edge AMD/Xilinx FPGA and SoC families and design tools such as the RFSoC. Testing and debugging hardware using lab equipment such as spectrum analyzers and oscilloscopes. Working on multidisciplinary teams to debug problems when integrating firmware and PCB designs with Radar and Seeker hardware. | 4/19/2024 |
| 2979 | Leidos Biomedical Research Huntsville, AL Penetration Tester- Entry Level Master’s degree in Cyber Security, Computer Science, Computer Engineering, Electrical Engineering. Exp: 1+ years |
Leidos Defense Systems is seeking a full-time, talented, and motivated Penetration Tester to perform penetration tests on customer systems in the defense, space, cyber, and commercial fields. The ideal candidate will possess technical skills in networking, operating systems, and programming, as well as the ability to think creatively about potential threats. They will also possess the ability to analyze both open and closed-source intelligence to determine potential cyber threat Tactics, Techniques, and Procedures (TTPS), attack vectors, and risks to systems of various size and complexity. | 4/19/2024 |
| 2980 | Leidos Biomedical Research Patuxent River, MD Junior Network and Computer Systems Administrator (ROD) Bachelor’s Degree in Computer Science, Mathematics, or Engineering from an accredited college or university. Exp: 1+ years |
The Leidos Defense Group is seeking an entry level Network and Computer Systems Administrator to provide networking support as part of the Range Operations Division (ROD) Range Support Branch of the Atlantic Test Range (ATR) in Patuxent River, Maryland. Members of this dynamic team design and develop complex hardware and software network architectures to support real-time Research, Development, Test, & Engineering (RDT&E) test and fleet training events conducted by ATR in support of customers’ requirements. | 4/19/2024 |
| 2981 | Eli Lilly Indianapolis, IN Biologist - In Vivo Neuroscience BS/MS in Biology, Animal Sciences, Pharmacology, or a related field. Exp: 1+ years |
Lilly Neuroscience is seeking an experienced scientist (Bachelors or Masters) to join the Neurodegeneration team to facilitate its mission of discovering novel medicines for the treatment of Alzheimer’s disease, Parkinson’s disease, ALS, and other related neurodegenerative conditions. The individual will join a laboratory focused on in vivo research to support our expanding neurodegeneration portfolio, and they will leverage their technical expertise to lead high quality studies and sample collection to support identification/development of novel targets for Neurodegenerative conditions. A key focus of the scientist will be the utilization of multiple in vivo techniques including complex surgical models to support therapeutic investigations in pre-clinical animal models. Importantly, the individual will collaborate with colleagues across the Neurodegeneration group to facilitate both exploratory and portfolio workstreams. The scientist must possess a strong work ethic and an ability to quickly master numerous new techniques. Lilly has a proud record of drug development for neurodegenerative diseases that has been driven by a highly collaborative and diverse team of accomplished scientists. | 4/19/2024 |
| 2982 | Eli Lilly Indianapolis, IN Associate Biologist BS or MS in biology/animal science/veterinary technology or a closely related field. Exp: 1 year |
The Lilly Diabetes, Obesity and Complications Therapeutic Area (DOCTA) is focused on discovery and development of new therapeutics for the treatment of medical complications arising from type 2 diabetes and obesity. The cardiorenal team is looking for a biologist to conduct experiments using animal models of renal and metabolic diseases. The ideal candidate should be goal-oriented and dedicated, capable of conducting thorough research studies with minimal oversight. This biologist will design and perform experiments independently and within team-based environments, as well as interact with internal and external collaborators. Are you ready to actively engage in cardiorenal drug hunting teams and serve as a scientific and technical advisor to project teams? Apply now to join the Lilly Team! | 4/19/2024 |
| 2983 | Eli Lilly Boston, MA Associate Scientist, Early Preclinical Development - Inner Ear Biology Bachelor's Degree. Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 4/19/2024 |
| 2984 | Eli Lilly Cambridge, MA Scientist - In Vivo Surgical Associate Bachelors or Masters degree in neuroscience or related fields preferred. Exp: 1+ years |
The Next Generation Therapeutics group is a newly formed team with a focus on using novel therapeutic modalities to deliver medicines for chronic pain and neurodegenerative disorders. The group, based at our Cambridge Innovation Center in Kendall square, will work with internal and external partners to identify, and deliver new novel therapies into patients at speed. The team is seeking experienced and inspiring scientists to join our fast-paced, interdisciplinary team as we leverage innovative RNA/oligonucleotide/gene and genomic based therapeutics to enhance our portfolio. | 4/19/2024 |
| 2985 | Eli Lilly Lebanon, IN Manufacturing Scientist - Lebanon API Manufacturing Master's Degree in STEM Discipline (Chemistry preferred). Exp: 1 year |
The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 4/19/2024 |
| 2986 | Eli Lilly Lebanon, IN Associate- Laboratory Support - Quality Control - Advanced Therapies Bachelors (4-year) degree in a science field related to chemistry, microbiology, biology, or other science discipline. Exp: 1+ years |
The Laboratory Support Associate is a support role in the Quality Control Laboratory helping to ensure proper and efficient functioning of laboratory operations. The Laboratory Support Associate is responsible for operational excellence and continuous improvement in the laboratory. They will manage laboratory samples, materials, reagents, equipment usage, ordering, organization, and may include management of laboratory system access. | 4/19/2024 |
| 2987 | Eli Lilly Lebanon, IN Process Engineer - API Manufacturing Bachelor's Degree in Chemical, Biochemical, Bioprocess, Process, or Mechanical Engineering. Exp: 1+ years |
We are seeking Process Engineers to support the API Manufacturing Business in Lebanon. Process Engineering is core to delivering our product pipeline across batch and continuous API production and development. | 4/19/2024 |
| 2988 | Meridian Medical Technologies Cambridge, MA Associate Scientist, Protein Production & Engineering, BioMedicine Design Bachelor’s degree is required with a Life Science major. Exp: 0 to 3 years |
Pfizer’s BioMedicine Design (BMD) is seeking a highly motivated Cell and Molecular Biologist to join Biotherapeutics Expression and Purification group (BEP) located in Pfizer Worldwide Biotherapeutics Research campus of Cambridge MA. Qualified candidate will play an essential role in support of large-scale non-GMP transient protein lead production across Pfizer’s diverse biotherapeutics discovery portfolio to enable Pfizer’s research units and their pre-clinical therapeutics in-vitro and in-vivo needs. This individual will work in the area of therapeutic protein production and engineering in mammalian cells. The individual will perform mammalian cell culture, molecular biology, large-scale mammalian cell expression, and protein production analysis for supporting protein therapeutics discovery efforts. The individual will perform this function with supervision, toward considerable independence, and will display initiative in learning new techniques. The candidate will contribute to the group wide deliverables and be required to work on several projects simultaneously presenting results and updates at group meetings. | 4/19/2024 |
| 2989 | Meridian Medical Technologies Andover, MA Associate Scientist, Cell Line Development B.S in cellular/molecular biology or related life science field. Exp: 0-3 years |
A technical, lab-based position is available within Pfizer’s Molecular and Cellular Technologies organization. The position will be primarily involved in mammalian cell line development (CLD) portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer’s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. The successful candidate will possess excellent aseptic technique and have experience with mammalian cell culture and recombinant protein expression. | 4/19/2024 |
| 2990 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex Assays. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 3/27/2024 |
| 2991 | Advanced Cell Diagnostics Minneapolis, MN Advanced Quality Technician An associate degree. Exp: 0+ years |
The responsibilities of an Advanced Quality Technician are to perform tasks in the process of inspecting and testing science products. Duties may require interpreting results, inventory, and participation in complaint investigations. This position will participate in the continuous improvement of our products and customer-centered culture. | 3/27/2024 |
| 2992 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate MS degree in the biological sciences. Exp: 0-2 years |
As an Advanced Research Associate you will work in the Immunocytochemistry Department on the validation of antibodies for immunocytochemistry applications. You will be knowledgeable of animal anatomy and histology and familiar with histological examination of tissues, frozen and paraffin-embedded tissue sections, immunohistochemistry protocols, microscopy systems; collect digital images, digital image post-processing and enter data into a database. | 3/27/2024 |
| 2993 | Advanced Cell Diagnostics Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 year |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 3/27/2024 |
| 2994 | Advanced Cell Diagnostics Newark, CA Senior Research Associate, PAS MS in molecular biology, biochemistry, cell biology or related field. Exp: 0-2 years |
The Senior Research Associate (SRA) will serve as a key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic sponsors to detect RNA targets of interest. An additional critical work component will be the application of immunohistochemistry (IHC) to look for specific protein targets. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. It is expected that the Sr. Research Associate will independently collect and interpret data based on project expectations, which has implications for many downstream applications, such as biomarker validation and cell and gene therapy. The SRA will also be expected to independently utilize available resources for any required troubleshooting and communicate clearly with sponsors through both electronic mail and teleconference channels. The SRA must also coordinate with internal research and development (R&D) team to learn new techniques quickly and be able to adapt to shifting priorities in a fast- paced and growing start-up environment. | 3/27/2024 |
| 2995 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of methylcellulose, methylcellulose-containing media, and stem cell and gene therapy (SCGT) media. Perform QC testing and analysis of some methylcellulose-containing media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Perform additional duties as assigned. Skills used include cell culture, high attention to detail, strong communication and organizational skills. | 3/27/2024 |
| 2996 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree in a related field. Exp: up to 3 years |
Are you passionate about science, an adaptable self-starter with an insatiable curiosity and have a drive to innovate and further develop your skills with a multitude of analytical tools to study and characterize biomolecules? As a Research Associate in the Analytical Services team, you will be responsible for performing routine Quality Control (QC) testing, and participating in troubleshooting efforts for released products and new products that are still in development through the application of biophysical analysis of proteins and antibodies focusing on our capillary electrophoresis systems, but may also include chromatography, immunoassays, light scattering and other analytical tools, with the aid of fully defined SOPs. You will also actively take part in group projects, participate in process improvement efforts to improve lab protocols with the goal of facilitating innovation, efficiency and productivity, and perform additional duties as assigned. | 3/27/2024 |
| 2997 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Associate I - Mid-Shift Bachelors in a science or engineering discipline preferred. Exp: zero to two (2) years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 3/27/2024 |
| 2998 | Akcea Therapeutics Carlsbad, CA Research Associate II/ Senior Research Associate, Core Antisense Research Master’s degree preferred in biochemistry, molecular biology or cell biology, or a B.S. Exp: MS: 0+ years; BS: >1-2 years |
We are seeking a highly qualified and motivated individual to perform basic research to increase our understand on how ASOs target RNA to modulate the expression of genes. The position offers the opportunity to do groundbreaking science and make discoveries that will create the next generation of ASO medicines. The selected candidate will become an integral part of an interdisciplinary and energetic team of scientists in the Ionis Core Research group. | 3/27/2024 |
| 2999 | Akouos Indianapolis, IN Analytical Chemist - Bioproduct Research & Development MS in Analytical Chemistry, Biochemistry, Chemistry, or a related field. Exp: 0+ years |
The Bioproduct Research and Development (BR&D) organization delivers new medicines to patients through the development and commercialization of insulins, peptides, oligonucleotides, monoclonal antibodies, novel therapeutic proteins, and gene therapy systems. BR&D is a multidisciplinary group with deep technical expertise that works collaboratively with our discovery and manufacturing colleagues. Located in Indianapolis, IN, scientists have full access to Lilly’s deep pharmaceutical development expertise and engineering capabilities. In this role, you will be part of a diverse team of analytical chemists, pharmaceutical scientists, and engineers delivering product and process understanding across a broad range of platforms. Ideal candidates will possess experience across multiple analytical techniques, demonstrate an aptitude in technical problem solving, and be motivated to work both independently and collaboratively in a dynamic environment. | 3/27/2024 |
| 3000 | Akouos San Francisco, CA Research Associate - DMPK BS or MS in chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based Research Associate to join our Drug Metabolism and Pharmacokinetics (DMPK) team. This individual will be a key contributor to performing standard ADME/DMPK assays, such as microsomal stability, plasma protein binding, and metabolite identification. The individual will also be responsible for operating LC-MS instruments (QQQ and HRMS) with minimal direction. Do you have experience in mass spectrometry while doing enzyme related work? This role may be perfect for you! | 3/27/2024 |
| 3001 | Akouos Boston, MA Associate Scientist, Early Preclinical Development - Inner Ear Biology Bachelor's Degree. Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 3/27/2024 |
| 3002 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Downstream Process Development MS degree in Biochemistry, Chemistry, Chemical Engineering or related discipline from an accredited university. Exp: 0+ years |
The Associate Scientist II is responsible for performing assigned experimental tasks to support the development and optimization of manufacturing processes for Alexion’s biotherapeutic candidates. The Associate Scientist II will work routinely in collaboration with other members of Biologics Process Development, Technology Transfer and Analytical Sciences, including all other groups in Product Development and Clinical Supply. | 3/27/2024 |
| 3003 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Pilot Plant Operations MS. Exp: 1+ years |
The Associate Scientist II will perform assigned tasks to support the operational scale up of Pilot-scale manufacturing processes for Alexion’s bio-therapeutic candidates. Work routinely in collaboration with other members of Process Development and other groups in Product Development and Clinical Supply organization. | 3/27/2024 |
| 3004 | Ampac Analytical Rancho Cordova, CA Automation Engineer II Master's Degree in Engineering or Computer Science. Exp: 0-2 years |
Mid-level Automation Engineer will be responsible for PLC Programming, Citect HMI Development, and cGMP documentation development and execution. Additional responsibilities will include developing, testing, and maintaining custom software applications to solve unique problems in a manufacturing environment. Execute small internal control system projects, manage larger vendor supported control system projects. Coordinate and advise process engineering on control system requirements. Engineer must be able to perform industrial field work which may involve some lifting, use of ladders, and stairs. Works under general supervision. | 3/28/2024 |
| 3005 | Ardelyx Fremont, CA QA Specialist III (CSV) Bachelor’s degree in a technical discipline, science /engineering discipline preferred but not required equivalent experience may be considered. Exp: 1-7 years |
We are seeking a highly skilled and detail-oriented QA Computer System Specialist to join our team. The ideal candidate will be responsible for overseeing the quality assurance for all GxP computer systems within our organization. The person in this role will work with the functional teams to ensure that all GxP regulated systems are purchased, audited, installed and maintained according to industry best practices (e.g. GAMP5) and regulatory requirements (e.g. 21CFR Part 11 and relevant FDA Guidance). The position will also support plan and organize QA activities for computer system validation projects. Specific duties of this role include, but are not limited to, overseeing and approving validation- related documents, conducting risk assessments, determining which elements of projects should be validated, assessing and/or coordinating impact of proposed changes to computerized systems, and support activities to prepare for inspections (both external and internal) related to computer system validation. The candidate will also be responsible for maintaining GxP computer systems in a validated state in addition to support designing work processes for users and administrators of these systems. In addition, this position will involve interacting with regulatory agencies and corporate partners during inspections and audits and may require travel to audit computerized system vendors off-site. The incumbent will also develop and implement strategies to ensure compliance with CSV requirements and consistent application of relevant policies and processes. | 3/29/2024 |
| 3006 | Arrowhead Pharmaceuticals Verona, WI Associate Manufacturing Scientist I (2nd shift) BS or MS in chemistry, biochemistry, engineering, or related scientific field. Exp: Entry level to 3 years |
The Associate Manufacturing Scientist I (second shift) supports the production of drug substances and drug products. Their responsibility will focus on the preparation of solutions and reagents by following standard protocols. This technically focused second shift position supports lab work, helps solve problems, and effectively communicates with colleagues. | 3/29/2024 |
| 3007 | Arrowhead Pharmaceuticals Verona, WI Associate Scientist, CMC Process Development BS or MS in chemistry or biochemistry with an excellent understanding of organic and analytical chemistry. Exp: 1+ years |
Chemist in the Development Chemistry Group focusing on oligonucleotide synthesis development. This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates. | 3/29/2024 |
| 3008 | Atec Spine Carlsbad, CA Quality Engineer Minimum Bachelor’s degree (BS) from a four-Year College or university in Mechanical, Industrial and Systems, Biomedical, or Manufacturing Engineering. Exp: 1-5 years |
Develop and improve, with an emphasis on implementation, inspection methods, gages, process control techniques, standard operating procedures, inspection plans, test protocols and test reports to ensure safety, reliability and efficacy of new products and processes. | 3/29/2024 |
| 3009 | Atec Spine Carlsbad, CA Validation Engineer Bachelor’s degree from four-year College or university in Engineering, or equivalent experience. Exp: 0-3 years |
Validation Engineering for New Product Development & Sustaining Engineering with a focus on software systems. Under minimal supervision, the Validation Engineer will work closely with QE, R&D, Marketing, Product Development teams, Supply Chain, and Regulatory to bring products to market while ensuring compliance to applicable standards and regulations. | 3/29/2024 |
| 3010 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters in science related field. Exp: 0-1 year |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 3/29/2024 |
| 3011 | Beam Therapeutics Durham, NC Manufacturing Associate (Multiple Openings) BS, MS a plus, in Life Sciences or Engineering. Exp: 0-5 years |
Beam is expanding our geographical footprint to RTP, NC with the recent announcement of a 100,000 square foot manufacturing facility in addition to our laboratory-based facilities located in Cambridge, MA. We are looking for highly energetic Manufacturing Associates to support start-up and scaling of cGMP manufacturing at our new RTP site. The successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and start-up. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment. | 3/29/2024 |
| 3012 | Beam Therapeutics Durham, NC QC Analyst Bachelor’s degree required, preferably in a chemistry, life science, or related discipline. Exp: 1-3 years |
Beam is seeking a highly motivated and energetic Analyst to join our growing QC analytical team. The Quality Control Analyst will be responsible for performing various analytical methods to evaluate the quality of critical in-process samples to support cGMP manufacturing operations across multiple site programs. This role will also be responsible for daily laboratory operations including reagent receipt and inventory management and equipment maintenance. This position will support deviation initiation and investigations as well as implementation of continuous improvements. The Analyst will support critical analytical method implementation workstreams in support of program start-up and scale up. This role will work closely with team members in Quality Assurance, Manufacturing, MS&T and Analytical Development. The position will report to the Senior QC Manager. The Analyst I is expected to be an on-site resource at Beam’s manufacturing facility in RTP, North Carolina to support project start-up and routine clinical and commercial operations. | 3/29/2024 |
| 3013 | Berkshire Sterile Manufacturing Lee, MA Formulation Associate I Associates Degree in a science-related discipline. Exp: Zero to two (0-2) years’ |
Perform all formulation operations in the area of assignment and support start-up/changeovers/tech transfer activities. This position works under the immediate direction of the Formulation Supervisor and all work is conducted following a high standard of GMP compliance and written SOP and batch records. | 3/29/2024 |
| 3014 | Berkshire Sterile Manufacturing Lee, MA Manufacturing Associate- 2nd Shift Associates Degree. Exp: zero (0) to two (2) or more years |
Perform all production operations in the areas assigned within the facility. Perform production support operations in areas assigned and support start-up, changeovers and tech transfer activities. | 3/29/2024 |
| 3015 | Berkshire Sterile Manufacturing Lee, MA Process Engineer Process Engineer: Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science. Exp: One (1) to three (3) years |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 3/29/2024 |
| 3016 | Berkshire Sterile Manufacturing Lee, MA Facilities Engineer Bachelors or Master’s engineering degree. Exp: Up to two (2) years |
The Facilities Engineer will supply engineering expertise to support and continually improve mechanical systems at BSM within the requirements of relevant regulations, cGxPs and the BSM Quality Management System. The Facilities Engineer will perform all work under the supervision and direction of the Senior Engineering Manager. | 3/29/2024 |
| 3017 | BioLife Solutions Bothell, WA Aseptic Technician I Bachelor’s degree; or Associate degree / Biotech cert. Exp: 1 year |
The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology.The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 3/29/2024 |
| 3018 | BioLife Solutions Indianapolis, IN Aseptic Technician I Minimum: Two years of college-level biological coursework, i.e. in Chemistry, Biology, Physics, etc.Minimum: Two years of college-level biological cou Exp: Entry-level |
Daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is entry level and an effective way to get started in a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 3/29/2024 |
| 3019 | BioLife Solutions Bothell, WA Aseptic Technician II Bachelor’s degree. Exp: 1 year |
The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 3/29/2024 |
| 3020 | BioLife Solutions Bothell, WA Quality Specialist I Bachelor’s degree. Exp: 0-2 years |
The Quality Assurance Specialist is a core team member of the Quality department. The Quality Assurance Specialist ensures the Quality Management System (QMS) programs flow in a timely and accurate fashion, and that the programs are in compliance with all business requirements. Quality Assurance is a trusted partner to other departments and builds strong relationships both internally and externally. This position must demonstrate abilities to work cross-functionally throughout the company with superior communication skills. A motivated self- starter and attention to detail finisher is key to the core role of Quality Assurance, ensuring that all procedures are processed in a timely fashion and right the first time. | 3/29/2024 |
| 3021 | Biomerics Salt Lake City, UT Design Transfer Engineer I A bachelor’s degree in engineering or a related field (mechanical, biomedical, chemical) is required. (Required). Exp: 1+ years |
The Design Transfer Engineer I will be responsible for designing and manufacturing transfer of class II medical and surgical devices in a dynamic, customer-focused organization. The Design Transfer Engineer I will be expected to work with customers to understand product and process specifications, develop and transfer manufacturing processes, and build and test devices to those specifications. All activities will be expected to be documented according to design control requirements in a design history file (DHF). The Design Transfer Engineer I will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team. The Design Transfer Engineer I will work within the constraints of budget, schedule, and scope while managing risk and ensuring adherence to established processes & regulations. The Design Transfer Engineer I may be an individual contributor and participate as part of a small cross-functional team comprising engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. | 3/29/2024 |
| 3022 | Biomerics Brooklyn Park, MN Industrial Engineer A bachelor’s degree in industrial engineering or an engineering degree is required. Exp: 1+ years |
This position will play an integral role at BAC by driving and implementing continuous improvement throughout the business. The IE works cross-functionally across the plant to eliminate waste and improve product, material, and information flow. | 3/29/2024 |
| 3023 | Biotium Fremont, CA CHEMISTRY TECHNICIAN I (CHEMISTRY) B.S. or M.S. degree in Chemistry. Exp: 1+ years |
Under the direct supervision from a senior chemist, perform chemical purifications using chromatography including preparative HPLC or gravity chromatography; carry out chemical synthesis using standard protocols; carry out chemical analyses using modern instruments including analytical HPLC, LC-MS, TLC, UV/Vis and fluorescence spectrophotometry. | 3/29/2024 |
| 3024 | Biotium Fremont, CA RESEARCH ASSOCIATE I, BIOSCIENCE B.S. in Biology, Molecular Biology, Biochemistry or a related field. Exp: 1+ years |
Under direct supervision from the VP of Research and Development, perform synthesis, purification, and characterization of antibody/biomolecule conjugates of fluorescent dyes, fluorescent proteins, tandem dyes, enzyme reporters, and polymeric scaffolds. Research and development leading to commercialization of bioconjugates for research applications. The successful candidate will possess a strong background in chemistry and bioconjugation chemistry and have experience performing bioconjugation reactions, protein purification, and requisite analytical techniques. | 3/29/2024 |
| 3025 | Visby Medical San Jose, CA Product Transfer Engineer I Bachelor’s degree in engineering or related field. Exp: 1-2 years |
The Product Transfer Engineer plays a vital role in transitioning products from design and development to full-scale production. The individual will also be responsible for root cause investigations under the guidance of senior team members to ensure smooth operations. | 3/29/2024 |
| 3026 | Boston Analytical Salem, NH Analytical Chemist I, Raw Materials Qualification include a Bachelor’s degree in Chemistry or a related discipline is required. Exp: 0-2 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties include performing analysis of Raw Materials using AA, UV-Vis, and Wet Chemical Analysis according to USP/EP methods. | 3/29/2024 |
| 3027 | Boston Analytical Salem, NH Microbiologist QC I - Framingham Qualifications include a BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. Location: Framingham, MA | 3/29/2024 |
| 3028 | Boston Institute of Biotechnology Southborough, MA Research Associate – Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≤1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision. | 3/29/2024 |
| 3029 | Boston Institute of Biotechnology Southborough, MA Assoc. Scientist – Downstream Process Development MS degree in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≥1 year |
The Associate Scientist is responsible for development and execution of downstream related projects with moderate direct supervision. The individual reports to a more senior scientist level or above on relevant projects. The individual will provide expertise in the development and optimization of downstream processes. | 3/29/2024 |
| 3030 | KCAS Bioanalytical Olathe, KS Associate Scientist - Pharma LC-MS/MS Bachelor’s degree in Chemistry, Biochemistry, or related field. Exp: 1-3 years |
When you work as an Associate Scientist on the Pharma LC-MS/MS team, you get to further our mission by being a contributing scientist on studies, with the ability to carry out all aspects from study setup and development, through reporting with some assistance. You will need to utilize a strong base in scientific principles/theory to assess data integrity and troubleshooting, while independently completing experiments. | 3/18/2024 |
| 3031 | KCAS Bioanalytical Olathe, KS Analyst II - Pharma LC-MS/MS BS/BA degree in Chemistry, Biochemistry, or other life science field. Exp: one year |
When you work as an Analyst II in the Pharmaceutical Liquid Chromatography Mass Spectrometry (LC-MS/MS) lab at KCAS, you get to further our mission by working under senior Pharma LC-MS/MS scientists to contribute to the success of our clients. | 3/18/2024 |
| 3032 | Latitude Pharmaceuticals San Diego, CA QC Associate Minimum BS degree in Chemistry or chemistry-related field. Exp: 1+ years |
LATITUDE Pharmaceuticals Inc., a San Diego-based contract drug developer and manufacturer, is seeking a Quality Control Associate to be a key member of the QC group. A successful candidate should have some experience in drug product manufacturing and analytical testing techniques under GMP. This is a full-time position and will report to the Director of Quality. The position will be located in San Diego, California. | 3/18/2024 |
| 3033 | Lodo Therapeutics Cambridge, MA Operations Engineer 1, DNA Synthesis (Weekend Shift) at Ginkgo Bioworks Inc. Bachelor's degree in biology, biochemistry or biomedical engineering. Exp: 1+ years |
We're seeking a DNA Synthesis Operations Engineer to join our team to execute, improve, and scale our state-of-the-art manufacturing process flows. You’ll apply molecular biology protocols to perform efficient and high-quality lab-work in a fast-paced setting. You will use your excellent communication skills and flexibility to work effectively within a diverse team. You’ll display your breadth by leveraging the technology, software, automation, and instrumentation acumen required by our detailed processes flows. Please note that this position is to be filled at our Cambridge, MA location and will cover a four day, 10 hour per day work schedule (Thursday to Sunday - 10AM to 8PM). | 3/18/2024 |
| 3034 | Regulus Therapeutics San Diego, CA Temp/Hire: Research Associate – Senior Research Associate, Drug Discovery Biology MS in Biology or related discipline. Exp: 1+ years |
We are excited to invite a dedicated and driven individual to join our Research Biology team. This role is designed for a qualified candidate who seeks the opportunity to evolve as a drug discovery scientist, with a specific focus on microRNA biology, oligonucleotide therapeutics, and CNS-related diseases. The successful candidate will serve as a hands-on cell and molecular biologist, contributing valuable research experience and skills to the organization. The role encompasses a spectrum of drug discovery efforts, spanning early-stage target identification to advanced IND-related activities. The ideal applicant should possess direct experience in various molecular techniques, a robust understanding of cell biology, and excellent organizational and presentation skills. This position presents an exciting prospect to contribute to the exploration of innovative oligonucleotide therapeutics addressing areas of high unmet medical need. | 3/20/2024 |
| 3035 | AGC Biologics Seattle, WA Downstream Manufacturing Associate I/III Bachelor’s degree or Biotech certificate, quality systems regulations (cGMP) knowledge. Exp: 1+ years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. The Manufacturing Support Technician will be responsible for fulfillment of immediate requests from the Manufacturing Operations departments including, but not limited to, assembly preparation, washing parts, autoclaving of parts, kitting parts for delivery and facility sanitizations. The deadline for applications is the 31st of March. | 3/20/2024 |
| 3036 | AGC Biologics Boulder, CO Quality Assurance Associate I-III (In Plant Operations) Bachelor’s degree in Biology, Chemistry or other relevant science/engineering discipline. Exp: Associate II – 0 - 2 years |
The Quality Assurance Associate I- III (In Plant Operations) is responsible for providing (24/7/365) Quality support to the activities listed below at the Boulder, CO site. SCHEDULE: 2-2-3 Blue Days | 3/20/2024 |
| 3037 | AGC Biologics Seattle, WA Quality Control Associate I BS/BA degree. Exp: 1-3 years |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. | 3/20/2024 |
| 3038 | AGC Biologics Seattle, WA Upstream Manufacturing Associate I/III Bachelor’s degree or Biotech certificate, quality systems regulations (cGMP) knowledge. Exp: 1 year |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. The Manufacturing Support Associate will be responsible for fulfillment of immediate requests from the Manufacturing Operations departments including, but not limited to, assembly preparation, washing parts, autoclaving of parts, kitting parts for delivery and facility sanitizations. | 3/20/2024 |
| 3039 | AGC Biologics Seattle, WA; Boulder & Longmont, CO, US Upstream Process Development Associate I A.A./B.S. in a life science or engineering. Exp: 1-3 years |
This is a Development Associate I position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. The deadline for applications is the 31st of March. | 3/20/2024 |
| 3040 | Aptitude Medical System Santa Barbara, CA Research Associate Bachelor’s degree or Master’s degree in a relevant discipline. Exp: Entry-level |
We are seeking to hire multiple capable and driven entry-level Research Associates to join our tight-knit research and development team. In this position, you will be working closely with a cross-functional team of mission-driven scientists and engineers to drive the invention and development of novel diagnostic products. | 3/21/2024 |
| 3041 | Aura Biosciences Brighton, MA Sr. Associate Scientist, Upstream Degree in biochemical engineering, biological sciences, biochemistry or related discipline. M.S. Exp: 1+ years |
Reporting to the Upstream Process Development Lead, the (Sr) Associate Scientist will be responsible for the development of upstream production processes and the production of material for routine in-house development use. This includes all assays associated with cell culture production. The incumbent will also participate in the transfer of the upstream process to support biopharmaceutical product development at Contract Manufacturing Organizations (CMOs). The scientist will interact with the in-house team and the CRO/CMO to ensure timely progress in technology development, documentation, and manufacturing readiness. | 3/21/2024 |
| 3042 | Bio-Concept Laboratories Westborough, MA Entry Level Scientist 1 - 2nd Shift Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: Entry-level |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Sunday - Thursday 4:00 pm - 12:30 am What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3043 | Bio-Concept Laboratories Sheridan, WY Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory workJoin us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 3/21/2024 |
| 3044 | Bio-Concept Laboratories Westborough, MA Entry Level - Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Sunday - Thursday 8 am - 4:30 pm What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3045 | Bio-Concept Laboratories Mt. Juliet, TN Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory wor | 3/21/2024 |
| 3046 | Bio-Concept Laboratories Mansfield, MA Scientist 1 -Metals- Entry Level Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Find your place at Pace® Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Monday - Friday 3 pm - 11:30 pm What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3047 | Bio-Concept Laboratories Mansfield, MA Scientist 1 - Metals - Early Mornings Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Monday - Friday 5 am - 1:30 pm What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3048 | Bio-Concept Laboratories Greensburg, PA Environmental Scientist - Entry Level Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: Entry-level |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3049 | Biofactura Frederick, MD Quality Control Analyst Bachelor’s degree required. Exp: 1+ years |
The QC Analyst will support the establishment and growth of BioFactura’s QC department. Responsibilities include, but are not limited to, performing QC testing of DS/DP release and stability samples in support of BioFactura programs; ensuring compliance with established regulatory practices and standards; working with Analytical Development (AD) on the transfer of qualified assays to QC; assisting with assay validation activities; and authoring and review of SOPs, protocols, and reports. | 3/22/2024 |
| 3050 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline. Exp: 1 to 6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 3/22/2024 |
| 3051 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry. Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 3/22/2024 |
| 3052 | CRISPR Therapeutics Boston, MA Research Associate II, in vivo Oligonucleotide Chemistry MS degree in Chemistry, Chemical Engineering, Biochemistry, Bioengineering, Pharmaceutical Sciences or related field. Exp: 1+ years |
CRISPR Therapeutics is seeking a highly motivated Research Associate to join our In Vivo Technical Operations department in Boston, Massachusetts. The incumbent will be responsible for the oligonucleotide synthesis, purification, desalting, and analysis to support the process development of guide RNA production in various scales. This position will also support therapeutic programs in multiple disease areas in R&D department. Prior experience in oligonucleotide synthesis, purification, and characterization is desired | 3/22/2024 |
| 3053 | GenEdit South San Francisco, CA Lab Technician, Chemistry (Part Time) Associate degree (or) bachelor’s degree in any science field or equivalent experience. If the candidate is willing to be promoted to RA I, the positio Exp: RA I: 0-2 years |
GenEdit is seeking a highly self-motivated Lab Technician to provide support to the Chemistry team. The Lab Technician will be responsible for assisting the Medicinal Chemistry Team in cataloging and organizing the inventory of synthesized polymers, alongside routine lab maintenance and aliquot distribution. They will have a key role in chronicling the various modes of organic, polymer, and analytical chemistry performed at GenEdit. A successful candidate will be collaborative, resourceful, and enthusiastic to work in a team environment. This candidate will report to the Principal Scientist in the Chemistry Department and communicate with all interdisciplinary groups like formulation, in vitro and in vivo teams. This position may convert into a full time Research Associate (RA I) in a year subject to candidate’s performance and the requirement by the Chemistry department. Upon promotion to RA, the candidate will be working in organic synthesis of bio-synthetic polymer, macromolecule and/or complex organic molecule characterization utilizing various separation and detection techniques in support of research, regulatory and business efforts. They will be responsible for synthesis of novel polymer molecules, assist with developing, implementing, and validating analytical methods to characterize novel polymers for gene delivery nanoparticles. This position will also participate in the development and routine performance of polymer characterization assays for identity and purity, preparation of certificates of analysis (COA), and preparation of standard operating procedure (SOP). Additional duties and responsibilities may be required as needed. | 3/22/2024 |
| 3054 | Immucor Norcross, GA MQA Technician II Associate’ Degree (AA) or equivalent from a two-year college or technical school; Bachelor’ degree is highly preferred. Exp: six months to one year |
We are seeking an experienced Manufacturing Quality Assurance (MQA) Technician II to join our team. Our company is a growing medical technology firm that offers challenging positions, opportunities for professional growth, and competitive benefit packages to all employees. Our company is founded on and guided by our corporate mission and values: respect, integrity, teamwork, and achievement. If you have the necessary skills and experience to excel in this position, we want to hear from you! | 3/22/2024 |
| 3055 | Indivior Raleigh, NC Controls Engineer Bachelor of Science in Engineering or related field. Exp: 1+ years |
The Controls Engineer is a technical resource to the engineering, maintenance, validation and operations departments, to meet all regulatory and Company specific policy requirements and objectives, and to improve plant efficiency, capacity, capability and modernization. This person is responsible for the research, development, design, layout, building, testing, troubleshooting, repairs and improvement of all manufacturing control systems, including the Building Management System (BMS), HVAC, and Utility Control Systems. The position is also responsible for implementing improvements to increase equipment efficiency and prevent obsolescence, as well as ensuring the validated state of all applicable equipment, systems and facilities. This position will maintain compliance with all company standard operating procedures (SOPs) and applicable cGMP, OSHA, EPA, and local government regulations. | 3/22/2024 |
| 3056 | Indivior Raleigh, NC Environmental Monitoring Technician II Bachelor of Science degree in a life science or equivalent. Exp: 1-3 yrs |
This position reports to the EM Supervisor for the functional area to which they are assigned and has no direct reports. This individual holding the position of EM Technician II shall be responsible for performing routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms, critical utilities and controlled environments. | 3/22/2024 |
| 3057 | Lampire Biological Labs Everett, PA Laboratory Technician BS in relevant field. Exp: 1-2 years |
Job Description: To facilitate daily operations at the Coopersburg Laboratory by supporting the whole blood, plasma/serum, anticoagulant, brokered and abattoir departments as necessary. | 3/22/2024 |
| 3058 | NeuMoDx Molecular Ann Arbor, MI MANUFACTURING SPECIALIST, REAGENT College Degree (BS/BA) in science or chemistry field. Exp: 1 year |
Manufacturing Specialists are required to have a strong knowledge of manufacturing methods and techniques, process development experience, work flow understanding, ability to understand formulations and follow recipes and testing protocols for any in-process Quality checks • In this position, Manufacturing Specialists, will maintain manufacturing equipment, create work instructions, train others, often be asked to contribute to or lead projects, be cross functionally trained to work in several areas as needed. • This role requires a self-starter, ability to work independently, understanding of departmental goals-working as a team to achieve those goals within set timelines. | 3/22/2024 |
| 3059 | Physical Sciences Andover, MA Chemical Engineer BS or MS degree in Chemical Engineering, Chemistry or Materials Science. Exp: 0 to 2 years’ |
Physical Sciences Inc., located just north of Boston in Andover, has a career opportunity for a Chemical Engineer with a strong background in reaction kinetics, heat and mass transfer, and separations. We are seeking an applicant who can assist with developing and scaling-up materials production from laboratory/batch processes to pilot-scale/continuous processes. The applicant we seek would benefit from material development, purification and characterization experience. We are looking for a strong worker, who can safely and effectively execute on their ideas as a member of a team and sometimes as an individual contributor. This Chemical Engineer will be asked to work on innovative programs, in areas such as atmospheric water harvesting, continuous process development, and waste conversion to high performance materials. Experience with wet chemistry laboratory procedures and related analytical techniques is essential. Hands on experience with hardware assembly for chemical processes is preferred. Working knowledge of analytical laboratory techniques (e.g. GC-MS, FTIR, NMR, DSC, TGA, tensile testing) and chemical engineering software packages (e.g. Comsol) is highly desirable. | 3/22/2024 |
| 3060 | Physical Sciences Andover, MA Optical Engineer Bachelor’s degree in optical or mechanical engineering, physics or equivalent. Exp: 1+ years |
Physical Sciences Inc., a 100% Employee-Owned company located just north of Boston in Andover, seeks an Optical Engineer with professional experience to support development of emerging optical technologies. The candidate will support optical systems design, construction, and testing needs for illuminators, projectors, integrated spectrometers and/or metasurfaces. A strong basic understanding of optical system layout and construction is sought. | 3/22/2024 |
| 3061 | Physical Sciences Andover, MA Experimental Physicist Bachelor or Masters degree in Physics, Applied Physics, Optics, or Related Discipline. Exp: 0-5 years |
Physical Sciences Inc., located just north of Boston in Andover, MA, seeks an experimental physicist with experience in laser-based tools related to applications such as atom sensing, integrated photonics, or optical materials development. The candidate will join teams at PSI and contribute to invention, demonstration, and deployment of technology platforms targeting these application areas. The ideal candidate will have a bachelor’s or master’s degree in physics or related disciplines and should be interested in applied research and development with strong experimental, hardware, and leadership skills. | 3/22/2024 |
| 3062 | The Ritedose Corporation Columbia, SC Microbiologist Technician Technical degree in life science or related field. Exp: 1+ years |
The Microbiologist Technician is responsible for all duties related to performing environmental monitoring, personnel monitoring. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining and ordering inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. | 3/22/2024 |
| 3063 | Sedia Biosciences Beaverton, OR Production Technician I High School diploma, Training Certificate, or Associates degree (technical field preferred). Exp: Entry level |
Production Technicians at Sedia will be responsible for the production of Sedia’s products. This includes the formulation of reagents, application of reagents to various materials, dispensing of testing reagents into vials, tubes, or bottles, capping and labeling of components and assembly of components into finished test kits. Technicians will be working with standard laboratory equipment as well as automated and semi-automated production equipment. | 3/22/2024 |
| 3064 | Sedia Biosciences Beaverton, OR QC Technician I High School diploma, Training Certificate, or Associates degree (technical field preferred). Exp: Entry-level |
This position works under direct supervision to perform Quality Control functions including the inspection and testing or raw materials, components, and finished products in a medical diagnostic manufacturing environment. Works in compliance with the Quality Management System and under applicable quality standards such as ISO-13485 and CFR 21 part 820 cGMPs. | 3/22/2024 |
| 3065 | Acceleron Pharma Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 3/22/2024 |
| 3066 | Acceleron Pharma Rahway, NJ Specialist, Process Engineering Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Sterile GMP Clinical Manufacturing facility. As the facility is nearing the completion of its construction, the selected candidate will contribute to equipment and facility commissioning/qualification, regulatory certification, as well as other workstreams’ critical activities to enable facility startup and operational readiness. To support these business-critical activities, night and weekend work may be required. Once the facility is operational, this role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of sterile clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 3/22/2024 |
| 3067 | Acceleron Pharma Rahway, NJ Specialist, Analytical Research and Development Advanced and relevant industry experience for applicants with a Bachelor of Science degree, or beginner, relevant industry experience for applicants w Exp: 1+ years |
The Small Molecule Analytical Research and Development group has an opening for a Specialist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Specialist, you will be part of a team of Specialists working on cross-functional scientific teams to enable development of novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization of our raw materials including excipients and package components. | 3/22/2024 |
| 3068 | Acceleron Pharma Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 3/22/2024 |
| 3069 | Acceleron Pharma Rahway, NJ Specialist, Quality Assurance (Hybrid) Bachelor degree (B.S.) in an appropriate Science or Engineering discipline (engineering, chemistry, biology, biochemistry, microbiology). Exp: 1+ years |
The Rahway based Specialist, Global Development Quality Operations - API, is responsible for review and approval of documentation to support Good Manufacturing Practice (GMP) clinical supply API manufacture, testing, release and maintenance in support of our company's clinical supply programs. This person will also review and approve documentation accompanying the disposition of API materials (including new modalities) to ensure conformance to appropriate regulatory and company requirements for clinical supply manufacture and/or regulatory inspections. Performs audits of batch documentation, data, information, procedures, equipment and systems, and/or facilities to ensure the compliance with Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMPs) and other applicable worldwide regulations and our Company procedures. The Specialist will become knowledgeable in regulatory requirements, cGMPs and our company's procedures to assure API (including new modalities) manufacturing and testing is in compliance and will gain competency in their responsibilities. | 3/22/2024 |
| 3070 | Tris Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field. Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. | 3/11/2024 |
| 3071 | Turn Biotechnologies Mountain View, CA Research Associate - Synthetic Chemistry, CMC BS/MS in organic/synthetic chemistry or related discipline. Exp: 1-3 years |
Turn Biotechnologies is seeking an excellent Research Associate with strong knowledge and hands on experience in synthetic/organic chemistry to work in our CMC team. The ideal candidate should have experience in synthesizing, purifying and characterizing small molecules, in particular lipids. Additionally, experience in polymer chemistry is a plus. | 3/11/2024 |
| 3072 | Vor Biopharma Cambridge, MA GMP Operations Associate BS in Biology or related field. Exp: 1 - 3 years |
Vor Bio is seeking a GMP Operations Associate who is an enthusiastic and driven individual to support cGMP manufacturing for clinical phase cell therapy manufacturing facility. The candidate will be responsible for providing assistance in the support area for the manufacturing of Vor’s gene-edited cell therapies and maintaining compliance of cGMPs in manufacturing areas. | 3/15/2024 |
| 3073 | Wright Medical Portage, MI Electrical Design Engineer Bachelor's degree in EE or related discipline required. Exp: 0+ years |
This role is on the Electrical Engineering team at Stryker Medical division's Acute Care business unit. We primarily work with patient handling and patient care equipment within the hospital space such as stretchers, hospital beds, and support surfaces. This role falls under the team addressing the high-acuity market, with a focus on products that often come into direct contact with patient. It includes gaining a deep understanding of customer needs through research and partnership with upstream marketing and through direct interactions with customers. Working with a diverse team, you will design, develop, modify, evaluate, and verify electrical components and sub-systems for medical devices. The role includes the full development process from research to product launch. | 3/15/2024 |
| 3074 | Wright Medical Mahwah, NJ Operations Engineer Bachelor’s degree in engineering- Required. Exp: 1 year |
Stryker Orthopedics is seeking to hire an Operations Engineer to support the manufacturing of joint replacement products in Mahwah, New Jersey. As an Operations Engineer with the operations team you will provide manufacturing engineering support and direct projects for assigned cells. | 3/15/2024 |
| 3075 | ZeptoMetrix Raleigh, NC Production Scientist I Bachelor’s degree in Chemistry, Engineering or related field from an accredited higher learning institution. Exp: Up to 2 years |
The Production Scientist I will involve all manufacturing tasks related to the production of the company’s organic products. Responsibilities include manufacturing, handling, and packaging various classes of organic compounds as per standard operating procedures. The incumbent must be a dynamic individual who can multi-task and perform various activities associated with manufacturing operations while adhering to all safety policies and high quality Standard Operating Procedures. This position requires hands on chemistry lab work and will report to the Organic Manufacturing Lead. | 3/15/2024 |
| 3076 | ZeptoMetrix North Charleston, SC Scientist I, Quality Bachelor's degree in Chemistry or related field. Exp: 1 year |
The Quality Control (QC) Scientist is primarily responsible for the quality control of starting materials, in-process materials and the finished goods. The incumbent must be a dynamic individual who can work in a diversified group and able to handle multi-tasks within QC operations. The candidate must possess a good working knowledge of Analytical Chemistry. This position requires hands on chemistry lab work and troubleshoot instruments and solve complex spectroscopic problems. | 3/15/2024 |
| 3077 | Zimmer Biomet Warsaw, IN Development Engineer I Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mec Exp: 1 - 3 years |
*Please note, this role is a hybrid position, partially onsite in Warsaw, IN and partially remote. You have a key support role with responsibility for new product design, development, and commercialization; and/or to maintain in the market innovative medical device products in order to further Zimmer Biomet’s mission and grow Zimmer Biomet’s market leadership position | 3/15/2024 |
| 3078 | Zimmer Biomet Warsaw, IN Technician College/University courses in Microbiology, Biology, Chemistry, Engineering Mechanics, Medical Technology or other related field preferred. Exp: 0 – 3 years |
Responsible for supporting the daily operations of the laboratory at all Zimmer Biomet Warsaw facilities and for operating and maintaining laboratory equipment for the necessary assigned tasks per area work instructions. May also be responsible for ensuring that equipment calibration and maintenance (preventive and/or corrective) is performed. | 3/15/2024 |
| 3079 | Zimmer Biomet Warsaw, IN Development Engineer I Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mec Exp: 1-3 years |
*This is a hybrid position, partial remote/partially onsite, in Warsaw, IN. Responsible for the design, development, and processing of patient specific implants and instruments based upon individual patient anatomy or conditions. Work is expected to encompass both the development of new products and maintenance of existing products. Position will lead small scope project as a project leader or portions of larger scope project as a core team member as well as individual patient cases within the Patient Matched Implants (PMI) department. | 3/15/2024 |
| 3080 | Z-Medica Morrisville, NC Associate R&D Engineer, Sustaining Possession of bachelor’s degree in engineering. Exp: One year |
This is an entry level engineering position that will support the sustaining engineering group for the Emergency Medicine product families. However, assignments may include work for other products within the Teleflex portfolio. Experience and background requirements should focus on disposable products. Incumbent organizes and manages multiple projects and ensures projects are completed in a timely manner; Assignments may focus on sustaining engineering assignments providing creative solutions to existing products when problems arise, or modifications are requested. Performs other duties as required or assigned. | 3/15/2024 |
| 3081 | Z-Medica Morrisville, NC Associate R&D Engineer, Sustaining Possession of bachelor’s Degree in Engineering. Exp: One year |
This is an entry level engineering position that will support the sustaining engineering group for the anesthesia products lines. However, assignments may include work for other products within the Teleflex portfolio. Experience and background requirements should focus on disposable products. Incumbent organizes and manages multiple projects and insures projects are completed in a timely manner; Assignments may focus on sustaining engineering assignments providing creative solutions to existing products when problems arise, or modifications are requested. Performs other duties as required or assigned | 3/15/2024 |
| 3082 | Z-Medica Jaffrey, NH Associate Manufacturing Engineer Bachelor's Degree in Polymer/Plastics Engineering or equivalent field required. Exp: 0-2 years |
Results-driven professional is dedicated to constant learning and training. We are looking for an Polymer or Chemical Engineer to join our team. You will be responsible for assisting, planning, designing, and completing projects in extrusion manufacturing utilizing six sigma/lean/DMAIC or like methodologies. The ideal candidate would have experience working with manufacturing equipment and processes to optimize production and increase capacity. Must have equipment acumen, with the ability to be creative and troubleshoot when necessary. Technical aptitude, people-centric, and ability to assist the PTFE and melt extrusion departments. | 3/15/2024 |
| 3083 | Z-Medica Maple Grove, MN Environmental Technician Bachelor’s Degree in Biology, Chemistry, Microbiology or other related science or engineering field. Exp: 0 - 2 years |
Responsible for the environmental/microbial control in the Teleflex manufacturing facilities. Complete planning, coordination and execution of deliverables related to environmental control, microbial control, sterilization qualifications and cleaning/disinfection control of manufacturing areas. | 3/15/2024 |
| 3084 | Z-Medica Maple Grove, MN Microbiologist I Bachelor’s Degree required in a related scientific discipline. Exp: No previous professional experience required. |
This role is responsible for complete execution of deliverables related to microbiology testing, contamination control, cleaning/disinfection validation of manufacturing areas, product release testing, and controlled environment monitoring/certification. This will require review of samples to ensure testing is performed according to provided work instruction. Fulfill microbiology role supporting new product development, production, controlled environments, and sterilization. | 3/15/2024 |
| 3085 | Z-Medica Morrisville, NC Service Engineer Minimum AA/AS/BS or demonstrated equivalent. Exp: 1 year |
This individual is responsible for the troubleshooting, service and repair of VPS products following established procedures and work instructions at the Morrisville, NC Service Center. They will support critical business activities related to servicing VPS capital equipment products focused on the customer experience, continuous improvement and workflow efficiencies This role will collaborate with VPS service globally, working with other Teleflex sites, third parties and distributors to maintain a consistent approach to service | 3/15/2024 |
| 3086 | Zymo Research Irvine, CA Bioinformatics Associate I Holds a master’s or bachelor's degree in Biology, Bioinformatics, Computer Science, Mathematics, Statistics, or a related discipline. Experience may s Exp: 1+ years |
Zymo Research is seeking a highly motivated individual to join our Bioinformatics team! The qualified individual will play a key role in developing analysis pipelines for Next-Generation Sequencing data and performing cutting-edge data science to support Zymo Research’s global product strategy. As part of the Bioinformatics team, you will leverage your skills and familiarity with NGS-based sequencing methods in the research and development of new data analysis pipelines for our services, applications, and exciting research projects! | 3/15/2024 |
| 3087 | ZebraSci Mannford, OK; Tempe, AZ; Vernon Hil, OK R&D Engineer II B.S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other related engineering field. Mechanical Engineering degree Exp: 1-3 years |
Hybrid, Multiple Locations. This position is a limited term assignment which will include benefits such as (medical, health, dental, 401K). Eligibility for these benefits will be based on the eligibility requirements as determined by the BD Total Rewards policy and is anticipated to last approximately through 12/20/24. This position works multi-functionally and leads R&D activities needed in the development and transfer to manufacturing of products, processes, test methods and equipment for medical device manufacturing. Hybrid, Multiple Locations. This position is a limited term assignment which will include benefits such as (medical, health, dental, 401K). Eligibility for these benefits will be based on the eligibility requirements as determined by the BD Total Rewards policy and is anticipated to last approximately through 12/20/24. This position works multi-functionally and leads R&D activities needed in the development and transfer to manufacturing of products, processes, test methods and equipment for medical device manufacturing. | 3/15/2024 |
| 3088 | ZebraSci Lexington, MA Analytical Chemist Bachelor of Science degree required; Master of Science degree preferred. Exp: 1-year |
This position will be involved in many aspects of producing and developing biomaterials, including the analysis, production, isolation, purification and testing of biomaterials within well-defined guidelines. The associate will need to use appropriate analytical tools to characterize and qualify the biomaterials, such as gas chromatography (GC), gel permeation chromatography (GPC) and mechanical testing. S/he will interact with contract testing laboratories to conduct appropriate testing on the materials and may also provide supervision and guidance to junior level technicians. | 3/15/2024 |
| 3089 | ZebraSci Branchburg, NJ Combination Product Test Engineer Bachelors of Engineering, Biomedical, Chemistry, Biology, or equivalent is preferred. Exp: 1+ years |
Responsibilities Conducts timely sample intake, including receipt, proper identification, storage and return shipments as needed Conducts testing as assigned utilizing appropriate test methods, protocols specifications and equipment (includes product and/or equipment testing), including adhering to test schedules (e.g. stability pulls, aging pulls). Conducts data analysis as per protocol or specifications utilizing variety of data analysis tools (e.g. excel, JMP, MiniTab) Communicate challenges, scheduling or testing conflicts and other issues to management in timely manner Maintains inventory of lab supplies, including but not limited to; general supplies (e.g. PPE, wipes, cleaners…) and chemicals use for routine testing and/or cleaning Conducts routine sample disposition (e.g. return to client, disposal), including coordination of hazardous waste disposal Responsible to maintain the lab and storage areas in a clean an organized manner. Includes routine lab cleaning Adheres to ZebraSci Quality Systems, including but not limited to; timely identification, and notification of potential Quality Events (e.g. OOS, Deviations, CAPA…) and the subsequent forward processing and investigation of such events | 3/15/2024 |
| 3090 | ZebraSci Louisville, CO Staff Reliability Engineer BS in engineering or a related technical field (i.e., physics, materials science, mathematics). BS in engineering or a related technical field (i.e., Exp: 1-year |
The Staff Reliability Engineer is responsible for providing project support to ensure reliability targets are achieved according to project plans. The reliability engineer should have a demonstrated broad technical base in all aspects of reliability engineering. The ideal candidate would have experience in electrical, mechanical and software engineering fundamentals, including PoF (Physics of Failure) understanding. The candidate will work closely with R&D members and be a sole contributor to conduct system and component level reliability activities for sustaining product and new product development within the franchise and division. The reliability engineer will have the technical skills necessary to effectively challenge the design concepts as they pertain to overall reliability. An exciting part of the role includes opportunities to work on reliability initiatives for key R&D business critical projects. At the heart of reliability engineering is testing and we are looking for expertise that will help us become a Center of Excellence. The reliability engineer will lead troubleshooting and failure analysis investigation activities to determine design weaknesses and root-cause. Ideally the candidate will grow and be able to direct efforts of individuals around reliability process and deliverables | 3/15/2024 |
| 3091 | ZebraSci Temecula, CA Combination Product Test Engineer (Onsite) Bachelor’s degree in science or math related fields, such as biology, chemistry or engineering is preferred. Exp: 1 year |
The primary role of the Engineering Technician is the timely and accurate execution of testing as scoped within individual projects and per client requirements. This includes but is not limited to; sample receipt, prep, storage, and shipping, as well as protocol and report generation, data review and summary. This role utilizes standard and custom laboratory equipment. | 3/15/2024 |
| 3092 | ZebraSci Mebane, NC Associate Quality Scientist Bachelor’s degree in Biology, Microbiology or other related Life Science. Exp: 1-2 years |
Reporting to the Quality Scientist/Lab Supervisor, the BD Mebane Associate Quality Scientist is responsible for applying basic scientific principles to routine laboratory work, executing product testing, applying/interpreting scientific data of moderate complexity, ensuring good laboratory practices, and processing data generated from Quality Control testing. | 3/15/2024 |
| 3093 | ZebraSci Columbus, NB Quality Engineer I Bachelor's Degree Required Field(s) of Study: Science-related field, Quality Assurance, Engineering, Mathematics/Statistics Exp: 0-5 years |
Support Quality and Production groups by using process and regulatory knowledge combined with a data driven approach to problem solving. Become a subject matter expert in application of statistical tools, measurement systems analysis, and root cause analysis. Take ownership of projects and drive to completion, whether working independently or in a team. Will interact professionally with BDM, PS customers in project management and problem solving activities. Regular, punctual attendance is an essential job function. Ability to speak, read and write English. Ensures compliance with BD quality systems, policies, procedures and practices and all local, state, federal and BD safety regulations, policies and procedures. The applicant pool includes an identified internal candidate. All applications are welcomed | 3/15/2024 |
| 3094 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology. Exp: 0-3 years |
The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. If interested, please send your resume to hr@accurusbio.com. | 3/15/2024 |
| 3095 | Affinivax Rockville, MD Biopharmaceutical Associate I Bachelor of Science / Bachelor of Art / Associates Degree in biological sciences, chemical sciences, engineering or equivalent technical discipline. Exp: 1+ years |
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Basic understanding and knowledge of the following areas and ability to perform the activity with some supervisory guidance: Follow appropriate standard operating procedures (SOPs), protocols and batch records/logbooks to safely perform process operations and document compliantly with good documentation and data integrity practices. Perform the set-up, operation, cleaning and break-down of process equipment. Perform sampling procedures on various analytical instruments to analyze cell culture, solution and/or product concentration characteristics. Operate Filter integrity devices to confirm the integrity of filters pre and post use. Perform process operations, equipment and instrument monitoring and trending to enable proactive identification of issues to escalate and correct with applicable departments. Follow all related safety policies and procedures and Put safety first by playing an active role in identifying and correcting unsafe behaviors and conditions. | 3/15/2024 |
| 3096 | Affinivax King of Prussia, PA Biopharm Manufacturing Associate II BS/BA degree OR an Associate’s degree from Montgomery county community college in Biotechnology or related technical field. Exp: 1+ years |
Posted Date: Mar 15 2024 Thank you for your interest in our Bio Pharm Manufacturing Associate II (Evergreen) position. Applicants for this role will not be receiving immediate feedback regarding their applications. If you are looking for an immediate opportunity, please take a look at the GSK careers page for opportunities that would align with your skill-set. I have included the link here for your convenience: Careers | GSK US . As a Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. | 3/15/2024 |
| 3097 | Affinivax King of Prussia, PA Associate Manufacturing Specialist Bachelors of Science, or Bachelors of Arts. Exp: 1+ years |
The Associate Manufacturing Specialist will be part of a high performing team responsible for delivering the supply of GSK products to the One Biopharm supply chain. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. The associate manufacturing specialist, with support from team leads and supervisors, will perform a mix of tasks ranging from operation of GMP equipment, to leading pieces of work associated with supporting new product introduction and/or improvement of existing processes. The work this role will support will follow the lifecycle of new products, more specifically: Equipment/Facility Design, Technology Transfer, Commissioning & Qualification, Start-up & Engineering Batch manufacture, Process Performance Qualification batch manufacture, Clinical Supply, Commercial Supply, Changeover, Process Improvement. | 3/15/2024 |
| 3098 | Affinivax King of Prussia, PA Associate Microbiologist BS in science field. Exp: 1+ years |
GSK is currently looking for an Associate Microbiologist to join our team in Upper Merion, PA. In this role, the Microbiologist performs quality testing for In process and bulk biopharmaceutical ingredients, finished biopharmaceutical products. Reviews and revise SOP’s when needed. | 3/15/2024 |
| 3099 | Affinivax King of Prussia, PA Manufacturing Specialist Bachelors of Science, or Bachelors of Arts. Exp: 1+ years |
The Associate Manufacturing Specialist will be part of a high performing team responsible for delivering the supply of GSK products to the One Biopharm supply chain. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. The associate manufacturing specialist, with support from team leads and supervisors, will perform a mix of tasks ranging from operation of GMP equipment, to leading pieces of work associated with supporting new product introduction and/or improvement of existing processes. The work this role will support will follow the lifecycle of new products, more specifically: Equipment/Facility Design, Technology Transfer, Commissioning & Qualification, Start-up & Engineering Batch manufacture, Process Performance Qualification batch manufacture, Clinical Supply, Commercial Supply, Changeover, Process Improvement. | 3/15/2024 |
| 3100 | Affinivax Hamilton, MT QC System Support Specialist Bachelor's Degree in a scientific discipline. Exp: 1+ years |
The QC Systems Support Specialist will manage non-testing laboratory support systems and processes for QC, including: Maintaining SAP Modules, Master Data/Monograph Creation, Compendial Review, Equipment Qualification/Lifecycle, and Method Validation/Transfer. Serve as a Lead Investigator for select QC Unplanned Events, as well as change coordinator for selected QC Change Controls. Author QC Technical Documents, such as validation and trend reports and provide data for annual PQR. Works collaboratively with global teams (ASAT) and the GSK network to maintain compliance and alignment, and to deliver both local and global projects as per established timelines. | 3/15/2024 |
| 3101 | Carmot Therapeutics Berkeley, CA Research Associate I/Research Associate II, Pharmacology BSc, MSc in pharmacology, biology or related field. Exp: 1-5 years |
In this position, you will assist with the design and execution of in vivo pharmacology experiments in rodents. In particular, you will be utilizing mouse models of obesity and diabetes to support compound characterization and mechanism of action studies. These efforts will support lead discovery and translational biology for clinical compounds. The position may also involve in ex vivo and in vitro pharmacology experiments. The environment at Carmot is fast paced, requiring you to be excellent at multitasking and working within a team to achieve common goals. | 3/15/2024 |
| 3102 | Cirtec Medical Sturtevant, WI Engineer I Manufacturing A bachelor’s degree in engineering. Exp: 0 years |
This position is primarily responsible for developing and implementing robust cost-effective manufacturing processes and methods in accordance with product specifications and Class III medical device quality standards. This position recommends and implements improvements to sustained production processes, methods and controls; as well as coordinates the launch of new products into pilot production. | 3/15/2024 |
| 3103 | Integrity Bio/ LyoTip Albuquerque, NM Mechanical Engineer Bachelor's degree (B.S.) in Mechanical Engineering. Exp: Entry level |
The Engineering Department provides the capacity to manufacture pharmaceuticals in an efficient, timely, and safe manner, thereby contributing to the profitability of the business unit by maintaining or modifying production equipment and related systems. The Mechanical Equipment Engineer will work in supporting manufacturing operations both on the manufacturing floor and off, spending time within the manufacturing operations is required and will be a priority at times. | 3/15/2024 |
| 3104 | Integrity Bio/ LyoTip Springfield, MO Process Engineer I or Process Engineer II The following required knowledge and proficiency skills are required for this position to be acquired through a minimum of a Chemical Engineering degr Exp: PE I: 0-3 years; PE II: 1-3 years. |
The primary purpose of the Process Engineer position is to design, implement and continuously improve chemical manufacturing processes using appropriate chemical engineering and scientific principles. Process design involves preparation of process flow diagrams, piping and instrument diagrams, mass and energy balances, equipment specifications, process safety information and operating procedures necessary to implement the process. Implementation involves development of construction task lists, participating in risk assessments, performing training, supporting start up and leading troubleshooting efforts. Continuous improvement includes identification of opportunities to improve quality, safety and economic performance of processes through proactive engineering evaluation as well as incident investigation and corrective/preventative action identification and implementation. Secondary purposes include configuration, modification and optimization of site control systems and to provide technical assistance to other site departments (QA, QC, Accounting, Maintenance, EH&S, etc.) in support of Curia's general business objectives and requirements. | 3/15/2024 |
| 3105 | Integrity Bio/ LyoTip Albany, NY Research Scientist I; Analytical Development Bachelor’s or Master’s Degree in Chemistry or a related field. Chemical Hygiene training. Exp: 1+ years |
The Research Scientist I-Analytical Development is an integral part of the Curia team, contributing to our success by supporting the manufacturing department and external customers. The routine functions of the laboratory are testing of raw materials, in-process, end product, and stability samples. The principal responsibility of the Research Scientist I is the analysis by multiple procedures of compounds. The Research Scientist I is expected to demonstrate proficiency in both the theoretical and practical aspects of analytical chemistry. | 3/15/2024 |
| 3106 | Integrity Bio/ LyoTip Albany, NY Research Scientist I; Analytical Development Bachelors or Masters Degree with major in Natural Science or Pharmacy or equivalent. Chemical Hygiene training. Exp: 1+ years |
The principal responsibility of the Research Scientist I is the analysis by multiple procedures of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. A major component in the scientist's performance rating will be based on productivity. | 3/15/2024 |
| 3107 | Integrity Bio/ LyoTip Rensselaer, NY Production Technician in Rensselaer, NY - 12 Hour Nights Associates or Bachelor's degree. Exp: 1+ years |
The Production Technician is an integral part of the team, contributing to our success by weighing out chemicals and preparing various types of solutions for use in process. | 3/15/2024 |
| 3108 | Integrity Bio/ LyoTip Burlington, MA Quality Assurance Specialist I, Sun-Wed 7a-5p Bachelor’s degree (or foreign equivalent) in Biology, microbiology, biotechnology or related life science field. Exp: 0-3 years’ |
The Quality Assurance Specialist I is responsible for maintaining Quality databases and providing on-the-floor QA presence and oversight to the manufacturing operation. The QA Specialist’s role will include identifying compliance risks in the operation prior to and during execution, avoiding deviation whenever possible as well as managing immediate corrective action such that a) adherence to cGMP’s and internal procedures/policies is maintained, b) appropriate immediate corrective action is implemented and effectively documented in order to provide traceability and substantiation of any claims to be made in the investigation. This position primarily works in the cGMP production areas to manage adherence to the quality system and to initiate and assist in the initiation and resolution of deviations. | 3/15/2024 |
| 3109 | Integrity Bio/ LyoTip Albuquerque, NM Aseptic Core Monitor I BS, preferably in Microbiology or a related field. Exp: 1+ years |
Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Aseptic Core Monitor (Albuquerque, NM) will oversee all activities in the aseptic environment to ensure continual compliance with cGMP and provide mentoring on aseptic techniques for all aseptic personnel. This position requires expertise in all aspects of aseptic manufacturing of the sterile product, the ability to work hands-on, strong leadership skills, and the ability to collaborate in a cross-functional environment. The individual will work closely with all departments in the manufacturing environment and reports metrics to site management regularly. Join our talented workforce, where a commitment to excellence and a customer-focused attitude is everything. We pursue excellence because our work has the power to improve patient’s lives with the pharmaceuticals we develop and manufacture. | 3/15/2024 |
| 3110 | Roche Seattle, WA Research Associate Bachelor’s, Master’s or PhD degree in Biological/Life Sciences, Chemistry, Organic Chemistry, Chemical Engineering, Biochemistry or related field. Exp: 1+ years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its unique chemistry that advances DNA sequencing by nanopore, Sequencing by eXpansion (SBX™). You will develop, process and purify the molecular building blocks for our novel technology. These building blocks translate DNA sequences into a simple to measure surrogate, the Xpandomer, which significantly improves the accuracy and throughput of nanopore sequencing. The Molecular Engineering group is passionate about the novel molecules they have developed and the impact SBX technology can have on advancing sequencing and patient outcomes. We are looking for people who are excited to collaborate with us to make SBX successful. Please include a cover letter outlining why you want to work with us, your specific interest in our technology and how you would contribute. | 3/5/2024 |
| 3111 | Roche Branchburg, NJ Senior Lab Technician Associates degree required; Bachelor's Degree preferred. Exp: < 1 year |
Branchburg is the molecular diagnostics manufacturing engine within Global Operations and a Polymerase Chain Reaction (PCR) center of excellence. As the largest DIA manufacturing site in North America, our teams deliver a broad portfolio of PCR-based in-vitro diagnostic tests. Our operations include reagent and active diagnostic ingredient (ADI) production, filling and packaging. Our 63-acre site with ~1400 people is currently under expansion, fueled by our culture of agility, innovation and transformation. Each day we focus on delivering the value of Roche Diagnostics to patients around the world. | 3/5/2024 |
| 3112 | Roche Carlsbad, CA Mechanical Engineer I BS degree. Exp: 0-2 years |
We are looking for a highly motivated and team-oriented individual who is passionate about technology and product development for IVD assays. As a Mechanical Engineer I, you will work under supervision from senior contributors for concept-to-market and sustaining engineering efforts of IVD instrumentation. Apply hands-on involvement in on-market support for existing and new products, troubleshooting and root cause analysis, creation and maintenance of input and output specifications, concept and feasibility activities, prototyping, testing, and transfer to manufacturing. | 3/5/2024 |
| 3113 | Roche Santa Clara, CA Product Engineer B.S. in Biology, Chemistry, Biochemistry, Molecular Biology, Mechanical Engineering or a related field. Exp: 1-3 years |
As a Product Engineer at Roche Sequencing Solutions, you will be instrumental in the development of the consumable prototype manufacturing process. In this dynamic role, you will lead the charge in innovation, contributing to the advancement of highly automated DNA sequencing pipelines and diagnostic applications. Your expertise will play a critical role in shaping the future landscape of genetic diagnostics. Roche is seeking a motivated and collaborative individual with strong analytical skills to join our team. As a Product Engineer, you will drive the development of high-quality devices, serving as a key player in the development and technology transfer of our prototype manufacturing process. This position entails close collaboration with internal and external hardware and software developers within the RSS team, as well as active engagement with the CD development team. | 3/5/2024 |
| 3114 | Roche Carlsbad, CA Process Engineer I - Night Shift Bachelor’s degree in Engineering or a related technical discipline. Exp: 1+ years |
The work schedule for this position is a night shift from Sunday through Friday from 10 PM to 6:30 AM. As a Process Engineer you are responsible for driving stable, reliable production processes. You are instrumental in troubleshooting, testing , and supporting for existing products and new product lines. Under minimal supervision, you will apply engineering principles to resolve complex manufacturing equipment issues that arise and implement initiatives to reduce equipment downtime and improve throughput yields. | 3/5/2024 |
| 3115 | Roche Carlsbad, CA Quality Control Specialist I - Mon-Fri 4:30 PM to 1 AM B.S. degree required, in basic sciences, life sciences, or engineering. Exp: 1 - 3 years |
This position conducts incoming, in-process and final release QC testing in a controlled manufacturing environment. This position may also execute validation studies, execute test protocols, analyze data, generate analytical reports, investigate Non-Conformances, evaluate processes & procedures, utilize statistical techniques, review specifications, and inspect & test equipment. May conduct training on quality related tools, methods, and procedures. Interfaces with R&D, Manufacturing, Quality, and Supply Chain within the company and when appropriate with customers and suppliers on quality related issues. | 3/5/2024 |
| 3116 | Roche Tucson, AZ IQC Technician II Bachelor's Degree preferred. Exp: < 1 year |
The Incoming Quality Control (IQC) Technician – Instruments Manufacturing, will be an integral part of a team that performs inspection of raw materials, components and sub-assemblies using established operation procedures, work instructions, engineering parts drawings. The individual will be responsible for the review, generation and sign-off of inspection reports and related quality documentation. The individual will be responsible for interfacing with highly complex systems and controls in an ISO 13485 and GMP manufacturing environment. The individual will maintain areas in high state of inspection preparedness by maintaining equipment, records and IQC environment in order to comply with regulatory requirements utilizing current regulations and Operating Procedures (OP). Additionally, maintains incoming inspection documents, assists in the investigation of incoming parts and instruments manufacturing non-conforming parts, manufacturing exception events and works independently with general guidance from senior team members. | 3/5/2024 |
| 3117 | RPRD Diagnostics Wauwatosa, WI Clinical Lab Technician I Bachelor's degree in genetics, biology, molecular biology, chemistry, biochemistry or related discipline. Exp: 1 year |
RPRD Diagnostics, LLC is seeking a Clinical Lab Technician I to join our team. At RPRD, we believe that comprehensive genetic testing offers an unprecedented opportunity to improve the outcomes for millions of patients who are prescribed drugs, so we are developing next-generation pharmacogenetics testing services to improve clinical decision making. We aim to enable hospitals, clinicians, and their patients to better understand and manage their treatment choices on the basis of each individual's unique genetic profile. Additionally, our team is committed to continuous innovation in order to advance knowledge and deliver cutting edge services and care to our clients and their patients. The Clinical Lab Technician I performs high complexity molecular techniques such as genotyping, next generation sequencing, data analysis and interpretation. They are further responsible for recognizing the clinical significance of each test performed, maintaining the confidential and sensitive nature of patient information and results, and reporting results within established time frames. This position also assists with the validation of new applications in the clinical laboratory and works collaboratively as part of a team to help ensure the smooth operation of the lab. | 3/5/2024 |
| 3118 | SAMDI Tech Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Sunday through Thursday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 3/5/2024 |
| 3119 | SAMDI Tech Worcester, MA Research Technician I - 2nd Shift Hours Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Monday through Friday 2nd shift hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 3/5/2024 |
| 3120 | SAMDI Tech Mattawan, MI Technician 1 - Histology, 2nd Shift Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred. Exp: 0+ months |
We are seeking an experienced Technician 1 - Histology for our 2nd Shift Pathology Services Team in Mattawan MI. A Technician 1 – Histology is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include handling tissues and organs, trimming tissues, embedding, measuring organ weights; microtomy, slide preparation, staining; inventory and quality control, and shipping of tissues. The technician is working under close supervision to gain proficiency. | 3/5/2024 |
| 3121 | SAMDI Tech Cambridge, MA Research Associate /Imaging Bachelor’s degree (B.A./B.S.) or equivalent in Animal Science or related field. Exp: One to two years |
We are seeking an Research Associate/ Imaging for our Insourcing Solutions Department based in Cambridge, MA. As the Research Associate/Imaging, you will perform multi-modality imaging studies, preclinical imaging data acquisition, image data processing and analysis, may also work with other scientists for in vivo and ex vivo imaging experiments. | 3/5/2024 |
| 3122 | SAMDI Tech Horsham, PA Formulations Technician I Bachelor’ degree (B.S.) preferred. Exp: 0 to 1 years |
Full Time – 40 Hours/Week $1000 SIGN ON BONUS (external applicants eligible only) Perform routine preparation of vehicles and test article dosage solutions for use in toxicology studies with close supervision. | 3/5/2024 |
| 3123 | SAMDI Tech Wayne, PA Technician I Molecular Biology Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 0-1 years |
Under direct supervision, responsible for performing daily laboratory tasks as they relate to Molecular Biology Testing Services. | 3/5/2024 |
| 3124 | SAMDI Tech Malvern, PA Technician I Microbiology Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 0-1 years |
Under direct supervision, responsible for performing daily laboratory tasks as they relate to Molecular Biology Testing Services. | 3/5/2024 |
| 3125 | Sanofi Pasteur Framingham, MA Purification Development Research Associate Bachelor's degree in Chemical Engineering, Biochemical Engineering, Biochemistry or related discipline Exp: 1+ years |
We are looking for candidates for the position of Research Associate. This individual will join a dynamic and motivated team to develop downstream purification processes in support of early and late stage drug development programs. In addition, the Research Associate will support the tech transfer of the developed process into the clinical manufacturing team or Industrial Affairs organization, while ensuring the highest standards of safety, environmental, and regulatory compliance are maintained in the workplace. | 3/5/2024 |
| 3126 | Sanofi Pasteur Swiftwater, PA Production Technician - Vaccine Associates or Bachelor’s Exp: AS: 1 + yrs; BS: 0 + yrs |
This is a third shift position. Must be able to work weekends and holidays as needed. Flexibility for changing schedule required. | 3/5/2024 |
| 3127 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science. Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 3/5/2024 |
| 3128 | SeaGen Groton, CT Associate Scientist, Sustainable Chemistry Data Bachelor’s Degree in Chemistry, Environmental Science or related field. Exp: 0 to 2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will become a member of Pfizer Chemical Research and Development (CRD) Sustainability Team, and will work under the guidance of the Sustainable Chemistry Lead. Your work alongside the entire department will help implement an overall strategy for the collection, analysis, management, and communication of sustainability related data and metrics. You will help execute the CRD Vision by measuring key sustainable metrics evolution over time as we commit to the development of greener processes to manufacture Pfizer APIs from clinical to commercial. Your role will support the company towards its goal of becoming Net Zero by 2040. You are able to work independently or within a small team under guidance from strategy leaders.Essential skills include excellent oral and written communication, proficient office computer software knowledge including data management (Microsoft Office, Spotfire) and teamwork-oriented mindset. Ideally, you have a solid knowledge of organic chemistry and you are passionate about data collection as well as sustainability. | 3/5/2024 |
| 3129 | SeaGen Bothell, WA Manufacturing QA Associate III Bachelors Degree Exp: 0+years |
You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe. | 3/5/2024 |
| 3130 | SeaGen Rocky Mount, NC Associate Validation Engineer Bachelors degree Exp: 0+years |
You will be a member of Pfizer’s dedicated and highly effective Validation team. You will be responsible for the creation, review and approval of validation master plan, SOPs, protocols and reports. Your methodological approach will help us ensure compliance of our quality systems with company standards and government regulatory requirements. Your problem-solving ability will help us troubleshoot validation problems for equipment and performance processes and conduct statistical analysis of testing results and process anomalies. Your documentation skills will guide the writing, review and approval of validation process documents and technical reports related to equipment, facilities, utilities, computer systems, products and processes. As an Associate Validation Engineer you will be responsible for validating/qualifying the systems, equipment, utilities used to manufacture and/or clean drug products within a large manufacturing facility located in North Carolina, USA. You will help to demonstrate systems are running according to necessary specifications and operate within regulations to ensure data integrity and the production of quality products. | 3/5/2024 |
| 3131 | SeaGen Kalamazoo, MI QC Laboratory Analyst II Bachelor’s degree in Chemistry, Biochemistry or related science. Exp: 0-1 years |
This position is for a testing analyst in the Kalamazoo QO API Non-LC Laboratory working on first shift. Opportunity for schedule flexibility exists as the Laboratory supports business and customer needs on weekends and holidays. Technologies employed in the API NonLC Laboratory include GC, Particle Size, X-Ray Crystallography, Karl Fisher, UV, and general analytical procedures. | 3/5/2024 |
| 3132 | Seracare Life Sciences Cumberland Foreside, ME Quality Control Technologist I Associates in Medical Laboratory Science or a Bachelor’s degree in Medical Technology (preferred) or related science degree (i.e. biology, chemistry, Exp: 1-3 years |
Follows standardized procedures and prepares samples for testing. Analyzes test results for accuracy, acceptability, and critical limits. Relies on limited independent judgment to plan and accomplish goals. Performs a variety of tasks. A limited degree of creativity and latitude is required. | 3/5/2024 |
| 3133 | Shionogi San Diego, CA Laboratory Assistant, Qpex BioPharma, wholly-owned subsidiary of Shionogi Inc. in San Diego, CA. Associates degree or a relevant certificate in a laboratory science field. Exp: 1+ years |
As a Lab Assistant you will play a vital role in supporting scientific and research activities within Qpex’s research laboratory. | 3/6/2024 |
| 3134 | Sigmapharm Laboratories Bensalem, PA Quality Assurance Associate At minimum, an associate’s degree in any life science. Exp: 1 to 3 years |
· Responsible for assisting the Head of Quality Assurance (QA) to ensure all pharmaceutical processes and documentation that may impact the safety, identity, strength, quality and purity of any drug product or drug substance manufactured at Sigmapharm Laboratories, LLC (Sigmapharm) complies with all applicable Standard Operating Procedures (SOPs) and regulatory requirements and is prepared or performed in a way that maintains quality and reduces potential risks. · Responsible for the review and approval of all product and process-related Official Documents. · Responsible for the review and approval of qualification related Documents such as protocols and reports. · Responsible for aiding in the control and organization of CGMP documentation, recorded information or data generated and maintained in document control. · Responsible for auditing batch records and overall operational procedures. | 3/6/2024 |
| 3135 | Smithers West Trenton, NJ Scientist (PCR and Molecular Biology) MS in Biological or Physical Sciences. Exp: 1-2 years |
Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance. PDS works with customers to develop new methods, validate existing methods, and perform the assays necessary to analyze samples from patients on more than 100 clinical trials. PDS is seeking a Scientist with experience in Molecular Biology to join our team. The successful candidate is able to apply prior experience and knowledge to successfully perform in a laboratory environment under regulated conditions. | 3/6/2024 |
| 3136 | Smithers Darien, IL Associate Chemist I - Smithers Cannabis Testing Services, Darien, IL BS degree in Chemistry or related field. Exp: 6 months |
Smithers Cannabis Testing Services is seeking an Associate Chemist I at our Darien, IL location. Job Summary The Associate Chemist I performs critical sample processing and extraction duties to prepare cannabis samples for analysis and enters sample information in the laboratory information management system (LIMS) to facilitate subsequent analysis. The position is responsible for maintenance of laboratory stock reagents. Operates and may maintain, under supervision, test equipment and apparatus. | 3/6/2024 |
| 3137 | Smithers Wareham, MA Assistant Biologist - Ecotoxicology - Smithers Wareham, MA Bachelors or better in Biology or related field. Exp: 0+ years |
Smithers Environmental Risk Sciences division is seeking an Assistant Biologist in the Ecotoxicology Department at our Wareham, MA location. Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. Incumbent will be introduced to mathematical and statistical procedures used to reduce and analyze study data. Responsible for maintaining cleanliness of the labs, storage and culture areas including maintenance and calibration of equipment used in any of these settings. May require routine involvement in seawater and/or sediment collection. Assignments are completed with minimal supervision. Assists with organization, direction and training of technicians. Assists in coordinating internal requirements for testing (i.e. chemistry support, Quality Assurance, reporting). Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations and company policies. | 3/6/2024 |
| 3138 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field. Exp: 6 months |
Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 3/6/2024 |
| 3139 | Smith and Nephew Pittsburgh or Andover, PA Software Engineer (Pittsburgh, PA or Andover, MA) Bachelor’s degree required (Software Engineering or Computer Science preferred). Exp: 0 - 2 years |
Software Engineer (Pittsburgh, PA or Andover, MA) Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living. The Software Engineer will be involved in research/design/testing of medical devices | 3/6/2024 |
| 3140 | Spherotech Lake Forest, IL Manufacturing Associate Bachelor's degree in Chemistry or related field. Exp: 0+ years |
Spherotech, Inc. seeks a college graduate for a Manufacturing Associate opening. Duties include polymer synthesis, bottling, packaging, documentation, etc. | 3/6/2024 |
| 3141 | Spherotech Lake Forest, IL Quality Control Associate Bachelor's degree in Chemistry or related field. Exp: 1 year |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. | 3/6/2024 |
| 3142 | Stability Biologics San Antonio, TX QA Specialist - San Antonio, TX BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.). Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 3/7/2024 |
| 3143 | StageBio Frederick, MD Laboratory Technician I/II/III · College degree preferred. Exp: 0+ years |
StageBio is seeking a full-time Laboratory Technician II to join our Frederick, Maryland facility. Primary Responsibilities Include: Individuals will be trained to perform tissue grossing, processing, embedding, microtomy, staining (H&E & special staining), quality control and general histology duties Maintain a safe working environment by following all safety and chemical regulations as outlined in StageBio’s SOPs Prompt and accurate recording of data Daily cleaning of work area and equipment Other duties assigned by management | 3/7/2024 |
| 3144 | Stellartech Research Milpitas, CA Quality Engineer II Typically requires a BS degree or equivalent. Exp: 1-3 years |
Stellartech is looking for a Quality Engineer to join our Team. | 3/7/2024 |
| 3145 | Tempus Durham, NC Molecular Technologist - Lead Trainer (Monday-Friday, 2:30pm-11:00pm) MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of said data. Here at Tempus, we believe the greatest promise for the detection and treatment of cancer lies in the deep understanding of molecular activity for disease initiation, progression, and efficacious treatment based on the discovery of unique biomarkers. We're on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. We're looking to build a laboratory team who are passionate and focused on developing state of the art techniques to processing and creating and interpreting vast amounts of genomic and molecular data. | 3/8/2024 |
| 3146 | Tempus Durham, NC Molecular Technologist - Lead Trainer (Monday-Friday, 8:00am-4:30pm) MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of said data. Here at Tempus, we believe the greatest promise for the detection and treatment of cancer lies in the deep understanding of molecular activity for disease initiation, progression, and efficacious treatment based on the discovery of unique biomarkers. We're on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. We're looking to build a laboratory team who are passionate and focused on developing state of the art techniques to processing and creating and interpreting vast amounts of genomic and molecular data. | 3/8/2024 |
| 3147 | NeoLight Scottsdale, AZ Biomedical Engineer Bachelor's Degree in Electrical Engineering (Required) from an accredited university or college. A Master's degree is preferred. Exp: entry-level or 1-2 years |
We seek a full-time entry-level Biomedical Engineer focusing on Electrical Engineering. In this role, you will provide strong, independent technical support to teams that contribute to resolving significant electrical and embedded system issues for the next generation and on-market products. A successful candidate will be a productive individual contributor who works independently with general supervision on larger, moderately complex projects/assignments. In addition, the candidate sets objectives for their job area to meet the objectives of projects and assignments. | 3/8/2024 |
| 3148 | TransMedics Andover, MA Mechanical Engineer I - Product Development BS in Mechanical Engineering, Plastics Engineering, Biomedical Engineering, or equivalent is required. Exp: 0-2 years |
Reporting to the Director of Mechanical Engineering, the Mechanical Engineer 1 will work with the cross- functional Product Development team to develop new products. The ideal candidate should be self- motivated and have a strong desire to learn and take on new responsibilities. The candidate will support larger programs under the mentorship of Sr. Staff and lead smaller projects with guidanace. The candidate will contribute to the full design process from concept to production. This position will have several opportunities to develop engineering skills including: CAD, technical analysis, technical writing, problem solving, engineering best practicices, and hand-on use of lab and machine shop equipment. | 3/8/2024 |
| 3149 | TransMedics Andover, MA Cardiothoracic Research Specialist Bachelor's degree in Biology, Biochemistry, Biomedical Sciences or related field. Exp: 1–2-year |
If you’re looking for a career with a company where you can make a difference, earn a competitive salary, and have ample professional growth opportunities, this is it. TransMedics is a publicly traded, medical technology company revolutionizing what’s possible in organ transplant through innovation, collaboration, and commitment. We’re growing and transforming the transplantation industry through our Organ Care System (OCS™) technology platform & National OCS Program, preserving organs used in heart, lung, and liver patienttransplants for safe transport nationwide. We are seeking a highly motivated and detail-oriented Cardiothoracic Research Specialist to joinour Cardiothoracic Research team. This position offers an excellent opportunity for an early career researcher to gain hands-on experience in cardiothoracic research while contributing tomeaningful projects within our dynamic research and lab environment. | 3/8/2024 |
| 3150 | Pharmaron San Diego, CA In Vivo Research Associate I, Ophthalmology Associates degree (preferred) in veterinary technology or BS. Exp: AS: 1-2 years; BS: 1 year |
Pharmaron (San Diego) is seeking to hire an outstanding candidate to join our Ocular department at the Research Associate I level. The Research Associate will play an important role by supporting in vivo studies to test devices being developed for various ocular disorders. | 2/27/2024 |
| 3151 | Pharmaceutics International Hunt Valley, MD Microbiologist (EM) B.S / M.S. in a life sciences discipline. Exp: 0-2 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions. | 2/27/2024 |
| 3152 | Phitonex Fremont, CA Scientist I, Formulations BS/BA in scientific field in Chemistry, Biochemistry, ore related technical discipline. Exp: 1+ years |
You will be responsible for manufacturing products for the Bulk Formulations Toxicology team and complete associated cGMP documentation. You will work with chemicals and biologicals to manufacture reagents, calibrators, and controls for IVD immunoassay use and participate in process improvements projects. | 2/27/2024 |
| 3153 | Phitonex Florence, SC Scientist I - Process R&D BS/BA degree in chemistry or life science. Exp: 0-3 years |
You will join a team of synthetic organic chemists in the manufacturing of pharmaceutical ingredients at the Florence, SC site. Many of our products are already in the market serving patients and we work on a variety of projects for existing and new clients. In this position, you will perform hands-on experimentation and learn knowledge and skills for the process development of pharmaceutical products. We have a fast-paced working environment while keeping a good work-and-life balance. | 2/27/2024 |
| 3154 | Phitonex Cincinnati, OH R&D/Mfg Scientist I (onsite) Associates or Bachelor’s Degree in physical science; Chemistry or Biology preferred. Exp: 1-2 years |
As a Quality Laboratory Team Member, you will coordinate with your supervisor and collaborate with colleagues in diverse groups to assure that critical timelines are met. You will have the opportunity to collaborate with your peers within the laboratory and those in other departments such as formulations, operations, project management and quality assurance on a regular basis. You will perform analytical methods for elaborate testing for validated and experimental methods and other tests as needed to support lab operations. You will participate in the validation of analytical test methods when additional resources are required. | 2/27/2024 |
| 3155 | Phitonex Middletown, VA Formulation Scientist I B.S. in Science or Medical Technology is preferred. Exp: 0+ years |
Work in a Value Stream environment and organize, carry out, monitor, multi-stage production processes to prepare and formulate serum, clinical diagnostic assays and reagents for use in research and commercial scientific products for the IVD industry with compliance to specifications and GMP/FDA requirements. The formulations range in scale from 1 mL to 50,000 L and are manufactured using protocols/batch records in an environmentally monitored lab space. Data is recorded in batch records following good documentation practices as required for regulated industries. | 2/27/2024 |
| 3156 | Plex Pharma San Diego, CA Research Associate, Biology & Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field. Exp: 1-3 years |
Plex Pharmaceuticals (www.plexpharma.com), a biotechnology company with a focus on developing novel drugs targeting misfolded and aggregated proteins, has an immediate opening for a Research Associate. The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 2/27/2024 |
| 3157 | Poochon Proteomics Solutions Frederick, MD Lab Assistant Associate degree or above in medical technology, or related life science is preferred. Exp: 1+ year |
We are seeking a Lab Technician to join our DNA Sequencing and Mass Spectrometry team. | 3/1/2024 |
| 3158 | PPD Middleton, WI Entry Level Biochemist Bachelor's degree or equivalent. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/1/2024 |
| 3159 | PPD Highland Heights, KY Assistant Scientist - 2nd Shift Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/1/2024 |
| 3160 | PPD Highland Heights, KY Assistant Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/1/2024 |
| 3161 | Prevail Therapeutics Boston, MA Associate Scientist, Early Preclinical Development - Inner Ear Biology Bachelor's Degree. Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 3/1/2024 |
| 3162 | Prevail Therapeutics San Francisco, CA Research Associate - DMPK DICE BS or MS in chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based Research Associate to join our Drug Metabolism and Pharmacokinetics (DMPK) team. This individual will be a key contributor to performing standard ADME/DMPK assays, such as microsomal stability, plasma protein binding, and metabolite identification. The individual will also be responsible for operating LC-MS instruments (QQQ and HRMS) with minimal direction. Do you have experience in mass spectrometry while doing enzyme related work? This role may be perfect for you! | 3/1/2024 |
| 3163 | Preventice Solutions Arden Hills, MN Quality Engineer I - Electrical Bachelor's degree or higher in Electrical Engineering. Exp: Entry-Level |
The Electrophysiology (EP) Design Quality Assurance team is looking for an engineer to evaluate manufacturing and design changes. EP has a broad portfolio of capital equipment used in the field to support ablation and diagnostic procedures. The EP Design Quality assurance team is growing, and the timely evaluation of design changes is key to maintaining a robust EP Capital Equipment portfolio to reduce potential safety and quality issues. This role provides visibility across the Research and Design organization. The selected candidate will collaborate with Manufacturing, Product Complaints, Regulatory, and Field Servicing engineering. This is a significant role for an entry-level engineer with opportunities to grow into Computer Programming, Cybersecurity, Risk, or Electrical Design. The selected candidate will be mentored by a Senior Electrical Engineer. | 3/1/2024 |
| 3164 | Preventice Solutions Maple Grove, MN Quality Engineer I University degree or the equivalent combination of education and experience required. Exp: 0-2 years |
Develops, establishes and maintains quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities. Provides focused quality engineering support within new product development, operational, or system/services support. | 3/1/2024 |
| 3165 | Procept BioRobotics San Jose, CA Electrical Engineer Bachelor's degree (B.S.) in Electrical Engineering or equivalent. Advanced degrees are a plus. Exp: 1-5 years |
The Electrical Engineer works within the Electrical Engineering group within the R&D Capital Equipment department. The position will be responsible for supporting electrical systems for PROCEPT’s electro-mechanical products, including electronics feasibility, requirements definition, design, design verification, test system development, manufacturing procedure development, and production transfer activities at various stages of the product development cycle. Development will be conducted in accordance with PROCEPT’s quality system. | 3/1/2024 |
| 3166 | ProteinSimple Minneapolis, MN Advanced Research Associate MS degree in the biological sciences. Exp: 0-2 years |
As an Advanced Research Associate you will work in the Immunocytochemistry Department on the validation of antibodies for immunocytochemistry applications. You will be knowledgeable of animal anatomy and histology and familiar with histological examination of tissues, frozen and paraffin-embedded tissue sections, immunohistochemistry protocols, microscopy systems; collect digital images, digital image post-processing and enter data into a database. | 3/1/2024 |
| 3167 | ProteinSimple Newark, CA Senior Research Associate, PAS MS in molecular biology, biochemistry, cell biology or related field. Exp: 0-2 years |
The Senior Research Associate (SRA) will serve as a key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic sponsors to detect RNA targets of interest. An additional critical work component will be the application of immunohistochemistry (IHC) to look for specific protein targets. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. It is expected that the Sr. Research Associate will independently collect and interpret data based on project expectations, which has implications for many downstream applications, such as biomarker validation and cell and gene therapy. The SRA will also be expected to independently utilize available resources for any required troubleshooting and communicate clearly with sponsors through both electronic mail and teleconference channels. The SRA must also coordinate with internal research and development (R&D) team to learn new techniques quickly and be able to adapt to shifting priorities in a fast- paced and growing start-up environment. | 3/1/2024 |
| 3168 | ProteinSimple Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of methylcellulose, methylcellulose-containing media, and stem cell and gene therapy (SCGT) media. Perform QC testing and analysis of some methylcellulose-containing media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Perform additional duties as assigned. Skills used include cell culture, high attention to detail, strong communication and organizational skills. | 3/1/2024 |
| 3169 | ProteinSimple Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of methylcellulose, methylcellulose-containing media, and stem cell and gene therapy (SCGT) media. Perform QC testing and analysis of some methylcellulose-containing media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Perform additional duties as assigned. Skills used include cell culture, high attention to detail, strong communication and organizational skills. | 3/1/2024 |
| 3170 | ProteinSimple Minneapolis, MN Research Associate Bachelor’s degree in a related field. Exp: up to 3 years |
Are you passionate about science, an adaptable self-starter with an insatiable curiosity and have a drive to innovate and further develop your skills with a multitude of analytical tools to study and characterize biomolecules? As a Research Associate in the Analytical Services team, you will be responsible for performing routine Quality Control (QC) testing, and participating in troubleshooting efforts for released products and new products that are still in development through the application of biophysical analysis of proteins and antibodies focusing on our capillary electrophoresis systems, but may also include chromatography, immunoassays, light scattering and other analytical tools, with the aid of fully defined SOPs. You will also actively take part in group projects, participate in process improvement efforts to improve lab protocols with the goal of facilitating innovation, efficiency and productivity, and perform additional duties as assigned. | 3/1/2024 |
| 3171 | ProteinSimple Minneapolis, MN Quality Assurance Specialist B.S degree in Biology related disciplines. Exp: 0 to 5 years |
The responsibilities of this position are to engage and support various improvement projects for Document Control (Label design and document writing, routing, approval etc) and Quality Assurance activities, including but not limited to Supplier Management, Non-Conformance, CAPA and Change Management etc. | 3/1/2024 |
| 3172 | ProteinSimple Minneapolis, MN Quality Technician, Hematology QC Lab MLT/MLS degree, bachelor’s degree in biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, basic troubleshooting, and operation of Hematology analyzers. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to set up and test product on all laboratory instruments and troubleshoot as necessary within 12 months of hire. This position will adhere to safety regulations. Understand the basic ISO protocols and other applicable standards. Perform additional duties as assigned. | 3/1/2024 |
| 3173 | QPS Newark, DE Associate Scientist II - Bioanalytical Dept Bachelor’s degree. Exp: 1-2 years |
As an Associate Scientist II in our Bioanalytical department, you will be a fully supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. | 3/1/2024 |
| 3174 | QPS Newark, DE Associate Scientist I - TLM Bachelor’s Degree Biology, Molecular Biology, Biochemistry, Immunology, Pharmacology, Medical Technology, or a related field. Exp: 0+ years |
Perform routine lab operations, such as preparing reagents, pipetting, weighing, monitoring, recording, and replenishing supplies Assist supervisor in performing analysis of drug or other targets in complex biologic matrices Set-up, use and maintain complex instrumentation Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Perform routine mathematical & chemical calculations | 3/1/2024 |
| 3175 | Quanterix Billerica, MA Manufacturing Associate I BS in Chemistry, Biology or related Life Sciences. Exp: 0+ years |
We are looking for an experienced and highly motivated Manufacturing Associate I located in Billerica, MA to join our Planar Manufacturing team. individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. Hours for this position are 8am-4:30pm. | 3/1/2024 |
| 3176 | Quidel Rochester, NY Scientist I, Quality Labs BS degree in scientific or related field. Exp: 0 to 2 years |
As we continue to grow as QuidelOrtho, we are seeking a Scientist I in the Reference Laboratory. The Scientist I assures the Calibration Traceability by executing complex analytical testing of patient samples and other fluids to support the release process, stability testing, accuracy testing, and new method development. This testing uses a variety of instrumentation including, but not limited to, pH meter, manual spectrophotometers, Olympus AU400, Beckman AU480, flame photometers, atomic absorption, RIA, and HPLC. The Scientist I will maintain instrumentation, calibrates, runs quality control and analyzes requested samples. Position requires summary reports, analysis of technical data, evaluation of quality control, and instrument troubleshooting. Completion of Non-Conformance Records and/or Quality Investigations in a timely manner is required for this position. Work is scheduled, supervised, and follows established methods and procedures. Business decisions and product accuracy is dependent upon the technical ability of this individual and reproducibility of the analytical methods. This position is located on-site in Rochester, New York. | 3/1/2024 |
| 3177 | Quidel Rochester, NY Quality Analyst I (Fluid Release / Microbiology) Bachelor’s degree in Microbiology, Biology, Medical Technology, Biochemistry. Exp: 1+ years |
As we continue to grow, we are seeking Quality Analyst I to execute complex analytical testing of VITROS Calibrators, Control and other product fluids to support the formulation, release process, stability testing and accuracy of the VITROS products. This testing uses a variety of instrumentation including, but not limited to, VITROS 5,1 Chemistry System, pH meter, Chloride meter, conductivity meter and manual spectrophotometers. Will maintain VITROS instrumentation, calibrates, run quality control and analyze requested samples. In addition to support as a floater the Microbiology Laboratory testing. Works under the guidance of senior laboratory staff and management to resolve routine to complex analytical quality issues, assist in laboratory investigations and assures the product performance meets specification and claims. This position is located in Rochester, NY. | 3/1/2024 |
| 3178 | Quidel Athens, OH QC Technician II Bachelor’s degree in Chemistry, Biology, Life Science or similar discipline. Exp: 1-3 years |
The Quality Control Technician II is primarily responsible for performing Quality Control testing products at various stages of Production, as well as occasional basic technical tasks such as document control, maintenance of work areas and may perform inventory control. The QC Technician II will be expected to maintain proficiency in all areas such that re-assignment will be seamless when there are changes to workload and/or company focus. This role is located in Athens, Ohio. | 3/1/2024 |
| 3179 | Reckitt Benckiser Pharmaceutical Montvale, NJ R&D Microbiology Lab Scientist/Assistant, Equity, Claims, Compliance Bachelors Degree in a Biological Science (with microbiology focus preferred). Exp: 6 months to 2 years. |
• Conduct disinfection and sanitization efficacy tests (e.g. AOAC, ASTM, CEN,) to evaluate the antimicrobial efficacy of experimental formulations, finished products and ingredients. • Conduct required stability tests (preservative challenge tests, microbial limits) for personal care product development and launch support. • Help create new microbiological methods to foster a pipeline of innovative claims. • Manage multiple projects and provide microbiological support within the required project timelines (including testing and reporting of results) to various project teams. • Act as a subject matter expert in Microbiology. • Work with external partners in a professional and productive manner. • Perform appropriate laboratory practices and procedures, and consistently maintain laboratory records and notebooks in compliance with Good Laboratory Practice standards. • Review/author existing laboratory Standard Operating Procedures and apply them to lab and testing responsibilities. • A solid understanding of microbiology and techniques used for isolating, growing and identifying bacteria. Propagation and maintenance of appropriate microbial stocks. | 3/1/2024 |
| 3180 | Reckitt Benckiser Pharmaceutical Montvale, NJ R&D Assistant, Chemistry and Measurement Sciences- Analytical BS/BA in Chemistry or related field. Exp: 0-2 years |
Reckitt Research and Development CMS (Montvale, NJ) is seeking a self-motivated analytical chemist to join our team in the role of Assistant in the Analytical lab. The successful candidate would work independently with supervision in the lab, supporting analytical measurement for Health & Hygiene global new product development, including the Lysol, Dettol, and Harpic brands. | 3/1/2024 |
| 3181 | Reaction Biology Malvern, PA Research Associate I Bachelor of science degree. Exp: 1+ years |
To provide ground level lab work following standard protocols according to department needs. The employee will support other team members in the execution of routine lab procedures, as well as to help sustain the functionality of the lab through regular cleaning, stocking inventory, and maintenance. | 3/1/2024 |
| 3182 | Reata Pharmaceuticals Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred) OR BioWork Certificate or Associate’s Degree. Exp: 1+ years |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 3/1/2024 |
| 3183 | Reata Pharmaceuticals Research Triangle Park, NC Associate II, QA - Swing Shift Bachelor’s degree preferably in a field of science or biotechnology. Exp: 0-2 years |
The Quality Assurance Associate II is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. Activities include but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identifying gaps in existing Quality systems and proposing solutions to site management. The QA Associate will perform all duties in a manner consistent with site and corporate policies, cGMP, safety, environmental and human resources policies and procedures and also adhere to all regulatory licenses and regulations, interfacing with key Quality and manufacturing customers, and coordination of investigations impacting the RTP site. The QA Associate may participate in internal compliance audits; assess and approve discrepancies from site, corporate, and regulatory guidance. The QA Associate will also ensure compliance with training policies. Please note that this is a Swing Shift position and will work a traditional 2-2-3 Manufacturing Rotation from 12pm to 12am, on a 12hr/shift schedule. There is a 10% pay differential for this position. | 3/1/2024 |
| 3184 | Reata Pharmaceuticals Research Triangle Park, NC Associate II, Quality Assurance Bachelor’s degree preferably in a field of science or biotechnology. Exp: 0-2 years |
The Associate II, Quality Assurance is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. Activities include but are not limited to review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identify gaps in existing Quality systems and propose solutions to site management. | 3/1/2024 |
| 3185 | R&D Systems Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 year |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 3/1/2024 |
| 3186 | R&D Systems Wallingford, CT Research Associate, Reagent Manufacturing Bachelors’ Degree in Biology, Chemistry, Biochemistry or related biological science. Exp: 1+ years |
The candidate will be responsible for providing accurate, efficient and quality production tasks in a cutting-edge molecular biology laboratory. The individual must exhibit a high degree of attention to detail and follow multi-step complicated technical protocols and processes accurately and rapidly. A basic molecular biology or biochemistry laboratory skill set is required as is experience in the use and maintenance of multiple types of biological instrumentation and systems. This position requires the ability to function with minimal oversight and convert customer demands into finished product. The individual will execute production protocols and ensure continual operation of equipment to meet production targets assigned by management, effectively and immediately communicate any complications that arise during manufacturing, and then be able to work across teams to establish and maintain a solution and provide detailed documentation of manufacturing activities, on a daily basis. | 3/1/2024 |
| 3187 | R&D Systems Minneapolis, MN Senior Manufacturing Technician Bachelor’s Degree in Science or Engineering. Exp: 1+ years |
The responsibilities of this position are to organize and stage different types of vials and bottles for filling. The position requires that the candidate has the ability to fill antibodies and protein solutions into vials. The candidate may be required to perform calculations based on volume and purity. The candidate must have the ability to cap and label vials of antibodies and proteins quickly and accurately. The candidate will be required to complete computer inventory entries and track supplies accurately. The candidate must have the ability to work in a laminar flow hood and fill (pipetting) products for extended periods of time. The candidate must have the ability to inspect vials with product and identify defects. The candidate will be required to operate cap torqueing and labeling automation. The candidate's ability to trouble shoot automation is an added skill set that would be desirable. The candidate will be required to learn nationalization process. The candidates' ability to complete paperwork accurately is critical. The candidate's ability to work in a fast-paced regulatory environment as a team is critical. The candidate must have the ability to gown and work in a clean room. The candidate performs pipette calibration accurately. The candidate may work on new production introduction, implementation, and filling. The candidate will help with yearend inventory counting and perform additional duties as assigned. The candidate will be required to exhibit EPIC behaviors aligned with the corporate vision. | 3/1/2024 |
| 3188 | R&D Systems Minneapolis, MN Advanced Research Associate Master’s degree. Exp: 1+ years |
In this role, you would be responsible for the development and execution of QC test method validations for a variety of products, utilizing a wide variety of laboratory techniques such as cell culture, flow cytometry, qPCR, and other analytical methods. This position also assists in troubleshooting investigations and process improvement projects. As an Advanced Research Associate, you will also participate in cross-functional teams focused on new product introduction. | 3/1/2024 |
| 3189 | Roche Seattle, WA Lab Assistant BS in Chemistry, Biochemistry, Biology or related field. Exp: 1+ years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its novel Sequencing by eXpansion (SBX™) technology. SBX™ uses unique applications from chemistry, biochemistry, and protein engineering to sequence DNA by nanopore in rapid time with high accuracy and low cost. We are looking for people who are excited to collaborate with us to make SBX successful. You will join the SBX Central Services team of Lab Assistants and play a crucial role in the day-to-day operations of the lab. | 3/1/2024 |
| 3190 | Nexus Pharmaceuticals Lincolnshire, IL Quality Control Chemist I BS or MS in chemistry or related field with a minimum of 20 hours of chemistry coursework. Exp: one year |
The Quality Control Chemist I is responsible for the execution of wet chemistry and analytical chemistry techniques during testing of Raw Materials and finished products. This testing includes: Instrumental analysis such as HPLC, GC, UV and FTIR as well as wet chemistry such as titrations, LOD and chemical identification tests. The Quality Control Chemist I performs method development or method transfer testing. The Quality Control Chemist I works in the laboratory in a safe and effective manner. | 2/20/2024 |
| 3191 | Nostrum Laboratories Bryan, OH Chemist I Bachelors Degree. Exp: 0 - 4 years |
Responsible for development and validation of analytical methods in support of product development and IND/NDA/ANDA filings. Perform routine wet chemical and instrumental analysis on raw materials, in-process, finished and stability products. Accurately compiles and reports data. Gather, compile and compose documents needed for regulatory submissions. | 2/20/2024 |
| 3192 | Nostrum Laboratories Bryan, OH QC LAB TECHNICIAN I Associates Degree. Exp: 1-2 years |
The QC Technician I is responsible for conducting non-complex analytical tests for raw materials, components, in-process materials, finished products, other samples as assigned, in accordance with cGMP regulations, regulatory filings, and approved procedures. | 2/20/2024 |
| 3193 | Novartis Cambridge, MA Research Scientist II, Cell Pharmacology – CVM MS degree in biochemistry, molecular or cell biology, biophysics, biomedical engineering or a related field. Exp: 0+ years |
We are seeking a highly motivated Research Scientist II to join our Cell Pharmacology team. You will advance our understanding of disease biology, contribute to target identification efforts, and work towards the discovery and optimization of new drugs for The Cardiovascular and Metabolic Disease Area (CVM) of Biomedical Research. The work involves collaboration with research scientists across multiple disciplines as well as translational medicine colleagues who support bringing our drugs to patients. | 2/22/2024 |
| 3194 | Novartis San Diego, CA Research Scientist II, CGT Biodistribution and Technology Scientific background with an BS in Biological Sciences or a closely related discipline. Masters preferred. Exp: 1+ years |
We are seeking a highly motivated scientist to contribute to gene therapy development as part of the global community of investigators in the Cell & Gene Therapy (CGT) group within BRC. The successful candidate will work at the cutting edge of gene therapy biodistribution, platform and technology research to model and test priorities in translational research. The successful candidate will be a collaborative scientist experienced in molecular biology experiments, liquid handling automation and/or NGS sequencing. | 2/22/2024 |
| 3195 | Novartis Emeryville, CA Research Scientist, Comparative Medicine Bachelor’s degree (B.A./B.S.) in animal or life sciences field preferred. Exp: 1+ years |
Comparative Medicine (CM) provides high quality husbandry and in vivo research work and support to enable drug discovery research and development. We are looking for a Research Scientist in CM to provide husbandry and vivarium Operations support, and to help run in vivo research studies and projects to support the diverse and exciting project portfolio at GH. The candidate should be action-oriented, Experienced with rodent husbandry and vivarium operations, skilled in in vivo procedures used to perform in vivo experiments with high technical and ethical standards and provide best in class animal care. The role will require an ability to work independently as well as in close collaboration with other CM colleagues, research scientists, the IACUC and animal welfare team. | 2/22/2024 |
| 3196 | Novartis Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 7am - 5:30pm) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 2/22/2024 |
| 3197 | Novartis Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 2:30pm - 1:00am) BA or MS in chemistry, biochemistry, microbiology, or other related science Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 2/22/2024 |
| 3198 | Novo Nordisk Durham, NC Manufacturing Operator I - Future 2nd Shift Associate’s degree preferred. Exp: one (1) year |
Efficiently, effectively & safely clean, setup & operate manufacturing equipment to achieve production goals, while adhering to applicable cGMPs & SOPs. | 2/22/2024 |
| 3199 | Novo Nordisk West Lebanon, NH Manufacturing Science and Analytical Technology Associate I Bachelor’s degree or equivalent in Biochemistry, Chemistry, Engineering or a closely related field. Exp: one year |
This position has the responsibility of working with senior level Scientists to execute laboratory scale process development or validation studies in support of process or assay development, or process troubleshooting or scale-up. The scientific knowledge in this position will range from familiarity with details of manufacturing process, process chemistries, development studies and relevant assay methods and instruments. This position will be one of the interfaces between MSAT and Manufacturing or Quality. | 2/22/2024 |
| 3200 | Novo Nordisk Clayton, NC Associate Process Engineer - FP - TECH SUPPORT - Assembly - Nights - Team C Bachelor’s degree in Chemical Engineer, Mechanical Engineering, or related discipline. Exp: One (1) year |
Responsible for assisting with design and implementation of manufacturing processes, instrumentation and equipment start-ups from the laboratory through manufacturing scale. | 2/22/2024 |
| 3201 | Novo Nordisk West Lebanon, NH Manufacturing Technician- Night Shift Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 2/22/2024 |
| 3202 | Novo Nordisk Durham, NC Maintenance Technician I - 2nd Shift AA/AS/AAS degree from an accredited university in a relevant field required. Exp: one (1) year |
Improve systems & equipment reliability on assigned process, reduce system/equipment downtime on assigned process & support operation of assigned process. | 2/22/2024 |
| 3203 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 2/22/2024 |
| 3204 | NxStage Ogden, UT Biocompatibility Engineer I Bachelor's Degree in related Engineering or scientific discipline required. Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 2/23/2024 |
| 3205 | NxStage Southaven, MS Medical Lab Scientist - Microbiology Bachelor's Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 - 3 years' |
Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 2/23/2024 |
| 3206 | NxStage Rockleigh, NJ Medical Lab Scientist - Diagnostic Immunology Bachelor’s Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 – 3 years’ |
Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 2/23/2024 |
| 3207 | NxStage Southaven, MS Medical Lab Scientist - Hematology Bachelor’s Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 – 3 years’ |
Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 2/23/2024 |
| 3208 | NxStage Mesa, AZ Biomedical Equipment Technician Associate Degree in electronics / biomedical technology, or equivalent a plus. Exp: 0 – 1 year |
Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and consistent with completed training and qualifications, schedules and performs routine repair and maintenance activities of medical equipment, water systems and the physical plant in assigned facilities that ensures patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer’s documentation, industry standards and local, state and federal regulatory requirements. Responsible for efficient use of resources related to repair and maintenance costs. | 2/23/2024 |
| 3209 | NxStage Richmond, VA Biomedical Equipment Technician Associate Degree in electronics / biomedical technology, or equivalent a plus. Exp: 0 – 1 year |
Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and consistent with completed training and qualifications, schedules and performs routine repair and maintenance activities of medical equipment, water systems and the physical plant in assigned facilities that ensures patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer’s documentation, industry standards and local, state and federal regulatory requirements. Responsible for efficient use of resources related to repair and maintenance costs. | 2/23/2024 |
| 3210 | NxStage Saint Peters, MO Biomedical Equipment Technician Associate Degree in electronics / biomedical technology, or equivalent a plus. Exp: 0 – 1 year |
Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and consistent with completed training and qualifications, schedules and performs routine repair and maintenance activities of medical equipment, water systems and the physical plant in assigned facilities that ensures patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer’s documentation, industry standards and local, state and federal regulatory requirements. Responsible for efficient use of resources related to repair and maintenance costs. | 2/23/2024 |
| 3211 | Ocean Ridge Biosciences Exton, PA Lab Assistant Associate or bachelor’s degree preferred. Exp: 1+ years |
The Lab Assistant will work under the supervision of laboratory staff or researchers to assist in the smooth functioning of laboratory operations. This role involves a combination of technical and administrative tasks to support ongoing laboratory activities and required documentation. Additionally, the Lab Assistant will provide crucial support for clinical trial kitting activities and sample receipt. | 2/23/2024 |
| 3212 | Ocean Ridge Biosciences Chicago, IL Assistant/Associate Toxicologist BS degree in animal/veterinary science, biology, or related disciplines. Exp: Assoc: 0-3 years |
The Associate/Assistant Toxicologist plays a key, hands on role in the conduct of preclinical studies and supports the Study Director to ensure that Sponsor studies are conducted properly and according to FDA guidelines. | 2/23/2024 |
| 3213 | Ocean Ridge Biosciences Hayward, CA Research Associate M.S. degree in related scientific discipline. Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 2/23/2024 |
| 3214 | Ocean Ridge Biosciences Exton, PA Associate Scientist/Scientist Scientist: M.S.; Associate Scientist: B.S./B.A. Exp: Scientist: 1-5 years; Associate Scientist: 1-5 years |
This is a technical scientific position within the Biologics Service Team. The Biologics Service Team is responsible for conducting bioanalytical methods related to large molecule biotherapeutic drug development across all therapeutic areas, spanning nonclinical studies to post-market clinical development. | 2/23/2024 |
| 3215 | Ocean Ridge Biosciences Exton, PA Lab Technician High School diploma, associate degree, or bachelor’s degree. Exp: 0-2+ years |
Frontage Laboratories, Inc. is hiring a Laboratory Technician I/II in the CMC Analytical Services division. The Laboratory Technician is responsible for supporting scientists in laboratory testing activities. The Laboratory Technician’s duties include following procedures, recording data, working with laboratory equipment, ordering supplies, and maintaining an inspection ready work environment. | 2/23/2024 |
| 3216 | Ocean Ridge Biosciences Exton, PA Lab Technician Bachelor’s degree in molecular biology, Biology, Biochemistry, Chemical Engineering, Mechanical Engineering, or equivalent. Exp: 1-5 years |
We are looking for a qualified Lab Technician to join our team. The role will perform and support laboratory procedures and controls within Biologics, Gene, and Cell Therapy (BGC) Department to maintain efficiency and compliance for the laboratory. The ideal candidate needs to have an entrepreneurial spirit that enables her/him to wear multiple hats as we scale-up the laboratory business. The candidate will have experience in working in a laboratory environment, preferably within biologics/or GCT lab. The candidate will be well-trained to maintain safety conditions in the lab and expected to be passionate in working in a matrix organization environment. The goal is to optimize lab compliance and maintaining the smooth running of the lab. | 2/23/2024 |
| 3217 | Ocean Ridge Biosciences Exton, PA Associate Scientist Bachelor’s or master’s degree in molecular biology, cell biology, biochemistry, or a related field. Exp: 1+ years |
The Cell-based Assay Core Lab, based at our Exton headquarters, stands as a premier provider of diverse cell-based assays. These include potency assays, neutralizing antibodies assays, EliSpot, virus plaque assay, TCID50 Assays etc. We are seeking a candidate with a fundamental understanding of Cell Biology, Biochemistry, and Molecular Biology. The ideal candidate should be highly organized, self-motivated, enthusiastic about learning, and capable of managing multiple projects concurrently | 2/23/2024 |
| 3218 | Ocular Therapeutix Bedford, MA Manufacturing Operator Associate degree or biotechnology certificate strongly preferred. Exp: 1-3 years |
The Manufacturing Operator is responsible for performing all manufacturing processes related to the Ocular Therapeutix’s products. The Operator is an integral part of our team and will be responsible for manufacturing activities by following appropriate SOP(s) and supervisor direction, in accordance with current good manufacturing practices and company policy and procedures. | 2/23/2024 |
| 3219 | Ocular Therapeutix Bedford, MA Device Engineer I Bachelor’s degree (in Mechanical Engineering, Biomedical Engineering or related discipline. Exp: 0 - 2 yrs |
We are seeking a motivated engineer to join the Product Development team. The individual is responsible for contributing to the design and manufacture of injectors and applicators used for the delivery of hydrogel drug product to treat various ophthalmic conditions. Responsibilities include product design (CAD modeling), design verification, design validation and other elements of Design Control. The role also includes process development activities, line layout, fixture design, equipment procurement, and supporting GMP manufacturing of clinical trial material. This individual will participate in defining voice of the customer requirements and product and material specifications. They will also perform risk analysis activities and design verification testing. This role will require a mix of cross-functional collaboration as well as execution of key laboratory experiments to achieve program objectives. The position is set in a dynamic and fast-paced environment. Critical areas of immediate focus include planning and execution of laboratory experiments, CAD design and maintenance of engineering drawings, Design for Manufacturability, process development and incorporation of fixture design and semi-automated processes to support development of manufacturing processes for late-stage clinical production that are capable, scalable, and sufficiently robust for transfer to commercial manufacturing. We are seeking a motivated engineer to join the Product Development team. The individual is responsible for contributing to the design and manufacture of injectors and applicators used for the delivery of hydrogel drug product to treat various ophthalmic conditions. Responsibilities include product design (CAD modeling), design verification, design validation and other elements of Design Control. The role also includes pr | 2/23/2024 |
| 3220 | OriGen Biomedical Austin, TX Manufacturing Engineer I Bachelor’s degree in Engineering. Exp: 0-2 years’ |
The Manufacturing Engineer I will evaluate and develop processes to ensure quality, cost, and efficiency requirements are met. S/he will troubleshoot problems with production and take corrective actions and will research and make recommendations on the purchase of equipment and/or upgrades to existing equipment and support manufacturing as needed. | 2/23/2024 |
| 3221 | Parexel West Point , PA Scientist II - Microbiologist Bachelor’s degree required; concentration in a scientific or applied discipline strongly preferred. Exp: 1-2 years |
We are looking to fill a Scientist 2 position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. | 2/23/2024 |
| 3222 | Parexel Rahway, NJ Scientist 3 - Drug Product Microbiologist Bachelor’s degree required; concentration in a scientific or applied discipline strongly preferred. Exp: 1-2 years |
We are looking to fill a microbiologist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in Rahway, NJ. | 2/23/2024 |
| 3223 | Parexel Rahway, NJ Crystallization Engineer III MS degree or equivalent in Engineering, Chemistry, Chemical Engineering, or a related field is required. Exp: 1-2 years’ |
We are looking to fill an Engineer 3 position working as a full-time employee of Parexel on long-term assignment onsite at one of our clients in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. Overview / Responsibilities The Chemical Engineering Research and Development department of one of our clients in Rahway, NJ has a position available that will have primary accountability for lab process development specifically around API crystallization, isolation, drying, and particle physical attribute control. Activities will include working with gram quantities at the bench scale to a few kilograms at the Unit Operations and Preplab scales utilizing wet and dry processing equipment within these labs (e.g., crystallization vessels, filtration and drying equipment, and wet and dry milling tools, etc.). The department offers fast-paced, hands-on research that requires a high degree of technical skills and contributions. Secondary activities may include experiments and the use of instruments associated with process safety evaluation when needed, and the general support of Specialty Labs operations within the Chemical Engineering R&D Department. | 2/23/2024 |
| 3224 | Par Pharmaceutical Rochester, MI Microbiologist I Bachelor of Science degree in microbiology, biology or related field with microbiology coursework required. Exp: 1+ years |
Performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 2/23/2024 |
| 3225 | Par Pharmaceutical Horsham, PA Associate Scientist, Bioprocess Technical Operations Bachelor’s degree in a biological, chemical, or related discipline is required. Exp: 1+ years |
The Associate Scientist will perform lab duties under the direct supervision of senior Biotech Ops (BTO) staff. Key areas of focus/support include preparation of buffers as well as execution of one or two specific methods or processes. | 2/23/2024 |
| 3226 | Par Pharmaceutical Rochester, MI Quality Associate Specialist, Product Release (Afternoon Shift) BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 2/23/2024 |
| 3227 | Partner Therapeutics Lynnwood, WA Quality Control Lab Support Technician I (Contract/Onsite) B.S. or equivalent degree in science (Biology, Chemistry, Biochemistry, etc.) or related field (Chemical Engineering, etc.) strongly preferred. Exp: 1 year |
The Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine which includes testing raw materials, process intermediates, Bulk Drug Substance (“BDS”), and Drug Product (“DP”). The Lab Support Technician I role is an individual contributor who maintains and prepares the onsite laboratories to perform required testing. This position is an ONSITE role requiring a presence 5 days per week at our Lynnwood, WA plant which is a cGMP production scale manufacturing facility for our product, Leukine® (sargramostim), a therapeutic glycoprotein. | 2/23/2024 |
| 3228 | Partner Therapeutics Lynnwood, WA Quality Control Lab Support Technician I (Onsite) B.S. or equivalent degree in science (Biology, Chemistry, Biochemistry, etc.) or related field (Chemical Engineering, etc.) strongly preferred. Exp: 1 year |
The Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine which includes testing raw materials, process intermediates, Bulk Drug Substance (“BDS”), and Drug Product (“DP”). The Lab Support Technician I role is an individual contributor who maintains and prepares the onsite laboratories to perform required testing. This position is an ONSITE role requiring a presence 5 days per week at our Lynnwood, WA plant which is a cGMP production scale manufacturing facility for our product, Leukine® (sargramostim), a therapeutic glycoprotein. | 2/23/2024 |
| 3229 | PeproTech St. Louis, MO Lab Technician II-Formulations Associate’s degree in science field or or Bachelor’s degree in science or engineering field. Exp: AS: 1+ years; BS: 0+ years |
The candidate will be responsible for the performance of operations in support of the BPS Cell Culture Development Team. You will carry out a variety of functions related to Upstream Process Development operations with primary focus on medium and buffer formulations. Additional functions may include but are not limited to activities such as supply stocking and organization, and equipment maintenance including basic troubleshooting, cleaning, and performance maintenance on supporting equipment. | 2/23/2024 |
| 3230 | Merieux NutriSciences Minnetonka, MN Microbiology Lab Tech Associate's degree in STEM degree preferred. Exp: 1+ year |
We are looking for a Microbiology Lab Tech in 11585 K-Tel Dr, Minnetonka, MN 55343 USA. Your mission will be to: Purpose (Objective): The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. | 2/12/2024 |
| 3231 | Merieux NutriSciences Stone Mountain, GA Microbiology Laboratory Technician Associates degree or equivalent work experience. Exp: 1+ year |
We are looking for a Microbiology Laboratory Technician in 2169 West Park Court, Stone Mountain, GA 30087 USA. Your mission will be to: Purpose (Objective):The incumbent prepares samples for processing and maintains documentation of process to facilitate testing procedures. | 2/12/2024 |
| 3232 | Merieux NutriSciences Salt Lake City, UT Chemistry Technician Associates degree or Bachelors degree. Exp: AS: 1+ years; BS: 0+ years |
We are looking for a Chemistry Technician in 1945 Fremont Drive, Salt Lake City, UT 84104 USA. Your mission will be to: Composting and grinding of samples for analysis as required. Perform chemical analyses such as protein, moisture, fat, ash, and other components. Prepare sample for analysis according to procedure. Retrieve samples from designated areas (e.g. log-in, sample storage). Perform chemical analyses of macronutrients, micronutrients or other parameters as designated. Extract desired component from sample with appropriate processes so that concentration can be determined. Prepare standards and reagents that are needed for the analysis procedure. Write/label all samples throughout the process so that Client and sample numbers can be tracked. Perform calculations, checking and interpretation of results where applicable. Track status of designated tests as assigned to ensure Client turn around time commitments are met and inform supervisor of non compliance. Assist other departmental personnel with analysis tasks so that testing can proceed according to specified time limits. | 2/12/2024 |
| 3233 | Merieux NutriSciences Minnetonka, MN Media Technician Associate's degree in STEM degree preferred. Exp: 1+ years |
We are looking for a Media Technician in 11585 K-Tel Dr, Minnetonka, MN 55343 USA. Your mission will be to: Purpose (Objective): The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. | 2/12/2024 |
| 3234 | Merieux NutriSciences Springfield, MO Microbiologist I Associates degree required, Bachelors preferred or equivalent work experience. Exp: One (1)- 2 years |
We are looking for a Microbiologist I in 2835 N Oak Grove, Springfield, MO 65803 USA. Your mission will be to: Purpose (Objective): The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. Schedule is 11:30-8p, Tuesday-Saturday. | 2/12/2024 |
| 3235 | Merieux NutriSciences Crete, IL Microbiologist III Masters degree. Exp: 1-2 years |
We are looking for a Microbiologist III in 3600 Eagle Nest Dr, North Building, Crete, IL 60417 USA. Your mission will be to: The incumbent is responsible for the testing of food samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 2/12/2024 |
| 3236 | Merieux NutriSciences Gainesville, FL Microbiology Lab Technician Associates degree. Exp: 0+ years |
We are looking for a Microbiology Lab Technician in 2183 SE Hawthorne Rd, Gainesville, FL 32641 USA. Purpose (Objective):The incumbent prepares samples for processing and maintains documentation of process to facilitate testing procedures. | 2/12/2024 |
| 3237 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1+ years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. | 2/12/2024 |
| 3238 | Meso Scale Discovery Rockville, MD Product Transfer Associate I Bachelor degree in Biology, Chemistry, Biotechnology, Engineering or related field, or associate’s degree with equivalent experience. Exp: One year |
This position is responsible for manufacturing assay kit components during development phases, meeting production schedules and troubleshooting. The role is cross-disciplinary and requires coordination across multiple departments (Operations, Quality, Research & Development, etc). | 2/12/2024 |
| 3239 | Microbiologics Saint Cloud, MN Quality Control Technician Four-year microbiology or related degree required. Exp: 1+ years |
We are currently looking to add a Quality Control Lab Technician to our St. Cloud, MN team. In this role, you will perform Quality Control Testing, Shelf-Life Testing, and Packaging Event Evaluations on Microbiologics products in accordance with the appropriate Company Device Master Record (DMR), policies and procedures with the objective to release only production products that meet all of Microbiologics acceptance criteria. | 2/12/2024 |
| 3240 | Microbiologics Lexington, KY Microbial Production Technician Bachelor’s degree in Biology, Microbiology or closely related field. Exp: 0+ years |
We are currently looking to add a Microbial Production Technician to our team in Lexington, KY. In this role, you will be responsible for manufacturing of microorganism product line, fungal serology, proficiency materials, and custom and retail products, in addition to other duties listed below. | 2/12/2024 |
| 3241 | Microbiologics Saint Cloud, MN Research & Development Technician Four (4) year degree in relevant field (e.g., biology, microbiology, virology, cell biology molecular biology). Exp: 1+ years |
We are currently looking to add a R&D Technician to our team in Research & Development. In this role you will be responsible for assisting with supervised experiments using microbiology and molecular biology techniques and/or cell culture and virology techniques as well as other applicable methodologies leading to new products or process improvements. | 2/12/2024 |
| 3242 | Mirati Therapeutics Summit West, NJ Specialist, QA Engineering Bachelor of Science degree required. Exp: 1 year |
The Specialist is responsible for providing quality oversight for Site Validation activities and Quality Control Laboratory method and equipment validation in accordance with BMS policies, standards, procedures and Global cGMP. Functional responsibilities for the incumbent include ensuring accurate and timely maintenance and review of validation and qualification documents for all equipment, laboratory, and facility activities; support data integrity initiatives for the site. | 2/15/2024 |
| 3243 | Mirati Therapeutics Devens, MA Specialist, Validation Engineer I, Cleaning Validation Knowledge of Engineering and Quality Assurance generally attained through studies resulting in a B.S., in engineering, a related discipline. Exp: 0-2 years |
Supports the design and maintenance of a robust cleaning validation lifecycle for process equipment and systems, that includes a bench-scale cleaning program, a cleaning monitoring program, and a cleaning verification changeover program for a fully automated, multi-product biologics manufacturing facility. Performs cleaning validation lifecycle activities, including work arising from change controls, capital projects, shutdown/changeover activities, cleaning validation bench-scale studies, and cleaning monitoring programs. Works collaboratively with peers within Validation, Manufacturing Systems, Information Technology, Manufacturing, Manufacturing Engineering and Quality Effectively manages workload to address priorities, meet schedules, maximize productivity, reduce costs, and increase efficiencies. Ensures alignment with site validation master plans and philosophies, BMS policies, and industry guidelines on validation and quality engineering. | 2/15/2024 |
| 3244 | Miromatrix Medical Woburn, MA Research Associate I, Cell Production and Tissue Engineering Bachelor’s Degree in cellular biology, developmental biology, biomedical engineering, or a related field. Exp: 1+ years |
The Research Associate I is responsible for helping to derive and expand the necessary cell types to develop and build autologous tissue constructs as a solution to end-stage renal disease and other disorders. This position is part of a multidisciplinary team led by experienced stem cell and developmental biologists and engineers. This individual is experienced in human primary cell and stem cell derivation, expansion, and differentiation. Technical expertise in multiple cell biology techniques including quantitative polymerase chain reaction, fluorescence microscopy, flow cytometry and other immune-based assays are critical to this position. | 2/15/2024 |
| 3245 | Miromatrix Medical Eden Prarie, MN Research Associate II/Senior Research Associate, Cell Development & Characterization Research Associate II: Master’s degree in biology, cellular and molecular biology, biomedical sciences, biomedical engineering, or biomanufacturing. Exp: 1+ years’ |
The Senior Research Associate/Associate II, Cell Development and Characterization, is responsible for performing cellular analysis of primary kidney and liver cells using flow cytometry, immunofluorescence, immunocytochemistry, and qPCR. This individual must be self-motivated with demonstrated ability to culture and characterize mammalian cells, creatively solve problems, should be excellent at troubleshooting, and able to work independently and in collaboration with a diverse team of multidisciplinary scientists and engineers diligently and carefully. This role, and team, will be tasked with characterization of kidney and liver cells for cellularization efforts in Bioengineered Organ Development, and with developing GMP level protocols and release tests in preparation of IND filing. | 2/15/2024 |
| 3246 | Moderna Therapeutics Norwood, MA Research Associate, Technical Development Operations BS in Biochemistry, Molecular Biology, or a related field. Exp: 1-2 years |
Moderna is seeking a molecular biologist to join Technical Development newly established Sequencing Center. In this laboratory-based position, the individual will routinely process sequencing samples, operate, and troubleshoot instruments including ABI 3730xl, Echo, Illumina MiSeq, NovaSeq, plate readers and liquid handlers. Experience with lab automation is a plus. The candidate must thrive in a fast pace high throughput environment, have a collaborative spirit, and be curious and willing to learn new techniques to push process development forward. | 2/16/2024 |
| 3247 | Moderna Therapeutics Norwood, MA Research Associate, Analytical Development A BS with a focus on microbial sciences. Exp: 1+ years |
We seek a motivated individual with experience in a microbiology laboratory setting to support microbial testing in Technical Development. Candidates should have experience with various microbial techniques such as aseptic sample handling, filtration and pipetting. In this laboratory-based role, the Research Associate will be responsible for supporting daily laboratory operations and following microbiology test protocols for analysis of in-process and final product bioburden and endotoxin release testing of development samples (DNA plasmid, protein, mRNA, and LNP sample types). In addition, the Candidate would contribute to method optimization, testing in support of rapid microbiological method qualifications and maintain the microbiology laboratory and equipment. | 2/16/2024 |
| 3248 | Moderna Therapeutics Norwood, MA Research Associate, Drug Product Development Masters or Bachelor’s Degree in on one of the following fields: Chemical Engineering, Biochemical or Biomedical Engineering, Pharmaceutical Sciences, Exp: 0 – 2 years |
We are seeking a highly skilled and motivated Research Associate in Drug Product Development respiratory team, to work in a team developing Moderna’s sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support product concept development including process development and scale-up work, container development and conditions of use studies. The incumbent will support the development of compositions, aseptic fill/finish unit operations through the development and use of scale-down models, process characterization studies etc. Applicants should have relevant pharmaceutical sciences related experience with various aspects of drug product development. The applicant should have exceptional ability to plan, execute and report, to communicate and collaborate, and requires strong attention to detail while working in a fast-paced, interdisciplinary environment. | 2/16/2024 |
| 3249 | Moderna Therapeutics Norwood, MA Engineer II, MST Biochemical engineer, Chemical engineer, Biochemistry or Biology background. MS. Exp: 1 to 3 years’ |
The Engineer II, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross-functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 3rd shift role, working a Wednesday through Saturday schedule from 10:00pm until 8:00am. | 2/16/2024 |
| 3250 | Moderna Therapeutics Norwood, MA Engineer I, MS&T Biochemical engineer, Chemical engineer, Biochemistry or Biology background. BS. Exp: 1 to 2 years |
The Engineer I, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 3rd shift role, working a Sunday through Wednesday schedule from 10:00pm until 8:00am. | 2/16/2024 |
| 3251 | Moderna Therapeutics Norwood, MA Engineer I, MS&T Biochemical engineer, Chemical engineer, Biochemistry or Biology background. BS. Exp: 1 to 2 years |
The Engineer I, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 3rd shift role, working a Wednesday through Saturday schedule from 10:00pm until 8:00am. | 2/16/2024 |
| 3252 | Moderna Therapeutics Norwood, MA Engineer II, MST - PCV Biochemical engineer, Chemical engineer, Biochemistry or Biology background. MS. Exp: 1 to 3 years’ |
The Specialist, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Personalized Cancer Vaccine (PCV). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 1st shift role and the individual will be working a Wednesday through Saturday schedule from 6:00am until 4:00pm. | 2/16/2024 |
| 3253 | Nanostring Bothell, WA Manufacturing Assembly Technician I 2-year degree in a Life Science related discipline (Chemistry, Molecular Biology, Biotechnology, etc.) Exp: 0+ years |
The Manufacturing Lab Technician is responsible for supporting the production of reagents used in various NanoString Analysis Systems, for example, nCounter® and GeoMx®. The role requires learning and performing both manual and automated production processes for the manufacturing of raw, intermediate, and final reagents needed for the multiplexed detection and the quantification of many different types of target molecules from biological samples. In this role, the Lab Tech will learn the skills to operate semi-automated and automated scientific equipment, perform Standard Operating Procedures (SOPs), navigate Document Control systems, Enterprise Resource Planning (ERP) systems, etc. | 2/16/2024 |
| 3254 | Nanosyn Mississauga, Ontario Canada, CA Chemist I (Trace Metals) B.Sc. in chemistry or related field. Exp: 1 -2 years’ |
Under the supervision of the Supervisor, Trace Metals and Manager, Trace Metals and GMP Testing, this position is responsible for the following: Perform routine chemical and physical analysis on the full range of analytical samples in accordance with in-house methods, customer’s method or compendial method primarily using Inductively Coupled Plasma Mass Spectrometry (ICP-MS)/ Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES)/ Atomic Absorption Spectroscopy (AAS) Perform and maintain Trace Metals instruments- performance verifications, troubleshoot when required Assists with method development, method validation testing and analytical method transfer testing using ICP-OES/ ICP-MS/ and AAS Prepare analytical reports, method validation protocols and reports for validations and verifications performed Maintain documentation, including lab notebooks, equipment logbooks and instrument raw data in accordance with applicable SOPs Inform and discuss with Manager any atypical / OOS result and deviations Perform pipette calibrations, washing of glassware, disposal of samples in accordance with in-house SOPs Assist Supervisor and Manager with other laboratory duties as required | 2/16/2024 |
| 3255 | Nanosyn Acton, MA Microbiologist I (Entry Level) Graduation in microbiology / equivalent. Exp: 1-2 year |
Element has an opportunity for a Microbiologist I whose primary responsibility is to support laboratory operations by conducting the relevant microbiological testing. | 2/16/2024 |
| 3256 | Nanosyn Midland, MI Chemist Bachelors. Exp: 0-2 years’ |
Element has a current opening for a Chemist to join our growing team in Midland, MI. The Chemist executes analytical methods and perform testing using a variety of technologies, under the supervision of more senior staff members and supervisor. | 2/16/2024 |
| 3257 | New England Biolabs Ipswich, MA Research Technician B.A or B.S. in Biology, Molecular Biology or related field. Exp: 1+ years |
The Sequencing Core at New England Biolabs Inc. (NEB) is seeking a Research Technician to support Next-Generation sequencing (NGS) and DNA analysis operations of the group. As a member of the Sequencing Core, this individual will interface with scientists across the Research, Product Development, and Production departments to deliver high-quality data. | 2/16/2024 |
| 3258 | NorthEast BioLab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: Entry Level |
NOTE: PLEASE SUBMIT BOTH RESUME AND COVER LETTER TO APPLY FOR THIS JOB. KINDLY DISCUSS YOUR MOTIVATION, RELEVANT EXPERIENCE, SALARY REQUIREMENTS, AND VISA STATUS IN YOUR SUBMISSION. Role Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices Follow appropriate safety and study requirements by reading, understanding, and following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) requirements, and Sponsor Study protocols Support business development and marketing activities, foster client relationships, and help onboard new sponsors | 2/16/2024 |
| 3259 | Nelson Laboratories Taylorsville, UT Lab Analyst - Routine Chemistry (Day Shift, Mon-Fri) Bachelors Degree is relevant Life Science preferred. Exp: No Experience |
Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. | 2/16/2024 |
| 3260 | Nephron Pharmaceuticals West Columbia, SC Quality Assurance Associate High School diploma with Bachelor of Arts or Science degree preferred. Exp: 1 year |
Manages the sampling, inspection, and release of production components, raw materials, as well as related corresponding documentation for use in manufacturing operations. Serves as primary reviewer for DHR documents and product release. Quality assurance process improvements. Coordinate incoming inspection equipment usage and maintenance. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. | 2/16/2024 |
| 3261 | Nephron Pharmaceuticals West Columbia, SC Microbiology Environmental Monitoring Technician - (Days & Nights Available) Associates of Science minimum; Bachelor’s degree with a science background preferred. Exp: 1+ years |
The Microbiology Environmental Monitoring (EM) Technician I is an entry level position that performs monitoring of air quality, environmental, and personnel throughout the facility. EM Technician I collects samples of water for injection (WFI) and performs enumeration. EM Technician I assists EM Leads, Supervisors, and Management with additional responsibilities as delegated. EM Technician I must uphold cGMP and Nephron’s core beliefs. | 2/16/2024 |
| 3262 | Nephron Pharmaceuticals West Columbia, SC Nitrile-QA Incoming Inspector Bachelor’s degree preferred. Exp: 1 year |
Receives, samples, inspects, and releases raw material chemicals within Nephron Nitrile’s electronic inventory system and process corresponding documentation necessary in manufacturing operations. Samples, inspects, and releases production components within Nephron Nitrile’s electronic inventory system. Ensures correct paperwork was obtained by warehouse personnel. Work with other departments to ensure receipts, sampling, and releases are within compliance and completed in a timely manner. Assists and performs additional work duties or responsibilities as evident or required. | 2/16/2024 |
| 3263 | Nephron Pharmaceuticals West Columbia, SC Microbiology Gowning Certification Coordinator Bachelor’s degree with a science background preferred. Exp: 1+ years |
The Microbiology Gowning Certification Coordinator is an expert on gown certification. Microbiology Gowning Certification Coordinator will lead all gown certification training and plating, as well as follow up with any re-training or re-certification necessary. Microbiology Gowning Certification Coordinator will maintain the certification schedule. When EM Trainer is unavailable, Microbiology Gowning Certification Coordinator will train EM Technician I and EM Technician II. Microbiology Gowning Certification Coordinator must uphold cGMP and Nephron’s core beliefs. | 2/16/2024 |
| 3264 | Neurocrine Biosciences San Diego, CA Associate Scientist, Analytical Chem Research Bachelor's degree in Chemistry, Biochemistry or similar discipline. Exp: 1+ years |
Assists medicinal chemistry efforts in purifying and analyzing small molecules by LC-MS and SFC. Supports a range of activities, including design, operation, and maintenance of all analytical instrumentation, including HPLCs, SFCs, mass spectrometers, liquid handlers, and solvent evaporators. | 2/16/2024 |
| 3265 | Nexcelom Bioscience San Diego, CA Research Associate I - Diagnostics Bachelor’s degree in a Life Sciences-related field. Exp: 1 years |
BioLegend (a division of Revvity, Inc.) is seeking a highly motivated Product Development Research Associate to join our Diagnostic Product Development Team. This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report. | 2/16/2024 |
| 3266 | Nexcelom Bioscience San Diego, CA Research Associate I - Antibody Development Bachelor of Science or equivalent degree with coursework in cell biology, immunology, and biochemistry. Exp: 1+ years |
This person would be responsible for developing monoclonal (or polyclonal) antibodies in BioLegend derived from immunized animals by performing antigen preparation, host immunization, bleed analysis, cell fusion, and small-scale antibody purification. Techniques involved in this job include antigen formulation, animal immunization and tissue harvesting, cell culture, cell fusion, and antibody analysis using ELISA, WB, and other techniques. | 2/16/2024 |
| 3267 | Lifecore Biomedical Chaska, MN Associate Manufacturing Engineer - Automation BS in Engineering or Automation Engineering Technology Degree. Exp: entry level |
This full-time position offers incredible benefits, your choice of a 2nd shift - 4 day work week or a weekend shift - 3 day work week, and a company culture focused on development and growth which include promotion opportunities. In this entry level engineering role you'll have the opportunity to utilize and enhance your skills in a highly regulated industry by supporting automated manufacturing processes by designing and implementing improvements and troubleshooting and resolving issues. | 2/5/2024 |
| 3268 | Lifecore Biomedical Chaska, MN QC Lab Coordinator I Bachelor’s Degree in life science or equivalent combination of education and experience. Exp: 1-3 years |
This full time position offers incredible benefits, your choice of a 4 ½ or 5 day work week, and a company culture focused on development and growth which include promotion opportunities. As the QC Lab Coordinator, you will support the Quality Control department in meeting their goals and accountabilities by trending department data and reporting key metrics. You will manage scheduling and coordinate with other departments to ensure timelines are maintained. You will also perform LIMS and ERP transactions, coordinate with external vendors, and assist with creating, updating, and reviewing supporting QC documentation. | 2/5/2024 |
| 3269 | Lonza Durham, NC Cell Culture Technician AA degree Exp: 1-3 years |
Lonza Durham has an exciting opportunity for a Cell Culture Technician to perform tissue culture, tissue isolations and media production with a high degree of aseptic and technical skill. The Cell Culture Technician facilitates departmental function including training lower-level technicians, laboratory maintenance and cleaning, assisting with planning and ordering, writing protocols, performing and reporting on experiments, upholding departmental standards, and reviewing batch records. The Cell Culture Technician is responsible for the manufacture and assembly of products used in clinical research including operation of production equipment, maintaining records, and laboratory environment to comply with Good Manufacturing Practices (GMP), ISO 9000 regulations, and Standard Operating Procedures. The Cell Culture Technician may assist with in process testing to assure batches meet specifications. The training schedule, following orientation, will be Monday – Friday, 8am – 5pm for up to 12 weeks. After training, the work schedule will be Tuesday - Saturday, 8am – 5pm. Occasional evening and weekend work required | 2/5/2024 |
| 3270 | Lonza Portsmouth, NH Manufacturing Project Associate 2 (Biologics Manufacturing) A.S. or B.S. degree preferred, with a focus in Biotechnology, Biology, Chemistry, or related STEM discipline. Exp: 1+ years |
The Manufacturing Project Associate Level II is an intermediate level position for an individual with technical manufacturing knowledge and preferably prior proven projects experience. As a level II, the individual is responsible for medium to large sized suite and process specific projects and projects that span across suites and/or the entire Manufacturing organization. The individual is responsible for owning and driving manufacturing improvement projects from concept to completion, with a particular focus on creating efficiencies that contribute to quality, cost, on-time delivery and right first time. The Project Associate supports by working cross-functionally and in collaboration with internal support departments, vendors, and Manufacturing suites to implement new systems, technology and/or procedures, update/create associated documentations and provide essential trainings. The individual will be expected to manage a number of projects at various stages of completion; managing priorities and ensuring on time and quality delivery of all assigned projects. In this level, individuals may become introduced to more customer and campaign focused responsibilities, including IPT/JPT and pre-campaign initiatives. | 2/5/2024 |
| 3271 | Lonza Portsmouth, NH Manufacturing Project Specialist (Biologics Manufacturing) A.S. or B.S. degree highly preferred, with a focus in Biotechnology, Biology, Chemistry, or related STEM discipline. Exp: 1+ years |
The Manufacturing Project Specialist works closely with Manufacturing Management to support the achievement of department goals, interdepartmental readiness and batch release requirements, and maintain due dates to support the on time release of batches. The Project Specialist supports by working cross-functionally and in collaboration with internal support departments, customers and Manufacturing suites to develop or update procedures or steps, identify and escalate risks, communicate changes and plan for execution. The Project Specialist is responsible for owning and driving manufacturing improvement projects from concept to completion, with a particular focus on creating efficiencies that contribute to quality, cost, on-time delivery and right first time performance. This role falls under Lonza's Hybrid Work Policy, which requires 3 days a week onsite. | 2/5/2024 |
| 3272 | Lonza Portsmouth, NH Biotechnologist Level 1 (A Shift Days) AS/BS preferred; Science related discipline. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Biotechnologist/Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks | 2/5/2024 |
| 3273 | Lonza Portsmouth, NH Biotechnologist Level 2 (Upstream) - A Shift Days AS/BS preferred in relevant STEM field. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH The Biotechnologist Level 2 is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level II associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. | 2/5/2024 |
| 3274 | Lonza Portsmouth, NH Biotechnologist Level 1 (B-Nights) - Biotech Manufacturing AS/BS preferred; Science related discipline. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7pm-7am, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for night shift and for weekends worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Biotechnologist/Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. | 2/5/2024 |
| 3275 | Lonza Portsmouth, NH Biotechnologist Level 1 - Cell Therapy A.S., B.S., or vocational certificate in relevant STEM field is a plus. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Cell & Gene Therapy Biotechnologist/Manufacturing Associate will help to provide a safe, controlled work environment in all areas of expertise. Be aware of the site safety objectives and make sure they are communicated and understood. Biotechnologist/Manufacturing Associates will be proficient in an assigned area (i.e. Cell Growth, Drug Product Filling, etc.) and work in a team environment during manufacturing operations (i.e. harvest, fill/finish, visual inspection, etc.). | 2/5/2024 |
| 3276 | Loop Genomics San Diego, CA Research Associate, Surface Chemistry Bachelor’s degree in chemistry, materials science, biochemistry, bioengineering, physics, or similar fields. Exp: 0-2 years |
We are seeking a Research Associate, who has a curious mind and a great desire to learn new techniques in new areas of study to join our interdisciplinary research team. You will be learning experiment design pertaining to surface coating characterization assays, explore optimal surface coating process and support custom surface production needs. The preferred candidate will have scientific research lab experience, demonstrated by any combination of prior curricular, extracurricular undergraduate research lab work, scientific paper, poster, or presentations. | 2/5/2024 |
| 3277 | LSI Solutions Victor, NY Manufacturing Engineer - 8:00AM to 5:00PM Level I: BS Engineering or Engineering Technology; or Level II: MS. Exp: Level I: 0-2 years; Level II: 1 to 5 years |
The Manufacturing Engineer is responsible for developing and improving manufacturing processes. They design and refine production equipment and processes to improve capability, enhance productivity, reduce waste, reduce risk, and elevate overall product quality. Manufacturing Engineers introduce new technologies, perform root cause analysis, implement corrective actions, and leverage problem solving skills and equipment expertise to support ongoing production. | 2/5/2024 |
| 3278 | Lumen Bioscience Seattle, WA Lab Technician, Physiology BA/BS degree in molecular biology, microbiology, biochemistry, chemistry, biotechnology, biochemical engineering, or related field of study Exp: 1-3 years |
Lumen is seeking a highly motivated, innovative Lab Technician to join our team. The Laboratory Technician will support scientists in the Physiology research and development group. The work will involve several projects aimed at culturing Lumen’s spirulina-based platform organism. The individual will be focused on operating bioreactors under various run conditions and analyzing samples. The candidate is also expected to independently perform and learn new laboratory techniques, use specialized laboratory instruments, perform delicate manual procedures, follow and apply standard laboratory protocols and provide reliable, independent, and versatile support to biotechnology research. The position requires strong organizational skills and meticulous laboratory record keeping. Effective communication skills are crucial in coordinating with Lumen’s research and production scientists, in providing status updates, and in raising quality or troubleshooting issues as they may arise. | 2/5/2024 |
| 3279 | Lumen Bioscience Seattle, WA Lab Technician, Clinical B.S. in immunology, biochemistry, cell biology, microbiology, or related field of study. Exp: one year |
Lumen Bioscience Clinical Program Management is seeking a laboratory technician with clinical research laboratory experience. Working with scientists, the technician will support assay development efforts across multiple active clinical projects. The position also involves coordinating assay development internally with Lumen’s research, manufacturing, and quality teams. The technician will support equipment and supply requisition and inventory. In addition, the technician will maintain the clinical specimen archive. The position requires strong communication skills and an empathic understanding of where others are experiencing issues. Efficient problem-solving are crucial to keep pace with our growing company. Personal initiative and organizational skills will drive your career growth. | 2/5/2024 |
| 3280 | Luminex Madison, WI Design Assurance Engineer Bachelor's Degree Bachelor degree required, in a life science/engineering discipline required. Exp: 1+ Years |
The Design Assurance Engineer acts as the quality representative on design core teams for electromechanical instruments, reagents and assays for the life science and in-vitro diagnostics market. Design Assurance Engineer is responsible for guiding the development teams through the Design Control process ensuring compliance with FDA, ISO, QSR, quality, safety and environmental regulations and internal procedures. The Design Assurance Engineer may also provide support for quality initiatives, post market design changes/improvements and quality surveillance activities. | 2/5/2024 |
| 3281 | Luminex Northbrook, IL Manufacturing Associate I, Microarray Associate's Degree in Chemistry, Life Sciences, Biotechnology, or Medical Technology related fields required. Exp: 1+ Years |
Delivering manufacturing requirements against production schedule within a focused manufacturing operation and/or product segment. Work schedule may include alternate shifts. Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System. | 2/5/2024 |
| 3282 | Luminex Cypress, CA Cell Culture Technician II Requires Bachelor’s Degree in Biology or related field or equivalent experience. Exp: 1+ Years |
Responsible for manufacturing and assembly of clinical and commercial products. Operates production equipment. Weighs, measures and checks raw materials to assure batches manufactured contain proper ingredients and quantities. Performs Cell Culture activities using aseptic technique. Maintains records and laboratory environment to comply with regulatory requirements, Good Manufacturing Practices and Standard Operating Procedures. Assist with in-process testing to assure batches meet specifications. Assignments are moderately complex in nature where judgment is required in resolving problems and making routine recommendations. Supports all applicable regulations including but not limited to FDA, ISO, and CMD/CAS requirements. | 2/5/2024 |
| 3283 | Luminex Stillwater, MN Process Scientist I Bachelor's or Master's degree in Chemistry, Biology, Medical Technology or related science field. Exp: 1+ years |
This position is responsible for material processing, reagent formulation, technical manufacturing, in-process and final quality control of reagents, components and in-vitro diagnostic products. | 2/5/2024 |
| 3284 | Luminex Stillwater, MN Engineering Technician BS in Engineering Exp: 1-2 years |
As an Equipment Technician, you will be an administrator and expert of the equipment used in the manufacture of in vitro diagnostic products. In addition, you will drive operational improvement activities that involve equipment procurement, validation, or the transfer of information from equipment. This is a fast-paced, deadline-driven department that provides centralized support to the organization. Be a Subject Matter Experts (SME) for equipment and equipment validations to implement changes to business systems and processes, interacting and working collaboratively with teams across Diasorin. | 2/5/2024 |
| 3285 | Horizon Therapeutics Thousand Oaks, CA Engineer Master’s degree in Engineering Exp: 0 - 2 years |
Let’s do this! Let’s change the world! In this dynamic role you will serve as the system owner for process equipment in a state of the art bulk biopharmaceutical manufacturing facility. | 2/7/2024 |
| 3286 | Horizon Therapeutics Holly Springs, NC Engineer - Plant Utilities Master’s Degree in Chemical or Mechanical Engineering Exp: 0 - 2 years |
Let’s do this! Let’s change the world! The Engineer System Owner will be joining the Facilities & Engineering (F&E) group to partner closely with the corporate engineering team to design, build, commission, and qualify new equipment and systems needed for drug substance production, as well as developing subject matter expertise to support operations upon start up. | 2/7/2024 |
| 3287 | HRA Pharma Covington, OH Microbiologist I - Nights A four-year college degree in Microbiology or Biological Science. Exp: One years |
Perrigo Nutritionals, located in Covington, OH is looking to add a Night shift Microbiologist to their team. The hours for this position are, 6pm - 6am working a rotating 2/2/3 schedule Scope of the Role The successful candidate will be able to work in a safe and efficient manner in accordance with current GLP’s, SOP’s, analytical methods, and work instructions. Excellent communication skills, attention to detail, and the ability to work both independently and as part of a team are desired. A thorough understanding of aseptic technique is essential. Microbiological testing is performed on raw materials, in-process samples, finished products, water samples, and environmental swab samples. | 2/7/2024 |
| 3288 | HRA Pharma Georgia, VT Chemistry Analyst I - 2nd Four-year college degree in chemistry or related science. Exp: 1-2 years |
The incumbent performs a variety of standard analyses on raw material, in-process, and finished product samples using chemical analysis techniques, according to compendia (i.e. USP, FCC, or AOAC) or Perrigo methodologies. Performs routine analyses of raw material and finished product samples as assigned, demonstrates proficiency in 5 – 10 separate Analytical Methods (AM’s). Analytical instrumentation used in this group is primarily NMR Fat Analyzer, Nitrogen Analyzer, NIR Spectroscopy, and HPLC (High Pressure Liquid Chromatography). | 2/7/2024 |
| 3289 | ICU Medical Austin, TX Chemistry Analyst I - Night Shift - (24300022) Bachelor’s Degree is required: Chemistry, Chemical Engineering, or Chemical Science. Exp: 0-2 year |
The Chemistry Analyst I will work under direct supervision or be partnered with an experienced analyst to perform wet chemistry analyses, preparation of reagents, standardization of solutions, and instrumentation testing and documentation in a cGMP environment. May be cross-trained to work in other laboratory areas as dictated by the needs of the department. | 2/7/2024 |
| 3290 | Integrated DNA Technologies Coralville, IA Technician II Associate’s (2 year) degree. Bachelor’s (4 year) degree preferred. Science related field preferred. Exp: 1+ years |
This position is part of the Production department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Sunday – Thursday 3:00PM – Midnight | 2/7/2024 |
| 3291 | Integrated DNA Technologies Coralville, IA Job Posting Title Technician II (Synthesis -Long Oligo) Associate or bachelor’s degree in a Science related field preferred. Exp: 12 months |
This position is part Shipping, Receiving and Distribution department of the located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Monday-Thursday 9:00pm-7:30am | 2/7/2024 |
| 3292 | Integrated DNA Technologies Coralville, IA Technician II (Synthesis - MNP) Associate or bachelor’s degree in a Science related field preferred. Exp: 12 months |
This position is part Shipping, Receiving and Distribution department of the located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Wednesday -Friday 7PM-7AM. | 2/7/2024 |
| 3293 | Integrated DNA Technologies Coralville, IA Technician II, Stock Product Associate’s (2 year) degree or comparable combination of education and experience required. Bachelor’s (4 year) degree preferred. Science related fi Exp: 1+ years |
This position is part of the Production department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Sunday – Thursday 3:00PM – Midnight | 2/7/2024 |
| 3294 | Integrated DNA Technologies Coralville, IA Technician II (Formulation - GMP) - Overnight Associate’s (2 year) degree or comparable combination of education and experience required. Bachelor’s (4 year) degree preferred. Science related fi Exp: 1+ years |
This position is part of the Production department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Weekday Overnight; Monday – Thursday 8:30pm-7:00am | 2/7/2024 |
| 3295 | Illumina San Diego, CA Scientist 1: Assay Product Development BS/MS in Biochemistry, Molecular Biology, Chemistry, Biology, Bioengineering, or related disciplines. Exp: 1-2 years |
We are looking for a contract Scientist 1 to join the assay development team within Illumina Product Development. This person will be contributing to new technologies and workflows for Illumina customers as part of a collaborative team. This is a hands-on position where you will primarily be responsible for the design, execution, and analysis of experiments to support assay development and optimization. | 2/7/2024 |
| 3296 | Lyophilization Services of New England Bedford, NH QA Associate I - Operations Bachelor’s Degree in a relevant scientific discipline preferred. Exp: 0-2 years |
The Quality Associate I - Operations is responsible to provide QA support real-time for GMP Manufacturing of drug product. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products. | 2/8/2024 |
| 3297 | Lyophilization Services of New England Madison, WI QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study. Exp: 0-3 years |
The QC Chemist I will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management | 2/8/2024 |
| 3298 | Lyophilization Services of New England Bedford, NH QA Associate I - Operations Bachelor’s Degree in a relevant scientific discipline preferred. Exp: 0-2 years |
The Quality Associate I - Operations is responsible to provide QA support real-time for GMP Manufacturing of drug product. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products. | 2/8/2024 |
| 3299 | Maverick Therapeutics Social Circle, GA Manufacturing Technician II AA or higher. Exp: 1+ years |
As a Manufacturing Tech II, you will execute all processes in production while strictly following cGMP, environmental health and safety guidelines and any other related regulations which could apply. In addition to making routine revisions to documents, you may rewrite complex procedures or initiate new procedures as applicable. You will have enough applied technical knowledge to perform complex trouble shooting tasks and may even assist during the transfer of new technologies into manufacturing. You will have technical and administrative competence to organize and lead production activities, including demonstrating leadership in cGMP compliance, and environmental health and safety skills. You will report to Manufacturing Supervisor. | 2/9/2024 |
| 3300 | Maverick Therapeutics Thousand Oaks, CA Manufacturing Associate - Day Bachelor's degree preferred. Exp: 0-2 years |
Under the general direction of the Manufacturing Lead and overall direction of the Supervisor, the Manufacturing Associate executes all processes in the production area while strictly adhering to CGMP, environmental health and safety guidelines and any other related regulations. | 2/9/2024 |
| 3301 | Maverick Therapeutics Round Lake Beach, IL Manufacturing Technician II AA or higher. Exp: 1+ years |
As a Manufacturing Technician II, you will implement all processes in production while strictly following cGMP, environmental health and safety guidelines and any applicable related regulations. You will have technical and administrative competence to organize and lead production activities. You will participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include assisting with the movement of Flexbumin between the different stages of inspection to packaging within the value stream. You may act as line lead, and will ensure the line operates smoothly and keeps up with daily goals. You will also document your process activities on routers or in the electronic batch management system (EBM). You will report to the Supervisor, Manufacturing. | 2/9/2024 |
| 3302 | Maverick Therapeutics Thousand Oaks, CA Manufacturing Associate - Night Shift Bachelor's degree preferred. Exp: 0-2 years |
Under the general direction of the Manufacturing Lead and overall direction of the Supervisor, the Manufacturing Associate executes all processes in the production area while strictly adhering to CGMP, environmental health and safety guidelines and any other related regulations. This position is a night shift role. | 2/9/2024 |
| 3303 | Medtronic Cherry Hill, MA Microbiologist II Bachelors degree required. Exp: one year |
Responsibilities may include the following and other duties may be assigned. Interacts with Purchasing and Contract Sterilization/Test Facilities to ensure that the Sterilization requirements and product testing procedures are clear, complete and understood. Works with the internal personnel as well as with the Contract Sterilization and Test facilities to establish specifications and coordinates the new product sterilization validations as well as the quarterly validations. Work with different Subject Matter Expert to evaluate changes impacting the product families, controlled rooms and critical systems. Coordinates yearly and quarterly product re-verifications (Irradiation & Ethylene Oxide)Coordinate lethality testing for EO product, or process qualifications Product Release (EO & Gamma) Develop and Coordinate Steam Sterilization Studies Develop and Coordinate Reusable Device Validation (Cleaning Studies) Develop and Coordinate Profiling Protocols | 2/9/2024 |
| 3304 | Medtronic Northridge, CA Biomedical Engineer II Masters of Science in Biomedical Engineering, Chemical Engineering, or related disciplines. Exp: 0+ years |
As a member of the Medtronic Diabetes – Continuous Glucose Monitoring Sensor R&D team this Product Development Engineer II will support the development of next generation CGM products. This position will play a key role in the early stage development of various new/improved chemistry layers/coatings of glucose sensors by designing and executing design optimization and characterization studies in preclinical & clinical studies. The role includes process development for feasibility clinical manufacturing. To this end, you will be responsible for driving the product build documentation, coordinating the fabrication & builds of prototype sensors for benchtop, preclinical and clinical evaluations, execute data trending & statistical process analysis. Upon successful proof-of-concept through feasibility studies, this role will subsequently support tech transfer to process & manufacturing teams. You will manage deliverables for multiple projects and maintain an effective system for tracking progress. You will be interfacing with Managers, Engineers &Technicians in R&D and New Product Introduction (NPI) Operations teams as well as Quality and Clinical groups to accomplish day to day activities. The candidate must have strong organizational skills, attention to details, an analytical mindset and ability to communicate effectively with multiple stakeholders. | 2/9/2024 |
| 3305 | Medtronic Bedford, MA Quality Engineer II Advanced degree in related engineering discipline required (Biomedical, mechanical, manufacturing, etc.). Exp: 0 years |
In this exciting role as a Quality Engineer II in the Bedford/Billerica facilities, you will have responsibility for supporting the quality and daily manufacturing of high-quality and complex catheters to support the Cardiac Ablation Solutions Business. In this role you will be part of a team that grows the operations capacity over 8X to support our customer needs in this newly acquired product portfolio. You will lead improvements in manufacturing quality, capacity, and stability through solving problems, developing solutions, and executing strategies. | 2/9/2024 |
| 3306 | Medtronic Billerica, MA Manufacturing Engineer II Advanced degree. Exp: 0 years |
Responsibilities may include the following and other duties may be assigned. Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapts machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques. Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. | 2/9/2024 |
| 3307 | Genentech Hillsboro, OR MANUFACTURING ASSET ENGINEER I/II, HTO B.S or higher in Mechanical Engineering, Electrical, Chemical, Biochemical, or related discipline. Exp: 0-2 years’ |
The Asset Engineer I/II is responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as the equipment owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Asset Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 1/25/2024 |
| 3308 | Genentech Hillsboro, OR MANUFACTURING TECHNICIAN (CONTRACTOR) Graduate of a two-year Associates Degree program in Electrical/Mechanical Technology (or equivalent) is a plus. Exp: 1 to 2 years (within the last 7 years) |
Under the direction of the Process Unit Lead, perform a wide variety of tasks and operations that are required to formulate, fill, inspect and package sterile pharmaceutical products in a state-of-the-art, automated production and packaging facility. Troubleshoot, maintain, assemble, install, and repair all electronic, mechanical, and instrumentation devices on production equipment as required. Assist on major equipment overhauls, repairs, and installations as necessary. All operations carried out in compliance with cGMPs, Standard Operating Procedures (SOPs), product recipes, and Genentech standards. Duration: 6-month contract with possible extensions up to 3 years Day Shift, 6:00 am – 6:30 pm, Sunday -Tuesday plus every other Wednesday Day Shift, 6:00 am – 6:30 pm, Thursday -Saturday plus every other Wednesday Day Shift, 5:30 am - 4:00 pm, Monday - Thursday Swing Shift, 12:00 pm -10:30 pm Monday - Thursday Night Shift, 6:00 pm -6:30 am, Sunday-Tuesday plus every other Saturday Night Shift, 6:00 pm – 6:30 am, Wednesday – Friday plus every other Saturday | 1/25/2024 |
| 3309 | Genentech Hillsboro, OR MANUFACTURING ASSET ENGINEER I, HTO (TWO YEAR TERM) B.S or higher in Mechanical Engineering, Electrical, Chemical, Biochemical, or related discipline. Exp: 1-2 years’ |
The Asset Engineer is responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as the equipment owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Asset Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 1/25/2024 |
| 3310 | Genentech Vacaville, CA MANUFACTURING TECHNICIAN-BIOPROCESS (CONTRACTOR) Desirable but not required: AS/BS/BA in Biological Sciences, Physical Sciences. Exp: 1+ years |
As a Manufacturing Technician, you will be responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in a current Good Manufacturing Practices (cGMP) environment. You will maintain areas in a high state of inspection preparedness and will utilize business systems for inventory and process management. You will maintain records to comply with regulatory requirements utilizing cGMP and Standard Operating Procedures (SOPs) and will participate in the routine production of mammalian cell culture products within the Vacaville Manufacturing Facility, operating in at least one of the following production areas: Upstream Manufacturing (UM): Primary focus is the cleaning, sterilization and operation of fixed vessel systems for media preparation, fermentation, and harvest operations; perform seed train operations; perform dispensing of components; handle and aliquot hazardous materials. Downstream Manufacturing (DM): Responsibilities include the operation and cleaning of fixed tank systems, the operation and cleaning of filtration systems, large-scale buffer preparation, and the operation of column chromatography systems; perform dispensing of components; handle and aliquot hazardous materials | 1/25/2024 |
| 3311 | Genentech Oceanside, CA BIOPROCESS MANUFACTURING TECHNICIAN (CONTRACT) Preferred - Degree in Life Sciences/Engineering, Associate’s or Biotech certificate from approved program. Exp: 1+ years |
At Genentech, we are dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. As a Bioprocess Manufacturing Technician, you will be responsible for producing medicine in a highly automated and controlled environment. Each product has a specific recipe; you will follow this recipe, along with the standard operating procedures, to operate the production equipment across various areas, including raw material dispensing/aliquoting, cell culture and purification. You will maintain records and follow all the steps necessary to comply with regulatory requirements within a current Good Manufacturing Practices (cGMP) environment. This is a contract role with the possibility of conversion to a permanent employee position. | 1/25/2024 |
| 3312 | Genentech Oceanside, CA ENGINEER I Bachelor's or Master's degree in Engineering or Life Sciences. Exp: 0-4 years |
Responsible for supporting operations in the Oceanside Pilot Plant and Process Engineering Purification/Analytical Lab. Deliverables include but are not limited to: HPLC-based analytics, rapid bioburden/endotoxin, lab scale and pilot scale chromatography, UFDF operations, buffer prep, column packing, equipment maintenance and preparation of technical reports. May commission new equipment, troubleshoot equipment and systems, develop new equipment requirements and operating parameters, and provide factory and site acceptance testing. Provide scientific and technical support to GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. Support process validation through large and small-scale studies, protocol and report preparation, validation sampling, and sample shipments. | 1/25/2024 |
| 3313 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Chemist I Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology). Exp: 1-3 years |
The Quality Control Chemist is responsible for supporting quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 1/25/2024 |
| 3314 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Lab Technician Bachelor’s degree in a related field (Biochemistry, Biotechnology, etc.). Exp: 0-2 years’ |
The QC Lab Technician supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include but are not limited to providing general laboratory support for sampling of raw material, incoming stability and finished product sample processing, basic physical testing, and inventory administration. | 1/25/2024 |
| 3315 | Grand River Aseptic Manufacturing Grand Rapids, MI Aseptic Manufacturing Associate (2nd and 3rd shifts) Bachelor’s degree, or equivalent experience. Exp: 0-1 year |
The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. | 1/25/2024 |
| 3316 | GreenLight Biosciences Rochester, NY Bioprocess Technician 4-year degree in Chemistry, Biochemistry, Biotechnology, Chemical Engineering. Exp: 1+ years |
GreenLight Biosciences is seeking a highly motivated Bioprocess Technician with education/experience in biotechnology, microbiology and biochemistry process operations at development scale. The successful candidate will become a member of the Rochester, NY pilot plant team and support their overall mission of delivering high performance RNA production processes and products to the market. Exact level dependent on qualifications including relevant experience. | 1/25/2024 |
| 3317 | Grifols Clayton, NC Utilities Project Engineer Bachelor's Degree in Engineering or related field. Exp: Engineer I: 0 years |
The Utilities Project Engineer will be responsible for the oversight of utilities projects for an industry leading biological therapeutic product manufacturer, Grifols as a member of the Facilities NA Project Engineering Team. The position will be stationed in Clayton, NC and will oversee Grifols projects on the east coast of the United States primarily, with the potential to oversee projects at other North American sites. Projects will include installation of clean and dirty utilities such as refrigeration systems, chillers, cooling towers, boilers, water purification systems, steam systems, waste systems, pumped distribution systems, and others, with some civil/structural oversight. Candidate should have a good understanding of the theory behind these types of systems as some system design and design reviews will be required. Candidate, through experience, should have knowledge of industry standards and best practices for utilities systems. Candidate must be willing to adjust working hours to meet the needs of the project(s), including some weekend work when required to match the schedule of project crafts. Some travel will be required - up to 25%. The position has the potential to progress into an engineering role / management role of increasing responsibility. | 1/25/2024 |
| 3318 | Grifols Vista, CA Manufacturing Technician Associates Degree or Bachelor’s degree preferred. Exp: 1-2 years’ |
Monday – Friday 6:30AM – 3:00PM The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 1/25/2024 |
| 3319 | Grifols Vista, CA Manufacturing Technician Associates Degree or Bachelor’s degree preferred. Exp: 1-2 years’ |
Monday – Friday 6:30AM – 3:00PM The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 1/25/2024 |
| 3320 | Grifols Los Angeles, CA QC Chemist Bachelor’s degree in Chemistry, Biochemistry, Biology or closely related scientific discipline is required. Exp: 1+ years |
The QC Chemist is responsible for performing routine and non-routine chemical and biochemical assays on protein-based therapeutics and raw materials. | 1/25/2024 |
| 3321 | Grifols Clayton, NC Quality Control Assistant/Associate Materials Eval. Coord. Associates degree with an emphasis in sciences or mathematics. Exp: one year |
Location: Clayton NC Shift: M-F 8am - 4:30pm The Quality Control Assistant/Associate Materials Evaluation Coordinator evaluates critical quality attributes (visual, dimensional, functional), coordinates required chemical and/or biological testing, and executes approved usage decisions on all quality managed material used at the facility. These evaluations are performed on a wide variety of materials including, but not limited to, chemicals, labeling components, primary drug container components, process hoses, sterilizing filters, and other critical raw materials. This is done by verifying compliance to specifications and testing requirements and ensuring required documentation is complete and accurate thus minimizing the possibility that the safety and efficacy of final products manufactured and tested using these quality managed materials is compromised or adulterated. The Coordinators perform the last detailed review of these materials prior to release for use thus sound judgment is essential. The QC Assistant/Associate Materials Evaluation Coordinator inspects product final container reserve samples according to approved standard operating procedures. The QC Assistant/Associate Materials Evaluation Coordinator may perform in the warehouse as a Quality representative for sampling, auditing, and making Quality decisions. In this area, the QC Assistant/Associate Materials Evaluation Coordinator audits raw material batches using designated ANSI sampling plans. Decisions made by QC Coordinators have major compliance and monetary implications for Grifols | 1/25/2024 |
| 3322 | GRO Biosciences Cambridge, MA RA/Senior RA, Application Sciences BS degree. Exp: 1 year |
We’re seeking an RA or a Senior RA with synthetic chemistry, protein biochemistry, and/or glycobiology experience who’s interested in learning new things, “wearing many hats”, and having a large impact on the growth of an early-stage company. Major responsibilities include experimental design, experiment execution, data analysis, and collaborating across a matrixed research team. Ideal candidates are collegiate, transparent, data-driven, motivated by novel challenges, and will think critically yet creatively about the company’s strategies for therapeutic development. | 1/25/2024 |
| 3323 | GlaxoSmithKline Marietta, PA Process Equipment Engineer BS Degree in engineering. Exp: 1 or more years |
Are you looking for an engineering role that allows you to leverage your technical knowledge in a state-of-the-art manufacturing environment? If so, this Process Equipment Engineer role could be an ideal opportunity to explore. The Process Equipment Engineer supports primary (bulk) vaccine adjuvant manufacturing in a 24/7 production facility as part of an Engineering and Maintenance Team. The team is responsible for maintaining equipment in a state of readiness through routine preventive maintenance and upgrades to extend its useful life. The Process Equipment Engineer will also lead continuous improvement projects to achieve Safety, Quality and Commercial objectives. As system experts, Engineers are relied upon to lead technical investigation impacting manufacturing processes | 1/25/2024 |
| 3324 | GlaxoSmithKline King of Prussia, PA Automation Engineer BS/BA in engineering, life sciences, biology or equivalent technical discipline. Exp: 3+ months |
As an Automation Engineer, you will provide engineering and technical support for process controls and manufacturing execution systems in the Biopharmaceutical Operations facility. Evaluate and develop technology, plan and implement modifications, troubleshoot and support process controls and manufacturing execution systems | 1/25/2024 |
| 3325 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 2:30pm - 1:00am) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 3326 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 7am - 5:30pm) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 3327 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Sun - Wed 7am - 5:30pm) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 3328 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Sun - Wed 2:30pm - 1:00am) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 3329 | Gyroscope Therapeutics Morris Plains, NJ Cell Processing Specialist I (Tuesday-Saturday am shift) Associate’s degree or Bachelor’s degree in relevant Engineering or Scientific discipline. Exp: 0 - 1+ years |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. Cell Processing Specialist I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 1/26/2024 |
| 3330 | Gyroscope Therapeutics Durham, NC BioProcess Engineer I - Upstream (2-2-3 rotation day shift) Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field. Exp: Entry level |
The BioProcess Engineer I is responsible for assisting with organizing, running, and sustaining the manufacturing operations process at the plant/site. | 1/26/2024 |
| 3331 | Gyroscope Therapeutics Morris Plains, NJ Cell Processing Specialist I Sun-Thurs. PM shift) Associate’s degree or Bachelor’s degree in relevant Engineering or Scientific discipline. Exp: 1 - 1+ years |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. Cell Processing Specialist I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 1/26/2024 |
| 3332 | HelixBind Boxborough, MA Research Associate BS in a Physical or Life Sciences/Engineering discipline. Exp: 1+ years |
We are seeking a talented and motivated individual to join our R&D Team as a Research Associate. The position offers the exciting opportunity to grow along with the Company as it takes its initial product through to FDA clearance and market launch while it, in parallel, grows its pipeline of impactful syndromic diagnostic assays. This is a great time to join the team, with plenty of opportunities to grow and lead new projects. | 1/26/2024 |
| 3333 | Helmer Scientific Noblesville, IN Electromechanical Engineer I BS degree in Engineering or Engineering Technology. Exp: 0-5 years |
This role supports Helmer Scientific, part of Trane Technologies Life Sciences Portfolio. Helmer Scientific designs, integrates, manufactures, markets, and distributes specialized medical and laboratory equipment to clinical and life science customers in over 125 countries, as well as provide after-market service and support. Provides electromechanical engineering support to Engineering department through the development, documentation and production support for Helmer product development. Develop specs for mechanical and electrical engineering requirements based on directions given by Manager. Have fundamental knowledge from educational background, while tasks are managed or directed by others | 1/26/2024 |
| 3334 | Heska Mississauga, On Temporary-Laboratory Generalist 1 - (Overnight) Associates/Bachelor’s Degree in Science related field or Veterinary Technician. Exp: 1 year |
Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. Shift: Monday - Friday 11pm - 7:30am Saturday on rotation | 1/26/2024 |
| 3335 | Heska West Palm, FL Stat Lab - Lab Generalist I Associates/Bachelor’s Degree in Science related field or Veterinary Technician. Exp: 1 year |
HOURS: The hours for this position are Monday - Friday from about 12:30pm - 6:30pm. PURPOSE OF JOB: Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. | 1/26/2024 |
| 3336 | Heska Chantilly, VA Lab Generalist I (overnight) Associates/Bachelor’s Degree in Science related field or Veterinary Technician Exp: 1 year |
Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. Shift: Monday - Friday 11:30pm - 8:00am Alternating Saturdays 10:00pm - 7:00am Includes night shift differential. ESSENTIAL DUTIES AND RESPONSIBILITIES: | 1/26/2024 |
| 3337 | Heska Irving, TX Lab Generalist I (Overnight) Associates/Bachelor’s Degree in Science related field or Veterinary Technician. Exp: 1 year |
Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. | 1/26/2024 |
| 3338 | Heska Mississauga, O Microbiology Technician I(Day Shift)Temporary 4 year degree in Science-related field preferred. Exp: 6 months |
The Microbiology Laboratory Technician I performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. Shift: Monday - Friday 9:00am - 5:30pm. Weekends would be on rotation. | 1/26/2024 |
| 3339 | Heska Oak Brook, IL Parasitology Technician 2, 3 or 4 year degree in Science-related field. Exp: 6 months |
The Parasitology Laboratory Technician performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. | 1/26/2024 |
| 3340 | Heska Atlanta, GA Parasitology Technician - Day Shift 2, 3 or 4 year degree in Science-related field. Exp: 6 months |
The Parasitology Laboratory Technician performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. SHIFT: Monday-Saturday 8am-430pm | 1/26/2024 |
| 3341 | Hikma Cherry Hill, NJ Chemical Process Operator I - 3rd Shift Associates Degree in Science or equivalent Exp: 1-year |
Using company procedures and guidelines, the Chemical Process Operator I is responsible for a limited spectrum of duties within the department. This may include weighing, mixing, equipment cleaning, tank cleaning, tank movement and PM activities, etc. This job has no supervisory responsibilities; however, the ability to assume higher level responsibilities and/or have demonstrated leadership abilities is preferred. | 1/26/2024 |
| 3342 | Hillrom Marion, NC Quality Lab Associate I - Bioburden (3rd Shift: M-Thu) B.S. degree in Microbiology, Biology, or related science. Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and components following approved Standard Operating Procedures in an accurate and timely manner. | 1/26/2024 |
| 3343 | Hillrom Plymouth, MN Engineer I - R&D Disposables (Hybrid) BS in Mechanical, Plastics, Biomedical Engineering or a related field, MS preferred. Exp: 0 - 1 year |
Document engineering concepts. Create, modify, and maintain design documentation per company procedures. Assist in the design and building of basic tooling, test fixtures and assembly equipment. Build prototypes and models and may operate machine tools. Understand customer needs through literature review, customer interviews, direct observation, competitive analysis, prototype evaluation, and clinical/simulated use studies. Write technical reports based on design verification analysis/testing for design changes and product design activities. Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis, and data analysis. Identify, investigate, and solve engineering problems. | 1/26/2024 |
| 3344 | Hillrom Marion, NC Quality Associate l (2nd shift:3pm-11pm) Bachelor's degree strongly preferred. Degree in engineering or life science preferred. Exp: 1+ years |
Responsible for working with the manufacturing departments to address defects with the finished products. | 1/26/2024 |
| 3345 | Hillrom Marion, NC Quality Lab Associate I- Bioburden (5th Shift- 6AM to 6PM) B.S. degree in Microbiology, Biology, or related science. Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and components following approved Standard Operating Procedures in an accurate and timely manner. | 1/26/2024 |
| 3346 | Hillrom Saint Paul, MN Manufacturing Engineer I B.S. degree in Engineering or Science (Biomedical Engineer, Chemical Engineer, Mechanical Engineer, Electromechanical). Exp: 1+ years |
As a member of St. Paul's Engineering team, the Manufacturing Engineer supports daily initiatives from manufacturing teams to equipment to integrate new products within production goals (i.e., quality, delivery, cost, productivity, and safety). In this role you will support engineering improvement projects, participate in R&D activities, support key development and continuous engineering projects, drive KPI implementation and follow up. | 1/26/2024 |
| 3347 | Companion Medical Danvers, MA Microbiologist II Bachelors degree required. Exp: 1-2 years |
Responsibilities may include the following and other duties may be assigned. Interacts with Purchasing and Contract Sterilization/Test Facilities to ensure that the Sterilization requirements and product testing procedures are clear, complete and understood. Works with the internal personnel as well as with the Contract Sterilization and Test facilities to establish specifications and coordinates the new product sterilization validations as well as the quarterly validations. Work with different Subject Matter Expert to evaluate changes impacting the product families, controlled rooms and critical systems. Coordinates yearly and quarterly product re-verifications (Irradiation & Ethylene Oxide)Coordinate lethality testing for EO product, or process qualifications Product Release (EO & Gamma) Develop and Coordinate Steam Sterilization Studies Develop and Coordinate Reusable Device Validation (Cleaning Studies) Develop and Coordinate Profiling Protocols Develop Equipment Validations (steam, dry heat, incubators Documentation of all test procedures and validations Provide guidance to other non-exempt personnel within/outside the department | 1/18/2024 |
| 3348 | Companion Medical Bedford, MA Quality Engineer I Bachelors degree required. Exp: 0 years |
In this exciting role as a Quality Engineer I in the Bedford/Billerica facilities, you will have responsibility for supporting the quality and daily manufacturing of high-quality and complex catheters to support the Cardiac Ablation Solutions Business. In this role you will be part of a team that grows the operations capacity over 8X to support our customer needs in this newly acquired product portfolio. You will lead improvements in manufacturing quality, capacity, and stability through solving problems, developing solutions, and executing strategies. | 1/18/2024 |
| 3349 | Companion Medical Rice Creek, MN Quality Engineer I Bachelors degree required. Exp: 0 years |
In this exciting role, the Quality Engineer I will have responsibility for products built at Rice Creek Pharma Operations manufacturing site. Manufacturing Platform East employs the full breadth of our talent, technologies, products, services, and solutions to address the needs of customers and patients across the globe. The Manufacturing East Platform offers devices and therapies to treat abnormal heart rhythms, as well as cardiac diagnostic and monitoring solutions. Rice Creek Pharma Operations, or Fridley, offers devices within the defibrillation solutions, surgical infection control, and diabetes management portfolios. | 1/18/2024 |
| 3350 | Companion Medical Rice Creek, MN Software Engineer I Bachelors degree required. Exp: 0 years |
We are currently seeking a passionate Software Engineer I to join our Advanced Manufacturing Engineer (AME) Team. The Software Engineer I will support the design, development, and validation of Non-Product Software to support the automation and software integration operations for the development and commercialization of new combination devices (device/drug) | 1/18/2024 |
| 3351 | Companion Medical Plymouth, MN Manufacturing Engineer I Bachelors degree required. Exp: 0 years |
Engineers are indispensable to achieving our Mission. That’s why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship, and the guidance you need to continue to develop your expertise. Today, we’re partnering across the industry to confront systemic healthcare challenges – this requires bold leadership. If you want a challenging, energizing, rewarding career that changes lives, join us. We are currently hiring a Manufacturing Engineer I at our Plymouth, MN site. Make an impact on your community and the lives of others by leading sustaining efforts of cutting-edge medical devices. This Engineer would be responsible for first shift technical support of Cardiac Surgery product such as mechanical heart valves. Cardiac surgery represents end-state treatment in the care continuum for many cardiovascular diseases. There are approximately 1.8 million cardiac surgical procedures in the world on an annual basis. Cardiac surgery remains extremely important in treating complex disease and remains the gold standard on which many of the other therapies being developed in Cardiovascular are based upon. | 1/18/2024 |
| 3352 | Cook Biotech Winston Salem, NC Research and Development Engineer 2 Bachelor's degree in Engineering/Technology is required. Exp: 1-2 years |
The primary purpose of the Research and Development Engineer at Cook Winston-Salem is to design, test and technically document the feasibility, construction and production process of new and/or changed medical products. | 1/18/2024 |
| 3353 | Cook Biotech Winston Salem, NC Research and Development Engineer 1 Minimum four year degree in Engineering/Technology. Exp: 0+ years |
The primary purpose of this position is to design, test and technically document the feasibility, construction and production process of new and/or changed medical products. | 1/18/2024 |
| 3354 | Cook Biotech Bloomington, IN Manufacturing Engineer 1 Bachelor’s degree in Engineering or related field. Exp: 0 - 3+ years |
Responsible for providing technical support for the day-to-day production activities in the manufacture of custom, plastic components used in the assemblies of various medical devices. This is a hands-on position with visibility on the manufacturing floor and requires a high level of interaction with the production, product development, and quality teams. The engineer is responsible for supporting product development activities, continuous improvement, complaint resolution, CAPA investigations and other quality initiatives. | 1/19/2024 |
| 3355 | CordenPharma Boulder, CO QC Analyst - Nights Bachelor's Degree (BA) from 4-year college or university. Exp: 0 - 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training Manual. Maintains a high level of housekeeping and attention to detail. | 1/19/2024 |
| 3356 | Contract Pharmacal Hauppauge, NY Microbiologist; Quality Control Bachelor’s degree in a science related field. Exp: 1 - 9 years |
The Microbiologist is responsible for and has experience in performing microbial analysis for the QC Microbiology laboratory which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 1/19/2024 |
| 3357 | Contract Pharmacal Hauppauge, NY Scientist I; Analytical R&D Bachelor’s or Master’s degree in chemistry or analytical chemistry. Exp: 1-2 years |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. | 1/19/2024 |
| 3358 | Contract Pharmacal Hauppauge, NY Lab Tech Associate degree. Exp: 1+ years |
The Laboratory Technician has primary responsibility for conducting basic routine lab analysis and maintaining all laboratory equipment, chemicals, and logbooks per CPC SOPs. | 1/19/2024 |
| 3359 | Crown Bioscience San Diego, CA Research Associate I - Biomarker & Diagnostic Tech Bachelor of Science degree or above in biotechnology, cell biology, immunology, oncology or other related disciplines. Exp: one year |
The purpose of the Research Associate I position is to provide support on biomarker discovery studies to meet company's goals, objectives and quality standards. | 1/19/2024 |
| 3360 | Crown Bioscience San Diego, CA Research Associate I - Cell Culture Technician Bachelor's degree in Biology, Biochemistry or related area. Exp: 1-2 years |
The purpose of the Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 1/19/2024 |
| 3361 | Cyprotex Framingham, MA Research Assistant BA/MS or equivalent experience in a relevant Biological or Chemical scientific discipline. Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro ADME/Tox assays and maintaining mammalian cells. Training opportunities will be provided for high throughput screening, mammalian cell culture and LC-MS/MS. Some cell culture and LC-MS experience are preferred. | 1/19/2024 |
| 3362 | Cyprotex Framingham, MA Research Associate BS/ MS in a relevant bio scientific discipline. Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays. | 1/19/2024 |
| 3363 | Cytovance Biologics Oklahoma City, OK AD Associate II MS in a life science field. Exp: 1+ years |
The AD Associate I/II position develops, optimizes, and qualifies analytical methods for biopharmaceutical products. The associate also supports drug development departments, such as Purification Department and Cell Culture Department, by performing analytical testing. | 1/19/2024 |
| 3364 | DiaCarta Richmond, CA Research Associate Sc. degree in molecular biology or a related field OR S. degree in molecular biology or a related field. Exp: Sc.: 0-1 years; S.: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 1/19/2024 |
| 3365 | DiscGenics Salt Lake City, UT Lab Calibration Technician Bachelors in Biological, Biochemical, or Chemistry related field. Exp: 1-2 years’ |
The Lab Calibration Technician is responsible for inspection, calibration, verification and maintenance of all laboratory equipment to meet established conformance standards. The Lab Calibration Technician will be responsible for performing routine maintenance according to the maintenance schedule or coordinating with external vendors or in-house experts to complete all tasks on time. The role may also be required to perform or coordinate non-routine repairs or calibration to ensure equipment is performing to internal standards. This role interacts with all levels of the organization in a collaborative and positive way with colleagues to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. | 1/19/2024 |
| 3366 | Distributed Bio Seattle, WA Research Associate I B.S. in either animal science or similar discipline preferred. Exp: 6-12 months |
In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). The Research Associate will be responsible for accurate data entry. To ensure the success of the research projects, it is critical that you maintain accurate study records and assist in maintaining lab and facility inventories. As part of your role, you will be expected to complete study reports and perform routine animal health-related tasks such as changing cages or supplying food as needed. Your attention to detail and ability to follow procedures carefully will be essential to ensure the accuracy and reliability of your research results. Lastly, you may need to perform health rounds and treatments on weekends, holidays, and occasional evenings. | 1/19/2024 |
| 3367 | Distributed Bio S. San Francisco, CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
In this role you will observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. You will handle routine handling, restraint, identification (including ear notching, tagging) and sexing of common laboratory animals. Ability to distinguish various common laboratory animal strains in accordance with standardized genetic nomenclature and phenotype identification. You will also perform technical functions required by research protocols such as assist with dilution and dosing calculations; dosing administrations (PO, SQ, IP, IM, and IV); blood collections (Submandibular, Cardiac); basic necropsy and tissue collection; tumor measurement and body weights. Assist Vet Techs and Veterinarians with follow-up checks, treatments and procedure if needed. Perform health surveillance sample collection procedures. Actively interact with research staff to provide technical assistance. | 1/19/2024 |
| 3368 | Distributed Bio Spencerville, OH In Vivo Technician II Associate (A.A./A.S.) or Bachelor’s degree (B.A./B.S.). Exp: 6 months |
We are seeking an In Vivo Technician II for our In Vivo Team at our Safety Assessment site located in Spencerville, OH. A Technician II is performing basic tasks and procedures within a team. The technician is assigned to work on study, performing and becoming more efficient in tasks required of the department training plan which may include collecting and recording data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. The technician is usually working closely with a trainer or buddy but becoming more independent | 1/19/2024 |
| 3369 | Distributed Bio Memphis, TN Biomanufacturing Technician I - Shift C Tuesday-Friday: 11:30am-10:00pm AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
NOTE: This position is: Shift C: Tuesday thru Friday 11:30am - 10:00pm (Saturday, Sunday, Mondays off) The BioManufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 1/19/2024 |
| 3370 | Distributed Bio Newark, DE Molecular Technologist-1 Sequencing Associates Degree in Microbiology or related discipline required. Bachelors Degree preferred. Exp: 0-3 years |
Charles River Labs is seeking a Molecular Technologist for our Microbial Solutions site located Newark, DE. This position is Monday - Friday 10:00am to 6:30pm. The Molecular Technologist 1 will process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping. Ensure adherence to regulatory requirements and GMP compliance. | 1/19/2024 |
| 3371 | Distributed Bio Memphis, TN Biomanufacturing Technician I - Shift A Sun - Wed 7:30am - 6:00pm 1 AS or BS in a scientific field required. Exp: Zero to 1 year |
The Biomanufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to meet physical requirements established in this job description. The hours are as follows: Shift A: Sun – Wed, 7:30am – 6:00pm (Thursday, Friday and Saturdays off) | 1/19/2024 |
| 3372 | Distributed Bio Ashland, OH Technician II, Formulations Bachelor’s degree (B.A./B.S.) in a relevant field. Exp: no experience |
A Technician II will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight. Hours for the position are 9:00am-5:30pm Mon -Fri with potential overtime and/or weekend work. | 1/19/2024 |
| 3373 | Element Biosciences San Diego, CA Research Associate, Surface Chemistry Bachelor’s degree in chemistry, materials science, biochemistry, bioengineering, physics, or similar fields. Exp: 0-2 years |
We are seeking a Research Associate, who has a curious mind and a great desire to learn new techniques in new areas of study to join our interdisciplinary research team. You will be learning experiment design pertaining to surface coating characterization assays, explore optimal surface coating process and support custom surface production needs. The preferred candidate will have scientific research lab experience, demonstrated by any combination of prior curricular, extracurricular undergraduate research lab work, scientific paper, poster, or presentations. | 1/19/2024 |
| 3374 | EMD Serono Kankakee, IL Process Engineer Bachelor’s degree in Biology, Chemistry, or other Scientific discipline. Exp: 1+ years |
MilliporeSigma in Kankakee, IL is hiring a Process Engineer. In this role, you will identify KPIs to enhance processing and efficiencies. You will also assess new technologies to enhance production capabilities as well as reduce variation within the processes. | 1/19/2024 |
| 3375 | EMD Serono Sheboygan Falls, WI Associate Quality Control Chemist (Laboratory) Bachelor's Degree in chemistry, biochemistry,?chemical engineering or other life science discipline. Exp: 1+ year |
The Associate Quality Control Chemist will perform routine assignments using existing procedures and evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 1/19/2024 |
| 3376 | EMD Serono St. Louis, MO Associate Quality Scientist Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other life science discipline. Exp: 1+ year |
Within the Life Sciences division of Millipore Sigma (CTDMO), the Associate Scientist (QC) position will perform quality control activities in support of GMP products at our Cherokee site. The position is within the Analytical Testing team. The job responsibilities include analytical testing and other activities in support of GMP manufacturing. The position will report to the QC Supervisor. | 1/19/2024 |
| 3377 | EMD Serono St. Louis, MO Associate Quality Scientist Bachelor's Degree in Cemistry, Biochemistry, Biology, or other life science discipline. Exp: 1+ years |
As an Associate Quality Scientist, you will be responsible for reviewing the documentation and data generated for analysis of GMP products at our Cherokee site. This review may include data supporting raw materials, in-process, and/or final products. You will be responsible for verifying that documentation and raw data meet good documentation requirements, are technically acceptable, all calculations are appropriate, and specifications are met. Additional expectations may include the review of new or updated procedures for both technical soundness and allowance for appropriate documentation. Review of audit trials, data integrity and GDP. Shift: Monday-Friday 2:00PM to 10:30PM. | 1/19/2024 |
| 3378 | EMD Serono St. Louis, MO Analytical Scientist Master’s Degree in Chemistry, Biochemistry, Engineering, or other scientific discipline. Exp: 1+ years' |
MilliporeSigma is looking for an Analytical Scientist to add to the team at our Cherokee site. In this role, you’ll be working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma. This role will serve as an individual contributor in the Process and Analytical Development organization. You will be involved in working in a lab setting on analytical method development and optimization for external customers in the field of Antibody Drug Conjugates (ADC). The role will require problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations. This role will be reporting to Rodney Zollars. | 1/19/2024 |
| 3379 | EMD Serono St. Louis, MO Analytical Scientist Master’s Degree in Chemistry, Biochemistry, Engineering, or other scientific discipline . Exp: 1+ years' |
MilliporeSigma is looking for an Analytical Scientist to add to the team at our Cherokee site. In this role, you’ll be working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma. This role will serve as an individual contributor in the Process and Analytical Development organization. You will be involved in working in a lab setting on analytical method development and optimization for external customers in the field of Antibody Drug Conjugates (ADC). The role will require problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations. This role will be reporting to Robert Guilmett. | 1/19/2024 |
| 3380 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - 12 Hour Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, or other life science discipline. Exp: 1+ years |
The Associate Production Scientist at MilliporeSigma will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 1/19/2024 |
| 3381 | Endo Pharmaceuticals Rochester, MI Microbiologist II Master of Science degree in microbiology, biology or related field. Exp: 1+ year’ |
Performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 1/19/2024 |
| 3382 | Foxx Life Sciences Londonderry, NH Product Manager Lab, must be local Bachelor’s Degree in an appropriate Engineering discipline such as Mechanical, Biomedical or Chemical Engineering. Exp: 1 – 3 years |
POSITION SUMMARY: The product manager will interact with sales, marketing, Engineering and Leadership teams to provide strategic oversight to develop, launch, and grow new product offerings and solutions. Product manager works in a fast-paced environment. They are organized, can dynamically prioritize short-term and long-term business needs and are driven to work at the intersection of science and business. | 1/19/2024 |
| 3383 | Frenova Renal Research Ogden, UT Biocompatibility Engineer I Bachelor's Degree in related Engineering or scientific discipline required Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 1/19/2024 |
| 3384 | Fresenius Kabi Melrose Park and Chicago, IL Scientist I Possess a B.S. in Chemistry, Biology or related physical science. Exp: 1-4 years |
The Scientist I is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Independently executes protocols, verifications, method transfers in support of senior level personnel. Directs and provides guidance to associate scientists. | 1/19/2024 |
| 3385 | Fresenius Kabi Melrose Park and Chicago, IL Scientist I Possess a B.S. in Chemistry, Biology or related physical science. Exp: 1-4 years |
The Scientist I is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Independently executes protocols, verifications, method transfers in support of senior level personnel. Directs and provides guidance to associate scientists. | 1/19/2024 |
| 3386 | Fresenius Kabi Melrose Park and Chicago, IL Associate Scientist (Nights) BS/BA degree in Science or related field. -or- AS/AA degree. Exp: BS: 0+ years; AS: 1-3 years |
The Associate Scientist is responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Reports testing results and documents in compliance with cGMP and GLP standards. Provides support to Scientist, Lead Scientist, and Supervisor. Prepares media, reagents, sanitizing solutions and equipment for use in testing. | 1/19/2024 |
| 3387 | Bio-techne Minneapolis, MN Quality Assurance Specialist B.S degree in Biology related disciplines. Exp: 0 to 5 years |
The responsibilities of this position are to engage and support various improvement projects for Document Control (Label design and document writing, routing, approval etc) and Quality Assurance activities, including but not limited to Supplier Management, Non-Conformance, CAPA and Change Management etc. | 1/8/2024 |
| 3388 | Bio-techne Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 1/8/2024 |
| 3389 | Bio-techne Minneapolis, MN Quality Technician, Hematology QC Lab MLT/MLS degree, bachelor’s degree in biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, basic troubleshooting, and operation of Hematology analyzers. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to set up and test product on all laboratory instruments and troubleshoot as necessary within 12 months of hire. This position will adhere to safety regulations. Understand the basic ISO protocols and other applicable standards. Perform additional duties as assigned. | 1/8/2024 |
| 3390 | Bio-techne Minneapolis, MN Advanced Research Associate, QC Bioassay Master’s degree om the biological sciences or equivalent. Exp: 0 to 2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires experience with ELISAs, PCR, Western Blotting, and cell culture, including maintenance of cell lines and isolation of primary cells for use in the bioassays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 1/8/2024 |
| 3391 | Bio-techne Minneapolis, MN Advanced Research Associate Bachelor’s degree in Biology, Biotechnology, Biochemistry or equivalent. Exp: 0 to 2 years |
In this position you will build custom made-to-order kits for our rapidly growing Luminex product line, including qualification of assay components, formulation of intermediates, and preparation for packaging. | 1/8/2024 |
| 3392 | Bio-techne San Jose, CA Process Engineering Technician - Instruments Associate degree or equivalent in a relevant technical field (e.g., electrical engineering, mechanical engineering, or similar). Exp: Entry |
We are seeking a skilled and detail-oriented Process Engineering Technician to join our team. In this role, you will be responsible for supporting the development, testing, and maintenance of complex electro-mechanical instruments used in our manufacturing processes. Your expertise will be crucial in ensuring the efficient operation and optimization of these instruments, contributing to the overall success of our organization. | 1/8/2024 |
| 3393 | Bio-techne Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 1/8/2024 |
| 3394 | Camber Spine King of Prussia, PA Associate Project Engineer Bachelor’s degree in Mechanical Engineering (preferred), Biomedical Engineering, or other relevant technical discipline. Exp: 0-3 years |
The Associate Project Engineer will be involved with legacy and new product projects, including project planning, execution, while adhering closely to project timeline and budget. | 1/10/2024 |
| 3395 | Cambrex Marlborough, MA Clean Room Analyst - Microbiological Environmental Monitoring Entry Level: Associate’s degree in Microbiology or related field; Expert Level: Bachelor’s degree or higher in Microbiology or related field. Exp: 12 months |
Our Clean Room Services team is looking for both entry level and veteran Environmental Monitoring Analysts that are passionate about leveraging their talents to provide an outstanding customer experience. If you’re interested in receiving excellent training and working as part of a team of experts with opportunities for growth, you’ll be a great fit in our strong company culture. As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 1/10/2024 |
| 3396 | Advanced Sterilization Products Malvern, PA Associate Scientist, Bioassay Methods Development Master’s degree in Biology, Pharmacology. Immunology, Biochemistry or a related scientific discipline is preferred. Exp: 1 year |
The Associate Scientist, Bioassay Methods Development, will be responsible for the development of cell-based bioassays and binding assays to be used as Quality Control (QC) potency assays and in support of structure-function and biological characterization studies, to better understand mechanism of action for new molecular entities in clinical development and for commercial products. The individual will be accountable for method development, qualification, validation and transfer activities as well as the evaluation of new technologies. | 1/10/2024 |
| 3397 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Solid Tumor (2nd & 3rd Shift) Bachelor’s degree in a science related field. Exp: Less than 1 year |
The Molecular Technologist is responsible for performing various molecular techniques that include, but are not limited to, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, DNA methylation analysis, equipment maintenance, laboratory inventory, sample tracking, ordering supplies and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 1/11/2024 |
| 3398 | Caris Life Sciences Phoenix, AZ Technician - Digital Pathology Operations Associate degree with preferred major in Biological and/or Physical Sciences: or, an equivalent combination of education and experience. Exp: 1+ years |
The technician is responsible for the overall slide-scanning functions of the clinical laboratory including the routine operation and basic troubleshooting of the Whole Slide Scanners, retrieval of glass slides to be digitized, QC by visual inspection of the generated Whole Slide Images, and the testing of new software solutions to support the department. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 1/11/2024 |
| 3399 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Liquid Profiling Bachelor’s degree in a science field is required. Master’s degree in a science field is preferred. Exp: 1+ years |
The Molecular Technologist – Liquid Profiling is responsible for performing various molecular techniques that include, but are not limited to, blood processing and buffy coat extraction, RNA/DNA extractions, PCR, DNA methylation analysis, Next-Generation Sequencing, equipment maintenance, laboratory inventory, sample tracking and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 1/11/2024 |
| 3400 | Catalog Boston, MA Associate Computational Biologist, R&D – Future Technologies B.S. or M.S. in computational biology, molecular biology, biomedical engineering, or a related discipline. Exp: 1+ years |
CATALOG, a Boston-based pioneering startup, is making significant strides in the field of data storage and computation by harnessing the power of DNA. DNA, known for its millennia-long stability, unrivaled information density, and cost-effective replicability, offers revolutionary potential for latency-tolerant high-density data storage and massively parallel computation. We're seeking a motivated Associate Computational Biologist with an interest in synthetic biology to join our interdisciplinary team and contribute to the development of CATALOG's DNA-based data storage and computation platform. | 1/11/2024 |
| 3401 | Catalog Boston, MA Research Associate or Senior Research Associate, DNA Computing BS or MS in biology, molecular biology, biochemistry, or a related discipline. Exp: 1+ years |
We are actively seeking a Research Associate or Senior Research Associate with a solid grounding in molecular biology or chemistry. In this role, you'll be instrumental in helping to build CATALOG's innovative DNA-based data storage and computation platform. You'll collaborate with our dynamic team of computer scientists and biologists, developing novel storage and computing architectures and translating them into scalable chemical operations. Your work will contribute to the optimization of a molecular instruction set that underpins the world’s first DNA storage and computing platform. | 1/12/2024 |
| 3402 | Catalog Boston, MA Research Associate/Senior Research Associate Tech Ops BS or MS in biology, molecular biology, biochemistry, or a related discipline. Exp: 1+ years |
We are actively seeking a Research Associate or Senior Research Associate with a solid grounding in molecular biology or chemistry. In this role, you'll be instrumental in helping to build CATALOG's innovative DNA-based data storage and computation platform. You'll collaborate with our dynamic team of computer scientists and biologists, developing novel storage and computing architectures and translating them into scalable chemical operations. Your work will contribute to the optimization of a molecular instruction set that underpins the world’s first DNA storage and computing platform. | 1/12/2024 |
| 3403 | Cellares South San Francisco, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree or diploma in a scientific or related field is required. Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 1/12/2024 |
| 3404 | Cenetron Diagnostics Milwaukee, WI Tissue Recovery Specialist - Full-time Associate's Degree degree from an accredited college or university in a related healthcare field required. Exp: 1-3 years |
Under the direction of the Supervisor, the Tissue Recovery Specialist (TRS) is responsible for the surgical recovery and acquisition of tissue from donors from referring agencies. | 1/12/2024 |
| 3405 | Cenetron Diagnostics Milwaukee, WI Organ Recovery Specialist - Surgical Tech Associate's Degree or Bachelor’s Degree from an accredited college or university in a related healthcare field required. Exp: 1-3 years |
Under the direction of the Supervisor, Recovery Services the Organ Recovery Specialist is responsible for coordinating, assisting, and performing many of the key aspects related to the surgical recovery process of organ donation. | 1/12/2024 |
| 3406 | Cenetron Diagnostics Indianapolis, IN Associate Technologist Laboratory Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 1/12/2024 |
| 3407 | Cenetron Diagnostics Milwaukee, WI Associate Technologist Laboratory - Molecular Oncology and Genetics Laboratory Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 1/12/2024 |
| 3408 | Cenetron Diagnostics Wauwatosa, WI Research Technologist II - Deininger Lab Bachelor's Degree from an accredited college or university in biology, chemistry or equivalent scientific discipline required. Exp: 1-3 years |
Develops, improves, and implements laboratory techniques and performs complex experiments and/or tests to contribute to the timely and accurate completion of the research project(s). | 1/12/2024 |
| 3409 | Cenetron Diagnostics Milwaukee, WI Technologist Laboratory HLA - $3,500 sign on bonus!!!! Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1-3 years |
Under supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment. Supports the training of junior and peer staff members. Performs higher level interpretation of testing results and test panels. | 1/12/2024 |
| 3410 | Cenetron Diagnostics Wauwatosa, WI Research Technologist - Dr. Dipa Lab Bachelor's Degree from an accredited college or university in biology, chemistry, scientific discipline or equivalent combination of education and exp Exp: 1-3 years |
Under the direction of the Principal Investigator, performs laboratory assays and complex experiments to elucidate novel research questions. | 1/12/2024 |
| 3411 | Champions Oncology Rockville, MD Formulations Technician I BS degree in chemistry, pharmacology, or related field.preferred. Exp: 1 year |
The Formulations Technician will support in vivo oncology research studies in mice. Duties and responsibilities include: Receive, distribute, and disposition test compounds, vehicles, and reagents. Formulate test compounds, vehicles, and reagents. Record study data within the laboratory information management system. Read, understand, and adhere to study protocols. Perform general study preparation and organizational activities, including sample tube labeling, supply organization and stocking, and laboratory organization. Willing to work the following schedule: Friday, Saturday, Sunday, Monday and Tuesday - weekly 11:00am to 7:30pm | 1/12/2024 |
| 3412 | Champions Oncology Rockville, MD Research Associate I, Cell Culture In-Vivo BS degree. Exp: 0- 2 years |
The research associate will perform cross-functional laboratory assays with a focus on in vitro/In vivo studies. Assist in the development and execution of novel assays including collecting and processing data. | 1/12/2024 |
| 3413 | Champions Oncology Rockville, MD Research Technician, Support Team BS degree in animal science, biology, pharmacology, or related field preferred. Exp: 3 to 6 months |
A Research Technician on the Support Team provides general technical support for in vivo oncology studies in mice. | 1/12/2024 |
| 3414 | Champions Oncology Rockville, MD Laboratory Animal Care Technician BS degree in biology, pharmacology, or related field. Exp: 0 - 1+ years |
Support in vivo oncology studies in mice as a member of the Vivarium Operations Team. Duties and responsibilities: Provide animal care including handling, receipt and husbandry procedures Provide animal care including feeding and watering with food and water consumption monitoring Conduct animal observation for general health and overall well-being Clean equipment, rooms and facility according to a schedule devised by senior personnel; including floor sweeping and washing, cage washing and sterilization, and waste removal Document and initial required information in relevant room and log books Material and supply distribution and waste handling Record data using laboratory information management systems | 1/12/2024 |
| 3415 | Champions Oncology Rockville, MD Animal Research Technician I, Study Services BS degree in animal science, biology, pharmacology, or related field. Exp: 1 year |
Support in vivo oncology research studies in mice as a member of the Study Services Team. Duties and responsibilities: Perform in-life technical procedures on mice, including handling, restraint, body weight measurement, tumor volume measurement with calipers or imaging device, compound administration, blood collection, and euthanasia. Record study data within the laboratory information management system. Read, understand, and adhere to study protocols. Perform general study preparation and organizational activities, including sample tube labeling, supply organization and stocking, and laboratory organization. Work weekends and holidays on rotating basis. | 1/12/2024 |
| 3416 | Cisbio Boston, MA Lab Equipment Support Specialist Associates Degree in a Science/Engineering Field or Bachelor’s degree in a Science/Engineering Field. Exp: AS: 1-2 years; BS: 0+ years |
Enhance the existing LAMP infrastructure to track equipment preventative maintenance (PM). Service work will be performed by LAMP/OEMs and customer Facilities engineers. Support System Admin functions Provide the following compliance support activities: Enter all PM and corrective maintenance (CM) service requests and reports in customer logbook (ELN). Confirm each maintenance event receives a signed service report (electronic preferred). Review documents for accuracy. Confirm MS performance checks are done at least monthly, compile results and distribute to staff. Compile service information as needed to support internal QA and agency audits. Manage pipet calibration with record keeping in customer ELN. Generate out of calibration impact memos if there is a pipette calibration failure for customer review and approval. Maintain balance inventory and coordinate with the CUSTOMER MIC centre to support service/calibration report archival by the CUSTOMER assigned personnel. Escalate to customer corporate management if there are issues getting the appropriate support. Confirm Fume hoods/enclosures are PMed on schedule by the customer assigned personnel. Escalate issues to customer’s corporate management. PH meter maintenance – check calibration, electrode storage, and buffer expirations monthly. | 1/12/2024 |
| 3417 | Cisbio Collegeville, PA Chemical Management Specialist Bachelor's degree. Exp: 1+ years |
Performs efficiency studies (assays) and pre-clinical exploratory safety studies. Performs testing of clinical, research and quality control proficiency; evaluates instruments. Evaluates and analyzes clinical research data. Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives. Manages storage of research samples. | 1/12/2024 |
| 3418 | Cisbio Bothell, WA Lab Support Coordinator Associates degree. Exp: 1+ years' |
Serve as point of contact for customer lab staff, facilitating and coordinating laboratory needs and activities. This role will work closely with other teams to seamlessly deliver lab support services. Coordinate the working lab environment daily and oversee all stock items in and near the labs including but not limited to glassware, lab coats, PPE, consumables. Occasionally support / coordinate waste removal from labs, ensuring use of waste streams with appropriate third-party vendors. Act as the liaison for escorting third-party vendors to customer lab staff for maintenance and/or repairs visits. Meet regularly with key stakeholders (lab staff, service providers, management) to identify, review and resolve issues in a timely manner and/or escalate as necessary. Regularly engage with the customer and PerkinElmer staff to ensure quality and compliance within the laboratory. Collaborate with customer line safety reps to ensure a high level of safety is maintained in the lab. Provide updates and timely communication to lab users on service work requests. Provide area walkthrough for new members of customer staff and visitors. Once certified, provide coordination of a 5S (Sort, Set in Order, Shine, Standardize, Sustain) lean service. Required to cross-train and provide back-up to other lab support areas. Complete relevant paperwork according to principles of Good Documentation Practice. Subject Matter Expert (SME) on various support needs across different buildings/floors/locations. | 1/12/2024 |
| 3419 | Coating Place Verona, WI QC Analytical Chemist - FP Team (1st Shift) Bachelor’s degree in Chemistry or related field. Exp: 1+ years |
1st Shift Position 8:00am - 4:30pm, Mon - Fri The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures and conduct analyses with some supervision after training is complete. In addition, support is provided by ensuring the essential job functions of this position are completed as part of the daily and/or weekly schedule. | 1/12/2024 |
| 3420 | Codexis Redwood City, CA Bioprocess Development Downstream Research Associate III Master’s degree in Biochemistry, Biological Science, Chemical or Biomolecular Engineering, or related discipline. Exp: 0-3 years |
The Bioprocess Development Downstream Research Associate III is responsible for designing, performing, and analyzing experiments to establish, understand, and optimize enzyme purification processes. The Research Associate will also be responsible for communicating technical data and contributing to tech transfer activities for external manufacturing of cutting-edge enzymes for nucleic acid synthesis. This position will be based on-site in Redwood City. | 1/12/2024 |
| 3421 | Codexis Redwood City, CA Process Development, Research Associate II BS or equivalent in Chemical Engineering, Biology, Biochemistry or relevant scientific field. Exp: 1 year |
The Process Development Research Associate II will join the Process Chemistry group which is part of the R&D department. Successful candidates will be a part of a dynamic and enthusiastic team responsible for development, scale up and tech transfer of the ECO Synthesis™ platform. The individual will be working with a high performing team with day-to-day laboratory workflows and operations to help with design, optimization, and analysis of ECO Synthesis™ technology. The position is an on-site role located at our Redwood City facility full time. | 1/12/2024 |
| 3422 | Cognate Bioservices Seattle, WA Research Associate I B.S. in either animal science or similar discipline preferred. Exp: 6-12 months |
In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). The Research Associate will be responsible for accurate data entry. To ensure the success of the research projects, it is critical that you maintain accurate study records and assist in maintaining lab and facility inventories. As part of your role, you will be expected to complete study reports and perform routine animal health-related tasks such as changing cages or supplying food as needed. Your attention to detail and ability to follow procedures carefully will be essential to ensure the accuracy and reliability of your research results. Lastly, you may need to perform health rounds and treatments on weekends, holidays, and occasional evenings. | 1/12/2024 |
| 3423 | Cognate Bioservices S. San Francisco, CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking a Research Study Technician I for our Insourcing Solutions Department located in South San Francisco, CA. In this role you will observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. You will handle routine handling, restraint, identification (including ear notching, tagging) and sexing of common laboratory animals. Ability to distinguish various common laboratory animal strains in accordance with standardized genetic nomenclature and phenotype identification. You will also perform technical functions required by research protocols such as assist with dilution and dosing calculations; dosing administrations (PO, SQ, IP, IM, and IV); blood collections (Submandibular, Cardiac); basic necropsy and tissue collection; tumor measurement and body weights. Assist Vet Techs and Veterinarians with follow-up checks, treatments and procedure if needed. Perform health surveillance sample collection procedures. Actively interact with research staff to provide technical assistance. | 1/12/2024 |
| 3424 | Cognate Bioservices Mattawan, MI Research Technician - Pharmacokinetics & Acute Toxicology 1 1 Bachelor’s/Master’s. Exp: 1+ years |
We are seeking an experienced Research Technician for our Pharmacokinetics & Acute Toxicology Team located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 1/12/2024 |
| 3425 | Cognate Bioservices Mattawan, MI Research Analyst I - Immunochemistry Bachelor's degree (BA/BS). Exp: 0+ years |
We are seeking an Research Analyst I for our Immunochemistry at the site located in Mattawan, MI. The following are responsibilities related to the Research Analyst I: The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 1/12/2024 |
| 3426 | Cognate Bioservices Newark, DE Molecular Technologist-1 Sequencing Associates Degree in Microbiology or related discipline required. Bachelors Degree preferred. Exp: 0-3 years |
Charles River Labs is seeking a Molecular Technologist for our Microbial Solutions site located Newark, DE. This position is Monday - Friday 10:00am to 6:30pm. The Molecular Technologist 1 will process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping. Ensure adherence to regulatory requirements and GMP compliance. | 1/12/2024 |
| 3427 | Bausch & Lomb Greenville, SC Microbiology Technician III 2nd Shift BS in Biology, Microbiology or related life science. Exp: 1+ years |
Execute microbiological testing in support of but not limited to Environmental/Water/Bioburden monitoring, Media and lab supplies preparation, Sterility Testing and Microbial Identification. Conducts tests for in-process and finished products as well as raw materials using aseptic techniques. Compliance with all applicable procedures and practices to include local and global SOP’s, product test procedures, safety, USP, ISO, GMP, and applicable governmental regulations. | 1/2/2024 |
| 3428 | Bausch & Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science required. Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 1/2/2024 |
| 3429 | Bausch & Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science required. Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 1/2/2024 |
| 3430 | Bausch & Lomb Rochester, NY Lab Technician IV AAS in Chemistry, or related field. Exp: 1-5 years |
Monitor product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 1/2/2024 |
| 3431 | Bausch & Lomb Rochester, NY Chemist I BS in Chemistry, or related field. Exp: 1-3 years |
The Chemist is a member of the Global Quality organization. This person is responsible to monitor product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 1/2/2024 |
| 3432 | Bausch & Lomb Tampa, FL Chemistry Technical III B. S. in Chemistry preferred, Minimum B.A. in Chemistry or related science. Exp: 1-3 years |
Perform pharmaceutical GMP wet chemistry and instrumental analysis of raw material, in-process, finished product and stability samples in the quality control chemistry laboratory in accordance with all applicable FDA/EP/JP regulations. Assume the responsibility for the GMP, ISO, and Environmental Health and Safety procedure awareness, and compliance within the respective area. | 1/2/2024 |
| 3433 | Bausch & Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science required. Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 1/2/2024 |
| 3434 | Baxter Round Lake, IL Quality Lab Associate I - Stability Bachelor’s degree in Chemistry or biological science with analytical chemistry laboratory coursework. Exp: 0-1 years’ |
The position may be responsible for analytical testing, validation/verification, and/or transfer of test methods supporting parenteral products. The position will be in the Round Lake, IL Stability Laboratories within Product Quality serving multiple global businesses. This role is essential for supporting the global commercial product teams and/or product development teams. The position may collaborate with multiple functions. The individual in this position must: 1) Optimally demonstrate working technical knowledge and skills to support a variety of projects within the relevant discipline with minimal assistance. 2) Display basic technical understanding of related teams. 3) Conduct routine/ experiments with assistance. | 1/3/2024 |
| 3435 | Baxter Marion, NC Associate I, Quality Lab Master’s Degree in Natural Sciences: Chemistry preferred. Exp: 0-3 years |
Conduct qualitative and quantitative chemical analysis on raw materials, solutions, and components following approved Standard Operating Procedures and test methods in an accurate and timely manner. Ability to work under minimum supervision while meeting deadlines. | 1/3/2024 |
| 3436 | Baxter Marion, NC Quality Associate I - Plastics (8th Shift: 7pm-7am) Bachelor's degree preferred. Exp: 0+ years |
Responsible for providing Quality support and oversight via direct staff supervision or process/area responsibilities. Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Baxter quality practices. | 1/3/2024 |
| 3437 | Baxter Marion, NC Quality Lab Associate I - Micro ID B.S. degree in Microbiology, Biology, or related science. Exp: 0-2 years |
Responsible for reading plates for EM, Bioburden, and special project testing and recording test results. Performs additional microbiological testing as required. | 1/3/2024 |
| 3438 | Baxter Marion, NC Quality Associate I (3rd Shift: 10pm-7am) Bachelor's degree strongly preferred. Degree in engineering or life science preferred. Exp: 1+ years |
Responsible for working with the manufacturing departments to address defects with the finished products. | 1/3/2024 |
| 3439 | Baxter Marion, NC CAPA Associate I Bachelor's degree preferred(in science or engineering preferred). Exp: 1+ years |
Will be an Investigation Owner and/or CAPA Owner and is responsible for developing and performing the investigation, identifying the root cause(s) of the event, and detailing the results of the investigation. The CAPA I will likely assist in identifying the appropriate actions to mitigate or eliminate the root causes, and in determining an Effectiveness Plan for the actions (including efficiency criteria and timeframe). | 1/3/2024 |
| 3440 | Baxter Marion, NC Quality Lab Associate II - Endotoxin Master’s Degree in biological sciences. Exp: 0-3 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 1/3/2024 |
| 3441 | Becton Dickinson Tempe, AZ Manufacturing Engineering II Master’s degree in a technical field. Exp: one to three years |
This is a manufacturing engineering position for the Vascular Graft and Covered Stent Graft production facility. This position is responsible for development of process improvements and validations of Vascular Graft and covered Stent Graft production processes. This position is also responsible for the transfer of newly developed products to production. | 1/3/2024 |
| 3442 | Becton Dickinson Columbus, NE Manufacturing Unit Process Engineer Bachelors Degree in an engineering discipline or equivalent experience. Exp: no experience |
This position is responsible for supporting the manufacturing operation. This individual will develop and implement improved methods of manufacturing, procedures, and processes that result in improved efficiencies, yields, machine operations, and quality. Provides technical support to the development group for the implementation of new products or processes. | 1/3/2024 |
| 3443 | Becton Dickinson Grayson; Covington, GA Microbiology Lab Tech BS in Biological Science. Exp: 1-3 years |
The Laboratory Technician is responsible for manufacturing various bacterial antigens, antisera, Treponema product line, Myco product line, Bactrol product line, purified proteins and various solutions including but not limited to buffers, reagents growth media etc. to the finished bulk product stage. | 1/3/2024 |
| 3444 | BeiGene Hopewell, VA Purification,Technician I AS/BS/BA in science related field. Exp: 1+ years |
The Purification Manufacturing Technician I position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. | 1/3/2024 |
| 3445 | BeiGene Hopewell, VA Cell Culture, Technician II AS/BS/BA in science related field. Exp: 1+ years |
The Cell Culture Manufacturing Technician II position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. | 1/3/2024 |
| 3446 | Berg Framingham, MA Research Associate Bachelor’s degree in Biology, Chemistry, Biochemistry, or a closely related field of study. Exp: One (1) year |
Assist in ligand binding assay method development (MSD, ELISA) and provide technique and application support for immunoassays transferred to downstream users. Test antibody quality for purity (SDS-PAGE), specificity (Western Blot, ELISA), and concentration (Nanodrop, BCA). Conduct assay performance validation. Perform protein analysis (SDS/native-PAGE, Western Blot, and Immunoprecipitation). Develop experiment protocols and prepare SOPs. Perform laboratory experiments carefully and troubleshoot to solve problems. Meticulously document experiment results in laboratory notebooks and databases timely. Analyze, summarize, and present experimental results to managers and other team members. Prepare experiment and project reports as required. Order and stock laboratory supplies for a continuous and consistent workflow. | 1/4/2024 |
| 3447 | Bethyl Laboratories, Inc. Montgomery, TX Lab Associate BS, Bachelor of Science, or related degree. Exp: 1+ years |
In this position you will support all company mammalian cell culture needs, including both production and research and development, in support of our antibody development activities. In this position you will assist with all tasks in the cell culture core. These include, but are not limited to, maintaining cells and carrying out transient transfections for expression and purification of recombinant proteins and antibodies; culturing hybridoma cell lines for antibody production; and maintaining a cell bank of over 125 different human and rodent cell lines, processing them for flow cytometry, FFPE cell pellets and cell lysate. The successful candidate is detail-oriented, highly motivated, and willing to learn new skills. Bethyl Laboratories is nimble, market-focused and growing. If you are looking for the opportunity to be first, fast, and flexible, come join us! | 1/4/2024 |
| 3448 | BGI San Jose, CA LC/MS Research Associate - Small Molecule B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
San Jose Mass Spec Lab of BGI Americas is seeking an exceptional and motivated research associate with competitive compensation. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up metabolomics and lipidomics capability in SJMS lab, 4) to support other departments when needed. A candidate with metabolomics/lipidomics LC-MS experience is a plus; a candidate with small molecule sample prep experience is a plus. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for metabolomic or lipidomics analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and working with biofluids is a plus. | 1/4/2024 |
| 3449 | BGI San Jose, CA LC/MS Research Associate - Proteomics B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
BGI Americas San Jose Mass Spec (SJMS) center is seeking an exceptional and motivated research associate to join our Proteomics department at our San Jose facility. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up additional proteomics capability in SJMS lab, 4) to support other departments when needed. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for proteomics and biologics characterization analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and, working with biofluids is a plus. | 1/4/2024 |
| 3450 | BioFire Diagnostics Hazelwood, MO Mechanical Engineer Master’s Degree in Mechanical Engineering. Exp: 1+ year |
Assists in the definition, proof of concept, development, implementation and/or support of technical or business solutions by performing specific tasks within the scope of the assigned activity. Identifies issues and uses problem-solving tools to formulate the necessary activities to provide successful solutions. Ensures quality of deliverables by following the appropriate design practices and departmental procedures for design control and regulatory compliance. Creates appropriate documentation such as technical communications, reports, meeting notes and other relevant technical documentation within the role’s function. Prioritizes activities within the scope of the assignments to ensure schedules or quality of work is successfully achieved. Ability to define, review and check product Bill of Materials (BOM) structures, assembly instructions and test procedures. Works with internal department and project specific teams | 1/4/2024 |
| 3451 | BioFire Diagnostics Hazelwood, MO Lab Technician - Media Tech Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 1/4/2024 |
| 3452 | BioFire Diagnostics Salt Lake City, UT Laboratory Technologist - QC I/II Associate degree or higher in a Life Science or related field. Exp: Technologist I - 6 months |
QC Technologist I works in a cGMP environment performing quality control testing for commercial and diagnostics products. Responsibilities include conducting testing of reagents and IVD materials as well as personnel swabs. Responsibilities include working with Manufacturing, Technology Transfer and other departments for data collections and validations for new product QC qualifications, organization of quality-controlled materials used for QC testing and learning new techniques or workflow as required by new product lines. QC Technologist I is also responsible for gathering and filling out quality documents pertaining to quality control testing, generation of Non-Conformance Report (NCR) when necessary and Temporary Change Order (TCO) application. QC Technologist II will be responsible for software-assisted product release (e.g., Pouch QC Web releases). This position will work in a laboratory setting and perform a variety of scientific techniques, including spectrophotometry, PCR, pipetting, etc | 1/4/2024 |
| 3453 | BioFire Diagnostics Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. The LT-I will receive general instruction on routine work, perform lab duties under supervision, and receive training and additional instruction for new tasks as needed. | 1/4/2024 |
| 3454 | BioFire Diagnostics Salt Lake City, UT Lab Technologist I - Oligo, Night Shift Bachelor’s Degree (BS), or working toward a degree. Chemistry, BioChemistry, and Biology preferred. Exp: 1+ years |
***SIGN ON BONUS OFFERED*** $500 on first paycheck $500 after 6 months of employment BioMerieux is seeking a Lab Technologist I to join our swing shift team that manufactures Oligonucleotides. Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments. | 1/4/2024 |
| 3455 | BioFire Diagnostics Salt Lake City, UT Research Associate I Bachelor's degree in a scientific discipline. Exp: six months' |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and bioMérieux. A Research Associate I may receive general or detailed instruction and direct supervision on general work, new procedures, and assignments | 1/4/2024 |
| 3456 | BioFire Diagnostics Salt Lake City, UT Lab Technologist I - Oligo, Day Shift Bachelor’s Degree (BS), or working toward a degree. Chemistry, BioChemistry, and Biology preferred. Exp: 1+ years |
Sunday - Tuesday from 6:00 AM - 6:00 PM + every other Wednesday Thursday - Saturday from 6:00 AM - 6:00 PM + every other Wednesday ***SIGN ON BONUS OFFERED*** $300 on first pay check $300 after 6 months of employment We are seeking a Lab Technologist I to join our team. Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments Strong pipetting skills, attention to detail, organization, and familiarity with cGMP are desired. | 1/4/2024 |
| 3457 | Biogen Research Triangle Park, NC Associate II, QC Microbiology B.S. Degree. Exp: 1 1/2 - 2 years |
Schedule: this position will work 4-day, 10-hour shift Friday-Monday from 8 AM to 6 PM. The Associate II, Quality Control is responsible for supporting key functional, tactical, and operational aspects of the QC Microbiology group at the Biogen manufacturing facility. | 1/4/2024 |
| 3458 | Biogen Research Triangle Park, NC Manufacturing Associate III Bachelor’s Degree (STEM preferred). Associate’s Degree. Exp: BS: 6 months; AS: 1 year |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling area, and our teams operate across the following units: | 1/4/2024 |
| 3459 | Biogen Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred) OR Associate’s Degree OR Military training & experience and are soon to transition. Exp: Entry-Level |
This requisition represents multiple open positions in our RTP Manufacturing organization. The Talent Acquisition team continually assesses all applicants that apply through this posting and will reach out to the selected candidates to discuss current and future opportunities. | 1/4/2024 |
| 3460 | Biogen Research Triangle Park, NC Associate II, QA - Swing Shift Bachelor’s degree preferably in a field of science or biotechnology. Exp: 0-2 years |
The Quality Assurance Associate II is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. Activities include but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identifying gaps in existing Quality systems and proposing solutions to site management. The QA Associate will perform all duties in a manner consistent with site and corporate policies, cGMP, safety, environmental and human resources policies and procedures and also adhere to all regulatory licenses and regulations, interfacing with key Quality and manufacturing customers, and coordination of investigations impacting the RTP site. The QA Associate may participate in internal compliance audits; assess and approve discrepancies from site, corporate, and regulatory guidance. The QA Associate will also ensure compliance with training policies. Please note that this is a Swing Shift position and will work a traditional 2-2-3 Manufacturing Rotation from 12pm to 12am, on a 12hr/shift schedule. There is a 10% pay differential for this position. | 1/4/2024 |
| 3461 | BioLegend Pittsburgh, PA Associate Lab Technologist Bachelor's degree in a life science discipline such as Biology, Chemistry, or Medical Technology. Exp: 0-3 year |
Our team is seeking an Associate Lab Technologist to join us in our efforts to serve patients and families around the world. | 1/5/2024 |
| 3462 | BioLegend Pittsburgh, PA Research Clinical Laboratory Scientist Bachelor’s Degree in life sciences. Exp: 1-2 years |
The research clinical laboratory scientist will assist in the validation and performance of clinical laboratory tests for the diagnosis, treatment, and prevention of disease within humans. | 1/5/2024 |
| 3463 | BioLegend Lafayette, CO Associate Scientist Bachelor's Degree in Life Sciences. Exp: 0-3 years |
Revvity has a rewarding and exciting opportunity for an Associate Scientist for our Synthetic Manufacturing laboratory. The Associate Scientist position will perform primary tasks in an ISO 9001:2015 laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the manufacturing, processing, and packaging of RNA and DNA oligonucleotides. This includes synthesis, cleaving, quality and quantity determination, purification, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry in multiple laboratories. | 1/5/2024 |
| 3464 | LGC Biosearch Technologies Middleton, WI Associate Production Scientist, Comp Cells Associate degree in relevant life sciences field (molecular biology, microbiology, biochemistry, etc.). Exp: 1+ years |
The Associate Production Scientist will manufacture competent cells for the Company’s various product lines. The position may expand to also support manufacture of additional product lines and development of new products, applications and businesses. This position is regularly based out of the company's site in Middleton, WI, with standard hours of operation Monday-Friday (8am-5pm). | 1/5/2024 |
| 3465 | LGC Biosearch Technologies Petaluma, CA Associate Engineer, Facilities Services 4 Year Degree in Mechanical Engineering, Electrical Engineering or similar. Exp: 1+ Year |
The Associate Engineer will function as an integral part of LGC’s Engineering team and will help provide strategic vision and technical support to ensure that the facilities/utilities/equipment for LGC Biosearch’s manufacturing sites are designed and operating efficiently and safely. The primary purpose of this role is to provide engineering support and design expertise for Biosearch’s Petaluma and Novato manufacturing facilities. This individual will be involved in the design and implementation of process improvements and system maintenance. This role will support the design, engineering, commissioning, and qualification of new or modified utility equipment systems and/or GMP manufacturing process instrumentation. | 1/5/2024 |
| 3466 | Biosero San Diego, CA Mechanical Design Engineer Bachelor’s degree in Bioengineering, Mechanical Engineering, or comparable field. Exp: 1 year |
We are looking for driven Mechanical Design Engineer to join our Engineering Team and help us design world-changing laboratory automation systems and associated hardware products. In this role, you will also assist the applications and sales teams in the conceptualization of automation workcells, generate the bill of materials for projects and products, work with the procurement team and vendors to ensure all fabricated components are ordered and tracked, and generate assembly drawings and instructions for the Automation Team to build projects. | 1/5/2024 |
| 3467 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, RNA Synthesis Bachelor’s in Chemistry, Biochemistry, or a related field. Exp: 0-3 years |
· Design, synthesis, purification, and analysis of chemically modified oligonucleotides · Improve upon and/or develop new synthetic methods and processes to expand the current capabilities. · Utilize analytical instrumentation such as UV-Vis spectroscopy, HPLC, and/or LC-MS for the analysis of both crude and purified synthetic products. Effectively troubleshoot synthetic/process issues and independently find solutions. · Improve upon and/or develop new methods and automation for the downstream processing of synthetic oligonucleotides and their subsequent analysis/purification and annealing into siRNA duplexes. · Analyze, interpret, and organize analytical data to present to team members.· | 12/27/2023 |
| 3468 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, Protein Sciences BS/MS degree. Exp: 0-1 years |
We are seeking an associate scientist-II to join our protein sciences group within Medicinal Chemistry to help with production, protein chemical conjugation and development efforts. The candidate must be independent, goal oriented, technically competent, and able to efficiently work across multiple projects. We are searching for enthusiastic, innovative, and highly motivated individuals, with scientific background in protein expression, purification, protein conjugation and analytical techniques, who are comfortable working in a fast-paced entrepreneurial environment. This position is onsite and will be located at 675 W. Kendall St. Cambridge, MA 02142We are seeking an associate scientist-II to join our protein sciences group within Medicinal Chemistry to help with production, protein chemical conjugation and development efforts. The candidate must be independent, goal oriented, technically competent, and able to efficiently work across multiple projects. | 12/27/2023 |
| 3469 | Alphazyme Jupiter, FL Formulation and Order Fulfillment Technician Associates degree in life science discipline such as Molecular Biology, Biochemistry or Biotechnology. Exp: 1+ years |
Maravai LifeSciences is seeking a #MiracleMaker to join our Order Fulfillment team as a Formulation and Order Fulfillment Technician. As a Formulation and Order Fulfillment Technician you will support Alphazyme’s maintenance and production of inventory necessary for fulfilling customer demands, which includes all activities related to maintaining the responsible lab area, and assists with supporting internal demands and the management of relevant formulation and fulfillment processes through executing protocols. | 12/27/2023 |
| 3470 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 12/27/2023 |
| 3471 | Alveo Technologies Alameda, CA Scientist I BA/BS degree in Biochemistry, Molecular Biology, Microbiology or related field. Exp: 1-3 years |
Alveo Technologies is looking for a Development and Verification Scientist I to support ongoing V&V efforts of projects in disease detection. The successful candidate will assist in planning and executing protocols / conducting experiments at the bench to meet objectives. The candidate should be able to review, understand and follow the instructions, protocols and SOPs provided by the R&D and Manufacturing departments. | 12/27/2023 |
| 3472 | Amarex Clinical Research Ann Arbor, MI Lab Technician I Associate’s degree in a physical science. Exp: 1+ years |
NSF is looking for a motivated candidate who enjoys working hands-on and on their feet to be in the Exposures or Preparations Lab as a Technician I. This position is perfect for someone looking to get lab experience and have the potential to learn and grow within a certification company. This role is to perform laboratory procedures in an accurate and timely manner and continue to expand skill base while under supervision. Depending on the circumstance, potential for flexible schedules and/or part-time if someone is in school obtaining their degree and would like this experience. | 12/27/2023 |
| 3473 | Amarex Clinical Research Ann Arbor, MI Lab Technician I Associate’s degree in a physical science. Exp: 1+ years |
NSF is looking for a motivated candidate who enjoys working hands-on and on their feet to be in the Exposures or Preparations Lab as a Technician I. This position is perfect for someone looking to get lab experience and have the potential to learn and grow within a certification company. This role is to perform laboratory procedures in an accurate and timely manner and continue to expand skill base while under supervision. Depending on the circumstance, potential for flexible schedules and/or part-time if someone is in school obtaining their degree and would like this experience. | 12/27/2023 |
| 3474 | AmbioPharm North Augusta, SC Quality Control Chemist I Bachelor’s Degree in Chemistry or life sciences. Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Perform Quality control raw material/ release/ stability testing. Support routine analytical testing using KF, FTIR, UV and HPLC. Adapt, maintain, and operate analytical instrumentation. Perform method transfer and validation activities with minimal supervisor guidance. Conduct all quality QC chemical tests. Involve in procedure review and propose modifications and updates. Conduct various analytical testing procedures as per QC SOPs | 12/27/2023 |
| 3475 | Amide Tech Cambridge, MA Research Associate / Senior Research Associate - Peptide Chemistry BS or MS degree or equivalent experience in chemistry, chemical engineering, biochemistry, or related field. Exp: 1+ years |
Amide is seeking an exceptional individual to join our growing team as a Research Associate/Technician. The successful candidate will be a key contributor to various research projects and be responsible for executing laboratory experiments, analyzing and reporting results, and working within a larger team on a regular basis. Applicants should be team players able to excel in a fast-paced, collaborative environment. | 12/28/2023 |
| 3476 | Amneal Pharmaceuticals Brookhaven, NY Production Engineer Bachelors Degree (BA/BS) Engineering discipline or Master Degree (MS/MA) Engineering discipline. Exp: less than one year |
The Production Engineer plans and designs methods to improve production processes. Reviews existing processes and develops solutions to increase productivity or reduce costs. Ensures compliance with approved production methods and quality standards. | 12/28/2023 |
| 3477 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist I Bachelors Degree (BA/BS) in Chemistry or related field. Exp: 1+ years |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 12/28/2023 |
| 3478 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist I Bachelors Degree (BA/BS) Microbiology or related field. Exp: 1+ years |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 12/28/2023 |
| 3479 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist II Master Degree (MA/MS). Exp: 1+ years |
The QC Chemist II (internally titled “Scientist II, Quality Control”) is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 12/28/2023 |
| 3480 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist II Master Degree (MA/MS) in Chemistry or related science discipline. Exp: 1+ years |
The QC Chemist II (internally titled “Scientist II, Quality Control”) is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 12/28/2023 |
| 3481 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist II Master Degree (MA/MS) in Chemistry or related science discipline. Exp: 1+ years |
The QC Chemist II (internally titled “Scientist II, Quality Control”) is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 12/28/2023 |
| 3482 | AnaSpec Fremont, CA Synthesis Chemist I BS or above in Chemistry, Organic Chemistry, or related disciplines. Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). As a member of the Synthesis department, the Synthesis Chemist I will work closely with the Purification, QC, and Sales & Business Development departments. | 12/28/2023 |
| 3483 | AnaSpec Fremont, CA QC Chemist Bachelor's degree in Chemistry or science related field. Exp: 1+ years |
This position is responsible for performing analytical testing for various product lines, such as peptides, dyes, and unusual amino acids and ensures that the products are evaluated in a timely manner and meet all procedural requirements. | 12/28/2023 |
| 3484 | AnaSpec Fremont, CA GMP Manufacturing Chemist Bachelors in chemistry, organic chemistry, biochemistry. Exp: 1+ years |
The GMP Manufacturing Chemist will be responsible for supporting all GMP upstream and downstream peptide manufacturing related processes. The GMP Manufacturing Chemist will ensure prioritization, and proper documentation of projects. This individual will work closely with GMP downstream lead and GMP upstream lead. The GMP Manufacturing Chemist is also responsible for ensuring that the assigned tasks are completed in a timely manner. | 12/28/2023 |
| 3485 | Ansh Labs Webster, TX Scientist Master’s degree in Biological/Chemical Sciences/Biotechnology or related area. Exp: 1 year |
As a key member of the Manufacturing or R&D Department, this individual will provide critical scientific skills to assist in the development and scale-up of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays, Lateral Flow assays and micro fludics based immunoassays). | 12/28/2023 |
| 3486 | Ansh Labs Webster, TX Jr. Scientist Bachelor’s degree in Biological/Chemical Sciences/Biotechnology or related area. Exp: one year |
As a key member of the Manufacturing, Research & Development and Quality Control departments, this individual will provide critical scientific skills to assist in the development, scale-up and QC testing of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays). | 12/28/2023 |
| 3487 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I Bachelor’s degree in an Engineering or Science, Technology, Engineering, and Mathematics (STEM) field or related education and experience. Exp: 0+ years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. | 12/29/2023 |
| 3488 | Applied Medical Rancho Santa Margarita, CA CAPA Quality Engineer I Bachelor’s degree in an Engineering or Science, Technology, Engineering, and Mathematics (STEM) field or related education and experience. Exp: 0+ years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. | 12/29/2023 |
| 3489 | Argonaut Manufacturing Services Carlsbad, CA Bioprocess Technician II/III Level II: Requires a bachelor's degree in a related field. Exp: 1 year |
The Bioprocess Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% on-site, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. This role is 12:00 pm - 8:30 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. | 12/29/2023 |
| 3490 | Argonaut Manufacturing Services Carlsbad, CA Formulation Technician II/III Level II: Requires a bachelor's degree in a related field. Exp: 1 year |
The Formulations Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% on-site, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. This role is 12:00 pm - 8:30 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance | 12/29/2023 |
| 3491 | Argonaut Manufacturing Services Carlsbad, CA Manufacturing Technician II or III Level II: Requires a bachelor's degree in a related field. Exp: 1 year |
The Manufacturing Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% on-site, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. This role is 12:00 pm - 8:30 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. | 12/29/2023 |
| 3492 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 12/29/2023 |
| 3493 | Artiva Biotherapeutics San Diego, CA Manufacturing Associate (Temporary) Bachelor’s degree in relevant science or engineering discipline. Exp: 1 years |
The Manufacturing Associate will support manufacturing of Artiva’s off-the-shelf cell therapy platforms in our new, state of the art, cGMP facility. The successful candidate will develop, adhere to, and optimize written procedures (SOPs) related to GMP facility operations, monitor equipment and facilities, and will play a key role in the manufacturing of cell therapies internally at Artiva. The ideal candidate will demonstrate in-depth knowledge of cGMP compliance and will be a self-starter and have the ability to work independently to achieve corporate objectives. This is a temporary position and is located at our corporate headquarters in San Diego, CA. | 12/29/2023 |
| 3494 | Astute Medical Salt Lake City, UT Research Associate I Bachelor's degree in a scientific discipline. Exp: six months' |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. | 12/29/2023 |
| 3495 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field, or hold an Associate’s degree and have exceptional lab experience. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 12/29/2023 |
| 3496 | Astute Medical Hazelwood, MO B-Lab Technician - Media Lab Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 12/29/2023 |
| 3497 | Astute Medical Hazelwood, MO Lab Technician - Media Lab Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 12/29/2023 |
| 3498 | Astute Medical Hazelwood, MO Lab Technician-Media Lab Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
This is a 3rd shift position. The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 12/29/2023 |
| 3499 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field, or hold an Associate’s degree and have exceptional lab experience. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 12/29/2023 |
| 3500 | Astute Medical Salt Lake City, UT Lab Technologist I - Oligo, Day Shift Bachelor’s Degree (BS), or working toward a degree. Chemistry, BioChemistry, and Biology preferred. Exp: 1+ years |
We are seeking a Lab Technologist I to join our team. Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments Strong pipetting skills, attention to detail, organization, and familiarity with cGMP are desired. | 12/29/2023 |
| 3501 | Atalanta Therapeutics Boston, MA Associate Scientist II, Oligonucleotide Chemistry Master’s degree in Chemistry or related scientific discipline. Exp: 0-2 years |
Atalanta Therapeutics is seeking a motivated Associate Scientist to join the Chemistry team to assist with the preparation of oligonucleotides for drug discovery. The Associate Scientist will work as part of a team on various projects that are critical in advancing our research and development efforts, using specialized equipment to produce high-quality compounds and analyzing data to facilitate process optimization. This individual will deliver oligonucleotides for research experiments, help maintain and troubleshoot equipment, and collaborate with cross-functional teams in a cutting-edge laboratory environment. Successful candidates will have strong analytical and problem-solving skills with an eagerness to learn and contribute to a dynamic team environment. | 12/29/2023 |
| 3502 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, In Vivo Pharmacology Master’s degree. Exp: 0-2 years |
Atalanta is seeking a highly skilled and motivated Associate/Senior Associate Scientist to join the in vivo pharmacology group to support Atalanta’s drug discovery programs. This individual will have extensive hands-on experience in performing survival surgeries (stereotaxic or direct intraparenchymal injection preferred), pharmacological administration, brain and tissue collection, and in processing CNS tissue and molecular analysis to assess target gene and protein expression. We are seeking candidates who thrive in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The Associate/Senior Associate Scientist will be responsible for assay development and execution of experiments to determine the biodistribution, pharmacodynamic properties and efficacy of oligonucleotides in research and preclinical studies supporting multiple drug discovery programs and platform discovery research. | 12/29/2023 |
| 3503 | August Bioservices Nashville, TN Manufacturing Technician I/II/III - Formulation & Component Prep BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year or more |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician– Component Preparation and Formulation will operate a variety of processing and packaging equipment to prepare components for aseptic filling to include bulk formulation of aqueous and non-aqueous based products, order and receive components, dispense and formulate raw materials, manage sterilized components, operate various equipment used in the formulation process, and perform cleaning operations for process equipment and the GMP ISO 8 areas. | 12/29/2023 |
| 3504 | August Bioservices Nashville, TN Manufacturing Technician I/II/III – Filling, Lyophilization, & Terminal Sterilization BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year or more |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician – Filling, Lyophilization, and Terminal Sterilization will use proper aseptic technique while performing tasks in aseptic manufacturing areas to include syringe and vial filling operations with an automated line in an RABS environment as well as routine and non-routine aseptic interventions through RABS glove ports. The technician II level will operate filling and auto loading equipment, and freeze dryers using automated control systems. The Technician will be responsible for unloading of autoclaves, performing cleaning operations for process equipment and the GMP ISO 8 areas, management of sterilized components, and coordinating with maintenance as needed. | 12/29/2023 |
| 3505 | AxoGen Vandalia, OH QC Histology Technician Associate degree in chemistry, biology, or a science/technical related field required (Bachelor’s degree preferred). Exp: 1+ years |
The Quality Control (QC) Histology Laboratory Technician will support QC Histological testing by conducting a variety of laboratory tasks. He/she will also be responsible for routine laboratory operations including maintenance, solution and media preparation, routine testing, ordering supplies, and laboratory housekeeping. The QC Histology Technician will be required to handle biohazardous materials. The successful candidate will carry out testing and evaluations according to established procedures, document results, and detail any testing observations. He/she may be responsible for incoming materials release, in process testing, and release testing. He/she will also contribute to writing reports and documenting laboratory standard operating procedures (SOPs). The successful candidate will be responsible for cleaning, disinfecting, and managing inventory of lab equipment other related duties as assigned. | 12/29/2023 |
| 3506 | Bardy Diagnostics Plymouth, MN Engineer I - R&D Disposables (Hybrid) BS in Mechanical, Plastics, Biomedical Engineering or a related field, MS preferred. Exp: 0 - 1 year |
What you'll be doing Document engineering concepts. Create, modify, and maintain design documentation per company procedures. Assist in the design and building of basic tooling, test fixtures and assembly equipment. Build prototypes and models and may operate machine tools. Understand customer needs through literature review, customer interviews, direct observation, competitive analysis, prototype evaluation, and clinical/simulated use studies. Write technical reports based on design verification analysis/testing for design changes and product design activities. Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis, and data analysis. Identify, investigate, and solve engineering problems. | 12/29/2023 |
| 3507 | Uptake Medical Johnson City, TN Quality Control Chemist - 2nd Shift Minimum 2-year Associates Degree or 4-year BS Degree in Science. Exp: 0 - 5 years’ |
The QC Chemist 1 is responsible for assisting in supporting Quality Control Laboratory personnel as it pertains to the sampling of raw materials, purified water system, in-process materials and finished products. | 12/18/2023 |
| 3508 | Uptake Medical Johnson City, TN Associate Scientist Bachelor’s degree in Chemistry or other related discipline. Exp: 0-2 years |
Crown Laboratories, Inc. is currently recruiting for an Associate Research Scientist. The Associate Research Scientist is responsible for assisting the Research Scientist and the R&D department in the development of new products from concept to commercialization to support company growth. | 12/18/2023 |
| 3509 | Wugen St. Louis, MO Associate Scientist: CMC Process Development MS Degree in biology or related field. Exp: 1+ years |
Join a fast-paced startup based in St. Louis with the opportunity to help drive process development activities of novel therapies for treating rare diseases. The associate scientist role is part of the CMC department, and will focus on executing experiments in flow cytometry. | 12/18/2023 |
| 3510 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab (1st Shift) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 12/18/2023 |
| 3511 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab (1st Shift) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 12/18/2023 |
| 3512 | Abbott St. Paul, MN Clinical Engineer-2 Associates Degree. Exp: 1 year |
Under general supervision, responsible for designing new products and processes and improving and maintaining existing products. May execute less complex projects. Under general supervision, responsible for designing new products and processes and improving and maintaining existing products. May execute less complex projects. Under general supervision, responsible for designing new products and processes and improving and maintaining existing products. May execute less complex projects. | 12/18/2023 |
| 3513 | Abbott Irving, TX Associate Mechanical Engineer BS Mechanical Engineering. Exp: 0-2 years’ |
Individual contributor that works under limited supervision. Designs mechanical and electromechanical products and systems by developing and testing specifications and methods. | 12/18/2023 |
| 3514 | Abbott Sturgis, MI Assistant Microbiologist I (2nd Shift, Tues-Sat) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
Apply high quality scientific techniques in the microbiological analysis of raw ingredients, in-process production samples, finished product testing and environmental monitoring, to ensure that all products manufactured are fit for use Be able to work with fellow microbiologist, with a high degree of motivation, attention to important details with clear communication to all team members. This is important due to the high degree of responsibility and working within a small group where each person is relied upon highly Prioritize tasks to efficiently be completed with the most accurate results, and to communicate clearly and work together in a team environment Product testing, Environmental testing, Raw ingredient testing Documentation, Project work, Troubleshooting Media preparation/general lab work: Housekeeping Communication, Teamwork | 12/18/2023 |
| 3515 | Abbott Sturgis, MI Assistant Microbiologist I (3rd Shift) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
Apply high quality scientific techniques in the microbiological analysis of raw ingredients, in-process production samples, finished product testing and environmental monitoring, to ensure that all products manufactured are fit for use Be able to work with fellow microbiologist, with a high degree of motivation, attention to important details with clear communication to all team members. This is important due to the high degree of responsibility and working within a small group where each person is relied upon highly Prioritize tasks to efficiently be completed with the most accurate results, and to communicate clearly and work together in a team environment Product testing, Environmental testing, Raw ingredient testing Documentation, Project work, Troubleshooting Media preparation/general lab work: Housekeeping Communication, Teamwork. | 12/18/2023 |
| 3516 | Abbott St. Paul, MN Manufacturing Engineer I Bachelors of Science degree in Electrical Engineering, a related field or equivalent. Exp: 0-3 years |
This position works out of our St Paul, MN location in the Electrophysiology Medical Device division. In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. We are seeking a Manufacturing. Engineer I. This position will design and develop manufacturing processes and support production and service activities in order to meet daily production schedules while enhancing productivity, cost and product quality. Product lines supported are comprised of electronic systems used in our medical devices to better the lives of patients around the globe. | 12/18/2023 |
| 3517 | Abeona Therapeutics Cleveland, OH Manufacturing Associate MS in scientific discipline. Exp: 1-2 years |
Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. | 12/20/2023 |
| 3518 | Abeona Therapeutics Cleveland, OH Manufacturing Associate MS in scientific discipline. Exp: 1-2 years |
Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. | 12/20/2023 |
| 3519 | Analytical Biological Services Wilmington, DE Biorepository Technologist I (In-Sourced) Associate’s Degree in a medical or biological science is required. Bachelor’s Degree preferred. Exp: 1+ years |
Primary duties and responsibilities of the Biorepository Technologist I (In-Sourced) included but are not limited to: -Receive biospecimens including frozen, fixed, or fresh solid and liquid samples -Coordinate with shipping and receiving department to ensure all shipments are appropriately tracked -Coordinate with internal clinical study team to ensure sample and data accuracy -Communicates by written and verbal methods with related departments to assure samples arrive in the appropriate lab -Record sample quality concerns and provide feedback to collection site or central lab -Document sample information in laboratory database from source documents -Accession samples and appropriate data in the laboratories electronic data management system -Pull samples from inventory when requested by scientists for internal projects -Report and reconcile study data for management teams across departments -Provide Data management with scheduled monthly inventory reports and inventory reports upon Data managers request in a timely manner. -Upload monthly inventory reports to LIMS Labmatrix. -Organize and audit existing inventory QC and QC of sample location and data integrity -Ensure compliance with best practice guidelines, laboratory and EHS protocols, company standards and policies, standard operating procedures (SOP), and industry regulations. -Other duties as assigned | 12/20/2023 |
| 3520 | Analytical Biological Services Wilmington, DE Cell Culture Scientist BS or BA or higher degree in biological sciences. Exp: 1+ years |
- The position involves maintenance of cell culture lines to include thawing, expanding, harvesting and freezing lines. - Strict quality control guidelines of all products coming from cell culture must be monitored and adhered to. - Proper and aseptic maintenance of cell culture and production laboratory is required. - The Scientist must be able to effectively communicate with team members and clients of our progress with products and services and be able to respond quickly and accurately to client inquiries and requests. - Record keeping, excellent organizational skills and the ability to multitask are a must. | 12/20/2023 |
| 3521 | Absorption Systems Baltimore, MD Research Assistant undergraduate with a Life Sciences degree. Exp: entry-level |
We are seeking Research Assistants to join our Baltimore, MD clinical team! As a Research Assistant, you will be responsible for a variety of clinical research activities, ensuring that established protocols are followed, maintaining study protocol integrity, monitoring participant's status and safety, and playing a significant role in the training of clinical staff. We are conveniently located on the University of Maryland BioPark campus and provide paid parking for all employees. We have 12-hour day shifts, night shifts, and weekend shifts available. If you're seeking an entry-level role in Research, please apply. | 12/20/2023 |
| 3522 | Abveris Portland, OR Manufacturing Associate Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. The Manufacturing Associate will perform basic reagent handling, chemistry and molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom DNA based intermediates and products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. | 12/20/2023 |
| 3523 | Abveris Portland, OR Manufacturing Associate - Gene Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate, Gene Production, will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. The Manufacturing Associate will perform basic reagent handling, chemistry and molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom DNA based intermediates and products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. | 12/20/2023 |
| 3524 | Abveris South San Francisco, CA Manufacturing Associate, NGS TE Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate, NGS TE will perform basic molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture of variety of custom oligonucleotide products. The ideal candidate will be able to work independently, be very neat and organized, have the ability to follow established SOPs and complete manufacturing batch records to contribute to the daily production schedule. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. They will uphold standards as defined by the manufacturing process, work on continuous improvement and have good time management resulting in efficiency, and work in a safe manner. | 12/20/2023 |
| 3525 | Abveris Portland, OR Manufacturing Associate - Reagent Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. Shift: Tuesday-Saturday (3:00pm-11:30pm PST) The Manufacturing Associate will perform basic reagent handling, chemistry and molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom DNA based intermediates and products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. | 12/20/2023 |
| 3526 | Abveris South San Francisco, CA Associate Engineer Bioinformatics, Biopharma Libraries BS or MS in Computer Science, Bioinformatics, or related scientific/engineering field. Exp: 0 - 1 years |
Twist Biopharma is seeking an Associate Bioinformatics Engineer to develop and integrate workflows, analyses, and computational tools involved in the production and research of antibodies and proteins. While you have a broad interest in biotech and related scientific technologies, you also understand that computer science resources must be utilized to reach the scale required for our most complex solutions. The ideal candidate has computational/software/bioinformatics experience, and a basic knowledge of biology, DNA, antibody development, or protein sciences. He or she is comfortable with Python and JavaScript and will assist in the development of cutting-edge machine-learning applications, databases, and reports using modern tools, software development techniques, and coding best practices. | 12/20/2023 |
| 3527 | Abveris South San Francisco, CA Research Associate II, Process Development Research Associate: BA. Research Associate II: MSc. Exp: RA: 0-2 years; RAII: 0-2 years. |
The Research Associate II will interface between R&D and Operations to establish new processes at scale for DNA-based products in manufacturing. You will develop and support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput probe generation through robust experimental design. The ideal candidate will be driven and will do what it takes to keep manufacturing on track and constantly improving in a fast-paced startup environment. | 12/20/2023 |
| 3528 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst I B.S. degree in a relevant scientific discipline. Exp: 0-2+ years |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 12/20/2023 |
| 3529 | Adaptimmune Therapeutics Philadelphia, PA Quality Analytical Science and Technology Associate Scientist Bachelor’s degree in molecular biology, biomedical sciences or related specialties. Exp: 1+ years |
The purpose of this role is primarily to perform scientific work to support the Quality Control and Analytical Science and Technology team of analytical method and assay validations of Adaptimmune’s T-cell platform analytics. An Associate Scientist is broadly expected to support the team with the following duties. | 12/22/2023 |
| 3530 | Adare Pharmaceuticals Philadelphia, PA Analytical QC Chemist I Bachelor’s degree in chemistry, Biology, biochemistry, or related scientific field. Exp: 0-2 years’ |
The Analytical Chemist II is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 12/22/2023 |
| 3531 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences. Exp: BS: 1-3 years; MS: 1 year. |
Responsibilities: • Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing | 12/22/2023 |
| 3532 | Aimmune Therapeutics Dublin, OH Chemistry Technician BS in Related Science. Exp: 0-5 years |
Position Summary: The Technician position may undertake performance and documentation of routine tasks related to sample processing and assays using written operating procedures, standard laboratory methods and/or basic laboratory techniques, functions and equipment. To conduct specific procedures and tests both within and outside of the laboratory requiring the use of applied knowledge and practical skills learned from on-the-job experience; modify or adapt techniques to fit special needs or problems; to calculate data from routine tests to final results and to evaluate such results for accuracy where expected findings are not precisely defined, but sufficient guidelines exist for reference; to assist with and occasionally perform specialized and non-routine tests and assays, and to maintain records of such work; to coordinate and plan assigned work with other technicians and scientists. This position requires the following schedule pattern: Tuesday - Saturday 7:00am - 3:30pm OR Thursday - Monday 7:00am – 3:30pm | 12/22/2023 |
| 3533 | Aimmune Therapeutics Leonia, NJ Chemist B.S. in chemistry preferred. Exp: 1+ years |
Position Summary: The Chemist position is responsible for performing routine laboratory procedures in a quality control laboratory. Duties are performed under general supervision. Must be familiar with basic laboratory equipment and techniques. Responsibilities are focused on less complex testing and support functions. | 12/22/2023 |
| 3534 | Aimmune Therapeutics Dublin, OH Quality Technician undergraduate degree in closely related science preferred (i.e. Microbiology, Chemistry, Biology, et al.) Exp: 1 year |
Position Summary: This position performs and documents routine tasks related to sample processing and assays using written operating procedures, standard laboratory methods, and/or basic laboratory techniques, functions and equipment. The position conducts specific procedures and tests within the laboratory requiring the use of applied knowledge and practical skills learned from on-the-job experience; modify or adapt techniques to fit special needs or problems; to calculate data from routine tests to final results and to evaluate such results for accuracy where expected findings are not precisely defined, but sufficient guidelines exist for reference; to assist with and occasionally perform specialized and non-routine tests and assays, and to maintain records of such work; to coordinate and plan assigned work with other technicians and scientists. | 12/22/2023 |
| 3535 | Aimmune Therapeutics Bayport, NY Associate Technical Services Scientist/Specialist (TAG - Bayport, NY) Bachelor’s degree in Science, Chemistry, Chemical Engineering or in a related field required. Exp: 1+ years |
The Associate Technical Services Scientist/Specialist works within our Technical Applications Group (TAG) and will assist in formulating nutritional supplement products in various forms in support of manufacturing by collecting, evaluating, analyzing and summarizing data, address manufacturing issues, evaluate new technologies and/or ingredients and seek cost savings. Adherence to Standard Operating Procedures (SOP’s) and current Good Manufacturing Practices (cGMP’s) in this role is required. This position will work onsite Monday through Friday at Nestle Health Science’s manufacturing site in Bayport, NY (Long Island area). | 12/22/2023 |
| 3536 | Aimmune Therapeutics Mechanicsburg, PA Controls Technical Specialist I | $2,000 Sign On Bonus Eligible Associate’s Degree in a technical discipline Exp: 1+ years |
At Nestlé Purina PetCare, we’re a “safety first” culture, driven by a zero accident, zero defect, zero waste mentality. As a Controls Technical Specialist I, you’ll be responsible for troubleshooting, maintaining and enhancing the accuracy, reliability and system control’s data credibility of PLC and PC-based automation systems. In this role, you will oversee PLC upgrades and wiring modifications on production equipment and work directly with our maintenance team to troubleshoot and support production line modifications. As a Controls Technical Specialist I at our Mechanicsburg facility, you will enjoy competitive pay, $2,000 sign-on and retention bonus, premium pay, up to 5% quarterly bonus, $500 Lifestyle Spending each year, full health benefits, 401k match, generous PTO, excellent maternity/paternity leave and so much more! | 12/22/2023 |
| 3537 | Aimmune Therapeutics Flagstaff, AZ Associate Staff Engineer Bachelor’s Degree in Engineering or related field. Exp: 1+ year |
As an Associate Engineer, you will support the development of factory masterplans to align with Nestlé Purina long-term business objectives. You will have the opportunity to leverage your leadership skills while working with cross-functional teams at the corporate and factory levels. You will assist with delivering high value through technical scope development with supported justification, while adhering to project standards and strategies. Additionally, you will work on project submittal requirements and ensure quality while working closely with Nestlé Purina stakeholders. | 12/22/2023 |
| 3538 | Aimmune Therapeutics Solon, OH Product Development Associate BS or MS degree in Food Science, Food Engineering, Chemical Engineering, Packaging Science, Packaging Engineering, Mechanical Engineering, or related Exp: 0-3 years |
You will work hands-on the with our Pilot Plants and Factories, and Manufacturing facilities to deliver on the Innovation & Renovation (I&R) business objectives. You will dig into recipe (re)formulation, rapid pro-typing, and manage vendor relationships/interactions. You will help to build consumer insights and be the face of our products in cross-functional settings with commercial teams like Marketing, Sales, Finance. | 12/22/2023 |
| 3539 | Alkermes Wilmington, OH QC Analyst I Bachelor of Science degree in Chemistry or related scientific field. Exp: 1+ years |
The QC Analyst I performs testing of samples submitted to the laboratory in a cGMP compliant manner, as well as according to approved written procedures. The QC Analyst I may be required to write or revise SOPs, analytical procedures, or other analytical documentation at the discretion of quality control supervisory staff. | 12/22/2023 |
| 3540 | Alkermes Wilmington, OH Temp-QC Analyst-Microbiology Wilmington, OH, United States Bachelor's in science, preferably in Biology / Microbiology / Biotechnology or Biochemistry, required. Exp: 1+ year |
QC Analyst I must have broad knowledge of microbiology techniques within the laboratory required for the routine support of the microbiology laboratory operations. In this role the Analyst will be a fully functional member of the team responsible for testing and data entry for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment | 12/22/2023 |
| 3541 | Alkermes Wilmington, OH QC Analyst I/II Bachelors Degree in Chemistry. Exp: 0-2 years |
The position requires the individual to perform routine/non-routine physical, chemical, and in-vitro assays of clinical, commercial, process and cleaning validation samples, and process development samples to support Manufacturing. Performs physical and/or chemical analyses of product to ensure stability. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. | 12/22/2023 |
| 3542 | Alkermes Wilmington, OH Temp-Manufacturing Associate-Bulk-2nd Shift Associates degree or higher in a science/technical discipline. Exp: 0-1 year |
Perform all necessary operation activities in bulk manufacturing. These activities include but are not limited to the following: Equipment Cleaning, Equipment Set-up, Equipment/Automation Operation, and Batch Processing. Reads and follows detailed written SOPs / Procedures and detailed documentation of operations according to cGMP. Performs sample collection, equipment/process monitoring, and minor maintenance. Maintain individual training proficiency through individual Learning Management System. Other responsibilities include SOP writing and review of cGMP documentation. | 12/22/2023 |
| 3543 | Alkermes Wilmington, OH Manufacturing Associate-Bulk 2nd Shift Associates degree or higher in a science/technical discipline. Exp: 1+ year |
Perform all necessary operation activities in bulk manufacturing. These activities include but are not limited to the following: Equipment Cleaning, Equipment Set-up, Equipment/Automation Operation, and Batch Processing. Reads and follows detailed written SOPs / Procedures and detailed documentation of operations according to cGMP. Performs sample collection, equipment/process monitoring, and minor maintenance. Maintain individual training proficiency through individual Learning Management System. Other responsibilities include SOP writing and review of cGMP documentation. | 12/22/2023 |
| 3544 | Alkermes Wilmington, OH Process Engineer I/II/Lead-Filling Process Engineer I: BS degree in Engineering or technical discipline. Exp: 0-2 years |
Support and assist in the manufacture of pharmaceutical products for commercial and clinical supplies. Scale-up and transfer formulations/processes to production facility, design and recommend equipment purchases, write and execute qualification/validation protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process/equipment improvements (utilizing Change Control system) to reduce waste and increase process reliability. Support of manufacturing management in periodic review of existing and new revisions to manufacturing documentation in regard to, but not limited to, Operability, Technical accuracy (technical reviews), Compliance, Process Robustness. Perform process and equipment evaluation (FMEA, etc) to identify risks and weaknesses in new and current processes, Write or revise SOPs and other GMP documentation in support of new or changed manufacturing processes in cooperation with appropriate manufacturing personnel, Assure the resolution of deviations, corrective actions, action items from Change Control systems, and any audit non-compliance items. Develop and implement SOPs in support of new and upgraded processes, Develop and implement effective training of manufacturing personnel related to technical transfer and process upgrades, represent manufacturing on process design teams, Champion projects as they move into and through the manufacturing areas, Provide regular updates to manufacturing management on the status and issues involved in projects. | 12/22/2023 |
| 3545 | Alliance Pharma Malvern, PA Associate Scientist I- Immunoassay BA/BS or higher. Exp: 1-2 years |
• Prepare reagents, standards, and control samples • Analyze samples using various techniques specific to department • Perform method validation or qualification • Operate analytical equipment • Maintain analytical equipment • Ensure lab area is clean and inspection ready at all times • Remove lab waste • Record tasks in accordance with Good Documentation Practices (GDP) • Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11 • Follow applicable SOPs and procedural documents • Review and evaluate data results | 12/22/2023 |
| 3546 | Alliance Pharma Malvern, PA Assistant Scientist II BA/BS or higher. Exp: 1-2 years |
Prepare reagents, standards, and control samples · Analyze samples using various techniques specific to department · Operate analytical equipment · Maintain analytical equipment · Ensure lab area is clean and inspection ready at all times · Remove lab waste · Record tasks in accordance with Good Documentation Practices (GDP) · Learn and apply regulatory requirements; GLP, GCP, 21CFR Part 11 · Follow applicable SOPs and procedural documents · Learn how to review and evaluate data results · Other tasks as assigned | 12/22/2023 |
| 3547 | Prominex San Diego , CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 12/12/2023 |
| 3548 | RayzeBio Indianapolis, IN Microbiologist BS/MS in Biology, Microbiology, or other Life Science related field. Exp: up to five years |
Reporting to the Asst. Manager of Microbiology, the Microbiologist will help support the establishment of a new Environmental Monitoring/Microbiology laboratory which supports RayzeBio’s Radiopharmaceutical manufacturing facility in Indianapolis. The Microbiologist will be providing support for the commissioning, qualification, and validation of cleanroom environments and equipment and the associated environmental monitoring program. Upon establishment of the laboratory and program, the position will support the environmental monitoring and microbiological release testing of manufactured radiopharmaceuticals to support RayzeBio’s clinical and commercial programs. | 12/13/2023 |
| 3549 | RayzeBio Indianapolis, IN Radiopharmaceuticals Production Operator (I/II) Associate’s or Bachelor’s Degree in a STEM field is preferred. Exp: 1 – 4 years’ |
The Radiopharmaceuticals Production Operator will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As the Production Operator, you will play an active role in daily operations, striving to ensure each batch is right the first time and that the production area is kept in order at our manufacturing site in Indianapolis IN. You will be responsible for the production of RayzeBio drug products, strictly complying with good manufacturing practice and aseptic requirements. Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. As RayzeBio expands the production site and its portfolio of new products, you will support validation work for future company initiatives, and support management with internal projects and new hire training. The Radiopharmaceuticals Production Operator will report directly to the Production Manager. Operator level will be evaluated with experience and qualifications. | 12/13/2023 |
| 3550 | RayzeBio Indianapolis, IN Quality Control Chemist BS/MS in Chemistry, Science, or relevant field. Exp: up to five years |
Reporting to the Sr. Manager of Quality Control, the Quality Control Chemist will help support the establishment of a new Quality Control laboratory which supports RayzeBio’s Radiopharmaceutical manufacturing facility in Indianapolis. The Quality Control Chemist will be responsible and/or providing support for the installation, commissioning, qualification, and validation of analytical and radiochemical equipment for the QC lab. Upon establishment of the laboratory and program, this position will utilize a wide range of analytical and radiochemical analyses to support the advancement and release of novel targeted radiopharmaceuticals from the R&D phase through clinical development to GMP commercial radiopharmaceutical production. Specifically, the quality control chemist will support the release of manufactured radiopharmaceuticals to support RayzeBio’s clinical and commercial programs. | 12/13/2023 |
| 3551 | MacroGenics Rockville, MD Research Associate II Master’s degree in a scientific discipline. Exp: 0+ years |
The Research Associate II / Associate Scientist I position will support preclinical development of MacroGenics antibody-drug conjugates (ADC) through cell line engineering and molecular biology support. This position will independently develop and engineer cell lines, and conduct cell-based, molecular, and biochemical assays which contribute to the ADC research and development pipeline. | 12/13/2023 |
| 3552 | MacroGenics Rockville, MD Animal Health Technician I Bachelor’s degree in scientific discipline. Exp: 0+ years |
The Animal Health Technician I is responsible for executing animal care duties and responsibilities that enable us to support rapid advancement of preclinical programs. | 12/13/2023 |
| 3553 | Rockland Immunochemicals Pottstown, PA Associate Scientist/Scientist I, Molecular Biology Bachelor’s degree in biological sciences, biochemistry, or a closely related scientific field. Exp: 1-2 years |
Responsibilities include: RNA and DNA amplification and digestion (for transfection or transformation) as well as immunofluorescence assays, antibody validation (SDS, WB, Analytical SEC) Purification and characterization of recombinant protein targets using AKTA, ion exchange, affinity and size exclusion chromatography. Perform laboratory experiments independently or with other team members, including immunoassays, column production, affinity chromatography, and product handling Bacterial and mammalian expression of recombinant proteins, protein characterization including but not limited to: SDS page, western blot, dot blot, ELISA, Immunofluorescence Candidate is expected to perform basic mammalian cell culture Maintain laboratory space, equipment, and inventory in an appropriate and professional manner Lab housekeeping and solutions and materials restocking. Present data and final report suitable to deliver to clients Perform other duties as assigned | 12/13/2023 |
| 3554 | Rockland Immunochemicals Pottstown, PA Associate Scientist, Quality Control Bachelor’s degree in biochemistry, pharmacology, molecular biology, cancer biology, or related field or associate degree in similar field. Exp: 1+ years |
Rockland Immunochemicals is a worldwide leader in the development and commercialization of antibodies and antibody based tools. To further enable innovative biomarker development for drug discovery and diagnostic applications, we also offer highly customized solutions to meet basic, applied and clinical research demands. We are seeking a talented and highly motivated team player as an addition to our Quality Control Department. Join the group and apply your experience in the QC environment. | 12/13/2023 |
| 3555 | Toxikon Madison, WI Research Lab Analyst Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Analyst on our BioAnalytical team in Madison, WI. The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time. | 12/15/2023 |
| 3556 | Toxikon Greenfield, IN Research Assistant I - Cell Based and Immunology Team BS/BA degree in science or related field. Exp: 1+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 12/15/2023 |
| 3557 | Toxikon Greenfield, IN Research & Development Scientist Minimum of Bachelors in an appropriate scientific field. Exp: 1+ years |
Scientific Knowledge and Technical Expertise: Technical expertise in one or more of the following scientific disciplines is desired: Cell Culture and Cell-Based Potency Assays ELISA Statistics/Biostatistical experience pertaining to biopotency assays and/or In Vivo Relative Potency Assays. Virology qPCR Flow Cytometry Additional experience in Western blotting, Capillary IsoElectric Focusing, Capillary Electrophoresis, UV Spectroscopy and HPLC/ UHPLC is a plus. | 12/15/2023 |
| 3558 | Toxikon Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field. Exp: 1+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 12/15/2023 |
| 3559 | Toxikon Greenfield, IN Research Assistant I-Protein Chemistry BS/BA degree in science or related field. Exp: 1+ years |
In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 12/15/2023 |
| 3560 | Toxikon Research Triangle Park, NC Cytogenetics Technologist - 2nd Shift Bachelor's degree in Biology, Chemistry, Medical Technology or a related science. Exp: 1+ years |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Cytogenetics Technologist in RTP, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". Integrated Oncology, a LabCorp Specialty Testing Group, provides reference anatomic pathology, hematopathology and molecular pathology testing services to hospitals, health systems and independent oncology practices. Integrated Oncology is focused on providing world class solutions to better the lives of patients living with cancer. The schedule for this position will be 2nd Shift (Tuesday-Saturday 1pm-9:30pm) | 12/15/2023 |
| 3561 | Toxikon Greenfield, IN Laboratory Scientist Mammalian Cell Culture BA/BS in biology, molecular biology, microbiology, immunology, or a related field. Exp: 1+ years |
As a Laboratory Scientist, you will analyze samples for various compounds and components, run assays, perform mammalian cell culture, flow cytometry and perform data analysis and QC data in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. | 12/15/2023 |
| 3562 | Trevigen Minneapolis, MN Advanced Research Associate, QC Bioassay Master’s degree om the biological sciences or equivalent. Exp: 0 to 2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires experience with ELISAs, PCR, Western Blotting, and cell culture, including maintenance of cell lines and isolation of primary cells for use in the bioassays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 12/15/2023 |
| 3563 | Trevigen Minneapolis, MN Research Associate, Molecular Biology Master’s degree in Molecular Biology or equivalent. Exp: 0-2 years |
The responsibilities of this position are to assist the protein product development team in the area of recombinant protein expression. This includes the preparation of eukaryotic expression vectors, cell culture, and screening procedures. The successful candidate will perform various techniques such as DNA preps, sub-cloning, mammalian and insect cell culture, transfections, Western blotting, ELISA, and flow cytometry. They will also prepare buffers and reagents, assist in cleaning and maintenance of the laboratory and equipment, and perform other general lab duties as assigned. | 12/15/2023 |
| 3564 | Trevigen Minneapolis, MN Research Associate Bachelor’s degree in Biology, Biotechnology, Biochemistry or equivalent required. Exp: 0 to 2 years |
In this position you will build custom made-to-order kits for our rapidly growing Luminex product line, including qualification of assay components, formulation of intermediates, and preparation for packaging. | 12/15/2023 |
| 3565 | Trevigen Waltham, MA Medical Laboratory Technologist Bachelor of Science Degree in a chemical, physical or biological science. Exp: six months |
This position is responsible for performing high-complexity CLIA testing in day-to-day operations of the laboratory. | 12/15/2023 |
| 3566 | Trevigen Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0-2 years |
The responsibilities of this position are to prepare conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel. Perform additional duties as assigned. | 12/15/2023 |
| 3567 | Trevigen Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of stem cell and gene therapy medias. Perform QC testing and analysis of some cell culture media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Skills used include cell culture, high attention to detail, strong communication and organizational skills. This will be a Tuesday through Saturday work schedule. | 12/15/2023 |
| 3568 | Trevigen Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
We are seeking an Advanced Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 12/15/2023 |
| 3569 | Tyber Medical Bethlehem, PA Quality Engineer /Senior Quality Engineer Bachelor’s degree from a four-year college or university in a related field of study. Exp: one year |
The Quality Technician organizes and runs the routine analysis of the Quality Control Department. This job is essential in ensuring the Quality Control Department meets its goals of efficiency and customer satisfaction. This individual is responsible for conducting inspection and testing procedures during manufacturing processes and receiving inspection processes to ensure the products comply with requirements. | 12/15/2023 |
| 3570 | Universal Cells Seattle, WA Research Associate II, Gene Editing MS degree. Exp: 0-2 years |
The primary purpose of the Research Associate II position is to assist with gene editing of pluripotent stem cells. This position will work primarily in a laboratory setting in collaboration with other Scientists and Research Associates. | 12/15/2023 |
| 3571 | Vala Sciences San Diego , CA Research Associate (RA)/Senior Research Associate (SRA) – Assay Development and iPSC Maintenance B.S. or M.S. in Molecular/Cell Biology, Biochemistry, Neuroscience, Bioengineering, or related. Exp: 1+ years |
We’re seeking an RA or SRA to join our dynamic assay development and induced pluripotent stem cell (iPSC) research team. The successful candidate will execute validated assays for contract research projects and assist in management and maintenance of iPSC lines. Additionally, you will work with senior scientists in the Neurobiology and Cardiology groups to plan and perform experiments for assay development to support Vala’s internal and contract research projects. You will maintain differentiated iPSC cell cultures for live cell assays using Vala’s Kinetic Image Cytometry (KIC) technology, as well as perform IF staining to assist in development of reproducible and optimized assays. You may perform differentiation of iPSC to different cell types, such as neurons, astrocytes, microglia and cardiomyocytes. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 12/15/2023 |
| 3572 | Vala Sciences San Diego , CA Research Associate (RA)/Senior Research Associate (SRA) – iPSC Manufacturing B.S. or M.S. in Cell/Molecular Biology, Biochemistry, Neuroscience, or related field. Exp: 1-2 years |
The successful candidate will manage iPSC lines and their differentiation to different cell types, like cardiomyocytes, microglia, neurons, and astrocytes. These differentiated iPSC lines will be used for internal R&D projects, commercial research contracts, and manufacture for sale. You will evaluate and validate differentiated cell lines with biomarker detection methods like ICC or flow cytometry, and investigate and characterize cellular function using Vala’s live-cell fluorescent imaging technology. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 12/15/2023 |
| 3573 | VaxCyte San Carlos, CA Associate Scientist II, Upstream Development for Protein Development and Manufacturing MS in Biology, Chemical Engineering or Chemistry/ Biochemistry. Exp: 0-2+ years |
Vaxcyte is seeking a talented and energetic Associate Scientist I/II, to join the Upstream Process Development group within the Protein Development and CMC team. Vaxcyte is developing a multi-valent conjugate vaccine, based on a novel carrier protein produced using the XpressCFTM platform. This is an exciting opportunity to join a team aiming to establish a new fermentation development lab and pilot plant at Vaxcyte. | 12/15/2023 |
| 3574 | Vector Laboratories Newark, CA Technical Application Scientist II Master’s degree in Biology, Chemistry or related life science field required. Exp: 1+ years |
The Technical Support Scientist’s primary responsibility will be to provide product and application expertise, insight and troubleshooting assistance for all Vector Laboratories’ reagents to researchers across the life sciences fields and to our distributors worldwide. Also, as a member of the commercial team, the Technical Support Specialist will help in the generation of technical material and marketing content to support promotional activities and campaigns, as well as represent the company at conferences, meetings and vendor shows as required. The successful candidate will be self-motivated, a creative thinker and a problem solver who enjoys direct interaction with people. Candidate will be a team player with strong communication, organizational, and time management skills. Previous experience in a technical support role in a life science company would be beneficial. This position reports to the Sr Director, Commercial Operations. The ideal candidate for this position will be a collaborative problem solver, working to find the best possible solution to the client’s questions and needs. The candidate should embrace opportunities to learn more about our existing and upcoming products, as well as what our competitors are releasing. This is a collaborative, team, environment. To apply for this position, please email your resume and cover letter to: talent@vectorlabs.com. | 12/15/2023 |
| 3575 | VGXI Conroe, TX UPSTREAM MANUFACTURING PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: one to three Years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for upstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Upstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 12/15/2023 |
| 3576 | VGXI Conroe, TX DOWNSTREAM MANUFACTURING PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: one to three Years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for downstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Downstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 12/15/2023 |
| 3577 | VGXI Conroe, TX QUALITY CONTROL TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: one to three years |
The Quality Control Technician is responsible for in-process and release testing of products manufactured at VGXI. Responsibilities also include environmental monitoring of the production areas and raw material quarantine and release. Set-up, organization, and day-to-day operations of a Quality Control Lab are also required. | 12/15/2023 |
| 3578 | Viant Medical Brimfield, MA Quality Engineer Minimum of Associate’s Degree in Engineering or related technical field, with Bachelor’s Degree preferred. Exp: 0-3 years |
The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance. | 12/15/2023 |
| 3579 | Vividion Therapeutics San Diego , CA Research Associate I/II, Proteomics B.S. in Chemistry- or Biology-related field. Exp: 1-4 years |
Vividion Therapeutics is seeking a highly motivated Research Associate to help support the operation of our cutting-edge proteomics platforms. The successful candidate will have a high level of organization and attention to detail. The role will involve techniques such as cell culture, in vivo tissues processing, high throughput screening on an automated system, and protein chemistry or chemical biology. This position will help discover novel small-molecule ligands of protein targets through the execution of screens using our novel mass spectrometry-based proteomics platforms. | 12/15/2023 |
| 3580 | WaVe Life Sciences Cambridge, MA Research Associate II BS/MS in biology, biochemistry, cellular/molecular biology or related discipline. Exp: 1+ years |
Wave seeks a highly motivated biologist to join its research team in Cambridge, Massachusetts to support a rapidly expanding RNA-editing platform. This is an ideal position for an individual who is interested in working with cutting edge technologies and who thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate should have strong technical skills, and will be responsible for designing, executing, and analyzing experiments as a member of team focused on advancing therapeutic programs and discovery research platforms. | 12/15/2023 |
| 3581 | Frontage Exton, PA Associate Scientist/Scientist, BCGT Analytical Development Master's degree in, Molecular Biology, Cell Biology, or a related field. Exp: 1-2 years |
We seek a highly skilled Associate Scientist/Scientist to join our dynamic Molecular and Cell Biology team. This role will focus on developing analytical methods supporting biologics, cell, and gene therapy modalities. The ideal candidate will possess a deep understanding of tissue culture, cell line maintenance, cell-based assays, and proficiency in molecular approaches such as DNA/RNA extraction and PCR techniques. | 12/15/2023 |
| 3582 | Frontage Exton, PA Associate Scientist Bachelor’s or master’s degree in molecular biology, cell biology, biochemistry, or a related field. Exp: 1+ years |
The Cell-based Assay Core Lab, based at our Exton headquarters, stands as a premier provider of diverse cell-based assays. These include potency assays, neutralizing antibodies assays, EliSpot, virus plaque assay, TCID50 Assays etc. We are seeking a candidate with a fundamental understanding of Cell Biology, Biochemistry, and Molecular Biology. The ideal candidate should be highly organized, self-motivated, enthusiastic about learning, and capable of managing multiple projects concurrently. | 12/15/2023 |
| 3583 | Frontage Exton, PA Associate Scientist/Scientist – Protein Biochemist BS Degree or MS Degree. Exp: 1 year |
This is a bench scientific position for a competent and hardworking scientist with experience in protein purification and/or labeling of protein reagents. The person will be responsible labeling of reagents (protein and antibodies), purification and characterization including concentration estimation, SDS-PAGE, SE-HPLC, endotoxin estimations etc. He/she will be responsible for the quality of final product, record keeping and interacting with end user. The position will require excellent communication skills, and basic computer skills. | 12/15/2023 |
| 3584 | Frontage Concord, OH Laboratory Research Technician – Full time /Concord Ohio Educational Requirements: High School/GED or above (AS & BA/BS). Exp: entry-level |
Individuals in this position support evaluation of the safety and/or toxicity of pharmaceutical and biotechnology products by ensuring the health and welfare of research animals. | 12/15/2023 |
| 3585 | Frontage Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields. Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 12/15/2023 |
| 3586 | Frontage Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree. Exp: BS: 1+ years; MS: 0-3 years. |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 12/15/2023 |
| 3587 | PCI Pharma Services Bedford, NH QA Associate I - Operations Bachelor’s Degree in a relevant scientific discipline preferred. Exp: 0-2 years |
The Quality Associate I - Operations is responsible to provide QA support real-time for GMP Manufacturing of drug product. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products. | 12/4/2023 |
| 3588 | PCI Pharma Services Philadelphia, PA Process Engineer I Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout | 12/4/2023 |
| 3589 | PCI Pharma Services Philadelphia, PA Process Engineer I-2nd Shift Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout.**This is a second shift position. Hours are: 4pm to 12 Midnight, Monday to Friday** | 12/4/2023 |
| 3590 | PCI Pharma Services Philadelphia, PA Process Engineer I-Wkends AM Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout***This is a weekend position 6am to 6pm Friday, Saturday, and Sunday.** | 12/4/2023 |
| 3591 | PCI Pharma Services Rockford, IL Package Testing Engineer Bachelors degree in engineering and/or related discipline. Exp: 0-2 years |
The Package Testing Engineer supports PCI’s mission to provide industry-leading experience to clients, developing and commercializing solutions to optimize the delivery of lifesaving medicines and support better health outcomes for patients around the world. Reporting to the Principal Package Testing Lead, a successful Package Testing Engineer would utilize engineering skills and technical insights to evaluate, develop, test, and qualify effective packaging systems for PCI’s clients. Under the guidance of the Principal Associate, utilizing practical packaging development knowledge, effective report writing, and hands-on assembly skills, the Package Testing Engineer would support PCI’s Package Testing Services, commercial sales efforts as well as the successful commercialization of awarded packaging projects. In addition to the primary role of package testing, the incumbent would support package design and on-site prototyping projects as needed. Package Testing Engineer would support the workflows and reliability of the on-site Package Testing Lab and regularly coordinate projects with external partners. The Package Testing Engineer may engage clients, consultants, vendors, and suppliers directly to aid in the successful design and implementation of new packaging systems and products. | 12/4/2023 |
| 3592 | PCI Pharma Services Rockford, IL Serialization Engineer Bachelor's Degree in a related field. Exp: 1-5 years |
Serve as primary technical expert and principal designer/developer for all global major packaging line serialization design and integration efforts. Work closely with suppliers and internal colleagues to identify and specify complex line connectivity requirements and translate to comprehensive interface solutions specifications and delivery. | 12/4/2023 |
| 3593 | PharPoint Research Durham or Wilmington, NC Quality Assurance Auditor Bachelor’s degree (B.A./B.S.) or equivalent in a scientific, computer, or related discipline. Exp: 1-2 years’ |
Performs project and non-project quality assurance duties at PharPoint Research. Responsible for carrying out quality initiatives at the company, including but not limited to SOPs and training, computer systems validation, and Quality Management System. | 12/4/2023 |
| 3594 | PolyPeptide Group Torrance, CA Production Chemist I BS in Chemistry, Biochemistry, Biology or related science field. Exp: 1+ years |
Production Chemist is responsible for completing tasks & assignments in accordance with established processes & methodologies; synthesize peptides, intermediates, & processing from initial stage. | 12/4/2023 |
| 3595 | Poseida Therapeutics San Diego, CA Quality Control Analyst Bachelor’s degree in Life Sciences or related discipline. Exp: 1+ years |
Poseida Therapeutics, Inc. is seeking an outstanding candidate to join our Quality Control team. The Quality Control Analyst I will be a member of a dynamic team that ensures the safety of our products at various points during the manufacturing process by performing environmental monitoring, raw material and final product testing. As well as working cross-functionally with individuals and departments within the Pilot Plant Facility. | 12/4/2023 |
| 3596 | Kriya Therapeutics Morrisville, NC GMP Facilities Engineer Bachelor's degree in Engineering or related field. Exp: 1-3 years |
The GMP Facilities Engineer will be responsible for overseeing the facility's alarm response, deviation, change control, and CAPA management, ensuring compliance with Good Manufacturing Practices (GMP) in a biotech manufacturing environment. This individual will also play a crucial role in managing the Computerized Maintenance Management System (CMMS) and participation in project teams by serving as the representative of the facilities group. | 11/27/2023 |
| 3597 | Krystal Biotech Pittsburgh, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences. Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 11/27/2023 |
| 3598 | Krystal Biotech Pittsburgh, PA Manufacturing / Bioprocess Support Technician BS Degree in Biology, Engineering or related field is preferred. Exp: Entry Level |
Krystal Biotech, Inc is seeking a highly motivated Bioprocess Support Technician to support the growing Manufacturing team in Pittsburgh, PA. This role will perform a wide range of duties to support manufacturing processes in a GMP environment. | 11/27/2023 |
| 3599 | LakePharma
LakePharma
LakePharma
Camarillo, CA Microbiologist I Bachelor’s degree in Microbiology, Science or related field. Exp: 0-3 years |
Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Quality Control Microbiologist I performs quality activities in support of product production and releases. The position performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. | 11/28/2023 |
| 3600 | LakePharma
LakePharma
LakePharma
Lebanon, NJ Analytical Chemist I Bachelor’s degree in Chemistry or Chemical engineering. Exp: 1-2 year |
MAJOR DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Perform routine testing related to compendial monographs and general chapters; Saponification/Hydroxyl/Acid/Iodine Value, IR/UV analysis, Assays GC/HPLC analysis, ICP-MS analysis, Atomic Absorption spectrometry, etc. Perform measurements, computations, tabulation, and analyze results related to the testing conducted. Under the supervision of more experienced analysts, perform basic non-routine instrumental analysis and wet chemistry analysis in response to customer inquiries and projects as required. This may include but not limited to developing methods and performing method validation and verifications. Operate and maintain/calibrate laboratory equipment as per manufacturer’s recommendations and company’s Preventive Maintenance program. Maintain laboratory records related to all testing activities assuring that they are accurate and up to date. Perform other related duties as assigned. Perform all analysis and lab related duties as per cGMP. | 11/28/2023 |
| 3601 | Liquidia Morrisville, NC Manufacturing Technician B.S. degree. Exp: 0-2 year’s |
We are looking for a hands-on and experienced Manufacturing Technician. In this role, you will perform routine running of manufacturing equipment to support production and R&D efforts. Furthermore, you will provide feedback to engineering and scientific staff on process performance and ideas for process improvement. | 11/29/2023 |
| 3602 | Lygos Berkeley, CA Process Engineer B.S. in Chemical Engineer, Bioengineering, or related Engineering discipline. Exp: 1-2 years |
We are seeking a motivated Process Engineer to join our growing organization. As a key member of the pilot fermentation facility at Lygos, you will report to the Director of Fermentation and work closely with another Process Engineer on the team to support day to day operations of our pilot scale fermentations. You will support the fermentation team in maintenance and repair of fermentation equipment and contribute to the development of automation tools for the team. | 11/29/2023 |
| 3603 | Lyra Therapeutics Watertown, MA MSAT Engineer I/II Bachelor’s Degree (Engineering Preferred). Exp: 1+ years |
Our team is growing, and we are currently recruiting a Manufacturing Sciences and Technology (MSAT) Engineer I/II to support pharmaceutical operations at the Waltham and Watertown, MA sites. The focus of this position is to ensure manufacturing equipment and processes are operating as intended to meet the requirements for drug product manufacturing. This position will play a key role in delivering results in a fast paced, highly collaborative, and dynamic environment. The position will assist in the startup of a combination drug-device product from new product launch through commercial production. This involves process development, commercial process validations, technology transfers, as well as being accountable for commercial production. | 11/29/2023 |
| 3604 | Masy Biosciences Charleston, SC Environmental Monitoring Technician - 2nd Shift Bachelor’s degree preferred. Exp: 0-2 years |
The Environmental Monitoring Technician I is accounable for results in a fast-paced environment. The Level I Technician follows applicable SOPs and cGMPs to perform environmental monitoring for the facility, and may also perform simple, routine basic interpretation of environmental monitoring (EM) results, typically under supervision. This position is also responsible for hazardous waste and sanitation/cleaning of the Microbiology laboratory. The position requires strong leadership behaviors of the Alcami core competencies and non-negotatiables, as well as the functional competencies of this profile | 11/29/2023 |
| 3605 | Masy Biosciences Charleston, SC Pharmaceutical Manufacturing Technician - 1st Shift Associate’s degree preferred. Exp: 1-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. | 11/29/2023 |
| 3606 | Masy Biosciences Morrisville, NC QC Data Review Specialist - Chemistry Master’s degree in Chemistry, Biology, or related field. Exp: 1+ years |
The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing various activities at range of complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and process inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance-oriented training as necessary. The QC Data Review Specialist assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. Business needs and deadlines will require employee to perform work duties outside of standard work hours on occasion. | 11/29/2023 |
| 3607 | Masy Biosciences Charleston, SC Pharmaceutical Manufacturing Technician - 2nd Shift Associate’s degree preferred. Exp: 1-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. | 11/29/2023 |
| 3608 | Masy Biosciences Charleston, SC Pharmaceutical Manufacturing Technician - 3rd Shift Associate’s degree preferred. Exp: 1-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. | 11/29/2023 |
| 3609 | Meridian Life Science Memphis, TN Lab Production Associate Bachelor’s or Master’s degree from an accredited institution with a relevant scientific discipline such as Chemistry, Biology, Biochemistry, Molecula Exp: 1+ years |
The Lab Production Associate position is responsible for performing assigned manufacturing and laboratory support activities according to company policies, SOPs, and quality regulations. The position will be responsible for performing upstream and downstream bioprocessing procedures to support the commercial manufacturing of native antigens, recombinant proteins, antibodies, and blockers. Upstream processes include tissue culture, cell bioreactors, fermentation, virus propagation, cell and virus bank production, and buffer/media preparation. Downstream unit operations include harvest, clarification, chromatography, centrifugation, TFF (UF/DF), filtration, formulation, and fill-finish. The candidate will be required to maintain an assigned lab area and perform equipment and lab cleaning procedures. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO1345 regulations. | 11/30/2023 |
| 3610 | Meridian Life Science Memphis, TN Research Associate Bachelor’s degree from an accredited institution in a relevant scientific discipline such as Biology, Chemistry, Biochemistry, Molecular Biology etc. Exp: 1+ years |
The Research Associate will be responsible for providing hand-on support, within our Technical Operations and Development department, to drive the improvement and growth of our immunological reagent offerings including recombinant proteins, native antigens, antibodies, blockers, and custom manufacturing. The candidate will be expected to perform routine laboratory duties following company SOPs, protocols, and regulations. The role will assist with the execution of experiments under direct supervision of their supervisor performing experimental procedures, analytical procedures, analyzing data, and generating analysis reports. The candidate will be responsible for performing routine laboratory maintenance and lab management duties including maintaining sufficient supply of reagents, cleaning and disinfecting of laboratory equipment, cleaning lab area, environmental monitoring, and filling out proper paperwork. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO13485 regulations. The Research Associate will be responsible for providing hand-on support, within our Technical Operations and Development department, to drive the improvement and growth of our immunological reagent offerings including recombinant proteins, native antigens, antibodies, blockers, and custom manufacturing. The candidate will be expected to perform routine laboratory duties following company SOPs, protocols, and regulations. The role will assist with the execution of experiments under direct supervision of their supervisor performing experimental procedures, analytical procedures, analyzing data, and generating analysis reports. The candidate will be responsible for performing routine laboratory maintenance and lab management duties including maintaining sufficient supply of reagents, cleaning and disinfecting of laboratory equipment, cleaning lab area, environmental monitoring, and filling out proper paperwork. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO13485 regulations. | 11/30/2023 |
| 3611 | Myriad Genetics San Diego, CA Lab Tech II BS in Molecular Biology or related discipline. Exp: 1-2 years |
Execute high throughput preparations and dispenses of simple and complex reagents (enzyme formulations, primer combinations, large volume solutions) for our clinical lab using a variety of automated dispensing platforms; Assist in the receiving, handling, and monitoring of quantities and testing quality of raw materials and finished products; Assist in document manufacturing activities and quality control results; Auditing, stocking and equipment maintenance tasks | 11/30/2023 |
| 3612 | NAMSA Northwood, OH Microbiology Technologist Bachelor degree. Exp: no experience |
• May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. • Accurately collects and records raw data in logbooks and on worksheets. • May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. • May be required to perform required specific testing as applicable. • May be required to operate specified laboratory equipment. • May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable). • Other duties as assigned | 11/30/2023 |
| 3613 | NAMSA Northwood, OH LC-MS Chemist Master’s degree in chemistry or a related scientific field. Exp: no experience |
• Operates and maintains a variety of chromatographic and spectroscopic systems such as LC, LC/MS/MS, and GCMS to analyze biological and chemical elements as directed by assays or study protocols. • May order and/or stock supplies subject to approval. Maintain ancillary records (logbooks, worksheets). • Conduct routine studies independently according to work instructions. May be requested to conduct more involved studies. Routes all excursions or unusual testing occurrences to management. • Participate in the improvement of documents, test systems, quality systems, and workflow. | 11/30/2023 |
| 3614 | NAMSA Minneapolis, MN Laboratory Technician– Talent Pool An Associate or Bachelor degree in related scientific field is required. Exp: 1+ years |
• Conducts sample preparation for Sponsor materials as directed by study protocols for in vivo and in vitro biocompatibility assays and pharmacology, toxicology and analytical studies. • Performs the extraction process on prepared samples in accordance to ISO, USP and JMHLW regulations as directed by study protocols for biocompatibility assays. • Receives and logs Sponsor materials for testing. Completes chain of custody documentation for test article tracking. • Prepares and maintains sterile glassware for the sample preparation process. Processes glassware through washer, autoclave and depyrogenation oven as needed. • Operates, cleans and maintains incubators, autoclaves, hoods and other equipment routinely utilized. • Maintains an efficient and clean work area by organizing and restocking the sample preparation lab as needed. | 11/30/2023 |
| 3615 | NantKwest Culver City, CA Associate, Quality Control Bachelor’s degree in a life sciences discipline. Exp: 1+ years |
The Quality Control Associate in the Quality Control department is responsible for ensuring the timely execution of Quality Control Analytical assays in support of product release across all of ImmunityBio’s oncology and vaccine product platforms. This position will train on and perform a variety of molecular biology, and/or chemistry assays including but not limited to cell culture, ELISA, qPCR, HPLC, icIEF, CE-SDS techniques and/or Compendial test methods in the evaluation of product quality. | 11/30/2023 |
| 3616 | Nexelis Valencia, CA Laboratory Assistant Bachelor's degree in science preferred. Exp: 1+ years |
Process samples as required by each protocol. Assist laboratory technologists with sorting, processing, storage, and retrieval of medical specimens. | 12/1/2023 |
| 3617 | Nexelis Ithaca, NY Associate Scientist, LCMS (Sign on Bonus Offered) Bachelor’s Degree, Chemistry and/or Biology preferred. Exp: 1 year’s |
The Scientist Core LC/MS (Liquid Chromatography/Mass Spectrometry) employs liquid chromatographic separation techniques and mass spectrometric analysis for data collection. In addition to instrument operation, the Scientist LC/MS is responsible for some associated instrument maintenance, documentation in accordance with SOPs and regulations, and data processing in a manner which meets company quality best practices, objectives, and timelines. | 12/1/2023 |
| 3618 | Nexelis Ithaca, NY Associate Scientist Sample Preparation (Sign on bonus offered) Bachelor's Degree required. Exp: 1+ years |
Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments, and the preparation of solutions and reagents. | 12/1/2023 |
| 3619 | Nexelis Ithaca, NY Associate Scientist Sample Preparation (Sign on bonus offered) Bachelor's Degree required. Exp: 1+ years |
Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments, and the preparation of solutions and reagents. | 12/1/2023 |
| 3620 | Nexelis Indianapolis, IN Laboratory Assistant Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required. Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 12/1/2023 |
| 3621 | Nexelis Ithaca, NY Associate Scientist, LCMS (Sign on Bonus Offered) Bachelor’s Degree, Chemistry and/or Biology preferred. Exp: 1 year’s |
The Scientist Core LC/MS (Liquid Chromatography/Mass Spectrometry) employs liquid chromatographic separation techniques and mass spectrometric analysis for data collection. In addition to instrument operation, the Scientist LC/MS is responsible for some associated instrument maintenance, documentation in accordance with SOPs and regulations, and data processing in a manner which meets company quality best practices, objectives, and timelines. | 12/1/2023 |
| 3622 | Nexelis Austin, TX Laboratory Associate Associate degree Required or equivalent. Exp: 0–1-year |
Perform routine packaging and filling procedures with accuracy, consistency, and timeliness. Provide routine documentation and review of work performed in a timely manner. | 12/1/2023 |
| 3623 | Noble Life Sciences Sykesville, MD Research Technician Bachelor’s degree in biological sciences, biomedical engineering, or a related field. Exp: 1 year |
Description 1. Compliance: Perform assigned tasks and responsibilities under the direction of the Scientist(s) and/or the Study Director(s) and in accordance with relevant study protocols, regulations, and Standard Operating Procedures (SOPs). 2. Training: Ensure personal training is documented according to Noble SOPs prior to the performance of associated procedures. 3. Procedure Preparation: Label tubes and other supplies needed for collecting and processing specimens. Prepare reagents needed for collection or processing of specimens. 4. Performance of Procedures: Process various blood and tissue samples. Maintain quality, safety, and/or infection control standards. Perform procedures using various instrumentation according to Noble SOPs. 5. Documentation: Maintain lab notebooks and document experimental procedures and associated data. Assist in writing deviations and preparing responses to quality assurance audits related to duties performed. 6. Laboratory Maintenance: Take ownership of assigned laboratories. Coordinate with the inventory manager to stock assigned labs as needed. Maintain inventories of assigned cold storage units. Maintain the laboratories in a clean and organized manner. Prepare shipment packages as directed. 7. Collaborate: Collaborate with and assist other research technicians, research associates, study directors, study coordinators, and scientists across various departments. 8. Any other relevant duties as assigned. | 12/1/2023 |
| 3624 | Noble Life Sciences Sykesville, MD Jr. Research Associate Bachelor’s degree in biological sciences, biomedical engineering, or a related field. Exp: 1 year |
Ensure all necessary supplies needed to conduct the associated projects as specified by the protocols and/or SOPs are stocked. Print labels and label sample collection tubes and other laboratory reagents. Prepare data forms required to conduct the project as specified by the protocol and/or SOP. Assist in processing various blood and tissue samples. Assist in the preparation of samples using a variety of laboratory procedures for testing with various laboratory equipment. Conduct various laboratory procedures and operate analytical equipment. Maintain quality, safety, and/or infection control standards. Maintain the laboratories in a clean and organized manner after completion of procedures. Maintain lab notebooks and document experimental procedures and associated data. | 12/1/2023 |
| 3625 | Oakwood Labs Solon, OH Quality Control Chemist- Pharmaceuticals Bachelor's degree in Chemistry, Biochemistry, Biology, or related field. Exp: One to four years' |
We are adding to our Quality Control Chemistry Staff. We are currently seeking individuals to: Perform analytical testing of raw material, in-process product, final product release and stability testing. Clear documentation of test activities in approved worksheets and laboratory notebooks. Execute mathematical calculations as outlined in test methods. Assess data to determine if the material tested meets specifications. Peer review of quality control data. Participate in investigational testing and assist with root cause analysis. Create and review SOP’s and author Change Controls. Other general lab related duties as necessary | 12/1/2023 |
| 3626 | Oakwood Labs Oakwood Villiage, OH Chemist Bachelor’s degree in chemistry, biology, or related discipline. Exp: entry level |
Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development | 12/1/2023 |
| 3627 | Pacific BioLabs Hercules, CA Microbiology Laboratory Analyst I/II An undergraduate or AA degree in a science-related field (e.g., Microbiology, Biological Sciences). Exp: 0-3+ years |
PBL has immediate openings for full or part time Microbiology Laboratory Analysts in the Microbiology Services Department. The Microbiology Laboratory Analyst will report to Microbiology Management and will contribute to general laboratory testing, sample management, and laboratory maintenance. The Microbiology Laboratory Analyst is expected to participate with the team to meet Microbiology Services Department goals and perform routine laboratory duties as directed. | 12/1/2023 |
| 3628 | Pacific BioLabs San Francisco Bay Area, CA Quality Assurance Specialist I Associate or B.S. in Chemistry, Biology, Microbiology, or equivalent experience required. Exp: 0-2 years |
Pacific BioLabs has immediate openings for full time Quality Assurance Specialist I in the Quality Assurance Department. The QA Specialist I will report to the Chief Quality Officer or designated individual. The Quality Assurance Specialist I is responsible for assisting management with the maintenance of the Quality Systems. The QA Specialist I must be sensitive to the demanding regulatory compliance requirements attending to the operation of a pharmaceutical testing laboratory. This job also requires the ability to demonstrate a high commitment to interpersonal relations. Work must be performed in compliance with Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Quality System Regulations (QSR), ISO quality management system requirements, and other necessary regulatory requirements (e.g. OSHA, EPA, CDC, USDA, OLAW, etc.) as required by the task at hand, as well as any additional duties as assigned by the Chief Quality Officer. | 12/1/2023 |
| 3629 | Patheon Middleton, WI Entry Level Chemist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 12/1/2023 |
| 3630 | Patheon St. Louis, MO Scientist I, Electrophoresis Analytical Development Bachelor in Molecular Biology / Chemistry / Biochemistry / Chemical Engineering, or a related field. Exp: no experience |
Responsible for developing or transferring analytical methods to support biopharmaceutical process development. You will work within an interdisciplinary team of scientists where you will learn and supply your skills and ideas to projects. | 12/1/2023 |
| 3631 | Patheon Cincinnati, OH R&D/Mfg Scientist I Associate’s or Bachelor’s degree in physical science; Chemistry or Biology preferred. Exp: 1+ years |
As a Laboratory Team Member, you will coordinate with your supervisor and collaborate with colleagues in diverse groups to assure that critical timelines are met. You will have the opportunity to collaborate with your peers within the laboratory and those in other departments such as formulations, operations, project management and quality assurance on a regular basis. You will perform analytical methods for elaborate testing for validated and experimental methods and other tests as needed to support lab operations. You will participate in the validation of analytical test methods when additional resources are required. | 12/1/2023 |
| 3632 | Patheon Cincinnati, OH Scientist I, Formulation & Process Development Minimum Bachelor of Science (BS) in science/engineering related field. Exp: 1+ years |
Supports execution for the development of new formulations and manufacturing processes of solids, liquids, and semi-solid dosage forms. Increase and develop knowledge regarding drug toxicology, pre-clinical – phase III, scale-up, and registration. Connect with technical leads, supervisors and project team peers (analytical and project management) on the progress and timely completion of activities and critical milestones. | 12/1/2023 |
| 3633 | Patheon Burlington, MA Labs FSP Associate Scientist - Raw Materials GMP Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1 year |
This position will work with others in Quality Control, Analytical Development teams, Quality Assurance, Manufacturing and CROs to support routine QC testing for Raw Materials for the manufacturing of Gene therapy products. The Analyst will specifically support the Raw material and gene therapy program pipeline (as needed) including but not limited to Project Management of the raw material program and development of testing strategies. | 12/1/2023 |
| 3634 | Patheon Middleton, WI Associate Scientist (Sunday -Thursday or Tuesday - Saturday) Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 12/1/2023 |
| 3635 | Patheon Middleton, WI Associate Scientist - Mass Spec Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 12/1/2023 |
| 3636 | Charles River Laboratories Mattawan, MI Research Analyst I - Formulations 1 Bachelor’s/Master’s degree in a relevant field. Exp: no experience |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. The pay range for this position is $23.50/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. The shift is for the weekend, Friday to Monday 6 AM-2:30 PM but will train for the first 12 weeks Monday-Friday 6 AM-2:30 PM. When you work Saturday or Sunday there will be a 10% shift differential. | 11/20/2023 |
| 3637 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Tuesday through Saturday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 11/20/2023 |
| 3638 | Charles River Laboratories South San Francisco, CA Research Technician II - In Vitro B.S. or A.S. degree in a Life Science discipline, such as biology, veterinary science, or a related field. Exp: 1 - 2 years |
We are looking for a highly motivated Research Technician II - In Vitro (Rodent Facility) to join our Insourcing Solutions team located in South San Francisco, CA. | 11/20/2023 |
| 3639 | Charles River Laboratories Cleveland, OH Research Analyst I- Bioanalytical Bachelor’s degree (BA/BS). Exp: no experience |
We are seeking a Research Analyst I for our Bioanalytical Chemistry Team at our Safety Assessment site located in Cleveland, OH. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 11/20/2023 |
| 3640 | Charles River Laboratories Mattawan, MI Research Analyst I - Bioanalytical 1 Bachelor’s degree (BA/BS). Exp: no experience |
We are seeking an experienced Research Analyst for our Safety Assessment site located in Mattawan, MI. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP's and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 11/20/2023 |
| 3641 | Charles River Laboratories Mattawan, MI Analytics Associate I Bachelor’s degree (Mathematics, Statistics, or Computer Science preferred). Exp: 0-2 or more years |
SALARY: The hourly rate for this position is $27.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. SCHEDULE: Monday - Friday, 8:00am - 4:30pm *flexible start and end time after 1-3 months of training We are seeking an experienced Analytics Associate for our Biostatistics Team at our Mattawan, MI site. An Analytics Associate is responsible for producing custom tables with statistical analyses using established systems and / or standardized code, to be completed in an accurate and timely manner consistent with the direction provided by the study director. | 11/20/2023 |
| 3642 | Charles River Laboratories Durham, NC Research Technician I Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline. Exp: 1+ years |
We are seeking a Research Technician I for our Discovery site located Durham. The following are responsibilities related to the Research Technician I: • Perform routine research activities as assigned, including in vivo-based screens. • Perform dosing of laboratory animals, animal husbandry. • Prepare & verify dosing solutions for administration. • Ensure that all individual study supplies are on-site & prepared in a timely manner. • Perform equipment maintenance. • Review protocol with manager to insure proper study execution. • Prepare & organize study data, study folders & data forms; perform data collection and entry. • Review study report, gives feedback on the accuracy of the materials & methods section; report data to more senior staff. | 11/20/2023 |
| 3643 | Hemacare Mattawan, MI Research Technician - Pharmacokinetics & Acute Toxicology 1 1 Bachelor’s/Master’s degree. Exp: no experience |
We are seeking an experienced Research Technician for our Pharmacokinetics & Acute Toxicology Team located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 11/20/2023 |
| 3644 | Hemacare San Diego, CA Husbandry Technician I B.S. in either animal science or life sciences preferred. Exp: one (1) year |
We are looking for a Husbandry Technician I (Rodent Facility) to join our Insourcing Solutions team located in San Diego, CA. | 11/20/2023 |
| 3645 | Hemacare Cambridge, MA Animal Support Technician I B.S. in Animal Science, Biology, or Biological Science. Exp: 6+ months’ |
We are seeking an Animal Support Technician to join our Insourcing Solutions team, located in Cambridge, MA. | 11/20/2023 |
| 3646 | Integra LifeSciences Plainsboro, NJ Manufacturing Engineer Bachelor's degree in Engineering (Mechanical Engineering, Pharmaceutical Engineering, Chemical Engineering, Biomedical Engineering). Exp: 0-2 years |
The Manufacturing Engineer will play a key role in the support of manufacturing operations, process scale–up, and manufacturing improvement activities. They will oversee projects to evaluate, analyze, and improve existing processes, support the development of new manufacturing processes, implement statistical process controls, analyze and trend existing process parameters, improve manufacturing yields, reduce scrap, and error proof manufacturing processes. | 11/21/2023 |
| 3647 | Integra LifeSciences Boston, MA QC Analyst I, Analytical - 2nd Shift Bachelor’s Degree in the biological or chemical sciences or equivalent. Exp: 1-3 years’ |
The QC Analyst I, Analytical – 2nd Shift, will be responsible for performing quality control Analytical laboratory testing of in-process, finished goods, validation studies, and adherence to all applicable regulations, policies, and procedures purchased components, manufactured sub-assemblies and final product. Must have working knowledge of U.S. Food and Drug Administration regulations, ISO 13485, and other applicable regulatory agencies as they pertain to laboratory testing. | 11/21/2023 |
| 3648 | MEDTOX Burlington, NC Research Associate I, Lab Automation Bachelor’s degree in chemistry, computer science, or an equivalent scientific discipline. Exp: 1+ years |
The Research Associate I-Lab Automation will be part of the Research and Development team that supports automation efforts in robotic liquid handling and data analysis. In this role, you will use mass spectrometry and other analytical technologies, provide assay development and validation support and assist in training and orientation of personnel as assigned. | 11/22/2023 |
| 3649 | MEDTOX Greenfield, IN Research Assistant I - Cell Based and Immunology Team BS/BA degree in science or related field. Exp: 1+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/22/2023 |
| 3650 | MEDTOX Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field. Exp: 1+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 11/22/2023 |
| 3651 | MEDTOX Greenfield, IN Research Assistant I-Protein Chemistry BS/BA degree in science or related field. Exp: 1+ years |
We have an excellent opportunity for someone to join our Protein Chemistry team in Greenfield, IN. In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/22/2023 |
| 3652 | MEDTOX Indianapolis, IN Analyst - BioAnalytical Lab, 2nd shift Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. Schedule: This is a 2nd shift position (2:00pm-10:30pm) scheduled Monday through Friday | 11/22/2023 |
| 3653 | MEDTOX Madison, WI Analyst Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Precipitation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time. | 11/22/2023 |
| 3654 | MEDTOX Madison, WI Research Lab Analyst Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time. | 11/22/2023 |
| 3655 | Merck West Point , PA B63 Associate Specialist, Engineering Bachelor’s Degree in Science or Engineering. Exp: 1+ years |
The Polysaccharide Vaccine (PV) Technical Operations team is seeking a highly motivated individual to fill an open position to support the start-up, process qualification, and successful licensure of new bulk vaccine manufacturing facility, Building 63, at West Point. The Associate Specialist, PV Technical Operations is responsible for technical support for bulk vaccine manufacturing unit operations while actively supporting, participating in, and embracing an empowered team culture. In this role, the Associate Specialist will work as an individual contributor as well as a team member within a cross-functional group that includes West Point Operations, Quality, Automation, Deviation Management, Global Technical Operations, Research and Development Division, and others. | 11/22/2023 |
| 3656 | Merck Elkton, VA Associate Manufacturing Science & Engineering Specialist Bachelor degree or higher in engineering, science, or business fields. New graduates or anticipated Fall 2023 graduates are also encouraged to apply. Exp: entry level |
At our Company's campus in Elkton, Virginia, we have an entry level position available to support and sustain our manufacturing processes. The manufacturing facility is located in the Shenandoah Valley along the Shenandoah River and the Blue Ridge Mountains a short distance from the University of Virginia and James Madison University. The successful candidate will have the opportunity to apply their enthusiasm and technical skills as a member of a multidisciplinary team supporting the operation of pharmaceutical, biopharmaceutical, and vaccine product manufacturing facilities. Depending on interests, education, experience, and skills, successful candidates will be matched with positions across the Elkton campus and may have the opportunity to participate in developmental rotations across functional areas. | 11/22/2023 |
| 3657 | Merck West Point , PA Off-Shift Specialist, Engineering Bachelor’s Degree in Science or Engineering. Exp: 1-3 years |
We are seeking a highly motivated individual to fill an open off-shift position to support the start-up, process qualification, and successful licensure of new bulk vaccine manufacturing facility, Building 63, at West Point. The Specialist, Operations is responsible for technical support for bulk vaccine manufacturing unit operations while actively supporting, participating in, and embracing an empowered team culture. In this role, the Specialist will work as an individual contributor as well as a team member within a cross-functional group that includes West Point Operations, Quality, Automation, Deviation Management, Global Technical Operations, MRL, and others. | 11/22/2023 |
| 3658 | Merck Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey. The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 11/22/2023 |
| 3659 | Merck Kenilworth and Rahway, NJ Associate Scientist, Biologics Process Research & Development BS (or expected completion by May 2024) in Chemical/Biochemical/Biomedical Engineering, Biotechnology, Biochemistry, Microbiology, Structural biology, Exp: 1+ years |
In April 2020, our Company announced plans to consolidate our New Jersey campuses into a single New Jersey headquarters location in Rahway, NJ in 2023 and 2024. Therefore, this role will be temporarily based in Kenilworth and exact timing of the departmental move to Rahway, NJ will be communicated at a future date. Our Research Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we partner to deliver the next medical breakthrough. Biologics Process Research & Development (BPR&D) within our company's Research Laboratories in our Research Division is on a mission to rapidly deliver diverse biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies. To achieve this, we work closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical, Formulation, and Commercial Manufacturing while providing a diverse and inclusive environment for all. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies. Examples include investments for development of continuous manufacturing, green and sustainable processes, and proprietary technology platforms. We actively publish and engage with the scientific community to influence the field. BPR&D includes three lab-facing technical functional areas: Process Cell Sciences (PCS), Upstream Process Development (UPD) and Downstream Process Development & Engineering (DPDE). This job posting covers opportunities for all three functional areas. We are actively looking for highly motivated people with a passion for innovation and interest in contributing to one or more of the three technical functional areas mentioned above. As an Associate Scientist in BPR&D you will work with a highly collaborative team of scientists and engineers to design, develop and execute robust processes in support of early- to late-stage biological products. You will apply rigorous scientific principles to solve challenging problems focused on developing the best processes to deliver life-changing medicines to patients worldwide. You will also have an opportunity to contribute to additional areas of interest such as biophysical, process, economic and/or multivariate modeling as we are committed to leveraging digital ways of working to enhance our ability to design robust processes. | 11/23/2023 |
| 3660 | PerkinElmer Annapolis, MD Chemical Media Buffer Technician Associate Degree in a chemistry, biology, or other relevant discipline. Exp: 1+ years |
Responsibilities: Perform FACS (Fluorescence-activated cell sorting) machine QC daily. Tasks include but are not limited to emptying sheath waste, refilling sheath tank and running daily test cycle. Perform preventative maintenance on the DNA sequencing machines. Task is performed 3 times weekly. Tasks include emptying and refilling buffer trays, rinsing and drying critical parts and contacting respective end-users with any issues or material orders. Check ViCell reagents and cups in all locations twice a week. Track levels of remaining ViCell reagents and cups and inform Lab Consumable Supplies when more needs to be ordered. Check volumes and fill Multitron and Stability chamber carboys 3x per week. (Mobile phase solutions for HPLC). Distribute distilled water for incubators daily. Deliver RODI (reverse osmosis deionized) and USP water to designated Labs. Distribute FBS from central stock to appropriate locations once per week; monitor central stock and track usage to inform when the reordering process needs to occur. | 11/24/2023 |
| 3661 | Sanofi Waltham, MA mRNA Senior Research Associate - Vaccine Bachelors in a related field (e.g., Cell Biology, molecular biology, biochemistry, etc.). Exp: 1-3 years |
As a part of the Discovery biology group at Sanofi's mRNA Center of Excellence (CoE), our team leads the development and implementation of high-throughput screening techniques to aid in the development of our next generation mRNA vaccines. Our team functions transversally and as such gets to work alongside all of the other R&D groups to achieve our goal of advancing our mRNA platform to the next generation. | 11/24/2023 |
| 3662 | Sanofi Framingham, MA Research Associate, Gene Therapy - Genomic Medicine Bioanalytics BS in biological sciences or related field. Exp: 1 – 3 years |
The Sanofi Genetic Medicine Unit CMC organization is responsible for the design and optimization of gene and cell therapy manufacturing processes and platforms. A key function of this group is to establish operational excellence in the manufacturing of Sanofi’s emerging portfolio of gene therapy products. The bioanalytical group provides analytical testing to support in process, release, and stability testing, as well as development activities for process optimization and life cycle management from early to late-stage clinical entry. The Research Associate is responsible for executing test methods under control of established procedures. Additional functions will include interpretation of data, preparation of test documentation, and management of analytical databases. We are looking for a candidate that is capable of learning quickly with the goal of executing analytical methods and managing assigned test schedules, with excellent communication skills. The position is primarily located in Framingham, MA but will be moving to Waltham, MA in Q4, 2022 | 11/24/2023 |
| 3663 | Sanofi Waltham, MA Senior Research Associate, Genomic Medicine Unit - Cell Culture Process Development Master’s degree in biological science or engineering discipline. Exp: 1+ years |
The Genomic Medicine Unit (GMU) CMC group at Sanofi is dedicated to the establishment of best in class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV vectors, lentiviral vectors and cell therapy products. This organization encompasses vector and cell line engineering, upstream and downstream process development, analytics, and clinical manufacturing support. The cell culture process development group is responsible for viral vector production optimization and development of next generation production platforms to support high dose therapeutic products. The group is seeking a motivated Senior Research Associate to join the team | 11/24/2023 |
| 3664 | Sanofi Framingham, MA Senior Research Associate - QC, Genomic Medicine Bioanalytics - CT Master’s degree in Biology/Biochemistry or related discipline. Exp: 1+ years |
This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi’s CMC Development organization. The GMU Analytical Development group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust analytical methods to support release and characterization testing of different cell therapy candidates. The group supports cGMP-compliant in-process Quality Control (QC) support of cGMP Manufacturing cutting edge methods such as flow cytometry. The selected candidate will execute rapid turnaround cGMP testing of in-process materials. In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month | 11/24/2023 |
| 3665 | Sanofi Waltham, MA Senior Associate Scientist, Genome Engineering-NGS, Genomic Medicine Unit Master’s Degree. Exp: 1 year |
We are seeking a Sr. Associate Scientist to be part of a team focused on next generation sequencing in genome and cellular engineering in the Genomic Medicine Unit. The successful candidate will play a key supporting role in application of genome editing technology as an approach for treatment of cancer, rare blood and/or rare genetic diseases. | 11/24/2023 |
| 3666 | Sanofi Waltham, MA Senior Research Associate - Pilot Plant Operator Waltham, MassachusettsSenior Research Associate - Pilot Plant Operator Waltham, Massachusetts MS in a related discipline. Exp: 1+ years |
The gene therapy development and manufacturing group in Sanofi is responsible for the design and optimization of viral vector manufacturing processes and platforms. A key function of this group is to establish operational excellence in the manufacturing of gene therapy materials and products, through the development and implementation of robust and safe manufacturing practices, capable of supporting program needs, that are aligned with Sanofi internal standards and evolving regulatory expectations The manufacturing operations team is responsible for the safe and compliant execution of established manufacturing procedures to meet aggressive program deliverables. The team is responsible for “transfer-in” of manufacturing operations from development, as well as manufacturing of product to support internal program needs and external technology transfers for early and late-stage clinical gene therapy products. The Senior Research Associate will be responsible for executing upstream and operations under control of established manufacturing procedures and cross training of junior staff as needed. | 11/24/2023 |
| 3667 | Sanofi Framingham, MA Senior Manufacturing Technician Associate’s degree or Bachelor's degree. Exp: AS: 1-3 years; BS: 1-2 years |
This is a 12-hour, rotating position for within our Downstream Manufacturing team at our 8 NYA facility. 8 NYA is an integrated, continuous, biomanufacturing facility (ICBF). The facility is operated by Upstream, Downstream and Support Service groups which support a 24/7 large-scale therapeutic protein manufacturing facility housing multiple products. Initial job responsibilities will include supporting a diverse range of manufacturing related activities during plant start-up from Operational Commissioning/Shakedown through process validation (PV) and commercial operations. The Senior Manufacturing Technician will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 11/24/2023 |
| 3668 | Invitrogen St. Louis, MO Scientist II, Process Development Master’s degree or foreign degree equivalent in Chemistry, Biology, Biochemistry, Chemical Engineering, or a related field of study. Exp: 1+ years |
DUTIES: Works with a variety of chromatography techniques including reverse phase, size exclusion, affinity, and ion exchange chromatography. Assists with the design of experimental plans based on defined deliverables. Conducts semi-routine and moderately complex tasks and sample analysis to support process development. Functions as a process subject matter expert in a cGMP environment. Assists with preparing protocols, reports, and test methods. Maintains and ensures safe laboratory environment and work practices. Executes, records, and evaluates experimental data appropriately, including the writing and revising of process development reports and technology transfer protocols as needed. | 11/24/2023 |
| 3669 | Invitrogen St. Louis, MO Scientist I, Electrophoresis Analytical Development Bachelor in Molecular Biology / Chemistry / Biochemistry / Chemical Engineering, or a related field. Exp: no experience |
Responsible for developing or transferring analytical methods to support biopharmaceutical process development. You will work within an interdisciplinary team of scientists where you will learn and supply your skills and ideas to projects. | 11/24/2023 |
| 3670 | Invitrogen St. Louis, MO Biopharmaceutical Production Technician II Bachelor’s degree in Biology, Biochemistry or Chemistry (or related) Exp: 1+ year |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 11/24/2023 |
| 3671 | Invitrogen St. Louis, MO Formulation Technician I (Day Shift) Associates in a relevant scientific field or bachelor’s degree in Biology, Biochemistry or Chemistry preferred. Exp: AS: 1-3 years; BS: 0+ years |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. They will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. We're currently hiring Biopharmaceutical Technicians and Buffer & Media Technicians on Day and Night shifts (12/hour shifts either 6:00AM-6:30PM or 6:00PM-6:30AM on a rotating schedule of a 2/2/3). Minimum base pay is $21/hour (plus built-in overtime). Base pay can vary per education, experience and position level. | 11/24/2023 |
| 3672 | Invitrogen St. Louis, MO QC Scientist I Bachelor’s degree in STEM field preferred. Exp: no experience |
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. | 11/24/2023 |
| 3673 | Invitrogen St. Louis, MO QC Scientist I - Environmental Monitoring Bachelor’s degree in STEM field preferred. Exp: no experience |
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale! Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. | 11/24/2023 |
| 3674 | Invitrogen St. Louis, MO Scientist I, QC Microbiology (4x10 Days; Wed - Sat) Bachelor’s degree required in a scientific field, preferably a Microbiology or Biology. Exp: 0 - 2 years |
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. | 11/24/2023 |
| 3675 | Jordi labs Mansfield, MA Senior Chemist 1 - Must be local to Mansfield, MA Masters of Science in Chemistry Exp: 1+ years |
Job Summary: Candidate will be responsible for Reports Preparation; preparing technical reports summarizing findings related to mass spectroscopy (LCMS, GCMS, PYMS) and chromatography methods (HPLC, GC), Designing Analyses; designing and implementing analytical strategies to help resolve complex, real world analytical problems including material failures, deformulations and quantitation, Performing Analysis; direct or perform mass spectroscopy or chromatographic analyses including overseeing method development and performing existing methods, Discussing Results; skilled at discussing analytical data and would be able to communicate in simple terms the results from a series of analytical tests. This would include helping other team members with interpretation as well as discussing results with customers. | 11/24/2023 |
| 3676 | Stryker Portage, MI Entry-level Electrical Design Engineer, R&D Bachelor's degree in Electrical Engineering or related discipline. Exp: 0+ years |
At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development. | 11/13/2023 |
| 3677 | Acrotech Biopharma Dayton, NJ CHEMIST A BS/MS in a Scientific field. Exp: 1-3 years’ |
The Chemist will perform a variety of testing to assess the strength, identity and purity of finished product, which are mainly oral solids and/or raw materials. The Chemist will work as a member of a team to effectively plan and develop/validate new methods (for Assay, Dissolution, Residual solvents, and Related compounds tests) to execute analytical testing and/or test using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 11/14/2023 |
| 3678 | Acrotech Biopharma Durham, NC ASSISTANT SCIENTIST BA/BS in Chemistry, Pharmaceutical Sciences or related field. Exp: 0+ years |
Capable of performing test methods for complex formulations under general oversight and documenting those experiments per cGMP requirements. Must be able to calculate, organize, and communicate results via standard data templates and reports. Experience in a cGMP laboratory and testing inhaled product (e.g. MDI and DPI) samples is preferred. Must possess good organizational skills, a commitment to quality work, and good oral and written communication skills, and work effectively as part of a team. | 11/14/2023 |
| 3679 | Acrotech Biopharma Dayton, NJ CHEMIST A BS with Chemistry is one of the subjects would be preferable. Exp: 1-3 years |
Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 11/14/2023 |
| 3680 | Repligen Auburn, MA Applications Engineer I Bachelor’s degree in engineering. Exp: 1-2 years |
Responsibilities Working closely with commercial team, convert customer conceptual design into a product solution that meets customer applications need Guide customer in selection of various raw materials that aligns with business preferred raw material Generate finish product cost estimates Product setup in ERP system which includes but not limited to creating Item Master, manufacturing router and Bill of materials. Initiate / Approve Engineering Change Orders for raw materials and finished products Travel required <10 % of time to visit industry events and customer visit | 11/14/2023 |
| 3681 | Cel-Sci Baltimore & Elkridge, MD Validation Technician B.S. in science or engineering or a related discipline or 2-year degree. Exp: BS: 0+ years; AS: 1 to 2+ years |
The Validation Technician is responsible for supporting validation activities of GMP equipment and systems. Assists in specifying and selecting equipment. Maintains all records related to qualification and validation. Prepares validation reports, suggests, and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Technician reports to the Validation Engineer. | 11/14/2023 |
| 3682 | Cel-Sci Baltimore & Elkridge, MD Validation Engineer B.S. in a related discipline. Exp: 1 to 5+ year |
The Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor. | 11/14/2023 |
| 3683 | Cel-Sci Elkridge, MD Manufacturing Process Technician BS/BA Degree in a related field or AA Degree in a related field. Exp: BS: 0+ years; AS: 1+ years |
The Manufacturing Process Technician contributes to the manufacturing team and participates in the manufacture of LI under GMP, and in process development and facilities operations and maintenance. The Manufacturing Process Technician reports directly to Supervisor of Manufacturing. | 11/14/2023 |
| 3684 | Cogent Professionals Indianapolis, IN Cellular Biologist/Biochemist BS - Biology, Cell/Molecular Biology, Biochemistry or related field or MS. Exp: 1-3 years |
We currently have a role available for a Cellular Biologist/Biochemist with industrial pharma experience. Job duties include, but are not limited to: Developing methods and assays, running assays efficiently, and recording and interpreting data. Strong cell culture (pre-clinical/mammalian) and aseptic technique skills needed. Ability to present data and summarize conclusions in written and oral forms. Utilizing Western blots, gel electrophoresis, MS and other biochemistry/molecular biology techniques. | 11/14/2023 |
| 3685 | Cogent Professionals San Diego, CA Entry-level Pharma Chemist BS-Chemistry or related field. Exp: 0-2 years |
We currently have a role available for an Entry-level Pharma Chemist. Job duties include, but are not limited to: Receiving and managing routine and daily orders. Weighing and preparing samples for storage and shipping. Sharing best practices and improvement opportunities. Working with laboratory automation (i.e. Hamilton, Tecan, etc.). Clearly documenting all laboratory duties. Keeping lab space clean and safe. | 11/14/2023 |
| 3686 | Cogent Professionals Pasadena, CA Molecular Biologist/Biochemist BS-Biology, Molecular/Cell Biology, Biochemistry, or related field. Exp: < 1 year |
We currently have a role available for a Molecular Biologist/Biochemist. Job duties include, but are not limited to, the following: Cell culture on a moderate scale and plating 96-well plates. Prepare reagents for automated liquid handling system. Preliminary analysis of data to verify completeness and accuracy. Some biochemistry background would be highly desirable, including Western Blot. Knowledge of liquid handling robots would be a plus (Tecan). Thorough documentation of experimental procedures via eLN (Benchling), reports, and technical documents. Compliance with all electronic notebook, safety, and quality SOPs is a must. Willingness to prepare and communicate technical presentations as needed. | 11/14/2023 |
| 3687 | Cogent Professionals Pasadena, CA Synthetic Chemist BS-Chemistry, Organic Chemistry, or related field or MS. Exp: BS: 1-3 years; MS: 0-1 years |
We currently have roles available for skilled Synthetic Chemists with industrial pharma lab experience. Job duties include, but are not limited to, the following: Synthesis of small molecules and proficiency in synthetic organic chemistry. Understanding standard unit operations (e.g., reaction set up, work up, flash column purification, isolation, and characterization), along with demonstrated technical problem-solving ability, is a must. Synthesis of peptides using automated peptide synthesizers and solution chemistry. Purification using preparative RP-HPLC, flash chromatography, FPLC, SEC, or equivalent. Bioconjugation of peptides/proteins using standard techniques. Strong expertise running and interpreting NMR, HPLC, and LC-MS data. Thorough documentation of experimental procedures via eLN, reports, and technical documents. Compliance with all electronic notebook, safety, and quality SOPs is a must. Willingness to prepare and communicate technical presentations as needed. | 11/14/2023 |
| 3688 | Debut Biotechnology San Diego, CA Research Associate - Downstream Process Development Bachelors/Masters degree in Chemistry, Chemical Engineering, or related subject. Exp: 0-2 years |
Debut Biotechnology is seeking a Research Associate in downstream process development for small molecule purification. You will assist in the development of robust & scalable downstream processes, and support pilot-scale process operations to maximize product yield. This individual should have familiarity with phenomena that can be leveraged for purification on a molecular level, as well as those that can be applied for physical material separations. As such, those with backgrounds in chemistry & chemical engineering are strongly encouraged to apply. Research Associate II and Senior Research Associate level candidates will also be considered. The successful candidate will work closely with the internal members of the downstream process development team, as well as the cross-functionally with fermentation scientists, pilot plant associates, biologists, chemists, and engineers. | 11/15/2023 |
| 3689 | Dicerna Pharmaceuticals Clayton, NC Filling Technician I - AP - Days AAS degree in a related field preferred. Exp: one (1) year |
The Position Filling of insulin & media preparations under aseptic conditions & operation of inspection equipment in order to achieve production goals | 11/16/2023 |
| 3690 | Dicerna Pharmaceuticals Clayton, NC Manufacturing Process Technician I - FP - NIGHTS AAS degree or military training preferred. Exp: six (6) months |
The Position Operate Assembly/Packaging manufacturing equipment in order to achieve production goals. | 11/16/2023 |
| 3691 | Dicerna Pharmaceuticals West Lebanon , NH Manufacturing Technician Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. We offer both day and night shift positions (schedule below). With the growth of our site, we are seeking night shift suppport. Day Shift (7:00am-7:00pm) : Sun-Tuesday everyother Wedneday Thur-Saturday everyother Wednesday Night Shift (7:00pm-7:00am- includes 15% shift differential): Sunday-Tuesday everyother Saturday Wednesday-Friday everyother Saturday | 11/16/2023 |
| 3692 | Dicerna Pharmaceuticals West Lebanon , NH Manufacturing Technician - Night Shift Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. With the growth of our site, we are seeking night shift support. We offer the following shift schedules that include a 15% shift differential: 7:00pm-7:00am (everyother week has 8-hours built in overtime): Sunday-Tuesday and everyother Saturday Wednesday-Friday and everyother Saturday | 11/16/2023 |
| 3693 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Associate degree in a laborat Exp: 1-3 years |
Purpose of the Position: Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 11/17/2023 |
| 3694 | DxTerity Rancho Dominguez, CA Research Associate B.S. or M.S Degree in Biochemistry, Molecular Biology or a related field. Exp: 1-3 years |
DxTerity, a patient-centric genomics company located in Los Angeles, CA is looking to hire a Research Associate to join our Research and Product Development team. Responsibilities include: development of molecular diagnostic test kits, reagents and procedures in a team environment. Perform experiments independently after receiving general direction from supervisor. Make detailed observations, analyzes data and interpret results. Prepare technical reports, summaries, protocols and quantitative analyses. Maintain and develop skills in molecular biology and company technology through reading of internal reports and scientific literature. Support the achievement of project objectives and time schedules while meeting ISO and FDA regulatory and design control requirements. | 11/17/2023 |
| 3695 | Etubics Culver City, CA Associate, Quality Control Bachelor’s degree in a life sciences discipline. Exp: 1+ years |
The Quality Control Associate in the Quality Control department is responsible for ensuring the timely execution of Quality Control Analytical assays in support of product release across all of ImmunityBio’s oncology and vaccine product platforms. This position will train on and perform a variety of molecular biology, and/or chemistry assays including but not limited to cell culture, ELISA, qPCR, HPLC, icIEF, CE-SDS techniques and/or Compendial test methods in the evaluation of product quality. | 11/17/2023 |
| 3696 | Fluxergy Irvine, CA Manufacturing Engineer Bachelors or Masters degree in Mechanical Engineering or equivalent engineering degree. Exp: 1 to 3 years |
About the Role Are you a passionate and experienced Manufacturing Engineer ready to take on exciting challenges in the world of manufacturing and process engineering? Do you thrive in a dynamic, cross-functional environment where your skills can make a real impact? If so, we have the perfect opportunity for you! | 11/17/2023 |
| 3697 | Fluxergy Irvine, CA R&D Mechanical Engineer - Product Development Bachelor or master's in mechanical engineering, Biomedical Engineering, Bioengineering preferred. Exp: 1-4 years |
About the Role Would you enjoy taking the latest version of our flagship product from the design stage – all the way to a successful FDA 510K submittal - then commercialization? Does the idea of using your engineering skills to help decentralize traditional laboratory infrastructure sound like a cause you can get behind? If you answered ‘yes’ to both questions above, apply today! Your resume will be reviewed within days - everyone who applies will hear back from us. | 11/17/2023 |
| 3698 | Forbius Montreal, Quebec, CA Sample Manager and Biobank Coordinator Bachelor’s degree (B.Sc.) in Biochemistry, Cell Biology, Life Sciences or a related field. Exp: one (1) year |
We are currently looking for a multi-skilled Sample Manager and Biobank Coordinator to join our growing team in Montréal. In collaboration with our preclinical, translational and clinical teams, the incumbent will be in charge of sample management associated to our preclinical and clinical programs. | 11/17/2023 |
| 3699 | Free Think Technologies Branford, CT Analytical Scientist? Bachelor’s or master’s degree in chemistry, chemical engineering, or related scientific field. Exp: 0-6 years’ |
We are seeking a full-time Analytical Scientist to work in our laboratories in Branford, Connecticut. KEY RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO Perform analytical measurements including HPLC/UPLC, GC, KF and dissolution testing Ensure all work performed complies with company standard operating procedures Develop and maintain technical expertise through continuing professional education and training | 11/17/2023 |
| 3700 | Fujifilm Diosynth College Station, TX Quality Control Cell Biology Analyst I Undergraduate degree in Biology or science related field; OR AAS in biology or science related field.Undergraduate degree in Biology or science relate Exp: BS: 0+ years; AAS: 1 year |
Summary The Cell Biologist I, under general direction, will be responsible for performing routine and non-routine quantitative and qualitative analysis of samples submitted to the Quality Control (QC) Laboratory. | 11/17/2023 |
| 3701 | Fujifilm Diosynth College Station, TX Quality Control - Microbiology Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field. Exp: 0+ years |
Summary: The Microbiology Analyst I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. | 11/17/2023 |
| 3702 | Haemonetics Clinton, PA Manufacturing Engineer Automation I Bachelor's Degree Engineering Exp: 0-2+ years |
This position is responsible to develop and implement changes to product design and/or to the manufacturing process to achieve significant quality, or cost improvements. Requires participation in new product development and existing programs, working with other business units to identify design-for-manufacturability issues and ensuring these issues are addressed prior to release.in a timely manner. | 11/17/2023 |
| 3703 | Haemonetics Clinton, PA Manufacturing Engineer I Bachelor's Degree Engineering; Master's Degree Engineering. Exp: 0-3+ years |
This position is responsible to develop and implement changes to product design and/or to the automation and manufacturing process to achieve significant quality, or cost improvements. Requires participation in new product development programs, working with other business units to identify design-for-manufacturability issues, ensuring these issues are addressed prior to release, and mentoring engineers. | 11/17/2023 |
| 3704 | Pace Analytical Lenexa, KS Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3705 | Pace Analytical Mt. Juliet, TN Scientist 1 - RadChem Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3706 | Pace Analytical Mt. Juliet, TN Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3707 | Pace Analytical Mt. Juliet, TN Environmental Scientist - Entry Level Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: Entry Level |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3708 | Pace Analytical Lenexa, CA Scientist 1 - Chemistry, Biochemistry Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3709 | Pace Analytical Mt. Juliet, TN Chemist (Scientist 1) Shift Differential Offered! Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3710 | Pace Analytical Ormond Beach, FL Chemist (Scientist 1) Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3711 | InVivo Biosystems Eugene, OR Lab Technician I - Zebrafish Husbandry Associates or Bachelor degree in Biology or related field preferred. Exp: one year |
This is a collaborative, team-based role with the responsibility to support transgenic and phenotyping client and grant-funded projects. On any given day you may perform zebrafish husbandry, general laboratory upkeep for zebrafish and c. elegans research. As you will be joining a growing biotech company, a passion for science, a positive outlook, and an ability to work in a dynamic environment are a must. | 11/17/2023 |
| 3712 | Ionetix Lansing, MI Mechanical Engineer (Lansing, MI) Bachelor’s degree in mechanical engineering. Exp: 1+ years |
Ionetix Corporation is seeking a Mechanical Engineer to design, develop, prototype, test and release mechanical and electromechanical designs of cyclotrons, automated chemistry systems, and related products. | 11/17/2023 |
| 3713 | Ionetix Sarasota, FL Site Production Technician (Sarasota, FL) A degree in a science field such as chemistry, microbiology, pharmaceutical, medical technology. Exp: 1+ years |
Ionetix is seeking a full-time Site Production Technician in Sarasota, Florida. This position will operate the cyclotron and purification unit to manufacture and release PET products, fully integrating the tracer production at the point of imaging. | 11/17/2023 |
| 3714 | Vigene Biosciences Rockville, MD Quality Control Associate - Environmental Monitoring B.S in Biology or related field. Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Analyst I will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 11/17/2023 |
| 3715 | Boston Scientific Arden Hills, MN Quality Engineer I - Electrical Bachelor's degree or higher in Electrical Engineering. Exp: 1+ years |
The Electrophysiology (EP) Design Quality Assurance team is looking for an engineer to evaluate manufacturing and design changes. EP has a broad portfolio of capital equipment used in the field to support ablation and diagnostic procedures. The EP Design Quality assurance team is growing, and the timely evaluation of design changes is key to maintaining a robust EP Capital Equipment portfolio to reduce potential safety and quality issues. This role provides visibility across the Research and Design organization. The selected candidate will collaborate with Manufacturing, Product Complaints, Regulatory, and Field Servicing engineering. This is a significant role for an entry-level engineer with opportunities to grow into Computer Programming, Cybersecurity, Risk, or Electrical Design. The selected candidate will be mentored by a Senior Electrical Engineer. | 11/17/2023 |
| 3716 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to help confirm mailing addresses in our directory. Mostly Googling. Can do work any time, any place. Must be able to accept payment via PayPal or Venmo. If interested, send a message through the contact form. Thanks! | 11/6/2023 |
| 3717 | Covance Greenfield, IN Research Assistant I - Cell Based and Immunology Team BS/BA degree in science or related field. Exp: 1+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/6/2023 |
| 3718 | Covance Greenfield, IN Research Assistant I - Protein Chemistry BS/BA degree in science or related field. Exp: 1+ years |
If you have a passion for science and working in a dynamic and fast paced lab with a cohesive team, the Research Assistant position will take you to the next level in your career. We have an excellent opportunity for someone to join our Protein Chemistry team in Greenfield, IN. In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/6/2023 |
| 3719 | Covance Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field. Exp: 1+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 11/6/2023 |
| 3720 | Covance Indianapolis, IN Research Assistant I BS/BA degree in science or related field. Exp: 1+ years |
Analyzes biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. | 11/6/2023 |
| 3721 | Covance Indianapolis, IN Analyst - BioAnalytical Lab, 2nd shift Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. Schedule: This is a 2nd shift position (2:00pm-10:30pm) scheduled Monday through Friday. | 11/6/2023 |
| 3722 | Covance Indianapolis, IN Research Assistant II Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1-2 years |
As a Research Assistant II in Bioanalytical Services you will be part of a cohesive team and conduct routine analysis on biological and chemical samples in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines for multiple studies. | 11/6/2023 |
| 3723 | Dexcom Mesa, AZ Process Engineer I Bachelor’s degree in a technical discipline. Exp: 0-2 years |
In this role, you will use sound and proven engineering principles to assist in designing and developing processes and requirements. The projects and activities will focus on Dexcom’s sensor technology. Working as a member of a technology team, you will collaborate with other engineers, management, and operators. This position will lead efforts to prove out manufacturing and automation processes to achieve design requirements specified by R&D, and explore and evaluate new technologies and concepts through analysis, prototyping, fixture design, and experimentation. This position will transfer and scale up new products from R&D. Involvement may begin from feasibility at vendors to full scale manufacturing. | 11/7/2023 |
| 3724 | Exact Sciences Madison, WI Clinical Laboratory Scientist - Tuesday - Friday, 8:00pm - 6:30am Bachelor's degree in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution. Exp: 1+ years |
The Clinical Laboratory Scientist I performs laboratory analysis on clinical specimens using established laboratory procedures. The Clinical Laboratory Scientist I duties will include but are not limited to; processing of specimens, performance of moderate, and highly complex analytical testing, establishing, performing and documenting quality assurance, quality control, equipment maintenance, and accurately documenting all work performed under the direction of the Laboratory Medical Director. As a Clinical Laboratory Scientist I, you will recognize and resolve problems using good laboratory practices. Training: Monday - Friday, 7:00am - 3:30pm for the first 4 weeks Location: 650 Forward Drive and 145 E. Badger Road | 11/7/2023 |
| 3725 | ICON plc. San Antonio, TX Laboratory Assistant Bachelor’s degree (preferred). Exp: 1 year |
Duties: • Monitoring samples/Troubleshooting discrepancies. • Consolidating created samples/containers (i.e. slides, blocks, reports, etc.) • Searching and retrieving documents and samples. • Performing data entry/Monitoring e-mails and various correspondences. • Checking that slides/blocks are properly barcoded and labeled. • Assisting the pathologists with the technical/clerical work. | 11/7/2023 |
| 3726 | ICON plc. San Antonio, TX Laboratory Assistant Bachelor's degree (preferred). Exp: 1 year |
Duties: • Monitoring samples/Troubleshooting discrepancies. • Consolidating created samples/containers (i.e. slides, blocks, reports, etc.) • Searching and retrieving documents and samples. • Performing data entry/Monitoring e-mails and various correspondences. • Checking that slides/blocks are properly barcoded and labeled. • Assisting the pathologists with the technical/clerical work. | 11/7/2023 |
| 3727 | Eli Lilly Cambridge, MA Chemist/Sr Chemist - RNA Therapeutics BSc or MSc in Organic Chemistry or related field. Exp: 1+ years |
The successful candidate for this Chemist/Senior Chemist position will have a strong research track record in synthetic organic chemistry, be analytically minded, embrace data-driven decision making, and have experience in oligonucleotide chemistry and or bioconjugation. He/she will provide key technical knowledge and collaborate within a multidisciplinary team to support the development of next-generation RNA based therapeutics. | 11/8/2023 |
| 3728 | Eli Lilly Cambridge, MA Biologist - Cell Biologist Neurodegeneration BS and/or MS. Exp: 1+ Years |
The Cell Biologist position will be within the Proteostasis Group, which is part of the larger Neurodegeneration division. The primary responsibility will be culturing iPSC derived motor neurons as a cellular model of Amyotrophic Lateral Sclerosis to support the development of therapeutic agents. | 11/8/2023 |
| 3729 | Eli Lilly Cambridge, MA Biologist –Cell Biologist/Biochemist Neurodegeneration BS and/or MS. Exp: 1+ years |
The Cell Biologist/Biochemist position will be within the Proteostasis Group, which is part of the larger Neurodegeneration division. The primary responsibility of the role will be to develop and optimize cellular models of neurodegenerative disease as a platform for therapeutic development. The role will be focused on the biology of aggregate prone proteins such as TDP-43, synuclein or tau. | 11/8/2023 |
| 3730 | Eli Lilly Cambridge, MA Biologist –Biomarker Development Neurodegeneration BS and/or MS. Exp: 1+ years |
The Biomarker Development position will be within the Proteostasis Group, which is part of the larger Neurodegeneration division. In order to effectively diagnose and treat neurodegenerative diseases the identification and measurement of biomarkers is vital. The primary responsibility for this role will be the identification, development and optimization of assays which will support biomarker discovery for neurodegenerative disorders, such as ALS, Parkinson’s Disease and Alzheimer’s Disease. | 11/8/2023 |
| 3731 | Eli Lilly Indianapolis, IN Chemist- Nucleic Acid Synthesis Bachelor's and/or Master's degree. Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 11/8/2023 |
| 3732 | Eli Lilly Pasadena, CA Chemist / Biochemist Undergraduate degree in chemistry, biochemistry, chemical engineering. Exp: 0+ years |
The team at Protomer is working on responsive biotherapeutics that can be controlled using small molecule modulators. Protomer team is based in Pasadena and the research labs are located in Pasadena. We are currently expanding the team to advance several programs, including glucose sensing insulins (GSIs), and are looking for a research associate with experience in biochemistry, synthesis, bioconjugations, and purification/characterization of therapeutic compounds of interest. The ideal candidate will have a bachelor’s or master’s degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a team player in a fast-paced research setting. The applicant will be responsible for assisting Protomer’s senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively participate and present in team meetings and is expected to contribute to the team’s progress and success. | 11/8/2023 |
| 3733 | Eli Lilly Boston, MA Engineer, Downstream Process Development - Akouos M.S in Biochemistry, Chemical Engineering, Bioengineering or related discipline. Exp: 1+ years |
The Process Development group at Akouos is seeking an innovative Engineer to provide hands-on development support for the manufacturing of AAV-based gene therapy vectors. The ideal candidate for this position is an entry level Engineer with a background in AAV vector purification technologies and gene therapy downstream process development. The successful candidate will actively participate in downstream process development, scale-up, process optimization, and process tech transfer for GMP manufacturing. The successful candidate will thrive in a collaborative, scientifically stimulating, and fast-pace work environment. | 11/8/2023 |
| 3734 | Organogenesis Canton, MA Production Associate I-Collagen A Biotech certificate, Associate's degree, Bachelor's degree in Biology or a related science discipline is strongly preferred. Exp: 1+ years |
The Production Associate I - Collagen performs activities involved in the production of Collagen These activities include, but are not limited to, protein purifications, filtrations, and titrations in the production of high quality, purified, sterile collagen for both internal and external customers. This position requires working in a regulated area under the direct supervision of a team leader or departmental supervisor. | 11/8/2023 |
| 3735 | Organogenesis Canton, MA Production Associate I Bachelor’s degree or Biotech certificate. Exp: 1+ years |
The Production Associate will perform all activities involved in one of the following areas: the aseptic processing of a living product; the production of ICL and FortaFlex Products; or activities associated with HTP Product under the direct supervision the Manager. This role will support the Manufacturing Team by performing the tasks that will assure the safe and timely processing of our products, working in a Class 100/ISO 5, Class 10K/ ISO 7 and/or Class 100K/ISO 8 cleanroom. Sunday-Thursday schedule or Monday-Friday schedule, approximately 7:30am-4:00pm. Some weekend and holiday work required. | 11/8/2023 |
| 3736 | Meridian Medical Technologies Rocky Mount , NC MS&T Associate Process Engineer Bachelor’s degree. Exp: zero to one years |
As an Associate MS&T Engineer, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams. | 11/8/2023 |
| 3737 | Meridian Medical Technologies Rochester, MI Chemist / Microbiologist Master’s degree. Exp: 1+ years |
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to patients. Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology from R&D. As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. | 11/8/2023 |
| 3738 | Meridian Medical Technologies Andover, MA QC Technician (2nd Shift) Biotechnology Certificate/Associate Degree. Exp: 0-2 years |
You will be a member of Pfizer’s dedicated and highly effective Quality Control team. You will support commercial manufacturing and QC testing labs by managing sample lifecycle including bulk sample receipt, aliquot, labeling, delivery, and storage of QC test samples. Sample types may include release test, backups, retains, reference material, assay controls, and stability. You will support and maintain the retain program as required by CFR regulations. Monitoring of environmental chambers is also critical to the storage of the above sample types. Your contribution to the Quality Control Sample Operations team will help Pfizer provide safe drugs to patients. | 11/8/2023 |
| 3739 | Meridian Medical Technologies Rocky Mount , NC QC Chemistry Lab Analyst I Bachelor’s degree. Exp: 0+ years |
Your prior work experience and ability to apply your breadth of knowledge will help you adapt the standard methods and procedures. You will help us identify required delivery and process improvements that drive increased efficiency, throughput and quality. You will arrive at decisions on which methods and procedures are the best fit for different work situations. | 11/8/2023 |
| 3740 | Meridian Medical Technologies Rocky Mount , NC Manufacturing Quality Engineer- Quality Distribution Bachelor's Degree. Exp: 0 to 1 year |
You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing and packaging of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. | 11/8/2023 |
| 3741 | Meridian Medical Technologies Kalamazoo, MI QC Laboratory Analyst II (1st Shift) Bachelor’s degree in Chemistry, Biochemistry or related science. Exp: 0-1 years |
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. You will also be relied on for setting requirements for the transfer of methodology from R&D. You will be developing and applying your knowledge of procedures, techniques, tools, materials and equipment. Your receptiveness to new ideas will enhance the team’s ability to achieve goals and targets. You will follow standard procedures to complete tasks and identify process issues or problems that involve direct application of your skills/knowledge. | 11/8/2023 |
| 3742 | Meridian Medical Technologies Sanford, NC QC Senior Associate Scientist - Method Transfer and Validation BS/BA Degree in Science/related field. Exp: 0 years |
You will be a member of Pfizer’s dedicated and highly effective Quality Control Team at Sanford, NC. Key responsibilities in QC Method Transfer and Validation (MTV) are performing tasks/activities associated with analytical method qualification, validation, verification and transfer. Specific activities include authoring/executing/review of protocols and reports associated with analytical method qualification/validation/transfer to support Pfizer’s quality programs. You will be responsible for participating in method transfer/validation activities to support Demo, Engineering, CTM (Clinical Trial Material), product/process validation and commercial batches manufactured at Pfizer. Additional responsibilities will include driving continuous improvement/Operational Excellence/innovative implementations and represent QC MTV on cross functional teams. Key responsibilities in this role include executing method transfer activities (verification, co-validation, validation, qualification) in the QC laboratory. Other responsibilities may include testing support, SOP revision, LIMS review etc. | 11/8/2023 |
| 3743 | Regeneron Tarrytown, NY Process Development Associate II, Analytics BS Exp: 0 – 2 years |
Regeneron's Preclinical Manufacturing & Process Development (PMPD) Analytics group is seeking a laboratory Scientist or Engineer interested in the analytical characterization of biopharmaceuticals. In this role, you will conduct analytical experiments that support manufacturing process development and research activities in a fast-paced laboratory setting. | 11/09/2023 |
| 3744 | Regeneron Tarrytown, NY Process Development Associate II, Cell Culture Development (PMPD) BS or MS in Chemical Engineering or Bio-related Engineering Exp: 0-3 years |
The Cell Culture Development Group within Preclinical Manufacturing and Process Development (PMPD) is looking for a motivated person to work as part of the medium and feed development team on projects for mammalian cell culture process medium optimization. In this role, you will perform studies at small scale to develop cell culture medium that improves cell growth, cell productivity, and/or product quality to support the extensive Regeneron clinical pipeline. | 11/09/2023 |
| 3745 | Regeneron Tarrytown, NY Sample Management Associate BS degree Exp: 0-4 years |
Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Sample Management Associate to support biobanking operations and sample data processes. | 11/09/2023 |
| 3746 | Regeneron Tarrytown, NY Sample Management Associate BS degree Exp: 0-4 years |
Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Sample Management Associate to support biobanking operations and sample data processes. | 11/09/2023 |
| 3747 | Regeneron Tarrytown, NY Sample Management Associate BS degree Exp: 0-4 years |
Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Sample Management Associateto support biobanking operations and sample data processes. | 11/09/2023 |
| 3748 | Regeneron Tarrytown, NY Associate Scientist, Therapeutic Antibody Early Discovery BS or MS degree Exp: 0-5+ years |
Regeneron's Therapeutic Antibody Immunoscreening group is looking for a highly motivated Assoc Scientist to join our team. In this role you will contribute to the identification of potential therapeutic antibodies, in-vitro characterization and selection process of the lead molecules in early discovery stage. | 11/09/2023 |
| 3749 | Regeneron Tarrytown, NY Process Development Associate I, Bioreactor Development (1 of 3) Undergraduate degree. Exp: 0-3+ years |
Regeneron's Bioreactor Scale-Up and Development (BSD) team, a group within our Preclinical Mftg and Process Development (PMPD) organization, and which provides the link between small scale cell culture development and manufacturing, is seeking a Process Development Associate I. In this role you will assist the reagent productions to support pipeline and assay development needs for research groups and critical reagents to support GMP lot release. BSD performs cell culture up to 500 L scale and studies to support process transfer to manufacturing. | 11/09/2023 |
| 3750 | Steris Mentor, OH Quality Engineer Bachelor's Degree (In engineering or related technical field). Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 11/09/2023 |
| 3751 | Steris Conroe, TX Quality Technician Associate's Degree in Engineering General or Science. Exp: (1) year |
The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. The Quality Technician supports manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. | 11/09/2023 |
| 3752 | Steris Mentor, OH Mechanical Engineer Bachelors degree in Mechanical Engineering. Exp: one year |
The Mechanical Engineer will join a fast-paces Infection Prevention Technologies R&D team developing new Sterilizers. You will interact with other engineering disciplines and cross functional team member during the development lifecycle phases from concept development through final release. The mechanical engineering position will utilize problem solving techniques and engineering principals such as statics, machine design, thermodynamics, heat transfer, material selection and fabrication to develop solutions for medical equipment. You will be involved in 3D Modeling, Design Controls documentation, Design Verification Testing and hands-on prototyping while developing new and innovative solutions for our customers. *This position is located onsite in Mentor, Ohio with eligibility for a hybrid work schedule. | 11/09/2023 |
| 3753 | Steris Eden Prairie, MN Quality Engineer Bachelor's Degree in Engineering General or Science. Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 11/09/2023 |
| 3754 | Steris St. Louis, MO Microbiologist Bachelor degree required, with a focus in Biology or Microbiology areas required. Exp: 0-5 years |
Are you interested in contributing to a healthier and safer world? The Associate Scientist (Microbiologist) is an entry level position that is responsible for supporting new product development through innovative research and through developing technical expertise in STERIS's Infection Prevention Technology product segments, including surface disinfectants and cleaners. The Associate Scientist, with the appropriate training and guidance, will work in the lab supporting the new product development team, operations and quality to enhance the sophistication and compliance of new, unique infection prevention solutions to meet the customer’s varying unmet needs. | 11/09/2023 |
| 3755 | Steris Arlington, VA Medical Equipment Integration Technician Associate's degree in Electronics, mechanical or similar degree. Exp: one year |
Are you mechanically and technology inclined with a knack for hands-on work and love to travel? Do you enjoy working independently and thrive in a fast-paced environment where you provide an exceptional customer experience? If you want to work for a great company where you will have the opportunity to advance your career, join our growing team as an Integration Technician specializing in installing Operating Room systems to integrate all equipment, audio/visual systems, and hardware and software solutions. ***This position requires overnight travel, up to 85% of the time, Monday - Friday*** This is a remote based customer facing position. To support and service our customers in this assigned territory candidates must be based out of one of the following states: Virginia. | 11/09/2023 |
| 3756 | Steris Montgomery, AL Quality Engineer Bachelor’s Degree (Engineering or related technical field). Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 11/09/2023 |
| 3757 | BioDuro Irvine, CA Associate Scientist/Scientist, Analytical Development (Small Molecules) BS degree in Chemistry or related scientific discipline. Exp: 0-3 years’ |
The Associate Scientist/Scientist, Analytical Development independently performs analytical development activities and tasks to support formulation development and drug product manufacturing. The Associate Scientist/Scientist facilitates and assists in execution of systems to assure cGMP compliance for all relevant operations carried out within and for BioDuro, LLC. Responsible for performing advanced experiments and general laboratory duties. | 10/31/2023 |
| 3758 | BioDuro Irvine, CA Process Engineer BS degree in Engineering or Chemical Engineering preferred. Exp: 0-3 years’ |
The Process Engineer, under direct supervision, performs various duties related to optimization and analysis of production processes, new products, commercial process support and new product technology transfers. | 10/31/2023 |
| 3759 | BioDuro Irvine, CA Associate Scientist, Formulation Development BS in Chemistry or related field required. Exp: 1 year |
The Associate Scientist, Formulation Development, assists in the design and development of drug delivery systems and dosage forms. | 10/31/2023 |
| 3760 | Biomerics Salt Lake City, UT Process Engineer II Engineering Degree needed. Exp: 1-3 years |
The Process Engineer II will be responsible for supporting and improving the manufacturing of class II medical and surgical devices in a dynamic, customer-focused organization. You will be expected to work with customers to understand product and process specifications, develop manufacturing processes, and build and test devices to those specifications. All activities must be documented according to design control requirements in a design history file (DHF).P: The Process Engineer II may be an individual contributor in a small cross-functional team comprising engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. You will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team. | 10/31/2023 |
| 3761 | Biomerics Winston-Salem, NC Manufacturing Engineer I or II Engineering degree. Exp: 0-5 years’ |
The ME will be expected to lead high-impact projects. The ME is expected to lead change, contribute new ideas, and find innovative methods to accomplish goals. Work with tooling/outside suppliers/in-house personnel performing analysis of situations or data and develop an in-depth evaluation of various factors. Acts independently and exercises judgment within broadly defined practices and policies. Determines methods and procedures for new assignments. The ME will be expected to have the ability to get things done through people who do not report to them. The ME will also need to have the ability to work through adverse situations while building and maintaining good personal relationships. | 10/31/2023 |
| 3762 | Biomerics Salt Lake City, UT Process Engineer II Engineering Degree needed. Exp: 1-3 years |
The Process Engineer II will be responsible for supporting and improving the manufacturing of class II medical and surgical devices in a dynamic, customer-focused organization. You will be expected to work with customers to understand product and process specifications, develop manufacturing processes, and build and test devices to those specifications. All activities must be documented according to design control requirements in a design history file (DHF). The Process Engineer II may be an individual contributor in a small cross-functional team comprising engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. You will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team | 10/31/2023 |
| 3763 | Biomerics Salt Lake City, UT Lab Technician I - II Lab Technician I typically requires an associate or bachelor’s degree. Lab Technician II typically requires a bachelor’s degree in chemistry or a rela Exp: 1+ years |
Performs analytical and functional testing. Maintains glassware by picking up, cleaning, washing, sterilizing, and distributing. Keeps laboratory supplies ready by inventorying stock, placing orders, and verifying receipts. Keeps equipment operating by following operating instructions. Troubleshoots breakdowns maintains supplies, performs preventive maintenance, and calls for repairs—documents information by maintaining daily logs and equipment record books. Resolves problems by examining and evaluating data; select corrective steps. | 10/31/2023 |
| 3764 | PSC Biotech Remote Job, CSV Engineer I - Remote Job Bachelor’s degree in Computer Science, Engineering, or a related field. Exp: 1-3 years |
We are hiring motivated and passionate entry to junior level Computer Systems Validation Engineers to join our team. The successful candidate will have excellent communication and interpersonal skills, strong analytical and problem solving skills, and a strong drive to learn. While this is a remote position, candidates in Midwest and/or Pacific Time Zones are preferred. | 11/01/2023 |
| 3765 | PSC Biotech York, PA Manufacturing Associate I Associates Degree in Life Sciences/Liberal Arts field preferred. Exp: 1-3 years |
This position is responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMP/ISO requirement and standards as defined in FDA and EU applicable Regulations. With general supervision the individual will perform routine and critical manufacturing operations, including but not limited to work functions in aseptic and non-aseptic filling, equipment prep, cleaning dissolution and formulation activities. The individual may provide support in other departments within the company, including but not limited to, engineering, warehouse and facilities. The incumbent is also responsible and accountable for the execution of the PSC BioTechnique mission, “to maintain the integrity and professionalism of our products and services while enabling steady growth and development”. | 11/01/2023 |
| 3766 | Biotium Fremont, CA Chemistry Technician I (CHEMISTRY) B.S. or M.S. degree in Chemistry. Exp: 1+ years |
Under the direct supervision from a senior chemist, perform chemical purifications using chromatography including preparative HPLC or gravity chromatography; carry out chemical synthesis using standard protocols; carry out chemical analyses using modern instruments including analytical HPLC, LC-MS, TLC, UV/Vis and fluorescence spectrophotometry. | 11/02/2023 |
| 3767 | Biotium Fremont, CA Research Associate I, BIOSCIENCE B.S. or M.S. in Biology, Molecular Biology, Biochemistry or a related field. Exp: 1+ years |
Under supervision from Biotium scientists, perform biological testing of fluorescent dyes and related reagents. Perform production and quality control testing of assay kit components following standardized protocols. | 11/02/2023 |
| 3768 | Shape Therapeutics Seattle, WA Research Associate/Senior Research Associate, Research Technologies BS degree in Molecular Biology, Cellular Biology, Biochemistry, or a closely related field. Exp: one year |
ShapeTX is seeking a highly motivated Research Associate/Senior Research Associate (RA/SRA) to join our Research Technologies Team. This is an excellent opportunity for a motivated individual with demonstrated molecular biology expertise to contribute to the advancement of our RNAfixTM technology. In this multifaceted position, you will be at the forefront of developing innovative gene therapy payload designs for ShapeTX's disease programs, with responsibilities encompassing independent cloning of plasmids and constructs, employing techniques such as PCR, plasmid ligation, bacterial transformation, and DNA/RNA isolation. You will also play a pivotal role in evaluating novel payloads through tissue culture and transfection-based experiments while maintaining meticulous lab organization and communicating results effectively within our dynamic research environment. This role presents a unique chance to join the critical core of our Research Technologies Team within a rapidly growing biotechnology startup, offering substantial opportunities to contribute to groundbreaking biological applications addressing serious human diseases. | 11/02/2023 |
| 3769 | Shape Therapeutics Seattle, WA Research Associate/Senior Research Associate, AAV Purification - Cell, Assay, and Vector Engineering BS/MS in molecular/cellular biology or other relevant scientific discipline. Exp: 1-5 years |
ShapeTX is looking for a highly motivated individual with a strong passion for learning to join the growing Research team as Research Associate/Senior Research Associate, AAV Purification - Cell, Assay, and Vector Engineering. In this role, the successful candidate will purify and characterize AAV to support the early research pipeline and ShapeTX’s novel RNAfixTM and RNAskipTM technology platforms. The candidate will conduct exploratory research to develop novel AAV purification methods in addition to routine purifications. An ideal candidate will have demonstrated AAV/viral purification experience or broad recombinant protein purification experience a collaborative spirit, and a desire to work in a fast-paced startup environment. | 11/02/2023 |
| 3770 | Shape Therapeutics Seattle, WA Research Associate/Senior Research Associate, Virus Production and Engineering BS/MS in molecular/cellular biology or other relevant scientific discipline. Exp: 1/3 years |
ShapeTX is looking for a highly motivated individual with a strong passion for learning to join the growing Research team as a Research Associate/Senior Research Associate, Virus Production and Engineering. In this role, the successful candidate will generate AAV to support the early research pipeline and ShapeTX’s novel RNAfixTM and RNAskipTM technology platforms. An ideal candidate will have broad cell culture experience, an understanding of molecular biology techniques, a collaborative spirit, and a desire to work in a fast-paced startup environment. | 11/02/2023 |
| 3771 | Boston Analytical Salem, NH Quality Assurance Specialist I Bachelor’s degree in a related science discipline. Exp: 0-1 years |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing chemists analytical data, routine work, protocols and reports. | 11/02/2023 |
| 3772 | Boston Analytical Salem, NH Analytical Chemist Bachelor’s degree in Chemistry or a related science discipline is required. Exp: 0-2 years |
The Analytical Chemist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 11/02/2023 |
| 3773 | Boston Analytical Salem, NH QC Microbiologist BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 11/02/2023 |
| 3774 | Boston Analytical Salem, NH Microbiologist - Environmental Monitoring BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The EM Microbiologist conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 11/02/2023 |
| 3775 | Boston Analytical Framingham, MA Offsite EM Technician Associates degree preferred. Science classes or an associates degree in a scientific discipline is preferred. Exp: 0+ years |
The Offsite Environmental Monitoring Technician will perform Environmental Monitoring (EM) of pharmaceutical cleanrooms and the associated spaces on a daily basis according to FDA, cGMP and Boston Analytical's/Client Standard Operating Procedures. The position is primarily in the Framingham, MA area. | 11/02/2023 |
| 3776 | Boston Institute of Biotechnology Southborough, MA Research Associate - Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≤1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision. | 11/03/2023 |
| 3777 | Boston Institute of Biotechnology Southborough, MA Research Associate - Upstream Process Development BS degree in Biochemical Engineering or related field of study. Exp: 0-2 years |
Responsibilities 1. Set up, execute, and monitor microbial and mammalian cell culture production in fermenters and bioreactors. 2. Collect, record, and report experimental data. 3. Provide updates to a team lead on a regular basis. 4. Maintain all notebooks and documentation according to department standards. 5. Write SOPs, and batch records. 6. Ability to work well in a team environment and independently as required. 7. Ensure and promote safe environmental and laboratory practices. 8. Order supplies as needed. 9. Prepare solutions and buffers. 10. Maintain lab space and equipment. | 11/03/2023 |
| 3778 | Boston Institute of Biotechnology Southborough, MA Research Associate - Analytical Development Bachelor’s or Master’s degree in Biology, Chemistry, Pharmaceutical Sciences, or a related/relevant discipline. Exp: Entry Level |
The Research Associate role within Analytical Development is an entry level position for individuals with a Bachelor’s or Master’s degree. Responsibilities include developing analytical methods for biologics characterization, characterizing samples from process development, and supporting subsequent clinical and/or commercial GMP manufacturing. | 11/03/2023 |
| 3779 | BostonGene Waltham, MA Research Associate, Molecular Biology & Next Generation Sequencing Bachelor’s (B.S.) degree in biology, clinical laboratory science, medical technology, or related discipline. Exp: 0-2 years |
BostonGene is seeking a highly motivated Research Associate to join our R&D team in our laboratory located in Waltham, MA. This candidate will support BostonGene’s state-of-the-art primary next-generation sequencing (NGS), adjunct analytical platforms, and automated analysis pipelines. The candidate will be expected to develop proficiencies in NGS support protocols, such as RNA and DNA isolation from tissue, cell-free DNA isolation from plasma, Whole Exome and RNA-Seq library preparation, qPCR, Molecular Biology techniques, and other sample QC techniques | 11/03/2023 |
| 3780 | Boundless Bio San Diego, CA Research Associate, HTS Screening, Drug Discovery BS/MS in biology related field. Exp: 1 year |
As a Research Associate at Boundless Bio, you will play a significant role in helping us transform exciting extrachromosomal DNA (ecDNA) discoveries into cancer medicines of the future. You will contribute to the process of developing robust, miniaturized high-throughput assays designed to enable drug discovery programs supporting multiple ecDNA-directed targets. This will involve broad application of biochemical and cellular assays across a range of formats to enable screening and SAR campaigns in support of our drug pipeline. These efforts will make an important contribution to the Boundless Bio drive for innovation in targeting difficult to treat cancers. | 11/03/2023 |
| 3781 | BPS Bioscience San Diego, CA Research Scientist I - Cell Biology M.S Exp: 1+ years |
BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, lentiviruses, and recombinant cell lines for drug discovery. We are currently seeking a diligent and highly motivated scientist to join our cell biology group to assist in production and new product development. | 11/03/2023 |
| 3782 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required. Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 11/03/2023 |
| 3783 | Cabaletta Bio Philadelphia, PA Sr. Research Associate/Associate Scientist Molecular Biology M.S. degree in Life Sciences or closely related discipline. Exp: 1 -2 years |
Reporting to the Associate Director, Molecular Biology group, we are seeking an experienced and motivated Senior Research Associate or Associate Scientist. Under scientific and technical supervision, the candidate will design and produce molecular constructs that could be utilized for vector development and protein production. The individual will focus and work along for manufacturing small and large scale LVV gene therapy vectors across various preclinical programs and disease areas. The position offers growth into additional areas such as cell biology and molecular biology, immunology, and cell therapy. The position involves both technical and operational responsibilities. | 11/03/2023 |
| 3784 | Bayer Berkeley, CA Associate Electric Engineer M.S. Degree in Electrical Engineering or related discipline. Exp: 0-1 years |
Exciting and challenging electrical engineering opportunity where each day is different. Tasks would include evaluating electrical capacity, emergency power readiness, equipment maintenance, alternative sustainable energy solutions, and component electrical ratings analysis. Interact with cross-functions including Quality, Production, Procurement, Investment Management, Research and Development at the at the local, regional, and global levels as well as external vendors, and CA state supplier. | 11/03/2023 |
| 3785 | Bayer Pittsburgh, PA Manufacturing Associate II - O'Hara M-TH 5:30am-3:50pm Associate's Degree Exp: 1+ years |
This advanced position exists to provide experienced resources to assemble and support the various medical device manufacturing processes. It also provides a supporting role in the way of quality control in combination with advanced assembly, performed in a timely manner to meet quality and productivity goals of the department. This role will also assist the process coordinator or group lead in any training or cross training efforts as needed. The role will also interact between many departments to transmit information and recommend solutions to design, process and quality problems/non-problems. Leadership, a positive attitude and willingness to support teamwork is key! This role provides mentorship and support to the Manufacturing Production floor personnel in any way possible! This position will incorporate both Assembly and Quality inspections and requires more than one years’ experience at Bayer or in a position with related work experience | 11/03/2023 |
| 3786 | Bayer Luling, LA Chemical Production Engineer Bachelor’s of Science degree in Chemical Engineering, including May 2024 B.S. Chemical Engineering graduates. Exp: Up to 3 years |
The Chemical Production Engineer provides support to plan, coordinate, and execute technical activities needed to support manufacturing operations. Also, ensures the safe, efficient, productive, and environmentally sound manufacture of active ingredients or intermediates. | 11/03/2023 |
| 3787 | Bayer Berkeley, CA Associate Electrical Engineer M.S. Degree in Electrical Engineering or related discipline. Exp: 0-1 years |
Exciting and challenging electrical engineering opportunity where each day is different. Tasks would include evaluating electrical capacity, emergency power readiness, equipment maintenance, alternative sustainable energy solutions, and component electrical ratings analysis. Interact with cross-functions including Quality, Production, Procurement, Investment Management, Research and Development at the at the local, regional, and global levels as well as external vendors, and CA state supplier. | 11/03/2023 |
| 3788 | Abcam Waltham, MA Laboratory Technician - Proteins Associate's degree. Exp: one year |
Abcam is looking for a Lab Technician to join our team in Waltham MA, working to support the Protein Science team in the development of standalone recombinant products at Abcam. The goal of this product line is to deliver outstanding products to our customers and help Abcam achieve our aim of being the most influential company in life sciences by helping advance global understanding of biology and causes of disease, which, in turn, will drive new treatments and improved health. | 11/03/2023 |
| 3789 | Abcam Eugene, OR Research Associate - Biochemical Assay Design Bachelor's degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 1+ years |
Abcam, a leading life sciences company, is seeking a motivated and detail-oriented individual to join our team as a Research Associate - Biochemical Assay Design in our Eugene, Oregon location. If you are passionate about advancing research in the life sciences and possess a strong background in biochemical assays, we encourage you to apply. | 11/03/2023 |
| 3790 | Agilent Carpinteria, CA Histology Laboratory Assistant Bachelors in biological sciences preferred. Exp: 1+ years |
The position will support the tissue procurement department and will include tasks and documentation to move new donor samples through incoming quality control to delivery of qualified samples to internal teams. This laboratory assistant position will have duties both in the lab and at the desk. | 11/03/2023 |
| 3791 | Bio Marin Pharmaceutical San Rafael, CA Research Associate (Temporary) Master’s degree in a scientific discipline or equivalent. Exp: 1 to 3 years |
We are searching for a talented and highly motivated Research Associate II to develop assay methods that will provide safety and efficacy data on experimental therapeutics entering clinical studies. The candidate will be responsible for the development of assays for diverse drug modalities, which may include gene therapies, monoclonal antibodies, oligonucleotides, biologics, and small molecules, with guidance from a Scientist in the Assay Strategy and Development group. The ideal candidate should have experience developing and optimizing bioanalytical methods, analyzing and interpreting experimental results, and communicating conclusions to other scientists. The successful candidate will participate in programs that range from exploratory in vitro and animal studies to non-clinical efficacy and safety studies and clinical trials. You will be responsible for developing new methods, evaluating novel technologies, conducting translational research internally at the BioMarin Research Center and externally in partnership with contract research organizations, and communicating results to cross-functional teams. This position offers a unique opportunity to interact with scientific and business colleagues across many functional areas, including Research, Translational Sciences, Regulatory Affairs, and Clinical Sciences. This RA II position will report to a Scientist in the Assay Strategy and Development group and will have the opportunity to advance our most promising pipeline programs to treat rare genetic diseases. | 11/03/2023 |
| 3792 | Bio Marin Pharmaceutical San Rafael, CA Research Associate II, Molecular Medicine, Translational Sciences Master’s degree in Biology, Chemistry, or like field. Exp: 0-2 yr |
The Molecular Medicine Group within the Translational Sciences Department at BioMarin Pharmaceutical is seeking a Research Associate II to help drive understanding of the underlying mechanisms for successful treatment with recombinant Adeno Associated Viral (rAAV) gene therapy and antisense oligo (ASO) modalities. The ideal candidate has a flexible mindset, natural curiosity and motivation to understand biology at the molecular and biochemical levels. The Molecular Medicine group aims to creatively apply the complete molecular and cellular toolkit to understand the contributing mechanisms of action or effect, in collaboration with colleagues across the company. We are positioned to help solve technically challenging questions that present as unexpected findings and/or have cross-program impact. We are currently particularly interested identifying early indicators and mechanisms that modulate the magnitude, durability and variability of expression of our gene therapy candidate(s). We work with cross-functional teams to develop and evaluate nucleotide integration capabilities for safety assessments. The Molecular Medicine group strives to improve technologies to enable analysis on small samples with definitive results, including at the single cell and nuclei level. The group collaborates with the entire set of Translational Sciences functions to understand the molecular and cellular actions of our therapeutics in preclinical experiments through clinical delivery to our patients. As our expanding clinical stage pipeline evolves, this RAII will have the opportunity to contribute to molecular investigations on a variety of therapeutic modalities and the genetic diseases that BioMarin strives to treat. This position will be primarily laboratory focused. The Research Associate II will be responsible for the design and execution of technically complex experiments to support multiple projects, with strategic input and guidance from Molecular Medicine and Translational Sciences leadership. S/he will provide quantitative data analysis, interpretation of results, and contribute to technical reports and scientific papers. S/he will evaluate existing complex methods and technologies, develop new solutions, and collaborate across functions to solve technical problems. The Molecular Medicine team values learning agility, open communication skills, willingness to support others’ experiments, and ability to trouble-shoot experiments on multiple platforms. The SRAII al | 11/03/2023 |
| 3793 | Bio Marin Pharmaceutical San Rafael, CA Research Associate II, Assay Strategy and Development (Temporary) Master’s degree in a scientific discipline or equivalent. Exp: 1 to 3 years |
We are searching for a talented and highly motivated Research Associate II to develop assay methods that will provide safety and efficacy data on experimental therapeutics entering clinical studies. The candidate will be responsible for the development of assays for diverse drug modalities, which may include gene therapies, monoclonal antibodies, oligonucleotides, biologics, and small molecules, with guidance from a Principal Scientist in the Assay Strategy and Development group. The ideal candidate should have experience developing and optimizing bioanalytical methods, analyzing and interpreting experimental results, and communicating conclusions to other scientists. The successful candidate will participate in programs that range from exploratory in vitro and animal studies to non-clinical efficacy and safety studies and clinical trials. You will be responsible for developing new methods, evaluating novel technologies, conducting translational research internally at the BioMarin Research Center and externally in partnership with contract research organizations, and communicating results to cross-functional teams. This position offers a unique opportunity to interact with scientific and business colleagues across many functional areas, including Research, Translational Sciences, Regulatory Affairs, and Clinical Sciences. This RA II position will report to a Principal Scientist in the Assay Strategy and Development group and will have the opportunity to advance our most promising pipeline programs to treat rare genetic diseases. | 11/03/2023 |
| 3794 | Bristol-Myers Squibb Phoenix, AZ Associate, QC Microbiology Operations Bachelor’s Degree in a scientific field preferred. Exp: 0-2 years’ |
2nd Shift- 2pm.-10:30pm. Position: EG 70-Associate, QC Microbiology Operations Location: Phoenix, AZ At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. | 11/03/2023 |
| 3795 | Bristol-Myers Squibb Devens , MA Manufacturing Associate II, Cell Therapy (12-hour shifts) Bachelors in relevant science or engineering discipline. Exp: 1+ years |
BMS Cell Therapy Manufacturing seeks an Associate II within Manufacturing that brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The candidate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind. We are searching for enthusiastic, and innovative individuals with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. | 11/03/2023 |
| 3796 | Bristol-Myers Squibb Devens , MA Bioprocess Associate (Night Shift) B.S., in science, engineering, biochemistry or related discipline, or its equivalent is desired but not required. Exp: 1+ years |
The Bioprocess Associate assists in the execution of commercial manufacturing processes according to established electronic work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs). *This is a rotating night shift position (5pm-5am), therefore eligible for a 20% shift differential. | 11/03/2023 |
| 3797 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree. Exp: 0-2 years |
We are seeking an Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 10/23/2023 |
| 3798 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
We are seeking an Advanced Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 10/23/2023 |
| 3799 | Advanced Cell Diagnostics Minneapolis, MN RA - Advanced Research Associate Master’s degree. Exp: 1+ years |
Position Summary In this role, you would be responsible for the development and execution of QC test method validations for a variety of products, utilizing a wide variety of laboratory techniques. This position also assists in troubleshooting investigations and process improvement projects. As an Advanced Research Associate, you will also participate in cross-functional teams focused on new product introduction. | 10/23/2023 |
| 3800 | Advanced Cell Diagnostics Minneapolis, MN RA - Research Associate Bachelor’s degree in a related field. Exp: up to 3 years |
Position Summary: This position is responsible for participating in the development of Bio-Techne's various product lines. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 10/23/2023 |
| 3801 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
POSITION SUMMARY This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 10/23/2023 |
| 3802 | Advanced Cell Diagnostics Minneapolis, MN Research Associate - Protein Purification Development Bachelor’s degree in Biology or related field. Exp: up to 5 years |
Position Summary: We seek a highly motivated and creative individual to join our protein purification development team. Our team is responsible for the development of Bio-Techne's various product lines, with a focus on the high-quality recombinant protein products. You will participate in the development and optimization of protein purification procedures for recombinant proteins expressed in various cell lines (E. coli, baculovirus, and mammalian). In addition, you will also assist with initial, small-scale production for release of newly developed proteins and redevelopment of existing products to help advance Bio-Techne's evolving portfolio. This is a great opportunity to gain experience with cutting-edge biotech development/manufacturing processes & practices while working in a collaborative laboratory environment. | 10/23/2023 |
| 3803 | Advanced Cell Diagnostics Minneapolis, MN Research Associate, Analytical QC B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
Position Summary: As the Research Associate, Analytical Quality Control Analyst you will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include concentration determination, SDS-PAGE with densitometry, endotoxin assay, PCR, HABA, conductivity, total organic carbon and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis, and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned. | 10/23/2023 |
| 3804 | Akouos Boston, MA Engineer, Downstream Process Development - Akouos M.S in Biochemistry, Chemical Engineering, Bioengineering or related discipline. Exp: 1+ years |
The Process Development group at Akouos is seeking an innovative Engineer to provide hands-on development support for the manufacturing of AAV-based gene therapy vectors. The ideal candidate for this position is an entry level Engineer with a background in AAV vector purification technologies and gene therapy downstream process development. The successful candidate will actively participate in downstream process development, scale-up, process optimization, and process tech transfer for GMP manufacturing. The successful candidate will thrive in a collaborative, scientifically stimulating, and fast-pace work environment. | 10/25/2023 |
| 3805 | Akouos Indianapolis, IN Chemist- Nucleic Acid Synthesis Bachelor's and/or Master's degree Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 10/25/2023 |
| 3806 | Akouos Branchburg, NJ Engineer - Technical Services/Manufacturing Science BS degree in Chemistry, Microbiology, Biochemistry or related science, or BS in Chemical Engineering or related engineering discipline. Exp: 0-3 years |
This position is responsible for the technical support of manufacturing operations. This position will interact with the engineering, manufacturing, validation, quality assurance, quality control and regulatory departments. Interaction may be required with other Lilly site / contract producers of Lilly products. Knowledge of cell culture, purification and support systems used in the manufacturing of biotech products is required. Spreadsheet experience is required. Database experience a plus. | 10/25/2023 |
| 3807 | Alexion Pharmaceuticals Cambridge, MA Associate Scientist Masters Degree Exp: 1-2 years |
The Genomic Medicine group at Alexion Pharmaceuticals, AstraZeneca Rare Disease, has an outstanding opportunity for an Associate/Senior Associate position within the Genomic Medicine Group. We seek a highly motivated, curious, and detail-oriented individual with strong technical and problem-solving skills that would like to join our Rare Neurological and Rare Neuromuscular disorders team. The candidate will contribute to data generation, collaborate in discovering high-quality drug candidates, and will help build data packages to advance programs to IND. | 10/25/2023 |
| 3808 | Alexion Pharmaceuticals Cambridge, MA Senior Associate Scientist, Biology Master’s degree in Biology Exp: 1-2 years |
We are seeking a dedicated and innovative Senior Associate Scientist or Scientistto join our Genomic Medicine group at Alexion, AstraZeneca Rare Disease. The successful candidate will be a key member of the Alexion Genomic Medicine Cardiology team. The group’s mission is to discover and deliver transformational genomic medicines to patients with rare genetic cardiomyopathies. We are looking for a candidate with a background in cellular and molecular biology. In this role, you will be mainly responsible for developing and implementing a range of molecular and functional assays to assess the disease process, discover new medicines, and evaluate their therapeutic potential using human induced pluripotent stem cell derived cardiomyocytes (HiPSC-CMs). Additionally, you will be part of cross-functional teams and state of the art technology cores, and your scientific contributions will help advance Alexion’s preclinical programs to the clinic. | 10/25/2023 |
| 3809 | Alexion Pharmaceuticals Cambridge, MA Senior Associate Scientist, Biology Master’s degree in Biology Exp: 0-2 years |
We are seeking a dedicated and innovative Senior Associate Scientist to join our Genomic Medicine group at Alexion, AstraZeneca Rare Disease. The successful candidate will be a key member of the Alexion Genomic Medicine Cardiology team. The group’s mission is to discover and deliver transformational genomic medicines to patients with rare genetic cardiomyopathies. We are looking for a candidate with a background in molecular biology and experience with mammalian cell culture. In this role, you will be responsible for developing and performing molecular and immunoassays in samples collected from cells or mammalian in vivo models. With the support of cross-functional teams and state of the art technology cores, your scientific contributions will help advance our preclinical programs to the clinic. | 10/25/2023 |
| 3810 | Alexion Pharmaceuticals Cambridge, MA Senior Associate Scientist Master's Degree in cell biology and/or disease biology, pharmacology. Exp: 1-2 years |
We are searching for a dedicated and innovative Senior Associate Scientist to enhance our genomic medicine within Alexion, AstraZeneca Rare Disease. The chosen candidate will assume a pivotal role as a valuable member of the Alexion Genomic Medicine Cardiology team. Our mission revolves around pioneering genomic treatments for patients facing rare genetic cardiomyopathies. We are particularly interested in applicants with a robust background in pharmacology and disease biology. In this position, you will utilize your expertise in cardiac physiology to validate targets, plan and execute critical pre-clinical efficacy and safety studies, supporting the development of cardiac gene therapies from pre-clinical research to clinical development. You will collaborate closely with the biology lead, contributing preclinical in vivo data to ensure project timelines are met. | 10/25/2023 |
| 3811 | Alturas Analytics Moscow, ID Assistant Scientist Bachelor’s degree in a physical, biological or chemistry science required. Exp: 1-3 years |
The Assistant Scientist provides support to other laboratory personnel through a variety of duties and tasks. This is an entry-level position used to train all Associate Scientists. | 10/26/2023 |
| 3812 | Ampac Analytical Petersburg, VA Process Scientist III master's degree Exp: 0-3 years |
The Process Scientist is responsible for plant production support and the process development of pharmaceutical ingredients. Work is closely supervised. | 10/26/2023 |
| 3813 | Arbor Technologies Cambridge, MA Research Associate, In vivo Pharmacology, CNS MS degree Exp: 0-2 years |
The CNS Team at Arbor Biotechnologies is looking for a Research Associate interested in functioning at the cross section of technology and therapeutics. Our team is leveraging the strength of Arbor’s discovery platform to advance the cutting-edge CNS therapeutics utilizing in vitro and in vivo model systems. Arbor is a highly collaborative environment, and you will have the opportunity to work closely with the discovery, computation, and protein engineering teams, as well as to continue to explore new techniques for your professional growth. This role is at the forefront of Arbor’s translational evolution and will be given an opportunity to solidify the understanding of our assets for internal and external therapeutic development. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in an innovative company. Working at Arbor offers a unique opportunity that combines the fast pace and growth opportunities of a startup with the intellectual rigor and creativity of academia. A successful candidate in this position will be responsible for executing biodistribution and pharmacology/efficacy studies in mouse models of neurological/neuromuscular disease. You will also perform ex vivo tissue analyses from in vivo studies, including but not limited to tissue processing and molecular assessments. The ideal candidate will have direct experience in animal handling and dosing. | 10/26/2023 |
| 3814 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Translational Biomarkers BS Exp: 1 year |
Arrowhead is seeking an Associate Scientist to join our growing Biology Department at our Madison site. This is an excellent opportunity to utilize, contribute and advance the ideal candidate’s laboratory skills in a progressive, state-of-the-art and diverse facility. | 10/27/2023 |
| 3815 | Arrowhead Pharmaceuticals San Diego, CA Associate Scientist, Bioconjugation B.S. or M.S. Chemistry or Biochemistry degree Exp: 0-8 years |
Arrowhead is seeking a highly motivated Associate Scientist to join our growing discovery chemistry team at our San Diego site. He/She will primarily focus on oligonucleotide bioconjugation, purification, analytical chemistry. As a siRNA chemistry bioconjugation specialist, you will play a pivotal role in the development and optimization of siRNA-based therapeutics by leveraging your expertise in bioconjugation strategies and siRNA chemistry. | 10/27/2023 |
| 3816 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Small Scale Synthesis B.S. Chemistry or Biochemistry degree Exp: 0-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Chemist to join the Discovery Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, purification, analytical chemistry, and contributing to specific program goals. S/He will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 10/27/2023 |
| 3817 | Ascent Pharmaceuticals Central Islip, NY Analytical Chemist Bachelor’s degree or foreign equivalent in Pharmacy/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Analytical Chemists for our Central Islip, NY location to develop, validate and conduct inter laboratory transfer of analytical methods for active pharmaceutical ingredients (API) and dosage forms; validate analytical methods and perform quality control activities; research & develop efficient and selective analytical procedures and draft/review laboratory SOPs; design, evaluate and monitor stability programs for drug products; work with advanced analytical equipment; supervise and train chemists and laboratory personnel; test drug substances, intermediates and raw materials while conducting impurity profiles for drug substances and intermediates; prepare ANDAs for FDA submissions etc. | 10/27/2023 |
| 3818 | Ascent Pharmaceuticals Central Islip, NY Quality Control Chemist Bachelor’s degree or foreign equivalent in Pharmacy/ Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Quality Control Chemists in our Central Islip, NY location to collaborate with multiple departments including Manufacturing, Facilities, Engineering, Quality Control, Validation, Quality Assurance, and Regulatory to facilitate agreement on equipment, initiation and execution of Product development projects (ANDA Projects), process operational parameters, test requirements and acceptance criteria; Execute Change Controls to allow for the ongoing maintenance and optimization of validated systems and report KPI’s to higher management; Review and approve of a variety of validation lifecycle documents, project plans, user requirement specifications, SOPs, maintenance documentation, investigation reports, deviation resolution, CAPA closeout, etc.; Conduct internal & vendor audits in a group setting & under guidance from senior chemists/scientist for compliance with SOP, CGMP & FDA requirements. Research new regulatory guidance and cGMP and prepare reports for senior scientists and department heads to review and assist in drafting SOP’s; Critically evaluate current processes and continually identify ways to save time and money without sacrificing product quality; Investigate product, and process deviations, identify root cause, and develop corrective and preventative actions; Participate in audits by customers and regulatory agencies and respond to customer complaints in timely manner, review and close out market enquiries & investigations; Assist in APQR, Deviation & Investigation, Risk Assessment, CAPA Management, Change control management, Root Cause Investigation with SPC tools, Market Complaint Handling, Adverse event investigations; Review and Report Process Characterization Protocols, Equipment Qualifications, and review Process Validations of various ANDA drug projects; Conduct internal audits for compliance with SOP, cGMP & FDA requirements. | 10/27/2023 |
| 3819 | Ascent Pharmaceuticals Central Islip, NY Qiality Assurance Chemist Bachelor’s degree or foreign equivalent in Science/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Quality Control Chemists in our Central Islip, NY location to collaborate with multiple departments including Manufacturing, Facilities, Engineering, Quality Control, Validation, Quality Assurance, and Regulatory to facilitate agreement on equipment, initiation and execution of Product development projects (ANDA Projects), process operational parameters, test requirements and acceptance criteria; Execute Change Controls to allow for the ongoing maintenance and optimization of validated systems and report KPI’s to higher management; Review and approve of a variety of validation lifecycle documents, project plans, user requirement specifications, SOPs, maintenance documentation, investigation reports, deviation resolution, CAPA closeout, etc.; Conduct internal & vendor audits in a group setting & under guidance from senior chemists/scientist for compliance with SOP, CGMP & FDA requirements. Research new regulatory guidance and cGMP and prepare reports for senior scientists and department heads to review and assist in drafting SOP’s; Critically evaluate current processes and continually identify ways to save time and money without sacrificing product quality; Investigate product, and process deviations, identify root cause, and develop corrective and preventative actions; Participate in audits by customers and regulatory agencies and respond to customer complaints in timely manner, review and close out market enquiries & investigations; Assist in APQR, Deviation & Investigation, Risk Assessment, CAPA Management, Change control management, Root Cause Investigation with SPC tools, Market Complaint Handling, Adverse event investigations; Review and Report Process Characterization Protocols, Equipment Qualifications, and review Process Validations of various ANDA drug projects; Conduct internal audits for compliance with SOP, cGMP & FDA requirements. | 10/27/2023 |
| 3820 | Asha Pharma San Diego, CA SR./RESEARCH ASSOCIATE (SAN DIEGO, CA) BS/MS degree in Chemical Engineering, Materials Science, Chemistry, Pharmaceutical Science or related field. Exp: 0-2 years’ |
This position involves working in a laboratory that evaluates novel chemical compounds (typically pharmaceuticals) and discovers novel crystalline structures of the same as part of drug development. The Sr./Research Associate will independently work on projects related to crystallization R&D (e.g. polymorph, salt, cocrystal screening and crystallization process development for pharmaceutical and other molecules) under the guidance of a senior team member. The Sr./Research Associate will also help with Business Development Activities, providing a unique opportunity for well-rounded career development. | 10/27/2023 |
| 3821 | Astellas Westborough, MA Research Associate II, Analytical Development MS Exp: 0-2 years |
The Research Associate II will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOP’s and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 10/27/2023 |
| 3822 | Astellas Westborough, MA Research Associate II, Analytical Development MS Exp: 0-2 years |
The Research Associate II will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOP’s and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 10/27/2023 |
| 3823 | Astellas Westborough, MA Research Associate II, Analytical Development MS Exp: 0-2 years |
The Research Associate II will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOP’s and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 10/27/2023 |
| 3824 | Astellas Westborough, MA QC Analyst I, Analytical B.S. degree in Biology/ or other life science related degree. Exp: 0-3 years |
Astellas, Westborough is seeking a highly motivated individual with strong organizational skills to join us as a QC Analyst I, Analytical. This position provides Quality Control compliance and testing support for Astellas cell therapy products. Looking for a strong GMP and scientific background and experience with quality control testing of cell therapies. | 10/27/2023 |
| 3825 | Astellas Seattle, WA Research Associate II, Stem Cell Therapies MS Exp: 0-2 years |
This Research Associate II position is a laboratory focused role with the primary purpose of providing support toward the development of novel stem cell derived cellular therapies. This position will work primarily in a laboratory setting with Scientists and R&D teams. | 10/27/2023 |
| 3826 | Astellas Seattle, WA Research Associate II, Core Technologies MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department . This individual will contribute to the molecular engineering for our gene edited Universal Donor Cells with activities focused on performing custom TaqMan based PCR assays. They will work as a key member on a fast-paced team to run molecular assays to characterize our proprietary Universal Donor Cells. | 10/27/2023 |
| 3827 | Astellas Sanford, NC Analyst II, QC Biochemical Operations M.S. degree in Biological Sciences Exp: 0-3+ years |
The Analyst II, QC will be responsible for implementing and executing analytical testing in support of clinical and commercial viral vector products in compliance with GMP requirements. Will also support testing for stability studies, methods validation studies and equipment validation. This position typically reports to the Manager, QC Biochemical Ops. | 10/27/2023 |
| 3828 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters in science related field. Exp: 0-1 year |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 10/27/2023 |
| 3829 | Avedro San Clemente, CA Manufacturing Technician II - Glaukos bachelor’s degree in science or engineering Exp: 0 – 2 years’ |
The Manufacturing Technician II, based in San Clemente, CA, will perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality system regulation (QSR) medical device good manufacturing practices (GMP) requirements. | 10/27/2023 |
| 3830 | Azzur San Diego, CA Lab Technician II Associate’s or Bachelor's degree in Microbiology or related science. Exp: 1-2 years |
The LabTech II performs laboratory procedures related to Sample Receipt, Media Prep, Shipping and Receiving of Material, and Lab cleaning and maintenance. Lab Tech I has the responsibility to perform duties following established methods and protocols. | 10/27/2023 |
| 3831 | Azzur Schnecksville, PA Quality Specialist I Bachelor of Science or Bachelor of Arts in a science or engineering field. Exp: 1 - 3 years |
Azzur Labs is seeking a Quality Specialist I for their PA Laboratory. The Quality Specialist I supports the company’s quality assurance and control programs. The Quality Specialist I is responsible for document review and control, inventory control, and quality control of incoming materials. The Quality Specialist I will assist the Quality Manager in assuring that the quality management system is implemented and followed. | 10/27/2023 |
| 3832 | Azzur Devens, MA Quality Specialist I Bachelor of Science or Bachelor of Arts in a science field. Exp: 1-2 year |
Azzur Labs is seeking a Quality Specialist for their Boston Laboratory. The Quality Specialist I supports the company’s quality assurance and control programs. The Quality Specialist I is responsible for document review and control, inventory control, and quality control of incoming materials. The Quality Specialist I will assist the Quality Manager in assuring that the quality management system is implemented and followed. | 10/27/2023 |
| 3833 | Azzur Alameda, CA Quality Specialist I Bachelor of Science or Bachelor of Arts in a science or engineering field. Exp: 1 - 3 years |
Azzur Labs is seeking a Quality Specialist I for their CA Laboratory. The Quality Specialist I supports the company’s quality assurance and control programs. The Quality Specialist I is responsible for document review and control, inventory control, and quality control of incoming materials. The Quality Specialist I will assist the Quality Manager in assuring that the quality management system is implemented and followed. | 10/27/2023 |
| 3834 | Beam Therapeutics Research Triangle Park, NC Manufacturing Associate (Multiple Openings) BS, MS a plus, in Life Sciences or Engineering. Exp: 0-5 years |
Beam is expanding our geographical footprint to RTP, NC with the recent announcement of a 100,000 square foot manufacturing facility in addition to our laboratory-based facilities located in Cambridge, MA. We are looking for highly energetic Manufacturing Associates to support start-up and scaling of cGMP manufacturing at our new RTP site. The successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and start-up. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment. | 10/27/2023 |
| 3835 | Berkshire Sterile Manufacturing Lee, MA QC Analytical Associate I Bachelor’s Degree Exp: Zero to two (0-2) years |
The Quality Control Analytical Associate performs laboratory testing and administrative tasks for the QC department. Testing includes incoming materials, in-process samples, finished good and stability samples. It also includes performing experiments for method transfers, qualifications and validation. The QCA Analyst is responsible for creating and revising documents related to testing such as SOPs, test methods, protocols and reports. The position involves hands on activities such as laboratory testing, sampling of incoming materials, shipment of samples, inspection of samples and visual inspection of finished goods. | 10/27/2023 |
| 3836 | Berkshire Sterile Manufacturing Lee, MA QA Specialist Bachelor’s degree in scientific discipline, preferred. Exp: 1+ years |
Under general direction, the QA Specialist I is a quality professional who manages quality activities at BSM to meet cGMP and regulatory requirements at BSM. The QA Specialist I is responsible for maintaining and improving the Quality Culture at BSM. | 10/27/2023 |
| 3837 | Vor Biopharma Cambridge, MA Manufacturing Specialist I/II BS or MS in Biology, Biochemistry, Engineering, or related field. Exp: 1 - 5 years |
Vor Bio is seeking a Manufacturing Specialist I/II who is an enthusiastic and driven individual for cGMP manufacturing for early phase cell therapy manufacturing facility. The candidate will be responsible for providing support and executing in the manufacturing of Vor’s gene-edited cell therapies and maintaining compliance of cGMPs in manufacturing areas. | 10/16/2023 |
| 3838 | Voyager Therapeutics Cambridge, MA Sr. Research Associate, Vector Genome Master’s degree. Exp: 1-2 years |
Job Summary: Voyager Therapeutics seeks a highly motivated and experienced protein biochemist to contribute to its research team at its facility in Cambridge, Massachusetts. This is an ideal position for an individual with a background in protein biochemistry, who has a can-do attitude and strong work ethic, and thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. As a Senior Research Associate on the team, you will be responsible for experimental execution and data analysis of various biophysical and biochemical assays to support pipeline programs and new research initiatives. | 10/16/2023 |
| 3839 | Walden Biosciences Cambridge, MA Associate/Research Associate, Cell Systems MS in molecular or cellular biology, or related field. Exp: 0+ years |
As an integral member of our Cell Systems team, the Associate/Research Associate will carry out laboratory research, working collaboratively with the Head of Cell Systems and other members of the Walden Team. This role will contribute to building out the group’s technical capabilities while concurrently undertaking experiments that further our drug discovery programs in vitro and in vivo translational models. | 10/16/2023 |
| 3840 | Zymo Research Tustin, CA Research Associate I BS or MS in Biology, Molecular Biology, Biochemistry, Genetics, or related field. Exp: 1+ years |
We are seeking a highly motivated and proactive individual to join our team for development of next-generation sequencing products as a Research Associate I. The successful candidate will work side by side with some of the most talented people in biotechnology across multiple teams and collaborative partners and will participate in independent product research efforts targeting the development of novel NGS workflows and reagents. The applicant will leverage their skills and familiarity with a range of molecular biology assays, as well as data analysis expertise, to efficiently manage a scientific research project and communicate and interpret data results effectively. The successful candidate will also be a quick learner, have a strong interest in science, and be passionate about a career in research. This position is a full-time and fully onsite role based in our Zymo Research facility in Tustin, CA. | 10/18/2023 |
| 3841 | Zymo Research Irvine, CA Bioinformatics Associate I Holds a master’s or bachelor's degree in Biology, Bioinformatics, Computer Science, Mathematics, Statistics, or a related discipline. Experience may s Exp: 1+ years |
Zymo Research is seeking a highly motivated individual to join our Microbiomics team! The qualified individual will play a key role in developing analysis pipelines for microbiome Next-Generation Sequencing data and performing cutting-edge data science to support Zymo Research’s global product strategy. As part of the Microbiomics team, you will leverage your skills and familiarity with NGS-based microbial sequencing methods in the research and development of new data analysis pipelines for our services, applications and exciting research projects! This position is fully onsite, full-time and is based at the Zymo Research Headquarters in Irvine, CA. | 10/18/2023 |
| 3842 | Zymo Research Irvine, CA Laboratory Technician Bachelor’s degree in Biology, Molecular Biology, Genetics, Microbiology, Biochemistry or related field is a plus. Exp: 1+ years |
Zymo Research is a leading biotechnology company committed to advancing genomics research and personalized medicine. We operate a state-of-the-art Next-Generation Sequencing (NGS) Service Lab, and we are currently seeking a dedicated and detail-oriented Laboratory Technician to join our dynamic team. As a Laboratory Technician in our NGS Service Lab, you will play a pivotal role in ensuring the seamless processing of samples, accurate nucleic acid isolation, precise library preparation, and efficient sequencing of genomic material. Your responsibilities will encompass a range of laboratory tasks, all critical to delivering high-quality results to our clients. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! This position is full – time, fully onsite and is based in the Zymo Research HQ location. | 10/18/2023 |
| 3843 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology Exp: 0-3 years |
JOB DESCRIPTION: The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. | 10/19/2023 |
| 3844 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 10/20/2023 |
| 3845 | Sciecure Pharma Monmouth Junction, NJ Quality Assurance/Document Control Bachelor's degree in science or equivalent is required. Exp: Entry level |
Quality Assurance / Document Control position available at Sciecure Pharma Inc. We are seeking an entry level or partially experienced QA Associate on a permanent basis. Considering local candidates with GMP experience in a manufacturing setting within the QA department. | 10/20/2023 |
| 3846 | Sciecure Pharma Monmouth Junction, NJ Project Coordinator Bachelor’s degree in Life Science (Biology, Chemistry, Chemical Engineering, Etc.). Exp: 1 – 3 years |
Sciecure Pharma Inc. specializes in the research and development of pharmaceutical finished products from conception to commercial. Our growing company is seeking to hire a project coordinator who will be in charge of assisting in organizing our ongoing projects. This task involves monitoring project plans, schedules, organizing and participating in stakeholder meetings, and ensuring that project deadlines are met in a timely manner. To be successful as a project coordinator, you will need to be able to work on tight deadlines, be competent in using Microsoft Office applications such as Word and Excel, and have exceptional verbal, written, and presentation skills. A bachelor’s degree in life science is required for consideration. | 10/20/2023 |
| 3847 | AGC Biologics Boulder, CO Manufacturing Associate I-III BS in Chemistry, Biology or other relevant discipline. Exp: 1-7 years |
The Manufacturing Associate I-III performs GMP manufacturing operations safely, reliably and in compliance with stated processes. We offer a dynamic environment, innovation, operational excellence, and career growth. | 10/20/2023 |
| 3848 | AGC Biologics Seattle, WA QA Associate I-II, In Plant Operations BS degree in Biology, Chemistry or other relevant discipline preferred. Exp: QAAI: 0 - 2 years |
The QA Associate I-II, In Plant Operations is responsible for providing (24/7/365) Quality support to the activities listed below at the Bothell, WA site. Six (6) work shifts are active at the Bothell site: · This position will fill the night shift Wednesday-Saturday 2000-0630 | 10/20/2023 |
| 3849 | AKESOgen Peachtree Crossings, GA Clinical Lab Associate I - Accessioning Bachelor's Degree in a related field preferred. Exp: 0 or more years |
We are looking for a Clinical Lab Associate who will be responsible for Accessioning samples into our Laboratory Information Management System. | 10/20/2023 |
| 3850 | AKESOgen Peachtree Crossings, GA Molecular Technologist I-IV BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 0-2 years |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. | 10/20/2023 |
| 3851 | AKESOgen Chicago, IL Molecular Technologist BS/MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. | 10/20/2023 |
| 3852 | AKESOgen Chicago, IL Molecular Technologist I BS/MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. | 10/20/2023 |
| 3853 | Apton Biosystems Menlo Park, CA Scientist, Research Associate (Molecular) Bachelor's degree in Molecular Biology, Biochemistry or related field. Exp: 1 year |
Pacific Biosciences is looking for a Scientist, Research Associate (Molecular) who will serve as part of the product development team, contributing to the development of Single Molecule Sequencing products for the company’s real-time sequencing platforms. | 10/20/2023 |
| 3854 | Avidity Biosciences San Diego, CA Research Associate, Chemistry BS or MS in chemistry, biochemistry, chemical engineering, or related discipline. Exp: 0 – 3 years |
We are seeking a Research Associate, synthetic chemistry to join our team in La Jolla. This is a hands-on position with responsibility for the design, synthesis, and analysis of organic compounds. The ideal candidate will have biotech/pharma experience in aspects of medicinal chemistry, automated synthesis, and high throughput assay execution. The candidate is expected to be a strong team player, who enjoys scientific discovery and can communicate and collaborate in an interdisciplinary environment. | 10/20/2023 |
| 3855 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline. Exp: 1 to 6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 10/20/2023 |
| 3856 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry. Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 10/20/2023 |
| 3857 | CRISPR Therapeutics San Francisco, CA Research Associate II, CRISPR-X MS in biology or related disciple. Exp: 0-2 years |
We are seeking a Research Associate II to join the CRISPR X group at CRISPR Therapeutics, the leading gene editing company. The successful candidate will be an integral part of a team whose aim is to advance next generation gene editing. The position requires enthusiasm, passion, attention to detail and a desire to assist in developing the next generation of gene editing. | 10/20/2023 |
| 3858 | IDbyDNA San Diego, CA Scientist 1 Scientist 1 Bachelor’s degree. Exp: 0-2 years |
Position Responsibilities: · Executes planned experiments/analysis of moderate to advanced complexity within immediate team and performs routine chemical and biochemical testing; uses insights to help troubleshoot problems · Contributes ideas for meeting project goals and invention disclosures · Assembles data for analysis using accepted methods and distills key conclusions while keeping an organized laboratory notebook and implementing protocols · Provides supporting data to Project Lead on risks in area of responsibility · Understands internal customers and collaborators and their needs and expectations · May train internal customers in areas of expertise Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs. | 10/20/2023 |
| 3859 | IDbyDNA San Diego, CA Engineer 1 - Mechanical Design (R&D/Precision Motion) BSc/MS in ME, EE, Mechatronics, Robotics OR related background. Exp: 0-2+ years |
Responsibilities: Design and test of high precision motion stages Successfully transition designs from concept to production Assist in test development, including nanometer level metrology Analyze designs for vibration and optimal performance and stability Work on teams to perform root cause analysis and methodically solve problems Communicate clearly with team members and leaders Manage and coordinate with external suppliers and manufacturers | 10/20/2023 |
| 3860 | Lampire Biological Labs Coopersburg, PA Abattoir Technician College degree a plus. Exp: 1-2 years |
Job Description: The Abattoir Technician is responsible for collecting, processing, and packaging animal blood and/or tissues sourced from abattoirs. This role involves meticulous attention to detail, adherence to safety and quality standards, and the ability to work at both our laboratory and off-site abattoir/vendor locations as necessary to meet production needs. | 10/20/2023 |
| 3861 | Lampire Biological Labs Pipersville, PA Laboratory Animal Technician Bachelor's Degree in a scientific field preferred. Exp: 0-2 years |
Scope of Responsibility: The project related functions for the small lab animals, including but not limited to mice, rats, guinea pigs, and hamsters. This person will be responsible for preparing and administering injections, performing bleeds, processing bleeds and updating records as needed. To perform animal procedures as the project dictates on small laboratory animals and input data at Lampire with the goal of providing consistent, high quality products and services to our customers with complete, accurate documentation. | 10/20/2023 |
| 3862 | Pharma Tech Industries Royston, GA Quality Control Analytical Chemist I BS degree in Chemistry or BS degree in Biology. Exp: 0-3 years’ |
Pharma Tech Industries (PTI Royston, LLC) is seeking to hire a Quality Control Analytical Chemist I for the Royston, GA facility. Primary responsibilities include performing all duties necessary as a QC Analytical Chemist under the general direction of the department supervisor. This position will report directly to the Quality Laboratory Manager. | 10/20/2023 |
| 3863 | PL Developments Lynwood, CA Chemist III BS in Chemistry / Biochemistry. Exp: 1+ years |
Perform analysis in the functional areas of analytical testing using modern analytical equipment such as HPLC, FTIR, UV, GC, ICP, as well as Wet Chemistry using titration techniques. Provide analytical testing in support of production, analyzes Raw Material, In-Process, Finished product, Stability samples and investigation samples and analyzes and interprets the test data and document result in a timely manner. Thorough understanding and compliance with FDA cGMPs / cGLPs / USP / ICH / SOPs / Test Methods and other recognized standards. Support and be the lead in Analytical and Chemical test method development and test method validations. Writing of SOPs, test methods, study protocols, reports and reviews. Training of lab analysts on analytical test method procedures and usage of equipment and documentation. | 10/20/2023 |
| 3864 | Physical Sciences Andover , MA Optical Engineer Bachelor’s degree in optical or mechanical engineering, physics or equivalent. Exp: 1+ years |
Physical Sciences Inc., a 100% Employee-Owned company located just north of Boston in Andover, seeks an Optical Engineer with professional experience to support development of emerging optical technologies. The candidate will support optical systems design, construction, and testing needs for illuminators, projectors, integrated spectrometers and/or metasurfaces. | 10/20/2023 |
| 3865 | Physical Sciences Andover , MA Experimental Physicist Bachelor or Masters degree in Physics, Applied Physics, Optics, or Related Discipline. Exp: entry level |
Physical Sciences Inc., located just north of Boston in Andover, MA, seeks an experimental physicist with experience in laser-based tools related to applications such as atom sensing, integrated photonics, or optical materials development. The candidate will join teams at PSI and contribute to invention, demonstration, and deployment of technology platforms targeting these application areas. The ideal candidate will have a bachelor’s or master’s degree in physics or related disciplines and should be interested in applied research and development with strong experimental, hardware, and leadership skills. | 10/20/2023 |
| 3866 | Physical Sciences Andover , MA Chemical Engineer Bachelor’s degree in chemical engineering or chemistry is required. Exp: 1+ years |
Physical Sciences Inc. is seeking a chemical engineer to join a multidisciplinary team of engineers and scientists driving innovation in the fields of energy, material science, and aerospace and defense. This individual will play a key role in growing a diverse portfolio of technologies funded by the DoD, DoE, and NASA. The applicant will assist with developing and scaling-up materials production from laboratory/batch processes to pilot-scale/continuous processes. Candidates should have a strong background in reaction kinetics, heat and mass transfer, separations, wet chemistry, and analytical instrumentation. | 10/20/2023 |
| 3867 | Physical Sciences Boston, MA Radio Frequency and Directed Energy Engineer Bachelor’s degree in Electrical Engineering, Physics, or a similar field required. Exp: Recent Graduates |
PSI currently seeks an individual with strong educational and profession experience in RF system engineering, manufacturing, and testing. A solid understanding of theoretical concepts and first principals is a must, as well as the ability to work independently. The ideal candidate will be multi-disciplinary, with strong abilities in systems engineering. This individual will be expected to interact across all engineering disciplines (RF, electrical, mechanical, manufacturing etc.) and develop technology at all stages of development (early stage research TRL 5-10 late stage development). | 10/20/2023 |
| 3868 | Physical Sciences Boston, MA Mechanical Engineer/R&D Entry level candidate with B.S. (or greater) in Mechanical Engineering. Exp: Entry Level |
Physical Sciences Inc., located just north of Boston in Andover, seeks an entry-level to mid-level engineer (B.S. in Mechanical Engineering or similar) to support R&D projects for advanced laser-based sensor systems. This Engineer will be a part of a multi-disciplinary team focused largely on the development and transition-to-production of optical sensing technologies used in environmental and industrial applications (e.g. greenhouse gas emissions reduction, process fluids sensors, standoff or airborne sensors). Recently, sensors developed and deployed include laser-based systems for the detection and quantification of ambient trace gases, or characterization of fuel streams, for the energy industry. | 10/20/2023 |
| 3869 | The Ritedose Corporation Columbia, SC Chemist I BS degree in Chemistry or related field. Exp: 1+ years |
The Chemist I is responsible for performing all the analytical testing related to raw materials, compounding activities, and final product testing including HPLC analysis in the Chemistry laboratory. Other responsibilities include sampling, testing, and releasing of utilities. - Tier 1 Products - Wet Chemistry - HPLC Beginner - GC Beginner | 10/20/2023 |
| 3870 | The Ritedose Corporation Columbia, SC Microbiologist I BS degree or 2 year technical degree in Microbiology or related field. Exp: 0 - 6 months |
The Microbiologist I is responsible for all duties related to performing environmental monitoring, personnel monitoring, microbial enumeration, microbial identification, and sampling of utilities. The Microbiologist I is also responsible for performing all the microbiological testing related to raw materials, utilities, and in-process product testing. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. Level 1 - Less than 6 months experience or no experience - Environmental Monitoring Completion - Utilities completion - Microbial Identification (subculture, Gram-stain, ID entry, VITEK MS assist) - Raw Material Testing including APIs | 10/20/2023 |
| 3871 | Surmodics Eden Prarie, MN Associate Quality Scientist B.S. or B.A. degree in chemistry, biology or appropriate discipline. Exp: 1 year |
The Associate QC Scientist is responsible for testing of raw materials, intermediates, and final products. Testing may be conducted for product release, stability testing, validation, and other purposes. This includes sample preparation, testing and data analysis according to established procedures. The Associate QC Scientist may also perform routine instrument repair and calibration. | 10/20/2023 |
| 3872 | uniQure Lexington, MA QA Specialist I Bachelor’s degree in Life Sciences or Engineering. Exp: 1-3 years |
The Quality Assurance Specialist I, supports the day-to-day quality operations via Manufacturing Clean Room presence, Material/Inventory QA Release, oversight of all elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), investigations, change control, batch review, data integrity, and training in support of biologics manufacturing production. | 10/20/2023 |
| 3873 | uniQure Lexington, MA QC Sample Management Analyst Bachelor’s degree in Life Sciences or Engineering. Exp: 0-1 years |
The Quality Control (QC) Sample Management Analyst supports the day-to-day quality operations within the cGMP QC laboratories via oversight of all elements of sample management including but not limited to receiving, processing, storing, and retrieving all samples appropriately and promptly. This position supports the second shift at uniQure’s state of the art facility in Lexington, MA. | 10/20/2023 |
| 3874 | Acceleron Pharma Rahway, NJ Associate Scientist B.S. or M.S. degree in Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences or related discipline (expected no later than August 2024 Exp: 1+ years |
The successful candidate will be a passionate Scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible for supporting the formulation development of new chemical entities as part of a matrix team from initial first in human formulations (suspensions, solutions, capsules, tablets) through final market formulation definition and manufacturing process robustness assessment. | 10/20/2023 |
| 3875 | Acceleron Pharma Rahway & Kenilworth, NJ Associate Scientist, Biologics Process Research & Development BS (or expected completion by May 2024) in Chemical/Biochemical/Biomedical Engineering, Biotechnology, Biochemistry, Microbiology, Structural biology, Exp: 1+ years |
As an Associate Scientist in BPR&D you will work with a highly collaborative team of scientists and engineers to design, develop and execute robust processes in support of early- to late-stage biological products. You will apply rigorous scientific principles to solve challenging problems focused on developing the best processes to deliver life-changing medicines to patients worldwide. You will also have an opportunity to contribute to additional areas of interest such as biophysical, process, economic and/or multivariate modeling as we are committed to leveraging digital ways of working to enhance our ability to design robust processes. | 10/20/2023 |
| 3876 | Acceleron Pharma West Point, PA Associate Scientist, Upstream Vaccine Process Development Must hold (or plan to complete by December 2023) a BS in Relevant Fields: Chemical Engineering, Biomedical Engineering, Biological Engineering, Bioeng Exp: 1+ years |
Applications are sought for a scientific opportunity in our Company's Vaccines Process Research and Development division. Under the direction of the group leader, this position will be responsible for the upstream process development of vaccine candidates. The successful candidate will perform lab-scale process development/scale-up studies, and develop robust, efficient, scalable cell culture processes for vaccine production. Duties may include: lab-scale fermentation or cell culture, in-process assay support, process scale-up and engineering, maintaining/coordinating raw material and equipment inventories to support development experiments, technology transfer to later stage development groups, and functioning as a key member of an early stage process development team. The incumbent is expected to function in a multi-disciplinary environment and to contribute subject matter expertise to various functional teams engaged in the development of the vaccine candidate. The successful candidate will be expected to demonstrate the ability to convey the results of their work in both verbal and written formats. In addition to the core duties outlined above, the candidate will be expected to keep careful notes, comply with all required training, and maintain focused attention on laboratory safety for themselves and their team. Position requires the employee to be willing to work with infectious agents and/or pathogens. Travel may be needed to support technology transfer. This position will require occasional off-hour and weekend work. | 10/20/2023 |
| 3877 | Santa Cruz Biotechnology Paso Robles, CA Research Assistant Bachelor of Science in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: entry level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. | 10/9/2023 |
| 3878 | Santa Cruz Biotechnology Santa Cruz, CA Research Assistant Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: entry level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Santa Cruz, CA campus. This is a full time position with career advancement opportunities within the company. | 10/9/2023 |
| 3879 | Santa Cruz Biotechnology Ketchum, ID Research Assistant Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: entry level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Ketchum, ID campus. This is a full time position with career advancement opportunities within the company. | 10/9/2023 |
| 3880 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science. Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 10/9/2023 |
| 3881 | SeaGen Everett, WA Quality Control Analyst I - LaunchPad Bachelor's degree in a relevant field. Exp: 0-2 years |
This role performs lab support activities and participates in routine and non-routine testing of environmental samples in cleanroom areas. Completes laboratory work for the support and release of Seagen’s products in a GMP testing environment. Must be able to work weekends, off-shifts, and overtime as required. Applicant must be willing and able to work reliably on a flexible schedule to meet the demands of the project. This position will transition to a shift schedule once qualification activities are complete. | 10/10/2023 |
| 3882 | Sestina Bio Burlingame, CA Research Associate II/III, HTS BS/MS in Biology, Chemistry, Biochemistry or Chemical Engineering Exp: 1-2 years |
We are seeking a Research Associate II/III in our Burlingame location. The candidate will be a part of the high-throughput screening group, with primary responsibility for running screening operations for high-value products made by engineered strains of E. coli, S. cerevisiae, and other microbes. In addition, the candidate will contribute to the development and optimization of new high throughput and microfermentation assays, including automated sample preparation. They will work collaboratively with the rest of the team to optimize strain performance using our GenoScalerTM technology platform in rapid phenotyping of microorganisms. This hands-on position requires a desire and ability to work as a part of a multidisciplinary team, the ability to follow SOPs and run consistent operations, and an interest in continuously developing and improving our ability to characterize production strain through high throughput screening. | 10/10/2023 |
| 3883 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field. Exp: 6 months |
Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 10/10/2023 |
| 3884 | Smithers Wareham, MA Assistant Biologist - Ecotoxicology - Smithers Wareham, MA Bachelors or better in Biology or related field. Exp: 1+ years |
Smithers Environmental Risk Sciences division is seeking an Assistant Biologist in the Ecotoxicology Department at our Wareham, MA location. Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. Incumbent will be introduced to mathematical and statistical procedures used to reduce and analyze study data. Responsible for maintaining cleanliness of the labs, storage and culture areas including maintenance and calibration of equipment used in any of these settings. May require routine involvement in seawater and/or sediment collection. Assignments are completed with minimal supervision. Assists with organization, direction and training of technicians. Assists in coordinating internal requirements for testing (i.e. chemistry support, Quality Assurance, reporting). Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations and company policies.Smithers Environmental Risk Sciences division is seeking an Assistant Biologist in the Ecotoxicology Department at our Wareham, MA location. Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. Incumbent will be introduced to mathematical and statistical procedures used to reduce and analyze study data. Responsible for maintaining cleanliness of the labs, storage and culture areas including maintenance and calibration of equipment used in any of these settings. May require routine involvement in seawater and/or sediment collection. Assignments are completed with minimal supervision. Assists with organization, direction and training of technicians. Assists in coordinating internal requirements for testing (i.e. chemistry support, Quality Assurance, reporting). Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations and company policies. | 10/10/2023 |
| 3885 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field. Exp: 6 months |
Description Job Summary Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. Description Job Summary Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 10/10/2023 |
| 3886 | Smithers West Trenton, NJ Scientist (PCR and Molecular Biology) MS in relevant field Exp: 1-2 years |
Description Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance. PDS works with customers to develop new methods, validate existing methods, and perform the assays necessary to analyze samples from patients on more than 100 clinical trials. PDS is seeking a Scientist with experience in Molecular Biology to join our team. The successful candidate is able to apply prior experience and knowledge to successfully perform in a laboratory environment under regulated conditions. | 10/10/2023 |
| 3887 | Smithers Columbus, OH Associate Chemist I Bachelors or better in Chemistry. Exp: 1+ years |
Essential Functions: Cannabis sample processing of flower, concentrates, extracts, and infused products. Cannabis sample extraction & dilutions. Routine maintenance of laboratory equipment and instrument calibration. Wash glassware used by the laboratory. Accurate entry of sample data into LIMS. Production of laboratory reagents and stocks. Additional duties as assigned. | 10/10/2023 |
| 3888 | Smith & Nephew Columbia, MD Manufacturing Tech I Manufacturing Tech I Manufacturing Tech I Bachelor’s degree in a life science. Exp: 0+ years |
Responsible for hands-on execution of all activities in the manufacturing area including the processing and packaging of human tissue products for transplantation. All duties are performed in compliance with FDA cGMP/cGTP requirements, American Association of Tissue Banks (AATB) standards, and Osiris Therapeutics Inc. standard operating procedures (SOPs). The candidate should have a dedication to high standards of quality. | 10/10/2023 |
| 3889 | Spherotech Lake Forest, IL Manufacturing Associate Bachelor's degree in Chemistry or related field. Exp: 0+ years |
Spherotech, Inc. seeks a college graduate for a Technical Customer Support Representative opening. Duties include, but are not limited to providing customer/technical assistance and Microparticle application support. Responsibilities also include representing the company through trade shows, technical publications, and presentations. Required laboratory skills include: Analysis of Microparticles using particle sizers, flow cytometry, fluorescence spectrophotometry, and microscopy. | 10/10/2023 |
| 3890 | Spherotech Lake Forest, IL Quality Control Associate Bachelor's degree in Chemistry or related field. Exp: 1 year |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. This position requires a Bachelor's degree in Chemistry or related field and a minimum of 1 year of experience. We offer excellent benefits including paid vacation, health insurance, dental insurance, etc. Compensation commensurate with experience. | 10/10/2023 |
| 3891 | StageBio Frederick, MD Laboratory Technician I/II/III College degree preferred. Exp: 0+ years |
StageBio is seeking a full-time Laboratory Technician II to join our Frederick, Maryland facility. | 10/11/2023 |
| 3892 | StageBio Mount Jackson, VA Laboratory Technician I College degree preferred. Exp: 0+ years |
StageBio is seeking a full-time Laboratory Technician I to join our Mount Jackson, Virginia facility. | 10/11/2023 |
| 3893 | Sutro Biopharma South San Francisco, CA Research Associate, Analytical Development BS in analytical chemistry, biochemistry, molecular biology, chemistry, or related scientific field. Exp: 1+ years |
Sutro Biopharma, Inc. is looking for a Research Associate to join our Analytical Development group to support chromatography and mass spectrometry analyses for antibodies (mAb), bispecific antibodies (bsAb), antibody-drug conjugates (ADCs), immunostimulatory antibody-drug conjugate (iADCs) and cytokine derivatives. | 10/12/2023 |
| 3894 | Synlogic Cambridge, MA Quality Control Technician / Senior Quality Control Technician Bachelor’s degree. Exp: 0-2 years |
This is a lab-based role – based in Cambridge MA. Position reports to the Sr. Manger of Quality Control, and will be trained. | 10/12/2023 |
| 3895 | Takeda Boston, MA Research Associate II MS in Molecular Biology, Biochemistry, or Immunology (or equivalent). Exp: 0+ years |
Join Takeda as a Research Associate II where you will produce therapeutics in the areas of oncology, neuroscience and gastro intestinal diseases. You will also implement innovative ideas for cloning bi/multi-specific biologics designs to drive selection of leads and assist the group in implementing new automation technologies. As part of the Global Biologics Research, you will report to High Throughput Protein Production Research Scientist II, Global Biologics. | 10/12/2023 |
| 3896 | Takeda San Diego, CA Research Associate I, GI DDU BS degree in a scientific discipline, or equivalent. Exp: 0+ years |
Join Takeda as a Research Associate I where you will perform Molecular Biology techniques like RNA isolation and qRTPCR as well as in vitro assays (Luminescence-based and Meso scale ELISA). You will also support ongoing and future cell culture experiments to support drug discovery projects for liver disease and will work in an animal related research environment, record keeping of data, and inventory of sample and cell banks. As part of the, Liver Research team you will report to the Scientist II and work with Gastroenterology Drug Discover Unit (GI DDU). | 10/12/2023 |
| 3897 | Takeda Boston, MA Senior Research Associate I, Global Biologics MS in Biochemistry, Biology or a related field (or equivalent). Exp: 1+ years |
Join Takeda as a Senior Research Associate I where you will support the Therapeutic Generation and Screening (TGS) team of Takeda’s Global Biologics Department with demonstrated skills in molecular biology and automation. You will also work independently to generate DNA constructs to be used for expression/ purification of antibodies/ proteins, cell line generation and chimeric antigen receptors. This position will involve extensive use of automation for molecular cloning and plasmid DNA preparation. As part of the TGS team, you will report to the Principal Scientist and work with the Global Biologics organization. | 10/12/2023 |
| 3898 | Takeda Boston, MA Senior Research Associate, CMC Analytical Master’s degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science. Exp: 0+ years |
Join Takeda as a Senior Research Associate, CMC Analytical where you will you will be empowered to develop, validate and transfer analytical methods to advance Takeda`s portfolio. You will also execute basic/routine experiments under limited supervision, plan basic experiments, and perform specialized/complex experiments with assistance from supervisor as appropriate. As part of the Analytical Development team, you will report to Sr Scientist, CMC. | 10/12/2023 |
| 3899 | Takeda Cambridge, MA Senior Research Associate/Engineer III Master degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science. Exp: 0+ years |
You will be a part of the Synthetic Molecule Process Development team. SMPD is responsible for the development of robust, sustainable, and cost-effective processes for the manufacture of new synthetic molecule pharmaceuticals, along with methods for achieving and controlling high standards of purity and quality. As part of the team, you will seek to discover innovative solutions to manufacturing challenges. | 10/12/2023 |
| 3900 | Takeda Boston, MA Senior Research Associate I, In vitro Antibody Discovery MS in scientific discipline. Exp: 1+ years |
Join Takeda as a Senior Research Associate I where you will contribute to discovery of biologics using in vitro (phage) display approaches within the biotherapeutic generation and engineering group, using state-of-the-art discovery technology and creating novel treatments to positively impact patients’ lives in the fields of Oncology, Gastroenterology and Neuroscience. You will also contribute to discovery and engineering of therapeutic biologics including antibodies, sdAb and alternative formats through end-to-end process management, from vector design and library construction, to selection campaigns and screening. As part of the ,Biotherapeutic Engineering team you will report to the Senior Scientist and work with the Global Biologics organization. | 10/12/2023 |
| 3901 | Takeda Boston, MA Cell Therapy Processing Specialist/Senior Specialist Senior Cell Therapy Processing Specialist: Masters degree in chemistry, biotechnology, biology, engineering or related pharmaceutical science. Cell Th Exp: Senior Cell Therapy Processing Specialist: 1+ years; Cell Therapy Processing Specialist: BS: 1+ years; MS: 0+ years. |
The primary focus of the Cell Processing Specialist role will be cGMP cell therapy manufacturing at Takeda’s new cell processing facility in Cambridge, Massachusetts. This position will directly contribute to the successful delivery of novel cell products in support of human clinical trials. | 10/12/2023 |
| 3902 | Tapemark West Caldwell , NJ Equipment Reliability & Process Engineer (1st Shift) Bachelor’s degree in Engineering, Mechanical or Industrial Engineering Exp: 1 year |
Basic Office Setting – Exposure to Computer Monitor Ability to lift or move 25-49 pounds Occasional Travel Ability to Gown for Manufacturing I will abide by all cGMP, FDA and DEA regulatory standards Embrace safety as a value taking responsibility for the safety of themselves and their co-workers Work collaboratively with Production Manager and Director of Production to implement and sustain TPM system practices and culture Create training material and train operators and fabrication leadership on TPM systems and practices. Collaborate with production managers, engineering, and machine operators in the creation of troubleshooting guides, corrective maintenance guides and preventive maintenance procedures. Participate in daily management meetings to report and track equipment reliability metrics like OEE, MTTF & MTBF. | 10/12/2023 |
| 3903 | Tapemark West Caldwell , NJ Process Development Engineer (1st Shift) BS degree chemical or mechanical engineering or related field. Exp: 0-3 years |
Basic Office Setting – Exposure to Computer Monitor Physical Requirements – Not Applicable Occasional Travel Business Dress plus ability to Gown for Manufacturing I will abide by all cGMP, FDA and DEA regulatory standards Under supervision of senior associate, plan and execute process studies for feasibility, development/characterization (Design Of Experiments), and qualification of new products. Recommend changes to process conditions for product quality, throughput, and yield. Write master batch records, protocols, Standard Operating Procedures, process development reports, etc. Analyze data and assist in solving technical problems. Support Validation group with Failure Mode and Effects Analysis (FMEA) and Risk Assessments as needed. Maintain accurate and complete records of development activities in accordance with cGMP guidelines. | 10/12/2023 |
| 3904 | Terumo Cardiovascular Systems Elkton, MD Engineer I, Engineering Rotational Program Bachelor level or higher degree in an engineering discipline from an accredited university or college. Exp: Entry level |
The Rotational Engineer I – Engineering position is an entry level developmental engineering position for establishing a career progression in process, automation/machine and manufacturing engineering through the completion of a 3-year guided program consisting of sequential 1-year assignments in Process Engineering, Automation & Equipment Engineering, and Manufacturing Engineering under the mentorship of senior engineering leaders in each function. Within each assignment, the Rotational Engineer I – Engineering position will support on-going engineering activities by acquiring foundational engineering development skills necessary for the introduction and operation of new processes and equipment for the manufacture of cardiovascular interventional systems products. Key activities may include process design, specification and fabrication of equipment, process validation, process transfer into manufacturing, and continuous improvement and support of full scale production lines. At the successful completion of the 3-year rotational assignment, eligibility for promotion to the Engineer II will be attained. | 10/12/2023 |
| 3905 | Tessera Therapeutics Somerville, MA Research Associate II/Senior Research Associate, LNP Formulation MS in Chemistry, Chemical Engineering, Bioengineering, Pharmaceutical Sciences or related discipline. Exp: 0-3+ years |
Tessera Therapeutics is seeking a Research Associate II/Senior Research Associate, LNP Formulation to develop novel formulation processes to produce lipid nanoparticle (LNP) to support company’s in vitro and in vivo pre-clinical studies. In addition, the successful candidate will develop new techniques to characterize LNP batches. The ideal candidate will be proactive, enthusiastic, and show a passion for process development and formulation. The applicant should have strong communication and collaboration skills, along with a strong background in formulation process development and in LNP characterization. | 10/12/2023 |
| 3906 | Tris Pharma Monmouth Junction, NJ QC Analytical Chemist I Chemist I - Bachelors degree in Chemistry or related science field. Exp: 1-5 years |
The Quality Control (QC) Analytical Chemist I perform analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), stability samples (ST), analytical method transfers and method verifications following analytical methods, United States Pharmacopeia (USP)/National Formulary Chapters, protocols, Standard Operating Procedures (SOPs) under current Good Manufacturing Practices (cGMPs) and company policies. Collaborating closely with, and under the direct supervision of Senior QC Analytical Chemists, Team Leads and QC Managers, the incumbent develops advanced analytical knowledge and expertise while carrying out laboratory work to support QC activities and performs special projects, as assigned | 10/13/2023 |
| 3907 | Tris Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field. Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. | 10/13/2023 |
| 3908 | Turn Biotechnologies Mountain View, CA Research Associate / Sr. Research Associate - Biology BS/MS in biology, biochemistry, molecular biology, or related discipline. Exp: one year |
Turn Biotechnologies is currently seeking a qualified, highly motivated individual for the position of Sr. Research Associate - Biology. This person will be a highly motivated and responsible individual whose primary purpose is to perform and assist with experiments, analyze data, maintain records, manage projects, maintain lab operations, and other duties as required to meet company goals. | 10/13/2023 |
| 3909 | United Therapeutics Manchester, NH Research Associate I/II - Tissue Systems Master’s Degree in cell biology, biomedical engineering or related field. Exp: (RA2) MS: 0+ years |
The Organ Manufacturing group (OMG) at Lung Biotechnology focuses on identifying, scoping, and delivering projects in support of our mission to build cutting edge technology for organ scaffold 3D bioprinting to address the unmet needs for transplantable organs. The Research Associate II-Tissue Systems will work with the direct supervisor to establish new experimental procedures and analytical metrics to characterize the biological outcomes of different lung cell types on 3D printed lung scaffolds. | 10/13/2023 |
| 3910 | United Therapeutics Manchester, NH Research Associate I/II- Tissue Systems Master’s Degree in cell biology, biomedical engineering or related field. Exp: (RA2) MS: 0+ years |
The Organ Manufacturing group (OMG) at Lung Biotechnology focuses on identifying, scoping, and delivering projects in support of our mission to build cutting edge technology for organ scaffold 3D bioprinting to address the unmet needs for transplantable organs. The Research Associate II-Tissue Systems will work with the direct supervisor to establish new experimental procedures and analytical metrics to characterize the biological outcomes of different lung cell types on 3D printed lung scaffolds. | 10/13/2023 |
| 3911 | United Therapeutics Silver Spring, MD Manufacturing Associate I - Fill Finish (1st Shift) Bachelor’s Degree in Arts/Sciences (BA/BS) in a scientific discipline or related field Exp: 1+ years |
The Manufacturing Associate I, Fill Finish provides process support for the production of drug products under strict adherence to cGMP, OSHA, and United Therapeutics policies and regulations in the Silver Spring, Maryland facility. | 10/13/2023 |
| 3912 | United Therapeutics Manchester, NH Research Associate I/II - Cell Production & Process Development Master’s Degree in cellular biology, developmental biology, biomedical engineering or related field. Exp: 0+ years |
The Research Associate II – Cell production and Process Development will perform and contribute to the design of cell studies as well as execute analytical methods to support the production and process development of iPS-derived cells and cellularized 3D scaffolds for the development of autologous 3D printed tissue engineered organs. | 10/13/2023 |
| 3913 | Verge Genomics South San Francisco, CA Research Associate - Neurodegenerative Disease Modeling MS preferably in neuroscience or cell-molecular biology, or a related scientific discipline. Exp: 0- 3 years |
The Target Validation and Exploratory Biology department is seeking a creative and driven research associate to develop state-of-the-art in vitro models representing neurodegenerative disorders using stem cell technology, organoids, 3D co-cultures and microfluidics. With your expertise in genome and stem cell engineering technologies, you will generate different brain cell-types and introduce disease mutations, pathway reporters, and drug target constructs. The candidate will profile quality, functionality and disease relevance of the in vitro brain models through imaging, single cell RNAseq, spatial transcriptomics, proteomics etc. You will benchmark the in vitro models by validating targets identified by Verge Genomics computational platform. This position plays a central role in the Verge Genomics pipeline, intersecting with target validation and drug discovery groups in advancing our pipeline of small molecules and biologics. | 10/13/2023 |
| 3914 | Vero Biotech Atlanta, GA Process Development Engineer Prefer master’s degree in Chemical Engineering. Exp: 1+ years’ |
The mission of this position is to extend the capacity of Vero technical operations group to achieve our strategic objectives, including timely product introductions and overall revenue targets. This role will need to effectively work with the VERO N2O4 Operations, Research & Development, Quality, Regulatory, and Supply Chain teams. Key Performance Indicators for this position include attainment of Throughput, Cost of Goods, Product Quality, Inventory targets, and On-time Delivery goals. | 10/13/2023 |
| 3915 | Vesigen Therapeutics Cambridge, MA Research Associate, Tissue Culture Core (Upstream PD) Bachelor’s or Associate’s degree in biology or related discipline. Exp: 1-3 years |
Vesigen is seeking a creative and highly motivated Research Associate to join our team and help advance the development of the company’s exciting ARMMs technology. The candidate will be an integral member of the R&D team, with opportunities to learn and contribute and develop numerous preclinical programs across several therapeutic areas. | 10/13/2023 |
| 3916 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to help confirm mailing addresses in our directory. Mostly Googling. Can do work any time, any place. Must be able to accept payment via PayPal or Venmo. If interested, send a message through the contact form. Thanks! | 10/6/2023 |
| 3917 | Protomer Technologies Lebanon, IN Manufacturing Scientist - Lebanon API Manufacturing Master's Degree in STEM Discipline (Chemistry preferred). Exp: 1 year |
The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 10/5/2023 |
| 3918 | Protomer Technologies Indianapolis, IN Chemist- Nucleic Acid Synthesis Bachelor's and/or Master's degree Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 10/5/2023 |
| 3919 | Protomer Technologies Boston, MA Plant Engineer Akouos Master's degree in Chemical, Mechanical, Electrical or industrial Engineering, or related field. Exp: 1 - 3+ years |
Join Akouos, a Lilly company, as a Plant Engineer III, The Plant Engineer III will serve as a Technical Lead for Capital projects, overseeing GMP manufacturing process equipment at the AKOUOS facility in Boston, MA. This individual will collaborate closely with Facilities and Engineering management, and equipment End Users to successfully drive projects to completion. The ideal applicant will thrive in a fast-paced, dynamic, and innovative environment, and will play a critical role in ensuring that projects are executed efficiently and effectively to meet objectives and timelines. Drive results by owning and completing medium to large scale projects with challenging timelines. Ensure appropriate root causes and corrective actions are identified through troubleshooting and investigation processes. | 10/5/2023 |
| 3920 | Protomer Technologies Boston, MA Associate Scientist, Early Preclinical Development Bachelor's Degree Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 10/5/2023 |
| 3921 | Protomer Technologies Boston, MA Upstream Process Development Engineer Master's degree in Biochemistry, Chemical Engineering, Bioengineering or related discipline. Exp: 1-3+ years |
The Process Development group at Akouos is seeking an innovative Engineer to provide hands-on development support for the manufacturing of AAV-based gene therapy vectors. The ideal candidate for this position is an experienced Engineer with a strong background in AAV vector cell culture technologies and an excellent track record in gene therapy upstream process development. The successful candidate will actively participate in upstream process development, scale-up, process optimization, and process tech transfer for GMP manufacturing. The successful candidate will thrive in a collaborative, scientifically stimulating, and fast-pace work environment. | 10/5/2023 |
| 3922 | Protomer Technologies Indianapolis, IN Manufacturing Scientist – API Manufacturing Process Support Master's Degree in STEM Discipline (Chemistry focus preferred). Exp: 1 year |
The Manufacturing Scientist provides the technical support required to achieve the reliable and compliant manufacture of the Active Pharmaceutical Ingredient External Manufacturing (API EM) portfolio which includes raw materials, intermediates, enzymes and bulk drug substances. The API EM Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and technically independent in setting up and executing a variety of experiments at the laboratory scale and conduct research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 10/5/2023 |
| 3923 | Protomer Technologies Branchburg, NJ Research Associate-QC Biochemistry BS or MS in a related science such as a Biology or Biochemistry Exp: 0 - 5 years |
Conduct routine and non-routine analyses of in-process materials, raw materials, environmental/water samples, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. Perform routine QC responsibilities as needed. Apply acceptable cGMP practices during execution of all work tasks. Work independently with moderate supervisory guidance. | 10/5/2023 |
| 3924 | Pyxant Labs Salt Lake City, UT Analyst I Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
Learns to analyze samples for various compounds and components in compliance with SOPs and regulatory agency guidelines. | 10/5/2023 |
| 3925 | Quanterix Billerica, MA Manufacturing Associate I BS in Chemistry, Biology or related Life Sciences Exp: 0+ years |
To continue our extraordinary growth, we are hiring a Manufacturing Associate I located in Billerica, MA. We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 10/5/2023 |
| 3926 | Quanterix Billerica, MA Quality Control Analyst I Bachelor's Degree in Chemistry/Biochemistry/Biology or related field preferred Exp: 1+ years |
To continue our growth, we are hiring a Quality Control Analyst I located in Billerica, MA. This position will be part of our Quality Control team, responsible for a variety of activities including immunoassay testing on automated and semi-automated platforms, advanced data analysis, and prioritization and coordination and new product launch readiness in accordance with cGMP. | 10/5/2023 |
| 3927 | Quanterix Billerica, MA Manufacturing Associate I - 2nd Shift BS in Chemistry, Biology or related Life Sciences Exp: 1+ years |
To continue our extraordinary growth, we are hiring a Manufacturing Associate I located in Billerica, MA. We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 10/5/2023 |
| 3928 | Quanterix Billerica, MA Downstream Manufacturing Associate I BS in Chemistry, Biology or related Life Sciences Exp: 0+ years |
To continue our extraordinary growth, we are hiring a Downstream Manufacturing Associate I located in Billerica, MA. We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 10/5/2023 |
| 3929 | Quidel Athens, OH Protein Biochemist I Bachelor’s Degree in a biology, biochemistry, chemistry or other related science field. Exp: <1-year |
The Protein Biochemist I is responsible for the production of various proteins and their conjugation as well as antigen production and maintenance for downstream manufacturing, finished good catalog items, and custom orders in accordance with Quidel’s Quality System Regulations. This role is located in Athens, Ohio. | 10/5/2023 |
| 3930 | Quidel Carlsbad, CA Associate Process Group Chemist B.S./B.A. Life/Applied Sciences. Exp: 6 months |
As we continue to grow as QuidelOrtho, we are seeking an Associate Process Group Chemist, in accordance with forecasted requirements, participates in the manufacture of products within QSR and ISO regulations. This position reviews and reconciles documents and work orders, supports assigned projects with supervision, participates in product transfers, supports departmental troubleshooting and process improvement teams, and displays an improving working knowledge of business processes as they relate to manufacturing. This role is located in Carlsbad, CA onsite. | 10/5/2023 |
| 3931 | Quidel San Diego, CA Development Associate I BS/BA or equivalent in life sciences or chemistry. Exp: 1-3years |
As we continue to grow as QuidelOrtho, we are seeking a Development Associate I to join our research & new product development team. This person will participate in activities to support research and new product development. The position performs simple experiments as directed by Scientist or Manager. This position is onsite at our Summers Ridge office in San Diego, CA. | 10/5/2023 |
| 3932 | Quidel Athens, OH Associate Molecular Biochemist BA/BS in life sciences or MA/MS in related life sciences field. Exp: BS: 0-2 years; MS: 0 years |
As we continue to grow as QuidelOrtho, we are seeking an Associate Molecular Biochemist. Responsibilities include synthesis and analysis of small to mid-scale purified proteins and oligonucleotides and relevant in-process quality assessment activities, as well as supporting research and new product development utilizing these components (flex studies etc.). Responsibilities may include GMP protein/oligonucleotide analysis and providing support in addressing issues that may cause product supply interruptions. This role is also responsible for all in-process production activities for molecular assays. This position requires a high level of technical acumen, attention to detail and on the job training to become proficient across the multifaceted production spectrum required for advanced molecular production. This includes proficiency with autonomous production and ISO 13458/IVDR/510K quality requirements for over 500 molecular SKUs, specific handling of highly specialized equipment, proficiency in cGMP manufacturing techniques under Quidel’s Quality System. This position is located in Athens, Ohio | 10/5/2023 |
| 3933 | QuVA Pharma Bloomsbury, NJ Chemist 2nd Shift B.S. or M.S. degree in chemistry, biology or related field. Exp: 0- 2 years |
Responsibilities may include: Reads and understands SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements Provide analytical data in a timely manner. This includes understanding of Supervisor or Manager’s expectations Provide input to R&D SOPs to enhance the efficiency of the laboratory Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements Communicate as needed any testing issues to either a Supervisor or Manager or to a cross-functional group such as Metrology | 10/5/2023 |
| 3934 | QuVA Pharma Bloomsbury, NJ Microbiologist 1st shift B.S. degree in related field (preferably Microbiology). Exp: 0-2 years |
Responsibilities may include: Compiles and interprets results of environmental monitoring tests and sterility results Conducts investigations of all non-conforming results Identifies environmental microbial isolates by classical techniques and automated identification methods to meet the requirements of the microbial environmental monitoring program Evaluates cleaning effectiveness on a routine basis to determine robustness of disinfection Develops and/or performs water sampling, including DI water, WFI and steam per the program (when needed) Performs and/or oversees surface and air sampling of the facility areas and equipment per the program Performs and/or oversees environmental monitoring of all facility areas in compliance with gowning requirements Validates methods and perform sterility (USP <71>), Scan RDI and endotoxin (USP <85>) testing for finished goods Performs growth promotion testing of media Prepares reports and communicate results for the environmental program per facility standards Trains and maintains current training status on required equipment and procedures Other duties as assigned | 10/5/2023 |
| 3935 | QuVA Pharma Bloomsbury, NJ Chemist 1st Shift B.S. or M.S. degree in chemistry, biology or related field. Exp: 0- 2 years |
Responsibilities may include: Reads and understands SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements Provide analytical data in a timely manner. This includes understanding of Supervisor or Manager’s expectations Provide input to R&D SOPs to enhance the efficiency of the laboratory Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements Communicate as needed any testing issues to either a Supervisor or Manager or to a cross-functional group such as Metrology | 10/5/2023 |
| 3936 | Reata Pharmaceuticals Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred). Exp: Entry Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 10/5/2023 |
| 3937 | Minaris Regenerative Medicine Allendale, NJ QC Analytical Associate I BA/BS in a science or relevant field required. Exp: 1-2 years |
The Quality Control Analytical Associate serves as a support role to clinical and commercial production. The QC Analytical Associate will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. | 10/5/2023 |
| 3938 | Minaris Regenerative Medicine Allendale, NJ QC Analytical Associate I BA/BS in a science or relevant field required. Exp: 1-2 years |
The Quality Control Analytical Associate serves as a support role to clinical and commercial production. The QC Analytical Associate will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. | 10/5/2023 |
| 3939 | R & D Systems Minneapolis, MN Advanced Research Associate, Cell & Gene Therapy Master’s degree in a related field. Exp: up to 2 years |
This position will work within the Cell and Gene Therapy Applications group to provide scientific support of cell and gene therapy related Bio-Techne products. In this role, you would be responsible for assisting in lab maintenance, performing cell culture experiments, running molecular biology experiments, and writing standard operating procedures. This position is a fantastic opportunity for continuous learning and development in the rapidly evolving cell and gene therapy field. | 10/5/2023 |
| 3940 | R & D Systems Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
We are seeking an Advanced Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 10/5/2023 |
| 3941 | R & D Systems Minneapolis, MN Advanced Manufacturing Technician 4 year science degree. Exp: 1+ years |
The responsibilities of the Advanced Manufacturing Technician are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include filling containers with product, feeding a production machine, labeling product, recording data, operating equipment, formulation, and plate coating. This position offers 1st shift hours of 8:00am-4:30pmThe responsibilities of the Advanced Manufacturing Technician are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include filling containers with product, feeding a production machine, labeling product, recording data, operating equipment, formulation, and plate coating. This position offers 1st shift hours of 8:00am-4:30pm | 10/5/2023 |
| 3942 | R & D Systems Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 years |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 10/5/2023 |
| 3943 | R & D Systems Minneapolis, MN RA - Advanced Research Associate Master’s degree. Exp: minimal experience |
In this role, you would be responsible for the development and execution of QC test method validations for a variety of products, utilizing a wide variety of laboratory techniques. This position also assists in troubleshooting investigations and process improvement projects. As an Advanced Research Associate, you will also participate in cross-functional teams focused on new product introduction. | 10/5/2023 |
| 3944 | R & D Systems Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in Molecular Biology. Exp: 0-2 years |
The responsibilities of this position are to assist the protein product development team in the area of recombinant protein expression. This includes the preparation of eukaryotic expression vectors, cell culture, and screening procedures. The successful candidate will perform various techniques such as DNA preps, sub-cloning, mammalian and insect cell culture, transfections, Western blotting, ELISA, and flow cytometry. They will also prepare buffers and reagents, assist in cleaning and maintenance of the laboratory and equipment, and perform other general lab duties as assigned. | 10/5/2023 |
| 3945 | R & D Systems Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 10/5/2023 |
| 3946 | Roche Seattle, WA Lab Assistant I Bachelor’s degree focused in Biology, Biotechnology, Biochemistry, Chemistry, Physics or Engineering field preferred. Exp: 1+ years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its novel Sequencing by eXpansion (SBX™) technology. SBX™ uses unique applications from chemistry, biochemistry, and protein engineering to sequence DNA by nanopore in rapid time with high accuracy and low cost. You will join the Central Service team and assist in the day-to-day operations of the company. The Central Service team plays an integral role within the company. Members are passionate and dedicated to our SBX™ technology and the impact high throughput, low-cost DNA sequencing will have on patient outcomes. We are looking for individuals who share this passion and are excited to join a dynamic team. Please include a cover letter outlining why you want to work with us, your specific interest in our technology, and how you would contribute. | 10/5/2023 |
| 3947 | SAMDI Tech Chicago, IL Research Assistant B.S. in biology, biochemistry, chemistry, or related field. Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. | 10/6/2023 |
| 3948 | Sangamo Therapeutics Richmond, CA Research Associate (CONTRACT) B.S. or higher in biology, virology, biochemistry, process engineering or related field. Exp: 1+ years |
Sangamo Therapeutics is seeking a talented temporary Research Associate to fill an open position in our Vector Core Production Group. Tasks would include viral vector production using mammalian tissue culture cells and vector purification by ultracentrifugation or column chromatography. Maintenance of our production and inventory database is also required. Analysis of the viral vectors by qPCR and gels may also be performed. The position requires adaptability, excellent planning and communication skills as well as the ability to work in a fast-paced, team-oriented, multidisciplinary environment. | 10/6/2023 |
| 3949 | Sangamo Therapeutics Brisbane, CA Research Associate – Bioassay Analytical Development (Contract) BS/MS in Biological Sciences such as Molecular Biology, Immunology, Virology, or related discipline. Exp: 1 year |
We are seeking a highly motivated Research Associate to support the development of our Adeno-associated virus (AAV) gene therapy products and gene-edited cellular therapies. In this role, the candidate will contribute to developing and qualifying a new cellular platform to enable a variety of Sangamo’s cell and gene therapy development programs. This is a laboratory-based position that requires creativity, organization, attention to detail, excellent communication and presentation skills, and a capacity for constant innovation in pursuit of company goals. The ideal candidate will be experienced in using mammalian cells to develop appropriate cell models to support cell-based assays along with a fundamental understanding of ICH guidelines for the method qualification. The environment is exciting, fast-paced and offers the opportunity to work at the cutting edge of cell and gene therapy. | 10/6/2023 |
| 3950 | Sanofi Genzyme Framingham, MA Research Associate, Genomic Medicine Bioanalytics BS in biological sciences or related field. Exp: 1 – 3 years |
The Research Associate is responsible for executing test methods under control of established procedures. Specifically, performing in-process and release testing of cellular therapies out of our 45 NYA manufacturing facility. Additional functions will include interpretation of data, preparation of test documentation, and management of analytical databases. We are looking for a candidate that is capable of learning quickly with the goal of executing analytical methods and managing assigned test schedules, with excellent communication skills. The position is located in Framingham, MA. | 10/6/2023 |
| 3951 | Sanofi Genzyme Framingham, MA Senior Research Associate - Biologics Drug Product Development Master’s degree in biochemistry, pharmaceutical science, chemical or protein engineering, or related field. Exp: 0+ years |
The senior research associate (SRA) will be part of Global Drug Product Development and Manufacturing, supporting biologic drug product formulation and process development. The SRA will play a critical role in supporting laboratory-based studies working on different facets of drug product formulation and process development, across multiple modalities including monoclonal antibodies (mAb), multi-specific antibodies, therapeutic enzymes, and fusion proteins. Formulation work would include both liquid and lyophilized formulation development, and process characterization from early phase 1 through phase 3 drug product development. | 10/6/2023 |
| 3952 | Sanofi Genzyme Waltham, MA Senior Research Associate, Genomic Medicine Unit - BioProcess Analytics Masters degree in biological sciences. Exp: 0+ years |
The BioProcess Analytics group located in Waltham, MA is seeking a highly motivated Senior Research Associate to join our team of talented individuals. The successful candidate must have a basic understanding of analytical method development and technologies, with scientific knowledge in cell and gene therapy analytics preferred. The candidate must be highly motivated, well organized, able to execute studies independently, collaborative, and able to communicate effectively with a cross-functional team. | 10/6/2023 |
| 3953 | Sanofi Genzyme Framingham, MA Senior Research Associate - Cell Line Development Master’s degree in Biology, Cell Biology, Biotechnology or related discipline. Exp: 0+ years |
We are seeking a highly motivated candidate to join a high-performing, collaborative group working on different aspects of CHO cell line development. Responsibilities will focus on generation and evaluation of cell lines producing recombinant biologics, including monoclonal antibodies and other protein formats, and performing experiments to help drive process improvements. Work will directly support development projects in Sanofi’s pipeline. | 10/6/2023 |
| 3954 | Sanofi Genzyme Waltham, MA Research Associate - Cell Culture Process Development - Genomic Medicine Unit Bachelor’s degree in biological science or engineering discipline. Exp: 1+ years |
The Genomic Medicine Unit (GMU) CMC group at Sanofi is dedicated to the establishment of best in class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV vectors and cell therapy products. This organization encompasses vector and cell line engineering, upstream and downstream process development, analytics, and clinical manufacturing support. The cell culture process development group is responsible for viral vector production optimization and development of next generation production platforms to support high dose therapeutic products. The group is seeking a motivated Research Associate to join the team. | 10/6/2023 |
| 3955 | Sanofi Genzyme Framingham, MA Senior Research Associate - QC, Genomic Medicine Bioanalytics - CT Master’s degree in Biology/Biochemistry or related discipline. Exp: 0+ years |
This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi’s CMC Development organization. The GMU Analytical Development group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust analytical methods to support release and characterization testing of different cell therapy candidates. The group supports cGMP-compliant in-process Quality Control (QC) support of cGMP Manufacturing cutting edge methods such as flow cytometry. The selected candidate will execute rapid turnaround cGMP testing of in-process materials. In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month. | 10/6/2023 |
| 3956 | Sarepta Therapeutics Columbus, OH Research Associate I/II, Immunology B.A. or B.S. degree in Biological Sciences or related discipline. Exp: 1-3 years |
Sarepta Therapeutics is seeking a motivated Research Associate I/II (RA I/II) that will perform experiments under the direction of Immunology lab members, collecting and verifying research data as well as performing assays to support clinical and non-clinical trials. The RA I/II will help organize and prepare research materials as well as assist in maintaining equipment, documentation, and inventory. This is a lab-based position that contains occasional weekend and late evening work. | 10/6/2023 |
| 3957 | Omniome Menlo Park, CA Scientist, Research Associate (Molecular) Bachelor's degree in Molecular Biology, Biochemistry or related field. Exp: 1 year |
Pacific Biosciences is looking for a Scientist, Research Associate (Molecular) who will serve as part of the product development team, contributing to the development of Single Molecule Sequencing products for the company’s real-time sequencing platforms. | 9/26/2023 |
| 3958 | Omniome San Diego, CA Engineer II, Systems Integration Masters degree Exp: 1-3 years |
Pacific Biosciences seeks a talented, driven, and experienced system integration engineer to join the System Integration and Verification Team. The candidate will be responsible for integrating and testing all aspects of the system including hardware, software, and consumables. | 9/26/2023 |
| 3959 | OmniSeq Durham, NC Flow Cytometry Analyst Bachelors in Medical Technology or Bachelors in chemical, physical or biological science. Exp: BSMT: 0+ years; BS: 6 months |
$5,000 SIGN ON BONUS FOR EXTERNAL CANDIDATES. We are offering exciting opportunities to join our team as a Flow Cytometry Analyst - Technologist in Research Triangle Park at the Center for Molecular Biology and Pathology, Durham, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". This Analyst will work alongside a highly trained staff with the latest technology. Our services are performed with the utmost care, expertise, integrity and respect for the patient. The work schedule for this position will be Wednesday-Saturday 10:00am-8:30pm, 1st shift. | 9/26/2023 |
| 3960 | OmniSeq Richmond, VA Technologist - Microbiology Associate degree in Medical Lab Science OR Bachelor degree in chemical, physical or biological science. Exp: 6 months |
Are you looking to embark on a new challenge in your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technician OR Technologist in Richmond, VA. In this position you will work in a Microbiology lab. The work schedule for this position will be: 2nd shift Monday-Friday 1pm-9:30pm | 9/26/2023 |
| 3961 | OmniSeq Research Triangle Park, NC ToxAssure Technologist - 1st Shift Bachelor's degree in Biology, Chemistry, Medical Technology or a related life science. Exp: 1 year |
Labcorp is seeking a ToxAssure Technologist or Technologist Trainee to join its team in Research Triangle Park, NC! This position will be working in the ToxAssure lab which performs urine medical drug monitoring testing. This is a great opportunity to join an innovative organization and receive targeted one-on-one training that will help the individual grow their career in the Toxicology Clinical Laboratory industry! The work schedule for this position will be 1st shift - Sunday-Thursday, 7:00 am – 3:30 pm | 9/26/2023 |
| 3962 | OmniSeq Burlington, NC Technologist for Chemistry Bachelor's degree Biology, Chemistry, Medical Technology or related. Exp: 1 year |
$2,500 Sign-On Bonus External Candidates Only! Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist for Chemistry department located in Burlington NC! In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". The schedule for this position will be: 1st shift, Saturday, Sunday, & Monday, 7:00am-7:30pm. | 9/26/2023 |
| 3963 | OmniSeq Greenfield, IN Research Assisatnt I - Cell Based and Immunology Team BS/BA degree in science or related field Exp: 0+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 9/27/2023 |
| 3964 | OmniSeq Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field Exp: 0+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 9/27/2023 |
| 3965 | OmniSeq Greenfield, IN Research Assistant I - Protein Chemistry BS/BA degree in science or related field Exp: 0+ years |
If you have a passion for science and working in a dynamic and fast paced lab with a cohesive team, the Research Assistant position will take you to the next level in your career. We have an excellent opportunity for someone to join our Protein Chemistry team in Greenfield, IN. In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 9/27/2023 |
| 3966 | Pacific Edge Hummelstown, PA Laboratory Technician Bachelor's degree in medical technology, chemical, physical, or biological sciences. Exp: 1 year |
Pacific Edge Diagnostics USA, an innovative cancer detection testing company is seeking a talented Clinical Laboratory Technician to join its team. The Clinical Laboratory Technician's primary responsibility will be to perform molecular clinical testing (from specimen receipt through reporting patient results), as well as general lab maintenance. | 9/28/2023 |
| 3967 | Pacira Biosciences San Diego, CA QA Associate 1 BS/BA degree in scientific discipline from an accredited college or university. Exp: 1 year |
This person is to assist and support the organization with GMP compliance, monitoring conformance to established quality assurance processes and GMP standards for manufacturing. | 9/28/2023 |
| 3968 | Pall New Port Richey, FL Manufacturing Engineer Bachelor of Science degree in Manufacturing, Mechanical, Industrial, and/or Aerospace Engineering or other related engineering field, required. Exp: 1+ years |
The Manufacturing Engineer is responsible for improvements within value streams of responsibility, in line with yearly targets in the areas of Safety, Internal and External Quality, On-Time Delivery / Lead Time reduction, and Productivity. This position is part of the Aerospace machine shop department and will be located onsite (full-time) in New Port Richey, FL. | 9/28/2023 |
| 3969 | Paradigm Diagnostics Marshfield, WI Clinical Laboratory Technician - Rare Disease Sequencing Laboratory Bachelor's degree in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution. Exp: 0+ years |
The Clinical Laboratory Technician is responsible for performing standard laboratory procedures within the assigned department/laboratory. The Clinical Laboratory Technician will analyze data and may assist with research and development. This incumbent will be relied upon to follow laboratory protocols and maintain high quality levels. This role is located onsite in Marshfield, WI and works in our Sequencing Laboratory. The training for this role is 8 weeks Monday-Friday 8am-4:30pm. After training, the shift options are: Rotating 4-day/10-hour shift. Wednesday-Friday/Tuesday 7am-5:30pm with every 3rd weekend, 6:00am-4:30pm. 4-day/10-hour shift. Tuesday-Friday 12:00pm-10:30pm. | 9/28/2023 |
| 3970 | Par Pharmaceutical Horsham, PA Manufacturing Associate II, Downstream Processing BS degree Exp: 1+ years’ |
The Manufacturing Associate II, Downstream Processing works in a hands-on capacity in the cGMP purification and production support areas to manufacture collagenase clostridium histolyticum bulk drug substance (CCH BDS). This role authors and revises manufacturing & process documentation and is responsible for supporting necessary purification and production-related activities, including validation and development work as needed. | 9/28/2023 |
| 3971 | Par Pharmaceutical Horsham, PA Manufacturing Associate II, Upstream Processing BS degree Exp: 1+ years’ |
The Manufacturing Associate II, Upstream Processing works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture collagenase clostridium histolyticum bulk drug substance (CCH BDS). This role authors and revises manufacturing and process equipment documentation and is responsible for supporting necessary fermentation and production activities, including validation and development work as needed. | 9/28/2023 |
| 3972 | Par Pharmaceutical Rochester, MI Chemist II (Weekend Shift) Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years’ |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 9/28/2023 |
| 3973 | Parse Biosciences Seattle, WA Research Associate I - Single Cell Genomics BA or BSc in molecular biology (or related field) Exp: one year |
As a Research Associate at Parse Biosciences, you will work at the cutting edge of molecular biology and genomics as part of a collaborative team. You will design and perform experiments to improve our existing single-cell RNA-sequencing kits as well as demonstrate new applications for our kits. You will also share responsibilities in organizing inventory, assembling kits, testing kits internally, reagent quality control, and maintaining the lab. | 9/28/2023 |
| 3974 | Pharmaron San Diego, CA In Vivo Research Associate I, PK BS Exp: 1-year |
Pharmaron (San Diego) is seeking to hire an outstanding candidate to join our PK department at the Research Associate I level. The Research Associate will play an important role by supporting in vivo pharmacokinetic studies. Primary responsibilities: This position requires a broad knowledge of anatomy, physiology, and biochemistry to help develop and support in vivo models to screen therapeutics and devices being developed for various disorders. Experience with surgical, dosing, and sampling techniques is required | 9/29/2023 |
| 3975 | Pharmaceutics International Hunt Valley, MD Aseptic Manufacturing Technician, Formulation Bachelor’s degree Exp: 1 year |
The Manufacturing Technician is responsible for the implementation of routine production and manufacturing procedures to support processes and ensure compliance with regulatory requirements. The Associate will work with the Drug Product team to ensure the successful completion of various cGMP activities. The Associate will partner in optimizing both technical aspects as well as quality systems which governs cGMP manufacturing. | 9/29/2023 |
| 3976 | Pharmaceutics International Hunt Valley, MD QC Microbiologist I- 2nd Shift B.S / M.S. in a life sciences discipline Exp: 0-2 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions. | 9/29/2023 |
| 3977 | Pharmaceutics International Hunt Valley, MD Manufacturing Equipment Engineer Bachelor of Science in Engineering, mechanical engineering preferred Exp: 1 – 5 years |
The Manufacturing/Equipment Engineer is responsible for aspects of growing and improving the facility and equipment at our development and manufacturing sites. Most of the process will be liquid formulations manufactured under single-use production concept, in cleanroom environment. This role is involved in onboarding new process equipment, working closely on the ground with production and development personnel, organizing the production process equipment layout, and coordinating with other departments to ensure the validated status of process equipment. All work to be carried out in compliance with cGMP and company standard operating procedures and policies. | 9/29/2023 |
| 3978 | Pharmaceutics International Hunt Valley, MD QC Microbiologist I- 3rd Shift B.S / M.S. in a life sciences discipline Exp: 0-2 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions. | 9/29/2023 |
| 3979 | Phitonex Middleton, WI Entry Level Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3980 | Phitonex Middleton, WI Entry Level Chemist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3981 | Phitonex Middleton, WI Entry Level Biochemist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3982 | Phitonex Rockville, MD Lab Technician I Prefers BS in a Biological Science. Exp: 1 yr |
This position is within the Fisher BioServices business unit of Thermo Fisher Scientific. The Laboratory Technician will assist in manual and automated laboratory processing of biological materials, including aliquoting and sample preparation. | 9/29/2023 |
| 3983 | Phitonex Plainville, MA Engineer I, Manufacturing Engineering B.S. degree in mechanical engineering, biochemical engineering, chemical engineering, electrical engineering or related engineering field preferred. Exp: Entry level to 2 years |
The Engineer I, Plant will be vital in supporting the groundbreaking VVS commercial facility in Plainville, MA. This position will play an important operations support role in the site Facilities and Engineering team where they will support manufacturing, laboratory and warehouse operations in Plainville, MA. | 9/29/2023 |
| 3984 | Phitonex Lexington, MA Plant Engineer I Engineering Degree (required) in relevant discipline is strongly preferred (Bachelor of Science degree in electrical, chemical, mechanical, or maritim Exp: 1 year |
Job Description At Viral Vector Services (VVS), a division of Thermo Fisher Scientific, we deliver from process development through commercial supply, we offer the expertise and resources vital to help clients deliver innovative gene therapies. Placed in the forefront of our leading and innovative Cell and Gene Therapy business enabling clients to cure genetic, rare, and otherwise untreatable diseases | 9/29/2023 |
| 3985 | Phitonex Cambridge, MA Process Engineer I, Manufacturing Technical Services - Upstream Bachelor’s degree (required) in biochemical or chemical engineering, pharmaceutical science or a related scientific discipline such as chemistry or bi Exp: 0-2 years |
US - Massachusetts - Cambridge Responsible for the support of clinical and commercial drug manufacturing at the viral vector manufacturing facility located in Cambridge, MA. Scope includes supporting the at-scale manufacture of late-stage and commercial gene therapy drugs from both a process and equipment standpoint with a focus on the upstream process and technology. Individual will join an experienced team of process engineers working closely with groups such as manufacturing, quality assurance, quality control, and validation. | 9/29/2023 |
| 3986 | Plex Pharma San Diego, CA Research Associate, Biology & Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field. Exp: 1-3 years |
Plex Pharmaceuticals (www.plexpharma.com), a biotechnology company with a focus on developing novel drugs targeting misfolded and aggregated proteins, has an immediate opening for a Research Associate. The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 9/29/2023 |
| 3987 | PPD Middleton, WI Associate Scientist - Microbiology - 2nd Shift Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3988 | PPD Middleton, WI Assistant Scientist - Microbiology 2nd Shift Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3989 | PPD Devens, MA Associate Scientist - ELISA, HPLC Bachelor's degree in Biochemistry, Biotechnology, Analytical Chemistry, or equivalent and relevant formal academic / vocational qualification. Exp: 0-2+ years |
You will be responsible for supporting analytical activities within Biologics Process Development (PD). The role will involve supporting in-process analytical testing, delivering results within customer and project timelines, assay harmonization activities within the network groups, and evaluation of new analytical technologies. You will have excellent communication skills, is a team player, and have experience in Bioanalytical techniques as they apply to Biologics and related process impurities. Techniques of interest include Capillary Electrophoresis, Liquid Chromatography, and ELISAs. A reasonable appreciation of upstream and downstream process development activities is highly desirable. The role will provide Analytical support within PD. The candidate will work closely with PDA team members and Process Development to deliver quality analytical data in a timely manner. | 9/29/2023 |
| 3990 | PPD Providence, RI Associate Scientist - Mechanical Testing Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar. Exp: 0 to 1+ years’ |
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. | 9/29/2023 |
| 3991 | Principia Biopharma Waltham, MA Research Associate, Purification Process Development Bachelor’s degree in biological science or engineering discipline. Exp: 1+ years |
The Genomic Medicine Unit (GMU) Chemistry, Manufacturing and Control (CMC) group at Sanofi is dedicated to the establishment of best-in-class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV, non-viral vectors, and cell therapy products. The GMU purification process development group is responsible for the development of AAV processes and for supporting viral vector purification from next-generation production platforms to enable high-dose gene therapy programs. The Research Associate, Purification Process Development role requires leadership both inside and outside the laboratory and will rely on industry expertise and the exploration of novel technologies to build robust and efficient purification processes consistent with patient safety standards. We are looking for a motivated candidate with good communication skills and desire to learn advanced purification methods and contribute to organizational goals. | 9/29/2023 |
| 3992 | Principia Biopharma Framingham, MA Senior Research Associate - Biologics Drug Product Development Master’s degree in biochemistry, pharmaceutical science, chemical or protein engineering, or related field. Exp: 0+ years |
The senior research associate (SRA) will be part of Global Drug Product Development and Manufacturing, supporting biologic drug product formulation and process development. The SRA will play a critical role in supporting laboratory-based studies working on different facets of drug product formulation and process development, across multiple modalities including monoclonal antibodies (mAb), multi-specific antibodies, therapeutic enzymes, and fusion proteins. Formulation work would include both liquid and lyophilized formulation development, and process characterization from early phase 1 through phase 3 drug product development. | 9/29/2023 |
| 3993 | Principia Biopharma Framingham, MA Senior Research Associate - Cell Line Development Master’s degree in Biology, Cell Biology, Biotechnology or related discipline. Exp: 0+ years |
We are seeking a highly motivated candidate to join a high-performing, collaborative group working on different aspects of CHO cell line development. Responsibilities will focus on generation and evaluation of cell lines producing recombinant biologics, including monoclonal antibodies and other protein formats, and performing experiments to help drive process improvements. Work will directly support development projects in Sanofi’s pipeline. | 9/29/2023 |
| 3994 | Principia Biopharma Framingham, MA Senior Research Associate - QC, Genomic Medicine Bioanalytics - CT Master’s degree in Biology/Biochemistry or related discipline. Exp: 0+ years |
This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi’s CMC Development organization. The GMU Analytical Development group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust analytical methods to support release and characterization testing of different cell therapy candidates. The group supports cGMP-compliant in-process Quality Control (QC) support of cGMP Manufacturing cutting edge methods such as flow cytometry. The selected candidate will execute rapid turnaround cGMP testing of in-process materials. In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month. | 9/29/2023 |
| 3995 | ProteinSimple Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in Molecular Biology or equivalent. Exp: 0-2 years |
The responsibilities of this position are to assist the protein product development team in the area of recombinant protein expression. This includes the preparation of eukaryotic expression vectors, cell culture, and screening procedures. The successful candidate will perform various techniques such as DNA preps, sub-cloning, mammalian and insect cell culture, transfections, Western blotting, ELISA, and flow cytometry. They will also prepare buffers and reagents, assist in cleaning and maintenance of the laboratory and equipment, and perform other general lab duties as assigned. | 9/29/2023 |
| 3996 | ProteinSimple Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 9/29/2023 |
| 3997 | NorthEast BioLab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: Entry Level |
NOTE: PLEASE SUBMIT BOTH RESUME AND COVER LETTER TO APPLY FOR THIS JOB. KINDLY DISCUSS YOUR MOTIVATION, RELEVANT EXPERIENCE, SALARY REQUIREMENTS, AND VISA STATUS IN YOUR SUBMISSION. If interested, please e-mail your resume to careers@nebiolab.com. Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices Follow appropriate safety and study requirements by reading, understanding, and following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) requirements, and Sponsor Study protocols Support business development and marketing activities, foster client relationships, and help onboard new sponsors | 9/21/2023 |
| 3998 | Nephron Pharmaceuticals West Columbia, SC Microbiology Quality Specialist Bachelor’s degree Exp: 1 year |
Position Summary: Responsible for timely review of laboratory data, Standard Operating Procedures (SOPs), Equipment Validations, studies, and other documents related to the Microbiology department, as needed. Creates and executes project review plans; ensures timely completion of studies or assigned special projects to meet changing needs, requirements, and deadlines of the Microbiology department. Assists with additional work duties or responsibilities as evident or required | 9/21/2023 |
| 3999 | Nephron Pharmaceuticals West Columbia, SC Microbiology Quality Investigator Bachelor’s degree preferred. Exp: 1-2 years |
Position Summary: Assures compliance with FDA regulations in the areas of non-conformance investigations, memorandums, deviations, and corrective and preventive actions (CAPA’s) for the Environmental Monitoring (EM) department. Works effectively with other departments to ensure timely completion of projects, as well as effective management of individual workloads. Performs other duties as assigned or apparent. | 9/21/2023 |
| 4000 | Nephron Pharmaceuticals West Columbia, SC Microbiology R&D Analyst I · Regionally accredited Master’s Degree in Microbiology or other science-related field. Exp: 1 - 3 years |
Position Summary: Performs research and develops projects for both established and new products, including, but not limited to, microbiological test method validation/transfer/verification, procedures, investigations, and other non-specified projects or initiatives. Plans, organizes, and manages resources on method validation projects to assure technical quality and schedule adherence. Performs other duties as assigned or apparent. Works with different microbiological techniques and equipment, including but not limited to gram stain, turbidimetric endotoxin testing, liquid particle counter, isolator, bioburden, filtration analysis, sterility testing, aseptic process simulation, and MALDI-TOF. Performs different microbiological tests for R&D Microbiology and QC Microbiology, as needed; also understands and performs routine investigations related to Environmental Monitoring and laboratory testing. Works in a GMP environment and responsible for generating cGMP data. Plans and executes research and test method development projects for both established and new products. Participates in development and implementation of associated programs (e.g. cleaning validation, process validation, cGMP compliance, equipment validation, maintenance and use, etc.), as well as generating trending reports for cleanroom environments. Participates in reading and documenting media fill results. Works in a cGMP environment and is responsible for generating cGMP data. Ensures reports, submission documentation, and development summaries documenting the product development process are available for clients, partners, and health authorities (i.e. FDA). Assists in drafting R&D and QC protocols, summary reports, and studies. | 9/21/2023 |
| 4001 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Second Shift (Sun. - Thurs. - 2:00pm to 11:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
Position Summary: • Support quality control testing and research and development activities as needed. • Assists with additional work duties or responsibilities as evident or required. • Performs other duties as assigned or apparent. • Relies on instructions and pre-established guidelines to perform job functions. • Works under immediate supervision. • Relies on instructions and pre-established guidelines to perform job functions. • Works under immediate supervision. | 9/21/2023 |
| 4002 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - First Shift (Mon. - Fri. - 8:00am to 5:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
Position Summary: • Support quality control testing and research and development activities as needed. • Assists with additional work duties or responsibilities as evident or required. • Performs other duties as assigned or apparent. • Relies on instructions and pre-established guidelines to perform job functions. • Works under immediate supervision. | |
| 4003 | Nexcelom Bioscience San Diego, CA Research Associate I - Protein Purification Bachelor’s Degree in biological sciences. Exp: 0 - 1 year |
This position is responsible for developing recombinant protein research products in the Molecular Cellular Biology group by using cutting-edge synthetic biological technology. The duties include preparing buffer solutions and E. Coli cell culture media, performing bacterial cell cultures, and purifying recombinant proteins with affinity tag, performing protein characterization according to standard operating procedures. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 9/22/2023 |
| 4004 | Nexcelom Bioscience Pittsburgh, PA Associate Specimen Processor Associate or Bachelor's degree in a life sciences discipline. Exp: 0-1 year |
KEY RESPONSIBILITIES Receive and process clinical samples within the guidelines of the site working procedures. Enter data into laboratory information systems. Split down and remove excess packaging to reduce waste footprint within the building. Transfer from and to internal lab areas in a timely manner. Demonstrate thorough knowledge of accessioning processes and quality control. Ensure Good Documentation Practices (GDP) are followed, including proper specimen handling, labelling and preparation of required documents. Other duties as assigned by Supervisor | 9/22/2023 |
| 4005 | Nexcelom Bioscience Boston, MA Associate Chemist B.S. degree in a Life Sciences field. Exp: 0-4 years |
We are seeking a bachelor's level candidate to join a team of scientists manufacturing synthetic chemical products used throughout the world in scientific research applications. This position will function as a member of the production staff and will participate in the transfer, implementation and on-going production of products in the laboratory. | 9/22/2023 |
| 4006 | Nexcelom Bioscience Lafayette, CO Associate Scientist Bachelor's Degree in Life Sciences. Exp: 0-3 years |
This is a 2nd shift position- 4-day work week– Monday-Thursday 12pm-10:30pmMT. Job Summary: Revvity has a rewarding and exciting opportunity for an Associate Scientist for our Synthetic Manufacturing laboratory. The Associate Scientist position will perform primary tasks in an ISO 9001:2015 laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the manufacturing, processing, and packaging of RNA and DNA oligonucleotides. This includes synthesis, cleaving, quality and quantity determination, purification, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry in multiple laboratories. | 9/22/2023 |
| 4007 | Nexcelom Bioscience San Diego, CA Research Associate II - Product Development (Cell Analysis) Bachelor or Master’s degree in a Life Science related field. Exp: 1+ years |
BioLegend is seeking a self-motivated Research Associate to join our Product Development team in San Diego. The incumbent will actively participate in all the stages of the development, optimization, and validation of new products. This position will have the opportunity to interact with multi-disciplinary teams. The work requires routinely handling small animals and biological samples from animals and human donors. Prior experience in tissue culture, flow cytometry, immunoassays, molecular biology techniques (eg PCR, cloning, etc), data analysis, and project management are preferred | 9/22/2023 |
| 4008 | Northstar Medical Technologies Beloit, WI Manufacturing Engineer Bachelor’s Degree in Engineering Exp: 0+ years |
The Manufacturing Engineer is responsible for evaluating manufacturing processes by assisting in the design and conduction of research programs; applying knowledge of product design, fabrication, assembly, tooling/equipment, and materials. This position will assist in coordinating product and process improvements to meet quality and production goals. All duties and responsibilities will be done in compliance with cGMP and FDA regulations. | 9/22/2023 |
| 4009 | Nostrum Laboratories Kansas City, MO Chemist I Bachelors Degree in Chemistry, Pharmaceutical, Biology or a science related field. Exp: 0+ years |
General Summary Description The Chemist I is responsible for developing and validating test methods; validating laboratory instruments; conducting lab testing for raw materials, components, in-process materials, finished products, stability, and other samples in accordance with cGMP regulations, regulatory filings, and approved procedures. | 9/22/2023 |
| 4010 | Nostrum Laboratories Bryan, OH Chemist I Bachelors Degree. Masters Degree or PhD. preferred. Exp: BS: 0 - 4 years; MS or PhD: 0 - 2 years |
General Summary Description Responsible for development and validation of analytical methods in support of product development and IND/NDA/ANDA filings. Perform routine wet chemical and instrumental analysis on raw materials, in-process, finished and stability products. Accurately compiles and reports data. Gather, compile and compose documents needed for regulatory submissions | 9/22/2023 |
| 4011 | Nostrum Laboratories Bryan, OH MICROBIOLOGIST I Bachelors Degree in Biology or Microbiology. Exp: 0+ years |
Perform all testing on in-house and contract samples as needed: o In-process o Finished product o Stability o Raw material (including water) o Environmental Testing | 9/22/2023 |
| 4012 | Nostrum Laboratories Bryan, OH METROLOGIST I Bachelors Degree in Chemistry or Physical Science. Exp: 1 - 2 years |
Duties and Responsibilities Develops calibration methods and techniques based on principles of measurement science, technical analysis of measurement problems, and accuracy and precision requirements Identifies magnitude of error sources that contribute to uncertainty of results to determine reliability of measurement process in quantitative terms Calibrates/qualifies a variety of process laboratory equipment, measurement/control instrumentation, and software Conducts daily calibration check as needed Schedule and perform calibrations according to SOPs or manufactures procedures on Measurement and Test Equipment insuring schedule work requirements are met Completes all calibration certificates Ensures accuracy, reliability, and compliance with operating procedures Performs data entry functions required to update the calibration database, as required Initiates instrument/document change control as necessary Maintains documentation according to SOPs and cGMP requirements Writes, develops, and reviews Standard Operating Procedures | 9/22/2023 |
| 4013 | Nova Biomedical Waltham, MA Associate Scientist B.S./ B.A. Degree in Chemistry, Biology, Biomedical engineering or related field Exp: 0-2 years |
Nova Biomedical is looking for an Associate Scientist to join our Organic Research Lab in Waltham, MA. In this role, you will work within a multi-disciplinary team to conduct the research and development of chemical/biological sensors, assays, and reagents for the clinical analyzers and instrumentations | 9/22/2023 |
| 4014 | Nova Biomedical Waltham, MA Quality Engineer I Undergraduate Degree with a concentration in the sciences. Exp: I -2 years |
Nova Biomedical is hiring a Quality Engineer to be responsible for testing and ensuring the quality of all products manufactured by Nova Biomedical in the Waltham, MA facility. You will manage the qualification of processes and equipment, ensuring that all processes are performed according to established procedures and working with Research and Development and Manufacturing Engineering to remedy issues encountered. You will ensure that Quality Systems practices are an integral part of planning, production, and analytical activities using engineering, scientific, and technical principles. | 9/22/2023 |
| 4015 | Nova Biomedical Waltham, MA Supplier Quality Engineer BS degree in an Engineering discipline. Exp: I year |
Nova Biomedical is hiring a Supplier Quality Engineer in our Waltham, MA office to support programs to qualify suppliers and improve supplier performance and productivity. More specific responsibilities include: Support the ongoing maintenance of the Approved Suppliers List (ASL) through the following activities: Updating the contents of the ASL as required, and as directed. Support the initial evaluation for new suppliers. Support the qualification activities for high-risk suppliers by participating in remote and onsite supplier audits. Requalify existing suppliers by performing desktop surveillance audits. Maintain all supplier qualification-related documentation. Generate periodic supplier performance reports and provide them to suppliers. Support the Nova Supplier Change Notification (SCN) process. Initiate SCNs as the result of having received a supplier-generated Product Change Notification (PCN) or other supplier generated notification of a required change. Manage the SCN database. Support the disposition of Nonconforming Material Reports (NCMR) and issuing Supplier Corrective Action Requests (SCAR) as directed. Maintenance activities för the NCMR, SCAR, and SCN databases. | 9/22/2023 |
| 4016 | Novartis Cambridge, MA Research Scientist / Senior Scientist, Preclinical Safety, Pathology, Immunology – Dual Posting Research Scientist: Education: bachelor’s or master’s degree or equivalent in immunology, cell biology or Medicine. Exp: 0-5 years |
We are seeking to hire a motivated candidate with a strong background in cellular and molecular immunology to join our Immunology Group in Cambridge, MA. The candidate will support cross-species in vivo and in vitro immunology testing using preclinical models, including non-human primates, towards non-clinical safety assessment and to address key scientific questions on comparative biological responses to novel medicines, bridge gaps in translational immunology and explore hematopoietic system physiology. You’ll also have continuous opportunity to work with other Novartis experts in flow cytometry, immunology, and related scientific and technical areas to expand your learnings. Ultimately, you will improve and accelerate Novartis drug discovery and development processes aimed to bring forward effective and safe medicines. | 9/22/2023 |
| 4017 | Novartis Cambridge, MA Research Scientist Biochemistry, CVM BS or MS degree in biochemistry, molecular biology, cell biology, biophysics, biomedical engineering, or a related field. Exp: 1+ years |
We are seeking a highly motivated in vitro Research Scientist to join our Biochemistry team. Here you will advance our understanding of disease biology and the discovery of new drugs, by contributing to target validation, assay development and drug screening efforts throughout the disease area and in collaboration with the larger research organization. As a biochemistry and cell biology Research Scientist, you will conduct experiments both independently and collaboratively in an inter-disciplinary setting to support drug discovery projects | 9/22/2023 |
| 4018 | Novavax Gaithersburg, MD Research Associate II, Formulation Development Bachelor degree or a Master degree in a formulation development relevant field. Exp: 1 to 2 year |
Responsibilities include but are not limited to: Perform rapid, comprehensive characterization of candidate drug products to determine the physicochemical properties of the drug product and evaluate them for further drug development programs including: AUC, CD, Fluorescence spectroscopy, DSC, ITC, UV/Vis spectroscopy, FTIR, SLS and HPLC. Percentage of time (Approx): 65% Assist in the development and scale-up of drug product processes from bench top to pilot scale and technology transfers. Percentage of time (Approx): 10% Provide support to formulate small and large scale lots of liquid, frozen or lyophilized drug substance/product samples. Percentage of time (Approx): 5% Assist in development of formulation studies and design protocols. Percentage of time (Approx): 5% Project management of other research associates in support of the larger drug development project. Percentage of time (Approx): 5% Write technical reports and applicable SOPs. Percentage of time (Approx): 5% Responsible for preparing data summary presentations, compiling data and authorizing technical reports. Percentage of time (Approx): 5% | 9/22/2023 |
| 4019 | Novavax Gaithersburg, MD Associate II, Analytical Development Bachelor’s degree OR Master’s degree. Exp: BS:1-2 years; MS: 0-1 year |
Novavax is seeking an Associate II, Analytical Development to provide technical and documentation support in a laboratory setting. This role is responsible for contributing to the method development, qualification, and technology transfer for analytical methods. The qualified individual will bring experience in relevant analytical technologies, such as ELISA, VaxArray, Luminex, or BLI. The position will perform in-process testing, as needed, to support the Process Development, Formulation Development, and Manufacturing teams, in addition to method development and qualification. This position will report to the Sr. Scientist, Analytical Development. | 9/22/2023 |
| 4020 | Novo Nordisk Lexington, MA Research Associate - ADME B.S./M.S. in a scientific discipline, analytical chemistry, chemistry, biochemistry, biotechnology or related discipline preferred. Exp: 0+ years |
We are seeking a Research Associate - Absorption, Distribution, Metabolism and Excretion to help support the development of our growing pipeline of product candidates. The individual in this position will assist in the conduct of nonclinical studies and the ADME assays and sample analysis. | 9/22/2023 |
| 4021 | Novo Nordisk Clayton, NC Associate Process Engineer - Site Capacity bachelor’s degree within engineering or natural sciences, manufacturing or similar which could be as mechanical engineer, process engineer, consultant Exp: 0-3 years |
Fill-Finish Expansion is seeking a Robotic Engineer for the Material Handling Work-Package. In this role, you will play a crucial role in creating future standards for equipment that handles incoming materials for filling lines and transforming existing manual processes into fully automated ones. As a Robotic Engineer, you will leverage your expertise in automation to collaborate with us and future vendors in developing, designing, and producing the solutions Novo Nordisk needs for future facilities worldwide. To succeed, you must bring relevant automated material handling and/or robotics experience, harvest the existing knowledge of the company, and combine the inputs into state-of-the-art material handling technology solutions while working with local and global stakeholders. Your overall objective is to conceive and develop robotic solutions to optimize our manufacturing through traditional automation and robotics. | 9/22/2023 |
| 4022 | Novo Nordisk Fremont, CA Engineer I Bachelor’s degree Exp: 0- 1+ years’ |
The Engineer I will make significant contributions to the research of life changing medical devices at Novo Nordisk (NN). They leverage their strong background in engineering to perform their individual tasks as well as energetically engaging in collaborative work. The Engineer I will contribute to insert subject matter expertise. They ensure strong progress on research initiatives under the broad direction of more senior engineers and management. | 9/22/2023 |
| 4023 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 9/22/2023 |
| 4024 | Nucelis San Diego, CA Research Associate, Analytical Chemistry BS/BA or MS in Chemistry or related scientific discipline. Exp: 1+ years |
We are seeking a highly capable and energetic analytical research associate (RA or Senior RA) that is willing to work as part of a team to isolate, identify, quantify, and characterize natural products from our engineered systems. This role will require routine execution of established analytical protocols and the ability to work independently as we support company-wide research projects in the analysis of plant and fermentation analytes. The ideal candidate will have hands-on experience with analytical instrumentation (GC/MS, LC/MS, HPLC) and experience with natural product identification, quantification, and characterization and/or have a desire to gain significant experience in these areas. | 9/22/2023 |
| 4025 | Nutcracker Therapeutics Emeryville, CA Research Associate/Sr. Research Associate, Analytical Development (Contract) Bachelor’s or Master’s degree in a relevant field, e.g. Biochemistry, Molecular Biology, Chemistry, Bioengineering Exp: one year |
We are looking for a talented RA/SRA (contract) to join the Analytical Development team in support of process and product characterization. This individual is a motivated self-starter who thrives by generating high-quality data in the laboratory. The ideal candidate is also looking for a challenging work environment that provides opportunities for collaboration and growth. If you are driven to discover, create, and inspire something that moves science and technology forward, and lasts a lifetime and beyond, you’re ready to be a Nutcracker. This is a contract position lasted an expected 6 months | 9/22/2023 |
| 4026 | Nvigen Campbell, CA Laboratory Technician Bachelor’s degree in chemistry or biology preferred. Exp: 0+ years |
Familiar with standard chemical or molecular laboratory techniques and practices. Primary responsibilities will include assisting researchers with sample processing, assay evaluation and improvement. Must be able to follow detailed protocols with minimal supervision. Successful candidate will be highly motivated, eager to learn, and be able to meet the challenges of a fast-paced environment. Must possess excellent attention to detail, be organized and can maintain detailed records. Must have good communication skills and be able to work effectively independently and in a team. Support general lab management duties such as ordering supplies, maintaining equipment and organization. Prior experience in biological or chemical laboratory required. | 9/22/2023 |
| 4027 | Ocean Ridge Biosciences Concord, OH Laboratory Technician - Genetic Toxicology Bachelor’s degree in biology, microbiology, chemistry, or a related field. Exp: 1+ years |
We are currently seeking a Lab Technician to join our team and provide technical support for performing standard genetic toxicology assays. This position will play a crucial role in our laboratory operations, which include various cell-based assays, bacterial reverse mutation assay, rodent bone marrow and blood based micronucleus assays, and other related in vitro activities. | 9/22/2023 |
| 4028 | Ocean Ridge Biosciences Chicago, IL Assistant/Associate Toxicologist BS degree in animal/veterinary science, biology, or related disciplines. AALAS accreditation is a plus. Exp: Associate Toxicologist: 0-3 years |
Position/Job Summary: The Associate/Assistant Toxicologist plays a key, hands on role in the conduct of preclinical studies and supports the Study Director to ensure that Sponsor studies are conducted properly and according to FDA guidelines. | 9/22/2023 |
| 4029 | Ocean Ridge Biosciences Hayward, CA Research Assistant - Bioanalytical Services B.S. degree in related scientific discipline. Exp: 0-3 years |
Job Summary 1) Assist lab work and method development 2) Follow SOP and protocol to conduct method validation and sample analysis under supervision 3) Comply with GLP regulations in lab work and documentation 4) QC review data and reports 5) Perform instrument setup, maintenance, and basic trouble-shooting under supervision 6) Strictly follow SOPs and regulations to serve as sample coordinator. | 9/22/2023 |
| 4030 | Olympus Indianapolis, IN Field Service Engineer I (Indianapolis, IN) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4031 | Olympus Orlando, FL Field Service Engineer I (Florida, Orlando) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4032 | Olympus San Antonio & Austin, TX Field Service Engineer I (Texas) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4033 | Olympus New York City, NY Field Service Engineer Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4034 | Olympus Boston, MA Field Service Engineer I (Boston, MA) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4035 | Olympus Cincinnati, OH Field Service Engineer I (Cincinnati, Ohio) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4036 | Olympus San Jose, CA QA Engineer I Bachelor’s Degree in Engineering or Scientific Discipline (or equivalent). Exp: 0-2 years |
Job Description The Quality Assurance Engineer I is responsible for providing Quality Engineering input to support Production, Operations and Engineering activities. Maintains and follows Quality Engineering methodologies, systems, and practices which meet Olympus, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility and communication on Quality initiatives to support departmental, functional, site, divisional and corporate Quality goals and priorities. When needed, works with Olympus Tokyo representatives/liaisons to resolve Quality related issues. | 9/22/2023 |
| 4037 | Lonza Portsmouth, NH Biotech Nights Manufacturing (Entry and Junior Level Positions) AS/BS preferred; Science related discipline Exp: 1+ years |
This posting is for candidates interested and willing to work night shifts: The night shift schedule is from 7pm-7am, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends and nights worked Are you seeking to kickstart your career in the manufacturing or life sciences industry? Or perhaps you already have some experience and are looking for the next challenge? We have openings for entry to junior level manufacturing associate positions here at Lonza in Portsmouth NH. If you're detail oriented, motivated, and eager to learn, this could be the perfect role for you! Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. | 9/14/2023 |
| 4038 | Lonza Portsmouth, NH Biotechnologist Level 1 (Nights) AS/BS preferred; Science related discipline Exp: 1+ years |
The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. Level III associates are expected to be SMEs on all core functions in the suite with anticipated cross training into other manufacturing areas within the asset. Senior associates are expected to be expert within operations and lead the manufacturing team from a technical perspective. Senior associates are expected to be proficient in trouble shooting, appropriate escalations and are able to facilitate a path forward to maintain safety and quality for the product. Shift Schedule: The shift schedule is from 7pm-7am, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends and nights worked Initial 2 week training period on day shift Monday-Friday upon hire | 9/14/2023 |
| 4039 | Lonza Portsmouth, NH Biotechnologist II (A Shift Days) AS/BS preferred; Science related discipline Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends and nights worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks.Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends and nights worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires | 9/14/2023 |
| 4040 | Lonza Houston, TX Core Technician - Viral Vector / Cell Therapy Bachelor’s or Associate’s Degree in Life Sciences Exp: 1+ years |
Lonza Cell and Gene Therapy is the largest in the world and our Houston, TX site is growing. As a Core Technician in Viral Vector or Cell Therapy, you will be working at, and learning from, one of the industry leaders. We are world-class manufacturing experts, who strive for continuous improvements in environments where change is constant. You will be part of a team, performing a variety of tasks involved in the production of sterile biological pharmaceutical products and collaborating closely with your colleagues to deliver innovative processes. As we run a 24/7/365 operation, roles may include working a variety of shifts, including nights and weekends. | 9/14/2023 |
| 4041 | Loxo Oncology San Diego, CA Contract Scientist/Senior Scientist (Non-PhD), Protein Expression MS in protein sciences, biology, biochemistry, molecular biology, life sciences or a related field. Exp: 1+ years |
This Contract position offers the opportunity to be part of Loxo@Lilly’s discovery teams focused on creating novel, highly specific and selective drugs for genetically identified targets. The Contract, Protein Scientist will support the internal and external discovery research efforts across multiple projects and project teams. This is an extremely important role where the right person will be able to have a real impact on cutting-edge science, making a real difference in patient’s lives | 9/15/2023 |
| 4042 | LSI Solutions Victor, NY Process Validation Engineer Process Validation Engineer I: Bachelor’s Degree in an engineering, technical or manufacturing discipline. Exp: 1-3 years' |
The Process Validation Engineer will develop and execute validations to ensure regulatory compliance to established internal and external standards related to released product or current production. The individual will support the writing of validation protocols and reports, along with the gathering and analysis of data. | 9/15/2023 |
| 4043 | LSI Solutions Victor, NY Product Design Engineer Product Design Engineer I: Bachelor’s Degree or higher in Engineering or related technical discipline required. Exp: 0-3 years |
Supports introduction of new products by leading and maintaining all Product Engineering related activities. Senior Product Design Engineer provides functional expertise, leadership, and mentorship to the Product Engineering function. | 9/15/2023 |
| 4044 | LSI Solutions Victor, NY Manufacturing Engineer - Days (8am to 5pm) Level I: BS Engineering or Engineering Tech. Exp: 0-3 years |
The Manufacturing Engineer under R&D is responsible for leading the development, selection, and transfer of manufacturing processes during New Product Development (NPD) projects. This role supports equipment qualification and process validation activities as well handling development of workflows, assembly methods, and risk assessment tools to define a process that meets the project requirements. | 9/15/2023 |
| 4045 | LSI Solutions Victor, NY Manufacturing Engineer II (Days) Level II: MS Engineering Exp: 1 to 5 years |
The Manufacturing Engineer is responsible for manufacturing process performance, receiving new products transfer into series production, product and problem diagnosis and repair. Support the development, qualification, verification, and validation of changes to existing product and manufacturing processes. Maximizes efficiency by analyzing equipment layouts, workflow, assembly methods, and work force and equipment utilization. Develop short- and long-term operational strategies in partnership with senior team members and provide the leadership necessary for the successful design, development, and execution of that strategy to achieve measurable outcomes in a timely, cost-effective manner. | 9/15/2023 |
| 4046 | LSI Solutions Victor, NY Regulatory Associate - Days 8am to 5pm Regulatory Associate I: Bachelor or Master’s degree in a technical, regulatory, or life sciences discipline Exp: RAI: 0-2 years’ ; RAII: 1-2 years’ |
The Regulatory Associate applies her/his experience, knowledge, organization skills, and communication skills in a wide variety of tasks. All Regulatory Associates provide regulatory feedback and guidance based on medical device regulations and standards to the company throughout the development cycle. Regulatory Associates monitor regulations, standards, policies, and guidance for new and current compliance requirements that may have impact to the company. Regulatory Associates maintain technical documentation and help to implement change control at LSI. Regulatory Associates are assigned to work in one or more of the following areas: Domestic, European, Rest of World, Labeling, and/or Clinical & Post Market Surveillance. Regulatory Associates assigned to Domestic projects will contribute to regulatory strategies for design and development projects and contribute to regulatory submissions to the FDA when appropriate. Regulatory Associates assigned to European regulatory projects will be involved with medical device classification, preparation of technical documentation, conformity assessments, and notices of change in compliance with the EU MDR and associated guidance. Regulatory Associates assigned to Rest of World projects will work with distributors to provide documents for regulatory submissions required to market LSI’s new or modified medical devices in many countries outside the U.S and Europe. Regulatory Associates assigned to Labeling projects apply knowledge of U.S. and international regulations and standards with highly cross-functional teams to ensure compliance for IFU, UDI, and promotional material requirements. Regulatory Associates assigned to Clinical projects contribute to clinical evaluation, investigator brochures, post-market clinical follow-up, and post market surveillance. All Regulatory Associates will also maintain full Quality and Regulatory compliance with all standards that govern the design, development, manufacturing, and distribution of our medical devices. | 9/15/2023 |
| 4047 | Lumen Bioscience Seattle, WA Lab Technician BA/BS degree in molecular biology, biochemistry, biotechnology, microbiology or related field of study. Exp: 1-2 years |
Lumen is seeking a highly motivated and detail-oriented Laboratory Technician to join our team. The Laboratory Technician will closely work with other scientists in the R&D group to develop biologics using Lumen’s spirulina-based expression system. The individual is expected to handle and maintain cyanobacterial cultures; perform standard molecular biology techniques such as PCR, bacterial cloning, bacterial transformation, plasmid purification and gel extraction; and contribute to general lab housekeeping. The position requires the ability to work independently with minimal supervision as well as within a team. It also requires significant attention to detail and the ability to track a large amount of processes and samples occurring in parallel. A successful candidate should also be comfortable assisting other laboratory personnel in the development and application of new techniques. The position requires the ability to work as a team member in a fast-paced environment and to assist other laboratory personnel as needed. It is central to Lumen’s acquisition and integration of new and complex technologies, and to sharing such capabilities with other teams, and as such, flexibility and independence will be essential. The position requires strong organizational skills and meticulous laboratory record keeping. Effective communication skills are crucial in coordinating with the relevant teams to meet milestones and deadlines and in raising quality or troubleshooting issues as they may arise. The position includes providing status updates and presenting in group and company-wide meetings. | 9/15/2023 |
| 4048 | Lung Biotechnology Manchester, NH Research Associate I/II - Cell Production & Process Development Master’s Degree in cellular biology, developmental biology, biomedical engineering or related field Exp: 1+ years |
The Research Associate II – Cell production and Process Development will perform and contribute to the design of cell studies as well as execute analytical methods to support the production and process development of iPS-derived cells and cellularized 3D scaffolds for the development of autologous 3D printed tissue engineered organs. | 9/15/2023 |
| 4049 | Lung Biotechnology Manchester, NH Research Associate II - Tissue Systems Master’s Degree in cell biology, biomedical engineering or related field Exp: 1+ years |
The Organ Manufacturing group (OMG) at Lung Biotechnology focuses on identifying, scoping, and delivering projects in support of our mission to build cutting edge technology for organ scaffold 3D bioprinting to address the unmet needs for transplantable organs. The Research Associate II-Tissue Systems will work with the direct supervisor to establish new experimental procedures and analytical metrics to characterize the biological outcomes of different lung cell types on 3D printed lung scaffolds. | 9/15/2023 |
| 4050 | Lykan Bioscience Hopkinton, MA QC Analyst, Microbiology Bachelor's degree in scientific discipline preferred. Exp: 0-2+ years' |
The Quality Control Analyst, Microbiology will be responsible for collection of environmental and raw material samples, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 9/15/2023 |
| 4051 | Marker Therapeutics Houston, TX Cell Therapy Manufacturing Technician BS, MS in Biology or a related science Exp: 1-5+ years |
Marker Therapeutics is seeking a cell therapy technician for its manufacturing group to support its ongoing efforts to develop immunotherapies for the benefit of patients with cancer. This position will work under the guidance of the Senior Director of CMC and perform assigned responsibilities to support the company’s product manufacturing process and process improvement initiatives. Depending on previous experience and qualifications, this individual will be expected to either lead or support the manufacturing process and process characterization of scale-up/scale-down cell manufacturing processes, including optimizing process parameters, cell concentrations and therapeutic product fill and finish technologies to advance our therapeutic programs. The successful candidate must be a team player with strong expertise in GMP manufacturing and must have the ability to communicate and collaborate within an interdisciplinary environment. | 9/15/2023 |
| 4052 | Maverick Therapeutics Social Circle, GA Filling and Packaging Engineer I Bachelor’s degree in Engineering discipline required. Exp: 1+ years |
The Filling and Packaging Engineer, reports to a Production Manager and is responsible for on-shift operational support of the IG department in Covington, GA. The Filling and Packaging Engineer focuses on rapidly resolving manufacturing problems, enabling manufacturing to meet production goals. As a member of the operations team, you will provides on-shift technical knowledge and leadership. | 9/15/2023 |
| 4053 | Medpace Cincinnati, OH Biology Laboratory Technician Bachelor's degree. Exp: 1+ years |
Responsibilities Prepare samples according to project protocol and/or related SOPs; Maintain compliant laboratory documentation; Perform data analysis and data checking; Interpret results obtained for accuracy and acceptability; Clean and sterilize laboratory equipment; and Other duties deemed necessary. | 9/15/2023 |
| 4054 | Medpace Cincinnati, OH Chemistry Laboratory Technician Bachelor's degree. Exp: 1+ years |
Responsibilities Prepare samples according to project protocol and/or related SOPs; Maintain compliant laboratory documentation; Perform data analysis and data checking; Interpret results obtained for accuracy and acceptability; Clean and sterilize laboratory equipment; and Other duties deemed necessary. | 9/15/2023 |
| 4055 | Medtronic Danvers, MA Quality Engineer II Advanced Degree in Engineering, Science or technical field. Exp: 0+ years |
In this exciting role as a Quality Engineer II, you will have responsibility for the manufacturing transfer project(s) between sites which includes activities related to test method validation, process validation, design validation, inspection training, and process/quality change initiatives. This is an onsite role at the Danvers, MA location | 9/15/2023 |
| 4056 | Medtronic Brooklyn Park, MN Mechanical Design Engineer II Advanced Degree Mechanical Engineering. Exp: 0+ years |
Contribute to the development/sustainment of cardiac surgery disposable and capital goods products that meet application, business, customer, quality, and regulatory requirements. Such contribution includes collaborating with colleagues in Design, Research, Manufacturing, and Quality and preparing documentation, some of which may be submitted to regulatory agencies, in accordance with applicable procedures. | 9/15/2023 |
| 4057 | Medtronic Coon Rapids, MN Equipment Engineer II Advanced Degree Exp: 0+ years |
• Evaluates, selects and order equipment that is most appropriate and cost effective for the studies performed at PRL • Oversees the installation, upgrade and maintenance of equipment used in research operations, clinical lab, histology lab, necropsy areas, material characterization lab and biomaterials lab. • Maintain current records on equipment manufacturer’s technical notices, upgrades and safety issues. • Studies equipment performance and reliability • Establishes programs and solutions for increasing uptime and for equipment problems that affect the any PRL activity. • Provides technical support for the equipment repair. | 9/15/2023 |
| 4058 | Medtronic Littleton, MA Quality Engineer II - CST - Littleton, MA (Onsite) Advance degree in biomedical, Electrical, Computer, or Software engineering. Exp: 0 years |
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future. | 9/15/2023 |
| 4059 | Merieux NutriSciences Columbus, OH Microbiologist 1 Bachelors preferred. Exp: One (1)- 2 years |
Purpose (Objective): The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 9/15/2023 |
| 4060 | Merieux NutriSciences Crete, IL Chemist 1 Bachelors preferred. Exp: One - two years |
Purpose (Objective): The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. | 9/15/2023 |
| 4061 | Merieux NutriSciences Salt Lakre City, UT Chemist 1 Bachelors preferred. Exp: One - two years |
Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. Wash glassware as needed and prepare samples as needed. Prepare standards or reagents that are needed for the analysis procedure. Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. | 9/15/2023 |
| 4062 | Meso Scale Discovery Rockville, MD Manufacturing Technician I Degree in Biology, Chemistry, Biotechnology, Engineering or related field is preferred. Exp: 1+ years |
Production role in consumables, kit or reagent manufacturing responsible for meeting production schedules in a fast-paced, high throughput industrial setting. This may include the production of coated plates, chemical buffers, and biological diluents/reagents and/or assembled kits for customer order fulfillment. Some degree of professional latitude, creativity and self-management is expected. | 9/15/2023 |
| 4063 | Moderna Therapeutics Norwood, MA Engineer II, Manufacturing Science & Technology MS Biochemical engineer, Chemical engineer, or Biochemistry background. Exp: 1 to 3 years’ |
This position is part of Moderna’s Manufacturing Science and Technology (MST) team responsible for ensuring the robust technology transfer and technical support of our mRNA platform in cGMP Manufacturing. The individual will work closely within MST, and with Process Development, Manufacturing, Regulatory, and Quality, to ensure all aspects of technology transfer and technical support are successfully executed. The individual may also provide engineering support like method writing for process equipment used at Moderna’s cGMP manufacturing operations in Norwood, MA. | 9/15/2023 |
| 4064 | Moderna Therapeutics Norwood, MA Research Associate, Drug Product Development Masters or Bachelor’s Degree in on one of the following fields: Chemical Engineering, Biochemical or Biomedical Engineering, Pharmaceutical Sciences, Exp: post Master’s Degree: 0 – 2 years; post Bachelor’s Degree: 0 – 4 years |
We are seeking a highly skilled and motivated Research Associate in Drug Product Development, to work in a team developing Moderna’s sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support product concept development including process development and scale-up work, container development and conditions of use studies. The incumbent will support the development of compositions, aseptic fill/finish unit operations through the development and use of scale-down models, process characterization studies etc. Applicants should have relevant pharmaceutical sciences related experience with various aspects of drug product development. The applicant should have exceptional ability to plan, execute and report, to communicate and collaborate, and requires strong attention to detail while working in a fast-paced, interdisciplinary environment. | 9/15/2023 |
| 4065 | Moderna Therapeutics Norwood, MA Engineer II, MS&T MS. Biochemical engineer, Chemical engineer, Biochemistry or Biology background. Exp: 1 to 3 years’ |
The Engineer II, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Personalized Cancer Vaccine (PCV). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 2nd shift role and the individual will be working a Sunday through Wednesday schedule from 1:00pm until 11:00pm. | 9/15/2023 |
| 4066 | Moderna Therapeutics Norwood, MA Engineer II, Process Development Masters. Exp: 1-3 years |
The successful candidate must be able to work in a fast paced and highly dynamic environment, will have relevant academic and or industrial experience in drug delivery, process development or formulation development, and will be able to contribute to both process development and commercialization related activities. We seek applicants that are proactive, enthusiastic, and show a passion for their work. Applicants should have exceptional time management and communications skills with a strong attention to detail. Previous experience with chromatography, nanoparticle formulations, filtration technologies, mixing technologies, and/or tangential flow filtration is preferred. The position will support cross-functional teams across CMC, Research and Development, Pre-clinical and GMP Production, Quality, and Analytical Development. | 9/15/2023 |
| 4067 | Moderna Therapeutics Norwood, MA Engineer I, mRNA Process Development BS/MS degree in Bio/Chemical Engineering, Bio/Chemistry, Pharmaceutical Science, or related field Exp: 0-3 years |
Moderna is seeking an Engineer I to join the mRNA Process Development team to support development, scale up, transfer and commercialization of drug substances based on mRNA and lipid nanoparticle delivery technologies. Moderna is developing first-in-class mRNA-based vaccines and therapeutics. The mRNA is packaged into lipid nanoparticles for storage and delivery. The candidate will be focused on unit operations that are standard across the industry such as enzymatic reactions, normal and tangential flow filtration and chromatographic purification. The candidate will support commercial manufacturing processes and execute experiments to support deviation investigations and definition of appropriate process controls to increase process robustness. Applicants should enjoy working in a fast-paced, dynamic, and innovative environment. The successful candidate will possess strong skills in designing and executing high quality bioprocess experiments using quality by design (QbD) and Design of Experiment (DoE) methods, and will collaborate through cross-functional matrix teams. The person in this role will have the opportunity to develop on-line analytics, process modelling and process investigation support. Results will be presented to broader groups allowing great exposure to CMC Strategy, Regulatory, MS&T, and Quality. Prior experience of process development and process investigation accomplishments using scaled down models, QbD-principles and process characterization/modeling techniques are strong pluses. In this role, multi-day domestic and/or international travel (up to 20%) should be expected to support process investigations, support technology transfer and provide Person-in-Plant (PiP) support for commercial batches. The position will be based out of Moderna’s Norwood facility. | 9/15/2023 |
| 4068 | Moderna Therapeutics Norwood, MA Manufacturing Associate I, INT Drug Product, Nights STEM degree. Exp: 0-2 years’ |
A Manufacturing Associate I in the PCV Drug Product Operations group is responsible for vial filling, visual inspection, label and packaging (Fill Finish) of Moderna’s mRNA Drug Products. This position is located at Moderna’s GMP Manufacturing site in Norwood, MA. The shift in Fill Finish Drug Product Operations will be nights 12 hours 6:00PM-6:00AM on a 3 on/2 off/2 on/3 off/2 on/2 off schedule. The individual in this role will be part of a cohesive team responsible for supporting GMP mRNA-based medicines for evaluation in human clinical trials through execution of vial filling, visual inspection, and labeling and packaging activities. The successful candidate will be able to document all activities performed following cGMP guidelines and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Manufacturing Sciences and Technology, Quality Control, Quality Assurance, Logistics and Process Development Technology Transfer counterparts. | 9/15/2023 |
| 4069 | Moderna Therapeutics Norwood, MA Research Associate, Analytical Technical Operations BS in Biochemistry, Molecular Biology, or a related field Exp: 1-3 years |
Moderna is seeking a molecular biologist to join Technical Development’s newly established Sequencing Center. In this laboratory-based position, the individual will routinely process sequencing samples, operate, and troubleshoot instruments including ABI 3730xl, Echo, Illumina MiSeq, NovaSeq, plate readers and liquid handlers. Experience with lab automation is a plus. The candidate must thrive in a fast pace high throughput environment, have a collaborative spirit, and be curious and willing to learn new techniques to push process development forward. | 9/15/2023 |
| 4070 | MP Biomedicals Solon, OH Production Chemist Bachelor of Science in Chemistry, Biochemistry, or Biology Exp: 0-3 years |
The production chemist will be trained on two different product lines. This position will rotate training through two manufacturing areas that include Immunology and Molecular Biology Liquids. Learn and be responsible for a wide variety of product formulation tasks. Follow and optimize production processes while following safety protocols. Produce quality research products in a timely fashion to meet customer demand. | 9/15/2023 |
| 4071 | DPT Laboratories St Albans, VT Chemist – 2nd Shift Bachelor's degree. Exp: 0-2 years |
Key responsibilities for this role include: Performs and documents the analysis of samples following approved test methods Calculate, check, and/or review data. Assist with method development, validation and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 9/15/2023 |
| 4072 | DPT Laboratories Morgantown, WV Chemist I Bachelor's degree. Exp: 0-2 years |
Key responsibilities for this role include: Document laboratory activity in accordance with established procedures; including reagent preparation. Complete training as an Acquisition Controller on LC/MS systems. Demonstrate ability to understand and perform the major types of extraction methodologies employed within the lab Independently perform routine testing proficiently in accordance with all pertinent SOPs and lab practices Process and analyze data according to established procedures. Review data and associated documentation for compliance with Standard Operating Procedures. Operate analytical instrumentation including triple quadrupole HPLC-MS/MS systems and automated liquid handling workstations; including maintenance. Perform experiments in support of method development and validation with supervision. Prepare written responses to audit observations. The minimum qualifications for this role are: Must possess knowledge of Standard Operating Procedures, Guidelines, a basic understanding of chemistry, and OSHA regulations and procedures for the safe handling of chemicals. Must possess good communication and writing skills. Must possess the ability to multi-task and be accurate and precise. Must possess computer skills with working knowledge of Microsoft Office Suite, and instrumentation software. Position functions with supervision. Bachelor's degree (or equivalent) and 0-2 years of experience. However, a combination of experience and/or education will be taken into consideration. Ability to read and interpret complex business and/or technical documents. Ability to write comprehensive reports and detailed business correspondence. Ability to work with groups of people such as other departments and communicate known concepts. Ability to present to a group of departments. Proficiency in speaking, comprehending, reading and writing English are preferred. Ability to perform computations such as percentages, ratios, and rates. | 9/15/2023 |
| 4073 | Nanosyn Eagan, MN Microbiologist BS/BA in microbiology, biology or related field Exp: 1-2 years |
Element - Eagan is hiring a Microbiologist to work in a fast-paced environment directing laboratory-based studies evaluating antimicrobial products. The Microbiologist (a) performs and evaluates microbiological efficacy testing; (b) assists in data and report generation while maintaining a high level of scientific integrity; and (c) assists with and designs research and development (R&D) projects when implementing new methods or adapting current methods. | 9/15/2023 |
| 4074 | Nanosyn North Liberty, IA Microbiologist II Bachelor’s Degree in a laboratory science field from an accredited college or university. Certification by the American Society of Clinical Pathologis Exp: 1+ years |
Element has a current opening for a Microbiologist II at our North Liberty, IA location. Under general direction, the Microbiologist II performs moderate to highly complex laboratory testing and analysis on bacterial and fungal isolates to provide information to the SENTRY program, new drug development protocols and clinical trial protocols. Utilizes professional skill and judgement to perform a variety of microbiology procedures within the laboratory. | 9/15/2023 |
| 4075 | Natera San Carlos, CA Research Associate 2 B.S. degree in molecular biology, related field, or equivalent. Exp: 1-2 years |
The Research Associate 2 works under the guidance of a Sr Manager to execute verification and validation (V&V) studies, under design control, for next generation sequencing (NGS) assays. Works hands-on at the bench to carry out experiments, makes detailed observations, analyzes data and interprets results. | 9/15/2023 |
| 4076 | Natera San Carlos, CA Research Technician BS/BA in a biological science or equivalent required. Exp: 1-2 years |
The Research Technician performs routine laboratory research and development services. Works with a multidisciplinary team. Under nominal direction, performs a variety of basic and general laboratory research and sample management tasks determined by the field and scope of the research project. | 9/15/2023 |
| 4077 | Aliri Bioanalysis Salt Lake City , UT Analyst I Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
Learns to analyze samples for various compounds and components in compliance with SOPs and regulatory agency guidelines. | 9/6/2023 |
| 4078 | Werfen Orangeburg, NY Scientist II Master's Degree Exp: 1 year |
Performs a broad range of laboratory work requiring application of professional judgment in the selection of specialized methods and techniques, and their application to specific tasks. | 9/18/2023 |
| 4079 | Inscripta Burlingame, CA Research Associate II/III, HTS BS/MS in Biology, Chemistry, Biochemistry or Chemical Engineering Exp: 1-2 years |
We are seeking a Research Associate II/III in our Burlingame location. The candidate will be a part of the high-throughput screening group, with primary responsibility for running screening operations for high-value products made by engineered strains of E. coli, S. cerevisiae, and other microbes. In addition, the candidate will contribute to the development and optimization of new high throughput and microfermentation assays, including automated sample preparation. They will work collaboratively with the rest of the team to optimize strain performance using our GenoScalerTM technology platform in rapid phenotyping of microorganisms. This hands-on position requires a desire and ability to work as a part of a multidisciplinary team, the ability to follow SOPs and run consistent operations, and an interest in continuously developing and improving our ability to characterize production strain through high throughput screening. | 9/6/2023 |
| 4080 | Integral Molecular Philadelphia, PA Research Associate I - (Job ID# 04182023) Bachelor’s degree in biology, bioengineering, or a related field? Exp: 1–2 years |
We are searching for a Research Associate I to join our dedicated group of scientists on the development and commercialization of biomedical technologies. We need someone who can effectively manage the challenges of performing high throughput assays, be self-reliant when executing tasks and contribute as a collaborative, supportive team member. A desirable candidate will have the skills to culture mammalian and/or bacterial cells, perform DNA mini-preps, and complete bacterial transformations and cell transfections. Familiarity with flow cytometry and liquid handling robots are a plus! | 9/6/2023 |
| 4081 | Ionis Pharmaceuticals Carlsbad, CA Research Associate, Cardiovascular Drug Discovery BS/MS in biology, molecular biology, biochemistry or related field. Exp: 1+ years |
The Cardiovascular, Renal & Metabolism (CVRM) Drug Discovery group seeks a Research Associate to join a multi-disciplinary team of energetic researchers who are working on validating new targets for cardiometabolic and renal diseases. The successful candidate will be responsible for the execution and analysis of studies utilizing rodent models of cardiometabolic disease as well as the evaluation of potential therapeutics for the treatment of heart failure. We are looking for a motivated individual with a strong attention to detail, capable of multi-tasking and who would succeed in a high paced atmosphere with minimal supervision. | 9/6/2023 |
| 4082 | Ionis Pharmaceuticals Carlsbad, CA Research Associate II/ Senior Research Associate, Core Antisense Research Master’s degree preferred in biochemistry, molecular biology or cell biology, or a B.S. Exp: MS: 0+ years; BS: >1-2 years |
We are seeking a highly qualified and motivated individual to perform basic research to increase our understand on how ASOs target RNA to modulate the expression of genes. The position offers the opportunity to do groundbreaking science and make discoveries that will create the next generation of ASO medicines. The selected candidate will become an integral part of an interdisciplinary and energetic team of scientists in the Ionis Core Research group. | 9/6/2023 |
| 4083 | Iovance Biotherapeutics Philadelphia, PA Aseptic Processing Tech - 2nd Shift [Contract to Hire] B.S. degree in biology, biochemistry, bioengineering, or related technical field. Exp: 0-2 years |
Iovance Biotherapeutics is seeking an Aseptic Processing Techician to join the team at 700 Spring Garden St, Philadelphia, PA.Co-located at the American Red Cross Penn Jersey Region, this Iovance facility produces a critical raw material used in the company’s TIL process. As an Aseptic Processing Technician, you will focus on the documentation for our processes. The ideal candidate will have a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. | 9/6/2023 |
| 4084 | Iovance Biotherapeutics Philadelphia, PA Aseptic Processing Technician [Contract to Hire] B.S. degree in biology, biochemistry, bioengineering, or related technical field. Exp: 0-2 years |
As an Aseptic Processing Technician, you will focus on the documentation for our processes. The ideal candidate will have a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. Iovance Biotherapeutics is seeking an Aseptic Processing Technician (contract-to-hire) to join the team at 700 Spring Garden St, Philadelphia, PA. Co-located at the American Red Cross Penn Jersey Region, this Iovance facility produces a critical raw material used in the company’s TIL process. The critical raw material is processed from leukapheresis units and frozen. Processing is performed in an ISO 7 cleanroom within an ISO 5 biological safety cabinet. | 9/6/2023 |
| 4085 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst, Environmental Monitoring - 2nd Shift [Contract to Hire] Bachelor’s degree in a relevant discipline (biological sciences or equivalent). Exp: one (1) year |
Iovance Biotherapeutics is seeking a Quality Control Analyst to join the team at 700 Spring Garden St, Philadelphia, PA.Co-located at the American Red Cross Penn Jersey Region, this Iovance facility produces a critical raw material used in the company’s TIL process. The critical raw material is processed from leukapheresis units and frozen. The QC Analyst will support quality control environmental monitoring operations at Iovance’s. The quality control environmental monitoring programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, compressed gas monitoring, and/or sterility techniques. | 9/6/2023 |
| 4086 | Cambridge Isotope Laboratories Xenia, OH Quality Assurance Associate Bachelor’s Degree in chemistry or related science preferred. Exp: 0-2 years |
Cambridge Isotope Separations (CIS) is searching for a GMP Quality Assurance (QA) Associate located in Xenia, Ohio. Cambridge Isotope Laboratories (CIL) and CIS are the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. Under general supervision, the primary responsibility of the QA Associate is to work as a team member to ensure and maintain the Company’s cGMP (Current Good Manufacturing Practices) compliance.Cambridge Isotope Separations (CIS) is searching for a GMP Quality Assurance (QA) Associate located in Xenia, Ohio. | 9/7/2023 |
| 4087 | Cambridge Isotope Laboratories Tewksbury, MA Quality Control Analyst I BS or MS degree in Chemistry or other relevant science degree. Exp: One or more years |
Cambridge Isotope Laboratories, Inc. has an outstanding opportunity to join our GMP Quality Control team as a Quality Control Analyst I based onsite in our Tewksbury, MA headquarters. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control Analyst I is responsible for conducting routine analysis of GMP/ISO materials including: Raw materials, in-process and finished products under general supervision and in accordance with standard operating procedures (SOPs). The analyst will compile data for documentation of test procedures and prepare reports. They also calibrate and maintain lab equipment and participate in general upkeep of the laboratory.Cambridge Isotope Laboratories, Inc. has an outstanding opportunity to join our GMP Quality Control team as a Quality Control Analyst I based onsite in our Tewksbury, MA headquarters. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control Analyst I is responsible for conducting routine analysis of GMP/ISO materials including: Raw materials, in-process and finished products under general supervision and in accordance with standard operating procedures (SOPs). The analyst will compile data for documentation of test procedures and prepare reports. They also calibrate and maintain lab equipment and participate in general upkeep of the laboratory. | 9/7/2023 |
| 4088 | Cambridge Isotope Laboratories Andover, MA Chemist MS in Chemistry Exp: 1-3 years |
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Chemist based onsite in our Andover, MA location. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. Under the supervision of a group leader or supervisor, the Chemist will work alongside an experienced scientist executing syntheses of isotopically labeled (13C, 15N, 18O and D isotopes) targets utilizing highly detailed SOPs and procedures. | 9/7/2023 |
| 4089 | Fresenius Kabi Melrose Park & Chicago, IL Associate Scientist (Nights) BS/BA degree in Science or related field. Exp: 0+ years |
The Associate Scientist will be responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Reports testing results and documents in compliance with cGMP and GLP standards. Provides support to Scientist, Lead Scientist, and Supervisor. Prepares media, reagents, sanitizing solutions and equipment for use in testing. | 9/7/2023 |
| 4090 | Fresenius Kabi Melrose Park & Chicago, IL Scientist I B.S. degree in Chemistry or Biology, or equivalent physical science. Exp: 1 year |
Responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Independently executes protocols, verifications, method transfers in support of senior level personnel. Directs and provides guidance to associate scientists. | 9/7/2023 |
| 4091 | Fresenius Kabi Melrose Park & Chicago, IL Associate Scientist (Nights) BS/BA degree in Science or related field. Exp: 0+ years |
The Associate Scientist will be responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Reports testing results and documents in compliance with cGMP and GLP standards. Provides support to Scientist, Lead Scientist, and Supervisor. Prepares media, reagents, sanitizing solutions and equipment for use in testing. | 9/7/2023 |
| 4092 | Fresenius Kabi Melrose Park & Chicago, IL Associate Scientist B.S. in Chemistry, Biology or related physical science. Exp: 1+ years |
The Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 9/7/2023 |
| 4093 | Fresenius Kabi Grand Island , NY SCIENTIST (Chemistry) - 3rd Shift B.S. in Chemistry, Biology, or related physical science. Exp: 1-4 years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 9/7/2023 |
| 4094 | Fresenius Kabi Grand Island , NY ASSOCIATE SCIENTIST - 2nd Shift Chemistry B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 9/7/2023 |
| 4095 | Fresenius Kabi Grand Island , NY ASSOCIATE SCIENTIST - 1st Shift Chemistry B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 9/7/2023 |
| 4096 | Janssen Pharmaceuticals Brisbane, CA Associate Scientist, Oligonucleotide Biology - RNA, Gene Therapy and Delivery M.S. Exp: 1 year |
We are seeking an accomplished and curious Associate Scientist to join our Oligonucleotide Biology team in the discovery of targeted oligonucleotide therapeutics. At our San Francisco Bay Campus in Brisbane, the Associate Scientist will help develop and implement diverse in vivo and in vitro assays, while collaborating with highly motivated teams to optimize siRNA/mRNA therapeutics. A strong candidate will have expertise in in vivo and ex vivo techniques, cell-based assays, and excellent interpersonal talents. | 9/19/2023 |
| 4097 | Janssen Pharmaceuticals Spring House, PA PK Analyst - Associate Scientist I/II M.S. Exp: 1-3 years |
Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies is recruiting for a PK Analyst to join the team as an Associate Scientist I/II located in Spring House, PA. This is a scientific position within the nonclinical pharmacokinetic (PK) assay development and bioanalysis team within the Development PK group of the Bioanalytical Discovery and Development Sciences (BDDS) of Janssen R&D. Our team develops, validates, and conducts bioanalytical studies related to large molecule biotherapeutic drugs in a highly regulated environment (GLP and GCP regulations). We work across all therapeutic areas within Johnson & Johnson, spanning nonclinical studies to post-market clinical development | 9/19/2023 |
| 4098 | Janssen Pharmaceuticals Danvers, MA Product Development Engineer I, Surgery BS in Mechanical Engineering or directly related scientific discipline, MS Preferred. Exp: 1-3 years |
Abiomed, part of Johnson & Johnson MedTech, is recruiting for a Product Development Engineer located in Danvers, MA. The ideal Product Development candidate will be goal, data-driven, detail oriented; and experienced in the medical industry. The Product Development Engineer will lead complex technical tasks and engineering process improvements, collaborate with senior and junior staff, develop new products, and provide engineering support for existing products. | 9/19/2023 |
| 4099 | J-Star Cranbury, NJ Research Scientist Master’s degree in Chemistry, Chemical Engineering, or Materials Science and Engineering. Exp: one year |
Research Scientist wanted for J-Star Research Inc in Cranbury, New Jersey. Must have knowledge of FDA regulations, Polymorph characterization, crystallization, distillation, quantitative analysis, Thermo-Property test, HPLC, UPLC, IC, LC-MS, Methodology Development, and column chromatography. Job duties to be performed: Perform Active Pharmaceutical Ingredient (API) crystallization process in compliance with cGMP and FDA regulations, utilizing polymorph and physical properties analytical tools, including spectroscopy, microstructure monitoring, separation, and solvent selection. Conduct crystallization process development by conducting studies involving materials engineering and experimental design; Generate materials for pharmaceutical research. Participate in the scale-up development of enabling technology and experiments to facilitate the co-processing and development of API. Conduct routine stability, performance, and evaluation studies for solid state characterization and pre-formulation support using Polymorph characterization. Conduct early drug crystallization process development for high potency compounds and controlled substances. Purify pharmaceutical compounds using column chromatography, crystallization, trituration, extraction, and distillation. | 9/8/2023 |
| 4100 | J-Star Cranbury, NJ Senior Research Chemist Master’s degree in Chemistry. Exp: one year |
Senior Research Chemist wanted for J-Star Research Inc in Cranbury, New Jersey. Must have knowledge of synthetic organic chemistry, methodology development, reaction optimization, quantitative assays, HPLC, LC/MS, NMR, IR, purification techniques including column chromatography, crystallization, and distillation. Job duties to be performed: Plan and execute process chemistry R&D proposals for pharmaceutical and biotechnology projects in compliance with FDA regulations. Design synthetic routes for the preparation of small molecule pharmaceuticals with principles of synthetic organic chemistry. Develop and optimize chemical methodologies and processes to synthesize active pharmaceutical ingredients (API) and chemical intermediates utilizing reaction route scouting, and design of experiments (DoE). Scale up the manufacturing process in non-GMP and cGMP kilolabs with operation of the corresponding process equipment. Collaborate in a cross functional team with QA, QC and engineers to support the cGMP production. Purify pharmaceutical compounds using column chromatography, crystallization, and distillation.Senior Research Chemist wanted for J-Star Research Inc in Cranbury, New Jersey. Must have knowledge of synthetic organic chemistry, methodology development, reaction optimization, quantitative assays, HPLC, LC/MS, NMR, IR, purification techniques including column chromatography, crystallization, and distillation. Job duties to be performed: | 9/8/2023 |
| 4101 | Jubilant HollisterStier Spokane, WA Scientist I-II-III, QC Bachelor’s Degree in Chemistry, Biology, or related hard science required. Exp: Scientist I: 0 years; Scientist II: + 1 year |
The QC Scientist I/II/III performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw material/product disposition. Essential responsibilities include: Analyze raw materials, in-process, stability and final container products according to established procedures, and as directed by the supervisor. Record and review data in accordance with GxP to meet regulatory requirements and provide information relevant to product disposition. Perform studies to assess product or procedural problems under the direction of the supervisor. Assist in other forms of troubleshooting/investigations as directed. Prepare reports and assist with document revisions as directed by the Supervisor. | 9/19/2023 |
| 4102 | KBI Biopharma Durham - Hamlin Rd, NC Research Associate I/II BS degree in chemistry, biochemistry, or related area OR MS degree in chemistry, biochemistry or related area. Exp: BS: 0-2+ years'; MS: 0+ years’ |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 9/8/2023 |
| 4103 | KBI Biopharma Durham - National Way, NC Manufacturing Associate I/II-Upstream (Nights) Manufacturing Associate I: Bachelor’s degree in a related scientific or engineering discipline. Exp: MAI: 0-2 years’ |
This position is on a 2-2-3 schedule, with the hours 7p-7a. The Manufacturing Associate I/II – Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II – Upstream must follow the instructions depicted in SR’s, EPR’s, BR’s, SOP’s and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including ‘Right the First Time’ (RFT). Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. The candidate will maintain a sense of ownership of the production processes, manufacturing environment and facility. They will be exposed to cell culture media preparation, shake flask operations, seed expansion, bioreactor setup and operations, cell culture harvest setup and operations, and aseptic technique; as well as to cell culture analytical tools and general biotechnology auxiliary equipment (pumps, sterile tubing welders and sealers, pH/Conductivity/osmolarity meters). Following task execution, the Manufacturing Associate I/II will review the executed production records (SR’s, ERP, and BR’s) to ensure GxP compliance. This position is on a 2-2-3 schedule, with the hours 7p-7a. The Manufacturing Associate I/II – Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. | 9/8/2023 |
| 4104 | KBI Biopharma Boulder, CO Manufacturing Associate I/II (Nights) Bachelor’s degree. Exp: 0-5 years |
This position will be on a 4-3 night shift schedule. The hours are 7:00 pm to 7:00 am. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels | 9/8/2023 |
| 4105 | KBI Biopharma Durham - Hamlin Rd, NC Manufacturing Associate I/II-Upstream\ Manufacturing Associate I: Bachelor’s degree in a related scientific or engineering discipline. Exp: 0-2 years’ |
This position is on a 2-2-3 shift, 7a-7p. The Manufacturing Associate I/II – Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II – Upstream must follow the instructions depicted in SR’s, EPR’s, BR’s, SOP’s and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including ‘Right the First Time’ (RFT). Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. | 9/8/2023 |
| 4106 | KBI Biopharma Boulder, CO Manufacturing Associate I/II Bachelor’s degree. Exp: 0-5 years |
This position will be on a 4-3 day shift schedule. The hours are 7 am to 7 pm. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels | 9/8/2023 |
| 4107 | KBI Biopharma Durham - Hamlin Rd, NC Research Associate II MS degree in chemistry, biochemistry or related area. Exp: 0+ years’ |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 9/8/2023 |
| 4108 | KBI Biopharma Durham - Hamlin Rd, NC Manufacturing Associate I/II Upstream (Nights) Manufacturing Associate I- Bachelor’s degree in a related scientific or engineering discipline. Exp: 0-2 years’ |
This position operates on a 2-2-3 schedule with the hours of 7:00 pm - 7:30 am. The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment. The Manufacturing Associate will be responsible for upstream unit operations (seed expansion, bioreactor operations, cell culture harvest). The Manufacturing Associate will have a working knowledge of upstream processing equipment (incubators, biosafety cabinets, bioreactors, cell counters, blood gas analyzers, metabolite testing equipment). Additionally, the manufacturing associate will have knowledge of general bioprocessing equipment such as filters, filter integrity testers, balances, pumps, pH/conductivity meters, and disposable technologies (disposable bags, sterile tubing welders, tubing sealers). Following task execution, the Manufacturing Associate will review the executed production records and logbooks to ensure GxP compliance. | 9/8/2023 |
| 4109 | Khloris Biosciences San Jose, CA Cell Therapy Manufacturing Technician B.S. degree in biology, biochemistry, bioengineering, or related technical field. Exp: 0-5 years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated cell therapy manufacturing technician to join our team. The selected candidate will work closely with lead manufacturing technicians, scientists, participate in project and team meeting, and work in a multidisciplinary environment. The duties of this position will involve supporting a multidisciplinary manufacturing team in developing Khloris cell therapy platforms. The ideal candidate will have hands-on expertise and comprehensive understanding of cell therapy manufacturing processes. | 9/8/2023 |
| 4110 | Khloris Biosciences San Jose, CA Research Associate Positions - Cancer Vaccine B.S. required in appropriate discipline required (e.g., immunology, cell biology, molecular biology). Exp: 1+ years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated research associates to join the cancer vaccine team. The successful candidate(s) will be responsible for supporting cancer vaccine projects on a preclinical level. Prior experience with rodent tumor models and/or in vitro immune assays is preferred. The selected candidate will work closely with other scientists, participate in project teams, and work in a multidisciplinary environment in order to advance projects. | 9/8/2023 |
| 4111 | Lannett Seymour, IN Raw Materials Chemist I BS Degree in Chemistry or related field. Exp: 0+ years |
This position is primarily responsible for the laboratory testing of raw materials and packaging materials or in-process, release and stability samples for commercial drug products. | 9/8/2023 |
| 4112 | Lannett Seymour, IN Raw Materials Chemist I BS Degree in Chemistry or related field. Exp: 0+ years |
This position is primarily responsible for the laboratory testing of raw materials and packaging materials or in-process, release and stability samples for commercial drug products. | 9/8/2023 |
| 4113 | Lannett Seymour, IN Product Chemist I BS Degree in Chemistry or related field. Exp: 0+ years |
This position is primarily responsible for the laboratory testing of in-process, release and stability samples for commercial drug products. | 9/8/2023 |
| 4114 | Lantheus Medical Imaging Billerica, MA Process Engineer 1 Bachelor’s Degree in Engineering or related science oriented discipline. Exp: 1 to 2 years |
An ideal candidate would have strong background in assessing and processing quality events inclusive of deviations, CAPA plans and actions, and investigations. Be able to use project management skills to organize and lead cross functional teams through data-based decision making for root cause investigations, technical transfers, or project improvements. Support larger projects collaborating across multiple teams. Strong partnership skills to build and maintain relationships. | 9/8/2023 |
| 4115 | Legend Biotech Raritan, NJ QC Analyst Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required. Exp: 1 years |
The QC Analyst, CAR-T Manufacturing is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. | 9/19/2023 |
| 4116 | Legend Biotech Raritan, NJ QC Analyst (3rd shift) Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required. Exp: 1 years |
The QC Analyst, CAR-T Manufacturing is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. | 9/19/2023 |
| 4117 | Galatea Surgical Sumter, SC Quality Engineer II (Onsite) MSc. Degree Exp: 1 years |
BD is seeking a Quality Engineer II to join the team at our medical device manufacturing site in Sumter, SC. As a Quality Engineer II, you'll play an integral role in maintaining compliance with ISO and FDA guidelines while collaborating with local, US-based and international resources. You'll be responsible for building and implementing strategic quality plans and regulatory compliant operating procedures that support routine validation, as well as expansion and upgrade projects. If you're passionate about quality and are looking for a challenging and rewarding career, we want to hear from you! | 8/29/2023 |
| 4118 | Global Blood Therapeutics Kalamazoo, MI QC Laboratory Analyst II (2nd Shift) Bachelor´s degree in Chemistry, Biochemistry or related science degree Exp: 0-1 years |
This position is for a testing analyst in the Kalamazoo QO DP Laboratory working on second shift (3:00PM-11:30PM). Opportunity for schedule flexibility exists as the Laboratory supports business and customer needs on weekends and holidays. Technologies employed in the Rapid Turn Laboratory include HPLC, GC, IC, Titrations, Karl Fisher, UV, FTIR, SG, RI, LOD, and general analytical procedures. | 8/29/2023 |
| 4119 | Global Blood Therapeutics Cambridge, MA Senior Associate Scientist- BMD Biotherapeutic Expression and Purification MS in Chemistry, Biochemistry, Biology, Biomedical Sciences, or a related discipline Exp: 0-2 years |
Pfizer's BioMedicine Design (BMD) is seeking a highly motivated Biochemist/Molecular Biologist to join the Biotherapeutic Expression and Purification group (BEP) in Cambridge, MA. The qualified candidate will play an essential role in a dynamic DNA production and protein expression research laboratory. This group provides non-GMP transient protein lead production support across Pfizer's diverse biotherapeutic discovery portfolio, meeting the in-vitro and in-vivo needs of Pfizer’s research units and their pre-clinical therapeutic programs. The BEP group is looking for a successful candidate who can provide DNA production support for protein expression and purification activities. The ideal candidate is expected to have a strong background in molecular biology techniques, as well as experience in nucleic acid production and analysis. The selected individual will cultivate bacterial cultures and perform large-scale DNA production activities, following standardized protocols. They will be a key contributor to the scientific team responsible for protein expression and purification. | 8/29/2023 |
| 4120 | Global Blood Therapeutics Andover, MA Production Engineer I Bachelor's degree Exp: 1-2 years |
Provide engineering and technical support related to the installation, startup/commissioning, testing, and qualification, sustained operation and maintenance of process and automated equipment and systems within a biopharmaceutical clinical manufacturing facility, as well as commercial/ clinical changeover and tech transfer activities. This may include startup of production equipment such as bioreactors, ultrafiltration skids, Clean – In – Place (CIP) skids, and other support equipment. | 8/29/2023 |
| 4121 | Global Blood Therapeutics Andover, MA Quality Engineer II Bachelor's degree Exp: 0+ years |
You will have knowledge of process equipment and systems and manufacturing operations with the primary responsibility to execute process and equipment operation activities during manufacturing operations. Due to your expertise in the manufacturing domain, you may participate in training for operational qualifications and assist the Team Lead or other team members as needed. You will conduct all activities in accordance with Company policies and standard operating procedures, Pfizer Values, and global regulatory guidelines, environmental guidelines etc. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. | 8/29/2023 |
| 4122 | Global Blood Therapeutics Andover, MA QC Scientist II Bachelor's degree Exp: 0+ years |
You will be a member of Pfizer’s dedicated and highly effective Quality Control Microbiology team. You will be responsible for analyzing microbiological products to support our quality programs. Your contribution to the QC Micro team will help Pfizer provide safe drugs to patients. As a QC Scientist II, your experience in applying knowledge of principles, concepts, and practices of the discipline will make you a critical member of the team. Your skill and knowledge will help in making decisions that require choosing among limited options. Your being proactive in team discussions will help in creating an environment of collaboration. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. | 8/30/2023 |
| 4123 | Global Blood Therapeutics Andover, MA Tech Transfer Engineer I Bachelor's degree Exp: 0+ years |
Provide engineering support related to the evaluation, technology transfer, startup, and qualification of new and existing equipment, facilities, and utilities in support of existing product campaigns and new product introduction. Engineering support will include basic equipment and automation troubleshooting and project execution. This may include production equipment such as bioreactors, ultrafiltration skids, Clean – In – Place (CIP) skids, chromatography skids, and other support equipment. | 8/30/2023 |
| 4124 | Global Blood Therapeutics Andover, MA QA Specialist III Masters Exp: 1+ years |
As a QA Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. | 8/30/2023 |
| 4125 | Genentech Hillsboro, OR Manufacturing Engineer (Cell & Gene Therapy) Bachelor’s degree in cellular or molecular biology or engineering preferred. Exp: 1 year |
Genentech is offering an exciting opportunity for the right individual to join Genentech’s Hillsboro Individualized Therapies (HIT) team, working to bring new medical advancements from development stages to commercial manufacturing. This is an exciting opportunity to work closely with emerging technology including but not limited to individualized DNA/RNA therapies, Cell therapies, and Stem Cell therapies. This is the start-up headquarters for Genentech’s individualized and cell therapies division where we will establish the industry standard. As a member of the team you would be responsible for supporting multi-phase technology transfers and production. | 8/31/2023 |
| 4126 | Genentech Hillsboro, OR Manufacturing Asset Engineer I, HTO (Two Year Term) B.S or higher in Mechanical Engineering, Electrical, Chemical, Biochemical, or related discipline. Exp: 1-2 years’ |
The Asset Engineer is responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as the equipment owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Asset Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 8/31/2023 |
| 4127 | Genentech Oceanside, CA Manufacturing Technical Specialist II/ Engineer I Bachelor's or Master's degree in Engineering or Life Sciences. Exp: 0-4 years |
Responsible for supporting operations in the Oceanside Pilot Plant and Process Engineering Purification/Analytical Lab. Deliverables include but are not limited to: HPLC-based analytics, rapid bioburden/endotoxin, lab scale and pilot scale chromatography, UFDF operations, buffer prep, column packing, equipment maintenance and preparation of technical reports. May commission new equipment, troubleshoot equipment and systems, develop new equipment requirements and operating parameters, and provide factory and site acceptance testing. Provide scientific and technical support to GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. Support process validation through large and small-scale studies, protocol and report preparation, validation sampling, and sample shipments. | 8/31/2023 |
| 4128 | Genentech South San Francisco, CA Technical Development Scientist - Protein Analytical Chemistry BS or MS in biological or chemical sciences, or related disciplines. Exp: 0 to 2+ years |
We are seeking a highly motivated individual to join the department of Protein Analytical Chemistry (PAC) (within PTDU) as a Technical Development Scientist. A successful candidate will be expected to work hands-on in the laboratory to generate analytical data in support of the pipeline and technical development projects. This will include analytical characterization and testing as well as development and execution of analytical methods. The candidate may also collaborate with cross functional colleagues and contribute to manufacturing process development and clinical trial and commercialization-enabling regulatory filings (e.g. BLAs and INDs). This candidate is expected to be a good lab citizen, following all environmental health and safety guidelines and maintaining lab space and instruments in good working order. The individual will maintain excellent documentation of all work, including electronic laboratory notebooks, and will author technical reports. Additionally, the individual will be responsible for presenting experimental results to technical development teams, the PAC department, and other stakeholders on a regular basis. Candidates applying should be passionate about science, exceptionally productive, data-driven and should enjoy the challenges associated with complex problem-solving. Candidates must be highly self-motivated and willing to work independently or as a part of multi-disciplinary teams to ensure the delivery of Genentech’s protein pharmaceutical pipeline. | 8/31/2023 |
| 4129 | Genentech Oceanside, CA Bioprocess Manufacturing Technician (Contract) Preferred - Degree in Life Sciences/Engineering, Associate’s or Biotech certificate from approved program. Exp: 0+ years |
As a Bioprocess Manufacturing Technician, you will be responsible for producing medicine in a highly automated and controlled environment. Each product has a specific recipe; you will follow this recipe, along with the standard operating procedures, to operate the production equipment across various areas, including raw material dispensing/aliquoting, cell culture and purification. You will maintain records and follow all the steps necessary to comply with regulatory requirements within a current Good Manufacturing Practices (cGMP) environment. This is a contract role with the possibility of conversion to a permanent employee position | 8/31/2023 |
| 4130 | Genentech South San Francisco, CA Validation Engineer (Contractor) B.S. degree in Science or Engineering. Exp: 1-2 years |
Genentech's Device Development team is searching for a Validation Engineer to assist, lead, and execute validation activities (e.g., equipment qualification, computer system validation) and manage discrepancies and changes to Qualified/Validated systems. The candidate should have knowledge in Laboratory equipment qualification & validation process, data integrity (CFR Part 11 Compliance) implementation, cGMP documentation, Change Management, and operational maintenance of Laboratory equipment.Genentech's Device Development team is searching for a Validation Engineer to assist, lead, and execute validation activities (e.g., equipment qualification, computer system validation) and manage discrepancies and changes to Qualified/Validated systems. | 8/31/2023 |
| 4131 | GenWay Biotech San Diego, CA Research Associate I/II – Molecular Biology B.S. or M.S. in life science or related subject. Exp: 1+ year |
Aviva Systems Biology is a fast paced, mid stage life sciences research tools company located in San Diego, CA. We commercialize life science tools and reagents for research, drug discovery, and diagnostics. | 9/1/2023 |
| 4132 | GenWay Biotech San Diego, CA Manufacturing Associate I/II B.S. or M.S. in life science or related subject. Exp: 1+ year |
The Manufacturing Associate will assist in the production of recombinant proteins and other biological products under GMP guidelines. Manufacturing team members to develop products in support of the company’s growth strategy. This is a highly collaborative role where you will directly impact the company’s revenue growth. The Manufacturing Associate works as part of a multidisciplinary team performing standard molecular biology techniques, protein purification and analysis, and cell culture maintenance. Clear communication skills, careful execution with attention to details, and excellent record keeping are a must. The ideal candidate will thrive in a fast-paced, dynamic environment as a part of a highly focused team of motivated scientists. | 9/1/2023 |
| 4133 | GigaGen San Carlos, CA Senior Research Associate, Analytical/Assays Master’s degree in Chemistry, Life Sciences, or related discipline. Exp: 1 year |
GigaGen, a subsidiary of Grifols, seeks a talented, highly motivated Senior Research Associate to support the analytical and functional analysis of our diverse antibody therapeutics pipeline, including the development and implementation of analytical and functional assays for characterizing antibodies and antibody derivatives. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 9/1/2023 |
| 4134 | GigaGen San Carlos, CA Research Associate Bachelor’s degree in Life Sciences or related discipline. Exp: 1 year |
GigaGen, a subsidiary of Grifols, seeks a talented, highly motivated Research Associate to support our diverse antibody therapeutics pipeline. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 9/1/2023 |
| 4135 | Glaukos San Clemente, CA Microbiologist Bachelor's Degree in Microbiology, Biology, or Biochemistry. Exp: 1-2 years |
The Microbiologist/QA Engineer-Pharma and Medical Devices - position will be based in San Clemente, CA and will directly support the manufacture of innovative ocular medical devices and pharmaceuticals. This role includes ensuring proper execution of Environmental Monitoring tasks, reviewing routine and event-based environmental related project protocols, validations, reports, and data assessment. The candidate will assist with EM testing, bioburden testing, growth promotion and other microbiological testing within the lab. The candidate will coordinate and monitor EM related activities to ensure quality and on time completion of EM related tasks. The candidate is also expected to work collaboratively with internal cross-functional groups - R&D, Operations, Facilities - and with external contract vendors. | 9/1/2023 |
| 4136 | Glaukos San Clemente, CA Engineer I/II (Pharma Operations) Bachelor’s degree in Engineering or Science. Exp: 6 months - 2 years |
Responsible for manufacturing of development, pilot, clinical, verification/validation, stability study campaigns, and commercial production whether internal or at CMO (hands-on as needed). | 9/1/2023 |
| 4137 | Grand River Aseptic Manufacturing Grand Rapids , MI Aseptic Manufacturing Associate (Weekend Shift) Bachelor’s degree Exp: 0-1 year |
The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or management. Weekend shift hours are Friday, Saturday, Sunday, 12-hour shifts (either 6am-6pm, or 6pm-6am). Weekend shift differentials and paid breaks! | 9/1/2023 |
| 4138 | Grand River Aseptic Manufacturing Grand Rapids , MI Aseptic Manufacturing Associate (2nd and 3rd shifts) Bachelor’s degree Exp: 0-1 year |
The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. | 9/1/2023 |
| 4139 | Grand River Aseptic Manufacturing Grand Rapids , MI QC Chemist (3rd Shift) Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology). Exp: 1-3 years |
The Quality Control Chemist is responsible for supporting quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 9/1/2023 |
| 4140 | Grifols Clayton, NC Assistant/Associate Biologist BS/BA degree in a life science field, medical technology, or related curriculum is required. Exp: 6 mos+ years |
The incumbent is responsible for performing complex laboratory analysis of plasma and plasma products in a GMP laboratory. Responsibilities include sample accessioning, sample preparation, reagent preparation, testing, result calculation, as well as quality control of assays and equipment. The incumbent will also support assay validation, method transfer, reagent and control qualification, and laboratory maintenance activities as assigned. Must be comfortable working with infectious material on a daily basis. Person must be able to work in a biological safety cabinet and comfortable working with a microscope for several hours at a time. Candidates for the position must be proficient with using micropipettes and serological pipettes while making dilutions and serial dilutions. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform their share of cleaning duties and housekeeping. This position is responsible for performing bioburden and endotoxin testing of in-process product samples and raw materials to support plasma production processes, including process and equipment activities. The Quality Control Sterility & Microbiology department must maintain adequate staffing to support all production operations 24 hours per day, 7 days a week. In addition to in-process product monitoring, this position may also assist with environmental monitoring of production and testing areas. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site production processes and production areas remain in a state of control. | 9/1/2023 |
| 4141 | Grifols Clayton, NC Assistant/Associate Biologist BS degree in biology, chemistry, or related field. Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in B300 and SFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems. remain in a state of control. Current production levels require that multiple filling activities can occur during any shift and require EM staff to be available to support these activities in order to avoid production delays. | 9/1/2023 |
| 4142 | Grifols Clayton, NC Assistant Biologist/Associate Biologist BS degree in biology, chemistry, or related field. Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in B300 and SFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems. remain in a state of control. Current production levels require that multiple filling activities can occur during any shift and require EM staff to be available to support these activities in order to avoid production delays | 9/1/2023 |
| 4143 | Grifols Boston, MA Field Service Engineer I Bachelors Degree, Engineering, Technical or related Scientific Discipline. Exp: Entry Level |
The Field Service Engineer will have the primary responsibility of providing the highest quality service and support to Grifols customers at the customer facility and by telephone. This position will be working at customer sites overseeing installations, preventative maintenance, repairs, software and hardware updates. This position will oversee New England, primarily Boston, MA. The ideal individual will have a mechanical or electrical background, have at least 2 years of industry experience working as a Field Service Technician, and previous experience in operating diagnostics equipment in a laboratory environment. | 9/1/2023 |
| 4144 | Grifols Montreal (Canada), CA Automation Engineer M.Sc in Engineering, Automation, Computer, Industrial, Manufacturing or related program. Exp: 1 year |
The Automation Engineer II is a junior level professional who is responsible for using technology to improve and streamline a manufacturing process through automation. Depending on their specific assignment, the incumbent provides automation support for projects or within a specific area, or provides validation support for automation projects. The Automation Engineer II will also integrate into supporting a large scale project. The incumbent is recognized as proficient in her/his field such as specific control systems, instrumentation, process, utilities, or qualification testing. He/she meets customer needs and business goals. In addition, he/she will collaborate with other automation engineers. | 9/1/2023 |
| 4145 | Grifols Clayton, NC Assistant Biologist/Associate Biologist BS degree in biology, chemistry, or related field. Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in B300 and SFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems. remain in a state of control. Current production levels require that multiple filling activities can occur during any shift and require EM staff to be available to support these activities in order to avoid production delays. | 9/1/2023 |
| 4146 | GlaxoSmithKline Marietta, PA Quality Control Technician B.S. in biology, microbiology, chemistry. Exp: six months |
As Quality Control Technician, you will be responsible for collecting environmental monitoring and utility samples, collecting PEMS data, and performing microbiology testing such as Bioburden and plate reading identification. You will also perform data review for Environmental Monitoring or Microbiology data, perform routine laboratory tasks such as safety shower and eyewash testing, BSC cleaning and stocking, level one audits, daily pH meter and balance calibration, etc, and perform tasks associated with ordering laboratory supplies and maintaining laboratory equipment. | 9/1/2023 |
| 4147 | GlaxoSmithKline Rockville, MD Associate QC Chemist BS Degree in Lifesciences field or Master’s degree in Biochemistry or related field. Exp: 1+ years |
GSK is currently looking for an Associate QC Chemist in Rockville, MD. The Associate QC Chemist performs quality control testing, and data review for biopharmaceutical medicine products. | 9/1/2023 |
| 4148 | GlaxoSmithKline Hamilton, MT QC Analyst 2 Bachelor's Degree in a scientific discipline. Exp: 1+ year(s) |
As a QC Analyst 2 you will perform routine QC laboratory activities to support the manufacture and release of products and incoming materials. Understand test equipment and scientific principles of methods within the scope of their responsibility. | 9/1/2023 |
| 4149 | GlaxoSmithKline Rockville, MD Associate Microbiologist BA/BS in Science field. Exp: 1 year |
GSK currently has an opening for an Associate Microbiologist in Rockville, MD. In this role, you’ll be providing routine QC Microbiology laboratory, with the purpose of meeting daily routine requirements as well as achieving goals established by the manager. | 9/1/2023 |
| 4150 | GlaxoSmithKline Cambridge, MA EHS Associate Bachelor’s degree. Exp: 1+ years |
GSK is currently looking for a EHS Associate to join our team in Cambridge, MA. As an Environment, Health, and Safety Specialist, you will be responsible for providing specialized support and expertise to Binney Street staff in office, laboratory, and manufacturing environments. You will develop, coordinate, and implement environmental, health, and safety training programs with policies and procedures to promote and ensure effective EHS operations in the organization. You will monitor environmental, safety, and health regulations to ensure compliance with federal and state regulations. | 9/1/2023 |
| 4151 | Hillrom Round Lake, IL Research Associate I Bachelors degree in a science-related field. Exp: 0-1 years |
The research we do and the products we develop improve outcomes for patients around the world. As a Research Associate I at Baxter, your work contributes directly to making a significant impact on others. We collaborate cross-functionally and lead by influence. Whether guiding a team through a project or leading teams directly, our research and development team is responsible for influencing others to achieve results! Our colleagues within our R&D organization desire to work on products that make a meaningful difference in others' lives. We are motivated by the power of teamwork and are natural leaders who are skilled at influencing others. When you join Baxter as a Research Associate I, you'll use your analytical approach to identify risks and opportunities for innovation quickly. Agile and willing to take action, you stay calm under pressure! | 9/1/2023 |
| 4152 | ICU Medical San Clemente, CA Engineer I, Product Design - (23300846) Bachelor of Science degree from an accredited college or university in Mechanical Engineering or a related field. Master's Degree preferred.? Exp: 0-2 years |
The Product Design Engineer will support the Business Development R&D department. The engineer is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. The key responsibility of this position is to design, develop, and improve ICU’s product portfolio to ensure their efficiency and reliability. The incumbent will be heavily involved with plastics, polymers, molding, medical disposables, plastics engineering, and solid modeling. The R&D Product Engineer will be expected to interface mainly with internal customers and external suppliers on the design and configuration of high-volume disposable medical devices. The position plays a key role in assisting in the development and compliance challenges involved with new medical devices. The position requires the ability to interact with multiple functional groups such as Marketing, Regulatory, Quality, Operations, etc. | 9/1/2023 |
| 4153 | ICU Medical San Clemente, CA Engineer I, Product Design - (23300845) Bachelor of Science degree from an accredited college or university in Mechanical Engineering or a related field. Master's Degree preferred.? Exp: 0-2 years |
The Product Design Engineer will support the Business Development R&D department. The engineer is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. The key responsibility of this position is to design, develop, and improve ICU’s product portfolio to ensure their efficiency and reliability. The incumbent will be heavily involved with plastics, polymers, molding, medical disposables, plastics engineering, and solid modeling. The R&D Product Engineer will be expected to interface mainly with internal customers and external suppliers on the design and configuration of high-volume disposable medical devices. The position plays a key role in assisting in the development and compliance challenges involved with new medical devices. The position requires the ability to interact with multiple functional groups such as Marketing, Regulatory, Quality, Operations, etc. | 9/1/2023 |
| 4154 | Integrated DNA Technologies SE Bothell, WA Manufacturing Laboratory Technician Bachelor' degree Exp: 0 years' |
The Manufacturing Laboratory Technician is responsible for supporting manufacturing of synthetic oligonucleotides under a cGMP environment for use in Cepheid in-vitro diagnostic products. The position is part of the Oligo Production team and is located in Bothell, WA. At Cepheid, our vision is to be the leading provider in seamlessly connected diagnostic solutions. | 9/1/2023 |
| 4155 | Integrated DNA Technologies SE Bothell, WA Oligonucleotide Manufacturing Chemist BS in Chemistry, Biochemistry preferred. Exp: 0-2 years |
The Oligonucleotide Manufacturing Chemist supports manufacturing of synthetic oligonucleotides under a cGMP environment for use in Cepheid in-vitro diagnostic products. The Chemist will use scientific knowledge and understanding to execute and document standard operating procedures to ensure successful manufacturing and on time delivery of Oligonucleotides. They will contribute to the successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization and support processes to ensure performance within expected parameters. This position is part of the Oligonucleotide Manufacturing team and will be located onsite in Bothell, Washington facilities. | 9/1/2023 |
| 4156 | Illumina San Diego, CA Engineer 1 - Fluidics Systems B.S. or above in Mechanical Engineering, Bioengineering, Systems Engineering, Applied Physics or related field. Exp: 0 to 2 years |
The Engineer 1 role in Fluidic Systems is part of the Illumina product development team creating new industry-leading genetic analysis platforms for life sciences and clinical markets. You will work in a very interdisciplinary team environment to develop industry-leading genetic analysis instrumentation and device products. Primary responsibilities of this position include design and evaluation of fluidic and microfluidics devices and components in both instruments and consumables, functional spec characterization as it pertains to system-level performance and workflows, critical parameter studies to drive high reliability and robustness, and failure analysis to root cause, mitigation, and permanent correction. You will be responsible for supporting the design, test, and manufacturing transfer of fluidic components, consumables and sub-systems, with a hands-on approach to troubleshooting. This candidate should possess strong organizational and communication skills to facilitate successful product development across instrument, consumables, chemistry, and software teams. | 9/1/2023 |
| 4157 | Cytovance Biologics Oklahoma City, OK QC Stability Associate B.S. in Life Sciences/Chemistry Exp: 1+ Years |
The Stability Associate will participate in the QC Stability Study Program activities which includes designing and drafting stability study protocols according to ICH guidance for drug substance, drug product and reference standard, participate in range of quality control analytical activities such as analytical assay performance, and transfer of standard protein characterization methods. Duties will be carried out in accordance with quality standards and procedures set by the company and applicable government agencies | 8/21/2023 |
| 4158 | Day Zero Diagnostics Boston, MA Associate Bioinformatician Bachelor’s or master’s degree in Computer Science, Bioinformatics, Computational Biology, or a related quantitative field. Exp: Entry Level |
The Associate Bioinformatician will join our Computational Biology team and report directly to a Research Scientist. This person will provide bioinformatics support on R&D projects relating to microbial genomics. Potential projects may include developing bioinformatics pipelines for deployment in MicrohmDB®, our large-scale database of whole genome sequencing data and resistance profiles, or performing bioinformatics analyses that inform updates to Keynome® gAST, our machine learning algorithm used for genomic Antibiotic Susceptibility Testing. This person will have opportunities to work with a world-class database of pathogen genomes and to learn cutting-edge bioinformatics techniques. A strong candidate for this position will be both excited to contribute their knowledge and eager to broaden their skillset to new areas. | 8/21/2023 |
| 4159 | Day Zero Diagnostics Boston, MA Laboratory Research Associate, Sequencing Bachelor's Degree in molecular biology, biochemistry or microbiology. Exp: Entry Level |
PRIMARY RESPONSIBILITIES Perform and assist with sample processing toward diagnostic workflows Strictly follow all lab procedures for specimen handling, processing, and reporting Maintain meticulous documentation of experimental outcomes and observations Work closely with Research Scientists and Associates, and maintain close communication with direct supervisor Repetitive workflows are a frequent occurrence | 8/21/2023 |
| 4160 | DiaCarta Pleasanton, CA Research Associate Sc. degree in molecular biology or a related field. Exp: 0-1 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 8/21/2023 |
| 4161 | DiCE Molecules South San Francisco, CA Research Associate/Sr. Research Associate Medicinal Chemistry BS or MS in organic chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based synthetic chemistry Research Associate / Senior Research Associate to join our medicinal chemistry team. This individual will be a key contributor to the synthesis of intermediates and final compounds within the goals of developing treatments for inflammatory diseases. Must have legal right to work in US. | 8/21/2023 |
| 4162 | DiscGenics Salt Lake City, UT Manufacturing Associate Bachelor’s degree in related field. Exp: 1+ years |
As DiscGenics prepares to commercialize IDCT, the Manufacturing Associate will be a critical role to execute the daily functions of making IDCT from engineering through commercial production. This role interacts with all levels of the organization in a collaborative and positive way with colleagues to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. | 8/22/2023 |
| 4163 | Distributed Bio Mattawan, MI Research Technician - Second Shift Operations *$1,000 sign on bonus *$20/hr starting wage 1 Bachelor’s/Master’s Exp: 0+ years |
We are seeking a Research Technician for our Second Shift Operations at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 8/22/2023 |
| 4164 | Distributed Bio Durham, NC Research Technician I Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline. Exp: 1+ years |
We are seeking a Research Technician 1 for our Discovery site located Durham. | 8/22/2023 |
| 4165 | Distributed Bio Mattawan, MI Research Analyst I- Formulations Bachelor’s/Master’s degree in a relevant field. Exp: 0+ years |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. | 8/22/2023 |
| 4166 | Distributed Bio Durham, NC Research Technician I Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline. Exp: 1+ years |
We are seeking a Research Technician I for our Discovery site located Durham. | 8/22/2023 |
| 4167 | Distributed Bio Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician 1 at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 8/22/2023 |
| 4168 | Distributed Bio Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician 1 at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 8/22/2023 |
| 4169 | Distributed Bio Mattawan, MI Research Analyst 1 - Discovery Bioanalytical BS/BA in relevant field. Exp: 0-2 years |
We are seeking a Research Analyst 1 for our Discovery Bioanalytical Chemistry Team in Mattawan MI. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 8/22/2023 |
| 4170 | Earli Redwood City, CA Temporary Research Associate or Senior Research Associate, Cell Biology BS or MS degree in Life Sciences or Cell Biology or Immunology. Exp: 1-2 years |
Earli, Inc. is currently seeking a dynamic Senior/Research Associate who is inspired to change the world by pushing the scientific envelope. | 8/22/2023 |
| 4171 | Earli Redwood City, CA Temporary Senior Research Associate - LNP Formulation Bachelors or Masters degree in biology, chemistry, or life sciences (STEM) Exp: 0 – 1 year |
Earli is seeking a highly motivated and ambitious Senior Research Associate interested in pursuing a career in biotech. The candidate will gain hands-on experience in lipid nanoparticle formulation and characterization, learn about LNP design, and be part of a supportive team. The main responsibility for this role is to provide small scale formulations for in vivo studies. The candidate should have basic hands-on experience working in a biology or chemistry lab and be a highly responsible and reliable individual. The candidate should be comfortable working in a fast-paced environment and excited to contribute to Earli’s mission. | 8/22/2023 |
| 4172 | Exponential Business & Technologies Eden Prairie, MN Nano Analytical and Testing Lab Technician BE or BS degree in Materials Science and Engineering, Mechanical Engineering, Physics, Chemistry or related disciplines. Exp: One to two years |
Ebatco is seeking an energetic, self-disciplined, customer service oriented technical person to join its Nano Analytical and Testing Laboratory (NAT Lab). As a technical member of the NAT Lab team, the technician performs contract lab services and instrument demonstrations with appropriate levels of support and supervision, operates advanced nano/micro scale scientific instruments, collects testing and measurement data, and writes technical report on experimental results and observations. | 8/22/2023 |
| 4173 | Editas Medicine Waltham, MA Cell Manufacturing Associate - 2259 Bachelor’s degree in Life Sciences/Engineering field. Exp: 0-2 years |
Key Responsibilities & Accountabilities: Perform duties as dictated by standard operating procedures (SOPs) for cellular product manufacturing and under GxP guidelines as directed. Work in a clean room environment while fully gowned following GMP guidelines and using aseptic technique. Work in a Biological Safety Cabinet for open processing operations. Operate instrumentation needed for cell manufacturing. Accurately complete batch record documentation, all appropriate equipment log entries, and GMP documentation. Maintain orderly lab space. Maintain sufficient inventory of supplies and reagents for performance of duties. Clean and maintain laboratory equipment in good working order. Prepare solutions and culture media as appropriate. Work in compliance with all appropriate laboratory regulatory and safety requirements. | 8/22/2023 |
| 4174 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - 12 Hour Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, or other life science discipline. Exp: 0+ years |
$7k sign-on bonus for this position The Associate Production Scientist at MilliporeSigma will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department.$7k sign-on bonus for this position The Associate Production Scientist at MilliporeSigma will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 8/23/2023 |
| 4175 | EMD Serono St. Louis, MO Associate Production Scientist - 2nd Shift Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, Biology or STEM degree. Exp: 1 + years |
MilliporeSigma has an opening at the St. Louis - Broadway site as a 2nd Shift Associate Production Scientist! In this role you will lead the group and assist the Supervisor and other departments to meet the manufacturing department needs. 2nd shift hours are from 2:00pm to 10:30pm Monday-Friday. | 8/23/2023 |
| 4176 | EMD Serono Miamisburg, OH Associate Production Scientist Bachelor’s Degree in Chemistry Exp: 0+ years |
At MilliporeSigma the Associate Production Scientist will manufacture or evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department. He/she will safely perform operations to meet quality expectations ensuring quality throughout the process. The Associate Production Scientist must also complete the volume of work required to achieve group/departmental goals and meet deadlines. Participation in quality audits will be required as needed. In compliance with change control procedures, he/she will also be responsible for improving processes through application of scientific knowledge, experience, and principles. | 8/23/2023 |
| 4177 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - 12 Hour Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, or other life science discipline. Exp: 0+ years |
*$7,000 Sign-On Bonus for 12 hour Night Shifts* Paid after 90 days of employment Your Role: As an Associate Production Scientist at MilliporeSigma, you will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department* | 8/23/2023 |
| 4178 | EMD Serono Rocklin, CA Production Lab Tech 1 Undergraduate Degree in Chemistry, Biochemistry, or other life science discipline Exp: 0+ years |
MilliporeSigma in Rocklin, CA is hiring a Production Lab Tech 1. The position is responsible for all tasks related to Production and Warehouse duties. This individual will work independently with a high level of attention to detail and in accordance with GMP regulations. | 8/23/2023 |
| 4179 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, Biochemistry or other life science discipline Exp: 0+ years |
*$7,000 Sign-On Bonus for this 12 hour Night Shift* Paid out after 90 days of employment Your Role: The Associate Production Scientist at MilliporeSigma in Sheboygan Falls, WI, will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 8/23/2023 |
| 4180 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - 3rd Shift Bachelor’s Degree in Chemistry, Chemical Engineering, Biochemistry, or other life science discipline Exp: 0+ years |
The Associate Production Scientist at MilliporeSigma in Sheboygan Falls, WI, will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 8/23/2023 |
| 4181 | Endo Pharmaceuticals Rochester, MI Chemist II (Afternoon Shift) Master’s Degree in chemistry, chemical engineering or related field. Exp: 1+ years’ |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 8/23/2023 |
| 4182 | Endo Pharmaceuticals Rochester, MI Validation Engineer I Bachelor of Science in Engineering or Science discipline preferred Exp: Zero (0) to three (3) years |
The Validation Engineer I evaluates and performs specified validations leading to the accurate and reliable validation of products, processes, equipment, facilities, and systems; assists/performs development of studies/cycles for new processes; helps troubleshoot product problems related to validation; performs testing and documents results for review by site, corporate and government review. Further responsible for providing supporting protocol rationales/justifications for the chosen validation methodology/approach. Participates in programs to achieve departmental objectives. Records and reports results. Notes unusual results and notifies management for evaluation. Assists with writing validation documents. | 8/23/2023 |
| 4183 | Endo Pharmaceuticals Rochester, MI Quality Associate Specialist, Product Release - Midnight Shift BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 8/23/2023 |
| 4184 | Exosome Diagnostics Waltham, MA Medical Laboratory Technologist Bachelor of Science Degree in a chemical, physical or biological science. Exp: six months |
This position is responsible for performing high-complexity CLIA testing in day-to-day operations of the laboratory. | 8/24/2023 |
| 4185 | FORMA Therapeutics Lexington, MA Research Associate - Chemistry Bachelors or Masters in Chemistry or related field. Exp: 1-3 years |
Dicerna Pharmaceuticals is seeking a highly motivated Research Associate with a strong background in synthetic and medicinal chemistry to join the Chemistry Team. The candidate will be responsible for the synthesis of oligonucleotide conjugates, nucleoside analogues, small molecule ligands, and linkers. This position will contribute to the development of novel nucleic acid conjugate platforms and support therapeutic programs in multiple disease areas. The Dicerna research team will provide an exciting learning opportunity and a collaborative and fast-paced research environment. | 8/25/2023 |
| 4186 | FORMA Therapeutics Fremont, CA Engineer I Bachelor Degree within subject matter expertise preferred. Exp: 0- 1+ years’ |
The Engineer I will make significant contributions to the research of life changing medical devices at Novo Nordisk (NN). They leverage their strong background in engineering to perform their individual tasks as well as energetically engaging in collaborative work. The Engineer I will contribute to insert subject matter expertise. They ensure strong progress on research initiatives under the broad direction of more senior engineers and management. | 8/25/2023 |
| 4187 | FORMA Therapeutics West Lebanon, NH Cell Therapy Lab Technician Bachelor’s degree in Cell Biology, Molecular Biology, or a closely related field required. Exp: One (1) year |
This position has the responsibility of working with associates and scientists to execute laboratory scale process development or validation studies in support of manufacturing development, or process troubleshooting, or scale-up. This position is located in West Lebanon, New Hampshire and will require onsite work and collabortation. It is a full time (40 hours per week) position and the standard schedule is Monday-Friday (8am-5pm), with weekends based on business needs. | 8/25/2023 |
| 4188 | FORMA Therapeutics West Lebanon, NH Manufacturing Science and Analytical Technology Associate I Bachelor’s degree or equivalent in Biochemistry, Chemistry, Engineering or a closely related field. Exp: one year |
This position has the responsibility of working with senior level Scientists to execute laboratory scale process development or validation studies in support of process or assay development, or process troubleshooting or scale-up. The scientific knowledge in this position will range from familiarity with details of manufacturing process, process chemistries, development studies and relevant assay methods and instruments. This position will be one of the interfaces between Manufacturing Science and Analytical Technology (MSAT) and Manufacturing or Quality. | 8/25/2023 |
| 4189 | FORMA Therapeutics West Lebanon, NH Manufacturing Technician - Night Shift Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. With the growth of our site, we are seeking night shift support. We offer the following shift schedules that include a 15% shift differential: 7:00pm-7:00am (everyother week has 8-hours built in overtime): Sunday-Tuesday and everyother Saturday Wednesday-Friday and everyother Saturday | 8/25/2023 |
| 4190 | FORMA Therapeutics West Lebanon, NH Manufacturing Technician Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. We offer both day and night shifts positions (schedule below). With the growth of our site, we are seeking night shift support. Day Shift (7:00am-7:00pm) : Sun-Tuesday everyother Wedneday Thur-Saturday everyother Wednesday Night Shift (7:00pm-7:00am- includes 15% shift differential): Sunday-Tuesday everyother Saturday Wednesday-Friday everyother Saturday | 8/25/2023 |
| 4191 | FORMA Therapeutics Clayton, NC Quality Assurance Area Specialist I or II Bachelor’s Degree (or equivalent) required, a scientific discipline preferred. Exp: one (1) year |
This position will reviews manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Will assist in the internal audit program and be a QA presence on the manufacturing floor. | 8/25/2023 |
| 4192 | Fresenius Kabi Melrose Park & Chicago, IL Manufacturing Engineer Bachelor’s degree in Engineering (Electrical, Chemical, Controls, Computer, Mechanical, etc.). Exp: 1-3 years |
The Manufacturing Engineer will use technical expertise in support of daily operations in aseptic filling or formulation by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity. Apply accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyze situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 8/25/2023 |
| 4193 | Fresenius Kabi Melrose Park & Chicago, IL Associate Scientist (Nights) BS/BA degree in Science or related field. Exp: 0+ years |
The Associate Scientist will be responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Reports testing results and documents in compliance with cGMP and GLP standards. Provides support to Scientist, Lead Scientist, and Supervisor. Prepares media, reagents, sanitizing solutions and equipment for use in testing. | 8/25/2023 |
| 4194 | Fresenius Kabi Grand Island, NY SCIENTIST (Chemistry) - 3rd Shift B.S. in Chemistry, Biology, or related physical science. Exp: 1-4 years |
3rd Shift is 10 PM to 6:30 AM, Monday through Friday nights. This position starts between $28.46 - $34.00/hour. A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 8/25/2023 |
| 4195 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 2nd Shift Chemistry B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
This position pays between $22.76 - $23.76/hour. An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 8/25/2023 |
| 4196 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift Chemistry B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 8/25/2023 |
| 4197 | Catalog Boston, MA Mechatronics Engineer BS in Mechatronics, Mechanical, Electrical, or a related engineering field. An advanced degree is a plus. Exp: Entry Level |
We are seeking a dynamic Mechatronics Engineer to join our multidisciplinary team. We are pushing the boundaries of science and technology, and you can help make the difference. This position, while guided by the Mechanical Engineering team, will work closely with Biology and Computer Science groups in our quest to develop next-generation DNA writing technology. We're looking for someone who can turn an idea from a brainstorming session into a proof-of-concept test system through background research, project plan development, custom test equipment design, experimental prototype building, code writing for test automation, and experimental data analysis. | 8/15/2023 |
| 4198 | Catalog Boston, MA Research Associate or Senior Research Associate, DNA Computing BS or MS in biology, molecular biology, biochemistry, or a related discipline. Exp: Entry Level |
We are actively seeking a Research Associate or Senior Research Associate with a solid grounding in molecular biology or chemistry. In this role, you'll be instrumental in helping to build CATALOG's innovative DNA-based data storage and computation platform. You'll collaborate with our dynamic team of computer scientists and biologists, developing novel storage and computing architectures and translating them into scalable chemical operations. Your work will contribute to the optimization of a molecular instruction set that underpins the world’s first DNA storage and computing platform. | 8/15/2023 |
| 4199 | Cenetron Diagnostics Indianapolis, IN Associate Technologist Laboratory- 4 x 10s, Sat-Tues 8pm to 630am, rotating holidays Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 8/15/2023 |
| 4200 | Cenetron Diagnostics Milwaukee, WI Technologist Laboratory- Hemostasis Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1-3 years |
Under supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment. Supports the training of junior and peer staff members. Performs higher level interpretation of testing results and test panels. | 8/15/2023 |
| 4201 | Cenetron Diagnostics Wauwatosa, WI Research Technologist - Dr. Dipa Lab Bachelor's Degree from an accredited college or university in biology, chemistry, scientific discipline or equivalent combination of education and exp Exp: 1-3 years |
Under the direction of the Principal Investigator, performs laboratory assays and complex experiments to elucidate novel research questions. | 8/15/2023 |
| 4202 | Cenetron Diagnostics Wauwatosa, WI Research Technologist II - Flow Cytometry Core Lab Bachelor's Degree from an accredited college or university in biology, chemistry or equivalent scientific discipline required. Master's Degree preferr Exp: 1-3 years |
Under the direction of the Director, Core Laboratories develops, improves, and implements laboratory techniques and performs complex experiments or tests to contribute to the timely and accurate completion of research project(s) that involve flow cytometry. Works with Senior Coordinator Flow Cytometry Laboratory to provide the expertise and resources needed to contribute significantly to research projects that require fluorescence activated cell sorting and/or analysis. Stays current with information relative to the field of flow cytometry and the research being performed in the VBRI Flow Cytometry Core Lab. The successful candidate will have 1 or more years of flow cytometry experience and have demonstrated ability in flow cytometry techniques | 8/15/2023 |
| 4203 | Cenetron Diagnostics Indianapolis, IN Associate Technologist Laboratory- to Wed-Sat 8PM to 430AM w/ rotating holidays Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 8/15/2023 |
| 4204 | Cenetron Diagnostics Wauwatosa, WI Research Technologist - Histology Bachelor's Degree from an accredited college or university in biology, chemistry or equivalent scientific discipline required. Master's Degree preferr Exp: 1-3 years |
Position requires a bachelor’s degree or equivalent and demonstrated experience in research histology. Completion of an accredited histotechnology program is desired but not required. This position will report to the Director of VBRI Core Laboratories. | 8/15/2023 |
| 4205 | Champions Oncology Rockville, MD Research Technician I, Surgical Services BS degree in animal science, biology, pharmacology, or related field. Exp: 1 year |
Job Overview Support in vivo oncology research studies in mice as a member of the Surgical Services Team. Duties and Responsibilities: Perform survival surgical procedures on mice, including handling, restraint, tumor volume measurement with calipers or imaging device, anesthesia, surgical heterotopic tumor fragment and tumor cell implantations, euthanasia, tissue collection, and tissue cryopreservation. Record study data within the laboratory information management system. Read, understand, and adhere to study protocols. Perform general study preparation and organizational activities, including sample tube labeling, supply organization and stocking, and laboratory organization. Work weekends and holidays on rotating basis | 8/16/2023 |
| 4206 | Cisbio Annapolis, MD Research Technician II - Cell Culture Bachelor of Science degree. Exp: 6 months |
Responsibilities: Serves as subject matter expert for the Cell Services Research Technicians Assists Research Tech Supervisor in delegation of daily tasks and management of the Inventory Specialist team Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. | 8/16/2023 |
| 4207 | Cisbio Annapolis, MD CCFS Media Prep Technician Bachelor Degree in a chemistry, biology, or other relevant discipline. Exp: 0-1 year |
Responsibilities: Work with Cell Culture and Fermentation Suite scientists to prepare cell culture media, feed, stocks, buffers and reagents Primary duties will include preparing many types of biological cell culture basal media, nutrient feed and stock solutions for NS0, CHO and hybridoma cells Solutions will be tested for osmolarity, pH, and turbidity Using aseptic technique and a biological safety cabinet, filter or pump solution into sterile containers as requested by scientists and store all solutions properly Lab instrument maintenance for Nova, Cedex, BGA, pH meter and osmometer as schedule permits Monitor stock solution inventory and prepare as needed Label all solutions according to CCFS guidelines | 8/16/2023 |
| 4208 | Cisbio Annapolis, MD Research Technician - Cell Culture Bachelors Degree in science or chemistry. Exp: 6 months |
Responsibilities: Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. Perform established flow cytometry QC protocols on a routine basis and analyze results. | 8/16/2023 |
| 4209 | Cisbio Annapolis, MD Research Technician - Cell Culture Bachelors Degree in science or chemistry. Exp: 6 months |
Responsibilities: Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. Perform established flow cytometry QC protocols on a routine basis and analyze results. | 8/16/2023 |
| 4210 | Cisbio Annapolis, MD Research Technician - Cell Culture Bachelors Degree in science or chemistry. Exp: 6 months |
Responsibilities: Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. Perform established flow cytometry QC protocols on a routine basis and analyze results. Generate and analyze data with the highest Data Integrity standards to include identifying and reporting unusual results/outcomes. Operate and maintain laboratory instrumentation including Mycoplasma onsite testing & clean-up as warranted. | 8/16/2023 |
| 4211 | Cognate Bioservices Mattawan, MI Research Technician - Second Shift Operations *$1,000 sign on bonus *$20/hr starting wage 1 Bachelor’s/Master’s Exp: 0 years |
We are seeking a Research Technician for our Second Shift Operations at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives | 8/18/2023 |
| 4212 | Cognate Bioservices Mattawan, MI Research Analyst I- Formulations Bachelor’s/Master’s degree in a relevant field. Exp: 0 years |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. The pay range for this position is $23.50/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. The shift is for the weekend, Friday to Monday 6 AM-2:30 PM but will train for the first 12 weeks Monday-Friday 6 AM-2:30 PM. When you work Saturday or Sunday there will be a 10% shift differential. | 8/18/2023 |
| 4213 | Cognate Bioservices Durham, NC Research Technician I Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline. Exp: 1+ years |
We are seeking a Research Technician 1 for our Discovery site located Durham. The following are responsibilities related to the Research Technician 1: • Perform routine research activities as assigned, including in vivo-based screens. • Perform dosing of laboratory animals, animal husbandry. • Prepare & verify dosing solutions for administration. • Ensure that all individual study supplies are on-site & prepared in a timely manner. • Perform equipment maintenance. • Review protocol with manager to insure proper study execution. • Prepare & organize study data, study folders & data forms; perform data collection and entry. • Review study report, gives feedback on the accuracy of the materials & methods section; report data to more senior staff. The pay for this position is $24/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. | 8/18/2023 |
| 4214 | Cognate Bioservices Mattawan, MI Research Analyst I- Flow Cytometry Bachelor’s degree (BA/BS) Exp: 0 years |
We are seeking a Research Analyst I for our Flow Cytometry Team at our Safety Assessment site located in Mattawan, MI. Biomarkers (and Investigative Pathology) personnel are responsible for: The development, performance, and support of biomarkers and flow cytometry-based assays. Assisting in sample analysis for both the support of internal studies as well as external client-based studies in a GLP compliant environment. Including, but not limited to cytokine, hormone, renal, cardiovascular, osteo, complement, metabolic, and inflammatory markers. | 8/18/2023 |
| 4215 | Cognate Bioservices Mattawan, MI Research Analyst I - Immunochemistry Bachelor's degree (BA/BS) Exp: 0 years |
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 8/18/2023 |
| 4216 | Cognate Bioservices Mattawan, MI Research Analyst II, Discovery Bioanalytical 1 BS/BA in relevant field Exp: 1 year |
Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 8/18/2023 |
| 4217 | Companion Medical Memphis, TN R-D Engineer I Bachelors Mechanical Engineering or Technically degree required. Exp: 0 years |
As a R&D Engineer I, you will design and develop life-saving medical device products. Key responsibilities include leading new product development, conducting product testing and creating models and prototypes. You will actively seek out Voice of the Customer (VOC) input and translate that into product requirements, design specifications, and mechanical concepts. You will work under general direction and may serve as key functional core team member and/or leadership role in an extended team. The product focus will be on spinal implants and instrumentation to treat degenerative, deformity, and tumor/trauma conditions. | 8/18/2023 |
| 4218 | Companion Medical Memphis, TN R-D Engineer II Advanced degree Mechanical Engineering Exp: 0 years |
As a R&D Engineer II, you will design and develop life-saving medical device products. Key responsibilities include leading new product development, conducting product testing and creating models and prototypes. You will actively seek out Voice of the Customer (VOC) input and translate that into product requirements, design specifications, and mechanical concepts. You will work under general direction and may serve as key functional core team member and/or leadership role in an extended team. The product focus will be on spinal implants and instrumentation to treat degenerative, deformity, and tumor/trauma conditions. | 8/18/2023 |
| 4219 | Cook Biotech Bloomington, IN Manufacturing Engineer Bachelor’s Degree in Engineering. A degree in Mechanical, Electrical, Production, or Manufacturing Engineering preferred. Exp: 1+ years |
The Manufacturing Engineer 1 plans, directs, and coordinates manufacturing processes for medical device products, and supports Operations in a way to assure a quality product is produced in a timely manner. The Production Engineer works with Operations, Quality Assurance and Regulatory Affairs to improve existing product designs and processes to increase throughput, decrease operational costs, or improve quality. | 8/18/2023 |
| 4220 | Cook Biotech Vandergrift, PA Manufacturing Engineer 1 Bachelor’s Degree in Mechanical, Electrical, Production, or Manufacturing Engineering, or related field. Exp: 1+ years |
The Manufacturing Engineer primarily plans, directs, and coordinates manufacturing processes for medical device products, and supports Operations in a way to assure aquality product is produced in a timely manner, in addition to performing sustaining activities for commercially available products The Manufacturing Engineer works with Operations, Quality Assurance and Regulatory Affairs to improve existing product designs and processes to increase throughput, decrease operational costs, and improve quality while ensuring products and processes meet regulatory compliance. | 8/18/2023 |
| 4221 | Cooper Surgical Portland, OR Laboratory Technician 1 Bachelor's degree in Science. Exp: one to two years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 8/18/2023 |
| 4222 | Cooper Surgical New York, NY Laboratory Technician 1 - Evening Shift Bachelor's degree in a science field i.e. Biology, General Science, chemistry, etc. Exp: one to two years |
Performs routine semen banking procedures by performing the following duties. | 8/18/2023 |
| 4223 | Cooper Surgical New York, NY Laboratory Technician 1 - Evening Shift Bachelor's degree in a science field i.e. Biology, General Science, chemistry, etc. Exp: one to two years |
Performs routine semen banking procedures by performing the following duties. | 8/18/2023 |
| 4224 | Cooper Surgical New York, NY Laboratory Technician 1 - Evening Shift Bachelor's degree in a science field i.e. Biology, General Science, chemistry, etc. Exp: one to two years |
Performs routine semen banking procedures by performing the following duties. | 8/18/2023 |
| 4225 | Cooper Surgical Los Angeles, CA Laboratory Technician 1 - Evening Shift Bachelor's degree in Science. Exp: one to two years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 8/18/2023 |
| 4226 | Cooper Surgical Los Angeles, CA Laboratory Technician 1 - Evening Shift Bachelor's degree in Science. Exp: one to two years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 8/18/2023 |
| 4227 | Cooper Surgical Los Angeles, CA Laboratory Technician 1 - Evening Shift Bachelor's degree in Science. Exp: one to two years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 8/18/2023 |
| 4228 | CordenPharma Boulder, CO Chemical Process Engineer BS in Chemical Engineering Exp: 1 year |
Performs research and development activities for the purpose of transferring and designing/improving a process or technology. Provides process engineering support for manufacturing processes in assigned group or plant through developing and implementing continuous improvements. And through troubleshooting methods and equipment used in the production of bulk pharmaceutical intermediates and active pharmaceutical ingredients. | 8/18/2023 |
| 4229 | CordenPharma Boulder, CO QC Analyst - Nights Bachelor's Degree (BA) from 4-year college or university. Exp: 0+ years |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training Manual. Maintains a high level of housekeeping and attention to detail. | 8/18/2023 |
| 4230 | CryoLife Kennesaw, GA Process Engineer I (onsite) Bachelor’s degree in Engineering (Mechanical, Chemical, Biomedical, Industrial or related field of engineering). Exp: 0-2 years |
Responsible for providing process engineering support for all product manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as develop new processes to improve manufacturing efficiency. Supports new product launches by collaborating with other functional areas and providing process engineering expertise during the implementation of processes or equipment. | 8/18/2023 |
| 4231 | CryoLife Kennesaw, GA Lab Assurance Associate - Microbiology Record Review Bachelor’s Degree in the Life Sciences or an equivalent field of study preferred. Exp: 1+ years |
The Lab Assurance Associate will assist management in the review of Microbiology records to ensure they are compliant with required Standard Operating Procedures. Will ensure that all areas outlined under “Principal Responsibilities” are accomplished in an efficient, professional manner. | 8/18/2023 |
| 4232 | CSL Behring Waltham, MA Scientific Associate I (Protein Biochemistry) Bachelor or Master’s degree in Biochemistry or related biological sciences. Exp: BS: 1-3+ years; MS: 0-1+ years |
This position is responsible for the production and characterization of high quality purified recombinant protein of potential vaccine candidates. The ideal candidate would support development of cell cultures for expression of vaccine antigens and carries out protein purifications and characterizations. | 8/18/2023 |
| 4233 | Curi Bio Seattle, WA Laboratory Technician Bachelor’s degree in a scientific field is required. Exp: 1+ years |
Curi Bio is a rapidly growing startup company seeking a Laboratory Technician to join our team to perform cellular medium production, quality control and shipping/logistics. Prioritized candidates will have experience in aseptic cell culture, prior biotech experience, and experience with standard cell biology assays. Experience in quality control/assurance functions and/or logistics in a biotech atmosphere is highly desired. | 8/18/2023 |
| 4234 | Cyprotex Framingham, MA Research Associate BS/ MS in a relevant bio scientific discipline. Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays. | 8/18/2023 |
| 4235 | Cyprotex Rahway, NJ Research Associate B.S./M.S. in Molecular Biology, Synthetic Biology, Bioengineering, Biochemistry, or a related field. Exp: 1+ years |
There is an immediate opening for a motivated Research Associate to join the Reagents team in Evotec US. Evotec Reagents is a growing business unit delivering high quality materials to the pharmaceutical and agrochemical industry. Driven by business demand, our group was launched in Q1 2015 and is rapidly expanding, requiring suitable candidates to join this flagship operation. | 8/18/2023 |
| 4236 | Cyprotex Princeton, NJ Research Associate BS/BA in biology, biochemistry, engineering, or related scientific discipline Exp: 1-3 years |
The Assay Operations Group is seeking a talented and innovative Research Associate (full-time/permanent position) to join our growing team at Evotec’s US headquarters in Princeton, New Jersey. The successful candidate will join the Sample Management Group and provide assay automation support along with basic compound management support for the Assay Group. | 8/18/2023 |
| 4237 | Lonza Houston, TX Core Tech Viral Vector/Cell Therapy, BS or AA Life Sciences Exp: 0-1 year |
Responsible for aseptic processing of clinical grade product, participates in editing SOPs and batch records, maintains and stocks clean room environment with released inventory, monitors temperatures, expiration of materials and calibrated equipment; Supports cleanroom environment maintenance at below alert limits by following established cleaning practice; Packages kits, blood tubes and final product for shipment and monitors expiry of critical raw materials as needed; Complies with processes, procedures and instructions for all activities in which the team participates according to written guidelines and recognizes deviations from accepted practice; Responsible for carrying out production processes in a GMP facility, with tasks including cell culture | 08/15/23 |
| 4238 | Biodesix Boulder, CO Laboratory Technician II Bachelor’s degree in a chemical, physical, biological, or clinical laboratory science or medical technology • OR equivalent laboratory training and ex Exp: 1+ years |
Laboratory Technicians II assist with the setup and support of the daily activities of the laboratory. In addition, Laboratory Technicians II have the technical training and experience required to perform regulated clinical laboratory test realization (test specimen receipt through test result generation) using standard in-vitro laboratory techniques in Molecular Biology (PCR) and in Mass Spectrometry. Our focus areas of test development include oncology and virology. This experienced candidate is comfortable with SOPs and Work Instructions, working with data, standard laboratory chemicals, human blood specimens and is versed in standard molecular biology techniques (PCR, nucleic acid isolation/purification and sequencing). The position also works in a functional matrix organization, including Development, Customer Service, Accounting, Quality Operations management team, the Laboratory Directors, and other departments as needed. Ongoing training will be provided to supplement key skills required to perform the functions of this position as applicable. | 8/7/2023 |
| 4239 | Biodesix De Soto, KS Laboratory Technician I Bachelor’s degree in a chemical, physical, biological, or clinical laboratory science or medical technology; or equivalent laboratory training and exp Exp: 1+ years |
The Laboratory Technician I assists with the setup, support, and execution of the daily activities of the laboratory. In addition, a Laboratory Technician I will have the technical training and experience required to perform regulated clinical laboratory test realization (i.e., test specimen receipt through test result generation) using standard in-vitro laboratory techniques. Team members are also expected to operate a proprietary LIMS. The position also operates in a cross-functional matrix organization working across departments, including Development, Customer Service, Accounting, Quality, Operations, the Laboratory Directors, and other departments as needed. Ongoing training will be provided to supplement key skills required to perform the functions of this position as applicable. Required: must embrace a culture of transparency, willing and open to share data and technical knowledge, excellent communication skills, on time delivery of complete and quality results. Communicates issues promptly to manager with follow through to a resolution. Qualified Laboratory Technicians may act as responsible delegates according to the Biodesix Quality Matrix, including day to day responsibilities required for CAP/CLIA as well as all state-specific requirements in which Biodesix is an approved test facility. | 8/7/2023 |
| 4240 | Biogen Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred). Exp: Entry-Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 8/7/2023 |
| 4241 | Biogen Research Triangle Park, NC Manufacturing Associate II, Oral Solid Dose Bachelor’s Degree (STEM preferred). Exp: Entry-Level |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Oral Solid Dose area, and our teams operate across the following units: Dispensing, Blending, & Milling Compression Coating Encapsulation | 8/7/2023 |
| 4242 | Biogen Research Triangle Park, NC Manufacturing Associate III - Parenteral Filling Bachelor’s Degree (STEM preferred). Exp: 6 months |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling area, and our teams operate across the following units: Component Preparation Compounding Parenteral Filling/Lyophilization Visual Inspection | 8/7/2023 |
| 4243 | BioLegend San Diego, CA QC Development Research Associate Bachelor’s degree in a scientific discipline (preferably biology) Exp: 0 – 2 years |
At BioLegend, we are dedicated to commercializing high quality reagents to support the life science community for legendary discoveries that lead to cure. This position will contribute to improved QC assay development for current and new GMP bioprocessing products. The main GMP bioprocessing products are biologically active recombinant proteins, antibodies and cell culture media. The main responsibilities include performing studies and experiments to develop, optimize and validate the QC assay for launching new specifications for existing and new GMP bioprocessing products. In addition, He/She will assist with troubleshooting and contribute ideas to support product testing, assay improvement and on critical projects. The position also requires working closely with Product Development, Manufacturing, routine QC and QA teams to establish or modify assay SOPs. Additional responsibilities include generating and presenting data summaries, providing ETAs, and helping train others on experimental protocols and assisting with data review. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team. | 8/7/2023 |
| 4244 | BioLegend San Diego, CA Research Associate I - Cell Analysis Bachelor's in a Life Science related area. Exp: 1+ years |
The Research Associate I - Cell Analysis will be involved in product and reagent development for cell separation related applications. This position will have the opportunity to independently drive research projects from conception to completion, and will interact with multi-disciplinary teams. | 8/7/2023 |
| 4245 | Bioqual Rockville, MD Research Associate II BS/ MS in Life Science or similar field. Exp: 1+ years |
Ability to work with the Lab Supervisor to generate study related documents, and perform procedures including drug material formulation, challenge inoculum, treatments/therapeutics. Organized and detail oriented, especially would maintain detailed records on experimentation and reagent/ sample inventories. Good communication skills and a team player. Ability to multi-task with high level attention to details. Perform other duties as assigned. | 8/7/2023 |
| 4246 | Bioqual Rockville, MD Research Associate I BS in a related field Exp: 0-5 years |
The Research Associate I, under specific direction, performs a variety of basic and general laboratory research and clerical tasks determined by the field and scope of the particular research study. May perform tasks related to the research project independently, but within specific guidelines and subject to review by supervisor or other research staff. The Research Associate I is responsible for conducting in vitro experiments in order to produce reliable and precise data to support scientific investigations. The Research Associate I should be familiar with the SOPs relating to the laboratory for which they take responsibility for carrying out routine tasks accurately and following strict methodologies to perform a variety of analyses. They must have experience in laboratory techniques that are supportive of the intended research provided in approved protocol. | 8/7/2023 |
| 4247 | BioReliance Sheboygan Falls, WI Associate Production Scientist - 12 Hour Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, or other life science discipline. Exp: 0+ years |
*$7,000 Sign-On Bonus for 12 hour Night Shifts* Paid after 90 days of employment Your Role: As an Associate Production Scientist at MilliporeSigma, you will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department Perform operations to meet quality expectations throughout the process Perform routine assays, processes and/or unit operations Complete the volume of work required to achieve group/departmental goals and meet deadlines Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal) Communicate the status of operations and bring deviations to the attention of supervisor Provide complete and accurate records consistent with quality guidelines Ensure all applicable logbooks have been filled out completely as required by current procedures Interact with other departments as needed | 8/8/2023 |
| 4248 | BioReliance Rocklin, CA Production Lab Tech 1 Undergraduate Degree in Chemistry, Biochemistry, or other life science discipline Exp: 1+ years |
MilliporeSigma in Rocklin, CA is hiring a Production Lab Tech 1. The position is responsible for all tasks related to Production and Warehouse duties. This individual will work independently with a high level of attention to detail and in accordance with GMP regulations. | 8/8/2023 |
| 4249 | LGC Biosearch Technologies Petaluma, CA Quality Control Analyst I Bachelor’s degree in a relevant field such as Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or other directly related field. Exp: 1 years |
The Quality Control (QC) Analyst I focuses on the performance of analytical and functional testing activities within the QC chemistry lab. They are responsible for testing intermediate and finished chemical products, analysing the results of the QC testing and comparing results to established specification and customer requirements. In addition, they perform testing and/or review of incoming goods. This position reports to the Quality Control Supervisor or Quality Control Manger. This position requires a thorough understanding of basic laboratory etiquette, laboratory safety and chemical competency. This position will offer an in-depth understanding of the Quality Control process while additionally expanding knowledge of general analytical laboratory equipment such as the use of an HPLC, Spectrophotometer, and DNA synthesizers. | 8/8/2023 |
| 4250 | LGC Biosearch Technologies Petaluma, CA Oligonucleotide Production Technician I Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
The Oligonucleotide Production Technician I will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Synthesis department. | 8/8/2023 |
| 4251 | Bio-techne Minneapolis, MN Quality Control Technician Position requires an MLT/MLS degree, Bachelor’s degree in Biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. Other tasks include proofing labels and assay sheets. This position will adhere to safety regulations. Perform additional duties as assigned. | 8/8/2023 |
| 4252 | Bio-techne Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 8/8/2023 |
| 4253 | Bio-techne Minneapolis, MN Advanced Quality Assurance Specialist Master's degree in a biological or chemical scientific discipline. Exp: up to 2 years |
As an Advanced Quality Assurance (QA) Specialist you will support the quality functions of BioTechne through quality systems development and improvement, document and records review, auditing, and other quality functions. The Advanced QA Specialist will understand and follow appropriate quality procedures to meet compliance standards, including ISO 9001, ISO 13485, 21CFR11, and 21CFR820. This position will be responsible for supporting the Immunoassay Business Unit focusing on the Luminex product line. | 8/8/2023 |
| 4254 | Bio-techne Minneapolis, MN Research Associate, Antibody Applications B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
The Research Associate is responsible for routine quality control testing of antibodies using immunohistochemistry (IHC) and immunocytochemistery (ICC). The testing includes culturing and handling of stem cells, primary cells, and basic cell lines for the use in ICC. The handling of fixed tissues for use in IHC. The position requires routine documentation, data analysis and good communication of results. | 8/8/2023 |
| 4255 | Bio-techne Minneapolis, MN Research Associate, Analytical QC B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
As the Research Associate, Analytical Quality Control Analyst you will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include concentration determination, SDS-PAGE with densitometry, endotoxin assay, PCR, HABA, conductivity, total organic carbon and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis, and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned. | 8/8/2023 |
| 4256 | Bio-techne Wallingford, CT Quality Technician Bachelor of Science degree in relevant field. Exp: 0-2 years’ |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products. $22.00 to $25.00 per hour based on experience and qualifications | 8/8/2023 |
| 4257 | Bio-techne Austin, TX Advanced Research Associate Master’s degree in biology, molecular biology, biochemistry, genetics, or similar fields . Exp: 0-2 years |
Advanced Research Associates in our Research Group develop innovative nucleic acid technologies. This role will support new product initiatives by combining novel, highly multiplexed PCR technologies with analysis platforms such as qPCR, digital PCR, and long-read sequencing, and by integrating reagents, instrumentation, analysis algorithms, and software. Diagnostic disease applications span neurogenetics, (such as myotonic dystrophy, fragile X and autism spectrum disorder), oncology (liquid and solid tumors), carrier screening and other reproductive health applications. You will work in a cross-functional team to develop products and technologies that realize the next generation of molecular diagnostic tests. | 8/8/2023 |
| 4258 | bluebird bio Somerville, MA Associate Scientist II, Vector Process Development (Contract) MS in Bioengineering, Chemical engineering, Biology, Virology, Cell or Vector Biology or related biological sciences. Exp: 1+ years |
You’ll help to bring more patients their bluebird days by: Executing viral vector production experiments to assess the impact of process improvements and/or new technologies. All aspects of upstream and downstream viral vector production including mammalian cell culture, media preparation, culture initiation, seed train maintenance, transfection, filtration, and chromatography. Performing complex technical analytical work related to viral vector production, including cell-based assays, ELISA, flow cytometry and RT-PCR. Developing experimental plans, interpreting scientific results, providing statistical analysis where appropriate, summarizing and presenting scientific data and report progress on behalf of the team under the guidance of the senior scientists. Performing general laboratory tasks, including maintenance of equipment and inventory. Generating, managing, evaluating, and maintaining critical data in a highly organized manner including lab notebook maintenance with good documentation practices. | 8/9/2023 |
| 4259 | Camber Spine King of Prussia, PA Associate Project Engineer Bachelor’s degree in Mechanical Engineering (preferred), Biomedical Engineering, or other relevant technical discipline. Exp: 0-3 years |
The Associate Project Engineer will be involved with legacy and new product projects, including project planning, execution, while adhering closely to project timeline and budget | 8/10/2023 |
| 4260 | Cambrex Longmont, CO Associate Analytical Scientist II/III (QC) Associate Analytical Scientist II (QC): BS/MS in chemistry, biochemistry, or similar science-related field. Exp: 1+ years |
We are looking for a quality control chemist capable of testing all common analytical methodologies. This individual will have the ability to execute analytical methods as needed and is able to organize routine work with minimal instruction from management and accurately evaluate and interpret generated data. This individual will demonstrate an understanding of compliance as related to the analytical laboratory. | 8/10/2023 |
| 4261 | Cambrex Agawam, MA Analytical Analyst I Bachelor’s Degree (or advanced degree) in Chemistry or related science field required. Exp: 1+ years |
Analytical Analysts are responsible for a variety of daily Analytical laboratory operations to meet established testing requirements and turnaround time commitments to our medical device, pharmaceutical and biotechnology customers. | 8/10/2023 |
| 4262 | Advanced Sterilization Products Spring House, PA Associate Scientist I, CAR Screening Master’s degree in Life Sciences (e.g. Biology, Biotechnology) or a related field. Exp: 1-2 years |
The Cell Therapy team at Janssen Therapeutics Discovery is seeking a highly motivated lab-based Associate Scientist to join our Chimeric Antigen Receptor (CAR) Screening and Discovery team. The Associate Scientist I will join a cross-functional group of experts building a high throughput CAR screening pipeline for autologous and iPSC-derived effector cell types. The ideal candidate is an organized, self-driven scientist that thrives in a collaborative team-based environment, is excited to learn and has experience setting up in vitro functional assays to measure T cell function using both representative cell lines and primary human cells. Key activities will include performing in-vitro functional assays for large scale screening of CAR candidates, immune cell phenotyping through multi-color flow cytometry & cell line maintenance. Any experience in immunology, cell therapy and/or immuno-oncology is a plus but not required. | 8/10/2023 |
| 4263 | Advanced Sterilization Products Spring House, PA Associate Scientist, Downstream Process Development (Cell and Gene Therapy) Master’s Degree in Chemical Engineering, Biomedical Engineering, Biological Science, or related field. Exp: 1 year |
The candidate for this position will take the role of leading the downstream process development for the viral/ vaccine process scale-up and tech transfer within the Cell and Gene Therapy group in Spring House, PA. The primary responsibilities will include assisting in planning and designing of downstream experiments, leading the team towards successful execution of the planned experiments, optimize the process steps to improve or enhance the quality attributes of the molecule. | 8/10/2023 |
| 4264 | Advanced Sterilization Products Danvers, MA Product Development Engineer Cardiology BS in Mechanical, Biomedical Engineering or directly related scientific discipline. Exp: 1+ years |
The Cardiology Platform (Impella CP and Impella RP) is focused on rapidly developing the next-generation of percutaneously implanted Impella cardiac pumps. We are a dynamic development team that drives innovative solutions to improve patient care. As a Product Development Engineer you will support and own technical efforts, design initiatives, and engineering activities for next generation Impella systems. You’ll have a tangible impact on our business and be rewarded by a positive impact to patients' lives. | 8/10/2023 |
| 4265 | Advanced Sterilization Products Raynham, MA Quality Engineer Bachelor’s or equivalent University degree is required, recent graduates will still be considered. Exp: 1 year |
The Quality Engineer I should excel in an environment that embraces teamwork, change, risk-based decision-making, and flexibility. This individual will work in a design team setting. This individual will support design control activities for new product development. They will also support quality deliverables and tasks for commercialized devices on an as required basis. | 8/10/2023 |
| 4266 | Caris Life Sciences Phoenix, AZ Clinical Engineering Technician, Molecular Operations - Solid Tumor (3rd Shift) Bachelors or Master’s degree in a science field. Exp: one year |
The Clinical Engineering Technician is responsible for the organization, installation, and maintenance of the equipment within the clinical molecular lab. | 8/10/2023 |
| 4267 | Caris Life Sciences Phoenix, AZ Quality Assurance Technologist, Molecular - Liquid Profiling (2nd Shift) Bachelor’s degree in a science field. Exp: 1+ year |
A Quality Assurance Technologist is responsible for a multitude of different tasks within the clinical molecular laboratory including the quality control testing of all molecular reagents prior to use on clinical samples, assisting the product development team with the validation of new assays and training current employees on new assays as well as new employees on established assays. This position is required to be well versed in various molecular techniques that include, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, RFLP, DNA methylation analysis, Next Generation sequencing and automated liquid handlers. Quality Assurance Technologists are expected to contribute technically and intellectually to enhance efficiency within the lab while ensuring that the quality of reagents and training program is maintained to the highest standard. This position works under the direction of the Director and follows standard laboratory procedures and policies. | 8/10/2023 |
| 4268 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Liquid Profiling (3rd Shift) Bachelor’s degree in a science field is required. Exp: 1+ years |
The Molecular Technologist – Liquid Profiling is responsible for performing various molecular techniques that include, but are not limited to, blood processing and buffy coat extraction, RNA/DNA extractions, PCR, DNA methylation analysis, Next-Generation Sequencing, equipment maintenance, laboratory inventory, sample tracking and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 8/10/2023 |
| 4269 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Liquid Profiling (2nd Shift) Bachelor’s degree in a science field is required. Exp: 1+ years |
The Molecular Technologist – Liquid Profiling is responsible for performing various molecular techniques that include, but are not limited to, blood processing and buffy coat extraction, RNA/DNA extractions, PCR, DNA methylation analysis, Next-Generation Sequencing, equipment maintenance, laboratory inventory, sample tracking and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 8/10/2023 |
| 4270 | Caris Life Sciences Phoenix, AZ Molecular Technologist, Solid Tumor (2nd Shift) Bachelor’s degree in a science related field. Exp: Less than 1 year |
The Molecular Technologist I is responsible for performing various molecular techniques that include, but are not limited to, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, DNA methylation analysis, equipment maintenance, laboratory inventory, sample tracking, ordering supplies and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 8/10/2023 |
| 4271 | Caris Life Sciences Phoenix, AZ Reagent QC Specialist I - Molecular Bachelor’s degree in a scientific field is required. Exp: 1+ years’ |
The Reagent QC Specialist I – Molecular is responsible for maintaining compliance to all applicable regulatory requirements pertaining to the QC process for all incoming reagents which includes initial inspection upon receipt, performing applicable verification testing and assessment, and review of final QC paperwork before passing on to Process Quality for final reagent release into the laboratory. | 8/10/2023 |
| 4272 | Catalent Baltimore, MD Associate Scientist II, Cell Culture and Cell Line Development MS degree in a biological discipline (biochemistry, molecular biology, cell biology or equivalent). Exp: 1-3 years |
Reporting to a Senior Scientist for daily supervision, the Associate Scientist II – Cell-culture Innovation and Product development will work independently as well as collaboratively within our growing team in Biopark, MD. The individual should bring technical knowledge, initiative, strong scientific integrity, and an enthusiasm for learning to make measurable contributions within the group. | 8/10/2023 |
| 4273 | Catalent Greenville, NC Analytical Chemist I Bachelor’s degree a science-related discipline (e.g. Biology, Chemistry, Pharmaceutical Sciences). Exp: 0+ years |
Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. The Analytical Chemist I primarily performs routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. | 8/10/2023 |
| 4274 | Catalent Bloomington, IN Associate Scientist - QC Bachelor’s degree in science field OR Master’s degree in science field. Exp: BS: 0-3 years; MS: 0-2 years |
The Quality Control (QC) team is responsible for testing products, raw materials, and the manufacturing environment to ensure the safety, quality, identity, purity, and potency produced by the facility. The QC team is comprised of the following groups: microbiology, environmental monitoring, stability, release and in-process, method validation, sample management, raw materials, and other functions. This position requires a variety of skills necessary for biotech company operations. The position will perform routine testing of process samples, raw materials, finished products and stability samples, while adhering to SOPs and working in a cGMP compliant environment. The position will analyze and interpret results in written and oral format. Additionally, this position will support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system. Other duties will include data review/archiving, database entry/review, and contributions to process improvement initiatives. This is a permanent, full time position. It is a salaried role. The shift is Friday-Sunday 6:00am-6:30 pm. | 8/10/2023 |
| 4275 | Catalent Madison, WI Lab Associate, Upstream Process Development B.S/B.A. in Biotechnology, or related field. Exp: 1+ years |
The Upstream Process Development team is responsible for the development and implementation of upstream processing methodologies and analytical procedures that can be easily transferred to the cGMP Manufacturing Team. The Lab Associate, Upstream Process Development will perform a variety of laboratory procedures to support Upstream Process Development. The position will perform daily work assignments accurately and in a timely and safe manner. The Lab Associate, Upstream Process Development will perform routine scientific work, evaluating, selecting and applying standardized scientific procedures and techniques to assignments with clear, specific objectives; assignments require investigation of a limited number of variables and few complex features. Limited exercise of judgment is required on details of work and in making preliminary selections and adaptations of alternatives. This is a fulltime role working 8AM – 5PM Days; Monday – Friday | 8/10/2023 |
| 4276 | Catalent Madison, WI Assistant Scientist, Analytical Development B.S/B.A. in any STEM discipline. Exp: 0+ years |
The Analytical Development team is responsible for evaluating client analytical methods and/or optimizing/developing methods required to support cell line, upstream, and downstream development, and transferring them to the QC department for phase appropriate validation. The team is also responsible for characterizing primary and high order structures; confirming product comparability across scale and establishing product degradant profiles and specifications for reference standards of mRNA proteins/mAbs generated at Catalent’s, Madison site. The team executes on this by applying the concepts of analytical quality by design (AQbD) in compliance with FDA and other regulatory agency requirements and in conformance with the sites GMP quality systems. The team’s role is therefore central to the success of projects that enter cell line and process development and technology transfer workstreams and also ensures that analytical methods can be applied in establishing product critical quality attributes (CQA) and supporting IND-enabling studies and applications that are essential in providing high quality drug products for our clients and their patients. This is a full-time on-site hourly position, Monday - Friday 8:00am to 5:00pm CST. Please Note: This role may require some weekend shift work to support business need. | 8/10/2023 |
| 4277 | Catalent St Petersburg, FL Associate Scientist, QC BS or BA with college course work in related sciences. Exp: 1+ years |
The Associate Scientist II, QC will independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines. The Associate Scientist II, QC communicate results in written and oral presentations. Help in writing Procedures, Specifications and Test Methods. Keep abreast of literature in field; help train colleagues; contribute to continuous improvement within the group. Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. Maintain proper records in accordance with all SOP's and policies. | 8/11/2023 |
| 4278 | Norwich Pharmaceuticals Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline. Exp: 0-3 years |
The Quality Control Chemist I / Microbiologist I: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory | 8/2/2023 |
| 4279 | AnaSpec Fremont, CA Synthesis Chemist I BS or above in Chemistry, Organic Chemistry, or related disciplines. Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). As a member of the Synthesis department, the Synthesis Chemist I will work closely with the Purification, QC, and Sales & Business Development departments. | 8/2/2023 |
| 4280 | ANI Pharmaceuticals Baudette, MN QC Chemist/Sr. QC Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: QC Chemist – 1-3 years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 8/3/2023 |
| 4281 | Applied Medical Rancho Santa Margarita, CA Electrical Engineer I Bachelor’s degree in Electrical Engineering, Biomedical Engineering, Computer Engineering with an emphasis in Electrical Engineering or equivalent. Exp: 1+ years |
As an Engineer I (Sustaining/Manufacturing Electrical Engineer) you will be responsible for working within the framework of a team to provide engineering support to medical device development projects from design through production phase. You will be expected to design, investigate, develop, and qualify new manufacturing processes, fixtures, and equipment. Along with writing test protocols and reports, conducting various testing, collecting, and analyzing data and trends. | 8/4/2023 |
| 4282 | Applied Medical Rancho Santa Margarita, CA Biocompatibility & Sterilization Reporting Analyst Bachelor's Degree?in physical or biological sciences. Exp: 1+ years |
The Biocompatibility & Sterilization Reporting Analyst will support activities relating to the Biological Sciences team and its associated laboratories. Responsibilities will include coordinating all testing activities for bioburden, sterility, biocompatibility or other testing programs requiring outside services from a third-party laboratory. Testing will include both routine audits as well as R&D projects. You must be capable of writing protocols and final test reports and ensuring compliance with relevant standards, regulations, and guidance documents. | 8/4/2023 |
| 4283 | Applied Medical Rancho Santa Margarita, CA Quality Systems Engineer I/II – Test Method Validation Bachelor's Degree or higher in Engineering or a scientific field. Exp: one years' |
As an Engineer I/II on the Quality Systems (QS) Team, you will be responsible for working within the framework of a team and performing the following activities: Enhance product quality by developing and validating test methods that check for product performance and effectiveness Work closely with the Product and Process Development teams to understand user needs, design and process requirements and test method acceptance criteria Develop clear and testable methods using technical standards and engineering principles Design and create required test equipment | 8/4/2023 |
| 4284 | Applied Medical Rancho Santa Margarita, CA Process Engineer II/III Bachelor’s degree in Mechanical, Biomedical, Industrial, or Manufacturing Engineering (or equivalent). Exp: 1-4 years |
As a Process Engineer, you will work within the Group Process Development team and use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. The Process Engineer’s primary responsibilities are debugging, observing, and expediting shop orders. You will assist with developing and updating engineering documents and investigating new tooling, materials, manufacturing processes, and technologies. | 8/4/2023 |
| 4285 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I Bachelor’s degree in an Engineering or Science, Technology, Engineering, and Mathematics (STEM) field or related education and experience. Exp: 1+ years |
As a Quality Engineer I, you will learn and develop skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. | 8/4/2023 |
| 4286 | Applied Medical Rancho Santa Margarita, CA Plastics Process Engineer II Bachelor’s degree in Polymer, Materials, Plastics, or Manufacturing Engineering (or equivalent). Exp: 1-2 years |
As a Plastics Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. | 8/4/2023 |
| 4287 | Applied Medical Rancho Santa Margarita, CA Mechanical Engineer, Automation 4-year degree in Mechanical Engineering or in a related field. Exp: 1 year |
As a Design Engineer, you will play a vital role in supporting the development of automated machines or automated processes for our in-house medical device manufacturing. Below are some of the common skills and qualities that are sought after for this role. | 8/4/2023 |
| 4288 | Aquinnah Pharmaceuticals Cambridge, MA Research Associate Master’s degree in neuroscience, cell biology or related discipline. Exp: 1+ years |
The successful candidate should be highly motivated, flexible and enjoy working in a team - based environment with a strong interest in contributing to the discovery of new therapies for the treatment of neurodegenerative disease. This position is laboratory-based and requires strong experimental skills with a background in cell biology, molecular biology, or biochemistry. Under supervision, the candidate will assist in duties including, but not limited to: cell culture maintenance, compound screening, biochemical assays, immunocytochemistry, and analysis using state of the art high-content imaging. Strong communication skills are required including the ability to analyze and report on the results. The candidate will be expected to function efficiently and cooperatively within a team and maintain accurate and clear project records. The ideal candidate will be creative, energetic and motivated. Candidates should have a Bachelor’s or Master’s degree in neuroscience, biology, or related field. Salary will be competitive and commensurate with experience. | 8/4/2023 |
| 4289 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Responsibilities: Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 8/4/2023 |
| 4290 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline. Exp: six months’ |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. | 8/4/2023 |
| 4291 | Astute Medical Saint Louis, MO Associate Mechanical Engineer Bachelor's Degree in Mechanical Engineering or a related engineering discipline. Exp: 0 years’ |
This is a mechanical design engineering position with an emphasis on engineering design of complex medical instruments. This individual will collaborate with R&D engineering staff to design, document, prototype, and test complex medical instruments. | 8/4/2023 |
| 4292 | Astute Medical San Jose, CA V&V Microbiologist Bachelors Degree in microbiology or related science discipline. Exp: one year |
Specific is seeking a Verification and Validation (V&V) Microbiologist with experience in Research and Development. You will be a key contributor and critical to the success of the company. As part of the V&V team, you will be responsible for testing, documenting, and evaluating instruments and consumables to support the company’s product lines. You will be responsible for writing specifications, testing protocols, and processes that ensure that test materials/products are reliable and repeatable. As part of the Microbiology team, you will help build up toward commercial readiness of our products and will execute laboratory functions as listed below. | 8/4/2023 |
| 4293 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 8/4/2023 |
| 4294 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 8/4/2023 |
| 4295 | Astute Medical Salt Lake City, UT Research Associate I Bachelor's degree in a scientific discipline. Exp: six months’ |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and bioMérieux. A Research Associate I may receive general or detailed instruction and direct supervision on general work, new procedures, and assignments. | 8/4/2023 |
| 4296 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline. Exp: entry-level |
This is a full time non-exempt position. This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. Performs general lab duties, designs and conducts experiments, collects and analysis data and keeps an accurate record of all work done in accordance with the quality system. Requires some problem solving skills. Normally receives general instructions on routine work, detailed instruction on new assignments. Reports to the System Validation Manager. | 8/4/2023 |
| 4297 | Atalanta Therapeutics Boston, MA Associate Scientist I/II, In Vitro Biology Master’s degree in biochemistry or relevant biological science. Exp: 0-2 years |
Atalanta is seeking a highly motivated individual to join our In Vitro Biology team to contribute to the preclinical development of RNAi-based therapeutics. The selected individual will design and execute biochemical assays for the quantification of therapeutic oligonucleotides and contribute towards their profiling of pharmacokinetic properties. The Associate Scientist will be responsible for supporting multiple drug development programs for neurodegenerative diseases. This is an ideal position for candidates who thrive in a team-oriented, fast-paced, and cross-disciplinary environment. | 8/4/2023 |
| 4298 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, siRNA Screening Master’s degree in biochemistry or relevant biological science. Exp: 0-2 plus years |
Atalanta Therapeutics is seeking an experienced and highly motivated Associate Scientist II or Senior Associate Scientist to be part of the dynamic and collaborative In Vitro Biology team. This individual will contribute to cell-based screening of therapeutic oligonucleotides under direction of the HTS lab head. The Associate Scientist II/Senior Associate Scientist will be responsible for routine cell line maintenance, optimization of medium to high-throughput cellular assays to quantitate mRNA or protein marker levels, and execution of siRNA efficacy screens to support preclinical drug development for multiple therapeutic targets. The ideal candidate will be flexible to changing priorities/timelines and have strong attention to detail, organization and communication skills. | 8/4/2023 |
| 4299 | ATUM Newark, CA Gene Synthesis Production Associate Bachelor’s degree in Biology Exp: entry-level |
ATUM is looking for a new member for our Gene Synthesis Production Group. ATUM is a leading bioengineering solutions provider, offering an integrated pipeline of solutions including gene design, gene synthesis, expression vectors, protein expression, protein engineering, cell line development, and master cell banking. Our products and services support breakthroughs across the life sciences. ATUM delivers DNA, proteins and cells that transform biology from a discovery science to an engineering discipline, improving the way people research, create, and live. This entry-level position is within our Gene Synthesis production group. The work includes following standard operating procedures, using automated liquid handling equipment, interfacing with our in-house database, providing support in various lab functions, and interacting with our bioinformatics department. | 8/4/2023 |
| 4300 | August Bioservices Nashville, TN Formulation & Component Prep 2nd Shift BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician II – Component Preparation and Formulation will operate a variety of processing and packaging equipment to prepare components for aseptic filling to include bulk formulation of aqueous and non-aqueous based products, order and receive components, dispense and formulate raw materials, manage sterilized components, operate various equipment used in the formulation process, and perform cleaning operations for process equipment and the GMP ISO 8 areas. | 8/4/2023 |
| 4301 | August Bioservices Nashville, TN Manufacturing Technician II – Filling, Lyophilization, & Terminal Sterilization 2nd Shift BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year or more |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician II – Filling, Lyophilization, and Terminal Sterilization will use proper aseptic technique while performing tasks in aseptic manufacturing areas to include syringe and vial filling operations with an automated line in an RABS environment as well as routine and non-routine aseptic interventions through RABS glove ports. The technician II level will operate filling and auto loading equipment, and freeze dryers using automated control systems. The Technician II will be responsible for unloading of autoclaves, performing cleaning operations for process equipment and the GMP ISO 8 areas, management of sterilized components, and coordinating with maintenance as needed | 8/4/2023 |
| 4302 | August Bioservices Nashville, TN Microbiologist I B.A./ B.S in Biology (or related) Exp: 0–2 years |
August Bioservices is looking for a Quality Control team member that is passionate and driven professionally. August Bioservices desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. Reporting to the Manager, Microbiology, the Microbiologist I will be responsible for performing biological assays of raw materials, in-process samples, finished product, and environmental monitoring samples. He/she will work with microbiology personnel to assure test results, procedures, and methods are written, maintained, executed, and approved in accordance with approved SOPs and regulatory requirements. | 8/4/2023 |
| 4303 | Avalign Technologies Fort Wayne, IN Product Engineer Bachelor's Degree or equivalent experience required. Exp: 1+ years |
We are searching for a Product Engineer to join our team that will be responsible for the following: develop, establish and maintains engineering methods and systems to meet site specific, customer and regulatory requirements. Actively communicate initiatives to support departmental, plant and corporate operational goals. Serve as an engineering representative to provide support and guidance for new product transfers through volume production internally, at suppliers, and at customer locations. Drive new product introductions to meet customer specifications and delivery expectations. | 8/4/2023 |
| 4304 | Avantor Sciences Carpinteria, CA Process Engineer I Process Engineer I bachelor’s degree in chemical engineering Exp: 1-2 years |
Avantor is seeking an R&D Process Engineer who will be responsible for new product development of fabricated parts, process improvement projects, and capital projects ensuring the successful conclusion of all phases within an appropriate time and at appropriate cost. This role will be a full-time position based out of our Carpinteria, CA office. You will have the opportunity to implement process improvements to meet quality standards, perform feasibility studies, and solve problems. This position is involved in implementing step-change process improvements. | 8/4/2023 |
| 4305 | Avantor Sciences Bakersfield, CA R&D Chemist R&D Chemist Bachelor's degree in chemistry or biochemistry required. Exp: 1 to 3 years |
Avantor is seeking an Entry-mid level R&D Chemist to research product formulations and properties of raw materials. This person will also prepare and provide samples for laboratory and field testing for efficacy and safety and establish product specifications and procedures for R & D projects. This role will be a full-time position based out of our Bakersfield, CA office. You will have the opportunity to develop reports and documents detailing project processes, results and conclusions, and conduct research and field evaluations on new products! | 8/4/2023 |
| 4306 | Avantor Sciences Bakersfield, CA Quality Control Technician - Testing (3rd Shift) Quality Control Technician - Testing (3rd Shift) BA/BS in chemistry or science-related field preferred. Exp: 1-2 years |
Avantor is looking for a dedicated and experienced Quality Control Technician 3rd Shift. Working in partnership with under close supervision, responsible for completing product quality checks. Conducts routine testing and analysis of production work. Quality checks are typically reviewed for accuracy. Documents quality control issues as needed. This role will be a full-time position base out of Bakersfield, CA. 3rd Shift 10:00PM – 6:30AM | 8/4/2023 |
| 4307 | Avantor Sciences Irving, TX QC Lab Analyst QC Lab Analyst Bachelors of Science in Chemistry or related field. Exp: 1-2 years |
Avantor is looking for a dedicated and proactive QC Lab Analyst to optimize our NuSil team, delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of our Irving, TX facility. You will have the opportunity to inspect and process raw materials before releasing finished products. If you have experience in quality control and are eager to grow your career - let's talk! | 8/4/2023 |
| 4308 | Avantor Sciences Saint Louis, MO Quality Control Laboratory Technician Quality Control Laboratory Technician Bachelor’s degree in a science discipline such as Chemistry, Biology, Microbiology Exp: 1+ years |
Avantor, a Global Fortune 500 company, is looking for a dedicated Quality Control Laboratory Technician to optimize our Quality Control organization. This on-site/ Saint Louis, MO role is full-time. If you have laboratory experience – let’s talk! | 8/4/2023 |
| 4309 | Aviva Systems Biology San Diego, CA Research Associate I/II – Molecular Biology B.S. or M.S. in life science or related subject. Exp: 1+ year |
Job Responsibilities Perform routine biochemistry and molecular biology techniques such as cloning, RNA/DNA isolation, cell culture, and protein purification Perform small-scale bacterial, fungal, and mammalian cell culture using aseptic techniques Operate incubator/shakers, centrifuges, and other laboratory equipment used in protein production Use electrophoresis and chromatography systems for biomolecule analysis or purification Prepare chemical solutions required for production processes Analyze Sanger sequence data for validation of expression constructs | 8/4/2023 |
| 4310 | Avomeen Ann Arbor, MI Chemist II Masters in Chemistry or Pharmacy Exp: 0-3 years |
Element has an opportunity for a Chemist II to join our growing team in Ann Arbor, MI. The Chemist II supports development of analytical methods, perform testing using a variety of technologies and draw conclusions based upon analytical data. Supports validation studies or complex sample analysis with guidance of senior staff members. Gains exposure to some of the complex tasks within the job function with moderate supervision. | 8/4/2023 |
| 4311 | AxoGen Dayton, OH Quality Analyst - 2nd Shift Bachelor’s Degree in an Engineering, Life Science discipline and/or in a related field. Exp: 0-2 years |
Axogen is hiring for a 2nd shift Quality Analyst in Dayton, OH! Job Summary of the Quality Analyst The Quality Analyst is responsible for providing quality on the floor oversight to first, second, or third shift. In this role, they will be responsible for printing batch record and other forms as needed, providing quality oversight and training to operators, performing on the floor review, performing quality control (QC) inspection and disposition of materials and products according to specifications, and performing final batch record review and product release activities. | 8/4/2023 |
| 4312 | Bausch & Lomb Rochester, NY Chemist I BS in Chemistry, or related field. Exp: 1-3 years |
The Scientist I - Chemistry is a member of a lab-based team in the Quality organization responsible for monitoring product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 8/4/2023 |
| 4313 | BGI San Jose, CA LC/MS Research Associate – Small Molecule B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
San Jose Mass Spec Lab of BGI Americas is seeking an exceptional and motivated research associate with competitive compensation. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up metabolomics and lipidomics capability in SJMS lab, 4) to support other departments when needed. A candidate with metabolomics/lipidomics LC-MS experience is a plus; a candidate with small molecule sample prep experience is a plus. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for metabolomic or lipidomics analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and working with biofluids is a plus. | 8/4/2023 |
| 4314 | BGI San Jose, CA LC/MS Research Associate – Proteomics B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
BGI Americas San Jose Mass Spec (SJMS) center is seeking an exceptional and motivated research associate to join our Proteomics department at our San Jose facility. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up additional proteomics capability in SJMS lab, 4) to support other departments when needed. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for proteomics and biologics characterization analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and, working with biofluids is a plus. | 8/4/2023 |
| 4315 | Bioagilytix Durham, NC Analyst - ADA/PK - 1 Bachelor's degree in molecular biology, biochemistry, immunology, biotechnology, or related field. Exp: one (1) year |
Essential Responsibilities: Run assays independently Adhere to provided method/directive Prepare buffers Use LIMS system Participate in sample analysis Pipetting Adhere to safety requirements Keep accurate inventory of supplies for assays Responsible for accurate record keeping with regard to sponsor's samples, data, and reports (documentation according to GxP guidelines) | 8/4/2023 |
| 4316 | Bioagilytix Durham, NC Analyst - ADA/PK - 3 (JC) Bachelor's degree in molecular biology, biochemistry, immunology, biotechnology, or related field. Exp: one (1) year |
Essential Responsibilities: Run assays independently Adhere to provided method/directive Prepare buffers Use LIMS system Participate in sample analysis Pipetting Adhere to safety requirements Keep accurate inventory of supplies for assays Responsible for accurate record keeping with regard to sponsor's samples, data, and reports (documentation according to GxP guidelines) | 8/4/2023 |
| 4317 | Bioagilytix Boston, MA Analyst - ADA/PK -1 Bachelor's degree in molecular biology, biochemistry, immunology, biotechnology, or related field. Exp: one (1) year |
In this role, you will perform validation studies through the analysis of biological samples. Our clients trust us to deliver excellence in data and bioanalysis, and this role is a bedrock within our project lifecycle. You will work on a wide variety of sample validations, including biologics, protein, peptides, small molecules, and/or biomarkers with a team of expert scientists. This role is also exposed to a range of analytical instrumentation and each project looks different than the previous one. At BioAgilytix, we don’t limit you to only extracting samples - we train you to become a scientist. We are looking for candidates who have scientific lab experience in a deadline-driven setting. The best candidates are people who have hands-on experience in a lab environment (academic or professional) and are curious about applying different scientific methods, equipment and extraction processes. If you are a person who is energized by project variety and learning from top scientists in our industry, then you’ll be right at home here at BioAgilytix. | 8/4/2023 |
| 4318 | AbbVie South San Francisco, CA Associate Scientist, Conjugation Chemistry B.S. degree or M.S. degree with experience in Analytical chemistry, Biochemistry, Chemistry or other relevant discipline. Exp: 0-3+ years |
AbbVie has an opening for an Associate Scientist in Discovery Research to conduct pre-clinical research and development in the area of antibody drug conjugates (ADCs). Key Responsibilities Include: Synthesis, purification and characterization of ADCs on mg to gram scale under minimal supervision. Optimization and validation of conjugation protocols and formulation buffers. Optimization of automated techniques for ADC synthesis and purification. | 7/25/2023 |
| 4319 | AbbVie Irvine, CA Associate Scientist II/Scientist I, in vivo MS or equivalent education in pharmacology, immunology, neurobiology. Exp: 0-2+ years |
The AbbVie Ocular Discovery Research group is seeking an experienced in vivo scientist to make substantial contributions to glaucoma disease research and discovery efforts developing therapies for optic neuropathy. S/he/they will execute, develop, and communicate in vivo experiments for target identification/validation and discovery of novel therapeutics using a variety of ocular disease based in vivo rodent models. The successful candidate will leverage in vivo rodent model experience to find answers to scientific questions and move projects forward. They should be a highly motivated, hands-on scientist who is also capable of executing on scientific projects. Emphasis is on the ability to successfully perform hands-on work, demonstrate scientific skills and communicate results. Prior experience in the fields of neuroscience, ophthalmology, retinal degeneration, or vision research is preferred, but not required. In addition, the candidate should be able to manage multiple projects simultaneously and work successfully in a cross-functional and highly collaborative team environment. | 7/25/2023 |
| 4320 | AbbVie Cincinnati, OH Technician, Manufacturing II Bachelor's Degree in Engineering Exp: 0+ year |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/25/2023 |
| 4321 | AbbVie Worcester, MA Manufacturing Technician, Wed - Sat, 1st shift BS in science Exp: 1+ years |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/26/2023 |
| 4322 | AbbVie Worcester, MA Manufacturing Technician, Wed - Sat, 2nd shift Bachelor's Degree in Engineering Exp: 0+ year |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/26/2023 |
| 4323 | AbbVie Worcester, MA Manufacturing Technician, Sun - Wed, 2nd shift Bachelor's Degree in Engineering Exp: 0+ year |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/26/2023 |
| 4324 | AbbVie Worcester, MA Manufacturing Technician, Wed - Sat, 2nd shift Bachelor's Degree in Engineering Exp: 0+ year |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/26/2023 |
| 4325 | ABEC Bethlehem, PA Product Engineer - Process Sciences Bachelor's degree in Engineering, Life Sciences, or Sciences field (Biological, Chemical, Physics, or equivalent experience). Exp: 1 year |
The Process Sciences Engineer is responsible for collaborating, leading, and executing process sciences efforts, specifically focused on Computational Fluid Dynamics Modeling and Empirical Data Generation to support internal or/and external projects during the implementation new technology; knowledge generation or any ABEC key activity. This role involves create predictive models, conducting experiments, collecting, and analyzing data, protocol and report preparation, and customer interaction. For this role, a certain level of independency and initiative is needed. Additionally, the Process Sciences Engineer will contribute to activities such as marketing content generation, new product development support, and sales and services. | 7/26/2023 |
| 4326 | Analytical Biological Services Wilmington, DE QC Laboratory Associate BS or BA or higher in biological sciences or equivalent field. Exp: 1+ years |
The QC laboratory associate is responsible for performing quality control testing with rapid turnaround and accurate results, to ensure high quality of our cell culture products for our clients. The associate must understand the basics of molecular biology, cellular biology, and cell culture and will be responsible for job management following the completion of the production phase through the transition to shipment or storage. Successful job management will include performing tests in-house, preparing samples for outsourcing, accurate record keeping, and communication of results, knowledge, and product information to team members and clients. This position requires strong time management, attention to detail, organization, precise record keeping, and excellent communication skills. | 7/26/2023 |
| 4327 | Analytical Biological Services Wilmington, DE Cell Culture Scientist BS or BA or higher degree in biological sciences. Exp: 1+ years |
Cell Culture Scientist position is currently available in Wilmington, DE. ABS Inc. (www.absbio.com) is a successful bioscience company with over 29 years’ experience providing cell culture and other services for R&D to pharmaceutical and biotechnology clients worldwide. | 7/26/2023 |
| 4328 | Analytical Biological Services Wilmington, DE Biorepository Technologist I (In-Sourced) Bachelor’s Degree in a medical or biological science preferred. Exp: 1+ years |
Primary duties and responsibilities of the Biorepository Technologist I (In-Sourced) included but are not limited to: -Receive biospecimens including frozen, fixed, or fresh solid and liquid samples -Coordinate with shipping and receiving department to ensure all shipments are appropriately tracked -Coordinate with internal clinical study team to ensure sample and data accuracy -Communicates by written and verbal methods with related departments to assure samples arrive in the appropriate lab -Record sample quality concerns and provide feedback to collection site or central lab -Document sample information in laboratory database from source documents -Accession samples and appropriate data in the laboratories electronic data management system -Pull samples from inventory when requested by scientists for internal projects | 7/26/2023 |
| 4329 | Abveris Boston, MA Research Associate - Protein Analytics Bachelor’s or Master’s degree in a scientific discipline required (Biology, Biochemistry, Biochemical Engineering) Exp: 1-3 years |
We are seeking a motivated individual to join our team and expand our bioanalytical department. Using state-of-the art technologies and workflows, this Research Associate would work with the Protein Analytics team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 7/26/2024 |
| 4330 | Abveris Boston, MA Research Associate - Molecular Biology Degree in Biology or other related discipline Exp: 1+ years |
We are seeking a motivated individual to join our Molecular Biology team and contribute to cloning, antibody sequencing, single B cell discovery and additional molecular biology workflows. The role will be lab-based and integral to expanding our molecular biology capabilities as our company continues its rapid growth trajectory and passion for integrating state-of-the-art technology and custom antibody discovery techniques. The ideal candidate will have previous hands-on experience with immune cell sample processing, PCR amplification and cloning techniques. Technical proficiency in a combination of the following is also desired: Next Generation Sequencing (NGS) workflows, antibody sequence analysis and high throughput downstream molecular biology techniques required for various cloning methods and subsequent recombinant expression. Meticulous attention to detail, proficient reasoning and problem-solving skills are cornerstones for a successful candidate. | 7/26/2023 |
| 4331 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst I B.S. degree in a relevant scientific discipline Exp: 0-2+ years |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 7/26/2023 |
| 4332 | Acumed Addison, TX Quality Engineer 1 Bachelor’s degree in an engineering or science discipline. Exp: 0-3 years |
The Quality Engineer 1 is responsible for supporting all quality activities related to the production and inspection of sustaining products. The QE 1 drives Quality objectives in all sustaining activities, ensuring product and process conformance to global standards (including FDA AND ISO 13485). The purpose of this position is to serve as a Quality leader during manufacturing to ensure high product quality, reliability, and process capability and facilitate teams in identifying, documenting, assessing, correcting, and presenting quality issues using risk analysis and root cause analysis tools. | 7/26/2023 |
| 4333 | ADMA Biologics Boca Raton, FL Raw Material Specialist I B.S. or associate degree in Chemistry, Biochemistry, Biology or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Raw Material Specialist I! The Raw Material Specialist I will perform quality control raw material processing and testing. Following general instructions on routine work and detailed instructions on new assignments. | 7/26/2023 |
| 4334 | ADMA Biologics Boca Raton, FL Technician I Fill Finish Operations - Night Shift Bachelor’s degree or equivalent experience Exp: Entry-Level |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Technician I Fill Finish Operations - Night Shift in Boca Raton, FL! The Technician I Fill Finish Operations - Night Shift position is responsible for the final finishing of plasma products. This includes aseptic filling, visual inspection, vial labeling, and final serialization and packaging. This position is under oversight of the Group Leader and reports to the Supervisor/ Sr. Manager Fill Finish Operations. | 7/28/2023 |
| 4335 | ADMA Biologics Boca Raton, FL Technician I Fill Finish Operations - Day Shift Bachelor’s degree or equivalent experience Exp: Entry-Level |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Technician I Fill Finish Operations - Day Shift in Boca Raton, FL! The Technician I Fill Finish Operations - Day Shift position is responsible for the final finishing of plasma products. This includes aseptic filling, visual inspection, vial labeling, and final serialization and packaging. This position is under oversight of the Group Leader and reports to the Supervisor/ Sr. Manager Fill Finish Operations. | 7/28/2023 |
| 4336 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences. Exp: BS: 1-3 years; MS: 1 year |
Admera Health is looking for an Associate Scientist I/II to join our growing team! | 7/28/2023 |
| 4337 | Akoya Biosciences Marlborough, MA Research Associate II (Tuesday through Saturday shift) AS or BS Degree in Life Sciences. Exp: One (1) to five (5) years |
Please note: The position is a full-time, on-site role working in the Akoya Advanced Biopharma Solutions (ABS) laboratory located at Marlborough, MA and the work schedule is Tuesday through Saturday. Position Summary/Impact: We are seeking for a highly motivated Research Associate II to join the Akoya Advanced Biopharma Solutions (ABS) group located in Marlborough, MA. The successful candidate will work in a team-oriented environment providing clients with multiplexing immunofluorescence staining. The candidate will have worked in a clinical or preclinical pathology laboratory with experience in high-throughput histology with focus on immunohistochemistry. The candidate will work with lab personnel on reagent preparation, troubleshooting and running qualification studies. Knowledge of antibody validation methods, immunofluorescence (IF) and quantitative pathology approaches are a plus but not required. The successful candidate must have experience in basic image analysis and be part of a team that provides imaging for clients. They should also be familiar with LIMS systems and have experience working in a regulated laboratory setting such as a CAP/CLIA and GCLP. | 7/28/2023 |
| 4338 | Alcami Wilmington, NC Associate Scientist I/II Bachelor’s degree in Chemistry or related field. Exp: 0 – 4+ years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. This position may also be required to work on method development/method validation projects. Typical types of testing include: assays (potencies, related substances, residual solvents, metals etc.), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, DSC, TGA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client/vendor supplied or developed by Alcami). The Associate Scientist II must have the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data is required. The Associate Scientist II will occasionally be called upon to support and mentor other Analytical Chemists within the lab. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/28/2023 |
| 4339 | Alcami Wilmington, NC Associate Scientist I/II -Microbiology Bachelor’s degree in Chemistry, Biology, Microbiology or a related field with course work in Microbiology. Exp: 0 – 4 + years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing microbiological routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing and stability. Bacterial endotoxins, sterility, microbial examination and antimicrobial effectiveness based methodologies are commonly employed in the described testing. Other key methodologies applied include: liquid particulate matter and genetic identification testing. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client/vendor supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/28/2023 |
| 4340 | Alcami Charleston, SC Associate Scientist I/II Microbiology 2nd Shift Bachelor’s degree in Chemistry, Biology, Microbiology or a related field with course work in Microbiology. Exp: Level I: 0 – 2 + years |
The Associate Scientist is accountable for driving results in a fast-paced environment. Level I is responsible for performing and documenting the monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The incumbent will provide support to manufacturing and laboratory operations. Level II is responsible for performing complex microbial analysis and assisting with method development and validation. The position plays an important role in environmental monitoring through accurate sampling and leadership of junior employees. The Associate Scientist II may assist in GMP review, provide problem solving support and Laboratory Investigation Report ownership for the Microbiology Department. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/28/2023 |
| 4341 | Alcami Morrisville, NC Associate Scientist II - Raw Materials Bachelor's degree in Pharmaceutical Sciences or Chemistry or Master's degree. Exp: BS: 1 years; MS: 0 years |
The position is responsible for support of compendial testing group and manages priorities of this team to provide the timely, compliant and accurate testing of raw materials, critical utilities, in-process samples and finished product. This position will collaborate with cross-functional teams and will work side-by-side with other scientists and professionals to drive the scientific agenda. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/28/2023 |
| 4342 | Aldevron SE Bothell, WA Oligonucleotide Manufacturing Chemist BS in Chemistry, Biochemistry preferred. Exp: 0-2 years |
The Oligonucleotide Manufacturing Chemist supports manufacturing of synthetic oligonucleotides under a cGMP environment for use in Cepheid in-vitro diagnostic products. The Chemist will use scientific knowledge and understanding to execute and document standard operating procedures to ensure successful manufacturing and on time delivery of Oligonucleotides. They will contribute to the successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization and support processes to ensure performance within expected parameters. This position is part of the Oligonucleotide Manufacturing team and will be located onsite in Bothell, Washington facilities. | 7/28/2023 |
| 4343 | Aldevron SE Bothell, WA Manufacturing Chemist Master’s degree in Chemistry, Biochemistry, Chemical Engineering or a related field. Exp: 0+ years |
The Manufacturing Chemist is responsible for performing tasks associated with the production of oligonucleotides in a dynamic fast paced GMP manufacturing environment. The position will also work closely with development and Quality teams to transfer and qualify new technology and processes from development into manufacturing. This position is part of the Oligonucleotide Manufacturing team and will be located onsite in Bothell, Washington facilities. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 7/28/2023 |
| 4344 | Aldevron Miami, FL Manufacturing/Process Engineer II Master’s degree. Engineering degrees in mechanical, electrical, and industrial preferred. Exp: 0+ years |
The Manufacturing/Process Engineer II for Beckman Coulter Diagnostics is responsible for providing day to day technical support and driving complex root cause investigations, for the instrument manufacturing product lines, including the assembly and final test processes, to drive quality and on-time delivery for our customers. This position is part of the Manufacturing Operation located in Miami, Florida and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Engineering Team and report to the Manufacturing Engineering Manager responsible for providing technical support to the manufacturing lines of Beckman Coulter’s premier Diagnostics products. | 7/28/2023 |
| 4345 | Aldevron Madison, WI Associate Scientist II, Upstream Biomanufacturing (Fermentation) B.S. degree Exp: 0-2 or more years’ |
The Associate Scientist II position is part of the Upstream Biomanufacturing department located in Madison, WI and will be onsite. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Upstream Biomanufacturing team and report to the Manager of Upstream Biomanufacturing and will be responsible for supporting the execution of 1-L to 1000-L scale microbial fermentations. This role works collaboratively with team members and as an individual contributor. This position requires excellent laboratory skills, attention to detail and excellent documentation practices. | 7/28/2023 |
| 4346 | Aldevron Boston, MA Lab Scientist, Spatial Biology BS is the minimum educational requirement (preferably in the biological sciences). MS in biological sciences is strongly preferred. Exp: 1+ years |
Come join the spatial biology team at Leica Microsystems. We are a rapidly growing group in an exciting scientific space, and we come to work every day knowing we can make a difference in human health. In your role as Lab Scientist, you will carry out projects based on multiplexed imaging, including tissue/cell prep, imaging and analysis. Be prepared to use your creativity and problem solving skills to help the team develop new solutions. Ensures laboratory environment and practices comply with guidelines set forth by company and regulatory agencies This role is hybrid and based out of our new Waltham, Massachusetts location . | 7/28/2023 |
| 4347 | Aldevron Madison, WI Associate Scientist II - Upstream PD Bachelor’s degree in biology, biotechnology, molecular biology, biochemistry, chemistry, or a closely related field. Exp: 0-2 years |
This position is part of the Upstream Process Development Team located in Madison and will be on-site. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Upstream Process Development Team and report to the Manager responsible for assisting on protein expression projects and media preparation. | 7/28/2023 |
| 4348 | Alliance Pharma Malvern, PA Assistant Scientist I BA/BS or higher; all experiences will be evaluated. Exp: 1+ years |
Responsibilities: · Prepare reagents, standards, and control samples · Analyze samples using various techniques specific to department · Operate analytical equipment · Maintain analytical equipment · Ensure lab area is clean and inspection ready at all times · Remove lab waste · Record tasks in accordance with Good Documentation Practices (GDP) · Learn and apply regulatory requirements; GLP, GCP, 21CFR Part 11 · Follow applicable SOPs and procedural documents · Learn how to review and evaluate data results · Other tasks as assigned | 7/28/2023 |
| 4349 | Alliance Pharma Malvern, PA Assistant Scientist II - Immunoassay BA/BS or higher. Exp: 1-2 years |
Responsibilities: • Prepare reagents, standards, and control samples • Analyze samples using various techniques specific to department • Perform method validation or qualification • Operate analytical equipment • Maintain analytical equipment • Ensure lab area is clean and inspection ready at all times • Remove lab waste • Record tasks in accordance with Good Documentation Practices (GDP) • Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11 • Follow applicable SOPs and procedural documents • Review and evaluate data results • Other tasks as assigned | 7/28/2023 |
| 4350 | Alliance Pharma Malvern, PA Assistant Scientist II - LCMS BA/BS or higher. Exp: 1-2 years |
Responsibilities: • Prepare reagents, standards, and control samples • Analyze samples using various techniques specific to department • Perform method validation or qualification • Operate analytical equipment • Maintain analytical equipment • Ensure lab area is clean and inspection ready at all times • Remove lab waste • Record tasks in accordance with Good Documentation Practices (GDP) • Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11 • Follow applicable SOPs and procedural documents • Review and evaluate data results • Other tasks as assigned | 7/28/2023 |
| 4351 | Allogene Therapeutics Newark, CA Associate, Cell Therapy Manufacturing (Contract) Bachelors or Associates in relevant science or engineering discipline. Exp: 0-2 years |
We are seeking a highly motivated Associate, Cell Therapy Manufacturing to join our Manufacturing team. This is a 6+ month contract role that could be extended before a decision on the full-time role is made. This role will work within the Manufacturing team in supporting our efforts in an exciting new area of cancer immunotherapy. This position is based out of Newark, CA. The position will report to the Senior Manager, Manufacturing and will support the successful tech transfer and operational readiness process, using knowledge of cGMP regulations to ensure manufacturing readiness. Responsibilities of primary importance are: to ensure the successful, time-sensitive GMP manufacture and release of cell therapy products; to follow all processes and procedures related to operations in full compliance with cGMP, CFRs, site quality systems and company policies; and to promote a culture of quality and compliance. The successful candidate will have experience in a regulated biotech or pharmaceutical setting and will have proven competency and expertise in the GMP manufacture of cell-based therapies. | 7/28/2023 |
| 4352 | Allogene Therapeutics South San Francisco, CA Associate Scientist, Analytical Development (Contract) Masters, or bachelors. Exp: 1-2 years |
We are seeking a highly motivated Associate Scientist to join our Analytical Development group and contribute to the commercialization of allogenic CAR T therapies. (S)he will play a key role in CAR T cell therapy related analytical assay development and execution of drug product release and stability assay. The individual will work closely with peers in assay development, assay qualification, execution of the release and characterization assays, comprehensive risk assessments, and data synthesis that allows for the subsequent analytical assay tech transfer. This role will be based at the headquarters in South San Francisco, CA. | 7/28/2023 |
| 4353 | Allogene Therapeutics South San Francisco, CA Associate Scientist (Contract) BSc or Msc degree. Exp: 1+ year |
Allogene is seeking a highly determined, results-oriented, self-starter who demonstrates personal accountability for outcomes and is motivated by increasing levels of responsibility, to join a dynamic team responsible for successful development and characterization of clinical-scale manufacturing of Allogeneic Chimeric Antigen Receptor T-cell therapies (Allo CAR T™). The successful candidate will help to support appropriate flow cytometry-based analytical methods for the characterization, release and stability testing of CAR T products. This position will also contribute to the development of novel technologies and approaches to meet future CAR T analytical needs and work in close collaboration with key stakeholders, including the CAR T Research and Process Development groups. This is a 1-year contract position in South San Francisco, CA. | 7/28/2023 |
| 4354 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, RNAi Discovery BS Chemistry, Biochemistry or related discipline. Exp: 0-2 years |
The RNA Synthesis team is seeking a motivated individual to join our Annealing group as an Associate Scientist II. The Annealing group is responsible for the quality control of single stranded RNA using analytical techniques such as liquid chromatography and mass spectrometry. In addition the group is responsible for formulating high quality test articles (siRNA) to support research efforts across multiple therapeutic areas. This position is onsite and will be primarily located at our 675 W. Kendall St. location in Cambridge, MA. | 7/28/2023 |
| 4355 | ALPCO Diagnostics Salem, NH Research Associate BA/BS in the Sciences. Exp: 0-3 years |
Overview of position: A successful candidate in this position will be able to multi-task and thrive in a fast-paced work environment, participate in research and development activities, and utilize established mathematical and scientific techniques to compile and analyze data. He/She will have knowledge of commonly used laboratory concepts, practices, and procedures, while relying on instructions and pre-established guidelines to perform job functions. The position requires someone with a strong work ethic, who will operate with a constant sense of urgency and commercial purpose. He/She will write technical reports detailing procedures, outcomes, and observations, can communicate and collaborate with team members, and take on additional assignments as needed. Occasional travel to scientific congresses or training may be required. | 7/28/20234 |
| 4356 | Research Associate I Jupiter, FL Research Associate I Bachelor’s Degree or equivalent in Biology, Immunology, Biochemistry, Biotechnology preferred. Exp: 1 or more years |
Alphazyme, a Maravai LifeSciences company, is looking for a Research Associate I to join our growing team. The Research Associate I supports the Company’s enzyme development projects according to internal prioritization and undertakes a variety of laboratory procedures of technical nature. This position will timely and accurately prepare various reagents, such as media, bacterial plates, and competent cells, bacterial stock maintenance, support in any area regarding enzyme expression, as well as maintenance of clean and organized laboratory space and equipment. | 7/28/2023 |
| 4357 | Research Associate Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 7/28/2023 |
| 4358 | Serotiny South San Francisco, CA Research Associate / Senior Research Associate – Cell Therapy Research Associate: BSc.; Sr. Research Associate: MSc. Exp: BSc.: 0-3 years; MSc. >2 years |
Serotiny is looking for a RA/SRA who is excited to work closely with a team of protein engineers and cell biologists to build out and deploy Serotiny's high-throughput methods to characterize and develop cutting edge therapies. The position will contribute towards the development of a novel platform to generate and characterize CAR immune cells for solid tumor indications. | 7/19/2023 |
| 4359 | SetPoint Medical Valencia, CA Quality Engineer - Temporary Position (3 - 6 months) BS in an engineering field Exp: 1+ years |
SetPoint Medical is seeking a temporary Quality Engineer to assist in the process of documenting Quality Management System (QMS) policies and procedures throughout the organization. The successful candidate must be an organized, self-motivated individual with the ability to adjust to workloads based upon the changing priorities that come with working in a fast-paced small company environment. The selected candidate will work under the Director, Quality Assurance. | 7/19/2023 |
| 4360 | Shockwave Medical Santa Clara, CA Manufacturing Engineer I Bachelor’s degree in Biomedical Engineering, Mechanical Engineering Exp: 0-3 years |
The Manufacturing Engineer I is responsible for providing engineering support to Production. The Manufacturing Engineer is also responsible for designing, developing, testing, and implementing processes, tooling, and fixtures for commercial product. In addition, the Manufacturing Engineer will work closely with the development teams developing and refining manufacturing process to ensure successful transfer into the company’s manufacturing operations. | 7/19/2023 |
| 4361 | Spark Therapeutics Philadelphia, PA Pre-Clinical Manufacturing Associate - Upstream BA/BS in biological sciences, engineering, biochemistry, or related discipline preferred Exp: 0 – 3 years |
We don’t follow footsteps. We create the path. This position is a key participant in the day-to-day operation and planning of upstream production for rAAV processes, where the production is performed with either adherent cell culture in roller bottles (up to 200 per sublot) or suspension cell culture in stirred tank bioreactors (from bench scale up to ≥ 200L). This includes production of both Research grade and GLP grade materials. Additionally, the individual will contribute to the implementation of documentation in order to support research and GLP rAAV vector manufacturing. This position requires knowledge and experience with upstream process development, including familiarity with both adherent and suspension cell culture production processes. Experience with benchtop bioreactors is a plus. Good written and verbal communication skills and ability to work effectively in a team environment are required. | 7/20/2023 |
| 4362 | Talis Biomedical Chicago, IL Senior Research Associate, Assay Development MS or equivalent in Molecular Biology, Biochemistry, Biomedical Engineering, Biochemical Engineering, Chemical Engineering, or a related field Exp: 1-5 years |
We are seeking a highly motivated, talented, and driven Senior Research Associate to join the Assay Development group in the R&D division at Talis Biomedical. This is a great opportunity to join a collaborative and dynamic team effort to enable the development of rapid point-of-care diagnostic tests. The successful candidate will work in product development, including verification and validation activities. You will author, review, and edit SOPs, study protocols, reports, and other documentation as needed. You will work collaboratively with others in Assay Development teams and other departments at Talis, including Assay Research, Operations, Quality, and Engineering. A strong understanding of nucleic acid biochemistry and experience working on cross-functional teams is highly desired. | 7/20/2023 |
| 4363 | Tevard Biosciences Cambridge, MA Research Associate, in vivo pharmacology BS/MS in Neuroscience, Physiology, Molecular/Cellular Biology, or a related Life Science discipline. Exp: 0-2 years’ |
We are looking for Research Associate (RA-I or RA-II) with an innovative mindset, great attention to detail and ability to work collaboratively to solve problems, to help advance therapeutic candidates to the clinic. The successful candidate will have an opportunity to positively impact patients with serious unmet medical needs while working closely with our world-class scientific team, including with company’s scientific co-founders. In this position, you will collaborate with the in vivo pharmacology team to study effects of therapeutic lead candidates. The RA will work with animal models for rare genetic diseases and will be responsible for executing experiments to quantify molecular, cellular, and physiological readouts, in addition to supporting in vivo dosing studies and related research activities within the in vivo pharmacology group. This is an exciting opportunity for a motivated scientist to further develop their skills in neuroscience, physiology and gene therapy while helping to make an impact on lives of patients suffering from rare diseases. | 7/20/2023 |
| 4364 | Tevard Biosciences Cambridge, MA Research Associate – tRNA and mRNA biology BS/MS in Neurobiology, Molecular/Cellular Biology, physiology, or a related discipline. Exp: 1+ years |
As an expert scientist in cellular neurobiology, you will be responsible for establishing cellular assays to demonstrate in vitro proof of concept for Tevard’s tRNA therapeutic leads and characterize the cellular activity and downstream disease-relevant biology to help prioritize candidates for in vivo studies. | 7/20/2023 |
| 4365 | Thrive Earlier Detection San Diego, CA Research Associate II Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day to day experimentation and is responsible for the execution of bench experiments and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. We are seeking a talented and highly motivated Research Associate II to join our Technology Assessment team in San Diego. The Technology Assessment group is responsible for the evaluation of novel methodologies and instrumentation to benefit Exact Sciences’ product portfolio spanning the cancer care continuum. The successful candidate will work with a small team in the evaluation of emerging technologies – including novel NGS platforms – in support of a wide variety of research and product development applications and collaborate with cross-functional teams to achieve key company objectives. This role is ideal for a driven individual with collaborative spirit and a strong background in NGS technologies and demonstrated capacity to learn quickly. | 7/21/2023 |
| 4366 | Thrive Earlier Detection Madison, WI Systems Test Engineer II/III Bachelor’s degree in engineering, computer science or related field. Exp: 1+ year |
The Systems Test Engineer II works with the Systems Development team to ensure that custom in vitro diagnostic systems meet design and customer requirements. The Systems Test Engineer II uses a technical background in software development and engineering, combined with an understanding of the system design, to analyze user needs, requirements and specifications to create testing strategies and plans for verification and validation of the system designs. | 7/21/2023 |
| 4367 | Thrive Earlier Detection Madison, WI Clinical Laboratory Science I - Contract Bachelor's degree in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution. Exp: 1+ years |
The Clinical Laboratory Scientist I performs laboratory analysis on clinical specimens using established laboratory procedures. The Clinical Laboratory Scientist I duties will include but are not limited to; processing of specimens, performance of moderate, and highly complex analytical testing, establishing, performing and documenting quality assurance, quality control, equipment maintenance, and accurately documenting all work performed under the direction of the Laboratory Medical Director. As a Clinical Laboratory Scientist I, you will recognize and resolve problems using good laboratory practices. This role is a contract position ending in March 2024. | 7/21/2023 |
| 4368 | Thrive Earlier Detection San Diego, CA R&D Laboratory Technician I Bachelor’s or Associate degree in biotechnology or field as outlined in the essential duties. Exp: 1+ years |
The R&D Laboratory Technician I is an entry level position providing support for common R&D laboratory operations functions. The position entails following detailed instructions and established procedures with frequent supervision. Responsibilities include lab organization, general lab and equipment maintenance, consumables inventory and stocking, reagent generation, and miscellaneous initiatives to help the lab run efficiently. Additionally, this position assists with sample ordering and management of both non-infectious and potentially infectious materials. The R&D Laboratory Operations Technician I is expected to follow all laboratory and safety policies, procedures, and reporting practices. | 7/21/2023 |
| 4369 | Thrive Earlier Detection Marshfield, WI Clinical Laboratory Technician - Rare Disease Sequencing Laboratory Bachelor's degree in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution. Exp: 1+ years |
The Clinical Laboratory Technician is responsible for performing standard laboratory procedures within the assigned department/laboratory. The Clinical Laboratory Technician will analyze data and may assist with research and development. This incumbent will be relied upon to follow laboratory protocols and maintain high quality levels. This role is located onsite in Marshfield, WI and works in our Sequencing Laboratory. The training for this role is 8 weeks Monday-Friday 8am-4:30pm. After training, the shift is a rotating 4-day/10-hour shift. Wednesday-Friday/Tuesday 7am-5:30pm with every 3rd weekend, 6:00am-4:30pm.The Clinical Laboratory Technician is responsible for performing standard laboratory procedures within the assigned department/laboratory. | 7/21/2023 |
| 4370 | Toxicon RTP, NC Technologist Trainee - Molecular Genetics B.A./B.S. in Biology, Chemistry, Medical Technology or relatable life science field. Exp: 0-1 year |
The Integrated Genetics Division is seeking a Molecular Technologist Trainee or Technologist to join their Molecular Genetics team in RTP, NC! The Molecular Genetics department at CMBP performs a wide array of testing for heritable disorders, including tests for cystic fibrosis, Tay-Sachs disease, Gaucher disease, fragile X syndrome, thalassemia, thrombophilia, and many more. Assays performed in the Molecular Genetics Department utilize a variety of scientific techniques, including PCR, fragment analysis, and gel electrophoresis. Participate in LabCorp’s in-house training program for the field of molecular genetics. Receive in-depth training to prepare for the ASCP-MB board exam and certification. Training program is a two year commitment, and requires signing a training reimbursement agreement. The schedule for this position will be: Tuesday – Saturday, 7am-3:30pm.The Integrated Genetics Division is seeking a Molecular Technologist Trainee or Technologist to join their Molecular Genetics team in RTP, NC! | 7/21/2023 |
| 4371 | Toxicon RTP, NC Technologist Trainee - Molecular Genetics B.A./B.S. in Biology, Chemistry, Medical Technology or relatable life science field. Exp: 0-1 year |
The Integrated Genetics Division is seeking a Molecular Technologist Trainee or Technologist to join their Molecular Genetics team in RTP, NC! The Molecular Genetics department at CMBP performs a wide array of testing for heritable disorders, including tests for cystic fibrosis, Tay-Sachs disease, Gaucher disease, fragile X syndrome, thalassemia, thrombophilia, and many more. Assays performed in the Molecular Genetics Department utilize a variety of scientific techniques, including PCR, fragment analysis, and gel electrophoresis. Participate in LabCorp’s in-house training program for the field of molecular genetics. Receive in-depth training to prepare for the ASCP-MB board exam and certification. Training program is a two year commitment, and requires signing a training reimbursement agreement. The schedule for this position will be: Sunday - Thursday, 7am-3:30pm | 7/21/2023 |
| 4372 | Toxicon RTP, NC Cytogenetics Technologist Trainee - 2nd Shift B.A./B.S. in Biology, Chemistry, Medical Technology or related life science. Exp: 0 year |
LabCorp and the Integrated Genetics Division is seeking a Cytogenetics Technologist Trainee to join their Cytogenetics team in Microarray, located in RTP, NC! Assays performed in the Cytogenetics Department utilize a variety of scientific techniques, including prenatal culturing, DNA extraction, real-time PCR, PCR, SNP microarray, and gel electrophoresis. Participate in LabCorp's in-house training program for the field of Cytogenetics. Receive in depth training and preparation for the ASCP board examination and ASCP-CG or ASCP-MB certification | 7/21/2023 |
| 4373 | Toxicon RTP, NC Cytogenetic Technologist Trainee - 2nd Shift Bachelors in Biology, Chemistry, or relatable life science field. Exp: 0+ years |
The Integrated Genetics Division is seeking a Cytogenetics Technologist Trainee to join their Cytogenetics team! Assays performed in the Cytogenetics Department utilize a variety of scientific techniques, including specimen culturing, slide preparation, and chromosome analysis. Participate in LabCorp's in-house training program for the field of Cytogenetics. Receive in depth training and preparation for the ASCP board examination and ASCP-CG certification. Training program is a two year commitment and requires signing a training reimbursement agreement. The schedule for this position will be Sunday - Thursday 1:00pm-9:30pm. | 7/21/2023 |
| 4374 | Toxicon Durham, NC Flow Cytometry Analyst Bachelors in Medical Technology or Bachelors in chemical, physical or biological science. Candidate must possess or be eligible for ASCP certification Exp: 0 - 6 months |
***** $5,000 Sign-On Bonus Offered for External Candidates ***** Integrated Oncology, a LabCorp Specialty Testing Group, provides reference anatomic pathology, hematopathology and molecular pathology testing services to hospitals, health systems and independent oncology practices. Integrated Oncology is focused on providing world class solutions to better the lives of patients living with cancer. We are offering exciting opportunities to join our team as a Flow Cytometry Analyst - Technologist in Research Triangle Park at the Center for Molecular Biology and Pathology, Durham, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". This Analyst will work alongside a highly trained staff with the latest technology. Our services are performed with the utmost care, expertise, integrity and respect for the patient. The work schedule for this position will be Wednesday-Saturday 10:00am-8:30pm, 1st shift | 7/21/2023 |
| 4375 | Toxicon Burlington, NC Technologist Trainee Bachelor's degree in Biology, Chemistry, Medical Technology or a related science, as required by CLIA. Exp: 0+ years |
$1,000 Sign-On Bonus for External Candidates Only! Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist Trainee in Burlington, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". The schedule for this position will be: 2nd shift, Tuesday-Friday, 2:00pm-12:30pm. Eligible for 10% shift differential due to 2nd shift hours | 7/21/2023 |
| 4376 | Toxicon Burlington, NC Technologist Trainee for Toxicology Bachelor's degree in Biology, Chemistry, Medical Technology or a related science. Exp: 0+ years |
$1,000 Sign-On Bonus for External Candidates Only! Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist Trainee in Burlington, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". The schedule for this position will be: 1st shift, Monday-Friday, 8:00am-4:30pm. | 7/21/2023 |
| 4377 | Trevigen Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 7/21/2023 |
| 4378 | Trevigen Minneapolis, MN Research Associate, Antibody Applications B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
The Research Associate is responsible for routine quality control testing of antibodies using immunohistochemistry (IHC) and immunocytochemistery (ICC). The testing includes culturing and handling of stem cells, primary cells, and basic cell lines for the use in ICC. The handling of fixed tissues for use in IHC. The position requires routine documentation, data analysis and good communication of results. | 7/21/2023 |
| 4379 | Trevigen Minneapolis, MN Research Associate, Analytical QC B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
As the Research Associate, Analytical Quality Control Analyst you will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include concentration determination, SDS-PAGE with densitometry, endotoxin assay, PCR, HABA, conductivity, total organic carbon and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis, and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned | 7/21/2023 |
| 4380 | Trevigen Wallingford, CT Quality Technician Bachelor of Science degree in relevant field. Exp: 0-2 years’ |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products. $22.00 to $25.00 per hour based on experience and qualifications | 7/21/2023 |
| 4381 | Trevigen Austin, TX Advanced Research Associate Master’s degree in biology, molecular biology, biochemistry, genetics, or similar fields. Exp: 0-2 years |
Advanced Research Associates in our Research Group develop innovative nucleic acid technologies. This role will support new product initiatives by combining novel, highly multiplexed PCR technologies with analysis platforms such as qPCR, digital PCR, and long-read sequencing, and by integrating reagents, instrumentation, analysis algorithms, and software. Diagnostic disease applications span neurogenetics, (such as myotonic dystrophy, fragile X and autism spectrum disorder), oncology (liquid and solid tumors), carrier screening and other reproductive health applications. You will work in a cross-functional team to develop products and technologies that realize the next generation of molecular diagnostic tests. | 7/21/2023 |
| 4382 | Trevigen Minneapolis, MN Advanced Research Associate, Stem Cell & Gene Therapy Master’s degree in a related field. Exp: up to 2 years |
The Stem Cell and Gene Therapy Advanced Research Associate will be part of a team responsible for the design and development of novel products used in cell and gene therapy workflows, including tools for expansion, identification, and differentiation of immune cells from pluripotent stem cells. Preference will be given to candidates with experience in immunology, particularly lymphocyte cell culture and/or pluripotent stem cell culture. Desirable skills and techniques include 2D and 3D cell culture and bioassays, cell separation, immunostaining, flow cytometry analysis, and molecular biology. | 7/21/2023 |
| 4383 | Trevigen Newark, CA QC Associate B.S./B.A. in molecular biology, biochemistry, cell biology or related field. Exp: 1+ years |
We seek a highly motivated and energetic Quality Control Associate to join our Operations team. This position will be working in the Quality Control team with a focus to conduct stability studies testing and support all product testing activities from raw material to finish good product. Seeking a professional associate with the ability to learn new techniques quickly and be able to adapt to shifting priorities in a fast-paced and growing environment, while adhering to established protocols and procedures. All activities will be in compliance to ISO 13485/GMP requirement. | 7/21/2023 |
| 4384 | Tyber Medical Bethlehem, PA Quality Engineer /Senior Quality Engineer Bachelor’s Degree in Engineering or Related Science field preferred Exp: 1+ years |
The Quality Engineer or Senior Quality Engineer supports Quality Management System elements across the organization, including but not limited to the following areas: Document Control, CAPA, Control of Nonconforming Material, Quality Events, Process Validation, and more. | 7/21/2023 |
| 4385 | Universal Cells Seattle, WA Research Associate II, Core Technologies, Cell Analytics MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the further molecular engineering for our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to develop molecular and cellular assays to characterize our proprietary Universal Donor Cells. | 7/21/2023 |
| 4386 | Universal Cells Seattle, WA Research Associate II, R&D MS Degree Exp: 0-2 years |
The primary purpose of this position is to conduct studies evaluating the phenotype and function of human immune cells. This will encompass both in vitro characterization of human T cells and antigen-presenting cells, as well as functional assay development to characterize pluripotent stem cell-derived immune cells. | 7/21/2023 |
| 4387 | Universal Cells Seattle, WA Research Associate II, Core Technologies MS degree in related scientific discipline Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the further molecular engineering for our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to develop molecular and cellular assays to characterize our proprietary Universal Donor Cells. | 7/21/2023 |
| 4388 | Vivex Biologics Miami, FL Quality Assurance Inspector I Bachelor degree in Life Sciences or equivalent required. Exp: 1-2 years |
The Quality Assurance Inspector is responsible for executing on a comprehensive and effective internal auditing program compliant with Standard Operating Procedures in addition to FDA, AATB, and State regulations and standards. This role also performs routine checks and verifications of the different elements of the quality system to ensure the Operation is meeting the company’s quality standards. | 7/21/2023 |
| 4389 | Frontage Hayward, CA Research Assistant- Bioanalytical Services B.S. degree in related scientific discipline. Exp: 0-3 years |
1) Assist lab work and method development 2) Follow SOP and protocol to conduct method validation and sample analysis under supervision 3) Comply with GLP regulations in lab work and documentation 4) QC review data and reports 5) Perform instrument setup, maintenance, and basic trouble-shooting under supervision 6) Strictly follow SOPs and regulations to serve as sample coordinator. | 7/21/2023 |
| 4390 | Frontage Exton, PA Lab Technician Bachelor’s degree in molecular biology, Biology, Biochemistry, Chemical Engineering, Mechanical Engineering. Exp: 1-5 years |
We are looking for a qualified Lab Technician to join our team. The role will perform and support laboratory procedures and controls within Biologics, Gene, and Cell Therapy (BGC) Department to maintain efficiency and compliance for the laboratory. The ideal candidate needs to have an entrepreneurial spirit that enables her/him to wear multiple hats as we scale-up the laboratory business. The candidate will have experience in working in a laboratory environment, preferably within biologics/or GCT lab. The candidate will be well-trained to maintain safety conditions in the lab and expected to be passionate in working in a matrix organization environment. The goal is to optimize lab compliance and maintaining the smooth running of the lab. | 7/21/2023 |
| 4391 | Frontage Secaucus, NJ Lab Technician Associate or bachelor’s degree in a biomedical discipline or related scientific discipline, or equivalent experience, or completion and certification Exp: 1 year |
Responsible for working under the guidance of the Lab Manager, Investigators; Management, Study Coordinator and Supervisor, to perform study procedures required in clinical studies conducted on behalf of sponsors at the Frontage Clinical Services. | 7/21/2023 |
| 4392 | Frontage Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 7/21/2023 |
| 4393 | Frontage Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree Exp: 0-3 years |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 7/21/2023 |
| 4394 | Frontage Hayward, CA Research Associate M.S. degree in related scientific discipline. Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 7/21/2023 |
| 4395 | Frontage Concord, OH Entry Level Lab Chemist B.S. in a chemistry or related field. Exp: entry level |
This position is for an entry level lab chemist. The ideal candidate will help support studies of preclinical drug development in a GLP environment. The duties and responsibilities include: Familiarity with a majority of laboratory equipment• Basic math and chemistry skills to perform routine calculations• Strong attention to details Perform routine lab operations in a neat and clean organized manner: prepare reagents, weigh reference standards, and extract samples Shipping, receiving, proper storing, organizing, and inventory maintenance including chain of custody documentation of new test articles. Method development and troubleshooting of formulations in conjunction with Study Directors, including conducting pH, solubility, homogeneity and stability tests Document results and accurately record observations in accordance with GLPs and SOPs Conducting pH, solubility, homogeneity and stability tests The candidate should have a good chemistry background. Excellent written and oral communication skills, and the ability to manage multiple projects in dynamic environment is highly desirable. Familiarity with regulatory guidelines (GLP or GMP) is a plus. | 7/21/2023 |
| 4396 | A2 Biotherapeutics Agoura Hills, CA Manufacturing Associate Bachelor’s Degree in Biology and/or Life Sciences. Exp: 1+ years |
A2 is seeking a highly motivated Manufacturing Associate to join the team reporting to the Manufacturing Senior Associate. In this role you will work in a dynamic production environment to manufacture T cell products for clinical and launch activities. We are looking for a strong team player who wants to help us create a high performing, collaborative work environment and deliver our innovative therapies to patients. If you are seeking an opportunity that fosters growth and challenge, apply now! This is an onsite position on a 4/10 schedule at our facility in Agoura Hills, California. | 7/21/2023 |
| 4397 | Abbott Columbus, OH Associate Scientist II - Columbus, OH Bachelor's Degree required. Exp: 1-3 years |
We currently have an Associate Scientist II position open in our Columbus, OH office. The Associate Scientist II is an individual contributor that works under limited supervision. Applies subject matter knowledge; requires capacity to understand specific needs or requirements to apply skills/knowledge. Carries out fundamental or applied research in the biological or physical sciences or in mathematics requiring appreciable originality and ingenuity. | 7/21/2023 |
| 4398 | Myriad-RBM Austin, TX Laboratory Associate - Automation Bachelor’s Degree in Chemistry or a related field. Exp: 1 year |
SHIFT - MONDAY - FRIDAY 1:30PM - 10:30PM (SHIFT DIFFERENTIALS APPLY) PURPOSE Responsible for routine sample preparation duties inclusive of automated liquid handling, troubleshooting routine experiments and the preparation of solutions. | 7/9/2023 |
| 4399 | Myriad-RBM Austin, TX Associate Scientist, Assay Development - R&D Bachelor's Degree Bachelor's degree in relevant scientific discipline (some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical Exp: 1 year |
The Associate Scientist for Assay Development is responsible for assisting with experimental execution in support of assay/method development programs. | 7/9/2023 |
| 4400 | NAMSA Northwood, OH Microbiology Technologist Bachelor degree Exp: 0 years |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. • Accurately collects and records raw data in logbooks and on worksheets. • May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. • May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. | 7/9/2023 |
| 4401 | NAMSA Northwood, OH Analytical Services Lab Technologist Bachelor’s degree in scientific discipline required. Exp: 0 years |
For bio/analytical applications, performs a variety of laboratory techniques including sample weighing and recording, preparation of standard solutions, buffers, sample preparation requiring homogenization, liquid-liquid extraction, filtration, centrifugation and pipetting, etc. • Validates bio/analytical methods and protocols adhering to GLP guidelines. • May perform routine test article/product preparation according to work instructions. • Assure testing/test article preparation/product is performed within due dates. • May prepare and maintain reagents and/or test articles as required for testing. • Performs the extraction process on prepared samples as directed by study protocol for analytical data generation. | 7/9/2023 |
| 4402 | NAMSA Minneapolis, MN Laboratory Technician An Associate or Bachelor degree in related scientific field is required. Exp: 0 years |
• Conducts sample preparation for Sponsor materials as directed by study protocols for in vivo and in vitro biocompatibility assays and pharmacology, toxicology and analytical studies. • Performs the extraction process on prepared samples in accordance to ISO, USP and JMHLW regulations as directed by study protocols for biocompatibility assays. • Receives and logs Sponsor materials for testing. Completes chain of custody documentation for test article tracking. • Prepares and maintains sterile glassware for the sample preparation process. Processes glassware through washer, autoclave and depyrogenation oven as needed. • Operates, cleans and maintains incubators, autoclaves, hoods and other equipment routinely utilized.• | 7/9/2023 |
| 4403 | NAMSA Northwood, OH Chemist Master’s degree. Exp: 0 years |
• Operates and maintains a variety of chromatographic and spectroscopic systems such as LC, LC/MS/MS, and GCMS to analyze biological and chemical elements as directed by assays or study protocols. • May order and/or stock supplies subject to approval. Maintain ancillary records (logbooks, worksheets). • Conduct routine studies independently according to work instructions. May be requested to conduct more involved studies. Routes all excursions or unusual testing occurrences to management. • Participate in the improvement of documents, test systems, quality systems, and workflow. • Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and taking all concerns to management as required. • Assure testing/test article preparation/product is performed within due dates. • For bio/analytical applications; performs a variety of laboratory techniques including sample weighing and recording, preparation of standard solutions, buffers, sample preparation requiring homogenization, liquid-liquid extraction, filtration, centrifugation and pipetting, etc | 7/11/2023 |
| 4404 | NJ Biopharmaceuticals Princeton, NJ R&D - Bioconjugation B.S. in Biochemistry, Protein Chemistry, or other related fields. Exp: 0-3 years’ |
Associate Scientist Job Responsibilities Under department supervision, plan, setup, monitor and purify bioconjugation reaction using aseptic techniques; characterize and identify bioconjugates using LC-MS, HPLC and/or Capillary Electrophoresis; maintain a detailed lab notebook; maintain equipment, and provide lab support; provide data in a detailed report; Plan and execute daily and weekly schedule; perform safe lab practices; comply with Site safety protocols and Site Standard Operating Procedures (SOPs). Perform additional duties as required. | 7/12/2023 |
| 4405 | NJ Biopharmaceuticals Princeton, NJ Associate Scientist, Process R&D, Chemistry B.S. in Chemistry. Exp: 0-5 years’ |
Job Responsibilities Support Senior and Principal Scientist – In hands-on scalable processes in kilo-lab for manufacturing pharmaceutical intermediates and Active Pharmaceutical Ingredients (APIs) and highly potent APIs (HPAPIs) after training with supervision For safely optimizing synthetic organic chemistry processes for scale up into large glassware, pilot plant tech transfers projects for APIs, and HPAPIs under supervision Running samples for characterization on NMR, MS, HPLC In pilot scale purifications using Teledyne ISCO purification and Torrent system Carry out literature searches and mine information for ongoing work from search Maintain equipment, chemical inventory, and provide lab support Execute daily and weekly tasks assigned Perform safe lab practices; comply with Site safety protocols and Site Standard Operating Procedures (SOPs) Maintain a detailed lab notebook Perform other duties as required | 7/12/2023 |
| 4406 | Oakwood Labs Oakwood Villiage, OH Chemist Bachelor’s degree in chemistry, biology, or related discipline. Exp: 0+ years |
Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development.Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development.Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for e | 7/13/2023 |
| 4407 | Oakwood Labs Oakwood Villiage, OH Chemical Engineer/ Biomedical Engineer Bachelor of Science, Masters, or PhD Degree in Biomedical or Chemical Engineering, or Chemistry or closely related science field with chemistry and ma Exp: one year |
This is an excellent entry-level opportunity for those interested in working at a technology-based pharmaceutical company. The successful incumbents will work in our product development function and: Perform pre-formulation laboratory experiments and studies Perform process scale-up from laboratory to pilot laboratory Perform process scale-up from pilot laboratory to manufacturing facility Work on technology transfer activities. | 7/13/2023 |
| 4408 | Patheon Lexington, MA Process Engineer I Bachelor’s degree in Mechanical, Chemical, Biochemical/Biomedical, Electrical, or Automation Engineering, or related field of study Exp: 1 year |
DUTIES: Support the manufacturing operations team to optimize overall equipment efficiency. Support the procurement of new systems, oversee FATs, SATs and Qualification of these new systems, layout configuration for new clients, and PFD development and equipment readiness for tech transfers. Execute process equipment improvement projects stemming from process changes/optimizations, CAPAs, and new capacity demands including compliance item. Drive continuous improvement and operational excellence culture through self-detecting and self-correcting processes and systems and instilling strong ownership and accountability. Ensure high levels of communication with team, support resources, and management regarding issues and resolutions. | 7/14/2023 |
| 4409 | Patheon Asheville, NC Engineer II, Mechanical Master’s degree in Mechanical Engineering, or related field of study. Exp: 1 year |
DUTIES: Develop specifications for system-level, subsystem and component performance based on customer needs and product requirements. Develop the optimal design through Computer Aided Engineering (CAE), Tradeoff Analysis, Technology Assessment, Failure Modes and Effects Analysis (FMEA). Develop and execute test plans to validate the performance of newly developed products by utilizing design for reliability tools and performance sensitivity analysis. Support manufacturing to evaluate and troubleshoot issues and recommend solutions to maintain production uptime. Work with Regulatory Affairs team members to design products that meet and acquire the required global product approvals and certifications such as, FDA, UL, CE, CSA, NSF, and Energy Star. Identify and implement design changes that improve user experience, quality, manufacturability, serviceability and sustainability of CTT products. | 7/14/2023 |
| 4410 | Patheon Lexington, MA QC Scientist I Bachelor’s degree in science required ; preferably Microbiology or Biology Exp: 1 year |
Location: Lexington, MA Shift: Days Wednesday-Saturday (10 hour shift) (Training will be conducted Monday -Friday between 8:00am-5:00pm) How you will make an Impact... The QC Microbiology Scientist I will be an integral member of the group in the cGMP compliant QC Microbiology Laboratory supporting manufacture of biological products. The key focuses will be to assist in the timely completion of in-process and release testing of clinical and commercial grade biopharmaceuticals, qualification/validation of analytical methods for support of viral vector cGMP compliant manufacturing and the transfer and validation of methods from clients. The incumbent will act as an analyst in the lab by performing and providing support for functional aspects of the facility such as environmental monitoring (EM), microbiological testing (bioburden, bacterial endotoxin testing, growth promotion, biological indicators, stock cultures), media fills, water testing and validation support. The incumbent will be expected to write and technically interpret controlled documents and reports, and review data produced by self and initiate investigations | 7/14/2023 |
| 4411 | Patheon San Francisco, CA Cell Therapy Specialist Bachelor’s or Associates degree in a technical field desired. Exp: 1+ years |
Apply all available resources to achieve the department goals. Take accountability for results and responsibility for the decisions made during all shifts. Hence, must ensure that the role is clear Execution of manufacturing batch records, work instructions and/or SOPs on a day-to-day basis and a focus on proactive ‘right the first time’ executions. Assist with batch record reconciliation and timely documentation. Performance of all manufacturing activities in clean room (ISO 7) environment with specialized sterile gowning. Execution of cell manufacturing and cell processing activities in closed systems and maintaining aseptic technique during processing to ensure highest integrity, viability and sterility of cellular product until release. Work as a part of the team to execute all necessary GMP runs for cell manufacturing in an accurate and timely manner Perform accurate and error-free calculations of cell concentrations, cell and media dilutions and cell viability throughout the entire cell manufacturing process workflow. Able to execute all Department functions, such as maintaining suite, supplies, equipment, logbooks and data in accordance with site SOPs and policies. Documentation of all activities to meet cGMP requirements. Execute document reviews and revisions. Daily record review, tasks, and databases. Actively provide feedback. Perform timely consumption of materials and completion of quality documentation in appropriate systems | 7/14/2023 |
| 4412 | PCI Pharma Services Bedford, NH Formulation Technician I (Wed to Sat 6 AM to 4:30 PM) BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred. Exp: 1-2 year’s |
This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. | 7/14/2023 |
| 4413 | PCI Pharma Services Bedford, NH Formulation Technician I (Sun-Wed, 6:00 AM-4:30 PM)-3 BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred. Exp: 1-2 year’s |
This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. | 7/14/2023 |
| 4414 | PCI Pharma Services Bedford, NH Plant Engineer l BS in Chemical, Mechanical, or other Engineering degree from an accredited university. Exp: 0-2 years’ |
The Plant Engineer I provides engineering support throughout the various manufacturing facilities in areas such as process equipment improvements, technological advancements, capital projects, existing manufacturing equipment, cost improvements, facility maintenance, safety and environmental regulation. Demonstrate good engineering, effective collaboration, partnering and teamwork skills when interacting with internal and external resources. | 7/14/2023 |
| 4415 | PCI Pharma Services Madison, WI Formulation Technician II BS degree in related field of study is preferred. Exp: 1 year |
This position will have the primary responsibility for daily formulation activities to ensure scheduled activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. | 7/14/2023 |
| 4416 | PCI Pharma Services Madison, WI Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 7/14/2023 |
| 4417 | PCI Pharma Services Philadelphia, PA Process Engineer Bachelor's Degree in Mechanical or Packaging Engineering or related field Exp: 1-5 years |
The Process Engineer is responsible for identifying and mitigating packaging issues for existing business through strong engineering and process improvement methods. Provide technical leadership for new product launches. Lead continuous improvement activities. Secondary tasks include specify, purchase, and commission new equipment and manage capital finances. Provide technical support for new business (Sales/Business Development Support). All activities are focused around technical and operational support to the production, maintenance, and support staffs in the areas of process improvement, equipment modification and optimization, safety, and quality improvement, and increasing throughput. This is achieved through individual effort and facilitation of teams, tracking and analysis metrics, strong understanding and utilization of good engineering practices, project management, and the use of Lean Six Sigma techniques. Additionally, the Process Engineer will be responsible determining staffing, equipment needed, equipment purchase, equipment installation, component layout and line layout | 7/14/2023 |
| 4418 | PCI Pharma Services Philadelphia, PA Process Engineer I-2nd Shft Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. As a process engineer, you will provide technical leadership for new product launches and lead continuous improvement activities. Secondary tasks include specify, purchase, and commission new equipment, manage capital finances, and provide technical support for new business (Sales/Business Development Support). All activities are focused around technical and operational support to the production, maintenance, and support staffs in the areas of process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. This is achieved through individual effort, facilitation of teams, tracking analysis metrics, strong understanding and utilization of good engineering practices, project management, with the use of Lean Six Sigma techniques. The process engineer should also have excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout | 7/14/2023 |
| 4419 | KARL STORZ Endoscopy-America Franklin, MA Project Engineer BS Degree in a Technical / Engineering discipline. Exp: 1+ years |
The purpose of this position is to develop processes to enable KARL STORZ to manufacture products with specific focus on injection molding and manual/semi-automated assembly techniques. This position will ensure the relevant infrastructure, equipment, tooling & fixturing is designed, implemented and qualified to help introduce new products and processes. | 7/14/2023 |
| 4420 | KARL STORZ Endoscopy-America Charlton, MA Test Engineer II MS degree in Electronics Technology/Engineering or related field. Exp: 0-3 years |
Under minimal supervision, provides design verification support for Karl Storz products to verify that they meet quality standards, including the design and execution of approved verification procedures, the execution of studies and troubleshooting in support of design engineering, and the training of other test engineers. | 7/14/2023 |
| 4421 | KARL STORZ Endoscopy-America Goleta, CA Test Engineer II-Contract Temporary MS degree in Electrical Engineering, Mechanical Engineering, Software Engineering, Computer Engineering, Biomedical Engineering, or related field. Exp: 0-3 years’ |
Design Verification Test Engineer II (temporary – 1 year) Shift: Mon - Thur, 10 hour Day. As a member of the Design Verification team in Goleta, CA, the Test Engineer II position holds key responsibilities for ensuring KARL STORZ’s line of video imaging systems continue to maintain their reputation among surgeons and medical staff for delivering world-class quality. Please note that this is a temporary position to support a large development project. | 7/14/2023 |
| 4422 | Agen Tus Therapeutics Lexington, MA Manufacturing Associate, Cell Therapy Bachelor’s Degree in Life Sciences or related Engineering field Exp: 1-3 years |
· Prepare equipment and materials including Clean-Out-of-Place and Sterilization. · Operate and monitor manufacturing equipment for production of biological products under minimal supervision. · Execute routine and complex production processes including, but not limited to, cell isolation, expansion, stimulation, harvest, and final fill operations. · Perform responsibilities according to procedure while maintaining compliance and safe operating practices. · Ability to troubleshoot and think innovatively to resolve process issues. · Receive and distribute supplies and maintain inventory in the Manufacturing area. · Provide feedback to supervisor on recommendations for procedural and process improvements. · Utilize process knowledge to influence positive change during the review and revision of Standard Operating Procedures (SOP’s) and Batch Records. · Maintain documentation according to current Good Manufacturing Practices (cGMP’s).· | 7/14/2023 |
| 4423 | Agen Tus Therapeutics Lexington, MA Senior Research Associate/Associate Scientist, Immuno-oncology MSc in fields such as biochemistry, molecular biology, immunology, cancer biology, or related discipline is required. Exp: 1+ years |
The successful candidate will have a strong background in cell biology, immunology, molecular biology, and/or oncology research. He/She will work closely with discovery scientists to advance research stage programs into early clinical development in the field of cancer cell therapy/immunotherapy, providing both scientific and technical expertise. | 7/14/2023 |
| 4424 | PolyPeptide Group Torrance, CA Production Chemist I BS in Chemistry, Biochemistry, Biology or related science field Exp: 1+ years |
Production Chemist is responsible for completing tasks & assignments in accordance with established processes & methodologies; synthesize peptides, intermediates, & processing from initial stage. | 7/14/2023 |
| 4425 | Prominex San Diego, CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
Prominex Inc. is a startup molecular diagnostic company with an experienced team of passionate and energetic scientists driven to create fast and affordable molecular diagnostic solutions across the globe. We are focused on infectious disease assays in point-of-care and home-based settings. We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 7/14/2023 |
| 4426 | Psomagen Cambridge, MA or Rockville, MD, MA CES Lab Technician (MD or MA) Bachelor’s degree required. Biology majors or relevant major are preferred. Exp: 1+ years |
Psomagen, Inc. is a fast-growing biotechnology company with a focus on DNA sequencing. We are currently searching for a motivated Lab Technician who is able to work full-time at our branch in Rockville (MD) or Cambridge (MA). It is the responsibility of the laboratory technician to perform routine tests using laboratory equipment. Paid training will be provided but the job requires knowledge of basic science to learn techniques/methods. It is important that the technician also understands the role of senior lab members and is able to accept constructive guidance. This role will be based in our lab in Rockville, Maryland or Cambridge, Massachusetts | 7/14/2023 |
| 4427 | Psomagen Cambridge, MA or Rockville, MD, MA Clinical Lab Scientist [MD or MA] Bachelor’s degree required. Biology majors or relevant major are preferred. Exp: 1+ years |
Psomagen, Inc. is a fast-growing biotechnology company with a focus on DNA sequencing. We are currently searching for a motivated Clinical Lab Scientist who is able to work full-time at our branch in Rockville (MD) or Cambridge (MA). It is the responsibility of the Clinical Lab Scientist to perform routine tests using laboratory equipment. Paid training will be provided but the job requires knowledge of basic science to learn techniques/methods. It is important that the Clinical Lab Scientist also understands the role of senior lab members and is able to accept constructive guidance. This role will be based in our lab in Rockville, Maryland or Cambridge, Massachusetts. | 7/14/2023 |
| 4428 | Psomagen Rockville, MD NGS Laboratory Technician/Scientist/Manager Bachelor’s degree required. Biology majors or relevant major are preferred. Exp: 1+ years |
We are looking for a meticulous clinical laboratory lab technician/associate/scientist to join our team at our NGS (next-generation sequencing) lab team. An ideal candidate will be able to perform laboratory tests, experimental procedures and effectively monitor lab inventory supplies as well as equipment. This position will be based in the Psomagen office in Rockville, Maryland (on-site). | 7/14/2023 |
| 4429 | RayzeBio Indianapolis, IN Quality Control Chemist MS in Chemistry, Science, or relevant field Exp: 1+ years |
Reporting to the Sr. Manager of Quality Control, the Quality Control Chemist will help support the establishment of a new Quality Control laboratory which supports RayzeBio’s Radiopharmaceutical manufacturing facility in Indianapolis. The Quality Control Chemist will be responsible and/or providing support for the installation, commissioning, qualification, and validation of analytical and radiochemical equipment for the QC lab. Upon establishment of the laboratory and program, this position will utilize a wide range of analytical and radiochemical analyses to support the advancement and release of novel targeted radiopharmaceuticals from the R&D phase through clinical development to GMP commercial radiopharmaceutical production. Specifically, the quality control chemist will support the release of manufactured radiopharmaceuticals to support RayzeBio’s clinical and commercial programs. | 7/14/2023 |
| 4430 | Resilience Alachua, FL Quality Control Analyst I Bachelor's Degree Exp: 1+ years |
Performs simple/compendial assays Supplies inventory and lab organization In-process and finished product samples to include bioburden, bacterial endotoxin, and sterility. Raw material testing for specific microbial requirements. Environmental Monitoring of cleanrooms and dynamic processes including viable air sampling, surface sampling, non-viable air sampling, and personnel monitoring. Sampling and analysis of purified water, Water for injection and clean steam. Sampling and analysis of compressed air and gases. Biological indicator receipt, issuance, and analysis. Media fill inspection Growth promotion of media and media fill units. Perform microbial identifications, evaluating and interpreting results to identify objectionable organisms from environmental monitoring and product testing. Demonstrate the ability to understand and interpret test results and use the results to make a decision with regard to acceptance of the associated criteria and requirements. | 7/14/2023 |
| 4431 | Resilience Waltham, MA Senior Research Associate, Upstream Process Development, Biologics Masters Degree Exp: 1+ years |
RESILIENCE is seeking a talented Sr. Research Associate in Upstream Process Development for the Biologics Franchise who will: Function as a key member of the Upstream Process Development group in Waltham, MA Focus in fed-batch and perfusion bioreactor operations Assist in building out and leading upstream operation of the Pilot lab to enable Tox Lot production Work collaboratively with other leaders throughout the network to advance objectives, priorities, and disruptive technologies Operate with the mission to transfer and develop robust, scalable, cost-effective therapeutic upstream bioprocesses for RESILIENCE Biologics partners and drive development and implementation of innovative internal technology platforms | 7/14/2023 |
| 4432 | Rocket Pharmaceuticals Cranbury, NJ Research Associate I, Nonclinical R&D B.S. in relevant Biological Sciences field Exp: 1-2 years |
Rocket is seeking an individual who will work within the R&D team supporting nonclinical studies to further understand and characterize viral vector constructs for potential therapeutic application in support of Rocket’s gene therapy pipeline. The ideal candidate will have a strong Molecular Biology background, will be highly collaborative, and will adhere to established processes, policies, and quality systems for conducting experiments and reporting data from basic research studies. This is an exciting opportunity to actively contribute to ongoing translational research efforts aimed at developing potential therapeutics for life-threatening diseases utilizing gene therapy. | 7/14/2023 |
| 4433 | Rocket Pharmaceuticals Cranbury, NJ Associate Scientist, Quality Control BS in Biology, molecular biology, virology, Life Sciences or equivalent Exp: 0 - 2 years |
We are seeking an Associate Scientist, Quality Control with the responsibility to support clinical manufacturing of a range of Gene Therapy products. Technical proficiency in analytical methodology for drug substances and drug products is required for gene-based products. | 7/14/2023 |
| 4434 | Sanaria Rockville, MD Research Associate, Cell Culture BS in biology, biotechnology, microbiology, or a related discipline Exp: 1-2 years |
We are currently seeking a Research Associate (BS) with cell culture experience to join our Gametocyte Production group. The Research Associate will be involved in many aspects of Sanaria’s PfSPZ vaccine research and cGMP manufacturing process. Ability to work on the maintenance of malaria parasite cultures and multiple simultaneous tasks is essential. The RA will participate in research projects targeted to efficiency and scaling up. The selected candidate must have weekend availability for some projects. | 7/14/2023 |
| 4435 | Sanaria Rockville, MD Research and Manufacturing Associate, Mosquito and in-Vitro Production Bachelor’s degree in biology, chemistry, biotechnology, entomology or a related field. Exp: 1+ years |
We currently have an opening for a Research Associate or Sr. Research Associate in our Mosquito and in-Vitro Production group. The Research and Manufacturing Associate will maintain cells in culture, use 3D culture, fluorescent staining methods and standard membrane feeding assays, etc. The Associate will also be required to perform key operations during PfSPZ Vaccine manufacture that will include microscopic assessments of sporozoite attenuation or enumeration, sporozoite hepatocyte invasion assays, and also mosquito production, mosquito dissection, or other component procedures. The Associate will conduct research towards malaria parasite’s sporogonic development in vitro and in mosquitoes, | 7/14/2023 |
| 4436 | SCA Pharma Windsor, CT Chemist I Bachelor’s degree in Chemistry, Biology, Chemical Engineering or Life Sciences (Preferred in Chemistry). Exp: 1+ years |
The Quality Control (QC) Chemist I is an entry level position for individuals who use their understanding of Analytical Chemistry to perform the basic and routine experiments including generation and analysis of data in a cGMP laboratory. | 7/14/2023 |
| 4437 | SCA Pharma Little Rock, AR Incoming Quality Assurance (IQA) Specialist Bachelor’s degree in life sciences, engineering, or related discipline preferred Exp: 1+ years |
The Incoming Quality Assurance Specialist will ensure that critical and key raw materials and supplies that are received meet raw material specifications set forth by SCA Pharmaceuticals and have appropriate certificates of analysis and certificates of conformance prior to releasing to inventory. These responsibilities will be performed at the production site as well as the warehouse site. In addition, the individual in this position will be responsible for maintaining and improving existing processes, as well as assisting in the design and development of new processes, in the areas of Incoming Quality Assurance release requirements, trending of received material specifications, assisting with recalls of raw materials, assisting with raw material specification creation, and coordinating raw material specification changes. | 7/14/2023 |
| 4438 | PerkinElmer Pennington Reserve at Upper Provide, PA Research Technician Bachelor’s Degree in a scientific field. Exp: 1+ years |
Job Responsibilities: Weekly liquid nitrogen filling of NMRs Perform morning startups of NMRs Perform equipment user-level upkeep, minor troubleshooting, general laboratory prep work, inventory checks, and scheduled equipment quality checks. Notifies supervisor and/or manager when deficiencies are noted. Participate in audits and inspections and provide input, as requested. Support general technical lab activities as needed (ex: replacing water in water baths / incubators, removing expired chemicals in the lab, ensuring that filters are changed on freezers, etc.) Maintain training and compliance in areas of health and safety, security, environmental and operational aspects of daily activities in the working environment | 7/3/2023 |
| 4439 | PerkinElmer Annapolis, MD Research Specialist Bachelors Degree in science or chemistry. Exp: 6 months |
Responsibilities: Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. Perform established flow cytometry QC protocols on a routine basis and analyze results. Generate and analyze data with the highest Data Integrity standards to include identifying and reporting unusual results/outcomes. Operate and maintain laboratory instrumentation including Mycoplasma onsite testing & clean-up as warranted. | 7/3/2023 |
| 4440 | PerkinElmer Annapolis, MD Media Prep Specialist Bachelor’s Degree in a chemistry, biology, or other relevant discipline. Exp: 1+ years |
Responsibilities: Prepare high quality media, buffer, and reagents according to a regularly occurring schedule as well as special requests. Track & document shelf life of media mixes, and plan for re-occurring mix preparation Follow SOPs, protocols, and other guidelines as it relates to the preparation of reagents and buffers Quality control testing of these materials to ensure products are free of contaminations and are formulated appropriately Maintain relevant lab supplies and materials, manage stock solutioninventory and prepare as needed Write, maintain, and troubleshoot experimental protocols Analyze, synthesize, and communicate data to both technical and non-technical colleagues and collaborators Be able to interact with colleagues in other functions and department to solve technical problems Perform general laboratory tasks, which may includeupkeep of equipment, stocking of consumables, glass washing, and overall lab upkeep Proficient technical skills required upon completion of relevant training: balance usage, pH meters, liquid-transfer devices | 7/3/2023 |
| 4441 | Sanofi Waltham, MA mRNA -Senior Research Associate, Purification (Plasmid Production) - Vaccine MS in biochemistry, chemistry, chemical or biomedical engineering. Exp: 0-2 years |
We are seeking a highly motivated and scientifically rigorous individual to join the Plasmid Production Pilot team. You will focus on execution and scale-up of a robust pDNA production process focusing on bacterial cell lysis, supercoiled plasmid DNA linearization, and purification for preclinical linearized plasmid DNA production, with the ultimate goal of transferring at scale methods to either the internal or external manufacturing team for mRNA drug substance with applications towards vaccine development. Evaluate and implement purification technology and optimize existing techniques and workflows. Support the execution and optimization of plasmid DNA purification, problem solving. Design and execute decision-quality research; prepare/draft SOPs, technical reports, batch record, and presentations to management and other stakeholders. Work independently, pro-actively, and be an impactful contributor to project teams. Function in highly collaborative cross functional teams. Execute ~20 batches per year. | 7/4/2023 |
| 4442 | Sanofi Waltham, MA mRNA -Senior Research Associate, Plasmid Production (Upstream Fermentation) - Vaccine MS in cell or molecular biology, biochemistry, chemical or biomedical engineering, biotechnology Exp: 0-2 years |
We are seeking a highly motivated and scientifically rigorous individual to join the Plasmid Production Pilot team. You will focus on execution and scale-up of a robust pDNA production process through fermentation, cell lysis extraction, linearization, and purification for preclinical linearized plasmid DNA production, with the ultimate goal of transferring at-scale methods to either the internal or external manufacturing teams for mRNA drug substance manufacturing team with applications towards vaccine development. Evaluate, and implement new biology and purification technology and optimize existing techniques and workflows, including the execution and optimization of plasmid production, problem solving. Execute decision-quality research; prepare/draft SOPs, batch record, and presentation to Plasmid Production Pilot team. Work independently, pro-actively, and be an impactful contributor to project teams. Function in highly collaborative cross functional teams. Execute ~20 batches per year. This will be primarily a lab-based position. | 7/4/2023 |
| 4443 | Sanofi Cambridge, MA Senior Research Associate, Dupixent Research, Immunology and Inflammation Therapeutic Area Master’s Degree Exp: 1 year |
The Type 2 Inflammation and Dupixent Research cluster in the Immunology and Inflammation therapeutic area within Sanofi is seeking an experienced and highly motivated scientist to join their team. The candidate will help to expand our mechanistic understanding of Dupixent and maximize its value through execution of dedicated research studies. A successful candidate will have a background in immunology and an ability to integrate into multiple projects, contributing technical in vitro and in vivo skills. The candidate must be driven, resourceful, and able to work independently. Excellent organizational skills in management of data, reagents and equipment are essential. The candidate will participate in regular team meetings and present results, interpret data, and formulate conclusions. Teamwork, collaboration with colleagues across disciplines and excellent verbal and written communication skills are critical. | 7/4/2023 |
| 4444 | Sanofi Cambridge, MA Senior Research Associate Immunology - Vaccines - VIE Contract (W/M) Master’s Degree in Immunology, Virology, Biochemistry or Physical Science or applied science field Exp: 1 year |
We are looking for: Senior Research Associate Immunology - Vaccines - VIE Contract (W/M) Target start date: 01/09/2023 Responsibilities: Laboratory research/Assay development/Immunomodels development With limited oversight, collaborate on project design, planning and execution of studies With limited oversight, exercise creativity when devising new protocols and/or optimizing assays for stronger performance With manager oversight, design and perform experiments that comply with SOPs and maintain scientific norms (contains appropriate positive and negative controls, replicates, standards, etc.) to appropriately achieve goals set forth in study plans Exercise knowledge in selection, design, execution, and analysis of experiments that contribute to project goals Perform a wide variety of technical procedures and operate a wide variety of lab instrumentation/computer platforms related to Immunology Support the development and optimization of automation protocols for immune assays Participate in monitoring and maintaining facility related aspects of the lab and lab equipment as needed | 7/4/2023 |
| 4445 | Siemans Healthineers Newark, DE Laboratory Technician 2-Weekend Shift Bachelor’s degree or equivalent required on one or more of the following fields: Biochemistry, Biology or Chemistry Exp: 1 year |
This is a role well suited to an ambitious professional, looking for the next step in their career. As a Laboratory Technician, you will be responsible for: • Works within Specialty Reagents In-Vitro Production team to produce antibody raw material. • Responsibilities include preparation of nutrient supplements, equipment set up, autoclave operation, as well as operating equipment that is needed to harvest and purify antibody material. • Responsible for monitoring and controlling processes while maintaining accurate quality records. • Working understanding of Windows environment and related software • Work in a control environment and complete tasks aseptically to ensure no microbial contamination | 7/5/2023 |
| 4446 | Siemans Healthineers Walpole, MA Laboratory Technicians Bachelor degree with a concentration in science (Biochemistry, Biology, Chemistry, etc.) Exp: 0-1 years |
Do you want to join us in helping to fight the world’s most threatening diseases and enabling access to care for more people around the world? At Siemens Healthineers, we pioneer breakthroughs in healthcare. For everyone. Everywhere. We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our Walpole Reagent Manufacturing team as a Laboratory Technician in: Reagent Manufacturing Technicians, QC Technicians, or QC Microbiology Technicians. | 7/5/2023 |
| 4447 | Siemans Healthineers Johnson City, TN Test Engineer, R&D - Level 1 Bachelor’s in Electrical Engineering, Computer Engineering, or Computer Science (listed in priority order) Exp: 0-3 years |
The Test Engineer participates in analyzing, developing, implementing processes, technologies, and systems for the testing of automation products. May work with hardware and software design to perform fault insertion tests or development tests of prototype products. The Test Engineer reports to the Engineering Manager / Project Leader working on Functional Safety projects and is an individual contributor working directly within the test team under the direction of the Technical Team Lead Engineer. | 7/5/2023 |
| 4448 | Siemans Healthineers Mishawaka, IN Scientist I Bachelor’s degree in a science related field, preferably chemistry or biology. Exp: 1-2 years |
This is a role well suited to an ambitious professional, looking for the next step in their career. As a Scientist 1, you will be responsible for: • Performs a wide variety of assignments according to established procedures, including but not limited routine and moderate tests/analyses, data review and analysis, as well as solution preparations • Completes preparation of product release reports • Reviews documentation generated by the lab prior to release to ensure accuracy and completeness • Provides inputs used for the purpose of control charting and trending of data collected through the release process • Ensures compliance of current procedures and processes and as needed reviews and updates documentation • Communicates issues encountered in the lab to initiate the investigation phase as well as aids in troubleshooting process with the lab supervisor | 7/5/2023 |
| 4449 | Siemans Healthineers Mishawaka, IN Scientist I Bachelor’s degree in a science related field, preferably chemistry or biology Exp: 1-2 years |
This is a role well suited to an ambitious professional, looking for the next step in their career. As a Scientist 1, you will be responsible for: • Performs a wide variety of assignments according to established procedures, including but not limited routine and moderate tests/analyses, data review and analysis, as well as solution preparations • Completes preparation of product release reports • Reviews documentation generated by the lab prior to release to ensure accuracy and completeness • Provides inputs used for the purpose of control charting and trending of data collected through the release process • Ensures compliance of current procedures and processes and as needed reviews and updates documentation • Communicates issues encountered in the lab to initiate the investigation phase as well as aids in troubleshooting process with the lab supervisor • Participation in validation activities for equipment qualifications and process implementations | 7/5/2023 |
| 4450 | Siemans Healthineers Lexington, MA Process Engineer I Bachelor’s degree in Mechanical, Chemical, Biochemical/Biomedical, Electrical, or Automation Engineering. Exp: 1 year |
Support the manufacturing operations team to optimize overall equipment efficiency. Support the procurement of new systems, oversee FATs, SATs and Qualification of these new systems, layout configuration for new clients, and PFD development and equipment readiness for tech transfers. Execute process equipment improvement projects stemming from process changes/optimizations, CAPAs, and new capacity demands including compliance item. Drive continuous improvement and operational excellence culture through self-detecting and self-correcting processes and systems and instilling strong ownership and accountability. Ensure high levels of communication with team, support resources, and management regarding issues and resolutions | 7/5/2023 |
| 4451 | Jordi Labs Mansfield, MA Chemist Master’s degree in chemistry or other closely related field. Exp: one year |
Job duties: 1) Prepare technical reports 2) Interpret gas chromatograph mass spectrometry (GCMS) and liquid chromatograph mass spectrometry (LCMS) results with a high level of proficiency 3) Interpret chromatographic data including high performance liquid chromatography (HPLC), gas chromatography (GC), and gel permeation chromatography (GPC) results 4) Combine results from multiple techniques to identify unknown chemical compounds 5) Quantify chemical components using HPLC and GC results 6) Work with a team of scientists to design and implement analytical strategies 7) Perform or oversee complex analytical strategies with an emphasis of MS and chromatography | 7/5/2023 |
| 4452 | Jordi Labs Mansfield, MA Analytical Laboratory Chemist Bachelor’s degree in Science preferred. Exp: One years |
Laboratory Tasks Sample Preparation Differential Scanning Calorimetry (DSC) Thermal Gravimetric Analysis (TGA) Gel Permeation Chromatography (GPC) Fourier Transform Infrared Spectroscopy (FTIR) Solid Phase Extraction (SPE) Preparation of Technical Reports | 7/5/2023 |
| 4453 | Kriya Therapeutics Morrisville, NC Analyst I, Quality Control Microbiology BS in Microbiology or other related field. Exp: 0 – 2+ years |
We are seeking a Quality Control (QC) Analyst I to join the QC Microbiology team at Kriya. This individual will play a critical role in the qualification of Kriya’s Manufacturing Facility, including Environmental and Compressed Gas Monitoring. In addition to, this individual will support sample control, raw material release, and microbiology laboratory testing. | 7/5/2023 |
| 4454 | Krystal Biotech Pittsburgh, PA Research Associate / Senior Research Associate, Platform Development Bachelor’s or Master’s in Biological Sciences or related scientific discipline. Exp: 1+ years |
The Platform Development group is seeking a highly motivated and innovative Research Associate or Senior Research Associate to join our multidisciplinary team. To be successful, the candidate should demonstrate basic knowledge in fundamental cloning and molecular biology techniques, tissue culture, and virology, show curiosity, initiative, and the ability to work well in a timeline-driven environment. | 7/5/2023 |
| 4455 | Krystal Biotech Pittsburgh, PA Research Associate, Analytical Development Bachelor’s degree (Biology, Biochemistry, Chemistry, or related science) Exp: 0-2+ years |
Krystal Biotech, Inc is seeking a highly motivated Research Associate to perform high quality analytical development to support research for gene therapy products. This position will be laboratory based. | 7/5/2023 |
| 4456 | Krystal Biotech Pittsburgh, PA Process Validation Associate / Engineer Bachelors’ Degree in Chemical Engineering, Biomedical Engineering Exp: Associate: 1+ yr |
Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) or Engineer (3+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site. | 7/5/2023 |
| 4457 | Krystal Biotech Pittsburgh, PA Manufacturing Sciences & Technology (MSAT) Associate Bachelor’s degree. Exp: 1+ year |
Krystal Biotech, Inc is seeking a highly motivated Manufacturing Sciences and Technology (MSAT) Associate to support technical transfer and continuous improvement of product manufacturing at our growing GMP facility. The Associate will have a critical role and operate cross-functionally in the development of our products and processes across a range of manufacturing activities. | 7/5/2023 |
| 4458 | Krystal Biotech Pittsburgh, PA Quality Control Analyst I/II Bachelor’s degree in life science required Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and detail-oriented Quality Control Analyst who will perform various assays and analytical testing for the release of drug products, for clinical and commercial use. A strong foundation in cell culture techniques will be essential to this role supporting the development, manufacturing, and release of gene therapy products. | 7/5/2023 |
| 4459 | Krystal Biotech Pittsburgh, PA Regulatory Affairs Associate Bachelor’s degree in a Scientific or related field. Exp: 1-3 years |
Krystal Biotech, Inc is seeking a highly motivated Regulatory Affairs Associate to support all regulatory activities from product development and pre-clinical through product approvals. They will play an active role in preparation of regulatory documents and ensuring submissions are quality in nature and on-time. The Associate will work onsite with the team, based in our Pittsburgh facility. | 7/5/2023 |
| 4460 | KSQ Therapeutics Lexington, MA Associate Scientist/Senior Associate Scientist, In Vivo Pharmacology BSc Exp: 1-2+ yrs |
KSQ Therapeutics is seeking an Associate Scientist/Senior Associate Scientist with an interest in discovering and advancing the next generation of cell therapies for the treatment of cancer to join the in vivo pharmacology team. Our ideal candidate thrives in a research environment that demands teamwork, scientific rigor and technical excellence. Previous hands-on in vivo experience is required. Interested people with experience in the discovery and development of NK/T cell adoptive cell therapies are strongly encouraged to apply. The ideal candidate would be able to learn additional in vivo and ex vivo activities as needed to support the progression of our immuno-oncology pipeline and engaging partnerships. They will work as part of a team to ensure delivery of key data sets as well as develop and deliver scientific presentations and reports. | 7/5/2023 |
| 4461 | LakePharma Rensselaer, NY Process Engineer I Bachelor’s degree in Biology, Chemical Engineering or related field Exp: 0-3 years’ |
The Process Engineer I will be responsible for facilitating the tech transfer of client processes and executing engineering functions including design, scale up document controls. | 7/6/2023 |
| 4462 | LakePharma Rensselaer, NY Production Technician Associates or Bachelor's degree preferred. Exp: 0+ years |
The Production Technician is an integral part of the team, contributing to our success by weighing out chemicals and preparing various types of solutions for use in process. | 7/6/2023 |
| 4463 | LakePharma Lebanon, NJ Microbiology Lab Analyst I BS in Microbiology or a related scientific discipline or MS in Microbiology or a related scientific discipline. Exp: BS: 0-2 years ; MS: 0 years |
The Microbiology Laboratory Analyst I is an integral part of the Curia team, contributing to our success by assisting in the execution and development of technical and business aspects of the Microbiology Laboratory. As the Microbiology Laboratory Analyst I you may be responsible for sample intake, performing sample analyses, and any other tasks as assigned by management. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. | 7/6/2023 |
| 4464 | LakePharma Albany, NY Research Scientist I; Medicinal Chemistry Bachelors or Masters Degree with major in chemistry. Exp: 0-5 years |
The Research Scientist I is an integral part of the Curia team, contributing to our success by the synthesis, purification and identification of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. | 7/6/2023 |
| 4465 | Liquidia Morrisville, NC Manufacturing Technician B.S. degree Exp: 0-2 year’s |
We are looking for a hands-on and experienced Manufacturing Technician. In this role, you will perform routine running of manufacturing equipment to support production and R&D efforts. Furthermore, you will provide feedback to engineering and scientific staff on process performance and ideas for process improvement. | 7/7/2023 |
| 4466 | Liquidia Morrisville, NC Associate Scientist, Quality Control Lab B.S. degree in chemistry, pharmaceutical sciences, or a similar scientific field. Exp: 0-2 years’ |
We are looking for an Associate Scientist, Quality Control Lab, located at our headquarters office. In this “hands-on” role within the Quality Control Lab, the Associate Scientist will join a talented and collaborative team that welcomes input and suggestions to help continue Liquidia’s upward trajectory at the most exciting time in the Company’s history. Critical to success are a scientific laboratory background, ability to follow CGMP documentation requirements, and excellent communication skills. The Associate Scientist will conduct laboratory analysis of raw materials and intermediates in support of Liquidia’s lead product candidate, for PH. | 7/7/2023 |
| 4467 | Lyra Therapeutics Watertown, MA MSAT Engineer I/II Bachelor’s Degree (Engineering Preferred) Exp: 1+ years |
Our team is growing, and we are currently recruiting a Manufacturing Sciences and Technology (MSAT) Engineer I/II to support pharmaceutical operations at the Waltham and Watertown, MA sites. The focus of this position is to ensure manufacturing equipment and processes are operating as intended to meet the requirements for drug product manufacturing. This position will play a key role in delivering results in a fast paced, highly collaborative, and dynamic environment. The position will assist in the startup of a combination drug-device product from new product launch through commercial production. This involves process development, commercial process validations, technology transfers, as well as being accountable for commercial production. | 7/7/2023 |
| 4468 | Mammoth Biosciences Brisbane, CA Research Associate I/II, Tx Platform Development Bachelor’s degree in molecular and cell biology, immunology, biochemistry, or a related field. Exp: 1 year |
Mammoth is hiring a Research Associate I/II to contribute to R&D projects run within the Platform team. The Platform team develops next-generation CRISPR tools for therapeutic genome editing applications and is composed of technical staff with diverse strengths in bioinformatics, biochemistry, protein engineering and high-throughput screening. The successful candidate will work on CRISPR tool development projects during their early (proof-of-concept) and/or late (optimization) phases. This is a fantastic opportunity to impact human health by making CRISPR tools that cure genetic disease. | 7/7/2023 |
| 4469 | Mammoth Biosciences Brisbane, CA Research Associate I/II/Senior Research Associate- Screening and Assay Development Bachelor’s or Master's degree in molecular biology, genome sciences, biochemistry, or a related field. Exp: 1 year |
Mammoth is currently seeking a creative and detail-oriented Research Associate with interest in translating CRISPR research into the clinic. The ideal candidate will join the assay development team to work collaboratively to execute essential workflows that support efficacy validation for many preclinical programs. The ideal candidate will be part of the screening and assay development team, which is responsible for measuring DNA, RNA, and protein from tissues and cells. These activities include measuring CRISPR induced editing events in DNA, digital PCR to measure guide and mRNA stability and distribution, and western blots and ELISAs to measure protein quantity and stability. Additionally, supports high throughput screening of CRISPR systems for different cell model systems. | 7/7/2023 |
| 4470 | Masy BioServices St. Louis, MO Associate Scientist I, Chemistry Bachelor’s degree in Pharmaceutical Sciences, Chemistry or equivalent required. Exp: 1+ years |
The Associate Scientist I is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4471 | Masy BioServices St. Louis, MO Associate Scientist I, Microbiology Bachelor’s degree Biology, Microbiology or related field. Exp: 0-2 years |
The Associate Scientist, Microbiology is accountable for driving results in a fast-paced environment by accurately and efficiently performing sample analysis, monitoring microbial cultures and identifying microbiological contaminants and pathogens using a variety of identification methods. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4472 | Masy BioServices Wilmington, NC Associate Scientist I/II Bachelor’s degree in Chemistry or related field. Exp: 0 – 4+ years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. This position may also be required to work on method development/method validation projects. Typical types of testing include: assays (potencies, related substances, residual solvents, metals etc.), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, DSC, TGA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client/vendor supplied or developed by Alcami). The Associate Scientist II must have the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data is required. The Associate Scientist II will occasionally be called upon to support and mentor other Analytical Chemists within the lab. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4473 | Masy BioServices Wilmington, NC Associate Scientist III - QC Testing Master’s degree in Chemistry or a related field. Exp: 0-5 years |
The Associate Scientist III is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also assist with method development/method validation projects. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: CKF/KF, ICP-MS, Particle Size, CCIT, UV. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4474 | Masy BioServices Morrisville, NC Associate Scientist II - Raw Materials Bachelor's degree in Pharmaceutical Sciences or Chemistry or Master's degree. Exp: BS: 1 years; MS: 0 years |
The position is responsible for support of compendial testing group and manages priorities of this team to provide the timely, compliant and accurate testing of raw materials, critical utilities, in-process samples and finished product. This position will collaborate with cross-functional teams and will work side-by-side with other scientists and professionals to drive the scientific agenda. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4475 | Mekonos Berkeley, CA Research Associate, Microfluidics B.S or M.S in a relevant engineering or scientific discipline Exp: 0+ years |
We are looking for a Microfluidics Research Associate to join us and have an impact in the following ways: Design, build and test microfluidic parts Plan and execute research operations Demonstrate high scientific integrity and reporting standards Promote a positive and exciting work environment This is an in-person role, based in Alameda, CA. You are not expected to have experience with all listed requirements. If you feel passionately about our mission and values, please consider applying. | 7/7/2023 |
| 4476 | Myriad Genetics Salt Lake City, UT Lab Tech I (myRisk Post Lab, Nights Sun-Wed 8p-6:30a) Bachelor’s degree in a chemical, physical, biological or clinical laboratory/medical technology science. Exp: 1+ years |
Responsibilities Complying with the laboratory’s technical, administrative and safety policies and procedures. Participating in the laboratory’s quality assurance plan, adhering to quality control and preventive maintenance policies and appropriately documenting these activities. Working as part of a team to produce repeatable quality results. Maintaining a clean and organized laboratory space. Following Standard Operating Procedures (SOPs). Operating high performance liquid handling robots. Participating in continuing education according to accepted laboratory standards. Actively participating in successful and timely completion of training and competency assessment as outlined in the laboratory and departmental training programs. | 7/7/2023 |
| 4477 | Myriad Genetics Salt Lake City, UT Lab Tech I (myRisk Post PCR, Weekend Nights Thurs-Sat 6pm-6:30am) Bachelor’s degree in a chemical, physical, biological or clinical laboratory/medical technology science. Exp: 1+ years |
Myriad Genetics is looking for a Lab Tech to join our myRisk PCR Post Lab Team. MyRisk with RiskScore® is a powerful tool that evaluates 48 genes to help healthcare providers identify their patients’ risk of developing 11 different types of hereditary cancer. More than a test, MyRisk’s clear, actionable results are the foundation for personalized care plans that can be used to help patients make confident, informed decisions about their medical management. The is a full-time position and the schedule for this position is Thursday through Saturday 6:00pm-6:30am MST. | 7/7/2023 |
| 4478 | Indigo Biosciences State College, PA Associate Scientist Master’s Degree in a relevant field of the biological sciences. Exp: 0+ years |
INDIGO’s Associate Scientists are bench scientists that work within a Research Team. It is expected that they will be intellectually engaged in critically evaluating experimental data, trouble-shooting technical problems, brainstorming the application of new or alternative technologies/methods, and interacting with INDIGO’s Sales and Marketing Teams, as well as directly with our customers. | 6/27/2023 |
| 4479 | Instil Bio Tarzana, CA Technician, QC Analytical Bachelor Degree Exp: 0+ years |
Instil Bio is looking for a highly motivated and driven individual to join us as a technician in the Quality Control organization. Initially as part of the start-up activities, you will be responsible for establishment and set-up of the QC testing laboratories in Tarzana area. As the site transitions into operation, you will primarily be responsible for providing technical expertise, testing and release of product, package material, raw material used in the production of Instil Bio’s cell therapy product. | 6/27/2023 |
| 4480 | Pace Analytical Maplewood, MN Lab Analyst - Rheology B.S. in Chemistry, Physics, Materials Science, Engineering or related field. Exp: 0+ years |
Join us as a Lab Technician Rheology, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. A candidate for this position should be familiar with mechanical properties testing including dynamic mechanical analysis (DMA), tensile testing, lap shear, etc. A candidate would be expected to follow standard procedures to prepare samples, set up instrumentation and run experiments and process data. A candidate will report results using previously developed standard formats. | 6/27/2023 |
| 4481 | Pace Analytical Minneapolis, MN GC LC Chemist - Analytical Instrument Specialist BS degree in chemistry or related science. Exp: 0+ years |
Instrument Services Specialists are responsible for providing technical solutions and an advanced level of instrument support services to customers of TFS, including external clients, laboratory chemists within the Pace lab system, and departmental coworkers. They also provide our customers with a variety of support services associated with their analytical instrumentation. These services include routine maintenance, operational and performance testing, hardware and software troubleshooting, instrument repair, and personnel training. | 6/27/2023 |
| 4482 | Pace Analytical Brooklyn Park, MN Microbiologist Bachelor's degree in Microbiology, Biology or a related discipline required. Exp: 1 year - 4 years |
Join us as a Microbiologist, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The main function of the QC Microbiologist is to perform supportive activities for general lab readiness, conducting critical biological tests, and following SOPs to perform methods using analytical skills and understanding of biological and chemistry techniques and principles. | 6/27/2023 |
| 4483 | Pace Analytical Greenfield, IN Microbiologist/Molecular Biologist Bachelor's degree in Biology, focus in Microbiology and Molecular Biology preferred. Exp: 1+ years |
Candidate will use their skills and knowledge in Microbiology, Molecular Biology and Bacteriology to support development of new products. | 6/27/2023 |
| 4484 | Pace Analytical Maplewood, MN Microbiologist- Food Safety BS degree in Biology, Microbiology, or related science. Exp: 0+ years |
Join us as a Microbiologist, where you’ll put your love of science to work in the Scientific Insourcing Solutions division. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This position will actively support food safety and quality assurance through the use, and validation of, pathogen detection products. The analyst will prepare and evaluate samples using aseptic technique to ensure products meet specifications. The products being monitored are crucial to maintaining consumer safe food supply chains. Work is performed as part of a team in a collaborative environment. Position may require occasional weekend shifts. | 6/27/2023 |
| 4485 | Pace Analytical Sugar Land, TX Chemical Technician 1 - Entry Level Bachelor's degree in chemistry or biology preferred. Exp: 0-2 years |
Join us as an Entry Level Chemical Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The main function of a laboratory technician is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. The chemical technician will work in an experimental lab on research and development projects including hands on wet bench chemistry, chemicals handling, preparation of solutions/dilutions as well as routine analytical characterization and data analysis. Note: This position is expected to last 1 year. | 6/27/2023 |
| 4486 | Pace Analytical Eagen, MN Scientist (Chemists, Lab Technicians) Bachelor's degree in Biology, Chemistry, Physics, and other related science. Exp: 1+ years |
Join us at Pace, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This is a lab based position. The candidate will be conducting various physical and chemical tests to assist scientists in making qualitative and quantitative analyses. Role may involve wet bench lab work, chemical handling, preparation of solutions/dilutions as well as routine analytical characterization and data analysis. Various shifts may be available. Several locations within the Minneapolis area and surrounding cities. These positions are contracted positions which may last up to 12 months. Note: This is an evergreen posting for future positions within our team. | 6/27/2023 |
| 4487 | Charles River Laboratories Watertown, MA Research Associate I 1 BS in the biological sciences or a relevant field is required. Exp: 0-3 years |
In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). The Research Associate will be responsible for accurate data entry. To ensure the success of the research projects, it is critical that you maintain accurate study records and assist in maintaining lab and facility inventories. As part of your role, you will be expected to complete study reports and perform routine animal health-related tasks such as changing cages or supplying food as needed. Your attention to detail and ability to follow procedures carefully will be essential to ensure the accuracy and reliability of your research results. Lastly, you may need to perform health rounds and treatments on weekends, holidays, and occasional evenings.In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). | 6/27/2023 |
| 4488 | Charles River Laboratories Northridge, CA Quality Control Associate AA or BS degree in Life sciences preferred. Exp: 0-2 years |
The QC Associate I supports the Quality Control Manager to maintain the Quality Control program at Cell Solutions Charles River Laboratory, Northridge. The QC Associate will be responsible for performing Quality Control testing of samples/materials generated during the manufacturing of all cryopreserved products, perform microbiological Environmental Monitoring of Cell Processing/Clinical Labs as well as activities covering the inspection, sampling and testing of incoming raw materials. | 6/27/2023 |
| 4489 | Charles River Laboratories Mattawan, MI Research Technician - Second Shift Operations *$1,000 sign on bonus *$20/hr starting wage Bachelor’s/Master’s Exp: 0 years |
We are seeking a Research Technician for our Second Shift Operations at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 6/27/2023 |
| 4490 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician 1 (Tuesday - Saturday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 6/27/2023 |
| 4491 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. This is a Monday - Friday 2:30-11:00am position.We have an exciting opportunity for a Research Technician I at our Discovery site located in Worcester, MA. | 6/27/2023 |
| 4492 | Charles River Laboratories Mattawan, MI Research Technician I- Molecular Imaging Bachelor’s/Master’s Exp: 0 years |
*$1,000 new hire sign on bonus and $20/hr starting wage Job Summary We are seeking a Research Technician for our Molecular Imaging Team located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 6/27/2023 |
| 4493 | Charles River Laboratories Mattawan, MI Research Analyst II, Discovery Bioanalytical 1 BS/BA in relevant field. Exp: 1 year |
Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 6/27/2023 |
| 4494 | Genesis Therapeutics San Diego, CA (Sr.) DMPK Research associate A Bachelor’s, Master’s or Ph.D. in Chemistry, Biological Sciences, Pharmacology or related discipline. Exp: 1-2+ years |
Genesis Therapeutics is pioneering artificial intelligence guided rational drug design to address severe unmet medical needs for patients. Our lab in San Diego is looking for a motivated and versatile Drug Metabolism and Pharmacokinetics (DMPK) Scientist or Sr Scientist to join our team to help advance our compounds through preclinical and clinical development. The successful candidate will be involved in drug discovery and development through the conduct of DMPK assays. This is a full-time position in a fast-paced biotech environment with a collegial group of high-level colleagues working towards well-defined goals. Full medical and dental benefits, flexible work hours/vacation included in this opportunity to learn all aspects of biotech start-up. | 6/28/2023 |
| 4495 | Integra LifeSciences Mansfield, MA PROJECT ENGINEER, LCM OPERATIONS Master’s degree in mechanical, manufacturing, materials or biomedical engineering. Exp: 1-3 years |
ESSENTIAL DUTIES AND RESPONSIBILITIES: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Lead and Participate on cross-functional project teams including R&D, Quality Assurance, Supplier Quality, Planning, Purchasing, Regulatory, and Manufacturing to maintain and improve surgical products. Develop project plans for qualifications and ensure team resources identified, team members help accountable to deliverables, and milestones met. Provide engineering knowledge and oversight to resolve manufacturing- and quality-related problems with existing products. Support and lead manufacturing process improvements for CSS products in both internal manufacturing facilities and in partnership with external suppliers. Provide project leadership to improve existing products and associated manufacturing processes. | 6/29/2023 |
| 4496 | Integra LifeSciences Boston, MA ENGINEER II, QUALITY Master degree in Quality Assurance, Biological Sciences or discipline. Exp: 0-2 years |
The Quality Engineering team focuses on product compliance in support of Product Design and Manufacturing, including the critical quality system elements of CAPA, Complaint Investigations, Risk Management, Process/Test Method/Equipment Validations, Deviations, Control of Nonconforming Product, Product Holds, Microbiology and Equipment management. Works closely with Operations, Manufacturing Engineering, Design Engineering and Post-Market Surveillance groups to ensure a high level of product quality and effective and efficient investigations when needed. | 6/29/2023 |
| 4497 | Integra LifeSciences Boston, MA ENGINEER II, QUALITY VALIDATION Master degree in Engineering (Biomedical, mechanical, chemical, or electrical) or Science (Biology, Chemistry) Exp: 0-2 years |
Responsibilities associated with this position are directly associated with the introduction and launching of new or products and processes into a manufacturing facility. The candidate must utilize problem solving techniques to resolve issues and conflict in order to meet the high level goals set forth by the organization. The candidate must be well organized and technically sound in understanding scientific rationale and justifying criterion from a quantitative standpoint. The candidate must be familiar with process flow of a medical device organization, including the regulatory impact of change and the documentation path of a compliant process. The candidate must possess technical writing experience in protocol generation and procedure generation. Some experience is required in master plan generation and the change control life cycle. The candidate must be a team player who thrives in a team environment, but also has the capability to work on their own to research and investigate. Gown qualification is a plus, with an understanding of clean room practice and cGMP environments. The qualified candidate must understand the concepts of risk management and the ability to identify and classify critical parameters within a production setting. | 6/29/2023 |
| 4498 | IQVIA Austin, TX Laboratory Associate - Automation Bachelor’s Degree in Chemistry or a related field. Exp: 1 year |
Responsible for routine sample preparation duties inclusive of automated liquid handling, troubleshooting routine experiments and the preparation of solutions. | 6/29/2023 |
| 4499 | IQVIA Santa Fe, NM Research Associate Bachelor’s degree or higher in Biology, Biochemistry, Molecular Biology, or related life science fields Exp: 1+ years |
You will assist our scientific team in empowering Pharma companies to develop new antibody-based therapeutics. We expect you to be enthusiastic, curious, and to have a strong team player attitude. You will be hired as part of the Laboratory Operations Team, which provides support to the entire Specifica Scientific Team. | 6/29/2023 |
| 4500 | IQVIA Durham, NC Scientist, Assay Development Bachelor's Degree in relevant scientific discipline (Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technol Exp: 1 year |
The Scientist for Assay Development contributes to the design of and is responsible for experiment execution of assay/method development. | 6/29/2023 |
| 4501 | IQVIA Ithaca, NY Associate Scientist,Sample Prep (Sign on bonus offered) Bachelor's Degree in a Life Sciences discipline required. Exp: 6 months |
Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments and the preparation of solutions and reagents. | 6/29/2023 |
| 4502 | IQVIA Valencia, CA Laboratory Associate- Microbiology Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree required. Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 6/29/2023 |
| 4503 | IQVIA Valencia, CA Laboratory Associate- Automated Chemistry Bachelor's Degree. Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree required. Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 6/29/2023 |
| 4504 | IQVIA Atlanta, GA Laboratory Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required. Exp: 6 months |
Shift Tuesday-Saturday 3:00PM-11:00PM Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 6/29/2023 |
| 4505 | MEDTOX Greenfield, IN Research Assistant BS/BA degree in science or related field. Exp: 1+ years |
Performs basic laboratory operations independently with detailed review of results by experienced personnel Incumbent has a basic understanding of the technical area of responsibility. | 6/29/2023 |
| 4506 | MEDTOX Somerset, NJ Research Analyst - BioAnalytics Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Research Analyst on our BioAnalytical team in Somerset, NJ. Are you interested in working in the research field? Do you have LCMS experience? Join an organization that truly believes in employees learning and growing a career. The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time between 6am and 9am. | 6/29/2023 |
| 4507 | MEDTOX Raritan, NJ Technologist Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Technologist or Technician in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Esoteric Dept. The work schedule for this position will be Mon-Fri 11:30PM - 8:00AM, Rotating weekends | 6/29/2023 |
| 4508 | MEDTOX Raritan, NJ Cytotechnologist Bachelor of Science degree from an accredited college/university. Successful competition of an accredited Cytology program. ASCP Cytotechnologist (CT) Exp: 1 year |
This position includes a $15,000 Sign-On Bonus! (External candidates only) Are you a certified Cytotechnologist? Are you in school pursuing a Cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time Cytotechnologist in Raritan, NJ. This will be a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives. Schedule: Monday through Friday between the hours of 6:00am and 7:00pm, and every 3rd Saturday | 6/29/2023 |
| 4509 | MEDTOX Raritan, NJ Clinical Laboratory Technologist- Hematology Department Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Technologist or Technician in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Monday- Friday, 11:30 PM- 8:00 AM, Alternating Saturday | 6/29/2023 |
| 4510 | MEDTOX Raritan, NJ Clinical Laboratory Technologist - Immunology Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be 2.00pm to 10.30pm ; Tuesday to Saturday | 6/29/2023 |
| 4511 | MEDTOX Raritan, NJ Clinical Laboratory Technologist - Mass Spectrometry Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Technologist or Technician in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Tuesday- Saturday, 10:00pm - 6:30am. | 6/29/2023 |
| 4512 | Merck Durham, NC Associate Manufacturing Automation Specialist B.S., B.A., or greater preferably in Engineering, Science, or Information Technology Exp: 1+ years |
The Associate Manufacturing Automation Specialist position shall support the expansion of a GMP testing laboratory at a manufacturing facility for sterile vaccine products. Responsibilities include supporting computer system validation, implementing process control and data collection, and troubleshooting in compliance with SDLC, cGMP, safety, and environmental regulations. The Manufacturing Automation Associate Specialist must actively support, participate, and embrace an empowered team culture including significant interaction with manufacturing, quality, IT, and engineering groups. This role supports a large spectrum of sophisticated automated systems within Laboratory Operations; providing multiple opportunities to learn new automation technologies and make a positive impact. | 6/29/2023 |
| 4513 | Merck West Point, PA Engineering, Maintenance & Utilities 2nd Shift Associate Specialist B.S. Engineering, Science, or four-year Engineering Technology Degree Exp: 1+ years |
Under the supervision of a Senior Specialist or Associate Director, the EMU Associate Specialist is responsible to provide day-to-day equipment and facility engineering support for assigned area including vaccine bulk manufacturing, and/or associated facility/utilities mechanical support. Assigned tasks include support and monitoring of equipment performance and maintenance, propose and develop equipment and facility improvements and troubleshoot process equipment to ensure reliable, compliant and efficient operations. Actively ensures compliance to current Good Manufacturing Practices (GMP), Safety, and Environmental regulations while achieving operating cost goals. | 6/29/2023 |
| 4514 | Merck Rahway, NJ Scientist, Small Molecule Analytical Research & Development Master of Science degree in Chemistry, Pharmaceutical Sciences, or related fields. Exp: 0 years |
The Small Molecule Analytical Research and Development group has an opening for a Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Scientist, you will be part of a team of Analytical Chemists working on cross-functional scientific teams to enable novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization and statistical data analysis. | 6/29/2023 |
| 4515 | Merck Rahway, NJ Process and Data Engineer Bachelors or higher in Mathematics, Statistics, Economics, Business Information Systems, Computer Science/MIS, Finance/Accounting, Engineering, Scienc Exp: 1-4 years |
Our Quantitative Sciences team use big data to analyze the safety and efficacy claims of our potential medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality data to support decision making in clinical trials. | 6/30/2023 |
| 4516 | Merck Kenilworth & Rahway, NJ Associate Scientist, Sterile & Specialty Products. This Job Is Available In 2 Locations. B.S. degree in Chemical / Biochemical / Biomedical Engineering, Materials Science, Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Sciences, C Exp: 1+ years |
We are seeking a motivated engineer / scientist to work collaboratively in a team environment to help solve key challenges in formulation development and manufacturing of parenteral pharmaceutical products. The successful candidate will be a passionate scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible for supporting the formulation development of new biological / chemical entities as part of a matrix team from initial first-in-human formulations to commercialization. The successful candidate must be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. | 6/30/2023 |
| 4517 | Merck West Point, PA Shift Engineer - 3rd Shift, Monday - Friday BS in Engineering or comparable scientific background. Exp: 1 years |
Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. Position Description: The function of this position is to provide technical support for vaccine purification facility while actively supporting, participating in, and embracing an empowered culture. This role is for Off-Shift Engineering Support (3rd Shift, Monday through Friday). 3rd shift (12am-9am) | 6/30/2023 |
| 4518 | Stryker Portage, MI Electrical Design Engineer(ENTRY LEVEL) Bachelor's degree in EE or related discipline. Exp: 0-2+ years |
We are currently looking for an Electrical Design Engineer to be responsible for a wide variety of engineering work in support of current production medical devices including design changes, process/quality improvements and compliance issues. You will also support and conduct root cause analysis, verification and validation testing, manufacturing transfer activities and component obsolescence management for existing products. | 6/20/2023 |
| 4519 | Stryker Salt Lake City, UT Manufacturing Engineer Bachelor’s degree in Engineering required. Exp: 1+ years |
Stryker’s Neurovascular Manufacturing division is seeking to hire a Manufacturing Engineer in Salt Lake City, Utah. | 6/20/2023 |
| 4520 | Stryker Portage, MI Mechanical Engineer, R&D – Sustainment Bachelor’s Degree in Mechanical Engineering Exp: 0+ years |
Stryker is seeking to hire a Mechanical Engineer, R&D to support Medical’s Acute Care Product Engineering team. This role is hybrid, in Portage, MI with the expectation to come into the office a minimum of 3 days a week. | 6/20/2023 |
| 4521 | Acrotech Biopharma East Windsor, NJ CHEMIST A BS/MS in a Scientific field. Exp: 1-3 years’ |
The Chemist will perform a variety of testing to assess the strength, identity and purity of finished product, which are mainly oral solids and/or raw materials. The Chemist will work as a member of a team to effectively plan and develop/validate new methods (for Assay, Dissolution, Residual solvents, and Related compounds tests) to execute analytical testing and/or test using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 6/20/2023 |
| 4522 | Acrotech Biopharma East Windsor, NJ ASSOCIATE, AUTOMATION ENGINEER Masters in Industrial & Systems Engineering or Mechanical Engineering Exp: 1-2 Years |
The role of the Automation Engineer is to perform as-is study of current process and provide recommendation on Automating and de-skilling current manual process. Associate should be willing to learn and work on ERP, Warehouse Control System, PLC , HMI and has logical approach towards trouble shooting a problem The position works closely with Automation & Project Management team, on the new requirements and enhancements and takes up continuous improvement projects to drive the operational efficiencies across the Distribution Center | 6/20/2023 |
| 4523 | Meridian Bioscience Memphis, TN Lab Production Associate Bachelor’s or Master’s degree from an accredited institution with a relevant scientific discipline such as Chemistry, Biology, Biochemistry, Molecular Exp: 1+ years |
The Lab Production Associate position is responsible for performing assigned manufacturing and laboratory support activities according to company policies, SOPs, and quality regulations. The position will be responsible for performing upstream and downstream bioprocessing procedures to support the commercial manufacturing of native antigens, recombinant proteins, antibodies, and blockers. Upstream processes include tissue culture, cell bioreactors, fermentation, virus propagation, cell and virus bank production, and buffer/media preparation. Downstream unit operations include harvest, clarification, chromatography, centrifugation, TFF (UF/DF), filtration, formulation, and fill-finish. The candidate will be required to maintain an assigned lab area and perform equipment and lab cleaning procedures. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO1345 regulations. | 6/20/2023 |
| 4524 | Repligen Waltham, MA ELISA Manufacturing Associate I - 2nd shift AS/BS in biotechnoloy related study. Exp: 0-2 years |
This position will function in Repligen’s ELISA group. The successful candidate will play a key role in ensuring that the ELISA department's production and quality goals are met. The individual must be able to follow oral and written instructions accurately and complete tasks in a timely manner. Experience working in a GMP/ISO/document-controlled environment would be beneficial. Attention to detail and the ability to work independently and in a team environment are essential. Candidates must be willing and able to learn new manufacturing processes as the company grows. This position will support the 2nd shift. | 6/20/2023 |
| 4525 | Cosette Pharmaceuticals South Plainfield, NJ Research Scientist I Master’s degree in chemistry or pharmacy. Exp: 1-2 years |
The Research Scientist I will be responsible for: • Analytical method Development and Validation • Development and Validation of In vitro methods for Complex generic dosage forms • Maintain full compliance with US FDA – cGMP regulations. • Resolve technical problems and participate in troubleshooting when required | 6/22/2023 |
| 4526 | Delfi Diagnostics Palo Alto, CA Clinical Laboratory Associate, Contractor (Tues-Sat) BS in Biomedical Laboratory Sciences, Clinical Science, or equivalent. Exp: 1+ years |
In this role, you will be responsible for the pre-analytical phase of testing (e.g., specimen receipt, accessioning, and plasma/buffy coat isolation) and assisting with general laboratory operations, such as equipment maintenance, labware cleaning, and reagent manufacturing. | 6/22/2023 |
| 4527 | DiabetOmics Hillsboro, OR Research Assistant/Associate in Product Development (2 positions available immediately) BA/BS in a relevant biological science. Exp: 1-2 years |
Applies knowledge of scientific principles and concepts to the design, development, and execution of Product Development experiments. Demonstrates technical proficiency, scientific creativity, collaboration with others and can work independently. Under guidance of senior personnel, designs and conducts research and/or product development, assay optimization and scale-up tasks and experiments based on the needs of the group. Ensures compliance with and helps to implement the requirements of working in a regulated environment to assure adherence to various requirements, including Design Control, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP). Helps to coordinate general laboratory tasks such as reagent preparation, inventory and organization of work. | 6/22/2023 |
| 4528 | Dicerna Pharmaceuticals Lexington, MA Research Associate - Chemistry Bachelors or Masters in Chemistry or related field. Exp: 1-3 years |
Dicerna Pharmaceuticals is seeking a highly motivated Research Associate with a strong background in synthetic and medicinal chemistry to join the Chemistry Team. The candidate will be responsible for the synthesis of oligonucleotide conjugates, nucleoside analogues, small molecule ligands, and linkers. This position will contribute to the development of novel nucleic acid conjugate platforms and support therapeutic programs in multiple disease areas. The Dicerna research team will provide an exciting learning opportunity and a collaborative and fast-paced research environment. | 6/22/2023 |
| 4529 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 6/22/2023 |
| 4530 | DxTerity Rancho Dominguez, CA Research Associate B.S. or M.S Degree in Biochemistry, Molecular Biology or a related field. Exp: 1-3 years |
DxTerity, a patient-centric genomics company located in Los Angeles, CA is looking to hire a Research Associate to join our Research and Product Development team. Responsibilities include: development of molecular diagnostic test kits, reagents and procedures in a team environment. Perform experiments independently after receiving general direction from supervisor. Make detailed observations, analyzes data and interpret results. Prepare technical reports, summaries, protocols and quantitative analyses. Maintain and develop skills in molecular biology and company technology through reading of internal reports and scientific literature. Support the achievement of project objectives and time schedules while meeting ISO and FDA regulatory and design control requirements. | 6/22/2023 |
| 4531 | Ensoma Boston, MA Associate Scientist, Genomics Master’s Degree in a biological science. Exp: one year |
We are seeking an energetic and highly motivated Associate Scientist to join our Platform team. In this role, you will execute standard molecular biology workflows and work collaboratively between groups across the company andperform various next generation sequencing (NGS) assays to characterize and assess therapeutic efficacy and safety. You will partner with top-notch scientists and have an opportunity for accelerated technical skill development and diverse growth and learning opportunities. Do you have a passion for pioneering therapeutics technology development utilizing a broad spectrum of gene editing and modification tools? Are you a great team player, enthusiastic and do you enjoy working in an innovative, collaborative, and fast-paced environment? Join us and be part of a company moving novel gene therapies into the clinic, revolutionizing the reach and access of the curative power of genomic medicines for patients with serious diseases. | 6/22/2023 |
| 4532 | Exagen Diagnostics Vista, CA Laboratory Technician Bachelor’s degree or college courses in Science. Exp: 1+ years |
Responsible for general laboratory task such as buffer preparation and operation of appropriate laboratory equipment. Take direction from and works in collaboration with Technologist in Flow cytometry department. | 6/22/2023 |
| 4533 | Flexion Therapeutics San Diego, CA QA Associate 1 BS/BA degree in scientific discipline from an accredited college or university. Exp: 1 year |
This person is to assist and support the organization with GMP compliance, monitoring conformance to established quality assurance processes and GMP standards for manufacturing. | 6/22/2023 |
| 4534 | Fluxergy Irvine, CA Process Engineer Engineering Degree Exp: 0-2 Years |
As the process engineer at Fluxergy, you will be directly involved in the company’s production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process ownership while working with a small but passionate team. This position requires a deep, in-depth knowledge of manufacturing processes, stability and process control. | 6/23/2023 |
| 4535 | Foghorn Therapeutics Cambridge, MA Research Associate - Biochemistry & Biophysics BA/BS in Biochemistry, Biophysics, or related field. Exp: 1+ year |
Foghorn is seeking a highly motivated, enthusiastic, and collaborative Research Associate to join our Drug Discovery team in a lab-based role to support early discovery projects in oncology. As a member of our Drug Discovery team the candidate will have an opportunity to employ various biochemical and biophysical assay technologies in mechanism of action studies, screening and hit validation. This is an onsite and lab based role. | 6/23/2023 |
| 4536 | Frontida BioPharm Vandalia, OH QA Technician I or II (2nd Shift) Bachelor’s Degree required preferably in a related field (i.e., pharmaceutical sciences, chemistry, biology). Exp: 0 - 5 years' |
The QA Technician is responsible for providing quality support to the manufacturing floor, auditing batch production documentation, dispositioning intermediates, performing in process checks, identifying and logging incident reports, and ensuring adherence to cGMP. | 6/23/2023 |
| 4537 | Frontida BioPharm Vandalia, OH QC Chemist I (3rd Shift) Bachelor’s degree in Chemistry or closely related field. Exp: 0-2 years' |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 6/23/2023 |
| 4538 | Frontida BioPharm Vandalia, OH Formulation Technician Bachelor’s Degree in a scientific or engineering discipline preferred. Exp: 1+ years’ |
The Formulation Technician will report to the Associate Director of Formulations and will assist the R&D Formulations staff with product development activities from small scale to commercial batch production. The Formulation Technician should be someone with a keen interest in life sciences or drug manufacturing. This is a developmental role where training is provided, offering an opportunity to learn various techniques of drug manufacturing including dispensing, blending, granulation, compression and coating. | 6/23/2023 |
| 4539 | Fujifilm Diosynth College Station, TX Manufacturing - Associate Process Engineer Bachelor’s degree in Science, Engineering, or other related field. Exp: 1 year |
The Manufacturing Associate Process Engineer is an integral part of the Manufacturing Technical Operations department in College Station, Texas. This position will report directly to the Manager of Technical Operations. Works independently and with colleagues to provide expertise and assistance for the design, development, standardization, and maintenance of an operational biotechnology utilized to manufacture various proteins and other drug substances. This person would provide manufacturing technical support on core manufacturing and operational technologies for the manufacturing unit. Operational biotechnologies include 1. USP: Isolators and biosafety cabinets and their use in cell propagation, Cell Culture/Single Use Technology for adherent and suspension culture; 2. DSP: Dispensing and Mixing and Buffer Preparation, Chromatography, Tangential Flow Filtration, various filtration technologies, centrifugation, and Bulk Fill. This position will also create training programs and perform training for manufacturing technicians in the unit operation categories. | 6/23/2023 |
| 4540 | Fujifilm Diosynth College Station, TX Process Sciences - Associate Engineer Bachelor’s Degree Exp: 1 years |
The Process Sciences - Associate Scientist/Engineer, under general direction, functions within a team based organization to actively address cGMP manufacturing issues. The individual is responsible for analyzing process technologies to assist in the technical transfer of new processes into the manufacturing group. This individual must work in a collaborative manner to assist the transfer of biological drug processes from process development (internal or client) groups in a CDMO environment. | 6/23/2023 |
| 4541 | Fujifilm Diosynth College Station, TX Quality Control - Microbiology Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field. Exp: 0+ years |
The Microbiology Analyst I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. | 6/23/2023 |
| 4542 | Fujifilm Diosynth College Station, TX QA Analyst I Bachelor’s degree in a related science concentration. Exp: 1+ years |
The Quality Assurance (QA) Analyst I, under direct supervision, will be responsible for assisting with the review and/or approval of basic and technical documentation; Drafting and reviewing of internal Quality policies and procedures; Assisting with product related activities; Assisting with Quality audit functions; Identifying process and Quality System improvements; | 6/23/2023 |
| 4543 | Fujifilm Diosynth Holly Springs, NC Manufacturing Associate II/III *Multiple Positions* MA III: BA/BS Degree in Life Sciences or Engineering. Exp: 0+ years |
The Drug Substance Manufacturing Associate during the project phase is responsible for activities associated with factory acceptance testing (FAT), commissioning, qualification, and validation (CQV) of drug substance process equipment. During the project phase, and as CQV activities allow, create and/or review of manufacturing work instruction or procedures or other manufacturing operational readiness tasks will be required. Travel will be required. At project completion, the associate would transition into manufacturing operations as a manufacturing associate in Drug Substance Manufacturing (DSM) Cell Culture or Purification areas requiring shift work (nights and weekends). | 6/23/2023 |
| 4544 | Fujifilm Diosynth College Station, TX Manufacturing Technician III Bachelor’s degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or other related field. Exp: one (1) year |
The Manufacturing Technician III will work directly with a range of technologies. Dependent upon assignment. | 6/23/2023 |
| 4545 | GenMark Diagnostics Seattle, WA Laboratory Assistant I Bachelor’s degree focused in Biology, Biotechnology, Biochemistry, Chemistry, Physics or Engineering field preferred. Exp: 1+ years |
We are seeking driven, self-motivated, and passionate individuals looking to start a career in a fast-paced lab. The position will play an integral role in day-to-day operations as we develop our novel DNA sequencing technology. This position will be based at Roche Diagnostics Seattle, formerly Stratos Genomics. A cover letter is required to be considered for this role. In the cover letter, please be sure to explain how you will meet the below requirements as well as address the following: the technology that Roche Diagnostics Seattle (formerly Stratos Genomics) is developing, why you want to work here, and how you would contribute. | 6/23/2023 |
| 4546 | GenMark Diagnostics Seattle, WA Laboratory Assistant I Bachelor’s degree focused in Biology, Biotechnology, Biochemistry, Chemistry, Physics or Engineering field preferred. Exp: 1+ years |
We are seeking driven, self-motivated, and passionate individuals looking to start a career in a fast-paced lab. The position will play an integral role in day-to-day operations as we develop our novel DNA sequencing technology. This position will be based at Roche Diagnostics Seattle, formerly Stratos Genomics. A cover letter is required to be considered for this role. In the cover letter, please be sure to explain how you will meet the below requirements as well as address the following: the technology that Roche Diagnostics Seattle (formerly Stratos Genomics) is developing, why you want to work here, and how you would contribute. | 6/23/2023 |
| 4547 | GenMark Diagnostics Seattle, WA Lab Assistant II - SBX Nanopore Technology Bachelor’s degree in Molecular biology, Protein Engineering, Bioengineering, Biochemistry or related field. Exp: 1 year |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its novel Sequencing by eXpansion (SBX™) technology. SBX™ uses unique applications from chemistry, biochemistry, electrochemistry, and protein engineering to sequence DNA by nanopore in rapid time with high accuracy and low cost. The Sequencing team is devoted to developing our high throughput, low-cost DNA sequencing approach into an industry disrupting product that will facilitate the care that patients need. | 6/23/2023 |
| 4548 | Gritstone Oncology Pleasanton, CA RESEARCH ASSOCIATE I, PROCESS DEVELOPMENT (CONTRACT) Bachelor’s degree (or equivalent) in a scientific discipline or a health-related field. Exp: 0 to 2+ years |
We are looking for an enthusiastic and flexible team player who will thrive in a fast-paced, dynamic, and highly collaborative environment. This individual will work in Process Development Group and contribute to the development of novel adenovirus vaccines and their transfer to manufacturing. | 6/23/2023 |
| 4549 | Haemonetics Boston, MA Reagent Chemist In-Vitro Diagnostics MS in a relevant discipline such as Chemistry, Biochemistry, Biology, Biomedical Engineering, Chemical Engineering, or equivalent. Exp: 0+ years |
Reagent Chemist In-vitro Diagnostics Research & Development Hemostasis Management Hospital Division Boston, MA The Reagent Chemist works alongside a multidisciplinary development project team, responsible for ensuring that the in-vitro diagnostic system, under development, meets its intended goals. The person in this role will develop, optimize and validate reagents for an in-vitro diagnostic system. This role will have technical responsibility for performing testing of raw materials and in-process reagents to support development and transfer to the manufacturing process. | 6/23/2023 |
| 4550 | HistoTox Labs Rockville, MD Laboratory Technician I A Bachelor’s degree in a scientific discipline (i.e., biological sciences, Chemistry, etc.). Exp: 0+ years |
Seeking a Laboratory Technician for our Rockville, MD site. | 6/23/2023 |
| 4551 | HistoTox Labs Rockville, MD Associate Scientist Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.). Exp: 1+ years |
Seeking an Associate Scientist I (In Vitro Cytogenetics). | 6/23/2023 |
| 4552 | HistoTox Labs Madison, WI Upstream Biomanufacturing Laboratory Support Technician Bachelor of Biological Sciences a plus. Exp: 1+ years |
The Laboratory Technician, Upstream Biomanufacturing and Quality Control Testing, will be a member of the lab service’s in vitro biomanufacturing team. The position involves culturing, customer provided, hybridoma cells that produce monoclonal antibodies. Once produced the antibodies are refined, quality control tested, and the finished product is delivered. The company is well established and growing, with a worldwide customer base. Your exciting new career will be cultivated in an environment of continuous improvement. | 6/23/2023 |
| 4553 | Ifyber Ithaca, NY Laboratory Technician BS degree Exp: 1 year + |
The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. | 6/23/2023 |
| 4554 | IGM Biosciences Mountain View, CA Research Associate I / II, Downstream Process Development BS degree in chemical / biochemical engineering, biochemistry, or related field. Exp: RA I: BS with 0+ years; RA II: MS with 0+ years. |
As a Research Associate with experience in process development particularly in the context of antibody and antibody-like biologics. The ideal candidate will have a solid background in protein purification and bioanalytical techniques used to characterize biologics. This is a key position in Process Development and Manufacturing and will have the opportunity to collaborate across groups to contribute to multiple fast-moving drug discovery projects. You will report to a Senior Scientist. | 6/23/2023 |
| 4555 | Imperative Care Campbell, CA Process Development Engineer Bachelor/Master’s in Engineering or related discipline. Exp: less than 2 years |
The Process Development (PD) Engineer I will learn about and assist in product development projects defining, characterizing, optimizing, and validating stable, robust, and capable processes for neuro-interventional medical devices. They will assist in the improvement of internal equipment and processes. Responsibilities will include creative problem solving, critical thinking, application of engineering principles performing process characterization studies, collecting, and analyzing data, and documenting equipment/processes. | 6/23/2023 |
| 4556 | Imperative Care Campbell, CA Preclinical R&D Engineer, II Bachelor's degree in Engineering: mechanical, biomedical, or related discipline, or a Master's degree. Exp: BS: 1+ years ; MS: 0+ years |
What You’ll Do – in this role as a Preclinical R&D Engineer, II, you will have the unique opportunity to work in a small, dynamic team environment advancing the standard of care for stroke treatment through preclinical research and development, anatomical modeling and physician evaluations while working with new product development and commercial teams. This role will be responsible for designing and managing all aspects of physician evaluations, in-vitro bench and simulated use testing, and in-vivo studies, and will partner with Marketing representatives to create marketing collateral via bench and in-vitro testing. | 6/23/2023 |
| 4557 | InBios International Seattle, WA Manufacturing Associate I- ELISA Bachelor’s degree with emphasis on life science. Exp: 1-year |
We are searching for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other InBios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale ELISA diagnostic test components in a BSL-2 laboratory. If you are seeking an entry-level, full-time, on-site position where you can gain experience and grow at the forefront of medical diagnostic biotechnology, this is a great opportunity for you. | 6/23/2023 |
| 4558 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required. Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 6/13/2023 |
| 4559 | Cabaletta Bio Philadelphia, PA Research Associate/Sr. Research Associate, Molecular Biology B.S degree in Life Sciences/Engineering or closely related discipline. Exp: 1-3 years |
Reporting to the Scientist, Molecular Biology we are seeking an experienced, motivated detail-oriented, and highly skilled Research Associate/ Sr. Research Associate within our Molecular Biology Team. Under scientific and technical supervision, the individual will primarily be responsible for manufacturing small and large scale LVV gene therapy vectors across various preclinical programs and disease areas. The candidate should be a highly motivated self-starter with well-established organizational skills who is excited to be a part of the biotechnology industry. The position offers potential growth into additional areas such as molecular biology, immunology, and cell therapy. | 6/14/2023 |
| 4560 | Cabaletta Bio Philadelphia, PA Research Associate/Senior Research Associate, Analytical Development Bachelor’s or master’s degree in biology or closely related discipline. Exp: 1-3 years |
Reporting to the Senior Scientist, Analytical Development, this experienced and motivated Research Associate / Senior Research Associate will support activities of routine analytical testing and method development/qualification to advance CARTA and CAART platforms for pre-clinical and clinical programs. | 6/14/2023 |
| 4561 | Capricor Therapeutics Los Angeles, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences or related field. Exp: 1-3 years |
This position is immediately available to join our Manufacturing team to perform cGMP manufacturing to support Capricor’s clinical trials and exosome development. We are seeking an individual with a scientific background, mammalian cell culture and cGMP experience. | 6/14/2023 |
| 4562 | Capricor Therapeutics San Diego, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences or related field. Exp: 1-3 years |
This position is immediately available to join our Manufacturing team to perform cGMP manufacturing to support Capricor’s clinical trials and exosome development. We are seeking an individual with a scientific background, mammalian cell culture and cGMP experience. | 6/14/2023 |
| 4563 | Abiomed Danvers, MA Equipment Design Engineer I Bachelor’s degree in a Engineering, such as Mechanical Engineering, Industrial Engineering, or Mechanical Design. Exp: 1+ years |
The Equipment Design Engineer I will support , design, develop, and improve, tooling and fixtures for new and existing production floor equipment. In this role, you will be required to meet with different teams to determine their design requirements, plan and execute the design of tools/equipment , develop and test prototypes, and work closely with the manufacturing teams to ensure that design specifications are met. This also includes supporting your peers in design and drafting, engineering change control and equipment qualification, validation, and installation activities. This role will also assist in designing and developing equipment with counterparts in our Aachen, Germany facility. | 6/15/2023 |
| 4564 | Abiomed Danvers, MA Supplier Development Engineer I Bachelor's Degree in Engineering, preferably in Mechanical, Plastics or Manufacturing Engineering Exp: 1+ years |
The Supplier Development Engineer I serves as ABIOMED’s primary technical contact with all US based suppliers, leads all product development team’s supplier initiatives, second source critical suppliers, and establishes “Quality at the Source” programs with key partners. This role is a key technical resource for the company’s continued growth, and is a great opportunity for someone to make a difference at one of the fastest-growing medical technology companies, focused on recovering hearts and saving lives. | 6/15/2023 |
| 4565 | Agilent Boulder, CO Research Associate, Analytical Services Bachelor's degree (B. S.) or equivalent in chemistry, related applied sciences field. Exp: 1+ years |
As a Research Associate in the Analytical Services team the candidate will be responsible for performing sample analysis and supporting analytical method validation. | 6/15/2023 |
| 4566 | Amgen Thousand Oaks, CA Associate - Protein Chemistry Bachelor’s degree in Biochemistry, Biophysics, Analytical Chemistry or related field. Exp: 1+ years |
Let’s do this. Let’s change the world. We are seeking a skilled biochemist to join the Protein Chemistry group within the Protein Engineering Division of Therapeutic Discovery. The Protein Chemistry group is primarily responsible for the optimization, production, assessment, and selection of novel and complex scaffold molecules, often antibody-based, that will be the next generation of large molecules therapeutics. In this vital role you will be a part of a multidisciplinary team with capabilities in protein purification and characterization of large molecule drug candidates. You should be able to interpret and report scientific results that support the generation of publications, patents, or regulatory submissions, and participate in internal and external scientific meetings. Good written and oral presentation skills are a must | 6/15/2023 |
| 4567 | AstraZeneca Gaithersburg, MD 80109216 Associate Scientist - Purification Process Sciences Bachelor's or Master's Degree in Biochemistry, Chemical Engineering, or related field. Exp: 0+ years |
In this role, the Associate Scientist will need to develop and characterize downstream processes for the manufacture of biopharmaceuticals (monoclonal antibodies and other proteins) in late stage clinical development through commercial launch. He / She will be responsible for a portion of a purification development project which will require the scientist to make observations, analyze data and interpret results. | 6/15/2023 |
| 4568 | Bristol-Myers Squibb Redwood City, CA Associate Scientist, In Vivo Pharmacology, Tumor Microenvironment Research Master’s Exp: 0-3+ years |
You will design, plan, and execute in vivo studies, analyze, and present data. You will gain and provide technical and scientific in vivo pharmacology expertise to advance drug discovery programs from target identification/validation to IND enabling activities. You will interact and collaborate effectively in a multi-functional dynamic team environment. | 6/15/2023 |
| 4569 | Bristol-Myers Squibb Devens, MA Associate Scientist/Engineer, MS&T MS in Chemical/Biochemical Engineering or related field. Exp: 0–4 years |
The Associate Scientist, Downstream position in Manufacturing Technology supports the commercial manufacturing of biopharmaceuticals in purification and primary recovery. This position offers the opportunity to provide highly visible technical leadership to resolve complex problems while meeting quality, schedule, and cost objectives. The successful candidate will be a key contributor in a dynamic and highly collaborative team environment. The candidate will set appropriate objectives and priorities, overcome obstacles; and deliver results within project timelines. Expertise and experience in the design, control, and operation of protein purification steps like - chromatography steps, ultrafiltration and diafiltration, micro- and nano- filtration unit operations are highly desired. Demonstrated skills in cross-functional partnerships, supporting cross-functional teams and knowledge of regulatory and cGMP requirements are required. | 6/16/2023 |
| 4570 | Bristol-Myers Squibb Devens, MA Production Engineer/Scientist 1 Bachelor’s degree in Engineering (Chemical, Mechanical, Industrial, Biomedical Engineering) or Life Sciences (Chemistry, Biochemistry, Microbiology) Exp: 0+ years’ |
Reporting to the Shift Manager, Production Engineer/Scientist 1 of the Single Use Facility is responsible for advancing the biologics pipeline according to established work instructions and in accordance with current Good Manufacturing Practices (cGMPs). The role is based in a state of the art facility utilizing single-use technology. The Production Engineer/Scientist 1 is responsible for mastering all routine manufacturing assignments/processes, providing daily technical oversight of execution of manufacturing processes, provide in depth training, maintaining a culture of compliance, and innovation within the downstream team. The Production Engineer/Scientist 1 is required to guide the shift personnel with technical knowledge to lead troubleshooting activities, provide investigation support, analyze process/equipment data, and identify and implement process improvements. | 6/16/2023 |
| 4571 | Bristol-Myers Squibb Warren, NJ Assistant Scientist, Clinical Quality Control- Cell Therapy Bachelor’s degree required, preferably in chemistry, microbiology, or related science. Exp: 0-3 years |
The Assistant Scientist, Clinical QC Sample Management position is responsible for the movement and control of Quality Control (QC) samples and materials in support of the QC laboratories at the CAR T manufacturing facility in Warren, NJ. This primarily includes, but is not limited to, sample collection and distribution, inventory control, chain of custody, sample tracking, documentation, and shipments within the cGMP operation for CTDO Developmental QC for CAR T. | 6/16/2023 |
| 4572 | Covance Greenfield, IN Research Assistant BS/BA degree in science or related field. Exp: 1+ years |
Performs basic laboratory operations independently with detailed review of results by experienced personnel Incumbent has a basic understanding of the technical area of responsibility. | 6/16/2023 |
| 4573 | Covance Herndon, VA Cytotechnologist Bachelors of Science degree in Biology, Chemistry, Medical Technology or Related Life Science. Successful competition of an accredited Cytology progra Exp: New grads welcome! |
$10,000 Sign-On Bonus for External Candidates Only! Are you a certified Cytotechnologist professional, looking for an exciting and challenging change? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time Cytotechnologist in Herndon, VA! This will be a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives. The work schedule for this position will be: 1st shift, Monday - Friday, 8:00am-4:30pm (ability for flexible start times between 6:00am-9:00am). | 6/16/2023 |
| 4574 | Covance Fort Washington, MD Histotechnician Associate's or Bachelor's Degree in a Life Science and meet local regulatory (CLIA & State) requirements. Histology and/or ASCP certifications are pre Exp: 0+ years |
Process human tissue and body fluid specimens in preparation for microscopic exam Perform technical duties related to the production of histopathological slides of surgical specimens Section the embedded tissue, using a microtome and mount the section properly on a microscope slide Perform various immunohistochemical tests on formalin fixed paraffin embedded tissue sections Process mounted sections through routine and special staining procedures Properly orient and embed surgical tissue specimens Prepare the stains and reagents needed for special procedures Report accurate and timely test results in order to deliver quality patient care | 6/16/2023 |
| 4575 | Covance Baltimore, MD Clinical Laboratory Technologist Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1+ years |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist/Clinical Lab Technician in Baltimore, MD. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Schedule: 3rd Shift; Mon - Fri (11:30p - 7am); rotating weekends | 6/16/2023 |
| 4576 | Covance Richmond, VA Medical Lab Technologist Exp: |
$2,000 SIGN ON BONUS Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Laboratory Technician OR Technologist in Richmond, VA. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". The schedule for this position is Monday - Friday 7:30a-5:30p, with various start times. This position is a Float opportunity. You will be covering 6 different sites. As a Float Technician, you will be partially reimbursed for your Mileage and receive additional compensation. | 6/16/2023 |
| 4577 | Covance Raritan, NJ Technologist Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1+ years |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Technologist or Technician in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Sun - Thurs - 8:00AM - 4:30PM - With rotating holidays Esoteric/Serology department | 6/16/2023 |
| 4578 | Covance Raritan, NJ Clinical Laboratory Technologist - Immunology Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Thursday to Sunday (10.00pm to 8.00am rotating weekend as needed ) | 6/16/2023 |
| 4579 | Exact Sciences San Diego, CA Research Associate II Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day to day experimentation and is responsible for the execution of bench experiments and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 6/16/2023 |
| 4580 | Exact Sciences San Diego, CA Research Associate II Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day to day experimentation and is responsible for the execution of bench experiments and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 6/16/2023 |
| 4581 | Leidos Biomedical Research Groton, CT Chemistry Technician Bachelor's degree in Chemistry or related fields. Exp: 0-2+ years |
Recognized as a Top 10 Health IT provider, the Leidos Health Group draws on decades of success to deliver a range of solutions and services designed to meet the healthcare challenges of today. From the research bench to the patient bedside, we are a company of scientists, engineers, and technologists delivering a broad range of impactful, customizable, and scalable solutions to hospitals and health systems, biomedical organizations, and every U.S. federal agency focused on health. Leidos works with customers across the continuum of care to improve clinical, operational, and financial outcomes with innovative solutions that advance the next generation of care. Our mission is to contribute to creating a healthier world. | 6/16/2023 |
| 4582 | Eli Lilly Cambridge, MA Biologist - Neuroscience Research BSc or MSc in Neuroscience, biological sciences or related fields. Exp: 1+ years |
The Next Generation Therapeutics group is a newly formed team with a focus on using novel therapeutic modalities to deliver medicines for chronic pain and neurodegenerative disorders. The group, based at our Cambridge Innovation Center in Kendall Square, will work with internal and external partners to identify and deliver new novel therapies into patients at speed. The team is seeking experienced and inspiring scientists to join our fast-paced, interdisciplinary team as we leverage innovative RNA/oligonucleotide/gene and genomic based therapeutic modalities to enhance our portfolio. | 6/16/2023 |
| 4583 | Eli Lilly Indianapolis, IN Process Control Engineer Master's degree in Engineering or technology related degree. Exp: 1 year |
The Process Control Engineer provides automation support for manufacturing operations in accordance with appropriate GMP and safety guidelines. This support includes change control implementation, deviation investigation, routine automation computer system support activities, and off hours automation computer system support. The Process Control Engineer also leads non-routine automation computer system support activities, delivers engineering projects to the business, is able to utilize first principles in delivery of these solutions, and can recommend new control strategies for the various chemical processes utilized in manufacturing operations. | 6/16/2023 |
| 4584 | Organogenesis Canton, MA QC Analyst I/II -Microbiology AS or BS degree in a Biology, Chemistry. Exp: 1+ years |
The purpose of this position is the performance and reporting of microbiological testing for product release as well as environmental monitoring of all areas of the manufacturing facility, water sample collection and testing, compilation and entry of environmental monitoring data. The position ensures that the company goals for timely product testing are accomplished by being directly involved in the production of test results for product release and investigations. Other responsibilities or tasks as deemed necessary from time to time by the area’s supervisor. | 6/16/2023 |
| 4585 | Organogenesis Canton, MA Production Associate I - Apligraf Associates or Bachelor’s degree in biology or related science. Exp: 0 - 2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 6/16/2023 |
| 4586 | Meridian Medical Technologies Groton, CT Associate Scientist, Medicinal Chemistry Bachelor’s Degree in chemistry. Exp: 0 to 2 years |
At Pfizer we deliver breakthroughs that change patients’lives. In this job, you'll be joining a team which plays a vital role in this mission through the discovery of Pfizer’s small molecule and syntheticallyderived drugs. In your work, you will be joining a team comprised of experts in the major scientific disciplines involved in the discovery and preclinical development of small molecule drugsincludingmolecular design, synthesis, computational chemistry, pharmacology, chemical biology, structural biology, biophysics, DMPK and analytical chemistry. You will be assisting with the delivery of high-quality drug candidates into the clinic, establishing new drug design approaches and principles, and developing synthetic innovations that drive medicinal chemistry strategies. As an Associate scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 6/16/2023 |
| 4587 | Meridian Medical Technologies Pearl River, NY Associate Scientist - Robotics and Automation, Vaccines R&D Bachelor's Degree in?a relevant field of science (biomedical engineering, biology, immunology, microbiology, etc.). Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to participate and operate robotic units in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support downstream analyst by doing sample preparation and starting the lifecycle of a sample. You will also spearhead new and innovative projects for process improvement and upkeep of the laboratory. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 6/16/2023 |
| 4588 | Meridian Medical Technologies Pearl River, NY Associate Scientist - Robotics & Automation, Vaccines Bachelor's Degree in a related Science field. Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of executing robotic sample preparation in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 6/16/2023 |
| 4589 | Meridian Medical Technologies Pearl River, NY Associate Scientist Bachelor's Degree in a related Science field. Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of executing robotic sample preparation in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 6/16/2023 |
| 4590 | Meridian Medical Technologies McPherson, KS Chemist I (AB2 shift/ 12 hour night shift) Bachelor's Degree in Chemistry or related science field. Exp: 0-1 years |
As part of the Technical Operations team, you are recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations. You will train others and reinforce behaviors that will help us achieve our goal of providing the best healthcare to our patients. | 6/16/2023 |
| 4591 | Meridian Medical Technologies McPherson, KS Microbiologist BS/MS in Microbiology or related scientific field. Exp: 0-2 years |
The BQ Lab Analyst I, will perform basic analysis for raw materials, in process and/or finished products in a safe, compliant, and efficient manner. The Job responsibilities include performing microbiological and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality. | 6/16/2023 |
| 4592 | Meridian Medical Technologies Rocky Mount, NC Environmental Control Analyst II - Day Shift Bachelor’s Degree in Biology, Microbiology, Chemistry, or similar field. Exp: 0+ years |
You will be a team member who is relied to have a good understanding of procedures, techniques, tools, materials and equipment. Your decision making will help you prioritize workflows based on the available resources. You will follow standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. You will contribute to the team’s success by sharing your previously acquired knowledge. | 6/16/2023 |
| 4593 | Regeneron Tarrytown, NY Assoc. Scientist, Protein Development BS or MS Exp: 0-3+ years |
Regeneron's Protein Development group, a part of our Therapeutic Proteins organization, and located in Tarrytown, NY is seeking an Associate Scientist. In this role, you will drive biochemical characterization of protein reagents and antibodies in support of the company’s VelocImmune fully human antibody pipeline and Immune Oncology programs. | 6/16/2023 |
| 4594 | Regeneron Tarrytown, NY Associate Scientist, Protein Biochemistry BS or MS in Biophysics, Biochemistry, Chemical Engineering, or related field. Exp: 0-2 years |
Regeneron's Protein Biochemistry group, located in Tarrytown is seeking an Associate Scientist who will be responsible for providing in-depth characterization of therapeutic proteins to support research, and late-stage development of various programs. In this exciting role you will be encouraged to participate in method development and technology innovation efforts aimed to improve our understanding and characterization of biotherapeutic proteins. | 6/16/2023 |
| 4595 | Regeneron Tarrytown, NY Associate Scientist, Protein Expression Sciences (PES) M.S. in Molecular Biology, Cellular Biology, Biology or related field. Exp: 0-2 years |
Regeneron is looking for an Associate Scientist to join the Protein Expression Sciences team. | 6/16/2023 |
| 4596 | Regeneron Tarrytown, NY Associate Scientist, Immunology/In Vivo (VI Next) MS in molecular biology, immunology, or related fields. Exp: 0-5 years |
Our group develops and optimizes Regeneron’s mouse platform technologies producing human antibodies and other alternative antibody-based formats. We are seeking and experienced Associate Scientist to join our team to help with cloning projects as well as in vivo mouse immunization and B cell characterization work. | 6/16/2023 |
| 4597 | Regeneron Tarrytown, NY Assoc Scientist, Clinical Bioanalysis BS degree or MS degree in a scientific field. Exp: 0-3+ years |
Regeneron's Clinical Bioanalysis group, located in Tarrytown NY, is seeking an Associate Scientist. | 6/16/2023 |
| 4598 | Aptevo Therapeutics Seattle, WA Assistant Scientist I / II - Immunobiology BS/BA or Master’s degree. AALAS ALAT certification or comparable experience equivalent desired or willing to achieve certification within 6 months of Exp: 1+ years |
The Immunobiology group is seeking an experienced Assistant Scientist to support therapeutic product development by characterizing the biologic activity of bispecific protein therapeutics in pre-clinical research using in vitro and in vivo experimental approaches. She/he will develop and conduct in vitro and ex vivo cellular assays to screen and characterize candidates. Will participate in the planning, execution, analysis, and documentation of experiments. Will work in a collaborative group to provide animal husbandry and maintenance support. Work carefully with in vivo oversight to ensure high quality and compliance. This position will work collaboratively with colleagues across functional groups to provide basic support to pre-clinical research programs. Perform assigned experiments under close or general supervision. Plan and organize details of experiments and keep accurate records. Collaborate with supervisor to develop routine methods. May independently draft basic experimental plans for review with supervisor. Work impacts tasks or initiatives within own group. Provide progress updates to supervisor. | 6/7/2023 |
| 4599 | Arbor Biotechnologies Cambridge, MA Research Associate, Genomic Editing Characterization BS Degree Exp: 0-2 years |
The Arbor Biotechnologies preclinical team is looking to hire a motivated Research Associateto characterize the effectiveness and safety of our novel and proprietary CRISPR-based gene editors.This candidate will help plan, execute, and interpretexperiments that will be used to build Arbor’s portfolio of genetic medicines.He/she/they will have the opportunity to work on multiple lead programs targeting liver and CNS indications. | 6/7/2023 |
| 4600 | Arbor Biosciences Ann Arbor, MI Technical Specialist, Genomics Required: Bachelor’s degree in related field and job experience in life sciences / biotechnology. Preferred: Master’s degree in related field and / or Exp: 1-year |
The Technical Specialist, Genomics is responsible for technical conferrals and support for the Daicel Arbor Biosciences genomics tools and services portfolio, currently including next-generation sequencing kits (myBaits) and laboratory/bioinformatics services (myReads) and cytogenetic probes (myTags). This individual is a core team member supporting Daicel Arbor Biosciences’ essential genomics custom products/services business. This detail-oriented individual should enjoy working with researchers around the world to successfully and efficiently advance their project goals with Daicel Arbor Biosciences products/services. In this role, they serve as a key liaison between clients, account representatives, and internal technical specialty teams. They are knowledgeable about technical applications and scientific usage of Daicel Arbor Biosciences’ NGS and cytogenetics products/services and are able to apply and communicate this knowledge productively to internal and external stakeholders. As needed, they serve as primary technical point of contact for genomics orders that involve technical discussion and/or customization. | 6/7/2023 |
| 4601 | Arrowhead Pharmaceuticals San Diego, CA Research Associate/Associate Scientist, Histology Bachelor in Cell Biology, Molecular Biology, Biochemistry or a related discipline or HT license. Exp: 1-2 years |
The Research Associate/Sr. Research Associate is a member of the Histotechnology team in the Toxicology Department. The Histotechnology team supports the Company’s preclinical drug development efforts by designing studies, collecting, preparing and analyzing samples generated by the Company’s animal studies. The candidate works under the direction of the team lead and employs a wide range routine and non-routine histological methods and analyses. | 6/8/2023 |
| 4602 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, CMC Process Development BS/BA in Chemistry or related field. Exp: 1 year |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Chemist to work as a Chemist in the Chemistry, Manufacturing, and Controls Group focusing on small molecule process development. This is an ideal position for an individual with an organic chemistry background who has an interest in projects related to novel technology in the synthesis and purification of small molecules and bioconjugates. | 6/8/2023 |
| 4603 | Arrowhead Pharmaceuticals Madison, WI Associate Production Chemist (1st shift) Bachelor’s degree in a scientific field. Exp: Entry level to 5 years |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for a 1st Shift Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. | 6/8/2023 |
| 4604 | Arrowhead Pharmaceuticals Madison, WI Associate Production Chemist (2nd shift) Bachelor’s degree in a scientific field. Exp: Entry level to 5 years |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for a 2nd Shift Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. 2nd shift work hours are 1 pm – 11:30 pm and include a 12% shift differential. | 6/8/2023 |
| 4605 | Ascent Pharmaceuticals Central Islip, NY Analytical Chemist Bachelor’s degree or foreign equivalent in Pharmacy/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Analytical Chemists for our Central Islip, NY location to develop, validate and conduct inter laboratory transfer of analytical methods for active pharmaceutical ingredients (API) and dosage forms; validate analytical methods and perform quality control activities; research & develop efficient and selective analytical procedures and draft/review laboratory SOPs; design, evaluate and monitor stability programs for drug products; work with advanced analytical equipment; supervise and train chemists and laboratory personnel; test drug substances, intermediates and raw materials while conducting impurity profiles for drug substances and intermediates; prepare ANDAs for FDA submissions etc. | 6/8/2023 |
| 4606 | Ascent Pharmaceuticals Central Islip, NY Manufacturing Chemist Bachelor’s degree or foreign equivalent in Pharmacy/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Manufacturing Chemist for our Central Islip, NY location to plan & coordinate activities related to manufacturing of various dosage forms; develop pharmaceutical dosage forms using advanced scientific techniques; develop new process concepts for product optimization and yield improvement; implement monthly production plans & generate monthly reports; perform IQ, OP & PQ of production equipment; work with product development team to execute bio-batches & validation batches; develop SOPs; draft submissions to regulatory agencies etc. | 6/8/2023 |
| 4607 | Ascent Pharmaceuticals Central Islip, NY Quality Control Chemist Bachelor’s degree or foreign equivalent in Pharmacy/ Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Quality Control Chemists in our Central Islip, NY location to perform pharmaceutical laboratory quality control/development activities; develop and validate analytical methods; analyze raw materials and in-process/finished product samples using modern QC techniques; develop/implement & maintain QC systems & activities using advanced analytical lab equipment/ instrumentation; validate & analyze results as per USP, BP, EP, ICH and USFDA guidelines; perform in-process inspections; prepare/implement SOPs; analyze scientific data and prepare detailed QC reports; research, draft and prepare submissions & responses to FDA; update pharma lab equipment/ instrumentation inspection procedures & checklists as necessary etc. | 6/8/2023 |
| 4608 | Ascent Pharmaceuticals Central Islip, NY Quality Assurance Chemist Bachelor’s degree or foreign equivalent in Science/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Quality Control Chemists in our Central Islip, NY location to collaborate with multiple departments including Manufacturing, Facilities, Engineering, Quality Control, Validation, Quality Assurance, and Regulatory to facilitate agreement on equipment, initiation and execution of Product development projects (ANDA Projects), process operational parameters, test requirements and acceptance criteria; Execute Change Controls to allow for the ongoing maintenance and optimization of validated systems and report KPI’s to higher management; Review and approve of a variety of validation lifecycle documents, project plans, user requirement specifications, SOPs, maintenance documentation, investigation reports, deviation resolution, CAPA closeout, etc.; Conduct internal & vendor audits in a group setting & under guidance from senior chemists/scientist for compliance with SOP, CGMP & FDA requirements. Research new regulatory guidance and cGMP and prepare reports for senior scientists and department heads to review and assist in drafting SOP’s; Critically evaluate current processes and continually identify ways to save time and money without sacrificing product quality; Investigate product, and process deviations, identify root cause, and develop corrective and preventative actions; Participate in audits by customers and regulatory agencies and respond to customer complaints in timely manner, review and close out market enquiries & investigations; Assist in APQR, Deviation & Investigation, Risk Assessment, CAPA Management, Change control management, Root Cause Investigation with SPC tools, Market Complaint Handling, Adverse event investigations; Review and Report Process Characterization Protocols, Equipment Qualifications, and review Process Validations of various ANDA drug projects; Conduct internal audits for compliance with SOP, cGMP & FDA requirements. | 6/8/2023 |
| 4609 | Asha Pharma San Diego, CA SR./RESEARCH ASSOCIATE (SAN DIEGO, CA) BS/MS degree in Chemical Engineering, Materials Science, Chemistry, Pharmaceutical Science or related field. Exp: 0-2 years’ |
This position involves working in a laboratory that evaluates novel chemical compounds (typically pharmaceuticals) and discovers novel crystalline structures of the same as part of drug development. The Sr./Research Associate will independently work on projects related to crystallization R&D (e.g. polymorph, salt, cocrystal screening and crystallization process development for pharmaceutical and other molecules) under the guidance of a senior team member. The Sr./Research Associate will also help with Business Development Activities, providing a unique opportunity for well-rounded career development. This position involves working in a laboratory that evaluates novel chemical compounds (typically pharmaceuticals) and discovers novel crystalline structures of the same as part of drug development. | 6/8/2023 |
| 4610 | Astellas South San Francisco, CA Analyst I, QC Microbiology Bachelor’s Degree in chemistry, biology, or microbiology. Exp: 0-3+ years’ |
The primary purpose of the Analyst I position is to Support Quality Control Microbiological testing of drug substances, raw materials, and process intermediates in support of clinical development and commercial programs under cGMP and GLP guidelines. | 6/8/2023 |
| 4611 | Astellas Sanford, NC QC Biochemical Analyst I BS. degree in Biological Sciences. Exp: 0-2+ years |
Analyst I, QC Biochemical, will be responsible for implementing and executing analytical testing in support of clinical and commercial viral vector products in compliance with GMP requirements. Will also support testing for stability studies, methods validation studies and equipment validation. | 6/8/2023 |
| 4612 | Astellas Sanford, NC Analyst I, QC Microbiology BS. degree in Microbiology or other science related degree. Exp: 0-2+ years |
Analyst I QC Microbiology will be responsible for implementing and executing microbiological testing in support of clinical and commercial products in compliance with GMP requirements. This role will also support testing for stability studies, methods validation studies and equipment validation. | 6/8/2023 |
| 4613 | Astellas Seattle, WA Research Associate II, Clinical Gene Editing MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 6/8/2023 |
| 4614 | Astellas Seattle, WA Research Associate II, Clinical Gene Editing MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 6/8/2023 |
| 4615 | Astellas South San Francisco, CA Research Associate II, Discovery Biosciences Master’s Degree in Molecular Biology, Biology, Life Sciences, or a related discipline Exp: 1+ years |
The Research Associate will support the Discovery Bioscience team and assist in developing and executing screening assays for the evaluation of AAV vector products. The Research Associate will be located in our South San Francisco R&D laboratories. | 6/8/2023 |
| 4616 | Astellas South San Francisco, CA Research Associate II, Vector Biosciences Master’s Degree in Molecular Biology, Cell Biology, Life Sciences or a related discipline. Exp: 1+ years |
The Research Associate II will support activities within the Discovery Biology Department. This position involves application of several techniques to produce, purify and characterize AAV viral vectors. The Research Associate will be located in our South San Francisco R&D laboratories. | 6/8/2023 |
| 4617 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters Exp: 0-1 year |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 6/8/2023 |
| 4618 | Axial Therapeutics Woburn, MA Research Associate/Senior Research Associate - Biosciences Bachelor’s degree in biology, biochemistry, or a related field preferred. Exp: 1-3 years |
In this role the Research Associate will support biology as a member of a highly matrixed drug discovery team and will be responsible for the execution and troubleshooting of various cell-based and biochemical assays and experiments. The Research Associate will contribute to drug screening and mechanism-of-action studies for projects in immuno-oncology and neurological diseases and disorders and have opportunities to contribute to new target discovery and validation. This proactive researcher will collaborate with team members, identify opportunities to improve efficiency, share ideas and expertise and contribute to Axial’s creative, dynamic, and collaborative culture. | 6/8/2023 |
| 4619 | Axis Clinicals USA Dilworth, MN Analytical Chemist I Bachelors degree in Biology, Chemistry, or equivalent. Exp: 1 year |
The Analytical Chemist I, Bioanalytical Operations carries out various Bioanalytical functions of the organization. The Analytical Chemist is responsible for executing Bioanalytical methods within AXIS Clinicals. | 6/8/2023 |
| 4620 | Berkshire Sterile Manufacturing Lee, MA Manufacturing Process Engineer Bachelors’ of Science in Chemical Engineering, Chemistry, Biology or Pharmaceutical Science required or Masters’ in Chemical Engineering, Chemistry, B Exp: Six plus (6+) months |
The Manufacturing Process Engineer will collaborate Process Engineering with tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role is to deliver effective, safe and optimized manufacturing processes for parenteral drug products. | 6/8/2023 |
| 4621 | Berkshire Sterile Manufacturing Lee, MA Process Engineer Process Engineer: Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science. Exp: One (1) to three (3) years |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 6/8/2023 |
| 4622 | Biocare Medical Pacheco, CA Associate I, Polymer Qualification Bachelor of Science Degree in Biology or a related field. Exp: zero to five (0-5) years’ |
The Associate I, Polymer Qualification functions with minimal supervision and guidance within the research and development (R&D) laboratory. Associate I, Polymer Qualification performs R&D activities on new and existing products involving Immunohistochemistry (IHC) and Protein Chemistry Quality Control (QC) procedures within well-defined guidelines. Associate I, Polymer Qualification keeps abreast of current methodologies and developments within defined areas of research. Antibody Qualification Associate participates in collaborative projects, and at times, assist other laboratory members on research-related activities. | 6/9/2023 |
| 4623 | Biological Dynamics San Diego, CA Research Associate I Bachelor's degree in a scientific discipline. Exp: Entry Level |
The Research Associate is a hands‐on role tasked with experimental work, data acquisition, and basic analysis supporting development of the Company’s proprietary technology programs focused on cancer, neurological, and infectious disease detection. As part of the Research Team, the Research Associate performs studies, supporting the research and development of novel biomarker assays. The Research Associate contributes to the planning, execution, and data analysis of studies under the guidance of senior scientists, supporting growth of IVD products through feasibility to development stages. This hands-on position provides the opportunity to contribute to the development of RUO/LDT products based on an innovative diagnostic platform as part of our growing company. | 6/9/2023 |
| 4624 | Biological Dynamics San Diego, CA Research Associate II Master's degree in Biochemistry, Bioengineering or a related field. Exp: Mid Level |
The Research Associate II is a hands‐on role tasked with experimental work, data acquisition, and basic analysis supporting development of the Company’s proprietary technology programs focused on cancer, neurological, and infectious disease detection. The Research Associate II performs studies supporting the research and development of novel biomarker assays. This position contributes to the planning, execution, and data analysis of studies under the guidance of senior scientists, supporting growth of IVD products through feasibility to development stages. This hands-on position also contributes to the development of RUO/LDT products based on an innovative diagnostic platform as part of our growing company. | 6/9/2023 |
| 4625 | Biomerics Salt Lake City, UT Process Engineer Engineering Degree needed. Exp: 1-3 years |
The Process Engineer will be responsible for supporting and improving the manufacturing of class II medical and surgical devices in a dynamic, customer-focused organization. You will be expected to work with customers to understand product and process specifications, develop manufacturing processes, and build and test devices to those specifications. All activities will be expected to be documented according to design control requirements in a design history file (DHF). The Process Engineer may function as an individual contributor in a small cross-functional team comprised of engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. You will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team. | 6/9/2023 |
| 4626 | Novozymes Salem, VA Research Assistant I - Salem, VA Requires a Bachelor's Degree in a scientific discipline. Exp: 1+ years |
Join us as our new Research Assistant Are you ready for a challenging role that lets you use both your scientific grounding and communication skills? Do you have a passion for science and enjoy solving problems that lead to the launch of new products? If so, you could be the Research Assistant we’ve been looking for who can work within the internal process development group, as well as with outside units, to develop advanced and scalable fermentation, recovery, and formulation processes for both existing and novel microbe-based products (i.e., bacteria, fungi, and yeast). This individual will use their in-depth understanding of the scientific principles of microbial fermentation, recovery, formulation, and process development to pioneer research and transform it into value-added products. | 6/9/2023 |
| 4627 | Shape Therapeutics Seattle, WA Research Associate/Sr. Research Associate BS/MS degree in Neuroscience, Molecular/Cellular Biology or related discipline. Exp: 1-3 years |
ShapeTX is looking for a highly motivated and scientifically curious individual to join the Pipeline Research team as a Research Associate / Senior Research Associate. In this role, the successful candidate will primarily conduct in vitro cell-based assays to evaluate novel candidate therapeutics from the ShapeTX RNAfixTM and RNAswapTM technology platform. An ideal candidate will have general cellular and molecular biology experience, a teachable and collaborative spirit, and a desire to work in a fast-paced start-up environment. Neuroscience experience is a plus. This is an excellent opportunity to join the Pipeline Research team and advance the next generation of transformative gene therapies towards the clinic. | 6/9/2023 |
| 4628 | Boston Analytical Salem, NH QC Microbiologist BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 6/9/2023 |
| 4629 | Boston Analytical Salem, NH Raw Materials Analytical Chemist I Bachelor’s degree in Chemistry or a related discipline is required. Exp: 0-2 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties include performing analysis of Raw Materials using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development according to USP/EP methods. | 6/9/2023 |
| 4630 | Boston Analytical Salem, NH Microbiologist - Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 6/9/2023 |
| 4631 | Boston Analytical Salem, NH CHEMIST I Bachelor’s degree in Chemistry or a related science discipline is required. Exp: 0-2 years |
The Analytical Chemist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 6/9/2023 |
| 4632 | Boston Analytical Framingham, MA Microbiologist EM FTE BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The Environmental Monitoring Microbiologist conducts cleanroom monitoring activities to ensure the air, surfaces, and critical utilities utilized for pharmaceutical product manufacturing meet cGMP requirements. These samples are collected according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. | 6/9/2023 |
| 4633 | Boston Institute of Biotechnology Southborough, MA Research Associate Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≤1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision. | 6/9/2023 |
| 4634 | Boston Institute of Biotechnology Southborough, MA Upstream Process Development Research Associate BS degree in Biochemical Engineering or related field of study. Exp: 0-2 years |
Responsibilities 1. Set up, execute, and monitor microbial and mammalian cell culture production in fermenters and bioreactors. 2. Collect, record, and report experimental data. 3. Provide updates to a team lead on a regular basis. 4. Maintain all notebooks and documentation according to department standards. 5. Write SOPs, and batch records. 6. Ability to work well in a team environment and independently as required. 7. Ensure and promote safe environmental and laboratory practices. 8. Order supplies as needed. 9. Prepare solutions and buffers. 10. Maintain lab space and equipment. | 6/9/2023 |
| 4635 | Boston Institute of Biotechnology Southborough, MA Research Associate Analytical Development Bachelor’s or Master’s degree in Biology, Chemistry, Pharmaceutical Sciences, or a related/relevant discipline or demonstrated coursework in such area Exp: Entry Level |
The Research Associate role within Analytical Development is an entry level position for individuals with a Bachelor’s or Master’s degree. Responsibilities include developing analytical methods for biologics characterization, characterizing samples from process development, and supporting subsequent clinical and/or commercial GMP manufacturing. | 6/9/2023 |
| 4636 | BostonGene Waltham, MA Research Associate, Molecular Biology & Next Generation Sequencing Bachelor’s (B.S.) degree in biology, clinical laboratory science, medical technology, or related discipline. Exp: 0-2 years |
ostonGene is seeking a highly motivated Research Associate to join our R&D team in our laboratory located in Waltham, MA. This candidate will support BostonGene’s state-of-the-art primary next-generation sequencing (NGS), adjunct analytical platforms, and automated analysis pipelines. The candidate will be expected to develop proficiencies in NGS support protocols, such as RNA and DNA isolation from tissue, cell-free DNA isolation from plasma, Whole Exome and RNA-Seq library preparation, qPCR, Molecular Biology techniques, and other sample QC techniques. | 6/9/2023 |
| 4637 | BPS Bioscience San Diego, CA Research Scientist I - Cell Biology M.S. Exp: 1+ years |
Perform basic molecular biology, lentivirus production, and stable cell line generation conduct cell-based reporter assays with luciferase and fluorescence as the readout contribute to the development of new lentivirus and cell line products and cell-based assays. | 6/9/2023 |
| 4638 | Alexza Pharmaceuticals Fremont, CA QC Analyst II Master’s degree in science or related field. Exp: 1 year |
Provide timely analyses to support manufacturing and stability. Primary responsibilities include but not limited to physical testing of components and raw materials, in process and release of commercial product or clinical supplies Independently perform assays under GMP, maintaining data integrity and ensuring compliance with company SOPs and specifications Provide accurate, written documentation of all work, including detailed observations and conclusions. Under general guidance, participate in laboratory investigations Independently operate, maintain and troubleshoot laboratory instrumentation and equipment in a safe working environment | 5/31/2023 |
| 4639 | Aptitude Medical Systems Santa Barbara, CA Research Associate Bachelor’s degree or Master’s degree in a relevant discipline. Exp: Entry-Level |
We are seeking to hire multiple capable and driven entry-level Research Associates to join our tight-knit research and development team. In this position, you will be working closely with a cross-functional team of mission-driven scientists and engineers to drive the invention and development of novel diagnostic products. | 5/31/2023 |
| 4640 | Avidity Biosciences San Diego, CA Research Associate, Chemistry BS or MS in chemistry, biochemistry, chemical engineering, or related discipline Exp: 1+ years |
We are seeking a Research Associate to join our team in La Jolla. This is a hands-on position with responsibility for the design, synthesis, and analysis of antibody oligonucleotide conjugates. The ideal candidate will have biotech/pharma experience in aspects of medicinal chemistry, bioconjugation and nucleic acid therapeutics. The candidate is expected to be a strong team player, who enjoys scientific discovery and can communicate and collaborate in an interdisciplinary environment. | 5/31/2023 |
| 4641 | Bio-Concept Laboratories Indianapolis, IN Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4642 | Bio-Concept Laboratories Huntington Beach, CA Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4643 | Bio-Concept Laboratories Redding, CA Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4644 | Bio-Concept Laboratories Woburn, MA Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4645 | Bio-Concept Laboratories Baton Rouge, LA Scientist 1 Associate's degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4646 | Bio-Concept Laboratories Pittsburgh, PA Microbiologist - Scientist Bachelor’s degree in Microbiology, Biology, Chemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the microbiology department of our environmental testing laboratory. | 6/1/2023 |
| 4647 | Bio-Concept Laboratories Springfield, MO Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4648 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline. Exp: 1 to 6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 6/1/2023 |
| 4649 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 6/1/2023 |
| 4650 | CRISPR Therapeutics Boston, MA Research Associate II MS degree in Chemistry, Chemical Engineering, Biochemistry, Bioengineering, Pharmaceutical Sciences or related field. Exp: 0+ years |
We are seeking an experienced Research Associate II to support our analytical biochemistry team. The successful candidate will leverage their technical expertise in analytical chromatography and mass spectrometry to advance our gene editing platform by providing key insights into the synthesis, impurity profile, purification, and structure-activity relationships of oligonucleotides, including gRNA. | 6/1/2023 |
| 4651 | CRISPR Therapeutics Boston, MA Research Associate II, Oligonucleotide Synthesis MS degree in Chemistry, Chemical Engineering, Biochemistry, Bioengineering, Pharmaceutical Sciences or related field. Exp: 0+ years |
CRISPR Therapeutics is seeking a highly motivated Research Associate to join our In Vivo Technical Operations department in Boston, Massachusetts. The incumbent will be responsible for the oligonucleotide synthesis, purification, desalting, and analysis to support the process development of guide RNA production in various scales. This position will also support therapeutic programs in multiple disease areas in R&D department. Prior experience in oligonucleotide synthesis, purification, and characterization is desired. | 6/1/2023 |
| 4652 | CRISPR Therapeutics Framingham, MA Manufacturing Associate Bachelor's degree in biological sciences or related fields. Exp: 1-5 years |
Reporting to the Manufacturing Supervisor, the Manufacturing Associate will perform manufacturing activities associated with immuno-oncology GMP manufacturing within a state-of-the-art manufacturing facility at 33 New York Ave in Framingham, MA. A successful candidate will be responsible for the manufacture of allogenic gene edited cell therapies for clinical studies and as a commercial product. This role requires clear communication across multiple departments for the execution of daily activities. The ideal candidate will have experience successfully performing aseptic cell culture within a GMP environment. | 6/1/2023 |
| 4653 | CRISPR Therapeutics San Francisco, MA Research Associate II, CRISPR-X MS in biology or related disciple. Exp: 0-2 years |
We are seeking a Research Associate II to join the CRISPR X group at CRISPR Therapeutics, the leading gene editing company. The successful candidate will be an integral part of a team whose aim is to advance next generation gene editing. The position requires enthusiasm, passion, attention to detail and a desire to assist in developing the next generation of gene editing. | 6/1/2023 |
| 4654 | Invivotek Hamilton Township, NJ Research Associate (In Vivo/Animal Science) Bachelor of Science degree in Life Science required, Master Degree (Preferred) Exp: 1 to 2 years |
We are seeking a highly motivated and talented individual to join our preclinical in vivo oncology and disease associates’ team. The individual will perform in vivo bioassays on mice and rats in a fast-paced, team-oriented collaborative environment. The candidate should have exceptional skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Should have a strong foundation in in vivo oncology & disease models. Excellent communication and computer skills. Attention to detail with organizational and record keeping skills. Motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. Must maintain a professional demeanor and be able to take necessary initiative to meet project timelines and deliverables. | 6/1/2023 |
| 4655 | Invivotek Hamilton Township, NJ Research Associate B.S or M.S. in Molecular Biology, Biochemistry, or a related field. Exp: 1+ years |
Ingenio Diagnostics, a GD3 company, is seeking a motivated Research Associate to support client-driven molecular biology services in Hamilton, NJ. | 6/1/2023 |
| 4656 | Invivotek San Francisco & Sunnyvale, CA Research Associate BS degree in a scientific field. Exp: 1+ years |
Comparative Biosciences, Inc(CBI) a part of Genesis Biotechnology Group is in need of a Research Associate that will assist and execute scientific studies performed at CBI. This will include performing clinical observations of animals and the essential duties and responsibilities required by the facility. | 6/1/2023 |
| 4657 | Invivotek Sunnyvale, CA Research Associate I BS degree in a scientific field. Exp: 1+ years |
Comparative Biosciences, Inc, a member of Genesis Biotechnology Group is looking to grow our team in the Sunnyvale, CA area. We are currently looking for a full time Research Associate I. The ideal candidates for the Research Associate l will assist and execute scientific studies performed at CBI. This will include performing clinical observations of animals and the essential duties and responsibilities required by the facility. | 6/1/2023 |
| 4658 | Invivotek Sunnyvale, CA Research Associate II BS degree in a scientific field. Exp: 1+ years |
Research Associate will assist and execute scientific studies performed at CBI. This will include performing clinical observations of animals and the essential duties and responsibilities required by the facility. | 6/1/2023 |
| 4659 | Invivotek Hamilton , NJ Research Associate I Bachelor of Science degree in Life Sciences. Exp: 1 to 2 years |
We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 6/1/2023 |
| 4660 | Nano Precision Medical Emeryville, CA Analytical Chemist Master’s Degree in chemistry, analytical chemistry, or equivalent discipline. Exp: 1+ years |
This role requires an experienced hands-on analytical chemist who flourishes in a fast-paced start-up environment with shifting priorities and evolving requirements. The AC team provides ongoing analytical services to the R&D and Manufacturing teams, and also develops and transfers new analytical methods and performs one-off special investigations and projects. You’ll be part of a close-knit team of people who are focused, driven, and willing to do whatever it takes to keep the department running. The role requires strong team orientation, flexibility, excellent communication skills, attention to detail, and creative problem solving. | 6/2/2023 |
| 4661 | PL Developments Miami, FL Analytical Scientist I BS or MS in Chemistry Exp: 1-3 years |
Performs testing on raw material, in-process & finished product samples Executes method transfer, verification and validation protocols Documents all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines Evaluate and interpret the test results and other related technical documentation Writes methods and reports | 6/2/2023 |
| 4662 | Tanvex BioPharma San Diego, CA Research Associate, Cell Culture Process Development - #1358 BS or advanced degree in chemical/biochemical engineering, cell biology, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Cell Culture Development is responsible for executing individual experiments related to all aspects of cell culture process development of biopharmaceuticals, including media preparation, bioreactor setup, cleaning, sterility and operation, maintaining instruments and equipment, examining data and preparing experiment reports. Applies basic engineering and scientific principles to perform trouble-shooting of processes, instrumentation, and equipment. | 6/2/2023 |
| 4663 | Acceleron Pharma Kenilworth, NJ Scientist, Biologics Analytical Research and Development M.S. in analytical chemistry/biochemistry or related field. Exp: 1+ years |
The Biologics Analytical Research & Development department of our Research & Development Division is seeking applicants for a Scientist position available at its Kenilworth, New Jersey research facility. The Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of Biologics drug substances and drug products. The successful candidate should function well and be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. The qualified candidate will be responsible for development, qualification, implementation, troubleshooting and transfer of analytical methods for monoclonal proteins or other complex therapeutic proteins. Applicants should have effective organizational, multi-tasking, oral/written communications skills, show scientific leadership, and a desire to conduct research and publish. Evidence of strong cross-functional collaboration in an academic or industrial setting is also preferred. | 6/2/2023 |
| 4664 | Acceleron Pharma West Point (PA); Rahway (NJ), PA Scientist - Fermentation, Novel Expression Systems MS with relevant academic or thesis experience in biological engineering, biotechnology, biological science, microbiology, or related field. Exp: 1+ years |
As a member of the Fermentation team in Novel Expression System group, the applicant will serve as an individual scientific contributor as part of a team responsible for bioprocess development and optimization of various expression systems for enzymes, vaccines, and other bioproducts. The candidate is also expected to carry out collaborative research supporting the implementation of these methodologies which involves conceiving, designing, and executing process development experiments. A successful candidate should also have excellent interpersonal, communication and collaboration skills and maintain a focused attention on laboratory safety for everyone on the team. | 6/2/2023 |
| 4665 | Acceleron Pharma West Point , PA SCIENTIST/ENGINEER – UPSTREAM VACCINE PROCESS DEVELOPMENT M.S. in Engineering: Chemical Engineering, Bioengineering, Biomedical Engineering; M.S. in Science and Technology: Cell Biology, Biological Sciences, Exp: one (1) year |
Applications are sought for an opportunity in the Vaccine Process Development (VPD) department, which is part of Our Company's Research Labs division. The individual will support our company's discovery & development efforts for Vaccine programs at West Point, PA. The successful candidate is expected to work with other upstream scientists and engineers, typically focusing on one to two vaccine programs at a time. The candidate will have the ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude. The candidate will have the ability to learn new techniques, to balance multiple projects, to keep accurate records, to follow instructions, and to comply with company policies. The successful candidate will possess proven ability to work in a hands-on laboratory setting and excellent organization, interpersonal, verbal, and written communication skills. | 6/2/2023 |
| 4666 | Acceleron Pharma West Point, PA Associate Specialist, Engineering B.S. or B.A. in Mechanical or Chemical Engineering degree or other science degree Exp: Six plus months |
The Associate Vaccine Manufacturing Technical Support Specialist will provide engineering technical support to the manufacture of liquid vaccines. The role is focused on technical services support with primary focus in the areas of customer complaints, and deviation investigations. The role also encompasses technical services support with primary focus in the areas of deviation management, validation and product franchise support. Specific assignments maybe focused in one area or span across multiple areas of focus. | 6/2/2023 |
| 4667 | Acceleron Pharma Elkhorn, NE Associate Scientist Biology-Discovery Bachelor's degree in biology, microbiology, virology, immunology, or related field. Exp: 1-2 years |
This is primarily a site-based role, under the direction of a supervisor, to conduct laboratory and animal studies for the development of new or improved veterinary or biological products. | 6/2/2023 |
| 4668 | Acceleron Pharma Kenilworth (NJ); Rahway (NJ), NJ Senior Technician Bachelors degree in a related discipline. Exp: 0+ years |
In this role you are expected to work in a team atmosphere in close collaboration with BioProcess development scientists, facility engineering, lab automation and safety groups. We will provide you the necessary on the job training needed to perform laboratory activities. Throughout your career, we will offer you continued development through training classes, workshops, meetings, etc., to improve job skills and product-related procedures. | 6/2/2023 |
| 4669 | Acceleron Pharma Elkton, VA Vaccine Manufacturing Laboratory Technician Bachelor degree. Exp: 1+ years |
The Vaccine Manufacturing Laboratory Technician will work in Technical Operations in support of various Bioprocesses, Fermentation, Biologics Manufacturing, Vaccines Manufacturing, and Wastewater Analysis. | 6/2/2023 |
| 4670 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Stem Cell & Gene Therapy Master’s degree in a related field. Exp: up to 2 years |
The Stem Cell and Gene Therapy Advanced Research Associate will be part of a team responsible for the design and development of novel products used in cell and gene therapy workflows, including tools for expansion, identification, and differentiation of immune cells from pluripotent stem cells. Preference will be given to candidates with experience in immunology, particularly lymphocyte cell culture and/or pluripotent stem cell culture. Desirable skills and techniques include 2D and 3D cell culture and bioassays, cell separation, immunostaining, flow cytometry analysis, and molecular biology. | 6/2/2023 |
| 4671 | Advanced Cell Diagnostics Minneapolis, MN Research Associate, Molecular Biology Bachelor’s degree in a science related field. Exp: 0-3 years |
The responsibilities of this position are to assist the Protein Product Development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 6/2/2023 |
| 4672 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in a related field. Exp: up to 2 years |
The responsibilities of this position are to assist the Protein Product Development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 6/2/2023 |
| 4673 | Aerie Pharmaceuticals Fort Worth , TX Associate Scientist Bachelor’s Degree Exp: 1+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As an Associate Scientist you will be trusted to assist with key studies supporting Research & Development for Alcon's surgical, vision care, and pharmaceutical divisions. | 6/2/2023 |
| 4674 | Ajinomoto Bio-Pharma Services San Diego, CA QC Chemistry Associate I Bachelor’s degree in a Life Sciences discipline or equivalent preferred. Exp: zero to two years |
We are currently seeking a QC Chemistry Associate I, an entry level position, individual contributor responsible for conducting routine analysis of raw materials, proteins, peptides and small molecules under general supervision for in-process, release and stability testing. May focus in a specialized area and provide routine analysis and testing according to standard operating procedures in any of the following areas: in process and finished formulations. | 6/2/2023 |
| 4675 | Akouos Boston, MA Associate Scientist, Early Preclinical Development BS in life/health sciences required. Exp: 1 to 3 years |
The Early Preclinical Development team is seeking a highly motivated Associate Scientist to assist in and/or conduct in vivo experiments supporting the development of product candidates from early discovery through IND-enabling stages. The successful candidate has in-depth experience in handling mice, including IP administration of medications, and can follow good documentation practices. The successful candidate will be a reliable, flexible team player who enjoys working in a fast-paced environment and is able to multi-task. | 6/2/2023 |
| 4676 | American Regent Columbus, OH QC Chemist I B.S. in Chemistry, Pharmaceutical Science or related field required. Exp: 1+ years |
As part of a team of Analytical Chemists, this position is responsible for performing the analytical activities necessary to support finished product and raw material groups. | 6/2/2023 |
| 4677 | American Regent Columbus, OH QC Chemist I B.S. in Chemistry, Pharmaceutical Science or related field required. Exp: 1+ years |
As part of a team of Analytical Chemists, this position is responsible for performing the analytical activities necessary to support finished product and raw material groups. | 6/2/2023 |
| 4678 | SteriPharma Syracuse, NY Microbiology Analyst (QA/QC), 3rd Shift, Pharma Bachelor’s degree from a regionally accredited institution in science or related field. Exp: 1-3 years’ |
This position performs environmental monitoring and quality control of aseptic process area, to include testing of finished products, raw materials, and components according to established procedures. Position reviews records for accuracy. Position applies standard concepts, practices, and procedures within the laboratory. Position performs a variety of tasks related to both Quality Assurance and Quality Control. | 5/22/2023 |
| 4679 | Strand Therapeutics Boston, MA Associate Scientist, In Vivo Pharmacology - Immuno-Oncology B.S. or M.S. in Biological Sciences, Bioengineering or related discipline. Exp: 1-3 years |
We are looking for an Associate Scientist to join the Translational Biology group to conduct proof-of-concept, validation, and downstream pharmacology studies to support multiple pre-clinical programs. You will be passionate about scientific discovery, undeterred by bold challenges, and enjoy working as a team to develop the next generation of mRNA medicines. You should be highly organized, a critical thinker, adaptable to changing priorities, and possess a strong ability to collaborate effectively with teams of diverse backgrounds. | 5/22/2023 |
| 4680 | Taconic Biosciences Rensselaer, NY Associate Scientist Molecular Analysis Bachelor's degree in the biological field from a four-year college. Exp: 1-year |
The Associate Scientist Molecular Analysis is responsible for providing support of our genotyping operation, preparing next generation sequencing libraries, and developing new techniques. This person will primarily be responsible for genetic characterization of new rodent models. They are responsible for coordinating between departments to ensure project timelines are met and the appropriate tests are conducted. The role also participates in the development of new assays or techniques when additional analysis is needed. Problem solving is a core part of every day, essential for analyzing new results, and to integrate processes within a high throughput testing lab. | 5/23/2023 |
| 4681 | Taconic Biosciences Rensselaer, NY Senior Laboratory Specialist Molecular Analysis - 2nd Shift Bachelor’s Degree from a four-year college or university. Exp: 1-3 years’ |
The Senior Laboratory Specialist performs a variety of molecular assays on animal samples and must be able to generate high-quality results in a timely manner. This individual should be comfortable working in a high-throughput environment and be able to use proper judgement to make technical decisions on assay performance issues. | 5/23/2023 |
| 4682 | Tenaya Therapeutics South San Francisco, CA Research Associate I/II or Senior Research Associate I B.S. or M.S. in pharmacology, biology, physiology, bioengineering or related discipline. Exp: > 1 year |
Tenaya has an immediate need for a Research Associate I to Senior Research Associate I to support the Pharmacology team. The ideal candidate is a self-starter and problem-solver who will work closely with the team to drive the company’s future success. Ideally, you thrive in a fast-paced environment where every day is unique. You are confident, poised and cool-headed, no matter how much is changing around you. You strive for excellence in every facet of your work, and you understand the excitement and commitment of pharmacology roles. Finally, you love being part of a team aligned around a compelling mission. | 5/24/2023 |
| 4683 | Tessera Therapeutics Somerville, MA Research Associate I/II, LNP Formulation (Contractor) BS/MS in Chemistry, Chemical Engineering, Biomedical Engineering, Material Science, or closely related field. Exp: 0-3 years |
This is a contract position with a July target start date, running through the end of the year (with potential to extend or convert). The Research Associate I/II will be responsible for developing LNP formulations and processes to support the company's in vitro and in vivo pre-clinical studies. We are searching for a driven, enthusiastic, and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 5/26/2023 |
| 4684 | Tessera Therapeutics Somerville, MA Analyst I/II, Quality Control (Contractor) BS/BA degree in biology, chemistry or related field; or MS degree. Exp: BS: 0-2+ years; MS: up to 2 years |
The Quality Control Analyst I/II will be responsible for documentation required for GMP method performance of molecular, plate-based and automated assays. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. The successful candidate will work both independently and as part of a collaborative team to ensure readiness of QC in-process, release and stability test methods used for Tessera drug substances and drug products. This position is a 6-12 month contract role with the possibility of extension/conversion and may leveled up based on years of experience | 5/26/2023 |
| 4685 | Tessera Therapeutics Somerville, MA Research Associate I/II, RNA Production (Contractor) Bachelor's degree or Master's degree in Biochemistry, Molecular Biology, Chemistry, Analytical Chemistry, or related discipline. Understanding of in Exp: BS: 0-4 years ; MS: 0-2 years |
This is a contract position through the end of the year, with a start date of July 11th, 2023 at the earliest. Tessera Therapeutics is seeking a Research Associate I/II for our high-throughput RNA production process. You will support process development for in-vitro transcription, modification, and purification of RNAs to support Tessera's pre-clinical efforts. We seek researchers that are proactive, enthusiastic, and show a passion for process development. The successful candidate should have strong communication and collaboration skills. Strong attention to detail and excellent organizational and documentation skills are highly desirable. | 5/26/2023 |
| 4686 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, RNA Rewriting Bachelor’s or Master’s degree in biology, cell biology, immunology or a related field. Exp: BS/MS: 0-5 years |
The Research Associate/Senior Research Associate will be responsible for building a next generation screening platform, executing screening workflows, and supporting the team with a focus on molecular and cellular biology in the broader context of applying genome engineering technologies. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 5/26/2023 |
| 4687 | TetraGenetics Vancouver, British Columbia, Canada, Ca Research Technician - Sequencing BSc or MSc in Molecular Biology or another relevant field Exp: 1-2 years |
AbCellera is a young, energetic, and rapidly growing tech company with an amazing team that searches, decodes, and analyzes natural immune systems to find antibodies that its partners can develop into drugs to prevent and treat diseases. We are seeking a Research Technician to join our dynamic and multidisciplinary sequencing team. This role is intended for a highly motivated team-player who thrives in a fast-paced work environment with multiple competing priorities, and above all, someone who can learn and grow with us. This is an exciting opportunity to join one of Canada’s most innovative biotech companies and to contribute to our cutting-edge research on antibody engineering, advanced mammalian cell systems, and molecular research supporting the discovery of novel monoclonal antibodies for therapeutic use. | 5/26/2023 |
| 4688 | NeoLight Scottsdale, AZ Biomedical Engineer Bachelor's Degree in Electrical Engineering (Required) from an accredited university or college. Master's degree is preferred. Exp: entry-level |
We seek a full-time entry-level Biomedical Engineer focusing on Electrical Engineering. In this role, you will provide strong, independent technical support to teams that contribute to resolving significant electrical and embedded system issues for the next generation and on-market products. A successful candidate will be a productive individual contributor who works independently with general supervision on larger, moderately complex projects/assignments. In addition, the candidate sets objectives for their job area to meet the objectives of projects and assignments. | 5/26/2023 |
| 4689 | TransMedics Andover, MA Temp-to-Perm Production Test Technician (SECOND SHIFT) BS in Electrical Engineering or equivalent combination of education and experience. Exp: 1+ years |
Responsible for performing testing activities associated with TransMedics’ Organ Care System Hardware and Perfusion Modules. Maintain efforts to ensure all production test related activities are executed in a timely manner to satisfy Company’s Production schedule and quality standards. Assist with maintainance and calibration of equipment used in the testing of electrical components, printed circuit board assemblies and assembled devices per engineering documents and drawings or instructions.Conduct test related activities to support production including but not limited to PCB testing, final system testing, functional testing and burn-in activities. Provide training in testing and inspection methods as required. Maintain individual work area / equipment in a neat orderly manner according to standards including proper disposal of packaging waste, proper storage and use of equipment and parts and management of documentation needed to perform duties. Assist Engineering staff in completion of quality and regulatory activities related to product development, maintenance and/or repair. Assist Test Engineering in the development of new test equipment and protocols. Support Engineering team and Production team efforts to identify opportunities to streamline production through process, test and product design changes. Work with Quality Assurance to maintain an approved internal quality system that meets the requirements of cGMP’s, QSR and ISO requirements. Comply with all work safety rules and regulations. Perform other TransMedics tasks and duties as required. | 5/26/2023 |
| 4690 | Tris Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field. Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. • Carries out responsibilities in accordance with the organization’s policies, SOPs, and state, federal and local laws • Performs testing of raw materials, IP, FP and/or ST samples including dissolution, assay, content/blend uniformity, particle size distribution, and other tests according to the analytical methods, United States Pharmacopeia (USP) procedures in a regulated laboratory environment • Analyzes and interprets test results • Operates general analytical instruments during raw material, IP and FP testing such as High-Pressure Liquid Chromatography (HPLC), Ultra Violet visible spectroscopy (UV/Vis), Automatic Titration, Infra-Red Spectroscopy (IR), Atomic Absorption (AA), Thin Layer Chromatography (TLC) and Dissolution apparatus (distek) • Assists with the identification and troubleshooting of problems with instrumentation and analytical preparations • Meets project deadlines and performance standards as assigned | 5/26/2023 |
| 4691 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate, In Vivo Pharmacology (RA07-7 For RA level: BS ; For Sr. RA level: MS Exp: RA: 0-3+ years; Sr. RA level:0-2+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a motivated researcher to join our In Vivo Pharmacology team as a Research Associate/Senior Research Associate, supporting the preclinical development of our lead therapeutic TCRs. The ideal candidate should have relevant experience in in vivo pharmacology, mechanism of action and anti-tumor efficacy studies, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 5/26/2023 |
| 4692 | Turn Biotechnologies Mountain View, CA Research Associate / Sr. Research Associate - Biology BS/MS in biology, biochemistry, molecular biology, or related discipline. Exp: one year |
Turn Biotechnologies is currently seeking a qualified, highly motivated individual for the position of Sr. Research Associate - Biology. This person will be a highly motivated and responsible individual whose primary purpose is to perform and assist with experiments, analyze data, maintain records, manage projects, maintain lab operations, and other duties as required to meet company goals | 5/26/2023 |
| 4693 | Twist Bioscience Wilsonville, OR Manufacturing Associate Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. | 5/26/2023 |
| 4694 | Twist Bioscience Wilsonville, OR Manufacturing Associate - Gene Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate, Gene Production, will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. | 5/26/2023 |
| 4695 | Twist Bioscience Wilsonville, OR Manufacturing Associate - IgG Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate, Gene Production, will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. | 5/26/2023 |
| 4696 | Twist Bioscience Wilsonville, OR Manufacturing Associate - Reagents Bachelors/ Associates degree in biology, or relevant field is desirable. Exp: 1+ years |
We are looking for motivated and enthusiastic individuals to join our Twist Bioscience Operations Team in Wilsonville, near Portland, Oregon. The ideal candidate will be driven and will do what it takes to keep synthetic biology manufacturing on track in a fast-paced start-up environment. The Manufacturing Associate for the Reagents group will perform reagent handling, basic chemistry and molecular biology protocols in a high-throughput environment. | 5/26/2023 |
| 4697 | Twist Bioscience South San Francisco, CA Research Associate, Biopharma Libraries Bachelor’s or Master’s degree in Molecular Biology, Biochemistry, Chemistry or closely-related field. Exp: 1-3 years |
We are looking for an outstanding Research Associate (RA) to join our CVL team. The Research Associate will support R&D efforts in developing custom DNA-based applications and assays for combinatorial variant library products. The ideal candidate will be driven and willing to learn new techniques. This position will support projects including high-throughput combinatorial library generation, high-throughput cloning processes, custom molecular biology, NGS-based QC, etc. The ideal candidate will be eager to learn, be very organized, have excellent molecular biology/biochemistry knowledge and skills, and communicate effectively with peers/management. | 5/26/2023 |
| 4698 | Twist Bioscience South San Francisco, CA Research Associate, Process Development B.S. in Molecular Biology, Biochemistry, Bioengineering, or a closely-related field. Exp: 1-2 years |
We are looking for an outstanding Research Associate to join our Process Development Team in South San Francisco. If you thrive in a multidisciplinary team environment where every day is different, excel at executing a variety of processes from the lab bench, and are a creative problem solver with a passion for automation and delivering high quality results, we want you to apply! This position supports development of current and future processes for our synthetic Biology product portfolio which will be transferred to manufacturing teams at Twist. | 5/26/2023 |
| 4699 | United Therapeutics Blacksburg, VA Research Associate I/II - Transplant Research Research Associate I/II - Transplant Research Bachelor’s Degree in Arts/Sciences (BA/BS) in Biology, Cell or Molecular Biology, or Biomedical Sciences Exp: RA I: 1+ years |
The Research Associate I/II will record, collect, and analyze experimental data that is obtained during the testing of various artificial organ constructs. The experiments will include bench-top experiments as well as surgical organ transplantations in large animal models. The Research Associate will interact with several collaboration teams and be trained and educated in how to set up and analyze the required experiments. This position will help to efficiently provide analyses and experimental results that will allow to further improve the function and performance of our artificial organs. | 5/26/2023 |
| 4700 | United Therapeutics RTP, NC Research Associate I/II - Cell Isolation Bachelor’s Degree in Arts/Sciences (BA/BS) in biology, cellular and molecular biology, biomedical sciences, biomedical engineering, or biomanufacturin Exp: RA I: 1+ years |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. | 5/26/2023 |
| 4701 | United Therapeutics Manchester, NH Associate Process Engineer/ Process Engineer, Biomaterials Associate Process Engineer: Bachelor’s Degree in Arts/Sciences (BA/BS) in materials science, chemistry, chemical, mechanical or biomedical engineering Exp: APE: 1+ years |
The Associate Process Engineer, Biomaterials (OMG) will be responsible for scaling up and experimenting with large batches of ink to support process and product feasibility goals. This position will also be responsible for periodic quality control (QC) testing. | 5/26/2023 |
| 4702 | Vor Biopharma Cambridge, MA Associate Scientist/Senior Associate Scientist, Discovery & Molecular Engineering Bachelor’s or Master’s degree in molecular biology, biochemistry, genetics, or a related discipline is required. Exp: BS: 0-2+ years’; MS: 1+ years |
Vor Bio is seeking an Associate/Senior Associate Scientist, in the Discovery & Molecular Engineering team. The candidate will contribute towards advancing Vor’s next-generation of genome-engineered hematopoietic stem cells as well as immuno-oncology products using gene editing approaches such as base editing and HDR. The candidate will work in a team environment to execute experimental plans for early discovery research as well as contribute to cell engineering platform development within the Discovery & Molecular Engineering team at Vor. | 5/26/2023 |
| 4703 | Walden Biosciences Cambridge, MA Associate/Research Associate, Cell Systems MS in molecular or cellular biology, or related field. Exp: 0+ years |
As an integral member of our Cell Systems team, the Associate/Research Associate will carry out laboratory research, working collaboratively with the Head of Cell Systems and other members of the Walden Team. This role will contribute to building out the group’s technical capabilities while concurrently undertaking experiments that further our drug discovery programs in vitro and in vivo translational models. | 5/26/2023 |
| 4704 | Zimmer Biomet Warsaw, IN Technician (741378) College/University courses in Microbiology, Biology, Chemistry, Engineering Mechanics, Medical Technology or other related field preferred. Exp: 0 – 3 years |
Responsible for supporting the daily operations of the laboratory at all Zimmer Biomet Warsaw facilities and for operating and maintaining laboratory equipment for the necessary assigned tasks per area work instructions. May also be responsible for ensuring that equipment calibration and maintenance (preventive and/or corrective) is performed. | 5/26/2023 |
| 4705 | Accelerate Diagnostics Tucson, AZ Research Associate, Core Lab Bachelor of Science degree in Microbiology, Molecular Biology, or related life sciences. Exp: 1 year |
The Research Associate is responsible for the routine execution of experiments supporting assay development, technical operations, and core lab. This position can be in different teams including assay development, core lab and technical operations depending upon business needs. | 5/26/2023 |
| 4706 | Accelerate Diagnostics Tucson, AZ Research Associate, Quality Control Bachelor of Science degree in Microbiology, Biochemistry, Molecular Biology, Chemistry, or related life sciences. Exp: 1 year |
The Research Associate for Quality Control is a key member of the Operations Team under the direction of the Team Lead for Consumable Quality Control. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. | 5/26/2023 |
| 4707 | Ambrix La Jolla, CA Research Associate II, Technology MS degree Exp: 0-4 years |
Ambrx is seeking a highly motivated Research Associate to join the Discovery Group. The primary responsibility is to support multiple oncology and immune-oncology projects from discovery to the preclinical phase. The candidate will work in a multidisciplinary and dynamic team environment to help with discovery and develop precision engineered biological drugs that change patients’ lives. | 5/26/2023 |
| 4708 | Genesis Drug Discovery & Development Hamilton Township, NJ Research Associate (In Vivo/Animal Science) Bachelor of Science degree in Life Science required, Master Degree (Preferred) Exp: 1 to 2 years |
We are seeking a highly motivated and talented individual to join our preclinical in vivo oncology and disease associates’ team. The individual will perform in vivo bioassays on mice and rats in a fast-paced, team-oriented collaborative environment. The candidate should have exceptional skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Should have a strong foundation in in vivo oncology & disease models. Excellent communication and computer skills. Attention to detail with organizational and record keeping skills. Motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. Must maintain a professional demeanor and be able to take necessary initiative to meet project timelines and deliverables.We are seeking a highly motivated and talented individual to join our preclinical in vivo oncology and disease associates’ team. The individual will perform in vivo bioassays on mice and rats in a fast-paced, team-oriented collaborative environment. The candidate should have exceptional skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Should have a strong foundation in in vivo oncology & disease models. Excellent communication and computer skills. Attention to detail with organizational and record keeping skills. Motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. Must maintain a professional demeanor and be able to take necessary initiative to meet project timelines and deliverables. | 5/26/2023 |
| 4709 | Genesis Drug Discovery & Development Hamilton; Hamilton Township, NJ Research Associate B.S or M.S. in Molecular Biology, Biochemistry, or a related field. Exp: 1+ years |
Genesis Drug Discovery and Development (GD3), an affiliate of the Genesis Biotechnology Group, is a fully integrated contract research organization providing services to support preclinical drug discovery programs from early discovery through preclinical development. Ingenio Diagnostics, a GD3 company, is seeking a motivated Research Associate to support client-driven molecular biology services in Hamilton, NJ | 5/26/2023 |
| 4710 | Genesis Drug Discovery & Development Hamilton, NJ Research Associate M.S. in Organic or Medicinal Chemistry Exp: 1 year |
VENENUM BIODESIGN LLC is member of Genesis Biotechnology Group located in Hamilton, NJ. We are involved in the discovery of novel small molecule therapeutics for a number of diseases. Venenum has openings for Research Associate Chemists to join our Team. As a member of a multi-disciplinary team you will conduct organic syntheses for one or more research projects, focusing on hit to lead and lead optimization. Additionally, you may be involved in library synthesis, or a collaborative project with a partner company. | 5/26/2023 |
| 4711 | Genesis Drug Discovery & Development Hamilton, NJ Research Associate I Bachelor of Science degree in Life Sciences. Exp: 1 to 2 years |
Invivotek LLC, a member of the Genesis Biotechnology Group, is a Contract Research Organization focusing on phenotypic characterization of genetically modified mice and rats and in vivo pharmacology studies, with the emphasis on immunology, oncology, metabolic and neurodegenerative disease. We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 5/26/2023 |
| 4712 | Katalyst Health Cares and Life Sciences South Plainfield, NJ Quality Analyst Master’s degree in pharmacy, biotechnology, chemistry, biochemistry, chemical engineering, mechanical engineering, industrial engineering, biomedical Exp: 6 months |
Responsibilities : Involve in the design, development, implementation, testing, documentation & support of cGxP systems as per 21 CFR Part 11 & US FDA. Responsible for qualification & validation (IQ/OQ/PQ), master plans, protocols, changes requests, gap & root cause analysis, risk management plans, traceability matrix, summary reports for facilities, equipment, systems & processes. Preparation, review, authorize & submission of documentation for quality compliance & regulatory authorities. | 5/26/2023 |
| 4713 | Paraza Pharma Saint - Laurent, QC, Canada, Ca Associate Scientist – Chemical Sciences MSc in Organic, Bioorganic or Medicinal Chemistry Exp: 1+ years |
The Medicinal Chemistry and Chemical Development groups at Paraza are seeking energetic, results-oriented individuals with proven track records of success to join our dynamic teams. The successful candidate is expected to have experience in modern organic synthesis with good laboratory skills and high productivity. The candidate will be expected to work independently within a team structure, design and execute synthetic routes and troubleshoot when needed. | 5/26/2023 |
| 4714 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 5/26/2023 |
| 4715 | Spriaso Salt Lake City, UT Research Chemists Bachelor's degree in chemistry, chemical engineering, biochemistry, or other related degree concentration. Exp: one year |
These positions entails doing product, process, and analytical functions in support of product and technology development under direction of product development and/or analytical leader. The ideal candidate would possess: • Strong computer, scientific, and organizational skills • Excellent communication (oral and written) and attention to detail • Ability to work independently and as part of a team with internal and external clients, self motivation, adaptability, and a positive attitude • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies | 5/26/2023 |
| 4716 | Vaxess Technologies Cambridge, MA Research Associate / Senior Research Associate, Formulation and Analytical Development Master’s degree in one of the Life Sciences, Chemistry, Pharmaceutical Sciences, Chemical Engineering or Biomedical Engineering. Exp: 0-2+ years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials science, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in formulation and analytical development to join our core team of scientists and engineers. This is a unique opportunity to be part of an emerging early phase clinical company bringing innovative technology to the global market. | 5/26/2023 |
| 4717 | Vaxess Technologies Cambridge, MA Research Associate, Preclinical Studies Master’s degree in one of the Life Sciences. Exp: 0-2+ years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials science, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in translational animal models and wet lab analytical techniques to join our core team of preclinical scientists and engineers. This is a unique opportunity to be part of an emerging early phase clinical company bringing innovative technology to the global market. | 5/26/2023 |
| 4718 | PsychoGenics Paramus , NJ Research Associate - EEG Bachelors degree in the Biological Sciences or related field. Exp: 1-3 years |
We are looking for a highly motivated Researcher for our EEG group. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The candidate must be capable of working both across teams and independently. | 5/16/2023 |
| 4719 | PsychoGenics Paramus , NJ Research Associate 1 – Surgery/Neuroscience Bachelors degree in life sciences, neuroscience, or psychology. Exp: 1+ years |
We are looking for a highly motivated Research Associate in surgery. The successful candidate will work in a team of scientists and researchers supporting the preclinical studies using rodent models and tests. The primary responsibilities of the candidate will include but are not limited to conducting preclinical research using various surgical procedures primarily in the area of pain, animal disease model, and other drug discovery assays as needed. The candidate will be responsible for surgeries, tissue collection and drug administration, proper execution of experiments, and preliminary data analysis. The candidate must be capable of working across teams and independently. | 5/16/2023 |
| 4720 | PsychoGenics Paramus , NJ Research Associate - Neuropharmacology Bachelors or Masters Degree in the biological sciences, neuroscience, or related field. Exp: 1-3 years |
We are looking for a highly motivated Research Associate in neurodegenerative disorders. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The primary responsibilities of the candidate will include, but are not limited to, dosing animals, conducting behavioral assessments for neurodegenerative disorders, and dissection and tissue collection. The candidate will be responsible for coordinating studies and the proper execution of experiments. The candidate must be capable of working both across teams and independently. | 5/16/2023 |
| 4721 | Proteintech Rosemont, IL Scientist I, Bioconjugation Bachelor’s degree in an appropriate area of specialization (Molecular Biology, Cell Biology, Biochemistry, or related life sciences). Exp: 1+ years |
New grads with lab experience are encouraged to apply. The successful candidate will support the development and optimization of processes in bioconjugation of antibodies for use in various applications like Flow Cytometry and IHC. | 5/16/2023 |
| 4722 | Quansys Biosciences West Logan, UT Formulation Specialist I-II Bachelor’s degree in Biology, Chemistry, Biotechnology, or related field is required. Exp: 1-3 years |
A Formulation Specialist I-II is responsible for meeting production schedules in a fast-paced, high throughput laboratory setting. This is not a production line job. Duties may include the production of immunoassay components, chemical buffers, biological diluents/reagents, coated plates, and/or assembled kits, for customer order fulfillment.They will be responsible, under minimal supervision, to follow established SOPs in order to support the goals of the department. They will be expected to assist in troubleshooting problems and keeping SOPs up to date. Some degree of professional latitude, creativity, and self-management is expected. This position may manage very specific aspects of the manufacturing process within the department. Typically, they will be expected to master at least two aspects of the production process. | 5/17/2023 |
| 4723 | Quansys Biosciences West Logan, UT Quality Control Associate I Bachelor’s degree in Biochemistry, Microbiology, or Chemistry or related field is required. Exp: 0-1 years |
A Quality Control Associate I is responsible for maintaining a high level of quality and customer satisfaction while meeting production schedules in a fast-paced, high throughput industrial setting. Associate will be responsible for the quality control of many product types including chemical buffers, biological diluents/reagents, coated plates, and/or assembled kits, for customer order fulfillment. They will be responsible, under minimal supervision, to follow established SOPs to support the goals of the department. They will be expected to assist in troubleshooting problems and keeping SOPs up to date. Some degree of professional latitude, creativity, and self-management is expected. This position may manage very specific aspects of the QC process within the department. | 5/17/2023 |
| 4724 | Quanterix Billerica, MA Research Associate BS in Chemistry, Biochemistry, Engineering, or Life Science Exp: 0+ years |
We are seeking a well-rounded and highly motivated Research Associate who thrives in a problem-solving oriented position to join our Assay Technical Support team. Key responsibilities will include (1) problem solving escalated issues from manufacturing and quality control, (2) making process improvements identified during investigations, and (3) work as part of the ATS team to drive continuous improvement of the customer experience with Quanterix assays. | 5/17/2023 |
| 4725 | Quanterix Billerica, MA Associate Process Engineer Bachelor’s Degree in Chemistry/Biochemistry/Biology/related field; or Scientific Associate Degree with additional years of relevant experience. Exp: 1+ years |
We are looking for an experienced and motivated Associate Process Engineer in Billerica, MA to join our Pilot Plant team. This position will be responsible for a variety of activities including production of small scale reagents, continuous improvement of existing processes, and establishing manufacturing procedures/work instructions in support of new product in accordance with cGMP. | 5/17/2023 |
| 4726 | Quanterix Billerica, MA Associate Process Engineer Bachelor’s Degree in Chemistry/Biochemistry/Biology/related field; or Scientific Associate Degree with additional years of relevant experience. Exp: 1+ years |
We are looking for an experienced and motivated Associate Process Engineer in Billerica, MA to join our Product Transfer team. This individual will be responsible for a variety of activities including production of small scale reagents, continuous improvement of existing processes, and establishing manufacturing procedures/work instructions in support of new product in accordance with cGMP. | 5/17/2023 |
| 4727 | Quanterix Billerica, MA Research Associate, Product Validation B.S. degree in biological or physical sciences required Exp: 1-3 years |
We are looking for a motivated candidate to join our System Development team. This individual will report to the Associate Director of System Development to provide technical support in Validation testing across Quanterix biomarker systems. This position requires the candidate to collaborate cross-functionally to understand user requirements and implementation details of system changes to support the execution of immunoassay-based test methods that demonstrate continuity of assay performance on the system. The individual will be responsible for reviewing test plans, executing those plans, and documenting test results. To support this, this role will require the candidate to assist in the detailed analysis of assay and equipment performance for both new systems and upgrades to existing systems, inclusive of both hardware and software changes. | 5/17/2023 |
| 4728 | Quidel Carlsbad, CA Associate Process Group Chemist B.S./B.A. Life/Applied Sciences or equivalent experience. Exp: 6 months |
As we continue to grow as QuidelOrtho, we are seeking an Associate Process Group Chemist, in accordance with forecasted requirements, participates in the manufacture of products within QSR and ISO regulations. This position reviews and reconciles documents and work orders, supports assigned projects with supervision, participates in product transfers, supports departmental troubleshooting and process improvement teams, and displays an improving working knowledge of business processes as they relate to manufacturing. This role is located in Carlsbad, CA onsite. | 5/17/2023 |
| 4729 | Quidel Athens, OH Clinical Repository Associate BA/BS in life sciences, similar field or equivalent. Exp: 1+ years |
As we continue to grow as QuidelOrtho, we are seeking a Clinical Biorepository Associate to oversee a system to maintain and coordinate the inventory and processing of biorepository samples and research materials to support clinical operations and new product development. The Clinical Biorepository Associate will receive samples and maintain physical biospecimen freezer inventories. They will work collaboratively with Clinical Operations management and interface with external biorepositories and 3rd party bio-specimen brokers for specimen procurement, as well as clinical collection sites. This is an onsite position in Athens, OH. | 5/17/2023 |
| 4730 | Quidel San Diego, CA Assay Verification and Validation Technician Bachelor’s degree in Biology, Chemistry, Molecular Biology, Biochemistry, or related discipline. Exp: 1-2 years |
As we continue to grow as QuidelOrtho, we are seeking an Assay Verification and Validation (V&V) Technician to be responsible for verification and validation testing of new products and changes to released products. The Assay V&V Technician contributes to verification and validation activities for multiple systems comprised of assays, reagents, consumables, instruments, and software. The role requires a strong detail-focused skill set to execute tests of products exiting development and to further support and improve products within manufacturing. This is an onsite position in San Diego, CA. | 5/17/2023 |
| 4731 | Quidel San Diego, CA Production Chemist Master’s degree in Chemistry, Biological Sciences, or equivalent. Exp: 0-2 years |
As we continue to grow as QuidelOrtho, we are seeking a Production Chemist. Under minimal ongoing supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP under the direction of senior staff including manufacturing products within QSR and ISO regulations. This position will be located onsite in San Diego, CA | 5/18/2023 |
| 4732 | Quidel San Diego, CA Production Chemist Master’s degree in Chemistry, Biological Sciences, or equivalent. Exp: 0-2 years |
As we continue to grow as QuidelOrtho, we are seeking a Production Chemist. Under minimal ongoing supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP under the direction of senior staff including manufacturing products within QSR and ISO regulations. This position will be located onsite in San Diego, CA | 5/18/2023 |
| 4733 | Quidel San Diego, CA Production Chemist Master’s degree in Chemistry, Biological Sciences, or equivalent. Exp: 0-2 years |
As we continue to grow as QuidelOrtho, we are seeking a Production Chemist. Under minimal ongoing supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP under the direction of senior staff including manufacturing products within QSR and ISO regulations. This position will be located onsite in San Diego, CA | 5/18/2023 |
| 4734 | Rani Therapeutics San Jose, CA MECHANICAL ENGINEER Bachelor’s Degree in Mechanical Engineering; or Master’s degree in Mechanical Engineering or equivalent. Exp: BS: 1-3 years |
We are seeking an exceptional Mechanical Engineer to design and develop semi or fully automated equipment that are used for high volume, disposable devices. Your role is to find creative and sound engineering solutions to challenging problems with strong focus on quality, reliability and execution. This is a hands-on position that requires interaction and collaboration with a cross-functional team including Engineering, Manufacturing, Biology, Quality, Facilities and Sustaining. | 5/18/2023 |
| 4735 | Reaction Biology Malvern, PA Research Associate - Biochemical Assays Bachelor’s or master’s degree in biochemistry or related discipline. Exp: 0-2 years |
We are currently seeking a Research Associate for our Malvern, PA facility. We are looking for a reliable and motivated individual with a strong science background to work in our lab. The position is an onsite entry-level bench position with the primary duty of executing a variety of enzymatic assays. | 5/18/2023 |
| 4736 | Recursion Pharmaceuticals Salt Lake City, UT Research Associate, In Vitro (iPSC) Bachelor's or Master's degree in cell biology or related field Exp: 1+ years |
Reporting to our Director, In Vitro, you'll join our newly formed team focused on the utilization of human pluripotent stem cells (hPSCs) to model neurodegenerative diseases. You will be joining a fast-paced team of multi-disciplinary scientists who are focused on bringing new therapeutics to patients at an accelerated pace. This team helps Recursion develop, refine, and characterize state-of-the-art differentiation technology and advanced disease models at a large scale for one of the world’s leading companies in AI-guided drug discovery. This high performing team is bold, creative, and has a team-first mindset alongside a deep passion for exploring the unknowns in neuroscience. | 5/18/2023 |
| 4737 | Minaris Regenerative Medicine Allendale, NJ QA Associate II BS or higher education degree in a scientifically related field. Exp: 1 -3 years |
The Quality Assurance Associate is responsible for performing Quality Assurance activities under direct supervision of daily tasks in support of Quality Systems and/or client procedures including but not limited to document management, review of QC data, material releases and final product releases as well as assisting Quality management with department needs. | 5/19/2023 |
| 4738 | Minaris Regenerative Medicine Allendale, NJ QC Microbiology Analyst I Bachelor's degree in a science or relevant field required. Exp: 0-2 years |
This position will report into the Supervisor of QC Microbiology. The Quality Control Microbiology Analyst I serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. | 5/19/2023 |
| 4739 | R & D Systems Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 5/19/2023 |
| 4740 | R & D Systems Minneapolis, MN Research Associate, Molecular Biology Bachelor’s degree in a science related field Exp: 0-3 years |
The responsibilities of this position are to assist the Protein Product Development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 5/19/2023 |
| 4741 | R & D Systems Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in a related field Exp: up to 2 years |
The responsibilities of this position are to assist the Protein Product Development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 5/19/2023 |
| 4742 | R & D Systems Minneapolis, MN Advanced Research Associate, Antibody Development Master’s degree in a science related field Exp: 1-2 years |
As an Advanced Research Associate within the Antibody Development Business Unit, you’ll work with and support the mouse hybridoma group at the Minneapolis site which is a critical resource used by various business units - Antibody Development, Protein Development, Immunoassays, QC and Stem cell groups. | 5/19/2023 |
| 4743 | R & D Systems Minneapolis, MN Research Associate, Antibody Development Bachelor’s degree in a scientific discipline or equivalent Exp: 0-2 years |
Key Responsibilities: Mammalian cell culture, including antibody-producing hybridoma cultures. Responsible for rodent immunization and hybridoma fusion Large-scale antibody screening assays. Protein analysis using SDS-PAGE, Western Blot, and ELISA Written and electronic record-keeping of experimentation Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance with the job. Performs additional duties as assigned. | 5/19/2023 |
| 4744 | Roche Carlsbad, CA Research Associate I/II - Assay Development Research Associate I: B.S. in Biochemistry, Molecular Biology, Analytical Chemistry or a related field; Exp: RAI: 0 - 3 years |
Please consider the location of this job will be La Jolla / Torrey Pines. The Research Associate I/II will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision. You will investigate, adapt or modify experimental methods and technologies for project advancement. This is a unique opportunity to leverage your background and skills in molecular diagnostics to enhance and build your career by working cross-functionally. An exciting career opportunity where your contributions will impact business opportunities through successful completion of projects. | 5/19/2023 |
| 4745 | SAMDI Tech Chicago, IL Research Assistant B.S in biology, biochemistry, chemistry, or related field Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. | 5/19/2023 |
| 4746 | Sarepta Therapeutics Andover, MA Gene Therapy Potency Associate B.S. degree in molecular biology or cell biology Exp: 0 – 2 years |
This individual will support quality control laboratory activities conducted at the Sarepta Andover facility in the field of AAV therapeutic release and stability. The individual will assist in conducting GMP QC release and stability testing using state of art In vitro Potency Assay. The candidate should have hands-on experience in SDS-PAGE, Western blotting, enzyme activity measurements, protein extraction, and quantification methods. The position requires a background in cell culture, tissue lysate sample preparation, protein analysis, and performing assays in a BSL-2 environment. The individual may work under the direction of a subject matter expert conducting experiments and supporting analytical method validation and qualification activities. All aspects of this position involve working in a GMP-compliant manner. This position requires occasional coverage late evening and a few hours on weekends. | 5/19/2023 |
| 4747 | Scanogen Baltimore, MD CHEMICAL AND BIOMOLECULAR ENGINEER Chemical Engineering degree Exp: 1+ years |
Scanogen is looking for a motivated and skilled engineer to join our R&D team. We are a rapidly-growing start-up company developing a nucleic acid detection platform that will change how diseases are diagnosed. We need highly driven and inventive individuals. The main focus is to optimize and automate biomolecule detection assays. | 5/19/2023 |
| 4748 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science. Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 5/19/2023 |
| 4749 | SeaGen Bothell, WA Research Associate B.S. in Chemistry, Biochemistry, or related discipline. Exp: 0-2 years |
Seagen is seeking a Research Associate to participate in the development of drug programs. Responsibilities: Conduct experiments, analyze data and report results to relevant parties to support manufacturing process development. Requirements: BS or MS in chemistry, biochemistry, biological sciences, or a related discipline. Fundamental knowledge of protein chemistry and knowledge related to the detection of protein posttranslational modifications and chemical degradations using bioanalytical techniques. Hands-on analytical experience with liquid chromatography, electrophoretic and other analytical methods (e.g., SEC, RP, CEX, CE-SDS, cIEF). Strong organization and time management skills with attention to detail. Strong desire to achieve team and individual goals in a collaborative team environment. | 5/19/2023 |
| 4750 | SeaGen Bothell, WA Research Associate I Degree in chemistry, biochemistry, chemical engineering or related field, B.S. Exp: 0-2 years' |
The Conjugation Process Development group is seeking a Research Associate I to assist in the development of conjugation processes for antibody-drug conjugates (ADCs). The Research Associate I executes experiments under the direction of others or independently handles those that are routine in nature with minimal variation in design and execution. They compile data in electronic laboratory notebooks and create informative tables and graphs. They occasionally present at group or department meetings. | 5/19/2023 |
| 4751 | SeaGen Bothell, WA Research Associate II M.S. Exp: 0-2 years |
The Research Associate II independently performs standardized experiments with minimal variation in design and execution. They plan and execute more complex experiments under the direction of others. They compile data in electronic laboratory notebooks, create summaries, and analyze data. They occasionally present at group or department meetings. They collaborate cross-functionally and use scientific literature to support experimental work. | 5/19/2023 |
| 4752 | SeaGen Bothell, WA Research Associate II - Pharmacokinetics M.S. Degree in relevant scientific discipline such as: Molecular Biology, Cell Biology, or Biochemistry. Exp: 0-2 years |
The Translational ADME and PKPD (TAPP) group at Seagen is committed to the development of safe and effective therapeutics by characterizing the absorption, distribution, metabolism, elimination and pharmacokinetic-pharmacodynamic relationships of drug candidates in nonclinical species. TAPP collaborates with colleagues across Seagen (early discovery, toxicology, clinical pharmacology, regulatory, etc.) to inform lead selection, conduct nonclinical development studies, and contribute to regulatory filings. The TAPP group is seeking a highly motivated Research Associate to support nonclinical development of large molecule drug candidates. The responsibilities of this role include management of samples, reagents, and mammalian cell cultures as well as execution of cell-based assays. | 5/19/2023 |
| 4753 | SeaGen Bothell, WA Research Associate II, Potency Assays M.S. in Biological Sciences or a related discipline. Exp: 0-2 years |
We are seeking a highly organized and motivated research associate II to join our Potency Assay Development team. The potency team is responsible for the development, qualification, and implementation of cell-based assays, binding assays, and other methods to support lot release and stability testing and the biological characterization of therapeutics in the Seagen pipeline. The ideal candidate for this RAII position should be proficient in cell-based assay development experience, ELISA assay development, cell culture, and cell bank generation. Working experience in potency assays, cytotoxicity assays, live-cell imaging, and flow cytometry is highly desirable. | 5/19/2023 |
| 4754 | SeaGen Bothell, WA Research Associate II, Pharmaceutical Sciences M.S. Degree in Pharmaceutical Sciences, Biochemistry, Biological Sciences, Chemical Engineering, or related discipline. Exp: 0-2 years' |
The Research Associate II independently performs experiments that are routine in nature with minimal variation in design and execution. This role will plan and execute more complex experiments under the direction of others. The Research Associate II compiles data in electronic laboratory notebooks, creates summaries, and analyzes data. This role will occasionally present at group or department meetings. This position collaborates cross functionally and uses scientific literature to support experimental work. | 5/19/2023 |
| 4755 | Seran Bioscience Bend, OR Engineer I Bachelor or Master’s degree in chemical engineering, pharmaceutics, chemistry, bioengineering, mechanical engineering, materials science, physics, or Exp: entry-level |
Serán seeks to hire an entry-level Engineer to contribute in an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. The role requires strong hands-on laboratory skills and the ability to apply fundamental scientific principles to solve problems. Strengths in data collection, analysis, proactive communication, and continuous learning by textbooks, journals, and training will enable the successful candidate to thrive. Candidates should possess a bachelor’s or master’s degree in chemistry, chemical engineering, biology, biological engineering, mechanical engineering, materials science and engineering, or physics. Demonstrated research experience is desirable. Candidates with additional relevant experience are also invited to apply. | 5/19/2023 |
| 4756 | Sestina Bio Pleasanton, CA Research Assistant/Research Associate I, Synbio Bachelor’s degree in a scientific discipline or associate degree from a laboratory science or biotechnology program will be considered. Exp: 1+ year |
The Research Assistant/Research Associate I will primarily assist in lab management services such as media preparation, inventory, and shipping & receiving activities. They will report directly to the Laboratory Manager but will have opportunities to cross train and support other groups such as Screening, Analytic Chemistry, and Strain Banking. The successful candidate will be a team player who works within the group to meet department goals, objectives, and tasks to achieve desired results. They can respond to new requests with appropriate urgency and an organized approach and hold themselves accountable to fulfill assigned tasks and achieve results within assigned timelines. | 5/19/2023 |
| 4757 | Smithers Wareham, MA Associate Chemist I - Chemistry - Smithers B.S. degree in chemistry or related field. Exp: 6 months |
Smithers Environmental Risk Sciences division is seeking an Associate Chemist in the Chemistry Department at our Wareham, MA location. Position is expected to perform varied and often complex and difficult procedures somewhat independently. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Operates and may maintain, under supervision, test equipment and apparatus of moderate complexity. May provide information for initial data interpretation and test system conformance to expectations. Records, compiles and reduces laboratory data in real time in a complete and thorough manner for individual assignments. May produce reports. | 5/19/2023 |
| 4758 | Pacira Biosciences San Diego, CA QA Associate 1 BS/BA degree in scientific discipline. Exp: 1 year |
This person is to assist and support the organization with GMP compliance, monitoring conformance to established quality assurance processes and GMP standards for manufacturing. | 5/8/2023 |
| 4759 | Pacira Biosciences San Diego, CA QC Analyst 1 BS degree in Chemistry. Exp: 1 year |
The purpose of this position is to carry out assigned laboratory duties which may include sampling, testing, and evaluating analytical data on samples such as raw materials, in-process and final products. | 5/8/2023 |
| 4760 | Pall Danvers, MA Research Associate BSc or BA in a Scientific discipline. Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure. | 5/8/2023 |
| 4761 | Par Pharmaceutical Rochester, MI Quality Associate Specialist, Product Release (Day Shift) BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 5/8/2023 |
| 4762 | Par Pharmaceutical Rochester, MI Chemist I (Afternoon Shift) Bachelor of Science Degree in chemistry, chemical engineering or related field with analytical chemistry coursework required. Exp: 1+ years |
The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. May participate in investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. | 5/8/2023 |
| 4763 | Par Pharmaceutical Rochester, MI Quality Associate Specialist, Product Release - Midnight Shift BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 5/8/2023 |
| 4764 | Par Pharmaceutical Horsham, PA QC Analyst II – Microbiology M.S. in a Biological Science or related field. Exp: 1-3 years’ |
The QC Analyst II – Microbiology will perform microbiological testing, release of in-process, intermediates and finished products, and testing for validation purposes. This role is responsible for authoring new SOPs and/or revising of existing documentation. Additionally, this role is responsible for writing Deviation Investigations, Laboratory Assessments, and Investigation Reports. | 5/8/2023 |
| 4765 | PreProTech Middleton, WI Associate Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4766 | PreProTech Middleton, WI Associate Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4767 | PreProTech Middleton, WI Associate Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4768 | PreProTech North Chicago, IL Associate Scientist - Sample Management Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Possesses a thorough understanding of sample management processes and works closely with scientists and project managers to ensure samples are received and transferred in accordance with SOPs and study protocols. Develops independence in performing routine work and ability to organize, manage and set priorities for multiple tasks. Demonstrate the ability to document according to ALCOA documentation practices, communicate observations and escalate issues effectively. | 5/10/2023 |
| 4769 | PreProTech Boston, MA Associate Scientist - Analytical Development Bachelor's degree degree in Chemistry, Biochemistry, Chemical Engineering or Pharmaceutical Chemistry. Exp: 0-2 years |
As an Associate Scientist, you will use state-of-the-art technologies to perform traditional and innovative analytical techniques and Quality-by-Design principles to develop and validate the analytical tools used to ensure the safety, efficacy, and quality of the customer pharmaceutical products. As a member of the Analytical Development team, you will provide project support to the drug development programs at the customer site through laboratory techniques commonly used in the analysis of pharmaceuticals such as HPLC,UPLC and Dissolution | 5/10/2023 |
| 4770 | PreProTech Cambridge, MA Associate II, Manufacturing (nights) Bachelor's Degree in STEM or Biotech related Certificate Exp: 1-2 years |
The Formulation Technician II is an associate with a moderate to advanced level of technical expertise and experience. They may independently perform routine operations commensurate with their experience and training. | 5/10/2023 |
| 4771 | Personalis Menlo Park, CA Clinical Lab Associate 1 - Temp (6 months) BA/BS in a biological discipline. Exp: 0-2+ years |
This position is currently in Menlo Park and will be moving to Fremont, You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. | 5/10/2023 |
| 4772 | Personalis Fremont, CA Senior Research Associate, Process Development M.S. Exp: 1-3 years |
The Senior Research Associate within the Process/Product Development group will support the assay development and documentation for new or existing NGS-based products in a regulated environment (FDA-QSR, CLIA, CAP, ISO regulations). This role requires a broad knowledge of molecular biology and assay development techniques. | 5/10/2023 |
| 4773 | Pharmaron Exton, PA Associate Scientist - Permeability Bachelor of Science. Exp: 0-2-year |
Pharmaron (Exton) Lab Services LLC is seeking a candidate to join the Drug Transporter & Cell Manufacturing team to prepare assay solutions, perform cell-based permeability assays, conduct studies, and perform other lab duties. | 5/10/2023 |
| 4774 | Pharmaron Exton, PA Associate Scientist - Permeability Bachelor of Science. Exp: 0-2-year |
Pharmaron Lab Services LLC is seeking a candidate to join the Drug Transporter & Cell Manufacturing team to prepare assay solutions, perform cell-based permeability assays, conduct studies and perform other lab duties. | 5/10/2023 |
| 4775 | Pharmaron Germantown, MD Laboratory Technician Bachelor's degree in related field Exp: 6 months to 1 year |
Come Join Our Growing Team! We are looking for motivated individuals to join our laboratory in Germantown, MD. This is an opportunity for recent graduates to make a real impact in a highly scientific and regulated environment, demonstrate leadership, ambition and the desire to grow with the department. | 5/10/2023 |
| 4776 | Phitonex Middleton, WI Entry Level Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4777 | Phitonex Richmond, VA Assistant/Associate Scientist Bachelor's degree in Chemistry, Biochemistry, or equivalent and relevant formal academic / vocational qualification. Exp: Assistant Scientist: 0 to 1 year; Associate Scientist: 1+ years. |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4778 | Phitonex Worcester, MA Associate Scientist - Separations and Automation Technologies Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0-2 years |
In this position as an Associate Scientist, you should possess a thorough understanding of laboratory procedures. You will perform a variety of complex sample preparation and analysis procedures to quantitatively measure biopharmaceutical compounds in a variety of biological matrices. Instrumentation is primarily HPLC, CE, and LC/MS. Hamilton Liquid Handlers Protein Maker affinity purification is used as well. Requires following analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against acceptance criteria, methodology, protocol and product specifications. Enters data into databases and reports. | 5/10/2023 |
| 4779 | Phitonex St Louis, MO Cell Culture Technician II (Day Shift) Bachelor’s degree in Biology, Biochemistry or Chemistry seen as a plus. Exp: 1-3 years |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. They will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 5/10/2023 |
| 4780 | Phitonex Florence, SC Analytical R&D Scientist I Bachelor’s degree in chemistry or related field required. Exp: 1-2 years |
The Scientist I conducts laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Utilizes judgment in making adaptation and modifications on all assignments. Provides routine analyses in an analytical chemistry laboratory following standard practices. Performs analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results | 5/10/2023 |
| 4781 | Plex Pharma San Diego, CA Research Associate, Biology & Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field. Exp: 1-3 years |
Plex Pharmaceuticals (www.plexpharma.com), a biotechnology company with a focus on developing novel drugs targeting misfolded and aggregated proteins, has an immediate opening for a Research Associate. The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 5/11/2023 |
| 4782 | PPD Cranbury, NJ Scientist I - Protein Production Minimum Bachelor of Science (B.S.) in chemistry or related field Exp: 1+ years |
The Research Scientist I role is responsible for helping to develop recombinant cytokine products for the life-science research market. This role will report to our Director, Lab Operations. Day-shift Opportunity. | 5/11/2023 |
| 4783 | PPD High Point, NC R&D/Manufacturing Scientist II Bachelor’s degree in Pharmaceutical Science, Nanoscience, Chemistry, or related field of study. Exp: 1 year |
Lead technical/scientific project activities applying expertise and experience in the development of appropriate execution strategies and technical solutions to meet client expectations. Lead or participate in technical discussions with client. Engage in the management of clients, processes and equipment design for clinical, scale up and registration batches including tech transfer of projects to and from clients. Lead the design and evaluation of formulations and manufacturing processes and support problem solving as necessary. Manage resources in the function to achieve project and team objectives and coach people in their work group in areas such as the drug development process and DDMT systems. Liaise with Project Management, Facility/Equipment Schedulers, Materials Management, Analytical Development and other functional areas to meet project and team objectives. | 5/11/2023 |
| 4784 | PPD Plainville, MA Scientist I, Upstream Process Development (Viral Vector Services) Bachelor’s Degree in biology, chemistry, biochemistry, (bio)chemical engineering, biomedical engineering, or a related field. Exp: 1+ years’ |
As a member of the Upstream Process Development team, you will have the opportunity to learn to operate cutting-edge instruments and perform activities spanning the full cell line and cell culture production process. This is a hands-on bench scientist position. The ideal candidate shall have excellent lab skills, strong documentation skills, demonstrated ability to analyze and interpret data to draw conclusions and make recommendations, and strong collaboration and teamwork skills. As a member of the Process Development team, you will work with project leads to support the successful execution of experiments and technical transfer activities. This will include supporting the technical transfer process assessments, Pilot Plant activities and transfer into cGMP manufacturing. This will also include late-phase process characterization of viral vector manufacturing processes. | 5/11/2023 |
| 4785 | PPD Lexington, MA Process Engineer I Bachelor’s degree in Mechanical, Chemical, Biochemical/Biomedical, Electrical, or Automation Engineering, or related field of study. Exp: 1 year |
Support the manufacturing operations team to optimize overall equipment efficiency. Support the procurement of new systems, oversee FATs, SATs and Qualification of these new systems, layout configuration for new clients, and PFD development and equipment readiness for tech transfers. Execute process equipment improvement projects stemming from process changes/optimizations, CAPAs, and new capacity demands including compliance item. Drive continuous improvement and operational excellence culture through self-detecting and self-correcting processes and systems and instilling strong ownership and accountability. Ensure high levels of communication with team, support resources, and management regarding issues and resolutions. | 5/12/2023 |
| 4786 | ProteinSimple Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 5/12/2023 |
| 4787 | ProteinSimple San Marcos, CA Chemistry Associate Bachelor’s degree in a related field. Exp: up to 3 years |
This position is responsible for the developing and or formulation of controls, calibrators, working solutions, and intermediates in the production and development of Bio-Techne's various product lines. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 5/12/2023 |
| 4788 | ProteinSimple San Marcos, CA Chemistry Associate Bachelor’s degree in a related field. Exp: up to 3 years |
This position is responsible for the developing and or formulation of controls, calibrators, working solutions, and intermediates in the production and development of Bio-Techne's various product lines. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 5/12/2023 |
| 4789 | ProteinSimple Minneapolis, MN Quality Technician Position requires an MLT/MLS degree, Bachelor’s degree in Biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. Other tasks include proofing labels and assay sheets. This position will adhere to safety regulations. Perform additional duties as assigned. | 5/12/2023 |
| 4790 | ProteinSimple Minneapolis, MN Advanced Research Associate, Antibody Development Master’s degree in a science related field. Exp: 1-2 years |
As an Advanced Research Associate within the Antibody Development Business Unit, you’ll work with and support the mouse hybridoma group at the Minneapolis site which is a critical resource used by various business units - Antibody Development, Protein Development, Immunoassays, QC and Stem cell groups. | 5/12/2023 |
| 4791 | ProteinSimple Minneapolis, MN Research Associate, Antibody Development Bachelor’s degree in a scientific discipline. Exp: 0-2 years |
Mammalian cell culture, including antibody-producing hybridoma cultures. Responsible for rodent immunization and hybridoma fusion Large-scale antibody screening assays. Protein analysis using SDS-PAGE, Western Blot, and ELISA Written and electronic record-keeping of experimentation Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance with the job. Performs additional duties as assigned. | 5/12/2023 |
| 4792 | Protomer Technologies San Diego, CA Sr. Protein Chemist Master’s Degree in biochemical sciences. Exp: 0-3 years |
We are seeking a highly motivated senior associate scientist with experience in protein purification and characterization to join the Protein Biosciences Group. The successful candidate will have in depth understanding and hands-on experiences in protein purification, and broad knowledge and experience in related fields such as protein expression, analytical and biophysical characterization of proteins. | 5/12/2023 |
| 4793 | Protomer Technologies Pasadena, CA Chemist / Biochemist Undergraduate degree in chemistry, biochemistry, chemical engineering with working knowledge of standard biochemistry or chemistry lab techniques. Exp: 0-3 years |
The ideal candidate will have a bachelor’s or master’s degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a team player in a fast-paced research setting. The applicant will be responsible for assisting Protomer’s senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively participate and present in team meetings and is expected to contribute to the team’s progress and success. | 5/12/2023 |
| 4794 | Protomer Technologies San Diego, CA Biologist - In Vitro B.S. in biology, molecular and cellular immunology or a related biological area; Or M.S. in biology, molecular and cellular immunology or a related bi Exp: B.S.: 1-3 years; M.S.: 0-2 years |
The successful biologist will report to a PhD senior scientist in the group located at Lilly in San Diego, CA. You will work in a highly team-oriented and collaborative setting. Working independently to design, develop and validate immunology cell-based functional assays with the goal to deliver preclinical data to support novel therapeutics for future clinical testing will be expected. As a biologist, you will also investigate the mechanism of action of biological and small molecule therapeutics. | 5/12/2023 |
| 4795 | Protomer Technologies San Diego, CA Biologist B.S or M.S in Biological Sciences (Molecular Biology, Protein Biochemistry, Cell Biology) Exp: 0 - 5 Years |
We are looking for a research associate to join our Biotherapeutic Discovery and Research team, with a goal to further our efforts in the discovery and optimization of novel antibodies for therapeutic applications. The successful candidate should possess solid molecular biology, microbiology and laboratory skills and apply theoretical, technical and - if possible - hands-on expertise in protein display/discovery and engineering technologies to help evaluate, optimize and identify lead antibody molecules for clinical development. | 5/12/2023 |
| 4796 | Protomer Technologies San Diego, CA Biologist - Antibody Discovery B.Sc. in Biological Sciences (Biochemistry, Molecular/Cell Biology, Biotechnology or related field) Exp: 1+ years |
We are looking for a highly motivated Biologist with a diversified background in both in vitro biology and biochemical assay development to join our Antibody Discovery group in Biotechnology Discovery Research. The successful candidate will have a strong research background in biochemical and cell-based assays, or other relevant evaluation methods. The successful candidate will join a highly interactive, collaborative, and innovative scientific team to discover and advance large molecule drugs to combat diseases in the diabetes, pain, neurodegenerative and auto-immune areas. The candidate will collaborate with a multidisciplinary team to support the development of therapeutic antibodies and advance technology. | 5/12/2023 |
| 4797 | Protomer Technologies Indianapolis, IN In Vivo Biologist Undergraduate degree in biology/animal science/veterinary technology or a closely related field. Exp: 1-2 years |
The Lilly Diabetes Obesity and Complications Therapeutic Area (DOCTA) is focused on discovery and development of new therapeutics for the treatment of medical complications arising from type 2 diabetes. The cardiorenal team is seeking a highly skilled and motivated biologist to join the discovery research team. This role will craft experiments using animal models of cardiorenal and cardiometabolic diseases. We need a task-oriented and self-motivated biologist who can perform detailed research studies with minimal direction. This will be an opportunity to work cross-functionally within Lilly Research Laboratories and with external collaborators. If you have actively participated in heart failure drug hunting teams and served as a scientific and technical advisor to project teams, we would love for you to apply? Join the Lilly team today! | 5/12/2023 |
| 4798 | Molecular Devices Danvers, MA Research Associate BSc or BA in a Scientific discipline. Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure | 5/3/2023 |
| 4799 | Molecular Devices Coralville, IA Research Scientist II-Enzyme Development Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field). Exp: one or more years |
The Research Scientist II, under minimal direction, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with the development and characterization of new IDT protein products in the CRISPR, qPCR, and NGS domains. This position is responsible for planning and executing experiments, analyzing data, and reporting/presenting findings as well as supporting IDT customers. A background in bacterial genetics and/or protein engineering is highly preferred. This position is equivalent to a Research Assistant II position at an academic institution. | 5/3/2023 |
| 4800 | Molecular Devices Bellevue, WA Electrical Engineer - Sea-Bird Scientific (Hybrid) Entry-Level: MS Exp: 1 years |
We need an engaged, talented Electrical Engineer to join our Product Development Team! Sea-Bird Scientific develops and manufactures high-accuracy instrumentation for the measurement of ocean parameters. Together we will drive innovation of new products and support the continued evolution of our established instrumentation. The core purpose of this role is to apply your electrical engineering knowledge, with some supervision or guidance, to the design, test, modeling and use of our products, subassemblies, complex systems, and platforms. The successful candidate will report directly to the Electrical Engineering Manager, based at the Bellevue, WA facility. Culture fit, shared values and a belief in our mission are as important to us as your technical ability. Salary will be commensurate with experience, within strictly define ranges.We need an engaged, talented Electrical Engineer to join our Product Development Team! Sea-Bird Scientific develops and manufactures high-accuracy instrumentation for the measurement of ocean parameters. Together we will drive innovation of new products and support the continued evolution of our established instrumentation. The core purpose of this role is to apply your electrical engineering knowledge, with some supervision or guidance, to the design, test, modeling and use of our products, subassemblies, complex systems, and platforms. The successful candidate will report directly to the Electrical Engineering Manager, based at the Bellevue, WA facility. Culture fit, shared values and a belief in our mission are as important to us as your technical ability. Salary will be commensurate with experience, within strictly define ranges. | 5/3/2023 |
| 4801 | Molecular Devices Westborough, MA Scientist I Bachelor’s Degree in biological science, chemical engineering, bioengineering, or relevant field. Master’s Degree preferred. Exp: 1+ years |
Pall has a range of single use bioreactors that is constantly being refined and updated to meet our customer needs. A position has become available for a Scientist I role in Pall’s Biotech R&D Bioprocessing team at the company’s New England Centre of Excellence in Westborough, MA. The team is responsible for process research support for new product developments within Pall. This individual will work closely with Pall colleagues, including R&D, product management, sales, and manufacturing to ensure Pall technologies continue to serve the evolving needs of our customers in the bioprocess industry. | 5/3/2023 |
| 4802 | Molecular Devices Marlborough, Boston, Cambridge, Shr, MA Bioprocess Engineer - Consumables Designer BS in Mechanical / biochemical / chemical engineering or a related engineering/life Science discipline. Exp: 1 year |
** This is a hybrid role with a 1 -4 days in the office a week** We are looking for a Bioprocess Engineer - Consumables Designer to work with our Enterprise Solutions Process and System Design (P&SD) team. Do you have a passion for Consumables Design? Then we would love to hear from you. | 5/3/2023 |
| 4803 | MP Biomedicals Solon, OH Production Chemist Bachelor of Science in Chemistry, Biochemistry, or Biology Exp: 0-3 years |
The production chemist will be trained on two different product lines. This position will rotate training through two manufacturing areas that include Immunology and Molecular Biology Liquids. Learn and be responsible for a wide variety of product formulation tasks. Follow and optimize production processes while following safety protocols. Produce quality research products in a timely fashion to meet customer demand. | 5/5/2023 |
| 4804 | DPT Laboratories Morgantown, WV Chemist I Bachelor's degree (or equivalent). Exp: 0-2 years |
Key responsibilities for this role include: Document laboratory activity in accordance with established procedures; including reagent preparation. Complete training as an Acquisition Controller on LC/MS systems. Demonstrate ability to understand and perform the major types of extraction methodologies employed within the lab Independently perform routine testing proficiently in accordance with all pertinent SOPs and lab practices Process and analyze data according to established procedures. Review data and associated documentation for compliance with Standard Operating Procedures. Operate analytical instrumentation including triple quadrupole HPLC-MS/MS systems and automated liquid handling workstations; including maintenance. | 5/5/2023 |
| 4805 | Nanostring Bothell, WA Manufacturing Research Associate I BS in Molecular Biology, Biochemistry, or related life science. Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. This position is Non-Exempt. | 5/5/2023 |
| 4806 | Nanostring Bothell, WA Manufacturing Research Associate I BS in Molecular Biology, Biochemistry, or related life science. Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. This position is Non-Exempt. | 5/5/2023 |
| 4807 | Nanosyn Santa Clara, CA Associate Research Scientist B.S. in Chemistry, Biochemistry or other relevant discipline. Exp: 0-2 years |
Develop new methods for the synthesis of organic molecules and prepare intermediates for the synthesis of these molecules. Apply modern techniques of organic synthesis including a variety of organic reactions at several scales, inert atmosphere techniques, thin-layer chromatography, NMR, LC-MS, HPLC, MS, flash chromatography, recrystallization, distillation, etc. | 5/5/2023 |
| 4808 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in Biology, Biochemistry or other relevant discipline. Exp: 0-2 years |
We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. The ideal candidate should have good organizational skills, possess good problem solving, communication and interpersonal skills and to adapt rapidly to new challenges. | 5/5/2023 |
| 4809 | NorthEast BioLab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: 1+ years |
Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices Follow appropriate safety and study requirements by reading, understanding, and following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) requirements, and Sponsor Study protocols Support business development and marketing activities, foster client relationships, and help onboard new sponsors | 5/5/2023 |
| 4810 | Nephron Pharmaceuticals West Columbia, SC FORMULATION TECHNICIAN I Associate or Bachelor’s Degree preferred Exp: 1+ years |
Position Summary: Dispense and formulate raw materials and operate compounding equipment used in the formulation of a final sterile pharmaceutical product Assist with additional work duties or responsibilities as evident or required | 5/5/2023 |
| 4811 | Nephron Pharmaceuticals West Columbia, SC Microbiology Quality Specialist Bachelor’s degree. Exp: 1 year |
Position Summary: Responsible for timely review of laboratory data, Standard Operating Procedures (SOPs), Equipment Validations, studies, and other documents related to the Microbiology department, as needed. Creates and executes project review plans; ensures timely completion of studies or assigned special projects to meet changing needs, requirements, and deadlines of the Microbiology department. Assists with additional work duties or responsibilities as evident or required. | 5/5/2023 |
| 4812 | Nexcelom Bioscience San Diego, CA Research Associate - Exploratory R&D B. S. or M.S. in Biology, Immunology or another related field. Exp: 1 year |
The Research Assistant will be involved in product development and optimization of cell culture process and new product development. In particular, he/she will be involved in determining the feasibility of new products and new cell culture processes for in-house and custom projects. This role will also be involved in troubleshooting issues associated with cell culture. This role requires mammalian cell culture experience. Knowledge of process development for antibody production, particularly hybridoma, on a small and large scale is a plus. He/she must have excellent organizational skills, attention to detail, and accuracy. Be able to maintain good documentation practices and generate reports. Must be proficient in computer software use (Excel, Word, and PowerPoint). Must be self-motivated and able to multi-task. Must be collaborative and have good communication skills. | 5/5/2023 |
| 4813 | Nexcelom Bioscience Pennington Reserve at Upper Provide, PA Research Specialist BS in Biology, Biochemistry or Chemistry. Exp: 1+ years |
We are looking for a highly motivated candidate to provide critical lab research support at a customer site in Upper Providence, PA. The Research Technician provides support to scientists by managing routine in-laboratory tasks according to Scope of Work (SOW) and specifications agreed on between R&D and PerkinElmer. The Research Technician could cover all or some of the following, and work in either GxP or non-GxP laboratory environments. The Research Technicians SOW will depend on demonstrated skills and experience. A successful candidate should have great attention to detail, outstanding organizational skills, and the ability to communicate effectively and be able to work independently. | 5/5/2023 |
| 4814 | Nexcelom Bioscience San Diego, CA Research Associate I - Diagnostics Bachelor’s degree in a Life Sciences-related field Exp: 1 years |
***Research Associate I and Research Associate II candidates will be considered** BioLegend is seeking a highly motivated Product Development Research Associate to join our Diagnostic Product Development Team. This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report. | 5/5/2023 |
| 4815 | Nexcelom Bioscience San Diego, CA Research Associate - Antibody Development Bachelor of Science with a discipline in cell biology, immunology, and biochemistry preferred. Exp: 1-2 yrs |
This person would be responsible for developing phosphosite specific monoclonal antibodies in BioLegend derived from immunized animals by performing antigen preparation, host immunization, bleed analysis, and cell lysate preparation. Techniques involved in this job include antigen formulation, animal immunization and tissue harvesting, cell culture and antibody analysis using ELISA and Western blot techniques. | 5/5/2023 |
| 4816 | Nexcelom Bioscience San Diego, CA Research Associate II- Cell Analysis Bachelor’s Degree in life sciences. Exp: 1+ years |
At BioLegend we develop novel, cutting edge products and offer custom services to help with scientific innovation and discovery. We are currently looking for a talented, detail oriented person to join our growing Product Development team. The potential candidate will assist with development of new products for cell analysis such as antibodies, multi-color panels, and reagents for analysis of cell metabolism and cell imaging. The successful candidate must be a self-motivated, team player, able to communicate effectively with a multi-disciplinary team and must possess excellent organization skills. | 5/5/2023 |
| 4817 | Nexcelom Bioscience San Diego, CA Research Associate - Exploratory R&D B. S. or M.S. in Biology, Immunology or another related field. Exp: 1 year |
The Research Assistant will be involved in product development and optimization of cell culture process and new product development. In particular, he/she will be involved in determining the feasibility of new products and new cell culture processes for in-house and custom projects. This role will also be involved in troubleshooting issues associated with cell culture. This role requires mammalian cell culture experience. Knowledge of process development for antibody production, particularly hybridoma, on a small and large scale is a plus. He/she must have excellent organizational skills, attention to detail, and accuracy. Be able to maintain good documentation practices and generate reports. Must be proficient in computer software use (Excel, Word, and PowerPoint). Must be self-motivated and able to multi-task. Must be collaborative and have good communication skills. | 5/5/2023 |
| 4818 | Novartis Cambridge, MA Research Scientist, Cell and Gene Therapy B.S in in Molecular/Cell Biology, Biochemistry or related field. Exp: 1+ years |
We are seeking a highly motivated scientist to join the Biotherapeutic Engineering and Gene Therapy (BEGT) group within NBC in Cambridge, Massachusetts. The BEGT group drives a diverse portfolio of modalities including therapeutic proteins, multi-specific antibodies, CAR-T, RNA therapeutics and AAV. Through innovative and rational protein design as well as cell and viral engineering, the BEGT group works collaboratively within NIBR to broaden the use of biologics into therapeutic applications where conventional antibodies have limitations. | 5/5/2023 |
| 4819 | Novartis San Diego, CA Research Scientist - In Vivo Pharmacology Bachelor's degree in biomedical research, neuroscience, animal behavior or animal sciences. Exp: 1+ years |
The Neuroscience Disease Area at Novartis is looking for a Research Scientist to perform tissue-based analysis in support of discovery and validation of disease relevant targets and pathways at the San Diego campus primarily focusing on gene therapies. | 5/5/2023 |
| 4820 | Novartis Cambridge, MA Research Scientist, Discovery & Translational Pharmacology BS or MS (or equivalent) in Life Sciences Exp: 1-2 years |
Your responsibilities include, but are not limited to: * Perform animal handling, dosing techniques & tissue collection * Implement ex-vivo bio-analysis on generated samples * Work independently to design, execute and analyze in vivo studies in line with project needs and timelines * Support the development of new in vivo models for chronic kidney diseases and systemic fibrosis * Work in a highly team-orientated and matrix environment * Clearly present results and data to teams within Disease Area X and across NIBR * Work in compliance with the Novartis Code of Conduct and in accordance with Novartis guidelines on health and safety and data recording | 5/5/2023 |
| 4821 | Novartis Cambridge, MA Research Scientist, Biochemistry - CVM MS degree in biochemistry, molecular or cell biology, biophysics, biomedical engineering or a related field; BS degree. Exp: MS: 0 years; BS: 1 year |
We are seeking a highly motivated in vitro Research Scientist to join our Biochemistry team. Here you will advance our understanding of disease biology and the discovery of new drugs, by contributing to target validation, assay development and drug screening efforts throughout the disease area and in collaboration with the larger research organization. | 5/5/2023 |
| 4822 | Novartis Emeryville, CA Research Scientist I, NITD Pharmacology Bachelor’s degree (B.A./B.S.) in biomedical or life sciences field preferred. Exp: 0-2 years |
The NITD Pharmacology group provides high quality in vivo research work and support to enable drug discovery research and development. We are looking for a Research Scientist I to coordinate and run in vivo research studies and projects to support the diverse and exciting project portfolio at NITD. The candidate should be action-oriented, skilled in experimental animal work, and possess a strong scientific background in order to plan, design, coordinate and perform in vivo experiments with high technical and ethical standards. The role will require an ability to work independently as well as in close collaboration with other research scientists. | 5/5/2023 |
| 4823 | Novo Nordisk Fremont, CA Engineer - R&D - CELL THERAPY Bachelor preferred. Degree within biomedical engineering, bioengineering, chemical engineering, or life sciences related area preferred. Exp: 0-1+ years’ |
The Cell Therapy R&D Engineer will help develop advanced cell therapeutics by driving product development activities for medical device and biologic/device combination products. The role is responsible for identifying, investigating, and assessing interactions between components of Novo Nordisk’s cellular products including cells, formulations, and medical devices. The Cell Therapy R&D Engineer works closely with product development teams to evaluate device robustness, assists with specifications and product development, and performs testing. This individual will be the subject matter expert for multiple cell and device evaluation equipment systems chosen by Novo Nordisk for product development. | 5/5/2023 |
| 4824 | Novo Nordisk West Lebanon, NH Cell Therapy Associate Master’s in Cell Biology, Molecular Biology or a closely related field. Exp: one (1) year |
This position has the responsibility of working with senior level Scientists and manufacturing associates to execute process development, scale-up, tech transfers, and validation studies in support of manufacturing or analytics. Additionally, the role will necessitate experimental troubleshooting, GMP documentation and laboratory investigations. The position will require understanding the underlying science of the process and manufacturing equipment, or assay methods and instruments. This position is located in West Lebanon, New Hampshire and will require onsite work. It is a full time (40 hours per week) position and the standard schedule is Monday-Friday 8am to 5pm. | 5/5/2023 |
| 4825 | Novo Nordisk West Lebanon, NH Quality Control Microbiologist Bachelors in a scientific discipline. Exp: 1 year |
This position has primary responsibility to support QC operations in the microbiology or analytical area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This position carries out routine QC testing and may support sampling, investigations, validations, projects and other related support activities for the manufacturing facility and process. This individual works with supervision on routine tasks and detailed instruction on new tasks. This position is located in West Lebanon, New Hampshire and will require onsite work. It is a full time (40 hours per week) position and the standard schedule is Tuesday-Saturday 8am to 5pm. | 5/5/2023 |
| 4826 | Novo Nordisk West Lebanon, NH Manufacturing Science and Analytical Technology Associate I Bachelor’s degree or equivalent in Biochemistry, Chemistry, Engineering or a closely related field. Exp: one year |
This position has the responsibility of working with senior level Scientists to execute laboratory scale process development or validation studies in support of process or assay development, or process troubleshooting or scale-up. The scientific knowledge in this position will range from familiarity with details of manufacturing process, process chemistries, development studies and relevant assay methods and instruments. This position will be one of the interfaces between MSAT and Manufacturing or Quality. | 5/5/2023 |
| 4827 | Novo Nordisk Clayton, NC Manufacturing Engineer BS in Engineering/related field. Exp: 0-2+ years |
Learning the core processes & methods to improve system & equipment reliability to meet all customer, business & regulatory requirements through the following activities: People Focus, Process Focus, Equipment Focus & Standards “Gatekeeper”. | 5/5/2023 |
| 4828 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 5/5/2023 |
| 4829 | Ocean Ridge Biosciences Concord, OH Lab Technician/Associate Scientist - Genetic Toxicology Bachelor’s degree in biology, microbiology, chemistry or other related field. Exp: 1+ years |
This position will provide technical support for performing standard genetic toxicology assays to include, but not limited to cell-based assays, bacterial reverse mutation assay, rodent (rat and mice) bone marrow and blood based micronucleus assay, as well as other in vitro-related activities. | 5/5/2023 |
| 4830 | Ocean Ridge Biosciences Concord, OH General Lab Technician Required qualifications are a B.S. in a chemistry or related field. Exp: 1+ years |
The ideal candidate will perform general lab functions in support of preclinical drug development/ agrochemical studies in a GLP environment. | 5/5/2023 |
| 4831 | Ocean Ridge Biosciences Exton, PA Lab Technician, BGC Bachelor’s degree in molecular biology, Biology, Biochemistry, Chemical Engineering, Mechanical Engineering, or equivalent. Exp: 1-5 years |
We are looking for a qualified Lab Technician to join our team. The role will perform and support laboratory procedures and controls within Biologics, Gene, and Cell Therapy (BGC) Department to maintain efficiency and compliance for the laboratory. The ideal candidate needs to have an entrepreneurial spirit that enables her/him to wear multiple hats as we scale-up the laboratory business. The candidate will have experience in working in a laboratory environment, preferably within biologics/or GCT lab. The candidate will be well-trained to maintain safety conditions in the lab and expected to be passionate in working in a matrix organization environment. The goal is to optimize lab compliance and maintaining the smooth running of the lab. | 5/5/2023 |
| 4832 | Ocean Ridge Biosciences Concord, OH Entry Level Lab Chemist Required qualifications are a B.S. in a chemistry or related field. Exp: 1+ years |
This position is for an entry level lab chemist. The ideal candidate will help support studies of preclinical drug development in a GLP environment. | 5/5/2023 |
| 4833 | Ocean Ridge Biosciences Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields. Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 5/5/2023 |
| 4834 | Ocean Ridge Biosciences Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree. Exp: 0-3 years |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 5/5/2023 |
| 4835 | Ology Bioservices Alachua, FL Specialist II, Biomanufacturing (Relocation) B.S. (Science or Engineering) Exp: one year |
Responsibilities and Authority: This position will perform production related activities in the cGMP Manufacturing Core according to established procedures at the Manufacturing Facilities in Alachua (Florida). Perform upstream related activities including cell culture at small and large scale, cell transfection, media and buffer preparation, and bioreactor and fermenter-based production. Perform downstream related activities including chromatography purification, centrifugation and ultracentrifugation, ultrafiltration/diafiltration, and viral clearance. Draft Standard Operation Procedures, Change Controls, and Deviations. Properly disinfect and stage materials into production rooms before the production campaigns. Perform with ordering equipment, installation, qualification, and routine maintenance. Draft and review Production batch records and review executed records. | 5/5/2023 |
| 4836 | Pacific Edge Hummelstown, PA Laboratory Technician Bachelor's degree in medical technology, chemical, physical, or biological sciences. Exp: 1 year |
Pacific Edge Diagnostics USA, an innovative cancer detection testing company is a talented Clinical Laboratory Technician to join this rapidly growing company. The Clinical Laboratory Technician's primary responsibility will be to perform molecular clinical testing (from specimen receipt through reporting patient results), as well as general lab maintenance. | 5/5/2023 |
| 4837 | Pacira Biosciences San Diego, CA Microbiologist 1 BS degree in Microbiology or other life science. Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products. | 5/5/2023 |
| 4838 | Key Tech Baltimore, MD Electrical Engineer (Full-Time & Intern Positions) BS or MS Electrical Engineering degree from leading university/college Exp: Up to five years |
We’re actively hiring for full-time engineers as well as spring, summer and fall interns (electrical, computer, and mechanical) with competitive well paid salaries and benefits. Our interns work on real engineering challenges from day one. Everyone who starts at Key Tech jumps right into interesting, creative high tech work. With a blend of challenging work, smart coworkers, and the best company culture, Key Tech is the right company for you. | 4/24/2023 |
| 4839 | Khloris Biosciences Mountain View, CA Cell Therapy Manufacturing Technician B.S. degree in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience. Exp: 0-5 years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated cell therapy manufacturing technician to join our team. The selected candidate will work closely with lead manufacturing technicians, scientists, participate in project and team meeting, and work in a multidisciplinary environment. The duties of this position will involve supporting a multidisciplinary manufacturing team in developing Khloris cell therapy platforms. The ideal candidate will have hands-on expertise and comprehensive understanding of cell therapy manufacturing processes. | 4/24/2023 |
| 4840 | Lantheus Medical Imaging Billerica, MA Research Scientist I MS in Chemistry, Pharmaceutics, Engineering or equivalent. Exp: 1-2 years |
Radiochemist/Chemist to conduct radiolabeling studies to support R&D portfolio of new and existing products. Requirements include technical expertise in optimization and troubleshooting of synthesis processes, interaction with and transfer of radiolabeling methodology to contract manufacturing sites, and competency in use of HPLC, UV, radio-detection, LCMS and iTLC methodology. Handling of positron and gamma radionuclides for small scale radiolabeling experiments and analytical analysis of both research and commercial products is required. Communication with contract research organizations required for external studies using R&D test compounds. Data interpretation, issue resolution as needed and final report writing is also required. | 4/24/2023 |
| 4841 | Locus Biosciences Research Triangle Park, NC Preclinical Research Technican BS in biology, chemistry, microbiology, microbial genetics, synthetic biology, genetic engineering or similar fields. Exp: 1-5 years |
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Research Technician within the Preclinical Animal Models team. This position is well-suited for highly motivated technicians that have a desire to push product development forward into critical preclinical in vitro and in vivo testing across a variety of therapeutic indications. This individual will work directly with scientists in the R&D Department to develop and execute in vivo animal models and analyze tissue samples using various molecular and biochemical assays. The ideal candidate will be well organized and have a scientific background as well as experience with microbiology techniques and in running animal models. Candidates must have the ability to manage multiple concurrent projects, but be flexible, adjusting plans as the data dictates. The individual must be able to communicate effectively and be able to work across interdisciplinary teams. | 4/25/2023 |
| 4842 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Synthesis -Swing Shift (49908) Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Synthesis will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Synthesis department. Swing Shift T-F 10a.m. 4/10 hour shifts | 4/26/2023 |
| 4843 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Pilot Synthesis - Day Shift (4... Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Synthesis will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Synthesis department. Day Shift M-F 7-3:30p.m. 8 hour shifts | 4/26/2023 |
| 4844 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Purification- Day Shift (49910) Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Purification will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Purification department. Day Shift - 7a.m. to 5:30p.m. Tuesday through Friday 4/10's | 4/26/2023 |
| 4845 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Purification- Swing Shift (49911) Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Purification will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Purification department. Swing Shift Tuesday - Friday 10a.m. to 8:30p.m. 4/10's | 4/26/2023 |
| 4846 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Liquid Handling- Day Shift (49... Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Liquid Handling will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Liquid Handling department. Day Shift M-F 8 hour shifts | 4/26/2023 |
| 4847 | Lucigen Petaluma, CA MSAT Chemist (49589) Bachelors in Science required / Masters in Science preferred in Chemistry, Chemical Engineering or related discipline. Exp: 1 year |
We are looking for a highly motivated chemist, biochemist and/or chemical engineer to join in our newly commissioned state-of-art therapeutic oligonucleotide GMP manufacturing facility in Petaluma, CA. This individual will work in a Process Development lab to support therapeutic oligonucleotide manufacturing process development, transfer, and trouble-shooting production issues. | 4/26/2023 |
| 4848 | Lung Biotechnology Silver Spring, MD Associate I, API Production/Synthetic Chemistry Bachelor’s Degree in Arts/Sciences (BA/BS) in physical or biological sciences. Exp: 1+ years |
Responsible for the production of active pharmaceutical ingredients (API) for three of United Therapeutics' commercial drugs, and other drugs that are in the development phase. This role will perform the production in a kilo lab setting using specific procedures and batch records following US and International guidelines for good manufacturing practices (cGMP) to ensure high-quality production. | 4/26/2023 |
| 4849 | Lykan Bioscience Hopkinton, MA QC Analyst, Microbiology Certificate in Biotechnology or Bachelor's degree in scientific discipline preferred. Exp: 0-7+ years' |
The Quality Control Analyst will be responsible for collection of environmental and raw material samples, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. | 4/27/2023 |
| 4850 | Lykan Bioscience Hopkinton, MA Cell Processing Associate Bachelor's degree in biology or related scientific discipline. Exp: 0-2 years |
Reporting to the Manufacturing Supervisor, this position's core responsibilities are focused on manufacturing processes related to cell therapies. Activities include aseptic sampling of product in a Biosafety Cabinet (BSC) in an ISO V environment, operation of incubators in an ISO VII environment, as well operating automated, single-use systems for the targeting, expansion and harvesting of cells. The Cell Processing Associate will also collaborate as needed with peers within Manufacturing Sciences and Technology (MST), Quality and Facilities. | 4/27/2023 |
| 4851 | Lyophilization Services of New England Bedford, NH QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study. Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 4/27/2023 |
| 4852 | Marker Therapeutics Houston, TX Cell Therapy Manufacturing Technician BS, MS in Biology or a related science. Exp: 1-5+ years |
Marker Therapeutics is seeking a cell therapy technician for its manufacturing group to support its ongoing efforts to develop immunotherapies for the benefit of patients with cancer. This position will work under the guidance of the Senior Director of CMC and perform assigned responsibilities to support the company’s product manufacturing process and process improvement initiatives. Depending on previous experience and qualifications, this individual will be expected to either lead or support the manufacturing process and process characterization of scale-up/scale-down cell manufacturing processes, including optimizing process parameters, cell concentrations and therapeutic product fill and finish technologies to advance our therapeutic programs. The successful candidate must be a team player with strong expertise in GMP manufacturing and must have the ability to communicate and collaborate within an interdisciplinary environment. | 4/27/2023 |
| 4853 | MatTek Ashland, MA Production Associate I Bachelor’s degree in Biology or equivalent Exp: no previous |
Description: Participates in duties associated with manufacturing of MatTek tissue models according to SOPs where applicable. May also perform duties assigned under Laboratory Assistant as needed. Reporting structure: Works under the direction of more senior Associates and the Laboratory Supervisor/Manager. Reports directly to the Laboratory Supervisor/Manager or Scientist/Senior Scientist. | 4/27/2023 |
| 4854 | Maverick Therapeutics Boston, MA Cell Processing Technician/Specialist Bachelor's degree in biotechnology, biology, engineering or related pharmaceutical science. Exp: 0+ years |
As a Cell Processing Technician/Specialist, working on the Cell Therapy Manufacturing team, you will be empowered to support the manufacturing of Takeda's Cell Therapy products and work with peers to support clean room activities. The main focus of your role will be cGMP cell therapy manufacturing at Takeda's new cell processing facility in Cambridge, Massachusetts. You will directly contribute to the delivery of novel cell products to support human clinical trials. This is an On-Site role.\ | 4/27/2023 |
| 4855 | Maverick Therapeutics San Diego, CA Research Associate II, Global Biologics MS in Molecular Biology, Biochemistry, or related life science. Exp: 0+ years |
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible to bring life-changing therapies to patients worldwide. Join Takeda as a Research Associate II where you will perform research assignments and be responsible for high-throughput antibody production. You will also work on the discovery and engineering of therapeutic biologics including antibodies, antibody fragments, and fusion proteins. As part of the Biotherapeutic Engineering team, you will report to Scientist II, Biotherapeutic Engineering, where you will interpret and communicate results within the team and with cross-functional project team members. | 4/27/2023 |
| 4856 | Maverick Therapeutics Boston, MA Research Associate II Invitro/Exvivo VD1 Biology MS in a scientific discipline. Exp: 1-2 yrs+ |
The Cell Engager Team of the Oncology Drug Discovery Unit is looking for an enthusiastic lab-based research associate to support the characterisation of antibodies and immune engagers within the Cell Engager portfolio to deliver work packages related to various projects. The work will include the development and running of biological assays to characterise the antibodies, and other biologic entities, the preparation and maintenance of primary and cell line cultures and contribution to the smooth running of the laboratory. The role is laboratory-based within a dynamic cross-functional R&D team. The selected candidate will be expected to conduct routine lab assignmens and protocols; contributes to design of and implementation of improvements for routine procedures | 4/27/2023 |
| 4857 | Merieux NutriSciences Minnetonka, MN Laboratory Technician Bachelor's degree required. Exp: 0+ years |
The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. | 4/27/2023 |
| 4858 | Merieux NutriSciences Crete, IL Chemist 1 Bachelors preferred. Exp: One - two years |
Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. Wash glassware as needed and prepare samples as needed. Prepare standards or reagents that are needed for the analysis procedure. Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. Initiate and investigate customer complaint and non conformances Determine root cause and corrective action | 4/28/2023 |
| 4859 | Merieux NutriSciences Salt Lake City, UT Chemist 1 Bachelors preferred. Exp: One - two years |
Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. Wash glassware as needed and prepare samples as needed. Prepare standards or reagents that are needed for the analysis procedure. Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. Initiate and investigate customer complaint and non conformances Determine root cause and corrective action | 4/28/2023 |
| 4860 | Merieux NutriSciences Crete, IL Chemist III Masters degree. Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food, pharmaceutical, and other sample. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the sample to obtain the required results. The incumbent observes daily activities of departmental personnel ranging from receiving to reporting of results and ensures that analysis is performed correctly. The incumbent is responsible for performing chemical analysis on food, pharmaceutical, and other sample. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the sample to obtain the required results. The incumbent observes daily activities of departmental personnel ranging from receiving to reporting of results and ensures that analysis is performed correctly. | 4/28/2023 |
| 4861 | Mesa Biotech Florence, SC Analytical R&D Scientist I Bachelor’s degree in chemistry or related field required. Exp: 1-2 years |
The Scientist I conducts laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Utilizes judgment in making adaptation and modifications on all assignments. Provides routine analyses in an analytical chemistry laboratory following standard practices. Performs analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results | 4/28/2023 |
| 4862 | Mesa Biotech San Francisco, CA Cell Therapy Specialist Bachelor’s or Associates degree in a technical field desired. Exp: 1+ years |
Thermo Fisher Scientific is making a significant investment in the dynamic and rapidly growing Cell Therapy space. Our Cell Therapy organization within the Pharma Services Group, is one of the fastest growing areas of Thermo Fisher Scientific. We focus on providing development and clinical scale services for gene and non-gene modified cell processing for a variety of unmet medical needs. | 4/28/2023 |
| 4863 | Mesa Biotech Middleton, WI Associate Chemist - 2nd Shift Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
2nd shift position (2-10pm) Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 4/28/2023 |
| 4864 | Mesa Biotech Middleton, WI Associate Scientist - Bioanalytical Lab Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 4/28/2023 |
| 4865 | Mesa Biotech Boston, MA Associate Scientist / Scientist – HPLC , CE Bachelor's degree in Biology, Analytical Chemistry, Biochemistry, Cell & Molecular Biology, Chemical Engineering, or equivalent and relevant formal ac Exp: Associate Scientist: 0-2+ years |
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. | 4/28/2023 |
| 4866 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus.Bachelor’s degree in life sciences, or related area is require Exp: 1+ years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. · Executes experiments and implements plans under close guidance utilizing established protocols. · Assists in data analysis and the preparation of experimental reports and/or presentations. · Participates in general lab maintenance initiatives including but not limited to maintaining laboratory supplies and equipment, maintaining electronic inventory list database, physical inventory, processing/aliquotting/vialing/labeling materials, and preparing and maintaining reagent inventories. | 4/28/2023 |
| 4867 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus.Bachelor’s degree in life sciences, or related area is require Exp: 1+ years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. · Executes experiments and implements plans under close guidance utilizing established protocols. · Assists in data analysis and the preparation of experimental reports and/or presentations. · Participates in general lab maintenance initiatives including but not limited to maintaining laboratory supplies and equipment, maintaining electronic inventory list database, physical inventory, processing/aliquotting/vialing/labeling materials, and preparing and maintaining reagent inventories. | 4/28/2023 |
| 4868 | Meso Scale Discovery Rockville, MD Engineer I, Process Bachelor’s degree in chemical/biochemical engineering or related field. Exp: one year |
Responsible for developing, characterizing and validating manufacturing processes to produce biochemical assay plates and related consumables. | 4/28/2023 |
| 4869 | Meso Scale Discovery Gaithersburg, MD Cell Culture Specialist I Bachelor's degree in Biology, Chemistry, Biotechnology, Engineering or a related field. Exp: six months |
This position is responsible for the production of cell-based products including but not limited to hybridoma antibodies and recombinant antibodies. | 4/28/2023 |
| 4870 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1+ years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. · | 4/28/2023 |
| 4871 | Metabolon Morrisville, NC Medical Lab Scientist 1 BS degree in a life science. Exp: 0-2 years |
Due to our rapidly growing services business, Metabolon is seeking a Medical Laboratory Scientist to work within the Platform Analysis group as an integral member of our Global Metabolomics Services team. The team member in this position will be responsible for all aspects of routine laboratory testing using our liquid chromatography–mass spectrometry (LC-MS) based instrumentation. The ideal candidate will have experience in LC-MS and will be expected to contribute to continuous improvement initiatives as required. In addition, the candidate will have a successful laboratory performance track record contributing as a team player in high throughput clinical laboratory testing environment. | 4/28/2023 |
| 4872 | Microbiologics Saint Cloud, MN Production Innovation Lab Technician, Saint Cloud Four (4) year degree in relevant field (e.g., biology, microbiology, virology, cell biology, molecular biology, food science). Exp: 1-year |
We are currently looking to add a Production Innovation Lab Technician to our team in St. Cloud, MN. In this role you will Assist with supervised experiments using microbiology techniques as well as other applicable methodologies leading to new products or process improvements. Generally required to apply education and work experience to conduct focused research thoughtfully, collaboratively, and efficiently with high integrity. | 4/28/2023 |
| 4873 | Microbiologics Saint Cloud, MN Quality Control Lab Technician, Saint Cloud Four-year microbiology or related degree required. Exp: 1+ years |
We are currently looking to add a Quality Control Lab Technician to our St. Cloud, MN team. In this role, you will perform Quality Control Testing, Shelf-Life Testing, and Packaging Event Evaluations on Microbiologics products in accordance with the appropriate Company Device Master Record (DMR), policies and procedures with the objective to release only production products that meet all of Microbiologics acceptance criteria. | 4/28/2023 |
| 4874 | Mirus Bio Madison, WI Laboratory Technician - Temporary College courses related to Biology and Chemistry preferred. Exp: 1+ years’ |
We are seeking a full time Laboratory Technician with an interest in biotechnology to perform general laboratory support duties, equipment maintenance, dispensing reagents, and labeling vials/bottles. This position will report to the Production Supervisor, and work closely with Quality, Shipping and R&D departments. | 4/28/2023 |
| 4875 | Moderna Therapeutics Norwood, MA Engineer I, Process Development BS or MS in chemical engineering, biological engineering, chemistry, biochemistry, or closely related field. Exp: 0-2 years |
This role will support the development of manufacturing processes for Moderna’s mRNA-based medicines to enable clinical and commercial supply, with a focus on process understanding and process control strategy definition, and the optimization, transfer, and characterization of manufacturing processes. The role will additionally interface with and support cross-functional teams across CMC, Research and Development, Pre-clinical and Clinical Manufacturing, Quality, and Analytical Development. Applicants must have demonstrated experience in designing, executing, and analyzing scientific experiments. Relevant academic and/or industrial experience in drug substance or drug formulation/delivery development is ideal. Previous experience with chromatography, nanoparticle formulations, filtration technologies, mixing technologies, and/or statistical design of experiments is preferred. | 4/28/2023 |
| 4876 | Moderna Therapeutics Norwood, MA Manufacturing Associate I Requires BA/BS in a relevant science or engineering discipline. Exp: 1+ years |
Moderna is seeking a highly driven individual for a Manufacturing Associate I position within High Throughput Operations (HTOps), at the Moderna manufacturing site in Norwood, MA. The HTOps team is responsible for high throughput production of mRNA and LNP in support of Moderna’s research portfolio. This position is Monday-Friday 7am-3pm shift. The individual hired into this role will independently execute DNA, RNA, and/or LNP unit operations following standard operating procedures. This individual is expected to be detail oriented and adhere to good laboratory practices, with a goal of manufacturing high quality DNA, RNA and LNP. In addition to daily production, the Manufacturing Associate I will be responsible for escalating issues experienced while processing. They are expected to take the initiative to learn the science behind the process that is being run, to fundamentally understand the process steps. The Manufacturing Associate I is expected to have a team mentality and respects the common work areas. They help to maintain the cleanliness, and 5S initiatives put into place in the lab in common areas as well as unit assigned areas. Commitment and active participation in the safety culture is required. In addition to a focus on manufacturing and maintaining the lab, it is strongly desired that the individual actively participates in the department’s continuous improvement and optimization initiatives. The successful candidate must demonstrate the ability to quickly master new processes and have the drive to be part of a dynamic, fast paced, and highly engaged and motivated team. | 4/28/2023 |
| 4877 | Moderna Therapeutics Norwood, MA Research Associate, Nucleic Acid, Process Development BS or MS in Chemical or Biochemical Engineering, Biology, Biochemistry, or closely related field. Exp: up to 3 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. DNA Process Development, a team residing in Moderna’s Technical Development organization, has been tasked with development and implementation of processes to produce DNA and enzymes utilized in the production of RNA. Our efforts in this area are growing, and Moderna is seeking a new team member to join the DNA Process Development team for a position based at the Norwood, MA site. In this role, you will have the opportunity to help develop new processes to facilitate rapid DNA and mRNA production at Moderna, with a focus on applying state of the art molecular biology and automation technologies. The incumbent will collaborate closely with the nucleic acid process development and process automation teams to develop new technologies for application in plasmid DNA manufacturing. Our goal is to enable clinical studies and to support commercial manufacturing, so you will work closely with multiple functions spanning development, technical operations and manufacturing. | 4/28/2023 |
| 4878 | Fresenius Kabi Melrose Park, IL Scientist I Bachelor of Science in Chemistry, Biology or related physical science. Exp: 1+ years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 4/18/2023 |
| 4879 | Fresenius Kabi Melrose Park, IL Scientist I Bachelor of Science in Chemistry, Biology or related physical science. Exp: 1+ years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 4/18/2023 |
| 4880 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 2nd Shift Chemistry Possess a B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 4/18/2023 |
| 4881 | Fresenius Kabi Melrose Park, IL Manufacturing Engineer Bachelor’s degree in Engineering (Electrical, Chemical, Controls, Computer, Mechanical, etc.). Exp: 1-3 years |
Responsibilities include using technical expertise in support of daily operations in aseptic filling or formulation by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity. Apply accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyze situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 4/18/2023 |
| 4882 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift Chemistry Possess a B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 4/18/2023 |
| 4883 | Fresenius Kabi Wilson, NC MQA SPECIALIST II (NIGHTS) Bachelor of Science degree Exp: 1-3 years |
Performs routine audits of manufacturing areas to ensure product quality and SOP/GMP compliance at the Wilson Manufacturing Facility. Assists in troubleshooting manufacturing problems and inspection defects. Provides plant support for collection of data where needed, while assembling required metrics for review by facility management. Updates controlled documents, including SOPs, policies and batch records to maintain compliance in the production areas. | 4/18/2023 |
| 4884 | Galatea Surgical Research Triangle Park, NC Senior Scientist (Onsite - Durham, NC Research Triangle Park) Graduate degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Materials Science & Engineering, Polymer Science, Textiles or related fie Exp: 0-5 years |
The incumbent will carry out experimental studies relating to drug/device combination technology within the Interventional Innovation R&D team at BD Technologies and Innovation (BDTI) with an initial focus on BD’s Interventional business segment. Specifically, the candidate will guide in drug formulation and delivery technologies, soft materials characterization, and drug-biomaterials-tissue interactions. They will work with project team members to plan and implement technical assessments of coatings for medical devices and drug delivery technologies/products. Additional areas for technical assessment may be included as well, for example, biocompatible implants and materials for use in surgical procedures. They will be responsible for the execution of technical work and communication of results to various collaborators. Additional responsibilities include investigating and resolving technical problems and managing different workstreams to meet program objectives and timelines. The candidate will author/review SOPs, test/project reports, and other documents as required to implement studies in the laboratory. The incumbent is expected to work closely with other R&D project team members and support functions within BDTI and BD business units, contribute intellectual property, create experimental designs/test methods, and analyze experimental data. They will work with project team leadership to help ensure a smooth transition of projects from the Innovation phase to product development. | 4/18/2023 |
| 4885 | DVC LLC Atlanta, GA Scientist - Laboratory and Specimen Management MS in Microbiology or Biology Exp: 0-2 years |
GDIT is currently seeking a Scientist with microbiology background supporting research, diagnostics, and surveillance activities for a team focused on influenza pandemic preparedness for the CDC in Atlanta GA.This role may be required to perform preparation, culture, and characterization of viral or bacterial strains or mammalian cell lines using a wide range of techniques and approaches. You will assist in maintenance of laboratory supplies and reagents including ordering, receiving, stock preparation and validation of reagents, solutions, and standards prior to use. The desired candidate will be able to work well with a diverse workforce within the Immunology and Pathogenesis Branch (IPB) as well as other branches in Influenza Division.This position is located on the Roybal Campus in Atlanta, Georgia. | 4/18/2023 |
| 4886 | GenScript Pisctaway, NJ Research Scientist – Automated Process Development MS in Biology/ Biochemistry/ Molecular Biology/ Biomedical Instrumentation/ Bioengineering Discipline or related subjects. Exp: 1 year |
We are looking for a Research Scientist – Automated Process Development to support the key high throughput molecular biology reagent production needs in the US Molecular Biology/ Reagent services business unit. | 4/18/2023 |
| 4887 | Glaukos San Clemente, CA MANUFACTURING TECHNICIAN II - PHARMA OPERATIONS bachelor’s degree in science or engineering Exp: 0 – 2 years’ |
The Manufacturing Technician II, based in San Clemente, CA, will perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality system regulation (QSR) medical device good manufacturing practices (GMP) requirements. | 4/18/2023 |
| 4888 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Microbiology Technician (2nd or 3rd shift) Bachelor’s degree in microbiology or a related field Exp: 0-2 years’ |
The Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. | 4/19/2023 |
| 4889 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Chemist - 3rd Shift Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology). Exp: 1 years |
The QC Chemist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 4/19/2023 |
| 4890 | Greenlight Biosciences Lexington, MA Biomanufacturing Associate BS/BA in Biotechnology, Microbiology, Cell Biology, Chemical Engineering, Biochemistry or equivalent Exp: 0+ years |
We are seeking a Biomanufacturing Associate for a manufacturing role to start-up and run day to day operation of GreenLight’s cGMP manufacturing operations in Lexington, MA. This individual will initially assist in the installation and qualification of biomanufacturing equipment leading into the production GMP materials in support of GreenLight’s portfolio. They will be tasked with being part of a dynamic manufacturing team scaling up and producing RNA material under GMP conditions in support of Clinical operation. The position offers growth potential for a very experienced manufacturing associate or someone just starting off their Biotech career with a growing biomanufacturing team within a growing company. | 4/19/2023 |
| 4891 | GRO Biosciences Cambridge, MA RA/Senior RA, Application Sciences MS degree or BS/BA degree in biology, microbiology, biochemistry, biotechnology, synthetic biology, systems biology, biological engineering, or relate Exp: BS: 1 year |
GRO Biosciences (GRObio) is hiring a Research Associate (RA) or Senior RA to develop novel protein therapies produced from the company’s recoded organism platform. Recoded organisms bear an expanded genetic code and enable GRObio to generate revolutionary products of unprecedented structural and chemical diversity. With the tools at GRObio, you’ll be able to propose, develop, and implement completely differentiated solutions to longstanding, critical problems. GRObio is seeking a motivated team-player and problem-solver to contribute to preclinical product development within Application Sciences. Ideal candidates thrive in new areas, can “wear many hats”, and will enjoy an outsized impact on the growth of an early-stage company. Regular activities will include planning and carrying out experiments throughout our pipeline, including strain development, biomass generation, protein purification, protein characterization, and bioassays. This position will interface heavily with team members from other groups, including collaborations with automated R&D divisions to realize rich datasets. There is substantial growth opportunity within the company for the capable candidate. | 4/20/2023 |
| 4892 | HelixBind Boxborough, MA Formulation Technologist Certificate, Associate’s or Bachelor’s degree in a science or engineering discipline. Exp: 0-5 years’ |
We are seeking a talented and motivated individual to join our R&D Team as a Formulation Technologist. This is a great time to join our team. The position offers the exciting opportunity to grow along with the Company as we take our initial product through FDA clearance and market launch while, in parallel, build out our pipeline of impactful syndromic diagnostic assays. | 4/20/2023 |
| 4893 | Heska Des Moines, IA Technician I, II or III, Bacterins Bachelor’s Degree in a science or bio-technology field. Exp: Technician I: 1 year |
The Bacterins Technician I position will work under the close supervision of the Bacterins supervisor to foster the growth of bacterial cultures through fermentation and cell media preparation while maintaining a sterile environment. This position requires the ability to multi-task and follow standard operating procedures. Technican level will be based on revelant experience. | 4/21/2023 |
| 4894 | i2O Therapeutics Cambridge, MA Research Associate (in vivo) AA/AS/BA/BS in a science field Exp: 1 year |
i2o Therapeutics is a biotech startup developing a drug delivery platform to convert injectable therapies into oral modalities. This full-time, hourly position includes conducting and assisting with in vivo studies to support a variety of projects within a small, multi-functional team | 4/21/2023 |
| 4895 | Integrated DNA Technologies Coralville, IA Research Scientist II-Enzyme Development Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field). Exp: one or more years |
The Research Scientist II, under minimal direction, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with the development and characterization of new IDT protein products in the CRISPR, qPCR, and NGS domains. This position is responsible for planning and executing experiments, analyzing data, and reporting/presenting findings as well as supporting IDT customers. A background in bacterial genetics and/or protein engineering is highly preferred. This position is equivalent to a Research Assistant II position at an academic institution. | 4/21/2023 |
| 4896 | Integrated DNA Technologies Danvers, MA Research Associate BSc or BA in a Scientific discipline Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure. | 4/21/2023 |
| 4897 | Inova Diagnostics Orangeburg, NY BioReagent Technologist I BS in a Science field or related technical discipline Exp: up to two years |
Responsible for the isolation and purification of proteins from recombinant and natural sources. | 4/21/2023 |
| 4898 | Inova Diagnostics Orangeburg, NY BioReagent Technologist I BS in a Science field or related technical discipline Exp: up to two years |
Responsible for the isolation and purification of proteins from recombinant and natural sources. | 4/21/2023 |
| 4899 | Inova Diagnostics San Diego, CA Chemist IFA Slides - AID Bachelor's degree (B.A.) or (B.S.) in the biological, chemical or related sciences Exp: 0-1 years |
The IFA Slides department is looking for a candidate to be apart of a fast-paced, supportive manufacturing team to assist with preparation of autoimmune diagnostic Immunofluorescence Assays (IFA) cell culture slide products. Opportunites for advancement and career growth while performing, mammalian cell culture, immunofluorescence cell suspension and slide preparation activities. | 4/21/2023 |
| 4900 | Inscripta Pleasanton, CA Research Assistant/Research Associate I, Synbio Bachelor’s degree in a scientific discipline or associate degree from a laboratory science or biotechnology program will be considered. Exp: 1+ year |
The Research Assistant/Research Associate I will primarily assist in lab management services such as media preparation, inventory, and shipping & receiving activities. They will report directly to the Laboratory Manager but will have opportunities to cross train and support other groups such as Screening, Analytic Chemistry, and Strain Banking. The successful candidate will be a team player who works within the group to meet department goals, objectives, and tasks to achieve desired results. They can respond to new requests with appropriate urgency and an organized approach and hold themselves accountable to fulfill assigned tasks and achieve results within assigned timelines. | 4/21/2023 |
| 4901 | Integral Molecular Philadelphia, PA Research Associate - (Job ID# 04182023) Bachelor’s degree in biology, bioengineering, or a related field Exp: 1–2 years |
Our close-knit, medium-sized company is composed of smart, curious, diverse scientists who take an active interest in the scientific and technical development of our team members. We seek a Research Associate I to join our dedicated group of scientists. A desirable candidate will have the skills to culture mammalian and/or bacterial cells, perform DNA mini-preps, and complete bacterial transformations and cell transfections. Familiarity with flow cytometry is an added bonus! | 4/21/2023 |
| 4902 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I, Lab Support [Contract to Hire] Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1 year |
Iovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. Iovance is seeking a Quality Control (QC) Laboratory Support Analyst I who will assist the Laboratory Manager with the day-to-day upkeep of the QC laboratories including but not limited to collecting data for trending, maintaining positive control inventories for various QC assays, and uploading assay records to the document management system. The ideal candidate will have experience working in a GMP-regulated laboratory with pipetting knowledge but is not required. The position will report to the Lab Support Manager, Quality Control. | 4/21/2023 |
| 4903 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst, Microbiology (Weekend shift) [Contract to Hire] Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: one (1) year |
The Quality Control Analyst will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques. This position will work a weekend shift (10 hr shifts Wed-Sat) to support manufacturing weekend activities. | 4/21/2023 |
| 4904 | iRhythm Technologies Cypress, CA Manufacturing Engineer II Bachelor’s Degree in Engineering or a related field required Exp: 1-3 years |
iRhythm Technologies has an opening for a full-time technical expert in manufacturing engineering. The Senior Manufacturing Engineer will provide manufacturing support for existing products and processes as well as new products, product changes, line extensions and enhancements including all associated equipment validation. In this dynamic environment you will have the opportunity to develop your technical skills and leadership competencies in the MedTech and wearable device industry while advancing your career. Our work environment is fast paced, with a collaborative atmosphere. Most of all, we are passionate about delivering innovations that improve the quality of health care and the patient experience. We are looking for like-minded individuals to join our team today! | 4/21/2023 |
| 4905 | Cambridge Isotope Laboratories Xenia, OH Quality Assurance Associate Bachelor’s Degree in chemistry or related science preferred Exp: 0-2 years |
Cambridge Isotope Separations (CIS) is searching for a GMP Quality Assurance (QA) Associate located in Xenia, Ohio. CIS is the world leader in the separation of stable isotopes and related chemistry. CIS and its parent, Cambridge Isotope Laboratories (CIL) in Massachusetts, are subsidiaries of the Otsuka Pharmaceutical Group. CIL separates both 13C and 18O at its Xenia, Ohio, facility and operates the only large capacity nongovernmental Deuterium Oxide enrichment columns in the world. We globally support a broad range of customers across many high-tech industries including pharmaceutical, semiconductor, medical diagnostic, display, and basic research. We are rapidly expanding, and the Ohio facility is an integral part of our growth for the future. Under general supervision, the primary responsibility of the QA Associate is to work as a team member to ensure and maintain the Company’s cGMP (Current Good Manufacturing Practices) compliance. | 4/21/2023 |
| 4906 | Cambridge Isotope Laboratories Andover, MA Quality Control Analyst I BS or MS degree in Chemistry, Chemistry Informatics or other relevant science degree, or relevant experience that will substitute for a formal degree Exp: One or more years |
Cambridge Isotope Laboratories, Inc. (CIL) is seeking a Quality Control Analyst I to join our team based onsite in our Andover, MA location. As the leading company in a niche scientific market, CIL works with cutting edge researchers in clinical diagnostics, metabolic research, proteomics, environmental testing, protein discovery, drug development, metabolomics, and industrial research. CIL's growing customer base spans academia, pharmaceutical and industry, enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control (QC) Analyst I is responsible for conducting routine analysis of materials under general supervision and in accordance with standard operating procedures (SOPs). The analyst will compile data for documentation of test procedures and prepare reports. They will also calibrate and maintain lab equipment. Some travel may be required to our Tewksbury, MA facility. | 4/21/2023 |
| 4907 | Janssen Pharmaceuticals San Diego, CA Neuropsychiatry Research Associate master’s degree in a relevant field Exp: 1 year |
Janssen R&D La Jolla, a member of Johnson & Johnson's Family of Companies, is recruiting a Research Associate in Neuroscience drug discovery, located in San Diego, CA. | 4/21/2023 |
| 4908 | Jnana Therapeutics Boston, MA Research Associate/Senior Research Associate, Chemical Biology BS or MS in Biology or other relevant area. Exp: 1-2 years |
Jnana Therapeutics is seeking an enthusiastic and highly motivated Research Associate/Senior Research Associate to work in our multidisciplinary Chemical Biology group. Using our novel hit generation platform and a range of cell-based assays, our research aims to unlock difficult to drug targets and ultimately small molecules that modulate these proteins. Prior experience in drug discovery is preferred. Strong commitment and good work ethic are essential. | 4/21/2023 |
| 4909 | JRF Global Audubon, PA Scientist I / Entry Level Chemist Bachelor of Science or advanced degree from an accredited college or university in chemistry or other science-related field. Exp: 1-3 years |
Set up experiments under the guidance of a Scientist II and/or Team Lead Operate equipment, observe and log the progress of experiments Promptly submit experimental data / findings to the supervisor Promptly inform the supervisor of any problems encountered during the experiments. Assist in data entry in various formats and verify accuracy of data entry Assist in writing drafts of Protocols and Reports Provide a daily update on the progress, findings and results for each experiment. Compile the data as directed by the supervisor Check the quality and accuracy of the data before submission to the supervisor | 4/21/2023 |
| 4910 | J-Star Cranbury, NJ Research Chemist Master’s Degree in Chemistry or Chemical Engineering Exp: one year |
Develop analytical methods to separate, detect, and analyze Active Pharmaceutical Ingredient (API), intermediates, impurities, starting material and excipients from drug substances and drug products. Analyze organic and inorganic compounds to determine chemical or physical properties, composition, structure, relationships, reactions, using chromatography, spectroscopy, spectrophotometry techniques including HPLC, UPLC, IC, GC, MS, UV, PXRD, DSC, TGA, NMR, and KF. Design and perform method verification and validation. Determine the specificity, linearity, accuracy, precision, forced degradation, robustness of the methods. | 4/21/2023 |
| 4911 | J-Star Cranbury, NJ Analytical Research Scientist II/III (DPD) MS in Chemistry, Pharmaceutical Science or related field. Exp: 1 -3 years |
The primary responsibility in this role is to perform analytical testing of drug substance, intermediates, drug product in support of J-Star’s drug product development projects. The incumbent should provide the expertise in characterization of drug product formulation using HPLC, GC, DSC, TGA, XRPD, dissolution apparatus, particle size analyzer, Karl Fischer titrator. Specifically, the incumbent will be responsible for analysis of formulations from preclinical through clinical formulation development, of oral solids, liquids, injectables and semi-solid dosage forms for new drug candidates. | 4/21/2023 |
| 4912 | J-Star Cranbury, NJ Research Chemist MS degree in Chemistry, Chemical Engineering or related field. Exp: 6 months |
Must have knowledge of API processing, Crystallization, Chromatography, Distillation. perform API crystallization process in compliance with cGMP and FDA regulations, utilizing analytical tools including chromatography, separation, and solvent selection; support crystallization process development by conducting studies involving compound properties and experimental conditions; participate in the scale-up development of enabling technology and experiments to facilitate the co-processing and development of API; conduct routine stability, performance, and evaluation studies for solid state characterization and pre-formulation support; support early drug crystallization process development for high potency compounds and controlled substance; purify pharmaceutical compounds using column chromatography, crystallization, trituration, extraction, and distillation; utilize experimental and simulation/modeling approaches to perform solvent selection and solve process challenges arisen from scale-up crystallization process; collect, analyze and maintain data integrity under Good Documentation Practice; write/review developmental chemistry, process optimization and process scale-up reports to support FDA requirements for CMC (Chemistry, Manufacturing and Control) sections of INDs/NDAs. | 4/21/2023 |
| 4913 | KBI Biopharma Durham, NC Upstream Process Development Associate I/II Bachelor’s in Chemical Engineering, Biotechnology or related area. Exp: 1-3+ years’ |
KBI Biopharma seeks to fill a role for Upstream Cell Culture Process Development Associate. This person will lead and assist in cell culture and harvest projects for mammalian cell lines (mainly CHO variants) in support of process development, scale-up, and technology transfer to cGMP manufacturing. | 4/21/2023 |
| 4914 | KBI Biopharma Boulder, CO Manufacturing Associate I/II (Nights) Bachelor’s degree Exp: 0-5 years |
This position will be on a 4-3 night shift schedule. The hours are 7:00 pm to 7:00 am. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels | 4/21/2023 |
| 4915 | KBI Biopharma Boulder, CO Manufacturing Associate I/II (Nights) Bachelor’s degree Exp: 0-5 years |
This position will be on a 2-2-3 night shift schedule. The hours are 7:00 pm to 7:00 am. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels | 4/21/2023 |
| 4916 | KBI Biopharma Durham, NC Downstream Process Development Associate I/II or Senior For PD Associate I: B.S. degree in biotechnology or related area; For PD Associate II: M.S. degree (industrial experience a plus). Exp: B.S.: 0-2+ years’; M.S.: 0-2+years’ |
Responsible for supporting process development activities for downstream production processes, instruments, and equipment. | 4/21/2023 |
| 4917 | KBI Biopharma Durham, NC Research Associate I/II For RA I: Bachelor’s degree in chemistry, biochemistry or related area; For RA II: Master’s degree in chemistry, biochemistry or related area. Exp: RA I: 0+ years’; RA II: 0+ years’ |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 4/21/2023 |
| 4918 | Dropworks Hercules, CA Production Chemist I - Temporary - $1,500 Hiring Bonus Bachelor’s degree in a life science or related field. Exp: 1-3 years |
Contribute to our mission of improving the quality of life for millions by contributing to the production of life science products our customers use to advance healthcare. Help build high quality products following detailed processes and procedures to ensure the integrity of our products. | 4/9/2023 |
| 4919 | Dr. Reddy's Laboratories Middleburgh, NY Associate Quality Bachelor’s Degree in Chemistry or Biochemistry is normally required. Exp: 0-3 year's |
We seek a dynamic Quality Associate to join our fast-paced environment at our Manufacturing site in Middleburgh, NY | 4/9/2023 |
| 4920 | EAG Laboratories Minneapolis, MN Laboratory Technologist l Bachelor’s degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Technologist I responsibilities include, but are not limited to, the following: Following prescribed procedureswhile performing serology testing on donor plasma and serum including EIA, PCR, and ABO blood typing. Calculating the results of the tests performed as necessary Operating, calibrating, conducting performance checks, and maintaining laboratory analyzers and equipment Recognizing and correcting basic analyzer malfunctions. Notifying management personnel when appropriate Preparing reagents or media from a prescribed procedure Evaluating media, reagents, and calibrators according to established criteria Conducting established quality control procedures on analytical tests, equipment, reagents, media, and products Evaluating results of quality control and implementing corrective action when indicated Determining performance specifications for new methods Confirming and verifying results through knowledge of techniques, principles, and analyzers Monitoring quality assurance/continuous improvement programs | 4/9/2023 |
| 4921 | EAG Laboratories Minneapolis, MN Technologist l (3rd Shift) Bachelor’s degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Technologist I responsibilities include, but are not limited to, the following: Following prescribed procedures while performing serology testing on donor plasma and serum including EIA, PCR, and ABO blood typing. Calculating the results of the tests performed as necessary Operating, calibrating, conducting performance checks, and maintaining laboratory analyzers and equipment Recognizing and correcting basic analyzer malfunctions. Notifying management personnel when appropriate Preparing reagents or media from a prescribed procedure Evaluating media, reagents, and calibrators according to established criteria Conducting established quality control procedures on analytical tests, equipment, reagents, media, and products Evaluating results of quality control and implementing corrective action when indicated Determining performance specifications for new methods | 4/9/2023 |
| 4922 | EAG Laboratories St. Louis, MO Laboratory Technician (Analytical Chemistry) - EAG Laboratories - St. Louis, MO BS degree in Chemistry. Exp: 1-3 years |
EAG is actively seeking a Lab Technician to support Analyst and Scientist in the formulation of industrial and consumer products. In this position, you will be responsible for: Performing sample preparation. Assist with recording test data providing some basic analysis and interpretations. Maintaining specified records of scientific data. Protecting confidential information and proprietary processes. Handling customer materials and company equipment in a responsible and efficient manner. | 4/9/2023 |
| 4923 | EAG Laboratories St. Louis, MO Analyst, Analytical Chemistry - EAG Laboratories MS degree in Chemistry. Exp: 0-2 years |
EAG is actively seeking a chemist to assist in the formulation of industrial and consumer products. In this position, you will be responsible for: Applying standard and non-standard techniques, procedures and criteria to carry out a sequence of related tasks to determine the composition, properties and/or structure of materials. Performing sample preparation. Recording test data providing some basic analysis and interpretations. Maintaining specified records of scientific data. Preparing reports on analytical results for customers. Protecting confidential information and proprietary processes. Handling customer materials and company equipment in a responsible and efficient manner. | 4/9/2023 |
| 4924 | EAG Laboratories Phoenix, AZ Bacteriology / Biochemistry Analyst - Eurofins EmLabs Bachelor’s degree in microbiology, molecular biology, biochemistry or a closely related science. REQUIRED Exp: 1-2 years |
The Analyst performs bacteriological and molecular/biochemical analysis on samples including but not limited to aerobiological, environmental and drinking water. The Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 4/10/2023 |
| 4925 | EAG Laboratories Phoenix, AZ Analyst I - Eurofins Built Environment - Phoenix, AZ BS or BA in a closely related science. Exp: 1-2 years |
Eurofins Built Environment Testing is searching for a Fungal Analyst in Phoenix, AZ. The Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation | 4/10/2023 |
| 4926 | Exponential Business & Technologies Eden Prarie, MN Nano Analytical and Testing Lab Technician BE or BS degree in Materials Science and Engineering, Mechanical Engineering, Physics, Chemistry or related disciplines. Exp: One to two years |
Ebatco is seeking an energetic, self-disciplined, customer service oriented technical person to join its Nano Analytical and Testing Laboratory (NAT Lab). As a technical member of the NAT Lab team, the technician performs contract lab services and instrument demonstrations with appropriate levels of support and supervision, operates advanced nano/micro scale scientific instruments, collects testing and measurement data, and writes technical report on experimental results and observations. | 4/10/2023 |
| 4927 | Elektrofi Boston, MA Analytical Development - Associate Scientist Bachelor's or Master's degree in Microbiology or a related field. Exp: 0-2 years |
Elektrofi is seeking a highly motivated and detail-oriented Associate Scientist who will be responsible for developing, qualifying and performing microbiological and sterility assays for release testing our drug products. This individual will join a multidisciplinary team of scientists and engineers and contribute to a variety of CMC activities in a highly collaborative environment. | 4/10/2023 |
| 4928 | Elektrofi Boston, MA Formulation Development - Associate Scientist BS in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biology, Bioengineering, or a related field. Exp: 0-2 years |
Elektrofi is looking for an Associate Scientist to support a team responsible for the development of platform formulations for Elektrofi’s proprietary microparticle production process. The candidate will support ongoing activities towards the development of Elektrofi’s biologics formulation platform. This individual will join an early-stage, multidisciplinary team of scientists and contribute to a variety of formulations activities in a highly collaborative environment. | 4/10/2023 |
| 4929 | Elektrofi Boston, MA Internal Manufacturing - Engineer I/II B.S. in Mechanical, Chemical, Biomedical, or Materials Engineering, Chemistry, Physics, or a related engineering discipline. Exp: up to 2 years’ |
Elektrofi is looking for an Engineer I/II to support manufacturing, process development, or drug product development in the manufacturing and analysis of biologically active microparticle suspensions and their interactions with delivery devices. This individual will join a growing, multidisciplinary team of scientists and engineers and contribute to a variety of manufacturing and process development activities in a highly collaborative environment. | 4/10/2023 |
| 4930 | Elektrofi Boston, MA Analytical Development - Associate Scientist Bachelor's or Master's degree in Microbiology or a related field. Exp: 0-2 years |
Elektrofi is seeking a highly motivated and detail-oriented Associate Scientist who will be responsible for developing, qualifying and performing microbiological and sterility assays for release testing our drug products. This individual will join a multidisciplinary team of scientists and engineers and contribute to a variety of CMC activities in a highly collaborative environment. | 4/10/2023 |
| 4931 | Elektrofi FLOOR 2, MA Drug Product Innovation - Associate Scientist/Engineer BS Degree in Chemical, Biomedical, Materials, or Pharmaceutical Engineering, or Colloid Science or relevant discipline. Preference for MS in relevant Exp: 0-3 years’ |
Elektrofi is looking for an Associate Scientist or Engineer I to support the Drug Product Innovation team and investigate Elektrofi’ s microparticle suspensions. This work includes phase appropriate container selection, determination of microparticle and suspension critical quality attributes (CQAs), optimization of resuspendability and injectability, fill-finish development, as well as the development of new embodiments of the product across a range of applications. An exciting opportunity to join a multidisciplinary team of scientists and engineers and contribute to a variety of research and development activities in a highly collaborative environment. | 4/10/2023 |
| 4932 | EMD Serono Rockville, MD Associate Scientist 2 - 2nd Shift Bachelor’s Degree in a scientific discipline (e.g., Biology, Chemistry, Microbiology, etc. ). Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist 2 – 2nd Shift , you will perform assays and safety testing required to manufacture clinical and commercial products. You will make scientific observations, maintain detailed workbooks/documentation, and ensure all documentation fulfills generally accepted professional/industry standards. | 4/10/2023 |
| 4933 | EMD Serono Carlsbad, CA Mechanical Engineer Bachelor’s Degree in Mechanical Engineering, Chemical Engineering, or any engineering discipline. Exp: 1+ years |
The Mechanical Engineer develops new processes for ultra-high purity (UHP) applications in the technologically advanced semiconductor industry (SEMI). You will be part of a small team of engineers and technicians working to develop new products that will package ultra-high purity chemicals meeting rigorous quality and performance requirements. The position will be focused on developing new processes to improve the quality of the products and performing root cause analysis of problems. While the broader company is strongly focused on chemistry, this role is focused on the relevant mechanical aspects. | 4/10/2023 |
| 4934 | EMD Serono Carlsbad, CA Quality Analyst I - Microbiology Bachelor’s Degree in science, Chemistry, Biology, or a similar life science discipline Exp: 1+ years |
As a Quality Analyst I in the Quality Control Environmental Monitoring group, you will support the site by testing the quality of the cleanroom manufacturing environment and ensuring that SAFC Carlsbad adheres to strict regulatory and ISO requirements. Monitoring activities include but are not limited to, collecting surface, air, water, and personnel samples, monitoring manufacturing processes, enumerating microbial plates, data entry, trend analysis, reporting deviations and nonconformances, and investigation support. The role will entail operating in a fast-paced, highly dynamic environment in collaboration with other departments as well as external stakeholders. This role will support the daily operations of the Environmental Monitoring Group, collect samples, process samples, complete documentation, enter data, and review data for Environmental monitoring. | 4/10/2023 |
| 4935 | EMD Serono Carlsbad, CA Specialist II, Analytical Development Master’s Science Degree in chemistry, biochemistry, biology, or other life science studies. Exp: 6 months |
MilliporeSigma is seeking a motivated Specialist II to join its dynamic and collaborative Process and Analytical Development team at the Carlsbad viral vector CDMO facility. The successful candidate will contribute to the development and execution of analytical assays for innovative viral vector therapeutics. | 4/10/2023 |
| 4936 | EMD Serono Sheboygan Falls, WI Quality Assurance Associate Bachelor's Degree in Chemistry, Biology, Healthcare, or other Life Science discipline. Exp: 1+ years |
The Quality Assurance Associate at MilliporeSigma in Sheboygan Falls, WI, will support quality systems, and ensure their alignment with business goals, premier customer expectations and requirements, as well as global business unit best practices. The Associate will establish strong collaborative relationships with all departments within the organization and will deliver on quality and regulatory commitments, working autonomously to effectively manage delivery of results within targeted deadlines. | 4/10/2023 |
| 4937 | EMD Serono Sheboygan Falls, WI Associate Quality Control Chemist (Laboratory) B.S. or B.A. Degree in chemistry, biochemistry,?chemical engineering or other life science discipline. Exp: 1+ years |
Evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Hours: 4:30 PM - 2:30 AM, Wed – Sa | 4/10/2023 |
| 4938 | Millipore Rockville, MD Associate Scientist 1 Bachelor’s Degree in a scientific field (i.e., Biology, Chemistry, etc.) Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist 1, your activities will support assay development through commercial application of new and innovative service offerings within the biosafety testing space. You are responsible for the scientific integrity of technical work performed in the laboratory, and will make scientific observations, maintain detailed workbooks/documentation, and ensure all documentation fulfills generally accepted professional/industry standards. Hours Monday-Friday 12:00pm-8:00pm | 4/11/2023 |
| 4939 | Millipore Kankakee, IL Quality Control Scientist Bachelor’s degree in Biology, Chemistry, or another related life science discipline. Exp: 1+ years |
At MilliporeSigma, the Quality Control Scientist is responsible for performing multi-discipline analytical test methods for a variety of product lines to help achieve overall business objectives. This role is also responsible for maintaining the Product Stability, Product Retention, and Reverse Osmosis Water Quality Programs in accordance with the current regulatory guidelines. Additionally, this role supports Special Projects and Process Engineering analytical requirements to maintain existing, and future, business development. | 4/11/2023 |
| 4940 | Millipore Carlsbad, CA Quality Analyst II, Microbiology Bachelor’s Degree in science, Chemistry, Biology or similar life science discipline. Exp: 1+ years |
As a Quality Analyst II in the Quality Control Microbiology group, you will support the site by performing environmental monitoring of the cleanroom manufacturing environment as well as microbiological testing of pharmaceutical grade water systems, raw materials, and production samples. Environmental Monitoring responsibilities include, but are not limited to, collecting surface, air, water, and personnel samples, monitoring manufacturing processes, enumerating microbial plates, data entry, trend analysis, reporting deviations and nonconformances, and investigation support. Laboratory Testing responsibilities include, but are not limited to, bioburden testing, endotoxin testing, media fill testing, growth promotion testing, and biological indicator testing. The Carlsbad Viral Vector Manufacturing Facilities are a CDTMO focused on viral vectors and gene therapies. The role will entail operating in a fast-paced, highly dynamic environment in collaboration with other departments as well as external stakeholders. A role in Quality Control offers the opportunity to work with and learn about all the different aspects of the organization, from Facilities to Validation to Manufacturing and Quality Assurance. | 4/11/2023 |
| 4941 | Millipore Jaffrey, NH QC Supervisor, Physical Test Lab Master’s Degree or higher-level education in Chemistry, Chemical Engineering, Biochemistry, or Biology Exp: 1+ years |
As a Quality Supervisor at MilliporeSigma in Jaffrey NH, you will be supervising and supporting a laboratory group of personnel and resources for QC Labs. A Shift: Monday - Friday 8 AM - 5 PM | 4/11/2023 |
| 4942 | Millipore St. Louis, MO GMP Engineering And Maintenance Compliance Associate Bachelor’s degree in Engineering Exp: 1+ years |
MilliporeSigma has an exciting opening at their Cherokee/St. Louis site. The Engineering and Maintenance Compliance Specialist's primary role is to provide support to the cGMP operations. This position will be responsible for assisting Engineering, Manufacturing, Technical Operations, and QA with quality support as it relates to change control, equipment non-conformances, process deviations, routine equipment system maintenance and Building Management System support. Additional responsibilities may include on the floor oversight during manufacturing, incident investigations and resolution, monitoring of the building management system. | 4/11/2023 |
| 4943 | Millipore St. Louis, MO Research And Development Scientist Master’s degree in a scientific discipline Exp: 1+ year |
Your Role: Design and implement experimental plans and procedures. Responsible for the scientific integrity of technical work performed in the laboratory and maintain detailed workbooks and documentation. The purpose of this position is to support R&D efforts for designing new products and/or platform technologies. Incumbent will assist in development and commercialization of new product offerings by developing and executing a broad range of protocols. This position is located at the Laclede Avenue location. | 4/11/2023 |
| 4944 | Endo Pharmaceuticals Rochester, MI Quality Associate Specialist, Product Release - Afternoon Shift BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 4/11/2023 |
| 4945 | Endo Pharmaceuticals Rochester, MI Quality Associate Specialist, Product Release - Midnight Shift BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 4/11/2023 |
| 4946 | Entrada Therapeutics Boston, MA Research Associate, Process Chemistry CONTRACT Bachelors and/or masters in biochemistry, chemistry, chemical, or biological engineering, or a related discipline. Exp: 0‑2 years |
The Opportunity Routinely support operation of large-scale solid-phase reactors Learn the workflows of technical teams by shadowing lab scientists Identify and/or optimize operations to improve process robustness, throughput, and cost while maintaining product quality Assist with data management and assay analysis Works towards future scalability Provide mentorship to peers work toward an efficiently cross trained team | 4/12/2023 |
| 4947 | Federation Bio South San Francisco, CA Research Associate I Bachelor of Science degree in a Life Sciences discipline. Exp: (1) year |
We are seeking an individual to play a key role in our team in supporting critical research and IND-enabling animal studies. A successful candidate is required to have prior animal husbandry experience and proficiency in rodent biomethods. This role will be responsible for day-to-day maintenance of the animal vivarium where germ-free, gnotobiotic, and specific-pathogen free mice are maintained. The ideal candidate will need to demonstrate aptitudes in foresight, planning and ability to organize and schedule the many tasks associated with running an animal facility. The candidate should be flexible, excited to wear the many hats to meet the dynamic needs of a start-up environment, proactive and positive. This person should also have the desire to contribute to a vibrant and dynamic culture. Some ability to build and assemble equipment is desired. Understanding the principles of sterilization is an integral component of this position. Must have the ability to lift 50 pounds and stand for extended periods of time. Some work on weekends may be required. This position will report to Federation Bio’s head of in vivo sciences. This is an in-person position and located in South San Francisco, CA. | 4/13/2023 |
| 4948 | Forge Biologics Columbus, OH Associate Scientist/Senior Associate Scientist, Process Development - Upstream Master’s degree in Biology, Chemistry, or relevant area. Exp: 0+ years |
We are currently seeking an Associate Scientist/Senior Associate Scientist, Process Development - Upstream to join the Forge Biologics team. This is an exciting opportunity to assist in the execution of laboratory experiments and protocols for upstream process development efforts. The candidate will assist in process development protocols/studies to optimize procedures for unique viral vector platform process and to assist in the transfer of client programs. The Associate Scientist/Senior Associate Scientist will work to meet production goals, notify management of any potential delays in the schedule, and make recommendations to resolve the issues. This position reports to the Scientist II, Process Development - Upstream and is responsible for laboratory stocking, inventory management, and assisting in laboratory activities. This includes preparing growth media, chemical buffers, solutions or other reagents that involve the mixing of subcomponents and preparing raw materials for use in production steps. Work activities may also include performing laboratory techniques (cell culture, vector purification) in support of production of viral vectors. It is expected that this individual will work as a member of the development team while accomplishing the timely completion of assignments and reporting of unexpected technical issues. | 4/13/2023 |
| 4949 | FORMA Therapeutics West Lebanon, NH Cell Therapy Associate Master’s Degree in Cell Biology, Molecular Biology or a closely related field. Exp: one (1) year |
This position has the responsibility of working with senior level Scientists and manufacturing associates to execute process development, scale-up, tech transfers, and validation studies in support of manufacturing or analytics. Additionally, the role will necessitate experimental troubleshooting, GMP documentation and laboratory investigations. The position will require understanding the underlying science of the process and manufacturing equipment, or assay methods and instruments. | 4/13/2023 |
| 4950 | FORMA Therapeutics Clayton, NC Quality Control Analyst I or II BA/BS in a science or related field of study Exp: one (1) year |
Perform & review analysis of in-process, release & stability samples of API &/or filled product in accordance with cGMP, site & corporate procedures & policies. Transfer of technology & processes in accordance with relevant project plans & timelines. This is a Quality Control chemistry laboratory group focusing on incoming raw materials. | 4/13/2023 |
| 4951 | FORMA Therapeutics Clayton, NC Quality Control Analyst I or II BA/BS in a science or related field of study Exp: one (1) year |
Perform & review analysis of in-process, release & stability samples of API &/or filled product in accordance with cGMP, site & corporate procedures & policies. Transfer of technology & processes in accordance with relevant project plans & timelines. | 4/13/2023 |
| 4952 | FORMA Therapeutics West Lebanon, NH Quality Control Microbiologist (Sr. Level Experience Preferred) Bachelor’s degree in a scientific discipline or equivalent. Exp: zero (0) to two (2) years |
This position carries out routine microbiological testing to support the manufacturing facility. All work is carried out in a QC GMP environment where the highest level of compliance and attention to detail is necessary. Role focuses on routine activities such as utility and facility monitoring, data reporting, general laboratory support and activity coordination. This individual works with supervision/instruction on routine work and detailed instruction for new activities. This position schedule is Tuesday-Saturday from 8:00am-5:00pm. | 4/13/2023 |
| 4953 | FORMA Therapeutics West Lebanon, NH Manufacturing Science and Analytical Technology Associate I Bachelor’s degree or equivalent in Biochemistry, Chemistry, Engineering or a closely related field. Exp: one year |
This position has the responsibility of working with senior level Scientists to execute laboratory scale process development or validation studies in support of process or assay development, or process troubleshooting or scale-up. The scientific knowledge in this position will range from familiarity with details of manufacturing process, process chemistries, development studies and relevant assay methods and instruments. This position will be one of the interfaces between MSAT and Manufacturing or Quality. | 4/13/2023 |
| 4954 | FORMA Therapeutics West Lebanon, NH Manufacturing Technician (Levels I-IV) Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. Our Manufacturing Technicians work 12-hour shifts and we offer the following schedules: Day Shift (7am-7pm) Sunday-Tuesday and everyother Wednesday Thursday-Saturday and everyother Wednesday Night Shift (7pm-7am): Sunday-Tuesday and everyother Saturday Wednesday-Friday and everyother Saturday | 4/13/2023 |
| 4955 | Frenova Renal Research Lawrence, MA Mechanical Engineer I Bachelor's Degree in related Engineering or scientific discipline required Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 4/14/2023 |
| 4956 | Frenova Renal Research Ogden, UT R & D Engineer I - Dialyzers Bachelor's Degree in related Engineering or scientific discipline required Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 4/14/2023 |
| 4957 | Frenova Renal Research Southhaven, MS Medical Lab Scientist - Trace Bachelor’s Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 – 3 years’ |
Now offering a $2,000 sign on bonus PURPOSE AND SCOPE: Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 4/14/2023 |
| 4958 | Catalent Greenville, NC Analytical Chemist I Bachelor’s degree a science-related discipline (e.g. Biology, Chemistry, Pharmaceutical Sciences). Exp: 0+ years |
Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. The Analytical Chemist I primarily performs routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. | 4/5/2023 |
| 4959 | Catalent Morrisville, NC Associate Scientist Master’s degree Exp: 0 years |
Catalent Pharma Solutions is Morrisville, NC is hiring an Associate Scientist for the Laboratory Group. The laboratory groups at Catalent RTP are responsible for the support of pharmaceutical product development in a range of dosage forms both directly with customers and in collaboration with other Catalent facilities. This includes formulation development, structural chemistry, analytical support, and clinical trials material manufacturing. | 4/5/2023 |
| 4960 | Catalent St. Petersburg, FL Associate Scientist II, Quality Control Requires BS or BA with college course work in related sciences, analytical laboratory experience preferred but not required. Exp: 0 years |
The Associate Scientist II, Quality Control will Independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines. Communicate results in written and oral presentations. Help in writing Procedures, Specifications and Test Methods. Keep abreast of literature in field; help train colleagues; contribute to continuous improvement within the group. Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. Maintain proper records in accordance with all SOP's and policies. | 4/5/2023 |
| 4961 | Catalent St. Petersburg, FL Associate Scientist II Requires BS with college course work in related sciences. Analytical laboratory experience preferred not required. Exp: 0 years |
The Associate Scientist II, Quality Control will Independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines. Communicate results in written and oral presentations. Help in writing Procedures, Specifications and Test Methods. Keep abreast of literature in field; help train colleagues; contribute to continuous improvement within the group. Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. Maintain proper records in accordance with all SOP's and policies. | 4/5/2023 |
| 4962 | Catalent Kansas City, MO Quality Control Associate Scientist II Bachelor's degree in related life science or physical science field. Exp: 0+ years |
Catalent Pharma Solutions in Kansas City, MO is hiring a Quality Control Associate Scientist II. The Quality Control Associate Scientist II under close supervision and guidance, performs tasks from detailed instructions and established procedures. Comply with site SXPs, corporate policies, and Environmental Health and Safety requirements. Has basic knowledge of the principles and concepts of discipline (e.g. Biology, Chemistry). Applies technical skills to complete assigned work within own group/project team. A self-motivated, detail-oriented person who is able to make decisions and solve problems is essential. Able to work independently with little to no supervision, and flexible to also assist team members as needed. | 4/5/2023 |
| 4963 | Catalent Kansas City, MO Pharmaceutical Development Associate Scientist II Bachelor's degree in related life science or physical science field is required. Exp: 0+ years |
Catalent Pharma Solutions in Kansas City, MO is hiring a Pharmaceutical Development Associate Scientist II. The Kansas City Pharmaceutical Development Associate Scientist II supports formulation/process design and development of oral solid dosage forms. Participates/leads in clinical trial manufacturing endeavors and ensures that all work is carried out in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs) | 4/5/2023 |
| 4964 | Catalog Charlestown, MA Associate Process Engineer- DNA Synthesis A BS in mechanical or biochemical engineering. Exp: 1-2 years |
CATALOG is a rapidly expanding, Boston-based start-up on a mission to enable new paradigms for data preservation and computation. We are looking for a motivated entry-level engineer eager to work with an interdisciplinary team of biologists, engineers, and computer scientists. You will be responsible for routine operation and maintenance of our proprietary high throughput DNA writing system, used to build vast sets of information-encoding synthetic DNA molecules. As part of our rapidly expanding group, you will help to build, optimize, and evaluate molecular datasets at a scale enabling novel applications for the world’s first DNA storage and computing platform. | 4/5/2023 |
| 4965 | Catalog Charlestown, MA Research Associate, Molecular Biology MS in biochemistry, molecular/synthetic biology or a related field. Exp: 0 years |
CATALOG is a well-funded, rapidly expanding, Boston-based start -up on a mission to preserve and compute on the world’s most valuable data. We are growing our team to build CATALOG’s DNA-based data storage and computation platform. We are looking for a motivated Scientist with a background in synthetic biology to join our interdisciplinary team of biologists, engineers, and computer scientists to design novel storage and computing architectures and translate them into scalable read/write operations. As part of the newly established Future Technologies group, you will help to build and evaluate novel synthetic biology strategies that help realize the world’s first DNA storage and computing platform. | 4/5/2023 |
| 4966 | Cayman Chemical Ann Arbor, MI Associate Scientist - NMR Specialist Master’s degree in chemistry or related field. Exp: none (with Master’s degree) |
Responsibilities and Duties: Apply knowledge of NMR spectroscopy to support structure elucidation of Cayman’s research chemicals Operate and maintain NMR and MS instrumentation Process and interpret NMR spectra for entry into a spectral database Collaborate with quality control to perform and evaluate NMR testing on catalog products Perform routine NMR maintenance including cryogen fills, shim optimization, and pulse width calibration Work with supervisor and manager to align priorities to Analytical Chemistry Division goals Substantively contribute to regular group, project team, and departmental meetings Assist with general upkeep of the NMR lab | 4/5/2023 |
| 4967 | Cisbio San Diego, CA Research Associate - Antibody Development Bachelor of Science with a discipline in cell biology, immunology, and biochemistry preferred. Exp: 1-2 yrs |
This person would be responsible for developing phosphosite specific monoclonal antibodies in BioLegend derived from immunized animals by performing antigen preparation, host immunization, bleed analysis, and cell lysate preparation. Techniques involved in this job include antigen formulation, animal immunization and tissue harvesting, cell culture and antibody analysis using ELISA and Western blot techniques. | 4/5/2023 |
| 4968 | Cisbio San Diego, CA Research Associate - Exploratory R&D B. S. or M.S. in Biology, Immunology or another related field. Exp: 1 year |
The Research Assistant will be involved in product development and optimization of cell culture process and new product development. In particular, he/she will be involved in determining the feasibility of new products and new cell culture processes for in-house and custom projects. This role will also be involved in troubleshooting issues associated with cell culture. This role requires mammalian cell culture experience. Knowledge of process development for antibody production, particularly hybridoma, on a small and large scale is a plus. He/she must have excellent organizational skills, attention to detail, and accuracy. Be able to maintain good documentation practices and generate reports. Must be proficient in computer software use (Excel, Word, and PowerPoint). Must be self-motivated and able to multi-task. Must be collaborative and have good communication skills. | 4/5/2023 |
| 4969 | Cisbio San Diego, CA Research Associate - Recombinant Protein & Molecular Cloning BS in biological sciences. Exp: 1 year |
This position is responsible for developing cutting edge recombinant protein research products in Molecular Cellular Biology group. The research associate will be involved on developing a new line of recombinant protein products by supporting other team members. The duties include preparing buffer solutions and cell culture media, performing PCR and DNA purification according to standard operating procedures, performing bacterial and mammalian cells cultures, and purifying recombinant proteins with affinity tag. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 4/5/2023 |
| 4970 | Cisbio Pittsburgh, PA Molecular Laboratory Technologist Bachelor's degree in biology or related scientific discipline. Exp: 0-2+ years |
Performs clinical genetic laboratory tests, procedures and analysis to provide data for diagnosis, treatment, and prevention of disease in adults, children, and newborns. | 4/5/2023 |
| 4971 | Cognate Biosciences Rockville, MD Biomanufacturing Associate I Bachelors degree in biology/life sciences, bioengineering, or related discipline. Exp: 0-1 year |
The Biomanufacturing Associate I will play an integral role within CRL’s gene therapy manufacturing function by understanding and applying biological, bioprocess, manufacturing, and mechanical principles, processes, procedures, inputs, and outputs, for designated production processes and handovers, within a cGMP and GLP environment. This will ensure the timely production and release of quality products, based on client specifications. This role will perform a range of routine and semi-routine tasks, some of which are moderately difficult, requiring judgment in resolving issues or making recommendations, with guidance as needed, in order to proficiently execute manufacturing protocols in a regulated environment. | 4/5/2023 |
| 4972 | Cognate Biosciences Cleveland, OH Research Analyst I Bioanalytical Chemistry Bachelor’s degree (BA/BS) or equivalent experience. Exp: 0 year |
We are seeking a Reseach Analyst 1- Bioanalytical Chemistry for our Safety Assessment CRL Site located in Cleveland, OH. | 4/5/2023 |
| 4973 | Cognate Biosciences Spencerville, OH Research Technician I BA/BS in a life science field preferred. Exp: 0-6 months |
We are seeking an experienced Research Technician Assistant for our Toxicology Team located in Spencerville, OH. Do you have experience working with animals? 4H? FFA? Vet Assistant? Farm/AG? Or a medical background working in hospitals/STNA/EMT? This could be a great fit for you. A Research Technician Assistant is responsible for: collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Hourly Rates $18-$19/hr. $1000 Sign on Bonus. 3 weeks vacation and additional sick time. | 4/5/2023 |
| 4974 | Cognate Biosciences Shrewsbury, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months to 1 year |
Charles River Laboratories is seeking an Research Technician I for our InVivo (InLife) Team within our Safety Assessment site located in Shrewsbury, MA. The Research Technician 1 will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 4/5/2023 |
| 4975 | Cognate Biosciences Rockville, MD Bioprocess Engineer I B.S. in Chemical Engineering, Bioengineering, Chemistry, Biochemistry, or related subject area. Exp: 1 – 4 years |
The Bioprocess Engineer I is responsible for the accurate and timely scale up of process development data to large scale manufacturing. This responsibility includes scale up, document authorship, process data tracking, deviation investigation, and data analysis to ensure right-first-time clinical and commercial manufacturing and continuous improvement. This position interacts with Process Development, Manufacturing, Facilities, Quality Control, Quality Assurance, and Supply Chain to ensure project success. | 4/5/2023 |
| 4976 | Cognate Biosciences Newark, DE Research Associate Bachelor's degree (B.A./B.S.) or equivalent in Microbiology or Molecular biology or related scientific field. Exp: 1 to 2 years |
The Microbial Solutions team located in Newark, DE is seeking a Research Associate. This role will be responsible for assisting with experimental design, performing experiments and analyzing data to support new product and service development and associated support functions related to Research and Development within Microbial Solutions. | 4/5/2023 |
| 4977 | CooperSurgical Tucson, AZ Technician I - Quality Control Bachelor’s degree in one of the biological, chemical, or physical sciences. Exp: 0 - 1 year |
Cord Blood Registry (Cbr) Technician I - Quality Control is responsible for analyzing and documenting test results from our cord blood and cord tissue processed samples, releasing raw materials, supporting the analytical and processing equipment maintenance program, conducting environmental monitoring, and providing a wide range of critical functions that support the cryogenic storage of our client’s final product. This position is also responsible for providing our internal customers with technical expertise while maintaining the highest quality services possible | 4/6/2023 |
| 4978 | CordenPharma Boulder, CO QC Analyst - Nights Bachelor's Degree (BA) from 4-year college or university. Exp: 0-1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training Manual. Maintains a high level of housekeeping and attention to detail. | 4/7/2023 |
| 4979 | CordenPharma Boulder, CO Night - Standards and Stability Analytical Chemist Bachelor's degree (BA) from a 4-year college or university. Exp: 0-1 year |
This is the intermediate level technical professional within the R&D Team. Performs analytical tasks accurately and efficiently without supervision, to qualify standards, support the Stability Program, and support on-going development projects. | 4/7/2023 |
| 4980 | Contract Pharmacal Hauppauge, NY Chemist (Quality Control) Bachelor’s degree in Chemistry or related science required. Exp: 1-9 years |
The Chemist, QC position is responsible for and has experience in performing chemical testing and completion of real-time documentation per cGMPs and current SOPs. | 4/7/2023 |
| 4981 | Culture Biosciences South San Francisco, CA Bioprocess Associate, Cell Culture Bachelor’s degree in Biology, Microbiology, Chemical Engineering, Biotechnology or a science related background. Exp: 1-2 years |
We are looking for a Bioprocess Associate, with experience in bioreactors and mammalian cell culture, to join our bioreactor operations team. Your work will contribute to getting novel biotechnology products to market faster and more efficiently. Your job will be to work as part of a team of bioprocess associates, engineers and project leads to execute customer projects and build an efficient operations department. In particular, you will learn mammalian cell culture techniques and work with in-house custom built software and equipment designed for bioreactor operations. | 4/7/2023 |
| 4982 | Cytovance Biologics Oklahoma City, OK QC Stability Associate QC Stability Associate B.S. in Life Sciences/Chemistry Exp: 1-3 years |
The Stability Associate will participate in the QC Stability Study Program activities which includes designing and drafting stability study protocols according to ICH guidance for drug substance, drug product and reference standard, participate in range of quality control analytical activities such as analytical assay performance, and transfer of standard protein characterization methods. Duties will be carried out in accordance with quality standards and procedures set by the company and applicable government agencies | 4/7/2023 |
| 4983 | Cytrellis Biosystems Woburn, MA Mechanical Engineer Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or equivalent job experience. Exp: 0 – 3 years |
The Mechanical Engineer is responsible for the mechanical design and development of our future product platforms in a highly collaborative environment. The Mechanical Engineer develops a thorough understanding of the product technology, leads the mechanical development of next generation devices, and demonstrates technical feasibility through analysis and testing. The position may be required to perform all, or a combination of the following essential responsibilities as determined by necessity. This role is located at the Company’s Woburn, MA office. | 4/7/2023 |
| 4984 | Day Zero Diagnostics Boston, MA Lab Research Associate II / Senior Research Associate Bachelor's Degree in molecular biology, biochemistry or microbiology from a four-year college/university. Exp: 1-2 years |
The Lab Research Associate II/ Senior RA will work closely with an interdisciplinary team of scientists, RAs, and engineers to test and optimize our diagnostic workflows to support DZD’s efforts to develop a commercial diagnostic device. | 4/7/2023 |
| 4985 | Dendreon Seal Beach, CA TEMP-HIRE Manufacturing Operations Associate BA/BS degree in Science. Exp: 0 years |
Aseptic manufacturing and assembly of clinical and commercial human blood derived components in a clean-room environment (Class 10,000/ISO7, and Class 100,000/ISO8). | 4/7/2023 |
| 4986 | DiaCarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science is a plus. Exp: 0-1 year |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 4/7/2023 |
| 4987 | DiaCarta Pleasanton, CA Research Associate S. degree in molecular biology or a related field Exp: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 4/7/2023 |
| 4988 | DiaCarta Pleasanton, CA Manufacture Technician S. degree in Molecular Biology, Cell Biology, Biotechnology or related field Exp: 1-year |
This position is a member of a fast-paced production team and will be responsible for the following tasks. Purchase raw materials from a vendor Receive incoming materials and perform inspection and inventory recording Production of DiaCarta IVD products to meet sales demands Labeling of raw materials and finished goods Perform calibration or preventative maintenance of the instrument Participate in process improvement projects Compliance with corporate quality systems Other on-the-job assignments indicated by management | 4/7/2023 |
| 4989 | Dice Therapeutics South San Francisco, CA Research Associate / Senior Research Associate in Medicinal Chemistry BS or MS in organic chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based synthetic chemistry Research Associate / Senior Research Associate to join our medicinal chemistry team. This individual will be a key contributor to the synthesis of intermediates and final compounds within the goals of developing treatments for inflammatory diseases. Must have legal right to work in US. | 4/7/2023 |
| 4990 | DiscGenics Salt Lake City , UT QA/QC Analyst I Bachelor’s degree in the Biological Sciences, or related field. Exp: 1 year |
This is a hybrid role with responsibilities for QA and QC, depending on the needs of DiscGenics as we grow. The Analyst I, QA/QC is responsible for supporting functional leaders and managers to establish and grow Quality related documentation and processes reporting directly to the Manager, Quality Assurance. The Analyst I, QA/QC Provides guidance on quality assurance initiatives to ensure that operations remain in a state of compliance with applicable regulations for biologics including cell therapies. This role interacts with all levels of the organization. Delivers collaborative and positive leadership to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. | 4/7/2023 |
| 4991 | Distributed Bio Mattawan, MI Research Analyst I- Formulations Bachelor’s/Master’s degree in a relevant field. Exp: 0 year |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. The pay range for this position is $23/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. The shift is for the weekend, Friday to Monday 6 AM-2:30 PM but will train for the first 12 weeks Monday-Friday 6 AM-2:30 PM. When you work Saturday or Sunday there will be a 10% shift differential. | 4/7/2023 |
| 4992 | Distributed Bio South San Francisco, CA Research Study Technician I Bachelor's (B.A./B.S.) Degree preferred. Exp: 6-12 months |
We are looking for a Research Study Technician to join our Insourcing Solutions team, located in South San Francisco, Ca. | 4/7/2023 |
| 4993 | Distributed Bio Mattawan, MI Research Analyst I - Pharmacy Bachelor's/Master's degree in a relevant field. Exp: 0 years |
We are seeking an experienced Research Analyst 1 for our Pharmacy Team in Mattawan MI. | 4/7/2023 |
| 4994 | Distributed Bio Newark, DE Research Associate I Bachelor’s degree (B.A./B.S.) or equivalent in a scientific discipline. Exp: 0-2 years |
We are seeking an experienced Research Associate for our Microbial Databases and Technology Transfer group located in Newark, DE. . This role will be Responsible for performing routine experiments and analyzing data to support new product and service development and associated support functions related to daily operations of Microbial Databases and Technology Transfer group. | 4/7/2023 |
| 4995 | Distributed Bio Reno, NV Research Analyst I - Bio/Immunology 1 Bachelor’s degree (B.A. / B.S.) in biological science or related discipline required. Exp: 6 Months |
We are seeking a Research Analyst Ifor our Safety Assessment site located in Reno, NV. This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 4/7/2023 |
| 4996 | Distributed Bio Bethesda, MD Bacteriology Technician - Floater ($1K Sign-on Bonus) Bachelor’s degree in Biological Sciences or related discipline is required. Exp: 0-2 years |
In the Bacteriology Technician Floater role, you will use existing SOPs and quality assurance standards to perform routine gross necropsy and parasitology exams of lab animals, as well as prepare and examine collected tissue for further evolution, and prepare blood samples for shipment. You will also be asked to gather and prepare lab materials; assist with receipt, stocking, and ordering of supplies; and assist with other duties in the main lab. In this role, you will also access, set up, and run incoming samples; as well as update appropriate databases and written logs for every sample; access and plate environmental submissions; and plate incubated broths onto appropriate media. The Bacteriology Technician Floater will also work interactively with various staff and customers to resolve concerns and offer technical assistance, including preparing and submitting written reports, charts, logs, and inventories. You will need to ensure accurate records of data, and you may be tasked with creating worksheets or spreadsheets to help the lab run more efficiently. You should expect to update records for instrument maintenance and performance, and you may be asked to make mechanical repairs, when possible. Other duties may include operating required equipment and general housekeeping, when required. | 4/7/2023 |
| 4997 | Diversigen Minneapolis, MN Laboratory Technician B.Sc. or M.S. degree in Biology, Biochemistry, Molecular Biology Exp: 0 - 1+ year |
As a Lab Technician I you will be expected to work collaboratively as part of a team. In this role, the Lab Technician I will be responsible for managing timelines, performing hands-on lab work, maintaining processing records and working in compliance with our accreditations and quality standards. | 4/7/2023 |
| 4998 | Bardy Diagnostics Round Lake, IL Research Associate II Master’s degree in chemistry such as analytical or organic chemistry. Exp: 0-2 years |
We currently have an opening for a Research Associate II who can effectively contribute to laboratory operations, laboratory analysts, and facilitate operational excellence in the Medication Delivery R&D Extractables and Leachables laboratories in Round Lake, Illinois. | 3/20/2023 |
| 4999 | Bardy Diagnostics Skaneateles Falls, NY Test Engineer Bachelor’s degree (Mechanical, Electrical, Software, Biomedical Engineering, or comparable technical discipline). Exp: 1 year |
As a member of the Baxter research & development team, you will assist in the world class development of new medical products.This role is responsible for Test Engineering as a member of the new product development team. In this position you will understand and define verification and reliability test protocols, contribute to customer needs, technical risks, product functionality and performance requirements. You will collaborate with other team members to determine what verification is required, including the amount of data required and the methodology for collecting and analyzing the data. Lastly, you will provide objective evidence that a product design meets its specified requirements and meets the identified user’s needs and intended uses. | 3/21/2023 |
| 5000 | Bardy Diagnostics Bellevue, WA Electrical Engineer (Hybrid) Bachelor's degree in electrical engineering or other technical or science field. Exp: 0 -1+ years |
Your talent is needed across a wide variety of industries. As an Electrical Engineer, you have a wide array of career choices, but are motivated by the opportunity to work in a company that supports innovation, professional development, and a purposeful mission. | 3/21/2023 |
| 5001 | Bardy Diagnostics Skaneateles Falls, NY Mechanical Engineer (Hybrid) Masters Degree in Mechanical Engineering, Mechanical Engineering Technology or equivalent. Exp: 1+ years |
A successful candidate in this role will engage in mechanical engineering activities as part of a broader team to develop new medical products. This role will ensure effective resolution to design related issues, develop new products to grow the business, and ensure compliance with product related standards. | 3/21/2023 |
| 5002 | Bardy Diagnostics Marion, NC Associate I, Quality Lab - Endotoxin B.S. degree in Microbiology, Biology, or related science Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 3/21/2023 |
| 5003 | Bardy Diagnostics Cleveland, MS Quality Associate I - Cleaning and Sanitization (3rd shift) Bachelor’s degree in the sciences or in engineering required. Exp: 1 year or more |
Responsible for quality assurance operation in the Solution Focus Factory (Plastic Pour Bottle/Glass/Vials Cleaning and Sanitization). Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Baxter quality practices. Provide incoming, in-process and finished goods testing support. Involved in the development and revision of new standard procedures and training of employees. Assist department managers in audits or assessments and closures. Analyze and complete customer complaints. Perform department equipment and process validations. Serve as technical liaison among QM functional groups as well as other departments in the plant. | 3/21/2023 |
| 5004 | BASi Research Products Raleigh, NC Formulation Scientist I B.S. degree in chemistry or related field. Exp: 1 - 3 years |
Responsibilities of the Formulations Scientist include (but are not limited to): prepare formulations for GLP-compliant and non-GLP studies; coordinate with Study Directors, Project Managers, and the formulation manager to ensure timely preparation and delivery of formulations for in-house studies; set up paperwork, perform calculations, and prepare formulations to support toxicology studies; coordinate and maintain ILS chemical repository inventory as needed; archive test chemical samples for studies, as needed; coordinate with Study Directors and outside analytical laboratories as needed for preparation and shipment of formulation samples; assist with company-wide collection and disposal of hazardous waste and equipment calibrations; perform laboratory maintenance tasks (e.g. equipment monitoring/maintenance, disposal of expired chemicals, laboratory clean-up, etc.); maintain supply inventories and prepare purchase orders as needed; maintain accurate study forms/records; handle data (e.g. organize data, prepare data tables); assist in the preparation of protocols, reports, SOPs, presentations as needed; work independently with detailed instruction and minor oversight; work in a team environment with a professional and positive attitude. Other duties as needed. | 3/21/2023 |
| 5005 | BASi Research Products Gaithersburg, MD Sample Management Technician I B.S., B.A., or A.A.S with strong emphasis in life sciences. Exp: 6 months |
Essential Position Responsibilities: Reviews study protocol and ensure study tasks and data for pre-clinical research studies are conducted in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. Independently generates study forms and worksheets. Prepares sample labels using automated and manual systems and labels cups and tubes for studies. Ensures adequate inventory/supplies are stocked for sample collection. Reviews sample labels and specimens to assure accuracy and quality standards. Prepares blood smears. Operates centrifuge for collected samples in accordance with SOP and protocol requirements and places resulting serum/plasma into appropriate storage tubes Assures proper storage conditions for sample types. Accessions specimens using automated and manual systems. Independently and accurately processes specimens within established metrics. Maintains equipment and instrumentation. Notifies Study Director of sample quality issues and documents appropriately. Manages multiple studies. Learns to perform protocol review in preparation for and attends PI meetings. | 3/21/2023 |
| 5006 | BASi Research Products Boulder, CO Lead Animal Technician B.S./B.A. in science (biology or equivalent). Exp: 1-year |
Assist Study Coordinators to ensure study protocol, schedules, formulations, and sample collections are correct and properly communicated to the research team. Assists Study Coordinators with the creation or verification of cage cards, sample collection prep labels, and data files. Assists in disease induction procedures. Administer doses of compounds to rats and mice via common dosing routes, including but not limited to oral, intravenous, subcutaneous, and intraperitoneal. Perform data collections, including weighing, clinical observations, health assessments, post operative monitoring, and disease progression scoring. Perform blood collections from rats and mice via tail vein, retro-orbital, and terminal blood draws. Processing whole blood collection via centrifugation for plasma and/or serum. Perform behavioral testing (Gait analysis, Von Frey, and Dynamic Weight Bearing testing, etc.) Assist in formulating experimental compounds for administration. Assist in rodent surgeries, including hemostasis, and suturing. Supports and participates in other duties and company initiatives as directed by management. Keep laboratory clean and stocked with supplies. Various software applications sustained by a Windows platform. (Excel, Word, PowerPoint, etc.) | 3/21/2023 |
| 5007 | BASi Research Products West Lafayette, IN Bio Analyst I B.S. in chemistry or biology. Exp: one year |
Conducts sample analysis with data interpretation and basic troubleshooting. Conducts method development and method validation experiments. Assists with general housekeeping and assist other departmental personnel as necessary. | 3/21/2023 |
| 5008 | Bausch & Lomb Greenville, SC Process Engineer I Bachelor’s degree in Chemical, Mechanical, Electrical or Manufacturing Engineering Exp: 1-2 years |
The Process Equipment Engineer will provide value added engineering and leadership to a variety of engineering projects for Lens Care Solutions manufacturing to increase performance, reduce cost, improve quality, and address critical obsolescence issues. Position will also support day-to-day uptime needs of process equipment across the manufacturing site. | 3/22/2023 |
| 5009 | Beckton Dickinson Salt Lake City, UT R&D Engineer I- MDR Remediation B.S. or MS degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or other related engineering field. Biomedical Engineering Exp: 1-2 years |
This position will lead the planning, testing, and documentation for EU (European Union) product launches. This position reviews the DHF for released products with regard to compliance to EU MDR, determine gaps, and develops mitigation plans and completes mitigation. The candidate will perform hands-on testing in optimization of a device; conduct process development activities to understand process inputs and outputs; assist/write technical documents, validation protocols and reports; prepare work instructions and standard operating procedures; assist in conducting design and process qualification and validation; support equipment development; support other activities from R&D, Quality, Operations, and Regulatory Affairs. | 3/22/2023 |
| 5010 | Be Biopharma Kendall Square, MA Contract - Sr. Research Associate, Bioassay Development BS or MS in Chemical Engineering, Biology, Analytical Chemistry, Biochemistry, Cell & Molecular Biology, or related discipline. Exp: 1-2 years |
This laboratory-based position is responsible for qualification, and execution of sample analysis using bioanalytical assays, primarily ELISA and MSD based assays, to support Be Bio’s R&D and research pipeline programs. This position will also have the scope of training on other assay types such as FACS and cell culture, to support other cross functional teams within the Be Bio organization. The successful candidate will utilize their knowledge of ELISA to apply these methods to execute assays, perform data analysis and present data to the internal teams. Prior experience in generating and maintaining test methods, assay worksheets, SOPs and R&D processes to GLP standards is desirable. This position has tremendous room for growth and opportunities across multiple areas of the R&D organization. | 3/22/2023 |
| 5011 | BGI San Jose, CA LC/MS Research Associate – Small Molecule B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
San Jose Mass Spec Lab of BGI Americas is seeking an exceptional and motivated research associate with competitive compensation. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up metabolomics and lipidomics capability in SJMS lab, 4) to support other departments when needed. A candidate with metabolomics/lipidomics LC-MS experience is a plus; a candidate with small molecule sample prep experience is a plus. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for metabolomic or lipidomics analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and working with biofluids is a plus. | 3/22/2023 |
| 5012 | BGI San Jose, CA LC/MS Research Associate – Proteomics B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
BGI Americas San Jose Mass Spec (SJMS) center is seeking an exceptional and motivated research associate to join our Proteomics department at our San Jose facility. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up additional proteomics capability in SJMS lab, 4) to support other departments when needed. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for proteomics and biologics characterization analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and, working with biofluids is a plus. | 3/22/2023 |
| 5013 | BigHat Biosciences San Mateo, CA Research Associate (Purification) BS or MS in biochemistry/chemistry/biology or related science field. Exp: 1-3 years |
BigHat Biosciences is looking for a motivated and energetic Research Associate with a strong background in protein purification to further advance BigHat’s platform for ML-driven antibody discovery and engineering. | 3/22/2023 |
| 5014 | BioFire Diagnostics Salt Lake City, UT Research Associate I or II B.S. in molecular biology, biology, biomedical sciences, or a related field is desired. Exp: One to two years |
The Molecular Systems Research Associate I or II (RA I/II) position is a full-time, non-exempt position. This position is part of a team working on various laboratory procedures involving nucleic acid isolation methods and PCR under general guidance. This person will work closely with other research associates or scientists in the research lab. | 3/23/2023 |
| 5015 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II Bachelor’s degree in a scientific discipline. Exp: RA I No experienceRA I No experience |
The Research Associate I is a technical hourly position with laboratory responsibilities. The RA I works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of FDA and other regulatory submissions. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The RA I position requires basic laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and BioFire. A Research Associate I may receive general or detailed instruction and supervision on routine work, and detailed instruction and supervision on new procedures and assignments | 3/23/2023 |
| 5016 | BioFire Diagnostics Salt Lake City, UT Software Engineer I/II/III - Data Engineer B.S. in a quantitative discipline: Computer Science, Software Engineering, Computer Engineering, Information Systems, Statistics, Mathematics, Engine Exp: 0+ years |
bioMérieux is a fast growing and profitable biotech company with a great opportunity for a Software Engineer that is interest in data engineering and software development. This engineer will be joining a team of Software Engineers to support the research and development at bioMérieux. | 3/23/2023 |
| 5017 | BioLegend San Diego, CA Research Associate - Antibody Development Bachelor of Science with a discipline in cell biology, immunology, and biochemistry preferred. Exp: 1-2 yrs |
This person would be responsible for developing phosphosite specific monoclonal antibodies in BioLegend derived from immunized animals by performing antigen preparation, host immunization, bleed analysis, and cell lysate preparation. Techniques involved in this job include antigen formulation, animal immunization and tissue harvesting, cell culture and antibody analysis using ELISA and Western blot techniques. | 3/23/2023 |
| 5018 | BioLegend San Diego, CA Biochemist I - Custom Solutions PURE Bachelor’s degree in Biochemistry, Chemistry, or other related area. Exp: 1 year |
BioLegend has an opening for a self-motivated individual with manufacturing experience in a fast moving and dynamic environment to join our Custom Solutions Team! The Biochemist I will be an integral member of a team, that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will manufacture custom purified antibodies under ISO13485 standards, troubleshoot problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 3/23/2023 |
| 5019 | BioLegend San Diego, CA Research Associate - Recombinant Protein & Molecular Cloning BS in biological sciences. Exp: 1-3 years |
This position is responsible for developing cutting edge recombinant protein research products in Molecular Cellular Biology group. The research associate will be involved on developing a new line of recombinant protein products by supporting other team members. The duties include preparing buffer solutions and cell culture media, performing PCR and DNA purification according to standard operating procedures, performing bacterial and mammalian cells cultures, and purifying recombinant proteins with affinity tag. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 3/23/2023 |
| 5020 | Bio-Rad Woodinville, WA Production Chemist I Bachelor’s degree in a life science or related field. Science knowledge to include Chemistry and Biology, Exp: 1-3 years |
Bio-Rad is looking for a Production Chemist to support our Woodinville Manufacturing Plant working in an FDA/ISO regulated manufacturing lab making reagents to support Bio-Rad’s product lines. In this role, you will be trained on following Material Batch Records for creating an array of buffers, diluents, conjugates, positive controls and negative controls. You will work with a small team to meet Bio-Rad’s production needs and assist in lab upkeep. | 3/23/2023 |
| 5021 | Bio-Rad Woodinville, WA Production Chemist I BS/BA Degree in the life science or related field. Exp: 1-3 years |
As a BioPlex Production Chemist, you will be part of a Team that supports Bio-Rad’s commitment to quality and safety. You will apply your science knowledge – and build on it - by formulating the various reagents for the BioPlex2200 Kits. This is accomplished according to FDA/ISO regulated manufacturing and per document methods employing Good Laboratory & Manufacturing Practices. This role is critical in maintaining the overall quality of Bio-Rad’s products and services. | 3/23/2023 |
| 5022 | Bio-Rad Woodinville, WA Quality Control Spec I BS/BA degree in the physical sciences. Exp: 1-3 years |
Bio-Rad is looking for a Quality Control Specialist to support Bio-Rad’s commitment to quality and safety by testing raw material and in-process commercial Quality Control testing. As a part of our Quality Control team, you’ll apply your science knowledge in testing BioPlex for assay component raw materials, bulks, fills and finished kits tested according to FDA/ISO regulated manufacturing employing Good Laboratory & Manufacturing Practices. This role is critical in maintaining the overall quality of Bio-Rad’s products and services. | 3/23/2023 |
| 5023 | Bio-Rad Irvine, CA Quality Control Spec I Bachelor's degree, or equivalent, in a life science or related field. Exp: 0-2 years |
Job requires Raw Material/Intermediate inspection & testing. Perform sampling and physical testing of raw materials as described in the documented procedures. Ensure documentation is accurate and revise as needed. Recognize and investigate out of specification results, out of trend results and report to supervisor. Assist with method correlation and other job-related tasks as required. Enter results into SAP & Laboratory Information Management System (LIMS) as required. Follow good laboratory practices & procedures. Work in a team environment & interface with other departments as required. | 3/23/2023 |
| 5024 | BioReference Laboratories Elmwood Park, NJ Medical Technologist (FT, 40 Hours) Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. One or more years of CLIA experience. Required for tech Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 3/23/2023 |
| 5025 | BioReference Laboratories Melbourne, FL Medical Laboratory Technologist (FT, 40 Hours) Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. One or more years of CLIA experience. Required for tech Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 3/23/2023 |
| 5026 | BioReliance Rockville, MD Associate Scientist 2 - 2nd Shift Bachelor’s Degree in a scientific discipline (e.g., Biology, Chemistry, Microbiology, etc. ) Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist 2 – 2nd Shift , you will perform assays and safety testing required to manufacture clinical and commercial products. You will make scientific observations, maintain detailed workbooks/documentation, and ensure all documentation fulfills generally accepted professional/industry standards. | 3/23/2023 |
| 5027 | BioReliance Temecula, CA Scientist I - Organoid Culture And Characterization Master’s Degree in Chemical Engineering, Biochemical Engineering, Cell Biology, Biochemistry, or other life science discipline. Exp: 1+ years |
Help identify, evaluate, and design new protocols for human organoid development Culture and Passage organoids under sterile conditions Characterize organoids using techniques like QPCR, RNA Seq, Confocal microscopy etc. Follow product development plan to create commercial products from PDOs and SCOs Develop key biological assays using PDOs and SCOs Train other lab members in new/ advanced techniques Lead technology transfer and training of manufacturing personnel Prepare technical data packets for commercial use Help develop relevant reagents for PDOs or other organoids Engage with internal/ external collaborators and customers as technical champion for PDOs Leverage specialized knowledge and analytical skills to solve complex problems Summarize and present experimental results in written and oral reports Present the company at international conferences/ webinars to promote our brand awarenes | 3/23/2023 |
| 5028 | BioReliance Indianapolis, IN QC Analyst I Bachelor’s Degree in Chemistry, Biochemistry, Organic Chemistry, or other scientific discipline. Exp: 1+ years’ |
The QC Analyst I is a technical entry-level position responsible for analytical testing of finished product, raw materials, stability and special test requests. This position also requires analytical testing in support of protocols related to method transfers, method validations, laboratory investigations, and instrument qualifications. | 3/23/2023 |
| 5029 | BioReliance Milwaukee, WI Scientist Production Associate - 2nd Shift Bachelor’s Degree in Chemistry or Chemical Engineering Exp: 1+ years |
An Associate Production Scientist will assemble, operate, clean, and disassemble complete flow chemistry equipment according to established procedures and following safety protocols. You will annotate completed steps and processes in batch records in accordance with good documentation practices. You will test in-process samples using GC, Karl-Fisher titration, HPLC, 1H NMR spectroscopy, and FTIR spectroscopy. You will lead innovation projects designed to improve processes and reduce costs. You will have a passion for producing quality products that meet our customers’ needs and expectations. This is a 2nd shift position, Monday - Friday 2pm - 10:30pm. | 3/23/2023 |
| 5030 | BioReliance St. Louis, MO CGMP Associate Production Scientist Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or other life science discipline Exp: 1+ year |
The Associate Production Scientist at MilliporeSigma is responsible for the manufacturing of active biopharmaceutical ingredients (APIs) Chemicals and bulk pharmaceuticals regulated by the Food and Drug Administration (FDA). The Associate Scientist is responsible for following manufacturing protocols, consistent with and established according to current Good Manufacturing Practices (cGMP) and ensuring the accuracy of documentation. 12-hour overnight shift (6pm-630am) Two-week rotation: Week 1 (Monday/Tuesday/Friday/Saturday) Week 2 (Sunday/Wednesday/Thursday) | 3/23/2023 |
| 5031 | BioReliance Indianapolis, IN Process Engineer Bachelor’s Degree in Chemical Engineering or Biochemical Engineering Exp: 1+ years’ |
As Process Engineer, you will be responsible for providing key engineering support and project coordination to all phases of plant operations. The Process Engineer is also responsible for interfacing with internal and external clients in support of product technology transfers and manufacture, as well as providing technical support for processes and product investigations. | 3/23/2023 |
| 5032 | Bio-techne San Jose, CA Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
Salary Range: $71,400 – 107,000 depending on experience and qualifications Are you awesome? Come join an awesome team, doing amazing science! Bio-Techne develops, manufactures, and sells innovative tools and high-quality reagent solutions for life science research, therapeutic manufacturing, and clinical diagnostics. Among the Bio-Techne brands is ProteinSimple, a company based in San Jose, CA, that manufactures innovative analytical instrumentation. ProteinSimple is home to the Applications Science Team, a team generating amazing new applications and content, leading impactful and often game-changing collaborations with key customers, key customer support, and fee-for-service custom method development. The Applications Science team is seeking a highly motivated Advanced Research Associate to join our ranks! In this position, you will work daily with innovative analytical platforms on cutting edge research areas alongside our scientists to contribute exciting data for scientific collateral and custom projects. | 3/23/2023 |
| 5033 | Bioventus Memphis, TN Quality Engineer I Bachelor’s degree in Engineering or Science discipline or equivalent technical field. Exp: Up to 2 years’ |
The Quality Engineer I provides Quality Engineering support to Manufacturing, Engineering, QC/QA, and Process Development and IT teams to ensure that products are manufactured with a high level of quality, while being in compliance with regulations governing medical device manufacturing. | 3/23/2023 |
| 5034 | BioVision Waltham, MA Senior Research Associate, Cell Engineering Master Degree in Life Science Exp: 0+ years |
We are seeking a Senior Research Associate to join our Waltham, MA team to provide cell culture support for both the high throughput workflow for KO cell line generation and the preparation and replenishment of these KO cell banks for internal and external customers. This is predominately a benchwork lab-based role and your daily activities will contribute directly to Abcam’s goals and values. | 3/24/2023 |
| 5035 | Blueprint Medicines Cambridge, MA Senior Research Associate, Biology BS in in cell/molecular biology, cancer biology, genetics or related field Exp: 1-3 years |
We are seeking a highly self-motivated research associate to join a team of scientists working towards the discovery of novel anti-cancer drugs for the treatment of targeted patient populations. | 3/24/2023 |
| 5036 | Cambrex Agawam, MA Clean Room Analyst - Microbiological Environmental Monitoring Bachelor’s degree or higher in Microbiology or related field. Exp: 12 months |
As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications using within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 3/24/2023 |
| 5037 | Cambrex Marlborough, MA Clean Room Analyst - Microbiological Environmental Monitoring Bachelor’s degree or higher in Microbiology or related field. Exp: 12 months |
As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications using within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 3/24/2023 |
| 5038 | Aimmune Therapeutics Leonia, NJ Laboratory Tech - 1st Shift Bachelor of Science degree preferred. Exp: 0 - 3 years |
Under the direction of the QC Laboratory Supervisor, the Lab Technician is responsible for performing routine laboratory support functions, cleaning of glassware and general housekeeping. Non-routine duties are performed in a learning capacity under direct supervision. Responsibilities are focused on less complex testing and support functions. | 3/14/2023 |
| 5039 | Aimmune Therapeutics Leonia, NJ Technical Services Scientist Bachelor’s Degree in Chemistry, Chemical Engineering, Pharmaceutical Science or other related discipline is preferred. Exp: 1-3 years' |
Under the direction of the Tech Services Manager, the CTAG Specialist - Solid Dose will work closely with multifunctional teams to help improve current products, address manufacturing issues, evaluate new technologies and/or ingredients, seek cost savings and maintain networks of external partners. Adherence to Standard Operating Procedures (SOP’s) and current Good Manufacturing Practices (cGMP’s) is required. | 3/14/2023 |
| 5040 | Aimmune Therapeutics Bohemia, NY Associate Chemist (Junior) Bachelor's degree in chemistry, biology, or a related science field Exp: 1 – 2 years |
The Associate Chemist applies knowledge and skills to perform diverse and complex laboratory procedures and /or specialized technical, administrative services requiring application of equivalent technical knowledge in a quality control laboratory. Also, responsible for adhering to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMPs) that are in effect assuring the quality and quantity of product produced. | 3/14/2023 |
| 5041 | Aimmune Therapeutics Bohemia, NY Associate Chemist (Junior) Bachelor's degree in chemistry, biology, or a related science field Exp: 1 – 2 years |
The Associate Chemist applies knowledge and skills to perform diverse and complex laboratory procedures and /or specialized technical, administrative services requiring application of equivalent technical knowledge in a quality control laboratory. Also, responsible for adhering to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMPs) that are in effect assuring the quality and quantity of product produced. | 3/14/2023 |
| 5042 | Akadeum Life Sciences Ann Arbor, MI Production Support Chemist Bachelor’s degree in the life sciences Exp: 1 - 3 years |
Akadeum is seeking a Production Support Chemist with an early-stage mindset who will help manufacture kits and materials to support customers and partnerships, following standard operations procedures under a quality system. In your role, you will also help with shipping and support R&D material requests as needed. The role may include other duties as required to support company growth and operations. You will bring outstanding communication skills, a very high level of attention to detail, and an enjoyment of processes. You enjoy following established procedures, along with taking pride in delivering high quality products to researchers. Being highly motivated to produce disruptive technology under timelines and comfortable working in a fast-paced setting both as part of a team and independently is also important. | 3/15/2023 |
| 5043 | Akoya Biosciences Marlborough, MA Quality Engineer Bachelor’s Degree in Engineering or technical discipline Exp: 1-3 years |
Akoya Biosciences is looking for a Quality Engineer to join our Quality team. Reporting to the Supplier Quality Engineering Manager, this individual will manage a variety of quality system functions of Akoya Biosciences’ growing Quality Management System (QMS), working with Quality Management, product development, manufacturing, supply chain, and other groups, to ensure compliance to ISO 13485 and medical device quality requirements. The individual must be able to work independently and resolve or escalate quality issues in a creative, collaborative, and timely manner. Core values must include commitment to customer and operations excellence with demonstrated ethics and integrity. The Quality Engineer will manage day-to-day QMS processes such as monitoring & measuring supplier performance, auditing, validation planning, change control, CAPA, complaint & nonconformance investigations, and design quality. The individual will also help to develop new processes as the QMS grows and will have opportunities to grow within the Quality group. | 3/15/2023 |
| 5044 | Akron Biotechnology Sarasota, FL Technician, Quality Control BS in Biology, Chemistry or related science discipline. Exp: 1 or more years |
Akron Biotech is continuing to transform and further its rapidly growing capabilities and is now seeking highly motivated professionals to join our expanding team. This is an exciting opportunity to play a critical role within our organization that is driving advanced therapy development and commercialization with high quality industrial scale solutions. We manufacture and distribute components and raw materials for cell therapy discovery, development, and commercialization to meet industry needs worldwide. We offer an array of highly competitive benefits and perks to our valued associates. | 3/15/2023 |
| 5045 | Allakos San Carlos, CA Research Associate/Senior Research Associate, Protein Biochemistry B.S. or M.S. in Biological Sciences or related discipline Exp: 1-3 years |
Allakos is a clinical stage company focused on developing therapeutic antibodies against inhibitory receptors expressed on key immune cells involved in allergic, inflammatory, and proliferative diseases. We are seeking a highly motivated Research Associate/Senior Research Associate with a strong background in protein biochemistry to join our R&D team. The selected candidate will be responsible for generating different types of proteins to support our lead and pre-clinical antibody programs. This position will provide the candidate an opportunity to perform a wide range of activities and expand/learn new techniques across the Protein Sciences Team. | 3/15/2023 |
| 5046 | AllCells Alameda, CA Laboratory Associate - CGT Bachelor’s degree in Life Sciences. Exp: 1 year |
The Laboratory Associate is responsible for processing and isolating human primary cells and conducting quality control analysis. | 3/15/2023 |
| 5047 | AllCells Woburn, MA Laboratory Technician- Woburn, Mass. Bachelor of Science degree with a focus in Biology, Chemistry, (or related field) Exp: 1+ years |
Discovery Life Sciences is a trusted provider of bioanalytic and biospecimen services to hundreds of customers across the U.S. and around the world. The Laboratory Technician/Scientist in this manufacturing environment, produces materials and enzymes that feed the manufacture of hepatocyte-related products. This Technician works with animal and human tissue and manufactures enzyme based products. This position will work on-site in Woburn, Massachusetts. | 3/15/2023 |
| 5048 | AllCells Newtown, PA Histology Technologist Master's degree in a laboratory science (i.e. biology, chemistry, or other lab science) Exp: We provide training |
Discovery Life Sciences is a specialty laboratory services provider at the forefront of using IHC as a biomarker platform for personalized medicine. With our expertise in IHC services focused on oncology, inflammatory diseases, as well as other disease states, we are developing novel cancer tests to improve cancer patient outcomes. The Histology Technologist contributes to our mission by supporting the Study Director throughout the duration of a project including sponsor and study director updates, developing study design, assisting with proposal writing, and presenting to clients. | 3/15/2023 |
| 5049 | AllCells Huntsville, AL Associate Scientist - Flow Cytometry BS in Biology, Chemistry, Biochemistry, Immunology, or related discipline. Exp: 1-2 years |
Discovery Life Sciences is a globally recognized contract services laboratory that leverages the most current technologies to comprehensively support discovery, translational, and clinical research for the Pharmaceutical, Biotechnology and Diagnostic industry as well as Academic and Research Institutes. The successful candidate will help build testing pipeline, support validation efforts, and execute clinical flow cytometry testing in clinical trials studies. This role will be important in the continued growth of Flow Cytometry within the company with an opportunity to work and grow in a fast-paced environment and make an impactful contribution to the growth of Discovery Life Sciences. | 3/15/2023 |
| 5050 | AllCells Huntsville, AL Histology Technician Bachelor's Degree Required Exp: one year |
Previous knowledge of Histology or Pathology and a scientific background is a plus. The Histology Technician will coordinate and support the work of our growing Pathology Team through our Whole Slide Imaging digital platform. These duties require the ability to communicate clearly with internal or external contacts, either verbally or in writing. The DLS FFPE laboratory is a fast-paced environment that requires a focus and a commitment to always do the job correctly because the work we do impacts research worldwide. Discovery’s quality samples offer our clients the greatest opportunity to develop new treatments and diagnostics for patients suffering from a variety of diseases. We work every day because these patients are waiting. | 3/15/2023 |
| 5051 | Alliance Pharma Malvern, PA Assistant Scientist II BA/BS or higher Exp: 1-2 years |
Performs routine lab work, sample analysis, and validation under limited supervision. | 3/16/2023 |
| 5052 | ALPCO Diagnostics Salem, NH Reagent Chemistry Associate Bachelor’s degree in the Sciences (preferably in Chemistry or Biology). Exp: 1 - 3 years |
The Reagent Chemistry Associate works under general supervision and is expected to follow established procedures in the manufacture of ELISA kits and components; can perform standard manufacturing procedures and has knowledge of commonly used laboratory concepts and practices; relies on instructions and established guidelines or protocols to perform job functions; self stater who can work under minimal supervision. | 3/16/2023 |
| 5053 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 3/16/2023 |
| 5054 | Norwich Pharmaceuticals Norwich, NY Quality Systems Specialist I Bachelor of Science in Chemistry, Life Science, Engineering Exp: 1 - 3 years |
The Quality Systems Specialist provides system administration and support of daily quality activities to ensure compliance with global regulatory requirements and guidelines (FDA, ICH, EU, WHO, etc.). | 3/16/2023 |
| 5055 | Amarex Clinical Research Ann Arbor, MI Technician II - Extractions Lab 2 year degree – Science Degree Exp: 1-5 years |
NSF International is currently has an opening for a Technician II – Extractions Lab to support the extractions staff. This lab is crucial in prepping samples from NSF's Prep Labs before sending the samples off to NSF's analytical laboratories. In this position, a candidate would use high attention to detail to perform extractions of water samples. | 3/16/2023 |
| 5056 | Amarex Clinical Research Ypsilanti, MI Engineering Lab Technician Bachelor or Associate degree in an Engineering or Scientific discipline Exp: One year |
As a Technician II for Engineering/Plastics, you will be responsible for conducting basic testing on plastics, pipes, fittings and other related plumbing products to specific standards and procedures. | 3/16/2023 |
| 5057 | AmbioPharm North Augusta, SC Microbiologist BS in Microbiology or life sciences. Exp: 1-5 years |
Perform procurement and testing of: city and pharmaceutical grade water per USP guidelines and SOP; product for bioburden, endotoxin per USP guidelines and SOP; stability samples per SOP; environmental monitoring sample (viable and non-viable) per USP guidelines and SOP, as scheduled (daily, weekly, monthly, quarterly) Support production in qualification of clean rooms and water systems. Data entry for trending reports Perform QC testing and release of microbiological media, reagents, and stock cultures Maintenance of stock cultures Use of aseptic technique for sampling and testing of all samples collected for microbiological analysis Documentation of all activities per current good documentation practices as described in SOP Use basic understanding of and knowledge of techniques, instrumentation and lab functions to identify problems, initiate investigations and support completion of work assignments Maintain inventory and ordering of supplies, media, reagents and stock cultures used in routine testing Support test method development and qualification/validation studies | 3/16/2023 |
| 5058 | AmbioPharm North Augusta, SC QC Chemist II Masters Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Hands on experience with HPLC, GC, IC, KF and other routine analytical equipment such as pH meter and balance. Perform quality control routine testing for raw material/ Intermediate/ Release / Stability testing Perform Method development and method validation execution, including writing protocols and reports. Must be proficient. Responsible for reviewing analytical laboratory raw data and electronic records. Participate in out of specification (OOS) investigations, as well as other deviations and writing investigation reports. Perform and review QC stability and release testing. Maintain the QC lab by ordering supplies routinely used for testing. Assist the QC/QA group with writing and editing of SOPs and STPs. Other duties as assigned. | 3/16/2023 |
| 5059 | AmbioPharm North Augusta, SC Purification Chemist I Bachelor of Science in Chemistry or equivalent Exp: 1-3 years |
Work in a cGMP environment to perform the peptide purification processes through chromatography as well as other various purification techniques. Use analytical skills to prevent and solve possible process complications and problems. Work as part of a team to complete specific projects in a timely manner. Follow approved cGMP manufacturing directions such as production batch records, standard operation procedures and standard test procedures. Help the team to install, test, operate and maintain equipment for manufacturing and in-process testing. Help the team to investigate any process deviation. Write deviation reports and initiate document change requests. Monitor compliance of maintenance and cleaning procedures of equipment and instruments used in GMP processes by periodically reviewing and signing off on maintenance and cleaning logs for each equipment. Help QC and QA departments to maintain the equipment calibration program. Must be willing to work rotating shifts and weekends. | 3/16/2023 |
| 5060 | AnaSpec Fremont, CA Synthesis Chemist I BS or above in Chemistry, Organic Chemistry, or related disciplines Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). As a member of the Synthesis department, the Synthesis Chemist I will work closely with the Purification, QC, and Sales & Business Development departments. | 3/16/2023 |
| 5061 | Anika Therapeutics Bedford, MA QA Compliance Specialist I Bachelor’s Degree or relevant experience in the life sciences. Exp: 1-2 years |
The Quality Assurance (QA) Compliance Specialist I performs compliance activities in support of production, engineering ensuring all activities are performed according to internal Quality System requirements, cGMP, FDA and ISO 13485 standards. Areas of responsibilities include receipt and review of documents such as charts, logs, batch records and approval of incoming materials for release. The position will provide floor support to production departments to include line clearances, in-process checks and assistance with investigations. The QA Compliance Specialist I performs quarterly audits support internal audits and participates in customer and regulatory audits as part of the Audit Team. | 3/16/2023 |
| 5062 | ANI Pharmaceuticals Baudette, MN QC Chemist/Sr. QC Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: QC Chemist – 1-3 years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 3/16/2023 |
| 5063 | Applied StemCell Milpitas, CA R&D Research Associate Master’s degree in Biochemistry, Cell Biology, or a closely related field. Exp: 18 months |
Support in vitro and in vivo gene editing applications, including molecular biology and cell work, for research and proprietary therapeutic technologies. Maintain the FACS (Flow Cytometry) equipment on a regular basis, perform daily quality control measurements, and initiate corrective actions in case of instrument failures. As directed, perform protein assay techniques, molecular cloning experiments, genotyping experiments, and ad nucleic acid isolation. Set up, operate, and maintain laboratory instruments and equipment, monitor experiments, collect data and samples, make observations, and calculate and record results. Analyze organic substances. Conduct research, and assist in the research, including the collection of information and samples, such as blood and animal tissues. Use computers, computer-interfaced equipment, robotics, and high-technology industrial applications to perform experiments and examinations. Monitor and observe experiments, recording production and test data for evaluation by research personnel. Analyze experimental data and interpret results to write reports and summaries of findings. Provide technical support and services for scientists and engineers working on employer’s proprietary genome editing and stem cell technologies. | 3/16/2023 |
| 5064 | Aquinnah Pharmaceuticals Cambridge, MA Research Associate Master’s degree in neuroscience, cell biology or related discipline Exp: 1+ years |
This position is laboratory-based and requires strong experimental skills with a background in cell biology, molecular biology, or biochemistry. Under supervision, the candidate will assist in duties including, but not limited to: cell culture maintenance, compound screening, biochemical assays, immunocytochemistry, and analysis using state of the art high-content imaging. Strong communication skills are required including the ability to analyze and report on the results. The candidate will be expected to function efficiently and cooperatively within a team and maintain accurate and clear project records. The ideal candidate will be creative, energetic and motivated. | 3/17/2023 |
| 5065 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. | 3/17/2023 |
| 5066 | Arvinas New Haven, CT Research Associate, Formulation R&D Bachelors of Science degree in a physical science. Exp: 1-2 years |
In the role as a Research Associate, you will prepare pharmaceutical formulations used in animal pharmacology and pharmacokinetic studies, and will work closely with compound management and in-life colleagues to make sure that dosing materials are available as needed. When issues related to formulation arise, you will serve as a primary problem-solving Formulation R&D contact for those in other disciplines. You will be responsible for ordering necessary excipients so that the animal studies will start on time and be comfortable dealing with last-minute scheduling changes. This position reports to the Research Scientist, Technical Operations and will be located at our headquarters in New Haven, CT. | 3/17/2023 |
| 5067 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree with an emphasis in science. Exp: entry-level |
The Molecular Biology Research and Development Department is seeking a research associate to work with department scientists and staff on the design, development, verification, and technical support of molecular in vitro diagnostic products for infectious diseases. The Research Associate I is a technical, hourly position with laboratory responsibilities. The RA I works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). The position requires basic proficiency in laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, data analysis, sequence analysis, and a dedication to the mission and goals of the department and bioMerieux. A Research Associate I will work collaboratively with other Research Associates, self-direct on routine work with no or minimal instruction and supervision, and will operate with general or detailed instruction and supervision on new procedures and assignments. | 3/17/2023 |
| 5068 | Astute Medical Salt Lake City, UT Research Associate I or II B.S. in molecular biology, biology, biomedical sciences, or a related field. Exp: One to two years |
The Molecular Systems Research Associate I or II (RA I/II) position is a full-time, non-exempt position. This position is part of a team working on various laboratory procedures involving nucleic acid isolation methods and PCR under general guidance. This person will work closely with other research associates or scientists in the research lab. | 3/17/2023 |
| 5069 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline or equivalent. Exp: 0-2 years |
This is a full-time non-exempt position. This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. This person works closely with other research associates in the department. Performs general lab duties, designs and conducts experiments, collects and analyzes data, and keeps an accurate record of all work done in accordance with the quality system. Requires some problem-solving skills. Normally receives general instructions on routine work and detailed instructions on new assignments. Reports to the Senior Research Associate or Scientist. | 3/17/2023 |
| 5070 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline or equivalent. Exp: No experience |
This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. Performs general lab duties, conducts experiments under the supervision of their manager, collects and analyzes data and keeps an accurate record of all work done in accordance with the quality system. Requires some problem solving skills. Normally receives general instructions on routine work, detailed instruction on new assignments. Reports to the Lab Supervisor or a Scientist. This is a full time non-exempt position. | 3/17/2023 |
| 5071 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline. Exp: 0-2 years |
The Research Associate I is a technical hourly position with laboratory responsibilities. The RA I works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of FDA and other regulatory submissions. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The RA I position requires basic laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and BioFire. A Research Associate I may receive general or detailed instruction and supervision on routine work, and detailed instruction and supervision on new procedures and assignments. | 3/17/2023 |
| 5072 | Atreca San Carlos, CA RESEARCH ASSOCIATE/SENIOR RESEARCH ASSOCIATE, HISTOLOGY BS or MS, preferably in biology or related field. Exp: 1-3 years |
In this position, the successful candidate will apply her/his basic science laboratory skills and expertise regarding histological tissue preparation and execution of tissue staining protocols (i.e.immunohistochemistry, immunofluorescence and simple stains) to contribute to Atreca’s antibody-target characterization research. The position reports to the Associate Director of Histopathology. The candidate’s expertise with immunohistochemistry, other histological methods will help us to discover and characterize novel tumor antigens and develop anti-tumor drugs. | 3/17/2023 |
| 5073 | Atreca San Carlos, CA TEMPORARY RESEARCH ASSOCIATE I, ANTIBODY INVENTORY Pursuing or completed Bachelor’s in Life Sciences or Engineering Exp: 1-3 years |
We are seeking an enthusiastic and motivated Research Associate to grow our Antibody Inventory efforts as part of the Protein Engineering group. The successful candidate will help manage and maintain Atreca’s antibody inventory and ensure suitability for downstream assays. This very central position will involve interacting with multiple research teams dedicated to the discovery of novel, antibody-based cancer therapies. | 3/17/2023 |
| 5074 | August Bioservices Nashville, TN Microbiologist I B.A./ B.S in Biology (or related) Exp: 0–2 years |
August Bioservices is looking for a Quality Control team member that is passionate and driven professionally. August Bioservices desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. Reporting to the Manager, Microbiology, the Microbiologist I will be responsible for performing biological assays of raw materials, in-process samples, finished product, and environmental monitoring samples. He/she will work with microbiology personnel to assure test results, procedures, and methods are written, maintained, executed, and approved in accordance with approved SOPs and regulatory requirements. | 3/17/2023 |
| 5075 | Avalign Technologies Fort Wayne, IN Quality Engineer BS in an engineering science. Exp: 0--3 years |
The Quality Engineer is responsible for supporting the organization to ensure quality and production goals are met. The Quality Engineer will utilize an engineering approach to improve manufacturing efficiencies and ensure quality standards of all products are met. | 3/17/2023 |
| 5076 | Avalign Technologies Greenwood, IN Quality Engineer BS in an engineering science. Exp: 0-3 years |
The Quality Engineer is responsible for supporting the organization to ensure quality and production goals are met. The Quality Engineer will utilize an engineering approach to improve manufacturing efficiencies and ensure quality standards of all products are met. | 3/17/2023 |
| 5077 | Avomeen Boulder, CO Research Technician BS Degree preferred but not required. Exp: 1-3 years |
Element is currently hiring for a Research Technician for our Boulder, CO location. The main responsibility of the Research Technician is to assist the Clinical Study Coordinator in facilitating the Study in each Laboratory in order to meet customer turn time and requests; to help ensure the Studies are performed to protocol(s) requirements; to ensure that the Studies meet requirements of the Quality System. The pay range for this role is between $25/hr.-$40/hr., depending on level of relevant experience. | 3/17/2023 |
| 5078 | Vapotherm Exeter, NH Quality Engineer I B.S. in Engineering or Science, or equivalent technical field. Exp: 0-2 years |
The Quality Engineer will be responsible for representing quality on projects and overall quality support to the organization including implementation of Vapotherm’s Quality Management System. While this role will be primarily focused on new product development, this role will support general sustaining activities as well as maintaining the effectiveness of the overall QMS. | 3/6/2023 |
| 5079 | VaxCyte San Carlos, CA Associate Scientist I, Protein Process Development & Manufacturing BS in Chemical Engineering, Biochemistry, or a related discipline Exp: 0-2 years |
Vaxcyte is looking for a motivated and collaborative individual to join the protein process development team. This is an entry level position, that can lead to a highly impactful career within Vaxcyte. By managing general lab work, generating needed materials for development use, and running assays that generate highly valuable data on process performance, this person can make a significant impact on the development of life-saving vaccines. As a member of the protein development team, this individual will have the opportunity to learn cutting edge technology using cell-free protein expression and Nobel Prize-winning click chemistry. | 3/6/2023 |
| 5080 | Vertical Pharmaceuticals Marietta, GA Analytical Chemist- Osmotica Bachelor's degree in Chemistry, Biochemistry, Biology or related field Exp: 0-2 years |
Description The Analytical Chemist I is responsible for testing of raw materials, in-process materials, and finished products to support release and stability programs. Essential Responsibilities: Perform laboratory tests such as sample extractions, set up and execution of chromatographic methods (HPLC and GC), and dissolution testing. Develops and executes UV, IR and PSD measurements and wet techniques as applied in the Pharmaceutical Analysis/Testing of products and excipients. Executes complex study designs. Executes components of method validation and method transfer projects. Assists with sample handling tasks. Documents laboratory work using laboratory notebooks in a detailed and accurate manner that meets cGMP requirements. Performs other duties as assigned or requested | 3/6/2023 |
| 5081 | VGXI The Woodlands, TX VALIDATION SPECIALIST Bachelor’s Degree or equivalent Exp: one to three years |
Support process and product quality programs including process, testing, and software validation, equipment calibration programs, and process monitoring activities by writing simple verification/validation documents, executing qualification tests, compiling data, drafting summary reports, and reviewing validation documentation to ensure products are manufactured in accordance with applicable regulatory guidelines, manufacturer’s specifications, client’s specifications, and VGXI’s requirements. Review, update and work with various departments to develop SOPs for existing and new equipment / tests / processes. | 3/6/2023 |
| 5082 | VGXI The Woodlands, TX QUALITY ASSURANCE SPECIALIST Bachelor's degree from four-year college or university Exp: 1-3 years |
This position will primarily be responsible for quality assurance and compliance activities related to ensuring that production, testing, and associated documentation meets applicable regulatory and client Requirements. | 3/6/2023 |
| 5083 | VGXI The Woodlands, TX DOWNSTREAM PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for downstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Downstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 3/6/2023 |
| 5084 | VGXI The Woodlands, TX UPSTREAM PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for upstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Upstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 3/6/2023 |
| 5085 | VGXI The Woodlands, TX MICROPROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for plasmid manufacturing operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Microprocess Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 3/6/2023 |
| 5086 | WaVe Life Sciences Lexington, MA Research Associate, Analytical Characterization/Development, Process Development, Oligonucleotide Chemistry B.S./MS in Analytical Chemistry/Organic Chemistry or related discipline Exp: 1-5 years |
Wave Life Sciences is seeking a highly motivated Analytical Chemist to join its oligonucleotide chemistry team in Lexington, Massachusetts. This is an ideal opportunity for an individual who is interested in cutting edge technologies and who thrives in a team-oriented, fast-paced, cross-disciplinary biotech environment. The candidate will take an active role in the analytical characterization of stereodefined oligonucleotides for discovery and development-related activities. | 3/7/2023 |
| 5087 | Frontage Chicago, IL QA Auditor, GLP BS/BA degree in basic or applied science (biology, chemistry, etc.) Exp: 1-2 years |
Position/Job Summary: The individual in this position supports studies of the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). The QA Auditor monitors study activities, facilities, equipment, personnel, procedures, and pertinent records to ensure that they satisfy appropriate domestic and international Good Laboratory Practice regulations, customer specifications and the company’s standard operating procedures. | 3/7/2023 |
| 5088 | Frontage Secaucus, NJ Lab Technician Associate or bachelor’s degree in a biomedical discipline or related scientific discipline Exp: 1 year |
Duties: Responsible for working under the guidance of the Lab Manager, Investigators; Management, Study Coordinator and Supervisor, to perform study procedures required in clinical studies conducted on behalf of sponsors at the Frontage Clinical Services. | 3/7/2023 |
| 5089 | Frontage Concord, OH Entry Level Lab Chemist B.S. in a chemistry or related field. Exp: entry level |
This position is for an entry level lab chemist. The ideal candidate will help support studies of preclinical drug development in a GLP environment. | 3/7/2023 |
| 5090 | Frontage Concord, OH Technician (Bioanalytical Scientist) B.S. in Biology, Biochemistry, Chemistry, Pharmacology, or related scientific discipline. Exp: 1-3 years |
Under general supervision, this position is responsible or conducting sample preparation for biological samples in an analytical chemistry laboratory and recording study results and observations. | 3/7/2023 |
| 5091 | Uptake Medical Johnson City, TN ERP Support Analyst - Johnson City, TN (On-Site) Bachelor’s degree in Systems Engineering, Computer Science, Information Technology, or Equivalent Exp: one years’ |
The ERP Support Analyst is the primary point of contact for technical support requests related to business-critical information systems serving as a liaison between functional and technical resources. This position is responsible for testing, troubleshooting, training, and documenting the complete order lifecycle including purchasing, EDI connections, order processing, manufacturing, and order fulfillment through warehouse distribution centers and related ERP tasks on an ongoing basis. Additional responsibilities include systems analysis, project tasks, workflow analysis, and technical communication and problem solving to ensure the systems’ performance meets company leadership and user satisfaction requirements. | 3/7/2023 |
| 5092 | Abbott Westford, MA Quality Engineer Master's degree Exp: 0-2 years |
Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents Our location in Westford, MA , currently has an opportunity for a Quality Engineer. | 3/7/2023 |
| 5093 | Abbott Columbus, OH Position Assistant Microbiologist-Microbiology-Columbus Plant- 3rd shift Science related Bachelor’s Degree Exp: 1-3 years |
Our Columbus, OH location is Abbott’s oldest nutrition manufacturing plant in the world. Working here, you’ll feel part of a family – a family of 400 that works together to help nourish the world. | 3/7/2023 |
| 5094 | Abbott San Diego, CA Production Chemist I BA or BS in Chemistry or Biological Sciences Exp: Zero to two years’ |
The position of Production Chemist I is within our Toxicology Business Unit located in San Diego, California. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. This job description will be reviewed periodically and is subject to change by management. | 3/7/2023 |
| 5095 | Abbott San Diego, CA Production Chemist I BA or BS in Chemistry or Biological Sciences Exp: Zero to two years’ |
The position of Production Chemist I is within our Toxicology Business Unit located in San Diego, California. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. This job description will be reviewed periodically and is subject to change by management. | 3/7/2023 |
| 5096 | Abbott San Diego, CA Production Chemist I BA or BS in Chemistry or Biological Sciences Exp: Zero to two years’ |
The position of Production Chemist I is within our Toxicology Business Unit located in San Diego, California. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. This job description will be reviewed periodically and is subject to change by management. | 3/7/2023 |
| 5097 | Abbott San Diego, CA Production Chemist I BA or BS in Chemistry or Biological Sciences Exp: Zero to two years’ |
The position of Production Chemist I is within our Toxicology Business Unit located in San Diego, California. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. This job description will be reviewed periodically and is subject to change by management. | 3/7/2023 |
| 5098 | AbbVie Lake County, IL Associate Scientist II - Physical Analytical Chemistry - Microscopy Master’s Degree or equivalent education Exp: no additional experience. |
Perform routine tasks competently and independently, and generate reliable and consistent results. Analyze and critique results, noting significant deviations. Troubleshoot experiments and instrumentation. Learn and understand new experimental techniques. Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences. Place data in proper scientific context by consulting and citing relevant literature. Demonstrate technical proficiency in his/her field. Impact projects predominantly through lab and/or pilot plant based activities. Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable. | 3/7/2023 |
| 5099 | AbbVie North Chicago, IL Associate Scientist II/ Scientist I, Protein Biochemistry MS in molecular biology, biochemistry, biotechnology, or other relevant biological sciences. Exp: 0+ years |
Seeking an experienced research scientist to join our Protein Sciences group at AbbVie's headquarters in the Chicago area. The successful candidate will work in a highly dynamic group to provide protein purification support for a variety of small molecule programs across different therapeutic areas in Discovery Research. The candidate should have protein purification experience and be proficient in all standard bioprocess and AKTA purifier. | 3/7/2023 |
| 5100 | AbbVie North Chicago, IL Associate Scientist II / Scientist I, Genome Biology - Genomics Research Center Associate II requires an MS in Cell, Molecular, or Developmental Biology, Biochemistry, Bioengineering, Immunology or a related life sciences field. Exp: Associate II: no experience |
The group is currently seeking a highly motivated Associate Scientist II / Scientist I to assist in the implementation of new ‘omic’ methodologies (epigenomics, transcriptomics, etc) to address gene function and role of causal variants (coding/ non-coding) supporting our Ophthalmology collaboration. | 3/7/2023 |
| 5101 | AbbVie North Chicago, IL Associate Scientist II / Scientist I, Cell Biology & Imaging Master’s Degree in Cell, Molecular, or Developmental Biology, or a related life sciences field. Exp: Associate II: MS and no experience |
We are seeking a talented and enthusiastic Associate Scientist II / Scientist I with experience in human cell culture and microscopy or high content imaging to support GRC’s growing collaboration with AbbVie’s Ophthalmology therapeutic area. This position will be primarily laboratory-focused and will support high content imaging assay and cellular model development, CRISPR-mediated phenotypic screening, and implementation of cutting-edge technologies to assess gene function and drug mechanism of action. Applicants should have broad laboratory research experience using cell and molecular biology techniques. Open communication and curiosity are essential. The candidate is expected to operate in a fast-paced, multi-disciplinary setting and must be able to execute multiple research projects in parallel.We are seeking a talented and enthusiastic Associate Scientist II / Scientist I with experience in human cell culture and microscopy or high content imaging to support GRC’s growing collaboration with AbbVie’s Ophthalmology therapeutic area. This position will be primarily laboratory-focused and will support high content imaging assay and cellular model development, CRISPR-mediated phenotypic screening, and implementation of cutting-edge technologies to assess gene function and drug mechanism of action. | 3/7/2023 |
| 5102 | AbbVie Worcester, MA Associate Scientist, Discovery Biologics BS or MS in Biology or related field Exp: BS: 0-5+ years; MS: 0-2+ years |
Biologics Discovery Sciences at AbbVie is seeking a highly motivated research scientist to join a dynamic team supporting biologics drug discovery. This position will impact projects through purification and characterization of biopharmaceutical products such as monoclonal antibodies in high throughput. The ideal candidate should have direct experience with mammalian tissue culture, protein purification, proficiency in standard chromatography techniques, protein characterization (e.g., MS, SEC), and binding assays (e.g., ELISA and flow cytometry). The applicant should be able to analyze, document, and report data. They should possess excellent communication skills and be comfortable presenting in group settings. | 3/7/2023 |
| 5103 | AbbVie Wyandotte, MI Associate Scientist, Chemistry I Bachelor’s Degree, or equivalent education. Exp: 0+ years |
Generate and analyze precise, reliable, and reproducible data in a timely manner, under the direction of a more senior scientific leader. Demonstrate experimental precision and should possess general understanding of core discipline. | 3/7/2023 |
| 5104 | Allergan Irvine, CA Associate Scientist II - In Vivo Master’s Degree or equivalent education Exp: no additional experience. |
Allergan Aesthetics Biological Research is seeking a highly motivated and innovative candidate who will contribute to multi-disciplinary research in a highly collaborative environment. The successful candidate will support projects aimed at pharmacological characterization of protein-based therapeutics. Under supervision by senior personnel, he/she will carry out a variety of in vivo pharmacological and behavioral assays to characterize and evaluate molecules of interest in rodent models. The candidate will participate in the design of research studies and independently generate precise, reliable, and reproducible data in a timely manner. He/she will demonstrate experimental precision, strong data analysis and interpretation skills, and excellent verbal and written communication ability. | 3/7/2023 |
| 5105 | Abeona Therapeutics Cleveland, OH Associate, Quality Control BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 0 to 4 years |
The Quality Control Associate performs routine laboratory activities in support of GMP testing for Quality Control. Testing includes raw material, packaging components, environmental monitoring, in-process and finished product. Interacts with employees internal and external to Quality Control. | 3/8/2023 |
| 5106 | Abveris Quincy, MA Research Associate: Protein Analytics Bachelor’s or Master’s degree in a scientific discipline required (Biology, Biochemistry, Biochemical Engineering) Exp: 1-3 years |
We are seeking a motivated individual to join our team and expand our bioanalytical department. Using state-of-the art technologies and workflows, this Research Associate would work with the Protein Analytics team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 3/8/2023 |
| 5107 | Acell Irvine, CA ENGINEER II, PRODUCT DEVELOPMENT M.S. in engineering or scientific discipline Exp: 0-2 years |
The Engineer II, Product Development will participate in projects of varying scope and complexity across Integra with a focus on neurological access and therapeutic devices. The Engineer II, Product Development will be responsible for the mechanical design and assembly of a project, assisting and leading cross-functional teams through some or all phases of the product development process under the guidance of senior engineering and leadership. | 3/8/2023 |
| 5108 | Adaptimmune Therapeutics Philadelphia, PA Manufacturing Cell Therapy Specialist (1st and 2nd shift) Bachelor degree in a cell biology, bioengineering or medical technology related field. Exp: 1+ years’ |
This role will provide support for the manufacturing of gene modified autologous T-cell product at our manufacturing site in the Philadelphia Navy Yard. The Specialist will perform cell processing activities, media formulation, product sampling, and other manufacturing needs as necessary, commensurate with the level of training and experience of employee. Work is primarily in Grade B and Grade C aseptic manufacturing environment, but may also include support of process development runs in the Manufacturing Science and Technology laboratory. | 3/8/2023 |
| 5109 | Adare Pharmaceuticals Vandalia, OH QC Chemist I Bachelor’s degree in Chemistry or closely related field Exp: 0-2 years' |
The QC Analyst is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 3/8/2023 |
| 5110 | Adicet Bio Redwood City, CA Manufacturing Associate II / III - Cell Therapy Bachelor’s degree in a biological science, engineering or related science discipline Exp: 1-3 years |
We are seeking a highly motivated and experienced individual with a strong background in cell process development/manufacturing. The Manufacturing Associate 2 will report to the Director of Manufacturing. In this role you will support the daily manufacturing operations of allogeneic CAR T cell therapies, assist with troubleshooting complex and non-routine equipment events, initiate and support deviations, and author SOPs. You will implement Good Manufacturing Practices and best practices to streamline manufacturing operations. You will demonstrate expertise and breadth of knowledge in executing processes across a variety of production activities such as cell processing, aseptic behavior, monitoring equipment and processes, product sampling, and conducting routine sanitization tasks to maintain facility and equipment. You will read and follow defined SOPs and policies, work independently on basic manufacturing tasks, identify, and communicate non-routine events, and review more complex decisions with your direct supervisor. | 3/8/2023 |
| 5111 | Adicet Bio Redwood City, CA Research Associate, RESEARCH: T CELL IMMUNOLOGY, CAR T CELL BS or MS/MSc in biological sciences or a related field. Exp: 1 to 3 years |
We are seeking a highly motivated candidate with a background in immunology to join the Adicet Research Team. The ideal candidate will have in-depth knowledge of T cell immunology and CAR-T cell development. The candidate will work as a part of a multidisciplinary team, utilizing the latest technologies for cell engineering and contributing to the generation of novel cell-based therapeutics for the treatment of cancer. | 3/9/2023 |
| 5112 | Adicet Bio Redwood City, CA Research Associate / Senior Research Associate, Upstream Viral Vector Group Master’s degree Exp: 1 year |
We are currently seeking a highly motivated Research Associate / Senior Research Associate with previous cell culture experience to assist in executing upstream operations for production of viral vectors. The successful candidate will join Upstream Viral Vector Team and contribute to the advancement of Adicet’s vector production platforms by set-up and maintenance of various cell cultures in adherent and suspension systems. The position also provides the opportunity to learn downstream processing procedures through interactions within the Viral Vector Development Team. The ideal candidate will work in collaboration with other Viral Vector scientists, as well as other cross-functional teams, to support the development of Upstream culture processes, help facilitate tech transfer to internal and external groups, and contribute to development of a best-in-class vector manufacturing process. This person will also work with other internal and external functional groups to help meet developmental timelines and continuity of manufacturing operations. This person would be a contributor to the Vector Team’s objectives in meeting project timelines, achievement of cooperate goals, and delivery of a consistent and robust viral vector product. | 3/9/2023 |
| 5113 | Adimab Lebanon, NH Research Associate - Sequencing B.S. in molecular biology, biochemistry, or a related field Exp: Entry Level |
We are seeking a skilled molecular biologist to join our team. This position will support Adimab's novel antibody discovery, maturation, and production platform by contributing to the sequencing core, performing core laboratory services, and taking on other responsibilities that may arise at a growing biotech company. | 3/9/2023 |
| 5114 | ADMA Biologics Boca Raton, FL Chemist I B.S. in Chemistry, Biochemistry, Molecular Biology or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Chemist I! The Chemist I will Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. | 3/9/2023 |
| 5115 | ADMA Biologics Boca Raton, FL QC Microbiologist I, Product Testing B.S. in Biological Science or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a QC Microbiologist, Product Testing. The QC Microbiologist, Product Testing will Perform quality control testing of raw materials, in-process samples and final products | 3/9/2023 |
| 5116 | ADMA Biologics Boca Raton, FL Raw Material Specialist I B.S. or associate degree in Chemistry, Biochemistry, Biology or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Raw Material Specialist I! The Raw Material Specialist I will perform quality control raw material processing and testing. Following general instructions on routine work and detailed instructions on new assignments. | 3/9/2023 |
| 5117 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences Exp: BS: 1-3 years; MS: 1 year |
Responsibilities: • Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing • Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. • Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. • Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. • Strict recordkeeping of all laboratory procedures. • Continue acquiring next generation sequencing knowledge to support molecular biology techniques. • Collaborate within the group and cross departmental to achieve goals. | 3/9/2023 |
| 5118 | Patheon St Louis, MO QC Scientist I (Bioassay) Bachelor’s Degree in a Biological Science or related field Exp: 1 year |
The QC Analytical Scientist’s primary responsibility is to perform routine to sophisticated QC testing pertaining ELISA testing and Cell Based Assays in accordance with cGMP regulations and Thermo Fisher standards to meet departmental and interpersonal goals. This position entails testing for GMP release and stability along with support for the validation and qualification of ELISA and Cell Based Assays. Additional responsibilities include supporting the department to establish robust work processes and assess for continuous improvement opportunities. The QC Analytical Scientist will report directly to the QC Analytical Bioassay Supervisor. | 2/28/2023 |
| 5119 | Patheon San Francisco, CA Cell Therapy Specialist Bachelor’s or Associates degree in a technical field desired. Exp: 1+ years |
Thermo Fisher Scientific is making a significant investment in the dynamic and rapidly growing Cell Therapy space. Our Cell Therapy organization within the Pharma Services Group, is one of the fastest growing areas of Thermo Fisher Scientific. We focus on providing development and clinical scale services for gene and non-gene modified cell processing for a variety of unmet medical needs. | 2/28/2023 |
| 5120 | Patheon San Francisco, CA Scientist I, Process Sciences BS or MS in biological science or engineering field preferred Exp: BS: 1+ years; MS: 0-1 years |
The Scientist I, with mentorship, will apply technical skills to conduct experiments and studies to support our clients cell therapy needs and to assist in meeting the goals of the Cell Therapy group. These functions may include but are not limited to activities such as cell isolation and separation, genetic modification (vector transduction and genomic editing), expansion methods (small, intermediate, and large scale), cryopreservation, technology transfer and design of technical documents. | 2/28/2023 |
| 5121 | Patheon Florence, SC Analytical R&D Scientist I Bachelor’s degree in chemistry or related field required. Exp: 1-2 years |
The Scientist I conducts laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Utilizes judgment in making adaptation and modifications on all assignments. Provides routine analyses in an analytical chemistry laboratory following standard practices. Performs analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results | 2/28/2023 |
| 5122 | Patheon Cranbury, NJ Research Scientist I Bachelor of Science (B.S.) in chemistry or related field Exp: 1+ years |
The Research Scientist I role is responsible for helping to develop recombinant cytokine products for the life-science research market. This role will report to our Director, Lab Operations. Day-shift Opportunity | 2/28/2023 |
| 5123 | Patheon Frederick, MD Scientist I, Formulation Bachelor’s degree in scientific field required. Exp: 1-3 years |
The Advanced Cell Systems Production team at Thermo Fisher Scientific is responsible for manufacturing various Primary tissue derived products including cells, RNA and subcellular fractions along with reagents and for a variety of biological applications. Our team is dynamic and fast paced, relying on teamwork, multitasking and communication within the team and the larger organization. We are seeking an energetic individual with strong communication, technical and operational skills to join our team. The candidate will follow SOPs and work in compliance with EH&S, GLP, and any other required manufacturing or company systems (e.g. E1, Agile, Trackwise, etc.). This position will be responsible for supporting the team in achieving daily production schedules and product quality goals. | 2/28/2023 |
| 5124 | PCI Pharma Services Bedford, NH QC Chemist I (Wed - Sat 6:30 AM - 5:00 PM) Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management | 2/28/2023 |
| 5125 | PCI Pharma Services Philadelphia, PA Process Engineer Bachelor's Degree in Mechanical or Packaging Engineering or related field Exp: 1-5 years |
The Process Engineer is responsible for identifying and mitigating packaging issues for existing business through strong engineering and process improvement methods. Provide technical leadership for new product launches. Lead continuous improvement activities. Secondary tasks include specify, purchase, and commission new equipment and manage capital finances. Provide technical support for new business (Sales/Business Development Support). All activities are focused around technical and operational support to the production, maintenance, and support staffs in the areas of process improvement, equipment modification and optimization, safety, and quality improvement, and increasing throughput. This is achieved through individual effort and facilitation of teams, tracking and analysis metrics, strong understanding and utilization of good engineering practices, project management, and the use of Lean Six Sigma techniques. Additionally, the Process Engineer will be responsible determining staffing, equipment needed, equipment purchase, equipment installation, component layout and line layout. | 2/28/2023 |
| 5126 | PCI Pharma Services Bedford, NH QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 2/28/2023 |
| 5127 | PCI Pharma Services Rockford, IL Laboratory QA Specialist 1 Bachelor's Degree in a related field Exp: 1-5 years |
The primary function of the Laboratory QA Specialist I is the timely and efficient review ensuring accuracy, completeness and compliance to in–house, customer and regulatory requirement, including data integrity, are met following the testing of pharmaceutical starting materials, components and finished products using techniques such as manual/automated titrations, UV, FTIR, LOD, Karl Fisher, Water activity and Pharmacopoeial testing i.e. LOD, RI, ID, Limit tests, Training of personnel in data review in area of expertise. Author OOS investigations, determination of root cause and develop and implementation of corrective and preventative actions. Author investigations into deviations from defined procedures. Review of regulatory bodies for changes applicable to the laboratory and ensuring that any changes are implemented. Maintain metrics with respect to area of responsibility. | 2/28/2023 |
| 5128 | PCI Pharma Services San Diego, CA Engineer, Sterile Fill & Finish Bachelor's Degree in a related field Exp: 1-3 years |
This role is responsible for engineering and technical oversight of the equipment and facilities of the Sterile Fill & Finish (SFF) implementation project(s) in San Diego. This person will become the technical Subject Matter Expert (SME) for the Cytiva isolator filling technology implemented in San Diego as well as the associated processing equipment related to formulation and sterile filling. This position will define relevant operational/technical standards and practices for the San Diego SFF operation and identify and drive the implementation of improvements to maximize throughput and capacity utilization. The role will interface with other PCI functions as well as external clients to implement new sterile filling projects and technologies into PCI GMP manufacturing. Responsible for the generation and execution of validation protocols, assistance in audits, determination of validation needs, and training of SFF staff. | 2/28/2023 |
| 5129 | Complete Genomics San Jose, CA Research Associate, Reagent Development Bachelor’s degree or Master's degree in Molecular and Cellular Biology, Chemistry, Biochemistry, or related field. Exp: 1-3 years |
This position is for a self-motivated and detail-oriented Research Associate with hands-on wet-lab experience to support our NGS service and lab. The candidate should be able to execute experiments independently, communicate with team players effectively, and interpret and document results in a timely fashion. | 2/28/2023 |
| 5130 | Poseida Therapeutics San Diego, CA Quality Control Analyst Bachelor’s or Master’s degree in life sciences or a related field Exp: 0-1 years |
Poseida is seeking an outstanding candidate to join our Quality team. The Quality Control Analyst is a member of a dynamic team that ensures the safety of our products at various points during the manufacturing process and confirms they meet predefined criteria. Working cross-functionally and collaborating with individuals and functions both within Poseida and at third parties, they will support the Quality department goals, participate in and promote Quality culture. | 2/28/2023 |
| 5131 | ProMed Molding Plymouth, MN Analytical Scientist Bachelor’s degree Exp: 0-3 years |
The Analytical Scientist performs a wide variety of analytical test method development, method validation, and routine testing activities for formulation and product releases. Including quality control related to testing of incoming materials, commercial, research and development pharmaceutical dosage forms and medical device combination products to support formulation and product release activities. The Analytical Scientist ensures ProMed’s brand, philosophy, systems, policies, and procedures are properly implemented and observed. | 2/28/2023 |
| 5132 | Prominex San Diego, CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
Prominex Inc. is a startup molecular diagnostic company with an experienced team of passionate and energetic scientists driven to create fast and affordable molecular diagnostic solutions across the globe. We are focused on infectious disease assays in point-of-care and home-based settings. We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 3/1/2023 |
| 5133 | Resilience Alachua, FL Specialist, Biomanufacturing B.S. (Biology, Microbiology, Chemistry or equivalent) Exp: 0-2 years |
This position will assist in production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). | 3/1/2023 |
| 5134 | Rocket Pharmaceuticals Cranbury, NJ Entry Level - Clinical Manufacturing Associate I - Upstream B.A./B.S. in Life Science, Biotechnology, ChemE, or similar relevant field Exp: 0 to 2 years’ |
As a Clinical Manufacturing Associate I, you will be part of a team responsible for the start-up of a cleanroom facility and the cGMP manufacture of viral vector therapies for use in clinical trials. Additional responsibilities include set-up, operation, and cleaning of equipment, equipment, and process monitoring and troubleshooting, receiving materials and supplies from the warehouse, maintaining supply inventories, creating technical documents, and maintaining cleanrooms and equipment in an inspection-ready state. The ideal candidate will also have a strong passion and curiosity for science and gene therapy with the desire to contribute individually and collectively in a dynamic, fast-paced environment. | 3/1/2023 |
| 5135 | Rocket Pharmaceuticals Cranbury, NJ Associate Scientist, Quality Control BS in Biology, molecular biology, virology, Life Sciences or equivalent Exp: 0 - 2 years |
We are seeking an Associate Scientist, Quality Control with the responsibility to support clinical manufacturing of a range of Gene Therapy products. Technical proficiency in analytical methodology for drug substances and drug products is required for gene-based products. | 3/2/2023 |
| 5136 | Tectonic Therapeutic Watertown, MA Research Associate/Senior Research Associate – Protein Sciences (Protein Biophysics) Bachelor’s or Master’s degree in analytical or biophysical chemistry or related discipline Exp: 1-3 Years |
The (Senior) Research Associate for Tectonic will be a highly collaborative team player who has experience characterizing proteins using a wide array of analytical and biophysical techniques. Hands-on experience with standard biophysical techniques is required and experience with assay development is a plus. The successful candidate will contribute to our core research capabilities and the development of our anti-GPCR antibody discovery platform. The candidate would conduct established biophysical assays and perform continuous development and improvement over time. This position represents a unique opportunity for the successful applicant to join an innovative start-up at the heart of the Boston biotech ecosystem and to contribute to its long-term Success. | 3/3/2023 |
| 5137 | Tevard Biosciences Cambridge, MA Research Associate, in vivo pharmacology BS/MS in Neuroscience, Physiology, Molecular/Cellular Biology, or a related Life Science discipline Exp: 0-2 years’ |
We are looking for Research Associate (RA-I or RA-II) with an innovative mindset, great attention to detail and ability to work collaboratively to solve problems, to help advance therapeutic candidates to the clinic. The successful candidate will have an opportunity to positively impact patients with serious unmet medical needs while working closely with our world-class scientific team, including with company’s scientific co-founders. In this position, you will collaborate with the in vivo pharmacology team to study effects of therapeutic lead candidates. The RA will work with animal models for rare genetic diseases and will be responsible for executing experiments to quantify molecular, cellular, and physiological readouts, in addition to supporting in vivo dosing studies and related research activities within the in vivo pharmacology group. This is an exciting opportunity for a motivated scientist to further develop their skills in neuroscience, physiology and gene therapy while helping to make an impact on lives of patients suffering from rare diseases. | 3/3/2023 |
| 5138 | Thrive Earlier Detection Cambridge, MA Research Associate I - Molecular Biology (Temporary) Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate I, with guidance from more experienced scientists, assists in the day to day experimental work that includes execution of bench experiments, and gathering and assembling of data. Working in a team setting, the Research Associate I will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 3/3/2023 |
| 5139 | Amniox Medical Miami, FL R&D Validation Engineer Bachelor of Science in Engineering (preferred), Biology, Chemistry, Biochemistry, or other technical discipline is required. Exp: 1 year |
The incumbent will be responsible performing basic to moderate level engineering tasks to support the development of new and existing HCT/Ps, medical devices, cosmetics, and biologics as well as to support compliance of the Research and Development laboratory to FDA and ISO standards. Primary responsibilities will include coordinating and supporting activities for product development; to include design verifications, process validations, and stability studies; as well as to support the validation/qualification of laboratory computer systems (including analysis spreadsheets, instrument software systems, laboratory information management system (LIMS), electronic laboratory notebook (ELN) systems, inventory management, and other specialized software). Additional responsibilities include supporting the manufacturing of developmental products in a Good Manufacturing Practice (GMP) facility and to support clinical and laboratory tasks and other duties for the Product Development department following Good Clinical Practice (GCP) and Good Laboratory Practice (GLP), where applicable. | 3/3/2023 |
| 5140 | Amniox Medical Miami, FL Associate I, Manufacturing P/T & F/T Bachelors or associates in biological sciences, or a related field preferred. Exp: 1-3 years |
The incumbent will be responsible processing human birth tissue in an FDA regulated environment and following all cGMP requirements. | 3/3/2023 |
| 5141 | Toxicon Somerset, NJ Research Analyst I - BioAnalytics Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1-3 years |
Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Research Analyst on our BioAnalytical team in Somerset, NJ. Are you interested in working in the research field? MUST have LCMS experience! The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time between 6am and 9am. Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Research Analyst on our BioAnalytical team in Somerset, NJ. Are you interested in working in the research field? MUST have LCMS experience! The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time between 6am and 9am. | 3/3/2023 |
| 5142 | Toxicon Bedford, MA Research Assistant · B.S. with a Biology background Exp: 1-3 years |
We are currently seeking a highly motivated, quality and detail oriented individual to join our In-Vitro Genetox team. The successful candidate will work closely with our study directors and quality assurance to ensure all study aspects are conducted per scientific and regulatory standards. This position is an integral component of a fast-paced environment. You will be joining a rapidly growing team and will be selected based on both experience/aptitude and a dynamic personality. The work is focused on in-vitro testing of medical devices and pharmaceutical products using Good Laboratory Practices (GLP). The main assays performed are AMES, MLA and Chromosomal Aberration testing. Studies are conducted under OECD and ISO guidelines, protocols, and Standard Operating Procedures.We are currently seeking a highly motivated, quality and detail oriented individual to join our In-Vitro Genetox team. The successful candidate will work closely with our study directors and quality assurance to ensure all study aspects are conducted per scientific and regulatory standards. This position is an integral component of a fast-paced environment. You will be joining a rapidly growing team and will be selected based on both experience/aptitude and a dynamic personality. The work is focused on in-vitro testing of medical devices and pharmaceutical products using Good Laboratory Practices (GLP). The main assays performed are AMES, MLA and Chromosomal Aberration testing. Studies are conducted under OECD and ISO guidelines, protocols, and Standard Operating Procedures. | 3/3/2023 |
| 5143 | Toxicon Somerset, NJ Veterinary Technician- Research Bachelor degree in Life Sciences, Associate degree in Laboratory Animal Technology or Veterinary Technology highly preferred. Exp: BS: No experience |
Explore research careers and be a part of something bigger as a Vet Technician-Animal Operations in Somerset, NJ. Do you have animal experience and a love for Science and Research? Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. Be a Part of the Bigger Picture of bringing medical advances to the forefront as quickly as possible!! Starting at $23.00 per hour with Career Growth potential as you master skills! $4,000.00 Sign On Bonus for New Hires! Explore research careers and be a part of something bigger! | 3/3/2023 |
| 5144 | Toxicon Somerset, NJ Habituation Study Technician Bachelor degree in Life Sciences Exp: BS: No experience |
Explore research careers and be a part of something bigger as a Study Technician-Animal Operations in Somerset, NJ. Do you have animal experience and a love for Science and Research? Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. Be a Part of the Bigger Picture of bringing medical advances to the forefront as quickly as possible!! Join the Somerset, New Jersey Team as a Habituation Study Technician! Implementation of animal habituation programs using positive reinforcement training and behavior scoring. | 3/3/2023 |
| 5145 | Toxicon Madison; Somerset; Greenfield, WI Study Technician- Anatomical Pathology Bachelor’s Degree in Life Sciences, or Associate Degree in Life Sciences, Histology, Laboratory Animal Technology or Veterinary Technology Exp: Graduating Seniors |
We have an exciting opportunity for December 2022 or May 2023 grads to join our Anatomical Pathology team in Madison, WI, Greenfield, IN or Somerset, NJ! Company Overview: At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions—because we know that knowledge has the potential to make life better for all. Here, you can apply your scientific curiosity in Biology, Animal Science, Zoology, Animal Behavior, Veterinary Technology, Dairy Science, Equine Science or similar majors to pursue advances in animal welfare and research the effectiveness, safety and toxicity of drugs in early development animal research studies. Your work will help medical, biotech, and pharmaceutical companies create life-saving vaccines and medicines that make a real impact on people’s lives. | 3/3/2023 |
| 5146 | Toxicon Bedford, MA Research Assistant - Chemistry Lab Operations Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1-3 years |
Explore research careers and be a part of something bigger as a Research Assistant for the Analytical Lab Operations in Bedford, MA! Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. As a Research Assistant I you will be responsible for providing technical expertise in supporting preclinical studies conducted under GLP, ISO 17025, and various other regulatory agencies. Research Assistants must work closely with study directors, analytical services staff, and quality assurance to ensure all study aspects are conducted in per scientific and regulatory requirements. Excellent communication skills needed as this position works closely with other research associates and scientists. Individual must be highly organized to handle multiple projects on an ongoing basis. | 3/3/2023 |
| 5147 | Trevigen San Marcos, CA Quality Control Specialist Bachelor’s degree in Biological Science, Chemistry, or related field. Exp: 1- 5 years’ |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. | 3/3/2023 |
| 5148 | Trevigen Minneapolis, MN Research Associate, Microbiology QC Bachelor’s degree in Microbiology or a related scientific field or equivalent Exp: up to 3 years |
The responsibilities of this position are to participate in the Microbiology QC testing and reporting procedures: set up, read, and report the microbial QC bioburden and sterility testing of various sample types using culture methods that include direct plating, broth inoculation, and membrane filtration. Performance of environmental monitoring for viable microbes, particle counts, and WFI/deionized water testing, reading, and reporting. Assist with efficacy and validation testing, new procedure development, new equipment IQ/OQ and calibrations. Perform general lab duties, assist with sanitization of clean rooms, and additional duties as assigned. | 3/3/2023 |
| 5149 | Trevigen Minneapolis, MN Advanced Research Associate, Analytical QC Master’s degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0 – 2 years |
The Advanced Research Associate, Analytical QC position will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, endotoxin assay, TOC, conductivity, pH, and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis, and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned. | 3/3/2023 |
| 5150 | Trevigen Minneapolis, MN Research Associate, QC Bioassay Bachelor’s degree in the biological sciences or equivalent Exp: 0 to 2 years |
Perform routine QC testing of antibodies and proteins using standard operating procedures (SOP) to determine the status of the product. Conduct stability testing on proteins and antibodies to predict shelf life. Perform a variety of tests including: Direct ELISA, Functional ELISA, Western Blot, Array, ELISpot experiments, and Impurity ELISA (mycoplasma, host cell protein, host cell DNA). Participate in investigations, internal requests, and custom projects. Actively take part in group projects as needed. Assist with improving lab protocols. Perform additional duties as assigned. | 3/3/2023 |
| 5151 | Triangle Insights Group Durham, NC Life Science Research Associate Bachelor’s degree in relevant field Exp: 0-3 years |
The Research Associate role is an entry-level position on a small team supporting the strategic recommendations Triangle Insights Group, a strategy consulting firm, provides to its diverse portfolio of clients in the life sciences industry. The focus of this position is to collect and analyze data from secondary sources, as needed by consulting teams, in the pursuit of answering the complex business problems facing clients. The perfect candidate has a strong track record of academic achievement and an interest in the life science and pharmaceutical industries. | 3/3/2023 |
| 5152 | Triclinic Labs Lafayette, IN Analytical Scientist BS in chemistry or related field. Exp: 1-3 years |
Job Description: Triclinic Labs is seeking a scientist to: • Carry out instrumental analyses. • Aid in maintenance and repair of analytical instruments. • Process analytical data for inclusion in reports. • Participate in instrument software validation as necessary. • Be involved in multiple projects concurrently and exhibit flexibility to meet changing priorities. • Provide high-quality work output and accurate record keeping • Comply with all regulatory and laboratory requirements and policies. | 3/3/2023 |
| 5153 | Universal Cells Seattle, WA Research Associate II, Clinical Gene Editing in Seattle, Washington An MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 3/3/2023 |
| 5154 | Universal Cells Seattle, WA Research Associate II, Molecular Analytics in Seattle, Washington MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the molecular engineering for our gene edited Universal Donor Cells with activities focused on performing custom TaqMan based PCR assays. They will work as a key member on a fast-paced team to run molecular assays to characterize our proprietary Universal Donor Cells. | 3/3/2023 |
| 5155 | Universal Cells Westborough, MA Research Associate II, Analytical Development in Westborough, Massachusetts MS Degree Exp: 0-2 years |
The Research Associate will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOPs, and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 3/3/2023 |
| 5156 | Universal Cells South San Francisco, CA Associate Engineer in South San Francisco, California BS in Chemical/Mechanical/Biological Engineering or Life Sciences; MS in Chemical/Mechanical/Biological Engineering or Life Sciences. Exp: BS: 1-3+ years; MS: 1-2+ years. |
As part of the Astellas Gene Therapy Center of Excellence (GTCOE) Engineering & Facilities enterprise team, the Associate Engineer will support day-to-day operations in our brand-new South San Francisco based Pilot Plant. The Pilot Plant affords a flexible, dynamic environment to execute small scale bioprocess operations for non-clinical material supply and to test innovative new processes and equipment to enable the next generation of manufacturing processes at Audentes. Responsibilities will include execution of test article production, engineering runs, and new process equipment evaluation. The role will include close collaboration with Process Development, Lab Management, Project Engineering, MSAT, and external vendors. This position is located in South San Francisco, CA. | 3/3/2023 |
| 5157 | Universal Cells South San Francisco, CA Pilot Plant Associate I in South San Francisco, California BS in Science or Engineering or equivalent experience Exp: Associate I: 1+ years |
Reporting to the Pilot Plant Manager, the Pilot Plant Associate will participate in upstream and downstream areas of AAV development in the Pilot Plant for new gene therapy programs and processes. This position will be located in South San Francisco, CA. | 3/3/2023 |
| 5158 | JGB BioPharma Consulting San Francisco Bay Area, CA Entry Level Organic Chemistry Contractor 2015 B.S. or M.S. in Organic Chemistry or Similar Exp: 1 year |
Join a mid-sized pharmaceutical company as they move their proven platform into a new therapeutic area Be involved in experimental design, applying findings to drive further research Organize results and present them in meetings with the broader team Continue to remain abreast on new developments in the field, apply this to your work in the lab Support overall laboratory efforts, including lab maintenance and supply preparation as needed. 2015 | 2/21/2023 |
| 5159 | Align Technology San Jose, CA Lab Technician Chemistry- Contractor Bachelor’s degree Exp: 0-2 years |
Align is looking for a Lab Technician Chemistry- Contractor for our San Jose California location. You will be responsible for supporting the new product development. The ideal candidate should have good understanding of working with chemicals and polymers. | 2/21/2023 |
| 5160 | Charles River Laboratories Cambridge, MA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking a Research Study Technician 1 for our Insourcing Solutions Department located in Cambridge, MA. Observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. | 2/21/2023 |
| 5161 | Charles River Laboratories Cambridge, MA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking a Research Study Technician 1 for our Insourcing Solutions Department located in Cambridge, MA. Observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. | 2/21/2023 |
| 5162 | Charles River Laboratories Cambridge, MA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking a Research Study Technician 1 for our Insourcing Solutions Department located in Cambridge, MA. Observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. | 2/21/2023 |
| 5163 | Charles River Laboratories Boston, MA Research Associate I Requires a BS in the biological sciences or relevant area Exp: 0-3 years |
Explora Biolabs a Charles River Company, is seeking a Research Associate to join its team in Boston, MA. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed in Essiential Duties and Responsibilities are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. | 2/21/2023 |
| 5164 | Charles River Laboratories S. San Francisco , CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking an experienced Research Study Technician I for our Insourcing Solutions site located in South San Francisco, CA. | 2/21/2023 |
| 5165 | Charles River Laboratories S. San Francisco , CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking an experienced Research Study Technician I for our Insourcing Solutions site located in South San Francisco, CA. | 2/21/2023 |
| 5166 | Charles River Laboratories Worcester, MA Research Technician I High school diploma or General Equivalent Degree (G.E.D.). Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: |
We have an exciting opportunity for a Research Technician 1 at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. We have an exciting opportunity for a Research Technician 1 at our Discovery site located in Worcester, MA. | 2/21/2023 |
| 5167 | Leica Biosystems Fargo, ND Process Validation Engineer I B.A. or B.S. in Biology, Biochemistry, Engineering or related science Exp: 0-3 years' |
The role of the Engineer I- Process Validation will be to support internal and external Cleaning Validation activities with projects focused on understanding and optimizing cleaning processes to improve product quality, cost, and process efficiency. Additional responsibilities include supporting Process Validation and Facility Environmental Monitoring Qualifications to ensure the production environment is compliant with regulatory requirements. This role has a large focus on documentation generation and some lab work both within the GMP manufacturing space and R&D environment. | 2/21/2023 |
| 5168 | Leica Biosystems Logan, UT Manufacturing Engineer Bachelor's Degree in a related engineering/technical degree Exp: 1 – 6 years |
Actively engage and support engineering priorities in response to manufacturing and plant priorities related to safety, quality, production, and cost/efficiency. Develop, lead or participate in various process improvement projects. Drive continuous improvement (LEAN) initiatives through application of sound engineering/reliability program elements and a data driven approach. Design, install, validate, and qualify new equipment to address key gaps in manufacturing Ensure that engineering support is performed in compliance with cGMP Regulations and Company Policies/Procedures. | 2/21/2023 |
| 5169 | Leica Biosystems Vancouver, British Columbia, CA Research Associate - Product Development Bachelors or Masters degree in a relevant scientific discipline (e.g. chemistry, biochemistry, pharmaceutical sciences, nanotechnology, materials scie Exp: 1 year |
Precision NanoSystems has an opening for a Research Associate, Product Development to join our growing team in Vancouver, BC. The successful RA will become an expert in the formulation and characterization of nucleic acid lipid nanoparticles (LNPs). They will design and perform experiments to support a variety of new product development projects, contributing to the development of novel technologies such as GenVoy-ILM delivery reagents for genetic medicine applications. The successful candidate will have a diverse set of laboratory skills and be technically excellent, with attention to detail and a track record of successful research contributions. | 2/22/2023 |
| 5170 | Leica Biosystems Ashland, VA Analytical Laboratory Technician-Coupons Associates or Bachelor’s Degree in Chemistry or related science degree Exp: 0-2 years’ |
The Analytical Lab Technician performs defined analytical procedures on various samples under the guidance of senior associates, provides basic support, inventory management and upkeep of equipment | 2/22/2023 |
| 5171 | IQVIA Indianapolis, IN Associate Scientist, Biotransformation Bachelor's Degree in chemistry, biochemistry, biology or related field required. Exp: 1 year |
Analyze and report in vitro and in vivo biotransformation studies, with focus on analytical method development, metabolite profiling, and reporting. Collaborate with senior staff regarding study execution as it relates to timelines, data quality, and interpretation of results. | 2/22/2023 |
| 5172 | MEDTOX South San Francisco, CA Lab Technician - Entry level, will train! BS/BA degree in Biology, Chemistry, or similar biological scientific discipline Exp: Entry-Level |
This is a great entry-level opportunity to join an innovative laboratory and receive targeted one-on-one training that will help the individual grow in a career in the biotechnology field! The schedule for this position will be Monday – Friday, 6am-2:30pm, with rotating weekends (one month on, one month off working weekends).This is a great entry-level opportunity to join an innovative laboratory and receive targeted one-on-one training that will help the individual grow in a career in the biotechnology field | 2/22/2023 |
| 5173 | PerkinElmer San Diego, CA Research Associate - Bioassay Bachelor’s Degree in Science (Biology, Immunology, or other related discipline) Exp: 0-2 years |
This position will contribute to the release of new GMP products by performing bioassay to test recombinant proteins and neutralizing antibodies. The main responsibilities include performing bioassay testing, troubleshooting bioassay, preparing documents following good documentation practice. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. The position requires careful documentation skills. | 2/22/2023 |
| 5174 | PerkinElmer San Diego, CA Biochemist I - Recombinant Purification Bachelor of Science in biological sciences Exp: 1 year or more |
This position is responsible for manufacturing cutting-edge recombinant protein research products in the Recombinant Manufacturing group. The biochemist will be involved in different stages of production of various recombinant protein products, with a focus on recombinant protein purification. Another part of the job responsibility includes preparing product/project-related documentation, and maintaining the record for recombinant protein products. | 2/22/2023 |
| 5175 | PerkinElmer Lafayette, CO Scientist 1 Bachelor’s Degree in Biology or similar life sciences degree Exp: 1-3 years |
Horizon has an exciting opportunity for an enthusiastic Scientist I for molecular biology/viral production. The Scientist I position will perform primary tasks in an ISO 9001:2015 biology manufacturing laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the processing and preparation RNAi and Gene Editing products including molecular biology bench work, cloning, viral production, nucleic acid purification, collection replication, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of molecular biology including cloning and mammalian tissue culture. | 2/22/2023 |
| 5176 | PerkinElmer San Diego, CA Research Associate - Antibody Development Bachelor of Science or equivalent degree with a course works in cell biology, immunology, and biochemistry Exp: 1+ years |
This position is responsible for producing monoclonal antibodies derived from various materials such as hybridoma cultures. Basic tissue culture and/or purification responsibilities include performing cell culture work, antibody purification and associated quality control steps including purity analysis, isotype testing, mycoplasma detection, Ig quantitation, and specificity measurement by assigned methods. Detailed performance documentation, database entry and report preparation are also required. In addition, efforts for technical troubleshooting, inventory and laboratory maintenance will be expected to support team. | 2/22/2023 |
| 5177 | PerkinElmer San Diego, CA Quality Control Associate I (PM Shift) Bachelor’s Degree in Science with previous experience in a laboratory setting Exp: 1+ year |
QC Flow Associates focused on cell & tissue culture are highly motivated team members that will primarily be responsible for the preparation of primary cells and the culture of various cell lines, as well as the set up of cell stimulations needed for flow cytometry testing of BioLegend products such as antibodies, protein reagents, buffers for immunology and related research fields. In addition, the employee may perform surface, intracellular, and multicolor testing and analysis. Primary responsibilities include performing experiments (e.g. cell culture, cell preparation and flow cytometry testing); production and analysis of reliable, reportable data; maintaining accurate documentation, utilization of internal company databases for product filing and retrieval; following company SOPs and ISO requirements. | 2/22/2023 |
| 5178 | PerkinElmer San Diego, CA Biochemist I - Custom Solutions PURE Bachelor’s degree in Biochemistry, Chemistry, or other related area Exp: 1 year |
BioLegend has an opening for a self-motivated individual with manufacturing experience in a fast moving and dynamic environment to join our Custom Solutions Team! The Biochemist I will be an integral member of a team, that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will manufacture custom purified antibodies under ISO13485 standards, troubleshoot problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 2/22/2023 |
| 5179 | Sanofi Framingham, MA QC Microbiology Analyst 1 (Wed-Sat 2nd shift) Bachelor’s Degree Exp: 0-2 Years |
This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs and relevant procedures for method development, qualification, validation, method transfer, product release, stability, and process validation and investigations. | 2/22/2023 |
| 5180 | Invitrogen South San Francisco, CA Associate Scientist - Organic Chemistry Bachelor's degree or master's degree in Chemistry, Process Chemistry, or Organic Chemistry. Preference to master’s degree. Exp: 1+ year |
As an Associate Scientist (Research Associate), you will use state-of-the-art technologies to perform high-quality research for key pharmaceutical clients across the industry. Your problem-solving skills are an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. You will join the Small Molecule team while working onsite at the client location to support various GMP/GLP campaigns. | 2/22/2023 |
| 5181 | Invitrogen Rockville, MD Associate Scientist - mRNA Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0-2 years |
To perform the following activities for Drug Product support. This list is not all-inclusive and is subject to the needs of the project, but they will be responsible for planning and executing experimental studies in the area of mRNA lipid nanoparticle production and process optimization. | 2/22/2023 |
| 5182 | Invitrogen Cranbury, NJ Research Scientist I Minimum Bachelor of Science (B.S.) in chemistry or related field Exp: 1+ years |
The Research Scientist I role is responsible for helping to develop recombinant cytokine products for the life-science research market. This role will report to our Director, Lab Operations. Day-shift Opportunity | 2/22/2023 |
| 5183 | Krystal Biotech Pittsburgh, PA Laboratory Specialist/Associate Bachelor’s degree (Information Technology, Life Sciences or Engineering) Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated Laboratory Specialist/Associate who will work under the direction of the Quality Systems Manager. This role will support the development of Laboratory & Quality Systems (LIMS, QMS, and DMS), as well as assisting lab personnel with troubleshooting and software issues. | 2/22/2023 |
| 5184 | Krystal Biotech Pittsburgh, PA QC Microbiologist (Cleanroom) Bachelor’s Degree (Biology or related Life Science) Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated Quality Control Microbiologist to drive and sustain a comprehensive Cleanroom Environmental Monitoring Program that ensures regulatory compliance and promotes a strong culture of environmental cleanliness. This role will support the growing EM Department in sample collection and laboratory analysis. | 2/23/2023 |
| 5185 | Krystal Biotech Pittsburgh, PA Research Associate, Analytical Sciences and Clinical Testing Services Minimum of a Bachelor’s degree (Biology, Biochemistry, Chemistry, or related science) Exp: 0-2+ years |
Krystal Biotech, Inc is seeking a highly motivated a Research Associate, Analytical Sciences and Clinical Testing Services to perform high quality analytical testing in support of Krystal’s process development and product development efforts. This position will be laboratory based. | 2/23/2023 |
| 5186 | LakePharma Lebanon, NJ Analytical Chemist I- (Quality Control) Bachelor’s degree in Chemistry or related field Exp: 0-1 years’ |
The Analytical Chemist I I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished formulations, stability samples and for special projects, method development/transfers and cleaning study qualifications. | 2/23/2023 |
| 5187 | LakePharma Rensselaer, NY Research Scientist I; Medicinal Chemistry Bachelors or Masters Degree with major in chemistry Exp: 0-5 years |
The Research Scientist I is an integral part of the Curia team, contributing to our success by the synthesis, purification and identification of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. | 2/23/2023 |
| 5188 | LakePharma Springfield, MO Quality Assurance Specialist I Bachelor’s degree in Life Science or related field Exp: 0-3 years’ |
Essential job duties • Maintain Quality databases including Archival and scanning of cGMP documents and records, Departures, media fill programs, and training files • Represent Curia Quality Assurance when managing issues that require immediate corrective action. Ensure such action taken is appropriate and correctly documented • Solicit feedback from various departments for operational improvement • Author, review, and/or approve Quality Management System documents, including, but not limited to, change controls, SOPs, deviations, CAPAs, etc. | 2/23/2023 |
| 5189 | LakePharma Hopkinton, MA Quality Control Lab Technician I AS required or BS preferred in life sciences including biology, immunology, biochemistry, process engineering or a similar biological science Exp: 0-3 years |
We are rapidly growing and seeking a talented individual to join our Quality Control Team as a QC Microbiology Technician. The role will report directly to the Supervisor of QC Microbiology and will be based in our Hopkinton, MA facility. The ideal candidate will support cGMP validation and routine release testing for raw materials, in-process, drug substance and finished product testing for products produced at the Hopkinton GMP manufacturing facility. | 2/23/2023 |
| 5190 | Larimar Therapeutics Bala Cynwyd, PA Associate Scientist/Scientist, Bioanalytical M.S. in Biology, Biochemistry, Chemistry, or related field Exp: 1 year’ |
Larimar Therapeutics is a clinical-stage biotechnology company focused on the treatment of mitochondrial related and other rare diseases. The company is recruiting a motivated Associate Scientist/Scientist, Bioanalytical. The incumbent will monitor bioanalytical activities at external partners in support of program development. This would be a good opportunity for people who would like to transit from bench work to project management. | 2/23/2023 |
| 5191 | Lygos Berkeley, CA Fermentation Process Engineer I-II B.S. in chemical engineering or related fields Exp: 1-2 years |
Lygos is seeking a process engineer candidate to maintain, set up, run, troubleshoot and clean pilot scale bioreactors. The successful candidates will have experience with instrumentation and hands-on experience working on pilot scale bioreactors. The candidate will report to the Director of Fermentation. | 2/23/2023 |
| 5192 | Lygos Berkeley, CA Fermentation Research Associate Bachelor’s degree in Chemical Engineering or a related field Exp: 0-3+ years |
Lygos is seeking a Fermentation Research Associate to maintain, set up, run and clean bench-top level bioreactors (0.25L-150L). The successful candidate will have experience with general lab procedures, sterile techniques, data interpreting/reporting and will be comfortable working in a fast paced, multitasking environment. This person will have ample opportunity to participate in other aspects of Lygos’ technical efforts, including media optimization, batch work in flasks and 96 well plates, downstream processing development, lab build-out and other aspects of technology development, deployment, and commercialization. The Lygos team works closely with all employees to support career development and facilitate the learning of new skills! | 2/23/2023 |
| 5193 | Mammoth Biosciences Brisbane, CA Research Associate II, CRISPR Platform (High-throughput Mammalian Screening) Bachelor’s degree in molecular and cell biology, immunology, biochemistry, or a related field Exp: 1+ year |
Mammoth is currently seeking a creative and detail-oriented Research Associate II with experience in molecular biology, next-generation sequencing, and/or mammalian cell culture to join our CRISPR Platform team. The successful candidate will work collaboratively with colleagues to develop and execute high-throughput experiments in mammalian cell lines to support the development of novel Cas nucleases for therapeutic genome editing. They will have the opportunity to contribute broadly across multiple technical areas, including automation, software tool development, synthetic biology, and high-throughput screening. This position requires adaptability, strong organizational and communication skills, and the ability to work both independently and collaboratively in a dynamic team-oriented environment. | 2/23/2023 |
| 5194 | Masy BioServices Wilmington, NC Associate Scientist I/II Bachelor’s degree in Chemistry or a related field. Exp: 0 – 4+ years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also assist with method development/method validation projects. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: CKF/KF, ICP-MS, Particle Size, CCIT, UV. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 2/23/2023 |
| 5195 | Masy BioServices Wilmington, NC Associate Scientist I/II Bachelor’s degree in Chemistry or related field Exp: 0 – 4+ years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. This position may also be required to work on method development/method validation projects. Typical types of testing include: assays (potencies, related substances, residual solvents, metals etc.), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, DSC, TGA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client/vendor supplied or developed by Alcami). The Associate Scientist II must have the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data is required. The Associate Scientist II will occasionally be called upon to support and mentor other Analytical Chemists within the lab. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 2/23/2023 |
| 5196 | Med Institute West Lafayette, IN Chemist I Bachelor degree in Chemistry or Chemistry related field Exp: 0-2 years |
The Chemist 1 positions will perform release testing on raw materials and finished products using United States Pharmacopoeia (“USP”) compendial methods, client methods, and methods developed in house. Assist in the development and validation of analytical methods for drug products, placebo, and raw materials in the Cook Biotech Analytical Laboratory. | 2/23/2023 |
| 5197 | Meridian Life Science Memphis, TN Senior Research Associate Masters’ degree from an accredited institution in a relevant scientific discipline such as Biology, Chemistry, Biochemistry, Molecular Biology etc. Exp: 1+ years |
The Senior Research Associate will be responsible for conducting research and providing technical assistance, within our Technical Operations and Development department, to drive the improvement and growth of our immunological reagent offerings including recombinant proteins, native antigens, antibodies, blockers, and custom manufacturing. The position is responsible for conducting research and performing upstream bioprocessing, downstream bioprocessing, and analytical analysis of biomolecules. The candidate will assist with the optimization and scale up of processes, troubleshooting manufacturing issues, improving product quality, and reducing manufacturing costs. The candidate will be responsible for performing routine laboratory maintenance and lab management duties including maintaining sufficient supply of reagents, cleaning and disinfecting of laboratory equipment, cleaning lab area, environmental monitoring, and filling out proper paperwork. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO13485 regulations. | 2/23/2023 |
| 5198 | Lonza Portsmouth, NH Quality Control Microbiology Analyst Nights BS, AA in Microbiology, Biochemistry or Related Science Exp: 0 yrs |
The QC Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. Also being able to participate in quality testing for ongoing customer stability studies. The QC Microbiology Analyst should be able to provide on-time, high quality results to meet Manufacturing demands. *This position is a night shift role that reports to work Mon-Fri 10PM-6AM*Training will be conducted during the day shift for a few weeks. While working 3rd shift, the employee will receive a 20% shift differential. While working on any Saturday or Sunday, this employee will receive an additional 5% shift differential. | 02/15/23 |
| 5199 | DiabetOmics Hillsboro, OR Research Assistant/Associate in Product Development (2 positions available immediately) BA/BS in a relevant biological science Exp: 1-2 years |
Diabetomics R&D group is currently seeking a Research Assistant/Associate to join our established team. Essential Functions: Supports the Diagnostic Product Development team. This is a hands-on, bench-level laboratory position. Tasks will include, but are not limited to: assay feasibility, assay development, optimization, reagent formulation, verification and validation studies. | 2/13/2023 |
| 5200 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 2/15/2023 |
| 5201 | Fluxergy Irvine, CA Process Engineer Engineering degree Exp: 0-2 Years |
As the process engineer at Fluxergy, you will be directly involved in the company’s production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process ownership while working with a small but passionate team. This position requires a deep, in-depth knowledge of manufacturing processes, stability and process control. | 2/16/2023 |
| 5202 | Fluxergy Irvine, CA Industrial Engineer Undergraduate or Masters degree in Industrial Engineering Exp: 1-2 years |
As the Industrial Engineer at Fluxergy, you will be directly involved in the company’s Production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process improvement, scale up and capacity planning while working with a small but passionate team. This position requires a deep, in-depth knowledge of lean manufacturing and six sigma methodologies. | 2/16/2023 |
| 5203 | Frontida BioPharm Vandalia, OH QC Analyst Bachelor’s degree in chemistry or related field Exp: 0 to 3 years’ |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 2/16/2023 |
| 5204 | Frontida BioPharm Vandalia, OH Raw Materials Chemist Bachelor or Master’s degree in Chemistry or related field Exp: Chemist I: 0-2 years’ |
The Raw Materials Chemist will report to the Manager of Raw Materials QC, and will perform chemical and physical testing on pharmaceutical raw materials (APIs, Excipients and Packaging components). | 2/16/2023 |
| 5205 | Frontier Medicines South San Francisco, CA Research Associate, Protein Sciences BS or MS in Biochemistry, Biological Sciences, or a related field Exp: 0-2 years |
We are seeking highly motivated research associates to join our group in South San Francisco, CA. This is an exciting opportunity for experienced and passionate associates or recent graduates to apply and expand their skills in protein sciences and contribute to the discovery of innovative therapies. The successful applicants will carry out experiments in protein expression, purification, and characterization to support biochemical assays and structure determination. Working closely with an experienced team of interdisciplinary scientists, the candidates will have regular opportunities to present findings to the Protein Sciences team. The ideal associates should have a strong desire to learn new techniques and incorporate new methodologies into their work, as well as be detail-oriented, self-motivated, well organized, and enjoy working and learning in a dynamic team environment. | 2/16/2023 |
| 5206 | Fujufilm Diosynth Research Triangle Park, NC Production Technician (Weigh & Dispense) BS/BA Exp: 1+ years |
Write and review standard operating procedures, buffer formulation records. Assist senior staff in implementing project safety and quality assurance programs in accordance with SOPs. Maintain the confidentiality of proprietary company information. Document and maintain activity records according to cGMP regulations and ensure junior team members are trained. Operate general production equipment such as Autoclaves, Analytical Scales, pH/conductivity meters, etc. Lead/Perform daily cleaning and sanitization of the weight and dispense area and manufacturing SAP transactions i.e. goods issue, goods receipt, goods transfer. Receipt & lot numbering of incoming materials. Issue of materials to process orders and cost centers. | 2/16/2023 |
| 5207 | Fujufilm Diosynth Thousand Oaks, CA Manufacturing Associate Bachelor of Science (B.Sc.) Exp: 0-3 years |
The Manufacturing Associate works as part of the manufacturing team to deliver high quality cell therapy materials during process transfers, routine production, and technology improvements. This position contributes to the successful delivery of released product in support of clinical trials and commercial production. | 2/16/2023 |
| 5208 | Fujufilm Diosynth Thousand Oaks, CA Associate Scientist, Process Sciences Master of Science (M.Sc.) Exp: 1+ years |
The Associate Scientist, Process Sciences, is a critical position responsible for development activities associated with cell therapy process development and design at Fujifilm Diosynth Biotechnologies, California (FDBC). This position provides hands-on support for all aspects of process development experimental design and execution, will be responsible for experimental process monitoring (data capturing), and process troubleshooting. This position will work closely with and/or under the direction of a Senior or Principal Process Development Scientist. | 2/16/2023 |
| 5209 | Fujufilm Diosynth College Station, TX Process Sciences - Engineer I Master’s Degree preferably in Chemistry, Biology, Life Sciences or related field Exp: 0-3 years |
The Engineer I functions within a team based organization to actively address complex cGMP manufacturing issues. The individual is responsible for analyzing process technologies in support of new project proposals and assist in the technical transfer into the manufacturing group. This individual must work in a collaborative manner coordinating the transfer of biological drug processes from process development (internal or client) groups in a CMO environment. | 2/16/2023 |
| 5210 | Fujufilm Diosynth College Station, TX Quality Control - Microbiology Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field Exp: 0-1+ year |
The Microbiology Analyst I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. | 2/16/2023 |
| 5211 | Generation Bio Cambridge, MA Associate / Senior Associate Scientist, Preclinical Research S. or M.S. Exp: 1 year |
Generation Bio is seeking an energetic and adaptable (Sr.) Associate Scientist to join our Preclinical Research Team, focusing on the liver platforms. This lab-based position will include both in-vitro and ex-vivo assay work, both routine and development. The ideal candidate will have a background with plate-based assays, assay development, mammalian cell culture and in-vitro studies. This role will be responsible for implementing cell-based and ex-vivo assays to characterize gene therapy candidates for a range of implications. | 2/16/2023 |
| 5212 | Gritstone Technology Cambridge, MA MOLECULAR TECHNOLOGY ASSOCIATE I/II Bachelor’s degree (or equivalent) in scientific discipline or a health-related field Exp: 0-2+ years |
The primary role of the Molecular Technology Associate I/II is to perform patient processing using established histology, and next-generation sequencing assays in the GMP Next Generation Sequencing (NGS) laboratory. This team is responsible for the GMP compliant processing of cancer patient samples through nucleic acid extraction and next generation sequencing. The ideal candidate will have patient-centric approach and experience in a regulated environment (CLIA/CAP, cGMP) and will be expected to maintain batch record reports, consumable inventory, equipment maintenance and calibration to maintain quality control and compliance. Individuals with experience as a Clinical Lab Technologist or Molecular Technologist are encouraged to apply. | 2/16/2023 |
| 5213 | Gritstone Technology Cambridge, MA RESEARCH ASSOCIATE I/II, NGS PROCESS DEVELOPMENT (Contractor) Bachelor’s degree (or equivalent) in scientific discipline or a health-related field Exp: 1+ years |
We are seeking a highly motivated, collaborative Research Associate I/II (Contractor) to support our NGS Process Development and Automation team in Cambridge, MA. The ideal candidate will have experience in a high throughput NGS laboratory setting and/or familiarity working in a regulated environment (CLIA/CAP, cGMP). Individuals with experience in cell culture, or as a Clinical Lab Technologist/Molecular Technologist are encouraged to apply. | 2/16/2023 |
| 5214 | Gritstone Technology Emeryville, CA RESEARCH ASSOCIATE I/II, VACCINE TECHNOLOGY Bachelor’s degree (or equivalent) in a scientific discipline or a health-related field Exp: RA I: 1+ year |
We are looking for an enthusiastic and flexible team player who will thrive in a fast-paced, dynamic, and highly collaborative environment. This individual will work in the molecular biology and vaccine technologies group and contribute to the development of novel viral and nucleic acid-based vaccines to meet unmet infectious disease and oncology needs. | 2/16/2023 |
| 5215 | Haemonetics Boston, MA Engineer, Disposables R&D Bachelor's Degree required in Engineering. Exp: 0-2 years |
Applies state of the art techniques in the area of expertise to sustain and/or develop new or improved products and processes. May lead small projects with moderately complex features under manager supervision. Plans, schedules and leads cross-functional team in detailed phases of the engineering work on a project. Must have experience or training and demonstrate proficiency in engineering disciplines (e.g. computer aided design, total quality management (6Sigma), statistical methods, materials science, design of experiments, design controls) and metrology. Must possess knowledge of related disciplines. | 2/16/2023 |
| 5216 | HemoSonics Raleigh-Durham-Chapel Hill, NC Manufacturing Technician Bachelor’s degree in Engineering technical field Exp: 1+ years |
The Manufacturing Technician will be responsible for building Instruments and the associated subassemblies by following the appropriate Work Instructions and Standard Operating Procedures within Instrument Manufacturing. This position will work with a team of Manufacturing Technicians and Engineers to provide input and support for device diagnostics and improvements as required. | 2/16/2023 |
| 5217 | HemoSonics Raleigh-Durham-Chapel Hill, NC Manufacturing Technician Bachelor’s degree in Engineering technical field Exp: 1+ years |
The Manufacturing Technician will be responsible for building Instruments and the associated subassemblies by following the appropriate Work Instructions and Standard Operating Procedures within Instrument Manufacturing. This position will work with a team of Manufacturing Technicians and Engineers to provide input and support for device diagnostics and improvements as required. | 2/17/2023 |
| 5218 | HighRes Biosolutions Beverly, MA Manufacturing Engineer I Bachelor's degree in engineering Exp: 0-3 years |
The Manufacturing Engineer I will develop and maintain methods, processes, and equipment necessary to achieve manufacturing and quality objectives. They will work with engineering to specify, build, test, and challenge new and existing product designs to improve efficiency, reliability, serviceability, manufacturability, and cost. The ideal candidate will be a self-starter who is comfortable working in a dynamic, team-based environment to reach common objectives with aggressive schedules. This role reports to our Manufacturing Engineering Manager. | 2/17/2023 |
| 5219 | HighRes Biosolutions Beverly, MA Associate System Design Engineer BS in Mechanical Engineering. Exp: 0-2 years |
As a Systems Design Engineer at HighRes Biosolutions, you will be heavily involved with all elements of our custom systems product life cycle. Youll work closely with the sales and applications team to turn a customers needs into an automated solution. Additionally, youll work closely with the operations team to turn your designs into fully functional systems. The systems you design will be used by top pharmaceutical and biotech companies around the world to help improve human health. The qualified candidate will have strong design capabilities with SolidWorks. A product development background for lab, medical or consumer products is beneficial. | 2/17/2023 |
| 5220 | HistoTox Labs Evansville, IN Histology Technician I Associate or bachelor’s degree in science related field Exp: 1+ years |
Perform diversified laboratory procedures and operations in the area assigned. | 2/17/2023 |
| 5221 | HistoTox Labs Westminister, CO Laboratory Animal Care Technician I College courses and or Associates or Bachelor’s degree in Animal Science or Husbandry are highly desirable. Exp: 0-3 years |
The ACT I is responsible for providing exceptional animal care to the research animals at Inotiv. This includes performing daily husbandry and care and of laboratory animals in a research environment as well as sanitization and preparation of animal housing equipment, including operation of a large bulk rack washer. The ACT I may be responsible for performing animal technical procedures and providing animal study support with supervision. The ACT I will work as part of a team conducting routine procedures required for vivarium operation. Individuals must demonstrate strong communication skills and be able to work efficiently in individual and team settings. | 2/17/2023 |
| 5222 | HistoTox Labs Rockville, MD Associate Scientist II BSc or MSc in Immunology, molecular biology, bioanalytical chemistry, drug metabolism, pharmacokinetics, or related science. Exp: 1-3 years |
The associate scientists should have knowledge and experience in ligand binding assay techniques, e.g., ELISA, MSD, Luminex, cell-based assays for PK and Immunogenicity determinations, or knowledge of PCR, DNA, RNA analysis, as well as flow cytometry. Due to the different techniques involved, some associate scientists would need essential experience in PCR, DNA, RNA, and flow cytometry analysis with a working knowledge of ligand binding assay techniques, e.g., ELISA (HELISA, etc.), MSD, Luminex, cell-based assays for PK and Immunogenicity determinations and LC-MS/MS. Depending on their experience and capabilities they will be placed in the different sections. | 2/17/2023 |
| 5223 | Ifyber Ithaca, NY Laboratory Technician BS degree Exp: 1 year (more preferred) |
The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. | 2/17/2023 |
| 5224 | Immuneering San Diego, CA Research Associate/Senior Research Associate M.S. in a scientific discipline. Exp: 1+ years |
We have two immediate openings for a full-time Research Associate/Senior Research Associate. The ideal candidate is quality and process-oriented, flexible and must enjoy the challenges of working in a fast-paced, biotechnology company with diverse people and drug programs. The Senior Research Associate is responsible for performing and collaboratively designing research and development experiments for projects and products within discovery/translational research teams. Regularly exercises technical discretion in the design, execution and interpretation of experiments that contribute to project goals. Contributes to project process within scientific discipline through innovative research. | 2/17/2023 |
| 5225 | Imperative Care Campbell, CA Quality Engineer II Bachelor’s degree in Engineering or related discipline Master’s degree. Exp: BS: 1+ years ; MS: 0+ years |
This position provides Quality Engineering support in the development, manufacture, and distribution of Imperative Care’s medical device products consistent with the Company’s Quality Policy and Quality Objectives. | 2/17/2023 |
| 5226 | Indigo Biosciences State College, PA Associate Scientist Master’s Degree in a relevant field of the biological sciences Exp: 0+ years |
The execution of experiments aimed at developing, optimizing, and validating new mammalian cell-based assays for INDIGO’s products and services portfolios. The large-scale manufacturing of mammalian reporter cells and assay kit components Performing routine quality QA testing of inventory stocks and executing inventory control policies to ensure the availability and integrity of INDIGO products. Assist Senior Scientists in the execution of contract service studies for INDIGO’s various biopharma, biotech, academic, and governmental clients. Execute ‘Inventory Control’ policies to ensure the availability and integrity of INDIGO Products. Routine Quality Assurance (QA) testing of Inventory stocks, and remanufacturing materials as needed to maintain appropriate levels of Inventory materials. Maintain and generate DNA stocks, as needed (plasmid purifications and gel analyses) Maintain an up-to-date, neat, orderly notebook according to the policies of the company. Contribute to weekly lab meetings. Associate Scientists are expected to present and interpret their own data for the Team, as well as to propose ‘next steps’ to advance their project. Further, Associate Scientists are expected to be fully intellectually engaged in critical evaluating other’s experimental data, as well as in the group processes of trouble-shoot technical problems, ‘brain storming’ the application of new or alternative technologies, and formulating and prioritizing sound experimental strategies to benefit individual & Team objectives. | 2/17/2023 |
| 5227 | IntelliSyn R&D Waltham, MA Research Associate BS or MS in Chemistry or related subject Exp: 6 months-2 years |
X-Chem is seeking a candidate for the position of Research Associate, Library Synthesis in its Discovery Chemistry group. X-Chem is a drug discovery company that uses DNA-encoded library (DEL) technology to discover leads for therapeutic targets. As a world leader in DEL technology, X-Chem collaborates with numerous pharmaceutical and biotechnology companies, resulting in over 70 licensed programs to date. | 2/17/2023 |
| 5228 | Pace Analytical Greenfield, IN Biologist Bachelor's degree in Biology Exp: 0+ years |
Candidate will use their skills and knowledge in Biology/Microbiology to support development of new products. | 2/17/2023 |
| 5229 | Pace Analytical Minneapolis, MN GC LC Chemist - Analytical Instrument Specialist BS degree in chemistry or related science Exp: 6 months - 2 years |
Working in our Technical Field Services (TFS) division allows chemists to perform hands-on work and interact directly with our clients. We specialize in servicing instrumentation such as GC, GC/MS, LC, LC/MS, IC, and Dissolution. While the instrumentation is complex, TFS has an extensive training program for new employees, as well as ongoing training to maintain the capabilities of our service staff. Our TFS Specialists have multifaceted skill sets including: strong technical aptitude, customer service, and problem resolution techniques. Additionally, we have been providing service to customers for eighteen years, achieving steady growth on an annual basis, which allows multiple advancement opportunities in MN, IL, IN, TX, and CA. Instrument Services Specialists are responsible for providing technical solutions and an advanced level of instrument support services to customers of TFS, including external clients, laboratory chemists within the Pace lab system, and departmental coworkers. They also provide our customers with a variety of support services associated with their analytical instrumentation. These services include routine maintenance, operational and performance testing, hardware and software troubleshooting, instrument repair, and personnel training.Working in our Technical Field Services (TFS) division allows chemists to perform hands-on work and interact directly with our clients. We specialize in servicing instrumentation such as GC, GC/MS, LC, LC/MS, IC, and Dissolution. While the instrumentation is complex, TFS has an extensive training program for new employees, as well as ongoing training to maintain the capabilities of our service staff. Our TFS Specialists have multifaceted skill sets including: strong technical aptitude, customer service, and problem resolution techniques. Additionally, we have been providing service to customers for eighteen years, achieving steady growth on an annual basis, which allows multiple advancement opportunities in MN, IL, IN, TX, and CA. | 2/17/2023 |
| 5230 | Pace Analytical Naperville, IL Scientist (Chemist, Lab Technician, Biologist) Bachelor's degree in Biology, Chemistry, Physics, and other related science. Exp: 6 months - 2 years |
Join us at Pace, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This is a lab based position. The candidate will be conducting various physical and chemical tests to assist scientists in making qualitative and quantitative analyses. Role may involve wet bench lab work, chemical handling, preparation of solutions/dilutions as well as routine analytical characterization and data analysis. Various shifts may be available. These positions are contracted positions which may last up to 12 months. | 2/17/2023 |
| 5231 | Pace Analytical Eagan, MN Scientist (Chemists, Lab Technicians) Bachelor's degree in Biology, Chemistry, Physics, and other related science. Exp: 6 months - 2 years |
Join us at Pace, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This is a lab based position. The candidate will be conducting various physical and chemical tests to assist scientists in making qualitative and quantitative analyses. Role may involve wet bench lab work, chemical handling, preparation of solutions/dilutions as well as routine analytical characterization and data analysis. Various shifts may be available. Several locations within the Minneapolis area and surrounding cities. These positions are contracted positions which may last up to 12 months. | 2/17/2023 |
| 5232 | Pace Analytical Chicago, IL Laboratory Technician Bachelors Degree in a science; Chemistry is preferred Exp: 1-2 years |
Join us as a Laboratory Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace® The laboratory technician will primarily help out a busy lab doing data entry. 70% of the role is expceted to be data entry. Note: This position is expected to last 6 months. | 2/17/2023 |
| 5233 | Invicro New Haven, CT Associate Scientist - Radiochemistry Bachelor’s level degree in analytical chemistry Exp: 0-3 years |
We are seeking a motivated and dynamic Analytical Chemist who can adapt to the fast speed and highly competitive environment. The candidate must have strong analytical chemistry experience to perform all the quality testing for radiopharmaceuticals produced at Invicro. Invicro does contract research focusing on the development of short half liferadiotracers for PET and SPECT imaging. The Analytical Chemist's primary purpose is to conduct the quality control testing of the radiotracers to ensure that all release criteria for human use are met. A strong background in HPLC and GC are required. Knowledge in aseptic techniques and cGMP is preferred. | 2/17/2023 |
| 5234 | Invicro Needham, MA Laboratory Assistant, Advanced Pathology Services Bachelor’s degree in a relevant biological science. Exp: 1-2 years’ |
Make an impact at a dynamic and growing company! Invicro seeks a Laboratory Assistant for Advanced Pathology Services to support for all routine Histology and IHC work pertaining to delivery of CAP/CLIA and GLP-like oriented lab services offered to external partners, including BioPharma, Academia, and Oncology Research Centers. Our laboratory performs high complexity immunohistochemistry and other advanced tissue analysis approaches unique to Invicro. This individual should enjoy challenging and analytical work and be motivated by the idea that together we can accomplish great things and make a positive contribution to society through our mission. | 2/17/2023 |
| 5235 | Vigene Biosciences Memphis, TN Manufacturing Associate - Cell Therapy 1 AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
We are seeking a Manufacturing Associate for our Cell Therapy Manufacturing Facility located in Memphis, TN. Work Schedule: Sunday-Wednesday Work Hours: 7:30 a.m-6:00 p.m. (CST) The Manufacturing Associate I is responsible for performing various manufacturing activities related to the start- up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 2/17/2023 |
| 5236 | Vigene Biosciences Memphis, TN Process Engineer I BS / MS / PhD in engineering or life sciences Exp: 1 year |
We are seeking a Process Engineer I for our Cell Therapy Manufacturing Facility located Memphis, TN. The Process Engineer I will provide equipment and facility technical support for incoming technology transfers of client manufacturing processes for advanced cell therapies. This role will participate in the transfer process and ensuring that the knowledge transfer to the manufacturing and supporting groups is efficient and effective. Additionally, this role will lead process equipment improvements, assessments, investigations, and implementations as governed by the site procedures and/or client requirements. | 2/17/2023 |
| 5237 | Vigene Biosciences Memphis, TN Quality Control Analyst I - Microbiology (EG) Bachelor's degree in Biology or relevant scientific discipline required. Exp: 0-2 years |
The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product-release testing, and raw material testing. The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success. | 2/17/2023 |
| 5238 | Vigene Biosciences Memphis, TN Biomanufacturing Technician-Shift A (Sunday-Wed/7:30 a.m.-6:00 p.m.) EG AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
We are seeking a Manufacturing Associate for our Cell Therapy Manufacturing Facility located in Memphis, TN. Work Schedule: Sunday-Wednesday Work Hours: 7:30 a.m-6:00 p.m. (CST) The Manufacturing Associate I is responsible for performing various manufacturing activities related to the start- up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 2/17/2023 |
| 5239 | Organogenesis Canton, MA Production Associate I/II- Apligraf (Sunday-Thursday) Associates or Bachelor’s degree in biology or related science Exp: 0 - 2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 2/7/2023 |
| 5240 | Organogenesis Canton, MA Quality Control Analyst I/II-Microbiology AS or BS degree in a Biology, Chemistry or equivalent QC related Exp: One (1) or more years |
The purpose of this position is the performance and reporting of microbiological testing for product release as well as environmental monitoring of all areas of the manufacturing facility, water sample collection and testing, compilation and entry of environmental monitoring data. The position ensures that the company goals for timely product testing are accomplished by being directly involved in the production of test results for product release and investigations. Other responsibilities or tasks as deemed necessary from time to time by the area’s supervisor. Some holiday work required. | 2/7/2023 |
| 5241 | Organogenesis Canton, MA Production Associate I/II- Apligraf (Sunday-Thursday) Associates or Bachelor’s degree in biology or related science Exp: 0 - 2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 2/7/2023 |
| 5242 | Meridian Medical Technologies Kalamazoo, MI Associate, Process Engineer Vaccine Injectable Manufacturing bachelor's degree Exp: 0-2+ years |
The Associate Process Engineer Vaccine Inj Manufacturing position will support projects and day to day operation of Sterile Vaccine Manufacturing Operations. This may include product transfer projects, cost improvement projects, capital equipment installations, Right First-Time initiatives, and safety and compliance driven initiatives for Drug Product Operations. | 2/7/2023 |
| 5243 | Meridian Medical Technologies Sanford, NC QA Associate - 2nd Shift Bachelor's degree n Biology, Chemistry, Engineering or related Technical Physical Science. Exp: 0-2 years |
You will be a member of Pfizer’s dedicated and highly effective Manufacturing Quality Assurance operations team. You will evaluate and review manufacturing activities in support of clinical and commercial batch production. Your expertise will help in identifying deviations from established standards, in the manufacturing of clinical and commercial batches. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. As a QA Associate, your focus on the job will contribute to achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. | 2/7/2023 |
| 5244 | Meridian Medical Technologies Pearl River, NY Associate Scientist, Immunology Master’s degree Exp: 1 year |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support the technology transfer and integration of new laboratory immunoassays into the cGLP space, support assay validation projects and monitor immunoassay lifecycle. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 2/7/2023 |
| 5245 | Meridian Medical Technologies Pearl River, NY Associate Scientist NGS BS Degree in Molecular biology, Virology, Immunology, or related scientific field Exp: 1-3 years |
We are seeking a highly motivated associate scientist with exceptional molecular biology knowledge to join Viral Vaccines department in Pearl River, NY. The ideal candidate will have some Next Generation Sequencing lab experience or have strong interests learning the technology and apply the technology to mRNA-based vaccine research and development. This role is wet laboratory based. The successful candidate will interface with a diverse set of colleagues to support the application of NGS technologies. You will be required to perform assigned lab experiments and record experiments details with E-notebook in a timely manner. You also be required to place and track reagents inventory, lab equipment operation and maintenance. In order to maintain compliance of regulated environment, you also will be responsible for the preparation and maintenance of associated documents and reports. Meticulous attention to detail, proficient reasoning and problem-solving skills and critical thinking are required. In addition to follow the established laboratory procedures, the individual should possess the curiosity and enthusiasm about the developmental work knowledge. The successful candidate should have solid background in DNA/RNA characteristics, qPCR assay development, genetics, and principles of genomic alterations. | 2/7/2023 |
| 5246 | Meridian Medical Technologies Pearl River, NY Associate Scientist, Molecular Testing Bachelor’s degree in a relevant field of science (E.g., immunology, bacteriology, or microbiology) Exp: 0 – 2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of generating high-quality molecular diagnostic data to support vaccine clinical development in a high‑throughput setting. The responsibilities include but are not limited to, performing manual and/or robotic molecular diagnostic testing, such as polymerase chain reaction (PCR). Other laboratory support activities include preparation of buffers and media, qualification of assay reagents, qualification and validation of assays, and other duties assigned as necessary. The incumbent will work in a team setting and will share roles and responsibilities as assigned by the Team Leader/Manager. Strong oral and written communication skills are essential. The position requires keeping current on documentation related to sample testing and assay development activities. As an integral member of this dynamic team, the incumbent must have a strong work ethic and be highly collaborative with other group members. The incumbent must be satisfied with repetitive and routine tasks, as this is a lab-based role. In addition, the incumbent must use good documentation practices, follow established safety policies and procedures, and perform all work in a compliant manner according to relevant SOP guidelines and GCLP and/or GMP guidelines, as required. | 2/7/2023 |
| 5247 | Meridian Medical Technologies Pearl River, NY Associate Scientist Bachelor’s degree in a relevant field of science (E.g., immunology, bacteriology, or microbiology) Exp: 0 – 2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of generating high-quality molecular diagnostic data to support vaccine clinical development in a high‑throughput setting. The responsibilities include but are not limited to, performing manual and/or robotic molecular diagnostic testing, such as polymerase chain reaction (PCR). Other laboratory support activities include preparation of buffers and media, qualification of assay reagents, qualification and validation of assays, and other duties assigned as necessary. The incumbent will work in a team setting and will share roles and responsibilities as assigned by the Team Leader/Manager. Strong oral and written communication skills are essential. The position requires keeping current on documentation related to sample testing and assay development activities. As an integral member of this dynamic team, the incumbent must have a strong work ethic and be highly collaborative with other group members. The incumbent must be satisfied with repetitive and routine tasks, as this is a lab-based role. In addition, the incumbent must use good documentation practices, follow established safety policies and procedures, and perform all work in a compliant manner according to relevant SOP guidelines and GCLP and/or GMP guidelines, as required. | 2/7/2023 |
| 5248 | Meridian Medical Technologies Pearl River, NY Associate Scientist Molecular Testing Bachelor’s degree in a relevant field of science (E.g., immunology, bacteriology, or microbiology) Exp: 0 – 2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of generating high-quality molecular diagnostic data to support vaccine clinical development in a high‑throughput setting. The responsibilities include but are not limited to, performing manual and/or robotic molecular diagnostic testing, such as polymerase chain reaction (PCR). Other laboratory support activities include preparation of buffers and media, qualification of assay reagents, qualification and validation of assays, and other duties assigned as necessary. The incumbent will work in a team setting and will share roles and responsibilities as assigned by the Team Leader/Manager. Strong oral and written communication skills are essential. The position requires keeping current on documentation related to sample testing and assay development activities. As an integral member of this dynamic team, the incumbent must have a strong work ethic and be highly collaborative with other group members. The incumbent must be satisfied with repetitive and routine tasks, as this is a lab-based role. In addition, the incumbent must use good documentation practices, follow established safety policies and procedures, and perform all work in a compliant manner according to relevant SOP guidelines and GCLP and/or GMP guidelines, as required. | 2/7/2023 |
| 5249 | Regeneron Tarrytown, NY Temp - Research Pharmacokinetics BS degree in biology or a related field Exp: 1-3 years |
Regeneron's Research Pharmacokinetics team within our Therapeutic Proteins organization is looking for an energetic Temporary Associate to join the team. In this exciting role, you will be expected to provide sample analysis assistance of timeline driven experiments. | 2/9/2023 |
| 5250 | Regeneron Tarrytown, NY Associate Scientist, Protein Expression Sciences BS or MS in a scientific field Exp: 0-3 years |
We are seeking a Associate Scientist to join the Protein Expression Sciences team. In this role, you will be responsible for generating manufacturing grade clinical cell lines for production of therapeutic antibodies to support the Regeneron pipeline. | 2/9/2023 |
| 5251 | Regeneron Tarrytown, NY Associate Scientist, Immunology MS Exp: 1+ years’ |
VelocImmune (VI) Next is a technology development group at Regeneron that invents and develops state-of-the-art tools for biologic drug discovery. We are seeking a motivated, highly organized scientist to support our investigations of new antibody and cell-based therapies. This is an opportunity for a researcher with strong molecular & immunology skills to contribute to the development of industry-leading technologies and medicines. | 2/9/2023 |
| 5252 | Regeneron Tarrytown, NY Associate Scientist, Immunology (In-Vivo) BS/MS Exp: 1-3 years |
We are seeking a motivated Associate Scientist to join a highly interactive immunology team. You will work on a team that develops and performs in vivo models for different asthma/allergy/autoimmunity diseases. This work will support to screen antibody candidates in mouse models, provide cytokine profiles after antibody treatment. | 2/9/2023 |
| 5253 | Regeneron Tarrytown, NY Associate Scientist, Clinical Bioanalysis BS degree or MS degree in a scientific field Exp: 0-3+ years |
Regeneron's Clinical Bioanalysis group, located in Tarrytown NY, is seeking a Associate Scientist. | 2/9/2023 |
| 5254 | Regeneron Tarrytown, NY Associate Scientist (Cell Culture for Therapeutic Antibody Discovery) BS degree or MS degree in a scientific field Exp: 0-3+ years |
Regeneron's Protein Expression Sciences (PES) group, located in Tarrytown, NY, is seeking a motivated Associate Scientist to join our human antibody isolation team, which contributed to the development of Regeneron’s Sars-Cov2 antibody cocktail (REGEN-COV). You will play an integral part in the identification of antibodies to treat diseases with unmet medical needs. The primary functions of this position are the isolation of monoclonal antibodies from human donors against diverse disease targets (eg. infections, immune disorders, etc) and the development of new antibody isolation technologies. Some experiments will require mice work such as organ harvesting and dissection. | 2/9/2023 |
| 5255 | Steris St Louis, MO Associate Scientist I- Microbiology Bachelor degree in Biology, Microbiology, Molecular Biology is preferred. Exp: 0-5 years |
Position Description Under close direction of supervising scientist or manager, completes assigned laboratory studies/tasks which include: - Accurate and thorough recording of raw data. - Mathematical analysis and data compilation. - Discussion of results. | 2/9/2023 |
| 5256 | West Pharma Exton, PA Associate Scientist, 2nd Shift, Lab BS in Chemistry or related technical degree Exp: 0 - 3 Years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment, while integrating into a diverse technical team. | 2/9/2023 |
| 5257 | West Pharma Exton, PA Associate Scientist, Raw Materials Lab BS in Chemistry or related technical degree. Exp: 0-3 years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment. | 2/9/2023 |
| 5258 | West Pharma Exton, PA Associate Scientist Lab Release BS in Chemistry or related technical degree. Exp: 0-3 years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment. | 2/9/2023 |
| 5259 | West Pharma Kinston, NC Lab Associate, Kinston Bachelor’s degree in Microbiology or Science related discipline. Exp: 1-3 years |
In this role you will perform all required routine testing (Bioburden Silicone, Particle, Endotoxin) to support product release, including water testing, environmental monitoring. Support other laboratory functions as needed | 2/9/2023 |
| 5260 | West Pharma Exton, PA Associate Scientist Lab Release BS in Chemistry or related technical degree. Exp: 0-3 years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment. | 2/9/2023 |
| 5261 | Acrotech Biopharma East Windsor, NJ MICROBIOLOGIST Master of Science Exp: Up to 3 years |
Microbiologist will perform a variety of Microbiology testing to assess the strength, identity and purity of test samples and/or materials. The Microbiologist will work as a member of team to effectively plan and Microbiology testing using established (official in USP and/or in-house) test procedures. The Microbiology may execute 90% - 100% of their work at the bench level. | 2/9/2023 |
| 5262 | Cell Signaling Technology Beverly, MA Senior Research Associate Masters degree in Biological Sciences or related degree Exp: 1-2 years |
The Multiplex Assays Development team is growing, and we are looking for a highly motivated Senior Research Associate who is passionate about collaborating with a team of scientists to develop and commercialize complex novel technologies for visualizing biology. A successful candidate will have the opportunity to independently prepare and maintain an inventory of reagents and buffers in order to perform multiplex immunofluorescence experiments, analyze data, and communicate results to the team. This cross-functional, team-oriented position requires strong organizational skills, exceptional attention to detail, and robust scientific communication skills. | 2/9/2023 |
| 5263 | Cell Signaling Technology Beverly, MA Senior Research Associate Masters degree in Biological Sciences or related degree Exp: 1-2 years |
The Multiplex Assays Development team is growing, and we are looking for a highly motivated Senior Research Associate who is passionate about collaborating with a team of scientists to develop and commercialize complex novel technologies for visualizing biology. A successful candidate will have the opportunity to independently prepare and maintain an inventory of reagents and buffers in order to perform multiplex immunofluorescence experiments, analyze data, and communicate results to the team. This cross-functional, team-oriented position requires strong organizational skills, exceptional attention to detail, and robust scientific communication skills. | 2/9/2023 |
| 5264 | Cell Signaling Technology Danvers, MA Research Associate I Bachelors in Biological Sciences (Biochemistry, Biotechnology or related discipline). Exp: 1 year |
The Custom Conjugation team is growing, and we are looking for a highly motivated Research Associate. The main responsibility of this position is the conjugation of antibodies to fluorescent dyes, oligonucleotides, beads, HRP, biotin, PE, PE tandem dyes and utilization of the following techniques: protein purification and determination, western blotting and immunoprecipitation. | 2/9/2023 |
| 5265 | Cell Signaling Technology Beverly, MA Lab Technician II BS/BA Degree in Chemistry or related science Exp: 0-2 years |
The Lab Technician II Buffer Prep is primarily responsible for following standard operating procedures, with increasingly limited supervision and as part of a team, to provide high quality chemical solutions, highly responsive service and to perform a wide variety of basic laboratory tasks in support of CSTs Production, Development, and Research laboratories. | 2/9/2023 |
| 5266 | Civetta Therapeutics Cambridge, MA Cell Biology Research Associate BS in Biology, Molecular Biology, Biochemistry, or related Life Science discipline Exp: 1-3 years |
We are seeking a highly-motivated Research Scientist to help support our chemical biology efforts at Civetta. This candidate will help us discover small molecule modulators of beta-propeller proteins, support validation of new targets, and help propel our ongoing drug discovery programs. This is an excellent opportunity for individuals looking to work in a fast-paced, dynamic biotech environment. | 2/9/2023 |
| 5267 | WuXi Apptec Plainsboro, NJ Associate Scientist I Bachelor’s degree in chemistry, biology, or a related discipline Exp: 0-2 years |
The Associate Scientist I will be primarily responsible for the bioanalysis of samples at WuXi AppTec and will follow validated or experimental bioanalytical procedures, to perform assays and support pharmaceutical product development, testing and evaluation in a GLP regulatory laboratory environment. The employee will use state-of-the-art technologies/techniques to perform top-quality sample analysis and testing for key pharmaceutical and biotech clients across the industry. | 2/9/2023 |
| 5268 | WuXi Apptec San Diego, CA Research Associate II - In Vivo Pharmacology Master degree in Molecular and Cell Biology or Bachelor degree Exp: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 2/9/2023 |
| 5269 | WuXi Apptec Cranbury, NJ Associate Scientist I - PKPD Bachelor’s degree in animal science, biology, or a related discipline. Exp: 0-3 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC standards. | 2/9/2023 |
| 5270 | Catamaran Bio Boston, MA Research Associate / Senior Research Associate, Cell Culture BS or certificate in biology, biotechnology, or equivalent/related disciplines. Exp: 1-5 years |
Catamaran is seeking an experienced, hands-on Research Associate / Senior Research Associate to support Catamaran’s development of an allogeneic NK cell drug product. The successful candidate will be responsible for generating and maintaining stocks of cell lines used for in vitro and in vivo assays, including feeder cells, tumor cell lines, NK cells and genetically modified cells. This work involves cell isolation, expansion, engineering, harvest and cryopreservation. This role will require collaborating extensively with Research and CMC teams. The ideal candidate has relevant experience in cell culture of primary human cells and cell lines, and is excited to join a small, fast-paced team with a “can-do” attitude to drive forward our new cell therapy platform. | 2/9/2023 |
| 5271 | Catamaran Bio Boston, MA Research Associate/Senior Research Associate, Cell Process Bachelors or master’s degree in chemical engineering, immunology, biology, synthetic biology, chemical biology, biochemistry, pharmaceutical sciences, Exp: 0-2 years’ |
The Cell Process Team is seeking a talented, diligent, and collaborative research associate to execute and design cell expansion process activities for the advancement of our best-in-class CAR-NK Cell Therapies for Oncology and other diseases. Cell Process works to ingeniously solve the challenges associated with the allogeneic manufacture of CAR-NK cell therapies including cell isolation/enrichment; cell engineering and gene editing; and cell expansion. They will be responsible for the operation of a clinical-scale bioreactor process design for the expansion of clinical CAR-NK candidates, execution of cell-based assays for in-process characterization, and technical process transfer to internal and external manufacturing sites in support of Phase 1 clinical activities. The ideal candidate is a self-motivated and technically competent process development scientist or engineer with an interest in bioreactor design and control, who is excited to join a small, fast-paced team with a “can-do” attitude to drive forward our new cell therapy platform. This is a unique opportunity to realize the promise of allogeneic cell therapy manufacturing paradigms and bring the TAILWIND platform to life at a clinical scale. | 2/9/2023 |
| 5272 | Cellics Therapeutics San Diego, CA Research Associate, Quality Control (Biologics)– San Diego BS/BA in chemistry, biology, or a related field is required, advanced degrees a plus. Exp: 1-3 years |
Cellics Therapeutics is seeking a Research Associate of Quality Control, reporting to the Director of Analytical Development and QC, to conduct quality control testing of incoming raw materials, in-process, release and stability samples for biologics drug intermediates, drug substances, and drug products. The candidate also performs the environmental monitoring for manufacturing facilities | 2/9/2023 |
| 5273 | Charter Medical Winston-Salem, NC Quality Engineer Bachelor of Science degree in technical field (life science, physical science, engineering or related field) required. Exp: 1-3 years |
Conducts investigations and Root Cause Analysis derived from Customer Complaints, CAPAs, Trending, Out of Specifications, Nonconformances, etc. Interfaces with customers to provide reports, data and/or technical support for Products, Complaints, Change Control and Customer Notifications. Develops and monitors implementation of Protocols for product evaluation as required. Creates, edits and/or revises Test Method Validations, SOPs, WIs, Product Specifications as required. Performs Supplier Quality Audits, SCARs (Supplier Corrective Actions) as well as Notifications issuance. Assists with Corrective Action system, including but not limited to, administrative duties for database maintenance, serve as CAPA team member or CAPA team leader, facilitate root cause analysis with CAPA teams, ensure CAPA documentation is complete and accurate, perform follow-up evaluation of CAPA effectiveness, and provide trending reports. Addresses Customer Complaints, derived investigations, corrective actions implementation, and reporting. Assists with hosting, preparing and coordinating external audits and/or Technical Visits as requested. | 2/9/2023 |
| 5274 | Cogent Professionals Indianapolis, IN Experienced Pharmaceutical Analytical Chemist MS - Chemistry Exp: 1-3 years |
We currently have a role available for an Experienced Pharmaceutical Analytical Chemist. Job duties include, but are not limited to: Purification using one or more of the following: Normal phase purification using Teledyne ISCO Combiflash and/or Torrent systems Normal phase method development using TLC Reversed phase purification using Teledyne ISCO Combiflash, ACCQ Prep, and EZ Prep flash/HPLC systems Reversed phase purification using Agilent 1100/1200/1260/1290 series Chiral purification using LC and SFC systems Familiarity with ChemStation. Perform instrument maintenance and troubleshooting as needed. | 2/9/2023 |
| 5275 | Debut Technology San Diego, CA Fermentation Technician College-level coursework in general biology, microbiology, and chemistry is preferred Exp: 1-4 years |
The Fermentation Technician will be a critical contributor to our research and production teams by performing various lab support duties. The role requires multiple hands-on tasks, including cleaning and autoclaving glassware and small equipment. | 2/10/2023 |
| 5276 | Decipher Biosciences San Diego, CA Clinical Lab Technician Bachelor’s degree required Exp: 1 years’ |
The Clinical Lab Technician’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. | 2/10/2023 |
| 5277 | Decipher Biosciences San Diego, CA Research Associate I, Assay Development B.Sci. in biological sciences (or related field) Exp: 1-2 years |
The Research Associate I will support the Assay Development team at Decipher Biosciences; assisting in research, development, and optimization of genomic assays, and supporting general laboratory maintenance and document control. Other responsibilities might be applied as needed. | 2/10/2023 |
| 5278 | Deepcell Menlo Park, CA Research Associate/Senior Research Associate, System Integration Bachelor’s or Master’s degree in Bioengineering, Biomedical Engineering, or similar subject is required, Exp: one year |
Operate and maintain lab instruments, including Deepcell R&D systems; Troubleshoot and optimize components related to Deepcell’s proprietary platform; Perform cell culture protocols. Improve and develop SOPs with consistency and clarity; Execute standard molecular biology techniques; Perform routine laboratory maintenance activities | 2/10/2023 |
| 5279 | Astellas Seattle, WA Research Associate II, Process Development in Seattle, Washington MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Process Development is to execute experiments to improve clinical-grade, gene-editing processes of Universal Donor Cells and to provide data for CMC documents. This Research Associate II role will work as part of a team evaluating processes, and planning/executing experiments to evaluate all aspects of culturing, gene-editing, and processing of pluripotent stem cells. This position will be provided training to perform all required fundamental skills. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 1/30/2023 |
| 5280 | Astellas Seattle, WA Research Associate II, Cell Analytics in Seattle, Washington MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the molecular engineering and characterization for our gene edited Universal Donor Cells, by utilizing various cell culture techniques. They will work as a key member on a fast paced team to culture pluripotent stem cells as well as run cellular assays to characterize our proprietary Universal Donor Cells. | 1/30/2023 |
| 5281 | Astellas Westborough, MA Research Associate II, Analytical Development in Westborough, Massachusetts MS Exp: 0-2 years |
The Research Associate will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOPs, and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 1/30/2023 |
| 5282 | Astellas South San Francisco, CA Research Associate II, Vector Biosciences in South San Francisco, California Master's Degree in Molecular Biology, Cell Biology, Life Sciences Exp: 1+ years |
We are looking for a highly motivated Research Associate to join the Vector Biosciences Group in our South San Francisco R&D labs. This position involves application of multidisciplinary experiments including molecular cloning, cell culture, AAV packaging and purification and other in vitro experiments. | 1/30/2023 |
| 5283 | Astellas South San Francisco, CA Research Associate I/II, Vector Biosciences in South San Francisco, California Master's Degree in Molecular Biology, Biology, Life Sciences or a related discipline Exp: 1+ years |
The Research Associate will support the Vector Biosciences team and assist with the development of novel AAV gene therapy vectors using molecular biology techniques. The Research Associate will be located in our South San Francisco R&D laboratories. | 1/30/2023 |
| 5284 | Astellas Seattle, WA Research Associate II, Clinical Gene Editing in Seattle, Washington MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 1/30/2023 |
| 5285 | Atsena Therapeutics Durham, NC Laboratory Operations Assistant Bachelor’s degree Exp: 1 year |
We are seeking an enthusiastic, highly motivated Lab Operations Assistant to support our company’s growth. The successful candidate will bring experience, knowledge, and best practices and serve as primary backup to the Laboratory Operations Manager to oversee inventory, shipping/receiving, vendor & equipment service calls and general facility oversite. Additionally, this person will provide basic laboratory support to the science teams. We recently moved into a state-of-the-art facility, and this is a great opportunity for building up the function from the ground level. | 1/30/2023 |
| 5286 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters Exp: Entry Level for level I, |
The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. | 1/30/2023 |
| 5287 | Avid Bioservices Tustin, CA Biomanufacturing Associate Downstream Purification (Flex Team) Bachelor's degree in a life science field such as Biology or Biotechnology (REQUIRED) Exp: 1+ years |
As a Biotech Manufacturing Associate, you play an integral role in ensuring the on-time delivery of quality biopharmaceutical products. You get to participate in a variety of tasks including purification of biologics, keeping up-to-date GMP documentation, writing reports, ordering materials, and scheduling equipment services. You are conscientious about maintaining strict compliance with GMP manufacturing practices as you adhere to our standard operating procedures. | 1/30/2023 |
| 5288 | Axial Therapeutics Woburn, MA RESEARCH ASSOCIATE/SENIOR RESEARCH ASSOCIATE - BIOSCIENCES Bachelor’s degree in biology, biochemistry, or a related field preferred Exp: 1-3 years |
In this role the Research Associate will support biology as a member of a highly matrixed drug discovery team and will be responsible for the execution and troubleshooting of various cell-based and biochemical assays and experiments. The Research Associate will contribute to drug screening and mechanism-of-action studies for projects in immuno-oncology and neurological diseases and disorders and have opportunities to contribute to new target discovery and validation. This proactive researcher will collaborate with team members, identify opportunities to improve efficiency, share ideas and expertise and contribute to Axial’s creative, dynamic, and collaborative culture. | 1/31/2023 |
| 5289 | Azzur Devens, MA Microbiologist Bachelors of Science or Bachelors of Arts in the field of the life sciences. Masters of Science preferred. Exp: 1-2 years |
Azzur Lab is looking for Microbiologist, who will perform laboratory testing and interacts with clients to interpret their results. The Senior Microbiologist has the responsibility to ensure that laboratory testing is completed in accordance with established methods and protocols. | 1/31/2023 |
| 5290 | Beam Therapeutics RTP, NC Manufacturing Associate (multiple openings) BS, MS a plus, in Life Sciences or Engineering Exp: 0-5 years |
Beam is expanding our geographical footprint to RTP, NC with the recent announcement of a 100,000 square foot manufacturing facility in addition to our laboratory-based facilities located in Cambridge, MA. We are looking for highly energetic Manufacturing Associates to support start-up and scaling of cGMP manufacturing at our new RTP site. Reporting to the Manager of Manufacturing, the successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and start-up. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment. | 1/31/2023 |
| 5291 | Berkshire Sterile Manufacturing Lee, MA Process Engineering Associate Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science Exp: one (1) year |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 1/31/2023 |
| 5292 | Biocoat Horsham, PA Chemistry Production Technician Bachelor’s degree in Chemistry or similar science-related field is preferred. Exp: 1 year |
Biocoat is a global leader in manufacturing, applying, and developing hydrophilic coatings for medical devices. Our team needs a Chemistry Production Technician! The technician will perform manufacturing operations for medical device coating products according to Good Manufacturing Practices, ISO requirements, and appropriate regulatory agencies. | 1/31/2023 |
| 5293 | Biomere Richmond, CA Research Associate (Small & Large Animal) AS or BS Degree in Science (or equivalent degree) preferred. Exp: RA I: 1 or 2 years |
Research Associate works under the direct guidance of the Site Head and the general guidance of the senior staff. Research Associate is proficient in animal procedures/animal husbandry, grant, internal, and/or contract research studies according to the study protocols and to the company guidelines and standard operating procedures (SOPs). | 1/31/2023 |
| 5294 | Boston Analytical Salem, NH Analytical Chemist II Bachelor’s degree in Chemistry or a related discipline is required Exp: 1+ years |
The Analytical Chemist II conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 2/1/2023 |
| 5295 | Boston Analytical Salem, NH Analytical Chemist I - Nitrosamines Bachelor’s degree in Chemistry or a related science discipline Exp: 0-2 years |
The Analytical Chemist in the nitrosamines laboratory conducts routine screenings of samples for a range of nitrosamine compounds according to FDA, USP, cGMP, and Boston Analytical Inc. Standard Operating Procedures. Duties will include preparation and nitrosamines screening analysis of drug products, APIs, and raw materials using GC-MS and LC-MS. | 2/1/2023 |
| 5296 | Boston Analytical Framingham, MA Microbiologist EM FTE BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Environmental Monitoring Microbiologist conducts cleanroom monitoring activities to ensure the air, surfaces, and critical utilities utilized for pharmaceutical product manufacturing meet cGMP requirements. These samples are collected according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. | 2/1/2023 |
| 5297 | Boston Analytical Salem, NH Microbiologist - Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 2/1/2023 |
| 5298 | Boston Institute of Biotechnology Southborough, MA Research Associate / Scientist / Sr. Scientist – Downstream Process Development Bachelor’s degree in Biology or Chemistry related field; MS degree in Biochemistry or Chemical Engineering. Exp: BS: 0-10 years; MS: 0-5 years |
Essential requirements for this position include in-depth understanding and hands-on experience with recombinant protein purification from different expression hosts (including E. coli, Yeast, CHO and HEK) and an aptitude for careful, detail-oriented experimentation. The level of the position will be commensurate with the candidate’s experiences. | 2/1/2023 |
| 5299 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 2/2/2023 |
| 5300 | Cabaletta Bio Philadelphia, PA Associate Scientist/Scientist, MSAT M.S. Exp: 1 + years’ |
The MSAT/Process Development group is seeking a motivated Associate Scientist/Scientist, MSAT who will be responsible for directing cell therapy product candidates through cGMP process development. This position will interact with internal and external partners and require up to 10% domestic travel, as well as occasional weekend and overtime work. | 2/2/2023 |
| 5301 | Bristol-Myers Squibb Redwood City, CA Associate Scientist, In Vivo Pharmacology, Tumor Microenvironment Research Master’s Exp: 0-3+ years |
You will execute in vivo studies, analyze, and present data. You will gain and provide technical and scientific in vivo pharmacology expertise to advance drug discovery programs from target identification/validation to IND enabling activities. You will interact and collaborate effectively in a multi-functional dynamic team environment. | 2/2/2023 |
| 5302 | Bristol-Myers Squibb Devens, MA Associate, QC Microbiology, Cell Therapy Bachelor’s degree required, preferably in the life sciences. Exp: 0-2+ years |
Bristol Myers Squibb is seeking a QC Associate to join our QC Microbiology team at the Cell Therapy Facility (CTF) in Devens, MA. The QC Associate is responsible for supporting Quality Control microbiological in-process, release, and stability testing of clinical and commercial cell therapy drug product. Additionally, the QC Associate will support clean utilities systems testing, environmental monitoring within the manufacturing environment, and may assist with investigations and continuous improvement efforts. The QC Associate role is stationed in Devens, MA and reports to the Manager, QC Microbiology for the Devens CTF. | 2/2/2023 |
| 5303 | Bristol-Myers Squibb Devens, MA QC Associate Microbiology, Cell Therapy Bachelor’s degree required, preferably in the life sciences. Exp: 0-2+ years |
This position offers a $3,500 sign on bonus (external candidates only) The Integrated Genetics Division of LabCorp is seeking a Molecular Technologist to join their Molecular Diagnostics team in Westborough, MA! The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, real time PCR, Sanger Sequencing and Southern Blot analysis to test for specific genetic diseases such as cystic fibrosis, spinal muscular atrophy and Fragile X syndrome to name just a few. The schedule for this position will be: Sunday – Thursday (7:00am – 3:30pm) | 2/2/2023 |
| 5304 | Covance Westborough, MA Molecular Laboratory Technologist Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology Exp: 1 year |
LabCorp is seeking a Data Analyst for our Genomics department to join our team of clinical laboratory professionals in Westborough, Massachusetts! The Data Analyst team is responsible for analyzing data generated from clinical molecular laboratories in Research Triangle Park, NC and in Westborough, MA. The team has primary expertise in analyzing sequencing data from next-generation, exome, and Sanger assays, and additional expertise in analyzing copy number data from MLPA and microarray. The team works closely with the laboratory and the clinical directors to ensure high quality results are provided to patients. The schedule for this position is Monday – Friday, 8:30 a.m. – 5:00 p.m. | 2/2/2023 |
| 5305 | Covance Westborough, MA Laboratory Data Analyst (Molecular Genetics) Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology Exp: 1 year |
The successful candidate will work together with our study directors, veterinarians, and quality assurance department to ensure all study aspects are conducted per scientific and regulatory standards. The hands-on experience we offer in the lab has great possibilities for growth with exposure to all aspects of studies including sample preparation, dosing techniques, and surgery, in many different animal models. Highly motivated individuals will have an advancement track through the department. This position is an integral component of a fast-paced environment. The successful candidate will be selected based on aptitude, experience, and a dynamic personality to join our In-Vivo team. | 2/2/2023 |
| 5306 | Covance Bedford, MA Research Assistant Bachelors in a Life Sciences (i.e. biology, pharmacy, veterinary sciences) Exp: 1 year |
We are currently seeking a highly motivated, quality and detail oriented individual to join our In-Vitro Genetox team. The successful candidate will work closely with our study directors and quality assurance to ensure all study aspects are conducted per scientific and regulatory standards. This position is an integral component of a fast-paced environment. You will be joining a rapidly growing team and will be selected based on both experience/aptitude and a dynamic personality. The work is focused on in-vitro testing of medical devices and pharmaceutical products using Good Laboratory Practices (GLP). The main assays performed are AMES, MLA and Chromosomal Aberration testing. Studies are conducted under OECD and ISO guidelines, protocols, and Standard Operating Procedures. | 2/2/2023 |
| 5307 | Covance Saint Paul, MN 2nd Shift, Afternoons- Clinical Technologist Drug Testing Extractions - Wet Chemistry Bachelor's degree from a four?year college or university in chemical, biological or clinical laboratory science or medical technology Exp: 1 year |
The Clinical Toxicology Extraction Technologist Trainee or Technologist receives on‑the‑job training for the pre‑analytical wet chemistry prep of patient samples in the Clinical Toxicology Laboratory. This laboratory is fast‑paced and performs a variety of high complexity testing including therapeutic drug testing, designer panel drug testing, comprehensive oral fluid drug testing, occupational drug testing, autopsy testing, unknown analysis testing, pharmaceutical testing, and drug confirmation testing on blood, serum, urine, and meconium sample types. This testing uses a variety of wet chemistry extraction techniques including liquid-liquid, solid phase, and dilute-n-shoot methods. These extractions utilize both tubes and 96-well plates via manual or semi-automated pipetting systems which are then analyzed on a variety of instrument and software processing platforms. | 2/2/2023 |
| 5308 | Covance Greenfield, IN Research Assistant I Molecular BioA BS, BA, or AS degree in Chemistry, Biology, Biotech, Microbiology, Cellular Biology or related field. Exp: 0-2 years |
Based on continued growth and planned expansion for the CMC (Chemistry Manufacturing & Controls) team, we have multiple openings for Research Assistant I Molecular BioA. This is an entry level position for candidates with 0-2 years of experience, such as recent or upcoming graduates, who are looking to apply their knowledge in a regulatory laboratory environment. Read more about our CMC area https://drugdevelopment.labcorp.com/services/manufacturing-support.htmlBased on continued growth and planned expansion for the CMC (Chemistry Manufacturing & Controls) team, we have multiple openings for Research Assistant I Molecular BioA. This is an entry level position for candidates with 0-2 years of experience, such as recent or upcoming graduates, who are looking to apply their knowledge in a regulatory laboratory environment. Read more about our CMC area https://drugdevelopment.labcorp.com/services/manufacturing-support.html | 2/3/2023 |
| 5309 | Covance Indianapolis, IN Research Assistant I - BioAnalytical Lab Operations Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1- 2 years |
In this position you will be part of a cohesive team and conduct routine analysis on biological and chemical samples in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines for multiple studies. | 2/3/2023 |
| 5310 | Leidos Biomedical Research San Antonio, TX Research Associate I Bachelor’s degree in biology, microbiology or related field Exp: 1+ years |
The Defense Health Operation of Leidos is currently looking for a Research Associate to join the Expeditionary and Trauma Medicine Department supporting biomedical research at the Naval Medical Research Unit, San Antonio (NAMRU-SA) in San Antonio, TX. NAMRU-SA serves as one of the leading research and development laboratories for the U.S. Navy and conducts gap driven combat casualty care, craniofacial, and directed energy research to improve survival, operational readiness, and safety of Department of Defense (DoD) personnel engaged in routine and expeditionary operations. Members of the Expeditionary and Trauma Medicine Department conduct research focused on the protection, resuscitation, and stabilization of combat casualties at front-line points of care in the combat theater. This includes primary and pre-clinical research for the development and optimization of drug products, advanced therapies for the treatment of hemorrhagic shock and identifying and mitigating stressors through the evaluation of products and agents. | 2/3/2023 |
| 5311 | Leidos Biomedical Research Groton, CT Research Assistant - Psychology / Neuroscience / Biomedical Bachelors in psychology, neuroscience, biomedical engineering, or closely related field Exp: 1+ years |
Leidos is currently accepting applications for a full-time, benefits-eligible Research Assistant position, to assist with research studies, research administration, and laboratory management on the Human System Interaction (HSI) Research Team at the Naval Submarine Medical Research Laboratory (NSMRL) onboard Naval Submarine Base New London, located in Groton, CT. The laboratory delivers research solutions promoting the health, welfare, and performance of undersea warfighters. The position is ideal for an individual seeking to deepen their research experience in preparation for graduate study. | 2/3/2023 |
| 5312 | Leidos Biomedical Research Fort Detrick, MD Research Assistant Bachelor of Science in a related discipline. Exp: 1-2 years |
The Defense Health Operation of Leidos is currently looking for a Research Assistant to support biological research at the Biological Defense Research Directorate (BDRD) within the Naval Medical Research Center (NMRC) in Frederick, MD. The BDRD within NMRC facilitates biological research for the rapid detection of infectious diseases of global importance and the enhancement of global disease surveillance for early pathogen detection and response. | 2/3/2023 |
| 5313 | Eli Lilly Indianapolis, IN Biologist - Diabetes, Islet Biology & New Platforms Bachelor’s Degree in biology, molecular biology, biochemistry or related field Exp: 1 year |
The Diabetes, Islet Biology & New Platforms Group is searching for a hardworking scientist at the Associate level with experience in biochemistry and cellular and molecular biology. The successful candidate will work in a multidisciplinary environment and contribute to the discovery and development of novel therapies for Diabetes. The focus of the work will be to identify and validate novel molecular targets for diabetes treatment, and to develop and implement biochemical and cell based in vitro assays supporting drug discovery efforts. The candidate is expected to have a good knowledge base of pharmacology and cell biology and demonstrate willingness to learn new skills. | 2/3/2023 |
| 5314 | Eli Lilly Branchburg, NJ Quality Assurance Associate - Manufacturing Compliance Bachelors degree or higher in the sciences, engineering, or related field Exp: 1-3 years |
The Quality representative provides support to manufacturing and ensures quality systems and GMP compliance. The QA representative provides assistance and guidance in deviation investigations, change control proposals, procedure and master production batch record revisions, validations, and batch dispositions. The QA representative’s position is essential for maintaining quality systems, ensuring GMP compliance and ensuring an inspection readiness state. | 2/3/2023 |
| 5315 | Eli Lilly Branchburg, NJ Research Associate-Quality Control (QC) Bioassay MS in a science related field (e.g. Biology, Biochemistry, etc.). Exp: 1 year |
Conduct routine and non-routine analyses of in-process materials, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. Perform routine QC responsibilities as needed. Apply acceptable cGMP practices during execution of all work tasks. Work independently with moderate supervisory guidance. | 2/3/2023 |
| 5316 | Eli Lilly Branchburg, NJ Engineer-Reliability BS in Engineering Exp: 1-5 years |
Reliability Engineer is accountable for the equipment reliability and maintenance strategy of the equipment. This is achieved by the continuous monitoring of equipment operational performance and identifying/implementing action needed for improvement. These improvement actions will be a combination of installation set-up, utilization, and maintenance servicing including spare parts, JP/PM, work standardization, etc. Deep understanding of the manufacturing equipment, its processes, and the impact of the processes on the instrumentation/equipment are key to the success of this position. The incumbent will establish many key working relationships to coordinate critical Facilities activities with Quality Control, Quality Assurance, Utility Room, Engineering, and Manufacturing Supervision. Other duties may be assigned at the discretion of the Senior Reliability Engineer. | 2/3/2023 |
| 5317 | Eli Lilly Indianapolis, IN QC Associate - Medical Device Bachelor's degree in STEM discipline Exp: 1 year |
The QC Associate is primarily responsible for assessing, establishing, and supporting quality systems within the Indianapolis Device Manufacturing (IDM) QC organization per applicable Lilly Quality Standards (LQS) and Global Quality Standards (GQS). This role provides daily quality control support, and guidance for the IDM QC Laboratory involving laboratory operations, testing practices, analytical equipment, and test method development impacting the Device Quality Control Laboratory. | 2/3/2023 |
| 5318 | Eli Lilly Indianapolis, IN Engineer - Human Factors MS in Human Factors / Usability Engineering or a related field (e.g., Cognitive Psychology, HCI, Biomedical Engineering, Industrial Engineering, Mecha Exp: 1+ years |
We are seeking an experienced Senior / Principal Human Factors Engineer with an advanced understanding of perceptual, cognitive, and ergonomic theories and principles, and the ability to apply this knowledge to the conceptualization, design, and evaluation of medical devices and digital health systems. The role requires effective collaboration with multidisciplinary team leadership; to work with colleagues from design, engineering, medical, marketing, quality, manufacturing and regulatory to apply human-centered design methods through implementation of usability processes, determination of desired user profiles and environments, development of user documentation, and creation of usability files. | 2/3/2023 |
| 5319 | Alexza Pharmaceuticals Mountain View, CA QC Analyst I/II/III (Temp) Bachelor’s Degree in science or related field Exp: Level I: 0-2 years |
Provide timely analyses to support manufacturing and stability. Primary responsibilities include but not limited to physical testing of components and raw materials, in process and release of commercial product or clinical supplies Independently perform assays under GMP, maintaining data integrity and ensuring compliance with company SOPs and specifications. Provide accurate, written documentation of all work, including detailed observations and conclusions. Under general guidance, participate in laboratory investigations Independently operate, maintain and troubleshoot laboratory instrumentation and equipment in a safe working environment | 1/23/2023 |
| 5320 | Nitto Denko Avecia Cincinnati, OH Quality Assurance Specialist BS/BA in science Exp: 1-3 years |
Acts as departmental resource for cGMP programs, Writes SOP’s compliance documents for cGMP program. Reviews and authorizes batch production records and quality control documentation. Performs compliance audits of suppliers, contract labs and vendors then writes audit reports. Performs internal audits and ensures observations are corrected. Sets-up and tracks material flow and material-labeling process to ensure compliance with cGMP program. Trains staff in area of cGMP and maintains training records. | 1/23/2023 |
| 5321 | Avidity Biosciences San Diego, CA RESEARCH ASSOCIATE B.S./B.A./M.S degree in biological sciences Exp: 1-4 years |
As Avidity advances programs into the clinic, an effective quality control strategy will be critical to ensuring reproducibility of our drug substance. We are seeking a Research Associate to join the Analytics group with experience in mammalian cell biology and/or molecular biology to assist with the development of mammalian cell-based potency assays for late phase drug product release. | 1/23/2023 |
| 5322 | Avidity Biosciences La Jolla, CA RESEARCH ASSOCIATE, IN VIVO PHARMACOLOGY B.S./M.S. in Molecular Biology, Physiology, Pharmacology, or related disciplines Exp: 1-2 years |
We are seeking a highly motivated Research Associate I/II to join our biology team responsible for the preclinical development of drug compounds. Successful candidates will bring hands-on experience in rodent disease models, PD, and PK studies. This is a lab-based position primarily performing, hands-on, in vivo studies in rodents, in vitro work, analyzing data, meeting with key stakeholders to present results, and serving as a team representative. The ideal candidate will be proficient in biological and physiological techniques (in vitro and in vivo), precise documentation, demonstrate clear and professional verbal and written communication, and be a strong team player. | 1/23/2023 |
| 5323 | Avidity Biosciences San Diego, CA SR. RESEARCH ASSOCIATE/ASSOCIATE SCIENTIST B.S./B.A./M.S degree in biological sciences Exp: 1-4 years |
Avidity is seeking an enthusiastic and dedicated Sr. Research Associate/Associate Scientist to join our Discovery Biology team who can assist with ongoing studies that aim to expand our AOC platform. This is a hands-on research position, and a successful candidate will have a proven record of producing exceptional results in a laboratory setting. | 1/23/2023 |
| 5324 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc in cell biology or similar discipline. Exp: 1 to 6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 1/23/2023 |
| 5325 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 1/24/2023 |
| 5326 | CRISPR Therapeutics Boston, MA Research Associate II, mRNA in vivo MS degree in Chemistry, Chemical Engineering, Analytical Chemistry, Biochemistry, Bioengineering, Pharmaceutical Sciences or related field Exp: 0-3 years |
CRISPR Therapeutics is seeking a highly motivated Research Associate to join our In Vivo Technical Operations department in Boston, Massachusetts. The incumbent will be responsible for the mRNA synthesis and purification optimization to establish process for large-scale mRNA manufacturing. This position will also support therapeutic programs in multiple disease areas in R&D department as well. Prior experience in mRNA synthesis, purification and characterization is desired. | 1/24/2023 |
| 5327 | CRISPR Therapeutics Boston, MA Research Associate II/Senior Research Associate, Toxicology RA II: MS in biology or related disciple Exp: 0‒2 years |
We are seeking a Research Associate II/Senior Research Associate to build our capabilities within our In Vivo Pharmacology team. The successful candidate will be responsible for implementation of in vivo studies involving mice and rats. The candidate should be proficient handling, administering test article, and sample collection from both species. The candidate will work on all aspects of implementing in vivo studies: design, administration, in-life observations, postmortem analysis, report generation, and data presentation. The In Vivo Pharmacology team interacts with most of the research groups within CRISPR, offering the candidate exposure to a variety of different programs and platforms. | 1/25/2023 |
| 5328 | NorTech Life Sciences Blue Earth, MN Project Engineer Bachelor's degree (BS) from four-year college or university Exp: 0+ years |
Introduce new products into manufacturing and service. Determines engineering and design requirements; resolves engineering problems; verifies and maintains project time lines; meets cost standards; evaluates manufacturing systems applications; confirms systems and components capabilities; develops manufacturing processes and standards; assures product quality; prepares technical product reports. May develops manufacturing methods, systems and processes to produce a high-quality product at optimal cost for new product introduction. | 1/25/2023 |
| 5329 | Physical Sciences Boston, MA CHEMICAL ENGINEER BS or MS degree in Chemical Engineering, Chemistry or Materials Science Exp: 0 to 2 years’ |
Physical Sciences Inc., located just north of Boston, in Andover, is seeking a Chemical Engineer with a strong background in reaction kinetics, heat and mass transfer, and separations. We are seeking an applicant who can assist with developing and scaling-up materials production from laboratory/batch processes to pilot-scale/continuous processes. The applicant we seek would ideally have materials synthesis, purification and characterization experience. We are looking for a strong worker, who can safely and effectively execute on their ideas as a member of a team and sometimes as an individual contributor. This individual will play a key role in growing a diverse portfolio of technologies funded by the DoD, DoE, and NASA, in areas such as firefighter decontamination, atmospheric water harvesting and microreactor technology development. | 1/25/2023 |
| 5330 | Physical Sciences Boston, MA CHEMICAL ENGINEER/CHEMIST Bachelors or Masters in Chemistry, Chemical Engineering, Physics, Applied Physics, Material Science or related field is required. Exp: Entry-level |
Physical Sciences Inc., located just north of Boston in Andover, seeks well-qualified candidates for positions on our research and manufacturing team. This position is intended for an individual who is interested in supporting and leading programs devoted to the development and manufacturing of products that employ active photonic materials. An ideal candidate should be interested in a career devoted to applied research and product development with strong experimental, hardware, and leadership skills, and should be interested in maturing technologies and manufacturing processes from concept to prototype. | 1/25/2023 |
| 5331 | Tanvex BioPharma San Diego, CA QC Associate, Lab Control & Raw Material - #1346 Bachelor’s degree or advanced degree in chemistry, biology, biochemistry or related life sciences discipline. Exp: 0-3 years’ |
The Quality Control Associate, Lab Control & Raw Materials is responsible for conducting routine and non-routine analyses of raw material and GMP product as assigned using appropriate analytical methods. This position will coordinate sampling, shipping, and testing of raw materials at outside contract laboratory and in-house to ensure data integrity and compliance, and will work with internal departments to ensure timely testing of raw materials for Manufacturing. | 1/26/2023 |
| 5332 | Tanvex BioPharma San Diego, CA Research Associate, Cell Culture Process Development - #1358 BS or advanced degree in chemical/biochemical engineering, cell biology, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Cell Culture Development is responsible for executing individual experiments related to all aspects of cell culture process development of biopharmaceuticals, including media preparation, bioreactor setup, cleaning, sterility and operation, maintaining instruments and equipment, examining data and preparing experiment reports. Applies basic engineering and scientific principles to perform trouble-shooting of processes, instrumentation, and equipment. | 1/26/2023 |
| 5333 | Tanvex BioPharma San Diego, CA Research Associate, Bioassay Development - #1438 BS or advanced degree in cell and/or molecular biology, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Bioassay Development is responsible for biological characterization of Biologics drug candidates including method development, method qualifications, method transfer and training, and routine non-GMP sample testing. Designs, executes and documents a set of experiments that contribute to project objectives. | 1/26/2023 |
| 5334 | Tanvex BioPharma San Diego, CA Manufacturing Associate, Downstream Bachelor's or advanced degree in life sciences or related discipline Exp: 0-3 years |
Under general supervision, the Manufacturing Associate, Downstream, will perform routine manufacturing activities in GMP manufacturing areas including purification and the associated sub-processes/ preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Perform manufacturing steps, execute routine batch records, and revise documents such as batch records and SOPs as needed. Flexible shift schedules and overtime may be required. | 1/26/2023 |
| 5335 | Tanvex BioPharma San Diego, CA Research Associate, Analytical Chemistry Development BS or advanced degree in chemical/biochemical engineering, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Analytical Chemistry Development is responsible for providing analytical chemistry support to research, process development, product development and manufacturing of biological therapeutics. Participate in analytical method development, characterization, qualification, validation as well as method transfer. Perform various analysis for characterization of biological therapeutics. | 1/26/2023 |
| 5336 | UniQure Lexington, MA QA Specialist I Bachelor’s degree in Life Sciences or Engineering Exp: 1-3 years |
The Quality Assurance Specialist I supports the day-to-day quality operations via Manufacturing Clean Room presence, Material/Inventory QA Release, oversight of all elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), investigations, change control, batch review, data integrity, and training in support of biologics manufacturing production. | 1/26/2023 |
| 5337 | UniQure Lexington, MA QC Analyst BA or BS in Chemistry/Biology or other related science Exp: 1-6 years |
The QC Analyst will be responsible for GMP routine/nonroutine QC testing of our AAV-based products and the raw materials/starting materials used according to SOPs. This position supports the second shift at uniQure’s state of the art facility in Lexington, MA. | 1/26/2023 |
| 5338 | Advanced BioScience Labs Rockville, MD QC Microbiology I - (00325_COMPANY_1.5) Bachelor’s degree Exp: 1-2 years’ |
The Quality Control Microbiologist will have several responsibilities in the Quality Control Group. The Analyst will perform environmental monitoring (EM) for particulates and viable samples in support of cGMP manufacturing. This includes several production suites of EU Grade A to D in a GMP facility that produce biopharmaceuticals (vaccines, biologics, viral vaccines, monoclonal antibodies, etc.) In addition, monitoring of purified water, and compressed gases systems is required. Additional responsibilities may include EM data review and compilation and verification of data, report writing and trending of data, gowning training and annual gowning qualification. | 1/26/2023 |
| 5339 | Abenza Bristol, PA Associate II – Quality Control Sample Coordinator Bachelor’s degree in Scientific discipline Exp: 1+ years |
The QC Sample Coordinator Associate II performs incoming and outgoing sample management for in process, release and stability studies. This role is also responsible for reference standard inventory and reconciliation to support all laboratory testing. Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements. Ensure samples are delivered in line with organizational standards, protocol specific requirements and client expectations. Travel between Abzena sites (Bristol PA, San Diego CA and Sanford NC) as needed. | 1/26/2023 |
| 5340 | Advanced Cell Diagnostics Austin, TX Research Associate Bachelor’s degree in biology, chemistry, biomedical engineering, or related field is required. Exp: 1-3 years |
Asuragen is seeking an outstanding BSc-level scientist to join our Research group. This is a full time position focused on developing innovative nucleic acid or protein-based technologies. This role will support new product initiatives to enable novel, multiplexed-PCR technologies that can resolve multiple classes of DNA/RNA markers or proteomics through integration of reagents, instrumentation, analysis algorithms and software. Platforms used in our laboratory include quantitative real-time PCR, digital PCR, capillary electrophoresis, next-generation and long-range sequencing. | 1/27/2023 |
| 5341 | Adesis Wilmington, DE Purification Chemist Bachelor of Science in Chemistry or other relevant field Exp: 1-2 year |
Responsible for assisting chemists in performing various purifications of target compounds in a fast-paced research environment. Purification techniques include, but are not limited to preparative high performance liquid chromatography (prep HPLC), normal phase and reverse phase chromatography, and recrystallization. | 1/27/2023 |
| 5342 | Agenus Lexington, MA Associate Scientist/Scientist I, Analytical Sciences, Mass Spectrometry Master in analytical chemistry Exp: 1-3 years |
An enthusiastic Associate Scientist / Scientist I, ideally with large/complex and small biomolecule analytics expertise in Mass Spectrometry, to join our Mass Spectrometry team as a potential subject matter expert with the goal to oversee and support the characterizations of Agenus therapeutic protein pipeline at various stages. | 1/27/2023 |
| 5343 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Associate I Bachelors in a science or engineering discipline preferred. Exp: zero to two (2) years |
We are currently seeking a Drug Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 1/27/2023 |
| 5344 | Ajinomoto Bio-Pharma Services San Diego, CA Lab Systems Analyst Bachelor’s degree preferred in a Life Sciences discipline, IT, or equivalent preferred. Exp: 0-2 years |
We are currently seeking a Lab System Analyst to support lab systems for Analytical Technologies and Quality Control at Ajinomoto Bio-Pharma Services. This includes supporting one or more of the following: Benchtop lab equipment and computers, LIMS, ELN, MODA, CPMS, chromatography data system (CDS), equipment life cycle management, and data integrity. The Lab Systems Analyst may also perform routine maintenance and repair of the quality lab systems according to standard operating procedures. | 1/27/2023 |
| 5345 | Ajinomoto Bio-Pharma Services San Diego, CA Manufacturing Associate I Formulations 2nd Shift Bachelor’s degree in a Life Sciences discipline or equivalent preferred. Exp: Zero to two (0-2) years |
We are currently seeking a Drug Product Formulations Manufacturing Associate I who is responsible for execution of routine production and manufacturing procedures to support processes and ensure compliance with regulatory requirements. The Manufacturing Associate I will work with the Drug Product team to ensure the successful completion of various cGMP activities. The Manufacturing Associate I will learn and demonstrate proficiency in both the technical aspects as well as the quality systems which govern cGMP manufacturing. | 1/27/2023 |
| 5346 | Ajinomoto Bio-Pharma Services San Diego, CA Microbiology Technician - 1st Shift Bachelors degree preferred in a Life Sciences discipline or equivalent. Exp: Zero to two (0-2) years |
We are currently seeking an Microbiology Technician to support Ajinomoto Bio-Pharma Services manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 1/27/2023 |
| 5347 | Ajinomoto Bio-Pharma Services San Diego, CA Microbiology Technician - 2nd Shift Bachelor’s degree preferred in a Life Sciences discipline or equivalent. Exp: Zero to two (0-2) years |
Microbiology Technician – 2nd shift will support Ajinomoto Bio-Pharma Services manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. You will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 1/27/2023 |
| 5348 | American Regent New Albany, NY R&D Associate Scientist 1- Formulation Development B.S. in Pharmaceutical Science, Chemistry, Chemical Engineering or equivalent required. Exp: B.S.: 0-3 years; M.S.: 0-1 year |
Responsible for formulation and process development activities associated with parenteral drug product development. Participates in scale-up of manufacturing process. | 1/27/2023 |
| 5349 | Ampac Analytical Rancho Cordova, CA Process Engineer Bachelor's of Science Degree in Chemical Engineering required. Exp: One to three years |
We are looking for enthusiastic Chemical Engineers to join our Process Engineering Team! We have several opportunities at our Rancho Cordova, CA location (Greater Sacramento Area). We will pay for your relocation!! | 1/27/2023 |
| 5350 | Ampac Analytical Rancho Cordova, CA Technical Operations Lead I bachelor's degree Exp: 0-1 years |
The position provides continuous technical support and guidance for plant operations. This role provides rapid technical response to issues employing manufacturing techniques to solve problems. This position must have a good understanding of production priorities and will direct production activities accordingly to maximize labor efficiency. This role is responsible for daily activities of production area to ensure that volume, cost, and quality standards are achieved. Work is moderately supervised. Follows specific, detailed instructions. | 1/27/2023 |
| 5351 | Ampac Analytical Rancho Cordova, CA Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Exp: One (1) to two (2) years |
We are looking for enthusiastic Chemists to join our QC Team in Rancho Cordova (Greater Sacramento area)! | 1/27/2023 |
| 5352 | Ansa Biotechnologies Emeryville, CA Manufacturing Associate, Protein Downstream Process Bachelor’s/Master’s Exp: 0-2 years |
Implementing a robust protein production pipeline will be instrumental in providing the key reagents needed to implement the fastest, cleanest, and most accurate DNA synthesis system in the world. As a Manufacturing Associate in the Protein Production team, you will have the exciting opportunity to transition our protein production from research to pilot scale and beyond. You’ll have the exciting opportunity to learn the ins and outs of research and pilot scale recombinant protein purification. | 1/27/2023 |
| 5353 | Arbor Biotechnologies Cambridge, MA Research Associate, CRISPR Early Discovery Bachelor’s degree in biology, biochemistry, molecular biology, or a related field Exp: 1-3 years |
Arbor Biotechnologies is seeking a Research Associate to join our CRISPR Early Discovery team to aid in the earliest stages of discovery and characterization of new gene editing systems. The ideal candidate will have an appetite for learning a wide variety of topics, is self-motivated, and thinks critically about experimental design. | 1/27/2023 |
| 5354 | Arbor Biotechnologies Cambridge, MA Research Associate/Senior Research Associate, Non-Viral Gene Therapy BS/MS or equivalent in Chemical/Biomedical/Biochemical Engineering, Bioengineering, Chemistry, Biochemistry, Pharmaceutical Sciences or a related fiel Exp: 1-3 years |
The Senior Research Associate/Research Associate will support our LNP formulation pipelines and in vitro/in vivo preclinical requirements through the design and execution of experiments to help screen and produce various non-viral formulations enabling the encapsulation of various RNA entities. This candidate will also support various biophysical characterization assays commonly used in nanomedicine. The ideal candidate for this position will be a motivated and proactive individual with a passion for LNP and other nanoparticle formulations and processes. The applicant should have strong wet laboratory, communication and collaboration skills preferably with a background in the appropriate formulation deliverables. This role will have no supervisory responsibilities and will report to the Principal Scientist, Non-Viral Gene Therapy. | 1/27/2023 |
| 5355 | Arbor Biosciences Ann Arbor, MI Lab Technician, NGS team Bachelor’s degree involving molecular biology laboratory work and /or relevant work experience Exp: 6+ months |
This is a role for a talented molecular biologist with experience working with DNA and RNA to perform laboratory experiments as part of our client service offerings. The Laboratory Technician will have project management responsibilities and will be adept at molecular biological bench work. Routine activities will involve standard NGS techniques. Research & development activities using the same skills are possible. Fundamental understanding of the concepts and methods of PCR, ligation and other enzymatic reactions, strong laboratory skills, organizational skills, note-taking diligence and attention to detail are key. | 1/27/2023 |
| 5356 | Arcturus Therapeutics San Diego, CA Research Associate, Analytical Development Bachelor’s degree in Chemistry, Biochemistry, Molecular Biology, Pharmaceutical, Life Science or equivalent. Exp: Zero to two (0-2) years |
The Research Associate, Analytical Development will be responsible for conducting routine analytical characterization of RNA drug substances, intermediates and formulated drug products to support an emerging research pipeline focused on treating rare diseases. The candidate will also assist with optimization, development and implementation of new analytical procedures as needed. | 1/27/2023 |
| 5357 | Arcturus Therapeutics San Diego, CA Research Associate / Senior Research Associate, Frontier Science Bachelor’s or Master’s Degree in Cellular Biology, Molecular Biology, Biochemistry, or a related field. Exp: 0-3 years |
The Research Associate I/I, Frontier Science will conduct hands-on experiments in the Frontier Science department with a wide variety of cellular biology, molecular biology, and biochemistry techniques. This person will be expected to complete scientific and technical tasks on aggressive timelines and to work as part of a team on varied projects with changing priorities. This position requires excellent communication skills, an outstanding ability to troubleshoot technical issues, a superior ability to plan and carry out experiments independently, and to work with complex instrumentation and software. Exact title and responsibilities will be commensurate with experience. | 1/27/2023 |
| 5358 | Ascendis Pharma Redwood City, CA Research Associate, Analytical Development - CONTRACT Bachelors/Masters degree in chemistry, chemical engineering, biochemistry, or a related field Exp: 0-4 yrs |
The Research Associate will be responsible for conducting laboratory-based analytical development activities to support Ascendis Pharma’s growing pipeline of pre-clinical and clinical programs. Working closely with a team of scientists and engineers in our brand new Redwood Shores laboratory, the Associate Scientist will characterize complex small molecule-based compounds to support process, formulation, and analytical development activities. This position offers great potential for growth of scientific and drug development experience while working on exciting, complex, and impactful products. | 1/27/2023 |
| 5359 | United Therapeutics RTP, NC Research Associate I/II - Analytical Development Bachelor’s degree in arts/sciences (BA/BS) in biology, cell or molecular biology or biomedical sciences Exp: RA I: 1+ years |
Conduct and assist in analytical efforts to evaluate tissue, cell, and cell-secreted products for treating lung disease. | 1/16/2023 |
| 5360 | United Therapeutics Manchester, NH Research Associate I/Research Associate II, Analytical Development, Cell Production Bachelor’s Degree in Arts/Sciences (BA/BS) in cellular biology, developmental biology, biomedical engineering or related field Exp: RA I: 1+ years |
The Research Associate II – Analytical Development will develop and execute analytical methods to support the production of iPS-derived cells and cellularized 3D scaffolds for the development of autologous 3D printed tissue engineered organs. | 1/16/2023 |
| 5361 | United Therapeutics Manchester, NH Associate Process Engineer/ Process Engineer, Biomaterials Bachelor’s Degree in Arts/Sciences (BA/BS) in materials science, chemistry, chemical, mechanical or biomedical engineering (or equivalent) Exp: 1+ years |
The Associate Process Engineer, Biomaterials (OMG) will be responsible for scaling up and experimenting with large batches of ink to support process and product feasibility goals. This position will also be responsible for periodic quality control (QC) testing. | 1/16/2023 |
| 5362 | United Therapeutics RTP, NC Bioprocess Associate I/II - Cell Biology, Bioprocess Development Bachelor’s Degree in Arts/Sciences (BA/BS) in biology, cell and molecular biology, biomedical sciences, biomedical engineering, biomanufacturing, or a Exp: Bioprocess Associate I: 1+ years |
Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. | 1/16/2023 |
| 5363 | United Therapeutics Manchester, NH Research Associate I – Cellularization Bachelor’s Degree in Arts/Sciences (BA/BS) in Cellular Biology, Developmental Biology, or Biomedical Engineering or related field Exp: 1+ years |
The Research Associate I - Cellularization (OMG) will support the development and characterization of bioinks for 3D printing scaffolds for lung tissue engineering. They will design and print 3D diagnostic models to test bionks for compatibility with different lung cell types. | 1/16/2023 |
| 5364 | UPM Pharmaceuticals Bristol, TN Microbiologist 1 Bachelor’s Degree in Microbiology or related science field Exp: 0-2 years |
Learns to and performs routine microbiological quality control testing of pharmaceutical products and related materials in accordance with site policies, departmental procedures, compendial methods and cGMP regulations. Participates in programs to achieve departmental objectives; records and reports results; notes unusual results and notifies supervision for evaluation. | 1/16/2023 |
| 5365 | Upsher-Smith Maple Grove, MN Analyst - QC Bachelor's Degree in Chemistry or related science field Exp: 0 years |
Provides analytical and technical support for analysis of raw materials (drug substances, excipients, in-process samples, and packaging components) stability samples, and drug products. Completes testing in a timely manner according to cGMPs, test methods, and SOPs. Works with dissolution, ion chromatography, pH meters, karl fisher titrations, balances, and various other auxiliary laboratory equipment. | 1/18/2023 |
| 5366 | Vericel Cambridge, MA Technician, Cell Therapy Manufacturing Biotechnology certificate or equivalent Exp: 0-2 years |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. | 1/18/2023 |
| 5367 | Veracyte San Diego, CA Clinical Lab Technician Bachelor’s degree Exp: 1 years |
The Clinical Lab Technician’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. The schedule for this role will be Tuesday - Saturday. | 1/18/2023 |
| 5368 | Verge Genomics South San Francisco, CA In Vitro Senior Research Associate I/II MS in biochemistry, biology or related field Exp: 0-2 years |
Screen compounds in model systems, including successful replication of results in duplicate and triplicate studies Independently plan and perform in-vitro assay and techiques in support of high throughput and medium throughput projects. Directly screen compounds in various in-vitro models including biochemical/ biophysical and mammailan cell culture assays. Review and write SOPs and project research plans | 1/18/2023 |
| 5369 | Vor Biopharma Cambridge, MA Associate Scientist/Senior Associate Scientist, Discovery & Molecular Engineering Bachelor’s or master’s degree in molecular biology, biochemistry, genetics, or a related discipline is required Exp: BS: 0-2+ years’; MS:1+ years |
Vor Bio is seeking an Associate/Senior Associate Scientist, in the Discovery & Molecular Engineering department/team. The candidate will contribute to advancing next-generation editing, including base editing, and characterization approaches towards developing Vor’s genome-engineered hematopoietic stem cell as well as immuno-oncology products. The candidate will work within a team environment to execute experimental plans in cell engineering development within the Discovery & Molecular Engineering team at Vor. | 1/18/2023 |
| 5370 | Voyager Therapeutics Cambridge, MA Research Associate/Sr. Research Associate, Histology For RA, MS Exp: 1+ years |
Reporting to the Senior Scientist, the Research Associate OR Senior Research Associate will contribute to Voyager’s research team at its facility in Cambridge, Massachusetts. This is a hands-on position for a person committed to helping the broader team conduct innovative drug discovery research in a collaborative environment. We are seeking a person who is enthusiastic about biomedical research and can work in close partnership with other scientists and team members. This is an ideal position for an individual with extensive experience in immunohistochemistry (IHC), immunofluorescence (IF), and in-situ hybridization (ISH) assay development. The ideal candidate will demonstrate thorough knowledge of experimental design and independent thinking to support multiple programs. The RA or S. RA must be a highly motivated individual with the ability to oversee project timelines and deliverables and interpret and communicate results. | 1/19/2023 |
| 5371 | ZeptoMetrix North Charleston, SC Chemist, QC I Bachelor's degree in Chemistry or related field. Exp: 1 year |
The Quality Control (QC) Chemist is primarily responsible for the quality control of starting materials, in-process materials and the finished goods. The incumbent must be a dynamic individual who can work in a diversified group and able to handle multi-tasks within QC operations. The candidate must possess a good working knowledge of Analytical Chemistry. This position requires hands on chemistry lab work and troubleshoot instruments and solve complex spectroscopic problems. | 1/19/2023 |
| 5372 | ZeptoMetrix North Charleston, SC Chemist I Bachelor’s degree in Chemistry, Engineering or related field Exp: Up to 2 years |
The Chemist I will involve all manufacturing tasks related to the production of the company’s inorganic products. Responsibilities include manufacturing, handling and packaging of concentrates and single/multi-element reference solutions as per standard operating procedures. The incumbent must be a dynamic individual who can multi-task and perform various activities associated with manufacturing operations while adhering to all safety policies and high quality Standard Operating Procedures. This position requires hands on chemistry lab work and will report to the Inorganic Production Manager. | 1/19/2023 |
| 5373 | Zimmer Biomet Warsaw, IN Technician (718246) College/University courses in Microbiology, Biology, Chemistry, Engineering Mechanics, Medical Technology or other related field preferred. Exp: 0 – 3 years |
Responsible for supporting the daily operations of the laboratory at all Zimmer Biomet Warsaw facilities and for operating and maintaining laboratory equipment for the necessary assigned tasks per area work instructions. May also be responsible for ensuring that equipment calibration and maintenance (preventive and/or corrective) is performed. | 1/19/2023 |
| 5374 | Zimmer Biomet Warsaw, IN Manufacturing Engineer (723066) S. in engineering Exp: 0-3 years |
The manufacturing engineer is responsible for providing manufacturing engineering services to support efficient manufacturing processes. Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. | 1/20/2023 |
| 5375 | Zimmer Biomet Olive Branch, MS Quality Engineer (722350) B.S. in engineering or an alternative Bachelor’s degree program with certification as a quality engineer (e.g. CQE). Exp: 0-3 years |
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. | 1/20/2023 |
| 5376 | Zogenix Cambridge, MA Research Associate I/II - Translational Biology BA/BS or MS Degree in biology, cellular biology, bioengineering or related field Exp: 0-2 years |
We are seeking a Research Associate I/II to join the translational biology group and contribute to translational biology drug discovery efforts. The candidate will be responsible for characterizing and deploying stem cell/3D models and other cellular/biochemical assays to be utilized in early drug discovery for multiple therapeutic programs. He/She will also collaborate in a matrixed team of scientists responsible for identification and knowledge building across pathobiological pathways and patient populations including those in neurology, neuromuscular disease and diseases caused by nucleotide repeat expansions. | 1/20/2023 |
| 5377 | Zogenix Cambridge, MA Senior Research Associate / Biology Protein Sciences BA/BS or MS Degree in biology, biochemistry, chemical biology, protein engineering or related field Exp: RA: 0-2 years |
As a (Senior) Research Associate you will contribute to drug discovery efforts for multiple therapeutic areas including neurology and immunology. You will divide your time between our groups to conduct recombinant protein expression and macrocycle screening for therapeutic programs. This is an exciting opportunity to gain experience in multiple technical areas. | 1/20/2023 |
| 5378 | Accelerate Diagnostics Tucson, AZ Research Associate, Quality Control Bachelor of Science degree in Microbiology, Biochemistry, Molecular Biology, Chemistry, or related life sciences. Exp: 1 year |
The Research Associate for Quality Control is a key member of the Operations Team under the direction of the Team Lead for Consumable Quality Control. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. | 1/20/2023 |
| 5379 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology Exp: 0-3 years |
The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. | 1/20/2023 |
| 5380 | Affinivax Cambridge, MA USP Associate Scientist, Carrier Unit BS/MS in related fields such as Chemical Engineering, Bioengineering, Biochemistry, or Biology Exp: 0-2 years |
Within the Carrier Unit group, you will integrate with a multidisciplinary team in charge of fermentation and purification of recombinant proteins and polysaccharides. You will be in close contact with experts in upstream, downstream and various analytical technologies. Your mission will be focused on the development and execution of upstream processes in different research and development contexts (early development, processability, process development, process understanding, troubleshooting, Life cycle…)The successful candidate will report to the manager of Carrier Unit, which is part of the Microbial Drug Substance organization in Technical R&D (TRD). | 1/20/2023 |
| 5381 | Affinivax Rockville; Boston, MD Associate Scientist Bachelor's degree (biotechnology, molecular biology, biochemistry, molecular, bacteriology, molecular, microbiology). Exp: One or more years |
As Associate Scientist within the Molecular Analytics platform, you will be in charge of implementing, designing and developing methods for the detection and quantification of nucleic acids based on up-todate nucleic acid technologies (NAT) and, in particular, methods aiming at characterizing plasmids (topology, conformation, sequence, quantity, etc.), mRNA Drug Substances (content, integrity, identity) and mRNA-LNP Drug products (monovalent and multivalent), used for production of mRNA vaccines. The use of direct nucleic acid quantification methods (e.g. CRISPR-based assays, digital counting through optical barcodes, branched DNA assays, etc.) will part of the activities of the hired Scientist. | 1/20/2023 |
| 5382 | Affinivax Cambridge, MA Associate Scientist, MAPS Analytical GMP Testing Bachelor/Master of Science in Biology, Molecular Biology, Biochemistry, Chemistry, Analytical Chemistry Exp: 1+ years |
Leveraging our highly innovative Multiple Antigen Presenting System (MAPS) platform technology, we are pioneering the development of a novel class of vaccine. To support this, we have a number of newly created opportunities for Associate Scientists to join our Quality Control Team to support and contribute to our development efforts and ongoing clinical trial. | 1/20/2023 |
| 5383 | Aytu BioScience Grand Prairie, TX Chemist I Bachelor's degree in a science-related field or equivalent experience Exp: 1 year |
The QC Chemist I position plays a key role in the operation of the QC Laboratory. This chemist will be responsible for the timely analysis of a wide variety of samples. The QC Chemist I provide services for other departments (Production, R&D, QA, Engineering), all while operating in a state of compliance with current Good Manufacturing Practices (cGMPs). | 1/20/2023 |
| 5384 | Carmot Therapeutics Berkeley, CA Research Associate I/II, Biology BS or MS in cellular biology, biochemistry, molecular biology or related field Exp: 1-4 years |
As a Research Associate in the Biology group, you will contribute to discovery efforts to identify new drug candidates by generating high-quality screening data using a variety of plate-based cellular and biochemical assays. Additionally, you will help develop new methods to interrogate compound mechanism of action, effect on cell signaling and physiology. This position requires working closely with scientists in biology, pharmacology, and chemistry as part of a multidisciplinary team in a fast-paced environment. At Carmot we value diverse perspectives and encourage our employees to contribute at multiple levels within the company, including strategic development. | 1/20/2023 |
| 5385 | EpiVax Providence, RI Research Associate I Bachelor of Science in Immunology, Biomedical Engineering or Biotechnology is required. Exp: 1-3 years |
The Research Associate I will be responsible for executing scientific research in the laboratory specifically related to the development of vaccines and therapeutic proteins, in addition to maintenance of general laboratory functions. The Research Associate I will be responsible for executing scientific research in the laboratory specifically related to the development of vaccines and therapeutic proteins, in addition to maintenance of general laboratory functions. | 1/20/2023 |
| 5386 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 1/20/2023 |
| 5387 | SparX Therapeutics Mount Prospect, IL Associate Scientist MS degree in biochemistry, molecular biology, or related discipline. Exp: 0-2 years |
SparX is seeking a highly motivated and enthusiastic Associate Scientist in protein expression, purification and characterization. The role will involve cell culture, plasmid preparation, protein expression and purification using a variety of cell culture systems, protein characterization, and evaluation. | 1/20/2023 |
| 5388 | SparX Therapeutics Mount Prospect, IL Associate Scientist Phage Display MS degree in biochemistry, molecular biology, or related discipline. Exp: 0-2 years |
SparX is seeking a highly motivated and enthusiastic Associate Scientist in antibody engineering through high-throughput screening. Experience in phage display is strongly recommended. The role will involve basic molecular cloning, antibody library construction and screening. Knowledge in antibody humanization and affinity maturation is a plus. | 1/20/2023 |
| 5389 | SparX Therapeutics Mount Prospect, IL Research Associate, In Vitro Pharmacology Master’s degree in cell biology, oncology, immunology or related field. Exp: 1+ years |
Position Summary: SparX is looking for a highly motivated, interactive and creative Research Scientist with a strong cell biology background to join the pharmacology team. The primary responsibilities of the Research Associate will be to develop and perform in vitro cellular and/or biochemical assays for antibody drug candidates screening, biological function evaluation in immuno-oncology and oncology drug discovery program. | 1/20/2023 |
| 5390 | SparX Therapeutics Mount Prospect, IL Associate Scientist Cell Culture MS degree in cell biology or related discipline. Exp: 0-2 years |
SparX is seeking a highly motivated and enthusiastic Associate Scientist in Cell Culture. Experience in mammalian cell culture is required. | 1/20/2023 |
| 5391 | Spriaso Salt Lake City, UT Research Chemists Bachelor's degree in chemistry, chemical engineering, biochemistry, or other related degree concentration. Exp: one year |
These positions entails doing product, process, and analytical functions in support of product and technology development under direction of product development and/or analytical leader. | 1/20/2023 |
| 5392 | Aesculap Irvine, CA Microbiologist I Bachelor's degree required. Exp: 0-02 years |
Plans, coordinates and organizes the overall activities of the Microbiological Laboratory according to internal and external standards in a most cost effective way. Directly responsible for the supervision test operation at all time for Sterility Testing, Bacterial Endotoxin Test, Microbiological Identification Sections and handling of laboratory OOS result. Ensures that the necessary microbiological tests are done according to the test specification, test method and working instruction and to ensure release on time for pharmaceutical products and medical devices. | 1/20/2023 |
| 5393 | Aesculap Irvine, CA QC Microbiology Associate II (Micro Product Testing Lab) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. | 1/20/2023 |
| 5394 | Aesculap Irvine, CA QC Microbiology Associate II (Sterility Media) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. | 1/20/2023 |
| 5395 | Aesculap Irvine, CA QC Microbiology Associate II Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. | 1/20/2023 |
| 5396 | Aesculap Irvine, CA Microbiologist (QC Micro Duplex) Bachelor's degree required. Exp: 0-02 years |
The individual will be part of microbiological method validations for the site. This individual will work specifically in Aseptic Fills and Isolators Independently execute existing lab equipment re-qualification and new equipment qualification for the Duplex Facility. Perform variety of routine and non routine tasks including non-conformance and OOS investigation for laboratory and manufacturing operations, writing investigation reports, protocols and updating procedures and other documents. Support other projects assigned as required by the department. | 1/20/2023 |
| 5397 | Aesculap Irvine, CA QC Chemistry Associate II (QC Chem Duplex) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 1/20/2023 |
| 5398 | AGC Biologics Seattle, WA Process Technology Associate - Analytical Bachelor’s Degree or higher in engineering or other science-related field Exp: 0-3+years |
We have an exciting opportunity for a Process Technology Associate to join the Research and Development Center (RD Center) team at AGC Biologics. This is an opportunity to develop next-generation high-throughput analytical techniques through collaboration with the global AGC Biologics RD network. Additionally, this position is responsible for analyzing process samples for cell line development, upstream and downstream development groups within the RD Center. Support activities for the transfer of new technologies into current PD operations may be required. | 1/20/2023 |
| 5399 | Scanogen Baltimore, MD CHEMICAL AND BIOMOLECULAR ENGINEER Chemical Engineering degree Exp: 1+ years |
The main focus is to optimize and automate biomolecule detection assays. | 1/9/2023 |
| 5400 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science Exp: one-year |
Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 1/9/2023 |
| 5401 | SeaGen Bothell, WA Manufacturing Support Associate I Bachelor’s degree preferably in Life Sciences or Engineering. Exp: 0-2 year |
The North Creek Manufacturing Facility at Seagen is seeking a Manufacturing Associate I to participate in cGMP activities in upstream production. The Associate will use their training and knowledge of biopharmaceutical manufacturing to execute operations in a cGMP facility. | 1/9/2023 |
| 5402 | Seran Bioscience Bend, OR Laboratory Technician I Bachelor’s degree or coursework in chemical engineering, chemistry, materials science, or related field preferred. Exp: 0-2 year |
Serán BioScience is looking for a laboratory technician to support and contribute to the development of custom formulations and process development for a variety of pharmaceutical clients. This role requires strong attention to detail and focus within a fast-paced work environment. Successful candidates will demonstrate strengths in teamwork, self-discipline, and proactive communication to ensure collective goals are achieved. Those with limited lab experience are still encouraged to apply. | 1/9/2023 |
| 5403 | Seran Bioscience Bend, OR Scientist/Engineer I, Formulation Sciences B.S. in Science or Engineering discipline. Exp: 0-3 years |
Serán is searching for an entry level scientist or engineer to join our Formulation Sciences team! With mentorship from senior team members, the formulation scientist will investigate the properties of novel pharmaceutical compounds, design formulation strategies to improve drug delivery, and characterize the performance of the enhanced formulations. The ideal candidate has strong communication and collaboration skills to excel in a fast-paced, interdisciplinary team environment. Experience with benchtop laboratory techniques is desired, but scientific curiosity and independent thinking are required for success. | 1/9/2023 |
| 5404 | Seran Bioscience Bend, OR Scientist/Engineer I B.S. or M.S. in Science or Engineering discipline. Exp: 0-3 years |
Serán seeks to hire an entry-level Scientist or Engineer to contribute to pharmaceutical R&D projects in the general area of drug delivery formulation and manufacturing processes. Candidates should possess a bachelor’s or master’s degree in chemistry, chemical engineering, biology, biological engineering, mechanical engineering, materials science and engineering, or physics. Demonstrated research experience is desirable. Candidates with additional relevant experience are also invited to apply. | 1/10/2023 |
| 5405 | Seres Therapeutics Cambridge, MA Research Associate / Senior Research Associate, Microbiology & Functional Screening (100% ON SITE) Bachelors or Masters in Microbiology, Immunology or related scientific field. Exp: BS: +1 year; MS: +0 year |
Seres Therapeutics is seeking experienced and highly-motivated Research Associate to join our Microbiology and Functional Screening team to develop and implement high throughput functional screens that advance the company’s Ecobiotic® therapeutics discovery programs in oncology, infectious and inflammatory diseases. As a member of the Microbiology and Functional Screening team, you will work intimately with research teams across the organization to translate critical insights in the field of the human microbiome into therapeutic leads. The successful candidate will be innovative, thrive in an intense and dynamic environment, and use his/her creative and imaginative problem solving skills to help bring new products to patients. | 1/10/2023 |
| 5406 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field Exp: 6 months |
Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 1/10/2023 |
| 5407 | Smithers Wareham, MA Associate Chemist I - Chemistry Bachelors or better in Chemistry or related field. Exp: 6 months |
Position is expected to perform varied and often complex and difficult procedures somewhat independently. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Operates and may maintain, under supervision, test equipment and apparatus of moderate complexity. May provide information for initial data interpretation and test system conformance to expectations. Records, compiles and reduces laboratory data in real time in a complete and thorough manner for individual assignments. May produce reports. | 1/10/2023 |
| 5408 | Smithers Wareham, MA Assistant Biologist - Ecotoxicology Bachelors or better in Biology or related field. Exp: 6 months |
Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. Incumbent will be introduced to mathematical and statistical procedures used to reduce and analyze study data. Responsible for maintaining cleanliness of the labs, storage and culture areas including maintenance and calibration of equipment used in any of these settings. May require routine involvement in seawater and/or sediment collection. Assignments are completed with minimal supervision. Assists with organization, direction and training of technicians. Assists in coordinating internal requirements for testing (i.e. chemistry support, Quality Assurance, reporting). Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations and company policies. | 1/10/2023 |
| 5409 | Smithers Wareham, MA Smithers Cannabis Testing Services Division, MA - Associate Chemist I BS. degree in chemistry or related field. Exp: 6 months |
Essential Functions: Cannabis sample processing of flower, concentrates, extracts, and infused products. Cannabis sample extraction & dilutions. Routine maintenance of laboratory equipment and instrument calibration. Wash glassware used by the laboratory. Accurate entry of sample data into LIMS. Production of laboratory reagents and stocks. | 1/10/2023 |
| 5410 | Smith and Nephew Fort Worth, TX QC Microbiologist 1 Bachelor of Science in Microbiology or related scientific discipline required Exp: 1 - 3 years |
This position will perform in a GMP environment following FDA and ICH guidelines. Duties include product release testing per USP Microbial Limits testing, product stability testing, environmental sampling of controlled ISO 5-8 classified areas and controlled unclassified areas, preparation of media and cultures, growth promotion, purified water sampling, preparation and sterilization of equipment. | 1/10/2023 |
| 5411 | Smith and Nephew Fort Worth, TX QC Microbiologist 1 Bachelor of Science in Microbiology or related scientific discipline required Exp: 1 - 3 years |
This position will perform in a GMP environment following FDA and ICH guidelines. Duties include product release testing per USP Microbial Limits testing, product stability testing, environmental sampling of controlled ISO 5-8 classified areas and controlled unclassified areas, preparation of media and cultures, growth promotion, purified water sampling, preparation and sterilization of equipment. | 1/10/2023 |
| 5412 | Smiths Medical Austin, TX Chemistry Analyst I - Nights - (22301793) Bachelor’s Degree is required: Chemistry, Chemical Engineering, or Chemical Science Exp: 0-2 year |
The Chemistry Analyst I will work under direct supervision or be partnered with an experienced analyst to perform wet chemistry analyses, preparation of reagents, standardization of solutions, and instrumentation testing and documentation in a cGMP environment. May be cross-trained to work in other laboratory areas as dictated by the needs of the department. | 1/10/2023 |
| 5413 | Sofregen Medical Framingham, MA Quality Engineer Bachelor’s degree in scientific discipline. Exp: 0-2 years |
Sofregen Medical is seeking a Quality Engineer to join our Manufacturing team and support the production of Sofregen’s commercial silk-based medical device platform. The Quality Engineer plays a vital role in the maintenance of the Quality Management System as well as the daily operation of the laboratory. Duties will include maintaining a system to track equipment calibration & maintenance, environmental monitoring, inventory management, receiving and incoming inspection, and authoring routine Quality Control documentation (e.g. deviations, standard operating procedures (SOPs), batch records, etc.). The Quality Engineer will further collaborate with Manufacturing members to provide general support to critical processes. | 1/10/2023 |
| 5414 | Sonosite Mesa, AZ PROCESS ENGINEER - CMP BS in Chemical Engineering Exp: Zero to two years |
The CMP Process Engineer provides engineering and technical support to the CMP Manufacturing team to assure that all products manufactured meet the quality and cost requirements of the CMP business, and the quality, volume, and availability requirements of our customers. The CMP Process Engineer also assures that all ongoing operations and any proposed expansion of operations fully meet the EH&S targets and objectives for the Mesa site. | 1/10/2023 |
| 5415 | Spotlight Therapeutics Hayward, CA Research Associate (RA) - Protein Engineering BS/MS in Biochemistry, Molecular Biology, Genetics, or related field Exp: 1-2 years |
Primary responsibilities will include several aspects of protein engineering, such as plasmid construct design, protein expression, and purification. In addition, biochemical assays would be carried out to assess purity, concentration, stability, integrity, and enzymatic activity of RNPs. This position requires a minimum of 1-2 years of laboratory experience, with demonstrated expertise in biochemistry and molecular biology. Ideally, the candidate will have experience with molecular cloning, the production of recombinant proteins, and the design and execution of biochemical assays. | 1/10/2023 |
| 5416 | Spotlight Therapeutics Hayward, CA Research Associate (RA) - Monogenic Diseases BS/MS in molecular biology, cellular biology, or related field Exp: 1-2 years |
We are looking for an enthusiastic research associate to join our biology team. This candidate will help develop various primary cell models, be responsible for testing engineered RNPs, and evaluate downstream editing. The candidate will also help in identifying disease targets and will screen guides for different disease indications. This individual will work across different teams to advance numerous projects. The candidate will have opportunities for professional growth and development in a fast-growing biotechnology start-up. | 1/10/2023 |
| 5417 | Stability Biologics San Antonio, TX QA Specialist - San Antonio, TX BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.) Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 1/10/2023 |
| 5418 | Stellartech Research Milpitas, CA Quality Engineer II BS degree or equivalent. Exp: 1-3 years |
Stellartech is looking for a Quality Engineer to join our Team. | 1/11/2023 |
| 5419 | Strand Therapeutics Boston, MA Associate Scientist, LNP Discovery B.S. or M.S. in Pharmaceutical Sciences, Biomedical Engineering, Chemical Engineering or other relevant scientific disciple. Exp: 1-3+ years |
We are looking for a highly motivated and innovative candidate for the role of Associate Scientist, LNP Discovery. The expectation is that the candidate will have experience in the formulation and characterization of LNPs. The candidate will be expected to work in an innovative, fast-paced, cross-collaborative biotech environment and contribute in multi-disciplinary team activities to advance our platform. This role will have the opportunity to collaborate with functions outside of LNP Discovery such as Translational biology, LNP Process Development, and Analytical Development. | 1/11/2023 |
| 5420 | Strand Therapeutics Boston, MA Associate Scientist/Sr Associate Scientist, RNA Discovery Biology M.S. Exp: 1 year |
We are looking for an Associate Scientist/Sr Associate Scientist to support our molecular and cell biology needs to enable the drug discovery efforts within the RNA Discovery Biology team at Strand Therapeutics. The ideal candidate will have experience in mammalian cell culture including primary cell isolation and handling. The candidate will be expected to work in an innovative, fast-paced, cross-collaborative biotech environment and contribute in multi-disciplinary team activities to advance our platform. | 1/11/2023 |
| 5421 | Strand Therapeutics Boston, MA Associate Scientist, In Vivo Pharmacology B.S. or M.S. in Biological Sciences, Bioengineering or related discipline. Exp: 1-3+ years |
We are looking for an Associate Scientist to join the In Vivo Pharmacology group to conduct proof-of-concept, validation, and pharmacology studies to support multiple pre-clinical programs. You will be passionate about scientific discovery, undeterred by bold challenges, and enjoy working as a team to develop the next generation of mRNA medicines. You should be highly organized, a critical thinker, adaptable to changing priorities, and possess a strong ability to collaborate effectively with teams of diverse backgrounds. | 1/11/2023 |
| 5422 | Surgalign San Diego, CA Quality Engineer Bachelor’s Degree in Engineering, or related field required Exp: 1-3 years |
The Quality Engineer works on a cross-functional team including Research & Development, Marketing, Regulatory, Supply Chain, and others to support new product development, specifically with review of design control documentation such as design and development plans, inputs, outputs, and verification and validation activities. Additional activities include drafting project quality plans, standard operating procedures, risk management, and test protocols/reports. | 1/11/2023 |
| 5423 | Taconic Biosciences Rensselaer, NY Senior Laboratory Specialist Molecular Analysis Bachelor’s Degree from a four-year college or university. Exp: 1 year |
The Senior Laboratory Specialist performs a variety of molecular assays on animal samples and must be able to generate high-quality results in a timely manner. This individual should be comfortable working in a high-throughput environment and be able to use proper judgement to make technical decisions on assay performance issues. | 1/11/2023 |
| 5424 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, Cell Therapy Discovery BS/MS degree in biological sciences Exp: 1+ years |
We are looking for a Research Associate to join the Cell Therapy Discovery team to advance early-stage cell-based research with Tessera’s novel Gene Writing and Gene Rewriting technology for ex vivo and in vivo cell therapy applications. The Senior Research Associate will work closely with scientists in the Cell Therapy team to translate novel gene writing technologies to develop innovative therapeutics for Oncology disorders. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 1/11/2023 |
| 5425 | Tessera Therapeutics Somerville, MA Research Associate I/II, High Throughput Synthesis BS/MS degree. Exp: 0-3+ years |
The Research Associate I/II will be responsible in designing, synthesizing and purifying oligonucleotides for research studies and high throughput format. We are searching for a driven, enthusiastic, and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 1/11/2023 |
| 5426 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, Stem Cell Biology BS/MS degree in biological sciences Exp: 1+ years |
We are looking for a Research Associate to join the In Vivo Rewriting Candidate Development team to advance translational research with Tessera’s novel Gene Writing and Gene Rewriting technology for in vivo gene therapy applications. The Research Associate will work closely with scientists to translate novel gene writing technologies to develop innovative therapeutics. We are searching for a driven, enthusiastic, and self-motivated individual who is comfortable multi-tasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 1/11/2023 |
| 5427 | Tri-Pac South Bend, IN Associate Engineer Bachelor’s degree in Engineering or equivalent. Exp: 0-2 years |
The Associate Engineer is a team player who can work independently or in a team setting with minimal supervision. He/she must possess good communication skills which will be used to contribute to ongoing initiatives, is detail oriented and task driven towards learning various systems and device functions. The Associate Engineer is actively involved with validation and quality activities required to support the Production Department. | 1/11/2023 |
| 5428 | Tris Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field. Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. | 1/11/2023 |
| 5429 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate, In Vivo Pharmacology (RA07-7) For RA level: BS; For Sr. RA level:MS Exp: RA: 0-3+ years ; Sr. RA: 0-2+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a motivated researcher to join our In Vivo Pharmacology team as a Research Associate/Senior Research Associate, supporting the preclinical development of our lead therapeutic TCRs. The ideal candidate should have relevant experience in in vivo pharmacology, mechanism of action and anti-tumor efficacy studies, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 1/12/2023 |
| 5430 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate, TCR Discovery (RA05-9) B.S. or M.S. Exp: B.S: 0-5 years; MS: 0-2 years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for an experienced researcher to join our team as Research Associate or Senior Research Associate, supporting our novel TCR discovery workflow in house. The ideal candidate should have relevant experience in T cell immunology, cancer cell culture and flow cytometry, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a willingness to learn will thrive in this role. | 1/12/2023 |
| 5431 | Turn Biotechnologies Mountain View, CA Research Associate / Sr. Research Associate - Biology BS/MS in biology, biochemistry, molecular biology, or related discipline. Exp: one year |
Turn Biotechnologies is currently seeking a qualified, highly motivated individual for the position of Sr. Research Associate – Biology. This person will be a highly motivated and responsible individual whose primary purpose is to perform and assist with experiments, analyze data, maintain records, manage projects, maintain lab operations, and other duties as required to meet company goals. | 1/12/2023 |
| 5432 | Twist Bioscience South San Francisco, CA Research Associate B.S. or M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field Exp: 0-2 years |
In this position, you will have the opportunity to work on leading-edge products for genomics, diagnostics, and personalized medicine. First and foremost, we are looking for someone with a scientist’s mindset. Creativity, critical thinking, careful experimental execution, and a desire to learn deep technical details are a must. This position is geared towards working with the DNA and RNA product lines. The candidate must be capable of maintaining current products, troubleshooting control fragment assembly issues, and analyzing data related to current and future controls. Up-and-coming scientists that demonstrate self-motivation and enthusiasm for scientific bench work are strongly encouraged. Your work will be mainly at the bench; however, you will have the opportunity to use high-throughput robotic instruments as well as coding and bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 1/12/2023 |
| 5433 | Twist Bioscience South San Francisco, CA Research Associate, Antibody Engineering BS Exp: 1-year |
We are seeking an outstanding, innovative, and creative Research associate to join our antibody discovery effort. This research associate will play multiple roles within the Biopharma group and will work within a team responsible for antibody discovery utilizing a number of in vitro display technologies, e.g. phage display, ribosome display, and yeast display. | 1/12/2023 |
| 5434 | Twist Bioscience South San Francisco, CA Research Associate, Flow Cytometry Bachelor’s degree in Biology, Biotechnology, or a related scientific discipline Exp: 0-3 years |
We are seeking a motivated individual to join our expanding flow cytometry team. Using state-of-the-art technology, the candidate would help accelerate our antibody discovery process through careful cell culture maintenance and flow cytometry screening. Highly qualified candidates will have experience with a variety of mammalian-based cell culture methods and techniques. Prior flow cytometry experience is desired. | 1/12/2023 |
| 5435 | Twist Bioscience South San Francisco, CA Research Associate, NGS Bachelors/ Associates degree in biology, chemistry, biochemistry Exp: 1-3 years |
Twist is seeking a highly motivated individual to help support customers and their Next Generation Sequencing needs. This individual will work closely with R&D and Customer Support teams to help develop custom solutions for various sequencing applications. The candidate will be detail oriented who is compatible with fast paced environments. | 1/12/2023 |
| 5436 | Twist Bioscience South San Francisco, CA Research Associate, NGS Viral Controls B.S. or M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field. Exp: 0-2 years |
This position is geared towards working with the DNA and RNA controls product lines. The candidate must be capable of maintaining current products, troubleshooting control fragment assembly issues, and analyzing data related to current and future controls. Up-and-coming scientists that demonstrate self-motivation and enthusiasm for scientific bench work are strongly encouraged. Your work will be mainly at the bench; however, you will have the opportunity to use high-throughput robotic instruments as well as coding and bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 1/12/2023 |
| 5437 | Twist Bioscience South San Francisco, CA Research Associate, Process Development B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
We are looking for an outstanding Research Associate to join our Specialty Production Team in South San Francisco. The Research Associate will support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast-paced startup environment. The ideal candidate will work independently, be very organized, have excellent molecular biology knowledge and skills, and communicate effectively with peers/management. The Candidate must be comfortable working in a LEAN manufacturing/ controlled laboratory environment. | 1/12/2023 |
| 5438 | Ultragenyx Pharmaceutical Cambridge, MA Senior Research Associate, Vector Core - Gene Therapy MSc in Biology, Molecular Biology, Biochemistry, Virology or cognate discipline. Exp: 1-3 years |
Reporting to the Senior Director of Vector Platform Research, the Senior Research Associate will support and execute the production and purification of rAAV from HEK and HeLa Producer Cell Line systems, as well as iterative improvement of these processes by performing hypothesis-driven research. This role will place specific emphasis on the downstream purification of rAAV including chromatography (primarily with AKTA FPLC systems), filtration processes, and final formulation of research grade material. | 1/12/2023 |
| 5439 | Proteintech Rosemont, IL Scientist I, Bioconjugation Bachelor’s degree in an appropriate area of specialization (Molecular Biology, Cell Biology, Biochemistry, or related life sciences). Exp: New grads |
New grads with lab experience are encouraged to apply. The successful candidate will support the development and optimization of processes in bioconjugation of antibodies for use in various applications like Flow Cytometry and IHC. | 1/2/2023 |
| 5440 | Pyxant Labs Salt Lake City, UT QC Reviewer II Bachelor of Science/Arts (BS/BA) degree. Exp: One year |
Reviews data for accuracy and compliance to applicable Standard Operating Procedures (SOPs) and regulations. Maintains and expands knowledge of regulatory requirements, SOP requirements, and client requirements. Performs follow up actions to reduce departmental citations from QA as needed. Maintains error tracking data in support of departmental improvement efforts. | 1/2/2023 |
| 5441 | Quanterix Billerica, MA Manufacturing Associate I, Downstream BS in Chemistry, Biology or related Life Sciences Exp: 0+ years |
We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 1/2/2023 |
| 5442 | Quanterix Billerica, MA Manufacturing Associate I Upstream BS in Chemistry, Biology or related Life Sciences required. Exp: 1+ years |
We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 1/2/2023 |
| 5443 | Quidel San Diego, CA Bioengineer Master’s degree in biochemistry, chemistry, physics, bioengineering, related field, or equivalent. Exp: 1 year |
Quidel is looking for a Bioengineer to join our team in the Mira Mesa area of San Diego. The Bioengineer provides technical expertise to the design and development of new and novel medical device product(s). Designs and implements new methodologies, materials, machines, processes, or products. Develops new concepts from initial design to market release. Conducts feasibility, development, verification and validation studies of the design to determine the product’s ability to function as intended. Maintains detailed documentation throughout all phases of research and development. Coordinates activities with outside suppliers and consultants to ensure the delivery of supplies or services needed to meet scheduled timelines. | 1/2/2023 |
| 5444 | Quidel San Diego, CA Development Associate II (Assay Development) MA/MS in life sciences. Exp: 0-2 years’ |
Responsibilities include activities to support research and new product development. Perform self-directed experiments or as directed by Scientist or Manager. | 1/3/2023 |
| 5445 | Quotient Sciences Garnet Valley, PA Associate Formulator B.S. Degree in Chemical Engineering, Pharmacy/Pharmaceutical Sciences or other related field. Exp: 0-2 years’ |
To conduct formulation development and manufacturing related activities. To comply & adhere to Good Manufacturing Practice (GMP) standards. | 1/3/2023 |
| 5446 | QuVA Pharma Bloomsbury, NJ Sterility Assurance Specialist 2nd shift Bachelors or better in Microbiology or related field. Exp: 1-2 years |
Schedule & Proctor Media Fills Performs reading of media aseptic process simulations and Environmental/Personnel Monitoring (EM/PM) plates and accounting of all units Performs EM/PM sampling Maintains EM/PM records Periodically reviews Environmental/Personnel monitoring data to identify any potential trends Providing training support for personnel on appropriate aseptic techniques and gowning techniques including execution of Compounder Competency Assessments | 1/3/2023 |
| 5447 | QuVA Pharma Bloomsbury, NJ Sterility Assurance Specialist 1st shift Bachelors or better in Microbiology or related field. Exp: 1-2 years |
Schedule & Proctor Media Fills Performs reading of media aseptic process simulations and Environmental/Personnel Monitoring (EM/PM) plates and accounting of all units Performs EM/PM sampling Maintains EM/PM records Periodically reviews Environmental/Personnel monitoring data to identify any potential trends Providing training support for personnel on appropriate aseptic techniques and gowning techniques including execution of Compounder Competency Assessments | 1/3/2023 |
| 5448 | QuVA Pharma Bloomsbury, NJ Chemist 1st shift B.S. or M.S. degree in chemistry, biology or related field. Exp: 0- 2 years |
Reads and understands SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements Provide analytical data in a timely manner. This includes understanding of Supervisor or Manager’s expectations Provide input to R&D SOPs to enhance the efficiency of the laboratory Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements Communicate as needed any testing issues to either a Supervisor or Manager or to a cross-functional group such as Metrology | 1/3/2023 |
| 5449 | QuVA Pharma Bloomsbury, NJ Chemist 2nd shift B.S. or M.S. degree in chemistry, biology or related field. Exp: 0- 2 years |
Reads and understands SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements Provide analytical data in a timely manner. This includes understanding of Supervisor or Manager’s expectations Provide input to R&D SOPs to enhance the efficiency of the laboratory Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements Communicate as needed any testing issues to either a Supervisor or Manager or to a cross-functional group such as Metrology | 1/3/2023 |
| 5450 | Rani Therapeutics San Jose, CA MECHANICAL ENGINEER Bachelor’s Degree in Mechanical Engineering Exp: 1-3 years |
We are seeking an exceptional Mechanical Engineer to design and develop semi or fully automated equipment that are used for high volume, disposable devices. Your role is to find creative and sound engineering solutions to challenging problems with strong focus on quality, reliability and execution. This is a hands-on position that requires interaction and collaboration with a cross-functional team including Engineering, Manufacturing, Biology, Quality, Facilities and Sustaining. | 1/3/2023 |
| 5451 | Rapid Micro Biosystems Lowell, MA Research Associate I Bachelor’s degree in Microbiology, or Biological sciences. Exp: 0-2 years’ |
We are seeking Research Associate I for the R&D Microbiology group based in Lowell, MA emphasizing teamwork, creativity, and intellectual achievement. The candidate will have the opportunity to work closely with our highly skilled scientists and engineers on a variety of cross-functional projects in developing new applications, technologies, and products for rapid microbial enumeration assays. You should be an energetic self-starter with documented productivity and integrity; strong organizational, interpersonal, and communication skills required. | 1/3/2023 |
| 5452 | Reaction Biology Malvern, PA Research Associate I – Biochemical Assays Bachelor’s Degree or equivalent in biochemistry or related discipline Exp: 0-3 years |
Reaction Biology (RB) is a private pharmaceutical research company. We provide contract research services to over 1500 clients worldwide through our labs in Malvern, PA and Freiburg, Germany. We are currently seeking a Research Associate I for our Malvern, PA facility. We are looking for a reliable and motivated individual with a strong science background to work in our lab. The position is a bench position with the primary duty of executing a variety of enzymatic assays. | 1/4/2023 |
| 5453 | Reata Pharmaceuticals Irving, TX Research Associate, Molecular and Cell Biology BSc in biological sciences Exp: 1 - 3 years |
We are looking for a Research Associate with basic knowledge of cell biology and biochemistry to join our dynamic team of researchers. With guidance, the successful candidate will be expected to execute routine experiments in support of our drug discovery and development programs. Demonstrated technical proficiency and capacity for problem-solving are a plus. Ability to work in a fast-paced environment with rapidly changing priorities is desired. | 1/4/2023 |
| 5454 | Replimmune Framingham, MA Validation Associate Bachelor’s degree in science, Technology, Engineering, and/or Math (STEM) field is preferred. Exp: one-year |
The Validation Associate is responsible for the maintenance and execution of validation protocols for qualification and requalification of equipment at the Framingham, MA, manufacturing facility in accordance with appropriate regulatory guidance. The individual will work with equipment vendors and external contractors to coordinate scheduling, execution and review of qualification protocols / reports. The Validation Associate’s primary responsibility is to perform field executions for various protocols necessary for GMP equipment and systems. The individual will contribute to maintaining the validated status of the facility and equipment through calibration, performance monitoring, data integrity assessments, and requalification activities. | 1/4/2023 |
| 5455 | R & D Systems Austin, TX Research Associate Bachelor’s degree in biology, chemistry, biomedical engineering, or related field is required. Exp: 1-3 years |
Asuragen is seeking an outstanding BSc-level scientist to join our Research group. This is a full time position focused on developing innovative nucleic acid or protein-based technologies. This role will support new product initiatives to enable novel, multiplexed-PCR technologies that can resolve multiple classes of DNA/RNA markers or proteomics through integration of reagents, instrumentation, analysis algorithms and software. Platforms used in our laboratory include quantitative real-time PCR, digital PCR, capillary electrophoresis, next-generation and long-range sequencing. | 1/5/2023 |
| 5456 | R & D Systems Minneapolis, MN Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Tuesday through Saturday workweek. | 1/5/2023 |
| 5457 | R & D Systems Minneapolis, MN Quality Technician MLT/MLS degree, Bachelor’s degree in Biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. You will assist the QC Laboratory Manager/Supervisor with releasing products to bottle and ship, proofing labels and assay sheets. You will serve as a member of the Technical Service team by rotating through our Technical Service Department and responding to customer inquiries and complaints with the assistance of senior members of the department. This position will adhere to safety regulations. Perform additional duties as assigned. | 1/5/2023 |
| 5458 | R & D Systems San Marcos, CA Research Associate - Advanced Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field preferred. Exp: 1-5 years |
Responsible for developing controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for developing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to research in a laboratory environment. | 1/5/2023 |
| 5459 | Roche Carlsbad, CA Research Associate II Assay Development M.S. in Bioengineering, Biochemistry, Molecular Biology, Analytical Chemistry or a related field. Exp: 0+ years |
The Research Associate II will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision. You will investigate, adapt or modify experimental methods and technologies for project advancement. This is a unique opportunity to leverage your background and skills in molecular diagnostics to enhance and build your career by working cross-functionally. An exciting career opportunity where your contributions will impact business opportunities through successful completion of projects. | 1/5/2023 |
| 5460 | Roivant Sciences Boston, MA Research Associate, Automation and Assay Operations (Covant Therapeutics) Sc. or M.Sc. degree in biology, biochemistry, organic, analytical chemistry or related discipline. Exp: 1+ years |
The successful candidate will have a background in laboratory automation techniques and ideally have a track record of accomplishments in academia or in the life sciences/pharmaceutical/biotechnology industry. Our group is committed to the professional and scientific growth of our team members. As a result, s/he must have a strong desire to learn. The successful candidate will have the opportunity to acquire novel analytical and scientific skills and will be exposed to cross-functional and collaborative drug discovery in a biotechnology environment. | 1/5/2023 |
| 5461 | SAMDI Tech Chicago, IL Research Assistant B.S. in biology, biochemistry, chemistry, or related field. Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. | 1/5/2023 |
| 5462 | Sanofi Pasteur Waltham, MA BioProcess Analytics Research Associate BS in biological sciences or related field. Exp: 0 – 2 years |
The BioProcess Analytics support group located in Waltham, MA is responsible for execution of analytical methods to support manufacturing and development activities, building process understanding, and supporting life cycle management from early to late stage clinical entry. The Research Associate (Analytical Technician) is responsible for executing test methods under control of established procedures. We are looking for a candidate that has experience in an analytical setting that can independently manage and execute their testing schedule supportive of genomic medicines process development. In addition, they should possess the skills to interpret and communicate their data with the appropriate development teams. | 1/5/2023 |
| 5463 | Sanofi Pasteur Waltham, MA mRNA, Research Associate, Gene Synthesis - Vaccine M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology). Exp: 1-3 years |
As an experienced Plasmid DNA Research Associate, you will be responsible for supporting the efforts to establish a high throughput gene synthesis workflow initiating with design and ending in analytical methodologies. | 1/5/2023 |
| 5464 | Sanofi Pasteur Framingham, MA Senior Research Associate Master's degree in Biochemistry, Pharmaceutical Sciences, Chemical Engineering, Biological Engineering. Exp: 0+ years |
We are seeking a highly motivated and talented Senior Research Associate (SRA) to join our Formulation and Process Development (FPD) group. FPD is part of the global Biologics Drug Product Development & Manufacturing group, a critical R&D function enabling the manufacturing of stable and deliverable dosage forms along the complete development timeline from molecule selection to commercial tech transfer. The selected candidate will be responsible primarily for formulation and process development for protein and monoclonal antibody therapeutics for liquid and lyophilized dosages. Key expectations and training will include solid understanding in protein structure, chemistry, and characterizations. You will be part of a team with global responsibility for formulation and process development for Protein therapeutics and Gene Therapy. The candidate will have the opportunity to work on different facets of drug product formulation and process development for different modalities such as monoclonal antibodies (mAb), multi-specific antibodies, therapeutic enzymes, fusion proteins, viral capsids (recombinant AAV and Lentiviral vectors), Lipid Nanoparticles and Cell Therapies | 1/5/2023 |
| 5465 | Sanofi Pasteur Framingham, MA Research Associate Cell Culture Development Bachelor's degree in Chemical Engineering, Biochemical Engineering, Biochemistry or related discipline. Exp: 0+ years |
We are looking for candidates for a position at the level of Research Engineer. This individual will join a dynamic and motivated team to develop cell culture processes in support of early and late stage drug development programs, as well as tech transfer of the developed process into the clinical manufacturing team or Industrial Affairs organization. She/he will evaluate new technologies and develop platform technologies suitable for incorporation into our upstream process. He/she will ensure that the highest standards of safety and environmental compliance are maintained in the workplace and operate under the regulatory requirements for biologics product development and manufacturing. | 1/5/2023 |
| 5466 | Sanofi Pasteur Cambridge, MA Research Associate - Biomarkers and Clinical Bioanalyses Bachelor’s degree or Master’s degree in the field of immunology, biochemistry, biology, or other life-science field. Exp: BS: 1-3 years’; MS: 0-2 years |
We are seeking a Research Associate to join the Bioanalysis group within Biomarkers & Clinical Bioanalysis (BCB), a global department within the Translational Medicine and Early Development unit of Sanofi. This position will work in a team setting to develop and validate assays, as well as support sample analysis in a regulated environment. The primary laboratory responsibilities of this position require the candidate to be on-site 5 days a week. | 1/5/2023 |
| 5467 | Sanofi Pasteur Framingham, MA Senior Research Associate Purification Process Development Master's degree in Chemical Engineering, Biochemical Engineering, biochemistry or related discipline. Exp: 0+ years |
We are looking for candidates for the position of Senior Research Associate. This individual will join a dynamic and motivated team to develop downstream purification processes in support of early and late-stage drug development programs. In addition, the Senior Research Associate will support the tech transfer of the developed process into the clinical manufacturing team or Industrial Affairs organization, while ensuring the highest standards of safety, environmental, and regulatory compliance are maintained in the workplace. | 1/5/2023 |
| 5468 | Sanofi Genzyme Waltham, MA Senior Research Associate Drug Product Master’s degree in biochemistry, pharmaceutical science, chemical engineering, or a related discipline. Exp: 0+ years |
The Senior Research Associate will be a part of the Global Drug Product Development & Manufacturing group. The candidate will primarily support Biopharmaceutical Drug Product development projects for Gene Therapy (in support of the Genomic Medicine Unit) and Protein therapeutic programs. The candidate will have the opportunity to work on different facets of drug product development for different modalities such as Lipid Nanoparticles, gene therapy capsids (recombinant AAV capsids), Cell Therapy and Protein/Enzyme therapeutics | 1/5/2023 |
| 5469 | Sanofi Genzyme Swiftwater, PA Senior Production Technician - Vaccines Bachelors Exp: 1 + years |
This role is for a non-exempt employee working in the Filling Department. Their Bi-weekly pay is based on previous experience and education time. | 1/5/2023 |
| 5470 | Sanofi Genzyme Swiftwater, PA Fill LL-2 - Vaccines Associate or Bachelors' degree in Life Sciences or other relevant fields of study. Exp: no experience |
The production technician is the “heartbeat” of the vaccine manufacturing and is primarily responsible for the high quality and efficient production of our vaccines in accordance with current good manufacturing practices (cGMP) for all relevant regulatory agencies (e.g., FDA). | 1/5/2023 |
| 5471 | Sanofi Genzyme Waltham, MA mRNA, Research Associate, Gene Synthesis - Vaccine M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology). Exp: 1-3 years |
As an experienced Plasmid DNA Research Associate, you will be responsible for supporting the efforts to establish a high throughput gene synthesis workflow initiating with design and ending in analytical methodologies. | 1/5/2023 |
| 5472 | Sanofi Genzyme Waltham, MA mRNA - Senior Research Associate, Plasmid Production M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology). Exp: 1-3 years |
As an experienced molecular biologist, you will be supporting thedesign, development and implementation of a robust plasmid growth, extraction, and purification process for preclinical supercoiled and linearized plasmid production. | 1/5/2023 |
| 5473 | Sanofi Genzyme Waltham, MA Senior Research Associate Purification Process Development Master’s degree in chemical or biochemical engineering or related disciplines. Exp: 0+ years |
We are looking for a candidate with experience in AAV purification development, scale-up, and pilot manufacturing, and technology transfer. | 1/5/2023 |
| 5474 | Sarepta Therapeutics Durham, NC Contract Research Associate I B.S. degree in Molecular Biology, Biochemistry, Immunology, Cell Biology, Bioengineering, or related field. Exp: 1 year |
The Research Associate I provides laboratory support, performs experiments, and collects data on in vitro, ex vivo, and/or in vivo studies to investigate the effects of CRISPR-based gene editing on gene and protein expression, tissue pathology, and disease phenotype in animal models of neuromuscular and/or neurodegenerative disorders. This role provides laboratory support of day-to-day GCLP analyses and develops cutting-edge CRISPR-based technology platforms for research and therapeutic applications. | 1/5/2023 |
| 5475 | Sarepta Therapeutics Andover, MA QC Associate I BS in Chemistry or related science field. Exp: 0-2 years’ |
This individual will support quality control activities conducted both internally and at the Contract Test Laboratories (CTLs). The individual will be responsible for reviewing release and stability data, writing technical reports, supporting analytical method validation and qualification activities conducted at the CTLs. This individual will assist in transferring assays to and from domestic and overseas vendors and monitoring, compiling and reviewing data. The individual will also assist in managing quality events, data trending, review of quality documents originated at the testing laboratories as well as internally at Sarepta. All aspects of this position would involve working in a GMP compliant manner. | 1/5/2023 |
| 5476 | Sarepta Therapeutics Andover, MA Contract Laboratory Operations Assistant B.S degree in Biology, Chemistry, or related field. Exp: 2 years |
The Research Operations team at Sarepta Therapeutics is seeking a motivated laboratory operations associate to assist with routine laboratory operations and help implement compliance in a clinical laboratory setting. This includes day-to-day laboratory operations, sample and equipment management, and implementing new processes within the lab for laboratory compliance. | 1/5/2023 |
| 5477 | Sarepta Therapeutics Durham, NC Contract Research Associate I B.S. degree in Molecular Biology, Biochemistry, Immunology, Cell Biology, Bioengineering, or related field. Exp: 1 year |
The Research Associate I provides laboratory support, performs experiments, and collects data on in vitro, ex vivo, and/or in vivo studies to investigate the effects of CRISPR-based gene editing on gene and protein expression, tissue pathology, and disease phenotype in animal models of neuromuscular and/or neurodegenerative disorders. This role provides laboratory support of day-to-day GCLP analyses and develops cutting-edge CRISPR-based technology platforms for research and therapeutic applications. | 1/5/2023 |
| 5478 | Sarepta Therapeutics Andover, MA Contract Lab Operations Assistant Associate or B.S degree in Biology, Chemistry, or related field. Exp: 1 year |
This individual will support laboratory operations at Sarepta Andover, MA site. This individual will support the day-to-day laboratory operations including but not limited to reagent ordering, receiving and inventory, and sample and equipment management. All aspects of this position involve working in a GMP-compliant manner. | 1/5/2023 |
| 5479 | Olaris Therapeutics Framingham, MA RESEARCH ASSOCIATE B.S. or MS Degree in Biology, Biochemistry, Chemistry, or related field Exp: 1 - 3+ years |
The successful candidate will be responsible for a broad range of activities including metabolite extraction from patient biofluids, NMR and MS sample preparation and analysis, sample organization and handling. You will be responsible for maintaining a proper lab notebook. You will be expected to maintain a clean lab space and follow all safety guidelines. This position includes the opportunity to learn advanced NMR and MS techniques. | 12/26/2022 |
| 5480 | Ology Bioservices East Norriton, PA Research Associate I, Cell Therapy Process Development Bachelor’s or Master’s degree in immunology, cell biology, bioengineering or a related field. Exp: 0 - 2 years |
Resilience is seeking a talented Research Associate I to expand our cell therapy process development team. With the guidance of process development senior staff, this researcher will develop and optimize manufacturing processes for gene-modified cell products to advance Resilience’s biomanufacturing platforms and the clinical programs of Resilience’s partners. | 12/26/2022 |
| 5481 | Ology Bioservices East Norriton, PA Bioprocess Technician I Associates/Bachelor’s (science preferred) degree. Exp: 0-2 years |
The Technician I, Cell Therapy Manufacturing position is responsible for the hands-on clinical manufacturing of cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development and report to the Bioprocess and Cell Therapy Supervisor. | 12/26/2022 |
| 5482 | Ology Bioservices East Norriton, PA Bioprocess Technician II Associates/Bachelor’s (science preferred) degree. Exp: 1-3 years |
The Technician II, Cell Therapy Manufacturing position is responsible for the hands-on clinical manufacturing of cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development and report to the Bioprocess and Cell Therapy Supervisor. | 12/26/2022 |
| 5483 | Omniome Menlo Park, CA Quality Control Research Associate Bachelor’s degree in Biological/Life Sciences, Chemistry, Biochemistry, or related field. Exp: 1+ years |
Pacific Biosciences is seeking a talented Quality Control Research Associate to join our Chip NPI Systems Team. This position reports to the Manager, Senior Manufacturing Engineer, Mfg Systems. | 12/26/2022 |
| 5484 | OraSure New Brighton, MN Laboratory Technician B.Sc. or M.S. degree in Biology, Biochemistry, Molecular Biology Exp: 1+ year |
Lab Technician I will be expected to work collaboratively as part of a team. In this role, the Lab Technician I will be responsible for managing timelines, performing hands-on lab work, maintaining processing records and working in compliance with our accreditations and quality standards. | 12/26/2022 |
| 5485 | Orna Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Production, Analytics B.S. in biology, biochemistry or a related discipline is required. Exp: 1+ years |
We are seeking an exceptional researcher to join our Production team as a Research Associate/Senior Research Associate. This candidate will work closely with their manager to build our internal analytical capabilities to support the advancement of our oRNA™ platform. The ideal candidate is detailed-oriented and has experience with cell-based assays and molecular biology techniques. Ownership of strong written and oral communication skills are important to be able to effectively perform within this highly cross-functional team. | 12/27/2022 |
| 5486 | Orna Therapeutics Cambridge, MA Research Associate/Senior Research Associate, RNA Production B.S. in biology, biochemistry or a related discipline required. Exp: one year |
We are seeking an exceptional Research Associate/Senior Research Associate, RNA Production to help build and maintain our proprietary RNA production process. The ideal candidate has at least a bachelor’s degree in a biological/biochemical related field with RNA handling and process development experience. They will be able to quickly learn, troubleshoot, and integrate new protocols into existing workflows; possess strong oral and written communication capabilities; demonstrate excellent collaboration & interpersonal skills; and be adept at problem solving in a fast-paced environment. | 12/27/2022 |
| 5487 | Pacira Biosciences San Diego, CA R&D Design Engineer 2 BS in Biomechanical, Mechanical, Chemical Engineering or related engineering field Exp: 1-3 years |
Primarily responsible for the development of new products and/or the enhancement of existing products. Involved in creating concepts and modeling and drafting designs utilizing 3D CAD software. Other responsibilities include drafting of design control and design history file documents, development of test plans to assess designs, and assist in the development processes. | 12/27/2022 |
| 5488 | Pacira Biosciences San Diego, CA Microbiologist 1 BS degree in Microbiology or other life science. Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products | 12/27/2022 |
| 5489 | Pacira Biosciences San Diego, CA Microbiologist 1 BS degree in Microbiology or other life science. Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products | 12/27/2022 |
| 5490 | Par Pharmaceutical Rochester, MI Chemist I (Afternoon Shift) Bachelor of Science Degree in chemistry, chemical engineering or related field with analytical chemistry coursework required. Exp: 1+ years |
The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. May participate in investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. | 12/28/2022 |
| 5491 | Parse Biosciences Seattle, WA Lab Automation Engineer Bachelor’s degree in engineering or science; preferably biology, chemistry, or related field. Exp: 1+ years |
The Lab Automation Engineer will directly contribute to the growth and success of Parse by focusing on designing and implementing creative automated solutions. As part of a growing start-up, top candidates will have the ability to design and build fully walk-a-way automation solutions that are robust and scalable. The ideal candidate can quickly identify system limitations and leverage existing technologies to engineer solutions for risk mitigations. | 12/28/2022 |
| 5492 | Fulgent Genetics Temple City , CA Lab Technician I Bachelor’s Degree in molecular biology, genetics, or related field. Exp: 1 to 4 years |
The Lab Technician I is responsible for performing clinical laboratory test procedures following standard operating (SOP) and quality assurance (QA) procedures under general supervision. The successful candidate will be a key contributor to a team committed to clinical sequencing and diagnostic test services. | 12/28/2022 |
| 5493 | Pharmaceutics International Hunt Valley, MD QA Associate Bachelor’s degree in Microbiology or Chemistry. Exp: one (1) to three (3) years |
Witness and verify the QA functions related to manufacturing of sterile product while adhering to the cGMP ICH and USP/EP/Health Canada guidelines as written -- to ensure that the day-to-day tasks of the Quality Assurance Unit supports the overall business plan while maintaining the highest quality products and ensuring the safety, identity, strength, purity, and quality that the drug is purported to possess. Perform “Line Clearance” and “Cleaning Verification” for manufacturing and packaging operations per established Standard Operating Procedures (SOPs) and Batch/Packaging and Labeling Records’ requirements. | 12/28/2022 |
| 5494 | Plex Pharma San Diego, CA RA/SRA, Biology and Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field. Exp: 1-3 years |
The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 12/28/2022 |
| 5495 | PPD Rockville, MD Associate Scientist - mRNA Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0-2 years |
To perform the following activities for Drug Product support. This list is not all-inclusive and is subject to the needs of the project, but they will be responsible for planning and executing experimental studies in the area of mRNA lipid nanoparticle production and process optimization. | 12/28/2022 |
| 5496 | PPD Boston, MA Scientist - HPLC, GC, KF Master's degree in physical sciences (Chemistry, Analytical chemistry, Organic chemistry) or engineering. Exp: 1+ year |
As a Scientist, you will use state-of-the-art technologies to perform traditional and innovative analytical techniques and Quality-by-Design principles to develop and validate the analytical tools used to ensure the safety, efficacy and quality of the customer pharmaceutical products. As a member of the Analytical Development team, you will provide project support to the drug development programs at the customer site through laboratory techniques commonly used in the analysis of pharmaceuticals such as HPLC, GC, and KF. | 12/28/2022 |
| 5497 | PPD South San Francisco, CA Associate Scientist - Organic Chemistry Bachelor's degree or master's degree in Chemistry, Process Chemistry, or Organic Chemistry. Exp: 1+ year |
As an Associate Scientist (Research Associate), you will use state-of-the-art technologies to perform high-quality research for key pharmaceutical clients across the industry. Your problem-solving skills are an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. You will join the Small Molecule team while working onsite at the client location to support various GMP/GLP campaigns. | 12/28/2022 |
| 5498 | PPD Fremont, CA Engineer/Scientist I, QC BS/BA in Chemistry, Biochemistry, or Bioscience required. Exp: 1+ years |
Using standard operating procedures (SOP) and good manufacturing practices (GMP), the Engineer/Scientist I will perform intermediate and final release testing of filled components and finished goods kits. The Engineer/Scientist I will be responsible for all aspects of laboratory testing, such as sample receipt, data generation, product verification, data analysis and summarization, instrument operation, and all other QC lab supporting activities. | 12/29/2022 |
| 5499 | PPD Florence, SC Analytical R&D Scientist I Bachelor’s degree in chemistry or related field required. Exp: 1-2 years |
The Scientist I conducts laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Utilizes judgment in making adaptation and modifications on all assignments. Provides routine analyses in an analytical chemistry laboratory following standard practices. Performs analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results | 12/29/2022 |
| 5500 | Principia Biopharma Framingham, MA Manufacturing Associate - 2nd Shift Bachelor’s Degree in Biology, Chemistry, Biochemistry, or Chemical Engineering. Exp: 1-3 years |
As part of the Sanofi Genomic Medicine Unit organization in Framingham, the Cell Therapy Manufacturing Suite (CTMS) is responsible to support manufacturing of cutting-edge biologic drug substance material to support clinical candidate programs. The CTMS group operates in clean-room production suites under cGMP conditions to produce cell therapy products suitable for use in First in Human stage clinical trials. CTMS also interacts closely with the Quality Assurance (QA), Bioprocess Engineering, Validation, and other groups to ensure cGMPs and manufacturing schedules are maintained. Operations’ main functions are the execution of manufacturing campaigns, leading deviation investigations and managing CAPA implementation, partnering with direct manufacturing staff for enhancing and improving the manufacturing instruction set, overseeing and supporting manufacturing’s training program, and identifying and managing continuous improvement initiatives. This role is second shift: Sunday to Wednesday 3:30PM-2AM or Wednesday to Saturday 3:30PM-2AM | 12/29/2022 |
| 5501 | Principia Biopharma Swiftwater, PA Production Technician - Vaccines Associate or Bachelors' degree in Life Sciences or other relevant fields of study. Exp: no experience |
Performs production in accordance with volume fluctuation, business need, and effective procedures. Must be flexible to ensure staffing for changing business volume and needs. Works with Senior Technicians, leads, and managers to ensure operational area is running as intended to meet all operational goals. Must attend shift change daily to ensure preparedness for workday. Completes Real Time SAP transactions on all aspects of Inventory Management. Obtains and Maintains access to necessary systems as needed (SAP, RT Reports, Gibralter, HMI, SCADA access, Virtual Standards, etc.) | 12/29/2022 |
| 5502 | Principia Biopharma Swiftwater, PA Production Technician, Swiftwater, Pennsylvania - Vaccines Associate or Bachelors' degree in Life Sciences or other relevant fields of study. Exp: no experience |
You are a detail-oriented person who thrives in a fast-paced team environment. The production technician is the “heartbeat” of the vaccine manufacturing and is primarily responsible for the high quality and efficient production of our vaccines in accordance to current good manufacturing practices (cGMP) for all relevant regulatory agencies (e.g. FDA). Like all production positions at the Company, this position may require to be moved or temporarily flexed to another department/location within the Swiftwater site due to business needs. This is a 40-hour work week. | 12/29/2022 |
| 5503 | Principia Biopharma Swiftwater, PA Fill LL-2 - Vaccines Associate or Bachelors' degree in Life Sciences or other relevant fields of study. Exp: no experience |
You are a detail-oriented person who thrives in a fast-paced team environment. The production technician is the “heartbeat” of the vaccine manufacturing and is primarily responsible for the high quality and efficient production of our vaccines in accordance with current good manufacturing practices (cGMP) for all relevant regulatory agencies (e.g., FDA). Like all production positions at the Company, this position may require to be moved or temporarily flexed to another department/location within the Swiftwater site due to business needs. This is a 40-hour work week. | 12/30/2022 |
| 5504 | Principia Biopharma Swiftwater, PA Fill LL-3 - Vaccines Bachelor’s degree Exp: 1+ years |
Responsible for working inside the fill area. Performs production in accordance with volume fluctuation, business need, and effective procedures. | 12/30/2022 |
| 5505 | Principia Biopharma Swiftwater, PA Associate Scientist Manufacturing Technology Bachelor in Basic Sciences, Pharmacy, Chemical Engineering or Mechanical Engineering Exp: 1-3 years |
This position of Industrial Affairs Associate Engineer I Scientist, within the Manufacturing Technology (MTech) function of Industrial Affairs, performs activities supporting the development, validation and continuous improvement of visual inspection processes for Drug Products. The mission of the MTech function is to deliver robust and efficient processes & testing with associated knowledge to transfer to Manufacturing & QC. The Mtech function also provides daily support to manufacturing and QC toward industrial performance excellence. | 12/30/2022 |
| 5506 | ProteinSimple Austin, TX Research Associate Bachelor’s degree in biology, chemistry, biomedical engineering, or related field is required. Exp: 1-3 years |
Asuragen is seeking an outstanding BSc-level scientist to join our Research group. This is a full time position focused on developing innovative nucleic acid or protein-based technologies. This role will support new product initiatives to enable novel, multiplexed-PCR technologies that can resolve multiple classes of DNA/RNA markers or proteomics through integration of reagents, instrumentation, analysis algorithms and software. Platforms used in our laboratory include quantitative real-time PCR, digital PCR, capillary electrophoresis, next-generation and long-range sequencing. | 12/30/2022 |
| 5507 | ProteinSimple Minneapolis, MN Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Tuesday through Saturday workweek. | 12/30/2022 |
| 5508 | ProteinSimple Minneapolis, MN Research Associate, Array Manufacturing Bachelor’s degree in chemistry, biological sciences or equivalent. Exp: 0 to 2 years |
We are seeking a Research Associate for Bio-Techne’s Proteome Array Manufacturing department at our Minneapolis Headquarters. Our group supports manufacturing proteome array panels and cell isolation kits used in academic research, pharmaceutical research, and all facets of biological science including oncology, neurodegenerative diseases, stem cell research, developmental biology, etc. This individual will be trained on and work with array printing robot for microarray and perform benchtop in-process QC testing for array components. This individual will also have opportunities to collaborate with many different departments including Planning, QC, & Conjugation to support the manufacturing processes of our products. This position provides a potential for growth and career advancement within the company. | 12/30/2022 |
| 5509 | ProteinSimple Minneapolis, MN Quality Technician MLT/MLS degree, Bachelor’s degree in Biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. You will assist the QC Laboratory Manager/Supervisor with releasing products to bottle and ship, proofing labels and assay sheets. You will serve as a member of the Technical Service team by rotating through our Technical Service Department and responding to customer inquiries and complaints with the assistance of senior members of the department. This position will adhere to safety regulations. Perform additional duties as assigned. | 12/30/2022 |
| 5510 | ProteinSimple Minneapolis, MN Research Associate, Microbiology QC Bachelor’s degree in Microbiology or a related scientific field or equivalent. Exp: up to 3 years |
The responsibilities of this position are to participate in the Microbiology QC testing and reporting procedures: set up, read, and report the microbial QC bioburden and sterility testing of various sample types using culture methods that include direct plating, broth inoculation, and membrane filtration. Performance of environmental monitoring for viable microbes, particle counts, and WFI/deionized water testing, reading, and reporting. Assist with efficacy and validation testing, new procedure development, new equipment IQ/OQ and calibrations. Perform general lab duties, assist with sanitization of clean rooms, and additional duties as assigned. | 12/30/2022 |
| 5511 | Protomer Technologies Pasadena, CA Chemist / Biochemist Undergraduate degree in chemistry, biochemistry, chemical engineering with working knowledge of standard biochemistry or chemistry lab techniques. Exp: 1+ years |
The ideal candidate will have a bachelor’s or master’s degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a team player in a fast-paced research setting. The applicant will be responsible for assisting Protomer’s senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively participate and present in team meetings and is expected to contribute to the team’s progress and success. | 12/30/2022 |
| 5512 | Protomer Technologies Branchburg, NJ Research Associate-Quality Control (QC) Bioassay Master's Degree in a science related field (e.g. Biology, Biochemistry, etc.). Exp: 1 year |
Conduct routine and non-routine analyses of in-process materials, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. Perform routine QC responsibilities as needed. Apply acceptable cGMP practices during execution of all work tasks. Work independently with moderate supervisory guidance. | 12/30/2022 |
| 5513 | PsychoGenics Paramus, NJ Research Associate 1 – Surgery/Neuroscience Bachelor's degree in life sciences, neuroscience, or psychology. Exp: 1+ years |
We are looking for a highly motivated Research Associate in surgery. The successful candidate will work in a team of scientists and researchers supporting the preclinical studies using rodent models and tests. The primary responsibilities of the candidate will include but are not limited to conducting preclinical research using various surgical procedures primarily in the area of pain, animal disease model, and other drug discovery assays as needed. The candidate will be responsible for surgeries, tissue collection and drug administration, proper execution of experiments, and preliminary data analysis. The candidate must be capable of working across teams and independently. | 12/30/2022 |
| 5514 | PsychoGenics Paramus, NJ Research Associate - Neuropharmacology Bachelors or Masters degree in the biological sciences, neuroscience, or related field. Exp: 1-3 years |
We are looking for a highly motivated Research Associate in neurodegenerative disorders. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The primary responsibilities of the candidate will include, but are not limited to, dosing animals, conducting behavioral assessments for neurodegenerative disorders, and dissection and tissue collection. The candidate will be responsible for coordinating studies and the proper execution of experiments. The candidate must be capable of working both across teams and independently. | 12/30/2022 |
| 5515 | PTC Therapeutics Pennington, NJ Associate Scientist I, Analytical Development (Biological Assays) - Gene Therapy Master’s degree in biology, molecular biology, virology, biochemistry or related discipline. Exp: 0 to 3 years |
The Associate Scientist I, Analytical Development - Gene Therapy is responsible for the execution and analysis of well-established, routine assays (including, but not limited to, qPCR, cell-based and immunoassays) supporting the gene therapy analytical development organization. S/He is also responsible for communicating assay results to his/her supervisor. | 12/30/2022 |
| 5516 | PTC Therapeutics Bridgewater, NJ Associate Scientist I, Pharmacology Master’s degree in a scientific discipline. Exp: 0- 2 years |
The Associate Scientist I, Pharmacology is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC in PK/PD, inflammation, oncology and/or neurological diseases area. The incumbent, Pharmacology is also responsible for communicating experimental results to his/her supervisor and the project team. | 12/30/2022 |
| 5517 | PTC Therapeutics Mountain View, CA Research Associate II, Biology Master's Degree in a scientific discipline. Exp: 0- 2 years |
The Research Associate II, Biology is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. | 12/30/2022 |
| 5518 | PTC Therapeutics Bridgewater, NJ Associate Scientist I, Biology ( Neuroscience) Master’s degree in a biology scientific discipline. Exp: 0-2 years |
The Associate Scientist I, Biology (Neuroscience) is responsible for performing scientific experiments that contribute to research and drug discovery in the area of neuroscience. This position assists in conducting preclinical research collecting data from brain tissue of in-vivo rodent models with a concentration on the central nervous system. The candidate is responsible for generating, interpreting, and reporting data in support of novel therapeutic discovery. | 12/30/2022 |
| 5519 | DPT Laboratories San Antonio, TX Associate Scientist QC Method Validations BS in Chemistry, Biology or Biochemistry (with solid chemistry knowledge) from a four-year college or university is required. Exp: 0 – 3 years |
Perform analytical method development / validation and sample analysis. Typically, the development and/or validation will be conducted according to instructions in a protocol. The associate scientist will work with supervision from the Group Leader and/or Senior Scientist. Review the data generated during the development / validation and determine if the acceptance criteria in the protocol is being met. The associate scientist will report any failures to the Group Leader. Write standard methods of analysis. Write technical reports for method development / validation work. Write and review analytical test methods, and reports. | 12/22/2022 |
| 5520 | DPT Laboratories Morgantown, WV Chemist II Bachelor's degree (or equivalent) Exp: 0-2 years |
Perform pharmaceutical testing including, but not limited to, HPLC, GC, TLC, UV, dissolution, and IR spectroscopy. Develop and validate analytical test methods for pharmaceutical products. Critically evaluate and audit data. Write technical analytical reports and procedures. | 12/22/2022 |
| 5521 | NanoString Bothell, WA Quality Assurance Associate I Bachelor's degree in engineering, science, business, or liberal arts Exp: 0-3 years |
As a Quality Assurance Associate I, you will have a strong desire to be part of our Quality Team and assist in the administration of the Document Control and Quality Management System (QMS). As well as perform Quality Assurance (QA) product release. You will possess strong attention to detail and have a collaborative and team-oriented disposition. | 12/22/2022 |
| 5522 | Nanosyn Santa Clara, CA Associate Research Scientist B.S. in Chemistry, Biochemistry or other relevant discipline Exp: 0-2 years |
Develop new methods for the synthesis of organic molecules and prepare intermediates for the synthesis of these molecules. Apply modern techniques of organic synthesis including a variety of organic reactions at several scales, inert atmosphere techniques, thin-layer chromatography, NMR, LC-MS, HPLC, MS, flash chromatography, recrystallization, distillation, etc. | 12/22/2022 |
| 5523 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in Biology, Biochemistry or other relevant discipline Exp: 0-2 years |
We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. The ideal candidate should have good organizational skills, possess good problem solving, communication and interpersonal skills and to adapt rapidly to new challenges. | 12/22/2022 |
| 5524 | Natera San Carlos, CA Laboratory Associate: New College Graduate (2022 - 2023) BS/BA in a biological science or a related field Exp: new graduates |
Assists in analyzing specimens and maintains equipment in good operating condition. | 12/22/2022 |
| 5525 | Natera Austin, TX Laboratory Associate: New College Graduate (2022 - 2023) BS/BA in a biological science or a related field Exp: new graduates |
Assists in analyzing specimens and maintains equipment in good operating condition. | 12/22/2022 |
| 5526 | Natera Austin, TX Research Technician BS/BA in a biological science or equivalent required Exp: 1-2 years |
The Research Technician performs routine laboratory research and development services. Works with a multidisciplinary team. Under nominal direction, performs a variety of basic and general laboratory research and sample management tasks determined by the field and scope of the research project. | 12/22/2022 |
| 5527 | Natera Austin, TX Medical Laboratory Scientist BS/BA degree in Medical Technology, Biological Sciences, or a related field Exp: 0-9 yrs |
Natera is currently seeking a licensed Medical Laboratory Scientist to analyze specimens and maintains equipment in good operating condition. | 12/22/2022 |
| 5528 | Natera Austin, TX Medical Laboratory Scientist ( Recent Grads) BS/BA degree in Medical Technology, Biological Sciences, or a related field Exp: 0-9 yrs |
Natera is currently seeking a licensed Medical Laboratory Scientist to analyze specimens and maintains equipment in good operating condition. | 12/22/2022 |
| 5529 | Natera Austin, TX Instrument Support Engineer BS/BA in a biological science/biomedical engineering, similar field of study. Exp: 1 years |
The Instrument Support Engineer is responsible for the service and support of laboratory equipment and instrumentation utilized in the Operations laboratory. The scope of support includes installation, calibration, maintenance, and repair of both simple (e.g., plate sealers) and complex (e.g., liquid handling robotics) instrumentation in the laboratory. The Instrument Service Engineer will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. | 12/22/2022 |
| 5530 | NorthEast BioLab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: Entry Level |
Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices | 12/22/2022 |
| 5531 | Nektar Therapeutics Huntsville, AL Process Technician I / II (Pharmaceutical Manufacturing) For Process technician I: BS Degree in Chemistry, Biochemistry, Chemical Engineering preferred, or other science related proferred. Exp: 0-2 years |
Nektar has an exciting opportunity for a Process Technician I / II to join the Manufacturing team in our Huntsville, AL office. Day Shift: M-Th 6am - 6pm, F 6am to early afternoon. | 12/22/2022 |
| 5532 | Neos Therapeutics Grand Prairie, TX Chemist I Bachelor's degree in a science-related field or equivalent experience Exp: 1 year |
The QC Chemist I position plays a key role in the operation of the QC Laboratory. This chemist will be responsible for the timely analysis of a wide variety of samples. The QC Chemist I provide services for other departments (Production, R&D, QA, Engineering), all while operating in a state of compliance with current Good Manufacturing Practices (cGMPs). | 12/22/2022 |
| 5533 | Nephron Pharmaceuticals West Columbia, SC Microbiology Lead Environmental Monitoring Technician Bachelor’s degree preferred. Exp: 1 – 2 years |
Provides oversight and support of the environmental monitoring (EM) program during production operations. Assists Microbiology department management with environmental excursion investigations and non-conformance reports. Performs environmental monitoring activities as necessary. Assists with additional work duties or responsibilities as evident or required. | 12/22/2022 |
| 5534 | Nephron Pharmaceuticals West Columbia, SC QC Microbiology Laboratory Technician Master’s degree in Biology, Microbiology, or Life Sciences preferred. Exp: 1 year |
· Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Microbiology test methods include the following: bioburden, bacterial endotoxins, sterility, particulate matter, microbial identification, growth promotion, and vacuum decay container closure tests. · Assists in the receipt, storage, organization, and disposal of laboratory samples while ensuring compliance with FDA and DEA regulations. · Additional work duties or responsibilities as evident or required.· Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. | 12/22/2022 |
| 5535 | Nephron Pharmaceuticals West Columbia, SC Microbiology R&D Analyst I Master’s Degree in Microbiology or other science-related field Exp: 1 - 3 years |
Performs research and develops projects for both established and new products, including, but not limited to, microbiological test method validation/transfer/verification, procedures, investigations, and other non-specified projects or initiatives. Plans, organizes, and manages resources on method validation projects to assure technical quality and schedule adherence. Performs other duties as assigned or apparent. Works with different microbiological techniques and equipment, including but not limited to gram stain, turbidimetric endotoxin testing, liquid particle counter, isolator, bioburden, filtration analysis, sterility testing, aseptic process simulation, and MALDI-TOF. Performs different microbiological tests for R&D Microbiology and QC Microbiology, as needed; also understands and performs routine investigations related to Environmental Monitoring and laboratory testing. Works in a GMP environment and responsible for generating cGMP data. | 12/22/2022 |
| 5536 | Nephron Pharmaceuticals West Columbia, SC Quality Systems Scientific Specialist Tier I Bachelor’s degree preferred. Exp: 1-2 years |
Responsible for ensuring compliance with all State and Federal regulatory bodies as it pertains to the completion of Annual Product Review (APR) for all Nephron Pharmaceuticals Corporation (NPC) and Nephron 503B Outsourcing Facility (503B) drug products. Performs reviews of Standard Operating Procedures (SOP) and other formal, controlled documents for approval of any updates needed. Performs other duties as assigned or apparent. | 12/22/2022 |
| 5537 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Second Shift (Sun. - Thurs. - 2:00pm to 11:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
• Support quality control testing and research and development activities as needed. • Assists with additional work duties or responsibilities as evident or required. • Performs other duties as assigned or apparent. • Relies on instructions and pre-established guidelines to perform job functions. • Works under immediate supervision. | 12/22/2022 |
| 5538 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - First Shift (Mon. - Fri. - 8:00am to 5:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
• Support quality control testing and research and development activities as needed. • Assists with additional work duties or responsibilities as evident or required. • Performs other duties as assigned or apparent. • Relies on instructions and pre-established guidelines to perform job functions. | 12/22/2022 |
| 5539 | Nostrum Laboratories Bryan, OH Chemist I Bachelor’s Degree. Exp: 0 - 4 years’ |
Responsible for development and validation of analytical methods in support of product development and IND/NDA/ANDA filings. Perform routine wet chemical and instrumental analysis on raw materials, in-process, finished and stability products. Accurately compiles and reports data. Gather, compile and compose documents needed for regulatory submissions. | 12/22/2022 |
| 5540 | Novartis Cambridge, MA BS/MS Research Scientist, Oncology Drug Discovery - Biotherapeutics MS Exp: 0-4 years |
We are seeking a highly passionate and motivated research scientist to join our team at Novartis Oncology Biotherapeutics in Cambridge, MA. This position is ideal for someone who is creative, highly collaborative, result-oriented and wishes to combine their curiosity about oncology, cancer immunology and drug discovery to save patients’ lives. In this role, you will have the opportunities to contribute to exploratory and innovative biotherapeutic drug discovery for cancer using a variety of different assays to independently support research in this area. The successful candidate will become a crucial part of a dynamic and multidisciplinary group to interact with other functional groups and to understand the process of preclinical drug discovery, that will eventually transform the lives of cancer patients. | 12/22/2022 |
| 5541 | Novartis Cambridge, MA Research Scientist, Protein Engineering MS in biochemistry, molecular biology or related field. Exp: 0+ years |
We are looking for a passionate Research Scientist to join the team in Cambridge, MA. In this role, you will help to advance our diverse programs in NBC biologics pipeline and accelerate the discovery process. You will mainly work in lab to support all projects cross the portfolio in the protein engineering function by contributing to protein expression, purification, and characterization. | 12/22/2022 |
| 5542 | Novartis San Francisco, CA Research Scientist I, NITD Pharmacology Bachelor’s degree (B.A./B.S.) in biomedical or life sciences field preferred. Exp: 0-2 years |
The NITD Pharmacology group provides high quality in vivo research work and support to enable drug discovery research and development. We are looking for a Research Scientist I to coordinate and run in vivo research studies and projects to support the diverse and exciting project portfolio at NITD. The candidate should be action-oriented, skilled in experimental animal work, and possess a strong scientific background in order to plan, design, coordinate and perform in vivo experiments with high technical and ethical standards. The role will require an ability to work independently as well as in close collaboration with other research scientists. | 12/22/2022 |
| 5543 | Novartis Cambridge, MA Research Scientist, AAV Cell & Gene Therapy B.S in in Molecular/Cell Biology, Biochemistry or related field. Exp: 1+ years |
We are seeking a highly motivated scientist to join the Biotherapeutic Engineering and Gene Therapy (BEGT) group within NBC in Cambridge, Massachusetts. The BEGT group drives a diverse portfolio of modalities including therapeutic proteins, multi-specific antibodies, CAR-T, RNA therapeutics and AAV. Through innovative and rational protein design as well as cell and viral engineering, the BEGT group works collaboratively within NIBR to broaden the use of biologics into therapeutic applications where conventional antibodies have limitations. | 12/23/2022 |
| 5544 | Novartis Morris Plains, NJ QC Associate Scientist (PM Shift) Bachelor’s degree in chemistry, biochemistry, microbiology or other related science. MS preferred. Exp: 1 year |
Under general direction, the QC Associate Scientist will perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay and raw materials, as appropriate). | 12/23/2022 |
| 5545 | Novavax Gaithersburg, MD Laboratory Technician, Formulation - NanoFlu (Contractor) bachelor diploma Exp: 0 – 2 years’ |
We are seeking a Lab Technician to join our Formulation Department – NanoFlu, who can fulfill the job requirements listed below. This position is lab-based and will support formulation scientists in day-to-day laboratory activities, including analytical testing of samples and buffer preparation and testing. The Lab Technician is also responsible for maintaining laboratory inventory and upkeep. This position is lab-based and will be located at our Gaithersburg, MD facility. | 12/23/2022 |
| 5546 | Novavax Gaithersburg, MD Specialist I, QA/Batch Release Project Coordinator BS Exp: No experience |
We are seeking a Quality Specialist I to join our Quality Assurance as batch release and project coordinator in Gaithersburg, MD. The specialist will be responsible for support of GMP compliance with a focus on project coordination between the various QA/QC groups. The candidate will provide project coordination support, ensure organizational alignment of the QA/QC teams, and ensure all documents and the data is accurate, provide status update on all on going projects and programs. This position will require periodic weekend/evening work and travel. | 12/23/2022 |
| 5547 | Novavax Gaithersburg, MD Associate II - Analytical Development, Physicochemical, Early-Stage (Contractor) Master’s degree Exp: 1 year |
We are currently seeking an Associate II - Analytical Development (Physicochemical, Early-Stage). This contractor role is responsible for contributing to the method development, qualification, and technology transfer for analytical methods to support Early-Stage programs, including Influenza, RSV, and others. The qualified individual will bring experience in relevant analytical technologies, such as SDS-PAGE, UV-Vis, DLS, RP-HPLC, and IEX-HPLC. The position will perform in-process testing, as needed, in order to support the Process Development, Formulation Development, and Manufacturing teams, in addition to method development and qualification. This position will be located at our Gaithersburg, MD facility | 12/23/2022 |
| 5548 | NovoBiotic Pharmaceuticals Cambridge, MA Associate Scientist - Microbiologist B.S. or M.S. in Biology/Microbiology Exp: 0 to 5 years |
We are currently seeking to hire microbiologists with 0 to 5 years of experience. The successful applicant will perform microbiology lab work and data analysis to discover previously unculturable microorganisms from soil and marine environments and their identification by molecular taxonomy methods. Additional tasks will include detection of antibiotic production from these organisms and in vitro characterization of their properties, such as spectrum of activity, mechanism of action, resistance development and cytotoxicity | 12/23/2022 |
| 5549 | Novo Nordisk West Lebanon, NH Cell Therapy Associate Master’s Degree in Cell Biology, Molecular Biology or a closely related field preferred. Exp: one (1) year |
This position has the responsibility of working with senior level Scientists and manufacturing associates to execute process development, scale-up, tech transfers, and validation studies in support of manufacturing or analytics. Additionally, the role will necessitate experimental troubleshooting, GMP documentation and laboratory investigations. The position will require understanding the underlying science of the process and manufacturing equipment, or assay methods and instruments. | 12/23/2022 |
| 5550 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 12/23/2022 |
| 5551 | NuProbe Houston, TX Technician I/II (BD/Services) BA/BS, MA/MS in Biology, Biochemistry, or related field Exp: 1 – 3 years |
The Technician I/II will execute most of the Research & Development protocol activity which is vital to the success of the company. This position handles sensitive data and comes with a high degree of trust. | 12/23/2022 |
| 5552 | NuProbe Houston, TX Technician I (Innovation) BA/BS or higher in Biology, Biochemistry, Biotechnology, or a related field Exp: 0 – 3 years |
The Research Technician I – Innovation Department executes most of the research & development protocol activity which is vital to the success of the company. This position handles sensitive data and comes with a high degree of trust. | 12/23/2022 |
| 5553 | Ocean Ridge Biosciences Exton, PA QA Specialist-GLP/BIO B.S. degree in related scientific discipline Exp: >1 years |
Implement, maintain and enhance quality procedures and systems to ensure compliance with US FDA, OECD, and ICH regulatory requirements including 21 CFR Part 58, 21 CFR Part 11, 21 CFR Part 320, and other relevant guidances and publications. One of our groups also works to 40 CFR part 160. Conduct QA audits of BIO laboratories and functions including but not limited to: ongoing process, data review audits, technical report, and study independent facility / process. Provide input to method, equipment, computer validation programs. | 12/23/2022 |
| 5554 | Ocean Ridge Biosciences Exton, PA Associate Scientist, Pharmaceutical Analysis-Microbiology B.S. in Biology or related discipline Exp: 1-2 years |
Performs routine microbiology sample analysis (Bioburden, Endotoxin, Environmental Monitoring, Sterility, etc.) and a variety of tasks to support product development, ensuring agreed timelines | 12/23/2022 |
| 5555 | Ocean Ridge Biosciences Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields. Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 12/23/2022 |
| 5556 | Ocean Ridge Biosciences Concord, OH Entry Level Lab Chemist B.S. in a chemistry or related field. Exp: Entry Level |
This position is for an entry level lab chemist. The ideal candidate will help support studies of preclinical drug development in a GLP environment. | 12/23/2022 |
| 5557 | Ocean Ridge Biosciences Exton, PA Associate QC Specialist Bachelor Degree or Master Degree in Chemistry, Biochemistry or other scientific field Exp: 0-2 years |
Review of Biomarker bioanalytical data (notebook documentation, raw data, and LIMS data) for accuracy, consistency, and completeness to ensure compliance with SOPs and GLP. Review method development/qualification/validation reports and sample analysis reports including text and data for accuracy and consistency. Preparation of bioanalytical test result data tables for clinical testing reports. Review of client data transfer specifications. Prepare and transmit client data transfer tables. | 12/23/2022 |
| 5558 | Ocean Ridge Biosciences Hayward, CA Research Associate M.S. degree in related scientific discipline Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 12/23/2022 |
| 5559 | Lucigen Gaithersburg, MD Research Associate I – Manufacturing (47370) Bachelor’s degree in Biochemistry or Molecular Biology or a related field Exp: one year |
The Research Associate I position will advance LGC Clinical Diagnostics Division purpose of understanding disease by supporting the manufacture of precision diagnostic products. Support includes independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material all under GLP/GMP. | 12/12/2022 |
| 5560 | Lucigen Cumberland, ME Manufacturing Chemist I (47324) Bachelors degree in life science field or other related science or medical curriculum Exp: no experience |
The Manufacturing Chemist I fulfils the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 12/12/2022 |
| 5561 | Lucigen Petaluma, CA Therapeutic Production Chemist I - Day Shift (46932) Bachelors of Science in a relevant STEM field Exp: 1 or more years’ |
The Therapeutic Production Chemist I perform routine oligonucleotide manufacturing processes in the LGC Axolabs Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophlization of oligonucleotides, | 12/12/2022 |
| 5562 | Lucigen Charleston, SC QC Chemist (42600) Bachelor of Science in chemistry degree or equivalent is preferred Exp: one-year |
This is an entry QC chemist position where one is responsible to make check standards, routine instrument maintenance and operation of GC/MS, GC/FID, HPLC, and UHPLC/MS, validating manufactured products in a timely manner. Attention to detail, teamwork, the ability to thrive in a fast-paced work environment and organizational skills are necessary to excel in this position. | 12/12/2022 |
| 5563 | Lucigen Petaluma, CA Therapeutic Production Technician I - Entry Level- Day Shift (47172) Bachelors degree preferred with a Science background Exp: 1+ years' |
The Therapeutic Production Technician will support oligonucleotide manufacturing processes in the LGC Axolabs Petaluma Therapeutic GMP suite. Activities include: daily calibration of instruments, stocking materials, cleaning and maintaining labware. | 12/12/2022 |
| 5564 | Lucigen Petaluma, CA Therapeutic Production Chemist - Night Shift (47170) Bachelor of Science in a relevant STEM field is required. Exp: 1+ years' |
The Therapeutic Production Chemist will perform routine oligonucleotide manufacturing processes in the LGC Axolabs Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophilization of oligonucleotides. | 12/12/2022 |
| 5565 | Lung Biotechnology Research Triangle Park, NC Bioprocess Associate I/II - Cell Biology, Bioprocess Development Bachelor’s Degree in Arts/Sciences (BA/BS) in biology, cell and molecular biology, biomedical sciences, biomedical engineering, biomanufacturing, or a Exp: Bioprocess Associate I: 1+ years |
Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. | 12/12/2022 |
| 5566 | Lung Biotechnology Manchester, NH Research Associate I – Cellularization Bachelor’s Degree in Arts/Sciences (BA/BS) in Cellular Biology, Developmental Biology, or Biomedical Engineering or related field Exp: 1+ years |
The Research Associate I - Cellularization (OMG) will support the development and characterization of bioinks for 3D printing scaffolds for lung tissue engineering. They will design and print 3D diagnostic models to test bionks for compatibility with different lung cell types. | 12/12/2022 |
| 5567 | Lung Biotechnology Manchester, NH Associate Process Engineer/ Process Engineer, Biomaterials Bachelor’s Degree in Arts/Sciences (BA/BS) in materials science, chemistry, chemical, mechanical or biomedical engineering (or equivalent) Exp: 1+ years |
The Associate Process Engineer, Biomaterials (OMG) will be responsible for scaling up and experimenting with large batches of ink to support process and product feasibility goals. This position will also be responsible for periodic quality control (QC) testing. | 12/12/2022 |
| 5568 | Lykan Bioscience Hopkinton, MA QC Analyst, Microbiology Certificate in Biotechnology or Bachelor's degree in scientific discipline preferred Exp: 0-7+ years' |
The Quality Control Analyst environmental monitoring will be responsible for collection of environmental samples in clean room areas to support manufacturing operations, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. | 12/12/2022 |
| 5569 | Machaon Diagnostics Berkeley, CA Clinical Laboratory Assistant B.A./B.S with coursework in chemistry, biochemistry, immunology, molecular biology, statistics and related subjects required. Exp: 6 months or more |
Demonstrate proficiency and understanding of standard clinical laboratory practices. Review requisitions, orders tests and processes specimens in preparation for laboratory procedures. Perform general laboratory maintenance tasks including preparing reagents, re-stocking consumables and washing glassware. Assist with quality control and quality assurance paperwork. Assist with clinical trials including completion of Institutional Review Board documentation, subject recruitment, screening, and management, and performance of research related testing. Design and revise forms and protocols. Adhere to Machaon policies and procedures as directed by the supervisor, manager or medical director. Interact with patients, subjects, visitors, physicians, and coworkers in a professional and courteous manner. | 12/13/2022 |
| 5570 | Marker Therapeutics Houston, TX Cell Therapy Manufacturing Technician BS, MS in Biology or a related science Exp: 1-5+ years |
Marker Therapeutics is seeking a cell therapy technician for its manufacturing group to support its ongoing efforts to develop immunotherapies for the benefit of patients with cancer. This position will work under the guidance of the Senior Director of CMC and perform assigned responsibilities to support the company’s product manufacturing process and process improvement initiatives. | 12/14/2022 |
| 5571 | Matica Biotechnology College Station, TX Manufacturing Associate AS/BS in Biotechnology, Biology, Chemistry, or equivalent. Exp: 0-2 years |
The successful candidate for manufacturing associate will execute the daily manufacturing schedule communicated by the Manufacturing Supervisor to include but not limited to cell expansion, bioreactor operations and purification techniques (TFF and Chromatography) for viral vector manufacturing processes. | 12/14/2022 |
| 5572 | Medtronic Bedford, MA Quality Engineer II Master's Degree in Engineering or Technically Related discipline. Exp: 0 years |
Medtronic Cardiac Ablation Solutions Group (CAS) is searching for a Quality Engineer II to join our growing Quality Operations team in Bedford, MA. In this role, you will be responsible for various programs within our Quality Management System and for driving day-to-day compliance in the development and manufacturing of leading-edge medical devices. We are looking for bright, hands-on individuals who are interested in making a difference in a dynamic and exciting entrepreneurial environment. The ideal candidate will be a motivated individual looking to grow professionally in a fast-paced environment. Strong analytical skills, excellent knowledge of theoretical and practical fundamentals, and a solid ability to work on multiple projects simultaneously are required. | 12/15/2022 |
| 5573 | Medtronic Santa Ana, CA Microbiologist II Master's Degree in Microbiology or Related discipline Exp: 0 years |
In this exciting role as a Microbiologist-Sterilization II you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 12/15/2022 |
| 5574 | Medtronic Irvine, CA Microbiologist-Sterilization II - Irvine, CA Advanced degree in science or technical field Exp: 0+ years |
In this exciting role as a Microbiologist-Sterilization II you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 12/15/2022 |
| 5575 | Medtronic North Haven, CT Chemist II Master's Degree in Chemistry, Biology, Material Science, or related technical discipline Exp: 0 years |
The chemist will be primarily responsible for performing Extractable and Leachable Extractions and Inductively Coupled Plasma- Mass Spectrometry (ICP-MS) data analysis and testing support in an analytical chemistry lab. The position has responsibility for project-based sample preparation, operation of ICP-MS instrumentation, data processing, and quantitation for chemical characterization in accordance to ISO10993. The role functions as part of an analytical chemistry team that works under ISO 13485 and ISO 17025 Quality Management Systems. | 12/15/2022 |
| 5576 | Medtronic Santa Rosa, CA R&D Engineer II - Transcatheter Heart Valve Therapies Advanced degree in Engineering. Exp: 0+ years |
This is an exciting opportunity to join Medtronic's Structural Heart business unit to work with a dedicated team focused on the development and expansion of our new transcatheter heart valve replacement system. In this role, the Engineer II will be working on the delivery system team to develop, qualify, and commercialize the device. | 12/15/2022 |
| 5577 | Medtronic Boston, MA Systems Engineer II - Surgical Robotic Master's Degree in Engineering or Technically Related discipline. Exp: 0 years |
This position is in the Boston, MA office, reporting to the Integration Site Lead in the Systems Integration Center of Excellence. The System Engineer II is a technical individual contributor role within the R&D engineering team that is developing Medtronic’s Robotic Assisted Surgical Device (RAS). This candidate shall have an engineering mindset and contribute to logistics that support enabling development teams to utilize the capital equipment on a variety of project variants. This role will include aspects of fleet repairs, inventory management, planning, tracking, allocation of hardware and documentation related to the robotic system and its components. | 12/15/2022 |
| 5578 | Merieux NutriSciences Salt Lake City, UT Microbiologist Bachelors preferred Exp: One (1)- 2 years |
We are looking for a Microbiologist in 1945 Fremont Drive, Salt Lake City, UT 84104 USA. Your mission will be to: Follow appropriate methods and SOPS on all tasks. Maintain quality control records Read, calculate, record data in Laboratory Information Management System Perform rapid test methods Perform confirmation tests on suspect samples to identify the strain of bacteria Read, enter and evaluate process control samples Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities Support root cause analysis investigations and suggest appropriate corrective actions Weigh appropriate amount of sample and pour correct agar to begin analysis procedures. Write identification onto plates so that client and sample number can be tracked | 12/15/2022 |
| 5579 | Merieux NutriSciences Cypress, CA Microbiology Technician Bachelor’s degree required. Exp: no experience |
No previous laboratory experience is required - we will provide full training. ▪Read plates and tubes, as required, to determine the number of organisms in the sample ▪Record findings on worksheet for verification ▪Write identification onto plates so that client and sample number can be tracked ▪Pipette sample solution into tubes or plates according to the analysis process being performed ▪Pour the agar into plates or tubes to begin the growth process ▪Prepare sample for analysis by recording, weighing, and blending ▪Collect plates and place them in the incubator for the specified amount of time and temperature ▪Prepare media and broth for use in pathogen testing as required ▪Sterilize materials needed for analysis. Autoclave plates before discarding ▪Perform food poisoning, pH and other analysis tests on sample when requested by the client ▪Ensure that media and materials are prepared for the next testing sequence ▪Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities ▪Set up equipment and materials needed for analysis | 12/16/2022 |
| 5580 | Merieux NutriSciences Crete, IL Microbiologist Bachelors preferred. Exp: One (1)- 2 years |
▪Follow appropriate methods and SOPS on all tasks.Maintain quality control records ▪Read, calculate, record data inLaboratory Information Management System ▪Perform rapid test methods ▪Perform confirmation tests on suspect samples to identify the strain of bacteria ▪Read, enter and evaluate process control samples ▪Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities ▪Support root cause analysis investigations and suggest appropriate corrective actions ▪Weigh appropriate amount of sample and pour correct agar to begin analysis procedures.Write identification onto plates so that client and sample number can be tracked▪Follow appropriate methods and SOPS on all tasks.Maintain quality control records ▪Read, calculate, record data inLaboratory Information Management System ▪Perform rapid test methods ▪Perform confirmation tests on suspect samples to identify the strain of bacteria ▪Read, enter and evaluate process control samples ▪Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities ▪Support root cause analysis investigations and suggest appropriate corrective actions ▪Weigh appropriate amount of sample and pour correct agar to begin analysis procedures.Write identification onto plates so that client and sample number can be tracked | 12/16/2022 |
| 5581 | Merieux NutriSciences Crete, IL Chemist I Bachelors preferred. Exp: One - two years |
Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. Wash glassware as needed and prepare samples as needed. Prepare standards or reagents that are needed for the analysis procedure. Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. | 12/16/2022 |
| 5582 | Merieux NutriSciences Crete, IL Chemist III Masters degree. Exp: 1-2 years |
Purpose (Objective): The incumbent is responsible for performing chemical analysis on food, pharmaceutical, and other sample. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the sample to obtain the required results. The incumbent observes daily activities of departmental personnel ranging from receiving to reporting of results and ensures that analysis is performed correctly. | 12/16/2022 |
| 5583 | Meso Scale Discovery Rockville, MD Chemist BS in Chemistry, Biochemistry or related field. Exp: 1 year |
Chemist needed to: perform organic syntheses to manufacture compounds for use in company products; monitor reactions in-process using HPLC and TLC to determine progress; purify reactions using size-exclusion chromatography and recrystallization to measure process yields; analyze purified products by HPLC and TLC to determine levels of purity; interpret NMR and MS spectra to determine identity of synthesized compounds; operate lyophilizers and automated crimping and labeling equipment to produce lyophilized vials. | 12/16/2022 |
| 5584 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1 - 3 years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. | 12/16/2022 |
| 5585 | Meso Scale Discovery Gaithersburg, MD Research Associate, Recombinant Antibodies Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1 - 3 years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory position to apply various molecular biological tools and techniques to develop new recombinant antibodies and other proteins. | 12/16/2022 |
| 5586 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1 - 3 years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. | 12/16/2022 |
| 5587 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1 - 3 years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. | 12/16/2022 |
| 5588 | Meso Scale Discovery Gaithersburg, MD Cell Culture Specialist I Cell Culture Specialist I Bachelor's degree in Biology, Chemistry, Biotechnology, Engineering or a related field . Exp: six months |
This position is responsible for the production of cell-based products including but not limited to hybridoma antibodies and recombinant antibodies. | 12/16/2022 |
| 5589 | Mevion Medical Systems Littleton, MA Electrical Manufacturing Engineer, Entry/Mid level Bachelor of Science degree in Electrical Engineering, Robotics Engineering, or equivalent. An advanced degree is desirable. Exp: 1+ years |
The Electrical Manufacturing Engineer will Provide manufacturing engineering support in the design, manufacture, installation, and acceptance testing of a medical proton particle accelerator and its support systems. | 12/16/2022 |
| 5590 | Microbiologics Saint Cloud, MN Senior Research and Development Associate, Saint Cloud Master’s degree in related field Exp: 0-2 years |
Microbiologics, a leader in providing external controls for molecular diagnostic assays is seeking to expand its Product Development Team with the addition of an experienced Senior R&D Associate trained in molecular biology and assay diagnostics. The Senior Associate will design, lead, perform and report on experiments using microbiology and molecular techniques leading to new products or process improvements in an FDA-QSR and ISO13485 compliant organization. The ideal candidate will have experience in product commercialization, expert knowledge of concepts (such as nucleic acid extraction, real time PCR and Digital PCR), and a high level of scientific creativity and technical proficiency. | 12/16/2022 |
| 5591 | Miromatrix Medical Eden Prairie, MN Per Diem Technician - Part Time Cell Isolation Team Associates degree or working on BS in one of the Life Sciences disciplines including Biology, Cell Biology, or Microbiology Exp: 0+ - 2 years |
Assists with tissue/sample production according to established plans and maintains records in compliance with Miromatrix policy and GMP. Assists in testing and quality control of cell or tissue samples. Works directly with supervisor, team lead, and other team members during production and independently for most testing and quality control once fully trained. | 12/16/2022 |
| 5592 | Moderna Therapeutics Cambridge, MA Research Associate, Infectious Disease Research Master’s degree in Biochemistry, Cell biology or related discipline. Exp: 0-1 years |
Moderna is seeking a talented and experienced Research Associate to work on protein production, purification and characterization to help discover and develop new mRNA vaccine antigens to prevent and treat infectious diseases (ID). The candidate will work with collaboratively internal teams to help advance the infectious disease mRNA vaccine portfolio. Research will involve antigen discovery, characterization and evaluation for in vitro and in vivo analyses, including production of antigens for clinical biomarker readout. The candidate will work in a matrixed working environment, interact and facilitate collaborations with internal and external research partners. Applicants should be outstanding at lab-based research, a collaborative team member and an excellent communicator. | 12/16/2022 |
| 5593 | Moderna Therapeutics Norwood, MA Research Associate in LNP Process Science BS or MS in Bio/Chemical Engineering, Chemistry, or closely related field Exp: 0-2 years |
Moderna is seeking a highly skilled and motivated process development scientist to develop lipid nanoparticles (LNPs) within the Technical Development organization. This role will develop, scale-up, and transfer new and improved production processes for Moderna’s first-in-class messenger RNA (mRNA) based medicines to enable our clinical supply and late-stage development. | 12/16/2022 |
| 5594 | Moderna Therapeutics Norwood, MA Research Associate, Process Development Bachelors in biochemistry, chemistry, molecular biology, chemical engineering, biological engineering or a related discipline. Exp: 0‑2 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. We’re seeking a highly skilled and motivated Research Associate to reside in Moderna’s Technical Development organization in Norwood, MA. This is a lab-based role that will support the early phase process development of Moderna’s mRNA-based medicines to enable our clinical supply and pipeline. The applicant should have strong communication and collaboration skills. | 12/16/2022 |
| 5595 | Moderna Therapeutics Norwood, MA Engineer I, Process Development BS/MS in Chemical Engineering, Chemistry, Biochemical Engineering, Biochemistry or closely related field. Exp: 0-3 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. We are seeking a Bioprocess scientist or engineer to reside in Moderna’s Technical Development organization in Norwood, MA. Our team’s goal is to envision, pilot, scale, characterize, transfer, and validate robust commercial GMP manufacturing processes. We seek applicants who are proactive, enthusiastic, and show a passion for process development. | 12/16/2022 |
| 5596 | Moderna Therapeutics Norwood, MA Associate Specialist, Manufacturing Bachelor's Degree in Engineering or Life Sciences is preferred. Exp: 1-3 years |
This Associate Specialist will be part of a cohesive team responsible for producing high quality mRNA-based medicines for commercial production and evaluation in human clinical trials. The Associate Specialist uses expert knowledge of cGMP regulations and biopharmaceutical production processes to support day to day operational support through deviation and CAPA writing with a focus on but not limited to Commercial Lipid Nanoparticle Manufacturing. | 12/16/2022 |
| 5597 | Moderna Therapeutics Norwood, MA Associate Specialist, Manufacturing (Batch Specialist) Bachelor's Degree in Engineering or Life Sciences is preferred. Exp: 1-3 years |
The individual in this role will be part of a cohesive team responsible for producing messenger RNA for commercial production or for evaluation in human clinical trials. This position will specifically focus on batch readiness and batch close out activities. The Manufacturing Associate Specialist uses knowledge of manufacturing biopharmaceutical unit operations, quality systems and digital infrastructure to as act as a batch readiness and close out lead for the team. The Specialist will be a key team member maintaining the production schedule, managing batch record close out and Manufacturing owned actions supporting product disposition. They will leverage knowledge of cGMP regulations to support some investigations and improvement initiatives within manufacturing operations. Additional functions include acting as a responsible liaison between the Manufacturing group and other partner groups (Facilities, Supply Chain, QA, etc.) This role will also work cross-functionally to assist in planning manufacturing activities, maintenance and calibration of equipment and instruments and provide oversight of batch close out work such as batch record review and completion. The Specialist must be technically capable with a good theoretical comprehension of general biopharmaceutical manufacturing equipment, principles and processes. The successful candidate must have a good understanding of current GMP and safety standards and be able to apply this knowledge in a GMP environment. | 12/16/2022 |
| 5598 | Genomatica San Diego, CA Research Scientist I Bachelor’s, Masters, or Doctorate in Chemistry, Biochemistry, Biology or related fields Exp: 0-2 years |
Genomatica is seeking a scientist with experience in analytical chemistry or a related field to work as a member of the Analytical Sciences team. The team is responsible for quantitative analysis of fermentation, and DSP impurity/purity profiles using HPLC, GC and IC analytical systems. Furthermore, the scientist would be responsible for identifying unknowns in these materials and for developing quantitative and qualitative methods for analysis thereof. The results generated will provide valuable data and insights for our internal project development and bioprocess development and optimization as well. You will perform lab duties under the supervision and mentorship of senior analytical personnel. You will contribute to multiple projects daily and ultimately to the long-term success of the company. You will utilize a variety of analytical chemistry techniques to support and help advance Genomatica strain engineering and process technology platforms. | 12/6/2022 |
| 5599 | GenScript Piscataway, NJ Research Scientist – Automated Process Development Ph.D., MS Biology/ Biochemistry/ Molecular Biology/ Biomedical Instrumentation/ Bioengineering Discipline or related subjects Exp: 1 year (for MS candidates) |
We are looking for a Research Scientist – Automated Process Development to support the key high throughput molecular biology reagent production needs in the US Molecular Biology/ Reagent services business unit. | 12/6/2022 |
| 5600 | Glaukos San Clemente, CA MANUFACTURING TECH I/II, 2ND SHIFT Bachelor's degree in science or engineering Exp: 0-2 years' |
Prepare components and build assemblies Prepare bulk drug formulations | 12/7/2022 |
| 5601 | Glaukos San Clemente, CA ENGINEER I/II Master’s degree in Mechanical, Biomedical, Chemical Engineering or equivalent; Bachelors’ degree in Mechanical, Biomedical, Chemical Engineering or e Exp: MS: 0-2+; BS: 1-3 years |
Developing manufacturing processes, production scale-up, and sustaining support Developing creative solutions to manufacturing problems Development and execution of process, equipment, and product validations/qualifications Ensuring engineering deliverables are accurately generated, via 3D CAD models and 2D CAD drawings for assembly tools, fixtures, and clinical supplies Leading manufacturing related project teams (i.e. engineers, technicians, and manufacturing staff) with a focus on meeting manufacturing requirements while taking a high quality/cost effective approach. | 12/7/2022 |
| 5602 | Global Pharma Tek San Diego, CA Scientist 1, Analytical Chemistry Development B.S. Degree in Chemistry, Engineering, or Life Science Exp: 1 to 3 years |
The Quality Control Chemist I conducts various analytical testing of raw materials, semi-finished intermediates, finished products, and new compounds/products in various stages of design and development to characterize and determine quality. | 12/7/2022 |
| 5603 | Global Pharma Tek Charles City, IA Scientist BA/BS in Science related Field Exp: 0 - 1 year |
Daily testing of samples received from production. Timely completion of tests to meet the established testing time. Following GMP documentation guidelines. The colleague should have ability to follow detailed instructions and have basic problem solving skills and ability to trouble shoot issues that may arise when testing. Colleague must be willing to contribute to the teams productivity and overall goals. | 12/7/2022 |
| 5604 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Microbiology Technician (2nd and 3rd Shift) Bachelor’s degree in microbiology or a related field Exp: 0-2 years’ |
The Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. | 12/7/2022 |
| 5605 | Grifols Research Triangle Park, NC Assoc. Research Scientist II/Sr. Assoc. Research Scientist I Senior Associate Research Scientist I: Degree must be within a relevant field: (Biology, Biochemistry, Chemistry, or Toxicology) Masters; Associate Re Exp: SARSI: + 1 year ; ARSII: MS 0 years; BS 1-2 years. |
The selected candidate provides analytical testing support for process characterization, developmental stability studies, and release of preclinical or clinical batches for internal research projects. The individual selected for this position will conduct testing of non-routine sample types in support of process development, characterization, and/or validation and compile data for the generation of multi-user interactive analytical databases. The analyst may participate in development, implementation and validation of new analytical techniques. | 12/7/2022 |
| 5606 | GRO Biosciences Cambridge, MA Research Associate/Sr RA, Chemistry Expansion MS degree or BS/BA degree in biology, microbiology, biotechnology, biological engineering, or related field Exp: MS: 0 year; BS: 1 year |
The selected candidate for this position will work within the Chemistry Expansion division, enabling the scalable incorporation of new amino acids into proteins. Major job responsibilities include development and screening of translation machinery for new amino acids, and general engineering of ribosomal translation. Day-to-day activities include design and execution of experiments in conjunction with other team members. Diligence, transparent communication, and record keeping will be critical skills to enable success in this position. Your creativity and ingenuity will be crucial to driving GRObio’s research priorities optimizing strain performance and expanding the amino acid alphabet to create differentiated products. | 12/7/2022 |
| 5607 | GlaxoSmithKline King of Prussia, PA Associate Scientist- Bio Pharm Drug Substance Process Development Master's degree (Chemical Engineering, Biochemistry, Chemistry or Biology) Exp: 0 - 1 year |
As an Associate Scientist in Downstream Process Development, you will be a member of a highly skilled team of scientists and engineers responsible for the evaluation and optimization of purification processes. You will be involved in all aspects of the development of purification processes including initial process screening, optimization and characterization, scale-up and tech transfer to clinical manufacturing and/or commercial manufacturing partners for therapeutic proteins including monoclonal antibodies, and antibody-drug conjugates. Your primary focus will be on the bench-scale laboratory development of purification unit operations such as column chromatography (affinity, ion exchange, HIC, mixed mode, etc.), ultrafiltration, depth filtration and continuous centrifugation. Although predominantly lab-based, the role also involves verbal and written communication and requires good organization. Both individual and team working are required and therefore the role will suit a scientist with good interpersonal skills, self-motivation and an open mindset. | 12/7/2022 |
| 5608 | GlaxoSmithKline Rockville, MD Associate Scientist Bachelor's degree (biotechnology, molecular biology, biochemistry, molecular, bacteriology, molecular, microbiology). Exp: One or more years |
As Associate Scientist within the Molecular Analytics platform, you will be in charge of implementing, designing and developing methods for the detection and quantification of nucleic acids based on up-todate nucleic acid technologies (NAT) and, in particular, methods aiming at characterizing plasmids (topology, conformation, sequence, quantity, etc.), mRNA Drug Substances (content, integrity, identity) and mRNA-LNP Drug products (monovalent and multivalent), used for production of mRNA vaccines. The use of direct nucleic acid quantification methods (e.g. CRISPR-based assays, digital counting through optical barcodes, branched DNA assays, etc.) will part of the activities of the hired Scientist. | 12/7/2022 |
| 5609 | GlaxoSmithKline Hamilton, MT QC Systems Support Specialist Bachelor's Degree in a scientific discipline Exp: 1+ years |
As a QC Systems Support Specialist, you will manage non-testing laboratory support systems and processes for QC, including: Maintaining SAP Modules, Master Data/Monograph Creation, Compendial Review, Equipment Qualification/Lifecycle, and Method Validation/Transfer. In this role, you will serve as a Lead Investigator for select QC Unplanned Events, as well as change coordinator for selected QC Change Controls. In addition, you will author QC Technical Documents, such as validation and trend reports and provide data for annual PQR. | 12/7/2022 |
| 5610 | GlaxoSmithKline Rockville, MD Associate Scientist, Physical & Chemical Analytics Bachelors/Masters in Sciences/Engineering discipline Exp: BS: 1-4 years ; MS: 0-2years |
In this role you will be the Strategic Insight Business Partner to the Global RSV Adult Vaccine Commercialization Leader (VCL). This role will provide YOU the opportunity to deliver key activities to progress YOUR career.In this role you will be the Strategic Insight Business Partner to the Global RSV Adult Vaccine Commercialization Leader (VCL). | 12/7/2022 |
| 5611 | HelixBind Boxborough, MA Formulation Technologist Certificate, Associate’s or Bachelor’s degree in a science or engineering discipline Exp: 0-5 years’ |
We are seeking a talented and motivated individual to join our R&D Team as a Formulation Technologist. This is a great time to join our team. The position offers the exciting opportunity to grow along with the Company as we take our initial product through FDA clearance and market launch while, in parallel, build out our pipeline of impactful syndromic diagnostic assays. | 12/8/2022 |
| 5612 | Heron Therapeutics San Diego, CA Senior Research Associate I-III M.S. in chemistry or related subject. Exp: 1+ years |
The qualified candidate will join the Pharmaceutical Sciences team to develop, qualify, and implement characterization and quantitative analysis of Heron products, including polymers, oligomers, and small molecules. Desirable skills include mass spectrometry, HPLC, GC, and other physico-chemical methods. | 12/8/2022 |
| 5613 | Hexagon Bio Menlo Park, CA Research Associate/Senior Research Associate, Chemical Biology BSc or MSc in chemistry, biochemistry, chemical biology, microbiology, molecular biology, or a related discipline Exp: 1+ years |
We are searching for a high-caliber Research Associate who has experience with modern molecular biology, genetic engineering, and chemical analysis. The ideal candidate is excited to solve scientific questions, interested in discovering new therapeutics, and energized by working with a dynamic, data-driven team. We would like team members to be thoughtful, meticulous, well-organized, team-oriented, and fully engaged in the execution of the workflow. | 12/8/2022 |
| 5614 | Hexagon Bio Menlo Park, CA Research Associate/Senior Research Associate, Fungal Microbiologist B.S. or M.S. in microbiology, plant pathology, microbial ecology or other related field Exp: 1+ years |
We are searching for a highly motivated Research Associate on the Sequence the Earth team. You’ll play a critical role in Hexagon Bio’s efforts to unlock the biosynthetic potential of the kingdom Fungi. Your primary contributions will include: culturing, documenting, and maintaining a diverse collection of fungi. You’ll contribute to both manual, and robotics-aided high-throughput culturing and genomic DNA/RNA extraction workflows, manage strain-frozen stocks and activation and enhance the efficiency and quality of these processes. You’ll work closely with our Fungal Genetics team, Automation Engineers, and Software Engineers to develop methods vital to these tasks. Applicants with a strong handle on microbiology and the diversity of phenotypes and growth habits of filamentous fungi are encouraged to apply. This is an ideal position for someone with experience in an academic or industrial microbiology laboratory setting culturing diverse fungi from existing collections and/or nucleic acid extractions from filamentous fungi. | 12/8/2022 |
| 5615 | ICU Medical Austin, TX Analyst I, Chemistry - (22301793) Bachelor’s Degree is required: Chemistry, Chemical Engineering, or Chemical Science Exp: 0-2 year |
The Chemistry Analyst I will work under direct supervision or be partnered with an experienced analyst to perform wet chemistry analyses, preparation of reagents, standardization of solutions, and instrumentation testing and documentation in a cGMP environment. May be cross-trained to work in other laboratory areas as dictated by the needs of the department. | 12/8/2022 |
| 5616 | Invitae San Francisco, CA DNA Extraction Technician Bachelor’s degree in clinical laboratory studies or equivalent science related studies Exp: 1+ years |
Thur-Mon, 3:00pm-11:30pm We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work at our San Francisco location as well as ability to work overtime and off-schedule days as needed. | 12/8/2022 |
| 5617 | Invitae San Francisco, CA Lab Technician Bachelor's degree in clinical laboratory studies or equivalent science related studies, Exp: 1+ years |
Sunday - Thursday, 3:00pm - 11:30pm We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while aligning with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. The team's culture is one in which direct and consistent feedback can be given and taken; we encourage honest and open communication and constructive feedback. We rely on team members to work with a sense of urgency and with a goal of putting the team above the individual. We prioritize transparency and continuous process improvement to contribute towards the highest level of patient care. | 12/9/2022 |
| 5618 | Ionis Pharmaceuticals Carlsbad, CA Research Associate / Senior Research Associate, Neurology Research M.S Exp: >1-3 years |
onis Pharmaceuticals is seeking a highly qualified individual to join our Neurology research group. Our Neurology research group is currently applying Ionis’ antisense oligonucleotide (ASO) technology to develop treatments for various neurodegenerative diseases. The ideal candidate is self-motivated, excellent communicator, strongly committed to the scientific process, and capable of working independently as well as collaboratively in a fast-paced environment with strict deadlines. Key responsibilities include execution of in vivo and in vitro studies, performing assays, analyzing and presentation of data to support drug discovery efforts. This is an individual contributor position with most of the work being performed in a laboratory setting. | 12/9/2022 |
| 5619 | Ivenix Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift (Chemistry) B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 12/9/2022 |
| 5620 | Ivenix Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 12/9/2022 |
| 5621 | JOINN Biologics Richmond, CA Analyst I, II or Sr Analyst - QC Analytical MS Exp: 0-2 years |
We are searching for a highly motivated Quality Control Analyst who preferably has a minimum of 2 years of experience working in cGMP quality control laboratory environment with expertise in wet and protein chemistry to join our team. The candidate will be responsible for the qualification and execution of analytical laboratory tests and evaluations of product performance and processes in the Quality Control Department, in accordance with approved methodologies, policies, and associated regulations. | 12/9/2022 |
| 5622 | JOINN Biologics Richmond, CA Associate I - QA Bachelor’s degree in a scientific and/or technical discipline related to biology, biotechnology, chemistry or pharmaceutics. Exp: • 1+ years |
The QA Associate will be responsible for the overall strategy and oversight of JOINN Biologics Quality and Compliance for API and final product. This candidate will be writing protocols and must have strong communication, technical writing, and statistical analysis skills. | 12/9/2022 |
| 5623 | KBI Biopharma Louisville, CO Research Associate I/II B.S. Exp: 0-2 years |
Open position available in the biophysical characterization core of the rapid analytics testing group. Responsible for analytical testing of client samples. Testing may include using client-based methods or some method development. Ideal candidate is able to quickly and accurately generate results. Technical writing skills are a plus. | 12/9/2022 |
| 5624 | KBI Biopharma Durham, NC Manufacturing Specialist - Downstream Master’s degree in a related scientific or engineering discipline preferred Exp: 0+ year’s |
The manufacturing specialists on the operations team will support the startup and ongoing manufacturing operations at a new biopharmaceutical manufacturing facility. The individual will report to the associate director of manufacturing in support of upstream, downstream, or manufacturing support. The individual will be responsible for supporting equipment and operations for the upstream, downstream, and/or manufacturing support teams. The ideal candidate will have experience supporting the startup and ongoing operations for a commercial GMP mammalian cell culture facility. Expertise using single-use bioprocessing equipment and materials is highly desired. Experience with cell culture, chromatography, filtration, and/or solution preparation operations is required for Specialist I and higher levels. | 12/9/2022 |
| 5625 | KBI Biopharma Boulder, CO Research Associate I/II Bachelor of Science Degree in Biochemistry, Molecular Biology, Biopharmaceutical Development or related disciplines Exp: 1-3 years |
Perform contract testing services, including in-process and GMP release testing, GMP stability testing, method transfer activities, and qualification/validation activities for monoclonal antibodies, recombinant proteins, and peptides. | 12/9/2022 |
| 5626 | KBI Biopharma Durham, NC Microbiology Associate I/II Bachelor’s/Master’s degree in Microbiology, Biology or related technological field of science. Exp: BS: 1-2 years; MS: 0-1 years |
Sunday, Monday, Tuesday, Wednesday (Sun-Wed) Position. Second shift 1pm-11:30pm. This position is eligible for a shift differential. The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. | 12/9/2022 |
| 5627 | KBI Biopharma Durham, NC Manufacturing Associate I/II-Upstream (Nights) Manufacturing Associate I: Bachelor’s degree in a related scientific or engineering discipline. Exp: 0-2 years’ |
This position is on a 2-2-3 schedule, with the hours 7p-7a. The Manufacturing Associate I/II – Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II – Upstream must follow the instructions depicted in SR’s, EPR’s, BR’s, SOP’s and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including ‘Right the First Time’ (RFT). Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. | 12/9/2022 |
| 5628 | KBI Biopharma Durham, NC In Process Research Associate BS in scientific discipline or equivalent Exp: 0-2 years’ |
KBI Biopharma, Inc. is a contract services organization committed to reducing process development time, decreasing production cost and increasing speed of development for biopharmaceuticals. We are seeking an In-Process Support Associate with strong protein chemistry background to perform cGMP in-process analytical support. These services include in-process and release testing for drug substances manufactured internally. | 12/9/2022 |
| 5629 | Key Tech Baltimore, MD Electrical Engineer (Full-Time & Intern Positions) BS or MS Electrical Engineering degree from leading university/college Exp: Up to five years |
We’re actively hiring for full-time engineers as well as spring, summer and fall interns (electrical, computer, and mechanical) with competitive well paid salaries and benefits. Our interns work on real engineering challenges from day one. Everyone who starts at Key Tech jumps right into interesting, creative high tech work. With a blend of challenging work, smart coworkers, and the best company culture, Key Tech is the right company for you. | 12/9/2022 |
| 5630 | Key Tech Baltimore, MD Computer Engineer - Firmware/Software (Full-Time & Intern Positions) Computer Engineering or Computer Science degree Exp: up to 5 years |
Key Tech is hiring computer engineers who crave doing fun and challenging custom embedded systems design. As a computer engineer at Key Tech, you'll create firmware and software that interacts with the real world. Develop embedded algorithms that drive motors, move mechanisms, measure optical signals and communicate with PC software. Help pick processors and design embedded architectures that will be in the next generation of medical devices. Test your code on custom Key Tech designed boards - see your software in action. Interested in designing a complex code base to control microfluidic flow? Want to be challenged with designing a thermal control system which simultaneously measures optical signals? Intrigued by creating code that controls a pneumatic system for DNA analysis? | 12/9/2022 |
| 5631 | Khloris Biosciences Mountain View, CA Cell Therapy Manufacturing Technician B.S. degree in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience. Exp: 0-5 years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated cell therapy manufacturing technician to join our team. The selected candidate will work closely with lead manufacturing technicians, scientists, participate in project and team meeting, and work in a multidisciplinary environment. The duties of this position will involve supporting a multidisciplinary manufacturing team in developing Khloris cell therapy platforms. The ideal candidate will have hands-on expertise and comprehensive understanding of cell therapy manufacturing processes | 12/9/2022 |
| 5632 | Lannett Seymour, IN Product Chemist I BS Degree in Chemistry or related field Exp: 0+ years |
This position is primarily responsible for the laboratory testing of in-process, release and stability samples for commercial drug products. | 12/9/2022 |
| 5633 | Lantheus Medical Imaging Billerica, MA Research Scientist I BS/BA/MS in Chemistry, Pharmaceutics, Engineering or equivalent. Exp: MS: 1-2 years |
Radiochemist/Chemist to conduct radiolabeling studies to support R&D portfolio of new and existing products. Requirements include technical expertise in optimization and troubleshooting of synthesis processes, interaction with and transfer of radiolabeling methodology to contract manufacturing sites, and competency in use of HPLC, UV, radio-detection, LCMS and iTLC methodology. Handling of positron and gamma radionuclides for small scale radiolabeling experiments and analytical analysis of both research and commercial products is required. Communication with contract research organizations required for external studies using R&D test compounds. Data interpretation, issue resolution as needed and final report writing is also required. | 12/9/2022 |
| 5634 | Loop Genomics San Diego, CA Research Associate, System Integration BS degree in chemistry, physics, molecular biology, bioengineering or similar field Exp: 1+ years |
The ideal candidate is a generalist at-heart and be comfortable learning and working in diverse disciplines including hardware, software, molecular biology and biochemistry. Your efforts will significantly contribute to a suite of products and improvements that will help shape the future of biology and change how we evaluate and measure both health and disease. | 12/9/2022 |
| 5635 | Loop Genomics San Diego, CA Research Associate I, Biochemistry, Enzymes & Reagents B.S. degree in biology, molecular or cell biology, biochemistry, biological physics, bioengineering, chemical engineering, or equivalent field of stud Exp: 0-2+ years |
The Reagent Development group is seeking a Research Associate to assist with ongoing preparation of product for market and R&D of new sequencing biochemistry. In this position, candidates will carry out assays to assist in better understanding our reagents to improve the data quality and customer experience. Candidates are expected to be familiar with common laboratory techniques and be eager to learn under the direction of scientists. With mentoring, candidates will be able to develop and optimize methods and techniques for the testing and evaluation of cutting-edge sequencing reagents. | 12/9/2022 |
| 5636 | Loxo Oncology Louisville, CO Research Associate/Associate Scientist, Biophysics BS or MS Exp: 0-3+ years |
The ideal candidate is self-motivated, responsible, and a productive scientist who enjoys collaborating with biologists, chemists, and assay scientists. In this role, he/she will utilize a variety of assay technologies including mass spectrometry, fluorescence spectroscopy, surface plasmon resonance, and isothermal titration calorimetry to evaluate protein/ligand interactions. Experience in protein purification and characterization is a plus. This position requires excellent people skills, a positive can-do attitude, passion for lab work, attention to detail, and the ability to thrive in a highly interactive, fast-paced, team environment. | 12/9/2022 |
| 5637 | Loxo Oncology South San Francisco, CA Research Associate, Proteomics BA/BS, MS in Chemistry, Biology, Biochemistry, or related field Exp: 0-3+ years |
This position is an opportunity to learn and grow within a dynamic discovery biology team dedicated to creating specific targeted therapeutics for genetically defined oncology targets. The ideal candidate is someone who enjoys technical challenges, has the protein handling and cell culture skills needed to drive basic oncology research forward, and will excel in a collaborative environment. Experience with cell culture and biochemical techniques will be critical. Direct experience with sample preparation and method development for mass spectrometry are desirable. The ideal candidate will be enthusiastic about cancer research and is not afraid to get their hands dirty by helping with core lab functions including cell culture, protein characterization, mass spectrometry, and laboratory automation. The qualified candidate will have experience with basic chemistry/biology laboratory practices and is passionate to learn additional techniques working in a growing and dynamic group focused on discovery research. The candidate will work as part of a collaborative team of scientists with expertise in protein characterization, cell culture, chemistry, biochemistry, structure, and biophysics, supporting hit-to-lead and lead-ID phases of our oncology drug programs. The candidate will have opportunities to learn cutting edge techniques and to learn and develop technical expertise in proteomics. | 12/9/2022 |
| 5638 | Lonza Portsmouth, NH Quality Control Analyst, Microbiology BS, AA in Microbiology, Biochemistry or Related Science Exp: 0 yrs |
The QC Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. The QC Microbiology Analyst should be able to provide on-time, high quality results to meet Manufacturing demands. *Shift : Weds-Sat 8PM-6:30AM* *Training will be conducted during the day shift for a few weeks *While working 3rd shift, the employee will receive a 20% shift differential *While working on any Saturday or Sunday, this employee will receive an additional 5% shift differential | 11/28/2022 |
| 5639 | Lonza Portsmouth, NH Quality Control Analyst, Environmental Monitoring Nights BS, AA in Microbiology, Biochemistry or Related Science Exp: 0 yrs |
As our QC Environmental Monitoring Analyst, you will support routine environmental monitoring of air, surface and clean utilities for manufacturing of in process and final product drug lots for customers. This position has a rotating 2-3-2 NIGHTS schedule (on 2 days, off 2 days, on 3 days) 7PM-7AM; While working this shift, the employee will receive a 20% shift differential; While working on any Saturday or Sunday, this employee will receive an additional 5% shift differential | 11/28/2022 |
| 5640 | Culture Biosciences South San Francisco, CA Bioprocessing Associate, Cell Culture Bachelor’s degree in Biology, Microbiology, Chemical Engineering, Biotechnology or a science related background. Exp: 1-2 years |
We are looking for a Bioprocess Associate with a cell culture background to help run our cloud biomanufacturing facility. Your work will contribute to getting novel biotechnology products to market faster and more efficiently. Your job will be to work as part of a team of bioprocess associates, engineers and project leads to execute key customer projects. In particular, you will learn mammalian cell culture techniques and work with state-of-the-art robotics, software, and automation equipment. | 11/28/2022 |
| 5641 | Cyprotex Watertown, MA Research Assistant BS/ MS in a relevant bio scientific discipline Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays | 11/28/2022 |
| 5642 | Cytovance Biologics Oklahoma City, OK QA Operations Associate I Bachelor’s Degree with emphasis on physical or life sciences Exp: 0 to 2 years |
QA Operations Associate I is responsible for maintaining quality oversight of operational areas by working closely with Operation’s personnel and performing various checks during manufacturing processes to ensure that current Good Manufacturing Practices (cGMP’s) are followed. The QA Operations Associate I also assess regulatory and quality risks in activities and processes according to GMP and Cytovance Standard Operating Procedures. | 11/28/2022 |
| 5643 | Day Zero Diagnostics Boston, MA Laboratory Technician Bachelor's degree in a chemical, physical, biological, or clinical laboratory science from an accredited institution, or a medical or biotechnology d Exp: 1 year |
Perform and assist with sample processing toward diagnostic workflows Execute repetitive workflows and strictly follow lab SOPs for specimen handling, processing, and reporting Ensure quality control of clinical samples and able to identify problems that may adversely affect test performance or test result reporting and notifying the appropriate supervisor Maintain meticulous documentation on sample processing and tracking, QC checkpoints, and any corrective actions taken when tests deviate from the laboratory’s established specifications | 11/28/2022 |
| 5644 | Exponential Business & Technologies Eden Prairie, MN Nano Analytical and Testing Lab Technician BE or BS degree in Materials Science and Engineering, Mechanical Engineering, Physics, Chemistry or related disciplines Exp: One to two years |
Ebatco is seeking an energetic, self-disciplined, customer service oriented technical person to join its Nano Analytical and Testing Laboratory (NAT Lab). As a technical member of the NAT Lab team, the technician performs contract lab services and instrument demonstrations with appropriate levels of support and supervision, operates advanced nano/micro scale scientific instruments, collects testing and measurement data, and writes technical report on experimental results and observations. | 11/28/2022 |
| 5645 | Editas Medicine Cambridge, MA Research Associate, In Vivo Pharmacology & Toxicology - 2168 BS/MS biology or related field Exp: 0-2 or 2+ years |
The In Vivo Gene Editing Department at Editas Medicine is looking to add a talented Research Associate to the Pharmacology & Toxicology group. This person will support routine in vivo research studies. The ideal candidate will have the ability to design and execute in vivo experiments using molecular based assays and have experience with various analytical testing methods (ddPCR, qPCR, ELISA, etc.). This individual will get to play a key role in advancing the next generation of pipeline programs at Editas. | 11/28/2022 |
| 5646 | Elektrofi Boston, MA Associate Scientist BS in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biology, Bioengineering, or a related field Exp: 0-2 years |
Elektrofi is looking for an Associate Scientist to support a team responsible for the development of platform formulations for Elektrofi’s proprietary microparticle production process. The candidate will support ongoing activities towards the development of Elektrofi’s biologics formulation platform. This individual will join an early-stage, multidisciplinary team of scientists and contribute to a variety of formulations activities in a highly collaborative environment. | 11/28/2022 |
| 5647 | Elektrofi Boston, MA Engineer I/II B.S. in Mechanical, Chemical, Biomedical, or Materials Engineering, Chemistry, Physics, or a related engineering discipline Exp: up to 2 years’ |
Elektrofi is looking for an Engineer I/II to support manufacturing, process development, or drug product development in the manufacturing and analysis of biologically active microparticle suspensions and their interactions with delivery devices. This individual will join a growing, multidisciplinary team of scientists and engineers and contribute to a variety of manufacturing and process development activities in a highly collaborative environment. | 11/28/2022 |
| 5648 | Elektrofi Boston, MA QC Analyst B.S. in Chemistry, Pharmaceutical Sci. or other relevant discipline Exp: entry-level |
Elektrofi is looking for an QC Analyst to join a team responsible for the qualification, validation and execution of method standard operating procedures (SOPs) to analyze biologically active microparticles. The successful candidate will perform routine testing panels for materials, intermediates, and test articles to support pre-clinical studies. This individual will join an early-stage, multidisciplinary team of scientists and engineers and contribute to a variety of CMC activities in a highly collaborative environment. | 11/28/2022 |
| 5649 | Element Biosciences San Diego, CA Research Associate, System Integration BS degree in chemistry, physics, molecular biology, bioengineering or similar field Exp: 1+ years |
This role will be responsible for key integration activities including running experiments cross-functionally, designing and executing component- and system-level tests and simplifying product workflows. While supported by teams of experts, the ideal candidate is a generalist at-heart and be comfortable learning and working in diverse disciplines including hardware, software, molecular biology and biochemistry. Your efforts will significantly contribute to a suite of products and improvements that will help shape the future of biology and change how we evaluate and measure both health and disease. | 11/28/2022 |
| 5650 | Element Biosciences San Diego, CA Research Associate I, Biochemistry, Enzymes & Reagents B.S. degree in biology, molecular or cell biology, biochemistry, biological physics, bioengineering, chemical engineering, or equivalent field of stud Exp: 0-2+ years |
The Reagent Development group is seeking a Research Associate to assist with ongoing preparation of product for market and R&D of new sequencing biochemistry. In this position, candidates will carry out assays to assist in better understanding our reagents to improve the data quality and customer experience. Candidates are expected to be familiar with common laboratory techniques and be eager to learn under the direction of scientists. With mentoring, candidates will be able to develop and optimize methods and techniques for the testing and evaluation of cutting-edge sequencing reagents. | 11/28/2022 |
| 5651 | EMD Serono St Louis, MO Associate Scientist - Quality Control Bachelor’s Degree in Chemistry, Biochemistry, Biology, Chemical Engineering, or other Life Science discipline Exp: 0+ years |
The Associate Scientist will evaluate assay products according to established protocols and contribute to the support functions to maintain group and department operations. The primary focus of this role is delivery of final assay results. | 11/29/2022 |
| 5652 | EMD Serono Carlsbad, CA Manufacturing Technician II- Cleanroom Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other life science field Exp: 1+ years |
We are offering a $5,000 sign-on bonus for those that qualify. The Manufacturing Technician II position will work in a cleanroom environment and will follow cGMP batch records and SOPs to manufacture viral vector products (including cGMP biopharmaceutical cell culture, buffer and medium preparation, membrane clarification, membrane concentration, and buffer exchange, column purification, terminal filtration, Fill and Finish, stocking supplies and raw materials, and cleaning process equipment). Employees will support projects in conjunction with other GMP Manufacturing personnel (Leads, Supervisors, Managers). Employees will prepare suites for manufacturing, to document deviations, and to operate in a safe and compliant manner. The employee will be self-motivated, work well in a group, and communicate well with all levels of the operations team. | 11/29/2022 |
| 5653 | EMD Serono St Louis, MO Quality Assurance Associate Bachelor’s degree in Chemistry, Biology, or other Life Science field Exp: 0+ years |
At MilliporeSigma, the Quality Assurance Associate provides compliance oversight across the MilliporeSigma Quality Management System (QMS) in collaboration with site personnel. As a QA Specialist you are responsible for the implementation and maintenance of Quality Systems and processes to ensure internal and external compliance and the promotion of quality practices that meet or exceed required guidelines and regulatory requirements. Responsibilities include maintenance and continuous improvement of the overall Quality Program. | 11/29/2022 |
| 5654 | EMD Serono Tamaqua, PA CHE Engineer - ELDP Bachelor’s degree in Chemical Engineering Exp: 1+ years |
The Engineering Leadership Development Program (ELDP) provides a unique opportunity for highly talented and motivated recent graduates to gain valuable experience and training in the multifaceted disciplines of Semiconductor Materials operations. You may work in a production facility developing next generation CMP slurries, ultra-thin dielectric and metal film precursors, or formulated cleans and etching products to serve the semiconductor industry. During the program, members will experience three, 12-month rotational assignments, while receiving exposure to the company's core businesses, processes, technologies, and leaders. The rotations will take place in diverse functions such as Production, Supply Chain, Quality, and Engineering. | 11/29/2022 |
| 5655 | EMD Serono Tamaqua, PA ELE Engineer - ELDP Bachelor’s degree in Electrical Engineering Exp: 1+ years |
The Engineering Leadership Development Program (ELDP) provides a unique opportunity for highly talented and motivated recent graduates to gain valuable experience and training in the multifaceted disciplines of Semiconductor Materials operations. You may work in a production facility developing next generation CMP slurries, ultra-thin dielectric and metal film precursors, or formulated cleans and etching products to serve the semiconductor industry. During the program, members will experience three, 12-month rotational assignments, while receiving exposure to the company's core businesses, processes, technologies, and leaders. The rotations will take place in diverse functions such as Production, Supply Chain, Quality, and Engineering. | 11/29/2022 |
| 5656 | EMD Serono Tempe, AZ Analytical Chemist Master’s degree in Chemistry, Biochemistry, or other Scientific discipline Exp: 1+ years’ |
EMD Electronics in Tempe, AZ is seeking an Analytical Chemist to perform laboratory operations including chemical and physical analysis. | 11/29/2022 |
| 5657 | Millipore Tamaqua, PA MeE Engineer ELDP Bachelor’s degree in Mechanical Engineering Exp: 1+ years |
The Engineering Leadership Development Program (ELDP) provides a unique opportunity for highly talented and motivated recent graduates to gain valuable experience and training in the multifaceted disciplines of Semiconductor Materials operations. You may work in a production facility developing next generation CMP slurries, ultra-thin dielectric and metal film precursors, or formulated cleans and etching products to serve the semiconductor industry. During the program, members will experience three, 12-month rotational assignments, while receiving exposure to the company's core businesses, processes, technologies, and leaders. The rotations will take place in diverse functions such as Production, Supply Chain, Quality, and Engineering. | 11/29/2022 |
| 5658 | Millipore St Louis, MO Scientist, Molecular Biology And Microbiology Bachelor's degree in a Life Science Exp: 1+ year(s) |
The role is responsible for supporting the Technical Leader, as an extended project team member, supporting product development and improvement projects, customer applications, as well as R&D and Marketing activities. | 11/29/2022 |
| 5659 | Millipore Carlsbad, CA Specialist II, Analytical Development Master’s Degree in chemistry, Biochemistry, Biology, or similar life science discipline Exp: 1+ years |
MilliporeSigma is seeking a motivated Specialist II- Analytical Development to join its dynamic and collaborative process development team at the Carlsbad viral vector CDMO facility. The successful candidate will play a key role in developing analytical methods to support viral vector process development activities, including method qualification and validation activities. The candidate will also act as a driver for continuous advancement in viral vector analytical science and operational excellence across functions. | 11/29/2022 |
| 5660 | Millipore Rocklin, CA Histology Lab Manufacturing Technician Bachelors’ Degree in Chemistry, Biology, or other Biological Science discipline. Experience using a microtome. Exp: 1+ years’ |
At MilliporeSigma, the Histology Lab Manufacturing Technician is responsible for performing Histology related functions. This includes microtomy, staining of tissue by immunohistochemistry (IHC), tissue processing and embedding. The ideal candidate has experience using a microtome and is eager to work as a team to meet departmental goals and deadlines. This position reports to the Manufacturing Supervisor as part of the Operations team located at the Rocklin Site, where we manufacture products for use in in vitro diagnostic (IVD) IHC. | 11/29/2022 |
| 5661 | Millipore Allentown, PA Process Engineer MS degree in Chemical Engineering Exp: 0-3 years |
At EMD Electronics, a Process Engineer in the Integrated Supply Chain (ISC) Process Engineering group, you will collaborate with project management and EPC contractors as the responsible engineer for all process design questions. You will also interact very closely with site operations, process safety, and the process development group in the execution of the responsibilities of this position. | 11/29/2022 |
| 5662 | Millipore Milwaukee, WI Associate Production Scientist Bachelors Degree in Chemistry, Biochemistry, Biology, Chemical Engineering, or other Life Science field Exp: 1+ year |
Manufacture, package, and evaluate products according to established protocols, provide technical support to others, lead safety initiatives & projects, and perform operations in support of the group and department. This is a 3rd shift position with regular scheduled work hours of 10:00pm-6:30am Sunday – Friday but may occasionally differ depending on business needs. | 11/29/2022 |
| 5663 | Endo Pharmaceuticals Rochester, MI Process Engineer I BS degree in Engineering or Chemical Engineering OR MS Exp: BS: 0-3+ years’ ; MS: 0-1+ year |
The Process Engineer I, with guidance, performs various duties related to optimization and analysis of production processes, new products, processes and technology transfers. Prepare and execute engineering study protocols, manufacturing and packaging experimental / feasibility study / validation batch records and protocols and complete interim and / or final summary reports for marketed and new products. Perform or assist on-site and site-change technical transfer, scale-up or scale-down factor evaluation, manufacturing / packaging process and equipment troubleshooting, and SOP preparation and review. | 11/30/2022 |
| 5664 | Endo Pharmaceuticals Rochester, MI Associate Process Engineer, Set-up Specialist - Afternoon Shift Bachelor’s Degree or higher in Engineering or Science related equivalent, preferred. Exp: 1-3 years’ |
The Associate Process Engineer, Set-up Specialist, works in a hands-on capacity in a fast-paced, cGMP environment and production support areas to process sterile and aseptic products. The specialist works in collaboration with Operations, Maintenance, Engineering and Validation for successful repeatable day-to-day manufacturing operations. The role operates and supports one or more of these manufacturing departments: Formulation, Filling, Inspection, Packaging. | 11/30/2022 |
| 5665 | Endo Pharmaceuticals Rochester, MI Chemist II (Afternoon Shift) Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years’ |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 11/30/2022 |
| 5666 | Enzo Life Sciences Farmingdale, NY Technologist (Chemistry) Bachelors Degree in Clinical Laboratory Science, Medical Technology or related degree, preferred Exp: one (1) year |
The technologist will perform qualitiative and quantitative tests and examinations using various analyzers and/or manual methods. Assist in performing established quality assurance procedures (quality control testing, instrument function checks and calibrations). Maintains appropriate documentation and reports irregularities. Shift: 10:00PM - 6:30AM (Flexible Hours and receive a sign-on bonus) | 11/30/2022 |
| 5667 | Enzo Life Sciences Farmingdale, NY Technologist (Molecular) Bachelors Degree in Clinical Laboratory Science, Medical Technology or related degree, preferred Exp: one (1) year |
The technologist will perform qualitative and quantitative tests and examinations using various analyzers and/or manual methods. Assist in performing established quality assurance procedures (quality control testing, instrument function checks and calibrations). Maintains appropriate documentation and reports irregularities. Evening Shift: Tues-Sat 3:00pm-11:30pm and alt weekends as needed | 11/30/2022 |
| 5668 | Enzo Life Sciences Farmingdale, NY Associate Scientist Bachelor’s or Master’s Degree in Chemistry or other scientific field. Exp: 1+ years |
Working under the direct supervision of the Director of Chemistry, this position is responsible for the synthesis, purification, and quality control of small molecule compounds and other chemistry products. | 11/30/2022 |
| 5669 | Exelixis Alameda, CA Scientist II - Tumor Biology MS/MA degree in related discipline Exp: one year |
We are looking for a Scientist to join our Tumor Biology group. The successful candidate will have prior experience to evaluate the activity of small molecules in cell-based assays for oncology drug discovery. The successful candidate will also have prior experience with isolation and culture of cancer-associated fibroblasts (CAF) and tumor/stromal cell in vitro co-culture system for modeling the in vivo stromal compartment in the tumor microenvironment. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. | 11/30/2022 |
| 5670 | Exelixis Alameda, CA Scientist III MS/MA degree in related discipline Exp: one year |
We are looking for a Scientist to join our Tumor Biology group. The successful candidate will have prior experience to evaluate the activity of small molecules in cell-based assays for oncology drug discovery. The successful candidate will also have prior experience with isolation and culture of cancer-associated fibroblasts (CAF) and tumor/stromal cell in vitro co-culture system for modeling the in vivo stromal compartment in the tumor microenvironment. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. | 11/30/2022 |
| 5671 | Exelixis Alameda, CA Assoc Scientist Bachelor’s degree in chemistry, biochemistry, pharmaceutical sciences or related field Exp: one year |
The lab operations supervisor will assist the CMC team by managing the daily activities in the lab. The successful candidate will be highly motivated, have strong communication skills, be resourceful and well organized. | 11/30/2022 |
| 5672 | Exelixis Alameda, CA Scientist I (Pharmacology) MS degree in related discipline Exp: zero to two years |
The hands-on Scientist I (Pharmacology) will support the in vivo pharmacology research program and contribute to the multidisciplinary research team by designing and executing in vivo studies for pharmacokinetics and toxicology. The successful candidate will be a highly creative scientist with a strong desire to succeed at the highest level. | 12/1/2022 |
| 5673 | Fresenius Kabi Melrose Park, IL Manufacturing Engineer - Packaging (Fri, Sat, Sun Nights) Bachelor’s degree in Engineering (Electrical, Mechanical, Automation, Controls, Computer, etc.). Exp: 1-3 years |
Manufacturing Engineer - Packaging is responsible for using technical expertise in support of daily operations in packaging operations by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity. Apply accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyze situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 12/1/2022 |
| 5674 | DVC LLC Silver Spring, MD Research Assistant BS in Biology, Microbiology, Medical Technology or related field Exp: 1+ years |
This position would provide support to the NMRC IDD Wound Infections Department by carrying out laboratory research procedures for working with multidrug resistant bacteria causing traumatic wound infections. | 12/1/2022 |
| 5675 | Genentech Seattle, WA Research Associate Doctorate, Master’s or Bachelor’s degree in Molecular biology, Protein Engineering, Bioengineering, Biochemistry or related field Exp: 1 year |
After training on our current work processes and established SOPs, execute defined sequencing experiments that advance research and development efforts on our multifaceted nanopore-based sequencing platform. • Use technical and theoretical understanding to explain experimental findings while keeping experimental protocols and data well organized and documented. • Communicate actively, effectively, and promptly with manager on project status, data analysis findings, experimental observations, and process deviations. • Support management decisions and goals in a positive, professional manner. Embrace priorities and responsibilities set forth by management. • Analyze and interpret experimental data using various data analysis software (e.g., Excel, Python) and/or applying quantitative methods. • Prepare clear data summaries that include conclusions and follow-up steps to review with manager. When needed, effectively present findings to team members. | 12/1/2022 |
| 5676 | Genentech Indianapolis, IN QUALITY CONTROL TECHNICIAN - DIABETES CARE (2ND SHIFT, CONTRACT) Bachelor’s degree in technical or scientific field or equivalent experience Exp: 1+ years’ |
Perform analyses finished product from other sections of manufacturing or performs investigations according to established procedures to determine conformance to acceptance specifications for a particular chemical or physical property. Prepares instruments and apparatus according to established procedures to support the testing activities of the unit. May monitor and verify quality in accordance with statistical process or other control procedures. | 12/1/2022 |
| 5677 | Genentech Hillsboro, OR QUALITY CONTROL TECHNICIAN (CONTRACTOR) B.A. or B.S. degree (preferably in Life Science) Exp: 1-3 years |
Responsibilities include performing and reviewing a variety assays in the Quality Control organization in support of In-Process intermediates, drug substance, drug product and stability sample testing in a cGMP environment. The QC Technician must be able to interpret data troubleshoot assay failures and equipment issues while adhering to strict guidelines on cGMP documentation. In addition, the individual will support cycle development, performance qualifications, method transfers, discrepancy/out of specification investigations and collaborate with external groups to identify improvement opportunities in technology and business process. Shift: Sunday to Wednesday or Wednesday to Saturday, 4x10’s Day: 6:30am to 5:00pm Swing 11:30am to 10:00pm Contract duration: 12 months with possible extension up to 3 years | 12/1/2022 |
| 5678 | Genentech South San Francisco, CA SCIENTIST 2/3, PROCESS DEVELOPMENT AND OPTIMIZATION, SMALL MOLECULE PROCESS CHEMISTRY MS in Chemical Engineering or Chemistry. Exp: 1+ years |
Genentech, a leader in bio-pharmaceutical sciences, is seeking a highly-motivated and talented researcher with a proven track record of laboratory achievements to join our growing Department of Small Molecule Process Chemistry. | 12/1/2022 |
| 5679 | Genentech Hillsboro, OR ENGINEER II/SENIOR ENGINEER, MAINTENANCE B.S or higher in Chemical, Biochemical, Electrical or Mechanical Engineering or related discipline Exp: 1-5+ years |
Collaborate with management to establish priorities, milestones and targets. Represent the department functionally, cross functionally and cross site for various activities and initiatives applying discretion to independently address issues or resolve problems. Facilitate and/or participate in various activities such as gap analysis and root cause analysis. Provide technical support for instrumentation and maintenance related activities associated with manufacturing equipment / systems, Tank Management, and Critical GMP utility systems located at the Genentech Hillsboro Technical Operations fill finish facility. Provide technical writing assistance for Instrumentation and maintenance support documentation and changes. | 12/1/2022 |
| 5680 | BioVision Fremont, CA Research Associate/Sr. Research Associate BS Degree in biochemistry, pathology, cell and molecular biology, immunology or other Life Sciences. Exp: 0-3 years |
Focus on the development and validation of qualified antibodies for IVD immunohistochemistry (IHC) applications under FDA and MDSAP/ISO13485 (2016) quality standards. | 11/21/2022 |
| 5681 | Blueprint Medicines Cambridge, MA Associate Scientist, Biology MS in oncology, cellular biology, molecular biology, or related discipline Exp: 1-3 years |
This position offers the opportunity to impact a growing portfolio of targeted therapies in a fast-paced and innovative research environment. We are searching for a dynamic Associate Biology Scientist with experience interrogating cellular and molecular mechanisms as they relate to kinase target pathway modulation, off-target liabilities, and resistance. | 11/21/2022 |
| 5682 | Cambrex Charles City, IA Chemical Development Scientist I M.S. in Chemistry or related field Exp: no experience |
Position is directed toward optimization of existing chemical routes and development of alternate chemistry toward key synthetic intermediates and APIs. Carries out multistep chemical synthesis and product isolation/purification operations in the laboratory, independently or as part of an integrated team. Chemist utilizes modern analytical tools to determine identity and purity of products made during projects. Communication with clients in regular team meetings; prepares R&D reports at the conclusion of projects. | 11/23/2022 |
| 5683 | Cambrex Agawam, MA QA Specialist I Related BA/BS degree Exp: 0-2+ years |
The QA Specialist I supports the Quality Management System (QMS) and the Document Management System (DMS) in a GMP regulated environment according to established operating procedures. The QMS and DMS functional areas include but are not limited to: Document Control, Training, Deviations, Out of Specification Investigations, Corrective and Preventive Actions (CAPA), Change Control, Complaints, Quality review of analytical and microbiological data and batch production records, Internal Audits, Supplier/Subcontractor Management, Validation, and Calibration & Maintenance. | 11/23/2022 |
| 5684 | Advanced Sterilization Products Skillman, NJ Scientist I, Skin Health R&D PPI Body Master’s degree in Chemistry, Chemical Engineering, Industrial Pharmacy, material science or other science or engineering discipline is preferred. Exp: 0-1 years |
The Scientist will support the product development of regional and global projects for new Body Moisturizers and Cleansers. He or she will work closely with their manger and team to understand how to improve and build on our Body pipeline initiatives. They will also partner closely with all functions responsible for launching a product to help assess risk, understand, and proactively solve for potential hurdles to ensure successful new product launches. Responsibilities and primary duties include formulation prototype development and batching, including stability and consumer evaluation, attending project update meetings and project related documentation. Excellent communication skills together with the ability to manage complexity are must-have prerequisites. | 11/24/2022 |
| 5685 | Advanced Sterilization Products Brisbane, CA Associate Scientist, in Vitro Assays Gene Therapy Discovery M.S. Exp: 1 year |
We are seeking a highly motivated and independent Associate Scientist to join a group that is developing in vitro assays to characterize the functional activity and potency of therapeutic proteins delivered via adeno-associated virus (AAV) or other viral vectors to HEK293 cells and disease cell models. The qualified scientist should have experience working in the field of gene therapy and technical expertise with in vitro functional assays and mammalian cell culture, AAV transduction, and in vitro functional assays. The scientist will plan and execute experiments, follow protocols, interpret data, troubleshoot problems, document data, and communicate results, while working in a collaborative environment that values innovation, leadership, scientific excellence, and personal accountability. | 11/24/2022 |
| 5686 | Advanced Sterilization Products Skillman, NJ Assistant Scientist, Skin Health & Beauty Bachelor’s degree Exp: 1-3 years |
The R&D Skin Health and Beauty Assistant Scientist will lead new product launches and life cycle management for Skin Health and Beauty products, with a focus on the Facial Moisture category. This person will be expected to develop and demonstrate expertise in product and process development. Working cross-functionally, they will be a key member working end-to-end to launch a product and maintain it through its life cycle. Responsibilities and primary duties include formulation prototype development, product robustness and consumer evaluation, attending project meetings, and creation of supporting documentation. Excellent interpersonal skills together with the ability to handle complexity are must-have prerequisites. | 11/24/2022 |
| 5687 | Catalent Baltimore, MD Associate Scientist III M.S. in Chemical Engineering, Chemistry, Biochemistry, Life Sciences Exp: 1-3 years |
The Associate Scientist III functions independently and is actively engaged in process and product development within a dynamic project team with supervision. Displays strong technical knowledge, initiative and scientific commitment, and makes significant scientific and technical contributions to downstream process development within the Pre-Clinical Downstream Development Group. Work Schedule: 9am-5pm or 10am-6pm | 11/24/2022 |
| 5688 | Catalent Chelsea, MA Quality Control Analyst - Microbiology Bachelor’s?Degree?in life sciences or a related field?required.? Exp: 1 year |
Catalent Pharma Solutions is Chelsea, MA is hiring a Quality Control Analyst, Microbiology who is responsible for Environmental Monitoring sampling, analyzing, and microbiological testing to support GMP manufacturing. They will conduct routine and non-routine environmental and utilities monitoring and perform microbial testing of samples according to standard operating procedures. The Quality Control Analyst compiles data for documentation of test procedures, participates in the preparation of investigations, summaries and reports, and reviews data obtained for compliance to specifications and reports out-of-trend and/or out-of-specification results. | 11/24/2022 |
| 5689 | Catalent Morrisville, NC Associate Scientist - CONVERSION Bachelor’s Degree in chemistry or closely related physical science Exp: 1-3 years |
Execute laboratory work plan/schedule developed with input from supervisor or senior team member May draft technical documents such as methods or certificates of analysis Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance Trains others on laboratory techniques Assists in the execution of efficiency improvement project with guidance | 11/24/2022 |
| 5690 | Catalent Morrisville, NC Scientist Master’s degree Exp: 1-2 years |
Execute laboratory workplan/schedule developed with input from supervisor or senior team member May draft technical documents such as methods or certificates of analysis Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness, and regulatory compliance Trains others on procedures and laboratory techniques Executes efficiency improvement project with guidance | 11/24/2022 |
| 5691 | Catalent Baltimore, MD Associate Scientist III M.S. in Molecular Biology, Chemistry, Biology, Life Sciences, or related field Exp: 1-3 years |
Catalent Cell and Gene Therapy is looking to recruit an Associate Scientist III to join our growing team in Baltimore, MD. The Associate Scientist III functions independently and productively as an Analytical Scientist and is actively engaged in the process and product development within a dynamic project team. Displays strong technical knowledge, initiative, and scientific commitment, and makes significant scientific and technical contributions within the Process Development Group. Serves as a technical lead and interacts with clients and Supervisors to ensure project goals are met. | 11/24/2022 |
| 5692 | Catalent Kansas City, MO Associate Scientist II - Bio Separations Bachelor's degree in life sciences such as chemistry, biochemistry, biology or closely related physical science required Exp: 0-3+ years |
Catalent Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II for our Biologics II Team. The main activities will be to provide and report data, as required by project contracts within the Biologics Department. The data may be used for submission in Regulatory packages, release and stability testing of clinical and animal trial dose forms and in support of development projects. This is a full-time role position: Monday – Friday, days.\ | 11/24/2022 |
| 5693 | Cayman Chemical Ann Arbor, MI Associate Scientist I - ELISA R&D Master's degree in Life Sciences or Chemistry preferred Exp: 1-year |
Assist in development of new ELISA’s, including but not limited to: immunogen and tracer development, antibody/antisera characterizations, formulation and stability testing, sample analysis, and validations Help prepare and maintain Laboratory SOPs and product inserts General upkeep of the lab and maintenance of laboratory equipment and raw materials inventory Keep complete, current, and accurate records of all experiments, techniques, procedures, and results in a laboratory notebook Reads scientific literature with accuracy and understanding; keywords articles as needed Utilize resources including but not limited to EndNote, PubMed, and journal articles Reports status of work to supervisor regularly, i.e. weekly updates, monthly report, etc. Present project updates at group and departmental meetings | 11/24/2022 |
| 5694 | Celldex Therapeutics Hampton, NJ Assistant Scientist BS/BA degree or Associates Degree with experience in related field. Exp: 0-2+ years |
The Assistant Scientist provides daily care of research animals for experimental purposes, including performing basic husbandry duties. Responsible for maintenance of the Animal Facility including regular facility sanitation. Performs in vivo research support duties such as sample collection, data collection, treatment dosing, and can develop new skills as required based on research needs. In addition, the Assistant Scientist will be responsible for planning their schedule to assist with in vitro assays and cell culture. | 11/24/2022 |
| 5695 | Cerus Concord, CA Engineer I or II (hybrid) Master’s degree in chemical, mechanical, or biomedical engineering Exp: 0-2+ years |
Provide laboratory and engineering support for the Class III INTERCEPT Blood System for Platelets and Plasma. Focused primarily on new product development, manufacturing product and quality improvements, supply chain assurance, and margin expansion projects. Includes laboratory testing of and for single-use INTERCEPT Processing Sets and components thereof. | 11/25/2022 |
| 5696 | Champion Oncology Rockville, MD Research Technician II, Study Services BS/MS degree in biology, pharmacology, or related field Exp: 1 year |
As a Research Technician in Study Services, you will support in vivo oncology studies in mice. Additional duties and responsibilities include: Perform in-life technical procedures, handle, restrain, and provide care for all animals; Observe animals for general health and overall well-being Administer therapeutic agents by various routes; Provide animal welfare assessments, including body weight and tumor volume measurement Allocate animals to study and non-study groups; Provide preoperative animal care; Euthanize animals as directed in study protocols and directives; Read study protocols and extract pertinent information; Perform study preparation activities including collection tube labeling and room/BSC set-up Record data using laboratory information management systems; Work weekends and holidays on rotating basis | 11/25/2022 |
| 5697 | ChemGenes Wilmington, MA Senior Research Support Associate B.S. degree in Biochemistry, Biology or related field Exp: 0–2 years |
Manufacture of synthetic DNA & RNA compounds. Assist with experiments supporting research in the synthesis of single-cell-barcoded beads, quality control of the synthesized beads, and performing experiments that include basic molecular biology techniques to sequencing experiments to validate and troubleshoot synthesis of DNA oligos to beads. Provide comprehensive technical support for scientists in the company; executing and optimizing ongoing experiments, analyzing results and designing follow-up experiments based on the results, and presenting findings and insights at group meetings. Evaluating research methods, procedures and techniques based on established objectives, conceiving and designing basic experimental protocols to ensure project completion in a timely fashion; recording and organizing data generated from the experiments in clear, concise, and assessable format; perform basic coding and statistical analyses; processing of in-vitro and in-vivo RNA for preparation of RNA-seq libraries for sequencing in Illumina platforms (Mi-Seq including Hi-seq and Next-seq). Experienced in techniques including but not limited to: running agarose gel, polyacrylamide gel electrophoresis, reverse transcription, quantitative PCR, fluorescent microscopy, flow cytometry; maintaining inventories of lab stocks. | 11/25/2022 |
| 5698 | Cognate BioServices S. San Francisco, CA Research Associate I BS in the biological sciences or relevant area required. Exp: 0-3 years |
Explora BioLabs, an entity of Charles River, is seeking a Research Associate I located in San Francisco, CA. In this role, the incumbent will perform a variety of animal procedures to support company and client research projects (e.g., set up the study forms, set up the procedure rooms, label and ship samples, etc.). To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions | 11/25/2022 |
| 5699 | Cognate BioServices Mattawan, MI Research Analyst I - Formulations Bachelor’s/Master’s degree in a relevant field Exp: no experience |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. *Training will be performed Mon - Friday 6:00 AM - 2:30 PM. Following the completion of training standard working hours will be Friday - Monday beginning at 6:00 AM. Depending on assigned shift, additional hours could be required or requested during nights, weekdays, weekends and/or holidays. | 11/25/2022 |
| 5700 | Cognate BioServices Mattawan, MI Research Technician - Surgery and Efficacy - Surgery OR HS/GED/Bachelor's degree (preferred, not required) Exp: no experience |
Job Summary **$1,000 Sign-On Bonus*** **1st Shift Mon-Fri 700am-330pm** We are seeking an experienced Research Technician for our Surgery (OR) Team at our Safety Assessment site located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.Job Summary | 11/25/2022 |
| 5701 | Cognate BioServices Boston, MA Surgical/Research Veterinary Technician - Position includes a $2,000 sign on bonus Bachelor’s degree (B.A./B.S.) or equivalent in animal science preferred. Exp: (6) months |
Help us contribute to beating pediatric cancers! Boston Children's Hospital is focusing research on finding cures for pediatric cancer and Charles River is looking for talented, caring and committed surgical veterinary technician to contribute to these life-saving efforts. | 11/25/2022 |
| 5702 | Cognate BioServices Mattawan, MI Research Analyst I - Formulations Bachelor’s/Master’s degree in a relevant field Exp: no experience |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. *Training will be performed Mon - Friday 6:00 AM - 2:30 PM. Following the completion of training standard working hours will be Friday - Monday beginning at 6:00 AM. Depending on assigned shift, additional hours could be required or requested during nights, weekdays, weekends and/or holidays. | 11/25/2022 |
| 5703 | Cognate BioServices Reno, NV Research Analyst I -Bio/Immunology 1 Bachelor’s degree (B.A. / B.S.) in biological science or related discipline preferred. Exp: 6 Months |
We are seeking a Research Assistant 1 for our Safety Assessment site located in Reno, NV. This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 11/25/2022 |
| 5704 | Companion Medical North Haven, CT Chemist I Bachelor’s degree in chemistry, biology, material science, or related technical discipline Exp: 0 years |
The chemist will be responsible for performing Non-volatile Residue (NVR) analysis, extractions and sample preparations in an analytical chemistry lab. The position has responsibility for executing chemical characterization test methods and protocols, including sample preparation, extraction studies and instrumentation setup. The role functions as part of an analytical chemistry team that works under ISO17025 and ISO 13485 requirements in the medical device field. | 11/25/2022 |
| 5705 | Companion Medical Santa Ana, CA Microbiologist-Sterilization I - Santa Ana, CA Bachelor's degree in science or a technical discipline Exp: 0 years |
In this exciting role as a Microbiologist-Sterilization I you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 11/25/2022 |
| 5706 | Companion Medical Santa Rosa, CA Microbiologist-Steriliz I Bachelors degree required Exp: 0 years |
Responsibilities may include the following and other duties may be assigned. Analyzes chemical, biological or microbiological products, raw materials, in-process materials, release test samples or stability samples in support of the company's quality program. Prepares, cleans, disinfects, and/or sterilizes instruments, materials, products, and/or supplies. Follows protocols and regulations in order to clean, store, and/or deliver products, supplies, and/or instruments. Interprets and evaluates the analyses in terms of accuracy and precision compared against established specifications and recommends and implements corrective action where necessary. | 11/25/2022 |
| 5707 | Companion Medical Santa Ana, CA Microbiologist II Master's degree (Advanced) Exp: 0 years |
In this exciting role as a Microbiologist-Sterilization II you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 11/25/2022 |
| 5708 | Companion Medical Rice Creek, MN Chemist II Advanced Degree in Chemistry or a related technical discipline Exp: 0+ years |
As a Chemist II, you will focus on supporting the Analytical Development initiatives to support new and existing technologies. This role requires effective collaboration, time management and prioritization of multiple concurrent tasks in a team focused environment. | 11/25/2022 |
| 5709 | Companion Medical Irvine, CA Microbiologist-Sterilization II - Irvine, CA Advanced degree in science or technical field Exp: 0+ years |
In this exciting role as a Microbiologist-Sterilization II you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 11/25/2022 |
| 5710 | CooperSurgical Palo Alto/Los Altos, CA Laboratory Technician Bachelor's degree in Science preferred Exp: One to two years |
Position Summary: Performs routine semen banking procedures | 11/25/2022 |
| 5711 | CooperSurgical Livingston, NJ Laboratory Technician I Bachelor’s or Master’s Degree in Biology or other related science Exp: 1 year |
Position Summary: Performs complex molecular-based procedures on clinical samples. Analyzes clinical results and provides diagnoses. Performs clinical tasks associated with clinical cases | 11/25/2022 |
| 5712 | CooperSurgical Livingston, NJ Lab Technician I Bachelor's degree in the sciences OR a Master's degree in Biology or related science Exp: one year |
Position Summary: Performs complex molecular-based procedures on clinical samples. Analyzes clinical results and provides diagnoses. Performs clinical tasks associated with clinical cases. | 11/25/2022 |
| 5713 | CooperSurgical Livingston, NJ PGT-M Labratory Technologist Bachelor’s or master’s degree in Biology or other related science Exp: 1 year |
The PGT-M Laboratory Technologist performs complex molecular-based procedures on clinical samples. Analyzes clinical results and provides diagnoses. Performs clinical tasks associated with clinical cases. | 11/25/2022 |
| 5714 | CooperSurgical Los Angeles, CA Laboratory Technician I Bachelor's degree in Science preferred Exp: one to two years |
Position Summary: Performs routine semen banking procedures | 11/25/2022 |
| 5715 | CooperSurgical Cambridge, MA Laboratory Technician I Bachelor's degree in Science preferred Exp: one to two years |
Position Summary: Performs routine semen banking procedures | 11/25/2022 |
| 5716 | Contract Pharmacal Hauppauge, NY Chemist (Quality Control) Bachelor’s degree in Chemistry or related science required Exp: 1 to 9 years |
The Chemist, QC position is responsible for and has experience in performing chemical testing and completion of real-time documentation per cGMPs and current SOPs. | 11/25/2022 |
| 5717 | Crown Bioscience San Diego, CA Research Associate I - Biomarker & Diagnostic Tech Bachelor of Science degree or above in biotechnology, cell biology, immunology, oncology or other related disciplines Exp: one year |
The purpose of the Research Associate I position is to provide support on biomarker discovery studies to meet company's goals, objectives and quality standards. | 11/25/2022 |
| 5718 | Crown Bioscience San Diego, CA Research Associate I - Inflammation & Immunology Associate's degree or Bachelor's degree in Biology, Biotechnology or other relevant area of scientific discipline. Master's degree in biology in Biol Exp: 1-2 year(s) |
The purpose of the Inflammation and Immunology Research Associate I position is to perform primarily in vivo animal studies within the Inflammation and Immunology group in support of the Company's goals and objectives. | 11/25/2022 |
| 5719 | Crown Bioscience San Diego, CA Research Associate I, In Vivo Oncology Bachelor’s Degree in a scientific discipline Exp: One year |
In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 11/25/2022 |
| 5720 | Avantor Sciences Bridgewater, NJ Associate Scientist - Downstream MS degree in biochemistry, molecular biology, chemistry, cell biology, chemical engineering, or bioengineering Exp: 6 + months |
The Associate Scientist - Downstream will be responsible for the hands-on execution of laboratory experiments for the protein purification process and contribute to the development and optimization of processes. The primary responsibilities will include: • Executing and supporting downstream purification (e.g., monoclonal antibodies, fusion proteins, etc.) on a bench-scale jointly with other scientists or independently. • Conducting pilot-scale material generations with the team. • Preparing and executing experimental protocols and analytical test methods under general guidance. • Accurately documenting all procedures and observations • Maintaining laboratory area, utilizes safe practices while working in the laboratory environment as per EHS guidelines and policy. | 11/14/2022 |
| 5721 | Bardy Diagnostics Cleveland, MS Process Engineer I Bachelor Degree in Engineering Required (Mechanical, Industrial, Electrical, or Computer degrees are preferred) Exp: 1 or more years |
This position is a key role in the Injection Molding and Devices. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Injection Molding and Device Operations. Cross-functional project management will be involved in this role as well. | 11/14/2022 |
| 5722 | Bardy Diagnostics Skaneateles Falls, NY Electrical Engineer I Bachelor of Science degree in engineering. Exp: 1+ years |
You are a problem solver. Complex projects or unexpected challenges are just opportunities to bring your considerable abilities to use. Whether working independently or with a trusted team, you are always ready to tackle a project and work hard to find solutions. The Electrical Engineer, Sustaining will be responsible for the design, design verification, and design documentation for our Front Line Care business unit. | 11/14/2022 |
| 5723 | BASi Research Products Rockville, MD Associate Scientist I (In Vitro Cytogenetics) Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 1+ years |
Position Responsibilities: Perform a wide variety of in vitro assays or tests required to characterize product or material safety Maintain sterile and good cell/tissue culture techniques Prepare study reagents in accordance with SOPs and study instructions Use and maintain scientific equipment, instrumentation and computer systems Conduct pre-designed assays using basic laboratory techniques and skills Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations | 11/14/2022 |
| 5724 | BASi Research Products Raleigh, NC Research Associate I B.S. degree Exp: > 0-1 year |
Join us in embracing research and science to impact the health and well-being of people all over the world. Inotiv is expanding our In Vivo Toxicology team. We are a contract research organization performing regulated toxicology studies in laboratory rodents for commercial and governmental clients. J | 11/14/2022 |
| 5725 | BASi Research Products Rockville, MD Associate Scientist II (Secondary Assays) Master’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 0+ years |
Position Responsibilities: Perform a wide variety of in vitro or in vivo Comet assays or tests required to characterize a product or material safety Maintain sterile and good cell/tissue culture techniques Prepare study reagents in accordance with SOPs and study instructions Use and maintain scientific equipment, instrumentation and computer Conduct pre-designed or custom assays using laboratory techniques and skills Perform in vivo Comet tasks such as: necropsy, tissue collection, tissue processing slide preparation and electrophoresis Make scientific observations, maintain detailed data books/documentation, and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations Analyze data and interpret results with input from senior staff, as needed Ensure all testing guidelines are followed for assays performed | 11/14/2022 |
| 5726 | BASi Research Products West Lafayette, IN Bio Analyst I B.S. in chemistry or biology Exp: one year |
Position Summary Conducts sample analysis with data interpretation and basic troubleshooting. Conducts method development and method validation experiments. Assists with general housekeeping and assist other departmental personnel as necessary. | 11/14/2022 |
| 5727 | BASi Research Products Raleigh, NC Research Assistant A.S. or B.S. in biology or related field Exp: 0-3 years |
The Genetic Toxicology Group conducts standard and custom genetic toxicology testing and applied research supporting preclinical studies for both federal and commercial clients. | 11/14/2022 |
| 5728 | Bausch & Lomb Wilmington, MA Quality Engineer I Bachelor of Science, preferably in Engineering, Science (Chemistry, Biology, Physics, etc) or Math (Statistics). Exp: 1-2 years |
Responsible for providing quality engineering and quality management systems support to the Wilmington manufacturing site. | 11/14/2022 |
| 5729 | Bausch & Lomb Rochester, NY Scientist I - Formulations B.S. in chemistry or related biological science discipline will be considered. Exp: 0 to 4 years |
Scientist I position supporting the research, design, and development of lens care products to drive future technologies. A laboratory based position within the R&D Formulation team at the Rochester, NY site. This position will focus on the preparation and characterization of new solution prototypes and marketed product support. | 11/14/2022 |
| 5730 | Bausch Health Bothell, WA Quality Assurance Specialist I (WA) Quality Assurance Specialist I (WA) Quality Assurance Specialist I (WA) 4 years bachelor level degree in Science, engineering or other similar discipline. Exp: 1-3 years |
The Quality Assurance Specialist I will perform complaint investigation activities for product complaints and Adverse Events with cross functional team members and provide complaint investigation reports in compliance with Solta procedures, Food and Drug Administration (FDA), International Standards Organization (ISO), Quality System requirements, and other regulatory guidelines. | 11/14/2022 |
| 5731 | Beckton Dickinson Glens Falls, NY Manufacturing Quality Engineer (onsite) Bachelor’s Degree in Engineering or Technical Sciences. Exp: 1 years |
The Quality Engineer will be responsible for engineering support and direction of QC/QA activities to support design to manufacturing and manufacturing to manufacturing transfers at the GFO site. | 11/14/2022 |
| 5732 | Be Biopharma Kendall Square, MA Process Engineer, B Cell Core BS or MS in Chemical Engineering, Biology, Analytical Chemistry, Biochemistry, Cell & Molecular Biology, or related discipline Exp: 0-2 years |
Be Biopharma is seeking a candidate to help build the B Cell Core Team. Team members will work on early-stage process development and production of novel autologous and allogeneic B cells. There are three major responsibilities within B Cell core- optimize methods for B cell manufacture; deliver B cells for in vivo and developmental studies; and lead documentation for internal and external tech transfer. Roles and responsibilities will be given based on experience and knowledge in the cell therapy field. This is an excellent opportunity for career growth as you would interact with various programs teams and would be involved in regulatory document preparation. | 11/14/2022 |
| 5733 | Be Biopharma Kendall Square, MA Sr./Research Associate, Analytical Development BS or MS in Chemical Engineering, Biology, Analytical Chemistry, Biochemistry, Cell & Molecular Biology, or related discipline Exp: 0-2 years |
Role: Be Biopharma is seeking a Sr. / Research Associate candidate to join the growing Analytical Development (AD) department. AD is responsible for establishing molecular, cell-based, and impurities methods used to characterize B cell drug products as well starting materials (ie AAV vector). The Sr. / Research Associate will be tasked with leading / supporting the different stages of assay development, feasibility, robustness, and prequalification. This is an excellent opportunity for career growth as you would interact with various programs teams and be involved in regulatory document preparation. | 11/15/2022 |
| 5734 | Be Biopharma Kendall Square, MA Sr. Research Associate/Associate Scientist, Cell Engineering BS/MS in Cell and Molecular Biology, Bioengineering, Immunology, Pharmacology or a related field Exp: 1+ years |
Be Biopharma is looking to hire a Senior Research Associate / Associate Scientist to join our Cell Engineering Team and support the genomic safety assessment for our B cell medicines. We are looking for highly motivated, experienced, and innovative thinkers to join our growing team of passionate researchers to leverage B cells as a novel class of cellular medicine. This is an exciting opportunity to be part of a foundational team and help build Be Bio! | 11/15/2022 |
| 5735 | Berkeley Lights Emeryville, CA Electrical Engineer BSEE/MSEE degree or equivalent Exp: 0-3 years |
Berkeley Lights is looking for a dynamic and energetic person to fill the role of Electrical Development Engineer. As a member of our Hardware Engineering team, you will be responsible for contributing to the hardware development of our commercial product offerings. This person must be able to work with a talented team to engineer robust solutions to our toughest problems. This person must be passionate about engineering, a quick learner, and love working at a dynamic startup company that will change the world! | 11/15/2022 |
| 5736 | BGI San Jose, CA LC/MS Research Associate – Small Molecule B.S. degree with biochemistry/chemistry major or related field Exp: 0-2 years |
San Jose Mass Spec Lab of BGI Americas is seeking an exceptional and motivated research associate with competitive compensation. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up metabolomics and lipidomics capability in SJMS lab, 4) to support other departments when needed. A candidate with metabolomics/lipidomics LC-MS experience is a plus; a candidate with small molecule sample prep experience is a plus. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for metabolomic or lipidomics analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and working with biofluids is a plus. | 11/15/2022 |
| 5737 | BGI San Jose, CA LC/MS Research Associate – Proteomics B.S. degree with biochemistry/chemistry major or related field Exp: 0-2 years |
BGI Americas San Jose Mass Spec (SJMS) center is seeking an exceptional and motivated research associate to join our Proteomics department at our San Jose facility. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up additional proteomics capability in SJMS lab, 4) to support other departments when needed. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for proteomics and biologics characterization analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and, working with biofluids is a plus. | 11/15/2022 |
| 5738 | BigHat Biosciences San Mateo, CA Research Associate (Production) BS in Biology or Chemistry Exp: 1+ year(s) |
BigHat Biosciences is seeking a self-motivated individual for a Research Associate, Production role to execute key experiments and optimize protocols to fuel BigHat’s high-throughput, automated platform for producing and characterizing antibodies. | 11/15/2022 |
| 5739 | BioAssay Systems Hayward, CA Research Associate - Assay Development A bachelors degree in biochemistry, chemistry, biology, or related field Exp: 1-2 years |
We currently have an exciting opportunity for an enthusiastic research associate to join our growing R&D team. This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers. This is a fantastic opportunity for a motivated recent graduate to be part of a successful and expanding team while learning a number of laboratory skills in a supportive environment. In addition, working on service projects will expose the candidate to multiple other companies and research areas. Moreover, as a small company we offer ample opportunities for professional growth and faster than average promotions. | 11/15/2022 |
| 5740 | BioAssay Systems Hayward, CA Research Associate - Manufacturing college degree in chemistry, biochemistry or biology Exp: 1-2 years |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing, and packaging the finished products. This candidate may also join part time in our R&D team. | 11/15/2022 |
| 5741 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II B.S. in molecular biology, biology, biomedical sciences, or a related field is desired Exp: 0-2 years |
The Molecular Systems Research Associate I or II (RA I/II) position is a full-time, non-exempt position. This position is part of a team working on various laboratory procedures involving nucleic acid isolation methods and PCR under general guidance. This person will work closely with other research associates or scientists in the research lab. | 11/16/2022 |
| 5742 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II Bachelor’s degree with emphasis in science. Exp: RAI: 0-2 years |
The Research Associate I/II is a technical hourly position with laboratory responsibilities. The RA II works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of FDA and other regulatory submissions. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). | 11/16/2022 |
| 5743 | BioFire Diagnostics Salt Lake City, UT Research Associate I bachelor’s degree with an emphasis in science is preferred. Exp: entry-level |
The Research Associate I is a technical, hourly position with laboratory responsibilities. The RA I works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). | 11/16/2022 |
| 5744 | BioFire Diagnostics Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline Exp: 0-2 years |
This is a full-time non-exempt position. This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. This person works closely with other research associates in the department. Performs general lab duties, designs and conducts experiments, collects and analyzes data, and keeps an accurate record of all work done in accordance with the quality system. Requires some problem-solving skills. Normally receives general instructions on routine work and detailed instructions on new assignments. Reports to the Senior Research Associate or Scientist. | 11/16/2022 |
| 5745 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II B.S. in biology, biomedical sciences, chemistry, or a related field Exp: 0-2 years |
The Molecular Systems Research Associate I or II (RA I/II) position is a full-time, non-exempt position. This position is part of a team working on various laboratory procedures involving nucleic acid isolation methods and PCR under general guidance. This person will work closely with other research associates or scientists in the research lab. | 11/16/2022 |
| 5746 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II Bachelor’s degree in a scientific discipline Exp: 0-2 years’ |
This is a full time non-exempt position. This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. This person works closely with research associates in the research lab. Performs general lab duties, designs and conducts experiments, collects and analyzes data and keeps an accurate record of all work done in accordance with the quality system. Requires some problem solving skills. Normally receives general instructions on routine work, detailed instruction on new assignments. Reports to a senior research associate (RA IV or above) or a Scientist. | 11/16/2022 |
| 5747 | BioLegend San Diego, CA Research Associate I - Immunoassay BS in a Biology, Chemistry or other related field Exp: 1 year |
This position is responsible for supporting immunoassay products development and manufacturing in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working with an experienced scientist on testing new hybridoma clones, qualifying the raw materials used for immunoassay products manufacturing and new immunoassay product development and launching. These immunoassay products may allow simultaneously detection of up to 13 important biomarkers for inflammatory diseases, stem cells, cancer, cardiovascular disease or neuron degenerative diseases, and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experiences in growing business in a fast-pace biotech industrial environment. He or she will be able to manage the assigned function and tasks with great communication skills in a timely manner with independence after appropriate training. | 11/16/2022 |
| 5748 | bioMerieux Durham, NC Analytical Chemist (LC-MS/MS) Degree in Chemistry or applicable Life Sciences with B.S Exp: 1-3 years |
Participate and assist in planning and conducting activities to develop new products or methods/techniques within BioMerieux Clinical Microbiology product portfolio in full compliance with current quality and safety standards Provide technical assistance for activities to improve or support existing products, methods or techniques | 11/16/2022 |
| 5749 | BioReliance St Louis, MO cGMP Associate Production Scientist Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or other life science discipline Exp: 1+ year |
The Associate Production Scientist at MilliporeSigma is responsible for the manufacturing of active biopharmaceutical ingredients (APIs) Chemicals and bulk pharmaceuticals regulated by the Food and Drug Administration (FDA). The Associate Scientist is responsible for following manufacturing protocols, consistent with and established according to current Good Manufacturing Practices (cGMP) and ensuring the accuracy of documentation. | 11/16/2022 |
| 5750 | BioReliance St Louis, MO cGMP Associate Production Scientist Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or other life science discipline Exp: 1+ year |
The Associate Production Scientist at MilliporeSigma is responsible for the manufacturing of active biopharmaceutical ingredients (APIs) Chemicals and bulk pharmaceuticals regulated by the Food and Drug Administration (FDA). The Associate Scientist is responsible for following manufacturing protocols, consistent with and established according to current Good Manufacturing Practices (cGMP) and ensuring the accuracy of documentation. | 11/17/2022 |
| 5751 | BioReliance Branchburg, NJ Process Excellence Engineer Bachelor’s Degree or Master’s Degree in Chemistry, Chemical Engineering, Materials Science, or other scientific or technical discipline Exp: 1+ years |
We are seeking an engineer who is capable of effectively leveraging their knowledge and experience in product development and quality systems to deliver products (photoresists, coatings, ancillaries) to customers in the semiconductor industry. | 11/17/2022 |
| 5752 | BioReliance Rocklin, CA Histology Lab Manufacturing Technician Bachelors’ Degree in Chemistry, Biology, or other Biological Science discipline Exp: 1+ years’ |
At MilliporeSigma, the Histology Lab Manufacturing Technician is responsible for performing Histology related functions. This includes microtomy, staining of tissue by immunohistochemistry (IHC), tissue processing and embedding. The ideal candidate has experience using a microtome and is eager to work as a team to meet departmental goals and deadlines. This position reports to the Manufacturing Supervisor as part of the Operations team located at the Rocklin Site, where we manufacture products for use in in vitro diagnostic (IVD) IHC. | 11/17/2022 |
| 5753 | BioReliance Miamisburg, OH Associate Production Scientist Bachelor’s Degree in Chemistry, Biochemistry, or other Science discipline Exp: <1 year |
As an Associate Production Scientist in Miamisburg, OH, you will manufacture or evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department. | 11/17/2022 |
| 5754 | BioReliance Sheboygan Falls, WI Associate Quality Control Chemist (Laboratory) Bachelor’s Degree in Chemistry, Biochemistry,?Chemical Engineering, or other Life Science discipline Exp: <1 year |
The Associate Quality Control Chemist (Lab) will evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 11/17/2022 |
| 5755 | LGC Biosearch Technologies Cumberland, ME Manufacturing Chemist I (47324) Bachelors degree in life science field or other related science or medical curriculum Exp: no formal experience |
The Manufacturing Chemist I fulfils the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 11/17/2022 |
| 5756 | LGC Biosearch Technologies Petaluma, CA Therapeutic Production Technician I - Entry Level- Day Shift (47172) Bachelors degree preferred with a Science background Exp: 1 or more years’ |
The Therapeutic Production Technician will support oligonucleotide manufacturing processes in the LGC Biosearch Technologies’ Petaluma Therapeutic GMP suite. Activities include: daily calibration of instruments, stocking materials, cleaning and maintaining labware. | 11/17/2022 |
| 5757 | LGC Biosearch Technologies Petaluma, CA Quality Control Analyst - Chem Lab (47184) Bachelor’s degree in relevant field such as chemistry, biochemistry, chemical engineering, pharmaceutical sciences Exp: 1 years |
The Quality Control Analyst focus on the performance of analytical testing activities within the QC Chemistry lab. They are responsible for testing intermediate and finished chemical products, analysing the results of Quality Control testing, and comparing results to established specification and customer requirements. In addition, they perform testing and/or review of incoming goods. This position reports to the Quality Control Supervisor/Quality Control Manager. | 11/17/2022 |
| 5758 | LGC Biosearch Technologies Manchester, NH Assistant Chemist 1 (47120) Bachelor of Science degree, chemistry is preferred Exp: 0-2 years |
Prepare aqueous and/or metallo-organic stock and custom samples per QSPs Follows standard operating procedures Operates basic laboratory equipment including lab balances and analytical instrumentation as trained Follows, as well as possesses, strong written and verbal instructions Follows complex procedures and operations Demonstrates consistent, reliable performance Works effectively as part of a team as well as independently with minimal supervision Exhibits organizational skills and attention to detail Demonstrates math and computer skills Meets production goals Learn quickly and is easily trainable Maintains the ability to problem solve and apply retained knowledge Exemplify the LGC core values on a day-to-day basis Perform other duties as assigned Ability to learn chemical nomenclature, properties and proper handling of chemicals | 11/17/2022 |
| 5759 | Bio-techne Minneapolis, MN Advanced Research Associate Master’s degree in a related field Exp: up to 2 years |
This position is responsible for participating in the development of Bio-Techne's various product lines. You will maintain knowledge of multiple products and procedures as well as draft and revise standard operating procedures in order to further the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 11/17/2022 |
| 5760 | Aldevron Danvers, MA Research Associate IHC BSc or BA in a Scientific discipline Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure | 11/7/2022 |
| 5761 | Aldevron Coralville/ Des Moines, IA Research Scientist II - Verification and Validation Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field) Exp: one or more years |
Purpose Statement: The Research Scientist II, under minimal supervision, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with the development and characterization of new IDT genomics products in NGS, qPCR and functional genomics. This position is responsible for planning and executing experiments, analyzing data and reporting/presenting findings as well as supporting IDT customers. This individual will aid in the development and characterization of new genomics products in NGS and qPCR to help create cutting edge, robust new products, and assays for basic research, agricultural, and clinical applications. The preferred candidate will have previous bench level experience in a research or industry setting and strong knowledge in basic laboratory and molecular biology techniques. Background in next-generation sequencing and/or qPCR are a plus. | 11/7/2022 |
| 5762 | Aldevron Sunnyvale, CA Scientist II Master’s degree in Molecular biology/Bioinformatics or related field Exp: 1+ years |
The Scientist II is responsible for planning, executing, and discussing experiments that drive product development. As a Scientist II, the employee has opportunities to learn Cepheid integrated platforms and technology with the goal of developing infectious disease tests to meet existing and emerging customer needs. This position is part of Cepheid’s Infectious Disease R&D and will be located in Sunnyvale, CA. The Infectious Disease R&D Business Unit is comprised of research and development scientists driving New Production Introduction (NPI) that aligns with Cepheid’s strategic plan to fortify our leadership position in the Molecular Diagnostic market. | 11/7/2022 |
| 5763 | AllCells Huntsville, AL Laboratory Technician I - CP Bachelor of Science degree in biology (or related field) or 2 yr MLT degree with ASCP certification Exp: 1-3 years |
Position Summary: The Laboratory Technician I- Cell Processing, contributes to our mission by processing biospecimen samples for cryopreservation or further characterization based on standard operating procedures. Hours are approximately 9am-6pm, but can fluctuate based on business needs. Includes a Saturday rotation. | 11/7/2022 |
| 5764 | AllCells Huntsville, AL QC Specialist I - Cell & Gene Therapy Bachelors of Science in Biology, Microbiology, or other life sciences related field Exp: 0-2 years’ |
The Quality Control Specialist I is responsible for testing, inspection and release of materials and finished products, will execute routine in-process and final product analysis, in accordance with specific procedures and specifications. | 11/7/2022 |
| 5765 | AllCells Huntsville, AL Laboratory Technician I - CGT Bachelor of Science degree in biology or related field or 2 year MLT degree with ASCP certification Exp: 1-3 years |
Position Summary: The Laboratory Technician I- Cell and Gene Therapy, contributes to our mission by processing blood samples collected through leukapheresis for cryopreservation or further characterization based on standard operating procedures. Hours are approximately 10am-7pm, but can fluctuate based on business needs. | 11/7/2022 |
| 5766 | AllCells Newtown, PA Histology Technologist Master's degree in a laboratory science (i.e. biology, chemistry, or other lab science) Exp: |
The Histology Technologist contributes to our mission by supporting the Study Director throughout the duration of a project including sponsor and study director updates, developing study design, assisting with proposal writing, and presenting to clients. | 11/7/2022 |
| 5767 | Allogene Therapeutics South San Francisco, CA Associate Scientist, In Vivo Pharmacology Master of Science degree Exp: 1+ years |
We are seeking a hard-working, enthusiastic Associate Scientist/Senior Associate Scientist to contribute to developing next-generation AlloCAR T cells for the treatment of hematologic malignancies and solid tumors. You will be working closely with researchers to support preclinical in vivo studies utilizing tumor xenograft models. The successful candidate will have extensive experience working with mice and will have the opportunity to learn new in vitro skills, developing experience in flow cytometry for CAR T cell pharmacokinetics. The ideal candidate will show the ability to conduct in vivo studies with minimum supervision and to generate high-quality data to support Allogene’s pipeline. | 11/7/2022 |
| 5768 | Allogene Therapeutics South San Francisco, CA Associate Scientist/Scientist, Protein Science/Antibody Engineer BS. or MS. degree in life science or related field required (or relevant experience) Exp: 1+ years |
Allogene Therapeutics is seeking a highly motivated Associate Scientist/ Scientist in the Protein Science group to support the antibody/protein engineering, production, conjugation, and characterization needs across all our research and development programs. The position will report to the Sr Principal Scientist, Protein Engineering and be responsible for continuing our development and implementation of these core capabilities in support of our pipeline of allogeneic CAR T cells. The ideal candidate is an individual who is interested in working in a fast-paced, dynamic, and highly collaborative biotech environment with a willingness and ability to successfully take on new challenges. | 11/7/2022 |
| 5769 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, Translational Research B.S/M.S. degree in a biological discipline such as Molecular Biology, Cell Biology or Biochemistry Exp: 0-3 years |
We are seeking a talented and enthusiastic candidate to fill an Associate Scientist II position within Alnylam’s Discovery and Translational Research team based in Kendall Square, Cambridge MA. This position is an opportunity to potentially see one’s work progress from the bench to the clinic and positively impact patients’ lives. This position involves performing exploratory work and preclinical target validation as part of a multidisciplinary team involved in the discovery of RNAi compounds for a variety of novel indications and support their entry into the clinic. The successful candidate will have a passion for science, attention to detail and desire to learn about new disease areas and lab techniques. Experience or willingness to learn in vivo rodent techniques is required. | 11/7/2022 |
| 5770 | Alpine Immune Services Seattle, WA Research Associate/Senior Research Associate, Biomarkers Bachelors or Masters Exp: 1+ years |
Alpine Immune Sciences is seeking an enthusiastic and highly motivated Research Associate|Senior Research Associate to join the Clinical Biomarker group. This individual will be primarily responsible for supporting flow cytometry and other biomarker analysis of clinical samples to support our protein-based immunotherapeutics platform. The successful candidate must have hands-on experience with design and analysis of multicolor flow cytometry panels. Excellent written and oral communication skills, effective team contribution, and strong organizational skills are essential. | 11/7/2022 |
| 5771 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 11/7/2022 |
| 5772 | Amarex Clinical Research Ypsilanti, MI Technician II - Engineering Lab Technician Bachelor or Associate degree in an Engineering or Scientific discipline Exp: One year |
As a Technician II for the Engineering/Plastics Lab, you will be responsible for conducting basic testing on plastics, pipes, fittings and other related plumbing products to specific standards and procedures. | 11/7/2022 |
| 5773 | AmbioPharm North Augusta, SC QC Chemist III Masters Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Hands on experience with HPLC/UPLC, GC, GC-MS, IC, KF and other routine analytical equipment such as pH meter and balance. Perform quality control routine critical testing for raw material/ Intermediate/ Release / Stability testing and evaluate stability trends. Ensure completion of all the testing release , stability and validation work in timely manner. Perform Method development and method validation execution, including writing protocols and reports. Must be proficient. Responsible for reviewing analytical laboratory raw data and electronic records. Assist the QC group with writing and editing of deviations, CAPA, OOS and OOT. Maintain the QC lab by ordering supplies routinely used for testing. Assist the QC/QA group with writing and editing of SOPs and STPs. Assist in equipment qualification and troubleshooting Train and assist junior chemist to ensure completion of testing Other duties as assigned | 11/7/2022 |
| 5774 | AmbioPharm North Augusta, SC QC Chemist I Bachelor’s Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Perform and review QC release testing. Support routine analytical testing using GC, KF, and HPLC. Assist the QC/QA group with writing and editing of SOPs and STPs Support analytical method development. Perform method transfer and validation activities. Perform OQ/PQ for the Quality Control Equipment. Other duties as assigned | 11/7/2022 |
| 5775 | AmbioPharm North Augusta, SC QC Chemist II Master’s Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Perform and review QC release testing. Support routine analytical testing using GC, KF, and HPLC. Assist the QC/QA group with writing and editing of SOPs and STPs Support analytical method development. Perform method transfer and validation activities. Perform OQ/PQ for the Quality Control Equipment. Other duties as assigned. | 11/8/2022 |
| 5776 | AmbioPharm North Augusta, SC QA Analytical Associate II Bachelors Science Degree is required. (Chemistry, Biology, or other Life Science degree) Exp: 0+ years |
Quality Assurance review and approval of analytical data for release of CGMP manufacturing batches (UPLC, HPLC, IC, etc) Review of instrument audit trails for compliance Quality Assurance review and approval of analytical method protocols, validations and reports (UPLC, HPLC, IC, etc) Creation of CoAs for analytical testing Review and approval of analytical change controls and deviations and CAPAs Perform internal facility and quality system audits. Assist with SOP revisions and writing new SOPs. Other duties as requested by the Quality Management. | 11/8/2022 |
| 5777 | AmbioPharm North Augusta, SC Microbiologist BS in Microbiology or life sciences. Exp: 1-5 years |
Perform procurement and testing of: city and pharmaceutical grade water per USP guidelines and SOP; product for bioburden, endotoxin per USP guidelines and SOP; stability samples per SOP; environmental monitoring sample (viable and non-viable) per USP guidelines and SOP, as scheduled (daily, weekly, monthly, quarterly) Support production in qualification of clean rooms and water systems. Data entry for trending reports Perform QC testing and release of microbiological media, reagents, and stock cultures Maintenance of stock cultures Use of aseptic technique for sampling and testing of all samples collected for microbiological analysis Documentation of all activities per current good documentation practices as described in SOP Use basic understanding of and knowledge of techniques, instrumentation and lab functions to identify problems, initiate investigations and support completion of work assignments | 11/8/2022 |
| 5778 | AmbioPharm North Augusta, SC Research & Development Chemist I BS/BA in chemistry or related field Exp: 1 year |
Assist in performing peptide synthesis using commercial peptide synthesizers. Monitor upstream process progress via HPLC, UPLC, LC/MS, and other qualitative methods. Support routine analytical testing and analytical method development activities using HPLC/UPLC. Assist in preparative scale chromatography for peptide purification development or non-GMP activities. Responsible for recording and reporting Research and Development results in a suitable proposal format as deemed appropriate in support of new and existing products. Assist with the coordination and execution of equipment qualification activities in accordance with regulatory requirements. As needed, work in a GMP environment to assist in the transfer of peptide manufacturing process and analytical development strategies. As needed, follow approved instructions such as Batch Records, Standard Operation Procedures, Standard Test Procedures, etc. operate and maintain equipment for Research and Development, manufacturing and in-process testing as needed. | 11/8/2022 |
| 5779 | Ambys Medicines South San Francisco, CA Research Associate / Senior Research Associate, Pharmacology Bachelor’s degree Exp: 1+ years |
We are seeking a collaborative and detail-oriented Research Associate to join our Pharmacology group. You will contribute as part of a multidisciplinary team to develop novel therapies to treat liver diseases using cell therapy strategies. In this position, you will report to our In Vivo Manager and will work in a team environment performing a variety of tasks and experiments in support of our in vivo pharmacology studies. | 11/8/2022 |
| 5780 | Ambys Medicines South San Francisco, CA Associate/Senior Associate, Quality Control, Cell Therapy BS or MS degree in a biological science discipline Exp: 1-5 years |
Our Technical Operations team is growing, and we have an exciting opportunity for a talented and motivated Quality Control Associate I/II to support our cell and gene therapy manufacturing activities. You will contribute as part of a multidisciplinary team to develop novel cell therapies to treat liver diseases using cell and gene therapy strategies. In this position, you will be critical to the overall strategy and growth of the CMC organization at Ambys as we build out a new cGMP facility. You will report to our Manager, Quality Control Method Transfer, and Validation. You will be responsible for helping develop and execute cGMP-compliant testing of manufactured hepatocytes for supporting process development, IND-enabling studies, and clinical studies. | 11/8/2022 |
| 5781 | Ambys Medicines South San Francisco, CA Microbiology Analyst, Quality Control Bachelor’s degree in microbiology, biology, or chemistry. Exp: 0-3 years |
Our Technical Operations team is growing, and we have an exciting opportunity for a talented and motivated Microbiology Analyst for Quality Control to support our cell therapy manufacturing activities. You will contribute as part of a multidisciplinary team to develop novel cell therapies to treat liver diseases using cell therapy strategies. In this role, you will provide support to Quality Control Department projects as needed activities for the new cGMP facility. | 11/8/2022 |
| 5782 | AnaSpec Fremont, CA Research Associate-Assay Kits BS in Biochemistry, Chemistry, Cell Biology or related discipline Exp: 0-3 years |
Perform assay kit production and QC tests: enzyme activity assays, protein labelling and conjugation, protein expression/purification Manage routine activities, including meticulous record keeping Order laboratory supplies and reagents, maintain inventory Participation in R&D projects expected Ensure implementation, compliance, and continuous improvement of QMS through SOP documentation. | 11/8/2022 |
| 5783 | AnaSpec Fremont, CA Research Associate-Antibodies BS in Biochemistry, Chemistry, Cell Biology or related discipline Exp: 0-3 years |
Perform antibody purification and characterization, protein expression/purification; protein/peptide labeling and conjugation Manage routine activities, including meticulous record keeping Order laboratory supplies and reagents, maintain inventory Participation in R&D projects expected Ensure implementation, compliance, and continuous improvement of QMS through SOP documentation Other duties as assigned by Management | 11/8/2022 |
| 5784 | AnaSpec Fremont, CA Synthesis Chemist I BS or above in Chemistry, Organic Chemistry, or related disciplines Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). As a member of the Synthesis department, the Synthesis Chemist I will work closely with the Purification, QC, and Sales & Business Development departments. | 11/8/2022 |
| 5785 | ANI Pharmaceuticals Baudette, MN QC Chemist/Sr. QC Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: QC Chemist – 1-3 years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 11/8/2022 |
| 5786 | Ansh Labs Webster, TX Scientist (R&D) Master’s degree in Biological/Chemical Sciences/Biotechnology or related area Exp: 1 year |
As a key member of the R&D Department, this individual will provide critical scientific skills to assist in the development and scale-up of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays, Lateral Flow assays and micro fludics based immunoassays). | 11/8/2022 |
| 5787 | Aquinnah Pharmaceuticals Cambridge, MA RESEARCH ASSOCIATE Master’s degree in neuroscience, cell biology or related discipline Exp: 1+ years |
This position is laboratory-based and requires strong experimental skills with a background in cell biology, molecular biology, or biochemistry. Under supervision, the candidate will assist in duties including, but not limited to: cell culture maintenance, compound screening, biochemical assays, immunocytochemistry, and analysis using state of the art high-content imaging. Strong communication skills are required including the ability to analyze and report on the results. The candidate will be expected to function efficiently and cooperatively within a team and maintain accurate and clear project records. The ideal candidate will be creative, energetic and motivated. Candidates should have a Bachelor’s or Master’s degree in neuroscience, biology, or related field. Salary will be competitive and commensurate with experience. | 11/9/2022 |
| 5788 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 11/9/2022 |
| 5789 | ArunA Biomedical Athens, GA Process Development Associate II MS degree in relevant field Exp: 0-2 years' |
• Set up and execute experiments related to process development • Set up and execute experiments associated with scale-up production processes • Troubleshoot experiment errors and assist in root-cause analyses to determine the source of error • Perform data analysis, identify trends, and incorporate findings into development and control strategies. • Manage multiple projects simultaneously with minimal supervision • Troubleshoot software or equipment malfunction to determine the source of error. • Ability to use a variety of equipment such as pipettors, balances, laminar flow hoods, incubators, autoclaves, microscopes, centrifuges, plate readers, and particle analyzer. • Maintain detailed records that are legible, accurate and readily understood. • Complete documentation needed to support development procedures including data capture forms, equipment logbooks, or inventory forms. • Compile laboratory test data and perform appropriate analyses. | 11/9/2022 |
| 5790 | ArunA Biomedical Athens, GA Analytical Development and Quality Control Associate II MS degree in relevant field Exp: 0-2 years' |
• Conduct routine analyses of in-process materials, drug substance, drug product and stability samples following written procedures. • Expand skill set of analytical technologies and test methods and assist in the development of test methods. • Participate as an analyst in qualification/validation of various biological and chemical QC assays. • Ability to perform aseptic technique and mammalian cell culture. • Perform data analysis, identify trends, and incorporate findings into development and control strategies. • Manage multiple projects simultaneously with minimal supervision • Troubleshoot software or equipment malfunction to determine the source of error. • Ability to use a variety of equipment such as pipettors, balances, laminar flow hoods, incubators, autoclaves, microscopes, centrifuges, plate readers, and particle analyzer. • Maintain detailed records that are legible, accurate and readily understood. • Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms. • Compile laboratory test data and perform appropriate analyses. • Report questionable test results and participate in OOS and failure investigations. • Excellent communication skills and professional/technically proficient • Must take the initiative as problems and/or opportunities arise | 11/9/2022 |
| 5791 | Arvinas New Haven, CT Associate Scientist, Platform Biology B.S./M.S. in Biology or related field Exp: 1-4 years |
We are looking for a motivated individual to join our Platform Biology team as an Associate Scientist. This position will be dedicated to conducting experiments and executing assays involving cultured cells or isolated proteins and using multiple methodologies to develop protein degrader small molecules. This is a committed bench scientist position located at our headquarters in New Haven, CT and reports to the Senior Research Investigator in our Platform Biology group. | 11/9/2022 |
| 5792 | Arvinas New Haven, CT Research Associate, Platform Biology B.S./M.S. in Biology or related field Exp: 0.5-2 years |
We are looking for a motivated individual to join our Platform Biology team as a Research Associate. This position will be dedicated to conducting experiments and executing assays involving cultured cells or isolated proteins and using multiple methodologies to develop PROTAC protein degrader small molecules. This is a committed bench scientist position located at our headquarters in New Haven, CT, and reports to a Senior Research Scientist in our Platform Biology group. NOTE: This position is a temporary role to cover an individual while out on maternity leave. This is a terrific opportunity to demonstrate technical capabilities and establish a network within Arvinas for potential future opportunities! | 11/9/2022 |
| 5793 | Atalanta Therapeutics Boston, MA Associate Scientist I/II, In Vitro Biology, Platform Development Bachelor’s degree in a relevant biological science; OR a Master’s degree in biochemistry or relevant biological science Exp: BS: 1 year; MS: 0-2 plus |
Atalanta is seeking a highly motivated individual to join our In Vitro Biology team to contribute to the preclinical development of RNAi-based therapeutics. The selected individual is expected to design and execute biochemical assays for the quantification of therapeutic oligonucleotides, transcriptional profiling while supporting the development of our internal RNAi platform. This role requires a highly collaborative and entrepreneurial mindset that will interact with multiple areas across Atalanta’s research. | 11/9/2022 |
| 5794 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, In Vitro Biology Master’s degree in biochemistry or relevant biological science Exp: 0-2 plus |
Atalanta is seeking a highly motivated Associate Scientist II/Senior Associate Scientist to join our In Vitro Biology team to contribute to the preclinical development of RNAi-based therapeutics. This individual is expected to design and execute assays for the identification of therapeutic oligonucleotides, to assess the knockdown of target mRNAs and proteins and to assess additional molecular biomarkers of therapeutic efficacy. | 11/9/2022 |
| 5795 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, In Vivo Pharmacology Master’s degree Exp: 0-2 plus years |
Atalanta is seeking a highly skilled and motivated Associate/Senior Associate Scientist to join the in vivo pharmacology group to support Atalanta’s drug discovery programs. This individual will extensive hands-on experience in performing survival surgeries (stereotaxic or direct intraparenchymal injection preferred), pharmacological administration, brain and tissue collection, and in processing CNS tissue and molecular analysis to assess target gene and protein expression. We are seeking candidates who thrive in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. The Associate/Senior Associate Scientist will be responsible for assay development and execution of experiments to determine the biodistribution, pharmacodynamic properties and efficacy of oligonucleotides in research and preclinical studies supporting multiple drug discovery programs and platform discovery research. | 11/9/2022 |
| 5796 | Atalanta Therapeutics Boston, MA Associate Scientist/Senior Associate Scientist, Oligonucleotide Chemistry Bachelor’s degree in Chemistry or related scientific discipline Bachelor’s degree in Chemistry or related scientific discipline; -OR- a Master’s degre Exp: BS: 1 year; MS: 0-2 years |
The candidate will join a dynamic team responsible for the design and synthesis of oligonucleotides for Atalanta’s drug discovery programs. Successful candidates will have experience with modern laboratory equipment, and spectroscopic analysis, preferably in relation to oligonucleotides, as well as demonstrated ability to work as part of an integrated team on multiple parallel projects. This individual will be responsible for the independent operation and maintenance of instruments to synthesize, purify, and analyze chemically modified oligonucleotides as well as prepare samples for in vitro and in vivo studies. The ideal candidate is personable, organized, and thrives in a fast-paced environment. This role provides the right candidate with the opportunity to take on increasing responsibility over time within Atalanta’s Chemistry function. | 11/9/2022 |
| 5797 | Atara Biotherapeutics Thousand Oaks, CA Sr. Research Associate / Associate Scientist - Analytical Development Research Associate: BS in Immunology, or biological sciences Exp: 1 year |
The Research Associate or Sr. Research Associate under supervision will be required directly to participating and performing in laboratory activities to support the design, development, and qualification/Validation of bioanalytical methods and cell-based assays for characterization, in-process and lot release testing of engineered T cell drug products and their impurities. This role will be involved in assay optimization and standardization and assay transfer to QC team. Will be expected to perform assay development experiments, document methods and materials, write technical reports and communicate findings. This role is expected in cross-functional collaboration with other departments as needed. | 11/9/2022 |
| 5798 | Atreca San Carlos, CA RESEARCH ASSOCIATE II/SR. RESEARCH ASSOCIATE, IN VIVO PHARMACOLOGY MS Exp: 1+ years |
Atreca is a dynamic biotechnology company whose Immune Repertoire Capture™ technology enables the discovery and development of novel cancer immunotherapeutics. Atreca is looking for a talented and self-motivated SRA/Associate Scientist to join its In Vivo Pharmacology team. The RAII/SRA will apply his/her expertise to Atreca's oncology preclinical research program. The successful candidate will have the opportunity to interact and collaborate with a multidisciplinary team in a dynamic and fast paced scientific environment. In this role, the RAII/SRA will perform multiple efficacy studies testing various therapeutic agents and combination regimens in mouse tumor models. Job title/compensation commensurate with experience and qualifications. | 11/10/2022 |
| 5799 | Avance Biosciences Houston, TX Laboratory Associate II Bachelor’s degree in biological sciences Exp: 1 year |
Carry out Molecular Biology, Microbiology, Protein experiments following established SOPs and/or guidance of laboratory management. Perform DNA/RNA extraction, quantification, and gel QC. Perform PCR setup for qualitative and quantitative analysis Report experimental results to project managers in a timely manner. Follow established quality management policies and GLP and GMP practices. | 11/10/2022 |
| 5800 | Sorrento Therapeutics San Diego, CA QC Microbiology Associate Bachelor’s degree in Microbiology (or equivalent education/experience) Exp: 1-2 years |
Provide microbiological support and testing of cGMP environments as well as contributing to WFI testing, bioburden and sterility testing. | 10/30/2022 |
| 5801 | Sorrento Therapeutics San Diego, CA Research Associate Bachelor's Degree in Life Sciences or a related field. Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking a Research Associate who, under close supervision assists in conducting laboratory experiments, maintain laboratory environment, organizing data, and analyzing results. Major tasks include: antibody discovery by phage display, antibody expression and purification, antibody characterization, cell culture and cell based assay | 10/30/2022 |
| 5802 | Sorrento Therapeutics San Diego, CA Research Associate - Process Development & Manufacturing Bachelor’s Degree in Molecular Biology or related disciplines Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking a Process Development and MFG Research Associate position to help with protein production and DNA plasmid cGMP production in microbial system including process development and manufacturing. Major tasks include: Buffer preparation, bacteria culture including fermentation in bioreactor and harvest, bacteria lysis and protein and plasmid DNA purification. | 10/30/2022 |
| 5803 | Swift Biosciences Danvers, MA Research Associate IHC BSc or BA in a Scientific discipline Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure | 10/31/2022 |
| 5804 | Swift Biosciences Carlsbad, CA Development Scientist I Bachelor of Science degree in Biology, Microbiology, Chemistry, Biochemistry or related science Exp: 0+ years |
The Development Scientist I for Beckman Coulter Diagnostics is responsible for helping to Develops methods for the production and testing of new products. Develops new product designs, processes, new product scale-up, design/product optimization, technology transfer and process/product validation activities. Develops production procedures and process/product specifications. This individual will perform experimental studies, collect and evaluate the data, and communicate the results towards this goal. In addition, this individual will support both continuous improvement activities and current market products. This position is part of Research & Development located in Carlsbad, CA and will be On-Site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. | 10/31/2022 |
| 5805 | Tara Biosystems Lexington, MA Associate Scientist, High-throughput Medicinal Chemistry BS or MS in Chemistry, or related subject Exp: 0 – 2 years |
We are looking for a highly motivated chemist to join our High Throughput Medicinal Chemistry teams. This individual will be responsible for the synthesis of small molecules (singletons & libraries) in support of our Medicinal Chemistry programs. | 10/31/2022 |
| 5806 | Tectonic Therapeutic Watertown, MA Research Associate/Senior Research Associate – Protein Sciences (Protein Biophysics) Bachelor’s or Master’s degree in analytical or biophysical chemistry or related discipline Exp: 1-3 years 1-3 years 1-3 years |
The (Senior) Research Associate for Tectonic will be a highly collaborative team player who has experience characterizing proteins using a wide array of analytical and biophysical techniques. Hands-on experience with standard biophysical techniques is required and experience with assay development is a plus. The successful candidate will contribute to our core research capabilities and the development of our anti-GPCR antibody discovery platform. The candidate would conduct established biophysical assays and perform continuous development and improvement over time. This position represents a unique opportunity for the successful applicant to join an innovative start-up at the heart of the Boston biotech ecosystem and to contribute to its long-term Success. | 10/31/2022 |
| 5807 | Thrive Earlier Detection Madison, WI Research Associate I, Advanced Research and Technology Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate I, with guidance from more experienced scientists, assists in the day to day experimental work that includes execution of bench experiments, and gathering and assembling of data. Working in a team setting, the Research Associate I will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 11/1/2022 |
| 5808 | Thrive Earlier Detection Cambridge, MA Research Associate I Research Associate I Research Associate I Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate I, with guidance from more experienced scientists, assists in the day to day experimental work that includes execution of bench experiments, and gathering and assembling of data. Working in a team setting, the Research Associate I will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 11/1/2022 |
| 5809 | Trevigen San Marcos, CA Research Associate - Advanced Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field preferred Exp: 1-5 years |
Responsible for developing controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for developing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to research in a laboratory environment. | 11/1/2022 |
| 5810 | Trevigen Minneapolis, MN Research Associate, Microbiology QC Bachelor’s degree in Microbiology or a related scientific field or equivalent Exp: up to 3 years |
The responsibilities of this position are to participate in the Microbiology QC testing and reporting procedures: set up, read, and report the microbial QC bioburden and sterility testing of various sample types using culture methods that include direct plating, broth inoculation, and membrane filtration. Performance of environmental monitoring for viable microbes, particle counts, and WFI/deionized water testing, reading, and reporting. Assist with efficacy and validation testing, new procedure development, new equipment IQ/OQ and calibrations. Perform general lab duties, assist with sanitization of clean rooms, and additional duties as assigned. | 11/1/2022 |
| 5811 | Universal Cells Seattle, WA Research Associate II, Process Development MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Process Development is to execute experiments to improve clinical-grade, gene-editing processes of Universal Donor Cells and to provide data for CMC documents. This Research Associate II role will work as part of a team evaluating processes, and planning/executing experiments to evaluate all aspects of culturing, gene-editing, and processing of pluripotent stem cells. This position will be provided training to perform all required fundamental skills. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 11/1/2022 |
| 5812 | VaxCyte San Carlos, CA Associate Scientist I/II, Analytical Development for Characterization MS in Chemistry, Analytical Chemistry preferred, Organic / Biochemistry considered. Exp: 1-3 years |
Vaxcyte is looking for an energetic and talented individual to join our Analytical Development team. Primary responsibility for the incumbent will be to support the developmental activities currently on going in the laboratory as assigned. | 11/1/2022 |
| 5813 | VGXI The Woodlands, TX DOWNSTREAM PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: 0-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for downstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Downstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 11/2/2022 |
| 5814 | VGXI The Woodlands, TX UPSTREAM PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for upstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Upstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 11/2/2022 |
| 5815 | VGXI The Woodlands, TX MICROPROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for plasmid manufacturing operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Microprocess Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 11/2/2022 |
| 5816 | WaVe Life Sciences Cambridge, MA Research Associate/Scientist, Biology BS or MS degree in biology, biochemistry, cellular/molecular biology or related discipline Exp: |
Wave seeks a highly motivated biologist to join its research team in Cambridge, Massachusetts to support a rapidly expanding RNA-editing platform. This is an ideal position for an individual who is interested in working with cutting edge technologies and who thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate should have strong technical skills, and will be responsible for designing, executing, and analyzing experiments as a member of team focused on advancing therapeutic programs and discovery research platforms. | 11/2/2022 |
| 5817 | Frontage Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree Exp: 0-3 years |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 11/2/2022 |
| 5818 | Frontage Hayward, CA Research Associate-Biologics MS / MA in biochemistry, biology, chemistry, pharmaceutics or related scientific discipline Exp: 0-2 years |
Conduct study design, lab-testing, data analysis and PI review. Author and/or review methods, protocols and other related documents. Assist PIs in maintaining project quality, meeting compliance requirements and timelines. Prepare notebooks, study binders, data packets, data summaries, methods, and qualification/validation protocols under the supervision of lab management / PIs Monitor reagent and consumable inventories and timely submit the orders for the support of both project and non-project based programs After receiving sufficient training, perform as PI and manage the overall planning, execution, and quality of assigned MD/MV and sample analysis projects under the supervision of lab management Participate TC and communicate with sponsors to solve technical issues and update projects, provide weekly summary to the sponsorsConduct study design, lab-testing, data analysis and PI review. Author and/or review methods, protocols and other related documents. Assist PIs in maintaining project quality, meeting compliance requirements and timelines. Prepare notebooks, study binders, data packets, data summaries, methods, and qualification/validation protocols under the supervision of lab management / PIs Monitor reagent and consumable inventories and timely submit the orders for the support of both project and non-project based programs After receiving sufficient training, perform as PI and manage the overall planning, execution, and quality of assigned MD/MV and sample analysis projects under the supervision of lab management Participate TC and communicate with sponsors to solve technical issues and update projects, provide weekly summary to the sponsors | 11/2/2022 |
| 5819 | Frontage Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 11/2/2022 |
| 5820 | Frontage Hayward, CA Research Associate M.S. degree in related scientific discipline. Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 11/2/2022 |
| 5821 | Frontage Exton, PA Associate Scientist, Pharmaceutical Analysis, Small Molecule B.S. in Chemistry or related discipline Exp: 1-2 years |
Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines Assists method development Performs method validation under supervision Reports and resolves any unexpected issues under supervision Complies with all relevant cGMP and/or GLP regulatory requirements while carrying out assigned studiesPerforms routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines Assists method development Performs method validation under supervision Reports and resolves any unexpected issues under supervision Complies with all relevant cGMP and/or GLP regulatory requirements while carrying out assigned studies | 11/2/2022 |
| 5822 | Frontage Exton, PA Associate Scientist/scientist Associate Scientist/scientist M.S. or a B.S./B.A. Exp: 1-5 years |
This is a technical scientific position within the Biologics Service Team. The Biologics Service Team is responsible for conducting bioanalytical methods related to large molecule biotherapeutic drug development across all therapeutic areas, spanning nonclinical studies to post-market clinical development. | 11/2/2022 |
| 5823 | Frontage Exton, PA Scientist/Associate Scientist- Cell Culture B.S. or M.S. in molecular biology, biochemistry, biophysics, immunology, or a related field Exp: 1 year |
This is a bench scientific position for a competent and hardworking scientist with experience in protein purification and/or labeling of protein reagents. The person will be responsible labeling of reagents (protein and antibodies), purification and characterization including concentration estimation, SDS-PAGE, SE-HPLC, endotoxin estimations etc. He/she will be responsible for the quality of final product, record keeping and interacting with end user. The position will require excellent communication skills, and basic computer skills. | 11/2/2022 |
| 5824 | Inotiv Rockville, MD Associate Scientist I (In Vitro Cytogenetics) Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 1+ years |
Perform a wide variety of in vitro assays or tests required to characterize product or material safety Maintain sterile and good cell/tissue culture techniques Prepare study reagents in accordance with SOPs and study instructions Use and maintain scientific equipment, instrumentation and computer systems Conduct pre-designed assays using basic laboratory techniques and skills Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations Perform peer review of data and lab support records Keep the next level manager and Study Director informed of study status, technical problems and other issues which impact the lab/study Address quality audit findings and generate deviations using the quality system, as needed Receive instructions on new assignments from the laboratory manager or designee and study directors Attend pre-planning, or operational team meetings, as needed Perform other job duties, as assigned | 11/2/2022 |
| 5825 | Inotiv West Lafayette, IN Bio Analyst I B.S. in chemistry or biology Exp: one year |
Conducts sample analysis with data interpretation and basic troubleshooting. Conducts method development and method validation experiments. Assists with general housekeeping and assist other departmental personnel as necessary. | 11/02/2022 |
| 5826 | Inotiv Raleigh, NC Research Assistant A.S. or B.S. in biology or related field Exp: 0-3 years |
The Genetic Toxicology Group conducts standard and custom genetic toxicology testing and applied research supporting preclinical studies for both federal and commercial clients. | 11/02/2022 |
| 5827 | A2 Biotherapeutics Los Angeles, CA Research Associate, Drug Discovery Master’s or Bachelor’s degree in science including biology, immunology, biotechnology, or a related discipline Exp: 1-2 years |
The Drug Discovery team is seeking a highly motivated individual with experience in biochemistry, cell and molecular biology, and assay development. This is a rare opportunity to directly contribute to enabling gene therapies in broader and more challenging indications. The successful candidate will work at our research facility in Agoura Hills, CA and collaborate across multiple projects. You will join a fast-paced, dynamic and team-oriented environment and will benefit from cutting-edge scientific training, career growth, and publishing opportunities. | 11/02/2022 |
| 5828 | Abbott Scarborough, ME Reagents Scientist I Reagents Scientist I Bachelor's degree (BA or BS) in biology, immunology, or chemistry or equivalent combination of education and experience. Exp: 1-year |
The position of Reagent Scientist I is within our Abbott Rapid Diagnostics business located in Scarborough, Maine. This role will include producing antibodies for use in immunology-based chromatography and enzyme tests. The primary responsibility of the individual is the production and maintenance of the Technical Manufacturing Critical Reagent supply using Standard Operating Procedures (SOPs). | 11/3/2022 |
| 5829 | Abbott Scottsdale, AZ Electrical Engineer I Electrical Engineer I Bachelors Degree (± 16 years) Electrical/electronic engineering or related engineering field OR an equivalent combination of education and work experi Exp: six months |
Electrical Engineer I Performs entry-level activities to design and develop the layout, construction, and evaluation of a variety of prototype Printed Circuit Boards, fixtures, and tools. Identifies and routinely uses the most effective and cost-efficient business practices to execute processes. Promotes the process of continuous quality improvement and risk management and coordinates solutions for technical and project issues. Applies engineering and scientific principles to the evaluation and solution of technical problems. Exercises independent judgment in planning and organizing work; monitors performance and reports status. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. | 11/3/2022 |
| 5830 | Abbott Plymouth, MN R&D Engineer I R&D Engineer I Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, biological sciences, medical/clinical science or equivale Exp: 1+ years’ |
As R&D Engineer I, at our Plymouth, MN or St. Paul, MN location, you will be part of our Electrophysiology (EP) product development team focused on delivering the future in diagnostic, imaging, and ablation therapy catheters and EP capital equipment. This role will involve a range of responsibilities including but not limited to requirement development, testing and data analysis, and test method development and validation. | 11/3/2022 |
| 5831 | AbbVie Worcester, MA Associate Scientist I/II - Pipeline (New Grads) Bachelor’s Degree or Master’s degree. Exp: Recent Graduate |
We welcome recent graduates to apply for the Associate Scientist position, where you will generate and analyze precise, reliable, and reproducible data in a timely manner, under the direction of a more senior scientific leader. Demonstrate experimental precision and should possess general understanding of core discipline. | 11/3/2022 |
| 5832 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst I B.S. degree in a relevant scientific discipline Exp: 0-2+ years |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 11/3/2022 |
| 5833 | Adaptimmune Therapeutics Philadelphia, PA Manufacturing Cell Therapy Specialist Bachelor degree in a cell biology, bioengineering or medical technology related field, or equivalent experience is required. Exp: 1+ years’ |
This role will provide support for the manufacturing of gene modified autologous T-cell product at our manufacturing site in the Philadelphia Navy Yard. The Specialist will perform cell processing activities, media formulation, product sampling, and other manufacturing needs as necessary, commensurate with the level of training and experience of employee. Work is primarily in Grade B and Grade C aseptic manufacturing environment, but may also include support of process development runs in the Manufacturing Science and Technology laboratory. | 11/3/2022 |
| 5834 | Adare Pharmaceuticals Vandalia, OH QC Analyst Bachelor degree in Chemistry or related field Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 11/3/2022 |
| 5835 | Adare Pharmaceuticals Vandalia, OH QC Analyst (Night Shift) Bachelor degree in Chemistry or related field Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 11/3/2022 |
| 5836 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree or M.S. in Biological Sciences Exp: 1-3 years |
• Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing • Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. • Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. | 11/3/2022 |
| 5837 | Akoya Biosciences Marlborough, MA Quality Engineer, Reagents Bachelor’s Degree in Chemistry, Biology, Engineering, or a related field Exp: 1-4 years |
Akoya Biosciences is looking for a Quality Engineer to join our Quality team. The individual will manage a variety of quality system functions of Akoya Biosciences’ growing Quality Management System (QMS), working with Quality Management, product development, manufacturing, operations, and other groups, to ensure compliance to ISO 13485 and medical device quality requirements. The individual must be able to work independently and resolve or escalate quality issues in a creative, collaborative, and timely manner. Core values must include commitment to customer and operations excellence with demonstrated ethics and integrity. The Quality Engineer will manage day-to-day QMS processes such as Document Control, Change Control, Training, Supplier monitoring, CAPA, Nonconformances, and generating metrics. The individual will also help develop new processes as the QMS grows and participate in implementing a new electronic QMS system. The Quality Engineer will also participate in design quality, auditing, and will have opportunities to grow within the Quality group. This includes learning about and supporting the laboratory testing quality activities as needed. | 11/4/2022 |
| 5838 | Akron Biotechnology Sarasota, FL Manufacturing Associates (I, II, III) BA/BS or AA/AS in Biology, Chemistry, Bioengineering or a related field. Exp: 1-2 years’ |
Akron Biotech is continuing to transform and further its rapidly growing capabilities and is now seeking highly motivated professionals to join our expanding team. This is an exciting opportunity to play a critical role within our organization that is driving advanced therapy development and commercialization with high quality industrial scale solutions. We manufacture and distribute components and raw materials for cell therapy discovery, development, and commercialization to meet industry needs worldwide. We offer an array of highly competitive benefits and perks to our valued associates. Candidates will be placed as I, II and III according to the degree of knowledge and experience they possess to support, perform, and/or supervise CGMP operations. A MFG Associate III is a person with sufficient and demonstrated skills, knowledge, and experience at process Unit of Operations in a CGMP environment, while the MFG Associate I requires just the proven and correct background education. | 11/4/2022 |
| 5839 | Alcami Morrisville, NC Associate Scientist I, Micro/Environmental Monitoring Bachelor’s degree in Microbiology or similar field Exp: no related experience required |
The Associate Scientist I is accountable for driving results in a fast-paced environment by performing complex microbial analysis and assisting with method development and validation. The Associate Scientist I may assist in GMP review, provide problem solving support and Laboratory Investigation Report ownership for the Microbiology Department. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 11/4/2022 |
| 5840 | NantKwest Culver City, CA Research Associate Research Associate Research Associate B.S. in biochemistry or in related scientific disciplines Exp: up to 2 years |
ImmunityBio Inc. is seeking a highly motivated, full-time research associate to join the Protein Science group to support the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate should have a bachelor’s degree with 1-2 years of wet-lab experiences, ability to manage multiple tasks in a timely manner, good written/verbal communication skills and have a willingness to work as part of the team. | 10/25/2022 |
| 5841 | NJ Biopharmaceuticals Princeton, NJ Associate Scientist B.S. in Chemistry Exp: 0-5 years’ |
Under department supervision, plan, setup, monitor and workup chemical reactions and isolate product; optimize reaction conditions for improved yields and outputs; purify compounds by different methods; characterize and identify compounds using MS and NMR; maintain a detailed lab notebook; carry out literature searches and mine information for ongoing work from search engines; maintain equipment, chemical inventory, and provide lab support; run multiple reactions daily and provide data in a detailed report; Plan and execute daily and weekly schedule; perform safe lab practices; comply with Site safety protocols and Site Standard Operating Procedures (SOPs). Perform duties as required | 10/25/2022 |
| 5842 | NJ Biopharmaceuticals Princeton, NJ Associate Scientist/Senior Associate Scientist B.S. in Biochemistry, Protein Chemistry, or other related fields Exp: 0-5 years’ |
Under department supervision, plan, setup, monitor and purify bioconjugation reaction using aseptic techniques; characterize and identify bioconjugates using LC-MS, HPLC and/or Capillary Electrophoresis; maintain a detailed lab notebook; maintain equipment, and provide lab support; provide data in a detailed report; Plan and execute daily and weekly schedule; perform safe lab practices; comply with Site safety protocols and Site Standard Operating Procedures (SOPs). Perform additional duties as required. | 10/25/2022 |
| 5843 | NJ Biopharmaceuticals Princeton, NJ QC Scientist (I, II, III, IV, Senior, Principal) BS, MS, or PhD degree in chemistry, biology, biochemistry, or related discipline. Exp: 0-10 years |
Perform all work in a safe and compliant manner in accordance with EHS best practices and cGMP guidelines. Work with management and vendors to acquire, install, and qualify new equipment. Maintain, clean, calibrate, troubleshoot, and repair analytical instruments and equipment. Develop and execute analytical methods for small molecules, proteins, and antibody drug conjugates. Analysis of raw materials, in-process samples, finished products and stability samples by various analytical instruments and document the results under GMP settings. Prepare standard operating procedures (SOPs), analytical test methods, protocols, reports, etc. as needed. Conduct OOS, risk assessment, and root cause investigations and/or assist management with these investigations. Write deviations, change controls, and CAPAs, and/or assist management with these documents. Document work in laboratory notebooks and logbooks according to organizational GDP policies. Write, review, and execute of analytical protocols & reports for method transfers, qualification, and validations in GMP setting. Manage work outsourced to third-party analytical and metrology service providers. | 10/25/2022 |
| 5844 | Oakwood Labs Oakwood Villiage, OH Chemist Bachelor’s degree in chemistry, biology, or related discipline Exp: entry level |
This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development. | 10/26/2022 |
| 5845 | Oakwood Labs Oakwood Villiage, OH Chemical Engineer/ Biomedical Engineer Bachelor of Science, Masters, or PhD Degree in Biomedical or Chemical Engineering, or Chemistry or closely related science field with chemistry and ma Exp: entry-level |
This is an excellent entry-level opportunity for those interested in working at a technology-based pharmaceutical company. | 10/26/2022 |
| 5846 | Ocugen Malvern, PA Associate Research Scientist, Drug Substance Development Masters in Pharmaceutical Sciences, Molecular Biology, Chemistry, Biochemical engineering or in a related life-sciences field or related disciplines Exp: + 1 year |
Key responsibilities for this role include supporting the cell therapy manufacturing process, production of recombinant protein, and AAV expression in mammalian host systems. You will support the Upstream process (USP) and downstream process (DSP) scale-up to support early and late-stage projects. You will support Process Development of the pipeline projects for pre-clinical and clinical applications, allowing for Tech transfer and scale-up at CDMO partners. Ocugen’s pipeline consists of biological and gene therapy products of varying modalities which include Adenovirus assets for Vaccines, AAV for gene therapies and regenerative medicine asset for knee cartilage repair | 10/26/2022 |
| 5847 | Ortho Dermatologics Bothell, WA Quality Assurance Specialist I (WA) Quality Assurance Specialist I (WA) Quality Assurance Specialist I (WA) 4 years bachelor level degree in Science, engineering or other similar discipline. Exp: 1-3 years |
The Quality Assurance Specialist I will perform complaint investigation activities for product complaints and Adverse Events with cross functional team members and provide complaint investigation reports in compliance with Solta procedures, Food and Drug Administration (FDA), International Standards Organization (ISO), Quality System requirements, and other regulatory guidelines. | 10/26/2022 |
| 5848 | Pacific BioLabs Hercules, CA Microbiology Laboratory Analyst I/II An undergraduate or AA degree in a science-related field (e.g., Microbiology, Biological Sciences). Exp: 0-3 years |
PBL has immediate openings for full or part time Microbiology Laboratory Analysts in the Microbiology Services Department. The Microbiology Laboratory Analyst will report to Microbiology Management and will contribute to general laboratory testing, sample management, and laboratory maintenance. The Microbiology Laboratory Analyst is expected to participate with the team to meet Microbiology Services Department goals and perform routine laboratory duties as directed. | 10/26/2022 |
| 5849 | Patheon Florence, SC Scientist I - Process R&D BS/BA degree in chemistry or BS in science Exp: 0-3 years |
This is an entry-level opportunity to support the Process R&D efforts at the Florence, SC facility. | 10/27/2022 |
| 5850 | Patheon Florence, SC QC Scientist I Bachelor's degree in physical science, preferably in a life science discipline Chemistry or Biology. Exp: 0-2 years |
Provides analyses in an analytical chemistry environment within defined procedures and practices. Performs analytical methods for moderately sophisticated testing on raw materials, in-process samples, stability, and final release for APIs. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results; recommends solutions. | 10/27/2022 |
| 5851 | Patheon Cambridge, MA QC Scientist I Bachelors degree B.S. in Chemical Engineering, Biochemistry, Biology or related field Exp: 1-2 years |
Position is Sunday-Wednesday 7:30 AM to 6:00 PM. The QC Scientist I will perform routine environmental monitoring, critical utility testing, and microbiological assays. Completes method suitability testing and writes final reports. The incumbent will act as a leader in the lab helping management to interview and train junior employees, schedule testing, troubleshoot assays and equipment, and act as a SME during internal and external audits. | 10/27/2022 |
| 5852 | Patheon Cambridge, MA QC Scientist I Bachelor’s degree B.S. in Chem Eng, Biochemistry, Biology, or related field Exp: 1-2 years |
Position is Wednesday-Saturday 9:00 pm-8:30 am. The QC Scientist I will perform routine environmental monitoring, critical utility testing, and microbiological assays. Completes method suitability testing and writes final reports. The incumbent will act as a leader in the lab helping management to interview and train junior employees, schedule testing, troubleshoot assays and equipment, and act as a SME during internal and external audits. | 10/27/2022 |
| 5853 | Patheon Cambridge, MA QC Scientist I Bachelors degree B.S. in Chem Eng, Biochemistry, Biology or related field Exp: 1-2 years |
Position is Sunday-Wednesday 9:30 PM-8:00 AM. The QC Scientist I will perform routine environmental monitoring, critical utility testing, and microbiological assays. Completes method suitability testing and writes final reports. The incumbent will act as a leader in the lab helping management to interview and train junior employees, schedule testing, troubleshoot assays and equipment, and act as a SME during internal and external audits. | 10/27/2022 |
| 5854 | Patheon San Diego, CA Scientist I, Manufacturing Sciences Bachelor’s degree, in Molecular Biology, Biology, Biochemistry, Chemistry or Material Science Exp: 1+ years |
The Scientist I will support within the Technical Operations Organization in the in vitro medical diagnostics device manufacturing setting. The ideal candidate will execute experiments to support in-process assay development, process improvement with the goal of increasing product quality, consistency, and yield. Typically, this team is focused on experimental, QC, and field data for analysis, trending, and translation into root cause analysis. | 10/27/2022 |
| 5855 | Eurofins Lancaster Laboratories New Berlin, WI Chemist I Bachelor's degree in chemistry or related field Exp: 1-2 years |
Eurofins is searching for a Chemist I in New Berlin, WI. The Chemist I receives sufficient authority from, and is accountable to, the Environmental Lab Supervisor or Monograph Team Lead, or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position and to identify the occurrence of departures from the quality system or from the procedures for performing tests and/or calibrations, so long as such action does not deviate from established company guidelines, is consistent with sound technical and business judgment, and follows the practices of the laboratory. | 10/27/2022 |
| 5856 | Pliant Therapeutics South San Francisco, CA Research Associate/ Sr. Research Associate, DMPK Research Associate/ Sr. Research Associate, DMPK BS/MS degree in biochemistry, pharmaceutical science, or related scientific discipline Exp: 1-4 years |
Pliant Therapeutics seeks a highly motivated, team-oriented, and importantly, scientifically curious individual for the position of Senior Research Associated in the department of Drug Metabolism and Pharmacokinetics. The successful candidate will be responsible for conducting routine and custom in vitro ADME assays, with emphasis on permeability and transporter related assays, leveraging a solid experience in LC-MS/MS bioanalytical techniques to support drug discovery and development programs. | 10/27/2022 |
| 5857 | Pliant Therapeutics South San Francisco, CA Research Associate Scientist II, Biochemistry and High Throughput Screening BS or MS, in Biochemistry, Cellular Biology or related field Exp: One to three years’ |
Immediate opening available for Biologist/High Throughput Screening Research Associate Scientist. This individual will join a dynamic and growing multidisciplinary team focused on discovery and advancement of new drug candidates and disease biomarkers. The successful candidate will work under the direct supervision of a Senior Scientist or Scientist. | 10/27/2022 |
| 5858 | PolyPeptide Group San Diego, CA Production Chemist I BS in Chemistry, Biochemistry, Biology or related field Exp: 1+ years |
Checks reactor system for proper operation in accordance with SOP and/or operation manual. Under general supervision and direction, measures and mixes ingredients according to the BPR (Batch Production Record). Dispensing of raw materials from Pharmastore for Synthesis. During processing, monitors chemical reactions (color and completeness of chemical reactions) and under general direction of supervision and/or senior Production Chemist personnel responds with appropriate actions to ensure proper processing. Using established procedures (safety and process) and under general supervision, performs intermediate chemical processing steps. | 10/27/2022 |
| 5859 | Poseida Therapeutics San Diego, CA Research Associate, Immuno-Oncology Master's or Bachelor's degree in a Scientific discipline Exp: up to 2 years |
Poseida is seeking an outstanding candidate to join our immuno-oncology team. The Research Associate will support the development of chimeric antigen receptor (CAR-T) cellular therapies against cancer and will be involved in bench work, laboratory studies, and the coordination of research projects with the assistance of their manager or a senior lab member. | 10/27/2022 |
| 5860 | Poseida Therapeutics San Diego, CA Research Associate - Immuno-Oncology (CAR-T) BS in in the field of immunology, molecular biology, or related field Exp: 0-plus years |
Poseida is seeking an outstanding candidate to join our Immuno-Oncology team. The Research Associate will support the development chimeric antigen receptors (CAR-T) cellular therapies against cancer, and possibly other disease areas. Primary responsibilities will involve isolation of primary lymphocytes for pre-clinical research and coordination of blood product, and other raw material, inventory, characterization, and testing. Additional responsibilities may include designing and performing experiments, organizing and sharing data, and the coordination of research projects in a highly collaborative team setting, with the assistance of your manager | 10/27/2022 |
| 5861 | Poseida Therapeutics San Diego, CA Research Associate/Senior Research Associate, Gene-edited T Cell Therapies Research Associate I: Master's or Bachelor's degree in a Scientific discipline Exp: 0-2 years |
Poseida is seeking an exceptional Research Associate or Senior Research Associate to join our Immuno-Oncology team. The position will utilize NGS and other molecular biology techniques for rigorous molecular characterization of allogeneic CAR-T cells generated using Poseida’s proprietary and highly specific Cas-CLOVER gene-editing system. This position will support the Immuno-Oncology CAR-T cell therapy pipeline as well as other gene-editing platform improvement efforts. Primary responsibilities will include designing and performing experiments, organizing and sharing data, and coordinating research projects in a highly collaborative team setting. The ideal candidate will be highly motivated, detail oriented, and possess a high level of scientific rigor.\ | 10/27/2022 |
| 5862 | Poseida Therapeutics San Diego, CA Research Associate/Research Associate II, In Vivo Gene Therapy BS/MS in the field of biochemistry, molecular biology, biology or related field Exp: 6 months plus years |
Poseida Therapeutics is seeking a talented and self-motivated research associate to join our In Vivo Gene Therapy team. This position offers an excellent opportunity for a team-oriented, independent individual to assist in the pre-clinical development of novel in vivo gene therapies. | 10/27/2022 |
| 5863 | Prominex San Diego, CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
Prominex Inc. is a startup molecular diagnostic company with an experienced team of passionate and energetic scientists driven to create fast and affordable molecular diagnostic solutions across the globe. We are focused on infectious disease assays in point-of-care and home-based settings. We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 10/27/2022 |
| 5864 | Rakuten Medical San Diego, CA Research Associate I, Upstream BS/MS Exp: >1 years |
Rakuten Medical is currently looking for a highly motivated individual to support cell line and upstream process development activities. This candidate will join Rakuten Medical ’s CMC team focusing on various aspects of preclinical antibody development including transfection and single cell cloning, cell culture process development, late-stage characterization, technology transfer and research material generation. | 10/28/2022 |
| 5865 | Metrics Contract Services Toronto, ON, CA Design Engineer Bachelor’s Degree in Engineering Exp: 1-2 years |
As a Design Engineer on our Product Development Team, you'll collaborate with other engineers and work cross-functionally with our Marketing, Regulatory, Manufacturing, and Quality teams to create and modify designs for surgical instruments for spinal and cranial navigation. This is a great way for you to leverage your engineering degree to gain experience in design feasibility, testing, engineering analysis, design control documentation, and design for manufacturing. You’ll have the opportunity to tackle projects where you can provide solutions to a variety of technical problems related to complex spine products that ultimately impact patients’ lives. | 10/28/2022 |
| 5866 | Metrics Contract Services Carlsbad, CA Quality Engineer Quality Engineer Bachelor’s Degree in Engineering, Science, or related field Exp: 1 year |
The position is responsible for overseeing Quality Engineering activities related to product development and existing product support. The sustaining Quality Engineer approves Quality System documentation, provides technical support to the QC department, participates in improvement projects and CAPAs, and assists in managing external audits. | 10/28/2022 |
| 5867 | Resilience Alachua, FL Specialist, Biomanufacturing (Recent Grad) B.S. (Biology, Microbiology, Chemistry or equivalent) Exp: 0 - 2 years |
This position will assist in production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). | 10/28/2022 |
| 5868 | Resilience Alameda, CA Research Associate II, Bioanalytical Research Associate II, Bioanalytical BA/BS or MS in Biological Sciences Exp: 1-2 year |
The Research Associate II, Bioanalytical will be responsible for assisting in the development and validation of Ligand-Binding Assays (LBA) for pharmacokinetic (PK), toxicokinetic (TK), biomarkers (PD) and anti-drug antibodies (ADA) and to support sample testing for nonclinical GLP and clinical studies. | 10/28/2022 |
| 5869 | Resilience Alachua, FL Research Associate I-II Research Associate I-II BS degree in microbiology, biology, molecular biology, biochemistry, chemistry. M.S. in same areas. Exp: 0-3 years |
The research associate reports to the Associate Director or Senior Manager of Biologics and performs method development, product and process development, scale up/scale down processing, and performing a wide variety of activities including but not limited to the following responsibilities. | 10/28/2022 |
| 5870 | Resilience Alachua, FL Research Associate I-II Research Associate I-II Research Associate I BS degree in microbiology, biology, molecular biology, biochemistry, chemistry, or related field. M.S. in same areas. Exp: 0-3 years |
The research associate reports to a Senior Scientist of Vaccines and Gene Therapy and performs method development, product and process development, scale up/scale down processing, and performing a wide variety of activities including but not limited to the following responsibilities. | 10/28/2022 |
| 5871 | Resilience East Norriton, PA Manufacturing Technician II Associates/Bachelor’s (science preferred) degree Exp: 1-3 years |
The Technician II, Cell Therapy Manufacturing position is responsible for the hands-on clinical manufacturing of cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development and report to the Bioprocess and Cell Therapy Supervisor. | 10/28/2022 |
| 5872 | Resilience East Norriton, PA Manufacturing Technician I Associates/Bachelor’s (science preferred) degree Exp: 0-2 years |
The Technician I, Cell Therapy Manufacturing position is responsible for the hands-on clinical manufacturing of cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development and report to the Bioprocess and Cell Therapy Supervisor. | 10/28/2022 |
| 5873 | Rocket Pharmaceuticals Cranbury, NJ Entry Level - Clinical Manufacturing Associate I - Upstream B.A./B.S. in Life Science, Biotechnology, ChemE, or similar relevant field Exp: 0 to 2 years’ |
As a Clinical Manufacturing Associate I, you will be part of a team responsible for the start-up of a cleanroom facility and the cGMP manufacture of viral vector therapies for use in clinical trials. Additional responsibilities include set-up, operation, and cleaning of equipment, equipment, and process monitoring and troubleshooting, receiving materials and supplies from the warehouse, maintaining supply inventories, creating technical documents, and maintaining cleanrooms and equipment in an inspection-ready state. The ideal candidate will also have a strong passion and curiosity for science and gene therapy with the desire to contribute individually and collectively in a dynamic, fast-paced environment. | 10/28/2022 |
| 5874 | Rockland Immunochemicals Pottstown, PA Scientist I - Recombinant Antibodies Bachelor's or Master’s Degree in Molecular Biology, Immunology, Biological sciences or other related degree Exp: 0– 2 Years |
Rockland Immunochemicals is seeking to hire a highly motivated scientist to join our R&D team. This position of Associate Scientist or Scientist I is to participate in all aspects of recombinant antibody discovery including but not limited to primers design, antibody library construction, antibody sequence analysis, cloning, expression and purification, screening. ALL candidates with background in life sciences or related field are encouraged to apply. Training will be provided accordingly. | 10/28/2022 |
| 5875 | SCA Pharma Windsor, CT Microbiology Analyst I -2nd Shift 4 year college degree or equivalent laboratory experience Exp: 0-2 years |
At SCA Pharma, we prepare intravenous medications to be given to patients in hospitals and other healthcare facilities. Our Microbiology lab plays a key role in ensuring the sterily of our facilities and our products, to ensure that only the safest medications leave our facility. As a Microbiology Analyst I, you will be responsible for supporting the Microbiology Department with data processing/entry, Environmental Microbiological testing and Filtration Testing, in addition to daily housekeeping of the laboratory. | 10/28/2022 |
| 5876 | Serotiny South San Francisco, CA Research Associate/Senior Research Associate Degree in molecular biology, cell biology, immunology, biotechnology or related area Exp: Research Associate: BSc. with 0-3 years |
Serotiny is looking for a RA/SRA who is excited to work closely with a team of protein engineers and cell biologists to build out and deploy Serotiny's high-throughput methods to characterize and develop cutting edge therapies. We are looking for a candidate eager to contribute towards the development of a novel platform to generate and characterize CAR T cells for solid tumor indications. | 10/28/2022 |
| 5877 | Sherlock Biosciences Watertown, MA Research Associate BS in Biology, Biochemistry, Bioengineering, or related discipline. Exp: 0-2+ years |
The Research Associate will work closely with our Scientists to develop, conduct, and analyze biochemical and molecular biology experiments to support our CRISPR and Synthetic Biology-based platforms for molecular diagnostics. | 10/28/2022 |
| 5878 | SmartPharm Therapeutics San Diego, CA Research Associate/Senior Research Associate-CAR-T/CAR-NK Bachelor’s degree with relevant experience in Immunology, Molecular Biology or related disciplines. Master’s degree a plus. Exp: 1+ Years |
Sorrento Therapeutics (“Sorrento”) is seeking an experienced Research Associate or Senior Research Associate that has knowledge and hands on experience in gene editing, cell culture, Flow Cytometry and cell-based assays. This position will be responsible for the development and implementation of in vitro studies to support pre-clinical validation of CAR-T/CAR-NK cellular therapies against human cancers. | 10/28/2022 |
| 5879 | SmartPharm Therapeutics San Diego, CA Research Associate Bachelor's Degree in Life Sciences or a related field. Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking a Research Associate who, under close supervision assists in conducting laboratory experiments, maintain laboratory environment, organizing data, and analyzing results. Major tasks include: antibody discovery by phage display, antibody expression and purification, antibody characterization, cell culture and cell based assay | 10/28/2022 |
| 5880 | IQVIA Ithaca, NY Lab Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree required Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 10/18/2022 |
| 5881 | IQVIA Austin, TX Lab Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 10/18/2022 |
| 5882 | IQVIA Atlanta, GA Lab Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 10/18/2022 |
| 5883 | IQVIA Durham, NC Associate Scientist, Lab Ops Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required Exp: 6 months |
Responsible for performing routine analysis and laboratory testing procedures to obtain data for use in drug development and clinical trials research. | 10/18/2022 |
| 5884 | IQVIA Ithaca, NY Scientist, Lab Operations Bachelor’s Degree, Chemistry and/or Biology preferred Exp: 1 year’s |
The Scientist Core LC/MS (Liquid Chromatography/Mass Spectrometry) employs liquid chromatographic separation techniques and mass spectrometric analysis for data collection. In addition to instrument operation, the Scientist LC/MS is responsible for some associated instrument maintenance, documentation in accordance with SOPs and regulations, and data processing in a manner which meets company quality best practices, objectives, and timelines. | 10/18/2022 |
| 5885 | IQVIA Indianapolis, IN Associate Scientist, ADME Sciences Bachelor’s degree in relevant scientific discipline Exp: 6 months |
Responsible for performing routine analysis and laboratory testing procedures to obtain data from pre-clinical and/or clinical specimens. Provides routine documentation and review of work performed in a timely manner. | 10/18/2022 |
| 5886 | Perrigo Covington, OH QC Chemist II Bachelor of Science degree in a scientific discipline (Chemistry or Food Science preferred, Biology) required Exp: 1-2 years' |
We are currently looking for a highly motivated QC Chemist who will work 3rd shift on a rotating 2/2/3 schedule. This position pays a 10% shift premium. | 10/18/2022 |
| 5887 | Perrigo Georgia, VT Instrument Lab Analyst (2nd Shift) 4-year college degree in Chemistry or a related science is required. Exp: 1-2 years |
Perrigo Nutritionals, located in Georgia, VT, is looking for an Instrument Lab Analyst to join their team. This is a 2nd shift position running Tuesday-Saturday, 4PM-12:30AM. | 10/18/2022 |
| 5888 | Perrigo Allegan, MI Assistant/Associate/Scientist AR&D Bachelor’s OR Master's Degree in Chemistry or Pharmaceutical Sciences Exp: BS: 0-4 years; MS: 0-2 years |
Our focus is on the development of analytical methods for small molecules in support of research and characterization of new and reformulated drug products. Chief techniques include HPLC/UPLC-UV stability-indicating methods with various separation chemistries. Alternate detection methods such as ELSD and RI may also be employed along with introduction of various new analytical technologies as needed. The individual will be responsible for development of assay, impurities, dissolution, water content, and physical characterization methods for liquid and solid oral drug products. There is an expectation of both direct hands-on laboratory work as well as, depending on level of experience, mentoring/training of colleagues. | 10/18/2022 |
| 5889 | MEDTOX Baltimore, MD Research Associate Bachelor’s Degree Exp: 0-2 year |
We are currently seeking an extraordinary, highly motivated individual to join our Research and Development team, with a focus on development and evaluation of emerging technologies for tissue and cell-free DNA liquid biopsy approaches. The successful candidate will assess and optimize laboratory-based diagnostic analyses for research and clinical use following guidelines of regulatory agencies for academic, biotechnology, and pharmaceutical clients. | 10/18/2022 |
| 5890 | Merck Kenilworth, NJ Associate Scientist B.S. or M.S. degree in Chemical/ Biochemical/ Biomedical Engineering, Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Sciences, Chemistry, Bio Exp: 0-2 years |
The successful candidate will be a passionate scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible for supporting the formulation development of new biological/ chemical entities as part of a matrix team from initial first in human formulations to commercialization. | 10/18/2022 |
| 5891 | PerkinElmer San Diego, CA Quality Control Associate - Tissue Culture Bachelor’s Degree in Science Exp: 1+ year |
QC Flow Associates focused on cell & tissue culture are highly motivated team members that will primarily be responsible for the preparation of primary cells and the culture of various cell lines, as well as the set up of cell stimulations needed for flow cytometry testing of BioLegend products such as antibodies, protein reagents, buffers for immunology and related research fields. In addition, the employee may perform surface, intracellular, and multicolor testing and analysis. Primary responsibilities include performing experiments (e.g. cell culture, cell preparation and flow cytometry testing); production and analysis of reliable, reportable data; maintaining accurate documentation, utilization of internal company databases for product filing and retrieval; following company SOPs and ISO requirements. | 10/18/2022 |
| 5892 | PerkinElmer San Diego, CA Biochemist - Immunoassay - ELISA BS/BA in Biology, Chemistry, or other life science-related field. Exp: 1 year or more |
BioLegend is seeking a highly motivated Manufacturing Associate to join the Biomarker Immunoassay team in San Diego. The Manufacturing Associate will work closely with team members to ensure the timely manufacturing of high quality immunoassay products under ISO13485 standards. The Manufacturing Associate will be working closely with others in the team to ensure timely manufacturing of high-quality immunoassay products under ISO13485 standards. This role will be responsible for all aspects of product manufacturing including planning/scheduling, making and testing immunoassay components and kits, troubleshooting issues associated with product quality, and documenting and reviewing production batch records to ensure accuracy and completeness. Additional responsibilities include working with the Product Development team to ensure proper transfer of new products from Product Development to Manufacturing, filling daily immunoassay kit orders from inventoried components, and making and testing custom products in a timely manner. | 10/19/2022 |
| 5893 | PerkinElmer San Diego, CA Biochemist - Immunoassay - ELISA BS/BA in Biology, Chemistry, or other life science-related field. Exp: 1 year or more |
BioLegend is seeking a highly motivated Manufacturing Associate to join the Biomarker Immunoassay team in San Diego. The Manufacturing Associate will work closely with team members to ensure the timely manufacturing of high quality immunoassay products under ISO13485 standards. The Manufacturing Associate will be working closely with others in the team to ensure timely manufacturing of high-quality immunoassay products under ISO13485 standards. This role will be responsible for all aspects of product manufacturing including planning/scheduling, making and testing immunoassay components and kits, troubleshooting issues associated with product quality, and documenting and reviewing production batch records to ensure accuracy and completeness. Additional responsibilities include working with the Product Development team to ensure proper transfer of new products from Product Development to Manufacturing, filling daily immunoassay kit orders from inventoried components, and making and testing custom products in a timely manner. | 10/19/2022 |
| 5894 | PerkinElmer San Diego, CA Biochemist - Biomarker and Immunoassay Group (LEGENDplex™) Biochemist - Biomarker and Immunoassay Group (LEGENDplex™) Biochemist - Biomarker and Immun Bachelor’s Degree in a Biology, Chemistry, or other related field Exp: 0-2 years |
The Manufacturing Associate for the LEGENDplex™ Group will be responsible for all aspects of product manufacturing, including planning, making and testing immunoassay components and kits, trouble-shooting issues associated with product quality, and documenting and reviewing production batch records to ensure accuracy and completeness. Additional responsibilities include working with the Product Development team to ensure proper transfer of new products from the Product Development Group to Manufacturing. | 10/19/2022 |
| 5895 | PerkinElmer San Diego, CA Biochemist - GMP Bachelor’s degree Exp: 1-year |
This position is responsible for different stages of manufacturing of various BioLegend’s regulated product produced in our US FDA registered cGMP manufacturing facility. The candidate will be responsible for formulating, filling, capping, labeling, completing batch records, putting away finished good inventory (FGI), data entry, equipment maintenance and supply inspections & storage. Other responsibilities include purification of monoclonal antibodies derived from tissue culture material through an AKTA system. As well as the conjugation of purified antibody through the AKTA system. Buffer preparation and inspection of incoming buffers into the GMP suite will also be performed. Another part of the job responsibility includes preparing product/project related documentation and maintaining the device history records for all the regulated products. Working closely with product development on new products in order to establish a smooth transition into manufacturing will also be required. The desired candidate must be a team-player who is organized and has strong verbal and written communication skills and is able to work in a very fast paced environment. Great attention to detail is also a skill that will allow the candidate to be successful. The candidate must also be able to work independently and meet deadlines. | 10/19/2022 |
| 5896 | Sanofi Framingham, MA Quality Control Analyst I Bachelor’s Degree Exp: 0-2 Years |
Shift Schedule: Sunday-Wednesday shift, 12:00 pm - 10:30 pm. This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs and relevant procedures for method development, qualification, validation, method transfer, product release, stability, and process validation and investigations. | 10/20/2022 |
| 5897 | Sanofi Chattanooga, TN Quality Control Lab Chemist I Bachelor’s degree in Chemistry or related field. Exp: Zero to three years |
Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. | 10/20/2022 |
| 5898 | Sanofi Framingham, MA Manufacturing Technician Bachelor’s degree Exp: 1-2 years |
**12 hour rotating SHIFT** This position is responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 10/20/2022 |
| 5899 | Sanofi Framingham, MA Senior Manufacturing Technician Bachelor’s degree Exp: no prior experience |
**12-hour rotating day shift position including rotating holidays and weekends and overtime as per business needs** **Great promotion opportunity to build leadership skills** **Cell Experience preferred** Position in a cGMP biologics facility which includes small scale and large scale upstream operations. Initial job responsibilities will include performing a diverse range of manufacturing related activities. The Manufacturing Associate will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 10/20/2022 |
| 5900 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelors degree in Life Sciences or other relevant field of study. Exp: no prior manufacturing experience necessary |
This a third shift position. Must be able to work weekends and holidays as needed. Performs production in accordance with volume fluctuation, business need and effective procedures. Responsible for Manufacturing activities in assigned area. Identifies all production issues and relays them to the leadership team. Works to prepare assigned areas for the oncoming shifts. Completes tasks and corresponding documentation as required by cGMP. Position includes responsibilities to hand pack, operate machinery, change over duties, and clean-up functions, to assure a smooth transition between product lines. Works with Senior Technicians and Managers to ensure a smooth operation. Works to become trained in all assigned training modules. Trains and orients new team members (at any level) as assigned. Follows all procedures put into effect to ensure your safety as well as the safety of others. | 10/20/2022 |
| 5901 | Sanofi Swiftwater, PA Production Technician LL2 - Vaccine Bachelors Exp: 0+ yrs |
Performs production in accordance with volume fluctuation, business need, and effective procedures. Responsible for Manufacturing activities in assigned area. Identifies all production issues and relays them to the leadership team. Works to prepare assigned areas for the oncoming shifts. Completes tasks and corresponding documentation as required by cGMP. Position includes responsibilities to hand pack, operate machinery, change over duties, and clean-up functions, to assure a smooth transition between product lines. Works with Senior Technicians and Managers to ensure a smooth operation. Works to become trained in all assigned training modules. | 10/20/2022 |
| 5902 | Invitrogen Carlsbad, CA Antibodies QC Scientist I Bachelor of Science degree in Biology, Cell Biology, or life science related field Exp: 0-3 years |
As Manufacturing Scientist I, this individual will assure that work is performed in accordance with production schedules, perform hands-on manufacturing tasks and work in a fast-paced manufacturing environment, conduct multiple production runs at one time, and be well organized. | 10/20/2022 |
| 5903 | Invitrogen Rockville, MD Lab Technician I BS in a Biological Science Exp: 1 yr. |
The Laboratory Technician will assist in manual and automated laboratory processing of biological materials, including aliquoting and sample preparation. Tuesday-Saturday shift. | 10/20/2022 |
| 5904 | Invitrogen West Hills, CA Scientist I, Technical Operations Bachelor’s degree in Biology, Chemistry, or other similar Life Science field required Exp: 0-2 years |
The Scientist I position requires the ability to write equipment validation protocols, execute validations, and write reports for equipment. Assessing new materials requires the capability to perform risk-based comparisons of new materials to material specification documents. | 10/20/2022 |
| 5905 | Invitrogen West Hills, CA Scientist I, Manufacturing Sciences Bachelor’s degree in Biological Sciences, Biochemistry, Chemistry, Molecular Biology or related field. Exp: 0+ years |
The Scientist I, Manufacturing Sciences is responsible to lead, perform, and prioritize assigned projects related to development, improvement, production, and QC of antibody detection reagents with supervision. | 10/20/2022 |
| 5906 | Invitrogen St. Louis, MO Scientist I, QC Microbiology Bachelor’s degree required in a scientific field, preferably a Microbiology or Biology. Exp: 0 - 2 |
Provide routine analyses in microbiology by following standard practices. Perform microbiological testing of in-process samples, raw materials, buffers, media, etc. per compendial methods. Support internal development and/or manufacturing operations. Make detailed observations and reviews, documents, and communicate test results. | 10/20/2022 |
| 5907 | Invitrogen Carlsbad, CA Scientist I, Process Development Bachelors in Life Sciences, Engineering, Biochemistry, Biology or related field Exp: 1+ years |
In this role you will work alongside clients to design, develop and optimize processes that produce Plasmids for CGT and/or mRNA vaccines These Plasmids are used to treat or cure patients of life threating diseases. | 10/20/2022 |
| 5908 | Jordi Labs Mansfield, MA Chemist Master’s degree in chemistry or other closely related field. Exp: one year |
Job duties: 1) Prepare technical reports 2) Interpret gas chromatograph mass spectrometry (GCMS) and liquid chromatograph mass spectrometry (LCMS) results with a high level of proficiency 3) Interpret chromatographic data including high performance liquid chromatography (HPLC), gas chromatography (GC), and gel permeation chromatography (GPC) results 4) Combine results from multiple techniques to identify unknown chemical compounds 5) Quantify chemical components using HPLC and GC results 6) Work with a team of scientists to design and implement analytical strategies 7) Perform or oversee complex analytical strategies with an emphasis of MS and chromatography 8) Review technical reports written by other scientists | 10/20/2022 |
| 5909 | Krystal Biotech Pittsburgh, PA Research Associate, Analytical Sciences and Clinical Testing Services Bachelor’s degree (Biology, Biochemistry, Chemistry, or related science) Exp: 1-3+ years |
Krystal Biotech, Inc is seeking a highly motivated a Research Associate, Analytical Sciences and Clinical Testing Services to perform high quality analytical testing in support of Krystal’s process development and product development efforts. This position will be laboratory based. | 10/20/2022 |
| 5910 | Manifold Bio Boston, MA Research Associate / Senior Research Associate, In Vivo PharmacologyResearch Associate / Senior Research Associate, In Vivo Pharmacology Bachelors or Masters Exp: 1-2+ years |
We are seeking a highly-motivated In Vivo Pharmacology Research Associate / Senior Research Associate who thrives in a fast-paced and creative environment to push the capabilities of our multiplexed in vivo drug discovery platform. Together with senior researchers, you will play a critical role in executing in vivo studies to support internal research projects. This is a hands-on role and you should have extensive experience in multiple aspects of in vivo pharmacology including dosing, pharmacokinetic sampling, and necropsy, among others. The ideal candidate must be able to work effectively both in a collaborative setting and Independently. | 10/20/2022 |
| 5911 | Masy Bioservices St. Louis, MO Associate Scientist I, Microbiology Bachelor’s degree Biology, Microbiology or related field. Exp: 0-2 years |
The Associate Scientist, Microbiology is accountable for driving results in a fast-paced environment by accurately and efficiently performing sample analysis, monitoring microbial cultures and identifying microbiological contaminants and pathogens using a variety of identification methods. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 10/20/2022 |
| 5912 | Masy Bioservices Charleston, SC Associate Scientist I, Microbiology - 3rd Shift Bachelor’s degree in Chemistry, Biology, Microbiology or a related field. Exp: 0 – 2 + years |
The Associate Scientist I is accountable for driving results in a fast-paced environment. The position is responsible for performing monitoring of the pharmaceutical manufacturing environment and utilites in complaince with cGMP and internal SOPs. The incumbent will provide support to manufacturing and laboratory operations. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 10/20/2022 |
| 5913 | Med Institute Pittsburgh, PA Quality Control Associate I Undergraduate degree any Life Sciences, Engineering field, Microbiology, or Molecular Biology Exp: 1-3 years' |
The Quality Control Associate I at Cook MyoSite will aid in the development and maintenance of methods for sampling, testing, evaluating, and approving testing results for products and materials. | 10/20/2022 |
| 5914 | Mekonos Berkeley, CA Research Associate, Chemistry B.S or M.S in Chemistry, Chemical Engineering, Material Science, Biochemistry or a related discipline Exp: 1-3 years |
Further the development of our patented delivery chemistry Plan and execute research operations Assist with lab management tasks (procurement, inventory, equipment maintenance, etc.) Demonstrate high scientific integrity and reporting standards Promote a positive and exciting work environment | 10/20/2022 |
| 5915 | Minnetronix Medical St. Paul, MN Design Quality Engineer Bachelor’s Degree/Technical Degree in Engineering or equivalent experience Exp: 0-5 years’ |
Design Quality Assurance Engineers work with design teams to ensure that electronic and software subsystems incorporated into medical devices are designed in accordance with product requirements and the devices meet their intended use. They develop and perform verification and validation activities on medical devices and medical device systems. Verification testing may involve GUI testing, black-box system testing, environmental testing, requirements based functional testing and low-level hardware testing and fault simulation. Design QA Engineers drive quality in all project deliverables and ensure that development teams follow processes that are effective and compliant to Standard Operating Procedures. They work with both the customer and internal team members to drive successful outcomes and long-term value for both the customer and Minnetronix. Design QA Engineers may work under the direction/supervision of more senior Design QA staff members to ensure resolution of technical issues and knowledge transfer. | 10/21/2022 |
| 5916 | Minnetronix Medical St. Paul, MN Manufacturing Engineer I Bachelor’s degree in an engineering, technical or scientific disciple. Exp: 0-3 Yrs |
Manufacturing Engineer I will work cross functionally to manage the production build of complex electro-mechanical medical devices. A Manufacturing Engineer I can be responsible for the production build of multiple product lines. Their responsibilities include: production documentation, issue tracking and resolution, and continuous improvement. | 10/21/2022 |
| 5917 | Myriad-RBM Austin, TX Lab Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 10/21/2022 |
| 5918 | NAMSA Irvine, CA Associate Microbiologist Bachelor degree Exp: one year |
Independently perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs, and according to applicable work instructions. • Prepare or participate in the preparation of test specifications in conjunction with the requirements of the applicable standards and/or client instructions. • May have direct client contact as needed. | 10/21/2022 |
| 5919 | NAMSA Northwood, OH Microbiology Technologist Bachelor degree Exp: no experience |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. • Accurately collects and records raw data in logbooks and on worksheets. • May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. • May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. • May be required to operate autoclave, depyrogenation oven or other specified laboratory equipment. • May perform Kinetic-Chromogenic LAL testing. • May perform Environmental Monitoring, clean and disinfect cleanroom suites. • Other duties as assigned | 10/21/2022 |
| 5920 | Frontida BioPharm Philadelphia, PA ASSOCIATE ANALYTICAL SCIENTIST Master’s Degree Exp: 1+ years |
The Analytical Scientist II reports to the Associate Director of Analytical Research and Development and is based at our Philadelphia location. This is a laboratory-based position and the Scientist will be responsible to support formulation development by performing method development, validation, writing protocols and reports, conducting chemical and physical testing activities for both ANDA and NDA projects. | 10/11/2022 |
| 5921 | Frontida BioPharm Vandalia, OH QC ANALYST Bachelor degree in Chemistry or related field Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 10/11/2022 |
| 5922 | Frontida BioPharm Vandalia, OH QC ANALYST (NIGHT SHIFT) Bachelor degree in Chemistry or related field Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 10/11/2022 |
| 5923 | Frontier Medicine South San Francisco, CA Compound and Sample Associate I B.S. or M.S. in Chemistry, Chemical Engineering, Biology or related discipline required Exp: 0-1 year |
Frontier Medicines is seeking a highly motivated individual for a newly created Compound and Sample Associate I. The successful candidate will be accountable for the storage, retrieval, and distribution of compounds for biological assays as well as chemical building blocks for compound synthesis and QC. The position is located in South San Francisco, CA. | 10/11/2022 |
| 5924 | Frontier Medicine South San Francisco, CA Research Associate, Protein Sciences BS or MS in Biochemistry, Biological Sciences, or a related field Exp: 0-2 years |
We are seeking highly motivated research associates to join our group in South San Francisco, CA. This is an exciting opportunity for experienced and passionate associates or recent graduates to apply and expand their skills in protein sciences and contribute to the discovery of innovative therapies. The successful applicants will carry out experiments in protein expression, purification, and characterization to support biochemical assays and structure determination. Working closely with an experienced team of interdisciplinary scientists, the candidates will have regular opportunities to present findings to the Protein Sciences team. The ideal associates should have a strong desire to learn new techniques and incorporate new methodologies into their work, as well as be detail-oriented, self-motivated, well organized, and enjoy working and learning in a dynamic team environment. | 10/11/2022 |
| 5925 | Fujifilm Diosynth Mesa, AZ Process Technology Engineer BS Degree Engineering (Chemical, Mechanical or Materials Science preferred). Exp: 0 to 2 years |
The Process Technology Engineer will work with the Process Technology Group (PTG) to operate process scaling equipment, collect ultra-high purity samples from both pilot and full scale operating equipment to issue summary reports as directed by PTG’s senior engineering staff. | 10/11/2022 |
| 5926 | Fujifilm Diosynth College Station, TX Process Sciences - Associate Engineer - Material Transfer Bachelor’s/ Master’s Degree Degree in a science related field Exp: 1 year |
The Material Transfer Associate is responsible for compiling, organizing and reviewing documents that summarize safety testing results and/or describe safety characteristics of select incoming materials. They are also responsible for performing the material entry evaluation, identify gaps and perform risk analysis when needed to complete the material induction process. In addition, the Material Transfer Associate will be working with internal and external stakeholders to complete the transfer of materials from the client(s) to FDB (Fujifilm Diosynth Biotechnologies) for supporting process development work and cGMP manufacturing activities by monitoring inventory and tracking incoming materials, especially biological materials. | 10/11/2022 |
| 5927 | Fujifilm Diosynth College Station, TX QC Cell Biology Analyst II Master’s degree preferably in Biology or Biochemistry Exp: one (1) year |
The Cell Biology Analyst II will be responsible for participating in the Technology Transfer of established methods into the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. | 10/11/2022 |
| 5928 | Glypmse Cambridge, MA Research Associate/Sr. Research Associate, Chemistry high throughput screening BS or MS equivalent degree in chemistry, biochemistry, biology or relevant discipline Exp: 1-3 years |
Our Screening and Automation group is seeking a motivated Research Associate who will contribute to the development of novel diagnostics in our Chemistry platform. This person will perform work at the intersection of Chemistry, Biology and Computational Science, participating in experimental design and execution, generating data, and collaborating on analyses. The individual we hire will have the opportunity to lead screening campaigns, execute on established workflows, optimize and develop new assays, and help build out new tools and functionalities. | 10/11/2022 |
| 5929 | HemoSonics Raleigh/Durham/Chapel Hill, NC Associate Quality Engineer BA/BS degree in science, engineering or related technical field Exp: 1 - 4 years’ |
HemoSonics, LLC is seeking an Associate Quality Engineer for our Quality Assurance team. This position is responsible for providing quality engineering support to the management and maintenance of all Quality Systems elements to meet the company’s business needs, developing company best practices, standards, continuous improvement and ensuring compliance with regulatory requirements and standards. The Associate Quality Engineer works cross functionally with Operations, Supply Chain Management, R&D and internal quality groups to provide guidance on GMP and best practices. | 10/12/2022 |
| 5930 | HistoTox Labs Gaithersburg, MD Animal Study Technician I B.S. or B.A. degree in Biology, Life sciences, Chemistry or Science field Exp: 0+ years |
Learns how to review study protocol and ensure study tasks and data for pre-clinical research studies are conducted in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. Learns how to generate study forms and worksheets. Receives extensive training in various technical procedures including dose administration, sample collection, handling and restraint of multiple species. Learns to perform and document observations on study animals. Learns to record observations and collect other relevant data via data capture systems and/or hand-generated forms in accordance with GLPs, SOPs, and protocol. | 10/13/2022 |
| 5931 | HistoTox Labs Rockville, MD Associate Scientist - Biotherapeutics BSc or MSc in Immunology, molecular biology, bioanalytical chemistry, drug metabolism, pharmacokinetics, or related science Exp: 1-3 years |
The associate scientists should have knowledge and experience in ligand binding assay techniques, e.g., ELISA, MSD, Luminex, cell-based assays for PK and Immunogenicity determinations, or knowledge of PCR, DNA, RNA analysis, as well as flow cytometry. Due to the different techniques involved, some associate scientists would need essential experience in PCR, DNA, RNA, and flow cytometry analysis with a working knowledge of ligand binding assay techniques, e.g., ELISA (HELISA, etc.), MSD, Luminex, cell-based assays for PK and Immunogenicity determinations and LC-MS/MS. Depending on their experience and capabilities they will be placed in the different sections. The associate scientists of the Biotherapeutics laboratory will perform analysis of samples generated in the GLP/GCLP laboratory for preclinical samples according to the applicable FDA/EMA Guidelines. The associate scientists will thrive in a collaborative and welcoming environment that values a culture of empowerment, transparency, innovation, agility, professional growth, and credibility providing them the opportunity for promotion to scientists. | 10/13/2022 |
| 5932 | HistoTox Labs Rockville, MD Associate Scientist I (In Vitro Cytogenetics) Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 1+ years |
Perform a wide variety of in vitro assays or tests required to characterize product or material safety Maintain sterile and good cell/tissue culture techniques Prepare study reagents in accordance with SOPs and study instructions Use and maintain scientific equipment, instrumentation and computer systems Conduct pre-designed assays using basic laboratory techniques and skills Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations Perform peer review of data and lab support records | 10/13/2022 |
| 5933 | HistoTox Labs Raleigh, NC Research Assistant A.S. or B.S. in biology or related field Exp: 0-3 years |
We are expanding in our Genetic Toxicology team in our Research Triangle Park location. Our group is performing regulated toxicology studies in laboratory rodents for commercial and governmental clients. Responsibilities The Genetic Toxicology Group conducts standard and custom genetic toxicology testing and applied research supporting preclinical studies for both federal and commercial clients. | 10/13/2022 |
| 5934 | HistoTox Labs West Lafayette, IN Bio Analyst I B.S. in chemistry or biology Exp: one year |
Conducts sample analysis with data interpretation and basic troubleshooting. Conducts method development and method validation experiments. Assists with general housekeeping and assist other departmental personnel as necessary. | 10/13/2022 |
| 5935 | IFyber Ithaca, NY Laboratory Technician a BS degree Exp: 1 year (more preferred) |
The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. | 10/13/2022 |
| 5936 | IGM Biosciences Doylestown, PA Research Associate II / Research Associate III MS or equivalent in Biology, Immunology, or another related science degree Exp: RAII: MS with 0-2 years |
We are looking for a Research Associate II/III with a background in in vitro immunology assays and the development of biologics to join our growing and friendly team during this exciting time in our expansion. The successful candidate will play an integral role in developing novel autoimmune and inflammation therapeutics pre-clinical development. You will perform in vitro studies, standard immuno-assays, problem solve and constantly improve work practices and work productively as part of a team contributing to advancing innovative applications of the IgM platform for autoimmune and inflammatory disease. | 10/13/2022 |
| 5937 | IGM Biosciences Doylestown, PA Research Associate / Senior Research Associate, Drug Product Degree in Biochemistry, Chemistry, Biology, or related background. Exp: MS with 0 - 2 years |
We are hiring a Research Associate to join our rapidly growing Drug Product team in support of IGM program development. In this position you will be responsible for executing scientific research and development projects in collaboration with colleagues across business units and programs to support end-to-end Research & Development and Company goals. You will execute studies to develop frozen, liquid, dried, and novel Drug Product and develop devices to enable pre-IND and post-IND clinical requirements. You will engage with all partner groups including upstream pre-clinical discovery and Drug Substance purification through downstream manufacturing, clinical supply, operations, analytical, and regulatory colleagues internally. | 10/13/2022 |
| 5938 | IGM Biosciences Mountain View, CA Research Associate II / III, Cell Line Development BS or MS in Cell Biology, Biochemistry, or related scientific discipline. Exp: 1 – 3 years |
IGM Biosciences is hiring a Research Associate in our Cell Line Development group to join our rapidly growing team. In this position you will support the development of novel antibody products by helping to create cell lines producing these therapeutic antibodies. You will work on cell pool generation, single cell cloning, maintain and expand cells, cell banking, cell line characterization, and execute antibody production runs. | 10/13/2022 |
| 5939 | InBios International Seattle, WA Manufacturing Associate I- ELISA Bachelor’s degree with emphasis on life science Exp: 1-year |
We would like to see your resume if you have received a degree with an emphasis on life sciences. If you have work experience in a GMP/ISO 13485 manufacturing facility and/or you have experience with PCR test-kit manufacturing please be sure to include that information on your resume or in a cover letter. If you would like to be part of a team responsible for the production of large-scale ELISA diagnostic test components in a BSL-2 laboratory, and you enjoy a busy workday under general supervision with daily goals working alongside a dedicated team that consistently meets deadlines and delivers products that meet high quality standards, then we encourage you to apply for this position. | 10/13/2022 |
| 5940 | InBios International Seattle, WA Manufacturing Associate I- Rapid Spray Bachelor’s degree in life sciences or a similar field Exp: 1 year |
We are searching for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other Inbios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale lateral flow diagnostic test components. If you are seeking an entry-level position with short-term and long-term opportunities for experience and growth at the forefront of medical diagnostic biotechnology this is a great opportunity for you. | 10/13/2022 |
| 5941 | InBios International Seattle, WA Quality Assurance Associate II MS Exp: 1+ years |
We are seeking a mindful and diligent individual with a warm and welcoming attitude who has excellent organizational and communication skills and a keen eye for detail. If you enjoy analytical work, leading and collaborating on projects, a variety of responsibilities, and being part of a reliable and dedicated Quality Assurance team, then we encourage you to apply for this position. | 10/13/2022 |
| 5942 | InBios International Seattle, WA Quality Control Assistant - Biotech BS in Chemistry, Biology, Bioengineering, or other relevant discipline. Exp: 0 – 1 year |
You have a degree in chemistry, biology, bioengineering or related life science field of study and are looking for an entry level QC position and an opportunity to learn and grow your skills and career. You thrive in a busy and structured work environment working with a team of Quality Control Associates under the supervision of the Quality Control Manager. You are thorough and able to see and report details and variances as well as able to follow and adhere to established procedures and protocols. You are a reliable worker who is comfortable working and contributing to team demands and goals. | 10/13/2022 |
| 5943 | InBios International Seattle, WA Quality Control Associate I BS or MS in Bioengineering, Chemistry, Biology or other relevant discipline. Exp: 1 year |
You are looking for a new job working with a dedicated and reliable team of quality control professionals. You are a meticulous individual who thrives in an environment with demanding attention to detail; and you take pride in meeting deadlines, using your critical thinking skills, and working with your team and other teams to ensure top quality products are delivered. You have a warm and welcoming attitude and outlook as you approach each workday. If this describes you and the kind of team and work environment you are seeking, we encourage you to apply. | 10/13/2022 |
| 5944 | Instil Bio Thousand Oaks, CA Research Associate, Cell Biology MS Degree Exp: 1+ years |
We are seeking a highly motivated individual to join the research team to participate in Instil Bio’s late-stage efforts and play a pivotal role in advancing key TIL engineering programs to clinical stage. The successful candidate will be part of a research team focused on advancing current programs to IND. In this role, the candidate will initially be directly reporting to Director of Late-stage Research. | 10/13/2022 |
| 5945 | IntelliSyn R&D Waltham, MA Research Associate BS or MS in Chemistry or related subject Exp: 6 months-2 years |
X-Chem is seeking a candidate for the position of Research Associate, Library Synthesis in its Discovery Chemistry group. X-Chem is a drug discovery company that uses DNA-encoded library (DEL) technology to discover leads for therapeutic targets. As a world leader in DEL technology, X-Chem collaborates with numerous pharmaceutical and biotechnology companies, resulting in over 70 licensed programs to date. | 10/13/2022 |
| 5946 | Pace Analytical Maplewood, MN Lab Analyst - Microbiology BS degree in Biological science or related field Exp: 1-3 years |
This position will actively support food safety and quality assurance through the use, and validation of, pathogen detection products. The analyst will prepare and evaluate samples using aseptic technique to ensure products meet specifications. The products being monitored are crucial to maintaining consumer safe food supply chains. Work is performed as part of a team in a collaborative environment. | 10/13/2022 |
| 5947 | Invicro San Diego, CA Associate Scientist, Radiochemistry M.S. or B.S. Exp: 1-3 years’ |
Invicro is seeking a full-time Associate Scientist to focus on Radiochemistry. All levels of chemistry trained individuals are encouraged to apply. This role will be focused on radioisotope labeling of various small and large molecules, along with using analytical techniques to evaluate the labeled products. The radiolabeled molecules will be provided to imaging lab teammates who will carry out PET and SPECT imaging studies on rodents. Radiochemistry experience is desirable, but not required, and complete training will be provided by an experienced radiochemist. Though the radiochemistry experience is not mandatory, the ideal candidate should have knowledge in organic synthesis, product purification, and analytical chemistry. The candidate should have a strong desire to learn radiochemistry and operation of analytical equipment (full training will be provided). The candidate should be able to work independently with remote support where necessary. The role requires radiation safety training before learning radiochemistry and managing the labeling chemistry for PET and SPECT imaging projects. | 10/13/2022 |
| 5948 | Invicro Aliso Viejo, CA Laboratory Assistant, Pathology Bachelor’s degree in a relevant biological science. Exp: 1-2 years’ |
Make an impact at a dynamic and growing company! Invicro seeks a Laboratory Assistant for Advanced Pathology Services to support for all routine Histology and IHC work pertaining to delivery of CAP/CLIA and GLP-like oriented lab services offered to external partners, including BioPharma, Academia, and Oncology Research Centers. Our laboratory performs high complexity immunohistochemistry and other advanced tissue analysis approaches unique to Invicro. This individual should enjoy challenging and analytical work and be motivated by the idea that together we can accomplish great things and make a positive contribution to society through our mission. | 10/13/2022 |
| 5949 | Invicro San Diego, CA Associate Scientist, In vivo Imaging and Pharmacology BS in bioengineering, biomedical engineering, medical physics, radiologic sciences, biology, pharmacology, or other engineering degree Exp: 1-3 years |
Invicro is currently looking for an Associate Scientist to join its San Diego based lab. The candidate will execute in vivo, small animal medical imaging studies and related in vivo pharmacology procedures, including nuclear medicine (PET/SPECT), computed tomography (CT), and magnetic resonance imaging (MRI). The candidate will join a team in our multi-modal imaging laboratory and aid in the development of novel therapeutics and diagnostics. This position will provide an opportunity for rapid technical growth and exposure to cutting-edge pharmaceutical industry research projects. The successful candidate will join a close, dynamic, expanding, diverse and highly performing team. | 10/13/2022 |
| 5950 | InVivoScribe San Diego, CA Manufacturing Associate I B.S. Degree in a scientific discipline, preferred. Exp: 1+ years |
We are looking to add a Manufacturing Associate I to our team for all aspects of production, including the production of master mixes and controls. You will contribute to the drafting and review of new documents, including SOPs, Batch Records and Purchasing Specifications. | 10/13/2022 |
| 5951 | Vigene Biosciences Northridge, CA Research Associate I Bachelor’s degree in Biological Sciences required. Exp: 1 year |
This position is responsible for the evaluation of human blood products for manual or automated cell isolations, product manufacturer, and cell culture. Perform QC testing and create a certificate of analysis (COA) for products manufactured. Record isolation details on a processing worksheet using good documentation practices. Operate flow cytometer and basic lab equipment. | 10/13/2022 |
| 5952 | Vigene Biosciences Memphis, TN QC Flow Analyst 1 BS or higher degree in the biological sciences or related field Exp: 1-2 years |
Charles River Laboratory Biologics is currently seeking an Analyst 1 to perform flow cytometry for our Quality Control Department. The successful candidate will be responsible for performing routine quality control product and raw material release testing utilizing multi-color flow cytometry as well as various biochemistry, molecular biology, and general laboratory techniques according to GMP. Additionally, the analyst will assist QC Scientists with technology transfer of new client assays by Co-authoring SOPs or other required documentation. The position requires the utmost attention to detail, very strong organizational skills, computer proficiency, and a basic understanding of laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success. | 10/13/2022 |
| 5953 | Vigene Biosciences Memphis, TN Manufacturing Associate I (EG) - 4 - 10 Hour Shifts Available AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
We are seeking a Manufacturing Associate for our Cell Therapy Manufacturing Facility located in Memphis, TN. The Manufacturing Associate I is responsible for performing various manufacturing activities related to the start- up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 10/13/2022 |
| 5954 | Vigene Biosciences Memphis, TN Quality Ops Specialist I bachelor’s degree in scientific field. Exp: Zero (0) to one (1) year |
We are seeking a Quality Ops Specialist I for our Cell Therapy Manufacturing Facility located in Memphis, TN. | 10/13/2022 |
| 5955 | Vigene Biosciences Memphis, TN Quality Control - Analyst Raw Materials A.A. or B.S. degree in Chemistry, Biochemistry, Biology or related discipline is required. Exp: 0-2 years |
Charles River Biologics in Memphis is seeking applicants for the QC Raw Material Analyst I position. As a key member of our Quality Control department, the Analyst is responsible for the day to day activities covering the inspection, sampling and testing of incoming raw materials. The analyst will report into the Manager and/or Supervisor of the QC Raw Material Department. | 10/13/2022 |
| 5956 | Align Technology San Jose, CA Associate Scientist Bachelors in Chemistry or polymer chemistry or related fiele Exp: 0-2 years |
We are looking for an innovative candidate to be a key contributor as a Associate Scientist in our San Jose, CA location. As a key member of the R&D Materials Engineering team, you will be responsible for supporting on the new product development as well as improving Align's existing products. The ideal candidate will have a background in chemistry and 3D printing resin development. | 10/13/2022 |
| 5957 | Charles River Laboratories Spencerville, OH Research Technician Assistant (Entry Level) Associates or BA/BS in a life science field preferred. Exp: 0-6 months |
A Research Technician Assistant is responsible for: collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Hourly Rates $18-$19/hr. $1000 Sign on Bonus. 3 weeks vacation and additional sick time. | 10/14/2022 |
| 5958 | Charles River Laboratories Spencerville, OH Research Technician Assistant (entry level) Associates or BA/BS in a life science field preferred. Exp: 0-6 months |
A Research Technician Assistant is responsible for: collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Hourly Rates $18-$19/hr. $1000 Sign on Bonus. 3 weeks vacation and additional sick time. | 10/14/2022 |
| 5959 | Charles River Laboratories S. San Francisco, CA Research Associate I BS in the biological sciences or relevant area required. Exp: 0-3 years |
Explora BioLabs, an entity of Charles River, is seeking a Research Associate I located in San Francisco, CA. In this role, the incumbent will perform a variety of animal procedures to support company and client research projects (e.g., set up the study forms, set up the procedure rooms, label and ship samples, etc.). To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. | 10/14/2022 |
| 5960 | Stryker Portage, MI (ENTRY LEVEL)Design Engineer, Electrical Bachelor's degree in EE or related discipline Exp: 0+ years |
Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success and contribute to the project as a team member Learn procedures, policies, processes, systems, and technology required\ Work on problems in limited scope; purposefully learn while gaining experience Demonstrate ownership and integrity of work Build stable relationships | 10/4/2022 |
| 5961 | Acrotech Biotech East Windsor, NJ LABORATORY TECHNICIAN Bachelor Degree in related scientific field Exp: 1-3 years |
Microbiologist will perform a variety of Microbiology testing to assess the strength, identity and purity of test samples and/or materials. The Microbiologist will work as a member of team to effectively plan and Microbiology testing using established (official in USP and/or in-house) test procedures. The Microbiology may execute 90% - 100% of their work at the bench level. | 10/4/2022 |
| 5962 | Acrotech Biotech East Windsor, NJ MICROBIOLOGIST I Bachelor Degree in related scientific field Exp: 1-3 years |
Microbiologist will perform a variety of Microbiology testing to assess the strength, identity and purity of test samples and/or materials. The Microbiologist will work as a member of team to effectively plan and Microbiology testing using established (official in USP and/or in-house) test procedures. The Microbiology may execute 90% - 100% of their work at the bench level. | 10/4/2022 |
| 5963 | Acrotech Biotech East Windsor, NJ ASSOCIATE CHEMIST II BS with Chemistry Exp: 1-3 years |
Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 10/4/2022 |
| 5964 | Acrotech Biotech Dayton, NJ ASSOCIATE CHEMIST II (TEMP) BS with Chemistry Exp: 1-3 years |
Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 10/4/2022 |
| 5965 | Cell Signaling Technology Danvers, MA Research Associate (Monoclonal Development) Bachelors degree in cell biology or immunology preferred Exp: 1+ years |
The Research Associate is a member of the Monoclonal Development team which is a core function for antibody development at CST. This individual will be responsible for screening XMT and mouse fusions to provide monoclonal antibody clones with the best utilities possible to be developed into final products. This position will focus on an early step in our product development process and will enable broad exposure to the full monoclonal antibody development process. | 10/5/2022 |
| 5966 | Civetta Therapeutics Cambridge, MA Cell Biology Research Associate BS in Biology, Molecular Biology, Biochemistry, or related Life Science discipline Exp: 1-3 years |
We are seeking a highly-motivated Research Scientist to help support our chemical biology efforts at Civetta. This candidate will help us discover small molecule modulators of beta-propeller proteins, support validation of new targets, and help propel our ongoing drug discovery programs. This is an excellent opportunity for individuals looking to work in a fast-paced, dynamic biotech environment. | 10/5/2022 |
| 5967 | Repligen Hopkinton, MA Process Engineer Engineering degree or equivalent required Exp: 0-3 years |
We are seeking motivated and experienced process engineer who will focus on multiproduct manufacturing support, project execution, validation, and tech transfer. The position is based in Massachusetts and will be focused on Process support & development for multiple product lines within the field of bioprocessing. This individual will work closely with Manufacturing and R&D to improve current and new products. The successful candidate will play a key role in ensuring that the department's production and quality goals are met. The applicant will be the key interface between manufacturing, quality and R&D. Hands-on mechanical aptitude and an exceptional problem-solving ability are important. | 10/5/2022 |
| 5968 | Rho Durham, NC Research Associate, Federal Research Bachelor’s degree in a scientific field or a related area of study with research emphasis Exp: entry-level |
The Research Associate will assist project managers in day-to-day operations of either federally-funded or commercial studies. This is an entry-level position. This is not a laboratory research position. | 10/5/2022 |
| 5969 | WuXi Apptec San Diego, CA Research Associate II Bachelors in Life Sciences or related field. Exp: 1 to 2 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its IO in vitro Division. We are seeking a highly skilled and motivated Research Associates to help advance HD Biosciences’ immuno-oncology team to complete client-based projects and experiments. | 10/5/2022 |
| 5970 | WuXi Apptec Cranbury, NJ Associate Scientist I Bachelor's degree in chemistry or closely related physical science Exp: 0 - 3 years |
The Associate Scientist I is responsible to conduct and/or provide support for various types of in vitro ADME assays in support of discovery and development programs in the DMPK department. | 10/5/2022 |
| 5971 | WuXi Apptec Cranbury, NJ Associate Scientist II Master’s degree in animal science, biology, or a related scientific discipline. Exp: 0 -1 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC and other standards. Operates lab equipment including oxidizers, centrifuges, LS counters, cage/tunnel washers, infusion pumps, etc. | 10/5/2022 |
| 5972 | WuXi Apptec San Diego, CA Research Associate I Bachelors preferred Exp: 0-1 years’ |
We are growing and seeking a motivated Research Associate I to support our in vivo pharmacology team for various projects. | 10/5/2022 |
| 5973 | WuXi Apptec San Diego, CA Research Associate I - In Vivo Pharmacology Master degree in Molecular and Cell Biology or Bachelor degree Exp: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate I to support our in vivo pharmacology team for various projects. | 10/5/2022 |
| 5974 | WuXi Apptec San Diego, CA Research Associate II - In Vivo Pharmacology Master degree in Molecular and Cell Biology or Bachelor degree Exp: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 10/5/2022 |
| 5975 | Catamaran Bio Boston, MA Research Associate / Senior Research Associate, Cell Culture BS or certificate in biology, biotechnology, or equivalent/related disciplines. Exp: 1-5 years |
Catamaran is seeking an experienced, hands-on Research Associate / Senior Research Associate to support Catamaran’s development of an allogeneic NK cell drug product. The successful candidate will be responsible for generating and maintaining stocks of cell lines used for in vitro and in vivo assays, including feeder cells, tumor cell lines, NK cells and genetically modified cells. This work involves cell isolation, expansion, engineering, harvest and cryopreservation. This role will require collaborating extensively with Research and CMC teams. The ideal candidate has relevant experience in cell culture of primary human cells and cell lines, and is excited to join a small, fast-paced team with a “can-do” attitude to drive forward our new cell therapy platform. | 10/5/2022 |
| 5976 | Catamaran Bio Boston, MA Research Associate/Senior Research Associate, Cell Process Bachelors or master’s degree in chemical engineering, immunology, biology, synthetic biology, chemical biology, biochemistry, pharmaceutical sciences, Exp: 0-2 years’ |
The Cell Process Team is seeking a talented, diligent, and collaborative research associate to execute and design cell expansion process activities for the advancement of our best-in-class CAR-NK Cell Therapies for Oncology and other diseases. Cell Process works to ingeniously solve the challenges associated with the allogeneic manufacture of CAR-NK cell therapies including cell isolation/enrichment; cell engineering and gene editing; and cell expansion. They will be responsible for the operation of a clinical-scale bioreactor process design for the expansion of clinical CAR-NK candidates, execution of cell-based assays for in-process characterization, and technical process transfer to internal and external manufacturing sites in support of Phase 1 clinical activities. The ideal candidate is a self-motivated and technically competent process development scientist or engineer with an interest in bioreactor design and control, who is excited to join a small, fast-paced team with a “can-do” attitude to drive forward our new cell therapy platform. This is a unique opportunity to realize the promise of allogeneic cell therapy manufacturing paradigms and bring the TAILWIND platform to life at a clinical scale. | 10/5/2022 |
| 5977 | Cel-Sci Baltimore & Elkridge, MD Validation Engineer B.S. in a related discipline Exp: 1 to 5+ year |
The Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor. | 10/6/2022 |
| 5978 | Circle Pharma South San Francisco, CA Research Associate/Sr. Research Associate, Analytical Chemistry M.S. degree in Chemistry, Biology or a related scientific discipline Exp: 0+ years |
We are looking to add a Research Associate or Senior Research Associate to our growing Chemistry team. Reporting to our Director of Analytical Chemistry, this RA will be responsible for the purification and analysis of target molecules, as well as routine instrument maintenance. Our ideal candidate will have experience in small molecule/peptide purification and analysis. Our ideal candidate will also have a proven track-record of productivity and project ownership, coupled with a solid understanding of small molecule/peptide purification and analysis techniques. | 10/6/2022 |
| 5979 | Concuir Consulting Los Angeles (Hybrid), CA ASSOCIATE CONSULTANT – ENGINEER I/II Bachelors or higher in Engineering or Science Exp: 0-2+ years’ |
As a full-time employee of Concuir, Inc, you will provide consulting services to pharmaceutical, biotech and/or medical device clients. In this role, you will quickly learn client typical practices and be in a position to recommend and implement improvements to reach project goals. This is based on your experience as well as from Concuir’s portfolio of project management and cGxP best practices. Typical projects range from design through qualification of production equipment and/or utilities to modification or implementation of new facilities and process scale ups. | 10/6/2022 |
| 5980 | CorneaGen Seattle , WA Laboratory Assistant/Transporter (On-Site) B.S. degree in a life science field education is a bonus. Exp: Entry-Level |
The Laboratory Assistant/Transporter plays a vital role by ensuring packages are delivered and received on time. As a Laboratory Assistant/Transporter, you will be responsible for delivering corneal tissue to local destinations via company vehicle and retrieving packages from the airport and local hospitals. Additionally, this role supports the laboratory in our Seattle office by ordering and stocking supplies, ensuring the lab is clean, and assist with packing tissue in accordance with department protocols. On a daily basis, this position helps ensure that our customers - surgeons all across the world - are able to get what they need when they need it so that they can successfully complete their corneal transplant surgeries for their patients and help them regain their eyesight. If you're the type of individual who enjoys driving and prides yourself on driving safely, this is an opportunity to apply your skills and experience and truly make a difference in people's lives! | 10/6/2022 |
| 5981 | Cytokinetics South San Francisco, CA Research Associate, Medicinal Chemistry BS/MS in Chemistry Exp: 0-3 years |
We are currently seeking a Research Associate for our Medicinal Chemistry department. As a Research Associate, you will thrive as a highly motivated and creative scientist! This is an exciting opportunity to be part of a growing, dynamic, and highly collaborative R&D team involving novel target approaches to find medicine for unmet medical needs! Our Research Associates collaborate with scientific mentors in a one-on-one reporting structure to design and efficiently synthesize target molecules for evaluation as potential drug candidates. You will collaborate with a broad group of highly experienced scientists and focus on advancing drug discovery research programs to the stage of clinical development. | 10/6/2022 |
| 5982 | CytomX Therapeutics South San Francisco, CA TEMP Research Associate, Protein Purification, Protein Sciences MS in Biochemistry Exp: 1 year |
We seek a highly motivated individual to support the protein production, purification and analytical method development needs for all the discovery programs at CytomX. The successful candidate will work as a TEMP Research Associate in the Protein Sciences Department up to 12 months and contribute to the lead selection process for all discovery pipeline programs including Probodies, Bispecifics and cytokines. | 10/6/2022 |
| 5983 | Debut Biotechnology San Diego, CA Research Associate: Protein Expression and Purification Master’s degree in Biology, Chemistry, Biochemistry, or other related disciplines Exp: 1+ years |
Debut Biotechnology is hiring a full-time research associate in protein expression and purification focused on cell-free biotherapeutic production. The successful candidate will work in a fast-paced team to create and test new enzymes for biotherapeutic creation and modification. Candidates must demonstrate a sense of urgency, contagious optimism, and a can-do attitude. They must lead by example and hold themselves and others accountable while maintaining productive and professional relationships within the team. We are looking for candidates with a sense of urgency, contagious optimism, and a can-do attitude. They must lead by example and hold themselves and others accountable while maintaining productive and professional relationships within the team. | 10/6/2022 |
| 5984 | Decipher Biosciences San Diego, CA Clinical Lab Technician Bachelor’s degree required Exp: 1 years’ |
The Clinical Lab Technician’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. | 10/6/2022 |
| 5985 | Decipher Biosciences San Diego, CA Research Associate I, Assay Development B.Sci. in biological sciences (or related field) Exp: 1-2 years |
The Research Associate I will support the Assay Development team at Decipher Biosciences; assisting in research, development, and optimization of genomic assays, and supporting general laboratory maintenance and document control. Other responsibilities might be applied as needed. | 10/6/2022 |
| 5986 | Deepcell Menlo Park, CA Research Associate/Senior Research Associate, System Integration Bachelor’s or Master’s degree in Bioengineering, Biomedical Engineering, or similar subject is required Exp: one year |
Come join Deepcell and make a difference! We're a small team of passionate innovators in biomedical engineering, artificial intelligence, molecular biology, and genomics. Our technology has won multiple prestigious awards and is backed by top-tier venture capitalists in Silicon Valley. | 10/6/2022 |
| 5987 | DiabetOmics Hillsboro, OR Research Assistant/Associate in Product Development (2 positions available immediately) BA/BS in a relevant biological science Exp: 1-2 years |
Diabetomics, Inc., is a leading medical diagnostics company serving the needs of personalized health and diabetes risk assessment and management. Diabetomics R&D group is currently seeking a Research Assistant/Associate to join our established team. Essential Functions: Supports the Diagnostic Product Development team. This is a hands-on, bench-level laboratory position. Tasks will include, but are not limited to: assay feasibility, assay development, optimization, reagent formulation, verification and validation studies. | 10/7/2022 |
| 5988 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 10/7/2022 |
| 5989 | Eclipse Bioinnovations San Diego, CA Bioinformatics Associate B.S. or M.S. in Bioinformatics, Computational Biology, Computer Science, Biology, or related discipline Exp: entry level |
This is an entry level position with opportunity for growth for candidates who are looking to work in the RNA field and develop their bioinformatics skills. Candidates should be highly motivated, eager to learn, and capable of communicating effectively. The primary role of a bioinformatics associate is to assist project leads with both customer and R&D analyses. | 10/7/2022 |
| 5990 | Ensoma Boston, MA Analytical Development Associate Scientist BS or MS Degree in Biology, Cell Biology, Molecular Biology or Biochemistry. Exp: 1+ years |
We are seeking a highly motivated Analytical Development Associate Scientist to join our CMC team. In this Associate Scientist role, your main responsibilities will include supporting analytical assay development and sample evaluation to enable vector production and process development teams to make informed decisions to drive drug substance and drug product development. This position will support the CMC team by performing cell culture and wet lab experiments, analyzing data, drafting protocols, procedures, and reports. A successful candidate will be responsible for planning experiments, executing protocols and will be able to summarize results independently. Should the need arise, troubleshooting experimental protocols and in collaboration with his/her supervisor and effectively implementing changes to the protocol. In this position, collaborations both within analytical development and in cross-functional groups are key to advancing novel gene therapies into the clinic.A successful candidate will be responsible for planning experiments, executing protocols and will be able to summarize results independently. Should the need arise, troubleshooting experimental protocols and in collaboration with his/her supervisor and effectively implementing changes to the protocol. In this position, collaborations both within analytical development and in cross-functional groups are key to advancing novel gene therapies into the clinic.We are seeking a highly motivated Analytical Development Associate Scientist to join our CMC team. In this Associate Scientist role, your main responsibilities will include supporting analytical assay development and sample evaluation to enable vector production and process development teams to make informed decisions to drive drug substance and drug product development. This position will support the CMC team by performing cell culture and wet lab experiments, analyzing data, drafting protocols, procedures, and reports. | 10/7/2022 |
| 5991 | Etubics Culver City, CA Research Associate B.S. in biochemistry or in related scientific disciplines Exp: 1-2 years |
ImmunityBio Inc. is seeking a highly motivated, full-time research associate to join the Protein Science group to support the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate should have a bachelor’s degree with 1-2 years of wet-lab experiences, ability to manage multiple tasks in a timely manner, good written/verbal communication skills and have a willingness to work as part of the team. | 10/7/2022 |
| 5992 | Etubics Culver City, CA Research Associate II B.S. in biochemistry or in related scientific disciplines Exp: 1-3 years |
ImmunityBio Inc. is seeking a highly motivated, full-time research associate to join the Protein Science group to support the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate should have a bachelor’s degree with 1-3 years of wet-lab experiences or a master’s degree with 1+ year of wet-lab experience, ability to manage multiple tasks in a timely manner, good written/verbal communication skills and have a willingness to work as part of the team. | 10/7/2022 |
| 5993 | Evelo Biosciences Cambridge, MA Formulation Research Associate B.S. or M.S in Pharmaceutical Sciences, or Chemical Engineering preferred Exp: 1-5 years’ |
Evelo Biosciences is seeking a Formulation Research Associate to support our dynamic and growing organization. Evelo Biosciences, Inc. (Nasdaq: EVLO) a biotechnology company developing a new modality of orally delivered, systemically acting biologics that could disrupt the industry is looking for a highly motivated individual who is energized by the prospect of working in a clinical stage company, has a strong desire to learn, and wishes to be an integral member of an interdisciplinary team. This critical role will be responsible for providing essential scientific support to the Formulation Team in a fast-paced, dynamic and intellectually challenging environment. The successful candidate should have basic knowledge of chemistry and be proficient in standard laboratory operations such as weighing, mixing, characterizing powders, conducting experiments, performing data analysis, draft reports, present results, and possess the ability to multi-task within scope in a timely manner. | 10/7/2022 |
| 5994 | Flexion Therapeutics San Diego, CA QA Associate 2 - Raw Materials BS/BA degree in scientific discipline from an accredited college or university or equivalent experience. Exp: 1-3 years |
This person is to assist and support the organization with GMP compliance; monitoring of conformance to established quality assurance processes and GMP standards in release of raw materials. | 10/7/2022 |
| 5995 | Fluxenergy Irvine , CA Research Associate - Microfluidics, Irvine Bachelor of Science degree or Master's degree in Life Science or Engineering disciplines or related fields Exp: 0-2 years |
As a Research Assistant at Fluxergy, you will be directly iinvolved in the company's Card R&D activities, as well as deeply involved with the company's long-term strategy. You will be repsonsible for helping develop the next generation of Fluxergy Test Card, a microfluidic consumable aiming at transforming point-of-care diagnostic systems. You will be expected to conduct, analyze, and report on experiments to develop new Test Card from feasibility through validation for the Fluxergy platform. You will work closely with a cross discipline team of R&D and Production Engineers and Technicians to develop new products. This position requires a highly motivated, independent worker who has a strong desire to bring products to the market. | 10/7/2022 |
| 5996 | Fluxenergy Irvine , CA Industrial Engineer, Irvine Bachelor’s degree or Masters' degree in Industrial Engineering Exp: 1-3 years |
As the Industrial Engineer at Fluxergy, you will be directly involved in the company’s Production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process improvement, scale up and capacity planning while working with a small but passionate team. This position requires a deep, in-depth knowledge of lean manufacturing and six sigma methodologies. | 10/7/2022 |
| 5997 | Fluxenergy Irvine , CA Process Engineer, Irvine Bachelor's Degree or Master's Degree in an engineering field Exp: 0-2 Years |
As the process engineer at Fluxergy, you will be directly involved in the company’s production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process ownership while working with a small but passionate team. This position requires a deep, in-depth knowledge of manufacturing processes, stability and process control. | 10/7/2022 |
| 5998 | Foghorn Therapeutics Cambridge, MA NEW Research Associate - Biochemistry Biophysics BA/BS or MS degree in Biochemistry or Biophysics, or life sciences or biotechnology Exp: 1-3yrs+ years |
Foghorn is seeking a highly motivated, enthusiastic, and collaborative Research Associate to join our Drug Discovery team in a lab-based role to support early discovery projects in oncology. As a member of our Drug Discovery team the candidate will have an opportunity to employ various biochemical and biophysical assay technologies in mechanism of action studies, screening, and hit validation. Training is provided. This job is onsite and located in Cambridge, MA. | 10/7/2022 |
| 5999 | Foghorn Therapeutics Cambridge, MA Senior Research Associate - Translational Biomarkers Master of Science Exp: 1 year or more |
Conduct exploratory research to help identify new tumor- and peripheral-based biomarker assays for emerging clinical programs utilizing in vitro/ex vivo/in vivo model system Work with Biology and Pharmacology groups to acquire, process, and analyze samples to generate internal datasets necessary for assay development and pre-clinical proof of concept for clinical biomarkers (e.g. qPCR, FACS, ELISAs, etc.) Test new technologies in house and develop exploratory assay systems to answer key questions relevant to Translational Biomarker Plans for Clinical Programs | 10/7/2022 |
| 6000 | Capricor Therapeutics Los Angeles, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences or related field Exp: 1-3 years |
This position is immediately available to join our Manufacturing team to perform cGMP manufacturing to support Capricor’s clinical trials and exosome development. Capricor is developing its exosome technology as a next-generation therapeutic platform. The Company’s current focus is on developing exosomes capable of delivering nucleic acids, including mRNA as well as proteins, to treat or prevent a variety of diseases. We are seeking an individual with a scientific background, mammalian cell culture and cGMP experience. | 9/27/2022 |
| 6001 | Capricor Therapeutics San Diego, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences or related field Exp: 1-3 years |
This position is immediately available to join our Manufacturing team to perform cGMP manufacturing to support Capricor’s clinical trials and exosome development. Capricor is developing its exosome technology as a next-generation therapeutic platform. The Company’s current focus is on developing exosomes capable of delivering nucleic acids, including mRNA as well as proteins, to treat or prevent a variety of diseases. We are seeking an individual with a scientific background, mammalian cell culture and cGMP experience. | 9/27/2022 |
| 6002 | CareDx Brisbane, CA Clinical Lab Assistant | Job # 1111 BS/BA in a biology-related science is preferred Exp: 1-3 years |
Clinical Laboratory Assistant (Tuesday-Saturday) The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed | 9/27/2022 |
| 6003 | CareDx Brisbane, CA Clinical Lab Assistant | Job # 1455 BS/BA in a biology-related science is preferred Exp: 1-3 years |
Clinical Laboratory Assistant (Tuesday-Saturday, 2PM - 10:30PM) The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed. | 9/27/2022 |
| 6004 | Abcam Fremont, CA Research Associate/Sr. Research Associate BS Degree in biochemistry, pathology, cell and molecular biology, immunology or other Life Sciences. Exp: 0-3 years |
Focus on the development and validation of qualified antibodies for IVD immunohistochemistry (IHC) applications under FDA and MDSAP/ISO13485 (2016) quality standards. | 9/27/2022 |
| 6005 | Abcam Eugene, OR Research Associate B.S. in Biology, or closely related discipline Exp: 1 year |
We are seeking a Research Associate to assist in the development of novel immunoassays in our Eugene, OR facility. The core responsibility will be to provide support to the SimpleStep immunoassay development team through the use of antibody-based laboratory techniques such as sandwich ELISA, Western blot, immunocytochemistry, and flow cytometry as well as the generation of biological materials for analysis. | 9/27/2022 |
| 6006 | Bachem Torrance, CA Production Chemist BS degree in Chemistry or related field Exp: 1-5 years’ |
The Chemist function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. | 9/28/2022 |
| 6007 | Bachem Vista, CA Production Chemist BS degree in Chemistry or related field Exp: 1-5 years’ |
The Chemist function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. | 9/28/2022 |
| 6008 | BioMarin Pharmaceutical Novato, CA Research Associate I Bachelor’s Degree in Chemistry, Biochemistry, Analytical Chemistry, or a related field Exp: 0 - 2+ years |
The selected candidate will work in the Analytical Sciences group to assist in the advancement of BioMarin’s therapeutics for clinical evaluation and potential commercialization. The candidate will be responsible assay development, assay qualification, and characterization testing using routine and semi-routine analytical methods under limited supervision. The selected candidate should possess excellent analytical, organizational and communication skills and be a self-starter willing to work efficiently and collaboratively in a dynamic environment. | 9/28/2022 |
| 6009 | Bristol-Myers Squibb Devens, MA QC Microbiology Associate BS/BA in biological sciences, or its equivalent in experience. Exp: 0 to 2 years |
This position is Wednesday through Saturday 1st shift position. 7am-5pm | 9/28/2022 |
| 6010 | Bristol-Myers Squibb Seattle, WA Research Associate- Cell Core B.S. in Biology, Chemical Engineering, Bioengineering or relevant scientific discipline Exp: 0-2 years |
Cell Core is responsible for supplying cellular products to support internal development organizations. This role will be responsible for fielding requests for cellular products and managing communications related to coordination and fulfillment of requests in support of Quality and Analytical Development functions. These communications will occur within and between varied company levels and internal organizations. The role will therefore require a high degree of approachability and interpersonal savvy, with a proven ability to work in cross-functional teams. Effective organizational skills will also be necessary as the candidate will be responsible for operating within the request fulfillment schedule, documenting operating activities, and organizing large quantities of data. Experience culturing mammalian cells is strongly preferred. | 9/28/2022 |
| 6011 | Bristol-Myers Squibb New Brunswick, NJ BACTERIOLOGIST Bachelors' degree with a major in biology, or an allied science and coursework in microbiology from an accredited college or university. Exp: 1 year |
Performs microbiological testing to ensure that the proper standards of quality are maintained. Performs microbiological, bacterial endotoxin, total organic carbon and conductivity analyses of water system samples. Performs environmental monitoring and water sampling in support of the routine operations and manufacturing. Demonstrates the use of aseptic technique. Analyzes, develops and recommends new methods for the improvement of various standard assays and tests. Carries out analytical tests and inspections in connection with the investigation of product and environmental monitoring excursions. Evaluates results and submits documentation for approval. Performs routine maintenance and calibration procedures on laboratory instrumentation. Troubleshoots equipment and methods for investigational purposes. Performs laboratory support activities such as stock culture maintenance and laboratory inspections, as assigned. Responsibilities include maintaining laboratory documentation, samples, and equipment under strict compliance with safety, GMP, federal, state and local regulations. Maintains laboratory notebook (paper or electronic), record/capture records raw data, calculates results and submit results to laboratory supervisor and/or computer database following Good Documentation Practices. | 9/28/2022 |
| 6012 | Bristol-Myers Squibb Phoenix, AZ Analyst I Bachelor’s Degree, particularly in Microbiology or Science related field, preferred. Exp: 1 year |
The Analyst I, QC Microbiology, is responsible for routine and non-routine microbiological testing and environmental monitoring in support of sterile product manufacturing. The Analyst I is also responsible for peer review, training, supporting document management, projects, CAPAs and investigations in accordance with the organization’s policies, procedures, and state, federal and local laws and ensure compliance with current Good Manufacturing Practices (cGMP), USP, EP, JP and other regulatory requirements at all times. | 9/29/2022 |
| 6013 | Bristol-Myers Squibb Seattle, WA Associate/Senior Associate Scientist, Analytical Operations- Cell Therapy Associate scientist requires BS in a scientific discipline; Sr Associate scientist requires MS in a scientific discipline. Exp: BS: 1+ year ; MS: 1+ years |
Cell Therapy Product and Analytical Development (P&AD) is seeking an enthusiastic, self-driven Associate/Senior Associate Scientist to join its Analytical Operation team that values data quality, high productivity and team‐work . In this individual contributor, lab-based role, the Associate/Senior Associate Scientist will work in a collaborative environment to perform various analytics testing for process development and product characterization to support BMS cell therapy programs. This position will report to the supervisor of Analytical Operation. The successful candidate must have hands on experience with various bioanalytical techniques including ELISA, qPCR, ddPCR and flow cytometry and the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. | 9/29/2022 |
| 6014 | Bristol-Myers Squibb Summit, NJ Assistant / Associate / Sr. Associate Scientist, Biologics Manufacturing – Downstream Operations Biology, Biochemistry, Bioengineering, Biochemical, Chemical Engineering or related discipline. Assistant Scientist - BA/BS ; Associate Scientist – MA Exp: BA/BS: 0-2 yrs; MA/MS: 0-2 years |
We are currently looking for an Assistant Scientist, Associate Scientist OR Senior Associate Scientist to join our Biologics Manufacturing Team within the BMS’s Biologics Development & Manufacturing group in Summit, New Jersey. As a member of the Biologics Development & Manufacturing group, the Assistant / Associate / Sr. Associate Scientist will provide technical and operational expertise and oversight to early stage clinical manufacturing campaigns. The focus of this position will be on downstream operations and support of upstream operations in single-use manufacturing environment. | 9/29/2022 |
| 6015 | Covance Somerset, NJ Study Technician - Animal Operations Bachelor Degree Exp: No experience is required |
In this animal-based role, you’ll collect, document and manage data that includes animal observations, test material administration and clinical samples. This is a hands on, physically demanding role working directly with animals daily. | 9/29/2022 |
| 6016 | Covance Madison; Somerset; Greenfield, WI Study Technician- Animal Operations (3 locations) Bachelor degree in Life Sciences Exp: current student |
**Applicants for this role must be a current student with intentions to graduate between December 2022 and May 2023** In this animal-based role, you’ll collect, document and manage data that includes animal observations, test material administration and clinical samples. This is a hands on, physically demanding role working directly with animals daily. | 9/29/2022 |
| 6017 | Covance Madison; Somerset; Greenfield, WI Study Technician- Anatomical Pathology (3 locations) Bachelor’s Degree in Life Sciences, or Associate Degree in Life Sciences, Histology, Laboratory Animal Technology or Veterinary Technology; experience Exp: current student |
**Applicants for this role must be a current student with intentions to graduate between December 2022 and May 2023** In this animal-based role, you’ll collect, document and manage data that includes animal observations, test material administration and clinical samples. This is a hands on, physically demanding role working directly with animals daily. | 9/29/2022 |
| 6018 | Covance Raritan, NJ Medical Technologist/Clinical Laboratory Scientist - Molecular Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Tuesday - Saturday (3:00pm – 11:30pm) | 9/29/2022 |
| 6019 | Covance Raritan, NJ Medical Technologist/Clinical Laboratory Technician – Immunology Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be: Tuesday - Saturday 2.00 pm to 10.30 pm – Rotating Sundays | 9/29/2022 |
| 6020 | Covance Raritan, NJ Medical Technologist/Clinical Laboratory Technician – Hematology Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Monday-Friday 11:00 PM- 7:30 AM & alternating SaturdayAre you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Monday-Friday 11:00 PM- 7:30 AM & alternating Saturday | 9/29/2022 |
| 6021 | Exact Sciences Phoenix, AZ Molecular Technologist I Molecular Technologist I Bachelor's Degree in Biology, Chemistry, Biochemistry, Life Sciences, or field as outlined in the essential duties. Exp: 1+ years |
The Molecular Technologist I will isolate and quantify nucleic acids, perform polymerase chain reaction (PCR) tests and next generation sequencing (NGS), library construction, and other NGS-associated procedures. | 9/29/2022 |
| 6022 | Exact Sciences Madison, WI Laboratory Service Engineer I - Tuesday-Friday, 2:00pm-1:00am Bachelor’s degree in Engineering, Technology, Molecular Biology, Electronics, or related field Exp: 1+ years |
The Laboratory Service Engineer I (LSE I) is responsible for the Instrument and Automation Services of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Engineers (LSE) and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. The LSE I may work continuously with other LSEs and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. | 9/29/2022 |
| 6023 | Exact Sciences Cambridge, MA Laboratory Service Engineer I - $10,000 Sign-on Bonus! Bachelor’s degree in Engineering, Technology, Molecular Biology, Electronics, or related field Exp: 1+ years |
The Laboratory Service Engineer I (LSE I) is responsible for the Instrument and Automation Services of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Engineers (LSE) and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. The LSE I may work continuously with other LSEs and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. We are offering a $10,000 sign-on bonus to external candidates. | 9/29/2022 |
| 6024 | Exact Sciences Redwood City, CA Laboratory Service Engineer I Laboratory Service Engineer I Bachelor’s degree in Engineering, Technology, Molecular Biology, Electronics, or related field Exp: 1+ years |
The Laboratory Service Engineer I (LSE I) is responsible for the service and support of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Engineers (LSE) and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. The LSE I may work continuously with other LSEs and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. | 9/30/2022 |
| 6025 | Eli Lily Cambridge, MA Biologist-Obesity Research Master’s degree in biology or a closely related field Exp: research experience |
The Diabetes, Obesity and Complications Therapeutic Area (DOCTA) of Eli Lilly and Company, is focused on the discovery of biologic, small molecule and genetic therapeutics for the treatment of diabetes, obesity and associated complications. We are seeking an individual with training in molecular biology, cell culture and biochemistry, as well as broad experience in metabolic disease programs, who can succeed in a highly collaborative team environment. The successful candidate will play a meaningful role in supporting discovery efforts and established pipeline projects with an emphasis on anti-obesity therapeutics. You will be responsible for setting up critical capabilities in the laboratory setting and working with other scientists within and across departments to achieve project goals. We are a growing group passionate about our research and how it impacts Lilly's mission of improving lives. | 9/30/2022 |
| 6026 | Eli Lily Indianapolis, IN Chemist - SMDD MS degree in synthetic organic chemistry or related field Exp: |
Lilly’s Synthetic Molecule Design and Development (SMDD) organization engages in design and development activities for small molecules, peptides and oligonucleotides from pre-clinical phases through commercialization for drug substances and drug products. Our scientists develop solutions using their deep technical expertise to enable testing of clinical hypotheses and accelerate drug development. SMDD excels in these areas by placing innovation at the heart of what we do. Our innovation engine is driven by an array of diverse talents and cultures brought together in state of the art laboratory and open concept facilities which foster collaboration and teamwork. Our team is looking for creative candidates to contribute to our synthetic molecule route design and development portfolio | 9/30/2022 |
| 6027 | AI Therapeutics Madison, WI Associate Analytical Chemist 1st Shift - $3,000 Sign On Bonus Bachelor’s Degree in relevant field (laboratory experience may be substituted for a degree) Exp: Entry-Level |
We test of a variety of instrumentation including UPLC, HPLC, GC, and LCMS technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of analytical instruments! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you! | 9/30/2022 |
| 6028 | AI Therapeutics Cambridge, MA Research Associate (Separations + Biophysical) Bachelor’s Degree/ Master's Degree in related science Exp: BS: 0-2+ years; 0+ years |
Provide timely internal non-GMP testing support for various teams Support automation of analytical workflows and qualification of automated assays Document lab work and results in ELN and/or LIMS Coordinate, store, and properly handle samples and retains Manage and track supply of controls, reference standards, and critical reagents Train other analysts as necessary Ensure Instruments and lab are properly maintained Work with many other groups to support client's mission | 9/30/2022 |
| 6029 | AI Therapeutics Cambridge, MA Research Associate Degree in Cell and Molecular Biology, Biochemistry, Pharmaceutical, or other biological/analytical discipline Exp: BS: 0-2+ years; 0+ years |
Supports viral vector process development by providing analytical testing on DNA, ELISA, cell based platform within agreed upon turn-around Demonstrate good understanding of ongoing programs and data generated in relation to the program Troubleshoots issues as needed with supervision Monitors assay performance to ensure GLP compliance Maintains equipment and critical reagent inventory Provides testing support to aid viral vector development to support cell therapies in a fast paced and dynamic team environment. | 9/30/2022 |
| 6030 | AI Therapeutics Foster City, CA HPLC Research Associate Bachelor's/Master's Degree Exp: BS: 0 - 3 years; MS: 1+ year |
Plans and executes assigned experiments that support non-routine development activities and project goals Conduct analytical methods including UPLC/HPLC, Dissolution, GC, Thermogravimetric DSC/TGA, and KF titration Perform data analysis and troubleshoot methods and instrumentation Recommends alternatives, researches new methods and techniques and may proactively seek out senior personnel to discuss potential solutions to problems. Prepare data for presentation and assist in generating technical reports, and interact with other groups within the department Perform review and peer review of analytical data Initiate and perform investigations and development, as needed Ensure project deliverables are scientifically accurate and meet timeline expectations | 9/30/2022 |
| 6031 | AI Therapeutics Cambridge, MA Research Chemist (HPLC and CE) Bachelor’s Degree in related science; Master’s Degree in related science Exp: BS: 1-2+ years; MS: 0+ years |
Provide timely internal non-GMP testing support for various teams Support automation of analytical workflows and qualification of automated assays Document lab work and results in ELN and/or LIMS Coordinate, store, and properly handle samples and retains Manage and track supply of controls, reference standards, and critical reagents Train other analysts as necessary Ensure Instruments and lab are properly maintained Work with many other groups to support client's mission | 9/30/2022 |
| 6032 | AI Therapeutics San Diego, CA Research Associate I in vivo Bachelor’s degree in life sciences or related discipline required. Exp: 0-2 years |
The successful candidate for the Research Associate I position will join the Beacon Discovery team with a multifaceted approach for providing high value services based on the Beacon Discovery platform and other proprietary technologies. The position provides an outstanding opportunity to learn new techniques and develop skills within a dynamic in vivo pharmacology research team. We work with multiple animal models, from anxiety to metabolism and beyond. If you are interested in working in a fast paced, challenging environment where you will have an opportunity to learn and succeed this may be the place for you. Laboratory experience with animal handling and pharmacology studies would be advantageous but is not necessary. Extensive training will be provided. | 9/30/2022 |
| 6033 | Cellular Dynamics Madison, WI Facility Management Specialist/Facilities Engineer - (#398) Bachelor’s degree in engineering or construction related field, or equivalent experience Exp: One year |
We are recruiting for a Facility Management Specialist (AKA Facilities Engineer) to support our investment in and on-going operation of our cGMP, research and development, and production facilities in Madison, WI. You'll be part of the technical operations group along with other highly talented professionals at FUJIFILM Cellular Dynamics, Inc., the leader in induced Pluripotent Stem Cells (iPSC’s) technology. In this role you'll oversee all aspects of facility operation and maintenance including commissioning, qualification, maintenance, and calibration of facility, equipment, systems and utilities for all FCDI facilities. This is an excellent opportunity for qualified individuals looking to apply their technical skills and to expand their professional horizons. | 9/30/2022 |
| 6034 | Cellular Dynamics Madison, WI cGMP Biomanufacturing Specialist - (#341) Bachelor’s degree in cell biology, molecular biology, biochemistry or related technical field Exp: BS Degree |
FUJIFILM Cellular Dynamics, Inc in Madison, WI is recruiting for a cGMP bio-manufacturing specialist This role provide outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate differentiated cell types from human induced pluripotent stem cells. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. In return we provide development and support to enhance your career using cutting edge iPSC technology. | 9/30/2022 |
| 6035 | Cellular Dynamics Madison, WI Undergraduate Research Assistant - (#376) High school diploma, with relevant coursework progressing to a bachelor’s degree in biologic sciences, or related field Exp: Undergraduate |
FUJIFILM Cellular Dynamics, Inc is recruiting for undergraduate research assistants to work in our research and development, and bioinformatics facility in Madison, WI. This role provides an outstanding opportunity for a dedicated and responsible individual to learn, develop, and contribute to maintaining and improving lab operations, along with supporting research and development projects. And, as required, participate in cellular and molecular projects. Ideal candidates will demonstrate a track record of self-motivation, strong organizational skills, and dedication to their work. The role requires at least 10 hours per week of commitment with flexible scheduling, and with the ability to also work on weekends as required. | 9/30/2022 |
| 6036 | Steris Plymouth, MN Software Engineer Bachelor's Degree. Exp: 0-3 years |
The Software Engineer is responsible for the design, development and deployment of complex SQL database software intended for use as standalone databases or for use in MEDIVATORS, Cantel Medical, and STERIS medical devices. | 9/30/2022 |
| 6037 | Steris Sharon, PA Quality Engineer Bachelor's Degree in Engineering General Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 9/30/2022 |
| 6038 | Steris Rush, NY Quality Engineer Bachelor's Degree Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 9/30/2022 |
| 6039 | Steris Mentor, OH Cybersecurity Software Development Engineer Bachelor in Computer Engineering, Computer Science, Software Engineering, Electrical Engineering, or Cybersecurity required. (A degree in another En Exp: 1+ years |
Join an organization and a team where you can have an impact on creating a healthier and safer world. As a Software Engineer within the Infection Prevention Technology (IPT) Team you will work within a software development team to achieve and maintain the security of medical equipment connected to local hospital networks and remote applications in the cloud. You will be an active participant in the corporate cybersecurity working group to share best practices, software tools, vendor selection, and other cybersecurity related activities. The Software Engineer will also support multiple product development and product sustaining teams in security related product requirements, design specifications, risk analysis, and verification, as well as develop work instructions for the maintenance and verification of security for product software. *This role allows for hybrid work options | 9/30/2022 |
| 6040 | Ascendis Pharma Redwood City, CA Research Associate, Development Chemistry Masters Degree in organic, polymer or bio-chemistry or related field. Exp: 0-3 yrs |
The successful candidate will be responsible for conducting laboratory-based process chemistry activities to support Ascendis Pharma’s growing pipeline of pre-clinical and clinical programs. Working closely with a team of scientists and engineers in Ascendis Pharma’s Redwood City laboratory, the successful candidate will be responsible for process chemistry research and development such as process optimization and scale-up. This position offers great potential for scientific growth and gain of CMC knowledge while working on developing exciting, complex, and impactful drugs for patients. | 9/18/2022 |
| 6041 | Ascendis Pharma Redwood City, CA Research Associate, Process Development Bachelor’s degree in chemistry, biochemistry, biotechnology, or a related field or MS graduate - new grads are welcome to apply! Exp: New Grads |
In this position you will be responsible for conducting laboratory experiments related to the development, characterization, scale up of a manufacturing process for our localized delivery technology platform. Working closely with a team of scientists/engineers in our new Redwood Shores facility, the Associate Scientist will characterize and investigate novel and existing processing steps used to manufacture products in our growing portfolio. This position offers great potential for growth of scientific and drug development experience while working on exciting, complex, and impactful products | 9/18/2022 |
| 6042 | Ascendis Pharma Redwood City, CA Research Associate Bachelor’s degree in chemistry, biochemistry, biotechnology, or a related field or MS graduate - new grads are welcome to apply! Exp: New Grads |
In this position you will be responsible for conducting laboratory experiments related to the development, characterization, scale up of a manufacturing process for our localized delivery technology platform. Working closely with a team of scientists/engineers in our new Redwood Shores facility, the Associate Scientist will characterize and investigate novel and existing processing steps used to manufacture products in our growing portfolio. This position offers great potential for growth of scientific and drug development experience while working on exciting, complex, and impactful products | 9/18/2022 |
| 6043 | Astellas South San Francisco, CA Research Associate II, Cell Biology in South San Francisco, California MS Degree Exp: 0-2 years |
The primary purpose of the Research Associate II is to support all lentiviral production and immune cell manufacturing needs as well as cell biology and assay development in support of research activities. This position will work primarily in a laboratory setting with Scientist and research and discovery teams. | 9/18/2022 |
| 6044 | Astellas Westborough, MA Research Associate II, Stem Cell Research in Westborough, Massachusetts MS Degree Exp: 0-2 years' |
Performs experiments and progress research and/or development in collaboration with others. Makes detailed observations, analyzes data and interprets results. Investigates, creates and develops new methods and technologies for project advancement. | 9/18/2022 |
| 6045 | Astellas Westborough, MA Research Associate II, Cell Based Therapies in Westborough, Massachusetts MS Degree Exp: 0-2 years |
We are seeking a highly motivated and energetic Research Associate to join the Research and Development team. This candidate will assist and troubleshoot exploratory research projects by performing mammalian cell culture, cell, and molecular biology, and maintain accurate records for potential clinical applications. This position is highly collaborative, with on-the-job training to support the driven candidate's development and success. | 9/18/2022 |
| 6046 | Astellas Seattle, WA Research Associate II, Clinical Gene Editing in Seattle, Washington MS Degree Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 9/19/2022 |
| 6047 | Astellas Seattle, WA Research Associate II, Process Development in Seattle, Washington MS Degree Exp: 0-2 years |
The primary purpose of the Research Associate II for Process Development is to execute experiments to improve clinical-grade, gene-editing processes of Universal Donor Cells and to provide data for CMC documents. This Research Associate II role will work as part of a team evaluating processes, and planning/executing experiments to evaluate all aspects of culturing, gene-editing, and processing of pluripotent stem cells. This position will be provided training to perform all required fundamental skills. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 9/19/2022 |
| 6048 | Astellas Seattle, WA Research Associate II, Cell Analytics in Seattle, Washington MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the molecular engineering and characterization for our gene edited Universal Donor Cells, by utilizing various cell culture techniques. They will work as a key member on a fast paced team to culture pluripotent stem cells as well as run cellular assays to characterize our proprietary Universal Donor Cells. | 9/19/2022 |
| 6049 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters Exp: 0-1 years |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 9/19/2022 |
| 6050 | Avedro San Clemente, CA MANUFACTURING TECHNICIAN III, PHARMACEUTICAL bachelor’s degree in science or engineering. Exp: 0+ years’ |
Follow, execute, and adhere to documentation in accordance with cGMP, QSR, and GDP requirements: protocols, specifications, work instructions (WIs), standard operating procedures (SOPs), BRs, and DHRs. | 9/19/2022 |
| 6051 | Avitide Lebanon, NH Manufacturing Technician Bachelor degree in Biotechnology or Biology (or related field) Exp: 1-2 years’ |
This qualified candidate will join the growing manufacturing team responsible to produce Avitide AVIPure® biopharmaceutical affinity chromatography products. The individual will be involved in all aspects of product manufacturing including buffer preparation, reactor set-up, production, product packaging and cleaning. Work will be performed in accordance with established manufacturing practices and procedures in compliance with our ISO 9001 quality regulations and guidelines. Avitide seeks candidates who are highly self-motivated and can work in a collaborative fashion with other interdisciplinary team members in a fast-paced and exciting work environment. | 9/20/2022 |
| 6052 | Axial Therapeutics Woburn, MA Research Associate/Senior Research Associate - Biosciences Bachelor’s degree in biology, biochemistry, or a related field preferred. Exp: 1-3 years |
In this role the Research Associate will support biology as a member of a highly matrixed drug discovery team and will be responsible for the execution and troubleshooting of various cell-based and biochemical assays and experiments. The Research Associate will contribute to drug screening and mechanism-of-action studies for projects in immuno-oncology and neurological diseases and disorders and have opportunities to contribute to new target discovery and validation. This proactive researcher will collaborate with team members, identify opportunities to improve efficiency, share ideas and expertise and contribute to Axial’s creative, dynamic, and collaborative culture. | 9/20/2022 |
| 6053 | Azzur Totowa, NJ Chemist of Research and Development (1-3 years experience) M.Sc. or BS in Chemistry or Chemical Engineering is required. Exp: 1-2 + years |
• Develop new chemical methods for analysis and equipment for implementation purposes. • Develop analytical methods for process solutions used in metal deposition and other areas of semiconductor manufacturing. • Interface with engineering group to design commercial analyzers. • Plan and conduct experiments then write technical report findings. • Participate in documenting, testing and supporting equipment. • Validate analytical methods developed in R&D department, update documentation and prepare reports. • Prepare scientific publications and present work at conferences. | 9/20/2022 |
| 6054 | Berkshire Sterile Manufacturing Lee, MA Process Engineering Associate Process Engineer: Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science Exp: (1) year |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 9/20/2022 |
| 6055 | Biocare Medical Pacheco, CA Associate I, Protein Chemistry Bachelor’s degree in a scientific field Exp: one plus (1+) years’ |
The Protein Chemistry Associate I will take an active role in material processing, reagent formulation, technical manufacturing, and in-process and/or final quality control of reagents for use as components of in-vitro diagnostic (IVD) products. Specifically, he/she is involved in bioconjugation, protein purification, and analytical characterization of complex bioconjugates as they relate to the development of tissue diagnostic products for cancer and infectious disease. This position requires the person to adhere to all current industry standard regulations. | 9/20/2022 |
| 6056 | Biocoat Horsham, PA Coating Development Engineer Bachelor of Science in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, or other related engineering field. Exp: 1 year |
Biocoat is a global leader in developing, manufacturing, and applying hydrophilic coatings to medical devices. The team needs an Engineer who would be responsible for developing coating processes and formulations for customer’s devices as well as optimize coating parameters. | 9/20/2022 |
| 6057 | Biocoat Horsham, PA Research and Development Technician B.S. in Chemistry, Biochemistry, or similar focus. Exp: 1-3 years |
Biocoat is the global leader in developing, manufacturing, and applying coatings on medical devices. We are looking for a dynamic and dedicated full-time Research and Development Technician! | 9/20/2022 |
| 6058 | Biomere Richmond, CA Research Associate (Small & Large Animal) BS Degree in Science (or equivalent degree) preferred. Exp: Research Associate I: 1 or 2 years |
Research Associate works under the direct guidance of the Site Head and the general guidance of the senior staff. Research Associate is proficient in animal procedures/animal husbandry, grant, internal, and/or contract research studies according to the study protocols and to the company guidelines and standard operating procedures (SOPs). | 9/20/2022 |
| 6059 | PSC Biotech Durham, NC Junior CSV Engineer Degree or Certification in Engineering Exp: 1-3 years |
We are hiring junior-level CSV Engineers to support Rockwell Automation and Process Control systems. The CSV Engineer is responsible for performing Computer Systems Validation of a PLC Rockwell for a GMP manufacturing process including qualification protocol development (IOQ) and execution. | 9/21/2022 |
| 6060 | PSC Biotech Philadelphia, PA Junior CSV Engineer Degree or Certification in Engineering Exp: 1-3 years |
We are hiring junior-level CSV Engineers to support Rockwell Automation and Process Control systems. The CSV Engineer is responsible for performing Computer Systems Validation of a PLC Rockwell for a GMP manufacturing process including qualification protocol development (IOQ) and execution. | 9/21/2022 |
| 6061 | PSC Biotech Newark, NJ Junior CSV Engineer Degree or Certification in Engineering Exp: 1-3 years |
We are hiring junior-level CSV Engineers to support Rockwell Automation and Process Control systems. The CSV Engineer is responsible for performing Computer Systems Validation of a PLC Rockwell for a GMP manufacturing process including qualification protocol development (IOQ) and execution. | 9/21/2022 |
| 6062 | PSC Biotech Thousand Oaks, CA Mechanical/Project Engineer Bachelor Degree in Engineering Exp: 1-3 years |
We are hiring a Mechanical/Project Engineer to assist the assessment of pressure safety devices. This position is full-time and on-site in Thousand Oaks. | 9/21/2022 |
| 6063 | Blue Rock Therapeutics Toronto, ON Research Associate, Formulation Development Masters degree in Biomedical, Chemical, Material, Biological or Pharmaceutical Sciences or Engineering Exp: 0-3 years |
We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives. As part of BlueRock Therapeutics’ vision to change the future of medicine by enabling ground-breaking cell therapies, the candidate will be a key technical contributor of a dynamic and innovative team developing formulations for cellular medicines. The successful candidate will support development of cellular drug product formulations at BlueRock by identifying, designing and testing formulations to optimize cellular drug product in-use stability, cell dose delivery, and cell persistence after transplantation. The ideal candidate will be a highly motivated individual who has demonstrated strong bench skills, excellent documentation skills, attention to detail and enjoys working in a highly cross-functional environment. | 9/21/2022 |
| 6064 | Blue Rock Therapeutics New York City, NY Research Associate I-II, PSC Biology and Differentiation Bachelor’s degree or MSc. preferred field of study includes, but not limited to, biomedical sciences, stem cell biology, bioengineering, biochemistry. Exp: BS: 0-5 years; MSc.: 0-3 years |
We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives. The New York, USA site is seeking an RA I-II PSC Biology and differentiation. The ideal candidate will join a team that spearheads our technological and innovative advancement of pluripotent stem cell (PSC) biology, characterization, and production. The individual will plan and execute experiments, keep meticulous records of experimental details, analyze, and interpret datasets. The ideal candidate will enjoy a unique career development environment by interacting with several teams across R&D and manufacturing. The candidate will work closely with scientists from platform and cell biology teams and develop scientific skillsets. | 9/21/2022 |
| 6065 | Blue Rock Therapeutics New York City, NY Research Associate I/II, Genome Engineering B.Sc. or M.Sc. in cell biology, molecular biology, genetics or related discipline Exp: BS: 0-5 years; MSc.: 0-3 years |
We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives. The New York, USA site is seeking a Research Associate I or II for the Genome Engineering pipeline that will be reporting to the team lead. The incumbent will be a technical contributor in a dynamic and progressive team pioneering the generation of genome-modified therapeutic cells from human pluripotent stem cells (hPSCs). The individual will participate in the execution of a variety of genetic modifications that enhance cellular properties by employing various gene editing technologies including homologous recombination and CRISPR/Cas to establish cell lines for BlueRock’s research pipeline. The individual will also perform directed differentiation of engineered hPSC lines to determine whether these genome alterations provide BlueRock authentic cell types with novel morphology or function for the replacement of cells that have been damaged or lost to disease. | 9/21/2022 |
| 6066 | Blue Rock Therapeutics New York City, NY Research Associate I, Translational Neuroscience B.S. in Cell Biology, Molecular Biology, Neuroscience, or related discipline Exp: 0-2 years |
BlueRock Therapeutics is seeking a Research Associate I, Translational Neuroscience, based at our New York City location, reporting to the team lead and working closely with colleagues on the team. The incumbent will be a technical contributor on a team responsible for the generation and characterization of pluripotent stem cell derivatives. They will participate in efforts to maintain and characterize pluripotent stem cell (hPSC) cultures, as well as to leverage PSCs for diverse studies of directed differentiation and maturation of specified cell types. Hands-on experience in mammalian cell culture is essential. Experience with human pluripotent stem cells, directed differentiation, cell-based assays, primary cell culture, and/or neurobiology is a plus. The incumbent will work closely with several collaborating teams. This is an outstanding opportunity for a talented individual to contribute to bringing a new class of medicines to patients and gain valuable career experience in the cell therapy space. Collaboration with a highly motivated, world-class team of scientists and engineers promises an exciting and engaging work environment for motivated candidates. | 9/21/2022 |
| 6067 | Blue Rock Therapeutics Toronto, ON Research Associate I, Process Development Bachelors Exp: 0 to 2+ years |
BlueRock Therapeutics is seeking a Research Associate I, Process Development in Toronto, ON. As part of BlueRock's vision to change the future of medicine by enabling ground-breaking cell therapies, the successful candidate will be a key technical contributor to a dynamic and progressive team focused on developing novel therapeutics. The Research Associate II will be involved in hands-on work in developing and scaling cell and gene therapy manufacturing processes | 9/21/2022 |
| 6068 | Boston Analytical Salem, NH Analytical Chemist Bachelor’s degree in Chemistry or a related science discipline is required Exp: 0-2 years |
The Analytical Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 9/21/2022 |
| 6069 | Boston Analytical Salem, NH E&L Chemist I Bachelor’s degree in Chemistry or a related science discipline is required Exp: 0-2 years |
The Analytical Chemist conducts routine quantitative and qualitative analyses for Extractables & Leachables studies according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of extracts and pharmaceutical product samples using LC-MS, GC-MS, and/or ICP-MS. | 9/21/2022 |
| 6070 | Boston Analytical Salem, NH Microbiologist - QC BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. The schedule for this position is 1:00pm-11:30pm, Monday through Thursday. | 9/21/2022 |
| 6071 | Boston Analytical Salem, NH Microbiologist - Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. The schedule for this position is 1st shift, Wednesday through Saturday. | 09/21/2022 |
| 6072 | Boston Institute of Biotechnology Southborough, MA Research Associate / Scientist / Sr. Scientist – Downstream Process Development Bachelor’s degree in Biology or Chemistry related field; or MS degree in Biochemistry or Chemical Engineering Exp: BS: 0-10 years; MS: 0-5 years |
Essential requirements for this position include in-depth understanding and hands-on experience with recombinant protein purification from different expression hosts (including E. coli, Yeast, CHO and HEK) and an aptitude for careful, detail-oriented experimentation. The level of the position will be commensurate with the candidate’s experiences. | 09/21/2022 |
| 6073 | Boston Institute of Biotechnology Southborough, MA Upstream Process Development Research Associate BS degree in Biochemical Engineering or related field of study Exp: 0-2 years |
1. Set up, execute, and monitor microbial and mammalian cell culture production in fermenters and bioreactors. 2. Collect, record, and report experimental data. 3. Provide updates to a team lead on a regular basis. 4. Maintain all notebooks and documentation according to department standards. 5. Write SOPs, and batch records. 6. Ability to work well in a team environment and independently as required. | 09/21/2022 |
| 6074 | BostonGene Waltham, MA Research Associate, Molecular Biology and Next Generation Sequencing Bachelor’s (B.S.) degree in biology, clinical laboratory science, medical technology or related discipline Exp: 0-2 years |
BostonGene is seeking a highly motivated Junior Research Associate to join our R&D team in our laboratory located in Waltham, MA. This candidate will support BostonGene’s state-of-the-art primary next generation sequencing (NGS), adjunct analytical platforms, and automated analysis pipelines. The candidate will be expected to develop proficiencies in NGS support protocols, such as RNA and DNA isolation from tissue, cell free DNA isolation from plasma, Whole Exome Sequencing library preparation, RNA-Seq library preparation, qPCR, Molecular Biology techniques, and other sample QC techniques. | 09/21/2022 |
| 6075 | Boston Heart Diagnostics San Diego, CA Research Associate I in vivo Bachelor’s degree in life sciences or related discipline required. Exp: 0-2 years |
The successful candidate for the Research Associate I position will join the Beacon Discovery team with a multifaceted approach for providing high value services based on the Beacon Discovery platform and other proprietary technologies. The position provides an outstanding opportunity to learn new techniques and develop skills within a dynamic in vivo pharmacology research team. We work with multiple animal models, from anxiety to metabolism and beyond. If you are interested in working in a fast paced, challenging environment where you will have an opportunity to learn and succeed this may be the place for you. Laboratory experience with animal handling and pharmacology studies would be advantageous but is not necessary. Extensive training will be provided. | 09/21/2022 |
| 6076 | Boston Heart Diagnostics Foster City, CA HPLC Research Associate Bachelor's/Master’s degree Exp: BS: 0 - 3 years ; MS: 1+ year |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for HPLC Research Associates to support our Professional Scientific Services group in Foster City, CA. | 09/21/2022 |
| 6077 | Boston Heart Diagnostics San Diego, CA MSAT Research Associate B.S. degree in biological sciences, chemistry, biomedical engineering, immunology, or other related fields Exp: 1-2 years |
This individual will be responsible for performing release, in-process, stability, and process characterization testing for our PSS client’s Cell and Gene Therapy clinical development and commercial programs in a cGMP compliant manner working in the MSAT (Manufacturing Science and Technology) group. This position will perform all activities according to approved written procedures or protocols. Additional responsibilities may include revision to SOPs, method validations, method transfers, and comparability assessments or bridging activities with new analytical methods required for INDa and BLA. | 09/21/2022 |
| 6078 | Boston Heart Diagnostics Cambridge, MA Research Associate, Analytical Development Bachelor’s Degree/ Master’s Degree in related science. Exp: BS: 0-2+ years; MS: 0+ years |
Seeking an energetic and dependable analyst to perform routine testing to support process development and help progress programs through the pipeline. This individual will focus on molecular biology assays with a development opportunity to cross-train and support cell-based, potency, flow cytometry, separations and biophysical methods as well. This analyst will interface with many departments and projects necessary to complete tasks in a timely manner. | 09/21/2022 |
| 6079 | Boston Heart Diagnostics Cambridge, MA Research Associate (Separations + Biophysical) Bachelor’s Degree/ Master’s Degree in related science. Exp: BS: 0-2+ years; MS: 0+ years |
Provide timely internal non-GMP testing support for various teams; Support automation of analytical workflows and qualification of automated assays; Document lab work and results in ELN and/or LIMS; Coordinate, store, and properly handle samples and retains; Manage and track supply of controls, reference standards, and critical reagents; Train other analysts as necessary; Ensure Instruments and lab are properly maintained; Work with many other groups to support client's mission | 09/21/2022 |
| 6080 | PL Developments Copiague, NY Chemist I Chemist I Chemist I Bachelor’s degree in chemistry or related science from an accredited college or university Exp: up to 1 year |
Carry out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws. Complies with all current Good Laboratory Practices (cGLP), current Good Manufacturing Practices (cGMP), and safety requirements and laboratory Standard Operating Practices (SOPs). Conduct scheduled preventive maintenance and calibration of laboratory instrumentation (i.e., pH meter, HPLC, dissolution equipment, etc.). Prepare standard and sample solutions as required by the test methods. Operate general analytical instruments for all routine testing (i.e., HPLC, GC, UV, automatic titrator, and IR). Perform wet chemistry tests (i.e., LOD, pH, titration, etc.). | 9/13/2022 |
| 6081 | The Ritedose Corporation Columbia, SC Microbiologist I BS degree in Microbiology or related field Exp: 0 - 2 years |
The Microbiologist I is responsible for all duties related to performing environmental monitoring, personnel monitoring, microbial enumeration, microbial identification, media growth promotion, maintenance of microbial cultures, and sampling of utilities. The Microbiologist I is also responsible for performing all the microbiological testing related to raw materials, utilities, and in-process product testing. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. | 9/13/2022 |
| 6082 | Tanvex BioPharma San Diego, CA Research Associate, Cell Culture PPD - #1358 BS or advanced degree in chemical/biochemical engineering, cell biology, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Cell Culture Development is responsible for executing individual experiments related to all aspects of cell culture process development of biopharmaceuticals, including media preparation, bioreactor setup, cleaning, sterility and operation, maintaining instruments and equipment, examining data and preparing experiment reports. Applies basic engineering and scientific principles to perform trouble-shooting of processes, instrumentation, and equipment. | 9/14/2022 |
| 6083 | Tanvex BioPharma San Diego, CA Research Associate, Analytical Characterization - #1390 BS or advanced degree in analytical chemistry, chemical/biochemical engineering, biochemistry, or related disciplines. Exp: 0-3 years |
The Research Associate is a key member of the Analytical Characterization team and will be involved in supporting Tanvex’s CMC activities. The ideal candidate will have shown proficiency in hands-on analytical work and strong working knowledge in various physicochemical analyses for detailed characterization of recombinant protein therapeutics. Under the guidance of his/her supervisor, the candidate will help to develop and qualify analytical methods, and conduct characterization analysis to support regulatory filings, as well as provide analytical support for process development and method transfer activities. The candidate is also expected to be involved in drafting characterization study reports, Standard Operating Procedures, method development reports, method qualification protocols and reports, as well as to collaborate with other functional groups on significant technical matters. | 9/14/2022 |
| 6084 | Tanvex BioPharma San Diego, CA Research Associate, Analytical Chemistry Development - #1414 BS or advanced degree in chemical/biochemical engineering, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Analytical Chemistry Development is responsible for providing analytical chemistry support to research, process development, product development and manufacturing of biological therapeutics. Participate in analytical method development, characterization, qualification, validation as well as method transfer. Perform various analysis for characterization of biological therapeutics. | 9/15/2022 |
| 6085 | Tanvex BioPharma San Diego, CA QC Associate, Lab Control & Raw Material - #1346 Bachelor’s degree or advanced degree in chemistry, biology, biochemistry or related life sciences discipline Exp: 0-3 years’ |
The Quality Control Associate, Lab Control & Raw Materials is responsible for conducting routine and non-routine analyses of raw material and GMP product as assigned using appropriate analytical methods. This position will coordinate sampling, shipping, and testing of raw materials at outside contract laboratory and in-house to ensure data integrity and compliance, and will work with internal departments to ensure timely testing of raw materials for Manufacturing. The QC Associate will also perform assay transfers, validation of analytical methods, and testing product GMP samples as assigned, compile data for documentation of test procedures and preparation of reports, and ensure raw materials program is in compliance per internal SOP and CFRs. Knowledge of Laboratory Information Management System (LIMS) is a must. | 9/15/2022 |
| 6086 | Tanvex BioPharma San Diego, CA QC Associate, Validation and Tech Support - #1422 BS or advanced degree in chemistry, biology, biochemistry or related life sciences discipline. Exp: 0-3 years |
The Quality Control Associate, Validation and Tech Support is responsible for supporting the scheduling and maintenance of instruments and equipment in Quality Control. Additional responsibilities include assisting with transferring analytical test methods from development into the QC laboratory, performing feasibility studies, and executing method validations as well as conducting routine and non-routine analyses of GMP products as assigned by the manager. | 9/15/2022 |
| 6087 | Tanvex BioPharma San Diego, CA QC Associate, Lab Control and Raw Materials - #1355 BS or advanced degree in chemistry, biology, biochemistry or related life sciences discipline. Exp: 0-3 years’ |
The Quality Control Associate, Lab Control & Raw Materials is responsible for coordinating sampling, shipping, and testing of raw materials and products at outside contract laboratories and in-house. Additional responsibilities include updating compendial testing requirements (e.g. USP) of raw materials. Work with outside contract labs to ensure data integrity and compliance. Work with internal customers (e.g. Material Management) to ensure timely testing of raw materials for Manufacturing. Knowledge of Laboratory Information Management System (LIMS) is a must. | 9/15/2022 |
| 6088 | Advanced BioScience Labs Rockville, MD QC Microbiology I - (00325_COMPANY_1.4) B.A. or B.S. degree in microbiology, biology, or related scientific field Exp: 1-2 years |
The QC Microbiologist I will have several responsibilities in the QC group. The analyst will perform environmental monitoring (EM) for particulates and viables in support of cGMP manufacturing which includes several production suites of ISO class 5, 7, and 8 as well as EU Grade A to D in a GMP facility that produces biopharmaceuticals (vaccines, biologics, viral vaccines, monoclonal antibodies, etc.). In addition, monitoring of purified water, and compressed gases systems is required. Additional responsibilities may include EM data review and compilation of data, report writing, and trending of data; investigations, gowning training, and annual gowning qualification. | 9/15/2022 |
| 6089 | Advanced Cell Diagnostics Minneapolis, MN Research Associate, Microbiology QC Bachelor’s degree in Microbiology or a related scientific field or equivalent Exp: up to 3 years |
The responsibilities of this position are to participate in the Microbiology QC testing and reporting procedures: set up, read, and report the microbial QC bioburden and sterility testing of various sample types using culture methods that include direct plating, broth inoculation, and membrane filtration. Performance of environmental monitoring for viable microbes, particle counts, and WFI/deionized water testing, reading, and reporting. Assist with efficacy and validation testing, new procedure development, new equipment IQ/OQ and calibrations. Perform general lab duties, assist with sanitization of clean rooms, and additional duties as assigned. | 9/15/2022 |
| 6090 | Advanced Cell Diagnostics Minneapolis, MN Research Associate, Protein Development, Bioassay Bachelor’s degree in a related field Exp: up to 5 years |
We seek a highly motivated and creative individual to join our bioassay development team. This position is responsible for performing and developing bioassays using cytokines and antibodies to evaluate biological activity and to ensure quality products. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Participate in other projects and troubleshooting as needed. Perform additional duties as assigned. | 9/15/2022 |
| 6091 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, QC Analyst Masters in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 – 2 years |
Perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, SEC/HPLC, endotoxin assay, TOC, conductivity, pH, and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned. | 9/15/2022 |
| 6092 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate Master’s degree in a related field Exp: up to 2 years |
This position is responsible for participating in the development of Bio-Techne's various product lines. You will maintain knowledge of multiple products and procedures as well as draft and revise standard operating procedures in order to further the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 9/15/2022 |
| 6093 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Bioassay Protein Development Master’s degree in a related field Exp: up to 2 years |
We seek a highly motivated and creative individual to join our bioassay development team. This position is responsible for performing and developing bioassays using cytokines and antibodies to evaluate biological activity and to ensure quality products. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Participate in other projects and troubleshooting as needed. Perform additional duties as assigned. | 9/15/2022 |
| 6094 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in a related field Exp: up to 2 years |
The responsibilities of this position are to assist the protein product development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 9/15/2022 |
| 6095 | Acessa Health San Diego, CA Research Associate 2 M.S. Molecular Biology, Chemistry, Biochemistry or related field. Exp: 1 year |
Hologic is seeking a Research Associate 2 responsible for automated synthesis of oligonucleotides, purification of oligonucleotides by chromatographic and gel electrophoretic techniques, and characterization of oligonucleotides by a variety of physicochemical techniques. The Research Associate will also participate in basic research projects exploiting novel properties of oligonucleotides in diagnostic assays. This position will also be expected to maintain accurate records of oligonucleotide synthesis and to design and interpret experiments related to the use of novel oligonucleotides in diagnostic assays. | 9/15/2022 |
| 6096 | Agena Bioscience San Diego, CA Research Associate II - Assays by Agena Bachelor’s degree in biology, chemistry or related Exp: 1-3 years’ |
The Research Associate II position is a laboratory-based role. It is part of the Assays by Agena (AbA) team, and under the direct supervision of a Scientist. In this role, you will work on custom assay development for multiplexed panels for detection on Agena Bioscience’s MassARRAY® platform. | 9/15/2022 |
| 6097 | Agenus Berkeley, CA Process Development Research Associate Bachelor’s degree or native equivalent in Biochemistry, Biology, Biotechnology, Cell Biology, Chemistry, Chemical Engineering or a related field Exp: 0-2+ years |
This position will primarily focus on conducting CHO cell culture evaluation and process development in shake flasks and bench scale bioreactors. The successful candidate will be involved in upstream process development of our pipeline programs, including clone evaluation, process parameter optimization, and generation of material to support downstream and analytical development. Strong aseptic techniques and laboratory skills and experience in mammalian cell culture procedures is preferred. Will require some weekend/off-shift work, as needed. | 9/15/2022 |
| 6098 | Agenus Lexington, MA Research Associate - Research & Discovery BS or MS degree in immunology, molecular and cell biology, or related discipline Exp: 1+ years |
Agenus (Lexington, MA) is looking for a talented and highly motivated Research Associate to join our Biomarkers group. The successful candidate is expected to contribute to the discovery, research, and development of novel immunotherapeutic agents to address unmet medical needs of cancer patients. She/he will have opportunities to grow their career through acquisition of new skills, experiences, and professional relationships in a fast-paced and resource-rich environment. Our collaborative and interdisciplinary research team has a track-record of applying state-of-the-art technologies and innovative methodologies to advance cutting-edge immune-oncology (IO) medicines into the clinic. | 9/15/2022 |
| 6099 | Ajinomoto Bio-Pharma Services San Diego, CA Microbiology Technician - 1st Shift Bachelors degree preferred in a Life Sciences discipline or equivalent. Exp: Zero to two (0-2) years |
We are currently seeking an Microbiology Technician to support Ajinomoto Bio-Pharma Services manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 9/15/2022 |
| 6100 | Ajinomoto Bio-Pharma Services San Diego, CA Microbiology Technician - 2nd Shift Bachelors degree preferred in a Life Sciences discipline or equivalent. Exp: Zero to two (0-2) years |
We are currently seeking an Microbiology Technician to support Ajinomoto Bio-Pharma Services manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 9/15/2022 |
| 6101 | Alexion Pharmaceuticals New Haven, CT Engineer I, Device Development Bachelor’s degree in Engineering (Biomedical, Chemical, Mechanical, or Electrical Engineering) Exp: 1 to 3 year |
This position will serve the role of Engineer I for device development of Alexion products including continuous product improvement within the Development function of Alexion. The candidate will support technical design and development activities for device and combination products and assist the technology transfer. | 9/15/2022 |
| 6102 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Injectable Drug Product Development MS in Pharmaceutical Sciences, Chemistry, Biochemistry, Biophysics, Chemical engineering, or relevant field. Exp: 0 to 1 years |
The position is required to join Injectable Drug Product Development group of Alexion-AstraZeneca Rare Disease pharmaceuticals’ Pharmaceutical Development and Clinical Supply (PDCS) department. The job entails experimental work on various aspects of drug product characterization, including formulation development, in use compatibility studies for intravenous and subcutaneous administration, process development to support drug product manufacturing support, and particulates testing. The position entails execution of the studies and data processing and compiling to generate and support development reports as well as other required documentation. Solid understanding of assay development and bioprocess is highly preferred. Hands-on experience with biotherapeutics development, including detailed understanding product lifecycle, and current regulations for product administration, is highly desirable. In addition, this position is expected to interact regularly with scientific staff within the department and in some cases with colleagues in other departments (e.g., Analytical Sciences, Device development, Biologics Drug Substance Process Development) The ability to accurately and independently generate procedures, protocols, reports, and CMC section content for regulatory filings pertaining to drug product is a requirement of this position. | 9/15/2022 |
| 6103 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Small Molecule DMPK Master or equivalent degree in chemistry, biochemistry, biology or any other disciplines related to pharmaceutical sciences Exp: 0-2 years |
The Small Molecule Drug Metabolism and Pharmacokinetics (DMPK) team of Alexion, AstraZenica Rare Desease, is seeking an associate scientist to support drug metabolism studies in discovery and early development. | 9/15/2022 |
| 6104 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, IVIVP MS Exp: 0-2 years |
We are seeking a highly motivated in vivo pharmacologist to work in a dynamic preclinical environment focused on delivering clinically translatable solutions to advancing drug development. The full-time role will focus on the design, development, and evaluation of lead therapeutics in nonclinical pharmacology studies and ex vivo biochemical and bioanalytical assays support. The successful candidate will contribute to development and characterization of in vivo mouse models, as well as support ex vivo protein and cellular analysis. | 9/15/2022 |
| 6105 | American Regent New Albany, OH R&D Analytical Chemist R&D Analytical Chemist B.S. in Chemistry or equivalent education required. Exp: 1 year |
This R&D position will be responsible for testing of raw materials, finished products, and stability samples using existing analytical methods and wet chemistry. | 9/16/2022 |
| 6106 | American Regent New Albany, OH Validation Engineer I Validation Engineer I Bachelor’s Degree in Life Sciences, Engineering or equivalent required. Exp: 1 year |
The Validation Engineer I will develop and execute validation protocols and reports that support the business needs of the company. The position will support the qualification and validation of the pharmaceutical manufacturing processes and ensure that the facility, systems and processes perform according to internal specifications, comply with current GMPs and are maintained in a validated state. | 9/16/2022 |
| 6107 | Ampac Analytical Rancho Cordova, CA Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Bachelor’s degree in Chemistry or an appropriate science required. Exp: One (1) to two (2) years |
Must use independent judgment to analyze and make determinations as to the quality of a product, using analytical equipment pertinent to the appropriate application of skills. Use various laboratory procedures related to analysis of bulk and pharmaceutical chemicals. Perform analysis of samples using various laboratory equipment and techniques such as FT-IR, Loss On Drying, Non-volatile Residue, Titrations, moisture analysis by Karl Fischer, in addition to other methods. Operate LC and GC systems in order to complete analyses of various types of samples. Maintain a thorough and neat laboratory notebook. Troubleshoot fixes for various instruments in the laboratory. May perform peer review of various commercial product laboratory data. | 9/16/2022 |
| 6108 | Ampac Analytical Rancho Cordova, CA Process Engineer Bachelor's of Science Degree in Chemical Engineering required. Exp: One to three years |
We are looking for enthusiastic Chemical Engineers to join our Process Engineering Team! We have several opportunities at our Rancho Cordova, CA location (Greater Sacramento Area). We will pay for your relocation!! | 9/16/2022 |
| 6109 | Ansa Biotechnologies Emeryville, CA Research Associate / Senior Research Associate, Downstream Process Development Bachelor’s/Master’s Exp: 0-4 years |
Execute downstream processing workflow for recombinant protein production: E. coli harvest, lysis, clarification, purification, and buffer production Keep detailed notes of experimental procedures and observations using an electronic lab notebook Collaborating in a team environment: At Ansa, communication between teams is critical–our technology is built on enzymes, chemistry, and automation. Additionally, we believe that kind-natured honesty and openness are an instrumental part of the scientific endeavor. | 9/16/2022 |
| 6110 | Arbor Biotechnologies Cambridge, MA RA/SRA, Protein Engineering Bachelor’s degree in molecular biology, biochemistry, or a related field Exp: 1-3 years |
The Protein Engineering Team is looking for a RA/SRA to join our cross-functional team and contribute to the discovery and development of novel gene editing systems. This role affords the opportunity to hone molecular biology techniques and help develop new assays and methods in a fast-paced environment all while making a broad impact on Arbor’s productivity and portfolio. The ideal candidate will have hands-on experience in the wet laboratory, an appetite for learning a wide variety of topics, excellent organizational skills, attention to details, and the ability and self-motivation to work independently. | 9/16/2022 |
| 6111 | Arbor Biotechnologies Cambridge, MA Research Associate/Senior Research Associate, Non-Viral Gene Therapy BS/MS or equivalent in Chemical/Biomedical/Biochemical Engineering, Bioengineering, Chemistry, Biochemistry, Pharmaceutical Sciences or a related fiel Exp: 1-3 years |
The Senior Research Associate/Research Associate will support our LNP formulation pipelines and in vitro/in vivo preclinical requirements through the design and execution of experiments to help screen and produce various non-viral formulations enabling the encapsulation of various RNA entities. This candidate will also help support various characterization assays for the various formulations as needed. The ideal candidate for this position will be a motivated and proactive individual with a passion for nanomedicinal/LNP formulations and processes. The applicant should have strong wet laboratory, communication and collaboration skills preferably with a background in the appropriate formulation deliverables. This role will have no supervisory responsibilities and will report to the Principal Scientist, Non-Viral Gene Therapy. | 9/16/2022 |
| 6112 | ArcherDx San Francisco, CA Clinical Laboratory Technician - Tissue Culture BS in Cell Biology, Molecular Biology, Biochemistry, or equivalent Exp: 1+ years |
We are looking for a versatile, detail oriented Tissue Culture Technologist to join our San Francisco laboratory who can, with minimum supervision, perform cell culturing and microscopic analysis. | 9/16/2022 |
| 6113 | ArcherDx San Francisco, CA DNA Extraction Technician Bachelor’s degree in clinical laboratory studies or equivalent science related studies Exp: 1+ years |
We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work at our San Francisco location as well as ability to work overtime and off-schedule days as needed. | 9/16/2022 |
| 6114 | ArcherDx San Francisco, CA Engineering Technician Bachelor degree in an engineering or science field preferred Exp: 1 – 2 years |
We are looking for a passionate and driven Engineering Technician to join our Equipment Engineering Team who can come in and own the day to day equipment tasks which maintain regulatory compliance, equipment states and a high functioning lab environment. This individual will be able to seamlessly interface with production and engineering teams to drive forward task completion. | 9/16/2022 |
| 6115 | ArcherDx Iselin, NJ Extraction Technician Bachelor’s or Master's degree in Medical Technology, Biology, Chemistry, Biochemistry or related life science Exp: 1 years |
Our Iselin (Metropark), NJ operations team is looking for a passionate and focused Extraction Laboratory Technician I to join invitae and support high-complexity laboratory testing on patient specimens across various assays and platforms. The extraction team member will partner with the Extractions Lead to continuously improve daily extraction operations at our Metropark Laboratory. | 9/16/2022 |
| 6116 | ArcherDx San Francisco, CA Clinical Laboratory Scientists - I, II, III, or IV Bachelor's degree in clinical laboratory studies or equivalent science related studies. Possess an active, valid license (Generalist or CGMBS) issued Exp: 1+ years |
We are looking for a motivated and self-driven Clinical Laboratory Scientist to join our team. This role will be responsible for performing high complexity diagnostic testing on patient specimens across various molecular assays and platforms (Including NGS, NIPS, aCGH, MLPA, ddPCR, Genotyping, Sanger and Long Range Sequencing). This role envelopes all steps from specimen processing to data analysis; performing quality control and assurance procedures, while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, strong written and verbal communication skills, and the ability to multitask as well as work independently within a team environment. | 9/16/2022 |
| 6117 | Arcturus Therapeutics San Diego, CA Research Associate I/II MS/BS degree in biochemistry, biological sciences, pharmaceutical sciences, chemistry, chemical engineering, molecular biology, or other relevant disc Exp: 1 to 5 years |
Arcturus is seeking a Research Associate to join our RNA team. This individual will work with a team of highly-motivated scientists to advance development projects within RNA production, RNA process development, RNA formulations, and analytical sciences. | 9/16/2022 |
| 6118 | Arcturus Therapeutics San Diego, CA Research Assistant/Research Associate I, Analytical Development Bachelor’s degree in Chemistry, Biochemistry, Molecular Biology, Pharmaceutical, Life Science or equivalent. Exp: Zero to two (0-2) years |
The Research Associate, Analytical Development will be responsible for conducting routine analytical characterization of RNA drug substances, intermediates and formulated drug products to support an emerging research pipeline focused on treating rare diseases. The candidate will also assist with optimization, development and implementation of new analytical procedures as needed. | 9/16/2022 |
| 6119 | Arrowhead Pharmaceuticals San Diego, CA Research Associate, Biology (In Vitro) BS in Biology, Physiology, Pharmacology, or relevant area Exp: 0-2 years |
Arrowhead is seeking a Research Associate to join our growing Biology Department at San Diego site. This is an excellent opportunity to utilize, contribute and advance the ideal candidate’s laboratory skills in a progressive, state-of-the-art and diverse facility. | 9/16/2022 |
| 6120 | Xencor Monrovia, CA Research Associate 1 Research Associate 1 Research Associate 1 Bachelor’s degree in biological sciences, cell biology, immunology or a related field is preferred. Exp: 1 years |
Responsible for contributing to daily laboratory operations in support of the identification of therapeutic antibody candidates using specialized methods specific to the assigned group, function or department. | 9/6/2022 |
| 6121 | Xencor Monrovia, CA Research Associate 1 BS in cell biology, immunology or related field; MS is highly preferred. Exp: 1 year |
We currently have an excellent opportunity for a talented Research Associate 1 to join our team! Job Duties Include: Grow and maintain mammalian cell lines Mammalian protein expression and plasmid DNA purification Performs primary mammalian tissue culture Maintains tissue cultures including mammalian primary cells and cell lines Coordinate and collaborate tasks across multiple groups, aligning with molecular biology and protein purification Documents experimental protocols, designs, and results in a laboratory notebook Employs computer programs to collect and analyze data Performs other duties as required | 9/6/2022 |
| 6122 | Zymo Research Irvine, CA Bioinformatics Associate Master or bachelor's degree in Biology, Bioinformatics, Computer Science, Mathematics, Statistics, or a related discipline. Exp: 1 to 3 or more years |
Zymo Research is seeking a Bioinformatics Associate to join our Bioinformatics team. The qualified individual will play a key role in building, maintaining, and executing data-analysis pipelines for Next-Generation Sequencing methods to support Zymo Research’s global product strategy. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you | 9/7/2022 |
| 6123 | Zymo Research Irvine, CA Research Associate – Protein Engineering Group MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field, developing recombinant proteins and peptides production methods. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 9/7/2022 |
| 6124 | Zymo Research Irvine, CA Research Associate MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field, developing recombinant proteins and peptides production methods. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 9/7/2022 |
| 6125 | Zymo Research Irvine, CA Research Associate – Assay Development MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 9/7/2022 |
| 6126 | Zymo Research Irvine, CA Research Associate (RNA Seq team) MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field specifically in the cutting-edge technologies of next-generation sequencing (NGS) and nucleic acids handling. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 9/7/2022 |
| 6127 | Zymo Research Tustin, CA Laboratory Technician/QC Associate BS degree in Biochemistry, Microbiology, Genetics, Immunology, Virology, Molecular Biology or related field. Exp: 1-2 years |
Assist in the manufacturing of various chemicals, buffers, and other product-related components to ensure consistent product performance. Responsible for conducting quality control tests on various chemicals, buffers, and other product-related components. | 9/7/2022 |
| 6128 | Accelerate Diagnostics Tucson, AZ Research Associate, Core Lab (2nd Shift) Bachelor of Science degree in Microbiology, Molecular Biology, or related life sciences. Exp: 1 year |
The shift for this position is Monday - Friday, 2:00pm – 11:00pm. The Research Associate is responsible for the routine execution of experiments supporting assay development, technical operations, and core lab. This position can be in different teams including assay development, core lab and technical operations depending upon business needs. | 9/7/2022 |
| 6129 | Affinivax Cambridge, MA QC Analyst 1 - Vaccine Development Bachelor/Master of Science in Biology, Molecular Biology, Biochemistry, Chemistry, Analytical Chemistry Exp: 1+ years |
Affinivax is currently seeking a motivated QC Analyst to join our Quality Control Team to support and contribute to our development efforts and ongoing clinical trial. | 9/8/2022 |
| 6130 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 9/8/2022 |
| 6131 | Sciecure Pharma Monmouth Junction, NJ Project Coordinator Bachelor’s degree in Life Science (Biology, Chemistry, Chemical Engineering, Etc.). Exp: 1 – 3 years |
Sciecure Pharma Inc. specializes in the research and development of pharmaceutical finished products from conception to commercial. Our growing company is seeking to hire a project coordinator who will be in charge of assisting in organizing our ongoing projects. This task involves monitoring project plans, schedules, organizing and participating in stakeholder meetings, and ensuring that project deadlines are met in a timely manner. To be successful as a project coordinator, you will need to be able to work on tight deadlines, be competent in using Microsoft Office applications such as Word and Excel, and have exceptional verbal, written, and presentation skills. A bachelor’s degree in life science is required for consideration. | 9/8/2022 |
| 6132 | Spriaso Salt Lake City, UT Research Chemists Bachelor's degree in chemistry, chemical engineering, biochemistry, or other related degree concentration Exp: one year |
These positions entails doing product, process, and analytical functions in support of product and technology development under direction of product development and/or analytical leader. | 9/9/2022 |
| 6133 | Tanabe Research San Diego, CA Research Associate I/II – Oncology BS in a biology-related field such as Cell Biology, Molecular Biology, Immunology, Biochemistry, etc. Exp: 0-2 years |
An entry level Research Associate for our Oncology department to conduct biological studies using standard to advanced cell biology and immunological techniques. | 9/9/2022 |
| 6134 | Vaxess Technologies Cambridge, MA Research Associate, Bioassays Bachelor’s or Master’s degree in Life Sciences Exp: 1-2 years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials sciences, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in bioassays to join our core team of scientists and engineers. This is a unique opportunity to be part of an emerging early phase clinical company bringing innovative technology to the global market. | 9/9/2022 |
| 6135 | Vaxess Technologies Cambridge, MA Research Associate / Senior Research Associate, Formulation and Analytical DevelopmentResearch Associate / Senior Research Associate, Formulation and Master’s degree in one of the Life Sciences, Chemistry, Pharmaceutical Sciences, Chemical Engineering or Biomedical Engineering Master’s degree in one Exp: 0-2+ years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials sciences, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in formulation and analytical development to join our core team of scientists and engineers. This is a unique opportunity to be part of an emerging early phase clinical company bringing innovative technology to the global market. | 9/9/2022 |
| 6136 | Aesculap Irvine, CA QC Chemistry Associate II (Chemical Chromatography) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 9/9/2022 |
| 6137 | Aesculap Irvine, CA QC Chemistry Associate II (In Process Chemistry) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 9/9/2022 |
| 6138 | Aesculap Irvine, CA Quality Operations Associate II Bachelor's degree in a Science related field preferred. Exp: 01 – 02 years |
The Quality Operations Associate II under a moderate degree of supervision is responsible for performing incoming and in-process inspection (visual, functional and dimensional) using qualified instruments. This position will also be responsible for reviewing data, certificate of compliance and performing materials release as required. | 9/9/2022 |
| 6139 | AGC Biologics Longmont, CO QC Associate I/II, Microbiology Degree in Microbiology, biology or other scientific discipline Exp: 0-2+ years |
The Microbiology Associate I/II will be part of the Longmont Quality Control Microbiology Department. This individual will be responsible for the testing and support of the Microbiology Laboratory in support of a cell and gene therapy Contract Manufacturing facility. Responsibilities include routine Quality Control laboratory activities in support of GMP testing, and execution of laboratory maintenance activities. | 9/9/2022 |
| 6140 | AGC Biologics Boulder, CO Manufacturing Associate I-III BS in Chemistry, Biology or other relevant discipline. Exp: 1-7 years |
The Manufacturing Associate I-III performs GMP manufacturing operations safely, reliably and in compliance with stated processes. We offer a dynamic environment, innovation, operational excellence, and career growth. | 9/9/2022 |
| 6141 | Amphastar Pharmaceuticals Inland Empire, CA Microbiologist Bachelor's degree from four-year college or university in biology or related field Exp: one to two years |
A Pharmaceutical Manufacturing company is looking for the talents of a Microbiologist to perform a variety of tests which directly or indirectly affect product release, and test for the sterile quality of products manufactured by performing the following duties. | 9/9/2022 |
| 6142 | Amphastar Pharmaceuticals Rancho Cucamonga, CA In Vitro Bioassay Analyst Bachelor's degree in biochemistry, biology, molecular biology or other related degree concentration (required). MS in biochemistry, biology, molecular Exp: one year |
The in vitro bioassay analyst is an entry level role and will be responsible for assisting in the development and qualification of cell-based potency and ELISA/immunology-based drug products. They will also be responsible for the on-time release and stability of raw materials, in-process, finished pharmaceutical drug substances and drug product and non-routine testing of drug product in a cGMP environment. | 9/9/2022 |
| 6143 | Amphastar Pharmaceuticals Rancho Cucamonga, CA Process Technology Development Engineer Bachelor's degree (Bachelor of Science) from a four-year College or University in Chemical Engineering or other relevant scientific field. Exp: One to two years |
The Process Technology Development Engineer researches and evaluates new technology and design related to new equipment, process scale up and process improvement. Identify critical to quality attributes of the process and perform experiments to study the process control with the aim of optimizing the process at various stages in its product life cycle. Achieves the corporate target and ensure smooth process development and transfer for the commercial scale production. . | 9/9/2022 |
| 6144 | Amphastar Pharmaceuticals Rancho Cucamonga, CA Maintenance Engineer Bachelor's degree (B.S.) from four-year college or university in Mechanical or Electrical engineering or other relevant scientific field. Exp: 6 months |
Perform setup, maintenance and operation of aseptic and non-aseptic production equipment along with general facility repair and maintenance. | 9/9/2022 |
| 6145 | Nitto Denka Avecia Cincinnati , OH Quality Assurance Specialist Quality Assurance Specialist BS/BA in science Exp: 1-3 years |
Acts as departmental resource for cGMP programs Writes SOP’s compliance documents for cGMP program. Reviews and authorizes batch production records and quality control documentation. Performs compliance audits of suppliers, contract labs and vendors then writes audit reports. Performs internal audits and ensures observations are corrected. Sets-up and tracks material flow and material-labeling process to ensure compliance with cGMP program Trains staff in area of cGMP and maintains training records | 9/9/2022 |
| 6146 | Nitto Denka Avecia Milford, MA Quality Control Environmental Analyst I Quality Control Environmental Analyst I BS in chemistry, biology or related discipline or equivalent combination of education and experience Exp: 0-2 years |
Purpose of Position: The QC Environmental Analyst I supports manufacturing operations by performing environmental monitoring of the cleanrooms, and sampling and testing of the water system, as well as perform additional microbial sampling and testing as required. The position works within the QC lab on assigned tasks following written procedures and protocols. The position also assists in the maintenance of overall laboratory systems. | 9/9/2022 |
| 6147 | Nitto Denka Avecia Milford, MA Quality Control Analyst I (2nd Shift) BS in chemistry, biology or related discipline or equivalent combination of education and experience Exp: 0-2 years |
Purpose of Position: The QC Analyst I is responsible for conducting routing analysis of raw materials, in-process samples and finished products in a strict GMP setting. The position involves working in the QC laboratory and in the manufacturing space on assigned tasks following written procedures and verbal instructions. | 9/9/2022 |
| 6148 | Nitto Denka Avecia Milford, MA Research Chemist Research Chemist BA/BS/MS Exp: BA/BS: 1+ yrs.; MS : 0+ yrs. |
The Research Chemist is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides | 9/9/2022 |
| 6149 | Avidity Biosciences San Diego, CA RESEARCH ASSOCIATE, BIOANALYTICAL BS or MS in Biology, Biochemistry, or related discipline Exp: 1 year |
We are seeking a Research Associate focused on bioanalysis to join the Bioanalysis team at Avidity Biosciences in La Jolla, CA. This position will require hands-on lab work with responsibility for processing and analyzing animal blood and tissues. The ideal candidate will be able to assist in the development of novel methods for quantifying antibodies and oligonucleotides in complex biological matrices. The ideal candidate is expected to be a strong team player who enjoys scientific discovery and can communicate and collaborate in a fast-paced interdisciplinary environment. Title and compensation will be commensurate with the candidate’s experiences. | 9/9/2022 |
| 6150 | Avidity Biosciences La Jolla, CA RESEARCH ASSOCIATE, IMMUNOLOGY B.S./B.A. degree in the biological sciences Exp: 1-2 years |
Avidity is seeking an enthusiastic and dedicated Research Associate to join our Discovery Biology team who can assist with ongoing studies that aim to expand our AOC platform. This is a hands-on research position, and a successful candidate will have a proven record of producing exceptional results in a laboratory setting. | 9/9/2022 |
| 6151 | Bio-Concept Laboratories Boston, MA Associate Scientist I - Boston, MA (Entry Level) Recent Bachelor’s degree in chemistry, biochemistry or related field. Exp: Entry Level |
We are seeking a talented and self-motivated scientist (recent graduate or upcoming graduate) who is eager to be part of our success, and who embraces our core values: Integrity, Excellence, and Teamwork. This role requires scientific curiosity, willingness and eagerness to learn and support drug development efforts. If you have a passion for hands-on problem solving to develop cutting-edge pharmaceuticals, this is the job for you! Working in a dynamic, fast-paced, team-oriented and collaborative environment at Pace Analytical Life Sciences! | 9/9/2022 |
| 6152 | Biomarker Strategies Rockville, MD Technician or Research Assistant (Part-time positions considered) Academic qualifications not listed. Exp: 1+ years |
BioMarker Strategies seeks highly motivated laboratory personnel who will assist in the development of a commercialization-focused cancer diagnostic system. Candidates will be responsible for performing research and development experiments, and to be able to summarize experiments and results. This position is a wet lab position and candidate will predominately perform work at the bench. | 9/9/2022 |
| 6153 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 9/9/2022 |
| 6154 | CRISPR Therapeutics San Francisco, CA Research Associate I/II, CRISPRx BS in biology or related discipline Exp: 0-3 years |
We are seeking a Research Associate I/II to join the CRISPRx group at CRISPR Therapeutics, the leading gene editing company. The successful candidate will be an integral part of a team whose aim is to advance next generation gene editing. The position requires enthusiasm, passion, attention to detail and a desire to assist in developing the next generation of gene editing. | 9/9/2022 |
| 6155 | Ferndale Pharma Group Ferndale , MI Microbiologist Bachelor’s degree in Microbiology or a closely related field, or an equivalent combination of education and experience. Exp: One year or more |
Carries out routine day-to-day microbiological testing of Water, Raw Materials, Bulk and Finished Products and Stability samples in the Microbiology Laboratory. Performs routine microbiology testing, such as pour plate methods, membrane filtration, Preservative Effective Testing, and isolation and identification of organisms. | 9/9/2022 |
| 6156 | Ferndale Pharma Group Ferndale , MI Chemist Bachelor of Science in Chemistry or a closely related field or an equivalent combination of education and experience. Exp: one to two years |
Carry out routine day-to-day quality control testing of Water, Raw Materials, Bulk, Finished Products and Stability samples in the Quality Control Laboratory. Perform routine chemical testing by such means as HPLC, GC, FTIR, UV Spectrophotometry, Titrations and other physical and chemical techniques. Review note books and generate test data reports. Write and revise SOPs. Prepare protocols, perform testing for special investigations and write scientific reports. | 9/9/2022 |
| 6157 | Cellular Technology Limited Cleveland, OH Laboratory Assistant Bachelor of Science degree. Exp: one year |
We are seeking a highly motivated Laboratory Assistant for our Contract Research Laboratory who will perform immunology testing of client specimens collected from both pre-clinical and clinical studies using the following test methods: ELISPOT, ELISA, flow cytometry, etc. All work is performed according to general laboratory safety standards, internal standard operating procedures (SOPs), client protocols, and applicable international, federal and state regulations. | 9/9/2022 |
| 6158 | Lampire Biological Labs Pipersville, PA CELL CULTURE TECHNICIAN Bachelor's Degree in a scientific field preferred. Exp: 0-2years |
Scope of Responsibility: To perform cell culture and cell banking activities such as Hybridoma development and growing of monoclonal cells in culture and to document activities accurately at Lampire with the goal of providing consistent, high-quality products and services to our customers with complete, accurate documentation. | 9/9/2022 |
| 6159 | Lampire Biological Labs Pipersville, PA LABORATORY ANIMAL TECHNICIAN Bachelor’s Degree in a scientific field preferred Exp: 0-2years |
Job Description: The project related functions for the small lab animals, including but not limited to mice, rats, guinea pigs, and hamsters. This person will be responsible for preparing and administering injections, performing bleeds, processing bleeds and updating records as needed. To perform animal procedures as the project dictates on small laboratory animals and input data at Lampire with the goal of providing consistent, high quality products and services to our customers with complete, accurate documentation. | 9/9/2022 |
| 6160 | Sofregen Medical Framingham, MA Quality Engineer Bachelor’s degree in scientific discipline Exp: 0-2 years |
Sofregen Medical is seeking a Quality Engineer to join our Manufacturing team and support the production of Sofregen’s commercial silk-based medical device platform. The Quality Engineer plays a vital role in the maintenance of the Quality Management System as well as the daily operation of the laboratory. Duties will include maintaining a system to track equipment calibration & maintenance, environmental monitoring, inventory management, receiving and incoming inspection, and authoring routine Quality Control documentation (e.g. deviations, standard operating procedures (SOPs), batch records, etc.). The Quality Engineer will further collaborate with Manufacturing members to provide general support to critical processes. | 8/29/2022 |
| 6161 | Sound Biologics Bothell, WA ASSOCIATE SCIENTIST/SR. ASSOC. SCIENTIST BS or MS degree in analytical chemistry, biochemistry, chemical engineering, or a similar discipline Exp: 1+ years |
Sound Biologics is seeking analytical development and characterization scientist to participate in the R&D activities from preclinical studies, process development, through GMP production and IND filings. This is a unique opportunity for a motivated scientist to contribute experimentally, as well as intellectually, in advancing our mission in a supportive, but fast-paced team setting. | 8/29/2022 |
| 6162 | Spherotech Lake Forest, IL Quality Control Associate Bachelor's degree in Chemistry or related field Exp: 1 year |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. | 8/29/2022 |
| 6163 | Spotlight Therapeutics Hayward, CA Research Associate (RA) - Protein Engineering BS/MS in Biochemistry, Molecular Biology, Genetics, or related field Exp: 1-2 years |
We are seeking a biochemist/molecular biologist to join our Platform Technology group. Our group is building a new class of biologics from a toolbox of CRISPR/Cas systems, affinity domains, and cytosolic delivery technologies. In this role, the candidate would design novel RNPs and optimize therapeutic properties such as stability and editing efficiency, using both protein and RNA engineering. This position is an outstanding opportunity to contribute directly to our core protein engineering and production capabilities, as well as work directly with our cell biologists, immunologists, and gene editing experts. Primary responsibilities will include several aspects of protein engineering, such as plasmid construct design, protein expression, and purification. In addition, biochemical assays would be carried out to assess purity, concentration, stability, integrity, and enzymatic activity of RNPs. | 8/29/2022 |
| 6164 | Stability Biologics San Antonio, TX QA Specialist - San Antonio, TX BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.) Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 8/29/2022 |
| 6165 | StageBio Marlboro, MA Laboratory Imaging Specialist (Preclinical CRO) College degree preferred (in a technical major like electrical, imaging, computer, biomedical engineering) Exp: 1-2 years’ |
StageBio is seeking a full-time Imaging Specialist to join our Marlborough, MA facility. | 8/29/2022 |
| 6166 | StellarTech Research Milpitas, CA Quality Engineer II BS degree or equivalent. Exp: 1-3 years |
Stellartech is looking for a Quality Engineer to join our Team. | 8/29/2022 |
| 6167 | SteriPharma Syracuse, NY Microbiology Analyst, 2nd Shift, Pharma Bachelor’s degree from a regionally accredited institution in science or related field. Exp: 1-3 years’ |
This position performs environmental monitoring and quality control of aseptic process area, to include testing of finished products, raw materials, and components according to established procedures. Position reviews records for accuracy. Position applies standard concepts, practices, and procedures within the laboratory. | 8/29/2022 |
| 6168 | Strand Therapeutics Boston, MA Associate Scientist/Sr Associate Scientist, Bioanalytical M.S. in Biology, Immunology, Biochemistry, Pharmacology, or a related field. Exp: 1-3 years |
Strand’s Bioanalytical Sciences team is looking for a Boston-based Associate Scientist/Sr Associate Scientist with hands-on experience in bioassay development. The individual in this role will support discovery & development programs through the development and execution of bioanalytical assays and by interfacing with internal & external stakeholders. The individual will work with scientists within the Bioanalytical Sciences team, broader Nonclinical group, and other functional groups to ensure that only the highest quality data is generated by our team. The successful candidate must have experience in assay development and specifically hands-on experience executing ELISA (& MSD), Luminex, qPCR/RT-qPCR, flow cytometry and other bioanalytical assays. The candidate must have integrity, be respectful and courteous, have a collaborative spirit, and come ready to make an immediate impact. | 8/30/2022 |
| 6169 | Strand Therapeutics Boston, MA Associate Scientist, mRNA Process Development BS in Biochemistry, Chemical Engineering, Molecular Biology, Bioengineering, Molecular Medicine, Genetics or related field preferred. Exp: 1-2+ years |
We are looking for a highly motivated and innovative candidate for the role of Associate Scientist, mRNA Process Development. The expectation is that the Associate Scientist will have experience independently executing mRNA process development experiments and production efforts. Reporting to Scientist, Process Development, the right candidate will be a strategic thinker that brings a leadership presence and enthusiasm for Strand along with a desire to conquer new challenges. | 8/30/2022 |
| 6170 | Strand Therapeutics Boston, MA Research Technician B.S. Exp: 0.5-1 years |
We are looking for a highly motivated and innovative candidate for the role of Research Technician. Reporting to the Sr Scientist of Vector Engineering, this individual will provide support to various R&D teams to help streamline daily research operations. The ideal candidate will have experience with mammalian cell culture, media preparation, cell line maintenance and reagent/inventory management of lab essentials. The candidate will be expected to work in an innovative, fast-paced, cross-collaborative biotech environment and contribute to multi-disciplinary team activities to advance our platform. | 8/30/2022 |
| 6171 | Sutro Biopharma San Carlos, CA Associate Engineer / Engineer, MSAT (San Carlos, CA) BS or MS in Chemical/Biochemical Engineering, or Biological Sciences, or relevant field. Exp: Associate Engineer: 0 – 3 years |
Sutro Biopharma, Inc. is looking for an energetic and talented professional to join its MSAT Group. MSAT Group responsible for technology transfers, manufacturing support (investigations, change controls, CAPAs, process capability/monitoring/capacity/efficiency/quality improvements) and process validation. We are dedicated to making a difference in the lives of patients, both as individuals and as part of a team. The position will be based in Sutro’s, San Carlos, CA Manufacturing site. | 8/30/2022 |
| 6172 | Sword Diagnostics Chicago, IL Research Associate I BS or BA in biology, biochemistry or related field Exp: one to three (1 - 3) years |
Job Responsibilities: • Plan experiments with guidance from supervisor • Perform complex and critical laboratory experiments (primarily ELISA) with accuracy and precision • Analyze experiment results and recommend potential follow-on experiments • Follow all established company processes and procedures • Prepare buffers and other chemical solutions as needed • Other duties and responsibilities as assigned | 8/30/2022 |
| 6173 | TechLab Blacksburg, VA Research Technician B.A. or B.S. in a life science Exp: 1 year |
Job Summary The job of the Research Technician is to aid the Research Associate, Research Scientists, and Senior Research Scientists with experiments and research. The Research Technician can be expected to perform protein purification using chromatography, write Standard Operating Procedures and Master Batch Records, and assist with assay development and optimization. The Research Technician will report to a Senior Research Scientist. | 8/30/2022 |
| 6174 | Tenaya Therapeutics South San Francisco, CA Molecular Biology RAII SRAI or SRAII Upstream Process Development BS/MS in a biological science Exp: RA II: 1-3 Years |
Seeking a Qualified Candidate for a RAII/SRAI/SRAII within the Process Development Team. You will design, assemble, propagate and characterize constructs to support development projects and pipeline operations. This role will also have the opportunity to lead development of novel constructs and characterization. An ideal candidate strives to complete project milestones within departmental/corporate timelines and strategically executes protocols to troubleshoot complex operations and assays as needed. | 8/30/2022 |
| 6175 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate , RNA Analytics - HPLC BS. / M.S. or equivalent in a relevant discipline Exp: 1 - 2 years |
Tessera is seeking a Research Associate (RA) to join the analytical team to characterize synthetic oligonucleotides and mRNA using HPLC. The position will require creativity, resourcefulness, and adaptability. We are searching for experienced, enthusiastic, innovative, and highly motivated individuals who are comfortable working in a fast-paced entrepreneurial environment. | 8/30/2022 |
| 6176 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, Cell Therapy Discovery BS/MS degree in biological sciences Exp: 1+ years |
We are looking for a Research Associate to join the Cell Therapy Discovery team to advance early-stage cell-based research with Tessera’s novel Gene Writing and Gene Rewriting technology for ex vivo and in vivo cell therapy applications. The Senior Research Associate will work closely with scientists in the Cell Therapy team to translate novel gene writing technologies to develop innovative therapeutics for Oncology disorders. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 8/30/2022 |
| 6177 | Tessera Therapeutics Somerville, MA Research Associate I/II, High-throughput mRNA Manufacturing (Contract) BS/MS degree in either Chemical Engineering, Bioengineering, or Biological Sciences. Exp: 1+ years |
Tessera Therapeutics is seeking a motivated and creative Research Associate I (or Research Associate II) to join a team of scientists and engineers focused on process development of mRNA. This is a contract position through the end of the year. This will include, but not limited to, high-throughput production process development and automation, mRNA manufacturing, process execution to make material for preclinical studies. This individual will join a dynamic, rapidly growing, and highly collaborative team that is driving RNA process development for a novel platform of Gene Writing. | 8/30/2022 |
| 6178 | Tri-Pac South Bend, IN Assistant Engineer Bachelor's Degree in Engineering or Science discipline Exp: 0-2 years |
The Assistant Engineer will demonstrate his/her knowledge of biologics manufacturing processes, including fermentation, purification, and bulk filling processes and work independently in a team environment, influencing team decisions, and exercising sound judgement in determining compliant and robust validation approaches. He/she will have the ability to multi-task with a demonstrated track record in meeting deliverable timelines and must demonstrate the ability to think critically and analytically with acumen for troubleshooting and problem solving and is a strong team player aligned with company corporate values. This individual will have good interpersonal, verbal, and written communication skills and can function effectively and independently in a fast-paced and dynamic environment. He/she is self-motivated and willing to tackle assignments and development opportunities outside of job scope as needed. Demonstrates hands on experience with facility/equipment/utility qualification, cleaning validation, process validation, and sterilization validation experience in GMP environment and with CIP/SIP cycle development. | 8/30/2022 |
| 6179 | Tri-Pac South Bend, IN Laboratory Technician Associates or Bachelor’s degree in a scientific field preferred Exp: 1-2 years’ |
The Lab Technician performs chemical analysis and testing on chemical raw materials and in-process/finished batches according to methods and specifications as defined by the customer. He/she assists with compiling, analyzing and interpretation of results as well as maintaining the flow of samples and paperwork through the laboratory. The Lab Technician maintains laboratory equipment and instrumentation to ensure ideal usage and has a strong attention to detail. The Lab Technician is able to effectively correspond with internal customers, has excellent organizational skills, able to perform physically demanding work such as moving and lifting equipment and capable of standing for long periods of time. | 8/30/2022 |
| 6180 | Tris-Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. | 9/1/2022 |
| 6181 | Tris-Pharma Monmouth Junction, NJ AR&D Scientist - ALL LEVELS Bachelors degree in Chemistry or related scientific field Exp: 1 year |
To support expectations of continued growth Tris is expanding the Laboratories at our Monmouth Junction, NJ facility and has openings for all levels of Analytical Research and Development (AR&D) Scientists. | 9/1/2022 |
| 6182 | TScan Therapeutics Waltham, MA Research Associate/Sr. Research Associate, Translational Research (RA30-1) BS/MS Exp: BS: 0-5+ years; MS: 0-2+ years |
TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a highly motivated researcher to join our Translational team as Research Associate/Senior Research Associate, supporting both pre-clinical and clinical-stage programs. The ideal candidate should have relevant experience in primary T cell culture, immunoassays, flow cytometry, and cancer biology, and enjoy exciting, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 9/1/2022 |
| 6183 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate, In Vivo Pharmacology (RA07-7) BS/MS Exp: For RA level: BS and 0-3+ years; For Sr. RA level: MS and 0-2+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a motivated researcher to join our In Vivo Pharmacology team as a Research Associate/Senior Research Associate, supporting the preclinical development of our lead therapeutic TCRs. The ideal candidate should have relevant experience in in vivo pharmacology, mechanism of action and anti-tumor efficacy studies, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 9/1/2022 |
| 6184 | TScan Therapeutics Waltham, MA Computational Research Associate/Senior Research Associate (RA02-8) Master’s degree Exp: 1+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a motivated bioinformatician/computational biologist to join our team as Computational Research Associate, supporting our novel target identification and validation workflow in house, with focus on Next Generation Sequencing and genomic data analyses. The ideal candidate should have relevant experience in genomics, computer science and bioinformatics, and enjoy fast-paced, collaborative and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 9/1/2022 |
| 6185 | Twist Bioscience South San Francisco, CA Research Associate B.S. or M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field Exp: 0-2 years |
This position is geared towards working with the DNA and RNA product lines. The candidate must be capable of maintaining current products, troubleshooting control fragment assembly issues, and analyzing data related to current and future controls. Up-and-coming scientists that demonstrate self-motivation and enthusiasm for scientific bench work are strongly encouraged. Your work will be mainly at the bench; however, you will have the opportunity to use high-throughput robotic instruments as well as coding and bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 9/1/2022 |
| 6186 | Twist Bioscience South San Francisco, CA Research Associate, Antibody Engineering BS Exp: 1-year |
We are seeking an outstanding, innovative, and creative Research associate to join our antibody discovery effort. This research associate will play multiple roles within the Biopharma group and will work within a team responsible for antibody discovery utilizing a number of in vitro display technologies, e.g. phage display, ribosome display, and yeast display. | 9/1/2022 |
| 6187 | Twist Bioscience South San Francisco, CA Research Associate, NGS Bachelors/ Associates degree in biology, chemistry, biochemistry Exp: 1-3 years |
Twist is seeking a highly motivated individual to help support customers and their Next Generation Sequencing needs. This individual will work closely with R&D and Customer Support teams to help develop custom solutions for various sequencing applications. The candidate will be detail oriented who is compatible with fast paced environments. | 9/1/2022 |
| 6188 | Twist Bioscience South San Francisco, CA Research Associate, NGS Viral Controls B.S. or M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field Exp: 0-2 years |
This position is geared towards working with the DNA and RNA controls product lines. The candidate must be capable of maintaining current products, troubleshooting control fragment assembly issues, and analyzing data related to current and future controls. Up-and-coming scientists that demonstrate self-motivation and enthusiasm for scientific bench work are strongly encouraged. Your work will be mainly at the bench; however, you will have the opportunity to use high-throughput robotic instruments as well as coding and bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 9/1/2022 |
| 6189 | Twist Bioscience South San Francisco, CA Research Associate, Process Development B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
We are looking for an outstanding Research Associate to join our Specialty Production Team in South San Francisco. The Research Associate will support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast-paced startup environment. The ideal candidate will work independently, be very organized, have excellent molecular biology knowledge and skills, and communicate effectively with peers/management. The Candidate must be comfortable working in a LEAN manufacturing/ controlled laboratory environment. | 9/1/2022 |
| 6190 | Twist Bioscience South San Francisco, CA Research Associate, Specialty Production B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
We are looking for an outstanding Research Associate to join our Specialty Production Team in South San Francisco. The Research Associate will support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast-paced startup environment. The ideal candidate will work independently, be very organized, have excellent molecular biology knowledge and skills, and communicate effectively with peers/management. The Candidate must be comfortable working in a LEAN manufacturing/ controlled laboratory environment. | 9/1/2022 |
| 6191 | Ultragenyx Pharmaceutical Woburn, MA Research Associate, Analytical Development - Gene Therapy BS in Biology, Biological Science, Genetics or a related discipline Exp: 0-2 years |
Working in close collaboration with other Analytical Development team members, the Research Associate will perform analytical testing for AAV gene therapy vectors and be involved in method development and optimization. This researcher will be highly involved in analysis of AAV therapeutic materials with molecular and genomic analytical methods to support process development, product characterizations, and QC release testing. We are looking for an individual with proven ability to work collaboratively with other researchers to finish projects within timelines and to work creatively under supervision. | 9/1/2022 |
| 6192 | Ultragenyx Pharmaceutical Cambridge, MA Contract Research Associate I, Non-Clinical (Temporary) B.S. or equivalent degree in biology, molecular biology, biochemistry, virology or related discipline Exp: 1 year |
The candidate will support advancement of innovative AAV-based therapeutics by using a variety of research methods including mammalian histology, molecular and biochemical techniques, as well as cell-based assays | 9/1/2022 |
| 6193 | Ultragenyx Pharmaceutical Cambridge, MA Research Associate, Vector Core - Gene Therapy BSc in Biology, Molecular Biology, Biochemistry, Virology or cognate discipline Exp: 1-2 years |
Reporting to the Senior Director of Vector Platform Research, the Research Associate will support and execute the production and purification of rAAV from HEK and HeLa Producer Cell Line systems, as well as iterative improvement of these processes by performing hypothesis-driven research. Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site and thus will be subject to certain on-site safety protocols during the pandemic. | 9/1/2022 |
| 6194 | Variantyx Framingham, MA NGS Laboratory Technician BSc, MSc in life sciences/Biology/Molecular Biology/Biochemistry or related field. Exp: 1 year |
The NGS Laboratory Technician performs high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. Including CAP/CLIA and NY State Requirements. The Laboratory Technician is an on-site position in Framingham, MA; Full time 2nd shift, 3rd shift or weekend shift. | 9/1/2022 |
| 6195 | Verve Therapeutics Cambridge, MA Research Associate/Sr. Research Associate, gRNA Technology M.S. or B.S. in biological sciences, chemistry, or biomedical/chemical engineering Exp: 0-4 years |
We are seeking a Research Associate to join a team focused on developing gRNA technology, including chemical modification, sequence design, and early-stage process development of gRNA for Verve’s novel CRISPR gene editing therapies. The ideal candidate will have interest in nucleic acid technology, biochemistry, and analytics, and a desire to apply creative problem-solving skills to develop RNA constructs and evaluate production processes. In this highly cross-functional role, you will perform a wide range of experiments to support projects across different functional areas throughout Verve R&D and Tech Ops. | 9/1/2022 |
| 6196 | Vesigen Therapeutics Cambridge, MA Research Associate I-II, Tissue Culture Core Master’s degree Exp: 1-3 years |
Vesigen is seeking a creative and highly motivated Research Associate to join our team and help advance the development of the company’s exciting ARMMs technology. The candidate will be an integral member of the R&D team, with opportunities to learn and contribute and develop numerous preclinical programs across several therapeutic areas. | 9/1/2022 |
| 6197 | Vir Biotechnology San Francisco, CA Research Associate II MA/MS Exp: 1 years |
Vir Biotechnology is seeking a motivated and collaborative Research Associate to help drive new efforts in the discovery and development of novel therapies for the treatment of infectious disease. You will work within a highly collaborative group environment with other passionate scientists. The successful candidate, under guidance, will participate in discovery and translational research efforts aimed at identifying and characterizing novel therapeutic targets, investigating mechanism of action of therapeutics and defining optimal drug combinations through evaluation in the appropriate in vitro models. | 9/1/2022 |
| 6198 | Voyager Therapeutics Cambridge, MA Research Associate II, In Vivo Biology B.S. or M.S. in Biology or related discipline Exp: 1 to 3 years |
We are seeking an experienced and highly motivated biologist to contribute to our biochemical and in vivo research team at our facility in Cambridge, Massachusetts. This is an ideal position for an individual with a background in vivo biology and biochemical methods, who thrives in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. The individual will work at the bench on multiple projects and be responsible for experimental execution and data analysis for research studies supporting therapeutic programs and platform discovery research. We are looking for prior hands-on experience with protein purification, ELISA, western blot, mouse handling, perfusion and tissue collection. | 9/1/2022 |
| 6199 | Voyager Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Assay Development Bachelor’s degree in Molecular/Cellular Biology, Biochemistry, Pharmacology or a similar field Exp: 1-5 years |
We are seeking an experienced and highly motivated Research Associate or Senior Research Associate to contribute to our Translational Research team at our facility in Cambridge, Massachusetts. This is an ideal position for an individual with a strong background in molecular and biochemical assays and methods development, who thrives in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. The successful candidate will participate in the development, implementation, and execution of assays to assess vector biodistribution, transgene expression, and pharmacodynamic effects in ex vivo tissues from preclinical gene therapy program studies and novel capsid discovery platform studies. | 9/1/2022 |
| 6200 | Promega San Luis Obispo, CA Manufacturing Associate B.S./BSE degree Exp: 1-3 years |
This position is responsible for performing a variety of basic operations, under direct supervision, to manufacture bioluminescent and fluorescent chemical products which are used as tools to study gene functions, enzymes, drug interactions, metabolism and more. This is an interesting and challenging role on a highly energetic and talented team. This position is full-time, 40 hours per week. | 8/22/2022 |
| 6201 | Protomer Technologies Indianapolis, IN Associate Oligonucleotide Chemist BS and/or MS in Chemistry, Biochemistry, or related field Exp: 1-2+ years |
In the RNA Therapeutics Team, both basic and applied sciences are vital. We are looking for creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. Key facets of the role are solid-phase synthesis of custom nucleic acid oligomers and conjugation of ligands for specific cellular and tissue delivery to progress an innovative preclinical portfolio. We are building state-of-the art expertise in major oligonucleotide-based modalities and delivery approaches, with an emphasis on innovative approaches with potential for breakthrough efficacy. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 8/23/2022 |
| 6202 | Protomer Technologies New York, NY Research Associate, Analytical Development BS and/or MS Exp: 1+ years |
The Analytical Development (AD) team is a group of energetic, brilliant, fun, and motivated individuals. We independently work on different AAV-based gene therapy programs while continuously working as a team to achieve our goals. We are a small but quickly growing family. This groupAD is responsible for developing robust and innovative analytical methods to support internal and external manufacturing processes. While much of the day-to-day operations required wet-lab work, our team focuses on not only building everyone’s technical expertise but also fostering an environment for career growth as scientists in the biopharmaceutical industry. The Research Associate will be responsible for the development and establishment of novel analytical methods for characterization of AAV-based products. | 8/23/2022 |
| 6203 | Protomer Technologies Indianapolis, IN Chemist - Oligonucleotide Synthesis BS and/or MS in Chemistry, Biochemistry, or related field Exp: 1-2+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to accelerate the core capabilities and development of internal RNAi-based clinical candidates. Do you have an aptitude for large scale oligonucleotide synthesis and have a desire to learn about RNAi modalities in discovery and development that focus on identifying impactful therapies for the patient? We want you on our team! | 8/23/2022 |
| 6204 | Protomer Technologies San Diego, CA Associate - Protein Mass Spectrometry Masters in chemistry, biochemistry or a similar field Exp: 0 years |
The Protein Biosciences group at the Lilly Biotechnology Center San Diego seeks a BS or MS level scientist with experience in protein mass spectrometry to join a team responsible for the expression, purification, and characterization of protein therapeutics. The primary focus of this position will be the characterization of proteins. | 8/24/2022 |
| 6205 | Protomer Technologies Branchburg Township, NJ Quality Control Lab Systems Analyst Bachelor’s Degree in a scientific field related to the lab (e.g., Chemistry, Microbiology or Biology) Exp: 1 year |
This position will provide in depth support to the QC laboratories for new and existing computerized laboratory systems and databases. Assist in the selection, implementation, maintenance, and continuous improvement of computerized systems within the QC laboratories. Serve as a technical lead on system implementation and validation projects and serve as a technical representative on project teams. Provides technical support in the diagnosis and resolution of QC computerized system issues. Identify compliance and data integrity issues related to QC computerized systems and implement effective resolutions. | 8/24/2022 |
| 6206 | PTC Therapeutics South Plainfield, NJ BS/MS Biologist ( Nucleotide Repeat Disorders) BS/MS Biologist ( Nucleotide Repeat Disorders) BS/MS Biologist ( Nucleotide Repeat Disorders) Master’s degree in a scientific discipline, preferably Biology or Biochemistry or Neuroscience Exp: 0- 2 years |
The BS/MS Biologist is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. | 8/24/2022 |
| 6207 | Purdue Pharma Wilson, NC Chemist BA or BS degree in Chemistry or closely related science. Exp: six months - two years |
The Quality Specialist I, Chemist is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing and GMP review in support of the analysis of raw materials, packaging components, ancillary solutions, in-process samples, finished product method development and/or transfers, cleaning/process validations, and stability samples. Will follow standard procedures in accordance with cGMP, GLP, DEA and company policies and procedures. | 8/24/2022 |
| 6208 | Purigen Biosystems Pleasanton, CA Research Associate - I/II B.S. in Molecular Biology, Biology, Biochemistry or similar life sciences discipline Exp: 1-3 years |
Purigen Biosystems, Inc., a Venture-backed, life science tools start-up company in the San Francisco bay area, is seeking an experienced Research Associate to join our Operations team. The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. This is a hands-on position for the highly qualified, self-motivated candidate who wants to enable cutting-edge life sciences technologies in a fast-paced, start-up environment. | 8/24/2022 |
| 6209 | Qiagen Germantown, MD Associate Scientist, Assay Development MS degree Exp: 1+ years |
Contribute to a team working on the design, development and improvement of immunodiagnostic assays based on ELISA and/or lateral flow technology. Coordinating with other team members to enable the planning and execution of studies accurately and timely. Execute feasibility and verification studies as required. Recording and analyzing experimental data and results, verifying data integrity and accuracy, and reporting on findings to the team. Maintaining accurate laboratory notebooks in a timely fashion and provides input to technical reports covering data Propose novel strategies and technologies and independently apply basic scientific principles to solve problems. Perform literature searches and have a broad knowledge and deep understanding of literature in Immunoassay and infectious disease fields. Review method development data, verification/validation reports, and bioanalytical reports. Thoroughly analyze results and methods, solve analytical problems, and troubleshoot assays. | 8/24/2022 |
| 6210 | Qiagen Beverly, MA Lab Technician I Bachelor’s degree from four year college or university Exp: 0-2 years |
The Lab Technician I performs assigned manufacturing support duties in a ISO 13485 environment. Job performance will involve a variety of activities including: - Ensure the cleanliness and availability of glassware and labware for production use. - Operate autoclave and ensure sterility of equipment and associated labware - Operate Lancer glasswasher and ensure the cleanliness of labware. - Ensure the Sanitization area is appropriately stocked. - Prepare buffers and solutions. - Communicate as a team member with other functional groups, via face to face, email and written reports. | 8/24/2022 |
| 6211 | Qiagen Beverly, MA Protein Purification Technician I Bachelor’s degree from four year college or university Exp: 1-2 years |
The Protein Purification Technician I performs assigned manufacturing and process development duties in a ISO 13485 environment. Job performance will involve a variety of activities including: - Execute development and production scale purification protocols as directed. - Work with standard scientific equipment as described in relevant procedures; AKTA Purifier and AKTA Pilot, UV spectrophotometer, balances, chromatography columns, SDS-PAGE, autoclaves, pH meter, refrigerators, freezers, biohazard safety cabinets. - Record results in laboratory notebooks; required to have meticulous organization and record keeping skills. - Prepare buffers and solutions. - Communicate as a team member with other functional groups, via face to face, email and written reports. Position Requirements | 8/24/2022 |
| 6212 | Qiagen Beverly, MA Protein Purification Technician II Bachelor’s degree from a four year college or university Exp: 1 – 3 years |
Responsibilities of the Protein Purification Technician II will primarily include activities directly related to the purification of proteins (enzymes and antibodies). Execute development and production scale protein purification procsses as specified. Perform standard operations as described in relevant procedures. This includes the following: Column chromatography via AKTA Purifier and Pilot system Upstream process separation techniques such as homogenization, cell lysis, and centrifugation Sample analysis via chromatogram, UV Spectroscopy and SDS PAGE Packing and evaluation of a variety of different columns Buffer and solution preparation Small scale bacterial fermentations Perform all activities in an ISO 13485 environment | 8/24/2022 |
| 6213 | Quidel San Diego, CA Development Associate II (Assay Development) MA/MS in life sciences Exp: 0-2 years’ |
Responsibilities include activities to support research and new product development. Perform self-directed experiments or as directed by Scientist or Manager · Resolve product performance issues · Summarize experimental data, draw conclusions and make recommendations · Conduct research, process development, validations, creation and implementation of documentation and training of personnel · Maintain project documentation and laboratory notebooks in accordance with internal Quidel and external regulatory requirements as part of the design control process · Maintain a safe working environment | 8/24/2022 |
| 6214 | QuVA Pharma Bloomsbury, NJ Chemist B.S. or M.S. degree in chemistry, biology or related field Exp: 0- 2 years |
The individual will be required to perform either validation studies for analytical methods, conduct stability analyses on drug product, or test of Raw Materials. This individual will execute testing per current test methods and follow all applicable SOPs and cGMP guidelines. This individual will conduct analytical testing of finished sterile products, and raw materials, following all written procedures and cGMP, and providing documentation of analyses. This individual will report any issues to the Supervisor upon discovery. This individual will work with the Supervisor to understand overall expectations and execute them independently based on the prioritization of projects. This individual will work with the Supervisor or Manager to understand overall expectations and provide data to meet project milestones. | 8/24/2022 |
| 6215 | QuVA Pharma Bloomsbury, NJ Microbiologist B.S. degree in related field (preferably Microbiology) Exp: 0-2 years |
Performs individual hands-on work in the sterility testing program. The Microbiologist provides scientific guidance and interpretation of environmental monitoring and microbiology results to production management. | 8/24/2022 |
| 6216 | Reaction Biology Malvern, PA QC Specialist – Biochemical Assays Master’s degree in a related field Exp: 1+ years |
We are currently seeking a QC Specialist for our Malvern, PA facility. We are looking for a reliable and motivated individual with a strong science background to work in our lab. The successful candidate will provide quality control review of laboratory records, reports, and other documentation for accuracy, appropriateness, and timeliness. | 8/24/2022 |
| 6217 | Reaction Biology Malvern, PA Research Associate I – Biochemical Assays Research Associate I – Biochemical Assays Bachelor’s Degree or equivalent in biochemistry or related discipline Exp: 0-3 years |
We are currently seeking a Research Associate I for our Malvern, PA facility. We are looking for a reliable and motivated individual with a strong science background to work in our lab. The position is a bench position with the primary duty of executing a variety of enzymatic assays. | 8/24/2022 |
| 6218 | Resursion Pharmaceuticals Salt Lake City, UT Research Associate, In Vitro Pharmacology Masters degree in cell biology or related field Exp: 1+ years |
You’ll join a team focused on developing and screening in vitro assays for the world’s leading company in AI-guided drug discovery. You will help develop the technology and build the assays used to discover potential therapeutics and determine how and where they interact with human biology. With treatments for hundreds of diseases in our sights, you will work on a diverse array of programs side-by-side with automation engineers, biologists, chemists, data scientists, software engineers, and many others. Together, we generate the data, systems, tools, and methods to accelerate the discovery of treatments for pathologies that affect the lives of countless individuals. | 8/24/2022 |
| 6219 | Minaris Regenerative Medicine Mountain View, CA QC Analytical Associate I BA/BS in a science or relevant field required Exp: 0-2 years |
The Quality Control Analytical Associate serves as a support role to clinical and commercial production. The QC Analytical Associate will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. | 8/24/2022 |
| 6220 | Minaris Regenerative Medicine Allendale, NJ QA Associate II BS or higher education degree in a scientifically related field Exp: 1 -3 years |
The Quality Assurance Associate II is responsible for performing Quality Assurance activities under direct supervision of daily tasks in support of Quality Systems and/or client procedures including but not limited to document management, review of QC data, material releases and final product releases as well as assisting Quality management with department needs. | 8/24/2022 |
| 6221 | SAMDI Tech Chicago, IL Research Assistant B.S. in biology, biochemistry, chemistry, or related field Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. | 8/25/2022 |
| 6222 | Sanofi Pasteur Chattanooga, TN Quality Control Lab Chemist I Bachelor’s degree in Chemistry or related field. Exp: Zero to three years |
Role Responsibilities Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. Secure and file the MSDS sheet for all laboratory chemicals and reagents. Maintain a log of laboratory chemicals and reagents. Assure that chemicals and reagents are within their respective expiration date or shelf life. Discard any expired or obsolete chemicals or reagents as appropriate. Oversee the proper disposal of laboratory waste in conformance to the established procedure. | 8/25/2022 |
| 6223 | Sanofi Pasteur Swiftwater, PA Quality Control Technician - Vaccine Bachelor Degree or Mater Degree in Microbiology or Biological Sciences Exp: 0-5 years’ |
KEY RESPONSIBILITIES: This position supports execution of routine testing in the Quality Control Microbiology laboratory while strictly adhering to site work instructions, Federal Regulations, cGMP, and Sanofi Pasteur policies and procedures. This position requires the individual to perform route testing as scheduled to support production, method validation as well as the stability program and completing required documentation. Knowledge of general Microbiological techniques including aseptic processing and culturing of both bacterial and viral isolates. Demonstrated knowledge and proficiency of functions within the following systems is required: SAP, Trackwise, LIMS, MASTER and eDoc. Activities include: Assist with maintaining safety and compliance of the laboratory work area; Perform cleaning of laboratories, equipment, and ancillary areas as required; Attend/Contribute to scheduled team meetings, department and safety meetings. This position requires proficiency and understanding of the theory related to processes, assays, and equipment as well as the ability to identify issues/trends. Participates in training activities including their individual professional development, creation/revision of training modules as well as provide training to others on processes, procedures, assays, and equipment with which they are proficient. Demonstrate proficiency in use and knowledge of change controls, CAPAs, and the QA deviation system. Perform initial deviation investigations through analyst interview. Develop a working knowledge of appropriate compendia and/or regulatory guidance. This position will be filled as off-shift which includes second shift or weekends. | 8/25/2022 |
| 6224 | Sanofi Pasteur Ridgefield, NJ Validation Specialist I Bachelor's degree in Engineering or Science discipline Exp: 1 years |
Summary of Responsibilities: Perform a variety of moderately complex to complex tasks with minimal supervision in accordance with current cGMP, company, and departmental standards in a given protocol. This may include calibrating test instrument, qualifying equipment, and validating simple processes. Perform hands on qualification / validation execution work, e.g. Autoclave sterilization, Steam-In-Place, Clean Validation, VHP Decontamination, Temperature Mapping and Environmental Smoke studies. Generate qualification / validation protocols and reports, from a set template, for repetitive systems or assist in protocol development of new equipment or system. This position is needed to work with minimal supervision or independently with direction, and the work will be reviewed for soundness of judgment and overall adequacy / accuracy. This position will also consistently require to make independent decision and to exercise independent judgment. In addition, the duties of this position require advanced knowledge in specialized field of learning, e.g. Moist Heat Sterilization, Isolator with VHP Decontamination, Stability Chamber / Temperature Control Unit, simple equipment and Laboratory Instrument, simple PLC control system…etc. This position will also contribute to the completion of milestones associated with specific projects or routine technical tasks. Failures to achieve results or erroneous decisions or recommendation may cause delay in program schedule and may results in the allocation of additional resources. The position will be the primarily internal company contacts or infrequent inter organizational / outside customer contacts. | 8/25/2022 |
| 6225 | Sanofi Pasteur Framingham, MA Quality Control Analyst I Bachelor’s Degree Exp: 0-2 Years |
Shift Schedule: Sunday-Wednesday shift, 12:00 pm - 10:30 pm Quality Control Microbiology (QCM) is responsible for testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations. Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation. Quality Control is also responsible for assisting in site wide studies and projects. | 8/25/2022 |
| 6226 | Sanofi Genzyme Lexington, MA mRNA, Research Associate, Pre-Clinical Plasmid Production M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology) Exp: 1-3 years |
As an experienced molecular biologist, you will be supporting the design, development and implementation of a robust plasmid growth, extraction, and purification process for preclinical supercoiled and linearized plasmid production. | 8/25/2022 |
| 6227 | Sanofi Genzyme Waltham, MA Research Associate, Genomic Medicine Unit CMC Cell Culture Process Development Bachelor’s degree in biological science or engineering discipline Exp: 0-1 years |
The cell culture process development group is responsible for viral vector production optimization and development of next generation production platforms to support high dose therapeutic products. The group is seeking a motivated Research Associate to join the team. | 8/25/2022 |
| 6228 | Sanofi Genzyme Framingham, MA Upstream Manufacturing Associate Upstream Manufacturing Associate Bachelor’s degree Exp: 1-3 years |
The Upstream Manufacturing Department performs small and large-scale cell culture operations, harvest filtration, and initial capture chromatography steps in a new manufacturing facility. The 24/7 large-scale therapeutic protein manufacturing facility uses single-use technology. The Upstream Department is responsible for all setup, operation, and breakdown of equipment associated with cell culture and capture column operations. This position is responsible for performing a variety of complex tasks under the general guidance and in accordance with the manufacturing instruction set and current GMPs. | 8/25/2022 |
| 6229 | Sarepta Therapeutics Columbus, OH Research Associate I/II, Gene Therapy R&D Research Associate I/II, Gene Therapy R&D B.A. or B.S. degree in biological sciences or related field Exp: 1-3 years |
Sarepta Therapeutics is seeking a motivated individual to provide laboratory support, perform experiments, collect and analyze data on in vitro and in vivo studies to investigate gene therapies for rare genetic diseases. Activities will include assessment of protein expression, tissue pathology, and disease phenotype in animal models of neuromuscular disorders. The RA participates in development, GCP/GLP qualification, and validation of biomarker assays to support preclinical development, clinical trials and clinical development decision-making. | 8/25/2022 |
| 6230 | Sarepta Therapeutics Andover, MA Associate I ELISA Associate I ELISA Bachelor’s degree in molecular or cell biology Exp: 0 - 2 years |
This individual will join a dynamic and vibrant team to support quality control laboratory activities for the development of AAV therapeutics conducted at Sarepta Andover facility. The individual will assist in conducting ELISA assays to support QC release and method validation. The individual may work under the direction of a subject matter expert conducting experiments and support analytical method validation and qualification activities. All aspects of this position involve working in a GMP compliant manner. | 8/25/2022 |
| 6231 | Sarepta Therapeutics Andover, MA Associate II - rcAAV B.S. or M.S. degree in molecular biology or cell biology Exp: QC Associate I/II: 0 – 2 years |
This individual will support quality control activities conducted at Sarepta Andover facility in the field of AAV therapeutic release and stability. The individual will perform Replication Competent Adeno-associated virus (rcAAV) Detection assay using Quantitative Polymerase Chain Reaction, qPCR as endpoint readout of release and stability samples for early/late phase clinical and commercial AAV therapeutic products. This individual may assist in troubleshooting rcAAV assays being conducted in Andover, MA and at contract testing laboratories. All aspects of this position involve working in a GMP compliant manner. The individual will lead a team engaged in conducting rcAAV assays in support of release and stability of commercial AAV therapeutic products. This individual will also be responsible for supervising and training 1-3 junior QC associates as well management of their performance. | 8/25/2022 |
| 6232 | Sarepta Therapeutics Andover, MA Gene Therapy Potency Associate B.S. degree in molecular biology or cell biology Exp: QC Associate I/II: 0 – 2 years |
This individual will support quality control laboratory activities conducted at Sarepta Andover facility in the field of AAV therapeutic release and stability. The individual will assist in conducting GMP QC release and stability testing using state of art In vitro Potency Assay. The candidate should have hands on experience of SDS-PAGE, Western blotting, enzyme activity measurements, protein extraction and quantification methods. The position requires a background in cell culture, tissue lysate sample preparation, protein analysis and performing assays in a BSL-2 environment. The individual will work under the direction of a subject matter expert conducting experiments and support analytical method validation and qualification activities. All aspects of this position involve working in a GMP compliant manner. | 8/25/2022 |
| 6233 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 8/25/2022 |
| 6234 | SDIX Newark, DE Biotechnician I BS/BA degree in biology, chemistry, or related field such as veterinarian studies Exp: 0 to 3 years |
Maintain laboratory in proper working order through organization and procurement of supplies, routine maintenance of laboratory equipment, organization and maintenance of reagents, and general laboratory hygiene. Verify and ensure that proper processes and procedures are followed in accordance with SOPs. Support manufacturing aspects of SDIX’s products by executing protocols, utilizing basic knowledge of biology, chemistry, laboratory equipment and computer software. | 8/25/2022 |
| 6235 | SDIX Windham, ME Biotechnician I BA/BS in biology, chemistry or related field such as veterinary studies. Exp: Up to 3 years |
This position supports manufacturing of SDIX’s products by executing protocols using basic knowledge of biology, chemistry, laboratory equipment and computer software. The Biotechnician I is responsible for conducting operations using various laboratory techniques, organizing and procuring supplies, and maintaining a clean and safe work environment. | 8/26/2022 |
| 6236 | Septodont Cambridge (Ontario Canada), CA Chemist I Bachelor's Degree in Chemistry or related discipline. Exp: One to two years |
The Chemist I is an entry-level position and is accountable to the Manager – Stability and Analytical Services. This person will be responsible for chemistry testing and review in the support of the Analytical testing and Tech Transfer for customer (CDMO) and R&D projects. | 8/26/2022 |
| 6237 | Sigmapharm Laboratories Bensalem, PA Associate Scientist AD BS in Chemistry or Pharmaceutical sciences Exp: 1-3 years |
Perform physical and chemical testing of raw material, packaging material, in-process, release, and stability samples. Record experimental data, analyze results, and maintain accurate and up-to-date notebooks. Support ANDA/NDA projects form development to approval with guidance. Support method development and method validation work. Assist in maintaining the laboratory in compliance with SOPs, CGMPs, FDA and OSHA. Use and maintain instruments, such as HPLC, GC, Dissolution, UV-VIS, IR, Titrator, etc. Troubleshoot and perform minor maintenance and repair of lab instrumentation. Support investigation and troubleshooting of analytical issues. | 8/26/2022 |
| 6238 | Smithers West Trenton, NJ Associate Research Scientist (Molecular and Cell Biology) MS in relevant field Exp: 1-2 years |
Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance. PDS works with customers to develop new methods, validate existing methods, and perform the assays necessary to analyze samples from patients on more than 100 clinical trials. PDS is seeking an Associate Research Scientist with experience in Molecular and Cell Biology to join our team. The successful candidate is able to apply prior experience and knowledge to successfully perform in a laboratory environment under regulated conditions. | 8/26/2022 |
| 6239 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field Exp: 6 months |
Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 8/26/2022 |
| 6240 | NuProbe Houston, TX Technician I/II BA/BS or higher in Biology, Bioinformatics, or a related field Exp: 0 – 3 years |
The Technician I/II executes Research & Development activities which is vital to the success of the company. This position utilizes wet lab skills for executing qPCR and NGS experiments. Experience with analyzing NGS data using terminal/open-source tools and/or writing scripts in at least one language (python, R, Perl, Matlab etc.) is preferred. | 8/15/2022 |
| 6241 | NuProbe Houston, TX Technician I (Innovation) BA/BS or higher in Biology, Biochemistry, Biotechnology, or a related field Exp: 0 – 3 years |
The Research Technician I – Innovation Department executes most of the research & development protocol activity which is vital to the success of the company. This position handles sensitive data and comes with a high degree of trust. | 8/15/2022 |
| 6242 | NuVasive San Diego, CA Test Engineer, Verification Advanced degree in Biomedical, Electrical or Mechanical Engineering, or related technical discipline Advanced degree in Biomedical, Electrical or Mech Exp: 0+ years |
NuVasive is seeking an Electrical, Mechanical, or Biomedical Engineer with test development experience for our Surgical Intelligence System Test Engineering Team. Our team is part of a larger development group that focuses on integrating technology into products and systems designed for spine surgical use in the operating room. As our Human Factors Engineer, you will be working with a team to produce medical devices that are safe and effective for use by integrating the user experience into the design and development process. Your responsibility is to advocate for intended users and patient safety by minimizing potential use errors. In addition, you will participate in Design Validation and Usability studies by contributing to test plan development, developing test protocols, and helping prepare technical documentation for test reports. This is a hands-on role; outside of planning and documentation generation, you will be supporting formative and summative usability testing with end users and cadaver validation labs – a confident, passionate, and easy-going personality is a must for this role to work with multiple cross-functional teams and to interface with end-users (i.e., surgeons). | 8/15/2022 |
| 6243 | Ocean Ridge Biosciences Exton, PA Associate Quality Control Specialist-Biomarker Bachelor Degree or Master Degree in Chemistry, Biochemistry or other scientific field Exp: 0-2 years |
Review of Biomarker bioanalytical data (notebook documentation, raw data, and LIMS data) for accuracy, consistency, and completeness to ensure compliance with SOPs and GLP. Review method development/qualification/validation reports and sample analysis reports including text and data for accuracy and consistency. Preparation of bioanalytical test result data tables for clinical testing reports. Review of client data transfer specifications. Prepare and transmit client data transfer tables. Review Data Transfer Specification Other duties as assigned.Review of Biomarker bioanalytical data (notebook documentation, raw data, and LIMS data) for accuracy, consistency, and completeness to ensure compliance with SOPs and GLP. | 8/15/2022 |
| 6244 | Ocean Ridge Biosciences Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 8/15/2022 |
| 6245 | Ocean Ridge Biosciences Hayward, CA Research Associate M.S. degree in related scientific discipline Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 8/15/2022 |
| 6246 | Ocean Ridge Biosciences Chicago, IL Analytical Chemist B.S. degree in chemistry Exp: 0-3 years |
Duties include methods transfer/development and validation, determination of analytes in dose formulations and accurate preparation of formulations (e.g., solutions, suspensions, etc.) to be used in toxicology studies. Knowledge of performing these duties with strict adherence to Good Laboratory Practice Regulations (FDA, EPA and OECD) is a plus. Other responsibilities as assigned. | 8/15/2022 |
| 6247 | Ocean Ridge Biosciences Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree Exp: 1-3 years |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 8/15/2022 |
| 6248 | Ocean Ridge Biosciences Hayward, CA Research Associate-Biologics MS / MA in biochemistry, biology, chemistry, pharmaceutics or related scientific discipline Exp: 0-2 years |
Conduct study design, lab-testing, data analysis and PI review. Author and/or review methods, protocols and other related documents. Assist PIs in maintaining project quality, meeting compliance requirements and timelines. Prepare notebooks, study binders, data packets, data summaries, methods, and qualification/validation protocols under the supervision of lab management / PIs Monitor reagent and consumable inventories and timely submit the orders for the support of both project and non-project based programs After receiving sufficient training, perform as PI and manage the overall planning, execution, and quality of assigned MD/MV and sample analysis projects under the supervision of lab management Participate TC and communicate with sponsors to solve technical issues and update projects, provide weekly summary to the sponsors | 8/15/2022 |
| 6249 | Ocular Therapeutix Bedford, MA Process Development Engineer I Bachelor’s degree in Chemistry, Biology, Biomedical or Chemical Engineering or related discipline. Exp: 0-2 years |
We are seeking an experienced engineer/scientist to execute drug product/process development project activities for hydrogel-based candidates. The role includes but is not limited to product design and evaluation, manufacturing process development, line layout and equipment procurement, and GMP manufacturing of clinical trial material. This individual will execute assigned project activities and work with project team members to develop and manufacture the drug products. They may oversee the execution of project tasks and monitor the activities and deliverables of project aspects in a leadership role. | 8/16/2022 |
| 6250 | Ology Bioservices East Norriton, PA Research Associate II, Process Development, Cell Therapy Bachelor’s or Master’s degree in immunology, cell biology, bioengineering or a related field. Exp: 1-3 years |
Resilience is seeking a talented Research Associate 2 to expand our cell therapy process development team. With the guidance of process development senior staff, this researcher will develop and optimize manufacturing processes for gene-modified cell products to advance Resilience’s biomanufacturing platforms and the clinical programs of Resilience’s partners. | 8/16/2022 |
| 6251 | Ology Bioservices Allston, MA Research Associate, Analytical Development Research Associate, Analytical Development Research Associate, Analytical Development Bachelor’s degree (B.S) or equivalent in Chemistry, Biochemistry or related field Exp: 0-2 years’ |
As a research associate in the nucleic acid franchise analytical development team the candidate will be responsible for executing analytical techniques in support of method development, qualification and routine testing support on client based and internal platform programs · Collaborate, assist, and design in method development of new assays and execution of lab procedures in support of nucleic acid process characterization and release methods for drug substance and drug product. · Methodologies include: molecular/PCR-based methods, nucleic acid sequencing, immunodetection, and fingerprinting approaches, aqueous and reversed phase chromatography, liquid-solid separation methods, and capillary and other gel electrophoresis methodologies. | 8/16/2022 |
| 6252 | Ology Bioservices Waltham, MA Research Associate II, Process Development, Stem Cells and Regenerative Medicine Bachelor’s or Master’s degree in cell Biology, immunology or a related discipline Exp: 1+ years |
Resilience is seeking a talented Research Associate II to join us as a valued member of the Cyto Innovation Process Development team. This researcher will focus on hands-on execution of protocols involving induced pluripotent stem cells (iPSCs) for Resilience’s developing Regenerative Medicine Modality. The successful candidate will support the development of Resilience’s best-in-class hypoimmune iPSC generation platform and will collaborate broadly with colleagues in platform R&D, analytical development, and other teams across the Resilience biomanufacturing network. | 8/16/2022 |
| 6253 | OpGen Rockville, MD Laboratory Technician BS degree Exp: 1+ years’ |
The Laboratory Technician will perform, implement, and improve laboratory workflows for NGS based detection of antimicrobial resistance. The Laboratory Technician will be responsible for delivering high quality lab results to our global partners, clinicians and microbiologists to derive actionable insights. | 8/16/2022 |
| 6254 | OpGen Rockville, MD Junior Scientist BS degree Exp: 1+ years’ |
The Junior Scientist will perform, implement, and improve laboratory workflows for NGS based detection of antimicrobial resistance. The Junior Scientist will be responsible for delivering high quality lab results to our global partners, clinicians and microbiologists to derive actionable insights. | 8/16/2022 |
| 6255 | OraSure New Brighton, MN Lab Technician I B.Sc. or M.S. degree in Biology, Biochemistry, Molecular Biology Exp: 1+ year |
Lab Technician I will be expected to work collaboratively as part of a team. In this role, the Lab Technician I will be responsible for managing timelines, performing hands-on lab work, maintaining processing records and working in compliance with our accreditations and quality standards. | 8/16/2022 |
| 6256 | Orna Therapeutics Cambridge, MA Research Associate/Senior Research Associate – RNA Production B.S. in biology, biochemistry or a related discipline required. Exp: one year |
We are seeking an exceptional researcher to join our team as a Research Associate/Sr. Research Associate to help build and maintain our proprietary RNA production process. The ideal candidate has at least a bachelor’s degree in a biological/biochemical related field with RNA handling and process development experience. They will be able to quickly learn, troubleshoot, and integrate new protocols into existing workflows; possess strong oral and written communication capabilities; demonstrate excellent collaboration & interpersonal skills; and be adept at problem solving in a fast-paced environment. | 8/16/2022 |
| 6257 | Pacira Biosciences San Diego, CA Microbiologist 1 BS degree in Microbiology or other life science Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products | 8/16/2022 |
| 6258 | Pall West Sacramento, CA Manufacturing Scientist -1 Bachelor’s degree or higher in a Science field Exp: 0-2 years’ |
The Manufacturing Scientist -1 for Beckman Coulter Diagnostics is responsible for the success and routine operations of a custom product, by supporting various elements of routine manufacturing, QC testing, equipment maintenance, troubleshooting, and inventory management of the product line. This position is part of the Technical Operations team located in West Sacramento, CA and will be on-site full-time. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. | 8/16/2022 |
| 6259 | Pall Cortland, NY Associate Scientist Bachelor’s degree Chemistry, Chemical Engineering, Materials Science Exp: 1-3 years |
The Associate Scientist or Engineer provides performance data to R&D, Marketing, Sales and Quality that enable their ability to serve our customers in the Microelectronics industry. They are part of a dynamic team that develops and standardizes new test methods that allows us to characterize our materials and products in ways that as closely as possible mimics their end-use. | 8/16/2022 |
| 6260 | Pall Madison, WI Associate Scientist I, Analytical Method Validation Bachelor’s degree in Microbiology, Biochemistry, Biotechnology, or related field Exp: 0-2 years |
The Associate Scientist I, Analytical Method Validation (AMV) in R&D is responsible for validating bioanalytical methods that are transferred either from clients or from the Analytical Method Development (AMD) group. This role will mostly focus on performing experiments to generate data to support validation of these methods. Duties include, but are not limited to, performing experiments, interpreting results, communicating results, and drafting documentation. The Associate Scientist I must interact closely with the AMD team to ensure that methods are transferred correctly. With guidance from the Senior Scientist, the Associate Scientist I executes validation protocols. The Associate Scientist I relies on education and experience to troubleshoot experiments, with technical oversight provided by the Senior Scientist, when necessary. The Associate Scientist I will also be qualified to train others on the methods they have validated. | 8/16/2022 |
| 6261 | Pall Westborough and Boston, MA Laboratory Operations Assistant Bachelor’s Degree Exp: one year |
The Accelerator Process Development group at Pall specializes in designing, optimizing, and transferring scalable processes from pre-clinical to validated cGMP ready manufacturing. The team is seeking a highly motivated Laboratory Operations Assistant to coordinate the day-to-day lab operations, ensuring that client projects are progressing, and systems are set-up and maintained according to quality standards and SOPs. This includes, but not limited to, ordering laboratory supplies, calibration of laboratory equipment, maintenance of inventory database, and supporting both scientists and project managers. | 8/16/2022 |
| 6262 | Fulgent Genetics Temple City, CA Lab Technician I Bachelor’s Degree in molecular biology, genetics, or related field. Exp: 1 to 4 years |
The Lab Technician I is responsible for performing clinical laboratory test procedures following standard operating (SOP) and quality assurance (QA) procedures under general supervision. The successful candidate will be a key contributor to a team committed to clinical sequencing and diagnostic test services. | 8/17/2022 |
| 6263 | Personalis Menlo Park, CA Clinical Lab Assistant 1 Bachelor of Science in Biotechnology or related field Exp: 0-1 years |
We are looking for a Clinical Lab Assistant to join our operations team who enjoys troubleshooting and problem solving in a dynamic, team-oriented environment. In this role, you will have the opportunity to participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. *Please note, this is a temp to hire opportunity with a typical duration of 3 months working as a temporary worker prior to conversion to employee status. Shift available: Tues to Sat PM (1-9:30 PM) – Training schedule may be different | 8/17/2022 |
| 6264 | Personalis Menlo Park, CA Clinical Lab Associate 1, Extractions BA/BS in a biological discipline Exp: 0-2 years |
This is a 3 month temp to hire position. We have openings for Sun-Thurs (AM or PM).As a team member of our small and growing biotech company, you’ll be integral to our shared mission of enabling precision medicine for cancer treatment. In support of our Clinical Lab Ops, your primary responsibilities will be performing DNA & RNA extractions, related QC, data analysis and other tasks in support of the next generation sequencing services. | 8/17/2022 |
| 6265 | Personalis Menlo Park, CA Clinical Lab Associate 1, Sequencing BA/BS in a biological discipline. Exp: 0-2 years |
As a team member of our small and growing biotech company, you’ll be integral to our shared mission of enabling precision medicine for cancer treatment. In support of our Clinical Lab Ops, your primary responsibilities will be performing next generation sequencing, related QC, data analysis and other tasks in support of the next generation sequencing services. | 8/17/2022 |
| 6266 | Personalis Menlo Park, CA Clinical Lab Associate I BA/BS in a biological discipline. Exp: 0-2+ years |
This is a 3 months temp to hire position. We have Multiple openings on the below teams for swing and day shifts (Tues - Sat or Sun - Thurs). You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. | 8/17/2022 |
| 6267 | Personalis Menlo Park, CA Clinical Lab Associate I, WGS BA/BS in a biological discipline Exp: 0-2 years |
This is a 3 months temp to hire position. We have openings for Swing (Sun - Thurs). Located in Menlo Park, CA, we are seeking a talented and highly motivated Clinical Laboratory Associate to join our Operations Team. Under the direction of the Laboratory Manager, the successful candidate will help grow the Whole Genome and cell free DNA (cfDNA) Operations Sequencing Services Team. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. Primary responsibilities will be performing and assisting in laboratory tests, processes and analyses according to the laboratory’s standard operating procedures. Candidates for this position should be highly motivated, a team player, and able to thrive in a high-throughput operations environment. | 8/17/2022 |
| 6268 | Pharmaron Germantown, MD Laboratory Technician, Sample Management Bachelor’s degree in related field Exp: 6 months to 1 year |
e are looking for motivated individuals to join our laboratory in Germantown, MD. This is an opportunity for recent graduates to make a real impact in a highly scientific and regulated environment, demonstrate leadership, ambition and the desire to grow with the department. | 8/17/2022 |
| 6269 | Pharmaceutics International Hunt Valley, MD QA Associate Bachelor’s degree in Microbiology or Chemistry. Bachelor’s degree in Microbiology or Chemistry. Exp: one (1) to three (3) years |
Witness and verify the QA functions related to manufacturing of sterile product while adhering to the cGMP ICH and USP/EP/Health Canada guidelines as written -- to ensure that the day-to-day tasks of the Quality Assurance Unit supports the overall business plan while maintaining the highest quality products and ensuring the safety, identity, strength, purity, and quality that the drug is purported to possess. Perform “Line Clearance” and “Cleaning Verification” for manufacturing and packaging operations per established Standard Operating Procedures (SOPs) and Batch/Packaging and Labeling Records’ requirements. Perform in-process sampling, inspections, testing, and batch record reviews during manufacturing and packaging operations as per established SOPs and Batch/Packaging and Labeling Records’ requirements. Perform Acceptable Quality Level (AQL) sampling for in-process and finished product. | 8/17/2022 |
| 6270 | Phitonex Carlsbad, CA Scientist I, Cell Biology Bachelor's degree preferred or equivalent certification/experience in a life science field is required. Exp: 0-2 years |
As part of the Cell Biology R&D team, the Scientist will develop new products that empower our customers to discover and gain a deeper understanding of how cells work and enable research in cell biology, immunology, oncology, and infectious disease. If you can picture yourself in a dynamic and empowering environment where your contributions will have a direct impact on life science research and where you will have the opportunity to learn and develop your career, we encourage you to apply to join our team! | 8/17/2022 |
| 6271 | Phitonex Rockford, IL Production Scientist 1, Biochemistry Bachelor of Science degree in a Biochemistry, Chemistry, Biological Sciences, or other Life Science emphasis. Exp: Entry-Level |
As a new hire in this role you are eligible for a $1,000 Sign-On Bonus! The Production Scientist I, Biochemistry is an introductory manufacturing laboratory position. All work is conducted with an emphasis on safety and within the guidelines and requirements of ISO-regulated/lean manufacturing environment. This position requires working efficiently and effectively to achieve goals relative to safety, quality, delivery, and cost. The Production Scientist I, Biochemistry position will work under the guidance of more senior personnel. | 8/17/2022 |
| 6272 | Phitonex Frederick, MD Scientist I, Cell Biology R&D Bachelor’s degree in Biology, Bioengineering, Biochemistry, or a related subject area Exp: 1-3 years |
You will work as a part of Advanced Cell Models R&D to support ongoing projects within the Thermo Fisher product commercialization process under the Gibco™ brand. You must have experience with cell culture, either immortalized cell lines or primary cells. The candidate should also have familiarity with downstream analyses, including the evaluation of cells via microscopy, Western blot, flow cytometry, or similar techniques. An innovative and curious mentality, attention to detail, and ability to multitask while maintaining a focus on critical projects are essential. | 8/17/2022 |
| 6273 | Phitonex Florence, SC Scientist I - Process R&D BS/BA degree in chemistry or BS in science Exp: 0-3 years |
This is an entry-level opportunity to support the Process R&D efforts at the Florence, SC facility. You will join a team of synthetic organic chemists to support manufacturing of pharmaceutical ingredients at the Florence, SC east site. Many of our products are already in the market serving patients. We work on a variety of projects for existing and new clients with a good combination of routine and challenging work. At this position, you will perform hands-on experimentation and learn skills to run reactions, analyze samples and interpret results. We have a dynamic and fast-paced working environment while keeping a good work-and-life balance. We encourage employees to participate technical discussions and expand their skill sets. | 8/17/2022 |
| 6274 | Phitonex Greenville, NC QC Scientist I (Environmental Monitoring): 12-hour Nights Bachelor’s degree in related discipline preferred, associate degree in a science related field, preferably Biology, minimally required. Exp: Up to 2 years |
Provides routine analyses in a microbiology environment by following standard practices. Follows standard operation procedures as assigned for monitoring in classified environments. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results. Documenting, reporting and analyzing data in a laboratory setting. Typical shift hours are 6p-6a on a 2-2-3 rotating schedule. | 8/17/2022 |
| 6275 | Phitonex San Diego, CA Scientist I, Chemistry Bachelor of Science or Bachelor of Arts degree, preferably in Biology or Chemistry or equivalent, is required. Exp: 1+ year |
Manufacture in a lab setting following standard operating procedures (SOP). Will apply basic laboratory techniques, calculations, materials measurement, operation of laboratory equipment and record keeping vital to manufacture products in a GMP environment. Wet chemistry formulation, dispense, and lyophilization. Responsible for Batch Data Records, notebooks (if required) and work order documents. Maintain equipment, product inventories and related records as assigned. | 8/18/2022 |
| 6276 | Plex Pharma San Diego, CA Research Associate, Biology & Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field Exp: 1-3 years |
The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 8/18/2022 |
| 6277 | Principia Biopharma Framingham, MA Laboratory Technician, Cell Culture Development Associate’s degree Exp: 1 year |
Join a team dedicated to supporting cell culture process development and other activities within Upstream Mammalian Platform CMC organization located in Framingham, MA. We are looking for an individual that is familiar with sterile technique, cell culture lab equipment and has good laboratory and documentation practices. | 8/18/2022 |
| 6278 | Principia Biopharma Framingham, MA Senior Research Associate, Cell Therapy Flow Cytometry Master’s degree in Biology/Biochemistry or related discipline Exp: 1 – 3 years |
The Senior Research Associate is responsible for executing test methods under control of established procedures. Specifically, performing in-process and release testing of cellular therapies out of our 45 NYA manufacturing facility. Additional functions will include interpretation of data, preparation of test documentation, and management of analytical databases. We are looking for a candidate that is capable of learning quickly with the goal of executing analytical methods and managing assigned test schedules, with excellent communication skills. | 8/18/2022 |
| 6279 | Principia Biopharma Cambridge, MA Associate Scientist, Nanoparticle Development BS in Chemical Engineering, Biomedical Engineering, Chemistry, Material Science, or closely related field Exp: 1+ years |
This position provides a unique opportunity to partake in nanoparticle formulation, process development, and characterization activities with a focus on process scale-up. Additionally, working with an inter-disciplinary team of chemists, biologists and engineers provides an understanding of the drug discovery, pre-clinical research and development paradigm. As such, we are interested in candidates with diverse backgrounds and interests. As part of a nimble, fast-growing team, the individual will have the opportunity to make significant contributions to the company’s mission on a daily basis. | 8/18/2022 |
| 6280 | Khloris Biosciences Mountain View, CA Cell Therapy Manufacturing Technician B.S. degree in biology, biochemistry, bioengineering, or related technical field Exp: 0-5 years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated cell therapy manufacturing technician to join our team. The selected candidate will work closely with lead manufacturing technicians, scientists, participate in project and team meeting, and work in a multidisciplinary environment. The duties of this position will involve supporting a multidisciplinary manufacturing team in developing Khloris cell therapy platforms. The ideal candidate will have hands-on expertise and comprehensive understanding of cell therapy manufacturing processes. | 8/8/2022 |
| 6281 | Lantheus Medical Imaging N. Billerica, MA Manufacturing Technician 4 - 2nd Shift Bachelor Degree in a science related field Exp: 1 – 2 years |
The objective of this position is to perform manufacturing operations required to produce pharmaceutical products in a timely manner compliant with cGMP, OSHA, and other regulatory requirements. Under the direction and on-the-floor guidance of the 2nd Shift Manufacturing Supervisor, the Manufacturing Technician IV will become qualified and independently capable of performing all aspects of internal cold manufacturing operations. Such operations include, but are not limited to, receipt and transfer of materials and components into the manufacturing unit operation, component and equipment cleaning and preparation, operation of automated manufacturing equipment with good aseptic technique, completion of production transactions within the ERP system, completion of paper-based production records and forms in accordance with GDP. | 8/9/2022 |
| 6282 | Lonza Houston, TX Research Associate, Bioassay Services Bachelor’s Degree or Master’s Degree in Biological Sciences Exp: entry level years |
Research Associate, Bioassay Services, performs analytical support, assay development and optimization, and assay qualification. This position is also responsible for writing Method SOPs and Forms. Responsible for writing protocols and reports for Assay Qualification and Assay Validation. Oversees training of QC Analysts on new assays and transferring these assays to QC. Interacts with clients in meetings specifically about Assay Tech Transfer, Qualification and Validation | 8/9/2022 |
| 6283 | Lonza Houston, TX Research Associate Bachelor’s Degree or Master’s Degree in Biological Sciences Exp: entry level years |
Research Associate will support our Process Development and Bioassay Services group. This individual will provide technical support to Scientists and other Research Associates including conducting scientific experiments as well as the tools to conduct and collect data. This individual will also support the Lab Manager and perform common laboratory duties including supply of material, equipment maintenance, and general lab duties. | 8/9/2022 |
| 6284 | Lonza Tampa, FL Lab Technician Bachelor’s Degree in Science Exp: 1 year |
Lonza Tampa is hiring a Lab Technician for our R&D laboratory. The incumbent will carries out the practical work in the laboratory like equipment cleaning, change overs, process execution, or physical testing of materials. Takes over responsibility for lab organization and upkeep with minimal assistance. Uses judgement based on practice and precedence. | 8/9/2022 |
| 6285 | Lonza Houston, TX Lab Assistant Bachelor’s degree in Life Science, Biotechnology, or Bioengineering Exp: 1 year |
Lonza is seeking a highly motivated research associate to support analytical activities, assay development and optimization in the Viral Vector Research and Development team (R&D). This role in entry level and we will train individual to execute assays for characterizing viral vectors and support in assay development activities while supporting team in the lab current projects, while completing daily lab maintenance. | 8/9/2022 |
| 6286 | Lonza Houston, TX Research Associate, Bioassay Services Bachelor’s Degree or Master’s Degree in Biological Sciences Exp: entry level years |
Research Associate, Bioassay Services, performs analytical support, assay development and optimization, and assay qualification. This position is also responsible for writing Method SOPs and Forms. Responsible for writing protocols and reports for Assay Qualification and Assay Validation. Oversees training of QC Analysts on new assays and transferring these assays to QC. Interacts with clients in meetings specifically about Assay Tech Transfer, Qualification and Validation | 8/9/2022 |
| 6287 | Loop Genomics San Jose, CA Service Research Associate B.Sc or M.ScB.Sc or M.ScB.Sc or M.Sc Exp: 1-2 years |
We are looking for an outstanding team player to join our NGS sample prep team and report to the Director of Molecular Biology. The individual will provide next generation sequencing service to our customers that incorporates Loop Genomics's long read technology with Illumina's short read sequencing platforms. This includes applying the standard operating procedure during NGS library preparation, as well as custom solutions tailored to the specific sequencing projects. The individual will also assist in testing and improving the robustness of Loop Genomics’s library preparation kits. This role requires excellent laboratory liquid handling skills and consistent performance of various wet lab operations. The ideal candidate is a dedicated and detail-oriented individual who thrives in a fast-paced work environment, has a solid background in molecular biology techniques, and shares our passion in bringing technology to change the current paradigm of DNA sequencing. | 8/9/2022 |
| 6288 | Loxo Oncology Louisville, CO Research Associate/Associate Scientist, Biophysics BS or MS Exp: 0-3+ years |
Loxo@Lilly's newly formed Drug Discovery group in Louisville, Colorado has an immediate opening for a researcher in Biophysics. The Loxo Drug Discovery group’s mission is to invent life-changing targeted therapies for cancer patient populations that are poorly treated by existing therapies. To that end, we are building a multi-disciplinary team of dedicated drug discovery scientists who are passionate about driving the science forward to create highly selective drugs for known oncogenic drivers. The ideal candidate is self-motivated, responsible, and a productive scientist who enjoys collaborating with biologists, chemists, and assay scientists. In this role, he/she will utilize a variety of assay technologies including mass spectrometry, fluorescence spectroscopy, surface plasmon resonance, and isothermal titration calorimetry to evaluate protein/ligand interactions. Experience in protein purification and characterization is a plus. This position requires excellent people skills, a positive can-do attitude, passion for lab work, attention to detail, and the ability to thrive in a highly interactive, fast-paced, team environment. | 8/9/2022 |
| 6289 | Lubrizol Life Science Health Bethlehelm, PA Associate Scientist Bachelor of Science in a related discipline Exp: 0 – 3 years |
Operating under the general guidance of the Director of DEDD, the Associate Scientist leads formulation efforts in the development of drug eluting devices withing the Bethlehem facility. The Associate Scientist has responsibility for executing product development, from inception to manufacturing of internal and client-based products. | 8/9/2022 |
| 6290 | Lubrizol Life Science Health Midland, MI Chemist B.A. or B.S. in Chemistry preferred Exp: 0-5 years |
The Lab Technician is responsible for all facets of testing, from sample preparation to reporting of results. The majority of the workday is spent in a laboratory setting working with new and used oils, solvents, chemicals and equipment utilized to complete testing. This person is responsible for ensuring safety and good housekeeping practices during daily operations, as well as, operating and maintaining the equipment. | 8/9/2022 |
| 6291 | Lung Biotechnology Manchester, NH Associate Process Engineer, Biomaterials Associate Process Engineer, Biomaterials Associate Process Engineer, Biomaterials Bachelor’s Degree in Arts/Sciences (BA/BS) in materials science, chemistry, chemical, mechanical or biomedical engineering (or equivalent) Exp: 1+ years |
The Associate Process Engineer, Biomaterials (OMG) will be responsible for scaling up and experimenting with large batches of ink to support process and product feasibility goals. This position will also be responsible for periodic quality control (QC) testing. | 8/10/2022 |
| 6292 | Lung Biotechnology RTP, NC Research Associate I/II - Bioscaffolds Research Associate I/II - Bioscaffolds Research Associate I/II - Bioscaffolds Bachelor’s degree in arts/sciences (BA/BS) in life science, engineering, biomedical science Exp: RA I: 1+ years |
Conduct and assist in product development and research efforts for tissue-based regenerative medicine products for treatment of pulmonary hypertension and other lung diseases. More specifically, support decellularization process development and focus on material and functional characterization of lung scaffold and RegenLung construct. | 8/10/2022 |
| 6293 | Lung Biotechnology Manchester, NH Associate Biomedical Engineer / Biomedical Engineer Associate Biomedical Engineer / Biomedical Engineer Associate Biomedical Engineer / Biomedical Eng Bachelor’s Degree in Arts/Sciences (BA/BS) in biomedical, chemical engineering, mechanical engineering, bioengineering or similar/related discipline Exp: 1+ years |
The Biomedical Engineer - Lung Function (OMG) will work on the preclincal team and will support and lead the functional evaluation of 3D printed scaffolds (both cellularized and un-cellularized) and will standardize methods for assessment of performance. This position will work closely with both the cellularization and print process teams of OMG. | 8/10/2022 |
| 6294 | Merieux NutriSciences Gainesville, FL Microbiologist 1 Bachelors preferred Exp: One (1)- 2 years |
The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 8/12/2022 |
| 6295 | Meso Scale Discovery Gaithersburg, MD Bioanalytical Associate I Bachelor’s degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, or other related area is req Exp: 1+ years |
The Bioanalytical Associate I is responsible for handling biological samples, reagents, and materials in support of sample testing and assay service projects. This is a laboratory based position whose primary function will be sample management and handling, under direct supervision and direction. The incumbent may also perform protein-based immunoassays on a routine basis with relatively high throughput (2-8 plates per day). The incumbent is expected to adhere to all standard operating procedures and policies established for execution of Bioanalytical studies and sample testing projects under applicable regulatory compliance requirements. | 8/12/2022 |
| 6296 | Moderna Therapeutics Cambridge, MA Research Associate, Nucleic Acid Technology BS or MS in Molecular Biology, Biochemistry, Biology, Chemical Engineering, or closely related field Exp: 1-5 years |
Moderna is seeking a curious, detail-oriented research associate for our Nucleic Acid Technology team. In this laboratory-based position, the individual will participate in the synthesis and analysis of research scale material using novel processes in support of Moderna’s mRNA platform. Implementation of novel processes will require the individual to experiment and optimize to establish new protocols. Laboratory experience with nucleic acids and detailed recordkeeping is essential for this role. Experience with HPLC and mass spectrometry is a plus. The candidate should have a background in biology, chemistry, or chemical engineering. The candidate should enjoy working in a dynamic and innovative environment and be flexible in working both individually and within cross-functional teams to enable cutting-edge nucleic acid research. | 8/12/2022 |
| 6297 | Moderna Therapeutics Norwood, MA Research Associate, Clinical Biomarker Laboratory, Virus Neutralization Assays & Bio-Analytics Bachelor or MSc in vaccine, virology, or related field. Exp: Fresh graduates are encouraged to apply |
Moderna is seeking an agile and motivated Research Associate to join the Clinical Immuno-Assay group to serve as analyst for the virus neutralization assay development, qualification/ validation, and sample analysis to support programs across multiple therapeutic areas. The candidate will need to perform analytical work and maintain clinical testing continuity. The ability to effectively communicate within a project team is expected. Preferably, the candidate has some prior experience in running assay validation and conducting data acquisition on clinical specimen. The candidate should be a collaborative team member and an excellent communicator to support Moderna’s portfolio needs. The individual will work closely with project team members to develop analytical methods and characterization tools in support of our clinical phase studies. The position will report to the group lead of Virus Neutralization Assay. | 8/12/2022 |
| 6298 | Moderna Therapeutics Norwood, MA Research Associate, Analytical Technical Operations BS in Analytical Biochemistry, Chemistry, Organic Chemistry, Chemical Engineering, or a related field Exp: 0-2 years |
We seek a motivated individual with experience in analytical chemistry to support Technical Development. Candidates should have experience with various analytical techniques such as LC, molecular biology, and biophysical characterization. In this laboratory-based position, the individual will oversee operation and troubleshooting of analytical equipment, including LC’s, plate readers and liquid handlers. Experience with lab automation is a plus. The candidate must thrive in a fast pace environment, have a collaborative spirit, and be curious and willing to learn new techniques to push process development forward. | 8/12/2022 |
| 6299 | Moderna Therapeutics Norwood, MA Engineer I, Process Development BS/MS in Chemical Engineering, Chemistry, Biochemical Engineering, Biochemistry or closely related field Exp: 0-3 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. We are seeking a Bioprocess scientist or engineer to reside in Moderna’s Technical Development organization in Norwood, MA. Our team’s goal is to envision, pilot, scale, characterize, transfer, and validate robust commercial GMP manufacturing processes. We seek applicants who are proactive, enthusiastic, and show a passion for process development. The successful candidate must be able to work in a fast paced and highly dynamic environment, will have relevant academic and or industrial experience in large molecule bioprocessing (e.g. reactions, mixing, chromatography, tangential flow and/or normal filtration), and will be able to contribute to both process development and commercialization related activities. This role requires close working relationships with Analytical, Manufacturing, Supply Chain, Quality, Regulatory and Program Management functions. | 8/12/2022 |
| 6300 | MP Biomedicals Solon, OH Production Chemist Bachelor of Science in Chemistry, Biochemistry, or Biology Exp: 0-3 years |
The production chemist will be trained in two different product lines: Immunology and Molecular Biology Liquids and will learn and be responsible for a wide variety of product formulation tasks. Such as, following and optimizing production processes while following safety protocols to produce quality research products in a timely fashion to meet customer demand. | 8/12/2022 |
| 6301 | MP Biomedicals Irvine, CA R&D Scientist I Bachelor’s or Master's degree Exp: 0-3 years |
The R&D Scientist I will support the R&D department through Cell Biology associated product development. We are seeking a highly motivated, creative R&D Scientist I with experience in life sciences cell, molecular, and immunology laboratories. This candidate will be expected to lead some projects independently and to work with other scientists in a highly collaborative team environment. Projects may include, but are not limited to, cellular functional assays, cell engineering, protein characterization, sample preparation through homogenizer, DNA and RNA extraction, preparation, and analysis (NGS). | 8/12/0202 |
| 6302 | DPT Laboratories Morgantown, WV Chemist II Bachelor's degree (or equivalent) Exp: 0-2 years |
Key responsibilities for this role include: Perform pharmaceutical testing including, but not limited to, HPLC, GC, TLC, UV, dissolution, and IR spectroscopy. Develop and validate analytical test methods for pharmaceutical products. Critically evaluate and audit data. Write technical analytical reports and procedures. | 8/12/2022 |
| 6303 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in Biology, Biochemistry or other relevant discipline Exp: 0-2 years |
We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. The ideal candidate should have good organizational skills, possess good problem solving, communication and interpersonal skills and to adapt rapidly to new challenges. | 8/12/2022 |
| 6304 | Natera San Carlos, CA Research Associate B.S. degree in molecular biology, related field, or equivalent. Exp: 1 year |
The Research Associate 1 performs research and/or development tasks in collaboration with others. Makes detailed observations, analyzes data, and interprets results. Investigates, creates and develops new methods and technologies for project advancement. Maintains high level of professional expertise through familiarity with scientific literature. | 8/12/2022 |
| 6305 | Nautilus Biotechnology San Carlos, CA Research Associate II Bachelor’s degree in a Life Science field Exp: 1 year |
We are hiring for a Research Associate II to join our growing team. The R&D probe characterization Research Associate II will support the research staff in characterizing affinity reagents using DNA and protein assays. The role will require the candidate to perform affinity measurements, assess data quality and understand why discrepancies may exist between affinity measurement techniques. As the candidate gains understanding of the differences between the assays, they will help nominate which candidate molecules to move forward in the pipeline, providing an opportunity for the candidate’s growth and development into new areas of the organization. | 8/12/2022 |
| 6306 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Weekend Shift (Fri.-Sun. - 7:00am to 7:00pm & Mon. - 8:00am to 12:00pm) BS or MS in Chemistry, Biochemistry or a related field required Exp: 0-3 years |
Position Summary: Support quality control testing and research and development activities as needed; Assists with additional work duties or responsibilities as evident or required; Performs other duties as assigned or apparent; Relies on instructions and pre-established guidelines to perform job functions; Works under immediate supervision. | 8/12/2022 |
| 6307 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Second Shift (Sun. - Thurs. - 2:00pm to 11:00pm) BS or MS in Chemistry, Biochemistry or a related field required Exp: 0-3 years |
Position Summary: Support quality control testing and research and development activities as needed; Assists with additional work duties or responsibilities as evident or required; Performs other duties as assigned or apparent; Relies on instructions and pre-established guidelines to perform job functions; Works under immediate supervision. | 8/12/2022 |
| 6308 | Nephron Pharmaceuticals West Columbia, SC Microbiology R&D Analyst I Master’s Degree in Microbiology or other science-related field Exp: 1 - 3 years |
Performs research and develops projects for both established and new products, including, but not limited to, microbiological test method validation/transfer/verification, procedures, investigations, and other non-specified projects or initiatives. Plans, organizes, and manages resources on method validation projects to assure technical quality and schedule adherence. Performs other duties as assigned or apparent. Works with different microbiological techniques and equipment, including but not limited to gram stain, turbidimetric endotoxin testing, liquid particle counter, isolator, bioburden, filtration analysis, sterility testing, aseptic process simulation, and MALDI-TOF. Performs different microbiological tests for R&D Microbiology and QC Microbiology, as needed; also understands and performs routine investigations related to Environmental Monitoring and laboratory testing. | 8/12/2022 |
| 6309 | NGM Biopharmaceuticals South San Francisco, CA Research Associate II / Sr. Research Associate, Antibody Engineering Bachelor/Master's degree in biochemistry, chemistry, or related field Exp: 0-2 years |
We are seeking a highly motivated Research Associate II/Sr. Research Associate to join our Antibody Engineering and Discovery group and contribute to the early drug discovery efforts. The successful candidate will play a critical role in characterization of antibody hits and identification of lead therapeutic candidates using various biophysical platforms | 8/12/2022 |
| 6310 | North Star Medical Technologies Beloit, WI Process Chemist Bachelor’s degree in Chemistry, Chemical Engineering or related physical science/engineering Exp: up to 2 years |
The Process Chemist is responsible for developing and scaling up chemical processes and recommending equipment for the commercial production of NorthStar products. They will work in laboratories and production facilities to develop and test chemical production processes. Processes will include having to work with radioactive materials. Testing may include the development of test methods and working with analytical instruments as required. | 8/12/2022 |
| 6311 | Novartis Carlsbad, CA Clinical Lab Associate Bachelor's degree in technology science or health-related field Exp: Entry-level |
Entry-level laboratory position providing support to clinical testing activities. Responsibilities may include initial intake and registration of patient specimens; handling and pre-analytical processing of patient specimens; data entry and quality check of patient information and pre-analytical data entered into the laboratory information system; slide preparation; and sample management/storage. | 8/12/2022 |
| 6312 | Novartis Cambridge, MA BS/MS Research Scientist, Oncology Drug Discovery - Biotherapeutics MS with basic knowledge in immuno-oncology, immunology or cell and molecular biology Exp: 0-4 years |
We are seeking a highly passionate and motivated research scientist to join our team at Novartis Oncology Biotherapeutics in Cambridge, MA. This position is ideal for someone who is creative, highly collaborative, result-oriented and wishes to combine their curiosity about oncology, cancer immunology and drug discovery to save patients’ lives. In this role, you will have the opportunities to contribute to exploratory and innovative biotherapeutic drug discovery for cancer using a variety of different assays to independently support research in this area. The successful candidate will become a crucial part of a dynamic and multidisciplinary group to interact with other functional groups and to understand the process of preclinical drug discovery, that will eventually transform the lives of cancer patients. | 8/12/2022 |
| 6313 | Norvartis Carlsbad, CA Laboratory Assistant (Digital Pathology Solutions) BS/BA with scientific emphasis preferred Exp: no experience required |
As a Laboratory Assistant at Navigate, you will perform and assist with laboratory operations under GCP/GLP/CLIA regulations to support clinical trial sample testing. | 8/12/2022 |
| 6314 | Novartis Cambridge, MA Synthetic Chemistry Research Scientist (BS or MS) BS or MS degree in synthetic organic chemistry Exp: 0 to 5+ years |
We would like to welcome a highly motivated, scientifically curious, and innovative synthetic chemist to our Synthesis Technologies Team within Global Discovery Chemistry (Cambridge, MA). You will join an energizing and collaborative research environment working alongside colleagues who are committed to improving human health through the discovery of transformative medicines. | 8/12/2022 |
| 6315 | Novavax Gaithersburg, MD Research Associate I (Contract to Hire) Bachelor’s degree in biological science, molecular biology, immunology Exp: RA II: 1-3 years |
We are seeking Research Associate II to join our Clinical Immunology department in Gaithersburg, MD. This role is a contract to hire position. This individual will play an important role in clinical testing activities related clinical samples including assay development and qualification. In addition, individual will be expected to generate accurate high throughput clinical data following qualified assays using high throughput clinical testing. | 8/12/2022 |
| 6316 | Novavax Gaithersburg, MD Lab Technician, Upstream Process Development (Contractor) – NanoFlu BS in chemical engineering, biochemistry, molecular biology, microbiology or related area Exp: 0-2 years' |
Collaborate and coordinate with colleagues in buffer preparation, broth clarification, and upstream material hand-off to downstream process development for additional purification steps Performs washing and decontamination of glassware and distributing to appropriate locations within the laboratories. Maintains glass washing facility, including picking up and cleaning of glassware May sterilize glassware and other items using an autoclave or depyrogenation oven Maintains laboratory equipment, inventory levels, and organization of laboratory supplies Maintains record keeping for duties performed Assist in shipping and receiving of supplies Performs other related duties as required Setup, monitor, and harvest bioreactor runs up to the 20L scale to support upstream and downstream process development efforts | 8/12/2022 |
| 6317 | NovoBiotic Pharmaceuticals Cambridge, MA Associate Scientist - Microbiologist B.S. or M.S. in Biology/Microbiology Exp: 0 to 5 years |
We are currently seeking to hire microbiologists with 0 to 5 years of experience. The successful applicant will perform microbiology lab work and data analysis to discover previously unculturable microorganisms from soil and marine environments and their identification by molecular taxonomy methods. Additional tasks will include detection of antibiotic production from these organisms and in vitro characterization of their properties, such as spectrum of activity, mechanism of action, resistance development and cytotoxicity | 8/12/2022 |
| 6318 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 8/12/2022 |
| 6319 | Nucelis San Diego, CA Senior Research Associate/Research Specialist, Strain Development MS degree Exp: 0-5 years |
We are looking for a highly motivated individual who will be part of the Strain Development team to create a robust high throughput strain engineering and testing platform in oleaginous yeast. You will work with molecular biologists, fermentation scientists, process engineers and analytical chemists to create and identify microbial strains with the highest potential to produce sustainable microbial products. | 8/12/2022 |
| 6320 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro - * 1500 sign on bonus * BS/BA Degree in Microbiology or Biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management | 8/1/2022 |
| 6321 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro - * 1500 sign on bonus * BS/BA Degree in Microbiology or Biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management | 8/1/2022 |
| 6322 | Hikma Columbus, OH Scientist I, QC Microbiology 1st Shift - 1946 B. S. in scientific field required Exp: One to three years |
To ensure that all products, raw materials and the environment for production are microbiologically acceptable while ensuring regulatory compliance standards and release times are met. | 8/1/2022 |
| 6323 | Hillrom Marion, NC Quality Engineer 1 B.S. in technical area (mechanical, electrical, chemical, biological, etc.) Exp: 0 - 2 year |
Ability to perform standalone repeat and/or routine validations with little or no guidance. Ability to provide requirements for change control based on procedural requirements Be able to assist, present, defend and communicate with external auditors and others validations or projects in which you lead or participated. Assist or lead process improvement projects (scrap reduction, defect reduction, etc.) with little or no guidance. Can work with other support groups (production, quality, laboratory, etc.) in a collaborative manner. Display a solid technical understanding of engineering principles and procedures (e.g. CAD and its application or scheduling a series of technical tasks utilizing software-based tools and/or specialties such and chemical, industrial or biological). Assists in the preparation and participation in technical reviews and responsible for organizing data and preparing appropriate documentation for assigned projects. Provide assistance to management or other engineers during design, installation, qualification and/or process monitoring. Provide technical reports and/or data driven analysis after training.Ability to perform standalone repeat and/or routine validations with little or no guidance. | 8/1/2022 |
| 6324 | Hillrom Round Lake, IL Quality Lab Associate I Bachelors degree in Chemistry or Science related degree Exp: 6 months or more |
The Quality Lab Associate I will be located at the Drug Delivery Chemistry Laboratories, Round Lake, IL. The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. This is a first shift position but will be required to work on weekends to support training of analysts and to support projects and/or production, as required. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 8/1/2022 |
| 6325 | i2O Therapeutics Boston, MA Wet Lab Associate BS in biochemistry, chemistry, chemical engineering or a related science field Exp: 1 year |
The Associate will primarily assist in and conduct, as appropriate, synthesis and analysis of compounds, preparation of samples for analysis, assays of chemical and biological samples, preparation of samples for shipping, and general upkeep of the lab and supplies. Primary responsibilities include supporting scientists in setting up, monitoring and analyzing samples from a variety of studies including drug solubility, stability and permeability. Other activities include ordering and receiving supplies, preparing ionic liquids and conducting standard assays on the synthesized ILs. They will also be trained in performing ELISA or other assays and HPLC or LCMS sample preparation and operation. The technician will assist in new investigative projects as needed for platform development. The position will work under modest supervision and in compliance with Lab Central regulations and company SOPs and guidance. | 8/2/2022 |
| 6326 | IDEAYA Biosciences South San Francisco, CA Research Associate, ex vivo Pharmacology BA/BS or MS (Research Associate) Exp: 1+ years’ |
IDEAYA is seeking a South San Francisco based Senior Research Associate for our Pharmacology and Toxicology group. This individual will play a key role in the development and execution of preclinical models to understand the efficacy and PK/PD relationships of our small molecule agents under development for the treatment of cancer. The ideal candidate will enjoy working with multi-disciplinary teams in a fast-paced environment and will have the passion to contribute to the discovery and development of novel therapeutic agents for cancer patients. | 8/2/2022 |
| 6327 | IDEAYA Biosciences South San Francisco, CA Research Associate/Senior Research Associate, Translational Sciences BS or MS degree in cell/molecular biology or Oncology Exp: 1 year |
We are seeking a highly-motivated, well-organized and laboratory-focused Research or Senior Research Associate (RA/SRA) that will play a key role in supporting project needs for Translational Research in an oncology small molecule development team. The successful candidate will work in a multidisciplinary team and contribute to the generation of novel therapeutics for the treatment of cancer. Position level will commensurate with experience. | 8/2/2022 |
| 6328 | Illumina San Diego, CA Research Associate - Material Science Research Associate - Material Science Research Associate - Material Science BS or MS degree in Chemistry (Physical Chemistry, Material Science, Analytical Chemistry). Exp: 0+ years |
We are seeking a motivated individual for a Research Associate position in the Research and Technology Development group based at our San Diego headquarters. As part of the Materials and Applied Surface Science group, you will play an integral role in developing new sequencing and array technologies and related applications. You will be part of multidisciplinary teams solving complex problems and investigating new research areas. With the rapidly evolving nature of our research work, the candidate should be able to adapt to a wide range of techniques and methods used in life sciences. | 8/2/2022 |
| 6329 | Illumina San Diego, CA Research Associate 1 - Material Science Research Associate 1 - Material Science Research Associate 1 - Material Science BS or MS degree in Chemistry (Physical Chemistry, Material Science, Analytical Chemistry). Exp: 0+ years |
As part of the Materials and Applied Surface Science group, you will play an integral role in developing new sequencing and array technologies and related applications. As the company moves fast, so does the technology we use, and the candidate will have to be adaptable to a wide range of techniques and methods used in life-sciences. | 8/2/2022 |
| 6330 | Illumina San Diego, CA Integration Research Associate 2 Integration Research Associate 2 Integration Research Associate 2 B.S./M.S. in Bioengineering, Chemical Engineering, Biochemistry, Analytical Chemistry, Biology, or equivalent B.S./M.S. in Bioengineering, Chemical En Exp: 0 - 2 years |
The Integration Research Associate 2 will work in a dynamic, team-oriented environment and help create genomic analysis tools used in the leading edge of research. This position will participate in the development of high quality, robust products through the integration of hardware, software, and chemistry components. They will execute test plans in order to optimize product performance. | 8/2/2022 |
| 6331 | Illumina San Diego, CA Research Associate, Assay Development Research Associate, Assay Development Research Associate, Assay Development Bachelor’s or Master's degree in biochemistry, molecular biology, genetics, genomics or related field. Exp: 0 - 5 years’ |
As a Research Associate within Illumina’s Assay Development team, you will work as part of multi-disciplinary Research & Development group to support sample preparation in the generation of sequencing based assays for clinical oncology applications. In this role you will primarily be responsible for preparing and testing samples to support assay development and optimization. | 8/2/2022 |
| 6332 | IMMY Norman, OK Antigen Technician I Bachelor’s degree in Microbiology, Biology, Biochemistry, or a related field Exp: 0-1 years |
The role of the Antigen Technician I is to produce high quality fungal and bacterial antigens to manufacture IMMY diagnostics. This technician will succeed in this role by gaining knowledge and understanding the history, processes, and goals of the BSL3 laboratory and cultures, including optimizing antigen reactivity, and increasing a more robust raw material inventory. This person must have high attention to detail, good aseptic technique, and lab skills. Under moderate supervision, they will perform various tasks such as media preparation, various fungal and bacterial species cultivation, harvesting and filtration of antigens, and post-quantitative and qualitive testing while keeping accurate and complete records using our ERP system. The Antigen Technician I may assist in various process validations and is encouraged to generate ideas to improve processes or product quality. | 8/2/2022 |
| 6333 | IMMY Norman, OK Antibody Technician I Bachelor’s degree in Microbiology, Biology, Biochemistry, or a related field Exp: 0-1 years |
The role of the Antibody Technician I is to produce high quality monoclonal and polyclonal antibodies to manufacture IMMY diagnostics. This technician will succeed in this role by gaining knowledge and understanding the history, processes, and goals of the Cell Culture Lab, including optimizing goat serum reactivity, and increasing a more robust antibody inventory. This person must have high attention to detail, good aseptic technique, and lab skills. Under moderate supervision, they will perform various tasks such as media preparation, hybridoma cultivation, harvesting and purification monoclonal antibodies, polyclonal goat antibody maintenance, and post-quantitative and qualitive testing while keeping accurate and complete records using our ERP system. The Antibody Technician I may assist in various process validations and is encouraged to generate ideas to improve processes or product quality. | 8/2/2022 |
| 6334 | Inova Diagnostics San Diego, CA Research Associate I Bachelor’s degree; Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: 1-2 years |
This position assists in developing current and future Inova Diagnostic product lines by performing laboratory activities to assist in developing new assays and/or identifying potential new biomarkers. This position works under the supervision of the R&D management team. It performs lab activities of limited scope, following good laboratory documentation practices and in accordance with Standard Operating Procedures and other Research and Quality System requirements. | 8/2/2022 |
| 6335 | Inova Diagnostics San Diego, CA Chemist I- Bioflash Manufacturing Bachelor's degree B.A. or B.S. or equivalent in the biological or related sciences Exp: 1-2 years |
Participates in the preparation of autoimmune diagnostic products, utilizing the Bioflash technology platform, following established procedures. Major duties include Bioflash bead and reagent preparation activities and the preparation of controls and conjugates for the Bioflash product lines. | 8/2/2022 |
| 6336 | Inova Diagnostics San Diego, CA Research Associate I Bachelor’s degree; Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: 1-2 years |
This position assists in developing current and future Inova Diagnostic product lines by performing laboratory activities to assist in developing new assays and/or identifying potential new biomarkers. This position works under the supervision of the R&D management team. It performs lab activities of limited scope, following good laboratory documentation practices and in accordance with Standard Operating Procedures and other Research and Quality System requirements. | 8/2/2022 |
| 6337 | Inova Diagnostics San Diego, CA Research Associate I Bachelor’s degree; Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: 1-2 years |
This position assists in developing current and future Inova Diagnostic product lines by performing laboratory activities to assist in developing new assays and/or identifying potential new biomarkers. This position works under the supervision of the R&D management team. It performs lab activities of limited scope, following good laboratory documentation practices and in accordance with Standard Operating Procedures and other Research and Quality System requirements. | 8/2/2022 |
| 6338 | Integral Molecular Philadelphia, PA Research Associate – Job ID# 05052022 (Fulltime with weekend coverage) bachelor’s degree in biology, bioengineering, or a related field is required Exp: 1–2 years |
To support our growth, we seek a Research Associate I, who will work with a dedicated group of scientists on the production and characterization of antibody therapeutics. This position will involve training Monday through Friday for approximately three months, and then will transition to a position (approximately 9am to 5pm) that will require you to work at least one weekend day (Tue-Sat or Thurs-Mon). | 8/2/2022 |
| 6339 | Integral Molecular Philadelphia, PA Research Associate (Job ID# 090306) bachelor’s degree in biology, bioengineering, or a related field is required Exp: 1–2 years |
To support our growth, we seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. | 8/2/2022 |
| 6340 | Integral Molecular Philadelphia, PA Research Technician (Job ID# 062319) Associate or Bachelor’s degree in Biology, Chemistry, medical technology or related field Exp: 6 months – 2 years |
To support our growth, we seek a Research Technician to join our Membrane Proteome Array research team. | 8/2/2022 |
| 6341 | Intellia Therapeutics Cambridge, MA Senior Research Associate Genomic Innovation and Screening MS in Molecular Biology, Biotechnology, or related field Exp: 0-2 or more years |
As a Senior Research Associate in the Genomic Innovation and Screening team, you will be primarily responsible for planning and executing cell-based screening assays to characterize and quantify gene editing events under the guidance of a scientist. If you are a strong, independent problem-solver, detail-oriented with a strong technical background in mammalian cell cultures, and enjoy working in cross-functional teams, this is the role for you. | 8/2/2022 |
| 6342 | Invitae San Francisco, CA DNA Extraction Laboratory Trainer Bachelor’s degree in clinical laboratory studies or equivalent science related studies Exp: 1+ years |
We're looking for a passionate individual that enjoys developing training and competency programs, instructing and guiding others with varying levels of experience, and driving quality and continuous improvement. As a part of our Technical Team and in partnership with the Extraction Operations Lead, you will ensure successful expansion and execution of our lab processes through the facilitation of training, competency and validation programs, coaching team members to be tomorrow’s technical leaders, and challenging yourself to delve into opportunities for professional development. This role requires on-site work at our San Francisco location as well as opportunity to work overtime and off-schedule days as needed to accommodate training schedules. | 8/2/2022 |
| 6343 | Invitae San Francisco, CA DNA Extraction Technician Bachelor’s degree in clinical laboratory studies or equivalent science related studies Exp: 1+ years |
SCHEDULE: Thur-Mon, 7:00 am - 3:30 pm Thur-Mon, 3:00 pm-11:30 pm We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work at our San Francisco location as well as ability to work overtime and off-schedule days as needed. | 8/2/2022 |
| 6344 | Invitae San Francisco, CA Engineering Technician Bachelor degree in an engineering or science field preferred Exp: 1 – 2 years |
SCHEDULE: Sun - Thurs (Hrs TBD but possible differential pay!) We are looking for a passionate and driven Engineering Technician to join our Equipment Engineering Team who can come in and own the day to day equipment tasks which maintain regulatory compliance, equipment states and a high functioning lab environment. This individual will be able to seamlessly interface with production and engineering teams to drive forward task completion. | 8/2/2022 |
| 6345 | Invitae San Francisco, CA Engineering Technician Bachelor degree in an engineering or science field preferred Exp: 1 – 2 years |
SCHEDULE: Sun - Thurs 10:30am - 7:00pm + differential pay! We are looking for a passionate and driven Engineering Technician to join our Equipment Engineering Team who can come in and own the day to day equipment tasks which maintain regulatory compliance, equipment states and a high functioning lab environment. This individual will be able to seamlessly interface with production and engineering teams to drive forward task completion. | 8/2/2022 |
| 6346 | Invitae Iselin, NJ Extraction Technician Bachelor’s or Master's degree in Medical Technology, Biology, Chemistry, Biochemistry or related life science Exp: 1 years |
SCHEDULE: Monday - Friday, 8:30 AM - 4:30 PM EST hours Our Iselin (Metropark), NJ operations team is looking for a passionate and focused Extraction Laboratory Technician I to join invitae and support high-complexity laboratory testing on patient specimens across various assays and platforms. The extraction team member will partner with the Extractions Lead to continuously improve daily extraction operations at our Metropark Laboratory. | 8/2/2022 |
| 6347 | Invitae San Francisco, CA Reagent Manufacturing Technician Bachelor's degree in Biochemistry, Chemistry, or a related science discipline Exp: 1+ years |
Multiple Openings! Schedule: Tues – Sat 3:00 pm-11:30 pm OR Sun - Thurs 3:00 pm-11:30 pm We're looking for a passionate Reagent Manufacturing Technician to join our Clinical Laboratory Operations team in San Francisco. You will work with complex laboratory testing (next-generation DNA sequencing) on patient specimens including all steps from specimen processing to data analysis, performing quality control and quality assurance procedures, and complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. | 8/3/2022 |
| 6348 | Iovance Biotherapeutics Philadelphia, PA Aseptic Manufacturing Technician (4 x10 hour work week) Minimum B.S. degree in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience. Exp: 0-5 years |
As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations is required. | 8/3/2022 |
| 6349 | Cambridge Isotope Laboratories Andover, MA Chemist I MS in Chemistry Exp: 0-3 years |
Cambridge Isotope Laboratories, Inc. (CIL) is seeking a Chemist I to join our production team based onsite in our Andover, MA location. As the leading company in a niche scientific market, CIL works with cutting edge researchers in clinical diagnostics, metabolic research, proteomics, environmental testing, protein discovery, drug development, metabolomics, and industrial research. CIL's growing customer base spans academia, pharmaceutical and industry, enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. Under the supervision of a group leader or supervisor, the Chemist I will work alongside an experienced scientist executing syntheses of isotopically labeled (13C, 15N, 18O and D isotopes) targets utilizing highly detailed SOPs and procedures. | 8/3/2022 |
| 6350 | Cambridge Isotope Laboratories Tewksbury, MA QA Associate I BA/BS within a Science or Quality concentration preferred Exp: 0-2 years |
The Quality Assurance Associate I is responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components in a GMP/ISO Environment. | 8/3/2022 |
| 6351 | Janssen Pharmaceuticals Cambridge, MA Associate Scientist M.S. Exp: 1-2 years |
We are seeking an Associate Scientist to join the TS team within the Immunology therapeutic area. This candidate will assist in designing and conducting biomarker assay strategies for the advancement of clinical development programs across the Immunology portfolio, with a focus on inflammatory and autoimmune diseases. The successful candidate will possess strong organization and communication skills and demonstrate the ability to design, shape, implement novel experiments and interpretation of data. | 8/3/2022 |
| 6352 | Janssen Pharmaceuticals San Diego, CA Associate Scientist I Master's Degree in Pharmacology, Neuroscience, or Biology Exp: 1 to 3 years |
We are seeking a highly motivated Associate Scientist with in-vitro neuropharmacology experience to join our Neuroimmunology Discovery research team in La Jolla, CA. The candidate will be passionate about the discovery and development of novel therapeutics for CNS disorders. Experimental work will be the core job function and as such the ideal candidate will spend close to full time at the bench generating data. It is critical that the successful candidate enjoys bench science, is scientifically curious, is self-motivated, and can demonstrate a high level of operational efficiency. Strong interpersonal skills, the ability to interact well with peers and collaborators, and strong written and oral communication skills are vital to success in this role. | 8/4/2022 |
| 6353 | Janssen Pharmaceuticals San Diego, CA Associate Scientist I, Neuroimmunology Master's Degree in Pharmacology, Neuroscience, or Biology Exp: 1 to 3 years |
We are seeking a highly motivated Associate Scientist with in-vivo neuropharmacology experience to join our Neuroimmunology Discovery research team. The candidate should be passionate about the discovery and development of novel therapeutics for CNS disorders. Experimental work will be the core job function and as such the ideal candidate will spend close to full time at the bench generating data. It is critical that the successful candidate enjoys bench science, is scientifically curious, is self-motivated, but also a strong standout colleague, and can demonstrate a high level of efficiency. Strong interpersonal skills, the ability to interact well with peers and collaborators, and strong written and oral communication skills are vital to success in this role. To be successful in the position, the candidate must be organized, and practice good laboratory principles including detailed notebook entry of experiments. | 8/4/2022 |
| 6354 | Janssen Pharmaceuticals Malvern, PA Associate Scientist, Biotherapeutics Drug Product Development (1 of 2) BS in Chemical, Bioengineering or related field Exp: 0-2 years |
The Associate Scientist in Drug Product Development (DPD) will work independently and in conjunction with appropriate teams to support program/project needs. The candidate will also help design and perform process development and engineering studies in support of DP fill-finish activities for biotherapeutics (e.g. mAbs, fusion proteins, multispecifics, etc). | 8/4/2022 |
| 6355 | Janssen Pharmaceuticals Malvern, PA Associate Scientist, Large Molecule Drug Product Development M.S. degree in Engineering (Biomedical, Bioengineering, Chemical, Electrical or Mechanical) Exp: 1 year |
The Associate Scientist in Large Molecule (LM) Drug Product Development (DPD) will work independently and in conjunction with development teams to support program/project needs. The candidate will also independently be accountable to lead, design, perform, and analyze studies in the development and engineering space in support of process and fill-finish activities for large molecules (e.g. monoclonal antibodies, fusion proteins, bi-specifics, gene therapies, cell therapies etc). | 8/4/2022 |
| 6356 | Janssen Pharmaceuticals Spring House, PA Associate Scientist II, Immunology Discovery Master’s degree in Immunology/Cell Biology or equivalent Exp: 1 year |
Janssen Research & Development, L.L.C., a Johnson & Johnson Company, is hiring a full-time Associate Scientist II position in the Immunology – Discovery group and will be located in Spring House, PA. | 8/4/2022 |
| 6357 | JRF Global Audubon, PA Scientist I/ Entry Level Chemist Bachelor of Science or advanced degree from an accredited college or university in chemistry or other science-related field Exp: 1-3 years |
Set up experiments under the guidance of a Scientist II and/or Team Lead Operate equipment, observe and log the progress of experiments Promptly submit experimental data / findings to the supervisor Promptly inform the supervisor of any problems encountered during the experiments. Assist in data entry in various formats and verify accuracy of data entry Assist in writing drafts of Protocols and Reports Provide a daily update on the progress, findings and results for each experiment. Compile the data as directed by the supervisor Check the quality and accuracy of the data before submission to the supervisor | 8/4/2022 |
| 6358 | KBI Biopharma Louisville, CO Research Associate I/II B.S. degree Exp: 0-2 years |
Open position available in the biophysical characterization core of the rapid analytics testing group. Responsible for analytical testing of client samples. Testing may include using client-based methods or some method development. Ideal candidate is able to quickly and accurately generate results. Technical writing skills are a plus. | 8/4/2022 |
| 6359 | KBI Biopharma Durham, NC Research Associate II B.S. in a related field Exp: 1-4 years |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 8/4/2022 |
| 6360 | Enzo Life Sciences Farmingdale, NY Associate Scientist BA/BS in Chemistry or related field Exp: 1+ years |
This position will be assisting the Manufacturing Team specifically with chemistry products and the in process testing required for regular small molecules. | 7/25/2022 |
| 6361 | Eurofins Viracor BioPharma Services Cambridge, MA Research Associate (In - Vivo) Bachelors degree or Associates Degree Exp: 1-2 years |
Under general supervision, performs a wide range of assigned research experiments with efficiency, accuracy and attention to detail. Performs in-life experiments including injections by conventional routes (IV, SC, IP, PO, IM) necropsy and tissue collection, blood sampling (submandibular and cardiac puncture) and general health evaluations. Comply with IACUC and AALAS guidelines on the care of use of experimental animals in research. Analyze biological samples using a variety of techniques, including ELISA activity assays and other kit based assays. Maintain meticulous records of experimental data and observations in laboratory notebooks in strict accordance with corporate guidelines.Under general supervision, performs a wide range of assigned research experiments with efficiency, accuracy and attention to detail. | 7/25/2022 |
| 6362 | Eurofins Viracor BioPharma Services San Diego, CA Research Associate I Research Associate I Research Associate I Bachelor’s degree in life sciences or related discipline Exp: 1+ years |
Become your most extraordinary self! Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. Join Eurofins Beacon Discovery part of the Eurofins Discovery ™ group of companies serving global clients in the Pharma and Biotech industries. Work alongside industry experts and collaborate with team members to directly and positively impact human health worldwide! We have a philosophy to support work life balance, career progression opportunities and offer many benefits such as formal mentoring programs, tuition reimbursement, extensive career training programs, competitive health benefits, paid time off and 10 annual paid holidays*. Become your most extraordinary self! Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. | 7/25/2022 |
| 6363 | Eurofins Viracor BioPharma Services South San Francisco, CA Research Associate, Molecular Biology Bachelor's degree in a science related discipline Exp: 0 to 3 years |
This is a technical position within a Gene Therapy group in South San Francisco to perform viral vector production in support of novel discovery programs. This job will involve assisting in all stages of Adeno-associated virus (AAV) production and purification. Key responsibilities will be establishing and maintaining relevant protocols, cell culture expansion and maintenance, transfections, sample filtration and purification, and data recording and entry. The candidate will be able to contribute to new technology development and concept generation. The ideal candidate will have a background in production and/or purification of proteins or other biomolecules (especially viral vectors) and some experience in an industry setting (especially CRO work). | 7/25/2022 |
| 6364 | Eurofins Viracor BioPharma Services Cambridge, MA Research Associate Candidate must have a degree in Cell and Molecular Biology, Biochemistry, Pharmaceutical, or other biological/analytical discipline Exp: 0-2 years |
Supports viral vector process development by providing analytical testing on DNA, ELISA, cell based platform within agreed upon turn-around; Demonstrate good understanding of ongoing programs and data generated in relation to the program; Troubleshoots issues as needed with supervision; Monitors assay performance to ensure GLP compliance | 7/25/2022 |
| 6365 | Eurofins Viracor BioPharma Services Fremont, CA Research Associate - Molecular Biology Bachelor’s degree Exp: 1-3 years |
Become your most extraordinary self! Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. Join Eurofins DiscoverX Products, LLC part of the Eurofins Discovery ™ group of companies serving global clients in the Pharma and Biotech industries. Work alongside industry experts and collaborate with team members to directly and positively impact human health worldwide! | 7/25/2022 |
| 6366 | Eurofins Viracor BioPharma Services Cambridge, MA Research Associate, Analytical Development Bachelor’s Degree in related science Exp: 0-2+ years |
Seeking an energetic and dependable analyst to perform routine testing to support process development and help progress programs through the pipeline. This individual will focus on molecular biology assays with a development opportunity to cross-train and support cell-based, potency, flow cytometry, separations and biophysical methods as well. This analyst will interface with many departments and projects necessary to complete tasks in a timely manner. | 7/25/2022 |
| 6367 | Exelixis Alameda, CA Scientist I, Compound Repository Scientist I, Compound Repository Scientist I, Compound Repository BS in related discipline Exp: one year |
The Scientist I, HTS is responsible for assisting in the development and completing the assay execution of both high throughput screening (HTS) campaigns in 1536-well plate format and weekly screening campaigns in 384-well plate format using the appropriate automation. | 7/25/2022 |
| 6368 | Exelixis Alameda, CA Scientist I (Pharmacology, Formulation) Master’s degree in a related chemistry, pharmaceutical sciences, biochemistry, biology discipline Exp: zero or more years |
The successful and highly motivated candidate will support the in vivo pharmacology research program to perform pre-formulation work, develop formulation study, execute analytical test methods, organize the data and summarize related reports. | 7/25/2022 |
| 6369 | Exelixis Alameda, CA Scientist I (Lead Discovery) Scientist I (Lead Discovery) Scientist I (Lead Discovery) BS in related discipline Exp: one year |
The Scientist I, HTS is responsible for assisting in the development and completing the assay execution of both high throughput screening (HTS) campaigns in 1536-well plate format and weekly screening campaigns in 384-well plate format using the appropriate automation. | 7/25/2022 |
| 6370 | Exelixis Alameda, CA Scientist II (Tumor Biology) Scientist II (Tumor Biology) Scientist II (Tumor Biology) BS/BA degree in related discipline Exp: one year |
We are looking for a Scientist for our Tumor Biology Department. The successful and highly motivated candidate will evaluate the activity of small molecule inhibitors in cell-based assays for oncology drug discovery. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. | 7/25/2022 |
| 6371 | Exelixis Alameda, CA Scientist II (ADC Biology) Scientist II (ADC Biology) Scientist II (ADC Biology) Bachelor’s degree in pharmacology or cancer biology or closely related discipline Exp: one (1) year |
Discovery Biotherapeutics is seeking an experienced, self-motivated Scientist II to provide in vitro pharmacology support for the advancement of the biologics portfolio at Exelixis. The successful candidate must have strong pharmacology background in cancer as he/she will support preclinical activities of ongoing and new biologics projects in antibody drug conjugates and bispecific antibodies. | 7/25/2022 |
| 6372 | Exelixis Alameda, CA Scientist II (Oncology Discovery) Scientist II (Oncology Discovery) Scientist II (Oncology Discovery) BS/BA degree in related discipline Exp: one year |
We are looking for a Scientist for our Tumor Biology Department. The successful and highly motivated candidate will evaluate the activity of small molecule inhibitors in cell-based assays for oncology drug discovery. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. | 7/25/2022 |
| 6373 | FloDesign Sonics Jaffrey, NH Process Engineer Bachelor’s Degree in Engineering (e.g., Manufacturing, Industrial, Mechanical, Design) Exp: 1+ years |
At Millipore Sigma the Process Engineer will work in a dynamic environment supporting the manufacture and testing of high purity filters with a focus on quality, process control/improvements, electro-mechanical assembly, and material handling. The successful candidate will be an enthusiastic team player with high energy and strong engineering skills. | 7/25/2022 |
| 6374 | FloDesign Sonics Danvers, MA Quality Engineer I Bachelor’s Degree in Engineering, Biology, Chemistry, or related field Exp: 1+ years |
As a Quality Engineer at MilliporeSigma in our Danvers, MA, production site, you play a key role in the success of the Quality and Manufacturing organizations. | 7/25/2022 |
| 6375 | FloDesign Sonics Tempe, AZ Analytical Chemist Master’s degree in Physics, Chemistry, or other Science discipline Exp: 1+ years’ |
EMD Electronics in Tempe, AZ is seeking a Chemist to join our Analytical Technology group. This group performs analysis and characterization of trace metals and nanoparticles used in CMP slurries for the semiconductor fabrication industry. | 7/25/2022 |
| 6376 | FloDesign Sonics St Louis, MO Associate Scientist Master’s Degree in Biology or Chemistry or Life Science field Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist you will conduct immunoassays and Research & Development related activities within the Life Science business. This individual could be responsible for several roles focusing on new product development, product validation, troubleshooting, and Operations support for key biological reagents. This is an excellent opportunity to gain experience in groundbreaking, high sensitivity assay technologies and new product development processes in the biotechnology industry and will report to the R&D Manager. | 7/25/2022 |
| 6377 | FloDesign Sonics Rockville, MD Associate Scientist 2 Bachelor’s degree in scientific field (i.e., Biology, Chemistry, etc.) Exp: 1+ years |
In this role, you will perform a wide variety of routine tasks to support the virus production team in the growth of regulatory compliant virus banks, under the oversight of the Scientist. You will be responsible for performing cell culture activities, virus growths, virus titration assays and virus decontamination procedures. The ability to maintain effective working relationships with support services, scientists and all laboratory personnel are critical for success in the role. | 7/25/2022 |
| 6378 | Flagship Biosciences Broomfield , CO Analyst I Bachelor’s degree in a scientific field and Exp: 0‐2 years |
The Analyst I, with team support, is the first line scientific resource responsible for delivery of analytical services, to include: generation of images, performance of image analysis related tasks, contribution to new analytical techniques and procedures, dispersal of project components to appropriate cross departmental resources, and providing feedback to drive project goals. The Analyst I must be eager to learn from and interact with colleagues at all levels of our organization, have a positive attitude and look for ways to continuously improve. The right fit for this position views collaboration and frequent communication as invaluable tools for building relationships and successfully accomplishing the goals. The Analyst I must be consistently flexible and be willing to adapt to rapidly changing priorities. | 7/27/2022 |
| 6379 | Galatea Surgical San Diego, CA Research Associate II Bachelor’s or Masters degree, in Biology or related scientific discipline. Exp: One to two years' |
The Research Associate II performs routine and complex laboratory tasks and procedures relevant to custom products and services in the Custom Technology Team. The Associate will perform a variety of routine experimental protocols and procedures to fulfill custom manufacturing requirements that include, but are not limited to formulations, experimental design, product testing/analysis, and results reporting. The Associate will work independently within generally defined procedures and practices in selecting methods and techniques for obtaining results. The Associate will observe and comply with safety standards and procedures and assist in general laboratory maintenance. Direction is both verbal and written. | 7/27/2022 |
| 6380 | Galatea Surgical San Diego, CA R&D Reagent Research Associate BS or BA degree in Molecular Biology, Chemistry, Biochemistry, or related subject area. Master’s degree preferred. Exp: 1 year |
BD is seeking a Reagent Research Associate to work within a team that develops new point-of-care assays for human in vitro diagnostic use. The Reagent Research Associate supports various R&D assay development teams and is principally responsible for the formulation, organization, and quality control of assay raw materials, amplification master mixes, buffers, and consumables. The associate applies good laboratory practice and analytical skills to manage the overall reagent inventory, and material output and works with other team members to resolve technical challenges. Works under the direction of Senior Reagent Scientists or above. | 7/27/2022 |
| 6381 | Genentech Carlsbad, CA RESEARCH ASSOCIATE I B.S. in Biochemistry, Molecular Biology, Analytical Chemistry or a related field Exp: 0 - 3 years |
You will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision. You will investigate, adapt or modify experimental methods and technologies for project advancement. A unique opportunity to leverage your background and skills in molecular diagnostics to enhance and build your career by working cross-functionally. An exciting career opportunity where your contributions will impact business opportunities through successful completion of projects. | 7/27/2022 |
| 6382 | GenScript Piscataway, NJ Associate Research Scientist, Sequencing Team Master degree in molecular biology related field Exp: 1 year |
We are looking for an associate research scientist for the Sequencing lab. This position will be focusing on high throughput DNA sequencing workflow during the gene synthesis process. | 7/28/2022 |
| 6383 | GenScript Redmond, WA Research Associate Bachelor's degree in molecular biology, chemistry, biochemistry, pharmaceutical science, chemical engineering or related field, Master is preferred Exp: 0-5 years |
GenScript is looking for a highly motivated and scientifically rigorous individual to join our RNA team for RNA delivery formulation and new RNA product research and development as Research Associate. This position will focus on developing novel lipid nanoparticle formulations for RNA delivery. | 7/28/2022 |
| 6384 | GenScript Piscataway, NJ Associate Research Scientist in Automated Gene Synthesis Team Master degree in molecular biology related field Exp: 1 year |
We are looking for an automation power user for the automated gene synthesis team. This position will be focusing on high throughput automated liquid handling and colony picking/ culturing during the gene synthesis process | 7/28/2022 |
| 6385 | Ginkgo Bioworks Boston, MA Cell Culture Associate (Cambridge Location) Bachelor’s degree Exp: 1+ year |
Coordinate with program teams to fulfill cell requests with a dedication to delivering quality work; Execute all aspects of mammalian cell culture for both suspension and adherent cells, including media preparation, culture initiation, propagation, and cryopreservation; Perform assays such as cell count, viability, doubling time, light microscopy, and expression of cell lineage markers by flow cytometry; Independently troubleshoot problems and propose solutions related to cell culture, diagnostic/QC assay design, and execution; Coordinate with teammates for material and task handoffs in order to deliver high-quality, trusted work; Maintain accurate experiment and inventory records in various internal databases; Establish and maintain a clean cell culture laboratory by practicing aseptic technique, adhering to equipment cleaning guidelines, and routinely testing and monitoring equipment and culture sterility; Execute internal development projects to increase capacity and onboard new capabilities for the Mammalian Operations team | 7/28/2022 |
| 6386 | Ginkgo Bioworks Boston, MA Cell Culture Associate (Seaport Location) Bachelor’s degree Exp: 1+ year |
Coordinate with program teams to fulfill cell requests with a dedication to delivering quality work; Execute all aspects of mammalian cell culture for both suspension and adherent cells, including media preparation, culture initiation, propagation, and cryopreservation; Perform assays such as cell count, viability, doubling time, light microscopy, and expression of cell lineage markers by flow cytometry; Independently troubleshoot problems and propose solutions related to cell culture, diagnostic/QC assay design, and execution; Coordinate with teammates for material and task handoffs in order to deliver high-quality, trusted work; Maintain accurate experiment and inventory records in various internal databases; Establish and maintain a clean cell culture laboratory by practicing aseptic technique, adhering to equipment cleaning guidelines, and routinely testing and monitoring equipment and culture sterility; Execute internal development projects to increase capacity and onboard new capabilities for the Mammalian Operations team | 7/28/2022 |
| 6387 | Ginkgo Bioworks Boston, MA Research Associate – Assay Development BS or MS in biology, biochemistry, bioengineering, pharmacology, or equivalent Exp: 1-2 years |
If you have interest in learning how to use cutting edge automation and software to understand, engineer and operationalize biology, perhaps a role as an HTS assay developer would be a good fit for your career. Ideally, you have experience in the development & optimization of biochemical assays and microbial plate culture. As an assay developer, you will design and execute laboratory experiments, generate & interpret data supporting the development of new processes and assays, and execute high-throughput screens. Other responsibilities will include learning about and applying new technical and scientific advances to your work, troubleshooting, data analysis, and reporting. Assay developers interact with and learn from many other teams at Ginkgo, so if you enjoy interdisciplinary work, assay development could be a great fit for you! | 7/28/2022 |
| 6388 | Ginkgo Bioworks Boston, MA Research Associate II, Molecular Biology BS or MS in biology, microbiology, genetics, or equivalent Exp: 1+ years |
We are seeking an inquisitive Research Associate II to join the Build team to help us run and improve our yeast genome engineering service. You will be responsible for amplifying, purifying and transforming DNA to create new strains for our program team. You are the ideal Build operator if you love working closely with a team in a fast paced environment to deliver high quality processes. We need your enthusiasm for accuracy and yeast biology, to help us meet our mission of making biology easier to engineer. Please consider applying even if you don\'t have all of the qualifications. | 7/28/2022 |
| 6389 | Global Pharma Tek Houston, TX Research Assistant II Bachelor’s Degree or Master’s Degree in Biological Sciences Exp: entry level years |
Client is seeking a highly motivated research associate to perform analytical support and assay qualification in the viral vector Research and Development team (R&D). The successful candidate will be proficient in viral vector characterization assays; perform assays transfer to process development team (PD); be able to analyze bioprocessing data, responsible for writing reports for Assay Qualification and Assay Validation. | 7/28/2022 |
| 6390 | Global Pharma Tek Salt Lake City, UT Scientist 1, Analytical Chemistry Development Associates degree or higher in a STEM major (Examples: Chemistry, biology, microbiology, biotechnology, biomedical engineering). Exp: 1-5 years |
Provide technical skill, analytical testing, and engineering support for design and development activities for various medical device products. Support current products in roles of quality, research & development, pilot-scale manufacturing, supply continuity, and cost improvement. Focus will be on in vitro testing using biological materials. An understanding / training in biology is a plus. Execute technical and cross-functional project | 7/28/2022 |
| 6391 | Gossamer Bio San Diego, CA Contract Research Associate, Biology B.Sc. in cell and molecular biology or related field Exp: 1-2 years |
This is for a contract role through end of 2022. We are seeking a highly motivated scientist/research associate to join the Biology Team to cover for leave of absence. This position will require excellent attention to detail and follow-through on the execution of established protocols as well as the opportunity to participate in the assay development process. The successful candidate will demonstrate a strong commitment to the rigor of scientific research within an industry setting as well as creativity in the form of critical thinking required for the interpretation of experimental data. | 7/28/2022 |
| 6392 | GRO Biosciences Cambridge, MA Research Associate/Sr RA, Chemistry Expansion MS degree (or BS/BA degree in biology, microbiology, biotechnology, biological engineering, or related field Exp: 1 year |
GRO Biosciences (GRObio) is hiring an RA/Sr RA with bench experience in molecular biology to advance the company’s recoded organism technology. Recoded organisms enable GRObio to generate revolutionary products of unprecedented structural and chemical diversity. With the tools at GRObio, you’ll be able to propose, develop, and implement completely differentiated solutions to longstanding, critical problems. The selected candidate for this position will work within the Chemistry Expansion division, enabling the scalable incorporation of new amino acids into proteins. Major job responsibilities include development and screening of translation machinery for new amino acids, and general engineering of ribosomal translation. Day-to-day activities include design and execution of experiments in conjunction with other team members. Diligence, transparent communication, and record keeping will be critical skills to enable success in this position. Your creativity and ingenuity will be crucial to driving GRObio’s research priorities optimizing strain performance and expanding the amino acid alphabet to create differentiated products. | 7/28/2022 |
| 6393 | GlaxoSmithKline Collegeville, PA Associate Analytical Scientist Bachelor’s degree Exp: 1-3 years |
As an Associate Analytical Scientist, you will progress analytical aspects of projects, utilizing your technical expertise as part of a product development and wider matrix teams. The candidate may engage with project teams and other stakeholders for various projects under different stages of development. The candidate may interact with other labs, internal and external to GSK, to support the training and transfer of analytical methods. | 7/28/2022 |
| 6394 | GlaxoSmithKline Collegeville, PA Associate Scientist BS degree in Pharmaceutics, Biology, Biochemistry, Chemistry, Chemical Engineering, or related scientific discipline Exp: 1 year |
As an Associate Scientist, you will join the Technology Advancement and Portfolio/Platform Support team within the Process Engineering and Analytics department of the Drug Product Development organization within the GSK R&D. You will primarily support drug product manufacturing process development using the small-scale capabilities, platform initiatives, combination product development, support technology transfers, and new technology implementation for new products in the pipeline. | 7/28/2022 |
| 6395 | GlaxoSmithKline King of Prussia, PA Biopharm Manufacturing Associate II BS/BA in life sciences/engineering or computer science/information systems. Exp: no previous experience |
As a Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. | 7/28/2022 |
| 6396 | GlaxoSmithKline Collegeville, PA Associate Scientist - Analytical BS or MS in Chemistry Exp: 1+ year |
As an Associate Analytical Scientist, you will progress analytical aspects of projects, utilizing your technical expertise as part of a product development team working with many partner groups. This role will provide YOU the opportunity to contribute to analytical development and to progress YOUR career. | 7/28/2022 |
| 6397 | GlaxoSmithKline Collegeville, PA Associate Scientist, Biology (Upper Providence, PA) Bachelor’s Degree in Biological Sciences (such as Cell Biology, Immunology, Oncology or Molecular Pharmacology) Exp: one year |
As an Associate Scientist, you will develop assays in primary cells and cell lines for immunology and oncology programs for use in high-throughput screening and mechanistic studies. This is an exciting, lab-based role that will allow the individual to contribute to early drug discovery programs through validation of novel targets and new chemical entities. The successful candidate is expected to be effective in designing and executing experiments at the highest possible scientific standard, be highly flexible and productive, and possess positive communication skills. | 7/28/2022 |
| 6398 | Harpoon Therapeutics South San Francisco, CA RESEARCH ASSOCIATE, PROTEIN PURIFICATION Bachelors Exp: 1-5 years |
We are seeking a highly motivated individual who enjoys detail-oriented technical work, can manage diverse responsibilities in the lab, and thrives in a fast-paced work environment. As an integral member of the Protein Science group, this individual will work closely with other team members within Protein Science and partner with other functional areas in the organization. The ideal candidate will have strong technical aptitude for lab and instrumentation work, and a flexible problem-solving mindset | 7/29/2022 |
| 6399 | Heska Des Moines, IA Technician I, II or III, Bacterins Bachelor’s Degree in a science or bio-technology field. Exp: 1 year |
The Bacterins Technician I, II or III will work under the close supervision of the Bacterins supervisor to foster the growth of bacterial cultures through fermentation and cell media preparation while maintaining a sterile environment. This position requires the ability to multi-task and follow standard operating procedures. Position level will be based on experience. | 7/29/2022 |
| 6400 | Champions Oncology Rockville, MD Research Technician I, Surgical Services Research Technician I, Surgical Services Research Technician I, Surgical Services BS degree in biology, pharmacology, or related field Exp: 1 year |
Support in vivo oncology studies in mice as a member of the Surgical Services team. Duties and responsibilities are: Handle, restrain, and provide care for all animals; Observe animals for general health and overall well-being; Receive, characterize and orthotopically or heterotopically surgically implant tissue samples; Provide perioperative and intraoperative animal care; Conduct tumor volume measurements and sample collection for in vitro characterization; Perform preparation activities, including collection tube labeling and room set-up; Perform blood collection, processing and sample storage; Perform various subcutaneous injections; Collect, document, and maintain tissue samples within database as well as the tumor bank; Conduct and record data in compliance with Standard Operating Procedures (SOPs); Record data using laboratory information management systems; Work weekend and holidays as needed | 7/18/2022 |
| 6401 | Champions Oncology Rockville, MD Research Technician I, Study Services BS/MS degree in biology, pharmacology, or related field Exp: 1 year |
As a Research Technician in Study Services, you will support in vivo oncology studies in mice. Additional duties and responsibilities include: Perform in-life technical procedures, handle, restrain, and provide care for all animals; Observe animals for general health and overall well-being; Administer therapeutic agents by various routes; Provide animal welfare assessments, including body weight and tumor volume measurement; Allocate animals to study and non-study groups; Provide preoperative animal care; Euthanize animals as directed in study protocols and directives; Read study protocols and extract pertinent information; Perform study preparation activities including collection tube labeling and room/BSC set-up; Record data using laboratory information management systems; Work weekends and holidays on rotating basis | 7/18/2022 |
| 6402 | Champions Oncology Rockville, MD Research Technician, Necropsy BS degree in biology, pharmacology, or related field Exp: 1 year |
Primary objective: to support the in vivo oncology studies in mice as well as properly euthanize animals in accordance to the company standards and regulations. | 7/18/2022 |
| 6403 | Companion Medical Memphis, TN Microbiologist-Sterilization I Bachelor's degree in Science or technical field Exp: 0+ years |
In this exciting role as a Microbiologist-Sterilization I you will have responsibility to work on assignments that are complex in nature where judgment and initiative are required in resolving problems and making recommendations. Provides input to Supervisor of Microbiology regarding sterilization, testing and technical issues. Works with the contract sterilizers to maintain sterilization cycles using either Gamma Sterilization or Ethylene Oxide Sterilization in accordance with all industry, Federal and international guidance documents/regulations. Interacts with the Regulatory, Quality, Packaging and R&D Engineering in Memphis to maintain the microbiological specifications and test plans necessary to ensure compliance with the overall Quality Requirements. Assists with microbiological and sterilization issues affecting manufacturing. Serves as consultant for laboratory on technical issues. Develops procedures for laboratory testing. Moderate supervision | 7/18/2022 |
| 6404 | Companion Medical Brooklyn Park, MN Microbiologist-Sterilization I Bachelor's degree in Science or technical field Exp: 0 years |
In this exciting role as a Microbiologist/Sterilization I you will have responsibility to support and improve the sterility assurance program for Medtronic's Extra Corporeal Therapies device portfolio. You will focus on the sterilization process, cleanroom technology, and general microbiology for products produced at the Brooklyn Park, Minnesota site. In this position, you will be responsible for monitoring the sterility assurance program and driving timeliness of critical compliance imperatives such as requalifications and product lifecycle change management tasks. This role will also collaborate with other Medtronic global sterility assurance partners to harmonize best practices for cleanroom, microbiology, and sterilization methodologies. | 7/18/2022 |
| 6405 | Companion Medical Fridley, MN Analytical Instrument Specialist Bachelor's in Chemistry, Biology, Engineering or other Science or technical field. Exp: 0+ years |
In this exciting role as an Analytical Instrument Specialist you will have the responsibility for performing routine instrument qualification and maintenance for the Chemistry and Microbiology Laboratories. The candidate will be required to perform planned preventative maintenance and requalification activities. In addition, they will also be expected to perform non-routine instrumentation troubleshooting activities and revise Instrument Operating Procedures (IOPs) to ensure that all maintenance, calibration, and training activities are properly documented and governed. This individual will work in conformance with company policies and current Good Manufacturing Practices, Good Lab Practices (GLP), regulatory requirements and standards to meet quality and accuracy requirements. | 7/18/2022 |
| 6406 | Companion Medical Mounds View, MN Materials Engineer I Bachelor's Degree in materials, chemical, biomedical or mechanical engineering Exp: 0+ years |
This position will support product and materials development for new and released product, ensuring product safety and reliability through the direction and execution of characterization testing. This will include providing problem solving, materials laboratory testing and data analysis in support of new and existing implantable biomedical devices and systems. Biocompatibility and biostability testing, as well as documenting product equivalence through appropriate characterization testing will also be included. | 7/18/2022 |
| 6407 | Companion Medical Mounds View, MN Software Engineer I Bachelor’s degree in Software Engineering, Computer Science, or related technical field. Exp: 1+ years |
As a Software Engineer I in the Cardiac Rhythm Management (CRM) R&D Software Organization, the individual will operate in all phases and contribute to all activities of the software development and verification process. The CRM Medtronic Application Services (MAS) team leverage various software technologies to create, enhance, and maintain Web/Mobile based Patient Management Software System used by our clinicians and patients. The CRM MAS team is looking for a proactive, self-starting, strong software development engineer. | 7/19/2022 |
| 6408 | Companion Medical Mounds View, MN Reliability Engineer I Bachelors degree in Engineering, Science or technical field Exp: 0 years |
The Reliability Engineer will work in a fast-paced environment, partnering closely with Design/R&D, manufacturing, and Regulatory Affairs. This role serves as a technical representative for the Reliability function, ensuring full compliance of the final product. | 7/19/2022 |
| 6409 | Cook Biotech West Lafayette, IN Biocompatibility Scientist Master's degree in Toxicology, Biology, Biomedical Engineering, Material Science, or related field required Exp: 1 year |
The Biocompatibility Scientist at Cook is responsible for assessing the safety of devices and related materials, assisting with writing risk assessments of medical devices, and ensuring the Cook device testing program is compliant to national and international regulatory guidelines. | 7/19/2022 |
| 6410 | CooperSurgical Tucson, AZ Blood/Tissue Sample Processing Technician I - Tucson, AZ Bachelor’s degree in one of the biological, chemical, or physical sciences OR Bachelor’s degree in a different science Exp: 1 year |
Position Summary: The Blood/Tissue Sample Processing Technician I (Hematology) is responsible for analyzing and documenting test results from our cord blood and cord tissue processed samples using standard hematology techniques as dictated by our quality management system while maintaining the highest quality services possible. This position is also responsible for releasing raw materials, supporting the analytical and processing equipment maintenance program, and providing our internal customers with technical expertise while maintaining the highest quality services possible. | 7/19/2022 |
| 6411 | Covaris Woburn, MA Research Associate – Applications Development Master’s Degree in biology, chemistry, biomedical engineering, or biochemistry Exp: 0-2 years |
This hands-on position offers an exciting opportunity in the life sciences to discover, develop, and evaluate new product ideas, enhancements to existing products, or strategic product extensions, and translate research into usable and marketable products. This position involves collaboration in a multi-disciplinary team composed of biologists, chemists, and mechanical and electrical engineers. This position will function as a member of the Applications Team reporting to a Senior Applications Scientist. | 7/19/2022 |
| 6412 | Crown Bioscience San Diego, CA Research Associate I, In Vivo Oncology Research Associate I, In Vivo Oncology Research Associate I, In Vivo Oncology Bachelor’s Degree in a scientific discipline Exp: One year |
In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 7/19/2022 |
| 6413 | Crown Bioscience San Diego, CA Research Associate I, In Vivo Oncology Research Associate I, In Vivo Oncology Research Associate I, In Vivo Oncology Bachelor’s Degree in a scientific discipline Exp: One year |
The In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 7/19/2022 |
| 6414 | Crown Bioscience San Diego, CA Research Associate I, Autoimmune & Inflammatory Diseases, Pre-Clinical Associate's degree or Bachelor's or Master's degree in Biology, Biotechnology or other relevant area of scientific discipline Exp: 1-2 year(s) |
The purpose of the Inflammation and Immunology Research Associate I position is to perform primarily in vivo animal studies within the Inflammation and Immunology group in support of the Company's goals and objectives. | 7/19/2022 |
| 6415 | Crown Bioscience San Diego, CA Research Associate I, Cancer Biology & Immunology Bachelor's degree in Biology, Biotechnology or other relevant area of scientific discipline. Exp: 1‐ 2 years |
The purpose of the Cancer Biology & Immunology Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 7/19/2022 |
| 6416 | Crown Bioscience San Diego, CA Research Associate I, Cell Support Research Associate I, Cell Support Bachelor's degree in Biology, Biochemistry or related area. Exp: 1-2 years |
The purpose of the Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 7/19/2022 |
| 6417 | CryoLife Kennesaw, GA R&D Engineer I BS Degree in Biomedical or Mechanical Engineering Exp: 0 - 2 years |
Advance the development of novel medical devices from initial concept through in vivo characterizations. The position will focus on the prototyping, characterization, testing, and refinement of subcomponents of medical devices. | 7/19/2022 |
| 6418 | CryoLife Kennesaw, GA Process Engineer Bachelor’s degree in Engineering (Mechanical, Chemical, Biomedical, Industrial or related field of engineering) Exp: 0-2 years |
Responsible for providing process engineering support for all product manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as develop new processes to improve manufacturing efficiency. Supports new product launches by collaborating with other functional areas and providing process engineering expertise during the implementation of processes or equipment. | 7/19/2022 |
| 6419 | Culture Biosciences South San Francisco, CA Lab Technician Associates/Bachelors Exp: 0 year |
Culture Biosciences is hiring for multiple Lab Technicians to support our lab operations, prepare media and run assay testing on client samples. This is an excellent opportunity to learn more about the inner workings of our cloud lab environment, gain valuable experience with operations, media prep, and wet lab skills. We’re motivated to hire those who are eager to learn and excited by the technology we have developed. | 7/20/2022 |
| 6420 | Cyprotex Watertown, MA Research Associate and/or Research Assistant - Toxicology BS/ MS in a relevant bio scientific discipline Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays | 7/20/2022 |
| 6421 | Cytovance Oklahoma City, OK ANALYTICAL DEVELOPMENT ASSOCIATE BS/MS in a life science field Exp: BS: 1+ years; MS: 0+ years |
The AD Associate position develops, optimizes, and qualifies analytical methods for biopharmaceutical products. The associate also supports drug development departments, such as Purification Department and Cell Culture Department, by performing analytical testing. | 7/20/2022 |
| 6422 | Cytovance Oklahoma City, OK PD ASSOCIATE - UPSTREAM - MICROBIAL Bachelor’s degree in a life science field Exp: 0-3 years |
The Process Development Associate I conducts laboratory experiments as part of development and/or demonstration of processes related to cell expansion (mammalian or microbial) of biopharmaceutical products. The Associate also participates in activities related to the maintenance and upkeep of the Process Development Lab. | 7/20/2022 |
| 6423 | Demetrix Berkeley, CA Associate Scientist – Plate Model Development Bachelor of Science degree in biological system engineering, biochemistry, microbiology, or related field Exp: 0 to 2 yr |
You will be part of the High Throughput & Process Engineering team and play a key role in the development of novel microbial strains. You will be part of an interdisciplinary team of fermentation/DSP scientists and engineers, automation engineers, software engineers, analytical chemists, and molecular biologists working to rapidly develop microbial strains to produce natural product medicines . In this role, you will work in a highly collaborative fashion with strain and fermentation engineers to screen novel microbial strains and processes in a high throughput manner. This includes designing and executing experiments, analyzing results, troubleshooting deviations, maintaining a high standard of data integrity, and clearly communicating findings cross-functionally. | 7/20/2022 |
| 6424 | DiaCarta Richmond, CA Research Associate S. degree in molecular biology or a related field Exp: 0-2 |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 7/20/2022 |
| 6425 | DiCE Molecules South San Francisco, CA Research Associate/Sr. Research Associate, In Vitro Pharmacology B.S. degree in biochemistry, biology, or a related field Exp: 1-4 years |
The successful candidate will be responsible for planning and independently performing experiments using a wide range of in vitro assays and technologies. These will include biochemical/biophysical and mammalian cell culture assays, and will expand over time. This person will support cutting-edge small molecule discovery through their data and analysis within a growing multidisciplinary team. | 7/20/2022 |
| 6426 | Distributed Bio S. San Francisco, CA Research Associate 1 - In Vivo PK Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline. Exp: Zero to three years |
The individual in this position will be involved in all aspects of studies supporting the biotechnical services group. This position is hands-on with responsibilities including, but not limited to animal husbandry, animal handling and restraint, administration via various routes, clinical observations, sample collection and processing, and accurate data collection. | 7/20/2022 |
| 6427 | Distributed Bio S. San Francisco, CA Research Associate I - In Vivo, CNS 1 1 1 1 Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline. Exp: Zero to three years |
The individual in this position will be involved in all aspects of studies supporting the biotechnical services group. This position is hands-on with responsibilities including, but not limited to animal husbandry, animal handling and restraint, administration via various routes, clinical observations, sample collection and processing, and accurate data collection. | 7/20/2022 |
| 6428 | Distributed Bio Ashland, OH Research Assistant 1 (Bioanalytical Chemistry) Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline Exp: Zero to two years |
We are seeking a Research Assistant I for our Safety Assessment Group site located in Ashland, Ohio. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples, and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods | 7/21/2022 |
| 6429 | Distributed Bio Mattawan, MI Research Analyst 2 - Bioanalytical Bachelor’s degree (BA/BS) or equivalent experience. Exp: 1 year |
We are seeking an Research Analyst 2 for our Bioanalytical Chemistry team at the site located in Mattawan, MI. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 7/21/2022 |
| 6430 | Distributed Bio Spencerville, OH Research Technician Assistant (Entry Level) Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months to 1 year |
Performs technical tasks in the conduct of in vivo research studies or support services in accordance with good animal welfare practices. Prepares, collects and records research data and specimens in compliance with applicable regulations and SOPs. We are seeking an experienced Research Technician I for our InVivo (InLife) Team within our Safety Assessment site located in Spencerville, OH. The following are responsibilities related to the Research Technician 1: The Research Technician 1 will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. We are looking for 1st and 2nd shift. 2nd shift does include 10% pay differential M-F 2:30pm-11pm. 1st shift 7am-330pm w/ rotating weekend/month & rotating holidays. | 7/21/2022 |
| 6431 | Distributed Bio S. San Francisco, CA Research Associate I - In Vivo, CNS 1 1 1 Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline. Exp: Zero to three years |
The individual in this position will be involved in all aspects of studies supporting the biotechnical services group. This position is hands-on with responsibilities including, but not limited to animal husbandry, animal handling and restraint, administration via various routes, clinical observations, sample collection and processing, and accurate data collection. | 7/21/2022 |
| 6432 | EAG Laboratories San Diego, CA Cell Biology Associate Bachelor’s degree in biology, biochemistry, molecular biology or similar discipline Exp: 1 or more years |
Eurofins Lancaster Laboratories PSS is searching for a Cell Biology Associate Associate to work in San Diego, CA. Our client is looking to expand its capabilities in biochemical and immunological assays applied to immunology/immunogenicity. We are looking for a highly motivated and agile biochemist. Your contributions may include independently design and perform experiments with the goal of understanding and assessing immunogenicity of biological drugs, and ultimately to generate datasets to inform predictive models of antigen-specific immune response. | 7/21/2022 |
| 6433 | EAG Laboratories San Diego, CA Molecular Biology Associate B.S. in Biological sciences (Molecular Biology, Biotechnology, Immunology, Biochemistry, or similar field) Exp: 1-3 years |
Eurofins Lancaster Laboratories PSS is searching for a Molecular Biology Associate to work in San Diego, CA. | 7/21/2022 |
| 6434 | EAG Laboratories San Diego, CA MSAT Engineer Bachelor's degree in chemistry, microbiology, biology, engineering, computer science, or other related degree concentration Exp: One year |
Applies GMP/GLP in all areas of responsibility, as appropriate; Demonstrates and promotes the company vision; Regular attendance and punctuality; Compliance - Stay current with client, regulatory, validation, IT, and e-record compliance regulations, and requirements. Ensure projects are completed in compliance with existing quality systems. Provide support to implement new quality systems and programs; Research - Assist with research of instrumentation with information obtained from vendors, manuals, and other resources to introduce duplicate/similar instruments and software. Assist with integration of instrumentation into existing data center environments and workflows; Technical Writing - Author validation deliverables in accordance with established validation program. Assist with developing/enhancing instrumentation procedures. Training - Provide guidance and coaching within a team environment. Provide training to technical groups; Validation Support - Accurately update validation program components and maintain LIMS instrument database entries. Perform periodic review for chambers and compile and assist with periodic review of computerized systems. Generate monitoring, trending, and departmental reports. Perform routine project close out activities. | 7/21/2022 |
| 6435 | EAG Laboratories San Diego, CA Research Associate I Bachelor’s degree in life sciences or related discipline Exp: 1+ years |
Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. Join Eurofins Beacon Discovery part of the Eurofins Discovery ™ group of companies serving global clients in the Pharma and Biotech industries. Work alongside industry experts and collaborate with team members to directly and positively impact human health worldwide! We have a philosophy to support work life balance, career progression opportunities and offer many benefits such as formal mentoring programs, tuition reimbursement, extensive career training programs, competitive health benefits, paid time off and 10 annual paid holidays*. | 7/21/2022 |
| 6436 | EAG Laboratories San Diego, CA Protein Purification Associate Bachelor's degree Exp: 1-3 years |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a Protein Purification Associate to support our Professional Scientific Services group in San Diego, CA. | 7/21/2022 |
| 6437 | Elektrofi Boston, MA Research Associate/Intern BS (Associate) or Junior/Senior (Intern) in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biology, Bioengineering, or a related field Exp: |
Elektrofi is looking for a Research Associate to join a team responsible for the development of platform formulations for Elektrofi’s proprietary microparticle production process. The Research Associate will play a key role in supporting the development of its biologics formulation platform. This individual will join an earlystage, multidisciplinary team of scientists and contribute to a variety of formulations activities in a highly collaborative environment | 7/21/2022 |
| 6438 | EMD Serono Jaffrey, NH Process Engineer Bachelor’s Degree in Engineering (e.g., Manufacturing, Industrial, Mechanical, Design) Exp: 1+ years |
At Millipore Sigma the Process Engineer will work in a dynamic environment supporting the manufacture and testing of high purity filters with a focus on quality, process control/improvements, electro-mechanical assembly, and material handling. The successful candidate will be an enthusiastic team player with high energy and strong engineering skills. | 7/21/2022 |
| 6439 | Millipore St. Louis, MO Associate Scientist Master’s Degree in Biology or Chemistry or Life Science field Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist you will conduct immunoassays and Research & Development related activities within the Life Science business. This individual could be responsible for several roles focusing on new product development, product validation, troubleshooting, and Operations support for key biological reagents. This is an excellent opportunity to gain experience in groundbreaking, high sensitivity assay technologies and new product development processes in the biotechnology industry and will report to the R&D Manager. | 7/21/2022 |
| 6440 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technologist (FT, 40 Hours) Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 7/11/2022 |
| 6441 | BioReference Laboratories Newark, NJ Medical Technician/Technologist (FT, 40 Hours) Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 7/11/2022 |
| 6442 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technologist (FISH) Sign-On Bonus Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 7/11/2022 |
| 6443 | BioReference Laboratories Houston, TX Lead, Medical Technologist (FT, 40 Hours) Bachelor degree in medical technology, chemistry, biology, or related life science Exp: 1 year |
The Molecular STI Laboratory Lead Technologist will perform complex chemical, biological, testing in the detection, diagnosis, prognosis, and treatment of disease. The Lead Medical Laboratory Technologist will work collaboratively with the laboratory team to provide testing services to the clients. Additional tasks can be assigned at the discretion of the Supervisor/Manager/Director. | 7/11/2022 |
| 6444 | BioReliance [Merck KGaA] St Louis, MO Associate Scientist Master’s Degree in Biology or Chemistry or Life Science field Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist you will conduct immunoassays and Research & Development related activities within the Life Science business. This individual could be responsible for several roles focusing on new product development, product validation, troubleshooting, and Operations support for key biological reagents. This is an excellent opportunity to gain experience in groundbreaking, high sensitivity assay technologies and new product development processes in the biotechnology industry and will report to the R&D Manager. | 7/11/2022 |
| 6445 | BioReliance [Merck KGaA] Rockville, MD Associate Scientist 2 Bachelor’s degree in scientific field (i.e., Biology, Chemistry, etc.) Exp: 1+ years |
We have an exciting opportunity for an Associate Scientist 2 to join our global virus production team based in Rockville, Maryland. In this role, you will perform a wide variety of routine tasks to support the virus production team in the growth of regulatory compliant virus banks, under the oversight of the Scientist. You will be responsible for performing cell culture activities, virus growths, virus titration assays and virus decontamination procedures. The ability to maintain effective working relationships with support services, scientists and all laboratory personnel are critical for success in the role. | 7/11/2022 |
| 6446 | BioReliance [Merck KGaA] Rockville, MD Associate Scientist 1 Bachelor’s Degree in scientific discipline (ie. Biology, Chemistry etc.) Exp: 0-1 years |
As an Associate Scientist 1 your activities will support assay development through commercial application of new and innovative service offerings within the biosafety testing space. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position. | 7/11/2022 |
| 6447 | BioReliance [Merck KGaA] Tempe, AZ Chemist I Bachelor’s Degree in Chemistry, or similar Scientific field Exp: 1+ years |
We are currently seeking a Laboratory Technician at MilliporeSigma for the Process and Technology Group within MilliporeSigma Operations. As a part of this organization, the successful candidate will be a team member and perform laboratory tasks independently. This position will be based at the Bedford, MA campus. | 7/11/2022 |
| 6448 | BioReliance [Merck KGaA] Bedford, MA Lab Technician II Bachelor's degree in Biology, Chemistry, Biochemistry or other Science Exp: 1 year |
As an Associate Scientist/Molecular Biologist within our Next Generation Sequencing (NGS) group in our Rockville, Maryland facility, your activities will support commercial biosafety testing within the organization, specifically using NGS platforms. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/ documentation and ensure all documentation fulfills generally accepted professional/ industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position. Your primary responsibilities will be to provide support for the day to day operation of the facility and to contribute to the timely execution of NGS service offerings for our customers. You will liaise closely with laboratory management, bioinformatics and support staff to ensure internal and external expectations are met or exceeded. You will be responsible for performing custom and routine NGS testing in accordance with all SOPs and regulations (cGMP and GLP). You will be expected to lead by example and work collaboratively to advance the application of NGS in the field of biosafety testing. | 7/11/2022 |
| 6449 | BioReliance [Merck KGaA] Rockville, MD Associate Scientist 2 Bachelor’s degree in scientific field (i.e. Biology, Chemistry, etc.) Exp: 1+ years |
As an Associate Scientist/Molecular Biologist within our Next Generation Sequencing (NGS) group in our Rockville, Maryland facility, your activities will support commercial biosafety testing within the organization, specifically using NGS platforms. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/ documentation and ensure all documentation fulfills generally accepted professional/ industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position. Your primary responsibilities will be to provide support for the day to day operation of the facility and to contribute to the timely execution of NGS service offerings for our customers. You will liaise closely with laboratory management, bioinformatics and support staff to ensure internal and external expectations are met or exceeded. You will be responsible for performing custom and routine NGS testing in accordance with all SOPs and regulations (cGMP and GLP). You will be expected to lead by example and work collaboratively to advance the application of NGS in the field of biosafety testing. | 7/11/2022 |
| 6450 | LGC Biosearch Technologies Charleston, SC Production Chemist (40820) Bachelor of Science degree, chemistry preferred Exp: 0-2 years |
The production chemist is responsible for the manufacturing of reference standard solutions by following routine procedures and operations of laboratory equipment. This is a highly collaborative position and requires a great sense of teamwork and productivity. We are looking for individuals that can thrive in a fast-paced laboratory setting and demonstrate ability to prioritize and organize work with guidance from team leads and supervisor. Our site manufactures both catalog and custom solutions for customers requiring focused bench work, detailed record keeping and flexibility in daily tasks. | 7/11/2022 |
| 6451 | LGC Biosearch Technologies Petaluma, CA Therapeutic Production Chemist I - Night Shift (42683) Bachelor of Science in a relevant STEM field Exp: 1 or more years’ |
The Therapeutic Production Chemist I perform routine oligonucleotide manufacturing processes in the LGC Biosearch Technologies’ Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophlization of oligonucleotides. | 7/12/2022 |
| 6452 | LGC Biosearch Technologies Petaluma, CA Therapeutic Production Chemist I - Weekend Shift (42684) BS. in a relevant STEM field Exp: 1 or more years’ |
The Therapeutic Production Chemist I perform routine oligonucleotide manufacturing processes in the LGC Biosearch Technologies’ Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophlization of oligonucleotides. | 7/12/2022 |
| 6453 | Bio-techne Minneapolis, MN Research Associate - Quantikine Assay Development Bachelor’s degree in Chemistry, Biology or related field required Exp: up to 3 years |
The major responsibilities of this position are to develop plate-based ELISA products related to Bio-Techne's existing product lines by identifying and optimizing components to meet product performance benchmarks. Primary activities will center on assay feasibility and optimization, reagent evaluation, data analysis, literature review, stability studies and product transfer. | 7/12/2022 |
| 6454 | Bio-techne Minneapolis, MN Advanced Research Associate Master’s degree in a related field Exp: up to 2 years |
This position is responsible for participating in the development of Bio-Techne's various product lines. You will maintain knowledge of multiple products and procedures as well as draft and revise standard operating procedures in order to further the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 7/12/2022 |
| 6455 | Bio-techne Newark, CA Research Associate, R&D BS in molecular biology, biochemistry, cell biology or related field Exp: 1 year |
We seek a highly motivated and creative research associate to join our R&D team. You will work within a highly dynamic group and be responsible for improving current products and developing new products based on RNAscope technology. | 7/12/2022 |
| 6456 | bioTheranostics [Hologic] San Diego, CA Entry Level Investigation Specialist B.S. in Molecular Biology, Microbiology, Chemistry, Biochemistry or Bioengineering/Biomedical Engineering Exp: 0-2 years |
Duties and Responsibilities: The incumbent may be asked to perform other function-related activities in addition to the below-mentioned responsibilities as reasonably required by business needs. Performs amplification based diagnostic assays Performs applicable internal analytical and performance testing methods used in Customer Product Support Assists with troubleshooting experimentation required for projects/investigations Trains new laboratory personnel on basic laboratory tasks. Operates basic laboratory equipment with safety mindset. General laboratory maintenance.. Assists in writing and executing protocols and reports for experimentation and qualifications as appropriate. Performs/assists with, simple to moderate investigations and prepares investigation reports/risk assessment statements as appropriate. Perform simple data analysis as required. Uses appropriate root cause analysis and lab investigation tools/process when performing investigations.Duties and Responsibilities: | 7/12/2022 |
| 6457 | Calico South San Francisco, CA Research Associate/Senior Research Associate, Proteomics BS Exp: 0-5 years |
Calico is seeking an experienced Research Associate/Senior Research Associate to join the mass spectrometry proteomics group. To succeed, you will need to be an enthusiastic team player, detail-oriented, organized and comfortable working on complex problems. We are looking for someone with detailed knowledge of proteomics and biochemistry techniques, and with demonstrated hands-on application. This is a hands-on bench position, focused on sample preparation, method development, instrument maintenance, troubleshooting and data analysis. The successful candidate will work with a large number of samples for collaborative projects, optimize and develop methods, as well as be responsible for smaller research projects. | 7/13/2022 |
| 6458 | Cambrex Durham, NC Associate Scientist II (Biopharma) Masters degree in Chemistry, Biochemistry, Molecular Biology or similar Exp: 1+ years |
As an Associate Scientist II in the biopharmaceutical team, you will work with a dynamic group of scientists supporting analytical method development, phase-appropriate validation, and testing services for viral/cellular based therapies and large molecules. | 7/13/2022 |
| 6459 | Cambrex Durham, NC Associate Scientist II (QC) MS life sciences degree Exp: 0- 1+ years |
As an Associate Scientist II in the Cambrex Quality Control team, you will be responsible for routine and non-routine cGMP testing of starting materials, drug substance, drug product, and reference standards for small molecule programs in late-phase clinical development and commercial. | 7/13/2022 |
| 6460 | Advanced Sterilization Products [Johnson&Johnson] San Diego, CA Associate Scientist I, Neuroimmunology Master's Degree in Pharmacology, Neuroscience, or Biology Exp: 1 to 3 years |
We are seeking a highly motivated Associate Scientist with in-vivo neuropharmacology experience to join our Neuroimmunology Discovery research team. The candidate should be passionate about the discovery and development of novel therapeutics for CNS disorders. Experimental work will be the core job function and as such the ideal candidate will spend close to full time at the bench generating data. It is critical that the successful candidate enjoys bench science, is scientifically curious, is self-motivated, but also a strong standout colleague, and can demonstrate a high level of efficiency. Strong interpersonal skills, the ability to interact well with peers and collaborators, and strong written and oral communication skills are vital to success in this role. To be successful in the position, the candidate must be organized, and practice good laboratory principles including detailed notebook entry of experiments.We are seeking a highly motivated Associate Scientist with in-vivo neuropharmacology experience to join our Neuroimmunology Discovery research team. The candidate should be passionate about the discovery and development of novel therapeutics for CNS disorders. | 7/13/2022 |
| 6461 | Advanced Sterilization Products [Johnson&Johnson] Spring House, PA Associate Scientist, Bioconjugates, RNA & Targeted Therapeutics M.S. degree in Chemistry, Biochemistry, Chemical/Biomedical Engineering or other related field Exp: 1 year |
In this position, the Associate Scientist will contribute to the development of various targeted therapeutics such as nucleic acid conjugates (siRNA, antisense, etc.), peptide/small molecule conjugates, or antibody conjugates. This scientist will work closely with team members to assist in the design of novel bioconjugates. S/he will primarily be responsible for the conjugation, purification, and analytical characterization of these molecules. S/he will also be responsible for routinely analyzing, interpreting, summarizing, and communicating experimental data. Additional responsibilities may include laboratory duties such as instrument and inventory maintenance. | 7/13/2022 |
| 6462 | Advanced Sterilization Products [Johnson&Johnson] Malvern, PA Associate Scientist, Large Molecule Drug Product Development M.S. degree in Engineering (Biomedical, Bioengineering, Chemical, Electrical or Mechanical) or related field Exp: 1 year |
The Associate Scientist in Large Molecule (LM) Drug Product Development (DPD) will work independently and in conjunction with development teams to support program/project needs. The candidate will also independently be accountable to lead, design, perform, and analyze studies in the development and engineering space in support of process and fill-finish activities for large molecules (e.g. monoclonal antibodies, fusion proteins, bi-specifics, gene therapies, cell therapies etc). | 7/13/2022 |
| 6463 | Advanced Sterilization Products [Johnson&Johnson] San Diego, CA Associate Scientist II MS degree in Biology, Immunology, Pharmacology, Immune-oncology or related discipline is required. Exp: 1-3 years |
The Associate Scientist will be a member of the Immunology Discovery group/Innate Immunity and function in a fast paced, highly matrixed and interactive environment. This group is focused on discovering novel therapeutics to treat various diseases including inflammatory and autoimmune diseases. | 7/13/2022 |
| 6464 | Advanced Sterilization Products [Johnson&Johnson] La Jolla, CA Associate Scientist, Discovery Chemistry (Multiple Openings) - La Jolla, CA Master’s Degree in synthetic organic or medicinal chemistry, or to be completed within 6 months, is required Exp: 1+ years |
We are seeking an experienced Bachelor’s- or Master’s-level medicinal chemist with excellent organic synthesis expertise to advance small molecule drug discovery programs toward the clinic. In this laboratory-based position, the successful candidate will partner with both internal and external medicinal chemistry teams to generate innovative solutions to synthetic and medicinal chemistry challenges within the context of small molecule drug discovery projects. They will maintain close interactions with computer assisted design scientists and biologists. Strong communication skills and the ability to thrive in a team and goal-driven environment are key attributes. This individual must also excel in communication and have strong interpersonal skills necessary to influence in a collaborative multidisciplinary environment.We are seeking an experienced Bachelor’s- or Master’s-level medicinal chemist with excellent organic synthesis expertise to advance small molecule drug discovery programs toward the clinic. In this laboratory-based position, the successful candidate will partner with both internal and external medicinal chemistry teams to generate innovative solutions to synthetic and medicinal chemistry challenges within the context of small molecule drug discovery projects. They will maintain close interactions with computer assisted design scientists and biologists. Strong communication skills and the ability to thrive in a team and goal-driven environment are key attributes. | 7/13/2022 |
| 6465 | Caris Life Sciences Tempe, AZ Research Associate - IV Research Associate - IV Bachelor’s or Master’s degree in a science field required. Exp: BS: 0-6 years; MS: 0-4 years |
Research Associates (RAs) are responsible for performing lab experiments utilizing various techniques that include, but are not limited to, Tissue (Cell) Culture, Cell Growth and Viability Assays, Immunohistochemistry (IHC), Immunocytochemistry (ICC), Cytotoxicity Assays, Gel Electrophoresis, SDS-PAGE, Western Blot, ELISA, Protein Extraction and Purification, in vivo and in vitro protein-protein crosslinking, Bioconjugation, Protein Enzymatic Digestion, Sample Preparation for HPLC and Mass Spectrometry. Furthermore, RAs are responsible for equipment maintenance, laboratory inventory, sample tracking, ordering supplies, receiving packages, and training other Research Associates. This position works under the direction of an associate research scientist, research scientist, senior research scientist, director of R&D or VP of R&D and follows standard laboratory procedures and policies. | 7/13/2022 |
| 6466 | Caris Life Sciences Phoenix, AZ Research Associate I Research Associate I Bachelor’s or Master’s degree in a science field required. Exp: 1 year |
Research Associate (RA) is responsible for performing blood processing as a member of the Biorepository. Furthermore, RAs are responsible for equipment maintenance, laboratory inventory, sample tracking, ordering supplies, receiving packages, and training other Research Associates. This position works under the direction of the Biorepository Manager and follows standard laboratory procedures and policies. | 7/13/2022 |
| 6467 | Caris Life Sciences Tempe, AZ Research Associate IV Bachelor’s or Master’s degree in a science related field is required. Exp: 0-6 years |
The successful candidate will be responsible for performing various techniques in the R&D lab. | 7/13/2022 |
| 6468 | Catalent Rockville/Gaithersburg, MD Associate Scientist I - Process Development Degree in Biology, Life Science or Chemical Engineering field Exp: B.S. with < 1 year of experience |
Catalent Cell & Gene Therapy is looking to recruit a Associate Scientist I, PD to join our growing team in Rockville/Gaithersburg, MD. The Associate Scientist I, PD is actively engaged in downstream and midstream process and product development within a dynamic project team. Displays technical knowledge, initiative and scientific commitment, and makes scientific and technical contributions within the plasmid and AAV downstream purification groups. Participate in the development and implementation of purification processes for multiple projects entering the Catalent Cell and Gene Therapy pipeline. Knowledge/expertise should be practical and focused on lab-related activities. | 7/13/2022 |
| 6469 | Catalent Morrisville, NC Associate Scientist Master’s degree Exp: 0 years |
Under general supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility. Some evaluation, originality or ingenuity is required. Follows established protocols and work plans. May be assisted by laboratory technicians / assistants. | 7/13/2022 |
| 6470 | Catalent Bloomington, IN Associate Scientist Quality Control - Monday to Friday - 11:00P - 7:30A Bachelor’s degree OR Master’s degree in science field Exp: BS: 0-3 years; MS: 0-2 years |
Catalent is seeking an Associate Quality Control Scientist to join our growing team in Bloomington, Indiana. As an Associate Quality Control Scientist, your primary duty will be to provide quality control environmental monitoring, critical utility systems, in-process, finished products, stability, cleaning process, and analytical method validation testing according to SOPs, cGMPs and regulatory guidelines. This is a full time salaried position. The position is Mon-Fri 11:00pm to 7:30am. Catalent is seeking an Associate Quality Control Scientist to join our growing team in Bloomington, Indiana. | 7/13/2022 |
| 6471 | Catalent Bloomington, IN Associate Scientist - QC-M-F 8-5 Bachelor’s degree OR Master’s degree in science field Exp: BS: 0-3 years; MS: 0-2 years |
A quality control (QC) scientist’s primary duty is to provide quality control, in-process, finished products, stability, cleaning process, and analytical method validation testing according to SOPs, cGMPs and regulatory guidelines. Responsibilities include performing and reviewing testing during phases of production, providing technical peer review of testing data, writing/revising technical documents including laboratory procedures, protocols and technical reports, independently utilizing microbiological or analytical instrumentation such as HPLC, GC, UV, ICP-MS, FTIR, TOC, CE, ICE, Karl Fisher, , Plate Reader, performing testing using methodologies such as SDS-PAGE, , IEF, ELISA, PCR, and recognizing atypical/out of specification (OOS) results and perform investigation to determine root cause and implement corrective and preventive actions. | 7/13/2022 |
| 6472 | Catalent Madison, WI Associate Scientist - Process Development, Downstream Bachelor's degree in a STEM discipline Exp: 1-3 years |
The Downstream Process Development team is responsible for the development and implementation of downstream processing methodologies and analytical procedures that can be easily transferred to the cGMP Manufacturing Team. The process characterization function within the Downstream Process Development group will be responsible for the characterization of previously developed or transferred processes heading towards commercial manufacturing. This is a permanent, full time position. It is an hourly role. The shift is Monday-Friday 8a-5p. | 7/13/2022 |
| 6473 | Catalent Madison, WI Associate Scientist, Cell Line Development Bachelors in STEM discipline Exp: 1-3 years |
Monday – Friday, 8:00am – 5:00pm ( weekend work on a rotating basis when needed). The Cell Line Development team is responsible for using the patented GPEx® suite of technologies to create high performance stable cell lines using a non-replicative retrovector system and transfection technologies. This system can be used with any mammalian cell line and many eukaryotic cell lines. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. The Associate Scientist, Cell Line Development, will accurately, timely, and safely perform a variety of laboratory procedures and experimental methods in Cell Line Development that support external client projects and internal technology development work. The Associate Scientist, Cell Line Development will involve performing scientific work involving the creation of cell lines, the creation, production, and purification of retroviruses, and the creation of cell banks, cell culture expansion and production, and cell culture analytical methods | 7/13/2022 |
| 6474 | Cellares South San Francisco, CA Research Associate, Analytical Development (I,II,III) MS/BS in Biological science or related scientific discipline Exp: 0-4 years |
We are seeking an innovative and highly motivated Research Associate in Analytical Development who will contribute significantly to the development of our advanced cell therapy manufacturing platform. The primary focus of this position will be contributing to method development, optimization, and qualification of various analytical methods and providing analytical service support. This is a multidisciplinary role & this individual will interface across many parts of the company (with scientists, researchers, and engineers) to develop the best solutions possible. The successful candidate will be well versed in analytical development. | 7/14/2022 |
| 6475 | Cellectis New York, NY Research Associate I, Gene Editing BS/MS or higher in life science or related discipline. Exp: 1+ years |
We are seeking a highly creative and motivated individual to join us in developing the next generation of cell therapies. The successful applicant will be part of the New York site Innovation team. The candidate will, as part of the team, develop next generation gene and cell engineering approaches using genome editing molecular tools. As part of the Innovation team, the candidate will contribute to the ongoing efforts toward the development of differentiated therapeutic approaches using our gene editing technologies. Candidates should be highly self-motivated with the ability to excel in a fast-moving, goal-oriented environment. | 7/14/2022 |
| 6476 | Cenetron Diagnostics [Versiti] Wauwatosa, WI Research Technologist - Kastrup Bachelors degree from an accredited college or university in biology, chemistry, scientific discipline Exp: One to three years |
Under the direction of the Principal Investigator, performs laboratory assays and complex experiments to elucidate novel research questions. | 7/14/2022 |
| 6477 | Cenetron Diagnostics [Versiti] Milwaukee, WI Laboratory Technologist - Research Bachelor’s degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: one year |
Under supervision by department leadership, this position will support the Hemolysin Assay for organ transplants: Building a donor specific antibody (DSA) model from blood group antigen array data (recognition of RBC glycoproteins) The primary objective is to compare the HLA and blood typing of individuals with their glycan profile using glycan related measures to predict risk. Using glycan-related measures including DNA/RNA analyses, microarrays and antibody testing, a glycan profile can be established and compared to HLA and blood typing results. Small study already conducted, but looking to expand sample size. | 7/14/2022 |
| 6478 | Cenetron Diagnostics [Versiti] Wauwatosa, WI Research Technologist I - Branchford Bachelors degree from an accredited college or university in biology, chemistry, scientific discipline Exp: One to three years |
Under the direction of the Principal Investigator, performs laboratory assays and complex experiments to elucidate novel research questions. | 7/14/2022 |
| 6479 | Cenetron Diagnostics [Versiti] Milwaukee, WI Associate Laboratory Technologist - PNIL Lab- SIGN ON $3500 Bachelor’s degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: Entry-Level |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 7/14/2022 |
| 6480 | ANI Pharmaceuticals Baudette, MN Analytical Development Chemist Analytical Development Chemist Analytical Development Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field or major. Exp: 1-3 years |
This position is responsible for independently performing testing in a pharmaceutical analytical development laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This is a professional position that requires 2-5 years previous experience working in a laboratory performing chormatographic analysis and dissolution testing. | 7/4/2022 |
| 6481 | Ansh Labs Webster, TX SCIENTIST (Monoclonal Lab) Master’s degree in Biology or related area Exp: one or more years |
As a key member of the monoclonal antibody department, this individual will provide critical cell culture, protein engineering, and molecular biology expertise enabling the discovery, design and production of monoclonal antibodies and antigens. | 7/4/2022 |
| 6482 | Ansh Labs Webster, TX SCIENTIST (R&D) Master’s degree in Biological/Chemical Sciences/Biotechnology or related area Exp: 1 year |
As a key member of the R&D department, this individual will provide critical scientific skills to assists in the development and scale up of immunodiagnostic product on various platforms (microtiter based ELISA, magnetic particle based immunoassays, lateral flow assays and micro fludics based immunoassays. | 7/4/2022 |
| 6483 | Aquinnah Pharmaceuticals Cambridge, MA Research Associate Master’s degree in neuroscience, cell biology or related discipline Exp: 1 + years |
The successful candidate should be highly motivated, flexible and enjoy working in a team - based environment with a strong interest in contributing to the discovery of new therapies for the treatment of neurodegenerative disease. This position is laboratory-based and requires strong experimental skills with a background in cell biology, molecular biology, or biochemistry. Under supervision, the candidate will assist in duties including, but not limited to: cell culture maintenance, compound screening, biochemical assays, immunocytochemistry, and analysis using state of the art high-content imaging. Strong communication skills are required including the ability to analyze and report on the results. The candidate will be expected to function efficiently and cooperatively within a team and maintain accurate and clear project records. The ideal candidate will be creative, energetic and motivated. Candidates should have a Bachelor’s or Master’s degree in neuroscience, biology, or related field. Salary will be competitive and commensurate with experience. The successful candidate should be highly motivated, flexible and enjoy working in a team - based environment with a strong interest in contributing to the discovery of new therapies for the treatment of neurodegenerative disease. | 7/6/2022 |
| 6484 | Argonaut Manufacturing Services Carlsbad, CA Manufacturing Technician I (Lyo) Associate’s or Bachelor’s degree, preferred Exp: 1 year |
The purpose of this position is to manufacture lyophilized life science products within the Life Sciences department as well as support other departments and groups as directed. | 7/6/2022 |
| 6485 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. | 7/6/2022 |
| 6486 | Arvinas New Haven, CT Research Associate, Neurodegeneration Biomarkers BS/MS degree in neurobiology or related discipline Exp: 0-2+ years |
As one of the key hires for the company, you will work in close collaboration with leaders and scientists to ensure progression of PROTACs in neurologic disorders. This highly motivated individual will be responsible for the identification and development of translational biomarkers to support our neurology portfolio. Your efforts will be essential for demonstrating target engagement and establishing PK-PD and will play a critical role in lead optimization, development candidate identification and evaluation of pharmacodynamic response in clinical studies. This position will report to a Senior Research Scientist on our Neuroscience team and is located at our headquarters in New Haven, CT.As one of the key hires for the company, you will work in close collaboration with leaders and scientists to ensure progression of PROTACs in neurologic disorders. This highly motivated individual will be responsible for the identification and development of translational biomarkers to support our neurology portfolio. Your efforts will be essential for demonstrating target engagement and establishing PK-PD and will play a critical role in lead optimization, development candidate identification and evaluation of pharmacodynamic response in clinical studies. | 7/6/2022 |
| 6487 | Athenex Buffalo, NY Biologist Minimum of Master of Science degree in Pharmaceutical Sciences or related field Exp: 1 year |
Perform as a subject matter expert in molecular cancer biology and pharmacology in support of Athenex clinical and nonclinical development programs. | 7/6/2022 |
| 6488 | Avance Biosciences Houston, TX Laboratory Associate II Bachelor’s degree in biological sciences Exp: 1 year |
Avance Biosciences Inc., a fast-growing biotechnology CRO, is recruiting several Laboratory Associates in its GLP and/or GMP biological testing departments. This position performs biological tests in accordance with company’s established SOPs to support our customers’ drug discovery, development, and manufacturing activities. | 7/7/2022 |
| 6489 | Avomeen [Element] Ann Arbor, MI Chem II - bioassays BS Exp: 0-2 years |
Element has an opportunity for Chemist II-Bioassays at our Ann Arbor, MI location. The Chemist II will develop analytical methods, perform testing using a variety of technologies and draw conclusions based upon analytical data. Work is performed under the supervision of the lab manager. | 7/7/2022 |
| 6490 | Baxter Cleveland, MS Quality Lab Assoc I B.S. Degree in Science (Chemistry, Chemical Engineering, Physical Chemistry, Biology) Exp: 0-3 Years |
Perform chemical and physical analysis on medical products through all stages of the manufacturing process from incoming raw materials through to product release. Areas include raw materials, initial, in-process and finished products, Stability Program, protocol support, instrumental analysis and instrument calibration/qualifications. Responsibilities also include adherence to regulatory and procedural requirements that govern the operations and products (e.g., Specifications and Cleveland standard operating procedures). | 7/7/2022 |
| 6491 | Baxter Round Lake, IL Quality Lab Associate I Bachelors degree in Chemistry or Science related degree Exp: 6 months + |
The Quality Lab Associate I will be located at the Drug Delivery Chemistry Laboratories, Round Lake, IL. The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. This is a first shift position but will be required to work on weekends to support training of analysts and to support projects and/or production, as required. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 7/7/2022 |
| 6492 | Baxter Round Lake, IL Quality Lab Associate 2nd Shift Bachelors degree in Chemistry or Science related degree Exp: 6 months + |
This is a 2nd Shift 10 Hour Shifts Summary: The Quality Lab Associate I will be located at the Drug Delivery Chemistry Laboratories, Round Lake, IL. The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. This is a second shift position but will be required to work on weekends to support training of analysts and to support projects and/or production, as required. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 7/7/2022 |
| 6493 | Beckton Dickinson San Diego, CA Research Associate II Bachelor’s or Masters degree, in Biology or related scientific discipline. Exp: 1 - 2 years |
The Research Associate II performs routine and complex laboratory tasks and procedures relevant to custom products and services in the Custom Technology Team. The Associate will perform a variety of routine experimental protocols and procedures to fulfill custom manufacturing requirements that include, but are not limited to formulations, experimental design, product testing/analysis, and results reporting. The Associate will work independently within generally defined procedures and practices in selecting methods and techniques for obtaining results. The Associate will observe and comply with safety standards and procedures and assist in general laboratory maintenance. Direction is both verbal and written. | 7/7/2022 |
| 6494 | Beckton Dickinson San Diego, CA R&D Reagent Research Associate BS or BA/ MS degree in Molecular Biology, Chemistry, Biochemistry, or related subject area. Exp: 1 year |
BD is seeking a Reagent Research Associate to work within a team that develops new point-of-care assays for human in vitro diagnostic use. The Reagent Research Associate supports various R&D assay development teams and is principally responsible for the formulation, organization, and quality control of assay raw materials, amplification master mixes, buffers, and consumables. The associate applies good laboratory practice and analytical skills to manage the overall reagent inventory, and material output and works with other team members to resolve technical challenges. Works under the direction of Senior Reagent Scientists or above. | 7/7/2022 |
| 6495 | Beckton Dickinson Lexington, MA Analytical Chemist BSc required; MSc preferred. Exp: 1 year |
BD Lexington is currently seeking a Research Associate who will be involved in many aspects of producing and developing biomaterials, including the analysis, production, isolation, purification and testing of biomaterials within well-defined guidelines. The Research Associate will need to use appropriate analytical tools to characterize and qualify the biomaterials, such as gas chromatography (GC), gel permeation chromatography (GPC) and mechanical testing. S/he will interact with contract testing laboratories to conduct appropriate testing on the materials and may also provide supervision and guidance to junior level technicians. | 7/7/2022 |
| 6496 | Berkeley Lights Emeryville, CA Research Associate, Applications Engineering B.S. in Biology, Chemical Engineering, Bioengineering, Biomedical Engineering, or other multidisciplinary engineering fields Exp: 0-3 years |
The Research Associate/Engineer, Applications is responsible for the coordination and execution of workflows on our BLI platforms to support new product releases. In this new role, you will learn to operate very sophisticated and innovative instruments and support the ongoing development of our platforms. The ideal candidate possesses a strong attention to detail and has demonstrated lab skills experienced in techniques of modern molecular and cell biology or complex biotech instrumentation. You will take ownership for achieving results in biology and technology development programs. | 7/7/2022 |
| 6497 | Bethyl Laboratories [Fortis] San Diego, CA Production Chemist B.A., B.S., or M.Sc. degree Exp: 1+ years |
Work with a team in a fast-paced environment to manufacture products with high reproducibility. Principle duties include: Synthesize, process, and characterize nanoparticles and other manufacturing products using methods such as TFF (Tangential Flow Filtration) in an aseptic environment Preform bioconjugations onto nanoparticle surfaces Meticulously document production into batch records and other forms in accordance with a formal quality systemWork with a team in a fast-paced environment to manufacture products with high reproducibility. Principle duties include: | 7/7/2022 |
| 6498 | Bethyl Laboratories [Fortis] San Diego, CA Research Associate: Lateral Flow B.Sc. OR M.Sc. Exp: BS: 3+ months; MS: 0+ months |
Develop nanoparticle-based lateral flow diagnostics for scientific contracts, grants, and commercial projects. Assemble, run, and optimize lateral flow diagnostic assays to increase sensitivity and minimize non-specific background Preform standard procedures for assay development, including functionalizing nanoparticles, purifying antibodies, striping membranes, running tests, interpreting data, buffer preparation, and running BCA and ELISA assays Operate lateral flow equipment, including the striper, guillotine, laminator, pH probe, nano-drop, and UV-vis Document procedures, observations, and results and independently identify successes and failuresDevelop nanoparticle-based lateral flow diagnostics for scientific contracts, grants, and commercial projects. | 7/7/2022 |
| 6499 | Bethyl Laboratories [Fortis] San Diego, CA Research Associate: Nanoparticle Synthesis Bachelors degree in Chemistry or related field Exp: 6 months + |
Scientific tasks which may include fabrication and characterization of nanoparticles for product inventory and custom orders. Fabricate and characterize standard products with high reproducibility Meticulously document production into lab and electronic notebooks and forms associated with quality system Discuss and analyzes findings with co-workers and managers to collectively select logical tasks to be completed next Independently find solutions to problems by asking questions and reading relevant scientific literatureScientific tasks which may include fabrication and characterization of nanoparticles for product inventory and custom orders. | 7/7/2022 |
| 6500 | BigHat Biosciences San Mateo, CA Research Associate, Mammalian Cell-Based Production Bachelor’s or Master’s degree Exp: 1+ years |
The role: BigHat Biosciences is looking for a motivated and energetic Research Associate with a strong background in mammalian cell-based production to further advance BigHat’s platform for AI-driven antibody discovery and engineering.* | 7/7/2022 |
| 6501 | BioAssay Systems Hayward, CA Research Associate - Assay Development bachelors degree in biochemistry, chemistry, biology, or related field Exp: 1-2 years |
We currently have an exciting opportunity for an enthusiastic research associate to join our growing R&D team. This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers. This is a fantastic opportunity for a motivated recent graduate to be part of a successful and expanding team while learning a number of laboratory skills in a supportive environment. In addition, working on service projects will expose the candidate to multiple other companies and research areas. Moreover, as a small company we offer ample opportunities for professional growth and faster than average promotions. We currently have an exciting opportunity for an enthusiastic research associate to join our growing R&D team. This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers | 7/7/2022 |
| 6502 | BioAssay Systems Hayward, CA Research Associate - Manufacturing college degree in chemistry, biochemistry or biology Exp: 1-2 years |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing, and packaging the finished products. This candidate may also join part time in our R&D team. | 7/8/2022 |
| 6503 | BioFire Diagnostics [Biomerieux] Salt Lake City, UT Research Associate I/II bachelor’s degree with an emphasis in science is preferred. Exp: 0-2 years |
The Research Associate I/II is a technical, hourly position with laboratory responsibilities. The RA I/II works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). The position requires basic proficiency in laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, data analysis, sequence analysis, and a dedication to the mission and goals of the department and bioMerieux. A Research Associate I/II will work collaboratively with other Research Associates, self-direct on routine work with no or minimal instruction and supervision, and will operate with general or detailed instruction and supervision on new procedures and assignments. The Research Associate I/II is a technical, hourly position with laboratory responsibilities. The RA I/II works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). | 7/8/2022 |
| 6504 | BioFire Diagnostics [Biomerieux] San Jose, CA V&V Microbiologist Bachelor’s or Master’s degree in Microbiology or related science discipline Exp: 1 year |
Specific is seeking a Microbiologist with experience in R&D. The role includes experimental research and development to create a cutting-edge In Vitro Diagnostics (IVD) platform. Ideally, you have proven expertise in planning and executing laboratory experiments, data acquisition, and data interpretation. | 7/8/2022 |
| 6505 | BioFire Diagnostics [Biomerieux] San Jose, CA Microbiologist 3:30-Midnight Bachelor’s or Master’s degree in Microbiology or related science discipline. Exp: 1 year |
The Research Associate I/II is a technical hourly position with laboratory responsibilities. The RA I/II works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of FDA and other regulatory submissions. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). The RA I position requires basic laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and BioFire. A Research Associate I may receive general or detailed instruction and supervision on routine work, and detailed instruction and supervision on new procedures and assignments. The Research Associate I/II is a technical hourly position with laboratory responsibilities. The RA I/II works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of FDA and other regulatory submissions. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). | 7/8/2022 |
| 6506 | BioFire Diagnostics [Biomerieux] Salt Lake City, UT Research Associate I/II Bachelor’s degree in a scientific discipline Exp: RAI : 0-2 years |
The Regulatory Affairs and Clinical Affairs departments are responsible for performance assessment and validation of molecular in vitro diagnostic products for global regulatory registrations. The Research Associate I/II is a technical hourly position with laboratory responsibilities. The RA I/II works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of FDA and other regulatory submissions. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). The RA I position requires basic laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and BioFire. A Research Associate I may receive general or detailed instruction and supervision on routine work, and detailed instruction and supervision on new procedures and assignments. The RA II position requires proficiency in laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, data analysis, sequence analysis and a dedication to the mission and goals of the department and BioFire. A Research Associate II will normally self-direct on routine work with no or minimal instruction and supervision, and will operate with general or detailed instruction and supervision on new procedures and assignments. The Regulatory Affairs and Clinical Affairs departments are responsible for performance assessment and validation of molecular in vitro diagnostic products for global regulatory registrations. | 7/8/2022 |
| 6507 | BioFire Diagnostics [Biomerieux] Durham, NC Associate Process Scientist, Biochemist M.S. in Biochemistry or closely related field Exp: 1 year |
As part of the Analytical Production Securitization Industrialization team in the Engineering and Industrialization department, the Associate Process Scientist, Biochemist will perform projects to support the manufacturing of BACT/ALERT® Culture Media products. Within this role the Associate Process Scientist will be required to interface with Manufacturing, Quality Control, Quality Assurance / Validation, R&D, Purchasing, Supply Chain, and other functions as required in order to ensure successful project achievements to facilitate quality production that meets on-time customer demands. | 7/8/2022 |
| 6508 | BioFire Diagnostics [Biomerieux] Saint Louis, MO Lab Technician-Media Lab 3rd Shift Bachelor’s degree in a scientific field required. Biology/Chemistry preferred Exp: one (1) year |
The primary purpose of this position is to prepare complex chemical media and/or sub components, dispensing system setup/verifications, insuring timely delivery of high quality product to Card production, being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 7/8/2022 |
| 6509 | BioLegend [PerkinElmer] San Diego, CA Research Associate I -Diagnostics Bachelor’s degree in a Life Sciences-related field Exp: 1 years |
BioLegend is seeking a highly motivated Product Development Research Associate to join our Diagnostic Product Development Team. This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report.BioLegend is seeking a highly motivated Product Development Research Associate to join our Diagnostic Product Development Team. This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation | 7/8/2022 |
| 6510 | BioLegend [PerkinElmer] Upper Providence, PA Research Specialist - Cell Culture Bachelor’s degree or Master’s degree in Biology, Biotechnology or Biomedical sciences fields Exp: 1 year+ |
We are looking for a highly motivated candidate for the role of Research Specialist to join the growing Synthetic Lethality team. A successful candidate will be responsible for performing standardized, protocol-driven lab-based work (i.e.; maintaining mammalian cell lines, protein isolation, stocking reagents and supplies, etc.). Training will be provided throughout the course of the role, with the goal of the individual to grow into an independent contributor in the laboratory. In this position, the candidate will work within a matrix, collaborative, fast-paced, team environment across diverse biotherapeutic portfolio within the company. | 7/8/2022 |
| 6511 | BioLegend [PerkinElmer] Upper Providence, PA Research Specialist - Cell Culture Bachelor’s degree Required Exp: 6 months |
If you are seeking a meaningful, impactful, and stimulating career, look no further. Job Responsibilities Provide high quality laboratory support to the Synthetic Lethality team. Support multiple ongoing large-scale cell-based projects that are critical to the success and future of the department. Lab work will include mammalian cell culturing, cell proliferation, protein isolation, and viral transduction. Generate and analyze data with the highest Data Integrity standards. Operate and maintain laboratory instrumentation and robotics, including liquid sample handling platforms. Continue technological improvements to increase productivity and cost-efficiency. Data reporting, management, and interactions as appropriate with the teams. Develop organization skills, presentation skills and attention to detail. Interact with senior staff members as necessary. Ensure compliance with all R&D data integrity practices, ethics codes, standards and training, and safety training and practice | 7/8/2022 |
| 6512 | BioLegend [PerkinElmer] San Diego, CA Research Associate I/II - Immunoassay (LEGENDplex) BS in a Biology, Chemistry or other related field Exp: 1 year |
This position is responsible for supporting immunoassay products development and manufacturing in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working with an experienced scientist on testing new hybridoma clones, qualifying the raw materials used for immunoassay products manufacturing and new immunoassay product development and launching. These immunoassay products may allow simultaneously detection of up to 13 important biomarkers for inflammatory diseases, stem cells, cancer, cardiovascular disease or neuron degenerative diseases, and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experiences in growing business in a fast-pace biotech industrial environment. He or she will be able to manage the assigned function and tasks with great communication skills in a timely manner with independence after appropriate training. | 7/8/2022 |
| 6513 | BioLegend [PerkinElmer] Cambridge, MA Research Specialist - Cell Culture, Synthetic Lethality Bachelor’s degree Master’s degree in Biology, Biotechnology or Biomedical sciences fields Exp: 1 year |
We are looking for a highly motivated candidate for the role of Research Specialist to join the growing Synthetic Lethality team. A successful candidate will be responsible for performing standardized, protocol-driven lab-based work (i.e.; maintaining mammalian cell lines, protein isolation, stocking reagents and supplies, etc.). Training will be provided throughout the course of the role, with the goal of the individual to grow into an independent contributor in the laboratory. In this position, the candidate will work within a matrix, collaborative, fast-paced, team environment across diverse biotherapeutic portfolio within the company. | 7/8/2022 |
| 6514 | BioLegend [PerkinElmer] San Diego, CA Research Associate I - Process Development - Antibody Conjugation Bachelor’s Degree in Biology, Biochemistry, Chemistry, or related Science. Exp: 6 months |
The position is an important member of a team to pre-screen and optimize conditions for new product launch and for product transfer to manufacturing. The position works with antibodies and reagents for research areas including immunology, neuroscience, stem cells, and cell biology. This is a great opportunity to enhance your knowledge in a highly competitive biotechnology industry. BioLegend is a fast growing company and an industry leader who is committed the effort to provide top line quality products to our customers and the best tools for scientific community. This position is lab based and will work independently in a team setting to perform all essential functions that related to small scale antibody production, conjugation, and purification. It requires the ability to follow SOPs, complete batch records, and finish assignments in a timely manner. This position will also perform troubleshooting, and also responsible for assisting the supervisor with laboratory operations and completing production requirements before due dates. | 7/8/2022 |
| 6515 | Bio-Rad Hercules, CA Research Associate I Recent college graduate with a BS degree in biology/chemistry/biotechnology/biomaterials/biochemistry/biomedical engineering or other related field in Exp: Entry-Level |
Bio-Rad Laboratories is seeking a highly motivated individual to join the Chemistry R&D team as a Research Associate. The candidate will be involved in the research and development of antibody conjugate and affinity chromatography products and will generate data in support of product development, applications, and customer assistance. The position will require interfacing with R&D scientists and engineers, marketing and manufacturing personnel, and external collaborators. | 7/8/2022 |
| 6516 | Bio-Rad Pleasanton, CA Research Associate I BS in Molecular Biology or Biochemistry Exp: 0-2 years |
We are looking for a Research Associate I to join our Product Development team at Bio-Rad – Digital Biology Group. Responsibilities Perform NGS library preparation and conduct key experiments to optimize formulations and workflow. Assist in the development of product specifications and quality metrics to deliver optimum product performance. Execute Verification/Validations studies and report findings. Assist in data analysis and documentation. Maintain fresh cell lines and manage frozen cells supply. Train and support transfer/operations teams in preparation for product launches. | 7/8/2022 |
| 6517 | Bio-Rad Hercules, CA Research Associate I (Temporary) Recent college graduate with a BS degree in chemistry/biotechnology/material science/polymer science/chemical engineering or other related field in li Exp: Entry-Level |
Bio-Rad Laboratories is seeking a highly motivated individual to join the Chemistry R&D team as a casual research associate. The candidate will be involved in the research, synthesis and characterization of small molecules, polymers and nano-materials. | 7/8/2022 |
| 6518 | Bio-Rad Woodinville, WA Production Chemist I Bachelor’s degree in a life science or related field. Exp: 0-3 years |
Manufacturing activities for BioPlex2200 to support commercialization and development activities. Areas of responsibility could include bead coupling, conjugation, calibrator and control manufacturing, or other component manufacturing. | 7/8/2022 |
| 6519 | Bio-Rad Woodinville, WA Quality Control Specialist I BS/BA degree in the physical sciences required Exp: 0-2 years |
The QC Specialist position involves production of commercial products with an emphasis on supporting raw material and in-process commercial testing. Specific duties include performing BioPlex QC assays and performing special projects. Testing will include BioPlex testing for assay component raw materials, bulks, fills, raw materials and finished kits tested according to FDA/ISO regulated manufacturing and per document methods employing Good Laboratory Practices. | 7/8/2022 |
| 6520 | Inotiv St Louis, MO Research Technician Biological sciences degree,Registered Veterinary Technician (ALAT, LAT, or LATG) Exp: 1-3 years |
Accurately perform basic laboratory calculations and measurements Perform various routine techniques including animal identification, clinical observations, restraint, animal randomization, test article administration (including but not limited to gavage, dermal applications, IV, IP, and subQ), and specimen collection Ability to successfully perform all study activities in a high-paced environment working with team members in a time-sensitive manner. Competency in the use of relevant computer systems including electronic in-life data collection systems. Clearly and accurately document study activities following Inotiv requirements for written and electronic data recording and data integrity. Compliance with applicable USDA regulations, Animal Welfare Act, facility Animal Care and Use Committee requirements, and the Guide for Care and Use of Laboratory Animals. | 6/27/2022 |
| 6521 | Inotiv Boulder, CO IHC Research Associate I Associates or bachelor’s degree - preferably in Biology, Chemistry, or a related science Exp: 1+ years |
Under the direct supervision of the IHC Manager, performs immunohistochemical (IHC), immunofluorescent (IF) and in situ Hybridization (ISH) staining and testing in accordance with established standards and procedures using an automated staining platform. Maintains accurate and detailed records of work performed and results generated. Under the supervision of IHC management and IHC Scientists helps assess staining results for QC purposes. Is responsible for organization and inventory of lab supplies and reagents, routine cleaning and maintenance of lab equipment, and general lab cleanliness and upkeep. Strong team coordination, effective communication, high attention to detail and a commitment to high-quality data are critical to achieving success on the IHC team. | 6/27/2022 |
| 6522 | Inotiv Rockville, MD Associate Scientist - Biotherapeutics BSc or MSc in Immunology, molecular biology, bioanalytical chemistry, drug metabolism, pharmacokinetics, or related science Exp: 1-3 years |
The associate scientists should have knowledge and experience in ligand binding assay techniques, e.g., ELISA, MSD, Luminex, cell-based assays for PK and Immunogenicity determinations, or knowledge of PCR, DNA, RNA analysis, as well as flow cytometry. Due to the different techniques involved, some associate scientists would need essential experience in PCR, DNA, RNA, and flow cytometry analysis with a working knowledge of ligand binding assay techniques, e.g., ELISA (HELISA, etc.), MSD, Luminex, cell-based assays for PK and Immunogenicity determinations and LC-MS/MS. Depending on their experience and capabilities they will be placed in the different sections. The associate scientists of the Biotherapeutics laboratory will perform analysis of samples generated in the GLP/GCLP laboratory for preclinical samples according to the applicable FDA/EMA Guidelines. The associate scientists will thrive in a collaborative and welcoming environment that values a culture of empowerment, transparency, innovation, agility, professional growth, and credibility providing them the opportunity for promotion to scientists. | 6/27/2022 |
| 6523 | Inotiv Gaithersburg, MD Associate Scientist I Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 1+ years’ |
Perform a wide variety of in vitro assays or tests required to characterize product or material safety. Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations. Maintain an understanding of technological principles and applications of the organization’s services. Receive instructions on new assignments from the laboratory manager or designee and study directors. Conduct pre-designed assays using basic laboratory techniques and skills. Independently conduct assigned test procedures within constraints of lab scheduling Advise lab manager of factors that may affect the quality and usefulness of data Maintain sterile and good tissue culture techniques. Use and maintain scientific equipment, instrumentation and computer systems. Attend, pre-planning, or operational team meetings as needed. Assist or perform other job duties as assigned. | 6/27/2022 |
| 6524 | Inotiv Gaithersburg, MD Associate Scientist I (In Vitro Cytogenetics) Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 1+ years |
Position Responsibilities: Perform a wide variety of in vitro assays or tests required to characterize product or material safety Maintain sterile and good cell/tissue culture techniques Prepare study reagents in accordance with SOPs and study instructions Use and maintain scientific equipment, instrumentation and computer systems Conduct pre-designed assays using basic laboratory techniques and skills Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations Perform peer review of data and lab support records Keep the next level manager and Study Director informed of study status, technical problems and other issues which impact the lab/study Address quality audit findings and generate deviations using the quality system, as needed Receive instructions on new assignments from the laboratory manager or designee and study directors | 6/27/2022 |
| 6525 | Uptake Medical [Crown] Johnson City, TN Associate Scientist Bachelor’s degree in Chemistry or other related discipline. Exp: 0-2 years |
The Associate Research Scientist is responsible for assisting the Research Scientist and the R&D department in the development of new products from concept to commercialization to support company growth. | 6/27/2022 |
| 6526 | Uptake Medical [Crown] Johnson City, TN Chemist Bachelors’ Degree in Chemistry from an accredited college or university Exp: 0-3 years’ |
Responsible for performing testing of raw materials and components, finished products, and stability samples as well as in process tests. In addition, the Chemist is also responsible for assisting in the maintenance and calibration of analytical instruments, preparation of standard and sample solutions and maintenance of associated records. | 6/27/2022 |
| 6527 | Wugen St Louis, MO/ San Diego, CA, MO Associate Scientist: In vitro BS/MS degree in biology, engineering or related Exp: 1+ years |
Wugen Inc. is seeking exceptional and highly motivated candidates to join our growing R&D team in St Louis and San Diego. This scientist will work closely with fellow synthetic biology scientists to develop and evaluate the activity and efficacy of novel candidate cellular therapeutics. This candidate will be responsible for the execution and analysis of preclinical studies and will play a vital role in the translation of our novel cell therapies to the clinic. The compensation package will be competitive and commensurate with qualifications and experience. | 6/27/2022 |
| 6528 | Wugen St Louis, MO/ San Diego, CA, MO Associate Scientist: In vivo BS/MS in immunology, biology, pharmacology, or related scientific discipline Exp: 1+ years |
Wugen Inc. is seeking exceptional and highly motivated candidates to join our growing R&D team in St. Louis and San Diego. This candidate will be responsible for establishing and performing in vivo testing to guide the selection and development of cellular therapies using mouse models of cancer. The compensation package will be competitive and commensurate with qualifications and experience. | 6/27/2022 |
| 6529 | 1910Genetics Boston, MA Research Associate - Biology B.S. or M.S. in Biology, Cell Biology, Molecular Biology, Biochemistry, Pharmacology, or equivalent Exp: 0 – 3 years |
Executing high throughput screening (HTS) assays in strict accordance with the NIH NCATS Assay Guidance Manual Developing and validating HTS biochemical assays for characterizing the activity and selectivity of potential drug candidates Developing and validating HTS cell-based assays for characterizing the activity, selectivity, and cellular permeability of potential drug candidates | 6/28/2022 |
| 6530 | Abbott San Diego, CA Research Associate I BA/BS in Biology, Chemistry or related field Exp: One year or more |
We have an exciting opportunity for a Research Associate I within our Abbott Rapid Diagnostics business. The position of Research Associate I is within our Cardiometabolic Research and Development Business Unit located in San Diego, CA. Under general supervision, the scope of this position is responsible for assisting senior scientific staff in carrying out moderately complex research assignments involving a variety of laboratory methods, equipment and procedures. | 6/28/2022 |
| 6531 | Abbott San Diego, CA Research Associate I, Assay Development B.S. in biology, biochemistry, chemistry, microbiology, or a related field Exp: Entry Level |
We have an exciting opportunity for an Innovative Research Associate – Assay Development within our Abbott Rapid Diagnostics business located at Carlsbad, CA. In this role, you will help expand test content on the ID NOW™ platform by designing, screening and optimizing novel assays as well as engaging in research activities focused on expanding the capabilities of the core technology. Now is an exciting time to join! | 6/28/2022 |
| 6532 | AbbVie Worcester, MA Associate Scientist, Cellular and Molecular Biology BS or MS in Biochemistry, Molecular Biology, Cell Biology, or a related discipline Exp: 0-3+ (BS) or 0+ (MS) years |
AbbVie Immunology is dedicated to identifying break-through therapies for inflammatory and auto-immune diseases that will have a remarkable impact on patients’ lives. The Molecular and Cellular Pharmacology group is seeking an Associate Scientist responsible for conducting in vitro studies on the characterization of drug candidate molecules and the validation of drug targets. | 6/28/2022 |
| 6533 | AbbVie Worcester, MA Associate Scientist, Molecular Biology B.S. in Biochemistry, Molecular Biology, or equivalent discipline; or MS in equivalent field Exp: BS: 0-3+ years ; MS: 0+ years |
As a member of the Multi-Specific Biologics Group, you will be responsible for the cloning, production, and analysis of novel multi-specific antibodies. A successful candidate will have experience in multiple facets of molecular biology. Proficiency in protein expression, purification and characterization is desired. Experience with plate-based assays is nice to have. The candidate must have a proven track record of delivering high quality experimental data. Experience with automated liquid handling and tools for data capture would also be desirable. In addition, the candidate must be able to demonstrate individual contributions to projects and to possess strong interpersonal skills. The scientist will be expected to represent the Multi-specific Biologics group and present their data in project team meetings. | 6/28/2022 |
| 6534 | Abveris Quincy, MA Research Associate: Protein Analytics Bachelor’s or Master’s degree in a scientific discipline required (Biology, Biochemistry, Biochemical Engineering) Exp: 1-3 years |
We are seeking a motivated individual to join our team and expand our bioanalytical department. Using state-of-the art technologies and workflows, this Research Associate would work with the Protein Analytics team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 6/28/2022 |
| 6535 | Abveris Quincy, MA Research Associate: Tissue Culture Bachelor’s degree in a scientific discipline required Exp: 1+ years |
We are currently seeking a Research Associate for our cell culture group to support hybridoma and recombinant expression antibody discovery platforms. In this lab-based role, attention to detail, ability to multitask and working both independently and in group settings will be critical for success. You will work directly with the cell culture group for a range of projects to produce, select and scale hybridoma cell lines, while also supporting recombinant expression platforms in a rapidly growing environment that is always eager to optimize processes. A Bachelor’s degree in a scientific discipline is required and prior laboratory experience in cell culture and aseptic technique is strongly preferred. | 6/28/2022 |
| 6536 | Abveris Quincy, MA Research Associate: Molecular Biology Degree in Biology or other related discipline Exp: 1+ years |
We are seeking a motivated individual to join our Molecular Biology team and contribute to cloning, antibody sequencing, single B cell discovery and additional molecular biology workflows. The role will be lab-based and integral to expanding our molecular biology capabilities as our company continues its rapid growth trajectory and passion for integrating state-of-the-art technology and custom antibody discovery techniques. The ideal candidate will have previous hands-on experience with immune cell sample processing, PCR amplification and cloning techniques. Technical proficiency in a combination of the following is also desired: Next Generation Sequencing (NGS) workflows, antibody sequence analysis and high throughput downstream molecular biology techniques required for various cloning methods and subsequent recombinant expression. Meticulous attention to detail, proficient reasoning and problem-solving skills are cornerstones for a successful candidate. | 6/28/2022 |
| 6537 | Accent Therapeutics Lexington, MA Research Associate/Senior Researcg Associate, Biology BS/MS in Biology or related field Exp: 1-2 years |
As a key member of the Biology team, this Research Associate or Senior Research Associate will join a dynamic, enthusiastic, highly interdisciplinary, and collaborative team to elucidate the role of epitranscriptomics in human disease, and progress the Accent pipeline. | 6/28/2022 |
| 6538 | Adicet Bio Redwood City, CA Manufacturing Associate 2 - Cell Therapy Bachelor’s degree in a biological science, engineering or related science discipline Exp: 1-3 years |
We are seeking a highly motivated and experienced individual with a strong background in cell process development/manufacturing. The Manufacturing Associate 2 will report to the Director of Manufacturing. In this role you will support the daily manufacturing operations of allogeneic CAR T cell therapies, assist with troubleshooting complex and non-routine equipment events, initiate and support deviations, and author SOPs. You will implement Good Manufacturing Practices and best practices to streamline manufacturing operations. You will demonstrate expertise and breadth of knowledge in executing processes across a variety of production activities such as cell processing, aseptic behavior, monitoring equipment and processes, product sampling, and conducting routine sanitization tasks to maintain facility and equipment. You will read and follow defined SOPs and policies, work independently on basic manufacturing tasks, identify, and communicate non-routine events, and review more complex decisions with your direct supervisor. | 6/29/2022 |
| 6539 | Adicet Bio Redwood City, CA Manufacturing Associate 2 - Viral Vector Bachelor’s degree in a biological science, engineering or related science discipline Exp: 1 – 3 years |
We are seeking a highly motivated and experienced individual with a strong background in viral vector development/manufacturing. The Manufacturing Associate 2 will report to the Director of Manufacturing. In this role you will support the daily manufacturing operations of allogeneic CAR T cell therapies, assist with troubleshooting complex and non-routine equipment events, initiate and assist with deviations, review batch records, and author SOPs. You will implement Good Manufacturing Practices and best practices to streamline manufacturing operations. You will demonstrate expertise and breadth of knowledge in executing processes across a variety of production activities such as cell processing/purification, aseptic behavior, monitoring equipment and processes, product sampling, and conducting routine sanitization tasks to maintain facility and equipment. You will read and follow defined SOPs and policies, work independently on basic manufacturing tasks, identify, and communicate non-routine events, and review more complex decisions with your direct supervisor. | 6/29/2022 |
| 6540 | Adicet Bio Redwood City, CA QC Associate, Microbiology BS in biological sciences or a related field Exp: 0-5 years |
This position offers the opportunity to learn and develop in the field of QC Microbiology in support of cutting-edge cell therapy manufacturing. We are seeking a highly motivated candidate with a background in microbiology and cleanroom environment to join Adicet as a QC Microbiology Associate. The successful candidate will work as a part of Technical Operations team, to facilitate the production of viral vectors and cellular therapy products. | 6/29/2022 |
| 6541 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences Exp: BS: 1-3 years; MS: 1+ years |
Preparing solutions and reagents for performing assays on the bench Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance Perform Operational Qualification and Performance Qualification on Next Generation Sequencers | 6/29/2022 |
| 6542 | Admera Health South Plainfield, NJ Associate Scientist I Project Management Team B.S./M.S. in Biological Sciences Exp: 1+ years |
Relay standard information on next generation sequencing applications to customers Standard communication with prospective, current, and past customers Co-coordinating multiple genomic projects with excellent documentation skills and communication to customers Collaborate within group to streamline incoming, ongoing, completed projects – minimally cross-departmental Learn relevant next generation sequencing materials for RUO applications Comply with all CLIA/CAP regulations | 6/29/2022 |
| 6543 | Allakos San Carlos, CA Research Associate I/ Research Associate II, Bioassay and Process Analytics Degree (BS, MS) in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific field. Exp: 0-1 year |
The company is seeking to recruit a Research Associate to join our expanding team in the group of Analytical Development and Process Analytics. The scope of the position and requirements are described below. The successful candidate will play a key role in supporting our ongoing product development. Responsibilities includes sample analysis using analytical methods which include, but are not limited to, SEC (size exclusion chromatography), CEX (cation exchange), CE (capillary electrophoresis) and plate-based assays such as residual DNA by qPCR and ELISA. The candidate will have the opportunity to learn a broad range of analytical methods from molecular characterization to functional assessment. The candidate is expected to plan, execute, analyze and document the laboratory studies. The focus of the position is to work in the process analytics laboratory. | 6/29/2022 |
| 6544 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, In Vivo Sciences BS in Biology or related field Exp: 1-3 years |
An Associate Scientist II is responsible for organizing, conducting, and reporting non-GLP rodent toxicology, investigative, and pharmacokinetics/toxicokinetics (PK/TK) studies that support drug discovery and development. | 6/29/2022 |
| 6545 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, in Vivo Pharmacology BS or MS in Animal/Veterinary Sciences, Cell/Molecular Biology, Biochemistry, or related field Exp: 0-3 years |
We are currently seeking a highly motivated Associate Scientist II with experience in small-animal pharmacology to join our dynamic, fast-paced and interdisciplinary team. Our mission is to drive the pre-clinical evaluation of siRNA-based therapeutics. The role requires a background in biological sciences and be technically skilled in in vivo preclinical research as well as molecular techniques. The candidate must have strong interpersonal skills, the capacity to multi-task, and the ability to learn and master new techniques in various fields, including CNS and ocular. We particularly seek someone who is detail-oriented and who will flourish in a goal-driven team environment under tight deadlines. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 6/29/2022 |
| 6546 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, RNAi Discovery BS in a biological science Exp: 1 year |
We are currently seeking a passionate and experienced Associate Scientist II with background in in vitro screening to join our dynamic, fast-paced and interdisciplinary lead development team. Our mission is to advance novel RNAi therapeutic programs from target discovery through lead candidate selection. The successful candidate will be technically skilled in biochemistry or cell biology, and bring a rigorous, analytical approach to research. | 6/29/2022 |
| 6547 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 6/29/2022 |
| 6548 | Alveo Technologies Alameda, CA Laboratory Technician (Contract) Technical degree in Biology, Chemistry, Molecular Biology, or equivalent technical field Exp: 1+ years |
Alveo Technologies is looking for a Laboratory Technician with experience supporting laboratory formulation and manufacturing. Our candidate will be responsible for contributing to the growth of the company by manufacturing novel diagnostic consumables and/or analyzers in a production environment. This will be an Entry-Mid level position responsible for supporting the Bulk Buffer, Reagent, and Cartridge production laboratories by following good documentation practices (cGDP) and relevant manufacturing process instructions (MPI). Responsibilities of this role include micropipetting, following standard operating procedures, using laboratory equipment, and mechanical assembly to meet all standards for safety, quality and efficiency in a clean room environment. This position has direct accountability for assembly quality and throughput. This individual will support the development of systems that drive and support continuous improvement and high levels of performance through effective utilization, equipment, facilities, tools, direct and indirect materials. | 6/29/2022 |
| 6549 | Norwich Pharmaceuticals [Alvogen] Norwich, NY Process Engineer I BS degree or higher in related field Exp: 0-3 years |
The Process Engineer I perform activities surrounding manufacturing process scale-up, technology transfers (internal and external), process validation and process optimization. | 6/29/2022 |
| 6550 | Amarex Clinical Research Ypsilanti, MI Technician II Labs, Engineering BS degree in an engineering or scientific discipline. Exp: One year |
As a Technician II for Engineering Plastics, you will be responsible for conducting testing of equipment, products, and materials for conformance to NSF, ASTM, and other standards. You will work a part of an exciting large team responsible for various testing procedures and can learn and grow in new lab environments (i.e., plumbing, soldering, etc.) | 6/29/2022 |
| 6551 | Amarex Clinical Research Ann Arbor, MI Lab Technician , Exposures Lab AAS/BS degree is a plus Exp: 1 to 5 years |
Technician II - Exposures Lab needed with good basic lab skills and an aptitude for understanding and using machines or tools. Experience with plumbing equipment a plus. Great entry level position to learn about product certification work and to start a career in the sciences for a mission driven company. | 6/29/2022 |
| 6552 | AmbioPharm North Augusta, SC QC Chemist II Masters Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Hands on experience with HPLC, GC, IC, KF and other routine analytical equipment such as pH meter and balance. Perform quality control routine testing for raw material/ Intermediate/ Release / Stability testing Perform Method development and method validation execution, including writing protocols and reports. Must be proficient. Responsible for reviewing analytical laboratory raw data and electronic records. Participate in out of specification (OOS) investigations, as well as other deviations and writing investigation reports. | 6/29/2022 |
| 6553 | AmbioPharm North Augusta, SC QC Chemist I Bachelor’s Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Perform and review QC release testing. Support routine analytical testing using GC, KF, and HPLC. Assist the QC/QA group with writing and editing of SOPs and STPs Support analytical method development. Perform method transfer and validation activities. Perform OQ/PQ for the Quality Control Equipment. Other duties as assigned. | 6/29/2022 |
| 6554 | AmbioPharm North Augusta, SC QA Associate I Bachelors Science Degree is required. (Chemistry, Biology, or other Life Science degree) Exp: 0-1 year |
Review and release of raw materials. Ensuring that all materials are reviewed and released within the required time frame. Request deviations are needed. Track and disposition materials past re-evaluation dates. Review and track all temperature chart recorders. Request deviations as needed. Review and disposition cleaning verification batch records and testing packages. Perform room and equipment clearances per procedure following cleaning conducted by production. Maintain a full understanding of all AmbioPharm SOPs and policies along with all cGMP, CFR, ICH guidances that are applicable to the manufacturing of APIs. Issues re-packaging paperwork and performs review and approval when returned. Tracks the documentation through the process. Issues labels as requested. Perform weekly housekeeping tour | 6/29/2022 |
| 6555 | Ambry Genetics Aliso Viejo, CA Research Associate II BS degree in a life sciences field: Biology, Molecular Biology, Biochemistry or related field. Exp: 0-2 years |
Research Associate II is responsible for assisting senior R&D and Clinical Validation staffs with minimal supervision to design, develop, and validate clinical diagnostic assays spanning a wide range of Next-Generation sequencing and microarray technologies. | 6/29/2022 |
| 6556 | Ambys Medicines South San Francisco, CA Research Associate/Senior Research Associate/Associate Scientist, Bioanalytical and Assay Development MS in Biological Sciences Exp: 0-4+ years |
We are seeking an enthusiastic and motivated Research Associate/Senior Research Associate/Associate Scientist to make impactful contributions to the Bioanalytical and Assay Development group. The ideal candidate will incorporate their diverse skillset to develop cell-based assays to characterize Ambys’ hepatocyte cell therapy product and to support non-clinical IND-enabling studies. | 6/29/2022 |
| 6557 | Amunix Pharmaceuticals South San Francisco, CA Lab Technician S. in Chemistry or Biology or similar scientific discipline Exp: 1-2 years |
The Lab Tech is responsible for supporting routine operations of the Fermentation and Purification Labs and completing routine laboratory procedures under the direction of the BioProcess Development and Manufacturing Lead. | 6/29/2022 |
| 6558 | Amunix Pharmaceuticals South San Francisco, CA Research Associate, Purification Bachelor’s degree in protein chemistry, biochemistry, pharmaceutical sciences, or similar Exp: 1 year |
The Research Associate will join the Protein Purification and Process Development function and contribute to the performance of Amunix’s established purification processes, development, and optimization for new molecules, and support project-specific purification development strategies. This position heavily supports Amunix’s internal production and R&D efforts, and it interfaces internally with Molecular Biology, Fermentation Operations, and Analytical Chemistry as well as externally with partners both domestic and abroad. Initiative, ingenuity, flexibility, communication, and work ethic are paramount in this role. | 6/29/2022 |
| 6559 | AnaSpec Fremont, CA Research Associate-Assay Kits BS in Biochemistry, Chemistry, Cell Biology or related discipline Exp: 0-3 years |
Use your expertise to make a difference in disease research and drug discovery around the world. We manufacture custom and catalog products that are employed by scientists from biopharmaceutical corporations and top-tier academic institutions, to actively study such diseases as Alzheimer’s disease, Multiple Sclerosis, Cancer, Cardiovascular disease, Diabetes, COVID and so much more. | 6/29/2022 |
| 6560 | Noble Life Sciences Woodbine, MD Animal Lab Tech Bachelor's degree in a scientific discipline Exp: 1 year |
The Animal Lab Tech – is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Vivarium Manager. | 6/13/2022 |
| 6561 | Noble Life Sciences Woodbine, MD Study Coordinator Bachelor's degree in a scientific discipline Exp: 1 year |
The Study Coordinator – is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Study Directors. | 6/13/2022 |
| 6562 | Noveome Biotherapeutics Pittsburgh, PA Biological Manufacturing Associate I ASSOCIATE’S OR BACHELOR’S DEGREE - BIOLOGY, MICROBIOLOGY, BIOTECHNOLOGY Exp: 0+ YEARS’ |
The Biological Manufacturing Associate I performs cell culture, product collection and filtration for use in finished product manufacturing. This position has responsibility for facility and equipment cleaning and operations. This position will spend a vast amount of time learning specific techniques and processes in order to function in this position. This position will adhere to GMP guidelines and processes are compliant with FDA CFR part 210-211. | 6/13/2022 |
| 6563 | Oakwood Labs Solon, OH Quality Control Chemist Bachelor's degree in Chemistry, Biochemistry, Biology, or related field Exp: 1 - 4 years |
We are currently seeking individuals to: Perform stability studies Perform raw material, in-process product, and final product release testing Assess data to determine if the material tested meets specifications Participate in investigational testing and write reports Execute mathematical calculations as outlined in test methods | 6/13/2022 |
| 6564 | Oakwood Labs Solon, OH Chemist Bachelor’s degree in chemistry, biology, or related discipline Exp: Entry Level |
Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development. | 6/13/2022 |
| 6565 | Oakwood Labs Solon, OH Chemical Engineer/ Biomedical Engineer Bachelor of Science, Masters, or PhD Degree in Biomedical or Chemical Engineering, or Chemistry or closely related science field with chemistry and ma Exp: Entry Level |
This is an excellent entry-level opportunity for those interested in working at a technology-based pharmaceutical company. The successful incumbents will work in our product development function and: Perform pre-formulation laboratory experiments and studies Perform process scale-up from laboratory to pilot laboratory Perform process scale-up from pilot laboratory to manufacturing facility Work on technology transfer activities. | 6/13/2022 |
| 6566 | Patheon Sunnyvale, CA Formulation Technician II Bachelor Degree in Chemistry/ or equivalent required. Exp: 1+ years |
This position is responsible for the production of various columns and related consumables and works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. Exercises judgment within defined procedures and practices to determine appropriate action. Under general supervision, reads bills of material, discrete jobs and production procedures then performs assembly, packing, equilibration; testing using various ion chromatography equipment, and embalming of columns and related consumables. This colleague follows written and verbal instructions using common laboratory equipment | 6/13/2022 |
| 6567 | Patheon Bend, OR Formulation Technician II Bachelor’s degree in physical science, chemistry, chemical science, material science, engineering, or related field preferred Exp: One year |
Provide technical and manufacturing support to the Formulation and Process Development (FPD) Engineers and/or Scientists in the production of pharmaceutical Spray Dried Intermediates (SDI) along with Solid Dosage Forms (tablets, capsules, sachets). | 6/15/2022 |
| 6568 | Patheon Alachua, FL Formulation Technician II Bachelor’s Degree in related field Exp: 0+ years |
The Associate II position will support cGMP manufacturing activities to ensure that Thermo Fisher Scientific Viral Vector Services provides clients with gene therapy products for pre-clinical and clinical use. This position will perform hands on cGMP production of recombinant protein and viral vectors under the supervision of the Downstream Manufacturing Leadership. | 6/15/2022 |
| 6569 | Patheon Frederick, MD Scientist I, Formulation Bachelor’s degree in Biology preferred. Exp: 0-2 years |
The Advanced Cell Systems Production team at Thermo Fisher Scientific is responsible for manufacturing various Primary tissue derived products including cells, RNA and subcellular fractions along with reagents and for a variety of biological applications. Our team is dynamic and fast paced, relying on teamwork, multitasking and communication within the team and the larger organization. We are seeking an energetic individual with strong communication, technical and operational skills to join our team. The candidate will follow SOPs and work in compliance with EH&S, GLP, and any other required manufacturing or company systems (e.g. E1, Agile, Trackwise, etc.). This position will be responsible for supporting the team in achieving daily production schedules and product quality goals. | 6/15/2022 |
| 6570 | Patheon Frederick, MD Scientist I, Cell Biology R&D Bachelor’s degree in Biology, Bioengineering, Biochemistry, or a related subject area Exp: 1-3 years |
You will work as a part of Advanced Cell Models R&D to support ongoing projects within the Thermo Fisher product commercialization process under the Gibco™ brand. You must have experience with cell culture, either immortalized cell lines or primary cells. The candidate should also have familiarity with downstream analyses, including the evaluation of cells via microscopy, Western blot, flow cytometry, or similar techniques. An innovative and curious mentality, attention to detail, and ability to multitask while maintaining a focus on critical projects are critical. | 6/15/2022 |
| 6571 | Patheon Carlsbad, CA Scientist I, Cell Biology Bachelor’s degree in Life Sciences or Chemical/Biological Engineering (or closely related field) Exp: one year |
As a Scientist I in the Analytical Sciences Laboratory, you will support the development, qualification and execution of cell-based, nucleic acid-based, protein-based and chemistry-based assays that support quality control of cell and gene therapy products and mRNA vaccines under development and manufacturing. | 6/15/2022 |
| 6572 | Phase Genomics Seattle, WA Software Engineer B.S. or B.A. in computer science, software engineering, bioinformatics, or other technical fields with a programming bent. Exp: 1-4 years’ |
Phase Genomics is seeking smart, talented, motivated web engineers to design and build the infrastructure and user interfaces that host our revolutionary genomic analysis tools. Our engineers work across a wide range of technologies, from the front end to the back end, designing everything from database-driven web applications to web-based user collaboration tools to massively parallel data analysis systems. We are a cloud-native company built on AWS, taking advantage of services like EC2, S3, DynamoDB, RDS, SageMaker, Lambda, and more. We leverage additional state-of-the-art tools such as Django, Terraform, and Ansible, and develop primarily in Python and Javascript, though we will use whatever language is the right tool for the job. | 6/15/2022 |
| 6573 | Karl Storz Endoscopy-America Goleta, CA Design Verification Test Engineer I - Contract Staff BS degree in Electrical Engineering, Mechanical Engineering, Software Engineering, Computer Engineering, Biomedical Engineering, or related field. Exp: 0-2 years’ |
Join a dynamic team of engineers designing endoscopic cameras and imaging systems for one of the world-leading medical device manufacturers of surgical equipment – KARL STORZ! As a member of the Design Verification team in Goleta, CA, the Test Engineer I position holds key responsibilities for ensuring KARL STORZ’s line of video imaging systems continue to maintain their reputation among surgeons and medical staff for delivering world-class quality. | 6/15/2022 |
| 6574 | Karl Storz Endoscopy-America Goleta, CA Design Verification Test Engineer II - Contract Staff MS degree in Electrical Engineering, Mechanical Engineering, Software Engineering, Computer Engineering, Biomedical Engineering, or related field Exp: 0-3 years’ |
As a member of the Design Verification team in Goleta, CA, the Test Engineer II position holds key responsibilities for ensuring KARL STORZ’s line of video imaging systems continue to maintain their reputation among surgeons and medical staff for delivering world-class quality. The role responsibilities include the following test engineering functions: • Leading verification efforts, which includes planning verification schedules, communicating with project team members, and directing test tasks for other Test Engineers. • Testing prototypes to verify they meet quality prior to release to production. • Characterizing the mechanical, electrical, reliability, and imaging performance of existing products and functional models. • Documenting results for internal and external quality and regulatory processes. • Designing tests to meet new product mechanical, electrical, and imaging performance measurement challenges. • Automating tests using Matlab and a C#-based scripting framework. • Troubleshooting product issues related to product quality, manufacturability, reliability, efficacy and regulatory compliance. | 6/15/2022 |
| 6575 | Karl Storz Endoscopy-America Goleta, CA Design Verification Test Technician II - Contract Staff BS degree in Electronics Technology/Engineering or related science Exp: >1 year |
As a member of the Design Verification team in Goleta, CA, the Test Technician II position holds key responsibilities for ensuring KARL STORZ’s line of video imaging systems continue to maintain their reputation among surgeons and medical staff for delivering world-class quality. The role responsibilities include the following test technician functions: • Using established test procedures to verify that prototypes meet quality standards prior to release to production. • Characterizing the mechanical, electrical, reliability, and imaging performance of existing products and functional models. • Documenting results for internal and external quality and regulatory processes. • Assisting in efforts to troubleshoot product issues related to product quality, manufacturability, reliability, efficacy and regulatory compliance. The engineering environment at KARL STORZ is highly collaborative. The Test Technician II is expected to work closely with other Test Technicians and Engineers to meet product release goals. The Test Technician II is expected to produce high quality test results reports for distribution to internal stakeholders and FDA officials. | 6/15/2022 |
| 6576 | Poseida Therapeutics San Diego, CA Research Associate/Senior Research Associate - Cell Therapy (CAR-T) Research Associate II level, Master's or Bachelor's degree in a Scientific discipline Exp: 0-2 years |
Poseida is seeking an outstanding candidate to join our Immuno-Oncology team and support the development chimeric antigen receptors (CAR-T) cellular therapies against cancer, and other disease areas. The successful candidate will involve bench work, laboratory studies, and the coordination of research projects with the assistance of a senior lab member. | 6/15/2022 |
| 6577 | Precigen Germantown, MD Research Associate, Translational Immunology B.S./ M.S. in Cell Biology, Immunology or related field. Exp: B.S. (0-3+ years); M.S. (0+ years) |
Based in our Germantown, Maryland office Precigen is seeking a Research Associate, Translational Immunology (level determined by candidate experience) to support discovery and preclinical/translational research. We are seeking candidates with exceptional cellular therapy, immunology and immune-oncology research skills looking for a fast paced, exciting working environment utilizing state of the art technology. | 6/15/2022 |
| 6578 | Prominex San Diego, CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
Prominex Inc. is a startup molecular diagnostic company with an experienced team of passionate and energetic scientists driven to create fast and affordable molecular diagnostic solutions across the globe. We are focused on infectious disease assays in point-of-care and home-based settings. We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 6/15/2022 |
| 6579 | Quantapore South San Francisco, CA Research Associate B.S. or M.S. in physics, biochemistry, molecular biology or related field. Exp: 1-3 years |
This position will play a key role in developing Quantapore’s sequencing technology and optimizing the associated procedures and protocols. The candidate will work closely with our experts in biochemistry, molecular biology, bioinformatics and engineering. This position is hands-on and requires operating in a fast-moving environment. | 6/16/2022 |
| 6580 | Rakuten Medical San Diego, CA Research Associate I, Upstream BS/MS Exp: >1 years |
Rakuten Medical is currently looking for a highly motivated individual to support cell line and upstream process development activities. This candidate will join Rakuten Medical ’s CMC team focusing on various aspects of preclinical antibody development including transfection and single cell cloning, cell culture process development, late-stage characterization, technology transfer and research material generation. | 6/16/2022 |
| 6581 | Resilience Alachua, FL SCIENTIST I-II Scientist I: MS Degree in microbiology, biology, molecular biology, biochemistry, chemistry, or related field Exp: 1+ years |
The scientist reports to the Associate Director or Senior Manager of Biologics and performs method development, product and process development, scale up/scale down processing, and performing a wide variety of activities | 6/16/2022 |
| 6582 | Resilience Alachua, FL Research Associate I/II - In Process Testing Research Associate I: BS degree in microbiology, biology, molecular biology, biochemistry, chemistry, or related field Exp: 0-3 years |
The research associate reports to the Senior Manager of In Process Testing and performs routine testing of process development samples. Job duties include, but are not limited to in-process testing for Process Development runs, testing of upstream and downstream samples | 6/16/2022 |
| 6583 | Resilience East Norriton, PA Research Associate II, Process Development, Cell Therapy Bachelor’s or Master’s degree in immunology, cell biology, bioengineering or a related field. Exp: 1-3 years |
Resilience is seeking a talented Research Associate 2 to expand our cell therapy process development team. With the guidance of process development senior staff, this researcher will develop and optimize manufacturing processes for gene-modified cell products to advance Resilience’s biomanufacturing platforms and the clinical programs of Resilience’s partners. | 6/17/2022 |
| 6584 | Resilience East Norriton, PA Research Associate II, Analytical Development, Cell Therapy Bachelor’s or Master’s degree in cell biology, immunology, molecular biology, virology, Exp: 1-3 years |
Resilience is seeking a talented Research Associate 2 to join the Cell Therapy Analytical Development team. This team is responsible for the design, development, and implementation of assays to advance the company’s novel T cell therapy programs. This researcher should have a background in assay development, preferably in molecular and cellular immunology and immune-oncology, while also possessing strong interpersonal skills and the ability to work collaboratively with other groups within the organization. | 6/17/2022 |
| 6585 | Resilience Waltham, MA Research Associate II, Process Development, Stem Cells and Regenerative Medicine Bachelor’s or Master’s degree in cell Biology, immunology or a related discipline Exp: 1+ years |
Resilience is seeking a talented Research Associate II to join us as a valued member of the Cyto Innovation Process Development team. This researcher will focus on hands-on execution of protocols involving induced pluripotent stem cells (iPSCs) for Resilience’s developing Regenerative Medicine Modality. The successful candidate will support the development of Resilience’s best-in-class hypoimmune iPSC generation platform and will collaborate broadly with colleagues in platform R&D, analytical development, and other teams across the Resilience biomanufacturing network. | 6/17/2022 |
| 6586 | Resilience Waltham, MA Research Associate II, Analytical Development, Gene Therapy Master's degree in analytical chemistry, biochemistry, molecular/cellular biology or related field Exp: 1+ (MS) years |
Resilience is building a robust, dynamic, and diverse network of manufacturing capabilities and collaborations – investing in innovation every step of the way. We are looking for a highly motivated Research Associate 2 to contribute to the Gene Therapy Analytical Development group with a focus on cell and molecular assays. Title will be commensurate with relevant experience in analytical development. | 6/17/2022 |
| 6587 | Rocket Pharmaceuticals Cranbury, NJ Research Associate II M. S. in relevant Biological Sciences Exp: 1 year |
Rocket is seeking an individual who will work within the R&D team supporting nonclinical studies to further understand and characterize viral vector constructs for potential therapeutic application in support of Rocket’s gene therapy pipeline. The ideal candidate will have a strong Molecular Biology background, will be highly collaborative, and will adhere to established processes, policies, and quality systems for conducting experiments and reporting data from basic research studies. | 6/17/2022 |
| 6588 | Rockland Immunochemicals Pottstown, PA Scientist I - HCP B.S. in Biology or related fields Exp: 1-3 years |
Responsibilities include: The laboratory skills include basic liquid handling, setting up and performing immunoassays including SDS-PAGE, Western blot, HPLC, biochemistry, antibody and recombinant protein manipulation. Set up and performs immunoassays Strong working knowledge of routine use and maintenance of equipment appropriate to the relevant area Assists with maintenance of work area and maintenance of supplies for team Demonstrates knowledge and efficient use of Outlook Email, Word, Excel, PowerPoint and other required computer applications Demonstrates excellent attention to detail, can work quickly and accurately, organizing tasks and delivering quality with efficiency | 6/17/2022 |
| 6589 | Rockland Immunochemicals Pottstown, PA Scientist I - Recombinant Antibodies Bachelor's or Master’s Degree in Molecular Biology, Immunology, Biological sciences or other related degree Exp: 0– 2 Years |
Rockland Immunochemicals is seeking to hire a highly motivated scientist to join our R&D team. This position of Associate Scientist or Scientist I is to participate in all aspects of recombinant antibody discovery including but not limited to primers design, antibody library construction, antibody sequence analysis, cloning, expression and purification, screening. ALL candidates with background in life sciences or related field are encouraged to apply. Training will be provided accordingly. | 6/17/2022 |
| 6590 | SCA Pharma Windsor, CT Microbiology Analyst - Entry Level 4 year college degree Exp: 0-2 years |
At SCA Pharma, we prepare intravenous medications to be given to patients in hospitals and other healthcare facilities. Our Microbiology lab plays a key role in ensuring the sterily of our facilities and our products, to ensure that only the safest medications leave our facility. As a Microbiology Analyst I, you will be responsible for supporting the Microbiology Department with data processing/entry, Environmental Microbiological testing and Filtration Testing, in addition to daily housekeeping of the laboratory. | 6/17/2022 |
| 6591 | SCA Pharma Little Rock, AR Microbiology Lab Analyst I - Weekend EM Tech Four-year college degree Exp: 0-2 years |
The Microbiology Laboratory Analyst I has the primary responsibility of collecting and processing environmental and personnel monitoring samples in a timely manner and performing microbiological testing in accordance with SOPs and cGMP regulations in the Microbiology Laboratory at SCA Pharma. In addition to sampling procedures, this position will perform aseptic assistance duties and other duties as assigned to support operations of the Micro Lab. This position must work well with others to meet group goals and accomplish routine and time-sensitive laboratory duties. This position will report to the Weekend Shift Senior Microbiologist and act as support staff for testing and investigations pertaining to the Microbiology Laboratory. The individual occupying this position is expected to be capable of working with minimal supervision and communicate effectively with fellow employees as well as Compounding Operations and Quality Assurance departments. Note: Hours for this position are each week Friday through Sunday 0500 to 1700 | 6/17/2022 |
| 6592 | Sebela Pharmaceuticals Holbrook, MA QC Chemist Bachelor’s in chemistry or related field Exp: 1 year |
Conduct routine analytical chemistry testing using various wet chemistry and instrumentation techniques in a regulated cGMP and cGLP environment. | 6/17/2022 |
| 6593 | Sebela Pharmaceuticals Holbrook, MA QC Laboratory Technician Bachelor’s in chemistry or related field Exp: 1 year |
Support the QC workflow and processes in an efficient and effective manner. Provide support to QC Analysts with test preparations. Performs simple / routine chemistry tests. | 6/17/2022 |
| 6594 | Selecta Biosciences Watertown, MA Research Associate I, Quality Control & Analytical Testing B.S./M.S. in Chemistry or related field Exp: 0-2 years |
To support our ambitious pursuits, the Research Associate will produce timely and accurate data and documentation for analyses targeting a variety of nanoparticle components such as small molecules, peptides, proteins, oligosaccharides, and synthetic polymeric material in support of the development of preclinical and clinical products based on Selecta's proprietary ImmTOR® technology. | 6/17/2022 |
| 6595 | Serotiny San Francisco, CA Sr. Research Associate / Scientist – Cell Therapy SRA: MSc. Degree in immunology, cell biology, molecular biology, biotechnology or related area Exp: >1 year |
Serotiny is looking for a Sr. Research Associate / Scientist who is excited to work closely with a team of immunologists and molecular biologists to build and deploy Serotiny's high-throughput C> methods. | 6/17/2022 |
| 6596 | Shine Medical Technologies Janesville, WI Entry Level Chemist Bachelor’s degree in chemistry or related scientific field Exp: Entry Level |
SHINE is immediately seeking a chemistry graduate to help us prepare for, startup, and operate our new medical isotope production facility in Janesville, WI. SHINE is in need of an entry-level chemist to support ongoing research, development, and prototyping work. The role will later transition to be operational and quality-focused, involving preparing reagents and performing chemical analyses for a brand-new facility, currently under construction. Ideal candidates enjoy a fast-paced, challenging environment, where individuals work collaboratively to solve problems on a first-of-a-kind nuclear manufacturing facility that uses innovative technology. A strong desire to learn about radiochemistry, radiopharmaceuticals, and nuclear technology is required. | 6/17/2022 |
| 6597 | Shine Medical Technologies Janesville, WI Entry Level Engineer Bachelor’s degree in engineering, any discipline, or related technical field Exp: Entry Level |
SHINE is immediately seeking engineering graduates to support the construction, licensing, testing, startup, and operation of the new medical isotope production facility in Janesville, WI. SHINE is in need of entry-level engineers to fill a variety of roles outside of a traditional engineering career path. Ideal candidates enjoy a fast-paced, challenging environment, where individuals work collaboratively to solve problems on a first-of-a-kind nuclear manufacturing facility that uses innovative technology. Both hands-on and documentation-focused roles are available. A strong desire to learn and curiosity about nuclear technology is required. | 6/17/2022 |
| 6598 | Shine Medical Technologies Janesville, WI Entry Level Licensing Engineer Bachelor’s degree in engineering, scientific discipline, or related field. Exp: Entry Level |
SHINE is immediately seeking an Entry Level Licensing Engineer to assist the company in the support of the NRC review of the operating license application, the preparation for, and coordination of, NRC construction inspections, support the licensing of commercial and research and development activities conducted under the radioactive materials license, the preparation and submittal of permit applications to other applicable regulatory agencies, and to ensure ongoing compliance with all licenses and permits. The Entry Level Licensing Engineer will work as part of an innovative, collaborative, cross-discipline team to license the SHINE medical isotope production facility. This position will transition from the design and licensing phase, through construction, and into supporting the operation of the facility. | 6/17/2022 |
| 6599 | Sirnaomics Gaithersburg, MD Quality Control Analyst (QC) Bachelors’ or Masters’ degree, or equivalent experience in Chemistry, Biological Science, Biochemistry, Biochemical, Biomedical Engineering or a rela Exp: B.S. : 1-4 years; M.S.: 0-2 years |
Sirnaomics, Inc. is a leading clinical stage biopharmaceutical company in the discovery and development of RNAi therapeutics for treatment of cancer and fibrotic diseases. We are seeking candidates to fill the newly created position of Quality Control Analyst for our headquarters in Gaithersburg, MD. The well-qualified candidate will report directly to the Vice President of CMC of the company and will focus on process development for Polypeptide Nano-Particle (PNP) for siRNA Therapeutic products. The position will bridge the in-house scientific discovery and development with cGMP production and CMC out-sourcing activities, particularly in technology transfer efforts. The individual will also be responsible to optimize parameters for lyophilization and specs for QC assays for product release based on process characterization. | 6/17/2022 |
| 6600 | SIWA Therapeutics Gaithersburg, MD Quality Control Analyst (QC) Bachelors’ or Masters’ degree Exp: BS: 1 - 4 years; MS: 0 – 2 years |
Sirnaomics, Inc. is a leading clinical stage biopharmaceutical company in the discovery and development of RNAi therapeutics for treatment of cancer and fibrotic diseases. We are seeking candidates to fill the newly created position of Quality Control Analyst for our headquarters in Gaithersburg, MD. The well-qualified candidate will report directly to the Vice President of CMC of the company and will focus on process development for Polypeptide Nano-Particle (PNP) for siRNA Therapeutic products. The position will bridge the in-house scientific discovery and development with cGMP production and CMC out-sourcing activities, particularly in technology transfer efforts. The individual will also be responsible to optimize parameters for lyophilization and specs for QC assays for product release based on process characterization. | 6/21/2022 |
| 6601 | MicroVention Aliso Viejo, CA Engineer I/II, Engineering Development Program Bachelor's Degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Industrial Engineering, Chemistry, or other related disci Exp: 0 - 2 years |
This 18 month rotational program is designed to train new Engineers on various aspects of MicroVention Terumo technology procedures, and processes. All candidates will be assigned a Mentor, Peer Mentor, as well as an Advisor to oversee their succession, and will be provided with additional classroom training. Successful candidates will have three (3) six mnonth rotations. Assignments within a rotation will be clearly defined objectives within 3-month increments. These rotations include one (1) required rotation in Manufacturing Engineering and two (2) optional rotations from the following areas: *Research & Development (R&D) *Equipment/Tool Design *Marketing *Regulatory Affairs *Quality *Supply Chain | 6/21/2022 |
| 6602 | Akorn Amityville, NY Chemist I - Finished Products Bachelor's dedree or higher in Chemistry or related field. Exp: 1 year |
The individual will be responsible for providing analytical support to the Department of Quality Control. The individual will be responsible to follow established procedures and protocols to conduct various independent and team driven laboratory experiments. The candidate should assist with the day-to-day maintenance of an orderly QC laboratory such as safety, ordering and receipt of reagents, Instrument calibration. | 6/21/2022 |
| 6603 | SmartPharm Therapeutics San Diego, CA Senior Research Associate-In vivo Efficacy Studies Master's Degree in Life Sciences or related field. Exp: 1-2 years |
The Senior Research Associate will perform in vivo efficacy studies using a novel drug delivery system in animal models of autoimmune disease and cancers. Conducts research and performs laboratory experiments with a high degree of independence and technical mastery. | 6/21/2022 |
| 6604 | SmartPharm Therapeutics San Diego, CA Research Associate-CAR-T In Vivo Bachelor’s Degree in Molecular Biology or related disciplines Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking an experienced Research Associate who will work in the area of development and implementation of in vivo studies to support pre-clinical validation of CAR-T cellular therapies against cancer. The ideal Research Associate applicant has knowledge and hands on experience in cell culture, flow cytometry and mouse models. | 6/21/2022 |
| 6605 | SmartPharm Therapeutics San Diego, CA QC Senior Research Associate/Research Associate Bachelor’s Degree in Molecular Biology or related disciplines Exp: 1+ years |
Sorrento Therapeutics (“Sorrento”) is seeking an experienced Senior Research Associate/Research Associate who will be part of the Analytical Development/Quality Control team to support process development and current Good Manufacturing Practice (cGMP) activities for different viral vectors. | 6/21/2022 |
| 6606 | SmartPharm Therapeutics San Diego, CA Research Associate - CAR-T/DAR-T Bachelor’s Degree in Molecular Biology or related disciplines Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking an experienced Research Associate. We are looking for highly motivated individuals with extensive expertise in molecular and cellular Immunology to join group for next generation of CAR-T/DAR-T technology and product research and development including vector design, molecular cloning, CAR-T generation, and in vitro and in vivo functional assays of engineering T cells. | 6/21/2022 |
| 6607 | SmartPharm Therapeutics San Diego, CA Research Associate - Process Development & Manufacturing Bachelor’s Degree in Molecular Biology or related disciplines Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking a Process Development and MFG Research Associate position to help with protein production and DNA plasmid cGMP production in microbial system including process development and manufacturing. Major tasks include: Buffer preparation, bacteria culture including fermentation in bioreactor and harvest, bacteria lysis and protein and plasmid DNA purification. | 6/21/2022 |
| 6608 | Talaris Therapeutics Louisville, KY Research Assistant Bachelor’s degree in Biology, Immunology of related field of Science Exp: 1 year |
The Research Assistant will be responsible for supporting analytical sample testing related to the research and development of novel cell therapy products under the supervision of a Principal Scientist for preclinical and clinical research studies as well as day-to-day operations related programmatic organization and lab activities. The primary responsibilities of this role include performance of in vitro and in vivo experiments in a mouse model of bone marrow transplantation and recording/analyzing experimental data. Experience working with mouse models is highly desired. Other primary responsibilities of this role are sample processing and performing analytical test methods for preclinical and clinical R&D samples with a focus on flow cytometric analysis and analytical testing for characterization of cell therapy products. | 6/22/2022 |
| 6609 | Talis Biomedical Menlo Park, CA Senior Research Associate MS or equivalent in Molecular Biology, Biochemistry, Biomedical Engineering, Biochemical Engineering, Chemical Engineering Exp: 1-5 years |
We are seeking a highly motivated, talented, and driven Senior Research Associate to join the Assay Development group in the R&D division at Talis Biomedical. This is a great opportunity to join a collaborative and dynamic team effort to enable the development of rapid point-of-care diagnostic tests. The successful candidate will work in product development, including verification and validation activities. You will author, review, and edit SOPs, study protocols, reports, and other documentation as needed. You will work collaboratively with others in Assay Development teams and other departments at Talis, including Assay Research, Operations, Quality, and Engineering. A strong understanding of nucleic acid biochemistry and experience working on cross-functional teams is highly desired. | 6/22/2022 |
| 6610 | Tectonic Therapeutic Watertown, MA Research Associate, In Vivo Pharmacology MS Exp: 1 year |
We are seeking Research Associate (RA) to support our In Vivo Pharmacology efforts across multiple projects. The RA will be responsible for independently performing in vivo studies in animal models across different disease areas. Additional responsibilities include applying a wide range of in vitro and in vivo approaches to understand the mechanism of action of various therapeutic agents. The RA will interact seamlessly with Discovery Immunology and other Discovery groups to help execute on company strategy. The major focus of this position will be the in vivo evaluation of novel biologicals, including antibody-based approaches that will support the drug discovery efforts across multiple programs from target validation to identification of clinical candidates. | 6/22/2022 |
| 6611 | Tectonic Therapeutic Watertown, MA Research Associate – Cell Pharmacology Bachelor’s degree in Biology, Pharmacology, Biochemistry or related discipline Exp: 1-3 years |
We are looking for a highly collaborative team player who has experience in cell-based signaling studies for studying biological drug products. Hands-on experience with mammalian cell culture is required with expertise in cell and molecular biology techniques preferred. The successful candidate will contribute to our core research capabilities and the development of our anti-GPCR antibody discovery platform. The candidate would support assay development and conduct established assays to validate new targets and characterize the in-vitro function of antibodies. This position represents a unique opportunity for the successful applicant to join an innovative start-up at the heart of the Boston biotech ecosystem and to contribute to its long-term success. | 6/22/2022 |
| 6612 | Toxikon Greenfield, IN Study Technician (Research Assistant) - Anatomic Pathology Bachelor’s Degree in Life Sciences, or Associate Degree in Histology, Laboratory Animals Technology or Veterinary Technology; experience may substitut Exp: NO PROFESSIONAL LAB EXPERIENCE REQUIRED - WE TRAIN! |
We are seeking talented science majors in the fields of Biology, Physiology, Animal Science, Zoology, Neuroscience, Biochemistry, Genetics, Microbiology, Immunology and similar majors to work as a Pathology Study Technician (Research Assistant) in Greenfield, IN. Sign-on Bonus: $4,000 ($2,000 upon hire and $2,000 after 6 months; external candidates only) Labcorp Drug Development's work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life-saving work and help improve patients' lives while growing your career. In this role, you will perform basic necropsy or histology tasks on a variety of laboratory animals in compliance with the appropriate Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs) and regulatory guidelines. You will also monitor animal health and welfare in compliance with the Animal Health and Welfare Act and help maintain facilities for Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC) compliance. | 6/23/2022 |
| 6613 | Toxikon Somerset, NJ Study Technician - Research Animal Operations Bachelor degree in Life Sciences Exp: No experience is required with a Bachelor Degree |
Explore research careers and be a part of something bigger! Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. Our work in developing new pharmaceutical solutions has an incredible impact on the quality of lives of millions worldwide. We have an excellent opportunity for a Study Technician-Animal Operations to join our team in Somerset, NJ. The Study Technician is part of a division that supports preclinical work- in vivo toxicology, PK, metabolism, and safety studies as part of the drug development process. $4,000 Sign On Bonus offered to new hires! | 6/23/2022 |
| 6614 | Toxikon Greenfield, IN Formulations Lab Technician-Study Tech Dose Formulations BS degree in Chemistry, Biology or other related fields. Exp: not required |
Formulations Lab Technician-Study Tech Dose Formulations -Greenfield Indiana $18.00 per hour minimum with 5% shift premium and .50 increase at 6 months. $4,000 sign on bonus! Day shift hours-4-10 hour days once fully trained What will you be doing? Preparing formulations for research studies that are evaluating the safety, effectiveness of new drugs and/or chemicals used on crops. Common duties include preparing laboratory reagents, vehicles, diets, solution/suspensions, and capsules according to study protocols. Extensive training provided! In this position your work matters! You will be joining Labcorp Drug Development mission to delivering healthcare breakthroughs. | 6/23/2022 |
| 6615 | Toxikon Somerset, NJ Study Technician Pathology Bachelor degree in Life Sciences Exp: No experience is required with a Bachelor Degree |
Explore research careers and be a part of something bigger! Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. Our work in developing new pharmaceutical solutions has an incredible impact on the quality of lives of millions worldwide. We have an excellent opportunity for a Study Technician-Pathology to join our team in Somerset, NJ. The Study Technician is part of a division that supports preclinical work and safety studies as part of the drug development process. Starting at $18.00 per hour and Up (based on experience) $4,000 Sign On Bonus offered to new hires! | 6/23/2022 |
| 6616 | Toxikon South San Francisco, CA Lab Technician - Entry level, will train! BS/BA in Biology, Chemistry or similar scientific discipline required Exp: No previous experience required |
Monogram Biosciences, part of LabCorp, is seeking a Cell Culture Technician to join its Support Operations team in South San Francisco! As part of the Cell Culture and Critical Reagent group, this position will work in a highly collaborative team environment. This is a great entry-level opportunity to join an innovative organization and receive targeted one-on-one training that will help the individual grow in a career in the biotechnology field. This position will not be working inside the clinical laboratory. The schedule for this position will be Tuesday-Saturday, 6:00am-230pm. During training, schedule will be Monday-Friday. | 6/23/2022 |
| 6617 | Toxikon RTP, NC Cytogenetics Technologist Trainee - Entry Level, Will Train! Bachelors in Biology, Chemistry, or relatable life science field Exp: not required |
The Integrated Genetics Division is seeking a Cytogenetics Technologist Trainee to join their Cytogenetics Prenatal team! The Technologist Trainee will be working in a clinical diagnostics laboratory setting, testing patient specimens. Assays (tests) performed in the Cytogenetics Department utilize a variety of scientific techniques, including specimen culturing, slide preparation, and chromosome analysis. This is a great entry level opportunity to join an innovative laboratory and receive targeted one-on-one training that will help the individual grow in a career in the clinical laboratory field! (Note: this is not a research job). Participate in LabCorp's in-house training program for the field of Cytogenetics. Receive in depth training and preparation for the ASCP board examination and ASCP-CG certification. Training program is a two year commitment and requires signing a training reimbursement agreement. The schedule for this position will be Tuesday – Saturday, 7:00am-3:30pm. | 6/23/2022 |
| 6618 | Trevigen Minneapolis, MN Advanced Research Associate Master’s degree in a related field Exp: up to 2 years |
This position is responsible for participating in the development of Bio-Techne's various product lines. You will maintain knowledge of multiple products and procedures as well as draft and revise standard operating procedures in order to further the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 6/23/2022 |
| 6619 | Trevigen Newark, CA Research Associate BS in biology, chemistry, life science, or related field Exp: 0-2 years |
We seek a highly motivated and creative Research Associate to join our R&D team. You will work within a highly dynamic and creative group and be responsible for developing new products and improving current products based on RNAscope technology. | 6/23/2022 |
| 6620 | Trevigen Minneapolis, MN Advanced Research Associate, Protein Development (Cell Culture) Bachelor’s degree required in microbiology, biology, biochemistry, bioprocess engineering, chemistry, or an equivalent Exp: 0-2 years |
A Research Associate is responsible for development of cell culture protocols for new recombinant protein products. This includes screening clones and testing growth conditions and media formulations in bioreactors and other culture formats, in small to medium scale. It may also include cooperation with the molecular biology group in creation of new clones, creation and characterization of new cell lines, and screening studies in search for novel protein product targets. This position will work with stable cell line expression systems as well as transient expression platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 6/23/2022 |
| 6621 | Trevigen Newark, CA Research Associate, R&D BS in molecular biology, biochemistry, cell biology or related field Exp: 1 year |
We seek a highly motivated and creative research associate to join our R&D team. You will work within a highly dynamic group and be responsible for improving current products and developing new products based on RNAscope technology. | 6/23/2022 |
| 6622 | Trevigen Minneapolis, MN Research Associate - Cell Culture Development Bachelor’s degree Exp: 0-2 years |
A Research Associate is responsible for development of cell culture protocols for new recombinant protein products. This includes screening clones and testing growth conditions in bioreactors and other culture formats, in small to medium scale. It may also include cooperation with the molecular biology group in creation of new clones and clone libraries, creation and characterization of new cell lines, and screening studies in search for novel protein product targets. | 6/23/2022 |
| 6623 | Trevigen Minneapolis, MN Advanced Research Associate GMP Master’s degree in degree in Biology, Biotechnology , or a related field. Exp: 1 year |
The responsibilities of this position are to manufacture protein purification reagents/kits to restock the supply of existing products and modify and validate existing protocols for larger scale production of these reagents/kits. Duties include: Perform expression and purification of proteins for restock utilizing High Performance Liquid Chromatography method in the AKTA system; analyze biological data to and make decisions to create a process that delivers consistent product/process to meet quality and performance specifications; research protein purification protocol modifications for large-scale purification (process development); rewrite purification protocols after process modifications for process methods; implement Correction Action Preventive Actions (CAPA’s); conduct equipment calibration and maintain lab equipment including TFF (tangential flow filtration), pumps, chromatography columns, AKTA systems, aseptic filters, and bench equipment, concentrators, and pH meter, and contracts repair service when needed; maintain lab order and cleanliness; dispense and label reagent product; assist in raw material and product inventory control; prepare aseptic filter and aliquot product for bulk storage; prepare common buffers and reagents; improve operation efficiency and contribute to reducing costs; generate and maintain equipment validation and process SOPs (Standard Operating Procedures); develop and validate new Good documentation practices (GDP) and Current Good Manufacturing Practices (cGMP) for protein purification process development; work with supervisor and manager to facilitate scheduling of starting material; maintain compliance with the lab’s quality training and documentation; follow company policies and practices as outlined in the Handbook and follows safety guidelines according to the AWAIR (A Workplace Accident and Injury Reduction Program), Chemical Hygiene and Exposure Control manuals; Column chromatography; HPLC operations and mechanisms using AKTA system; process equipment including TFF, pumps, chromatography columns, aseptic filters, and bench equipment; writing processing protocols to purify proteins; generation and maintenance of process SOPs; good documentation practices (GDP) and Current Good Manufacturing Practices (cGMP); biological data analytics; corrective Action Preventive Action (CAPA’s); safety guidelines according to the AWAIR (A Workplace Accident and Injury Reduction Program), Chemical Hygiene and Exposure Control manua | 6/23/2022 |
| 6624 | Unity Biotechnology South San Francisco, CA RESEARCH ASSOCIATE 1 OR 2, IN VIVO PHARMACOLOGY Bachelor’s degree Exp: 1-4 years |
We are seeking to hire an exceptional Research Associate to join the in vivo pharmacology team. This position will be a critical part of a highly dynamic scientific research group supporting the characterization and development of drug candidates against novel drug targets. This role affords the individual the opportunity to work closely with a multi-disciplinary team, to deepen their expertise and knowledge in drug discovery, and to make key contributions to help bring new medicines to patients. | 6/23/2022 |
| 6625 | Unity Biotechnology South San Francisco, CA RESEARCH ASSOCIATE 1 OR 2, IN VITRO PHARMACOLOGY Master’s degree in biochemistry, cellular and molecular biology or a related field Exp: 1 years |
Unity Biotechnology is seeking to hire a motivated and diligent Research Associate 1 / 2. The ideal candidate is an openminded and curious team player, who enjoys problemsolving and collaborating with other team members to further the research objectives of the Discovery organization This is a lab-based position focused on performing a variety of in vitro assays including, cell-based assays, biochemical assays, and MSD-based ELISA assays, and other molecular biology techniques. The candidate will be responsible for experimental design, execution, analysis, and presentation to the project team. This individual will play a key role in supporting a advancement of large molecule candidate through in vitro studies. | 6/23/2022 |
| 6626 | Universal Cells Seattle, WA Research Associate I, Clinical Gene Editing in Seattle, Washington BS Degree Exp: 0-3 years |
The primary purpose of the Research Associate I is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This entry-level Research Associate role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. This position will be provided training to perform all required fundamental skills to include record keeping, aseptic technique/cell culture, general lab operations, equipment use and maintenance, and some troubleshooting. Will assist with basic laboratory operations, and will keep appropriate documentation, including lab notebooks, batch documentation and experimental summaries. May assist in preparing controlled documents and data summaries. | 6/23/2022 |
| 6627 | Universal Cells South San Francisco, CA Research Associate I, Vector Biosciences in South San Francisco, California Master's Degree in Molecular Biology, Biology, Life Sciences or a related discipline Exp: 1+ years |
The Research Associate will support the Vector Biosciences team and assist with the development of novel AAV gene therapy vectors using molecular biology techniques. The Research Associate will be located in our South San Francisco R&D laboratories. | 6/23/2022 |
| 6628 | Universal Cells Westborough, MA Research Associate II, Cell Biology in Westborough, Massachusetts MS Exp: 0+ years |
This position plays a key role in developing human pluripotent stem cell (PSC)-derived ocular cells for clinical applications. The successful candidate will have a track record of success in a collaborative research environment with proficiency in standard cell culture and cell characterization techniques, and a proven ability to execute experiments and analyze data independently | 6/23/2022 |
| 6629 | Universal Cells South San Francisco, CA Research Associate II, in vivo in South San Francisco, California MS Exp: 0-2 years |
The primary purpose of the Research Associate II is to support in vivo pharmacology activities by performing cell culture and immunological assays, analyzing data, and drafting reports. This individual will work primarily in a laboratory setting to advance CAR adoptive cell therapy programs for treatment of cancer | 6/23/2022 |
| 6630 | Universal Cells Westborough, MA Research Associate I/ II Stem Cell Biology in Westborough, Massachusetts RA I: BS; RA II: MS Exp: RA I: 0-3 years; RA II: 0-2 years |
We are seeking a highly motivated and talented Research Associate I/II to join our Research team and play a key role in developing human pluripotent stem cell (PSC)-derived macrophages for clinical applications. The successful candidate will have a track record of success in a collaborative research environment with proficiency in pluripotent stem cell culture, various standard immunology and cell biology techniques and a proven ability to plan and execute experiments and analyze data independently. The Research Associate will apply their knowledge of pluripotent stem cell culture and immune cell assays towards the generation of an exciting cell therapy opportunity | 6/23/2022 |
| 6631 | Universal Cells South San Francisco, CA Research Associate II, Vector Biosciences in South San Francisco, California Bachelor's degree in Molecular Biology, Biology, Life Sciences, or a related discipline Exp: 1+ years |
The Research Associate will support the Vector Biosciences team and assist in developing novel in vitro models and assays for testing AAV vector products potency. The Research Associate will be located in our South San Francisco R&D laboratories. | 6/23/2022 |
| 6632 | Wave Life Sciences Cambridge, MA Research Associate/Associate Scientist, CNS Biology MS degree Exp: 1-2 years |
Wave is seeking an experienced and highly motivated biologist to join its research team in Cambridge, Massachusetts. This is an ideal position for an individual with a strong background in drug discovery and early drug development who thrives in a team-oriented, fast-paced, and cross disciplinary biotech environment. This successful candidate will contribute to all levels of discovery research to support development of optimized nucleic acid therapies for Central Nervous System (CNS) disorders. | 6/23/2022 |
| 6633 | Wave Life Sciences Cambridge, MA Associate Scientist/Scientist, Medicinal/Organic Chemistry BS, MS or PhD Exp: 0-2 years |
Wave is seeking a highly motivated synthetic organic chemist to join the Medicinal Chemistry team in Cambridge, MA. This position is ideal for a chemist who is interested in learning cutting edge technologies that thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. This individual will be responsible for planning, designing, and executing multi-step synthesis including purification and compound characterization. Active collaboration with colleagues across disciplines, participation in project team meetings, and contribution toward creative problem solving are all encouraged. | 6/24/2022 |
| 6634 | Frontage Hayward, CA Research Associate M.S. degree in related scientific discipline Exp: 0-3 years |
Job Summary 1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 6/24/2022 |
| 6635 | Frontage Hayward, CA Research Associate M.S. degree in related scientific discipline or B.S degree Exp: 0-3 years |
Job Summary 1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 6/24/2022 |
| 6636 | Frontage Hayward, CA Research Associate-Biologics MS / MA in biochemistry, biology, chemistry, pharmaceutics or related scientific discipline Exp: 0-2 years |
Job Summary Conduct study design, lab-testing, data analysis and PI review. Author and/or review methods, protocols and other related documents. Assist PIs in maintaining project quality, meeting compliance requirements and timelines. Prepare notebooks, study binders, data packets, data summaries, methods, and qualification/validation protocols under the supervision of lab management / PIs Monitor reagent and consumable inventories and timely submit the orders for the support of both project and non-project based programs After receiving sufficient training, perform as PI and manage the overall planning, execution, and quality of assigned MD/MV and sample analysis projects under the supervision of lab management Participate TC and communicate with sponsors to solve technical issues and update projects, provide weekly summary to the sponsors | 6/24/2022 |
| 6637 | Frontage Hayward, CA Research Assistant- Bioanalytical Services B.S. degree in related scientific discipline. Exp: 0-3 years |
Job Summary 1) Assist lab work and method development 2) Follow SOP and protocol to conduct method validation and sample analysis under supervision 3) Comply with GLP regulations in lab work and documentation 4) QC review data and reports 5) Perform instrument setup, maintenance, and basic trouble-shooting under supervision 6) Strictly follow SOPs and regulations to serve as sample coordinator. | 6/24/2022 |
| 6638 | Frontage Chicago, IL Analytical Chemist B.S. degree in chemistry Exp: 0-3 years |
Key Responsibilities Duties include methods transfer/development and validation, determination of analytes in dose formulations and accurate preparation of formulations (e.g., solutions, suspensions, etc.) to be used in toxicology studies. Knowledge of performing these duties with strict adherence to Good Laboratory Practice Regulations (FDA, EPA and OECD) is a plus. Other responsibilities as assigned. | 6/24/2022 |
| 6639 | Frontage Exton, PA Scientist/Associate Scientist- Cell Culture B.S. or M.S. in molecular biology, biochemistry, biophysics, immunology, or a related field Exp: 1 year |
Position Summary This is a bench scientific position for a competent and hardworking scientist with experience in protein purification and/or labeling of protein reagents. The person will be responsible labeling of reagents (protein and antibodies), purification and characterization including concentration estimation, SDS-PAGE, SE-HPLC, endotoxin estimations etc. He/she will be responsible for the quality of final product, record keeping and interacting with end user. The position will require excellent communication skills, and basic computer skills. | 6/24/2022 |
| 6640 | Karius Redwood City, CA Research Associate, Automation Bachelor’s degree in Biology, Molecular Biology, or related field Exp: 1-3 years |
As Research Associate in Automation you will work alongside the Research and Production teams to automate NGS-based infectious disease diagnostics providing meaningful contributions to making an impact in the lives of patients while contributing to the company’s growth and development. You will have the opportunity to learn and support process excellence by assisting with maintenance, testing, and programming for Hamilton liquid handlers used to deliver NGS infectious disease diagnostic assays for our CLIA production lab. The ideal candidate should have experience working in a laboratory environment, have an interest in automation, and be willing to be challenged and learn new skills | 6/6/2022 |
| 6641 | Karius Redwood City, CA Research Associate B.S. (Master’s degree preferred) in Biology, Molecular Biology, Genetics or related field. Exp: 0-2 years |
As a Research Associate, you will work alongside scientific leaders in NGS-based infectious disease diagnostics providing meaningful contributions to making an impact in the lives of patients while contributing to the company’s growth and development. You will have the opportunity to maintain process excellence for a state-of-the-art NGS infectious disease diagnostic assay by assisting in an established in-house manufacturing process. You will be also involved with several exciting research projects and be at the forefront of non-invasive diagnostics working alongside our scientists to deliver new products. The ideal candidate should have some limited experience with nucleic acids, NGS, or other molecular biology assays to conduct laboratory experiments on research projects under the direction of senior lab personnel. | 6/6/2022 |
| 6642 | KVK Tech Newtown, PA Chemist Bachelor of Science Degree, Master’s Degree is highly preferred Exp: 1-4 + years |
Perform analytical testing of raw materials, in-process materials, stability samples, finished products and product development products using different analytical techniques. | 6/6/2022 |
| 6643 | Liquidia Morrisville, NC Quality Associate BS degree required, preferably in a technical field Exp: 0-2 years |
We are looking for a Quality Associate to perform various activities within the Quality Department. The primary function is to ensure all documentation created and completed is as per the company Quality Management System (QMS). This includes drafting and approving documents and assessing compliance of manufacturing, testing, and/or clinical activities. You will be required to be a detail-oriented person with strong communication and organizational skills. | 6/6/2022 |
| 6644 | Lygos Berkeley, CA Fermentation Research Associate, Entry-Level B.S. or equivalent degree in chemical engineering, or related field Exp: 0-4 years |
Lygos is seeking an entry-level Fermentation Research Associate to set up, run, clean, and maintain bench-top level bioreactors (0.5L - 15L) and to develop processes and evaluate strains producing a variety of products. The successful candidate will have experience with general lab procedures, sterile technique, and data interpretation / reporting and be comfortable in a fast paced and dynamic work environment. | 6/8/2022 |
| 6645 | Manifold Bio Boston, MA Research Associate: Cell Assays & Screening B.A./B.S./M.S. degree in biology, biochemistry, bioengineering or similar Exp: one year |
Manifold Bio is seeking an enthusiastic, creative Research Associate or Senior Research Associate to join our growing team in our mission of multiplexed, in vivo drug discovery. The ideal candidate will have experience in molecular biology, mammalian cell culture and/or screening assays. In this role, you will contribute to advancing Manifold’s ambitious drug discovery programs using high-throughput and multiplexed screening technologies including Manifold’s proprietary protein barcoding technology. | 6/8/2022 |
| 6646 | Masy Bioservices Morrisville, NC Data Review Specialist, Chemistry Master’s degree in Chemistry, Biology, or related field Exp: 1+ years |
The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing various activities at range of complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and process inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance-oriented training as necessary. The QC Data Review Specialist assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. Business needs and deadlines will require employee to perform work duties outside of standard work hours on occasion. | 6/9/2022 |
| 6647 | Masy Bioservices Morrisville, NC Data Review Specialist, Microbiology Master’s degree in Chemistry, Biology, or related field Exp: 1+ years |
The QC Data Review Specialist is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and process inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as necessary. The QC Data Review Specialist assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. Business needs and deadlines will require employee to perform work duties outside of standard work hours on occasion. | 6/9/2022 |
| 6648 | Masy Bioservices St Louis, MO QC Data Review Specialist, Chemistry Master’s degree in Chemistry, Biology, or related field Exp: 1+ years |
The Quality Control Data Review Specialist is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and process inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as necessary. The QC Data Review Specialist assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. Business needs and deadlines will require employee to perform work duties outside of standard work hours on occasion. | 6/9/2022 |
| 6649 | Masy Bioservices Morrisville, NC Associate Scientist II - Raw Materials Bachelor's degree in in Pharmaceutical Sciences or Chemistry or Master's degree Exp: BS: 1 years; MS: 0 experience |
The position is responsible for support of compendial testing group and manages priorities of this team to provide the timely, compliant and accurate testing of raw materials, critical utilities, in-process samples and finished product. This position will collaborate with cross-functional teams and will work side-by-side with other scientists and professionals to drive the scientific agenda. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile.CURRENTLY OFFERING ***Up To $3,000 SIGN ON BONUS*** | 6/9/2022 |
| 6650 | Maze Therapeutics South San Francisco, CA Research Associate / Senior Research Associate, Stem Cell Biology (Contract) M.S. in relevant discipline Exp: 1+ years |
The Stem Cell Biology is looking for a talented and highly motivated researcher with experience in molecular and cellular biology to contribute to projects developing stem cell models for drug discovery for a variety of therapeutic areas. The successful candidate will have a thorough understanding of molecular biology with familiarity in human pluripotent stem cells (hiPSCs/hESCs). Additional experience with CRISPR gene editing, assay development, and high throughput screening is preferred. As a member of the stem cell group, you will work alongside stem cell scientists to support the growth of new differentiations, assays, and screens. This is an exciting interdisciplinary role in a dynamic cross-functional team that will contribute directly to the identification of new targets and the design and validation of novel disease-modifying therapeutics. | 6/9/2022 |
| 6651 | Maze Therapeutics South San Francisco, CA Research Associate / Senior Research Associate, Functional Genomics (Contract) BS/MS in a biological science discipline Exp: 1 - 3 years |
The Functional Genomics team is looking for a talented and highly motivated Research Associate with molecular biology and cell culture experience to join our functional genomics team. This person will support functional genomics scientists in execution of genome-wide screens (such as CRISPR). | 6/9/2022 |
| 6652 | MDxHealth Irvine, CA Laboratory Technician I (Shift: Tuesday to Saturday 8:00am - 4:30pm) Bachelor's degree preferred Exp: 1 to 2 years |
The Laboratory Technician I tasks will include specimen preparation, preparation and management of reagents and supplies, instrument preventive maintenance and troubleshooting and assisting in the performance of quality control procedures. | 6/9/2022 |
| 6653 | MDxHealth Plano, TX Laboratory Technologist - Plano, TX Location PART TIME (Shift Sunday to Tuesday 9:00 a.m. - 5:30 p.m.) (Flexible Hours) Bachelor's degree. in life science related field (e.g., biology, chemistry, biochemistry, microbiology) required and ASCP Certification preferred Exp: 1 year |
The Laboratory Technologist will implement the development of new assays within clinical Microbiology and Molecular Biology disciplines in clinical laboratory operations, and performs the processing of patient samples using manual microbiology techniques and molecular biology protocols governed by MDxHealth's Quality Systems and Technical Standard Operating Procedures. | 6/9/2022 |
| 6654 | MDxHealth Plano, TX Laboratory Technician I - Plano, TX Location - PART TIME (Shift: Sunday to Tuesday 9:00am - 5:30pm) (Flexible Hours) Laboratory Technician I - Plano, Bachelor's degree preferred Exp: 1 to 2 years |
The Laboratory Technician I tasks will include specimen preparation, preparation and management of reagents and supplies, instrument preventive maintenance and troubleshooting and assisting in the performance of quality control procedures. | 6/9/2022 |
| 6655 | MDxHealth Plano, TX Laboratory Technologist - Plano, TX Location (Shift Wednesday to Saturday 9:00 a.m. - 7:30 p.m.) (Flexible Hours) Bachelor's degree. in life science related field (e.g., biology, chemistry, biochemistry, microbiology) required and ASCP Certification preferred Exp: 1 year |
The Laboratory Technologist will implement the development of new assays within clinical Microbiology and Molecular Biology disciplines in clinical laboratory operations, and performs the processing of patient samples using manual microbiology techniques and molecular biology protocols governed by MDxHealth's Quality Systems and Technical Standard Operating Procedures. | 6/9/2022 |
| 6656 | MDxHealth Plano, TX Laboratory Technician I - Plano, TX Location (Shift: Tuesday to Friday 9:00am - 7:30pm) (Flexible Hours) Bachelor's degree preferred Exp: 1 to 2 years |
The Laboratory Technician I tasks will include specimen preparation, preparation and management of reagents and supplies, instrument preventive maintenance and troubleshooting and assisting in the performance of quality control procedures. | 6/9/2022 |
| 6657 | MDxHealth Plano, TX Laboratory Technologist - Plano, TX Location (Shift Tuesday to Saturday 10:00 a.m. - 6:30 p.m.) (Flexible Hours) Bachelor's degree. in life science related field (e.g., biology, chemistry, biochemistry, microbiology) required and ASCP Certification preferred Exp: 1 year |
The Laboratory Technologist will implement the development of new assays within clinical Microbiology and Molecular Biology disciplines in clinical laboratory operations, and performs the processing of patient samples using manual microbiology techniques and molecular biology protocols governed by MDxHealth's Quality Systems and Technical Standard Operating Procedures. | 6/9/2022 |
| 6658 | Mekonos Berkeley, CA Research Associate, Chemistry B.S or M.S in Chemistry, Chemical Engineering, Material Science, Biochemistry or a related discipline Exp: 1-3 years |
Mekonos is an early stage deep-tech startup that is transforming scalable cell engineering. In this role, you will work beside wet lab scientists and hardware engineers to further the development of our silicon chip based cell engineering platform. We are looking for resourceful, highly motivated people interested in a multidisciplinary role at a fast growing company. Talented individuals will have the opportunity to craft their responsibilities to best fit their unique skills and interests. | 6/9/2022 |
| 6659 | Minnetronix Medical St. Paul, MN Mechanical Engineer I BS degree or equivalent in Mechanical Engineering or Physics Exp: 0-3 years - entry level |
Mechanical Engineers apply Minnetronix Standard Operating Procedures and broad, in depth knowledge of mechanical engineering industry best practices, standards and technology areas to design, implement, and test medical device systems. Mechanical Engineers I will be skilled at mechanical design, drawings, prototype fabrication, design for manufacturability, production processes, and the testing necessary to support new product designs. They work under close engineering supervision in a team environment. | 6/9/2022 |
| 6660 | Myriad Genetics Salt Lake City, UT Research Associate I BS or higher degree in Biology, Chemistry, or related science Exp: 1-3 years |
This research associate role is part of our Translational Development team and is responsible for developing and transferring technologies and product upgrades from R&D to our CLIA laboratory. The role requires a wide breadth of knowledge in wet and dry bench skills and an eagerness to collaborate across multiple disciplines at Myriad Women’s Health. | 6/9/2022 |
| 6661 | Myriad Genetics Salt Lake City, UT Research Associate I BS or higher degree in Biology, Chemistry, or related science Exp: 1-3 years |
This research associate role is part of our Translational Development team and is responsible for developing and transferring technologies and product upgrades from R&D to our CLIA laboratory. The role requires a wide breadth of knowledge in wet and dry bench skills and an eagerness to collaborate across multiple disciplines at Myriad Women’s Health. | 6/9/2022 |
| 6662 | Myriad - RBM Austin, TX Assay Development Associate Scientist Bachelor's degree in relevant scientific discipline Required Exp: 1 year |
The Scientist for Assay Development contributes to the design of and is responsible for experiment execution of assay/method development. | 6/9/2022 |
| 6663 | NAMSA Northwood, OH Lab Technologist - In Vivo Bachelor’s degree in scientific discipline Exp: one year |
Come and work for an organization whose: Mission is to make a scientific contribution to every medical device in the world. Culture is passionately committed to the partnership between one another and our clients to improve and save lives through a respectful, trusting, and collaborative environment. Values have stood the test of time. Above all else, conduct ourselves with integrity | 6/9/2022 |
| 6664 | NAMSA Northwood, OH Chemist Master’s degree Exp: no experience |
NAMSA is a rapidly growing, global organization. We are always looking to connect with top talent in our industry. If you are interested in learning more about NAMSA and the FUTURE position below, please apply today! NAMSA is a rapidly growing, global organization. We are always looking to connect with top talent in our industry. If you are interested in learning more about NAMSA and the FUTURE position below, please apply today! | 6/9/2022 |
| 6665 | NAMSA Northwood, OH UPLC Chemist - Interpretation Master's degree Exp: no experience |
Come and work for an organization whose: Mission is to make a scientific contribution to every medical device in the world. Culture is passionately committed to the partnership between one another and our clients to improve and save lives through a respectful, trusting, and collaborative environment. Values have stood the test of time. Above all else, conduct ourselves with integrity | 6/9/2022 |
| 6666 | Nanomix San Leandro, CA Research Associate Bachelor of Science (or foreign equivalent) in in Chemistry, Chemical Engineering, Biology, Bioengineering or related field Exp: three (3) months |
Design and develop new cartridge prototypes, working with biosensors, filters, conjugate pads, microfluidics, device programming, etc. to enable specific biological assays on the eLab platform. Design processes required to manufacture product components by developing fixtures (CAD, Laser Printer, 3D Printer, Solidworks etc.), installing necessary components on machinery (Vacuum, Pressure Gauge, Pressure Regulator etc.), scripting robotic liquid handlers, drafting qualification requirements, and writing quality documentations. Design and execute biological wet lab experiments using ELISA, enzymatic assays, chromogenic assays, fluorescence/chemiluminescence. Work with electrochemical (CV, chronocoulommetry) and analytical (FTIR, Raman) tools to characterize biosensors and their performance. Develop quality control methods and implement them in the quality system. Perform large scale data analysis using JMP, PRISM, MATLAB, and Python to analyze research data and manufacturing data. | 6/9/2022 |
| 6667 | nanoComposix San Diego, CA Research Associate: Lateral Flow B.Sc. OR M.Sc. Exp: BSc.: 3+ months; MSc.: 0 years |
Develop nanoparticle-based lateral flow diagnostics for scientific contracts, grants, and commercial projects. Assemble, run, and optimize lateral flow diagnostic assays to increase sensitivity and minimize non-specific background Preform standard procedures for assay development, including functionalizing nanoparticles, purifying antibodies, striping membranes, running tests, interpreting data, buffer preparation, and running BCA and ELISA assays Operate lateral flow equipment, including the striper, guillotine, laminator, pH probe, nano-drop, and UV-vis Document procedures, observations, and results and independently identify successes and failures Communicate with team members, managers, and customers to share results and discuss future directions | 6/9/2022 |
| 6668 | nanoComposix San Diego, CA Research Associate: Nanoparticle Synthesis Bachelors degree in Chemistry or related field Exp: 1 year |
Scientific tasks which may include fabrication and characterization of nanoparticles for product inventory and custom orders. Fabricate and characterize standard products with high reproducibility Meticulously document production into lab and electronic notebooks and forms associated with quality system Discuss and analyzes findings with co-workers and managers to collectively select logical tasks to be completed next Independently find solutions to problems by asking questions and reading relevant scientific literature Prioritize synthesis tasks to minimize back-orders with manager input and communicate status of production to managers | 6/9/2022 |
| 6669 | nanoComposix San Diego, CA Research Scientist: Lateral Flow M.Sc. Exp: 0+ years |
Develop nanoparticle-based lateral flow diagnostics for scientific contracts, grants, and commercial projects. Independently conduct and direct lateral flow development research projects with a high level of independence on time and within budget Draft and execute technical R&D plans, document experiments, and communicate repeatable results to others Prioritize tasks, anticipate next steps, and multitask effectively to balance quality with throughput Suggest and implement system solutions as needed Provide direct reports with clear instructions and empower them to prioritize tasks Demonstrate and assist team members with challenging technical tasks Cooperate with changing demands, priorities, and personalities | 6/9/2022 |
| 6670 | nanoComposix San Diego, CA Research Scientist: Nanoparticle Synthesis M.Sc. Exp: 0+ years |
Support nanoparticle development for scientific contracts, grants, and commercial projects through technical and management responsibilities. Independently conduct and direct research projects with a high level of independence for a timely completion within a budget Draft and execute technical R&D plans, document experiments, and communicate repeatable results to others Prioritize tasks, anticipate next steps, and multitask effectively to balance quality with throughput Suggest and implement system solutions as needed Provide direct reports with clear instructions and empower them to prioritize tasks Demonstrate and assist team members with challenging technical tasks Cooperate with changing demands, priorities, and personalities | 6/9/2022 |
| 6671 | NantKWest El Segundo, CA Process Engineer, Downstream BS or MS degree in Chemistry/Biochemistry/Biochemical Engineering Exp: 0-5 years |
The Process Engineer - Downstream is a member of the Process Science team and will provide process development and engineering support focused on downstream purification operations. The Process Engineer will work on process development and characterization, tech transfer scale up, and process improvements for ImmunityBio’s diverse product pipeline. | 6/9/2022 |
| 6672 | NantKWest Culver City, CA Quality Control Analytical Associate Bachelor Science degree in Biochemistry or related discipline Exp: 1 years |
The Quality Control Analytical Associate will provide testing support for various cell therapy programs through lot release assays such as Flow Cytometry and Cell Based Potency assays. Additionally, the position will support sample preparation teams, complete investigations, and operations such as cell culture, sample thawing and preparation, lab equipment preventive maintenance, buffer preparation, supply inventory management, and general support tasks in order to allow the lab to continuously operate. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in an efficient, highly interactive, goal-oriented team environment. | 6/9/2022 |
| 6673 | NantKWest El Segundo, CA Validation Engineer BS in engineering or relevant technical discipline Exp: 0-2 years |
ImmunityBio is developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. The Validation Engineer is responsible for generating and executing protocols, creating summary reports and executing validation activities in FDA regulated biopharmaceutical environments. Coordinates all validation activities by constant communication with affected departments and personnel. Will report to a manager or head of the department. The Validation Engineer I works on projects/matters of limited complexity in a support role. | 6/9/2022 |
| 6674 | NantKWest El Segundo, CA Manufacturing Associate Bachelor’s of Science or Master’s of Science in Chemical Engineering, Genetics, Molecular Biology, Biotechnology, Microbiology, Biochemistry, or a rel Exp: Up to 2 years |
$1,500 sign-on bonus and New Hire Equity Grant for applicants that apply directly to ImmunityBio, payable in 90 days from start date, less applicable taxes and withholdings. POSITION: The Manufacturing Associate at ImmunityBio is responsible for supporting Biological Manufacturing. All functions and roles of the manufacturing process must be compliant with Current Good Manufacturing Processes (cGMP) and Good Documentation Processes (GDP) to ensure successful, quality operations. The Manufacturing Associate will participate in scale up and transfer of new products. | 6/9/2022 |
| 6675 | NantKWest Woburn, MA Research Associate Master’s degree in Biological Science Exp: 1+ year |
ImmunityBio is seeking a Research Associate for its Woburn, Massachusetts location. The successful candidate will work as part of the cellular innovation team of ImmunityBio to develop next generation products for adoptive cell therapy based on the NK-92 cell platform and other immune cell-derived biologics. The Research Associate will report into the Director, Research & Development, and work closely with several PhD Scientists under the direction of the Chief Scientific Officer. | 6/9/2022 |
| 6676 | NantKWest Culver City, CA Research Associate B.S. in biochemistry or in related scientific disciplines Exp: up to 2 years |
ImmunityBio Inc. is seeking a highly motivated, full-time research associate to join the Protein Science group to support the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate should have a bachelor’s degree with 1-2 years of wet-lab experiences, ability to manage multiple tasks in a timely manner, good written/verbal communication skills and have a willingness to work as part of the team. | 6/9/2022 |
| 6677 | Nexelis Laval, QC Associate Scientist Cell-Mediated Immunity College degree and/or University degree in Chemistry, Biochemistry, Immunology or another appropriate field. Exp: 1 year |
Nexelis keeps growing and we are looking for a dynamic Associate Scientist to help support our growth and join our Cell-Mediated Immunity department. The Associate Scientist is responsible for laboratory work and documentation based on their assignment within the laboratory. They ensure that analyses and assigned tasks are performed in a timely manner and in accordance with appropriate SOPs and Good Documentation Practices (GDP). If you join our team, you will have the chance to participate in the daily life of the most successful advanced testing service provider in the immunology field. Involved in more than 15 SARS-CoV-2 vaccine developments in partnership with multinational pharmaceutical companies, innovative biotechnology companies and prestigious NGOs such as Bill and Melinda Gates Foundation or CEPI, we also proudly serve the needs of our clients in fields such as Flu (universal and seasonal), meningitis, respiratory syncytial virus (RSV), chikungunya, malaria, or HPV and are growing an immune-oncology franchise. | 6/9/2022 |
| 6678 | Nexelis Laval, QC Associate Scientist, Virology DEC or Bachelor's degree in Immunology, Biochemistry, Biology or Microbiology or related scientific field, or equivalent Exp: 1 to 2 years |
Nexelis keeps growing and we are looking for enthusiastic Associate Scientists to join our Virology team. At Nexelis you will have the chance to participate in the daily life of the most successful advanced testing service provider in the immunology field. Involved in more than 15 SARS-CoV-2 vaccine developments in partnership with multinational pharmaceutical companies, innovative biotechnology companies and prestigious NGOs such as Bill and Melinda Gates Foundation or CEPI, we also proudly serve the needs of our clients in fields such as Flu (universal and seasonal), meningitis, respiratory syncytial virus, chikungunya, malaria, or HPV and are growing an immune-oncology franchise. | 6/9/2022 |
| 6679 | NKMax America [NKGEN Biotech] Santa Ana, CA Quality Control Analyst I Masters Degree in Chemistry, or Biological Sciences Exp: 0-3 years’ |
NKGen Biotech is seeking a Quality Control Analyst to perform analytical testing in a cGMP environment. | 6/9/2022 |
| 6680 | Scendea Bishop’s Stortford, UK Associate Consultant - Product Development & Regulatory Affairs BS Life Sciences Exp: 0 yrs |
Undertake the writing of clinical trial and regulatory related documents. Perform literature/data searches and collate/summarise. Manage project documentation within company systems. Assess and analyse scientific data. Provide support to colleagues within the Scendea team. | 06/09/22 |
| 6681 | Workforce Genetics Rockville, MD Study Manager - Biomarkers CRO BS Life Sciences Exp: 1-2 years |
Our Study Management team provides a professional yet personal approach to study management. Our study managers are qualified scientists with lab experience and excellent organizational and communication skills. Study managers are the main point of contact and is responsible for the complex task of keeping studies on track. We have carried out numerous studies worldwide, with a continued commitment to achieving the desired outcome of all studies according to study scope and within the given time constraints. Each study manager ensures frequent, high-quality scientific and customer service delivery via effective and efficient operations. | 5/31/2022 |
| 6682 | Genesis Therapeutics San Diego, CA Research Associate - Biochemistry and biophysics Bachelor’s or Master’s of Science in biochemistry, biophysics, biology, or a related field. Exp: 1-5+ years |
Our lab in San Diego is recruiting associate scientists with experience in cellular, biochemical or biophysical techniques. Specifically, we are seeking candidates to prosecute plate-based pharmacology, cell culture, enzymology, cell engineering and drug discovery experimental plans for our rapidly advancing pipeline. Education requirements include a bachelor’s or master’s of science with specific focus in one or more of the following disciplines: cell signaling, cell physiology, protein biochemistry, cancer biology and immunology. This is a full-time position in a fast-paced biotech environment with a collegial group of high level colleagues working towards well-defined goals. Full medical and dental benefits, flexible work hours/vacation included in this opportunity to learn all aspects of biotech start-up. | 5/31/2022 |
| 6683 | Genesis Therapeutics San Diego, CA Research Associate - Cell-based pharmacology bachelor’s or master’s of science in biology. Exp: 1-5+ years |
Our lab in San Diego is recruiting associate scientists with experience in cellular, biochemical or biophysical techniques. Specifically, we are seeking candidates to prosecute plate-based pharmacology, cell culture, enzymology, cell engineering and drug discovery experimental plans for our rapidly advancing pipeline. Education requirements include a bachelor’s or master’s of science with specific focus in one or more of the following disciplines: cell signaling, cell physiology, protein biochemistry, cancer biology and immunology. This is a full-time position in a fast-paced biotech environment with a collegial group of high level colleagues working towards well-defined goals. Full medical and dental benefits, flexible work hours/vacation included in this opportunity to learn all aspects of biotech start-up. | 5/31/2022 |
| 6684 | Genesis Therapeutics San Diego, CA Research Associate - Inhibitor mechanism of action Bachelor’s or Master’s of Science in related biological discipline. Exp: 1-5+ years |
Our lab in San Diego is recruiting associate scientists with experience in cellular, biochemical or biophysical techniques. Specifically, we are seeking candidates to prosecute plate-based pharmacology, cell culture, enzymology, cell engineering and drug discovery experimental plans for our rapidly advancing pipeline. Education requirements include a bachelor’s or master’s of science with specific focus in one or more of the following disciplines: cell signaling, cell physiology, protein biochemistry, cancer biology and immunology. This is a full-time position in a fast-paced biotech environment with a collegial group of high level colleagues working towards well-defined goals. Full medical and dental benefits, flexible work hours/vacation included in this opportunity to learn all aspects of biotech start-up. | 5/31/2022 |
| 6685 | IQVIA Durham, NC Associate Scientist Bachelor's Degree or equivalent combination of education and experience Exp: 6 months |
Responsible for performing routine analysis and laboratory testing procedures to obtain data for use in drug development and clinical trials research. | 5/31/2022 |
| 6686 | IQVIA Durham, NC Immunoassay Scientist Bachelor’s Degree in Chemistry or a related field Exp: 1 year |
Execution of ELISAs, RIAs, cell-based assays and other immunoassay techniques as required in a BSL2 lab under direction of project leader. Learn and perform required laboratory techniques using novel and established protocols and Standard Operation Procedures under the direction of project leader. Perform assays under direction of the project leader.Execution of ELISAs, RIAs, cell-based assays and other immunoassay techniques as required in a BSL2 lab under direction of project leader. | 5/31/2022 |
| 6687 | IQVIA Austin, TX Assay Development Associate Scientist Bachelor's Degree Bachelor's degree in relevant scientific discipline Required Exp: 1 year |
The Scientist for Assay Development contributes to the design of and is responsible for experiment execution of assay/method development. | 5/31/2022 |
| 6688 | Perrigo Allegan, MI Associate Scientist / Scientist - Analytical R&D Master's degree in Chemistry or Pharmaceutical Sciences Exp: 1-2 or more years |
The Professional in this role will be responsible for development of assay, impurities, dissolution, and physical characterization methods for oral and nasal drug products. There is an expectation of both direct hands-on laboratory work as well as mentoring/training of colleagues. This is a great career move for someone who wants to be involved in the entire drug product life cycle, participating from initial concept to commercial production, with opportunities to contribute to a successful global pharmaceutical business focused on Quality, Affordable Self-Care Products.The Professional in this role will be responsible for development of assay, impurities, dissolution, and physical characterization methods for oral and nasal drug products. There is an expectation of both direct hands-on laboratory work as well as mentoring/training of colleagues. | 5/31/2022 |
| 6689 | MEBTOX [LabCorp] Lincoln, NE Histotechnician/Histotechnologist - $5,000 Sign On Bonus requires a Bachelor's Degree Exp: 1-3 years |
LabCorp is seeking a Histotechnologist to join their Anatomic Pathology team in Lincoln, NE!; This position includes a $5,000 sign on bonus.; The schedule for this position is: Monday-Friday, 12:00pm to 8:00pmLabCorp is seeking a Histotechnologist to join their Anatomic Pathology team in Lincoln, NE! | 5/31/2022 |
| 6690 | MEBTOX [LabCorp] Lincoln, NE Histotechnician/Histotechnologist - $5,000 Sign On Bonus requires a Bachelor's Degree Exp: 1-3 years |
LabCorp is seeking a Histotechnologist to join their Anatomic Pathology team in Lincoln, NE!; This position includes a $5,000 sign on bonus; The schedule for this position is: Monday-Friday, 5:00am to 1:00pm; Rotating Saturday and on call shiftsLabCorp is seeking a Histotechnologist to join their Anatomic Pathology team in Lincoln, NE! | 5/31/2022 |
| 6691 | MEBTOX [LabCorp] Madison, WI Study Technician (Research Assistant) Dose Formulations - Great for recent grads! Life Sciences recent Grad Exp: Entry Level |
As part of the Madison, WI dose formulations study technician team, primarily using wet chemistry equipment and techniques, you will prepare formulations for research studies that are evaluating the safety and effectiveness of new drugs. Common duties include preparing laboratory reagents, vehicles, diets, solution/suspensions and capsules according to study protocols; Sign-on Bonus: $4,000 ($2,000 upon hire and $2,000 after 6 months); How you will be rewarded – Pay rate: $19 per hour plus shift differential | 5/31/2022 |
| 6692 | MEBTOX [LabCorp] Wilmette, IL Histotechnologist Bachelor's Degree and meet all licenses necessary for Histology Exp: 1-3 years |
We are seeking Histology Professionals to join the LabCorp team where we are dedicated to providing the highest quality medical laboratory services. Come work as a Histotechnologist in our Pathology laboratory located in Wilmette, IL alongside a highly trained staff with the latest technology. Our services are performed with the utmost care, expertise, integrity and respect for the patient. | 5/31/2022 |
| 6693 | MEBTOX [LabCorp] Wilmette, IL Histotechnologist Bachelor's Degree and meet all licenses necessary for Histology Exp: 1-3 years |
We are seeking Histology Professionals to join the LabCorp team where we are dedicated to providing the highest quality medical laboratory services. Come work as a Histotechnologist in our Pathology laboratory located in Wilmette, IL alongside a highly trained staff with the latest technology. Our services are performed with the utmost care, expertise, integrity and respect for the patient. | 6/1/2022 |
| 6694 | MEBTOX [LabCorp] Greenfield, IN Study Technician (Research Assistant) - Anatomic Pathology Bachelor’s Degree in Life Sciences, or Associate Degree in Histology, Laboratory Animals Technology or Veterinary Technology Exp: Entry Level |
Study Technician (Research Assistant) - Anatomic Pathology, We are seeking talented science majors in the fields of Biology, Physiology, Animal Science, Zoology, Neuroscience, Biochemistry, Genetics, Microbiology, Immunology and similar; majors to work as a Pathology Study Technician (Research Assistant) in Greenfield, IN; Sign-on Bonus: $4,000 ($2,000 upon hire and $2,000 after 6 months; external candidates only); Labcorp Drug Development's work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life-saving work and help improve patients' lives while growing your career. In this role, you will perform basic necropsy or histology tasks on a variety of laboratory animals in compliance with the appropriate Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs) and regulatory guidelines. You will also monitor animal health and welfare in compliance with the Animal Health and Welfare Act and help maintain facilities for Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC) compliance.Study Technician (Research Assistant) - Anatomic Pathology | 6/1/2022 |
| 6695 | Asimov Boston, MA Research Associate I, High-throughput Assays B.S or B.A. in Biological Engineering, Molecular Biology, or a related field. Exp: a year |
As a full-time Research Associate on the Foundry team, this person will contribute to developing new tools for genetic engineering as well as research projects to develop high-throughput screening workflows. Working closely with Asimov’s world-class synthetic biology and high-throughput experimentation teams, this person will bring experience working in mammalian tissue culture, synthetic biology, and/or high-throughput assays. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering. | 6/1/2022 |
| 6696 | Mojo Vision Saratoga, CA Entry Level Hardware Engineer B.S. in Electrical, Computer Science or Mechanical Engineering Exp: Entry Level |
We have multiple openings for experienced hardware engineers to help us build our wearable device. You will be part of a larger team designing and building complex systems using a combination of custom ASICs, FPGA, and other off-the-shelf components. You will be working with systems relevant to real-time video/graphics, signal processing, sensor fusion and wireless data communication. | 6/2/2022 |
| 6697 | Merck West Point, PA Scientist - High Throughput Analytics-Vaccines M.S Engineering, chemistry/biochemistry/ or related field Exp: 1+ years |
The Vaccine Analytical Research & Development department of our Research & Development Division is seeking applicants for a Scientist position available at its West Point, Pennsylvania research facility. The primary lab-based role of the successful candidate will be to accurately perform automated and robotic biochemical, immunoassay, and cell-based methods. The candidate must be able to independently troubleshoot technical issues, participate in day-to-day lab maintenance activities, maintain accurate records, and is responsible for timely communication of data. Additionally, the individual will be responsible for maintaining laboratory automation and robotic systems. The individual should have practical working knowledge of hardware and programming experience with robotic liquid handlers as well as scheduling software across a range of platforms (Tecan, Hamilton, HighResBiosoutions). The successful candidate must be able to solve complex analytical problems at the interface of biology, chemistry, and lab informatics, to enable development of vaccines supporting process development, formulation development, vaccine investigations and method lifecycle management. Lastly the individual will be expected to provide technical guidance related to method development, qualifications, validations, and transfers. This includes authoring reports, analytical protocols, qualification protocols, and technical reviewing data. The ideal candidate should bring expertise in a wide variety of automation and robotic methods with an emphasis, engineering, chemistry, and virology. The successful candidate must function well and be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. Applicants must have effective organizational, multi-tasking, oral/written communications skills, show scientific leadership, and a desire to conduct research. Evidence of cross-functional collaboration in an academic or industrial setting is also preferred. | 6/2/2022 |
| 6698 | Merck Boston, MA Biology Discovery Scientist M.S. in the area of immunology, cancer biology, or related area Exp: 0+ years |
We are seeking a highly qualified scientist with a strong background in Oncology/Immune-Oncology to join our Discovery Oncology team in Boston. The successful candidate will have a track record of multi-parameter immunophenotyping and mechanism of action studies. Primary responsibilities will include designing and carrying out experiments in the lab to support our pipeline projects. An ability to communicate clearly and collaborate effectively with colleagues in the discovery group as well as scientists from different disciplines will be essential. | 6/2/2022 |
| 6699 | Merck Boston, MA Protein Biology Discovery Scientist B.S. in biomedical sciences/engineering or related discipline Exp: 1-2 years |
Characterizing the binding affinity and kinetics profile is an essential component of discovering and progressing bio-therapeutic candidates in the discovery pipeline – Discovery Biologics/Protein Sciences Boston is looking for a scientist experienced in binding characterization method design and analysis. The qualified candidate will design and execute fit-for-purpose binding assays to characterize the binding activity, epitope specificity, cross reactivity, and quality of various bio-therapeutic candidates and protein reagents (including but not limited to antibodies, multi-specifics, Fc-fusions, immuno-cytokines, enzymes) across an array of technologies including Biacore, Octet, Microscale Thermophoresis (MST), KinExA, and ELISA. The successful candidate for this role will have a passion for hands-on science and overcoming challenges in assay development, be capable of managing multiple projects/workflows, and communicating/presenting findings to project team stakeholders. | 6/2/2022 |
| 6700 | Merck West Point, PA In Vitro Safety Pharmacology Scientist BS / BA degree/ MS degree Exp: BS: 1-5 years; MS: 1-2 years |
Conduct of manual and automated patch clamp assays under limited supervision (e.g., Molecular Devices’ pClamp11; Sophion’s Qpatch) Conduct of investigative in vitro models relevant to safety pharmacology under limited supervision (e.g., cardiomyocytes, neurons) | 6/2/2022 |
| 6701 | Merck Boston, MA Scientist, Molecular Discovery Bachelor’s degree in protein chemistry, biochemistry, engineering, life sciences or related discipline Exp: 1-3 years |
We are seeking an experienced and highly motivated scientist with a proven track record of analytical and biophysical characterization of diverse biologics molecules, including monoclonal antibodies, bi/multi-specifics and Fc-fusion proteins. The selected individual will fill a key role in the Discovery Biologics group at Our Company in Boston and be responsible for the detailed analytical characterization of early drug candidates using HPLC/UPLC based methods (SEC, RP, HIC), light scattering (SEC-MALS, DLS), thermal stability (DSF), capillary electrophoresis-based methods (CE-SDS) and mass spectrometry. Hands-on experience with high throughput method development, execution and data tracking is a plus. | 6/2/2022 |
| 6702 | Merck South San Francisco, CA Protein Characterization B.S. in biology or related science field Exp: one (1) year |
Develop, optimize, and carry out functional assays and protein characterization assays in various formats, Understanding of assay validation and statistical best practices, Ability to communicate results effectively, Well organized and able to track multiple efforts simultaneously, Willingness to work independently or as part of a group | 6/2/2022 |
| 6703 | PerkinElmer San Diego, CA Biochemist - Conjugation Bachelor of Science in Biology/Chemistry or related area Exp: less than 1 year |
The Biochemist I will be an integral member of a team, that manufactures and provides conjugated antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research; This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform troubleshooting of problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks.The Biochemist I will be an integral member of a team, that manufactures and provides conjugated antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. | 6/2/2022 |
| 6704 | PerkinElmer San Diego, CA Research Associate - Recombinant Protein & Molecular Cloning BS in biological sciences Exp: 1+ years |
This position is responsible for developing cutting edge recombinant protein research products in Molecular Cellular Biology group. The research associate will be involved on developing a new line of recombinant protein products by supporting other team members. The duties include preparing buffer solutions and cell culture media, performing PCR and DNA purification according to standard operating procedures, performing bacterial and mammalian cells cultures, and purifying recombinant proteins with affinity tag. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 6/2/2022 |
| 6705 | PerkinElmer San Diego, CA Research Associate I - Process Development (Antibody Conjugation) Bachelor’s Degree in Biology, Biochemistry, Chemistry, or related Science. Exp: 6 months |
The position is an important member of a team to pre-screen and optimize conditions for new product launch and for product transfer to manufacturing. The position works with antibodies and reagents for research areas including immunology, neuroscience, stem cells, and cell biology. This is a great opportunity to enhance your knowledge in a highly competitive biotechnology industry. BioLegend is a fast growing company and an industry leader who is committed the effort to provide top line quality products to our customers and the best tools for scientific community. This position is lab based and will work independently in a team setting to perform all essential functions that related to small scale antibody production, conjugation, and purification. It requires the ability to follow SOPs, complete batch records, and finish assignments in a timely manner. This position will also perform troubleshooting, and also responsible for assisting the supervisor with laboratory operations and completing production requirements before due dates. | 6/2/2022 |
| 6706 | PerkinElmer San Diego, CA Research Associate I -Diagnostics Bachelor’s degree in a Life Sciences-related field Exp: 1 years |
BioLegend is seeking a highly motivated Product Development Research Associate to join our Diagnostic Product Development Team. This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report. | 6/2/2022 |
| 6707 | PerkinElmer San Diego, CA Biochemist - Bacterial Cell Culture Bachelor of Science in Life Science or related area Exp: 1+ years |
This position is responsible for manufacturing cutting-edge recombinant protein research products in Molecular Cellular Immunology (MCI) group. The recombinant manufacturing associate will be involved in different stages of production of various recombinant protein products, which includes recombinant protein expression and purification. The duties include preparing buffer solutions and cell culture media, performing bacterial cultures, purifying recombinant proteins, and performing DNA isolation according to standard operating procedures. Another part of the job responsibility includes transferring the products to other groups for testing, preparing product/project-related documentation, and maintaining the inventory and record for recombinant protein products. | 6/2/2022 |
| 6708 | PerkinElmer Lafayette/ Denver, CO Associate Scientist Bachelor's Degree in Life Sciences (Biology, Chemistry, etc.) or a closely related field, required Exp: 0-3 years |
Horizon Discovery is an award-winning biotech company headquartered in Cambridge, UK with a global presence across the US, Europe and APAC regions. Using our proprietary gene-editing platform and deep scientific expertise, we design and engineer a diverse portfolio of inspired cell solutions to pharmaceutical, biotech, CRO, diagnostic, clinical laboratory and academic areas across the globe. Horizon has a rewarding and exciting opportunity for an enthusiastic Associate Scientist for our Synthetic Manufacturing laboratory. Key responsibilities include a wide array of duties related to the manufacturing, processing, and packaging of RNA and DNA oligonucleotides. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry in multiple laboratories. | 6/2/2022 |
| 6709 | Sanofi Framingham, MA Research Associate Bioprocess Analytics Bachelor’s degree in Analytical Chemistry, Biochemistry or related discipline Exp: Entry Level |
This position resides within the BioProcess Analytics group which is part of the Global Biologics CMC Development organization at Sanofi, Framingham, MA. The candidate will be part of a multi-disciplinary team providing analytical support to a strong pipeline of R&D programs within Sanofi during early and late stage process development. We are looking for a skilled, highly motivated individual with expertise in chemistry/biochemistry who works well in a team-setting to meet project and development goals within established timelines. The Research Associate will be part of a multi-disciplinary team focused on multiple projects to support development and optimization of novel analytical methods, including routine testing, for R&D programs within Sanofi. This entry level position will offer the ideal candidate the opportunity to explore and grow their skills in several analytical disciplines while working with cutting-edge technologies and methodologies. | 6/2/2022 |
| 6710 | Sanofi Waltham, MA mRNA, Research Associate II/Senior Research Associate-Plasmid Production M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology) M.S. in a related field (e.g., Chemical En Exp: 1-3 years |
As an experienced molecular biologist, you will be responsible for production a wide range of plasmid constructs with high quality and reproducibility, independently work on plasmid design, construction, purification, characterization. | 6/2/2022 |
| 6711 | Sanofi Waltham, MA Associate Scientist Research B.S./M.S in Immunology/Cell Biology/Biochemistry or related field Exp: BS: 1-4 years; MS: 0-2 years |
The Complement-mediated disorders research cluster in the Immunology and Inflammation therapeutic area within Sanofi is seeking an experienced and highly motivated scientist with experience in immunology to join their growing team. A successful candidate will contribute to both characterization of disease state and discovery of novel candidate drugs, including the design and execution of proof of concept and validation assays. He/she will support projects from discovery research into early development as an active member of cross-functional teams. The candidate must be driven, resourceful, and able to work independently. Excellent organizational skills in management of data, reagents and equipment are essential. The candidate will participate in regular team meetings and present results, interpret data, and formulate conclusions. Teamwork, collaboration with colleagues across disciplines and excellent verbal and written communication skills are critical | 6/2/2022 |
| 6712 | Sanofi Framingham, MA Research Associate Cellular Therapies Bioanalytics Bachelor's degree in biological sciences or related discipline Exp: 1 – 3 years |
The Research Associate is responsible for executing test methods under control of established procedures. Specifically, performing in-process and release testing of cellular therapies out of our 45 NYA manufacturing facility. Additional functions will include interpretation of data, preparation of test documentation, and management of analytical databases. We are looking for a candidate that is capable of learning quickly with the goal of executing analytical methods and managing assigned test schedules, with excellent communication skills. The position is primarily located in Framingham, MA but will be moving to Waltham, MA in August, 2022. | 6/2/2022 |
| 6713 | Sanofi Waltham, MA mRNA, Research Associate, Synthetic Chemistry - Vaccine Waltham, Massachusetts B.S or M.S in organic chemistry Exp: 1-3+ years |
We are looking for a highly motivated and enthusiastic Associate Scientist to join our chemistry team at the Sanofi mRNA Center of Excellence (CoE). This position reports to Senior Scientist, Chemistry, Research, and Biomarker, in the mRNA Center of Excellent (CoE) at Sanofi and is based in Waltham, Massachusetts. As part of our integrated lipid chemistry team, this position has the responsibility to conduct synthesis, purification, and structural characterization of novel lipids from milligrams to multi-grams effectively and safely. This position also has the responsibility of exploring and deploying innovative synthetic methods for various lipid syntheses to support mRNA-LNP vaccine delivery. This is an excellent opportunity for individuals who are eager to gain knowledge and learn cutting-edge technology in organic synthesis, medicinal chemistry, drug delivery, immunology, and novel vaccine discovery and development. | 6/2/2022 |
| 6714 | Sanofi Waltham, MA mRNA - Analytical Development Research Associate - Vaccine BS in analytical chemistry, biochemistry, or biotechnology or equivalence Exp: 0-2 years |
As an mRNA Research Associate Scientist in Analytical Sciences, you will ensure laboratory activities in support of process development and industrialization and ensure the characterizations of mRNA vaccines in development. | 6/2/2022 |
| 6715 | Siemens Healthineers Walpole, MA Biochemist 1 - Reagent Manufacturing BS/BA in related discipline, or advanced degree, where required Exp: 0-2 years |
We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as a Biochemist 1 – Reagent Manufacturing. The primary roles of this individual are to provide Technician support in the Reagents work center as well as ensuring that the schedule is made and executed. They will provide updates on ongoing builds. Candidate must demonstrate ability to understand formulation processes; work with processes and equipment; detailed written documentation of work; ability to work well with others. | 6/2/2022 |
| 6716 | Siemens Healthineers Walpole, MA Biochemist 1 - Reagent Manufacturing 2nd Shift BS/BA in related discipline, or advanced degree, where required Exp: 0-2 years |
The primary roles of this individual are to provide Technician support in the Reagents work center as well as ensuring that the schedule is made and executed. They will provide updates on ongoing builds. Candidate must demonstrate ability to understand formulation processes; work with processes and equipment; detailed written documentation of work; ability to work well with others. | 6/2/2022 |
| 6717 | Siemens Healthineers Walpole, MA QC Microbiology Lab Technician I - Tuesday - Saturday after training Bachelor’s Degree in life sciences or equivalent work experience required. Exp: 0-1 years’ |
We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as a QC Microbiology Technician 1 – 1st Shift Tuesday through Saturday (after training). | 6/2/2022 |
| 6718 | Siemens Healthineers Walpole, MA Biochemist I BS in Biology, Chemistry, Biochemistry, Immunology, or other related sciences Exp: 1+ years |
We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as a Biochemist. This Biochemist position supports the manufacture of laboratory diagnostic assays that are used by clinical labs around the world. Your work will impact clinical decisions and patient outcomes for infectious diseases, oncology, and other disease states. Join us for an exciting opportunity to grow and develop your passion for science, cutting-edge technology, and improving patient care globally. | 6/2/2022 |
| 6719 | Siemens Healthineers Walpole, MA Biochemists - 2022 Life Science College Graduates BS in Biology, Immunology, Virology, Chemistry, Biochemistry, Biotechnology or other related Life Science fields Exp: 1-3 years |
Join our team now at Siemens Healthineers as a Biochemist 1. Positions will be located in one of the following areas: Technical Operations or Reagent Manufacturing. Our Biochemist 1 – Reagent Technical Operations positions are responsible for participating in and investigating technical issues related to the formulation and testing of immunoassay reagents and testing components. Individuals will create and participate in the Design of Experiments to troubleshoot manufacturing issues and effectively communicate your data both verbally and written with other departments such as Quality Control, Quality Assurance, Engineering, Manufacturing, and R&D. Individuals will also operate the Atellica IM, ADVIA Centaur and ADVIA CP and other instruments in a laboratory setting. In addition, individuals will serve as the technical lead for projects related to material/formulation changes, manufacturing process changes, productivity savings, and specification changes Our Biochemist 1 – Reagent Manufacturing positions are responsible for auditing Manufacturing documentation including Manufacturing Batch Records, Bills of Materials, Routings, Process Documents and SOP’s. Additional duties include working with Manufacturing Supervisor to coordinate and monitor day to day assignments of a group of Manufacturing Technicians, as well as providing training to qualify technicians for manufacturing activities. Individuals will also participate in identifying and initiates continuous improvement activities. These positions involve the handling of all types of materials, including but not limited to hazardous and DEA (Drug Enforcement Agency) controlled materials. | 6/2/2022 |
| 6720 | Siemens Healthineers Walpole, MA Biochemist 1 - Reagent Manufacturing - Precommercial Support BS/BA in related discipline, or advanced degree, where required Exp: 0-2 years |
The Reagent New Product Biochemist 1 position will cover Laboratory Diagnostics Commercial Manufacturing and Pre-Commercial builds. Reporting to the Manufacturing Supervisor, the primary functions of this individual are to; Manufacture Reagents Material (Wetcakes, Lite Reagents, Solid Phases, Ancillary Reagents) for new product development, provide feedback on manufacturing work instructions as they mature through development, and to represent Reagents Manufacturing as a Subject Matter Expert (SME) in cross-functional team meetings such as pFMEAs, Process Reviews, and Element Team meetings. | 6/2/2022 |
| 6721 | Jordi Labs Mansfield, MA Chemist Master’s degree in chemistry or other closely related field Exp: one year |
Job duties: 1) Prepare technical reports 2) Interpret gas chromatograph mass spectrometry (GCMS) and liquid chromatograph mass spectrometry (LCMS) results with a high level of proficiency 3) Interpret chromatographic data including high performance liquid chromatography (HPLC), gas chromatography (GC), and gel permeation chromatography (GPC) results 4) Combine results from multiple techniques to identify unknown chemical compounds 5) Quantify chemical components using HPLC and GC results 6) Work with a team of scientists to design and implement analytical strategies 7) Perform or oversee complex analytical strategies with an emphasis of MS and chromatography 8) Review technical reports written by other scientists | 6/2/2022 |
| 6722 | Gritstone Oncology Cambridge, MA RESEARCH ASSOCIATE, EPITOPE & TCR DISCOVERY BS/BA degree Exp: 0-2 years |
Gritstone bio is seeking a research associate to help discover novel T cell targets and TCRs for multiple infectious disease and oncology programs. The primary role of the research associate is to collaborate within and across teams to further develop and optimize a high-throughput discovery platforms to drive the therapeutic program and support key company initiatives. Approaches cover the broad spectrum of molecular/cell biology and immunology and include flow cytometry and cell sorting, T cell cultures, nucleic acid extraction and PCR and DNA/RNA library construction. We are looking for an enthusiastic and adaptable team player who will thrive in a fast-paced dynamic and highly collaborative environment. This is an opportunity to work for a well-funded biotechnology company driving innovative infectious disease and oncology programs. | 5/24/2022 |
| 6723 | Gritstone Oncology Emeryville, CA RESEARCH ASSOCIATE II, TRANSLATIONAL IMMUNOLOGY MS in Immunology, Infectious Disease, Cell Biology, or other related scientific discipline Exp: 1+ year’s |
Gritstone bio is seeking a Research Associate who will leverage their skills in assay design, development, qualification, sample testing, and data analysis to support the advancement of our infectious disease and oncology pipelines. The RA will join our Emeryville-based Immunology Assay group, as part of the Translational Immunology team, to perform developed and exploratory assays on preclinical samples in collaboration with scientists across the Research organization. | 5/24/2022 |
| 6724 | Gritstone Oncology Cambridge, MA RESEARCH ASSOCIATE II, MASS SPECTROMETRY Bachelor’s degree (or equivalent), preferably in scientific discipline or a health-related field. Exp: 1+ years |
The Mass Spectrometry and Proteomics group at Gritstone bio is looking for a Research Associate II to manage mass spectrometry instrumentation and perform wet lab experiments to support the HLA-immunopeptidomics platform. The ideal candidate will be actively engaged in processing and preparing samples prior to mass spectrometry analysis to build and expand our tumor HLA peptide dataset and to enable target discovery for novel cancer immunotherapies. We are looking for an enthusiastic and flexible team player who will thrive in a fast-paced, dynamic, and highly collaborative environment. This is an opportunity to work for a well-funded, public biotechnology company driving personalized cancer treatments.The Mass Spectrometry and Proteomics group at Gritstone bio is looking for a Research Associate II to manage mass spectrometry instrumentation and perform wet lab experiments to support the HLA-immunopeptidomics platform. The ideal candidate will be actively engaged in processing and preparing samples prior to mass spectrometry analysis to build and expand our tumor HLA peptide dataset and to enable target discovery for novel cancer immunotherapies. | 5/24/2022 |
| 6725 | High Purity New England Smithfield, RI Automation Control Engineer Bachelor’s degree in engineering preferred Exp: 1-3 years |
In this key role, the Automation Control Engineer will assess a problem and design a new system or improve the existing one to make it better and more efficient. This position will demonstrate technical competency, deliver mission-critical infrastructure, and ensure the highest quality and peak performance for HPNE products and services. | 5/24/2022 |
| 6726 | Ifyber Ithaca, NY Laboratory Technician BS degree Exp: 1 year |
The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. | 5/24/2022 |
| 6727 | IGM Biosciences Mountain View, CA Research Associate I / II / III BS or higher degree in Cell Biology, Biochemistry, or related scientific discipline. Exp: 1 – 3 years |
We are looking for a Research Associate with a background in Cell Biology or Biochemistry to join our growing and friendly team during this exciting time in our expansion. You will play an integral role in the antibody discovery and validation for the development of novel immuno-oncology therapeutics. In this position, you will perform protein characterizations and cell-based immunoassays, think creatively to solve problems, constantly improve work practices, and work productively as part of a team. | 5/25/2022 |
| 6728 | IGM Biosciences Mountain View, CA Research Associate I / II / III BS, MS, or PhD in Pharmacology, Immunology, Cell Biology or related scientific discipline. Exp: RA I: BS 0+ years; RA II: MS with 0+ years |
We are looking for a Research Associate with a background in Pharmacology, Immuno-oncology, or Immunology to join our growing and friendly team during this exciting time in our expansion. You will play an integral role in the pre-clinical development of novel immuno-oncology therapeutics. In this position, you will perform standard cell-based functional assays and immunoassays, in vitro and in vivo studies, think laterally to solve problems, constantly improve work practices, and work productively as part of a team. | 5/25/2022 |
| 6729 | Immuneering San Diego, CA Research Associate, Translational B.S. or M.S. in a scientific discipline. Exp: 1-3+ years |
We have an immediate opening for a full-time Research Associate. The ideal candidate is quality and process-oriented, flexible and must enjoy the challenges of working in a fast-paced, start-up biotechnology company with diverse people and drug programs. The Research Associate is responsible for performing research and development experiments for projects and products in collaboration with others. Regularly exercises technical discretion in the design, execution and interpretation of experiments that contribute to project goals. Contributes to project process within scientific discipline through innovative research. | 5/25/2022 |
| 6730 | Immuneering San Diego, CA IT System Engineer Bachelor’s degree in computer science, or information technology Exp: 1+ years |
At Immuneering, cloud computing continues to allow us to modernize and consolidate IT infrastructure, automate workloads, and pursue next-generation scientific innovation. To continue this transformation, we’re seeking a cloud engineer with expertise in the strategy, design, development, and implementation of projects in the cloud. The ideal candidate is experienced in cloud-based technology such as AWS, Azure and SaaS, with a firm grasp of emerging technologies. From day one, you’ll have an immediate impact on the day-to-day efficiency of our IT operations, and an ongoing impact on our overall growth. This position will be based at our San Diego office where hands on support to the laboratory staff is a requirement. | 5/25/2022 |
| 6731 | ImmuneID Waltham, MA Research Associate/Senior Research Associate - Immunology Bachelor’s degree in biology, biochemistry, or a relevant life sciences discipline Exp: 0-2 years |
ImmuneID aims to revolutionize therapeutic drug development by fingerprinting immune disease drivers. We are looking for an experienced, motivated Research Associate to join our growing team of passionate researchers focused on unlocking human immunology. Our dynamic and innovative culture favors highly organized candidates, eager to learn and confident to work across boundaries. As a member of the Immunology team, the Research Associate will provide support in developing and running experiments to understand the biology of autoimmune diseases and therapies. They will work closely with Scientists to address the day-to-day needs of ImmuneID’s laboratory environment in a timely manner, maximizing research productivity and efficiency. This role will be afforded numerous opportunities for professional and career development in biotech startup laboratory research. | 5/25/2022 |
| 6732 | Imperative Care Campbell, CA R&D Engineer Bachelor’s degree in Engineering: mechanical, biomedical, or similar preferred Exp: 0-5 years |
This position is responsible for the late-stage design development through high volume manufacturing of market-released neuro-interventional medical devices such as catheters, guidewires, etc. They will assist in creative problem solving supporting the launch and scaling of innovative products by recognizing areas for improvement and transforming ideas into actionable solutions. Responsibilities will include, but not limited to, failure analysis, design changes and documentation, test method development, requirement and specification development and testing and data analysis. | 5/25/2022 |
| 6733 | InBios International Seattle, WA Manufacturing Associate I - Rapid Spray Bachelor’s degree in life sciences or a similar field Exp: 1 year |
We would like to see your resume if you have general laboratory experience and a willingness to learn more lab skills. You enjoy working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale lateral flow diagnostic test components. You have a personality that is easily adaptable to changing priorities and are eager to work alongside a dedicated team that consistently meets deadlines and delivers products that meet high quality standards. If you are seeking an entry-level position with short-term and long-term prospects at the forefront of medical diagnostic biotechnology this is a great opportunity for you | 5/25/2022 |
| 6734 | InBios International Seattle, WA Manufacturing Associate I- ELISA Bachelor’s degree with emphasis on life science Exp: 0-1+ years |
We would like to see your resume if you have received a degree with an emphasis on life sciences. If you have work experience in a GMP/ISO 13485 manufacturing facility and/or you have experience with PCR test-kit manufacturing please be sure to include that information on your resume or in a cover letter. If you would like to be part of a team responsible for the production of large-scale ELISA diagnostic test components in a BSL-2 laboratory, and you enjoy a busy workday under general supervision with daily goals working alongside a dedicated team that consistently meets deadlines and delivers products that meet high quality standards, then we encourage you to apply for this position. | 5/25/2022 |
| 6735 | InBios International Seattle, WA Manufacturing Engineer I Bachelor's degree (BS) in mechanical or electrical engineering Exp: 0-1+ years |
Self-driven with proven ability to successfully manage a broad range of tasks, including optimizing process performance, troubleshooting quality and equipment issues, authoring technical documents. If you enjoy technical challenges in a fast-moving environment, then we encourage you to apply for this position. | 5/25/2022 |
| 6736 | InBios International Seattle, WA Quality Assurance Associate II Thesis-based MS Degree in engineering or life sciences. Exp: 1+ years |
We are seeking a mindful and diligent individual with a warm and welcoming attitude who has excellent organizational and communication skills and a keen eye for detail. If you enjoy analytical work, leading and collaborating on projects, a variety of responsibilities, and being part of a reliable and dedicated Quality Assurance team, then we encourage you to apply for this position. | 5/25/2022 |
| 6737 | InBios International Seattle, WA Quality Control Assistant - Biotech BS in Chemistry, Biology, Bioengineering, or other relevant discipline. Exp: 0 – 1 year |
You have a degree in chemistry, biology, bioengineering or related life science field of study and are looking for an entry level QC position and an opportunity to learn and grow your skills and career. You thrive in a busy and structured work environment working with a team of Quality Control Associates under the supervision of the Quality Control Manager. You are thorough and able to see and report details and variances as well as able to follow and adhere to established procedures and protocols. You are a reliable worker who is comfortable working and contributing to team demands and goals. | 5/25/2022 |
| 6738 | InBios International Seattle, WA Research Associate I/II - ELISA R&D Bachelor’s degree in a biological or related life sciences, such as Immunology, Microbiology or Biochemistry Exp: 0-2 years |
You have a biologicals, life sciences degree, good antibody and antigen knowledge, with little to no professional immunoassay development experience. You thrive in a fast-paced work environment where priorities and projects may change quickly. You are attentive and still eager to learn as you continue to hone your already acquired knowledge and skills under the supervision and instruction of the team’s lead scientist. You have proven yourself to be a teammate who is responsible and motivated and comfortable working closely in a team environment, where you openly share ideas and collaborate. | 5/25/2022 |
| 6739 | Insmed San Diego, CA Research Associate Gene Therapy Bachelors’ degree in biology, chemistry, or related field. Graduate degree holders are encouraged to apply. Exp: 0-1+ years |
Insmed is seeking a Senior Research Associate Gene Therapy. Depending on experience, the scientist will expand molecular and product specific assay development working with the analytical development team. General cellular and molecular biology proficiency is advantageous to the company. Skills such as western blot, cloning, general mammalian cell culture and transfection will be considered advantageous. | 5/25/2022 |
| 6740 | Instil Bio Dallas, TX Research Associate/Senior Research Associate, US Research MS Degree Exp: 1+ years |
We are seeking a highly motivated individual to join the research team to participate in Instil Bio’s discovery efforts and play a pivotal role in advancing key TIL engineering programs. The successful candidate be part of a research team focused on advancing current programs and developing new internal technology assets with the ultimate goal of developing cell therapy IND candidates for the treatment of solid tumors. In this role, the candidate will be directly reporting to a Scientist or Senior Scientist in Research. | 5/25/2022 |
| 6741 | Pace Analytical Naperville, IL Lab Technician Bachelor's degree in chemistry, chemical engineering, biochemistry. Exp: 0-2 years |
The laboratory technician supports and conducts testing under the supervision of senior researcher(s). We are is seeking a candidate who can work independently conducting day to day test work. The senior researcher(s) will direct their work, but it's up to the candidate to manage experimental execution and reporting. Note: This position is expected to last 1 year. The laboratory technician supports and conducts testing under the supervision of senior researcher(s). We are is seeking a candidate who can work independently conducting day to day test work. The senior researcher(s) will direct their work, but it's up to the candidate to manage experimental execution and reporting. Note: This position is expected to last 1 year. | 5/25/2022 |
| 6742 | Pace Analytical Greenfield, IN Biologist Bachelor's degree in Biology Exp: 0 - 1+ years |
Candidate will use their skills and knowledge in Biology/Microbiology to support development of new products. | 5/25/2022 |
| 6743 | Pace Analytical Naperville, IL Lab Technician B.S./B.A degree in Chemistry, Biochemistry, or related field Exp: 0 - 1+ years |
Looking for a Lab Technician to join the Organic Synthesis (Polymer) Lab. The lab technician performs a variety of routine laboratory operations with technical direction from a supervisor. Note: This position is expected to last 1 year. Looking for a Lab Technician to join the Organic Synthesis (Polymer) Lab. The lab technician performs a variety of routine laboratory operations with technical direction from a supervisor. Note: This position is expected to last 1 year. | 5/25/2022 |
| 6744 | Pace Analytical Maplewood, MN Quality Analyst Bachelor’s degree in Chemistry or Biochemistry Exp: 0-2 years |
This candidate will actively support the quality and production team with hands on lab work and data analysis for sterilization assurance products. The products being developed are crucial to sterilization of medical instruments within the healthcare industry. Work is performed independently in a shared lab environment | 5/25/2022 |
| 6745 | Pace Analytical Maplewood, MN Lab Analyst - Microbiology BS degree in Biological science or related field Exp: 1-3 years |
This position will actively support food safety and quality assurance through the use, and validation of, pathogen detection products. The analyst will prepare and evaluate samples using aseptic technique to ensure products meet specifications. The products being monitored are crucial to maintaining consumer safe food supply chains. Work is performed as part of a team in a collaborative environment. | 5/25/2022 |
| 6746 | Pace Analytical Eagan, MN Lab Technician Bachelors degree in the area of chemistry, chemical engineer or science preferred Exp: 0-2 years |
The main function of a chemical technician is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. A typical chemical technician is either a research technician that works in an experimental lab or a process control technician who works in a manufacturing setting. The research technician works on research and development and collects samples or produces compounds. The process control technician focuses on quality assurance and production processes. NOTE: This position is expected to last 12 MonthsThe main function of a chemical technician is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. A typical chemical technician is either a research technician that works in an experimental lab or a process control technician who works in a manufacturing setting. The research technician works on research and development and collects samples or produces compounds. The process control technician focuses on quality assurance and production processes. NOTE: This position is expected to last 12 Months | 5/25/2022 |
| 6747 | Invicro Needham, MA Laboratory Assistant, Advanced Pathology Services Bachelor’s degree in a relevant biological science. Exp: 1-2 years’ |
Work as part of Lab Services team to provide support for all routine Histology and IHC work pertaining to delivery of CAP/CLIA and GLP-like oriented lab services offered to external partners, including BioPharma, Academia, and Oncology Research Centers. | 5/25/2022 |
| 6748 | Invivo Biosystems Eugene, OR Computational Biologist I Bachelor's degree in computer science, bioinformatics (or related discipline) and/or biological sciences Exp: up to 2 years |
Join our team that provides in-vivo analytical services, produces data and insights for companies that need to make go/no-go decisions quickly, and advances the discovery and early-stage development of new compounds. The Computational Biologist I is a critical component in helping our clients further their research goals. You will be instrumental in supporting how we acquire, aggregate, and analyze phenotype data from model organisms. Collaborating with our team and our customers, you will work on a variety of challenging projects to advance scientific discovery. The ideal candidate will be able to perform self directed exploration and analysis of complex datasets, in addition to analyses under the direction of supervisors.Join our team that provides in-vivo analytical services, produces data and insights for companies that need to make go/no-go decisions quickly, and advances the discovery and early-stage development of new compounds. The Computational Biologist I is a critical component in helping our clients further their research goals. You will be instrumental in supporting how we acquire, aggregate, and analyze phenotype data from model organisms. Collaborating with our team and our customers, you will work on a variety of challenging projects to advance scientific discovery. The ideal candidate will be able to perform self directed exploration and analysis of complex datasets, in addition to analyses under the direction of supervisors. | 5/25/2022 |
| 6749 | Invivoscribe San Diego, CA Manufacturing Associate I B.S. Degree in a scientific discipline, preferred. Exp: 1+ years |
We are looking to add a Manufacturing Associate I to our team for all aspects of production, including the production of master mixes and controls. You will contribute to the drafting and review of new documents, including SOPs, Batch Records and Purchasing Specifications. | 5/25/2022 |
| 6750 | Charles River Laboratories Shrewsbury, MA Research Technician 1 Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months to 1 year |
Performs technical tasks in the conduct of in vivo research studies or support services in accordance with good animal welfare practices. Prepares, collects and records research data and specimens in compliance with applicable regulations and SOPs. We are seeking an expereienced Research Technician I for our InVivo (InLife) Team within our Safety Assessment site located in Shrewsbury, MA. The following are responsibilities related to the Research Technician 1: The Research Technician 1 will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.Performs technical tasks in the conduct of in vivo research studies or support services in accordance with good animal welfare practices. Prepares, collects and records research data and specimens in compliance with applicable regulations and SOPs. We are seeking an expereienced Research Technician I for our InVivo (InLife) Team within our Safety Assessment site located in Shrewsbury, MA. The following are responsibilities related to the Research Technician 1: The Research Technician 1 will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 5/25/2022 |
| 6751 | Charles River Laboratories Cambridge, MA Research Study Technician 1 Bachelor's (B.A./B.S.) Degree preferred. Exp: (6-12) months |
We are seeking a Research Study Technician 1 for our Insourcing Solutions Department located in Cambridge, MA. Observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations.We are seeking a Research Study Technician 1 for our Insourcing Solutions Department located in Cambridge, MA. Observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. | 5/25/2022 |
| 6752 | Charles River Laboratories Carlsbad, CA Research Associate - $1000 SignOn bonus Bachelor’s degree in Life Sciences or related discipline Exp: 0 - 1+ years |
We are seeking a Research Associate for our Insourcing Solutions site located in Carlsbad. This position is offer a $1000 Signing Bonus!! The following are responsibilities related to the Research Associate: Performs technical tasks in the conduct of in vivo research studies or support services in accordance with good animal welfare practices. Prepares, collects and records research data and specimens in compliance with applicable regulations and SOPs.We are seeking a Research Associate for our Insourcing Solutions site located in Carlsbad. This position is offer a $1000 Signing Bonus!! The following are responsibilities related to the Research Associate: Performs technical tasks in the conduct of in vivo research studies or support services in accordance with good animal welfare practices. Prepares, collects and records research data and specimens in compliance with applicable regulations and SOPs. | 5/25/2022 |
| 6753 | Charles River Laboratories Cambridge, MA Research Study Technician 2 -$2K sign-on bonus Bachelor's (B.A./B.S.) Degree in animal or laboratory science or related discipline preferred. Exp: (1-2) years |
We are seeking an Research Study Technician 2 for our Insourcing Solutions Department located in Cambridge, MA. - Position includes a $2,000 sign on bonus. Observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in mice & rats for multiple clients. Maintain and monitor the health and physical environment of animals in research studies. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations | 5/25/2022 |
| 6754 | Charles River Laboratories S. San Francisco, CA Research Associate, Bioanalytical 1 Bachelor's degree (B.S./B.A.) or equivalent in a scientifically related discipline. Exp: Minimum 6 months |
We are seeking a Discovery Bioanalytical Research Associate (DMPK Bioanalytical) for our Discovery site located in South San Francisco, CA. We are seeking Research Associate candidates that are early in their careers and are highly motivated, enthusiastic and possess a passion for learning. This position will be involved in all aspects of studies supporting the bioanalysis of drug molecules in multiple matrices. This position is ideally suited to recent graduates who enjoy a fast-paced and collegial environment. The individual in this position will be responsible for working hands-on and under the direction of more senior staff in a dynamic environment where teamwork, data quality, innovation and speed are valued. | 5/25/2022 |
| 6755 | Charles River Laboratories Ashland, OH Research Assistant 1 (Bioanalytical Chemistry) Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required. Exp: Zero to two years |
We are seeking a Research Assistant I for our Safety Assessment Group site located in Ashland, Ohio. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples, and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. | 5/25/2022 |
| 6756 | Charles River Laboratories Mattawan, MI Research Analyst I - Analytical Chemistry Bachelor’s degree (BA/BS) Exp: No previous work experience required |
The Research Analyst 1 is responsible for the analysis of dose formulations according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. The team develops and validates methods using a variety of instruments and platforms, with an emphasis on ultra high performance liquid chromatography. The team assures that mixtures of test article with carrier are prepared at the proper concentration, are homogeneous, and are stable. In addition, the team is often involved in investigations and issues that are related to formulations and chemicals used on study. | 5/25/2022 |
| 6757 | Leica Biosystems Cortland, NY Associate Scientist Bachelor’s degree Chemistry, Chemical Engineering, Materials Science Exp: 1-3 years |
The Associate Scientist or Engineer provides performance data to R&D, Marketing, Sales and Quality that enable their ability to serve our customers in the Microelectronics industry. They are part of a dynamic team that develops and standardizes new test methods that allows us to characterize our materials and products in ways that as closely as possible mimics their end-use. | 5/25/2022 |
| 6758 | Leica Biosystems Madison, WI Associate Scientist II - Downstream Biomanufacturing B.S. in biochemistry, biotechnology, biology or related field Exp: 0-2 years |
The Associate Scientist II, Biomanufacturing is responsible for duties relating to standard purification of antibodies and proteins. | 5/25/2022 |
| 6759 | Leica Biosystems Ann Arbor, MI Research Scientist II Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field) Exp: one or more years |
The Research Scientist II, with supervision, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with development and characterization of new IDT genomics products in the NGS field. This position is involves independent research and R&D collaboration activities as well. This position is located in Ann Arbor, MI | 5/26/2022 |
| 6760 | Leica Biosystems Coralville, IA Research Scientist II - Verification and Validation Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field) Exp: one or more years |
The Research Scientist II, under minimal supervision, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with the development and characterization of new IDT genomics products in NGS, qPCR and functional genomics. This position is responsible for planning and executing experiments, analyzing data and reporting/presenting findings as well as supporting IDT customers. This individual will aid in the development and characterization of new genomics products in NGS and qPCR to help create cutting edge, robust new products, and assays for basic research, agricultural, and clinical applications. The preferred candidate will have previous bench level experience a research or industry setting and strong knowledge in basic laboratory and molecular biology techniques. Background in next-generation sequencing and/or qPCR are a plus | 5/26/2022 |
| 6761 | Leica Biosystems Newark, CA Quality Assurance Engineer Master's degree in engineering, technology, or science Exp: 0-2 years’ |
Support manufacturing and complaint handling/field sustaining leading to improved compliance with corporate policies, 21CFR820, ISO 13485, the Medical Device Directive, and other applicable regulatory agencies, while striving for continuous improvement. | 5/26/2022 |
| 6762 | Biodesix Boulder, CO Research Associate BS in Chemistry, Molecular Biology, Biochemistry, or related Exp: 0+ years |
This full-time position will have primary responsibilities to plan and execute projects in the Product Development team. Projects will include transfer of product concepts from the internal research team or external technology partners, development of concepts to transfer and launch implementation in collaboration with our Laboratory Operations team. | 5/18/2022 |
| 6763 | Biomérieux / BioFireBiomérieux / BioFireBiomérieux / BioFire Salt Lake City, UT Software Test Engineer I BS in Engineering or Science Exp: 0+ years |
We are looking for a talented and engaged Software Test Engineer to help ensure the quality of our product software applications. The successful candidate will work with a project team to scope, design, develop and test software applications used within BioFire. | 5/18/2022 |
| 6764 | Biomérieux / BioFireBiomérieux / BioFireBiomérieux / BioFire Salt Lake City, UT Manufacturing Engineer I - Weekend Day Shift BS in Engineering or related Exp: 0+ years |
This engineer works on a cross-functional Manufacturing Engineering team to support a limited aspect of the consumable manufacturing process. Partners with internal team members to optimize product performance. Performs troubleshooting and routine maintenance of basic manual and automated manufacturing processes under supervision of senior engineers and management. | 5/18/2022 |
| 6765 | Biomérieux / BioFireBiomérieux / BioFireBiomérieux / BioFire St. Louis, MO Lab Technician: Media Lab, 3rd Shift BS in Chemistry, Biology, or related Exp: 1+ years |
The primary purpose of this position is to prepare complex chemical media and/or sub components, dispensing system setup/verifications, insuring timely delivery of high quality product to Card production, being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 5/18/2022 |
| 6766 | Biomérieux / BioFireBiomérieux / BioFireBiomérieux / BioFire Philadelphia, PA Associate Scientist BS in Biological Sciences Exp: 0-4 years |
All work is performed in a food safety laboratory testing for the presence of common pathogens such as Salmonella and Listeria as well as other food spoilage organisms. Technologies used in the laboratory include traditional microbiology, PCR/qPCR, mass spec and advanced microbiology methods such as TEMPO. The Associate Scientist performs all work in accordance with ISO/IEC 17025:2017 standards. This position requires meticulous record-keeping and attention to detail. | 5/18/2022 |
| 6767 | Biomérieux / BioFireBiomérieux / BioFireBiomérieux / BioFire Salt Lake City, UT Lab Technologist I - Oligo, Night Shift BS in Chemistry, Biochemistry, Biology, or related Exp: 0+ years |
Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments. | 5/18/2022 |
| 6768 | Biomérieux / BioFireBiomérieux / BioFireBiomérieux / BioFire Salt Lake City, UT Software Bio-Mathematician I/II - R&D Support BS in Statistics, Mathematics, Bioinformatics, Physics, Computer Science, Engineering, or Computational Biology Exp: 0+ years |
The candidate will be responsible for performing complex mathematical and/or statistical analysis and modeling for projects to support BioFire Diagnostics’ system development and operations groups. The candidate must have strong analytic and programming skills. The candidate will be embedded in the software department but will have close collaboration with multiple departments at BioFire Diagnostics. Therefore, the candidate must have strong communication skills and desire to work in a highly collaborative environment. | 5/18/2022 |
| 6769 | Biomérieux / BioFire Salt Lake City, UT Research Associate BS in Chemistry, Biology, or related Exp: 0-1 years |
You will work with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The RA-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 5/18/2022 |
| 6770 | Biogen Cambridge, MA Associate Scientist II, Research Technology BS in Pharmacology, Neuroscience, Physiology, or other Biological Science Exp: 1-2 years |
As the Associate Scientist II, you will demonstrate expertise in tissue and cell-based in-vitro and ex-vivo assays, preferably including radioligand binding assays (e.g., tissue homogenate binding assays, tissue section autoradiography) used to characterize and develop radiotracers. | 5/20/2022 |
| 6771 | Biogen Research Triangle Park, NC Associate I, Quality Control/Sample Control BS in science or engineering Exp: 1+ years |
Execute the routine processing of samples required for testing by Quality Control Laboratories. Support sample handling activities related to preparation of test samples, use of LIMS applications and communication with various departments in response to requests or inquiries for samples and data. The Associate I is responsible for supporting key functional, tactical, and operational aspects of the QC Sample Control group at Biogen. | 5/20/2022 |
| 6772 | Biogen Research Triangle Park, NC Manufacturing Associate III – Cell Culture / Upstream BS in science or engineering (preferably biology) Exp: 6 months - 2 years |
In cell culture, we work in biosafety cabinets with mammalian cell culture and harvest in shake flasks and wave bags, stainless steel bioreactors, and centrifuges. Our Cell Culture team is looking for a self-starter who takes accountability, is willing to learn quickly in a dynamic environment, and prioritizes accurate and ethical data recordkeeping. Preferred technical skills include prior cell culture, GMP experience, Bioworks or biomanufacturing training, and degrees in microbiology, fermentation engineering, biotechnology, or biology. | 5/20/2022 |
| 6773 | Biogen Research Triangle Park, NC Manufacturing Associate III – Purification / Downstream BS in science or engineering Exp: 6 months - 2 years |
In Purification, we perform critical downstream processing activities within Current Good Manufacturing Practice (cGMP) cleanroom suites at our Research Triangle Park (RTP) facility. These processes include Buffer Preparation, Column Chromatography, Viral Filtration, Ultra Filtration and Bulk Dispensing of the drug substance. Our Manufacturing Associates must be flexible and demonstrate learning agility to perform a variety of complex tasks to produce both clinical and commercial products in a fast-paced environment. | 5/20/2022 |
| 6774 | Biogen Research Triangle Park, NC Manufacturing Associate II (Drug Substance) BS in science or engineering Exp: 0 years |
Execute manufacturing processing steps and/or manufacturing support activities, monitoring the process against the batch record and control system. Document/Record and review cGMP data and information (including documentation of deviations) for processing steps and/or equipment activities, following standard operating procedures. | 5/20/2022 |
| 6775 | Biogen Research Triangle Park, NC EHS Associate II BS in Life Sciences Exp: 1-3 years |
This position will provide support to ensure that site EHS programs comply with Biogen’s EHS management system and external regulatory requirements (i.e., OSHA, EPA, etc.). You will also support IT tools used by EHS for implementation of the site’s EHS training programs, event reporting, document management, and continued maintenance of the site EHS Management System. | 5/20/2022 |
| 6776 | BioGX Birmingham, AL Research Associate BS in Molecular Biology, Chemistry, Biochemistry, or related Exp: 1+ years |
The position executes a range of molecular biology procedures, reagent preparation, bioanalytical procedures, and laboratory duties under supervision. Performs laboratory duties while maintaining associated health and safety guidelines, and is also responsible for maintaining inventory of laboratory reagents and supplies | 5/20/2022 |
| 6777 | BioGX Birmingham, AL Quality Assurance Associate BS or MS in Chemistry, Molecular Biology, or related Exp: 1-3 years |
Provide Quality Assurance (QA) functions in accordance with international standards, regulatory requirements, customer requirements, and BioGX’s quality management system requirements. Review quality control evaluation reports to make determination whether manufactured/processed products meet defined acceptance specifications prior to release. Provide support for the review and oversight of stability studies for manufactured products. | 5/20/2022 |
| 6778 | BioLegend / PerkinElmer San Diego, CA Bioassay Team- Quality Control Associate BS or MS in science or related Exp: 1-2 years |
The candidate will test products by performing binding, enzymatic, proliferation or functional assays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, performing stimulations, maintaining laboratory equipment and supplies. | 5/20/2022 |
| 6779 | BioLegend / PerkinElmer San Diego, CA Biochemist I - Conjugation BS in Biochemistry, Organic Chemistry, or related Exp: 1-5 years |
The candidate will work to support PD flow team for new dye conjugate and other new format developing. The responsibilities will also involve development new products related to immunology research reagents and will support the antibody manufacturing team by troubleshooting and optimizing processes for continuous improvement. The candidate will also explore new technologies and develop new Standard Operating Procedures (SOPs) under the guidance of the Research Scientists. | 5/20/2022 |
| 6780 | BioLegend / PerkinElmer San Diego, CA Cell Biologist - Tissue Culture (Small Scale) BS in Biology, Biochemistry, or related Exp: 1-2 years |
This position offers experience in several areas of tissue culture, in scales ranging from 96 well plates to Roller Bottles. You will also have to opportunity to cross train on a variety of supporting tasks, such as sub-cloning, downstream processing, ELISA assays, mycoplasma detection, and BNII analysis. The primary functions of this position include culturing, setting up, feeding, maintaining, and harvesting of hybridoma cells in roller bottles. (2nd shift M-F 2:30PM to 11:00PM) | 5/20/2022 |
| 6781 | BioLegend / PerkinElmer San Diego, CA Research Associate - Product Development (Antibody Conjugation) BS in Biology, Biochemistry, Chemistry, or related Exp: 6+ months |
This position is lab based and will work independently in a team setting to perform all essential functions related to small scale antibody production, conjugation, and purification. It requires the ability to follow SOPs, complete batch records, and finish assignments in a timely manner. This position will also perform trouble-shooting, and also responsible for assisting the supervisor with laboratory operations and completing production requirements before due dates. | 5/20/2022 |
| 6782 | BioLegend / PerkinElmer San Diego, CA Research Associate - Recombinant Protein & Molecular Cloning BS in Biological Sciences Exp: 0+ years |
This position is responsible for developing cutting edge recombinant protein research products in Molecular Cellular Biology group. The research associate will be involved on developing a new line of recombinant protein products by supporting other team members. The duties include preparing buffer solutions and cell culture media, performing PCR and DNA purification according to standard operating procedures, performing bacterial and mammalian cells cultures, and purifying recombinant proteins with affinity tag. | 5/20/2022 |
| 6783 | BioLegend / PerkinElmer San Diego, CA R&D Materials Coordinator BS in Biology or related Exp: 0-2 years |
The Material Coordinator is an on-site entry level role that is great if you are looking to get away from laboratory work or wanted to learn more about business! In this role, you will support corporate business development efforts to expand company product portfolio through in-licensing, in-house development, and other methods of acquisition. This position will be responsible for documenting, receiving, and distributing incoming materials to stakeholders within the facility and outside locations and will work in a collaborative environment with other internal departments. | 5/20/2022 |
| 6784 | BioLegend / PerkinElmer San Diego, CA Cell Biologist I - Tissue Culture (Large Scale) BS in Biology, Biochemistry, or related Exp: 6+ months |
This position will also allow you to gain experience in all areas of tissue culture and cross training on a variety of other supporting tasks such as downstream processing, ELISA assays, qPCR, mycoplasma detection, and NOVA BioProfile 400 use and maintenance. The primary functions of this position include culturing, setting up, feeding, maintaining, and harvesting of bioreactors with hybridoma cells, finding, testing, and developing new procedures to increase the quality and efficiency of our product and processes. | 5/20/2022 |
| 6785 | Bio-Rad Woodinville, WA Quality Control Specialist I BA or BS in Physical Sciences Exp: 0-2 years |
The QC Specialist position involves production of commercial products with an emphasis on supporting raw material and in-process commercial testing. Specific duties include performing BioPlex QC assays and performing special projects. Testing will include BioPlex testing for assay component raw materials, bulks, fills, raw materials and finished kits tested according to FDA/ISO regulated manufacturing and per document methods employing Good Laboratory Practices. | 5/20/2022 |
| 6786 | Bio-Rad Richmond, CA Quality Control Chemist I BA or BS in Life Sciences Exp: 1-4 years |
Responsibilities: Perform Routine Quality Control Assays in accordance of approved Procedures; Compile data, analyze and summarize results; Troubleshoot assays, as required; Complete instrument and lab maintenance per schedule; Perform inventory of testing materials and order as needed; etc. | 5/20/2022 |
| 6787 | Bio-Rad Woodinville, WA Manufacturing Engineer I BS in science or engineering Exp: 0-2 years |
The Manufacturing Engineer I will perform various troubleshooting tasks, including investigating label printing errors and barcode software troubleshooting, equipment validations, and minor instrument maintenance. Their work will support investigations into deviations and nonconformances that occur in the manufacturing process. Additionally, this ME will investigate root cause of equipment failures and recommend process improvements. | 5/20/2022 |
| 6788 | Bio-Rad Hercules, CA QC Specialist I - Temp BA or BS in Chemistry, Biology, or related Exp: 0-2 years |
The position involves routine testing and logistical activities in the PCR Quality Control group. The incumbent will execute core laboratory testing involving qPCR, Real-Time PCR, droplet digital PCR, SDS-PAGE, and other lab techniques. This position is eligible for a $2,500 hiring bonus. | 5/20/2022 |
| 6789 | Bio-Rad Hercules, CA Research Associate I BS in Chemistry, Biotechnology, Material Science, Polymer Science, Chemical Engineering or related Exp: 0 years |
The successful candidate will perform experiments with supervision in the areas of protein purification as well as some polymer synthesis. This person will design and run experiments, analyze data, interpret results, draw conclusions, and communicate findings to colleagues. The successful candidate will be expected to generate, record, organize, analyze, and present data in an efficient and clear manner. | 5/20/2022 |
| 6790 | BioReference Elmwood Park, NJ Medical Lab Technologist BS in Medical Technology, Chemistry, Biology, or related Exp: 1+ years |
We are looking for a Medical Lab Technician or Technologist for our Cytogenetics Department (40 hours per week) in our Elmwood Park, NJ location. The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 5/20/2022 |
| 6791 | BioReference Elmwood Park, NJ Medical Lab Technologist (FISH) BS in Medical Technology, Chemistry, Biology, or related Exp: 1+ years |
We are looking for a Medical Lab Technician or Technologist for our FISH Department (40 hours per week) in our Elmwood Park, NJ location. The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Must have UroVysion testing experience | 5/20/2022 |
| 6792 | LGC Group Toronto, ON Maintenance and Facilities Associate College Degree (any) Exp: 1-2 years |
You will perform basic facilities and lab equipment preventatives maintenance, trouble shooting, and repair services at the North York and Richmond Hill sites. Troubleshoot facility & production equipment in order to determine if problem must be escalated to a contract service provider. Repair malfunctioning Building services equipment, such as Exhaust fan and HVAC units; this include replacing belts, pulleys, etc. Repair malfunctioning Laboratory equipment, such as high and low vacuum pumps, rotovaps biotags, etc. | 5/20/2022 |
| 6793 | LGC Group Novato, CA GMP Manufacturing Technician I BA or BS in science or engineering Exp: 0+ years |
The GMP Manufacturing Technician I position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the GMP Manufacturing. Maintain batch records, equipment logs and other production records as directed per company. Perform routine operation, maintenance, inspection and cleaning of equipment in accordance with operational instructions. | 5/20/2022 |
| 6794 | LGC Group Petaluma, CA Manufacturing Chemist I BA or BS in Chemistry Exp: 0 years |
The primary responsibility for this position is the synthesis of the fundamental dye and dye free products offered by the company. This requires the utilization of all available resources within the company such as past lot data, R&D and management advice, inferences based upon past experience or current data, large scale equipment, use of computer software programs, and a strong understanding of general and organic chemistry principles. | 5/20/2022 |
| 6795 | LGC Group Petaluma, CA CPG Manufacturing Technician BA or BS in Chemistry Exp: 0-2 years |
As a Solid Support Manufacturing Technician, you will be critical in the operation of the Chemical Production and Manufacturing processes of CPG (Controlled Pore Glass) including at large scale that is absolutely essential to our customers, impacting our mission of Science for a Safer World. You will pivotal in supporting the integration of our scale up and technical transfer projects from Process Development and Research & Development. | 5/20/2022 |
| 6796 | LGC Group Toronto, ON Analytical Chemist BS or MS in synthetic organic chemistry, bioorganic chemistry or related Exp: 0+ years |
As an Analytical Chemist, you will be responsible for analyzing samples from various sources according to our established procedures. Conduct experiments to achieve satisfactory characterization of products while also ensuring effective usage of resources. Interpret and report analysis results in accordance with applicable procedures while adhering to strict guidelines of documentation and reporting. | 5/21/2022 |
| 6797 | LGC Group Gaithersburg, MD Quality Control Analyst BS in science Exp: 1-3 years |
To ensure departmental adherence to Standard Operating Procedures, regulations, and customer requirements. Perform ELISA, Protein and Nucleic Acid Blotting, and related immunoassays, as well as simple wet chemistry, molecular and clinical analyses of both infectious and non-infectious raw material samples and finished products. Support Manufacturing and the Quality Management System through product testing and release, environmental monitoring, internal audits, and facility calibration programs. | 5/21/2022 |
| 6798 | LGC Group Charleston, SC Production Chemist I BS in Chemistry or related Exp: 0-2 years |
The production chemist is responsible for the manufacturing of reference standard solutions by following routine procedures and operations of laboratory equipment. Able to produce and package organic standards quickly and accurately. Operates basic laboratory equipment including analytical balances, syringes, and pipettes. Assists with inventory management of laboratory supplies, chemicals and solutions. | 5/21/2022 |
| 6799 | Bio-Techne Devens, MA Manufacturing Engineer I BS in engineering or related Exp: 0+ years |
The Manufacturing Engineer assists in the plan, design, and maintenance of manufacturing processes. Ensure systems are running according to specifications and within regulations in the production of quality product. Determine parts and tools required for Manufacturing to achieve their goals of producing quality products. The need to meet GMP and ISO standards when developing these procedures is a must. | 5/21/2022 |
| 6800 | Bio-Techne Newark, CA Research Associate BS in biology, chemistry, life science, or related Exp: 0-2 years |
Responsibilities: Execute ISH/IHC-based assays to support new product development and assay optimization; Participate in the experimental design with Scientific Leader(s), assay running, data collection and interpretation; Participate in the compilation and presentation of data to the project team or other departments; Support manufacturing QC for commercial product testing, release and troubleshooting when needed | 5/21/2022 |
| 6801 | Bio-Techne Minneapolis, MN Advanced Research Associate, Protein Development (Cell Culture) BS in microbiology, biology, biochemistry, bioprocess engineering, chemistry, or related Exp: 0-2 years |
A Research Associate is responsible for development of cell culture protocols for new recombinant protein products. This includes screening clones and testing growth conditions and media formulations in bioreactors and other culture formats, in small to medium scale. It may also include cooperation with the molecular biology group in creation of new clones, creation and characterization of new cell lines, and screening studies in search for novel protein product targets. | 5/21/2022 |
| 6802 | Ensoma Boston, MA Research Associate/Sr. Research Associate, Bioanalytical Assay Development MS degree Exp: 0 -3 years |
Ensoma seeks a highly motivated Research Associate / Associate Scientist to join its Bioanalytical team. This is an ideal position for an individual with a background in biology, molecular biology, biochemistry or a related field who thrives in a team-oriented, fast-paced, and cross disciplinary biotech environment. The candidate will be an integral member of a small team of scientists across therapeutic discovery and translational sciences aiming to rapidly and pragmatically realize the potential of an emerging technology by supporting target engagement, PK/PD and tolerability studies in preclinical settings. | 5/16/2022 |
| 6803 | Erbi Biosystems Stoneham, MA Research Associate Bachelor’s degree in a life science Exp: 0 to 2 years |
The Research Associate is responsible for executing a wide variety of laboratory tasks and/or experiments in a high-quality research environment following Standard Operating Procedures (SOPs). Good judgment and problem-solving skills are required for recognizing process deviations, participating in troubleshooting, and operation of complex laboratory instrumentation. The Research Associate is expected to organize their work and data collection according to company standard formats. A successful candidate possesses excellent attention to detail and the eagerness to work in a Team Science, data-driven atmosphere. | 5/16/2022 |
| 6804 | Etubics Culver City, CA Research Associate Bachelors degree Exp: 1 - 2 years |
ImmunityBio Inc. is seeking a highly motivated, full-time research associate to join the Protein Science group to support the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate should have a bachelor’s degree with 1-2 years of wet-lab experiences, ability to manage multiple tasks in a timely manner, good written/verbal communication skills and have a willingness to work as part of the team. ImmunityBio Inc. is seeking a highly motivated, full-time research associate to join the Protein Science group to support the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate should have a bachelor’s degree with 1-2 years of wet-lab experiences, ability to manage multiple tasks in a timely manner, good written/verbal communication skills and have a willingness to work as part of the team. | 5/16/2022 |
| 6805 | Etubics Culver City, CA Research Associate, Cell Line Development Bachelor's degree in Biochemistry, Biology, Chemistry, Life Science or other related discipline Exp: 1 - 3 years |
ImmunityBio seeks a highly motivated, full-time research associate to work in our cell line development group. The group's responsibility is to take novel cancer therapeutics (mAbs/fusion proteins) from the R&D group and create a stable therapeutic production process to handoff to PD and manufacturing. The ideal candidate should possess a bachelor's degree in science or engineering, exceptional verbal and written communication skills, good work habits, and willingness to work as part of a team. Experience working in a wet lab environment outside of a classroom is strongly preferred. | 5/16/2022 |
| 6806 | Fabric Genomics Oakland, CA Clinical Genomic Scientist M.Sc in human genetics, cancer biology, molecular biology, or related field M.Sc in human genetics, cancer biology, molecular biology, or related fi Exp: 1-3 years |
We are looking for an experienced Clinical Genomics Scientist to work on analysis of clinical NGS-based tests from our laboratory customers. This is a unique opportunity to work closely with a strong team of geneticists, genetic counselors, bioinformaticians, and other professionals who are shaping the future of personalized medicine. As a clinical genomic scientist you will actively participate in variant interpretation, cases analysis and clinical reporting for some of the leading genomics companies in the world, which provide a path for families and individuals to end their medical odyssey and get appropriate access to exome, genome or NGS panel tests and counseling services. You will also engage with the product development and software engineering groups to create innovative software and workflows that facilitate clinical interpretation and classification of genetic information with our product. We are looking for an experienced Clinical Genomics Scientist to work on analysis of clinical NGS-based tests from our laboratory customers. This is a unique opportunity to work closely with a strong team of geneticists, genetic counselors, bioinformaticians, and other professionals who are shaping the future of personalized medicine. As a clinical genomic scientist you will actively participate in variant interpretation, cases analysis and clinical reporting for some of the leading genomics companies in the world, which provide a path for families and individuals to end their medical odyssey and get appropriate access to exome, genome or NGS panel tests and counseling services. You will also engage with the product development and software engineering groups to create innovative software and workflows that facilitate clinical interpretation and classification of genetic information with our product. | 5/17/2022 |
| 6807 | Flexion Therapeutics San Diego, CA Research Associate I Bachelor’s degree in relevant field of study (e.g. chemistry, pharmacy, biology, engineering, etc.) from an accredited college or university. Exp: 1 year |
The purpose of this position is to carry out assigned laboratory duties which may include sampling, testing, and evaluating analytical data on samples such as raw materials, in-process, and final products. | 5/17/2022 |
| 6808 | Flexion Therapeutics San Diego, CA QC Analyst 1 BS degree in Chemistry from an accredited college or university Exp: 1 year |
The purpose of this position is to carry out assigned laboratory duties which may include sampling, testing, and evaluating analytical data on samples such as raw materials, in-process and final products. | 5/17/2022 |
| 6809 | Fluxergy Irvine, CA Research Assistant - Microfluidics B.S. with degrees in Life Science or Engineering disciplines or related fields Exp: 0-2 years |
As a Research Assistant in the Microfluidics department, you will be part of an expanding System Integration team, and will apply your knowledge and skills in the fields of microfluidics, materials, surface engineering, biochemistry to help develop the next generation of Fluxergy Test Card, a microfluidic consumable aiming at transforming point-of-care diagnostic systems. You will be expected to conduct, analyze, and report on experiments to develop new Test Card from feasibility through validation for the Fluxergy platform. As Research Associate, you will work closely with a cross discipline team of R&D and Production Engineers and Technicians to develop new products. This position requires a highly motivated, independent worker who has a strong desire to bring products to the mark | 5/17/2022 |
| 6810 | Frontida Biopharm Vandalia, OH Microbiologist Bachelor degree in Biology/Microbiology or related field Exp: 0 to 2 years |
The essential job function is to participate in entry level microbial testing of incoming raw materials and perform sampling and testing of the facility USP Water system. | 5/17/2022 |
| 6811 | Frontida Biopharm Vandalia, OH Quality Control Analyst I A Bachelor degree in Chemistry or related field Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. This position works 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday etc.The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. This position works 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday etc. | 5/17/2022 |
| 6812 | Frontier Medicines South San Francisco, CA Research Associate, In vivo Pharmacology BS in biological science (animal science, pharmacology, cellular biology, or related discipline) Exp: 1+ years |
Frontier medicines is seeking a highly motivated individual to fill the position of Research Associate in the Disease Biology teams In Vivo group. The successful candidate is expected to have a working knowledge of in vivo research and mouse models of oncology. This position requires working as part of a multidisciplinary team in a fast-paced drug-hunting environment. This position is located in South San Francisco. | 5/18/2022 |
| 6813 | Frontier Medicines Boston, MA Research Associate, Disease Biology - Boston BSc or MSc in a biological science (biochemistry, molecular biology, cellular biology or related discipline). Exp: 1-3 years |
Frontier Medicines is seeking a highly motivated individual to fill the position of Research Associate in the Disease Biology team. The successful candidate is expected to have an excellent working knowledge of molecular and cell biology techniques in oncology research. This position requires working as part of a multidisciplinary team in a fast-paced drug-hunting environment. | 5/18/2022 |
| 6814 | FUJIFILM Diosynth College Station, TX Manufacturing Tech III (Night Shift) Bachelor’s degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering or other related field Exp: 1 years |
The Manufacturing Technician III will work directly with a range of technologies. Dependent upon assignment, the range of technologies. | 5/18/2022 |
| 6815 | GenMark Diagnostics [Roche] Seattle, WA Research Associate Bachelor’s degree in Biological/Life Sciences, Chemistry, Organic Chemistry, Chemical Engineering, Biochemistry or related field Exp: 0-2 years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its unique chemistry that advances DNA sequencing by nanopore, Sequencing by eXpansion (SBX™). You will engineer and synthesize the molecular building blocks for our novel technology. These building blocks translate DNA sequences into a simple to measure surrogate, the Xpandomer, which significantly improves the accuracy and throughput of nanopore sequencing. The Molecular Engineering group is passionate about the novel molecules they have developed and the impact SBX technology can have on advancing sequencing and patient outcomes. We are looking for people who are excited about the significance of our technology and want to make SBX successful. Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its unique chemistry that advances DNA sequencing by nanopore, Sequencing by eXpansion (SBX™). You will engineer and synthesize the molecular building blocks for our novel technology. These building blocks translate DNA sequences into a simple to measure surrogate, the Xpandomer, which significantly improves the accuracy and throughput of nanopore sequencing. The Molecular Engineering group is passionate about the novel molecules they have developed and the impact SBX technology can have on advancing sequencing and patient outcomes. We are looking for people who are excited about the significance of our technology and want to make SBX successful. | 5/18/2022 |
| 6816 | GenMark Diagnostics [Roche] Carlsbad, CA Research Associate I B.S. degree in Bioengineering, Biochemistry, Molecular biology or related field Exp: zero (0) to two (2) years |
The position requires the execution of a range of data analysis and laboratory duties under minimal supervision. Position may include some molecular biology procedures, reagent preparation. This individual will work closely with cross functional teams to investigate root cause of anomalies reported during Quality Control or improve processes in the manufacturing process. | 5/18/2022 |
| 6817 | GenMark Diagnostics [Roche] Carlsbad, CA Quality Assurance Specialist A Bachelor of Science in related industry Exp: 1-3 years |
This position is responsible for GMP compliance and supports in supplier quality processes. Represents Quality Assurance and interacts with cross-functional departments to provide quality guidance. Ensure compliance with all relevant quality management system and regulatory requirements (e.g., ISO 13485, 21 CFR 820). Stakeholder in the development, implementation, and continued improvement of quality systems within the QA department. The work arrangement for this position is hybrid (remote and on-site, as needed). | 5/18/2022 |
| 6818 | GenMark Diagnostics [Roche] Branchburg, NJ Quality Operations Technician (M-F 3:00pm - 11:30pm) Bachelor's Degree Preferred Exp: Less than one year |
This position is for the 2nd shift, typical hours are M-F 3:00pm to 11:30pm. | 5/18/2022 |
| 6819 | GenMark Diagnostics [Roche] Carlsbad, CA Research Associate II MS degree in Bioengineering, Biochemistry, Molecular biology or related field Exp: zero (0) to two years |
We are seeking an enthusiastic individual to join our Product Technical Support team. The position requires the execution of a range of molecular biology procedures, reagent preparation, data analysis, and laboratory duties under supervision. This individual will work closely with cross functional teams to investigate the root cause of anomalies reported during Quality Control or from the manufacturing floor. | 5/18/2022 |
| 6820 | Glympse Bio Cambridge, MA Research Associate/Sr. Research Associate, Chemistry high throughput screening BS or MS equivalent degree in chemistry, biochemistry, biology or relevant discipline Exp: 1-3 years |
Our Screening and Automation group is seeking a motivated Research Associate who will contribute to the development of novel diagnostics in our Chemistry platform. This person will perform work at the intersection of Chemistry, Biology and Computational Science, participating in experimental design and execution, generating data, and collaborating on analyses. The individual we hire will have the opportunity to lead screening campaigns, execute on established workflows, optimize and develop new assays, and help build out new tools and functionalities. | 5/18/2022 |
| 6821 | GRAIL Menlo Park, CA Research Associate I/II - R&D - #2157 B.A./B.S. degree in biology, biochemistry, microbiology, molecular biology, or equivalent Exp: 1-2 years |
As a Research Associate in GRAIL’s R&D Group, you will play an integral role in the development of new technologies and applications for genomics-based clinical assays. The ideal candidate should be detail-oriented and have experience with blood processing, nucleic acid extraction, next-generation sequencing (NGS), and strong molecular biology skills. Experience working with RNA is a plus. Troubleshooting skills are a must. | 5/18/2022 |
| 6822 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to help confirm mailing addresses in our directory. Mostly Googling. Can do work any time, any place. Must be able to accept payment via PayPal. If interested, send a message through the contact form. Thanks! | 05/18/22 |
| 6823 | Avantor Carpinteria, CA Controls Engineer BS in Electrical or Mechanical Engineering, or Computer Science Exp: 1-3 years |
The Controls Engineer, under increasingly limited supervision, will work closely with R&D, Manufacturing, Reliability & Maintenance Engineering, and Process Engineering to design, build, install, and support control system equipment and upgrades to support NuSil's needs. Design electrical schematics, physical electrical enclosure layouts, conduit runs, and PLC/HMI code for new or upgraded equipment, following applicable NFPA, NEC, and other standards. | 5/8/2022 |
| 6824 | Avantor Bakersfield, CA QC Technician - Testing BS in science Exp: 1-2 years |
Under close supervision, responsible for technical quality tasks, including inspecting and processing raw materials and reviewing and releasing finished products. Perform Batch Record Review and manufactured product release processing. Observe cGMP good documentation practices. | 5/8/2022 |
| 6825 | Avantor Bridgewater, NJ Associate Scientist - Process Development BS in science Exp: 6+ months |
Responsibilities include: Supporting pilot plant production & maintenance activities; Preparing buffers, experiments, and samples for analyses; Writing batch paperwork; ordering and handling of raw materials, lab supplies, and equipment; preparing materials in the pilot plant; monitoring pilot and scale-up manufacturing; conducting processing studies; Obtaining and evaluating product samples as needed | 5/8/2022 |
| 6826 | Avantor Bridgewater, NJ Associate Scientist - Downstream MS in biochemistry, molecular biology, chemistry, cell biology, chemical engineering, or bioengineering Exp: 6+ months |
Responsibilities include: Executing and supporting downstream purification (e.g., monoclonal antibodies, fusion proteins, etc.) on a bench-scale jointly with other scientists or independently; Conducting pilot-scale material generations with the team; Preparing and executing experimental protocols and analytical test methods under general guidance; Accurately documenting all procedures and observations | 5/8/2022 |
| 6827 | Avantor Paris, KY Quality Control Lab Analyst BS in Chemistry, Biology, Microbiology, or related Exp: 1-3 years |
Under limited supervision, responsible for completing product quality checks. Conduct non-routine and complex testing and analysis of production work. Quality checks are typically not reviewed for accuracy. Documents quality control issues as needed. Maintain work activities to meet operational requirements. Monitor staff performance in accordance to established standards. | 5/8/2022 |
| 6828 | Avantor Bakersfield, CA QC Technician (3rd Shift) BS or BA in Chemistry or related Exp: 1-2 years |
Under close supervision, responsible for technical quality tasks, including inspecting and processing raw materials and reviewing and releasing finished products. Perform Batch Record Review and manufactured product release processing. Observe cGMP good documentation practices. | 5/8/2022 |
| 6829 | Avecia Milford, MA Quality Control Analyst BS in Chemistry, Biology, or related Exp: 1-8 years |
The position is responsible for performing routine and non-routine analyses of raw materials, in-process materials and finished products. The position may provide training and guidance to other QC Analysts. Position troubleshoots problems associated with methods and instruments resolving them where possible or seeking guidance/authorization where required. | 5/8/2022 |
| 6830 | Avecia Milford, MA Manufacturing Chemist (All Shifts and Levels) BS or BA in Chemistry or related Exp: 0+ years |
Responsibilities: Execute defined lab start up and shutdown procedures; Maintaining a clean and organized work environment in accordance with defined procedures; Assuring basic lab supply needs are met; Qualify and maintain Qualification on all assigned manufacturing processes | 5/8/2022 |
| 6831 | Avecia Milford, MA Research Scientist I MS in science or engineering Exp: 1+ years |
This position is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. Analyze test samples, process data, and report results with minimal errors. | 5/8/2022 |
| 6832 | Avecia Cincinnati, OH Quality Control Analyst I BS or BA in Chemistry or related Exp: 0+ years |
The QC Analyst I is responsible for executing quality control analytical tasks for one or more projects to support testing and release of oligonucleotides. Sample, test and release raw materials and finished products per established procedures. Follow written protocols to package and label stability studies. Perform routine analyses using techniques such as: Wet Chemistry, Karl Fischer, UV-Vis, FT-IR, Raman, LC, and GC | 5/8/2022 |
| 6833 | Avecia Cincinnati, OH Quality Assurance Associate BS or BA in science Exp: 1-3 years |
Responsibilities: Writes SOP’s, protocols, validation plans and compliance documents for cGMP program; Acts as departmental resource for cGMP programs; Oversees qualification of instruments, equipment, facility, clean rooms and computer hardware - software; Sets-up and organizes tracking program for equipment used in cGMP work; Reviews and authorizes batch production records and quality control documentation | 5/8/2022 |
| 6834 | Averica Discovery Milford, MA Scientist - Entry Level BS in Chemistry or related Exp: 0 years |
You will participate in all aspects of the Company’s laboratory programs, including client projects and independent research using analytical instrumentation, technologies, and procedures. Key techniques will include chromatography, both HPLC and Supercritical Fluid Chromatography (SFC), and NMR and mass spectrometry. | 5/8/2022 |
| 6835 | Aviva Systems Biology San Diego, CA Manufacturing Associate I/II BS or MS in Life Sciences Exp: 1+ years |
The Manufacturing Associate works as part of a multidisciplinary team performing standard molecular biology techniques, protein purification and analysis, and cell culture maintenance. Prepare buffers following GMP procedures. Perform preventative maintenance on manufacturing equipment. Grow microbes such as E. coli and S. cerevisiae for use in large-scale protein purification. | 5/8/2022 |
| 6836 | Aviva Systems Biology San Diego, CA Research Associate I/II - Protein Biochemistry BS or MS in Life Sciences Exp: 1+ years |
The Research Associate will assist in the development of recombinant proteins and technologies, as well as antibody-based workflow solutions including Western Blot, ELISA, and IF applications. Perform routine biochemistry and molecular biology techniques such as cloning, RNA/DNA isolation, and protein purification. Perform small-scale bacterial, fungal, and mammalian cell culture using aseptic techniques. Operate incubator/shakers, centrifuges, and other laboratory equipment used in protein production. | 5/8/2022 |
| 6837 | Element Bend, OR Chemist I BS in Chemistry or related Exp: 0 years |
Your primary responsibility is to support laboratory operations by conducting analytical chemistry testing. Perform basic measurements such as pH/conductivity, UV-Vis and TOC. Perform project tasks under direction of a project lead (e.g. extraction, sampling, sample analysis). Depending on experience and need, assist with advanced analytical instrumentation (e.g., GC-MS, LC- MS, ICP-MS). | 5/8/2022 |
| 6838 | Element Ann Arbor, MI Instrumentation Specialist - Pharmaceuticals BS in science or related Exp: 1+ years |
This position is responsible for developing and executing installation, operational, and performance qualification protocols on instruments and equipment that is compliant with regulatory requirements. | 5/8/2022 |
| 6839 | Element Ann Arbor, MI Chemist BS or MS in Chemistry, Materials Science, Polymer Science, or related Exp: 1-3 years |
The Chemist will test, develop and improve formulations in consumer products opportunity space, perform testing using a variety of technologies and draw conclusions based upon analytical data. Work is performed under the supervision of the lab manager. | 5/8/2022 |
| 6840 | Element Acton, MA Microbiologist BS in Microbiology Exp: 1-2 years |
Provide essential microbiological analytical laboratory services for food and beverage manufacturers, private sectors, commodity exporters companies and food industry in line with Element's standards. Maintain accurate records of all performed procedures in assisting in implementation of ISO/IEC 17025:2005 in the laboratory. | 5/8/2022 |
| 6841 | Axogen Burleson, TX Quality Inspector BS in Life Sciences Exp: 6 months - 1 year |
The Quality Inspector will be responsible for inspecting materials and products for conformance to specifications using specified measuring instruments and methods. Ensures materials and products are in accordance with established tolerance levels for quality and performance and are not irregular or damaged. Responsible for ensuring all policies and procedures are in compliance with applicable with FDA, state OSHA and ISO regs and standards. | 5/8/2022 |
| 6842 | Axsome New York City, NY Clinical Trial Assistant BS in Life Sciences or Nursing Exp: 1+ years |
The Clinical Trial Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. Responsibilities: Create and maintain study trackers (e.g., contact lists, study status trackers, enrollment); Ensure accurate and up to date information in clinical trial management system (CTMS); Review and maintain documents in the Trial Master File (TMF) | 5/8/2022 |
| 6843 | Aziyo Biologics Calverton, MD R&D Associate MS in Biology, Bioengineering, or related Exp: 1-3 years |
This position will work in a collaborative team environment to design assays for the scientific characterization and development of tissue-based and biomaterial products in compliance with Aziyo’s quality and regulatory standards. The successful candidate will execute, optimize, and analyze a broad range of bioassays, biomechanical and material characterizations, and product prototyping. In addition, this position will support the development of manufacturing processes, including scale up for full production and/or production transfer. | 5/9/2022 |
| 6844 | Inotiv Gaithersburg, MD Pathology Technician I BS or BA in Biology, Life Sciences, Chemistry, or related Exp: 0 years |
Responsibilities: Learns how to review study protocol and ensure study tasks and data for pre-clinical research studies are conducted in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. Learns to serve as head technician for general toxicology and DART studies and to perform protocol review in preparation for PI meeting attendance. Position requires the ability to manage multiple studies within scope of expertise. | 5/9/2022 |
| 6845 | Inotiv Gaithersburg, MD Associate Scientist I BS in Biology, Chemistry, Biochemistry, or related Exp: 1+ years |
Perform a wide variety of in vitro assays or tests required to characterize product or material safety. Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations. Maintain an understanding of technological principles and applications of the organization’s services. | 5/9/2022 |
| 6846 | Inotiv Raleigh, NC Research Assistant (Genetic Toxicology) - 2nd Shift BS or Associates in Biology or related Exp: 0-3 years |
The Research Assistant will perform laboratory maintenance tasks; maintain supply inventories and prepare purchase orders as needed; maintain/archive study books; handle data; assist in preparation of posters/presentations; initiate preparation and/or modification of protocols, reports, SOPs, assay forms, etc. Other tasks may include performing flow cytometry-based assays, maintaining and dosing cultured cells, and interacting with vendors to learn/troubleshoot procedures as skill level and training dictate. | 5/9/2022 |
| 6847 | Inotiv Gaithersburg, MD Associate Scientist I (Secondary Assays) BS in Biology, Chemistry, Biochemistry, or related Exp: 1+ years |
Responsibilities: Perform a wide variety of in vitro or in vivo Comet assays or tests required to characterize product or material safety; Maintain sterile and good cell/tissue culture techniques; Prepare study reagents in accordance with SOPs and study instructions; Conduct pre-designed assays using basic laboratory techniques and skills | 5/9/2022 |
| 6848 | Inotiv Gaithersburg, MD Associate Scientist I (In Vitro Cytogenetics) BS in Biology, Chemistry, Biochemistry, or related Exp: 1+ years |
Responsibilities: Perform a wide variety of in vitro assays or tests required to characterize product or material safety; Maintain sterile and good cell/tissue culture techniques; Prepare study reagents in accordance with SOPs and study instructions; Conduct pre-designed assays using basic laboratory techniques and skills | 5/9/2022 |
| 6849 | Baxter Bloomington, IN Quality Lab Associate I (Weekend Day) BS in Chemistry, Biology, or related Exp: 0+ years |
The Quality Lab Associate I performs entry-level laboratory testing (pH, density, volume, etc.) that requires a variety of chemical, biological, or physical analyses on products/systems in support of the company’s quality program. This opening is on the weekend day shift: 7:00 AM - 7:00 PM | 5/9/2022 |
| 6850 | Baxter Round Lake, IL Quality Lab Associate I (1st Shift) BS in Chemistry or related Exp: 6+ months |
Conduct critical chemical and physical analyses on Raw Materials, Initial, In-process and Final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities. Work under minimum supervision. Use sophisticated laboratory instrumentation (HPLC, FTIR, UV, GC etc.) and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles. | 5/9/2022 |
| 6851 | Baxter Round Lake, IL Quality Engineer - Renal BS in Biomedical, Electrical, or Mechanical Engineering Exp: 1+ years |
Review individual complaints and associated service data to determine risk level and complete investigation into the “As Determined” problem and cause coding for each complaint. Utilize Excel to compile and create trending information for input into the sustaining products organization. Analyze data from various quality inputs (including but not limited to: nonconformance, FCA, complaints, MDR, etc.) to determine trends and systemic issues. | 5/9/2022 |
| 6852 | Baxter Round Lake, IL Supplier Quality Analyst BS in science or engineering Exp: 1+ years |
The Quality Analyst I is responsible for leading periodic supplier requirement reviews, identifying and resolving gaps, and maintaining supplier qualification files in Baxter’s electronic supplier quality database. You will act as a liaison for the Supplier Quality team to global facilities, businesses, and regions. You will also review and approve manufacturing records (batch and DHR records) for products manufactured by Contract Manufacturing Organizations to ensure accuracy and completeness. | 5/9/2022 |
| 6853 | Baxter Marion, NC Engineer I - Process & Reliability BS in science or engineering Exp: 0-1+ years |
Performs data analysis to identify opportunities to improve maintenance metrics or personnel knowledge and skill sets, ultimately increasing asset availability. Uses data to recommend improvements in the Equipment Maintenance Plans (EMP) based on CMMS, FMEA, RCA, VMB and other streams of asset and systems reliability data. Works to improve asset and system process and reliability with an emphasis on Mean Time Between Failure (MTBF), and the resulting implementation of mitigation or elimination solutions. | 5/9/2022 |
| 6854 | Be Biopharma Cambridge, MA Research Associate, Oncology MS in molecular or cellular biology, immunology, or related Exp: 1+ years |
Responsibilities: Help to establish protocols around differentiation of primary immune cells, including extensive tissue culture work (maintenance, expansion, and banking); Handling and analyzing workflows pertaining to cellular differentiation and profiling with downstream qRT-PCR, protein quantification, and other molecular readouts; Cloning of constructs to support cellular engineering efforts | 5/9/2022 |
| 6855 | Be Biopharma Cambridge, MA Associate Scientist, Cell Engineering MS in Molecular Biology, Bioengineering, Immunology, or related Exp: 1-5 years |
Responsibilities: Help to perform and optimize genome engineering protocols for primary B cells; Support characterization of engineered B cells using targeted amplicon sequencing, ddPCR and NGS-based assays as well as molecular biology techniques including qPCR, Western blotting, ELISA, and others; Contribute to the cloning of DNA constructs and support identification of safe and potent genome engineering reagents; Independently design experiments, acquire data, and analyze results | 5/9/2022 |
| 6856 | Beaufort Virginia Beach, VA Clinical Trial Assistant BS in science Exp: 0+ years |
Responsible for the clinical document processing and filing associated with a clinical study, as well as preparing/maintaining project files (both electronic and hard-copy), documentation binders, clinical forms and logs, and other administrative tasks. Work with other members of a project team to conduct phone screens with hospitals, doctor's offices and other clinical sites that are interested in participating in the studies that Beaufort manages. | 5/9/2022 |
| 6857 | Berg Framingham, MA Research Associate I BS in Chemistry, Biochemistry, or related Exp: 0+ years |
Assist in high-throughput sample preparation of patient clinical samples in a team-oriented environment. Analyze and report the experiment data in an organized and time-efficient manner. Maintain, operate, and troubleshoot chromatography and mass spectrometry instruments. | 5/10/2022 |
| 6858 | Berg Framingham, MA Research Associate II BS or MS in Chemistry, Biochemistry, Neuroscience or related Exp: 1-2 years |
Assist in the characterization of novel diagnostic biomarkers and therapeutic targets for Alzheimer’s and Parkinson’s disease using standard molecular biology techniques. Identification, development, and implementation of cutting-edge methods for characterizing lead biomarker and therapeutic candidates. Maintain and differentiate several cell lines to support the research efforts of the Neurology department. | 5/10/2022 |
| 6859 | Berkeley Lights Emeryville, CA Research Associate, Applications Engineering BS in Biology, Chemical Engineering, Bioengineering, Biomedical Engineering, or related Exp: 0-3 years |
In this new role, you will learn to operate very sophisticated and innovative instruments and support the ongoing development of our platforms. The ideal candidate possesses a strong attention to detail and has demonstrated lab skills experienced in techniques of modern molecular and cell biology or complex biotech instrumentation. You will take ownership for achieving results in biology and technology development programs. | 5/10/2022 |
| 6860 | Berkeley Lights Emeryville, CA Associate Applications Development Engineer BS or MS in Chemical Engineering, Mechanical Engineering, Electrical Engineering, Bioengineering, Biomedical Engineering, Biophysics, or related Exp: 0-3 years |
Responsibilities: End-to-end workflow development involving precious sample handling, microfluidic-based workflow development, and workflow automation; Validation and verification of complex life science instrumentation; Contribution to the invention of core intellectual property (from conception through validation), white papers, and external publications. | 5/10/2022 |
| 6861 | BioAssay Systems Hayward, CA Research Associate - Assay Development BS in biochemistry, chemistry, biology, or related Exp: 1-2 years |
This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers. | 5/10/2022 |
| 6862 | BioAssay Systems Hayward, CA Research Associate - Manufacturing BS in biochemistry, chemistry, biology, or related Exp: 1-2 years |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing, and packaging the finished products. This candidate may also join part time in our R&D team. | 5/10/2022 |
| 6863 | WuXi Apptec Cranbury, NJ Associate Scientist I Bachelor's degree in chemistry or closely related physical science Exp: 0 - 3 years |
The Associate Scientist I is responsible to conduct and/or provide support for various types of in vitro ADME assays in support of discovery and development programs in the DMPK department. | 5/9/2022 |
| 6864 | WuXi Apptec Cranbury, NJ Associate Scientist I Bachelor's degree in biology, chemistry, pharmacology or closely related majors Exp: 0 - 3 years |
The Associate Scientist I is responsible to conduct and/or provide support for various types of Bioanalytical assays in support of discovery programs in the DMPK department. | 5/9/2022 |
| 6865 | Cellarity Cambridge, MA Research Associate, Next Generation Sequencing BS/MS (or equivalent) in molecular biology, biochemistry, biology or related field Exp: 1+ year(s) |
Cellarity, Inc. is seeking a Research Associate with Next Generation Sequencing (NGS) experience to join our Technology group to carry out large-scale data generation. The candidate will work both independently and as part of a collaborative team to generate data from various genomics-oriented workflows and assist in the optimization and validation of new technologies and procedures. The candidate must be detail oriented, have strong communication skills and be willing to work in a dynamic entrepreneurial environment. | 5/10/2022 |
| 6866 | CODEX DNA San Diego, CA Research Associate (Protein Expression) BS degree in Life Sciences, Chemistry, Chemical Engineering, Bioengineering or a related discipline Exp: 1+ years |
An exciting role has just become available at Codex DNA. We are seeking a curious and energetic Research Associate who will take ownership of automating & building out pipelines for protein synthesis, screening, and expression. This person will report to the Team Lead within the R&D group and will have an opportunity to contribute to the development of new products and building our business around our biopolymer-printer. The role will require a good understanding of molecular biology, protein analysis, and experimental design. A successful candidate will enjoy working in a fast-paced and a highly collaborative start-up environment doing cutting-edge science. This person will work closely with personnel from the R&D, Engineering, and Biofoundry Services. | 5/10/2022 |
| 6867 | CTK Biotech Poway, CA Antibody Development Research Assistant/Research Associate B.S. or M.S. in Biochemistry, Cell Biology, Molecular Biology or related field. Exp: 1+ year |
CTK is seeking a highly motivated, team-oriented Research Assistant/Research Associate for development of antibody and other recombinant proteins. Activities will include antibody cloning, cell culture and transfection, protein purification, and characterization. | 05/11/2022 |
| 6868 | CytomX Therapeutics South San Francisco, CA Research Associate I/II Analytical & Formulation Development B.S. in analytical chemistry, biochemistry, pharmaceutical development or related field Exp: 0 to 3 years (for RA I); 1 to 5 years (for RA II) |
Joining a collaborative, productive and dynamic team to provide analytical development support for advancing exciting CytomX clinical programs into late-stage development and commercial launch. Ample opportunities for career development and growth.Joining a collaborative, productive and dynamic team to provide analytical development support for advancing exciting CytomX clinical programs into late-stage development and commercial launch. Ample opportunities for career development and growth. | 5/11/2022 |
| 6869 | CytomX Therapeutics South San Francisco, CA TEMP Research Associate I/II Analytical & Formulation Development B.S. in analytical chemistry, biochemistry, pharmaceutical development or related field Exp: 0 to 3 years (for RA I); 1 to 5 years (for RA II) |
Join a collaborative, productive and dynamic team to provide analytical development support for advancing exciting CytomX clinical programs into late-stage development and commercial launch. This role is a contract position for 4+ months. | 5/11/2022 |
| 6870 | CytomX Therapeutics South San Francisco, CA Research Associate I, Protein Sciences MS in Biochemistry Exp: 1 year |
We seek a highly motivated individual to participate in the purification and characterization of Probodies, various bispecific molecules (TCBs) and Procytokines to support all discovery and development programs at CytomX. The successful candidate will work as a Research Associate I in the Protein Sciences department. We seek a highly motivated individual to participate in the purification and characterization of Probodies, various bispecific molecules (TCBs) and Procytokines to support all discovery and development programs at CytomX. The successful candidate will work as a Research Associate I in the Protein Sciences department. | 5/11/2022 |
| 6871 | Decipher Biosciences San Diego, CA Research Associate I, Assay Development B.Sci. in biological sciences (or related field) Exp: 1-2 years |
The Research Associate I will support the Assay Development team at Decipher Biosciences; assisting in research, development, and optimization of genomic assays, and supporting general laboratory maintenance and document control. Other responsibilities might be applied as needed. | 5/11/2022 |
| 6872 | Deepcell Menlo Park, CA Research Associate/Senior Research Associate, Biology Bachelor’s degree or Master’s degree in bioengineering, molecular biology, cell biology, genetics, or similar field Exp: 1+ years’ |
We are looking for multiple research associates to join the biology team and help us to unlock the power of cell morphology and connect the genome to the patient. | 5/11/2022 |
| 6873 | Denison Pharmaceuticals Lincoln, RI Quality Engineer Bachelor's degree in Science or related field Exp: 1-3 years |
The successful candidate for the position of Quality Engineer shall be fully capable of performing all job functions and qualifications listed. | 5/11/2022 |
| 6874 | DiabetOmics Hillsboro, OR Research Assistant/Associate in Product Development (2 positions available immediately) BA/BS in a relevant biological science Exp: 1-2 years |
Applies knowledge of scientific principles and concepts to the design, development, and execution of Product Development experiments. Demonstrates technical proficiency, scientific creativity, collaboration with others and can work independently. Under guidance of senior personnel, designs and conducts research and/or product development, assay optimization and scale-up tasks and experiments based on the needs of the group. Ensures compliance with and helps to implement the requirements of working in a regulated environment to assure adherence to various requirements, including Design Control, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP). Helps to coordinate general laboratory tasks such as reagent preparation, inventory and organization of work.Applies knowledge of scientific principles and concepts to the design, development, and execution of Product Development experiments. Demonstrates technical proficiency, scientific creativity, collaboration with others and can work independently. Under guidance of senior personnel, designs and conducts research and/or product development, assay optimization and scale-up tasks and experiments based on the needs of the group. Ensures compliance with and helps to implement the requirements of working in a regulated environment to assure adherence to various requirements, including Design Control, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP). Helps to coordinate general laboratory tasks such as reagent preparation, inventory and organization of work. | 5/11/2022 |
| 6875 | Dicerna Pharmaceuticals Boulder, CO Research Associate/ Senior Research Associate -CMC Chemical Development Nucleic Acids Specialist BS Exp: >0 Years |
Dicerna Pharmaceuticals is seeking highly motivated scientists to join its CMC Chemical Development team in Boulder, Colorado. The candidate will be expected to be a key technical resource for the manufacture of raw materials used in the manufacture of Dicerna products, Optimizing the manufacturing process, establishing new manufacturing capacity and supporting oversight of existing manufacturers. The successful candidate will be responsible for synthesis and process development of novel carbohydrates, nucleosides and phosphoramidites. We are currently looking for chemists of varying skill sets for this position and the title will be suited to the experience level of the candidate. This position will support therapeutic programs in multiple disease areas and be a key contributor to securing the supply chain for Dicerna’s GalXC | 5/11/2022 |
| 6876 | Dicerna Pharmaceuticals Lexington, MA Research Associate/Associate Scientist, Discovery Research BS/MS in Biology, Biochemistry, Pharmaceutical Sciences or equivalent Exp: 1+ years |
The Discovery Research team is looking for a highly motivated Research Associate/Associate Scientist to help with the discovery and development of GalXC-Plus™ RNAi therapeutics. This candidate will be responsible for helping prosecute in vivo and in vitro studies exploring the pharmacodynamics and efficacy for novel RNAi therapeutics and to advance the GalXC™ and GalXC-Plus™ platforms. The ideal candidate is a self-starter who is eager to learn, highly collaborative, and detail oriented. The successful candidate will be asked to carry out experiments and analysis in a manner reflecting an organization that demands scientific rigor and technical excellence with training and mentorship from a Scientist. Applicants interested in oligonucleotide therapeutics, gene therapy, or pharmaceutical sciences are encouraged to apply. | 5/11/2022 |
| 6877 | Dicerna Pharmaceuticals Lexington, MA Research Associate, RNAi Discovery Bachelor’s or Master’s Degree in Biology, Biochemistry or Pharmaceutical Sciences. Exp: 1+ years |
We are seeking a highly skilled BS/MS research associate to help in our drug discovery efforts. This is a hands-on research position that requires strong expertise in molecular and cellular methodologies. This is a full-time position. Dicerna offers an exciting work environment and strong team culture. Our company has a competitive benefits package and bonus incentive program. | 5/11/2022 |
| 6878 | Dicerna Pharmaceuticals Lexington, MA Research Associate/Associate Scientist, Discovery Research BS/MS in Biology, Biochemistry, Pharmaceutical Sciences or equivalent Exp: 1+ years |
The Discovery Research team is looking for a highly motivated Research Associate/Associate Scientist to help with the discovery and development of GalXC-Plus™ RNAi therapeutics. This candidate will be responsible for helping prosecute in vivo and in vitro studies exploring the pharmacodynamics and efficacy for novel RNAi therapeutics and to advance the GalXC™ and GalXC-Plus™ platforms. The ideal candidate is a self-starter who is eager to learn, highly collaborative, and detail oriented. The successful candidate will be asked to carry out experiments and analysis in a manner reflecting an organization that demands scientific rigor and technical excellence with training and mentorship from a Scientist. Applicants interested in oligonucleotide therapeutics, gene therapy, or pharmaceutical sciences are encouraged to apply. | 5/11/2022 |
| 6879 | Dicerna Pharmaceuticals Lexington, MA Research Associate/Senior Research Associate/Associate Scientist – Translational Biology Bachelor’s or Master’s Degree in Biology, Pharmacology or a related field Exp: 1+ year |
We are seeking a highly skilled research associate to lead mechanism of action and pharmacology studies on Dicerna’s GalXC therapeutics. Major responsibilities include conducting in vivo studies on our pre-clinical and clinical candidates and conducting hands-on research. You will apply your expertise on animal dosing and surgery and deep understanding of the molecular and cellular biology to study liver diseases and play an important role in all phases of drug discovery and clinical development at Dicerna. | 5/11/2022 |
| 6880 | DNA Diagnostics Center Fairfield, OH Clinical Scientist- Entry Level Biological Science Degree Required Exp: 1 year |
The Lab Technologist is responsible for the execution of a broad range of bench test procedures used in raw material qualification, and testing. In this position, you will work in a fast paced, customer focused, and challenging environment. Laboratory technologists assist with the receiving, labeling, testing and analyzing of samples in a sterile environment. They assist in the design and execution of laboratory testing according to standard procedures, as well as maintain accurate computer records of the process and results. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work as well as ability to work overtime and off-schedule days as needed. | 5/11/2022 |
| 6881 | DxTerity Los Angeles, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 5/11/2022 |
| 6882 | DxTerity Los Angeles, CA Research Associate B.S. or M.S Degree in Biochemistry, Molecular Biology or a related field Exp: 1-3 years |
DxTerity, a patient-centric genomics company located in Los Angeles, CA is looking to hire a Research Associate to join our Research and Product Development team. Responsibilities include: development of molecular diagnostic test kits, reagents and procedures in a team environment. Perform experiments independently after receiving general direction from supervisor. Make detailed observations, analyzes data and interpret results. Prepare technical reports, summaries, protocols and quantitative analyses. Maintain and develop skills in molecular biology and company technology through reading of internal reports and scientific literature. Support the achievement of project objectives and time schedules while meeting ISO and FDA regulatory and design control requirements. | 5/11/2022 |
| 6883 | Applied Medical Rancho Santa Margarita, CA Software Engineer I- Web Developer (Full Stack) BS in Computer Science, Computer Engineering, or related Exp: 0-2 years |
Responsibilities: Communicate with product experts, UI designers, and engineers to fully understand business requirements; Break down business requirements into clear and actionable tasks; Turn business requirements into clean, testable, and maintainable code; Collaborate with other engineers to implement, test, and deliver robust software | 5/1/2022 |
| 6884 | Applied Medical Rancho Santa Margarita, CA Process Development Engineer I- Surgical Simulations BS in Mechanical, Biomedical, Manufacturing Engineering, or related Exp: 0+ years |
In this role, the Surgical Simulation Process Engineer will work towards advancing the field of surgical training for residents and surgeons by sustaining and improving manufacturing processes as part of a cross-functional team. Research new manufacturing methods, technologies and materials. Develop and sustain existing manufacturing processes. Plan, organize, and qualify production lines for new products. | 5/1/2022 |
| 6885 | Applied Molecular Transport South San Francisco, CA Downstream Manufacturing Associate BS in Biology, Biochemistry, or related Exp: 0-3 years |
Responsibilities: Set-up and operation of single-use buffer preparation, tangential flow filtration (TFF), and chromatography equipment; Process monitoring and sampling, including performing routine sample analysis; Weigh out and dispense raw materials for preparation of buffers; Participation in daily operation and routine maintenance activities of process and analytical equipment; Maintain a clean and organized lab environment. | 5/1/2022 |
| 6886 | Applied Molecular Transport South San Francisco, CA Upstream Manufacturing Associate BS in Chemical Engineering, Microbiology, Biochemistry, or related Exp: 0-4 years |
Responsibilities: Set-up and operation of single-use fermentation, cell processing, and separation equipment; Process monitoring and sampling, including performing routine sample analysis; Weigh out chemicals, prepare media, solutions, and buffers; Participation in daily operation and routine maintenance of process and analytical equipment; Maintaining a clean and organized lab environment; Chemicals and consumables stocking, etc.; Maintaining strict adherence to batch records, SOP’s, and safety guidelines designate for the manufacturing process | 5/1/2022 |
| 6887 | Applied Molecular Transport South San Francisco, CA Research Associate I/II, Upstream Process Development BS or MS in Chemical Engineering, Microbiology, Biotechnology or related Exp: 1+ years |
We are seeking an experienced Research Associate I/II who will focus on small-scale expression and fermentation process development to produce novel biopharmaceutical proteins. Tasks may include: Transformations and working cell bank production; Small-scale evaluation in microtiter plate, flask experiments to support strain screening and fermentation development; Protein expression in 250mL to 30L; Cell lysis, wash, and inclusion body recovery. Hand-off to Downstream for purification; Sample preparation and analysis: gel electrophoresis, HPLC, Cedex BioAnalyzer, etc.; Assay development and protocol optimization | 5/1/2022 |
| 6888 | Applied StemCell Milpitas, CA Sales Associate BS in science Exp: 0-2 years |
Requirements: Ability to work independently and handle multiple projects simultaneously. Develops and manages a sales plan and strategy for assigned accounts and territory. Can multi-task in a demanding environment. The ability to understand the science behind our products/services and uses. Basic laboratory experience is a must, specifically for the applications in molecular cloning, genome editing, cell culture, stem cells / iPSCs, immune-oncology, animal modeling, and GMP/GLP process. | 5/1/2022 |
| 6889 | Aprecia Blue Ash, OH Quality Analyst I BS in science Exp: 0-3 years |
This position is primarily responsible for providing Quality support for manufacturing operations. Perform review and release of all manufacturing and packaging batch records, both in real time as batches are being manufactured and during final review of all associated batch documentation prior to batch release. Perform initial triage of deviation investigations that occur during batch manufacture, demonstrating the ability to understand complex quality issues. | 5/1/2022 |
| 6890 | Aquinnah Pharmaceuticals Cambridge, MA Research Associate MS in neuroscience, cell biology or related Exp: 1+ years |
This position is laboratory-based and requires strong experimental skills with a background in cell biology, molecular biology, or biochemistry. Under supervision, the candidate will assist in duties including, but not limited to: cell culture maintenance, compound screening, biochemical assays, immunocytochemistry, and analysis using state of the art high-content imaging. | 5/1/2022 |
| 6891 | Argonaut Manufacturing Services Carlsbad, CA Associate Scientist, Lyophilization BS in Biology, Molecular Biology, Computational Biology, Biochemistry or Bioengineering Exp: 1-5 years |
Assist in the development of client products for lyophilization – this includes designing, executing on experimental protocols and recording results, observations and ideas for improvement throughout the process; Work as part of a team to meet each project goal in a timely manner and communicating any delays to the appropriate person; Scale-Up R&D formulations and transfer them to Manufacturing/Production – being able to critically review a protocol and determine feasibility in Manufacturing/Production and make recommendations | 5/1/2022 |
| 6892 | Argonaut Manufacturing Services Carlsbad, CA Drug Product Manufacturing Associate I BS in Life Sciences or Engineering Exp: 1-2 years |
The purpose of this position is to perform tasks and operations relevant to the bulk formulation and/or filling operations required for sterile production of liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing. | 5/1/2022 |
| 6893 | Argon Medical Devices Athens, TX Manufacturing Engineer BS in Mechanical or Industrial Engineering Exp: 1-2 years |
Provide engineering support for the development and manufacture of Argon Medical Device products; Evaluate proposed designs for manufacturability; Recommend, develop and implement manufacturing related cost saving initiatives (Value Improvement Projects); Develop and implement process qualification protocols and reports; Perform root cause analysis of product/process issues and implement short and long-term corrective actions to improve product quality and reliability. | 5/1/2022 |
| 6894 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Microbiology Lab BS in Microbiology or related Exp: 0+ years |
Essential Functions: Media preparation; Glassware cleaning; Inventory / ordering; Lab cleaning and sanitization; Autoclaving various reagents and supplies; Assist laboratory personnel in daily activities to maintain high scientific quality and compliance with SOPs, protocols, and safety standards; Ability to wear, maintain, and properly use appropriate safety equipment, including, but not limited to eye protection, gloves, full face respirator, and lab coat; Adherence to all ARL Bio Pharma safety standards, policies, procedures, and protocols | 5/1/2022 |
| 6895 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Analytical Lab BS in Chemistry or related Exp: 0+ years |
Performs Thin Layer Chromatography and uses titration, refractive index, optical rotation and viscosity techniques; Works with UV-Vis, HPLC (High Performance Liquid Chromatography), GC (Gas Chromatography), FTIR, Microscopes, Balance, PH Meter, and Karl-Fisher titrator; Adhere to Quality Management System (QMS); Follow prescribed safety rules and regulations in performing all assigned duties | 5/1/2022 |
| 6896 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - R&D Lab BS in Chemistry or related Exp: 0+ years |
Responsibilities: Prepare chemical reagents/mobile phase; Assists chemical tracking/disposal; Assists sample retrieval, preparation and storage; Order and organize general lab supply; Wash glassware and maintain lab cleanness; Perform non-accredited laboratory tests; Adherence to all ARL safety standards, policies, procedures and protocols. | 5/1/2022 |
| 6897 | ARL Bio Pharma Oklahoma City, OK Chemist I - Analytical BS in Chemistry or related Exp: 1-2 years |
This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 5/1/2022 |
| 6898 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Chemistry Lab BS in Chemistry or related Exp: 0+ years |
This position is responsible for maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position is responsible for the daily calibration and/or verification of the balances and pH meter. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform limited tests under supervision. | 5/1/2022 |
| 6899 | Armata Pharmaceuticals Marina Del Rey, CA Research Associate I BS in Microbiology, Molecular Biology, Biochemistry, Cell Biology, Virology, Biological Sciences, or related Exp: 1+ years |
The Research Associate I position will support the research and development effort by performing in vitro microbiological and associated microbiology/molecular biology testing/analysis. Carry out microbiological, molecular and biochemical assays in collaboration with scientists and senior associates. Experience working with production and purification of recombinant proteins and/or antibodies, and analytic assays for characterization required. | 5/1/2022 |
| 6900 | Armata Pharmaceuticals Marina Del Rey, CA Research Associate I/II – Process Development BS or MS in Microbiology, Cell Biology, Chemistry, Chemical Engineering, Physical Chemistry or related Exp: 1+ years |
The Research Associate I/II position will support process development by assisting in upstream and downstream purification processes of bacteriophage. Experience working with and maintaining bacteria with excellent aseptic technique required. Hands on experience and knowledge of different types of purification systems (including: tangential flow filtration, AKTA chromatography systems) is required. | 5/1/2022 |
| 6901 | Arraystar Inc. Rockville, MD Lab Assistant - Molecular Biology BS in biological sciences Exp: 1-2 years |
Responsibilities: Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc.; Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines; Assist with the generation and updating of laboratory SOPs; Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. | 5/1/2022 |
| 6902 | Arthrex Ave Maria, FL Quality Assurance Specialist I - Sterilization BS in engineering, biology/microbiology, chemistry, toxicology or related Exp: 0+ years |
Responsibilities: Ensure proper and timely accurate completion of sterile load files of Arthrex Manufacturing Inc. products; Maintain the Sterile Release program for loads produced by Arthrex Manufacturing Inc. and ensure timely and safe product release to meet customer requests; Report and act by opening, disposition, evaluating, and closing on Non-Conformances observed during sterilization processes for Arthrex Manufacturing Inc. to provide a resolution for the disposition of affected loads. | 5/1/2022 |
| 6903 | Arthrex Pendleton, SC Environmental Engineer I BS in environmental engineering Exp: 1+ years |
The Environmental Engineer assists with technical and operational support under the guidance of the Environmental Engineer. Core objectives are to support each business location to meet the EPA’s regulations through waste stream determination, employee training, spill response, waste sample collection, chemical review and keeping adequate documentation. This position supports all areas of the Arthrex Environmental, Health and Safety Management System as needed. | 5/1/2022 |
| 6904 | Arthrex Naples, FL Engineer I - Packaging BS in packaging engineering or other engineering Exp: 0+ years |
Responsibilities: Coordinate Packaging Development activities for new MPI’s and product improvement projects; Ensure essential packaging development activities are completed prior to packaging design transfer activities; Provide support for packaging engineering related CAPA’s. | 5/1/2022 |
| 6905 | Arthrex Pendleton, SC Quality Engineer I BS in engineering or engineering technology Exp: 1+ years |
You will aid the Quality Supervisor to oversee, manage and provide direction to the QA departments that will effectively and profitably meet or exceed the internal and /or external client’s expectations by providing superior quality products and service. You will be responsible for working with Design and Manufacturing Engineering to prevent quality discrepancies and help determine the root cause and drive corrective action with the guidance of Quality Engineers. | 5/1/2022 |
| 6906 | Anika Sarasota, FL Quality Engineer I BS in Mechanical or Biomedical Engineering Exp: 0+ years |
This position works collaboratively with the product development team to evaluate product designs for manufacturability. Evaluate product design features to determine appropriate tolerances, manufacturing requirements, measurement methods and acceptance criteria. | 5/1/2022 |
| 6907 | Arvinas New Haven, CT Associate Scientist/Senior Associate Scientist (Collaborations) MS in Biology or related Exp: 1+ years |
This position is laboratory-based and requires strong experimental skills, and the ability to effectively partner with team members in order to deliver quality data in support of drug discovery efforts. Key responsibilities of this role include: Design and execute experiments, and perform data analysis; Sterile technique and experience culturing cancer cell and immune cell lines; Perform cellular functional assays | 5/6/2022 |
| 6908 | Arvinas New Haven, CT Associate Scientist, Immunology and Immuno-oncology MS in Biology or related Exp: 1+ years |
This position in the Immuno-Oncology Group (IO-IMM) at Arvinas is laboratory-based and requires strong experimental skills, and the ability to effectively partner with team members in order to deliver quality data in support of early drug discovery efforts. Key responsibilities of this role include: Design, execution, and data analysis of experiments; Utilize appropriate methodologies (tool compounds, genetic knockdown, etc.) to characterize target of interest function, pathway modulation, and cell sensitivity | 5/6/2022 |
| 6909 | Arvinas New Haven, CT Research Associate, Platform Biology BS in Biology, Biochemistry, or related Exp: 0+ years |
This key position in our functional area support team (FAST) within the platform biology group will support the discovery and characterization of PROTACs (Proteolysis-targeting chimeras) and related molecules for Arvinas research programs. This position is laboratory-based and requires strong experimental skills, and the ability to effectively partner with team members to deliver quality data in support of early drug discovery efforts | 5/6/2022 |
| 6910 | AssayGate Ijamsville, MD Associate Scientist BS or MS in Biology or related Exp: 1+ years |
You will be responsible for lab testing of both bead and planar protein microarrays. You will plan, coordinate and exercise studies toward optimization of multiplexing protein assay conditions. In addition, you will plan, develop and communicate concepts for reducing costs and improving assay efficiencies | 5/6/2022 |
| 6911 | Atalanta Therapeutics Boston, MA Data Engineer - Bioinformatics MS in bioinformatics, computer biology, or related Exp: 0+ years |
As part of the bioinformatics team, the successful candidate will help develop solutions for drug discovery efforts. They will bring rigor and innovation to drive cloud-based software development to accelerate multiple parts of drug discovery such as target prioritization, drug design, and drug characterization. Some experience in building dashboards is required to develop meaningful tools that makes data accessible for users of all levels. The candidate will learn about common bioinformatics file formats and will be trained to integrate data using open-source tools to accelerate the drug discovery activities. | 5/6/2022 |
| 6912 | Atalanta Therapeutics Boston, MA Associate Scientist/Senior Associate Scientist, Bioinformatics MS in bioinformatics, computer biology, or related Exp: 0+ years |
The successful candidate will have the opportunity to learn bioinformatics skills to perform cutting-edge drug discovery. The candidate’s biological foundation and experience with known bioinformatics databases will enable bioinformatics analysis of drug targets, drug design and drug characterization. Some hands-on experience analyzing next-generation sequencing data and knowledge of biology or molecular biology is required for this role. The candidate will be supporting multiple drug development programs for difficult to treat neurodegenerative diseases. | 5/6/2022 |
| 6913 | Atalanta Therapeutics Boston, MA Associate Scientist/Senior Associate Scientist, In Vivo Pharmacology BS or MS in related science or engineering field Exp: 1+ years |
The Associate Scientist/Senior Associate Scientist will be responsible for assay development and execution of experiments to determine the biodistribution, pharmacodynamic properties and efficacy of oligonucleotides in research and preclinical studies supporting multiple drug discovery programs and platform discovery research. | 5/6/2022 |
| 6914 | Atalanta Therapeutics Boston, MA Associate Scientist/Senior Associate Scientist, Oligonucleotide Chemistry BS or MS in Chemistry Exp: BS: 1+ years; MS: 0-2 years |
Successful candidates will have experience with modern laboratory equipment, and spectroscopic analysis, preferably in relation to oligonucleotides, as well as demonstrated ability to work as part of an integrated team on multiple parallel projects. This individual will be responsible for the independent operation and maintenance of instruments to synthesize, purify, and analyze chemically modified oligonucleotides as well as prepare samples for in vitro and in vivo studies. | 5/6/2022 |
| 6915 | Atara Bio Denver, CO Research Associate, Process Sciences BS in relevant science Exp: 0+ years |
This position will be responsible for cell culture, analytical cell reagent preparation, and stocking and maintaining the PD laboratories. Under minimal supervision, the successful candidate is expected to assist in experiments, carefully document method and materials, and communicate findings. | 5/6/2022 |
| 6916 | Athenex Clarence, NY Microbiology Technician (2nd Shift) BS in Microbiology or Biology Exp: 0 years |
Responsibilities include: Perform environmental monitoring of ISO5/ISO7/ISO8 manufacturing areas (viable air, viable surface, and non-viable particulate) as well as inspection for compliance; Complete accurate and legible written data entry on records and documents for tests performed; Accurate computer data entry, trending, and presentation; Support Media Fill Validations, Engineering Validations and Cleaning Validations; Collection and testing (Bioburden/TOC/Conductivity) of water samples throughout the facility | 5/6/2022 |
| 6917 | Atreca San Carlos, CA Research Associate I, Protein Engineering BS or BA in Bioengineering, Chemical Engineering, Biology, Biochemistry, Biotechnology, or related Exp: 0-5 years |
The successful candidate will become a key member of our protein pipeline team, supporting production and characterization of antibodies, proteins, and engineered bispecifics. This position will have the opportunity to learn and contribute to development and testing of novel antibody-based therapeutics. | 5/6/2022 |
| 6918 | AtriCure Pleasanton, CA Associate R&D Engineer MS in Mechanical or Biomedical Engineering, or Life Sciences Exp: 1+ years |
This position will contribute to the research and development of the next generation of AtriCure products including RF, cryo and LAA management and potential adjacent therapies and technologies new to AtriCure. Beyond displaying knowledge of core engineering and scientific principles, this position requires excellent teamwork, communication, curiosity and organizational skills to assist us in growing our business. The person in this position will work within a project team environment to develop novel and/or next generation medical devices used by cardiologists, electrophysiologists, and cardiac surgeons. | 5/6/2022 |
| 6919 | AtriCure Mason, OH Quality Technician BS or Associates in science Exp: 1-3 years |
The Quality Technician is responsible for a variety of activities to support the Quality department such as providing support to quality engineering and inspection as needed, partnering with manufacturing with daily production needs, and ensuring compliance to domestic and international regulatory requirements. | 5/6/2022 |
| 6920 | August Bioservices Nashville, TN Manufacturing Technician I – Filling, Lyophilization, & Terminal Sterilization BS or Associates in science Exp: 0-1 years |
Responsibilities: Support and operate processing equipment in accordance with SOPs, in classified areas; Actively participate in troubleshooting processes and equipment problems as well as assisting the manager in completing all necessary paperwork associated with investigations, deviations, and remarks; Use proper aseptic technique while performing tasks to set up filling line equipment including; vial / syringe fillers, lyophilizer loading system, capper and tray loader, parts / terminal sterilizers | 5/6/2022 |
| 6921 | Avance Biosciences Houston, TX Laboratory Associate II BS in Biological Sciences Exp: 1+ years |
Responsibilities: Carry out Molecular Biology, Microbiology, Protein experiments following established SOPs and/or guidance of laboratory management; Perform DNA/RNA extraction, quantification, and gel QC; Perform PCR setup for qualitative and quantitative analysis; Report experimental results to project managers in a timely manner; Follow established quality management policies and GLP and GMP practices | 5/6/2022 |
| 6922 | Avantor Morrisville, NC Process and Validation Engineer BS in Industrial, Chemical, or Mechanical Engineering, or related Exp: 1+ years |
Responsible for multiple phases of manufacturing processes and process improvement projects. Implements process improvements to meet quality standards, designs and conducts feasibility studies, and solves problems. Develops and executes validation of equipment and processes. Creates necessary documentation and aides in communication to personnel. Serves as a resource to site associates and coordination of work within the scope of assigned projects. | 5/6/2022 |
| 6923 | Regeneron Tarrytown, NY Temp Research Associate, Auditory, Molecular Biology B.S. Exp: 0-4 years |
We are seeking a talented, creative Research Associate to join Regeneron’s Auditory research team. You will be involved in basic research studies designed to understand and treat the biology behind various forms of deafness and hearing impairment. The group is working towards genetic therapies to treat these disorders. | 5/3/2022 |
| 6924 | Regeneron Tarrytown, NY Laboratory Assistant I Bachelor's degree Exp: 0-1 years' |
Our Clinical Bioanalysis group is seeking a highly motivated Laboratory Assistant I to provide bioanalytical laboratory support under the direct supervision of Management, following appropriate company SOPs and regulations to carry out assigned tasks. Maintains laboratory organization and inventory of reagents/supplies as well as a clean and orderly work area to support all nonclinical and clinical development programs. May perform bioanalytical experiments under the direct supervision of a manager. | 5/3/2022 |
| 6925 | Regeneron Tarrytown, NY Temp - Research Specialist, Bioanalytical and Biomarker Technology MS Exp: 0-3 yrs |
Regeneron is looking for a highly motivated R&D Specialist to conduct research in our state-of-the-art facilities and technology to perform qualitative and quantitative mass spectrometry experiments focusing on autoimmune, infectious disease and oncology targets. In this role, you will utilize the latest mass spectrometry techniques for the discovery and validation of novel viral- and cancer-specific antigens from human tissues and cell lines as well as to develop innovative techniques and investigate new technologies to enhance our target discovery efforts. | 5/3/2022 |
| 6926 | Regeneron Tarrytown, NY R&D Associate, Genome and Protein Engineering Technologies BS/MS Exp: 1-2 years |
The Genome Engineering Technologies group is currently seeking a curious and motivated Research Associate to join our team. The successful candidate must have previous mouse handling experience and strong interest in expanding in vivo skills as the role will lend in vivo support to multiple projects including lysosomal diseases, next-generation protein, gene, and cell therapies, and general technology development of novel biologics and mechanisms of action. | 5/3/2022 |
| 6927 | Regeneron Tarrytown, NY R&D Associate, Nucleic Acid Therapeutics BS/MS in molecular biology, biochemistry, bioengineering or related field Exp: 1-3 years |
VelocImmune (VI) Next is an innovative group that focuses on development of groundbreaking technologies and platforms. The nucleic acid therapeutics group under VI-Next is seeking a highly skilled and motivated researcher to support nucleic acid therapeutics development efforts across Regeneron. Major responsibilities in this position will include (but not limited to): production, purification, and characterization (expression, stability, purity, and immunogenicity) of mRNA candidates, screening siRNA/ASO and support other technology development efforts. This group comprises of 3 teams working on various other nucleic acid therapeutic modalities, and the role will provide an opportunity to overlap and learn about various oligo therapy modalities. | 5/3/2022 |
| 6928 | Regeneron Tarrytown, NY R&D Associate, Protein Biochemistry BS or MS in Biophysics, Biochemistry, Chemical Engineering or related field Exp: 0-2 years |
Regeneron's Protein Biochemistry group, located in Tarrytown NY is seeking an R&D Associate or R&D Specialist who will provide in-depth characterization of therapeutic proteins to support research, develop-ability assessments, and early development programs through IND. In this role you will be encouraged to conduct method development and technology innovation efforts aimed to improve our understanding of biotherapeutic proteins and specifically address both upstream research and late-stage program needs. | 5/3/2022 |
| 6929 | Cellular Dynamics [FUJIFILM] Madison, WI Research Specialist - Assay Development Group - (#368) Bachelor’s degree in biomedical engineering, stem cell biology, cell biology, developmental biology, immunology, or a closely related scientific fiel Exp: 0-1 year |
FUJIFILM Cellular Dynamics, Inc in Madison, WI is recruiting for a Research Specialist to support our FCDI R&D Assay Development group. This position requires a self-motivated individual with experience in cellular and molecular biology who can contribute to our efforts to eventually expand assays across all FCDI platforms. Qualified individuals need to be inspired to support the development of not only assays for our therapeutics and discovery research products but help build structure to the newly formed FCDI Assay Development team. We provide development and support to enhance your career using cutting edge iPSC technology. In this role you will provide technical support for developing custom assays to evaluate the quality, purity and performance of FCDI iPSC-derived products. This position supports the development and optimization of cell-based assays using cell imaging and gene expression tools and instruments including, but not limited to flow cytometry, microscopy and PCR. | 5/4/2022 |
| 6930 | Cellular Dynamics [FUJIFILM] Madison, WI Research Specialist - Process Engineering - (#370) Bachelor’s degree in chemical or bio-engineering, stem cell biology, cell biology, developmental biology, immunology or a closely related scientific f Exp: 0-1 year |
We are recruiting for a Research Specialist - Process Engineering to support our continued growth and on-going development projects. Qualified individuals need have the capability, and to be inspired to support the development of therapeutics (cGMP) products and tools to support research endeavors. We aspire to improve the quality of life through our efforts. In return we provide development and support to enhance your career using cutting edge iPSC technology. In this hands-on laboratory role - you will focus on the scale-out, scale-up, optimization, and characterization of bio-processes for pluripotent stem cell expansion and directed differentiation of pluripotent cells to terminally differentiated cells. Design and execute experiments involving bioreactors, volume reduction technologies, and fill/finish operations. Write protocols and reports and contribute to the tech transfer of bio-processes to manufacturing. | 5/4/2022 |
| 6931 | Cellular Dynamics [FUJIFILM] Madison, WI Process Engineer - Manufacturing Science and Technology - (#388) Bachelor’s degree in chemical or bio-engineering, chemistry, biology, biochemistry, immunology or a closely related scientific field. Exp: 0-1 year |
We are recruiting for a Process Engineer - Manufacturing Science and Technology to support our continued growth and on-going development projects. Qualified individuals need to be inspired to support the development of therapeutics and life science products and tools to support research endeavors . We aspire to improve the quality of life through our efforts. In return we provide development and support to enhance your career using cutting edge iPSC technology. In this role you will focus on improving process consistency, increasing scale, and reducing cost of goods of bio-processes for manufacturing iPSC-derived research and therapeutic products. This is a hands-on laboratory role working on the scale-out, scale-up, optimization, characterization and troubleshooting of bioprocesses for iPSC expansion and directed differentiation to terminally differentiated cells. Design and execute experiments involving new media, 2D and 3D vessel types, cell harvest technologies, and fill/finish operations. Write protocols and reports and contribute to the technology transfer of bioprocesses to manufacturing. | 5/4/2022 |
| 6932 | Steris St. Louis, MO Associate Scientist I Bachelor degree in Biology, Microbiology, Molecular Biology, Biochemistry, or Chemistry is preferred. Exp: 0-5 years |
Responsibilities Carries out assigned projects, laboratory work, and data analysis under the direction of a supervisor Operates and maintains laboratory equipment Works under supervision with direct instructions. Carries out routine and semi-routine tasks independently. Understands and complies with accepted laboratory and safety procedures. Demonstrates excellent laboratory technique | 5/4/2022 |
| 6933 | West Pharma Exton, PA Associate Scientist, Lab, CCI BS in Chemistry or related technical degree. Exp: 0-3 years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment. | 5/4/2022 |
| 6934 | West Pharma Exton, PA Associate Scientist, Lab, 2nd Shift BS in Chemistry or related technical degree. Exp: 0-3 years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment. This role will be 2nd shift work. | 5/4/2022 |
| 6935 | West Pharma Scottsdale, AZ Associate Engineer Bachelor’s degree in engineering or laboratory discipline Exp: 0-3 years |
In this role, the Associate Lab Engineer will work under the direction of the Lab Supervisor to assist with test equipment qualifications, test fixture/jig design, test method development, and test method validations. This individual will bring excellent analytical, engineering, and organizational talent to the execution of development projects at West. | 5/4/2022 |
| 6936 | West Pharma Exton, PA Bioanalytical Chemist, Point of Care Diagnostics Master’s in a scientific or engineering discipline. Exp: 1-2 years |
The Applied Research & Technology Scouting (AR&TS) team within West is responsible for driving the future of the company by identifying and developing innovative products designed to improve patient lives. This objective will be accomplished through a mix of internal organic research and external inorganic collaboration. The inorganic effort will span early-stage academic research to more established technologies in the private sector. The inorganic effort will seed the organic efforts. The scope encompasses technology fields that are adjacent to and transformational to West’s core products. The role will work within the recently established Diagnostic Research & Detection Technology team to identify and evaluate technologies and concepts in a broadly defined Biosensor space. The team’s output will feed the development of new products and serve new markets. The timeline for realization of the products is within a 5-year time horizon. Internal to West this team will collaborate with teams focused on drug delivery and novel therapies. External to West the team will be interfacing with researchers from academic institutions translating potential value-adding technologies, through feasibility and into reality. Projects will focus on technology validation and integration. This will require the planning and performing of experiments, designing test equipment and prototypes, and integrating different principles of optical, mechanical, and electronic engineering. | 5/4/2022 |
| 6937 | Cell Signaling Technology Danvers, MA Research Associate BA, BS, or MS degree in a biological science Exp: 1+ years' |
Our team is growing, and we are looking for a talented, highly motivated, and detail-oriented Research Associate for a position within our Proteomics Group. You will support sample preparation for LC-MS/MS analysis and should possess strong organizational skills and exceptional attention to detail. While the primary responsibility of this role is processing samples to be run on the mass spec, you will have plenty of opportunity to participate in other projects within the Proteomics team, including instrument operation, data analysis, method development, and research projects. | 5/5/2022 |
| 6938 | Cell Signaling Technology Beverly, MA Research Associate, Antibody Purification Bachelors degree in a biological science (e.g. molecular biology, cell biology, biochemistry or biotechnology) Exp: 1 years |
Work in the lab under supervision of manager to aid in the production and/or purification of polyclonal and monoclonal antibodies. A research associate will work closely with team members and manager to ensure work is completed to internal customer’s satisfaction with respect to quality and timeline. | 5/5/2022 |
| 6939 | Cell Signaling Technology Danvers, MA Research Associate I - Peptide Synthesis Bachelor's degree in Chemistry or Biology Exp: 0-2 years' |
A successful Research Associate I will contribute to a highly efficient, cohesive team that satisfies the peptidyl needs of the Product Development process and other groups throughout the company, is comfortable working independently in a high throughput production environment with a repeating weekly work schedule, and demonstrates a drive for innovation in order to change or improve work processes. | 5/5/2022 |
| 6940 | Civetta Therapeutics Cambridge, MA Cell Biology Research Associate BS in Biology, Molecular Biology, Biochemistry, or related Life Science discipline Exp: 1-3 years |
We are seeking a highly-motivated Research Scientist to help support our chemical biology efforts at Civetta. This candidate will help us discover small molecule modulators of beta-propeller proteins, support validation of new targets, and help propel our ongoing drug discovery programs. This is an excellent opportunity for individuals looking to work in a fast-paced, dynamic biotech environment. | 5/5/2022 |
| 6941 | Jounce Therapeutics Cambridge, MA Research Associate / Senior Research Associate, Discovery B.S./M.S. in biology, biochemistry, immunology or related discipline Exp: 1+ years |
Jounce is looking for a Research Associate/Senior Research Associate Scientist with a strong scientific curiosity to support in vitro efforts in Target Identification and Validation group of our Discovery Immuno-Oncology Team. The successful candidate will be a highly motivated bench scientist committed to elucidating the mechanism of action, and enabling the development, of novel cancer immunotherapeutic biologics. They will generate data to support key decisions for project teams and actively participate in the interpretation of data and design of experiments. They will have the opportunity to work independently and collaboratively to advance portfolio programs in a dynamic and fast-paced environment. | 5/5/2022 |
| 6942 | Repligen Waltham, MA Sustaining Mechanical Engineer - Life Sciences BS or MS degree in an engineering field Exp: 1-3+ years |
Repligen is seeking a Product Engineer - II to join the product engineering team in the R&D group. This successful candidate should have some device-oriented product development experience and a willingness to work with and contribute to a group environment. The group work will involve other engineers and scientists from R&D as well as individuals from Manufacturing, Quality, and Process Engineering. The ideal candidate is an experienced engineer, capable of overseeing both the implementation of design and process changes, driving changes towards continuous improvement, as well as maintaining existing manufacturing documentation. | 5/5/2022 |
| 6943 | BioMarin Novato, CA RESEARCH ASSISTANT/RESEARCH ASSOCIATE Bachelor's degree in a scientific discipline or equivalent or Master's degree Exp: BS: 0-5+ years; MS: 0-2+ years |
This laboratory based position in Manufacturing Science and Technology (MSAT) requires technical expertise in protein characterization and purification systems in support of ongoing manufacturing operations. He or she participates in monitoring and troubleshooting existing processes to build a detailed process understanding and developing process improvements consistent with cGMP. This position involves collaboration with process development, manufacturing, quality control, and quality assurance groups. Travel is limited to attending relevant professional conferences and workshops. | 4/25/2022 |
| 6944 | BioMarin Petaluma, CA RESEARCH ASSISTANT, VIVARIUM - BIOLOGY RESEARCH bachelor’s degree in a relevant scientific discipline Exp: 0-2 years’ |
We are currently seeking a qualified and motivated individual to join our team in Model Development as a Research Assistant. The selected individual will perform routine duties associated with the husbandry of mouse and rat colonies in a research laboratory setting and will be involved in aspects of in-vivo research in support of efficacy studies. | 4/25/2022 |
| 6945 | Bristol Myers Squibb Summit, NJ Assistant / Associate / Senior Associate Scientist, Biologics Manufacturing – Upstream Operations Biochemistry, Bioengineering, Biochemical, Chemical Engineering or related discipline. Assistant Scientist - BA/BS; Associate Scientist –MA/MS . Exp: BS: 0-2 yrs; MA/MS: 0-2 years |
We are currently looking for an Assistant Scientist, Associate Scientist OR Senior Associate Scientist to join our Biologics Manufacturing Team within the BMS’s Biologics Development & Manufacturing group in Summit, New Jersey. As a member of the Biologics Development & Manufacturing group, the Assistant / Associate / Senior Associate Scientist will provide technical and operational expertise and oversight to early stage clinical manufacturing campaigns. The focus of this position will be on upstream operations and support of downstream operations in single-use manufacturing environment. | 4/26/2022 |
| 6946 | Bristol Myers Squibb Summit, NJ Associate Scientist, Biologics Manufacturing – Downstream Operations Biology, Biochemistry, Bioengineering, Biochemical, Chemical Engineering or related discipline. Assistant Scientist - BA/BS; Associate Scientist – MA/ Exp: BS: 0-2 yrs ; MA/MS: 0-2 years |
We are currently looking for an Assistant Scientist, Associate Scientist OR Senior Associate Scientist to join our Biologics Manufacturing Team within the BMS’s Biologics Development & Manufacturing group in Summit, New Jersey. As a member of the Biologics Development & Manufacturing group, the Assistant / Associate / Sr. Associate Scientist will provide technical and operational expertise and oversight to early stage clinical manufacturing campaigns. The focus of this position will be on downstream operations and support of upstream operations in single-use manufacturing environment. | 4/26/2022 |
| 6947 | Bristol Myers Squibb Seattle, WA Research Associate, Cell Therapy BS in a scientific discipline Exp: 1-3 years |
In this individual contributor, lab-based role, the Research Associate will work in a collaborative environment to perform process analytics testing to support BMSs development programs. This position will report to an Analytical Core Team Lead, joining a subgroup within Analytical Operations. The incumbent will be part of an analytical testing group that values data quality, high productivity, and teamwork. | 4/26/2022 |
| 6948 | Bristol Myers Squibb Seattle, WA Research Associate BS in a scientific discipline Exp: 1-2 years |
In this individual contributor, lab-based role, the Research Associate will work in a collaborative environment to perform product characterization testing to support clinical programs. This position will report to the head of Clinical Product Characterization (CPC). The incumbent will join a clinical testing group that values data quality, high productivity and teamwork. | 4/26/2022 |
| 6949 | Bristol Myers Squibb Seattle, WA Research Associate, Cell Core - Cell Therapy B.S. in Biology, Chemical Engineering, Bioengineering or relevant scientific discipline Exp: 0-2 years |
The Research Associate will additionally assist in manufacturing engineered T-cell products and intermediates in support of Research, Technical Development, Process Development, Analytical Development, and Process Characterization efforts. The position will require experimental execution, documentation, data analysis, drafting of technical reports, and presentation of results. Strong attention to detail and flexibility to work evening and weekend shifts is required. | 4/26/2022 |
| 6950 | Bristol Myers Squibb Seattle, WA Research Associate, Viral Vector and Gene Delivery Process & Analytical Development B.S. in Biology, Bioengineering, Biochemistry, or related discipline Exp: 0-2 years |
We are seeking an enthusiastic, self-driven individual to join the Gene Delivery Process & Analytical Development team as a Research Associate. | 4/26/2022 |
| 6951 | Emergent Biosolutions Gaithersburg, MD Associate Scientist I B.S. in biology, biochemistry, engineering or related discipline Exp: 0-3 years |
The Associate Scientist I will be a member of Drug Substance department within Development Services focused on Upstream Process Development. Contribute to the logistics/planning/execution of experiments for the Drug Substance Support Team activities. | 4/28/2022 |
| 6952 | Exact Sciences Cambridge, MA Research Associate I - Protein - Temporary Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
We are seeking a talented and motivated Research Associate to join the Protein Biomarker Development team within our Multi-Cancer Early Detection program. This position will support the development and validation of protein assays from the feasibility stage through commercialization, in addition to the processing and screening of samples and specimens. The candidate will work closely with the sample processing, assay development, automation, and data science teams to support the product development efforts towards potential diagnostics assays. | 4/28/2022 |
| 6953 | Exact Sciences Cambridge, MA Research Associate I - Protein Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
We are seeking a talented and motivated Research Associate to join the Protein Biomarker Development team within our Multi-Cancer Early Detection program. This position will support the development and validation of protein assays from the feasibility stage through commercialization, in addition to the processing and screening of samples and specimens. The candidate will work closely with the sample processing, assay development, automation, and data science teams to support the product development efforts towards potential diagnostics assays. | 4/28/2022 |
| 6954 | Exact Sciences Madison, WI Research Associate II, Product Development Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day-to-day experimentation and is responsible for the execution of bench experiments and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 4/28/2022 |
| 6955 | Exact Sciences Redwood City, CA Associate Histotechnologist ($3,000 sign-on bonus!) - Monday - Friday, 12:00pm - 8:30pm Shift Bachelor’s Degree in Life Sciences, or field as outlined in the essential duties. Exp: 1+ years |
The Associate Histotechnologist will perform skilled and accurate cutting on patient specimens under the supervision of pathologists, interact with sending sites and ordering physicians, perform quality control and specimen-related checks, and comply with all applicable local, state, and federal laboratory requirements. | 4/28/2022 |
| 6956 | Exact Sciences Redwood City, CA Associate Histotechnologist ($3,000 sign-on bonus!) - Monday-Friday, 7:00am - 3:30pm Shift Bachelor’s Degree in Life Sciences, or field as outlined in the essential duties. Exp: 1+ years |
The Associate Histotechnologist will perform skilled and accurate cutting on patient specimens under the supervision of pathologists, interact with sending sites and ordering physicians, perform quality control and specimen-related checks, and comply with all applicable local, state, and federal laboratory requirements. | 4/28/2022 |
| 6957 | Exact Sciences Redwood City, CA Associate Histotechnologist I, AM Shift - $3,000 sign-on bonus! Bachelor’s Degree in Life Sciences, or field as outlined in the essential duties. Exp: 1+ years |
The Associate Histotechnologist will perform skilled and accurate cutting on patient specimens under the supervision of pathologists, interact with sending sites and ordering physicians, perform quality control and specimen-related checks, and comply with all applicable local, state, and federal laboratory requirements. | 4/28/2022 |
| 6958 | Eli Lily New York, NY Research Associate, Preclinical R&D Masters Exp: 1+ years |
The Research Associate will support the validation of novel therapeutic candidates by performing hands-on, bench-level research involving both cell culture and tissue-based experiments, as well as sample processing and analyses from in vivo animal studies. The successful candidate will work with the Preclinical R&D team to coordinate in vivo studies with contract research organizations (CROs) and manage sample inventory. The ideal candidate will be a team player, with strong organizational, interpersonal, and communication skills. | 4/28/2022 |
| 6959 | Eli Lily Branchburg Township, NJ Research Associate-QC Biochemistry BS, MS in a related science (e.g., Chemistry, Biochemistry) Exp: BS: 0-5 years; MS: 0-2 years |
Conduct routine and non-routine analyses of in-process materials, raw materials, finished goods, and stability samples by appropriate biochemical methods as assigned by Supervisor. Performs routine QC responsibilities as needed. May lead projects such as method validation activities. Applies acceptable cGMP practices during execution of all work tasks. Works independently with moderate supervisory guidance. | 4/28/2022 |
| 6960 | Eli Lily Pasadena , CA Research Associate, Chemistry/Biochemistry Undergraduate degree in chemistry, biochemistry, chemical engineering Exp: 1+ years |
The team at Protomer is working on responsive biotherapeutics that can be controlled using small molecule modulators. Protomer team is based in Pasadena and the research labs are located in Pasadena. We are currently expanding the team to advance several programs, including glucose sensing insulins (GSIs), and are looking for a research associate with experience in biochemistry, synthesis, bioconjugations, and purification/characterization of therapeutic compounds of interest. The ideal candidate will have a bachelor’s or master’s degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a team player in a fast-paced research setting. The applicant will be responsible for assisting Protomer’s senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively participate and present in team meetings and is expected to contribute to the team’s progress and success. | 4/28/2022 |
| 6961 | Meridian Medical Technologies [Pfizer] Pearl River, NY Associate Scientist - mRNA Molecular Biology MS in Molecular Biology, Cell Biology, Virology, or a related scientific field. Exp: 0-2 years |
The Pfizer Viral Vaccines group is seeking an Associate Scientist to join our highly dynamic team in support of multiple vaccine research and development programs, including the preclinical evaluation and early clinical development of our mRNA-based vaccine platforms. The incumbent will be supporting activities related to mRNA optimization, production and characterization, including but not limited to: Standard molecular biology techniques, in-vitro mRNA transcription, capping and in-vitro characterization using cell-free/cell-based assays, with the aim of optimizing vaccine design strategies. The successful candidate will be part of a very collaborative team and should possess a strong work ethic, be dependable and adaptable to fast-paced environments. | 4/28/2022 |
| 6962 | Precision for Medicine [Precision Medicine Group] Houston, TX Technologist I - Laboratory Bachelor’s Degree (Medical technology, Life Sciences, Biology, or other related discipline) Exp: 0 - 2 years |
Participate in Flow. PBMCs, IF / IHC projects through assay development, validation, and execution in a timely manner. Process clinical samples. Perform assays according to SOPs and support development of new procedures and improvement of existing SOPs. May perform other cell-based assays. | 4/28/2022 |
| 6963 | AlphaGenesis Yemessee, SC Veterinary Technician BS in Veterinary Science (preferred) Exp: 0+ years |
Under the direction of veterinary staff, maintain and monitor the health and physical environment of Charles River or external customer animals involving complex instructions and requiring technical expertise. Assist veterinary staff in the documentation and triage of all laboratory animal health cases. | 4/25/2022 |
| 6964 | Alpine Immune Sciences Seattle, WA Bioanalytical Research Associate BS or MS in Bioanalytical Chemistry, Biochemistry, Biology or related Exp: 1 year |
This individual will be responsible for bioanalytical assay development and biological sample analysis to support our protein-based immunotherapeutic platforms from discovery and late stage research into clinical development. The successful candidate must have some experience with ELISAs and related bioanalytical assays. Excellent written and oral communication skills, as well as strong organizational skills are essential. | 4/25/2022 |
| 6965 | Alpine Immune Sciences Seattle, WA Pharmacokinetic Associate / Scientist MS in pharmacology, pharmacokinetics, pharmaceutical science, bioengineering, chemical engineering, or related Exp: 0-2 years |
This individual will support the development of novel drug candidates by design, analysis, and interpretation of non-clinical and clinical pharmacokinetic (PK) and pharmacokinetic/pharmacodynamic (PK/PD) studies. The successful candidate must have experience in the field of drug discovery or development or relevant area of expertise. Excellent written and oral communication skills, as well as strong organizational skills are essential. | 4/25/2022 |
| 6966 | Alstem Richmond, CA Research Associate BS or MS degree in Biochemistry, Molecular Biology or related Exp: 1+ years |
The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. Minimum 1 year of experience in a cell culture setting after graduation. | 4/25/2022 |
| 6967 | Alumis South San Francisco, CA Clinical Trial Associate BS in biological/life sciences or health care management, or a BSN Exp: 1-2 years |
You will work closely with the Clinical Operations team to support the full scope of study activities, including site activation, patient recruitment, study monitoring and site and vendor management on Phase 1 to Phase 3 trials. You will work cross functionally within the Alumis team as well as with study sites, CROs and other vendors. Responsible for site feasibility and recruitment, including review of Site Information Questionnaires. | 4/25/2022 |
| 6968 | Alveo Alameda, CA Assay Development and Verification Scientist I BA or BS in Biochemistry, Molecular Biology, Microbiology or related Exp: 1-3 years |
You Will: Assist senior staff with execution of strategic initiatives for the Assay Development R&D group; Conduct technical experiments to develop sample-to-answer molecular diagnostics assays under strict project timelines; Maintain, control and propagate an exceptional quality of the documentation and analysis of results that will be submitted to regulatory agencies; Proactively identify and escalate product risks and issues to their manager and relevant stakeholders | 4/25/2022 |
| 6969 | Alveo Alameda, CA Quality Control Analyst I BS in Biology, Chemistry, Molecular Biology, or related Exp: 1+ years |
You Will: Perform automated and manual assays as detailed in established SOPs and QC test method procedures, including raw material, in-process and finished product; Interpret test results against specifications to support material dispositioning; Perform procedures to formulate liquid chemical and biological solutions for use as controls during testing; Prepare and inspect equipment for use in chemical and bio-formulations, such as pumps, filters, tubing connections and mixers | 4/25/2022 |
| 6970 | Alvogen Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related Exp: 0-3 years |
Responsibilities: Perform job functions in a safe manner consistent with site safe practices and regulatory (e.g. – OSHA) requirements. Conduct assigned tasks in compliance with cGXP requirements, current industry standards, compendia standards, FDA expectations and internal procedures. Perform routine sample analysis requiring general laboratory skills such as weighing, pipetting, titration, and basic operation of laboratory instrumentation. Perform analysis with a practical understanding of the test procedure and instrument operation. | 4/25/2022 |
| 6971 | Amador Bioscience Remote, MD Associate Scientist /Senior Associate Scientist- Bioanalysis & Biomarkers BS or MS in biology, immunology, chemistry, pharmacology, or related Exp: 1-3 years |
Responsibilities: Assist in developing, validating, and conducting bioanalytical methods (LBA and/or cell-based assays) for biological sample testing, data QC, and data reporting; Set day-to day objectives, perform complex tasks and novel procedures, communicate results to supervisor in a timely manner; Complete all records thoroughly and accurately for QA/QC and GxP purposes using Good Documentation Practices; Ensure lab maintenance activities and maintains a clean and safe lab environment | 4/25/2022 |
| 6972 | NSF International Ann Arbor, MI Technician II - Exposures Lab BS or Associates in science (preferred) Exp: 1-5 years |
Perform laboratory procedures following defined processes and standard operating procedures to support product certification. Technician will be involved in exposure of water system components to aqueous solutions to help determine possible product contaminants. Follow quality and documentation requirements for all laboratory work. Properly maintain required laboratory equipment. | 4/25/2022 |
| 6973 | NSF International/Amarex Germantown, MD Safety Associate BS in scientific or medical field Exp: 1+ years |
Responsibilities: Enter incoming safety events into related tracking systems and databases; Handle incoming safety-related reports from clinical trial sites; Process expedited/non-expedited safety events based on the Medical Monitor’s evaluation in accordance with company’s SOPs and other regulatory guidelines; Perform data reconciliation for ad hoc and annual safety reports | 4/26/2022 |
| 6974 | NSF International/Amarex Germantown, MD Programmer Analyst I BS in computer science or related Exp: 1 year |
Responsibilities: Identify, evaluate and solve clinical data collection problems; Develop and implement clinical data collection methods that meet FDA guidelines; Test, document, and validate clinical data collection computer systems; Develop user manuals; Demonstrate and train users on the application | 4/26/2022 |
| 6975 | AmbioPharm North Augusta, SC Purification Chemist I BS in Chemistry Exp: 0 years |
Responsibilities: Work in a cGMP environment to perform the peptide purification processes through chromatography as well as other various purification techniques; Use analytical skills to prevent and solve possible process complications and problems; Work as part of a team to complete specific projects in a timely manner; Follow approved cGMP manufacturing directions such as production batch records, standard operation procedures and standard test procedures; Help the team to install, test, operate and maintain equipment for manufacturing and in-process testing | 4/26/2022 |
| 6976 | AmbioPharm North Augusta, SC QC Chemist I BS in Chemistry or Life Science Exp: 1-2 years |
Responsibilities: Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments; Perform and review QC release testing; Support routine analytical testing using GC, KF, and HPLC; Assist the QC/QA group with writing and editing of SOPs and STPs | 4/26/2022 |
| 6977 | AmbioPharm North Augusta, SC QA Manufacturing Associate I (2nd Shift) BS in Chemistry or Life Science Exp: 1+ years |
Responsibilities: On the floor monitoring of facility / production manufacturing suites for compliance to SOPs, cGMP, cGDP, batch record review, and identify and resolve routine errors and prevent possible deviations affecting real-time production. This includes documentation completeness, HPLC integration review, managing calculation errors, deviations, and conformance to critical process parameters (CPP). Maintain a full understanding of all AmbioPharm SOPs and policies applicable to the manufacturing of APIs. | 4/26/2022 |
| 6978 | Ambry Genetics Aliso Viejo, CA Research Associate BS in Biology, Molecular Biology, Biochemistry or related Exp: 0-2 years |
Research Associate II is responsible for assisting senior R&D and Clinical Validation staffs with minimal supervision to design, develop, and validate clinical diagnostic assays spanning a wide range of Next-Generation sequencing and microarray technologies. | 4/26/2022 |
| 6979 | Ambry Genetics Aliso Viejo, CA Bioinformatics Associate MS in bioinformatics, computational biology, biophysics, biology and computer science, or related Exp: 0 years |
Responsibilities: Support clinical lab operation within Ambry in testing, running, troubleshooting, and maintaining bioinformatics pipelines and NGS projects with focus on TAT; Provide improvement for pipeline performances by collaboration with pipeline dev team to test new features for Ambry bioinformatics pipelines; Perform NGS data analysis and QA/QC platform; Write documentation and perform bioinformatics data analyses to support the Regulatory team with FDA submissions and requests. | 4/26/2022 |
| 6980 | Ambry Genetics Aliso Viejo, CA Lab Associate I (5pm-3:30am, Mon, Thurs-Sat) BS in science Exp: 0-2 years |
Responsibilities: Follow all procedures and protocols pertaining to patient sample processing, pre-analytical, analytical, and post-analytical testing and general laboratory system that do not directly involve the manipulation of patient samples or products generated from patient samples; Adhere to all Quality regulations (CAP, CLIA & New York State) and ensure all training and competency forms are complete; Perform biological specimen patient preparation, labeling, handling, preservation or fixation, processing or preparation, and transportation and storage of specimens. | 4/26/2022 |
| 6981 | Ambry Genetics Aliso Viejo, CA Lab Associate I (8am-4:30pm, Sun-Thurs) BS in science Exp: 0-2 years |
Responsibilities: Follow all procedures and protocols pertaining to patient sample processing, pre-analytical, analytical, and post-analytical testing and general laboratory system that do not directly involve the manipulation of patient samples or products generated from patient samples; Adhere to all Quality regulations (CAP, CLIA & New York State) and ensure all training and competency forms are complete; Perform biological specimen patient preparation, labeling, handling, preservation or fixation, processing or preparation, and transportation and storage of specimens. | 4/26/2022 |
| 6982 | Amide Technologies Cambridge, MA Research Associate/Technician - Peptide Chemistry BS or MS in in chemistry, chemical engineering, biochemistry, or related Exp: 0+ years |
In this role you will: Use proprietary flow chemistry synthesis technology to synthesize next-gen peptides/proteins; Use LCMS, Flash, HPLC and FPLC instrumentation to purify/analyze peptides and proteins; Use biophysical and functional techniques like DSF, CD, and BLI to validate protein fold/activity | 4/26/2022 |
| 6983 | Amneal Pharmaceuticals Brookhaven, NY Scientist I, Quality Control BA or BS in Chemistry or related Exp: 0+ years (1+ preferred) |
The Scientist I - QC is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 4/27/2022 |
| 6984 | Amneal Pharmaceuticals Branchburg Township, NJ Scientist I, Quality Control BA or BS in Chemistry or related Exp: 0+ years (1+ preferred) |
The Scientist I - QC is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 4/27/2022 |
| 6985 | Amneal Pharmaceuticals Piscataway, NJ Scientist I BS in Pharmacy or Chemistry Exp: 0+ years |
Activities include: Following schedules, direction of compendia standards and in-house standard operating procedures to analyze pharmaceutical drug substance, excipients, drug product testing for release and stability samples. Perform quantitative analysis for pharmaceutical drug-substances, excipients and drug products using USP/NF, EP, in-house test methods and standard protocols, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs. | 4/27/2022 |
| 6986 | Amneal Pharmaceuticals Bridgewater, NJ Scientist I, AR&D BA or BS in Chemistry or related Exp: 1+ years |
The Scientist-I position is an entry level, and it contributes to tasks associated to pharmaceutical analysis intended for drug product development. The preliminary activities include following schedules, direction of compendia standards and in-house standard operating procedures to analyze pharmaceutical drug substance, excipients, drug product testing for release and stability samples. | 4/27/2022 |
| 6987 | AnaSpec Fremont, CA Research Associate-Assay Kits BS in Biochemistry, Chemistry, Cell Biology or related Exp: 0-3 years |
Perform assay kit production and QC tests: enzyme activity assays, protein labelling and conjugation, protein expression/purification. Manage routine activities, including meticulous record keeping. Order laboratory supplies and reagents, maintain inventory. Participation in R&D projects expected. | 4/27/2022 |
| 6988 | AnaSpec Fremont, CA Research Associate-Antibodies BS in Biochemistry, Chemistry, Cell Biology or related Exp: 0-3 years |
Perform antibody purification and characterization, protein expression/purification; protein/peptide labeling and conjugation. Manage routine activities, including meticulous record keeping. Order laboratory supplies and reagents, maintain inventory. Participation in R&D projects expected. | 4/27/2022 |
| 6989 | AnaSpec Fremont, CA Synthesis Chemist I BS or MS in Chemistry, Organic Chemistry, or related Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). General Responsibilities: Perform the synthesis of peptides according to production procedures; Perform mass and purity analysis of in-process peptides using Matrix Assisted Laser Desorption- Time of Flight and High-Performance Liquid Chromatography; Complete and maintain written manufacturing documents | 4/27/2022 |
| 6990 | AnaSpec Fremont, CA QC Chemist BS in Chemistry or related Exp: 1+ years |
This position is responsible for performing analytical testing for various product lines, such as peptides, dyes, and unusual amino acids and ensures that the products are evaluated in a timely manner and meet all procedural requirements. | 4/27/2022 |
| 6991 | Anika Sarasota, FL Quality Engineer I BS in Mechanical Engineering, Biomedical Engineering, or related Exp: 0+ years |
Responsibilities: Work cross-functionally to evaluate product design features and product functionality; Analyze, trend, and summarize test and inspection data to identify product improvement; Evaluate product design features to determine appropriate tolerances, manufacturing requirements, measurement methods and acceptance criteria; Investigate product failures, nonconformities and complaints utilizing data for product improvement. | 4/27/2022 |
| 6992 | Ani Pharmaceuticals Baudette, MN Analytical Development Analyst BS or MS in Chemistry, Pharmacy, or related Exp: 1+ years |
Perform testing on material and product samples. Prepare standards, solutions, and samples in accordance with approved procedures. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate and report results in accordance with governing test methods and SOPs. Work with Supervisors to report discrepancies. | 4/28/2022 |
| 6993 | Ani Pharmaceuticals Baudette, MN QC Chemist BS in chemistry, biochemistry, microbiology, or related Exp: 1-5 years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 4/28/2022 |
| 6994 | Ansh Labs Webster, TX Product Manager BS in biological sciences or business Exp: 1-2 years |
The Product Manager will support design, development and distribution of all integrated marketing content and communications activities for the Ansh Labs biomedical reagents and immunodiagnostic product lines. Select activities may include distribution of global sales collateral, documenting customer feedback for technical support, direct marketing, digital marketing, website management, advertising, trade shows, and customer events. | 4/28/2022 |
| 6995 | Antibodies Incorporated Davis, CA Product Manager- Antibody Reagents MS in Life Sciences Exp: 1-3 years |
You will oversee continued production and quality control of our current antibody product catalog and also lead antibody development efforts to create new antibody products for our catalog. These new products will serve customer needs in the areas of neuroscience and cell biology research and be developed across a variety of antibody development platforms. The ideal candidate will have strong experience in mammalian cell culture, molecular biology, and with antibody-based assays | 4/28/2022 |
| 6996 | Antibody Solutions Santa Clara, CA Research Associate: Immunochemistry BS in Cell Biology, Molecular Biology, Microbiology, Biochemistry, or related Exp: 0-2 years |
The successful candidate will work with a team dedicated to the analysis of polyclonal sera and monoclonal antibodies for antibody discovery. Responsibilities include antigen and buffer formulation, designing and performing ELISA, Flow Cytometry, Biolayer Interferometry, and ELISpot assays, and data compilation and analysis. | 4/28/2022 |
| 6997 | Antibody Solutions Santa Clara, CA Research Associate: Cell Biology BS in Cell Biology, Molecular Biology, Microbiology, Biochemistry, or related Exp: 0-2 years |
The successful candidate will work with a team dedicated to the cellular aspects of antibody discovery. Responsibilities include isolation and immortalization of B-cells, cloning by FACS-sorting, cryopreservation & cell banking, and antibody production using bioreactors. | 4/28/2022 |
| 6998 | Applied Medical Rancho Santa Margarita, CA Process Engineer I BS in Mechanical, Biomedical, Industrial, or Manufacturing Engineering, or related Exp: 0+ years |
Responsibilities: Sustain manufacturing processes; Debug manufacturing processes and equipment via root cause analysis; Run, observe and expedite shop orders; Develop and update engineering documents such as process maps, process FMEA, manufacturing/quality Instructions, test methods, drawings, and test reports; Collaborate with the Production team to identify capabilities and capacity | 4/28/2022 |
| 6999 | Applied Medical Rancho Santa Margarita, CA Engineer I BS in engineering or science Exp: 0+ years |
Responsibilities: Conduct experiments to prove hypotheses; Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques; Implement statistical techniques to determine sample sizes and levels of confidence; Implement statistical process controls to monitor validated processes; Design engineering test protocols and use a data-driven approach to collect, analyze and summarize data into engineering reports | 4/28/2022 |
| 7000 | Applied Medical Rancho Santa Margarita, CA Electrical Engineer I BS in Electrical Engineering, Computer Engineering, or related Exp: 0-3 years |
Responsibilities: Schematic design of new and innovative projects; Analyze the hardware and firmware of embedded medical electrical systems with an emphasis on power management, digital and analog controls, and low frequency (500 kHz) high power (500 W) RF amplification; Participate in firmware creation for programmable logic devices such as DSPs, FPGAs, and CPLDs; Participate in hardware and firmware design reviews | 4/28/2022 |
| 7001 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I BS in engineering or science Exp: 0+ years |
Responsibilities: Conduct experiments to prove hypotheses; Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques; Implement statistical techniques to determine sample sizes and levels of confidence; Implement statistical process controls to monitor validated processes | 4/28/2022 |
| 7002 | Applied Medical Rancho Santa Margarita, CA Engineer I (Process/Electrical/Industrial) BS in Electrical, Biomedical, Industrial, System or Manufacturing Engineering, or related Exp: 0+ years |
As an Engineer I you will be responsible to provide engineering support to medical device development projects from design through production phase. Responsibilities include: Understand and follow Applied Medical's Quality Systems (QS); Design, investigate, develop and qualify new manufacturing processes, fixtures and equipment | 4/28/2022 |
| 7003 | Lonza Portsmouth , NH QC Deviation/Investigation Writer AA degree Exp: 1 yr |
User account support; Software application administration; Analytical instrument and computer systems commissioning and decommissioning; Perform other duties as assigned; Completes QC analytical instrument and software validation deliverables, writes GMP procedures, validation documents and executes test scripts; Software administration responsibilities include conversion of test methods, batch records and other written source documents into instrument computer system software. | 4/21/2022 |
| 7004 | Lonza Portsmouth , NH QC Systems Specialist BS Microbiology, Biology, similar Exp: 0 yrs |
Technical writing for the educated but uninformed reader, translate simple to moderate scientific events into a brief and cohesive report as a finished product. Accurately capture immediate actions and containment of the event, address comments from both internal and external clients on the compiled final report; Perform thorough investigations of Quality Control non-conforming events that could include review of cGMP documents and historical review of the quality management system; Perform investigations using structured root cause analysis tools (fishbone, 5 Why’s, etc.) and partner with team members to determine “true” root cause; Participate in defining “right” CAPA after investigation process is complete | 4/21/2022 |
| 7005 | Abveris Quincy, MA Research Associate - Tissue Culture BS in science Exp: 1+ years |
We are currently seeking a Research Associate for our cell culture group to support hybridoma and recombinant expression antibody discovery platforms. In this lab-based role, attention to detail, ability to multitask and working both independently and in group settings will be critical for success. You will work directly with the cell culture group for a range of projects to produce, select and scale hybridoma cell lines, while also supporting recombinant expression platforms in a rapidly growing environment that is always eager to optimize processes. | 4/19/2022 |
| 7006 | Accent Therapeutics Lexington, MA Research Associate/Senior Research Associate, Biology BS or MS in Biology Exp: 1-2 years |
Responsibilities: Execute cell and molecular biology studies to investigate the role of novel epitranscriptomic pathways in human disease; Assist with the development of cell-based assays to be used in support of medicinal chemistry efforts and structure activity relationship assessment; Maintain good written records of laboratory procedures, results and conclusions. | 4/19/2022 |
| 7007 | Aclaris Therapeutics Wayne, PA Clinical Trial Associate BS or BA in science Exp: 1-2 years |
Responsibilities: Collecting, registering, and archiving information and documents in accordance with the applicable GCP guidelines for clinical studies and corresponding Aclaris Standard Operating Procedures; Maintenance of Trial Master File (TMF) and Investigator Site Files (ISF) to ensure regulatory compliance and audit readiness; Collection and tracking of regulatory documents for study start-up and IRB submissions; provide oversight of Contract Research Organization (CRO) managed studies to ensure these activities are completed | 4/19/2022 |
| 7008 | Acro Biosystems Newark, DE Lab Technician BS or MS in Biology, Microbiology, Cell Biology, Molecular Biology, Immunology, Biochemistry, or related Exp: 1+ years |
Responsibilities: Adhere to established procedures and methodologies, e.g. ELISA, , Western blot, SPR and cell-based assays; Record critical data and test results, perform data analysis as directed; Assist supervisor in planning research protocols and procedures and summarizing analysis data; Support supervisor, project leaders, and other professional staff with information exchange and clarification | 4/19/2022 |
| 7009 | Acro Biosystems Various, WA Sales Representative BS in Biological or Biomedical Sciences Exp: 0-2 years |
We are looking for a Sales Representative to support commercial activities in the Washington territory. In this position, you will be responsible for maintaining existing customers and pursuing new customers, as well as increasing customer base in the territory. You will also be extensively involved in building customer relationships and providing all-around support to our customers. Travel within the territory 40-50% of the time. | 4/19/2022 |
| 7010 | Acumed Hillsboro, OR Process Validation Engineer I BS in engineering or science Exp: 1-3 years |
The Process Validation Engineer (PVE) tests systems and processes as the owner of the process validation program to ensure the highest quality products are manufactured. S/he investigates process deviations, investigates assignable root causes for equipment, system or process failures and establishes appropriate corrective and preventive actions. | 4/19/2022 |
| 7011 | Supernus Rockville, MD Clinical Research Associate I BS in science or nursing Exp: 0+ years |
Responsibilities: Assists with the development and/or review of study-related materials including CRFs, protocols, informed consent forms, monitoring plan, etc.; Participates in the identification and recruitment of investigators; Assists in the development of subject recruitment strategies and materials; Ensures adequate reporting/tracking of adverse events, protocol deviations and subject status; Serves as a contact for study site personnel to answer questions and resolve study-related issues. | 4/19/2022 |
| 7012 | Supernus Rockville, MD Chemist BS in Chemistry or related Exp: 0+ years |
To provide QC support for solid dosage forms, primarily by using dissolution testing, spectroscopy, HPLC, wet chemistry, maintaining logbooks and performing data management/report writing as necessary. | 4/19/2022 |
| 7013 | Adimab Lebanon, NH Lab Assistant BS in science Exp: 0+ years |
We are seeking an organized and dependable Laboratory Assistant to join our Operations Team. The Laboratory Assistant will primarily provide support to the lab management team. The successful candidate will possess the strong business judgment and communication skills needed to interact with a variety of people and job functions. | 4/19/2022 |
| 7014 | Adimab Lebanon, NH Research Associate - Antibody Engineering BS in molecular biology, chemical engineering, biochemistry, or related Exp: 1+ years |
Responsibilities: Yeast propagation and handling; Construct antibody libraries and perform selections; Discover antibodies using flow cytometry and/or mammalian cell panning; Contribute to technology development aimed at improving our core technology; Collect, organize, and analyze antibody characterization data; Successfully collaborate with colleagues | 4/19/2022 |
| 7015 | Adimab Lebanon, NH Research Associate - Antibody Sciences BS in molecular biology, bioengineering, chemical engineering, or biochemistry Exp: 1+ years |
Responsibilities: Camelid lymphocyte sample handling and characterization; Primary B cell analysis using flow cytometry; Design of immunization schemes for in vivo antibody discovery campaigns; Serological analyses using numerous methods including ELISA and cell binding by flow cytometry | 4/19/2022 |
| 7016 | Adimab Lebanon, NH Research Associate - HTE Yeast Team BS in biology, molecular biology, chemical engineering, biochemistry, or related Exp: 1+ years |
Responsibilities: Production group media prep; Production platform routine plate handling; Downstream delivery handling; Filling in with our dish, media and inventory roles when needed; Provide high quality work in a dynamic, fast-paced environment | 4/19/2022 |
| 7017 | Adma Biologics Boca Raton, FL QC Microbiologist I BS in Biological Sciences or related Exp: 0-3 years |
Perform microbiological and chemical testing for product, in-process samples, and raw materials according to approved Standard Operating Procedures (SOP’s). This testing including, but is not limited to, Bioburden, Microbials, Bacterial Endotoxin Testing, Microbial Identifications, TOC/Conductivity, Sterility Testing, Growth Promotion and Enumeration of Biological Indicators. | 4/19/2022 |
| 7018 | Adma Biologics Boca Raton, FL Technician I, Manufacturing Purification BS in Chemistry or Life Science Exp: 0 years |
This position is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. | 4/19/2022 |
| 7019 | Adma Biologics Boca Raton, FL Chemist I BS in Chemistry, Biochemistry, Molecular Biology, or related Exp: 0-3 years |
The Chemist I will Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. | 4/19/2022 |
| 7020 | Adma Biologics Boca Raton, FL Microbiologist I QC, Environmental Monitoring BS in Biological Sciences or related Exp: 0-3 years |
The Microbiologist I Environmental Monitoring will perform environmental monitoring and water sampling within the controlled manufacturing areas and QC Laboratory | 4/19/2022 |
| 7021 | Adma Biologics Boca Raton, FL QC Lab Support Associate I BS in Biology, Chemistry, Medical Technology, or related Exp: 1-3 years |
Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with other QC projects. | 4/19/2022 |
| 7022 | Admera Health South Plainfield, NJ Associate Scientist I/II BS or MS in Biological Sciences Exp: 1-3 years |
Responsibilities: Preparing solutions and reagents for performing assays on the bench; Perform Next Generation Sequencing-based genomic assays on different workflows (ex. Genome Sequencing); Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance | 4/19/2022 |
| 7023 | Affini-T Therapeutics Watertown, MA Scientist, TCR Discovery BS or MS or PhD in Biological Sciences or related Exp: 1+ years |
Responsibilities: Design, execute and critically analyze in vitro experiments to develop and characterize TCR-engineered T cell therapy products; Able to independently manage their workload, design and perform bench activities independently or with minimal supervision; Able to manage project timelines and perform time sensitive experiments to drive discovery programs accordingly with departmental, functional and external stakeholders; Apply recent developments in cell therapy-related novel technologies to design and create the next generation cell therapy platforms. (Title commensurate with experience) | 4/19/2022 |
| 7024 | Ajinomoto Bio-Pharma Services San Diego, CA Manufacturing Quality Assurance Associate I (1st shift) BS in Life Sciences or related Exp: 0-2 years |
In this role, you will provide QA oversight and support during manufacturing operations. The Associate I performs documentation review and ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. The Associate I promotes a cGMP environment and collaborates with internal team members to ensure compliance to specifications, processes, and procedures. | 4/19/2022 |
| 7025 | Ajinomoto Bio-Pharma Services San Diego, CA Microbiology Technician BS in Life Sciences or related Exp: 0-2 years |
This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 4/19/2022 |
| 7026 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Associate I BS in science or engineering Exp: 0-2 years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 4/19/2022 |
| 7027 | Akoya Biosciences Menlo Park, CA Bioinformatician / Data Scientist I MS or PhD in Bioinformatics, Data Science, Computer Science, Computer Vision, Machine Learning, Statistics or Applied Mathematics Exp: 1+ years |
The Data Scientist will analyze datasets generated within our Spatial Tissue Exploration Program, a fee-based technology access services to academic, biotech and pharma clients. The goal of the analyses is to provide customers and collaborators with access to curated data from high quality Spatial Biology data generated on Akoya platforms. The Data Scientist will encounter diverse data and varied analytical & biological problems but will follow a common workflow logic. | 4/19/2022 |
| 7028 | Alcami Wilmington, NC Associate Scientist I BS in Pharmaceutical Sciences, Chemistry, or related Exp: 0+ years |
The Associate Scientist I is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist I may also assist with method development/method validation projects. Typical types of testing: assays (potencies, related substances, residual solvents, metals etc.), rate of release (dissolution), moisture content, identification, and various other wet chemistry based measurements, including HPLC and GC. | 4/20/2022 |
| 7029 | Alcami Charleston, SC Associate Scientist I, Microbiology (2nd Shift) BS in Chemistry, Biology, Microbiology or related Exp: 0-2 years |
The Associate Scientist I is accountable for driving results in a fast-paced environment. The position is responsible for performing monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The incumbent will provide support to manufacturing and laboratory operations. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 4/20/2022 |
| 7030 | Alcami Wilmington, NC Associate Scientist II MS in Pharmaceutical Sciences, Chemistry, or related Exp: 0+ years |
The Associate Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also assist with method development/method validation projects. Key methodologies applied include: HPLC, GC, titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). | 4/20/2022 |
| 7031 | Alkahest San Carlos, CA Research Associate - Proteomics BS or MS in Chemistry, Biology, Biochemistry, or related Exp: 1+ years |
We are seeking a highly motivated Research Associate who will help advance our preclinical scientific activities to identify and characterize proteins associated with aging and disease. The role will primarily support proteomic analysis by state-of-the-art technologies including mass spectrometry and immunoassays. Studies performed will involve cutting edge science and require innovative concepts and strategies. | 4/20/2022 |
| 7032 | Alliance Pharma Malvern, PA Analyst to Senior Scientist (multiple positions available) BS/MS/PhD in Biology, Molecular Biology, Immunology, Biotechnology or related Exp: 0-10+ years |
We currently have several positions ranging from Analyst to Sr. Scientist available to conduct bioanalytical analysis using ELISA /Immunoassay /Ligand Binding Assay/ qPCR methodology in Biopharmaceutical laboratory in Malvern, PA. Responsibilities include: Development, qualification or validation of ELISA / immunoassay in a variety of biological matrices; Sample Analysis using ELISA / Immunoassay/ qPCR assay / cell-based assay / Enzymatic Assay | 4/20/2022 |
| 7033 | Alliance Pharma Malvern, PA Laboratory Technician BS in Chemistry Exp: 0+ years |
Job Duties: Perform routine laboratory work entailing sample receiving, sample extraction and analysis using LC-MS/MS, or ELISA, data processing, report writing, instrument maintenance, in vitro metabolism work, and daily lab organization; Fully understand regulatory compliance, follow Good Laboratory Practice (GLP) guidance and our internal SOPs to conduct bioanalysis, cooperate with QA, management, colleagues and clients. | 4/20/2022 |
| 7034 | Allogene South San Francisco, CA Sr. Associate Scientist/Associate Scientist, Process Development BS or MS in Chemical Engineering, Biochemistry, Molecular & Cell Biology, Immunology Exp: BS: 0-7 years; MS: 0-4 years |
This individual will contribute to the development, implementation, and characterization of state-of-the-art processing technologies to deliver scalable and robust manufacturing processes and support successful tech transfer for GMP manufacturing and release at a CMO. This position will also contribute to the development of novel technologies and approaches to meet future CAR T manufacturing needs. | 4/20/2022 |
| 7035 | Allogene Newark, CA Analyst I, QC Sample Management (Contract) BS in science Exp: 1+ years |
You will lead and oversee sample management workflows and contribute to the broader state of the art facility for storage and distribution of biologic samples within internal and external CMOs/CTL partnering sites. You will also handle protein samples distribution, management, and process assessments and logistic improvements and act as the primary point of contact for biological sample logistics and deliverables. You will support logistical activities in the sample management office and stability labs. | 4/20/2022 |
| 7036 | Allogene South San Francisco, CA Scientist/ Sr. Associate Scientist, Cell Engineering MS in Molecular Biology, Cell Biology, Immunology, Genetics, Chemical Engineering, Biochemistry or related Exp: 1-5 years |
The candidate will perform experiments to develop, evaluate, and improve cell engineering technologies, using programmable nucleases and site-specific integration of transgenes using viral and non-viral delivery systems. Perform in vitro molecular and cell-based assays to evaluate cell engineering technologies required for the project and analyze the resulting data | 4/20/2022 |
| 7037 | Alltrna Cambridge, MA Research Associate/ Senior Research Associate – Cell Biology (Cell Engineering & Disease Modeling) BS or MS in Cellular or Molecular Biology, or related Exp: 0-5+ years |
Responsibilities: Maintain, culture and perform quality control testing of mammalian cells and primary cells; Engineering mammalian and pluripotent stem cells for disease reporter assays and disease modeling; Design and production of cell engineering tools such as DNA constructs, gRNAs (CRISPR), and lentiviruses, etc.; Develop, optimize, and execute robust cellular and biochemical assays to support hid-to-lead and lead optimization | 4/20/2022 |
| 7038 | Alnylam Cambridge, MA Associate Scientist II BS in Chemistry Exp: 1-3 years |
Responsibilities: Support oligonucleotide synthesis method development, optimization and scaling up; Support downstream processing method optimization; Execution of oligonucleotide synthesis and downstream processes to provide the research and in-house non-GMP material in a tight timeline; Execution of in-process analytical tests; Participate in creating and reviewing SOPs and batch records in support of the in-house non-GMP manufacture | 4/20/2022 |
| 7039 | Alnylam Cambridge, MA Associate Scientist II, In Vivo Sciences BS in Biology or related Exp: 1-3 years |
An Associate Scientist II is responsible for organizing, conducting, and reporting non-GLP rodent toxicology, investigative, and pharmacokinetics/toxicokinetics (PK/TK) studies that support drug discovery and development. | 4/20/2022 |
| 7040 | Alnylam Cambridge, MA Clinical Trial Associate BS/BA in science or healthcare related field Exp: 1+ years |
The Clinical Trial Associate is highly attentive to details, has strong organizational skills, and able to communicate effectively in a fast paced environment. Major responsibilities for this position include maintenance of informational databases and program tracking reports, participate in coordination of clinical trial related activities, authoring of study operations manuals, budgetary oversight and tracking, and providing general program support in a team setting to ensure the successful execution of clinical trial tasks and deliverables according to project timelines. | 4/20/2022 |
| 7041 | Alnylam Cambridge, MA Quality Control Analyst I BS in Analytical Chemistry, Biochemistry, Chemistry, Biology, or related Exp: 0-2 years |
The Quality Control Analyst I- Microbiology will be primarily responsible for performing routine environmental monitoring (EM), critical utility (CU) sampling, and testing of in-process and bulk drug product materials in support of our new GMP manufacturing at the Alnylam – Norton facility, 20 Commerce Way, Norton, MA and supporting the Alewife facility, 665 Concord Avenue, Cambridge, MA. Demonstrated technical ability in QC microbiology and understanding of microbiological methodology is required. | 4/20/2022 |
| 7042 | Alnylam Cambridge, MA Associate Scientist II, in Vivo Pharmacology BS or MS in Animal/Veterinary Sciences, Cell/Molecular Biology, Biochemistry, or related Exp: 0-3 years |
Responsibilities: The candidate will engage in investigative RNAi research evaluating siRNA delivery to diverse tissues in a variety of animal models; Develop and perform in vivo and ex vivo studies using molecular and biochemical techniques to characterize distribution and activity of conjugated siRNAs; Willing to learn new techniques to support in vivo studies; Responsible for data entry, data analysis in timely manner, and preparation of clearly articulated experimental reports. | 4/20/2022 |
| 7043 | Alnylam Cambridge, MA Associate Scientist II, RNAi Discovery BS in Cellular or Molecular Biology Exp: 1+ years |
Responsibilities: Perform cell culture (iPSCs, primary cells, immortalized cell lines) to support the research needs of the group; Support lab maintenance including reagent inventory and reagent preparation; The candidate will perform high-throughput screening of siRNAs using qPCR and a variety of cell-based assays; Design and execute in vitro screens and assays to characterize novel siRNA modifications that impact activity or uptake. | 4/20/2022 |
| 7044 | Alnylam Cambridge, MA Associate Scientist II, Bioanalytical Sciences MS in Biology, Chemistry, Biochemistry, or related Exp: 1+ years |
We are seeking a highly motivated Associate Scientist II to join our team to help advance novel RNAi therapeutic programs from discovery to the clinic. The Bioanalytical Associate Scientist will contribute to designing, developing and implementing biologically relevant assays to support early through late stage drug development programs using techniques such as ligand binding assays (ELISA, MSD, Luminex, Quanterix), cell based assays, or hybridization assays. They will execute assays and analyze results to evaluate PK/TK, metabolism, drug distribution, drug mechanism of action, PD, and biomarkers to advance RNAi therapeutic development. | 4/20/2022 |
| 7045 | Boston Analytical Salem, NH Quality Assurance Specialist Bachelor’s degree in a related science discipline Exp: 0-1 years |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing chemists analytical data, routine work, protocols and reports. | 4/18/2022 |
| 7046 | Boston Analytical Salem, NH Analytical Chemist Bachelor’s degree in Chemistry or a related science discipline Exp: 0-2 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 4/18/2022 |
| 7047 | Boston Analytical Salem, NH Microbiologist – QC BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. The schedule for this position is Monday through Thursday from 1:00pm-11:30pm. | 4/18/2022 |
| 7048 | Boston Analytical Salem, NH Microbiologist – Microbiome BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. The schedule for this position is Monday through Thursday working 1:00pm-11:30pm. | 4/18/2022 |
| 7049 | Boston Analytical Morrisville, NC Microbiologist – Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. This position is located in Morrisville, North Carolina. | 4/18/2022 |
| 7050 | Boston Institute of Biotechnology Southborough, MA Research Associate / Scientist / Sr. Scientist – Downstream Process Development MS degree in Biochemistry or Chemical Engineering Exp: 0-5 years |
Essential requirements for this position include in-depth understanding and hands-on experience with recombinant protein purification from different expression hosts (including E. coli, Yeast, CHO and HEK) and an aptitude for careful, detail-oriented experimentation. The level of the position will be commensurate with the candidate’s experiences. | 4/18/2022 |
| 7051 | BostonGene Waltham, MA Research Associate, Molecular Biology and Next Generation Sequencing Bachelor’s (B.S.) degree in biology, clinical laboratory science, medical technology or related discipline Exp: 0-2 years |
BostonGene is seeking a highly motivated Junior Research Associate to join our R&D team in our laboratory located in Waltham, MA. This candidate will support BostonGene’s state-of-the-art primary next generation sequencing (NGS), adjunct analytical platforms, and automated analysis pipelines. The candidate will be expected to develop proficiencies in NGS support protocols, such as RNA and DNA isolation from tissue, cell free DNA isolation from plasma, Whole Exome Sequencing library preparation, RNA-Seq library preparation, qPCR, Molecular Biology techniques, and other sample QC techniques. | 4/18/2022 |
| 7052 | Boundless Bio La Jolla, CA Research Associate/Senior Research Associate, Drug Discovery BS/MS in biology related field Exp: 1-3 years |
As a Research Associate/Senior Research Associate at Boundless Bio, you will play a significant role in helping us transform exciting extrachromosomal DNA (ecDNA) discoveries into cancer medicines of the future. You will contribute to the process of developing robust, miniaturized high-throughput assays designed to enable drug discovery programs supporting multiple ecDNA-directed targets. This will involve broad application of biochemical and cellular assays across a range of formats to enable screening and SAR campaigns in support of our drug pipeline. These efforts will make an important contribution to the Boundless Bio drive for innovation in targeting difficult to treat cancers. | 4/18/2022 |
| 7053 | BPS Bioscience San Diego, CA Research Associate, Biochemical Assay and Assay Development Bachelor's Degree in Biochemistry, Molecular Biology, Cell Biology, Biophysics, or a related field is required. Exp: Entry-level |
BPS Bioscience is seeking a Reseach Associate in our Biochemical Assay Development department. Functioning somewhat independently, this person will assist with and conduct laboratory experiments on research projects within well-defined guidelines; will be responsible for the enzyme assay optimization, perform quality control experiments on new protein purifications, and the compound testing in the biochemical assay following the protocol under the supervision of Sr. Scientists. | 4/18/2022 |
| 7054 | BPS Bioscience San Diego, CA Research Associate, Cell Biology BS or MS in Virology, Cell Biology, or relevant scientific discipline. Exp: Entry-level |
BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, lentivirus, and recombinant cell lines for drug discovery. We are seeking a highly motivated individual with experience in lentivirus production or immunotherapy to join our dynamic team as a Research Associate / Senior Research Associate. | 4/18/2022 |
| 7055 | BPS Bioscience San Diego, CA Research Associate, Cell Line and Assay Development Bachelor's or Master’s Degree in Biology is required. Exp: Entry-level |
The position requires the ability to perform and independently interpret molecular cloning and mammalian cell culture experiments. The successful candidate will be responsible for routine tissue culture in mammalian cells (including induced pluripotent stem cells) involving techniques such as transient transfections and establishment of stable cell lines, and cell based assays. The candidate must be able to work independently and perform experiments to a very high standard, troubleshoot technical and scientific problems and effectively progress multiple projects simultaneously. | 4/18/2022 |
| 7056 | Abcam Branford, CT Research Associate B.S. degree in biology, immunology or related discipline Exp: 0-3 years |
We are seeking a Senior Research Associate/Research Associate to work on the Assay Team in the Partnerships and Custom Antibodies Team. A successful candidate will work as part of a team to deliver best-in-class antibodies and reagents to Abcam's customers and partners. This role reports to the Senior Scientist for Assay Development. The ideal candidate will have experience in ELISA, Western Blotting, ICC and Flow Cytometry. The environment is fun and fast-paced, with everybody working together as team to deliver the best products to our customers in a timely manner. | 4/21/2022 |
| 7057 | AstraZeneca Gaithersburg, MD Associate Scientist, Purification Process Sciences BS/BA or MS/MA biology, biochemistry, chemical/biochemical engineering, or related field Exp: 0+ years |
The position resides in the Purification Process Sciences group (PPS) within the Bioprocess Development R&D (BPD) department. The main responsibility will be the development of purification processes for biologics. Members of the PPS function work closely with other development functions and manufacturing sciences to develop and transfer clinical and commercial purification processes. | 4/21/2022 |
| 7058 | AstraZeneca Gaithersburg, MD Associate Scientist / Scientist - Analytical Quality/Chromatography AS: bachelor’s or master’s degree or equivalent in biology, chemistry, or related field. Exp: AS-BS: 1+ years; or MS |
The successful candidate will be responsible for working collaboratively in the Analytical Sciences GMP laboratory team, to ensure that release and stability testing of clinical trial material is performed according to international regulatory and AstraZeneca requirements. | 4/21/2022 |
| 7059 | AstraZeneca Gaithersburg, MD Associate Scientist / Scientist - Analytical Quality/Electrophoresis AS: bachelor’s or master’s degree or equivalent in biology, chemistry, or related field. Exp: AS-BS: 1+ years; or MS |
The successful candidate will be responsible for working collaboratively in the Analytical Sciences GMP laboratory team, to ensure that release and stability testing of clinical trial material is performed according to international regulatory and AstraZeneca requirements. | 4/21/2022 |
| 7060 | AstraZeneca Gaithersburg, MD Associate Scientist / Scientist BS/MS in Chemical/Biochemical Engineering, Biotechnology, Biochemistry, or Biological Sciences Exp: AS: 0+ years |
This position within Cell Culture and Fermentation Sciences will involve substantial amount of hands on cell culture work to develop, scale up, and characterize mammalian culture processes. The candidate with relevant prior experience will be preferred. This person will be expected to execute experiments on a routine basis to develop and characterize the upstream cell culture processes and be familiar with the basics of DOE including screening and optimization designs. Additionally, you are expected to be well familiar with the basics of bioreactor characterization (liquid liquid mixing and gas liquid mass transfer) and harvest development (TFF, centrifugation and depth filtration). This person must also know various methodologies that are typically used for scale up and scale down of cell culture and harvest processes. Finally, you are expected to possess strong mathematical skills for data analysis and process modeling. Must maintain clean orderly work environment to guarantee the success of aseptic operations. The candidate is also expected to maintain accurate and updated laboratory notebooks and to author technical reports and make relevant presentations in the department and project team meetings. Responsible for ordering chemicals and miscellaneous lab items and keeping track of the key inventory items for ongoing projects. | 4/21/2022 |
| 7061 | AstraZeneca Gaithersburg, MD Associate Scientist / Scientist, Cell Culture & Fermentation Sciences Bachelor’s or master’s degree in chemical/biochemical engineering, biotechnology, biochemistry, or biological sciences. Exp: AS: 0+ years |
This position within Cell Culture and Fermentation Sciences will involve a substantial amount of hands on cell culture work to develop, scale up, and characterize mammalian culture processes. | 4/21/2022 |
| 7062 | AstraZeneca Gaithersburg, MD Associate Scientist, Physiochemical Development Bachelor's or Master's degree or equivalent in Biology, Chemistry or Biochemistry Exp: 0+ years |
In this role you will carry out analytical testing using Chromatography, Electrophoresis, and/or Mass Spectrometry techniques in supporting development, manufacturing, and characterization of biopharmaceutical products, such as humanized monoclonal antibodies, antibody-drug conjugates, and recombinant proteins. The Associate Scientist will make detailed experimental observations, review and analyze data, might need to interpret experimental results, summarize data for presentations and reports. This role will have opportunity to author/revise SOPs, protocols, reports and other relevant documentation. | 4/21/2022 |
| 7063 | Bachem Torrance, CA Analytical Scientist Master’s Degree in analytical chemistry or related scientific field Exp: 1 year |
The Analytical Scientist will fulfill a critical role in GMP operations. This individual helps with the execution of feasibility evaluation of analytical methods, method development and validations, writing of validation protocols, reports and other technical quality documents; conducts validation related investigations and contributes to improvements in laboratory operations. | 4/21/2022 |
| 7064 | Bachem Vista, CA Production Chemist BS degree in Chemistry or related field Exp: 1-5 years’ |
The Chemist function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. | 4/21/2022 |
| 7065 | Aurora Biolabs San Diego, CA Research Associate I Bachelor's Degree in science related field Exp: 0-1 year |
The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. | 4/13/2022 |
| 7066 | Avedro [Glaukos] Burlington, MA Research Scientist Masters or Bachelors degree in analytical/formulation chemistry or biochemistry. Exp: 1-3 years |
This highly motivated Research Scientist will work within a small multidisciplinary project team, supporting focused research efforts into novel therapies to treat the eye. This individual will be responsible for conducting laboratory-based research, including formulation development, implementation and execution of biochemical assays and analytical protocols. Accurate and timely presentation and recording of data in lab notebooks and electronic files will be a priority. | 4/13/2022 |
| 7067 | Avid Bioservices Tustin, CA Research Associate/Sr. Research Associate, Downstream (Purification) Process Development Master's degree Exp: 1 to 2 years |
The Research Associate provides laboratory support for Process Development and performs a range of activities (while the Sr. position performs at a senior level). The employee may be assigned various tasks within the department to complete. | 4/13/2022 |
| 7068 | Avitide Lebanon, NH Manufacturing Technician Bachelor degree in Biotechnology or Biology (or related field) Exp: 1-2 years’ |
This qualified candidate will manufacture Avitide-Repligen biopharmaceutical affinity chromatography products in accordance with established manufacturing practices and procedures in compliance with quality regulations and guidelines. | 4/13/2022 |
| 7069 | Beam Therapeutics Cambridge, MA Research Associate/Sr. Research Associate, Analytical Sciences (Science Management) MS in Biochemistry, Chemistry, Biotechnology, Biosciences Management or related disciplines. Exp: 1+ year |
Do you have exceptional organizational skills, a science background, and a desire to step out of the lab and pursue a new carrier as a scientific manager? The Analytical Sciences team at Beam Therapeutic is seeking an individual with a biology, chemistry or biotechnology background and a passion for Project Management practices and collaboration tools such as Sharepoint, Smartsheet, and more. You will contribute to the coordination of lab activities and meetinigs of a multidisciplinary team, working with Beam teams and external partners. | 4/13/2022 |
| 7070 | Beam Therapeutics Cambridge, MA Research Associate BA/BS Exp: 1 year |
Beam is currently seeking a self-motivated and technically competent research associate to join our team. They will support our exploratory research by participating in the day-to-day operations of animal husbandry and care activities. The candidate will be responsible for maintenance of holding and procedure spaces, associated documents and records regarding training, procurement, and animal health monitoring. | 4/13/2022 |
| 7071 | Beam Therapeutics Cambridge, MA Research Associate, In Vivo Therapeutics Delivery BA/BS or MS Exp: 1-2 years’ |
Beam is seeking a self-motivated and technically competent research associate to join our team. They will support our exploratory research in disease target validation using gene editing tools in various different organs. The candidate will be responsible for conducting preclinical animal studies to support the development of therapies. They will also perform downstream RNA/DNA extractions and histological analyses. | 4/13/2022 |
| 7072 | Beam Therapeutics Cambridge, MA Research Associate, Next Generation Sequencing Core BA/BS in molecular biology, biotechnology, biochemistry, or other relevant scientific degree. Exp: 1-3+ years’ |
Beam Therapeutics is seeking a Research Associate to execute high throughput sample processing within the next generation sequencing (NGS) core. This position requires technical knowledge in NGS instrumentation and sample processing in addition to high throughput molecular biology experience. This position will work closely with other core R&D functions at Beam, including laboratory automation, LIMS, and bioinformatics, to provide researchers with a world class R&D platform. | 4/13/2022 |
| 7073 | Beam Therapeutics Cambridge, MA Process Sciences Engineer BS/MS degree Exp: 0-5 years |
Beam Therapeutics is seeking an energetic, talented Process Sciences Engineer with familiarity of nanoparticle formulation and process development. Reporting to the Director of Process Sciences the candidate will work as part of a team to scale up and optimize lipid nanoparticles (LNPs) for delivery of base editors. They will work as part of a team to develop and scale a manufacturing process with the ultimate goal of bringing in vivo base editing to patients. The ideal candidate should have good understanding of process optimization and nanoparticle formulation. We are looking for an ambitious candidate who wants to grow within in the process development group. | 4/13/2022 |
| 7074 | Beam Therapeutics RTP, NC Analyst, Quality Control Microbiology Bachelors in a scientific discipline. Exp: 1-2 years |
The Quality Control Microbiology Analyst will support the implementation of core Microbiology programs at Beam’s manufacturing facility in RTP, North Carolina. The NC manufacturing facility is a greenfield build and will be implemented in phases over a 6-8 Year period, with a focus on advanced therapeutic manufacturing technologies (cell and gene therapy modalities). The facility will start as a clinical phase manufacturing plant with the intent to move programs to commercial within the same facility. The incumbent will execute technical tasks and duties in support of the facility startup plan. These duties include environmental monitoring, Gram stain, media growth promotion, endotoxin, bioburden, and rapid sterility. The QC Microbiology Analyst works with colleagues in other Quality Control teams, as well as colleagues in QA, Manufacturing, and Validation to ensure that Microbiology programs are executed as per established requirements. The work schedule will provide support for site implementation activities and establishment of routine operations. | 4/13/2022 |
| 7075 | Berkshire Sterile Manufacturing Lee, MA Process Engineering Associate Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science Exp: one (1) year |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 4/13/2022 |
| 7076 | Biocare Medical Pacheco, CA Associate I, Protein Chemistry Bachelor’s degree in a scientific field Exp: one plus (1+) years’ |
The Protein Chemistry Associate I will take an active role in material processing, reagent formulation, technical manufacturing, and in-process and/or final quality control of reagents for use as components of in-vitro diagnostic (IVD) products. Specifically, he/she is involved in bioconjugation, protein purification, and analytical characterization of complex bioconjugates as they relate to the development of tissue diagnostic products for cancer and infectious disease. This position requires the person to adhere to all current industry standard regulations. | 4/13/2022 |
| 7077 | Biomere Richmond, CA Research Associate (Small & Large Animal) AS or BS Degree in Science (or equivalent degree) preferred. Exp: Research Associate I: 1 or 2 years |
Research Associate works under the direct guidance of the Site Head and the general guidance of the senior staff. Research Associate is proficient in animal procedures/animal husbandry, grant, internal, and/or contract research studies according to the study protocols and to the company guidelines and standard operating procedures (SOPs). | 4/13/2022 |
| 7078 | BioNano Genomics San Diego, CA Research Associate II, NPI MS degree in Molecular Biology, Biochemistry or Bioengineering. Exp: 1+ years |
Bionano Genomics is seeking a Research Associate II to conduct Reagent Process Development studies within the Assay and Reagents Team. In this position, the person will execute experiments to characterize both new and on-market products and will assist with developing manufacturing processes for new products. The candidate should have previous hands-on laboratory experience, including reagent formulations, sample generation, analytical assay and preferably genomics assay development experience. Previous experience in Manufacturing or Quality Control is beneficial, but not required. | 4/13/2022 |
| 7079 | BlueRock Therapeutics New York City, NY Research Associate I/II, Discovery Analytics Bachelors in biological sciences Exp: 0-2 years |
As part of BlueRock Therapeutics vision to change the future of medicine by enabling ground-breaking cell therapies, the candidate will be a key technical contributor of a dynamic and progressive team pioneering scaled somatic cell manufacturing processes utilizing state-of-the art culturing technology at increasing scales. The successful candidate will drive assay discovery and development at BlueRock, NY, establishing critical characterization and quality assays for cell therapy products and manufacturing processes with some supervision. Expertise in cell and molecular biology is required. The ideal candidate will be a highly motivated individual who leads from the bench and enjoys having broad responsibilities and opportunities. Collaboration with a highly driven, world-class team of scientists and engineers promises an exciting and engaging work environment for motivated, self-starting candidates. | 4/14/2022 |
| 7080 | BlueRock Therapeutics New York City, NY Research Associate(s) I/II, Stem Cell Genome Engineering B.Sc. or M.Sc. in cell biology, molecular biology, genetics, or related discipline Exp: up to 5 years |
Our cell line engineering team at the New York site is seeking a Research Associate I/II with a background in molecular and cell biology. The candidate will be a technical contributor in a dynamic and progressive team pioneering the generation of genome-modified therapeutic cells from human pluripotent stem cells (hPSCs). Together with other team members and direction from the lead scientist, the individual will contribute to the design and execution of a variety of genetic modifications that enhance cellular properties. This will include the use of gene editing technologies such as CRISPR/Cas-mediated homologous recombination to establish cell lines for BlueRock’s research pipeline that are altered in their genome to provide novel morphology or function. | 4/14/2022 |
| 7081 | BlueRock Therapeutics Cambridge, MA Research Associate(s) I/II, Stem Cell Genome Engineering B.Sc. or M.Sc. in cell biology, molecular biology, genetics, or related discipline Exp: up to 5 years |
Our cell line engineering team at the Cambridge, MA site is seeking a Research Associate I/II with a background in molecular and cell biology. The candidate will be a technical contributor in a dynamic and progressive team pioneering the generation of genome-modified therapeutic cells from human pluripotent stem cells (hPSCs). Together with other team members and direction from the lead scientist, the individual will contribute to the design and execution of a variety of genetic modifications that enhance cellular properties. This will include the use of gene editing technologies such as CRISPR/Cas-mediated homologous recombination to establish cell lines for BlueRock’s research pipeline that are altered in their genome to provide novel morphology or function. | 4/14/2022 |
| 7082 | Visby Medical San Jose, CA Lab Assistant / Device Tester Bachelor’s Degree, preferably in a scientific field. Exp: Entry level |
We are now looking to hire a Lab Assistant / Device Tester for a temporary position on its assay development team. The Lab Assistant/ Device Tester will execute a variety of tasks in support of the development team. This position reports to the Director, Assay Integration. | 4/14/2022 |
| 7083 | Visby Medical San Jose, CA Clinical Research Assistant Bachelor’s Degree, preferably in a life science or health science discipline. Exp: 1-2 years |
The Clinical Research Assistant is primarily responsible for the coordination of activities associated with the support of setup and management of clinical studies under the direction of, or as delegated by a member of the Clinical Trial team. | 4/14/2022 |
| 7084 | Bolder Surgical [Hologic] San Diego, CA Scientist 1 M.S. Molecular Biology, Chemistry, Biochemistry or related field. Exp: 1-3 years |
Hologic is seeking a Scientist 1 responsible for initiating, directing and executing scientific research and/or development strategies. | 4/14/2022 |
| 7085 | Wave Life Sciences Lexington, MA Sr. Research Associate / Associate Scientist, Oligonucleotide CMC BS or MS in Chemistry or related Exp: 1-3 years |
This individual will be responsible for the synthesis, purification, Tangential Flow Filtration (TFF), Lyophilization, analysis and characterization of oligonucleotides. This position will support CMC activities in multiple programs, technology transfer and development services. The successful applicant will also contribute to the development of novel process technologies and IPs. Prior knowledge or experience of nucleic acids is a plus. | 4/11/2022 |
| 7086 | Wave Life Sciences Cambridge, MA Associate Scientist/Scientist, Medicinal/Organic Chemistry BS or MS or PhD in Organic or Medicinal Chemistry Exp: 0-2 years |
This individual will be responsible for planning, designing, and executing multi-step synthesis including purification and compound characterization. Active collaboration with colleagues across disciplines, participation in project team meetings, and contribution toward creative problem solving are all encouraged. | 4/11/2022 |
| 7087 | Wave Life Sciences Lexington, MA Associate / Senior Associate Scientist, Preclinical Development MS in Cellular or Molecular Biology, or related Exp: 1-3 years |
The successful candidate will be an integral member of the Investigative Toxicology group and contribute to expanding our neuroimmunology and cellular/molecular biology capabilities to support safety assessment of our PRISM platform and multiple projects in the portfolio. This position reports to a Senior Scientist on the team and will collaborate cross-functionally with other scientists. The ideal candidate has a background in neurobiology and/or immunology. | 4/11/2022 |
| 7088 | Alta Sciences Everett, WA Research Associate, Small Animal Unit BS or BA in science Exp: 0+ years |
You will learn to perform technical procedures to support advancements in pharmaceutical development. In this position you will learn and perfect complex procedures including learning the skills to operate laboratory equipment, specimens collection techniques and data acquisition. At Altasciences Preclinical Services, we work with many different small animal models: rats, mice, guinea pigs and rabbits and you will have the opportunity to become a proficient, highly skilled expert in this field | 4/11/2022 |
| 7089 | Alta Sciences Everett, WA Research Associate I, Formulations BS in science Exp: 0-1 years |
Primary responsibilities include performing basic test and control article formulation, dose preparation and dispensing. Also responsible for receiving test and control article materials and maintaining chain of custody documentation associated with test and control materials, including inventory control. | 4/11/2022 |
| 7090 | Alta Sciences Remote, Medical Writing Associate I BS in Pharmacology or related Exp: 0+ years |
Responsibilities: Develop, amend and revise informed consent forms and protocols and any other supporting documents for studies of simple to moderate complexity; Work closely with team members to handle client/institutional review board (IRB) comments; Assist in entry of protocol-related information into the computer management system required for clinical conduct, as required | 4/11/2022 |
| 7091 | Alta Sciences Everett, WA Entry Level Life Science Jobs BS in science Exp: 0 years |
Altasciences Preclinical Seattle is growing quickly and is offering full time opportunities for experienced, entry level, and recent graduates interested in an exciting career in Life Science Research! Possible positions include: Animal Care Technicians, Research Associates (In vivo, Analytical Biology, and Formulations), Pathology Associates, Laboratory Assistants, Specimen Processing Technicians, Study Supervisors, Bioanalytical Scientists, Study Coordinators, Histology Technicians | 4/11/2022 |
| 7092 | Alta Sciences Everett, WA Research Associate, Large Animal Unit BS or BA in science Exp: 1-2 years |
You will perform technical procedures to support advancements in pharmaceutical development. In this position you will learn and perfect complex procedures including learning the skills to operate laboratory equipment, specimens collection techniques and data acquisition. At Altasciences Preclinical Services, we work with many different large animal models: non-human primates, swine and canine and you will have the opportunity to become a proficient, highly skilled expert in this field. | 4/11/2022 |
| 7093 | Alta Sciences Everett, WA Pathology Associate BS or BA in science Exp: 0.5-1 years |
The Pathology Associate I will perform necropsies, tissue trimming and processing on all pathology related study materials as specified in company protocols and SOPs. | 4/11/2022 |
| 7094 | Alta Sciences Everett, WA Manufacturing Associate BS or BA in science Exp: 1+ years |
The Manufacturing Associate is responsible for performing daily manufacturing operations and maintenance, cleaning of all manufacturing equipment, facility upkeep and assists with materials management. | 4/11/2022 |
| 7095 | Frontage Laboratories Exton, PA Scientist/Associate Scientist - Cell Culture BS or MS in molecular biology, biochemistry, biophysics, immunology, or related Exp: 1+ years |
This is a bench scientific position for a competent and hardworking scientist with experience in protein purification and/or labeling of protein reagents. The person will be responsible labeling of reagents (protein and antibodies), purification and characterization including concentration estimation, SDS-PAGE, SE-HPLC, endotoxin estimations etc. He/she will be responsible for the quality of final product, record keeping and interacting with end user. The position will require excellent communication skills, and basic computer skills. | 4/11/2022 |
| 7096 | Frontage Laboratories Exton, PA Scientist/Associate Scientist - Molecular Biology BS or MS in molecular biology, biochemistry, biophysics, immunology, or related Exp: 1+ years |
This position will work with Client’s Lead Engineering Group who designs lead biologic candidates by incorporating state-of-the-art design concepts into multispecific antibodies. In this position, the staff will be an integral member of the technology savvy Lead Engineering Group that delivers “Therapeutic Biological Molecules” into the pipeline. The position offers an opportunity to not only engage in the discovery and molecular engineering of biotherapeutics but also develop new processes and technologies for therapeutic discovery. | 4/11/2022 |
| 7097 | Frontage Laboratories Exton or Spring House, PA Scientist/Associate Scientist - Protein Biology BS or MS in life science or related Exp: 1+ years |
This is a bench scientific position for a competent and hardworking scientist with experience in protein purification and/or labeling of protein reagents. The person will be responsible labeling of reagents (protein and antibodies), purification and characterization including concentration estimation, SDS-PAGE, SE-HPLC, endotoxin estimations etc. He/she will be responsible for the quality of final product, record keeping and interacting with end user. The position will require excellent communication skills, and basic computer skills. | 4/11/2022 |
| 7098 | Frontage Laboratories Chicago, IL Analytical Chemist BS in Chemistry Exp: 0-3 years |
Responsibilities: Methods transfer/development and validation; Determination of analytes in dose formulations and accurate preparation of formulations (e.g., solutions, suspensions, etc.) to be used in toxicology studies; Operation of analytical instrumentation including HPLC, GC, and UV/VIS; Strict adherence to Good Laboratory Practice | 4/11/2022 |
| 7099 | Frontage Laboratories Hayward, CA Associate Scientist, Bioanalytical Services BS or BA in science Exp: 1-5 years |
Responsibilities: Independently set up bioanalytical runs; Prepare samples manually or via Hamilton Liquid Automation; Track samples and reagents appropriately in Watson Laboratory Information Management System (LIMS) or Mosaic reagent management system; Contribute bioanalytical expertise to the development of relevant systems or suggest improvements to these systems; May need to handle, process biological tissues, including potentially infectious matrices. | 4/11/2022 |
| 7100 | Frontage Laboratories Chicago, IL Assistant/Associate Toxicologist BS in animal/veterinary science, biology, or related Exp: 0-3 years |
Responsibilities: Duties include handling, dosing, weighing, and observing animals; Recording and summarizing data; Knowledge of Good Laboratory Practice Regulations (GLPs) as well as past experience in the conduct of toxicology studies or animal handling is a plus. | 4/11/2022 |
| 7101 | Endotronix Remote, Data Engineer BS in Computer Science, Data Science, Engineering, or related Exp: 1+ years |
We are looking for an enthusiastic, technically & analytically minded individual to assist in developing our next generation data infrastructure and analytics tools to help clinicians better care for their HF patients leveraging our new products. Our aim is to enable proactive & remote management of patient’s heart failure to reduce the impact it has on their quality of life. As a member of our Data Science team, you’ll work alongside our experts to help shape the future of heart failure management. | 4/11/2022 |
| 7102 | UBC Blue Bell, PA Safety Data Associate BS in science or health-related field Exp: 0 years |
Is responsible for the monitoring on a daily basis of the PV mailboxes, fax machines SharePoint/portals and acknowledging receipt of safety case reports; Is responsible for Book-in, duplicate check and accurate full Data Entry of safety case reports into safety database in a timely manner; Generates draft case narrative as assigned by UBC PV Management; Produces assigned work at high quality and according to timelines. | 4/11/2022 |
| 7103 | Sagent Pharmaceuticals Raleigh, NC Validation Engineer BS in science or engineering Exp: 0+ years |
Responsibilities: Author validation protocols and final reports; Execute requalification and validation protocols; Organize and maintain validation documentation; Track projects for on time delivery; Calibration and use of Kaye validators; Work in all areas of manufacturing maintaining gown qualification and proper aseptic technique | 4/11/2022 |
| 7104 | Sagent Pharmaceuticals Raleigh, NC Packaging Engineer BS in Packaging Engineering or related Exp: 1 year |
Responsibilities: Conduct engineering assessment of new product packaging; Evaluate and determine if new product packaging falls within approved matrix; Determine if any unusual packaging elements are part of new product (such as tamper evident feature for non-vial containers.) Make marketing and project management aware of special features and potential effect on packaging approval; Coordinate completion of packaging specs with CMOs (get product details, initiate drafts, follow up, insure completed correctly, forward for internal approval). | 4/11/2022 |
| 7105 | Sagent Pharmaceuticals Raleigh, NC Specialist I, MQA BS in Life Sciences or Physical Sciences Exp: 1-5 years |
This position will provide quality oversight to all manufacturing areas to ensure product quality and SOP/GMP compliance at the Raleigh Manufacturing Facility. Has extensive knowledge of the manufacturing process and routinely evaluates and resolves process issues in cooperation with Production and support personnel to ensure product safety. Works closely with Production personnel to complete on-the-floor, in-process batch record review, resolve all batch related issues, and ensure proper good documentation practices. | 4/11/2022 |
| 7106 | Wugen St. Louis , MO Associate Scientist, In Vitro BS or MS in Biology, Engineering, or related Exp: 1+ years |
This scientist will work closely with fellow synthetic biology scientists to develop and evaluate the activity and efficacy of novel candidate cellular therapeutics. This candidate will be responsible for the execution and analysis of preclinical studies and will play a vital role in the translation of our novel cell therapies to the clinic. This position is available in St. Louis, MO and San Diego, CA. | 4/12/2022 |
| 7107 | Wugen San Diego, CA Associate Scientist, In Vivo BS or MS in Biology, Engineering, or related Exp: 1+ years |
This candidate will be responsible for establishing and performing in vivo testing to guide the selection and development of cellular therapies using mouse models of cancer. This position is available in St. Louis, MO and San Diego, CA. | 4/12/2022 |
| 7108 | 1910 Genetics Boston, MA Research Associate, Biology BS or MS in Biology, Cell Biology, Molecular Biology, Biochemistry, Pharmacology, or related Exp: 0-3 years |
Responsibilities include: Executing high throughput screening (HTS) assays in strict accordance with the NIH NCATS Assay Guidance Manual; Developing and validating HTS biochemical assays for characterizing the activity and selectivity of potential drug candidates; Developing and validating HTS cell-based assays for characterizing the activity, selectivity, and cellular permeability of potential drug candidates | 4/12/2022 |
| 7109 | 23andMe Sunnyvale, CA Research Associate BS in Biology or related Exp: 1+ years |
Responsibilities include: Collaborate with colleagues in research, therapeutics, marketing, engineering, product, business development, and customer care to develop and implement recruitment, enrollment, and engagement strategies; Take meeting minutes, track action items, organize documentation, issue compensation to research participants, track study metrics, and route study materials for stakeholder approval and IRB submission; Serve as a patient/participant liaison; etc. | 4/12/2022 |
| 7110 | 23andMe Sunnyvale, CA Research Associate, Research Ethics BS degree Exp: 1-2 years (preferred) |
This person will join a team of Regulatory Scientists and will assist with the IRB submissions of research protocols, manage project-tracking systems, and contribute to compliance-related activities. This is an exciting opportunity to learn about the ethical and regulatory components of the personal genomics industry and take an active role in the protection of research participants who are contributing to ground-breaking genetics research. | 4/12/2022 |
| 7111 | A2 Biotherapeutics Los Angeles, CA Research Associate - Translational Science BS or MS in biology, immunology, biotechnology, or a related science Exp: 1-2 years |
This role will help to develop our patient sample analysis capabilities for our upcoming clinical trials. Tasks will involve, but not be limited to: DNA isolation, cell culture, T cell manipulation and characterization, and executing a variety of immuno- and cell-based assays. | 4/14/2022 |
| 7112 | A2 Biotherapeutics Los Angeles, CA Quality Control Associate (June 2022 Start) BS or MS in Biology, Biochemistry, Bioengineering, or related Exp: 1+ years |
We are seeking a highly motivated Quality Control Associate to join our team reporting to the Senior Quality Control Associate. In this role, you will execute the analytical quality control testing studies to support assay characterization and qualification and Phase 1 manufacturing for cell therapy – collaborating with internal partners and external CMOs / CROs. | 4/14/2022 |
| 7113 | Abbott Sylmar, CA Engineer I BS in Engineering or related Exp: 0-2 years |
Performs analyses to develop design specifications and performance requirements. Provides technical information concerning manufacturing or processing techniques, materials, properties and process (advantages/limitations) engineering planning. Selects techniques to solve problems and make sound design recommendations. | 4/14/2022 |
| 7114 | Abbott Pleasanton, CA Test Engineer I BS in Engineering or related Exp: 0-3 years |
We are seeking a Test Engineer to support our Manufacturing Sustaining Test Engineering Group . This includes but not limited to, design and develop new software and hardware to test new products. Investigates and resolves production problems involving test equipment software and hardware. Apply engineering and scientific principles to the evaluation and solution of technical problems. | 4/14/2022 |
| 7115 | Abbott Westfield, IN Facilities Engineer I BS in science or engineering Exp: 0-2 years |
Plans, designs, and supervises the construction of new, or existing, facilities in support of Company goals by utilizing available resources in the most efficient and effective manner possible while complying with time and budget constraints. Is in alignment with business goals as determined by manager and Senior Facility Engineer. | 4/14/2022 |
| 7116 | Abbott St. Paul, MN Packaging Engineer I BS in Packaging Engineering or Mechanical Engineering Exp: 0-2 years |
Support packaging and labeling processes for established product lines. Develop packaging and labeling for new products. | 4/14/2022 |
| 7117 | Abbott Plymouth, MN R&D Engineer I - Electrophysiology BS in Mechanical Engineering, Biomedical Engineering or related Exp: 1+ months |
As R&D Engineer I, you will be part of a product development team focused on delivering future Electrophysiology catheters to the global healthcare market. This role will potentially involve a range of responsibilities including but not limited to testing and data analysis, design concept generation, requirement development, and test method development and validation. | 4/14/2022 |
| 7118 | Abbott Minnetonka, MN Engineer I, R&D BS in Mechanical Engineering, Biomedical Engineering or related Exp: 1+ years |
Responsible for providing engineering support to device manufacturing operations. Develops and implements efficient, cost-effective process improvements. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study. Applies engineering and scientific principles to the evaluation and solution of technical problems. | 4/14/2022 |
| 7119 | Abbott Abbott Park, IL Associate R&D Scientist - Immunoassay BS or MS in Life Sciences or Physical Sciences Exp: 1 year |
Responsible for implementing and maintaining the effectiveness of the quality system; Conducts experiments, accomplishes established milestones and summarizes data; Recommends options for other experiments; Presents data within team; Troubleshoots instrumentation or experiments; recognizes and assists with technical problems | 4/14/2022 |
| 7120 | AbbVie Branchburg, NJ Biological Research Associate II/III MS in Biological Science or Materials Science Exp: 1+ years |
The successful candidate will contribute to projects aimed at developing, evaluating and characterizing biologic and synthetic implantable materials. Knowledge of various tissue processing, cellular & molecular biology techniques (cell culture, immunohistochemistry, ELISA, etc.) and/or biomaterial characterization techniques (DSC, SEM, etc.) is preferred. | 4/14/2022 |
| 7121 | AbbVie Worcester, MA Associate Data Engineer BS in Engineering or Computer Science Exp: 0-2 years |
The Associate Data Engineer will be responsible for combining their analytical and problem-solving skillsets to help design, implement, and maintain data workflows for AbbVie Bioresearch Center’s Connected Plant program. A successful candidate will be someone who can work independently and see projects from start to finish, can interact directly with stakeholders, and excels in applying novel approaches to complex data problems. | 4/14/2022 |
| 7122 | ABS Wilmington, DE Biorepository Scientist I BA, BS, or MS in biological sciences Exp: 0+ years |
This position is involved in the management of biospecimen inventory, procurement and distribution of samples as is necessary to meet client project demand. This position requires monitoring and maintenance of lab equipment including ultra low temperature freezers and alarm system. Participation in various cellular isolation preparations is also required. | 4/14/2022 |
| 7123 | ABS Wilmington, DE Cell Culture Scientist BA, BS, or MS in biological sciences Exp: 0+ years |
The position involves maintenance of cell culture lines to include thawing, expanding, harvesting and freezing lines. Strict quality control guidelines of all products coming from cell culture must be monitored and adhered to. Proper and aseptic maintenance of cell culture and production laboratory is required. | 4/14/2022 |
| 7124 | Abveris Quincy, MA Research Assistant - Protein Analytics BS or MS in Biology, Biochemistry, Biochemical Engineering, or related Exp: 1-3 years |
Using state-of-the art technologies and workflows, this Research Associate would work with the Protein Analytics team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 4/14/2022 |
| 7125 | Strateos Remote, Junior Software Engineer (Backend) BS in computer science or related Exp: 1-2 years |
Activities include: Working with our scientists and operators to identify and define best practices for writing protocols that accurately capture scientific intent while being reliably schedulable Integration of new devices, continuous optimization and improvement of the services and components, implementing fault-tolerance and fail-fast strategies in order to scale and thereby enhancing the modeling, scheduling, and dispatching of ever more complex protocols | 4/3/2022 |
| 7126 | Sunrise Pharma Rahway, NJ Regulatory Affairs Associate MS in Pharmaceutical Manufacturing, Pharmacy, Regulatory Affairs, or Quality Assurance Exp: 6 months |
Responsibilities include creating & implementing labels for OTC & ANDA submissions, assist in ANDA submissions using eCTD submission software, prepare & maintain annual reports, SOP, deviations & OOS reports, review product complaints & queries & support in developing regulatory strategies & launch OTC products. | 4/3/2022 |
| 7127 | Symbiotic Research Mount Olive, NJ Entry-Level Chemist BS in chemistry or related Exp: 0 years |
We have an opening for a junior level scientist to support our Plant Metabolism and Environmental Fate research groups. Strong chemistry background is highly desired. Experience in HPLC, purification, isolation, wet chemistry and HPLC-MS is a plus. Qualified applicants must have minimum GPA of 3 and be able to work in a team environment. | 4/3/2022 |
| 7128 | Systimmune Redmond, WA Research Associate - Antibody Discovery MS in science or engineering Exp: 1+ years |
We are seeking a highly motivated and detailed oriented research associate with background in immunological techniques to join our Antibody Discovery department. The successful candidate will participate in all aspects of the generation and characterization of antibodies. This will involve careful experiment planning in collaboration with the lead scientist and extensive hands-on bench work. | 4/3/2022 |
| 7129 | Talus Bio Seattle, WA Research Associate BS in biological sciences or chemistry Exp: 1+ years |
Responsibilities: Culture of human cell lines and cell treatment with candidate drug compounds; Extraction and preparation of proteins for analysis by mass spectrometry proteomics; Development and optimization of standard operating procedures for new experimental workflows; Execution of experimental and data analysis support for internal and external projects; Training and mentorship of new assistants as needed. | 4/3/2022 |
| 7130 | Tectonic Therapeutic Watertown, MA Research Associate - Cell Pharmacology BS in Biology, Pharmacology, Biochemistry or related Exp: 1-3 years |
Responsibilities: Perform transfections in mammalian cells and generate stable cell lines; Characterize and validate gene expression by qPCR, western blot and FACS techniques; Develop/ establish functional cell-based signaling assays and facilitate screening of novel therapeutics targeting GPCRs in 96-/ 384-well plate formats. Primarily luminescence and fluorescence-based assays, including HTRF will be used; Analyze, interpret, and present data in lab meetings; Maintain a detailed and accurate lab notebook | 4/3/2022 |
| 7131 | Tectonic Therapeutic Watertown, MA Research Associate - Protein Sciences BS in Biology, Biochemistry, or related Exp: 1-3 years |
Responsibilities: Perform transient transfections of human endothelial kidney (HEK) cells in suspension; Maintain seed stocks and active cultures for timely transfection of new constructs with clear documentation of cell health across the stock lifetime; Produce and maintain plasmid stocks with E. coli plasmid production and Maxiprep plasmid purification; Isolate supernatants for secreted proteins | 4/3/2022 |
| 7132 | Tegmine Therapeutics South San Francisco, CA Biochemistry Research Associate BS or MS in Biology, Biochemistry, or related Exp: 1+ years |
We are seeking a Research Associate to join our growing Discovery Proteomics team. This is an early discovery role and will support our target identification and validation efforts. Utilizing state of the art mass spectrometry technologies you will characterize modifications of purified protein targets and help identify new protein targets from patient derived samples. Building upon established methods, you will have the opportunity to test and develop new protocols and gain experience in a range of techniques as we develop additional ADC therapies. | 4/3/2022 |
| 7133 | Terray Therapeutics Pasadena, CA Technician: Ultra-Dense Microarray Preparation and Imaging BS in Biology, Chemistry, or related Exp: 0 years |
Terray is seeking technicians on our microarray preparation and imaging team. This team is the backbone of everything we do at Terray, as they are responsible for producing the ultra-dense microarray chips that power our entire discovery effort. The technicians are responsible for each key step along this process. | 4/3/2022 |
| 7134 | Terray Therapeutics Pasadena, CA Associate Scientist: Chemistry MS in Organic Chemistry or related Exp: 0 years |
Terray is seeking an associate organic chemist to be a key part of our chemistry team. The associate scientist will be primarily responsible for resynthesis of hit compounds and will also support reaction development and library synthesis as needed. | 4/3/2022 |
| 7135 | Tevard Biosciences Cambridge, MA Research Associate/ Sr. Research Associate - In Vivo Pharmacology BS or MS in Neuroscience, Physiology, Molecular/Cellular Biology, or related Exp: 1+ years |
In this position, you will collaborate with expert scientists in the in vivo pharmacology group to prioritize and demonstrate functional proof of concept for Tevard’s therapeutic tRNA lead candidates. The research associate will be responsible for conducting experiments to quantify animal behavior and physiological readouts in rodent models of rare CNS diseases as well as other indications. Hands-on experience working with rodent animal models (mouse or rat) – including animal handling and husbandry is required. | 4/3/2022 |
| 7136 | Exact Sciences Cambridge, MA Research Associate I - Protein (Temporary) BS in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related Exp: 1+ years |
This position will support the development and validation of protein assays from the feasibility stage through commercialization, in addition to the processing and screening of samples and specimens. The candidate will work closely with the sample processing, assay development, automation, and data science teams to support the product development efforts towards potential diagnostics assays. This is a temporary position with an expected duration of 6 months. | 4/3/2022 |
| 7137 | Exact Sciences Cambridge, MA Research Associate II BS in cellular and/or molecular biology, biochemistry, genetics, cancer biology or related Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day-to-day experimentation and is responsible for the execution of bench experiments and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 4/3/2022 |
| 7138 | Exact Sciences Madison, WI Laboratory Service Engineer I - Sunday - Wednesday, 2:00pm - 1:00am Shift BS in Engineering, Technology, Molecular Biology, Electronics, or related Exp: 0 years |
The Laboratory Service Engineer I (LSE I) is responsible for the Instrument and Automation Services of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Engineers (LSE) and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. The LSE I may work continuously with other LSEs and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. | 4/3/2022 |
| 7139 | Exact Sciences Madison, WI Research Associate II, Product Development BS in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day-to-day experimentation and is responsible for the execution of bench experiments and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 4/3/2022 |
| 7140 | Exact Sciences Madison, WI Research Associate I, Advanced Research and Technology BS in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related Exp: 0 years |
The Research Associate I, with guidance from more experienced scientists, assists in the day to day experimental work that includes execution of bench experiments, and gathering and assembling of data. Working in a team setting, the Research Associate I will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 4/3/2022 |
| 7141 | Exact Sciences Cambridge, MA Laboratory Service Engineer I BS in Engineering, Technology, Molecular Biology, Electronics, or related Exp: 0 years |
The Laboratory Service Engineer I (LSE I) is responsible for the Instrument and Automation Services of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Engineers (LSE) and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. | 4/3/2022 |
| 7142 | Exact Sciences Phoenix, AZ Molecular Technologist I BS in a Biological Science or Medical Laboratory Technology Exp: 0 years |
Responsibilities: Competently carry out the laboratory’s procedures for specimen handling and processing according to the standard operating procedures (SOPs); Perform testing for the downstream molecular analysis of disease using advanced techniques and equipment according to the SOPs; Maintain detailed records of testing and any corrective actions in adherence to CLIA regulations; escalated errors are to be performed with and assisted by the Supervisor; Calibrate and perform routine maintenance on equipment to ensure proper functioning according to the SOPs | 4/3/2022 |
| 7143 | Tissuetech Miami, FL R&D Validation Engineer BS in Engineering, Biology, Chemistry, Biochemistry, or related Exp: 1 year |
The incumbent will be responsible performing basic to moderate level engineering tasks to support the development of new and existing HCT/Ps, medical devices, cosmetics, and biologics as well as to support compliance of the Research and Development laboratory to FDA and ISO standards. Primary responsibilities will include coordinating and supporting activities for product development; to include design verifications, process validations, and stability studies; as well as to support the validation/qualification of laboratory computer systems | 4/4/2022 |
| 7144 | Treeline Biosciences San Diego, CA Analytical Research Associate BS or MS in Chemistry, Analytical Chemistry, Toxicology, or related Exp: BS: 1-3 yrs. MS: 0+ yrs. |
As a Research Associate in Analytical Chemistry, you will work closely with Analytical Scientists and Medicinal Chemists to assess the purity of intermediates and final compounds to facilitate drug discovery and development. You will also contribute to the method development and validation for compound stability and other assays. | 4/4/2022 |
| 7145 | Treeline Biosciences San Diego, CA Senior Research Associate - Medicinal Chemistry BS or MS in Medicinal Chemistry or related Exp: 0-8 years |
The Sr. Research Associate of Medicinal Chemistry is primarily responsible for designing and executing the synthesis of small molecules as potential oncology therapeutics. A demonstrated success of organic synthesis execution and expertise is required. The researcher will also evaluate the structure activity relationships of evolving chemical matter in order to optimize the potency, pharmacokinetics, safety, and in vivo efficacy of potential small molecule oncology drugs. | 4/4/2022 |
| 7146 | Treeline Biosciences Watertown, MA Senior Research Associate - Medicinal Chemistry BS or MS in Medicinal Chemistry or related Exp: 0-8 years |
The Sr. Research Associate of Medicinal Chemistry is primarily responsible for designing and executing the synthesis of small molecules as potential oncology therapeutics. A demonstrated success of organic synthesis execution and expertise is required. The researcher will also evaluate the structure activity relationships of evolving chemical matter in order to optimize the potency, pharmacokinetics, safety, and in vivo efficacy of potential small molecule oncology drugs. | 4/4/2022 |
| 7147 | Tune Therapeutics Seattle, WA Associate Engineer, Viral Vector Development MS in Biochemistry, Bioengineering, Chemical Engineering, or related Exp: 1-3 years |
We are seeking a highly motivated Associate Engineer or Engineer in process development to help realize the promise of epigenetic programming. In this role, you will be responsible for assisting in the development of viral vector delivery platforms to advance multiple epigenetic therapy programs through preclinical and clinical development. You will participate in exploration of next generation AAV capsid technologies and drive their adoption. In addition, you will work with a dynamic and fast-paced group to drive delivery. | 4/5/2022 |
| 7148 | Tyber Medical Bethlehem, PA Production Planner BS in Engineering, Business Management, or Supply Chain Management Exp: 0 years |
The Production Planner acts as a critical interface between the customers and Tyber Medical. The responsibilities include scheduling, planning, expediting, inventory management, and communicating requirements to meet demand. The Production Planner is responsible for releasing orders to the production floor based on WIP targets and shipping commitments to the customer. Production Planner’s scope includes monitoring inventory levels, regularly providing production status updates to management, and facilitating the timely delivery of products to customers. | 4/7/2022 |
| 7149 | Unity Biosciences South San Francisco, CA Research Associate 1 or 2 BS or MS in science Exp: BS: 1-4 years, MS: 1-2 years |
The position requires a self-motivated individual seeking a hands-on, lab-based role using in vivo animal models and in vitro methodologies to contribute to specific project goals as part of a dynamic team. The duties of the job include animal handling/dosing, experimental design and execution, analysis/interpretation of data, downstream sample generation/ samples processing, and presentation (verbal/written) of findings at team meetings. | 4/7/2022 |
| 7150 | Unity Biosciences South San Francisco, CA Research Associate 1 or 2, In Vitro Pharmacology MS in science Exp: 1 year |
This is a lab-based position focused on performing a variety of in vitro assays including, cell-based assays, biochemical assays, and MSD-based ELISA assays, and other molecular biology techniques. The candidate will be responsible for experimental design, execution, analysis, and presentation to the project team. This individual will play a key role in supporting a advancement of large molecule candidate through in vitro studies. | 4/7/2022 |
| 7151 | Astellas Pharmaceutical Seattle, WA Laboratory Assistant I BS in Life Sciences Exp: 1-2 years |
The primary purpose of the Laboratory Assistant position is to ensure the efficient operations of designated laboratory spaces, to include general lab organization, proper stocking of lab supplies and cleanliness. This position will work in a team environment, directly supporting the lab activities of the assigned laboratory room/s. | 4/7/2022 |
| 7152 | Astellas Pharmaceutical Seattle, WA Research Associate I, Cell Editing BS in science Exp: 0-3 years |
The primary purpose of the Research Associate I for Cell Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This entry-level Research Associate role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. | 4/7/2022 |
| 7153 | Astellas Pharmaceutical Seattle, WA Research Associate II, Vector Production MS in Life Sciences Exp: 0-2 years |
This individual will contribute to the further molecular engineering for our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to assist with Adeno-Associated Virus production and the development and execution of molecular assays to characterize our proprietary gene edited cells. | 4/7/2022 |
| 7154 | Vaxart South San Francisco, CA PD Associate, Downstream BS or MS in Biological Sciences, Chemical Engineering, Chemistry, Biochemistry, or related Exp: 0-8 years |
The PD Associate for Downstream is responsible for understanding, executing, and reporting downstream processes with a focus on development and manufacture of Ad5 vectors used for oral vaccines. Under supervision from a Senior Scientist, evaluate existing downstream methods and develop new methods appropriate for improved yield, larger scale, and improved or sustained product quality in the production of Ad5 viral vectors for use in an oral vaccine. | 4/7/2022 |
| 7155 | Vaxcyte San Carlos, CA Associate Engineer, Polysaccharide Downstream Process Development MS in Chemical Engineering, Biochemistry, or related Exp: 1+ years |
Vaxcyte is looking for an energetic and talented Associate Engineer to contribute to the Polysaccharide development and manufacturing group within the CMC team. The successful candidate will have some laboratory experience developing processes related to biotechnology, biopharmaceuticals, or vaccine industries. The candidate will be eager to utilize and learn new laboratory skills as this person will be responsible for collaboration on experimental design and execution of experiments to further the polysaccharide development and manufacturing programs. | 4/7/2022 |
| 7156 | VGXI Inc. The Woodlands, TX Environmental Monitoring Technician BS or Associates in science Exp: 1-3 years |
The primary responsibility of Environmental Monitoring Technician is to perform all EM monitoring and related testing; water sampling and testing. Responsibilities also could include in-process and release testing of products manufactured at VGXI. Set-up, organization, and day-to-day operations of a Quality Control Lab are also required. | 4/7/2022 |
| 7157 | VGXI Inc. The Woodlands, TX Quality Control Technician BS or Associates in science Exp: 1-3 years |
The Quality Control Technician is responsible for in-process and release testing of products manufactured at VGXI. Responsibilities also include environmental monitoring of the production areas and raw material quarantine and release. Set-up, organization, and day-to-day operations of a Quality Control Lab are also required. | 4/7/2022 |
| 7158 | VGXI Inc. The Woodlands, TX Quality Assurance Specialist BS degree Exp: 0 years |
Responsibilities include: Assembling of batch documentation related to disposition products; Processing CAPAs; Performing routine internal audits of manufacturing and quality control processes; Maintaining supplier files; Performing supplier audits; Maintaining audit files; Responsible for proper documentation of equipment; Conducting training for new employees; Assist in development of quality system SOPs | 4/7/2022 |
| 7159 | VGXI Inc. The Woodlands, TX Validation Specialist BS in science or engineering Exp: 1-3 years |
Support process and product quality programs including process, testing, and software validation, equipment calibration programs, and process monitoring activities by writing simple verification/validation documents, executing qualification tests, compiling data, drafting summary reports, and reviewing validation documentation to ensure products are manufactured in accordance with applicable regulatory guidelines, manufacturer’s specifications, client’s specifications, and VGXI’s requirements. | 4/7/2022 |
| 7160 | Viant South Plainfield, NJ Manufacturing Engineer BS in Engineering Exp: 0-2 years |
Assists in developing, implementing, and improving new and existing manufacturing processes for medical device products. Provides engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with company’s procedures. Supports current production, providing technical solutions to meet quality, safety, cost, and efficiency goals. Supports Continuous Improvement initiatives. Position will be assigned either to the New Product Introduction Group or the Sustaining Engineering Group as required, while also supporting projects related to the greater team and company effort. | 4/7/2022 |
| 7161 | Viant Fremont, CA Product Development Engineer BS or MS in Bioengineering, Biomedical Engineering, or Mechanical Engineering Exp: 0 years |
Come join our rapidly growing team of creative, high-energy engineers and help make a positive impact on people’s lives. Contribute to the development of innovative, state of the art and next-generation products improving the quality of people health. Expertise focused in two main product categories: Single-use, minimally-invasive interventional catheter products and Active implantable, insertable or wearable neuro-modulation devices. | 4/7/2022 |
| 7162 | Vivex Biologics Miami, FL Process Engineer I BS in Biomedical Engineering or related engineering Exp: 1-3 years |
The Process Engineer I is responsible for evaluating and improving manufacturing processes to reduce cost, improve yields and reduce variation. This position performs equipment qualifications and process validations. Process Engineers also participate in technology transfer to ensure the processes necessary for new products are effectively translated to manufacturing from R&D. Process Engineer I makes use of statistical analysis methods, critical thinking, process development, and scaling principles to achieve our objectives. | 4/7/2022 |
| 7163 | Vividion Therapeutics San Diego, CA Research Associate II, Biochemistry (TOFMS) BS or MS in Biochemistry or related Exp: 1+ years |
Responsibilities include: Perform routine maintenance, calibration and troubleshooting of mass spectrometers to keep instruments delivering high quality data; Experience characterizing protein-small molecule complexes by MS to support screening of covalent small molecules and determining rates of engagement; Perform optimization of liquid chromatography to obtain robust and high quality spectra of purified protein, peptides and small molecules | 4/7/2022 |
| 7164 | Advanced Cell Diagnostics [bio-techne] Minneapolis, MN Research Associate / Advanced Research Associate, Molecular Biology Bachelors degree in a scientific discipline or equivalent Exp: 0-2 years |
Key Responsibilities Molecular biology techniques including DNA isolation, PCR, and cloning Expression of recombinant antibodies and other proteins Protein analysis using SDS-PAGE, Western Blot, and ELISA Small-scale protein purification of immunogens and controls Written and electronic record-keeping of experimentation Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job. Performs additional duties as assigned. | 4/5/2022 |
| 7165 | Advanced Cell Diagnostics [bio-techne] Newark, CA Research Associate, R&D BS in molecular biology, biochemistry, cell biology or related field Exp: 1 year |
We seek a highly motivated and creative research associate to join our R&D team. You will work within a highly dynamic group and be responsible for improving current products and developing new products based on RNAscope technology. | 4/5/2022 |
| 7166 | Advanced Cell Diagnostics [bio-techne] San Marcos, CA Research Associate (Temporary) Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field preferred Exp: 0-2 years |
This position is responsible for the developing and or formulation of controls, calibrators, working solutions, and intermediates in the production and development of Bio-Techne's various product lines. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio | 4/5/2022 |
| 7167 | Advanced Cell Diagnostics [bio-techne] Minneapolis, MN Research Associate - Cell Culture Development Bachelor’s degree. Exp: 0-2 years |
A Research Associate is responsible for development of cell culture protocols for new recombinant protein products. This includes screening clones and testing growth conditions in bioreactors and other culture formats, in small to medium scale. It may also include cooperation with the molecular biology group in creation of new clones and clone libraries, creation and characterization of new cell lines, and screening studies in search for novel protein product targets. | 4/5/2022 |
| 7168 | Advanced Cell Diagnostics [bio-techne] Minneapolis, MN Research Associate Bachelor’s degree. Exp: 0-2 years |
The Stem Cell and Gene Therapy Research Associate will be part of a team responsible for the design and development of novel products used in cell and gene therapy workflows. Major responsibilities include 2D and 3D cell culture, immunostaining, microscopy, and flow cytometry. Position will involve making chemical solutions, performing experiments, analyzing data, and optimizing assays. Preference will be given to candidates with experience in stem cell culture, immunology, flow cytometry, and microscopy. | 4/5/2022 |
| 7169 | Adverum Biotechnologies Redwood City, CA Analyst I/II (Contract) Relevant scientific degree Exp: 0-4 years |
Our Development Testing Center (DTC) team is looking to bring onboard an Analyst I/II. This individual will be a key member of the Development Testing Center, performing in-process testing of study samples. This is a contract role - 6mo to start, with extension potential. | 4/5/2022 |
| 7170 | Adverum Biotechnologies Redwood City, CA Research Associate I (Process Development) - Contract Relevant scientific degree Exp: 1-4 years |
Our Process Development team is looking to bring onboard Research Associate I/II. This individual will be a key member of the Process Development team, performing in-process testing of study samples. This is a contract role - 6mo to start, with extension potential. | 4/5/2022 |
| 7171 | Agenus Lexington, MA Research Associate – Biomarker Assay Development & Data Science BS in molecular, cellular biology or related discipline Exp: soon-to-be bachelor graduate |
The candidate will be joining a group at the interface of pre-clinical and clinical teams, supporting the translation and the reverse translation efforts. The candidate will be responsible for wet lab experiments: generation, analysis and interpretation of standard biochemical assays such as ELISA and of molecular assays such as DNA/RNA extraction; and for dry lab projects formatting big data to facilitate visualization and interpretation of the team results to inform data-driven decisions. Other responsibilities may include maintenance of cell lines and assistance with pre-clinical studies in the mouse. As a part of the team, the candidate will participate in project meetings and will be required to maintain an electronic record of their activities. The candidate will also be responsible for attending weekly group meetings and present generated results. | 4/5/2022 |
| 7172 | Agenus Lexington, MA Research Associate - Research & Discovery Location BS or MS degree in immunology, molecular and cell biology, or related discipline Exp: 1+ years |
Agenus (Lexington, MA) is looking for a talented and highly motivated Research Associate to join our Immunomodulatory Drug Discovery group. The successful candidate is expected to contribute to the discovery, research, and development of novel immunotherapeutic agents to address unmet medical needs of cancer patients. She/he will have opportunities to grow their career through acquisition of new skills, experiences, and professional relationships in a fast-paced and resource-rich environment. Our collaborative and interdisciplinary research team has a track-record of applying state-of-the-art technologies and innovative methodologies to advance cutting-edge immune-oncology (IO) medicines into the clinic. | 4/5/2022 |
| 7173 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Associate I Bachelors in a science or engineering discipline preferred Exp: zero to two (2) years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 4/5/2022 |
| 7174 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Associate I - 2nd Shift Bachelors in a science or engineering discipline preferred. Exp: zero to two (2) years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 4/5/2022 |
| 7175 | Alturas Analytics Moscow, ID Assistant Scientist Bachelor’s degree in a physical, biological or chemistry science required Exp: 1-3 years |
The Assistant Scientist provides support to other laboratory personnel through a variety of duties and tasks. This is an entry-level position used to train all Associate Scientists. | 4/6/2022 |
| 7176 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, Synthesis B.S. chemistry or biochemistry degree with excellent understanding of organic and analytical chemistry Exp: 0-2 years |
Arrowhead Pharmaceuticals has multiple Associate Chemist positions open in the Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, purification, analytical chemistry, and contributing to specific program goals. S/He will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 4/6/2022 |
| 7177 | Arrowhead Pharmaceuticals Madison, WI Associate Chemical Engineer Bachelors degree in a biomedical engineering, chemical engineering, or equivalent Exp: Entry-Level |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Chemical Engineer I in the Chemistry, Manufacturing, and Controls Group. | 4/6/2022 |
| 7178 | Astellas Pharmaceuticals Seattle, WA Research Associate I, Cell Editing BS Degree Exp: 0-3 years |
The primary purpose of the Research Associate I for Cell Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This entry-level Research Associate role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. This position will be provided training to perform all required fundamental skills to include record keeping, aseptic technique/cell culture, general lab operations, equipment use and maintenance, and some troubleshooting. Will assist with basic laboratory operations, and will keep appropriate documentation, including lab notebooks, batch documentation and experimental summaries. May assist in preparing controlled documents and data summaries. | 4/6/2022 |
| 7179 | Astellas Pharmaceuticals Seattle, WA Research Associate II, Vector Production MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the further molecular engineering for our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to assist with Adeno-Associated Virus production and the development and execution of molecular assays to characterize our proprietary gene edited cells. | 4/6/2022 |
| 7180 | Astellas Pharmaceuticals Seattle, WA Research Associate II, Cellular and Molecular Biology MS degree Exp: 0-2 years |
The primary purpose of the Research Associate II position is to assist with pluripotent stem cell culture, differentiation and characterization. This position will work primarily in a laboratory setting in collaboration with other Scientists and Research Associates. | 4/6/2022 |
| 7181 | Astellas Pharmaceuticals Westborough, MA Research Associate II / Sr. Research Associate, in vivo, Cell Based Therapies MS in animal science, biology or equivalent Exp: 0-2 + years |
We are seeking an enthusiastic and highly motivated Senior Research Associate to join R&D to develop and implement mouse pre-clinical disease models in the vivarium, and support that work with complementary in vitro cell-based assays. This individual will collaborate closely within the team and across functional groups to advance pipeline programs. | 4/6/2022 |
| 7182 | Atsena Therapeutics Durham, NC Process Development Associate Bachelor's degree in chemistry, biochemistry, biology, chemical/biomolecular engineering, or a related scientific discipline; Master’s degree preferre Exp: 1 year |
We seek a motivated self-starter at the Process Development Associate level to join the CMC team at an exciting, fast growing, and well financed company to develop ocular gene therapies. The successful candidate will be responsible for performing upstream and/or downstream process development. The position requires attention to detail and ability to multitask as there are often multiple, concurrent projects. The ideal candidate will have either mammalian cell culture experience or purification experience. Experience with gene therapy and viral vectors is also a plus along with knowledge of biomanufacturing principles. This is a lab-based position. | 4/6/2022 |
| 7183 | Atsena Therapeutics Durham, NC Research Associate Master’s degree in chemistry, biochemistry, biology or related scientific discipline Exp: 1 year |
We seek a motivated self-starter at the Research Associate level to join an exciting, fast growing and well financed company to develop ocular gene therapies. The successful candidate will work with the AAV Technology team. The successful candidate will be responsible for performing or assisting with procedures associated with the production, characterization and screening of recombinant AAV vector libraries. This will entail procedures such as molecular cloning, plasmid transfections of mammalian cell culture, ultracentrifugation, ddPCR, protein gel electrophoresis, NAb assays, analytical testing, data analysis, and method development/ qualification. The position requires attention to detail and ability to multitask as there are often multiple, concurrent projects. The ideal candidate will have prior experience with mammalian cell culture (i.e. passaging, maintaining, transfecting, harvesting cells) and other techniques including molecular biology cloning, ddPCR, western blotting, and immunohistochemistry. The ideal candidate is a fast learner, that when adequately trained quickly masters new laboratory skills and can independently execute said skills. This is a lab-based position that will entail substantial on the job training in AAV gene therapy. | 4/6/2022 |
| 7184 | Immucor Waukesha, WI Research Associate III MS Exp: 1 - 3 years |
Immucor is seeking a Research Associate III for a laboratory position in our Research & Development group. The Research Associate III performs a variety of tasks associated with the development of new products and manufacturing processes, the investigation into and implementation of product and process changes, and the transfer of new products and processes to the manufacturing departments. If your degree is in medical technology, biology, or immunology, this is a great opportunity to launch your career in assay development! This position is not eligible for sponsorship for work authorization by Immucor, Inc. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time . | 3/30/2022 |
| 7185 | KMC Systems Cambridge, MA Systems Engineer I Bachelor's degree in systems engineering, biomedical engineering or equivalent scientific discipline required. Exp: 0-1 years |
Systems engineering covers the full product lifecycle, from concept through development and deployment, and ultimately, disposal. It concentrates on the design and application of the medical and diagnostic systems. It involves looking at a design challenges in its entirety, considering all the requirements and all the variables and relating the user and technical aspects. The incumbent will assist in the design, development, testing, and analysis of products, equipment or processes; and perform a variety of assignments, under close guidance/ mentoring, requiring the application of basic engineering and scientific principles and techniques. | 3/30/2022 |
| 7186 | NorTech Life Sciences Mankato, MN Quality Engineer Bachelor's degree (B. A.) from four-year college or university Exp: one to two years |
A successful Quality Engineer is adaptable, proficient at communicating with customers and teammates, and is committed to learning and problem solving. They will assure optimum quality in manufactured products in accordance with Nortech standards and contract requirements. | 3/30/2022 |
| 7187 | PL Developments Miami, FL Analytical Scientist I BS or MS in Chemistry or equivalent combination of education and experience Exp: Entry Level |
Performs testing on raw material, in-process & finished product samples Executes method transfer, verification and validation protocols Documents all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines Evaluate and interpret the test results and other related technical documentation Writes methods and reports Performs routine lab maintenance including equipment calibration, glassware cleaning, chemical and supplies inventory management (includes ordering, cleaning and organization) Other duties may be assigned as deemed appropriate by management | 3/31/2022 |
| 7188 | PL Developments Lynwood, CA Process Engineer BA/BS degree in Engineering or related field preferred Exp: 1-2 years |
Create or modify process flow diagrams Assists with performing a variety of engineering tasks related to any of the following: process improvement, quality control, research and development, general engineering and related areas Work with operations, chemists, and other staff to understand tasks and objectives, receive direction on professional level questions and issues, and communicate results Assists with ensuring compliance with department policies and procedures and applicable laws, rules, and regulations | 3/31/2022 |
| 7189 | Sedia Biosciences Beaverton, OR Assistant Scientist B.A. or B.S. in Biochemistry, Immunology, Microbiology, Biology, Genetics or similar discipline Exp: Entry Level |
Conducts moderately complex research and development occasionally requiring independent judgement as instructed or directed by higher level R&D personnel, focused on supporting the company’s product, technology and services research and development program. Typically trains less experienced personnel in routine techniques and procedures. | 3/31/2022 |
| 7190 | Sedia Biosciences Beaverton, OR R&D Laboratory Technician Associate’s or Bachelor’s degree in a laboratory discipline (biotechnology, biology, microbiology, etc.) Exp: 1 year |
Technicians are needed for Sedia’s R&D group. Successful candidates will assist with a variety of laboratory research studies focused on verifying the performance characteristics of diagnostic tests under development. Candidates must be able to follow detailed instructions and perform experiments of moderate complexity. Consistency and attention to detail are critical, and the ability to collaboratively interact in a team environment is expected. For these roles, the initial work will involve testing lateral flow immunoassay strips for product performance and reliability. Additional functions in R&D will be determined as needed and depend, in part, selected candidate’s specific experience and skill set. | 4/1/2022 |
| 7191 | Sedia Biosciences Beaverton, OR ASSOCIATE/ASSISTANT PROTEIN SCIENTIST (R&D) Bachelor’s degree in molecular biology, microbiology, biochemistry, or a related field. Exp: 1-3 years (Assistant) |
An energetic Assistant/Associate Scientist with experience in molecular biology and/or protein chemistry is needed for an opportunity in Sedia’s R&D group. Specific job requirements may be adjusted to suit the candidate’s skills. The successful candidate will assist in the development, expression, purification, and characterization of recombinant proteins (antigens, binding domains, etc.). Additionally, the candidate will participate in assay development and process scale up activities and contribute to subsequent validation and quality assessments. The selected candidate will have demonstrated experience in molecular biology, microbiology or biochemistry with skills acquired via either previous biotechnology industry employment or an undergraduate research program. The ability to work as a member of a team in a highly cross-functional environment is essential | 4/1/2022 |
| 7192 | Tanvex BioPharma San Diego, CA Research Associate, Analytical Characterization - #1350 BS or advanced degree in analytical chemistry, chemical/biochemical engineering, biochemistry, or related disciplines. Exp: 0-3 years |
The Research Associate is a key member of the Analytical Characterization team and will be involved in supporting Tanvex’s CMC activities. The ideal candidate will have shown proficiency in hands-on analytical work and strong working knowledge in various physicochemical analyses for detailed characterization of recombinant protein therapeutics. Under the guidance of his/her supervisor, the candidate will help to develop and qualify analytical methods, and conduct characterization analysis to support regulatory filings, as well as provide analytical support for process development and method transfer activities. The candidate is also expected to be involved in drafting characterization study reports, Standard Operating Procedures, method development reports, method qualification protocols and reports, as well as to collaborate with other functional groups on significant technical matters. | 4/1/2022 |
| 7193 | Tanvex BioPharma San Diego, CA Research Associate, Purification - #1383 BS or advanced degree in chemical/biochemical engineering, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Purification Development is responsible for executing individual experiments related to all aspects of purification process development from process definition to process characterization for support of pipeline projects. Performs experiments that contribute to project goals with guidance. | 4/1/2022 |
| 7194 | Tanvex BioPharma San Diego, CA Research Associate, Cell Culture PPD - #1358 BS or advanced degree in chemical/biochemical engineering, cell biology, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Cell Culture Development is responsible for executing individual experiments related to all aspects of cell culture process development of biopharmaceuticals, including media preparation, bioreactor setup, cleaning, sterility and operation, maintaining instruments and equipment, examining data and preparing experiment reports. Applies basic engineering and scientific principles to perform trouble-shooting of processes, instrumentation, and equipment. | 4/1/2022 |
| 7195 | Utah Medical Products Midvale, UT Quality Engineer Bachelor's degree (BS) from a four-year college or university Exp: one year |
Description of Responsibilities: 1. Manages complaint handling system. 2. Schedules, conducts and/or reviews internal quality audits. 3. Maintains records of internal corrective actions, and participates in routine MRB. 4. Participates in review of R&D and manufacturing projects. 5. Gathers, prepares and presents Company Quality Assurance-related reports. 6. As assigned: develops defect criteria for use in existing products/raw materials, analyzes/investigates defect causes, inspects/tests products/raw materials to determine compliance, failure mode, etc., and participates in company-wide quality-improvement efforts. 7. Confers with all levels of management to address QA issues and coordinate activities. 8. Works well with others. 9. Attends work on all scheduled work days and during scheduled work hours, except where otherwise permitted by immediate supervisor or management, in compliance with company attendance policy. Follows all other company policies and procedures, as set forth in the Employee Handbook and elsewhere, regarding employment. 10. Performs all the essential functions of the job independently using own initiative. | 4/1/2022 |
| 7196 | Advanced Bioscience Labs Rockville, MD QA Specialist I - Client Commercial - (00226_COMPANY_1.1) B.S. in a Life Sciences discipline Exp: 0-2 years |
Ensure current Good Manufacturing Practices (cGMPs) compliance for clinical manufacturing of phase I/II/III investigational biological product, and compliance to 21 CFR Parts 210, 211, and 600 as applicable Provide Quality Assurance support to concurrent Commercial and/or Government cGMP projects Performs review of various GMP documentation to ensure completeness, accuracy, and compliance; including but not limited to: Manufacturing records, Quality Control Environmental Monitoring data, batch, and material release, specifications, SOPs, test method, GMP analytical and bioanalytical data, product labels, alarm reports, deviation investigations, CAPAs and change controls. Conducts review of Quality related documents and procedures from ABL Rockville subcontractors. | 4/1/2022 |
| 7197 | Abzena San Diego, CA QA Associate I/II - MQA Bachelor’s degree in related field. (e.g., chemistry, biological sciences, bioengineering, etc.) Exp: 1 year |
The Quality Assurance Associate I/II will support quality functions in Manufacturing Quality Assurance. Some general responsibilities area as follows: Manufacturing Quality Assurance Imbedded in production Provide real time review of batch documentation Perform housekeeping checks Review of minor deviations, initiation of Major Deviations Quality representative in production Empowered to make quality decisions in real time in line with regulations and procedures Room and line clearances Support documentation creation and initiation | 4/1/2022 |
| 7198 | Acceleron Pharma [Merck] West Point, PA Scientist Bachelor’s degree in analytical chemistry, biochemistry, or related field or Master’s degree Exp: BS: 1-3 years ; MS: 0-2 years |
We are currently seeking a self-motivated, result-driven, collaborative Scientist to contribute to our company's drug discovery and early clinical development efforts in the Absorption, Distribution, Metabolism, Excretion and Discovery Toxicology (ADME&DT) Group within Preclinical Development (PCD) at our company's Research Laboratories. This position will be based at our research labs in West Point, PA. The ideal candidate will primarily perform lab-based activities and be responsible for generating issue-driven in vitro ADME data to guide lead candidate optimization and development efforts. | 4/1/2022 |
| 7199 | Acceleron Pharma [Merck] West Point, PA Scientist Bachelor’s degree in biochemistry, analytical chemistry, or related field or Master's Exp: BS: 1+ years; MS: some experience |
We are currently seeking a Scientist to contribute to our drug discovery and early clinical development efforts in the Preclinical Development (PCD). This position will be based at our research labs in West Point, PA. The Absorption, Distribution, Metabolism, and Excretion (ADME) group within the PPDM function of our company's Research Laboratories is seeking a self-motivated, result-driven, collaborative scientist to contribute to our drug discovery and early clinical development efforts. The ideal candidate will primarily perform lab-based activities and be responsible for generating issue-driven in vitro ADME data to guide lead candidate optimization and development efforts. | 4/1/2022 |
| 7200 | Acceleron Pharma [Merck] Rahway, NJ Associate Scientist B.S. or M.S. degree in Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences or related discipline (expected no later than May 2023). Exp: |
The successful candidate will be a passionate Scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible for supporting the formulation development of new chemical entities as part of a matrix team from initial first in human formulations (suspensions, solutions, capsules, tablets) through final market formulation definition and manufacturing process robustness assessment. | 4/1/2022 |
| 7201 | Acceleron Pharma [Merck] Kenilworth, NJ Scientist-Bioassay, Cell Based Sciences, AR&D Master’s Degree Exp: 1 year’s |
We are seeking a highly motivated Scientist to join our Biologics Potency team within the Cell Based Sciences, Analytical Research and Development organization of our Research Laboratories at Kenilworth, NJ. The qualified candidate will execute routine testing, and support prequalification and robustness studies for immunoassay and cell-based assay development efforts to assess the biological activity of biologics modalities such as antibodies, multifunctional proteins, peptide therapeutics, antibody-drug-conjugates, and/or cell- or gene-therapy agents. The candidate will work with technical leaders in the group to establish these types of assays, to write and review technical reports, and to support cross-functional teams. The candidate would have good working knowledge of underlying biological mechanisms and assay principles, with experience in immunoassays and/or cell-based assays to assess the potency of drug candidates. Experience with additional techniques and technologies, e.g. flow cytometry, or lab automation, will be advantageous. The candidate will will work with technical leaders in the group to communicate results effectively in presentations to the team, and author and review documents. Experience of working in a GxP regulated laboratory environment for routine sample testing, documentation, and data verification will be a plus. Experience of working on ADC, cell- or gene-therapy drug programs will be a plus. | 4/1/2022 |
| 7202 | Acceleron Pharma [Merck] Boston, MA Associate Scientist – Automation and high-throughput protein production A minimum of a B.S./ in a relevant field (e.g. protein sciences, chemical or bioengineering, biochemistry or similar), OR upcoming expected completion Exp: 1+ years |
Protein Sciences - Boston of Our Company's Research Laboratories is seeking a Scientist-level associate to execute existing laboratory automation workflows on our high-throughput (HT, robotic antibody and protein production platform (RAPTOR). Specifically, to perform weekly expression runs for hundreds of antibodies to support early discovery efforts. In this role you will build and then use a combination of protein expression, purification, and laboratory automation skills. This role will require an eagerness to learn and an ability to work with different teams and different equipment to operate a robust high throughput protein production platform. Your efforts will be a complement and core resource to existing capabilities and will serve to expand the team’s ability to interrogate antibody/protein diversity in order to identify optimal leads. You will have the opportunity to apply your enthusiasm and technical skills as a member of Protein Sciences - Boston to support and help drive multidisciplinary biotherapeutic discovery programs. | 4/1/2022 |
| 7203 | Acceleron Pharma [Merck] Durham, NC Quality Associate Specialist Bachelor of Science degree in science field, preferably biology, microbiology, biochemistry, or equivalent Exp: (1) + years |
As part of Our Company's Quality Operations Organization, the Durham site Quality team is seeking a highly motivated individual for the Quality Operations Potency Laboratory. This position is responsible for performing lot release testing in compliance with standard operating procedures, safety, and cGMP regulations. Primary duties of this position will focus on the daily quality control lab operations. We are seeking a growth and improvement minded Quality Associate Specialist that can help drive our Strategic Operating Priorities. | 4/1/2022 |
| 7204 | Rumi Scientific New York City, NY Research Assistant MS in biological sciences or related Exp: 0+ years |
We are seeking a highly-motivated Research Assistant to join our growing team. The successful candidate will contribute to the drug discovery effort as well as the development of novel therapeutics across several areas based on a strong interdisciplinary background, as our interests range from genome editing, physical methods for tissue confinement, to machine learning approach for the analysis of high content phenotypic screens. | 3/26/2022 |
| 7205 | Sanaria Rockville, MD Research Associate, Clinical Assays and Sample Management BS in biochemistry, biological sciences, or related Exp: 0+ years |
The Research Associate will play an integral role in supporting Sanaria’s Clinical Assays and Sample Management laboratory. The Laboratory’s major responsibilities include clinical sample management, serologic antibody binding, and functional assays. This is a laboratory testing position with the major responsibilities being daily assays and laboratory maintenance tasks. | 3/26/2022 |
| 7206 | SCA Pharma Windsor, CT Microbiology Analyst BS or BA in science Exp: 0-2 years |
Our Microbiology lab plays a key role in ensuring the sterility of our facilities and our products, to ensure that only the safest medications leave our facility. As a Microbiology Analyst I, you will be responsible for supporting the Microbiology Department with data processing/entry, Environmental Microbiological testing and Filtration Testing, in addition to daily housekeeping of the laboratory. | 3/26/2022 |
| 7207 | SCA Pharma Little Rock, AK Incoming Quality Assurance Specialist BS or BA Exp: 1-3 years |
The Incoming Quality Assurance Specialist will ensure that critical and key raw materials and supplies that are received meet raw material specifications set forth by SCA Pharmaceuticals and have appropriate certificates of analysis and certificates of conformance prior to releasing to inventory. These responsibilities will be performed at the production site as well as the warehouse site. In addition, the individual in this position will be responsible for maintaining and improving existing processes, as well as assisting in the design and development of new processes. | 3/26/2022 |
| 7208 | Scholar Rock Cambridge, MA Sr. Associate Scientist BS or MS in biology or related Exp: BS: 1-3 yrs. MS: 0-2 yrs. |
This team member will have a hands-on laboratory role in establishing cell-based assays using multiple technologies to help identify novel therapeutic antibodies. The successful candidate will have a key supporting role in a collaborative small-company environment with numerous opportunities to learn and grow within the early drug discovery process. | 3/26/2022 |
| 7209 | Scholar Rock Cambridge, MA Sr. Associate Scientist II, Cell Line Engineering BS or MS in cell biology, molecular biology, biochemistry, or related Exp: 1-5 years |
Scholar Rock is seeking a talented scientist to join the Protein Sciences group and be responsible for generating stable cell lines, clonal cell line production, providing protein biochemistry support including production, and characterization of antigens and antibodies to support multiple programs within our R&D Department. This position will provide the opportunity to make visible contributions to a variety of programs while interacting with a knowledgeable and dedicated multidisciplinary team. | 3/26/2022 |
| 7210 | Sebela Pharmaceuticals Holbrook, MA QC Chemist BS in chemistry or related Exp: 1 year |
Conduct routine analytical chemistry testing using various wet chemistry and instrumentation techniques in a regulated cGMP and cGLP environment. | 3/26/2022 |
| 7211 | Sebela Pharmaceuticals Holbrook, MA QC Laboratory Technician BS in chemistry or related Exp: 0 years |
Support the QC workflow and processes in an efficient and effective manner. Provide support to QC Analysts with test preparations. Performs simple / routine chemistry tests. | 3/26/2022 |
| 7212 | Serotiny San Francisco, CA Sr. Research Associate - Cell Therapy MS in science or engineering Exp: 1+ years |
Responsibilities: Independently design, conduct, and interpret experiments that screen CAR constructs based on their function; Conduct hands-on laboratory work to evaluate Serotiny’s libraries in primary cells; Work collaboratively with other Laboratory team members on cell engineering, gene engineering, cell biology and molecular biology projects | 3/26/2022 |
| 7213 | Setpoint Medical Valencia, CA Associate Software Engineer BS in computer science or related Exp: 0+ years |
The SetPoint Medical Product Development team is seeking a motivated, hardworking, and intellectually curious junior engineer to work on a sophisticated active implantable device and connected software systems. Programming responsibilities may include, depending on the Software Engineer’s skillset, any part of the software development stack from low-level embedded code to high-level cloud development. The software engineer will work closely with senior engineers to receive training and mentorship. | 3/26/2022 |
| 7214 | Sherlock Biosciences Remote, Data Analyst BS in science, engineering, or computer science or related Exp: 1+ years |
We are seeking a Data Analyst Research Associate. As part of this role, you will support the market research team to build a comprehensive view of the competitive diagnostics landscape. Together with your supervisor, you will identify and evaluate public and proprietary information sources and develop solutions to pull, transform and store relevant structured and unstructured data. This will involve building and accessing data via APIs, parsing through text files, and building scalable data storage solutions. | 3/26/2022 |
| 7215 | Shoreline Biosciences San Diego, CA Research Associate/Sr. R.A. - Macrophage Biology BS or MS in immunology or related Exp: 0+ years |
Responsibilities: Differentiation and characterization of iPSC-Macrophages; Optimization of iPSC differentiation methods and techniques; Management of automated cell culture platforms for high throughput clone generation and characterization; Validation of observations from bioinformatic screens; Characterize iPSC-Macrophages using advanced flow cytometry techniques; Perform basic immunotherapy techniques (ELISA, flow, cytometry, microscopy, RT-PCR, and Western blot). | 3/28/2022 |
| 7216 | Shoreline Biosciences San Diego, CA Research Associate/Sr. R.A. - Cell Therapy BS or MS in immunology or related Exp: 0+ years |
Responsibilities: In vitro assay development for immunotherapy applications; Editing and engineering of tool cell lines for use in functional assays; Characterize immune cells using advanced flow cytometry techniques; High integrity culture of both target and effector cells; Perform basic immunotherapy techniques (ELISA, flow, cytometry, microscopy, RT-PCR, and Western blot). | 3/28/2022 |
| 7217 | Shoreline Biosciences San Diego, CA Research Associate/Sr. R.A. - Macrophage Cell Therapy BS or MS in immunology or related Exp: 0+ years |
Responsibilities: Genetic engineering or modulation of iPSC and Macrophages using virus, synthetic oligos and CRISPR-based methods; Characterize iPSC-Macrophages using advanced flow cytometry techniques; Design and management of external bioinformatic experiments; Culture and differentiation of engineered iPSC int; Design and manage automated cell culture systems; Perform basic immunotherapy techniques (ELISA, flow, cytometry, microscopy, RT-PCR, and Western blot). | 3/28/2022 |
| 7218 | Shoreline Biosciences San Diego, CA Research Associate/Sr. R.A. - Molecular Immunology BS or MS in immunology or related Exp: 0+ years |
Responsibilities: Implementation of classical and modern molecular biology techniques; Design and evaluation of CAR or synthetic antibodies; Generation of lentivirus and retrovirus systems for cell engineering; Cell engineering using mRNA. High integrity culture of both target and effector cells; Perform basic immunotherapy techniques (ELISA, flow, cytometry, microscopy, RT-PCR, and Western blot)Responsibilities: Implementation of classical and modern molecular biology techniques; Design and evaluation of CAR or synthetic antibodies; Generation of lentivirus and retrovirus systems for cell engineering; Cell engineering using mRNA. High integrity culture of both target and effector cells; Perform basic immunotherapy techniques (ELISA, flow, cytometry, microscopy, RT-PCR, and Western blot)Responsibilities: Implementation of classical and modern molecular biology techniques; Design and evaluation of CAR or synthetic antibodies; Generation of lentivirus and retrovirus systems for cell engineering; Cell engineering using mRNA. High integrity culture of both target and effector cells; Perform basic immunotherapy techniques (ELISA, flow, cytometry, microscopy, RT-PCR, and Western blot) | 3/28/2022 |
| 7219 | Shoreline Biosciences San Diego, CA Research Associate/Sr. R.A. - Synthetic Biology BS or MS in immunology or related Exp: 0+ years |
Responsibilities: Genetic engineering/modulation of iPSC and macrophages using virus, synthetic oligo and CRISPR-based methods; Sorting and expansion of engineered iPSC; Design and development of novel strategies to control macrophage biology; Protein engineering to improve macrophage performance; Perform basic immunotherapy techniques (ELISA, flow, cytometry, microscopy, RT-PCR, and Western blot) | 3/28/2022 |
| 7220 | Shoreline Biosciences San Diego, CA Process Development Associate II MS in life sciences or related Exp: 1+ years |
Responsibilities: Execute SOPs and protocols to support harvesting, concentration, cell product cryopreservation, and vialing; Maintain detailed experimental records, analyze, and interpret data, author SOPs, write reports and make presentations; Perform all functions to support process development activities leading up to and including cryopreservation of cell product; Order and maintain stocks of lab reagents and samples | 3/28/2022 |
| 7221 | Simbiosys Chicago, IL Clinical Data Abstractor BS in Life Sciences, Statistics, Biology, Computational Biology, Biomedical Engineering, Bioinformatics, or related Exp: 0-3 years |
You will be responsible for reviewing clinical radiology and pathology records, structuring and manipulating data, and helping to ensure that SimBioSys researchers have access to the appropriate data to perform their cutting-edge analyses. | 3/28/2022 |
| 7222 | Simbiosys Chicago, IL Clinical Trial Analyst MS in Life Science, Computer Science, Statistics, or related Exp: 0-2 years |
What you'll do: Extract, organize, and analyze clinical data to generate inputs for biophysical modeling engine; Perform imaging and clinical analysis for quality control assessment; Utilize SimBioSys software infrastructure to perform validation studies, virtual trials, sensitivity analysis; Perform statistical analysis in support of scientific publications. | 3/28/2022 |
| 7223 | Sinclair Research Auxvasse, MO Formulations Technician BS in Chemistry, Biochemistry, or related Exp: 0 years |
As a Formulations Technician, your day will consist of preparing dose formulation and other study related materials in compliance with study protocol and relevant regulations including GLP. Additionally, you will be responsible for the receiving and management of test articles and other common chemicals. As a member of the formulations team, you will monitor laboratory supplies and cleanliness to provide a clean and regulatory compliant laboratory. | 3/28/2022 |
| 7224 | Singota Bloomington, IN Quality Associate I - Batch Release BS in science Exp: 1-3 years |
The Quality Associate 1- Batch Release is responsible for managing the workflow of records for Manufacturing and QC/Development activities in accordance with company, client and regulatory quality standards, including the appropriate disposition of materials or manufactured product. This position is responsible for reviewing records for accuracy and completeness and for identifying discrepancies or issues that could result in product impact.The Quality Associate 1- Batch Release is responsible for managing the workflow of records for Manufacturing and QC/Development activities in accordance with company, client and regulatory quality standards, including the appropriate disposition of materials or manufactured product. This position is responsible for reviewing records for accuracy and completeness and for identifying discrepancies or issues that could result in product impact. | 3/28/2022 |
| 7225 | Singota Bloomington, IN Quality Associate I - Compliance BS in science Exp: 1-3 years |
The Quality Associate 1- Compliance will be responsible for general support and maintenance of the quality systems for adherence to regulatory requirements. The primary duties for the role include review and approval of deviations and CAPAs. This role will also assist with the change control program, and support auditing and inspection activities. This position also must positively interface with internal key stakeholders, clients and regulatory agencies regarding company quality and regulatory business. | 3/28/2022 |
| 7226 | MicroVention Aliso Viejo, CA Engineer I, R&D BS in mechanical, industrial, or materials science engineering Exp: 1 year |
Supports development of medical device products with work including writing or verifying specifications, designing new products, fixtures, test processes, equipment and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Largely self-directed, capable of meeting project goals with moderate supervision. | 3/30/2022 |
| 7227 | MicroVention Aliso Viejo, CA Engineer I, R&D BS in engineering or science Exp: 6 months |
Support development of medical device products with work including writing or verifying specifications; designing new products and fixtures; testing processes and equipment; and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Partially self-directed and capable of meeting project goals with supervision. | 3/30/2022 |
| 7228 | Akorn Amityville, NY Chemist I - 2nd Shift BS in chemistry or related Exp: 1 year |
During the 2nd shift, the individual will be responsible for providing analytical support to the department of Quality Control. The individual will be responsible to follow established procedures and protocols to conduct various independent and team driven laboratory experiments. The candidate should assist with the day-to-day maintenance of an orderly QC laboratory such as safety, ordering and receipt of reagents, Instrument calibration. | 3/30/2022 |
| 7229 | Akorn Somerset, NJ Microbiologist II - 2nd Shift BS in science, preferably microbiology Exp: 1 year |
Performs routine microbiological testing of products, raw materials, components and controlled environments according to site Standard Operating Procedures and compendial methods. Responsibilities include: Sterility Testing by Membrane Filtration and Direct Inoculation; Bioburden Testing by Membrane Filtration and Pour Plate Method; Antimicrobial Effectiveness Testing; Bacterial Endotoxin Testing | 3/30/2022 |
| 7230 | Sorrento Therapeutics San Diego, CA Process Development & Manufacturing Associate I BS in Chemical Engineering, Chemistry, Cell Biology, Microbiology, Molecular Biology, Biochemistry, or related Exp: 0+ years |
The process development and manufacturing associate I supports the oncolytic immunotherapy program at Sorrento. This role is responsible for the manufacture of clinical materials in compliance with current Good Manufacturing Practice (cGMP) and industry best practices. | 3/30/2022 |
| 7231 | Sorrento Therapeutics San Diego, CA QC Microbiology Associate BS in Microbiology or related Exp: 1-2 years |
Provide microbiological support and testing of cGMP environments as well as contributing to WFI testing, bioburden and sterility testing. | 3/30/2022 |
| 7232 | Sorrento Therapeutics San Diego, CA Research Assistant/Associate MS in Biology, Immunology, Biochemistry, or related Exp: 0+ years |
The successful candidate will play a role in in vivo studies testing therapeutic compounds in animal models and ex vivo immune cell analyses and/or PK/PD biomarker analyses. Responsibilities include: Conduct pre-clinical PK, PD, and efficacy studies; Execute in vitro/ex vivo assays such as flow cytometry, ELISA, and etc.; Acquire/analyze/summarize data and report data and troubleshoot for problems in experiments. | 3/30/2022 |
| 7233 | Sorrento Therapeutics San Diego, CA Research Associate (2) BS in Life Sciences or related Exp: 0+ years |
Our Upstream Antibody Process Development & Manufacturing team is currently looking for a Research Associate to help with the team to optimize antibody production. Major tasks include cell culture, cell line development, cell banking, benchtop bioreactor operation, troubleshooting and optimization of antibody production conditions. There are also many opportunities for this position to be involved in the cleanroom current Good Manufacturing Practice (cGMP) antibody production processes. | 3/30/2022 |
| 7234 | Sorrento Therapeutics San Diego, CA Research Associate – In Vitro Biology – Antibody Drug Conjugates BS or MS in Life Sciences or related Exp: 0-5 years |
Seeking an experienced Research Associate who will design, implement, and execute scientific research and development studies in collaboration with a larger research team. This individual will investigate the activity and specificity of ADCs towards a variety of targets in different indications. | 3/30/2022 |
| 7235 | Sorrento Therapeutics San Diego, CA Research Associate BS in Cell Biology, Molecular Biology, or related Exp: 0+ years |
Responsible for the development and implementation of in vitro functional T cell assays to support pre-clinical validation of CAR-T cellular therapies against cancer. The research associate has knowledge and hands on experience in molecular cloning, cell culture, and flow cytometry. | 3/30/2022 |
| 7236 | Sorrento Therapeutics San Diego, CA Senior Research Associate / Research Associate BS or MS in Biology, Chemistry, Biochemistry, or related Exp: 1-3 years |
Seeking an experienced Research Associate/Sr. Research Associate who will contribute to the general operations and testing for Quality Control. This position supports in-process, drug substance, drug product, and stability testing programs. Works independently under general supervision while operating the following: HPLC, spectrophotometers, pH meter, osmometer, balances, icIEF, CE-SDS, HIAC, Endosafe etc. | 3/30/2022 |
| 7237 | Somalogic Boulder, CO Manufacturing Associate I BS in Life Sciences, Chemistry, or related Exp: 1+ years |
The Manufacturing Associate will be responsible for performing a wide variety of manufacturing activities. The Technician will prepare and formulate reagents, perform routine maintenance and troubleshooting on laboratory equipment, and prepare kits for internal and external distribution. #578169 | 4/1/2022 |
| 7238 | Somalogic Boulder, CO Research Associate I (Technology Research) BS or MS in Molecular Biology, Biochemistry, Chemistry, or related Exp: 1-2 years |
The Technology Research team is seeking a Research Associate to assist in the identification and characterization of SOMAmer® protein detection reagents. This role will enable opportunities to learn laboratory techniques, high-throughput automation, data analysis, reagent inventory management, and other relevant skills at an established and rapidly growing company. #578834 | 4/1/2022 |
| 7239 | Somalogic Boulder, CO Research Associate I (Technology Research) MS in Molecular Biology, Biochemistry, Chemistry, or related Exp: 1+ years |
The Technology Research team is seeking a Research Associate to assist in the identification and characterization of SOMAmer® reagents. This position works in a fast-paced, team-oriented research group. The individual’s responsibilities will include generating new SOMAmer reagents using the SELEX process, performing protein affinity assays and preparing protein pulldown samples for LC-MS analysis. #577766 | 4/1/2022 |
| 7240 | Spark Therapeutics Philadelphia, PA HT Analytical Research Associate BS in engineering or life sciences Exp: 1+ years |
As a member of the HT assay team, the successful candidate will support routine testing of various analytical workflows – including associated activities such as reagent preparation, sample handling, data analysis, experiment documentation, and inventory management of lab reagents and consumables supplies – to support process and drug product development of gene therapy programs. | 4/1/2022 |
| 7241 | Spark Therapeutics Philadelphia, PA Drug Product Development Research Associate MS in pharmacy, biochemistry, biotechnology, biophysics, chemical engineering, biomedical engineering, or related Exp: 1+ years |
Responsibilities: Develop and use analytical methods to support experimentation and AAV characterization; Use experimental methods and techniques to support formulation development; Support colleagues by assisting in setup and experimentation using automation tools; Prepare presentations in various team and project meetings; Prepare process development reports and technical documents | 4/1/2022 |
| 7242 | SQZ Biotech Watertown, MA In-Vivo Associate BS or Associates in Animal Sciences, Veterinary Technology, Biology, or related Exp: 0.5-3 years |
Key Responsibilities: Animal husbandry duties such as daily cage checks, cage change, housing, and receipt of animal deliveries; Vivarium related maintenance including but not limited to, environmental monitoring, sanitation, pest monitoring, inventory and ordering of vivarium supplies, cage recycling and disposal program, and vivarium waste disposal; Daily cage checks and identification of abnormal animal conditions; Follow treatment plans and standardized treatments as prescribed by the veterinary designees; etc. | 4/1/2022 |
| 7243 | SQZ Biotech Watertown, MA Research Associate, Regenerative Medicine BS in science Exp: 1+ years |
The scope will encompass planning and execution of in vitro studies with a focus on transdifferentiation of somatic cells into neural cells. You will be part of a team identifying and testing cutting edge ideas with the goal of engineering and characterizing new cell therapeutics we can advance towards the clinic. Ongoing projects that you would contribute to have the potential to impact both neurodegenerative and neuroimmune disease indications. | 4/1/2022 |
| 7244 | Eurofins West Point, PA Downstream Process Development Scientist BS in biology, chemistry, or related Exp: 0-2 years |
Responsibilities: Perform lab-scale downstream processing of vaccine products and process intermediates; Perform assays on vaccine products, process intermediates, and related experimental samples using biochemical/analytical tests; Prepare solutions/reagents; Set-up process equipment for lab-scale experiments; Maintain records and experimental results following good manufacturing practices (GMP) | 3/21/2022 |
| 7245 | Pillar Biosciences Natick, MA Process Development Associate BS in biology, molecular biology, genetics, or related Exp: 1+ years |
Responsibilities: Characterization testing for raw materials, in process materials, and finished goods.; Complete documentation and analysis of test results.; Help to develop new test methods.; Support validation studies through execution of validation protocols. | 3/21/2022 |
| 7246 | Poseida Therapeutics San Diego, CA Quality Control Analyst BS in life sciences or related Exp: 1+ years |
The QC Microbiology Analyst I will be a member of a dynamic team that ensures the safety of our products at various points during the manufacturing process by performing facility monitoring, in-process and final product testing, and working cross-functionally with individuals and departments within the Pilot Plant Facility. | 3/21/2022 |
| 7247 | Poseida Therapeutics San Diego, CA Research Associate, In Vivo Gene Therapy MS in molecular biology, biology, or immunology Exp: 0 years |
This position offers an excellent opportunity to develop new gene editing and gene therapy products in an exciting and dynamic environment focused on cutting-edge gene editing and insertion technology for in vivo gene therapies. This role will focus on discovery-phase pharmacology assay development, with particular focus on techniques suitable for evaluating cells at the genomic and messenger levels. | 3/21/2022 |
| 7248 | Poseida Therapeutics San Diego, CA Manufacturing Associate BS in biology, chemistry, or engineering Exp: 0+ years |
The Manufacturing Associate is part of the Poseida internal manufacturing team in support of Poseida’s clinical production of cell therapies. This position will support front line non-viral cell therapy GMP production activities, process transfers, and technology improvements towards the successful delivery of released product to meet the needs of Poseida’s clinical trials. | 3/21/2022 |
| 7249 | Precigen Germantown, MD Research Associate, Autoimmunity BS or MS in immunology, molecular biology, or related Exp: 1 year |
Responsibilities include: Apply immunological laboratory techniques to research projects; Perform experiments with a careful attention to detail and accurately record procedures, data and results in electronic lab notebook (ELN); Analyze and present data to supervisor and/or group members and make intellectual and technical contributions to the team. | 3/21/2022 |
| 7250 | Prelude Therapeutics Wilmington, DE Research Associate, Cellular Asssays BS or MS in cell/molecular biology, or other life sciences Exp: 1-3 years |
The Research Associate will contribute to the company’s efforts to design and develop a pipeline of novel, orally bioavailable, small molecule therapies that target key drivers of cancer cell growth, survival, and drug resistance. The successful candidate will have a cell/molecular biology and informatics background and is able to work in a collaborative team environment, perform experiments, organizes, and analyzes results, and communicates effectively to support R & D teams. | 3/21/2022 |
| 7251 | Prominex San Diego, CA Research Associate I/II MS in science Exp: 0-2 years |
We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 3/21/2022 |
| 7252 | Protein Fluidics Burlingame, CA Research Associate BS in biology, biochemistry, bioengineering, or related Exp: 1+ years |
Responsibilities: Perform cell culture, cell maintenance, and banking; Help maintain reagents and lab supplies to support research projects; Conduct 2D and 3D cell based assays; Execute Pu·MA System testing protocols and automated assays; Help with processing and quality control of microfluidic flowchips and instruments; Maintain accurate documentation. Must have plate reader experience and hands-on experience with cell culture and cell-based assays. | 3/21/2022 |
| 7253 | Protein Metrics Cupertino, CA Software and Alogithm Engineer BS or MS in computer science, chemical engineering, biochemistry, or chemistry Exp: 1+ years |
We are seeking a talented software and algorithms engineer who is excited to join a well-funded, cash-flow positive, software start-up serving life science researchers. We expect the applicant to be able to work in our Cupertino, CA office and to contribute with our software team immediately. The candidate should have strong understanding of algorithms and produce clean professional code. | 3/21/2022 |
| 7254 | PTS Diagnostics Whitestown, IN Controls and Systems Engineer BS in electrical engineering or related Exp: 1-3 years |
Controls and Systems Engineer is responsible for assessing systems, determining problems, providing solutions to issues that arise, designing systems, upgrading systems, maintaining systems, and brainstorming possible improvements that can be made to PTS systems. Controls engineer is responsible for ensuring PTS create the best products possible in the most efficient manner. The position will be responsible for ensuring that all equipment is properly maintained. | 3/22/2022 |
| 7255 | Puretech Boston, MA Associate/Senior Associate Scientist BS or MS in chemistry, chemical engineering, materials science, pharmaceutical science, or related Exp: 0-3 years |
PureTech Health is seeking an associate scientist I/II with prior laboratory experience and a passion for making an impact. In this role, the candidate will support formulation development and characterization of our inflammation-targeting platform and drug candidates. The candidate will work closely with the research team to support current pipeline candidates as well as new project initiatives | 3/22/2022 |
| 7256 | Quadrant Biosciences Syracuse or Buffalo, NY Clinical Laboratory Technologist BS in medical technology or related Exp: 1+ years |
The Clinical Laboratory Technologist will perform tasks to serve a high throughput testing laboratory. Responsibilities include: Follow clinical laboratory testing procedures and policies in the performance of routine and specialized tests; Identify the source and nature of test problems and make appropriate recommendations; Apply scientific methods in problem solving and assist in evaluation of new methods and techniques | 3/22/2022 |
| 7257 | Quatapore South San Francisco, CA Research Associate BS or MS in physics, biochemistry, molecular biology, or related Exp: 1-3 years |
This position will play a key role in developing Quantapore’s sequencing technology and optimizing the associated procedures and protocols. The candidate will work closely with our experts in biochemistry, molecular biology, bioinformatics and engineering. This position is hands-on and requires operating in a fast-moving environment. | 3/22/2022 |
| 7258 | Quantimetrix Redondo Beach, CA Formulation Chemist BS in chemistry or related Exp: 1 year |
The Formulation Chemist prepares and intermediates and formulates products using approved documentation and SOPs in compliance with cGMP’s. Performs in-process testing of products prior to submission to QC. Interacts with QC/QA and other departments as required. | 3/22/2022 |
| 7259 | QurAlis Cambridge, MA Research Associate, Compound Management BS in science or engineering or related Exp: 1+ years |
QurAlis is seeking a highly motivated Research Associate to manage and support our compound management system. This position will work closely with the Lab Manager to learn the various systems in place for tracking and organizing the compounds that will be used in decision-making experiments. | 3/22/2022 |
| 7260 | Rakuten Medical San Diego, CA Research Associate I, Upstream BS or MS in life sciences, bioengineering, or related Exp: 1+ years |
Rakuten Medical is currently looking for a highly motivated individual to support cell line and upstream process development activities. This candidate will join Rakuten Medical ’s CMC team focusing on various aspects of preclinical antibody development including transfection and single cell cloning, cell culture process development, late-stage characterization, technology transfer and research material generation. | 3/22/2022 |
| 7261 | MacroGenics Rockville, MD Manufacturing Science & Technology Associate II MS in Biology, Chemistry, Biochemistry or a related life sciences or engineering field Exp: 0 years |
The Manufacturing Technology Associate II provides technical support to biopharmaceutical drug substance manufacturing operations for MacroGenics’ late-stage clinical and commercial programs. The position will work in partnership with Manufacturing Operations and BioPharmaceutical Development to support technology transfers, process and equipment validations, and routine manufacturing at internal sites. | 3/22/2022 |
| 7262 | MacroGenics Rockville, MD Animal Health Technician I BS in science Exp: 0 years |
The Animal Health Technician I is responsible for executing animal care duties and responsibilities that enable us to support rapid advancement of preclinical programs. | 3/22/2022 |
| 7263 | MacroGenics Rockville, MD QC Analyst I - Environmental Monitoring BS in science Exp: 0 years |
This position is responsible for performing activities in support of the microbiology and environmental monitoring testing programs including monitoring of the manufacturing cleanrooms. This individual will guide and partner with lower level QC analysts and provide ongoing feedback and information to the QC supervisors to ensure accurate documentation, timely completion of all EM and microbiological related testing, and timely review of data, while adhering to standard operating procedures and cGMPs. | 3/23/2022 |
| 7264 | MacroGenics Rockville, MD Manufacutring Associate II BS in science or engineering or related Exp: 1+ years |
The Manufacturing Associate II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 3/23/2022 |
| 7265 | Civio Radiotherapy Orange City, IA Design Engineer I - OEM Projects BS in engineering Exp: 1-3 years |
Responsibilities include: Design Engineering: Designs, develops and maintains products within and outside of existing product lines. Responsible for generation and approval of product development documentation on assigned projects. Shows introductory knowledge of the CAD system(s). Able to make decisions on simple technical matters related to product design. | 3/23/2022 |
| 7266 | SeaSpine Carlsbad, CA Design Engineer BS in engineering Exp: 1-2 years |
Create CAD models and detailed engineering drawings using Creo to modify/maintain existing spine implant products and support new device designs; Update and write documentation/design history files to support designs in accordance with Design Control and Risk Management procedures; Work with Engineering Services team to generate and analyze test data and reports to verify that prototypes meet functional and performance specifications; Collaborate with internal teams, design surgeons, and manufacturers to establish necessary design inputs, uphold project plans, and achieve project objectives | 3/23/2022 |
| 7267 | RegenexBio Rockville, MD Clinical Research Associate MS in science or engineering Exp: 1+ years |
You will support and coordinate the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs and acts as a pivotal point of contact for the clinical trial team. Under general supervision, you will assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. | 3/23/2022 |
| 7268 | RegenexBio Rockville, MD Associate Scientist, Upstream Operations, Vector Core BS in science Exp: 1 year |
The Vector Core department at REGENXBIO is currently in search of an Associate Scientist to join its Upstream Operations team! Vector Core at REGENXBIO plays a key role bridging the Research and Process Development groups by developing and utilizing high throughput methods for material generation, as well as working on exciting next generation AAV (adeno-associated virus). In this role, you will be responsible for producing non-GMP recombinant AAV vectors in support of pre-clinical and/or IND enabling studies. | 3/23/2022 |
| 7269 | RegenexBio Rockville, MD Associate Scientist, Bioanalytical Sciences (LCMS) MS in science Exp: 1+ years |
You will be responsible for developing and validating bioanalytical methods and testing bioanalytical samples to support our gene therapy product pipeline. You will have the exciting opportunity to work with the most cutting-edge technologies and a new Sciex 7500 Triplequad LCMS system in a brand-new lab. You will explore novel techniques/technologies and apply analytical stringency and savvy for the stage of development, and in alignment with regulatory expectations. | 3/23/2022 |
| 7270 | RegenexBio Rockville, MD Associate Scientist I, Analytical Development (Potency) BS in science Exp: 0 years |
As Associate Scientist, you will be trained to work from entry level up to conduct basic lab functions such as practicing aseptic technique, preparing cell culture media and other laboratory solutions, passaging and maintaining mammalian cell lines, assisting in the cleaning and maintenance of laboratory equipment, running experiments adhering to written instructions, and coordinating other basic lab activities. | 3/23/2022 |
| 7271 | RegenexBio Rockville, MD Associate Scientist, Bioanalytical (Molecular Biology) BS or MS in science Exp: 1-2 years |
You will be responsible for developing and validating bioanalytical methods to support our gene therapy products pipeline. You will have the opportunity to collaborate with many different groups across the organization, including Research and Early Development, Quality, and Clinical Development and may oversee Contract Research Organizations to ensure that all applicable bioanalytical test methods are appropriate for the stage of non-clinical and/or clinical development. | 3/23/2022 |
| 7272 | Replimune Framingham, MA Manufacturing Associate BS in science or engineering or related Exp: 1-3 years |
The Manufacturing Associate is responsible for executing the cGMP manufacturing operations to support the production of Replimune products at the Framingham, MA, facility. This individual will collaborate with multiple departments to support the manufacturing technology transfer and startup of the production facility and will assist with the generation/revision of Standard Operating Procedures and associated documentation to ensure manufacturing readiness. | 3/23/2022 |
| 7273 | ResearchDx Irvine, CA Clinical Laboratory Scientist BS in clinical laboratory sciences, life sciences, or physical sciences Exp: 0-2 years |
The CLS is responsible for performing routine to specialized molecular technologies, flow testing, quality control, and daily operation. The CLS works closely with supervisors and the laboratory director to ensure good quality and proper Turn Around Time (TAT) for the test results. | 3/23/2022 |
| 7274 | ResearchDx Irvine, CA Laboratory Associate BS in health or biological sciences Exp: 0 years |
Seeking a motivated and detail-oriented individual to work in a fast-paced clinical research laboratory. This is an entry-level position that is great for someone looking to get their “foot in the door” in a clinical laboratory setting. You will work both independently and in team-oriented capacities. The ideal candidate will have a good attitude, especially when working flexible or long hours due to special projects. | 3/23/2022 |
| 7275 | ResearchDx Irvine, CA Research Associate BS or MS in science Exp: 1-2 years |
The Research Associate will conduct routine to complex experimental procedures within the overall scope of a research project and/or diagnostic test development project. Maintains all appropriate records regarding data collection and interpretation of results. Familiar with basic molecular biology concepts, practices, and procedures including cell culture, PCR, RT-PCR, sequencing, nucleic acid extraction, ELISA, and use of fluorescence-based nucleic acid detection techniques. | 3/23/2022 |
| 7276 | Resilience Waltham, MA Research Associate, Molecular Assays, Cell Therapy BS or MS in molecular biology, virology, cell biology, immunology, pharmaceutical sciences, or related Exp: 0-2 years |
This team plays a key role in understanding and optimizing cell processes and cell product attributes that correlate to patient outcomes, designing genomic, transcriptomic, protein, cytokine, and other assays. The Research Associate will support the development of molecular assays with a focus on qPCR and/or digital droplet PCR (ddPCR) and provide support in Next-Generation Sequencing (NGS), transcriptomics assays, and/or bioinformatics as required. | 3/23/2022 |
| 7277 | Resilience Waltham, MA Research Associate II, Process Development BS or MS in cell biology, immunology or related Exp: 1+ years |
Resilience is seeking a talented Research Associate II to join us as a valued member of the Cyto Innovation Process Development team. This researcher will focus on hands-on execution of protocols involving induced pluripotent stem cells (iPSCs) for Resilience’s developing Regenerative Medicine Modality. The successful candidate will support the development of Resilience’s best-in-class hypoimmune iPSC generation platform and will collaborate broadly with colleagues in platform R&D, analytical development, and other teams across the Resilience biomanufacturing network. | 3/23/2022 |
| 7278 | Resilience Waltham, MA Senior Research Associate, Analytical Devleopment MS in analytical chemistry, biochemistry, molecular/cellular biology or related Exp: 1+ years |
Resilience is seeking a talented Senior Research Associate to contribute to the Gene Therapy Analytical Development group with a focus on cell and molecular analytical development. This researcher will help establish Resilience as a leader in gene therapy analytical science through the development and application of best-in-class testing strategies, working in collaboration with analytical groups across the Resilience network. | 3/23/2022 |
| 7279 | Resilience East Norriton, PA Senior Research Associate, Vector Devleopment BS or MS in bioengineering, biology, virology, or related Exp: 1+ years |
This team supports preclinical and clinical pipelines enabling IND filings for Resilience's partners and drives development and implementation of innovative internal technology platforms. The Senior Research Associate will play a significant role in the development and optimization of Resilience’s lentiviral vector manufacturing processes, focusing on both upstream and downstream process unit operations. This researcher will be a key member of a team establishing scalability across experimental and clinical supply processes and will support technology transfer to Resilience's in-house GMP manufacturing facility. | 3/23/2022 |
| 7280 | Resilience Mississauga, ON Research Associate I - Upstream BS or MS in science Exp: 0+ years |
The incumbent will produce and characterize protein products in cell culture. Develop and scale-up protein production processes. Plan and carry out integrated experimental projects to complete drug development program and project objectives. Support bioanalytical characterization. Prepare documents and reports to support non-GMP and GMP manufacturing activities and regulatory submissions. Participate in early phase GMP manufacturing and related activities. | 3/23/2022 |
| 7281 | Resilience Alachua, FL Biomanufacturing Associate I BS in microbiology, biology, or chemistry Exp: 0-1 years |
This position will assist in production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). Assist with upstream related activities including cell culture at small and large scale, cell transfection, media and buffer preparation, and bioreactor and fermenter-based production. Assist with downstream related activities including chromatography purification, centrifugation and ultracentrifugation, ultrafiltration/ diafiltration, and viral clearance. | 3/23/2022 |
| 7282 | Resilience East Norriton, PA Manufacturing Technician II - Cell Therapy BS in science Exp: 1-3 years |
The Technician II, Cell Therapy Manufacturing position is responsible for the hands-on clinical manufacturing of cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development and report to the Bioprocess and Cell Therapy Supervisor. | 3/23/2022 |
| 7283 | Rocket Pharma Cranbury, NJ Quality Control Associate Scientist BS in biology, virology, molecular biology, or related Exp: 0-2 years |
We are seeking a Quality Control Associate Scientist with the responsibility to support clinical manufacturing of a range of Gene Therapy products. Technical proficiency in analytical methodology for drug substances and drug products is required for gene based products. | 3/24/2022 |
| 7284 | Nitrosome Biosciences Dallas, TX Research Associate – Discovery Biology B.S./B.A. in biological sciences Exp: 0-2 years |
As part of Nitrase Tx’s growth and goal of advancing a pipeline of Nitrase focused targets and drugs, we are seeking to recruit a Research Associate – Discovery Biology. This entry-level position requires enthusiasm and a strong work ethic, the ability to learn new biology and methods quickly, and to problem-solve creatively. The Research Associate will learn to develop new assays to measure the activity and characteristics of new enzymes as they are discovered, and to help develop and conduct biomarker assays in various tissues. The successful candidate will work collaboratively in a cross-functional environment and learn the many steps involved in drug discovery and development. | 3/23/2022 |
| 7285 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 3/23/2022 |
| 7286 | Sigilon Therapeutics Cambridge, MA Assistant/Associate Engineer, Cell Processing Development B.S. in Biomedical Engineering, Biology, or Biochemistry or relevant discipline Exp: 0-2 years |
Sigilon Therapeutics is looking for an experienced process development scientist to join the team responsible for enhancing and evolving the manufacturing process for Sigilon’s encapsulated allogeneic cell therapy platform. Key objectives will be to maintain the production of our cell therapy bioprocess, develop robust and scalable cell therapy bioprocesses, and transfer these processes to contract manufacturing partners. | 3/23/2022 |
| 7287 | Sigilon Therapeutics Cambridge, MA Assistant/Associate Scientist, Biomaterials Process Development Sc. or M.Sc. degree with a focus on Biomaterials, Engineering, Biochemistry, Biology, or relevant discipline Exp: 0-2 years |
Sigilon Therapeutics is looking for a new or experienced process development scientist to join the team responsible for optimizing the manufacturing process for Sigilon’s encapsulated allogeneic cell therapy platform. Key responsibilities will include maintaining the production of our cell therapy bioprocess, helping develop improvements to the current manufacturing process, and exploring innovations to improve scalability. | 3/23/2022 |
| 7288 | Sigilon Therapeutics Cambridge, MA Associate Scientist, Chemistry B.S degree in Chemistry, Polymer Chemistry, Biochemistry or other relevant discipline Exp: 0-2 years |
Sigilon Therapeutics is seeking an Associate Scientist in Chemistry to join the Process Development team, focused on enhancing and evolving the manufacturing process for Sigilon’s encapsulated allogeneic cell therapy platform. The Associate Scientist is responsible for developing robust and scalable processes for the synthesis of organic compounds and polymer conjugates. Works within the Process Development organization as well as cross functionally with peers to advance programs into the clinic. Excellent communication skills and ability to work in a highly interactive and matrixed environment. | 3/23/2022 |
| 7289 | Alivio Therapeutics [Puretech] Boston, MA Associate/Senior Associate Scientist BS or MS in Chemistry, Chemical Engineering, Materials Science, Pharmaceutical Science, or related discipline Exp: 0-3 years |
PureTech Health is seeking an associate scientist I/II with prior laboratory experience and a passion for making an impact. In this role, the candidate will support formulation development and characterization of our inflammation-targeting platform and drug candidates. The candidate will work closely with the research team to support current pipeline candidates as well as new project initiatives | 3/23/2022 |
| 7290 | Nitto Denko Avecia Milford, MA Research Scientist-Level TBD (2162) RS I- MS Exp: 1+ year |
Nitto Avecia Research Scientist are responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides.We currently have openings at all levels! | 3/24/2022 |
| 7291 | Avidity Biosciences San Diego, CA RESEARCH ASSOCIATE/ SR RESEARCH ASSOCIATE IN ANALYTICS AND FORMULATIONS Bachelor’s degree in chemistry, biology, or pharmaceutical sciences Exp: 0-3 years |
We are seeking a Research Associate/ Sr Research Associate in Analytics and Formulations. This individual will develop and run analytical assays. They will also screen formulations and conduct stability studies. The Research Associate/Sr Research Associate will report to Scientist, Analytics and Formulations. | 3/24/2022 |
| 7292 | Biomarker Strategies Rockville, MD Technician or Research Assistant (Part-time positions considered) BS Exp: 1+ years |
assist in the development of a commercialization-focused cancer diagnostic system. Candidates will be responsible for performing research and development experiments, and to be able to summarize experiments and results. This position is a wet lab position and candidate will predominately perform work at the bench. | 3/24/2022 |
| 7293 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: one year |
development of a commercialization-focused cancer diagnostic system. Candidates will be | 3/24/2022 |
| 7294 | CRISPR Therapeutics Cambridge, MA Research Associate/Research Associate II, Analytical Development RA: BS; RA II: MS Exp: RA: 0-3 years; RA II: 0-3 years |
responsible for performing research and development experiments, and to be able to | 3/25/2022 |
| 7295 | CRISPR Therapeutics Cambridge, MA Research Associate II, Editing Technologies MS degree in Molecular Biology, Cell Biology, Biochemistry or a related discipline Exp: 1+ year |
summarize experiments and results. This position is a wet lab position and candidate will | 3/25/2022 |
| 7296 | CRISPR Therapeutics Cambridge, MA Research Associate II, Protein Science MS degree in biology, biotechnology, biochemistry, bioengineering, chemistry or related discipline Exp: 1+ years |
predominately perform work at the bench | 3/25/2022 |
| 7297 | CRISPR Therapeutics Cambridge, MA Research Associate I, Oligonucleotide Purification, Non-Viral Delivery MS degree in Chemistry, Chemical Engineering, Biochemistry, Bioengineering or related field Exp: 1+ years |
We are seeking a highly motivated Research Associate to join our Non-viral Delivery team and help expand our capabilities in the production of therapeutic oligonucleotides. The successful candidate will apply their knowledge of chromatographic separation techniques to the purification of chemically synthesized deoxyoligonucleotides and guide RNAs. This position with support cross-functional efforts in multiple therapeutic areas (Hematology, Immuno-oncology, and Regenerative Medicine) as well as the development of our non-viral delivery platform. | 3/25/2022 |
| 7298 | CRISPR Therapeutics Cambridge, MA Research Associate II, Oligonucleotide Synthesis, Non-viral Delivery MS degree in Chemistry, Chemical Engineering, Biochemistry, Bioengineering or related field Exp: 1+ years |
CRISPR Therapeutics is seeking a highly motivated Research Associate to join our Non-viral Delivery team in Cambridge, Massachusetts. The incumbent will be responsible for the synthesis and analysis of oligonucleotides to support the generation of guide RNAs with novel chemistries. This position will support therapeutic programs in multiple disease areas and will contribute to the development of a novel nucleic acid conjugation platform. Prior experience in oligonucleotide synthesis and characterization is desired. | 3/25/2022 |
| 7299 | For Doz Parma [Ferndale Pharma Group] Ferndale, MI Chemist Bachelor of Science in Chemistry or a closely related field Exp: one to two years |
Carry out routine day-to-day quality control testing of Water, Raw Materials, Bulk, Finished Products and Stability samples in the Quality Control Laboratory. Perform routine chemical testing by such means as HPLC, GC, FTIR, UV Spectrophotometry, Titrations and other physical and chemical techniques. Review note books and generate test data reports. Write and revise SOPs. Prepare protocols, perform testing for special investigations and write scientific reports. | 3/25/2022 |
| 7300 | GenEdit South San Francisco, CA Research Associate/Sr. Research Associate, Chemistry, Platform Program Bachelor or Master’s in Chemistry, Biochemistry, Chemical Biology, Chemical Engineering, Biomedical Engineering, or Material Science & Engineering Exp: RA: 0-2 years |
GenEdit is seeking a highly self-motivated and goal-oriented Research Associate/SRA with experience in organic synthesis of bio-synthetic polymer and/or complex organic molecule characterization to join our team. This position will also require experience in polymer and/or macromolecule characterization utilizing various separation and detection techniques in support of research, regulatory and business efforts. This full-time position will report to the Sr. Scientist in Chemistry and will be responsible for synthesis of novel polymer molecules, assist with developing, implementing, and validating analytical methods to characterize novel polymers for gene delivery nanoparticles. This position will also participate in the development and routine performance of polymer characterization assays for identity and purity, preparation of certificates of analysis (COA), and preparation of standard operating procedure (SOP). Additional duties and responsibilities may be required as needed. The successful candidate will be a highly collaborative, resourceful, and an effective team-player who is enthusiastic about tackling challenging complex scientific and technical problems with novel approaches and solutions. | 3/25/2022 |
| 7301 | Invivotek [Genesis Biotechnology Group] Sunnyvale, CA Biochemist Assistant - CBI BS degree in a scientific field; or diploma in Medical Technology or Histology Exp: 0-5 years |
The Biochemist Assistant will possess the technical expertise to function effectively in a GLP toxicology and drug development environment. Skills in specialized techniques in IHC, carrying-out immunostaining protocols and methods. Provides support to other areas of CBI as qualified by training and/or experience. | 3/25/2022 |
| 7302 | Invivotek [Genesis Biotechnology Group] Hamilton, NJ Research Associate I Bachelor of Science degree in Life Sciences Exp: 1 to 2 years |
We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 3/25/2022 |
| 7303 | Myriad Genetics South San Francisco, CA Research Associate I BS or MS in molecular biology, biochemistry, or related Exp: 1+ years |
What You'll Do: Method Research: invent assay methodologies that will enable expansion into new target markets; Assay Development: develop new assay chemistries with the goal of minimizing cost and turnaround time while maintaining accuracy; Sequencing Protocol Design: design panels for the latest sequence capture methods and optimize protocols for targeted clinical sequencing assays What You'll Do: Method Research: invent assay methodologies that will enable expansion into new target markets; Assay Development: develop new assay chemistries with the goal of minimizing cost and turnaround time while maintaining accuracy | 3/10/2022 |
| 7304 | Myriad Genetics Salt Lake City, UT Laboratory Technician BS or MS in chemical, physical, biological, or medicinal sciences Exp: 0+ years |
Responsibilities: Complying with the laboratory’s technical, administrative and safety policies and procedures; Participating in the laboratory’s quality assurance plan, adhering to quality control and preventive maintenance policies and appropriately documenting these activities; Working as part of a team to produce repeatable quality results; Maintaining a clean and organized laboratory space; Following Standard Operating Procedures (SOPs); Operating high performance liquid handling robots. Multiple levels available based on experience/education | 3/10/2022 |
| 7305 | Mythic Therapeutics Waltham, MA Associate Scientist/Sr. Associate Scientist, Antibody Engineering BS or MS in Biology, Molecular Biology, Biochemistry, or related Exp: 0-5+ years |
As a member of a project team, you will focus on early discovery and engineering of therapeutic antibodies and execute biophysical assays for characterization of antibody drug candidates. | 3/13/2022 |
| 7306 | Mythic Therapeutics Waltham, MA Associate Scientist I/II, Protein Production BS or MS in life sciences or related Exp: 1-4 years |
In this role, you will support the early development of therapeutic antibodies and have an opportunity to contribute to multiple high priority projects. The ideal candidate will have experience in antibody expression and purification as well as a background in molecular biology, chemical engineering, protein biochemistry or a related field. | 3/13/2022 |
| 7307 | Nanomix Emeryville , CA Research Associate BS in Chemistry, Chemical Engineering, Biology, or Biological Engineering Exp: 3+ months |
Design and develop new cartridge prototypes, working with biosensors, filters, conjugate pads, microfluidics, device programming, etc. to enable specific biological assays on the eLab platform. Design processes required to manufacture product components by developing fixtures, installing necessary components on machinery, scripting robotic liquid handlers, drafting qualification requirements, and writing quality documentations. Design and execute biological wet lab experiments. | 3/13/2022 |
| 7308 | NanoCellect San Diego, CA Research Technician BS in engineering Exp: 0 years |
Responsibilities: Perform a visual inspection of disposable cartridges and other consumables; Manually assemble cartridges for the purpose of testing; Carefully follow experiment procedures step-by-step; Be able to understand & develop an intuition for the underlying reasons and principles behind the procedures; Look for patterns of behavior in test results, and seek improvements. | 3/13/2022 |
| 7309 | Neumora Cambridge, MA Research Associate - Animal Care BS or MS in neuroscience, psychology, biology, or related Exp: 1-3 years |
The successful candidate will perform hands-on research studies designed to investigate novel targets and mechanisms in neuropsychiatric and neurodegenerative disorders. The ideal applicant has experience in stereotaxic small animal surgery, gas anesthesia techniques, and commits attention to detail and research excellence. The individual will work on complex and exciting projects and will serve an important role that interfaces with scientists across the Discovery teams. | 3/13/2022 |
| 7310 | Neuron23 South San Francisco, CA Research Associate, DMPK BS or MS in Chemistry, Biology, Pharmacology, Pharmaceutical Sciences, Biochemistry, or related Exp: 0-10 years |
We seek an experienced and highly motivated Research Associate/Senior Research Associate to work within the DMPK group to conduct absorption, distribution, metabolism, excretion (ADME) studies to support the discovery and development of drug candidates. Coordinate and track external DMPK studies at various CRO. | 3/13/2022 |
| 7311 | Nexelis Laval, QC R&D Associate Scientist II, Bacteriology BS in chemistry, biochmistry, immunology, or related Exp: 0+ years |
The Associate Scientist is responsible for laboratory work and documentation based on their assignment within the laboratory. They ensure that analyses and assigned tasks are performed in accordance with appropriate SOPs. | 3/13/2022 |
| 7312 | Noble Life Sciences Woodbine, MD Animal Lab Tech BS in sciences Exp: 1+ years |
Responsibilities include: Perform duties in accordance with relevant study protocols and the Standard Operating Procedures (SOPs); Follow and perform standard operating procedures (SOP) & Protocols on study and stock animals; Administer test and control articles or other substances (i.e. medications) to animals by various routes of administration; Collect blood samples from animals through various methods, process blood samples and collect bone marrow samples. | 3/13/2022 |
| 7313 | Noble Life Sciences Woodbine, MD Animal Care Tech BS in sciences Exp: 1+ years |
Responsibilities Include: Read, understand and follow all SOP’s, Quality Assurance Standards and perform duties in accordance with the study protocol; Monitor daily animal health and wellness checks and report any abnormal animal conditions to the supervisor and/or the Study Director and record observations in appropriate logs; Ensure that all animals are fed the proper diet and have adequate water within the date and time requirements; Clean and disinfect animal holding rooms daily. | 3/13/2022 |
| 7314 | Noble Life Sciences Woodbine, MD Study Coordinator BS in sciences Exp: 1+ years |
Responsibilities include but are not limited to: Assist Study Director in determining staffing requirements, scheduling and documenting all critical events; Assist Study Director with protocols and reports preparation; Maintain inventory levels specified by the protocol and/or SOP; Prepare all data forms required to conduct the study as specified by the protocol and/or SOP; Process, document, store and ship specimens according to Study Protocol | 3/13/2022 |
| 7315 | Nushores Bioscience Little Rock, AR Quality and Regulatory Manager BS in sciences or related Exp: 1+ years |
Will work closely with C-level management, research scientists, manufacturing, and our Quality and Regulatory services providers to move NuShores’ product development efforts from our pipeline of licenses and internally developed innovations and inventions to achieve strategic and tactical business goals. The Quality and Regulatory Manager owns, audits, and drives improvements within the NuShores (CMP) Quality Management System (QMS). He / She also manages NuShores’ registrations, applications, readiness to enter new markets. | 3/13/2022 |
| 7316 | Oakwood Labs Solon, OH Quality Control Chemist BS in Chemistry, Biochemistry, Biology, or related Exp: 1-4 years |
Responsibilities include: Perform stability studies; Perform raw material, in-process product, and final product release testing; Assess data to determine if the material tested meets specifications; Participate in investigational testing and write reports; Execute mathematical calculations as outlined in test methods | 3/13/2022 |
| 7317 | Oakwood Labs Oakwood Village, OH Chemist, Entry Level BS in Chemistry, Biology, or related Exp: 0 years |
You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentationThere will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, etc. | 3/13/2022 |
| 7318 | Oakwood Labs Oakwood Village, OH Biomedical Engineer / Chemical Engineer BS or MS in Chemical Engineering, Chemistry, or related Exp: 0-1 years |
Responsibilities include: Perform pre-formulation laboratory experiments and studies; Perform process scale-up from laboratory to pilot laboratory; Perform process scale-up from pilot laboratory to manufacturing facility; Work on technology transfer activities | 3/13/2022 |
| 7319 | Ocugen Malvern, PA Research Associate MS in Pharmaceutical Science, Chemistry, Biochemistry, Biology, or related Exp: 1 year |
This role will be responsible for routine analytical sample testing and data analysis to support biologics and gene therapy programs at Ocugen. The successful candidate will participate in process and analytical assay development and validation activities. Candidate is expected to work with the discovery and R&D group to support cell-based potency assays. Perform technical and laboratory activities focused on Cell and Gene therapy and Vaccine process development activities in the R&D and process development labs. | 3/13/2022 |
| 7320 | Ocugen Malvern, PA Research Associate, Analytical Development MS in Pharmaceutical Science, Chemistry, Biochemistry, Biology, or related Exp: 1 year |
This role will be responsible for routine analytical sample testing and data analysis to support biologics and gene therapy programs at Ocugen. The successful candidate will participate in process and analytical assay development and validation activities. Candidate is expected to work with the discovery and R&D group to support cell-based potency assays. Perform technical and laboratory activities focused on method development and qualification for biological programs. | 3/13/2022 |
| 7321 | Onchilles Pharma San Diego, CA Research Associate - Protein Engineering & Drug Development BS or MS in Cellular Biology, Molecular Biology, Biochemistry, or related Exp: 1-2 years |
Responsibilities: Driving therapeutic innovation and directly contributing to the Onchilles pipeline; Integral member of a highly collaborative team executing on time-sensitive protein engineering projects all the way from protein expression design & generation through protein purification and characterization; Maintaining mammalian cell culture lines; Independently evaluate and trouble-shoot experiments in a timely manner | 3/13/2022 |
| 7322 | Onchilles Pharma San Diego, CA Research Associate - Preclinical Research & Cancer Biology BS or MS in Cellular Biology, Molecular Biology, Biochemistry, or related Exp: 1-2 years |
Responsibilities: Coordinate with Scientific teams to achieve company objectives, specificallythrough the execution of experimental designs with limited supervision and self-driven; Conduct novel investigations into biochemical pathways as they apply to drugdevelopment; Perform sample preparation and analysis with ex vivo tissues for assays(histology, protein, RNA, and DNA analysis); Contribute to the adaptation of existing assays and development of novel assaysthat comply with standards required of preclinical in vivo studies | 3/13/2022 |
| 7323 | OncoResponse Seattle, WA Research Associate - Cellular and Molecular Biology BS in Cellular Biology, Molecular Biology, or related Exp: 1+ years |
OncoResponse seeks a Research Associate to support our efforts to develop antibody-based immunotherapeutics to treat cancer. In this role you will utilize a wide range of experimental techniques to support our efforts to develop antibody-based therapies. The position requires strong foundational knowledge of cellular and molecular biology, the ability to work on multiple projects simultaneously, and the enthusiasm to tackle new experimental techniques. | 3/13/2022 |
| 7324 | OncoResponse Seattle, WA Senior Research Associate/Associate Scientist – Protein Chemistry BS in Biochemistry and Related Exp: 1 year |
OncoResponse seeks a Research Associate/Associate Scientist to support our efforts in developing antibody-based immunotherapeutics to treat cancer. In this role, the successful candidate will utilize a wide range of experimental techniques to support our efforts to develop these antibody-based therapies. The position requires strong foundational knowledge of protein chemistry, the ability to work on multiple projects simultaneously, and the enthusiasm to tackle new experimental techniques. | 3/13/2022 |
| 7325 | Orca Bio Sacramento, CA Manufacturing Research Associate BS or MS in Biology or related Exp: 1-2 years |
The Manufacturing Research Associate is responsible for process optimization and cGMP manufacturing activities in the production of cellular therapies in support of clinical studies. Responsibilites Include: Faithfully execute scientific protocols; Develop cell therapy for blood diseases; Optimize cell assays; Use cell separation technologies; Maintain mammalian cell cultures; etc. Perform flow cytometry and analyze dataThe Manufacturing Research Associate is responsible for process optimization and cGMP manufacturing activities in the production of cellular therapies in support of clinical studies. Responsibilites Include: Faithfully execute scientific protocols; Develop cell therapy for blood diseases; Optimize cell assays; Use cell separation technologies; Maintain mammalian cell cultures; etc. Perform flow cytometry and analyze data | 3/13/2022 |
| 7326 | ORIC South San Francisco, CA (Sr.) Research Associate, Biochemistry and Cellular Physiology BS or MS in Biology, Cell Biology, Microbiology, or related Exp: 0+ years |
They will lead research programs and support drug discovery with the goal of identifying targets and developing therapeutics to overcome drug resistance in cancer. This is an ideal position for a researcher eager to participate in drug discovery efforts from target discovery to lead candidate selection with unlimited opportunity for growth in Oncology Research. The successful candidate will participate in the development and implementation of biochemical as well as cellular assays in support of cancer drug discovery and become a key member of highly collaborative cross-functional project teams. | 3/13/2022 |
| 7327 | Pacific Biolabs Hercules, CA Microbiology Lab Technician BS in Microbiology, Biology, or related Exp: 0 years |
The Laboratory Technician will report to Microbiology Management and will contribute to general laboratory testing, sample management, and laboratory maintenance. Primary responsibilities include but, are not limited to the following: Laboratory housekeeping tasks, collecting and processing laboratory test samples, perform equipment preventive maintenance, perform cleanroom preparation and maintenance, media preparation, environmental monitoring, maintenance of departmental logbooks and testing guidelines in accordance with SOPs and cGMP regulations. | 3/13/2022 |
| 7328 | Pacific Biolabs Hercules, CA In Vivo Research Associate BS in Biological Sciences or related Exp: 0-2 years |
The In Vivo Research Associate is a laboratory level job focusing on the development, optimization, and execution of a variety of in vivo (i.e., laboratory animal) and in vitro (i.e., cell-based and noncell-based) test methods. Successful candidates will be familiar with laboratory procedures including the use of analytical balances, calculating and preparing dilutions, pipetting, measuring pH, documenting study activities, and analyzing/interpreting data. The position requires rotating weekend and holiday hours. | 3/13/2022 |
| 7329 | Paraza Pharma Laval, QC Associate Scientist, Chemical Sciences MS in Organic, Medicinal, or Bioorganic Chemistry Exp: 0+ years |
The key responsibilities include: Synthesis of target molecules as part of a medicinal chemistry team; Troubleshoot and optimize reaction sequences; Participation in medicinal chemistry team meetings; Presentation of results to chemistry and project teams | 3/13/2022 |
| 7330 | PCI Pharma Rockford, IL Operations Process Engineer BS in engineering or related Exp: 1-5 years |
This position will work to continuously improve processes and systems that ultimately lead to improved profitability to the company. Using all available Engineering, Lean and Six Sigma tools, this position will work independently and cross functionally to drive out waste and reduce process variability | 3/14/2022 |
| 7331 | PCI Pharma Rockford, IL Microbiologist I BS in engineering, microbiology, biology, or related Exp: 1-5 years |
The primary function of this role is to collect and process environmental samples from across all Rockford facilities using aseptic technique. In addition, this role is responsible for daily monitoring of the Laboratory temperature recorder charts for various equipment in the Laboratory. This role may participate in training of other analysis in techniques for which competency has been demonstrated. | 3/14/2022 |
| 7332 | Pfizer Andover, MA Production Engineer I BS in engineering or related Exp: 0-2 years |
Working with Pfizer’s dynamic engineering team, you will play a critical role in providing engineering and technical support related to the operation, maintenance, installation, startup/commissioning, testing, and qualification of process and automated equipment and systems within a biopharmaceutical manufacturing facility. This may include production equipment such as bioreactors, fermentors, ultrafiltration skids, Clean – In – Place (CIP) skids, and other support equipment. | 3/14/2022 |
| 7333 | Pfizer Andover, MA Process Scientist/Engineer I BS in engineering or science Exp: 0+ years |
Responsibilities: Contribute to completion of project milestones and organize own work to meet project task deadlines; Use operational and technical expertise to assist in troubleshooting activities, technology transfer and start-up activities; Monitor the technical documentation for the production and processes approval; Ensure all production equipment and systems are in compliance with {Current} Good Manufacturing Practices; Manage execution of relevant process activities by following established Standard Operating Procedures | 3/14/2022 |
| 7334 | Pfizer Pearl River, NY Associate Scientist, Cell Culture BS in science Exp: 1+ years |
Responsibilities include: Order laboratory supplies such as plasticware consumables and reagents as needed for daily laboratory operation; Contribute and review documentation associated with protocols and SOPs, including data archiving, data review; Present experimental results at group meetings and project meetings; Write monthly progress report if applicable; Performs job responsibilities in compliance with cGXP regulations; Satisfactorily completes all training in conformance with departmental requirements. | 3/14/2022 |
| 7335 | Pfizer Groton, CT Associate Scientist, Medicinal Chemistry BS in Chemistry Exp: 0+ years |
As an Associate Scientist in Medicinal Chemistry at Pfizer you will play a vital role as a key contributor of a large, multi-disciplinary matrix team from project inception through to delivery of clinical drug candidates. You will provide key contributions to the implementation of medicinal chemistry strategies through development and execution of innovative chemistry and help to revolutionize our approach to the discovery and development of small molecule and synthetically-derived drugs. | 3/14/2022 |
| 7336 | Pfizer Pearl River, NY Associate Scientist, Biofunctional Assays BS in science Exp: 1+ years |
You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support the technology transfer and integration of new laboratory immunoassays into the cGLP space, support assay validation projects and monitor immunoassay lifecycle. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. | 3/14/2022 |
| 7337 | Pfizer Pearl River, NY Associate Scientist, HCID, Vaccines BS in biology, microbiology, immunology, or related Exp: 0-2 years |
You will have the important role to generate high-quality data in a regulated Good Clinical Laboratory Practices (GCLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. The incumbent is responsible for supporting immunoassays in BSL2 and BSL3 conditions. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. | 3/14/2022 |
| 7338 | Pfizer Kalamazoo, MI Process Engineer MS in science or engineering Exp: 1+ years |
Provides technical expertise and operational support for B41 Injectables operation, with focus upon the filling operations. Partners with shop floor colleagues and supervision to ensure smooth and efficient production of a diverse mix of human and animal health injectable products. Assists in equipment troubleshooting activities as needed. | 3/14/2022 |
| 7339 | Phase Genomics Seattle, WA Software Engineer BS or BA in computer science or bioinformatics Exp: 1-4 years |
Phase Genomics is seeking smart, talented, motivated web engineers to design and build the infrastructure and user interfaces that host our revolutionary genomic analysis tools. Our engineers work across a wide range of technologies, from the front end to the back end, designing everything from database-driven web applications to web-based user collaboration tools to massively parallel data analysis systems. | 3/14/2022 |
| 7340 | Complete Genomics San Jose, CA Field Service Engineer BS in engineering or science Exp: 0+ years |
The Field Services Engineer provides onsite and remote service and support to customers. She/He provides feedback and service knowledge to other departments to drive improvements and share information on Instrumentations. The Field Services Engineer performs Service activities at clinical and scientific research sites according to approved written instructions, and documents the activities performed. | 3/14/2022 |
| 7341 | Complete Genomics San Jose, CA Research Associate, Spatial Genomics BS or MS in Molecular and Cellular Biology, Chemistry, Biochemistry, Materials Science or related Exp: 1+ years |
This position is for a self-motivated and detail-oriented Research Associate with hands-on wet-lab experience to support our Spatial Genomics service. The candidate should be able to execute experiments independently, communicate with team players effectively, and interpret and document results in a timely fashion. | 3/14/2022 |
| 7342 | Starr Surgical Monrovia, CA Quality Engineer I MS in engineering or science Exp: 1 year |
Support site production, operations, and quality and R&D teams by addressing emergent issues that might arise due to the operation processes. Serve as the quality representative during any product or process investigation. Lead investigations including root cause analysis and health risk assessment of the identified product or process nonconformities. | 3/14/2022 |
| 7343 | Vesigen Therapeutics Cambridge, MA Research Associate I-II, Tissue Culture Master’s degree in biology or related discipline Exp: 1-3 years |
Vesigen is seeking a creative and highly motivated Research Associate to join our team and help advance the development of the company’s exciting ARMMs technology. The candidate will be an integral member of the R&D team, with opportunities to learn and contribute and develop numerous preclinical programs across several therapeutic areas. | 3/15/2022 |
| 7344 | Vor Biopharma Cambridge, MA Associate Scientist, Analytical Development (Potency Assays BS or MS in a scientific field Exp: 0-3 years |
Vor Biopharma is seeking an Associate Scientist of Analytical Development to assist with developing potency assays for our HSPC and CAR-T gene therapy products. The ideal candidate must have a strong background and hands-on experience with primary cell or tissue culture, ideally with prior exposure to cell biology techniques and protocols. The successful candidate will also be responsible for excellent sterile technique, attention to detail, careful note-keeping habits, and supporting and facilitating method transfer and validation. | 3/15/2022 |
| 7345 | Voyager Therapeutics Lexington, MA Associate Scientist/Senior Associate Scientist, Cell Culture Development Bachelor’s or Master’s degree in chemical engineering, biology, biochemistry, chemistry, biotechnology, and related fields Exp: 0-5 years |
The Technical Operations team is actively researching technologies to improve AAV production and is seeking a highly motivated scientist or engineer to join the Upstream Process Development Group as an Associate Scientist/Senior Associate Scientist. The qualified candidate will have a background and expertise in the manufacturing of biologics. Primary responsibilities include carrying out upstream process development activities for the manufacture of pre-clinical and cGMP grade rAAV vectors. The position includes both bench work and helping mentor less experienced colleagues. The ability to independently design experiments, analyze data and report results concisely as well as taking the initiative to drive Voyager’s projects and manufacturing process are important in this position. | 3/15/2022 |
| 7346 | Voyager Therapeutics Cambridge, MA Research Associate/Senior Research Associate Bachelor's degree Exp: 1-3 years’ |
We are seeking a highly motivated biologist to contribute to our research team at our facility in Cambridge, Massachusetts. This is an ideal position for an individual with experience in in vitro molecular biology assays, who has a can-do attitude and strong work ethic, and thrives in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment. The individual will work in the laboratory and be responsible for experimental execution for research studies supporting cutting edge therapeutic programs and platform discovery research in neurodegenerative disease areas. We are looking for a candidate with hands-on experience with molecular cloning, molecular biology, mammalian cell culture and downstream analysis (e.g. RT-qPCR, western blot). | 3/15/2022 |
| 7347 | Voyager Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Histotechnologist Bachelor’s or Master's degree in Life Sciences or related field Exp: 1-5 years |
Voyager Therapeutics seeks an entry level and highly motivated biologist to contribute to its research team at its facility in Cambridge, Massachusetts. This is a hands-on position for a person committed to helping the group conduct innovative drug discovery research while meeting deadlines and company goals. We are seeking a person who is enthusiastic about biomedical research and can work collaboratively with other scientists and team members. This is an ideal position for an individual strong experience in histological techniques such as tissue grossing, processing, embedding, sectioning and special staining of fresh frozen and formalin fixed paraffin embedded rodents and primate tissues. The successful candidate should thrive in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment. This is a 6 month contract position. | 3/15/2022 |
| 7348 | Voyager Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Neuroscience BS or MS in in Molecular/Cellular Biology, Biochemistry, Pharmacology or a similar field Exp: BS: 1-4 years; MS: 0-3 years |
We are seeking an experienced and highly motivated Research Associate or Senior Research Associate to contribute to our Pharmacology team at our facility in Cambridge, Massachusetts. This is an ideal position for an individual with a strong background in molecular and biochemical assays and methods development, who thrives in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. The successful candidate will be lab based and be responsible for the development, implementation, execution, and analysis of ex vivo and in vitro studies to assess expression, distribution, and pharmacodynamic effects in support of multiple therapeutic programs and platform discovery neuroscience research. | 3/15/2022 |
| 7349 | Westat Group Rockville, MD Research Assistant MS Science Exp: 1 year |
Westat has an immediate opening for a research assistant who will work closely with a multidisciplinary research team for longitudinal studies related to health and aging. The successful candidate will learn the operational protocol and proceedures, data collection instruments, training requirements, and survey methodology for the study. The position is based at our office in Rockville, Maryland with a flexible telework arrangementa | 3/17/2022 |
| 7350 | Xencor Monrovia, CA Research Associate 1 - Flow Cytometry Bachelor’s degree in a relevant biomedical field (immunology, biology, microbiology, molecular biology, cell biology, oncology, etc.). An MS degree i Exp: 1 year |
The Flow Cytometry Laboratory at Xencor is looking to fill an entry level position as a Research Associate I. The ideal candidate will be enthusiastic about maintaining instrumentation, helping users of the Flow Laboratory with their flow cytometry, cell sorting, and data analysis needs, and working with mammalian cells. Position requires the ability to work well with others in a user-oriented collaborative environment. | 3/17/2022 |
| 7351 | Xilio Therapeutics Waltham, MA Research Associate, In Vivo Pharmacology B.S. in the field of Biology, or other related fields Exp: 1+ year |
Xilio Therapeutics is seeking a Research Associate to join our In Vivo Pharmacology group. This individual will be responsible for conducting preclinical studies in animal tumor models (efficacy, PK/PD and MOA studies) to characterize immuno-oncology focused protein therapeutics. They will also perform downstream in vitro assays. | 3/17/2022 |
| 7352 | Xilio Therapeutics Waltham, MA (Senior) Research Associate, Immunology BA or MS in biology, biomedical sciences, or a related subject Exp: 0-1+ year |
Xilio is searching for a Research Associate or Senior Research Associate to join the Immunology group and help enable our cutting-edge immuno-oncology pipeline. This opening serves as an excellent opportunity to contribute to novel therapies that have the potential to help cancer patients, while developing technical skills in a trailblazing IO-focused biotech. | 3/17/2022 |
| 7353 | ZeptoMetrix [Antylia] Buffalo, NY Immunoassay, Scientist I Bachelor of Science (BS) degree in biology, microbiology, or other life sciences program Exp: 1 or more years |
Scientist I will learn, understand, and perform the manufacturing and testing of immunoassay products including raw materials, components, and final products. | 3/17/2022 |
| 7354 | ZYMO Research Irvine, CA Bioinformatics Associate MS BS Bio, Bioinformatics, CompSci, Mathematics, Stats, related Exp: 1 to 3 or more years |
Zymo Research is seeking a Bioinformatics Associate to join our Bioinformatics team. The qualified individual will play a key role in building, maintaining, and executing data-analysis pipelines for Next-Generation Sequencing methods to support Zymo Research’s global product strategy. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 3/17/2022 |
| 7355 | ZYMO Research Tustin, CA Process Engineer BS Exp: 1-2 years |
Zymo Research is seeking a highly motivated individual to join our team as a Process Engineer. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! This position is full-time and is based in the Zymo Research and Development Headquarters in Irvine, CA. | 3/17/2022 |
| 7356 | ZYMO Research Irvine, CA Research Associate – Protein Engineering Group An MS degree or a BS Exp: BS: one-year ; MS: 0 year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field, developing recombinant proteins and peptides production methods. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 3/17/2022 |
| 7357 | ZYMO Research Irvine, CA Research Associate An MS degree or a BS Exp: BS: one-year ; MS: 0 year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field, developing recombinant proteins and peptides production methods. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 3/17/2022 |
| 7358 | ZYMO Research Irvine, Research Associate (RNA Seq team) An MS degree or a BS Exp: BS: one-year ; MS: 0 year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field specifically in the cutting-edge technologies of next-generation sequencing (NGS) and nucleic acids handling. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 3/17/2022 |
| 7359 | Accelerate Diagnostics Tucson, AZ Research Associate, Core Lab Bachelor of Science degree in Microbiology, Molecular Biology, or related life sciences. Exp: 1 year |
The Research Associate is responsible for the routine execution of experiments supporting assay development, technical operations, and core lab. This position can be in different teams including assay development, core lab and technical operations depending upon business needs. Shift: PM (2:00pm - 11:00pm) | 3/17/2022 |
| 7360 | Affinvax Cambridge, MA QC Microbiologist 1 Masters or bachelor’s degree in Microbiology, Biochemistry, or related discipline Exp: 1 to 2 years |
Affinivax is currently seeking a highly motivated QC Microbiologist to use his/her expertise in microbiology-based assays. This position is ideally suited for someone with hands-on experience in microbiology tests, qualification, validation, and environmental monitoring for the clean rooms. | 3/17/2022 |
| 7361 | Genesis Drug Discovery & Development Burr Ridge, IL, Portage, MI, IL Bio-Analytical Scientist Position requires a minimum of a Bachelor’s degree in chemistry, biochemistry, pharmacy or a related discipline, applicable lab bench experience a plu Exp: Entry Level |
Genesis PharmOptima, a member of Genesis Biotechnology Group (GBG), has an immediate opening for a Bioanalytical Scientist. PharmOptima is a Contract Research Organization with proven expertise in ADME/PK, Bioanalysis, and Biochemistry research services to the biotechnology and pharmaceutical industries. The ideal candidate will be able to provide bioanalytical quantitative analysis of test compounds in biological matrices obtained from a variety of studies including preclinical safety evaluations and clinical studies. | 3/18/2022 |
| 7362 | Genesis Drug Discovery & Development Hamilton, NJ Research Associate I Bachelor of Science degree in Life Sciences Exp: 1 to 2 years |
We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 3/18/2022 |
| 7363 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to help confirm contacts in our directory. Mostly just searching on LinkedIN. You should be able to make $20/hr once you figure things out. Must be able to accept payment via PayPal. If interested, send a message through the contact form. Thanks! | 03/14/22 |
| 7364 | PCI Raleigh, NC Pipette Calibration Technician Four-year degree Exp: 0 |
Works with basic laboratory instrumentation, as well as operates computer-based applications utilized in a laboratory environment. Further develops technical skill whenever possible through internal or external training programs; Completes calibrations, qualifications, PMs and changes with GxP documentation in an accurate and timely manner and in accordance with PCI and Client Standard Operating Procedures (SOPs). | 03/17/22 |
| 7365 | PCI Raleigh, NC Calibration Technician I Four-year degree Exp: 0 |
Completes calibrations and qualifications in a safe, timely, and accurate manner, following PCI and client specific policies and proposals; Responsible for proper handling and maintenance of PCI and client equipment, including testing and standards equipment; Identifies project supply and equipment needs and conveys to the appropriate resource to ensure availability; Works to understand client needs and requirements through effective communication and develops client relationships through excellent customer service. Ensures client requests are conveyed to the appropriate PCI management resource and met in accordance with management direction | 03/17/22 |
| 7366 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, Oligonucleotide Chemistry BS/MS degree in Chemistry Exp: 1-5 years |
The Research Associate/Senior Research Associate will be responsible in designing, synthesizing and purifying oligonucleotides for research studies. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 3/7/2022 |
| 7367 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, Oligonucleotide Process Development BS/MS degree in Chemistry Exp: 1-5 years |
The Research Associate/Senior Research Associate will be responsible for developing oligonucleotide purification processes for research and scale-up. We are searching for a driven, enthusiastic, and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 3/7/2022 |
| 7368 | Tessera Therapeutics Somerville, MA Research Associate I/II, Delivery Biology B.A./B.S. in cell biology, molecular biology and/or related fields Exp: 1-2+ years |
The Research Associate I/II will be responsible for tissue culture and in vitro transfections, tissue processing from in vivo mouse studies, and downstream assays to measure effective delivery and efficacy of our Gene Writer™ platforms. This individual will conduct lipid nanoparticle transfections and perform high-content and confocal microscopy analyses and cellular response assays. In addition, the Research Associate I/II is expected to contribute to laboratory upkeep and cultivate a positive and comfortable working environment. We are searching for a driven, curious, enthusiastic, and self-motivated individual. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 3/7/2022 |
| 7369 | Tessera Therapeutics Somerville, MA Research Associate, RNA Analytics - HPLC BS. / M.S. or equivalent in a relevant discipline Exp: 1 - 2 years |
Tessera is seeking a Research Associate (RA) to join the analytical team to characterize synthetic oligonucleotides and mRNA using HPLC. The position will require creativity, resourcefulness, and adaptability. We are searching for experienced, enthusiastic, innovative, and highly motivated individuals who are comfortable working in a fast-paced entrepreneurial environment. | 3/7/2022 |
| 7370 | TriLink Biotechnologies San Diego, CA Manufacturing Associate I Bachelor’s of Science in a scientific field, preferably in Chemistry. Exp: 0 - 2 years |
TriLink BioTechnologies, a Maravai LifeSciences company, is seeking a Maanufacturing Associate I to join our growing team. This role is responsible for producing research and clinical grade components and products by setting-up, cleaning, operating, and maintaining equipment; performing bench chemistry reactions; documenting actions. | 3/8/2022 |
| 7371 | Tris Pharma Monmouth Junction, NJ AR&D Scientist - ALL LEVELS Bachelors degree in Chemistry or related scientific field Exp: 1 year |
AR&D Scientists carry out laboratory work to support AR&D activities and performs special projects as assigned. She/he also carries out laboratory work to support product development and method development. Carries out responsibilities in accordance with the organization’s policies, SOPs, and state, federal and local laws | 3/8/2022 |
| 7372 | TScan Therapeutics Waltham, MA Research Associate/Sr. Research Associate (RA02-5) RA: Bachelor’s degree; SRA: Master’s degree Exp: RA: 0-3+ years; SRA: 0-2+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a highly motivated researcher to join our team as a Research Associate/Sr. Research Associate, supporting our novel target identification and validation workflow in house, with focus on molecular cloning. The ideal candidate should have relevant experience in molecular biology, microbiology, high-throughput cloning, and enjoy fast-paced, collaborative and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 3/9/2022 |
| 7373 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate, Analytical Development (RA06-7) BS/MS Degree emphasis in biology, molecular biology, biochemistry, or related field is preferred. Exp: 0-2+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a Research Associate/Sr. Research Associate in Cellular Analytical Development to join efforts in developing test methods for the company’s novel TCR-engineered T cell therapy products. This newly created role will reside within the Technical Development & Manufacturing department and will report to the Director of Analytical Development. Key activities will include the development and execution of analytical methods to support cellular process development and the tech transfer of in-process, release, and stability-indicating assay methods to QC, amongst others. | 3/9/2022 |
| 7374 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate (RA02-6) Bachelor’s degree or Master’s degree Exp: BS: 0-2+ years; MS: 0-1+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a highly motivated researcher to join our team as Research Associate/Senior Research Associate, supporting our novel target identification and validation workflow in house, with focus on lentivirus packaging. The ideal candidate should have relevant experience in molecular and cell biology, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 3/9/2022 |
| 7375 | Twist Bioscience South San Francisco, CA Research Associate, Antibody Engineering B.S in molecular biology, protein engineering, biological chemistry, or related discipline Exp: 1-year |
We are seeking an outstanding, innovative, and creative Research associate to join our antibody discovery effort. This research associate will play multiple roles within the Biopharma group and will work within a team responsible for antibody discovery utilizing a number of in vitro display technologies, e.g. phage display, ribosome display, and yeast display. | 3/9/2022 |
| 7376 | Twist Bioscience South San Francisco, CA Research Associate, Biopharma Libraries Bachelor's or Master's degree in Molecular Biology, Biochemistry, Chemistry or closely-related field. Exp: 1-3 years |
We are looking for an outstanding Research Associate (RA) to join our Twist Biopharma Libraries team. The Research Associate will support R&D efforts in developing custom DNA-based applications and assays for synthetic biology products. The ideal candidate will be driven and willing to learn new techniques. This position will support projects including high-throughput gene synthesis, high-throughput cloning processes, custom molecular biology, NGS-based QC, etc. The ideal candidate will be eager to learn, be very organized, have excellent molecular biology/biochemistry knowledge and skills, and communicate effectively with peers/management. | 3/9/2022 |
| 7377 | Twist Bioscience South San Francisco, CA Research Associate, Chemistry & Biochemistry M.S. Exp: 1+ year |
Twist Biosciences is looking for a research associate to join our Advanced Development team based in our South San Francisco site. This position will support our Advanced Development R&D team. This may involve running various experiments, the preparation of silicon chips chemical reagents, operating synthesizers and other hardware, supporting protocol development, novel synthetic DNA sample extraction from chips, assay development, post synthesis sample preparation, and data analysis. | 3/9/2022 |
| 7378 | Twist Bioscience South San Francisco, CA Research Associate, NGS Bachelors/ Associates degree in biology, chemistry, biochemistry Exp: 1-3 years |
Twist is seeking a highly motivated individual to help support customers and their Next Generation Sequencing needs. This individual will work closely with R&D and Customer Support teams to help develop custom solutions for various sequencing applications. The candidate will be detail oriented who is compatible with fast paced environments. | 3/9/2022 |
| 7379 | Twist Bioscience South San Francisco, CA Research Associate, NGS Viral Controls B.S. or M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field Exp: 0-2 years |
This position is geared towards working with the DNA and RNA controls product lines. The candidate must be capable of maintaining current products, troubleshooting control fragment assembly issues, and analyzing data related to current and future controls. Up-and-coming scientists that demonstrate self-motivation and enthusiasm for scientific bench work are strongly encouraged. | 3/9/2022 |
| 7380 | Twist Bioscience South San Francisco, CA Research Associate, Process Development B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
We are looking for an outstanding Research Associate to join our Specialty Production Team in South San Francisco. The Research Associate will support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. | 3/9/2022 |
| 7381 | Ultragenyx Pharmaceutical Cambridge, MA Research Associate II, Cell Line Development MS in Biology, Molecular Biology, Biochemistry, Chemical/Biochemical Engineering, or related field Exp: 1-3 years |
Reporting to the head of the Producer Cell Line Team, the Research Associate II will drive CRISPR studies and develop single-cell RNAseq capabilities. Additionally, the Research Associate II will support the molecular and genetic characterization of producer cell lines and further drive HeLa 3.0 platform development. This role typically requires that the majority of the work be conducted on-site and thus will be subject to certain on-site safety protocols during the pandemic. | 3/9/2022 |
| 7382 | Ultragenyx Pharmaceutical Cambridge, MA Research Associate II, Research Analytical Discovery MS in Cell Biology, Molecular Biology, Microbiology, Biochemistry, Virology or related discipline Exp: 0-2 years |
Lead advancement of innovative AAV-based therapeutics; Develop and execute a variety of research methods including molecular, biochemical, biophysical and cell-based assays; Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site and thus will be subject to certain on-site safety protocols during the pandemic; We will assess your level based on your experience before moving forward with full panel interviews. | 3/9/2022 |
| 7383 | United Therapeutics RTP, NC Research Associate I - Lung Function Bachelor’s degree in arts/sciences (BA/BS) in biology, physiology, biomedical engineering, or other related scientific field Exp: 1+ years |
Conduct laboratory studies to aid in the research and development of tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. | 3/9/2022 |
| 7384 | Vero Biotech Atlanta, GA Process Development Engineer – Chemical Master’s degree in Chemical Engineering Exp: · 1+ years’ |
The mission of this position is to extend the capacity of Vero technical operations group to achieve our strategic objectives, including timely product introductions and overall revenue targets. This role will need to effectively work with the VERO N2O4 Operations, Research & Development, Quality, Regulatory, and Supply Chain teams. Key Performance Indicators for this position include attainment of Throughput, Cost of Goods, Product Quality, Inventory targets, and On-time Delivery goals. | 3/9/2022 |
| 7385 | Verve Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Bioanalytical Assays Bachelor’s/ Master’s degree (Biochemistry, Bioengineering, Molecular Biology, Biology, Enzymology, Pharmacology, Chemistry, or related field) Exp: 1-2 years |
Verve is seeking a highly skilled and motivated Research Associate or Senior Research Associate to join our growing bioanalytical team within Preclinical Pharmacology & Toxicology. The primary responsibility of the RA/SRA will be to assist in routine samples analysis and developing new bioanalytical assays (e.g., RT-qPCR assays, ddPCR assays, and other molecular assays) to support the preclinical development of VERVE-101 and VERVE-201 programs. | 3/9/2022 |
| 7386 | ThermoFisher Grand Island, NY Engineer I, Manufacturing Engineer BS in Mechanical, Chemical, or Industrial Engineering Exp: 1+ years |
The Engineer I will apply technical expertise in the support of multiple projects involving the planning, design, reconfiguration, construction and alteration of systems or equipment. Responsibilities: Collaborates with internal and external business partners to develop creative solutions/capabilities related to manufacturing challenges and opportunities; Supports process and equipment enhancements/replacement opportunities through application of advanced engineering principles | 3/5/2022 |
| 7387 | ThermoFisher Frederick, MD Scientist I, Formulations BS in Biology, Chemistry, Biochemistry, or Microbiology Exp: 1+ years |
Responsibilities: Complete production and quality analysis of reagents, components and finished products in accordance with SOPs, work instructions and the Production Schedule to ensure timely availability of cost-effective products of high quality; Effectively communicate and interface with work groups to ensure the completion of daily production; Work in both standard and clean room environments while adhering to room specific PPE requirements; Operate automated and semi-automated equipment | 3/5/2022 |
| 7388 | ThermoFisher Fremont, CA Scientist I, Chemistry BS in science Exp: 0-2 years |
The Formulations Scientist will manufacture products for the Bulk Formulations team and complete associated cGMP documentation. Work with chemicals and biologicals to manufacture calibrators and controls for IVD use. Contribute to the transfer of new products into Manufacturing from R&D. Participates in process improvement projects. | 3/5/2022 |
| 7389 | ThermoFisher West Hills, CA Scientist I, R&D BS in Molecular Biology, Cell Biology, Genetics, Biochemistry, Immunology, or related Exp: 1-2 years |
Responsibilities: Assist with all cell culture aspects using good aseptic techniques - feeding, freezing, thawing and harvesting; Prepare reagents; QC of harvest cells using serological and DNA typing; Cell isolation for EBV transformation; Immunological assays using ELISA and Flow Cytometry techniques | 3/5/2022 |
| 7390 | ThermoFisher Carlsbad, CA Scientist I, Microbiology BS or MS in Life Sciences, or Chemical or Biological Engineering Exp: MS: 0+ years, BS: 1+ years |
This position will work in the cGMP compliant QC Microbiology Laboratory supporting manufacture of biological products. Responsibilities include performing and providing support for functional aspects of the facility such as environmental monitoring (EM), microbiological testing (bioburden, bacterial endotoxin testing, growth promotion, biological indicators, stock cultures), media fills, water testing and validation support. | 3/5/2022 |
| 7391 | ThermoFisher Florence, SC R&D Scientist I BS in Chemistry, Chemical Engineering, or Physics Exp: 0-3 years |
The analytical research & development (AR&D) team has a primary role of developing and validating quality control testing methods for manufacturing support. As part of AR&D’s solid-state lab you will be responsible for method development work related to the physical properties of a drug substance. You will also work closely to support process development and quality control. | 3/5/2022 |
| 7392 | ThermoFisher Carlsbad, CA Scientist I, Cell and Gene Therapy BS in sciences or related Exp: 1-2 years |
The primary focus of the Scientist role will be the design, execution, and analysis of process development experiments to support bioprocessing integration of CAR-T production. The Scientist will work collaboratively within the R&D cell biology team to integrate new technologies, products and protocols for CAR-T production. Additionally, this role may be responsible for the evaluation of new technologies. This is a hands-on position with the candidate expected to spend at least 80% of time at the bench. | 3/5/2022 |
| 7393 | Jordi Labs Mansfield, MA Chemist MS in Chemistry or related Exp: 1 year |
Job duties: 1) Prepare technical reports; 2) Interpret gas chromatograph mass spectrometry (GCMS) and liquid chromatograph mass spectrometry (LCMS) results with a high level of proficiency; 3) Interpret chromatographic data including high performance liquid chromatography (HPLC), gas chromatography (GC), and gel permeation chromatography (GPC) results; 4) Combine results from multiple techniques to identify unknown chemical compounds; etc. | 3/5/2022 |
| 7394 | Jubilant Pharma Spokane, WA Associate, QA Compliance BS in Biology, Chemistry, or related Exp: 0+ years |
The QA Compliance Associate provides support to the company Incident (Deviation), Corrective and Preventive Action (CAPA) program through a complete assessment of Root Cause Analysis (RCA) of incidents/deviations and vendor complaints/issues. Assure product compliance and product safety. Ensure accurate and timely data entry and oversight of the company Quality Systems related to Incident, CAPA and vendor complaint activities. | 3/5/2022 |
| 7395 | Jubilant Pharma Spokane, WA Scientist I BS in science Exp: 0 years |
The QC Scientist I/II/III performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw material/product disposition. Essential responsibilities include: Analyze raw materials, in-process product, or finished product according to established procedures and as directed by the Supervisor; Record results and other salient data in the prescribed manner to meet regulatory requirements; etc. | 3/5/2022 |
| 7396 | Karuna Therapeutics Boston, MA Research Associate, Discovery Informatics BS in Biology, Chemistry, Computer Science Exp: 1+ years |
This critical position will be responsible for managing discovery data in partnership with our discovery team and potential external academic and industry collaborators with the goal of supporting new and existing Discovery staged portfolio programs for advancement towards clinical ready candidates. In addition, the candidate will have excellent communication skills needed to work collaboratively with colleagues across disciplines to help ensure timely execution of studies, collect, and manage resulting data output, and help communicate final data to fellow Discovery scientists and more broadly to internal and external audiences. | 3/8/2022 |
| 7397 | KCAS Shawnee, KS Analyst II - BioProcess LCMS BS or BA in Chemistry, Biochemistry, or related Exp: 1+ years |
The Analyst II is responsible for preparation of reagents and solutions as well as sample processing under required regulatory documentation. Analyzes data, interprets results, operate using LC-MS/MS techniques and contributes to troubleshooting activities. May provide basic training for other laboratory personnel. | 3/8/2022 |
| 7398 | KCAS Shawnee, KS Analyst I - Pharma Discovery BS in Chemistry, Biochemistry, Biology, or related Exp: 0+ years |
As an Analyst I, Pharma Discovery in our GLP bioanalytical laboratory at KCAS, you will leverage your knowledge in scientific principles to be responsible for preparation of reagents and solutions as well as sample processing under required regulatory documentation. You will analyze data, interpret results, and contribute to troubleshooting activities, such as inventory of chemicals, washing glassware, waste disposal and/or general cleanup. You may also provide basic training for other laboratory personnel. | 3/8/2022 |
| 7399 | KCAS Shawnee, KS Analyst I - BioPharma Regulatory LBA BS in Chemistry, Biochemistry, Biology, or related Exp: 0+ years |
The Analyst I is responsible for preparation of reagents and solutions, as well as sample processing under required regulatory documentation. May also analyze data, interpret results or contribute to troubleshooting activities. Conducts sample inventory and carries out lab support duties as assigned, such as inventory of chemicals, washing glassware, waste disposal and/or general cleanup. | 3/8/2022 |
| 7400 | KCAS Shawnee, KS Analyst I - Biomarker Services BS in Chemistry, Biochemistry, Biology, or related Exp: 0+ years |
Responsibilities include: Process and/or analyze samples using ELISA and enzyme activity assays; Prepare and label laboratory solutions; Perform and/or verify calculations related to reagent preparation and/or sample analysis; Conduct sample inventory and verify sample identities; Review information and documentation for accuracy | 3/8/2022 |
| 7401 | KCAS Doylestown, PA Laboratory Technician BS in Biology, Immunology, or Related Exp: 0+ years |
As a Laboratory Technician you will be responsible for the preparation of media, buffers, and reagents within a GLP laboratory environment. You are also responsible for order receipt and reagent/supply restocking of the laboratories, as well as sample receipt under GLP guidelines. | 3/8/2022 |
| 7402 | KemPharm Coralville, IA Laboratory Assistant BS in life sciences Exp: 0 years |
The Laboratory Assistant requires a recent graduate, or student currently pursuing a biotech-related degree, to perform the following responsibilities: Follows standard operating procedures (SOP) for maintaining laboratory equipment and facilities; Assists in the preparation and/or prepares solutions, reagents, starting materials; Performs routine laboratory tests, chemical reactions, and isolation/purification procedures; Coordinates and/or conducts laboratory equipment maintenance and calibration; etc. | 3/8/2022 |
| 7403 | Kodiak Palo Alto, CA Research Associate BS in Cell Biology, Molecular Biology, or related Exp: 1+ years |
The successful candidate will contribute to the development, validation and sample analysis of regulated assays using a range of platforms and analytes. The bioanalytical scientist may also function as the principal investigator of projects and participate in cross-functional team discussions at various stages of research and development, as well as contribution to regulatory submissions. | 3/8/2022 |
| 7404 | Kodiak Palo Alto, CA Research Associate, Protein Production BS or MS in Cell Biology, Biochemistry, Molecular Biology, or related Exp: 1+ years |
The candidate will join the Protein Engineering team responsible for engineering & characterizing antibodies and novel protein formats for the treatment of retinal diseases. The candidate will help drive our research through protein expression and purification. | 3/8/2022 |
| 7405 | Krystal Biotech Pittsburgh, PA Upstream Process Development Research Associate BS in biology or related Exp: 0+ years |
The candidate will support our process development group in the execution of experiments related to the characterization and optimization of viral vector production. The candidate will also support the tech transfer of fully characterized processes to our Manufacturing team. To be successful, the candidate should demonstrate basic knowledge in fundamental mammalian cell culture techniques, show curiosity, initiative, and the ability to work well in a timeline-driven environment. | 3/8/2022 |
| 7406 | Krystal Biotech Pittsburgh, PA Quality Assurance Associate BS in biology or related Exp: 1+ years |
Krystal Biotech is seeking a highly motivated individual to author high-quality documentation to support the implementation of our quality system, GMP manufacturing area, and quality control laboratory. Responsibilities include: Work with internal teams to obtain an understanding of the product and the documentation requirements; Produce high-quality documentation that meets applicable standards and is appropriate for its intended use | 3/8/2022 |
| 7407 | KSQ Cambridge, MA Associate/Sr. Associate Scientist, Exploratory Immunobiology BS or MS in biology, immunology, or related Exp: 0-3+ years |
The candidate will work in a multidisciplinary team to discover and optimize novel immunotherapeutic molecules for the treatment of cancer. Our ideal candidate thrives in a collaborative research environment that demands scientific rigor and technical excellence. The candidate will perform experimental activities and analysis, with mentor supervision and feedback. Applicants with a strong interest in immuno-oncology, T cell immunology are strongly encouraged to apply. | 3/8/2022 |
| 7408 | KSQ Cambridge, MA Sr. Associate Scientist, In Vivo Pharmacology MS in life sciences or related Exp: 0 years |
We seek a motivated and team-oriented individual who will be a key contributor to the KSQ’s IO pipeline, which includes multiple programs involving our eTIL platform, NK cells and autoimmunity. The successful candidate will contribute hands-on technical expertise for all aspects of in vivo pharmacology including model development, efficacy studies and mechanism of action studies to help evaluate IO pipeline candidates and better understand their biology. This candidate will be a key contributor to several stages of drug development, including, target validation, exploratory biology efforts and IND enabling studies. | 3/8/2022 |
| 7409 | KSQ Cambridge, MA Associate Scientist, Target Discovery BS in life sciences or related Exp: 1-3 years |
This skilled scientist will help develop novel gene-editing strategies to enhance our eTIL programs. Experience with modern techniques including CRISPR for genetic engineering and assaying gene function a must (NGS, ddPCR, qPCR, molecular cloning, tissue culture, flow cytometry). Experience in gene editing in cell therapies a big plus. | 3/8/2022 |
| 7410 | KVK Tech Newtown, PA Lab Technician BS in chemistry or related Exp: 0 years |
Primary responsibility is to complete documentation and analytical testing of raw materials, in process materials, stability samples, finished products and product development in a timely manner, while maintaining compliance with cGMP requirements, FDA, OSHA, EPA, and DEA. | 3/8/2022 |
| 7411 | Kyverna Emeryville, CA Research Associate/Sr. Research Associate, Immunology MS in immunology, cell biology, or related Exp: 0 years |
Responsibilities include: Reporting to the Staff Scientist, Immunology, the candidate will Conduct laboratory research to develop candidate CAR-synReg T cell therapeutics, optimize synReg T cell immunoregulatory functions, and target engineered T cells to diseased tissues; Isolate and grow primary human T cells, transduce cells with viral vectors, analyze cell phenotypes by flow cytometry, probe immunomodulatory functions using in vitro and in vivo assays, and track T cell homing in vivo. | 3/8/2022 |
| 7412 | Kyverna Emeryville, CA Research Associate MS in biology or related Exp: 1+ years |
Responsibilities: Reporting to the Process Scientist, T Cell Engineering, the successful candidate will help design and execute unit operations in the production of engineered T cell therapy candidates. The role will involve implementing existing methods for the generation of engineered T Cells, as well as testing novel approaches that can improve the manufacturability and quality of engineered cell products. The candidate will help identify important process parameters that impact the yield and quality of candidate, therapeutic T Cell products and will drive our understanding of how these factors affect critical quality attributes. | 3/8/2022 |
| 7413 | LifeMine Gloucester, MA Research Associate, Microbiology BS in biology, microbiology, mycology, or related Exp: 1+ years |
We are seeking a Research Associate for our Gloucester, MA site with experience handling and cultivating filamentous fungi for preparation of DNA, maintenance of our strain collection, and production of secondary metabolites to support the core research behind LifeMine’s genomically-enabled drug discovery platform. | 3/8/2022 |
| 7414 | Ligand San Diego, CA Associate Scientist I/II, Purification Development MS in Biology, Microbiology, Biochemistry, Biochemical Engineering, or related Exp: 1 year |
The position covers clarification techniques for microbial hosts, such as continuous centrifugation, depth/membrane filtration, followed by purification using chromatography. Position scope extends to bench and pilot scale process development activities, DOE execution, data generation/collation, as well as support for technology transfer to CMO facilities. Individual technical issue management and effective communication are key position attributes. | 3/8/2022 |
| 7415 | Liquidia Morrisville, NC Associate Engineer BS in Engineering or related Exp: 0-2 years |
We are seeking an Associate Engineer to work within cross-functional teams to develop processes for the manufacturing of novel particles for engineered drug delivery. In this role you will be responsible for conducting process development activities geared toward the optimization and continuous improvement of production processes to support R&D, clinical and commercial manufacturing. | 3/8/2022 |
| 7416 | Masy BioServices Hatfield, PA Validation Specialist BS or BA in science or engineering Exp: 0+ years |
Responsibilities for this position involve validation equipment preparation, protocol execution and final report generation. This position will support a wide range of validation activities focused on environmental chambers, including: cryo-freezers, cold rooms, refrigerators, incubators, sterilizers, depyrogenation ovens, stability chambers and warehouses. | 3/10/2022 |
| 7417 | MDxHealth Irvine, CA Product Development Associate MS in science or engineering Exp: 0-3 years |
The Product Development Associate is involved in assisting with the planning, conducting and analyzing experiments leading to validation of diagnostic tests in the field of oncology. The PD Associate works in a team and needs to communicate relevant information to professional colleagues and to participate constructively in discussions that will impact the performances of the final product. | 3/10/2022 |
| 7418 | MDxHealth Irvine, CA Clinical Laboratory Scientist I/II BS in science or related Exp: 1+ years |
The Clinical Laboratory Scientist I or II (CLS I or II) performs a variety of both routine and complex clinical laboratory tests in accordance with established processes and procedures. These require professional level of knowledge to properly execute and analyze results, especially where results are abnormal or atypical. | 3/10/2022 |
| 7419 | Medicomp Melbourne, FL Creative and Collaborative Software Engineer BS in Computer Science or Electrical Engineering, or related Exp: 0+ years |
The Software Engineer will work with the data science team developing software that coordinates data flow through various Machine Learning models. This is an entry level position. The candidate will have the opportunity to work with a great team to learn and grow. Essential Functions: Designing and implementing robust applications, Conduct activities in accordance with the FDA Design Controls | 3/10/2022 |
| 7420 | Cook Medical Bloomington, IN Research and Development Engineering Design Specialist BS in engineering or science Exp: 0+ years |
The Engineering Design Specialist at Cook Incorporated supports the research and development of novel medical devices and works within an interdisciplinary team of engineers, specialists, and technicians to advance the strategic goals of the company. | 3/10/2022 |
| 7421 | Cook Medical Spencer, IN Production Engineer BS in Mechanical or Electrical Engineering, or related Exp: 0+ years |
The Production Engineer plans, directs, and coordinates manufacturing processes for medical device products, and supports Operations in a way to assure a quality product is produced in a timely manner. The Production Engineer works with Operations, Quality Assurance and Regulatory Affairs to improve existing product designs and processes to increase throughput, decrease operational costs, or improve quality. | 3/10/2022 |
| 7422 | Cook Medical Winston-Salem, NC CAPA Engineer BS in Engineering or Science Exp: 0+ years |
The primary purpose of this position is to organize and coordinate the root cause analysis investigations and implementation of Corrective and Preventive Actions for active CAPA projects. Responsibilities include: Lead CAPA Investigations; Determine implementation dates and provide documentation to support effectiveness of proposed corrective and preventive actions; Document CAPA using CAPA software program(s); Interface with cross-functional teams and drive efficient and accurate CAPA completion, etc. | 3/10/2022 |
| 7423 | Morphic Therapeutics Waltham, MA Research Associate (I/II/Sr.), I/O BS or MS in science or engineering Exp: 1+ years |
Morphic Therapeutic is seeking a Research Associate with in vitro and in vivo skills for pre-clinical research in I/O space. The candidate will join a dynamic, multi-disciplinary team of scientists, playing a key role to evaluate new immunotherapeutic strategies and drug candidates. The candidate is expected to be multi-tasking and able to execute experiments with strong attention to detail. | 3/10/2022 |
| 7424 | MPE Sturtevant, WI Manufacturing Engineer BS in Mechanical or Industrial Engineering, or related Exp: 1+ years |
Under the direction of the Director of Operations at Racine Metal Fab (RMF), the Manufacturing Engineer (ME) is responsible for acting as an engineering consultant with Customers, Sales, Supply Chain, Quality, and Operations. This position is accountable for the management of all New Product Implementations (NPI) and Engineering Changes (ECN), and provides assistance with Prototypes. | 3/10/2022 |
| 7425 | Myriad Genetics Salt Lake City, UT Laboratory Technician (Swing Shift) BS in chemical, physical, biological, or medicinal sciences Exp: 0+ years |
Responsibilities: Complying with the laboratory’s technical, administrative and safety policies and procedures; Participating in the laboratory’s quality assurance plan, adhering to quality control and preventive maintenance policies and appropriately documenting these activities; Working as part of a team to produce repeatable quality results; Maintaining a clean and organized laboratory space; Following Standard Operating Procedures (SOPs); Operating high performance liquid handling robots | 3/10/2022 |
| 7426 | Beckman Coulter Life Sciences San Jose, CA R&D Systems Engineer II MS in mechanical, chemical, or biomedical engineering, or physics Exp: 1 year |
We are seeking a highly motivated R&D Systems Engineer to join our dynamic team developing the next generation of acoustic liquid handling instrumentation. Development responsibilities may include data collection and analysis, design verification testing, acoustic drop transfer optimization, process optimization, system specification and design, signal processing, algorithm development, and technology transfer to manufacturing. | 3/1/2022 |
| 7427 | Beckman Coulter Life Sciences Fort Collins , CO Mechanical Engineer - STEM IDEAS Program (May 2022 Graduates) BS or MS in mechanical, biomedical, or computer engineering, or data science, or related Exp: 0-1 years |
iDEAS (Innovation Defines Engineers and Scientists) is a highly competitive, inter-site science and engineering program to jump start your career. Over the span of 18 months, you will have the opportunity to work on 3 different, 6 month long projects in both technical and non-technical functions (Commercial, Marketing and IT). We are looking for Engineers and Scientists that have an interest in R&D or Quality and Regulatory fields. | 3/1/2022 |
| 7428 | Beckman Coulter Life Sciences Indianapolis, IN STEM iDEAS - Rotational Leadership Development Program (R&D Engineer) BS or MS in mechanical engineering, computer science, biology, or related Exp: 0-1 years |
In our STEM iDEAS Rotational Leadership Development Program, you’ll jump into two year-long projects followed by a 6-month project that’s either international or outside your functional/technical area. This particular STEM iDEAS position begins with a project in the Genomics & Automation R&D group in Indianapolis. You will work closely with other engineers and scientists in the Genomics and Automation groups to develop cutting edge new products for our customers. | 3/1/2022 |
| 7429 | Cepheid Lodi, CA Quality/Compliance Specialist I MS science or engineering Exp: 0-2 years |
Responsibilities include: Review records and documents, for completeness and compliance with QSR and ISO requirements; Review batch record to support release of raw materials, work in progress and final products. This includes reagents, components and instrumentation-related products; Generate standard operating procedures to define and improve quality system functions | 3/1/2022 |
| 7430 | Cepheid Newark, CA Process Engineer - Consumables Automation MS in engineering or related Exp: 0-2 years |
The Process Engineer will use their industry experience to design and develop and monitor assembly processes for medical device manufacturing. They will evaluate current capabilities, available technology in the industry, and product requirements to develop new and improve current assembly methods and processes. Use statistical analysis to monitor assembly processes and drive continuous improvement in collaboration with a diverse and highly talented engineering team | 3/1/2022 |
| 7431 | Cytiva Marlborough, MA Project Engineer, Investigations BS in biological, mechanical, chemical, or plastics engineering Exp: 1+ years |
The primary focus of this position is to lead sustaining engineering activities for single-use fluid pathway assemblies used in Upstream processing of biologics based on direct customer input. This position requires the application of design, root cause analysis investigation, product testing, data analysis and report writing to resolve and improve product design, process and quality issues all while working in a cross-functional team environment. | 3/1/2022 |
| 7432 | Cytiva West Jordan, UT Quality Assurance Specialist BS in science Exp: 0+ years |
Responsibilities Include: Assist in the maintenance of company's quality program documentation to ensure conformity to internal and external quality standards (ISO, GMP); Initiates and maintains vendor and customer qualifications; Releases raw materials and finished goods; Meets with vendors, customers, quality representatives, and company personnel to discuss and resolve quality problems as required | 3/1/2022 |
| 7433 | Cytiva Logan, UT Cell Culture Research Associate BS in life sciences, biomedical engineering, or related Exp: 1+ years |
The Cell Culture Research Associate is responsible to carry out laboratory work to support Cytiva Cell Culture Service media and process development projects under supervision. The candidate is required to be proficient in aseptic techniques and have solid hands-on experience with mammalian cell culture. Will be permanently relocated to Cytiva site in Marlborough, MA during 2022. | 3/1/2022 |
| 7434 | Pall 7 possible locations, R&D Leadership Program Associate (Sept. 2022) MS in chemical, mechanical, petroleum, or biomedical engineering Exp: 0 years |
During the two-year program, you will work alongside some of the brightest people in the industry and will be given four, six-month assignments engaging your technical and leadership skills. In these assignments you will experience at first hand many facets of R&D – project management and project team direction; process application studies, product design using tools like CAD or our proprietary in house filter design modules; prototype manufacture and testing; and product transfer to manufacturing. | 3/1/2022 |
| 7435 | Integra Plainsboro, NJ Microbiologist I BS in microbiology or biology Exp: 0-3 years |
Responsibilities Include: Perform and document in-house microbiological testing on all in-process and finished products to comply with acceptance requirements; Perform LAL, water analysis, growth promotion, gram staining, identification of microorganisms and other microbiological testing; Perform and document environmental monitoring in compliance with Standard Operating Procedures | 3/2/2022 |
| 7436 | Integra Boston, MA QC Analyst I BS in biology or chemistry or related Exp: 1-3 years |
Responsibilities Include: Perform chemical assay of solutions as well as general laboratory maintenance; Microbiological testing; Inspection and testing of raw materials, intermediates and final product; Environmental monitoring of clean rooms and water system; Develops and revises SOPs and trains appropriate employees | 3/2/2022 |
| 7437 | Integra Boston, MA Quality Engineer I BS in engineering, math, or science, or related Exp: 1-3 years |
Responsibilities Include: Assist with key Quality Engineering areas of responsibility; Identification and implementation of CAPA; Control of Nonconforming Product process activities (e.g., MRB review/approval); Execution of Risk Management activities | 3/2/2022 |
| 7438 | Integra Plainsboro, NJ Chemist I BS in chemistry or biology Exp: 0-3 years |
Responsibilities Include: Ensure compliance with all company policies and procedures and appropriate regulations, Perform and document instrumental (e.g., UV-VIS, HPLC) and wet chemistry techniques/analyses; Perform laboratory testing, as well as general laboratory maintenance, including in-process and final product release testing and stability testing | 3/2/2022 |
| 7439 | IQVIA Indianapolis, IN Associate Scientist - Large Molecules BS or MS in chemistry, biology, or biochemistry Exp: BS: 1+ years, MS: 0+ years |
Responsibilities Include: Under supervision, plan and prepare certain predefined assays and/or analyses and carry out study conduct; Assist with compilation of results. Assist with protocol and/or report writing; Assist in basic equipment maintenance and operational verification of laboratory equipment; Assist in archiving of data and results | 3/2/2022 |
| 7440 | IQVIA Durham, NC Immunoassay Scientist BS in chemistry or related Exp: 1+ years |
Responsibilities Include: Execution of ELISAs, RIAs, cell-based assays and other immunoassay techniques as required in a BSL2 lab under direction of project leader; Learn and perform required laboratory techniques using novel and established protocols and Standard Operation Procedures under the direction of project leader; Perform assays under direction of the project leader; May act as project leader depending on experience/training level | 3/2/2022 |
| 7441 | IQVIA Austin, TX Assay Development Associate Scientist BS in science Exp: 1+ years |
The Associate Scientist for Assay Development is responsible for assisting with experimental execution in support of assay/method development programs. | 3/2/2022 |
| 7442 | IQVIA Durham, NC Immunology Scientist/Senior Scientist BS in chemistry or related Exp: 1+ years |
Responsibilities Include: Execution of ELISAs, cell-based assays and other immunoassay techniques as required in a BSL2 lab under direction of project leader; Learn and perform required laboratory techniques using novel and established protocols and Standard Operation Procedures under the direction of project leader; Perform assays under direction of the project leader. (2 positions available) | 3/2/2022 |
| 7443 | IQVIA Wayne, PA Data Operations Associate BS in science, data science, or related Exp: 0+ years |
This position assists in managing EDC implementation for contracts with CRO’s, clinical sites, clients and investigators. This position receives incoming enrollment data, conducts data review, and completes necessary edits, management of the visit payment process for all assigned clinical trials and ensuring site satisfaction. | 3/2/2022 |
| 7444 | IQVIA Austin, TX Laboratory Data Analyst BS in science or data science Exp: 0+ years |
Supports data centric requests generated both internal to the company and from customers. The Lab Data Analyst reports to a Supervisor or Manager. The incumbent initiates, and develops processes expected to result in partial or complete project fulfillment related to products or needed information. This is a remote, home based position requiring 2-4 days a month be spent in the Austin office. | 3/2/2022 |
| 7445 | IQVIA Ithaca, NY Associate Scientist - Sample Prep BS in Life Sciences Exp: 0+ years |
Performs a wide variety of increasingly complex technical laboratory experiments and procedures related to sample preparation. This can include method development/optimization and troubleshooting experiments, validation, and study sample preparation in addition to the preparation of solutions and reagents. Assists in maintaining lab equipment, supports lab safety, and complies with IQVIA procedures and Good Laboratory Practice (GLP) requirements, as applicable. | 3/2/2022 |
| 7446 | Sirnaomics Gaithersburg, MD Research Assistant Scientist - Formulation BS or MS in Pharmaceutics, Chemistry, Chemical engineering, Biomedical engineering, or related Exp: 1+ years |
The well-qualified candidate will assist in running formulation experiments using Sirnaomics siRNAs and nanoparticles. Responsibilities: Perform nanoparticle formulation preparation and analytical experiments to characterize the peptide, siRNA and nanoparticles; Assist in the development of new delivery platforms, validation and testing for siRNA delivery; Assist in peptide and/or oligonucleotide conjugation, nanoparticle bioconjugation for targeted delivery | 3/2/2022 |
| 7447 | Merck West Point, PA Associate Engineering Scientist BS in biology, chemistry, biochemistry, or related Exp: 1 year |
We are seeking a highly motivated colleague to join our team as a scientist for separations-based assays in sponsorship of our large molecule programs. This position will work in a GXP environment under the direction of a laboratory guide and will be expected to execute large molecule methods (e.g. UV/Vis, light scattering, and other bio-physical methods). The candidate will work with team colleagues to deliver high quality results supporting assay development, validation/ transfer, and regulatory submissions. | 3/3/2022 |
| 7448 | Merck Elkton, VA Associate Specialist Engineering Upstream Process Development BS in biochemical engineering or related life science or engineering field Exp: 0+ years |
The Process Development Associate Specialist will be responsible for assisting in driving the development, optimization and characterization of current and future fermentation and cell culture processes at the laboratory scale. | 3/3/2022 |
| 7449 | Merck West Point, PA 3rd Shift Associate Specialist - Maintenance & Utilities BS in engineering or science Exp: 1+ years |
Is responsible to provide day-to-day equipment and facility engineering support for assigned area including vaccine bulk manufacturing, and/or associated facility/utilities mechanical support. Assigned tasks include support and monitoring of equipment performance and maintenance, propose & develop equipment and facility improvements and troubleshoot process equipment to ensure reliable, compliant and efficient operations. Actively ensures compliance to current Good Manufacturing Practices, Safety, and Environmental regulations while achieving operating cost goals. | 3/3/2022 |
| 7450 | Merck Elkton, VA Associate Specialist, Engineering (multiple openings) BS or MS in biology, chemistry, computer science, or chemical, biomedical, or mechanical engineering, or related Exp: 0 years |
Responsibilities Include: Providing technical support for vaccine, biologic, and sterile manufacturing processes in the form of data analysis, troubleshooting, problem-solving, report writing; Supporting change control implementation; Learning new processes and procedures; Performing shift work as needed; Conducting technical investigations and analyses | 3/3/2022 |
| 7451 | Merck West Point, PA Engineering Scientist MS in biology, chemistry, biochemistry, or related Exp: 1 year |
This position will work in a GXP environment under the direction of a laboratory guide and will be expected to execute large molecule methods (e.g. UV/Vis, plate-based spectrophotometric and/or fluorescent, light scattering, and other bio-physical methods). The candidate will work with team colleagues to deliver high quality results supporting assay development, validation/ transfer, and regulatory submissions. | 3/3/2022 |
| 7452 | Merck Rahway, NJ Scientist MS in chemistry, pharmaceutical science, life science, or related Exp: 0 years |
Responsibilities Include: Support execution of scientific studies to support development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes using both traditional and advanced analytical tools; Troubleshoot challenges associated with the drug development through active collaboration with cross-functional project teams; Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner. The ideal applicant would have experience with HPLC, dissolution characterization, mass spectrometry, and basic statistical analysis. | 3/3/2022 |
| 7453 | Merck Boston, MA Scientist, Oncology Discovery MS in biological sciences or immunology Exp: 0+ years |
We are seeking a highly qualified and motivated scientist with a strong background in oncology research to join our Oncology Discovery team in Boston. Primary responsibilities will include designing and carrying out experiments in the laboratory to build and support projects in the early discovery pipeline. An ability to communicate clearly and collaborate effectively with colleagues in the discovery group as well as scientists from different disciplines will be essential. | 3/3/2022 |
| 7454 | NeoGenomics Multiple, Clinical Laboratory Technologist I BS in cytogenetics, or other science Exp: 1+ years |
In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. Available in Houston, TX and other locations | 3/3/2022 |
| 7455 | NeoGenomics Ft. Myers, FL Clinical Laboratory Technologist Trainee BS in life sciences or physical sciences Exp: 1-3 years |
A Cytogenetic Technologist Trainee in the Cytogenetics department will enter the CA certified Cytogenetic Training Program. At the successful completion of the training program and passing the ASCP exam, trainees are promoted to the position of Clinical Laboratory Technologist. During the year, trainees work on a lab rotation learning each aspect of the lab - slide-making, harvesting, culture set-up, reagent preparation, equipment maintenance and karyotyping procedures. Trainees also develop their microscopic analytical skills through multiple phases of microscope training. | 3/3/2022 |
| 7456 | NeoGenomics Multiple, Clinical Laboratory Technologist - Flow Cytometry BS in chemical, physical, or biological science Exp: 1+ years |
NeoGenomics is looking for a Technologist for the Flow Cytometry department, no prior Flow experience needed for this position that will work a Tues-Sat, 12p – 830p shift. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 3/3/2022 |
| 7457 | NeoGenomics Aliso Viejo, CA Laboratory Technician I BS or BA in life science or physical science Exp: 0-1 years |
As a Laboratory Technician you will work under the direct supervision of licensed personnel, or within a training environment. You will assist with responsibilities associated with processing specimens for clinical testing and will provide general support for the laboratory following established policies and procedures. | 3/3/2022 |
| 7458 | NeoGenomics Aliso Viejo, CA Molecular & Research Development Technologist BS with strong background in chemistry, biology, and physics Exp: 1+ years |
You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. At least one year of laboratory experience/training/training course is required. | 3/3/2022 |
| 7459 | NeoGenomics Houston, TX Quality Assurance Specialist I BS in sciences Exp: 1+ years |
The Quality Assurance Specialist is directly responsible for overseeing materials accepting activities and study verification activities as part of the Quality Assurance Unit for Pharma Services. This position collaborates with the Quality Team to maintain a constant state of regulatory compliance and ensuring customer satisfaction by providing outstanding quality services. | 3/3/2022 |
| 7460 | Perrigo Bronx, NY Production Engineer BS in engineering Exp: 1+ years |
As a Production Engineer at Perrigo, you will provide production engineering support for day-to-day operations of a lean six sigma pharmaceutical manufacturing facility. Initiate and drive continuous improvement efforts in assigned process area. Works on plant floor with the Specialists, Plant Manager, Supervisors, Engineering and other staff to troubleshoot technical problems with manufacturing or packaging equipment or process problems in production areas. | 3/4/2022 |
| 7461 | Perrigo Allegan, MI Continuous Improvement Engineer BS in engineering, pharmaceutical science, chemistry, or related Exp: 0+ years |
The Continuous Improvement Engineer provides technical support as it relates to incident/deviation investigations for all commercialized products at Perrigo facilities within Michigan. | 3/4/2022 |
| 7462 | Perrigo Allegan, MI Associate Scientist - Analytical R&D MS in chemistry or pharmaceutical science Exp: 1-2 years |
The Professional in this role will be responsible for development of assay, impurities, dissolution, and physical characterization methods for oral and nasal drug products. There is an expectation of both direct hands-on laboratory work as well as mentoring/training of colleagues. Our focus is on the development of analytical methods for small molecules in support of research and characterization of new and reformulated drug products. Chief techniques include HPLC/UPLC-UV stability-indicating methods with various separation chemistries. | 3/4/2022 |
| 7463 | Perrigo Multiple, Associate Scientist - Biopharmaceutics and Scientific Substantiation MS in pharmaceutical science Exp: 0-3 years |
We are seeking a highly motivated, qualified, research-oriented professional that will bring in expertise, resourcefulness, and creative approaches to support and further a diligent scientific substantiation program. The job requires designing and/or executing studies to establish bioequivalence, product functional claims, clinical data analysis, scientific literature review and technical writing. | 3/4/2022 |
| 7464 | Perkin Elmer Hopkinton, MA Associate Manufacturing Electrical Engineer BS in Electrical, Mechanical, Chemical, or Bio Engineering, or Mechatronics, or Manufacturing Exp: 0-1 years |
Responsibilities Include: Develop, implement, sustain operating procedures for assembly, test and safe handling of Medical Devices; Leverage Lean principles to assist in the design and execution of new and existing manufacturing processes, methodologies and equipment layouts to improve overall equipment effectiveness; Establish and maintain data collection and performance measurements to track performance in key areas; Ensure that the product manufacturing processes are in compliance with regulatory requirements and the site’s quality management system. | 3/4/2022 |
| 7465 | Perkin Elmer San Diego, CA Research Associate I, Diagnostics BS in life sciences Exp: 1+ years |
This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report. | 3/4/2022 |
| 7466 | Sestina Bio Pleasanton, CA RA II/III/SR Bioengineering BS/BA/MS Degree Exp: 1+ year |
Sestina Bio is looking for a flexible and talented research associate to join our Biological Engineering group to build world class cellular factories using cutting edge genetic engineering, analytics, and data science technologies. This researcher will work collaboratively with other Bioengineering team members across functions and will be primarily responsible for designing and creating DNA parts, executing strain engineering and selection strategies, preparing samples for analytical evaluation, and helping to develop novel laboratory tools and methodologies. The ideal candidate has experience in yeast strain engineering, general knowledge of cellular metabolism, and some experience working with high throughput sample preparation. | 3/2/2022 |
| 7467 | SMITHERS Gaithersburg, MD Associate Research Scientist MS Exp: 1 year |
Smithers Pharmaceutical Development Services is building a state-of-the-art translational science facility in Gaitherburg, MD and is actively seeking an Associate Research Scientist to join our team. The candidate should bring a keen curiosity and desire to take a key role in development, validation, and documentation of novel nucleic acid analysis methods under guidance of a Research Scientist. Experience in tissue culture, RNA and DNA sample preparation, amplification, and characterization is highly desired. This role will also ensure that basic lab management functions such as equipment maintenance and an adequate supply of materials and reagents is maintained. Relocation expenses will not be provided. | 3/2/2022 |
| 7468 | SMITHERS West Trenton, NJ Associate Research Scientist MS in biology, life sciences, or chemistry field Exp: 1 year |
Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance. PDS works with customers to develop new methods, validate existing methods, and perform the assays necessary to analyze samples from patients on more than 100 clinical trials. PDS is seeking an Associate Research Scientist to join our team. The Associate Research Scientist performs data analysis and various assays according to SOP with reliability while applying and meeting GLP, GCP, and/or CLIA requirements. This position assists with training and technical guidance to more junior scientist and ensures that the lab, materials, and equipment are maintained. | 3/2/2022 |
| 7469 | Smith and Nephew Mansfield, MA Quality Engineer 1 BS in Engineering Exp: 0 - 2 years |
The Quality Engineer I is responsible for supporting the Smith & Nephew Quality Management Systems at the Mansfield manufacturing site. The Quality Engineer I will ensure that the Regulations, Standards and Guidelines are complied with ensuring that finished devices will be safe and effective and otherwise in compliance with the Federal Food, Drug, and Cosmetic Act (the act). | 3/2/2022 |
| 7470 | Sofregen Medical Framingham, MA Quality Engineer Bachelor’s degree in scientific discipline Exp: 0-2 years |
Sofregen Medical is seeking a Quality Engineer to join our Manufacturing team and support the production of Sofregen’s commercial silk-based medical device platform. The Quality Engineer plays a vital role in the maintenance of the Quality Management System as well as the daily operation of the laboratory. Duties will include maintaining a system to track equipment calibration & maintenance, environmental monitoring, inventory management, receiving and incoming inspection, and authoring routine Quality Control documentation (e.g. deviations, standard operating procedures (SOPs), batch records, etc.). The Quality Engineer will further collaborate with Manufacturing members to provide general support to critical processes. | 3/2/2022 |
| 7471 | Spherotech Lake Forest, IL Quality Control Associate Bachelor's degree in Chemistry or related field Exp: 1 year |
Duties include final product inspection, documentation, Quality Control testing etc. | 3/2/2022 |
| 7472 | Spotlight Therapeutics Heyward, CA Research Associate (RA/SRA) - Protein Engineering BS/MS in molecular biology, biochemistry, or microbiology, or a related discipline Exp: 1 year |
We are seeking a biochemist/molecular biologist to join our Platform Technology group. Our group is building a new class of biologics from a toolbox of CRISPR/Cas systems, affinity domains, and cytosolic delivery technologies. This position is an outstanding opportunity to contribute directly to our core protein engineering and production capabilities, as well as work directly with our cell biologists, immunologists, and gene editing experts. | 3/3/2022 |
| 7473 | Spotlight Therapeutics Heyward, CA Research Associate (RA/SRA) - Cell Biology BS/MS in molecular biology, cellular biology, or related field Exp: 1-2 years |
We are looking for an enthusiastic research associate to join our Biology team in the monogenic diseases group. This candidate will help develop cell models, be responsible for testing engineered RNPs, and evaluate downstream editing. The candidate may also help in identifying disease targets and will screen guides for different disease indications. This individual will also work across different teams to advance numerous projects. The candidate will have opportunities for professional growth and development in a fast-growing biotechnology start-up. | 3/3/2022 |
| 7474 | Spotlight Therapeutics Heyward, CA Research Associate (RA/SRA) - IO Cell Biology BS/MS in molecular biology, cellular biology, or related field Exp: 1-2 years |
This position will focus on cell biology and preclinical development in cancer immunotherapy and other disease areas, utilizing Spotlight’s proprietary delivery platform to modify disease relevant genes in vivo using CRISPR. Primary responsibilities will include design and execution of a wide-range of cell-based assays to support pre-clinical data packages to enable progression of development candidates, as well as supporting discovery programs. A main focus will include support of programs utilizing primary cell culture, flow cytometry based readouts and mechanistic assays. This position will also include assistance with downstream evaluation of in vivo experiments. This position requires a minimum of 1-2 years of laboratory experience, with demonstrated expertise in cell biology. This position requires the ability to lift 25 lbs and may involve travel to a nearby off-site vivarium. Prior experience with immuno-oncology, gene editing, molecular biology, and/or biologics is a plus. | 3/3/2022 |
| 7475 | Strand Therapeutics Cambridge, MA Associate Scientist, LNP Formulations Development B.S./M.S. in Pharmaceutical Sciences, Chemistry, Chemical Engineering or other relevant scientific discipline. Exp: 1-3 years |
We are looking for a highly motivated and innovative candidate for the role of Associate Scientist, LNP Formulation Development. The expectation is that the candidate will have experience in formulation and characterization of LNPs (Lipid Nanoparticles). The candidate will be expected to work in an innovative, fast-paced, cross-collaborative biotech environment and contribute in multi-disciplinary team activities to advance our platform. | 3/3/2022 |
| 7476 | Strand Therapeutics Cambridge, MA Associate Scientist, mRNA Process Development BS Degree with emphasis in Biochemistry, Chemical Engineering, Molecular Biology, Bioengineering, Molecular Medicine, Genetics or related field prefer Exp: 1-2+ years |
We are looking for a highly motivated and innovative candidate for the role of Associate Scientist, mRNA Process Development. The expectation is that the Associate Scientist will have experience independently executing mRNA process development experiments and production efforts. Reporting to Scientist, Process Development, the right candidate will be a strategic thinker that brings a leadership presence and enthusiasm for Strand along with a desire to conquer new challenges. | 3/3/2022 |
| 7477 | Sutro Biopharma South San Francisco, CA Research Associate, Process Development Downstream (South San Francisco, CA) BS/MS in scientific discipline Exp: 1- 5 years |
The candidate hired for this position will join a productive and professional downstream process development team. You will be supporting the development of purification processes for scale up and tech transfer to GMP manufacturing. | 3/3/2022 |
| 7478 | Sutro Biopharma South San Francisco, CA Research Associate, Upstream Process Development (South San Francisco, CA) BS/MS in Biochemistry, Bioengineering, Chemical Engineering, or other relevant disciplines Exp: 0-3 years |
Sutro Biopharma, Inc. is looking for a talented Research Associate to join our Upstream Process Development team. You will be working to develop and scale up pharmaceutical protein production processes to internal and external manufacturing sites. | 3/3/2022 |
| 7479 | Sword Diagnostics Chicago, IL Research Associate I BS or BA in biology, biochemistry or related field Exp: 1 -3 years |
Plan experiments with guidance from supervisor • Perform complex and critical laboratory experiments (primarily ELISA) with accuracy and precision • Analyze experiment results and recommend potential follow-on experiments • Follow all established company processes and procedures • Prepare buffers and other chemical solutions as needed • Other duties and responsibilities as assigned | 3/3/2022 |
| 7480 | T2 Biosystems Lexington, MA Senior Research Associate - Microbiology M.S. in microbiology or molecular biology. Exp: 1-2 years |
This position is to fill a need within our Microbiology group working in our Lexington, MA location. The individual filling this role will be responsible for providing general expertise in the areas of microbiology and bacterial physiology. The Senior Research Associate will provide a lead technical role in the development of laboratory protocols for the cultivation of pathogenic organisms and preparation of contrived patient samples for the development of diagnostic assays. | 3/3/2022 |
| 7481 | Taconic Biosciences Rensselaer, NY Senior Laboratory Specialist Molecular Analysis - 1st Shift Bachelor’s Degree from a four-year college or university Exp: 1-3 years’ |
The Senior Laboratory Specialist performs a variety of molecular assays on animal samples and must be able to generate high-quality results in a timely manner. This individual should be comfortable working in a high-throughput environment and be able to use proper judgement to make technical decisions on assay performance issues. | 3/3/2022 |
| 7482 | Taconic Biosciences Rensselaer, NY Senior Laboratory Specialist Molecular Analysis - 2nd Shift Bachelor’s Degree from a four-year college or university Exp: 1-3 years’ |
The Senior Laboratory Specialist performs a variety of molecular assays on animal samples and must be able to generate high-quality results in a timely manner. This individual should be comfortable working in a high-throughput environment and be able to use proper judgement to make technical decisions on assay performance issues. | 3/3/2022 |
| 7483 | TCR2 Therapeutics Cambridge, MA Research Associate, T-Cell Process Development B.S./M.S. degree in immunology, cell biology or similar discipline Exp: 0-2 years |
We are looking for a Research Associate to join the T Cell Process Development team to work on cutting edge TRuC T cell manufacturing process, and to support regulatory filings. You will report to our Scientist, T Cell Process Development and work closely with the Analytical Development group and other teams as needed. This is an excellent opportunity for career development, working closely with experienced scientists in a fast-paced and highly collaborative environment to support the production and in vitro characterizations of novel autologous and allogeneic TRuC-T cells programs. | 3/3/2022 |
| 7484 | Tenaya Therapeutics South San Francisco, CA Research Associate II, PD M.S. in a biological science or chemical engineering Exp: 1-2 years |
We are seeking a motivated Research Associate for our Technical Operations, Process Development Group. In this role, you will perform key production and characterization activities to support Upstream Process Development; routine productions; troubleshoot and optimize production unit operation and assays as needed; assist in the development of new characterization methods to determine precursor and in-process material purity and identity; perform housekeeping tasks such as lab equipment maintenance and supply ordering. | 3/3/2022 |
| 7485 | Tenaya Therapeutics South San Francisco, CA Research Associate/Senior Research Associate, Gene Therapy A Bachelor’s or Master’s degree in Molecular Biology, Cell Biology, Biochemistry, or related discipline. (Research Associate) Exp: 1 year |
Tenaya has an immediate need for a Research Associate or Senior Research Associate to support the Gene Therapy team. Tenaya is seeking a creative, self-motivated individual with a passion for experimental science and teamwork. The ideal candidate is a self-starter and problem-solver who will work closely with the team to drive the company’s future success. | 3/3/2022 |
| 7486 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to help confirm mailing addresses and phone numbers for the companies we list. Can be a bit boring, but you should be able to make $20/hr once you figure things out. Must be able to accept payment via PayPal. If interested, send a message through the contact form. Thanks! | 2/24/2022 |
| 7487 | Interius BioTherapeutics Philadelphia, PA Research Associate, Analytical Development BS in science Exp: 1+ years |
As an early career Scientist, you will bring your scientific skills to our team that is responsible for developing methods to support our internal lentiviral vector programs. Working closely with others, you will take what you know and apply it each day in the lab. As the successful candidate, you will embrace the “roll-up your sleeves” biotech start-up culture where you are not only an amazing scientist, but also an essential collaborator and team player. | 2/19/2022 |
| 7488 | Interius BioTherapeutics Philadelphia, PA Research Associate, Discovery MS in biological sciences or engineering Exp: 0-2 years |
As a highly motivated and creative Scientist, you will bring your scientific curiosity and hands-on laboratory skills to support our internal lentiviral vector programs. Working alongside other Scientists, you will play a critical role in supporting discovery activities. Bringing solid skills in molecular biology and mammalian tissue culture, you enjoy working on several projects at a time and are comfortable with interactions across different roles and levels in the organization. | 2/19/2022 |
| 7489 | Pace Analytical Maplewood, MN Lab Analyst, Microbiology BS in biological sciences or related Exp: 1-3 years |
This position will actively support food safety and quality assurance through the use, and validation of, pathogen detection products. The analyst will prepare and evaluate samples using aseptic technique to ensure products meet specifications. The products being monitored are crucial to maintaining consumer safe food supply chains. | 2/19/2022 |
| 7490 | Pace Analytical Eagan, MN Lab Technician BS in chemistry, chemical engineering, or science Exp: 0-2 years |
The main function of a laboratory technician is to conduct chemical and physical laboratory tests to assist scientists and engineers in making qualitative and quantitative analyses of solid and liquid materials used in the institutional cleaning chemical market. The laboratory technician will be supporting multiple projects and project teams with a focus on machine warewashing chemicals, equipment, and ware performance testing. | 2/19/2022 |
| 7491 | Pace Analytical Maplewood, MN Product Development Technician (Lab Technician) BS in biology, physics, or related Exp: 0-2 years |
Responsibilities include: Planning and undertaking controlled experiments; Sample preparation, Data analysis, and interpretation of results; Operating and maintaining a variety of lab instruments; Documenting results following cGMP requirements; Oral and Written presentation of data and results Performing peer review of data | 2/19/2022 |
| 7492 | Pace Analytical Eagan, MN Chemist - Stability/Formulation BS in chemistry or biochemistry Exp: 0-2 years |
Gain experience in an R&D team that works on procurement driven projects to deliver cost savings, supply security, and growth in a fast-paced team environment. The main function of this individual is to prepare stability samples and conduct product stability using qualitative and quantitative procedures in the laboratory. Responsibilities include performing routine and repetitive quality control analysis and observations along with testing product performance. | 2/19/2022 |
| 7493 | Invenra Madison, WI Research Associate, Antibody Discovery BS or MS in biology, biochemistry, or related Exp: 1+ years |
The successful candidate will use their knowledge of molecular biology, biochemistry, or microbiology to work within the Discovery group, which operates cross-functionally to discover antibodies, optimize and characterize lead drug molecules, and implement new practices to improve Invenra’s antibody discovery platform. | 2/19/2022 |
| 7494 | Invenra Madison, WI Research Associate, Innovation BS in chemistry, biochemistry, or related Exp: 1+ years |
This individual will report to Senior Scientist, Innovation, and will work across teams to advance understanding of a rapidly growing library of antibody – antigen binding interactions using SPR and BLI. The individual in this role will use biophysical, biochemical, and statistical principles to implement and optimize the role of high-throughput approaches into multiple steps in the drug development pipeline at Invenra. | 2/19/2022 |
| 7495 | Invenra Madison, WI Research Associate, Translational Bioprocess BS in biochemistry or related Exp: 1+ years |
Invenra is seeking a highly motivated Research Associate to join our Translational BioProcess team to support the company’s protein purification pipeline. The successful candidate will use their knowledge of protein biochemistry to work with the group to produce highly purified protein needed for in vitro and in vivo efficacy and preclinical studies. | 2/19/2022 |
| 7496 | Invicro Needham, MA Laboratory Assistant, Advanced Pathology Services BS in biological science Exp: 1-2 years |
Work as part of Lab Services team to provide support for all routine Histology and IHC work pertaining to delivery of CAP/CLIA and GLP-like oriented lab services offered to external partners, including BioPharma, Academia, and Oncology Research Centers | 2/19/2022 |
| 7497 | Isoplexis Branford, CT Research Associate BS or MS in biochemistry, cell biology, or related Exp: 1-3 years |
Responsibilities include: Research and execute experiments to drive innovations in the IsoPlexis assay and microfluidic device; Perform screening assays to characterize new antibody pairs for new immunoassays; Developing and troubleshooting new immunoassays for commercialization | 2/19/2022 |
| 7498 | Charles River Rockville, MD Research Associate I, Virus Production BS in biology, cell biology, molecular biology, or related Exp: 0+ years |
As a part of Virus Production, the Research Associate I is responsible for performing cell culturing, transfections, cell harvesting and purification with AAV and production procedures | 2/19/2022 |
| 7499 | Charles River Memphis, TN Biologics Manufacturing Associate I BS in science or engineering Exp: 0-1 years |
The Manufacturing Associate 1 is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays, as necessary. Must be able to work in a clean room environment that potentially in equipment (including blood, tissues, and needles). | 2/19/2022 |
| 7500 | Charles River Rockville, MD Research Associate II, Upstream Process Development MS in Chemical or Biomolecular Engineering, cell biology, biochemistry, biotechnology, or related Exp: 0-2 years |
The Research Associate II, with minimal supervision, will be responsible for execution of experiments to optimize conditions in upstream process to develop robust, scalable, and reproducible processes for cell seed train expansion and viral vector production. He/she will also work on sourcing reagents, equipment, and materials for specific projects, performing in-process assay. | 2/19/2022 |
| 7501 | Charles River Rockville, MD Research Associate I Downstream - Plasmid Production BS in biology, cell biology, molecular biology, or related Exp: 0-2 years |
The Research Associate I Downstream is responsible for working with the Downstream Scientist on all aspects of downstream DNA plasmid preparation development, including organized record keeping and material stock management. | 2/19/2022 |
| 7502 | Charles River Northridge, CA Research Associate I BS in biological sciences Exp: 1 year |
This position is responsible for the evaluation of human blood products for manual or automated cell isolations, product manufacturer, and cell culture. Perform QC testing and create a certificate of analysis (COA) for products manufactured. Record isolation details on a processing worksheet using good documentation practices. Operate flow cytometer and basic lab equipment. | 2/19/2022 |
| 7503 | Charles River Memphis, TN Manufacturing Associate - Cell Therapy BS in science Exp: 0-1 years |
The Manufacturing Associate I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays, as necessary. Must be able to work in a clean room environment that potentially in equipment (including blood, tissues, and needles). Must have ability to perform algebraic math. | 2/19/2022 |
| 7504 | Charles River Rockville, MD Research Associate I Upstream - Plasmid Production BS in biology, cell biology, molecular biology, or related Exp: 0-2 years |
The Research Associate I Upstream is responsible for working with the Upstream Scientist on all aspects of upstream DNA plasmid preparation development, including organized record keeping and material stock management. Responsibilities include: Prepare and conduct E. coli culture experiments including medium preparation, transformation, and small scale and large-scale culture; Monitor and sample fermentation bioreactor by performing optical density and DNA yield measurements. | 2/19/2022 |
| 7505 | Baxter Round Lake, IL Electrical Engineer I BS in electrical engineering or related Exp: 0 years |
You will contribute to the development of creative electrical solutions to challenging problems associated with the design of multi-device systems within the medication delivery portfolio. | 2/22/2022 |
| 7506 | Baxter Mountain Home, AK Process Engineer BS in Engineering Exp: 0 years |
Responsibilities include: Provide engineering support to all assigned processes; Act as technical resource to assist in plant process improvement; Manage/organize other technical resources in the implementation of process improvement projects | 2/22/2022 |
| 7507 | Baxter Allston, ON Chemist I - (Afternoon Shift, Tues-Sat) BS analytical chemistry, biochemistry, or related Exp: 0-1 years |
Perform analytical chemical analysis to ensure products meet required standards using instrumental and wet chemical techniques according to specifications. Compile analysis reports by entering results into the Laboratory Information Management System (LIMS) approving them and forwarding to the Document center. | 2/22/2022 |
| 7508 | Baxter Marion, NC Quality Lab Associate I - Microbiology BS in Microbiology or related Exp: 0-2 years |
Responsibilities include: Perform sampling to support the Environmental Monitoring Program; Use laboratory instrumentation and computer systems to collect and record data; Perform advanced assays requiring precise analytical skills and understanding of microbiological principles | 2/22/2022 |
| 7509 | Baxter Round Lake, IL Quality Associate I - Chemistry Lab BS in chemistry or related Exp: 1+ years |
Responsible for managing documentation within the chemistry lab. A functional understanding of FDA, ISO, and Quality systems is required. | 2/22/2022 |
| 7510 | Baxter Cleveland, MS Facilities Engineer I BS in Mechanical, Chemical, or Electrical Engineering Exp: 1+ years |
The engineer must manage/implement projects related to plant facilities/utilities including but not limited to energy conservation, electricity, HVAC, process compressed air, steam, potable water, chilled water, pest control, and water for injection (WFI). This role also must ensure that these utilities are operating at the most cost-efficient level. | 2/22/2022 |
| 7511 | Baxter Mountain Home, AK Quality Engineer I BS in engineering Exp: 0 years |
Leads or assists in developing and implementing new machines/processes and improvements to existing methods. Support department execution of CAPA investigations with use of DMAIC processes and technical writing skills. | 2/22/2022 |
| 7512 | BD San Diego, CA Quality Engineer I BS in engineering (mechanical or electrical preferred) Exp: 1-2 years |
You will facilitate teams in identifying, documenting, assessing, correcting and preventing quality issues using risk analysis and root cause analysis tools. You will be responsible for quality planning and establishing and maintaining metrics to improve quality system processes and process capability. | 2/23/2022 |
| 7513 | BD San Jose, CA Manufacturing Engineer I BS in engineering (mechanical or electrical preferred) Exp: 0-3 years |
The Manufacturing Engineer (ME) is responsible for generating manufacturing documentation, processing change orders, supporting Instrument Operations Engineering staff. Ensures required documentation for new materials is in place for initial builds and testing using the ECM process. | 2/23/2022 |
| 7514 | BD Covington, GA Quality Engineer I - Post Market Surveillance BS in engineering or science Exp: 1-3 years |
The Quality Engineer, Post-Market Surveillance (PMS) is primarily responsible for executing and coordinating the day-to-day operations of the post-market surveillance program and related processes. Additionally, this position executes various quality engineering tasks in support of Quality Assurance and Design Control. | 2/23/2022 |
| 7515 | BD Lexington, MA Research Associate BS or MS in science Exp: 1+ years |
BD Lexington is currently seeking a Research Associate who will be involved in many aspects of producing and developing biomaterials, including the analysis, production, isolation, purification and testing of biomaterials within well-defined guidelines. The Research Associate will need to use appropriate analytical tools to characterize and qualify the biomaterials, such as gas chromatography (GC), gel permeation chromatography (GPC) and mechanical testing. | 2/23/2022 |
| 7516 | BD San Diego, CA Research Associate II BS in biology or related Exp: 1-3 years |
Performs routine and complex laboratory tasks and procedures relevant to custom products and services in the Custom Technology Team. They will perform a variety of routine experimental protocols and procedures to fulfill custom manufacturing requirements that include, but are not limited to formulations, experimental design, product testing/analysis, and results reporting. | 2/23/2022 |
| 7517 | BD Covington, GA Lab Technician BS in Microbiology or related Exp: 1+ years |
Responsibilities include: Product and component bioburden testing, Environmental monitoring, Product and component sterility testing, Bacterial endotoxin testing, Biological indicator testing, Cytotoxicity testing | 2/23/2022 |
| 7518 | BD Columbus, NE Quality Engineer I BS in engineering Exp: 0-5 years |
Support Quality and Production groups by using process and regulatory knowledge combined with a data driven approach to problem solving. Become a subject matter expert in application of statistical tools, measurement systems analysis, and root cause analysis. Take ownership of projects and drive to completion, whether working independently or in a team. | 2/23/2022 |
| 7519 | Boston Scientific Maple Grove, MN Chemist I BS in chemistry Exp: 0-1 years |
The Chemist I will help with development, validation, and transfer of analytical methods which meet internal and regulatory requirements for medical devices and combination products. They will support the new product development process through method development and testing support. The Chemist I will also be responsible for serving internal BSC analytical lab customers and maintaining lab instruments and test methods. | 2/23/2022 |
| 7520 | Boston Scientific Maple Grove, MN Engineer I, Mfg. Job BS in engineering Exp: 0-2 years |
Provide support to the manufacturing organization by facilitating efficient operations within the production area, to optimize existing processes, and to ensure that production goals are met. Monitors performance of equipment, machines and tools and corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. | 2/25/2022 |
| 7521 | Beckman Coulter Diagnostics Chaska, MN Manufacturing Scientist II MS in science Exp: 0-2 years |
The Manufacturing Scientist II for Beckman Coulter Diagnostics is responsible for leading and implementing projects that will deliver value to the company, facilitate growth and meet cost, quality, and delivery objectives. Responsibilities Include: Lead simple immunoassay process improvement projects that ensure product quality while achieving direct material cost savings; Perform assay testing in laboratory using Access2 and DxI instrumentation. (Hybrid Position) | 2/25/2022 |
| 7522 | Beckman Coulter Diagnostics Miami, FL Development Scientist II MS in Chemistry, Biochemistry, or Molecular Biology Exp: 0-2 years |
Responsibilities Include: Provide technical support and expertise to manufacturing and R&D; Solve issues, handle product non-conformances, rework instructions, redline and collaborate with Quality Assurance and Quality Control to secure the release of Urinalysis reagents; Investigate, conduct experiments, and write technical reports related to chemical reagents | 2/25/2022 |
| 7523 | Beckman Coulter Diagnostics Carlsbad, CA Development Scientist II MS in biology, chemistry, or related Exp: 0-2 years |
The Development Scientist will support the manufacture of clinical chemistry reagents including design changes, failure investigations and Verification/Validation studies. In addition, this role will act as a liaison between Development and current production, facilitating the transfer process and assisting in troubleshooting activities. This individual will also work on future development project initiatives for the department as project priorities and manufacturing support allow. | 2/25/2022 |
| 7524 | Cepheid Lodi, CA Laboratory Compliance Associate MS in science Exp: 0 years |
Responsibilities include: Ensure laboratory environment and practices comply with guidelines set forth by company and regulatory agencies; Establish and implement GMP and GLP practices and procedures; Lead by example and serve as functional expert in the area of laboratory compliance and safety | 2/25/2022 |
| 7525 | Aldevron Madison, WI Associate Scientist II, Analytical Development - Madison, WI BS in biology, molecular biology, chemistry or related Exp: 0-2 years |
The Associate Scientist II, Analytical Development executes and analyzes analytical tests for characterization of proteins. He/she will work closely with team members to understand the test requirements and ensure that results fall within these specifications. Duties may also include assay design and development activities. | 2/25/2022 |
| 7526 | Cepheid Newark, CA Manufacturing Support Engineer MS in engineering or related Exp: 0-2 years |
The associate will lead and coordinate medium to large scale investigations with guidance from senior associates and management. In addition, the associate will develop expertise in risk and impact assessment and provide guidance to development and implementation teams on technical requirements and project direction. | 2/25/2022 |
| 7527 | SAMDI Tech Chicago, IL Research Assistant B.S. in biology, biochemistry, chemistry, or related field Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. | 2/22/2022 |
| 7528 | Sanarus [Hologic] San Diego, CA Research Associate 1 B.A./B.S. Molecular Biology, Chemistry, Biochemistry or related field. Exp: 0 - 2 years |
Hologic is seeking a Research Associate 1 responsible for designing and performing experiments while collaborating and communicating effectively. | 2/22/2022 |
| 7529 | Sanofi Pasteur Swiftwater, PA Research Associate - Vaccine M.Sc. Specialized degree in biological sciences from an accredited University Exp: 1yr |
Experience with the safe use and handling of radioactive materials. Direct responsibility for training and maintaining the radiation safety program with Global Clinical Immunology. Function as an authorized user and assistant site Radiation Safety Officer (RSO). Responsible for performing laboratory testing/support activities associated with a given project or task, including, but not limited to the accurate and timely recording of all data using specified formats, assist with the generation or revision of documentation associated with laboratory activities/processes. they may also be responsible for the review/analysis of data in conjunction with senior personnel, assisting with troubleshooting, investigational studies, and more independently driven studies. | 2/22/2022 |
| 7530 | Sanofi Pasteur Lexington, MA mRNA, Research Associate, Pre-Clinical Plasmid Production M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology) Exp: 1-3 years |
As an experienced molecular biologist, you will be supporting the design, development and implementation of a robust plasmid growth, extraction, and purification process for preclinical supercoiled and linearized plasmid production. | 2/22/2022 |
| 7531 | Sanofi Pasteur Waltham, MA mRNA, Research Associate, HT mRNA Production MS degree required Exp: 0-3 years |
We are seeking a highly motivated and scientifically rigorous candidate who will focus on mRNA synthesis, mRNA characterization, and supporting Sanofi mRNA vaccine programs. This position will give the successful candidate exposure across a broad range of mRNA therapeutic applications and functions within the organization. | 2/22/22 |
| 7532 | Sanofi Pasteur Waltham, MA mRNA, Research Associate II/Senior Research Associate-Plasmid Production M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology) Exp: 1-3 years |
As an experienced molecular biologist, you will be responsible for production a wide range of plasmid constructs with high quality and reproducibility, independently work on plasmid design, construction, purification, characterization. | 2/22/2022 |
| 7533 | Sanofi Pasteur San Diego, CA Principal / Senior Research Associate – Purification, Downstream MS degree Exp: 1 year |
We are seeking a Principal Research Associate / Senior Research Associate to join our Protein Sciences team. This individual has a hands-on role performing downstream process development and scale-up for molecules expressed in our semisynthetic expression platform. This will entail development of primary recovery, refolding, purification, filtration, and formulation operations. The Principal / Senior Research Associate will also author technical documents (reports, tech transfer documents, SOPs), present data to key stakeholders, and participate in troubleshooting. | 2/22/2022 |
| 7534 | Sanofi Pasteur Waltham, MA mRNA, Senior Associate Scientist, Preclinical Immunology Masters degree Exp: 1 year |
As an experienced mRNA vaccine scientist, you will be in charge of Design and execute preclinical research on LNP/mRNA vaccine candidate. | 2/22/2022 |
| 7535 | Sanofi Genzyme Framingham, MA Manufacturing Specialist I Bachelor’s Degree Exp: 1 year |
The Manufacturing Specialist I uses knowledge of compliance and GXP manufacturing processes to be a contributor in the upstream production of clinical drug substance materials in a GMP environment while also participating in activities related to compliance and validation. | 2/22/2022 |
| 7536 | Sanofi Genzyme Orlando, FL Associate Scientist Master’s Degree Exp: 1 year |
Kiadis, a Sanofi Company is seeking a highly motivated individuals with solid training in immunology or related field to join our group located in Orlando, Florida, USA, as an Associate Scientist or Sr Associate Scientist, commensurate with experience. This individual will apply scientific expertise in immunology of primary human cells to support the development of NK cell therapeutics in oncology. | 2/22/2022 |
| 7537 | Sanofi Genzyme Framingham, MA Process Engineer II Master’s degree in engineering or science Exp: 1 year |
The successful candidate will work with a group of scientists and engineers responsible for the support of commercial mammalian cell culture processes to a diverse network of manufacturing facilities at external partners. Key responsibilities may differ among employees with the same job title and may change over time in accordance with business needs. | 2/22/2022 |
| 7538 | Sanofi Genzyme Waltham, MA Senior Associate Scientist - Protein Science Master’s Degree Exp: 1 years |
The Research department at Sanofi – Rare and Neurologic Diseases is seeking a highly motivated scientist to join their protein science group. The position focuses on protein chemistry, including protein production and characterization to support preclinical research programs. The incumbent will be an integral contributor to research project teams and will work within a multi-disciplinary environment. The position is located in Waltham, MA and will relocate to a brand-new research building in Cambridge, MA in Q2 2022. | 2/22/2022 |
| 7539 | Sanofi Genzyme Waltham, MA mRNA, Research Associate, Gene Synthesis M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology) Exp: 1-3 years |
As an experienced Plasmid DNA Research Associate, you will be responsible for supporting the efforts to establish a high throughput gene synthesis workflow initiating with design and ending in analytical methodologies. | 2/23/2022 |
| 7540 | Sarepta Therapeutics Dublin and Columbus, OH Research Associate I/II, Gene Therapy R&D B.S. degree in Biology or related field Exp: 1-3 years |
The Research Associate I (RAI) provides critical laboratory support for all research teams through preclinical animal tissue and sample collection work at the Ohio Genetic Therapies Center of Excellence. The RAI assists in the coordination of effort across teams in order to facilitate efficient and quality sample collection. This role requires laboratory expertise/training in small animal handling and experience in anatomy is preferred. The RAI also assists with downstream sample processing when required. | 2/23/2022 |
| 7541 | Scanogen Baltimore, MD Chemical and Biomolecular Engineer Chemical Engineering degree Exp: 1+ years |
Scanogen is looking for a motivated and skilled engineer to join our R&D team. We are a rapidly-growing start-up company developing a nucleic acid detection platform that will change how diseases are diagnosed. We need highly driven and inventive individuals. | 2/23/2022 |
| 7542 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 2/23/2022 |
| 7543 | Scorpion Therapeutics South San Francisco, CA Research Associate, Biology BS/MS in Biology or a related field. Exp: 1-3 years |
We are seeking a highly motivated research associate to join our dynamic biology drug discovery team in South San Francisco. This candidate will serve a critical role in establishing and running cell-based assays to inform target biology and help drive our small molecule drug discovery programs. This position is ideal for a talented, highly motivated and results driven individual who will thrive in a fast-paced, innovative, start-up environment. | 2/23/2022 |
| 7544 | SDIX Newark, DE Biotechnician I BS/BA degree in biology, chemistry, or related field such as veterinarian studies Exp: 0 to 3 years |
Maintain laboratory in proper working order through organization and procurement of supplies, routine maintenance of laboratory equipment, organization and maintenance of reagents, and general laboratory hygiene. Verify and ensure that proper processes and procedures are followed in accordance with SOPs. Support manufacturing aspects of SDIX’s products by executing protocols, utilizing basic knowledge of biology, chemistry, laboratory equipment and computer software. | 2/24/2022 |
| 7545 | SDIX Windham, ME Biotechnician I BA/BS in biology, chemistry or related field such as veterinary studies Exp: Up to 3 years |
This position supports manufacturing of SDIX’s products by executing protocols using basic knowledge of biology, chemistry, laboratory equipment and computer software. The Biotechnician I is responsible for conducting operations using various laboratory techniques, organizing and procuring supplies, and maintaining a clean and safe work environment. | 2/24/2022 |
| 7546 | Seracare Life Sciences [LGC Clinical Diagnostics] Cumberland, ME Manufacturing Chemist I (36483) Bachelors degree in life science field or other related science or medical curriculum Exp: Entry-Level |
The Manufacturing Chemist I fulfils the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 2/24/2022 |
| 7547 | Glytec Waltham, MA Quality Systems Engineer BS/BA in health information management, quality systems, software, or biomedical engineering Exp: 0 years |
The Quality System Engineer is a critical member of Glytec’s Quality and Regulatory team and works closely with the Director of Quality and Regulatory Compliance to maintain the company’s quality management system (QMS). This includes supporting other departments (Product Management, Software Engineering, Customer Support, etc.) in complying with FDA Title 21 Part 820 & 11 as well as any other applicable regulatory requirements. | 2/12/2022 |
| 7548 | Genapsys Redwood City, CA Laboratory Technician - New Science Grads Welcome BS in biology, molecular biology, chemistry or related Exp: 0-2 years |
The Laboratory Technician plays a pivotal role in the company by generating quality reagents in a consistent and reproducible manner to support the research staff and the commercialization of the product. We are looking to expand the current production capacity and to dramatically increase the level of quality control (stability studies, guardbanding, performing Sequencing QC on our platform, etc.) in the Product Development department. | 2/12/2022 |
| 7549 | Gene Codes Ann Arbor, MI Application Programmer BS in computer science Exp: 0 years |
An energetic developer with strong collaboration and communication skills. Candidates proficient in C++, preferred. Profesional experiance with boost, STL, and Qt, and developing cross-platform applications on Windows and Mac OS X are a plus. A Bachelor's degree in Computer Science or equivalent experience is required. | 2/12/2022 |
| 7550 | Genedit South San Francisco, CA Research Associate/Sr. Research Associate, Chemistry, Platform Program BS or MS in Chemistry, Biochemistry, Chemical Biology, Chemical Engineering, Biomedical Engineering, or Material Science & Engineering Exp: 0-2 years |
GenEdit is seeking a highly self-motivated and goal-oriented Research Associate/SRA with experience in organic synthesis of bio-synthetic polymer and/or complex organic molecule characterization to join our team. This position will also require experience in polymer and/or macromolecule characterization utilizing various separation and detection techniques in support of research, regulatory and business efforts. | 2/12/2022 |
| 7551 | Grail Raleigh-Durham, NC QC Research Associate I/II BS in Science or Engineering Exp: 1+ years |
GRAIL is seeking a Research Associate for the LabOps Manufacturing Sciences and Technology team (MSAT), who will be primarily responsible for materials quality control (QC) and associated tasks. The ideal candidate is a detail-oriented, exceptional team player with hands-on laboratory experience. | 2/12/2022 |
| 7552 | Gritstone Bio Cambridge, MA Senior Research Associate, Discovery MS in science or engineering Exp: 0-2 years |
Gritstone bio is seeking a research associate to help discover novel T cell targets for multiple infectious disease and oncology programs. The primary role of the research associate is to collaborate within and across teams to further develop and optimize a high-throughput epitope discovery platform to drive the therapeutic program and support key company initiatives. | 2/12/2022 |
| 7553 | GRO Biosciences Cambridge, MA Research Associate/Senior Research Associate, Application Sciences BS or MS in biology, microbiology, biotechnology, synthetic biology, systems biology, biological engineering, or related Exp: MS: 0 years, BS: 1+ year |
GRO Biosciences (GRObio) is hiring a Research Associate (RA) / Senior RA to advance the company’s recoded organism technology. Recoded organisms enable efficient production of proteins using an expanded amino acid alphabet. Regular activities will include planning and carrying out experiments throughout our product development pipeline, including cell line development, biomass generation, protein purification, protein characterization, and bioassays. | 2/12/2022 |
| 7554 | Guardant Palo Alto, CA Lab Automation/Process Engineer ll- TissueNext BS or MS in engineering or science Exp: MS: 1+ year, BS: 1-3 years |
You will be developing and implementing high-efficiency workflows using lab automation and advanced liquid handling platforms to process samples in our clinical diagnostics and research laboratory. You will be collaborating with other Process Engineers and Scientists on a Technology Development team to help optimize assay performance and increase the future capabilities of the TissueNext™ product. | 2/12/2022 |
| 7555 | Guardant Redwood City, CA Reagent Manufacturing Associate BS/BA in biomedical science, clinical science, or related Exp: 1+ years |
We’re looking for a Reagent Manufacturing Associate to receive, label, document and prepare reagents for the clinical laboratory. The nature of the work requires excellent attention to detail, effective written and verbal communication skills, the ability to multi-task, be flexible with tasks and schedules and the ability to work independently in a team environment. | 2/12/2022 |
| 7556 | Halozyme San Diego, CA Research Associate 1, Product Development (Contract) BS in science Exp: 0-2 years |
This position supports laboratory activities associated with method development/ troubleshooting/qualification and characterization, covering a wide array of analytical techniques such as chromatography, spectroscopy, activity/potency assays, and wet chemistry. | 2/12/2022 |
| 7557 | Halozyme San Diego, CA Process Development Associate 1 (Contract) BS in science Exp: 0-2 years |
The Process Development Associate -Contract is a member of the Process Development team within the Manufacturing Science and Technology group at Halozyme and supports laboratory activities associated with the development and execution of scalable protein purification processes, including for harvest clarification, column chromatography, tangential flow filtration, and viral clearance steps. | 2/12/2022 |
| 7558 | Integrity Bio (Curia) Camarillo, CA Manufacturing Associate BS in Science or Engineering Exp: 1 year |
Interested in breaking into biotech drug development? Integrity Bio is a great place to take your university lab experience and learn cutting edge industry skills. Integrity Bio, Inc. specializes in biologics formulation development and drug product manufacturing. The Manufacturing Associate will be responsible for the manufacture of pre-clinical/clinical products. (Job ID 2000673) | 2/12/2022 |
| 7559 | Curia Worcester, MA Associate Scientist, Vector Technologies BS in Biochemistry, Biology, or related Exp: 1+ years |
We are searching for a talented individual to join our Vector Technologies Team as an Associate Scientist. The successful candidate will be responsible for executing projects within the laboratory, writing study/research plans, and summarizing data to clients and colleagues via technical reports. | 2/12/2022 |
| 7560 | Curia Hopkinton, MA Associate Scientist, Pharma Assays and Analytics BS or MS in Biochemistry or related Exp: 1-5 years |
We are rapidly growing and seeking a self-motivated individual to join our Pharma Assays and Analytics team as an Associate Scientist/Scientist. Validate and Perform Cell-based and Enzyme-based assays and related procedures using manual and automated liquid handling equipment. (Job ID 2000823) | 2/12/2022 |
| 7561 | Curia Camarillo, CA Quality Assurance Associate BS in Biochemistry, Chemistry, Microbiology, Molecular or Cellular Biology, or Biology Exp: 6 months-1 year |
Under general supervision, the role provides support and compliance oversight to MFG and QCL staff in the execution of their processes, procedures, and use of quality systems. Duties include batch record review, SOP and MP revision approval, and work order approval. (Job ID 2001140) | 2/12/2022 |
| 7562 | Curia Hopkinton, MA Associate Scientist I, PDM MS in Biochemistry, Biophysics, Biology, Chemistry, or Chemical Engineering Exp: 0-1 years |
We are seeking a motivated biochemist with experience in classical and contemporary purification procedures for a variety of biologics. The incumbent will also be working with fellow scientists in developing effective processes for large scale purification of biomolecules. (2000824) | 2/17/2022 |
| 7563 | Curia Albuquerque, NM Process Engineer I BS in Biology, Chemical Engineering, or related Exp: 0-3 years |
The Process Engineer I will be responsible for facilitating the tech transfer of client processes and executing engineering functions including design, scale-up document controls. (2001031) | 2/17/2022 |
| 7564 | Curia Albuquerque, NM Quality Control Microbiologist I BS in science Exp: 1-3 years |
The Quality Control Microbiologist I perform quality activities in support of product production and releases. The QC Microbiologist I performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. (Job ID 2001259) | 2/17/2022 |
| 7565 | Curia Belmont, CA Research Scientist I - Microbiology BS in science Exp: 0 years |
Essential Duties: Perform general laboratory cleaning and organization; Control the inventory of samples and materials; Perform routine equipment maintenance; Construct and clone DNA (e.g. gene synthesis, subcloning, mutagenesis, bacterial cell culture); Perform PCR, screen clones, analyze sequence dataEssential Duties: Perform general laboratory cleaning and organization; Control the inventory of samples and materials; Perform routine equipment maintenance; Construct and clone DNA (e.g. gene synthesis, subcloning, mutagenesis, bacterial cell culture); Perform PCR, screen clones, analyze sequence data | 2/18/2022 |
| 7566 | HemoSonics Durham, NC Associate R&D Engineer BS in Engineering or related Exp: 0+ years |
HemoSonics, LLC is seeking an Associate R&D Engineer who will be responsible for assisting in the design and development of in vitro medical diagnostic devices. | 2/15/2022 |
| 7567 | Herophilus San Francisco, CA Research Associate II BS in biological sciences Exp: 0+ years |
We are seeking a highly motivated Research Associate II to join our Biology team. You’ll work with a team of scientists and engineers and carry out the following responsibilities: Perform molecular biological assays, such as qPCR, Flow Cytometry, Western Blot and/or Immunofluorescence staining and imaging according to Standard Operating Procedures; Perform drug screens using manual and automation equipment; ... | 2/15/2022 |
| 7568 | Hologic Marlborough, MA R&D Engineer BS in Electrical Engineering or other engineering Exp: 0-3 years |
We are looking for a talented Product Engineer that will play a vital role in supporting the continuous improvement of our GYN Surgical Systems portfolio. Typical responsibilities include: requirements analysis, root cause investigations, and support for the integration of electrical, mechanical, and software sub-system components. Performing and supervising testing, data analysis, drawings, documentation and reporting of engineering studies may be assigned. | 2/15/2022 |
| 7569 | Hologic San Diego, CA Quality Engineer 1 BS in Bioengineering/Biomedical Engineering, Molecular Biology, Chemistry, or related Exp: 0-2 years |
Customer Product Support is seeking a Quality Engineer 1 to assist with investigations and help resolve complex customer complaints. Experience working in a GMP environment is a plus. | 2/15/2022 |
| 7570 | Hologic San Diego, CA Research Associate 2 MS in Molecular Biology, Chemistry, Biochemistry or related Exp: MS w/ thesis: 0 years; MS: 1 year; BS: 2+ years |
Hologic is seeking a Research Associate 2 responsible for designing and performing experiments while collaborating and communicating effectively. | 2/15/2022 |
| 7571 | Humacyte Durham, NC Process Development Associate 1 BS in biology, chemistry, or related Exp: 1+ years |
The Process Development Associate 1 will be a hands-on position, performing experimental protocols within the Process Development lab for Humacyte’s regenerative vessels. | 2/15/2022 |
| 7572 | Humacyte Durham, NC Research Associate 1 (New Product Development) BS in biology, biochemistry, chemistry, biomedical or chemical engineering, or related Exp: 0-2 years |
The Research Associate will have numerous roles that primarily include designing and conducting experiments to support product development, performing data analysis and technical writing, assist in the coordination and organization of on-going research programs, and support of laboratory activities through maintenance and ordering of supplies and equipment. | 2/15/2022 |
| 7573 | iFyber Ithaca, NY Laboratory Technician BS in science Exp: 1+ years |
The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements | 2/17/2022 |
| 7574 | IGM Biosciences Mountain View, CA Research Associate I / II / III BS or MS in Cell Biology, Biochemistry, or related Exp: 1-3 years |
We are looking for a Research Associate with a background in Cell Biology or Biochemistry to join our growing and friendly team during this exciting time in our expansion. You will play an integral role in the antibody discovery and validation for the development of novel immuno-oncology therapeutics. In this position, you will perform protein characterizations and cell-based immunoassays, think creatively to solve problems, and work productively as part of a team. | 2/17/2022 |
| 7575 | Immortagen Coralville, IA Bioinformatician MS in computer science, informatics or bioinformatics Exp: 1+ years |
Candidates should have a Master’s degree or higher in computer science, informatics or bioinformatics with at least one year of experience in computational genomics. Prior experience in the analysis of tumor next generation sequencing data is highly desirable. | 2/17/2022 |
| 7576 | Immuneering San Diego, CA Research Associate BS or MS in science Exp: 1-3 years (preferred) |
The ideal candidate is quality and process-oriented, flexible and must enjoy the challenges of working in a fast-paced, start-up biotechnology company with diverse people and drug programs. The Research Associate is responsible for performing research and development experiments for projects and products in collaboration with others. Regularly exercises technical discretion in the design, execution and interpretation of experiments that contribute to project goals. | 2/17/2022 |
| 7577 | ImmuneID Waltham, MA Research Associate/Laboratory Technician - Platform BS in biology, biochemistry, or other life sciences Exp: 0-2 years |
As a member of the Platform team, the Laboratory Technician/Research Associate will support experiments to profile immune disease drivers. They will work closely with Scientists and Research Associates to screen clinical samples using ImmuneID’s proprietary platform. | 2/17/2022 |
| 7578 | ImmuneID Waltham, MA Research Associate/Senior Research Associate BS in biology, biochemistry, or other life sciences Exp: 0-2 years |
As a member of the Immunology team, the Research Associate will provide support in developing and running experiments to understand the biology of autoimmune diseases and therapies. They will work closely with Scientists to address the day-to-day needs of ImmuneID’s laboratory environment in a timely manner, maximizing research productivity and efficiency. | 2/17/2022 |
| 7579 | Imperative Care Campbell, CA Process Development Engineer BS in engineering: mechanical, biomedical, or similar Exp: 0-5 years |
This position will be assigned to assist in the product development process by defining, characterizing, optimizing, and validating stable, robust and capable processes for neuro-interventional medical devices. Responsibilities will include creative problem solving, critical thinking and application of engineering principles, process characterization, design of experiments, analysis of data, equipment documentation and qualification, process documentation and validation. | 2/17/2022 |
| 7580 | InBios Seattle, WA Manufacturing Associate I - ELISA BS in life sciences Exp: 0 years |
Requirements: Good knowledge of general lab procedures and equipment use and care; Familiar with GMP; Able to adhere to SOPs and documented procedures; Experience with Microsoft Office. Position responsibilities include work in a Biosafety Level 2 lab (BSL-2). | 2/17/2022 |
| 7581 | InBios Seattle, WA Manufacturing Engineer I BS in mechanical engineering or electrical engineering Exp: 0 years |
Job duties include: Evaluation of machine logic and controls to troubleshoot equipment and identify process improvement opportunities; Leads teams to identify root cause of manufacturing failures using structured problem solving. Applies root cause fixes to prevent reoccurrence. | 2/17/2022 |
| 7582 | InBios Seattle, WA Quality Assurance Associate I BS or MS in engineering Exp: MS: 0 years; BS: 1+ years |
Job duties include: Under the guidance of senior QA staff, execute FAT/SAT and IQ/OQ/PQ validations for manufacturing equipment; Lead staff trainings to ensure continued adherence to cGMP; Lead review of quality records and set up DMRs and DHRs. | 2/17/2022 |
| 7583 | InBios Seattle, WA Quality Control Assistant - Biotech BS in Chemistry, Biology, Bioengineering, or related Exp: 0-1 years |
Job duties include: Perform fill volume inspections and bacterial contamination testing for assembled liquid goods; Review and approve raw materials specification documents for completeness; Inspect components and kit labeling for clarity and accuracy. | 2/17/2022 |
| 7584 | InBios Seattle, WA Quality Control Associate I BS or MS in Chemistry, Biology, Bioengineering, or related Exp: 1 year |
Job duties include: Routine testing including in-process, release and stability testing of PCR, ELISA, and rapid test kits; Perform shipment checks, label inspections, and bacterial contamination testing; Identify and document process deviations as they occur in manufacturing and QC. | 2/17/2022 |
| 7585 | Indica Labs Remote, Field Applications Scientist - REMOTE: East Coast BS in biology or biomedical science Exp: 1 year |
Hybrid sales and technical position which provides Applications Support and some Sales Support in digital pathology and image analysis for Indica Labs, Inc’s HALO, HALO Link, and HALO AI platforms in a commercial, educational, or research environment. | 2/18/2022 |
| 7586 | Indica Labs Remote, Field Applications Scientist - REMOTE: West Coast BS in biology or biomedical science Exp: 1 year |
Hybrid sales and technical position which provides Applications Support and some Sales Support in digital pathology and image analysis for Indica Labs, Inc’s HALO, HALO Link, and HALO AI platforms in a commercial, educational, or research environment. | 2/18/2022 |
| 7587 | Genalyte San Diego, CA Process Development Associate BA/BS in Chemistry or Biological Sciences Exp: 0 - 2 years |
This is an entry level opportunity for a Process Development Associate to assist in assay development, manufacturing, and other team members in carrying out process development, technology transfer, Quality Control, manufacturing processes, and tasks involving a variety of laboratory methods, equipment and procedures. New grads are encouraged to apply. | 2/16/2022 |
| 7588 | Genomatica San Diego, CA Lab Technician, Process Development A Bachelor’s degree in chemistry, biology, molecular biology, biochemistry or related field. Exp: 0-6 months |
We are seeking a highly motivated and independent lab assistant to perform lab support duties and basic lab techniques. This is a part-time position. | 2/16/2022 |
| 7589 | Genomatica San Diego, CA Fermentation Associate I/II B.S. in chemical/biochemical engineering, bioengineering, molecular biology, microbiology, or biochemistry. Exp: 1-4 years |
We seek a highly motivated Fermentation Associate I/II for our Precision Fermentation Experimentation Team. This position experimentally generates high-quality fermentation data by applying optimal fermentor operating procedures, clearly communicating observations, working collaboratively to maximize experimental precision, and performing in-depth analysis of data generated. | 2/16/2022 |
| 7590 | Global Pharma Tek San Jose, CA Biochemist 1, Scientific Operations Requires a Bachelor’s degree in biological sciences Exp: 1 year |
Work with various functions such as Supply and Production Planning, Procurement, MDO, Manufacturing to coordinate and execute IVDR associated activities in San Jose Reagent Manufacturing to meet the BDB IVDR program timeline and deliverables. | 2/16/2022 |
| 7591 | Global Pharma Tek San Diego, CA Biochemist 1, Scientific Operations Minimum of BS or BA degree in Biology, Chemistry, Biochemistry, Molecular Biology, Immunology, or related discipline. Exp: 1 year |
Client is seeking a Biochemist I to work within a team that is manufacturing and developing new point-of-care assays for human in vitro diagnostic applications, using lateral-flow immunoassay technologies. | 2/16/2022 |
| 7592 | Globus Medical Methuen, MA Mechanical Engineer Bachelor’s Degree Exp: 1-5 years |
The Mechanical Engineer needs to have strong technical skills in mechanical engineering. Our Mechanical Engineers develop surgical robotics, x-ray imaging, and navigation systems by working with top surgeons and a cross-functional engineering teams. The position will be hands-on and the individual must be capable of creative and systematic product development with minimal supervision. | 2/16/2022 |
| 7593 | Globus Medical Audubon, PA Research Engineer Master’s Degree in the Sciences, Engineering, or Management fields Exp: 1-2 years’ |
The Research Engineer will be responsible for planning, coordination, successful execution, and publication of various research projects for spine surgeons, residents, and product development. In addition, this position will function in a cross-disciplinary environment and must have experience or be willing to be trained in image analysis, micro-CT, biomechanical principles, and orthopedic basic sciences. The Research Engineer must have strong self-starting qualities to independently manage coordination of multiple projects to ensure timely and successful completion. | 2/16/2022 |
| 7594 | Globus Medical Audubon, PA Laboratory Technologist Degree in Sciences or Engineering Exp: 1-2 years’ |
The Laboratory Technologist will be responsible for coordination and successful execution of various research projects for product development and marketing. This position will function in a cross-disciplinary environment to address lab requests in the areas of cell-culture, image analysis (scanning electron microscopy and micro-CT analysis), and animal study histology. The ideal candidate will have experience or be willing to be trained in image analysis or histology, but must possess training in basic cell culture techniques, sterile procedures, or other laboratory sciences. | 2/16/2022 |
| 7595 | Gossamer Bio San Diego, CA Contract Lab Assistant, R&D Ops (Part-Time) BA/BS Biology, Chemistry, Immunology, or other life science majors from an accredited college, or university. Junior and Senior year students are wel Exp: Entry Level |
This Part-Time Lab Assistant opportunity provides hands-on experience in lab operations, as well as the opportunity to gain exposure to the best research & development practices. Must be available to work 4 consecutive hours per day (M-F) between the hours of 8a-5pm. | 2/16/2022 |
| 7596 | Grand River Aseptic Manufacturing Grand Rapids, MI Mechanical Engineer Bachelor of Science degree in engineering, science, or technical discipline. Exp: 1+year |
Assist the Grand River Aseptic Manufacturing Facilities & Engineering and Operations departments by specializing in facility and utility optimization and providing subject matter expertise on mechanical systems. Run projects and oversee construction activities. Demonstrate, build, and enforce the best practices for all engineering projects and functions within the facilities. | 2/16/2022 |
| 7597 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Chemist I - 2nd or 3rd shift Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology) Exp: 1-3 years |
Support quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include but are not limited to providing general laboratory support for raw material, in-process, stability, and finished product testing. | 2/16/2022 |
| 7598 | Gregor Diagnostics Madison, WI Research Associate Master’s in Life Sciences or related field Exp: 1 years |
The Research Associate will be involved in Research and Development projects supporting and contributing to ongoing research projects. This role is primarily lab based and offers an opportunity to work directly on the prostate cancer screening test being developed at Gregor Diagnostics. The Research Associate role offers an opportunity to grow within a startup environment | 2/16/2022 |
| 7599 | Grifols Clayton, NC Assistant/Associate Biologist The Assistant level requires an AA or BS degree in medical technology/clinical laboratory science, or a BS degree in biology, chemistry or related fie Exp: 6-12 months |
The incumbent’s responsibilities include sample accessioning, sample preparation, reagent preparation, testing, result calculation, as well as quality control of assays and equipment. The incumbent will also support assay validation, method transfer, reagent and control qualification, and laboratory maintenance activities as assigned. Must be comfortable working with or around infectious material on a daily basis. Person must be able to work aseptically in a biological safety cabinet or laminar flow hood for several hours at a time. Candidates for the position must be proficient with using micropipettes and serological pipettes while making dilutions and serial dilutions. | 2/16/2022 |
| 7600 | Grifols Clayton, NC Raw Material Chemist (Assistant-Associate) AS/BS/BA degree in chemistry or related curriculum is required. Exp: six months |
Performs chemical testing of moderate to advanced complexity within a Quality Operations Laboratory in a safe, accurate, and efficient manner following established written procedures while maintaining complete and accurate records of the work and results. | 2/16/2022 |
| 7601 | Grifols Clayton, NC Assistant/Associate Biologist - QC Sterility AS/BS/BA degree in a life science field, medical technology, or related curriculum is required. Exp: 6 months |
The incumbent will perform biological testing of moderate to advanced complexity within the Quality Operations Laboratories in a safe, accurate, and efficient manner following established written procedures keeping complete and accurate records of the work and results. This position will be working primarily with the Closed Filtration System Sterility testing of Bulk and Final Container product in a class A/B aseptic environment according to established written procedures and following USP and EP regulations. | 2/16/2022 |
| 7602 | GRO Biosciences Cambridge, MA RA/Senior RA, Application Sciences BS/BA in biology, microbiology, biotechnology, synthetic biology, systems biology, biological engineering, or other related field. Exp: 1 year |
The individual selected for this position will work in Application Sciences and will facilitate early-stage product development. Regular activities will include planning and carrying out experiments throughout our product development pipeline, including cell line development, biomass generation, protein purification, protein characterization, and bioassays. | 2/16/2022 |
| 7603 | Glaxo Smith Kline Collegeville, PA Associate Analytical Scientist BS or MS in Chemistry or related scientific field. Exp: 1+ years’ |
As an Associate Analytical Scientist, you will progress analytical aspects of projects, utilizing your technical expertise as part of a product development and wider matrix teams. This role will provide YOU the opportunity to contribute to analytical development and to progress YOUR career. | 2/16/2022 |
| 7604 | Glaxo Smith Kline Rockville, MD Associate Microbiologist BA/BS in Science field Exp: 1 year |
GSK currently has an opening for an Associate Microbiologist in Rockville, MD. In this role, you’ll be providing routine QC Microbiology laboratory, with the purpose of meeting daily routine requirements as well as achieving goals established by the manager. | 2/16/2022 |
| 7605 | Glaxo Smith Kline Rockville, MD Associate QC Microbiologist Bachelor’s Degree in Biology OR Microbiology Exp: 1 year |
The job holder provides routine QC Microbiology laboratory, with the purpose of meeting daily routine requirements as well as achieving goals established by the manager. | 2/16/2022 |
| 7606 | Elixir Medical Corporation Milpitas, CA Manufacturing Engineer BS Mechanical or Manufacturing Engineering Exp: 0 years |
Responsibilities will include, but not be limited to: Contribute to cross-functional groups (Engineering, Quality, R&D, etc.) to resolve complex, cross-functional technical issues affecting production; Monitor metrics for product yield, cost and throughput; Contribute to efforts to improve in all three categories utilizing lean manufacturing principles; Design or improve manufacturing process equipment to improve quality and increase throughput. Experience in Medical Device a plus, including internships and/or coursework. Responsibilities will include, but not be limited to: Contribute to cross-functional groups (Engineering, Quality, R&D, etc.) to resolve complex, cross-functional technical issues affecting production | 2/10/2022 |
| 7607 | Elpis Biopharmaceuticals Lexington, MA Research Associate BS or MS in Biology, Biochemistry, Enzymology, Molecular Biology, Cell Biology, Immunology or related Exp: 0 years |
We are searching for passionate and highly motivated teammates to join our biology and functional assay group and contribute to our discovery platforms. We are searching for eager and driven research associates of different experience levels to analyze and screen newly discovered therapeutic molecules for biochemical, cellular and immunological function, as well as learn and apply new scientific techniques in our biologics and immune-modular programs. The candidate will also help explore and develop innovative technologies to advance our biologic projects | 2/10/2022 |
| 7608 | Encoded Therapeutics South San Francisco, CA Clinical Trial Assistant BS/BA in Life Sciences or related Exp: 1-2 years |
Reporting to the Clinical Program Manager, Clinical Operations, the Clinical Trial Assistant (CTA) will provide support to the clinical operations department and assist with the execution and maintenance of the clinical trials. The CTA will coordinate filing of documents into the Trial Master File (TMF), maintain various databases for clinical trial activity tracking and assist with contract and invoice management. | 2/10/2022 |
| 7609 | Ensoma Boston, MA Associate Scientist, Genomics BS or MS in Biology, Molecular Biology, Molecular Genetics, Biochemistry or related Exp: 1-3 years |
In this role, you will help develop novel in vivo viral-based gene therapies. You will initially be responsible for executing standard molecular biology-based workflows and work collaboratively between groups across the company. You will perform various NGS assays to characterize genomic structure of vectors and assess therapeutic efficacy and safety. You will partner with top-notch scientists and have an opportunity for accelerated technical skill development and diverse growth and learning opportunities. | 2/10/2022 |
| 7610 | Ensoma Boston, MA Associate Scientist/Senior Associate Scientist - In Vitro BS or MS in biological science Exp: 0+ years |
In this role you will help develop novel viral-based genomic medicine for hemoglobinopathies and other hematological disorders and work collaboratively with biology and platform development groups across the company. The successful candidate will be responsible for conducting experiments that functionally evaluate hematopoietic stem cells and lineages in vitro and ex-vivo. | 2/10/2022 |
| 7611 | Ensoma Boston, MA Associate Scientist/Senior Associate Scientist - Payload Engineering BS or MS in Molecular Biology, Synthetic biology, Molecular Genetics, Biochemistry, Immunology or related Exp: 1-3 years |
In this role, you will help develop novel in vivo based viral-based gene therapies. You will partner with top-notch scientists and have an opportunity for accelerated technical skill development and diverse growth and learning opportunities in the context of innovative therapeutics technology development utilizing a broad spectrum of gene editing and modification tools. Join us and be part of a company moving novel gene therapies into the clinic, revolutionizing the reach and access of the curative power of genomic medicines for patients with serious diseases. | 2/10/2022 |
| 7612 | Ensoma Boston, MA Associate/Senior Associate Scientist - In Vivo Biology BS or MS in biological science Exp: 0+ years |
In this role you will help develop novel viral-based genomic medicines for rare genetic disorders and work collaboratively within the company. The successful candidate will be responsible for conducting experiments that functionally evaluate hematopoietic stem cells (HSC) in vitro and in vivo. | 2/10/2022 |
| 7613 | Ensoma Boston, MA Research Associate Bioanalytical Assay Development MS in biology, molecular biology, biochemistry or related Exp: 0-3 years |
This is an ideal position for an individual with a background in biology, molecular biology, biochemistry or a related field who thrives in a team-oriented, fast-paced, and cross disciplinary biotech environment. The candidate will be an integral member of a small team of scientists across therapeutic discovery and translational sciences aiming to rapidly and pragmatically realize the potential of an emerging technology by supporting target engagement, PK/PD and tolerability studies in preclinical settings. | 2/10/2022 |
| 7614 | Exagen Vista, CA Laboratory Assistant BS in science Exp: 0 years |
The Laboratory Assistant is responsible for general laboratory tasks such as reagent preparation, inventory management, and operation of appropriate laboratory equipment under the supervision of a supervisor or delegate. | 2/10/2022 |
| 7615 | Exagen Vista, CA Data Scientist (Biostatistician) MS in biostatistics, bioinformatics, or related Exp: 0 years |
The Biostatistician designs and executes data mining, database queries, and statistical analysis relating to clinical studies, clinical laboratory data, and product development. Work with large datasets pertaining to clinical studies to design, develop, and perform statistical analysis for internal and external uses, including publications in peer-reviewed journals. | 2/10/2022 |
| 7616 | Exagen Vista, CA Research Associate I, Immunology BS in immunology, molecular biology, biochemistry or related Exp: 0 years |
The Research Associate I assists with the development of new assays for diagnostics and research projects, through various phases of inception, planning and transfer to the clinical lab. | 2/10/2022 |
| 7617 | EyeCro Oklahoma City, OK Research Technician I BS in chemical, biological, or physical sciences Exp: 0 years |
EyeCRO, LLC, an ocular pharmaceutical and contract research company is seeking highly motivated individuals for a full-time research position. This person will be responsible for participating in a wide variety of laboratory-based activities related to molecular/cell biology, biochemistry, and in-vivo experimentation. | 2/10/2022 |
| 7618 | Facet Medical Technologies Atlanta, GA Quality Engineer BS or MS in engineering or science Exp: 1-3 years |
Plans and directs activities concerned with development, application, and maintenance of quality processes, materials, and products. Additionally, responsible for investigation manufacturing and customer nonconformance’s, determining root causes and corrective actions, reviewing and approving protocols and final reports and developing product specifications and sampling plans. | 2/10/2022 |
| 7619 | Fate Therapeutics San Diego, CA Associate Scientist/ Senior Research Associate (iPSC-derived CAR-T) BS or MS in immunology, cell biology, biochemistry, molecular biology, or related Exp: 0+ years |
Fate Therapeutics is seeking an experienced and highly motivated Associate Scientist or Senior Research Associate with cell-based assay development expertise to assist in functional characterization of Fate’s next generation iPSC-derived CAR-T cell cancer immunotherapies. The successful candidate will be responsible for performing assays to identify and evaluate functional attributes of Fate’s T cell products. The ideal candidates have prior research/discovery experience and enjoy working in a team-based environment. | 2/11/2022 |
| 7620 | Fate Therapeutics San Diego, CA Research Associate I, MSAT BS or MS in Biological sciences, Biomedical Eng., Chemical Eng., Process Science, or related Exp: 1-2 years |
The successful candidate will join a multidisciplinary team evaluating new technologies and developing novel processes for the scaled-up manufacturing of cellular immune therapies from human induced pluripotent stem cells (iPSC). The candidate will lead and support projects in the Downstream MSAT team to develop scaled-up or scaled-down culture, differentiation, purification, and characterization methods for iPSC-derived cellular therapy products. This position will actively support laboratory operations by coordinating the inventory, purchase and aliquoting of key reagents. | 2/11/2022 |
| 7621 | Ferring Parsippany, NJ Specialist, Process Exellence BS in Science or Engineering Exp: 0-2 years |
The purpose of the role is to support the Process Excellence group complete objectives. The role will support technology transfer projects and provide support for routine activities (deviations, investigations, data analysis). | 2/11/2022 |
| 7622 | Ferring Roseville, MN Quality Control Lab Technician BS in science Exp: 1 year |
The purpose of the Quality Control (QC) Lab Technician is to support the daily activities of the QC Laboratory. This includes but not limited to donor source material inspections, review of send out testing, laboratory testing preparations. | 2/11/2022 |
| 7623 | Flowonix Mount Olive, NJ Clinical Engineer MS in Engineering Exp: MS: 0 years, BS: 2 years |
Under the supervision of the Director, Sales Training and Development, the Clinical Engineer (CE) is responsible for providing support to the field through engineering and product knowledge. The Clinical Engineer is responsible for documenting and resolving technical issues received from customers and field representatives as well as coordinating and supporting multiple cross-functional in-house teams including sales education and training. | 2/11/2022 |
| 7624 | Foghorn Therapeutics Cambridge, MA Research Associate, Biochemistry and Biophysics BS or MS in Biochemistry, Biophysics, or related Exp: 0-3 years |
As a member of our Drug Discovery team the candidate will have an opportunity to employ various biochemical and biophysical assay technologies in mechanism of action studies, screening and hit validation. The job would involve designing, developing, and troubleshooting in vitro biochemical and biophysical assays for both protein-protein and small molecule-protein interactions. | 2/11/2022 |
| 7625 | Foghorn Therapeutics Cambridge, MA Research Associate, Biology & Cellular Assays BS or MS in Biology or Biochemistry Exp: 1-2 years |
The candidate will play a key role in oncology drug discovery and translational biology research. The candidate must have demonstrated proficiency in the development of cell-based assays and use of standard molecular and cellular biology techniques. The candidate should have a track record of applying sound scientific judgement to answer critical questions, as well as a proven ability to design and implement thoughtful and well-controlled experiments. | 2/11/2022 |
| 7626 | Frontier Medicines South San Francisco, CA Coumpound Management Technician BS/BA in Life Sciences or related Exp: 0 years |
Frontier Medicines is seeking a highly motivated individual for the position of Compound Management Technician. The successful candidate will be accountable for storage, retrieval and distribution of compounds for biological assays as well as chemical building blocks for compound synthesis and QC. | 2/11/2022 |
| 7627 | Frontier Medicines Boston, MA Research Associate, Bioinformatics MS in Bioinformatics, Computational Biology, Genomics, Computer Science, Physics, Statistics, Data Science or similar Exp: 0 years |
The successful candidate will play a vital role in developing algorithms and analytical strategies to create value from our unique data coming out our chemoproteomics platform as well as more traditional large-scale data such as genomics, proteomics, metabolomics, phenotypic profiling. | 2/11/2022 |
| 7628 | FYR Diagnostics Missoula, MT Clinical Laboratory Technician in Training BS or MS in a health or science related field Exp: 0 years |
FYR Diagnostics is currently seeking scientists interested in obtaining Clinical Lab Technicians to perform high-complexity molecular diagnostic tests in our CLIA laboratory. This training is paid. | 2/11/2022 |
| 7629 | Gameto New York, NY Data Scientist (Bioinformatician) MS in Computer Science, Bioinformatics, Engineering, Math, Statistics, Physics, or related Exp: 0 years |
Gameto is looking for exceptional candidates to join our team, either remotely or locally in New York City. The successful candidate will join an interdisciplinary team of computational biologists, engineers, and stem cell biologists, who are working to transform the reproductive longevity space, by leveraging the advances of cellular reprogramming to make menopause optional and address aging through the lens of the ovary. A working knowledge of high-throughput DNA and RNA sequencing is required, along with a passion for playing an essential role in the development of transformative therapies. | 2/11/2022 |
| 7630 | Garuda Therapeutics Cambridge, MA Scientist/Associate Scientist-R&D BS or MS in molecular biology, cell biology, or related Exp: 1-2 years |
Garuda Therapeutics is seeking highly motivated scientists/research associates to join its growing team. Successful candidates will be integral in developing stem cell-derived therapies for hematologic disorders. The position requires enthusiasm, dedication, attention to detail, and teamwork ability. The position will be located in Natick, MA or Cambridge, MA. | 2/11/2022 |
| 7631 | Decipher Biosciences San Diego, CA Research Associate I, Assay Development BS Biological Science or related Exp: 1-2 years |
The Research Associate I will support the Assay Development team at Decipher Biosciences; assisting in research, development, and optimization of genomic assays, and supporting general laboratory maintenance and document control. Other responsibilities might be applied as needed. | 2/8/2022 |
| 7632 | Deepcell Menlo Park, CA R&D Engineering Associate BS Engineering (Physics, Electrical Eng., Bioengineering, or Mechanical Eng.) Exp: 0-1 years |
Responsibilties: Conducts experiments on research instruments and collects data; Implements improvements to optical assemblies on instruments; Statistical analysis of data collected; Monitors instrument performance, identifying failures and documenting them; Implements process improvement tasks and helps updating related SOPs; Assists in troubleshooting hardware issues that arise, documenting these issues in FMEA; Identifies ways to eliminate recurring issues | 2/8/2022 |
| 7633 | Deepcell Menlo Park, CA Research Associate, Biology BS or MS bioengineering, molecular biology, cell biology, genetics, or similar Exp: BS: 1+ years; MS: 0 years |
We are looking for multiple research associates to join the biology team and help us to unlock the power of cell morphology and connect the genome to the patient. Responsibilities include: Assist in designing and executing experiments on the Deepcell R&D platforms; Inventory, accessioning, and tracking of incoming samples into the lab; Perform cell culture, cell maintenance, and sample processing protocols; Execute standard molecular and cell biology protocols (e.g. FACS, PCR, qPCR, DNA library prep, sequencing on in-house sequencers); Follow good laboratory practices including taking meticulous notes for experiment documentation; Develop clear workflows and SOPs, and refine existing ones; Communicate effectively and coordinate tasks with cross-disciplinary teams; Perform routine laboratory maintenance activities, including ordering, receiving, and cataloging supplies, as well as maintaining consumable inventories | 2/8/2022 |
| 7634 | Demetrix Berkeley, CA Media Prep & Lab Services Technician BS or Associate's Exp: 0 years |
This position will be part of the Lab Services team and will be playing a key role within the R&D group by maintaining reagents, media and glassware stocks for the strain and fermentation engineers. In this role you will assist with inventory management, waste stream management, freezer management, glass washing and autoclaving, equipment moves, and will also have a chance to assist in creating and improving current protocols. Demetrix is a diverse mix of talented people committed to building an environment where everyone feels welcome and is able to do impactful, meaningful work. | 2/8/2022 |
| 7635 | Denison Pharmaceuticals Lincoln, RI Analytical Data Review Specialist BS Chemistry Exp: 0 years |
The Analytical Data Review Specialist requires an analytical chemistry background and experience with Good Manufacturing practices (cGMP). The Analytical Data Review Specialist candidate must also obtain Quality Control Laboratory testing in order to be considered for this position. | 2/8/2022 |
| 7636 | Denison Pharmaceuticals Lincoln, RI Quality Specialist BS in any science field Exp: 1-3 years |
Denison Pharmaceuticals is a leading provider of turnkey formulation, manufacturing and packaging solutions for the OTC, Cosmetic, Homeopathic and Pharmaceutical markets. Products include liquids, creams, lotions, gels, and ointments. The successful candidate for the position of a Quality Specialist shall be fully capable of performing these job functions: Review/Approval of all facility documentation; OOS, Deviations, Investigations, Change Controls, CAPA’s; Oversight of Quality training program in QMS; Perform QA On-The-Floor program to review production documentation; Writing/Revising SOP’s when needed; Ensuring regulatory compliance throughout facility; Investigation of customer complaints; Assist in gathering Key Performance Indicators (KPI’s) for quality related activities | 2/8/2022 |
| 7637 | DewPointX Boston, MA Research Assoicate - Screening & Automation BS or MS in biochemistry, cell biology, biotechnology, or related Exp: 1+ years |
We are looking for a creative, energetic individual to join our team as a screening and automation Research Associate/Sr. Research Associate supporting high content/ high throughput assays and instrumentation for multiple disease areas. The successful candidate will be highly skilled in cell-based assay development and validation, in the context of high throughput screens. | 2/9/2022 |
| 7638 | DewPointX Boston, MA Research Assoicate - Rare Diseases BS or MS in biochemistry, molecular biology, cell biology, or related Exp: 1+ years |
We are searching for a creative, experienced, and independent Research Associate or Senior Research Associate to join the drug discovery efforts in our rare disease therapeutic area. You will contribute to a team developing and executing cellular assays to characterize disease-relevant condensates and to discover novel therapeutics. | 2/9/2022 |
| 7639 | Diabetomics Hillsboro, OR Research Assistant/Associate in Product Development BA/BS in a relevant biological science Exp: 1-2 years |
Applies knowledge of scientific principles and concepts to the design, development, and execution of Product Development experiments. Demonstrates technical proficiency, scientific creativity, collaboration with others and can work independently; Under guidance of senior personnel, designs and conducts research and/or product development, assay optimization and scale-up tasks and experiments based on the needs of the group; Ensures compliance with and helps to implement the requirements of working in a regulated environment to assure adherence to various requirements, including Design Control, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP); Helps to coordinate general laboratory tasks such as reagent preparation, inventory and organization of work. | 2/9/2022 |
| 7640 | Dicerna Lexington, MA Research Associate - Translational Biology BS or MS in Biology. Pharmacology, or related Exp: 1-3 years |
We are seeking a highly skilled research associate to lead mechanism of action and pharmacology studies on Dicerna’s GalXC therapeutics. Major responsibilities include conducting in vivo studies on our pre-clinical and clinical candidates and conducting hands-on research. You will apply your expertise on animal dosing and surgery and deep understanding of the molecular and cellular biology to study liver diseases and play an important role in all phases of drug discovery and clinical development at Dicerna. | 2/9/2022 |
| 7641 | Dicerna Lexington, MA Cheminformatics Associate, Research Chemistry BA/BS in Computer Science, Math, Statistics, Chemistry, Physics, Informatics Exp: 1+ years |
We are seeking a Cheminformatics Associate to help support Dicerna’s research scientists with our in-house software and workflows. This position is an ideal fit for a candidate who has a good understanding of both software development and scientific research. It offers plenty of opportunity for growth within the organization over time. Minimum 1+ year experience in either industry or academia. | 2/9/2022 |
| 7642 | DNA Diagnostics Center Fairfield, OH Laboratory Technologist (2nd/3rd shift) BS in Biological Science Exp: 1-2 years |
The Lab Technologist is responsible for the execution of a broad range of bench test procedures used in raw material qualification, and testing. In this position, you will work in a fast paced, customer focused, and challenging environment. Laboratory technologists assist with the receiving, labeling, testing and analyzing of samples in a sterile environment. They assist in the design and execution of laboratory testing according to standard procedures, as well as maintain accurate computer records of the process and results. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work as well as ability to work overtime and off-schedule days as needed. | 2/9/2022 |
| 7643 | DxTerity Los Angeles, CA Research Associate BS or MS in Biochemistry, Molecular Biology, or related Exp: 1-3 years |
DxTerity, a patient-centric genomics company located in Los Angeles, CA is looking to hire a Research Associate to join our Research and Product Development team. Responsibilities include: development of molecular diagnostic test kits, reagents and procedures in a team environment. Perform experiments independently after receiving general direction from supervisor. Make detailed observations, analyzes data and interpret results. Prepare technical reports, summaries, protocols and quantitative analyses. Maintain and develop skills in molecular biology and company technology through reading of internal reports and scientific literature. Support the achievement of project objectives and time schedules while meeting ISO and FDA regulatory and design control requirements. | 2/9/2022 |
| 7644 | DxTerity Los Angeles, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations BS or MS in chemical, biological or clinical laboratory science, or medical technology Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 2/9/2022 |
| 7645 | Elevar Therapeutics Remote, Trial Master File Specialist, Clinical Operations BS in science or health-related field Exp: 1-3 years |
The TMF Specialist is responsible for supporting a high quality TMF, performing quality checks, archival and retrieval of records for the Trial Master Files (TMF). Responsibilities include but are not limited to driving and overseeing successful completion of all TMF deliverables. This is a remote-based position. | 2/9/2022 |
| 7646 | Steripharma Syracuse, NY Microbiology Analyst, 2nd Shift, Pharma A Bachelor’s degree from a regionally accredited institution in science or related field Exp: 1 year |
Performs a variety of micro testing on finished products, raw materials, and components | 3-Jan-22 |
| 7647 | Steripharma Syracuse, NY Production Technician - All Shifts, Pharma A Bachelor’s degree from a regionally accredited institution in science or related field Exp: 1 year |
Operates all assigned equipment appropriately and per established methods and procedures, to include set up, operation and cleaning of equipment and parts, confirming configurations are correct, checking for leaks or other abnormalities or anomalies, ensu | 3-Jan-22 |
| 7648 | Sterling Germantown, WI Production Chemist B.S. Degree (Science-based preferred) or High School diploma with equivalent experience Exp: |
Synthesizes, isolates and purifies products and intermediates by using standard chemistry techniques from gram to tonne scale. | 3-Jan-22 |
| 7649 | Straumann Gothenburg, Sw QC analyst Biomedical analyst, college education in chemistry, biochemistry or similar Exp: 0-1, recent graduate |
Work most of the time with laboratory work but also some office work such as writing different quality documents | 3-Jan-22 |
| 7650 | Surmodics Eden Prairie, MN Associate Scientist Bachelor’s degree in Chemistry or related field preferred Exp: 1 year |
Executes hands-on work per trained procedures under the direction of the line supervisor | 3-Jan-22 |
| 7651 | Surmodics Eden Prairie, MN Associate QC Scientist B.S. or B.A. degree in chemistry, biology or appropriate discipline Exp: 1 year |
Prepare and analyze samples according to established test methods | 3-Jan-22 |
| 7652 | Ethos Laboratories Newport, KY PCR Specialist Master of Science in Life Science, Pharmacology, Toxicology, Biology, Physics, Chemistry, or similar analytical science field. Exp: 0+ years |
The PCR Specialist is responsible for sample preparation, machine operation, and running samples for a standard PCR workflow. This person will ensure that samples are prepared according to laboratory SOPs and that the correct workflow for PCR is adhered to. This person will also be responsible for loading and operating standard PCR equipment such as extraction instruments, thermal cycling instruments, and PCR instruments. The PCR Specialist is responsible for sample preparation, machine operation, and running samples for a standard PCR workflow. This person will ensure that samples are prepared according to laboratory SOPs and that the correct workflow for PCR is adhered to. This person will also be responsible for loading and operating standard PCR equipment such as extraction instruments, thermal cycling instruments, and PCR instruments. | 12/6/2021 |
| 7653 | Eurofins Viracor BioPharma Services San Diego, CA Biochemist Research Associate Bachelor degree in biology, biochemistry, molecular & cell biology, chemistry, life sciences, or other related degree concentration Exp: 1 years |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a Biochemist Research Associate to support our Professional Scientific Services group in San Diego, CA. | 12/6/2021 |
| 7654 | Eurofins Viracor BioPharma Services Madison, WI Food Chemistry Testing Bachelor's degree in chemistry, biology or other related degree concentration, or equivalent directly-related experience Exp: Entry-level |
We are seeking immediate talent to support our clients to help make our world a safer place. We are seeking talent at all experience levels, from entry-level undergraduate to senior scientists with a life science degree in chemistry, biology or related sciences. Additional training will be provided. Analytical testing of foods, supplements, ingredients, and packaging. Includes work on: accurate nutrition labels, creating safe products and supply chains, and assisting with compliance with FDA and international regulatory agencies. We are seeking immediate talent to support our clients to help make our world a safer place. We are seeking talent at all experience levels, from entry-level undergraduate to senior scientists with a life science degree in chemistry, biology or related sciences. Additional training will be provided. Analytical testing of foods, supplements, ingredients, and packaging. Includes work on: accurate nutrition labels, creating safe products and supply chains, and assisting with compliance with FDA and international regulatory agencies. | 12/6/2021 |
| 7655 | Eurofins Viracor BioPharma Services University Park, IL Organic Extractions Analyst/Scientist - Environmental Laboratory (Entry-level Evening Shift)- Eurofins TestAmerica - University Park, IL BS or BA in chemistry or related field preferred but not necessary Exp: Entry-level |
The Analyst I Organic Extractions prepare and analyze environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins Eurofins Eurofins TestAmerica’s Quality Assurance programs and SOP’s. | 12/6/2021 |
| 7656 | Eurofins Viracor BioPharma Services Cambridge, MA Research Associate BS or MS degree in Cell and Molecular Biology, Biochemistry, Pharmaceutical, or other biological/analytical discipline Exp: BS: 0-2 years ; MS: 0+ years |
Supports viral vector process development by providing analytical testing on DNA, ELISA, cell based platform within agreed upon turn-around Demonstrate good understanding of ongoing programs and data generated in relation to the program Troubleshoots issues as needed with supervisionSupports viral vector process development by providing analytical testing on DNA, ELISA, cell based platform within agreed upon turn-around Demonstrate good understanding of ongoing programs and data generated in relation to the program Troubleshoots issues as needed with supervision | 12/6/2021 |
| 7657 | Eurofins Viracor BioPharma Services Evesham, NJ Microbiology Laboratory Technician - Eurofins EMLab P&K - Marlton, NJ BS or BA in a closely related science Exp: 1 year |
The Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and standard operating procedures, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 12/6/2021 |
| 7658 | Eurofins Viracor BioPharma Services Irvine, CA Bacteria Analyst - Eurofins EMLab P&K - Irvine, CA Bachelor’s degree in microbiology, biology, geology or a closely related science preferred. 8 units of Microbiology courses preferred. Exp: 1+ years |
Eurofins EMLab P&K is searching for an experienced Bacteria Analyst in Irvine, CA The Analyst primarily performs bacterial culture and screening analysis of environmental samples. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and enters laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation.Eurofins EMLab P&K is searching for an experienced Bacteria Analyst in Irvine, CA The Analyst primarily performs bacterial culture and screening analysis of environmental samples. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and enters laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 12/6/2021 |
| 7659 | Evolve BioSystems Davis, CA QUALITY ASSOCIATE OR SENIOR QUALITY ASSOCIATE, QUALITY AND FOOD SAFETY BSc degree Exp: 1 to 3 years |
The Research Associate will support the development and quality of Evolve’s growing portfolio of proprietary microbiome products. This person will leverage their skills in microbiology, chemistry, food science, or related areas to influence both current and future work streams within the company. The successful candidate will thrive in a fast-paced, entrepreneurial environment at an early-stage company. The position is based in Davis, CA, and reports to the Quality Manager. | 12/8/2021 |
| 7660 | Exosome Diagnostics [Bio -Techne] Minneapolis, MN Research Associate, Conjugation Bachelor’s degree in chemistry, biological sciences or equivalent (chemistry or biochemistry preferred) required Exp: 0 to 2 years |
This position is responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel. | 12/8/2021 |
| 7661 | Exosome Diagnostics [Bio -Techne] Minneapolis, MN Research Associate Bachelor’s degree in a science related field; Or Masters degree in a science related field Exp: 0-3 years |
The Bioassay Development group is seeking a Senior Research Associate (RA) with experience in cell-based assays, ELISAs and Plate-based testing. The successful candidate will primarily be responsible for the development and qualification of assays for the characterization and identity, purity, and strength assessment of recombinant proteins. | 12/8/2021 |
| 7662 | Exosome Diagnostics [Bio -Techne] Minneapolis, MN Research Associate, Quality Control Bachelor’s degree in a related field Exp: up to 3 years |
This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 12/8/2021 |
| 7663 | Exosome Diagnostics [Bio -Techne] Minneapolis, MN Research Associate, Array Manufacturing bachelor’s degree in chemistry, biological sciences or equivalent Exp: 0 to 2 years |
This position is responsible for preparing intermediate antibody cocktails for various product lines, participating in Proteome Profiler Array printing, and performing in-process Array component testing. In addition, this position is responsible for BioRobotics MicroGrid II MicroArrayer start up and/or take-down, basic maintenance and troubleshooting. | 12/8/2021 |
| 7664 | Exosome Diagnostics [Bio -Techne] San Jose, CA Research Associate Bachelor's Degree in biotechnology, biochemistry, or related field Exp: up to 3 years |
The Applications Science team is seeking a highly motivated Research Associate to join their ranks! In this position, you will work daily with innovative analytical platforms alongside our scientists to contribute exciting data for scientific collateral and custom projects. As part of this team, the Research Associate is also expected to join support efforts to put out fires (escalations) via instrument testing, assay testing, etc. | 12/8/2021 |
| 7665 | Exosome Diagnostics [Bio -Techne] Minneapolis, CA Research Associate Protein Purification Development Bachelor’s degree in Biology or related field Exp: up to 5 years |
We seek a highly motivated and creative individual to join our protein purification development team. Our team is responsible for the development of Bio-Techne's various product lines, with a focus on the high-quality recombinant protein products. You will participate in the development and optimization of protein purification procedures for recombinant proteins expressed in various cell lines (E. coli, baculovirus, and mammalian). In addition, you will also assist with initial, small-scale production for release of newly developed proteins and redevelopment of existing products to help advance Bio-Techne's evolving portfolio. This is a great opportunity to gain experience with cutting-edge biotech development/manufacturing processes & practices while working in a collaborative laboratory environment.We seek a highly motivated and creative individual to join our protein purification development team. Our team is responsible for the development of Bio-Techne's various product lines, with a focus on the high-quality recombinant protein products. You will participate in the development and optimization of protein purification procedures for recombinant proteins expressed in various cell lines (E. coli, baculovirus, and mammalian). In addition, you will also assist with initial, small-scale production for release of newly developed proteins and redevelopment of existing products to help advance Bio-Techne's evolving portfolio. This is a great opportunity to gain experience with cutting-edge biotech development/manufacturing processes & practices while working in a collaborative laboratory environment. | 12/8/2021 |
| 7666 | Forge Biologics Columbus, OH GMP Associate (multiple positions) Bachelor’s Degree (B.A. or B.S.) in scientific-related field or engineering Exp: 1-2 years’ |
We are currently seeking a GMP Associate to join the Forge Biologics team. This is an exciting opportunity to contribute to and lead efforts in the execution of manufacturing life changing gene therapies for human use. The candidate will participate in GMP manufacturing campaigns and provide hands-on support for new technologies and systems in our GMP manufacturing facility. The ideal candidate will be skilled in technical problem-solving and laboratory techniques to support our growth in the Gene Therapy sector. The GMP Associate provides manufacturing and operational expertise for the Forge GMP facility in Grove City, OH. This will include technical writing, routine testing, and all other associated activities. The GMP Associate responsibilities include, but are not limited to; training, sampling, manufacturing activities, method qualification/validations, investigations, and cleaning support. Additional responsibilities include adherence to all GMP requirements, a basic understanding of FDA/EMEA regulations, and effective interactions/communication with Operations Management. The GMP Associate may also support the Operations management team for activities related to interviewing and training of employees, compliance with GMP, and identifying and implementing corrective and preventive actions. | 12/8/2021 |
| 7667 | Global Blood Therapeutics South San Francisco, CA Research Associate II, Translational Biology BA/BS in biochemistry, molecular biology or equivalent discipline Exp: 1-3 years |
The Biology Department at Global Blood Therapeutics is looking for a qualified Research Associate with experience troubleshooting and protocol development experience. This position will be primarily responsible for supporting critical instruments, supporting internal animal studies across pipeline programs, and writing protocols around instrument care. The applicant will also provide logistics and troubleshooting support for animal and clinical studies conducted externally. An ideal candidate will be detail-oriented, organized, and comfortable working both independently and within a team. | 12/16/2021 |
| 7668 | DVC LLC [General Dynamics Information Technology] Silver Spring, MD Research Assistant BS in Biology, Microbiology, Medical Technology or related field Exp: 1+ years |
GDIT is hiring a Research Assistant to join our team in support of the Naval Medical Research Center Infectious Disease Directorate (NMRC IDD) activities in Silver Spring, MD. The mission of the NMRC IDD is to research and develop countermeasures to protect Navy and Marine Corps personnel against infectious agents of military importance. This position would provide support to the NMRC IDD Wound Infections Department by carrying out laboratory research procedures for working with multidrug resistant bacteria causing traumatic wound infections. | 12/16/2021 |
| 7669 | DVC LLC [General Dynamics Information Technology] Silver Spring, MD Research Technician - Vector Biology BS in Biological Sciences Exp: 1-2 years |
GDIT is seeking a research assistant to provide technical support services necessary to perform entomological research in support of the Entomology Branch at the Walter Reed Army Institute of Research (WRAIR). | 12/16/2021 |
| 7670 | DVC LLC [General Dynamics Information Technology] San Diego, CA Molecular Laboratory Technician Associates or Bachelors degree in a Science related field Exp: 0-2+ years |
GDIT is seeking a Molecular Laboratory Technician in support of the Naval Health Research Center (NHRC) Infectious Disease Field Surveillance and Laboratory Research Services. As the Navy hub for the Armed Forces Health Surveillance Center the NHRC Operational Infectious Diseases Directorate conducts on-going laboratory-based surveillance of US military populations in unique environments to quantify and study the etiology of infectious illnesses. | 12/16/2021 |
| 7671 | Codexis Redwood City, CA Associate Engineer/Research Assistant Downstream Bioprocess Development Bachelor’s degree in Biochemistry, Biological Science, Chemical Engineering, or related discipline Exp: 0-3 years |
To help us meet out goals we are hiring an Associate Engineer/Research Assistant to join our Downstream Bioprocess Development Team. In this role you will design, perform, and analyze DSP experiments to extablish, understand and optimize purification processes for life science enzymes that are used in diagnostic and other molecular biology applications. | 11/30/2021 |
| 7672 | Codexis Redwood City, CA Process Engineer I, Downstream Bioprocess Master’s degree in Biochemistry, Biological Science, Chemical Engineering or related discipline Exp: 0-3 years |
We are looking to hire a Process Engineer/Research Associate to join our Downstream Bioprocess Development Team. In this role you will design, perform, and analyze experiments to establish, understand, and optimize purification processes. You will also play a key role to support selection of lead therapeutic candidates for the treatment of rare genetic disorders. | 11/30/2021 |
| 7673 | Codexis Redwood City, CA Research Assistant I/II, Quality Control BS in Analytical Chemistry, Biochemistry or Biological Sciences or equivalent Exp: 1-3 years |
We are currently seeking a highly motivated and detail-oriented Quality Control Research Assistant to join our Quality Control Team. As part of this collaborative team you will oversee day-to-day QC operations and analyses of biocatalysts (enzymes) to contribute to the release of commercial products as well as support analytical development for cross functional teams. | 11/30/2021 |
| 7674 | Codexis Redwood City, CA Research Assistant, Automation & Analytics BS or equivalent in Life Science Exp: 1 ~ 3 years |
We are looking to hire Research Assistant (with focus on high-throughput, Automated Experiments) to join our Automation Engineering group within the Automation & Analytical Sciences department. | 11/30/2021 |
| 7675 | Codexis Redwood City, CA Research Assistant, Media Prep Bachelor’s Degree in Biology, Biochemistry, Biotechnology, Molecular Biology or related field. Exp: Entry Level |
We are looking to hire a highly motivated Research Assistant/Associate to broadly support the research organization. As part of this collaborative team within the Automation Operations Group, you will prepare media, reagents and glassware to support the ongoing needs of scientists in the R&D group. | 11/30/2021 |
| 7676 | Codexis Redwood City, CA Research Assistant/Associate Automation Operations Bachelor’s degree or equivalent recognized qualification Exp: 1 - 3 years |
We are looking to hire a highly motivated Research Assistant/Associate to join our Automation Operations team. Working in this team setting, you would contribute the efforts of the high throughput protein expression laboratory to support the development and discovery of novel enzymes. This lab operates seven days a week to support research and development efforts. | 11/30/2021 |
| 7677 | Coherus Biosciences Camarillo, CA Temporary Research Associate Requires a Bachelor’s degree in chemistry, biology, or biochemistry. Exp: 1+ years |
Performing research and development experiments for projects and products in collaboration with others. Execute a range of biophysical and biochemical assays and characterization work. Make detailed observations, maintain laboratory notebooks, analyze data and interpret results. Interact with other staff members on analytical methods development and execution of specific analytical assays. | 11/30/2021 |
| 7678 | CoImmune Durham, NC Production Associate I, Cell Base Therapies Requires Associate Degree; May have a Bachelors degree; however not required. Exp: 0-2 years’ |
The individual will work under close supervision to conduct cGMP manufacturing of a cell-based product. This includes validation and development runs under cGMP and assistance in technology transfer of novel products. All activities will be performed in a cGMP-compliant environment. | 11/30/2021 |
| 7679 | CoreRX Inc. Clearwater, FL MICROBIOLOGIST BS or BA in microbiology or related field is preferred Exp: 1-2 years |
Conduct facility environmental testing using particulate counter and microbial air sampler Performs necessary microbial testing using aseptic technique Communicate environmental issues to operations and quality | 11/30/2021 |
| 7680 | Contract Pharmacal Hauppauge, NY SCIENTIST I; AR&D Bachelor’s or Master’s degree in chemistry or analytical chemistry Exp: 1-2 years |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. | 12/1/2021 |
| 7681 | Crown Bioscience San Diego, CA Research Associate I - Biomarker & Diagnostic Tech Bachelor of Science degree or above in biotechnology, cell biology, immunology, oncology or other related disciplines Exp: one year |
The purpose of the Research Associate I position is to provide support on biomarker discovery studies to meet company's goals, objectives and quality standards. | 12/1/2021 |
| 7682 | Crown Bioscience San Diego, CA Research Associate II, In Vivo Oncology Bachelor’s Degree in a scientific discipline Exp: One year |
In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 12/01/2021 |
| 7683 | Crown Bioscience San Diego, CA Research Associate I - Cell Support Bachelor's degree in Biology, Biochemistry or related area Exp: 1-2 years |
The purpose of the Cell Support - Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 12/01/2021 |
| 7684 | Crown Bioscience San Diego, CA Research Associate I, In Vivo Oncology Bachelor’s Degree in a scientific discipline Exp: One year |
In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 12/02/2021 |
| 7685 | Crown Bioscience San Diego, CA Research Associate I - Cancer Biology & Immunology Requires a Bachelor's degree in Biology, Biotechnology or other relevant area of scientific discipline Exp: 1‐ 2 years |
The purpose of the Cancer Biology Immunology Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 12/02/2021 |
| 7686 | CSL Behring [Seqirus Inc] Holly Springs, NC Associate I/II/III, Manufacturing (Fill Finish) Night Shift Bachelor’s degree in science or engineering preferred Exp: 1 year |
The incumbent will be a shop floor employee in the Seqirus manufacturing organization. The incumbent will provide (be trained in) the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant, efficient, and cost effective manner. *Schedule – Nights - 2,2,3 – 6pm-6am *Every other weekend off *Level will be determined by years of experience | 12/02/2021 |
| 7687 | CSL Behring [Seqirus Inc] Holly Springs, NC Associate I/II/III, Manufacturing (Small Scale Filling) Bachelor’s degree in science or engineering preferred. Exp: 1 year |
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (be trained in) the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant, efficient, and cost effective manner. Day shift role - M-F -8am-5pm Level will be determined by years of experience | 12/02/2021 |
| 7688 | Cygnal Therapeutics Cambridge, MA Research Associate/Sr. Research Associate, Platform BS/MS in neurobiology, immunology, cell biology, or related discipline Exp: 0-5 years |
Cygnal is seeking a Research Associate/ Sr. Research Associate to join our Platform Biology team, working closely with our scientists across multiple backgrounds including neuroscience, immunology and neuroimmunology to develop and perform assays and identify targets and therapeutics. The candidate must be highly motivated, creative, goal oriented, and willing to work in a highly dynamic and fast-paced entrepreneurial environment | 12/02/2021 |
| 7689 | Cyprotex Watertown, MA Research Associate and/or Research Assistant - Toxicology BS/ MS in a relevant bio scientific discipline Exp: 0-2 years’ |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays | 12/02/2021 |
| 7690 | Cyprotex [Evotek] Boston, MA Laboratory Technician - Sample Management BS or equivalent with scientific discipline Exp: 1-2 years’ |
Evotec (US) Inc. has a Sample Management Laboratory Technician position open, located at a sample management department within a large pharmaceutical company in Boston MA. Major Job responsibilities will be manual solid sample weighing and solubilization of the solid samples using an automated liquid handler. The position requires a highly motivated individual, able to work independently, and as part of a team, to ensure successful project support. This role will be expected to have increased understanding of Sample Management workflows, set forth SOPs, etc. | 12/02/2021 |
| 7691 | Cytovance Biologics Oklahoma City, OK ANALYTICAL DEVELOPMENT ASSOCIATE I AD Associate I - BS in a life science field; AD Associate II - MS in a life science field Exp: 1+ years |
The AD Associate I/II position develops, optimizes, and qualifies analytical methods for biopharmaceutical products. The associate also supports drug development departments, such as Purification Department and Cell Culture Department, by performing analytical testing. | 12/02/2021 |
| 7692 | Cytovance Biologics Oklahoma City, OK PROCESS DEVELOPMENT ASSOCIATE Bachelor’s degree in a life science field Exp: 0-3 years |
The Process Development Associate I conducts laboratory experiments as part of development and/or demonstration of processes related to purification of biopharmaceutical products. The Associate also participates in activities related to the maintenance and upkeep of the Process Development Lab. | 12/03/2021 |
| 7693 | Demetrix Berkeley, CA Process Engineer Bachelor of Science degree (biological system or chemical engineering, biochemistry, microbiology, or related field Exp: 0 to 2 years |
You will be part of the High-Throughput Fermentation Process Engineering team and will work in a highly collaborative fashion to support efforts to develop high-throughput fermentation processes and use them to screen microbial strains for improved production of small molecules in automated mini-bioreactors. You will be part of an interdisciplinary department of fermentation/DSP scientists and engineers, automation engineers, software engineers, analytical chemists, and molecular biologists working to rapidly develop microbial strains to produce natural medicines. This person will report to the Lead Scientist for mini-bioreactor-based strain screening. | 12/03/2021 |
| 7694 | Demetrix Berkeley, CA Fermentation Process Engineer BSc or MSc (chemical engineering, microbiology, biological/life sciences or comparable degrees) Exp: 0-3 years |
Within Demetrix you will be part of the Upstream Process Engineering team within the department of Process Development. You will work closely with others to execute bench-scale fermentations to screen strains and develop improved fermentation processes. You will be part of an interdisciplinary team of fermentation/DSP scientists and engineers, automation engineers, software engineers, analytical chemists, and molecular biologists working to rapidly develop microbial strains to produce natural product medicines. | 12/03/2021 |
| 7695 | Demetrix Berkeley, CA Associate Scientist BS/MS in biology, chemical engineering, molecular biology, biochemistry, biophysics, cell physiology, or a related discipline Exp: 1-2 years |
DNA Operations is looking for an Associate Scientist to join our team! The DNA Operations team is responsible for high throughput molecular cloning and sequencing, and you will be part of an interdisciplinary team of scientists and engineers at Demetrix working to rapidly develop microbial strains to produce natural product medicines. | 12/03/2021 |
| 7696 | DICE Molecules South San Francisco, CA Research Associate / Senior Research Associate, In Vitro Pharmacology M.S. degree in biochemistry, biology, or a related field Exp: 0-2 years |
The successful candidate will be responsible for planning and independently performing experiments using a wide range of in vitro assays and technologies. These will include ELISA and mammalian cell culture assays, and will expand over time. This person will support cutting-edge small molecule discovery through their data and analysis within a growing multidisciplinary team. | 12/03/2021 |
| 7697 | DiscGenics Salt Lake City, UT Associate Analytical Scientist Bachelor’s in Biological, Biochemical or Chemistry related Exp: 1+ year |
The Associate Analytical Scientist will be responsible to support the analytical team in developing, qualifying and performing a variety of cellular and chemical test methods. This role interacts with all levels of the organization in a collaborative and positive way with colleagues to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. | 12/03/2021 |
| 7698 | Distributed Bio [Charles River] Mattawan, MI Research Associate - Bioanalytical MS/BS/BA in relevant field Exp: 0-2 years |
We are seeking a Research Associate for our Bioanalytical Department located in Mattawan, MI. The Research Associate is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others. | 12/03/2021 |
| 7699 | Distributed Bio [Charles River] Northridge, CA Research Associate I Bachelor’s degree in Biological Sciences required. Exp: 1 year |
This position is responsible for the evaluation of human blood products for manual or automated cell isolations, product manufacturer, and cell culture. Perform QC testing and create a certificate of analysis (COA) for products manufactured. Record isolation details on a processing worksheet using good documentation practices. Operate flow cytometer and basic lab equipment. | 12/03/2021 |
| 7700 | Distributed Bio [Charles River] Carlsbad, CA Research Associate Bachelor’s degree in Life Sciences or related discipline Exp: no experience |
We are seeking a Research Associate for our Insourcing Solutions site located in Carlsbad. The following are responsibilities related to the Research Associate: Performs technical tasks in the conduct of in vivo research studies or support services in accordance with good animal welfare practices. Prepares, collects and records research data and specimens in compliance with applicable regulations and SOPs. | 12/03/2021 |
| 7701 | Distributed Bio [Charles River] Cleveland, OH Research Associate 2 Bachelor’s degree in biology, chemistry, or related scientific related discipline. Exp: 1-2 years |
The Research Associate performs analytical method development, stability analysis and quantitative dose solution analysis in support of non-clinical safety testing studies and in accordance with general project plans, company standard operating procedures, applicable GLP regulations, timelines and company productivity standards. Responsibilities include but are not limited to: analytical method validation, conduct of the analysis according to validated methods, documentation of deviations and amendments, data review/approval, investigation of out-of-specification results, accurate incorporation of results and conclusions into study reports prior to review by the study director. The research associate also is responsible for analytical SOPs and analytical instrument GLP qualification. | 12/03/2021 |
| 7702 | Distributed Bio [Charles River] Mattawan, MI Research Associate - Formulations * $1000 Sign on Bonus 1 Bachelor’s/Master’s degree in a relevant field Exp: no experience |
A Research Associate - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. This position will be a Monday-Friday 6am -2:30pm schedule. | 12/03/2021 |
| 7703 | Distributed Bio [Charles River] S. San Francisco, CA Research Associate, Bioanalytical 1 Bachelor's degree (B.S./B.A.) or equivalent in a scientifically related discipline. Exp: 6 months |
We are seeking Research Associate candidates that are early in their careers and are highly motivated, enthusiastic and possess a passion for learning. This position will be involved in all aspects of studies supporting the bioanalysis of drug molecules in multiple matrices. This position is ideally suited to recent graduates who enjoy a fast-paced and collegial environment. The individual in this position will be responsible for working hands-on and under the direction of more senior staff in a dynamic environment where teamwork, data quality, innovation and speed are valued. | 12/03/2021 |
| 7704 | Diversigen St. Paul, MN Research Associate Masters degree in biology (or a related degree) Exp: 1 year |
The Research Associate supports microbiome-related R&D activities including designing and executing experiments both independently and under the direction of Diversigen scientists. The Research Associate is essential to our organization, supporting our work in the laboratory to help execute projects and services to design new products and/or technologies. This role requires strong experimental skills, diligent documentation, strong communication skills, and a collaborative attitude. Hands-on experience with next-generation short-read sequencing technologies is a must for this position. | 12/03/2021 |
| 7705 | Diversigen [OraSure Technologies] Bethlehem, PA Process Improvement Engineer I B.S. degree in Engineering (ChemE (preferred), ME, or MfgE) Exp: 1-2 years |
Support projects to improve the quality and efficiency of existing manufacturing processes as well as the scale-up, validation, and transfer of new products into manufacturing. | 12/03/2021 |
| 7706 | EAG Laboratories El Segundo, CA QC Microbiology Scientist Bachelor’s degree in Microbiology preferred Exp: 0 to 2 years |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a sample management specialist to work in our Professional Scientific Services QC group support the commercial release of life changing medicines in El Segundo, California. | 12/03/2021 |
| 7707 | EAG Laboratories San Diego, CA Quality Assurance Analyst: BioPharma Bachelor’s or Master’s degree in Chemistry or closely related science field Exp: one year |
Under general supervision, performs work that is varied and may be somewhat difficult in character. Audits and monitors various aspects of Eurofins Advantar Laboratories, Inc. for compliance with Good Manufacturing Practices (GMP) or in support of Good Laboratory Practices (GLP) by performing essential audits and training. This position will require working and interacting with different employees of the company. In addition, a detailed oriented and team player person is essential for this position due to high volume of work. Knowledge of electronic documentation systems is a plus as this person may be involved in the deployment of new Part 11 electronic systems and other supporting systems. Must have the ability to apply acquired knowledge of Good Documentation Practice (GDP) and GMP to daily tasks. Knowledge of cGMP, GLP, Eudralex Volume 4, and ISO regulations are a plus. | 12/03/2021 |
| 7708 | EAG Laboratories San Diego, CA Cell Culture Associate B.S. in Biology, Cell Biology, Molecular Biology, or related science Exp: 1 - 3 years |
Eurofins is searching for a Cell Culture Associate to provide assistance in a cell culture laboratory to support protein expression and cell line generation. | 12/03/2021 |
| 7709 | EAG Laboratories San Diego, CA Protein Purification Associate Bachelor's degree Exp: 1-3 years |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a Protein Purification Associate to support our Professional Scientific Services group in San Diego, CA. | 12/03/2021 |
| 7710 | EAG Laboratories San Diego, CA Molecular Biology Associate B.S. in Biological sciences (Molecular Biology, Biotechnology, Immunology, Biochemistry, or similar field) Exp: 1-3 years |
Eurofins Lancaster Laboratories PSS is searching for a Molecular Biology Associate to work in San Diego, CA. | 12/03/2021 |
| 7711 | Exponential Business and Technologies Eden Prairie, MN Nano Analytical and Testing Lab Technician BE or BS degree in Materials Science and Engineering, Mechanical Engineering, Physics, Chemistry or related disciplines Exp: One to two years |
Ebatco is seeking an energetic, self-disciplined, customer service oriented technical person to join its Nano Analytical and Testing Laboratory (NAT Lab). As a technical member of the NAT Lab team, the technician performs contract lab services and instrument demonstrations with appropriate levels of support and supervision, operates advanced nano/micro scale scientific instruments, collects testing and measurement data, and writes technical report on experimental results and observations. | 12/03/2021 |
| 7712 | Editas Medicine Waltham, MA Cell Manufacturing Associate I - 2180 BS in Biology-related field of study Exp: 1 - 2 years |
Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases. We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before. Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you. | 12/03/2021 |
| 7713 | Editas Medicine Cambridge, MA RA/SRA, iPSC Engineering - 2205 BS/MS in cell biology, molecular biology or related field Exp: 1-3+ years |
Editas Medicine is seeking a highly motivated Research Associate I/II to join our iPSC Engineering team and advance Editas’ cell-based medicines portfolio. In this role, you will join a team generating genetically engineered induced pluripotent stem cell (iPSC) lines and develop a clinically compatible, cutting-edge platform to edit, isolate and characterize clonal cell banks. | 12/03/2021 |
| 7714 | Elektrofi Boston, MA Research Associate/Intern BS (Associate) or Junior/Senior (Intern) in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biology, Bioengineering, or a related field Exp: 1+ years |
Elektrofi is looking for a Research Associate to join a team responsible for the development of platform formulations for Elektrofi’s proprietary microparticle production process. The Research Associate will play a key role in supporting the development of its biologics formulation platform. This individual will join an earlystage, multidisciplinary team of scientists and contribute to a variety of formulations activities in a highly collaborative environment. | 12/03/2021 |
| 7715 | Element Biosciences San Diego, CA Associate Scientist/Research Associate, Biochemistry Assay B.S. or M.S. degree Exp: 0-2 years |
As an Associate Scientist or Research Associate, you will contribute to the Protein Engineering/Biochemistry team and will work closely at the direction of scientists to characterize biochemical properties of product reagents. With mentoring, the candidate will be able to develop and optimize methods/techniques for testing and evaluation of novel biochemistry schemes and generate reports of findings. | 12/03/2021 |
| 7716 | Element Biosciences San Diego, CA Research Associate/Associate Scientist Bachelor’s degree in biology, chemistry, biochemistry, molecular biology, bioengineering, chemical engineering, or equivalent field of study Exp: 1+ years |
We are looking for a creative, enthusiastic, and highly motivated synthetic chemist to join the chemistry & Chemistry Discovery group at a well-funded and long-term multi-venture backed Life Sciences start-up company. The chemist will be involved in the development of reagents for our new NGS technologies. Expect to be part of a highly energetic and collaborative team. The position is at research associate/associate scientist level and is located at San Diego, CA. | 12/03/2021 |
| 7717 | Element Biosciences Sunnyvale, CA Associate Scientist II Bachelor’s degree in biology, chemistry, biochemistry, molecular biology, bioengineering, chemical engineering, or equivalent field of study Exp: 1+ years |
We are looking for a creative, enthusiastic, and highly motivated synthetic chemist to join the chemistry discovery group at a well-funded and long-term multi-venture backed Life Sciences start-up company. The synthetic chemist will be involved in the development of reagents for our new NGS technologies. Expect to be part of a highly energetic and collaborative team. The position is at research associate/associate scientist level and is located at Sunnyvale in Bay Area. | 12/03/2021 |
| 7718 | Element Biosciences San Diego, CA Research Associate - Biochemistry, Enzymes & Reagents B.S. degree in biology, molecular or cell biology, biochemistry, biological physics, bioengineering, chemical engineering, or equivalent field of stud Exp: 0-2+ years |
The Reagent Development group is seeking a Research Associate to assist with ongoing preparation of product for market and R&D of new sequencing biochemistry. In this position, candidates will carry out assays to assist in better understanding our reagents to improve the data quality and customer experience. Candidates are expected to be familiar with common laboratory techniques and be eager to learn under the direction of scientists. With mentoring, candidates will be able to develop and optimize methods and techniques for the testing and evaluation of cutting-edge sequencing reagents. | 12/03/2021 |
| 7719 | Entrada Therapeutics Boston, MA Research Associate I/II, Neuromuscular and Cardiac Biology RA I - B.S./M.S. in Molecular/Cellular biology or a related field Exp: 0-2 years |
In this position, you will be part of a cross-functional team exploring new therapeutic programs for neuromuscular and cardiovascular disease areas. You will play a critical role in both in vivo and ex vivo aspects of pre-clinical POC studies including functional testing. | 12/03/2021 |
| 7720 | Enzo Life Sciences Farmingdale, NY Manufacturing Scientist I- Immunoassays MS in Molecular Biology, Genomics, Biochemistry or other similar areas Exp: 1+ years |
This position is responsible for the manufacturing and testing of immunoassay kits, chemicals, and reagents serving the life sciences, and ensuring product quality based on thorough science. Integral to the kit production process, the Manufacturing Scientist I will assist in all phases of kit product release, including the choice of critical raw materials, selection of release criteria, and the validation, testing, and optimizing of kit components. As part of the manufacturing team, this position will share matrixed responsibilities with team members to meet kit production goals. | 12/03/2021 |
| 7721 | BioAssay Systems Haywood, CA Research Associate - Assay Development A bachelors degree in biochemistry, chemistry, biology, or related field Exp: 1-2 years |
We currently have an exciting opportunity for an enthusiastic research associate to join our growing R&D team. This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers. | 11/12/2021 |
| 7722 | BioAssay Systems Haywood, CA Research Associate - Manufacturing A college degree in chemistry, biochemistry or biology Exp: 1-2 years |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing, and packaging the finished products. This candidate may also join part time in our R&D team. | 11/12/2021 |
| 7723 | BioFire Diagnostics Salt Lake City, UT Research Associate B.S. in chemistry, biology, or a related field Exp: 0-1 years |
The Template Control Research Associate (RA) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The RA-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. The RA-I will receive general instruction on routine work, perform lab duties with minimal supervision, and receive training and additional instruction for new tasks as needed. Substantial preference will be given to candidates who hold a B.S. in chemistry, biology, or a related field, | 11/12/2021 |
| 7724 | BioLegend San Diego, CA Research Associate- Diagnostics Bachelor’s degree in a Life Sciences-related field Exp: 1 years |
BioLegend is seeking a highly motivated Product Development Research Associate to join our Diagnostic Product Development Team. This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report. | 11/12/2021 |
| 7725 | BioLegend San Diego, CA Research Associate - Hybridoma and Cell Culture S. or M.S. in Biology, Immunology or another related field Exp: 1 year |
The Research Associate will be involved in product development and optimization of cell culture process and new product development. In particular, he/she will be involved in determining the feasibility of new products and new cell culture processes for in-house and custom projects. This role will also be involved in troubleshooting issues associated with cell culture. This role requires mammalian cell culture experience. Knowledge of process development for antibody production, particularly hybridoma, on a small and large scale is a plus. | 11/12/2021 |
| 7726 | BioLegend San Diego, CA Biochemist - BV Conjugation AM Shift (6:00am-2:30pm) Bachelor of Science in Biology/Chemistry or related area Exp: 1 years |
The Biochemist position for BioLegend’s Conjugation Group will be responsible for performing all essential functions related to antibody conjugation, including following SOPs and batch records and maintaining and analyzing lot histories. The Biochemist will be an integral member of a team that ensures the highest quality of our finalized antibody products. This position offers the opportunity to gain experience with different types of conjugation chemistries and different chromatography methods to purify antibodies and offers the opportunity to work in small scale to large scale product projects and to learn to utilize the (Enterprise Resource Planning) ERP database to track production schedules and deadlines and to enter production results. This position will also perform scale-ups and perform troubleshooting of problematic products, including continuous improvement methodologies for efficiency. | 11/12/2021 |
| 7727 | BioLegend San Diego, CA Biochemist- Purification PM Shift (2:30pm-11pm) Bachelor of Science in Biology/Chemistry or related area Exp: less than 1 year |
BioLegend has an opening for a self-motivated individual with production experience in a fast moving and dynamic environment to join our Purification team! The Biochemist will be an integral member of a team, that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform column chromatography, troubleshooting of problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 11/12/2021 |
| 7728 | BioLegend San Diego, CA Biochemist - Purification Bachelor of Science in Biology/Chemistry or related area Exp: less than 1 year |
The Biochemist I-III will be an integral member of a team, that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform column chromatography, troubleshooting of problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 11/12/2021 |
| 7729 | BioLegend San Diego, CA Biochemist- Process Development Group Bachelor’s degree in Biochemistry, Bio-Organic Chemistry, Chemistry, or Science Exp: 1 year |
The Process Development Associate will be an integral member of a team that manufactures and provides antibodies and reagents to a diverse set of research areas. The Process Development Associate will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position, you will perform troubleshooting, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross-train on a variety of other supporting tasks. | 11/12/2021 |
| 7730 | Bio-Rad Pleasanton, CA Research Associate I BS in Molecular Biology or Biochemistry Exp: 0-2 years |
We are looking for a Research Associate I to join our Product Development team at Bio-Rad – Digital Biology Group. | 11/12/2021 |
| 7731 | Bio-Rad Woodinville, WA Production Chemist I A Bachelors degree in a life science or related field. Exp: 0 - 3 years |
Manufacturing activities for BioPlex 2200 to support commercialization and development activities. Areas of responsibility could include bead coupling, conjugation, calibrator and control manufacturing, or other component manufacturing. | 11/12/2021 |
| 7732 | Bio-techne Minneapolis, MN Research Associate, Array Manufacturing bachelor’s degree in chemistry, biological sciences or equivalent Exp: 0 to 2 years |
This position is responsible for preparing intermediate antibody cocktails for various product lines, participating in Proteome Profiler Array printing, and performing in-process Array component testing. In addition, this position is responsible for BioRobotics MicroGrid II MicroArrayer start up and/or take-down, basic maintenance and troubleshooting. | 11/12/2021 |
| 7733 | Bio-techne Minneapolis, MN Research Associate, Protein Purification Bachelors or Masters degree in Biochemistry or equivalent degree Exp: Entry-level |
We are seeking a Research Associate for Bio-Techne's Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. | 11/12/2021 |
| 7734 | Bio-techne San Jose, CA Research Associate Bachelor's Degree in biotechnology, biochemistry, or related field Exp: up to 3 years |
The Applications Science team is seeking a highly motivated Research Associate to join their ranks! In this position, you will work daily with innovative analytical platforms alongside our scientists to contribute exciting data for scientific collateral and custom projects. As part of this team, the Research Associate is also expected to join support efforts to put out fires (escalations) via instrument testing, assay testing, etc. | 11/12/2021 |
| 7735 | Bio-techne Minneapolis, MN Research Associate for Immunoassay Reagent Equivalence and Qualification bachelor’s degree in Biology, Biochemistry or equivalent Exp: 0 to 2+ years |
This entry to mid-level position is a >75% bench-based position that will execute antibody, protein, and raw material equivalence testing across multiple immunoassay platforms. This will ensure Bio-techne continues to have superb lot-to-lot consistency and prevent supply disruptions to ensure customer satisfaction. Plan and perform appropriate experiments, and report final conclusions with guidance from senior associate(s) and/or supervisor. This position functions collaboratively with multiple departments. Projects will be diverse, with the focus being on multiple immunoassay platforms (Luminex, ELISA Quantikine, QuicKit, SimplePlex, DuoSet and Arrays). Equivalence processes will increase quality, reproducibility, reduce backorder times, further reduce failure rate & decrease redundant/unnecessary testing. | 11/12/2021 |
| 7736 | Bio-techne San Marcos, CA Chemist - Manufacturing Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 years |
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 11/12/2021 |
| 7737 | Bio-techne Minneapolis, MN Research Associate Antibody Production Bachelor’s degree in chemistry, biology, biochemistry or equivalent Exp: 0 to 2 years |
As an Antibody Purification Research Associate you will be responsible for performing antibody purifications and conducting in process testing of product. | 11/12/2021 |
| 7738 | BioVision Milpitas, CA Biotech Production Associate B.S. degree in biology or chemistry related fields Exp: 1-2 years |
We are looking for a highly motivated individual to work in our production department as a Production Associate. | 11/12/2021 |
| 7739 | Jubilant Cadista Spokane, WA Microbiologist I (Monday-Friday) Bachelor of Science Degree with emphasis in Microbiology or Biology with Micro emphasis –or closely related hard science required. Exp: No experience |
The Microbiologist I will perform the microbiological analysis on Allergenic and Contract Customer raw materials, intermediates, and finished products following prescribed procedures to provide data required to determine raw material/product disposition. Obtain full familiarity of the activities associated in the Microbiology Laboratory. This does not include proficiency of the actual test methods, but a comprehensive understanding of the activities associated to the Microbiology Lab. | 11/12/2021 |
| 7740 | Calico South San Francisco, CA Research Associate, Oncology BS or MS degree in Biology, Molecular Biology, Biochemistry, Chemistry or related discipline. Exp: 0-5 years |
The successful candidate will work closely with their Calico and partner colleagues to support work on further understand the biology of promising therapeutic targets in oncology. The candidate will also enable and participate in drug discovery programs for those targets. | 11/13/2021 |
| 7741 | Casma Therapeutics Cambridge, MA Research Associate, Biology Bachelor’s degree in biology or related discipline Exp: 1 year |
We are seeking a highly motivated, Senior Research Associate/Associate Scientist Associate to participate in drug discovery programs that lead to the identification of new targets and drug candidates for clinical development. The individual should possess strong core competencies in cell biology, molecular biology, assay development. We are seeking a qualified candidate who will share our excitement about the science, contribute to our culture, and honor our commitment to patients. | 11/13/2021 |
| 7742 | Catalent Madison, WI Assistant Scientist, Cell Line Development - SIGN ON BONUS OFFERED MS in Biotechnology, or related field; Bachelors or Associates Degree in Biotechnology, or related field Exp: MS- 0 years; AS/BS- 1 to 3 years’ |
The Cell Line Development team is responsible for using the patented GPEx® technology to create high performance stable cell lines using a non-replicative retrovector system. This system can be used with any mammalian cell line and many eukaryotic cell lines. This position will perform a variety of laboratory procedures to support Cell Line Development. These procedures include creation of stable continuous cell lines, routine maintenance of cell lines, accurate documentation, participation in experiments, following client timelines. | 11/13/2021 |
| 7743 | Catalent Morrisville, NC Associate Scientist Bachelor’s Degree in Chemistry or closely related physical science Exp: 1+ years |
Catalent is looking to hire an Associate Scientist to join a dynamic team at our Morrisville, NC site. The Research Triangle Park (RTP) facility is Catalent's Center of Excellence for Analytical Services and is also home to Catalent's Inhalation franchise including product development, clinical and commercial manufacturing for pMDI, DPI, and Nasal Sprays. | 11/13/2021 |
| 7744 | Catalent Kansas City, MO Associate Scientist Bachelor's degree in chemistry or closely related physical science. Exp: 1-3 years |
The Associate Scientist will work under general supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility. Some evaluation, originality or ingenuity is required. Follows established protocols and work plans. The Associate Scientist may be assisted by laboratory technicians / assistants. Comply with divisional and site Environmental Health and Safety requirements. | 11/13/2021 |
| 7745 | Catalent Bloomington, IN Associate Quality Control Scientist - Monday - Friday; 3PM - 11:30PM Bachelor’s degree/Master's degree in science field Exp: BS: 0-3 years; MS: 0-2 years |
As an Associate QC Scientist, your primary duty will be to provide quality control environmental monitoring, critical utility systems, in-process, finished products, stability, cleaning process, and analytical method validation testing according to SOPs, cGMPs and regulatory guidelines. This is a full time position; Monday - Friday; 3:00PM - 11:30PM | 11/13/2021 |
| 7746 | Catalent Winchester, KY Microbiologist - Second Shift Bachelors Degree in Microbiology, Biology or Chemistry (Preferred in Microbiology or Biology) required Exp: 0+ years |
The Microbiologist is primarily responsible for performing complex, non-routine microbiological analyses, and therefore must be capable of recognizing the need for pathogen identification, solving microbiological system problems, and leading and completing microbial investigations related to the water system, environmental monitoring of production equipment and the air handling system. The work is hands on and maintains the microbial testing needed to support raw materials, finished goods and environmental monitoring for the facility. Work hours: 2nd shift Monday – Friday 3 pm – 11:30 pm (Work week starts Monday) | 11/13/2021 |
| 7747 | Catalent San Diego, CA Analytical Chemist I BS degree in a physical, chemical, biological, or pharmaceutical science required Exp: 0+ years |
Catalent Pharma Solutions is looking to hire an Analytical Chemist I for our San Diego, CA team. This a great entry-level opportunity for a new grad looking to gain hands-on industry experience and learn a variety of lab techniques. The Analytical Chemist I will be expected to understand and execute basic analytical procedures in order to assess the quality of pharmaceutical API, intermediates, and final drug products under limited supervision. Duties may include the preparation of simple aqueous and organic buffered solutions, volumetric dilution of samples and standards using good laboratory techniques, clear and accurate record keeping in laboratory notebooks, use of analytical instrumentation to acquire raw data, calculation and reporting of final results. The Chemist I will begin to develop product-specific cleaning methods to support use of GMP manufacturing equipment. All duties will be performed in compliance with company standard operating procedures (SOPs) and GMP regulations, as appropriate. The shift is Monday-Friday 7:30am-4pm. | 11/13/2021 |
| 7748 | Cellares South San Francisco, CA Research Associate, Process Development BS/MS or equivalent in Bioengineering, Chemical Engineering, Biology, Biochemistry, or related field Exp: 1-2 years |
Cellares is seeking an innovative and highly motivated Research Associate to join the Process Development team. This individual will interface across many parts of the company and contribute significantly to the development of our advanced cell therapy manufacturing platform. | 11/13/2021 |
| 7749 | Celldex Therapeutics Fall River, MA Associate Scientist B.S. in Biochemistry, Bioengineering or related field is required. Exp: 1-3 years |
As an Associate Scientist you will have the unique opportunity to work with a team to develop purification processes for recombinant antibodies and recombinant proteins This role will be full time at our Fall River facility and reports into the Senior Manager, Process Development Engineering. | 11/13/2021 |
| 7750 | Celldex Therapeutics Fall River, MA Associate Scientist/Scientist I BS or BA in Biology or a related field. Exp: 1-3 years |
As an Associate Scientist/Scientist, you will have the unique opportunity to work in a variety of functions related to assay development/validation, GLP sample analysis, cell culture, in vivo tumor studies, flow cytometry, and laboratory maintenance. You will join a team performing preclinical research and bioanalytical testing in support of nonclinical toxicology studies and human clinical trials assessing the safety and efficacy of Celldex’s pipeline, including novel immuno-inflammatory and immuno-oncology therapies. | 11/13/2021 |
| 7751 | Cellectis New York, NY Research Associate I/II, Gene Editing Platform BS/MS in molecular biology, biochemistry or related discipline. Exp: 1-4 years |
We are seeking a highly creative and motivated individual to join us in developing the next generation of gene editing technologies. The successful applicant will have a strong scientific background and proven accomplishments in next generation sequencing technologies (library prep, quality control, sequencing hardware), in molecular/cellular biology and a passion for genome editing and gene therapy. As part of the gene editing platform, the candidate will contribute to our ongoing efforts toward the development of differentiated therapeutic approaches using our gene editing technologies. Candidates should be highly self-motivated with the ability to excel in a fast-moving, goal-oriented environment. | 11/13/2021 |
| 7752 | Cellectis Raleigh, NC QC Analyst, Microbiology/Environmental Monitoring (EM) Bachelor's degree Exp: 1-5 years |
The QC Analyst, Microbiology/Environmental Monitoring will be responsible for supporting and ensuring GMP manufacturing operations at Cellectis’ GMP manufacturing facility in Raleigh NC.. The incumbent will support the development, qualification and requalification of the isolator decontamination cycles. The Microbiology/ EM analyst will also perform daily Microbiology laboratory activities and documentation including, but not limited to rapid sterility (BacT/Alert) testing, kinetic endotoxin testing and environmental monitoringThe QC Analyst will support investigations for OOS and other non-conforming results. The analyst will also author and review procedures, protocols, and reports. | 11/13/2021 |
| 7753 | Century Therapeutics Greater Philadelphia, PA Research Associate/Senior Research Associate, MSAT BS or MS degree in biochemical, chemical, biomedical engineering or other related field Exp: RA:0-2 years |
The Senior Research Associate/Research Associate, Process Engineering will be responsible for implementing, developing and executing manufacturing processes for Century’s cellular therapy programs. This role will be expected to be trained in Philadelphia for up to 6 months before being permanently located at the site in Branchburg, NJ. The candidate will be expected to receive process tech transfers, implement them into a GMP manufacturing facility, and be a hands on operator for the Phase I manufacturing campaign. This role is also responsible for ongoing process development on these programs including scale up and characterization. This role requires extensive collaboration with internal and external teams. The successful candidate will need strong scientific background, interpersonal skills, and ability to work collaboratively with other groups across organizations. This role is based in Philadelphia (University City), PA for approximately 6 months and then permanently in Branchburg, NJ. | 11/13/2021 |
| 7754 | Champions Oncology Rockville, MD Research Technician II/III , Cell Culture (in vivo) MS (RT II) Exp: 1 years |
Support Ex-vivo / In-vivo oncology studies as a member of the in vivo Cell Culture Team. Duties and responsibilities are: Responsible for inventory and culturing of human and mouse cancer cell lines for cell line xenograft studies Perform basic and advanced cell culture, including culturing primary cells and characterizing their growth Produce, maintain, and characterize cultured cells, as directed Conduct Leukopak PBMC sample processing | 11/13/2021 |
| 7755 | Chromatan Springhouse, PA ASSOCIATE SCIENTIST I Bachelor of Science degree in Chemistry, Biochemistry, Chemical Engineering or a related field Exp: 0-2 years |
This position will support the downstream purification team for development and implementation of a fully integrated end to end continuous bio-production platform fully enabled with PAT. This position will focus on evaluating continuous operation technologies using quality by design techniques, to develop and optimize novel, continuous recovery and purification processes, for recombinant proteins and biological macromolecules. The applicant should have experience in laboratory research, and a desire to continue in a laboratory-focused role. The position will interface with a small team of scientist and engineers focused on continuous chromatography process development and technology transfer to demonstration scale production. | 11/13/2021 |
| 7756 | Alkermes Waltham, MA Contract, Research Associate, Biology BS/MS in cell biology, oncology, immunology, or related subject Exp: BS: 1-3 years; MS: 0 years |
Alkermes has an excellent opportunity for a highly talented biologist with a strong background in cell / molecular biology. The research associate level position is currently a contract research scientist for 12 months with possibility of renewal. | 10/26/2021 |
| 7757 | Alkermes Waltham, MA Contractor, Analytical Development - Biologics MS degree in a scientific field (Biology, Biochemistry, Chemistry, etc.) Exp: 1+ years |
The Contractor position resides within the Analytical Research Group which is a part of Analytical Development (AD) organization. The successful candidate will utilize advanced analytical to characterize a variety of biotherapeutics from discovery, through clinical development, to commercialization. He/she will thrive in a highly collaborative matrix team environment to enable critical decision-making and ensure the successful development of new drugs. | 10/26/2021 |
| 7758 | Alkermes Waltham, MA Contractor, Analytical Development - Small Molecule MS degree in a scientific field (Biology, Biochemistry, Chemistry, etc.) Exp: 1 year |
The Contractor position resides within the Analytical Research Group which is a part of Analytical Development (AD) organization. The successful candidate will utilize advanced analytical to characterize a variety of molecules from discovery, through clinical development, to commercialization. He/she will thrive in a highly collaborative matrix team environment to enable critical decision-making and ensure the successful development of new drugs. | 10/26/2021 |
| 7759 | Alkermes Waltham, MA Senior Research Associate/Scientist Senior Research Associate: MS Exp: 1-5 years |
Alkermes is searching for a highly talented Sr RA/Scientist responsible for developing and evaluating cutting-edge technologies and concepts for protein engineering. The newly designed proteins are expected to be the first- or best-in-class biologics to support early drug discovery in multiple disease areas, including oncology, immunology, fibrosis and others. | 10/26/2021 |
| 7760 | Alkermes Waltham, MA Senior Research Associate II M.S. in chemistry, biochemistry, pharmaceutics or related biological/physical science. Exp: 1-5+ years |
This position is primarily responsible for pre-formulation assessment and formulation support for discovery stage and early development small molecule candidates and formulation support for large molecule candidates. This individual will participate in project teams and provide deliverables within project timelines. The successful candidate will contribute to the scientific and technical community at Alkermes by effectively supporting programs in a laboratory-based role and providing informed opinions based on interpretation of results and project deliverables. | 10/26/2021 |
| 7761 | Allogene Therapeutics South San Francisco, CA Associate Scientist, Flow Cytometry Bachelor’s degree or master’s degree in immunology, cell biology or related field Exp: 1-5 years |
Allogene is seeking a highly determined, results-oriented, self-starter who demonstrates personal accountability for outcomes and is motivated by increasing levels of responsibility, to join a dynamic team responsible for successful development and characterization of clinical-scale manufacturing of Allogeneic Chimeric Antigen Receptor T-cell therapies (Allo CAR T™). The successful candidate will help to support appropriate flow cytometry-based analytical methods for the characterization, release and stability testing of CAR T products. | 10/27/2021 |
| 7762 | Allogene Therapeutics South San Francisco, CA Assoc. Scientist/Sr Assoc. Sci, Process & Product Development MS or BS in Biochemistry, Molecular & Cell Biology, Immunology or the related field Exp: 1-3 years |
Allogene is seeking an Associate Scientist/Senior Associate Scientist to support the development and characterization of clinical-scale manufacturing processes for Allogene’s CART therapies. This individual will contribute to the development, implementation and characterization of state-of-the-art processing technologies to deliver scalable and robust manufacturing processes, and support successful tech transfer for GMP manufacturing and release at a CMO. This position will also contribute to the development of novel technologies and approaches to meet future CART manufacturing needs. | 10/27/2021 |
| 7763 | Allogene Therapeutics South San Francisco, CA Scientist/Senior Associate Scientist, Analytical Development Masters Exp: 0-6 years |
We are seeking a highly motivated Associate Scientist/Scientist to join Allogene’s Process and Product Development Group to support the Analytical Development activities. (S)he will play a key role in CART cell therapy related analytical assay development. (S)he will work closely with internal and external partners to ensure the assay development, execution of the release and characterization assay, assay qualification, comprehensive risk assessments, data synthesis that allows for the subsequent analytical assay tech transfer. | 10/27/2021 |
| 7764 | Allogene Therapeutics Newark, CA Analyst I, QC Microbiology (Contract) Bachelor’s degree in Microbiology preferred Exp: 1 year |
Allogene is seeking a highly motivated individual to join us as an Analyst I, QC Microbiology. This position provides Quality Control microbiological testing for clinical and commercial manufactured product, responsible for product testing, utility testing and environmental monitoring. This is a 6+ month contract opportunity in Newark, CA. | 10/27/2021 |
| 7765 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II BS or MS in Chemistry, Biochemistry or related disciplines. Exp: 1-3 years |
The Associate Scientist II, Specifications will be responsible for providing support for siRNA isolated intermediates, drug substances, drug products, and critical raw materials, with regards to setting specifications. | 10/27/2021 |
| 7766 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, In VItro BS in a biological science Exp: 1 year |
We are currently seeking a passionate and experienced Research Associate Scientist II with background in in vitro screening to join our dynamic, fast-paced and interdisciplinary lead development team. Our mission is to advance novel RNAi therapeutic programs from target discovery through lead candidate selection. The successful candidate will be technically skilled in biochemistry or cell biology, and bring a rigorous, analytical approach to research. | 10/27/2021 |
| 7767 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 10/27/2021 |
| 7768 | ALVEO Technologies Alameda, CA Assay Development and Verification Scientist I BA/BS degree in Biochemistry, Molecular Biology, Microbiology or related field Exp: 1-3 years |
Alveo Technologies is looking for a Development and Verification Scientist I to support ongoing V&V efforts of projects in disease detection. The successful candidate will assist in planning and executing protocols / conducting experiments at the bench to meet objectives. The candidate should be able to review, understand and follow the instructions, protocols and SOPs provided by the R&D and Manufacturing departments. | 10/27/2021 |
| 7769 | Norwich Pharmaceuticals Pine Brook, NJ Research Associate MS in Chemistry, Biochemistry, Microbiology or Biology or related discipline. Exp: 1-3 years |
Working somewhat independently, provides analytical support of new formulation development samples of Solid Oral Dosage forms. The primary focus will be to support the physical (particle size, viscosity, etc.) and chemical (dissolution, assay, content uniformity, related compounds etc.) characterization of internally developed SOD formulations and Reference Listed Drug products. and formulation testing, accurately and concisely documents data, and reports results. | 10/27/2021 |
| 7770 | Ambry Genetics Aliso Viejo, CA Research Associate I BS or MS degree in a life sciences field: Biology, Molecular Biology, Biochemistry or related field. Exp: 0-2 years |
Research Associate I is responsible for assisting senior R&D staffs to design, develop, and validate clinical diagnostic assays spanning a wide range of Next-Generation sequencing and microarray technologies. | 10/28/2021 |
| 7771 | Ambry Genetics Aliso Viejo, CA Research Associate II MS degree in a life sciences field: Biology, Molecular Biology, Biochemistry or related field. Exp: 1-2 years |
Research Associate II is responsible for assisting senior R&D staffs with minimal supervision to design, develop, and validate clinical diagnostic assays spanning a wide range of Next-Generation sequencing and microarray technologies. | 10/28/2021 |
| 7772 | Amunix Pharmaceuticals South San Francisco, CA Research Associate I/II (Temporary Hire) Bachelor's degree in a scientific discipline Exp: 1+ years |
We are seeking a detail oriented and highly motivated Research Associate to join the assay development team in Bioanalytical Sciences at Amunix Pharmaceuticals. This is a full-time, temporary position. | 10/28/2021 |
| 7773 | Amunix Pharmaceuticals South San Francisco, CA Research Associate I/II, Assay Development Bachelor's degree in a scientific discipline Exp: 1+ years |
We are seeking a detail oriented and highly motivated Research Associate to join the assay development team in Bioanalytical Sciences at Amunix Pharmaceuticals. | 10/28/2021 |
| 7774 | AnaptysBio San Diego, CA Research Associate I BA/BS in biology-related discipline or MS in biology-related discipline Exp: BS: 0-5 years; MS: 0-2 years |
The Research Associate I in Discovery Biology will perform laboratory research for AnaptysBio projects, in collaboration with others. The individual will utilize well established protocols to assay human immune cells or cell lines in basic immunology experiments. This position will development their expertise in the use of appropriate laboratory equipment, good laboratory procedures and practices, presenting data clearly and effectively at internal meetings, and documenting experimental data in an electronic laboratory notebook in accordance with company policy. | 10/28/2021 |
| 7775 | AnaSpec Fremont, CA Research Associate - Biology B.S in Biochemistry, Chemistry, or related discipline. Exp: 0-3 years |
Perform assay kit production and QC tests: enzyme activity assays, protein expression, purification. Manage orders, maintain inventory. Perform protein labelling and conjugation procedures. Prepare product datasheets, SOPs. | 10/29/2021 |
| 7776 | ANI Pharmaceuticals Baudette, MN Analytical Development Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field or major. Exp: 1-3 years |
Perform review of data collected under approved test methods and investigational plans and protocols, in accordance with governing SOPs. Provide accurate assessment of data integrity, and document findings. Work with management and peers to correct deficiencies. | 10/29/2021 |
| 7777 | Antibody Solutions Santa Clara, CA Research Associate Cell Biology A Bachelor's degree in a biology-related field, such as Cell Biology, Molecular Biology, Microbiology, Biochemistry, etc. Exp: 0-2 years |
We are seeking an entry level Research Associate for our Cell Biology department. The successful candidate will work with a team dedicated to the cellular aspects of antibody discovery. Responsibilities include isolation and immortalization of B-cells, cloning by FACS-sorting, cryopreservation & cell banking, and antibody production using bioreactors. Antibody Solutions is a leading Contract Research Organization (CRO) in antibody-related services. | 10/29/2021 |
| 7778 | Antibody Solutions Santa Clara, CA Research Associate Immunochemistry A Bachelor's degree in a biology-related field, such as Cell Biology, Molecular Biology, Microbiology, Biochemistry, etc. (Required). Exp: 0-2 years |
We are seeking an entry level Research Associate for our Immunochemistry department. The successful candidate will work with a team dedicated to the analysis of polyclonal sera and monoclonal antibodies for antibody discovery. Responsibilities include antigen and buffer formulation, designing and performing ELISA, Flow Cytometry, Biolayer Interferometry, and ELISpot assays, and data compilation and analysis. | 10/29/2021 |
| 7779 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. | 10/29/2021 |
| 7780 | Atalanta Therapeutics Boston, MA Associate Scientist II / Senior Associate Scientist – siRNA Screening Master’s degree in biochemistry or relevant biological science Exp: 0-5 plus years |
Atalanta Therapeutics is seeking an experienced and highly motivated Associate Scientist II / Senior Associate Scientist to be part of the dynamic and collaborative In Vitro Biology team. This individual will contribute to cell-based screening of therapeutic oligonucleotides under direction of the HTS lab head. S/he will be responsible for routine cell line maintenance, optimization of medium to high-throughput cellular assays to quantitate mRNA or protein marker levels, and execution of siRNA efficacy screens to support preclinical drug development for multiple therapeutic targets. | 10/29/2021 |
| 7781 | Atalanta Therapeutics Boston, MA (Senior) Associate Scientist/Scientist I, In Vivo Pharmacology (Molecular Biology) Master’s Degree Exp: 0-3 plus years |
Atalanta is seeking a highly skilled and motivated (Senior) Associate Scientist/Scientist to join the in vivo pharmacology group to support Atalanta’s drug discovery programs. This individual will have a strong background in molecular and biochemical assays and method development with hands-on experience in processing CNS tissue and molecular analysis to assess target gene and protein expression. We are seeking candidates who thrive in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. | 10/29/2021 |
| 7782 | Atara Biotherapeutics Thousand Oaks, CA Research Associate/Sr. Research Associate - Analytical Development Bachelor’s Degree or Master's Degree Exp: RA-BS: 1-year ; Sr.RA-MS |
This position works with the Technical Operations teams to develop and/or improve cell assays for cell product characterization and release. The Research Associate or Senior Research Associate participates in laboratory activities to support process development, evaluate and develop new assay methods, and perform product characterization for Atara’s allogeneic cytotoxic T cell products. | 10/29/2021 |
| 7783 | Atara Biotherapeutics Thousand Oaks, CA Research Associate/Sr Research Associate, Pre-Clinical Bachelor’s degree Exp: 1+ years |
The Research Associate/Senior Research Associate, CAR-T Development is an integral member of the Preclinical Immunotherapy Research group. The Senior Research Associate, CAR-T Development will serve as a technical expert in the generation and characterization of novel CTL and Chimeric Antigen Receptor (CAR) T cell therapies. | 10/29/2021 |
| 7784 | ATUM Newark, CA Protein Purification Associate (Mammalian) Bachelor’s degree in Biology or related field Exp: 1 - 3 year’s |
This an entry-level position within our mammalian protein purification group. The ideal candidate will be responsible for purification and characterization of a variety of protein types including therapeutic proteins, antigens and assay reagents expressed in mammalian cells. They will not be satisfied with just doing their part, but will thrive on being part of a collaborative team that aims to continually improve. Proteins will be purified at various scales ranging from high throughput robotic purification to many grams. Additionally, the incumbent will have opportunities to learn cell culture, bacterial and yeast fermentation in addition to bioanalytical techniques. | 10/29/2021 |
| 7785 | ATUM Newark, CA Cell Culture Lab Associate BS/MS in Biology, Molecular Biology, Cell Biology, Biochemistry or related field Exp: 1-2 years |
ATUM is in need of an entry level Production Associate for our Cell Line Development team. The ideal candidate will have a Bachelor's degree in Biology or a related field, 1-2 years of industry experience working with HEK and CHO cell lines, and cell culture techniques. | 10/29/2021 |
| 7786 | August Bioservices Nashville, TN Microbiologist I B.A./ B.S in Biology (or related) Exp: 0–2 years |
Reporting to the Manager, Microbiology, the Microbiologist I will be responsible for performing biological assays of raw materials, in-process samples, finished product, and environmental monitoring samples. He/she will work with microbiology personnel to assure test results, procedures, and methods are written, maintained, executed, and approved in accordance with approved SOPs and regulatory requirements. | 10/29/2021 |
| 7787 | Avantor Sciences Phillipsburg, NJ Chemical Technician Bachelor’s degree Exp: one + year |
The entry level Chemical Technician (Bachelor's Degree Required) is responsible for completing procedures associated with manufacture of pilot scale chemical batches. | 10/29/2021 |
| 7788 | Aziyo Biologics Silver Spring, MD R & D Associate Master’s degree in Biological Sciences, Engineering, or a related Life Sciences field. Exp: 1-3 years |
This position will work in a collaborative team environment to design assays for the scientific characterization and development of tissue-based and biomaterial products in compliance with Aziyo’s quality and regulatory standards. The ideal candidate is able to effectively handle multiple tasks, while learning and adapting to different projects. The successful candidate will execute, optimize, and analyze a broad range of bioassays, biomechanical and material characterizations, and product prototyping. In addition, this position will support the development of manufacturing processes, including scale up for full production and/or production transfer. The position will also supply scientific data for use by Aziyo’s marketing department. Position reports to the Principal Scientist in Silver Spring | 10/29/2021 |
| 7789 | Baxter Cleveland, MS Quality Lab Assoc II B.S. Degree in Science (Chemistry, Chemical Engineering, Physical Chemistry, Biology) Exp: 0-3 Years |
Perform chemical and physical analysis on medical products through all stages of the manufacturing process from incoming raw materials through to product release. Areas include raw materials, initial, in-process and finished products, Stability Program, protocol support, instrumental analysis and instrument calibration/qualifications. Responsibilities also include adherence to regulatory and procedural requirements that govern the operations and products (e.g., Specifications and Cleveland standard operating procedures). | 10/29/2021 |
| 7790 | Baxter Round Lake, IL Quality Lab Associate 2nd Shift Bachelors Degree in microbiology or Biological Science Exp: 0-2 years |
Conduct critical biological, chemical, and physical analysis on raw materials; initial, in-process and final products; and samples collected from environmental monitoring programs at the Round Lake Drug Delivery facility. | 10/29/2021 |
| 7791 | Baxter Marion, NC Validation Analytics Associate III Master’s/ Ph.D. degree in Natural Sciences Exp: 1-3 years’ |
Responsible for performance and efficiency of Analytical Validation and Qualification activities. Lead and/or coordinate activities in support of analytical validation operations to ensure: safe operations, effective planning, and regulatory compliance in the performance of method, process, cleaning, and stability validations for various chemical products while maintaining high standards for quality and responsiveness to production requirements. | 10/30/2021 |
| 7792 | Baxter Mountain Home, AR Quality Lab Associate I- Chemistry Bachelor of science in Chemistry or any science related field (Chemistry Preferred) Exp: 0-2 years' |
Responsible for the outgoing quality, safety, and efficacy of product produced at Mountain Home (relative to Chemistry Laboratory analyses) involving complex routine and non-routine testing and validation in the Chem Lab. | 10/30/2021 |
| 7793 | Baxter Round Lake, IL Quality Lab Associate 3rd Shift Bachelors degree in Chemistry or Science related degree Exp: 6 months + |
The Quality Lab Associate I will be located at the Drug Delivery Chemistry Laboratories, Round Lake, IL. The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. This is a third shift position but will be required to work on weekends to support training of analysts and to support projects and/or production, as required. | 10/30/2021 |
| 7794 | Becton Dickinson San Diego, CA Research Associate II Bachelor’s degree, in Biology or related scientific discipline. Exp: One to two years' |
The Research Associate II performs routine and complex laboratory tasks and procedures relevant to custom products and services in the Custom Technology Team. The Associate will perform a variety of routine experimental protocols and procedures to fulfill custom manufacturing requirements that include, but are not limited to formulations, experimental design, product testing/analysis, and results reporting. The Associate will work independently within generally defined procedures and practices in selecting methods and techniques for obtaining results. | 10/30/2021 |
| 7795 | Becton Dickinson Tempe, AZ Analytical Chemist Bachelor’s degree in Chemistry or related discipline Exp: 1-3 years |
Primary focus of position is chromatographic analysis, dissolution analysis, and wet chemistry of incoming materials and drug products. This includes following SOPs to perform routine lab functions such as in process and finished product testing for research and development and manufacturing operations. Assist with method development and validation activities to support product development activities. Plan and execute test method revisions. | 10/30/2021 |
| 7796 | Becton Dickinson Baltimore, MD QM Associate Scientist Bachelor's Degree in Biology, Microbiology or other related field Exp: 1-2 years' |
The QM Associate Scientist is responsible for applying basic scientific principles to routine laboratory work and for gaining experience in the application and interpretation of the department procedures. | 10/30/2021 |
| 7797 | Becton Dickinson San Diego, CA Research Associate - Molecular Point-of-Care BS or BA degree in Molecular Biology, Chemistry, Biochemistry, Bio/Biomedical Engineering, or related field Exp: 1 year |
BD is seeking a Research Associate to work within a team that develops new point-of-care assays for human in vitro diagnostic use, using nucleic acid isolation, amplification, and detection technologies. The Research Associate will assist in the design, development, integration, and qualification of assays and/or specimen processing workflows. The associate applies laboratory, scientific, and analytical skills to complete experiments. Works under the direction of Senior Scientists, Staff Scientists, Sr. Staff Scientists, or above. | 10/30/2021 |
| 7798 | Becton Dickinson San Diego, CA Reagent Scientist I - Molecular Point-of-Care BS or BA degree in Molecular Biology, Chemistry, Biochemistry, or related subject area. Master’s degree preferred. Exp: 1 year |
BD is seeking a Reagent Scientist I to work within a team that develops new point-of-care assays for human in vitro diagnostic use. The Reagent Scientist I supports various R&D assay development teams and is principally responsible for the formulation, organization, and quality control of assay raw materials, amplification master mixes, buffers, and consumables. The associate applies good laboratory practice and analytical skills to lead the overall reagent inventory, and material output and works with other team members to resolve technical challenges. Works under the direction of Senior Reagent Scientists or above. | 10/30/2021 |
| 7799 | Becton Dickinson San Diego, CA GC Chemist I B.S. Degree in Chemistry, Engineering, or Life Science Exp: 1 year |
The Quality Control Chemist I conducts various analytical testing of raw materials, semi-finished intermediates, finished products, and new compounds/products in various stages of design and development to characterize and determine quality. | 10/30/2021 |
| 7800 | Becton Dickinson Hunt Valley, MD QM Associate Scientist Bachelor's Degree in Biology, Microbiology or other related Life Science Exp: 1+ years' |
The QM Associate Scientist is a laboratory Microbiologist who independently schedules and performs a wide variety of multiple, complex microbiological tests of complex biological raw materials and greater than 100 different complex products in response to customer demand. The QM Associate Scientist performs data analysis using visual, instrumented, graphical and calculative means based on the biochemical, selectivity and growth promoting properties of media, In addition, the QM Associate Scientist assures that documentation and procedures are followed, updated and maintained as required by internal Quality Policies and related FDA/GMP guidelines. The QM Associate Scientist performs non-routine detailed project support and investigational testing and is involved in resolution of technical issues related to microbiological processes. | 10/30/2021 |
| 7801 | Be Biopharma Kendall Square, MA Research Associate / Sr Research Associate, Cell Therapies BS/MS in Cell and Molecular Biology, Bioengineering, Immunology or a related field Exp: 1+ years |
We re looking to hire a Sr / Research Associate to join our Cell Engineering team. We are looking for highly motivated, experienced, and innovative thinkers to join our growing team of passionate researchers to leverage B cells as a novel class of cellular medicine. This is an exciting opportunity to be part of a foundational team and help build Be Bio! | 10/30/2021 |
| 7802 | Be Biopharma Kendall Square, MA Research Associate / Sr Research Associate, NHP; Oncology Therapies Master’s Exp: 1+ years |
Help to establish protocols around differentiation of primary immune cells, including extensive tissue culture work (maintenance, expansion, and banking) Handling and analyzing workflows pertaining to cellular differentiation and profiling with downstream qRT-PCR, protein quantification, and other molecular readouts | 10/30/2021 |
| 7803 | Bethyl Laboratories, Inc. Montgomery, TX Laboratory Associate, Manufacturing Bachelor’s or Associate’s degree in Scientific field required Exp: 0-2 years |
The Lab Associate is responsible for stocking the lab, producing small- & large-scale material, and maintaining a clean work environment to ensure maximum productivity. The successful candidate is detail-oriented, highly motivated, and willing to develop new processes where they do not exist. | 10/30/2021 |
| 7804 | Bicycle Therapeutics Lexington, MA Research Scientist / Associate - Immuno-oncology B.S./M.S. Exp: 1-5 years |
The Research Scientist / Associate, Immuno-oncology will be primarily responsible for the development and execution of essential in vitro and ex vivo assays of systemic and tumor-targeted immune cell agonists to enhance progress of Bicycle’s oncology pipeline. In this role, he or she will be a key player in implementing the in vitro characterization of our immune modulators. | 10/30/2021 |
| 7805 | BigHat Biosciences San Mateo, CA Research Associate Undergraduate or Masters degree in biological sciences Exp: 1+ years |
BigHat Biosciences is seeking a self-motivated individual for a Platform Technician role to operate BigHat’s high-throughput, automated platform for producing and characterizing antibodies. | 10/30/2021 |
| 7806 | Shockwave Medical Santa Clara, CA R&D Engineer II (Clinical Engineering) Master’s Degree in Mechanical or Biomedical Engineering Exp: 1 year |
The R&D Engineer II will use technical skills in the development of innovative products to treat peripheral, coronary, and heart valve diseases. The R&D Engineer II will participate on multiple cross-functional development teams that manage projects from concept through commercialization. | 10/19/2021 |
| 7807 | Akorn Vernon Hills, IL Formulation Scientist Bachelor's Degree in Pharmaceutical Sciences or related field. Exp: one year |
We seek self-motivated, talented Formulation Scientists at various levels to join our expanding R&D team who will be responsible for developing the final product formulation, process procedures and packaging of semisolids, suspensions and solutions, lotions, nasal sprays, inhalations, sterile injectable and ophthalmic products etc. | 10/19/2021 |
| 7808 | SQZ Biotech Watertown, MA Research Associate, Exploratory Immunology BS in relevant scientific field. Exp: 1+ years |
We are seeking a highly motivated Research Associate to join the Exploratory team, the early-stage research arm of SQZ Biotech. The successful candidate will have a passion for early stage, creative, high-impact projects, with an ability to work both collaboratively and independently. | 10/19/2021 |
| 7809 | SQZ Biotech Watertown, MA Biomedical Associate Engineer Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Bioengineering, or related field. Exp: 0-6 months |
SQZ Biotechnologies is seeking a highly motivated and collaborative individual to join our Engineering group as a Biomedical Associate Engineer. The successful candidate will support the development of SQZ technology and manufacturing platform and collaborate with different teams to design and build custom cell therapy process equipment. | 10/20/2021 |
| 7810 | Talaris Therapeutics Louisville, KY Cell Processing Associate I Bachelor’s degree in related field of Science. Exp: 6 months |
A Cell Processing Associate I, to be based in Louisville, KY is a production professional responsible for the day-to-day operations related to clinical cell therapy manufacturing in a GMP and GTP compliant ISO 7 classified cleanroom facility. The primary responsibilities of this role focus on cell processing; secondary responsibilities include development and programmatic organization activities. | 10/20/2021 |
| 7811 | Talis Biomedical Chicago, IL Research Associate, Assay Development BS or equivalent in Molecular Biology, Biochemistry, Biomedical Engineering, Biochemical Engineering, Chemical Engineering, or a related field. Exp: 0-3 years |
We are seeking a highly motivated, talented, and driven Research Associate to join the Assay Development group in the R&D division at Talis Biomedical. This is a great opportunity to join a collaborative and dynamic team effort to enable development of rapid point of care diagnostic tests. The successful candidate will work in product development, including verification and validation activities. You will author, review, and edit SOPs, study protocols, reports and other documentation as needed. You will work collaboratively with others in Assay Development and other departments at Talis, including Assay Research, Operations, Quality, and Engineering. A strong understanding of nucleic acid biochemistry and experience working on cross-functional teams is highly desired. | 10/20/2021 |
| 7812 | Trevigen [Bio-Techne] Minneapolis, MN Research Associate, Conjugation Bachelor’s degree in chemistry, biological sciences or equivalent (chemistry or biochemistry preferred) required. Exp: 0 to 2 years |
This position is responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel. | 10/21/2021 |
| 7813 | Trevigen [Bio-Techne] Minneapolis, MN Research Associate Bachelor’s degree in a science related field; Or Masters degree in a science related field. Exp: 0-3 years |
We are now seeking a Research Associate at our Bio-Techne headquarters in Minneapolis to assist within one of our many business units that are producing and manufacturing high quality proteins, antibodies, immunoassays (like ELISAs, Luminex) and so much more. | 10/21/2021 |
| 7814 | Trevigen [Bio-Techne] Minneapolis, MN Research Associate, Quality Control Bachelor’s degree in a related field. Exp: up to 3 years |
This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 10/21/2021 |
| 7815 | Trevigen [Bio-Techne] Boston, MA Research Associate B.S. or M.S in Biology, Biochemistry, Molecular Biology, Immunology, Bioengineering or related discipline. Exp: 0-2 years |
We are looking for an individual who is highly motivated by our mission and technology, is self-organized, and is flexible to support a range of project within a fast-growing organization. | 10/21/2021 |
| 7816 | Trevigen [Bio-Techne] Minneapolis, MN Research Associate for Immunoassay Reagent Equivalence and Qualification Position requires a bachelor’s degree in Biology, Biochemistry or equivalent. Exp: 0 to 2+ years |
This entry to mid-level position is a >75% bench-based position that will execute antibody, protein, and raw material equivalence testing across multiple immunoassay platforms. This will ensure Bio-techne continues to have superb lot-to-lot consistency and prevent supply disruptions to ensure customer satisfaction. Plan and perform appropriate experiments, and report final conclusions with guidance from senior associate(s) and/or supervisor. This position functions collaboratively with multiple departments. | 10/21/2021 |
| 7817 | Unity Biotechnologies South San Francisco, CA RESEARCH ASSOCIATE 1/2, IN VIVO PHARMACOLOGY Bachelor’s degreeor a Master’s degree in biology, physiology, bioengineering or related field. Exp: BS 1-4 years; MS 1-2 years |
We are seeking to hire an exceptional Research Associate to join the in vivo pharmacology team. This position will be a critical part of a highly dynamic scientific research group supporting the characterization and development of drug candidates against novel drug targets. | 10/21/2021 |
| 7818 | Universal Cells Seattle, WA Research Associate I/ Associate II, Core Technologies in Seattle, Washington RA I: BS Degree; RA II: MS Degree Exp: BS 0-3 years; MS 0-2 years |
The primary purpose of a Research Associate I for our Core Technologies Department is to contribute to the further molecular engineering for our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to culture pluripotent stem cells as well as run molecular and cellular assays to characterize our proprietary Universal Donor Cells. | 10/21/2021 |
| 7819 | Universal Cells Seattle, WA Research Associate II, Immunology in Seattle, Washington MS Degree Exp: 0-2 years |
The primary purpose of the Research Associate II is to conduct research focused on generating and characterizing cells derived from pluripotent stem cells. This position will work primarily in a laboratory setting with a lead Scientist and R&D teams. | 10/21/2021 |
| 7820 | Universal Cells Seattle, WA Research Associate I, R&D in Seattle, Washington BS degree Exp: 0-3+ years |
The primary purpose of the Research Associate I position is to assist with the culture, gene editing, and differentiation of pluripotent stem cells. This position will work primarily in a laboratory setting in collaboration with other scientists and research associates. | 10/21/2021 |
| 7821 | Universal Cells Seattle, WA Research Associate II, Vector Production in Seattle, Washington MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the further molecular engineering for our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to assist with Adeno-Associated Virus production and the development and execution of molecular assays to characterize our proprietary gene edited cells. | 10/21/2021 |
| 7822 | Vaxart South San Francisco, CA Research Associate BS or MS in Cell biology, Biochemistry, or related disciplines. Exp: 0-5 years |
The Research Associate is responsible for performing analysis to support process and formulation development activities. Additionally, this role will support analytical method development for cell-based infectivity and transgene expression assays. | 10/21/2021 |
| 7823 | ViiV Healthcare King of Prussia, PA Associate Scientist, Upstream Process Development Bachelor’s or Master’s degree in Bioprocess, Biochemical, ChE or related Biological Science. Exp: up to 2 years |
In this role, you will be a member of a highly skilled team of scientists and engineers responsible for development and optimization of cell culture processes. The team will have access to the latest technology in small-scale as well as large scale bioreactors and analytical instruments. Although predominantly lab-based, the role also involves important aspects of verbal and written communication and requires good organisation skills as well as a broad scientific knowledge of cellular metabolism and physiology. | 10/21/2021 |
| 7824 | WaVe Life Sciences Cambridge, MA Research Associate/ Associate Scientist, CNS Biology MS degree Exp: 1-2 years |
Wave Life Sciences (Wave) seeks an experienced and highly motivated biologist to join its research team in Cambridge, MA. This is an ideal position for an individual with a strong background in drug discovery and early drug development who thrives in a team-oriented, fast-paced, and cross disciplinary biotech environment. This candidate will contribute to all levels of in vitro and in vivo discovery research to support development of optimized nucleic acid therapies for CNS disorders. | 10/21/2021 |
| 7825 | WaVe Life Sciences Cambridge, MA Associate Scientist / Senior Associate Scientist - CNS Biology MS degree in Molecular biology, biology or a closely related scientific field. Exp: 1-2 years |
Wave is looking for a highly motivated Sr. Research Associate / Associate Scientist to join its CNS research team in Cambridge, MA. This is an ideal position for a Biologist with a strong background in drug discovery and early drug development who thrives in a team-oriented, fast-paced, and cross disciplinary biotech environment. This candidate will have a hands-on-role and will contribute to all phases of discovery research to support the development of optimized nucleic acid therapies for CNS disorders. In vitro models, including iPSC-derived neurons and other molecular and cell biology techniques, will be heavily utilized within projects. | 10/22/2021 |
| 7826 | Global [Alta Sciences] Everett, WA Pathology Associate Bachelor of Science (B.S.) or Bachelor of Arts (B.A.) preferred. Exp: 0 -6 months |
ALAT certification preferred. The Pathology Associate I will perform necropsies, tissue trimming and processing on all pathology related study materials as specified in company protocols and SOPs. | 10/22/2021 |
| 7827 | Frontage Exton, PA Associate Scientist, Pharmaceutical Analysis-Small Molecule B.S. in Chemistry or related discipline. Exp: 1-2 years |
Hands-on experience with HPLC, UPLC, GC, LC/MS, IC and Dissolution Testing. Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines Assists method development Performs method validation under supervision Reports and resolves any unexpected issues under supervision Complies with all relevant cGMP and/or GLP regulatory requirements while carrying out assigned studies | 10/22/2021 |
| 7828 | Frontage Exton, PA Associate Scientist / Scientist M.S. for Scientist; B.S./B.A. for Associate Scientist Exp: 1-5 years |
This is a technical scientific position within the Study Bioanalysis Team. The Study Bioanalysis Team is responsible for conducting bioanalytical methods related to large molecule biotherapeutic drug development across all therapeutic areas, spanning nonclinical studies to post-market clinical development. | 10/22/2021 |
| 7829 | Frontage Hayward, CA Associate Scientist, Bioanalytical Services large molecule B.S./B.A. Exp: 1-5 years |
Performs job duties with some supervision, with majority of interaction with direct supervisor and project team members. | 10/22/2021 |
| 7830 | Frontage Deerfield Beach, CA Associate Scientist - Genomics A.A. or B.S. degree with substantial coursework in chemistry, biology and mathematics. Exp: one or more years |
The Associate Scientist will be primarily responsible for shipping and receiving of client samples, receipt of materials, and performing experiments to periodically evaluate the performance of scientific equipment and reagents that are being used in the laboratory. The individual will also perform quality control (QC) evaluations of laboratory procedures and data integrity. | 10/22/2021 |
| 7831 | Frontage Exton, PA Scientist/Associate Scientist- Biomarker Scientist B.S. level or M.S. level; Associate Scientist- B.S. level Exp: S: 1+ year ; AS: 0 year |
Scientist/Associate Scientist aids in the development of bioanalytical methods. | 10/22/2021 |
| 7832 | Frontage Exton, PA Associate Scientist-Product Development-CMC Master’s degree in Pharmaceutical Sciences, Polymer Chemistry, Microbiology, or Chemical Engineering Exp: 0-4 years |
Perform assigned tasks per procedures compliant with cGMPs and participate in the clinical manufacturing of parenteral, ophthalmic, and other sterile dosage forms. | 10/22/2021 |
| 7833 | Inotiv West Lafayette, IN Pharmaceutical Analyst I Master’s degree in a relevant field. Exp: 1 years |
Support and participate in company initiatives as directed by senior management Carries out and performs multiple complex procedures using laboratory equipment, computer resources, and institutional libraries’ | 10/22/2021 |
| 7834 | Inotiv Boulder, CO IHC Research Associate I Associates or bachelor’s degree - preferably in Biology, Chemistry, or a related science. Exp: 1+ years |
Under the direct supervision of the IHC Manager, performs immunohistochemical (IHC), immunofluorescent (IF) and in situ Hybridization (ISH) staining and testing in accordance with established standards and procedures using an automated staining platform. Maintains accurate and detailed records of work performed and results generated. | 10/22/2021 |
| 7835 | Wugen St Louis, MO/San Diego, CA, MO Associate Scientist: In vitro BS/MS degree in biology, engineering or related. Exp: 1+ years |
Wugen Inc. is seeking exceptional and highly motivated candidates to join our growing R&D team in St Louis and San Diego. This scientist will work closely with fellow synthetic biology scientists to develop and evaluate the activity and efficacy of novel candidate cellular therapeutics. This candidate will be responsible for the execution and analysis of preclinical studies and will play a vital role in the translation of our novel cell therapies to the clinic. | 10/22/2021 |
| 7836 | Wugen St Louis, MO/San Diego, CA, MO Associate Scientist: In vivo BS/MS in immunology, biology, pharmacology, or related scientific discipline. Exp: 1+ years |
Wugen Inc. is seeking exceptional and highly motivated candidates to join our growing R&D team in St. Louis and San Diego. This candidate will be responsible for establishing and performing in vivo testing to guide the selection and development of cellular therapies using mouse models of cancer. | 10/22/2021 |
| 7837 | 1910 Genetics Cambridge, MA Research Associate - Biology B.S. or M.S. in Biology, Cell Biology, Molecular Biology, Biochemistry, Pharmacology, or equivalent. Exp: 0 – 3 years |
Executing high throughput screening (HTS) assays in strict accordance with the NIH NCATS Assay Guidance Manual Developing and validating HTS biochemical assays for characterizing the activity and selectivity of potential drug candidates | 10/22/2021 |
| 7838 | A2 Biotherapeutics Los Angeles, CA Research Associate - Translational Science Master’s degree in science including biology, immunology, biotechnology or a related discipline. Exp: 0+ years |
The Translational Science team is seeking a highly motivated Research Associate with experience in biochemistry, cell and molecular biology, immunology and/or assay development. This role will help to develop our patient sample analysis capabilities for our upcoming clinical trials. Tasks will involve, but not be limited to: DNA isolation, cell culture, T cell manipulation and characterization, and executing a variety of immuno- and cell-based assays. The successful candidate will join us at our research facility in Agoura Hills, CA and will work on cutting edge science in a dynamic, fast-paced and team-oriented environment. | 10/22/2021 |
| 7839 | Abbott San Diego, CA Research Associate B.S. in Molecular Biology/Biochemistry, or a closely related field Exp: one year |
We have an exciting opportunity for an Innovative Research Associate I – Assay Development within our Abbott Rapid Diagnostics business located at Carlsbad, CA. In this role, you will help expand test content on the ID NOW™ platform by designing, screening and optimizing novel assays as well as engaging in research activities focused on expanding the capabilities of the core technology. Now is an exciting time to join! | 10/22/2021 |
| 7840 | AbbVie Worcester, MA Associate Scientist I/II, Multi-specific Biologics Platform B.S./M.S. in Biology or other related field. Exp: BS 0-3+ years ; MS 0-2+ years |
The Biologics Drug Biology Group at AbbVie is seeking a highly motivated research scientist to join the Multi-specific Biologics Platform team. This position is located at AbbVie Bioresearch Center in Worcester, MA. The desired candidate will play an important role in supporting the multidisciplinary groups across AbbVie focused on developing therapies for Immunology, Virology, Neurology and Oncology diseases. | 10/22/2021 |
| 7841 | AbbVie Worcester, MA Associate Scientist II, In Vivo Antibody Discovery M.S. in Biology or other related field. Exp: 0-2+ years |
The Biologics Generation Group within Global Biologics is seeking a highly motivated research scientist to join the In Vivo Antibody Discovery team at AbbVie Bioresearch Center (ABC). The ABC site, based in Worcester, MA, offers a unique setting where Biologics drug discovery, development and manufacturing coexist in one location. Our team interacts with multidisciplinary groups across AbbVie focused on developing therapies for Immunology, Virology, Neurology and Oncology diseases. | 10/22/2021 |
| 7842 | AbbVie Worcester, MA Associate Scientist II/ Scientist I, Cellular and Molecular Biology MS in Biochemistry, Molecular Biology, Cell Biology, or a related discipline. Exp: 0-2+ years |
The Molecular Pharmacology group is seeking an associate scientist responsible for conducting in vitro studies on the characterization of drug candidate molecules and the validation of drug targets. | 10/22/2021 |
| 7843 | AbbVie Worcester, MA Associate Scientist II/Scientist, Analytical Development Associate Scientist II: MS degreed within Biochemistry, Chemistry, Analytical Chemistry, Biophysics (or related discipline). Exp: no experience |
AbbVie is searching for an experienced and highly motivated individual to fill an Associate Scientist II/Scientist I position in the New Modality Group of Protein Analytics Department at AbbVie Bioresearch Center in Worcester, MA. The Protein Analytics Department is responsible for qualification and execution of analytical methods and characterization studies to provide product and process understanding as well as analytical CMC management for development of AbbVie biopharmaceutical pipeline from discovery through commercial stages as well as life-cycle management. | 10/22/2021 |
| 7844 | AbbVie Cambridge, MA Associate Scientist II/Scientist I, In-vivo Masters in biology or related field. Exp: 0 - 2+ years |
AbbVie is seeking an experienced, hands-on in-vivo scientist to join the In Vivo Pharmacology team at the Cambridge Research Center in Cambridge, MA. This individual will be responsible for designing and executing in vivo studies to support Parkinson’s Disease drug discovery projects. | 10/22/2021 |
| 7845 | AbbVie North Chicago, IL Associate Scientist I/II, Specialty Genomics Technologies BS degree in Genetics/genomic or related field ; MS degree in Genetics/Genomics Exp: BS: 0 - 3+ years; MS: 0 years |
As part of the Specialty Genomics team within AbbVie’s Genomic Technologies (GTECH) organization, the Associate Scientist I/II will conduct wet lab experiments and generate high quality biomarker and discovery data sets in support of pre-clinical and clinical molecular investigations. The Associate Scientist I/II will utilize specialty genomic technologies and collaborate directly with Senior Scientists within the GRC as well as with project stakeholders across AbbVie’s research and development and clinical development organizations. | 10/22/2021 |
| 7846 | Allergan Boston, MA Associate Scientist II - Foundational Immunology Master's degree Exp: 0+ (MS) years |
The Foundational Immunology Department is committed to advancing drug development through the deeper understanding of disease facilitated by deep molecular profiling. The Associate Scientist will be responsible for developing and implementing new technologies to enable immuno-profiling of disease from human samples and preclinical models. The successful candidate will have a strong background in molecular biology and immunology and a demonstrated ability to design, execute, troubleshoot, and interpret experiments independently. The successful candidate will have expertise in molecular techniques such as RNA isolation, RNA analysis by qPCR, experience with RNA Sequencing workflows and extracellular vesicle analysis. The ability to work as a part of a multi-disciplinary team, represent program-related work to senior management and external collaborators will be required. | 10/22/2021 |
| 7847 | Allergan Worcester, MA Associate Scientist II, Antibody Production MS in biology or related field Exp: 0-2+ years |
The Biologics Generation Group at AbbVie is seeking a highly-motivated research scientist to join a dynamic team supporting biologics drug discovery. This position will impact projects through purification and characterization of biopharmaceutical products such as monoclonal antibodies in high throughput. The ideal candidate should have direct experience with mammalian tissue culture, molecular techniques, and binding assays, such as ELISA and flow cytometry. Other desirable skills include protein purification expertise, proficiency in standard chromatography techniques, and protein characterization (e.g., MS, SEC). The applicant should be able to analyze, document, and report data. She/he should possess excellent communication skills and be comfortable presenting in group settings. | 10/22/2021 |
| 7848 | Allergan Waco, TX Laboratory Technician III, Microbiology Bachelor’s (B.S./B.A.) Degree in Microbiology or the Sciences. Exp: One (1) year |
Performs microbiological testing on raw materials, in-process and finished product samples. | 10/22/2021 |
| 7849 | AbSci Vancouver, WA Research Associate I/II/Sr., Synthetic Biology Master's degree in Molecular Biology, Biochemistry, Microbiology, or a related discipline. Exp: 1-2 years |
We are currently seeking a self-motivated and dedicated Synthetic Biology Research Associate/Senior Research Associate with a background in molecular biology, strain engineering, or synthetic biology to join our team. This person will be part of the Synthetic Biology R&D team and support the development of novel strains and technologies for efficient protein production using Absci's proprietary E. coli expression platform. Main responsibilities include molecular cloning and other molecular biology methods, preparing culture media, and strain engineering. The successful candidate should be capable of working with a high degree of independence. | 10/22/2021 |
| 7850 | Absorption Systems San Diego, CA In Vivo Research Associate Bachelor's degree in pharmaceutical sciences, life sciences, or pharmacology. Exp: 1-3 years |
The Research Associate position requires a broad knowledge of anatomy, physiology and biochemistry to help develop and support in vivo models to screen therapeutics and devices being developed for various disorders. Experience with surgical, dosing and sampling techniques is required. Prior experience working with other in vivo models may be considered even if there is no direct experience working with medical devices, stem cells or ophthalmology. | 10/22/2021 |
| 7851 | Absorption Systems Medford, MA Research Associate BS in a scientific field. Exp: 0-3 years |
The Research Associate I will work as part of a team in a lab environment to complete client-driven projects. | 10/22/2021 |
| 7852 | Absorption Systems San Diego, CA Research Associate Bioanalytical Bachelor's degree in chemistry, biochemistry or related discipline. Exp: 0-1 Year |
The Research Associate, Bioanalytical will provide support for bioanalytical quantitative analysis of test compounds in biological matrices obtained from a variety of studies including preclinical safety evaluations and pharmacokinetic evaluations. Focus on small molecule analysis using LC-MS/MS in support of drug discovery and early development programs. | 10/22/2021 |
| 7853 | Adimab Lebanon, NH Research Associate - Mass Spectrometry B.S. in analytical chemistry, biochemistry, or related fields Exp: 0-2 years |
We are seeking an eager-learning worker with a background in biochemistry, biophysics, analytical chemistry or related concentrations to join our Protein Analytics team. The Research Associate will work in a small team setting to support Adimab’s novel antibody discovery, optimization, and characterization workflows. This role will closely interface with the Antibody Engineering, Antibody Sciences, High-Throughput Expression, and Molecular Core teams. | 10/22/2021 |
| 7854 | ADMA Biologics Boca Raton, FL Chemist I B.S. in Chemistry, Biochemistry, Molecular Biology or related science discipline. Exp: 0-3 years |
The Chemist I will Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. | 10/22/2021 |
| 7855 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree/MS degree in Biological Sciences Exp: 1-3 years |
Preparing solutions and reagents for performing assays on the bench Perform Next Generation Sequencing-based genomic assays on different workflows | 10/22/2021 |
| 7856 | Patheon [ThermoFisher Scientific] Frederick, MD QC Scientist MS Degree in biochemistry, chemistry, molecular biology, or related degree. Exp: 1-2 years |
Plans and performs quality control testing of reagents and kits utilizing the Ion PGM Dx System. Collects and analyzes data for final disposition using preapproved documentation as well as troubleshoots assays. Participate in QC Method Validation and Method Transfer activities Participate in stability study activities | 9/29/2021 |
| 7857 | Patheon [ThermoFisher Scientific] Carlsbad, CA Protein Manufacturing Associate Master’s degree in Biology, Chemistry, Biochemistry, or other related discipline. Exp: 1+ years |
The successful candidate demonstrates a sense of urgency, contagious optimism and a “can do” attitude. They lead by example and hold themselves and others accountable, while maintaining productive and professional relationships within the team. | 9/29/2021 |
| 7858 | Patheon [ThermoFisher Scientific] St Louis, MO QC Support Scientist I Bachelor’s degree in a Biological Science or related field. Exp: 1 year |
This position supports the QC Analytical team for our Biologics Division in St. Louis, MO. As part of the Quality Control Analytical group, you directly impact patients’ lives by providing testing to ensure their biologic pharmaceuticals are safe and potent. | 9/29/2021 |
| 7859 | Patheon [ThermoFisher Scientific] Greenville, NC QC Scientist I (12-hr Nights) Bachelor’s degree in related discipline preferred. Exp: Up to 2 years |
Perform Environmental Monitoring in support of production activities in classified areas. Job function includes aseptic technique including aseptic gowning and working in cleanrooms to monitor the area while sterile products are filled and manufactured. This is a 12-hour night shift position, 6p – 6a, on a 2-2-3 schedule. | 09/29/2021 |
| 7860 | Patheon [ThermoFisher Scientific] Carlsbad, CA Scientist I, Microbiology A Bachelor’s degree in Life Sciences or Chemical/Biological Engineering. Exp: one year |
This position will work in the cGMP compliant QC Microbiology Laboratory supporting manufacture of biological products. Responsibilities include performing and providing support for functional aspects of the facility such as environmental monitoring (EM), microbiological testing (bioburden, bacterial endotoxin testing, growth promotion, biological indicators, stock cultures), media fills, water testing and validation support. | 09/29/2021 |
| 7861 | Patheon [ThermoFisher Scientific] Pleasanton, CA Scientist II, Molecular Biology MS in life sciences. Exp: 0-3 years |
You will be an active member of the R&D team with the ability to contribute to multiple R&D projects simultaneously. This is a hands-on scientist role. You are a self-starter, organized, and be highly motivated. The ideal candidate will have experience in developing and launching products. You will execute experiments systematically and maintain documentation include data traceability such that quality products can be made in accordance with the agreed timelines. You will actively contribute to feasibility, optimization, development and V&V activities in an R&D environment launching products with a purpose to grow our business. You may also collaborate with product transfer scientists across sites and also work with external collaborators. | 09/29/2021 |
| 7862 | Pillar Biosciences Natick, MA Research Associate B.S. or M.S in Biology, Molecular Biology, Genetics or related field. Exp: 1-3 years |
The Research Associate conducts research projects within well-defined guidelines, keep abreast of current publications relative to methods, techniques and developments within the field, evaluate results and summarize data collected and assists with and conducts laboratory experiments on research projects under the direction of senior lab personnel. | 09/29/2021 |
| 7863 | Poseida Therapeutics San Diego, CA Research Technician or Associate, Nanoparticle Formulations BS or MS with in pharmaceutical sciences, bioengineering, chemical engineering, chemistry, or related discipline. Exp: 0 to year years |
Poseida is searching for an outstanding Research Technician or Research Associate to join our Nanotechnology group. This position offers an exciting opportunity to develop non-viral delivery tools for gene editing and gene therapy applications. This person will be engaged in execution of formulation discovery experiments directed toward discovering and developing novel nanoparticle systems for delivering nucleic acids and proteins. | 09/30/2021 |
| 7864 | Poseida Therapeutics San Diego, CA Research Technician or Associate, In Vivo (Nanotechnology) BS or MS in biology, molecular/cell biology, or pharmacology. Exp: 0 to 3 plus years |
Poseida Therapeutics, Inc. is searching for an outstanding Research Technician/Associate to join our nanotechnology team. This position offers an excellent opportunity to develop delivery tools for gene therapy applications in an exciting and dynamic environment focused on cutting-edge gene editing technology. This person will be engaged in in vivo activities directed toward discovery and characterization of novel nanoparticle and other proprietary systems for delivering nucleic acids and proteins for in vivo gene therapy. | 09/30/2021 |
| 7865 | PTS Diagnostics Indianapolis, IN Scientist Master's degree Microbiology, Biochemistry, Chemistry, Biology, or other related discipline preferred. Exp: 1-3 years |
The Scientist will support the new product development programs for PTS Diagnostics and Sinocare. The ideal candidate will have a proven academic and industry track record. Scientist will deliver results in a fast-paced setting, and be a contributor to product development, method validations and scientific strategies. The Scientist works collaboratively with other scientists but is able to function independently with minimal oversight. | 10/01/2021 |
| 7866 | QurAlis Cambridge, MA Research Associate, Stem Cells Bachelor’s degree in the biological sciences or master’s degree. Exp: BS: 1+ year ; MS: 0-2 years |
QurAlis is seeking a highly motivated Research Associate to support and execute its cutting-edge discovery and screening efforts. The Research Associate will work closely with the QurAlis scientific and management teams to perform studies in a high quality and scientifically rigorous fashion. | 10/01/2021 |
| 7867 | Rakuten Medical San Diego, CA Cell Culture Associate - Upstream Cell Culture, Cell Line Development BS/MS Exp: >1 years |
Rakuten Medical is currently looking for a highly motivated individual to support cell line and upstream process development activities. This candidate will join Rakuten Medical ’s CMC team focusing on various aspects of preclinical antibody development including transfection and single cell cloning, cell culture process development, late-stage characterization, technology transfer and research material generation. | 10/01/2021 |
| 7868 | Rakuten Medical San Diego, CA Research Associate III, In Vivo Pharmacology M.S. Exp: 1+ years |
Rakuten Medical is searching for a highly motivated individual to support Rakuten Medical’s preclinical in vivo pharmacology team. The candidate will design and execute studies to evaluate efficacy and mechanism of action of hit and lead candidate products utilizing the most appropriate in vivo pharmacology models. This individual will participate and present data at weekly research meetings, and interface with other key functions such as TechOps. The successful candidate is also expected to train other members of the multidisciplinary research team in scientific, technical, and operational aspects of in vivo pharmacology. In alignment with the Rakuten Medical company culture, the individual will be expected to perform these duties in a highly collaborative manner with other members of the multidisciplinary research team, and will also have the opportunity to learn and grow in other functions. | 10/01/2021 |
| 7869 | MacroGenics Rockville, MD Manufacturing Associate I/II - Protein Purification Manufacturing Associate I - Bachelor’s degree in a related discipline; Manufacturing Associate II - Bachelor’s degree in a related discipline. Exp: MAI: no experience; MAII: one year |
The Manufacturing Associate I/II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Protein Purification area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 10/01/2021 |
| 7870 | MacroGenics Rockville, MD Manufacturing Associate I - Protein Purification Bachelor’s degree in a related discipline. Exp: no experience |
The Manufacturing Associate I participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Protein Purification area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 10/01/2021 |
| 7871 | MacroGenics Rockville, MD Manufacturing Associate II Bachelor’s degree in a related discipline. Exp: one year |
The Manufacturing Associate II/III participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 10/01/2021 |
| 7872 | ReGenX Biosciences Rockville, MD Associate Scientist/Senior Associate Scientist, Bioanalytical Sciences (PCR) A Bachelor’s or Master’s degree in a relevant scientific discipline. Exp: 1-2 years |
As a member of our Bioanalytical Sciences team, you will be responsible for developing and validating bioanalytical methods to support our gene therapy products pipeline. You will have the opportunity to collaborate with many different groups across the organization, including Research and Early Development, Quality, and Clinical Development and may oversee Contract Research Organizations to ensure that all applicable bioanalytical test methods are appropriate for the stage of non-clinical and/or clinical development. | 10/01/2021 |
| 7873 | Relay Therapeutics Cambridge, MA Research Associate, Genetic Diseases MS/BS Exp: 0 - 4 years |
In this role, you will design and execute molecular and cell biology experiments focused on evaluation of candidate molecules, and development of novel biomarkers. You will interact and collaborate cross-functionally with scientists in other departments, including biochemists, chemists, and computational and structural biologists while growing your understanding of drug discovery and helping bring medicines to patients. | 10/01/2021 |
| 7874 | Relay Therapeutics Cambridge, MA Research Associate, Discovery Technologies B.S./M.S. in Biochemistry, Molecular Biology, Structural Biology, Chemical Biology, or related field. Exp: 1+ years |
We are seeking a passionate laboratory Research Associate who can contribute to this initiative. You will use novel affinity-based screening techniques to generate the high-quality data needed to build our ML models and identify new ligands to challenging new targets. If you are passionate about working in the lab, making data-driven decisions and driving cutting-edge innovation, then we want you to join us! | 10/01/2021 |
| 7875 | Resilience San Diego, CA Research Associate, Genome Engineering B.S or M.S. in a biology-related field (e.g. molecular biology, genetics, synthetic biology, immunology, bioengineering). Exp: 0-2 years |
This role will be responsible for designing, performing, analyzing, and documenting experiments to support genome engineering research within Resilience R&D. They will work closely to assist scientists and engineers to develop and test workflows and hypotheses. The ideal candidate will have a proven track record of successfully carrying out laboratory SOPs independently. This role requires excellent verbal and written communication. | 10/01/2021 |
| 7876 | Rheos Medicines Cambridge, MA Scientist I, in vivo Biology M.S. in Immunology, Pharmacology, Animal Sciences or related fields of study. Exp: 1-3 years |
We are looking for a creative and motivated individual with hands-on in vivo/ex vivo experience with preclinical small animal models of autoimmune/inflammatory disease to join our Biology team. Working with the In vivo Lead, you will be supporting multiple programs at varying stages of development including target validation, late discovery, and IND-enabling studies. The successful candidate will be responsible for in vivo project support through model selection, experimental design and data analyses to define PK/PD relationships, biomarkers, and mechanism of action of target biology. | 10/01/2021 |
| 7877 | Rockland Immunochemicals Pottstown, PA Scientist I - Quality Control BA/BS in biochemistry, pharmacology, molecular biology, immunology, or related field. Exp: One year |
We are seeking a talented and highly motivated team player as an addition to our Quality Control (QC) Department. Join the group and apply your experience in the QC environment. | 10/01/2021 |
| 7878 | SCA Pharma Windsor, CT Microbiology Analyst I 4 year college degree Exp: 0-2 years |
As a Microbiology Analyst I, you will be responsible for supporting the Microbiology Department with data processing/entry, Environmental Microbiological testing and Filtration Testing, in addition to daily housekeeping of the laboratory. | 10/01/2021 |
| 7879 | Sebela Pharmaceuticals Roswell, GA QC Chemist Bachelor’s degree in Chemistry, or related discipline. Exp: 0-2 years’ |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. | 10/02/2021 |
| 7880 | Sherlock Biosciences Boston, MA Research Associate BS in Biology, Biochemistry, Bioengineering, or related discipline. Exp: 1+ years |
Assist in the development, verification, validation, and technology transfer of molecular diagnostic assays. Conduct laboratory experiments and studies according to approved protocols, Standard Operating Procedures (SOPs), and Work Instruction Documents (WIDs). | 10/02/2021 |
| 7881 | BioPharmGuy Anytown, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to do some data confirmation tasks. It can all be done on your computer. Even a few hours a week is fine. Must be able to accept payment via PayPal. If interested, send a message through the contact form. Thanks! | 9/25/2021 |
| 7882 | InVivoScribe San Diego, CA Manufacturing Associate I B.S. Degree in a scientific discipline. Exp: 1+ years |
We are looking to add a Manufacturing Associate I to our team for all aspects of production, including the production of master mixes, controls and assay kits. You will contribute to the drafting and review of new documents, including SOPs, Batch Records and Purchasing Specifications. | 9/21/2021 |
| 7883 | IsoPlexis Branford, CT Research Associate BS or MS in Biochemistry, Cell Biology, or a related field. Exp: 1 to 3 years |
Research and execute experiments to drive innovations in the IsoPlexis assay and microfluidic device Perform screening assays to characterize new antibody pairs for new immunoassays Developing and troubleshooting new immunoassays for commercialization Work with various types of immune and T-cells in various disease models, and perform analysis of impact upon interaction with stimulus and therapeutics ex vivo Assist with the investigation, creation and development of methods, experiments and / or technologies Recommends the design and implementation of procedures and protocols Execute assigned tasks following appropriate laboratory/technical procedures under minimal supervision | 9/21/2021 |
| 7884 | Vigene Biosciences Rockville, MD Manufacturing Associate I, Plasmid Production B.S. in Science or Engineering. Exp: < 1 year |
As a member of plasmid manufacturing team, the Manufacturing Associate I applies a broad knowledge of biological, bioprocess, and mechanical principles to execute manufacturing protocols in a regulated and controlled environment. Performs in-process analysis of plasmid production. | 9/21/2021 |
| 7885 | Vigene Biosciences Rockville, MD Quality Control Associate I - Materials Release Bachelor’s degree preferred but not required. Exp: 0-2 years |
The QC Associate I - Materials Release works in the Materials Release department to ensure that inventory used for manufacturing is sufficient to support multiple manufacturing processes. | 09/21/2021 |
| 7886 | Vigene Biosciences Rockville, MD Quality Assurance Associate I Bachelor of Science in Chemistry, Biological Sciences, Engineering, or related field, or equivalent experience. Exp: 0-2 years |
The Quality Assurance Associate I is responsible for performing various tasks within the department of Quality Assurance in accordance with current Good Manufacturing practices (cGMP). | 09/21/2021 |
| 7887 | Vigene Biosciences Rockville, MD Research Associate I, Plasmid Production B.S. in Biology, Cell Biology, Molecular Biology, or related fields, or equivalent experience. Exp: 0-2 years |
The Research Associate I is responsible for all aspects of bacterial culturing and DNA plasmid preparation, including organized record keeping and stock management. | 09/21/2021 |
| 7888 | Vigene Biosciences Rockville, MD Bioprocess Associate I, Upstream, Manufacturing Science & Technology B.S. in Chemical or Biomolecular Engineering, Cell Biology, Bioengineering, Biotechnology, or related field. Exp: 0-2 years |
The Bioprocess Associate I, Upstream, MS&T, will transfer product and process knowledge between development and manufacturing to ensure right-first-time clinical and commercial manufacturing and continuous improvement. Those processes include buffer and media preparation, upstream, and aseptic fill-finish. | 09/21/2021 |
| 7889 | Vigene Biosciences Rockville, MD Research Associate I, Upstream Process Development Bachelor of Science in Chemical & Bioengineering, Cell Biology, Biochemistry, Biotechnology, or related field. Exp: 0-2 years |
Under supervision, the Research Associate I will assist in executing experiments in cell culture, upstream related process assay, sourcing reagents, equipment, and materials for specific projects. | 09/21/2021 |
| 7890 | JGB Biopharma Consulting San Francisco Bay Area, CA Oncology Translational Scientist 1554 (Research Associate) BS / MS Exp: 1+ years |
Design and implement experiments necessary to provide in-vivo proof of biology evidence to advance the company’s drug candidates. Perform tumor model experiments to evaluate experimental drug through intravenous, subcutaneous, and intraperitoneal administration. Work with tissue cultures to prepare suspended tumor cell lines for implantation in mice Work with human T-cells to expand and characterize by Flow Cytometry Characterize tumor microenvironment by cell based assays and histological studies. Perform related in vitro experiments and analyze outcomes of pharmacokinetic, pharmacodynamic and efficacy studies Maintain accurate records and prepare / present results to other team members. | 09/21/2021 |
| 7891 | Charles River Laboratories Mattawan, MI Research Associate - Bioanalytical MS/BS/BA in relevant field. Exp: 0-2 years |
We are seeking a Research Associate for our Bioanalytical Department located in Mattawan, MI. The Research Associate is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others.We are seeking a Research Associate for our Bioanalytical Department located in Mattawan, MI. | 09/21/2021 |
| 7892 | Charles River Laboratories Reno, NV Research Assistant 1 - Laboratory Sciences - Starting at $22/hr with $750 sign on bonus. Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required. Exp: Zero to two years |
We are seeking a Research Assistant 1 for our Safety Assessment site located in Reno, NV. This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies.We are seeking a Research Assistant 1 for our Safety Assessment site located in Reno, NV. | 09/22/2021 |
| 7893 | Charles River Laboratories Mattawan, MI Research Associate - Immunology Bachelor’s/Master’s degree. Exp: 0-2 or more years |
A Research Associate is responsible for: quantifying, characterizing, synthesizing and/or modifying chemical entities according to applicable Standard Operating procedures (SOPs), established methods and/or GxP regulations. The individual in this role demonstrates proficiency in the use of applicable analytical and biochemistry instruments and laboratory techniques, and contributes to the team by completing assigned projects on time, contributing to process improvement initiatives, and communicating effectively with team members and customers. | 09/22/2021 |
| 7894 | Charles River Laboratories S. San Francisco, CA Research Associate, Bioanalytical 1 Bachelor's degree (B.S./B.A.) or equivalent in a scientifically related discipline. Exp: Minimum 6 months |
We are seeking a Discovery Bioanalytical Research Associate (DMPK Bioanalytical) for our Discovery site located in South San Francisco, CA. We are seeking Research Associate candidates that are early in their careers and are highly motivated, enthusiastic and possess a passion for learning. This position will be involved in all aspects of studies supporting the bioanalysis of drug molecules in multiple matrices. This position is ideally suited to recent graduates who enjoy a fast-paced and collegial environment. The individual in this position will be responsible for working hands-on and under the direction of more senior staff in a dynamic environment where teamwork, data quality, innovation and speed are valued. | 09/22/2021 |
| 7895 | Charles River Laboratories Frederick, MD Research Associate 1 - Report Coordination 1 1 Bachelor’s degree (B.S./B.A.) or equivalent in biology, zoology, chemistry, pathology or related field. Exp: 0 – 2 years |
We are seeking a Research Associate I for our Safety Assessment site located in Frederick, MD. Assist scientific staff by working under general guidance/supervision on basic scientific support, report development, regulatory compliance, and research. Knowledge, Skills, Abilities: Prepare protocols and amendments if applicable. Review study file for accuracy of scope of work prior to study initiation. Provide input to pathologists on workload prioritization. Assist pathologists with client communication, project tracking, and coordination. Monitor key study events including deliverables to client with guidance. Prepare basic tables for pathology reports. May perform image analysis with guidance. Assist with microphotography, whole slide scanning and/or radiography. Label, edit, arrange/organize, and print digital images. Assist in the preparation of pathology reports as directed by pathologists using basic templates. | 09/22/2021 |
| 7896 | Charles River Laboratories Skokie, IL Research Assistant 1/Research Assistant 2 EG Bachelor’s degree (B.S./B.A) or equivalent in a scientific related discipline. Exp: Zero to two years |
A Research Assistant 1 is responsible for performing moderately complex laboratory work in collaboration with departmental staff. Perform analysis of moderately complex laboratory assays based on protocols and in compliance with SOPs and GLP regulations. Record project data in accordance with GLP regulations. Set up basic laboratory equipment and instrumentation with guidance from senior technical staff. Adhere to current Health and Safety regulations. Perform all other related duties as assigned.We are seeking a Research Assistant 1/Research Assistant 2 for our Safety Assessment site located in Skokie, IL. | 09/22/2021 |
| 7897 | Charles River Laboratories Mattawan, MI Research Associate - Immunochemistry MS/BS/BA in relevant field. Exp: 0-2 years |
The following are responsibilities related to the Research Associate: This position is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others.We are seeking a Research Associate for our Immunochemistry Team site located in Mattawan, MI. | 09/22/2021 |
| 7898 | Leica Biosystems [Danaher] Port Washington, NY R&D Engineer I Bachelor's Degree in Mechanical/Biomedical/Materials/Polymer engineering or related field. Bachelor's Degree in Mechanical/Biomedical/Materials/Polym Exp: 0 – 3 + years' |
Support R&D’s goals by participating on the new product development team as a technical contributor on the design process: concept generation, optimization, feasibility, testing, validation, and transfer Builds prototypes and develops written test protocols to verify or evaluate design performance; executes evaluation and creates reports / presentations related to design activities Ensures product performance meets all specified requirements including regulatory Provides conceptual and detailed designs using CAD software, using tolerance analysis and stress calculations for design analysis Evaluates technical risks by leading or participating in DFMEA’s and ensuring accurate completion of required actions | 09/22/2021 |
| 7899 | Leica Biosystems [Danaher] SE Bothell, WA Associate Scientist, Chemistry R&D M.S degree in Chemistry or Biochemistry or similar science. Exp: 0-2 years |
This individual will be primarily responsible for performing a variety of oligonucleotide purifications to support early phase assay development teams achieve key milestones leading to design lock and eventual product commercialization. This individual will have cursorily operational competence of the MerMade and Shasta Synthesizer platforms. Additionally, the individual will have expert knowledge of Agilent analytical HPLC systems to perform oligonucleotide purifications and characterization, as well as quantitation of oligonucleotides via UV/Vis analysis. Expert operational experience of Thermo LTQ-XL high throughput mass spectral analyzer with intermediate level skills in the interpretation of the resultant spectra is expected. The Associate Scientist will support a variety of innovation teams and scientists within Bothell for multiple sub-projects that require specialty chemical skills. Post synthetic modification of oligonucleotides and characterization / analytical testing of complex biomaterials will be required. | 09/22/2021 |
| 7900 | Leica Biosystems [Danaher] Sunnyvale, CA Associate Scientist Master’s degree in field. Exp: 0-2 years |
This position is part of a New Product Development (NPD) team in the Biotechnology R&D department. The Associate Scientist position is primarily a bench level job focusing on technical studies required for assay development in an FDA-QSR and ISO9001 compliant organization. The ideal candidate will have experience in general molecular biology methods such as nucleic acid extraction and real-time PCR. This position requirements include experience with experimental design and good laboratory practices (GLP), scientific creativity and collaboration with cross-functional departments. In addition to technical qualifications, the ideal candidate will be highly organized and be able to thrive in an atmosphere of shifting demands and priorities. The candidate should possess excellent oral and written communication skills. The preferred candidate will have experience with Design Control and Product Development Processes.This position is part of a New Product Development (NPD) team in the Biotechnology R&D department. The Associate Scientist position is primarily a bench level job focusing on technical studies required for assay development in an FDA-QSR and ISO9001 compliant organization. | 09/22/2021 |
| 7901 | Leica Biosystems [Danaher] Cortland, NY Engineer I Bachelor’s degree in Mechanical Engineering. Exp: 0 – 5 years |
Performs research (biology, chemistry, mechanical, software, etc.) to generate analytical data for internal and/or external clients. Responsible for the investigation of new technologies and experimentation directed at the practical application of scientific theories. Assures that programs meet scientific objectives and are aligned with customer needs. Builds relationships with industry/technology key opinion leaders. 40% of the responsibilities - Engineering: design calculations, critical thinking and data analysis; creating design documentation and process instructions . 40% of the responsibilities - Product development/prototyping – lab testing, new product and process development 20% Project communication: meetings, collaboration, presentations, improving standard workPerforms research (biology, chemistry, mechanical, software, etc.) to generate analytical data for internal and/or external clients | 09/22/2021 |
| 7902 | Leica Biosystems [Danaher] Sunnyvale, CA Research Associate - FIT Bachelor’s degree in Biological Science field. Exp: 0-2 years |
The Research Associate is responsible for planning, executing, and discussing experiments that drive product development and sustainment. As a Research Associate, the employee has opportunities to learn Cepheid integrated platforms and technology with the goal of developing infectious disease tests to meet existing and emerging customer needs. Being a member of the Fast Impact Team (FIT), this role will execute activities that are in support of new product development (NPD) and business continuity strategies to ensure product availability and quality as demand increases in the market. FIT is an agile group of subject matter experts (SMEs) that can drop into a product family and develop, troubleshoot, or support post-launch investigations. This position is part of the Biotechnology R&D, Infectious Disease department and is located in Sunnyvale, CA. Our goal as a department, and as an overall organization is to understand the needs of our customers and to respond with accessible molecular diagnostic test systems as tools to improve the health and integrity of all communities. Our department is responsible for the active design of these systems with guidance from our leadership and multidisciplinary (i.e. interdepartmental) project core teams. | 09/22/2021 |
| 7903 | Leica Biosystems [Beckman Coulter Diagnostics] Miami, FL Manufacturing/Process Engineer I Bachelor’s degree in field. Exp: 0-2 years |
The Manufacturing/Process Engineer I for Beckman Coulter Diagnostics is responsible for determining the optimal manufacturing methods and process This position is part of the Miami Instrument Manufacturing department and will be located in Miami, FL. You will be a part of the Technical Operations team and report to the Manager of Process Engineering responsible for the design and implementation of manufacturing processes and equipment. If you thrive in a technical, fast-paced role and want to work to build a world-class engineering organization—read on.The Manufacturing/Process Engineer I for Beckman Coulter Diagnostics is responsible for determining the optimal manufacturing methods and process | 09/23/2021 |
| 7904 | PerkinElmer Richmond, CA Associate Clinical Scientist - Richmond CA Bachelor’s Degree in a physical science such as chemistry, biology, molecular biology or medical technology. Exp: 0-1 year |
PerkinElmer is seeking an Associate Clinical Scientist to join our team. Duties and Responsibilities: Prepares specimens for analysis and organizes tests to be performed. Prepares and properly labels reagents required for laboratory testing Conducts analysis of dried blood spots or body fluid to determine presence of normal and abnormal components. Reviews test results, maintains legible work records, and enters findings into the laboratory information systems. Performs routine preventative maintenance on instruments and equipment according to established schedule and procedure Verifies proper instrument function by checking and calibrating lab instruments and documents data. Records on instrument log any repairs, replacement and maintenance [performed on laboratory instruments. Abides by laboratory safety policies and procedures. The list of duties and responsibilities is not exhaustive and may be substituted as necessary | 09/23/2021 |
| 7905 | PerkinElmer Austin, TX Associate Lab Technologist BS degree in Life Sciences Exp: 0-3 years |
The Associate Lab Technologist will perform standard operating procedures applying basic laboratory techniques, calculations, materials measurement, operation of laboratory equipment, and record keeping necessary to manufacture and test life science reagents such as NGS and Food and Feed Safety products. Follow detailed instructions for assigned tasks or projects with direct supervision. | 09/23/2021 |
| 7906 | Jordi Labs Mansfield, MA Chemist Master’s degree in chemistry or other closely related field. Exp: one year |
Job duties: 1) Prepare technical reports 2) Interpret gas chromatograph mass spectrometry (GCMS) and liquid chromatograph mass spectrometry (LCMS) results with a high level of proficiency 3) Interpret chromatographic data including high performance liquid chromatography (HPLC), gas chromatography (GC), and gel permeation chromatography (GPC) results 4) Combine results from multiple techniques to identify unknown chemical compounds 5) Quantify chemical components using HPLC and GC results 6) Work with a team of scientists to design and implement analytical strategies 7) Perform or oversee complex analytical strategies with an emphasis of MS and chromatography 8) Review technical reports written by other scientistsJob duties: mance liquid chromatography (HPLC), gas chromatography (GC), and gel permeation chromatography (GPC) results | 09/23/2021 |
| 7907 | Kriya Therapeutics Redwood City, CA Research Associate I/II BS degree is Biochemistry, Chemistry, Molecular Biology or other science field with relevant course completion. Exp: RAI 0-1 years |
We are seeking a energetic candidate that will execute a range analytical techniques in support of AAV gene therapy method, process and formulation development. The position is heavily focused on benchwork and the applicant should have a desire to continue in a laboratory focused role. If you want to be a part of a fast paced start up company, please join us. | 09/23/2021 |
| 7908 | Krystal Biotech Pittsburgh, PA Research Associate– Downstream Process Development BS degree in Chemical Engineering, Biomedical Engineering, or Biological Sciences. Exp: 1 years |
A Research Associate position is available in the Downstream Process Development group. The successful applicant will have experience in laboratory research, and a desire to continue in a laboratory-focused role. This position will join a small team of scientists focused on developing and optimizing filtration and purification processes for recombinant viral vectors for early- and late-phase clinical trials. The Research Associate will be responsible for working with fellow scientists to develop robust, efficient, scalable strategies for improving process performance. | 09/23/2021 |
| 7909 | LakePharma Hopkinton, MA Research Associate, Pharma Assays and Analytics [JC-1424B] BS or MS in Biochemistry or related field. Exp: 1-5 year’s |
We are seeking a talented individual to join our team as a Research Associate, based in our Hopkinton, MA facility, supporting the Pharma Assay and Analytics group in the execution of R&D workflows. | 09/23/2021 |
| 7910 | LakePharma Hopkinton, MA Research Scientist, Pharma Assays and Analytics [JC-1400B] BS or MS in Biochemistry or related field. Exp: 1-5 year’s |
We are rapidly growing and seeking a self-motivated individual to join our Pharma Assays and Analytics team as a Research Associate. | 09/23/2021 |
| 7911 | LakePharma Worcester, MA Associate Scientist, Vector Technologies [JC-1484] BS in Biochemistry, Biology, or related. Exp: 1+ years |
We are searching for a talented individual to join our Vector Technologies Team as either an Associate Scientist. The successful candidate will be responsible for executing projects within the laboratory, writing study/research plans, and summarizing data to clients and colleagues via technical reports. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, as well as meeting or exceeding quality and timeline expectations. To be successful in this role, you must be organized, upbeat, and thrive in a fast-paced, innovative environment. | 09/23/2021 |
| 7912 | LakePharma San Carlos, CA Associate Scientist I [JC-1478] BS in Biology, Biochemistry, or related fields. Exp: 1-3 years |
We are rapidly growing and seeking a highly motivated individual to join our highly collaborative BioProduction team as an Associate Scientist. In this role you will perform laboratory bench work and technical services and report directly to our technical lead. The ideal candidate will think critically and creatively to help determine appropriate resources for resolution of problems. | 09/23/2021 |
| 7913 | Ligand Pharmaceuticals Durham, NC Associate Scientist, Cell culture/molbio Associate Scientist, Cell culture/molbio BS in biology or cellular/molecular biology. Exp: 0-2 years |
(we are looking to fill 2 positions under this job title) Icagen, part of the Ligand family of companies, is a biopharmaceutical company that partners with the pharmaceutical and biotechnology industry on drug discovery programs primarily focused on ion channel and membrane transporter targets. Icagen’s facility in Durham, North Carolina currently has an opening for a talented scientist to join our biology team. This is a full-time, laboratory-based position offering an opportunity to play key roles in identifying novel drug candidates and advancing drug development projects. The ideal candidate will have experience in a broad set of cellular and molecular biology techniques with a fundamental understanding of molecular biology. The successful candidate will be capable of managing multiple projects simultaneously while working as part of a core team. The work will be fast-paced and process-oriented in a dynamic environment which is predicated upon continuous improvement where everyone is encouraged to contribute to improving laboratory efficiency. | 09/23/2021 |
| 7914 | Locanabio San Diego, CA Research Associate, Stem Cell Biology BS in Biology, Biochemistry, Neuroscience, or related field. Exp: 1-2 years |
Locanabio is looking for a highly motivated individual with human stem cell experience to support the development and implementation of models that will contribute to our different Programs’ development. This position will be responsible for human iPSC culture, as well as implementation and characterization of monolayer (2D) and organoid (3D) differentiation models that will contribute to the identification and selection of new lead candidates, and optimal assays for therapeutic identification. This position will be responsible for assays that support research objectives provided by senior staff and may troubleshoot new strategic research directions, as necessary. You will have the opportunity to make significant contributions in our dynamic start-up environment where self-driven, enthusiastic employees thrive.Locanabio is looking for a highly motivated individual with human stem cell experience to support the development and implementation of models that will contribute to our different Programs’ development. | 09/23/2021 |
| 7915 | Mammoth Biosciences San Francisco Bay Area, CA Research Associate, Protein Discovery BS in molecular biology, biochemistry, or a related field. Exp: 1 year |
Mammoth is seeking a Research Associate with molecular biology and biochemistry expertise to join its growing Discovery team. The Discovery team is responsible for identifying and developing novel CRISPR-associated (Cas) nucleases for genome editing and diagnostic applications. The successful candidate will be responsible for executing laboratory workflows to develop Cas nucleases. They will have the opportunity to contribute broadly across multiple technical areas, including plasmid construction, NGS assays, protein purification, high-throughput screening, and laboratory automation. This is an excellent development opportunity for researchers who want to learn new skills and start their career working on cutting-edge CRISPR technologies.Mammoth is seeking a Research Associate with molecular biology and biochemistry expertise to join its growing Discovery team. The Discovery team is responsible for identifying and developing novel CRISPR-associated (Cas) nucleases for genome editing and diagnostic applications. | 09/23/2021 |
| 7916 | Mammoth Biosciences San Francisco Bay Area, CA Research Associate, Protein Purification BS in molecular biology, biochemistry, or a related field. Exp: 1 year |
Mammoth is seeking a Research Associate with experience in protein purification and biochemistry to join its Diagnostics team. This role will focus on nuclease development for diagnostic applications. The successful candidate will be responsible for executing laboratory workflows to purify and develop Cas nucleases. They will have the opportunity to contribute broadly across multiple technical areas, including protein purification, high-throughput screening, and laboratory automation. This is an excellent development opportunity for researchers who want to learn new skills and start their career working on cutting-edge CRISPR technologies.Mammoth is seeking a Research Associate with experience in protein purification and biochemistry to join its Diagnostics team. This role will focus on nuclease development for diagnostic applications | 09/23/2021 |
| 7917 | Mapp Biopharmaceutical San Diego, CA Research Associate I – Job #21-28A BA or BS or equivalent in a scientific related discipline. Exp: 1 year |
The Research Associate I will work in the ERDG which is responsible for isolating novel antibodies that may be used in future drug products. The Research Associate I is responsible for performing general laboratory duties as well as supporting ERDG laboratory personnel in meeting their research objectives. | 09/23/2021 |
| 7918 | MDxHealth Irvine, CA Laboratory Technician I (Shift: Monday to Friday 8:00am - 4:30pm) Bachelor's degree preferred. Exp: 1 to 2 years |
The Laboratory Technician I tasks will include specimen preparation, preparation and management of reagents and supplies, instrument preventive maintenance and troubleshooting and assisting in the performance of quality control procedures. | 09/23/2021 |
| 7919 | Mission Bio South San Francisco, CA Research Associate R&D B.S. / B.A. in Molecular Biology / Cell Biology / Biochemistry or associated fields. Exp: one year, preferably two years |
We are looking for a highly self-motivated individual to join the R&D Team as Research Associate. This exciting and challenging role is responsible for performing studies related to current and future product development. The position will be critical in generating analytical and experimental data related to Mission Bio’s products. | 09/24/2021 |
| 7920 | MOBILion Systems Philadelphia Area, PA Test Engineer Bachelor’s Degree in Electrical Engineering, Computer Science, or Physics Exp: 1+ years |
The Test Engineer will be responsible for developing test solutions that verify MOBILion’s products during development and in production. This includes analyzing requirements, creating and executing test plans, troubleshooting failures, as well as designing and maintaining custom hardware test systems. The Test Engineer will work closely with the engineering design teams to ensure systems and subsystems satisfy design requirements, and to implement any required test infrastructure. | 09/24/2021 |
| 7921 | Nanomix Emeryville, CA Research Associate Bachelor of Science (or foreign equivalent) in in Chemistry, Chemical Engineering, Biology, Bioengineering or related field. Exp: (3) months of experience in the job offer. |
Also requires three (3) months of experience in Analytical Techniques such as HPLC; Process Design and Optimization; and Experimental Design. Design and develop new cartridge prototypes, working with biosensors, filters, conjugate pads, microfluidics, device programming, etc. to enable specific biological assays on the eLab platform. Design processes required to manufacture product components by developing fixtures (CAD, Laser Printer, 3D Printer, Solidworks etc.), installing necessary components on machinery (Vacuum, Pressure Gauge, Pressure Regulator etc.), scripting robotic liquid handlers, drafting qualification requirements, and writing quality documentations. Design and execute biological wet lab experiments using ELISA, enzymatic assays, chromogenic assays, fluorescence/chemiluminescence. Work with electrochemical (CV, chronocoulommetry) and analytical (FTIR, Raman) tools to characterize biosensors and their performance. Develop quality control methods and implement them in the quality system. Perform large scale data analysis using JMP, PRISM, MATLAB, and Python to analyze research data and manufacturing data. | 09/24/2021 |
| 7922 | NanoComposix San Diego, CA Inorganic/Polymeric Nanoparticle Synthesis: Research Associate Masters degree in chemistry, biochemistry or nanoengineering or or minor in chemistry. Bachelors with at least 1 year experience in the field of nano Exp: MS - 0+ year; BS- 1+ year |
A nanoparticle synthesis Research Associate position is available at nanoComposix. Responsibilities include working with a team of Senior Scientists and Research Associates on various projects involving the synthesis and extended characterization of organic (PLGA) or inorganic (Metal, Silica) nanoparticles with a focus on biomedical applications. | 09/24/2021 |
| 7923 | NantKwest [ImmunityBio] Culver City, CA Research Associate, Molecular Biology BS in a scientific discipline Biochemistry, Biology, Chemistry, or another related discipline. Exp: 1 - 3 years |
ImmunityBio, Inc. (formerly NantKwest, Inc.) is developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. ImmunityBio Inc. is seeking a talented, motivated, and flexible Research Associate to assist with the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate will be a lab-based scientist and will work with a small team of research scientists. In this role, you will be an essential part of the molecular biology team to design, build, and assess constructs that support the discovery and development of therapeutics designed to treat human cancer. The successful candidate will possess excellent organizational skills and have strong attention to detail. | 09/24/2021 |
| 7924 | NantKwest [ImmunityBio] Culver City, CA Research Associate, Cell-Based Assays BS in a scientific discipline Biochemistry, Biology, Immunology, or another related discipline. Exp: 1 - 3 years |
ImmunityBio, Inc. (formerly NantKwest, Inc.) is developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. ImmunityBio Inc. is seeking a talented, motivated, and flexible Research Associate to assist with the discovery, research, and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate will be a lab-based scientist and will work with a small team of research scientists. In this role, you will conduct and interpret a diverse set of cell-based assays, including DNA and RNA transfection, flow cytometry, and cell proliferation to support the discovery and development of therapeutics designed to treat human cancer. The successful candidate will possess excellent organizational skills and have strong attention to detail. | 09/24/2021 |
| 7925 | NantKwest [ImmunityBio] Torrey Pines, CA Research Associate, Cell Culture Bachelor’s degree in Biology, Biochemistry, Immunology or a related field. Exp: 1-3 years |
The Research Associate (Cell Culture Technician) will assist scientist/senior research associate for the culturing, plating, distribution, maintenance, and banking of cell culture lines. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in an efficient, highly interactive, goal-oriented team environment, and working with minimal supervision. As a team member of the cell culture group you will work to support cell and tissue culture activities. The laboratory skills and training include expertise in mammalian cell culture, aseptic technique, sterile media preparation, tissue culture room maintenance, routine testing for endotoxin and mycoplasma. Also, contribute towards development of analytical methods for cell characterization. | 09/24/2021 |
| 7926 | NantKwest [ImmunityBio] El Segundo, CA Process Science Engineer l, Upstream Cell Culture Bachelors of Science in Chemical Engineering/bioengineering or related fields. Masters Degree preferred. Exp: up to 2 years |
ImmunityBio, Inc. is a late-stage immunotherapy company developing next-generation therapies that drive immunogenic mechanisms for defeating cancer and infectious disease. The company’s immunotherapy platform is designed to activate both the innate (natural killer cell and macrophage) and adaptive (T cell) immune systems to create long-term “immunological memory.” The Process Science Engineer will provide process development and engineering support for cell culture operations. The Engineer will work on process design, process improvements, scale-up and automation, tech transfers to GMP manufacturing, and process development for vaccine/gene therapy vectors. | 09/24/2021 |
| 7927 | NantKwest [ImmunityBio] El Segundo Nash, CA Manufacturing Associate, Fill Finish Bachelor’s Degree preferred. Exp: up to 2 years |
Who we are ImmunityBio, Inc. is developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. What you’ll be doing Responsible for the compliant execution of the fill and finish manufacturing processes strictly adhering to cGMP; environmental health and safety guidelines; and any other related regulations which could apply. Under the general direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. Activities include manual tasks and the operation of automated equipment.Who we are ImmunityBio, Inc. is developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. What you’ll be doing Responsible for the compliant execution of the fill and finish manufacturing processes strictly adhering to cGMP; environmental health and safety guidelines; and any other related regulations which could apply. Under the general direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. Activities include manual tasks and the operation of automated equipment. | 09/24/2021 |
| 7928 | NantKwest [ImmunityBio] 2 Locations: El Segundo; Culver Cit, CA Manufacturing Associate, Upstream Manufacturing Associate, Upstream BA/BS. MS preferred. Exp: up to 2 years |
Who we are ImmunityBio, Inc. is developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. What you’ll be doing The candidate is responsible for supporting Cell Culture manufacturing. All functions and roles of the Upstream manufacturing process are required to be performed with adherence to cGMP to ensure successful, quality operations. The candidate will also participate in cross-functional projects with Product Development (PD) and Process Engineering (PE) to develop, scale up and transfer new products. | 09/24/2021 |
| 7929 | Notable Labs Foster City, CA Overnight Research Associate BS/MS in cell biology, bioengineering, or related field. Exp: 6 months |
Are you looking for a mission driven company where your work will directly impact human lives? Do you think that cancer treatment should be personalized and want to build software to accelerate that reality? Notable Labs is a precision medicine company that has a translational drug discovery platform focused on identifying therapeutic options for relapsed and refractory cancer patients. table’s culture extends from it’s core mission of redefining treatment for hematological cancer patients. Our team of scientists and engineers are dedicated to this mission and take to heart that their work truly has an important impact. Whether it is processing fresh patient bone marrow samples, performing complex data analysis or maintaining our CLIA certification, we all work collaboratively so that new drugs may be discovered and treatment options improved. What you will do: As a member of a close R&D team, You will be supporting our numerous projects and be an integral part in scaling up for future upcoming projects Will be responsible for processing primary samples and preparing them for our automated high-throughput screens Operate and monitor our cutting edge automated laboratory screening system and software for our high throughput screening assay Support laboratory automation, perform scheduled instrument maintenance per SOP Qualify and re-qualify lab equipment for production use Identify any issues that may adversely affect the quality of test results and report to appropriate representatives to ensure prompt resolution **This is a salaried position that requires weekly overnight shifts. ** | 09/24/2021 |
| 7930 | Notable Labs Foster City, CA R&D Research Associate BS/MS in cell biology, bioengineering, or related field. Exp: 1 year |
Research Associate, R&D Assay Development What you will do: As a member of the R&D team, you will: Develop new endpoints for transformative ex vivo high-throughput screening (HTS) assays to assess the efficacy of different drug classes on primary human tumor samples Optimize assay conditions to support industry and academic partnerships Run HTS assays using cutting edge automated screening and software Work collaboratively with engineering, computational biology, high-throughput screening, business development groups Present data at group meetings | 09/24/2021 |
| 7931 | Pacific BioLabs San Francisco Bay Area, CA MICROBIOLOGY LABORATORY TECHNICIAN An undergraduate degree in a science-related field (e.g., Microbiology, Biological Sciences). Basic scientific knowledge demonstrated by previous cour Exp: 0+ years |
Local candidates (San Francisco Bay Area) preferred. PBL has an immediate opening for a full time Laboratory Technician in the Microbiology Department. The Laboratory Technician will report to Microbiology Management and will contribute to general laboratory testing, sample management, and laboratory maintenance. Primary responsibilities include but, are not limited to the following: Laboratory housekeeping tasks, collecting and processing laboratory test samples, perform equipment preventive maintenance, perform cleanroom preparation and maintenance, media preparation, environmental monitoring, maintenance of departmental logbooks and testing guidelines in accordance with SOPs and cGMP regulations. The Laboratory Technician is expected to participate with the team to meet Microbiology Department goals and perform routine laboratory duties as directed. PRIMARY RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO Ensuring laboratories are clean and safe (in compliance with cGMP) and properly stocked. Performing regular inventory of reagents, consumables and materials. Cleaning and maintaining laboratory equipment such as glassware, freezers, hoods, incubators and water baths. Performing dry goods and liquid media autoclave sterilization cycles. Maintaining overall laboratory organization that facilitates Study Director/Analyst ability to complete testing deliverables that includes sample preparation, QC data review, database entry and filing. Performing water and critical utility sample collection. Performing based laboratory testing such as TOC, Conductivity, HPC and pH. Performing Environmental Monitoring. Media preparation. Additional responsibilities related to job function. | 09/24/2021 |
| 7932 | Cytokinetics South San Francisco, CA Discovery Biology, Research Associate I/II Contract BS or MS in biochemistry, cell or molecular biology, physiology, or related field. Exp: 1-2 years |
We are currently seeking a Research Associate for our Discovery Biology department. As a Research Associate, you will thrive as a highly motivated and creative scientist! This is an exciting opportunity to be part of a growing, dynamic, and highly collaborative R&D team involving novel target approaches to find medicine for unmet medical needs! Our Research Associates collaborate with scientific mentors in a one-on-one reporting structure to support early discovery research and understand mechanism of action of molecules for evaluation as potential drug candidates for cardiovascular and neuromuscular diseases. You will collaborate with a broad group of highly qualified scientists and focus on advancing drug discovery research programs to the stage of clinical development. | 9/13/2021 |
| 7933 | Cytokinetics South San Francisco, CA Research Associate, Medicinal Chemistry BS/MS in Chemistry. Exp: 0-3 years |
We are currently seeking a Research Associate for our Medicinal Chemistry department. As a Research Associate, you will thrive as a highly motivated and creative scientist! This is an exciting opportunity to be part of a growing, dynamic, and highly collaborative R&D team involving novel target approaches to find medicine for unmet medical needs! Our Research Associates collaborate with scientific mentors in a one-on-one reporting structure to design and efficiently synthesize target molecules for evaluation as potential drug candidates. You will collaborate with a broad group of highly experienced scientists and focus on advancing drug discovery research programs to the stage of clinical development. | 9/13/2021 |
| 7934 | Cytokinetics South San Francisco, CA Contract Research Associate I - Sample Management BS degree. Chemistry or Biology related major preferred. Exp: 0-1 years’ |
We are seeking someone to join our Sample Management group as a Contract Research Associate I. You are joining a time of growth for the company and the Research team overall! This will be a tremendous learning opportunity to be working hands-on with an experienced group of researchers who want to help advance in your career! | 9/13/2021 |
| 7935 | CytomX Therapeutics South San Francisco, CA Research Associate II/Senior Research Associate, Analytical & Formulation Development M.S. in analytical chemistry, biochemistry, pharmaceutical development, biophysics, or related fields. Exp: 1-3 years |
We seek a highly motivated individual to join a collaborative, productive and dynamic team and provide analytical development support for advancing exciting CytomX clinical programs into late-stage development and commercial launch. The successful candidate will have ample opportunities for career development and growth. | 09/13/2021 |
| 7936 | CytomX Therapeutics South San Francisco, CA Research Associate II, Protein Sciences MS in Biochemistry Exp: 1 year |
We seek a highly motivated individual to participate in the purification and characterization of Probodies, various bispecific molecules (TCBs) and Procytokines to support all discovery and development programs at CytomX. The successful candidate will work as a Research Associate II in the Protein Sciences department. | 09/13/2021 |
| 7937 | Decipher Biosciences San Diego, CA Clinical Lab Technician Bachelor’s degree required. Exp: 1 years’ |
We are currently seeking a dynamic Clinical Lab Technician to join our team in San Diego. Innovator Profile The Clinical Lab Technician’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. | 09/13/2021 |
| 7938 | Decipher Biosciences San Diego, CA Research Associate I, Assay Development B.Sci. in biological sciences (or related field). Exp: 1-2 years |
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. | 09/13/2021 |
| 7939 | Deepcell Menlo Park, CA Research Associate/Senior Research Associate, Biology Bachelor’s degree or Master’s degree in bioengineering, molecular biology, cell biology, genetics, or similar field. Exp: BS - 1+ years’ |
We are looking for multiple research associates to join the biology team and help us to unlock the power of cell morphology and connect the genome to the patient. | 09/13/2021 |
| 7940 | Deepcell Menlo Park, CA Research Associate/Senior Research Associate, Biology Bachelor's degree or Master's degree in bioengineering, molecular biology, cell biology, genetics, or similar field. Exp: BS - 1+ years’ |
We are looking for multiple research associates to join the biology team and help us to unlock the power of cell morphology and connect the genome to the patient. | 09/13/2021 |
| 7941 | DewpointX Boston, MA Research Associate – Screening & Automation B.S. or M.Sc. in biochemistry, cell biology, biotechnology, or a related subject. Exp: 1-3 years |
We are looking for a creative, energetic individual to join our team as a screening and automation Research Associate, supporting high content/ high throughput assays and instrumentation for multiple disease areas. The successful candidate will be highly skilled in cell-based assay development and validation, in the context of high throughput screens. In this position you’ll be part of an energizing and supportive startup culture engaged in continuous learning, and part of an exceptional international team. This role is based at our site in Boston's Seaport district. Dewpoint offers competitive salary and benefits | 09/13/2021 |
| 7942 | DewpointX Boston, MA Research Associate/Sr. Research Associate – Oncology A BS or MS in molecular biology, biochemistry, biology, or affiliated scientific discipline. Exp: 0-2 years |
We are searching for a Research Associate/Sr. Research Associate to join our oncology efforts. You will help develop and execute experiments to dissect the role of condensates in oncogene regulation. Additionally, you will perform high-content imaging in disease-relevant cell models to validate condensate-cancer hypothesis and empower drug screening efforts. In this position you’ll be part of an energizing and supportive startup team culture, engaged in continuous learning, and part of an exceptional international team. This role is based at our site in Boston's Seaport district. Dewpoint offers competitive salary and benefits. | 09/13/2021 |
| 7943 | Diabetomics Hillsboro, OR Research Assistant/Associate in Product Development (2 positions available immediately) BA/BS in a relevant biological science. Exp: 1-2 years |
Diabetomics, Inc., is a leading medical diagnostics company serving the needs of personalized health and diabetes risk assessment and management. Diabetomics R&D group is currently seeking a Research Assistant/Associate to join our established team. Essential Functions: Supports the Diagnostic Product Development team. This is a hands-on, bench-level laboratory position. Tasks will include, but are not limited to: assay feasibility, assay development, optimization, reagent formulation, verification and validation studies. | 09/13/2021 |
| 7944 | Diabetomics Hillsboro, OR Quality Engineer bachelor’s degree in a technical or related field. Exp: 1-5 years |
The primary role is to maintain quality assurance throughout the organization, improving quality processes while maintaining or improving efficiencies. | 09/13/2021 |
| 7945 | Dicerna Pharmaceuticals Lexington, MA Research Associate, RNAi Discovery BS/MS in a relevant field Exp: 0-5 year’s |
Dicerna Pharmaceuticals is looking for a BS/MS scientist to help in its drug discovery efforts. This is a hands-on research position that requires strong expertise in molecular and cellular methodologies. This is a full-time position. Dicerna offers an exciting work environment and strong team culture. Our company has a competitive benefits package and bonus incentive program. | 09/13/2021 |
| 7946 | Dicerna Pharmaceuticals Lexington, MA Research Associate /Senior Research Associate – Translational Biology Bachelor’s or Master’s Degree in Biology, Pharmacology, or related field. Exp: 1-3 years |
We are seeking a highly skilled research associate to lead mechanism of action and pharmacology studies on Dicerna’s GalXC therapeutics. Major responsibilities include conducting in vivo studies on our pre-clinical and clinical candidates and conducting hands-on research. You will apply your expertise on animal dosing and surgery and deep understanding of the molecular and cellular biology to study liver diseases and play an important role in all phases of drug discovery and clinical development at Dicerna. | 09/13/2021 |
| 7947 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations B.S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 09/14/2021 |
| 7948 | DxTerity Rancho Dominguez, CA Research Associate B.S. or M.S Degree in Biochemistry, Molecular Biology or a related field. Exp: 1-3 years |
DxTerity, a patient-centric genomics company located in Los Angeles, CA is looking to hire a Research Associate to join our Research and Product Development team. Responsibilities include: development of molecular diagnostic test kits, reagents and procedures in a team environment. Perform experiments independently after receiving general direction from supervisor. Make detailed observations, analyzes data and interpret results. Prepare technical reports, summaries, protocols and quantitative analyses. Maintain and develop skills in molecular biology and company technology through reading of internal reports and scientific literature. Support the achievement of project objectives and time schedules while meeting ISO and FDA regulatory and design control requirements. | 09/14/2021 |
| 7949 | Encoded Therapeutics South San Francisco, CA Research Associate, In vitro Neurobiology Research Bachelors or Masters degree. Exp: 0-2 years |
Encoded Therapeutics is seeking a highly motivated senior research associate – in vitro neurobiology research, to join our Molecular and Cellular Pharmacology group. This individual will work closely with other members of the group to develop and execute on primary neuron culture procedures in support of program advancement, from target identification to preclinical proof-of-concept. The successful candidate will primarily conduct in vitro studies, and is expected to have strong experience with primary neuron culture from the rodent brain. | 09/14/2021 |
| 7950 | Encoded Therapeutics South San Francisco, CA Research Associate/SRA, Downstream Process Development RA position, MS in a chemical engineering, biochemical engineering, biochemistry or other relevant area. Exp: 1+ years |
This is a unique opportunity to work at the intersection of genomics and therapeutics and participate in the development of a diverse therapeutic pipeline driven by a transformative core technology. The position of Senior Research Associate will assist the Downstream Process Development group at Encoded Therapeutics. A qualified candidate will be responsible for purification process development and support purification of our lead program at small and pilot scales. The ideal candidate will be hardworking, flexible and able to perform key responsibilities across multiple projects in a fast-paced and dynamic environment. | 09/14/2021 |
| 7951 | Encoded Therapeutics South San Francisco, CA Research Associate/Senior Research Associate, Analytical Development For the RA position, MS in a relevant area of specialization (analytical chemistry, biochemistry). Exp: 1+ years |
Working closely with scientists to develop protein analytical methods including HPLC (SEC, IEX, RPLC), LC-MS (intact MS, Peptide mapping and proteomics) and CE Collaborate with cross-functional teams to support analytical development, process development and comparability studies. Operates under GDP, Good Documentation Practice for efficient data management and retrieval. Record experimental procedure and results accurately in laboratory notebooks Work on multiple projects to meet departmental and organizational goals. | 09/15/2021 |
| 7952 | Etubics [Immunity Bio] Torrey Pines, CA Research Associate, Cell Culture Bachelor’s degree in Biology, Biochemistry, Immunology or a related field. Exp: 1-3 years |
The Research Associate (Cell Culture Technician) will assist scientist/senior research associate for the culturing, plating, distribution, maintenance, and banking of cell culture lines. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in an efficient, highly interactive, goal-oriented team environment, and working with minimal supervision. As a team member of the cell culture group you will work to support cell and tissue culture activities. The laboratory skills and training include expertise in mammalian cell culture, aseptic technique, sterile media preparation, tissue culture room maintenance, routine testing for endotoxin and mycoplasma. Also, contribute towards development of analytical methods for cell characterization. | 09/15/2021 |
| 7953 | Etubics [Immunity Bio] Culver City, CA Research Associate, Molecular Biology BS in a scientific discipline Biochemistry, Biology, Chemistry, or another related discipline. Exp: 1 - 3 years |
ImmunityBio, Inc. (formerly NantKwest, Inc.) is developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. ImmunityBio Inc. is seeking a talented, motivated, and flexible Research Associate to assist with the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate will be a lab-based scientist and will work with a small team of research scientists. In this role, you will be an essential part of the molecular biology team to design, build, and assess constructs that support the discovery and development of therapeutics designed to treat human cancer. The successful candidate will possess excellent organizational skills and have strong attention to detail. | 09/15/2021 |
| 7954 | Etubics [Immunity Bio] Culver City, CA Research Associate, Cell-Based Assays BS in a scientific discipline Biochemistry, Biology, Immunology, or another related discipline. Exp: 1 - 3 years |
POSITION SUMMARY ImmunityBio, Inc. (formerly NantKwest, Inc.) is developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. ImmunityBio Inc. is seeking a talented, motivated, and flexible Research Associate to assist with the discovery, research, and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate will be a lab-based scientist and will work with a small team of research scientists. In this role, you will conduct and interpret a diverse set of cell-based assays, including DNA and RNA transfection, flow cytometry, and cell proliferation to support the discovery and development of therapeutics designed to treat human cancer. The successful candidate will possess excellent organizational skills and have strong attention to detail. | 09/15/2021 |
| 7955 | Evelo Biosciences Cambridge, MA Research Associate/Associate Scientist, Discovery and Immuno-Oncology BS degree or higher degree. Exp: 1 or more years |
Evelo Biosciences, Inc.(Nasdaq: EVLO) (“Evelo”), a biotechnology company developing monoclonal microbials, a new modality of oral biologic medicines is looking for a highly motivated individual who is energized by the prospect of working in a clinical- stage company, has a strong desire to learn, and wishes to function integrally as part of an interdisciplinary team. Evelo Biosciences is seeking an experienced In Vivo Research Associate/Associate Scientist to join our Discovery and Immuno-Oncology team. Evelo Biosciences, Inc. (Nasdaq: EVLO) is a biotechnology company developing new modalities of orally delivered, systemically acting biologics that could disrupt the industry. We aim to recruit a scientifically and technically exceptional in vivo researcher to play an important role in our team and contribute to our science. The successful candidate will be a highly motivated laboratory researcher who is energized by the prospect of working in a clinical stage company, has a strong desire to learn, and wishes to be an integral member of an interdisciplinary team. The ideal candidate will possess strong technical in vivo skills and the ability to execute independently. We are seeking highly motivated and curious individuals who have extensive hands-on experience performing in vivo and ex vivo studies using laboratory mice and dosing by various routes of administration, with some degree of understanding and experience in immunology and/or oncology, thus ready to multi-task within scope. | 09/15/2021 |
| 7956 | Facet Medical Technologies Atlanta, GA QUALITY ENGINEER BS in Engineering, Science or related technical field. Exp: 1-3 years |
Plans and directs activities concerned with development, application, and maintenance of quality processes, materials, and products. Additionally, responsible for investigation manufacturing and customer nonconformance’s, determining root causes and corrective actions, reviewing and approving protocols and final reports and developing product specifications and sampling plans. | 09/15/2021 |
| 7957 | Fate Therapeutics San Diego, CA Research Associate II / I, Translational Science B.S. degree in Biological Sciences/Molecular Biology or other related field. Exp: 1+ years |
Fate Therapeutics is seeking a motivated individual to join a growing Translational Science team in support of the company’s iPSC derived immunotherapy clinical trials. This position will support data documentation, DNA and RNA extractions from blood and tissue, PCR, clean-up of genetic material, and handling of human samples. The successful candidate will have a bachelor’s degree in molecular biology, and experience with molecular laboratory techniques. This is a full-time position reporting to a Scientist of Translational Science and is located at our corporate headquarters in San Diego, CA. | 09/15/2021 |
| 7958 |
Frontida BioPharm Philadelphia, PA Associate Analytical Scientist Master of Science in Chemistry or related major or a Bachelor of Science degree. Exp: MS 0-2 years’; BS 0-3 years’ |
We are seeking an Associate Analytical Scientist to join our Analytical Research & Development Team at our Philadelphia location. This is a laboratory-based position and the candidate will be responsible to support formulation development by performing method development, validation, writing protocols and reports, conducting chemical and physical testing activities for both ANDA and NDA projects. | 09/15/2021 |
| 7959 | Frontier Medicines South San Francisco, CA Research Associate / Senior Research, Platform Chemistry - South San Francisco Bachelor’s Degree (Research Associate); Master’s Degree in synthetic organic or medicinal chemistry, or to be completed within 6 months. Exp: BS - 0-3 years |
We are currently seeking an outstanding individual to join our team as Research Associate / Senior Research Associate, Platform Chemistry. The ideal candidate for this position will have a Bachelor’s or Master’s degree in Chemistry (or a related discipline, with synthetic chemistry experience), and is someone who is passionate about making an impact in drug discovery through chemical synthesis. The successful candidate will have a Bachelor’s- or Master’s degree and would be capable of starting work between Sept. ’21 and Jan. ‘22. In the titled role, one will have the opportunity to impact the expansion of Frontier’s proprietary chemistry platform and contribute to therapeutic programs throughout the organization. In this laboratory-based position, the successful candidate will partner with both internal and external medicinal chemistry teams to generate innovative solutions to accelerate lead generation and lead optimization efforts within the context of small molecule drug discovery projects. She/he will maintain close interactions with colleagues across interdisciplinary lines. Strong people skills and the ability to thrive in a team and goal driven environment are key attributes. This individual must also excel in communication and have strong interpersonal skills necessary to influence in a collaborative multidisciplinary environment. This position is located in South San Francisco. | 09/15/2021 |
| 7960 | Fujifilm Diosynth Research Triangle Park, NC Contract Associate Scientist, Upstream Process Development M.S./ B.S. Exp: 1+ years |
The Upstream Process Development group is seeking a Contract Associate Scientist with experience in microbial technologies. An Associate Scientist assists in conducting experiments for programs and works with the team to maintain the lab and equipment. The individual monitors on going experiments and can identify unusual occurrences. An Associate Scientist understands and applies knowledge within area of expertise and can take an active role in non-routine process development activities. This is a contract position that is expected to last approximately 12 months and includes benefits. | 09/15/2021 |
| 7961 | GenMark Diagnostics Carlsbad, CA Research Associate I, PTS M.S. degree in Biochemistry, Molecular biology or related field. Exp: zero (0) to two (2) years |
The Research Associate I will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision. An exciting career opportunity to work closely with cross functional teams to investigate root cause of anomalies reported during Quality Control or from Customer Technical Support. Responsible for planning, design, and execution of experiments for product and manufacturing improvements Conducts scientific experiments and troubleshooting activities with minimal guidance from manager or senior team member Conducts data analysis, interprets and reports results Quickly becomes familiar with manufacturing processes directly associated with assigned project Submits work orders and ensures clear communication with the cross functional team to drive troubleshooting and manufacturing process improvement projects Collaborate with customer technical support as needed May work with human specimens and infectious organism Experience with good documentation practices | 09/16/2021 |
| 7962 | GenMark Diagnostics Carlsbad, CA Research Associate I, Assay Development M.S. in Biochemistry, Molecular Biology, Analytical Chemistry or a related field. Exp: 0+ years |
The Research Associate I will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision. You will investigate, adapt or modify experimental methods and technologies for project advancement. A unique opportunity to leverage your background and skills in molecular diagnostics to enhance and build your career by working cross-functionally. An exciting career opportunity where your contributions will impact business opportunities through successful completion of projects. Responsible for day to day running of experiments and data analysis in the assay development laboratory Conducts general molecular biology tasks, including nucleic acid purification, quantification, amplification and analysis on multiple platforms Prepares reagents and solutions as needed, using appropriate procedural and documentation methods, including industry standard good laboratory practices Responsible for maintaining stockroom supplies and inventory Performs duties under supervision with increasing independence Identifies and solves problems in experiments or protocol designs, suggests improvements Prepares documents meeting company standards, including data summaries, reports, SOPs and procedures Presents work at meetings as required, and proposes new strategies and methods to address immediate and upcoming technical issues Reads literature directly associate with assigned project and related areas Interacts with other internal departments, as necessary, to plan and expedite project objectives | 09/16/2021 |
| 7963 | Gritstone Oncology Cambridge, MA RESEARCH ASSOCIATE, EPITOPE DISCOVERY (CONTRACT) B.S./B.A./M.S./M.A./PhD with a degree in cell biology, immunology, molecular biology or related field. Exp: 1+ years |
Gritstone bio is seeking a Research Associate to help discover novel T cell targets for multiple infectious disease and oncology programs. The primary role of the Scientist is to collaborate within and across teams to further develop and optimize a high-throughput epitope discovery platform to drive the therapeutic program and support key company initiatives. Approaches cover the broad spectrum of molecular/cell biology and immunology and include hands-on experience with flow cytometry and cell sorting, T cell cultures, nucleic acid extraction and PCR and DNA/RNA library construction. We are looking for an enthusiastic and adaptable team player who will thrive in a fast-paced dynamic and highly collaborative environment. This is an opportunity to work for a well-funded biotechnology company driving innovative infectious disease and oncology programs. | 09/16/2021 |
| 7964 | Ifyber Ithaca, NY Laboratory Technician BS degree. Exp: 1 year (more preferred) |
The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. | 09/16/2021 |
| 7965 | IGM Biosciences Mountain View, CA RA / Senior Research Associate, Pharmacodynamics and Biomarkers MS degree. Exp: 1+ years |
We are seeking a capable and driven Senior Research Associate with a background in Immunology or Immunology-Oncology to join our growing Pharmacodynamics and Biomarkers group. The candidate will play an integral role in the preclinical development of novel antibody-based therapeutics in a variety of disease areas and at various stages of development. The ideal candidate will have strong experience in standard cell-based in vitro immuno-assays, isolation and culture of primary cells, multi-dimensional flow cytometry, and common molecular techniques. Having experience with the phenotypic and functional characterization of clinical samples is a plus. The successful candidate must be able to work in a fast-paced, cross-functional, and highly collaborative team environment. | 09/16/2021 |
| 7966 | InBios International Seattle, WA Research Associate I A bachelor’s degree in a biologicals science. Exp: 1-2 years |
You have a biologicals, life sciences degree, academic or commercial lab experience with good simple buffer knowledge and experience and a firm scientific foundation, and you are eager to put your skills and knowledge to use in the commercial biotech assay research and development field. You also thrive in a fast-paced work environment where priorities and projects may change quickly. You are attentive and teachable and have a strong desire to learn new skills and you want hone those skills you have already begun to master under the supervision and instruction of the team’s lead scientist. You are a good teammate who is responsible and motivated and comfortable working closely in a team environment, where you openly share ideas and collaborate. You may or may not already have lateral flow immunoassay experience. (Prior experience with LFI is not required for the Research Associate I position.) | 09/16/2021 |
| 7967 | InBios International Seattle, WA Research Associate I/II - Cell Culture Bachelor’s degree in a microbiology, cell biology, molecular biology, or similar scientific discipline. Exp: 1-5 years |
We are seeking a motivated and diligent individual with strong aseptic skills and good experience in tissue culture, who has a keen eye for detail, and enjoys a busy workday under general supervision with daily goals working alongside a dedicated team that consistently meets deadlines and delivers products that meet high quality standards. | 09/16/2021 |
| 7968 | InBios International Seattle, WA Quality Assurance Associate I BS or BA in engineering or MS Exp: BS - 1+ years; MS -0+ years |
We are seeking a mindful and diligent individual with a warm and welcoming attitude who has excellent organizational and communication skills and a keen eye for detail. If you enjoy hands-on optimization and troubleshooting of equipment and processes, analytical work, leading and collaborating on projects, and being part of a reliable and dedicated Quality Assurance team, then we encourage you to apply for this position. | 09/16/2021 |
| 7969 | InBios International Seattle, WA Manufacturing Associate I - ELISA Bachelor’s degree with emphasis on life science. Exp: 1-year |
We would like to see your resume if you have received a degree with an emphasis on life sciences. If you have work experience in a GMP/ISO 13485 manufacturing facility and/or you have experience with PCR test-kit manufacturing please be sure to include that information on your resume or in a cover letter. If you would like to be part of a team responsible for the production of large-scale ELISA diagnostic test components in a BSL-2 laboratory, and you enjoy a busy workday under general supervision with daily goals working alongside a dedicated team that consistently meets deadlines and delivers products that meet high quality standards, then we encourage you to apply for this position. | 09/16/2021 |
| 7970 | InBios International Seattle, WA Manufacturing Associate I/II - Rapid Spray Bachelors degree in biochemistry, chemistry, or equivalent life sciences. Exp: 1 year |
We would like to see your resume if you have received a degree with an emphasis on life sciences. If you have work experience in a GMP/ISO 13485 manufacturing facility and/or you have experience with lateral flow test-kit manufacturing please be sure to include that information on your resume or in a cover letter. If you would like to be part of a team responsible for the production of large-scale later flow diagnostic test components in a BSL-2 laboratory, and you enjoy a busy workday under general supervision with daily goals working alongside a dedicated team that consistently meets deadlines and delivers products that meet high quality standards, then we encourage you to apply for this position. | 09/16/2021 |
| 7971 | InBios International Seattle, WA Quality Control Associate I (Short-Term/Full-Time) BS or MS in Bioengineering, Chemistry, Biology or other relevant discipline. Exp: 1 year |
You are looking for a short-term opportunity, which could possibly lead to a longer-term position dependent upon our business needs, working with a dedicated and reliable team of quality control professionals. You are a meticulous individual who thrives in an environment with demanding attention to detail; and you take pride in meeting deadlines, using your critical thinking skills, and working with your team and other teams to ensure top quality products are delivered. You have a warm and welcoming attitude and outlook as you approach each workday. If this describes you and the kind of team and work environment you are seeking, we encourage you to apply. | 09/16/2021 |
| 7972 | Instil Bio Thousand Oaks, CA Research Associate/Associate Scientist B.S/M.S in immunology, in molecular biology, bioengineering, or relevant degrees. Exp: 1+ year |
Instil Bio is seeking a highly motivated Research Associate/Associate Scientist to join the Process Sciences & Engineering group. The successful candidate will support the development of novel technologies and processes with the goal of creating cell therapies for the treatment of solid tumors. Responsibilities: - Perform multi-parameter flow cytometry assays. - Support process development studies to advance autologous T cell therapy products. - Authoring of study protocols, reports, procedures, batch records. - Presentation of experimental results to colleagues. - Provide hands-on support in a laboratory setting. - Other duties as assigned. | 09/16/2021 |
| 7973 | Instil Bio Tarzana, CA Quality Control Technician/Analyst - Molecular Biology BS in Cell and Molecular Biology or related Life Sciences Exp: 1+ years |
InstilBio is seeking a driven and enthusiastic Analyst in the Quality Control organization. The successful candidate will participate in lab start up activities, raw material inspection, routine in-process and final product testing by molecular biology and flow cytometry assays. As the site transitions into routine operations, the focus will be to help maintain the QC operations with related lab controls in compliance with regulatory requirements and commitments for clinical and commercial products. In this role, the QC Technician/Analyst will be expected to understand GMP principles, cell and molecular biology, raw materials process. | 09/16/2021 |
| 7974 | IntelliSyn R&D [X-Chem] Montreal, Canada, CA Associate Scientist (Montreal, Canada) MSc in Organic, Bioorganic or Medicinal Chemistry. Exp: 0 – 3 years |
IntelliSyn is seeking a candidate for the position of Associate Scientist. The Associate Scientist will work within a project team structure, design and execute synthetic routes and troubleshoot when needed. | 09/16/2021 |
| 7975 | Pace Analytical Naperville, IL Chemist Bachelor's degree in chemistry, chemical engineering, biochemistry required. Exp: 0-2 years |
The main function of a Chemist is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. The chemical technician will work in an experimental lab on research and development projects including hands on wet bench chemistry, chemicals handling, preparation of solutions/dilutions as well as routine analytical characterization and data analysis. Note: This position is expected to last 1 year. | 09/16/2021 |
| 7976 | Pace Analytical Naperville, IL Lab Tech - Wet Chem Bachelor’s degree in Chemistry, Environmental Science, Materials Science, or related field. Exp: 1+ years’ |
As a chemistry lab tech, you will assist in product research, development, testing, customer support, and corporate enhancement activities within the group. This role supports our client's RD&E division. Note: This position is expected to be 12 months in length. | 09/16/2021 |
| 7977 | Pace Analytical Dickinson, ND Lab Technician Bachelors Degree in Chemistry, Microbiology or science field. Exp: 1+year |
We are seeking a Lab Technician to execute analytical laboratory activities in support of chemical program monitoring and treatment recommendations. | 09/17/2021 |
| 7978 | Pace Analytical Maplewood, MN Lab Analyst - Microbiology BS degree in Biological science or related field. Exp: 1-3 years |
This position will actively support food safety and quality assurance through the use, and validation of, pathogen detection products. The analyst will prepare and evaluate samples using aseptic technique to ensure products meet specifications. The products being monitored are crucial to maintaining consumer safe food supply chains. Work is performed as part of a team in a collaborative environment. | 09/17/2021 |
| 7979 | Pace Analytical Woodbury, MN Electrochemist Bachelor's degree in Chemistry or related science. Exp: 1 year |
This candidate will be assisting in the set-up of a laboratory area and conducting long term electrochemical tests to assess the performance of new materials. | 09/17/2021 |
| 7980 | Pace Analytical Maplewood, MN Analytical Chemist – Stability Bachelor’s degree in Chemistry or related science field. Exp: 0-2 years |
This position will actively support the quality control testing of healthcare products through analytical testing. The products being monitored are crucial to patient’s safety efforts within the healthcare industry. Work is performed as part of a team in a fast-paced environment. | 09/17/2021 |
| 7981 | Pace Analytical Woodbury, MN Analytical Chemist Bachelor's degree in Chemistry or related science. Exp: 1-2 years |
Seeking an analytical chemist to perform QC analysis of inhalation device components using chromatographic instruments such as the GC. Note: Projected start date is mid- to late September 2021. | 09/17/2021 |
| 7982 | Dexcom San Diego, CA Process Development Engineer I B.S. in Mechanical Engineering, Bioengineering, or equivalent. Exp: 0-2 years |
In this role as a Process Development Engineer 1, you will use sound and proven engineering principles to assist in designing and developing processes and requirements. The projects and activities will focus on Dexcom’s future technology. Working as a member of a R&D process development team, you will collaborate with other engineers, management, and operators. This position will lead efforts to prove out manufacturing and automation processes to achieve design requirements, and explore and evaluate new technologies and concepts through analysis, prototyping, fixture design, and experimentation. This position will transfer and scale up new products from R&D. Involvement may begin from feasibility at vendors to full scale manufacturing. | 9/7/2021 |
| 7983 | Dexcom San Diego, CA Medical Device Engineer I - Materials Bachelor’s degree in a technical discipline. Exp: 0-2 years |
As a key member of the material science center within Dexcom’s research and development organization, the Material Engineer will work closely with other engineers, scientists, and technicians to support the development of next generation CGM sensor membrane material technologies. This is an exciting opportunity for an enthusiastic material engineer with a clear understanding of the technical and regulatory challenges of developing and validating materials used in medical devices. The individual will be responsible for assisting in the development, scaling, qualification, and operation of pilot-scale material processing unit operations and related analytical testing. The individual will also collaborate cross-functionally with operations, supply chain, quality assurance, vendors, and other stakeholders outside of the R&D organization. | 9/7/2021 |
| 7984 | Dexcom San Diego, CA Hardware Engineer I Bachelor’s degree in a technical discipline. Exp: 0-2 years |
Dexcom is expanding through a growing reputation as the technology leader in diabetes management and patient satisfaction. We have become the standard bearer in the emerging digital health space. We’re adding new staff who can further improve our innovative life-changing products. The position is for a Hardware Engineer 1 to develop our next generation Continuous Glucose Monitoring (CGM) embedded technology. You will understand low-power wireless technologies and glucose data generation and wireless data transfer between devices. As part of a team, you will design, implement and test embedded electrical systems for CGM. You will work to engineering project plans collaborating with internal R&D and Advanced Technology groups, along with our Quality, Operations, Regualtory and Clinical organizations. You will document your electrical solutions, following the relevant quality processes to meet Dexcom business needs. | 9/7/2021 |
| 7985 | Dexcom Mesa, AZ Microbiologist I Bachelor's degree. Exp: 0-2 years |
Coordinates microbiological testing, release of product and testing for validation protocols. Performs organism identification. Performs technical review of batch filling records to ensure quality of aseptic processes. Reads and interprets microbiological cultures and other related tests including but not limited to environmental monitoring, sterility tests, growth promotion, microbial limits tests and antimicrobial effectiveness tests. May perform validation, technology transfer and troubleshooting, and write policy procedure for quality initiatives. Reviews and approves environmental monitoring data and laboratory equipment and records. Prepares process and status reports, assigns and monitors document numbers and reviews documents for accuracy and completeness. Must have education and/or experience suitable for work in a biopharmaceutical or pharmaceutical manufacturing or similar environment. | 09/07/2021 |
| 7986 | Dexcom Dania Beach, FL Firmware Engineer I Bachelor’s degree in a technical discipline. Exp: 0-2 years |
Dexcom is expanding through a growing reputation as the technology leader in diabetes management and patient satisfaction. We have become the standard bearer in the emerging digital health space. We’re adding new staff who can further improve our innovative life-changing products. The position is for a Firmware Engineer to integrate our Continuous Glucose Monitoring (CGM) technology with other medical devices and information systems. You will learn low-power wireless technologies and understand glucose data generation and transfer between devices. You will design, implement, and test modular solutions. You will integrate Dexcom’s products with other partners’ technology. You will work to engineering project plans collaborating with internal Technical Services, R&D, Quality, and Operations organizations in addition to external partners such as Insulin Delivery Device Manufacturers, Academic Research Institutions, Contract Manufacturers and Compliance Labs. You will document your firmware solutions, following the relevant quality processes to meet Dexcom business needs. | 09/07/2021 |
| 7987 | Exact Sciences Redwood City, CA Biorepository Associate I Bachelor’s Degree in Biological Sciences. Exp: 1+ years |
The Biorepository Associate I is dedicated to collecting, banking, and processing human tissue and other samples for research and development (R&D) activities ranging from proof-of-concept experiments to clinical validation studies. The Biorepository Associate I will be responsible for the daily functions of the core as well as supporting growth into future areas of service. This position requires strong communication and organizational skills, and some degree of technical expertise including, but not limited to, knowledge of tissue handling, pathology and necropsy, biosafety protocols, and requirements of patient consent and privacy. | 09/07/2021 |
| 7988 | Exact Sciences Cambridge , MA Research Associate II Bachelor’s Degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical, Physical, or Biological Science. Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day-to-day experimentation, execution of bench experiments, and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in research and development projects assisting in the translation of research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 09/07/2021 |
| 7989 | Hovione East Windsor, NJ Process Engineer - Pharmaceutical Operations BSc / MSc in Chemical Engineering (or related field of Engineering or Science). Exp: 1-3 years |
The Process Engineer provides technical leadership of manufacturing projects at Hovione while ensuring optimal execution, customers’ satisfaction, product quality and project timelines and budget. This position will have a strong focus in particle engineering and drug product intermediates projects. The Process Engineer is also responsible for assuring that manufacturing operations are carried out in compliance with all Federal, State and Local requirements (namely EPA, OSHA, FDA and cGMP guidelines) and with Hovione internal policies and HSE requirements. | 09/07/2021 |
| 7990 | Eli Lilly Branchburg Township, NJ Research Assoc - QC Biochemistry B.S. or M.S. in Biological Science, Chemistry, or related field. Exp: BS 1-3 years; MS 0-1 years |
Perform routine duties of the maintenance of the Stability Program and the stability data base. Complete all stability-related tasks with coworkers and testing laboratories. Author stability studies and protocols to support routine manufacturing and investigations/change controls Monitor the stability pull schedule and ensure that samples are pulled and delivered to the laboratory on time. Proactively and effectively communicate with the QC testing laboratories and facilitate the timely completion of the stability samples. Communicate critical stability data and trends upward to QC management. Provide stability data necessary for the submission of various regulatory documents ensuring data accuracy and integrity. Monitor stability results and report any unexpected or adverse trends. Provide stability data to other departments upon request ensuring data accuracy and integrity. Author stability protocols with input from development groups and regulatory on design. Compile and write summary reports for the stability profile of the products. Contribute to the stability section of annual product reviews and regulatory filings. Write/revise SOPs. Conduct document reviews. Demonstrate initiative to assure performance of routine QC responsibilities. Apply good cGMP practices during execution of all work tasks. Assist coworkers in troubleshooting, laboratory investigations and problem resolution. Suggest process improvements to QC management. Work independently with supervisory guidance. | 09/07/2021 |
| 7991 | Meridian Medical Technologies [Pfizer] Andover, MA Associate Scientist, Analytical Research and Development (Bioassay and Impurity Testing) Bachelor’s degree in biology, biochemistry, immunology, biotechnology or related field. Exp: 1-2 years |
ROLE SUMMARY Bioassay and Impurity Testing Group: We are seeking candidates to join us in building capabilities to lead the industry in the advancement of novel products to the market through innovation and execution of analytical testing. Working within a team setting, the qualified candidate will be responsible for the development of analytical methods to monitor the intended mechanism of action of drug candidates and assays to evaluate process-related impurities in biological candidates in clinical development. The qualified candidate will have experience with PCR assays and/or immunoassays, which may be used for release testing and product characterization to ensure residual host impurities are controlled. This data is required to elucidate structure-function and to confirm suitable quality of clinical supplies in a broad biologic’s portfolio, including vaccines. The candidate will work across analytical functions and projects. Prior experience working in a GMP environment is desirable. Excellent writing skills and the ability to document and communicate results to a wide array of scientists and management will be critical. Ability to multitask while working with multiple people in a team-based environment is a requirement. | 09/08/2021 |
| 7992 | Meridian Medical Technologies [Pfizer] Pearl River, NY Associate Scientist (Cell-culture) BS/BA degree in life science (e.g. biology, cell biology, immunology, virology, microbiology). Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. Responsibilities will include: Order laboratory supplies such as plasticware consumables and reagents as needed for daily laboratory operation. Contribute and review documentation associated with protocols and SOPs, including data archiving, data review. Present experimental results at group meetings and project meetings. Write monthly progress report if applicable. Where applicable, performs job responsibilities in compliance with ccGXP regulations. Satisfactorily completes all training in conformance with departmental requirements. | 09/08/2021 |
| 7993 | Meridian Medical Technologies [Pfizer] Pearl River, NY Associate Scientist, Flow Cytometry Master's degree Exp: 1 years |
Incumbent will be responsible for testing samples for pre-clinical and early stage (Phase I) clinical studies as a member of the Clinical & Diagnostic Assay Development Group (CDAD). The candidate will also be responsible for maintenance and upkeep of multiple flow cytometers. The role is focused on flow cytometry assays but also includes performance of other cell-based assays on clinical samples. The role requires an in-depth technical knowledge of multi-parameter flow cytometry and good understanding of relevant software including FACS Diva and FlowJo. Experience of working in a BSL2 level tissue culture laboratory is required, as well as an understanding of cellular immunology and the key assay platforms of flow cytometry and ELISPOT. The role requires good analytical skills, attention to detail and the ability to clearly document and present complex biological data. Incumbent is required to multitask and work as part of a team that is required to meet business-critical deadlines. | 09/08/2021 |
| 7994 | Meridian Medical Technologies [Pfizer] Pearl River, NY Associate Scientist, Ligand Binding Immunoassays Bachelor’s or master’s degree in biology, microbiology, molecular biology, chemistry, or relevant field of science. This is a non-PhD position. Exp: 0-3 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to generate high-quality immunoassay data within the Ligand-Binding Immunoassay team in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs. You will perform Luminex assays to support toxicology and clinical studies across multiple programs. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs through responsibilities such as reagent preparation, equipment maintenance, inventory, assay troubleshooting/QC activities and data review. The incumbent uses Good Documentation Practices (GDP), follows established safety policies and procedures and performs all work in a compliant manner according to relevant Standard Operating Procedure (SOP) guidelines and cGLP guidelines. | 09/09/2021 |
| 7995 | Meridian Medical Technologies [Pfizer] Sanford, NC EM Analyst I BS/BA Degree in Science/related field with experience in biotech or pharmaceutical industry is preferred. Exp: 0 - 3 years |
Responsible for knowing, understanding and acting in accordance with Pfizer’s Values. Primary function of the job: These positions are specific to those able to perform environmental monitoring at the Sanford site. In addition, may be asked to perform tasks associated with maintaining GMP compliant Quality Control and Stability laboratories. Performs sampling including, but not limited to clinical and/or commercial environmental and utilities samples. Analyzes and interprets results, makes decisions regarding the accuracy, completeness and compliance. Responsible for reporting issues to management and participating in issue resolution (such as reporting variances and participating in associated manufacturing investigations, reporting hardware and software issues and assisting with troubleshooting, etc.) Assessing existing environments, processes and procedures and suggesting improvements to increase compliance and innovation. May initiate, develop plan and drive to completion continuous improvement project. | 09/09/2021 |
| 7996 | Precision for Medicine Houston, TX Technologist I - Laboratory Bachelor’s Degree (Life Sciences, Biology or other related discipline). Exp: 0-1 years |
Technologist I (Molecular) will need to have a broad skill set and good troubleshooting skills within the laboratory setting. Be able to work with scientists to develop and perform assays for molecular biology projects through assay development, validation, and execution phases in a timely manner. Perform assays according to SOPs and support development of new procedures and improvement of existing SOPs. Also, familiar and operating under CLIA. Responsible for training other staff. | 09/09/2021 |
| 7997 | Precision for Medicine Norton, MA Lab Assistant (Temp-to-Hire) 2p-to-10p - Laboratory Bachelor’s Degree (Biology, Chemistry, Life Sciences or other related discipline). Exp: 0-2 years |
The Lab Assistant will assist in shipment & receipt, the retrieval and preservation of biological samples that arrive daily or are stored in the repository. | 09/09/2021 |
| 7998 | Regeneron Tarrytown, NY Research Associate, Neuroscience (In vivo) Master's Degree Exp: one year |
We are seeking an associate to join our dynamic neuroscience research group. This person will perform hands-on research studies designed to investigate novel targets and mechanisms in neurodegenerative disorders. The primary focus of this will be Friedrich’s ataxia and motor neuron disease. As a Research Associate on the Neuroscience team, a typical day might include the following: •Designing and performing experiments to characterize in vitro and in vivo models of Friedreich’s Ataxia and screen potential therapeutic approaches in these models. •Conducting experiments in mice and rats, including handling, performing behavioral analysis, injecting compounds by a variety of routes, and dissecting tissues for histochemical and biochemical analysis. •Using a variety of cell lines including mouse ES cells, iPSC-derived neurons, and mouse primary neuronal cultures to screen therapeutics. •Isolating RNA from cells and mouse tissue and perform Real-time qPCR for quantification of gene changes from disease and therapeutic intervention. •Utilizing immunohistochemistry, biochemistry, and ELISA to profile in vitro and in vivo models of motor neuron disease and screen novel therapeutic compounds. •Performing data analysis on experimental data as well as troubleshooting under minimal direction. •Staying current on relevant literature in order to further develop scientific expertise, new assays and expand scientific/technical knowledge and skill sets. •Participating in group and departmental meetings and giving presentations. •Contributing to writing of protocols and articles for publication. | 09/09/2021 |
| 7999 | Regeneron Tarrytown, NY Research Associate, VI Next (In vivo) Master's Degree Exp: + 0 years |
VelocImmune (VI) Next is a technology development group at Regeneron that invents and develops state-of-the-art tools for biologic drug discovery. We are seeking a motivated, highly organized researcher to support our investigations of new antibody and cell-based therapies. This is an opportunity for a researcher with strong molecular biology & immunology skills to contribute to the development of industry-leading technologies and medicines. As the R&D Associate, VI Next, a typical day might include the following: Conducting and supporting experiments, independently and collaboratively, investigating new technologies in antibody and cell-based therapeutics. Constructing of DNA vectors, viral vectors, and cell-lines for in vitro and in vivo studies of candidate therapeutics. Maintaining, manipulating, and analyzing of mammalian cells lines and primary cells, using Crispr/Cas9, viral vectors, flow cytometry, cell transplantation, and immunologic assays. Immunizing mice with target antigen and analysis of B cell immune response, including activated B cell and plasma cell populations and antibody response by ELISA. Immunophenotyping and molecular analysis of new mouse models for drug discovery and disease investigation. Analyzing candidate therapeutics using in vivo mouse models of tumors, autoimmunity, and transplantation. Careful, thorough record keeping, data summarization, and presentation of results in formal and informal meetings. | 09/09/2021 |
| 8000 | Regeneron Tarrytown, NY Research Associate - IC Bioassay Development Bachelor's or Master's in a scientific field. Exp: BS 1-3 years; MS 0-1+ years |
Regeneron's bioassay group within the Therapeutic Proteins Department seeks a highly motivated and energetic Research Associate to join our highly collaborative team. In this role you will perform experiments for the in vitro selection and characterization of preclinical and clinical drug candidates in Regeneron’s pipeline. A Typical Day In The Role Might Look Like: Mammalian cell culture Generation of stable cell lines via plasmid- and virus-based techniques and CRISPR/Cas9 Cell-based reporter assays Flow cytometry for evaluating cell surface protein expression and antibody binding studies Isolation of PBMCs / primary leukocytic populations Primary cell functional assays evaluating, among others, cytokine release and effector function Plan experiments, including proper controls Analyze data accurately and in a timely manner Record data in an electronic notebook in an accurate and timely manner Communicate with supervisor and other lab members in an effective manner Present data within and outside the group clearly and concisely | 09/09/2021 |
| 8001 | Regeneron Tarrytown, NY R&D Associate BS/MS in a scientific field. Exp: 1-2+yrs |
Regeneron's Protein Development core, within our Therapeutic Protein area, which leads purification and biochemical characterization of protein reagents and antibodies in support of the company’s VelocImmune fully human antibody pipeline and Immune Oncology programs is looking for an R&D Associate. In this role, you will be primarily focused on purification of therapeutic reagents and antibodies for ongoing therapeutic programs using standard purification systems and some automated equipment. | 09/09/2021 |
| 8002 | Regeneron Tarrytown, NY R&D Associate (Metabolism and Liver Diseases) Master’s degree Exp: 1 year |
We are seeking a highly motivated and experienced research associate to join the Muscle and Metabolism Group to support our discovery and development efforts pertaining to lipid or liver metabolism. The individual will be responsible for the execution of in vitro and in vivo biological experiments necessary to develop cell-based and animal models for testing of experimental therapeutics and for mechanistic biology studies. The ideal candidate will have in-depth in vitro or in vivo technical expertise, be hardworking, flexible, innovative and able to function effectively in a fast-paced environment. They will also have excellent communication skills and be able to work well in a team. As an R&D Associate in Muscle and Metabolism, a typical day may include the following: · The candidate will also perform relevant data analysis and interpretation, collate data for presentation or reporting, and present data at group meetings · The candidate will be responsible for maintaining accurate and complete laboratory records. · In vivo technical expertise including, but not limited to: o Mouse handling, injections (IP, SC, IV) and bleeds · In vitro technical expertise including, but not limited to: o Tissue culture, transfections o Western blotting and ELISA o Basic molecular biology techniques This role may be for you if: · You have the ability to work well in a team · You possess excellent oral and written communication skills. · You have strong organizational and timely record-keeping skills. | 09/09/2021 |
| 8003 | Regeneron Tarrytown, NY R&D Associate, Quality Control Bachelors degree. Exp: 0-2 years |
We are looking for an R&D Associate to join the Quality Control team. Quality Control supports Bioanalytical Science, Protein Biochemistry and/or Analytical Chemistry at Regeneron. In this role, a typical day may include: Trains on, adheres to and builds knowledge of established procedures and protocols to perform a quality review of documentation. Reviews multiple documents within the same day. May multi-task across assignments. Routinely performs a high quality review. Learns to comfortably shift gears and priorities to meet changing needs, as required. Assembles all available resources to perform a quality review. Follows appropriate methods/protocols. Learns to evaluate the quality of documentation. Demonstrates foundational QC knowledge/skills in immediate area. Learns to follow appropriate approaches or techniques to resolve findings. Seeks direction and mentorship from others in decision making, as needed. Participates in sub-group and/or department meetings and may share results of work with others. Collaborates with and engages customers to improve documentation quality. Executes necessary operations in applicable software systems (e.g. LIMS, ELN, etc.) for a quality data review. May have ability to identify and troubleshoot routine challenges. | 09/09/2021 |
| 8004 | Fuji Film Cellular Dynamics Madison, WI Research Specialist - Process Engineering - (#370) Bachelor’s degree in chemical or bio-engineering, stem cell biology, cell biology, developmental biology, immunology or a closely related scientific f Exp: Up to one year |
We are recruiting for a Research Specialist - Process Engineering to support our continued growth and on-going development projects. Qualified individuals need have the capability, and to be inspired to support the development of therapeutics (cGMP) products and tools to support research endeavors. We aspire to improve the quality of life through our efforts. In return we provide development and support to enhance your career using cutting edge iPSC technology. In this hands-on laboratory role - you will focus on the scale-out, scale-up, optimization, and characterization of bio-processes for pluripotent stem cell expansion and directed differentiation of pluripotent cells to terminally differentiated cells. Design and execute experiments involving bioreactors, volume reduction technologies, and fill/finish operations. Write protocols and reports and contribute to the tech transfer of bio-processes to manufacturing. | 09/10/2021 |
| 8005 | Fuji Film Cellular Dynamics Madison, WI Research Specialist - Assay Development Group - (#368) Bachelor’s degree in biomedical engineering, stem cell biology, cell biology, developmental biology, immunology, or a closely related scientific fiel Exp: Up to one year |
FUJIFILM Cellular Dynamics, Inc in Madison, WI is recruiting for a Research Specialist to support our FCDI R&D Assay Development group. This position requires a self-motivated individual with experience in cellular and molecular biology who can contribute to our efforts to eventually expand assays across all FCDI platforms. Qualified individuals need to be inspired to support the development of not only assays for our therapeutics and discovery research products but help build structure to the newly formed FCDI Assay Development team. We provide development and support to enhance your career using cutting edge iPSC technology. In this role you will provide technical support for developing custom assays to evaluate the quality, purity and performance of FCDI iPSC-derived products. This position supports the development and optimization of cell-based assays using cell imaging and gene expression tools and instruments including, but not limited to flow cytometry, microscopy and PCR. | 09/10/2021 |
| 8006 | Steris Mentor, OH Associate Scientist I Bachelor degree in Biology, Microbiology, Molecular Biology, Biochemistry, or Chemistry is preferred. Exp: 0-5 years |
The Associate Scientist I manages multiple studies at different stages while performing efficacy testing in a clean room environment and detailed cosmetic evaluations of Medical Devices during Material Compatibility testing. | 09/10/2021 |
| 8007 | Steris Kalamazoo, MI Field Service Technician Associate’s or bachelor’s degree in electronics, mechanics or a similar discipline Exp: 1+ year(s) |
At STERIS, our Field Service Technicians act as the face of our company by ensuring top-notch service for our customers. In this field-based, customer-facing role, you will travel to medical and laboratory facilities to maintain, troubleshoot, service, and provide calibration and installation support for steam sterilizers, medical equipment washers and other STERIS products as needed. In addition, you will be responsible for building positive relationships with customers and colleagues, as well as completing necessary administrative tasks. Transferable skills for this role include mechanical (large military/agricultural equipment, appliances or vehicles), plumbing, HVAC, electrical, building maintenance and other similar field service repair work. | 09/10/2021 |
| 8008 | Steris Richmond, CA Technical Support Specialist - Software 2 yr Associate's or Bachelors degree in one of the related fields: Engineering, Audio/Video, Computer Science, MIS, CIS,Software Engineering, Techno Exp: 1 year |
The Technical Support Specialist- Software provides technical support to Customers, Partners and the Field Service Team to drive complete resolution of first responder and moderately complex issues, along with providing Part Identification assistance. Provides the first level support on field issues and implementation projects.Configures, installs, monitors, and supports multiple customer facilities that are using STERIS ORI hardware products,information management products including RealView, SAFE, ReadyTracker, Clarity, Video Conferencing, Streaming,etc. Provides direct phone support on STERIS ORI Hardware, enterprise software features and IT solutions.The Technical Support Specialist- Software is knowledgable in STERIS software solutions, hospital IT environments –including both LINUX and WINDOWS environments and ORI Products. They are also knowledgeable in , HIPAA,EMRs, HL7, PACS systems, and VNAs. The Specialist is expected to quickly address all incoming inquires deliveringtimely “service by phone” while delivering an overall extraordinary Customer experience. This includes investigating Customer questions about ORI Hardware, cybersecurity, IT environment setups, and ensuring the overall success of the software integration into their environment.They must manage the situation to de-escalate the situation while resolving the issue(s). The specialist leverages remote diagnostics, their experience with the products, understanding of the theory of their operation/safety hazards for the products and troubleshooting experience to resolve issues quickly. Inquires may include troubleshooting and corrective maintenance advice related to controls, electrical, IT/software, and electronics issues. They Configure, tests and deploys software applications and firmware changes delivered as Virtual Machines or on physical hardware. They will refer complex issues to Product Support Specialists and Senior Service Engineering staff. | 09/10/2021 |
| 8009 | Steris Brooklyn Park, MN Laboratory Technician III - $1,500 Sign-On Bonus!! Bachelor's Degree in Biology Exp: 1 year |
The Laboratory Technician III is responsible for executing and analyzing microbiological or chemistry testing in accordance with regulated laboratory testing techniques, approved procedures and Customer specifications. | 09/10/2021 |
| 8010 | Steris Spartanburg, SC Ethylene Oxide Analyst I - Spartanburg, SC Bachelor's Degree Exp: one (1) year |
Responsible for the activities related to EO operations including establishment of process parameters, program development, validations, cost reduction procedures, documentation and reporting as directed. Ensures effective communication with Customers, contract laboratories and AST associate | 09/10/2021 |
| 8011 | Steris Mentor, OH Software Engineer Bachelor degree in Electrical Engineering, Electronic Engineering, Computer Engineering, Systems Engineering, Software Engineering, Control Engineerin Exp: one year |
Are you looking for a place to put your innovative ideas to work? Bring your talent and experience to STERIS’ VHP team where you will design, develop, and execute software verification tests for medical devices following STERIS work instructions. You will maintain software project deliverables (cost, performance, time, quality) from inception to delivery, analyze product/system-level requirements, and translate them into software specifications, and maintain and develop the skills and knowledge of the software development team members. You will also help establish and improve the procedures, standards and tools. | 09/10/2021 |
| 8012 | UCB-group Boston, MA Research Associate - Protein Purification Bachelor’s degree in Biology, Biochemistry or Chemistry. Exp: one - two years |
To strengthen our Protein Purification team, based in our Boston office in Bedford MA, we are looking for a talented individual to fill the position of: Research Associate or Associate Scientist. As a Research Associate or Associate Scientist in the Protein Purification group, you will produce high-quality protein reagents to support UCB’s drug development pipeline. You will contribute by Purifying cytosolic, secreted, and periplasmic proteins utilizing the ATKA platform, SDS-PAGE and TFF. Characterizing and QC of purified proteins via HPLC and western blotting Troubleshooting challenging purifications, and participating in basic experimental design and protocol development Carrying out multiple complex experiments in parallel while maintaining rapid communication of experimental results with team members Documenting all data in company databases, and presenting results within and outside the Purification group | 09/10/2021 |
| 8013 | West Pharma Exton, PA Associate Scientist, Lab BS in Chemistry or related technical degree. Exp: 0-3 years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment. This role will be 2nd shift work. | 09/10/2021 |
| 8014 | West Pharma Kinston, NC Vision Engineer Bachelor’s degree in Engineering field. Exp: 1 - 3 years |
Support maintenance and enhancing current vision inspection systems in the manufacturing process to improve process control and finished goods quality. Troubleshooting mechanical and electrical systems on vision inspection systems. Contribute to upstream process improvements through use of Lean Sigma tools and understanding of rejected product root cause. Works as part of a global team and provide technical support to various functional teams. | 09/10/2021 |
| 8015 | Acrotech Biopharma [AUROBINDO] East Windsor, NJ MICROBIOLOGIST Master of Science Exp: Up to 3 years |
Microbiologist will perform a variety of Microbiology testing to assess the strength, identity and purity of test samples and/or materials. The Microbiologist will work as a member of team to effectively plan and Microbiology testing using established (official in USP and/or in-house) test procedures. The Microbiology may execute 90% - 100% of their work at the bench level. | 09/10/2021 |
| 8016 | Acrotech Biopharma [AUROBINDO] Durham, NC ASSOCIATE SCIENTIST MS in Science Exp: 0+ years |
In this role, you will be designing and independently conducting studies in support of metered dose inhaler (MDI) product development, with focus on formulation and process development. You will be routinely working with manufacturing equipment and testing apparatus / instruments. The candidate should have strong understandings of MDI formulation, components, and performance testing, with good knowledge of cGMP guidelines, FDA / ICH / USP guidances / monographs. Candidate also needs to have excellent problem solving and communication skills. Able to thrive in a team environment. | 09/10/2021 |
| 8017 | Acrotech Biopharma [AUROBINDO] Durham, NC ASSISTANT SCIENTIST BA/BS in Chemistry, Pharmaceutical Sciences or related field. Exp: 0+ years |
Capable of performing test methods for complex formulations under general oversight and documenting those experiments per cGMP requirements. Must be able to calculate, organize, and communicate results via standard data templates and reports. Experience in a cGMP laboratory and testing inhaled product (e.g. MDI and DPI) samples is preferred. Must possess good organizational skills, a commitment to quality work, and good oral and written communication skills, and work effectively as part of a team. | 09/10/2021 |
| 8018 | Cell Signaling Technology Beverly, MA Research Associate I Bachelor’s degree in a biological science (e.g. molecular biology, cell biology, biochemistry or biotechnology). Exp: 0-1 years |
The Research Associate I in the CST Antibody Production organization will perform centralized workflows as part of a core team in order to support the production, release, and maintenance of high-quality products and data. This position requires a balance between bench work, data management, and various cross-functional projects. | 09/10/2021 |
| 8019 | Jounce Therapeutics Cambridge , MA Research Associate / Senior Research Associate, Discovery B.S./M.S. in biology, biochemistry, immunology or related discipline. Exp: 1-2 years |
Jounce is looking for a Research Associate/Senior Research Associate Scientist specializing in In Vitro biology to join our Discovery Immuno-Oncology team. The successful candidate will be a highly motivated bench scientist committed to elucidating the mechanism of action, and enabling the development, of novel cancer immunotherapeutic biologics. They will generate data to support key decisions for project teams and actively participate in the interpretation of data and design of experiments. They will have the opportunity to work independently and collaboratively to advance portfolio programs in a dynamic and fast-paced environment. | 09/10/2021 |
| 8020 | Caribou Biosciences Emeryville, CA in vivo Pharmacology Research Assistant/Research Associate /Senior Research Associate Associate’s or Bachelor’s degree in life sciences or equivalent work experience. Exp: 1 year |
Caribou is seeking a Research Assistant/Research Associate/Senior Research Associate to join its in vivo Pharmacology team at its facility in Emeryville, CA. The candidate must be motivated, enthusiastic, professional, and committed to working as a team player. The ideal candidate combines confidence, comfort, and a working knowledge of laboratory animals, with a background in animal husbandry, restraint, and handling. In addition, experience with injection (IV, IP, SC, and PO) and blood draw techniques (RO bleed and cardiac puncture), is desirable but not required; experience with rodent surgery and anesthesia is a plus. On the job training is available. The candidate must have the ability to effectively communicate with coworkers and work as part of a team, follow instructions to work independently, and display a strong sense of ownership over their work. They must possess a strong attention to detail and always strive to perform quality work. This is an excellent opportunity to utilize and advance the ideal candidate’s laboratory animal skills in a state-of-the-art facility with a progressive, diverse, and knowledgeable team. | 09/10/2021 |
| 8021 | Catamaran Bio Cambridge , MA Research Associate/Sr Research Associate, Cell Process BS or MS in bioengineering, chemical engineering, biochemistry, chemical biology, biology, biophysics, pharmaceutical sciences, or equivalent/related Exp: 1-5 years |
Catamaran is seeking an experienced, hands-on Senior Research Associate / Research Associate to join the development team in assembling a state-of-the-art manufacturing process for our allogeneic NK cell drug product. The successful candidate will be responsible for optimizing our cell processes for NK cells, including cell isolation, engineering, expansion, harvest and cryopreservation. This role also includes technical process transfer to internal and external manufacturing sites in support of clinical trials of Catamaran programs. This will require authoring and reviewing technical reports and collaborating extensively with research and cell engineering teams. The ideal candidate has relevant experience in cell culture of primary human cells and cell-based assays, and is excited to join a small, fast-paced team with a “can-do” attitude to drive forward our new cell therapy platform. | 09/10/2021 |
| 8022 | Cel - Sci Elkridge, MD Raw Materials Associate B.S. Exp: 0-1 years’ |
The Raw Materials Associate participates in the routine release of materials required to aid in the manufacturing of Leukocyte Interleukin, Injection (LI) under current Good Manufacturing Practices (cGMP) for clinical application, and facilities operations and maintenance. Required to travel locally to an off-site manufacturing and contract facility. The Raw Materials Associate reports directly to the Manager of Quality Control. | 09/10/2021 |
| 8023 | Cel - Sci Elkridge, MD (with travel to North , MD Assistant Immunologist 4-year college degree in a relevant field. Exp: 0-2 years |
The Assistant/Associate Immunologist will assist in the day-to-day activities related to the QC testing of Leukocyte Interleukin, Injection (LI) under current Good Manufacturing Practices (cGMP) for clinical application, and QC equipment/facilities operations and maintenance. | 09/10/2021 |
| 8024 | Circle Pharma South San Francisco, CA Research Associate (Contract) B.S./B.A. in chemistry, biochemistry or related life scientific discipline. Exp: 1+ years |
We are looking to add a Temporary Research Associate to our growing Chemistry team. Reporting to our Chemistry Production Manager, our Research Associate will be responsible for the purification, synthesis and tracking of target molecules at Circle Pharma. Our ideal candidate will have experience in peptide purification with some experience with and exposure to solid phase peptide synthesis. Our ideal candidate will also have a proven track-record of productivity and project ownership, coupled with a solid understanding of organic synthetic concepts and analysis techniques. | 09/10/2021 |
| 8025 | ClearLight Biotechnologies Sunnyvale, CA Research Associate B.S. in immunology/molecular biology or related field. Exp: 1-3 years |
We are hiring research associates who will help develop the technology by analyzing customer tissue samples. This will involve clearing the tissue, immunostaining, imaging with 3D microscopes (confocal or lightsheet) and analysis of the 3D images. You will receive training in our specific technology but general familiarity with microbiology/histology analysis of tissue samples is expected. | 09/10/2021 |
| 8026 | Cogent Professionals [Scientific] Indianiapolis, IN Pharmaceutical Analytical Chemist MS - Chemistry Exp: 1-3 years |
Cogent Scientific, a life sciences workforce solutions company, is working in partnership with top tier companies in clinical, R&D and Drug Discovery arenas. We are able to offer you the chance to build on your skills and knowledge working among experts in their field and cutting-edge instrumentation. We aim to recruit the best people who stand out among their peers. Cogent Scientific offers an attractive benefits package and an exciting work environment. We currently have a role available for a Pharmaceutical Analytical Chemist. Job duties include, but are not limited to: Reverse phase purification (scale between milligrams to grams) using Agilent HPLC, LC/MS and NMR. Perform instrument maintenance/troubleshooting as needed. Working knowledge of ChemStation. Utilizing computers and software to research log files and program automated laboratory instrumentation. | 09/10/2021 |
| 8027 | Cogent Professionals [Scientific] Indianapolis, IN Pharmaceutical Chemist BS - Chemistry or related field. Exp: 1-3 years |
We currently have a role available for a Pharmaceutical Chemist. Job duties include, but are not limited to: Normal phase purification experience (scale between milligrams to grams). LC/MS experience. Basic ChemStation proficiency. Experience with Teledyne ISCO flash chromatography instruments (preferred but not required). | 09/10/2021 |
| 8028 | Concuir Consulting Orange County, CA ASSOCIATE CONSULTANT – ENGINEER I/II Bachelors or higher in Engineering or Science. Exp: 1+ years’ |
As a full-time employee of Concuir, Inc, you will provide consulting services to pharmaceutical, biotech and/or medical device clients. In this role, you will quickly learn client typical practices and be in a position to recommend and implement improvements to reach project goals. This is based on your experience as well as from Concuir’s portfolio of project management and cGxP best practices. Typical projects range from design through qualification of production equipment and/or utilities to modification or implementation of new facilities and process scale ups. | 09/10/2021 |
| 8029 | Cytek Biosciences Fremont, CA Reagent Manufacturing Technician I/II BS in Life Sciences or a related field preferred. Exp: 1-3-year |
Cytek Biosciences is a leading manufacturer and supplier of flow cytometry products and services. As a fast-growing company, Cytek aims to provide complete solutions for advanced cell analysis. We are seeking a motivated candidate who can assist in formulation, bottling and packaging of reagent products. The candidate shall be able to complete formulation and vialing activities per protocols or instructions. The candidate should have demonstrated attention to detail and have good communication, documentation and problem-solving skills. | 09/10/2021 |
| 8030 | Cytek Biosciences Fremont, CA Research Scientist I BS or MS degree in Life Sciences. Exp: 1-2-year |
Cytek Biosciences is a leading manufacturer and supplier of flow cytometry products and services. As a fast-growing company, Cytek aims to provide complete solutions for advanced cell analysis. We are seeking a motivated candidate who can assist in new reagent development, assay development and system verification. The candidate should be able to execute experiments independently following protocols or instructions. In addition, the candidate should have good communication, documentation, and problem-solving skills. | 09/10/2021 |
| 8031 | Cytek Biosciences Fremont, CA Reagent R&D Scientist I BS degree in Life Sciences. Exp: 1-3-year |
Cytek Biosciences is a leading manufacturer and supplier of flow cytometry products and services. As a fast-growing company, Cytek aims to provide complete solutions for advanced cell analysis. We are seeking a motivated candidate who can assist in new reagent R&D development and testing. The candidate shall be able to execute experiments and testing independently following protocols or instructions. In addition, the candidate should have good communication, documentation and problem-solving skills. | 09/10/2021 |
| 8032 | Ampac Analytical Rancho Cordova, CA Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Exp: One (1) to two (2) years |
We are looking for enthusiastic Chemists to join our QC Team in Rancho Cordova (Greater Sacramento area)! QC Chemist Duties (In-Process Group): Must use independent judgment to analyze and make determinations as to the quality of a product, using analytical equipment pertinent to the appropriate application of skills. Use various laboratory procedures related to analysis of bulk and pharmaceutical chemicals. Perform analysis of samples using various laboratory equipment and techniques such as FT-IR, Loss On Drying, Non-volatile Residue, Titrations, moisture analysis by Karl Fischer, in addition to other methods. Operate LC and GC systems in order to complete analyses of various types of samples. Maintain a thorough and neat laboratory notebook. Troubleshoot fixes for various instruments in the laboratory. May perform peer review of various commercial product laboratory data. The position uses critical thinking and understanding of highly specialized analytical equipment and chemical compatibility to accurately and safely analyze chemical entities in order to make a determination of the quality of manufactured pharmaceutical compounds. Equipment used: Analytical laboratory equipment. Use of chemical laboratory process and test equipment, specialized analytical equipment and various computer systems. Work place may include areas where a wide variety of chemical materials are used and stored. May involve potential exposure to variable noise levels. Must have a high consciousness for personal and equipment safety. The QC Laboratory runs 24/7/365, so candidates must be open to working all shifts. | 8/29/2021 |
| 8033 | Ampac Analytical Rancho Cordova, CA Analytical Scientist Bachelor's degree required or Master's degree in Chemistry preferred. Exp: One (1) to three (3) years |
We are looking for enthusiastic Scientists to join our Analytical Teams! We have opportunities at our Rancho Cordova, CA - (Greater Sacramento, CA) area location. We will pay to relocate you! Job Responsibilities: Candidate will develop and validate methods; provide analytical support to the research and development group to meet project goals; select appropriate methods and techniques in performing experiments; collaborate with analytical personnel to help develop routine analytical methods; work cross functionally to achieve target goals and proactively seek out potential solutions to issues. Candidate will also assist in creating method validation and/or qualification protocols and reports as well as analytical methods; perform all lab work that will support method validation, transfer, and qualification; perform qualification of primary and secondary reference material to be used as analytical standards. | 8/29/2021 |
| 8034 | Ampac Analytical Rancho Cordova, CA Analytical Scientist Bachelor's degree required or Master's degree in Chemistry preferred. Exp: One (1) to three (3) years |
We are looking for enthusiastic Scientists to join our Analytical Teams! We have opportunities at our Rancho Cordova, CA - (Greater Sacramento, CA) area location. We will pay to relocate you! Job Responsibilities: Candidate will develop and validate methods; provide analytical support to the research and development group to meet project goals; select appropriate methods and techniques in performing experiments; collaborate with analytical personnel to help develop routine analytical methods; work cross functionally to achieve target goals and proactively seek out potential solutions to issues. Candidate will also assist in creating method validation and/or qualification protocols and reports as well as analytical methods; perform all lab work that will support method validation, transfer, and qualification; perform qualification of primary and secondary reference material to be used as analytical standards. | 8/29/2021 |
| 8035 | Ampac Analytical Petersburg, VA Process Scientist Bachelor’s, Master’s or Ph.D. degree in Organic Chemistry required. Exp: Zero (0) to two (2) years |
AMPAC Fine Chemicals (AFC), an SK pharmteco company, is a custom manufacturer of active pharmaceutical ingredients (APIs, Drug Substances) and registered intermediates for customers in the pharmaceutical industry. Our integrated facilities located in California, Texas, and Virginia specialize in process development, scale-up, and cGMP compliant production from kilograms to multi-ton quantities. We are looking for enthusiastic Scientists to join our R&D Team! We have opportunities at our Petersburg, VA - Greater Richmond VA Area location. The Process Scientist position is responsible for production support and process development of pharmaceutical ingredients: Develops scalable manufacturing processes in an cGMP environment Conducts experiments to optimize processes for commercial manufacture Meets with groups internally and externally for project meetings and prepares data for presentations Effectively participates in Process R&D team meetings Works under supervision of more senior scientists or scientific directors to advance the company pipeline Thinks critically and creatively and is able to work independently and in interdisciplinary groups Ability to resolve problems and has strong organizational and planning skills * Demonstrates excellent writing and communication skills (both verbal and technical) and strong interpersonal skills. Education & Experience: BS, MS, PhD degree with some industry experience. Special Work Conditions: Work place may include areas where a wide variety of chemical materials are used and stored. May involve potential exposure to variable noise levels. Must customarily have a high consciousness for personnel and equipment safety. May be required to utilize a variety of personal protective equipment. May need to work outside of normal office hours. | 08/29/2021 |
| 8036 | Ampac Analytical Petersburg, VA Analytical Scientist Bachelor's degree required or Master's degree in Chemistry preferred. Exp: One (1) to three (3) years |
AMPAC Fine Chemicals (AFC), an SK pharmteco company, is a custom manufacturer of active pharmaceutical ingredients (APIs, Drug Substances) and registered intermediates for customers in the pharmaceutical industry. Our integrated facilities located in California, Texas, and Virginia specialize in process development, scale-up, and cGMP compliant production from kilograms to multi-ton quantities. We are looking for enthusiastic Scientists to join our Analytical Teams! We have opportunities at our Petersburg, VA - (Greater Richmond VA) area location. Job Responsibilities: Candidate will develop and validate methods; provide analytical support to the research and development group to meet project goals; select appropriate methods and techniques in performing experiments; collaborate with analytical personnel to help develop routine analytical methods; work cross functionally to achieve target goals and proactively seek out potential solutions to issues. Candidate will also assist in creating method validation and/or qualification protocols and reports as well as analytical methods; perform all lab work that will support method validation, transfer, and qualification; perform qualification of primary and secondary reference material to be used as analytical standards. | 08/29/2021 |
| 8037 | Angle plc Toronto, CA Manufacturing Associate I – ANGLE Biosciences Inc., Toronto Post-secondary education in life sciences or related discipline from an accredited college. Exp: 1-2 years |
This is an exciting time at ANGLE and at our Research and Development facilities in Toronto we are looking for a Manufacturing Associate I. As a Manufacturing Associate, you will work in a clean room and laboratory environment performing and documenting tasks and procedures according to our established Quality Management System SOPs and work instructions. In this role you will perform various tasks including receipt of incoming materials, processing materials, assembly and production of microarray devices and reagent kits, in-process and final test inspections and data entry. | 08/29/2021 |
| 8038 | BillionToOne West Menlo Park, CA Research Associate BS or MS in Molecular and Cell Biology, Microbiology, Biophysics, Biochemistry, or related field. Exp: 1-2 years |
Do you want to help develop prenatal and oncology diagnostics that can affect the lives of millions of patients? BillionToOne (ranked at the top 5% of Y Combinator companies) is currently seeking a research associate to join our interdisciplinary and innovative R&D team and help us develop novel molecular diagnostics. This person will be responsible for helping to design and performing the molecular assays and experiments under the supervision of our senior research team. This is a dynamic, start-up environment that requires adaptability and the ability to quickly learn and apply new concepts. | 08/29/2021 |
| 8039 | ArcherDX Boulder, CO NGS Laboratory Technologist (ADX-23-21) Bachelor’s degree in a science-related field required. Exp: Level I: 1 - 3 years |
Executes test methods to evaluate quality, functionality and stability of raw materials, in-process materials and finished products to ensure that they are in compliance with specifications for use in Good Manufacturing Practice (GMP) applications for In-Vitro Diagnostics (IVD). Tracks and identifies trends in QC data and recommends corrective actions when necessary. Assists in method transfer, method validation and method troubleshooting activities. Conducts out-of-specification (OOS)/out-of-trend (OOT) investigations as needed. Lead and support process improvement projects within all QC laboratories ensuring harmonization between the three labs. This position reports to the QC Supervisor, IVD. | 08/29/2021 |
| 8040 | Arcturus Therapeutics San Diego, CA Research Associate I/ II RNA Molecular Biologist/Biochemist Bachelor/Masters degree in molecular biology, biochemistry, or a related field. Exp: 1-2 years |
Arcturus Therapeutics is presently recruiting outstanding candidates with experience in the field of mRNA technologies and nanoparticle sciences. Our corporate culture is dynamic, diverse, and creative. We value collaboration and teamwork. We seek individuals to join us with a genuine passion for the science behind helping to cure disease and improve the lives of patients. | 08/29/2021 |
| 8041 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, Small Scale Oligo Synthesis B.S. Chemistry or Biochemistry degree with excellent understanding of organic and analytical chemistry. Exp: 0-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Chemist to join the Discovery Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, purification, analytical chemistry, and contributing to specific program goals. S/He will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 08/29/2021 |
| 8042 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, CMC Process Development BS/BA in Chemistry or related field. Exp: 1 year |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Chemist to work as a Chemist in the Chemistry, Manufacturing, and Controls Group focusing on small molecule process development. This is an ideal position for an individual with an organic chemistry background who has an interest in projects related to novel technology in synthesis and purification of small molecules and bioconjugates. | 08/29/2021 |
| 8043 | Astellas Seattle , WA Research Associate I, Core Technologies in Seattle, Washington BS Degree. Exp: 0-3 years |
The primary purpose of a Research Associate I for our Core Technologies Department is to contribute to the further molecular engineering for our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to culture pluripotent stem cells as well as run molecular and cellular assays to characterize our proprietary Universal Donor Cells. | 08/29/2021 |
| 8044 | Aurora Biolabs San Diego, CA Research Associate I Bachelor's Degree in science related field. Exp: 0-1 year |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 08/30/2021 |
| 8045 | Avid Bioservices Tustin, CA Research Associate/Sr. Research Associate, Downstream (Purification) Process Development Master's Degree Exp: 1 to 2 years |
The Research Associate provides laboratory support for Process Development and performs a range of activities (while the Sr. position performs at a senior level). The employee may be assigned various tasks within the department to complete. | 08/30/2021 |
| 8046 | Axial Therapeutics Woburn, MA Research Associate, Biology Bachelor’s degree in biology, biochemistry or a related field preferred. Exp: 1-3 years |
In this role the Research Associate will support biology as a member of a highly matrixed drug discovery team and will be responsible for the execution and troubleshooting of various biological assays and experiments. This pro-active researcher will collaborate with team members, identify opportunities to improve efficiency, share ideas and expertise and contribute to Axial’s creative, dynamic and collaborative culture. | 08/30/2021 |
| 8047 | Axis Clinicals USA Dilworth, MN Analytical Chemist I Bachelor’s degree in Biology, Chemistry, or equivalent. Exp: 1 year |
The Analytical Chemist I, Bioanalytical Operations carries out various Bioanalytical functions of the organization. The Analytical Chemist is responsible for executing Bioanalytical methods within AXIS Clinicals. | 08/30/2021 |
| 8048 | Berkshire Sterile Manufacturing Lee, MA Process Engineering Associate BS/MS in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science Exp: 6 mo. or more |
As a BSM Process Engineer you will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 08/30/2021 |
| 8049 | Biocare Medical Pacheco, CA Acssociate I, Protein Chemistry Bachelor’s degree in a scientific field. Exp: one plus (1+) years’ |
The Protein Chemistry Associate I will take an active role in material processing, reagent formulation, technical manufacturing, and in-process and/or final quality control of reagents for use as components of in-vitro diagnostic (IVD) products. Specifically, he/she is involved in bioconjugation, protein purification, and analytical characterization of complex bioconjugates as they relate to the development of tissue diagnostic products for cancer and infectious disease. This position requires the person to adhere to all current industry standard regulations. | 08/30/2021 |
| 8050 | Biotium Fremont, CA RESEARCH ASSOCIATE, MOLECULAR BIOLOGY B.S./M.S. in Molecular Biology, Biochemistry or a related field. Exp: +1 years |
This role will be responsible for performing production-scale nucleic acid purifications and nucleic acid detection using fluorescence assays and quantitative PCR. The successful candidate will have experience handling DNA and RNA, and be capable of demonstrating careful pipetting technique in sensitive assays. This individual will play an important supporting role in the design, optimization, and assessment of new nucleic acid detection products. | 08/31/2021 |
| 8051 | Visby Medical San Jose, CA Lab Technician (Contractor) Bachelor's degree in a scientific field preferred. Exp: 1-2 years |
The Contract Laboratory Technician will be responsible for providing laboratory support for research and product development. The Technician will perform a variety of duties in support of research goals, objectives, and protocols. | 08/31/2021 |
| 8052 | Visby Medical San Jose, CA QC Analyst I - Temp Bachelor’s degree, preferably in a scientific field. Exp: 0-2 years |
The QC Analyst I a temporary role is an enthusiastic individual with great communication skills and will be a part of a high performing team. This role is responsible for performing various test methods to evaluate the quality of raw materials, manufactured materials, and finished goods. | 08/31/2021 |
| 8053 | Visby Medical San Jose, CA QC Technician - Temp Bachelor's degree in scientific field preferred. Exp: 0-2 years |
The QC Technician temp role is responsible for quality control testing of raw, intermediate, and finished goods in support of Incoming Inspection and the Manufacturing processes. The QC technician will perform a variety of duties in support of Quality Control department goals and objectives. | 08/31/2021 |
| 8054 | Boston Institute of Biotechnology Southborough, MA Research Associate / Scientist / Sr. Scientist – Downstream Process Development MS degree in Biochemistry or Chemical Engineering. Exp: 0-5 years |
Essential requirements for this position include in-depth understanding and hands-on experience with recombinant protein purification from different expression hosts (including E. coli, Yeast, CHO and HEK) and an aptitude for careful, detail-oriented experimentation. The level of the position will be commensurate with the candidate’s experiences. | 08/31/2021 |
| 8055 | Cabaletta Bio Philadelphia, PA Associate Scientist / Scientist, Molecular Biology MS degree Exp: 1 - 2 years |
Reporting to the Senior Director Gene Transfer Technologies, the Associate Scientist/Scientist, Molecular Biology will perform tasks aimed at generating genetic constructs to be used for advanced manufacturing of next generation cell therapies. The ideal candidate will be well versed in most current cloning technologies and perform multi-step procedures under limited technical supervision. Prior exposure to molecular cloning procedures related to gene editing and transposon-mediated gene transfer is beneficial. The position offers growth potential due to the rapid increase in new gene transfer technologies and the addition of new pipeline products. | 08/31/2021 |
| 8056 | Bayer Waltham, MA Associate Scientist, Purification Master’s degree Exp: 0-3 year |
Abcam is looking for a Scientist to join our team in Waltham, MA, working to purify and analyze high quality recombinant proteins for development as standalone products at Abcam. The goal of this product line is to deliver outstanding products to our customers and help Abcam achieve our aim of being the most influential company in life sciences by helping advance global understanding of biology and causes of disease, which, in turn, will drive new treatments and improved health. | 09/01/2021 |
| 8057 | Abiomed Danvers, MA Product Development Engineer I BS in Mechanical, Biomedical Engineering or directly related scientific discipline. Exp: 1 year |
We are a dynamic development team that drives innovative solutions to improve patient care. As a Product Development Engineer you will support and own technical efforts, design initiatives, and engineering activities for next generation Impella systems. You’ll have a tangible impact on our business and be rewarded by a positive impact to patients' lives. | 09/01/2021 |
| 8058 | Agilent Carpinteria, CA Bio-Chemical-Manufacturing Associate, Production #RM4008843 Bachelors or Master's degree in Biological Science or a closely related field or equivalent (Science course-work related to biochemistry, molecular bi Exp: up to 2 years |
The Manufacturing Associate will be responsible for formulating reagents related to Biochemical operations, and to ensure consistent quality compliance with Agilent policy. Following approved formulas/recipes, you will ensure established standards for safety, quality, quantity, service and cost standards are maintained. Ensure results are delivered against specific goals by effectively planning and organizing. Develop and manage processes and systems to meet the current and future business needs. As a Manufacturing Associate, you will manufacture products to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. Your proficiency in analytical testing, molecular pathology and immunohistochemistry applications will be required to perform in-process quality control on a variety of products. You will have an opportunity to become skilled in the use of a wide range of lab instruments, including but not limited to spectrophotometers, conductivity meters and auto-pipettors, all of which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are critical. Continuous Improvement is a priority in our organization. | 09/01/2021 |
| 8059 | Agilent Atlanta, GA Bio Molecular Field Service Engineer #RM4007324 A Bachelors or master’s degree within the science field – e.g. chemistry, analytical chemistry biochemistry, biotechnology or similar. Exp: 0-2 years |
Every day, Agilent Field Service Engineers help our customers to solve issues that enable scientists to make discoveries that enhance the quality of life. Through our work, we deliver insights and provide support that keep labs running smoothly and more efficiently. Join our dynamic organization to be a part of this rewarding work. As a Field Service Engineer for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software and consumables is key. Applying your interpersonal skills, creativity and can-do attitude is essential. The ability to help with solving customer problems and a dedication to deliver the highest-levels of customer service is how you will build customer success. | 09/01/2021 |
| 8060 | Agilent Carpinteria, CA Laboratory Assistant #RM4005496 Bachelors in biological sciences preferred. Exp: a year |
This laboratory assistant position will have duties both in the lab and at the desk. The position will support the tissue procurement department that will include tasks and documentation to move new donor samples through incoming quality control to delivery of qualified samples to internal teams. It will involve histology instrument operation and maintenance, working with donor tissues and slides, engaging with R&D staff, general lab maintenance, documentation and review, sample labeling, data reconfiguration and scanning. In addition, this position requires daily coordination and collaboration amongst our team, which includes, but is not limited to, brief daily meetings and one extensive team weekly meeting. Good interpersonal skills and flexibility in shifting prioritization of tasks is required. Basic laboratory tasks such as cleaning, equipment documentation and reagent preparation will be included. | 09/01/2021 |
| 8061 | Agilent Carpinteria, CA Research Associate Entry #RM4006317 4-year university degree in biological or chemical sciences. Exp: Entry |
Works on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. | 09/01/2021 |
| 8062 | AstraZenica South San Francisco, CA Associate Scientist, Biology Bachelor’s degree in biochemistry, molecular biology or related discipline required. Exp: 1 year |
The Associate Scientist, Biologysupports the Biology Department’s aims in translational science, clinical trial support, and pre-clinical drug development. This position involves hands-on execution of experiments, processing primary patient samples, maintaining equipment, preparing reagents, inventory management and other routine lab maintenance. | 09/01/2021 |
| 8063 | AstraZenica Gaithersburg, MD R&D Associate I/II - Cell Therapy (CAR-T) - BPD BS/MS in Chemical/Biochemical Engineering, Biotechnology, Biochemistry, Cell Biology, Immunology or Biological Sciences. Exp: RA I - 0+ years |
Main Duties & Responsibilities: Design and execute lab experiments to support CAR-T process development; Record, interpret and report experiment data in a clear and concise manner and communicate results to team members; Present experimental results at internal and external meetings; author and contribute to scientific publications, patents, and regulatory submissions; Work effectively and collaboratively as a team member within a highly matrixed organizational structure; | 09/01/2021 |
| 8064 | AstraZenica Gaithersburg, MD Associate Scientist – Cell Therapy Formulation Development Degree in Chemistry, Biochemistry, Pharmaceutics, Chemical/Biochemical Engineering or related field (Bachelor’s Degree). Exp: 0+ years’ |
Main Duties & Responsibilities: Support early stage formulation development activities for the development of cell therapy, oncolytic viruses, Adeno-Associated Viruses, monoclonal antibodies, and novel biotherapeutics. Perform analytical assays in support of solubility, stability and elucidation of degradation mechanisms. Design, develop and execute experiments in the areas of pre-formulation, formulation screening and development, cryopreservation, lyophilization, fill-finish, and/or biophysical characterization. Provide detailed observations, analyze data, interpret results, maintain documentation, and prepare precise technical reports, summaries and protocols with minimal supervision. Present findings at internal meetings and/or contribute to the preparation of manuscripts and patent applications. Function effectively as a member of one or more project teams. | 09/02/2021 |
| 8065 | AstraZenica Redwood City, CA QC Analyst- Redwood City, CA Bachelor of science degree, preferably in chemistry or microbiology. Exp: 0-5 years |
Provide technical and analytical support to the Quality Control (QC) function through routine and non-routine analytical testing, instrument operation and troubleshooting, and data analysis. The individual will focus on performing analytical testing, data review, and leading projects at the QC department level. The individual should be qualified to an undergraduate level/or equivalent in a scientific field. Must have knowledge and understanding of analytical chemistry and laboratory instrumentation. Must have understanding of the QC function, and its role and importance to the business.: Perform laboratory activities according to local test methods and standard operating procedures (SOPs) Operate laboratory instruments for physical characterization tests (e.g. particle size analyzer, Karl Fischer oven titrator) Operate chromatographic instruments and software (e.g. GC, HPLC, Empower) Detail all testing activities within an electronic laboratory notebook with emphasis on ALCOA principles (attributable, legible, contemporaneous, original, accurate) Utilize software to perform analytical testing, data entry, data analysis (e.g. electronic lab notebook, LIMS, SAP) Supervise laboratory instrument performance and perform troubleshooting as needed Author protocols, validation reports, risk assessments, trend reports, and technical justifications Support and lead problem-solving activities for deviations and laboratory investigations Support and lead change controls and continuous improvement initiatives | 09/02/2021 |
| 8066 | Bachem Torrance, CA Analytical Scientist, Method Development & Validation Master’s Degree in analytical chemistry or related scientific field Exp: 1 year |
The Analytical Scientist will fulfill a critical role in GMP operations. This individual helps with the execution of feasibility evaluation of analytical methods, method development and validations, writing of validation protocols, reports and other technical quality documents; conducts validation related investigations and contributes to improvements in laboratory operations. | 09/02/2021 |
| 8067 | Biomarin Pharmaceutical San Rafael, CA RESEARCH ASSISTANT / RESEARCH ASSOCIATE, CELL AND MOLECULAR BIOLOGY ASSAY DEVELOPMENT, BIOLOGY RESEARCH Bachelor’s degree in scientific discipline Exp: 0-2+ years |
We are searching for a highly motivated Research Assistant/Research Associate (I/II)to join the Biology Research department within BioMarin Research and Development. The candidate will be responsible for implementing and performing biochemical, molecular, and cellular assaysin support ofthe BioMarin research pipeline. This position offers a unique career opportunity to work in a matrix-based team environment on multidisciplinary aspects of drug development. The successful candidate will interact with other members of the Biology Research department as well as collaborators to support our therapeutic discovery programs. Applicants should have an MS or BS in a relevant field with hands on laboratory experience. Ability to work collaboratively on project teams, being resourceful, taking initiative, and attention to detail are essential. Candidates should be scientifically flexible in working in a variety of disease areas as business needs change and be good at learning and mastering new skills. | 09/02/2021 |
| 8068 | Biomarin Pharmaceutical Novato, CA RESEARCH ASSOCIATE Master's degree in Biological Sciences Exp: 1 year |
The Analytical Sciences department at BioMarin Pharmaceutical Inc. is seeking a skilled Analytical Biochemist and/orBiologist at the Research Associate level to join a team focused on supporting gene therapy & enzyme replacement therapy. The successful candidate will be a self-motivated, independent and critical thinker who has experience to work in a multi-disciplinary and fast-paced environment, and solid communication skills. The candidate will developand execute a wide variety of analytical methods and assays for the characterization of therapeutic candidates in developmentwith a particular focus on critical program needs including CMC development for INDs and BLAs. An ideal candidate will have experience in cell-based assays. | 09/02/2021 |
| 8069 | Biomarin Pharmaceutical Novato, CA RESEARCH ASSISTANT Bachelors degree in biological sciences or related discipline. Exp: 0-2 years |
Primary responsibility is to support the Assay Services subgroup within Analytical Sciences. This position involves performance of a variety of analytical assays with adherence to strict timelines. Assays may include enzyme activity, total protein, cell-based bioassays, chromatography and electrophoresis, done under the supervision of more senior personnel. Assists in the qualification of assay methods and in their transfer to the Quality Control laboratories. Provides major contributions to the evaluation of drug substance and drug product. Receives and records results for Assay Services in support of a variety of different groups including QC, MFG, Cell Culture PD, Purification PD and Formulation. Responsible for operational aspects of the laboratory through ordering, equipment maintenance and organization. This position will also record and interpret data generated and properly record into the company Electronic Notebook and/or Labware LIMS. | 09/02/2021 |
| 8070 | Biomarin Pharmaceutical Novato, CA RESEARCH ASSOCIATE 1 Master’s Degree in Biology or a related scientific field. Exp: 0-2 years’ |
Team member will support process development and technical transfer of upstream production through various stages of development to manufacturing. This position will include working with new technologies such as gene therapy as well as protein therapeutics.The individual will need to demonstrate technical proficiency enabling effective execution of experiments and basic problem solving; strong verbal and written communication skills; ability to work effectively in groups.The position will focus on small-scale cell culture activities, developing processes in bench-top bioreactors, as well as scale-up activities that may involve the transfer of processes to commercial facilities. The preferred candidate has experience in upstream bioprocessing,withfamiliarity in bioreactor and harvest centrifugation/filtration operations.Experience with insect cell cultures, viral vectors or gene therapy is also preferred. Furthermore, the candidate would be expected to analyze culture samples via various analyticaltechniques. The individual will develop competence in analysis and interpretation of data. The candidate will organize results using electronic lab notebook and other digital data archive systems. | 09/02/2021 |
| 8071 | Bristol Myers Squibb Summit, NJ Research Associate, Viral Vector Process Development M.S. or B.S. in Biochemistry, Molecular Biology, Bioengineering, Chemical Engineering, or related disciplines. Exp: 0-2 years |
The Research Associate will be a member of the viral vector process development (VVPD) group supporting clinical and commercial cellular products. This Research Associate will start with approximately 6 months of training with the current viral vector process development group in Seattle, WA before permanently residing in New Jersey. The training in Seattle will ensure the Research Associate will have hands-on training with the various processes for lentiviral vector and adeno-associated viral vector production. Upon relocating to New Jersey, the Research Associate will be part of the team that will establish the joint viral vector lab which will be shared between viral vector process development and vector manufacturing sciences and technology (MSAT). The primary focus of this research associate is to perform lab work to establish scale down models, support closure of manufacturing deviations, implementation of new technologies into vector manufacturing. | 09/02/2021 |
| 8072 | Bristol Myers Squibb Devens, MA Associate, QC Microbiologist Environmental and Facilities Monitoring B.S., in biological sciences, a related discipline. Exp: 0 - 2 years’ |
Bristol-Myers Squibb has a great entry-level role at our Devens, MA open now! We have a need for a QC Microbiologist Environmental and Facilities Monitoring Associate! As our Associate, you will perform environmental monitoring's and routine testing. | 09/02/2021 |
| 8073 | Bristol Myers Squibb Bothell, WA Associate I, Quality Control Microbiology, Cell Therapy BS in Scientific discipline. Exp: 0-3 years |
The primary focus of the Quality Control Associate I role will be to support drug product lot release and in-process testing within a cGMP environment. This position reports to the manufacturing site Sunday to Wednesday 0600-1630 (6AM-4:30PM) Perform environmental monitoring sample collection, sample receipt, sample incubation, and downstream results analysis, interpretation, and reporting. Perform or support cGMP lot release, in-process, and stability testing using various test methods and procedures. Ensure timely completion of testing and tasks as assigned. Support assay transfer and method validation of by executing cross-site validation protocols and providing data to support final reports. Identify opportunities for continuous improvements. Maintain instrumentation and equipment preventative maintenance and supporting documentation in a cGMP compliant manner. Assist in the implementation of new assay methodologies and the associated instrumentation. Identify and support initiation of Deviations, CAPAs and Laboratory Investigations. | 09/03/2021 |
| 8074 | Bristol Myers Squibb Seattle , WA Research Associate, Critical Reagent Management BS in a scientific discipline. Exp: 1-3 years |
In this individual contributor, lab-based role, the Research Associate will work in a collaborative environment to generate quality reagents in house and manage the critical reagent inventory to support routine testing in Analytical Operation and Clinical QC. This position will report to the Manager of the critical reagent management team in Analytical Operation. | 09/03/2021 |
| 8075 | Bristol Myers Squibb Seattle , WA Research Associate, Gene Editing in Cell Therapy Bachelor’s or Master’s degree in biology, molecular biology, microbiology, cell biology, or similar scientific discipline. Exp: 1 year |
We are looking for a highly motivated, dynamic and self-driven individual to join the Immuno-Oncology & Cellular Therapy Gene Editing team in Seattle. Reporting to a Sr. Associate Scientist in the Immuno-Oncology & Cellular Therapy group in Seattle, the primary focus of the Research Associate role will be to advance our non-viral delivery technology for gene editing applications. The associate will be responsible for generating and gene editing CAR-T cells, assessing editing efficiency, and be in the lab full time helping to push gene editing projects forward. The key deliverables for this role are: 1) set up assays to evaluate gene editing both functionally and molecularly 2) show competency in stimulating, culture, transduction, and transfecting primary T cells 3) help develop novel tools and protocols for a clinical gene editing application. | 09/03/2021 |
| 8076 | Bristol Myers Squibb Seattle , WA Research Associate, Raw Material Testing B.S. in Chemical/Biological Engineering, Immunology, Biology or relevant scientific discipline. Exp: 0-2 years |
The Raw Material Testing group is seeking an enthusiastic Research Associate to act on development and execution of critical raw material testing protocols in support of engineered T-cell programs, commercial and clinical manufacturing. This role will require to deliver high quality work and timely output in a cellular therapeutic manufacturing environment. | 09/03/2021 |
| 8077 | Bristol Myers Squibb Seattle , WA Research Associate, Gene Editing Raw Materials Process Development M.S. or B.S. in Biochemistry, Molecular Biology, Bioengineering, Chemical Engineering, or related disciplines. Exp: 0-2 years |
We are seeking an enthusiastic, self-driven individual to join the Viral Vector & Gene Editing Process Development team. Our team develops process and technology underpinning critical raw materials used in the manufacturing of engineered T cells, including gene editing raw materials. The primary focus of this research associate is to support process development, production and characterization of gene editing raw materials which are critical inputs to our CAR-T drug products. The candidate will support current programs and advance our understanding in gene editing raw materials. | 09/03/2021 |
| 8078 | Brooks Life Sciences [GENEWIZ] South Plainfield, NJ Associate Scientist - Evening Shift Bachelor’s Degree in Biological Sciences required. Exp: 1+ years |
The Associate Scientist position in our Next Generation Sequencing department is a great entry-level role with room for growth and advancement. If you have the desire to work in a casual yet results-driven environment that embraces innovation- then you’re just what we’re looking for! | 09/03/2021 |
| 8079 | Covance [Labcorp Drug Development] Indianapolis, IN Research Assistant -Immunochemistry Bachelor of Science/Arts (BS/BA) degree in related scientific field. Exp: 1- 2 years |
Analyzes biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. | 09/03/2021 |
| 8080 | Covance [Labcorp Drug Development] Chantilly, VA Lab Analyst-BioA Bachelor of Science/Arts (BS/BA) degree in Biology or related scientific field. Exp: 1 year |
Analyzes biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. | 09/03/2021 |
| 8081 | Covance [Labcorp Drug Development] Greenfield, IN Study Technician (Research Assistant) Pathology - $18/hr! Bachelor’s Degree in Life Sciences, or Associate Degree in Histology, Laboratory Animals Technology or Veterinary Technology. Exp: No professional experience required. |
Do you have dissection experience? Are you interested in Histology? Necropsy? Pathology? Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. We are offering a sign-on bonus of $3,000 ($1,500 upon hire and $1,500 after 6 months). What you will be doing As a Research Assistant (Study Technician) you’ll apply your scientific curiosity in Biology, Physiology, Neuroscience, Animal Science, Zoology, Biochemistry, Genetics, Microbiology, Immunology or similar majors researching the effectiveness, safety and toxicity of drugs in early development animal research studies. At our Greenfield, IN lab, you will be performing basic necropsy or histology tasks on a variety of laboratory animals in compliance with the appropriate Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs) and regulatory guidelines: Perform basic duties of necropsy and/ or basic duties of histology. Trim wet tissues. Embed tissues into paraffin. Tissue staining techniques. Microtomy. Report all animal care concerns and become involved in the resolution and appropriate corrective action, when necessary. How you will be rewarded Working in Greenfield, IN our Pathology Research Assistants: Earn a starting hourly rate of $18.00. Work primarily 1st shift, with some overtime. Enjoy 24 days of personal-time-off (PTO) (pro-rated depending on start date) Have access to other great benefits including: tuition reimbursement, paid holidays, a 401(k) plan with a generous company match and of course medical and dental insurance. You'll have access to growth opportunities With the support of exceptional people from across the globe, you’ll be empowered to own your career journey with: Formal and informal mentoring opportunities. Extensive training and job shadowing opportunities. Personalized development planning. Exposure to many drug development scientific career paths. | 09/03/2021 |
| 8082 | Invivotek Hamilton , NJ Research Associate (in-vivo) Bachelor of Science degree in Life Sciences. Exp: 1 to 2 years |
We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 8/14/2021 |
| 8083 | Invivotek Hamilton, NJ Research Associate B.A. or M.S. in biochemistry, molecular biology or related field. Exp: 1 year |
The Oncoveda Cancer Research Center of Genesis Biotechnology Group is looking for a motivated individual to work as a Research Associate. The successful candidate will contribute to the work of a multi-disciplinary community of scientists, supporting the development of novel therapeutics. This position is one site everyday in our Hamilton, NJ location. | 8/14/2021 |
| 8084 | Immucor Atlanta, GA Biological Quality Assurance Technician Bachelor’s degree in Microbiology, Biology, Medical Laboratory Science. Exp: 1-2 years’ |
We are looking for a Biological Quality Assurance (BQA) Technician to join our QA team. The Biological Quality Assurance Technician is responsible for the microbiological testing and environmental monitoring to confirm the quality of products at Immucor, Inc. As the Biological Quality Assurance Technician, you will be principally responsible for collecting samples for environmental monitoring, including but not limited to air, water, surface and personnel. | 8/16/2021 |
| 8085 | Immucor Virtual , US Technical Support Representative III - Transplant in United States Master’s degree. Exp: 1 or more years |
We are seeking a Technical Support Representative III to be a part of our growing company. As a Product Support Representative, you will provide domestic and international customer support and troubleshooting of Lifecodes products, both over the phone and on site. We offer competitive salaries and benefits, as well as opportunities for professional advancement. This is a challenging and rewarding opportunity for a highly skilled candidate.If you’ve got the necessary skills and experience to excel in this position, we want to hear from you. Apply today! As a Product Support Representative III, you will handle customer inquiries and complaints, as well as provide product demonstration and training to internal and external customers. You will also be responsible for participating in other product support functions contributing to sales success. As Technical Support Representative III, you must be able to travel up to 50% of the time, including international travel, in order to provide training, troubleshooting, instrument set-up, and demonstrations. You must also have excellent communication skills. | 08/16/2021 |
| 8086 | Immucor Norcross, GA RBC Processing Technologist Bachelor's degree (BS/BA from a four-year college or university). Exp: 1 - 3 years |
We are currently seeking a RBC Processing Technologist to join our Red Blood Cell Processing team. In this role you will process red blood cells, formulate red blood cell products into a diluted (bulk) state, and perform in-process testing in an aseptic production environment.If you’ve got the necessary skills and experience to excel in this position, we want to hear from you. Apply today! As a RBC ProcessingTechnologist, you will perform a variety of activities in the Red Blood Cell Processing Department. Process red blood cells, formulate red blood cell products into a diluted (bulk) state, and per in-process testing in an aseptic production environment. The incumbent will also perform production tasks in a cleanroom environment in compliance with Good Manufacturing Practices and Good Documentation Practices. | 08/16/2021 |
| 8087 | Immucor Norcross, GA Production Technologist (Monoclonal) Bachelor’s or Associate in Biology, Microbiology, Cell Biology or Chemistry . Exp: 1 year |
We are seeking capable and reliable Production Technologists to join our Monoclonal team. In this position, you will perform basic maintenance on cell culture bioreactor systems. This will involve working with peristaltic pumps and implementing process changes as needed to maximize efficiency and productivity. If you are ready to join an organization where your talents and expertise will be highly rewarded, and if you meet our qualifications to excel in this position, we want to hear from you. This position pays $22 per hour! Contact us today! As a Monoclonal Production Technologist, you will play a key role in the on-going planned maintenance of Hybridoma cell cultures in accordance to established procedures. You will also coordinate subsequent testing and processing of culture supernates to intermediate material for further manufacturing use. | 08/16/2021 |
| 8088 | Cellular Technology Limited [Immunospot] Cleveland, OH Laboratory Technician I (R&D) Laboratory) Bachelors of Science in Biology or other scientific discipline required. Exp: 1 year |
Under the supervision of the Senior Staff Scientist, the Laboratory Technician I will perform scientific experiments in support of the needs of the R&D Laboratory. This position will be responsible for: Performing laboratory work, including ELISA, ELISPOT and FluoroSpot assays Analysis of experimental data and documentation of research activities through the preparation of detailed scientific reports General maintenance of common equipment and overall cleanliness in the laboratory Participating in R&D meetings through the presentation and discussion of data | 08/16/2021 |
| 8089 | KMC Systems Merrimack, NH Quality Engineer I Bachelor’s degree. Exp: 0 - 2 year’s |
We are currently recruiting for a Quality Engineer I, but we are looking for more than an impressive skill set. We are looking for the type of person who respects others for their knowledge, skills, and experience as individuals and as team members. If you are the type of person who has high integrity and would thrive in an inclusive environment of camaraderie and friendship with your fellow teammates, we’re pretty confident you’ll love it here. Assists in planning, devising and implementing Quality Assurance standards, instructions, and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment for an assigned project or area to assure the highest quality levels and cost‑effective compliance with contractual and company requirements. Participates in the design of electronic, electro‑mechanical, or optical equipment for testing company products or components. | 08/17/2021 |
| 8090 | NeuMoDx Molecular Ann Arbor, MI MANUFACTURING SPECIALIST, REAGENT College Degree (BS/BA) in science or chemistry field. Exp: 1 year |
• Manufacturing Specialists are required to have a strong knowledge of manufacturing methods and techniques, process development experience, work flow understanding, ability to understand formulations and follow recipes and testing protocols for any in-process Quality checks • In this position, Manufacturing Specialists, will maintain manufacturing equipment, create work instructions, train others, often be asked to contribute to or lead projects, be cross functionally trained to work in several areas as needed. • This role requires a self-starter, ability to work independently, understanding of departmental goals-working as a team to achieve those goals within set timelines. | 08/17/2021 |
| 8091 | Osiris Therapeutics [Smith +Nephew] Memphis, TN Product Development Engineer I Bachelor’s Degree in Engineering required; Mechanical, Biomechanical or Biomedical preferred . Exp: 0 - 2 year |
With guidance from more senior colleagues or management, this position is responsible for the design, development, verification, and validation of new products from concept phase through design transfer, production, and launch phases using the processes and tools identified in the S&N Quality System related to Design Controls. This position is a functional member of a cross-functional project team working with marketing, manufacturing, quality, regulatory and other team members as appropriate to facilitate the requirements of the design project. | 08/17/2021 |
| 8092 | Osiris Therapeutics [Smith +Nephew] Memphis, TN Quality Engineer 1 - Complaint Investigation B.S. Engineering/Science or related discipline required. Exp: 0 - 2 years |
The Quality Engineer for Complaint Investigation group is focused on ensuring ASD complies with key US and international regulatory requirements, including: complaints and processing, vigilance reporting, Post Market Surveillance, product safety assessments, including Health Hazard Evaluations, Quality Holds and Field Action/Recall implementation. | 08/17/2021 |
| 8093 | Osiris Therapeutics [Smith +Nephew] Memphis, TN MDR Quality Engineer I Bachelor’s degree in engineering or equivalent scientific discipline. Exp: 1 year |
Assure product design history files meet the regulatory requirements of Medical Device Regulation (MDR 2017.745), internal quality system and other applicable regulations. Apply knowledge of ISO 14971 Risk Management; IEC 60601-1 Medical Electrical Equipment and collateral standards, IEC 62366 Usability, and IEC 62304 Software Lifecycle; and other applicable standards to sustaining engineering projects. Serve as primary quality representative on one or more EU MDR project teams Ensure risk management documentation is updated in coordination with activities, and interfacing with project team members including engineering, regulatory, marketing, change management, post market surveillance, and production. Produce technical reports to support product changes or quality assurance investigations. Prepare, evaluate and critique technical documentation including design justifications and rationales based on sound scientific or engineering principles. Makes decisions and proposes solutions based on calculated risks identified through data analysis. Evaluate procedures and processes within the quality system to identify areas for improvement. Recommend solutions to identified problem. Coordinate activities with Quality Engineering Management and report regularly on the progress of activities. Participate in meeting departmental goals and objectives; on time project delivery per release project schedule Travel requirement: Occasional domestic travel may be required less than 10% | 08/18/2021 |
| 8094 | Osiris Therapeutics [Smith +Nephew] Oklahoma City, OK Manufacturing Engineer I Bachelor's of Science degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or other appropriate engineering or enginee Exp: one (1) years |
Responsible for the development of manufacturing methods to produce and bring to market advanced technology products. Works under the direction of the Engineering Project Manager in the development of new processes, introduction of new products, cost reduction projects and capital justifications. Iterate with Product Development Engineers while the product is in the early stages of design to offer creative design & production options to address manufacturability and present its anticipated financial impact. Understand the clinical challenges that the product is trying to address and be able to explain how the new system works to others once it is defined. Guide the internal and/or external supplier(s) in systematically developing robust manufacturing processes. (Six Sigma & Lean experience is preferred.) | 08/18/2021 |
| 8095 | PL Developments Piedmont, SC Process Engineer B.S./M.S. in Chemical Engineering, Chemistry or Pharmaceutical Science is required. Exp: 0-5 years |
Sound knowledge of liquid processing, mixing, flow dynamics, engineering and project management is required. | 08/18/2021 |
| 8096 | Tanvex Biopharma San Diego, CA QC Associate, Lab Control & Raw Material - #1346 Bachelor’s degree or advanced degree in chemistry, biology, biochemistry or related life sciences discipline. Exp: 0-3 years’ |
The Quality Control Associate, Lab Control & Raw Materials is responsible for conducting routine and non-routine analyses of raw material and GMP product as assigned using appropriate analytical methods. This position will coordinate sampling, shipping, and testing of raw materials at outside contract laboratory and in-house to ensure data integrity and compliance, and will work with internal departments to ensure timely testing of raw materials for Manufacturing. The QC Associate will also perform assay transfers, validation of analytical methods, and testing product GMP samples as assigned, compile data for documentation of test procedures and preparation of reports, and ensure raw materials program is in compliance per internal SOP and CFRs. Knowledge of Laboratory Information Management System (LIMS) is a must. | 08/19/2021 |
| 8097 | Tanvex Biopharma San Diego, CA Research Associate, Purification Development - #1304 BS or advanced degree in chemical/biochemical engineering, biochemistry, or related scientific discipline. Exp: |
Apply engineering and scientific principles to design and optimize purification and separation processes to enable scale-up and scale down, technology transfer, process characterization, and process validation activities associated with the purification of biopharmaceuticals. Design and perform bench scale experiments such as chromatography, membrane filtration, depth filtration, tangential flow filtration, and viral filtration Leverage statistical design of experiments to characterize process robustness Write and execute process characterization protocols and development experiment plans. Participate in selected aspects of technology transfer into clinical a cGMP manufacturing facility, including definition of bill of materials, batch record drafting/review; serve as a process development representative during selected purification operations; Mfg floor support. Consistently demonstrate scientific soundness and safety in the laboratory. Effectively communicate ideas, project goals and results within purification through written and oral presentation, and occasionally across departments. Author internal reports at appropriate milestones including process validation and characterization reports. | 08/19/2021 |
| 8098 | Tanvex Biopharma San Diego, CA MSAT Associate Engineer - #1294 Bachelor’s or advanced degree in chemical/biochemical engineering, chemistry/biochemistry, biological sciences, or related disciplines. Exp: |
The MSAT Associate Engineer is responsible for assisting with Manufacturing Science and Technology (MSAT) functions in support of cGMP drug substance manufacturing, including transferring, monitoring, troubleshooting and improving drug substance production processes and technologies. This position will collect and perform statistical analysis of manufacturing in-process control and process parameter data to trend process performance; assist in process related deviation investigations, assess impact to product quality, identify root cause and propose corrective and preventative actions. The MSAT Associate Engineer will also assist in the authoring of SOPs and batch records for new process and new technology as needed and collaborates in cross functional activities with development and manufacturing personnel, both internal and external, to support process scale-up, technology transfer, process characterization, and process validation. This position will serve as technical resource on equipment capabilities and troubleshooting, and provide process knowledge and technical support on the manufacturing floor. | 08/19/2021 |
| 8099 | Tanvex Biopharma San Diego, CA Manufacturing Associate, Upstream - #1316 Bachelor's or advanced degree in life sciences or related discipline. Exp: 0-3 years |
Under supervision, this position will perform routine manufacturing activities in GMP manufacturing areas including fermentation and/or cell culture and the associated sub-processes/preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Fundamental knowledge of current biologics regulations and cGMP for drug substance operation are preferred. Employee will set-up, operate, maintain and clean upstream bioprocessing equipment, which include but not limited to fermenter, bioreactor, centrifuge, homogenizer, filtration skid and mixers. The ideal candidate demonstrates good aseptic technique, execute routine batch records, and regularly draft and revise documents such as batch records, SOPs and technical reports. Candidate must be detailed oriented, a strong team player and has ability to collaborate cross functionally. Flexible shift schedule and overtime may be required. | 08/19/2021 |
| 8100 | Tanvex Biopharma San Diego, CA QC Associate, Microbiology - #1345 Bachelor’s of Science degree in the field of molecular biology, chemistry, biochemistry, or a related scientific discipline. Exp: 0-3 years |
This position performs routine environmental monitoring of GMP manufacturing facilities, assists with trending of environmental monitoring data, and performs routine microbiological testing such as endotoxin, bioburden and sterility. The QC Associate assists with writing method validation protocols, reports and SOP(s) for microbiological operations; generates test results and report results for the assigned GMP testing in a timely and compliant manner; and supports investigations as necessary. | 08/19/2021 |
| 8101 | Tanvex Biopharma San Diego, CA QC Associate, Bioassay - #1340 BS or advanced degree in molecular biology, biochemistry or related life sciences discipline. Exp: 0-3 years |
The Quality Control Associate, Bioassay is responsible for routine and non-routine product testing using biochemical methods. Additional responsibilities may include assisting with transferring test methods from development into the QC laboratory and execute method validation. Generate test results and report results for the assigned GMP testing in a timely and compliant manner. Knowledge of performing and validating cell-based assay, immuno-assays, and/or QPCR assays in a GMP environment is essential. | 08/19/2021 |
| 8102 | Utah Medical Products Midvale, UT Quality Engineer Bachelor's degree (BS) from a four-year college or university. Exp: one year |
1. Manages complaint handling system. 2. Schedules, conducts and/or reviews internal quality audits. 3. Maintains records of internal corrective actions, and participates in routine MRB. 4. Participates in review of R&D and manufacturing projects. 5. Gathers, prepares and presents Company Quality Assurance-related reports. 6. As assigned: develops defect criteria for use in existing products/raw materials, analyzes/investigates defect causes, inspects/tests products/raw materials to determine compliance, failure mode, etc., and participates in company-wide quality-improvement efforts. 7. Confers with all levels of management to address QA issues and coordinate activities. 8. Works well with others. 9. Attends work on all scheduled work days and during scheduled work hours, except where otherwise permitted by immediate supervisor or management, in compliance with company attendance policy. Follows all other company policies and procedures, as set forth in the Employee Handbook and elsewhere, regarding employment. 10. Performs all the essential functions of the job independently using own initiative. | 08/19/2021 |
| 8103 | Advanced BioScience Labs Rockville, MD QC Microbiology I - (00325_COMPANY_1.3) B.A. or B.S. degree in microbiology, biology or related scientific field Exp: 1 year |
The QC Analyst - Microbiology position has several responsibilities in the QC group. The analyst will perform environmental monitoring (EM) for particulates and viables in support of cGMP manufacturing which includes several production suites of ISO class 5, 7, and 8 as well as EU Grade A to D in a GMP facility that produces biopharmaceuticals (vaccines, biologics, viral vaccines, monoclonal antibodies, etc.). In addition, monitoring of purified water, and compressed gases systems is required. Additional responsibilities may include EM data review and compilation of data, report writing, and trending of data; investigations, gowning training and annual gowning qualification. | 08/19/2021 |
| 8104 | Abenza San Diego, CA Downstream Process Development Associate I BS degree in biological sciences, chemistry, chemical engineering, biotechnology, biochemistry or related fields. Exp: 1-3 years’ |
Executes experiments in protein recovery and purification process development using column chromatography and various other techniques. Performs process development activities to devise scalable and robust processes on accelerated timelines. Performs process development activities for projects and products in collaboration with other individuals and departments. Assists with technical transfer of downstream purification processes from clients and between Process Development and other internal groups like Cell Line Development and MSAT/MFG. Assists in scale-up calculations for varying scales of the process — up to cGMP scale. Calculates buffer formulations correctly and makes buffers accurately according to protocols. Assists in the documentation of observations and collecting data for analysis. Capable of data management. Capable of identifying trends in data and notifying scientists of possible impacts. Conducts activities in support of production schedules and objectives as directed by senior staff. Maintains records to comply with regulatory requirements and assists with in-process testing. Maintains lab organization and cleanliness by regularly stocking supplies and managing supply inventory. Assembles and autoclaves tubing assemblies. Maintains cleanliness of specific equipment such as AKTA systems and biosafety cabinets. Maintains up-to-date knowledge of quantitative and qualitative analytical methods. Represents Process Development and its activities, as needed, during project team meetings, training, and evaluation of new technologies. As needed, assists with protein purification under cGMP standards for production of clinical trial material. Performs other related duties as assigned. | 08/19/2021 |
| 8105 | Abenza San Diego, CA Upstream Process Development Associate I BS degree in biological sciences, biotechnology, biochemistry or related fields. Exp: 1-3 years’ |
Assists in cell culture production using aseptic techniques and following protocols and procedures. This includes, but is not limited to: Thaw, maintenance, and expansion of cell culture in shake flasks Preparation of Development Cell Banks Inoculation of bioreactors in a rocker or STR at scales of 2 L – 200 L Maintenance of cell cultures by determining cell count, metabolite concentrations, pH, and gassing Performs process development activities to devise scalable and robust processes on accelerated timelines. Performs process development activities for projects and products in collaboration with other individuals and departments. Assists with technical transfer of upstream manufacturing processes from clients and between Process Development and other internal groups like Cell Line Development and MSAT/MFG. Assists in doing scale-up calculations for varying scales of the process — up to cGMP scale. Accurately makes components, media, buffers and other solutions. Assists in the documentation of observations and collecting data for analysis. Participates in data management and the identification of trends in data and the notification of scientists of possible impacts. Conducts activities in support of production schedules and objectives as directed by senior staff. Maintains records to comply with regulatory requirements and assists with in-process testing. Maintains lab organization and cleanliness by regularly stocking supplies and managing supply inventory. Assembles and autoclaves tubing assemblies. Maintains cleanliness of specific equipment such as incubators, biosafety cabinet, and water baths. Maintains up-to-date knowledge of quantitative and qualitative analytical methods. Represents Process Development and its activities as needed during project team meetings, training, and evaluation of new technologies. As needed, assists with protein production under cGMP standards for clinical trial material. Performs other related duties as assigned. | 08/19/2021 |
| 8106 | Abenza San Diego, CA Associate I- QA Batch Release BS degree in a relevant discipline (e.g., chemistry, biological sciences, bioengineering, etc.) Exp: One (1) to three (3) years |
Perform review of production batch records and test records for buffers, master cell banks, intermediates, and drug substance. Perform review of stability data and testing records for drug substance and drug product. Perform review of facility cleaning records and other GMP records related to facility and equipment. Perform line/room clearances and support manufacturing needs on the floor. Generate Quality Assurance (QA) disposition forms and Certificate of Analyses. Perform review of analytical method qualification reports and associated test data. Provide support in disposition of raw material used in cGMP manufacturing. Analyze data and documentation to support recommendation for batch disposition. Follow SOPs and documents to work in accordance with cGMPs. Write and revise SOPs, qualification protocols, specifications, test methods and reports. Initiate and participate in the investigations for manufacturing deviations. Initiate and participate in the investigations into environmental monitoring excursions to assess any potential impact to product. | 08/19/2021 |
| 8107 | Abenza Bristol, PA AMD/QC Scientist (Biologics) MS or with PhD degree in analytical chemistry, chemistry, biology, biochemistry, or related discipline . Exp: 1-3 years |
Looking for experience with Biologics Method Development of SEC, CE-SDS, SDS-PAGE, and LC-MS. The principle responsibility of the Analytical Method Development/Quality Control (AMD/QC) Analytical Scientist I is analytical support for GMP manufacturing and process development. The AMD/QC Analytical Scientist I may also provide analytical services for discovery and R&D projects as needed. This is a hands-on laboratory position with additional technical responsibilities dependent on experience and expertise. | 08/19/2021 |
| 8108 | Abenza Bristol, PA AMD/QC Scientist (Large Molecules) MS or with PhD degree in analytical chemistry, chemistry, biology, biochemistry, or related discipline . Exp: 1-3 years |
Looking for experience with Biologics Analytical Method Development in SEC, CE-SDS, and UV-Vis. The principle responsibility of the Analytical Method Development/Quality Control (AMD/QC) Analytical Scientist I is analytical support for GMP manufacturing and process development. The AMD/QC Analytical Scientist I may also provide analytical services for discovery and R&D projects as needed. This is a hands-on laboratory position with additional technical responsibilities dependent on experience and expertise. | 08/19/2021 |
| 8109 | Abenza Bristol, PA AMD/QC Associate BS/BA in chemistry, biology or related field. Exp: 0-2 years |
Serves as primary AMD/QC contact for sample receipt, check-in and out, labeling, and inventory management. Coordinates and schedules internal and external testing to ensure committed project deadlines are met. Serves as primary point of contact for external testing facilities. Collects laboratory test results from outside labs and distributes them within the AMD/QC department. Obtains quotations from contract laboratories, fills out purchasing requests forms, and obtains approval from AMD/QC management for outsourced work. Follows/tracks sample shipments. Reviews and evaluates temperature data reports from temperature monitoring devices included with sample shipments. Effectively communicates with other departments to address sample and testing needs. Reports non-conforming events and participate in investigations. Performs daily checks of equipment (e.g.: balances, storage chambers) and chemicals in the AMD/QC lab and appropriately disposes expired reagents. Coordinates with the Facilities department and with service providers for calibration and maintenance of the laboratory instruments in the AMD/QC lab. Analyzes the pH, conductivity, osmolality, and concentration of samples submitted to the AMD/QC lab. Prepares buffers and solutions used in the AMD/QC laboratory. Records his/her laboratory activities in logbooks and laboratory notebooks by following current good documentation practices (cGDP). Complies with current good manufacturing practices (cGMP) and all other regulatory requirements. | 08/19/2021 |
| 8110 | Abenza Bristol, PA Bioconjugation Scientist MS or Ph.D. in biochemistry, chemistry, protein chemistry or related discipline. Exp: 1-5+ years |
Responsible for contributing to the optimization and development of bioconjugation techniques and related processes, including but not limited to the areas of Antibody Drug Conjugates (ADCs), protein drug conjugates, conjugated vaccine, Fluorescent-Probe Bioconjugation and Protein-Protein cross-linking. | 08/19/2021 |
| 8111 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree in biological sciences. Exp: 0-2 years |
The responsibilities of this position are to work on the validation of antibodies for immunocytochemistry applications by making chemical solutions, culturing cells, extensive problem solving and troubleshooting, evaluating cell and tissue staining under the microscope, collecting digital images, and creating reports. | 08/19/2021 |
| 8112 | Advanced Cell Diagnostics Newark, CA Research Associate, Pharma Assay Service B.S. or M.S. in life sciences and/or in molecular biology, biochemistry, cell biology or related field. Exp: 1-2 years |
This position will serve as key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic clients. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. The Research Associate must be willing to learn new techniques quickly and be able to adapt to shifting priorities in a fast-paced and growing start-up environment. This position will be based in Newark, California. | 08/19/2021 |
| 8113 | Advanced Cell Diagnostics Newark, CA Research Associate, R&D BS in molecular biology, biochemistry, cell biology or related field. Exp: 1 year |
We seek a highly motivated and creative research associate to join our R&D team. You will work within a highly dynamic group and be responsible for improving current products and developing new products based on RNAscope technology. Key Responsibilities: Execute RNAscope/BaseScope-based assays to support new product development and assay optimization. Help with fluorescent and bright field slide scanning, scanner maintenance and data processing. Responsible for experimental design, assay running, data collection and interpretation. Maintain sample inventory and logs for slides. Compile and present data to the project team or other departments. Help with lab communal duties. | 08/19/2021 |
| 8114 | Advanced Cell Diagnostics Wallingford, CT Research Associate Assay Development Master’s degree in Chemistry, Biology, or equivalent. Exp: 0 to 2 years |
An exciting opportunity to join a rapidly growing Bio Technology company. Work with a team of scientists to develop high quality immunoassay products for the Simple Plex department. As part of the Simple Plex Assay Development team you will be working towards creating novel commercial immunoassays, optimization of components, developing manufacturing procedures, and performing necessary troubleshooting. The team you will join is fresh, passionate and energetic, and you will have the collaborative support from experienced leadership and a helpful team. | 08/19/2021 |
| 8115 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Conjugation Master’s Degree in chemistry, biological sciences or equivalent required (chemistry or biochemistry preferred). Exp: 0 to 2 years |
Bio-Techne is committed to product quality, customer satisfaction, continued improvement, minimising environmental impacts and conserving natural resources. Environmental and quality management is an integral core value and vital part of the Bio-Techne culture. Position Summary: This position is responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel. | 08/19/2021 |
| 8116 | Advanced Cell Diagnostics Newark, CA Research Associate - PAS B.S. or M.S. in life sciences and/or in molecular biology, biochemistry, cell biology or related field. Exp: 1-2 years |
Advanced Cell Diagnostics, Inc. (ACD), a Bio-Techne brand, is a leader in the field of molecular pathology and tissue-based diagnostics. Our core RNAscope® technology is the world’s first multiplex fluorescent and chromogenic in situ hybridization platform capable of detecting and quantifying RNA biomarkers in situ at single molecule sensitivity. RNAscope® is an ideal platform for developing the next generation of tissue-based companion diagnostics. We are committed to continued innovation to bridge the gap between basic research and clinical medicine to fulfill the promise of personalized medicine. Position Summary: This position will serve as key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic clients. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. The Research Associate must be willing to learn new techniques quickly and be able to adapt to shifting priorities in a fast-paced and growing start-up environment. This position will be based in Newark, California. | 08/19/20921 |
| 8117 | AGTC Gainesville Area, FL R&D Associate B.S. in biological sciences or related field. Exp: one (1) year |
The R&D Associate on the Assay Development Preclinical R&D team is responsible for support of the Assay Development team by developing, qualifying and troubleshooting quantitative, semi-quantitative, and qualitative assays in support of research, nonclinical, and clinical programs. | 08/19/2021 |
| 8118 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Associate I - 1st Shift Bachelors in a science or engineering discipline preferred. Exp: zero to two (2) years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 08/19/2021 |
| 8119 | Ajinomoto Bio-Pharma Services San Diego, CA MQA Associate I Bachelor’s degree strongly preferred in a Life Sciences discipline or equivalent experience. Exp: Zero to two (0-2) years |
We are currently seeking multiple MQA Associate I teammates to join on both 1st and 2nd shift! In this role, you will provide QA oversight and support during manufacturing operations. The Associate I performs documentation review and ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. The Associate I promotes a cGMP environment and collaborates with internal team members to ensure compliance to specifications, processes, and procedures. | 08/19/2021 |
| 8120 | Ajinomoto Bio-Pharma Services San Diego, CA Process Science Associate I - Upstream Bachelor’s degree in a life science discipline or equivalent required. Exp: 0 years |
We are currently seeking Process Science Associate I – Upstream. In this role, you will assist with developing, optimizing and scaling up upstream manufacturing processes for large-scale plasmid and protein production. | 08/19/2021 |
| 8121 | Ajinomoto Bio-Pharma Services San Diego, CA QC Chemistry Associate I Bachelor’s degree in a Life Sciences discipline or equivalent required. Exp: 0 - 2 years |
We are currently seeking a QC Chemistry Associate I. This position is responsible for conducting routine analysis of in process, release and stability assays for proteins, peptides and small molecules under general supervision. The role may focus in a specialized area and perform routine and non-routine analysis with methods such as pH, Density, Viscosity, Conductivity, Appearance, Moisture Content, Particle Analysis, SDS-PAGE, ELISA, Agarose Gel Electrophoresis (AGE), CE-SDS, and Extractable Volume. | 08/19/2021 |
| 8122 | Ajinomoto Bio-Pharma Services San Diego, CA QC Raw Materials Associate I Bachelor’s degree in a Life Sciences discipline or equivalent required. Exp: Zero to two (0-2) years |
We are currently seeking a QC Raw Materials Associate who is responsible for conducting routine analysis, inspection, testing and release of raw materials and Active Pharmaceutical Ingredients (APIs) under supervision. The QC Associate I may focus in a specialized area and provide support in any of the following areas: incoming material inspection and sampling, inspection of vials and stoppers for defects, test method qualification, material qualification, dimensional analysis of components, chemical identification or other lab tests, inspection of commercial packaging materials, lab cleaning and maintenance, maintenance of QC files and paperwork. | 08/19/2021 |
| 8123 | Akebia Cambridge, MA Research Associate II, Cell and Molecular Biology MS in Cell Biology, Molecular Biology, Immunology, or related field. Exp: 0-2 years |
We are seeking a motivated Research Associate to join the biology team to perform cellular/biochemical assays for the identification and characterization of novel small molecules to advance research programs towards clinical translation. This is a lab-based, hands-on position for a scientist looking to be an integral part of drug discovery teams and contributing by delivering high quality in vitro data in a time bound manner. | 08/19/2021 |
| 8124 | American Regent Columbus, OH QC Microbiologist I Bachelor’s degree in Microbiology, Biology, or equivalent Life Science curriculum required. Exp: One year |
This position in the Microbiology Laboratory will be primarily responsible for performing, coordinating and tracking the microbiological testing for in-process and finished products as well as monitoring of controlled manufacturing facilities and utility systems. | 08/19/2021 |
| 8125 | Ampac Analyical Rancho Cordova, CA Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Exp: One (1) to two (2) years |
We are looking for enthusiastic Chemists to join our QC Team in Rancho Cordova (Greater Sacramento area)! QC Chemist Duties: Must use independent judgment to analyze and make determinations as to the quality of a product, using analytical equipment pertinent to the appropriate application of skills. Use various laboratory procedures related to analysis of bulk and pharmaceutical chemicals. Perform analysis of samples using various laboratory equipment and techniques such as FT-IR, Loss On Drying, Non-volatile Residue, Titrations, moisture analysis by Karl Fischer, in addition to other methods. Operate LC and GC systems in order to complete analyses of various types of samples. Maintain a thorough and neat laboratory notebook. Troubleshoot fixes for various instruments in the laboratory. May perform peer review of various commercial product laboratory data. The position uses critical thinking and understanding of highly specialized analytical equipment and chemical compatibility to accurately and safely analyze chemical entities in order to make a determination of the quality of manufactured pharmaceutical compounds. Equipment used: Analytical laboratory equipment. Use of chemical laboratory process and test equipment, specialized analytical equipment and various computer systems. Work place may include areas where a wide variety of chemical materials are used and stored. May involve potential exposure to variable noise levels. Must have a high consciousness for personal and equipment safety. The QC Laboratory runs 24/7/365, so candidates must be open to working all shifts. | 08/19/2021 |
| 8126 | Ampac Analytical Petersburg, VA Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Exp: Zero (0) to two (2) years |
We are looking for enthusiastic Chemists to join our QC Team in Peteresburg, VA (Greater Richmond area)! QC Chemist Duties: This position requires utilization of independent judgement to analyze raw materials, in-process, intermediate and final product, stability, and microbiology samples for the pharmaceutical industry, using various validated methodology as well as experimental ones. The position uses critical thinking and understanding of highly specialized analytical equipment and chemical compatibility to accurately and safely analyze chemical entities in order to make a determination of the quality of manufactured pharmaceutical compounds. Workplace may include working in a variety of areas where chemicals are used and stored. The use of personal protective equipment (PPE) is required. Must use of independent judgment in this salaried exempt position to analyze and make determinations as to the quality of a product, using analytical equipment pertinent to the appropriate application of skills. Use various laboratory procedures related to analysis of bulk and pharmaceutical chemicals. Perform analysis of samples using various laboratory equipment and techniques such as FT-IR, Loss On Drying, Non-volatile Residue, Titrations, moisture analysis by Karl Fischer, in addition to other methods. Operate LC and GC systems in order to complete analyses of various types of samples. Maintain a thorough and neat laboratory notebook. Troubleshoot fixes for various instruments in the laboratory. May perform peer review of various commercial product laboratory data. Equipment used: Analytical laboratory equipment. Use of chemical laboratory process and test equipment, specialized analytical equipment and various computer systems. Work place may include areas where a wide variety of chemical materials are used and stored. May involve potential exposure to variable noise levels. Must have a high consciousness for personal and equipment safety. The QC Laboratory runs 24/7/365, so candidates must be open to working all shifts (12 hour) and possibly one day on the weekend. | 08/19/2021 |
| 8127 | Ampac Analytical Petersburg, VA Process Scientist Bachelor’s, Master’s or Ph.D. degree in Organic Chemistry required. Exp: Zero (0) to two (2) years |
We are looking for enthusiastic Scientists to join our R&D Team! We have opportunities at our Petersburg, VA - Greater Richmond VA Area location. The Process Scientist position is responsible for production support and process development of pharmaceutical ingredients: Develops scalable manufacturing processes in an cGMP environment Conducts experiments to optimize processes for commercial manufacture Meets with groups internally and externally for project meetings and prepares data for presentations Effectively participates in Process R&D team meetings Works under supervision of more senior scientists or scientific directors to advance the company pipeline Thinks critically and creatively and is able to work independently and in interdisciplinary groups Ability to resolve problems and has strong organizational and planning skills * Demonstrates excellent writing and communication skills (both verbal and technical) and strong interpersonal skills. | 08/19/2021 |
| 8128 | BillionToOne West Menlo Park, CA Research Associate BS or MS in Molecular and Cell Biology, Microbiology, Biophysics, Biochemistry, or related field. Exp: 1-2 years |
Do you want to help develop prenatal and oncology diagnostics that can affect the lives of millions of patients? BillionToOne (ranked at the top 5% of Y Combinator companies) is currently seeking a research associate to join our interdisciplinary and innovative R&D team and help us develop novel molecular diagnostics. This person will be responsible for helping to design and performing the molecular assays and experiments under the supervision of our senior research team. This is a dynamic, start-up environment that requires adaptability and the ability to quickly learn and apply new concepts. | 08/20/2021 |
| 8129 | BillionToOne West Menlo Park, CA Laboratory Technician Bachelor’s degree or equivalent in biology or clinical related sciences. Exp: 6 months |
BillionToOne (Y Combinator S17) is looking for Laboratory Technicians - Clinical Laboratory Associates (CLA) - to help perform UNITY, the only non-invasive prenatal test that can detect inherited disorders such as sickle cell disease, spinal muscular atrophy, and cystic fibrosis in the baby directly from maternal blood. You will join our growing superstar CLIA team responsible for the processing of pregnancy blood samples in a high complexity CLIA setting. BillionToOne is a fast-moving and extremely high-growth startup with an important mission. This is a full-time position with an hourly rate of $25/hr with full healthcare (medical, dental, vision, life) and other employee benefits, e.g., 401(k) with matching, as well as career growth opportunities to more senior positions. Hours and days may vary depending upon operational needs. The CLA I is responsible for assisting with the day-to-day operations and equipment maintenance in the Clinical Laboratory. The CLA I will also be responsible for the pre-analytical phase of testing (e.g., specimen receipt, accessioning, and plasma/buffy coat isolation), performing quality assurance procedures, and complying with all local, state, and federal laboratory requirements. | 08/20/2021 |
| 8130 | ArcherDx Boulder, CO NGS Laboratory Technologist (ADX-23-21) Bachelor’s degree in a science-related field required. Exp: Level I: 1 - 3 years |
Executes test methods to evaluate quality, functionality and stability of raw materials, in-process materials and finished products to ensure that they are in compliance with specifications for use in Good Manufacturing Practice (GMP) applications for In-Vitro Diagnostics (IVD). Tracks and identifies trends in QC data and recommends corrective actions when necessary. Assists in method transfer, method validation and method troubleshooting activities. Conducts out-of-specification (OOS)/out-of-trend (OOT) investigations as needed. Lead and support process improvement projects within all QC laboratories ensuring harmonization between the three labs. This position reports to the QC Supervisor, IVD. | 08/20/2021 |
| 8131 | Arcturus Therapeutics San Diego, CA Research Associate I/ II RNA Molecular Biologist/Biochemist Bachelor/Masters degree in molecular biology, biochemistry, or a related field. Exp: 1-2 years |
The Research Associate conducts the following work under supervision: Coordinate with team to define experiments, achieve objectives and execute work following. Synthesize mRNA using in vitro transcription (IVT) system. Process mouse tissue samples for molecular biology analysis (protein, mRNA and DNA extraction). Cell imaging by fluorescence microscopy and imaging analysis. Experience with BSL-2 procedures Perform molecular biology techniques including PCR, cloning, and sequence analysis. Conduct diverse biochemical assays including ELISA, reporter assays, western blotting, and qPCR. Grow and maintain mammalian and bacterial cell cultures. Transfection of DNA and RNA into mammalian cells. Help prepare presentations which summarize procedures, study results, and data interpretation as needed. Deliver high quality results in an accurate and a time sensitive manner. Perform other activities per supervisor’s direction. | 08/20/2021 |
| 8132 | Twist Bioscience South San Francisco, CA Manufacturing Associate Bachelor’s or Associate’s degree in biology, chemistry, biochemistry. Exp: 0-1 year |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate, Library Production will perform molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom molecular biology products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast-paced start-up environment. The Manufacturing Associate will be responsible for the production of custom DNA based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. | 8/7/2021 |
| 8133 | Twist Bioscience South San Francisco, CA Manufacturing Associate Bachelors/ Associates degree in biology, chemistry, biochemistry. Exp: 0-1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate will perform basic molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom gene products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. | 8/7/2021 |
| 8134 | Twist Bioscience South San Francisco, CA Manufacturing Associate (Combinatorial Variant Library) Bachelor or Associates degree in biology, chemistry, biochemistry, or a related field. Exp: 1-2 years |
We are looking for motivated individuals to join our combinatorial variant library (CVL) team in South San Francisco. The Manufacturing Associate will perform library mutagenesis and cloning workflows in a high-throughput manner according to standard operating procedures (SOPs) and will be responsible for the manufacturing and analysis of custom DNA library under production timelines. The ideal candidate will be driven and demonstrates responsibility in keeping manufacturing on track in a fast-paced dynamic environment. The ideal candidate is a team player who can execute well established procedures in a safe and timely manner. | 8/7/2021 |
| 8135 | Twist Bioscience South San Francisco, CA Manufacturing Associate (igG Production) Bachelor or Associates degree or equivalent experience in biology, chemistry, biochemistry. Exp: 0-2 years |
We are looking for an outstanding Manufacturing Associate (MA), to join our team. The Manufacturing Associate will support efforts in developing protein purification expression and purification products. The ideal candidate will be highly motivated and willing to take initiative, learn new techniques, and a desire work in a highly collaborative environment. This position will support projects including high-throughput protein production. The ideal candidate will be eager to learn, be very organized, have excellent molecular biology/biochemistry knowledge and skills, work well on a team, and communicate effectively with peers/management. | 08/07/2021 |
| 8136 | Twist Bioscience South San Francisco, CA Research Associate B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
We are looking for an outstanding Research Associate to join our Specialty Production Team in South San Francisco. The Research Associate will support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast-paced startup environment. The ideal candidate will work independently, be very organized, have excellent molecular biology knowledge and skills, and communicate effectively with peers/management. The Candidate must be comfortable working in a LEAN manufacturing/ controlled laboratory environment. | 08/07/2021 |
| 8137 | Twist Bioscience South San Francisco, CA Research Associate, Specialty Production B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
We are looking for an outstanding Research Associate to join our Specialty Production Team in South San Francisco. The Research Associate will support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast-paced startup environment. The ideal candidate will work independently, be very organized, have excellent molecular biology knowledge and skills, and communicate effectively with peers/management. The Candidate must be comfortable working in a LEAN manufacturing/ controlled laboratory environment. | 08/07/2021 |
| 8138 | United Therapeutics La Jolla, CA Research Associate I - iPSC Bachelor’s degree /Master’s degree in biology, cell biology, or related discipline. Exp: 1+ year |
The Research Associate I, Cell Biology (iPSC) will work in a cross-disciplinary R&D team, in collaboration with internal and external partners, focused on organ manufacturing. Responsible for generation, genome engineering and expansion of human-induced pluripotent stem cells for use in differentiation and cellularization of natural and synthetic scaffolds to create functional human organs. | 08/07/2021 |
| 8139 | Vesigen Therapeutics Cambridge, MA Research Associate I-II, Tissue Culture Core Master’s degree in biology or related discipline. Exp: 1-3 years |
Vesigen Therapeutics is a biotechnology company developing groundbreaking therapeutic products using a unique and fusogenic extracellular vesicle delivery technology directed to intracellular targets. Our ARMMs technology (ARRDC1 Mediated Microvesicles), delivers payloads, including RNAs, proteins, and editing complexes directly into the cytoplasm of target cells. Our team of seasoned drug hunters is committed to leveraging the novel ARMMs technology to develop transformative medicines and address currently unmet medical needs. Vesigen is seeking a creative and highly motivated Research Associate to join our team and help advance the development of the company’s exciting ARMMs technology. The candidate will be an integral member of the R&D team, with opportunities to learn and contribute and develop numerous preclinical programs across several therapeutic areas. | 08/09/2021 |
| 8140 | Vigil Neurosciences Cambridge, MA Research Associate II - Discovery Biology M.S. Exp: 1+ years |
"Founded in 2020, Vigil Neuroscience is a startup biotechnology company taking innovative approaches to treating both rare and common diseases of the Central Nervous System. We focus on developing small and large molecule drugs that can positively modulate neuroinflammation through modifying the biology of the principal innate immune system cell of the CNS, the microglia. We are patient focused and work to develop and test innovative medicines to improve the lives of those suffering from debilitating and lethal neurological conditions. We are looking for a skilled and motivated Research Associate II to join our team. The successful candidate will be responsible for execution of assays for novel therapeutics targeting neuro inflammation, with a primary focus on microglia.The ideal candidate is highly organized, independent, and creative." | 08/09/2021 |
| 8141 | Vir Biotechnology San Francisco, CA TECHNICAL SPECIALIST, LAB OPERATIONS MA/MS/MBA with no experience in a pharmaceutical research or life sciences. Exp: 0 + years |
Vir Biotechnology is seeking a Laboratory Operations Specialist who will work cross-functionally throughout the organization to support general lab activities and safety programs. The Technical Specialist will support the implementation of technologies to drive innovation, efficiency, and productivity in the lab. Additionally, the Technical Specialist will be responsible for vendor relationships and service agreements including maintenance of laboratory facilities and equipment. The candidate must be comfortable working as part of a team, be highly motivated, and display excellent time management skills. | 08/09/2021 |
| 8142 | Vir Biotechnology San Francisco, CA RESEARCH ASSOCIATE I, RESPIRATORY VIROLOGY BS/MS in microbiology, molecular and cell biology, biochemistry or a related field . Exp: 0-2 years |
Vir Bio is seeking a highly motivated and collaborative Research Associate to help drive new efforts in the discovery and development of novel therapies for the treatment of respiratory virus-induced disease. You will work within a highly collaborative group focused on infectious disease research. The successful candidate, under the guidance of experienced Scientists in the company, will participate in discovery and translational research efforts aimed at identifying and characterizing novel therapeutic targets, investigating mechanism of action of therapeutics and defining optimal drug combinations through evaluation in the appropriate in vitro models. You will work cross-functionally and be exposed to other groups within the company to advance programs from discovery into development. | 08/09/2021 |
| 8143 | Vor BioPharma Cambridge, MA Associate Scientist, Process Development MS or equivalent degree in a scientific discipline. Exp: 1+ years |
Vor Biopharma is seeking a motivated Associate Scientist to join our Process Development. The candidate will help drive the development of innovative cell therapy products and platforms, including gene-edited hematopoietic stem cells and allogeneic CAR-T cells. As an integral part of the process development team, this role focuses on developing the manufacturing process for cell therapy products in the immune-oncology space. The successful candidate will plan experiments and generate data to help Vor's leadership make decisions on designing and manufacturing current and future cell therapy products. Working with an interdisciplinary team, the Associate Scientist would gain exposure spanning from research, CMC, regulatory, to GMP manufacturing, and exposure to external CMO and CRO within the space. | 08/10/2021 |
| 8144 | Vor BioPharma Cambridge, MA Associate Scientist, Process Development, Cell Therapy Manufacturing Innovation BS/MS in a science or engineering program. Exp: 1-2 years |
Vor Biopharma is seeking a motivated Associate Scientist/Senior Associate Scientist to join our Process Development - Cell Therapy Manufacturing Innovation group to help drive Vor Biopharma’s manufacturing platform strategies. This matrixed role will help identify needs, develop solutions, conceptualize experimental designs, and execute technology assessments through to implementation towards improving and automating the cell therapy manufacturing workstream. The ideal candidate will have strong wet lab experience with a preference for insights into cell therapies at large (process development, analytical development, and/or cGMP manufacturing and operations). | 08/10/2021 |
| 8145 | Voyager Therapeutics Cambridge, MA Research Associate II/Senior Research Associate, Neuroscience (in vitro) MS in Molecular/Cellular Biology, Biochemistry, Pharmacology or a similar field Exp: 1-3 years |
We are Voyager Therapeutics, a company compelled by curiosity and powered by persistence. We are the seekers who specialize in clinical-stage gene therapy, focused on developing life-changing treatments for severe neurological diseases. Voyager is committed to advancing the field of AAV gene therapy through innovation in vector engineering, capsid discovery, manufacturing, and the optimization of dosing and delivery to enable these novel therapies. Our wholly owned and partnered pipeline focuses on severe neurological diseases, such as Parkinson’s disease, Huntington’s disease, Friedreich’s Ataxia and other areas where patient communities are currently underserved. We’ve been busy, but we’ve got so much more to discover - such is the life of a Voyager. If you’re someone who thrives on finding the elusive answers to tough questions, come explore with us! We are seeking an experienced and highly motivated Research Associate II or Senior Research Associate to contribute to our neuroscience research team at our facility in Cambridge, Massachusetts. This is an ideal position for an individual with a strong background in molecular and cellular assays and methods development, who thrives in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. The successful candidate will be lab based and be responsible for the development, implementation, execution, and analysis of ex vivo and in vitro studies to assess expression, distribution, and pharmacodynamic effects in support of multiple therapeutic programs and platform discovery | 08/10/2021 |
| 8146 | Xellia Pharmecuticals Cleveland, OH Process Engineer (9199) Bachelor’s degree in engineering field. Exp: 0-1 years |
This position is responsible for the planning, coordinating, execution, tracking, and completion of critical aseptic process related projects such as (but not limited to): controlled classified area shut down and restart process, media fill planning and oversight, investigations, smoke studies, aseptic technique evaluation and change control. The Process Engineer serves as a subject matter expert within the aseptic process and is responsible for technical support and supporting the continuous growth of process knowledge at the site. Process improvements will be implemented through use of Lean tools and processes. This position must be able to effectively manage, lead, and problem solve both technically and managerially in a dynamic manufacturing setting. | 08/10/2021 |
| 8147 | Xellia Pharmecuticals Cleveland, OH Microbiologist II (9194) Bachelor’s degree in a Scientific discipline (Microbiology, Biology, Biotechnology, Biochemistry, etc.) or equivalent. Exp: 1 to 3 years |
Our Bedford, OH facility is seeking a Microbiologist II to support the testing in the Microbiology laboratory at the Xellia Cleveland site. In this role, the Microbiologist II is responsible for will be responsible for all aspects of the Microbiology laboratory operations, such as sample receipt, sample testing, data generation, data analysis and summarization and other QC lab supporting activities. Uses good documentation practices in the collection of data/records. Authors and executes qualification documents, SOPs, protocols, and investigations. Recommends corrective actions or process improvements that will eliminate the potential for laboratory deviations. *This position is a flexible 2nd shift position and will include one day per weekend* | 08/10/2021 |
| 8148 | Xellia Pharmecuticals Cleveland, OH Environmental Monitoring Specialist I (9135) Bachelor’s Degree in Microbiology/Science or related field. Exp: 1-5 years |
Our Bedford, OH facility is seeking an Environmental Monitoring Specialist I position works closely with other departments, such as Operations, Maintenance, Quality Assurance, Validation, and Engineering to assure the support of the Environmental Monitoring department on various projects, studies and routine tasks. The individual holding the position of Environmental Monitoring Specialist I shall be responsible for performing routine and non-routine testing. They will be responsible for Environmental Monitoring documentation and corrections. The individual will assist with the training of environmental monitoring personnel on tests and methods. | 08/10/2021 |
| 8149 | Xellia Pharmecuticals Cleveland, OH Environmental Monitoring Specialist I (9136) Bachelor’s Degree in Microbiology/Science or related field. Exp: 1-5 years |
Our Bedford, OH facility is seeking an Environmental Monitoring Specialist I position works closely with other departments, such as Operations, Maintenance, Quality Assurance, Validation, and Engineering to assure the support of the Environmental Monitoring department on various projects, studies and routine tasks. The individual holding the position of Environmental Monitoring Specialist I shall be responsible for performing routine and non-routine testing. They will be responsible for Environmental Monitoring documentation and corrections. The individual will assist with the training of environmental monitoring personnel on tests and methods. | 08/10/2021 |
| 8150 | Xencor Monrovia, CA CON Research Associate 1 A four-year degree is desired. Exp: 6 months to 1 year |
The Research Associate, Discovery Biology and Pharmacology is a temporary role in our Research division. The position is in a dynamic and collaborative environment requiring a sense of urgency, excellent work ethic and the ability to work efficiently and accurately. | 08/10/2021 |
| 8151 | Sekisui Xenotech Kansas City, KS Laboratory Technician or Scientist I Bachelor’s degree in biological or chemical sciences preferred. Exp: 1 year |
SEKISUI XenoTech, LLC is looking to add an entry level Laboratory Technician or Scientist to the Program Execution department! The Laboratory Technician assists with routine laboratory functions including diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintains inventory of supplies, and various other responsibilities. | 08/10/2021 |
| 8152 | Zimmer Biomet Jacksonville, FL Process Engineer (685036) B. S. in Chemical, Mechanical, or Industrial engineering, or other Engineering science. Exp: 0-3 years |
The Process Engineer is responsible for providing engineering services in support of either cellular manufacturing or logistical operations. | 08/10/2021 |
| 8153 | Zymo Research Irvine, CA Bioinformatics Associate master or bachelor's degree in Biology, Bioinformatics, Computer Science, Mathematics, Statistics, or a related discipline. Exp: 1 to 3 or more years |
Zymo Research is seeking a Bioinformatics Associate to join our Bioinformatics team. The qualified individual will play a key role in building, maintaining, and executing data-analysis pipelines for Next-Generation Sequencing methods to support Zymo Research’s global product strategy. | 08/10/2021 |
| 8154 | Zymo Research Irvine, CA Research Associate MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field specifically in the cutting-edge technologies of next-generation sequencing (NGS) and nucleic acids handling. | 08/10/2021 |
| 8155 | Zymo Research Irvine, CA Research Associate - Protein Engineering MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field, developing recombinant proteins and peptides production methods. | 08/10/2021 |
| 8156 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology. Exp: 0-3 years |
The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. | 08/11/2021 |
| 8157 | Affinivax Cambridge, MA QC Analyst, Analytical Chemistry Vaccine Development Bachelor/Master of Science in Biology, Molecular Biology, Biochemistry, Chemistry, or Analytical Chemistry. Exp: 0 to 3 years |
Affinivax has an exciting new opportunity for a QC Analyst, Analytical to join our Quality Control Team to support and contribute to development efforts and ongoing clinical trials. | 08/11/2021 |
| 8158 | Affinivax Cambridge, MA Research Associate 1,2, Fermentation BS in biology, microbiology, or chemical engineering. Exp: 1-3 years |
Affinivax has an exciting new opportunity to join our Product Development team as a Research Associate, Fermentation. This position will report to the Senior Director of Development. | 08/11/2021 |
| 8159 | Affinivax Cambridge, MA Research Associate/Senior Research Associate, Process Development Masters/Bachelors in related fields such as Biochemistry/Biology/Molecular Biology/Chemical Engineering. Exp: 1-5 years' |
Design, manage, and execute studies relevant to process development to advance novel vaccine programs from preclinical through clinical stages. Support and manage process characterization studies. Analyze data from process characterization studies and author reports for internal and external submission, including regulatory agencies such as the FDA. Develop new processes or improve existing processes using scientific expertise, literature review or by seeking inputs from Subject Matter Experts. Provide scientific/technical expertise to develop new Biochemical/ Biophysical methods to support vaccine process development. Understand project timelines/deliverables, support and coordinate cross-functional activities to achieve team and company goals. Document, summarize, and present data to senior management. Additional duties and responsibilities as required. | 08/11/2021 |
| 8160 | Katalyst Healthcares and Life Sciences South Plainfield, NJ Quality Analyst Masters's Exp: 6 months |
Involve in the design, development, implementation, testing, documentation & support of cGxP systems as per 21 CFR Part 11 & US FDA. Responsible for qualification & validation (IQ/OQ/PQ), master plans, protocols, changes requests, gap & root cause analysis, risk management plans, traceability matrix, summary reports for facilities, equipment, systems & processes. Preparation, review, authorize & submission of documentation for quality compliance & regulatory authorities. | 08/12/2021 |
| 8161 | Paraza Pharma Technoparc Montreal, QC Research Assistant-Analytical Chemistry and Purification DEC in Analytical Chemistry Technology or B.Sc. in a similar field. Exp: 0-2 years’ |
The Analytical Chemistry group at Paraza is seeking an energetic, results-oriented individual to join our dynamic team. The successful candidate is expected to take care of the follow up and maintenance of liquid chromatographic systems, as well as, to provide analytical and preparative HPLC support to Medicinal Chemists. The candidate will be expected to work independently within a team structure. | 08/12/2021 |
| 8162 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 08/12/2021 |
| 8163 | Spriaso Salt Lake City, UT Research Chemists Bachelor's degree in chemistry, chemical engineering, biochemistry, or other related degree concentration. Exp: one year |
These positions entails doing product, process, and analytical functions in support of product and technology development under direction of product development and/or analytical leader. The ideal candidate would possess: • Strong computer, scientific, and organizational skills • Excellent communication (oral and written) and attention to detail • Ability to work independently and as part of a team with internal and external clients, self motivation, adaptability, and a positive attitude • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies | 08/12/2021 |
| 8164 | Vaxess Technologies Cambridge, MA Research Associate / Senior Research Associate, In vivo Master’s degree in one of the Life Sciences. Exp: 0-2+ years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials science, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in small animal models to join our core team of scientists and engineers. This is a unique opportunity to be part of an emerging startup bringing innovative technology to the global market. | 08/12/2021 |
| 8165 | Vaxess Technologies Cambridge, MA Manufacturing Engineer BS in Mechanical, Industrial, or Biomedical Engineering, or a related discipline. Exp: 1-2 years |
Research & development at Vaxess is cross-disciplinary, integrating chemistry, biology, immunology, mechanical engineering, biomedical engineering, and chemical engineering to address important unmet medical needs. We are seeking a talented, collaborative, and highly motivated individual with expertise in medical device manufacturing to join our core team of scientists and engineers. This role offers a unique opportunity to build manufacturing capacity from the ground up to bring innovative technology to the global vaccine and therapeutic market. | 08/12/2021 |
| 8166 | Vaxess Technologies Cambridge, MA Engineer I BS or MS in Mechanical, Chemical, Biomedical Engineering, or related discipline. Exp: 0-2+ years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials science, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with experience in process development and medical device characterization. This is a unique opportunity to be part of an emerging startup bringing innovative technologies to the global market. | 08/12/2021 |
| 8167 | AGC Biologics Boulder, CO Process Engineer I/II BS/MS in Engineering (Chemical, Biotechnology, Mechanical, or Electrical) or Master highly preferable. Exp: 1 year |
The Process Engineer I/II primary responsibilities are to support the Colorado manufacturing facility through technical assistance as it relates to manufacturing and process systems. The focus of the role is on ensuring manufacturing equipment, plant utilities and facilities are operating as intended to meet the requirements for biopharmaceutical manufacturing. The Systems Engineering function will provide tactical support of ongoing plant operations and strategic implementation of engineering projects to meet the changing needs of the business. Must be a SME in key critical engineering disciplines (Process, Electrical, Automation, Mechanical, HVAC, etc.) to support the startup, commissioning and lifecycle support of new and existing/legacy systems at the Boulder Colorado manufacturing facility | 08/12/2021 |
| 8168 | AKESOgen Peachtree Corners, GA Research Associate Bachelor’s degree in a clinical, health or life sciences field required. MS preferred. Exp: one year |
This individual is a Research Associate who will work with a team of research associates and scientist at AKESOgen. The Research Associate will work under the general direction of a Team Lead. This individual will perform extractions on a variety of sample types, genotyping on Affymetrix and/or Illumina platform equipment maintenance, solution and reagent preparation in addition to other tasks in laboratory. All duties are subject to change by managers during employment. The following is an outline and is not intended to be inclusive of all tasks that could be requested of employee. | 08/12/2021 |
| 8169 | Amphastar Pharmaceuticals Rancho Cucamonga, CA Production Process Engineer Bachelor's degree (Bachelor of Science) from a four-year College or University in Chemical Engineering or other relevant scientific field. Exp: One to two years |
Research and evaluate new technology and design related to new equipment, process scale up and process improvement. Identify critical to quality attributes of the process and perform experiments to study the process control with the aim of optimizing the process at various stages in its product life cycle. Achieve the corporate target and ensure smooth process development and transfer for the commercial scale production. | 08/12/2021 |
| 8170 | Nitto Denko Avecia Milford, MA Process Development Research Associate-Sr Scientist-level TBD (2821) BS-PhD depending on level. Exp: 0-10+ years |
The responsibilities will change based on level-we currently have entry level to sr. level openings Develops processes and methods for the synthesis, purification, ultrafiltration, lyophilization, and testing of new and existing oligonucleotide products. Participates in the testing and implementation of new work processes, technologies, and procedures. May be involved in product scale-up, process optimization, and validation activities. Maintains up-to-date knowledge of oligonucleotide principles, theories, and processes. Reports status of assigned activities to project teams and to Process Development leadership. Normally works independently in consultation with Process Development leadership. | 08/13/2021 |
| 8171 | Nitto Denko Avecia Marlborough, MA Research Chemist (2021) BA/BS/MS Exp: 1+ years - BS; 0+ years - MS |
The Research Chemist is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. | 08/13/2021 |
| 8172 | Nitto Denko Avecia Marlborough, MA Research Scientist-Level TBD (2162) RS I - MS Exp: 1+ year |
The Research Scientist-level TBD is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. | 08/13/2021 |
| 8173 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry. Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 08/13/2021 |
| 8174 | CRISPR Therapeutics Cambridge, MA Research Associate I/II Master's degree in Life Sciences. Exp: 0 + years |
We are seeking a Research Associate or Senior Research Associate to join an exciting, fast-growing, and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will conduct routine molecular biology protocols in support of in-house sample assays and will participate in development of new next-generation sequencing (NGS) assays for sequence determination, editing efficiency analysis and off-target assessment. The successful candidate will assist in designing, performing, and analyzing experiments for multiple preclinical and clinical programs, and will evaluate and/or implement new analytical techniques and technologies. | 08/13/2021 |
| 8175 | CRISPR Therapeutics Cambridge, MA Research Associate I/II, Analytical Development MS in biological sciences. Exp: 1+ years |
We are seeking a Research Associate I/II to join an exciting, fast-growing, and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work to support process development, product characterization, and technical transfer to CMOs and GMP test labs. | 08/13/2021 |
| 8176 | CRISPR Therapeutics Cambridge, MA Research Associate I/II, Analytical Development MS in biological sciences. Exp: 1+ years |
We are seeking a Research Associate I/II to join an exciting, fast-growing, and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work to support process development, product characterization, and technical transfer to CMOs and GMP test labs. | 08/13/2021 |
| 8177 | CRISPR Therapeutics Cambridge, MA Research Associate I/II, Cellular Biology BS in life sciences or related discipline. Exp: 1+ years |
We are seeking a highly motivated Research Associate I or Research Associate -II to join an exciting initiative to develop gene editing approaches for the treatment of serious diseases. The successful candidate will join the Cellular Biology team within our Editing Technologies group, focusing on cell line engineering for the development of novel gene-editing technologies to support our in vivo and ex vivo therapeutic programs. The successful candidate will be integral to advancing our gene editing platform for CRISPR Therapeutics’ cell and gene therapy programs. | 08/13/2021 |
| 8178 | CRISPR Therapeutics Cambridge, MA Research Associate, Protein Sciences BS or MS in biology or related discipline. Exp: 1+years |
We are seeking a Research Associate to join the Protein Sciences Team within the Editing Technologies group at CRISPR Therapeutics. The successful candidate will play an integral role in developing CRISPR-based gene editing therapies by assisting in the purification and characterization of gene-editing proteins and other proteins of therapeutic interest and examining protein function with various biochemical and biophysical assays. | 08/13/2021 |
| 8179 | Cugene [Rilas Technologies] Woburn, MA Associate Scientist MS in the field of chemistry/chemical engineering Exp: 0 to 3 years |
Rilas Technologies, Inc. is a contract research organization (CRO) founded to provide purification and analytical solutions for the biotech community. The Associate Scientist will work at our lab in Woburn, MA mainly focusing on preparative and analytical HPLC/MS. The ideal candidate will have small molecule purification experience and have an ability to work efficiently and independently. This position requires a self starter who enjoys creative problem solving with excellent written and oral presentation skills, and brings an attention to detail that will maintain and improve the quality of Rilas’ services. | 08/13/2021 |
| 8180 | Cugene [Leukocare Inc.] Milford, MA Technician R&D BS in biotechnology, chemistry, biology, pharmacy or or equivalent education. Exp: 1-3 years |
Primary Responsibilities: Reporting to the Team Lead R&D, you execute project activities related to protein formulation development in the lab: Prepare formulation buffers Perform analytical test methods, e.g., pH, osmolality, HPLC, capillary electrophoresis Perform short-term stability studies You document your experiments according to Leukocare’s quality management system. You are responsible for equipment maintenance and qualification. You conduct day to day lab operations. | 08/13/2021 |
| 8181 | Blueprint Medicines Cambridge, MA Research Associate/Senior Research Associate, Compound Management A Bachelor’s degree. Exp: 1 year |
Blueprint Medicines is looking for a highly motivated individual to be a key contributor in the Compound Management Group. The successful candidate will be primarily responsible for processing new compounds and inventory requests through the Compound Management workflows. | 08/13/2021 |
| 8182 | BioPharmGuy Anytown, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to do some drug pipeline confirmation. This task consists of going to company pipelines pages and making sure the information we list is still accurate. Should have some knowledge of how diseases are categoprized. Must be able to accept payment via PayPal. If interested, send a message through the contact form. Thanks! | 07/30/21 |
| 8183 | Aether Biomachines Menlo Park, CA Lab Assistant (Automation) Associates or Bachelor's Exp: 6-12 mo |
Assist in managing and maintaining Aether's enzyme and compound inventory; Assist in maintaining automation consumables for our factory; Assist in maintaining SOPs as needed to support these processes; Assist with maintenance of state of the art laboratory equipment; Comply with all safety policies and procedures; Operate and support running of high throughput enzyme engineering workflows in our factory; Making media; Setup up runs for the autoclave; Recording data from our instruments and systems. | 08/11/21 |
| 8184 | Scanogen Baltimore, MD CHEMICAL AND BIOMOLECULAR ENGINEER Chemical Engineering degree. Exp: 1+ years |
JOB SUMMARY: The main focus is to optimize and automate biomolecule detection assays JOB DUTIES: • Optimize operations such as cell lysis and DNA hybridization • Optimize PCR-free nucleic acid detection protocols • Collaborate in the design of disposable cartridges that include all the steps of sample preparation and detection • Test disposable cartridge prototypes | 8/2/2021 |
| 8185 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science. Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 8/2/2021 |
| 8186 | SDIX Newark, DE Biotechnician I BS/BA degree in biology, chemistry, or related field such as veterinarian studies. Exp: 0 to 3 years |
Maintain laboratory in proper working order through organization and procurement of supplies, routine maintenance of laboratory equipment, organization and maintenance of reagents, and general laboratory hygiene. Verify and ensure that proper processes and procedures are followed in accordance with SOPs. Support manufacturing aspects of SDIX’s products by executing protocols, utilizing basic knowledge of biology, chemistry, laboratory equipment and computer software. | 8/3/2021 |
| 8187 | SeraCare Life Sciences Gaithersburg, MD Research Associate II – Antibody Purification and Conjugation A recent master’s degree in Biochemistry or Molecular Biology or a related field within the last year. Exp: 1+ years |
Advance Clinical Diagnostics purpose of understanding disease by supporting the research and development of new precision diagnostic products. Support includes independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material. | 08/04/2021 |
| 8188 | SeraCare Life Sciences Gaithersburg, MD Research Associate II – R & D A recent master’s degree in Biochemistry or Molecular Biology or a related field within the last year. Exp: 1+ years |
Advance LGC CDx’s purpose of understanding disease by supporting the research and development of new precision diagnostic products. Support includes independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material. | 08/04/2021 |
| 8189 | SeraCare Life Sciences Gaithersburg, MD Research Associate II – R & D - Master's Level, New Grad A recent master’s degree in Biochemistry or Molecular Biology or a related field within the last year. Exp: 1+ years |
Advance LGC CDx’s purpose of understanding disease by supporting the research and development of new precision diagnostic products. Support includes independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material. | 08/04/2021 |
| 8190 | Seran Bend, OR Manufacturing Engineer I Bachelor of Science degree in an Engineering discipline. Exp: Entry-level |
We currently are seeking an entry-level Manufacturing Engineer I to join Serán’s expanding GMP clinical manufacturing team. The manufacturing team plays a critical role in bringing novel therapeutics to patients with unmet clinical needs. Manufacturing Engineers are responsible for cleaning, assembling, and system testing equipment; execution of complex manufacturing processes in a clean room environment; participating in Technology Transfer exercises; review of batch documentation; and ultimately becoming a Subject Matter Expert on equipment and processes. The Engineer could potentially serve in the role as the technical lead for formulation and process development projects after showing practical hands-on experience with multiple unit operations. Representative unit operations include blending, milling/micronizing, spray drying, dry granulation (e.g., slugging, roller compaction, and milling), wet granulation (e.g., high-shear or fluid-bed), tableting, pan and fluidized-bed tablet/minitablet/bead coating, extrusion (e.g., hot melt or twin-screw wet granulation), and encapsulation. The role of a Manufacturing Engineer at Serán demands an appreciation for, and commitment, to safety, precision, and quality. The Engineer must have a mechanical aptitude, be able to work while wearing appropriate personal protective gear, and occasionally assist with the movement of heavy materials and equipment. | 08/04/2021 |
| 8191 | Seran Bend, OR Scientist / Engineer I Bachelor’s or master’s degree in chemistry, chemical engineering, biology, biological engineering, mechanical engineering, materials science and engin Exp: Entry-level |
Serán seeks to hire an entry-level Scientist or Engineer to contribute to pharmaceutical R&D projects in the general area of drug delivery formulation and manufacturing processes. The successful candidate will work in an interdisciplinary team to develop innovative technical capabilities for the company and support the deployment of these capabilities on programs for Serán’s clients. The role will require both strong hands-on laboratory skills and the ability to apply fundamental scientific principles to define and solve open-ended problem statements. Data analysis and technical communication are also important components of the desired skill set. | 08/04/2021 |
| 8192 | Seres Therapeutics Cambridge, MA Research Associate, Immunology BS/MS in Biology (or equivalent). Exp: 1- 3 years |
At Seres, we’re leading the microbiome revolution — and our most revolutionary asset is our team. Their courage and deep commitment are what drives us on our mission to transform the lives of patients worldwide with revolutionary microbiome therapeutics We are seeking a Research Associate to join the Host Biology team. This person will be responsible for a wide range of experiments with a primary focus in the immuno-oncology and inflammatory disease areas and will also collaborate with the Pharmacology team to support analyses from in vivo studies. | 08/04/2021 |
| 8193 | Sestina Bio Pleasanton, CA RA II/III/SR Bioengineering BS/BA or MS degree. Exp: 1 years |
Sestina Bio is looking for a flexible and talented research associate to join our Biological Engineering group to build world class cellular factories using cutting edge genetic engineering, analytics, and data science technologies. This researcher will work collaboratively with other Bioengineering team members across functions and will be primarily responsible for designing and creating DNA parts, executing strain engineering and selection strategies, preparing samples for analytical evaluation, and helping to develop novel laboratory tools and methodologies. The ideal candidate has experience in yeast strain engineering, general knowledge of cellular metabolism, and some experience working with high throughput sample preparation. We’re looking for a creative, independent applicant with a positive attitude that is excited about quickly modulating metabolic pathways to produce yeast-based products with market leading properties. | 08/04/2021 |
| 8194 | Smithers Gaithersburg, MD Associate Scientist BA/BS in Biological or Physical Sciences. Exp: 6 mos + |
Level of position will be commensurate with experience. Knowledge of GLP regulations and other regulatory guidelines. Excellent communication skills, both oral and written, and strong organizational skills. Proficient in the use of basic computer applications such as MS Word and Excel. Authorization to work in the United States indefinitely without restriction or sponsorship | 08/04/2021 |
| 8195 | Smithers Gaithersburg, MD Scientist MS in biology, life sciences, or chemistry field. Exp: 1 year |
Smithers PDS is seeking a scientist to join our team in Gaithersburg, MD. The Scientist performs data analysis and various assays according to SOP with reliability while applying and meeting GLP, GCP, and/or CLIA requirements. This position assists with ensuring that the lab, materials, and equipment are maintained. | 08/04/2021 |
| 8196 | Smithers West Trenton, NJ Associate Research Scientist MS degree focused on molecular biology. Exp: 1 year |
Smithers Pharmaceutical Development Services is building a state-of-the-art translational science facility in Ewing NJ and is actively seeking an Associate Research Scientist to join our team. The candidate should bring a keen curiosity and desire to take a key role in development, validation, and documentation of novel nucleic acid analysis methods under guidance of a Research Scientist. Experience in tissue culture, RNA and DNA sample preparation, amplification, and characterization is highly desired. This role will also ensure that basic lab management functions such as equipment maintenance and an adequate supply of materials and reagents is maintained. Relocation expenses will not be provided. | 08/05/2021 |
| 8197 | Smithers Gaithersburg, MD Research Scientist for Method Development MS degree focused on molecular biology. Exp: 1-2 years |
Smithers is seeking a talented Associate Research Scientist with expertise in bioanalytical informatics systems including automation platforms. The individual will be responsible for design, development and implementation of automation tools and software solutions to support regulated bioanalysis. | 08/05/2021 |
| 8198 | Solid Biosciences Cambridge, MA Associate Scientist I/II Analytical Development B.S. in Microbiology, Biology, Genetics or related field. Exp: 1+ years |
Solid Biosciences is looking to hire an Associate Scientist I/II in Analytical Development to be responsible for analytical development, qualification and operational support for Preclinical, Phase I through Phase III of clinical products for Solid Biosciences. Solid Biosciences’ leading candidate is an adeno-associates virus (AAV) based gene therapy product for the treatment of Duchenne Muscular Dystrophy (DMD). | 08/05/2021 |
| 8199 | Spherotech Lake Forest, IL Quality Control Associate Bachelor's degree in Chemistry or related field. Exp: 1 year |
Duties include final product inspection, documentation, Quality Control testing etc. | 08/05/2021 |
| 8200 | SRI International Menlo Park, CA Bioscience Research Associate I BS or MS in Organic Chemistry. Exp: 0 - 2 years |
The Applied Research section of the Biosciences Division is looking for a committed and enthusiastic scientist to join our team as a Research Associate in Organic Chemistry. The chemist will have the opportunity to contribute to a range of projects including drug discovery projects, process development and scale up, chemistry automation, and high-throughput synthesis. Our team routinely collaborates with experts from related disciplines including biologists, physicists, chemical and mechanical engineers, computer scientists, and software developers. The Research Associate’s primary responsibility will be the synthesis and characterization of novel compounds for internal programs and with external partners. The RA will be asked to keep diligent laboratory records, participate in project meetings, and assist in maintenance of laboratory equipment.The RA will be expected to work well as part of a team of multidisciplinary scientists and engineers. | 08/05/2021 |
| 8201 | SRI International Menlo Park, CA Bioscience Research Associate II BS in Biology, Biochemistry or related field. Exp: 1 - 2 years |
The Biosciences Division at SRI International is looking for a researcher to join our engineering team for the development of novel fermentation processes. This role will involve operation of bioreactors, performing and validating assays, and documentation of new and existing processes. This position will also offer potential areas for growth in data analysis, analytical method development, hardware design, experimental planning and scale-up operations. The individual would work closely with an interdisciplinary team of biologists, chemists, and engineers to focus on the process development of fermentation products in a number of consumer sectors. We are looking for highly-motivated workers looking to grow and expand their experience. This role is fast-paced and highly interactive and being able to work closely within a team is a must. | 08/05/2021 |
| 8202 | Steri Pharma Syracuse, NY Microbiology Analyst, 1st Shift, Pharma Bachelor’s degree from a regionally accredited institution in science or related field. Exp: 1-3 years’ |
This position performs environmental monitoring of aseptic process area, to include testing of finished products, raw materials, and components according to established procedures. Position applies standard concepts, practices, and procedures within the laboratory. Position performs a variety of tasks. Position will also be responsible for document review. | 08/05/2021 |
| 8203 | Strand Therapeutics Boston, MA Associate Scientist, Molecular Biology M.S. Exp: 1 year |
Strand is looking to build a team that understands the value of working at a start-up. Joining the company now means having vast opportunities to learn and grow including having the exposure to all aspects of building a company. We are looking for people who have the enthusiasm and motivation to be a highly contributing member of a small team. This opportunity will offer the employee the ability to work closely with the founding team, as well as to form close partnerships with team members during the development and formation of the company. We are looking for an Associate Scientist I/II to support our molecular and cell biology needs to enable the drug discovery efforts within the Molecular Biology team at Strand Therapeutics. The ideal candidate will have experience in mammalian cell culture including primary cell isolation and handling. The candidate will be expected to work in an innovative, fast-paced, cross-collaborative biotech environment and contribute in multi-disciplinary team activities to advance our platform. | 08/05/2021 |
| 8204 | Strand Therapeutics Cambridge, MA Associate Scientist, LNP Formulations Development B.S./M.S. in Pharmaceutical Sciences, Chemistry, Chemical Engineering or other relevant scientific discipline. Exp: 1-3 years |
Strand is looking to build a team that understands the value of working at a start-up. Joining the company now means having vast opportunities to learn and grow including having the exposure to all aspects of building a company. We are looking for people who have the enthusiasm and motivation to be a highly contributing member of a small team. This opportunity will offer the employee the ability to work closely with the founding team, as well as to form close partnerships with team members during the development and formation of the company. We are looking for a highly motivated and innovative candidate for the role of Associate Scientist, LNP Formulation Development. The expectation is that the candidate will have experience in formulation and characterization of LNPs (Lipid Nanoparticles). The candidate will be expected to work in an innovative, fast-paced, cross-collaborative biotech environment and contribute in multi-disciplinary team activities to advance our platform. | 08/05/2021 |
| 8205 | Strand Therapeutics Cambridge, MA Associate Scientist, mRNA Process Development BS in Biochemistry, Chemical Engineering, Molecular Biology, Bioengineering, Molecular Medicine, Genetics or related field preferred. Exp: 1-2+ years |
Strand is looking to build a team that understands the value of working at a start-up. Joining the company now means having vast opportunities to learn and grow including having the exposure to all aspects of building a company. We are looking for people who have the enthusiasm and motivation to be a highly contributing member of a small team. This opportunity will offer the employee the ability to work closely with the founding team, as well as to form close partnerships with team members during the development and formation of the company. We are looking for a highly motivated and innovative candidate for the role of Associate Scientist, mRNA Process Development. The expectation is that the Associate Scientist will have experience independently executing mRNA process development experiments and production efforts. Reporting to Scientist, Process Development, the right candidate will be a strategic thinker that brings a leadership presence and enthusiasm for Strand along with a desire to conquer new challenges. | 08/05/2021 |
| 8206 | Sword Diagnostics Chicago, IL Research Associate I BS or BA in biology, biochemistry or related field. Exp: 1 - 3 years |
Plan experiments with guidance from supervisor • Perform complex and critical laboratory experiments (primarily ELISA) with accuracy and precision • Analyze experiment results and recommend potential follow-on experiments • Follow all established company processes and procedures • Prepare buffers and other chemical solutions as needed • Other duties and responsibilities as assigned | 08/05/2021 |
| 8207 | Synlogic Cambridge, MA Process Development Engineer B.S. in Chemical Engineering, Biochemical Engineering, Microbiology or related field. Exp: 1-3 years |
We are currently seeking a highly motivated and enthusiastic Process Development Engineer to contribute to operation and development of microbial fermentation processes for characterization and manufacturing of our novel live biotherapeutics. | 08/05/2021 |
| 8208 | Synlogic Cambridge, MA Research Associate - Bioanalysis BS/MS in Chemistry, Biochemistry, Molecular Biology, or related field. Exp: 1-2 yrs |
Synlogic is seeking a motivated associate with experience in bioanalytical sciences for a position in the Quantitative Biology team. The ideal candidate will have the unique opportunity to actively contribute to Synlogic’s cross-functional metabolic program teams: from early discovery to clinical stages of drug development. This role will contribute to our in-house assay development and implementation to characterize engineered bacterial strains, broadly supporting product development and in vivo pharmacology efforts. The successful candidate will be collaborating with Synthetic Biology, Pharmacology, and Process Development and Manufacturing Sciences teams to advance our Synthetic Biotics pipeline | 08/05/2021 |
| 8209 | Synthego Redwood City, CA Research Associate, Engineered Cells BS in molecular and cell biology or biology-related field. Exp: 1 year |
Synthego is searching for a Research Associate to join our Engineered Cells Operations team and help create the world’s first fully automated Genome Engineering lab. | 08/05/2021 |
| 8210 | Takeda San Diego, CA Research Associate II GI Inflammation BS degree in a scientific discipline, or equivalent. Exp: one year |
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Research Associate - GI Inflammation in our San Diego, CA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. | 08/05/2021 |
| 8211 | Takeda Boston, MA Engineer II Bachelors degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science. Exp: 0-3 years |
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Engineer II in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. | 08/05/2021 |
| 8212 | TCR2 Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Virus Production (Research) B.S./M.S. in a scientific or engineering discipline. Exp: 1-5 years |
We are looking for a Research Associate/Senior Research Associate to provide key support to our Research teams. This position presents a unique learning opportunity to research grade lentivirus production. You will be part of the Virus Production Team (Research) and working in an integral environment with people from Research teams and Process Development teams. You will optimize and execute our internal viral vector manufacturing process and characterize the viral vector products to release them to the Research and Development teams for impactful studies downstream. The position will expose you to several critical aspects of gene therapy: viral vector production, characterization and quality control as well a genetically engineered T cell research and development. | 08/05/2021 |
| 8213 | TCR2 Therapeutics Cambridge, MA Research Associate/Sr. Research Associate, Early Discovery Innovation B.S./M.S. degree in biological sciences. Exp: 1 year |
We are looking for a Research Associate/Sr. Research Associate to join our Innovation team. Reporting to our Sr. Scientist of Early Discovery you will be utilizing cellular assays, immune cell profiling, and molecular biology for the development and optimization of novel cell therapies for the treatment of cancer. This role is an excellent growth and learning opportunity as you will be working closely with experienced scientists in a fast-paced and highly collaborative environment. | 08/05/2021 |
| 8214 | TCR2 Therapeutics Cambridge, MA Research Associate, Upstream Vector Process Development BS in Biochemical Engineering, Chemical Engineering, Biology, or related discipline. Exp: 0-2 years |
We are growing and hiring a Research Associate to join our Process Development team. You will work on the purification of lentiviral vectors, and development of a robust and scalable manufacturing process. This role is a unique opportunity to learn and advance your career development actively working with a close team in a fast-paced and highly collaborative environment. | 08/05/2021 |
| 8215 | TCR2 Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Molecular and Vector Biology B.S./M.S. degree in molecular and cell biology preferred. Exp: 1 year |
We are growing and are looking for a Research Associate/Senior Research Associate to join the Molecular and Vector Biology core. You will report and work closely with our Scientist and will use molecular cloning techniques for the development and optimization of novel cell therapies for the treatment of cancer. The position represents an excellent growth and learning opportunity to learn new techniques, working closely with an experienced team, in a fast-paced and highly collaborative environment. | 08/05/2021 |
| 8216 | Teligent Buena, NJ Microbiologist I BS in Microbiology or related field. Exp: 1-year |
Responsible for Quality Control functions including, conducting physical testing of raw materials, assisting in Document Control of Quality Control Documents and assisting with all Quality Unit needs as they pertain to quality system compliance. | 08/05/2021 |
| 8217 | Tenaya Therapeutics South San Francisco, CA RA I/II Analytical Development BS/MS in a biological science, chemistry or physics. Exp: one year |
We are seeking a motivated Research Associate for our Technical Operations Analytical Development Group. In this role, you will perform key potency, purity and strength assays to support Process Development activities; troubleshoot and optimize particular assays as needed; assist in the development of new analytical methods to determine the strength, purity and/or potency of viral vector preparations; and perform other tasks such as lab equipment maintenance and supply ordering. | 08/05/2021 |
| 8218 | Tenaya Therapeutics South San Francisco, CA RA I/II Downstr PD Bachelor’s or Master’s degree in Biology, Biochemistry, Engineering or related discipline. Exp: 0-3 years |
We are seeking a motivated Research Associate for our Technical Operations, Process Development Group. In this role, you will perform key experiments to support Downstream Process Development; routine bench-scale purifications; troubleshoot and optimize process parameters; onboard new characterization methods to determine precursor and in-process material purity and identity; perform housekeeping tasks such as lab equipment maintenance and supply ordering. The ideal candidate for this role will have assay operation and data analysis experience looking to shift their career track to process development. | 08/05/2021 |
| 8219 | Tenaya Therapeutics South San Francisco, CA Research Associate I, Biology Bachelor or Master degree in Biology, Biochemistry, or related discipline. Exp: 1 years |
Tenaya has an immediate need for a Research Associate I to support the gene therapy team. The ideal candidate is a self-starter and problem-solver who will work closely with the team to drive the company’s future success. Ideally, you thrive in a startup, fast-paced environment where every day is unique. You are confident, poised and cool-headed, no matter how much is changing around you. You strive for excellence in every facet of your work and you understand the excitement and commitment of ‘start-up’ roles. Finally, you love being part of a team aligned around a compelling mission. | 08/05/2021 |
| 8220 | Tenaya Therapeutics South San Francisco, CA Research Associate, In Vivo Research BA/BS/MS in biology, pharmacology or related field. Exp: 1 year |
Develop and validate pathophysiological heart disease models, including surgical or chemical induced and genetically modified models. Perform aseptic surgeries including preparation, surgical procedures, post and daily monitoring. Support in vivo preclinical studies to identify and characterize innovative drug therapies for the treatment of heart failure. Assisting necropsies and ex vivo sample collections, tissue preparations Weighing, Data entry and creating sample labeling and shipping. Creating study forms and sample archiving on Microsoft Word & Excel Conducting animal genotyping, PCR, western blotting, immunofluorescence, and instrumental sample analysis Establishing and maintaining excellent working relationships with critical collaborative partners throughout the company. | 08/05/2021 |
| 8221 | Tenaya Therapeutics South San Francisco, CA Research Associate I/II-Drug Discovery Bachelors or Masters degree in Biology, Biochemistry, or related discipline. Exp: 1 year |
Execute a diverse range of cell-based and biochemical assays to characterize lead molecules and evaluate target function Employ cutting edge molecular, cell, and biochemistry techniques to enhance drug discovery efforts Support new target discovery for genetic cardiomyopathies using iPSC-derived cardiomyocytes Present findings in both small and large group company meetings | 08/05/2021 |
| 8222 | Tessera Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Cell and Molecular Biology B.S./M.S. in biological sciences or related field. Exp: 1 year |
The DNA Editor group is seeking a Research Associate/Senior RA. The role will support the development of novel gene editors to advance programs for proof-of-concept studies. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 08/06/2021 |
| 8223 | Tessera Therapeutics Cambridge, MA Research Associate/Senior Research Associate, LNP Formulation BS/MS in Chemistry, Chemical Engineering, Bioengineering, Pharmaceutical Sciences or related discipline. Exp: 1-2 years |
Tessera Therapeutics is seeking a Research Associate/Senior Research Associate to help support the lipid nanoparticle (LNP) formulation process and produce LNP-encapsulated RNAs and plasmids to support company’s in vitro and in vivo pre-clinical studies. In addition, the successful candidate will support the execution of characterization assays LNP batches. The ideal candidate will be proactive, enthusiastic, and show a passion for process development. The applicant should have strong communication and collaboration skills, along with a strong background in formulation process development and in LNP characterization. | 08/06/2021 |
| 8224 | Tessera Therapeutics Cambridge, MA Research Associate/Senior Research Associate, RNA Production Bachelors degree. Exp: 0-3 year |
Tessera Therapeutics is seeking a Research Associate/Senior Research Associate for high throughput RNA production process. You will support process development for in vitro transcription, modification, and purification of RNAs to support Tessera's pre-clinical efforts. We seek scientists that are proactive, enthusiastic, and show a passion for process development. The successful candidate should have strong communication and collaboration skills. Strong attention to detail and excellent organizational and documentation skills are highly desirable. | 08/06/2021 |
| 8225 | Teva West Chester, PA Biological Researcher I Bachelors degree in Biochemistry, Biology, Biotechnology or a related field, or a Masters degree in above fields. Exp: 1 year |
We are seeking a highly motivated scientist with knowledge of molecular biology and protein biochemistry to support the generation of critical reagents for bioanalytical assays. As a member of team, your responsibilities include but not limited to: Assist DNA constructs design, order DNA synthesis and subclone from external vendors, and prepare plasmid amplification for protein overexpression. Perform overexpression of recombinant proteins in mammalian cell cultures. Perform purification of protein needed for critical reagent generation and bioanalytical assays. Generate critical reagents by protein conjugation to proper ligands. Perform routine reagent analysis and characterization including protein concentration measurement, analytical SEC, SDS-PAGE. Provide complete and compliant documentation (e.g. Certificates of Analysis). Make accurate and timely record and experimental data in ELN and proper databases. Maintain good sample inventory. | 08/06/2021 |
| 8226 | TG Therapeutics Waltham, MA Engineer/Scientist, CMC Biologics Bachelor’s or Master’s degree in chemical/biochemical engineering, biochemistry, or related area. Exp: 1-4 years |
As TG Therapeutics transitions to a commercial operation, the CMC Biologics group in Waltham, MA is expanding to support the biologics pipeline, including commercialization of its lead biologic asset. We are seeking to hire in our upstream group; this position will support process development, technology transfer, validation, and manufacturing. As a virtual company, all work is outsourced so this individual will work with both the internal team and outside vendors. This position will start out remote but transition to working with the team at the Waltham, MA office when public health conditions allow. This is a great opportunity for an early career professional to experience working in a start-up environment, work with managers with decades of experience, and take his/her career to a new level. | 08/06/2021 |
| 8227 | Theravance Biopharma South San Francisco, CA Research Associate II BS/MS in a relevant scientific discipline. Exp: one year |
The department of Biology and Pharmacology is currently seeking a motivated Research Assistant/Associate to participate in drug discovery research. The successful candidate will work collaboratively with senior scientists to develop and execute pharmacodynamic and disease mechanism models designed to assess the pharmacological activity of novel molecules. The successful candidate should have the ability and willingness to work in a variety of therapeutic areas. | 08/06/2021 |
| 8228 | Theravance Biopharma South San Francisco, CA Research Associate I-II, In Vitro Biology/Pharmacology BS/MS in a relevant scientific discipline. Exp: 1-2 years |
We are seeking a Research Associate to join the In Vitro Biology/Pharmacology Department. This individual will join a multi-disciplinary team to develop, automate and conduct biochemical and cell-based assays to help drive lead optimization and obtain mechanistic insights for all research programs. | 08/06/2021 |
| 8229 | Theravance Biopharma South San Francisco, CA Research Associate, DMPK, Temp BS/MS in Chemistry/Biochemistry/Pharmaceutical Science or related coursework . Exp: 1+ years |
The Drug Metabolism and Pharmacokinetics (DMPK) department at Theravance is seeking a laboratory-based research associate for a 6-month assignment supporting small-molecule drug discovery and development. The primary responsibilities will include support of studies related to metabolism and disposition of lead molecules. A background in conducting in-vitro assays (e.g. metabolic stability) and analyzing samples via LC-MS would be desirable. The successful candidate will exhibit strong communication and interpersonal skills and desire to work in a fast-paced, flexible and dynamic environment. | 08/06/2021 |
| 8230 | Theravance Biopharma South San Francisco, CA RA I - SRA, Medicinal Chemistry BS at the RA I level Exp: 1-2 at the RA I level |
As a member of our medicinal chemistry team, you will be responsible for the design, synthesis and optimization of compounds on one of our exciting interdisciplinary drug discovery programs. The successful candidate will be able to interpret biological data and make proposals to influence the direction of the medicinal chemistry strategy. We offer a stimulating, challenging and productive discovery environment with a strong commitment to developing the medicinal chemistry skills of our people. | 08/06/2021 |
| 8231 | Tris Pharma Monmouth Junction, NJ AR&D Scientist - ALL LEVELS Bachelors degree/MS degree in Chemistry or related scientific field. Exp: 1 year |
To support expectations of continued growth Tris is expanding the Laboratories at our Monmouth Junction, NJ facility and has openings for all levels of Analytical Research and Development (AR&D) Scientists. | 08/06/2021 |
| 8232 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate RA04-3 Bachelor’s degree or Master’s degree in Immunology, Cell Biology, or related discipline. Exp: 1-2 years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for an experienced researcher to join our team as Research Associate/Senior Research Associate, supporting our novel target identification and validation workflow in house. The ideal candidate should have relevant experience in primary T cell culture, immunoassays, flow cytometry, and molecular biology, and enjoy fast-paced, collaborative and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 08/06/2021 |
| 8233 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate (RA05-5) M.S. degree in Immunology, Cell Biology, or related discipline. Exp: 1-3 years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for an experienced researcher to join our team as Research Associate or Senior Research Associate, supporting our novel TCR discovery workflow in house. The ideal candidate should have relevant experience in T cell immunology, cancer cell culture and flow cytometry, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a willingness to learn will thrive in this role. | 08/06/2021 |
| 8234 | Pharmaceutics International Hunt Valley, MD Chemist BS in chemistry or related physical / biological science. Exp: 1 or more years |
Plan and perform pharmaceutical analysis activities with minimum supervision and direction. | 7/26/2021 |
| 8235 | Pharmaceutics International Hunt Valley, MD Chemist - QC BA Degree in Chemistry, Pharmacy and/or Pharmaceutics/ Other Sciences required, and masters degree preferred. Exp: 3 months |
Performs tests and analysis of raw materials, bulk, in-process materials, finished products, scale-up samples, process validation samples, cleaning validation samples, and stability samples using a variety of standard and advanced analytical techniques. -Works with the following instruments: HPLC, UPLC, GC, and UV-spectrophotometer. -Prepares technical documentation including test reports; analytical test procedures; and change controls. -Supports systems and procedures to ensure the successful completion of departmental goals and objectives. -Prepares documents to report analytical test results. -Assists Metrologists in laboratory equipment qualifications, calibrations and preventative maintenance programs, as needed. -Manages USP reference standards and the qualification of secondary standards, as needed. -Works to ensure compliance with cGMP, cGLP, ICH, FDA (21 CFR Part 11) and the site operating procedures under the direction of senior staff or laboratory management. -Work on GLP documentation, protocols, SOP revision, investigations, and compendia changes. | 7/26/2021 |
| 8236 | Phitonex [Thermo Fisher] St Louis, MO QC Support Scientist I Bachelor’s degree in a Biological Science or related field. Exp: 1 year |
A support function to the QC Testing group essential functions include writing documents, writing minor deviations, and other non-testing related duties as assigned. | 7/26/2021 |
| 8237 | Phitonex [Thermo Fisher] Greenville, NC QC Scientist I: Raw Materials (1st shift) Bachelor’s degree in physical science, preferably in Chemistry or Biology. Associate degree in Chemistry or Biology related discipline minimally requi Exp: 0-2 years |
Provides routine analyses in a chemistry or microbiology environment by following standard practices. Performs analytical methods as assigned for testing on raw materials, samples, stability, environmental, production intermediates, and/or human cells. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results. Typical hours for this role is 7:30a-4:00p, Monday-Friday with some overtime. | 07/26/2021 |
| 8238 | Phitonex [Thermo Fisher] St Louis, MO Biopharmaceutical Technician I Bachelor’s degree in Biology, Biochemistry or Chemistry seen as a plus. Exp: 1-3 years |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 07/26/2021 |
| 8239 | Phitonex [Thermo Fisher] Carlsbad, CA Protein Manufacturing Associate Master’s degree in Biology, Chemistry, Biochemistry, or other related discipline. Exp: 1+ years |
The successful candidate demonstrates a sense of urgency, contagious optimism and a “can do” attitude. They lead by example and hold themselves and others accountable, while maintaining productive and professional relationships within the team. The primary responsibilities are as follows: Responsible for manufacturing product(s) in a lab setting following standard operating procedures. Will utilize basic laboratory techniques, calculations, materials measurement, operation of laboratory equipment and record keeping necessary to manufacture products. Will perform column purification/ chromatography, buffer preparation, SDS-Page Analysis, Western Blotting, and other protein characterization techniques. Responsible for Batch Data Records, notebooks, customer reports (as required) and work order documents. Utilize specialized technical knowledge and skills to make detailed observations and analyze data to ensure within operating parameters. Advise manager of factors that may affect quality of product. Suggest and execute on options/ideas for corrective actions. Maintain equipment, product inventories and related records as assigned. Note variances on manufacturing documents; audit and evaluate process documents and propose revisions. Complete, distribute and file records as required in accordance with Document Control Practices. | 07/26/2021 |
| 8240 | PlateletBio Watertown, MA Research Associate A B.SC. or M.S. Exp: 1+ years |
We are looking for a motivated candidate who will join Platelet Bio to provide support for in vitro pre-clinical studies on a stem cell-derived therapy for autoimmune diseases. Our ideal candidate is a driven, creative thinker, who is a great team player and shares our long‐term vision and passion for leveraging stem cell-derived therapies to cure diseases. Come join our team today and help make a difference in thousands of patients’ lives. | 07/26/2021 |
| 8241 | PPD Devens, MA ASSOCIATE SCIENTIST - LC , CE , ELISA , BIOLOGICS Bachelor's degree in Biochemistry, Biotechnology, Analytical Chemistry, or equivalent and relevant formal academic / vocational qualification. Exp: 1-2+ years |
As a Associate Scientist, you will be responsible for supporting analytical activities within Biologics Process Development (PD). The role will involve supporting in-process analytical testing, delivering results within customer and project timelines, assay harmonization activities within the network groups, and evaluation of new analytical technologies. You will have excellent communication skills, is a team player, and have experience in Bioanalytical techniques as they apply to Biologics and related process impurities. Techniques of interest include Capillary Electrophoresis, Liquid Chromatography, and ELISAs. A reasonable appreciation of upstream and downstream process development activities is highly desirable. This role will be located in Devens, MA. The role will provide Analytical support within PD. The candidate will work closely with PDA team members and Process Development to deliver quality analytical data in a timely manner. | 07/27/2021 |
| 8242 | PPD Middleton, WI ASSOCIATE SCIENTIST - BIOPHARMACEUTICALS Bachelor's degree (Life Sciences degree preferred) or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
As a Biochemist, referred to as an Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and analysis serve as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. | 07/27/2021 |
| 8243 | PPD Middleton, WI ASSOCIATE SCIENTIST Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ year |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 07/28/2021 |
| 8244 | ProteinSimple [Bio-Techne] Newark, CA Research Associate, R&D A BS in molecular biology, biochemistry, cell biology or related field. Exp: 1 year |
We seek a highly motivated and creative research associate to join our R&D team. You will work within a highly dynamic group and be responsible for improving current products and developing new products based on RNAscope technology. | 07/28/2021 |
| 8245 | ProteinSimple [Bio-Techne] Minneapolis, MN Stem Cell QC Research Associate B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
Performing routine quality control testing of stem cell products using protocol-defined assays to demonstrate their activity. The assays include culturing and handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation and workflow is required. Other duties include instrumentation maintenance, reagent preparation and routine lab support for QC antibody testing using western blot, simple wes and immunohistochemistry. | 07/28/2021 |
| 8246 | ProteinSimple [Bio-Techne] Wallingford, CT Research Associate Assay Development Master’s degree in Chemistry, Biology, or equivalent. Exp: 0 to 2 years |
An exciting opportunity to join a rapidly growing Bio Technology company. Work with a team of scientists to develop high quality immunoassay products for the Simple Plex department. As part of the Simple Plex Assay Development team you will be working towards creating novel commercial immunoassays, optimization of components, developing manufacturing procedures, and performing necessary troubleshooting. The team you will join is fresh, passionate and energetic, and you will have the collaborative support from experienced leadership and a helpful team. | 07/28/2021 |
| 8247 | PTC Therapeutics South Plainfield, NJ BS-MS Molecular Biologist Master’s degree in a scientific discipline. Exp: 0-2 years |
The BS-MS Molecular Biologist is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. The BS-MS Molecular Biologist supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. | 07/29/2021 |
| 8248 | PTC Therapeutics South Plainfield, NJ Contract, Biology Master’s degree in a scientific discipline. Exp: 0- 2 years |
The Contract, Biology is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. The Contract, Biology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. | 07/29/2021 |
| 8249 | PTC Therapeutics Pennington, NJ Associate Scientist, Quality Control (GMP Testing) - Gene Therapy Master’s degree in biology, molecular biology, virology, biochemistry or related discipline. Exp: 1 year |
In this newly created role, the Associate Scientist, Quality Control (GMP Testing) - Gene Therapy is responsible for the execution and analysis of compendial assays such as Appearance, pH, Osmolality, Subvisible Particles, and Conductivity to support drug substance/drug product release and stability testing for the gene therapy Technical Operation organization. Testing responsibility may also include well-established bioanalytical assays such as SDS-PAGE, CE-SDS, BCA and HPLC-SEC. S/He is also responsible for communicating assay results to his/her supervisor. The incumbent works cross-functionally with internal departments and external resources on Quality Control and GMP testing-related issues. The Associate Scientist, Quality Control (GMP Testing) – Gene Therapy supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. | 07/29/2021 |
| 8250 | Proteintech Rosemont, IL Scientist I; Bioconjugation A bachelor’s degree in an appropriate area of specialization (Molecular Biology, Cell Biology, Biochemistry, or related life sciences). Exp: New grads |
New grads with lab experience are encouraged to apply. The successful candidate will support the development and optimization of processes in bioconjugation of antibodies for use in various applications like Flow Cytometry and IHC. | 07/29/2021 |
| 8251 | Proteintech Rosemont, IL Scientist I; Cell Biology Bachelor’s degree in an appropriate area of specialization (molecular biology, Cell Biology, biochemistry, or related life sciences). Exp: New grads |
New grads with lab experience are encouraged to apply. The successful candidate will support the development and optimization of processes that produce cytokines and growth factors. These proteins will be used in cell therapy and stem cell research. | 07/29/2021 |
| 8252 | QPS Newark, DE BA - Associate Scientist I Bachelor’s degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline. Exp: trainee |
As an Associate Scientist in our Bioanalytical department, you will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. | 07/29/2021 |
| 8253 | QPS Newark, DE BA - Associate Scientist II Bachelor’s degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline. Exp: trainee |
As an Associate Scientist in our Bioanalytical department, you will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. | 07/29/2021 |
| 8254 | Quidel Carlsbad, CA Associate Process Group Chemist B.S./B.A. Life/Applied Sciences or equivalent experience. Exp: 6 months |
The Associate Process Group Chemist, in accordance with forecasted requirements, participates in the manufacture of products within QSR and ISO regulations. This position reviews and reconciles documents and work orders, supports assigned projects with supervision, participates in product transfers, supports departmental troubleshooting and process improvement teams, and displays an improving working knowledge of business processes as they relate to manufacturing. | 07/29/2021 |
| 8255 | Quidel San Diego, CA Bioengineer Master’s degree in biochemistry, chemistry, physics, bioengineering, related field. Exp: 1 year |
Quidel is looking for a Bioengineer to join our team in the Mira Mesa area of San Diego. The Bioengineer provides technical expertise to the design and development of new and novel medical device product(s). Designs and implements new methodologies, materials, machines, processes, or products. Develops new concepts from initial design to market release. Conducts feasibility, development, verification and validation studies of the design to determine the product’s ability to function as intended. Maintains detailed documentation throughout all phases of research and development. Coordinates activities with outside suppliers and consultants to ensure the delivery of supplies or services needed to meet scheduled timelines. | 07/29/2021 |
| 8256 | Quotient Sciences Boothwyn, PA Lab Assistant Bachelor's degree preferred. Exp: 0-3 years |
The position supports any one of the functional areas and carries out the responsibility under full supervision. | 07/29/2021 |
| 8257 | Quotient Sciences Boothwyn, PA Commercial Analytical Scientist I B.S. in Chemistry or equivalent. Exp: 0-3 years |
The position may reside in any one of the functional areas and carry out the responsibility under supervision: Analytical method development, validation, and transfer activities. Formulation development work including Material characterization and physical testing API/raw material sampling and testing, In-process and finished product testing, cleaning verification swabbing and testing. Notebook/report review, training, technical writing activities. Implementing, testing, using, or administrating LIMS. To comply & adhere to Good Manufacturing Practice (GMP) standards. | 07/29/2021 |
| 8258 | Reaction Biology Malvern, PA Research Associate I – Biochemical Assays Bachelor’s Degree or equivalent in biochemistry or related discipline. Exp: 0-3 years |
We are looking for a reliable and motivated individual with a strong science background to work in our lab. The position is a bench position with the primary duty of executing a variety of enzymatic assays. | 07/29/2021 |
| 8259 | Roche Seattle, WA Research Associate I – SBX Biochemistry BS in Bioengineering, Biochemistry, Biology or related field. Exp: 0-2 years |
The Biochemistry SBX Workflow team is passionate and dedicated to our SBX™ technology and the impact high throughput, low-cost DNA sequencing will have on patient outcomes. We are looking for individuals who share this passion and are excited to join a dynamic, cross-functional and collaborative group. The right candidate will be self-driven and highly motivated to quickly learn new skills and techniques in order to help advance rapidly evolving projects. An interest in projects that bridge biology/biochemistry and engineering is a plus. This position is a great opportunity for growth and advancement within the team. | 07/30/2021 |
| 8260 | Salix Pharmaceuticals Rochester, NY Chemist I (5307) BS in Chemistry, or related field. Exp: 1-3 years |
Key technical position in our quality organization responsible for monitoring product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 07/30/2021 |
| 8261 | SalubrisBio Gaithersburg, MD Associate Scientist/Scientist – Analytical /Formulation Development BS, MS or Ph.D. in Biochemistry, Biophysics, Chemical Engineering, Biology, or other relevant scienti?c ?eld. Exp: 0-5 years |
Act as a key expert in analytical and/or formulation development and/or product characterization for monoclonal antibodies (mAbs) and antibody drug conjugates (ADCs). Carry out tests including, but not limited to, HPLC (RP, IEC, and HIC), CE-SDS, cIEF, DLS, SLS, MFI, glycan, peptide mapping and intact mass LC-MS, etc. Compile scientific data, perform data analysis and interpretation, prepare technical reports, and present scientific data at project team meeting. Develop, qualify, and transfer analytical methods, prepare SOPs and assay development reports, and provide troubleshooting as needed. Identify, design, execute, and evaluate formulations for drug substance (DS) and drug product (DP) through thermo, conformational, and photo stability and solubility studies. Collaborate and coordinate with colleagues in cell line, upstream, and downstream process development group. Ensure adherence to GMP compliance as applicable. Support drafting and review of regulatory filings and technical documents. | 07/30/2021 |
| 8262 | SalubrisBio Gaithersburg, MD Associate Scientist/Scientist/Senior Scientist-Upstream and Cell Line Development MS degree in biological sciences or related scientific fields. Exp: 0-3 years |
Perform culture of mammalian cells in plates (96-well, 24-well, 6-well and deep well), flasks (T and shaker), and small-scale bioreactors with aseptic technique. Perform transfection, selection, and single cell cloning of mammalian cells. Prepare Medium/reagents, equipment maintenance, and order supplies. Write and review standard operating procedures and technical reports. Maintain complete documentation records (including lab note books and electro data files) to support regulatory filings. | 07/30/2021 |
| 8263 | SalubrisBio Gaithersburg, MD Associate Scientist/Scientist-Downstream Process Development MS in Biochemical/Chemical Engineering, or related scientific disciplines. Exp: 1+ years |
Develop robust and scalable downstream processes at laboratory scale for the purification of antibodies or antibody-based therapeutic proteins with chromatography (affinity, IEX and/or HIC, etc.). Support scale-up of downstream processes and technology transfer to cGMP manufacturing facilities for clinical material production; work with cGMP manufacturing team to generate and review SOPs and batch record for traceability. Perform routine bench-work under limited supervision, effectively prioritize responsibilities and complete assignments in a timely manner. Able to analyze, interpret, and present results to project teams and write technical reports. Support equipment maintenance and calibration Train others as appropriate. | 07/30/2021 |
| 8264 | SAMDI Tech Chicago, IL Research Assistant B.S. in biology, biochemistry, chemistry, or related field. Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. Responsibilities include: Support preparation of reagents and materials for running biochemical assays. Assist in executing biochemical assays utilizing state of the art mass spectrometry Integrate automated liquid handling and support compound management Provide support for fundamental laboratory functions | 07/30/2021 |
| 8265 | SAMDI Tech Chicago, IL Research Assistant: Cell-Based Assays Bachelor’s degree in chemistry, biology, biochemistry, immunology, materials science, or related field. Exp: 1-3 years |
The Research Assistant will participate in cell-based research that assist our partners and collaborators with their drug discovery projects. The Research Assistant will also manage laboratory reagents and materials to ensure smooth operations and timely delivery of data to clients. The Research Assistant will report to the Associate Director of Cell-Based Assays. Responsibilities include: Maintain the accuracy of the cell line database and reagents inventory Routinely prepare reagents and experimental samples for cell-based assays Adhere to Standard Operating Procedures (SOPs) for general mammalian cell culture including growing, maintaining, expanding, freezing and thawing cell lines Liaise with study managers to provide quality service to clients, including creating client specific SOPs, collecting and analyzing data Assist in organizing and managing the laboratory including preventive maintenance of equipment to ensure a contaminant free environment Perform other related work as needed | 07/30/2021 |
| 8266 | Sanarus San Diego, CA Research Associate 2 M.S. Molecular Biology, Chemistry, Biochemistry or related field. Exp: 1 year |
Performs moderately complex experiments with input from supervisor. Understands experimental goal and exhibits critical thinking skills when evaluating data. Able to summarize related groups of experiments. Provides input to the experimental design. Analyze experimental data with minimal input from supervisor. Interprets experimental results in context of overall experimental goal. May provide input to follow up experiment designs May present data in group meetings. Collaborates and communicates effectively with peers and supervisors. Draft protocols and reports for verification and validation studies. Experience with molecular biology techniques including nucleic acid extractions, PCR and sequencing is highly desirable | 07/30/2021 |
| 8267 | Sanarus San Diego, CA Microbiology Research Associate 2 or 3 Bachelor of Science degree. Exp: 1-3 years |
The Microbiology Research Associate 2/3 will perform basic and advanced culture techniques, including microbiology, tissue culture and virus culture in support of assay development activities as well as product support activities. This includes sterile aerobic as well as anaerobic work technique and involves handling of infectious materials. In addition, the candidate will be required to perform molecular experiments, including PCR, sequencing and DNA/RNA extractions. | 07/30/2021 |
| 8268 | Sangamo Therapeutics Richmond, CA Temporary Research Associate I B.S. or higher in biology, virology, biochemistry, process engineering or related field. Exp: 1- 3+ years |
Sangamo Therapeutics is seeking a talented temporary development associate work in our Vector Production and Development Group. Tasks would include viral vector production using mammalian tissue culture cells and vector purification by ultracentrifugation or column chromatography. Maintenance of our production and inventory database is also required. Analysis of the viral vectors by qPCR and gels may also be performed. The position requires adaptability, excellent planning and communication skills as well as the ability to work in a fast-paced, team-oriented, multidisciplinary environment. | 07/30/2021 |
| 8269 | Sangamo Therapeutics Richmond, CA Temporary Research Associate I/II B.S. or higher in biology, virology, biochemistry, process engineering or related field. Exp: 1+ years |
Sangamo Therapeutics is seeking a talented temporary research associate to fill an open temporary position in our Vector Production and Development Group, manufacturing lentivirus in support of our research and preclinical efforts. | 07/30/2021 |
| 8270 | Sanofi Pasteur Framingham, MA Associate Scientist BS, MS Biotechnology Chemical Engineering, Biology, Biochemistry or relevant field. Exp: BS 0-3 years; MS 0-2 years |
The Downstream Purification Scientist position is part of Process Science Laboratory Group in Manufacturing Science & Technology (MSAT). The Process Science Laboratory group within MSAT is responsible for providing laboratory based technical support to Sanofi manufacturing facilities world wide. The main objectives are to drive next generation process development and support key strategic initiatives (such as Facility of Future) and lead Tech transfer, scale-up development and adaptation, control strategy implementation, process validation, comparability for Specialty Care biologics introduction at Sanofi and external Industrial sites. | 07/30/2021 |
| 8271 | Sanofi Pasteur Framingham, MA Quality Control Analyst I Bachelor's Degree in Life Sciences discipline. Exp: 1 Year |
This Quality Control Analyst I is responsible for performing routine testing of in-process samples, stability samples and final products in accordance with SOPs for product release. | 07/30/2021 |
| 8272 | Sarepta Therapeutics Andover, MA QC Associate, Gene Therapy Potency B.S. degree in molecular biology, cell biology or virology. Exp: 0- 1 year |
This individual will support quality control laboratory activities conducted at Sarepta Andover facility in the field of AAV therapeutic release and stability. The individual will assist in conducting release testing using state of art in vivo and in vitro potency assays. The position requires a background in cell culture, sample preparation and protein analysis. The work involves performing assays in a BSL-2 environment. The individual will work under the directions of a subject matter expert conducting experiments, reviewing release and stability data, writing technical reports, supporting analytical method validation and qualification activities. The individual will also assist in managing quality events (OOS, OOT, Deviation, Change Control, etc.) and data trending. All aspects of this position involves working in a GMP compliant manner. | 07/30/2021 |
| 8273 | Sarepta Therapeutics Dublin, OH Research Associate I, Gene Therapy R&D B.S. degree in Biology or related field. Exp: 1-3 years |
The Research Associate I provides laboratory support of day-to-day GCP/GLP analysis related to gene therapy drug development. The RAI assists in implementing and developing new laboratory techniques to support preclinical decision making. This role requires laboratory expertise/training in small animal handling and an understanding of various molecular biology assays. | 07/30/2021 |
| 8274 | Nanosyn Santa Rosa, CA Research Scientist II - Analytical Chemistry Advanced degree in chemistry. Exp: 0-2 years |
To ensure availability of appropriate and accurate analytical methods and providing testing for small molecule pharmaceuticals. | 7/20/2021 |
| 8275 | Nanosyn Santa Rosa, CA Associate Research Scientist B.S. in Chemistry, Biochemistry or other relevant discipline. Exp: 0-2 years |
Develop new methods for the synthesis of organic molecules and prepare intermediates for the synthesis of these molecules. Apply modern techniques of organic synthesis including a variety of organic reactions at several scales, inert atmosphere techniques, thin-layer chromatography, NMR, LC-MS, HPLC, MS, flash chromatography, recrystallization, distillation, etc. | 7/20/2021 |
| 8276 | Natera Austin, TX Clinical Laboratory Operator I BS/BA (or equivalent) in a biological science or a related field. Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. | 7/20/2021 |
| 8277 | Natera San Carlos, CA Clinical Laboratory Associate I BS/BA (or equivalent) in a biological science or similar field of study. Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate I to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. | 07/20/2021 |
| 8278 | Natera San Carlos, CA Research Associate 2 BS/BA in a biological science or equivalent. Exp: 1 year |
As a Research Associate II, you will be part of a high performance, cross-disciplinary team developing new molecular and genetic based tests. You will design studies under guidance and be hands on in the lab to execute experiments to support product development, verification, and validation. | 07/20/2021 |
| 8279 | Natera San Carlos, CA Research Technician BS or BA in related scientific discipline. Exp: 1 year |
You will work primarily with the R&D Scientific Operations team. Responsible for plasma and buffy coat isolation from whole blood, and importing sample data to LIMS. Responsible for sample processing activities including DNA extractions, DNA qualification and quantification (Bioanalyzer, QuBit, and Quant-It), RT-PCR. Maintenance of multiple mammalian cell lines utilizing aseptic techniques. Interacting with researchers to ensure timely delivery of cells and assay plates. Banking of cell lines in LN2, requiring some heavy lifting of storage racks. Recognize and escalate equipment and instrument malfunctions to appropriate personnel. Adhere to all standard operating procedures (SOP). Adhere to environmental, health and safety (EHS) guidelines and good clinical and laboratory practices (GCP/GLP) Performing practical laboratory work, scheduling day to day tasks, and ensuring timely delivery of quality results. Perform other tasks as specified by the manager/director | 07/20/2021 |
| 8280 | Nephron Pharmaceuticals West Columbia, SC Junior Engineer BS degree in Mechanical, Electrical, or Mechatronics Engineering preferred. Exp: 0-3 years |
Responsible for assigned Engineering projects. Participates in projects from the conceptual phase to production. Supports production operations with technical assistance and troubleshooting insight. Performs other Engineering duties as assigned or apparent. | 07/20/2021 |
| 8281 | Nephron Pharmaceuticals West Columbia, SC Microbiology Data Analyst Bachelor’s degree preferred. Exp: 1-2 years |
Provides data analysis, tracking and trending, and updates for the Environmental Monitoring (EM) program and product release through use of MODA, Power BI, and LabVantage systems. Creates and executes project work plans and revisions as appropriate to meet changing needs and requirements. Performs other job duties as assigned. | 07/20/2021 |
| 8282 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Weekend Shift (Fri.-Sun. - 7:00am to 7:00pm & Mon. - 8:00am to 12:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
Support quality control testing and research and development activities as needed. - Assists with additional work duties or responsibilities as evident or required. -Performs other duties as assigned or apparent -Relies on instructions and pre-established guidelines to perform job functions. -Works under immediate supervision. | 07/20/2021 |
| 8283 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Second Shift (Sun. - Thurs. - 2:00pm to 11:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
Support quality control testing and research and development activities as needed. - Assists with additional work duties or responsibilities as evident or required. -Performs other duties as assigned or apparent -Relies on instructions and pre-established guidelines to perform job functions. -Works under immediate supervision. | 07/20/2021 |
| 8284 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - First Shift (Mon. - Fri. - 8:00am to 5:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
Support quality control testing and research and development activities as needed. - Assists with additional work duties or responsibilities as evident or required. -Performs other duties as assigned or apparent -Relies on instructions and pre-established guidelines to perform job functions. -Works under immediate supervision. | 07/20/2021 |
| 8285 | Nexus Pharmaceuticals Lincolnshire, IL Analytical Chemist I BS or MS in Chemistry or related discipline. Exp: 0-1 years |
You will play a critical role as a part of the R&D team and will be responsible for the analytical testing and development of Nexus’s Injectable ANDA’s. Analytical testing may include instrumental analyses such as HPLC, GC, IC, UV-Vis as well as wet chemistry. You will develop and validate new analytical methods, analyze lab stability samples and perform analytical testing to support product development and regulatory submissions. | 07/21/2021 |
| 8286 | NGM Biopharmaceuticals South San Francisco, CA Research Associate, Immune Oncology Bachelor’s degree in a Biological Science. Exp: 1 year |
NGM is excited to hire an organized and highly motivated Research Associate to join our team, focused on supporting our immune oncology research and development efforts. This role is perfect for a recent college graduate who has previous lab experience with in vivo disease models, looking to apply their skills directly toward the development of cancer therapeutics. | 07/21/2021 |
| 8287 | Nova Biomedical Waltham, MA Quality Engineer I Undergraduate Degree in Science, Engineering, or related field. Exp: 0-2+ years |
As a Quality Engineer, you will be responsible for providing expertise and general oversight to the management and improvement of our company’s quality systems, creation of quality plans, document controls, change management, process controls, quality records, corrective and preventive activities, validations, risk assessments, and data management. Please note, this position will be fully onsite at our Waltham facility. | 07/21/2021 |
| 8288 | Novavax Gaithersburg, MD Research Associate I/II, Vaccine Development B.S. or M.S. in Biochemistry, Molecular Biology, Biology, Biomedical Engineering or related field. Exp: 0-2 years |
Support protein purification efforts through buffer preparation, SDS-PAGE, and Western blots. Perform ELISAs, PCRs, DNA isolation, DNA electrophoresis and other assays. Maintain cell lines using aseptic technique. Keep accurate documentation and analyze data with appropriate software. General lab organization including equipment maintenance and calibration, and inventory management of assay materials and reagents. Ability to work independently with minimal supervision. | 07/21/2021 |
| 8289 | Novavax Gaithersburg, MD Research Associate I - Clinical Immunology BS degree in relevant scientific discipline. Exp: 0-2 years |
We are seeking Research Associate I to join our Clinical Immunology department in Gaithersburg, MD. This individual will play an important role testing clinical samples. Qualified individuals are expected to generate accurate high throughput clinical data. | 07/21/2021 |
| 8290 | Novavax Gaithersburg, MD Research Associate I, Formulation Development MS degree in Bio/Chem Engineering, Biology, Chemistry, Pharmaceutical Science, Biochemistry, biophysics, Molecular Biology, Life Sciences, vaccine dev Exp: 0-2 years |
We are seeking to fill the Research Associate role of the Formulation Development department. This position will be a laboratory-based with tremendous learning potential in the area of drug formulation development. The Research Associate will report to the Formulation Development Team Lead Senior Scientist into the Process Development Department and work in a cross-functional team environment. | 07/21/2021 |
| 8291 | Novavax Gaithersburg, MD Research Associate I/II, Preclinical Immunology B.S. or M.S. in Immunology, Biology, Biochemistry, Molecular Biology or related field. Exp: 1 years' |
We are seeking a highly self-motivated and well organized individual to serve as a Research Associate I / II with immunological assay background to join our preclinical immunology group. The successful candidate will be a hands-on contributor who performs appropriate immunological assays to evaluate various vaccine candidates. This position will be located at our Gaithersburg, MD facility and will report to the senior manager, preClinical Development. | 07/21/2021 |
| 8292 | Nucelis San Diego, CA Downstrream Process and Fermentation Engineer M.S. degree in Biochemical Engineering, Mechanical, Agriculture Engineering or related discipline. Exp: 1 year |
Nucelis LLC is a metabolic engineering company in San Diego, CA, focused on the use of gene editing tools to construct commercially useful strains of microorganisms, and develop optimized fermentation and chemical processes to maximize their commercial advantage. Nucelis is seeking a highly capable and experienced Downstream Process and Fermentation Engineer to join our team. | 07/22/2021 |
| 8293 | Nurix Therapeutics San Francsico, CA Research Associate/Senior RA, DNA Encoded Scientist, Library Discovery B.S. or M.S. in life sciences (ex. chemistry, biochemistry, biology) Exp: 0-5 years |
We are seeking a talented and highly motivated scientist to join our Library Discovery team and help us augment our DNA encoded library collection. DEL synthesis requires a hybrid of techniques that are borrowed from chemistry environments: chemical reaction setup, LCMS analysis, SAR evaluation, split and pool library synthesis workflows, parallel reaction development, as well as from biology laboratories: aqueous buffer preparation, centrifuge use, ethanol precipitation of DNA, A260 DNA quantification, gel electrophoresis, bioanalyzer analysis, enzymatic DNA ligation. An exposure to some of these techniques is helpful in training into a DNA encoded scientist. As a member of a dynamic multi-disciplinary project team, this person will collaborate with a broad group of scientists within Nurix as well as with external collaborators. | 07/22/2021 |
| 8294 | Nutix Therapeutics San Francsico, CA Research Associate, Analytical Chemistry – Purification B.S. or equivalent degree in chemistry, analytical chemistry, or related field. Exp: (0-3) years |
We are seeking a highly motivated individual with a 0-3 years of lab experience to join the small molecule purification group at Nurix. This position will perform purifications of small molecule libraries by mass directed HPLC, run routine purity checks and submit samples for analysis by NMR. The candidate requires the ability to work in a fast-paced laboratory setting using state of the art analytical and preparative equipment. This role also requires basic lab / chemical handling safety and the ability to lift 40 lbs. The candidate should have a strong desire to learn new techniques, stay up to date with purification trends, and an aptitude for robotic automation workflows. The ideal candidate will be self-driven, resourceful, organized, focused, and enjoy working in the dynamic team environment here at Nurix. Required Qualifications | 07/22/2021 |
| 8295 | Nutcracker Therapeutics Emeryville, CA Quality Control (QC) Specialist/ Research Associate Master’s degree in a relevant field, e.g., Chemistry, Biology, Biochemistry, Molecular Biology, Bioengineering. Exp: 1-year |
We are looking for a talented and hands-on Senior Quality Control Analyst to be a pivotal contributor to bringing up cGMP laboratory operations, validating analytical methods, and supporting our analytical and process development projects. This individual will enjoy high-quality data in the laboratory and implementing streamlined processes to ensure compliant cGMP guidelines. Expertise with a variety of analytical methods considered, including LC, LC-MS, GC, CE, ELISA, bioassay, q or ddPCR, NGS sequencing, microbial control or impurities testing. cGMP experience is a plus | 07/22/2021 |
| 8296 | Ocular Therapeutix Bedford, MA Process Development Engineer I Bachelor’s degree (MS desirable) in Chemical Engineering, Biomedical Engineering, Chemistry, or related discipline. Exp: 0-2 years |
The Process Development Engineer I will execute development activities for hydrogel-based drug product candidates in pre-clinical stage innovation projects. The role includes but is not limited to formulation design and execution, process development and optimization, and drug product manufacturing to support external collaboration partnerships and internal projects. This individual will assist in the execution of assigned project activities and work with project team members to develop and manufacture the drug products. They may assist in overseeing the execution of project tasks and monitor the activities and deliverables of project aspects in a leadership role. The position is set in a dynamic and fast-paced environment. Critical areas of focus will be assisting with formulation design, research material production, process scale up and optimization, and new process development. Ability to leverage various project teams at Ocular will be a key ability of this individual. | 07/23/2021 |
| 8297 | Olympus San Jose, CA Engineer I Bachelors Degree in Engineering. Exp: 1 year |
The Engineer I provides engineering support for introduction of new products and alternate repair activities. They function as Project Coordinator on more complicated projects as defined by the Manager by providing technical information to other project participants recommending cost effective procedures tracking and maintaining implementation dates and documenting completed projects. The successful candidate provides support to Associate Engineer on his/her assigned projects. | 07/23/2021 |
| 8298 | Olympus San Jose, CA Quality Assurance Engineer I Bachelor's Degree in Engineering or Scientific Discipline (or equivalent). Exp: 0 to 2 years |
The Quality Assurance Engineer I is responsible for providing Quality Engineering input to support Production Operations and Engineering activities. Maintains and follows Quality Engineering methodologies systems and practices which meet Olympus customer and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, and communication on Quality initiatives to support departmental functional site divisional and corporate Quality goals and priorities. When needed works with Olympus Tokyo representatives liaisons to resolve Quality related issues. | 07/23/2021 |
| 8299 | Omeros Seattle, WA Research Associate I, Biochemistry Requires a BS degree. Exp: 0 - 2 years |
Performing a variety of routine and non-routine research assignments as supervised by a Ph.D. scientist Conducting routine molecular biology bench work (e.g. primer design and site-directed mutagenesis, plasmid DNA purification, sequencing) Performing routine eukaryotic cell culture work (e.g. cell passaging, viability determination and transient transfection) Purifying recombinant proteins using standard chromatographic techniques (e.g. affinity chromatography, size-exclusion chromatography) Characterizing protein purity and quality using standard biochemical techniques (e.g. SDS-PAGE, Western blotting, thermal shift assays) Maintaining a detailed and up-to-date electronic lab notebook Analyzing and summarizing data, presenting at internal meetings, and communicating regularly with managers and coworkers on experiment progress Managing laboratory equipment and consumables | 07/23/2021 |
| 8300 | OncoMyx Therapeutics Phoenix, AZ Research Assistant/Associate Bachelor’s degree (BS/BA) in a biomedical science or related discipline. Exp: 1-2 year |
OncoMyx is seeking a highly motivated and creative Research Assistant/Associate to join a group of researchers evaluating novel oncolytic virus therapies. The candidate will work within project teams to advance research stage programs into pre-clinical development, and provide in-vitro, in-vivo and ex-vivo data essential to drive projects into clinical development. | 07/23/2021 |
| 8301 | Ontera Santa Cruz, CA Research Associate Bachelor’s degree in Chemistry, Biochemistry, Biology, Bioengineering, or related field. Exp: Entry-level |
We are seeking a highly motivated Research Associate to join the Biochemistry Research and Development group at Ontera. The Research Associate position is responsible for conducting experiments in an effort to develop assays for deployment onto Ontera’s solid-state nanopore detection platform. The incumbent will perform established assays, as well as contribute to the development of new experimental tests. | 07/23/2021 |
| 8302 | Ontera Santa Cruz, CA Research Associate Bachelor’s degree in Chemistry, Biochemistry, Biology, Bioengineering or related field. Exp: Entry-level |
We are seeking a highly-motivated Research Associate to join the Nanopore Research and Development group at Ontera. The Research Associate position is responsible for the execution of a wide variety of testing on Ontera’s solid-state nanopores. The incumbent will perform established assays, as well as contribute to the development of new experimental tests. | 07/23/2021 |
| 8303 | Orna Therapeutics Cambridge, MA Research Associate - RNA Engineering BS in biology, genetics, biochemistry or related discipline. Exp: 0-4 years |
We are seeking an exceptional researcher to join our team as a Research Associate to refine our best-in-class proprietary RNA expression and delivery platform. The ideal candidate has at least a bachelor’s degree in a biology-related field with significant RNA experience. They will be able to quickly learn and integrate new protocols into existing workflows; possess strong oral and written communication capabilities; demonstrate excellent collaboration & interpersonal skills; and be adept at problem solving in a fast-paced environment. | 07/23/2021 |
| 8304 | Pacific Biosciences Menlo Park, CA Research Associate, Sample Prep Biochemistry B.S. degree in Biochemistry, Molecular Biology or related field. Exp: 1+ years |
Pacific Biosciences seeks a Research Assistant with a molecular biology background to join the Sample Preparation Team. The successful candidate will contribute to the development of the core front-end sample preparation products for the Pacific Biosciences SMRTTM (single molecule, real-time) sequencing platforms. The primary objectives of the team are to develop highly scalable, user-friendly, products and protocols that increase system throughput. Experience with molecular biology techniques such as genomic DNA extraction, PCR, industry-standard sample prep practices (NGS), and sequencing applications is essential. The successful candidate will be working in a fast-paced and energetic environment, interacting with scientists and engineers with diverse backgrounds. | 07/23/2021 |
| 8305 | Pacira Biosciences San Diego, CA Microbiologist 1 BS degree in Microbiology or other life science from an accredited college or university. Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products | 07/23/2021 |
| 8306 | PACT Pharma South San Francisco, CA Research Associate, Flow Cytometry Bachelor's Degree or a Master's Degree Exp: 1 + years |
We are currently recruiting for a Research Associate in the clinical pipeline group to continue advancing PACT Pharma's cutting-edge engineered cell product. This will be a unique opportunity to see your ideas rapidly translate into the clinic and impact patient lives. The person in this role will be responsible for the evaluation of T cells as part of the product selection process prior to the manufacturing of PACT Pharma's adoptive cell therapy product (neoTCR-P1) for clinical patients. This process is performed in a GMP-like laboratory setting and includes characterizing T cell phenotype and functionality using state-of-the-art flow cytometry-based methods and automation. The ideal candidate should enjoy operating in an exceptionally dynamic and cooperative environment. | 07/23/2021 |
| 8307 | Pall [Danaher] Westborough, MA Quality Engineer Bachelor’s Degree in Engineering discipline. Exp: 1-3 years |
The role of PASS Quality Engineer will support the quality management system of PASS Westborough by ensuring Pall Corporate, Customer, and Regulatory requirements are being met through project execution and delivery of product. This includes management of quality performance targets including customer complaints and nonconformance investigations, and supplier management. | 07/23/2021 |
| 8308 | Pall [Danaher] Duncan, SC QA Specialist (Batch) Bachelor’s degree in a scientific field, preferably in Life Sciences (Bio, Biomedical, Chemical, Pharma) or similar. Exp: 1-3 years |
The QA Specialist (Batch) works as part of Quality Assurance team and will mainly be responsible for the batch record review and final product release and certification. This person will also assist with the maintenance of quality data, creation of sample plans and other routine Quality Assurance tasks. | 07/23/2021 |
| 8309 | Par Pharmaceutical Rochester, MI Chemist II (Afternoon Shift) Master’s Degree in chemistry, chemical engineering or related field. Exp: 1+ years’ |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 07/23/2021 |
| 8310 | Par Pharmaceutical Rochester, MI Quality Associate Specialist, Product Release (Afternoon Shift) BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 07/23/2021 |
| 8311 | Parse Biosciences Seattle, WA Research Associate - Single Cell Genomics BA or BSc in molecular biology (or related field). Exp: one year |
As a research associate at Parse Biosciences, you will work at the cutting edge of molecular biology and genomics as part of a collaborative team. You will design and perform experiments to improve our existing single-cell RNA-sequencing kits as well as demonstrate new applications for our kits. You will also share responsibilities in organizing inventory, assembling kits, testing kits internally, reagent quality control, and maintaining the lab. You will interact with customers--both helping them with technical concerns and incorporating their feedback into the kit. | 07/23/2021 |
| 8312 | PBL Assay Science Piscataway, NJ Junior Life Science Product Support Specialist 4-year degree in life science-related major. Exp: 1+ year |
Provide focused support to troubleshoot, resolve, and track product-related issues. Assist in the preparation and organization of technical content to support marketing of product and service offerings. This position will also provide support for any marketing initiatives to further company goals. | 07/23/2021 |
| 8313 | Phanes Therapeutics San Diego, CA Assistant Scientist / Associate Scientist I (multiple positions) Completed BS/MS in chemistry, biology, chemical biology, biochemistry, biochemical/biomedical engineering, or related fields. Exp: 0-3 years |
We are looking for Assistant Scientists / Associate Scientists to join our discovery research teams. This position is intended for someone with a bachelor’s degree in biology/biochemistry or a related area and will work at our R&D site in San Diego, CA. He or she should have basic or intermediate training and knowledge in biochemistry, molecular biology, pharmacology or a related field. The candidate will have opportunities to learn and be trained in a laboratory to support a wide range of ongoing projects. Some understanding in molecular biology, biochemistry, cell culture, or purification of recombinant proteins is required. Laboratory experience is preferred. The candidate must be a team player and is expected to work with other scientific staff on discovery projects. This person must be willing to collaborate and communicate with other team members within the company. | 07/23/2021 |
| 8314 | Just Biotherapeutics Redmond, WA Associate Scientist, Drug Product Design BS in biochemistry, chemistry, biophysics, chemical engineering, or related fields. Exp: 0-3 years |
Just is seeking a motivated and creative researcher who desires a significant opportunity to improve worldwide access to biotherapeutics. This position is a hands-on, laboratory based role supporting all stages of formulation development from early stage formulation verification to late stage, commercial formulation design of antibodies, Fc-conjugates and other novel protein based molecules. The successful candidate will have experience working in an analytical laboratory setting and be familiar with chromatographic, electrophoretic, and spectroscopic techniques. Experience with high throughput, robotic techniques, statistical design of experiments, and data modeling is a plus. The candidate must possess a strong ability to work in a team while supporting multiple projects. Strong organizational, written, and verbal communication skills are necessary. The ideal candidate is efficient, curious, creative, enthusiastic, works well independently and in teams, and looks for ways to improve processes and technology. | 7/11/2021 |
| 8315 | Just Biotherapeutics Redmond, WA Associate Scientist, Functional Biocharacterization BS in Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering, Chemistry or related field . Exp: 0-5 years’ |
Just is seeking a motivated and creative Associate Scientist who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work with a multidisciplinary team for the analytical and functional biocharacterization of large molecule therapeutics and analysis of process impurities. Experience with ELISA binding assays, DNA extraction, and PCR preferred. Additional experience with cell-based and ligand-receptor binding assays, as well as high-throughput methods and liquid handling robotics beneficial. The successful candidate has strong written and verbal communication skills and is interested in ways to improve technology. The ability to multitask and to work both independently and in teams in a fast-paced collaborative environment is necessary. | 7/11/2021 |
| 8316 | Just Biotherapeutics Seattle, WA Associate Scientist, Functional Biocharacterization BS in Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering, Chemistry or related field. Exp: 0-5 years’ |
Just is seeking a motivated and creative Associate Scientist who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work with a multidisciplinary team for the analytical and functional biocharacterization of large molecule therapeutics and analysis of process impurities. Experience with ELISA binding assays, DNA extraction, and PCR preferred. Additional experience with cell-based and ligand-receptor binding assays, as well as high-throughput methods and liquid handling robotics beneficial. The successful candidate has strong written and verbal communication skills and is interested in ways to improve technology. The ability to multitask and to work both independently and in teams in a fast-paced collaborative environment is necessary. | 7/11/2021 |
| 8317 | Just Biotherapeutics Redmond, WA Associate Scientist, Protein Expression BS. Exp: 0-5 years’ |
Just is seeking a motivated and creative researcher who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work as a member of a small but highly experienced and innovative team to develop cell lines for the purpose of manufacturing biologic therapeutics. The successful candidate will have experience with cell culture as well as a strong foundation in cell and molecular biology. Experience in cell line development, cell culture automation, and expression vector design, is a plus. The candidate must possess strong written and verbal communication skills, strong organizational skills, a desire to learn new scientific concepts, and an ability to work directly with scientific staff across multiple disciplines. | 07/11/2021 |
| 8318 | Just Biotherapeutics Redmond, WA Materials Process Engineer I/II - Manufacturing Technical Operations Bachelor’s degree in engineering science or related program. Exp: 1-3 years |
Just is seeking a highly motivated Materials Engineer in the Manufacturing Technical Operations group that desires a significant opportunity to improve worldwide access to biotherapeutics. The primary focus of this job is to work with operations to develop, procure, commission and test single use assemblies and manifolds for our flexible manufacturing facilities. Candidate will coordinate with supply groups to bring components into the facility and with the Quality group to develop operating procedures and specifications for the materials. In addition, the candidate will be responsible for supporting the evaluation and introduction of new single use manufacturing technologies, including assessments of leachables and extractables, and assisting with the commissioning and validation of new process equipment in the facility. | 07/11/2021 |
| 8319 | KBI Biopharma Boulder, CO Research Associate/Sr. Research Associate B.A. or B.S. degree in Chemical Engineering, Chemistry, Biochemistry or related field. Exp: Open |
KBI's Particle Characterization Core is looking for an engineer/scientist to become our next colleague and learn the fine art of particle characterization. Our new associate will have an active role in a dynamic laboratory environment that will include learning cutting-edge analytical techniques, development of data analysis tools, establishing direct relationships with clients, and continuing to build a world-class specialty analytical business. If you are eager to learn and want to jump start a career in pharmaceutical analytics, you might be the person we are looking for! | 07/11/2021 |
| 8320 | Kite Pharma Emeryville, CA Research Associate, Cell Biology – Protein Expression BS or MS degree in Cell Biology or related fields. Exp: 1+ years |
We are seeking a highly motivated Research Associate to join Kite’s research team at our Emeryville, CA, location. Specifically, you will be part of the Protein Sciences team, supporting our early pipeline through generation and characterization of critical recombinant protein tools. You will work in a collaborative cross-functional team environment as you support our on-site protein production capability. | 07/11/2021 |
| 8321 | Kite Pharma Santa Monica, CA Senior Research Associate I, Cell Biology - Automation Master of Science Degree Exp: 1+ years |
We are seeking a highly motivated individual to join us as a Senior Research Associate in our Automation core group. You will play a key role in advancing our CAR pipeline and contributing to develop next generation cell therapies as you support our efforts in this exciting new area of cancer immunotherapy. The successful candidate will be expected to perform experiments, organize and analyze results, and communicate findings in team meetings. This will be a hands-on role supporting pipeline activities. | 07/11/2021 |
| 8322 | Korro Bio Cambridge, MA Research Associate, Oligonucleotide Compound Management Bachelor’s degree Exp: 0-2 years |
Korro Bio is seeking a passionate, driven, and creative entry-level scientist to join our oligonucleotide discovery chemistry team and work with an enthusiastic team of highly skilled scientists in a dynamic, growing company. The successful candidate will be responsible for oligonucleotide analysis and independently assist in tracking, receipt, handling, organization, sample preparation, storage and distribution of oligonucleotide compounds and work closely with cross functional team to advance our RNA editing drug discovery programs. The candidate will also be responsible for quantifying, performing purity analysis via HPLC/LCMS, and documenting results. Additional responsibilities include maintaining an active inventory of compounds, both physical and virtual. Candidate must express a high attention to detail, be comfortable multitasking and ability to function in an interdisciplinary and fast-paced startup environment. | 07/11/2021 |
| 8323 | Lantheus Medical Imaging N. Billerica, MA Process Engineer I Bachelor’s Degree in Engineering or related science oriented discipline. Exp: 1 to 2 years |
An ideal candidate would be familiar with validation and parenteral products. Have strong technical skills in problem solving and aseptic manufacturing processes. Be able to use project management skills to lead cross functional teams through data based decision making for technical transfers or project improvements. Support larger projects collaborating across multiple teams. Strong partnership skills to build and maintain relationships. Be able to handle varied tasks supporting group projects and routine manufacturing. | 07/11/2021 |
| 8324 | Lipocine Salt Lake City, UT Product Development, Associate Scientist BS/MS in chemistry/analytical chemistry/pharmaceutical sciences/ related scientific field. Exp: 1-3 years |
Under minimal/no supervision develop and validate analytical methods to support product development, release testing and stability activities for pharmaceutical drug product programs. Perform physical and chemical tests on active pharmaceutical ingredients, raw materials, in-process, and finished products using various wet chemical, physical and instrumental techniques. Hands on experience with HPLC/UPLC with various detectors, related spectroscopy, KF (Karl Fisher), dissolution, and other common analytical methods. Conduct laboratory experiments in support of formulation and process development. Assist/perform manufacturing preclinical formulations and early clinical supplies. Generate and collate the data, perform required calculations and document experiments and results in a laboratory notebook following GMP/GLP practices. Critically assess experimental data and provide interpretation of results. Author SOPs, technical reports such as method development/validation, formulation report and other relevant scientific information packages for internal use or agency submissions. Prepare drug product stability protocols and reports. Evaluate the stability data and trends. Ensure the cleanliness, calibration and maintenance of laboratory equipment/stability chambers and work areas to ensure compliance with SOPs, GLPs and cGMPs. | 07/13/2021 |
| 8325 | LogicBio Therapeutics Lexington, MA Research Associate/Senior Research Associate Gene Therapy Bachelor’s degree in Biology, Biochemistry or a related field. Exp: 1- 3 years |
LogicBio is seeking a highly motivated team member who will assist the team with the in vitro and in vivo assays related to developing gene therapy products. Specifically, the successful candidate will be involved in maintenance, expansion and banking of cell culture lines, in vitro and in vivo analytical and functional bioassays for characterizing internal and external AAV vector product, molecular quantification assays, potency assessment and biodistribution studies. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in an efficient, highly interactive, goal-oriented team environment, and working with minimal supervision. | 07/13/2021 |
| 8326 | LogicBio Therapeutics Lexington, MA Research Associate/Senior Research Associate in Preclinical and Translational Biomarkers Bachelor’s or Master’s degree in biological sciences such as biochemistry, molecular biology, biotechnology, or related science discipline. Exp: 1-4 years |
LogicBio is seeking to grow our functional Preclinical and Translational Biomarker team. This is a unique opportunity to join an innovative biotech and apply cutting edge techniques to enable drug discovery and development. If you share our passion and sense of urgency for finding a lasting cure for patients, and are looking for a dynamic, collaborative and fulfilling work environment, we invite you to join our team. | 07/13/2021 |
| 8327 | Loop Genomics San Jose, CA Service Research Associate B.Sc or M.Sc. Exp: 1-2 years |
We are looking for an outstanding team player to join our NGS sample prep team and report to the Director of Molecular Biology. The individual will provide next generation sequencing service to our customers that incorporates Loop Genomics's long read technology with Illumina's short read sequencing platforms. This includes applying the standard operating procedure during NGS library preparation, as well as custom solutions tailored to the specific sequencing projects. The individual will also assist in testing and improving the robustness of Loop Genomics’s library preparation kits. This role requires excellent laboratory liquid handling skills and consistent performance of various wet lab operations. The ideal candidate is a dedicated and detail-oriented individual who thrives in a fast-paced work environment, has a solid background in molecular biology techniques, and shares our passion in bringing technology to change the current paradigm of DNA sequencing. | 07/13/2021 |
| 8328 | Lucigen Charleston, SC QC Chemist (23827) Bachelor of Science degree or equivalent. Exp: one-year |
This is an entry QC chemist position where one is responsible to make check standards, routine instrument maintenance and operation of GC/MS, GC/FID, HPLC, and UHPLC/MS, validating manufactured products in a timely manner. Attention to detail, teamwork, the ability to thrive in a fast-paced work environment and organizational skills are necessary to excel in this position. | 07/14/2021 |
| 8329 | Lucigen Petaluma, CA PD Chemist (23424) BS/MS in Chemistry, Chemical Engineering or related discipline. Exp: 1 year |
We are looking for highly a motivated chemist, biochemist and/or chemical engineer to join in our newly commissioned state-of-art therapeutic oligonucleotide GMP manufacturing facility in Petaluma, CA. This individual will work in a Process Development lab to support therapeutic oligonucleotide manufacturing process development, transfer and trouble-shooting production issues. | 07/14/2021 |
| 8330 | Lung Biotechnology La Jolla, CA Research Associate I - iPSC Bachelor’s degree in biology or related discipline. Preferred - Master’s degree in biology, cell biology, or related discipline. Exp: 1+ year |
The Research Associate I, Cell Biology (iPSC) will work in a cross-disciplinary R&D team, in collaboration with internal and external partners, focused on organ manufacturing. Responsible for generation, genome engineering and expansion of human-induced pluripotent stem cells for use in differentiation and cellularization of natural and synthetic scaffolds to create functional human organs. | 07/14/2021 |
| 8331 | Lung Biotechnology La Jolla, CA Research Associate I - Cell Biology Bachelor’s degree in biology or related discipline. Preferred - Master’s degree in biology, cell biology, or related discipline. Exp: 1+ years’ |
The Research Associate I, Cell Biology works in a cross-disciplinary R&D team, in collaboration with internal and external partners, focused on organ manufacturing. The successful candidate will be responsible for carrying out pilot and large-scale mammalian cell differentiation and expansion, as well as assay development and implementation for determining the function and quality of desired cell types for use in cellularization of natural and synthetic scaffolds to create functional human organs. | 07/14/2021 |
| 8332 | Magenta Therapeutics Cambridge, MA Research Associate/Senior Research Associate, In Vitro Biology BS in a relevant field (biology/immunology) Exp: 1 year's |
Magenta Therapeutics is a clinical-stage biotechnology company developing therapeutics to reset the immune system to cure more patients with devastating and life-threatening diseases. This immune reset approach can be applied through stem cell transplant to multiple diseases, including autoimmune diseases, such as multiple sclerosis and systemic sclerosis; blood cancers, such as acute myeloid leukemia; and genetic diseases, such as sickle cell disease. Magenta’s comprehensive approach to precision immune system reset will transform many aspects of the transplant process, aiming to make it safer and more effective. Our culture is fueled by a driven, passionate group of people committed to making a difference, seizing opportunities for maximum impact, and pursuing progress for the patients we seek to serve. We are seeking a highly motivated scientist to join our in vitro biology team. The successful candidate will be an integral member of a team involved in multiple projects at various stages of development, including the identification and validation of new targets and in vitro proof-of-concept studies. The position requires experience working with primary human cells, cell lines, and experience in assay development and optimization. | 07/15/2021 |
| 8333 | McGuff Pharmaceuticals Santa Ana, CA Quality and Validation Technician Bachelor’s degree (B.A./B.S.) of Science in Engineering, Chemistry or related field or equivalent is a plus. Exp: 1-2 years |
McGuff Pharmaceuticals, Inc. in Santa Ana, CA is looking for a Biopharmaceutical Quality/Validation Technician in Santa Ana, CA. The Quality/Validation Technician (QT) will work closely with the Quality Engineering and Validation Supervisor to plan, organize and perform commissioning, qualification and validation for defined processes, facilities, equipment and process controls that meet McGuff Pharmaceutical’s high standards. The Technician will maintain the existing manufacturing facility by maintaining the calibration program and periodic review/requalification program. The QVT will develop, plan, coordinate and execute qualification projects associated with drug product sterile contract manufacturing, aseptic processing, filling, and packaging. The Technician shall be familiar with the qualification of facilities, pharmaceutical manufacturing equipment/systems, sterilization processes, sterile filling processes, cleaning processes, environmental room monitoring, media fills, and process validation runs. The Technician will be capable of executing equipment IQ/OQ/PQ and process validations as required. In addition, the Technician will also assist, in a team based approach, the development and improvement of processes to ensure such processes meet McGuff Pharmaceutical’s high standards of process capability, reliability, and repeatability. The Technician will be capable of coordinating and executing process validations and associated system operational needs including, but not limited to, equipment and computer system Installation and Operation Qualifications (IQ/OQ) including temperature mapping, Performance Qualification (PQ) of Utilities, Sterilization and Decontamination Systems, Process Performance Qualification (PPQ), and full process validation documentation. Duties may also include assisting with and evaluating specification development, equipment procurement, operation and maintenance procedure development, and qualifying raw materials, in-process materials and finished goods, as required. The Technician shall ensure McGuff processes are compliant with cGMP requirements. | 07/15/2021 |
| 8334 | Medpace Cincinnati, OH Entry Level- Laboratory Technician Bachelor's degree. Exp: Entry level |
Prepare samples according to project protocol and/or related SOPs; Maintain compliant laboratory documentation; Perform data analysis and data checking; Interpret results obtained for accuracy and acceptability; Clean and sterilize laboratory equipment; and Other duties deemed necessary. | 07/15/2021 |
| 8335 | Medtronic Brooklyn Center, MN Electrical Test Engineer I Bachelors in Electrical Engineering, Controls Engineering, Industrial Engineering, Computer Engineering or similar Engineering discipline Exp: 0+ years |
The Electrical Test Engineer role designs, delivers, and supports equipment software solutions for a wide range of innovative medical electronics-based products and process control equipment. They are responsible for the development and release of Test equipment solutions supporting the release of new product manufacturing lines. This engineer would also be involved in determining if existing equipment software is adequate to support production manufacturing requirements for new products. This engineer would be responsible for designing and implementing the software and integrating the hardware portion of an equipment solution. This development is accomplished by interfacing with manufacturing and process development engineers to create a compliant solution for production equipment release and support. The equipment solution development includes debugging while interfacing to the equipment; perform R&R (repeatability & reproducibility) analyses; qualification and validation documentation, and support for system releases. Utilizes software environments including LabVIEW and TestStand. Troubleshoots software and hardware problems using root cause analysis and provides technical solutions for equipment-related problems and provides yield improvement solutions. | 07/15/2021 |
| 8336 | Medtronic Boulder, CO Electrical Engineer I Bachelor’s degree in Electronics or Electrical Engineering. Exp: 0+ years |
In this exciting role as a Sustaining Engineer you will have responsibility to work within the R&D Sustaining Engineering team, part of the Respiratory Interventions business group. The Sustaining Engineering group’s primary responsibilities are to support products currently on the market and the Stewardship of products following the transfer from development into commercialization. As a Sustaining Engineer you will be responsible for the planning and execution of product design related changes and remediation by leading cross-functional teams and managing project execution from initiation through completion within the framework of Medtronic’s Change Development Process (CDP). In addition to implementing design changes that enhance performance, address quality issues, and maintain compliance to applicable standards, the Sustaining Engineer performs product investigations, determines root cause, identifies and implements corrections and corrective actions. | 07/15/2021 |
| 8337 | Medtronic Boulder, CO Quality Engineer I Bachelors degree required. Exp: 0 years |
Functions will be performed under supervision in a biohazard lab handling medical devices Test and thoroughly evaluate used surgical devices to determine cause of failure Replicate reported failure mode with bench top or in vivo test methods and document observations accordingly Initiate and distribute Corrective Action Requests to Manufacturing or Engineering Departments as needed Prepare technical investigation reports based on results of evaluation and/or review of the manufacturing plant reports to be documented in the complaint database and incorporated into customer response letters Assist in the coordination of sanitization of clinically applied medical device returns and shipment to respective Medtronic Manufacturing facilities | 07/15/2021 |
| 8338 | Medtronic Santa Rosa, CA Manufacturing Equipment Engineer I Bachelor’s Degree in Mechanical Engineering. Exp: 0+ years |
The Manufacturing Equipment Engineer I is an hands-on engineering role and will work directly with a team of experienced engineers to assist in maintaining production equipment at their best performance. This will include design, development, and execution of various corrective and preventative activities across extrusion processes as well as troubleshooting process and equipment issues. Typical responsibilities revolve around fixture and tool design, process development, and equipment & process validation and corrective maintenance and trouble shooting in a regulated medical device environment. We are seeking motivated individuals who are interested in pursuing a career in complex mechanical engineering, electrical and pneumatic and plastics processes in extrusion technology for advance medical devices manufacturing at our Santa rosa, California location. The current project will be focused on a 3 year transfer project. | 07/15/2021 |
| 8339 | Medtronic Mounds View, MN Materials Engineer I Bachelors degree required in chemistry, material science, chemical engineering, polymer science, or related field. Exp: 0 years |
This position will support product and materials development for new and released product, ensuring product safety and reliability through the direction and execution of characterization testing. This will include providing problem solving, materials laboratory testing and data analysis in support of new and existing implantable biomedical devices and systems. Biocompatibility and biostability testing, as well as documenting product equivalence through appropriate characterization testing will also be included. You can grow your career with us; we hope you’ll consider joining our team! | 07/15/2021 |
| 8340 | Medtronic North Haven, CT Manufacturing Engineer I BS in Engineering Discipline - Mechanical, Industrial, and/or Biomedical Engineering. Exp: 0 years |
Medtronic's Surgical Solutions is seeking a Manufacturing Engineer for the Advanced Manufacturing Engineering team. The position will be in the New Product Development (NPD) Pilot Manufacturing team. The Engineer provides direct line support of products in Launch, Pilot and Commercialization phases. They perform troubleshooting of production equipment and tooling. Develop process improvements to decrease costs and scrap levels to ensure product delivery. They collaborate with their product NPD teams such as other AME, NPD Development and NPD Design Engineers. The Engineer will prioritize daily production activities, improvements, scheduling and production tracking. The Position is in a fast-paced, and collaborative environment that is supportive of program initiatives and compliant with the company’s best practices, Tenets and Philosophy. | 07/15/2021 |
| 8341 | Meissa Vaccines Redwood City, CA Quality Control Associate B.S. degree in science or a life science-related field of study. Exp: 1+ years |
Meissa Vaccines seeks a full-time Quality Control (QC) Associate or Sr. QC Associate to join our collaborative team in Redwood City at Bayshore Technology Park. This individual, reporting to the Director, Quality will have a proven track record of meticulous planning, clear communication, and strategic prioritization within a biotechnology, pharmaceutical, or academic laboratory setting. The candidate should have a high level of integrity and an ability to take on different roles as required in a rapidly evolving and opportunistic environment. The candidate should be able to lead independent projects and be a team player that shares the founders’ passion for bringing vaccines to patients and improving global public health. The QC Associate will primarily be responsible for quality control data review of analytical testing performed at Contract Testing Labs (CTL). This highly motivated member of the Quality Unit will support the organization through the review of in-process, release, and stability data related to microbial safety (sterility, mycoplasma, endotoxin, and adventitious agents), purity (sequencing, host cell DNA/protein and process residuals/impurities), and potency (PFUs). | 07/15/2021 |
| 8342 | Mizuho OSI Union City, CA Systems Engineer, Medical Device Master of Science Degree Exp: < 1 years |
As Systems Engineer you will be part of a small, agile team; responsible for medical device development projects starting from technology exploration, product definition, to guiding integration with software controlled electro-mechanical systems; ending with product and release testing. We develop a broad spectrum of products from sterile disposables to complex capital equipment using a customer-centric, collaborative, innovation driven approach. We value ownership, calculated risk-taking, and tolerance for ambiguity as we build future devices and improve existing products. | 07/16/2021 |
| 8343 | Moderna Therapeutics Cambridge, MA Research Associate, Immunology MS focused on biological sciences. Exp: 0-2 years |
Moderna is seeking a highly skilled and motivated Research Associate or Senior Research Associate with a background in immunology. The successful candidate will help develop ex vivo and in vivo immunology assays that support advancement of Moderna’s mRNA technology platform, investigate immune-related molecular and cellular mechanisms, and be responsible for lab equipment maintenance. She/he/they should be able to apply various immunological techniques and should have the ability to thrive in a highly collaborative, dynamic, and interdisciplinary environment. The successful candidate is expected to have substantial hands-on experience in tissue processing, complex multicolor flow cytometry acquisition and data analysis, and antibody panel design. | 07/16/2021 |
| 8344 | Moderna Therapeutics Norwood, MA Manufacturing Associate I Bachelor’s Degree in Biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical engineering, Biochemistry or rela Exp: 0-2 years |
Moderna is seeking a cGMP Manufacturing Associate for mRNA Manufacturing. This position is located at our new GMP Manufacturing site in Norwood, MA. The shifts in Large Scale Manufacturing at Moderna are: 1st shift from 6:00 am to 4:00 pm, 2nd shift from 2:00 pm to 12:00 pm and 3rd shift from 10:00 pm to 8:00 am. All shifts are on a 4x10 schedule with a weekend day requirement and are either Sunday through Wednesday or Wednesday through Saturday. The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. | 07/16/2021 |
| 8345 | Moderna Therapeutics Norwood, MA Validation Engineer I B.S. in engineering, science, or an equivalent technical field. Exp: one (1) year |
The Validation Engineer I will be responsible for the delivery of commissioning / qualification / validation deliverables, ensuring equipment and systems remain in a qualified, operational state of compliance associated with cGMP manufacturing environments. This individual will work closely with Engineering / Facilities, Equipment End Users, and Quality Assurance to investigate and resolve non-conformances encountered during qualification activities. Applicants should enjoy working in a fast-paced, dynamic, and innovative environment. | 07/16/2021 |
| 8346 | MP Biomedicals Solon, OH Production Chemist BS/BA or MS in Chemistry, Biochemistry, or Biology Exp: 1-5 years |
Responsible for a wide variety of tasks as a production chemist on multiple product lines in various manufacturing areas including Diagnostics, Immunobiology, Quality Control and Molecular Biology. | 07/16/2021 |
| 8347 | Molecular Templates Austin, TX Associate Scientist, Downstream Process Development Degree in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry field or similar field of study. Exp: one (1) year |
Molecular Templates is seeking an experienced and highly motivated professional to support downstream process development. The Associate Scientist will be responsible for working with fellow team members to develop robust, efficient, and scalable methods for protein purification/manufacture. This position will perform functions related to downstream process development of recombinant biologics, including experimentation involving protein purification, cell lysis, clarification, chromatography, ultrafiltration, diafiltration and filling. Additional activities will include solution preparation, equipment maintenance and calibration, data management, report authoring, and review of manufacturing processes. This position will also aid in identifying continuous process improvement areas and technology transfer. This will require excellent technical, analytical and organizational skills, along with adherence to written and verbal instructions, and accurate and timely completion of experimental records. | 07/16/2021 |
| 8348 | DPT Laboratories [Viatris] San Antonio, TX QA Analyst I Bachelor’s degree from an accredited four-year college or university is required. Exp: 0-2 years |
Key responsibilities for this role include: Responsible for providing guidance and feedback to both internal and external customers to ensure Quality Systems requirements are met. Supports Quality Systems investigations and the facilitation of review/closure of associated records, including corrective and preventive actions (as applicable). Perform final Quality Systems review and release of raw materials/components. Facilitate change control records and their associated action items for implementation and closure. Place and maintain Quality holds (product, controlled documents, test standards) as required. Provide support for maintaining weekly/monthly internal Quality metrics Support internal, client, and regulatory audit requests as required. Within area of responsibility, understand and comply with all safety, environmental and quality practices and procedures as outlined in organizational/departmental guidelines and SOPs as well as applicable federal, state and local regulations. Perform other duties as assigned | 07/16/2021 |
| 8349 | DPT Laboratories [Viatris] St Albans, VT Chemist Bachelor of Science Degree Exp: one year |
Key responsibilities for this role include: Perform testing and inspections of various components, intermediates and finished products. Develop expertise in physical and chemical testing of adhesives and adhesive products. Assist in the development of analytical methods. Document activities and check documentation of other laboratory personnel. Assist in the investigation of aberrant results. Provide written summary reports of such investigations. Calibrate laboratory equipment as necessary. Draft protocols, technical reports, changes to SOPs, STMs. Train new laboratory personnel on test methods as required. | 07/16/2021 |
| 8350 | DPT Laboratories [Viatris] St Albans, VT 2nd shift Chemist Bachelor of Science Degree. Exp: one year |
Key responsibilities for this role include: Perform testing and inspections of various components, intermediates and finished products. Develop expertise in physical and chemical testing of adhesives and adhesive products. Assist in the development of analytical methods. Document activities and check documentation of other laboratory personnel. Assist in the investigation of aberrant results. Provide written summary reports of such investigations. Calibrate laboratory equipment as necessary. Draft protocols, technical reports, changes to SOPs, STMs. Train new laboratory personnel on test methods as required. | 07/16/2021 |
| 8351 | NanoString Seattle, WA Manufacturing Research Associate I - R - 100865 BS in Molecular Biology, Biochemistry, or related life science. Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. This position is Non-Exempt. | 07/16/2021 |
| 8352 | NanoString Bothell, WA Manufacturing Research Associate I - R - 100939 BS in Molecular Biology, Biochemistry, or related life science. Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. This position is Non-Exempt. Requirements: BS in Molecular Biology, Biochemistry, or related life science, or 2-year degree plus relevant experience 0-2 years of hands-on laboratory experience in a medical device, biotechnology, or academic setting Strong analytical, organizational, documentation and communications capabilities Ability to handle multiple tasks and meet defined deadlines Ability to lift and carry 20-25lb freezer/refrigerator racks Willing to work a flexible shift schedule. | 07/16/2021 |
| 8353 | NanoString Seattle, WA Manufacturing Research Associate I - R- 101021 BS in Molecular Biology, Biochemistry, or related life science. Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. This position is Non-Exempt. | 07/16/2021 |
| 8354 | Fujirebo Diagnostics Malvern, PA Associate Analytical Development Scientist B.S. in Biological Sciences or Chemistry. Exp: 1 year |
The individual will assist with the analytical study design, performs testing and analyses to support new product launches which includes design verification, other designated analytical protocols, and summary reports adhering to appropriate regulatory guidance, specifically CLSI. | 7/4/2021 |
| 8355 | Fulcrum Therapeutics Cambridge, MA Research Associate I or II, Muscle Biology BS/MS in biology, molecular and/or cellular biology. Exp: 1-3 years |
We are seeking a highly motivated, do it all research associate to join our efforts in the Discovery Biology group at Fulcrum to participate in building our next generation Muscle Biology platform. This individual will contribute across programs to scientific efforts focused on interrogating disease biology focused on understanding cell state dysregulation inherent to the dystrophic microenvironment. | 7/4/2021 |
| 8356 | Global Blood Therapeutics South San Francisco, CA Research Associate II: Translational Biology BA/BS in biochemistry, molecular biology or equivalent discipline. Exp: 1-3 years |
The Biology Department at Global Blood Therapeutics is looking for a qualified Research Associate with experience troubleshooting and protocol development experience. This position will be primarily responsible for supporting critical instruments, supporting internal animal studies across pipeline programs, and writing protocols around instrument care. The applicant will also provide logistics and troubleshooting support for animal and clinical studies conducted externally. An ideal candidate will be detail-oriented, organized, and comfortable working both independently and within a team. | 7/5/2021 |
| 8357 | Global Blood Therapeutics South San Francisco, CA CONTRACT - Research Associate: Translational Biology BA/BS in biochemistry, molecular biology or equivalent discipline. Exp: 1-2 years |
The Biology Department at Global Blood Therapeutics is looking for a qualified Research Associate with experience in assay development and biomarkers. This position will be primarily responsible for biochemical and cell-based assays to support animal studies across multiple pipeline programs. The applicant will also provide logistics and troubleshooting support for animal and clinical studies conducted externally. An ideal candidate will be detail-oriented, organized, and comfortable working both independently and within a team. | 07/05/2021 |
| 8358 | Genentech Washington, Research Associate Bachelor’s, Master’s or PhD degree in Biological/Life Sciences, Chemistry, Organic Chemistry, Chemical Engineering, Biochemistry or related field. Exp: 1+ years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its unique chemistry that advances DNA sequencing by nanopore, Sequencing by eXpansion (SBX™). You will develop, process and purify the molecular building blocks for our novel technology. These building blocks translate DNA sequences into a simple to measure surrogate, the Xpandomer, which significantly improves the accuracy and throughput of nanopore sequencing. The Molecular Engineering group is passionate about the novel molecules they have developed and the impact SBX technology can have on advancing sequencing and patient outcomes. We are looking for people who are excited to collaborate with us to make SBX successful. Please include a cover letter outlining why you want to work with us, your specific interest in our technology and how you would contribute. | 07/05/2021 |
| 8359 | GeneDx Gaithersburg, MD Lab Technician, DNA Extraction (FT, 40 hours) BS degree in medical technology, or related life science. Exp: (0-1) year |
GeneDx is a rapidly growing CAP and CLIA certified diagnostic genetic testing laboratory for molecular genetics. Our historic mission has been to make clinical diagnostic testing available for people with genetic conditions and their families. We apply cutting edge technologies that provide a wide array of molecular genetic diagnostic tests, including whole exome sequencing and next-generation sequencing panels. We specialize in genetic testing for rare hereditary disorders, but also test for common disorders. To learn more about GeneDx, please visit our website at www.genedx.com. | 07/05/2021 |
| 8360 | GeneDx Gaithersburg, MD Lab Technician, Next Gen (FT, 40 hours) BS degree in medical technology, or related life science. Exp: (0-1) year |
GeneDx is a rapidly growing CAP and CLIA certified diagnostic genetic testing laboratory for molecular genetics. Our historic mission has been to make clinical diagnostic testing available for people with genetic conditions and their families. We apply cutting edge technologies that provide a wide array of molecular genetic diagnostic tests, including whole exome sequencing and next-generation sequencing panels. We specialize in genetic testing for rare hereditary disorders, but also test for common disorders. To learn more about GeneDx, please visit our website at www.genedx.com. | 07/05/2021 |
| 8361 | GeneDx Gaithersburg, MD DNA Sequencing Lab Technologist I/II (FT, 40 hours) BS degree in medical technology, or related life science. Exp: 1+ year |
GeneDx is a rapidly growing CAP and CLIA certified diagnostic genetic testing laboratory for molecular genetics. Our historic mission has been to make clinical diagnostic testing available for people with genetic conditions and their families. We apply cutting edge technologies that provide a wide array of molecular genetic diagnostic tests, including whole exome sequencing and next-generation sequencing panels. We specialize in genetic testing for rare hereditary disorders, but also test for common disorders. To learn more about GeneDx, please visit our website at www.genedx.com. | 07/05/2021 |
| 8362 | GeneDx Gaithersburg, MD Cytogenetics Technologist III (FT, 40 hours) MS degree in related field. Exp: 1+ year |
GeneDx is a rapidly growing CAP and CLIA certified diagnostic genetic testing laboratory for molecular genetics. Our historic mission has been to make clinical diagnostic testing available for people with genetic conditions and their families. We apply cutting edge technologies that provide a wide array of molecular genetic diagnostic tests, including whole exome sequencing and next-generation sequencing panels. We specialize in genetic testing for rare hereditary disorders, but also test for common disorders. To learn more about GeneDx, please visit our website at www.genedx.com. | 07/05/2021 |
| 8363 | GeneDx Gaithersburg, MD Bioinformatics Engineer I (FT, 40 hours, Remote) BS or MS in bioinformatics, computer science, or a related discipline. Exp: 1-3 years’ |
We are seeking a Bioinformatics Engineer to join our team supporting clinical next-generation sequencing tests within GeneDx. In this role you will join our software operations team, working closely with our laboratory and scientific staff, and fellow developers on the Data Science team to assess, investigate, and resolve data-related questions and other issues that arise during our production clinical testing. You will also monitor our production pipelines, tracking system stability, implementing code improvements, and assisting with both software and qualitative validations. You will learn and follow internal guidelines for good software management and release practices, as well as taking time for team-based code review, optimization, and continued learning. | 07/05/2021 |
| 8364 | Grand River Aseptic Manufacturing Grand Rapids, MI Microbiology Technician (2nd or 3rd Shift) Bachelor’s Degree in Microbiology or a related field. Exp: 0-2 years’ |
Supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. | 07/07/2021 |
| 8365 | Greenlight Biosciences Medford, MA Research Associate Analytical Sciences B.S. or M.S. in chemistry, biochemistry, or equivalent. Exp: 0-4 years |
GreenLight Biosciences is a venture-backed company that has developed a proprietary scalable process for the low-cost production of RNA. GreenLight is focused on developing RNA-based agricultural and human health products in an economical, sustainable and environmentally friendly manner. These products have the potential to radically change the current status quo in both market areas. We are rapidly expanding our R&D team and are seeking an exceptional, highly motivated Research Associate to play a key role in supporting the production of our next RNA-based products, transforming agriculture and vaccine manufacturing. The Research Associate will work within the Analytical Sciences team to support mRNA platform development by closely supporting and collaborating with the Process Development team at GreenLight. As a valued team member, the Research Associate will perform a range of bioanalytical assays to quantify and characterize raw materials such as plasmid DNA, mRNA products, and intermediates of the production process. This role allows learning of new methodologies and cutting-edge science, exposure to molecular biology and characterization techniques. The Research Associate will implement the testing with high accuracy and commitment to quality to produce highly reliable results instrumental in R&D discovery and mid- to late phase product development within a highly collaborative team. | 07/07/2021 |
| 8366 | Greenlight Biosciences Medford, MA Research Associate Process Development A.S. or B.S. or M.S in Chemical Engineering, Biological Engineering, or equivalent. Exp: 0 - 4 years |
GreenLight Biosciences is seeking exceptional, highly motivated Research Associate to work on the development of cutting-edge fermentations and/or cell free bioprocessing technology. The successful candidate will work hands-on in small teams to execute fermentation/cell free bioprocessing and other associated bioprocess unit operations (such as homogenization, pasteurization, centrifugation, ultra-filtration/defiltration, microfiltration, depth filtration, focusing on recovery of large molecules). A high degree of flexibility, creativity and initiative is essential for success. Strong technical, organization, communication, inter-personal, and trouble shooting skills are essential. The RA will comply with company policies and practices for EHS and will support company and organizational targets and functional growth plans. | 07/07/2021 |
| 8367 | Greenlight Biosciences Woburn, MA Research Associate1, Organic Chemistry BS or MS in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or related disciplines. Exp: 0-1 years |
GreenLight Biosciences is looking for an exceptional, highly motivated Entry Level Research Associate to support drug product developmental effort in the space of nucleic acid delivery. The ideal candidate will support mainly activities related to synthesis of new lipids, their purification and characterization (NMR and Mass Spectrometry, etc..) as well as formulation and testing of those lipids in different delivery matrices. The candidate will be part of the formulation team and will work closely with scientists and associates to support project needs. The applicant should enjoy working in a very fast -paced, dynamic, and innovative environment. The successful candidate will be responsible for performing experiments, analyzing data, and maintaining a high-quality laboratory notebook. | 07/07/2021 |
| 8368 | Greenlight Biosciences Medford, MA Quality Control Bioassay Analyst MS degree. Exp: 1 – 2+ years |
The GreenLight team is looking for a high-performing, self-motivated individual who works well in a fast-paced environment in a leading-edge biotech company. The company is looking for a key individual to play a pivotal role in advancing breakthrough therapies to rapidly address emerging pathogens. Reporting directly to the QC Laboratory Sr. Manager, the individual will be a key contributing member of our Life Science Team. The position will assist in establishing and running a Quality Control (QC) Laboratory providing support to the advancement of mRNA based human vaccines and other RNA based therapeutics. The ideal candidate will have the skills and experience necessary to build and equip a QC laboratory capable of supporting development, pre-clinical, clinical, and eventual post-marketing approval analytical testing. | 07/07/2021 |
| 8369 | Grifols San Diego, CA Research Associate 1 BS. degree in Biochemistry, Chemistry, Microbiology, Biology or other life science field. Exp: entry level |
This role supports the research function by assisting with basic research projects such as glassware and reagent needs of Grifols Diagnostics R&D lab functions by processing glassware and other technical materials in a GLP-compliant method. The research projects could be in molecular biology, immunology, microbiology or biochemistry. This is an entry level position for someone with limited experience. Prepares and weighs samples for testing and analysis. May setup and conduct tests, assays, and other protocols under the direction of an R&D scientist. Follow Standard Operating Procedures (SOPs) and Good Laboratory Practices (GLPs). Ensure all laboratory equipment and work areas are clean, sterile, and in proper working order. Responsible for calibration of instruments where needed, as well as ordering and restocking lab supplies/chemicals. | 07/07/2021 |
| 8370 | Grifols Clayton, NC Assistant/Associate Biologist, QC BS/BA degree in a life science field, medical technology, or related curriculum. Exp: 0-1 years |
Performs biological testing of moderate to advanced complexity within a Quality Operations Laboratory in a safe, accurate, and efficient manner following established written procedures while maintaining complete and accurate records of the work and results. This testing is required for the release of raw materials, in-process materials, and final containers. | 07/07/2021 |
| 8371 | GlaxoSmithKline Rockville, MD Associate QC Biochemist B.S. degree in a science field required. Exp: 0-2 years |
Are you looking for an Associate QC Biochemist role that allows you to grow professionally and contribute to the development of best-in-class medicines? If so, this role could be an exciting opportunity to explore. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Coordinate routine in-process biopharmaceutical materials, bulk biopharmaceutical ingredient, finished biopharmaceutical product and stability sample testing with testing labs. Conduct and documents routine immunology, molecular biology analytical testing for in-process, release and stability samples per SOP. Operate and mainatin QC laboratory equipment/instrument in a cGMP-compliant manner. Advanced knowledge in cGMP, CFR and other regulations in order to assure laboratory compliance. Evaluate laboratory SOPs and recommend improvement opportunities to maintain compliance with corporate and regulatory guidelines. Develops or revises laboratory SOPs as required. Assist in investigation and assay trouble shooting. Assist in critical reagent qualification/re-qualification, in immunology, biochemical, and other analytical method qualification/validation/transfer. Meet lab safety requirements. Trained as an Self Inspector Auditor and participate in >25% of department’s Self Inspections. | 07/07/2021 |
| 8372 | GlaxoSmithKline King of Prussia, PA QA Coordinator BS or BA degree in Biology, Chemistry, Engineering, Biochemistry, Computer Science, Computer Engineering, or related technical field. Exp: 1+ year |
As a QA Coordinator, you will provide support to the site when implementing new products, review of records to ensure compliance with local and regulatory guidelines, and to execute Quality Systems actions. This role may develop, implement, and administer input and in-process electronic quality systems for the production of biopharmaceutical products to ensure compliance with GSK internal procedures, policies, standards, and worldwide regulatory expectations. This role will act as advisor, facilitator, and team member regarding regulatory compliance and quality systems for all aspects of manufacturing of biopharmaceutical products. This is accomplished through direct intervention between this role and other staff in the facility. This role provides quality decisions to project teams and to routine operating teams. This position will provide guidance and training to new and existing employees in the Quality Assurance department and assist them with decision making. | 07/07/2021 |
| 8373 | GlaxoSmithKline Hamilton, MT Manufacturing Associate Bachelor’s degree. Exp: 1 year |
As a Manufacturing Associate you will be perform duties as assigned with respect to quality, timeliness, quantity and cost. Work individually and as a team to deliver cGMP compliant product. Adhere to GSK policies, procedures and support site goals. Complete documentation in line with regulatory, GSK, and departmental requirements. Work and communicate closely with other departments both inside and outside of the Value Stream. Train and mentor less experienced staff. Work with minimal supervision and coordinate complex tasks between departments. Oversee and coordinate equipment related task and issues. Demonstrate ability to cross train in multiple disciplines across the Value Stream and participate in cross functional teams. Takes initiative, provides accurate “right the first time” work and practices good time management in a fast paced, ever changing environment. Demonstrates an in-depth knowledge of the job. | 07/07/2021 |
| 8374 | GlaxoSmithKline Rockville, MD Associate QC Chemist B.S. / B.A. degree. Exp: 0 – 2 years |
Are you looking for a new challenge to drive and improve quality control testing, with a chance to broaden your leadership skills? If so, this Associate QC Chemist role could be a great opportunity to consider. The Associate QC Chemist is responsible for performing quality sampling, testing and data review for raw materials under cGMP conditions. The role will support the manufacturing campaigns by ensuring raw materials testing completion within established timelines. The role will also support operation and maintenance of QC laboratory equipment/instrument to comply with cGMP regulations. | 07/07/2021 |
| 8375 | GlaxoSmithKline Rockville, MD Associate Biochemist BS degree in a science-related field. Exp: 0-2 years |
Are you looking for a new challenge to drive and improve quality control testing, with a chance to broaden your leadership skills? If so, this Associate Biochemist role could be a great opportunity to consider. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following… Tests, documents, reports, and provides second chemist review for stability samples. Interprets compendia and internal monographs, NDAs and GSK Quality Standards. Leads and documents investigations according to established procedures and recommends corrective actions. Advanced knowledge in cGMP, CFR and other regulations in order to assure laboratory compliance. Evaluate laboratory SOPs and recommend improvement opportunities to maintain compliance with corporate and regulatory guidelines. Develops or revises laboratory SOPs as required. Prepare laboratory reagents, standards, and solutions for test procedures. Calibrates or verifies laboratory equipment. | 07/07/2021 |
| 8376 | Harpoon Therapeutics South San Francisco, CA RESEARCH ASSOCIATE/SR RESEARCH ASSOCIATE/SCIENTIST (IN VIVO), Translational Medicine BA/BS or MS (Research Associate) Exp: 1+ years’ |
We are looking for a highly motivated Research Assoc./Sr. Research Assoc./Scientist to join our Translational Medicine group to execute preclinical studies and provide in vivo proof-of-biology data on Harpoon’s drug candidates, demonstrate in vivo mechanisms of action, as well as scientific rationale to support combination clinical trials. This position is laboratory based with the successful candidate collaborating across groups to plan, execute and analyze in vivo studies. | 07/07/2021 |
| 8377 | Harpoon Therapeutics South San Francisco, CA RESEARCH ASSOCIATE, BIOLOGY BS or MS in Cell Biology, Biochemistry, or a related field. Exp: 1+ years |
The Research Biology group at Harpoon Therapeutics seeks a Research Associate to join our team. Responsibilities include testing of samples in support of both preclinical development and clinical programs, assay development and optimization, and collection of data in support of regulatory filings. Applicants should be capable of working flexibly and expeditiously in a collaborative, innovative and inspiring environment. The ideal candidate will have experience with mammalian cell culture, stable cell line generation, luciferase assays, flow cytometry, and bioassay automation. Good communication skills, good planning, and an ability to meet deadlines are essential. | 07/07/2021 |
| 8378 | HDT Bio Seattle, WA Research Associate - Molecular Biology BS/BA, or equivalent in a biological discipline. Exp: 0-3 years |
HDT Bio is pioneering technologies that direct the host immune system to treat or prevent cancer and infectious diseases. The research associate will be primarily responsible for working on the development and characterization of our RNA technology. You will have the opportunity to work closely with molecular biologists, virologists, immunologists, and material scientists to optimize formulation and delivery of RNA with specific applications in areas of vaccine and therapeutic development. A background in molecular biology is required. Major techniques include plasmid preparation, RNA transcription/capping, and cell culture. Experience with animals is preferred. | 07/07/2021 |
| 8379 | HelixBind Boxborough, MA Formulation Technician Certificate, Associate’s or Bachelors’ degree in a science or engineering discipline. Exp: 0-5 years’ |
We are seeking an energetic and self-motivated formulation technician to drive forward product development. Specific emphasis will be given to those applicants interested in a challenging opportunity with immense impact and who flourish in a fast-paced environment. The formulation technician will manage the production inventory, produce/fill/seal builds of reagents into HelixBind’s proprietary disposable test cassette, will actively communicate with management and co-workers and will maintain a safe, organized, and clean work environment. | 07/07/2021 |
| 8380 | Helomics Pittsburgh, PA Laboratory Technologist with Experience in Cell Culture and High Throughput Screening BS with a major in a biological or related science. Exp: 1+ years |
This position will contribute to tissue culture related activities involved with delivering high quality cells for use in assay development, High Throughput Screening, High Content cell-based assays, compound profiling, technology evaluations, and other objectives requiring delivery and maintenance of live cell cultures and/or frozen cell banks. These activities will be in addition to the other standard aspects of clinical lab testing. As a Laboratory Technologist in a high complexity clinical laboratory, the individual is expected to also participate in the day-to-day operational activities of the Helomics laboratory: Chemoresponse testing DNA and RNA extraction, PCR, NGS, and microarray processing. Applied laboratory automation Cell and Tissue Imaging Histology and automated immunohistochemistry | 07/07/2021 |
| 8381 | Hexagon Bio Menlo Park, CA Research Associate, Cancer Biology BSc or MSc in molecular and cellular biology or related discipline required. Exp: 1+ years |
We are searching for a high-caliber Research Associate to help drive our oncology drug development efforts. The successful candidate will function within a fast-moving environment, collaborating with an interdisciplinary team to design and execute experiments aimed at uncovering compound/target relationships and downstream phenotypes. You will also have regular opportunities for scientific presentation. As a member of the drug discovery team, the successful candidate will report directly to a Cancer Biology Scientist, and is expected to maintain accurate and meticulous records of experimental protocols and data, assist in common laboratory operations, and maintain a safe and efficient work environment. | 07/07/2021 |
| 8382 | Hexagon Bio Menlo Park, CA Research Associate, Cell Biology and Drug Discovery B.S. in biology or equivalent field. Exp: 1 year |
We have an opportunity for an exceptional cell biologist to join our growing drug discovery team. At Hexagon, you will be an integral part of a dynamic interdisciplinary team focused on developing next generation medicines. You will use your strength as an experimentalist to assist in designing, developing and optimizing target specific cell assays. You will work with senior scientists to plan, execute, and analyze your experiments and present your results. | 07/07/2021 |
| 8383 | Homology Medicines Bedford, MA Research Associate , Pilot Plant MS&T BS/MS in chemical/biochemical engineering or biology/biochemistry. Exp: 1 - 3 years |
Homology Medicines seeks an outstanding researcher in the upstream process development group to assist in the development of viral manufacturing processes. The individual in this role will be highly motivated, enthusiastic and brings rigor and a desire to deliver on tasks with focus on the development and scale up of cell-based methods for producing AAV vectors. We seek candidates with proven ability to work independently after initial training and collaboratively to achieve optimized project plans, with the goal to deliver products that transform the lives of patients. | 07/08/2021 |
| 8384 | Homology Medicines Bedford, MA Quality Control Associate Molecuar Biology Shift (Mon - Fri) Bachelor’s degree in life sciences, engineering, or equivalent. Exp: 0-2 years |
The HMI Quality Control (QC) Associate will be responsible for supporting the routine in process, release, and stability capabilities of the QC Laboratory for internally manufactured gene therapy and gene editing therapeutics. The individual will work cross-functionally to support execution of routine analytics program for GMP operations of a Clinical Phase 1/2 manufacturing facility. | 07/08/2021 |
| 8385 | Incyte Wilmington, DE Research Scientist, Chemistry Bachelor’s Degree in Organic Chemistry. Exp: 0-3 years |
Our Discovery Chemistry group is looking for an experienced Chemist. The Research Scientist develops and optimizes chemical reactions for the synthesis of novel compounds to support SAR. | 07/09/2021 |
| 8386 | Integral Molecular Philadelphia, PA Research Associate (Job ID# 090306) Bachelor’s degree in biology, bioengineering, or a related field is required. Exp: 1–2 years |
Our company is in an exciting growth phase where we are launching new products and reaching new markets. To support our growth, we seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. | 07/09/2021 |
| 8387 | Integral Molecular Philadelphia, PA Research Technician (Job ID# 062319) Associate or Bachelor’s degree in Biology, Chemistry, medical technology or related field. Exp: 6 months – 2 years |
We seek an entry level Laboratory Technician to perform vital laboratory tasks to support the continued success of our research teams. The candidate will be part of a lab management team that works in a unified and collaborative manner to ensure the efficient operation of the laboratory. | 07/09/2021 |
| 8388 | Inzen Therapeutics Cambridge, MA Research Associate, Drug Discovery Team ?Bachelor’s degree in Biochemistry, biology, molecular biology, or a related field. Exp: 0-3 years |
Due to the expansion of our R&D capabilities, we are currently on the hunt for a Research Associate to support our research in Drug Discovery team. As a Research Associate, you will work with Scientists and other team members to drug discovery efforts. You will be generating and maintaining mammalian cell lines as well as conducting various cell-based and biochemical assays based on established protocols. Inzen Therapeutics offers the challenge and opportunity to work at an early stage, big concept biotechnology company. Your efforts will enable our teams to discovery novel targets that could need to the development of a life-changing therapies. | 07/09/2021 |
| 8389 | Janssen Pharmaceuticals [Johnson&Johnson] Spring House, PA Associate Scientist, Biophysics MS degree in biochemistry, analytical chemistry, biophysics, structural biology, or related fields. Exp: 1-3 years |
The Associate Scientist will be part of a team of scientists utilizing a broad spectrum of biophysical techniques to characterize physical attributes of therapeutic assets developed by JBIO, from initial hit generation through lead molecule selection, concluding in the delineation of the biophysical and structural quality of clinical candidates entering the development portfolio. The Associate Scientist is a laboratory-based position that will contribute to the Biophysics team by conducting binding affinity and kinetic assays, such as Surface Plasmon Resonance (SPR) and Biolayer Interferometry (BLI). The Associate Scientist might conduct additional characterizations to assess protein purity and stability using chromatography, light scattering, spectrometric and calorimetric techniques. The associate Scientist will collect, interpret, and report a range of biophysical data and present to manager and project teams in order support lead molecule selection. The associate Scientist is expected to be self-driven, organized, and have excellent analytical and interpersonal skills. | 07/09/2021 |
| 8390 | Janssen Pharmaceuticals [Johnson&Johnson] Spring House, PA Associate Scientist I Bachelor’s degree in Biochemistry, Enzymology, Chemistry, Biophysics, Pharmacology or a related scientific discipline is required. Exp: 1 year |
Discovery Sciences (DS) organization is committed to the delivery of high-quality chemical leads needed for the generation of small molecule clinical compounds in all five Janssen Therapeutic Area (TA) discovery teams. This mission requires deep scientific expertise in a number of disciplines, including chemistry, cellular and molecular pharmacology, enzymology, and screening technologies coupled with an ability to work collaboratively with internal and external partners. Building on a strong legacy of success, we are currently seeking an outstanding individual to join our team as an Associate Scientist I in the Enzymology group. This position will report to a senior member of the Lead Discovery and Mechanistic Pharmacology team. The Associate Scientist I will be a key member of the Enzymology group in Lead Discovery and Mechanistic Pharmacology and will provide enzymology/biochemistry support and expertise to a variety of TA programs from target nomination through declaration of a clinical candidate. This individual will characterize enzyme function, develop innovative biochemical and biophysical assays, collaborate closely with our automation team to execute high-throughput screens to discover novel inhibitors and perform mechanistic studies to learn how they work. Deliver inhibitor potency and mechanistic data to enable optimization of lead chemical series and drive project progression. Collaborate in a highly multidisciplinary, matrix environment and be responsible for the clear communication of biochemical data to a diverse array of stakeholders on project teams. | 07/09/2021 |
| 8391 | Janssen Pharmaceuticals [Johnson&Johnson] San Diego, CA Associate Scientist, Discovery Chemistry (Multiple Openings) - La Jolla, CA Master’s Degree in synthetic organic or medicinal chemistry, or to be completed within 6 months, is required. Exp: (1+ years) |
The Discovery Chemistry group is committed to the delivery of high-quality drug candidates working with all six Janssen Therapeutic Areas (TA) discovery teams. This mission requires deep scientific expertise in a number of disciplines including chemistry, cellular and molecular pharmacology, enzymology, and screening technologies coupled with an ability to work collaboratively with internal and external partners. Building on a strong legacy of success, we are currently seeking an outstanding individual to join our team as Associate Scientist, Discovery Chemistry. We are seeking an experienced Bachelor’s- or Master’s-level medicinal chemist with excellent organic synthesis expertise to advance small molecule drug discovery programs toward the clinic. In this laboratory-based position, the successful candidate will partner with both internal and external medicinal chemistry teams to generate innovative solutions to synthetic and medicinal chemistry challenges within the context of small molecule drug discovery projects. She/he will maintain close interactions with computer assisted design scientists and biologists. Strong people skills and the ability to thrive in a team and goal driven environment are key attributes. This individual must also excel in communication and have strong interpersonal skills necessary to influence in a collaborative multidisciplinary environment. | 07/09/2021 |
| 8392 | Integer Salem, VA Engineer I Bachelor's degree or equivalent in a related field. Exp: 0-3 years |
The primary purpose of this position is to perform work which involves conventional engineering practice. Ensures Integer's internal and external customer expectations are met or exceeded. | 07/09/2021 |
| 8393 | JRF America Audubon, PA Scientist I/Entry Level Chemist Bachelor of Science or advanced degree from an accredited college or university in chemistry or other science-related field. Exp: 1-3 years |
JRF America, a member of the JRF Global group, established in 2008 is a Fully Independent Contract Research Laboratory (CRO) specialized in a higher tier regulatory chemistry services to the agrochemical sector. Our extensive expertise includes managing large study programs, field study components & understanding regulatory needs at a state, national, and international level. Studies are performed in accordance with GLP guidelines. We have the latest and most sensitive analytical instruments including HPLC/UPLC instruments with Sciex 4000 and 6500 Q Trap Mass Spectrometers, and a B-Ram radio analysis detector, to name a few. JRF America strives to employ a varied and diverse range of dynamic people who understand and appreciate the importance of our mission and what we do. When you consider an opportunity at JRF America you will be joining a dedicated and professional group. | 07/09/2021 |
| 8394 | Editas Medicine Cambridge, MA Research Associate I/II, iPSC Biology Team Bachelors or Masters in cell biology, immunology, or related field. Exp: 1-4 years |
Editas Medicine is seeking a motivated research associate to support the development and progression of a new class of cellular therapies based on CRISPR-Cas gene edited induced Pluripotent Stem Cells (iPSCs). This associate will work closely with the iPSC Biology Team Leader to culture, reprogram, differentiate and characterize iPSC cells for our immuno-oncology programs. Previous experience culturing iPSC or similarly complex cell models is desired. | 6/29/2021 |
| 8395 | Editas Medicine Cambridge, MA Research Associate I/II, Lead Discovery - Clinical Cell Line Engineering BS/MS in cell biology, molecular biology or related field. Exp: 1-3+ years |
Editas Medicine is seeking a highly motivated Research Associate I/II to join our team and advance Editas’ cell-based medicines portfolio. In this role, you will contribute to generate pre-clinical and clinical genetically engineered induced pluripotent stem cell (iPSC) lines and develop a clinically compatible, cutting-edge platform to edit, isolate and characterize clonal cell banks. The ideal candidate should have a background in gene-editing, cancer biology and a solid cell culture experience. Automation of cell culture, including the use of liquid handling robots and microplate handlers will be involved. The successful candidate will perform his/her responsibilities both at the Cambridge location and at a cleanroom in Waltham and will interact with the Sequencing, Quality and CMC/manufacturing teams as well as iPSC differentiation and genotoxicity groups. The successful candidate should demonstrate strong work ethic and enjoy working in a fast-paced and team-oriented work environment. | 6/29/2021 |
| 8396 | Elektrofi Boston, MA Research Associate/Intern BS (Associate) or Junior/Senior (Intern) in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biology, Bioengineering, or a related field. Exp: 1+ years |
Elektrofi is looking for a Research Associate to join a team responsible for the development of platform formulations for Elektrofi’s proprietary microparticle production process. The Research Associate will play a key role in supporting the development of its biologics formulation platform. This individual will join an earlystage, multidisciplinary team of scientists and contribute to a variety of formulations activities in a highly collaborative environment. | 6/29/2021 |
| 8397 | Element Biosciences San Diego, CA Reagent Formulation Technician A Bachelor of Science degree in biology, biochemistry, chemistry, molecular biology, or other related life science discipline preferred. Exp: 0-2 years |
We are seeking a Reagent Formulation Technician responsible for fulfilling the manufacturing and QC of reagent consumables, updating daily usage and supplying R&D development needs. The technician will also be responsible for calibration, validation, and troubleshooting of reagent formulation equipment and instruments. | 06/29/2021 |
| 8398 | Element Biosciences Sunnyvale, CA Research Associate/Associate Scientist BS in Molecular Biology, Biochemistry, Protein Chemistry and Chemical Engineering or a related discipline. Exp: 0+ years |
We are seeking a highly motivated team player and fast learner to join our team. Good communication and organization skills are required, as well as the ability to multi-task to deliver results within a timeline. | 06/29/2021 |
| 8399 | Element Biosciences San Diego, CA Research Associate, Protein Engineering Bachelors Degree in Biochemistry, or equivalent field of study. Exp: 1-3 years |
Seeking a Scientist contributor for exciting well-funded and long-term multi-venture backed Life Sciences and IVD start-up company. Ideal candidates will work with cross-functional departments to understand enzyme requirements and build assays and characterization tools to determine if enzymes meet specifications. Candidates are expected to have the technical expertise and drive to work independently and in combination with a small team to deliver understanding and mitigations to enzyme performance and stability. Characterization methods will employ both solution-based and surface interaction-based studies. Develops advanced methods/techniques for testing and evaluation. | 06/29/2021 |
| 8400 | EMD Serono [Merck KGaA] Carlsbad, CA Process Engineer Bachelor’s Degree in Engineering. Exp: 1 year |
The Process Engineer is the single point of contact for manufacturing support of chemical purification processes running 24/7. In this role you will ensure all safety and quality standards are upheld, monitor process data real-time, troubleshoot production problems, initiate, and execute continuous improvement projects, update system documentation, and coordinate preventative maintenance activities. | 06/29/2021 |
| 8401 | Millipore Sigma Billerica, MA Associate Scientist - Exploratory Immunology Bachelor’s degree in Immunology, Biology, or related Scientific discipline. Exp: 1+ years’ |
EMD Serono is seeking an Associate Scientist to join the Exploratory Immunology team at our Billerica, MA research facility. The Associate Scientist will contribute to the discovery of drugs for treating autoimmune diseases. She/he will drive early drug discovery projects from concept generation, discovery, and validation of new targets and also to advancing established pipeline projects to the clinic. The Associate Scientist will work in a team of scientists that develops and executes innovative approaches to propose new targets and therapeutic concepts. She/he will be responsible for cellular and biochemical assay development, experimental design and troubleshooting as required. Scouring literature for relevant assays or from collaborating scientists to support target validation and drug discovery efforts would be needed. The Associate Scientist will diligently document all research, be up to date with literature, support preparation of publications for scientific journals and present their research results at internal meetings. | 06/29/2021 |
| 8402 | Millipore Sigma Bedford, MA Research Scientist Bachelor’s degree in Cell Biology, Chemical Engineering, or related scientific discipline. Exp: <1 year |
At MilliporeSigma the Research Scientist will support efforts leading to the development of novel technologies and processes for Cell Therapy manufacturing. This hands-on role will provide cell culture support for product, process, and application development projects, analysis expertise, and timely interpretation and communication of data/results. The position involves working collaboratively with a broad group of technical and non-technical personnel and is based at our Bedford, MA campus. | 06/29/2021 |
| 8403 | Encodia San Diego, CA Research Associate Chemistry MS Exp: 0+ years |
Encodia is seeking a highly motivated Research Associate to join its Chemistry team to assist in the advancement of novel chemical methods for protein analysis. The ideal candidate will have extensive experience in synthesis, isolation, and characterization of oligonucleotides and small molecules. | 06/29/2021 |
| 8404 | Encodia San Diego, CA Research Associate II/Sr. Research Associate, Chemistry and Materials MS Exp: 1 - 3 years |
Encodia is seeking to recruit a BS/MS level Research Associate with 2 - 5 years of experience in production and QC of microbead materials. The successful candidate will possess excellent lab skills in performing R&D and production operations consistently and hands-on experience in analytical tools for assessing materials and surfaces. This position will involve research and collaboration with teams that interface between material science, chemistry, and bio-conjugation on solid supports. Highly motivated candidates with a passion for innovation are encouraged to apply. | 06/29/2021 |
| 8405 | Endo Pharmaceuticals Horsham , PA QC Analyst I - Microbiology B.S. in a Biological Science or related field. Exp: 0-3 years’ |
The QC Analyst I – Microbiology will perform microbiological testing, release of in-process, intermediates and finished products, and testing for validation purposes. This role completes appropriate documentation to support testing procedures including data capture forms, equipment logbooks, and inventory forms. Additionally, this role is responsible for assisting with the writing of standard operating procedures (SOPs) and revision of existing documentation. | 06/29/2021 |
| 8406 | Endo Pharmaceuticals Horsham , PA Quality Specialist (10 hour shift) Master’s degree in science or engineering. Exp: 1+ years’ |
Member of the Quality group providing support for various aspects of Development, Phase I-IV clinical, scale-up activities and commercial manufacturing, testing and release, as applicable. The Quality Specialist assists with internal and external quality operations and systems, such as facility/equipment, utilities, materials, production, laboratory, packaging/labeling, and general compliance as applicable, and helps assure compliance with current domestic and international GMPs and regulatory agencies. The Quality Specialist may monitor, track and trend Non-Conformances, CAPA and other quality systems, assesses the risk level associated with Non-Conformances and escalate the issue to management. This role is responsible for initiating self-audit checks and evaluation of CAPA effectiveness checks. Additionally, the Quality Specialist is responsible for preparing materials for inspection readiness and management review. | 06/29/2021 |
| 8407 | Entrada Therapeutics Boston, MA Research Associate, Antibody Discovery/Protein Engineering BS/MS in Biological Science or a related field. Exp: 1+ years |
Entrada is seeking a highly motivated, collaborative, and innovative research associate with a background in antibody discovery and engineering to join Entrada’s discovery efforts. The candidate will work with world-class, multidisciplinary team of drug discovery scientists on applying cutting-edge delivery technology to develop leads for compelling intracellular biological targets. Specifically, the candidate will execute biologics against therapeutically relevant intracellular targets and contribute to scientific publications and regulatory submissions as required. | 06/30/2021 |
| 8408 | Entrada Therapeutics Boston, MA Research Associate/Senior Research Associate, Product Development and Translational Research BS/MS in biological science or related field. Exp: 1 year |
In this role you will support the formulation of therapeutic candidates and work collaboratively to coordinate in vitro and in vivo studies. You will be responsible for the formulation of test articles and ensuring that appropriate quality control tests are completed. You’ll work side-by-side with chemistry, pharmacology, neuromuscular, and analytical team members to nominate candidate selections. You will also help to coordinate with local or international CROs and consultants to support pre-IND and IND enabling studies. Additionally, you will have the opportunity to contribute to scientific publications and regulatory submissions as needed. | 06/30/2021 |
| 8409 | Enzo Life Sciences Farmingdale, NY Manufacturing Scientist I- Immunoassays MS in Molecular Biology, Genomics, Biochemistry or other similar areas. Exp: (1+ years) |
This position is responsible for the manufacturing and testing of immunoassay kits, chemicals, and reagents serving the life sciences, and ensuring product quality based on thorough science. Integral to the kit production process, the Manufacturing Scientist I will assist in all phases of kit product release, including the choice of critical raw materials, selection of release criteria, and the validation, testing, and optimizing of kit components. As part of the manufacturing team, this position will share matrixed responsibilities with team members to meet kit production goals. | 06/30/2021 |
| 8410 | Enzo Life Sciences Farmingdale, NY Production Associate Bachelor's Degree preferred. Exp: 0-2+ years |
This position is responsible for the timely and efficient scheduling and packaging of standard and custom products (specifically our saline line), and for providing support to other areas of manufacturing to ensure timely product delivery. | 06/30/2021 |
| 8411 | Epic Pharma Laurelton, NY SYSTEMS ENGINEER Master’s in Computer Science, Computer or Electrical Engineering, or Information Technology Exp: 1 year |
Maintain, implement, configure and support LAN infrastructures of both Corporate and Empower lab networks. Migration of software applications, tools and hardware systems. Cloud QAD ERP application and EDI (Electronic Data Interchange). Python/bash scripting and development of web applications (frontend, backend and database). Utilize technologies including Windows and Linux Servers and OS, AWS, HTML, CSS, Django, Python, Apache, XML, Firewall security, Office365, Active Directory, Networking, CCNA, EDI, X12 standards, Cloud ERP, Empower, Tiamo, UV Spectrum, and FTIR. | 06/30/2021 |
| 8412 | Eurofins Genomics Spring House, PA Scientist BS/MS in biology or biochemistry. Exp: 1-5 years |
The candidate for this position will lead and perform cell biology/cell culture process development in support of the Drug Product Development in Spring House, PA. | 07/01/2021 |
| 8413 | Eurofins Genomics Madison, WI Analytical Chemist I Bachelor’s Degree in relevant field. Exp: 1.5 - 2 years |
Position will be 2nd shift- Monday thru Friday, with overtime/weekends as needed. To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. | 07/01/2021 |
| 8414 | Eurofins Genomics Lancaster, PA Chemist- Eurofins Lancaster Laboratories Environmental - Lancaster, PA Bachelor’s degree in chemistry, biology, physics, or other related degree concentration. Exp: 1-3 years |
Maintain GC/MS instrumentation Tune and calibrate instrument daily Analyze quality control and client samples Review and assemble data in an efficient manner with a high degree of quality Evaluate current organizational and analytical systems Suggest and implement the necessary corrective action to ensure the above can be performed in alignment with client and/or regulatory requirements Perform all duties with minimal supervision | 07/01/2021 |
| 8415 | Eurofins Genomics New Orleans, LA Laboratory Technician Bachelor’s degree in Molecular Biology, Biochemistry, Chemistry, or a related field. Exp: 0-5 years |
Perform laboratory analysis on food, feed, and food ingredients, including sample preparation, DNA extraction, PCR, and/or ELISA assays Complete all lab assignments in a timely and accurate manner to support quality and customer commitments Follow all Standard Operating Procedures and other Work Procedures correctly Maintain a safe and clean laboratory work environment Keep accurate and timely records of work performed on a daily basis or as needed for quality control Perform QA/QC duties and maintain respective records, as assigned by the Laboratory or Quality Manager Identify method / matrix / analytical difficulties and report these to a supervisor Other duties as assigned | 07/01/2021 |
| 8416 | Eurofins Genomics Fremont, CA Cell Culture Scientist BS or MS in cell biology / biochemistry. Exp: 1 year |
The successful candidate for the Scientist I position will join the Profiling and Cell Services team with a multifaceted approach for providing high value services based on the DiscoveRx PathHunter platform and other proprietary technologies. | 07/01/2021 |
| 8417 | Eurofins Viracor BioPharma Services Foster City, CA Formulation Development Chemist M.S. degree in a related scientific field. Exp: 1-3 years |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a Formulation Development Chemist in our Professional Scientific Services group in Foster City, CA. | 07/01/2021 |
| 8418 | Eurofins Viracor BioPharma Services Summit, NJ Bioassay Scientist II Bachelor’s degree or Master’s degree in Biology (Molecular or Cell Biology), Biochemistry or other related degree concentration. Exp: 1 year |
Experience executing bioassays (cell culture related assays) and binding assays in a regulated environment Proficiency in diverse analytical techniques is required along with basic biochemistry laboratory techniques Computer competency is essential with emphasis on spreadsheet-based software. The ability to adhere to strict guidelines when applicable is required. Ability to document and review data as per established company guidelines and SOPs Expected to be able to work as a team player and take initiatives on lab management/maintenance tasks | 07/01/2021 |
| 8419 | Eurofins Viracor BioPharma Services Lake Forest , IL Analytical Chemist I BS in in Chemistry, analytical chemistry, Chemical Engineering or related field. Exp: 1+ years |
This position performs all assigned chemistry techniques with minimal supervision. This position will demonstrate a good understanding of GMP and scientific principals and their cause and effect on scientific outcomes as practice of GMP/GLP is routine. This position authors and may review other scientist’s protocols, reports, specifications and test methods and will present results at team meetings with interpretation. | 07/01/2021 |
| 8420 | Eurofins Viracor BioPharma Services Lancaster, PA Associate Scientist (Entry Level/May grads welcome) - Environmental Bachelor’s degree in chemistry, biology, physics, or other related degree concentration. Exp: Entry Level |
Associate Chemist responsibilities include, but are not limited to, the following: · Maintain GC/MS instrumentation · Tune and calibrate instrument daily · Analyze quality control and client samples · Review and assemble data in an efficient manner with a high degree of quality · Evaluate current organizational and analytical systems · Suggest and implement the necessary corrective action to ensure the above can be performed in alignment with client and/or regulatory requirements · Perform all duties with minimal supervision | 07/01/2021 |
| 8421 | Eurofins Viracor BioPharma Services St Charles, MO Associate Scientist I B.A./B.S. Exp: 6 months |
The Associate Scientist I will support the Discovery Services and Products Team in contract research services. This role requires knowledge of scientific principles and experience in a general lab setting. | 07/01/2021 |
| 8422 | Eurofins Viracor BioPharma Services Monrovia, CA Wet Chemistry Scientist I BS degree in chemistry or other related science field. Exp: 1 - 2 years |
Routine sample preparation and analysis of water samples by various written EPA and Standard Methods procedures, Performing data process, data entry and written documentation Performing routine instrument maintenance. Preparation of reagents and standards. Other general laboratory related duties as assigned Will include regular late shift and/or weekend duties. | 07/01/2021 |
| 8423 | Eurofins Viracor BioPharma Services Monrovia, CA Scientist I BS degree in chemistry and /or other related science field. Exp: 1 - 2 years |
EUROFINS EATON ANALYTICAL has a Scientist I opening at our Monrovia Laboratory in our Ion Chromatography department. This is a second shift full time position, 40 hrs/week. Responsible for routine analytical procedures in our laboratory. | 07/01/2021 |
| 8424 | Exosome Diagnostics [Bio-Techne] Minneapolis, MN Research Associate, Conjugation Bachelor’s degree in chemistry, biological sciences or equivalent (chemistry or biochemistry preferred). Exp: 0 to 2 years |
This position is responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel. | 07/01/2021 |
| 8425 | Exosome Diagnostics [Bio-Techne] Minneapolis, MN Research Associate MS/Bachelors degree. Exp: 0 - 2 years |
Bio-techne is currently seeking to fill the role of a Research Associate as it grows its gene delivery team. The Research Associate has a solid understanding of cell culture practices including cell maintenance, transfection optimization and downstream analysis including flow cytometry and western blotting. | 07/01/2021 |
| 8426 | Exosome Diagnostics [Bio-Techne] Minneapolis, MN Quality Control Research Associate B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
Perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, SEC/HPLC, endotoxin assay, and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity and team building across the QC Department or the entire company. Perform additional duties as assigned. | 07/01/2021 |
| 8427 | Exosome Diagnostics [Bio-Techne] Minneapolis, MN R&D Research Associate BS in molecular biology, biochemistry, cell biology or related field. Exp: 1 year |
We seek a highly motivated and creative research associate to join our R&D team. You will work within a highly dynamic group and be responsible for improving current products and developing new products based on RNAscope technology. | 07/01/2021 |
| 8428 | Exosome Diagnostics [Bio-Techne] Minneapolis, MN Research Associate, PAS B.S. or M.S. in life sciences and/or in molecular biology, biochemistry, cell biology or related field. Exp: 1-2 years |
This position will serve as key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic clients. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. The Research Associate must be willing to learn new techniques quickly and be able to adapt to shifting priorities in a fast-paced and growing start-up environment. This position will be based in Newark, California. | 07/01/2021 |
| 8429 | Finch Therapeutics Somerville, MA Manufacturing Associate Bachelor’s degree. Exp: 1-3 years |
The Manufacturing Associate will participate in the day-to-day operation of a GMP-compliant manufacturing facility. | 07/01/2021 |
| 8430 | Research Associate, Formulations Lexington, MA Research Associate, Formulations MS degree in Bio/Chem Engineering, Chemistry, Pharmaceutical Science, Physics or related field of study. Exp: 1+ years |
The Research Associate, Formulations, is a laboratory-based position with tremendous learning potential in the area of drug formulation development. Reporting to the Associate Director, Process Development, and working in a cross-functional team environment, the successful candidate will take part in contributing to the development of the company’s PCA technology platform and executing the company’s small-molecule combination strategy. This position will be pivotal in the successful development of pharmaceutical products based on the company’s PCA platform. | 07/01/2021 |
| 8431 | Fresenius Kabi Melrose Park, IL ASSOCIATE CHEMIST B.S. in Chemistry or equivalent previous lab experience. Exp: 0-3 years |
Responsible for the chemical analysis of raw material, in-process, stability and finished products as required for QC. Effectively communicates work and results both orally and in writing. | 07/01/2021 |
| 8432 | Fresenius Kabi Melrose Park, IL SCIENTIST, ANALYTICAL DEVELOPMENT Master of Science degree in Chemistry. Exp: 0-3 years |
The Scientist, Analytical Development conducts all aspects of Analytical Development including method development, experimentation, and record keeping, including developing and implementing methods that meet project needs. | 07/01/2021 |
| 8433 | Fresenius Kabi Grand Island, NY MANUFACTURING ENGINEER Bachelor degree in Engineering. Exp: 0-3 years’ |
Responsible for engineering project execution by cross functional team of internal and external subject matter experts to improve plant performance, capacity and quality. Under the guidance of the Manager of Engineering or Senior Manufacturing Engineer, the primary responsibility of this position is for design modifications to existing high-speed pharmaceutical manufacturing equipment and tooling in order to improve quality, optimize performance and minimize defects. This position will also be responsible for specifying and procuring new equipment and tooling, managing equipment and facilities projects from conception through completion, including determining and meeting change control requirements. Excellent written and verbal communication skills. Excellent project management skills including experience using MS Project. Experienced AutoCAD or SolidWorks user. Maintain cGMP compliance in accordance with worldwide guidance sources. | 07/01/2021 |
| 8434 | Catalyst Biosciences South San Francisco, CA Research Associate (TM21-271) Bachelor’s degree in biochemistry, chemistry, biology, bioengineering or another related field. Exp: 1+ years |
Catalyst Biosciences is seeking motivated Research Associates to join our Protein Engineering and Assay Science teams. Our new research associates will have expertise in assay development, protein expression and/or purification that will be applied to the discovery of engineered protease biopharmaceuticals in rare diseases. The position will report to a (senior) scientist in a cross-functional environment in brand new laboratories in South San Francisco. | 6/22/2021 |
| 8435 | Celldex Therapeutics Fall River, MA Quality Control Analyst I Completed Bachelor’s degree in Biology, Chemistry, or related discipline. Exp: 0-2 years |
As a Quality Control (QC) Analyst I at Celldex Therapeutics, you’ll be responsible for everything associated with routine lab work assigned by departmental management at our Fall River MA facility. If you are looking to get laboratory experience in the biotechnology / pharmaceutical industry and want to work in a small team environment with a great group, this is an opportunity you’ll want to explore! | 6/23/2021 |
| 8436 | ChromaTan Springhouse, PA ASSOCIATE SCIENTIST I Bachelor of Science degree in Chemistry, Biochemistry, Chemical Engineering or a related field. Exp: 0-2 years |
This position will support the downstream purification team for development and implementation of a fully integrated end to end continuous bio-production platform fully enabled with PAT. This position will focus on evaluating continuous operation technologies using quality by design techniques, to develop and optimize novel, continuous recovery and purification processes, for recombinant proteins and biological macromolecules. The applicant should have experience in laboratory research, and a desire to continue in a laboratory-focused role. The position will interface with a small team of scientist and engineers focused on continuous chromatography process development and technology transfer to demonstration scale production. | 6/24/2021 |
| 8437 | Clinlogix Lower Gwynedd, PA Clinical Research Associate Bachelor's degree in Life Sciences or related field (RN with evidence of further study considered). Exp: 1-3 years |
The Clinical Research Associate reports to and works under the direction of the Manager, Global Clinical Monitoring. Responsible to monitor clinical trials, study sites and clinical data while ensuring compliance with protocol and overall clinical objectives and Good Clinical Practice (GCP). Provides administrative and project support to clinical programs with minimum supervision. Interfaces with all project/clinical team members and off-site personnel as needed in support of project and departmental goals and responsibilities. | 06/24/2021 |
| 8438 | CODA Biotherapeutics South San Francisco, CA Research Associate, Cellular & Molecular Neurobiology BS or M.S. in Cell Biology or a closely related field. Exp: 1-2 years |
We are looking for a highly motivated and dynamic candidate for the role of Research Associate, Cellular & Molecular Neurobiology to join CODA’s pharmacology group. This individual will work under the guidance of a scientist to support selection and characterization of engineered ligand-gated ion channel candidates via in vitro imaging and electrophysiology assays. The ideal candidate has significant experience in neuronal primary culture, including tissue harvest, cell culture and in vitro viral vector transduction systems, and is open-minded, trainable, and enthusiastic about research. | 06/24/2021 |
| 8439 | Codexis Redwood City, CA Research Assistant, Automation & Analytics BS or equivalent in Life Science Exp: 1 ~ 3 years |
To help us reach our goals we are looking to hire Research Assistant (with focus on high-throughput, Automated Experiments) to join our Automation Engineering group within the Automation & Analytical Sciences department. | 06/24/2021 |
| 8440 | Codexis Redwood City, CA Research Assistant/Associate, Biotherapeutics Lead Discovery BS or MS Biochemistry, Structural Biology, Bioengineering or related discipline. Exp: 0-6 years |
Codexis Biotherapeutics is rapidly growing, and we are presently seeking to expand our pipeline and diversify applications of our technology platform. To help us meet these goals, we are looking to hire a Research Assistant/Associate to join our Biotherapeutics Lead Discovery Team. | 06/24/2021 |
| 8441 | Codexis Redwood City, CA Research Associate I/Process Engineer I Downstream Bioprocess Master’s degree in Biochemistry, Biological Science, Chemical Engineering or related discipline. Exp: 0-3 years |
To help us meet our goals we are looking to hire a Process Engineer I / Research Associate I to join our Downstream Bioprocess Development team. In this role, you will design, perform, and analyze DSP experiments to understand and optimize purification processes. You will also play a key role to support selection of lead therapeutic candidates for the treatment of rare genetic disorders. | 06/24/2021 |
| 8442 | Cognate Bioservices Memphis, TN Quality Ops Specialist I BS/BA Life Science or related field. Exp: 0-1 year |
Review manufacturing Batch Production Records (BPRs) and associated supporting documentation including logbooks, Quality Control (QC) testing reports, environmental monitoring reports, etc. Perform line clearance and provide general manufacturing support. Supports product shipment and receipt of returns. Support raw material review and disposition. Review Building Management Systems reports. Participate in departmental and cross-functional continuous improvement efforts. Consistently set a high standard for quality of work. Promote a safety mindset through daily actions and communication with team members. Other duties as assigned. | 06/24/2021 |
| 8443 | Cognate Bioservices Memphis, TN QC Analyst I, Microbiology Bachelor’s Degree in Microbiology. Exp: 0-2 years |
The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product-release testing, and raw material testing. The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision is essential for success | 06/24/2021 |
| 8444 | Cognate Bioservices Memphis, TN Manufacturing Associate I BS in a scientific field strongly preferred. Exp: Zero to 1 year |
The Manufacturing Associate I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays, as necessary. Must be able to meet physical requirements established in this job description. | 06/24/2021 |
| 8445 | Compass Therapeutics Boston, MA Associate Scientist I or II, Immunology BS or MS in immunology, molecular biology, biochemistry, or a similar field. Exp: 1 year |
The ideal candidate will be interested in developing creative and novel immunology-based assays for solving complex biological problems, as well as developing an understanding of therapeutic drug discovery and its applications, related to treatment of immunological based diseases including cancer. The Associate Scientist will have strong interpersonal skills and enjoy working in a truly multi-disciplinary environment, while interacting closely with colleagues and being trained by more senior scientists, in multidisciplinary teams such as immunology, platform technology, and protein engineering | 06/24/2021 |
| 8446 | CooperSurgical Livingston, NJ PGT-A Lab Technician BS/MS in Biology or related science. Exp: 1+ year |
Performs complex molecular-based procedures on clinical samples. Analyzes clinical results and provides diagnoses. Performs clinical tasks associated with clinical cases. | 06/24/2021 |
| 8447 | CordenPharma Boulder, CO QC Analyst - Corden Pharma Boulder Bachelor's degree (B. A.) from four-year college or university. Exp: one year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 06/24/2021 |
| 8448 | CordenPharma Boulder, CO QC Analyst - Nights Bachelor's degree (B. A.) from four-year college or university. Exp: one year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 06/24/2021 |
| 8449 | Crown Bioscience San Diego, CA Research Associate I - Cell Culture Technician Bachelor's degree in Biology, Biochemistry or related area. Exp: 1-2 years |
The purpose of the Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 06/24/2021 |
| 8450 | Crown Bioscience San Diego, CA Research Associate I - Cancer Biology & Immunology Requires a Bachelor's degree in Biology, Biotechnology or other relevant area of scientific discipline. Exp: 1‐ 2 years |
The purpose of the Cancer Biology Immunology - Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with company's goals, objectives and quality standards. | 06/24/2021 |
| 8451 | Crown Bioscience San Diego, CA Research Associate I - In Vivo Oncology Bachelor’s Degree in a scientific discipline. Exp: One year |
In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 06/24/2021 |
| 8452 | Crown Bioscience San Diego, CA Research Associate I - Inflammation and Immunology Bachelor's degree in Biology, Biotechnology or other relevant area of scientific discipline. Exp: 1-2 year(s) |
The purpose of the Inflammation and Immunology Research Associate I position is to perform primarily in vivo animal studies within the Inflammation and Immunology group in support of the Company's goals and objectives. | 06/24/2021 |
| 8453 | CSL Behring [Seqirus Inc] Holly Springs, NC Scientific Associate I Bachelor’s Degree in related scientific field. Exp: 0+ years |
Candidate will provide support on Technical Development Virology and Cell Culture projects of varying size and support technical projects within function. | 06/24/2021 |
| 8454 | CSL Behring [Seqirus Inc] Holly Springs, NC Scientific Associate I (Cell and Molecular Analytics) Bachelor’s Degree in related scientific field. Exp: 0-+2 years |
The Associate Scientist hired for this position will support development and testing of molecular biology assays, such as qPCR, RT-PCR, digital PCR, for the process development of seasonal and pandemic DS and DP and execution of development stability studies. | 06/24/2021 |
| 8455 | CSL Behring [Seqirus Inc] Holly Springs, NC Scientific Associate I (Separations) Bachelor’s Degree in related scientific field. Exp: 0-2+ years |
The Associate Scientist hired for this position will support development and testing of analytical separation methods for large molecules including nucleic acid and protein. The scope will include support of process and product development activities as well as the execution of developmental stability studies. | 06/24/2021 |
| 8456 | Cue BioPharma Cambridge, MA Contract Associate Scientist – Translational Immunology M.S. in a relevant field. Exp: 0-2 years |
We are looking for a motivated Contract Associate Scientist to join our Translational Immunology/Immuno-Oncology group to provide key mechanistic, pre-clinical and translational support for Cue Biopharma’s growing pipeline. The Contract Associate Scientist will be part of the company’s TCR Core, a team dedicated to generating and performing key studies with T Cell Receptors – TCR-transduced human cell lines and primary human T cells. This is a temporary contract position that could last up to six (6) months. | 06/25/2021 |
| 8457 | Culture Biosciences South San Francisco, CA Research Associate I Bachelor’s in chemistry, chemical engineering, biochemistry or a related field. Exp: 1 year |
We’re looking for a Research Associate I, Analytical Chemist who will be responsible for transferring and validating analytical methods for customer products, troubleshooting analytical equipment with minimum supervision and writing validation reports. In this role, you will impact our cloud based analytical services to accelerate the product quantification which allows our clients to make faster decisions about their product. This is a great opportunity for someone looking to grow to join a team willing to train and leverage their analytical chemistry skills. | 06/25/2021 |
| 8458 | Cytovance Biologics Oklahoma City, OK ANALYTICAL DEVELOPMENT ASSOCIATE I BS/MS in a life science field. Exp: 1+ year |
The AD Associate I/II position develops, optimizes, and qualifies analytical methods for biopharmaceutical products. The associate also supports drug development departments, such as Purification Department and Cell Culture Department, by performing analytical testing. | 06/25/2021 |
| 8459 | DeepBiome Therapeutics Kendall Square, Cambridge, MA Research Associate Master of Science or Bachelor of Science (or equivalent) in Bioengineering, Molecular Biology, Synthetic Biology, Microbiology or related field. Exp: 1-2 years |
We are seeking a Research Associate/Senior Research Associate to support our proprietary drug discovery platform. The candidate will be joining DeepBiome’s synthetic biology group and working in a cross-functional project team. Types of activities include plasmid construction and preparation, transformation and culturing, plus preparing experimental media and buffers. | 06/25/2021 |
| 8460 | Demetrix Berkeley, CA Associate Scientist BS Exp: 1-4 years’ |
Demetrix is a start up in the San Francisco Bay area that is making nature’s medicines in a smart and responsible way. We are seeking an Associate Scientist to join the Strain Engineering team. The individual in this role will be part of an interdisciplinary team of molecular biologists, fermentation scientists and engineers, automation engineers, software engineers, and analytical chemists working to rapidly develop microbial strains to produce natural product medicines. This is a full time position. | 06/25/2021 |
| 8461 | Demetrix Berkeley, CA Associate Scientist MS in Chemistry, Biochemistry, Chem. Engineering, or a related discipline. Exp: 1+ years |
You will be part of an interdisciplinary team of fermentation scientists and engineers, automation engineers, software engineers, analytical chemists, and molecular biologists to rapidly develop microbial strains to produce high value natural product medicines. The Analytical Chemistry group is an integral part of the Demetrix team, providing the rest of the company with high quality data while maintaining and balancing accuracy, precision, and throughput. As part of the Analytical Chemistry group, you will help us with operations, instrument maintenance and troubleshooting, and development of new methods while fostering an atmosphere of continued improvement and innovation. | 06/25/2021 |
| 8462 | Demetrix Berkeley, CA Process Engineer Bachelors or Masters degree in Biological/Chemical Sciences, or Engineering field. Exp: 0-2 years |
Demetrix is a three-year-old start-up in the San Francisco Bay area that is making nature’s medicines in a smart and responsible way via synthetic biology. You will be part of the Downsteam Process Development team and will assist in the development of robust, scalable downstream processes at bench-scale, and transfer these processes to pilot and manufacturing scale. You will be part of an interdisciplinary team of fermentation engineers, automation engineers, software engineers, analytical chemists, and molecular biologists working to rapidly develop microbial strains to produce natural product medicines. | 06/25/2021 |
| 8463 | Demetrix Berkeley, CA Fermentation Engineer BSc or MSc (chemical engineering, microbiology, biological/life sciences or comparable degrees). Exp: 0-3 years |
Within Demetrix you will be part of the Upstream process engineering team within the department of Manufacturing & Process Engineering. You will work closely with others to execute bench-scale fermentations to screen strains and develop improved fermentation processes. You will be part of an interdisciplinary team of fermentation/DSP scientists and engineers, automation engineers, software engineers, analytical chemists, and molecular biologists working to rapidly develop microbial strains to produce natural product medicines. | 06/25/2021 |
| 8464 | Dendreon Union City, GA Quality Specialist I, Quality Systems Bachelor’s degree in a scientific discipline or equivalent. Exp: 1-2 years |
Responsible for monitoring policies, processes, procedures and controls ensuring that performance and quality of products conform to established standards and regulatory requirements. administrating corporate document control processes for all computerized and hard copy files. Responsible for adhering to GMP regulations, cGMP’s, c GDPs and company policies. Shift will be Monday - Friday - 9AM - 5PM | 06/25/2021 |
| 8465 | Dermira[Lilly] Indianapolis, IN Associate Analytical Chemist BS/MS in Analytical Chemistry, Biochemistry, or Chemistry. Exp: 1+ years |
Bioproduct Analytical Development has an exciting opportunity for an analytical chemist to join our control strategy development group! You will be part of a diverse team of analytical chemists, pharmaceutical scientists, and purifications engineers delivering product and process understanding across a broad range of platforms. Candidates for this position will be able to: Development of analytical methods to support development of oligonucleotides, therapeutic recombinant proteins, and/or our bioproduct large molecule portfolio. Participate in the development of the control strategy for the development of oligonucleotides, therapeutic recombinant proteins, and/or our bioproduct large molecule portfolio. Responsible for evaluating and/or implementing new analytical technologies/methods to advance Lilly's current analytical capabilities for bioproduct testing with a focus on state-of-the-art separation sciences capabilities. The ideal candidate will have breadth in multiple analytical techniques. Strong technical problem-solving ability and the ability to work with cross-functional teams will be required. | 06/25/2021 |
| 8466 | Dermira[Lilly] Branchburg Township, NJ Biochemist - Quality Control (QC) BS, MS in a related science (e.g., Chemistry, Biochemistry). Exp: BS 0-5 years; MS 0-2 years |
This is a Tuesday to Saturday day shift position. Conduct routine and non-routine analyses of in-process materials, raw materials, finished goods, and stability samples by appropriate biochemical methods as assigned by Supervisor. Performs routine QC responsibilities as needed. May lead projects such as method validation activities. Applies acceptable cGMP practices during execution of all work tasks. Works independently with moderate supervisory guidance. | 06/25/2021 |
| 8467 | Dermira[Lilly] San Diego, CA Molecular Biologist Bachelor’s Degree in biochemical sciences (biology, molecular biology, or similar field). Exp: 1 year |
We are the Biotechnology Discovery Research Division at LBC-San Diego, responsible for generating, characterizing, and optimizing biotherapeutics from lead generation through lead optimization and preclinical development. Individuals on our team support cross-disciplinary efforts to engineer innovative biotherapeutics that treat metabolic, autoimmune, and neurologic diseases. Join our team of scientists working to improve lives of patients around the world. The Protein Biosciences Group at the Lilly Biotechnology Center-San Diego is seeking an associate level scientist specializing in molecular biology to join the Mammalian Protein Expression Team. We are looking for a hardworking scientist who is organized, detail-oriented and passionate about research. Do you have an in depth understanding and experience in molecular biology techniques to execute custom cloning project? Join our team and grow in your career! | 06/25/2021 |
| 8468 | Dermira[Lilly] Branchburg Township, NJ Technician - Quality Control Microbiology - FTE B.S. or M.S. in Microbiology or related sciences. Exp: 0-2 years |
Conducts routine and non-routine analyses of in-process materials, raw materials, environmental/water samples, finished goods and stability samples by appropriate microbiology methods as assigned by supervisor. Perform routine QC responsibilities as needed. Applies cGMP practices during execution of all work tasks. Exhibits strong teamwork skills. Performs routine QC Microbiology responsibilities as it relates to the water/ EM group as assigned by supervisor. | 06/25/2021 |
| 8469 | Dyno Sense San Jose, CA QA Engineer BS Degree in Computer Science, Engineering, or a related subject. Exp: 0-2 years |
Estimate, plan, and coordinate testing activities. Develop test plan, test cases, test scenarios based on Users Stories and product’s design description to meet business requirements and technical specifications Perform ad hoc, functional, integration, and regression testing Identify software defects and submit problem reports via bug-tracking system Perform regression testing on fixed issues | 06/25/2021 |
| 8470 | EAG Laboratories Santa Clara, CA Research Associate - Materials Science Bachelor's degree in chemistry, or other related degree concentration. Exp: 1 – 2 years |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a Research Associate to work in our Professional Scientific Services group in Santa Clara, California supporting the materials team in developing polymeric materials to support emerging technologies. | 06/25/2021 |
| 8471 | EAG Laboratories San Diego, CA Molecular Biologist Associate - Automation B.S. in Biological sciences (Molecular Biology, Biotechnology, Immunology, Biochemistry, or similar field). Exp: 1-5 years |
Eurofins Lancaster Laboratories PSS is searching for a Molecular Biologist Associate to work with Automation/High-Throughput technologies in San Diego, CA. | 06/25/2021 |
| 8472 | EAG Laboratories San Diego, CA Cell Culture Associate B.S. in Biology, Cell Biology, Molecular Biology, or related science. Exp: 1 year |
Eurofins is searching for a Cell Culture Associate to provide assistance in a cell culture laboratory to support protein expression and cell line generation. | 06/25/2021 |
| 8473 | EAG Laboratories San Diego, CA Analytical Chemist: Entry Level Bachelor's degree in Analytical Chemistry, Biochemistry, Pharmaceutical Science or related discipline. Exp: 1-5 years |
Develop, qualify and validate analytical test methods for drug product, intermediates and excipients Design and execute analytical development studies Write analytical method validation protocols and reports Write and maintain applicable SOPs Provide analytical support to QC, Process Engineering and Manufacturing as applicable Perform externally generated data review Assist in development stability study design and protocol writing Assist management during regulatory inspections and internal audits | 06/25/2021 |
| 8474 | Amicus Therapeutics Philadelphia, PA Research Associate BS Exp: 0- 2 years’ |
Amicus Therapeutics is a global, patient-dedicated biotechnology company focused on discovering, developing and delivering high-quality medicines for people living with rare metabolic diseases. The successful candidate will be highly motivated individual ready to work within a science-focused, collaborative, multidisciplinary drug discovery and development environment. The Associate Scientist will be responsible for supporting lab operations in upstream and downstream protein production, viral vector production, and assay support. | 06/13/2021 |
| 8475 | Amneal Pharmaceuticals Brookhaven, NY Scientist I, Quality Control - (210EA) Bachelors Degree (BA/BS): Chemistry or related field - Required Exp: Less than one year |
The Scientist I - Quality Control is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 6/13/2021 |
| 8476 | Amneal Pharmaceuticals Brookhaven, NY Scientist I, Quality Control - 2nd Shift - (210EB) Bachelors Degree (BA/BS): Chemistry or related field - Required Exp: Less than one year |
The Scientist I - Quality Control is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 6/13/2021 |
| 8477 | Amneal Pharmaceuticals Piscataway, NJ Scientist II, Quality Control - (200KO) Master Degree (MBA) Chemistry or related science discipline - Preferred Exp: 1 year + |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 06/13/2021 |
| 8478 | Amneal Pharmaceuticals Bridgewater, NJ Scientist II, AR & D - (210DV) Master Degree (MS/MA): Chemistry or related science - Preferred Exp: 1 year + |
The Scientist 2 is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. The individual in this capacity performs analytical methods qualifications/validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods and maintains/qualifies analytical equipment. | 06/13/2021 |
| 8479 | Amunix South San Francisco, CA Lab Technician B.S. in Chemistry or Biology or similar scientific discipline. Exp: 1-2 years |
The Lab Tech is responsible for supporting routine operations of the Fermentation and Purification Labs and completing routine laboratory procedures under the direction of the BioProcess Development and Manufacturing Lead. | 06/13/2021 |
| 8480 | Amunix South San Francisco, CA Research Associate, Protein Analytics Masters or Bachelor degree in analytical chemistry, protein chemistry, biochemistry, pharmaceutical sciences or relevant scientific discipline. Exp: 0-3 years |
Amunix is seeking a Research Associate to join the analytical group to support analytical method development and quality control activities for Amunix’s pipeline. The candidate must have a strong initiative and desire to work in a fast paced, team-oriented, dynamic environment. | 06/13/2021 |
| 8481 | AnaptysBio San Diego, CA Research Associate I Bachelor’s degree in Molecular Biology or related scientific field. Exp: 0-2 years |
This position is responsible for the processing and preparation of samples to generate libraries for next generation sequencing, and possibly participate in other molecular biology activities such as cloning of antigens, antibodies and their mutational variants. | 06/14/2021 |
| 8482 | AnaSpec Fremont, CA Research Associate - Biology B.S in Biochemistry, Chemistry, or related discipline. Exp: 0-3 years |
Perform assay kit production and QC tests: enzyme activity assays, protein expression, purification. Manage orders, maintain inventory. Perform protein labelling and conjugation procedures. Prepare product datasheets, SOPs. Manage routine activities, including meticulous record keeping. Participation in R&D projects expected. Ensure implementation, compliance, and continuous improvement of QMS through SOP documentation. Other duties as assigned by Management. | 06/14/2021 |
| 8483 | Antibodies Inc Davis, CA Research Associate Antibody Development BS in life sciences. Exp: 1-3 years |
We are currently seeking a research-associate to join our growing antibody development group. The ideal candidate will have hands-on experience with mammalian cell culture and with antibody-based assays (Western Blot, ELISA, Immunocytochemistry, Immunohistochemistry, etc.). Additional experience in molecular biology and protein purification would also be an asset but is not required for this position. | 06/15/2021 |
| 8484 | Antibody Solutions Santa Clara, CA Research Associate I - Immunochemistry (santa clara) Level I requires a Bachelor's Degree. Exp: 0-2 years |
Responsibilities include running immunochemistry assays (i.e. ELISA, Flow Cytometry) including all reagent and buffer preparation, assay design, and varied techniques. | 06/15/2021 |
| 8485 | Arraystar Rockville , MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 06/16/2021 |
| 8486 | ArunA Biomedical Athens, GA Quality Control/ Analytical Development Associate I Bachelor’s degree in a biomedical science. Exp: 0-2 years |
We are looking for an energetic, highly motivated individual who wants to work in a fast-paced, team-focused environment, within our Quality and Analytical Development Group. This individual will perform testing to support manufacturing, development and characterization efforts for our exosome products, reporting into a QC supervisor or manager. Activities include conducting a variety of cellular, molecular biology and analytical tests on raw materials, process intermediates, drug substance, drug product and stability samples. | 06/16/2021 |
| 8487 | Aspen Neuroscience San Diego, CA Quality Control Technician BS degree or higher in cellular or molecular biology, chemistry, physics or engineering (e.g. biochemical). Exp: 1-2+ years |
The Quality Control Technician, Cell Therapy Development, will report to the Senior Quality Control Scientist. This position will support assay development and stem cell therapy manufacturing and release testing related to induced pluripotent stem cell (iPSC) derived dopaminergic progenitor cells of a first-in-human clinical trial for the treatment of Parkinson’s Disease. | 06/16/2021 |
| 8488 | Atalanta Therapeutics Boston, MA Associate Scientist II / Senior Associate Scientist – siRNA Screening (2 Positions Available). Master’s degree in biochemistry or relevant biological science . Exp: 0-5 plus years |
Atalanta Therapeutics is seeking an experienced and highly motivated Associate Scientist II / Senior Associate Scientist to be part of the dynamic and collaborative In Vitro Biology team. This individual will contribute to cell-based screening of therapeutic oligonucleotides under direction of the HTS lab head. S/he will be responsible for routine cell line maintenance, optimization of medium to high-throughput cellular assays to quantitate mRNA or protein marker levels, and execution of siRNA efficacy screens to support preclinical drug development for multiple therapeutic targets. The Associate Scientist II / Senior Associate Scientist will be flexible to changing priorities/timelines and have strong attention to detail, organization and communication skills. | 06/16/2021 |
| 8489 | Atreca San Carlos, CA RESEARCH ASSOCIATE I/II, CELL BIOLOGY/FACS (TEMPORARY) B.S. or M.S. in biology or related discipline. Exp: 0-5 years |
The Temporary Research Associate I/ II will utilize his/her cell biology and flow cytometry skills to isolate immune cells and sort them into microplates in a biosafety level 2 (BSL2) environment. He/ She will also be utilizing in vitro assays to characterize antibodies. This position will work in a collaborative team environment. The successful candidate will be detail-oriented and patient in working with our delicate cell sorting machines. There will be opportunity for permanent employment based on performance. | 06/16/2021 |
| 8490 | Avantor Sciences Paris, KY QC Lab Analyst Bachelor’s degree in a natural/life science discipline. Exp: 0-2 years |
Under the direction of the Quality Control Supervisor; responsible for working within the approved safety guidelines to test samples; responsible for chemical and/or physical analysis activities of high complexity on raw materials, in process and finished products. Prepare solutions and control results, materials and reagents. Ability to recognize and identify problems while using technical resources; basic knowledge and use of SAP and Master Control is necessary at this job level. | 06/16/2021 |
| 8491 | Be Biopharma Kendall Square, MA Research Associate / Sr Research Associate Master’s Exp: 1+ years |
Help to establish protocols around differentiation of primary immune cells, including extensive tissue culture work (maintenance, expansion, and banking) Handling and analyzing workflows pertaining to cellular differentiation and profiling with downstream qRT-PCR, protein quantification, and other molecular readouts Cloning of constructs to support cellular engineering efforts Detailed record-keeping and protocol refinement as related to molecular and cellular assays Facilitate efficient transfer of assays to CRO partners where applicable | 06/17/2021 |
| 8492 | Beckman Coulter Diagnostics [Danaher] SE Bothell, WA Associate Scientist, Chemistry R&D M.S degree in Chemistry or Biochemistry or similar science. Exp: 0-2 years |
This individual will be primarily responsible for performing a variety of oligonucleotide purifications to support early phase assay development teams achieve key milestones leading to design lock and eventual product commercialization. This individual will have cursorily operational competence of the MerMade and Shasta Synthesizer platforms. Additionally, the individual will have expert knowledge of Agilent analytical HPLC systems to perform oligonucleotide purifications and characterization, as well as quantitation of oligonucleotides via UV/Vis analysis. Expert operational experience of Thermo LTQ-XL high throughput mass spectral analyzer with intermediate level skills in the interpretation of the resultant spectra is expected. The Associate Scientist will support a variety of innovation teams and scientists within Bothell for multiple sub-projects that require specialty chemical skills. Post synthetic modification of oligonucleotides and characterization / analytical testing of complex biomaterials will be required. The individual will be hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment. Also, this individual will be responsible for training junior personnel how to prepare modified DNA and perform purifications of complex oligonucleotide designs, as well as assist with process transfer to our oligonucleotide development team. | 06/17/2021 |
| 8493 | Beckman Coulter Diagnostics [Danaher] Sunnyvale , CA Clinical Research Associate I Bachelor's degree in a scientific field (Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology), RN or BSN Exp: 0-2 years |
Review on-site files, product accountability logs, study supplies inventory, case report forms, and source documents for completeness, accuracy, consistency and compliance; identifies deficiencies and discrepancies and provides remedial training and/or corrective action as the need arises. Provide site support for remote/electronic data capture (EDC), review for completeness and consistency, and generate and resolve queries in between monitoring visits. Responsible for timely identification of problems or issues that could affect the results or timely completion of the trial, or any protocol deviations, and for suggesting mechanisms for solving the problem. Completion of monitoring reports and follow-up letters, which includes providing summaries of significant findings, deviations, deficiencies and recommended action to secure compliance. Ensure that studies adhere to FDA regulations, Good Clinical Practices, and IVD directives. | 06/17/2021 |
| 8494 | Beckman Coulter Diagnostics [Danaher] Sunnyvale , CA Research Associate BS in relevant field - e.g. Molecular Biology, Biochemistry, Bioengineering, Chemistry, Biology, Genetics or related field. Exp: 0- 2 years |
This position is part of the FIT (Fast Impact Team) in the Biotechnology R8D Department. The Research Associate is an entry-level bench scientist focusing on real time PCR and RT-PCR assay and product development in an FDA-QSR and ISO9001 compliant organization. The FIT Program objective is to dedicate highly skilled cross-functional teams to product Sustaining and product Enhancement projects. R&D FIT will support 2-4 prioritized projects simultaneously based on customer and/or business impact. Requirements include proficiency in PCR, qPCR, RT-qPCR, knowledge of nucleic acids, enzymes and sample types (e.g. blood, plasma, FFPE, and urine), and familiarity in experimental design and laboratory practices. In addition to technical qualifications, the ideal candidate will be highly goal-oriented, inquisitive, organized, and be able to thrive in an atmosphere of shifting demands and priorities. The candidate should possess excellent oral and written communication skills. The ability to work in a cross-functional team-based environment is a must. | 06/17/2021 |
| 8495 | Beckman Coulter Diagnostics [Danaher] SE Bothell, WA Analytical Chemist B.S. Degree in Chemistry or a similar discipline. Exp: 0-2 years |
The Analytical Chemist will perform testing of compounds from small molecules, such as Cepheid proprietary chemical reagents, to synthetic oligonucleotides for use in Cepheid in-vitro diagnostic products. The test methods involve the operation of a variety of analytical equipment, including but not limited to HPLC, LCMS, and UV-Vis Spectrophotometers. | 06/17/2021 |
| 8496 | Beckman Coulter Diagnostics [Danaher] Lodi, California, United States of , CA Reagent Production Associate (3 locations) Bachelor’s Degree in Life Sciences. Exp: 0-2 years |
Responsible for supporting the Formualtion Specialist I production laboratories by following good documentation practices (cGDP) and relevant standard operating procedures (SOPs). Complete assigned tasks and ensure all activities are compliant with the company’s quality, safety and departmental policies and standards. Apply analytical skills or scientific methods or operational processes to perform release testing utilizing the GeneXpert system with guidance and direction from others. | 06/17/2021 |
| 8497 | BioAssay Systems Hayward, CA Research Associate - Assay Development A bachelors degree in biochemistry, chemistry, biology, or related field. Exp: 1-2 years |
We currently have an exciting opportunity for an enthusiastic research associate to join our growing R&D team. This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers. This is a fantastic opportunity for a motivated recent graduate to be part of a successful and expanding team while learning a number of laboratory skills in a supportive environment. In addition, working on service projects will expose the candidate to multiple other companies and research areas. Moreover, as a small company we offer ample opportunities for professional growth and faster than average promotions. | 06/17/2021 |
| 8498 | BioAssay Systems Hayward, CA Research Associate - Manufacturing A college degree in chemistry, biochemistry or biology. Exp: 1-2 years |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing, and packaging the finished products. This candidate may also join part time in our R&D team. | 06/17/2021 |
| 8499 | BioFire Diagnostics [Biomerieux] Salt Lake City, UT Research Associate B.S. in chemistry, biology, or a related field. Exp: 0-1 years |
The Template Control Research Associate (RA) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The RA-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. The RA-I will receive general instruction on routine work, perform lab duties with minimal supervision, and receive training and additional instruction for new tasks as needed. Substantial preference will be given to candidates who hold a B.S. in chemistry, biology, or a related field, but exceptional applicants with an Associate’s degree will be given consideration. Strong pipetting skills, attention to detail and organization, and familiarity with Excel and Word are required. Previous lab experience is desired, and familiarity with bioinformatics programs and cGMP compliance is a plus. | 06/17/2021 |
| 8500 | BioFire Diagnostics [Biomerieux] Salt Lake City, UT Research Associate I Bachelor’sdegree in a scientific discipline. Exp: 0-2 years |
Come be a part of our team and our mission as a Research Associate! This is a full time non-exempt position. This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. This person works closely with other research associates in the department. Performs general lab duties, designs and conducts experiments, collects and analyzes data, and keeps an accurate record of all work done in accordance with the quality system. Requires some problem solving skills. Normally receives general instructions on routine work, detailed instruction on new assignments. Reports to the Senior Research Associate or Scientist. | 06/17/2021 |
| 8501 | BioFluidica San Diego, CA Research Assistant, Full Time BS in biological or Bioengineering sciences. Exp: 1+ years |
The RA will be responsible for supporting scientific staff in daily processing samples. This person will also participate in execution and optimization of current protocols in the commercial development team. The RA will aid the other laboratory functions such as reagent preparation, cell staining, cell isolation and general laboratory technical support. The successful candidate must be willing to take on new responsibilities and vary work schedule to accommodate company needs, this may require occasional long work days. | 06/17/2021 |
| 8502 | BioReliance Madison, WI Associate Scientist Bachelors Degree in Chemistry, BioChemistry or related sciences. Exp: <1 year |
The Associate Scientist is responsible for the analysis of samples from Process and Analytical Development (PAD), related paperwork, troubleshooting analysis issues, and general laboratory tasks. Analysis involves the use of HPLC, GC, DSC, TGA, IR, MS, NMR and XRPD, among other instrumentation, along with wet chemical assays. The Associate Scientist is responsible for transferring and evaluation of analysis techniques used to release starting materials, intermediates, and final products as well as in‑process controls. The Associate Scientist may be responsible for developing analytical methods to support Development for eventual validation. | 06/17/2021 |
| 8503 | BioReliance Lenexa, KS Associate Scientist Quality Control Bachelor’s Degree in Microbiology, Biology, Biochemistry, or related Life Science. Exp: 1+ years |
The Associate Scientist – Quality control at MilliporeSigma will be responsible for performing Quality Control microbiology activities in support of GMP products, including routine testing and peer review of raw materials and finished products. | 06/17/2021 |
| 8504 | BioReliance Burlington, MA Associate Scientist Downstream Master’s Degree in Chemical Engineering, Biotechnology, or related Life Science/Engineering discipline. Exp: 1 year |
MilliporeSigma in Burlington, MA is searching for an Associate Scientist with Downstream Processing experience to join our Biodevelopment Process Development group (E2E) team. The successful candidate will be primarily responsible for generating material as well as developing purification processes for a variety of therapeutic candidate proteins such as monoclonal antibodies, bispecific and Fc fusion proteins. Scope of work will include, but is not limited to, protein purification, biochemical and biophysical characterization of proteins, novel purification technologies, process development, data analysis and project reporting. The individual will be responsible for execution of client project according to budget and timelines given to the project team. | 06/17/2021 |
| 8505 | BioReliance Billerica, MA Associate Scientist, Medicinal Chemistry Bachelor’s degree in Chemistry, Chemical Engineering, or other Scientific discipline. Exp: <1 year |
At EMD Serono, the Associate Scientist – Medicinal Chemistry will contribute to the achievement of drug discovery project goals through the synthesis of target molecules by applying modern organic synthetic methods and following best medicinal chemistry practices. | 06/17/2021 |
| 8506 | BioReliance Temecula, CA Associate Scientist Bachelor’s degree in Life Sciences discipline. Exp: 1+ year |
Work as part of the antibody development team for MilliporeSigma to produce new products, technologies and services that allow scientists to carry out their research in the most accurate, robust, reproducible, and expedited way possible. Team with technology transfer, marketing, manufacturing sciences, and quality departments to successfully transfer new products into manufacturing. In this role you will Learn new techniques, processes, and laboratory methods. Develop by on-the-job training, attending seminars, and reading literature. Present research results and product development efforts internally via reports and presentations. Contribute to marketing materials as needed. Learn new techniques, processes, and laboratory methods. Develop by on-the-job training, attending seminars, and reading literature. Present research results and product development efforts internally via reports and presentations. Contribute to marketing materials as needed. | 06/17/2021 |
| 8507 | Bio-Techne Minneapolis, MN Research Associate Bachelors or Masters degree in biochemistry or equivalent. Exp: 0 to 2 years |
The responsibilities of this position is to purify proteins for restock and modify existing protocols to meet the demand of our customers. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of existing products to help advance Bio-Techne's evolving portfolio. | 06/17/2021 |
| 8508 | Bio-Techne Woburn, MA Process Engineering Associate BS or MS in Chemical Engineering, Polymer Science, Materials Science or related discipline. Exp: 1-3 years |
As part of an interdisciplinary team, this position will support development and troubleshooting of novel polymeric reagents for cell and gene therapy research and clinical use. The role will focus on formulating new hydrogel microspheres to deliver scalable, repeatable and functional product for a variety of internal and external customer projects. Additionally, the Product Engineer will contribute to developing new chemical, imaging and cell based analytical tools with opportunity to collaborate with technical groups across Bio-Techne. You’ll join a strong and fun team of biologists, chemists and engineers focused on developing next generation tools for immunotherapies and research, with great opportunities to develop your technical and intellectual skill sets in a highly dynamic and interactive environment. We are looking for an individual who is highly motivated, organized, with a positive can-do attitude, and the flexibility to support a variety of company activities and projects, such as lab management and product manufacturing. Prior polymer science or materials engineering experience research experience is desirable. | 06/17/2021 |
| 8509 | Bio-Techne Minneapolis, MN Research Associate, Cell Culture and Stem Cell Media Operations and Support Services Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small and large scale cell culture to produce antibodies grown in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions, media and supplement preparation, and additional duties as assigned. This position requires a Tuesday through Saturday workweek. | 06/18/2021 |
| 8510 | Bio-Techne Newark, CA Research Associate, PAS B.S. or M.S. in life sciences and/or in molecular biology, biochemistry, cell biology or related field. Exp: 1-2 years |
This position will serve as key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic clients. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. The Research Associate must be willing to learn new techniques quickly and be able to adapt to shifting priorities in a fast-paced and growing start-up environment. This position will be based in Newark, California. | 06/18/2021 |
| 8511 | Catalent Morrisville, NC Associate Scientist Bachelor’s Degree in chemistry or closely related physical science. Exp: 1-3 years |
The Research Triangle Park (RTP) facility is Catalent's Center of Excellence for Analytical Services and is also home to Catalent's Inhalation franchise including product development, clinical and commercial manufacturing for pMDI, DPI and Nasal Sprays. | 06/18/2021 |
| 8512 | Catalent Winchester, KY Microbiologist, 2nd Shift Bachelors Degree in Microbiology, Biology or Chemistry (Preferred in Microbiology or Biology). Exp: 0 to 5 years |
The Microbiologist is primarily responsible for performing complex, non-routine microbiological analyses, and therefore must be capable of recognizing the need for pathogen identification, solving microbiological system problems, and leading and completing microbial investigations related to the water system, environmental monitoring of production equipment and the air handling system. The work is “hands on” and maintains the microbial testing needed to support raw materials, finished goods and environmental monitoring for the facility. | 06/18/2021 |
| 8513 | Catalent Webster, TX Manufacturing Associate I (Cell Therapy) B.S degree in biochemistry, chemical engineering, bioengineering, or related technical field. Exp: 0 - 2 years |
The Manufacturing Associate I (Cell Therapy) is responsible for supporting the overall GMP manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of cell therapy production and/or human cells cultivation. The Manufacturing Associate I (Cell Therapy) role is critical to our patients. Manufacturing life-saving medicines right the first time for themselves and their team with patient safety in mind is our priority. Quality, safety and on-time delivery is a must to be successful in this role! | 06/18/2021 |
| 8514 | 10X Genomics Pleasanton, CA Research Associate - Sequencing Core Bachelor Science degree in Biology, Biochemistry or related discipline. Exp: 1-3 years |
We are seeking an experienced, collaborative and adaptable individual to join our 10X sequencing core team. The candidate will have a strong background in nucleic acid quantification and NGS workflows. Ideally this candidate will also have an understanding of Illumina NGS or other sequencing experience. Individuals applying for this position must be self-starters, flexible in changing direction and methods, thrive in a fast paced, high throughput environment, excel at managing multiple priorities, able to effectively communicate with all levels within the organization and have the prior work experience needed to quickly learn the protocols. | 6/7/2021 |
| 8515 | 23andMe Sunnyvale, CA Research Associate, Research Ethics Bachelor’s degree or Associate’s degree. Exp: 1-2 years |
23andMe is seeking a talented research associate to support the regulatory efforts of 23andMe’s Human Research Protection Program (HRPP). This person will join a team of Regulatory Scientists and will assist with the IRB submissions of research protocols, manage project-tracking systems, and contribute to compliance-related activities. This is an exciting opportunity to learn about the ethical and regulatory components of the personal genomics industry and take an active role in the protection of research participants who are contributing to ground-breaking genetics research. | 6/8/2021 |
| 8516 | 4D Molecular Therapeutics Emeryville, CA Research Associate - Contract B.S. degree in biology, bioengineering, or a related field. Exp: 1+ years |
4DMT is in need of a talented and motivated Research Associate (Contract) to join our R&D team in supporting our viral drug therapy research efforts as we contribute to the future of gene therapeutics. This position will combine modern molecular and cell biology methods to help streamline 4DMT’s proprietary discovery platform. This individual will work closely with the Discovery group, but is expected to be a collaborative team member within R&D. | 6/8/2021 |
| 8517 | 4D Molecular Therapeutics Emeryville, CA Research Associate, Analytical Development/Quality Control MS degree in Biochemistry, Biology, or related field. Exp: 1+ year |
The Research Associate in Analytical Development/Quality Control (ADQC) is responsible for performing routine analytical testing, data analysis, and method development/qualification. The candidate will work closely with Process Development, Research, and Quality organizations. The successful candidate will be experienced with analytical techniques including but not limited to qPCR/ddPCR, electrophoresis, ELISA, CE (CE-SDS, cIEF), and UV/VIS spectroscopy. | 06/08/2021 |
| 8518 | 4D Molecular Therapeutics Emeryville, CA Sr. Research Associate I, Cell-Based Potency Assays MS in bioprocessing, chemical engineering, biochemistry, or biology preferred. Exp: 0-4 years |
4DMT needs a motivated, detail-oriented, and experienced Sr. Research Associate I/II. This individual will join a growing Cell-Based Assay (CBA) team to develop, optimize and validate cell-based bioassays for the characterization, lot release/stability testing and formulation assessment of AAV-based gene therapy drug substances and drug products. Sr. Research Associate I/II will interface with Research, Discovery, Process Development, Manufacturing, Quality, and Facilities functional groups as well as external parties (CRO, CDMO) to support life cycle of bioassays for current and new candidates during early- and late-stage GMP production. This is a CMC position, and the level will be determined based on the candidate’s experience and qualifications. | 06/08/2021 |
| 8519 | Abbott St Paul, MN Quality Engineer I BS degree in Engineering or Technical Field. Exp: 0-3 years |
Non-Conforming Material Reports (NCMR) including; root cause investigation, risk assessment, historical record review, disposition strategy, correction activities. Complaints Reviews/Manufacturing Analysis/Field Impact Escalation including; event assessment, root cause investigation, risk assessment, historical record review, impact/action escalation. Corrective Action Preventive (CAPA); including root cause investigation, scoping/bracketing, resolution planning, implementation, and verification of effectiveness. Regulatory requests including; certification of compliance and product inquires. Manufacturing/Production Line Support – partnering with operations team members to achieve value stream goals and objectives. Change Control – lead documentation change orders per quality system requirements using PLM system. Validation/Qualification – Lead/review Installation Qualification, Process Qualification, Operational Qualification, Product Performance Qualification (PPQ), Master Validation Plan/Report, and Test/Inspection Method Validation. Risk Management – use and interpret Hazard Analysis, use/update/create Failure modes and Effects Analysis. Support backroom during audits. Line Reviews – supports timely completion of manufacturing front line personnel reviews. | 06/08/2021 |
| 8520 | Abbott Abbott Park, IL Electrical Engineer Bachelor’s degree in the areas of Electrical/electronic engineering or related engineering field. Exp: six months |
This position performs entry-level activities which will include 70% time in lab troubleshooting PCB, cables, using scopes, and other diagnostic tools. Willing to perform runs on the system multiple days in a row. Solve problems independently. Applies a high level of technical support in a specialized discipline using knowledge and theory of electronics; life science; chemistry; mechanics; software; etc. Understands and uses knowledge of other disciplines. Uses computer applications as needed for functional specialty. Advanced skills in computer hardware and /or software applications. Document lab activities and troubleshooting. Accepts non-routine and complex assignments. Follows established procedures Uses judgment and makes choices on how to proceed. Assignments often require creativity. Researches; recommends; and implements appropriate changes for process improvements. Uses information from within and/or outside the organization when necessary. Reads; understands and instructs others in the use of manuals; test procedures; and documentation associated with specialized equipment. Reads; interprets; and may create engineering drawings; schematics, and complex test procedures. Writes basic procedures and technical documents. Working knowledge and use of complex tools and equipment specific to functional areas. May use statistical; mathematical and other quantitative and qualitative methods and measurements. Additional time may include design and develop, construction, and evaluation of a variety of prototype Printed Circuit Boards, fixtures, and tools. Promotes the process of continuous quality improvement and risk management and coordinates solutions for technical and project issues. Applies engineering and scientific principles to the evaluation and solution of technical problems. Exercises independent judgment in planning and organizing work; monitors performance and reports status. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. | 06/08/2021 |
| 8521 | Absci Vancouver, WA Research Associate, Analytical Development BS in Analytical Chemistry, Biochemistry, Molecular Biology, Bioengineering or related scientific discipline. Exp: 1-2 years |
We are currently seeking Research Associates to join our growing Analytical Development group! Using your adept problem-solving skills, you will play a significant role in analytical method development and characterization of therapeutic proteins expressed using SoluPro™, AbSci’s proprietary E. coli expression platform. You will demonstrate high attention to detail, the ability to learn new skills, to work both independently and collaboratively, and be comfortable thriving in a dynamic startup environment where research targets change from day to day. | 06/08/2021 |
| 8522 | Absci Vancouver, WA Research Associate, High-Throughput Screening - Cell Culture/Strain Banking Bachelor's Degree in Microbiology, Biochemistry or related field. Exp: 1 - 2 years |
As a Research Associate on the High-Throughput Screening team your primary focus will be culturing genetic variants to generate material for a variety of proprietary high throughput assays. You are enthusiastic about laboratory bench work, have meticulous attention to detail, an eagerness to learn new techniques, and are comfortable working in a highly dynamic and rapidly scaling company. While work will initially be 100% E.coli based, there is the potential to expand that into mammalian cultures in the future. After training, this role will be required to work 1 set weekend day per week as part of a regular (5 day) schedule. | 06/08/2021 |
| 8523 | Absci Vancouver, WA Research Associate/Sr. Research Associate - Cloning Master’s degree in Molecular Biology, Biochemistry, Microbiology, or a related discipline. Exp: 1-2 years |
The Research Associate/Sr. Research Associate, under direction of the Molecular Sciences team, will support innovative experimental research that advances AbSci’s proprietary E. coli SoluPro® expression platform. Primary responsibilities include providing core support to ongoing DNA construction, strain engineering, and NGS sequencing activities. The ideal candidate will demonstrate rapid mastery of assigned tasks and the capacity to take on additional technical responsibilities within an expanding team. | 06/08/2021 |
| 8524 | Absci Vancouver, WA Research Associate I/II - Purification Bachelor’s degree in Biochemistry, Molecular Biology, Bioengineering or related scientific discipline. Exp: 1-2 years |
We are currently seeking Research Associates to join our growing purification team! Using your adept problem-solving skills, you will play a significant role in downstream process development and analytical testing of therapeutic proteins expressed using SoluPro™, AbSci’s proprietary E. coli expression platform. You will demonstrate high attention to detail, the ability to learn new skills, to work both independently and collaboratively, and be comfortable thriving in a dynamic startup environment where research targets change from day to day. | 06/08/2021 |
| 8525 | Absorption Systems Medford, MA Research Associate I BS in a scientific field. Exp: 0-3 years |
The Research Associate I will work as part of a team in a lab environment to complete client-driven projects. | 06/08/2021 |
| 8526 | Acepodia San Francisco Bay Area, CA Research Associate/Senior Research Associate MS degree. Exp: 1+ year |
We have an exciting opportunity for motivated individuals to join our R&D team working to develop cell therapies against cancer. The successful candidate will be expected to be a good team player, work with enthusiasm to execute assignments properly. | 06/08/2021 |
| 8527 | ACI Clinical [WCG Careers] Washington, DC Research Assistant BA or BS with some coursework in a natural science (e.g., biology, chemistry, or physics) or experimental psychology. Exp: 0-2 years |
Our Research Assistants are integral parts of teams. They support projects for clinical trials involving new drugs, biologics, devices, and vaccines, as well as behavioral interventions across a range of disease areas. A Research Assistant who is successful at Statistics Collaborative is a project team member who develops a deep understanding of the clinical trial and our responsibilities related to that trial, and who has the ability to take on more responsibility within and across projects. This is an entry-level position (0-2 years of experience) with opportunity for growth. | 06/08/2021 |
| 8528 | Adare Pharmaceuticals Vandalia, OH Analytical Scientist I BS or MS degree in Chemistry or equivalent degree in physical sciences is expected. Exp: entry level |
The essential job function is to support the development and validation of analytical methods for raw materials, work-in-process, and finished products and to provide testing support for the formulation development and clinical supplies release process. | 06/08/2021 |
| 8529 | Adare Pharmaceuticals Vandalia, OH QC Analyst A Bachelor degree in Chemistry or related field. Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. This position works 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, work Saturday and Sunday then off Monday and Tuesday, etc. | 06/08/2021 |
| 8530 | Adare Pharmaceuticals Vandalia, OH QC Analyst A Bachelor degree in Chemistry or related field. Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. This position works 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday etc. | 06/08/2021 |
| 8531 | Adare Pharmaceuticals Vandalia, OH Raw Materials Chemist A Bachelor degree in Chemistry or related field. Exp: 1 to 3 years |
The essential job function is to perform physical and chemical testing of raw materials in accordance with written procedures and compendia guidelines as well as manage the paperwork associated with the control and management of raw materials. | 06/08/2021 |
| 8532 | Adimab Lebanon, NH Research Associate - Mass Spectrometry B.S. in analytical chemistry, biochemistry, or related fields. Exp: 0-2 years |
We are seeking an eager-learning worker with a background in biochemistry, biophysics, analytical chemistry or related concentrations to join our Protein Analytics team. The Research Associate will work in a small team setting to support Adimab’s novel antibody discovery, optimization, and characterization workflows. This role will closely interface with the Antibody Engineering, Antibody Sciences, High-Throughput Expression, and Molecular Core teams. | 06/09/2021 |
| 8533 | ADMA Biologics Boca Raton, FL QC Lab Support Associate I Requires a Bachelor’s degree in Biology, Chemistry, Medical Technology, or related scientific field. Exp: 1-3 years |
The QC Lab Support Associate I will Perform cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. Performs all work under GMP conditions. Provide customer support to QC analysts. | 06/09/2021 |
| 8534 | ADMA Biologics Boca Raton, FL Chemist I B.S. in Chemistry, Biochemistry, Molecular Biology or related science discipline. Exp: 0-3 years |
The Chemist I will Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. | 06/09/2021 |
| 8535 | Akoya Biosciences Menlo Park, CA Research Associate Bachelors or Masters in Life Sciences with experience in a laboratory/pathology environment. Exp: 1-2 years |
Akoya Biosciences is seeking an entry level Research associate to join our Reagents team in Menlo Park, CA. The successful candidate will join a dynamic, team-oriented environment and take part in screening of new antibodies in the CODEX platform. The desired skillset for laboratory work includes the ability to perform immunohistochemistry (IHC) procedures. | 06/09/2021 |
| 8536 | Akoya Biosciences Menlo Park, CA Research Associate Requires a Bachelors or Master’s degree in Life Sciences with experience in a laboratory/pathology environment. Exp: 1-2 years |
Akoya Biosciences is seeking an entry level Research Associate to join our Reagents team in Menlo Park, CA. The successful candidate will join a dynamic, team-oriented environment and take part in screening of new antibodies in the CODEX platform. The desired skillset for laboratory work includes the ability to perform immunohistochemistry (IHC) procedures. | 06/09/2021 |
| 8537 | Akron Biotechnology Sarasota, FL Tech, Lab - Process Development BS in a life science concentration. Exp: 1-2 years |
Provide scientific insight and hands on technical laboratory techniques. Coordinate laboratory operations, workloads and projects tasks. Provide scientific and technical support, prepare written scientific reports. Execute bioassays and assist in the development of new bioassays. Participate in ongoing process development activities as directed. Perform general laboratory and instrumentation maintenance. Participates in the design and execution of investigations and experiments associated with product development Follow through with experiments and investigations by demonstrating discipline resourcefulness and willingness to follow procedures and guidelines. | 06/09/2021 |
| 8538 | Akron Biotechnology Sarasota, FL Tech, Laboratory BS in a life science concentration. Exp: 1-2 years |
Provide scientific insight and hands on technical laboratory techniques. Coordinate laboratory operations, workloads and projects tasks. Provide scientific and technical support, prepare written scientific reports. Execute bioassays and assist in the development of new bioassays. Participate in ongoing research efforts. Maintain laboratory notebook in compliance with good documentation practices. Perform in-house quality control testing of products Perform general laboratory and instrumentation maintenance. Participates in the design and execution of investigations and experiments associated with product development Follow through with experiments and investigations by demonstrating discipline resourcefulness and willingness to follow procedures and guidelines. | 06/09/2021 |
| 8539 | Alcami Charleston, SC Assistant Scientist - Microbiology Bachelor’s degree in Chemistry, Biology, Microbiology or a related field with course work in Microbiology. Exp: 0 – 2 + years |
The Assistant Scientist I is accountable for driving results in a fast-paced environment by performing routine microbial analyses, focuses on a few assays until proficient. The Assistant Scientist I may assist in GMP review. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 06/09/2021 |
| 8540 | Aldevron Madison, WI Quality Control Scientist I, Protein Bachelor’s degree in the field of chemistry, biochemistry, genetics, cell biology or related field. Exp: 1 year |
The Quality Control (QC) Scientist I, Protein, supports production of recombinant proteins. This role is primarily responsible for performing release testing and ensuring that products meet or exceed all quality specifications. This role also supports the management and execution of stability studies. | 06/09/2021 |
| 8541 | Aldevron Fargo, ND Biomanufacturing Operator II - Buffer Prep AS/BS degree in Chemistry preferred. Exp: 1 year + |
The Biomanufacturing Operator II will work daily within Aldevron’s labs performing tasks associated with Aldevron’s Research Grade (RG) services. The Biomanufacturing Operator II is expected to become familiar with all Aldevron products and to be able to perform most tasks associated with the production of plasmid DNA. | 06/09/2021 |
| 8542 | Aldevron Fargo, ND Laboratory Technician II - Technical Lead S. or B.S. degree in biology, chemistry, microbiology, or other life science degree preferred. Exp: 1-2 years |
The Laboratory Technician II Technical Lead oversees multiple projects simultaneously within the GMP and GMP-S area with a focus on first time right and patient first in full conformance with Quality and EHS requirements. This role assists the buffer preparation team and supervisors as directed, and fills in when supervisors are not available (eg. after hours, during PTO, and unplanned absences). | 06/09/2021 |
| 8543 | Aldevron Fargo, ND Laboratory Technician III - Technical Lead A.S. or B.S. degree in biology, chemistry, microbiology, or other life science degree preferred. Exp: 1-2 years |
The GMP Laboratory Technician Technical Lead oversees multiple projects simultaneously within the GMP buffer preparation area with a focus on first time right and patient first in full conformance with Quality and EHS requirements. This role assists the buffer preparation team and supervisors as directed, and fills in when supervisors are not available (eg. after hours, during PTO, and unplanned absences). | 06/09/2021 |
| 8544 | Alkahest San Carlos, CA Research Associate Proteomics Bachelor’s or Master’s degree in a field related to chemistry, biochemistry or biology. Exp: 1-year |
We are seeking a highly motivated Research Associate who will help advance our preclinical scientific activities to identify and characterize proteins associated with aging and disease. The role will primarily support proteomic analysis by state-of-the-art technologies including mass spectrometry and immunoassays. Studies performed will involve cutting edge science and require innovative concepts and strategies. The position is an excellent opportunity to engage in and learn a range of techniques in a dynamic environment and rapidly progress the company’s scientific activities. This role requires dedication to drive science, ability to multitask, excellent communication and organizational skills, attention to detail, and the ability to work independently as well as collaboratively with a multidisciplinary team of scientists and research associates in a fast-paced environment. Alkahest offers a competitive compensation and benefits package, annual bonus potential, opportunities for career growth and development, and a work environment that is collaborative, collegial and lots of fun. | 06/09/2021 |
| 8545 | Alkermes Wilmington, OH QA Associate I Bachelor’s degree in a scientific discipline or equivalent experience. Exp: 0-2 years’ |
The position will perform general QA work, using their ability as a skilled contributor in completing tasks where judgement is required in resolving problems and making recommendations. Works on problems of a diverse scope where analysis and problem solving is required. Receives general oversight and guidance on approaches to complete project related tasks. Applies job related skills and understanding of policies and standards in completing tasks. | 06/09/2021 |
| 8546 | Alkermes Wilmington, OH QA Associate I/II - Complaints Bachelor’s degree in a scientific discipline or equivalent. (QA I) Exp: 1 year(s) |
The position will perform general QA work, using their ability as a skilled contributor in completing tasks where judgement is required in resolving problems and making recommendations. Works on problems of a diverse scope where analysis and problem solving is required. Receives general oversight and guidance on approaches to complete project related tasks. Applies job related skills and understanding of policies and standards in completing tasks. | 06/09/2021 |
| 8547 | Allakos Redwood City, CA Research Associate I/ Research Associate II, Bioassay and Process Analytics Degree (BS, MS) in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific field. Exp: 0-1 year |
As a Research Associate, you will play a key role in supporting our ongoing product development. Responsibilities includes sample analysis using analytical methods which include, but are not limited to, SEC (size exclusion chromatography), CEX (cation exchange), CE (capillary electrophoresis) and plate-based assays such as residual DNA by qPCR and ELISA. You will have the opportunity to learn a broad range of analytical methods from molecular characterization to functional assessment. You will plan, execute, analyze and document the laboratory studies. The focus of the position is to work in the process analytics laboratory. | 06/09/2021 |
| 8548 | ALPCO Diagnostics Salem, NH Quality Control Analyst I BS in biology, biochemistry, or a related science. Exp: 1-3 years |
A successful candidate in this position will be able to multi-task and thrive in a high paced atmosphere. The Quality Control Analyst I is responsible for in-process component and final kit testing associated with ALPCO kits. This employee will develop familiarity with a variety of expectations, concepts, practices and procedures within the field as well as established laboratory concepts and practices. A Quality Control Analyst I performs a variety of tasks working under supervision. The Quality Control Analyst I reports to the Quality Control Supervisor. | 06/09/2021 |
| 8549 | ALPCO Diagnostics Salem, NH Quality Assurance Specialist I BS or MS degree. Exp: 0-3 years |
The Quality Assurance Specialist I will assist in the development, implementation, and coordination of product assurance programs to prevent or eliminate defects in new or existing products at ALPCO. This position will have responsibility for assuring that ALPCO Quality System requirements are effectively established, implemented, and maintained in compliance with cGMP and ISO 13485:2016 standards. The QA Specialist I will perform a variety of tasks working under direct supervision. The Quality Assurance Specialist I position reports to the Director of Quality & Regulatory. | 06/09/2021 |
| 8550 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 06/09/2021 |
| 8551 | Ambry Genetics Aliso Viejo, CA Quality Assurance Specialist I Bachelor of Science or related field. Exp: 1-3 years |
The Quality Assurance Specialist I support Ambry’s Quality Management System (QMS) and regulatory submissions. Responsible for processing requests, archival, filing, scanning, indexing and formatting new and existing documents within guidelines of the document control QMS procedures and the electronic document control system. Collate controlled documents and controlled records in support of regulatory submission requests, including but not limited to FDA and PMDA. Supports implementation of an electronic document control system. Possesses and applies a broad knowledge of Quality principles, practices, and procedures. Demonstrated knowledge of regulations, standards and licensure requirements, such as, clinical diagnostic laboratory standards: CAP and state licensures; Federal regulations CLIA and QMS; and Industry standards: ISO 13485 Medical Device QMS, ISO 14971 Risk Management Program, Software as a Medical Device and IEC 62304 Software Development Lifecycle. | 06/09/2021 |
| 8552 | Ambry Genetics Aliso Viejo, CA CLS I- RNA (Sun-Wed 10am-8:30pm) Bachelor's degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution or h Exp: 0-4 years |
The Clinical Laboratory Scientist (CLS) is responsible for following all standard operating procedures of the laboratory and adhering to all quality regulations. Additionally, the technologist may be assigned duties by the Lab Manager, Lab Supervisor, and other Clinical Laboratory Operations Leadership for the advancement or maintenance of the laboratory. | 06/10/2021 |
| 8553 | Ambys Medicines South San Francisco, CA Research Associate / Senior Research Associate, Cell Therapy BS or MS degree in a biological science discipline. Exp: 1-5+ years |
We are currently seeking a highly motivated Research Associate / Senior Research Associate with expertise in molecular and cell biology to join the Cell Therapy platform at Ambys. In this role, you will work as part of a multidisciplinary team to develop novel therapies to treat liver diseases using cell therapy and gene therapy strategies and will be in the pre-clinical Research group developing a proprietary human hepatocyte cell therapy. This is a lab-based role where you will be responsible for conducting experiments, collecting, managing, and analyzing experimental data, interpreting results, and preparing presentations for internal and external meetings and publications. You will be under direct scientific supervision of a scientist but should be highly organized and have the self-confidence to work independently in planned studies. You should enjoy working in a fast-paced dynamic team environment and be motivated to discover new breakthrough therapies for patients with severe liver disease. | 06/10/2021 |
| 8554 | Oncorus Andover, MA Associate Scientist II, HSV Process Development M.S. in Biochemistry, Chemical Engineering, Virology. Exp: 0-2 years |
We are looking for a highly motivated and innovative candidate for the role of Associate Scientist II, HSV Process Development. This is a fantastic opportunity to make a significant impact as a scientifically motivated self-starter capable of advancing key development projects. Projects will be primarily focused on downstream process development for our HSV-1 oncolytic virus platform. | 5/31/2021 |
| 8555 | Patheon (Thermo Fisher Scientific) Rockford, IL Quality Assurance Specialist I Bachelors degree required in a scientific discipline. Exp: 1 years |
Provide Quality Assurance Support to the Rockford site. Provide product and quality system information to internal and external customers. Review new paperwork and proposed changes for appropriateness and determine potential effects on product quality. Help strengthen our quality system and make improvements where needed. Help educate and promote adherence to Quality Assurance policies and requirements. Work with Quality Control in the review and development of specifications, test methods and protocols. | 6/2/2021 |
| 8556 | PCI Pharma Services Rockford, IL Microbiologist 1 Bachelor's Degree in a related field. Exp: 1-5 years |
The primary function of this role is to collect and process environmental samples from across all Rockford facilities using aseptic technique. In addition, this role is responsible for daily monitoring of the Laboratory temperature recorder charts for various equipment in the Laboratory. This role may participate in training of other analysis in techniques for which competency has been demonstrated. There are no supervisory responsibilities associated with this role. | 6/2/2021 |
| 8557 | PCI Pharma Services Rockford, IL QA Specialist 1 - Chemistry Lab Bachelor's Degree in a related field. Exp: 1-5 years |
This position is Primary function is the timely and efficient review ensuring accuracy, completeness and compliance to in--house, customer and regulatory requirement, including data integrity, are met following the testing of pharmaceutical starting materials, components and finished products using techniques such as manual/automated titrations, UV, FTIR, LOD, Karl Fisher, Water activity and Pharmacopoeial testing i.e. LOD, RI, ID, Limit tests, Training of personnel in data review in area of expertise. Author OOS investigations, determination of root cause and develop and implementation of corrective and preventative actions. Author investigations into deviations from defined procedures. Review of regulatory bodies for changes applicable to the laboratory and ensuring that any changes are implemented. Maintain metrics with respect to area of responsibility. There are no supervisory responsibilities. | 06/02/2021 |
| 8558 | PCI Pharma Services Rockford, IL Pharmaceutical Scientist 1 Bachelor's Degree in a related field. Exp: 1-5 years |
Primary function is to perform chemical and physical testing of pharmaceutical starting materials, components and finished products to client supplied and Pharmacopoeial methodology in accordance with regulatory standards with a high level of accuracy and minimal personal error. Testing is performed using techniques such as FTIR, UV and Karl Fisher with calibration, maintenance and troubleshooting of this equipment. Training of analysts in techniques for which competency has been demonstrated. Participation in OOS investigations and assisting in the determination of root cause. There are no supervisory responsibilities. | 06/02/2021 |
| 8559 | Pillar Biosciences Natick, MA Research Associate . B.S. or M.S in Biology, Molecular Biology, Genetics or related field. Exp: 1-3 years |
Performs under the direction of senior lab personnel; assists with and conducts laboratory experiments on research projects within well-defined guidelines, keeps abreast of current publications relative to methods, techniques and developments within area of research, evaluates results of process and summarizes data collected. | 06/02/2021 |
| 8560 | Pillar Biosciences Natick, MA Quality Control Technologist B.S. in Biology, Molecular Biology, Genetics or related field. Exp: 1 year |
Perform tasks supporting Quality Control activities in a highly regulated environment and in accordance with established standard operating procedures. | 06/02/2021 |
| 8561 | Pliant Therapeutics South San Francisco, CA Analytical Chemistry Research Associate MS in Organic Chemistry, Analytical Chemistry or closely related field. Exp: 0+ years |
The RA Analytical Chemist is responsible for daily analysis and processing of complex materials used to support multiple Pliant drug discovery programs. Position is full time and provides opportunity to use teamwork, innovation skills and advanced laboratory equipment to solve challenging chemical problems. The job will involve sample processing and method development using analytical HPLC, preparative HPLC, normal phase purification and LCMS, and will work closely with our medicinal chemistry, compound management and in vitro biology teams. | 06/02/2021 |
| 8562 | Precigen Germantown, MD Research Associate, Translational Immunology B.S. (0-3+ years) or M.S. (0+ years) in Immunology, Molecular Biology or related field. Exp: 0-3 years |
Based in our Germantown, Maryland office Precigen is seeking a Research Associate, Translational Immunology to support discovery and preclinical/translational research. We are seeking candidates with exceptional immunological research skills looking for a fast paced, exciting working environment utilizing state of the art technology. | 06/02/2021 |
| 8563 | Precision Biosciences Durham, NC Research Associate I, Next Generation Sequencing (NGS) BS degree in related field. Exp: 1+ years |
The Research Associate I, Next Generation Sequencing (NGS) is responsible for daily maintenance and operation of Core Technology’s next generation sequencers. They will perform standard library preparations with the use of liquid handling robots and assist team members with manual library preparation according to standard protocols. The incumbent will also be responsible for maintaining stock levels of standard sequencing supplies and reagents. | 06/02/2021 |
| 8564 | QurAlis Cambridge, MA Research Associate, Stem Cells A Bachelor’s degree in the biological sciences with 1+ year lab experience or master’s degree with 0-2 years lab experience. Exp: 1+ years |
QurAlis is seeking a highly motivated Research Associate to support and execute its cutting-edge discovery and screening efforts. The Research Associate will work closely with the QurAlis scientific and management teams to perform studies in a high quality and scientifically rigorous fashion. | 06/03/2021 |
| 8565 | Rakuten Medical San Diego, CA Research Associate III, In Vivo Pharmacology M.S. Exp: 1+ years |
Rakuten Medical is searching for a highly motivated individual to support Rakuten Medical’s preclinical in vivo pharmacology team. The candidate will design and execute studies to evaluate efficacy and mechanism of action of hit and lead candidate products utilizing the most appropriate in vivo pharmacology models. This individual will participate and present data at weekly research meetings, and interface with other key functions such as TechOps. The successful candidate is also expected to train other members of the multidisciplinary research team in scientific, technical, and operational aspects of in vivo pharmacology. In alignment with the Rakuten Medical company culture, the individual will be expected to perform these duties in a highly collaborative manner with other members of the multidisciplinary research team, and will also have the opportunity to learn and grow in other functions. | 06/03/2021 |
| 8566 | MannKind Danbury, CT Research Associate BS Degree in a chemistry or related science. Exp: 1-3 years |
Conducts sample analysis to support formulation and process development including HPLC, aerodynamic particle size distribution, moisture analysis. Characterizes physical and chemical properties including stability of prototype drug products. Assists with preparation and characterization of supplies for toxicology and early phase clinical studies. Writes reports and/or provides technical documentation. | 06/03/2021 |
| 8567 | Sebela Pharmaceuticals Holbrook, MA QC Chemist Minimum Bachelor’s degree in Chemistry, or related discipline. Exp: 0-2 years’ |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. | 06/03/2021 |
| 8568 | Selecta Biosciences Watertown, MA Research Associate, Quality Control A B.S. in Chemistry or related field or an M.S. Exp: 0-2 years |
Reporting to the head of the Analytical Testing and QC testing group, the Research Associate produces timely and accurate data and documentation for analyses targeting a variety of nanoparticle components such as small molecules, peptides, proteins, oligosaccharides and synthetic polymeric material in support of the development of preclinical and clinical products based on the company's proprietary synthetic nanoparticle technology developed to elicit the desired and optimal immune response. | 06/03/2021 |
| 8569 | Shine Medical Technologies Janesville, WI Mechanical Engineer - Nuclear Systems Bachelor’s degree in, Mechanical Engineering, Engineering Physics, Engineering Mechanics, or related discipline. Exp: 1+ years |
SHINE is immediately seeking a Mechanical Engineer to support the nuclear and mechanical systems in the Nuclear Systems Engineering Group, which ensure the safe, efficient, and effective design of the nuclear systems equipment. Key responsibilities include working with vendors to finalize design for fabrication, reviewing final design for installation and operability considerations, preparing or approving equipment test plans, participating in factory acceptance tests and site acceptance tests, performing site walkdowns, and other final design, procurement, installation, and testing tasks. | 06/03/2021 |
| 8570 | Sorrento Therapeutics San Diego, CA Research Associate (2 Openings) Bachelor’s Degree in Immunology, Molecular Biology or related disciplines with 1-2 years relevant experience or Master’s Degree with 0-2 years relevan Exp: 1-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking an experienced Research Associate. Responsible for the development and implementation of in vitro studies to support pre-clinical validation of CAR-T cellular therapies against cancer. The Research Associate has knowledge and hands on experience in cell culture, Flow cytometry and cell based assays. | 06/03/2021 |
| 8571 | Sorrento Therapeutics San Diego, CA Research Associate in Enzyme & DNA Production (5 Openings) Bachelor's Degree in Biology, Biochemistry or related disciplines. Exp: >1 years |
Sorrento Therapeutics (“Sorrento”) is looking for Research Associate to help with gene-editing enzyme production and DNA plasmid cGMP production including process development and manufacturing. Major tasks include: Buffer preparation, bacteria culture including fermentation and harvest, bacteria lysis and protein and plasmid DNA purification. | 06/03/2021 |
| 8572 | Sorrento Therapeutics San Diego, CA Research Associate/Scientist For RA Master's degree in Immunology, Molecular Biology or related disciplines. Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is currently looking for highly motivated individuals with extensive expertise in molecular and cellular Immunology to join group for next generation of CAR-T/DAR-T technology and product research and development including vector design, molecular cloning, CAR-T generation, and in vitro and in vivo functional assays of engineering T cells. | 06/03/2021 |
| 8573 | SQZ Biotech Watertown, MA Lab Technician Bachelor’s or Associate’s degree. Exp: one year |
SQZ Biotechnologies is seeking a Lab Technician to join our Operations team. Reporting directly to the Lab Operations Manager, the successful candidate will directly impact SQZ research by supporting inventory, equipment maintenance and supply chain management. The successful candidate should be highly motivated, take initiative and can think creatively to solve problems hands-on. This position will be integral for scale up processes for a fast-growing company. | 06/04/2021 |
| 8574 | Stemson Therapeutics San Diego, CA Research Associate - Cell Culture BS in cell biology, biochemistry, or related field; or an equivalent combination of education and experience. Exp: 1-year |
A Cell Culture Technician position is available at a visionary startup Stemson Therapeutics Corp. The candidate will report directly to the R&D Cell Culture Laboratory Manager and be part of a dynamic research and development team focused on hair follicle restoration using human induced pluripotent stem cells (iPSCs). We seek a passionate cell culture technician to assist us in accelerating the pace of our research by performing the critical tasks required for culturing large amounts of human and animal cells needed for hair follicle organoid generation, characterization, and testing. In addition to cell culture, the candidate will conduct characterization of the human and animal cells, the organoids, and hair follicles using a variety of analytical and biochemical techniques. | 06/04/2021 |
| 8575 | Synthorx [Sanofi] Meriden, CT Quality Control Technician - Vaccine Bachelor's degree required, preferably in one of the following fields of study: Biochemistry, Chemistry, Biology, Molecular Biology, Immunology, or th Exp: one year |
This position supports execution of routine testing in the Quality Control laboratory while strictly adhering to site work instructions, and procedures. This position requires the individual to perform routine testing as scheduled to support production, and the stability program and completing required documentation. | 06/04/2021 |
| 8576 | Synthorx [Sanofi] East Swiftwater, PA Production Technician - Vaccine Bachelors degree. Exp: 0 + yrs |
Performs production in accordance with volume fluctuation, business need, and effective procedures. Responsible for Manufacturing activities in assigned area. Identifies all production issues and relays them to the leadership team. Works to prepare assigned areas for the oncoming shifts. Completes tasks and corresponding documentation as required by cGMP. | 06/04/2021 |
| 8577 | Synthorx [Sanofi] Framingham, MA Manufacturing Associate Bachelor’s degree. Exp: 1-3 years |
Position in a cGMP biologics facility which includes small scale and large scale upstream operations. Initial job responsibilities will include performing a diverse range of manufacturing related activities. The Manufacturing Associate will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 06/04/2021 |
| 8578 | Talaris Therapeutics Louisville, KY Quality Control Technologist I B.S. in Biology, Immunology or related field of science. Exp: less than 1 year |
The Quality Control Technician I/II is an entry-level position responsible for day-to-day support of the Quality Control (QC) laboratory and analytical testing related to the conduct of Phase I, II, and III clinical trials for a novel cell therapy. This includes calibration and maintenance of equipment, ordering and stocking of laboratory supplies, and performing analytical testing under Current Good Manufacturing Practices (CGMP) for production of a cell therapy product, immunologic monitoring of test samples, research and development. The primary responsibilities of this role focus on laboratory maintenance and manufacturing; secondary responsibilities may include clinical research and development and program organization activities. | 06/04/2021 |
| 8579 | Talis Biomedical Menlo Park, CA Sr/Research Associate, Assay Development BS or equivalent in Molecular Biology, Biochemistry, Biomedical Engineering, Biochemical Engineering, Chemical Engineering, or a related field. Exp: 1-5 years |
The successful candidate will assist in R&D reagent manufacturing and QC test development, perform biochemical and/or molecular testing to establish specifications and guard banding for reagents and processes. You will author, review, and edit SOPs, study protocols, reports and other documentation as needed. You will work collaboratively with others in Assay Development and also with other departments at Talis, including Assay Research, Operations, Quality, and Engineering. A strong understanding of nucleic acid biochemistry and experience working on cross-functional teams is highly desired. | 06/04/2021 |
| 8580 | Talis Biomedical Menlo Park, CA Manufacturing Engineer BS/MS degree in Mechanical Engineering or equivalent. Exp: 1-3 years |
This position will report to a Sr. Manufacturing Engineer and will be responsible for developing and documenting robust manufacturing processes for an IVD Consumable. This position is responsible for manufacturing processes performed at Contract Manufacturers as well as internal manufacturing processes. | 06/04/2021 |
| 8581 | Thrive Earlier Detection Baltimore, MD Lab Specialist I, Contract Associates Degree in Clinical Laboratory Sciences, Chemistry, Physics, Biology, or field as outlined in the essential duties. Exp: 1+ years |
The Laboratory Specialist will work closely with laboratory operations management to schedule and perform a variety of molecular biology procedures. This role will have a keen eye for process improvement and troubleshooting while following Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs). The Laboratory Specialist will also collaborate with other scientists and management to perform clinical laboratory testing meeting excellent quality standards. | 06/04/2021 |
| 8582 | Ultivue Cambridge, MA Lab Technologist Bachelor’s degree in a chemical, physical, biological, clinical laboratory science, medical technology, or related degree from an accredited instituti Exp: 1-3 years |
The laboratory technologist will conduct contract research offerings as part of Ultivue’s Assay Development and Services Laboratory. Laboratory work utilizes Ultivue’s InSituPlex™ technology for fluorescence multiplex IHC (mIHC). The lab technologist will support biomarker optimization and multiplex panel development activities to support services and U-VUE kits offerings. | 06/04/2021 |
| 8583 | Unity Biotechnology South San Francisco, CA RESEARCH ASSOCIATE 1 OR 2, IN VIVO PHARMACOLOGY Bachelor’s degree biology, physiology, bioengineering or related field. Exp: 1-4 years |
We are seeking to hire an exceptional Research Associate to join the in vivo pharmacology team. This position will be a critical part of a highly dynamic scientific research group supporting the characterization and development of drug candidates against novel drug targets. This role affords the individual the opportunity to work closely with a multi-disciplinary team, to deepen their expertise and knowledge in drug discovery, and to make key contributions to help bring new medicines to patients. | 06/04/2021 |
| 8584 | Unity Biotechnology South San Francisco, CA RESEARCH ASSOCIATE 1 OR 2 Master’s Degree in molecular or cellular biology, biochemistry, or related field. Exp: 0-2 years |
This lab-based position will be focused on developing and utilizing robust cell-based models to enable the exploration of novel biological pathways and the advancement of our Ocular programs. The successful candidate will be responsible for experimental design, execution and analysis, as well as presentations in project team and departmental meetings. In collaboration with other Discovery team members, this individual will play a key role in supporting the advancement of therapeutic candidates (small molecules, biologics or nucleic acids) through the generation of decision-driving data using rigorous and well controlled studies. | 06/04/2021 |
| 8585 | Unity Biotechnology South San Francisco, CA RESEARCH ASSOCIATE 1 OR 2, IN VIVO PHARMACOLOGY Bachelor’s degree biology, physiology, bioengineering or related field. Exp: 0-4 years |
Unity Biotechnology is seeking to hire a Research Associate to join the in vivo pharmacology team. This position will support preclinical efforts to characterize and develop drug candidates designed to improve human healthspan by modifying diseases associated with aging and cellular senescence. The candidate should be creative and have both a passion for biology and an interest in using animal models to study human disease. The position requires a self-motivated individual seeking a hands-on, lab-based role using in vivo animal models and in vitro methodologies to contribute to specific project goals as part of a dynamic team. The duties of the job include animal handling/dosing, experimental design and execution, analysis/interpretation of data, and presentation (verbal/written) of findings at team meetings. The successful candidate will also be expected to maintain compliance with animal care policies. | 06/04/2021 |
| 8586 | Universal Cells Seattle, WA Research Associate I BS Degree Exp: 0-3 years |
The primary purpose of the Research Associate I for Cell Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This entry-level Research Associate role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. This position will be provided training to perform all required fundamental skills to include record keeping, aseptic technique/cell culture, general lab operations, equipment use and maintenance, and some troubleshooting. Will assist with basic laboratory operations, and will keep appropriate documentation, including lab notebooks, batch documentation and experimental summaries. May assist in preparing controlled documents and data summaries. | 06/04/2021 |
| 8587 | ViaCyte San Diego, CA QC Associate (Job Code: 2021-25) bachelor’s degree, life sciences. Exp: 1 year |
This position will focus on quality control activities supporting the manufacture of therapeutic cell products, implantable devices, and cell therapy combination products. | 06/04/2021 |
| 8588 | ViaCyte San Diego, CA Associate Engineer I, Process Development (Job Code: 2021-15) BS/MS degree that included laboratory work in a Biology, Biomedical Engineering, or related field. Exp: 1+ years |
ViaCyte is seeking a highly motivated and talented individual to join the Process Development (PD) team in developing scalable production processes in bioreactors for a cell-based therapy to treat diabetes. The primary activities of the PD Associate/Engineer I will be to design and perform human embryonic stem cell (hESC) expansion and pancreatic cell differentiation experiments in small- and pilot-scale bioreactor systems to test feasibility and perform process optimization and characterization as well as develop closed processes for media exchange and cell harvest. Secondary activities include lab management, data entry, and support of other PD projects. This is a full-time position located in San Diego. | 06/04/2021 |
| 8589 | Viela Bio [Horizon] Gaithersburg, MD Associate Scientist, Analytical Sciences Research Associate: B.S. or M.S. degree in Cellular and Molecular Biology, Biochemistry, or related life sciences field. Exp: 0-1 year |
Horizon is looking for a highly motivated Research Associate or Associate Scientist to join the Analytical Sciences Department within Chemistry, Manufacturing, and Controls (CMC). The candidate will be responsible for supporting analytical characterization of clinical pipeline assets and help establish new lab operations and procedures. | 06/04/2021 |
| 8590 | Lonza Conley, GA Control Systems Engineer BS in Electrical Engineering, Computer Engineering or Computer Science Exp: 0+ Years |
LSI is seeking a Control Systems Engineer in the Metro Atlanta GA area to design, develop, install, commission & maintain state-of-the-art process control computer systems for the wood protection business, and provide remote system support to customer base in order to maintain optimum production. | 6/6/2021 |
| 8591 | Lonza Houston, TX Validation Engineer III BS in Relevant Scientific/Engineering Discipline Exp: 0+ Years |
The Validation Engineer will be responsible for the writing of and the execution of project and system qualifications, validation, re-qualifications, and revalidation of manufacturing facilities, equipment, utilities, computer system, and processes. | 6/6/2021 |
| 8592 | Lonza Houston, TX Quality Control Analyst, Environmental Monitoring BS in Microbiology, Biology, or Related Life Science Discipline Exp: 0+ Years |
The purpose of this role is to support the Quality Control, Environmental Monitoring (EM) team in maintaining the cleanrooms for commercial manufacture for both At Rest and In Operation conditions. This role will also be central in all processes associated with environmental monitoring and integral with environmental investigations, excursion report writing, and general upkeep of the micro department. | 6/6/2021 |
| 8593 | Lonza Portsmouth, NH Validation Specialist BS in Scientific or Technical Discipline Exp: 0+ Years |
QA Equipment Validation Specialist is responsible for supporting efforts that ensure all critical GMP equipment and systems are validated and maintained in compliance with user requirements, process parameters and global regulatory guidelines. The specialist works closely with Operations, Quality Assurance, Lonza clientele, and regulatory bodies with scientifically sound, documented evidence that our systems and processes will perform as required so they can be assured of a quality, compliant manufacturing environment. | 6/6/2021 |
| 8594 | Lonza Houston, TX Research Associate BS in Life Sciences, Chemical Engineering, or Biomedical Engineering Exp: 0+ Years |
The Research Associate provides technical support to lead scientists in conducting analytical tests for the evaluation of cellular products and in support of process development activities. | 6/6/2021 |
| 8595 | Lonza Hayward, CA EHS Specialist II BS in Relevant Scientific Discipline Exp: 0+ Years |
The EHS Specialist II will be responsible for maintaining the site Environmental, Health and Safety programs. The incumbent will have specific responsibility for both the implementation and maintenance of assigned programs in Environmental, Health and Safety programs. Will use EHS knowledge and experience to assist site personnel to achieve EHS objectives. | 6/6/2021 |
| 8596 | Lonza Walkersville, MD MSAT Scientist/Engineer MS in Chemical Engineering or Related Exp: 0+ Years |
The MSAT Engineer/Scientist will play a crucial role in Bioscience by leading Tech Transfers, complex technical investigations, and process improvements. This individual is the key process knowledge holder who drives the proactive life-cycle management through continuous and systematic optimization of production processes. The MSAT Engineer/Scientist is responsible for the incremental improvement of a process, but also ensures excellent process understanding and process robustness. As well as provides technical expertise in process risk assessment, technical complex investigations, CAPA management. Acts as a Subject Matter Expert in any of the following unit operations: Aseptic processing, cell culture, mixing, filtration/filling/finishing. | 6/6/2021 |
| 8597 | Loop Genomics San Jose, CA Service Research Associate BS/MS in Molecular Biology or Related Exp: 1-2+ Years |
The individual will provide next generation sequencing service to customers that incorporates Loop Genomics's long read technology with Illumina's short read sequencing platforms. This includes applying the standard operating procedure during NGS library preparation, as well as custom solutions tailored to the specific sequencing projects. The individual will also assist in testing and improving the robustness of Loop Genomics’s library preparation kits. This role requires excellent laboratory liquid handling skills and consistent performance of various wet lab operations. The individual will provide next generation sequencing service to customers that incorporates Loop Genomics's long read technology with Illumina's short read sequencing platforms. This includes applying the standard operating procedure during NGS library preparation, as well as custom solutions tailored to the specific sequencing projects. The individual will also assist in testing and improving the robustness of Loop Genomics’s library preparation kits. This role requires excellent laboratory liquid handling skills and consistent performance of various wet lab operations. | 6/6/2021 |
| 8598 | Loxo Oncology Boulder, CO Research Associate/Scientist, Biophysics BS/MS in Chemistry, Biology, Biochemistry, or Related Exp: 0+ Years |
The Biophysicist will characterize proteins utilizing cutting edge mass spectrometry, protein thermal melt methods, and other technologies. Additionally, the Biophysicist will evaluate protein-protein and protein small molecule interactions using a variety of enzymatic and biophysical techniques. Examples would include native mass spectrometry, SPR, fluorescence spectroscopy, TR-FRET and luminescence. | 6/6/2021 |
| 8599 | Loxo Oncology Boulder, CO Scientific Data Analyst, Scientific Systems BS in Chemistry or Related Exp: 0+ Years |
The Scientific Data Analyst will be responsible for the review and entry of data generated in a Discovery laboratory setting. The Scientific Data Analyst works with biologists, chemists, and scientific systems group to develop and maintain strategies to ensure integrity of published data. | 6/6/2021 |
| 8600 | Loxo Oncology San Francisco, CA Scientist/Senior Scientist, Proteomics BS/MS in Chemistry, Biology, Biochemistry, or Related Exp: 0+ Years |
This individual will serve as a technical lead and be responsible for carrying out experimental research aimed at understanding the role of proteins and post-translational modifications in oncology. An important focus is to study how proteins and protein interactomes are modulated by drug candidates. The researcher will have the opportunity to utilize and further develop state-of-the-art technologies for the discovery and characterization of receptor-ligand interactions. | 6/6/2021 |
| 8601 | Loxo Oncology San Francisco, CA Sr Research Associate/Associate Scientist, Mechanistic Biology/Proteomics BS/MS in Chemistry, Biology, Biochemistry, or Related Exp: 0+ Years |
The successful candidate will work as part of a collaborative team of scientists with expertise in protein production, cell culture, chemistry, biochemistry, structure, and biophysics, supporting hit-to-lead and lead-ID phases of Loxo oncology drug programs. The candidate will have opportunities to learn cutting edge techniques and to learn and develop technical expertise in protein biochemical and biophysical characterization. | 6/6/2021 |
| 8602 | LSI Solutions Victor, NY Design Quality Engineer I BS in Relevant Scientific/Engineering Discipline Exp: 0-3 Years |
Perform quality engineering tasks for new & existing product and process development and improvement initiatives. Quality Engineers are specialized in either Supplier Quality Engineering, Design Quality Engineering, Metrology Quality Engineering or Finished Goods Quality Engineering. Quality Engineers interface with other functions within an organization and with internal and external customers and suppliers on quality-related issues. | 6/6/2021 |
| 8603 | LSI Solutions Victor, NY Regulatory Associate BS in Relevant Scientific Discipline Exp: 0-2 Years |
Regulatory Associates assigned to Domestic Regulatory Projects will contribute to regulatory submissions, including FDA Q-Submissions, 513(g) Submissions, and 510(k) Submissions as required to market LSI’s new or modified medical devices in the U.S., including all relevant maintenance activities; and assist in providing regulatory feedback and guidance to the company throughout our medical device design and development process. Regulatory Associates assigned to Global Regulatory Projects will work with distributors to provide documents for regulatory submissions required to market LSI’s new or modified medical devices outside the U.S. | 6/6/2021 |
| 8604 | LSI Solutions Victor, NY Controls Engineer MS in Engineering, Engineering Technology or Related Exp: 1-3 Years |
The Controls Engineer is responsible for leading the design, debug, and installation of electro-pneumatic systems for production and new product development activities. The Controls Engineer is also responsible for researching, recommending, and implementing automated means to collect critical assembly and functional data to support production analytics. Supports development of specifications and validation of equipment. Support/Lead continuous improvement activities for existing manufacturing lines. | 6/6/2021 |
| 8605 | LSI Solutions Victor, NY Supplier Quality Engineer BS in Relevant Scientific/Engineering Discipline Exp: 0-3 Years |
This individual will perform quality engineering tasks for new & existing product and process development and improvement initiatives. Quality Engineers are specialized in either Supplier Quality Engineering, Design Quality Engineering, Metrology Quality Engineering or Finished Goods Quality Engineering. Quality Engineers interface with other functions within an organization and with internal and external customers and suppliers on quality-related issues. | 6/6/2021 |
| 8606 | Lubrizol Corporation Avon Lake, OH Quality Control Supervisor - TPU BS in Relevant Scientific/Engineering Discipline Exp: 0+ Years |
Responsibilities: Supervises day-to-day activities in the QC laboratory. Maintains all lab ISO documentation, including procedures and calibration records. Verifies that instruments are maintained per ISO requirements. Supports new manufacturing authorizations from QC testing perspective for products. Supports the LifeScience Polymer business by confirming all requirements are in place for medical polymers. | 6/6/2021 |
| 8607 | Lubrizol Corporation Franklin, WI Quality Engineer BS in Relevant Scientific/Engineering Discipline Exp: 0+ Years |
The Quality Engineer is primarily responsible for assuring product and Quality Systems quality and compliance through the development, implementation and monitoring of appropriate processes, tools, metrics and goals. The Quality Engineer is the process owner for the site CAPA program, process validations, Customer Complaints, NCRs, CAPAs, Internal Audits, and assigned New Product Development programs. | 6/6/2021 |
| 8608 | Lubrizol Corporation Brecksville, OH Process Development Engineer BS/MS in Chemical Engineering Exp: 1+ Years |
Responsibilities: Supervises, leads, and supports Life Science Health aromatic and aliphatic TPU product development, product scale-up, process capability improvement, and new raw material evaluation projects. Collaborates with multifunctional project teams of scientists, engineers, account managers, and product management for new product development projects for successful scale-up and product realization. Designs, executes, analyzes, and reports (both written and verbal) on multiple, simultaneous complex projects within pilot plant and commercial scale manufacturing. Coordinates and consults on new capital projects as needed. Designs experiments and analyzes data from both the laboratory and pilot plant. | 6/6/2021 |
| 8609 | Lubrizol Corporation Brecksville, OH Footwear Applications Engineer BS/MS in Chemical, Mechanical, Polymer, or Textile Engineering. Exp: 0+ Years |
As a Footwear Applications Engineer you will lead new product development programs targeted in the footwear industry, related to molded parts or films. A key function of this role is to develop test protocols for finished parts related to end use performance, while also serving as a key technical contact for major footwear partners. | 6/6/2021 |
| 8610 | Lubrizol Corporation Wilmington, MA Manufacturing Engineer BS in Chemical or Mechanical Engineering, Chemistry, or Related Exp: 0+ Years |
Under the direction of the Manufacturing Manager, the Manufacturing Engineer serves as a technical resource for Operations personnel, applying technical skills within production, optimizing plant operations, resolving plant problems and enabling the safe and efficient production of quality products. This role assists teams with daily operations and process performance to run a low cost, on specification, reliable, and optimized operation, maximizing value to the business in a safe, environmentally friendly manner. | 6/6/2021 |
| 8611 | Lumen Bioscience Seattle, WA Lab Aide BS in Biology or Chemistry Exp: 0+ Years |
The Lab Aide’s responsibilities include working closely with Lumen's Lab Operations Team Lead to perform various cleaning, solution/media prep, and organizational tasks. To succeed in this role, you should have excellent time management and communication skills. Ultimately, the Lab Aide’s goal will be to facilitate the effective management of the Lab Operations team, according to the organization’s standards. | 6/6/2021 |
| 8612 | Luminex Northbrook, IL Associate Scientist II MS in in Biological/Chemical Science or Related Exp: 0+ Years |
The individual will participate in the company's day to day research activities which include: design, execution and interpretation of scientific experiments and design and development of assays based on Luminex's technology platform and chemistries. The position will carry out scientific experiments independently with minimal supervision. | 6/6/2021 |
| 8613 | Luminex Austin, TX Technical Applications Specialist BS in Biology, Molecular Biology, or Related Exp: 0-2 Years |
Responsibilities: Receiving complaints and inquiries from customers and partners for all Luminex supported products. Documenting all customer communications, triage complaints as required, and lead investigations for issue resolution. Contributing to the maintenance of the Install Base, Knowledge Management database, and all administrative duties associated with Technical Support. Performing laboratory duties when needed as part of troubleshooting efforts, coordinating with other departments (Business Managers, Field Service and Molecular/Field Applications Support teams, QA, RA and Operations) for customer management and issue resolution. Perform independent data analysis and problem solving. | 6/6/2021 |
| 8614 | Luminex Madison, WI Associate Scientist I - Design Transfer and On Market Support BS in in Biological/Chemical Science or Related Exp: 1+ Years |
The Associate Scientist I – R&D DT & OMS (Design Transfer & On Market Support) is vital for all stages of the product development process and will participate in transfer of new product designs to manufacturing beginning in the early stage of new product development through implementation and also include On-Market support activities post-product launch. This role's primary responsibilities will include coordination of the transfer of new product designs from R&D to manufacturing operations, including Bill of Materials (BOM), product design and configuration, product specifications, and QC test methods. | 6/6/2021 |
| 8615 | Luminex Austin, TX Associate Scientist II - Applications & Development MS in in Biological/Chemical Science or Related Exp: 0+ Years |
The individual will participate in the company's day to day research activities which include: design, execution and interpretation of scientific experiments and design and development of assays based on Luminex's technology platform and chemistries. The position will carry out scientific experiments independently with minimal supervision. | 6/6/2021 |
| 8616 | Luminex Northbrook, IL Quality Control Associate I, Reagents BS in Chemistry, Biochemistry, Biology, or Related Exp: 1+ Years |
Responsibilities: Executing core Quality Control (QC) processes associated with reagent consumable and bioassay production, reagent stability program, and controlled storage monitoring. Assisting with incoming quality control, departmental calibration and maintenance and the retention program. Maintaining QC laboratory supplies, preparing internal use laboratory reagents, as well as maintaining the integrity and cleanliness of QC work and storage areas. Participating in QC processes associated with test method development, product development, and equipment/ method validations. | 6/6/2021 |
| 8617 | Luminex Austin, TX Technical Writer & Field Service Specialist BS in Technical Scientific Writing or Related Exp: 0-2+ Years |
Responsibilities: Joining an energetic Technical Communications team, with skills in technical writing, hardware and software engineering, multimedia development, and instructional design. Developing and updating internal and end-user content including manuals, package inserts, quick guides, multimedia, etc. for use and support of Luminex products with a focus on Field Service. Collaborating with Technical Product Management and other Luminex teams to write technical product content that simplifies complex concepts, presents information attractively, and maximizes user comprehension and information retention. | 6/6/2021 |
| 8618 | LSNE Contract Manufacturing Madison, WI QA Specialist I - Audits MS in Relevant Scientific Discipline Exp: 1-5 Years |
This position is responsible for maintaining and adhering to LSNE and regulatory compliance requirements for established quality system programs by performing internal audits, hosting client audits and providing assistance during regulatory agency inspections. Additionally, this position plays a key role in maintaining the Material and Supplier Qualification programs for all LSNE facilities. | 6/6/2021 |
| 8619 | LSNE Contract Manufacturing Manchester/Bedford, NH Scientist I - Process Development BS/MS in Biology, Biochemistry, Chemistry, Biotechnology, Chemical Engineering, or Related Exp: 0-3 Years |
Responsibilities: Executes experiments under direct supervision supporting Process Development projects. Accurately follows and completes required documentation (batch records, forms). Expected to adhere to all procedures, including gowning and safety requirements, at all times. Assists in troubleshooting development equipment, as assigned. Completes all required training in a timely manner Collaborates with Process Development Scientists and Management during technical transfer and experiment design. | 6/6/2021 |
| 8620 | Jordi Labs Mansfield, MA Chemist Master’s degree in chemistry or other closely related field. Exp: one year |
1) Prepare technical reports 2) Interpret gas chromatograph mass spectrometry (GCMS) and liquid chromatograph mass spectrometry (LCMS) results with a high level of proficiency 3) Interpret chromatographic data including high performance liquid chromatography (HPLC), gas chromatography (GC), and gel permeation chromatography (GPC) results 4) Combine results from multiple techniques to identify unknown chemical compounds 5) Quantify chemical components using HPLC and GC results 6) Work with a team of scientists to design and implement analytical strategies 7) Perform or oversee complex analytical strategies with an emphasis of MS and chromatography 8) Review technical reports written by other scientists | 5/24/2021 |
| 8621 | Karius Redwood City, CA Research Associate B.S. in Biology, Molecular Biology, Genetics or related field. Master’s degree preferred. Exp: 1-3 years |
As a Research Associate you will work alongside scientific leaders in NGS-based infectious disease diagnostics providing meaningful contributions to making an impact in the lives of patients while contributing to the company’s growth and development . You will be responsible for maintaining process excellence for a state-of-the art NGS infectious disease diagnostic assay by assisting in an established in-house manufacturing process. You will be also involved with several exciting research projects and be at the forefront of non-invasive diagnostics working alongside our scientists to deliver new products. The ideal candidate should have experience with nucleic acids, NGS, or other molecular biology assays to conduct laboratory experiments on research projects under the direction of senior lab personnel. | 5/24/2021 |
| 8622 | Kem Pharm Coralville, IA Laboratory Assistant Candidates must currently possess, or currently be pursuing, a four-year degree in Life Sciences and Biotechnology field, including Chemistry, Biology Exp: recent graduate |
The Laboratory Assistant requires a recent graduate, or student currently pursuing a biotech-related degree, who will utilize basic biological, chemical, physical, and life science laboratory skills to perform the following responsibilities: • Reports directly to the Senior Group Leader, Chemistry, and indirectly to the EVP, Research & Development, and supports the entire R&D team • Follows standard operating procedures (SOP) for maintaining laboratory equipment and facilities • Assists in the preparation and/or prepares solutions, reagents, starting materials • Performs routine laboratory tests, chemical reactions, and isolation/purification procedures • Coordinates and/or conducts laboratory equipment maintenance and calibration • Keeps laboratory supplies up-to- date and using Quality Assurance techniques and assists with inventory, ordering, receiving and stocking of laboratory supplies and equipment • Keeps clear, accurate and timely records of all laboratory work and data measurements • Maintains and organizes Safety Data Sheets (SDS’s) and Certificates of Analysis (COA’s), as well as any other documentation required for technical information about the products • Performs general lab housekeeping and instrument clean-up • Efficiently organizes, prioritizes, and plans work schedules • Regularly and effectively communicates with other R&D personnel and supervisor regarding all aspects of the day to day operations of the laboratory • Performs various other research-related duties as assigned | 5/24/2021 |
| 8623 | Kriya Therapeutics Morrisville, NC Research Associate I/II BS degree is Biochemistry, Chemistry, Molecular Biology or other science field with relevant course completion. Exp: RAI 0-1 years |
We are seeking a energetic candidate that will execute a range analytical techniques in support of AAV gene therapy method, process and formulation development. The position is heavily focused on benchwork and the applicant should have a desire to continue in a laboratory focused role. If you want to be a part of a fast paced start up company, please join us. | 05/25/2021 |
| 8624 | Krystal Biotech Pittsburgh, PA Research Associate, Analytical Development Bachelor’s degree (Biology, Biochemistry, Chemistry, or related science). Exp: 0-2+ years |
Krystal Biotech, Inc is seeking a highly motivated Research Associate to perform high quality analytical development to support research for gene therapy products. This position will be laboratory based. | 05/25/2021 |
| 8625 | KSQ Therapeutics Cambridge, MA Associate Scientist/Scientist, Immunobiology B.S. or M.S. in biology, immunology, or relevant field. Exp: 1+ year(s) |
KSQ Therapeutics, Inc. is seeking a self-motivated and dependable Associate Scientist/Scientist to join our Immunobiology team. Our ideal candidate thrives in a research environment that demands scientific rigor and technical excellence. Applicants with an interest in myeloid cell/T cell immunology and expertise in cell culture, CRISPR-Cas9 technology and molecular cloning are strongly encouraged to apply. | 05/25/2021 |
| 8626 | KSQ Therapeutics Cambridge, MA Associate Scientist/Senior Associate Scientist, Oncology Associate Scientist: BS degree. Exp: 1-2 years |
KSQ Therapeutics, Inc. is seeking an exceptional and highly motivated scientist to apply their experience in oncology towards the discovery of the next generation of impactful therapies. This person will contribute to cell biology and translational efforts for our drug discovery pipeline. This skilled scientist will characterize novel cancer pathways and develop assays for drug targets. They must be driven and flexible with the broad number of in vitro, in vivo, and biomarker activities associated with cancer drug discovery. This is an opportunity to learn, contribute and flourish in KSQ’s dynamic, highly interdisciplinary, and collaborative environment. | 05/25/2021 |
| 8627 | KSQ Therapeutics Cambridge, MA Associate Scientist/Scientist, Target Discovery Associate Scientist: BS degree. Exp: 1-3 years |
KSQ Therapeutics, Inc. is seeking an exceptional and highly motivated scientist to apply their experience in molecular biology towards the discovery of the next generation of impactful therapies. This skilled scientist will contribute to target validation and cell biology efforts to characterize novel cancer pathways and develop assays for drug targets. They must be driven and flexible with the broad number of in vitro, in vivo, and biomarker activities associated with cancer drug discovery. This is an opportunity to learn, contribute and flourish in KSQ’s dynamic, highly interdisciplinary, and collaborative environment. | 05/26/2021 |
| 8628 | Kura Oncology San Diego, CA Research Associate BA or BS degree in biology. Exp: 6 months |
We’re looking for a Research Associate to join our growing team. This is a newly created position due to company growth. The Research Associate will support scientists with day-to-day management of laboratory and experiments involving cell biology, molecular biology, and biochemistry techniques. Training and mentoring will be provided for the skills and knowledge involved. This is an excellent opportunity for those who are motivated, eager to learn, and adapt quickly to changing needs in the lab. | 05/26/2021 |
| 8629 | LakePharma Hayward, CA Associate Scientist II, Mammalian Cell Culture and Purification [JC-1349B] M.S. in biochemistry, chemical engineering or related field (salary will depend on education and experience). Exp: 1+ year |
We are rapidly growing and seeking a talented individual to join our Process Development team as a full-time Scientist I/Postdoc. | 05/26/2021 |
| 8630 | LakePharma Hopkinton, MA QC Microbiology Analyst I, Analytical Development and Quality Control [JC-1430] BS required or MS preferred in life sciences including biology, immunology, biochemistry, process engineering or a similar biological science. Exp: 0-3 years |
The ideal candidate will support cGMP method validation, equipment validation, qualification and release testing for raw materials, drug substance and finished product testing for products produced at Lake Pharma’s GMP manufacturing facility and affiliated contract organizations. The individual will have a focus on Microbiology and Chemistry, including Bioburden, Endotoxin, Sterility, TOC, Environmental monitoring, PW/WFI water collection regulations, clean room experience and Micro id. He/she will develop methods, qualify and validate equipment and support investigations for OOS and other non-conforming results. He/she will contribute to the implementation of testing capabilities, related validation and qualification activities, investigations and assay/instrument troubleshooting with a high degree of independence. | 05/26/2021 |
| 8631 | LifeMine Therapeutics Cambridge, MA Research Associate II, Synthetic Biology M.S. in molecular biology, microbiology, biochemistry, or a related field. Exp: 0-2 years |
We are seeking a Research Associate for our Cambridge site to join our Synthetic Biology team. The Research Associate will be involved in developing and operating our platform for the high throughput engineering of filamentous fungi for the identification and production of natural products to further LifeMine’s fungal genomically enabled drug discovery platform. | 05/27/2021 |
| 8632 | Life Sensors Malvern, PA Entry Level Scientist BS or MS in biological sciences or related degree. Exp: 0-2 years |
We are seeking individuals who are passionate about research, bring out of the box thinking and take bold steps to develop innovative technologies with applications in the ubiquitin research field. Successful candidates will have basic knowledge of biochemistry and molecular biology techniques, in particular experience with protein expression and purification and cloning. Knowledge of the ubiquitin proteasome pathway is desired. | 05/27/2021 |
| 8633 | Ligand Pharmaceuticals Durham, NC Associate Scientist, Cell culture/molbio (Entry Level) BA/BS in biology or cellular/molecular biology. Exp: 0-2 years |
Icagen’s facility in Durham, North Carolina currently has an opening for a talented scientist to join our biology team. This is a full-time, laboratory-based position offering an opportunity to play key roles in identifying novel drug candidates and advancing drug development projects. The ideal candidate will have experience in a broad set of cellular and molecular biology techniques with a fundamental understanding of molecular biology. The successful candidate will be capable of managing multiple projects simultaneously while working as part of a core team. The work will be fast-paced and process-oriented in a dynamic environment which is predicated upon continuous improvement where everyone is encouraged to contribute to improving laboratory efficiency. | 05/28/2021 |
| 8634 | Ligand Pharmaceuticals Emeryville, CA Research Assistant/Associate B.Sc. Exp: 0-2 years |
(position level depends on experience; we are looking to fill 2 positions within this department) The Senior Research Associate works under the direction of a senior level scientist supporting Ligand’s OmniAb Technology Platform with responsibilities in multiple research areas including: generating and characterizing new strains of OmniChickens; conducting OmniAb antibody discovery campaigns for internal and partner programs; preparing custom protein reagents for immunization and screening; antibody engineering and optimization of lead molecules for further development. | 05/28/2021 |
| 8635 | Likarda Kansas City, MO R&D Scientist (Cell Culture and Biology) Bachelors or Masters degree in biological sciences or engineering. Exp: 1 year |
Likarda is at the forefront of improving and providing cell-based therapies and is seeking a scientist to further develop these efforts. The successful candidate will be a member of the cell culture team, working on internal projects as well as external client projects. The candidate will support the program with aseptic cell culture and cell maintenance, completing assays, writing reports, and providing general laboratory support. This will require the candidate to draw on their expertise from a range of experiences in biology, cell culture methods, aseptic technique, and other general lab principles. | 05/28/2021 |
| 8636 | LYGOS Berkeley, CA Analytical Chemistry Research Associate B.S. degree in chemistry or related field. Exp: 0 - 3 years |
Lygos is seeking an analytical chemistry research associate candidate to set up, run, clean, and maintain HPLC instruments. The successful candidate will have experience with general lab procedures, data interpretation, and reporting in a fast-paced and dynamic work environment. | 05/28/2021 |
| 8637 | Mammoth Biosciences Brisbane, CA Laboratory Technician, Diagnostic Operations Associate's degree in Biotechnology. Exp: 0-2 years |
Mammoth is seeking a Diagnostic Operations Laboratory Technician to support our research and product development teams. This individual will assist by manufacturing and providing quality control of standard reagents for ongoing projects, maintaining laboratory equipment and performing routine monitoring of the laboratory. The ideal candidate will have experience with molecular assays (qPCR, ddPCR) and in assembling a variety of molecular mastermixes and buffers. The candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. | 05/28/2021 |
| 8638 | Minnetronix Medical St Paul, MN Electrical Engineer I Bachelor’s degree or equivalent in Electrical Engineering, Computer Engineering, or Physics required. Exp: 0-3 years |
As a n Electrical Engineer I at Minnetronix, you’ll work on analog and digital circuit design , embedded system and microcontroller-based design, sensor interfaces, A/D conversion, filtering, and PCB schematic design to support new product designs. Working under close engineering supervision on a cross-functional team, you’ll help bring medical devices from concept through development and into productions. We have a broad client base so project assignments will span an array of products, be broad in nature, and require creativity and ingenuity. | 05/28/2021 |
| 8639 | Minnetronix Medical St Paul, MN Process Development Engineer I Bachelor’s degree in an engineering, technical or scientific discipline. Exp: 0 to 2 years |
This Process Development Engineer I will work cross functionally and lead the transfer of medical devices and respective processes into commercial manufacturing. A Process Development I is responsible for Introduction of new products and processes. Their responsibilities include: new product introduction, Identification and development of new manufacturing processes, pilot manufacturing, production cell layout, supplier development and selection, Manufacturing documentation, issue tracking and resolution, and continuous improvement. | 05/28/2021 |
| 8640 | Minnetronix Medical St Paul, MN Software Engineer I BS or equivalent in Computer Science, Software Engineering or similar field. Exp: 0-3 years |
As a Software Engineer I at Minnetronix, you’ll design, implement and test real-time embedded medical device software and supporting applications and prototypes. Working under close engineering supervision on a cross-functional team, you’ll help bring medical devices from concept through development and into production . We have a broad client base so project assignments will span an array of products, be broad in nature, and require creativity and ingenuity. | 05/28/2021 |
| 8641 | Mission Bio South San Francisco, CA Research Associate R&D A B.S. / B.A. in Molecular Biology / Cell Biology / Biochemistry or associated fields. Exp: 1-2 years |
We are looking for a highly self-motivated individual to join the R&D Team as Research Associate. This exciting and challenging role is responsible for performing studies related to current and future product development. The position will be critical in generating analytical and experimental data related to Mission Bio’s products. | 05/28/2021 |
| 8642 | MOBILion Systems Philadelphia, PA Lab Support Coordinator Bachelors in analytical chemistry, chemistry, biology, or engineering. Exp: 1-3 years |
The Lab Support Coordinator will be responsible for major contributions to the efficient and safe operation of the MOBILion labs. In the immediate term, the candidate will be responsible for creating and maintaining lab operations processes including inventory, documentation, and safety document generation and compliance. The candidate will also provide general lab support as needed for the different departments in the company. This position offers the candidate the opportunity to help bring new technology into the Life Science application space by ensuring the entire team can operate safely and efficiently in the lab space. The position requires a highly motivated and organized person with a reputation for integrity and accountability with sound organizational and interpersonal skills. The ideal candidate will be a self-starter and independent contributor with a strong operational focus. | 05/28/2021 |
| 8643 | NAMSA Northwood, OH Chemist Master’s degree in chemistry. Exp: 0+ years |
Independently conduct testing according to written instructions. May be requested to conduct more involved studies. May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. May conduct routine testing per NAMSA SOPs as well feasibility, protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP, etc. Works with management to ensure large studies are completed on or before the due date. Prepare and maintain the reagents required for testing. May mentors and train staff in general laboratory testing as well as offering more complex instrumentation training. Maintain ancillary records. Analyze data, perform calculations, and interprets results May trend and evaluate QC data as appropriate. May assist with SOP, purchase specification, protocol, and work instruction creation and revisions. Participate in the improvement of documents, test systems, quality systems, and workflow. Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and taking all concerns to management as required. Review work of other colleagues for scientific soundness and GLP/GMP and SOP compliance. Helps ensure department compliance to site goals and objectives (i.e. financial, OPD, report revision). May be responsible for final report signing. In the event of test failure, leads failure investigations identifying root cause and corrective/preventive actions. May be responsible for client contact with regards to unexpected testing results, project updates, and deliverables. Assist with Client Audits as needed. Other duties as assigned. | 05/28/2021 |
| 8644 | NAMSA Remote - Northwood - USA, US Chemist Master’s degree in chemistry. Exp: 0+ years |
Independently conduct testing according to written instructions. May be requested to conduct more involved studies. May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. May conduct routine testing per NAMSA SOPs as well feasibility, protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP, etc. Works with management to ensure large studies are completed on or before the due date. Prepare and maintain the reagents required for testing. May mentors and train staff in general laboratory testing as well as offering more complex instrumentation training. Maintain ancillary records. Analyze data, perform calculations, and interprets results May trend and evaluate QC data as appropriate. May assist with SOP, purchase specification, protocol, and work instruction creation and revisions. Participate in the improvement of documents, test systems, quality systems, and workflow. Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and taking all concerns to management as required. Review work of other colleagues for scientific soundness and GLP/GMP and SOP compliance. Helps ensure department compliance to site goals and objectives (i.e. financial, OPD, report revision). May be responsible for final report signing. In the event of test failure, leads failure investigations identifying root cause and corrective/preventive actions. May be responsible for client contact with regards to unexpected testing results, project updates, and deliverables. Assist with Client Audits as needed. Other duties as assigned. | 05/28/2021 |
| 8645 | Nanomix Emeryville, CA Research Associate Bachelor of Science (or foreign equivalent) in in Chemistry, Chemical Engineering, Biology, Bioengineering or related field. Exp: 3+ months |
Design and develop new cartridge prototypes, working with biosensors, filters, conjugate pads, microfluidics, device programming, etc. to enable specific biological assays on the eLab platform. Design processes required to manufacture product components by developing fixtures (CAD, Laser Printer, 3D Printer, Solidworks etc.), installing necessary components on machinery (Vacuum, Pressure Gauge, Pressure Regulator etc.), scripting robotic liquid handlers, drafting qualification requirements, and writing quality documentations. Design and execute biological wet lab experiments using ELISA, enzymatic assays, chromogenic assays, fluorescence/chemiluminescence. Work with electrochemical (CV, chronocoulommetry) and analytical (FTIR, Raman) tools to characterize biosensors and their performance. Develop quality control methods and implement them in the quality system. Perform large scale data analysis using JMP, PRISM, MATLAB, and Python to analyze research data and manufacturing data. | 05/28/2021 |
| 8646 | nanoComposix San Diego, CA Manufacturing Laboratory Technician Bachelors Degree. Exp: 0-1 years |
A laboratory technician position is available at nanoComposix. Responsibilities include working with the team to ensure that the lateral flow production schedule is maintained, all quality control measures are in place and followed, all reagents and cards are manufactured, processed and characterized as specified under a formal quality system, all team members are trained and have all of the tools necessary for success. | 05/28/2021 |
| 8647 | Notable Labs Foster City, CA Associate Scientist Bachelor’s Degree in cell biology, molecular biology, or related field. Exp: 1-2+ years |
Notable Labs is looking for a curious, inspired, entrepreneurial scientists to join our research and development team. We work in an incredibly fast-paced environment that thrives on creativity, learning, and innovation. Given our small size, you’ll be able to make valuable contributions to the goals and strategic direction of both the science team and the company broadly. Just as you are investing in us, we want to invest in you. Working alongside our existing team, you’ll have generous opportunities for personal and professional growth. As a member of a transformative translational medicine platform, you’ll personally have a direct impact on patient outcomes and the future of cancer care. | 05/28/2021 |
| 8648 | Noveome Biotherapeutics Pittsburgh, PA QC Analyst II MASTER’S DEGREE IN A BIOLOGICAL SCIENCE. Exp: 1+ YEARS’ |
The Quality Control Analyst II is responsible for conducting routine chemical and biological testing of raw materials, intermediates, finished products, and stability samples. This position works independently while following defined standard operating procedures. This position also documents the testing process, performs an initial review of testing results and identifies trends. The Quality Control Analyst II will maintain data integrity and ensure compliance with laboratory safety procedures. | 05/28/2021 |
| 8649 | Oakwood Labs Oakwood Villiage , OH Biochemist / Chemist - Entry Level Bachelor’s degree in chemistry, biology, or related discipline. Exp: Entry Level |
This is an excellent entry-level opportunity for those interested in working at a technology-based pharmaceutical company. There will be training rotations in the research and development lab and the quality control lab. | 05/28/2021 |
| 8650 | Exagen Diagnostics Vista, CA Clinical Laboratory Scientist (Automated Chemistry), Vista Bachelor's degree from four-year College or University. Exp: one to three years |
A current and valid California State Clinical Laboratory Scientist License (CLS) or Clinical Chemistry Scientist (CCS). The Clinical Laboratory Scientist is responsible for high complexity testing and analysis to obtain data for use in diagnosis and recording laboratory test results. | 5/13/2021 |
| 8651 | EXONBIO San Diego, CA Research Associate Master Degree in Biology. Exp: One year |
We are looking for a RESEARCH ASSOCIATE to join our antibody development team. | 5/13/2021 |
| 8652 | Foghorn Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Biochemistry & Biophysics BA/BS or MS degree in Biochemistry, Biophysics, Enzymology. Exp: 0-3 years |
We seek a highly motivated, enthusiastic and collaborative researcher to join our Drug Discovery team in a lab-based role to support early discovery projects in oncology. | 5/14/2021 |
| 8653 | GenMark Diagnostics Carlsbad, CA Research Associate I B.S. degree in Chemistry, Biochemistry, Molecular biology or related field. Exp: one (1) year |
You will execute a range of molecular biology procedures, reagent preparation, and bioanalytical procedures and laboratory duties under supervision. Performing lab duties while maintaining associated health and safety guidelines while maintaining inventory of laboratory reagents and supplies. | 05/14/2021 |
| 8654 | GenMark Diagnostics Carlsbad, CA Mechanical Engineer I Minimum of BS degree in Mechanical Engineering Exp: 0-2 years |
Under supervision from senior contributors, serve as a mechanical engineer for concept-to-market and sustaining engineering efforts of IVD instrumentation. Apply hands-on involvement in on-market support for existing and new products, troubleshooting and root cause analysis, creation and maintenance of input and output specifications, concept and feasibility activities, prototyping, testing, and transfer to manufacturing. | 05/14/2021 |
| 8655 | GenMark Diagnostics Carlsbad, CA Electrical Engineer I Minimum of BS degree in Electrical Engineering. Exp: 1-2 years |
This new exciting role at GenMark will work under supervision from senior contributors, serve as an electrical engineer in sustaining engineering and concept-to-market efforts for IVD instrumentation. Apply hands-on involvement in on-market support for existing and new products, troubleshooting and root cause analysis, creation and maintenance of input and output specifications, concept and feasibility activities, prototyping, testing, and transfer to manufacturing. | 05/14/2021 |
| 8656 | GRAIL Menlo Park, CA Quality Control Research Associate I (Contract) B.S. in a relevant field required. Exp: 1+ years |
GRAIL is seeking a Research Associate for the Lab Operations Manufacturing Sciences and Technology team (MSAT), who will be primarily responsible for materials quality control (QC) and associated tasks. | 05/17/2021 |
| 8657 | GRAIL Menlo Park, CA Laboratory Technician 1/2 B.S required in a relevant scientific field. Exp: 1 - 5 years |
GRAIL is seeking a Laboratory Technician 1/2 for the R&D Laboratory Management team, who will be primarily responsible for ensuring the efficient operation of GRAIL Research and Development activities. The ideal candidate is a detail-oriented, dynamic team player with experience in both automated and manual molecular biology workflows combined with strong interest in NGS methodologies. | 05/17/2021 |
| 8658 | GRAIL Menlo Park, CA Clinical Laboratory Associate, Accessioning - Long Term Contract (Tues-Sat 7:00am-3:30pm OR 8:30am-5:00pm) Bachelor of Arts or Science in Molecular Biology or related field. Exp: A minimum of 1 year |
The Clinical Laboratory Associate (CLA) - Accessioning will assist in building and establishing GRAIL’s Clinical Laboratory, performing specimen testing and supporting the daily operations of the Clinical Laboratory. The focus of the CLA - Accessioning will be on the receipt, triage, accession, and centrifugation of patient samples submitted to the CLIA laboratory for testing. | 05/17/2021 |
| 8659 | GRAIL Menlo Park, CA Clinical Laboratory Associate, Accessioning - Long Term Contract (Mon-Fri Noon-8:30pm OR 1:00pm-9:30pm) Bachelor of Arts or Science in Molecular Biology or related field. Exp: A minimum of 1 year |
The Clinical Laboratory Associate (CLA) - Accessioning on the swing shift will assist in building and establishing GRAIL’s Clinical Laboratory, performing specimen testing and supporting the daily operations of the Clinical Laboratory. The focus of the CLA - Accessioning will be on the receipt, triage, accession, and centrifugation of patient samples submitted to the CLIA laboratory for testing. | 5/17/2021 |
| 8660 | GRAIL Raleigh-Durham, NC Clinical Laboratory Associate 1 (New Grad - Fall 2021) Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or a related field preferred. Exp: New Grad (Fall 2021) |
The Clinical Laboratory Associate 1 is responsible for assisting the Clinical Laboratory Scientist and supporting the daily operations of the Clinical Laboratory. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask, be flexible with tasks and schedules and ability to work independently in a team environment. | 05/17/2021 |
| 8661 | Gritstone Oncology Pleasanton, CA QUALITY CONTROL ANALYST 1/2 (CONTRACTOR) Bachelor’s degree (or equivalent) in scientific discipline. Exp: 0 to 5+ years |
The primary role of the QC Analyst is to conduct cGMP analytical testing for raw materials, in process, finished product, stability and other samples to support development and manufacturing operations. This role will work closely with senior analyst(s) and the Development group to implement analytical methods in Quality Control. | 05/18/2021 |
| 8662 | Guardant Health Redwood City, CA Research Associate I, Technology Development Sustain & Support B.S. Exp: 1-3 years |
As a Research Associate I in Technology Development, Sustain & Support, you will work within the team to support current sustaining efforts as well as interface with outside teams including process engineering, clinical operations, research operations, product management, and bioinformatics. You will be hands on in the lab and be required to use existing assays and/or assay prototypes to generate data in support of validating existing workflows or creating new technologies related to liquid biopsy sequencing. | 05/18/2021 |
| 8663 | Histo Tox Labs Boulder, CO Research Associate I (Scanning) Bachelor's degree in Biochemistry, Biology, or a related field. Exp: entry-level position |
We are seeking a Research Associate I to assist the Image Analysis (Brightfield) Department with scanner and scanning related tasks. Note: This is an entry-level position. | 05/18/2021 |
| 8664 | ImmuneID Cambridge, MA Research Associate / Senior Research Associate – Platform Master’s s degree in biology, biochemistry or a relevant scientific discipline. Exp: 1+ years’ |
We are seeking a talented and collaborative molecular biologist to perform and develop large scale screening studies, technology optimization and confirmatory assays. The successful candidate will work closely with team members and support discovery and pre-development programs. | 05/18/2021 |
| 8665 | InBios International Seattle, WA Production Associate - Biotechnology BS Exp: 0-2 years |
The Production Associate is responsible for assembly and/or packaging activities which include but are not limited to any of the following processes: operation of all Auto-assembly machinery, Filling equipment and Web lamination machinery used in the production areas. | 05/19/2021 |
| 8666 | IntelliSyn R&D Montreal, QC, CA Synthetic & Medicinal Chemistry Scientists: Multiple Positions; BSc, MSc, PhD BSc, MSc Exp: 0-2 years' |
IntelliSyn Pharma is looking for motivated Associate Scientists to help drive our drug discovery programs. | 05/19/2021 |
| 8667 | Pace Analytical Naperville, IL Lab Tech - Micro & Molecular Bachelor's degree in Biology required Molecular Biology or Microbiology preferred Exp: 1+ year |
Our client has an opening for a Lab Technician on their Legionella Lab team, located in Naperville, Illinois. This is an entry-level position to support the RD&E community. | 05/19/2021 |
| 8668 | Pace Analytical Eden Prairie, MN Chemist - Entry-Level HPLC Bachelor's degree in Chemistry or related science. Exp: 0-2 years |
This position will actively support product development of coatings for medical devices though analytical testing. The products being developed are crucial to patient’s safety and health within the healthcare industry. Work is performed as part of a team in a collaborative environment. | 05/19/2021 |
| 8669 | Pace Analytical Boothwyn, PA Scientist I Bachelor’s degree in chemistry or related science field. Exp: 1-3 years |
This position will actively support the quality control testing of pharmaceutical raw materials and finished products through analytical testing. The products being monitored are crucial to patient’s safety efforts within the healthcare industry. Work is performed as part of a team in a collaborative environment. | 05/19/2021 |
| 8670 | Invicro Boston, MA Associate Scientist, Imaging BS in bioengineering, biomedical engineering, medical physics, radiologic sciences, pharmacology or other engineering degree. Exp: 0-3 years |
Invicro is currently looking for an Associate Scientist who will assist with in vivo, small animal medical imaging studies, including nuclear medicine studies (PET/SPECT), computed tomography (CT), and magnetic resonance imaging (MRI) in the context of a multi-modal imaging laboratory to aid in the development of novel therapeutics. | 05/19/2021 |
| 8671 | InVivo Scribe San Diego, CA Development Associate I BS Degree in a technical or scientific discipline. Exp: 1+ years |
We are looking to add a Development Associate I to our team for generating and documenting laboratory data with direct supervision. Your performance will contribute to a quality data generation in a regulated environment following good laboratory practices. | 05/19/2021 |
| 8672 | Vigene Biosciences Rockville, MD Research Associate I (Virus) Bachelor’s degree in biology, Cell Biology, Molecular Biology, or related field. Exp: 0-2 years |
As a part of Virus Production, the Research Associate is responsible for performing cell culturing, transfections, cell harvesting and purification with AAV and production procedures. | 05/19/2021 |
| 8673 | Vigene Biosciences Rockville, MD Research Associate I (Cloning) Bachelor’s degree in biology, Cell Biology, Molecular Biology, or related field. Exp: 0-2 years |
As a part of the Cloning team, the Research Associate is responsible for all aspects of DNA cloning projects involving digestion, ligation, and gel electrophoresis, also including organized record keeping and stock management | 05/19/2021 |
| 8674 | Charles River Laboratories Spencerville, OH Research Technician 1 *$1,000 sign-on bonus Bachelor’s/Master’s with no relevant experience. Exp: 0+ years |
We are seeking an experienced Research Technician for our Toxicology Team located in Spencerville, OH. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. The training and development offered to our entry level technicians is state of the art and designed to help you succeed. The work you will be doing will impact the lives of patients and animals across the world. | 05/19/2021 |
| 8675 | Charles River Laboratories Wayne, PA Technician 1 Microbiology Bachelor’s degree (B.S.) or equivalent in biology or a related discipline. Exp: 0 to 1 year |
We are seeking a Technician 1 Microbiology for our Biologics Testing Solutions site located in Wayne, PA. You may be required to work a rotating shift schedule that may require weekend hours. The responsibilities of this role as Technician 1 Microbiology will be specific to the Environmental Monitoring division of the Microbiology department. Daily activities and responsibilities of this role will include but are not limited to performance of environmental monitoring within cGMP general testing laboratories, and data entry. | 05/19/2021 |
| 8676 | Charles River Laboratories Horsham, PA Scientific Associate Minimum of a Bachelor’s degree (BA/BS) or equivalent in Toxicology, Pharmacology, or related discipline. Exp: No work experience required. |
This is an entry level trainee position for a Study Director/Scientist within the Safety Assessment division of Charles River Laboratories, Inc (CRL). A Study Director/Scientist has overall responsibility for the technical conduct of studies according to FDA or other applicable guidelines and Good Laboratory Practice (GLP) regulations. With guidance from senior scientific staff, serve as a Study Director in the direction and execution of assigned non-GLP and GLP studies as they apply to the conduct of preclinical research. In preparation to become a Study Director the objectives during this training period will be to ready the individual to be overall responsible of protocols/study plans, study schedules, Standard Operating Procedures and familiarity/awareness of study cost estimates. Overall interpretation of preclinical toxicity studies, evaluation and preparation of reports from the data collected during these studies, communication with sponsor representatives, initiating contact with potential clients, and may be involved with development of new technologies/procedures. | 05/19/2021 |
| 8677 | Charles River Laboratories Cleveland, OH Research Assistant 1 Bachelor’s degree (B.A. / B.S) or equivalent. Exp: Zero to two years |
We are seeking a Research Assistant I for our Safety Assessment Group site located in Cleveland, Ohio. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples, and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. | 05/19/2021 |
| 8678 | Charles River Laboratories Ashland, OH Research Assistant 1 (Analytical Chemistry) Bachelor’s degree (B.A. / B.S) or equivalent. Exp: Zero to two years |
We are seeking a Research Assistant I for our Safety Assessment Group site located in Ashland, Ohio. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples, and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. | 05/19/2021 |
| 8679 | Charles River Laboratories Ashland, OH Research Assistant 1 (Bioanalytical Chemistry) $1000 SIGN ON BONUS Bachelor’s degree (B.A. / B.S) or equivalent. Exp: Zero to two years |
We are seeking a Research Assistant I for our Safety Assessment Group site located in Ashland, Ohio. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples, and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. | 05/19/2021 |
| 8680 | Charles River Laboratories S. San Francisco, CA Research Associate, Bioanalytical Bachelor's degree (B.S./B.A.) or equivalent. Exp: Minimum 6 months |
We are seeking a Discovery Bioanalytical Research Associate (DMPK Bioanalytical) for our Discovery site located in South San Francisco, CA. We are seeking Research Associate candidates that are early in their careers and are highly motivated, enthusiastic and possess a passion for learning. This position will be involved in all aspects of studies supporting the bioanalysis of drug molecules in multiple matrices. This position is ideally suited to recent graduates who enjoy a fast-paced and collegial environment. The individual in this position will be responsible for working hands-on and under the direction of more senior staff in a dynamic environment where teamwork, data quality, innovation and speed are valued. | 05/20/2021 |
| 8681 | LabCorp S. San Francisco, CA Laboratory Technician - Entry level, will train! APPLY NOW BS/BA degree in Biology, Chemistry, Clinical Laboratory Science, or related scientific field Exp: Entry Level |
Monogram Biosciences, part of LabCorp, is seeking a Laboratory Technician to join its team in South San Francisco! This position will be responsible for working with automated and semi-automated equipment specifically working with cell-based assays from introduction of virus, cells and drug addition to the final read step. This is a great entry level opportunity to join an innovative laboratory and receive targeted one-on-one training that will help the individual grow in a career in the biotechnology field. The schedule for this position will be Monday -- Friday, 3pm-11:30pm with rotating weekends (one month on, one month off). Training will be: Monday-Friday, 6am-230pm for the first few months. | 05/20/2021 |
| 8682 | LabCorp Research Triangle Park, NC Cytogenetics Technologist Trainee - Entry level, will train! B.A./B.S. in Biology, Chemistry or related scientific discipline. Exp: Enrty Level |
The Integrated Genetics Division is seeking a Cytogenetics Technologist Trainee to join their Cytogenetics team in the Microarray Group! Assays performed in the Cytogenetics Department utilize a variety of scientific techniques, including specimen culturing, PCR, fragment analysis, and gel electrophoresis. Participate in LabCorp's in-house training program for the field of Cytogenetics. Receive in depth training and preparation for the ASCP board examination and ASCP-CG certification. Training program is a two year commitment. The schedule for this position is: Tuesday -- Saturday, 8am -- 4:30pm | 05/20/2021 |
| 8683 | LabCorp Burlington, NC Technologist Trainee - Chemistry (1sy Shift) Bachelor's degree in Biology, Chemistry, Medical Technology or a related science. Exp: 1 year |
LabCorp is seeking a Technologist Trainee to join our Chemistry lab team in Burlington, NC. The large range of assays within the department can be categorized into: General/Routine Chemistry, STD testing, Therapeutic Drug Monitoring, and Clinical Endocrinology, with the overall goal of providing results that can be used in the diagnosis and management of a wide range of illness and disease states. All of our assays are automated and our department includes some of the most advanced high-throughput analyzers available on the market. We are currently looking for individual(s) who are looking for an opportunity to get their career started and have the ability to grow within the company. The work schedule for this position will be Monday - Friday, 8:30 am - 5:00 pm. | 05/20/2021 |
| 8684 | KBI Biopharma Durham, NC Research Associate I/Research Associate II BS/MS in Chemistry, Biochemistry or Related Exp: 0+ Years |
Responsibilities: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. | 5/22/2021 |
| 8685 | KBI Biopharma Durham, NC Document Control Coordinator I/II BS/MS in Relevant Scientific Discipline Exp: 1-2 Years |
Responsibilities: Performing review of cGMP documents in EtQ in preparation for Department/Technical, QA, and client (if applicable) review and approval. Controlling issuance, receipt, and archival of cGMP documentation. Communicating with the client regarding document review and approval and updates to the cloud, if applicable. Maintaining controlled forms (logbooks, etc.) for applicable departments. Fulfilling documentation requests from internal and external customers, including client audits and regulatory inspections | 5/22/2021 |
| 8686 | KBI Biopharma Boulder, CO Manufacturing Systems Analyst BS in IT or Relevant Scientific Discipline Exp: 1-4 Years |
The Manufacturing Systems Analyst will be required to resolve routine requests that may include project/folder creation, system backups, account requests, etc.; as well as troubleshooting and resolution of complex issues related to Manufacturing Systems. The position will require the interaction with end users to ensure that all end-user requests are fulfilled and issues are resolved in a timely manner. The Manufacturing Systems Analyst must be customer focused and a good communicator.The Manufacturing Systems Analyst will be required to serve as the Subject Matter Expert (SME) on Projects relating to the installation, validation and deployment of laboratory and manufacturing systems. The position requires basic knowledge of the Computer Systems Validation (CSV) process and will assist in the writing and execution of CSV deliverables as required. | 5/22/2021 |
| 8687 | KBI Biopharma The Woodlands, TX QC Analyst MS in Life Sciences Discipline Exp: 1 Year |
Responsibilities: This individual will conduct cell culture and bioassays in support of in process testing, product characterization and potency assessment. Requirements of the position include execution and documentation of experimental protocols and assisting in the qualification and validation of methods. Execute multiple laboratory procedures such as primary and immortalized cell culture (aseptic technique), determination of cell number and viability, cytokine detection assays, multi-color flow cytometry, and qRT-PCR. Interpret and follow standard operating procedures and execute activities in accordance with cGMP, GLP, regulatory, and safety requirements as directed. Independently trouble-shoot and report results. Assist in qualification and validation of methods to support product characterization. Participate in organization, supply maintenance, and record keeping duties as needed to support the laboratory. | 5/22/2021 |
| 8688 | KBI Biopharma Durham, NC Manufacturing Associate I/ II-Upstream BS in Relevant Science or Engineering Discipline Exp: 0-2 Years |
The candidate will maintain a sense of ownership of the production processes, manufacturing environment and facility. They will be exposed to cell culture media preparation, shake flask operations, seed expansion, bioreactor setup and operations, cell culture harvest setup and operations, and aseptic technique; as well as to cell culture analytical tools and general biotechnology auxiliary equipment (pumps, sterile tubing welders and sealers, pH/Conductivity/osmolarity meters). Following task execution, the Manufacturing Associate I/II will review the executed production records (SR's, ERP, and BR's) to ensure GxP compliance. | 5/22/2021 |
| 8689 | KBI Biopharma Durham, NC Sr. Manufacturing Associate I/II-Downstream BS in Relevant Science or Engineering Discipline Exp: 0+ Years |
Responsible for a wide variety of cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Follow SOPs, perform daily tasks in a clean-room, retain records and writereports. May also be responsible for troubleshooting. | 5/22/2021 |
| 8690 | KBI Biopharma Boulder, CO Research Associate/Sr. Research Associate BS in Relevant Scientific Discipline Exp: 0-2 Years |
The new associate will actively participate in a dynamic laboratory environment, learning cutting-edge analytical techniques, developing data analysis tools, establishing direct relationships with clients, and continuing to build a world-class specialty analytical business. | 5/22/2021 |
| 8691 | Keros Therapeutics Lexington, MA Research Project Manager, Nonclinical Operations BS/MS in Relevant Scientific Discipline Exp: 0+ Years |
This role will have hands-on responsibility for assisting in the technical conduct of a wide range of Nonclinical Safety Studies, from discovery through development Projects. The Research Project Manager will contribute to the Nonclinical Safety program activities, including short- and long-term planning, budgeting and managing expense priorities, SOP development, archival retention, process improvements, and study tracking. This position will also contribute to the conceiving, developing, managing, directing, and organizing activities for study coordination and assist in the development of nonclinical safety studies. The incumbent should have basic knowledge of drug development principles, drug safety testing and regulatory guidelines. This position will report to the Head of Nonclinical Safety. | 5/22/2021 |
| 8692 | Keystone Nano State College, PA Research Chemist MS in Biochemistry, Bioengineering, Chemical Engineering, Materials Science or Related Exp: 0+ Years |
Keystone Nano is looking for a Research Chemist able to play an important role in developing novel drug products for cancer applications. The successful candidate will join their laboratory in State College, PA to conduct chemical and physical experiments using proprietary manufacturing techniques to develop and scale this technology for a variety of markets. | 5/22/2021 |
| 8693 | Keystone Nano State College, PA Research Technician BS in Biochemistry, Bioengineering, Chemical Engineering, Materials Science or Related Exp: 0+ Years |
Keystone Nano is looking for a Research Technician able to play an important role in developing novel drug products. The successful candidate will join their laboratory in State College, PA to expedite work flow and maintain a positive team environment. | 5/22/2021 |
| 8694 | Kezar Life Sciences San Francisco, CA Sr. Research Associate, Pharmaceutical Development MS in Chemistry, Pharmaceutical Sciences, or Related Exp: 0+ Years |
The position reports to the Scientist, Pharmaceutical Development and will develop preclinical and clinical formulations, and the analytical methods to characterize them, in support of small molecule immunology and oncology programs. The successful candidate will be part of a dynamic, interdisciplinary team requiring a high degree of creativity and initiative. | 5/22/2021 |
| 8695 | Kiniksa Lexington/San Diego, MA Clinical Trial Associate BS in Relevant Scientific Discipline Exp: 1-2 Years |
Reporting to the Associate Clinical Project Manager, the Clinical Trial Associate (CTA) will be tasked with providing clinical trial coordination support, along with implementing the clinical operational plans in accordance with regulatory guidelines and ICH/GCP standards. The CTA will be responsible for providing Clinical Operations support of study specific reports and site and vendor management activities. | 5/22/2021 |
| 8696 | Kite Cell Therapy El Segundo, CA Cell Therapy Specialist BS in Relevant Scientific Discipline Exp: 1+ Years |
Kite is seeking a highly motivated individual with cell culture experience to work on innovative T cell therapy for cancer treatment. The Cell Therapy Specialist will be responsible for cell culture media preparation, cell processing and cell expansion in a cGMP manufacturing facility. | 5/22/2021 |
| 8697 | Kite Cell Therapy El Segundo, CA Process Engineer, Manufacturing Sciences & Technology MS in Biochemical Engineering, Chemical Engineering, Biotechnology, Chemistry, Biology, or Equivalent Exp: 0+ Years |
As a Process Engineer for Manufacturing Sciences and Technology (MSAT), you will provide process science support for commercial GMP manufacturing, technology transfers, development studies, validation, and continuous improvement projects for Kite’s engineered T cell therapy products. Additionally, you will write product impact assessments, root-cause analysis reports, sampling plans, technical reports, and provide technical assessments, rationales and approval for engineering and process changes as well as documentation pertaining to process development, qualification, and validation to meet regulatory requirements. | 5/22/2021 |
| 8698 | Kite Cell Therapy Frederick, MD Maintenance Technician MS in Relevant Science or Engineering Discipline Exp: 0+ Years |
This position will provide support to the facilities and engineering team and assist in the operation and maintenance of the company’s facility and equipment for production of cell-based therapeutics. | 5/22/2021 |
| 8699 | Korro Bio Cambridge, MA Associate Scientist, Bioinformatics MS in Computer Science, Cheminformatics, Bioinformatics or Related Exp: 1-2 Years |
Responsibilities: Design and implement data workflows to automate the data extraction, transformation and loading from the high-throughput screening experiments. Create the dashboards to summarize and visualize the results of high throughput screening experiments. Manage data in the compound database and laboratory information systems. Develop, operate and maintain data process pipelines and cloud applications. | 5/22/2021 |
| 8700 | Korro Bio Cambridge, MA Associate Scientist, Cell Biology MS in Molecular/Cellular Biology Exp: 1-2 Years |
Responsible for the design, execution and analysis of a variety of in vitro cellular and molecular based assays, focused on understanding and optimizing a ADAR-mediated RNA editing platform. | 5/22/2021 |
| 8701 | Krystal Biotech Pittsburgh, PA GMP Manufacturing Associate BS in Relevant Scientific Discipline Exp: 1+ Years |
Responsibilities: Develop and execute SOPs. Execute and report IQ/OQ for equipment. Operate and maintain manufacturing equipment. Perform process for manufacturing drug product for clinical trials. Clean and maintain GMP facility. Engage with process development team for tech transfer of improvements/scale up. | 5/22/2021 |
| 8702 | Krystal Biotech Pittsburgh, PA Research Associate, Analytical Development BS/MS in Biology, Biochemistry, Chemistry, or Related Exp: 0-2+ Years |
Krystal Biotech, Inc is seeking a highly motivated Research Associate to perform high quality analytical development to support research for gene therapy products. This position will be laboratory based. | 5/22/2021 |
| 8703 | Kymera Therapeutics Watertown, MA Senior Research Associate/Research Associate, Oncology Biology MS in Biology, Molecular Biology, Biochemistry, or Related Exp: 0+ Years |
The experienced Senior Research Associate/Research Associate will be responsible for providing biology support to one or more projects and help drive Kymera programs toward the clinic. The successful candidate will be able to work independently within a highly interactive environment, exhibit strong attention to details, and possess excellent record keeping and organizational skills. They will be expected to generate high quality data and analyze and communicate the results to project team members. | 5/22/2021 |
| 8704 | Kymera Therapeutics Watertown, MA Senior Research Associate/Research Associate, In Vivo Pharmacology BS/MS in Relevant Scientific Discipline Exp: 1-3 Years |
Kymera is seeking a highly motivated Senior Research Associate/Research Associate, in vivo Pharmacology to support our discovery and development efforts. The successful candidate will be required to execute all aspects of pre-clinical in vivo studies including dosing, tissue collection and data analysis, to advance their preclinical research. This individual should have extensive hands-on experience with in vivo procedures in rodents. | 5/22/2021 |
| 8705 | Kymera Therapeutics Watertown, MA Lab Technician BS in Relevant Scientific Discipline Exp: 0+ Years |
Responsibilities: Ordering, receiving and stocking laboratory consumables, organization and maintenance of Lab. Cold-chain shipping. Manage weekly deliveries of Dry Ice and Gases. Replenish bench consumables and Manage biohazards. Assist with equipment maintenance (ie weekly de-icing of freezers), reagent changes, and removal of solvent collections. Assist research staff in maintaining and overseeing the general laboratory environment including cleanliness of space, organization of stock materials and order preparation. Prepare and maintain stocks of common reagents in the laboratory. | 5/22/2021 |
| 8706 | Lannett Seymour, IN Drug Product & Stability Chemist BS in Chemistry or Related Exp: 0+ Years |
This position is primarily responsible for the laboratory testing of in-process, release and stability samples for commercial drug products. | 5/22/2021 |
| 8707 | Lannett Seymour, IN Technical Services Scientist I BS in Relevant Scientific Discipline Exp: 0-4 Years |
This position is viewed as a technical resource in process development and/or daily commercial support. A Technical Services Scientist understands and applies technical principles, theories, and concepts in solid dosage manufacturing. The scientist will apply technical knowledge, creativity, and company practices under supervision and directions from the management to support the new process development through commercial launch, commercial manufacturing support throughout product life cycle, technology transfers and process improvement/optimization activities while meeting project time lines. | 5/22/2021 |
| 8708 | Legend Biotech Raritan, NJ QC Analyst BS in Relevant Science or Engineering Discipline Exp: 1+ Years |
The QC Analyst, CAR-T Manufacturing is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. | 5/22/2021 |
| 8709 | LGC Charleston, SC Production Chemist BS in Chemistry or Related Exp: 0+ Years |
This is a production job in which the chemist is expected to produce standards quickly and accurately using weighing, syringing, and pipetting techniques. Packaging is also involved which includes putting products in bottles, ampules, or another specified container and applying labels for clients. | 5/22/2021 |
| 8710 | LGC Petaluma, CA Oligonucleotide Production Technician BS in Life Sciences or Chemistry Exp: 0+ Years |
The Oligo Production Technician I is responsible for performing day to day production activities in the custom oligonucleotide (oligo) production lab. Production activities will be performed in a timely fashion and in compliance with company procedures. | 5/22/2021 |
| 8711 | LGC Petaluma, CA Process Development Chemist BS/MS in Chemistry, Chemical Engineering or Related Exp: 1+ Years |
LGC is looking for highly a motivated chemist, biochemist and/or chemical engineer to join in their newly commissioned state-of-art therapeutic oligonucleotide GMP manufacturing facility in Petaluma, CA. This individual will work in a Process Development lab to support therapeutic oligonucleotide manufacturing process development, transfer and trouble-shooting production issues. | 5/22/2021 |
| 8712 | LGC Manchester, NH Analytics Laboratory Manager BS/MS in Physical Science or IT Exp: 0+ Years |
This role requires and individual with background in analytics and managing data; however will also have a laboratory management role to oversee groups tasked with providing the measurement data as well as document generation. Position is a new role for developing the integration of data streams from multiple analytical instruments, as well as internal manufacturing department data, carry out-processing using common statistical methods and oversee its transfer into reports. It is an impactful position that is well suited for an individual with a background in data integration and computer skills to apply to a range of non-routine analytical chemistry applications for materials and other industrial samples. Position will initially work alongside company ERP system, but longer term to develop LIS software that may require considerable customization; hence, light programming experience is desirable. | 5/22/2021 |
| 8713 | LGC Lexington, KY Program Coordinator BS in Relevant Scientific Discipline Exp: 0+ Years |
Responsibilities: Ensure that all relevant program documentation and sample testing has been completed with satisfactory results to allow certification of products, raw materials and sites. Generate and issue certificates to Members upon completion of certification. Work cohesively with Program Management colleagues to monitor and maintain the certification process; communicating with operational colleagues to ensure efficient processing of samples through the laboratory. Track blind sampling, ensuring samples are purchased and submitted in line with program requirements. Assist in the ongoing management of all certified products, raw materials and sites, ensuring compliance against program requirements (including Manufacturer re-reviews and Member reviews). | 5/22/2021 |
| 8714 | LGC Novato, CA Instrumentation Technician BS in Relevant Scientific Discipline Exp: 0+ Years |
The Instrumentation Technician is responsible for maintenance and repair activities associated with the Oligonucleotide manufacturing equipment. This includes creating documentation for maintenance activities, performing the maintenance activities, and training production staff to perform maintenance activities. Responsibilities will also include recommending and implementing improvements to the system. This position will report on the status and key metrics of the equipment. | 5/22/2021 |
| 8715 | LGC Lexington, KY Quality, Safety, Health and Environmental Associate BS in Relevant Scientific Discipline Exp: 0+ Years |
The purpose of this role is to provide support to the QSHE functions in Lexington, ensure compliance with regulatory guidelines and to help manage the QSHE systems. The QSHE associate will engage with members of other teams in Lexington as well as other teams from various LGC locations and may engage with customers. | 5/22/2021 |
| 8716 | Lifecore Biomedical Chaska, MN Associate Design Engineer BS in Relevant Science or Engineering Discipline Exp: 0-2 Years |
This individual will provide quality engineering support for assigned efforts, such as new product implementation, commercial production support and quality system improvements. They will support assigned teams to generate product quality system documentation, ensure high process capability outcomes, and generate risk management documentation. Additionally, they will support process, equipment, software, and facility validation protocol generation, execution, and report generation. | 5/22/2021 |
| 8717 | Lipocine Salt Lake City, UT Product Development, Associate Scientist BS/MS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or Related Exp: 1-3 Years |
Responsibilities: Under minimal/no supervision develop and validate analytical methods to support product development, release testing and stability activities for pharmaceutical drug product programs. Perform physical and chemical tests on active pharmaceutical ingredients, raw materials, in-process, and finished products using various wet chemical, physical and instrumental techniques. Hands on experience with HPLC/UPLC with various detectors, related spectroscopy, KF (Karl Fisher), dissolution, and other common analytical methods. Conduct laboratory experiments in support of formulation and process development. Assist/perform manufacturing preclinical formulations and early clinical supplies. Generate and collate the data, perform required calculations and document experiments and results in a laboratory notebook following GMP/GLP practices. | 5/22/2021 |
| 8718 | Locus Biosciences Research Triangle Park, NC Development Specialist or Scientist BS/MS in Biology, Chemistry, Biochemistry, Chemical Engineering, Biophysics, Pharmaceutical Technology or Related Exp: 0+ Years |
Locus Biosciences has an immediate need for a highly motivated and experienced applicant to join their team as a full-time Development Specialist or Development Scientist responsible for developing biologics purification processes and formulations, as well as supporting early phase clinical trial material manufacturing in an aseptic environment. This position is well suited for those that have demonstrated laboratory experience, with solid communication, technical aptitude and problem-solving skills. | 5/22/2021 |
| 8719 | Locus Biosciences Research Triangle Park, NC Translational Medicine Research Technician BS in Relevant Scientific Discipline Exp: 1-5 Years |
Locus Biosciences is seeking highly motivated applicants to join their research and development team as a full-time Research Technician within the Translational Medicine group. This position is well-suited for highly motivated technicians that have a desire to push product development forward into critical preclinical in vitro and in vivo testing across a variety of therapeutic indications. This individual will work directly with scientists in both Development Translational Medicine as well as the Discovery group to develop and execute in vivo animal models and analyze tissue samples using various molecular and biochemical assays. The ideal candidate will be well organized and have a scientific background as well as experience with microbiology techniques and in running animal models. | 5/22/2021 |
| 8720 | Locus Biosciences Research Triangle Park, NC Project Manager BS/MS in Biology, Biochemistry, Genetics, or Related Exp: 0+ Years |
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join their team as a full-time R&D Project Manager responsible for developing, maintaining and executing research plans across Locus Biosciences. The incumbent will be able organize and drive projects across Locus Biosciences to completion, including cross-departmental projects spanning the drug development pipeline. This role requires an ability to interact with technical staff and consistently translate drug development activities across our teams into visible project plans. This person will be responsible for managing detailed project plans across multiple programs, including developing and updating Project Gantt charts, leading status update meetings, and ensuring good cross-team communication. | 5/22/2021 |
| 8721 | LogicBio Lexington, MA Research Associate, Process Analytics BS in Cell Biology, Biochemistry, Molecular Biology or Related Exp: 1-2 Years |
LogicBio is seeking a research associate to join their Process Analytics team within the Technology Development group. In this position, the successful candidate will follow established standard operating procedures (SOPs) to perform molecular and biochemical based assays to characterize recombinant adeno-associated viral (rAAV) vectors to support process development and testing of pre-clinical grade research products. | 5/22/2021 |
| 8722 | LogicBio Lexington, MA Research Associate/Senior Research Associate Gene Therapy BS in Biology, Biochemistry or Related Exp: 1-3 Years |
LogicBio is seeking a highly motivated team member who will assist the team with the in vitro and in vivo assays related to developing gene therapy products. Specifically, the successful candidate will be involved in maintenance, expansion and banking of cell culture lines, in vitro and in vivo analytical and functional bioassays for characterizing internal and external AAV vector product, molecular quantification assays, potency assessment and biodistribution studies. | 5/22/2021 |
| 8723 | LogicBio Lexington, MA Research Associate/Senior Research Associate, Vector Production BS in Engineering, Biotechnology, Biology, Biochemistry, Virology or Related Exp: 1-3 Years |
LogicBio is seeking a highly motivated and scientifically rigorous individual to join their Vector Development and Operations group at either the Research Associate or Senior Research Associate level. This position will focus on developing research vector production methods, vector analytical methods and producing pre-clinical material. | 5/22/2021 |
| 8724 | Cell Signaling Technology Beverly, MA Research Associate I - Tissue Culture Core Bachelor’s degree in a biological science (e.g. molecular biology, cell biology, biochemistry or biotechnology) Exp: 0-1 years |
The TCC team is responsible for maintaining a reliable cell line bank and generating high quality lysates for the CST Production department. | 5/10/2021 |
| 8725 | Repligen Waltham, MA Manufacturing Associate I - OPUS BS degree. Exp: 0- 3 years’ |
Experience working in a classified cleanroom, and knowledge of GMP/ISO/document controlled processes would be beneficial. Attention to detail, and the ability to work in a team environment are essential. Ability to read engineering drawings and be familiar with process control software is also highly desirable. | 5/10/2021 |
| 8726 | Repligen Waltham, MA Manufacturing Associate I - ELISA (1st Shift) Requires an AS/BS or equivalent. Exp: 0 - 2 + years |
The successful candidate will be responsible for the manufacture of ELISA kits and its components as well as in-process testing. The individual must be able to follow oral and written instructions accurately and complete tasks in a timely manner. | 5/10/2021 |
| 8727 | WuXi Apptec Marietta, GA Laboratory Technician Associate or Bachelor’s Degree in Chemistry or equivalent experience. Exp: 1-2 years |
We have an opening in our Chemistry Department for an Associate Lab Technician. Perform following test methods: Karl Fischer, Heavy Metals, Pchem, Seal, Peel, Burst testing. | 05/10/2021 |
| 8728 | WuXi Apptec Natick, MA HitS DEL Biology Scientist B.S./M.S. degree in biochemistry, molecular biology, biotechnology or related discipline. Exp: 1-3 years |
DEL (DNA-encoded library) is a rapidly growing drug discovery platform at HitS Business Unit in WuXi AppTec. This cutting-edge multidisciplinary platform combines the latest technologies in chemistry, chemical biology, biology and informatics. | 05/10/2021 |
| 8729 | WuXi Apptec Philadelphia, PA Laboratory Technician I, Microbiology (M-F, 2nd shift) Bachelors degree in Biological Sciences or or other science-related major. Exp: 0-1 years |
The Laboratory Technician will performs basic protein based assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). | 05/10/2021 |
| 8730 | WuXi Apptec Cranbury, NJ Associate Scientist I Bachelor’s degree in animal science, biology, or a related discipline. Exp: 0-3 years |
Plans and carries out quantitative whole body autoradiography (QWBA) experiments and associated research assignments. Operates lab equipment including microtome and scanners. Performs introductory tissue distribution estimates for QWBA images. Participates on in vivo experiments on rodents as required. | 05/10/2021 |
| 8731 | WuXi Apptec Plainsboro, NJ IT Technical Support Specialist I Associate’s or Bachelor’s degree. Exp: 1-2 years |
Responsible for first level day to day onsite support of users and systems (regulated and non-regulated). | 05/10/2021 |
| 8732 | WuXi Apptec Philadelphia, PA Laboratory Technician II Bachelors’ degree in Biological Science or other related science field. Exp: 1-2 years |
Performs Cell Culture, qPCR and Cell-Based assays (BSL2 and BSL2+) according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR)... | 05/11/2021 |
| 8733 | WuXi Apptec Philadelphia, PA Laboratory Technician II, QC Analytical (M-F 1 shift) Bachelor’s or Master’s degree with major in Biological Sciences or other science-related major. Exp: 1-3 years |
Performs basic and next-level Analytical assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). | 05/11/2021 |
| 8734 | Caribou Biosciences Berkeley, CA Sequencing Research Associate B.Sc. or equivalent in Biochemistry, Bioengineering, Molecular Biology, or a related field. Exp: 1-2 years |
We are seeking a Sequencing Research Associate to join our Molecular Engineering group. In this role, you will run and maintain a custom sequencing and genomic detection pipeline. The ideal candidate will interact closely with Scientists and other RAs to support sequencing and cell-based screening activities and will participate in the design and implementation of automated workflows. | 05/11/2021 |
| 8735 | Catamaran Bio Cambridge, MA Research Associate/Sr Research Associate, Cell Process BS or MS in bioengineering, chemical engineering, biochemistry, chemical biology, biology, biophysics, pharmaceutical sciences, or equivalent/related Exp: 1-5 years |
Catamaran is seeking an experienced, hands-on Senior Research Associate / Research Associate to join the development team in assembling a state-of-the-art manufacturing process for our allogeneic NK cell drug product. The successful candidate will be responsible for optimizing our cell processes for NK cells, including cell isolation, engineering, expansion, harvest and cryopreservation. | 05/11/2021 |
| 8736 | Catamaran Bio Cambridge, MA Research Associate/Sr. Research Associate, In vivo tumor immunology BS/MS with 0-2 years (RA level) Exp: 0-2 years |
Catamaran Bio is seeking a highly motivated, experienced, and creative individual with expertise in mouse in vivo tumor efficacy studies to contribute to our research efforts to advance our best-in-class Immune Cell Therapies for Oncology. This individual will be responsible for carrying out in vivo pharmacology studies, through preclinical studies to IND submission. | 05/11/2021 |
| 8737 | Concuir Consulting Orange County, CA ASSOCIATE CONSULTANT – ENGINEER I/II BS degree. Exp: 1+ years’ |
As a full-time employee of Concuir, Inc, you will provide consulting services to pharmaceutical, biotech and/or medical device clients. In this role, you will quickly learn client typical practices and be in a position to recommend and implement improvements to reach project goals. This is based on your experience as well as from Concuir’s portfolio of project management and cGxP best practices. Typical projects range from design through qualification of production equipment and/or utilities to modification or implementation of new facilities and process scale ups. | 05/13/2021 |
| 8738 | CovalX Saugus, MA ENTRY LEVEL FIELD/LAB ENGINEER BSc degree or equivalent Mechanical, Chemical, Electrical Engineering or Life/Analytical Science. Exp: entry level |
This position will offer the opportunity for an entry level person to get hands on experience with some of the most cutting edge analytical instrumentation located in the world's best research labs. The position will involve completing final assembly and testing of our high mass MALDI detector systems, followed by installation of these systems at customer sites. Due to the novelty of many of the required tasks, training will be provided by CovalX. | 05/13/2021 |
| 8739 | Crinetics Pharmaceuticals San Diego, CA Research Associate, CMC Analytical A bachelor’s or master’s degree in analytical chemistry or related field. Exp: 1 year |
Crinetics Pharmaceuticals is seeking a highly motivated professional to perform analytical functions for active pharmaceutical ingredients (API) and drug product (DP), joining its growing and dynamic team. This job will report to the Director, CMC Analytical. The Chemistry, Manufacturing and Controls (CMC) team is highly collaborative with a global network of highly qualified Contract-Research Organizations (CROs) and Contract Development and Manufacturing Organizations (CDMOs). This individual will be an integral part of the company’s effort to discover and develop small molecule therapeutics for rare endocrine disorders and endocrine-related-tumors. | 05/13/2021 |
| 8740 | CTK Biotech Poway, CA QC Assistant BS or AA in biological science or equivalent experience. Exp: 1 year |
The QC Assistant is responsible for inspecting and reporting on material processes and products; performing and documenting visual, dimensional and functional inspection of in-coming raw material, intermediate material and finished product; responsible for some QA related work for maintaining and improving the quality management system. | 05/13/2021 |
| 8741 | Decipher Biosciences San Diego, CA Clinical Lab Technician Bachelor’s degree required. Exp: 1 years’ |
The Clinical Lab Technician’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. | 05/13/2021 |
| 8742 | Deepcell Mountain View, CA Research Associate Bachelor’s or Master’s degree in Bioengineering, Biomedical Engineering, or similar subject is required. Exp: one year |
Operate and maintain lab instruments including Deepcell R&D systems Troubleshoot and optimize components related to Deepcell’s microfluidic cell analysis workflow Perform cell culture and blood processing protocols Improve upon existing SOPs and develop new SOPs with consistency and clarity Execute standard molecular biology techniques | 05/13/2021 |
| 8743 | DermTech San Diego, CA Research Associate - Diagnostics B.S. in biological sciences. Exp: 1+ years |
An integral part of the R&D team, the Research Associate (RA) will have the opportunity to work with the team to explore new technologies and assist in the development of molecular diagnostic tests in DermTech’s current and future product pipeline. The RA will conduct laboratory tests that generate high-quality data to support the development of molecular diagnostic tests. | 05/13/2021 |
| 8744 | DermTech San Diego, CA Research Associate/Scientist Bachelor degree with relevant experience in Biology, Immunology, Molecular Biology, Genetics, Biochemistry, or related field is preferred. Exp: 1 - 5 years' |
The Research and Development team at DermTech is seeking a Research Associate (RA) to collaborate on biomarker research, discovery, and validation in dermatological diseases. The successful candidate will join a research team that combines cutting-edge proteomic and genomic approaches to interrogate and characterize inflammatory pathways involved in the pathogenesis of dermatological disease. Specifically, the candidate will explore and incorporate new technologies in support of molecular diagnostic development. | 05/13/2021 |
| 8745 | DemTech San Diego, CA Medical Laboratory Technician BS in Medical Technology, Biology, Chemistry Microbiology or related area. ASCP MLT Certification. Exp: 0-2 years |
Reporting to Laboratory Manager, under supervision of licensed personnel, the MLT will prepare samples in the pre-Analytical phase to be processed by the CLS and functions as support for other laboratory functions. | 05/13/2021 |
| 8746 | Dewpoint Therapeutics Boston, MA RA/Sr. RA – Chemical Biology B.S. or M.S. in Biochemistry, Chemical Biology, Chemistry, Molecular Biology or a related field. Exp: 0-3+ years |
We are searching for a creative and experienced Research Associate or Senior Research Associate to help build Dewpoint’s novel technology platform. You will play a pivotal role in developing and executing cellular and biochemical assays to characterize disease-relevant condensates, and to discover novel condensates with critical roles in disease. | 05/14/2021 |
| 8747 | DiabetOmics Hillsboro, OR Research Assistant/Associate in Product Development (2 positions available immediately) BA/BS in a relevant biological science. Exp: 1-2 years |
Diabetomics, Inc., is a leading medical diagnostics company serving the needs of personalized health and diabetes risk assessment and management. Diabetomics R&D group is currently seeking a Research Assistant/Associate to join our established team. Essential Functions: Supports the Diagnostic Product Development team. This is a hands-on, bench-level laboratory position. Tasks will include, but are not limited to: assay feasibility, assay development, optimization, reagent formulation, verification and validation studies. | 05/14/2021 |
| 8748 | Dicerna Pharmaceuticals Lexington, MA Research Associate, Chemistry B.S. or M.S. in Chemistry. Exp: 1-3 years’ |
Dicerna Pharmaceuticals is seeking a highly motivated Research Associate with a strong background in synthetic and medicinal chemistry to join the Chemistry Team. The candidate will be responsible for the synthesis of oligonucleotide conjugates, nucleoside analogues, small molecule ligands, and linkers. This position will contribute to the development of novel nucleic acid conjugate platforms and support therapeutic programs in multiple disease areas. | 05/14/2021 |
| 8749 | Discovery Life Sciences Huntsville, AL Laboratory Associate - Cell Processing Bachelor's degree in molecular or cell biology, biochemistry or be an MLT. Exp: 1-3 years |
Discovery Life Sciences is a trusted provider of bioanalytic and biospecimen services to hundreds of customers across the U.S. and around the world. We're looking for a Laboratory Associate for our Cell Processing lab to work 2nd shift, who will process biospecimen samples for cryopreservation or further characterization based on standard operating procedures. | 05/14/2021 |
| 8750 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 05/14/2021 |
| 8751 | DxTerity Rancho Dominguez, CA Molecular Clinical Laboratory Scientist BA, BS, or MS in Molecular Biology, Genetics, or related life sciences field. Exp: 1-4 years |
Valid California CLS license (generalist or CGMBS) is required. California-licensed Clinical Laboratory Scientist (CLS) specializing in molecular biology techniques, responsible for performing and maintaining high complexity laboratory testing on patient specimens, interpreting and reporting patient results, performing quality control and quality assurance procedures, and complying with all applicable local, state and federal laboratory requirements. | 05/14/2021 |
| 8752 | DxTerity Rancho Dominguez, CA Research Associate A B.S. or M.S Degree in Biochemistry, Molecular Biology or a related field Exp: 1-3 years |
DxTerity, a patient-centric genomics company located in Los Angeles, CA is looking to hire a Research Associate to join our Research and Product Development team. Responsibilities include: development of molecular diagnostic test kits, reagents and procedures in a team environment. Perform experiments independently after receiving general direction from supervisor. Make detailed observations, analyzes data and interpret results. | 05/14/2021 |
| 8753 | Evelo Biosciences Cambridge, MA Microbiology Research Associate BS or MS degree in microbiology or related field. Exp: 1 year |
We are looking for a Research Associate to join our Microbiology group to help drive key programs. This exciting role will afford a qualified Research Associate the opportunity to apply their extensive knowledge of microbiology to perform experiments that will aim to cultivate a broad variety of aerobic and anaerobic bacteria, and characterize their molecular, morphological, and physiological features. The successful candidate will possess the required skills in microbial physiology, maintenance and preservation, microscopy, molecular methods, formulation of media composition, and the ability to multi-task within scope. | 05/14/2021 |
| 8754 | Ionis Pharmaceuticals Carlsbad, CA Automation Scientist/Research Associate - Lead Identification Group, Antisense Drug Discovery BS in Biology or Related Exp: 1+ Years |
Ionis is seeking a highly motivated and outstanding individual to join the Antisense Lead Identification group as an Automation Scientist/Research Associate. The selected candidate will work alongside a Senior Automation Scientist in the development and execution of a state-of-the-art high throughput automation workflows to serve drug discovery and lead Identification needs. The successful candidate is expected to be self-motivated and able to work productively in a team environment as well as independently. The applicant should have a strong desire to apply their biological sciences background in an automated high-throughput environment. | 5/15/2021 |
| 8755 | Ionis Pharmaceuticals Carlsbad, CA Manufacturing Research Associate BS in Chemistry, Chemical Engineering, Biology, or Related Exp: 1+ Years |
Responsibilities: Synthesize and isolate synthetic oligonucleotides using automated equipment in a cleanroom environment. Operate equipment from laboratory scale to large production scale. Formulate reagent and buffer solutions following standard operating procedures (SOPs) in accordance with current good manufacturing practices (cGMPs). Investigate process improvements and scale-up methods. Perform cleaning of production equipment following established SOPs. Document cGMP production activities by completing all forms, reports and records. Develop Standard Operating Procedures and manufacturing documents for process and equipment operation. | 5/15/2021 |
| 8756 | Ionis Pharmaceuticals Carlsbad, CA Research Associate, Analytical Development & Quality Control BS in Relevant Scientific Discipline Exp: 0+ Years |
Responsibilities: Responsible for performing and reviewing quality control release testing for in-process intermediate samples, drug substances (DS) and drug products (DP) according to standard operating procedures. Initiate and manage DS and DP stability programs and perform routine stability testing for DS and DP in compliance with SOPs, cGMP and regulatory requirements. Communicate with domestic and international external test labs, resolve any conflicts, and facilitate: the shipping and receiving of samples, expedited testing and obtaining results reports for release and stability testing. Review external result reports for accuracy, completeness and compliance against established standards. Compile and review analytical GMP data for compliance to specification and test procedures. Assess analytical data and if applicable initiate records and documentation for: no-tests, system suitability failures, deviations and CAPAs when necessary. Also, perform OOT/OOS analytical investigations. | 5/15/2021 |
| 8757 | Ionis Pharmaceuticals Carlsbad, CA Clinical Trial Master File Manager BS/MS in Relevant Scientific Discipline Exp: 0+ Years |
The Clinical Trial Master File (TMF) Manager is responsible for eTMF quality as per GCP/ICH guidelines for all Ionis sponsored clinical trials (domestic and multi-national). This manager position will manage the document control processes and systems for GCP activities in compliance with Ionis internal procedures and policies, review suitability of documentation for filing, maintain the TMF records including storage, retrieval, retention, and destruction per Ionis SOPs. This position serves as the main contact with the project teams and cross functional departments. The manager will plan and perform internal periodic quality checks, provide support to the clinical teams during regulatory inspections for record organization and retrieval, be the subject matter expert for the TMF process, develop and provide training to those requesting access to the TMF, and provide metrics to the team. This position will also manage direct reports. | 5/15/2021 |
| 8758 | Ionis Pharmaceuticals Carlsbad, CA Research Associate/Senior Research Associate, Receptor Biology BS in Cell Biology, Biochemistry, Molecular Pharmacology or Related Exp: 0+ Years |
Incumbent will be an integral member of Medicinal Chemistry helping to design, express, purify and characterize protein ligands and reagents for oligonucleotide conjugation. | 5/15/2021 |
| 8759 | Ionis Pharmaceuticals Carlsbad, CA Scientist/Research Associate, Medicinal Chemistry BS/MS in Organic Chemistry, Biochemistry, or Analytical Chemistry Exp: 0-2 Years |
Ionis is looking for a motivated individual to join their Oligo Synthesis / Medicinal Chemistry group. Candidate will assist with high throughput synthesis of oligonucleotides on 1 – 2 µmol scale. The candidate will also provide synthetic support to the Medicinal Chemistry group including the synthesis and purification of oligonucleotides, oligo precursors, and oligo conjugates. | 5/15/2021 |
| 8760 | Ionis Pharmaceuticals Carlsbad, CA Scientist/Research Associate – Lead Identification Group, Antisense Drug Discovery BS in Biology or Related Exp: 1-4 Years |
Ionis is seeking an enthusiastic and highly motivated individual to join the Antisense Lead Identification group as a Scientist/Research Associate. The successful candidate will work within a fast-paced, highly productive, and innovative research team responsible for the antisense oligonucleotide therapeutic in vitro lead identification. The successful candidate is expected to be self-motivated and able to work productively in a team environment as well as independently. The applicant should have a strong desire to apply their biological sciences background in an automated high-throughput environment. Ionis cultivates a work environment with many opportunities to learn in R&D and encourage all highly motivated candidates to apply. | 5/15/2021 |
| 8761 | Iovance Biotherapeutics Philadelphia, PA Aseptic Manufacturing Technician BS in Biology, Biochemistry, Bioengineering, or Related Exp: 0-5 Years |
Iovance Biotherapeutics is seeking an Aseptic Manufacturing Technician to join the Operations team for the new Iovance manufacturing site. Responsibilities: Develop a comprehensive understanding of and be able to proficiently execute Iovance’s current cell therapy manufacturing process. Complete training sessions and ensure training documentation is maintained. Understands and complies with quality standards and requirements as documented. Provides operational support functions including materials stocking, kit preparation, reagent preparation, cleaning activities, and equipment maintenance. Supports technical transfer and additional research level testing activities. Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP). Completes recording of data to comply with regulatory requirements. | 5/15/2021 |
| 8762 | iRhythm Technologies San Francisco, CA RF Test Engineer - Product Development BS/MS in Electrical Engineering, Biomedical Engineering, or Related Exp: 0+ Years |
iRhythm is looking for a motivated, organized, and data driven, engineer with a history of developing test fixtures for medical device manufacturing. The role is part of the system team within product development. This individual will lead the development of our PCBA test fixtures for our next generation products. | 5/15/2021 |
| 8763 | Cambridge Isotope Laboratories Andover, MA Quality Control Analyst I BS/MS in Relevant Scientific Discipline Exp: 1+ Years |
Under the general supervision of a group leader, the QC Analyst I will perform various analytical techniques to determine isotopic enrichment, chemical purity, concentration and identity testing on a wide array of stable isotope-labeled materials (13C, 15N, Deuterium, and 18O isotopes). The role will focus primarily on NMR (1H, 2H, 31P, 19F, qNMR), GC, and wet chemistry analyses of solutions and neat materials, in support of the CIL production chemists, Operations & Logistics group and ISO 17025 reference materials program. | 5/15/2021 |
| 8764 | Cambridge Isotope Laboratories Andover, MA Operations & Logistics Technical Assistant BS in Chemistry or Related Exp: 0+ Years |
The O&L Technical Assistant provides technical support for various functions within the Operations and Logistics Department. This individual will aide in fulfilling the day-to-day O&L responsibilities associated with support of the Quality Review Group and the Documentation Team in a variety of functions, as well as other technical, detail-oriented assignments designated by department management. | 5/15/2021 |
| 8765 | Cambridge Isotope Laboratories Tewksbury, MA Quality Assurance Associate BS in Science or Quality Exp: 0-2 Years |
The incumbent be part of a GMP/ISO environment responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components. | 5/15/2021 |
| 8766 | Cambridge Isotope Laboratories Andover, MA Quality Control Technician BS in Relevant Scientific Discipline Exp: 1+ Years |
Responsibilities: Monitor, calibrate and maintain laboratory equipment as a routine. Sample and transport raw materials and product materials. Maintain general and chemical supplies in support of laboratory. Perform some basic analytical testing such as pH and conductivity analysis. Read, understand, and follow GMP guidelines and practices. | 5/15/2021 |
| 8767 | Cambridge Isotope Laboratories Andover, MA Associate Chemist BS in Chemistry or Related Exp: 0-2 Years |
Under the supervision of a group leader or supervisor, the Associate Chemist will work alongside an experienced scientist executing syntheses of isotopically labeled (13C, 15N, 18O and D isotopes) targets utilizing highly detailed SOPs and procedures. | 5/15/2021 |
| 8768 | Cambridge Isotope Laboratories Xenia, OH Quality Assurance Associate I BS in Chemistry or Related Exp: 0-2 Years |
Under general supervision, the primary responsibility of the GMP QA Associate I is to work as a team member to ensure and maintain the Company’s cGMP (Current Good Manufacturing Practices) compliance. | 5/15/2021 |
| 8769 | Cambridge Isotope Laboratories Xenia, OH Process Technician BS in Relevant Scientific Discipline Exp: 0+ Years |
CIL Process Technicians work in a team-based environment and are responsible for safety, production, maintenance, and product quality. Technicians are expected to understand and use automated control systems, production machinery, and laboratory equipment. Ability to work unsupervised and a willingness to succeed is required. | 5/15/2021 |
| 8770 | Jnana Therapeutics Boston, MA Senior Research Associate/Associate Scientist (Immunology) BS/MS in Immunology, Biology, or Related Exp: 0+ Years |
Responsibilities: Primary human immune cell isolation, culture, differentiation, and functional assays. De novo development of novel phenotypic and reporter assays. Measurement of cytokine production from multiple immune cell phenotypes (MSD/AlphaLISA). Assisting with molecular biology and cloning: Gibson assembly, bacterial transformation, and DNA mini-/midi-preps among others. | 5/15/2021 |
| 8771 | Jnana Therapeutics Boston, MA Biology Research Associate BS/MS in Biology or Related Exp: 0+ Years |
Jnana Therapeutics is seeking an enthusiastic and highly motivated Research Associate to support internal SLC drug discovery programs. Through small molecule screening and a range of cell-based assays, their research aims to expand their understanding of SLC transporter biology and ultimately discover drugs modulating these proteins. Prior experience is preferred but not required. Strong commitment and good work ethic are essential. Levels can be flexible based on experience. | 5/15/2021 |
| 8772 | Integer Minneapolis, MN Quality Engineer BS in Relevant Scientific/Engineering Discipline Exp: 0-3 Years |
The primary purpose of this job is to apply intensive and diversified knowledge of engineering principles and practices in broad areas of assignments and related fields. Ensures Integer internal and external customer expectations are met or exceeded. | 5/15/2021 |
| 8773 | Integer Chaska, MN Industrial Engineer I BS in Industrial Engineering or Related Exp: 0-3 Years |
The primary purpose of this job is to work with key business partners to drive value improvement guided by lean principles in order to support business strategy and priorities. Specifically, develop ways to increase productivity, maximize efficiency, and manage human capital more effectively. | 5/15/2021 |
| 8774 | JOINN Biologics San Francisco, CA Associate Scientist / Scientist — Process Development Upstream BS/MS in Chemical Engineering, Bioengineering, Biochemistry, Biotechnology, Biology, or Related Exp: 0-5 Years |
The incumbent will work with internal and external partners, to support bulk process development, characterization, technology transfer, and validation studies associated with the development and implementation of manufacturing processes, systems and facilities related to therapeutic mAbs and proteins. | 5/15/2021 |
| 8775 | JRF Global Audubon, PA Scientist I / Entry Level Chemist BS/MS in Chemistry or Related Exp: 1-3 Years |
Responsibilities: Set up experiments under the guidance of a Scientist II and/or Team Lead Operate equipment, observe and log the progress of experiments. Promptly submit experimental data / findings to the supervisor. Promptly inform the supervisor of any problems encountered during the experiments. Assist in data entry in various formats and verify accuracy of data entry. Assist in writing drafts of Protocols and Reports.Responsibilities: Set up experiments under the guidance of a Scientist II and/or Team Lead Operate equipment, observe and log the progress of experiments. Promptly submit experimental data / findings to the supervisor. Promptly inform the supervisor of any problems encountered during the experiments. Assist in data entry in various formats and verify accuracy of data entry. Assist in writing drafts of Protocols and Reports. | 5/15/2021 |
| 8776 | JRF Global Audubon, PA Quality Assurance Officer BS/MS in Chemistry or Related Exp: 1-3 Years |
Responsibilities: Position provides quality assurance (QA) functions for the US based regulatory chemistry program, requiring knowledge and experience with local, state, federal, and foreign government regulations (e.g., U.S. Federal Insecticide, Fungicide, Rodenticide Act, U.S. Good Laboratory Practices (GLP), European and Canadian OECD, and JMAFF study requirements). Assists in maintaining the QA database system for JRF America. Assists in scheduling and conducting inspections of JRF America studies and facilities to ensure that all studies and facilities are conducted in accordance with the appropriate GLP regulations. | 5/15/2021 |
| 8777 | JRF Global Audubon, PA Operations Coordinator BS in Relevant Scientific Discipline Exp: 0+ Years |
The Operations Coordinator will be involved in the management of services and processes that support the core business of the organization, ensuring the organization has the best working environment for its employees and their activities. The Operations Coordinator will continually work on improving the critical activities required for the efficient and effective functionality of the lab. | 5/15/2021 |
| 8778 | J-STAR Research South Plainfield, NJ Principal Engineer-Drug Substance MS in Chemistry or Biochemical Engineering Exp: 6+ Months |
Responsibilities: Perform multi-step drug substance synthesis and API crystallization in the range from milligrams to kilograms under cGMP and FDA compliance. Conduct compound impurities and chemical structure elucidation for chemical intermedia and drug substance utilizing techniques of FTIR, 1 H-NMR, LC/MS, UV-Vis, HPLC, and GC. Execute pharmaceutical unit operations simulation/modeling to support characterization and process challenges in development of API. Conduct pharmaceutical kinetic study to facilitate scale-up of controlled crystallization process in CSTR (Continuous Stirred Tank Reactor). | 5/15/2021 |
| 8779 | J-STAR Research South Plainfield, NJ Research Scientist MS in in Chemistry, Chemical Engineering or Related Exp: 1+ Years |
Responsibilities: Conduct solid-state screening and analyses of pharmaceutical samples in both GMP and non-GMP environments, utilizing a variety of analytical tools, including x-ray, thermal, spectroscopic, and wet chemistry analytical techniques. Support crystallization process development by conducting studies involving compound properties and experimental conditions. Conduct stability, performance, and evaluation studies in pre-formulation and formulation support. Participate in the development of enabling technology and experiments to facilitate the co-processing and development of API and drug products. | 5/15/2021 |
| 8780 | Jumpcode Genomics San Diego, CA Research Associate MS in Relevant Scientific/Engineering Discipline Exp: 1+ Years |
The Research Associate performs experiments in the laboratory and generates next generation sequencing (NGS) data to support the development of Jumpcode products. The Research Associate is responsible for the development of NGS-based genomics workflows, including, but not limited to, those for targeted, whole genome and whole transcriptome sequencing. This role runs and maintains sequencing instruments to generate next generation sequencing (NGS) data in support of Jumpcode product development. | 5/15/2021 |
| 8781 | Just Evotech Biologics Seattle, WA Associate Scientist, Antibody Discovery – Phage Display BS/MS in Life Sciences, Cellular/Molecular Biology, or Related Exp: 1-5 Years |
This position will be part of a cross-disciplinary team developing antibody libraries for discovery, therapeutic optimization, and high throughput characterization. The successful candidate will support the invention, design, and implementation of phage display library methods to drive biotherapeutic development. A strong foundation in molecular biology and vector cloning is required for this position, with additional experience in phage display and/or bacterial protein expression strongly desired. This individual must also possess strong communication and collaboration skills, a desire to learn new scientific concepts and domains, and an ability to work directly with scientific staff across multiple disciplines. | 5/15/2021 |
| 8782 | Just Evotech Biologics Seattle, WA Associate Scientist, Antibody Discovery Bioassay BS/MS in Life Sciences, Cellular/Molecular Biology, or Related Exp: 0-5 Years |
Just is seeking a highly motivated and creative Associate Scientist that desires a significant opportunity to help invent the technologies required to improve worldwide access to biotherapeutics. This position will be part of a cross-disciplinary team discovering therapeutic antibodies from display libraries and optimization campaigns. The successful candidate will support the invention, design, and implementation of cell-based, functional bioassay and immunoassay methods to drive biotherapeutic development. A strong foundation in assay development, cell biology and molecular biology is required for this position, with additional experience in antibody discovery, target validation, in vivo PK models and automation preferred. This individual must also possess strong communication and collaboration skills, a desire to learn new scientific concepts and domains, and an ability to work directly with scientific staff across multiple disciplines. | 5/15/2021 |
| 8783 | Just Evotech Biologics Seattle, WA Associate Scientist, Bioreactor Process Design BS in Engineering, Biochemistry, or Related Exp: 0-5 Years |
Just is seeking a motivated and hardworking team member who desires a significant opportunity to improve worldwide access to biotherapeutics. This person will join a fast-paced, collaborative, and multidisciplinary team to support bioreactor process development at 1-50L scale for the advancement of low-cost biotherapeutics manufacturing. The successful candidate will be detail-oriented, self-motivated, and efficient in completing tasks. Experience with equipment cleaning and maintenance, ordering and managing inventory, and organizing workspace and tasks are preferred. Strong written and verbal communication skills, and experience with typical software packages (such as Microsoft Office, Google Suite, etc) are desired. The ideal candidate is curious, creative, engaged, works well independently and in teams, and constantly looks for ways to improve processes and technology. | 5/15/2021 |
| 8784 | Just Evotech Biologics Seattle, WA Associate Scientist, Drug Product Design BS in Biochemistry, Chemistry, Biophysics,Chemical Engineering, or Related Exp: 0-3 Years |
Just-Evotec Biologics is seeking an energetic, team-oriented researcher for a hands-on, laboratory based role supporting all stages of drug product development from early stage molecular design to formulation verification and commercial stage formulation design of protein therapeutics. The successful candidate will have experience working in an analytical laboratory setting and familiarity with biophysical, chromatographic, electrophoretic, and spectroscopic techniques. The candidate must possess a strong ability to work as a team member while supporting multiple projects. Strong organizational, written, and verbal communication skills are necessary. The ideal candidate is efficient, curious, creative, enthusiastic, works well independently and in teams, and looks for ways to improve processes and technology. | 5/15/2021 |
| 8785 | Just Evotech Biologics Redmond, WA Associate Scientist, Functional Biocharacterization BS in Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering, Chemistry or Related Exp: 0-5 Years |
Just is seeking a motivated and creative Associate Scientist who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work with a multidisciplinary team for the analytical and functional biocharacterization of large molecule therapeutics and analysis of process impurities. Experience with ELISA binding assays, DNA extraction, and PCR preferred. Additional experience with cell-based and ligand-receptor binding assays, as well as high-throughput methods and liquid handling robotics beneficial. The successful candidate has strong written and verbal communication skills and is interested in ways to improve technology. The ability to multitask and to work both independently and in teams in a fast-paced collaborative environment is necessary. | 5/15/2021 |
| 8786 | Just Evotech Biologics Redmond, WA Associate Scientist, High Throughput Analytical BS in Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering, Chemistry or Related Exp: 0-5 Years |
Just is seeking a motivated and creative Associate Scientist, who desires a significant opportunity to improve worldwide access to biotherapeutics. We are looking for a motivated scientist to join a fast-paced, collaborative, and multidisciplinary team. As a member of the High Throughput Analytical group, you will support process development through application of H/UPLC and CE methodologies. Additional experience with other analytical techniques as well liquid handling robotics is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. | 5/15/2021 |
| 8787 | Just Evotech Biologics Redmond, WA Associate Scientist, Protein Expression BS in Relevant Scientific Discipline Exp: 0-5 Years |
Just is seeking a motivated and creative researcher who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work as a member of a small but highly experienced and innovative team to develop cell lines for the purpose of manufacturing biologic therapeutics. The successful candidate will have experience with cell culture as well as a strong foundation in cell and molecular biology. Experience in cell line development, cell culture automation, and expression vector design, is a plus. The candidate must possess strong written and verbal communication skills, strong organizational skills, a desire to learn new scientific concepts, and an ability to work directly with scientific staff across multiple disciplines. | 5/15/2021 |
| 8788 | Kallyope New York, NY Chemistry Research Associate BS in Chemistry Exp: 0+ Years |
Kallyope is seeking a self-motivated chemist to work as a member of an integrated team focused on the discovery of new drug targets leading to transformational therapeutics. The successful applicant will assume primary responsibility for maintaining Kallyope’s internal compound collection and coordinating compound logistics. They will also contribute to drug discovery and formulation efforts through synthesis and basic physicochemical characterization of compounds. This represents a unique opportunity to impact multiple therapeutic programs driven by Kallyope’s cutting-edge biology on the gut and gut-brain axis. | 5/15/2021 |
| 8789 | Kallyope New York, NY Chemistry Senior Research Associate BS in Organic Chemistry, Medicinal Chemistry or Related Exp: 0+ Years |
Kallyope is seeking a highly creative, self-motivated medicinal chemist with experience in drug discovery to work as a member of an integrated team developing a novel platform for the discovery of new drug targets leading to transformational therapeutics. The successful applicant will contribute to the drug discovery process from target identification through candidate nomination and will have the unique opportunity to impact multiple therapeutic programs driven by Kallyope’s cutting-edge biology on the gut and gut-brain axis. They will also assume responsibility for maintaining Kallyope’s internal compound collection and will contribute to formulation efforts through basic physicochemical characterization of compounds. | 5/15/2021 |
| 8790 | Kallyope New York, NY Biomarker Research Associate BS/MS in Biology, Chemistry, or Related Exp: 0+ Years |
The Biomarker Research Associate will be a member of a team charged with establishing a suite of biomarker assays to asses target engagement of investigational drugs in early clinical development. Candidates must be highly motivated with previous experience working in a regulated environment following established SOP’s. Successful candidates must be able to work effectively both in a collaborative setting and independently while possessing outstanding written, visual, and oral communications skills. | 5/15/2021 |
| 8791 | Kallyope New York, NY Cell Biology Research Associate MS in Relevant Scientific Discipline Exp: 0+ Years |
The Cell Biology Research Associate will be a member of the newly established Immunology and Inflammation team responsible for supporting mechanism of action type studies from a pharmacological perspective. This position will be responsible for establishing reliable read outs of cellular function and biological pathway activity in both in vitro and in vivo/ex vivo samples. Candidates should be highly motivated and comfortable with multiple types of assays and read outs with extensive hands-on experience in cell biology research. Successful candidates must be able to work effectively both in a collaborative setting and independently while possessing outstanding written, visual and oral communications skills. | 5/15/2021 |
| 8792 | Kallyope New York, NY In Vitro Pharmacology Research Associate BS in Biology or Related Exp: 0+ Years |
The In Vitro Pharmacology Research Associate will be a key member of the team charged with cell line development and maintenance for in vitro assays. Candidates must have a biology background and an extensive experience in tissue culture techniques. This role will be responsible for the majority the tissue culture work of the group. Experience with molecular biology, GPCR signaling and in in vitro pharmacology is a plus. Successful candidates must be able to work effectively both in a collaborative setting and independently and possess outstanding written, visual and oral communications skills. | 5/15/2021 |
| 8793 | Kallyope New York, NY Pharmacology In Vivo Research Associate BS in Biology or Related Exp: 0+ Years |
The In Vivo Pharmacology Research Associate will be a key member of the team charged with developing, qualifying, and executing in vivo assays. Candidates must have outstanding experience in multiple aspects of in vivo pharmacology including formulation, dosing, pharmacokinetic sampling and necropsy. Successful candidates must be able to work effectively both in a collaborative setting and independently and possess outstanding written, visual and oral communications skills. | 5/15/2021 |
| 8794 | imarc Strongsville , OH Clinical Support Services Associate BS in Science, Engineering, or Health Related Field Exp: 0+ Years |
This is a highly responsible and professional position. The CSSA I will work with a Sponsoring company or CRO in supporting device, biologics, or pharmaceutical studies with an emphasis placed on ensuring the highest ethical and clinical standards. The general focus of this position is in organizing and administering supporting clinical services: Safety Management [Data Safety Monitoring Board (DSMB) / Clinical Events Committee (CEC)], Client Training, Consulting, Site Support, and Internal IMARC Training. | 5/7/2021 |
| 8795 | imarc Strongsville , OH Internal Clinical Research Associate I BS in Science, Engineering, or Health Related Field Exp: 0+ Years |
The Internal Clinical Research Associate I (ICRA I) will provide support to the various clinical departments within IMARC. Responsibilities: Obtain a familiarity with and understanding of clinical trial documentation format, content requirements, and operational procedures. Update internal databases to ensure sponsor and study-specific timelines are met. Support clinical staff in all departments. Perform document review for quality control of study documents, including maintenance of internal files, report corrections, document filing and processing. This includes peer-reviewing confirmation letters, formatting training presentations, and assisting with other review as requested. | 5/7/2021 |
| 8796 | Immunetrics Pittsburgh, PA Mathematical Modeler - Quantitative Systems Pharmacology MS in Chemical Engineering, Electrical Engineering, Mathematics, Physics, or Related Exp: 0+ Years |
A QSP Mathematical Modeler working for Immunetrics will be part of a multidisciplinary team of professionals who design and develop mechanistic computational models of complex biological systems to support their clients’ needs. As a member of this team, the modeler will work with both internal and client biologists to utilize research literature to understand biological pathways and physiological processes. The modeler’s responsibilities will span the entire modeling life cycle: analysis, specification, design, implementation, parameter estimation, model training, testing, debugging, population generation, verification, validation, documentation, and maintenance. | 5/7/2021 |
| 8797 | IMMY Norman, OK Regulatory Affairs Specialist BS in Relevant Scientific Discipline Exp: 0+ Years |
The Regulatory Affairs Specialist is primarily responsible for preparing IVD regulatory documents for submission to various regulatory agencies, both domestic and international | 5/7/2021 |
| 8798 | Impact Analytical Midland, MI Analytical Technologist I/II BS in Relevant Scientific Discipline Exp: 0+ Years |
Under direct supervision, the Analytical Technologist is responsible for laboratory work in collaboration with others. The Analytical Technologist can perform routing tasks in sample handling and logging, preparing glassware, laboratory maintenance and sample preparation. | 5/7/2021 |
| 8799 | Impact Analytical Midland, MI Quality Reviewer BS in Chemistry, Biochemistry, or Related Exp: 0+ Years |
In collaboration with the current quality team members, the successful candidate would be trained to support quality control and quality assurance functions. These functions may include technical report review at project completion and internal auditing against both ISO 9001 and/or 17025 quality standards, as well as GLP/cGMP regulations. | 5/7/2021 |
| 8800 | Incyte Wilmington, DE Research Scientist, In Vitro Pharmacology BS/MS in Cancer Biology, Pharmacology or Related Exp: 0+ Years |
The candidate will be responsible for performing in vitro studies for cancer drug discovery programs. This includes the development of relevant preclinical model systems for the identification and validation of novel therapeutic targets. The successful candidate is able to work with minimal supervision in most molecular and cellular biology techniques and demonstrates an understanding of cancer biology. Experience with oncogenic signaling pathways and targeted therapies is an advantage. The candidate is expected to work with their supervisor to design and execute a research plan that will answer critical questions about compounds and targets under evaluation. | 5/7/2021 |
| 8801 | Incyte Wilmington, DE Research Scientist, Antibody Pharmacology BS/ MS in Immunology, Cancer Biology, Pharmacology or Related Exp: 0+ Years |
the candidate will be responsible for performing in vitro and in vivo studies for cancer immunotherapy drug discovery programs. | 5/7/2021 |
| 8802 | Incyte Wilmington, DE Sr. Research Scientist, Antibody Pharmacology MS in Immunology, Cancer Biology, Pharmacology or Related Exp: 0+ Years |
The candidate will be responsible for performing in vitro and in vivo studies for cancer immunotherapy drug discovery programs. This includes the development of relevant model systems for the identification and validation of novel therapeutic targets. The successful candidate is able to work independently and demonstrates a broad understanding of immunology and cancer biology, being able to use this knowledge to design and execute a research plan that answers critical questions about compounds and targets under evaluation. | 5/7/2021 |
| 8803 | Inivata Research Triangle Park, NC Molecular Technologist BS/MS in Medical Technology, Clinical Laboratory Science, Chemical, Physical, or Biological Science, or Related Exp: 1-3 Years |
The role of Molecular Technologist is to perform DNA processing and sequencing analysis and review results from high-complexity molecular testing of human (patient) specimens under CLIA/CAP and other regulatory guidelines. They perform patient testing utilizing the molecular workflows associated with the relevant clinical diagnostic assays | 5/7/2021 |
| 8804 | Inivata Research Triangle Park, NC Specimen Processor AS/BS in Relevant Scientific Discipline Exp: 0-2 Years |
The role of Specimen Processor I, II, III, Lead is to accurately accession incoming specimens into the Laboratory Information System. This includes receiving and opening packages, accessioning requisition information into laboratory LIS, application of barcodes to sample tubes and ensuring samples are ready for processing in the laboratory. The Specimen Processor is also responsible for initial processing of blood samples to plasma for DNA extraction. | 5/7/2021 |
| 8805 | Inova San Diego, CA Chemist I - IFA Slides BS in Biological, Chemical, or Related Sciences Exp: 0-1 Years |
Assists with preparation of autoimmune diagnostic Immunofluorescence Assay (IFA) cell culture slide products according to established procedures. Major duties include mammalian cell culture, immunofluorescence cell suspension and slide preparation activities. | 5/7/2021 |
| 8806 | Inova San Diego, CA Research Associate I BS in Biological, Chemical, or Related Sciences Exp: 1-2 Years |
This position assists in the development of current and future Inova Diagnostic product lines by performing laboratory activities to assist in the development of new assays and/or the identification of potential new biomarkers. This position works under the supervision of the R&D management team and performs lab activities of limited scope, following good laboratory documentation practices and in accordance with Standard Operating Procedures and other Research and Quality System requirements. | 5/7/2021 |
| 8807 | Inova San Diego, CA Chemist I - Elisa Controls BS in Biological or Related Science Exp: 0-2 Years |
Performs major manufacturing duties including assistance with the activities required to produce ELISA calibrators, controls and conjugates. | 5/7/2021 |
| 8808 | Inovio San Diego, CA Assistant, Quality Assurance BS in Relevant Scientific Discipline Exp: 1+ Years |
The Quality Assurance (QA) Assistant has the primary responsibility for supporting QA activities along with supporting Quality Systems and compliance as needed. The QA Associate performs a wide variety of duties, including supporting the daily QA Bioanalytics (laboratory) departmental operations, aiding with equipment program management and oversight of information migration to Blue Mountain Regulatory Asset Manager (RAM). This process is subdivided into two steps: 1) set up of equipment (asset) database asset information upload at the first San Diego facility (until scope of work is complete); and 2) transition to completion of asset information upload at the second San Diego facility. | 5/7/2021 |
| 8809 | Inovio San Diego, CA Research Associate I BS in Immunology, Cell or Molecular Biology, or Bioengineering. Exp: 0-1 Years |
The RAI works under general and specific direction in performing a spectrum of techniques in both cell culture and immunology. The RAI works collaboratively and independently in the lab, solves problems, completes required documentation, and performs general lab duties. | 5/7/2021 |
| 8810 | Inovio San Diego, CA Research Associate II (Sample Management & Analytical Immunology) MS in Immunology, Cell Biology, Analytical Biochemistry, or Related Exp: 0+ Years |
The Research Associate II (RA) is a member of the Analytical Sciences group primarily responsible for coordinating and executing the clinical sample management life cycle and activities supporting drug discovery and clinical development. Working closely with clinical and laboratory project leads and other laboratory staff, the RA is responsible for maintaining the clinical laboratory sample life cycle management, which includes receiving human clinical blood samples, processing or coordinating with other lab personnel on the processing schedule. performing sample reconciliation per project and clinical study protocols. | 5/7/2021 |
| 8811 | Inscopix Palo Alto, CA Neuroscience Technical Project Manager MS in Neuroscience Exp: 0+ Years |
Inscopix is seeking a Neuroscience Technical Project Manager to lead their product development cycle from managing requirements to leading the validation process and launch. The candidate will collaborate with an interdisciplinary team of neuroscientists, data scientists and engineers from software, mechanical, optical and electrical engineering fields. | 5/7/2021 |
| 8812 | Inscripta Boulder, CO Technical Informatics Specialist BS in Computational Biology, Computer Science, Molecular Biology, Genomics, Biochemistry, or Related Exp: 0+ Years |
The TIS will leverage their experience in bioinformatics and genomics workflows to provide premier support for the InscriptaResolver analysis software. They will help customers to analyze sequencing data from cell libraries generated by our platform, determine library genotypic composition, identify edits and correlate/interpret genotypic and phenotypic assay data. | 5/7/2021 |
| 8813 | Inscripta Boulder, CO Research Associate/Sr. Research Associate BS/MS in Genetics, Microbiology, Molecular Biology, or Related Exp: 0+ Years |
As a member of the Applications Development team, the Research Associate/Sr. Research Associate will be an internal customer of Inscripta’s Onyx platform, applying their digital genome engineering capabilities to tackle cutting edge research in E. coli and other microbes. Inscripta is seeking a diverse candidate to work in a collaborative group to apply principles of forward engineering and genome discovery across a variety of microbial strains. The Research Associate/Sr. Research Associate will work closely with internal and external collaborators on cross-functional teams to generate high-quality data across multiple projects. | 5/7/2021 |
| 8814 | Integral Molecular Philadelphia, PA Project Manager - Antibody iscovery MS in Cell Biology, Molecular Biology, Drug Discovery, or Related Exp: 1-2 Years |
Integral Molecular is seeking a highly organized BS/MS level scientist to manage projects utilizing their antibody discovery platform (Membrane Protein Solutions). | 5/7/2021 |
| 8815 | Integral Molecular Philadelphia, PA Research Associate BS in Biology, Bioengineering, or Related Exp: 1-2 Years |
Integral Molecular is seeking a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. | 5/7/2021 |
| 8816 | Integral Molecular Philadelphia, PA Research Technician BS in Biology, Chemistry, Medical Technology, or Related Exp: 6 Months-2 Years |
Integral Molecular is seeking an entry level Laboratory Technician to perform vital laboratory tasks to support the continued success of their research teams. The candidate will be part of a lab management team that works in a unified and collaborative manner to ensure the efficient operation of the laboratory. | 5/7/2021 |
| 8817 | Integral Molecular Philadelphia, PA Biotechnology Sales Associate BS in Life Sciences, Biology, or Chemistry Exp: 1+ Years |
Responsibilities: Be a key part of the sales, marketing, and business development team of a biotech company. Work with senior management in the planning, strategy, and execution of product development. Conduct marketing and sales efforts targeting large and small antibody biotech customers. | 5/7/2021 |
| 8818 | Intellia Therapeutics Cambridge, MA Associate Scientist, Immunology MS in Immunology, Cell Biology, or Related Exp: 0+ Years |
As an Immunologist, you will join the Intellia ex-vivo group, where they leverage top-notch CRISPR technology to fully unleash the power of cell-based therapy for autoimmune and Immuno-Oncology indications. | 5/7/2021 |
| 8819 | Intellia Therapeutics Cambridge, MA Associate Scientist, Pre-clinical Next Generation Sequencing BS/MS in Molecular Biology or Related Exp: 0+ Years |
As an Associate Scientist, you will help support the characterization and quantitation of gene editing events using high throughput next generation sequencing (NGS). | 5/7/2021 |
| 8820 | Intellia Therapeutics Cambridge, MA Automation Engineer BS/MS in Molecular Biology or Engineering Exp: 0+ Years |
As an Automation Engineer, for a genome editing company, a major focus is on NGS library prep methods to identify gene editing events in support of the company’s pipeline by utilizing our collection of liquid handling and automated high-throughput plate processing platforms. Your primary responsibility will be to collaborate with a team of engineers and scientists to automate assays and assist with improving overall lab productivity. | 5/7/2021 |
| 8821 | Intellia Therapeutics Cambridge, MA Senior Research Associate, Cell Therapy BS/MS in Immunology, Cell Biology, or Related Exp: 0-2 Years |
Intellia is seeking a highly skilled and motivated Senior Research Associate for their ex-vivo Cell Therapy group. The primary responsibility for this position is developing and optimizing in vitro immunological assays to evaluate engineered immune cell function for cancer therapy. | 5/7/2021 |
| 8822 | Intellia Therapeutics Cambridge, MA Manufacturing Associate, Nucleic Acid Therapeutics Development & Manufacturing BS in Chemistry, Biochemistry, or Related Exp: 1+ Years |
The Internal Manufacturing team is a small team of 5 that is responsible for cGMP upstream and downstream manufacturing of mRNA and LNP to support early phase clinical trials. They also perform continuous process improvement including developing and execute process optimization studies. You will report to the Senior Manager, Internal Manufacturing. | 5/7/2021 |
| 8823 | Intellia Therapeutics Cambridge, MA Nonclinical Operations Lead BS/MS in a STEM Field Exp: 1-2 Years |
The successful candidate will have opportunities to work with principal investigators to manage complex nonclinical activities while gaining broad experience in product development in an industry environment. | 5/7/2021 |
| 8824 | Intellia Therapeutics Cambridge, MA Senior Research Associate, Bioanalytical Assay Development MS in Biology, Chemistry, Biochemistry, or Related Exp: 0+ Years |
In this role, you will have an opportunity to collaborate cross-functionally to perform data analysis, review, and communicate findings to both internal and external partners. | 5/7/2021 |
| 8825 | Intersect Menlo Park, CA Microbiology I BS in Microbiology Exp: 1-2 Years |
You will: Support and execute activities and goals associated with microbiology, environmental monitoring, sterilization, and bioburden testing programs for new product development and commercial manufacturing. Support cross functional teams with respect to microbiology related matters. | 5/7/2021 |
| 8826 | Intuitive Norcross, GA Surgical Annotation Specialist BS in Biological or Related Science Exp: 1-3 Years |
Primary Function of Position: Contribute broadly to the Advanced Product Development team, responsible for advanced analytics and new technology development focused on the performance for next generation robotic surgery platforms. | 5/7/2021 |
| 8827 | Intuitive Sunnyvale, CA Clinical Evaluation Specialist III MS in Scientific Discipline Exp: 0-2 Years |
This position reports to Manager, Clinical Affairs, (Clinical Evaluation) and requires a strong candidate with experience in medical writing of clinical regulatory documents. The position will mainly focus on development of Clinical Evaluation Reports (CERs), with potential for future additional responsibility for development of other clinical evidence documents. The purpose of this job is to author and develop clinical evaluation reports (CERs) per MEDDEV 2.7.1 Rev 4, to meet essential requirements in support of submission for CE Mark application to obtain Declaration of Conformity and EU market clearance, recertification and proposed indication/labeling changes, as well as CER updates to maintain EU product conformance. | 5/7/2021 |
| 8828 | Intuitive Sunnyvale, CA Staff Mechanical Engineer MS in Physics, Mechanical Engineering, Materials Science or Related Engineering or Scientific Discipline Exp: 0+ Years |
Responsibilities: Work in a small cross-functional project team to design, develop and verify designs for flexible surgical instruments and accessories. Work with KOLS and develop concepts based on early clinical, marketing, and customer inputs including early prototyping of designs. Lead early stage ideation and prototyping efforts. Evaluations of prototypes, critically analyze results, and make design changes or recommendations with the design team. Provide support for pre-clinical and clinical labs | 5/7/2021 |
| 8829 | Invenra Madison, WI Scientist/Senior Scientist - Antibody Engineering MS in Molecular Biology, Cell Biology, Immunology, or Related Exp: 0-3 Years |
This individual will contribute towards the direction of Invenra's antibody screening technology from candidate identification through validation. The candidate will work with other scientists within the team to design and execute experiments, analyze data and communicate results in an inter-disciplinary environment. The position requires excellent scientific and problem-solving skills, with a strong focus on creative solutions to technical problems. | 5/7/2021 |
| 8830 | Invenra Madison, WI Scientist/Senior Scientist - Protein Biophysics and Innovation MS in Biochemistry, Biophysics, Molecular Biology, Cell Biology, Immunology, or Related Exp: 1+ Years |
This individual will focus on developing cutting-edge BLI and LSA workflows to expand and revolutionize Invenra’s current drug discovery pipeline. As part of the Innovation group, the successful applicant will work in a team to improve the efficiency or quality of immune-oncology drug discovery. Details of the job include managing and developing protocols on BLI and LSA instruments, protein binding experiments, high-throughput drug screening, and optimizing project-specific screening funnels. The position requires excellent understanding of protein biochemistry, scientific and problem-solving skills, detailed and well-organized, technological savvy, and the ability to try new things. | 5/7/2021 |
| 8831 | Invenra Madison, WI Associate Scientist/Scientist - Translational Bioprocess BS/MS in Biochemistry or Related Exp: 0+ Years |
Invenra is seeking a highly motivated Associate Scientist / Scientist to join their Translational BioProcess team to support downstream protein purification and process development activities. This individual will support the Invenra antibody discovery platform by helping to transition candidate multi-specific antibodies to drug leads. The successful candidate will use their knowledge of protein biochemistry to work with the translational BioProcess group to produce materials needed for in vivo or cell culture experiments, develop scalable and robust purification processes for individual lead candidates, perform the experimental work, and maintain the documentation needed to successfully transfer purification processes to a Contract Manufacturing Organization in preparation for IND submissions. | 5/7/2021 |
| 8832 | Invitae Boulder, CO Technical Support Specialist I BS in Biology, Molecular Biology, Genetics, Biochemistry, or Related Exp: 0+ Years |
The Technical Support Specialist provides first level technical support on Invitae Somatic Oncology products from the Invitae office in Boulder, CO. This individual will escalate customer inquires effectively, collect customer feedback and share this with internal teams to improve products. This individual will assist in coordinating activities for special programs as needed. | 5/7/2021 |
| 8833 | Invitae San Francisco, CA Clinical Bioinformatics Analyst - Medical Affairs MS in Computational Biology, Statistical Genetics, Population Genetics, Biostatistics, Bioinformatics, or Related Exp: 0+ Years |
This position is responsible for compiling and analyzing data for internal and external customers. The analyst would collect data and perform data analysis for scientific publications, marketing materials, external collaborations, and internal studies. Responsibilities include both simple data pulls as well as complex analyses that require original thinking and novel analysis. The candidate must be able to collaborate with customers at all levels of clinical and technical expertise, including genomic scientists, genetic counselors, medical geneticists, bioinformaticians, AI engineers, data scientists and computational biologists. In | 5/7/2021 |
| 8834 | Exact Sciences Madison, WI Laboratory Service Engineer I Bachelor?s degree in Engineering, Technology, Molecular Biology, Electronics, or related field. Exp: 1+ years |
The Laboratory Service Engineer I (LSE I) is responsible for the service and support of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. | 4/26/2021 |
| 8835 | Exact Sciences Redwood City, CA Laboratory Service Engineer I Bachelor?s degree in Engineering, Technology, Molecular Biology, Electronics, or related field. Exp: 1+ years |
The Laboratory Service Engineer I (LSE I) is responsible for the service and support of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. | 4/26/2021 |
| 8836 | Exact Sciences Baltimore, MD Quality Control Associate II Bachelor's degree in Chemistry, Molecular Biology or a science related field. Exp: 1+ years |
The Quality Control Associate II will participate and may take leadership in a variety of Quality Control functions, including but not limited to, raw material, in-process material, finished goods and stability testing; process and method development, characterization and validation, and quality documentation generation. | 4/26/2021 |
| 8837 | Exact Sciences Madison, WI Research & Development Laboratory Technician II Bachelor?s degree in biotechnology or related field. Exp: 1 year |
The R&D Laboratory Technician II will provide world class service and support for common R&D laboratory functions. The position is expected to follow detailed instructions and established procedures with minimal supervision. Duties include lab organization, equipment maintenance, cold storage sample management and miscellaneous tasks to help the labs run efficiently. | 04/26/2021 |
| 8838 | Exact Sciences Phoenix, AZ Bioinformatics Scientist I Master?s degree or PhD in Statistics, Data Mining, Mathematics, Engineering, or similar field of study. Exp: 1+ years |
The Bioinformatics Scientist I is a creative person who will conduct the development of data mining algorithms and tools using proprietary data and databases for scientific research and cancer biomarker discovery. The position offers exciting opportunity and significant growth potential within an innovative and dynamic genomic diagnostics company. | 04/26/2021 |
| 8839 | Fluke Biomedical Keene, NH Process Engineer I Minimum two-year engineering degree. Exp: 0 |
As a Janos Process Engineer on our team, you will learn firsthand how infrared optics and assemblies are manufactured and tested. Our products end up in equipment around the world supporting the US military and in commercial night vision products. | 04/26/2021 |
| 8840 | Foundation Medicine Morrisville, NC Molecular Technologist I (Sunday - Thursday 8:00am - 4:30pm Bachelor?s Degree in a chemical, physical, biological, or life science (per NYSDOH regulatory requirements). Exp: 1+ years |
The Molecular Technologist I performs procedures in a complex patient sample testing process with limited supervision. Most prominently, the position is responsible for solution and reagent preparation, equipment maintenance, and the handling and testing of patient specimens. The incumbent works one of three established shifts and may be assigned to work any day that the lab is operational. | 04/26/2021 |
| 8841 | Foundation Medicine Cambridge, MA Molecular Technologist I (Tues-Sat 3rd Shift) Bachelor?s Degree in a chemical, physical, biological, or life science (per NYSDOH regulatory requirements). Exp: 1+ years |
The Molecular Technologist I performs procedures in a complex patient sample testing process with limited supervision. Most prominently, the position is responsible for solution and reagent preparation, equipment maintenance, and the handling and testing of patient specimens. The incumbent works one of three established shifts and may be assigned to work any day that the lab is operational. | 04/26/2021 |
| 8842 | Foundation Medicine Cambridge, MA Molecular Technologist I (Tues-Sat 1st Shift) Bachelor?s Degree in a chemical, physical, biological, or life science (per NYSDOH regulatory requirements). Exp: 1+ years |
The Molecular Technologist I performs procedures in a complex patient sample testing process with limited supervision. Most prominently, the position is responsible for solution and reagent preparation, equipment maintenance, and the handling and testing of patient specimens. The incumbent works one of three established shifts and may be assigned to work any day that the lab is operational. | 04/26/2021 |
| 8843 | Foundation Medicine Cambridge, MA Molecular Technologist I (Tues-Sat 3rd Shift) Bachelor?s Degree in a chemical, physical, biological, or life science (per NYSDOH regulatory requirements). Exp: 1+ years |
The Molecular Technologist I performs procedures in a complex patient sample testing process with limited supervision. Most prominently, the position is responsible for solution and reagent preparation, equipment maintenance, and the handling and testing of patient specimens. The incumbent works one of three established shifts and may be assigned to work any day that the lab is operational. | 04/26/2021 |
| 8844 | Foundation Medicine Cambridge, MA Molecular Technologist I (Tues-Sat 3rd Shift) Bachelor?s Degree in a chemical, physical, biological, or life science (per NYSDOH regulatory requirements). Exp: 1+ years |
The Molecular Technologist I performs procedures in a complex patient sample testing process with limited supervision. Most prominently, the position is responsible for solution and reagent preparation, equipment maintenance, and the handling and testing of patient specimens. The incumbent works one of three established shifts and may be assigned to work any day that the lab is operational. | 04/26/2021 |
| 8845 | Organogenesis Canton, MA Process Development Associate I Requires B.S. in a scientific discipline. Exp: 0-5 years |
The Process Development Associate I is responsible for performing research and development experiments in support for projects and products. | 04/27/2021 |
| 8846 | Leidos San Antonio, TX Research Associate I Bachelor's degree. Exp: 1+ years |
The Defense Health Operation of Leidos is currently looking for a Research Associate to support biomedical research at the Naval Medical Research Unit, San Antonio (NAMRU-SA) in San Antonio, TX. | 04/30/2021 |
| 8847 | Leidos Annapolis Junction, MD Systems Engineer (Entry Level) A Bachelor?s degree in a Qualified Engineering Field or a related discipline. Exp: one (1) year |
The Systems Engineer applies systems engineering principles throughout the systems life cycle phases: Concept, Development, Production, Utilization, Support, and Retirement. | 04/30/2021 |
| 8848 | Leidos Groton, CT Test Engineer Bachelor's degree in engineering, computer science, physics, or mathematics. Exp: 0-2 years |
Leidos Military & Veterans Health Solutions Group is seeking a Test Engineer to support our operations at the Naval Submarine Medical Research Laboratory (NSMRL) in Groton, CT. | 04/30/2021 |
| 8849 | Eli Lilly Indianapolis, IN Chemist - QC - FTE Bachelor (4 yr College) degree in a science field related to the lab in which they are placed (e.g. chemistry, biochemistry). Exp: entry level position |
The chemist performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. The chemist completes second person verification of others results. | 04/30/2021 |
| 8850 | Eli Lilly Indianapolis, IN Quality Control - Chemistry Equipment Custodian/CSV Bachelor degree in scientific field related to the lab (Chemistry). Exp: 1-5 years |
To provide equipment lifecycle management support to the Parenteral QC Laboratories. Main support functions include specifying and purchasing equipment; authoring EQ packages, managing the EQ process, and providing daily operational support of laboratory equipment by ensuring the equipment is maintained in a qualified state of compliance. | 04/30/2021 |
| 8851 | Eli Lilly Indianapolis, IN Chemist ? QC ? IAPI- FDE Bachelor degree in a science related field. Exp: entry level position |
The Chemist � QC � IAPI performs accurate and timely testing of routine lab samples in accordance with appropriate GMP and safety guidelines. The Chemist � QC - IAPI also participates in second person verification (SPV) of analytical data, laboratory investigations, equipment calibrations and maintenance by executing well-defined protocols and procedures. | 04/30/2021 |
| 8852 | Eli Lilly Indianapolis, IN IAPI QC Chemist-FDE Bachelor degree in a science related field. Exp: entry level position |
The Chemist � QC � IAPI performs accurate and timely testing of routine lab samples in accordance with appropriate GMP and safety guidelines. The Chemist � QC - IAPI also participates in second person verification (SPV) of analytical data, laboratory investigations, equipment calibrations and maintenance by executing well-defined protocols and procedures. | 04/30/2021 |
| 8853 | Organogenesis Canton, MA Quality Control Analyst I/II, Inspector Graduate in the field of Biomedical Engineering or Biological Sciences. Exp: 1-5 years |
The QC Analyst I/II is responsible for performing final product release testing and final product visual inspection at the Canton, MA facility. The successful candidate will work closely with Sr. Level QC Engineers / Scientists / Analysts on ongoing projects in support of general quality activities and initiatives, product / process development, analytical support, pre-validation, and validation activities, amongst other general duties routinely performed in the Quality Control. | 04/30/2021 |
| 8854 | Meridian Medical Technologies Boulder, CO Associate Scientist, Structural Biology BS in Cell Biology, Molecular Biology, Biochemistry or related biological science. Exp: 1 year |
The Structural Biology group within Pfizer-Boulder R & D has a position for a junior level scientist with cell culture experience. This scientist will be responsible for maintaining and scaling up (ﾳ5L) insect cell, mammalian cell, and sometimes E. coli cultures for recombinant protein expressions. | 04/30/2021 |
| 8855 | Meridian Medical Technologies Pearl River, NY Associate Scientist (Cell-culture) BS/BA or MS/MA degree in life science (e.g. biology, cell biology, immunology, virology, microbiology). Exp: 0-2 years |
The responsibilities of this position include but are not limited to preparing, qualifying and maintaining/ordering inventory of various reagents for cell culture, and assay work, monitoring the performance of the various cell lines, recording data into our Laboratory Information Management System (LIMS), growing, expanding and supplying different types of adherent or suspension cell lines as needed for assay development and regulated testing and helping to improve cell production processes to accommodate the increasing demand for cells. | 04/30/2021 |
| 8856 | Meridian Medical Technologies Pearl River, NY Associate Scientist, Ligand Binding Immunoassays Bachelor?s or master?s degree in biology, microbiology, molecular biology, chemistry, or relevant field of science. Exp: 0-3 years |
You will have the important role to generate high-quality immunoassay data within the Ligand-Binding Immunoassay team in a regulated Good Laboratory Practices (GLP) setting to support Pfizer�s vaccine programs. You will perform Luminex assays to support toxicology and clinical studies across multiple programs. | 04/30/2021 |
| 8857 | Meridian Medical Technologies Pearl River, NY Associate Scientist, Biofunctional Assay Development Bachelor's Degree. Exp: 1+ years |
You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer�s vaccine programs according to Standard Operating Procedures. You will support the technology transfer and integration of new laboratory immunoassays into the cGLP space, support assay validation projects and monitor immunoassay lifecycle. | 04/30/2021 |
| 8858 | Meridian Medical Technologies Groton, CT Associate Scientist, Analytical Chemistry Bachelor's Degree. Exp: Minimum of 6 months |
The Associate Scientist will take an active role in supporting drug development by applying a variety of analytical methodologies to support physical and chemical characterization of drug substances (including raw materials and intermediates) and drug products. Working knowledge and ability to operate analytical techniques such as HPLC-MS, GC-MS, spectroscopy and physical techniques such as particle size and dissolution used for the characterization of pharmaceutical substances and products is desired. | 04/30/2021 |
| 8859 | Meridian Medical Technologies Pearl River, NY Associate Scientist - Robotics and Automation Bachelor's Degree. Exp: 1+ years |
The associate scientist is responsible for the preparation of samples for preclinical and clinical serology studies to support vaccine development & clinical studies. This work will be performed within the Robotics and Automation area of the High-throughput Clinical Immunoassay and Diagnostics (HCID) group within Pfizer Vaccine Research & Development (VRD). The responsibilities include, but are not limited to, performing manual and robotic sample preparation, instrument qualification, and data organization. | 04/30/2021 |
| 8860 | Meridian Medical Technologies St Louis, MO Associate Scientist, Cell Line Development Bachelor?s Degree. Exp: 0-3 years |
The position will be primarily involved in mammalian CLD portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer�s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. | 04/30/2021 |
| 8861 | Precision Medicine Group Houston, TX Technologist I Bachelor?s Degree (Medical technology, Life Sciences, Biology, or other related discipline). Exp: 0-1 years |
Participate in Flow. PBMCs, IF / IHC projects through assay development, validation, and execution in a timely manner. Process clinical samples. Perform assays according to SOPs and support development of new procedures and improvement of existing SOPs. | 04/30/2021 |
| 8862 | Steris Mentor, OH Field Service Engineer Bachelor's Degree in Electrical Engineering or Mechanical Engineering. Exp: one year |
The Field Service Engineer position is an entry-level engineering assignment within the Service Engineering department. Primary responsibilities include; serviceability/reliability reviews, service documentation development, high-level troubleshooting/technical support on a narrow product focus, and initial product training to technical support personnel and service trainers. | 04/30/2021 |
| 8863 | Horiba Piscataway, NJ Product Specialist BS/MS in Physical or Biological Sciences Exp: 0+ Years |
The job of the product specialist is to provide complete technical support to the customer base in order to resolve customer issues and problems. The product specialist will answer customer phone calls and emails to ensure problems are resolved. The product specialist will also install HORIBA products at customer sites. The objectives are to complete assigned tasks in an efficient and timely manner and comply with companies' guidelines: includes customer support, product installations at customer site, product testing as well as QA/QC, service training and technical notes writing. | 5/1/2021 |
| 8864 | Horiba Troy , MI Service Engineer BS in Electrical or Mechanical Engineering, or Equivalent Exp: 0+ Years |
Responsibilities: Installs, start-up, commission, repairs and maintains HORIBA products at customer sites; performs in-house repairs of defective customer equipment. Provides technical assistance to customers and HORIBA departments, including parts and technical question research and assisting with Requests for Quotation. Prepare Field Service Reports with sufficient detail for customer invoicing, warranty charges, labor and materials changers, and policy. Provides engineering with redlined drawings and verbiage as required detailing any field changes implemented. Creation of factory and On-Site Acceptance Documents and Procedures, performing Acceptance Procedures and post-processing data generated from Acceptance Procedures in order to validate design specifications. | 5/1/2021 |
| 8865 | Horiba Sunnyvale, CA Functional Safety Engineer BS in electrical Engineering, Electronics Engineering, or Related Exp: 0+ Years |
Responsibilities: Assisting senior engineers/consultants with various engineering tasks required to support customers� implementation of ISO 26262 for functional safety. Utilizing your existing and new skills to manage challenging stakeholders who can have diverse objectives with pressure to deliver results. Working closely with the existing company electrical/electronic development teams (systems, hardware, embedded software, integration). Coordinating with supplier management teams. Assisting in deliver to time, cost and quality in regard to the functional safety process. | 5/1/2021 |
| 8866 | Horiba Piscataway, NJ Technical Writer BS in Relevant Scientific Discipline Exp: 0+ Years |
Responsibilities: Plan, develop, organize, write and edit operational procedures and manuals. Work with internal teams to obtain an in-depth understanding of the product and the documentation requirements. Produce high-quality documentation that meets applicable standards and is appropriate for its intended audience. Write easy-to-understand user interface text, online help and FAQ�s. Maintain a comprehensive library of technical terminology and documentation. Manage updates and revisions to technical literature. Creating internal work instructions | 5/1/2021 |
| 8867 | ICU Medical Salt Lake City, UT Engineer I, Quality - Service and Pumps BS in Relevant Discipline Exp: 0-2 Years |
The Engineer I, Quality � Service and Repair works in a Quality Systems environment to ensure that the servicing of infusion pumps meet the requirements of ISO 13485-2016, 21 CFR Part 820, and other applicable regulations and standards. They support key areas to maintain an effective Quality System such as: quality operations, complaint investigations, CAPA investigation, risk management, internal audit, service data collection, analysis and trending. The incumbent encompasses a professional that can work within a quality management system and under the guidance of the immediate supervisor/manager to develop the skills, experience and competences to work in a regulated environment and very dynamic role. They complete projects assigned by experienced engineers and managers. Works on projects/matters of limited complexity in a support role while being closely managed. | 5/3/2021 |
| 8868 | ICU Medical Austin, TX Analyst I, Chemistry BS in Chemistry, Chemical Engineering, or Chemical Science Exp: 0-1 Years |
The Chemistry Analyst I will work under direct supervision or be partnered with an experienced analyst to perform wet chemistry analyses, preparation of reagents, standardization of solutions, and instrumentation testing and documentation in a cGMP environment. May be cross-trained to work in other laboratory areas as dictated by the needs of the department. | 5/3/2021 |
| 8869 | Danaher/Integrated DNA Technologies (IDT) Coralville, IA Lab Technician II BS in Relevant Scientific Discipline Exp: 0+ Years |
The Technician II (Synthesis) synthesizes custom oligonucleotides according to the customer�s order. This generally includes synthesis, cleavage, deprotection and QC sampling of the products being made. The Technician II (Purification) purifies custom oligonucleotides according to the customer�s order. This generally includes the sorting, purification, and QC sampling of the products being made. The Technician II (Formulation) formulates custom oligonucleotides according to the customer�s specifications. This generally includes quantification, final packaging, and QC sampling of the products being made. | 5/3/2021 |
| 8870 | Danaher/Integrated DNA Technologies (IDT) San Diego, CA Lab Technician II - SD Manufacturing BS in Relevant Scientific Discipline Exp: 0+ Years |
The�Technician II (SD Manufacturing)�synthesizes, purifies, formulates and ensures the quality of custom oligonucleotides according to the customer�s order and internal specifications. This generally includes, synthesis, cleavage, deprotection, purification, desalting, QC sampling, QC analysis and final packaging and formulation of the oligos and chemical reagents being made.� | 5/3/2021 |
| 8871 | Danaher/Integrated DNA Technologies (IDT) Coralville, IA Technician II - Small Molecule Chemistry BS in Chemistry or Related Exp: 0+ Years |
The Technician II (Small Molecule Chemistry) is responsible for the preparation of quality raw materials for the production of oligonucleotides. | 5/3/2021 |
| 8872 | Danaher/Integrated DNA Technologies (IDT) Coralville, IA Technician II - Quality Control (CQC) BS in Biology, Genetics, Chemistry, or Related Exp: 0+ Years |
The Technician II is responsible for evaluating products in support of all manufacturing areas within Integrated DNA Technologies. This evaluation involves determining the pass/fail status of products by using a wide variety of molecular biology methods and specialized equipment. | 5/3/2021 |
| 8873 | Danaher/Integrated DNA Technologies (IDT) Coralville, IA Order Verification Specialist BS in Relevant Scientific Discipline Exp: 0+ Years |
Responsibilities: Visually inspects and reviews products prior to shipment to ensure it meets customer specifications. Verifies GMP orders by confirming information from multiple sources, ensuring 100% compliance via an oligo master record with final signoff upon order verification. Troubleshoots any order issues identified during post synthesis review that may prevent shipment. Makes independent decisions regarding a product�s path based on individual attributes of the product and customer requirements. Reviews and documents procedures used for each product in custom software or by other controlled methods. | 5/3/2021 |
| 8874 | Danaher/Integrated DNA Technologies (IDT) Redwood City, CA Research Scientist II MS in Biology, Chemistry, Genetics, or Related Exp: 1+ Years |
The Research Scientist II, under minimal supervision, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with development and characterization of new IDT genomics products in NGS, qPCR and functional genomics. This position is responsible for planning and executing experiments, analyzing data and reporting/presenting findings as well as supporting IDT customers. | 5/3/2021 |
| 8875 | Danaher/Integrated DNA Technologies (IDT) Coralville, IA Bioinformatics Scientist I BS in Computer Science, Biology, Engineering, or Related Exp: 0+ Years |
The Bioinformatics Scientist I, under minimal supervision, will support a group of experienced scientists to develop novel genomic applications. �This individual will be a contributor to the product development team and report to their Bioinformatics group leader. | 5/3/2021 |
| 8876 | Illumina San Francisco, CA Mechanical Engineer I BS/MS in Mechanical Engineering Exp: 0-2 Years |
The Mechanical Engineer 1 will play a key role in manufacturing sustainment and new product introduction of world-class DNA sequencing instruments. Under the supervision of senior engineers, you will design and build test fixtures, perform qualification testing of critical mechanical components and sub-assemblies, and contribute to continuous improvement projects, while interfacing with other functional teams in Hayward, Foster City, San Diego, and Singapore. Not to mention, collaborate with external suppliers and contract manufacturers who build our submodules. | 5/3/2021 |
| 8877 | Illumina San Diego, CA Associate Scientist I MS in Biochemistry, Chemistry, Biological Science, Physical Chemistry, or Related Exp: 1-3+ Years |
This is a hands-on, independent position where the incumbent is responsible for the design and execution of experiments for product/process optimization, development/optimization of analytical methods, and qualification and/or validation activities ensuring the successful technology transfer into a GMP manufacturing environment. | 5/3/2021 |
| 8878 | Illumina San Diego, CA Research Associate I - Consumables Product Development BS/MS in Biology, Biochemistry, Molecular Biology, Chemistry, Bioengineering, or Related Exp: 1-2 Years |
As a Research Associate 1 at Illumina, you will work in a dynamic, collaborative environment and help the reagents/assay team in the development of core platform consumables to create cutting edge and robust new products. You will participate in the development of both analytical and high-throughput assays and processes. You will work in a fast-paced environment with multi-disciplinary teams, design and execute experiments, analyze data and communicate results and progress. Your work on reagent formulation, characterization, stability optimization, workflow development, and various assays and will enable project teams to make critical decisions during a product development cycle. | 5/3/2021 |
| 8879 | Illumina San Diego, CA Metrology Engineer, Integrated Devices Group BS/MS in Biomedical Engineering, Physical Chemistry, Applied Physics, Materials Science, Chemical/Electrical Engineering, Biophysics, or Related Exp: 0-2+ Years |
Responsibilities: Support a wide range of consumable development efforts, including demonstrating the viability of new designs, evaluating process changes/improvements, and resolving urgent issues with on-market products. This may initially be in the areas of nanofabrication and surface chemistry but has the potential to also extend to other consumable technologies. Engage in development efforts with statistically rigorous experimental design and data analysis. This role has a specific emphasis on supporting investigations through laboratory measurements and data aggregation. Evaluate, optimize, and introduce new measurement systems to consumable research and development teams. Actively participate in transferring characterization tools to consumables manufacturing, including demonstrating tool robustness, designing prototype measurement workflows, and training manufacturing process engineers to own systems after transfer. | 5/3/2021 |
| 8880 | Illumina San Diego, CA Research Associate II MS in Biochemistry, Chemistry, Biological Science, Physical Chemistry, or Related Exp: 1-3+ Years |
This is a hands-on, independent position where the incumbent is responsible for the design and execution of experiments for product/process optimization, development/optimization of analytical methods, and qualification and/or validation activities ensuring the successful technology transfer into a GMP manufacturing environment. | 5/3/2021 |
| 8881 | Illumina San Diego, CA Bioinformatics Scientist MS in Bioinformatics, Biology, Engineering, Physical Science, Statistics, or Related Exp: 0+ Years |
Responsibilities: Design, prototype, implement, and test computational algorithms that utilize both statistical and machine learning approaches. Software optimization at the design, algorithm, and source code level. Identify opportunities to improve the bioinformatics user experience and implement solutions.Collaborate with internal project teams and with external organizations. Contribute to the bioinformatics open source community. | 5/3/2021 |
| 8882 | Illumina San Diego, CA Integration Research Associate I BS/MS in Molecular Biology, Biochemistry, or Related Exp: 0-2 Years |
As an Integration Research Associate 2 in Illumina�s Systems Integration group, you will work as part of a multi-disciplinary team to develop and integrate assay workflows for Dx platform verification and validation. | 5/3/2021 |
| 8883 | Grifols Los Angeles, CA QC Chemist 2 - Methods Development and Validation BS in Chemistry, Biochemistry, Biology, or Related Exp: 0+ Years |
The QC Chemist is responsible for performing routine and non-routine chemical and biochemical assays on protein-based therapeutics and raw materials. Responsibilities: Perform various QC / Quality Control testing (i.e. product release testing, stability testing, in-process testing, and other protocol testing) as directed by the laboratory supervisor or senior chemist. Compile and enter data into computer database (i.e. LIMS - Laboratory Information Management System) to be used for reporting and trending purposes. Review test results against specifications. | 4/23/2021 |
| 8884 | Grifols Lafayette, LA Field Service Engineer I BS in Engineering, Technical, or Related Scientific Discipline Exp: 0+ Years |
Responsibilities: Compliance - Adhere to procedures and protocols outlined by the Grifols GST organization and Grifols Diagnostic Solutions. Customer Service – Respond to customer inquiries and complaints, participate in customer site evaluations, upgrades of hardware and/or software, product installations, preventive maintenance, and ongoing service and support for all equipment at the customer facility and via telephone. Documentation of activities within CRM system. Escalation of Customer Needs - openly communicate with other groups within Grifols to assure rapid resolution of issues raised by customers. Projects - will communicate integrally with Global Service and Training (GS&T) and Account Managers regarding product performance, participation in development teams and process development and improvements. | 4/23/2021 |
| 8885 | Grifols Emeryville, CA Manufacturing Associate I BS in Biological or Physical Science Exp: 1-3 Years |
This manufacturing associate position is responsible for the production of recombinant antigens, peptides and or buffers. Specific responsibilities: Provides necessary support for all production activities associated with the Antigen production work. Operates complex antigen production equipment. Participates in equipment and process qualification and troubleshooting. Maintains the production areas and all equipment in clean and orderly operating condition in accordance with cGMP, ISO and Grifols quality and safety standards. | 4/23/2021 |
| 8886 | Grifols Clayton, NC Manufacturing/Maintenance Engineer I BS in Engineering Exp: 0-2 Years |
Responsibilities: Performs routine duties that require application and knowledge of basic engineering principles. Completes small projects/assignments of limited scope and complexity. Prepares plans, designs, calculations, and cost estimates, under close supervision. Interprets engineering specifications and solves routine problems by applying defined procedures and recognized and generally accepted good engineering practices. Provides routine technical support with limited responsibility and accountability. | 4/23/2021 |
| 8887 | Grifols Clayton, NC Automation Engineer MS in Automation, Computer, Industrial, or Manufacturing Engineering Exp: 0-1+ Years |
The Automation Engineer I is an entry level professional who is responsible for using technology to improve and streamline a manufacturing process through automation. Depending on their specific assignment, this person provides automation support for projects or within a specific area or provide validation support for automation projects. The Automation Engineer I can also integrate into a project team. The incumbent is knowledgeable in Automation with the capability to learn specific control systems, instrumentation, process, utilities, or qualification testing. He/she supports meeting customer needs and business goals. In addition, he/she will collaborate with other automation engineers. | 4/23/2021 |
| 8888 | Grifols Emeryville, CA Associate Scientist II MS&T I MS in Biology, Microbiology, Biochemistry, or Related Exp: 0+ Years |
The Manufacturing Organization supports the Technical Operations (TechOps) business by compliantly and successfully producing products in line with commercial cGMPs. The Upstream Associate Scientist II position is a laboratory-based position within the MS&T team. The primary purpose of this position is to work with Senior level associates to develop robust Upstream processes in support of developing and optimizing production processes including process parameter optimization, process characterization, scale-up/tech transfer for large scale product production and support successful implementation of production processes at commercial scale. | 4/23/2021 |
| 8889 | Grifols Emeryville, CA QC Analyst BS in Relevant Scientific Discipline Exp: 1-3 Years |
The QC Analyst will be asked to provide expertise to their designated QC group for the purpose of supporting both manufacturing and quality assurance in the production, release, and monitoring of established product lines. | 4/23/2021 |
| 8890 | Gro Biosciences Cambridge, MA Automation Engineer BS/MS in Biology, Microbiology, Biotechnology, Synthetic Biology, Systems Biology, Biological Engineering, or Related Exp: 0-1+ Years |
The candidate for this position will be instrumental in developing GRO’s new biofoundry. You will work in partnership with skilled scientists and engineers to accelerate their research through a variety of automation platforms. Your creativity and ingenuity will be crucial for all of GRO’s research priorities, including developing new products, optimizing strain performance, and evolving novel amino acid platforms. | 4/23/2021 |
| 8891 | Guerbet Cincinatti, OH Operations Quality Manager BS/MS in a Relevant Technical Discipline Exp: 0+ Years |
Responsibilities: Manage quality support for operations including device history record and batch release processes. Drive measurable quality improvements in support of operations. Manages quality, compliance, and timely closure of complaints through manufacturing investigations. Supervises Quality Engineers and Specialists that process complaints about the site. Oversees, coordinates, and participates in elements of investigations regarding customer complaints. | 4/23/2021 |
| 8892 | Guerbet Cincinatti, OH Electrical Engineer, Urology BS/MS in Electrical Engineering Exp: 0+ Years |
The Electrical Engineer is responsible for the design and development of electrical circuits, and electrical/electronic components for medical devices. The individual will have responsibility for full electrical design life cycle engineering and post development support for new and existing products. | 4/23/2021 |
| 8893 | Guerbet Raleigh, NC QC Lab Coordinator BS in Chemistry or Related Exp: 0-2 Years |
Responsible for inventory management of reagents and consumables, sample receipt and tracking, and various laboratory support tasks including, but not limited to, reagent preparation, housekeeping duties, and equipment maintenance. The Lab Coordinator must be self-motivated, organized, and flexible and able to work under deadlines in a fast-paced environment. | 4/23/2021 |
| 8894 | Gyroscope Therapeutics King of Prussia, PA QA Officer BS in Relevant Scientific Discipline Exp: 1+ Years |
The Quality Assurance Officer will be critical in supporting Gyroscope’s Quality Management System . This role will be responsible of providing day-to-day assistance for QA activities, including the effective execution of overall Gyroscope’s QMS, with focus in supporting Clinical QA. | 4/23/2021 |
| 8895 | Harpoon Therapeutics San Francisco, CA Research Associate, Biology BS/MS in Cell Biology, Biochemistry, or Related Exp: 1+ Years |
Responsibilities include testing of samples in support of both preclinical development and clinical programs, assay development and optimization, and collection of data in support of regulatory filings. Applicants should be capable of working flexibly and expeditiously in a collaborative, innovative and inspiring environment. The ideal candidate will have experience with mammalian cell culture, stable cell line generation, luciferase assays, flow cytometry, and bioassay automation. Good communication skills, good planning, and an ability to meet deadlines are essential. | 4/23/2021 |
| 8896 | Harvard Bioscience Holliston, MA Technical Support Engineer, Neuroscience BS/MS in Neuroscience or Related Exp: 0+ Years |
The individual will be essential in supporting Technical Support colleagues and engineering about product function, user requests, product improvements and product maintenance. This person will engage heavily with the Global Marketing team in the design of products from the perspective of the customers and liaise with engineering for execution of customization to standard products. Provide pre and post-sales support to distributors, subsidiary offices, customers and outside sales force. This role also requires support of repairs, which may include diagnostics and repair. Ultimately significantly contribute toward the sales growth of Harvard Bioscience through appropriate customer communication and follow through. | 4/23/2021 |
| 8897 | Harvard Bioscience Holliston, MA Senior Manufacturing Engineer BS in Relevant Engineering Discipline Exp: 0+ Years |
The qualified candidate will work within a multi-disciplinary team of engineers on DFM, cost reduction, and transfer to production activities. Work closely with assemblers and production leaders to improve manufacturability. Investigate quality issues for engineering improvements. | 4/23/2021 |
| 8898 | Health Decisions Remote , -0 Clinical Research Associate BS in Relevant Scientific Discipline Exp: 0+ Years |
The CRA will be responsible for performing on-site monitoring visits for various client studies to ensure patient safety, GCP compliance and data integrity by confirming the site is conducting the study in accordance with the protocol, ICH guidelines, and applicable regulatory requirements. | 4/23/2021 |
| 8899 | HeartFlow Austin, TX Imaging Analyst BS in Relevant Scientific Discipline Exp: 0+ Years |
The Medical Imaging Case Analyst is responsible for creating computer 3D models of coronary arteries from cardiac medical imaging (CT scans). These 3D coronary artery models show how narrowings and blockages impact blood flow. Creation of the model is done through the use of HeartFlow developed software and processes. In this role, you will work within an operations team to process individual models on a recurring basis. A variety of backgrounds, including but not limited to: radiology, medical technicians, biological sciences, 3D animation, and/or CAD/visual inspection may qualify for this position. | 4/23/2021 |
| 8900 | Helixbind Boxborough, MA Research Associate BS in Molecular Biology or Related Exp: 0+ Years |
Responsibilities: Self-manage assigned projects under supervision from company management. Develop and optimize protocols at the bench scale transitioning to automation. Confer with management and other scientists to adapt and streamline translational processes. Assist in product realization efforts and maintain a consistent review process to meet/exceed expectations. | 4/23/2021 |
| 8901 | Helixbind Boxborough, MA Engineering/Service Technincan BS in Relevant Engineering Discipline Exp: 0-2 Years |
The Engineering Technician will work to maintain, troubleshoot and repair medical diagnostic instruments, commission new equipment, through quality service and professionalism. We are seeking hard working, motivated, and well-organized individuals with a focus on continuous product improvement to exceed expectations. | 4/23/2021 |
| 8902 | Helixbind Boxborough, MA Mechanical/Biomedical/Instrumentation Engineer BS in Mechanical, Electromechanical, Biomedical, or Instrumentation Engineering, or Related Exp: 0-5 Years |
As a member of the engineering design and development team, the preferred candidate will problem solve and participate in the specification, design, build and testing of a diverse range of medical disposables and instruments. | 4/23/2021 |
| 8903 | Helixbind Boxborough, MA Formulation Technician BS in Relevant Science or Engineering Discipline Exp: 0-5 Years |
The formulation technician will manage the production inventory, produce/fill/seal builds of reagents into HelixBind’s proprietary disposable test cassette, will actively communicate with management and co-workers and will maintain a safe, organized, and clean work environment. | 4/23/2021 |
| 8904 | Helomics Pittsburgh, PA Laboratory Technologist BS in Biological or Related Scientific Discipline Exp: 1+ Years |
This position will contribute to tissue culture related activities involved with delivering high quality cells for use in assay development, High Throughput Screening, High Content cell-based assays, compound profiling, technology evaluations, and other objectives requiring delivery and maintenance of live cell cultures and/or frozen cell banks. These activities will be in addition to the other standard aspects of clinical lab testing. | 4/23/2021 |
| 8905 | Hemo Bioscience Durham, NC Manufacturing Technologist BS in Relevant Scientific Discipline Exp: 0+ Years |
The Manufacturing Technologist personnel participate in all non-analytical activities related to the manufacturing of Hemo bioscience products. This position is responsible for following standard operating procedures, best laboratory practices, current good manufacturing practices (cGMP), and current good documentation practices (cGDP) to ensure products are manufactured and systems are maintained to meet internal and customer specifications. | 4/23/2021 |
| 8906 | Heraeus Dayton, OH Quality Engineer - Chemical Production BS/MS in Chemistry or Related Exp: 1-2 Years |
Responsibilities: Facilitates the investigation and response to customer complaints and internal issues. Determine and eliminates root causes and diminish defect occurrences or quality incidents in the process. Supports the Quality Manager with internal and external audits, customer surveys, and respond or resolve corrective and/or preventive actions and verifications. Develops new approaches to solve problems identified during quality assurance activities. Supports the Quality Assurance group in streamlining Quality documentation. | 4/23/2021 |
| 8907 | Heraeus Chandler, AZ Quality Engineer BS in Engineering Exp: 0+ Years |
The primary responsibility of this position is to plan and conduct activities concerned with the quality assurance of industrial processes, materials, and products. Specific responsibilities: Perform routine inspections on CMMs and program as needed. Plans and conducts activities concerned with the quality control and quality assurance of industrial processes, materials and products. Facilitate and maintain gage calibration process for entire organization, calibration of gages and assists in formulating calibration standards (including GR&R studies). | 4/23/2021 |
| 8908 | Heska Des Moines, IA Research and Development Scientist BS/MS in Microbiology or Related Exp: 0+ Years |
The incumbent will assist the R & D Manger in the successful development and completion of experiments and studies aimed at supporting USDA licensure of veterinary biological products. Plan and execute scientific studies leading to the development and introduction of products, process and product control, and improved methods specific to the optimization of animal vaccine production. May develop in-process assay methodologies as needed and will assist in the validation of new final product assays. | 4/23/2021 |
| 8909 | Hexagon Bio Menlo Park, CA Research Associate, Natural Products Chemistry BS in Chemistry, Biochemistry, Biology, or Related Exp: 0+ Years |
As a research associate on the natural products chemistry team, you'll join a team of experienced natural products scientists to isolate novel molecules generated by Hexagon Bio's synthetic biology platform. Through your primary responsibility of performing extractions and purifications, you will be exposed to a variety of techniques including mass spectroscopy, chromatography, and automation methods related to natural product chemistry. | 4/23/2021 |
| 8910 | Hexagon Bio Menlo Park, CA Research Associate, Cell Biology and Drug Discovery BS in Biology or Equivalent Exp: 1+ Years |
At Hexagon, you will be an integral part of a dynamic interdisciplinary team focused on developing next generation medicines. You will use your strength as an experimentalist to assist in designing, developing and optimizing target specific cell assays. You will work with senior scientists to plan, execute, and analyze your experiments and present your results. | 4/23/2021 |
| 8911 | Hikma Cherry Hill, NJ Manufacturing Specialist BS in Relevant Discipline Exp: 0-3 Years |
The Manufacturing Specialist will assist the shift lead in a hands-on approach to overseeing production activities including, filling, sterilization, component and equipment prep, and compounding. Completes quality systems activities including commitments, deviations, DCEs, and SOP revisions as necessary. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing recommendations. Interprets manufacturing policies, procedures, and programs.The Manufacturing Specialist will assist the shift lead in a hands-on approach to overseeing production activities including, filling, sterilization, component and equipment prep, and compounding. Completes quality systems activities including commitments, deviations, DCEs, and SOP revisions as necessary. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing recommendations. Interprets manufacturing policies, procedures, and programs. | 4/23/2021 |
| 8912 | Hikma Cherry Hill, NJ Associate Scientist BS in Relevant Science or Engineering Discipline Exp: 0+ Years |
This position supports the parenteral pharmaceutical manufacturing facility through the qualification and/or validation of equipment, raw materials, and manufacturing processes. Validation activities include research, protocol writing/execution and final report generation. Additionally, investigations of manufacturing challenges are conducted and process improvements are evaluated/implemented. Final documents are archived and may be included in or support A/NDA submissions, and made available as needed during FDA, MHRA, and client/customer compliance audits. | 4/23/2021 |
| 8913 | Hikma Columbus, OH Scientist I, QC Microbiology BS in Relevant Scientific Discipline Exp: 1-3 Years |
Individual is responsible for making sure that all products, raw materials and the environment for production are micro-biologically acceptable while ensuring regulatory compliance standards and release times are met. | 4/23/2021 |
| 8914 | Hikma Cherry Hill, NJ Quality Lab Associate I, Env. Monitoring BS in Biology or Microbiology Exp: 0-2 Years |
The individual is responsible for performing functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. | 4/23/2021 |
| 8915 | Hikma Cherry Hill, NJ Quality Lab Associate III, Chemistry MS in Chemistry or Related Exp: 1-4 Years |
Responsibilities; Conduct chemical, biochemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming components and raw materials to finished goods and stability. Perform laboratory investigations for OOS results or other exceptions. Proficiently uses analytical instrumentation and troubleshoots equipment issues. Execute validation for laboratory instruments and methods and conducts routine/non-routine testing. Write/ revise standard operating procedures, protocols, test methods and change controls as needed. Works independently. | 4/23/2021 |
| 8916 | Hikma Columbus, OH Scientist I, Quality Control - Nasals BS in Chemistry or Related Exp: 1+ Years |
The scientist schould expect to perform routine, work-flow processes within the quality control laboratory to meet customer requirements by supporting the testing of raw materials and finished products while ensuring regulatory compliance standards and release times are met. | 4/23/2021 |
| 8917 | Hikma Columbus, OH Scientist I, QC Aero Starting Materials BS in Chemistry or Related Exp: 1+ Years |
The scientist schould expect to perform routine, work-flow processes within the quality control laboratory to meet customer requirements by supporting the testing of raw materials and finished products while ensuring regulatory compliance standards and release times are met. | 4/23/2021 |
| 8918 | Hillrom St. Paul, MN Manager, Medical Affairs MS in Clinical Informatics or Related Exp: 1+ Years |
Responsibilities: Develop clinical plans for respiratory health to build clinical evidence for key clinical value propositions addressing short term as well as longer term needs through various forms of research including review articles, health outcomes research, post-marketing studies, and clinical trials to support regulatory submissions (PMA, IDE, 510(k)). Serve as the clinical expert with primary focus on the product lines interacting with marketing, regulatory, and research & development to ensure clinical activities are aligned with business objectives. | 4/23/2021 |
| 8919 | Hillrom Batesville, IN Engineer II R&D BS in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Agricultural Engineering, or Related Exp: 1 Year |
Responsible for technical design changes and projects in the R&D Sustaining Engineering Department to modify and maintain FDA Class I and Class IIa products – Hospital Beds and Surfaces. Provides technical contribution within the mechanical engineering discipline to lead design changes, requirement specifications, analysis, and verification & Validation activities to meet internal and external customer requirements. | 4/23/2021 |
| 8920 | Hillrom Batesville, IN Product Quality Engineer BS in Quality, Industrial, or Mechanical Engineering Exp: 0+ Years |
The Product Quality Engineer is responsible for supporting the quality and regulatory related matters associated with the medical bed devices at the Hill-Rom Batesville Manufacturing site. This position will also be responsible overseeing and/or assisting with a variety of Quality Engineering functions and ensuring compliance with QSR regulations and Hill-Rom policies and procedures. In addition, this position will work to provide the necessary data to make effective quality and business decisions, and implement sound, data-driven quality and business solutions that emphasize quality system compliance. | 4/23/2021 |
| 8921 | Homology Medicines Bedford , MA Clinical Project Coordinatior BS in Nursing, Biology, Biochemistry, or Related Exp: 1-3 Years |
The Clinical Project Coordinator (CPC) will be responsible for assisting the study team in running the day to day operational activities of clinical studies. The individual will be responsible for the coordination, tracking and management of daily activities for multiple clinical studies to support both the internal team and Clinical Research Organizations (CROs). | 4/23/2021 |
| 8922 | Hookipa Pharma New York, NY Clinical Trial Associate - Clinical Operations BS in Relevant Scientific Discipline Exp: 0+ Years |
HOOKIPA is seeking a Clinical Trial Associate (CTA) to support trial managers in the planning and implementation of clinical trials. The CTA will work collaboratively within study teams and across functional areas, under the guidance of a clinical trial manager. This position can be considered as an entry level position. Direct prior experience in the field of clinical research is welcome but is not required. The CTA position is a great learning experience designed to introduce a new team member to managing clinical trials at a biopharmaceutical company and is a stepping stone for further development in the clinical trial operations field. The successful candidate will be an organized self-starter with a collaborative attitude, willingness to learn from mentors, and have the ability to complete project tasks with attention to details. | 4/23/2021 |
| 8923 | Ascent Pharmaceuticals Central Islip, NY Quality Control - QC Chemist Bachelor’s degree or foreign equivalent in Pharmacy/Chemistry or related field. Exp: 1 year |
Analyze and test raw materials, in-process and finished product samples using modern quality control techniques; develop, validate and test analytical methods for analytical pharmaceutical ingredients (API) and dosage forms; perform QC/development activities using Chromatography, Spectroscopy, HPLC, GC, TLC, Dissolution etc. | 4/20/2021 |
| 8924 | Astellas Pharmaceuticals Seattle, WA Research Associate II, Cell Editing MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Cell Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. This position will be provided training to perform all required fundamental skills. | 4/21/2021 |
| 8925 | Astellas Pharmaceuticals Westborough, MA QC Analytical Associate II, Cell Therapy MS Exp: 0-2 years |
This position provides Quality Control qualification, validation, testing support for AIRM cell therapy products. Looking for strong GMP background with method validation and quality control testing experience. | 4/21/2021 |
| 8926 | Astellas Pharmaceuticals Seattle, WA Research Associate I, Cell Editing BS degree Exp: 0-3 years |
The primary purpose of the Research Associate I for Cell Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This entry-level Research Associate role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. This position will be provided training to perform all required fundamental skills to include record keeping, aseptic technique/cell culture, general lab operations, equipment use and maintenance, and some troubleshooting. | 04/21/2021 |
| 8927 | Aurora Biolabs San Diego, CA Research Associate I BS/MS Exp: 0-1 year |
The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. | 04/21/2021 |
| 8928 | Axcella Health Cambridge, MA Research Associate Masters Exp: 1+ years |
Provide support to the Research Team to advance compound mechanism of action understanding in primary human cell culture and translational bio-specimens. | 04/21/2021 |
| 8929 | Axial Therapeutics Waltham, MA Research Associate, Biology Bachelor’s degree in biology, biochemistry or a related field preferred. Exp: 1-3 years |
The Research Associate will support biology as a member of a highly matrixed drug discovery team and will be responsible for the execution and troubleshooting of various biological assays and experiments. | 04/21/2021 |
| 8930 | Axis Clinicals USA Dilworth, MN Analytical Chemist I Bachelor’s degree in Biology, Chemistry, or equivalent. Exp: 1 year |
The Analytical Chemist I, Bioanalytical Operations carries out various Bioanalytical functions of the organization. The Analytical Chemist is responsible for executing Bioanalytical methods within AXIS Clinicals. | 04/21/2021 |
| 8931 | BioDuro San Diego, CA Reasearch Associate I/II, Oncology BS in biology-related fields or equivalent experience. Exp: 1 year |
The In-Vivo Research Associate is responsible for implementation of in vivo and in vitro studies through animal handling in a vivarium or laboratory environment; including compound administration by multiple routes – dosing, tumor implantation and measurement, harvesting tissues and blood samples. | 04/21/2021 |
| 8932 | BioNano Genomics San Diego, CA Research Associate, Assays and Reagents (Tech Dev) BS in Biochemistry, Molecular Biology or a related field. Exp: 1 year |
The Research Associate position requires a hardworking, team oriented and meticulous person with outstanding laboratory and communication skills. He or she should demonstrate traits consistent with the company culture: drive and perseverance in accomplishing goals, a sense of responsibility and integrity, effectiveness as a team member, adaptability to new projects; strong planning and organizational skills, resourcefulness, determination and motivation to undertake and complete tasks, and enthusiasm for both the business and their work. | 04/22/2021 |
| 8933 | Novozymes RTP, Raleigh-Durham, NC Research Associate/Sr. Research Associate, Microbial Development Master's Degree in a scientific discipline. Exp: 0+ |
You could be our next colleague in Microbial Development. As Research Associate/Sr. Research Associate, you will be responsible for the generation of cell banks that are used by our microbial production facilities worldwide. | 04/22/2021 |
| 8934 | Bio-Technical Resources Manitowoc, WI Assistant Research Scientist, Analytical Support A BA, BS or MS in analytical chemistry, biochemistry, or chemical engineering. Exp: 1-3 years |
In addition to a background in chemistry, the successful candidate will have a strong understanding of microbiology. Seeking an Assistant Research Scientist to work with supervision as an analytical research assistant supporting teams developing fermentation and biotransformation processes for the production of antibiotics, enzymes, proteins, chemicals, and metabolites. The position involves implementation of HPLC, chromatography, enzyme assays, and gel-based analytical methods. Common tasks include analytical separations and quantitative analyses by: 1) HPLC and column chromatography including affinity chromatography, IEX, HIC, and SEC; 2) spectrophotometric enzyme assays; 3) sample preparation and extraction; and 4) basic antibody and protein analyses, using ELISA, protein extraction, protein concentration assays, SDSPAGE, and Western blot. | 04/22/2021 |
| 8935 | Bio-Technical Resources Manitowoc, WI Microbiologist/Molecular Biologist A BA, BS, MS, or Ph.D. in microbiology with a molecular biology emphasis is required. Exp: 1-3 years |
The position involves generating and improving strains using strain engineering molecular biology techniques or classical mutagenesis, screening and selection. Routine microbiology tasks include: 1) media preparation and sterilization; 2) aseptic microbial strain maintenance and handling; 3) preparation of master and working cell banks; 4) setting up and carrying out shake flasks experiments and sampling; 5) harvesting of biomass and/or cell-free supernatant; and 6) analytics, such as growth curves, enzyme assays, and plating for enumeration of microbes. | 04/22/2021 |
| 8936 | Biotium Fremont, CA Chemistry Technician I (CHEMISTRY) B.S. or M.S. degree in Chemistry. Exp: 1+ |
Under the direct supervision from senior chemist, perform chemical purifications using chromatography including preparative HPLC or gravity chromatography; carry out chemical synthesis using standard protocols; carry out chemical analyses using modern instruments including analytical HPLC, LC-MS, TLC, UV/Vis and fluorescence spectrophotometry. | 04/22/2021 |
| 8937 | Biotium Fremont, CA Research Associate, Process Development B.S. in Biochemistry, Biology or a related field. Exp: 1+ years |
This role will be responsible for scale-up of protein purification processes in order to generate milligram to gram-scale quantities of recombinant proteins to support life science reagent manufacturing. The successful candidate will be highly proficient in recombinant protein expression and purification from various host cell systems (e.g. E. coli and mammalian cells). | 04/22/2021 |
| 8938 | Biotium Fremont, CA Research Associate, Molecular Biology B.S. in Molecular Biology, Biochemistry or a related field. Exp: 1+ years |
This role will be responsible for performing production-scale nucleic acid purifications and nucleic acid detection using fluorescence assays and quantitative PCR. The successful candidate will have experience handling DNA and RNA, and be capable of demonstrating careful pipetting technique in sensitive assays. This individual will play an important supporting role in the design, optimization, and assessment of new nucleic acid detection products. | 04/22/2021 |
| 8939 | BlueRock Therapeutics Toronto, Ontario, CA Process Specialist II/Sr. Process Specialist Master's Degree in engineering, life sciences or related field. Exp: 0 – 3+ years |
We are looking for an MSAT Process Specialist II/Senior Process Specialist, reporting to the Senior Manager MSAT, to provide process improvement and technical support for technology transfers, scale-up/scale out, process understanding and GMP manufacturing. Additionally, draft and review protocols, standard procedures, and process summary reports, and provide technical assessment for internal and external collaborators on process changes as well as documentation pertaining to process development, characterization, and validation to meet regulatory requirements. | 04/22/2021 |
| 8940 | BlueRock Therapeutics Cambridge, MA Research Associate I/II, Immunology (Macrophage) Bachelor’s degree in Immunology, Immuno-Oncology or related discipline. Exp: 1+ year (RA I) |
The successful candidate will have hands on experience in Immunology and immune cell biology. This individual will join a team of scientists to engineer novel immune cell therapies derived from induced Pluripotent Stem Cells (iPSC) for the treatment of inflammatory or autoimmune diseases. | 04/22/2021 |
| 8941 | BlueRock Therapeutics Cambridge, MA Research Associate, Genome Engineering (Gene Editing) M.Sc. in cell biology, molecular biology, genetics or related discipline. Exp: 0+ years |
The incumbent will be a technical contributor in a dynamic and progressive team pioneering the generation of genome-modified therapeutic cells from human pluripotent stem cells (hPSCs). Together with technical staff and direction from the Senior Scientist, the individual will contribute to the design and execution of a variety of genetic modifications that enhance cellular properties. | 04/22/2021 |
| 8942 | BlueRock Therapeutics New York, NY Research Associate I, Assay Discovery and Development Bachelor's in Biological Sciences. Exp: 0-2 years |
The candidate will be a key technical contributor of a dynamic and progressive team pioneering scaled somatic cell manufacturing processes utilizing state-of-the art culturing technology at increasing scales. The successful candidate will drive assay discovery and development at BlueRock, NY, establishing critical characterization and quality assays for cell therapy products and manufacturing processes with minimal supervision. Expertise in cell and molecular biology is required. | 04/22/2021 |
| 8943 | BlueRock Therapeutics New York, NY Research Associate I/II, Genome Engineering (Gene Editing) M.Sc. in cell biology, molecular biology, genetics or related discipline. Exp: 0+ years |
The individual will contribute to the design and execution of a variety of genetic modifications that enhance cellular properties. This will include the employment of gene editing technologies including homologous recombination and CRISPR/Cas to establish cell lines for BlueRock’s research pipeline that are altered in their genome to provide novel morphology or function. | 04/23/2021 |
| 8944 | BlueRock Therapeutics New York, NY Research Associate II/Sr. Research Associate , In Vivo Sciences (Neurology) Masters in biological sciences. Exp: 0-6 years |
The successful candidate will be a key technical contributor of a dynamic and progressive team developing novel therapeutics. This challenging opportunity requires in depth knowledge of neurodegenerative diseases as well as stem cell biology. The ideal candidate will be a highly motivated individual who leads from the bench and enjoys having broad responsibilities and opportunities. | 04/23/2021 |
| 8945 | Visby Medical San Jose, CA Lab Technician Bachelor's degree in a scientific field preferred. Exp: 1-2 years |
The Laboratory Technician will be responsible for providing laboratory support for research and product development. The Technician will perform a variety of duties in support of research goals, objectives, and protocols. | 04/23/2021 |
| 8946 | Boston Analytical Salem, NH Microbiologist BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The QC Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 04/23/2021 |
| 8947 | Boston Heart Diagnostics Framingham, MA Medical Technologist Bachelor's degree in one of the chemical, physical or biological sciences. Exp: 1+ years |
Performs clinical laboratory procedures and examinations and any other tests or procedures conducted by a clinical laboratory, including maintaining equipment and records, and performing quality assurance activities related to examination performance, and which require the exercise of independent judgment and responsibility, as determined by the department. | 04/23/2021 |
| 8948 | CareDx Brisbane, CA R & D Laboratory Assistant BS/BA in a biology-related science is preferred. Exp: 0-3 years |
R&D Laboratory Assistant (Tuesday through Friday 11:00 AM - 7:30 PM and Saturday 9:00am-5:30pm). The PM shift R&D Laboratory Assistant (RDLA) is primarily focused on receiving and accessioning: the data entry and quality check of patient and sample information in the R&D laboratory information management system (LIMS). A RDLA also performs a variety of laboratory and administrative tasks to support the R&D laboratory staff. | 04/23/2021 |
| 8949 | Abcam Burlingame, CA Research Associate, IVD BS Degree in biochemistry, pathology, cell and molecular biology, immunology or other Life Sciences. Exp: 0-3 years |
You will join a cross-functional team delivering recombinant antibodies for use in immunohistochemistry applications, developed and manufactured under MDSAP/ISO13485 (2016) quality standard. These antibodies are supplied to our customers for use in critical care, serving as diagnostic reagents in pathology settings. The role is based in Burlingame, California and part of the In Vitro Diagnostic (IVD) team, reporting to the Principal Scientist of IVD. | 04/23/2021 |
| 8950 | Abcam Branford, CT Research Associate (6-12 months contract) B.S. in molecular biology, cell biology or a related field. Exp: 1-3 years |
The successful candidate will play a hands-on role in the company’s use of a variety of molecular biology, assay development, and protein purification techniques in support of various commercial and academic customer projects to deliver high-quality and on-time customized recombinant antibodies. | 04/23/2021 |
| 8951 | Abcam Eugene, OR Research Associate - NPD (ftc) B.S. in Biology, or closely related discipline. Exp: 1 year |
Abcam is looking for a full-time contract Research Associate to assist in the development of novel immunoassays in our Eugene, OR facility. The core responsibility will be to provide support to the SimpleStep immunoassay development team through the use of antibody-based laboratory techniques such as sandwich ELISA, Western blot, immunocytochemistry, and flow cytometry as well as the generation of biological materials for analysis. | 04/23/2021 |
| 8952 | AstraZeneca Gaithersburg, MD R&D Associate I - Fermentation - BPD Bachelors degree in Chemical/Biochemical Engineering/Biotechnology/ or relevant field. Exp: 0+ yrs |
Cell Culture & Fermentation Sciences is an arm of the Biopharmaceutical Development Group. We are responsible for developing all of the clinical and commercial processes that use microbial or mammalian cells to generate therapeutic proteins. In this role you will be part of a team of highly skilled scientists working on fermentation projects using multiple microbial hosts. | 04/23/2021 |
| 8953 | AstraZeneca Gaithersburg, MD R&D Associate I - Cell Therapy (CAR-T) - BPD BS in Chemical/Biochemical Engineering, Biotechnology, Biochemistry, Cell Biology, Immunology or Biological Sciences. Exp: 0+ years |
The Cell Culture and Fermentation Sciences Group is accountable for cell line development, process development, and process characterization. This group assists in the scale up and technical transfer of processes to different clinical and commercial sites and also supports manufacturing deviations and regulatory submissions as needed. | 04/23/2021 |
| 8954 | AstraZeneca Gaithersburg, MD R&D Associate I - BPD BS in Chemical/Biochemical/Biomedical Engineering, Biotechnology, Biochemistry, or Biological Sciences. Exp: 0-2 years |
This position within Cell Culture and Fermentation Sciences will involve substantial amount of hands on cell culture work to develop, scale up, and characterize mammalian culture processes. The candidate will be expected to execute experiments on a routine basis to develop and characterize the upstream cell culture processes and be familiar with the basics of DOE including screening and optimization designs. | 04/23/2021 |
| 8955 | Blueprint Genetics Seattle, WA Technologist Medical I Bachelor’s Degree in a biological, chemical or physical science from an accredited institution. Exp: one (1) year |
The Medical Technologist I performs tests requiring the exercise of independent judgment and responsibility in those specialties in which the Technologist is qualified by education, training and experience. | 04/23/2021 |
| 8956 | Bristol Myers Squibb Bothell, WA Biotech Manufacturing Associate I Bachelors in relevant science or engineering discipline. Exp: 0-2 years |
The primary focus of the Manufacturing Associate role will be cellular therapeutic manufacturing at JuMP during process transfers, routine production, and technology improvements. The key deliverables for this role are (1) helping to establish the JuMP manufacturing operations and (2) completing production assignments with a high quality and timely output. | 04/23/2021 |
| 8957 | Bristol Myers Squibb Redwood City, CA Associate Scientist/Senior Associate Scientist, Translational Research M.S. with strong scientific knowledge and research experience in cancer biology or cellular and molecular biology is required. Exp: 1-5 years |
This position will support the identification of potential biomarkers and patient populations, target engagement, and pharmacodynamic assays for oncology targets. Additionally, the position will support mechanism of action studies using primary human tumors and mouse models and platform development and validation studies for TME biology. The qualified candidate is a highly motivated, collaborative, and creative individual th | 04/23/2021 |
| 8958 | Bristol Myers Squibb Redwood City, CA Associate Scientist/Senior Associate Scientist, Immunology Discovery M.S. with experience in immunology and/or immuno-oncology. Exp: 1-5 years |
Will be responsible for conducting, analyzing, and reporting experiments to drive the advancement of early therapeutic targets for cancer immunotherapy specifically in the areas of myeloid and adaptive tumor biology, as well as examining tumor intrinsic mechanisms of immune mediated resistance. This position will have an emphasis on generating relevant data for selection of clinical candidates and will also include early target discovery, validation, and mechanism of action studies for preclinical drug development. | 04/23/2021 |
| 8959 | Covance Indianapolis, IN Research Assistant I - Immunochemistry Bachelor of Science/Arts (BS/BA) degree in related scientific field. Exp: 1- 2 years |
Analyzes biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. | 04/23/2021 |
| 8960 | Covance Greenfield, IN Research Assistant I - Biotech (Protein Chemistry) BS/BA degree in science or related field. Exp: 0+ years |
No Direct Industry Related Experience Required. Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel within the Protein Chemistry group. | 04/23/2021 |
| 8961 | Covance Madison, WI Study Technician (Research Assistant) Pathology Bachelor’s Degree in Life Sciences, or Associate Degree in Histology, Laboratory Animals Technology or Veterinary Technology. Exp: 0+ years |
No professional experience required. You will be performing basic necropsy or histology tasks on a variety of laboratory animals in compliance with the appropriate Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs) and regulatory guidelines. | 04/23/2021 |
| 8962 | Covance Madison, WI Research Associate (I) - Cell and Gene Therapy Master’s degree (MS/MA) in immunology or related scientific field preferred. Exp: 1-3 years’ |
As part of Global I&I department, you will provide support to, Safety Assessment (SA), and standalone studies over a wide range of Immunology and Immunotoxicology platforms, supporting enhanced solutions based approach to Clients’ requests. | 04/23/2021 |
| 8963 | Nitto Denko Avecia Marlborough, MA Research Chemist BA/BS or MS Exp: 1+ years/BS; 0+/ MS |
The Research Chemist is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. | 4/10/2021 |
| 8964 | Avidity Biosciences San Diego, CA Research Associate Bachelors or masters degree in bioengineering, biology, biochemistry, or related discipline. Exp: 1+ years |
Ideal candidate will be excited about creative assay development as well as testing those ideas in the lab. This will require hands-on lab work, including processing and analyzing animal blood and tissues. | 4/10/2021 |
| 8965 | Avidity Biosciences San Diego, CA Research Associate, Chemistry BS/MS in organic chemistry or biochemistry. Exp: 0-3+ biotech; 1-3+ organic synthesis |
This is a hands-on position with responsibility for the design, synthesis, and analysis of antibody oligonucleotide conjugates. The ideal candidate will have biotech/pharma experience in aspects of medicinal chemistry, bioconjugation and nucleic acid therapeutics. | 4/10/2021 |
| 8966 | ChemPacific Corp Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: 1+ year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps. | 4/13/2021 |
| 8967 | CRISPR Therapeutics Cambridge, MA Research Associate I/II, Analytical Development (Biophysical/Mass Spectrometry) B.S./M.S. in Chemistry, Biology, Chemical Engineering, Biochemistry, or related discipline Exp: 0-3 years |
Develop novel gene editing therapies for serious diseases such as hemoglobinopathies, cancer, diabetes, etc. The successful candidate will join the AD (Analytical Development) team in Tech Ops and will work closely with Research, Process Development, Manufacturing, Quality Assurance, and external contract organizations. | 4/13/2021 |
| 8968 | CRISPR Therapeutics Cambridge, MA Research Associate I, Genomics BS or MS in biology or related discipline. Exp: 1+ years |
Develop novel gene editing therapies for serious diseases. Integral in discovering, developing, and characterizing the next generation of genetic therapies for a wide range of indications. | 4/13/2021 |
| 8969 | Exicure Chicago, IL Technical Associate, Platform Research Bachelor’s degree in chemistry, biochemistry, molecular and cellular biology or related science field. Exp: 0-3 years |
This introductory-level position is suited for an individual who: i) is comfortable working in a laboratory setting, and ii) thrives in a team-oriented environment. Responsible for performing in vitro experiments as a member of an interdisciplinary team focused on developing and advancing Spherical Nucleic Acid drug delivery platforms. | 04/13/2021 |
| 8970 | GenEdit San Francisco, CA Research Associate - Preclinical Development B.S. or M.S in Biology, Biomedical Engineering, Cell Biology, Immunology, Pharmaceutical Sciences or a related field. Exp: 1-3 years |
Hands-on experience in performing in vivo preclinical studies to join our team. This full-time position will report to the Senior Scientist, In Vivo Studies, and will be responsible for testing nanoparticle encapsulated gene therapeutic drugs in vivo and related in vitro analysis of tissues and cells. | 04/13/2021 |
| 8971 | Gliknik Baltimore, MD Laboratory Research Associate Bachelor’s degree in cell biology, microbiology, biological sciences, biochemical / molecular cell biology, immunology, or biochemical engineering or Exp: entry-level |
Individuals with an interest in biopharmaceutical drug discovery to learn and conduct laboratory techniques as a laboratory research associate. This position is an entry-level role at Gliknik. | 04/13/2021 |
| 8972 | Immucor Norcross, GA Medical Laboratory Technologist Associate's Degree or a Bachelor's degree with MLT (ASCP) preferred, MT(ASCP) preferred certification designation. Exp: six months to one year |
Open to new graduates with certification pending. Experience in Blood Banking/Transfusion Medicine. As a Medical Technologist, you will perform all assigned tasks following applicable laboratory SOPs, OSHA regulations and cGMP regulations (i.e. blood borne pathogens and chemical hazards). | 04/14/2021 |
| 8973 | Lampire Biological Labs Coopersburg, PA Laboratory Technician B.S. in relevant field or High School Diploma or equivalent. Exp: 1 – 2 years |
To prepare raw, intermediate or final products in accordance with client specifications and/or Lampire work orders with the goal of providing consistent, high quality products and services to our customers with complete and accurate documentation. | 04/14/2021 |
| 8974 | Tanvex BioPharma San Diego, CA Research Associate, Cell Culture Development - #1290 Bachelor’s degree in Chemical Engineering, Biochemical Engineering, Cell Biology, Biochemistry or related scientific disciplines. Exp: 0-3 years |
Responsible for executing individual experiments related to the cell culture process development of biopharmaceuticals, including media preparation, bioreactor setup, cleaning, sterility and operation, maintaining instruments and equipment, examining data and preparing experiment reports. | 04/15/2021 |
| 8975 | Tanvex BioPharma San Diego, CA Research Associate, Bioassay Development - #1286 (6 mos Temp to hire.) Bachelor’s or advanced degree in cell and/or molecular biology, or related scientific discipline . Exp: 0-3 years |
Responsible for biological characterization of Biologics drug candidates including method development, method qualifications, method transfer and training, and routine non-GMP sample testing. | 04/15/2021 |
| 8976 | Tanvex BioPharma San Diego, CA Research Associate, Bioassay Development - #1277 Bachelor’s degree in cell and/or molecular biology or related scientific discipline. Exp: 0-3 years’ |
Responsible for executing experimentation related to biological characterization from method development and sample testing, to method transfer/qualification/validation for support of pipeline projects. | 04/15/2021 |
| 8977 | Tanvex BioPharma San Diego, CA Manufacturing Associate, Upstream - #1288 Bachelor's or advanced degree in life sciences or related discipline. Exp: 0-3 years |
Perform routine manufacturing activities in GMP manufacturing areas including fermentation and/or cell culture and the associated sub-processes/preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. | 04/15/2021 |
| 8978 | Tanvex BioPharma San Diego, CA Senior Research Associate, Analytical Chemistry - #1265 Master’s degree in chemistry, biochemistry, biology, chemical/biochemical engineering, or related scientific discipline. Exp: 0-3 years’ |
Responsible for executing various tests, developing, qualifying, validating/transferring analytical methods with moderate supervision in order to support all CMC activities at Tanvex. This position is instrumental in providing analytical chemistry support. | 04/15/2021 |
| 8979 | Tanvex BioPharma San Diego, CA QC Associate, Microbiology (Temporary) - #1268 (6 mos Temp.) Bachelor’s of Science degree in the field of molecular biology, chemistry, biochemistry, or a related scientific discipline. Exp: 0-3 years |
Performs routine environmental monitoring of GMP manufacturing facilities, assists with trending of environmental monitoring data, and performs routine microbiological testing such as endotoxin, bioburden and sterility. | 04/15/2021 |
| 8980 | Utah Medical Products Midvale, UT Quality Engineer Bachelor's degree (BS) from a four-year college or university. Exp: one year |
1. Manages complaint handling system. 2. Schedules and conducts or reviews internal quality audits. 3. Reviews and maintains records of internal audits and internal corrective actions, and participates in MRB. 4. Responsible for Quality Assurance review of R&D and manufacturing projects. 5. Gathers, prepares and presents appropriate Company Quality Assurance-related reports. | 04/15/2021 |
| 8981 | Advanced Bioscience Labs Rockville, MD Lab Research Specialist - Immun BS Degree/MS Degree Exp: BS 1-3 years/ MS 0-2 years |
Assist in the development and qualification of new immunological assays including; but not limited to, the following: Blood and mucosal sample processing, Multicolor-Flow Cytometry based assays, cytokines and other soluble biomarkers Multiplexing assays (Luminex, MSD platforms), ELISA, ELISpot, and Neutralization Assays, among others. | 04/15/2021 |
| 8982 | Abzena Bristol, PA AMD/QC Analytical Scientist MS Degree in analytical chemistry, chemistry, biology, biochemistry, or related discipline. Exp: 1-3 years |
The principle responsibility of the Analytical Method Development/Quality Control (AMD/QC) Analytical Scientist is analytical support for GMP manufacturing and process development. | 04/15/2021 |
| 8983 | Abenza Bristol, PA BioConjugation Scientist MS in biochemistry, chemistry, protein chemistry or related discipline. Exp: 1-5+ years |
Responsible for contributing to the optimization and development of bioconjugation techniques and related processes, including but not limited to the areas of Antibody Drug Conjugates (ADCs), protein drug conjugates, conjugated vaccine, | 04/15/2021 |
| 8984 | Abenza Bristol, PA Chemistry Scientist MS in Chemistry. Exp: 0-10 years' |
Duty will include day to day management of one or more of Abzena’s chemistry laboratories and the personnel working in these laboratories. The person will be responsible for executing and delivering in a timely manner chemical synthesis projects assigned to you for Abzena’s clients. | 04/15/2021 |
| 8985 | Abenza San Diego, CA Scientist - Virology/Molecular Biology MS in Virology, Cell Biology, Molecular Biology, Biochemistry, Microbiology or related field. Exp: 1-5 years |
Development, technical transfer and validation of cell based viral assays and molecular such as detection of murine, bovine, and porcine viruses, qPCR testing, barcode testing, genetic sequencing, and other methods for lot release and stability as well as Viral Clearance studies. | 04/15/2021 |
| 8986 | Agenus Lexington, MA (Sr.) Research Associate - Preclinical / In Vivo BS or MS degree in molecular, cellular biology, or related discipline. Exp: 1+ years |
The successful candidate is expected to contribute to the discovery, research, and development of novel immunotherapeutic agents to address unmet medical needs of cancer patients. | 04/16/2021 |
| 8987 | AGTC Gainesville Area, FL R&D Associate BS/MS in in biological sciences or related field. Exp: 0-1+ years (R&D Associate I) |
The R&D Associate on the Assay Development Preclinical R&D team is responsible for support of the Assay Development team by developing, qualifying and troubleshooting quantitative, semi-quantitative, and qualitative assays in support of research, nonclinical, and clinical programs. | 04/16/2021 |
| 8988 | Ajinomoto Bio Pharma Services San Diego, CA Analytical Technologies Associate I Bachelor’s degree in a Life Sciences discipline or equivalent. Exp: Zero to 2 (0-2) years |
This position learns and performs assays to transfer/qualify/validate analytical methods and maintain analytical instrumentation. This position is an entry-level position and regularly provides help with technical papers and reports. | 04/16/2021 |
| 8989 | Ajinomoto Bio Pharma Services San Diego, CA Drug Product Manufacturing Associate I Bachelors in a science or engineering discipline preferred. Exp: zero to two (2) years |
Responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production. | 04/16/2021 |
| 8990 | Ajinomoto Bio Pharma Services San Diego, CA Drug Product Manufacturing Associate I - Formulations Bachelor’s degree in a Life Sciences discipline or equivalent preferred. Exp: Zero to two (0-2) years |
You will work in a GMP clean room environment where you will be responsible for execution of routine production and manufacturing procedures to support processes and ensure compliance with regulatory requirements. | 04/16/2021 |
| 8991 | Ajinomoto Bio Pharma Services San Diego, CA Drug Substance Manufacturing Associate I Bachelor’s degree in a life science discipline or equivalent preferred. Exp: 0-2 years |
Responsible for executing the day to day responsibilities related to the Drug Substance Manufacturing group under the guidance of Aji Bio-Pharma Service’s established procedures and policies. | 04/16/2021 |
| 8992 | Ajinomoto Bio Pharma Services San Diego, CA Microbiology Technician Bachelors degree preferred in a Life Sciences discipline. Exp: Zero to two (0-2) years |
This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. | 04/16/2021 |
| 8993 | Ajinomoto Bio Pharma Services San Diego, CA QC Raw Materials Associate I Bachelor’s degree in a Life Sciences discipline or equivalent preferred. Exp: Zero to two (0-2) years |
Responsible for conducting routine analysis, inspection, testing and release of raw materials and Active Pharmaceutical Ingredients (APIs) under supervision. | 04/16/2021 |
| 8994 | Altimmune Gaithersburg, MD Associate Scientist Master’s degree. Exp: 1+ years |
The Scientist is responsible for conducting in vitro experiments in order to produce reliable and precise data to support the scientific investigation of vaccine immunogenicity and therapeutic efficacy. | 04/16/2021 |
| 8995 | American Regent Columbus, OH QC Microbiologist I Bachelor’s degree in Microbiology, Biology, or equivalent Life Science curriculum required. Exp: One year |
Primarily responsible for performing, coordinating and tracking the microbiological testing for in-process and finished products as well as monitoring of controlled manufacturing facilities and utility systems. | 04/16/2021 |
| 8996 | American Regent Shirley, NY QC Chemist I - 11pm - 7:30 am Bachelor’s degree in Science, Chemistry, Biology or related field required. Exp: one (1) year |
*Please Note: This position will train on the 1st shift for approximately 3 months* This position is centered on testing of raw materials, in-process, and finished product samples accurately and efficiently to determine chemical identity, potency and purity of pharmaceutical products manufactured by American Regent, Inc. | 04/16/2021 |
| 8997 | American Regent Shirley, NY QC Chemist I Bachelor’s degree in Science, Chemistry, Biology or related field required. Exp: One year |
This position is centered on testing of raw materials, in-process, and finished product samples accurately and efficiently to determine chemical identity, potency and purity of pharmaceutical products manufactured by American Regent, Inc. | 04/16/2021 |
| 8998 | Ampac Analytical La Porte, TX Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Exp: Zero (0) to two (2) years |
This position requires utilization of independent judgement to analyze raw materials, in-process, intermediate and final product, stability, and microbiology samples for the pharmaceutical industry, using various validated methodology as well as experimental ones. | 04/16/2021 |
| 8999 | Ampac Analytical Rancho Cordova, CA Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Exp: One (1) to two (2) years |
Must use independent judgment to analyze and make determinations as to the quality of a product, using analytical equipment pertinent to the appropriate application of skills. Use various laboratory procedures related to analysis of bulk and pharmaceutical chemicals. | 04/16/2021 |
| 9000 | Ampac Analytical Rancho Cordova, CA Analytical Scientist Bachelor's degree in Chemistry required. Master's degree in Chemistry preferred. Exp: One (1) to three (3) years |
Candidate will develop and validate methods; provide analytical support to the research and development group to meet project goals; select appropriate methods and techniques in performing experiments; collaborate with analytical personnel to help develop routine analytical methods; work cross functionally to achieve target goals and proactively seek out potential solutions to issues. | 04/16/2021 |
| 9001 | Ampac Analytical Petersburg, VA Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Exp: Zero (0) to two (2) years |
This position requires utilization of independent judgement to analyze raw materials, in-process, intermediate and final product, stability, and microbiology samples for the pharmaceutical industry, using various validated methodology as well as experimental ones. | 04/16/2021 |
| 9002 | Ampac Analytical Petersburg, VA Analytical Scientist Bachelor's degree in Chemistry required. Master's degree in Chemistry preferred. Exp: One (1) to three (3) years |
Candidate will develop and validate methods; provide analytical support to the research and development group to meet project goals; select appropriate methods and techniques in performing experiments; collaborate with analytical personnel to help develop routine analytical methods; work cross functionally to achieve target goals and proactively seek out potential solutions to issues. | 04/16/2021 |
| 9003 | Ampac Analytical Petersburg, VA Analytical Scientist Bachelor's degree in Chemistry required. Master's degree in Chemistry preferred. Exp: One (1) to three (3) years |
Candidate will develop and validate methods; provide analytical support to the research and development group to meet project goals; select appropriate methods and techniques in performing experiments; collaborate with analytical personnel to help develop routine analytical methods; work cross functionally to achieve target goals and proactively seek out potential solutions to issues. | 04/16/2021 |
| 9004 | Angion Biomedica Uniondale, NY Research Associate Bachelor’s degree Biology, Biochemistry, Cell Biology, or Immunology. Master's Degree Biology, Chemistry, Biochemistry preferred. Exp: 1 - 2 years |
Prepares data presentation and analysis as well as laboratory cleaning and organization Assists with manuscripts and grant applications submissions Under supervision, performs chemical, biological, immunologic, and microscopic assays | 04/16/2021 |
| 9005 | ANGLE Biosciences Toronto, CA Research Associate BSc. in Life Sciences, preferably in a field of oncology, molecular biology or cell biology. Exp: 1-3 years |
We are currently recruiting for a Research Associate to work in our regulated lab environment designing, performing, and reporting laboratory experimental tasks for the development, optimization, verification, and validation of assays to analyze nucleic acids or protein expression in human clinical samples. | 04/16/2021 |
| 9006 | Apic Bio Cambridge, MA Research Associate - Analytical Development BS/MS degree in Biology, Chemistry, Chemical Engineering or related fields. Exp: 0-2 years |
Apic Bio is seeking a highly motivated and organized Research Associate to join the Analytical Development Group. The qualified candidate will establish and execute various analytical methods for AAV (to include PCR, DLS, CGE, ELISA, cell-based assays, etc.). | 04/16/2021 |
| 9007 | Apic Bio Cambridge, MA Research Associate - In vivo BS in life sciences. Exp: 1 year |
Apic Bio is seeking a highly motivated Research Associate to join the Preclinical Group with a focus on translational gene therapy. Primary responsibilities will be to support in vivo studies in mice with a focus on respiratory physiology. | 04/16/2021 |
| 9008 | BilionToOne West Menlo Park, CA Research Associate - Bioinformatics BS or MS in Molecular Biology, Bioengineering, Bioinformatics, Computational Biology, Physics or related field. Exp: 1-2 years |
Currently looking for a Research Associate with a computational/bioinformatics focus to join our Clinical Operations team. Under the guidance and supervision of the Director of Process Engineering, this person will learn and develop bioinformatics pipelines for analysis of next-generation DNA sequencing data. | 04/16/2021 |
| 9009 | BilionToOne West Menlo Park, CA Research Associate BS or MS in Molecular and Cell Biology, Microbiology, Biophysics, Biochemistry, or related field. Exp: 1-2 years |
Currently seeking a research associate to join our interdisciplinary and innovative R&D team and help us develop novel molecular diagnostics. This person will be responsible for helping to design and performing the molecular assays and experiments under the supervision of our senior research team. | 04/16/2021 |
| 9010 | BilionToOne West Menlo Park, CA Clinical Laboratory Scientist (CLS) Bachelor's degree in the chemical, physical or biological sciences, plus a current California Clinical Laboratory Scientist License. Exp: 1-2 years |
We are looking for a driven Clinical Laboratory Scientist (with California Clinical Laboratory Scientist License) to perform UNITY, the only non-invasive prenatal test (NIPT) that can detect inherited disorders such as sickle cell disease, spinal muscular atrophy, and cystic fibrosis in the baby directly from maternal blood. | 04/16/2021 |
| 9011 | Arcturus Therapeutics San Diego, CA Research Associate I, Process Development, Technical Operations MS/BS degree in biochemistry, biological sciences, pharmaceutical sciences, chemistry, chemical engineering, molecular biology, or other relevant dis Exp: 1 to 5 years |
The Research Associate II performs a variety of well-defined support functions and participates in some independent research activities, as outlined by their supervisor. Especially, this position requires a qualified professional experience in planning, executing, and documenting the risk assessment and process characterization of manufacturing unit operations. | 04/16/2021 |
| 9012 | Arrakis Therapeutics Waltham, MA Research Associate, Compound Management B.S. in Chemistry, Biology, Biochemistry, Biotechnology, or Biomedical Engineering. Exp: 1-2+ years’ |
Provide daily support to Arrakis scientists across many departments, using state-of-the-art laboratory automation equipment and software to prepare compound plates in a wide variety of formats. The role also involves working closely with Medicinal Chemists to routinely procure new compounds from multiple vendors. | 04/16/2021 |
| 9013 | Arrowhead Pharmaceuticals San Diego, CA Associate Scientist, Histology Bachelor’s in Cell Biology, Molecular Biology, Biochemistry or a related discipline. Exp: 1 year |
The Sr. Research Associate/Associate Scientist is a member of the Histotechnology team in the Toxicology Department. The Histotechnology team supports the Company’s preclinical drug development efforts by designing studies, collecting, preparing and analyzing samples generated by the Company’s animal studies. | 04/16/2021 |
| 9014 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, Bioconjugation BS or MS Chemistry or Biochemistry degree with excellent understanding of organic and analytical chemistry. Exp: Entry Level |
Seeking an Associate Scientist to join the Chemistry Department. The successful candidate will primarily focus on bioconjugation, analytical chemistry, formulation, and some small molecule organic synthesis. S/He will be joining a team of highly motivated and experienced scientists, and will contribute to the success of Arrowhead programs. | 04/16/2021 |
| 9015 | Arrowhead Pharmaceuticals Madison, WI Analytical Development Scientist B.S in Chemistry (or related field). Exp: 1-5 years, Entry Level |
The position is in the Analytical Development (AD) Group within the CMC Manufacturing Organization. An AD Scientist will support method development/validation activities for new drug substances and drug product. He/She will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies. | 04/16/2021 |
| 9016 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, CMC Process Development BS/BA in Chemistry or related field. Exp: 1 year |
We have an immediate opening for an Associate Chemist to work as a Chemist in the Chemistry, Manufacturing, and Controls Group focusing on small molecule process development. This is an ideal position for an individual with an organic chemistry background who has an interest in projects related to novel technology in synthesis and purification of small molecules and bioconjugates. | 04/16/2021 |
| 9017 | Arrowhead Pharmaceuticals Madison, WI Associate Production Chemist Bachelors degree in a scientific field. Exp: Entry level to 5 years |
We have an immediate opening for an Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. | 04/16/2021 |
| 9018 | Arrowhead Pharmaceuticals Madison, WI Associate Production Chemist (2nd Shift) Bachelors degree in a scientific field. Exp: Entry level to 5 years |
We have an immediate opening for a 2nd Shift Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. | 04/16/2021 |
| 9019 | Ginkgo Bioworks Boston, MA Research Associate, Protein Purification BS/MS in Molecular Biology, Biochemistry, Bioengineering, Chemical Engineering, Biophysics, or Related Exp: 0+ Years |
As a Research Associate, you will perform small scale protein purifications, as well as make use of Ginkgo Bioworks' high-throughput purification platform. Multiple opportunities are available to learn exciting instrumentation such as FPLC systems and liquid handlers. You will also interact closely with several teams including fermentation, high-throughput screening (HTS) and protein engineering. Not only will you expand your scientific skillset, but also your scientific communication as you will present research findings across multiple program teams and interface directly with customers about key deliverables. | 4/19/2021 |
| 9020 | Glaukos San Clemente, CA Clinical Data Manager BS in Biological Science, Nursing, or Other Relevant Discipline Exp: 0+ Years |
The Clinical Data Manager, based in San Clemente, CA, eventually based in Aliso Viejo, CA is responsible for study Data Management activities from study start up to close out. Providing input into the data cleaning strategy and aiding data cleaning efforts supporting Clinical Studies. This individual must possess good project management and analytical skills and have the ability to review data using various reporting and analytics tools.The Clinical Data Manager, based in San Clemente, CA, eventually based in Aliso Viejo, CA is responsible for study Data Management activities from study start up to close out. Providing input into the data cleaning strategy and aiding data cleaning efforts supporting Clinical Studies. This individual must possess good project management and analytical skills and have the ability to review data using various reporting and analytics tools. | 4/19/2021 |
| 9021 | Glaukos San Clemente, CA Manufacturing Technician II - Pharma BS in Science or Engineering Exp: 0-2 Years |
Responsibilities: Prepare components and build assemblies. Prepare bulk drug formulations. Perform filing, capping, and crimping operations. Perform packaging and labeling operations. Perform sampling and visual inspections. Perform documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR). Perform and/or track clean room, environmental chambers, and equipment preventive maintenance (PMs). | 4/19/2021 |
| 9022 | Globus Medical Methuen, MA Mechanical Engineer BS in Relevant Discipline Exp: 1-5 Years |
The Mechanical Engineer will work to develop medical robots by working with top surgeons and a cross-functional engineering team. The candidate will be responsible for tracking robot end effectors and other surgical apparatus in the operating room as well as developing cutting edge sensors, displays and techniques. The ideal candidate should demonstrate strong mechanical design skills and be comfortable working with individuals across several engineering disciplines. This is a highly creative team working on novel technologies, so intellectual curiosity and a willingness to learn and adapt to new things are a must. | 4/19/2021 |
| 9023 | Globus Medical Audobon, PA Research Engineer MS in Science or Engineering Exp: 1-2 Years |
The Research Engineer will be responsible for planning, coordination, successful execution, and publication of various research projects for spine surgeons, residents, and product development. In addition, this position will function in a cross-disciplinary environment and must have experience or be willing to be trained in image analysis, micro-CT, biomechanical principles, and orthopedic basic sciences. The Research Engineer must have strong self-starting qualities to independently manage coordination of multiple projects to ensure timely and successful completion. | 4/19/2021 |
| 9024 | Gore Medical Elkton , MD Quality Control Laboratory Technician BS in Biology, Chemistry, or Related Exp: 0+ Years |
Gore is looking for an East Coast Testing Center Analytical Laboratory Technician to join a team that supports medical device manufacturing by providing quality control (QC) analytical and biological laboratory testing services in Elkton, Maryland. This is a hands-on role in a regulated environment requiring quick turnaround times while executing high quality work. The primary responsibility is to perform routine QC testing at the East Coast Testing Center (ECTC). | 4/19/2021 |
| 9025 | Gore Medical Elkton , MD Quality Control Lab Associate BS in Science or Engineering Exp: 0+ Years |
The Lovett Quality Control lab team is looking for an energetic, flexible, organized, and high performing QC lab associate in Elkton, Maryland. This associate will have primary responsibility of routine testing for product release and process monitoring in the QC lab as well as support projects that partner with new product development and engineering associates to develop and optimize new test methods. | 4/19/2021 |
| 9026 | Gossamer Bio San Diego, CA Clinical Document Management Associate BS in Relevant Scientific Discipline Exp: 1+ Years |
Clinical Document Management Associate (CDMA), Clinical Operations, is responsible for supporting document management across clinical study team(s) to support operational execution and delivery of quality studies and quality processes according to protocols, SOPs, and Gossamer policies and procedures, applicable regulations and principles of GCP. The CDMA will prioritize and handle multiple tasks effectively in a fast-paced Research and Development (R&D) environment. Under the guidance of Clinical Operations management, the individual will coordinate, track, and manage daily document processing activities for multiple clinical studies to support both the internal project team(s) and the CRO(s). | 4/19/2021 |
| 9027 | Gossamer Bio San Diego, CA Associate, Quality Assurance BS in Relevant Scientific Discipline Exp: 0-2+ Years |
The Associate / Sr. Associate Quality Assurance will support the company’s quality and regulatory systems in compliance with industry best practices. The Associate will implement and maintain corporate and departmental procedures. This position will additionally serve as an integral member representing quality on cross functional teams. | 4/19/2021 |
| 9028 | Grand River Aseptic Manufacturing Grand Rapids, MI Microbiology Technician BS in Microbiology or Related Exp: 0-2 Years |
Responsibilities: Performs sampling of water pure steam to support manufacturing activities. Performs Environmental Monitoring of aseptic filling rooms and supporting areas. Performs bioburden testing of water an in-process samples to detect microorganisms and to obtain information on types and levels of microbial contamination. Performs Total Organic Carbon and Conductivity testing on water. Maintains laboratory equipment - cleaning and calibration. | 4/19/2021 |
| 9029 | Grand River Aseptic Manufacturing Grand Rapids, MI Facilities Engineer BS in Engineering, Science, or Technical Discipline Exp: 1+ Years |
Job Summary: Assist the Engineering and Operations departments by specializing in facility and utility optimization and providing subject matter expertise (SME) on mechanical systems. Provide logistics lead projects. Oversee construction activities demonstrating, building, and enforcing the best practices for all engineering projects and functions within the facility. Work independently on multiple high-profile tasks simultaneously to ensure maximum uptime of the facility. Work closely with maintenance staff to help coordinate inspections and repairs, as well as the testing and calibration of all instrumentation, electrical, and mechanical systems. Aid the Engineering Manager in day-to-day facilities administration. | 4/19/2021 |
| 9030 | Grand River Aseptic Manufacturing Grand Rapids, MI QA Specialist BS in Life Science or Relevant Discipline Exp: 1-2 Years |
Job summary: Support the quality systems as they relate to the manufacturing and testing of cGMP drug products. Provide quality oversight for terminal sterilization, visual inspection, labeling and packaging Operations of parenteral drugs. Perform the quality release of incoming materials. Review documentation and quality records. | 4/19/2021 |
| 9031 | Grand River Aseptic Manufacturing Grand Rapids, MI QA Technician Batch Record Review BS in Life Science or Relevant Discipline Exp: 1-2 Years |
Job Summary: Support the quality systems as they relate to the manufacturing and testing of cGMP drug products, including the review of documentation and quality records associated with filling, terminal sterilization, visual inspection, labeling and packaging. | 4/19/2021 |
| 9032 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Lab Technician BS in Biochemistry, Biotechnology, or Related Exp: 0+ Years |
Support quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to providing general laboratory support for raw material, stability and finished product testing, as well as QA support in AQL inspection and batch release. | 4/19/2021 |
| 9033 | Grand River Aseptic Manufacturing Grand Rapids, MI Aseptic Manufacturing Associate BS in Relevant Scientific Discipline Exp: 0-1 Years |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. | 4/19/2021 |
| 9034 | GreenLight Biosciences Medford, MA Research Associate Molecular Biology MS in Molecular Biology, Biological Engineering, Biochemistry, or Related Exp: 1+ Years |
Responsibilities: Support the development of new RNA-based vectors by execution and analysis of different experiments according to SOPs. Perform biochemical and cell-based assays to evaluate RNA specific activity and expression of antigens and antibodies. Support routine RNA sample production efforts for internal and external collaborations, as necessary. Perform standard molecular biology experiments (including plasmid design & cloning, DNA amplification, DNA & RNA gel electrophoresis, etc.) | 4/19/2021 |
| 9035 | GreenLight Biosciences Medford, MA Research Associate - Bioassay BS/MS in Biology, Biochemistry, or Equivalent Exp: 0-2 Years |
The successful candidate will work closely with a diverse R&D team to achieve company goals and help advance the company’s RNA platform technology. | 4/19/2021 |
| 9036 | GreenLight Biosciences Medford, MA Research Associate Analytical Sciences BS/MS in Chemistry, Biochemistry, or Equivalent Exp: 0-4 Years |
As a valued team member, the Research Associate will perform a range of bioanalytical assays to quantify and characterize raw materials such as plasmid DNA, mRNA products, and intermediates of the production process. This role allows learning of new methodologies and cutting-edge science, exposure to molecular biology and characterization techniques. The Research Associate will implement the testing with high accuracy and commitment to quality to produce highly reliable results instrumental in R&D discovery and mid- to late phase product development within a highly collaborative team. | 4/19/2021 |
| 9037 | GreenLight Biosciences Medford, MA Research Associate, Immunology BS in Biological Science or Related Exp: 0-2 Years |
This is an Entry Level position, ideal for recent graduates and early career stage researchers looking to work in a start-up environment. The candidate will work collaboratively with internal and external teams to help advance the Human Health discovery and clinical pipeline. Research activities will involve all stages of the vaccine discovery pathway from antigen discovery, characterization, and evaluation in vitro and in vivo to the validation of clinical samples from human trials. Applicants should be outstanding at lab-based research, collaborative team members, excellent communicators with a passion for learning, innovation and improving human health. | 4/19/2021 |
| 9038 | GreenLight Biosciences Research Triangle Park, NC Research Associate, Fungal BS in Microbiology, Biology, Molecular Biology, or Related Exp: 1-2 Years |
GreenLight Biosciences is seeking an exceptional, highly motivated Research Associate to work on projects that utilize cutting edge RNA technologies to develop novel biopesticides. The successful candidate will support research in fungal plant pathology. The ideal candidate will have basic microbiology knowledge, excellent sterile technique, and experience with common laboratory tasks, such as media prep, assay plating, culture maintenance, and general plant pathology. The successful candidate will support research in fungal assay development of controlled environment and greenhouse studies. Strong technical, organizational, and communication skills, as well as a commitment to excellence and high-quality work, are essential. | 4/19/2021 |
| 9039 | IQVIA Valencia, CA Clinical Lab Scientist 1- Chemistry BS in Relevant Discipline Exp: 0-5 Years |
Provides professional and technical skills and knowledge to ensure accurate and timely performance of regular and specialized testing in or more areas of clinical laboratory such as Hematology, Molecular, Microbiology, Auto Chemistry, Special Chemistry, Immunology, and Flow Cytometry to obtain data for use in diagnosis and recording clinical trial laboratory test results. Performs work in accordance with ICH E6 Guideline for Good Clinical Practice. | 4/5/2021 |
| 9040 | IQVIA Ithica , NY Associate Scientist, LCMS BS in Chemistry or Biology Exp: 1+ Years |
The Associate Scientist Core LC/MS (Liquid Chromatography/Mass Spectrometry) employs liquid chromatographic separation techniques and mass spectrometric analysis for data collection. This is an entry level analyst position that will work under the tutelage of higher-level analysts in the Core LCMS lab. In addition to instrument operation, the Associate Scientist may with some initial supervision perform basic instrument maintenance. The analyst is responsible for documentation in accordance with SOPs and regulations, and data processing in a manner which meets company quality best practices, objectives and timelines. | 4/5/2021 |
| 9041 | IQVIA Durham, NC Lab Data Analyst BS in Clinical, Biological, or Computer Sciences, or Related Exp: 1+ Years |
This involves capturing data delivery requirements, formatting of custom delivery files, verification of regulated study data, supporting multiple delivery methods and aiding in the development of custom formatting software, if applicable, and consistent compliance with established systems and workflows. Able to work within regulatory constraints and comfortable with a high degree of uncertainty, rapid timelines, balancing multiple projects of both short and long-term outcomes. High level of attention to detail, comfortable in a client-facing role not necessarily and proactive at gathering information across teams, troubleshooting and resilience, and ability to adapt to shifting priorities a must. | 4/5/2021 |
| 9042 | IQVIA Durham, NC Lab Tech Specialist (Metrologist) - BioA BS in Life Science Discipline Exp: 1+ Years |
Provides input into Global Laboratory Harmonization and reviews local laboratory requirements for new studies, responds to technical inquiries and provides technical documents and data either directly or by maintaining study specific databases. Monitors the local Technical Support Helpdesk, responding to inquiries from other departments and clients requesting specific laboratory information. Develops and maintains the local laboratory Quality Control Program and database, performs statistical analysis of data and quality control performance data reviews and purchases and distributes quality control materials in accordance with Global Lab Harmonization policy and regulatory guidelines. | 4/5/2021 |
| 9043 | IQVIA Ithica , NY Medical Writer 1 BS in Life Science Discipline Exp: 1-2 Years |
Prepares or contributes to the preparation of pharmacokinetic (PK) method validation and bioanalytical sample analysis reports for either internal Q² Solutions customers or external clients under the guidance of senior staff. May also prepare other technical documents and deliverables. Participates in project teams and may lead specific tasks, consulting senior staff as necessary. | 4/7/2021 |
| 9044 | IQVIA Ithica , NY Associate Scientist, Sample Preparatiion - LCMS Biologics BS in Life Science Discipline Exp: 0+ Years |
Performs a wide variety of increasingly complex technical laboratory experiments and procedures related to sample preparation. This can include method development/optimization and troubleshooting experiments, validation, and study sample preparation in addition to the preparation of solutions and reagents. Assists in maintaining lab equipment, supports lab safety, and complies with IQVIA procedures and Good Laboratory Practice (GLP) requirements, as applicable.Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice | 4/7/2021 |
| 9045 | IQVIA Atlanta or Remote, GA Scientific Writer - Bioanalytical BS/MS in Life Science Discipline Exp: 1-3 Years |
Acts as a Lead Medical Writer on straightforward projects (e.g. simpler documents under standard timelines). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Negotiates timelines and discusses/resolves customer comments, with senior support as needed. Keeps abreast of current medical and/or technical writing/regulatory knowledge, including GCP, along with developments and advances in drug development/medical and/or technical writing. | 4/7/2021 |
| 9046 | Genalyte San Diego, CA Process Development Associate I BS in Chemistry or Biological Sciences Exp: 0-2 Years |
Under direct supervicion, this position is responsible for assisting manufactuing and team members in carrying out process development, technology transfer, quality control, manufacturing processes and tasks involving a variety of laboratory methods, equipment, and procedures. | 4/7/2021 |
| 9047 | Genalyte San Diego, CA Research Associate II BS in Biochemistry, Chemistry, Molecular Biology, or Related Exp: 1-2 Years |
Responsibilities: Prepare reagents for use in the lab following SOPs, perform key procedures and experiments, develop and update SOPs, analyze data from various sources, document experiments in lab notebook, perform experiments that will be submitted to the FDA for 510(k). | 4/7/2021 |
| 9048 | GenapSys Redwood City, CA Research Associate, Molecular Biology BS in Molecular Biology, Biochemistry, Chemistry, or Bioengineering Exp: 1-2 Years |
As GenapSys’ new Research Associate you will be a key member of their enzyme engineering and production effort. Some key areas of impact you will have in the first year include expression, purification, and characterization of polymerase and recombinase enzymes. You will report to a Principal Scientist. | 4/7/2021 |
| 9049 | GenapSys Redwood City, CA Research Associate, Chemistry BS/MS in Organic Synthesis, Polymer or Surface Chemistry, Materials Science, Chemical Engineering, or Related Exp: 0+ Years |
Responsibilities: Carry out routine synthesis, purification and bioconjugation, deliver completed experiments in-line with production schedules. Perform in-house QC testing of polymers and bio-conjugated material using absorbance readers and gel electrophoresis. Assist in scale-up and optimization of new processes for smooth transfer from R&D to technical manufacturing operations. Collaborate with team members to integrate findings and advancements into current laboratory SOPs. | 4/7/2021 |
| 9050 | Genetech San Francisco, CA Scientific Researcher, High-Throughput 293 Protein Expression and Purification BS/MS in Biology, Biochemistry, or Related Exp: 1+ Years |
He/she will help evaluate protein expression constructs and expression levels for a wide variety of proteins of therapeutic interest in support of basic research, small and large molecule drug discovery. He/she will support automation-driven protein construct screening in a core facility setting to enable large-scale protein production and work with stakeholders to optimize expression levels and quality of proteins. The successful candidate will be responsible for performing protein expression, small scale purification and characterization of proteins (affinity purification, SDS-PAGE, Western analysis) produced using E. coli, baculovirus, and mammalian transient systems. | 4/9/2021 |
| 9051 | Genetech San Francisco, CA Senior Administrative Assistant, Infectious Diseases BS in Relevant Discipline Exp: 0+ Years |
The successful candidate will be adept at problem solving and will anticipate, determine, and fulfill Vice President and staff needs in a proactive manner. They will have excellent interpersonal and communication skills and experience in multi-tasking, prioritization, organization, problem-solving, and working independently. The candidate will display excellent judgment and discretion regarding sensitive/confidential and proprietary information and be comfortable learning new technologies or software applications to manage staff needs. The candidate will contribute to organizational and corporate goals to ensure the smooth daily operation of the department. | 4/9/2021 |
| 9052 | Genetech San Francisco, CA Manufacturing Technicican - Bioprocess BS in Life Sciences or Engineering Exp: 1+ Years |
The Manufacturing Technician will be responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, formulation, freeze thaw and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). | 4/9/2021 |
| 9053 | Genetech Hillsboro, OR QC Analyst I BS in Relevant Scientific Discipline Exp: 0+ Years |
Responsibilities include sampling and testing of utility systems (Color, Appearance, Odor, TOC, Conductivity, Bioburden, Endotoxin, Particulates and Moisture), facility monitoring (viable monitoring plates and non-viable particulate), data trending and report generation. Other responsibilities include in-process samples and compendial final product testing, chemical and microbiological analysis of cleaning changeover samples, testing of biological indicators and media fill readout. The candidate will share maintenance responsibilities with other laboratory personnel such as reagent preparation, media growth promotion, and cleaning of incubators and biosafety cabinets. | 4/9/2021 |
| 9054 | Genetech Oceanside, CA Bioprocess Manufacturing Technician BS in Life Sciences or Engineering Exp: 0+ Years |
As a Bioprocess Manufacturing Technician, you will be responsible for producing medicine in a highly automated and controlled environment. Each product has a specific recipe; you will follow this recipe, along with the standard operating procedures, to operate the production equipment across various areas, including raw material dispensing/aliquoting, cell culture and purification. You will maintain records and follow all the steps necessary to comply with regulatory requirements within a current Good Manufacturing Practices (cGMP) environment. | 4/9/2021 |
| 9055 | Genetech San Francisco, CA Pilot Plant Master Technician/Associate Technical Specialist BS in Life Science Discipline Exp: 0-1+ Years |
The team member’s core responsibilities will encompass all the activities involved in carrying out day-to-day Process Development experiments with bacterial and CHO culture processes, ranging from 15mL to 1000L vessels. This will include cleaning, sterilization, batching, and inoculation of bioreactors; preparing media and solutions, performing cell counts, operating harvest equipment, equipment troubleshooting, and recording and collecting experiment data. The successful candidate will operate computers and Human Machine Interfaces for process control and data entry. He/she will collaborate with other shift personnel and staff to carry out and coordinate experiments. The candidate will be knowledgeable of all standard operating procedures and have the ability to update and implement new procedures and provide suggestions for process improvement. | 4/9/2021 |
| 9056 | Genetech San Francisco, CA Research Associate/Assistant MS in Chemical Engineering, Biochemical Engineering, Biochemistry, or Equivalent Exp: 0-2 Years |
Within the Purification department this team member will develop, characterize, validate and implement recombinant protein and novel therapeutic purification processes from laboratory to manufacturing scale. This individual will interact with engineers and scientists within the Pharma Technical Development organization as well as collaborate with members from Manufacturing, Quality, and Regulatory. | 4/9/2021 |
| 9057 | Genedata Lexington, MA Biopharma Enterprise Solutions Engineer BS in Computer Science, Life Science, Engineering, or Related Exp: 1-2 Years |
The Biopharma Enterprise Solution Developer for the Biologics business unit supports the installation life cycle of the Genedata Biopharma Platform at customer sites in the US and in the cloud. The primary role is the development of configurations and external solutions to assist with the roll-out of our core product at customer sites. This position is also responsible for installing, maintaining, and updating the Genedata Biopharma Platform and contributing to technical, quality, and process documentation. | 4/9/2021 |
| 9058 | GeneDx Gaithersburg, MD DNA Sequencing Lab Technician I BS in Medical Technology or Related Life Science Exp: 0-1 Years |
Responsibilities: Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. | 4/9/2021 |
| 9059 | GeneDx Gaithersburg, MD Quality Systems Specialist - Data Science BS in Relevant Scientific Discipline Exp: 1-3 Years |
Responsibilities: Implements Quality Systems programs that are consistent with company policies and regulatory standards. Audits and reviews quality data according to established procedures. Maintains tools for monitoring compliance training, corrective actions, audits, and document control. Supports corrective action task force initiatives. | 4/9/2021 |
| 9060 | GeneDx Gaithersburg, MD Lab Applications Specialist - Informatics BS in Computer Science, Biology, Software Engineering, or Related Exp: 0+ Years |
The Laboratory Applications Specialist is responsible for working with GeneDx lab teams to configure and support LIMS applications for workflow and lab processes. They will be responsible for gathering and analyzing user requirements, configuring workflows and improving existing workflows via configuration. This position will work within the Informatics group and with the LIMS Administrator to be responsible for the performance, configuration, troubleshooting, training, and other related issues with LIMS applications. | 4/9/2021 |
| 9061 | GeneDx Gaithersburg, MD Equipment Coordinator - Facilities BS in Relevant Scientific Discipline Exp: 1-3 Years |
The Equipment Coordinator will join the Facilities team with particular responsibilities directed at specific equipment calibration events. Ex. Driftcon Thermocycler Testing, Semi Annual Pipette Calibrations & Annual Functional Testing, etc. Along with their equipment responsibilities they will be assisting with updating and maintaining the current GeneDx equipment policies and any other QS related items. They will also assist with monitoring and maintaining all lab equipment and their respective support systems in all laboratory sections. | 4/9/2021 |
| 9062 | GeneDx Gaithersburg, MD DNA Extraction Technician BS in Medical Technology or Related Life Science Exp: 0-1 Years |
Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. | 4/9/2021 |
| 9063 | GeneDx Gaithersburg, MD Lab Technician, Microarray BS in Medical Technology, Chemistry, Biology, or Related Exp: 0+ Years |
The Medical Laboratory Technician or Technologist will perform all necessary laboratory testing in the detection, diagnosis, and prognosis of disease. The Medical Laboratory Technician or Technologist will work collaboratively with the laboratory team to provide testing services to the clients. Additional tasks can be assigned at the discretion of the Supervisor/Manager/Director. | 4/9/2021 |
| 9064 | GeneDx Gaithersburg, MD Quality Systems - Document Control & Retention BS in Relevant Scientific Discipline Exp: 1-3 Years |
Responsibilities: Implements Quality Systems programs that are consistent with company policies and regulatory standards. Implements and manages the record retention program. Manages the document control system - ensuring timely review and document completeness. Maintains tools for monitoring compliance training, corrective actions, audits, and document control. | 4/9/2021 |
| 9065 | GenMarkDx Carlsbad , CA Research Associate II, PTS MS in Biochemistry, Molecular Biology, or Related Exp: 0-2 Years |
You will execute a range of molecular biology procedures, reagent preparation, data analysis, and laboratory duties under minimal supervision. You will work closely with cross functional teams to investigate root cause of anomalies reported during Quality Control or from Customer Technical Support. | 4/9/2021 |
| 9066 | GenMarkDx Carlsbad , CA Research Associate I BS in Chemistry, Biochemistry, Molecular Biology, or Related Exp: 1+ Years |
You will execute a range of molecular biology procedures, reagent preparation, and bioanalytical procedures and laboratory duties under supervision. Performing lab duties while maintaining associated health and safety guidelines while maintaining inventory of laboratory reagents and supplies. | 4/9/2021 |
| 9067 | GenMarkDx Carlsbad , CA Electrical Engineer I BS in Engineering Discipline Exp: 1-2 Years |
This new exciting role at GenMark will work under supervision from senior contributors, serve as an electrical engineer in sustaining engineering and concept-to-market efforts for IVD instrumentation. Apply hands-on involvement in on-market support for existing and new products, troubleshooting and root cause analysis, creation and maintenance of input and output specifications, concept and feasibility activities, prototyping, testing, and transfer to manufacturing. | 4/9/2021 |
| 9068 | GenMarkDx Carlsbad , CA Quality Control Specialist I BS in Life Sciences or Engineering Exp: 0-3 Years |
This position conducts incoming, in-process and final release QC testing in a controlled manufacturing environment. This position may also execute validation studies, execute test protocols, analyze data, generate analytical reports, investigate Non-Conformance's, evaluate processes & procedures, utilize statistical techniques, review specifications, and inspect & test equipment. May conduct training on quality related tools, methods, and procedures. Interfaces with R&D, Manufacturing, Quality, and Supply Chain within the company and when appropriate with customers and suppliers on quality related issues. | 4/9/2021 |
| 9069 | Genomatica San Diego, CA Associate Process Chemist I BS in Chemistry, Biochemistry, Chemical Engineering, or Related Exp: 0+ Years |
This position will be responsible for executing lab and pilot-scale experiments that contribute to the development of novel processes for the production of chemicals via fermentation. Technical areas of responsibility span fermentation and downstream separation steps such as filtration, centrifugation, chromatography, extraction, and distillation. He/she will assist in experimental planning, independently set-up, operate, clean and maintain equipment at the bench and pilot scale; collect experimental samples, perform sample assays, perform data analysis and reporting, and maintain/order lab supplies. | 4/9/2021 |
| 9070 | Genomatica San Diego, CA Assocaite Automation Engineer MS in Engineering, Microbiology, Biochemistry, Molecular Biology, or Related Exp: 1-3 Years |
This position plays an integral role in Genomatica's HTP screening and enzyme and strain development teams and will work with other multi-disciplinary scientists and engineers to optimize microbial hosts for diverse bio-based processes. The successful candidate will have demonstrated capabilities of building and operating automated process for enzyme screening or microbial strain development using standard or custom automation platforms. Having abilities of scientific creativity and critical thinking will be crucial to developing innovative solutions in this team environment. | 4/9/2021 |
| 9071 | Genomatica San Diego, CA Research Associate I - QSS BS in Engineering, Microbiology, Biochemistry, Molecular Biology, or Related Exp: 0-3 Years |
This position plays an integral role in Genomatica's strain and fermentation process development, working together with other multi-disciplinary scientists and engineers to optimize microbial hosts in diverse bio-based processes. The successful candidate will have demonstrated capabilities of conceiving innovative experimental design and executing small scale well-plate based experiments with moderate supervision. Having abilities of scientific creativity and critical thinking is crucial to develop innovative solutions in a team environment. | 4/9/2021 |
| 9072 | Genomatica San Diego, CA Process Development Associate I/II BS in Chemistry, Biochemistry, Chemical Engineering, or Related Exp: 0+ Years |
This position will be responsible for executing lab and pilot-scale experiments that contribute to the development of novel processes for the production of chemicals via fermentation. Technical areas of responsibility span fermentation and downstream separation steps such as filtration, centrifugation, chromatography, extraction, and distillation. He/she will assist in experimental planning, independently set-up, operate, clean and maintain equipment at the bench and pilot scale; collect experimental samples, perform sample assays, perform data analysis and reporting, and maintain/order lab supplies. | 4/9/2021 |
| 9073 | Genomatica San Diego, CA Fermentation Associate I/II BS in Chemical/Biochemical Engineering, Bioengineering, Molecular Biology, Microbiology, or Biochemistry Exp: 1-4 Years |
This role works on fermentations of microbial strains engineered for production of industrial chemicals. The bulk of this work is carried out in bench-scale bioreactors. This position will interface closely with the Fermentation engineers and scientists in the Fermentation Science Group to produce conclusive fermentation results that will guide process optimization and scale-up efforts. | 4/9/2021 |
| 9074 | GenScript Piscataway, NJ Production Supervisor, Gene Synthesis MS in Molecular Biology or Related Exp: 1+ Years |
The production supervisor is responsible for training, monitoring and supervising gene synthesis production staff. Responsible for employee assignments, safety, quality, production rates, production reports and timelines. This production supervisor position requires a solid understanding of gene synthesis process in biopharma environment. | 4/9/2021 |
| 9075 | GenScript Piscataway, NJ Sr. Scientist, Process Development & Automation MS in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Biochemistry, Microbiology, or Related Exp: 1-2 Years |
Responsibilities: Lead a project to develop plasmid prep production process and to optimize the procedure and maximize the work efficiency. Work with automation engineers and vendors developing automated plasmid prep automation line. Work with QA group to optimize the consistency of production from batch to batch. Lead other laboratory procedure improvement projects. Ensure compliance with the correct procedures, policies, and health and safety regulations. | 4/9/2021 |
| 9076 | GigaGen San Francisco, CA Research Associate - Tissue Culture BS in Scientific Discipline Exp: 1+ Years |
GigaGen is looking for a research associate to support the expression of antibodies and antibody derivatives for early in vitro testing, in vivo efficacy studies, and tech transfer runs for development. This will include cell line development and cell culture optimization, plus bioreactor production. This position will offer exposure to drug development and manufacturing, with ample opportunity to learn new methods, design your own experiments, and present your work. | 4/9/2021 |
| 9077 | GigaGen San Francisco, CA Research Associate - Protein Purification BS in Scientific Discipline Exp: 1+ Years |
GigaGen is looking for a research associate to support the expression of antibodies and antibody derivatives for early in vitro testing, in vivo efficacy studies, and tech transfer runs for development. This will include both routine protein purification and polishing tasks, as well as frequent process development for novel proteins. This position will span both research and development work, with ample opportunity to learn new methods, design your own experiments, and present your work. | 4/9/2021 |
| 9078 | Ginkgo Bioworks Boston, MA Test Engineer, Analytical Chemist BS/MS in Chemistry, Analytical Chemistry, Chemical Engineering, or Equivalent Exp: 0+ Years |
Responsibilities: Operate and improve processes for strain analysis. Equipment troubleshooting and maintenance. Apply DOE approaches to refine and improve sample extraction and assay methods. Develop processes for verification and quality control of assays to ensure low CV and high reproducibility. Use Ginkgo's Software and Automation infrastructure to execute assays and strain tests. Collaborate with software engineers to ensure that all generated data is captured, stored, and analyzed in Ginkgo's LIMS. | 4/9/2021 |
| 9079 | Varian Austin, TX Microbiology Lab Tech Bachelors Degree in Microbiology or equivalent. Exp: 1-3 years |
The Microbiology Lab Tech will lead the microbiology testing on Varian products in accordance to the Procedures/ Work instructions provided and the corresponding standard. | 4/6/2021 |
| 9080 | Vericel Cambridge, MA QC Analyst I Bachelor’s degree or equivalent education and experience. Exp: 1+ years |
Quality Control (QC) is responsible for incoming inspection of components and raw materials, plus quality testing (e.g. analytical, microbiological) of intermediate, stability and final product samples to demonstrate that all products manufactured meet standards required for cGMP operations. | 04/06/2021 |
| 9081 | Vedanta Biosciences Cambridge, MA Manufacturing Technician BS in a Scientific Discipline or Engineering. Exp: 1 to 3 years |
Looking for a highly skilled biopharmaceutical Manufacturing Technician. The position will be a key element to establish and operate Vedanta’s in-house GMP manufacturing capabilities. | 4/6/2021 |
| 9082 | Vedere Bio Cambridge, MA Research Associate Master’s degree in Biological or related fields. Exp: 0+ year |
Work with the Research Team to support our viral vector production processes and run assays in support of the portfolio of AAV-based programs at Vedere Bio. | 04/06/2021 |
| 9083 | Veracyte San Francisco, CA Clinical Lab Scientist BS/MS degree in Biological Sciences or Medical Technology. With CA CLS license. Exp: 1+ year |
Seeking a new Clinical Laboratory Scientist (CLS) to perform cutting-edge diagnostic testing on patient specimens in our collaborative, high-energy work environment. S/he will accurately perform molecular genetic testing, using a variety of molecular biological techniques including expression microarray analysis. | 04/06/2021 |
| 9084 | Veran Medical Technologies Golden, CO Software Engineer BS degree in Electrical Engineering, Computer Science, Applied Mathematics, or related field required. Graduate degree in related field a plus. Exp: 0-5 years |
Our software engineers focus on developing algorithms and user interfaces to cover a wide range of clinical applications such as Image Guided Surgery, Ultrasound, and Artificial Intelligence. | 04/06/2021 |
| 9085 | Vero Biotech Atlanta, GA QC Chemist Bachelor’s Degree (Chemistry or related field). Exp: 1-3 years |
Performs specifically prescribed tasks of a routine nature to meet company and regulatory quality standards for a combination product (drug/device). Performs testing according to Standard Operating Procedures (SOP’s). | 04/06/2021 |
| 9086 | Verve Therapeutics Cambridge, MA In Vivo Research Associate BS or equivalent in biology or related field. Exp: 1-2 years |
A successful candidate will be self-motivated and technically competent and focused on developing molecular therapies to address genetic risk factors for cardiovascular disease. This individual will be required to plan and perform in vivo studies to advance Verves preclinical research. | 04/06/2021 |
| 9087 | Vivonics Bedford, MA Electromechanical Design Engineer BS in Electromechanical, Electrical, Mechanical, Biomedical Engineering or related field. Exp: 1+ year |
The Electromechanical Design Engineer will work with the Principal Investigator(s) and cross disciplinary R&D team to design and develop the companies’ novel medical and non-medical device solutions. | 04/06/2021 |
| 9088 | Stryker Cary, IL Quality Engineer Bachelor's Degree in Engineering, Science or related field or completion of this degree by June 1, 2021. Exp: 1-2 years |
As the Quality Engineer, you will develop and implement continuous improvement projects and participate in the performance of routine quality system functions. | 04/08/2021 |
| 9089 | Stryker Salt Lake City, UT Quality Engineer BS/MS degree in Engineering or related subject preferred. Exp: 1-3 years |
A Quality Engineer with the ability to drive quality and deliver results. Someone who is an advocate for quality and lean methodologies; a self-directed professional who can identify issues and communicate effectively to all levels within the organization. | 04/08/2021 |
| 9090 | Stryker Arroyo, PR, US Microbiology Laboratory Technician AS/BS preferred degree in in technical or science related field. Exp: 0-2 year’s |
Under general supervision, is responsible for accurate and timely processing of routine laboratory testing and procedures required in the Laboratory. | 04/08/2021 |
| 9091 | Stryker Ft Lauderdale, FL Systems Engineer Bachelor's Degree; Computer Science, Biomedical discipline preferred. Exp: 0+ years’ |
As a Systems Engineer, you will be involved with system level design of best in class orthopedic robotic surgical applications. You will have the ability to work with cross-functional sub-system teams to design software and hardware elements while blending engineer with bio-mechanics of the human body. | 04/08/2021 |
| 9092 | Xencor Monrovia, CA CON - Research Associate A four-year degree is desired but not mandatory. Exp: 6 months- 1 year |
The Research Associate, Discovery Biology and Pharmacology is a temporary role in our Research facilities. Lab experience in Academia or Industry. Experience with primary tissues, cell lines, and mammalian cell culture sterile technique. | 04/08/2021 |
| 9093 | Xencor Monrovia, CA CON - Research Associate 1 BS in Molecular Biology or a related field. Exp: 1+ years |
Join the Molecular Biology group. The successful candidate will have the opportunity to contribute directly to the exciting drug discovery process by implementing the use of standard and innovative molecular cloning technologies for high-throughput construction of recombinant proteins and vector variants. | 04/08/2021 |
| 9094 | XenoTech Kansas City, KS Research Assistant or Scientist I Bachelor’s degree in biological or chemical sciences preferred. Exp: 0 - 1+ year |
The Research Assistant assists with routine laboratory functions including diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintains inventory of supplies, and various other responsibilities. | 04/08/2021 |
| 9095 | Xeris Pharmaceuticals Chicago, IL Analytical Research Associate BS or MS degree in biology, biochemistry, chemistry or related discipline. Exp: 0-2 years |
Assists in the execution of analytical and characterization methods to support pharmaceutical formulation, processes, and method development activities. | 04/08/2021 |
| 9096 | Xilio Therapeutics Waltham, MA Associate Scientist, In Vivo Pharmacology MS in the field of immuno-oncology, or other related fields. Exp: 1-2+ years |
Individual will be responsible for conducting preclinical studies in animal tumor models (efficacy, PK/PD and MOA studies) to characterize immuno-oncology focused protein therapeutics. They will also perform downstream in vitro assays. | 04/08/2021 |
| 9097 | Ximedica Providence, RI Associate Mechanical Engineer BSME degree. Exp: 1+ year |
The Associate Mechanical Engineer with a minimum of 1+ year of experience product design and development. Any experience with complex, electro-mechanical products in the medical device arena is a plus. BSME degree is required. | 04/08/2021 |
| 9098 | Yokogawa Newnan, GA Application Engineer Bachelor’s degree in chemical engineering, electrical engineering or equivalent four-year engineering degree. Exp: 1-2 years |
As an application engineer your primary objective is to ensure the optimum ownership experience for Yokogawa customers by providing high-value technical support through clear, concise, and swift communication. | 04/08/2021 |
| 9099 | Zymo Research Irvine, CA Technical Manufacturing and QC Associate BS degree in Biochemistry, Microbiology, Genetics, Immunology, Virology, Molecular Biology or related field. Exp: 1-2 years |
Assist in the manufacturing of various chemicals, buffers, and other product-related components to ensure consistent product performance. Responsible for conducting quality control tests on various chemicals, buffers, and other product-related components. | 04/08/2021 |
| 9100 | Xyntek Newtown, PA Field Systems Engineer Bachelor’s degree in Electrical Engineering, Mechanical Engineering, Computer Engineering, or related fields. Exp: 0-1 year |
Engineering Technical Integration Services Team involved in deployment and commissioning of machine vision based automation equipment for packaging, sorting, shipping, etc.. within the logistics industry. and industrial systems control. | 04/08/2021 |
| 9101 | Zeteo Tech Sykesville, MD Chemist Bachelor's degree, chemistry preferred. Exp: 1 – 5 years |
Work in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your expertise to conduct chemical and physical laboratory tests to assist scientists in development of tools to detect and identify biological organisms and materials. | 04/08/2021 |
| 9102 | Zeteo Tech Sykesville, MD Microbiologist A degree in Microbiology, Biology, Biochemistry or another related science. Exp: 1-5 years |
Work in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your expertise to conduct biological laboratory tests to assist scientists in development of tools to detect and decontaminate biological organisms and materials. | 04/08/2021 |
| 9103 | Zeteo Tech Sykesville, MD Electrical Engineer Bachelors of Science Degree in Electrical Engineering, Computer Engineering, or other related technical field. Exp: 1+ years |
Seeking a skilled electrical or computer engineer with an interest in embedded systems. Developing game changing solutions to healthcare and national security challenges. You'll use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. | 04/08/2021 |
| 9104 | Accelerate Diagnostics Tucson, AZ Research Associate I, Quality Control Bachelor of Science degree in Microbiology, Biochemistry, Molecular Biology, Chemistry, or related life sciences. Exp: 1 year |
This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. | 04/09/2021 |
| 9105 | Accelerate Diagnostics Tucson, AZ Research Associate, Reagent Lab Bachelor’s degree in Chemistry, Molecular Biology, Microbiology, Biochemistry, or related field. Exp: Entry-Level |
Entry-level position in the Reagent Lab at Accelerate Diagnostics. Research Associates are responsible for conducting regular lab operations in the support of RUO, IUO, and IVD applications. A Research Associate in the Reagent Lab will contribute to planning and executing processes under GLP and cGMP guidelines (when applicable). | 04/09/2021 |
| 9106 | Accelerate Diagnostics Tucson, AZ Research Associate I (Second Shift) Bachelor's of Science in Microbiology or related field. Exp: 1 year |
The Research Associate is responsible for the day-to-day execution of experiments supporting assay development, technical operations, and core lab. This position can be in different teams including assay development, core lab and technical operations depending upon business needs. | 04/09/2021 |
| 9107 | Accurus Biosciences Richmond, CA Research Associate BS/MS in Biology. Exp: 0-3 years |
General molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. | 04/09/2021 |
| 9108 | Carmot Therapeutics Berkeley, CA Research Associate I/II , Biology BS/MS in cellular biology, biochemistry, molecular biology or related field. Exp: 1-4 years |
Identify new lead molecules by generating high-quality screening data using a variety of plate-based cellular and biochemical assays. Additionally, you will help develop new methods to interrogate compound mechanism of action, effect on cell signaling and physiology, and prioritize compounds for in vivo studies. | 04/09/2021 |
| 9109 | Comparative Biosciences Inc (Genesis Biotech) Sunnyvale, CA Histology Technician CBI BS degree in a scientific field; or diploma in Medical Technology or Histology certification by the ASCP or other professional organization preferred; Exp: 0-5 years’ |
The Histology Technician will possess the technical expertise to function effectively in a GLP toxicology and drug development environment. Skills in microtome sectioning (mandatory), embedding, staining and special staining. Provides support to other areas of CBI as qualified by training and/or experience. | 04/09/2021 |
| 9110 | Integrity Bio Thousand Oaks, CA Research Associate - Vaccine Stabilization Bachelor's degree in biochemistry, analytical chemistry, biological sciences, or related. Exp: 1-5 years |
Assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision. Handling and maintaining mammalian cell culture and perform biological activity assay by using aseptic technique. | 04/09/2021 |
| 9111 | Integrity Bio Thousand Oaks, CA Research Associate - Formulation Development Bachelor's degree in biochemistry, analytical chemistry, biological sciences, or related. Exp: 1-5 years |
Assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision. Set up and perform HPLC, as well as other assays, to characterize protein and peptide molecules. | 04/09/2021 |
| 9112 | Integrity Bio Camarillo, CA Manufacturing Associate BS in a Scientific discipline. Exp: 1 year |
Manufacturing Associate will be responsible for the manufacture of pre-clinical/clinical products Operates the production processes according to the determined daily production planning. Works according GMP regulations. | 04/09/2021 |
| 9113 | Lung Pacer Exton, PA Electrical Engineer MS in Engineering. Exp: 1+ years |
Support internal and/or external design activities to support development of new technologies and complete functional systems including manufacturing processes. - Prepare schematics, simulations, prototypes, PCB layouts, specifications, bills of materials, assembly drawings, and other documents as required to manufacture or support product. | 04/09/2021 |
| 9114 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1+ year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. | 04/09/2021 |
| 9115 | Spriaso Salt Lake City, UT Research Chemists Bachelor's degree in chemistry, chemical engineering, biochemistry, or other related degree concentration. Exp: 1+ year |
These positions entail doing product, process, and analytical functions in support of product and technology development under direction of product development and/or analytical leader. | 04/09/2021 |
| 9116 | Vaxess Technologies Cambridge, MA Research Associate, Immunology Master’s degree in one of the Life Sciences. Exp: 0-2+ years |
We are seeking a talented, collaborative, and highly motivated individual with expertise in immunology to join our core team of scientists and engineers. This is a unique opportunity to be part of an emerging startup bringing innovative technology to the global market. | 04/09/2021 |
| 9117 | AKESOgen Peach Tree Corners, GA Research Associate Bachelor’s degree in a clinical, health or life sciences field required. MS preferred. Exp: 1+ year |
This individual will perform extractions on a variety of sample types, genotyping on Affymetrix and/or Illumina platform equipment maintenance, solution and reagent preparation in addition to other tasks in laboratory. | 04/09/2021 |
| 9118 | Smith and Nephew Andover , MA Clinical Research Specialist Bachelors in a scientific or clinical/medical field required Exp: 0 - 2 years |
Experience in medical device industry, clinical study center setting or scientific/research field required. The Clinical Specialist I will support EU MDR related activities. This includes reviewing clinical evidence gaps, updating information on clinical gaps in the gap tracker. | 3/29/2021 |
| 9119 | Smiths Medical Minnesota, MN Design Assurance Engineer I University Degree (BA degree) required. 4-year engineering degree or similar. Exp: 0-3 years |
The Design Assurance Engineer I will be responsible for performing engineering work requiring full competency in all conventional aspects of engineering. | 3/29/2021 |
| 9120 | Solid Biosciences Cambridge, MA Associate Scientist, Molecular/Cell Biology BS/MS in Biology. Exp: 1 year |
Solid Biosciences is looking to hire an Associate Scientist to help our internal research efforts to advance our understanding of gene therapy. This is a hands-on lab position and will work directly with multiple project teams. | 3/29/2021 |
| 9121 | Sonoma Biotherapeutics San Francisco, CA Associate Scientist BS/MS with hands-on bench experience in Biological Sciences. Exp: 1-3 years |
Individual will assist in establishing the core’s capabilities to produce persistent and scalable human primary T cell processes, support research or translational programs and help with daily laboratory routines. | 3/29/2021 |
| 9122 | Sword Bio Chicago, IL Research Associate I BS or BA in biology, biochemistry or related field. Exp: 1-3 years |
Plan experiments with guidance from supervisor Perform complex and critical laboratory experiments (primarily ELISA) with accuracy and precision. | 03/31/2021 |
| 9123 | Synexus Rockville, MD Laboratory Associate Bachelor’s degree in Immunology, Biological Sciences, Biochemistry or an equivalent combination of education and experience. Exp: 1-3 years |
The Laboratory Associate collects blood samples from all subjects, processes samples to be shipped to outside laboratories and performs PBMC testing in the site laboratory. | 3/31/2021 |
| 9124 | Tenaya Therapeutics San Francisco, CA RA II Upstream PD (M.20) MS in a biological science or chemical engineering. Exp: 1-2 years |
Perform key production and characterization activities to support Upstream Process Development; routine productions; troubleshoot and optimize production unit operation and assays as needed. | 04/01/2021 |
| 9125 | Tenaya Therapeutics San Francisco, CA RA II, Upstream PD (M.17) M.S. with knowledge of general (bio) chemistry, cellular and molecular biology laboratory techniques. Exp: 1+ years |
Perform key production and characterization activities to support Upstream Process Development; routine productions; troubleshoot and optimize production unit operation and assays as needed. | 04/01/2021 |
| 9126 | Tenaya Therapeutics San Francisco, CA Research Associate I/ II - Biology/Gene Therapy BS/MS in Molecular Biology, Cell Biology, Biochemistry, or related discipline. Exp: 1+ years |
Execute a diverse range of cell-based and molecular assays to characterize lead gene therapy candidates. Functionally assess transduction and other gene therapy mechanisms in vitro and in vivo. | 04/01/2021 |
| 9127 | Tenaya Therapeutics San Francisco, CA Research Associate I / II, Gene Therapy BS/MS Exp: 1+ years |
Support the Gene Therapy team. Execute a diverse range of molecular biology, cell biology, and biochemistry assays to support the research of gene therapy targets. | 04/01/2021 |
| 9128 | Tenaya Therapeutics San Francisco, CA Research Associate I / II, QC Analyst BS/MS in Biology, Biochemistry, or related discipline. Exp: 0-2 years |
Support the Technical Operations Analytical Development/Quality Control Group. Perform key molecular biology and cell based assays to support Process Development and manufacturing activities; troubleshoot assays as needed. | 04/01/2021 |
| 9129 | Tenaya Therapeutics San Francisco, CA Research Associate I/II - Drug Discovery BS/MS in Biology, Biochemistry, or related discipline . Exp: 1+ years |
Execute a diverse range of cell-based and biochemical assays to characterize lead molecules and evaluate target function. Employ cutting edge molecular, cell, and biochemistry techniques to enhance drug discovery efforts. | 04/01/2021 |
| 9130 | Tenaya Therapeutics San Francisco, CA Research Associate I/II-Drug Discovery BS/MS in Biology, Biochemistry, or related discipline. Exp: 1+ years |
Execute a diverse range of cell-based and biochemical assays to characterize lead molecules and evaluate target function. Employ cutting edge molecular, cell, and biochemistry techniques to enhance drug discovery efforts. | 04/01/2021 |
| 9131 | Tenaya Therapeutics San Francisco, CA Research Associate, In Vivo Research BA/BS/MS in biology, physiology, pharmacology or related field. Exp: 1+ years |
Develop and validate pathophysiological heart disease models, including surgical or chemical induced and genetically modified models. Perform aseptic surgeries including preparation, surgical procedures, post and daily monitoring. | 04/01/2021 |
| 9132 | Tessera Therapeutics Cambridge, MA Research Associate, LNP Formulation BS/MS in Chemistry, Chemical Engineering, Bioengineering, Pharmaceutical Sciences or related discipline. Exp: 1-2 years |
Help support the lipid nanoparticle (LNP) formulation process and produce LNP-encapsulated RNAs and plasmids to support company’s in vitro and in vivo pre-clinical studies. | 04/02/2021 |
| 9133 | Tessera Therapeutics Cambridge, MA Research Associate, Analytical Development B.S. / M.S. or equivalent in a relevant discipline. (HPLC experience.) Exp: 1-2 years |
Join the analytical team to characterize synthetic oligonucleotides and mRNA with HPLC. Operate and maintain HPLC instruments. Perform assays and report results in appropriate format. | 04/02/2021 |
| 9134 | Teva Pharmaceuticals West Chester, PA Biological Researcher Masters in Biochemistry, Chemistry or related life sciences. Exp: 1+ years |
Exceptional opportunity for a Product Characterization Biological Researcher in the Analytical Sciences division. Understanding of protein molecule and some expertise with various analytical technologies. Experience on HPLC/UPLC based protein analytical methods in pharmaceutical and/or CRO industry. | 04/02/2021 |
| 9135 | Tolmar Ft Collins, CO Microbiologist I | 2nd Shift | Sunday - Wednesday BS Microbiology or closely related field. Exp: 1+ years |
Perform routine quality control/quality assurance product testing on pharmaceutical items under GMP and ISO conditions, mainly environmental monitoring, components and raw material testing. Record data accurately and consistently. | 04/02/2021 |
| 9136 | TriLink Biotechnologies San Diego, CA Research Associate BS in Molecular Biology, Biochemistry or Chemistry. Exp: 1-2 years |
Seeking a Research Associate. The dynamic Research will contribute to life science research at CDMO, specialized in mRNA and small molecule manufacturing. | 04/02/2021 |
| 9137 | TriLink Biotechnologies San Diego, CA Research Associate, Analytical Development BS in Chemistry, Biochemistry, Molecular Biology, Pharmaceutical, Life Science or equivalent. Exp: 0-2 years |
The entry-level Research Associate will be responsible for assisting with the development, optimization, and implementation of various analytical methodologies to support the analytical characterization of nucleic acids-based products manufactured at the company, such as nucleosides, nucleotides, oligonucleotides, DNA and RNA molecules. | 04/02/2021 |
| 9138 | Tri-Pac, Inc. South Bend, IN Associate Engineer BS in in engineering or life science. Exp: 0-2 years |
Support engineering activates like creating change control, executing validation documentation, writing deviations. Supporting in Writing Technical documents, Validation Summary Reports, and change control closeouts. | 04/02/2021 |
| 9139 | TSCAN Therapeutics Waltham, MA Research Associate (RA02-3) MS Exp: 1+ years |
Support our novel target identification and validation workflow in house, with focus on molecular cloning. The ideal candidate should have relevant experience in molecular biology, microbiology, high-throughput cloning, and enjoy fast-paced, collaborative and vibrant startup culture. | 04/02/2021 |
| 9140 | TSCAN Therapeutics Waltham, MA Research Associate/Senior Research Associate (RAO7-2) MS Exp: 1-3 years |
We are looking for an experienced researcher to join our team as Research Associate/Senior Research Associate, supporting the pre-clinical development of our lead programs. The ideal candidate should have relevant experience in primary T cell culture, immunoassays, flow cytometry, and molecular biology. | 04/02/2021 |
| 9141 | Twist Bioscience San Francisco, CA Research Associate, Process Development MS degree with industry experience in the following fields: Molecular Biology, Biochemistry, Genetics or a closely-related field. Exp: 1+ years |
Establish new processes at scale for DNA-based products in manufacturing. You will develop and support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput probe generation through robust experimental design. | 04/02/2021 |
| 9142 | Twist Bioscience San Francisco, CA Research Associate, Speciality Production B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
Support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. | 04/02/2021 |
| 9143 | Twist Bioscience San Francisco, CA Research Associate, Speciality Production B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
Support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. | 04/02/2021 |
| 9144 | Ultragenyx Pharmaceutical Cambridge, MA Temp Research Associate, Non-Clinical B.S. or equivalent degree in Biology, Molecular Biology, Biochemistry, Virology or related discipline. Exp: 1+ years |
Support the in vitro/in vivo Non-Clinical Team developing new AAV therapeutics for the treatment of rare diseases. | 04/02/2021 |
| 9145 | Frequency Therapeutics Lexington, MA Research Associate, Formulations MS in Chemical Engineering, Chemistry, Pharmaceutical Science, Physics, or Related Exp: 1+ Years |
The Research Associate, Formulations, is a laboratory-based position with tremendous learning potential in the area of drug formulation development. Reporting to the Associate Director, Process Development, and working in a cross-functional team environment, the successful candidate will take part in contributing to the development of the company’s PCA technology platform and executing the company’s small-molecule combination strategy. This position will be pivotal in the successful development of pharmaceutical products based on the company’s PCA platform. | 3/26/2021 |
| 9146 | Fresenius Kabi Grand Island, NY Associate Investigative Writer BS in Relevant Scientific Discipline Exp: 1-2 Years |
Works with Supervision and Investigative Writers to efficiently and thoroughly investigate deviations and customer complaints, determination of root cause, and initiation of corrective/preventative actions designed to adequately address and correct the quality related deficiencies identified during the investigation process. Responsible to recommend proactive corrections, corrective actions and preventative actions based on noted trends to minimize the potential for repeat incidents that may lead to, or result in, the issuance of product discards, field actions, or recalls. The position requires working with moderate supervision to manage assigned investigations from initiation to completion. | 3/26/2021 |
| 9147 | Fresenius Kabi Melrose Park, IL Aseptic Process Mentor BS in Microbiology or Life Sciences Exp: 1-3 Years |
Responsibilities: Monitors aseptic core to ensure continual compliance with GMP's and provides mentoring on aseptic technique with operators. Reports metrics to site management on a regular basis. Monitors Filling Operators by completing daily visual audits of Aseptic Behavior inside the core during fills and lyophilizer loading. Partners with Production/Quality/Training Leadership to make recommendations for enhancements to aseptic process. | 3/26/2021 |
| 9148 | Fresenius Kabi Grand Island, NY QC Tech II Micro BS in Relevant Scientific Discipline Exp: 0+ Years |
This individual holding the position of QC Technician II shall be responsible for performing routine testing of in-process and finished product samples, raw material, stability, and utilities. They shall be responsible for monitoring the environmental conditions in the laboratory and in manufacturing areas. They shall support validation projects. This position must be available to work overtime as assigned. | 3/26/2021 |
| 9149 | Fresenius Kabi Melrose Park, IL Scientist MS in Chemistry or Related Exp: 0-3 Years |
Fresenius Kabi currently haa an opportunity for a Scientist, who will conduct all aspects of Analytical Development including method development, experimentation, and record keeping, including developing and implementing methods that meet project needs. | 3/26/2021 |
| 9150 | Fresenius Kabi Grand Island, NY Associate Scientist BS in Chemistry, Biology, or Related Exp: 1-3 Years |
The incumbent is responsible for routine calibration and preventative maintenance in the Quality Control laboratories. Reports to QA Metrology Manager. Duties are of routine nature and are followed according to established standard operating procedures. Problem recognition ability is needed. Non-critical functions utilize independent action and decision making with follow-up reporting to supervision. Supervisor directly responsible for training, assignment of duties and review/approval of work. Direction, training and some day-to-day supervision may also come from a Scientist or Lead Scientist. Effectively communicates work and results both orally and in writing. | 3/26/2021 |
| 9151 | Fresenius Kabi Melrose Park, IL Aseptic Filling Operator III BS in Engineering or Sciences Exp: 0+ Years |
Technician will be responsible for assembling, operating and monitoring a state of the art, aseptic filling machine in accordance with applicable Standard Operating Procedures and current Good Manufacturing Practices. Must be knowledgeable of and practice good aseptic technique to minimize potential for product contamination as well as understand advanced computerized systems through HMI. | 3/26/2021 |
| 9152 | Fresenius Kabi Grand Island, NY QC Technician BS in Relevant Scientific Discipline Exp: 0+ Years |
This position serves in the capacity of performing general laboratory tasks of testing finished products, stability, raw material, utilities, and monitoring for environmental control, as well as supporting validations of rooms, equipment and materials. This position reports to the supervisor for the functional area to which they are assigned and has no direct reports. The QC Technician II position works closely with other departments, such as validations, chemistry, Operations, Product Development, Quality Systems and Product Release to assure the support of the Microbiology department on various projects, studies and routine tasks. | 3/26/2021 |
| 9153 | Frontage Eagleview, PA Associate Scientist/Scientist BS/MS in Relevant Scientific Discipline Exp: 1-5 Years |
This is a technical scientific position within the Study Bioanalysis Team. The Study Bioanalysis Team is responsible for conducting bioanalytical methods related to large molecule biotherapeutic drug development across all therapeutic areas, spanning nonclinical studies to post-market clinical development. Responsibilities: Performs job duties with some supervision, with majority of interaction with direct supervisor and project team members. Collaborates effectively with fellow project members following priorities, checkpoints and timelines in support of objectives set by direct supervisor. Explains work with independent analysis and conclusions related to assigned tasks through written and oral communication | 3/26/2021 |
| 9154 | Frontage Exton/Remote, PA Proposal Analyst - Central Laboratory Services BS in Relevant Scientific Discipline Exp: 1-2 Years |
Responsibilities: Perform clinical trial study protocol analysis, generate quote, prepare and review proposals/contracts, and keep track of the status of potential incoming projects. Working closely with the clinical operation team and develop the Cost Per Test Table. Participate and communicate effectively in the client and internal meetings. Generation of clinical trial related documentation as needed and per client request. Support Management and BD team for new business opportunities and assist with all functions of Clinical Trials Proposal and Budget generation, providing support for all Clinical Trials Business Development staff. Assist to ensure all areas of proposal and budget development, including development and maintenance of Standard Operating Procedures. Maintain a general working knowledge of phase I-IV clinical trials and basic laboratory terminology. | 3/26/2021 |
| 9155 | Frontage Eagleview, PA Scientist 008 MS in Bioengineering, Biotechnology, or Related Exp: 1+ Years |
Responsibilities: Provide high-quality analytical testing of finished products, raw materials, Active Pharmaceutical Ingredient (API), in-process products and stability samples; provide analytical method development, validation and verifications in Good Manufacturing Practice (GMP) environment; perform analysis of innovator samples and R&D formulations; compile and interpret analytical and statistical data; review and approve protocols, laboratory notebooks, reports, deviations, Out of Specification (OOS) and Out of Tolerance (OOT) investigations, specifications, and analytical documents for method validation and ANDA submissions. | 3/26/2021 |
| 9156 | Frontage Concord, OH Quality Control Technician BS in Relevant Scientific Discipline Exp: 1+ Years |
Responsibilities: Provide support to Study Directors and Program Managers for the purpose of facilitating study operations, report production and program oversight. Address problems, conflicts, or difficulties that pertain to assigned studies and negotiate and/or implement solutions. Detail oriented delegated duties. Data entry of pertinent quality control and data set information. Review and organize research data sets for the purpose of Quality Control. Create control documents, test procedures, SOPs, etc. as needed. Draft study documents including forms, protocols, amendments, reports, etc. Edit, compile, and/or format documents. Assist with report finalization by collecting signatures, document management, CD/flash drive preparation, and archiving. | 3/26/2021 |
| 9157 | Frontage Concord, OH Lab Technician BS in Microbiology or Related Exp: 0+ Years |
This position will provide technical support for performing standard in vitro assays to include, but not limited to cell-based assays, bacterial production and characterization, microscopy, PCR, as well as other in vitro-related activities. | 3/26/2021 |
| 9158 | Frontage Exton, PA Medical Technologist BS in Medical Technology or Clinical Laboratory Science Exp: 0-2+ Years |
Responsibilities: Validation and verification studies of new instrumentation and methods. Establish and maintain standard operating procedures for designated methods. Perform maintenance and quality control for all instrumentation and methods. Troubleshoot and repair instrumentation, liaise with service engineers and instrument vendors. Adhere to safety and quality procedures, participate in Proficiency Testing, maintain competency on all instrumentation (six month and annual). Sample analysis including Chemistry, Hematology, Urinalysis, Coagulation, Molecular, and COVID-19 testing. | 3/26/2021 |
| 9159 | Frontage Exton, PA Associate Scientist - Product Development - CMC MS in Pharma, Microbiology, Chemical Engineering, or Related Exp: 0-4 Years |
Responsibilities: Perform assigned tasks per procedures compliant with cGMPs and participate in the clinical manufacturing of parenteral, ophthalmic, and other sterile dosage forms. Participate in media fills for aseptic fill projects. Assist in the equipment set up, operation, maintenance, cleaning as required for the project. Perform Environmental Monitoring (EM) of manufacturing areas per applicable SOPs and maintain records. Assist with manufacturing area maintenance such as area monitoring and qualification, purchase of gowning supplies, purchase of equipment and room cleaning supplies, microbiological monitoring supplies. Maintain records for personnel gowning qualification. Execute product development studies under the guidance of supervisor or lead project scientist to support formulation development (R&D), and clinical drug product manufacturing. | 3/26/2021 |
| 9160 | Fulcrum Genomics Phoenix, AZ Computational Biologist/Bioinformatics Scientist BS in Biology, Computer Science, or Related Exp: 0+ Years |
The Bioinformatics Scientist will provide data analysis and expert advice regarding genomics and biology. This position will work directly with the Fulcrum Genomics team, including the Founding Partners, and its clients to define and execute on client-based bioinformatics data analysis projects and tasks. | 3/26/2021 |
| 9161 | GBT San Francisco, CA Research Associate, Pharmacology BS in Pharmacology, Hematology, or Related Exp: 0-2 Years |
Responsibilities: Perform in vivo pharmacology studies with hematological disease models and conduct in vivo drug efficacy studies to support early drug discovery projects. Develop and troubleshoot novel in vivo disease models for mechanism of action studies. Plan, execute, analyze, and document experiments. Work in a team environment. | 3/26/2021 |
| 9162 | GBT San Francisco, CA Development Risk Manager BS in Life Sciences or Related Exp: 0+ Years |
This Program Manager will be accountable for proactively identifying and assessing compliance risks. They will create a portfolio of projects and work closely with the Director of Clinical Operations Excellence to manage through to completion. They will also proactively monitor emerging regulations and policies and ensure GBT proactively monitors and mitigates risks. | 3/26/2021 |
| 9163 | GDIT Fort Sam Houston, TX Research Technician II BS/MS in Relevant Scientific Discipline Exp: 0-1 Years |
GDIT is seeking a Research Technician II or III level in support of the Naval Medical Research Unit, San Antonio Texas (NAMRU-SA) to support the conduct of the following research areas: expeditionary and trauma medicine, cellular and immune based adjuncts for casualty care, directed energy and bioeffects, systems engineering and evaluation, epidemiology and biostatistics, environmental surveillance and biomaterials, and maxillofacial injury and disease | 3/26/2021 |
| 9164 | GDIT Washington, D. Research Analyst Associate BA/BS in Social Sciences Exp: 1-2 Years |
This position will support the Association of American Medical Colleges’ MCAT program full time. The Medical College Admission Test® (MCAT®) is a standardized, multiple-choice, computer-based test that has been a part of the medical school admissions process for more than 90 years. Each year, more than 85,000 students sit for the exam. The MCAT exam tests examinees on the skills and knowledge that medical educators, physicians, medical students, and residents have identified as key prerequisites for success in medical school and practicing medicine. | 3/26/2021 |
| 9165 | Seres Therapeutics Cambridge, MA Associate II, Bioprocessing MS in Microbiology, Molecular Biology, Chemical Engineering, Biotechnology or a related field. Exp: 0-2 years |
Person will be involved in development of different processes for cell banking and fermentation, as well as novel assays to track upstream and downstream process development. This individual will also collaborate with Manufacturing Sciences to support the transfer of processes to manufacturing operations. | 3/23/2021 |
| 9166 | Seres Therapeutics Cambridge, MA Associate II, Manufacturing BS in Life Sciences or Biotechnology Certificate with 0-1 years' experience in Biotech manufacturing. Exp: 0-1 years |
Person will be responsible for supporting manufacturing operations and clinical supplies across several phases of clinical trials. This individual will be involved in the execution and documentation of cGMP manufacturing processes, and operations pertaining to drug substance and drug product manufacturing. | 3/23/2021 |
| 9167 | Seres Therapeutics Cambridge, MA Associate, Donor Analytical Sciences BS Life Sciences, Biotechnology or a related field. Exp: 1-2 years |
Person will responsible for laboratory assays to examine and characterize donor microbiomes. This position also oversees activities related to biological sample analysis, inventory, and management. | 3/23/2021 |
| 9168 | Seres Therapeutics Cambridge, MA Associate, Quality Control BS in microbiology, molecular biology, biochemistry or a related discipline. Exp: 1-2 years |
Seeking proactive team player and rapid learner with strong positive attitude who is excited about learning and applying new skills while also potentially making a difference in people’s lives, this may be the role for you. | 3/23/2021 |
| 9169 | Seres Therapeutics Cambridge, MA Research Associate, Immunology BS/MS in Biology (or equivalent). Exp: 1- 3 years |
Candidate will have lab research experience in immunology, immuno-oncology or related fields within academic or industry settings. This person will be responsible for a wide range of experiments with a primary focus in the immuno-oncology and inflammatory disease areas. | 3/23/2021 |
| 9170 | Seres Therapeutics Cambridge, MA Research Associate, Microbiology & Functional Screening BS or Masters in immunology, cancer and cell biology or related scientific field. Exp: 1+ years |
Relevant work experience required. Join our Microbiology and Functional Screening team to develop and implement high throughput functional screens that advance the company’s Ecobiotic® therapeutics discovery programs in oncology, infectious and inflammatory diseases. | 3/23/2021 |
| 9171 | Siegfried Pennsville, NJ QC Chemist I (In Process) BS in Chemistry or related science. Exp: 0-5 years |
The Incumbent has knowledge and experience applying basic scientific principles and routinely performs analysis in the following functional areas (HPLC, GC, and Wet Chemistry). The incumbent is able to troubleshoot and participate in investigations. | 3/24/2021 |
| 9172 | SRI Biosciences Menlo Park, CA Bioscience Research Associate I BS degree in Biological Sciences or equivalent scientific discipline. Exp: 0-2 years |
Assist in advancing candidate therapeutics, vaccines, and prophylactics through preclinical development. Provide technical support for genetic toxicology and molecular biology studies. | 3/25/2021 |
| 9173 | Stemexpress East Norriton, PA Clinical Laboratory Scientist (PA) BS degree in Medical Technology or Biological Sciences from an accredited college or university. Exp: 0-3 years |
Laboratory activities include pooling plasma/buffy coats; processing; identifying; sorting; and tracking various specimens in adherence to all applicable regulatory requirements. | 3/25/2021 |
| 9174 | T2 Biosystems Lexington, MA Research Associate - Microbiology B.S. in Microbiology or Molecular Biology Exp: 0-1 year |
Responsible for providing general expertise in the areas of microbiology and bacterial physiology. | 3/25/2021 |
| 9175 | Tenaya Therapeutics San Francisco, CA RA I/II, QC Analyst BS/MS in Biology, Biochemistry, or related discipline. Exp: 0-2 years |
Perform key molecular biology and cell based assays to support Process Development and manufacturing activities; troubleshoot assays as needed. | 3/25/2021 |
| 9176 | Therapeutics Inc. San Diego, CA Clinical Data Associate BS degree or equivalent. Scientific background. Exp: 0-2 years |
Provide support to the Data Management (DM)department. This will include administrative tasks, data entry of clinical trial data into study databases, participation in database validation. | 3/25/2021 |
| 9177 | Tri-Pac, Inc. South Bend, IN Associate E ngineer BS Degree in Engineering or Life science. Exp: 0-2 years |
Support engineering activates like creating change control, executing validation documentation, writing deviations. Supporting in Writing Technical documents, Validation Summary Reports, and change control closeouts. | 3/26/2021 |
| 9178 | Twist Bioscience San Francisco, CA Research Associate B.Sc. in Chemistry, Analytical Chemistry, Molecular Biology Exp: 0-2 years |
Develop analytical methods for QC of incoming reagents for DNA synthesis. Collecting, organizing and presenting data to senior managers with the goal of improving DNA synthesis quality. | 3/26/2021 |
| 9179 | Twist Bioscience San Francisco, CA Research Associate, Cell Biology B.S./ MS degree in cell biology, immunology, protein biochemistry, biological chemistry, or related discipline. Exp: 0-2 years |
Work within a team responsible for antibody discovery utilizing a number of in vitro display technologies, e.g. phage display, ribosome display, and yeast display. | 3/26/2021 |
| 9180 | Vedere Bio Cambridge, MA Research Associate Master’s degree in Biological or related fields with a 0+ year industrial experience. Exp: 0+ years |
Work with the Research Team to support our viral vector production processes and run assays in support of the portfolio of AAV-based programs at Vedere Bio. | 3/26/2021 |
| 9181 | Vedere Bio II, Inc. Cambridge, MA Research Associate, Research and Process Analytics Bachelor’s degree in Biological or related fields. Exp: 0+ years |
Join the Analytical Development group and support routine analytical testing of research and process development samples. Highly cross functional role involves running a panel of assays on a weekly basis. | 3/26/2021 |
| 9182 | Biotechne Minneapolis, MN Quality Assurance Specialist MS in Relevant Scientific Discipline Exp: 0-2 Years |
The Quality Assurance Specialist provides training and quality-related guidance to Bio-Techne’s staff through extensive understanding of compliance standards and governing bodies. This position will lead quality assurance best practices and work with department leaders to implement improvements. Prior quality assurance experience within a similar industry, as well as strong attention to detail are key attributes to being successful in this role. | 3/19/2021 |
| 9183 | Biotechne Devens, MA Manufacturing Technician BS in Relevant Scientific Discipline Exp: 0+ Years |
The Manufacturing Technician is responsible for operating manufacturing equipment and complete all documentation according to cGMP/ISO standards. Provide written documentation of required data throughout the manufacturing operations in accordance to established SOPs, Work Instructions and cGMPs/ISO standards. Provide hands on assistance as needed on equipment lines and manual pack lines. | 3/19/2021 |
| 9184 | Biotechne Minneapolis, MN Senior Research Associate, QC Immunoassays MS in Biology, Chemistry, Biochemistry, or Related Exp: 0-2 Years |
The responsibilities of this position are to perform ELISA assays to check for quality performance of product, maintain accurate documentation of results, and maintain assay databases. This position will perform quality control testing of Quantikine ELISAs, Luminex assays, IVD kits, and related product lines. Formulate solutions for production and raw material testing as needed. Perform raw material qualification testing as needed. Calculate data and compile results efficiently. Troubleshoot assay problems and collaborate with others. Assist in transfer of new products from Development. Perform general lab duties as needed. Within this job function, the Senior Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company.The responsibilities of this position are to perform ELISA assays to check for quality performance of product, maintain accurate documentation of results, and maintain assay databases. This position will perform quality control testing of Quantikine ELISAs, Luminex assays, IVD kits, and related product lines. Formulate solutions for production and raw material testing as needed. Perform raw material qualification testing as needed. Calculate data and compile results efficiently. Troubleshoot assay problems and collaborate with others. Assist in transfer of new products from Development. Perform general lab duties as needed. Within this job function, the Senior Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. | 3/19/2021 |
| 9185 | Biotechne Minneapolis, MN Technical Services Associate BS in Biological Sciences, Biochemistry, or Equivalent Exp: 0-2 Years |
The responsibilities of this position (Technical Service Associate – TSA) are to respond to incoming technical inquiries providing first tier technical and sales assistance on all Bio-Techne brands. Complete all customer requests including e-mail responses and simple quotes. Maintain technical resources. Back up Customer Care and Sales departments. Continue training to stay up to date on technical information for old and new products. Perform additional duties as assigned. | 3/19/2021 |
| 9186 | Biotechne Minneapolis, MN Research Associate, Antibody Purification BS in Biotechnology or Relevant Discipline Exp: 0-2 Years |
This position is responsible for purifying polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, other products used by pharma and IVD customers. Purifies polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. This person will be expected to either work a Sunday to Thursday or Tuesday to Saturday shift. | 3/19/2021 |
| 9187 | Biotechne Minneapolis, MN Advanced Research Associate MS in Biology or Related Exp: 1-2 Years |
This position is the point of contact for coordinating sample testing with internal and external service providers. They would assist in evaluating testing requirements based on customer needs as well as assisting in internal testing and evaluation of data. | 3/19/2021 |
| 9188 | Biotechne Minneapolis, MN Reseach Associate BS in Relevant Scientific Discipline Exp: 0-3 Years |
A Research Associate is responsible for development of cell culture protocols for new recombinant protein products. This includes screening clones and testing growth conditions in bioreactors and other culture formats, in small to medium scale. It may also include cooperation with the molecular biology group in creation of new clones and clone libraries, creation and characterization of new cell lines, and screening studies in search for novel protein product targets. | 3/19/2021 |
| 9189 | Expansion Therapeutics Jupiter, FL Research Associate BS in Relevant Scientific Discipline Exp: 1+ Years |
The candidate will perform non-routine and semi-complex research in the laboratory as a Research Associate, applying relavant knowledge and techniques to support the Scientific staff. | 3/19/2021 |
| 9190 | Exscientia Miami, FL AI Research Engineer MS in AI, Machine Learning, Mathematics, Physics, or Related Exp: 0+ Years |
In this role, you will be using your scientific expertise to directly contribute to Exscientia's mission: making better drugs, faster - by further improving the predictive and generative modeling capabilities of their AI technology platform. They are applying state-of-the-art AI methods to address a diverse range of important problems in drug discovery and are constantly innovating if required tools are not sufficient or do not exist. Their ambition is to draw knowledge and inspiration from additional scientific disciplines such as mathematics, physics or computer science. | 3/19/2021 |
| 9191 | Fitzpatrick Rochester, NY Application Engineer BS in Mechanical or Chemical Engineering Exp: 0-2 Years |
The Application Engineer provides technical support related to the sale of the company’s engineered products based on the industrial process and application details. The Application Engineer will become a process and application expert where Pulsafeeder equipment is used and identify potential growth opportunities. This individual will respond to technical inquiries from customers, both domestically and internationally, company sales reps, and distributors, in a timely manner, and assist in the order attainment process. The Application Engineer will manage sales inquiries through preliminary engineering, costing, pricing, quoting, and follow up to key proposals. This position is also responsible for assisting Order Entry personnel in problem resolution; review of drawing submittals, and in solving technical issues. Key business measures such as quotation and order activity of assigned rep and distributor offices will be monitored with appropriate follow up, assistance, and guidance to assist in obtaining orders. The Application Engineer will work with Sales and the Senior Leadership Team to help to create and track large opportunities in the sales funnel and will participate on forecast calls to share feedback and opportunities for growth. | 3/19/2021 |
| 9192 | Fitzpatrick Denver, CO Manufacturing Engineer 1 MS in Mechanical Engineering, Industrial Engineering, or Related Exp: 0+ Years |
As a Manufacturing Engineer I, you will help direct, coordinate and actively participate in creating a sustainable culture of continuous improvement with a focus on the manufacturing process. Creating cell layouts and optimizing operational KPIs will be a core focus on your daily activities. Key responsibilities include the identification of waste within Fitzpatricks current state and developing a repeatable, reliable and efficient solution targeted at eliminating the waste. The Manufacturing Engineer I will prioritize and deploy engineering techniques and Lean solutions across the factory to meet key Safety, Quality, Delivery, and Cost targets. This role comes with the autonomy to problem solve, the support of leadership to drive implementation, and the capital backing to create world class manufacturing techniques and processes. | 3/19/2021 |
| 9193 | Fitzpatrick Waterloo, On Trade Compliance Specialist BS in Relevant Scientific Discipline Exp: 1-3 Years |
The ideal candidate shows good judgement and instinct in decision making with a drive for continual improvement of business operations and trade compliance awareness. This is an exciting position that will be leading global strategy, development and implementation of process improvements, and ongoing Group and Business Unit compliance program efforts supporting Fitzpatrick's rapidly growing and evolving businesses. | 3/19/2021 |
| 9194 | Fitzpatrick Wooster, OH Electrical Project Engineer BS in Electrical Engineering or Engineering Technology Exp: 0+ Years |
Responsible for design, integration, and project management of custom engineered systems for remote controlled monitors (water cannons) for the industrial (petrochemical) market. Duties include but are not limited to, control panel design, develop PLC programs for site specific requirements and integration, on site start-up, and customer training and after sales technical support. | 3/19/2021 |
| 9195 | Fitzpatrick Ocala, FL Web-App Architect/Engineering BS/MS in Computer Science, Engineering or Equivalent Exp: 0+ Years |
The purpose of the Web-App Architect/Engineer role is to design and deliver a high-quality, secure, and tightly integrated user experience as part of a high-performance solutions development team. The primary responsibilities will be to create a globally deployable user experience within IDEX Fire & Safety’s Captium data platform. To succeed in this role, you will have a passion for scalable, Agile software development, foster a culture of collaboration and innovation, and deploy highly reliable and intuitive data solutions that create value for our customers. | 3/19/2021 |
| 9196 | Fitzpatrick Westwood , MA Applications Engineer BS in Chemical Engineering, Bioengineering, Biochemistry, or Related Exp: 1-3 Years |
This is a full-time position in which you will be working in the Microfluidics Applications Laboratory. In this role, you will utilize various models of Microfluidics processing equipment to process customer samples of dispersion or emulsion materials within a variety of industries such as pharmaceutical, biotech, chemical, nutraceutical, and cosmetics. You will also test mechanical components using standardized testing procedures. Additional responsibilities include interacting with Sales, Marketing, Customer Service, and providing assistance to the Engineering and Operations Departments through research and analysis of test data. | 3/19/2021 |
| 9197 | Forge Biologics Grove City, OH Technician, Research Manufacturing BS in Biological Sciences or Engineering Exp: 0+ Years |
This position reports to the Manager of Research Manufacturing and is responsible for the production of recombinant adeno-associated virus (rAAV) vectors via maintenance of mammalian and insect cell lines, transfection, infection, and downstream purification of rAAV by chromatography and ultracentrifugation. You will utilize shake flasks and bioreactors for scale up experiments. You will also be directly involved in scalable downstream purification technologies for rAAV using FPLC systems, tangential flow filtration, and centrifugation. Work activities will also include compiling experimental data and contributing to protocols and study reports with supervision. It is expected that you will work as a member of the production team while accomplishing the timely completion of assignments and reporting of unexpected technical issues. | 3/19/2021 |
| 9198 | Forma Therapeutics Watertown, MA Research Associate, Translational Science BS/MS in Biology or Related Exp: 0+ Years |
Responsibilities: Develop, optimize and perform assays using molecular biology procedures and technologies including qPCR, quantitative western blots, ELISA. In vitro culture of cancer cell lines and primary cells as well as DNA/RNA isolation from blood/tissue is required. Assist in the management of preclinical and clinical samples internally and with third party providers. Generate and analyze experimental data and present to key stakeholders. | 3/19/2021 |
| 9199 | Freenome San Francisco, CA Clinical Laboratory Assistant, Analytical Laboratory BS in Biological Science or Related Exp: 0+ Years |
Freenome’s Clinical Laboratory Assistant will support the company’s Pre-Analytical Laboratory with the receiving, accessioning, plasma sample processing, and storage. Providing quality samples to process downstream for quality analysis and results is important to their mission. | 3/19/2021 |
| 9200 | Freenome San Francisco, CA Clinical Laboratory Associate BS in Biological Science or Related Exp: 0+ Years |
Freenome’s Clinical Laboratory Associate will support the company’s Pre-Analytical Laboratory with the receiving, accessioning, plasma sample processing, and storage. Important to our mission is providing quality samples to process downstream for quality analysis and results. | 3/19/2021 |
| 9201 | Freenome San Francisco, CA Clinical Laboratory Scientist BS in Biomedical Laboratory Science, Clinical Science Exp: 1+ Years |
As a Clinical Laboratory Scientist you will join a highly collaborative team and make an immediate impact on early cancer detection. You will support Freenome’s mission by performing high complexity laboratory testing (Next Generation Sequencing) on study specimens, performing quality control and quality assurance procedures, and comply with all applicable local, state and federal laboratory requirements. The work requires keeping meticulous and organized records, excellent attention to detail, the ability to prioritize and be flexible with multiple tasks and schedules. | 3/19/2021 |
| 9202 | Encodia San Diego, CA Research Associate (Assays) MS in Molecular Biology, Biochemistry, or Related Exp: 0-2 Years |
Encodia is seeking to recruit a Research Associate with a background in molecular biology, biochemistry and assay development. The successful candidate will be responsible for performing experiments to optimize protein- and DNA-based assays. An individual, who is highly motivated, detailed-oriented and willing to work in a fast paced environment, is encouraged to apply. | 3/12/2021 |
| 9203 | Encodia San Diego, CA Research Associate - Protein Purification MS in Molecular Biology, Biochemistry, or Related Exp: 0-2 Years |
The successful candidate will support Encodias large scale protein and protein bioconjugate production efforts, as well as other developmental areas. Additionally, the successful candidate will be working with a cross functional team to support core needs of various departments within the company. | 3/12/2021 |
| 9204 | Encodia San Diego, CA Research Associate - Chemistry Department MS in Biotechnology or Pharmaceutical Related Discipline Exp: 0+ Years |
Encodia is seeking to recruit a Research Associate to join their highly-innovative Chemistry team. The successful candidate will have a diverse range of organic chemistry experience applied in a high-throughput discovery environment. The ideal candidate will have a strong foundational knowledge in the fundamentals of organic chemistry and chemical biology, and be highly motivated to apply these tools to innovating Next-Gen tools in proteomics. | 3/12/2021 |
| 9205 | Encodia San Diego, CA Research Associate (Protein Engineering) BS in Molecular Biology, Biochemistry, or Related Exp: 0-2 Years |
Encodia is seeking a highly motivated Research Associate with 0 - 2 years of dedicated bench-work experience with Protein Engineering or related areas. The successful candidate will possess a BS degree in Molecular Biology, Biochemistry or a related field and possess excellent laboratory skills in protein engineering or assay development. Responsibilities: Constructing high diversity DNA libraries and performing directed evolution experiments. Running high-throughput molecular assays. Preparing NGS samples and analyzing sequencing data. Performing independent data analysis and communicating results. | 3/12/2021 |
| 9206 | Endo International Horsham, PA Manufacturing Associate II, Downstream Processing BS in Relevant Discipline Exp: 1-3 Years |
The Manufacturing Associate II, Downstream Processing works in a hands-on capacity in the cGMP purification and production support areas to manufacture collagenase clostridium histolyticum bulk drug substance (CCH BDS). This role authors and revises manufacturing & process documentation and is responsible for supporting necessary purification and production-related activities, including validation and development work as needed. | 3/12/2021 |
| 9207 | Endo International Horsham, PA Manufacturing Associate II, Upstream Processing BS in Relevant Discipline Exp: 1-3 Years |
The Manufacturing Associate II, Upstream Processing works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture collagenase clostridium histolyticum bulk drug substance (CCH BDS). This role authors and revises manufacturing and process equipment documentation and is responsible for supporting necessary fermentation and production activities, including validation and development work as needed. | 3/12/2021 |
| 9208 | Endo International Horsham, PA QC Analyst I - Microbiology BS in Biological Science or Related Exp: 0-3 Years |
The QC Analyst I – Microbiology will perform microbiological testing, release of in-process, intermediates and finished products, and testing for validation purposes. This role completes appropriate documentation to support testing procedures including data capture forms, equipment logbooks, and inventory forms. Additionally, this role is responsible for assisting with the writing of standard operating procedures (SOPs) and revision of existing documentation. | 3/12/2021 |
| 9209 | Endo International Horsham, PA QC Analyst II - Chemistry MS in Biological Science or Related Exp: 1-3 Years |
The QC Analyst II - Chemistry will provide bioanalytical expertise for the Quality Control (QC) department. Key areas of focus are development and implementation of the quality aspects of late stage or marketed product strategy. This role is involved with performing and assisting with OOS investigation and resolution. Additionally, the Analyst II will have responsibility for coordinating the bioanalytical technology transfer from outside departments and to outside contractors. | 3/12/2021 |
| 9210 | Endo International Horsham, PA Quality Specialist MS in Scientific or Engineering Discipline Exp: 1+ Years |
The Quality Specialist assists with internal and external quality operations and systems, such as facility/equipment, utilities, materials, production, laboratory, packaging/labeling, and general compliance as applicable, and helps assure compliance with current domestic and international GMPs and regulatory agencies. The Quality Specialist may monitor, track and trend Non-Conformances, CAPA and other quality systems, assesses the risk level associated with Non-Conformances and escalate the issue to management. This role is responsible for initiating self-audit checks and evaluation of CAPA effectiveness checks. Additionally, the Quality Specialist is responsible for preparing materials for inspection readiness and management review. | 3/12/2021 |
| 9211 | Endpoint Wakefield, MA Quality Engineer BS/MS in Scientific Discipline Exp: 0+ Years |
The Quality Engineer, reporting to the Director, Quality Management, is a driver of exceptional product quality, reliability, and security through directly influencing Product Development, Operations, and IT builds. This individual actively participates in risk management, design controls, design for quality, design for maintainability, design for supportability, and product validation. They ensure upper management is apprised on the performance of the quality management system and any need for improvements. The quality engineer also promotes awareness of regulatory and customer requirements throughout the organization and leads focused quality projects, as required, to resolve problems or make improvements to specific processes. | 3/12/2021 |
| 9212 | Endpoint San Francisco, CA Data Specialist BS in Relevant Discipline Exp: 1-2 Years |
The Data Specialist will support all aspects of Data Management at endpoint, including data changes, verification, data transfers, and data integrations with supporting documentation. The person in this role will work independently with minimal guidance from the Senior or Lead Data Specialist. The role requires interaction with internal study teams and occasionally with external end users and sponsors. | 3/12/2021 |
| 9213 | Entrada Therapeutics Boston, MA Research Associate I, Neuromuscular and Cardiac Biology BS/MS in Cell Biology, Molecular Biology, or Related Exp: 0+ Years |
In this position, you will be part of a cross-functional team exploring new therapeutic programs for neuromuscular and cardiovascular disease areas. You will play a critical role in the development and execution of molecular and cellular biology experiments which are critical to the success of Entrada's drug discovery programs. You will utilize cell-based disease models, and techniques such as PCR, Western blot, cell and tissue culture, and immunostaining (IHC, IF). | 3/12/2021 |
| 9214 | Entrada Therapeutics Boston, MA Analytical Research Associate I/II BS/MS in Biochemistry, Bioscience, Biotechnology, or Related Exp: 1+ Years |
Under the supervision of the Senior Level Scientist, you will work very closely with CMC process development, analytical method development, formulation development, and discovery to perform analytical testing to facilitate the process development, formulation, DS release and stability program. You will perform HPLC/UPLC, CE based assays for the determination of purity, charge isoforms, and impurities for the process intermediates, drug substance, and drug product. You will also be involved in cross functional team meetings, be given the opportunity to present your work to key stakeholders, and broaden your analytical skills and instrumentation knowledge. | 3/12/2021 |
| 9215 | Entrada Therapeutics Boston, MA Research Associate II/Senior Research Associate, Discovery Chemistry BS/MS in Organic Chemistry, Analytical Chemistry, or Related Exp: 0+ Years |
In this role you will be responsible for designing and executing the synthesis and purification of peptides and oligonucleotide development candidates. You will also integrate and execute analytical characterizations of peptide and oligonucleotide libraries using liquid chromatography techniques and LC-MS. Along with these responsibilities, you’ll also be responsible for maintaining good written records of laboratory procedures, data analysis, and generate high-quality study reports, performing routine instrument maintenance and buffer preparations. You should be excited to interpret and present your research findings at scientific meetings. | 3/12/2021 |
| 9216 | Envisagenics New York, NY Bioinformatics Analyst MS in Bioinformatics or Related Exp: 0+ Years |
The candidate will be responsible for building pipelines and creating tools to manage large volumes of sequencing data and will assist with generating and assessing meta-data to support internal R&D efforts. The ideal candidate will have experience with analysis of large datasets, knowledge of tools and biological databases, SQL knowledge, strong programming skills and proficiency in parallel and cloud computing. | 3/12/2021 |
| 9217 | Enzo Life Sciences Farmingdale, NY Associate Manufacturing Scientist BS in Relevant Scientific Discipline Exp: 1-3 Years |
This position is responsible for the planning, implementation, and maintenance of manufacturing methods, processes, and operations for current and new product lines, as well as contributing to the improvement of production capabilities. The Associate Manufacturing Scientist is also responsible for understanding product specifications, troubleshooting technical problems, and implementing process improvements. | 3/12/2021 |
| 9218 | Enzo Life Sciences Farmingdale, NY Technologist BS in Clinical Lab Science, Medical Technology, or Related Exp: 1+ Years |
Responsibilities: The technologist will perform qualitiative and quantitative tests and examinations using various analyzers and/or manual methods. Assist in peforming established quality assurance procedures (quality control testing, instrument function checks and calibrations). Mainatains appropriate documentation and reports irregularities. | 3/12/2021 |
| 9219 | Enzo Life Sciences Farmingdale, NY Production Associate I BS in Biology or Related Exp: 0-2+ Years |
This position is responsible for the timely and efficient scheduling and packaging of standard and custom products, and for providing support to other areas of manufacturing to ensure timely product delivery. | 3/12/2021 |
| 9220 | EQRx Cambridge, MA Clinical Data Scientist MS in Biostatistics, Epidemiology, Health Economics, Public Health, or Computative Biology Exp: 1-3 Years |
You will conduct analyses using various disparate types of healthcare data (e.g., clinical trial data, insurance claims data, Electronic Health Record (EHR) data, etc.). You will explore these data with a critical eye and transform these data into meaningful insights, creating outputs that may be used for publication, regulatory submissions, internal decision-making, market tracking, or other uses. Working closely with the other members of the Clinical Computational Sciences team, you will be encouraged to use new and emerging data sources and technologies to drive innovation and to conduct analyses at scale. | 3/12/2021 |
| 9221 | ERT Clinical Philadelphia, PA Cardiac Safety Specialist BS in Life Sciences Discipline Exp: 0+ Years |
As a Cardiac Safety Specialist you will receive the full training necessary to acquire ECGs from Holter recordings (extraction); digitize PNG images to XML files; record interval duration measurements on paper ECGs (EXPeRT environments) or digital ECGs (Overread Client or EXPeRT environments); Holter arrhythmia analysis; review ECGs for safety/alert findings. | 3/12/2021 |
| 9222 | ERT Clinical Philadelphia, PA Prototype Design Specialist BS in Relevant Discipline Exp: 0+ Years |
Responsibilities: Collaborate with product management and engineering to define and implement innovative solutions for the product direction, visuals and experience. Execute all visual design stages from concept to prototype. Create simple and intuitive experiences by distilling product requirements and user goals into sketches, wireframes, and prototypes and continuously iterating to meet customer needs. Designing original pieces, including illustrations and infographics and presentation decks Contribute to and help evolve ERT’s design system and individually contribute on an array of projects that use the design system. | 3/12/2021 |
| 9223 | ERT Clinical Philadelphia/Pittsburgh/Cleveland, PA Quality Assurance Auditor BS in Health or Life Science Discipline Exp: 0+ Years |
ERT is looking to hire a QA Auditor to perform quality audits and assessments of ERT’s procedures and data to assure compliance and quality of the services and systems developed and implemented by ERT. | 3/12/2021 |
| 9224 | Exelixis Alameda, CA Assistant Research Scientist II (Compound Repository) MS in Relevant Scientific Discipline Exp: 0-2 Years |
The successful candidate will be joining the Compound Repository team to support small molecule compound characterization in Exelixis research programs. The candidate will be responsible for executing daily compound processing and deliveries for HTS assay screens. This job will require the candidate to have excellent organization, communication, and teamwork skills, as well as flexibility and versatility, to meet tight deadlines in a dynamic, fast-moving environment. | 3/12/2021 |
| 9225 | Exelixis Alameda, CA Clinical Supplies Manager MS in Relevant Discipline Exp: 1+ Years |
The Clinical Supplies Manager will oversee all aspects of clinical supply management including packaging, labeling, monitor inventory levels, and distribution by interacting with internal and external supply partners/vendors to ensure supply of IMP are sufficient at depots and clinical sites. | 3/12/2021 |
| 9226 | Exelixis Alameda, CA Market Access Operations Analyst BS in Public Healthcare, Healthcare Administration, Data Management, or Related Exp: 1+ Years |
The Market Access Operations Analyst will be responsible for: Providing operational and analytical support for commercial and trade rebates. Assisting in processing managed care and other trade related invoices. Assisting in tracking rebates against requisition limits. Supporting the regular reporting and analysis activities for account manager and leadership review. Maintaining documentation of contracts, requisitions, and payments in support of various audit and other reporting requirements. | 3/12/2021 |
| 9227 | BioPharmGuy Anytown, US Contract Data Work some college Exp: 0 yrs |
We are looking for people to do some data confirmation tasks. Mostly checking Google, Company Websites & LinkedIn to confirm the info we have is accurate. Must be able to accept payment via PayPal. If interested, send a message through the contact form. Thanks! | 3/7/2021 |
| 9228 | Dropworks Boulder, CO Research Associate BS or Equivalent in Biological Sciences or Related Exp: 1-5 Years |
Dropworks is seeking a Research Associate with experience in PCR-based assays to join their team for the development of an exciting new digital PCR platform. This position will be responsible for designing, executing and analyzing experiments on their digital PCR system to aid in assay and product development. Ideal candidates will display an inquisitive nature, good time management and have a strong attention to detail. This position will require clear communication and frequent interaction with cross-functional team members, including significant exposure to an engineering environment. | 3/5/2021 |
| 9229 | Dropworks Boulder, CO Material Handler BS in Relevant Discipline Exp: 0+ Years |
Dropbox is seeking a motivated, reliable employee to manage their factory’s incoming and stored inventory to directly service the production line in the factory. This position is ideal for someone with experience managing inventory and working in a manufacturing or warehouse setting, looking to eventually move into a warehouse manager type role. | 3/5/2021 |
| 9230 | Dr. Reddys Shreveport, LA Associate QC/Sr. Chemist BS in Chemistry or Biochemistry Exp: 0-5 Years |
Responsibilities: Conducts, with minimal supervision, basic and complex analyses of raw material, release and/or stability samples following approved methods, standard operating procedures and other instructional documentation. Prepares accurate and complete records of the work performed. Basic understanding of the requirements of the USP and GMP requirements as applied to the wet chemistry testing of active pharmaceutical ingredients and raw materials. Sets up and operates more complex laboratory equipment such as dissolution apparatus, HPLC and GC inclusive of any computerized software required for the operation of the equipment or analysis of results. Makes recommendations with respect to the cause and resolution of equipment issues or malfunctions. Demonstrates an understanding of the factors impacting analytical test results and makes recommendations with respect to root cause, corrective action and actions to prevent recurrence (i.e. CAPA) inclusive of changes to methods and procedures. | 3/5/2021 |
| 9231 | Dyne Therapeutics Waltham , MA Research Associate Scientist, Platform Development BS in Biology, Chemistry, or Biochemistry Exp: 1-3 Years |
Dyne is seeking a talented and highly motivated Research Associate Scientist in analytical chemistry/biochemistry to help generate and advance their therapeutics research and support their drug discovery programs. In this role the candidate will be responsible for developing and running analytical assays to characterize a variety of research materials. S/He will collaborate closely with the platform group and colleagues across research to characterize therapeutic materials and will also have an opportunity to help establish and contribute to the operations of Dyne laboratories. | 3/5/2021 |
| 9232 | DynoSense San Jose, CA Software Engineer BS in Computer Science, Engineering, or Related Exp: 0+ Years |
Responsibilities: Coding, implementing, and documenting software programs and applications. Consulting with managerial, engineering, and technical personnel to clarify program intent, identify problems, and suggest changes. Compiling and writing documentation of program development and subsequent revisions, inserting comments in the coded instructions so others can understand the program. Applying code libraries, framework to simplify the coding. Ensuring that the program is aligned to the framework architecture and is consistent with overall standards across different components to increase maintainability and code efficiency. Profiling and modifying software programs to improve performance. Developing iOS mobile application for sensor information capture and display, to-do list module, goal list setup and display, symptom checker and display analyzing results, medication log, importing and syncing with 3rd party device information, profile module setup. | 3/5/2021 |
| 9233 | DynoSense San Jose, CA QA Engineer BS in Computer Science, Engineering, or Related Exp: 0-2 Years |
Responsibilities: Estimate, plan, and coordinate testing activities. Develop test plan, test cases, test scenarios based on Users Stories and product’s design description to meet business requirements and technical specifications. Perform ad hoc, functional, integration, and regression testing. Identify software defects and submit problem reports via bug-tracking system. Perform regression testing on fixed issues. | 3/5/2021 |
| 9234 | Eurofins Los Angeles, CA Matallographer BS in Metallurgy or Materials Science Exp: 0+ Years |
Responsibilities: Metallographic sample preparation includes cutting, mounting, identifying, polishing and etching specimens in accordance with appropriate procedures. Perform hardness and microhardness testing. Organize work for efficient execution according to procedures. Maintain flow through met prep and metallography to meet customer needs and promote efficiency. Must have interest in learning new techniques to work of special metals. | 3/5/2021 |
| 9235 | Eurofins East Windsor, NJ Semiconductor Prep Technician BS in Relevant Discipline Exp: 1+ Years |
This position will be responsible for supporting SIMS Scientist activities by preparing samples and equipment for analyses, including but not limited to, mounting, machining, and polishing techniques | 3/5/2021 |
| 9236 | Eurofins Milpitas, CA SEM Materials Science Technician/Analyst BS in Engineering or Physical Science Discipline Exp: 0+ Years |
Job functions include Scanning Electron Microscopy (SEM) Imaging, sample prep cross-sectioning, microcleaving. The individual will work closely with tool vendors to understand tool performance and develop new techniques to improve throughput, perform basic tool maintenance and calibration, communicate with customers and prepare PowerPoint reports. The work environment is fast-paced with firm deadlines. The successful candidate will work as a part of a team and be expected to rapidly gain a working knowledge of many analytical techniques. | 3/5/2021 |
| 9237 | Editas Medicine Cambridge, MA Research Associate II, Cell Process Development MS in Biological Science, Biotechnology, Pharmaceutical Sciences, or Biomedical Engineering Exp: 0-2 Years |
Responsibilities: Work collaboratively with Research to transfer cell-based processes into PD. Perform or assist in process development and optimization surrounding cell culture and scale-up of processes. Assist in collaborations with AD to generate data to support formulation studies, stability studies, and characterization of drug substance and/or drug product. Document all experimental work, supporting information, and data in an electronic lab notebook (eLN) in a timely manner. Perform or assist in the compilation of data, authoring, and review of batch records, technical reports, and supporting procedures. Support generation of reference standards, lead stability samples, forced stability samples, toxicology lots, non-human use (NHU) engineering run lots, and clinical manufacturing run lots, as appropriate. | 3/5/2021 |
| 9238 | Element Biosciences San Diego, CA Scientific Software Developer MS in Computer Science, Bioinformatics, Computational Biology, Mathematics, or Related Exp: 0+ Years |
This position seeks an exceptional candidate with a deep understanding of algorithms and strong scientific software development skills. The work environment provides a variety of projects with an opportunity to work on product design and green-field analysis infrastructure. You will design and implement innovative algorithms for the analysis of high throughput data. You will work as part of a cross-disciplinary team on the foundational aspects of an exciting, new technology. Your work will directly drive technology improvement and become a part of the customer-facing offering. | 3/5/2021 |
| 9239 | Element Biosciences San Diego, CA Research Associate, Surface Chemistry BS in Chemistry, Materials Science, Biochemistry, Bioengineering, Physics, or Related Exp: 1+ Years |
Element is looking for a scientifically oriented, creative, and highly talented individual with a curious mind and a great desire to learn new techniques and tackle new areas of study to join their interdisciplinary research team. You will be helping in experiment design, materials synthesis and characterization including testing surface properties, and exploration of surface coating process at the fundamental level. The preferred candidate will have scientific research lab experience, demonstrated by any combination of prior curricular, extracurricular undergraduate research lab work, scientific paper, poster, or presentations. | 3/5/2021 |
| 9240 | Element Biosciences San Diego, CA Assay Scientist I, Biochemistry MS in Chemistry, Biochemistry, Molecular Biology, Bioengineering, or Related Exp: 1+ Years |
Element is seeking a scientist contributor to work with cross-functional departments to understand enzyme requirements and build assays and characterization tools to determine if enzymes meet specifications. This position requires the technical expertise and drive to work independently and in combination with a small team to deliver understanding and mitigations to enzyme performance and stability. Characterization methods will employ both solution-based and surface interaction-based studies. The Assay Scientist develops advanced methods/techniques for testing and evaluation and will provide project leadership, technical consultation, work direction, and training to junior personnel. Must be comfortable working without appreciable direction on assigned projects/programs and assisting in determining objectives of assignments. | 3/5/2021 |
| 9241 | Element Biosciences San Diego, CA Research Associate, Protein Purification BS/MS in Biology, Chemistry, Biochemistry, Molecular Biology, Bioengineering, Chemical Engineering, or Equivalent Exp: 1+ Years |
Responsibilities: Perform protein purification using AKTA-based column chromatography and high-throughput automation. Transformation of target clones and expansion of E. coli bacterial cultures from colony to liter scale. Perform SDS-PAGE and UV or colorimetric protein concentration measurements. Support protein engineering screening assays and/or quality control as needed. Manage clone and purified protein storage and archiving. Maintain laboratory equipment and reagents stocks. Maintain good documentation practices including organization of data and completion of batch records.Responsibilities: Perform protein purification using AKTA-based column chromatography and high-throughput automation. Transformation of target clones and expansion of E. coli bacterial cultures from colony to liter scale. Perform SDS-PAGE and UV or colorimetric protein concentration measurements. Support protein engineering screening assays and/or quality control as needed. Manage clone and purified protein storage and archiving. Maintain laboratory equipment and reagents stocks. Maintain good documentation practices including organization of data and completion of batch records. | 3/5/2021 |
| 9242 | Element Biosciences San Diego, CA Associate Scientist, Sequencing Biochemistry and Reagent Development BS/MS in Chemistry, Biochemistry, Bioengineering, or Equivalent Exp: 1+ Years |
Responsibilities: Design and conduct hypothesis driven experiments. Implement and maintain process workflows and good work practices. Support the optimization of reagents for our new NGS technologies. Write and version SOPs and work instructions. Collaborate closely with upstream research teams and downstream ops/manufacturing teams as products evolve. Analyze data, record, and present results. | 3/5/2021 |
| 9243 | Element Biosciences San Diego, CA Research Associate, Systems Integration MS in Relevant Scientific Discipline Exp: 1+ Years |
The Systems Integration group is seeking a research associate to assist with ongoing R&D efforts testing product readiness for market. Ideal candidates will work under the direction of scientists to run and maintain instruments and assist in the integration of hardware and chemical components. Candidates are expected to be eager to learn and familiar with common molecular biology laboratory techniques. With mentoring, the candidate will be able to develop and optimize methods/techniques for testing and the evaluation of cutting-edge genomics technologies. | 3/5/2021 |
| 9244 | Elite Pharma Northvale , NJ Raw Material Chemist BS in Chemistry or Related Exp: 0+ Years |
The primary responsibility is to perform routine release testing of raw materials (Active ingredient, excipients, colors,) and packaging materials in accordance with established procedures (in-house, Pharmacopeial, vendor procedures) | 3/5/2021 |
| 9245 | Merck KGaA Carlsbad, CA Quality Analyst I, Microbiology BS in Chemistry, Biology, or Similar Life Sciences Discipline Exp: 0+ Years |
As a Quality Analyst 1 in the Quality Control Environmental Monitoring group, you will support the site by testing the quality of the cleanroom manufacturing environment and that SAFC Carlsbad adheres to strict regulatory and ISO requirements. Monitoring activities include, but are not limited to, collecting surface, air, water and personnel samples, monitoring manufacturing processes, enumerating microbial plates, data entry, trend analysis, reporting deviations and nonconformances, and investigation support. The role will entail operating in a fast-paced, highly dynamic environment in collaboration with other departments as well as external stakeholders. This role will support the daily operations of the Environmental Monitoring Group, collect samples, process samples, complete documentation, enter data, and review data for Environmental monitoring. | 3/5/2021 |
| 9246 | Merck KGaA St. Louis, MO QC Logistics Technician 3 BS in Life or Physical Sciences Exp: 0+ Years |
Responsibilities: Logistics functions include material movements in SAP, bulk sampling, analytical weigh-ups, delivery to labs, sample retain management, ship materials to outside labs, etc. Weigh chemicals with correct amount of precision, as dictated by the type of assay and quantity of product required. Contribute to support functions of the lab (e.g., maintain equipment, restock lab, waste disposal, material deliveries, etc.). Complete the volume of work required to achieve group/departmental goals and meet deadlines. Communicate the status of operations and bring deviations to the attention of the Supervisor. Provide complete and accurate records consistent with quality guidelines. Ensure all applicable logbooks have been filled out completely as required by current procedures. Interact with other departments as needed. | 3/5/2021 |
| 9247 | Merck KGaA Milwaukee, WI Associate Production Scientist BS in Chemical Engineering, Chemistry, Biology, or Related Exp: 0+ Years |
The Associate Production Scientist will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 3/5/2021 |
| 9248 | Merck KGaA Burlington, MA Technical Service Specialist I BS in Biology, Biochemistry, Chemistry, Engineering, or Related Exp: 0+ Years |
Responsibilities: Handle multiple projects/responsibilities simultaneously. Maintain composure in challenging situations. Portray a dedicated commitment to fulfill customers’ needs and solve problems. Support our customers with their product and application inquires by providing technical information, troubleshooting, and recommending solutions. Manage concerns related to product quality by working with quality groups. Interact regularly with cross-functional teams within the organization. Assist in technical training programs. | 3/5/2021 |
| 9249 | Merck KGaA Kankakee, IL Process Engineer BS in Chemistry, Biochemistry, Biology, Chemical Engineering, or Related Exp: 1+ Years |
In this role, you will assist the research and troubleshooting of defective products in order to identify potential root cause failure. You will identify key process parameters, define their impact on product quality, and subsequently develop and modify formulations, methods and controls to meet quality specifications. Your processing insights will be used to recommend and implement improvements, modifications, or additions to document work. Additionally, you will support the maintenance of production records and documents. As you grow in your position, manufacturing supervisory duties may be required. | 3/5/2021 |
| 9250 | Merck KGaA Danvers, MA Development Engineer BS in Computer Science or Engineering Discipline Exp: 0-3 Months |
Responsibilities: Gathering requirements from internal customers for specific applications. Organizing requirements into appropriate flowcharts and writing Software Specifications. Developing the software using appropriate tools and programming skills pertinent to the application. Some applications may be in Excel using Excel’s VBA platform, others may be written using C#.NET, SQL or other languages as appropriate. Modification to existing software projects. Software testing, debugging, and validation as required. Writing user guides, test scripts, test protocols and final reports as required. | 3/5/2021 |
| 9251 | Merck KGaA Verona, MO Associate Production Scientist BS in Chemistry, Biochemistry, Biology, Chemical Engineering, or Related Exp: 0+ Years |
Position primarily involves the safe and efficient manufacturing of API’s according to cGMP requirements. The role of Production Scientist, Associate is primarily focused on performing required production operations to support the end users and patients of the compounds produced at MilliporeSigma. These responsibilities include but are not limited to executing existing production procedures, updating ancillary documents, and maintaining the safety and quality of the manufacturing environment. | 3/5/2021 |
| 9252 | Emmaus Medical Torrance, CA Research Assistant BS/MS in Biology or Related Exp: 1-2 Years |
The Research Assistant will assist in the development and characterization of stem cell, cell sheet research and anti-cancer drug for the treatment of rare diseases. This individual will work under the supervision of the Principal Investigator and will have an excellent opportunity to gain life sciences lab experience in a stateof-the–art research environment. This position is primarily located in the laboratory with occasional office work required. | 3/5/2021 |
| 9253 | Empirico San Diego, CA Bioinformatics Engineer, Translational Genetics BS/MS in Bioinformatics or Related Exp: 0-3 Years |
Your responsibilities will primarily consist of performing analyses and building robust computational pipelines and tools critical to Empirico’s drug discovery efforts. | 3/5/2021 |
| 9254 | Empirico Madison, WI Laboratory Assistant BS in Molecular Biology or Related Exp: 0+ Years |
Empirico, a human genetics-focused biotechnology company, is looking for a laboratory assistant to help with routine laboratory operations. This is an excellent opportunity to gain hands-on experience working at a highly innovative biotechnology company and with experienced scientists that have a passion for finding novel approaches toward the treatment and prevention of disease | 3/5/2021 |
| 9255 | Enanta Pharma Watertown, MA Associate Scientist, Drug Metabolism & Pharmacokinetics BS in Biology or Related Exp: 0+ Years |
The Associate Scientist will work with an experienced Ph. D. scientist to conduct drug permeability and liver / intestine / lung / kidney transporter studies in support of Enanta drug discovery programs. She/he will be an integral member of Enanta’s highly collaborative Pharmacology and DMPK/Bioanalysis Department focused on the discovery of novel therapeutics against liver and viral diseases including nonalcoholic steatohepatitis (NASH), primary biliary cholangitis (PBC), respiratory syncytial virus (RSV), and hepatitis B virus (HBV), etc. | 3/5/2021 |
| 9256 | Enanta Pharma Watertown, MA Contracts Coordinator BS in Relevant Discipline Exp: 0+ Years |
The Contracts Coordinator will be responsible for assisting the Legal team with contracts and related responsibilities. This is an entry level position reporting to the Senior Director, Contracts Management in the Legal Department. The Contract Coordinator will work with all members of the Legal team, as well as staff across the company. | 3/5/2021 |
| 9257 | Enanta Pharma Watertown, MA Scientist, Analytical Method Development BS/MS in Relevant Discipline Exp: 0+ Years |
The Scientist/Senior Scientist, Analytical Method Development will be responsible for all aspects of analytical development including characterization for drug substances and drug products. This position is responsible for performing analytical method development and support for drug substance development, formulation development, manufacturing, stability, characterization and control. | 3/5/2021 |
| 9258 | Cytovance Biologics Oklahoma City, OK Process Development Associate I BS in Biochemistry, Microbiology, Biology, Chemistry, or Chemical Engineering Exp: 0-3 Years |
The Process Development Associate I conducts laboratory experiments in a productive manner with consistent quality and timely outputs, under supervision. Responsibilities: Stays current with all training requirements. Follows procedures reliably and consistently. Sets up experiments, monitors, and acquires analytical data. Keeps detailed, accurate and clearly written records in accordance with GDPs. Establishes good working relationships with peers and other colleagues. Displays a positive attitude and good change readiness. Independently supports good lab hygiene. Recognizes and troubleshoots outcomes that are not aligned with expectations and seeks guidance as appropriate. | 2/26/2021 |
| 9259 | Dascena Oakland , CA Senior Data Science Manager BS/MS in Data Science, Bioinformatics, Statistics, or Related Exp: 0+ Years |
As a Clinical Data Science Manager at Dascena, you will lead a small, focused team of data scientists to conduct research and development of next-generation clinical machine learning algorithms. You will work closely with scientific writers and a data engineering team to deliver the data science results for research papers, regulatory submissions, and funding proposals. You will collaborate with business stakeholders to deploy machine-learning algorithms into real-life clinical settings. | 2/26/2021 |
| 9260 | DayZero Diagnostics Boston, MA Data Scientist Associate BS/MS in Computer Science, Machine Learning, Computational Biology, Bioinformatics, or Related Exp: 0+ Years |
This Data Scientist Associate position is on the data science team at DZD, which is responsible for training machine learning models to predict antimicrobial resistance from genomic sequencing data and generally supporting data analytics across the company. The Data Science Associate can expect to be involved in model R&D (featurization, model specification and training, performance analysis, etc), as well as ad hoc analytics work and preparing models for deployment into production. Much of the work will involve interactions with software engineering and computational biology teams, and being able to work both collaboratively and independently are key. | 2/26/2021 |
| 9261 | DayZero Diagnostics Boston, MA Laboratory Research Assocaiate BS in Molecular Biology, Biochemistry, or Microbiology Exp: 0+ Years |
Responsibilities: Perform and assist with sample processing toward diagnostic workflows. Strictly follow all lab procedures for specimen handling, processing, and reporting. Maintain meticulous documentation of experimental outcomes and observations. Work closely with Research Scientists and Associates, and maintain close communication with direct supervisor. Repetitive workflows are a frequent occurrence. | 2/26/2021 |
| 9262 | DayZero Diagnostics Boston, MA Laboratory Research Assocaiate II R&D MS in Molecular Biology, Biochemistry, or Microbiology Exp: 1 Year |
Responsibilities: Perform and assist with sample processing toward diagnostic workflows. Design and carry out research and development experiments in collaboration with DZD lab team. Analyze and present experimental data for the R&D team. Maintain meticulous documentation of experimental outcomes and observations. Work closely with Research Scientists and Associates, and maintain close communication with direct supervisor. Repetitive workflows are a frequent occurrence. | 2/26/2021 |
| 9263 | Decibel Therapeutics Boston, MA Research Associate BS/MS in Biological Sciences or Related Exp: 1+ Years |
Decibel is currently looking for a motivated research associate to join their ex vivo tissue culture team. The successful candidate will work on cutting-edge gene therapy programs. His/her work will contribute to multiple early stage discovery efforts and create the bedrock of potential treatment programs. | 2/26/2021 |
| 9264 | DeepBiome Therapeutics Cambridge, MA Machine Learning Scientist BS/MS in Computational Science or Related Exp: 0+ Years |
Responsibilities: Build and reinforce the computational framework for processing various metagenomics projects with indications in human health. Work alongside bioinformaticians, computational biologists, engineers, and biologists in a highly collaborative environment. Learn existing biological databases and how we can leverage them into our platform. Analyze, improve, and maintain relational databases. Develop and maintain high quality revision-controlled code. Build docker images for complicated tasks. | 2/26/2021 |
| 9265 | DeepBiome Therapeutics Cambridge, MA Research Associate BS/MS in Bioengineering, Molecular Biology, Synthetic Biology, Microbioloy, or Related Exp: 1-2+ Years |
DeepBiome is seeking a Research Associate/Senior Research Associate to support their proprietary drug discovery platform. The candidate will be joining DeepBiome’s synthetic biology group and working in a cross-functional project team. Responsibilities: Design, assembly, manipulation and cloning of DNA constructs for in vivo bacterial expression. Construct gene and pathway plasmid constructs using assembly methods such as: yeast homologous recombination, Gibson assembly, Golden Gate assembly. Transformation, cultivation, and cataloging a range of microbes (BSL1/BSL2 bacteria and yeast). Acquire, evaluate, and interpret scientific data in conjunction with scientists in a cross-functional team. Use of computational tools and databases (e.g. Geneious, BLAST search). Maintain a laboratory notebook with detailed notes and trackable time stamps. | 2/26/2021 |
| 9266 | Deep Genomics Toronto, ON Bioinformatician BS/MS in Computer Science, Bioinformatics, or Related Exp: 0+ Years |
Deep Genomics seeking a highly motivated bioinformatician with strong programming and scripting skills to help us advance their therapeutic programs to the next level. The successful candidate will work in a multidisciplinary team of biologists and computational scientists and take on tasks spanning analysis of experimental data, genomics data processing, and data visualization from a multitude of therapeutic programs. The ideal candidate would have a good understanding of molecular biology, human genetics, and basic statistics. | 2/26/2021 |
| 9267 | Deep Genomics Toronto, ON Laboratory Assistant BS in Life Sciences or Related Exp: 1-3 Years |
Deep Genomics is seeking a Laboratory Assistant to help their growing, fast paced team! Working closely with both their laboratory and operations teams, you will help them with day to day administrative and laboratory tasks. They are looking for a helpful, organized, and hardworking individual, with a flexible attitude to job roles. | 2/26/2021 |
| 9268 | Deep Genomics Toronto, ON Scientist - Machine Learning MS in Machine Learning or Related Exp: 0+ Years |
We are seeking a creative and experienced machine learning scientist to decipher how mutations and genetic medicines influence the molecular world of the cell. The successful candidate will develop machine learning approaches for modeling complex RNA- and protein-level outcomes based on massively parallel assays. The ideal candidate has a proven track record of publishing at top machine learning conferences (NIPS, ICML, ICLR) or has applied deep learning to genomics in a top life sciences journal. | 2/26/2021 |
| 9269 | Demetrix Berkeley, CA Associate Scientist BS in Biology, Biochemistry, Biological Engineering, or Chemical Engineering Exp: 1+ Years |
You will be part of the High Throughput Screening group at Demetrix and will facilitate a variety of high throughput pipelines related to building and testing of microbial strains. You will be part of an interdisciplinary team of scientists and engineers working to rapidly develop microbial strains to produce natural product medicines. | 2/26/2021 |
| 9270 | Demetrix Berkeley, CA Associate Scientist BS/MS in Biology, Chemical Engineering, Molecular Biology, Biochemistry, Biophysics, Cell Physiology, or Related Exp: 1-2 Years |
You will be part of the DNA Operations group at Demetrix and will facilitate a variety of high throughput pipelines related to building and testing of microbial strains. You will be part of an interdisciplinary team of scientists and engineers working to rapidly develop microbial strains to produce natural product medicines. | 2/26/2021 |
| 9271 | Dendreon Seattle, WA Medical Information Specialist - Patient Services MS in Relevant Clinical or Scientific Discipline Exp: 1-3 Years |
Reporting directly to the Vice President of Medical Affairs, the Medical Information Specialist [Patient Services] is primarily responsible for developing and providing direct medical, scientific and operational input into core medical information documents and product lot failure notifications for both healthcare professionals (HCPs) and non-HCPs (including patients and consumers), and payors. The position will be responsible for processing and documenting enquiries received by phone or email with fair and unbiased medical information through published scientific literature and confidential company data. | 2/26/2021 |
| 9272 | Dendreon Seattle, WA Scheduling Case Manager I BS in Relevant Discipline Exp: 1-2 Years |
Dendreon Patient Operations manages the creation of the production plan and execution of arm-to-arm activities supporting Provenge treatments, including but not limited to production and demand planning, logistics analysis, scheduling, and real-time product monitoring. The primary focus of this position is to schedule and monitor patients treatment schedules according to the care providers preferences in a diverse call center environment while providing an exceptional customer experience throughout the entire process. | 2/26/2021 |
| 9273 | DiaCarta Richmond, CA Manufacture Technician BS in Molecular Biology, Cell Biology, Biotechnology, or Related Exp: 1+ Years |
Responsibilities: Production of DiaCarta IVD products to meet sales demands. Manufacturing of IVD kit components and finished goods according to SOP. Preparation of bulk materials from chemical ingredients. Incoming materials verification and testing. Labeling of raw materials and finished goods. Documentation and record-keeping for tasks performed. Participate in process improvement projects. Compliance with corporate quality systems. Other on-the-job assignments indicated by management. | 2/26/2021 |
| 9274 | Dice Molecules San Francisco, CA Research Associate/Senior Research Assocaite, Chemistry MS in Chemistry Exp: 0-6 Years |
Dice Molecules is seeking an exceptional full-time lab-based synthetic chemistry Research Associate / SeniorResearch Associate to join their medicinal chemistry team. This individual will be a key contributor to the synthesis of intermediates and final compounds within the goals of developing treatments for inflammatory diseases. | 2/26/2021 |
| 9275 | Digirad Multiple Locations , U. Cardiac Stress Technician BS in Relevant Discipline Exp: 0+ Years |
The Cardiac Stress Technician will work under the direct supervision of site physician, performing various professional and administrative duties related to nuclear medicine stress testing. This includes but not limited to patient preparation, administration of exercise and pharmacological stress tests, and application of ACLS measures to patients when directed. | 2/26/2021 |
| 9276 | Digirad Multiple Locations , U. Nuclear Medicine Technologist BS/MS in Nuclear Sciences Discipline Exp: 1+ Years |
The Nuclear Medicine Technologist will work will work under the direct supervision of site physician, performing various duties related to nuclear stress testing. Performs patient care functions related to perfusion imaging and stress testing at customer sites. | 2/26/2021 |
| 9277 | Digirad Fargo, ND Manager of Quality and Regulatory Compliance MS in Relevant Discipline Exp: 0-2 Years |
The Manager of Quality & Regulatory Compliance assists the CEO with planning, organizing, executing, and maintaining continual readiness for Joint Commission surveys, OSHA, ACR Accreditation, Mammography FDA inspections, ISO 9001, and Canada Health regulations. This includes but is not limited to staying abreast of appropriate regulatory requirements and standards, coordinating all communication with all Regulatory organizations, and dispersing relative information to the appropriate DMS Health Technologies personnel. | 2/26/2021 |
| 9278 | DiscGenics Salt Lake City, UT Raw Materials Research Associate BS in Biological, Biochemical, or Chemistry Related Field Exp: 1-5 Years |
DiscGenics is seeking a research associate who can support the raw material team by performing a variety of cell culture and chemical test methods as well as assisting with donor procurement. This is a laboratory position that will provide experience with cell culture and cell characterization methods. The ideal candidate will be driven and enthusiastic about our mission to aid patients with disc degeneration and have some experience with cell culture, cell based assays and chemical analysis. This role is intended to grow into a scientist position with increased independence and responsibilities. | 2/26/2021 |
| 9279 | Eurofins Fremont, CA Associate Product Manager BS in Life Sciences or Related Exp: 1 Year |
Responsibilities: Perform business and market analysis of the product line. Implement the product strategy based on market research and analysis, competitive intelligence, industry trends, voice of customer (VOC) to meet revenue targets and goals, define core positioning and messaging, and pricing strategies. Conducts portfolio analysis and monitor revenues and wins/losses for the assigned product lines. Collaborates with internal stakeholders to support the product lifecycle management of the portfolio based on market dynamics, competitive pressures, and internal strategies. Implement product and application launch activities including product positioning, promotional and pricing strategies, training and working with cross-functional teams (e.g. market development, R&D, sales, and tactical marketing communications team, etc.). | 2/26/2021 |
| 9280 | Disterk North Brunswick, NJ Field Validation Specialist BS in Chemistry, Physics, Biology, or Chemical Engineering Exp: 1-2 Years |
Distek, Inc., a rapidly growing leader in the scientific instrumentation field is currently seeking a Validation Specialist in the New Jersey area to perform Instrumentation Services at customer sites. They will be responsible for validation, calibration, testing, installation, and repair or laboratory instruments. | 2/26/2021 |
| 9281 | Diversigen/Orasure Technologies Bethlehem, PA Formulations Specialist BS in Chemistry, Biochemistry, or Equivalent Exp: 1-3 Years |
Manufacture chemical formulations necessary for production of finished goods in accordance with current batch production records (BPR). | 2/26/2021 |
| 9282 | Diversigen/DNA Genotek Ottowa, ON Manufacturing Engineer BS/MS in an Engineering or Science Discipline Exp: 1-2 Years |
The Manufacturing Engineer I is responsible for supporting projects that may include new products, new equipment, process and quality improvements, process validations, and cost reductions for internal manufacturing and sustaining activities at contract manufacturers. Responsibilities also include creating and/or reviewing work instructions, Engineering Configuration Notices, BOMs, item masters and label masters as required, and completing investigations of nonconformances and any resulting CAPAs. | 2/26/2021 |
| 9283 | DNAnexus Mountain View, CA Bioinformatician MS in Bioinformatics, Computational Biology, Computer Science, or Related Biotech Field Exp: 0+ Years |
This is an exciting opportunity to join DNAnexus’ growing team. We are looking for a bioinformatician who enjoys working hands-on with other scientists, software engineers, and clients to solve informatics challenges on the UK Biobank (UKB) Research Analysis Platform (RAP) cloud platform. As a member of the Innovation team in the DNAnexus xVantage organization, you will work with industry leaders across all aspects of genomics, gaining exposure to leading genomic science and application development. | 2/26/2021 |
| 9284 | DNAnexus Mountain View, CA xVantage Care Bioinformatics Scientist BS/MS in Bioinformatics, Software Engineering, or Related Biotech Field Exp: 0+ Years |
DNAnexus is looking for a bioinformatics scientist for their xVantage Care team to directly interact with clients to help them succeed with our cloud platform and solutions, and to proactively foster client relationships. | 2/26/2021 |
| 9285 | DNAnexus Mountain View, CA Senior Clinical/Healthcare Informaticist MS in Clinical/Medical Informatics, Public Health, Epidemiology, or Related Exp: 0+ Years |
As Senior Clinical/Healthcare Informaticist on the DNAnexus xVantage team you will have an opportunity to partner closely with DNAnexus customers, working with their data from profiling to ingestion, to ensure transmission and representation to end-user facing solutions that enable their precision medicine use cases. Your work will include modeling, normalization, harmonization and integration of clinical/healthcare data from multiple sources into linked clinico-genomic databases that drive scientific insight. You will partner closely with experts across the DNAnexus Data Science, Engineering, and Product teams to optimize tools and processes for clinical data pre-processing and ingestion into DNAnexus data frameworks. | 2/26/2021 |
| 9286 | DNAnexus Mountain View, CA Software Engineer: Bioinformatics Applications and Developer Tools BS/MS in Computational Science or Related Exp: 0+ Years |
As a software engineer of these applications, you will be responsible for creating products on the DNAnexus platform with the aim of delivering the best user and developer experience possible. You will contribute enhancements to our public library of apps and enable performance testing of these tools to make them highly available, scalable, fault tolerant and responsive. You will also be contributing to compilers for running workflows on DNAnexus that are written in open languages such as WDL, CWL and Nextflow. To build these tools you will work closely with scientists and bioinformaticians within the company. | 2/26/2021 |
| 9287 | DNAnexus Mountain View, CA Technical Content Developer BS/MS in Technical Writing, Biology, Computer Science, or other STEM Field Exp: 1-4 Years |
As the technical content developer, you will be joining a growing engineering and product management organization to produce content that translates complex technical products and features into easily consumable documentation, training materials and marketing content. You will be responsible for clearly and concisely communicating new and existing features of the DNAnexus platform for their user base of scientists, developers and researchers. You will help build out their onboarding content to ensure that users are successful on our platform. You will write documentation, user emails, newsletters content, and technical marketing content. | 2/26/2021 |
| 9288 | Covaris Woburn, MA Laboratory Maintenance Technician BS in Life Sciences or Related Exp: 0+ Years |
Covaris is seeking a dedicated individual who will be responsible of supporting day-to-day R&D laboratory operations. The candidate will be joining a dynamic group with a strong Team spirit. Main responsibilities will be maintenance of a functional, clean and safe laboratory. This includes equipment oversight following work instructions, organization of reagents and consumables including freezers and cold room. Opportunity to grow into a laboratory manager role. | 2/19/2021 |
| 9289 | Contract Pharmacal Corp Hauppage, NY Chemist; QC Stability BS in Chemistry Exp: 1+ Years |
Responsibilities: Perform UPLC, HPLC, GC, UV-vis, FTIR, ICP, TOC and wet chemistry testing. Proficient in various UPLC and HPLC software programs, such as Empower and EZ-Chrom. Assist in writing SOPs and Test Procedures following good documentation practice per company's SOP and cGMP regulations. Assist in OOS investigations. Perform routine laboratory chemical analysis on finished product, stability and/or raw material, also involved in performing Cleaning, Method and Process validation. Troubleshoot basic instrument problems with supervision. Provide well-written, accurate and timely reports. Perform all work using appropriate safety measures and following company Chemical Hygiene Plan. Strictly adhere to all applicable safety and standards guidelines such as SOP, cGMP, DEA regulations and/or MSDS. | 2/19/2021 |
| 9290 | Contract Pharmacal Corp Hauppage, NY Scientist I; AR&D BS/MS in Chemistry or Analytical Chemistry Exp: 1-2 Years |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. Responsibilities: Knowledge of USP and FDA requirements. Design and conduct full analysis of Dietary Supplements and Active Pharmaceutical Ingredients (API) products and their impurities. Conduct assay, content uniformity, dissolution, in-process blend, and blend uniformity of newly developed and stability samples in support of formulation and process development. Prepare result documentation for department and general review. Conduct Performance Qualification (PQ) on various instruments. Effectively communicate information in concise reports. | 2/19/2021 |
| 9291 | Contract Pharmacal Corp Hauppage, NY Administrative Assistant, Regulatory Affairs BS in Science or Compliance Exp: 0+ Years |
Responsible for supporting the Regulatory Affairs department in its efforts to remain in compliance with the regulations of all intended market territories; for preparing and maintaining Regulatory Affairs files; and, for other administrative roles/tasks. | 2/19/2021 |
| 9292 | Contract Pharmacal Corp Hauppage, NY Chemist I; QC Raw Materials BS in Chemistry Exp: 1+ Years |
Responsibilities: Perform UPLC, HPLC, GC, UV-vis, FTIR, ICP, TOC and wet chemistry testing. Proficient in various UPLC and HPLC software programs, such as Empower and EZ-Chrom. Assist in writing SOPs and Test Procedures following good documentation practice per company's SOP and cGMP regulations. Assist in OOS investigations. Perform routine laboratory chemical analysis on finished product, stability and/or raw material, also involved in performing Cleaning, Method and Process validation. Troubleshoot basic instrument problems with supervision. Provide well-written, accurate and timely reports. Perform all work using appropriate safety measures and following company Chemical Hygiene Plan. | 2/19/2021 |
| 9293 | Contract Pharmacal Corp Hauppage, NY Equipment Specialsit, Project Management BS in Manufacturing, Engineering, or Related Exp: 1-2 Years |
Assist management in an administrative, project management capacity with various aspects of operations enhancement with a focus on equipment purchases/upgrades focusing on manufacturing, packaging, ERP, facilities, developmental activities, and strategic projects to support the growth of the organization. | 2/19/2021 |
| 9294 | Contract Pharmacal Corp Hauppage, NY Coordinator; QA Manufacturing BS in Relevant Discipline Exp: 1+ Years |
Responsibilities: Maintain communication with QA Validation and PM Department to ensure that all requirements for validated products, with respect to manufacturing operations, are accurate, current, and complete. Ensure that the Job request list, conveys accurate and on-time issuance of production and non-commercial batches. Ensure Administrative Assistant work regarding batch issuance and all special instructions have been met. Request issuance of batches with related labels (bulk and IP). Updating production board accordingly. Perform check of all issued batches. Coordinate with Admin, IP batch folders for deduction, posting and filing for various stages. | 2/19/2021 |
| 9295 | Contract Pharmacal Corp Hauppage, NY Administrative Assistant; QA Compliance BS in Science or Compliance Exp: 0+ Years |
The Administrative Assistant of QA Compliance has primary responsibility for supporting the administration of computer programs for ERP and QMS. Additionally, maintaining a variety of QA compliance-related initiatives. | 2/19/2021 |
| 9296 | CromSource Remote, N/ Clinical Research Associate II BS in Scientific or Medical Discipline Exp: 0+ Years |
Responsibilities: Assists in the selection of sites, site evaluation visits, initiation visits and ensuring follow up by obtaining the pre-study documentation to ensure good start-up of the investigation sites. Performs training of site staff in all study procedures in order to ensure protocol/ICHGCP compliance. Conducts and reports periodic monitoring visits in the field and reviews at each visit accuracy, eligibility, completeness and quality of Case Report Form (CRF) in compliance with the protocol, SOP's and ICH-GCP requirements in order to ensure data integrity and subject safety. Adapts and translates Patient Information Leaflets and Informed Consent Forms. Cooperates with the site staff for ensuring a proper reporting from the site of the safety issues (adverse events and adverse reaction such as AEs/SAEs, SUSARs, etc.) and their follow up, guaranteeing timely and appropriate handling of safety issues. | 2/19/2021 |
| 9297 | CryoLife Kennesaw, GA DQA Analyst BS in Biological Sciences Exp: 0+ Years |
Responsibilities: Ensure that all donors accepted and processed at CryoLife are properly identified, controlled, and meet all required quality specifications and regulatory standards prior to release for distribution. Provide support to Account Managers and facilitate obtaining donor chart information to accurately complete donor chart reviews. Organize donor chart information and all charting follow-up to meet required chart review targets and workflow. Maintain accurate pending chart information lists and pending additional information. | 2/19/2021 |
| 9298 | CryoLife Kennesaw, GA Quality Assurance Specialist I BS in Life Sciences or Related Exp: 1+ Years |
Establish and maintain Quality Systems that comply with regulations and standards. Review all records associated with the processing of human tissue and production of medical device products. Reduce waste and variability in processes. | 2/19/2021 |
| 9299 | CSBio Menlo Park, CA Analyst, Quality Control MS in Chemistry, Biochemistry, or Biology Exp: 0+ Years |
Responsibilities: Conduct sample analysis using various analytical techniques, including HPLC, UPLC, GC, KF, FT-IR, TLC, and LC-MS, GC-MS. Preparation of laboratory reagents and samples; operation of instruments; data analysis; preparation of analytical reports; notebook documentation. Support of various stability study protocols and execution of study tests. Contribute to the overall operations of the QC lab, including supplies inventory, lab safety, team meetings, responding to customer needs, etc. Perform LC/MS for compound characterization and identification with supervision. Maintain cGMP compliance in the laboratory. | 2/19/2021 |
| 9300 | CSL St. Paul, MN Quality Specialist BS in Biological Sciences Exp: 1+ Years |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 2/19/2021 |
| 9301 | CSL Holly Springs, NC Associate I/II/III, Manufacturing (Downstream) BS in Science or Engineering Exp: 1+ Years |
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (be trained in) the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant, efficient, and cost effective manner. | 2/19/2021 |
| 9302 | CSL Holly Springs, NC Associate I/II/III, Manufacturing (Fill Finish Expansion) BS in Science or Engineering Exp: 1+ Years |
Responsibilities: Conducts all assigned activities in a safe and cGMP compliant manner. Tasks will include, but are not limited to: Cleaning, preparing, and sterilizing production equipment, cleaning and disinfecting production rooms, assembly, set-up, and disassembly of production equipment, executing process steps according to defined SOPs and BPRs, documenting activities in accordance with cGMPs, and handling biologically and chemically hazardous goods. | 2/19/2021 |
| 9303 | CSL Holly Springs, NC Specialist I/II/III, QA (Front Line) BS in Relevant Discipline Exp: 1+ Years |
The Front Line Quality Assurance Specialist will provide on the floor support to manufacturing (bulk, sterile formulation/filling, and packaging), laboratories, utilities, maintenance, and logistics at the Holly Springs site. Core responsibilities of this role include quality walkthroughs on the floor, GMP record reviews and approvals, and real time triage of quality related issues. | 2/19/2021 |
| 9304 | CSL Topeka, KS Assistant Manager of Quality BS in Relevant Discipline Exp: 1+ Years |
Responsibilities: Ensure center is “inspection ready” at all times by managing adherence to Standard Operating Procedures (SOPs), compliance policies and the quality system, utilizing sound Quality principles, self-inspection learnings, non-conformity discovery and appropriate remediation. Prepare regular reports to center, area and corporate quality management as to the state of quality and systems at the center. Manage site Quality Control program including but not limited to calibrations management, monitoring of compliance to defined processes e.g. sampling, competency checks, Key Performance Indicators (KPIs), trending and analysis of KPIs, root cause and failure mode impact assessment and change management. | 2/19/2021 |
| 9305 | CSL Las Vegas, NV Quality Specialist BS in Biological Sciences Exp: 1+ Years |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 2/19/2021 |
| 9306 | CSL Syracuse, NY Clinical Lab Technician/Technologist BS in Biology, Chemistry, or Clinical Lab Sciences Exp: 3+ Months |
Responsibilities: In compliance with Standard Operating Procedures (SOPs), assists qualified donors in completing the screening process. The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the donation process, referring donors to medical staff when appropriate and performing health screening procedures such as blood pressure, pulse, weight, temperature. Performs finger stick to obtain samples of donor’s hematocrit and total protein levels. Reads and documents hematocrit and total protein results. Upon completion of the appropriate training, may educate new donors on the use of therapeutic products made from donated plasma. This includes explaining the screening process, the health screening tests performed, the appointment system, donation fees, center policies, proper nutrition and any other information pertinent to the donor. Ensures all donor questions are answered; timely, accurately and professionally. | 2/19/2021 |
| 9307 | Culture Biosciences San Francisco, CA Bioprocess Associate BS in Biology, Microbiology, Chemical Engineering, Biotechnology, or Related Exp: 1-2 Years |
Culture Biosciences is looking for a Bioprocess Associate to help run their cloud biomanufacturing facility. Your work will contribute to getting novel biotechnology products to market faster and more efficiently. You will have an opportunity to build new skills and learn about all aspects of their business. In particular, you will learn mammalian and microbial cell culture techniques and work with state-of-the-art robotics, software, and automation equipment. | 2/19/2021 |
| 9308 | Culture Biosciences San Francisco, CA Lab Assistant BS in Relevant Discipline Exp: 1-2 Years |
Culture Biosciences is looking for a Lab Assistant who will help keep their lab in tip-top shape, keep their lab operations moving smoothly, and assist their engineers to maintain their automated bioreactor infrastructure. You will be responsible for preparing bioreactors for sterilization, bioreactor repair, bioreactor cleaning, troubleshooting, harvesting, and shipping and receiving. | 2/19/2021 |
| 9309 | Culture Biosciences San Francisco, CA Hardware Engineer BS in Mechanical, Biomedical, Electrical, or Robotics Engineering Exp: 1+ Years |
Culture Biosciences is looking for a Hardware Engineer. Your focus will be on designing, building, installing, and testing new cloud connected bioreactors and lab automation. | 2/19/2021 |
| 9310 | Curi Bio Seattle, WA Electrical Engineer BS/MS in Electrical Engineering Exp: 0+ Years |
Curi Bio’s Hardware and Biosystems Engineering Team needs an Electrical Engineer to assist in the development and testing of state-of-the-art life science instrumentation products. The successful candidate will have in-depth knowledge of fundamental circuits concepts, data acquisition systems, and electrical design and test. | 2/19/2021 |
| 9311 | Curi Bio Seattle, WA Research Associate, Stem Cell and Pharmaceutical Assays BS in Biology, Bioengineering, or Biochemistry Exp: 1+ Years |
Curi is a rapidly growing startup company seeking a talented and motivated Research Associate to join their R&D team. A successful candidate will have extensive expertise in cell culture, knowledge of iPSC biology, and experience with standard cell biology assays. Experience in developing assays is highly desired. Knowledge of genome editing and tissue engineering techniques would be beneficial. | 2/19/2021 |
| 9312 | Curis Lexington, MA Clinical Trial Associate BS in Scientific Discipline Exp: 0-2 Years |
Curis is seeking a Clinical Trial Associate to provide support across all of Curis’ early stage clinical programs, within clinical operations. The CTA will work closely with Clinical Trial Managers to assist in the facilitation of clinical trials according to standard operating procedures. | 2/19/2021 |
| 9313 | Curium Pharma Maryland Heights, MO Quality Control Technicican BS in Life Sciences or Related Exp: 1-2 Years |
Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP's and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management/Supervision that presents potential negative impact to manufactured or marketed product. May supervise the work of others and coordinate instrumentation use and completion of laboratory testing. Work under limited supervision with considerable latitude for the use of initiative and independent judgment. | 2/19/2021 |
| 9314 | Curium Pharma Maryland Heights, MO Environmental Monitoring Quality Technician BS in Relevant Discipline Exp: 1-2 Years |
Perform routine environmental monitoring of aseptic processing and controlled area cleanroom environments used for pharmaceutical manufacturing. Perform assigned quality control or quality assurance activities in compliance with applicable SOP's and cGMPs. | 2/19/2021 |
| 9315 | Curium Pharma Maryland Heights, MO Microbiology Quality Control Technician II BS in Life Sciences or Related Exp: 1-2 Years |
Perform assigned quality control activities within the Microbiology Department in order to comply with applicable SOP's and cGMPs. Work under limited supervision with considerable latitude for the use of initiative and independent judgment. Must have the ability to work collaboratively, multitask, and adapt to changing priorities and schedules. | 2/19/2021 |
| 9316 | Curium Pharma Noblesville, IN Chemist II BS in Chemistry, Biochemistry, or Chemical Engineering Exp: 0+ Years |
In the role of Chemist II you will serve as part of the production team responsible for the processing of bulk radiopharmaceuticals in a highly regulated (FDA/NRC) environment. This position will be responsible for the manufacturing of radiopharmaceuticals, preparation of production materials, general production equipment maintenance, and quality control (QC) of products. | 2/19/2021 |
| 9317 | Curium Pharma Maryland Heights, MO Quality Technician, Analytical Chemistry BS in Life Sciences or Related Exp: 0-3 Years |
Perform routine Quality Control testing in accordance with Analytical methods and applicable SOP’s and cGMP’s. Perform assigned QC laboratory tasks by the required due dates. Work under limited supervision with considerable latitude for the use of initiative and independent judgment. Must have the ability to work collaboratively, multitask, and adapt to changing priorities and schedules. | 2/19/2021 |
| 9318 | Curium Pharma Maryland Heights, MO Senior Computer Systems Validation Specialist BS in Science or Engineering Exp: 0+ Years |
The Computer Systems Validation Specialist will provide validation support for computerized systems, software, and IT infrastructure that have been newly installed, upgraded, replaced and / or modified in a cGMP Manufacturing Facility. | 2/19/2021 |
| 9319 | Curium Pharma Maryland Heights, MO Manufacturing Engineer Technician II - Aseptic Suite BS in Scientific Discipline Exp: 0+ Years |
Performs all tasks associated with aseptic manufacturing of radiopharmaceuticals in an ISO 5 cleanroom environment according to cGMP guidelines and to meet production demands. Tasks include (not limited to) preparing sterilized equipment and components, controlled environment/ equipment cleaning and maintenance, and formulation and dispensing of final product. | 2/19/2021 |
| 9320 | Cyprotex Watertown, MA Scientist/Research Associate BS in Biological or Chemical Discipline Exp: 0-5 Years |
The team is looking for a highly motivated Scientist and/or Research Associate that will be responsible for routine screening of compounds in various assays. Responsibilities: Perform routine in-vitro biological, biochemical, or ADME assays. Responsible for planning, performing and reporting in vitro screening assays for discovery and development stage compounds. Ability to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Assist in data analysis when needed. Laboratory support including ordering, equipment calibration and validation. Working to a high standard and adhering to their Quality System. | 2/19/2021 |
| 9321 | Cyprotex Watertown, MA Research Associate/Assistant BS in Biological or Chemical Discipline Exp: 0-5 Years |
Responsibilities: Perform routine in-vitro biological, biochemical, or assays. Responsible for planning, performing and reporting in vitro screening assays for discovery and development stage compounds. Ability to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Assist in data analysis when needed. Laboratory support including ordering, equipment calibration and validation. Working to a high standard and adhering to our Quality System. Work closely with the Project Managers to ensure the requirements of our clients are met. Assist in running and maintaining robotic systems to support processes. Identify where support is required and manage their own time sufficiently to provide this support. | 2/19/2021 |
| 9322 | Evotec/Cyprotex Waltham, MA Senior Lab Technician - Assay Services MS in Biochemistry, Cell/Molecular Biology, Chemistry, or Related Exp: 1+ Years |
The laboratory technician processes, distributes and ships samples for testing and analysis. May setup and conduct tests, assays, and other protocols under the direction of a laboratory services manager, researcher, or scientist. Follow Standard Operating Procedures (SOPs) and Good Laboratory Practices (GLPs). Ensure all laboratory equipment and work areas are clean, sterile, and in proper working order. Will be responsible for calibration and operation of instruments and data information flow. | 2/19/2021 |
| 9323 | Evotec/Cyprotex Kenilworth, NJ Lab Technician BS in Scientific Discipline Exp: 1-2 Years |
Major Job responsibilities will be manual solid sample weighing and solubilization of the solid samples using an automated liquid handler. The position requires a highly motivated individual, able to work independently, and as part of a team, to ensure successful project support. This role will be expected to have increased understanding of Compound Management workflows, set forth SOPs, etc. Tasks will include but is not limited to performing the day to day laboratory work and direct communication with local and remote lab colleagues in a cross-functional environment. | 2/19/2021 |
| 9324 | Evotec/Cyprotex San Francisco, CA Bioinformatics Associate I MS in Bioinformatics or Related Exp: 0+ Years |
The Microchemistry Proteomics and Lipidomics (MPL) department in Genentech Inc., a client group of Evotec, is looking for a versatile, multi-skilled data scientist to develop novel tools for the analysis of Proteomics, Lipidomics and high-throughput Protein Array datasets. The position will work closely with the computational team as well as bench scientists in the department to understand their technology and deliver the best possible working software prototypes. Demonstrated communication, prioritization, organization skills, as well as the ability to be flexible and responsive in a fast-paced environment are abilities that are highly desired. | 2/19/2021 |
| 9325 | Evotec/Cyprotex Rahway, NJ Research Associate MS in Biological Sciences or Biological Engineering Exp: 0-2 Years |
The candidate will join a cross-functional team responsible driving science forward through engineering optimal expression of recombinant proteins in bacterial expression systems. Candidates will be responsible for the expression of a range of protein targets within the pharmaceutical arena. | 2/19/2021 |
| 9326 | Cytovance Biologics Oklahoma City, OK Manufacturing Sciences & Technology Scientist MS in Life Science Discipline Exp: 0+ Years |
The main responsibility of the Manufacturing Scientist is to support the manufacturing team as a technical advisor and operator. Manufacturing scientists adapt processes demonstrated at the R&D scale to final manufacturing scale. Secondary roles include driving/contributing to continual improvement initiatives and providing input to production scheduling. | 2/19/2021 |
| 9327 | Cytovance Biologics Oklahoma City, OK Quality Assurance Operations Associate BS in Physical or Life Sciences Exp: 0-2 Years |
The QA Operations Associate I is responsible for maintaining quality oversight of operational areas by working closely with Operation’s personnel and performing various checks during manufacturing processes to ensure that current Good Manufacturing Practices (cGMP’s) are followed. The QA Operations Associate I also assess regulatory and quality risks in activities and processes according to GMP and Cytovance Standard Operating Procedures. | 2/19/2021 |
| 9328 | Color Burlingame, CA Clinical Lab Accessioner BS in Life Sciences or Related Exp: 0+ Years |
The Clinical Lab Accessioner will be responsible for assisting in daily clinical operations, primarily involving the performance of a novel clinical test for the testing of COVID-19 in a high complexity CLIA-certified laboratory. Your work will have a direct impact on people’s lives by scaling up the availability of COVID-19 testing and developing much needed public health infrastructure. | 2/12/2021 |
| 9329 | Color Burlingame, CA Clinical Lab Associate BS in Relevant Discipline Exp: 0-2 Years |
The Clinical Lab Associate will be responsible for assisting in routine sample processing for a night shift (10 PM - 6AM, 4 days) in a highly automated, high complexity CLIA-certified laboratory, and you will be working with other laboratory professionals who have joined Color from UCSF, Stanford, Invitae, Counsyl, and other academic and commercial laboratories. Your work will have a direct impact on people’s lives by scaling up the availability of COVID-19 testing and developing much needed public health infrastructure. | 2/12/2021 |
| 9330 | Color Burlingame, CA Automation Engineer BS/MS in Electrical Engineering, Mechanical Engineering, Biotechnology, or Related Exp: 0+ Years |
The ideal candidate approaches problems creatively and with eagerness; you have probably designed a Raspberry Pi controlled device to needlessly automate some aspect of your life, just because you thought it would be fun! We’d love you to join our R&D team, to design new hardware, to build automated products and to create the world's highest throughput and highest quality molecular biology automation stack. | 2/12/2021 |
| 9331 | Conformis Wilmington, MA CAD Engineer I BS in Engineering or Related Exp: 1-2 Years |
The CAD Engineer I will be responsible for designing and reviewing patient-specific implants and surgical instruments using various software packages while ensuring Conformis quality standards. | 2/12/2021 |
| 9332 | Constellation Cambridge, MA Research Associate/Sr. Research Associate, Lead Discovery BS/MS in Biochemistry or Related Exp: 0-5 Years |
Responsibilities: Develop and carry out routine assays to assess compound binding to proteins of interest. Design and perform more detailed experiments to better understand protein function and compound mechanism of action. Analyze data using commercial software tools. Communicate results to project team members, including written reports and oral presentations. Document your work in electronic laboratory notebooks. | 2/12/2021 |
| 9333 | Convelo Cleveland, OH Research Associate/Sr. Research Associate, Lead Discovery BS in Microbiology, Biology, Biochemistry or Related Exp: 0+ Years |
The Research Associate will contribute to the culturing, plating, distribution, maintenance, and banking of cell culture lines, including primary cells and stem cells, as well as immunostaining and imaging these cells within the Research and Development group at a fast-paced start-up company in Cleveland, Ohio to support drug development efforts in the area of remyelination. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in an efficient, highly interactive, goal-oriented team environment, and leading with minimal supervision. As a team member of the R&D group you will work to support cell and tissue culture activities and cellular assays that serve as critical points in a drug screening cascade. | 2/12/2021 |
| 9334 | Cook Medical Bloomington, IN Application Engineer BS in Computer Science, Engineering, or Related Exp: 0+ Years |
The Application Engineer at Cook Medical configures, implements and documents applications that provide the technical solutions to meet specifications and business requirements defined by company objectives to promote effective, efficient, and compliant operations. | 2/12/2021 |
| 9335 | Cook Medical Pittsburgh or Remote, PA Biostatistician MS in Statistics or Applied Mathematics Exp: 1-3 Years |
This position is responsible for providing statistical expertise to clinical development programs. The Biostatistician applies statistical methodology to ensure that the clinical trial designs, programming, and analyses are statistically valid and meet the recognized international standards. | 2/12/2021 |
| 9336 | Cook Medical West Lafayette, IN Scientific Editor BA/BS in Science Related Discipline Exp: 0+ Years |
The Scientific Editor at Cook Research Incorporated will use their skills to support the preparation of medical and scientific documents about established and innovative medical technologies. Scientific editors will provide substantive editorial support for Scientific Communications, Regulatory, and Clinical documents, such as literature reviews, abstracts, posters, presentations, manuscripts, clinical evaluation reports, clinical study reports, and regulatory documents, including IDE and PMA submissions. The successful applicant will demonstrate knowledge and ability in both science and writing/editing. | 2/12/2021 |
| 9337 | Cook Medical Bloomington, IN Sustaining Engineer BS in Biomedical or Mechanical Engineering Exp: 0+ Years |
The Sustaining Engineer at Cook Inc. will lead product and process remediation efforts, in addition to performing sustaining activities for commercially available products. Responsibilities: Interface with Development Engineering, Production Engineering, Product Management, Regulatory, Clinical, Quality Engineering, Quality Assurance, Operations, sourced vendors, and physicians as necessary to progress projects/tasks. Manage multiple project timelines, resources and responsibilities to achieve team, departmental, and company goals. Follow Risk Management procedures and comply with requirements of ISO 14971 as applicable. Follow Design Control procedures and comply with requirements of 21CFR820 Quality System Regulations and ISO 13485 as applicable. | 2/12/2021 |
| 9338 | Cook Medical Winston-Salem, NC Regulatory Reporting Specialist BS in Technical Discipline Exp: 0+ Years |
The Regulatory Reporting Specialist at Cook Winston-Salem is responsible for assessing complaints for Regulatory Reporting, which includes Adverse Event Reporting (MDR, Vigilance, etc.) and associated correspondence to applicable Regulatory bodies. | 2/12/2021 |
| 9339 | Cook Medical Bloomington, IN Change Specialist BS in Relevant Discipline Exp: 0+ Years |
Responsible for facilitating and monitoring the CMMS Document Management and Change Control process from change proposal through release of documentation. Responsible for facilitating training assignments for CMMS documentation and for serving as point of intake for Internal Customer Feedback. | 2/12/2021 |
| 9340 | CooperSurgical Guliford, CT Laboratory Technician BS in Biological Sciences or Related Exp: 0+ Years |
CooperSurgical is seeking to hire a laboratory technician for full time employment in a large-scale culture media manufacturing facility. Candidate will be involved in a wide range of process tasks from maintaining an ISO certified cleanroom to final product. | 2/12/2021 |
| 9341 | CooperSurgical Livingston , NJ PGT-M Laboratory Technician MS in Life Sciences or Related Exp: 1+ Years |
Performs complex molecular-based procedures on clinical samples for the purposes of preimplantation genetic testing (PGT). Analyzes clinical results and provides diagnoses. Performs clinical tasks associated with clinical cases. Assists Supervisor/Manager with documenting and implementing various quality procedures and protocols. | 2/12/2021 |
| 9342 | CooperSurgical Trumbull, CT Product Surveillance Associate II BS in Healthcare Related or Technical Field Exp: 1 Year |
The Product Surveillance Associate II reviews, evaluates, and investigates product complaints relative to the identity, quality, reliability, safety, and effectiveness of CooperSurgical Medical Device and Invitro Fertilization products. The Product Surveillance Associate II is experienced in complaint handling activities and categorizing complaints to comply with current FDA and international reporting regulations. Duties also include supporting the intake of complaints from various sources, initial screening of essential complaint details, Good Faith Effort Follow ups for additional information, Medical Device Reporting (MDR)/Medical Device Vigilance (MDV) determination, investigation assignment, as well as various complaint process activities. In addition to, supporting recall and related field actions in the form of preparing technical documentation and coordinating associated activities. | 2/12/2021 |
| 9343 | Copan Diagnostics Murrietta, CA Laboratory Assistant BS in Relevant Discipline Exp: 1 Year |
The Laboratory Assistant will cover all the microbiological activities and controls related to the raw materials, semi-finished products or finished products, where applicable. The position will also cover all the microbiological activities controls related to environmental controls. | 2/12/2021 |
| 9344 | Copan Diagnostics Chicago, IL Field Service Engineer AS/BS in Industrial, Electrical, or Mechanical Engineering Exp: 0+ Years |
The Field Service Engineer is responsible for administering preventative maintenance (PM) and troubleshooting, calibrating and performing electrical safety tests (EST) on automate microbiology equipment primarily located but not limited to Midwest area of the United States. The ideal candidate is involved in all areas of microbiology equipment technology, including monitoring work order requests, completing repairs, new equipment inspections and installations, PM’s, EST, inventory management, and documenting all service activities. | 2/12/2021 |
| 9345 | CoreRx Pharma Clearwater, FL Quality Assurance Inspector BS/BA in Relevant Discipline Exp: 1-3 Years |
The Quality Assurance Inspector works closely with Manufacturing to ensure quality performance. Responsibilities: Adherence to all company procedures/SOP’s (Standard Operating Procedures). Perform sampling of in-process and raw materials. Release of materials. Participating in the environmental monitoring and water systems. Perform cleaning verifications. Inspections on Labels / Components (Printing and Filling out TM-0210 pages for all inspections or Lab Notebook). | 2/12/2021 |
| 9346 | CoreRx Pharma Clearwater, FL Project Logistics Associate BS/BA in Relevant Discipline Exp: 1-2 Years |
Responsibilities: Work closely with project management and clients to establish required specifications for manufacturing materials from approved vendors and ensure sourced materials are available when required. Ensure materials are sampled by Quality Control and tested per the approved specifications. Work closely with the Quality Unit to ensure results for material testing are completed and submitted for approval in order to release for use in manufacturing. Support projects by locating sources and completing purchase orders as per the established internal processes and procedures. Assist Purchasing with vendor management; factoring in costs, customer service, availability of materials and assessing reliability. | 2/12/2021 |
| 9347 | Covalon Technologies Mississauga, On Associate Scientist (Research and Development) MS in Biology, Chemistry, Chemical Engineering, Biomaterials, or Related Exp: 0+ Years |
As an Associate Scientist for our Mississauga, Ontario head office, you will support a broader team in the design, development, or advancement of currently marketed medical devices to improve patient care. This development can range from prototyping of new products to partnering with third party medical device companies to address unmet or underserved clinical needs. This individual will execute research as outlined by senior team members in a wet chemistry and microbiology laboratory. | 2/12/2021 |
| 9348 | NorthEast Biolab Hamden, CT Intern – Central Lab Services BS Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry, or Exp: some hands-on lab |
NorthEast Biolab is looking for a recent graduate for a lab position in Camden, CT. Duties: Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage; Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials; Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit; Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records; Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices | 02/01/21 |
| 9349 | Catalent Baltimore, MD Associate Scientist I MS in Biology, Biochemistry, Immunology, Bioengineering, or Related Exp: 1+ Years |
This individual performs independently and productively as an Upstream Development Associate Scientist and is actively engaged in process and product development within a dynamic project team. As Associate Scientist I, this person understands and executes most fundamental and some specialized lab techniques focused on cell amplification and protein expressions. With this knowledge, prior to each study they consult with the supervisor and execute a series of experiments independently or with minimal supervision. After the experiment is complete, they assist in data analysis and report generation, actively participate in preparation of the protocol, reports and SOPs. | 1/29/2021 |
| 9350 | Catalent Woodstock , IL Chemist I BS in Chemistry or Scientific Discipline Exp: 0+ Years |
The Chemist I position is responsible for receiving and testing raw materials. Supports laboratory investigations, CoA reviews. The Chemist I plays a crucial role in the Patient First philosophy by analyzing raw material samples and reporting accurate, precise test results in a timely manner to our internal customers. These results ensure our products are made safe, effective and delivered on time to patients. | 1/29/2021 |
| 9351 | Catalent Somerset, NJ Associate Microbiologist BS in Applicable Scientific Discipline Exp: 0-3 Years |
The Associate Microbiologist reports to the Manager, Microbiology and Sample Coordination.Under the supervision of other scientists, the Associate Microbiologist works on problems of limited scope where analysis of data evaluation of identifiable factors. The Associate Microbiologist carries out activities in support of the manufacturing of pharmaceuticals products. These activities include compendial microbial testing of raw materials, in process materials, and finished products within scheduled timelines. | 1/29/2021 |
| 9352 | Catalyst Biosciences San Francisco, CA Contract Clinical Trials Associate MS in Relevant Discipline Exp: 1+ Years |
The incumbent will be involved in all aspects of the overall operation of our clinical studies including project planning, budget, resource management and CRO management. Responsibilities: Daily operations of studies to ensure compliance with applicable GCP/ICH guidelines and other regulatory requirements. Work with cross-functional study teams, including vendors; liaise with other functional areas (preclinical, manufacturing, regulatory affairs) in order to accurately coordinate clinical study activities. Coordinate clinical study timelines with project leaders to meet critical milestones; escalate issues that may jeopardize timelines and deliverables. Track study monitoring visits and co-monitoring visits as needed. Provide updates of study progression. | 2/5/2021 |
| 9353 | Catalyst Biosciences San Francisco, CA Contract Clinical Trials Manager MS in Relevant Discipline & Trial Management Experience Exp: 0+ Years |
The incumbent will manage the overall operation of our clinical studies including project planning, budget, resource management and CRO management. Responsibilities: Manage daily operations of studies to ensure compliance with applicable GCP/ICH guidelines and other regulatory requirements. Manage and lead cross-functional study teams, including vendors; liaise with other functional areas (preclinical, manufacturing, regulatory affairs) in order to accurately coordinate clinical study activities. Coordinate clinical study timelines with project leaders to meet critical milestones; escalate issues that may jeopardize timelines and deliverables. Conduct study monitoring visits and co-monitoring visits as needed. Provide regular updates of study progression to stakeholders. Lead development of study plans and system set-up; participate in preparation and ensure operational excellence of protocol, CRF, CSR and other key study team deliverables. | 2/5/2021 |
| 9354 | Cato SMS Cary, NC Clinical Trial Assistant BS in Life Science or Healthcare Exp: 1-2 Years |
The Clinical Trial Assistant provides technical and administrative support to the clinical project team during all stages of a clinical trial by carrying out administrative in-house-activities. The CTA administers, maintains and coordinates the logistical aspects of clinical trials with a high attention to detail by producing and reviewing documentation, coordinating project details, and maintaining data and filing systems - all with the sense of urgency expected of CATO SMS customers. | 2/5/2021 |
| 9355 | Century Therapeutics Seattle, WA Research Associate/Senior Research Associate - High Throughput Sequencing and Lab Operations BS/MS in Biological, Technical, or Engineering Field Exp: 0-4 Years |
The primary responsibilities of the candidate will be to prepare samples for high throughput sequencing (library preparation) using both standard work flows and robotic platforms; coordinate with CROs to ensure timely data turnaround of sequence data; molecular cloning of plasmids; manage day-to-day lab operations including inventory management/ordering, routine equipment maintenance, and shipping/receiving. They will work closely with both the genomics group and the synthetic biology group to push projects forward. | 2/5/2021 |
| 9356 | Century Therapeutics Philadelphia, PA Research Associate, Cell Engineering MS in Relevant Discipline Exp: 0+ Years |
The Research Associate, Cell Engineering, will support activities to advance our universal iPSC-derived allogeneic cell products for targeting hematological and solid tumors. The Research Associate will be responsible for utilizing existing cell engineering methodologies for gene editing in iPSCs in support of cell therapy efforts. The ideal candidate will work closely with research colleagues, collaborate across functional groups, be self-motivated and able to perform in a fast-paced setting. | 2/5/2021 |
| 9357 | Cerba Research New Hyde Park, NY Associate Scientist - Flow Cytrometry MS in Biology or Related Exp: 1-2 Years |
The Associate Scientist is a key scientific position to support the flow cytometry division in data analysis and data reporting to the clients. The Associate Scientist is critical in identifying data abnormalities and troubleshooting with the help of flow cytometry scientists. The Associate Scientist will have a critical role in reporting quality data to clients. | 2/5/2021 |
| 9358 | Champions Oncology Rockville , MD Sr. Research Associate MS in Relevant Discipline Exp: 1-3 Years |
As a Sr, RA, Flow Cytometry you will performs specialized laboratory tasks in support of preclinical and clinical studies as well as maintaining and collecting data using various systems. Duties and responsibilities include: Performs as the technical lead with new platform development to expand TOS offerings in Flow Cytometry. Technical and general scientific expertise. Flow Cytometry technical competency with immunology and oncology experience. Ensure quality sample analysis, data QC and reporting within defined timelines. Assists Program and Project Leaders in tracking models and animals designated for preclinical research for TOS sponsor studies. Instrument maintenance and troubleshooting. Maintains sample inventories and logs for chain of custody tracking and reporting. Designs panels, validates new antibodies and develops gating strategies up to 8-12 colors. | 2/5/2021 |
| 9359 | Champions Oncology Rockville , MD Research Associate, R&D Flow Cytometry BS in Biology, Immunology, or Related Exp: 1-2 Years |
Associate will perform laboratory tasks in support of flow cytometry assay development for R&D team. Duties and responsibilities: Preparation and handling of primary specimens, including peripheral blood, tumors and other biospecimens. Isolation of PBMC by density gradient separation. Sample preparation (murine or human tissues/cells) for Flow Cytometry and Immunostaining or other assays. Isolation of cell populations with magnetic beads. Assists with ex vivo and in vitro assays with endpoints (e.g. ELISA, cytotoxicity, cytokine profiling). Cell culture experience with cell lines and/or primary cells. Troubleshoot, optimize, and develop methods for unmet experimental needs. Maintain laboratory records and notebook, organize and compile data, and write weekly reports on results. Assist with other tasks/duties/projects as needed. | 2/5/2021 |
| 9360 | Champions Oncology Rockville , MD Laboratory Research Assistant, Histology BS in Veterinary Sciences, Biology, or Related Exp: 0+ Years |
Responsibilities: Assist with gross necropsies (dissection, tissue trimming/collection/preservation, sample collection). Assist with histology samples and submissions. Assist to embed and inventory of human and mouse cancer tissues. Performs slide based histological assays, tests, and procedures and any other such tests in the histology laboratory; including sectioning, staining, macrodissection, and IHC. Assist with recording data using laboratory information management systems. Assist with laboratory and supply inventory. | 2/5/2021 |
| 9361 | Champions Oncology Rockville , MD Research Technician I, Study Services BS/MS in Biology, Pharmacology, or Related Exp: 1+ Years |
As a Research Technician in Study Services, you will support in vivo oncology studies in mice. Additional duties and responsibilities include: Perform in-life technical procedures, handle, restrain, and provide care for all animals. Observe animals for general health and overall well-being. Administer therapeutic agents by various routes. Provide animal welfare assessments, including body weight and tumor volume measurement. Allocate animals to study and non-study groups. Provide preoperative animal care. Euthanize animals as directed in study protocols and directives. Read study protocols and extract pertinent information. Perform study preparation activities including collection tube labeling and room/BSC set-up. Record data using laboratory information management systems. | 2/5/2021 |
| 9362 | Champions Oncology Rockville , MD Research Technician I, Cell Culture (in vivo) BS in Biology, Chemistry, or Life Sciences Exp: 0-2 Years |
As the Research Technician in Cell Culture, your main responsibility is to assist with inventory and culturing of human and mouse cancer cell lines for cell line xenograft studies. Additional duties and responsibilities include: Produce, maintain, and characterize cultured cells, as directed. Work with automated cell counters. Assist with identifying and proposing procedural changes to improve process performance, productivity, and efficiency. Performs related general duties such as inventorying supplies and reagents, general lab housekeeping, and maintaining safety records. Operates and maintains laboratory equipment. Collaborates within department and cross-functionally to meet set objectives. Maintain accurate and detailed records using laboratory information management systems and Microsoft Office suite programs. | 2/5/2021 |
| 9363 | Champions Oncology Rockville , MD Research Technician I, Necropsy BS in Biology, Pharmacology, or Related Exp: 0+ Years |
As a Research Technician in Necropsy you will support the in vivo oncology studies in mice as well as properly euthanize animals in accordance to the company standards and regulations. Additional responsibilities include: Allocate animals to study. Assist with gross necropsies (dissection, tissue trimming/collection/preservation, sample collection). Perform preparation activities, including container and tube labeling and room set-up. Collect, process and maintain blood and tissue samples. Use appropriate anatomic terms and descriptors for lesions. Assist with the tracking and shipment of samples to sponsors and diagnostic laboratories. Conduct and record data in compliance with Standard Operating Procedures (SOPs). Read study protocols and extract pertinent information. Record data using laboratory information management systems. | 2/5/2021 |
| 9364 | Champions Oncology Rockville , MD Research Technician II/III, Cell Culture (in vivo) BS/MS in Biology or Related Exp: 1-4 Years |
Support Ex-vivo / In-vivo oncology studies as a member of the in vivo Cell Culture Team. Duties and responsibilities are: Responsible for inventory and culturing of human and mouse cancer cell lines for cell line xenograft studies. Perform basic and advanced cell culture, including culturing primary cells and characterizing their growth. Produce, maintain, and characterize cultured cells, as directed. Conduct Leukopak PBMC sample processing. Prepare AML and ALL cells for TOS in vitro and in vivo studies. Prepare CAR-T and NK cells for TOS in vitro and in vivo studies. Work with automated cell counters. Efficiently plan and execute cell line scheduling for in vivo studies. Assist in developing scalable processes for upstream and cell culture development. Assist with identifying and proposing procedural changes to improve process performance, productivity, and efficiency. | 2/5/2021 |
| 9365 | ChromaTan Springhouse, PA Associate Scientist I BS in Chemistry, Biochemistry, Chemical Engineering, or Related Exp: 0-2 Years |
This position will support the downstream purification team for development and implementation of a fully integrated end to end continuous bio-production platform fully enabled with PAT. This position will focus on evaluating continuous operation technologies using quality by design techniques, to develop and optimize novel, continuous recovery and purification processes, for recombinant proteins and biological macromolecules. The applicant should have experience in laboratory research, and a desire to continue in a laboratory-focused role. The position will interface with a small team of scientist and engineers focused on continuous chromatography process development and technology transfer to demonstration scale production. | 2/5/2021 |
| 9366 | Cidara Therapeutics San Diego , CA Research Associate, In Vivo BS in Relevant Discipline Exp: 1+ Years |
Animal Technician to conduct in vivo studies in mice at the Cidara vivarium. The successful candidate will be required to work with BSL2 level infectious agents. This position also requires some laboratory work outside the vivarium, at Cidara’s main lab, processing samples for in vitro analysis. This position will directly support the Cidara Cloudbreak antiviral program by providing critical PK/PD and efficacy data to support compound development activities. Position reports to Senior Director, Preclinical Development, and works closely with the Senior Animal Technician. | 2/5/2021 |
| 9367 | Circulomics Baltimore, MD Research Associate BS/MS in Relevant Discipline Exp: 0+ Years |
This is an entry level position in which the applicant's primary responsibility will be to support the development and commercialization of Circulomics technologies including Nanobind, Short Read Eliminator and PicoSep. This work will involve significant exposure to various next-generation sequencing platforms, in particular long-read sequencing technologies from PacBio and Oxford Nanopore. Applicants that show a high degree of independence and aptitude can be expected to gain responsibility quickly and acquire new opportunities. | 2/5/2021 |
| 9368 | Clindatrix Irvine, CA Data Manager BS in Relevant Discipline Exp: 1+ Years |
Responsibilities: Assisting with EDC database testing. Edit check testing. Data review. Query generation and resolution. Responsible for data entry and quality control for paper studies. May assist with writing study documentation and procedures and generating status reports. | 2/5/2021 |
| 9369 | CliniLabs Eatontown, NJ Lab Coordinator BS in Applied Science Exp: 0+ Years |
The Laboratory Coordinator play a crucial role in the execution of clinical research protocols. The overriding purpose of this position is to process and store study biospecimens and assists the operations teams in the growing needs of the studies’ additional lab-related requests. | 2/5/2021 |
| 9370 | CliniLabs Eatontown, NJ Research Assistant/Medical Assistant BS in Relevant Discipline Exp: 0+ Years |
The Research Assistant (RA) is responsible for assisting with document management, protocol related clinical assessments of research subjects, laboratory functions and assisting in tasks related to the work of the Clinical Research Coordinators. | 2/5/2021 |
| 9371 | Clinpace Remote, N/ Contract Analyst BS in Life Sciences Exp: 1-2 Years |
Responsibilities: Assist in establishment and management of contracts submission process and timelines to exceed customer expectations and facilitate an efficient, high quality, and timely submission. Coordinate and prepare budget and contract revisions with Operations Directors, Project Manager, DBD, Project Analyst. Assist Project Managers and DBDs with scope change review with sponsors as needed. Contributes to establishment of payment terms on contracts and change orders with Finance and Legal as needed. Serve as a financial resource to Project Managers or other project team members. Periodic review of project finances, hours, units and milestones to ensure no missed change order opportunities. Partner with the Finance department to assess profit margin and ensure change order proposals capture costs. May need to attend and prepare content for project or company review meetings. Participate in quality or process improvement initiatives. | 2/5/2021 |
| 9372 | Clinpace Morrisville, NC Feasibility Support Analyst BS in Life Science or Healthcare Exp: 1-2 Years |
The Feasibility Support Associate will assist with supporting the Feasibility team through all phases of the study. Duties may include support in coordination, participation and minute taking of meetings, feasibility outreach, site contact, DFS document filing, data entry, tracking, scanning, copying, creating, and maintaining files. | 2/5/2021 |
| 9373 | Clinpace Morrisville, NC Pharmacovigilance Specialist BS in Life Science or Healthcare Exp: 1-2 Years |
The Pharmacovigilance Specialist (PVS) primary responsibility is SAE case management. This includes but is not limited to: initial case disposition, confirmation of case disposition with Medical Monitor (MM)/Safety Physician PV (SP PV), MM, receipt of adverse event data, data entry, source document data extraction, draft narrative development, follow-up management and reporting according to regulatory requirements. All activities will be in accordance with Clinipace and/or client SOPs, ICH Guidelines and local regulatory requirements. | 2/5/2021 |
| 9374 | Clinlogix Lower Gwynedd State, PA Clinical Research Associate BS in Life Sciences or Related Exp: 1-3 Years |
The Clinical Research Associate reports to and works under the direction of the Manager, Global Clinical Monitoring. Responsible to monitor clinical trials, study sites and clinical data while ensuring compliance with protocol and overall clinical objectives and Good Clinical Practice (GCP). Provides administrative and project support to clinical programs with minimum supervision. Interfaces with all project/clinical team members and off-site personnel as needed in support of project and departmental goals and responsibilities. | 2/5/2021 |
| 9375 | Coating Place Verona, WI Associate Formulation Scientist I BS in Chemistry or Related Exp: 0+ Years |
The Associate Formulation Scientist I will support the Associate Manager Formulation Development by assembling, operating, and cleaning processing equipment; preparing coating solutions and other formulas; and performing various analytical testing including but not limited to particle size testing, moisture analysis, and equipment cleanliness verification. The Associate Formulation Scientist I will also work with the Associate Manager Formulation Development to plan and support various pharmaceutical, supplement, food, and industrial projects and will contribute to the development, scale up, and production scale processing as directed by the Associate Manager Formulation Development. | 2/5/2021 |
| 9376 | Coating Place Verona, WI QC Analytical Chemist BS in Chemistry or Related Exp: 0+ Years |
The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. | 2/5/2021 |
| 9377 | Coating Place Verona, WI QC Associate Scientist BS in Chemistry or Related Exp: 0+ Years |
The primary purpose of the QC Associate Scientist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, research procedures, and miscellaneous protocols. The Associate Scientist is expected to understand internal procedures and reliably conduct analyses with limited supervision. | 2/5/2021 |
| 9378 | Coating Place Verona, WI QC Analytical Chemist I BS in Chemistry or Related Exp: 0+ Years |
The primary purpose of the QC Analytical Chemist 1 is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, research procedures, and miscellaneous protocols. The QC Analytical Chemist 1is expected to understand internal procedures and reliably conduct analyses with minimal supervision after training. | 2/5/2021 |
| 9379 | Coating Place Verona, WI QC Analytical Chemist II BS in Chemistry or Related Exp: 1+ Years |
The primary purpose of the QC Analytical Chemist 2 is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, research procedures, and miscellaneous protocols. The QC Analytical Chemist 2 is expected to understand internal procedures and reliably conduct analyses with minimal supervision. | 2/5/2021 |
| 9380 | Codexis Redwood City, CA Research Assistant I/II, Upstream Bioprocess Development BS in Chemical Engineering, Biochemistry, Biological Science, or Related Exp: 0-2 Years |
As part of this dynamic team you will work with upstream process development scientists to generate critical data of fermentation and primary recovery scale down experiments for performance enzymes. Initially you will perform analytical assays to characterize upstream processes and progress to participating in process development experiments to improve performance and robustness of manufacturing processes. | 2/5/2021 |
| 9381 | Codexis Redwood City, CA Research Assistant/Associate, Biotherapeutics Lead Discovery BS/MS in Biochemistry, Structural Biology, Bioengineering, or Related Exp: 0-6 Years |
Responsibilities: In collaboration with cross-functional project team members, perform high-throughput (HTP) screening campaigns to support directed evolution of next-generation biotherapeutics. Express recombinant protein variants in E. coli or mammalian cells for in vitro profiling. Execute and troubleshoot assay protocols for protein characterization (e.g., biochemical, enzyme activity, and cell-based assays). Adapt assays for HTP screening. Actively participate in project teams, present research updates, and collaborate with cross-functional team member. Maintain a safe and efficient workplace, follow safe lab practices, keep diligent records, and write reports and SOPs as needed. | 2/5/2021 |
| 9382 | Codexis Redwood City, CA Research Assistant/Associate, High Throughput Screening & Selection BS in Relevant Discipline Exp: 1-3 Years |
As part of this team you would support the development and discovery of novel enzymes by contributing to the efforts of the high throughput protein expression laboratory. Responsibilities: Fulfilling requests for high throughput protein expression using lab automation including liquid handlers and automated colony pickers in a team setting. Assist in the development and optimization of high throughput protein expression protocols for bacterial and fungal organisms. Track and update request data in an automated LIMS system. Work collaboratively with internal clients to troubleshoot issues and update status of internal requests. | 2/5/2021 |
| 9383 | Codiak BioSciences Cambridge , MA Technical Support Engineer BS in Electrical, Mechanical, Industrial, or Computer Engineering Exp: 1-4 Years |
As a Technical Support Engineer, you will report to the Head of IT. As a member of the IT team, you will be responsible for ensuring timely and accurate resolution of technical issues for Codiak’s employees. You will also contribute to the initiatives to improve efficiency and service levels. | 2/5/2021 |
| 9384 | CogMedix West Boylston, MA Electrical Engineer I BS in Electrical Engineering Exp: 0-5 Years |
As a member of the engineering services team, the Electrical Engineer I will solve complex problems and participate in the specification, design, prototyping and testing of a diverse range of tooling, fixtures, design for manufacturability projects, and other customer product design needs. Under the direction of the Electrical Engineering Manager, the engineer in this role will be performing design tasks of a complex technical nature requiring investigation of new technologies, and applying engineering design principles and practices. | 2/5/2021 |
| 9385 | Cognate Bioservices Memphis, TN QC Analyst I - Bioassay BS in Biological Sciences or Related Exp: 0-3 Years |
Responsibilities: Adheres to Standard Operating Procedures (SOPs) and good documentation practices to ensure data integrity and traceability. Perform cell based immunological in vitro methods (e.g., cytotoxicity, HLA-restriction, cell proliferation, etc). Perform release testing utilizing a variety of techniques ranging from compendia assays like pH and osmolality to more complex assays like, but not limited to, proliferation and cytotoxicity. Be able to quickly learn various methods and participate in the troubleshooting of assays. Enters observations and results into the appropriate trending databases for periodic analysis and trending. | 2/5/2021 |
| 9386 | Cognate Bioservices Memphis, TN Quality Ops Specialist I BS in Life Sciences or Related Exp: 0-1 Years |
Responsibilities: Review manufacturing Batch Production Records (BPRs) and associated supporting documentation including logbooks, Quality Control (QC) testing reports, environmental monitoring reports, etc. Perform line clearance and provide general manufacturing support. Supports product shipment and receipt of returns. Support raw material review and disposition. Review Building Management Systems reports. Participate in departmental and cross-functional continuous improvement efforts. Consistently set a high standard for quality of work. Promote a safety mindset through daily actions and communication with team members. | 2/5/2021 |
| 9387 | Coloplast Minneapolis, MN Associate Packaging Engineer BS in Packaging Engineering or Related Exp: 1+ Years |
You will be assisting in performing original packaging design and testing, over a broad range of technologies to provide new or improved products to the medical device market, in the arena of Interventional Urology. In this role, you will act as a technical support person for interdepartmental development teams, in order to fulfill business goals of Coloplast for new and existing product packaging and labeling. | 2/5/2021 |
| 9388 | Coloplast Minneapolis, MN Regulatory Affairs Specialist BS in Relevant Discipline Exp: 0-2+ Years |
You will be responsible for design control compliance for assigned products and will support development and execution of regulatory strategies per time lines to assure clearance / approval in the assigned geographies. In this role, you will also prepare, monitor and communicate status of regulatory submissions and perform duties related to regulatory affairs post-market surveillance, change analysis, claims review and vigilance reporting. | 2/5/2021 |
| 9389 | Cambrex Whippany, NJ Microbiologist BS in Biology or Microbiology Exp: 1-2 Years |
The Microbiologist will maintain product quality by conducting microbiology associated tests and monitoring on the manufacturing and packaging environments and systems while adhering to cGMP guidelines. Responsibilities: Perform Environmental Monitoring by sampling: Total Particulates, Viable Air, Surfaces. Support aseptic processing in a clean room environment including the ability to aseptically gown in to an area and monitor the environment. Sample the water systems and perform the microbiology testing on water samples: Bioburden and Bacterial Endotoxin testing. Perform quality control microbiology testing on incoming organisms, media, reagents, etc. Clean and maintain laboratory equipment. | 1/29/2021 |
| 9390 | Cambrex Charles City, IA Microbiologist BS in Biology or Chemistry Exp: 0+ Years |
The Microbiologist will be responsible for daily testing of microbiology samples, water testing, and for other duties as assigned. Responsibilities: Provide laboratory testing support for the Cambrex Charles City Quality Control group. Perform chemical testing with supervision using analytical instrumentation including TOC, conductivity meter, and Endotoxin reader. Perform chemical testing with supervision using standard compendial test methods such as identification, microbial analysis, etc. Write and execute microbial methods and validation protocols. Adhering to SOPs and regulatory systems as they relate to laboratory testing operations; e.g. cGMP compliance and training. | 1/29/2021 |
| 9391 | Cambrex Charles City, IA Process Engineer BS in Chemical Engineering Exp: 1-3 Years |
The Process Engineer will be responsible for implementation of projects for the manufacture of APIs and bulk intermediates and other products from development through piloting and/or commercial production. Responsibilities: Writing batch records, cleaning records, SOPs, campaign reports, supplements, and investigation/deviation reports as needed to support production operations. Monitoring KPIs and using process data to identify and execute improvements to new and existing products to achieve improved yields, quality or customer expectations. Working with process improvement to identify and execute Kaizen events. Providing training and process support to production areas including training on new processes and on-site oversight of key processing steps. | 1/29/2021 |
| 9392 | Canfield Parsippany, NJ Clinical Project Associate AS/BS in Relevant Discipline Exp: 0+ Years |
An ideal candidate for our Clinical Project Associate position is an individual who has the ability to prioritize and multitask, is experienced in Microsoft Operating Systems, and possesses strong organizational and communication skills. Responsibilities: Support the project team on designated projects ensuring that customer service, quality, and timelines are met. Perform quality control checks to ensure the integrity of data. Aid in the preparation of supply shipments to study sites. Setup, maintain, and update databases and assist with data query resolution. Ensure proper filing of all study documents and under direct supervision communicate with study sites by fielding, answering, and directing questions to obtain appropriate answers. | 1/29/2021 |
| 9393 | Caprion Fremont, CA Research Assistant BS/MS in Immunology or Cell/Molecular Biology Exp: 1-3 Years |
Performs complex immune monitoring assays for clinical samples. Participates in writing of procedures (SOP/CSP). Trains other laboratory personnel on technical procedures/methods. Records associated documentation relevant to the tasks at hand as per appropriate SOP and applicable GLP regulations and GCLP guidelines. | 1/29/2021 |
| 9394 | Cardinal Health Remote, N/ Scientist I, Chemistry, Manufacturing & Controls CMC BS in Relevant Discipline Exp: 0+ Years |
Responsibilities: Assist in the assembly of regulatory information for submission. Adheres to the client's defined submission preparation timelines. Searches document and change management databases for historical data/information that need to be captured in the updated regulatory submission. Using the client's templates for dossier sections, author CMC sections for routine submissions (e.g., clinical trial amendments, Type I variations, IND/NDA/BLA annual reports, CMC renewals), including adding technical data and descriptive text. | 1/29/2021 |
| 9395 | Cardinal Health Mansfield, MA R&D Engineer BS in Engineering Exp: 0-2 Years |
The engineer will support the Design and Development Services team. The DDS team supports legacy products and new product development designs through ensuring adherence to design controls, industry standards and internal SOPs. The DDS team supports MDD/MDR compliance from an R&D perspective for products sold in CE-marked countries. Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. | 1/29/2021 |
| 9396 | Cardinal Health Roseville, MN Nuclear Pharmacy Technician BS in Relevant Discipline Exp: 0+ Years |
Nuclear Pharmacy is responsible for providing radiopharmaceuticals and other drugs to medical care providers under highly regulated State and Federal guidelines; may also consult with or advise physicians and nuclear medicine technologists on the safe and efficacious use of radioactive drugs for diagnosis and therapy | 1/29/2021 |
| 9397 | Cardinal Health Fort Lauderdale, FL Technician I, Chemical/Pharmaceutical Operations BS in Relevant Discipline Exp: 0-6 Months |
Operates automatic and manual manufacturing and chemical process equipment of varying complexity in various production processes in accordance with operating procedures. Performs a variety of tasks related to the processing of ingredients and/or pharmaceutical products. Handles raw materials and intermediate or finished products. Mixes compound ingredients for liquid products, suspensions, ointments, mixes, or blends for tablet granulations and capsule powders. May perform general maintenance as required on pumps, homogenizers, filter presses, tablet compression machines, etc. Performs standard operating procedures to meet current good manufacturing practices (GMP). Maintains records as required. May monitor and verify quality in accordance with statistical process or other control procedures. | 1/29/2021 |
| 9398 | CardioFocus Remote, N/ Field Clinical Specialist BS in Engineering Exp: 1-2 Years |
Working with the US Sales & Marketing team in a collaborative and cross-functional setting, the Field Clinical Specialist will participate with the US Sales & Marketing team in the field support and education using the Company’s unique Endoscopic Ablation System in the treatment of patients with atrial fibrillation (AF). | 1/29/2021 |
| 9399 | CareDx Brisbane, CA Process Development Engineer MS in Life Sciences, Biotech, Molecular Diagnostic or Medical Device Industry Exp: 1+ Years |
CareDx is seeking an independent and highly motivated Process Development Engineer to monitor and improve a diverse collection of manufacturing processes. These include the processing of patient samples through the CLIA-certified laboratory, as well as Formulation, Reagent QC, and Filling processes in Reagent Manufacturing. The successful candidate will understand the criticality of each step of the process and closely monitor the key performance indicators that can improve the critical outgoing metrics. They will work closely with R&D, the Clinical Lab, Process Development and Manufacturing to ensure new processes are transferred smoothly. | 1/29/2021 |
| 9400 | CareDx Brisbane, CA Clinical Lab Scientist BS in Biological Science, CA CLS License Exp: 1-6 Years |
The Clinical Laboratory Scientist (CLS) performs testing in the CLIA-certified laboratory, participates in quality control, quality assurance and troubleshooting activities. A CLS performs duties under general direction, carrying out work assignments in accordance with policies and objectives established by the Clinical Laboratory Manager (CLM)or designee. A CLS is expected to plan and organize his or her own work, determining work methods and assisting in the determination of priorities and deadlines. Completed work is reviewed by the CLM or designee to verify the achievement of expected results. | 1/29/2021 |
| 9401 | CareDx Brisbane, CA Clinical Laboratory Assistant BS/BA in Biological Science Exp: 1-3 Years |
The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed. | 1/29/2021 |
| 9402 | Johnson & Johnson Seattle, WA Surgical Data Analyst, Products and Programs BS in Scientific Discipline Exp: 0+ Years |
Responsibilities: Define surgical steps and tasks to break down the surgical videos for technical assessments for surgeons. Ensure security of PHI from the surgical videos and surgeon’s information with acute attention to detail when handling sensitive data. Build innovative surgical content to help educate surgeons across all surgical methods and procedures. Accountable for the delivery of critical business projects, continuously ensuring alignment and prioritization of C-SATS objectives with business needs. S/he must establish and maintain a positive, proactive, high-energy, collaborative and engaging work environment. Collaborate with R&D and Machine Learning organization to help implement integrative technology to process surgical procedures efficiently. | 1/29/2021 |
| 9403 | Johnson & Johnson Lititz, PA QC Scientist I BS in Chemistry Exp: 1+ Years |
Responsibilities: Routinely tests raw materials and finished products for conformity to specification using standard operating procedures, including testing using wet chemistry techniques. Record results of testing in laboratory workbooks, directly on report forms or into the laboratory computer system, making standard calculations as required to obtain final results utilizing good documentation practices. Assure that instruments used in analytical methods are calibrated and performing accurately. Confer with team leader on issues and works in conjunction to develop or improve methodology. Communicate issues, or potential issues, as well as proposes solutions to the Team Leader in a timely manner. Update Standard Operating Procedures and Job Aids as needed. | 1/29/2021 |
| 9404 | Johnson & Johnson Malvern, PA Associate Scientist I, Drug Product Development MS in Chemical, Mechanical, Electrical, or Biomedical Engineering Exp: 1-3 Years |
The Associate Scientist I will be a member of a formulation/process development team within the Drug Product Development (DPD) – BioTherapeutics (BioTD) department. The Associate Scientist I will be involved with DPD activities related to implementation of fill/finish processing at the development stage and manufacturing scale pertaining to monoclonal antibodies, cell-based therapies and virus like modalities to name a few. | 1/29/2021 |
| 9405 | Johnson & Johnson Raritan/Spring House, NJ Clinical Research Associate - College Hire BS/MS in Health Sciences or Related Exp: 0+ Years |
The College Hire, Global Clinical Operations (GCO) will gain knowledge of and support activities of the Local Trial Manager and Site Manager positions under the direct supervision of a Local Trial Manager/Site Manager II, Program Manager, and/or Functional Manager responsibilities within assigned Therapeutic Area(s). LTM: to provide operational oversight of protocols from start-up through database lock and closeout activities as described in GCO procedural documents. SM: to serve as a primary contact point between the sponsor and the investigational site. | 1/29/2021 |
| 9406 | Johnson & Johnson Spring House, PA Associate Scientist, Lead Evaluation and Cellular Pharmacology MS in Biochemistry, Cell Biology, or Related Exp: 1+ Years |
Responsibilities: Learn and apply state-of-the-art drug discovery approaches as part of a dynamic, multidisciplinary cellular assays team. Develop and implement innovative cell-based assays to identify and evaluate lead compounds using high-content imaging, gene expression profiling, 3D cell culture and/or co-culture methods. Work closely with computational biology colleagues to analyze high-content data and identify promising leads compounds. Attend and present data at program team meetings and in-house seminars. Publish research in high-quality journals, as appropriate. | 1/29/2021 |
| 9407 | Johnson & Johnson San Diego/La Jolla, CA Associate Scientist, Analytical Chemistry - Discovery Chemistry MS in Analytical, Synthetic, Organic, or Medicinal Chemistry Exp: 0+ Years |
In this laboratory-based position, the successful candidate will provide analytical support to medicinal chemists. This includes the confirmation and identification of compound structures using NMR and LCMS, and open access analytical instrument maintenance. She/he will maintain close interactions with scientists from Discovery Chemistry and Discovery Process Research to expedite the compound Design-Make-Test iterations. Strong communication skills and the ability to thrive in a team and results oriented environment are key attributes. This individual must also have strong interpersonal skills necessary to influence in a collaborative multidisciplinary environment. | 1/29/2021 |
| 9408 | Johnson & Johnson Boston, MA Electrical Engineer, Orthopedic Robotics BS/MS in Electrical Engineering or Related Exp: 1+ Years |
This role represents an exciting opportunity for a candidate who wants to work on building groundbreaking surgical capabilities for Orthopaedic Robotics. The Electrical Engineer will work on a new Surgical Robot for Orthopaedic Surgery from the development phase through commercial release, as well as future robots. | 1/29/2021 |
| 9409 | Phillips Wichita, KS Field Service Engineer BS in Biomedical, Industrial, Mechanical, or Electrical Engineering Exp: 0+ Years |
This position is an entry-level position for an employee with limited experience. The focus is learning how to provide an outstanding customer experience, become a viable team member and quickly get up to speed with technical expertise. The FSE will learn to work independently as well as in a team environment while under direct supervision. The Field Service Engineer position supports the Precision Diagnosis & Image Guided Therapy business within an assigned geographical area. This position will be responsible for customer relationship management through the effective use of technical knowledge to install, troubleshoot, service, and maintain equipment at customer sites; generate service revenue; adherence to state and federal regulatory requirements. | 1/29/2021 |
| 9410 | Phillips Carbondale, IL Field Service Engineer BS in Mechanical, Electrical, or Biomedical Engineering Exp: 0+ Years |
In this role, you have the opportunity to work on some of the most complex challenges in healthcare by utilizing your skills in data structures, systems knowledge, algorithms, and object oriented programming. As a field service engineer at Philips, you are the bridge between abstract concepts and the technology products used daily to touch the lives millions of other people around the world. | 1/29/2021 |
| 9411 | Phillips Chicago, IL Field Service Engineer BS in Biomedical, Industrial, Mechanical, or Electrical Engineering Exp: 0+ Years |
Responsibilities: Operate under the required knowledge of State and Federal regulatory requirements. Adheres to established training, quality, and safety requirements. Manages company assets effectively in accordance with established Philips processes and guidelines including labor time, parts ordering and returns, tools and test equipment calibration, purchase orders, equipment, company vehicles, business expenditures, etc. Performs all administrative duties within established Philips and regulatory timeframes including timesheets, service work orders, expense reports, Field Change Orders, preventative maintenance, installation documents, site and service documentation, and other related paperwork. | 1/29/2021 |
| 9412 | Phillips San Diego , CA IVUS R&D Engineer BS in Biomedical, Mechanical, Plastics, or Electrical Engineering, or Materials Science Exp: 1+ Years |
Provides technical expertise to the design and development of new invasive and noninvasive medical device product(s). Designs and implements new methodologies, materials, machines, processes, or products. Develops new concepts from initial design to market release. Conducts feasibility and verification studies of the design and design related processes/test methods to demonstrate intended function. Maintains detailed documentation throughout all phases of research and development. Coordinates activities with outside suppliers and consultants to ensure the delivery of supplies or services needed to meet scheduled timelines. | 1/29/2021 |
| 9413 | Phillips Monroeville, PA Mechanical Engineer - Oxygenation & Ventilation BS/MS in Mechanical, Biomedical, Plastics, or Related Engineering Exp: 0+ Years |
In this role, you have the opportunity to participate in the design, implementation, test, and documentation efforts necessary to support the development of mechanical components for use in Oxygenation and Ventilation medical devices. This role is for Research and pre-development. The candidate will work on tasks and assign tasks necessary to meet project goals for products being developed for Sleep and Respiratory Care. | 1/29/2021 |
| 9414 | Phillips San Diego , CA Digital Electrical Engineer BS/MS in Electrical Engineering Exp: 0+ Years |
As an Electrical Engineer, you will be responsible contributing to the design and development of intravascular imaging and functional measurement devices. You will utilize your knowledge and expertise in circuit design and testing to create market-leading products. This position within IGT-D R&D collaborates closely with other R&D functions (mechanical, systems, etc.), Marketing, Clinical Affairs, Procurement, and Quality Regulatory. | 1/29/2021 |
| 9415 | Phillips Monroeville, PA Cleaning & Disinfection Test Engineer BS in Engineering Discipline or Equivalent Exp: 1+ Years |
The Cleaning and Disinfection Test Engineer focus is to generate C&D test protocols, conduct testing internally and externally and document results. Responsibilities: Assess failures and coordinate corrective actions with project teams. Review product requirements with development teams to ensure that they are complete and testable. Coordinate C&D Formal Technical Reviews with cross functional group to plan and execute strategies. Interact with Technical Writers to ensure product labeling complies with executed test procedures. | 1/29/2021 |
| 9416 | Caris Life Sciences Phoenix, AZ Research & Regulatory Coordinatior BS in Scientific Discipline Exp: 1-2 Years |
The Research and Regulatory Affairs Coordinator is responsible for providing regulatory administrative support to the Clinical Research Operations group for Caris sponsored research studies. Specific responsibilities: Maintain intake of assigned research project IRB approvals and expiration documents. Monitor local site IRB and WIRB activities, including additional site submissions, amendments/changes in research submissions, create/facilitate submission of annual continuing review reports, monitor and notify of document expiration dates, and process fees through accounts payable. Liaison between Caris and physician investigator(s), research institute(s), contract research organization(s), regulatory agencies and other designated stakeholders. | 1/29/2021 |
| 9417 | Caris Life Sciences Phoenix, AZ Research Associate I-III BS/MS in a Biological Science related to Molecular Biology Exp: 0+ Years |
Research Associates are responsible for conducting scientific research leading to the discovery and development of high value, proprietary molecular diagnostic products and related technologies. A strong understanding of molecular biology, molecular genetics, aptamer development and validations is highly preferred. | 1/29/2021 |
| 9418 | Caris Life Sciences Phoenix, AZ Laboratory Operations Specialist - Pathology BS in Scientific Discipline Exp: 0+ Years |
The Laboratory Operations Specialist is responsible for supporting all CMI laboratory departments with all clerical and ancillary duties in keeping all equipment ready to run for patient output. While maintaining job functions, the Laboratory Operations Specialist is to progress in their learning of the regulations (CLIA, CAP and NYS) which the laboratory functions by. Laboratory Operations Specialists support Specimen Processing Clerks, Histology Technicians, Histology Technologists, Pathology Assistants, Pathologists and Molecular Technicians. This position works under the direction of the Supervisor and follows standard laboratory procedures and policies. | 1/29/2021 |
| 9419 | Caris Life Sciences Phoenix, AZ Quality Assurance Technologist - Molecular BS/MS in Scientific Discipline Exp: 0+ Years |
A Quality Assurance Technologist is responsible for a multitude of different tasks within the clinical molecular laboratory including the quality control testing of all molecular reagents prior to use on clinical samples, assisting the product development team with the validation of new assays and training current employees on new assays as well as new employees on established assays This position is required to be well versed in various molecular techniques that include, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, RFLP, DNA methylation analysis, Next Generation sequencing and automated liquid handlers. Quality Assurance Technologists are expected to contribute technically and intellectually to enhance efficiency within the lab while ensuring that the quality of reagents and training program is maintained to the highest standard. This position works under the direction of the Director and follows standard laboratory procedures and policies. | 1/29/2021 |
| 9420 | Caris Life Sciences Phoenix, AZ Jr Bioinformatics Scientist MS in Bioinformatics, Biostatistics, Biomedical Engineering, or Related Exp: 0+ Years |
Caris Life Sciences is looking for a sharp, driven and goal oriented Jr Bioinformatics Scientist to support their bioinformatics and statistical analysis leadership as well as novel biomarker discovery derived from Caris’ proprietary ADAPT Biotargeting SystemTM. These critical roles will work closely with the Bioinformatics & R&D teams to assist in designing experiments, analyzing complex clinical and translational data sets. They are looking for team oriented, hands on professionals with a passion for personalized medicine and innovation in statistical and mathematical analyses. | 1/29/2021 |
| 9421 | Caris Life Sciences Phoenix, AZ Bioinformatics Scientist MS in Bioinformatics, Biostatistics, Biomedical Engineering, or Related Exp: 0-8 Years |
Bioinformatics scientists provide bioinformatics and statistical analysis support for biomarker discovery, IVD product development and CMI tumor molecular profiling service. Responsibilities: Develop and maintain statistical analytical tools and bioinformatics pipelines. Conduct analysis and develop innovative algorithms on biomarker discovery and clinical diagnostics data. Consult on experiment design and data interpretation for laboratory research. Provide analytical support for quality assessment of laboratory service and production data. Contribute to design and development of informatics infrastructure. Adhere to coding and documentation standards and manage deliverables for area of responsibility. | 1/29/2021 |
| 9422 | Caris Life Sciences Phoenix, AZ QC Specialist - Reagent QC BS in Scientific Discipline Exp: 0+ Years |
The Quality Control Specialist is responsible for maintaining regulatory compliance to all applicable regulatory requirements. Responsibilities: Maintain regulatory compliance to all applicable regulatory requirements (CLIA, NYS, CAP, FDA, ISO, etc.). Ensure that QC Testing of incoming reagents and materials is performed and documented according to applicable procedures. Release reagents and materials for use within the appropriate systems. Communicate material issues to the cross-functional team, as necessary. Capture Quality Control metrics for trend analysis. Identify opportunities for improvement. | 1/29/2021 |
| 9423 | Carmine Therapeutics Cambridge, MA Senior Research Associate, Biology BS/MS in Biology, Immunology, Biochemistry or Related Exp: 0+ Years |
Responsibilities: Support preparation of engineered red blood cell extracellular vesicles (RBCEVs). Perform cell culture experiments to characterize RBCEVs. Support animal studies from dosing to downstream sample processing and analysis. Perform immunohistochemistry and in-situ hybridization experiments. Analyze and interpret experimental data. Maintain accurate and detailed documentation including electronic lab notebook. General laboratory assistance including organizing lab supplies, preparation of reagents, and lab equipment maintenance. Present research findings in the internal meetings. | 1/29/2021 |
| 9424 | Carmine Therapeutics Cambridge, MA Senior Research Associate, Molecular Biology BS/MS in Biology, Biochemistry or Related Exp: 0+ Years |
Responsibilities: Develop molecular assays to support payload optimization. Execute molecular biology experiments to generate payload for RBCEV delivery. Support preparation of engineered red blood cell extracellular vesicles (RBCEVs). Perform cell culture experiments to characterize RBCEVs. Analyze and interpret experimental data. Maintain accurate and detailed documentation including electronic lab notebook. Manage an organized laboratory environment ensure smooth day-to-day operations. Prepare and present research findings internally. | 1/29/2021 |
| 9425 | Catalent Baltimore, MD Laboratory Assistant AS/BS in Life Sciences Discipline Exp: 0-1 Years |
The successful candidate will perform various tasks to support AD analysts, including Reagent Preparation, Inventory Maintenance/Ordering and maintenance of GMP notebooks/records. The Laboratory Assistant is expected to assist various groups within Analytical Development and help with maintenance of GMP compliance in multiple laboratories within AD. | 1/29/2021 |
| 9426 | Catalent Baltimore, MD Associate Scientist III MS in Chemical Engineering, Chemitry, Biochemistry, or Life Sciences Field Exp: 1-3 Years |
The Associate Scientist III - Downstream Process Development responsible for providing leadership and support to the Catalent Cell and Gene Therapy sites. The Department has the responsibility for developing upstream and downstream manufacturing processes utilizing novel technologies to produce state-of-the-art therapies for people when they are most in need. As a Catalent Cell and Gene Therapy employee, you will actively contribute to the delivery of Catalent services and products to customers and their patients. | 1/29/2021 |
| 9427 | Catalent Bloomington, IN Associate Quality Engineer - Deviation Writer BS in STEM Discipline Exp: 0-2 Years |
This role will be responsible for working with our Quality Engineering team to ensure each deviation is thoroughly investigated and quality impact assessed. Specific Responsibilities: Supports the manufacturing of pharmaceutical products. Conduct direct contact with clients and internal customers across the site. Ensure that documentation is accurate and effectively assessing and mitigating risk associated with manufacturing activities. Suggest Corrective and Preventative Actions (CAPAs), take ownership for their deviations and drive to meet deadlines. Perform Root Cause Analysis and Investigations in Trackwise. | 1/29/2021 |
| 9428 | Catalent Madison , WI Associate, QA Operations BS in Biology, Biotechnology, Engineering, or Related Exp: 0+ Years |
The QA Operations Associate assures that all operations at Catalent meet or exceed cGMP regulations and client customer requirements. The QA Operations Associate assures the quality of Cell Banks and Bulk Drug Substance produced and supports release of BDS for further clinical manufacturing of drug product. This position also ensures quality of manufacturing and laboratory data and reports. This is accomplished by direct collaboration and oversight of Manufacturing Operations and Quality Control and the review/audit of data and reports as specified by Standard Operating Procedures. | 1/29/2021 |
| 9429 | Biotechne Minneapolis, MN Process Automation Engineer BS in Engineering or Technical Science Exp: 1-3 Years |
You will work within a highly dynamic group serving as a resource for implementation, expansion and enhancement of automation solutions used in Manufacturing and Fill/Finish Operations. You will play a key role in expanding the use of Automation to increase manufacturing efficiency. | 1/22/2021 |
| 9430 | Biotechne Minneapolis, MN Advanced Research Associate MS in Relevant Discipline Exp: 0-2 Years |
This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product.ﾠ The position requires maintenance of cell lines and isolation of primary cells for use in the assays.ﾠ Good Manufacturing Practice (GMP) documentation and workflow is required in this position.ﾠ Participate in troubleshooting as needed.ﾠ | 1/22/2021 |
| 9431 | Biotechne Minneapolis, MN Research Associate, Fermentation BS in Biotechnology or Related Exp: 0-2+ Years |
This position is responsible for the production of Animal free cell paste by means of various types of bioreactor/fermentation systems. Work in a highly regulated, GMP, cleanroom environment. Generate cell banks, performs small- and large-scale fermentation for protein production.ﾠ Analyze productivity as required, based on SDS PAGE Gels, bioassay results and Western blots.ﾠ Provide documentation of performed tasks and assists in establishing written procedures to accurately document production of protein. Assist with the purification and final bottling of products as time allows. | 1/22/2021 |
| 9432 | Biotechne Newark, CA Senior Research Associate MS in Molecular Biology, Biochemistry, Cell Biology, or Related Exp: 0-2 Years |
You will be a key member of the ACD Service Department, performing RNAscope assay services for industrial, pharmaceutical, and academic clients. You will also have the opportunity to work closely with scientists and investigators from a broad customer base. You must be willing to learn new techniques quickly and be able to adapt to shifting priorities in a fast-paced and growing environment. | 1/22/2021 |
| 9433 | Biotechne Devens, MA Quality Technician - Statistics BS in Science or Quality Field Exp: 0+ Years |
Quality Technician- Statistics has the ability to work independently, analyze results and determine whether product specifications are met. Technician participates in instrument lab maintenance activities, by consistently monitoring laboratory and process inventories and conducting log book and device history record review. In addition to Quality Technician responsibilities, Quality Technician- Statistics is the primary person responsible for the efficient operation of the Statistical Program database for all OEM, RNA or Hospital customers. | 1/22/2021 |
| 9434 | Biotechne Woburn, MA Product Engineer BS/MS in Chemical Engineering, Polymer Science, Materials Science, or Related Exp: 1-3 Years |
As part of an interdisciplinary team, this position will support development and troubleshooting of novel polymeric reagents for cell and gene therapy research and clinical use. The role will focus on formulating new hydrogel microspheres to deliver scalable, repeatable and functional product for a variety of internal and external customer projects.ﾠ Additionally, the Product Engineer will contribute to developing new chemical, imaging and cell based analytical tools with opportunity to collaborate with technical groups across Bio-Techne. | 1/22/2021 |
| 9435 | Biotechne Newark, CA Research Associate, R&D BS in Molecular Biology, Biochemistry, Cell Biology, or Related Exp: 1+ Years |
Responsibilities: Execute RNAscope/BaseScope/miRNAscope-based assays to support new product development and assay optimization, including but not limited to RNAScope/BaseScope/miRNAscope assay testing, R&D collaboration projects and RUO raw material improvement projects. Support manufacturing QC for commercial product testing, release and troubleshooting when needed. Facilitate SOP/SPK/SPJ drafting/assay QC procedure transfer from R&D to QC team. Participate in R&D/QC communication and hands-on training. Responsible for experimental design, assay running, data collection and interpretation. Maintain sample inventory and logs for slides. | 1/22/2021 |
| 9436 | BioTek Winooski, VT Product Development Engineer MS in Mechanical, Electrical, Biomedical or Chemical Engineering Exp: 0+ Years |
In this position, you will act as a Product Development Engineer for new product development and upgrades to existing products. You will participate in all aspects of the product development process as well as support manufacturing and service in resolving product problems that arise following relevant FDA regulatory guidelines and ISO procedures. | 1/22/2021 |
| 9437 | Bluebird Bio Cambridge, MA Associate Scientist I BS/MS in Molecular Biology, Biochemistry or Related Biological Science Exp: 0-2 Years |
The focus of this position is to provide support for assay development and testing to characterize lentiviral vector, drug product, and genome editing reagents. Responsibilities: Design and perform experiments to support the development of analytical assays for molecular characterization of lentiviral vectors, mRNA, and cell therapy products. Learn and implement new laboratory techniques and equipment. Perform general laboratory tasks including ordering, reagent preparation, and equipment maintenance. Generate, manage, evaluate, and maintain critical data in a highly organized manner including lab notebook maintenance with good documentation practices. | 1/22/2021 |
| 9438 | Bluebird Bio Cambridge, MA Associate Scientist II BS in Cell Biology, Immunology, Biochemical Engineering, or Related Exp: 0+ Years |
The focus of this position is to work on determining functional understanding and characterization of drug product manufacturing processes for stem cell therapies. Responsibilities: Performing experiments involving the isolation, transduction, expansion, and cryopreservation of gene-modified cells for treatment severe genetic diseases. Executing complex technical work related to stem cell biology, including cell isolation, viral gene transfer, tissue culture, PCR, flow cytometry, and other immunological assays. Working with all aspects of mammalian cell culture, including media and buffer preparation, culture initiation, propagation, and cryopreservation of cells, including primary human cells. Successfully completing general laboratory tasks including equipment maintenance. Maintaining accurate and reliable record keeping including database management, batch records, notebooks, and all other pertinent documentation. | 1/22/2021 |
| 9439 | Bluebird Bio Durham, NC Quality Control Analyst BS in Microbiology or Related Exp: 1-2 Years |
Responsibilities: Perform cGMP Microbial testing (Environmental Monitoring, Compressed Gas sampling and testing, and water collection). Follow procedures and provide direction on deviations from the norms. Review and evaluate raw data from a peer or technical review level of all analytical methods, as well as sample authorization. Implement and support operational systems (equipment/instrument maintenance/calibration, equipment alarm monitoring, sample handling/tracking, data integrity/control, cGMP documentation, LIMS, laboratory audit, and method training). Participate in providing the necessary information for regulatory filings and inspections. | 1/22/2021 |
| 9440 | Bluebird Bio Cambridge, MA Associate Scientist, Molecular and Vector Biology BS in Biological Sciences Exp: 0+ Years |
Responsibilities: Working in a cross-functional environment to develop and create new technologies enabling new lentivirus therapies. Applying technical expertise to develop next generation in vitro assays. Engineering LVV to transduce novel cell types to create new cell therapies and treat new classes of diseases. | 1/22/2021 |
| 9441 | Blueprint Medicines Cambridge, MA Clinical Study Associate I/II - Clinical Operations BS in Relevant Discipline Exp: 1-2+ Years |
Responsibilities: Participates in the day to day supervision of clinical trial execution, with a focus on site start up, patient enrollment, monitoring, and data flow metrics from the clinical sites, CROs and central labs. Supports complex clinical trial activities in support of the Clinical Study Manager and other team members. Prepares study documents (i.e. consent forms, site instructions, study specific materials such as the Manual of Operations, Pharmacy binder, etc.). Ensures tracking of essential documents are received and filed in the TMF, reviews site documents for accuracy; provides clinical team support with TMF filing and management. Ensures tracking of patient status throughout the study at investigative sites. Tracks and monitors sample collection, central laboratory reporting, and manages laboratory testing schedule. Assists with laboratory vendor management and liaises with the CRO and clinical trial sites to ensure appropriate sample handling, shipment and result reporting. | 1/22/2021 |
| 9442 | Boston Scientific Arden Hills, MN Quality Analyst II MS in Relevant Discipline Exp: 0-2 Years |
In this role you will provide support to the Arden Hills Operations teams (with additional cross-site support to other Rhythm Management locations) in processing and maintaining system level product containment activities as a part of the Non-Conforming Materials quality system sub-process for Arden Hills. This includes the collection, and analysis of complex query data from several systems (SAP, MES, SAP Business Objects) to help guide the engineering team to document system containment that can be effectively implemented and managed. This resource will serve as a Containment Administrator by assisting in the execution and tracking of assigned deliverables for Product Containment activities. In addition, where appropriate this resource will assist the Quality System stewards and project managers in the execution of projects designed to improve the compliance, efficiency, harmonization, and effectiveness of the BSC Quality System. | 1/22/2021 |
| 9443 | Boston Scientific Maple Grove, MN Design Assurance Engineer I Job BS in Scientific or Engineering Field Exp: 0-2 Years |
The Design Assurance Engineer I is a quality engineer that supports medical device product development from concept through commercialization as a member of the Compliance and Continuous Improvement team.ﾠ This position will work with high-performance, cross-functional teams to optimize and maintain quality systems procedures, tools, and guidance that support the execution of Design Control, Risk Management, and Post-Market Surveillance within Interventional Cardiology.ﾠﾠ | 1/22/2021 |
| 9444 | Boston Scientific Arden Hills, MN Regulatory Document Control Specialist II Job BS in Relevant Discipline Exp: 1-2 Years |
This role will support key internal customers, Cardiac Rhythm ManagementﾠResearch & Developmentﾠprojects as well as strategic projects within the IDS (Information Documentation Services) department. Maintains and implements change management system in support of quality systems and practices to meet BSC, customer and regulatory requirements. Serves as a quality representative contact on own area of expertise and to support the manufacturing facility. | 1/22/2021 |
| 9445 | Boston Scientific Arden Hills, MN Electronic Technician II BS in Electrical or Mechanical Engineering Exp: 1+ Years |
The Electronic Technician performs skilled-level testing, maintenance and repair. The testing is performed on PCB level and finished product, using protocols and direction from Engineering staff. Responsibilities: Maintains and repairs electronic equipment. Evaluates and documents custom designed systems. Uses protocols and procedures to build and perform test and repairs. Documents test changes and test results in electronic format. Consults with team members for both new and existing test systems. Advises design engineers on issues that may occur when performing the testing. Track time, materials, and other job-related data. | 1/22/2021 |
| 9446 | Boston Scientific Marlborough, MA Product Labeling Specialist II BS in Scientific or Technical Discipline Exp: 0-3 Years |
Responsibilities: Creates, reviews, and reproduces product text for medical product labeling. Ensures all text for product labeling, Instructions for Use, and equipment manuals meet all required legal, regulatory, clinical, marketing, packaging engineering, manufacturing (contract and internal) and R&D requirements through the use of corporate labeling guidelines and SOPs. Design labeling materials according to specific parameters to meet the requirements of the corporate master brand (labels, Instructions for Use artwork/layout, etc.). Establishes needs for translations as defined in the marketing/product specifications and manages the process for translation completions and reviews for project assigned. Coordinates proofing of various Labeling materials (Instructions for Use, Manuals, and Labels) using manual and electronic proofing tools. Coordinates reviews with all disciplines of various product labeling materials. Manage multiple projects concurrently, while complying with good manufacturing practices (GMPs), regulatory, quality systems standards and labeling requirements. | 1/22/2021 |
| 9447 | Boston Scientific Maple Grove, MN QA Engineer/Data Scientist II MS in Computer Science, Statistics, Data Science, or Related Exp: 0-2 Years |
The successful candidate will be a project leader in the improvement of the Peripheral Interventions (PI) division global product performance analytics, interacting with all divisions and partner functions to ensure alignment and the best predictive methods are employed. This role will have technical leadership responsibilities for the development and implementation of analytical programs improving compliance and product performance. The individual will be a key participant in the establishment and implementation of a Data Analytics Strategy.ﾠ | 1/22/2021 |
| 9448 | Boston Scientific Maple Grove, MN R&D Engineer II Job MS in Chemnical Engineering, Material Science, or Polymer Science Exp: 0+ Years |
This R&D Engineer II will be an extended team member in new product development for a strategic product in our Interventional Oncology business.ﾠ This role will involve complex technology and ability to be at forefront of research and development for our customer-centered approach to serve cancer patients. | 1/22/2021 |
| 9449 | BrainLab Providence, RI Clinical Specialist BS in Biomedical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 Years |
Responsibilities: Provide on-site consulting, guidance and assistance to physicians and OR personnel by evaluating options and problem-solving during surgery in order to maximize IGS (ImageﾠGuided Surgery)ﾠproduct efficiency and usage. Analyze, resolve and repair product issues through detailed analysis and utilization of engineering expertise. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of IGS products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels, and working to increase revenue via the sale of spare parts, upgrades, etc. Work closely with the Senior Application Consultant, Area Account Manager, Key Account Manager and Marketing Manager on market transparency, upgrade initiatives and R&D projects. | 1/22/2021 |
| 9450 | BrainLab Houston, TX Application Consultant BS in Biomedical Engineering, Biomechanical Engineering, Clinical Engineering, or Nursing Exp: 1-3 Years |
Brainlab's Application Consultants perform custom installations and provide consultation and guidance for customers utilizing the company's product portfolio. Responsibilities: Conduct on-site clinical evaluations for new and existing customers to demonstrate the use of products and services to increase the frequency and quality of IGS (Image Guided Surgery) product usage. Provide on-site consulting, guidance, and assistance to physicians and OR personnel by evaluating options and problem-solving during surgery in order to maximize IGS (Image Guided Surgery)ﾠefficiency and usage. Lead installations and establish functionality at new and existing customer sites. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of IGS (Image Guided Surgery) products and services. | 1/22/2021 |
| 9451 | BrainLab Hoboken, NJ Application Consultant BS in Biomedical Engineering, Biomechanical Engineering, Clinical Engineering, or Nursing Exp: 1-3 Years |
Brainlab's Application Consultants perform custom installations and provide consultation and guidance for customers utilizing the company's product portfolio. Responsibilities: Conduct on-site clinical evaluations for new and existing customers to demonstrate the use of products and services to increase the frequency and quality of IGS (Image Guided Surgery) product usage. Provide on-site consulting, guidance, and assistance to physicians and OR personnel by evaluating options and problem-solving during surgery in order to maximize IGS (Image Guided Surgery)ﾠefficiency and usage. Lead installations and establish functionality at new and existing customer sites. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of IGS (Image Guided Surgery) products and services. | 1/22/2021 |
| 9452 | BrainLab Salt Lake City, UT Clinical Specialist BS in Biomedical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 Years |
Clinical Specialists work with client's physicians and other medical personnel to provide clinical guidance and product support in real time during surgery. Responsibilities: Provide on-site consulting, guidance and assistance to physicians and OR personnel by evaluating options and problem-solving during surgery in order to maximize IGS (ImageﾠGuided Surgery)ﾠproduct efficiency and usage. Analyze, resolve and repair product issues through detailed analysis and utilization of engineering expertise. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of IGS products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. | 1/22/2021 |
| 9453 | Bruker Corporation Hayward, CA Research Associate BS/MS in Molecular Biology, Genetics, Biochemistry, or Related Exp: 1-3 Years |
Responsibilities: Performs assays and lab procedures related to Multiplex IHC assays including fluorescent imaging, antibody staining, PBMC isolation, and tissue sectioning according to SOPs using appropriate laboratory techniques. Performs various molecular biology techniques including but not limited to nucleic acid purification and QC analysis. Maintains laboratory notebooks, SOP documents, and computer databases. Performs sample intake and accessioning. Manages, monitors, and maintains equipment, facilities, and supplies. This will include routine handling and lifting of laboratory supplies and bench-top equipment. Works in a professional and collaborative manner with coworkers and customers. Provides operational support for testing activities including reagent preparation, cleaning activities, and equipment maintenance. | 1/22/2021 |
| 9454 | Bruker Corporation San Jose, CA Engineer, Application Scientist BS/MS in Materials Engineering, Chemical Engineering, Chemistry, or Physics Exp: 0+ Years |
Responsibilities: Provides technical expertise through sales presentations, product demonstrations, installation and maintenance of company products.ﾠAssists the sales staff in assessing potential application of company products to meet customer needs and preparing detailed product specifications for the development and implementation of customer applications/solutions.ﾠMay build an application based on customer requirements to demonstrate feasibility of the application, often requiring rapid prototyping and/or product demo for client.ﾠMay provide software development and consultation to prospective users and/or product capability assessment and validation.ﾠSupport of the core technology, engineering and production teams in qualification of the new technologies, algorithms, methodologies, software and hardware features. | 1/22/2021 |
| 9455 | Essity Barton/Cherokee, AL Process Engineer BS in Chemical/Paper Science, Mechanical, Electrical, or Industrial Engineering Exp: 1+ Years |
This role serves as the day-to-day owner of the machine processes and process control systems for the plant. Owns and manages the development of troubleshooting skills of the manufacturing professionals. Acts as a subject matter expert for the machine processes. Participates and/or leads in Continuous Improvement projects. Helps to identify and support projects that will improve productivity, waste, quality and safety performance on a long term basis. | 1/22/2021 |
| 9456 | Novartis Millburn, NJ Production Technician BS in Engineering or Scientific Discipline Exp: 0+ Years |
The Production Technician plays an active role in daily production of Lutathera as well as setup and preparation of instruments and equipment. Due to the nature of the process (radioactive) this role requires basic proficiency, ownership of the process and understanding of radiation safety standards. | 1/22/2021 |
| 9457 | Novartis Cambridge, MA Computational Biologist, Oncology Data Science MS in Computational Biology, Bioinformatics, Data Science, or Related Exp: 1+ Years |
Responsibilities: Working closely with interdisciplinary teams of wet lab and dry lab collaborators to analyze and interpret high-dimensional biological data (e.g., bulk RNAseq, single-cell RNAseq, CRISPR screens, proteomics) to inform critical project decisions. Implementing and developing state-of-the-art computational methods and data mining strategies to address key challenges in oncology drug discovery. Identifying novel drug targets on cancer cells, immune cells, and/or other cell types in the tumor microenvironment. Deepening our understanding of drug resistance and strategies to overcome it. Formulating testable biological hypotheses and collaborating in the design of rigorous preclinical experiments. Driving forward multi-disciplinary collaborations and projects, and establishing them as needed. | 1/22/2021 |
| 9458 | Novartis Cambridge, MA Vivarium Operations Technician BS in Relevant Discipline Exp: 0+ Years |
Vivarium Operations (VO), as a function of Comparative Medicine (CM), provides high quality animal care to laboratory animals enrolled in studies within 14 disease area teams within NIBR. VO is looking for the ideal candidate to fill an entry level vivarium operations technical position responsible for maintaining the health and welfare of laboratory animals and supporting research by doing daily health and checks and husbandry, organizing facility data and records, and helping with all daily facility needs. This position will closely collaborate with the CM organization and NIBR disease area teams within our multi-building, multi-discipline, multi-species research program, focusing on the zebrafish with some rodent work as well. | 1/22/2021 |
| 9459 | Novartis Carlsbad, CA Associate Scientist, High Dimensional Flow Cytometry MS in Scientific Discipline Exp: 0-4 Years |
As an Associate Scientist at Navigate, you will help to design, create, execute, and troubleshoot Flow cytometry based procedures and assays. You will be expected to exhibit moderate to high level of independence while working on multiple projects including contributing to the launch of new platforms/assays. Candidates must demonstrate critical thinking, initiative and effective stakeholder management in the execution of their projects. | 1/22/2021 |
| 9460 | Novartis Cambridge, MA Research Scientist - Sickle Cell Disease, Hematology MS in Biology, Chemistry, or Pharmacology Exp: 0+ Years |
Responsibilities: Will assume a crucial role in the development of novel therapeutic concepts and will contribute at all stages of a project, from inception, early project validation, optimization, candidate selection and through to early clinical development of novel medicines for patients with sickle cell disease. Will work collaboratively with other specialists to develop project strategy, identify key drug discovery issues, propose and implement creative solutions, execute and guide teams to success and decision points. He/she will conduct early research to develop in vivo targeted gene delivery strategies for Sickle Cell Disease. | 1/22/2021 |
| 9461 | Novartis Cambridge, MA Scientific Associate I, Veterinary Medicine BS in Scientific Discipline Exp: 0+ Years |
VM is looking for the ideal candidate to fill an entry level veterinary technical position responsible for maintaining the health and welfare of laboratory animals and supporting research by triaging emergencies, treating common clinical conditions in laboratory animals, and recognizing study-related clinical trends. This position will closely collaborate with the CM organization and NIBR disease area teams within our multi-building, multi-discipline, multi-species research program. | 1/22/2021 |
| 9462 | Novartis Carlsbad, CA Associate Clinical Laboratory Scientist BS in Scientific Discipline Exp: 0+ Years |
Responsibilities: Works in a GMP/GCP/GLP/CLIA regulated environment and is responsible for following all applicable regulations. Assist in activities related to validation of new laboratory tests, new instrumentation, and new laboratory software. Perform all clinical specimen testing (pre-analytical/analytical procedures) as assigned under supervision. Use LIMS to perform sample management, testing worklists, enter test results and QC data. Adheres to established turn-around-times while maintaining highest quality of test results. | 1/22/2021 |
| 9463 | Cairn Biosciences San Francisco, CA Research Associate/Senior Research Associate MS in Cell Biology, Neuroscience, Biochemistry, Bioengineering, or Related Exp: 1+ Years |
Cairn is seeking a talented, highly-motivated and detail-oriented Research Assistant/Associate who is committed to delivering scalable innovations in quantitative live cell biology as an integral member of a tight-knit multidisciplinary team. The successful candidate will play a key role in the ongoing development of Cairnﾒs next-generation drug discovery platform. | 1/22/2021 |
| 9464 | BioFire Diagnostics Salt Lake City, UT Quality Control Supervisor BS in Biological, Engineering, or Chemical Field Exp: 1+ Years |
The QC Supervisor supervises the daily work of the Technologists in the Reagent QC group. This includes oversight of the employees, processes, and product while providing support to their team. Ensures daily and weekly tasks are completed including decontamination and housekeeping, participation in the swabbing program, and overseeing the processing of IVD product. Supervises performance of team members to ensure personnel matters are addressed and works with the Manager to resolve issues or pursue corrective action as necessary. Interacts with QA, BioMath, Manufacturing, Incoming QC, Engineering, Transfer Support, IQC, Software, Facilities, and other applicable departments to resolve product, process, and equipment issues. Creates and maintains a daily schedule of work performed by individuals to help manage capacity effectively and ensure rotation of job tasks. Ensures safety of Technologists working in a laboratory environment. | 1/13/2021 |
| 9465 | BioFire Diagnostics Salt Lake City, UT Clinical Applications Specialist I/II BS in Biological Sciences, Molecular Biology or Microbiology Exp: 0+ Years |
Clinical Applications Specialists (CAS) serve as product experts to provide applications and technical support for all clinical product applications. This applications and technical expertise is used to support sales growth through delivering exceptional technical support. CAS ensure a high degree of customer satisfaction and loyalty to BioFire products as the primary contact for system applications, technical support, troubleshooting of instrument, reagent, and software issues. CAS also manage the complaint handling process to ensure the timely, accurate resolution of customer complaints, which often involves working closely with other groups, such as Post Market Surveillance, Regulatory, R&D, Manufacturing, Engineering, Systems Integration, Legal, Service, and Instrument Production. The CAS support BioFire (BFDX) customers, distribution partners, BioMerieux (BMX) subsidiaries/distributors, BMX Global Customer Support, and the BFDX Sales network (Sales Managers, Clinical Implementation Managers, Corporate Account Managers, Field Applications Specialists, etc.). CAS also play an active role and serve as a customer advocate during product development, improvement, transfer, and release to ensure that the customer’s perspective is represented. | 1/13/2021 |
| 9466 | BioFire Diagnostics Salt Lake City, UT Global Medical Affairs Epidemiologist I MS in Public Health, Biostatistics, Population Health, or Related Exp: 1+ Years |
The Epidemiologist’s primary responsibility is to provide expert methodological guidance and support for the Global Medical Affairs team. This will include review of scientific study protocols for externally and internally developed studies to support the clinical and economic value of BioFire in vitro diagnostic products. Additionally, other responsibilities include contributing to the execution of internally developed studies. The Epidemiologist must stay up-to-date with the scientific and medical knowledge related to infectious disease and actively participated in the design of Health Economic and Outcome Research (HEOR) to ensure that the results of the studies will better inform medical practice related to BioFire’s products. Position may manage Clinical Research Associates or Clinical Coordinators. | 1/13/2021 |
| 9467 | BioFire Diagnostics Salt Lake City, UT Lab Technologist - Quality Control I/II AS/BS in Life Science or Related Exp: 0+ Years |
Responsibilities: Perform all work in compliance with company policy and within the guidelines of Biofire Diagnostic’s Quality System. Responsible for performing quality control testing on incoming reagents use in Film Array. Responsible for maintaining supply stocks as well as coordinating instrument/equipment repairs as necessary. Responsible for all pipet calibrations and the Artel system calibration. Responsible for all Film Array Contamination monitoring, collection, setup and reporting. Responsible for all other swab set up and reporting. Responsible for maintaining all QC charts. Responsible for maintaining the QC area clean and contamination-free. Responsible for coordinating repeats. | 1/13/2021 |
| 9468 | BioFire Diagnostics Salt Lake City, UT Regulatory Affairs Assistant BS in Scientific Discipline Exp: 0+ Years |
Responsibilities: Work cross-functionally with regulatory specialists, key internal departments, and external regulatory bodies to support product submissions. Coordinate and collect information from various departments (e.g., R&D, Clinical, QA, Engineering, etc.) to support regulatory projects, as needed. Coordinate and respond to requests from global regulatory agencies. Assist with regulatory assessments and strategies for proposed change notifications international jurisdictions. Process notarization & legalization of registration documents. Maintain and organize department spreadsheets. | 1/13/2021 |
| 9469 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II BS/MS in Biology, Molecular Biology, or Biotechnology Exp: 1+ Years |
The selected candidate will perform general lab duties, design and conduct experiments, primarily PCR, collect and analyze data, and keep an accurate record of all work done in accordance with the quality system. The ideal candidate will have some problem solving skills and ability to work with minimal instructions on routine work and general instructions on all new assignments. This position reports to the Lab Supervisor or a Scientist. | 1/13/2021 |
| 9470 | BioMérieux Durham, NC Biochemist MS in Biochemistry or Closely Related Exp: 1+ Years |
As part of the Industrialization Analytical department, the Associate Process Scientist (Biochemist) will perform projects to support the manufacturing of BACT/ALERT® Culture Media products. Within this role the Associate Process Scientist will be required to interface with Manufacturing, Quality Control, Quality Assurance, R&D, Purchasing, Supply Chain, and other functions as required in order to ensure successful project achievements to facilitate quality production that meets on-time customer demands. | 1/13/2021 |
| 9471 | BioMérieux Durham, NC Learning and Development Specialist BS in Scientific Discipline Exp: 1+ Years |
This position is responsible for assessing, developing and maintaining effective training materials for BMX sites regionally and globally as needed. The learning and development specialist will assist the management team in maintaining regulatory compliance with training requirements as documented in the Company’s quality system. | 1/13/2021 |
| 9472 | BioMérieux Saint Louis, MO Media Technician BS in Biology or Chemistry Exp: 1+ Years |
The primary purpose of this position is to prepare complex chemical media and/or sub components, dispensing system setup/verifications, insuring timely delivery of high quality product to Card production, being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department | 1/13/2021 |
| 9473 | BioMérieux Saint Louis, MO Global Medical Affairs Research Associate MS in Health Sciences or Related Exp: 1-3 Years |
Responsibilities: Serve as primary contact between bioMérieux and site investigators. Work with bioMérieux legal team and study sites to execute research agreements. Manage all study documentation. Monitor project execution according to timeline and budget set forth in study contract. Perform site visits as needed. Manage study supplies and reagents, and site payments. Track all study milestones and deliverables, including any publications. Provide updates to the PPLS team on the status of studies. Assist the PPLS team with other activities as needed. | 1/13/2021 |
| 9474 | Biogen Research Triangle Park, NC Engineer I, Process BS/MS in Relevant Scientific Discipline Exp: 0-2 Years |
The position provides responsible engineering support for GMP (Good Manufacturing Practice) equipment in a Cell Culture and/or Purification area including bioreactor, perfusion, chromatography, centrifugation, UF/DF, solution preparation and filtration operations. Designs, specifies, installs, and commissions new equipment and provides engineering technical support and troubleshooting for cell culture or purification processing equipment including associated automation. Engagement and support of process tech transfers is required to ensure manufacturing equipment meets process requirements. Investigates process or equipment failures and implements changes to avoid future occurrences. Provides support for new equipment evaluations and process improvement studies. Investigates equipment failures and implements changes to avoid future occurrences. Provides support for site and global regulatory inspections, as needed. | 1/13/2021 |
| 9475 | Biogen Cambridge, MA Bioinformatics Engineer BS/MS in Computational Biology, Bioinformatics, Bioengineering, or Computer Science Exp: 1-3 Years |
This role will fall under the Genome Technology and Computational Sciences group which provides scientists with cutting-edge computational informatics and analytics tools and services in support of research and early development. The team has the technical depth, agility and great motivation to solve scientifically demanding problems. The Bioinformatics Engineer will be involved in the development of bioinformatics pipelines, R Shiny applications, and visualization tools. This position will also be responsible for developing bioinformatics tools and implementation of laboratory information systems. | 1/13/2021 |
| 9476 | Biogen Cambridge, MA Associate Scientist II, Gene Therapy - Cell Line Technology BS in Biology Exp: 0-2 Years |
The candidate will capitalize on their skills in molecular biology to engineer stable cell lines and viral vectors to support development of gene therapy manufacturing platforms. A background in cell biology, bioengineering, or microbiology is highly valued. Experience with molecular cloning, viral vector engineering, and high-throughput mammalian cell culture is preferred. The successful candidate will work efficiently with team members and independently to plan, conduct, analyze, and document experiments to drive innovation in a cutting-edge modality. | 1/13/2021 |
| 9477 | Biogen Cambridge, MA Associate Scientist III, Protein Drug Product Development MS in Chemical Engineering, Biochemical Engineering, Biotechnology, or Related Exp: 0-2 Years |
As a member in Biogen’s Protein Drug Product Development team, the candidate will be primarily responsible for supporting formulation, process, and container development of parenteral drug products. This includes an emphasis on process and formulation development along with associated analytics. The ability to work independently, collaboratively in an innovative, agile manner are key attributes for the successful candidate. The individual is expected to present findings and/or results internally within the department and to external stakeholders, and author study reports. The role will involve developing, assessing, and implementing new technologies along with developing platforms, aligned with the department’s long-range technology development plans | 1/13/2021 |
| 9478 | Biogen Cambridge, MA Production Operation Specialist II, External Manufacturing BS in Quality, Engineering, Supply Chain, or Related Exp: 1-2 Years |
The Production Operations Specialist maintains day-to-day Oracle production activities and works closely with the CMO Virtual Plant Teams to maintain systems and production timelines. Responsibilities: Execute external production-related transactions in Oracle in a timely and accurate manner. Generate purchase orders and perform invoice reconciliation. Ensure production readiness (e.g. authorizations-to-manufacture). Create and update production batches in alignment with production planning (updated due dates, planned dates, and actual dates for production and release steps). Align proactively with CMO Virtual Plant Teams regarding ongoing production, priority batches and production challenges. Leads or supports continuous improvement projects, metrics reporting, process documentation and training. | 1/13/2021 |
| 9479 | Biogen Cambridge, MA Engineer II, Device Design and Process Development MS in Engineering Exp: 0-2 Years |
Biogen is seeking a qualified candidate for the role of device design and process development Engineer II in the Medical Devices & Packaging Department. The position will lead the design and process development of patient-centric, safe, reliable, and innovative devices. Beginning with continuous research of cutting-edge technology to develop delivery systems integrated with the pipeline. Effectively and efficiently bring optimized products to market through rigorous science and engineering by leveraging external partnerships in collaboration with internal Human Factors, Packaging, Manufacturing Science, Engineering, Quality and Regulatory Affairs etc. | 1/13/2021 |
| 9480 | Biogen Cambridge, MA Associate Scientist II, Cell Culture Development, Gene Therapy BS/MS in Bioengineering, Biochemical Engineering, Biochemistry, or Related Exp: 0-2 Years |
Biogen is presently looking to fill an Associate Scientist II position within its Gene Therapy Process Development department. Candidate must be motivated and innovative with exceptional analytical and communication skills. Responsibilities: Assist with experimental design and execute laboratory experiments with minimal guidance. Perform independent data recording and analysis. Troubleshoot in-lab activities. Work with small- and large-scale operations depending on need. Document development work in concise reports and provide project updates in written and oral presentations. Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside vendors/suppliers. | 1/13/2021 |
| 9481 | BioLegend San Diego, CA Quality Control Associate BS in Scientific Discipline Exp: 1+ Years |
BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. This position will also perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. | 1/13/2021 |
| 9482 | BioLegend San Diego, CA Biochemist - Process Development (Conjugation) BS in Biochemistry, Bio-Organic Chemistry, or Related Science Exp: 1+ Years |
The Biochemist for the Process Development team will work to support customer request including customer conjugation and other non-catalog products. The responsibilities of this position will also involve development new products related to immunology research reagents and will support the antibody manufacturing team by troubleshooting and optimizing processes for continuous improvement. And more job duties are preferred including exploring new technologies and developing new Standard Operating Procedures (SOPs) under the guidance of the Research Scientists. | 1/13/2021 |
| 9483 | BioLegend San Diego, CA Biochemist - Purification BS in Biology, Chemistry, or Related Exp: 0-1 Years |
The Biochemist will be an integral member of a team, that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform column chromatography, troubleshooting of problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 1/13/2021 |
| 9484 | BioLegend San Diego, CA Research Associate - Protein Purification BS in Biological Sciences Exp: 0+ Years |
This position is responsible for developing recombinant protein research products in Molecular Cellular Biology group by using cutting-edge synthetic biological technology. The duties include preparing buffer solutions and E. Coli cell culture media, performing bacterial cell cultures, and purifying recombinant proteins with affinity tag, performing protein characterization according to standard operating procedures. This position offers a significant opportunity for learning molecular biology techniques and career growth in biotechnology industry. | 1/13/2021 |
| 9485 | BioLegend San Diego, CA Research Associate - Recombinant Protein & Molecular Cloning BS in Biological Sciences Exp: 0+ Years |
This position is responsible for developing cutting edge recombinant protein research products in Molecular Cellular Biology group. The research associate will be involved on developing a new line of recombinant protein products by supporting other team members. The duties include preparing buffer solutions and cell culture media, performing PCR and DNA purification according to standard operating procedures, performing bacterial and mammalian cells cultures, and purifying recombinant proteins with affinity tag. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 1/13/2021 |
| 9486 | BioLegend San Diego, CA Research Associate - Diagnostics BS in Life Sciences Exp: 1+ Years |
This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report. | 1/13/2021 |
| 9487 | BioLegend San Diego, CA Research Associate - Biomarker Immunoassay BS in Biology or Chemistry Exp: 1-3 Years |
This position is responsible for making custom multiplex immunoassay products in the Biomarker Immunoassay group. The Research Associate will be working with an experienced scientist and will be involved in all aspects of custom assay production processes including planning, manufacturing, testing, troubleshooting, optimizing and product order fulfilment. The customized products are an indispensable part of our bead-based immunoassay product portfolio and are complementary to the on shelf products. These products may allow simultaneously detection of up to 13 important biomarkers for inflammatory diseases, cancer, cardiovascular disease or neuron degenerative disease and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experiences in a fast-paced biotech industrial environment | 1/13/2021 |
| 9488 | BioPharma Services Saint Louis, MO QC Data Reviewer BS in Science or Healthcare Related Discipline Exp: 1-2 Years |
Responsibilities: Review study files after completion and ensure that they are accurate and legible according to protocol, SOPs and regulations. Ensure all prepared study source documents and/or forms are in accordance to protocols, SOPs and regulations. Review all other study related documentation: medical screening files, pharmacy labels and files, final report tabulations and PK STAT input and output as assigned. Observe, on a random basis, clinical procedures during the conduct of studies, sample bundling and shipping process. Provide reports of the reviewed data to relevant personnel/department.Responsibilities: Review study files after completion and ensure that they are accurate and legible according to protocol, SOPs and regulations. Ensure all prepared study source documents and/or forms are in accordance to protocols, SOPs and regulations. Review all other study related documentation: medical screening files, pharmacy labels and files, final report tabulations and PK STAT input and output as assigned. Observe, on a random basis, clinical procedures during the conduct of studies, sample bundling and shipping process. Provide reports of the reviewed data to relevant personnel/department. | 1/13/2021 |
| 9489 | BioRad Irvine, CA Research Associate I/II BS/MS in Related Life Science or Technical Discipline Exp: 0+ Years |
Bio-Rad is looking for Research Associate to work in the R&D Hematology Development group. The position requires a working knowledge of laboratory experimentation, general chemistry, and clinical chemistry. This position will assist and support the development of hematology controls. The ideal candidate will also possess abilities in data input, data processing, statistical analysis, and is comfortable working with blood, serum, urine and/or their various components. | 1/13/2021 |
| 9490 | BioRad Woodinville, WA Production Chemist I BS in Physical Sciences Exp: 0+ Years |
Manufacturing activities for BioPlex 2200 to support commercialization and development activities. Areas of responsibility could include bead coupling, conjugation, calibrator and control manufacturing, or other component manufacturing. | 1/13/2021 |
| 9491 | BioReference Laboratories Elmwood Park, NJ Genomics Technician BS in Medical Technology, Chemistry, Biology, or Related Exp: 1+ Years |
The Medical Lab Tech will perform all necessary laboratory testing in the detection, diagnosis, and prognosis of disease. The Medical Lab Tech will work collaboratively with the laboratory team to provide testing services to the clients. Additional tasks can be assigned at the discretion of the Supervisor/Manager/Director. | 1/13/2021 |
| 9492 | BioReliance Verona, WI Associate Production Scientist BS in Chemistry, Biochemistry, Chemical Engineering, or Related Exp: 0-1 Years |
Position primarily involves the safe and efficient manufacturing of API’s according to cGMP requirements. The role of Production Scientist, Associate is primarily focused on performing required production operations to support the end users and patients of the compounds produced at MilliporeSigma. These responsibilities include but are not limited to executing existing production procedures, updating ancillary documents, and maintaining the safety and quality of the manufacturing environment. | 1/13/2021 |
| 9493 | BioReliance Saint Louis, MO Associate Scientist BS in Chemistry, Biochemistry, Chemical Engineering, or Biology Exp: 6+ Months |
The Associate Scientist will evaluate immunoassay products according to established protocols and contribute to the support functions to maintain group and department operations. Responsibilities: Safely perform operations to meet quality expectations. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). Provide complete and accurate records consistent with quality guidelines. Perform testing of established processes and procedures. Participate in pre-audit activities and on department teams. Participate in process improvements under the guidance of a Supervisor or Scientist. Notify Supervisor of any deviations to established processes or procedures. | 1/13/2021 |
| 9494 | BioReliance Jaffrey, NH Quality Technician II/III BS in Biology, Chemistry, or Related Exp: 0+ Years |
This role will perform a variety of testing, media and solution preparation, troubleshooting, and diagnostic tasks to ensure compliance with quality standards. The individual shares responsibility for lab equipment maintenance, housekeeping and other lab support functions while ensuring compliance with all established quality requirements, standards and maintains the lab in an audit-ready state. The candidate will demonstrate the ability to work well in a team environment and to exhibit sound judgment in non-routine situations. Willingness to support challenging goals to achieve superior performance are a must. Individual will anticipate and suggest solutions for risks to compliance and efficiency. Candidate will provide support for continuous improvement projects (validations, change control, process improvements). Primary commitment to safety and product quality by maintaining compliance to the Quality policy and other documented safety and quality processes and procedures. | 1/13/2021 |
| 9495 | BioReliance Saint Louis, MO Scientist I: Bioprocesssing R&D Cell Line Development and Engineering MS in Life Science Discipline Exp: 1+ Years |
The successful candidate will be part of a multidisciplinary group of scientists responsible for the design and development of host cells for the biopharmaceutical industry. You will provide technical support for multiple projects, being responsible for design and execution of experiments, interpreting results, and determining next steps alongside the project team/lead. This role involves working with mammalian cell/tissue cultures and requires proficiency in the use of aseptic techniques. A good understanding of biochemistry, molecular biology, and genetic engineering techniques is necessary. Responsibilities also include maintenance of a detailed laboratory notebook, contribution to lab support functions (cleaning, equipment maintenance, reagent preparation, etc), and adherence to all MilliporeSigma systems, policies, and procedures. You will be required to read and understand the relevant scientific literature in order to seek out new information and opportunities to advance the team's technologies, products, and services. You may have direct interaction with customers and may support sales and marketing colleagues by providing performance data suitable for marketing our cell line development and engineering products. | 1/13/2021 |
| 9496 | BioReliance Sheboygan Falls, WI Associate Production Scientist BS in Chemistry, Chemical Engineering, Biology, or Related Exp: 0+ Years |
The Associate Production Scientist will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Responsibilities: Perform operations to meet quality expectations. Ensure quality throughout the process. Assure you are adequately trained to perform tasks/assignments. Perform routine assays, processes and/or unit operations. Complete the volume of work required to achieve group/departmental goals and meet deadlines. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). Communicate the status of operations and bring deviations to the attention of supervisor. | 1/13/2021 |
| 9497 | BioReliance Rockville , MD Associate Scientist III MS in Scientific Discipline Exp: 1+ Years |
As an associate scientist/molecular biologist within our Next Generation Sequencing (NGS) group in our Rockville, Maryland facility, your activities will support commercial biosafety testing within the organization, specifically using NGS platforms. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/ documentation and ensure all documentation fulfills generally accepted professional/ industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position. | 1/13/2021 |
| 9498 | BioReliance Temecula, CA Associate Manufacturing Scientist BS in Life Sciences Exp: 1+ Years |
Under direct supervision, perform routine laboratory operations associated with the manufacture and packaging of cell culture media and reagents for Life Science business unit resulting in customer satisfaction. Partner with R&D, Technical Transfer, Planning, Production, Quality Control, and Distribution to manufacture and assemble products in final configuration to meet customer needs. | 1/13/2021 |
| 9499 | LGC Biosearch Technologies Charleston, SC Production Chemist BS in Chemistry Exp: 0+ Years |
This is a production job in which the chemist is expected to produce standards quickly and accurately using weighing, syringing, and pipetting techniques. Packaging is also involved which includes putting products in bottles, ampules, or another specified container and applying labels for clients. | 1/13/2021 |
| 9500 | LGC Biosearch Technologies Petaluma, CA CPG Manufacturing Technician I BS in Chemistry Exp: 0-2 Years |
This role is responsible for the manufacturing of Controlled Pored Glass (CPG) materials by following established and robust protocols. CPG material manufacturing would include amine and nucleoside modification of native CPG at various angstrom sizes as well as modification with proprietary dyes and quenchers. The CPG Tech I will also be responsible for the manufacturing, upkeep, and repair of basic CPG reactors used in these processes. | 1/13/2021 |
| 9501 | LGC Biosearch Technologies Novato, CA GMP Manufacturing Technician I BS in Relevant Discipline Exp: 0+ Years |
The GMP Manufacturing Technician I position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. | 1/13/2021 |
| 9502 | LGC Biosearch Technologies Petaluma, CA Diagnostic Oligo Manufacturing Technician I BS in Relevant Discipline Exp: 0+ Years |
The Diagnostic Oligo Manufacturing Technician I position is responsible for manufacture of GMP-grade oligonucleotides for customers preforming mission critical diagnostic testing and research. Production laboratories include DNA synthesis, HPLC purification, mass spectrometry, and formulation. Technicians are expected to perform manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. | 1/13/2021 |
| 9503 | LGC Biosearch Technologies Petaluma, CA Oligonucleotide Production Technician I BS in Life Science or Chemistry Exp: 0+ Years |
The Oligo Production Technician I is responsible for performing day to day production activities in the custom oligonucleotide (oligo) production lab. Production activities will be performed in a timely fashion and in compliance with company procedures. Responsibilities: Performs all assigned job functions per documented procedures or as directed by the supervisor/manager. Perform oligonucleotide synthesis/purification according to established procedures. Tracking and updating synthesis/purification status. Proficiency using automated and manual pipettes. Demonstrated ability to perform basic chemistry equations. Basic knowledge and capable of operation of instruments in immediate work area. Performs basic daily equipment and lab maintenance tasks. Maintain a clean and orderly maintenance of equipment used in manufacturing. | 1/13/2021 |
| 9504 | August Bioservices Nashville, TN Lab Research Technician, Protein Science BS in Biology, Chemistry, Biochemistry, or Related Exp: 1-2 Years |
The Lab Research Technician will work within a team of highly motivated laboratory staff and scientists. This role will have a significant impact on the team’s progress through direct involvement in specific projects and support the daily operations in the Research Services lab. The chief role of this employee is to assist senior laboratory personnel with administrative lab duties and with protein expression and purification activities. The job involves performing sanitation and sterilization of labware, assisting with inventory management & equipment maintenance. The successful candidate should also understand and be able to apply basic molecular biology and protein chemistry techniques. | 12/29/2020 |
| 9505 | August Bioservices Nashville, TN Microbiologist BS in Biology or Related Exp: 0-3 Years |
August Bioservices is seeking a Microbiologist to join their growing Analytical Development team. This is an entry-level role and recent grads are encouraged to apply. Reporting to the Manager, Analytical Development the Microbiologist will be responsible for performing environmental monitoring sampling of ISO class environments and assisting with preparation, characterization, and identification of environmental isolates. The Microbiologist will perform raw material and drug product method development and cGMP testing. | 12/29/2020 |
| 9506 | Auris Robotics & Digital Solutions Santa Clara, CA Mechanical Engineer BS in Mechanical Engineering or Related Exp: 1+ Years |
Responsibilities: As a member of the Surgical Robotics Instruments and Accessories Integration Team, you will contribute to the development and support of robotic instrumentation for a surgical robotic platform. Progress development of novel instrumentation spanning from feasibility through to product launch. Solve and perform rout cause analysis of failures seen when instrumentation are used with the Robotics Platform. Build multi-functional relationships with a multitude of different department representatives. Design and create prototypes using in-house rapid prototyping capabilities. Provide hands-on, troubleshooting, process and manufacturing support as well as designing, implementing, integrating and testing solutions in a fast pace environment with a quick development cycle. Create design solutions utilizing engineering methods with good documentation processes, releasing design documentation through an ECO process in accordance with the company design control process. | 12/29/2020 |
| 9507 | Avantor West Henrietta, NY Chemistry Technician BS in Biology, Earth Science, Environmental Science, or Related Exp: 0+ Years |
Receive, evaluate, and process living or non-living raw material into finished product. Perform quality control check on final product, adhering to departmental standards. Performance will be assessed based upon the quality of the finished product and the efficiency of its manufacture. Answer customer service questions and provide technical support. Tasks may include some warehousing, inventory control, and other indirect tasks. | 12/31/2020 |
| 9508 | Avantor Eatontown , NJ QA Inspector BS in Relevant Discipline Exp: 0+ Years |
Ensures customer and regulatory requirements have been met by inspecting incoming raw materials and review of documentation. Ensures compliance with all applicable standards and regulations (e.g., ISO 9001, ISO 13485, 21 CFR 820, 21 CFR 11, Good Manufacturing Practices (cGMPs), and Good Documentation Practices (GDPs). | 12/31/2020 |
| 9509 | Avantor Phillipsburg , NJ Chemical Technician BS in Science or Related Discipline Exp: 0+ Years |
The Chemical Technician completes procedures associated with manufacture of pilot scale batches of chemical according to established or developmental procedures. Handles raw materials (including 55 gal. drums) and process waste associated with this manufacturing. Operates various unit operations and pilot lab systems. This is a bargaining unit shift position. | 12/31/2020 |
| 9510 | Avantor Paris, KY Technician QC Lab BS in Chemistry, Biology, or Microbiology Exp: 1-3 Years |
Responsibilities: Conducts routine and non-routine chemistry and microbiological analysis of raw materials, in-process formulations and final products to established specifications. Utilizes and operates laboratory equipment and instruments according to laboratory work instruction or laboratory procedures such as pH, conductivity, UV, KF, FTIR and titrations. Ability to understand and follow Quality Control test methods or compendia methods (USP, EP, BP, JP or ACS) and EXCIPACT standard. Calculates and generates data for compliance to specifications and reports results. Performs technical review of lab data forms such as water, environmental monitoring and direct measure analysis. Calibrates and maintains lab equipment. Enters final results and raw data for tested materials or products in LIMS (Laboratory Information Management System) as needed. | 12/31/2020 |
| 9511 | Avantor Rensselear, NY Lab Support Specialist BS in Relevant Discipline Exp: 0+ Years |
Perform laboratory tests, experiments, and analyses. Closely follows standard procedures in laboratory testing, evaluating various routine assay, and in performing tasks related to stability studies, sterility testing, investigating product complaints, and evaluating new and existing product. Assists in operating manufacturing equipment and systems in a lab environment along with purification product-related operations. Follow blueprints, guidelines, and/or diagrams to ensure product specifications are met. Assist in the assembly or sub-assembly of life science products and devices. Adhere to Good Manufacturing Practices (GMPs) and Standard Operating Procedures (SOPs). | 12/31/2020 |
| 9512 | AvoMeen Ann Arbor, MI Analytical Chamist/Scientist BS/MS in Chemistry Exp: 0-5+ Years |
Responsibilities: Learn techniques spanning across the entire spectrum of analytical chemistry from wet chemistry to HPLC, NMR, Mass Spectrometry, FTIR, GC and GC-MS. Perform testing using a variety of technologies including HPLC, LC-MS, GC, GC/MS, Microscopy, FTIR and UV. Execute projects in support of client needs including product deformulation and product development, failure analysis and problem solving, impurity identification, extractable and leachable studies, and structural characterization. Follow all safety requirements including wearing appropriate personal protective equipment. Generate supporting laboratory documentation. Ensure compliance with government rules and regulations (FDA, cGMP, DEA, ICH, OSHA, etc.). Implement new equipment and processes independently, capable of conducting appropriate qualification and validation activities. | 12/31/2020 |
| 9513 | Bausch & Lomb Greenville, SC Sterilizer Operator BS in Relevant Discipline Exp: 0+ Years |
Load/unload totes and place dosimeters on product. Transfer pre-sterilized product into the APA. Unload trucks of non-sterile components from vendors and prepare them for processing while ensuring separation of sterile and non-sterile components. Place and read dosimeters using a digital micrometer and spectrophotometer. Operate Irradiator Console to set timer settings and clear faults/settings. PC Data entry to include dosimetry information and basic inventory receipt transactions in ERP Lx. Analyze and correct irradiator faults by interpreting program logic controller display indicators and repositioning switches, totes and sensors on the source pass as well as the entry and exit conveyors. Operate industrial irradiator and will load and unload components to ensure proper sterilization during irradiation operations. | 12/31/2020 |
| 9514 | Bausch & Lomb Greenville, SC Sterile Prep Operator BS in Relevant Discipline Exp: 0+ Years |
Maintain the APA in accordance with SOPs and within environmental monitoring limits by cleaning and sanitizing all equipment and rooms inside and adjacent to the APA. Document all cleaning and sanitization processes according to SOPs. Perform CIP and SIP processes for Fill Room Equipment. Install and test filters as required. Maintain the APA in orderly conditions by removing culls, performing regular inspections of the equipment and environment and using Aseptic Technique. Prepare and stock process materials for use inside the APA. | 12/31/2020 |
| 9515 | Bausch & Lomb Petaluma, CA Chemist III BS in Chemistry or Related, MS Preferred Exp: 0+ Years |
Directs and provides analytical support for research, development, and manufacturing activities. Provides high level troubleshooting and analytical method development and method validation per pharmaceutical guidelines. Ensures that laboratory work is in compliance with regulations. In-depth understanding of cGMPs, CFRs and ICH Guidances for pharmaceutical development. Prepares complex technical experimental designs and reports. Experienced in HPLC, wet chemistry analysis, and laboratory data systems. Safety minded in operation. | 12/31/2020 |
| 9516 | Baxter Round Lake , IL Senior Engineer - Reliability MS in Engineering Exp: 1+ Years |
Support plant equipment reliability through the implementation of projects improving or optimizing the computerized maintenance management systems (CMMS) and reliability systems by increasing data quality, improving reporting methods / analysis tools, and developing related policies / processes. Lead and participate in Kaizen and Lean Maintenance events. Lead engineering projects such as equipment or process improvements through project conceptualization, project design, machine design, development of alternatives, project scheduling and control, and project installation and implementation. | 12/31/2020 |
| 9517 | Baxter Bloomington, IN Process Engineer II BS in Engineering Exp: 1-3 Years |
An Engineer II is responsible for continuous improvement, floor support and troubleshooting as required on assigned filling lines and processes (both mechanical and electrical). An Engineer II will be responsible for development of requirements specifications, technical specifications, design specifications, validation protocols, and change control records. This position will work with Program Managers to facilitate new product introduction to the site (vendor relations, procurement, installation, and validation) and achieving both budget and timeline requirements. This position reports to the Manager of Engineering. | 12/31/2020 |
| 9518 | Baxter Bloomington, IN Quality Lab Associate BS in Chemistry or Analytical Chemistry Exp: 0+ Years |
The Quality Lab Associate I (2nd Shift) performs entry-level laboratory testing (pH, density, volume, etc.) that requires a variety of chemical, biological, or physical analyses on products/systems in support of the company’s quality program. This role works as part of the quality unit. This position reports to a Quality Control Chemistry Supervisor. | 12/31/2020 |
| 9519 | Baxter Opelika, AL Quality Lab Technician BS in Chemistry or Biological Sciences Exp: 0-2 Years |
This is a second shift position intended to perform Quality Control Testing to support the acceptance of raw materials and finished products. This position will cross-train to perform all laboratory tests to support dialyzer manufacturing. These tests will include microbiological, chemical, and performance tests. The technician may at the discretion of the QRM Manager have primary responsibility in either the Microbiology Laboratory or the Chemical Laboratory. | 12/31/2020 |
| 9520 | Baxter Cleveland, MS Engineer I BS in Engineering Discipline Exp: 0-1 Year |
Responsibilities: Must perform process validation, process capability, and process control studies for assigned areas. Must drive quality/manufacturing projects utilizing Lean, problem solving, process control, and project management tools to achieve and sustain operational excellence. Must support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new process/technology. Must assist in the identification and development of process improvement projects including automation and computerization. Must ensure computer systems and applications are in compliance with regulatory quality standards through validations activities. Responsible for ensuring FDA regulations are met for system upgrades/replacements. Responsible for ensuring the quality of facility systems (validation). Writing and executing protocols and test cases for validations. Coordinating testing and documentation of projects. | 12/31/2020 |
| 9521 | Be Bio Cambridge, MA Research Associate - Cell Platform MS in Relevant Discipline Exp: 1+ Years |
Responsibilities: Help to establish protocols around differentiation of primary immune cells, including extensive tissue culture work (maintenance, expansion, and banking). Handling and analyzing workflows pertaining to cellular differentiation and profiling with downstream qRT-PCR, protein quantification, and other molecular readouts. Cloning of constructs to support cellular engineering efforts. Detailed record-keeping and protocol refinement as related to molecular and cellular assays. Facilitate efficient transfer of assays to CRO partners where applicable. | 12/31/2020 |
| 9522 | Beckman Coulter Miami, FL Manufacturing Process Engineer BS in Engineering Exp: 0-3 Years |
Responsibilities: Facilitate Kaizen and DIVE teams to ensure accurate use of DBS tools. Identify cost-savings and quality improvement projects in assigned area(s) and move them from concept to implementation. Develops and writes SOP’s to support process changes, implementation of new processes and equipment, ensuring manufacturing documents are crafted, updated, and implemented. Provide mentorship for engineering technicians. Coordinates the launch of new product designs and enhancements to existing product designs to ensure smooth transition to full production. Confers with management, engineering, and other staff regarding manufacturing capabilities, production schedules, and other considerations to ensure smooth transition of new or enhanced product and/or processes to full production. | 12/31/2020 |
| 9523 | Beckman Coulter Brea, CA Proposal Analyst II MS in Relevant Discipline Exp: 0+ Years |
You will be responsible for the development and management of error proof contract documents while maintaining high attention to detail. You will also be required to provide insight and business recommendations based on deal analysis. This role is responsible for identifying any discrepancy or potential gaps in the deal elements and focusing on continuously improving the process; recommending solutions and sharing best practices. Analyst II are responsible for reviewing redlines of contract terms and conditions in close partnership with legal, sales and direct customer interaction for timely turnaround time (TAT). The role will maintain close collaboration with other departments/stakeholders including sales, sales management, operations, marketing, legal and finance. You will need to know how to work independently as well as in a team environment. We are looking forward to partnering with you. | 12/31/2020 |
| 9524 | Beckman Coulter Chaska, MN Supplier Quality Engineer II MS in Relevant Discipline Exp: 0-2 Years |
As the Supplier Quality Engineer II, you will work with cross-functional teams and ensure suppliers deliver quality product on an on-going basis, while developing supplier capabilities for future needs. This includes material specification development, supplier selection & approval, material qualification, material control and supplier development activities. You'll independently plan, coordinate, and report on material projects and supplier performance. Your sound technical ability and decision making will achieve the desired results. You'll represent Supplier Quality on new product development, manufacturing, and product improvement projects. | 12/31/2020 |
| 9525 | Beckman Coulter Carlsbad, CA Senior Technician Quality Control BS in Chemistry, Biology, or Medical Terminology Exp: 1+ Years |
Responsibilities: Testing and inspecting assigned products including raw materials, bulks and final products for clinical chemistry assays, including general chemistry and specialized tests such as therapeutic drug monitoring and drugs of abuse. Weigh samples on analytical balances, prepare solutions, and process samples following defined SOPs. Use general laboratory equipment such as balances, pH meters, and spectrophotometers. Use Beckman Coulter clinical analyzers such as DxC and Immage systems. Investigate and troubleshoot problems when needed. Interface with R&D, manufacturing technical operations, quality assurance, and supply chain within the company. Perform microbiological and spectrophotometric test of clinical diagnostic reagents and finished products. Perform calibration, standardization, and maintenance of laboratory instruments and equipment. | 12/31/2020 |
| 9526 | Beckman Coulter Carlsbad, CA Development Scientist II MS in Biology or Chemical Science Exp: 0-2 Years |
The Research and Development department is looking for a Development Scientist to support the manufacture of clinical chemistry reagents including design changes, failure investigations and Verification/Validation studies. In addition, this role will act as a liaison between Development and current production, facilitating the transfer process and assisting in troubleshooting activities. This individual will also work on future development project initiatives for the department as project priorities and manufacturing support allow. | 12/31/2020 |
| 9527 | Beckman Coulter Minneapolis, MN Mechanical Engineer II MS in Mechanical Engineering Exp: 0-2 Years |
This position will have a focus on investigating, designing and improving mechanical systems including motion control, fluid handling, electro-mechanical system hardware, and packaging. Responsibilities: Lead reliability investigations, cost reduction efforts, and mechanical design improvements. Engage in new product concepting and development. Perform both empirical and theoretical analysis; interpret experimental data to formulate conclusions. Create and maintain detailed component level drawings that include material specifications, material coatings, tolerancing and GD&T. Develop test criteria and executing test plans. Develop project schedules, track and communicate project status, and provide leadership and ownership of project deliverables. | 12/31/2020 |
| 9528 | Beckman Coulter Miami, FL Manufacturing/Process Engineer I BS in Engineering or Related Exp: 0-3 Years |
The Manufacturing Process Engineer for Beckman Coulter Diagnostics takes ownership of determining the optimal manufacturing methods and process. This includes driving continuous improvement to product cost, quality, and performance by using technical experience and judgment to tackle engineering problems. This position is part of the manufacturing engineer team and will be located in Miami, FL. Responsibilities: Facilitate Kaizen and DIVE teams to ensure accurate use of DBS tools. Identify cost-savings and quality improvement projects in assigned area(s) and move them from concept to implementation. Develops and writes SOP’s to support process changes, implementation of new processes and equipment, ensuring manufacturing documents are crafted, updated, and implemented. Provide mentorship for engineering technicians. | 12/31/2020 |
| 9529 | BeiGene San Francisco, CA Document Specialist, Medical Writing BS/MS in Life Sciences Exp: 1+ Years |
The Document Specialist, Medical Writing will support/assist in the writing, editing, formatting and overall development of clinical regulatory documents that conform to domestic and/or international regulatory submission and internal document standards, while meeting project timelines. Clinical regulatory documents include, but are not limited to, study reports, clinical study protocols or amendments, investigator brochures, regulatory briefing documents, and clinical sections of INDs, NDAs, BLAs, MAAs and other regulatory submission documents. | 12/31/2020 |
| 9530 | BeiGene San Mateo/Remote, CA Project Coordinator (Contract) BS in Project Management, Life Sciences or Related Exp: 0-2 Years |
The Project Coordinator will collaborate closely with program managers to provide support for a range of project planning/management activities. This role will work closely with various members of the project team to develop timelines, create schedules, and oversee progress to make sure goals are met on time. Responsibilities: Provide support and assistance to program managers in completion of all required tasks to meet departmental and project goals. Responsible for the maintenance of plans and timelines within MS Project, and communicating project status in designated platforms. Assist with developing program management dashboards, reports and presentations. Generate and publish weekly project and program reports; incorporate process improvements and innovation in developing new reports. Assist in coordinating project/program meetings; collecting agenda and action items and creating meeting minutes. Be an active participant in Project Management staff meetings. | 12/31/2020 |
| 9531 | Berg Framingham, MA Research Associate I - Functional Lipidomics BS/MS in Analytical Chemistry, Biochemistry, or Related Exp: 0+ Years |
The Research Associate I will be responsible for biomarker discovery/validation in multiple disease areas, including neurodegenerative diseases, diabetes, obesity, and cancer, using state-of-the-art quantitative lipidomics platforms. Responsibilities: Familiarity with Mass Spectrometry. Hands-on experience with mass spec quantitative and qualitative data analysis including spectral interpretation is a plus. Excellent communication and interpersonal skills combined with a superior and proven track record of technical and organizational skills. Must be able to work in a team-oriented environment and demonstrate attention to detail and record-keeping. | 12/31/2020 |
| 9532 | Berg Framingham, MA Data Research Associate II - Neurology Scientist BS/MS in Biology, Biochemistry, Neuroscience, or Related Exp: 1-2 Years |
The RA II will characterize novel therapeutic targets for neurodegenerative diseases and assists in the development of potency assays and phenotypic screens in vitro. Responsibilities: Assist in the characterization of novel diagnostic biomarkers and therapeutic targets for Alzheimer’s and Parkinson’s disease using standard molecular biology techniques. Identification, development, and implementation of cutting-edge methods for characterizing lead biomarker and therapeutic candidates. Contribution to assay development and small molecule screens. Maintain and differentiate several cell lines to support the research efforts of the Neurology department. Report research findings in an organized, clear and timely manner. | 12/31/2020 |
| 9533 | Berkeley Lights New York City, NY Applications Development Engineer MS in Chemical, Mechanical, or Electrical Engineering, or Related Exp: 0-3 Years |
This research and development role resides at the interface of several teams within the organization, including the software and hardware engineering teams, the chip design and reagents team, and product marketing. In this position, you will have the opportunity to create new capabilities on the Berkeley Lights platform, taking products from early conception through product launch. Responsibilities: Work closely with collaborators and customers to design solutions leveraging Berkeley Lights’ platforms with a focus on Cell Therapy and T cell immunology applications. Contribute to shaping and guiding the design, development and productization of T cell functional assays uniquely enabled by Berkeley Lights’ platforms. End-to-end workflow development involving precious sample handling, microfluidic-based workflow development, and workflow automation. Validation and verification of complex life science instrumentation. | 12/31/2020 |
| 9534 | Berkeley Lights Emeryville, CA Associate Development Engineer BS/MS in Chemical, Mechanical, or Electrical Engineering, or Related Exp: 0-3 Years |
This research and development role resides at the interface of several teams across Berkeley Lights, including the software and hardware engineering teams, the chip design and reagents team, and product marketing. In this position, you will have the opportunity to create new capabilities on the Berkeley Lights Platform, taking products from early conception through product launch. Responsibilities: End-to-end workflow development involving precious sample handling, microfluidic-based workflow development, and workflow automation. Validation and verification of complex life science instrumentation. Contribution to the invention of core intellectual property (from conception through validation), white papers, and external publications. This research and development role resides at the interface of several teams across Berkeley Lights, including the software and hardware engineering teams, the chip design and reagents team, and product marketing. In this position, you will have the opportunity to create new capabilities on the Berkeley Lights Platform, taking products from early conception through product launch. Responsibilities: End-to-end workflow development involving precious sample handling, microfluidic-based workflow development, and workflow automation. Validation and verification of complex life science instrumentation. Contribution to the invention of core intellectual property (from conception through validation), white papers, and external publications. | 12/31/2020 |
| 9535 | Berkeley Lights Emeryville, CA Development Engineer MS in Chemical, Mechanical, or Electrical Engineering, or Related Exp: 0-3 Years |
This research and development role resides at the interface of several teams within the organization, including the Software and Hardware Engineering teams, the Chip Design and Reagents team, and Product Marketing. In this position, you will have the opportunity to create new capabilities on the Berkeley Lights Platform, taking products from early conception through product launch. Responsibilities: End-to-end workflow development involving precious sample handling, microfluidic-based workflow development, and workflow automation. Validation and verification of complex life science instrumentation. Contribution to the invention of core intellectual property (from conception through validation), white papers, and external publications. | 12/31/2020 |
| 9536 | BioAssay Systems Hayward, CA Research Associate - Assay Development BS in Biochemistry, Chemistry, Biology, or Related Exp: 1-2 Years |
This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers. | 12/31/2020 |
| 9537 | BioAssay Systems Hayward, CA Research Associate - Manufacturing BS in Biochemistry, Chemistry, Biology, or Related Exp: 1-2 Years |
This position will entail preparing reagents for our assay kits, QCing, and packaging the finished products. This candidate may also join part time in our R&D team. | 12/31/2020 |
| 9538 | Bioclinica Newark, CA Clinical Data Manager BS in Computer Science, Life Science, or Related Exp: 1+ Years |
Responsibilities: Understanding the requirements for study implementation and data collection. Collaborating with project team to develop study-specific edit check criteria. Defining, running, and reviewing edit checks and resolving discrepant data. Maintaining organized, complete, and up-to-date study documentation. Performing study setup, including TF design, database structure, specifications, and obtaining and providing approvals as needed. Coordinating and documenting the receipt and processing of electronic or ancillary data received from outside sources (e.g., data received from other central laboratories, CRO's, or Sponsors). Keeping supervisor informed of project status. | 1/3/2021 |
| 9539 | Bioclinica Princeton, NJ Medical Writer BS in Life or Physical Sciences Exp: 1+ Years |
Responsibilities: Performing new award tasks such as entering new studies into the MedComm database, creating Medical Affairs and Medical Communications study-specific folders, organizing study documents, requesting signed Protocols, entering document costs in the new award spreadsheet, and notifying assigned Project Teams. Performing a concise and thorough review of study Protocols related to imaging requirements, schedules and windows. Creating, modifying and finalizing Site Manuals, associated fillable forms, and labels. Creating, modifying and finalizing Study Start-Up related Compliance Reports (CRs) such as Protocol Amendment Impact Forms (PAIFs), Notes to File (NTFs), Corrections, non-Quality Event Deviation Reports, and Transfers of Obligation (ToO) as required/applicable. Creating, modifying and finalizing paper Source Documents/eCRFs for reads performed outside a standard application (e.g., based on ToOs) on an as-needed basis. Creating, reviewing, modifying and finalizing MedComm Meeting Minutes. | 1/3/2021 |
| 9540 | Bioclinica Princeton, NJ Imaging Research Associate BS in Biological or Computer Science Exp: 0+ Years |
Responsibilities: Assist in preparation and reproduction of study materials during study start-up phase of clinical trials. Follow up with outstanding documentations from clinical sites to complete site qualification. Schedule logistical and technical trainings with site personnel. Create test run requests for sites submitting digital data. Review, process, track and monitor all study related data received from sites. Assist in the monitoring and resolution of data discrepancies resulting from discrepancy listings generated from clinical data management. Manage site communications, generate site and patient reports and queries, and verify reports prior to distribution to clinical sites and sponsors. Investigate and complete logistical edit checks. | 1/3/2021 |
| 9541 | Bioclinica Princeton, NJ Clinical Project Manager BS in Life Sciences, Pharmacy, Nursing, or Related Exp: 1-3 Years |
Responsibilities: Reviewing study requirements and response assessment criteria and collaborates with key stakeholders to develop study start-up activities and associated documents. Defining project plans (i.e. timelines, milestones and limitations for project staff). Establishing project reporting schedules. Providing project updates to BD Director, Global Services Managing Directors, Sponsor representative(s) on schedule. Communicating timely, appropriate project information to project teams, sites and company/sponsor representative(s). | 1/3/2021 |
| 9542 | Biodesix De Soto, KS Laboratory Assistant BS in Chemistry, Biology, or Life Science Exp: 0+ Years |
Responsibilities: Pickup, receiving and storage of clinical specimens (i.e., blood); accessioning specimens for clinical testing, making labels, setting up tubes and supplies, logging into the computer-based laboratory information system; inventory management support and general lab assistant type work (e.g., maintaining eye wash station, fire extinguishers, shower, stockroom, etc.). | 1/3/2021 |
| 9543 | Biodesix Boulder, CO Test Processing Specialist I BS in Relevant Discipline Exp: 1-3 Years |
Responsibilities: Data entry of test information. Confirmation of entered data, and confirmation that data provided meets the minimum requirements as indicated by the QMS. Timely and accurate delivery of reviewed test results. Participation in quality and accuracy programs. Other duties as assigned. | 1/3/2021 |
| 9544 | Amunix San Francisco, CA Research Associate, Bioanalytical Sciences MS in Scientific Discipline Exp: 1+ Years |
The successful candidate will be responsible for developing and qualifying Ligand Binding Assays (e.g. ELISA, ECL), quantitative Westerns and/or Cell-Based Assays for pharmacological (PK, PD, and ADA) assessments to help advance research, pre-clinical, and clinical stage programs. The incumbent will analyze pre-clinical study samples using Ligand Binding Assays, cell-based assays, Luminex and/or quantitative Western. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document. | 12/9/2020 |
| 9545 | Analogic Peabody, MA EHS Specialist BS in Environmental, Occupational Health, Safety, Science, or Engineering Related Field Exp: 1-3 Years |
The EHS Specialist will report to the EHS Manager and be responsible for supporting and implementing effective safety and environmental guidelines, policies, and programs that will maintain a safe workplace and meet environmental objectives. The EHS Specialist will assist in maintaining corporate compliance with all appropriate EHS related governmental regulations. At the federal level, this includes OSHA, EPA, RCRA, CERCLA, and SARA. State regulations include Department of Labor and Industries (DLI), the Department of Public Health (DPH), the Department of Environmental Protection (DEP), and Workers Compensation under Department of Labor (DoL). Local community regulations include building and public safety ordinances. | 12/16/2020 |
| 9546 | ANI Pharmaceuticals Baudette, MN Analytical Development Chemist BS in Chemistry, Biochemistry, Microbiology or Related Exp: 1-3 Years |
Responsibilities: Perform testing on raw material, in-process, and finished product samples. Execute compendial method verifications, method transfers and validation in support of new product development. Set-up and confirm suitable operation of equipment and instrumentation. Collect data and generate and report results in accordance with governing test methods and SOPs. Work with management in the vent of discrepancies. Perform review of data collected under approved test methods and investigational plans and protocols, in accordance with governing SOPs. Provide accurate assessment of data integrity, and document findings. Work with management and peers to correct deficiencies. Perform calibrations, preventive maintenance, and repairs as needed on instrumentation. Qualify new equipment as assigned. | 12/16/2020 |
| 9547 | ANI Pharmaceuticals Baudette, MN QC Chemist BS in Chemistry, Biochemistry, Microbiology or Related Exp: 1-3 Years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 12/16/2020 |
| 9548 | ANI Pharmaceuticals Baudette, MN Quality Assurance Specialist I BS in Relevant Discipline Exp: 1 Year |
This position is responsible for providing support to the Manufacturing and Packaging Operations to ensure relevant procedures are followed and meet GMP requirements. Other responsibilities: Perform Packaging Line inspection/audits and provide assurance that packaging operations are compliant with applicable SOPs and GMPs. Perform finished product attribute sample inspection and evaluation of finished products physical characteristics prior to packaging. Perform annual retain sample inspections and control finished product and raw material samples stored in the reserve sample room. Perform Complaint writing. Monitor GMP areas for compliance with general GMP requirements such as proper gowning and cleanliness. | 12/16/2020 |
| 9549 | Applied Medical Rancho Santa Margarita, CA Quality Engineer BS in Engineering or STEM Field Exp: 1-2 Years |
As a Quality Engineer II, you will use your skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. Responsibilities: Conduct experiments to prove hypotheses. Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques. Implement statistical techniques to determine sample sizes and levels of confidence. Implement statistical process controls to monitor validated processes. Design engineering test protocols and use a data-driven approach to collect, analyze and summarize data into engineering reports. Perform root cause investigations for design and manufacturing. Document Non-Conformance Investigations (NCIR). | 12/16/2020 |
| 9550 | Applied Medical Rancho Santa Margarita, CA Electrical Engineer I 4 Year Degree in Computer Engineering, Electrical Engineering, or Related Exp: 0-3 Years |
As a Electrical Engineer you will be responsible for working within the framework of a team and performing the following activities: Schematic design of new and innovative projects. Analyze the hardware and firmware of embedded medical electrical systems with an emphasis on power management, digital and analog controls, and low frequency (500 kHz) high power (500 W) RF amplification. Participate in firmware creation for programmable logic devices such as DSPs, FPGAs, and CPLDs. Participate in hardware and firmware design reviews. Provide design know how for external vendors and supplier development. Support other groups during integration of hardware, firmware, and software. Test and troubleshoot boards and system level electrical systems. Develop, update, and peer-review engineering documents such as instructions, drawings, test procedures and reports. | 12/16/2020 |
| 9551 | Applied Medical Rancho Santa Margarita, CA Process Engineer II BS in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-2 Years |
As a Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. Responsibilities: Develop and sustain manufacturing processes. Debug manufacturing processes and equipment via root cause analysis. Run, observe and expedite shop orders. Develop and update engineering documents such as process maps, process FMEA, Manufacturing / Quality Instructions, Test Methods, drawings, and Test Reports. Collaborate with production to identify capabilities and capacity/ Collaborate with engineering team for fixturing design and development, tolerancing, and design for manufacturing. | 12/16/2020 |
| 9552 | Applied Medical Rancho Santa Margarita, CA R&D Engineer II BS in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-2 Years |
As a R&D Engineer II, you will use skills related to design and development of medical device components and fixtures as part of a cross-functional team. Responsibilities: Create Solidworks models, drawings and assemblies. Build functional prototypes for device development. Perform engineering testing. Debug via root cause analysis. Investigate new tooling, materials, manufacturing processes and technologies. Research and qualify new suppliers and vendors. Complete documentation of design efforts for the Design History File. Develop, update, and peer-review engineering documents such as instructions, drawings, test procedures, and reports. Collaborate with tooling design teams (MIM, Stamping, Molding, etc.). | 12/16/2020 |
| 9553 | Applied Medical Rancho Santa Margarita, CA Complaint Evaluation Engineer BS in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, or Related Exp: 1+ Years |
As a Complaint Evaluation Engineer, you will be responsible for working within the framework of a team and performing the following activities: Evaluate the performance of products returned by the customer. Perform device analysis in accordance with model-specific procedures and protocols. Perform root cause analysis to investigate alleged product deficiencies. Propose corrective/preventive actions as required. Compose detailed reports describing results from investigations. Complete evaluations in a timely and accurate manner. | 12/16/2020 |
| 9554 | Applied Medical Rancho Santa Margarita, CA CNC Machine Operations Engineer BS in Mechanical, Industrial, or Manufacturing Engineering Exp: 1-2 Years |
As a CNC Machine Operations Engineer, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. Responsibilities: Develop and sustain manufacturing processes. Debug manufacturing processes and equipment via root cause analysis. Run, observe and expedite shop orders. Develop and update engineering documents such as process maps, process FMEA, Manufacturing/Quality Instructions, test methods, drawings, and test reports. Collaborate with the Production team to identify capabilities and capacity. Collaborate with the Engineering team for fixturing design and development, tolerancing, and design for manufacturing. Collaborate with tooling design teams (MIM, Stamping, Molding, etc.). Investigate new tooling, materials, manufacturing processes, and technologies. Research and qualify new suppliers and vendors. | 12/16/2020 |
| 9555 | Applied Molecular Transport San Francisco, CA Upstream Manufacturing Associate BS in Chemical Engineering, Microbiology, Biochemistry, or Related Exp: 0-2 Years |
AMT is looking for an Upstream Manufacturing Associate to work in our GMP manufacturing facility to produce biopharmaceutical proteins. The primary focus of the Manufacturing Associate role will be work as part of a team to conduct GMP upstream manufacturing production assignments and tasks with high quality and timely output. Responsibilities: Set-up and operation of single-use fermentation, cell processing, and separation equipment. Process monitoring and sampling, including performing routine sample analysis. Weigh out chemicals, prepare media, solutions, and buffers. Participation in daily operation and routine maintenance of process and analytical equipment. Maintaining a clean and organized lab environment. Chemicals and consumables stocking, etc. Maintaining strict adherence to batch records, SOP’s, and safety guidelines designate for the manufacturing process. | 12/16/2020 |
| 9556 | Applied Molecular Transport San Francisco, CA Scientist/Sr. Scientist BS/MS in Chemistry, Biochemistry, Biological Sciences, Pharmaceutical Sciences, or Related Exp: 1-5 Years |
The Scientist/Sr. Scientist position is within AMT’s analytical development group that is based at Tower Place, South San Francisco. In this role, the scientist will perform method development, qualification, and technology transfer for the release and stability testing of drug substance and drug products. The position will report to Director of Analytical Development and collaborate with cross-functional teams at AMT. Responsibilities: Perform analytical method development for LC based assays such as SEC, IEX and reversed-phase HPLC, and other protein-based analysis (i.e. SDS-PAGE, CE-SDS, A280, etc.). Provide testing support for the in-house manufacture of drug substance and drug product. Execute stability studies to evaluate and characterize protein degradation during storage. Process data and present findings at regular team meetings. Document operating procedures for technology transfer and work to implement methods in a GMP environment. | 12/16/2020 |
| 9557 | Arcus Biosciences Hayward, CA Research Associate/Sr. Research Associate, Immunology BS in Cell Biology, Immunology, or Related Exp: 1-2 Years |
The Biology group is seeking a motivated, energetic, and skilled individual who wishes to play a role in advancing novel immunotherapy drug candidates from the discovery phase into the clinic. The role will be responsible for executing a variety of experiments using in vivo models and in vitro assays in order to validate new targets and understand mechanism of action and pharmacodynamic properties of drug candidates. A successful candidate will contribute as part of a multidisciplinary team in a fast-paced environment to plan and execute experiments and subsequently collate, document, interpret, and present data internally. | 12/16/2020 |
| 9558 | Arcus Biosciences Hayward, CA Sr. Clinical Data Analyst BS/MS in Statistics, Epidemiology, Bioinformatics, or Related Exp: 0-4 Years |
The Sr. Clinical Data Analyst will be responsible for creating fit-for-purpose analyses, visual data displays and dashboards from diverse data types to aid in internal data consumption and decision-making. This position will report into the Head of Statistical Programming and will interact regularly with diverse stakeholders across the organization. Demonstrated abilities to prioritize work; to understand internal business, data and decision-making needs; and to communicate and collaborate with key stakeholders both within Biometrics and beyond (research, translational science, clinical science, clinical operations, safety, medical affairs and commercial) are essential. | 12/16/2020 |
| 9559 | Arcus Biosciences Hayward, CA RA - Lead Discovery and Optimization BS/MS in Biochemistry, Chemical Biology, Molecular Biology, or Related Exp: 0-3 Years |
Arcus is seeking self-motivated, collaborative and highly skilled individuals to work with them to discover novel anti-inflammatory and immunotherapeutic oncology drugs. The opening for an enthusiastic and motivated research associate requires the application of creative problem-solving approaches to the execution of biochemical and cell-based assays to provide insightful SAR (structure activity relationship). The successful candidate will be a rigorous, quantitative, detail-oriented experimentalist coupled with excellent practical laboratory skills and enthusiasm for automated laboratory assay techniques. Responsibilities: Executing micro-plate-based in vitro biochemical and cell-based enzymatic and ligand binding assays. Maintaining mammalian cell culture and conducting transient and stable mammalian cell protein expression. Utilizing liquid handling systems and laboratory robotics to implement in vitro. Performing practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. | 12/16/2020 |
| 9560 | Arcus Biosciences Hayward, CA Research Associate BS/MS in Molecular Biology, Biochemistry, or Related Exp: 0-3 Years |
This position requires the application of creative problem-solving approaches to the execution of new biochemical and cell-based assays. The successful candidate will have excellent practical laboratory skills, coupled with aptitude and enthusiasm for automated laboratory assay techniques. Responsibilities: Performing routine assays to support chemistry efforts. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro. Contribute during lab meetings and assist in the analysis and reporting of experimental data to project teams. | 12/16/2020 |
| 9561 | Arcus Biosciences Hayward, CA Research Associate: Lead Discovery and Optimization BS/MS in Molecular Biology, Biochemistry, or Related Exp: 0-3 Years |
The RA Lead Discovery and Optimization position requires the application of creative problem-solving approaches to the execution of new biochemical and cell-based assays. The successful candidate will have excellent practical laboratory skills, coupled with aptitude and enthusiasm for automated laboratory assay techniques. Responsibilities: Performing routing assays to support chemistry efforts. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro. Contribute during lab meetings and assist in the analysis and reporting of experimental data to project teams. | 12/16/2020 |
| 9562 | Argonaut Manufacturing Services Carlsbad, CA Technical Transfer Operator, Drug Product Manufacturing BS in Life Science or Engineering Discipline Exp: 1-3 Years |
The purpose of this position is to transfer product and process knowledge from developmental clinical production to GMP product manufacturing in the drug product manufacturing division of Argonaut. Responsibilities: Facilitate transfer of new processes from client lab or concept to drug product manufacturing by collaborating with subject matter experts and operations management. Participate in client discussions via phone, video conference, and/or onsite visits. Create and revise client-specific batch records, raw material specifications, and any documentation related to Drug Product Manufacturing. Review executed batch records and other documentation, as needed. Track and trend documentation issues. | 12/16/2020 |
| 9563 | Argon Medical Devices Athens, TX Manufacturing Engineer I BS or Higher in Mechanical or Industrial Engineering Exp: 1-2 Years |
The Manufacturing Engineer will work to gather and document customer requirements, translate them into measurable product requirements, and provide engineering support for the development and manufacture of Argon Medical Device products. The Manufacturing Engineer will recommend, develop, and implement manufacturing-related cost-saving initiatives (Value Improvement Projects) and be responsible for developing and implementing product qualification protocols. The Manufacturing Engineer will confer with vendors to determine product specifications and arrange for purchase of equipment, materials, or parts and evaluate products according to specifications and quality standards, including assisting in the estimation of production times, staffing requirements, and providing related costs information for management decisions. | 12/16/2020 |
| 9564 | ARL Biopharma Oklahoma City, OK Laboratory Technician - Microbiology Lab BS in Microbiology or Related Exp: N/A |
This job operates in a laboratory environment. Attendance at the office is required. While performing the duties of the job the employee is frequently exposed to various microorganisms and may be exposed to toxic or hazardous chemicals. The employee will be required to wear all appropriate safety equipment including but not limited to eye protection, gloves, full face respirator and lab coat. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Responsibilities: Media preparation, glassware cleaning, inventory / ordering, lab cleaning and sanitization, and autoclaving various reagents and supplies. Assist laboratory personnel in daily activities to maintain high scientific quality and compliance with SOPs, protocols, and safety standards. | 12/16/2020 |
| 9565 | ARL Biopharma Oklahoma City, OK Laboratory Technician - R&D Lab BS in Chemistry or Related Exp: N/A |
R&D Lab Tech performs general laboratory tasks under immediate supervision. The work involves preparation of chemical reagents/mobile phase, assistance with chemical tracking/disposal, and assistance with sample retrieval, preparation and storage. The position requires ability to use a personal computer, including familiarity with word processing, spreadsheet, email and database applications. Responsibilities: Prepare chemical reagents/mobile phase. Assists chemical tracking/disposal. Assists sample retrieval, preparation and storage. Order and organize general lab supply. Wash glassware and maintain lab cleanness. | 12/16/2020 |
| 9566 | ARL Biopharma Oklahoma City, OK Laboratory Technician - Analytical Lab BS in Chemistry or Related Exp: N/A |
Responsibilities: Adhere to Quality Management System (QMS). Follow prescribed safety rules and regulations in performing all assigned duties. Follow written and oral instruction. Prepare reagents, solutions, and mobile phases required for testing. Perform timely peer review of laboratory notebooks. Sample management including retrieval, storage, and disposal. Work and think independently, yet share ideas and work towards team goals. Use a personal computer including word processing, spreadsheets, email and database applications. Express thoughts in a clear concise manner both orally and written. Work to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities. Ability to wear, maintain, and properly use appropriate safety equipment, including, but not limited to eye protection, gloves, and lab coat. Adherence to all ARL Bio Pharma safety standards, policies, procedures, and protocols. | 12/16/2020 |
| 9567 | Arraystar Inc Rockville, MD Lab Assistant - Molecular Biology BS in Relevant Biological Field Exp: 1-2 Years |
Responsibilities: Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 12/16/2020 |
| 9568 | Arthrex Naples, FL Associate Product Manager - Imaging BS/MS in Relevant Discipline Exp: 1 Year/0 Years |
The Associate Manager plans, organizes, and controls an assigned product line from conceptual stages through product life cycles to optimize profit and meet marketing, financial, and corporate growth objectives by performing the following duties. Responsibilities: Participates in overall marketing, product strategy, research and development requirements, development, and manufacturing coordination for new and emerging products. Works on technical product development, estimates of potential profits, and release to production. Assists in the management of day-to-day progress and maintenance of products. Provides technical expertise and training to other departments in support of product development. Works with Product Team to develop marketing analysis to determine product definitions. | 12/16/2020 |
| 9569 | Arthrex Naples, FL Associate Product Manager - Fluid Management BS/MS in Relevant Discipline Exp: 1 Year/0 Years |
Responsibilities: Participates in overall marketing, product strategy, research and development requirements, development, and manufacturing coordination for new and emerging products. Works on technical product development, estimates of potential profits, and release to production. Assists in the management of day-to-day progress and maintenance of products. Provides technical expertise and training to other departments in support of product development. Collaborates with a wide variety of functional areas such as sales, engineering, marketing, manufacturing, and operations to develop and provide product definitions responsive to customer needs and market opportunities. Provides financial and technical justification for product selection and definition. Conducts market research and identifies and tracks market trends in company's industry. Produces competitive analysis materials comparing product with its key competitors. Participates in key sales situations for the product. Works with PM to define promotional activities, publicizing the product through the press, sales force, and alternate distribution channels. | 12/16/2020 |
| 9570 | MeiraGTx New York City, NY Research Associate, Molecular and Protein Engineering BS in Life Science Discipline Exp: 0-2 Years |
MeiraGTx is seeking a motivated, enthusiastic, well-rounded individual with experience in molecular biology and biochemistry to be a part of an early pre-clinical stage Molecular and Protein Engineering group to develop better, smarter gene therapies. For this position, under the guidance of senior scientists, the successful candidate will be primarily responsible for the general laboratory upkeep of the research group and assisting in the construction of mammalian plasmids harboring engineered transgene cassettes, performing transient expressions of said plasmids in relevant mammalian cell lines, and subsequent testing of the expressed transgenes for improved functions using in vitro biochemical and/or cell-based assays. | 12/16/2020 |
| 9571 | MeiraGTx New York City, NY Technician, Molecular and Protein Engineering BS in Life Science Discipline Exp: 0-2 Years |
MeiraGTx is seeking a motivated, enthusiastic, well-rounded individual with experience in molecular biology and biochemistry to be a part of an early pre-clinical stage Molecular and Protein Engineering group to develop better, smarter gene therapies. For this position, under the guidance of senior scientists, the successful candidate will be primarily responsible for assisting in the construction of mammalian plasmids harboring engineered transgene cassettes, performing transient expressions of said plasmids in relevant mammalian cell lines, and subsequent testing of the expressed transgenes for improved functions using in vitro biochemical and/or cell-based assays. | 12/16/2020 |
| 9572 | MeiraGTx New York City, NY Technician, Molecular and Protein Engineering BS in Molecular Biology, Cellular Biology, or Related Exp: N/A |
MeiraGTx is seeking motivated and enthusiastic technicians to join their growing research and development team. The applicant should have experience using standard molecular and cellular biology techniques, will be required to present results and updates at project team meetings, maintain accurate and well-organized experiment records. The qualified candidate will work independently and as part of a team to closely collaborate with other team members. Responsibilities: Maintain cultures of mammalian cell lines. Plasmid DNA extraction and purification, quantification. Perform cell-based assays, high throughput screening. Analyze, interpret and present experimental results accurately, maintain clear and up-to-date experiment records. | 12/16/2020 |
| 9573 | Aruna Bio Athens, GA Biomanufacturing Associate BS in Biological Science, Cell Biology, Biomedical Engineering, or Related Exp: 0-2 Years |
The Biomanufacturing Associate supports the the manufacturing efforts of ArunA Bio, and must work collegially and collaboratively as part of a larger team. The position requires the individual to carry out complex stem cell manufacturing with an advanced degree of detail, and in accordance with established SOPs, cGMPs, and safety regulations. The individual will work as a member of a team responsible for performing all bioprocessing workflows. | 12/16/2020 |
| 9574 | Atara Bio Thousand Oaks, CA Manufacturing Associate BS in Scientific Discipline Exp: 0-2 Years |
The Manufacturing Associate works as part of the manufacturing team to deliver high quality cell therapy materials during process transfers, routine production, and technology improvements. This position contributes to the successful delivery of released product in support of clinical trials and commercial production. Responsibilities: Support production in an aseptic environment. Executes on production batch records and work orders according to SOPs. Assist in all areas of cell culture and all related duties as required including (stocking, tracking inventory, material movement, maintaining metrics, filling out log sheets, and other special projects). Assists in manufacturing batch record review. Routine maintenance and cleaning of rooms and equipment. Identifies and implements continuous improvements. Perform tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. Adhere to all safety protocols and procedures. | 12/16/2020 |
| 9575 | Atara Bio Thousand Oaks, CA Research Associate - CAR-T Development BS in Cell Biology, Immunology, Molecular Biology or Related Exp: 1+ Years |
The Research Associate - CAR-T Development is an integral member of the Preclinical Immunotherapy Research group. This role will be responsible for the generation and characterization of novel CTL and Chimeric Antigen Receptor (CAR) T cell therapies. The successful candidate will perform experiments to support new product development and IND-enabling activities for Atara’s CAR T cell pipeline. Other responsibilities: Performs retroviral (gamma retrovirus and/or lentiviral) transductions of primary T cells and propagation. Evaluates allogeneic CAR T cell activity, efficacy, and alloreactivity. Performs primary immune cell isolation and multi-parameter immunophenotyping by flow cytometry. Designs and executes assays to evaluate target-specific T cell characteristics and function. | 12/16/2020 |
| 9576 | Atara Bio Thousand Oaks, CA Research Associate Viral Vector Process Development BS in Relevant Discipline Exp: 1+ Years |
The Viral Vector Process Development Research Associate is an active member of a growing viral vector process development team supporting Atara’s T-cell therapy programs. The individual will contribute to the development, scale up and technology transfer of the viral vector production with focus on cell culture development and scale-up. These activities can include aseptic cell culture of viral vector suspension and/or adherent cell lines, scale-down model and qualification, scale-up development, process optimization, robustness studies, and process characterization. Experience with both suspension and adherent formats are desired. This position includes viral seed stock production, viral vector production and purification, virus process development and scale-up, and analytical testing of in-process controls. | 12/16/2020 |
| 9577 | Atara Bio Thousand Oaks, CA Associate Scientist - Analytical Development MS in Biological Sciences Exp: 1-5 Years |
The Associate Scientist will work with the Analytical Development team to develop and execute analytical methods to characterize T cell therapy manufacturing processes and products across the Atara EBV T-cell platform, with an emphasis on flow cytometric methods for characterization and lot release. The candidate will design and execute experiments, organize, document, analyze and interpret results using sound scientific principles. The candidate will present data to cross-functional teams, and thus strong written and verbal communication is essential. | 12/16/2020 |
| 9578 | Athenex Clarence, NY Quality Control Laboratory Technician BS in Chemistry or Related Exp: 6+ Months |
The technician will support the laboratory workflow in an efficient and effective manner and support the analytical group in maintaining the laboratory to make workflow more efficient. Responsibilities: Promoting and maintaining safe and healthy working conditions in his I her assigned work area; instructs and enforces compliance with established safe work practices and procedures. Properly disposes of solvent waste in appropriate containers and disposes of empty bottles in the recycling bins according to health, safety and environmental practices. Performs laboratory, office and maintenance on a routine basis. Performs and documents periodic checks of the eye wash stations located in the laboratory. | 12/16/2020 |
| 9579 | Atreca San Francisco, CA Research Associate I/II, in vitro Pharmacology BS in Cell Biology, Immunology, or Related Exp: 1+ Years |
Atreca is seeking a Research Associate (RA) who will apply her/his skills in cell biology and flow cytometry to screen the growing library of Atreca antibodies for binding against tumor cells. The successful candidate will work in a fast-paced and team-based environment with opportunities to collaborate across different functional groups within the organization. Responsibilities: Harvest and stain cells for screening using flow cytometry in a high throughput format. Flow data analysis and quality control and assay optimization. Follow laboratory safety guidelines and practices. | 12/16/2020 |
| 9580 | Atreca San Francisco, CA Research Associate - Molecular Biology BS/MS in Molecular Biology or Related Exp: 0-3 Years |
Atreca is seeking a highly skilled candidate to apply her/his skills to discover novel anti-cancer biologics by leveraging the cancer patient immune response. This will include using molecular biology skills to build and sequence patient antibody repertoires and perform interrogations using antibody display and selection techniques. The successful candidate will become a key member of the R&D team, deeply involved in experimental planning, troubleshooting, and execution. She/he will perform experiments, analyze data, and present her/his research findings to interdisciplinary teams. Strong analytical skills, excellent written and verbal communication skills, and attention to details are extremely important for this position. | 12/16/2020 |
| 9581 | Atreca San Francisco, CA Senior Research Associate, Protein Engineering MS in Cell Biology, Immunology, Bioengineering or Related Exp: N/A |
The successful candidate will play a key role producing and characterizing antibodies and engineered bispecifics in support of pre-clinical studies. This position will have the opportunity to interact and collaborate with a multidisciplinary team and utilize a variety of biophysical techniques to characterize novel therapeutics. Responsibilities: Scout small-scale productions and develop new purification methods to support scale ups of novel therapeutics (antibodies and bispecifics). Produce and purify novel therapeutics at multi-Liter scale for use in pre-clinical studies. Develop and perform analytical methods, including SEC, IEX, HIC, MALS, BLI, SPR, Tm/Tagg and SLS/DLS. | 12/16/2020 |
| 9582 | AtriCure Mason, OH Regulatory Affairs Specialist BS in Relevant Discipline Exp: N/A |
This position will originate appropriate documents to obtain and maintain marketing privileges consistent with applicable government requirements where AtriCure conducts business. This position will also maintain internal documentation of such approvals and handle requests for documentation from our international distributors and customers. This position is responsible for practicing Quality System Manual procedures and complying with its requirements, and carrying out responsibilities as outlined in safety, health and environmental policies. | 12/16/2020 |
| 9583 | ATUM Newark, CA Cell-Line Development Associate BS/MS in Biology, Molecular Biology, Cell Biology, Biochemistry, or Related Exp: 1+ Years |
ATUM is in need of an experienced Cell-Line Development Technician to join their team and help lead the development of their growing Cell Line Development Division. You’ll be a key part of the production process and have the opportunity to work with multiple departments in a fun and collaborative work environment. The successful candidate should possess: Excellent hands-on tissue culture experience with HEK and CHO cell-lines. A proven track record in an industrial setting in the development of enhanced mammalian expression platforms through host cell line engineering strategies. Successful experience generating stable cell lines for protein expression. The ability to work collaboratively within and across departments. | 12/16/2020 |
| 9584 | ADMA Biologics Boca Raton, FL QA Specialist II - Quality, Engineering, Validation BS in Relevant Discipline Exp: 1-5 Years |
The QA Specialist II-Quality, Engineering, Validation will Perform a wide variety of Quality Assurance activities to ensure compliance with related regulatory requirements. Primarily responsible for the efficacy and compliance of the change control management system, validation and qualification systems, Corrective and Preventive Action reports (CAPA) and Risk Management policies and procedures. Other responsibilities: Ensure cGMP and regulatory compliance as defined in government regulations such as 21 CFR Parts 11, 210, 211, and 600, as well as compliance with corporate policies and procedures. Perform QA review and approval of Change Control and Corrective Action Preventive Action (CAPA) Quality Systems. Independently assess required supporting documentation to support change and corrective/preventive actions. Assist in the Change Review Board (CRB) to ensure that changes are initiated, evaluated, properly classified, authorized and implemented in accordance with Regulatory and Corporate requirements. | 12/2/2020 |
| 9585 | ADMA Biologics Boca Raton, FL Technician I, Manufacturing Purification BS in Chemistry or Life Science Exp: N/A |
This position is under direct supervision of the Group Leader. It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. | 12/2/2020 |
| 9586 | Admera Health South Plainfield, NJ Associate Scientist I, Project Management BS/MS in Biological Sciences Exp: 1+ Years |
Responsibilities: Relay standard information on next generation sequencing applications to customers. Standard communication with prospective, current, and past customers. Co-coordinating multiple genomic projects with excellent documentation skills and communication to customers. Materials purchasing support for laboratory team. Collaborate within group to streamline incoming, ongoing, completed projects – minimally cross-departmental. Learn relevant next generation sequencing materials for RUO applications. Comply with all CLIA/CAP regulations. | 12/9/2020 |
| 9587 | Admera Health South Plainfield, NJ Associate Scientist I/II - Lab BS/MS in Biological Sciences Exp: 1+ Years |
Responsibilities: Preparing solutions and reagents for performing assays on the bench. Perform Next Generation Sequencing-based genomic assays on different workflows: RNAseq, Whole Genome Sequencing, Whole Exome Sequencing. Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. Strict record keeping of all laboratory procedures. Collaborate within the group and cross departmental to achieve goals. | 12/9/2020 |
| 9588 | Akadeum Life Sciences Ann Arbor, MI Research and Development Scientist MS in Relevant Biological or Chemical Science Exp: 1 Year |
The ideal candidate will be comfortable working in a fast-paced, early stage company environment and will be flexible to accommodate shifting company priorities. The individual will independently design, execute, and analyze experiments to advance goals relative to specific projects as well as contribute to a variety of R&D responsibilities including routine lab maintenance, assay development and validation, quality control, and cross-departmental support. The ideal candidate is highly motivated and is willing to adapt to shifting priorities and switch between projects seamlessly. This position will fulfill a variety of roles instrumental to the successful development of Akadeum’s growing platform capabilities. | 12/9/2020 |
| 9589 | Akoya Biosciences Marlborough, MA Associate Research Scientist MS in Cell Biology Exp: N/A |
As an Associate Reagent Scientist, you will work in a dynamic, team-oriented environment and take part in developing multiplex fluorescent immunohistochemistry (IHC) Reagents products for use in cutting-edge research. This position also includes working for the Quality team to provide technical support for new and on-market products QC. The desired skillset for laboratory work includes the ability to perform immunohistochemistry (IHC) procedures and analytical analysis for product development and product support. Your work will mainly involve manual laboratory work and the use of automated stainer systems for monoplex and multiplex fluorescence tissue staining. | 12/9/2020 |
| 9590 | Alcami Wilmington, NC Assistant Scientist II BS in Pharmaceutical Sciences, Chemistry, or Equivalent Exp: 1-2 Years |
The Assistant Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Analytical Assistant Scientist II may also assist with method development/method validation projects. Typical types of testing: assays (potencies, related substances, residual solvents, metals etc.), rate of release (dissolution), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 12/9/2020 |
| 9591 | Alcami Durham, NC Assistant Scientist II BS in Pharmaceutical Sciences, Chemistry, or Equivalent Exp: 1-2 Years |
The Assistant Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Analytical Assistant Scientist II may also assist with method development/method validation projects. Typical types of testing: assays (potencies, related substances, residual solvents, metals etc.), rate of release (dissolution), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 12/9/2020 |
| 9592 | Alcami Wilmington, NC Associate Scientist MS In Pharmaceutical Sciences, Chemistry, or Equivalent Exp: N/A |
The Associate Scientist may be required to work on method development/method validation projects. For this position HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 12/9/2020 |
| 9593 | Alcami St. Louis, MO Chemistry Quality Specialist II MS in Chemistry, Biology, or Related Exp: 1+ Years |
The Chemistry Quality Specialist II is accountable for activities which may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 12/9/2020 |
| 9594 | Aldevron Fargo, ND Associate Process Validation Specialist BS in Biology, Biochemistry, Engineering, or Related Exp: N/A |
The Associate Process Validation Scientist supports internal and external Process Validation and Robustness activities with projects focused on understanding and reducing process variability to improve product quality, cost, and process efficiency. This position also supports Cleaning Validation and Facility Environmental Monitoring Qualifications to ensure the production environment is compliant with regulatory requirements. Other responsibilities: Work collaboratively to design, conduct, and report findings on experiments characterizing new or changed manufacturing processes and new equipment or technology. Support continuous improvement projects addressing process variability, efficiency, product cost and data analysis. Compile, maintain and analyze critical data supporting R&D, engineering and validation work. Execute and/or coordinate execution of process, cleaning, shipping and continued process verification activities. | 12/9/2020 |
| 9595 | Aldevron Fargo, ND Lab Technician III - GMP BS Preferred Exp: 1+ Years |
The Lab Technician will work daily within Aldevron’s labs performing tasks associated with Aldevron’s GMP-Source services. The Lab Technician is expected to become familiar with all Aldevron’s products and to be able to perform most tasks associated with the purification of plasmid DNA. Other responsibilities: Detailed, thorough cleaning, line clearance, and segregation of GMP-Source production areas and associated equipment while wearing appropriate gowning. Training of Lab Technician II personnel. Assist in completing component list compilation as needed. Initiation and completion of deviation forms and Corrective Action documents. Organization and planning of buffer preparation area. | 12/9/2020 |
| 9596 | Aldevron Madison, WI Metrology Technician BS in Metrology or Medical Equipment Technology Preferred Exp: 1-3 Years |
The Metrology Technician will ensure that all equipment is installed, qualified, maintained and calibrated properly, on schedule and complying with any industry or site standards. This position is responsible for performing a wide variety of activities following site operational and safety procedures in a laboratory and manufacturing setting. Work will include mechanical service calls, inspections and in-house repairs and preventive maintenance throughout the facility. Other responsibilities: Perform a variety of installation, maintenance, troubleshooting and repair duties on the facility and lab equipment, as assigned. Perform routine calibration, preventive and scheduled maintenance to ensure compliance of the equipment/system for its intended use is maintained and that manufacturing operational requirements are met. Schedule outside venders to preform maintenance and calibration and ensure that tasks are completed on time. | 12/9/2020 |
| 9597 | Aldevron Fargo, ND mRNA Biomanufacturing Operator BS in Life Sciences Exp: 6+ Months |
The mRNA Biomanufacturing Operator II will work daily within Aldevron’s manufacturing labs performing tasks associated with the production of mRNA. Initially this individual will perform manufacturing for research grade and GMP while learning the production of mRNA. This planning for production activities, performing upstream and/or downstream tasks, and documenting production activities. This role reports into R&D. Other responsibilities: Perform various manufacturing tasks in accordance with Aldevron Standard Operating Procedures. Review daily work instructions and organize individual daily workflows. Document manufacturing activities on the Aldevron Internal Database. Complete work independently under daily written direction from the Production Supervisor(s). | 12/9/2020 |
| 9598 | Alira Health Framingham, MA Business Development Associate, Clinical BS/BA in Business or Science Exp: 1-2 Years |
The Associate, Clinical Development is an important member of the Alira Health Clinical team. The Associate will be responsible for facilitation and tracking of all client outreach and will attend client meetings (both in person and remotely). The Associate works closely with the Manager of Clinical Development and will provide administrative support in identifying target clients, potential markets, and tracking related information. As a junior member of the Clinical Development team, the Associate will take on additional tasks as needed, including creation of client-facing materials and presentations and may attend industry conferences as needed. This position includes some travel. Other responsibilities: Assist with the development new business for Alira Health’s regulatory, clinical, and market access practices. Demonstrate an understanding of Alira Health’s range of services, with a focus on regulatory clinical trial, and market access services. Schedule and participate in new client teleconferences and meetings, acting as a facilitator for the senior Clinical Development team members. Track current and past clients, including follow-up, deadlines, and metrics, utilizing Salesforce and other tools. | 12/9/2020 |
| 9599 | Alira Health Framingham, MA In-House Clinical Research Associate BS/BA in Relevant Discipline Exp: 1-2 Years |
The In-house Clinical Research Associate (In-house CRA) is an important member of the Alira Health Clinical team. In-house CRAs manage and support clinical sites from site approval through close-out. In-house CRAs work closely with field CRAs and Project Managers without the need for frequent travel. Other responsibilities: Develops study documents and tools, including Informed Consent Form (ICF) templates (for both local and central IRBs), site binder contents, tip cards, etc. Supports sites in obtaining IRB approval, developing submission materials, and creating site-specific ICFs. Responds to sites’ regulatory board requests for protocol and ICF clarification as needed. Ensures all required site regulatory documents and approvals are in place prior to investigational product shipment. | 12/9/2020 |
| 9600 | Allogene Therapeutics San Francisco, CA Associate Scientist, Process Development BS/MS in Chemical Engineering, Biochemistry, Molecular Biology, Cell Biology, Immunology, or Related Exp: 1+ Years |
Allogene is current seeking a highly motivated Associate Scientist to join an exciting team in the allogeneic cell therapy industry. This is a 6+ month contract opportunity in the Process and Product Development group. Responsibilities: Support formulation & drug product development activities for allogeneic CAR T cell therapy products. Actively contribute to drug product process development and characterization. | 12/9/2020 |
| 9601 | Almac Durham, NC Project Coordinator, Distribution BS in Business or Science Exp: 6+ Months |
The Project Coordinator - Distribution supports the Project Manager - Distribution by providing a back-up resource, in addition to managing some accounts themselves. The main objective of the position is to interpret customer supplied information and transform it into instructional documentation for operational distribution staff to complete shipments. The principal function of the project services department is the day-to-day management of all customers across any Almac Clinical Services (ACS) site. Responsibilities: In charge of interpreting customer supplied information, defining requirements, and generating associated documentation to support operational distribution staff in the shipment of finished goods, components, and ancillary items. The Project Coordinator - Distribution will assist the Project Manager - Distribution with all tasks associated with the successful management of the distribution and return of clinical trial supplies. Generate instructions for return, accountability and destruction at Almac facilities and Almac contracted depots. | 12/9/2020 |
| 9602 | Almac Audubon, PA QC Inspector BS in Scientific Discipline Exp: 1+ Years |
The Quality Control Inspector will provide support to the QC analysts and ensure that all QC tasks are completed on time and are within Good Laboratory Practice. They will also carry out sampling and testing of packaging materials and sampling of starting materials and products and complete the required documentation according to specified standard operating procedures. Responsibilities: Sample starting materials and pharmaceutical products in line with approved SOPs. Perform finished goods inspections and conduct physical tests. Review results of testing carried out by other QC Inspectors. | 12/9/2020 |
| 9603 | Almac Souderton, PA QC Inspector Grade 1, Incoming Goods BS in Scientific Discipline Exp: 1+ Years |
The QC Inspector Grade 1 – Incoming Goods will Sample, inspect and release incoming goods ensuring compliance with approved material specifications, cGMPs, SOPs, and other written quality standards. Responsibilities: Perform incoming goods sampling, inspection, and approvals in compliance with approved material specification, cGMP and Almac Clinical Services SOPs. Complete calibration checks on balances and scales. Sample clinical materials upon customer request. | 12/9/2020 |
| 9604 | Alstem Cell Advancements Richmond, CA Research Associate BS/MS in Biochemistry, Molecular Biology, or Related Exp: 1+ Years |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 12/9/2020 |
| 9605 | Amarex Germantown, MD Clinical Data Coordinator BS in Relevant Discipline Exp: 1+ Years |
Responsibilities: Review and validate clinical trial data. Review case report forms and clinical data sets for errors, discrepancies and protocol violations. Ensure timely completeness and accuracy of databases. Adhere to company procedures related to data handling & data base validation. Implement data entry conventions. Organize and maintain clinical study databases to support regulatory submissions. Design case report forms and related data entry applications. Maintain a thorough understanding of regulatory requirements for data processing operations. Organize and track CRFs, project documents, supplies and enrollments. Participate in project team meetings and recommend processes that lead to timely and successful completion of administrative tasks. | 12/9/2020 |
| 9606 | Amarex Germantown, MD Data Administrator I BS in Statistics, Mathmatics, Physical Science, or Equivalent Exp: 0+ Years |
The Data Administrator I is responsible for maintaining and coordinating the production of datasets and acting as a point of contact for questions regarding the data. Other responsibilities: Prepare mapping specifications for interim datasets. Convert interim data to CDISC (SDTM & ADaM). Prepare Tables/Listing Templates for programming. Assists in the quality check of data listings/tables prior to transmission to other groups or inclusion in interim/final reports. Adhere to company procedures related to data handling & data base validation. Maintain a thorough understanding of regulatory requirements for data processing operations. Participate in project team meetings and recommend processes that lead to timely and successful completion of administrative tasks. | 12/9/2020 |
| 9607 | Amarex Germantown, MD Proposal Development Associate BS in Scientific or Business Related Field Exp: 0+ Years |
The Proposal Development Associate works as part of the Business Development team by providing support in the development of project proposals, work orders, amendments, and vendor contracts, including budgets for all the preceding. The Associate may participate in sales presentations, client interactions, marketing efforts, and other business development functions. Responsibilities: Support the development of proposals, work orders, and amendments for projects in consultation with Business Development team. Support project budget preparation in consultation with supervisor. Negotiate contracts and budgets with sub-vendors as necessary. Support handoff of new projects to operating team. Maintain client and company experience databases. Provide support to sales and marketing groups as needed. Provide miscellaneous support to the Business Development team as needed. | 12/9/2020 |
| 9608 | Amarex Germantown, MD Quality Assurance Assistant BS in Biotechnology Field Exp: 1+ Years |
The Quality Assurance (QA) Assistant provides support to the Quality Assurance department. Responsibilities: Tracking QA project timelines. Assisting with scheduling of internal and external meetings and audits. Preparing and distributing audit/meeting agendas and minutes. Maintenance of employee training files. Maintaining QA department files. Attending training sessions for all departments. Other general administrative support duties as assigned. | 12/9/2020 |
| 9609 | Amarex Germantown, MD Safety Coordinator BS in Scientific or Health Related Field Exp: 0+ Years |
The Safety Coordinator will assist in data entry of adverse events, reviewing the data and communications such as query generations in Clinical Trials. Responsibilities: Enter incoming data into related tracking systems and databases. Handle incoming data from clinical trial sites. Follow the company and department SOPs and other regulatory guidelines, if required. Write data summary narratives and reports, as needed. Perform data reconciliation for ad hoc and annual reports. Organize, attend and take minutes of meetings. Provide administrative/logistical support. Other duties, as assigned e.g. assist with coding activities. | 12/9/2020 |
| 9610 | Amarex Germantown, MD Safety Data Analyst Graduate Degree in Medical Sciences Exp: 0+ Years |
The Safety Data Analyst processes Adverse Event (AE) and Serious Adverse Event (SAE) cases promptly and with medical accuracy. The Safety Data Analyst will also assist the Supervisor with Medical Coding and Medical Monitoring activities and overseeing the overall conduct of pre- and post-marketing studies with regard to Safety of the subjects. Responsibilities: Develop Clinical Safety, Medical Coding and Medical Monitoring plans. Code medical data including medications (utilizing WhoDrug), adverse events and serious adverse events (utilizing MedDRA). Process, document, and report information on Adverse and Serious Adverse Events to the client and the FDA. Prepare safety narratives. Prepare safety case reports to the FDA and regional regulatory agencies using MedWatch and CIOMS-I forms, and annual/periodic safety reports. | 12/9/2020 |
| 9611 | AmbioPharm Augusta, SC Quality Assurance Trainer BS in Biology, Chemistry, or Other Life Science Exp: 1+ Years |
Responsibilities: Provide training to new employees on cGMP concepts, SOPs, Batch Record execution, Batch record reviews, and Investigations. Basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Review proposed SOP revisions and provide feedback to management. Real-time audit of batch records in the production suites for completeness, documentation, calculation errors and conformance to critical process parameters. Perform room and equipment clearances per procedure following cleaning conducted by production. Data entry to support water, HVAC, and other utilities. Complete additional tasks as assigned by the supervisor. | 12/9/2020 |
| 9612 | AmbioPharm Augusta, SC Quality Control Chemist I BS in Chemistry or Life Science Exp: 1-2 Years |
Responsibilities: Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Perform and review QC release testing. Support routine analytical testing using GC, KF, and HPLC. Assist the QC/QA group with writing and editing of SOPs and STPs. Support analytical method development. Perform method transfer and validation activities. Perform OQ/PQ for the Quality Control Equipment. Other duties as assigned. | 12/9/2020 |
| 9613 | Ambry Genetics Aliso Viejo, CA CLS Extraction and Distribution BS in Chemical, Physical, Biological, or Clinical Laboratory Science Exp: 0-4 Years |
The Clinical Laboratory Scientist (CLS) is responsible for following all standard operating procedures of the laboratory and adhering to all quality regulations. Additionally, the technologist may be assigned duties by the Lab Manager, Lab Supervisor, and other Clinical Laboratory Operations Leadership for the advancement or maintenance of the laboratory. Other responsibilities: Follow all procedures and protocols pertaining to patient sample processing, pre-analytical, analytical, and post-analytical testing and general laboratory system that do not directly involve the manipulation of patient samples or products generated from patient samples of assigned assays (typically 1-2 methodologies). Adhere to all Quality regulations (CAP, CLIA & New York State) and ensure all training and competency forms are complete. Daily processing of patient samples within assigned workflow or assay. This includes generating work lists, plate maps, pulling and filing of primers and reagents daily, pulling and filing of patient samples daily and accurately processing of samples within assigned workflow or assay within specified TAT’s. Timely and accurate completion and update of sample processing paperwork and lists on a daily basis either manually or electronically making sure to note any abnormal issues. | 12/9/2020 |
| 9614 | Ambry Genetics Aliso Viejo, CA CLS I - Clinical Validations BS in Chemical, Physical, Biological, or Clinical Laboratory Science Exp: 0-2 Years |
The Clinical Laboratory Scientist I (CLS I) is responsible for following all standard operating procedures of the laboratory and adhering to all quality regulations while leading the validation of new assays and process improvements to the clinical laboratory of one to two assigned methodology workflows. Additionally, the technologist may be assigned duties by the Clinical Validations Director Manager, Clinical Validations Supervisor, and Clinical Validations Lead. Other responsibilities: The CLS I, Clinical Validations may be assigned to a specific methodology workflow or no more than two workflows. Validate an existing or newly developed assay or technology per CAP, CLIA and New York (NY) guidelines. Evaluate new in-house and third-party software systems and validate the software. Ensure validation plans and summaries are written per CAP, CLIA and NY requirements alongside developing and /or updating the SOPs appropriately. | 12/9/2020 |
| 9615 | Amicus Therapeutics Philadelphia, PA Associate Scientist, Bioanalytical Group MS in Chemistry, Biology, or Related Exp: 0-2 Years |
Amicus is seeking an Associate Scientist to join the Bioanalytical team and perform LC-MS/MS method development and study sample analysis to advance Amicus projects and programs. Responsibilities: Performing routine analysis for the quantification of small-molecule drugs, lipids, biomarkers and peptides in biological samples using defined LC-MS/MS methods. Processing and evaluating analytical data obtained from LC-MS/MS analysis of study samples using appropriate software. Reporting results of the study sample analysis, prepare study associated documentation, and maintain an electronic laboratory notebook. Developing novel LC-MS/MS methods for the quantification and/or characterization of proteins and biomarkers of disease. | 12/9/2020 |
| 9616 | Amneal Pharmaceuticals Brookhaven, NY Scientist I, Quality Control BS in Chemistry or Related Exp: 1+ Years |
The Scientist I - QC is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. Other responsibilities: Performs physical and chemical analysis of raw materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques adhering to company policies as identified in standard operating procedures (SOPs). Prepares samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and other analytical techniques as applicable. | 12/9/2020 |
| 9617 | Amneal Pharmaceuticals Brookhaven, NY Scientist II, Quality Control MS in Chemistry or Related Exp: 1+ Years |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. Other responsibilities: Performs chemical analysis of raw materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques, adhering to company policies as identified in standard operating procedures (SOPs). | 12/9/2020 |
| 9618 | Amneal Pharmaceuticals Brookhaven, NY Production Engineer BS/MS in Engineering Discipline Exp: 0-1 Years |
The Production Engineer plans and designs methods to improve production processes. Reviews existing processes and develops solutions to increase productivity or reduce costs. Ensures compliance with approved production methods and quality standards. Responsibilities: Keeps equipment operational by working with Management to coordinate maintenance and repair services; follows manufacturer's instructions and established procedures; requests special service. Reviews design documents related to procurement of new equipment; perform testing and operation of equipment. Prepare reports, charts, and tables based on established statistical methods to drive process enhancements such as tooling changes and in-process testing controls for management review. Evaluate, improve and validate current manufacturing practices or processes with an effort for continuous improvement towards productivity, quality, reliability and consistency. Assist in the development of manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment; conferring with equipment vendors. | 12/9/2020 |
| 9619 | Amneal Pharmaceuticals Branchburg Township , NJ QA Systems (Caliber) Coordinator BS in Relevant Discipline Exp: 1+ Years |
The Quality Systems Coordinator leads and reports data generation, data analysis and data interpretation. Create summary findings to support investigations, Corrective and Preventive Action (CAPAs), complaints etc. Monitors short-term and long-term effectiveness checks and monitors quality assurance trends related to Quality Management System (QMS) processes. Responsibilities: The QA coordinator will work collaboratively with users of quality system software on the collecting and distribution of reports related with quality documents. This includes coordinating and facilitating all aspects of planning, evaluation and reporting, problem resolution and solution to any quality issue. Performs evaluation of Change Controls in accordance with established procedures and ensures close out of these documents. Provides Quality Assurance (QA) management with timely data analysis and insights for potential corrective actions and improvements; and works collaboratively with QMS process owners, QA management and stakeholders to support quality improvement and data collection and organization. | 12/9/2020 |
| 9620 | Amneal Pharmaceuticals Brookhaven, NY Validation Engineer I BS in Pharmaceutical Manufacturing, Engineering, Science, or Relevant Field Exp: 1+ Years |
The Validation Engineer I provides support in performing equipment, facility and utility qualification activity and re-qualification activity to ensure compliance to cGMP and Amneal's quality requirements. Responsibilities: Assist in the preparation/ execution of Installation Qualification (IQ)/Operational Qualification (OQ)/ Performance Qualification (PQ) protocols for equipment, facility and utilities as well as related software. Help generate qualification report and help summarize the results which will be reviewed by the supervisor. Performs re-qualification of equipment, facility and utilities as required under supervision. Identify deviations encountered during IQ/OQ/PQ execution and work with supervisor to implement mitigation solution. Draft Standard Operating Procedure (SOP) for new operational equipment. | 12/9/2020 |
| 9621 | Amneal Pharmaceuticals Piscataway, NJ Scientist II, AR&D MS in Chemistry or Related Exp: 1+ Years |
The Scientist-2 is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. The individual in this capacity performs analytical methods qualifications/validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods and maintains/qualifies analytical equipment. Responsibilities: Performs analysis and release of active pharmaceutical ingredients, excipients, in-process materials, and finished drug products to support the formulation development team, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs. Develops and optimizes new and existing analytical methods for qualification and release testing of products. Develops stability indicating methods and performs methods validation. Provides timely responses to all internal and external inquiries. | 12/9/2020 |
| 9622 | Amneal Pharmaceuticals Piscataway, NJ Scientist II, Metrology/Quality Control MS in Chemistry or Related Exp: 1+ Years |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. Responsibilities: Performs chemical analysis of raw materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques, adhering to company policies as identified in standard operating procedures (SOPs). Prepares samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and analyzes. Creates and maintains laboratory record documentation (notebooks and computer-based), documents exact steps followed during analysis execution, calculates and reports results in a timely manner. | 12/9/2020 |
| 9623 | Amunix San Francisco, CA Lab Technicnan BS in Chemistry, Biology, or Related Exp: 1-2 Years |
The Lab Tech is responsible for supporting routine operations of the Fermentation and Purification Labs and completing routine laboratory procedures under the direction of the BioProcess Development and Manufacturing Lead. Other responsibilities: Conduct routine lab procedures (preparation of media and solutions, calibration of and testing with pH and conductivity probes, endotoxin testing, and good record keeping throughout). Weigh and mix specified components in calculated amounts, recording throughout. Set up and operate necessary equipment to support the above. Collaborate with manager, team members, and other functional groups at Amunix to plan, prioritize, and meet delivery deadlines. | 12/9/2020 |
| 9624 | A2 Biotherapeutics Los Angeles, CA Research Associate MS in Scientific Discipline Exp: 1+ Years |
The Therapeutic Technology team is seeking a highly motivated individual with experience in biochemistry, cell and molecular biology and assay development. The successful candidate will join us at our research facility in Agoura Hills, CA and work on cutting edge science in a dynamic, fast-paced and team-oriented environment. Responsibilities: The design, execution, documentation and presentation of biochemical and cell-based experiments. Development and implementation of novel assay protocol. Work with other scientists to design and perform cutting-edge immuno-oncology related experiments that integrate molecular biology, cell culture and assay techniques to develop treatments for multiple types of solid tumors. Collaborate with team members to select, profile and advance clinical candidates in a scientifically rigorous manner. Work under supervisor’s guidance both independently and collaboratively to implement novel laboratory processes and solve technical problems. | 12/1/2020 |
| 9625 | Abbott Irving, TX PCB Layout Engineer Preferred BS in Electrical or Mechanical Engineering, Material Science, or Related Exp: 6+ Months |
The PCB Layout Engineer will be working within a team environment to design and draft complex electronic PCB’s layouts and drawings. The qualified individual must be able to work in a fast-paced team environment and be responsible for schedules and deadlines. Responsibilities: Create footprints per supplier datasheets and IPC standards. Maintain and support Abbott eCAD Library. Layout of complex mixed-signal, mixed technology, high-density PCB designs. Provide full documentation for fabrication and assembly. Understanding pin mapping assignments in complex part symbols. Layout for placement and circuitry routing of PCBs for optimal electrical, EMI, thermal, and structural performance. Understanding of design rules constraint management and parasitic analysis. Use 3rd party tools to perform Design Rule Checks and insertion of test probes. Interface with Vendors and Suppliers to import and export data for fabrication of bare boards and installation of electronic and mechanical components. | 12/1/2020 |
| 9626 | Abbott Des Plaines, IL Scientist - Spectroscopy Lead (AMD) MS in Biophysics, Biochemistry, Physics or Biomedical Engineering ` Exp: N/A |
Abbott Molecular has an opening in its Des Plaines, IL site for a Scientist- Spectroscopy Lead who would conduct research for on-market product utilizing multiple experimental techniques. Responsibilities: Investigates and develops new procedures under the guidance of a research lead. Interacts with other groups and shares information; participates in team activities. Summarizes data and analyzes results, independently formulates conclusions, and determines future experiments. Actively participates in routine maintenance, lab safety; may assume roles of responsibility, such as training or document control. Prepares and delivers presentations of project results to others; presents data to larger and more diverse audiences. Teaches processes and problem-solving techniques. May lead others in project teams. | 12/1/2020 |
| 9627 | Abbott Abbott Park, IL Research Scientist BS in Chemistry, Biochemistry, Chemical Engineering, Biology, or Medical Technology Exp: 1+ Years |
Abbott Diagnostics has an opening for a Research Scientist. This qualified and motivated scientist will join a dynamic R&D team developing novel methodologies and assays for next generation diagnostic applications. These activities may also support the development of next generation instrumentation. This individual will help conceive, plan, design, and conduct advanced studies. The Research Scientist will investigate and develop new procedures. He or she will act as an independent contributor and will interact/coordinate with other groups and functions on project development and improvement. The successful candidate must have strong analytical and quantitative skills, as well as excellent oral and written communication skills. | 12/1/2020 |
| 9628 | Abbott Irving, TX Systems Engineer - Predictive Analytics BS in Electrical, Mechanical, Computer Science, or Systems Engineering or Related Exp: 1+ Years |
The Systems Engineer is responsible for understanding the integrated set of standards, sub-standards, and assemblies needed to design and manage systems over their life cycles. Applies an interdisciplinary, collaborative approach to plan, design, develop and verify a life-cycle balanced system of systems and system/subsystems solution(s) which satisfies customer/operational needs and public/regulatory acceptability. This includes a multitude of systems requirements that range from design, development, test methodologies, validations, risk analysis, documentation, and process improvements. | 12/1/2020 |
| 9629 | Abbott Abbott Park, IL Sr. Process Scientist - Fermentation MS in Chemical Engineering, Chemistry, Biology, or Biochemistry Exp: 1-5 Years |
The scientist will lead and consult on multiple complex projects defined for process investigations; design changes; resolving production issues and improving product availability and profitability. Leads a cross functional team with the required product/process knowledge to assess impact and develop plan. Focus will be in protein purification with one or more of fermentation, cell culture or recombinant protein experience. Other responsibilities: Demonstrate an understanding of the application of the Quality Policy through daily activities. Maintain vigilance to ensure adherence to the Quality Policy and system procedures by promptly reporting noncompliance issues to management. Develop and apply operations and process knowledge to area of support. Use sound judgment; appropriate scientific methods and thorough data analysis. Conceive; plan; design; execute; and document projects/activities efficiently and in conformance with applicable OPs. | 12/1/2020 |
| 9630 | Abbott Columbus, OH Analytical Assistant Chemist BS in Chemistry, Biology, or Closely Related Technical Field Exp: N/A |
Responsibilities: Conduct raw ingredient analyses which consist of simple titrations, moisture testing, organoleptic testing, sediment testing, etc. Conduct in-process and finished product testing including: determination for vitamins using various lab methods, protein and mineral analysis; fat by Mojonnier extraction technique, total solids determination, Iodide, chloride testing, and fatty acid profiles by Gas Chromatography per approved Laboratory Methods. Complete appropriate documentation and calculations needed for Standardization tests including: KOH, vitamin additions, final water calculations and physical tests such as pH, viscosity, grain color, and sensory evaluation. Complete housekeeping responsibilities such as washing glassware, waste disposal, general laboratory sanitation, etc. | 12/1/2020 |
| 9631 | Abbott Tampa, Fl Clinical Specialist I - CPT BS in Scientific/Technical Field Exp: 1-2 Years |
As a member of the clinical support team, you'll be responsible for providing technical clinical expertise and support of the sales process to colleagues, current customers and/or potential customers. Other responsibilities: Works under general direction with clinical and sales teammates to identify and capitalize on sales opportunities by creating competency, comfort and expertise with all Abbott Chronic Pain Therapies among physicians, support staff and customers within assigned geography. Performs work that involves a high degree of independence. Exercises independent judgment in planning, organizing, and performing work. Seeks to continually improve territory efficiency. Will begin to conduct PCP work and educational in services, as directed. Provides medical professionals with sales support, information, and training on the use of Company products and with staff education, in-services and technical troubleshooting. | 12/1/2020 |
| 9632 | AbbVie San Francisco, CA Associate Scientist II, In-Vivo Pharmacology MS in Relevant Field Exp: 0+ Years |
AbbVie is looking for an Associate Scientist II/Scientist I with experience in in vivo pharmacology study execution in various mouse models of cancer. The main role will involve conducting in vivo research studies from start to finish including tumor implantation, data collection, and data analyses. Additional opportunities to learn new skills and to work on ex vivo lab experiments will be provided as smaller roles, and based on project need and candidate’s interest. Above all, they are looking for a highly motivated and collaborative individual with a passion for oncology research, who enjoys working in a fast-paced and highly dynamic working environment. | 12/1/2020 |
| 9633 | AbbVie Branchburg, NJ Quality Control Technician II BS in Relevant Field Exp: 1-2 Years |
The Quality Control Technician II will be responsible for, but not limited to, performing inspections following procedures, specifications and applicable standards and regulations. Providing technical support to cross-functional teams as needed, identifies potential discrepancies and nonconformance and alert management. Performing porcine and human tissue receipt, and inspection, in-process inspections i.e. e-beam), and performing product discard as per procedures in an electronic data system. Ensuring proper equipment functionality and appropriate levels of supplies. Supporting and partnering with cross-functional teams to resolve any issues or non-conformance encountered. Assisting in documentation updates and related change controls activities as needed. Perform ing applicable actions for Nonconformance Reports (NCRs), Supplier Issues (SIs), Engineering Change Orders (ECOs), etc. | 12/1/2020 |
| 9634 | AbbVie Lake County, IL Associate Scientist II/Scientist I, Process Chemistry MS in Chemistry Exp: 0-2 Years |
AbbVie Process R&D is seeking a Chemist with strong synthetic skills. This individual will work under the mentorship of a supervisor to discover, develop, and execute routes to compounds that treat a variety of diseases. The candidate will be a member of an integrated Process Research & Development project team consisting of chemists (synthetic, structural, analytical) and engineers with the goal of identifying and developing novel and practical routes to newly discovered therapeutic targets. The ideal candidate will be enthusiastic and productive, with excellent communication skills and strong functional expertise in synthetic organic chemistry, compound synthesis, and characterization. Responsibilities: Independently design and conduct critical experiments that further project goals. Implement and may innovate new experimental protocols/techniques. Understand the goal and maintain a high proficiency in his/her projects as well as the overall program. Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments. | 12/1/2020 |
| 9635 | AbbVie Irvine, CA Scientific Associate BS in Chemistry, Biology, or Related Exp: 1-3 Years |
The candidate will have a critical role in supporting the overall Aesthetics Biological Research Program by managing inventory, administration of personnel training, and management of personnel security access. He/she will be the team Subject Matter Expert regarding a custom inventory database as well as policies and procedures for registration, use, shipment, and receipt of inventory. The candidate will coordinate and oversee inventory audits and will represent the team in interactions with EH&S and both internal and external auditing agencies. The candidate will identify and recommend changes in policies, procedures, and software design. He/She will coordinate shipment and receipt of samples, including entry of inventory into the electronic inventory system. Responsibilities will also include management of a freezer monitoring system. The candidate will also utilize a learning management system to administer and track personnel training on required SOPs. He/She will complete, submit, and manage security access requests for secured lab areas. In addition to the Biologic inventory responsibilities, the candidate will also support the team with protein quantification, SDS-PAGE, Western blot, and additional protein and DNA analysis, including documentation of results. Candidate will also partner with Departmental Lab Operations staff to escort vendors and service technicians during on-site visits into research labs. | 12/1/2020 |
| 9636 | AbbVie Lake County, IL Associate Scientist II/Scientist I, Toxicology Study MS in Scientific Discipline Exp: 0-2 Years |
This position sits within the Preclinical Safety group at AbbVie and reports to a senior manager in Toxicology. The Associate Scientist II / Scientist I, Toxicology Study Coordinator aides in the planning, conduct and reporting of non-GLP and GLP toxicology studies, acting to support the Study Director and regulatory infrastructure. Responsibilities: Draft study plans, amendments, and report components. Assist in the technical conduct of nonclinical studies including account set-up in electronic data capture system and scheduling of study events. Perform data review periodically through study conduct and at study completion. Facilitate communications among study personnel. Coordinate the archival of study data and specimens. Support GLP infrastructure through quality control responsibilities and active participation in process improvement activities. | 12/1/2020 |
| 9637 | AbbVie Lake County, IL Senior Safety Data Scientist MS in Health Sciences Field Exp: 1-2 Years |
This position partners with cross functional stakeholders in support of the product safety profile and benefit risk throughout product lifecycle through signal detection, signal evaluation, and preparation of written and verbal summaries of signal management activities and risks to patient safety to present to senior management and regulatory authorities globally. Responsibilities: Collaborates with safety and clinical teams to develop strategies and approaches for signal assessments and regulatory requests by analyzing data from multiple sources. Analyzes data to support signal assessment and contributes to ad hoc regulatory safety requests using data from multiple sources with supervision. Utilizes medical judgment to determine the impact of identified safety issues on the compound/ product’s benefit-risk profile. Communicates findings of surveillance activities and safety assessments to product teams and leadership to inform on necessary risk minimization activities, including label changes. Responsible for standard surveillance activities for a product’s life cycle (one or more assigned compounds and products) through review of safety data from clinical trials, safety databases, and the literature. | 12/1/2020 |
| 9638 | AbbVie Lake County, IL Combination Product Test Engineer MS or ME Exp: 0-5 Years |
Responsibilities: Execute test procedures and protocols supporting engineering testing and verification testing, analyze data, document in lab notebooks, and present results to cross-functional teams. Experience using Zwick and flow measurement equipment is preferred. Familiarity with 3D printing, CT Scanners, Viscometers, Climate Chambers, etc. is a plus. Define, develop, and validate test methods. Create verification plans, protocols, records, and reports. Support investigations and issue resolutions. Familiarity with DHR tools such as LinkUS, or Cockpit is desired. Experience with Solidworks, Minitab, Engineering Lab Notebook (ELN) is a plus. Expected to recommend improvements in design, processes, execution of a project or task as well as the maintenance of a program. Work in an independent manner under the guidance of a supervisor or technical lead. Assignments have clear and specified objectives. Complies with applicable policies and procedures, regulatory and safety requirements. | 12/1/2020 |
| 9639 | Abeona Therapeutics Cleveland, OH Associate, Process Development MS in Scientific Discipline Exp: 1-2 Years |
Abeona is looking for an Upstream Process Development Associate to join their team in Cleveland, OH. The successful candidate will be responsible for to support upstream process development initiatives and will be an integral part of a fast-paced group responsible for developing production processes for the manufacture of clinical AAV gene therapies. Responsibilities will include executing experiments across multiple scales from small shake flask cultures up to 200 L bioreactors. The ideal candidate will have some experience in production of biologics in either a research or development setting. Conducting research involving biochemical assays, effectively communicating results through high quality technical reports and oral presentations, and collaboration with your team is an integral part of this position. | 12/2/2020 |
| 9640 | AbSci Vancouver, WA Research Associate I/II Analytical Development and Purification BS in Analytical Chemistry, Biochemistry, Molecular Biology, Bioengineering or Related Exp: 1-2 Years |
The Research Associate I/II will play a significant role in analytical method development and characterization of therapeutic proteins expressed using SoluPro™, AbSci’s proprietary E. coli expression platform. Assays include, but are not limited to, protein concentration by A280, SDS-PAGE, Western blot, LC (e.g. LC-UV, SEC, IEX, etc.), CE-SDS, and/or LC-MS (e.g. intact mass, peptide mapping). Responsibilities: Independently perform laboratory tasks for the analysis of complex therapeutic proteins in lysates by a variety of different techniques, including SDS-PAGE, Western Blot, tip-based immunoassays, LC-UV, automated liquid handlers, MS, protein concentration, etc. Operation of sophisticated chromatography instrumentation, (e.g. automated liquid handlers, AKTAs, and HPLCs). Preparation of buffers, reagents, and other sample preparation techniques to support sample analyses. Operation of sophisticated chromatography instrumentation, (e.g. HPLC, MS, CE, etc.). | 12/2/2020 |
| 9641 | AbSci Vancouver, WA Research Associate , High-throughput Screening BS in Microbiology, Biochemistry, or Related Exp: 1-2 Years |
The Research Associate will be primarily occupied with executing a variety of high throughput assays. These include flow cytometry and cell sorting, ELISA, and plate based micro-fermentations. This position will be responsible for independently preparing media and buffers, processing samples, and preliminary analysis of results. Work will be done on a variety of automated hardware platforms including flow cytometers and liquid handlers. Candidate is enthusiastic about laboratory bench work, exhibits meticulous attention to detail, an eagerness to learn new techniques, and is comfortable working in a highly dynamic and rapidly scaling company. Responsibilities: Prepare needed buffers, stock solutions, and media. Independently execute strain screening experiments. Compile and enter data into the company’s LIMS system. Preliminary analysis of data to ensure operational integrity before handoffs to downstream groups. | 12/2/2020 |
| 9642 | AbSci Vancouver, WA Research Associate/Sr. Research Associate - Cloning MS in Molecular Biology, Biochemistry, Microbiology, or Related Exp: 1-2 Years |
The Research Associate/Sr. Research Associate, under direction of the Molecular Sciences team, will support innovative experimental research that advances AbSci’s proprietary E. coli SoluPro® expression platform. Primary responsibilities include providing core support to ongoing DNA construction, strain engineering, and NGS sequencing activities. The ideal candidate will demonstrate rapid mastery of assigned tasks and the capacity to take on additional technical responsibilities within an expanding team. | 12/2/2020 |
| 9643 | Absorption Systems Exton, PA Associate Scientist - Analytical Chemistry BS in Chemistry, Biochemistry, or Equivalent Exp: 0-2 Years |
As an Associate Scientist in the Analytical Chemistry Screening Department, you will work in a fast-paced environment with a team dedicated to helping our Sponsors select drug candidates to move forward in their pipelines. You will run various in-vitro screening assays related to helping understand how potential drugs overcome the biological barriers involved in getting to their ultimate target. You will work hands on with the latest technology in LC and MS systems to rapidly and efficiently analyze samples from these assays and provide our Sponsors the results they need in the time they need them. You will also prepare study protocols, analyze the data resulting from our various experiments, and prepare study reports to communicate those results to our Sponsors. | 12/2/2020 |
| 9644 | Absorption Systems Exton, PA Associate Scientist/Scientist - Molecular Biology (PCR and Cell Biology) BS or Higher in Molecular Biology Exp: 0-2 Years |
Skills: Knowledge and experience conducting experiments in some or all of the following areas (priority for more experience in PCR and cell biology): Cells culture and transduction/transfection in cells, extraction of DNA/RNA from cells and tissues, assays of transfection/transduction efficiency, and RT-qPCR and qPCR. Responsibilities: Preparation of assay protocol, planning and conducting of experiments under the direction of a senior scientist. Designing new PCR methods. Conducting molecular biology assays, such as RTqPCR and qPCR. Preparing and maintaining cell cultures and reagents. Transfection and transduction in cells. Documenting all results in laboratory notebooks. Writing reports for the study project under the direction of supervisor. | 12/2/2020 |
| 9645 | Absorption Systems Medford, MA QC Associate Minimum of BS in Biology, Chemistry, Pharmacology or Related Exp: 1-3 Years |
The QC Associate will work in a cGxP compliant Laboratory to support quality control of Bioanalytical and Bioassay Assay Validation and Sample Analysis. Responsibilities: Sample management including receipt, accessioning, logging, and storage. Critical reagent and supply management including receipt, inspection, and release for use. Review of Standard Operating Procedures (SOPs), Validation and Sample Analysis Reports, and individual data to assure the highest quality. Developing Word and Excel templates to improve and expedite data analysis and report writing. Reviewing logbooks for completeness and accuracy. Preparing data for archiving. Interacting with Principal Investigators, Scientists, QAU, and Management. | 12/2/2020 |
| 9646 | Absorption Systems San Diego, CA Research Associate BS in Pharmaceutical Sciences, Life Sciences, or Pharmacology Exp: 1-3 Years |
This position requires a broad knowledge of anatomy, physiology and biochemistry to help develop and support in vivo models to screen therapeutics and devices being developed for various disorders. Experience with surgical, dosing and sampling techniques is required. Prior experience working with other in vivo models may be considered even if there is no direct experience working with medical devices, stem cells or ophthalmology. Responsibilities: Participate in study design and preparation of preclinical studies. Fully support execution of preclinical studies. Help in the preparation of study protocols and reports. May be required to serve on the Institutional Animal Care and Use Committee (IACUC). Interface with different teams including in vivo scientists, QC/QA, Account Managers/Sales. Maintain accurate records in various internal databases. | 12/2/2020 |
| 9647 | Absorption Systems San Diego, CA Research Associate, Formulations BS in Relevant Field Exp: 1-3 Years |
Responsibilities: Perform preparation of test article/substance dosage solution/suspension(s), ensure preparation procedures and calculations are standardized, performed consistently and recorded correctly by the technical personnel. Receive all incoming test articles/substances and reagents. Ensure that the documentation for the use of all test articles/substances and vehicles/reagents to ensure consistency and correctness. Sampling and the shipment of formulation samples. Maintaining cleanliness and general appearance of the Formulations Laboratory. Ensure that test article/substance(s) from completed studies are returned to the sponsor as needed. Responds to Quality Assurance audits of preparation procedures and calculations. Maintaining an up to date inventory of reagents, test article/substance, vehicles and samples. Review chemistry data for submission at completion of study. Prepare accurate packing list for the shipment of test article/substances and samples to the sponsor and/or analytical laboratory. Notify appropriate personnel of shipments. | 12/2/2020 |
| 9648 | Absorption Systems Exton, PA Scientific Account Manager - Drug Development MS in Pharmaceutical Sciences, Life Sciences, or Pharmacology Exp: 0-1 Year |
Absorption Systems, a preclinical Contract Research Organization located in Exton, Pennsylvania, is seeking a candidate for a Scientific Account Manager position. Scientific Account Managers (SAMs) are key members of the Absorption Systems Sales Team and function as liaisons between sponsors, internal research scientists, study directors, and business development team members. AMs use their knowledge of preclinical drug testing to design and manage studies for a wide range of sponsor requests ranging from lead optimization through regulatory submissions. Responsibilities: Design studies that meet sponsors' needs in a scientifically sound and cost effective manner. Address customer requests for information promptly and accurately. Follow internal processes for accurate record keeping of study designs, proposals, and pricing logic. Rapidly increase knowledge of preclinical drug testing to enable peer-interactions with clients. | 12/2/2020 |
| 9649 | Absorption Systems Exton, PA Scientist/Sr. Scientist - Molecular Biology MS in Molecular Biology, Biochemistry, Microbiology, or Related Exp: 0-2 Years |
Responsibilities: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. New PCR design. Conducting studies on molecular biology assays, such as RT-qPCR and qPCR. Preparing and maintaining cell cultures and reagents. Transfection and transduction in cells. Documenting all results in laboratory notebooks and presenting research data in group and other meetings. Project study report writing under the direction of supervisor. Cell culture and transduction/transfection in cells. Extract DNA/RNA from cells and tissues. Perform assays of transfection / transduction efficiency. RT-qPCR and qPCR. | 12/2/2020 |
| 9650 | Associates of Cape Cod Falmouth, MA Quality Control Analyst I BS in Relevant Scientific Discipline Exp: 0-2 Years |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 12/2/2020 |
| 9651 | AccuraGen Menlo Park, CA Research Associate/Senior Research Associate BS/MS in Biology or Related Exp: 1+ Years |
AccuraGen is looking for a highly motivated research associate to join their Assay Development team. The assay development team is developing a library preparation platform that will provide the most diverse analysis of multiple analytes in plasma. It will deliver unparalleled accuracy of cancer detection from a minimal amount of patient blood samples. Responsibilities: Plan, execute and interpret experiments. Analyze data, evaluate results, form conclusions, and recommend future experiments. Ensure accurate and consistent recording of experiment methods, materials and results; keep a high-quality laboratory notebook. Communicate and work efficiently with other groups within R&D team. Adjust work schedule to meet time-sensitive project milestones. | 12/2/2020 |
| 9652 | AccuraGen Menlo Park, CA Scientist I, Research and Development MS in Molecular Biology Exp: 1+ Years |
AccuraGen is developing systems that will provide the most sensitive, accurate, and robust NGS-based ctDNA mutation detection. It will deliver unparalleled accuracy from a minimal amount of patient blood samples. They are looking for an outstanding individual to join their R&D team to drive technology innovation, product development and commercialization. Responsibilities: Plan, design and execute assay research and development experiments. Analyze data, evaluate results, form conclusions, and provide and/or implement improvements. Communicate results with colleagues and R&D management. Ensure product performance by utilizing proven development practices and/or developing novel procedures to overcome obstacles. Optimize and document SOPs to achieve commercial levels of stability, robustness and performance. | 12/2/2020 |
| 9653 | Acellapharma Alpharetta, GA Customer Complaint Quality Coordinator BS in Scientific Discipline Exp: 1-3 Years |
The customer complaint quality coordinator will be the first point of quality contact for Acella and Avion complaints and ensure that complaints are managed in accordance with site SOP and regulatory guidance. Responsibilities: Record and monitor consumer complaints in a validated document management system. Triage and initiate investigation requests with both internal team and external suppliers. Provide a written response to the consumer/customer stating the outcome of the investigation along with the pharmacovigilance guidance as needed. Work and assist medical advisors as needed. Generate a MedWatch report as a result of a serious adverse event. Respond to technical queries related to the products. Assist the Drug Safety management or delegates as required. Work with pharmacovigilance service providers as required. | 12/2/2020 |
| 9654 | PharmaSeek LLC Cary, NC or Madison, WI, Clinical Research Analyst BS/MS in Scientific or Mathmatic Discipline Exp: N/A |
The Clinical Research Analyst is responsible for assisting research institutions with budget development and negotiation, coverage analysis, and clinical trial management system services. The Clinical Research Analyst will complete these critical functions in a manner designed to expedite the conclusion of the start-up process for our clients while maintaining a high level of quality. They are in need of critical thinkers to help interpret Medicare/Medicaid guidelines, analyze clinical research protocols, and work directly with our clients to develop and negotiate clinical trial budgets. Responsibilities: Interpret Medicare/Medicaid coverage decisions and national guidelines to determine what procedures are billed to the sponsor and which are billed to Medicare/private insurance. Identify appropriate research modifiers to be placed on claims. Develop and negotiate clinical trial budgets based on client’s preferred pricing methodologies. Build studies within client’s clinical trial management system (CTMS). Work with Senior Clinical Research Analysts and Manager to review and alter deliverables as needed. | 12/2/2020 |
| 9655 | KMR Group INC Chicago, IL Data Analyst BS in Engineering, Mathmatics, or Sciences Exp: 1-3 Years |
The Data Analyst plays a critical role and is responsible for turning data into information, information into insight, and insight into business decisions. The primary responsibilities include data analysis, data management, data operations, and application validation. Other responsibilities: Manage raw data, query, and create databases using Excel. Construct data frameworks for analyzing data; analyze data using standard methods as well as statistical methods, interpret results, and present clear summaries. Visualize data using Excel and Visio. Interpret data analysis and write reports. Assist in the development and delivery of data analysis packages for client data services. | 12/2/2020 |
| 9656 | Acumed Hillsboro, OR Product Engineer 1, Sustaining (Medical Device) BS in Mechanical or Bio-Mechanical Engineering, or Equivalent Exp: N/A |
The Product Engineer, Sustaining is responsible for products after development is completed and when they are released for commercialization. This includes supporting manufacturing, quality improvements, product analysis on field complaints, document Remediation, biocompatibility of raw materials and final products, additional testing required by regulatory bodies for follow on regions and supporting product training to surgeons as needed. When needed, the Product Sustaining Engineer also participates on new product development teams and/or product update and extension projects. All of these efforts involve research, planning, idea creation and realization, concept development, specification generation, testing and validation protocols, as well as effective communication with team members, management, and customers. | 12/2/2020 |
| 9657 | Adaptimmune Philadelphia, PA Quality Control Associate BS in Relevant Field Exp: 1-3 Years |
The Quality Control Associate will be responsible for conducting in-process and finished product testing associated with Adaptimmune clinical trial material. In addition, the role will be working with other departments for deviations and method transfers. Responsibilities: In-process, finished product and stability testing of clinical trial material. Maintenance of Quality Control Protocols, SOP’s and Test Methods. Deviations, change controls, CAPAs. Method / Technology Transfer of existing methods into the Adaptimmune QC Lab | 12/2/2020 |
| 9658 | Adaptive Biotechnologies San Francisco, CA Research Associate II MS in Cell Biology, Immunology, Genetics, Biochemistry, Bioengineering, or Molecular Biology Exp: N/A |
Adaptive Biotechnologies is currently recruiting a Research Associate II to join their TCR Discovery team. The successful candidate will work as a part of a team using cellular assays to screen, characterize and develop T cell receptors as potential therapeutic agents. Responsibilities: Isolate and culture human primary immune cells and cell lines. Transfect mammalian cells, as well as optimize and troubleshoot transfection protocols. Use flow cytometric assays to characterize the specificity and potency of T cell receptors, and assess their potential utility as anti-tumor (or alternative disease) therapies. Take initiative in improving current assays to streamline processes. Assist with pre-clinical studies, using GLP techniques and documentation. Assist in the design and development of new cell based assays as the need arises. | 12/2/2020 |
| 9659 | Adaptive Biotechnologies Seattle, WA Accessioning Specialist II BS in Biology or Related Exp: 1+ Years |
The Accessioning Specialist II position will join the Biological Sample Management (BSM) group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support sample management and chain of custody for Adaptive’s immunosequencing services that includes research, clinical projects, and diagnostic testing. Responsibilities: Enter, upload and ensure accuracy and completeness of information pertaining to samples and related projects through multiple systems. Ensure there is a record of every system transaction relating to each managed sample in order to evidence sample Chain of Custody (COC). Ensure appropriate inventory management (freezer management) of each physical sample through the entire sample management lifecycle. | 12/2/2020 |
| 9660 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I - PCR BS/MS in Chemical, Physical, or Biological Science Exp: 1+ Years |
The Clinical Laboratory Technologist 1 position will be responsible for processing medically relevant biological samples through extraction or high throughput DNA sequencing assays. This role will work within a team of Laboratorians in a fast-paced, high production setting to process research and clinical diagnostic samples to provide a test result to patients, oncologists and other medical practitioners and researchers. As such, high attention to detail and clinical mindedness are crucial to success in this role. Responsibilities: Assignment to one of two labs performing either DNA extractions from human biological samples, or PCR amplification and high-throughput sequencing assays on DNA libraries. Demonstrate good clinical judgment and integrity. Perform DNA extractions, PCR amplification or high-throughput sequencing assays on DNA libraries. Perform protocols under compliance with regulatory agencies; model appropriate clinical, regulatory and safety practices. | 12/2/2020 |
| 9661 | Adaptive Biotechnologies Seattle, WA Principal Quality and Regulatory Affairs Engineer BS/MS in Relevant Scientific Discipline Exp: 1+ Years |
This position is responsible for developing software processes to ensure that software development practices comply with applicable regulatory requirements, as well as supporting day to day quality operations and processes supporting software engineering efforts at Adaptive. This position is accountable for ensuring that the Adaptive SDLC is both efficient as well as compliant with applicable international (IVDD/IVDR), Federal (21CFR), and other applicable regulations. In addition, this position is responsible for maintaining quality processes such as assisting in Nonconformance and CA/PA investigations and actions. The position requires the ability to manage priorities from multiple projects and tasks utilizing effective written and oral communication skills. Will apply quality and regulatory systems knowledge, problem solving and judgment skills to ensure the appropriate balance of quality, compliance and business needs. | 12/2/2020 |
| 9662 | ADIMAB Lebanon, NH Research Associate - Antibody Sciences BS/MS in Molecular Biology, Biological Engineering, Cellular Biology, or Related Exp: 1+ Years |
The Research Associate will work in a small team to isolate and characterize antiviral antibodies from primary human B cells for research studies and therapeutic development. The Research Associate will also work on technology development projects to improve Adimab’s antibody discovery pipeline. Responsibilities: Basic handling and culture of yeast and mammalian cells. Primary B cell isolation using fluorescence activated cell sorting (FACS). Single-cell RT-PCR. Quantification of antibody responses via ELISA. Construction and selection of yeast antibody libraries. Mammalian cell based characterization assays. Collection, organization, analysis, and presentation of data. Tracking and upkeep of lab reagents and stocks. Facilitate collaborations with internal and external colleagues. | 12/2/2020 |
| 9663 | ADMA Biologics Boca Raton, FL QA Specialist I - Product Release BS in Relevant Field Exp: 1-2 Years |
Responsibilities: Understand the cGMPs and processes such as Quality Systems (e.g., Deviations, Corrective and Preventive Action reports {CAPAs}, Change Controls, and Out of Specifications {OOSs}). Ensure cGMP and regulatory compliance as defined in government regulations such as 21 CFR Parts 11, 210, 211, and 600, as well as compliance with corporate policies and procedures. Review and release manufacturing batch records, and any additional supporting documents including but not limited to logs, charts, specifications, and environmental and WFI data. Perform usage decisions for batch release in SAP. Work with IgG Manufacturing floor personnel and other technical operation departments to resolve documentation and compliance issues. Perform period follow-up of ongoing deviations to assure timely closure of documentation and batch release. Review and approve Certificates of Analysis for batch release in LIMS. Review SOPs and documents from other departments and provide feedback as necessary. Perform review and release of Plasma pools when required. | 12/2/2020 |
| 9664 | Trevigen Minneapolis, MN Advanced Quality Technician Minimum of Associates Degree Exp: 1-3 Years |
The responsibilities of an Advanced Quality Technician are to perform tasks in the process of inspecting and testing science products. Duties may require interpreting results, equipment operation, inventory, participation in complaint investigations and calibrating equipment. This position will participate in the continuous improvement of our products and customer-centered culture. The technician will also: conduct inspections of raw materials, intermediates and finished goods to ensure specifications and quality standards are met with minimal instruction and supervision, conduct inspection of product literature and labels to ensure accuracy, pay much attention to detail, reconcile documents, compile, analyze and report on data of moderate complexity, and consistently advocate for Quality Ideals by demonstrating commitment to meeting quality requirements in daily work | 11/18/2020 |
| 9665 | Trevigen Minneapolis, MN Advanced Research Associate Masters Degree Exp: Up to 2 Years |
This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. Participate in troubleshooting as needed. Responsibilities: perform routine bioassays following the instructions for quality control on proteins, antibodies, and related products, perform more complex bioassays following the instructions for quality control on proteins, antibodies, and related products, analyze and report data with the consideration of intra and inter-assay variations and other factors which may affect the assay results, keep accurate records of all experiments performed, follow GMP guidelines, documentation, and workflow, maintain cell lines; isolate primary cells from human/animal blood and animal tissue for use in bioassays, freeze cell stock for future applications. | 11/18/2020 |
| 9666 | Trevigen Devens, MA Manufacturing Technician - Filling (INTERNSHIP) Bachelors Degree Exp: 0+ Years |
The Manufacturing Technician is responsible to operate manufacturing equipment and complete all documentation according to cGMP/ISO standards. Provide written documentation of required data throughout the manufacturing operations in accordance to established SOPs, Work Instructions and cGMPs/ISO standards. Provide hands on assistance as needed on equipment lines and manual pack lines. They will also need to understand and follow appropriate standard operating procedures and work instructions such as the regulatory awareness of chemical handling and hazards, labeling, safety procedures, department specific SOP’s, and proper use and basic equipment maintenance. | 11/18/2020 |
| 9667 | Trevigen Newark, CA Research Associate, R&D BS in Molecular Bio, Biochem, Cell Bio, or Related Exp: 1+ Years |
The research associate will work within a highly dynamic group and be responsible for developing new products and applications for RNAscope technology. Responsibilities: Execute RNAscope/BaseScope-based assays to support new product development and assay optimization, including but not limited to BaseScope manual assay testing, R&D collaboration projects and RUO raw material improvement projects. Support manufacturing QC for commercial product testing, release and troubleshooting when needed. Facilitate SOP/SPK/SPJ drafting/assay QC procedure transfer from R&D to QC team. Participate in R&D/QC communication and hands-on training. Responsible for experimental design, assay running, data collection and interpretation. | 11/18/2020 |
| 9668 | Trevigen Wallingford, CT Bioinformatics Scientist MS in Bioinformatics, Computer Science, Engineering, or Related Exp: 1-3 Years |
They are currently looking for a Bioinformatics Scientist in a multi-role as data analyst, developer, and bioinformatics scientist to support the Simple Plex BU. Experience or coursework with biological sourced data analyzed using various techniques including statistical analysis, machine learning, and data visualization are required. They are looking for a motivated, cross-disciplinary individual to implement novel approaches in data analytics for the purposes of delivering actionable intelligence for assay development, manufacturing, QC, product support, and engineering. Responsibilities: Assist with exploratory analysis of Simple Plex assay data from QC, product support, and R&D projects. Work with biologists, engineering, and product support, to create visualizations and analysis. Drive informed decision making for product development, QC, operations. Establish code and data control process to enable multi-user collaboration across functional areas | 11/18/2020 |
| 9669 | Trevigen Cambridge, MA Research Associate (Protein Purification) BS in Related Field Exp: Up to 3 Years |
They are seeking a protein biochemist who will contribute to the ongoing research and development of products including complex assay systems, post-translationally modified proteins and peptides, and recombinant enzymes. The candidate will have previously purified proteins from bacterial, insect, and/or mammalian expression systems, and will have theoretical knowledge or hands-on experience with isolation of proteins from prokaryotic and eukaryotic organisms. Responsibilities: carry out troubleshooting activities under supervision, collaborate with other departments/labs as needed, follow guidelines and comply with all company safety, quality, and training procedures and regulations. | 11/18/2020 |
| 9670 | Trevigen San Marcos, CA QC Specialist BS in Biological Science, Chemistry, or Related Exp: 1-5 Years |
Responsibilities: Performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. Coordinate, perform and maintain QC testing and scheduling for Stability program. Assist in establishing QC specifications. Assist in the validation testing of equipment and processes. Assist in the review and creation of ISO/QSR documentation. Perform QC assay testing for release of final product. Perform assay testing for Value Assignment, complaints and date extensions. | 11/18/2020 |
| 9671 | Trevigen Newark, CA Research Associate, R&D BS in Molecular Bio, Biochem, Cell Bio, or Related Exp: 1+ Years |
They seek a highly motivated and creative Research Associate to join the R&D team. You will work within a highly dynamic group and be responsible for developing new applications for RNAscope technology and support our assay services business. Responsibilities: Execute Custom Assay Services (CAD)/PAS projects, including but not limited to ISH-IHC, pre-project proof of concept/probe validation, troubleshooting and others. Focus will be ISH-IHC and new application development to support ISH business expansion and accumulate more in-house experience for new technology development. Responsible for experimental design, assay running, data collection and interpretation. | 11/18/2020 |
| 9672 | Trevigen Minneapolis, MN Advanced Research Associate Masters Degree Exp: Up to 2 Years |
The major responsibilities of this position are to primarily develop plate-based ELISA products related to Bio-Techne's existing product lines, including literature review, data analysis, reagent evaluation, feasibility, assay optimization, stability studies and product transfer. Additional work on protein chemistry, antibody evaluation and collaboration with other internal development teams may be needed. Other responsibilities: Develop new immunoassay products. Under general supervision, independently schedule, plan, perform and report experiments for the feasibility, optimization, transfer and validation of immunoassay kits. Evaluate critical raw materials. Optimize formulations and procedures to meet all assay specifications. Understand biological attributes of assay targets by reading literature and defining design goals. | 11/18/2020 |
| 9673 | Trevigen Devens, MA Advanced Quality Technician Science or Quality Related BS Exp: 1+ Years |
Advanced Quality Technician reports to the Quality Control Manager and is responsible for in-process and final QC testing of Bionostics products. In addition, Advanced Quality Technician participates in instrument validations, performs lab maintenance activities, initiates collaborations, monitors laboratory and process inventories, conducts device history record review, and creates certificates of analysis for commercial products. Responsibilities: Understands and adheres to all quality technician job requirements. Follows work instructions carefully and demonstrates good documentation practices. Documents results, processes testing, and refers to past batch records when needed. Compiles, analyzes and reports on data conformity | 11/18/2020 |
| 9674 | Trevigen Minneapolis, MN Advanced Research Associate - Molecular Biology MS in Molecular Bio, Cell Bio, or Equivalent Exp: 0-2 Years |
The responsibilities of this position are to assist the protein product development team in recombinant protein expression. This includes the preparation of eukaryotic expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, mammalian and insect cell culture, transfections, Western blotting, ELISA, and flow cytometry. | 11/18/2020 |
| 9675 | Ultivue Cambridge, MA Laboratory Technician (Assay Development) Minimum of BS in Chemical, Physical, Biological, Clinical Lab Science or Related Exp: 0-1 Years |
The laboratory technologist will support contract research offerings as part of Ultivue’s Assay Development and Services Laboratory. Laboratory work utilizes Ultivue’s InSituPlex™ technology for fluorescence multiplex IHC (mIHC). The lab technician will support routine testing and QC procedures. Technician may take part in basic assay optimization and multiplex panel development activities to support services and U-VUE kits offerings. Responsibilities: Follow laboratory protocols and safety regulations in accordance to a quality management system (QMS). Edit SOPs in continued effort towards regulatory compliance. Perform routine logging of specimens and documentation of sample testing into Ultivue’s laboratory management information system (LIMS). Perform related laboratory maintenance, such as ordering supplies, managing inventory, managing and maintaining equipment, and documenting laboratory conditions. Perform routine and testing of InSituPlex™ assay utilizing specific standard operating procedures (SOPs). Assist pathologist and Ultivue scientific staff in imaging and test support. | 11/25/2020 |
| 9676 | Ultivue Cambridge, MA Document Control Specialist BS in Biology or Related Life Science Exp: 1+ Years |
The Document Control Specialist will support the Quality Management System (QMS) by assuring that all controlled documentation for products are in compliance with current Good Manufacturing Practices (FDA), ISO 13485, EU and Health Canada regulatory requirements, as required and will report into the Senior Director of Quality & Regulatory. Responsibilities: Under the direction of the Head of Quality, the Document Control Specialist is responsible for supporting all documentation and training needs. Lead Ultivue’s training program for all employees by monitoring, scheduling, and documenting training. Train new Quality Assurance staff as needed. Provide documentation and training coordination services including numbering, version control, formatting, processing, and filing of documents. Create training profiles, update training profiles on paper and in electronic system, create training reports, maintain training records, etc. | 11/25/2020 |
| 9677 | Getinge Wayne, NJ Complaints Analyst I BS in Related Science or Technology Field Exp: 0+ Years |
Responsibilities: Work in a team environment with members of the SSU and QA-Product Surveillance groups on receiving complaints in the complaint system. Work in a team environment with members of the Engineering and Medical teams on completion of Decision Tree (DT) and completion / submission of Initial MDRs. Work independently and with different parts of the organization/departments to perform Good Faith Effort (GFE) to obtain required / additional event information and request sample return. Ensure complaints are handled in compliance with applicable regulations and regulatory standards. Accountable for compliance with all Food & Drug Administration (FDA) and European Union Medical Device Directives (MDD) regulations governing adverse event reports such as Medical Device Reports (MDR) and Medical Device Vigilance (MDV) and reportability requirements for various countries. | 11/25/2020 |
| 9678 | Vaxart San Francisco, CA Quality Control Analyst I BS in Scientific Discipline Exp: 0-1 Years |
QC Analyst I is responsible for performing drug substance and drug product in-process, release, and stability testing activities in support of CGMP manufacturing of clinical trial materials. This candidate will also be responsible for providing support to R&D for analytical development and other activities as assigned by supervisor. Other responsibilities: Provides QC support to development and manufacturing in the form of CGMP assay support involving release and stability testing. Performs product characterization activities, including: potency assays, drug product physical characterization, and stability assessment. Performs work necessary to implement procedures appropriate for analysis of drug substance and drug product clinical trial and development materials. Maintains the QC laboratory. | 11/25/2020 |
| 9679 | Vaxcyte Foster City, CA Associate Scientist/Engineer, Polysaccharide Process Development BS/MS in Bioprocess Engineering, Chemical Engineering, Microbiology, or Related Exp: 1+ Years/0+ Years |
Vaxcyte is looking for an energetic and talented associate scientist/engineer to contribute to the Polysaccharide development and manufacturing group within the CMC team. Vaxcyte is developing a multi-valent polysaccharide-based conjugate vaccine, based on a novel carrier protein produced using the Xpress CF platform. Polysaccharides are a critical component in conjugate vaccines. The successful candidate will have some practical laboratory experience developing processes related to fermentation, microbiology, biopharmaceuticals, or vaccine industries. The candidate will be eager to utilize and learn new laboratory skills as this person will be responsible for collaboration on experimental design and execution of experiments to further the polysaccharide development program. This position will require >60% time in the lab and this person will be able to independently detail experimental procedures/results to colleagues. The successful candidate will work within the polysaccharide development team to design and execute experiments, summarize pertinent data and present experimental results internally. | 11/25/2020 |
| 9680 | VGXI Woodlands, TX Process Technician BS in Life Sciences Exp: n/a |
Responsible for the implementation of cGMP in the pilot plant. Write and review SOPs and production batch records. Implement production processes for the manufacture of plasmid DNA. Conduct cGMP production of plasmid products on an ongoing basis. Other responsibilities: Manufacture plasmid DNA conforming to GMP guidelines. Assist in scaling-up processes to meet growing demands. Write standard operating procedures. Execute validation protocols. Prepare solutions and materials required for the process. Follow batch records or SOPs to conduct cell banking, fermentation and purification processes for plasmid DNA manufacture at research or GLP scale. Conduct miniprep, concentration and gel analysis to in-process samples of research and cGMP productions. | 11/25/2020 |
| 9681 | ViaCyte San Diego, CA Manufacturing Associate I BS/MS in Biological or Engineering Science Exp: 1+ Years |
The incumbent will perform a broad range of tasks in the cGMP manufacture of cells and combination cell therapy/device products for use in clinical and developmental studies. This position includes hands-on participation, including materials logistics, assisting in manufacturing operations, and may include non-routine development activities. This is a full-time position. Requirements: Assist in manufacturing operations to produce GMP grade PEC-01 and Combination Product to meet corporate goals. Assist in ensuring that there are sufficient materials available for all production runs or campaigns, including media, small molecules, and growth factors. Provide hands-on support for scale-up and development activities as needed based on a demand plan. Understand and review applicable GMP documentation, including batch records, SOP’s, deviations, change requests, CAPA’s, IOQ’s, technical reports, and other documents. Maintain current training status for all applicable activities. Assist in maintaining GMP areas in a constant state of inspection readiness related to equipment and area preventive maintenance, calibration, and certification. Throughout the course of all job activities, maintain accurate records and documentation required to support regulatory submissions, and comply with regulatory requirements. | 11/25/2020 |
| 9682 | Vivex Biologics Miami, FL Process Engineer I BS in Biomedical Engineering or Other Applicable Engineering Discipline Exp: 1-3 Years |
The Process Engineer I is responsible for evaluating and improving manufacturing processes to reduce cost, improve yields and reduce variation. This position performs equipment qualifications and process validations. Process Engineers also participate in technology transfer to ensure the processes necessary for new products are effectively translated to manufacturing from R&D. Process Engineer I makes use of statistical analysis methods, critical thinking, process development, and scaling principles to achieve the objectives mentioned above. Other responsibilities: Generate and execute protocols to perform equipment qualifications and process validations. Use LEAN Manufacturing principles to analyze processes and make recommendations for improvements. Lead efforts to solve problems using formal problem resolution techniques and root cause analysis. Create and communicate project plans with detailed tasks and timelines necessary for project completion. | 11/25/2020 |
| 9683 | Vivex Biologics Miami, FL Tissue Processing Technician I College Degree in Related Field Preferred Exp: 1+ Years |
The Tissue Processing Technician I supports the Tissue Processing Supervisor in the cleaning, cutting, shaping, inspecting, and packaging of tissues for transplantation. The Tissue Processing Technician I is also responsible for complying with the quality assurance requirements and quality system goals of the bank as mandated by federal, state, and trade regulations. Other responsibilities: Preparation of clean room and clean room procedures as specifically described in SOPs. Preparation of aseptic processing, environmental set-up including all equipment supplies and monitoring of sterile rooms. Processing of all allografts for clinical such as bone, soft tissues, skin, autografts and other tissues as instructed by Processing Supervisor or designee. Preparation and preservation of all types of bone for cutting and shaping into allografts. | 11/25/2020 |
| 9684 | Vivex Biologics Miami, FL Donor Development Coordinator BA/BS in Medical Field Exp: 1-3 Years |
The Donor Development Coordinator acts as a donation specialist facilitating the potion of tissue and eye donation. Works as a liaison between the Donor Referral Center and Medical Examiners Offices, law enforcement agencies, and hospitals to ensure quality tissue is recovered. Responsibilities: Works directly with the Donor Services representatives & Donor Management Coordinators on a scheduled or emergency basis and evaluates potential donors by contacting hospital staff and collecting and reviewing all relevant medical records to properly screen a donor and to determine suitability. Approaches NOK of potential donor to request tissue donation. Completes Authorizations and conducts/documents DRAI Interviews with the NOK/designated historian according to FDA Regulations, AATB Standards, and UMTB Donor Services Foundation protocols and policies. Completes all required case paperwork and documents and insures delivery of said paperwork to appropriate departments and triage donor per protocol and per the wishes of the donor and/or donor's family. | 11/25/2020 |
| 9685 | Vivex Biologics Miami, FL Product Service Specialist BS in Related Healthcare Field Exp: 1+ Years |
Responsible for the delivery of superior customer service through the use of effective communication and coordination in the receipt, processing, and placement of allograft tissue orders from customers and/or distributors of the tissue bank. Handling allograft orders demands a great deal of attention, detail orientation, and management of time to ensure that allografts reach the desired destination. Builds and maintains business relationships with clients by providing prompt and accurate service to promote customer loyalty to Vivex Biologics, Inc. Other responsibilities: Serves as the first point of contact for general inquiries such as pricing, product availability, and allograft-related technical questions. Ability to identify customer needs and offer product substitutions based on surgical procedures or historical data. Responsible for initiating calls to existing and potential customers to generate revenue for direct distribution. Coordinates the demands and needs of international distribution commitments of the tissue bank to include, tissue allocation, request for tissue production, shipping/customs documentation, and certificate of conformance (if applicable). | 11/25/2020 |
| 9686 | Wave Life Sciences Cambridge, MA Associate Scientist, Medicinal/Organic Chemistry MS in Chemistry or Related Field Exp: 0-3 Years |
WAVE Life Sciences is seeking a highly motivated synthetic organic chemist to join its medicinal chemistry team in Cambridge, Massachusetts. This is an ideal position for an individual who is interested in learning cutting edge technologies and who thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate will be responsible for planning, designing and executing multi-step synthesis including purification and compound characterization. Collaboration with colleagues across disciplines, participation in project team meetings, and contribution toward creative problem solving are all encouraged. Other responsibilities: Under general supervision, perform multi-step organic synthesis, operates scientific equipment and instruments, analyze data and prepares related reports. Familiar with the operations involving large scale synthesis. Maintain detailed records of experimental protocols and data in accordance with company policy. Presentation of results in both written and oral format and delivery of completed reports within a multidisciplinary team. | 11/25/2020 |
| 9687 | CROWN Johnson City, TN QA Specialist BS in Scientific or Related Discipline Exp: n/a |
The QA Specialist is responsible for performing Quality compliance activities on the plant floor and ensuring that all activities are in compliance with company and regulatory guidelines and procedures. In addition, the QA Specialist is also responsible for assisting in activities directly related to batch release, and batch record and procedure review, revision and approval. The QA Specialist is required to consult with the Quality Management on all serious issues that may impact the company or product. | 11/25/2020 |
| 9688 | CROWN Johnson City, TN QC Analyst/Chemist BS in Chemistry Exp: 0-3 Years |
The QC Analyst is responsible for performing testing of raw materials and components, finished products, and stability samples as well as in process tests. In addition, the Analyst is also responsible for assisting in the maintenance and calibration of analytical instruments, preparation of standard and sample solutions and maintenance of associated records. Other responsibilities: Position requires familiarity with HPLC, GC, UV-Vis, IT, and titration as well as standard wet chemistry including, but not limited to, viscosity, pH, etc. Position will also perform peer review of other chemists work and take part in the training program as requested. Position will also be responsible for helping to create and update procedures and documentation for performance lab related activities. Perform investigations as required in accordance with company and regulatory guidelines. | 11/25/2020 |
| 9689 | CROWN Dallas, TX Medical Affairs Specialist BS in Medical Related Field or Life Science, Graduate Degree Preferred Exp: 1+ Years |
The Medical Affairs Specialist collaborates with members of cross-functional teams to prepare high-quality correspondence, study protocols, investigator brochures, synopses, regulatory documents, medical and clinical publications, and related medical and clinical documents within agreed-upon timelines. Responsibilities: Prepares, edits, and finalizes protocols, medical affairs scientific presentations, abstracts, manuscripts, and correspondence. Participates in scientific communication planning, including development of strategic medical communication plans, publications in Medical and Scientific Journals, online webinar content creation. Supports the writing, review, and edit of Marketing and Medical Affairs/Clinical Development materials. Partners with the study biostatistician to engage early with the study team including participation in the review of mock and/or blinded tables, figures, and listings (TFLs), and narrative planning for relevant documents. Works closely with the study team to ensure that results and messages in clinical documents accurately reflect the data in TFLs and other information sources. | 11/25/2020 |
| 9690 | UBC Blue Bell, PA Safety Data Associate BS in Science or Health Related Field, Pharmacy or Nursing Exp: n/a |
This position is primarily responsible for supporting all operational functions within the Global Pharmacovigilance department. Other responsibilities: Is responsible for the monitoring on a daily basis of the PV mailboxes, fax machines sharepoints/portals and acknowledging receipt of safety case reports. Is responsible for Book-in, duplicate check and accurate full Data Entry of safety case reports into safety database in a timely manner. Generates draft case narrative as assigned by UBC PV Management. Produces assigned work at high quality and according to timelines. Assists in the timely distribution of safety reports to Health Authorities, clients and client partners, in the appropriate format. | 11/25/2020 |
| 9691 | 10X Genomics Plesanton, CA Research Associate 2 - Molecular Biology/Product Development MS in Molecular Bio, Biochemistry, Genetics, Microbiology, Analytical Chemistry or Related Exp: 1+ Years |
This is a unique cross-disciplinary position that will work closely with a variety of groups including Molecular Biology, Chemistry, Microfluidics, QC, and Manufacturing, to develop and validate novel reagents for the rapid expansion of 10x product lines. Candidates must have a broad working knowledge of molecular biology and be able to apply that knowledge creatively and independently in a fast-paced work environment. The successful applicant will have exceptional attention to detail and the ability to meticulously execute and analyze highly complex experiments. Previous industry experience is essential. | 11/25/2020 |
| 9692 | 10X Genomics Plesanton, CA Process Engineer - MES MS in Statistics, Process Chemistry, Chemical or Manufacturing Engineering or Related Exp: 1-3 Years |
10x is looking for an outstanding Process Engineer to join the Process Development team. This is a key position for the commercialization of consumable products associated with Next Generation Sequencing chemistries. This person will be responsible for developing and integrating process control and yield optimization solutions for complex reagent manufacturing workflows and identifying process to function relationships. The ideal candidate will have a strong background in statistics and data analysis. Knowledge and hands on experience with trend analysis, yield enhancement methods, correlation and ANOVA analysis, quality systems databases, developing statistical process control for reagent manufacturing and previous experience in manufacturing SPC are required. | 11/25/2020 |
| 9693 | 1910 Genetics Cambridge, MA Research Associate - Biology BS/MS in Biology, Cell Biology, Molecular Biology, Biochemistry, Pharmacology, or Equivalent Exp: 0-3 Years |
Responsibilities: Executing high throughput screening (HTS) assays in strict accordance with the NIH NCATS Assay Guidance Manual. Developing and validating HTS biochemical assays for characterizing the activity and selectivity of potential drug candidates. Developing and validating HTS cell-based assays for characterizing the activity, selectivity, and cellular permeability of potential drug candidates. Performing a wide variety of experiments across molecular biology, cell biology, biochemistry, in vitro pharmacology, and in vivo pharmacology. Rigorously documenting all experimental procedures, data, results, manuals, etc. in an electronic laboratory notebook (eLN). Leveraging internal and external personnel to troubleshoot experiments. Effectively communicating research results both verbally and orally. Managing all external CRO relationships and cross-checking externally generated results with internal references and/or expectations. Managing all aspects of lab operations such as ordering, organizing, and restocking reagents, equipment, and other supplies. | 11/25/2020 |
| 9694 | Sinclair Research Auxvasse, MO Histology Technician BS with focus on lab processing Exp: n/a |
In this role, you will prepare histologic samples for evaluation in a pre-clinical research setting. It will be your job to not only prepare slides but monitor instrumentation and maintain laboratory supplies and cleanliness according to regulations. Throughout the day, you may check-in histology samples, trim tissues and prepare slides, or perform staining and microtomy. You will also assist in developing and implementing new processes while training research staff proper collection procedures. Strong leadership, organizational and analytical reasoning skills are a necessity. ASCP HT or HTL Certification is strongly preferred. | 11/17/2020 |
| 9695 | Sinclair Research Auxvasse, MO Study Coordinator BS in related field Exp: n/a |
The ideal candidate will have experience in animal handling and basic research techniques such as sample collection and data recording. As a Study Coordinator, you will help in all these areas, as well as overseeing the daily data collection and study conduct of our animal technicians and junior veterinary staff. It will be your responsibility to ensure they have a clear understanding of study protocol and activities. You will assist in planning out the study timeline, ordering supplies, developing forms, and managing pre-study meetings under the direction of a Study Director. You will be in a strategic role helping not only oversee studies for senior research staff, but communicating with our clients, other departments, and helping teach our animal technicians proper procedure and study conduct. | 11/17/2020 |
| 9696 | Singota Solutions Bloomington , IN Production Operator BS Engineering or Science Exp: n/a |
Production operators actively participate in all the manufacturing operations for the company including sampling/dispensing, drug product formulation, aseptic filling, finished dose labeling/kitting/packaging, and packaging component inspection (PCI). Responsibilities: Installing machine change parts and load recipes on fill machine. Staging/loading of components and preparation of fill path. Performing cleaning and VPHP decontamination of isolators. Assisting with environmental monitoring. Assist in process investigations, writing of deviations, and implementation of CAPAs to continuously improve operations. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes and procedures. | 11/17/2020 |
| 9697 | MicroVention Terumo Aliso Viejo, CA Engineer I/II (EIT) BS in Mechanical, Biomedical, Electrical, or Industrial Engineering, or Chemistry or Related Discipline Exp: 0-2 Years |
The Engineer I/II (EIT) supports development of medical device products with work including writing or verifying specifications, designing new products, fixtures, test processes, equipment and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Typical job duties might include developing new product concepts and products, engineering design and process development, generating intellectual property and writing invention disclosures, supervising assemblers, technicians, and specialists, and largely self-directed, capable of meeting project goals with moderate supervision. This 24-month rotational program is designed to train new Engineers on various aspects of MicroVention - Terumo technology, procedures, and processes. | 11/17/2020 |
| 9698 | Akorn Pharmaceuticals Somerset, NJ Aseptic Core Monitor Scientific degree preferred, microbiology Exp: 1 year |
Under the general supervision of the Supervisor, Aseptic Core Monitoring, the Aseptic Core Monitor oversees all activities in the aseptic environment to ensure continual compliance with cGMP and provides mentoring on aseptic technique for all aseptic personnel. This position requires expertise in all aspects of product manufacturing, ability to work hands on, strong leadership skills, and the ability to collaborate in a cross-functional environment. The individual will work closely with all departments in the aseptic manufacturing environment. Responsibilities: Complete daily visual audits of Aseptic Behavior inside the core during setup, formulation, fills, and sanitization processes. Navigate, Manage, and Mitigate Aseptic Risk. Partner with all cross functional groups to make recommendations for enhancements to aseptic process. Complete regular inspections of the physical conditions of the aseptic core including but not limited to floors, ceilings, doors, and walls. | 11/17/2020 |
| 9699 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I (Upstream) BS in Life Sciences, Chemistry, or Chemical Engineering Exp: 1-3 Years |
Sorrento is currently seeking a Manufacturing Associate who will be responsible for performing Upstream manufacturing tasks including tracking and control of raw material inventory; maintenance and operation of equipment in cGMP facilities; preparation of buffer and media; and assistance in operation of single use bioreactors for production of clinical and commercial products. Responsibilities: control and track raw material inventory, maintain and clean cleanroom facility and equipment, perform daily monitoring of equipment and assist Facilities and Engineering personnel as necessary on equipment maintenance and calibration, prepare media and buffer solutions, maintain cell culture flasks using good aseptic technique, assist in the operation of Single-Use Bioreactors, including the Wave Cellbag bioreactors and HyPerforma 100L, 500L, and 2000L systems. | 11/17/2020 |
| 9700 | Sorrento Therapeutics San Diego, CA Manufacturing Associate II (Downstream) BS in Life Sciences, Chemistry, or Chemical Engineering Exp: 1-3 Years |
Sorrento is currently seeking a Manufacturing Associate II responsible for performing downstream manufacturing tasks including tracking and control of raw material inventory, maintenance and operation of equipment in cGMP facilities, buffer preparation, assisting in setup and operation of purification equipment for production of clinical and commercial products. Responsibilities: assist in setup and operation of the filtration systems (depth filtration, sterile filtration, viral filtration, and UF/DF) including aseptic technique, review and revise cGMP Batch Production Records, SOP’s, protocols, and reports, provide support to cross-functional teams to meet production or timeline demands, demonstrate understanding in technical operations, safety, and Good Manufacturing Practices, and ensure the completeness and accuracy of manufacturing documentation per approved procedures. | 11/17/2020 |
| 9701 | Sorrento Therapeutics San Diego, CA QA Specialist AA/BS in Life Sciences, Chemistry, Biology, or Microbiology Preferred Exp: 1-2 Years |
The QA Specialist’s responsibilities are divided into three primary functional areas: Raw Material Inspection and Release, Label Generation, and Document Control. Raw Material Inspection: Associate is responsible for inspecting in-coming raw materials, releasing raw materials, obtaining and submitting test samples to the appropriate contract laboratory, and coordination of receipt of test results. Label Generation: Associate is responsible for ordering label and ribbon stock, generating Master Label templates from approved label specifications, producing labels for specific product lots, ensuring labels are verified as correct and are released in time to meeting the manufacturing schedule. Document Control: Associate is responsible for document control system, including but not limited to change control, word processing, training and equipment database, and maintenance of documents and document site; in addition, the associate shall assist with investigations as directed by QA Management; assist in the execution of validations, or other duties assigned by the head of QA. | 11/17/2020 |
| 9702 | Sorrento Therapeutics San Diego, CA Quality Control Microbiology Associate BS in Microbiology Exp: 1-2 Years |
This individual will contribute to providing microbiological support and testing of cGMP environments, as well as contribute to in-process, drug substance, and drug release testing. Responsibilities: Environmental monitoring of cGMP cleanrooms per FDA and USP guidelines, sampling of utilities (i.e. water, clean compressed air), input and manage environmental data, conduct QC testing of raw materials and utility samples; QC tests include, but not limited to bioburden, endotoxin, total organic carbon, conductivity, osmolality, and pH, initiate and participate in environmental excursions and OOS investigations and assess potential impact on product, maintain the QC Microbiology laboratory including ordering materials, inventory control and general lab housekeeping while sustaining safety standards, assist in qualification of test methods, equipment, and processes. | 11/17/2020 |
| 9703 | Sorrento Therapeutics San Diego, CA Research Associate BS/MS in Biology, Biochemistry, Chemical Biology, or Related Exp: Seniors/Recent Graduates will be considered |
Responsibilities: execution of cell-based assays to support characterization and development of lead candidates, aid in mechanistic and target validation studies using ELISA, SDS-PAGE, Western Blot, and flow cytometry, maintaining various cell lines for cell-based assays, assist in mAb/conjugate purification and buffer exchange, partake in instruments’ maintenance and calibration, lab cleanliness and orderliness, as well as ordering and replenishing stocks, analyze data and interpret results, keep clear and accurate records for both laboratory notebook and reports. | 11/17/2020 |
| 9704 | Sorrento Therapeutics San Diego, CA Research Associate I/II BS in Life Sciences Exp: 1+ Years |
The Oncolytic Immunotherapy group is seeking a highly motivated Research Associate to support the scientific goals of the research group by providing molecular biology, cell biology and virology support for oncolytic virus research and production. The candidate will also assist in the organizational aspects of the research group, such as spreadsheet and database maintenance. Responsibilities: assist in the cloning and screening of plasmid expression constructs for oncolytic virus development, assist in the molecular characterization of oncolytic virus candidates, including DNA and protein purification, PCR, sequencing analysis, and various protein expression analyses, perform maintenance of mammalian cell lines for virus production and characterization, perform standard virology procedures, including infections, plaque assays, and virus purification. | 11/17/2020 |
| 9705 | Sorrento Therapeutics San Diego, CA Upstream Process Development and Manufacturing Associate BS in Life Sciences, Chemistry, or Chemical Engineering Exp: 1-3 Years |
The Upstream Antibody Process Development & Manufacturing team is currently seeking an Upstream Associate who will be responsible for performing Upstream process development and manufacturing tasks including cell culture, cell banking, media preparation, benchtop bioreactor operation, and assistance in single use bioreactors operation for production of clinical and commercial products. Responsibilities: assist in the operation of Single-Use Bioreactors, including the Wave Cellbag bioreactors and HyPerforma 100L, 500L, and 2000L systems, review and revise current Good Manufacturing Practice (cGMP), Batch Production Records, SOPs, protocols, and reports, provide support to cross-functional teams to meet production or timeline demands, demonstrate understanding in technical operations, safety, and cGMP, ensure the completeness and accuracy of manufacturing documentation per approved procedures. | 11/17/2020 |
| 9706 | Solarea Bio Cambridge, MA Discovery Lab Research Associate BS/MS in Life Sciences related discipline Exp: 0-2 Years |
Solera Bio is seeking a Research Associate with experience working with bacteria and/or fungi with proficiency in aseptic technique, media and buffer preparation, culture inoculation and culture maintenance. The position will be a supporting role for the Discovery Lab with a large focus on culturing of microbes and the identification and quality control of bacterial and fungal strains. Responsibilities: perform culturing of bacterial and fungal strains as well as analytics such as quantifying cell numbers via cell counter, OD600, CFUs, propagate new cultures from parent stocks and perform quality control measures on new stocks/cultures via light microscopy, purity streaking, PCR, DNA extraction and Sanger Sequencing, assist in the manufacturing of microbial biomass for pre-clinical studies, assist in maintenance of routine lab operations through washing of glassware, autoclaving of media, glassware, and lab consumables, ordering and restocking of laboratory supplies, etc., write detailed electronic lab notebook (ELN) entries, analyze and present data in cross-functional team meetings. | 11/17/2020 |
| 9707 | Spark Therapeutics Philadelphia, PA Sample Management Associate BS Exp: 0-2 Years |
The Sample/Reagent Technician will perform a variety of sample management tasks including receiving, labeling, transferring, tracking, location management, distribution, archival activities, shipping and disposal of biological samples and reagents. These activities include samples of both clinical and non-clinical origin. These activities will be managed using Laboratory Information Management System (LIMS). Reporting to the Sample Management Lead, this position is accountable for the timely maintenance of an accurate biological and reagent inventory required to support activities for all Research, Clinical and Process Development groups. These activities include working with lab personnel to review sample paperwork against samples to ensure accuracy; communication of discrepancies to appropriate personnel and assistance with problem solving; strict adherence to all procedural SOPs effecting sample handling, storage and documentation; communication of confirmed sample receipts to appropriate internal and external parties; entry and accuracy of all sample information within the LIMS sample tracking systems; distribution of biological samples, sample information and paperwork to scientific staff. | 11/17/2020 |
| 9708 | Spark Therapeutics Philadelphia, PA Process Engineer BS/MS Chemical or Biochemical Engineering or related Exp: 1+ Years |
Responsibilities: Provide direction on the Facility and Process Requirements (Both Upstream and Downstream) for new and existing facilities. Be the key point of contact between engineering design firms and internal Spark Manufacturing and MS&T resources. Evaluate conceptual aspects of technical process designs to ensure sound decisions and investments are made in accordance with business strategy and internal policy/governance and assess new innovative technologies. Develop relationships with Roche Engineering resources and leverage existing facility and process designs, requirements documentation, and equipment vendor relationships and other design documentation from Roche. Ensure plans are created and updated in a timely manner, communicated to relevant stakeholders, assess risks, and manage deliverables. Meet scheduled milestones to ensure project/program objectives are met in a timely manner. Use rapid design principles in accordance to Corporate Standards. | 11/17/2020 |
| 9709 | Spark Therapeutics Philadelphia, PA Manufacturing Science and Technology Downstream Process Scientist/Engineer BS in Biochemistry or Engineering Field Exp: 0-2 Years |
The Manufacturing Science and Technology (MST) Downstream Process Scientist/Engineer is an entry-level position within the MST Lab team, which is responsible for carrying out laboratory experiments to support clinical and commercial manufacturing of gene therapy products and late-stage process development activities. To support manufacturing, the incumbent will develop an understanding of Spark manufacturing processes in order to assist in the evaluation of raw materials and equipment, investigation of process deviations and development of process improvements. Late-stage process development activities, such as process characterization, will require the incumbent to build an understanding of new processes in the clinical pipeline delivered from the Process Development organization, with whom the incumbent will interact with regularly. The incumbent’s major responsibility in the activities described above is hands-on execution of bioprocessing laboratory experiments for downstream unit operations, such as tangential flow filtration, preparative chromatography and dead-end filtration. The experimental scope spans experimental design, in-lab execution, documentation of results using Good Documentation Practices and data analysis. | 11/17/2020 |
| 9710 | Spark Therapeutics Philadelphia, PA Manufacturing Science and Technology Upstream Process Scientist/Engineer BS in Biochemistry or Engineering Field Exp: 0-2 Years |
The Manufacturing Science and Technology (MST) Upstream Process Scientist/Engineer is an entry-level position within the MST Lab team, which is responsible for carrying out laboratory experiments to support clinical and commercial manufacturing of gene therapy products and late-stage process development activities. To support manufacturing, the incumbent will develop an understanding of Spark manufacturing processes in order to assist in the evaluation of raw materials and equipment, investigation of process deviations and development of process improvements. Late-stage process development activities, such as process characterization, will require the incumbent to build an understanding of new processes in the clinical pipeline delivered from the Process Development organization, with whom the incumbent will interact with regularly. The incumbent’s major responsibility in the activities described above is hands-on execution of laboratory experiments for upstream bioprocessing, such as cell culture in flasks and bioreactors. The experimental scope spans experimental design, in-lab execution, documentation of results using Good Documentation Practices and data analysis. The incumbent will also take part in the tech transfer of production processes into clinical and commercial manufacturing suites through interaction with the Process Development organization and both internal and external manufacturing partners. | 11/17/2020 |
| 9711 | Spark Therapeutics Philadelphia, PA Quality Assurance Specialist/GCP BS/MS in Life Sciences related discipline Exp: 1+ Years |
This is an entry level role that will be responsible for supporting administrative and operational GCP and GVP audit and compliance activities under guidance and supervision of the Clinical Quality Assurance GCP Lead (and/or designee). This role is meant to prepare/ train an individual to take on a CQA auditor role. Responsibilities: Work with CQA Management to develop CQA business reports, as applicable, support CQA auditors, as needed (i.e. preparation, conduct, follow-up), support CAPA activities, support the development, maintenance, and/or continuous improvement of Global CQA Quality System (SOPs, work instructions, tools, templates, etc.), support applicable Clinical Development, Pharmacovigilance and non-clinical SOP development, training and administration, support the development and tracking of compliance metrics. | 11/17/2020 |
| 9712 | SQZ Biotech Watertown, MA Research Associate, Immunology BS/MS in Relevant Field Exp: 0-2 Years/0-1 Years |
This role supports the execution and analysis of experiments and data through technical execution and by supporting experiment planning and organization. This role meticulously documents experiments and their outcomes which helps support potential regulatory filings. Responsibilities: Meticulously execute bench work, analyze data, troubleshoot, and communicate findings; perform in vitro assays using multi-color flow cytometry, ELISA/ELISPOT, and cellular biology methods as well as in vivo studies using murine disease models; optimization of new assays with minimal oversight and analysis of data; gather and critically analyze and experimental data to shape decisions around the direction of studies; deliver biomolecules to cells using the SQZ device; support quality control and review of Investigational New Drug (IND) filings and packages; manage large data sets and compiling data for analysis; contribute to experimental design and project direction in support of team goals. | 11/17/2020 |
| 9713 | SQZ Biotech Watertown, MA Research Associate, Immunology (Tolerance) BS/MS in Relevant Field Exp: 0-2 Years/0-1 Years |
SQZ Biotechnologies is looking for a highly motivated, collaborative, and dynamic Senior Research Associate for our Immune Tolerance team within the Exploratory Department. This role is an opportunity to focus on developing novel antigen-specific tolerance therapies for autoimmune diseases and gene therapies. The scope of this work will encompass planning and execution of in vivo and in vitro experiments for various research projects. This position requires effective collaboration within the Tolerance team and regular presentation of scientific results. Responsibilities: perform in vivo studies using murine disease models; deliver biomolecules to cells using the SQZ device; perform in vitro assays using multi-color flow cytometry, ELISA/ELISPOT, and cellular biology methods; execute bench work, analyze data, troubleshoot, and communicate findings; procure, organize, and maintain inventory of materials needed for experiments; contribute to the collective success of the Tolerance team. | 11/17/2020 |
| 9714 | SQZ Biotech Watertown, MA Senior Research Associate, Immunology MS in Relevant Field Exp: 1+ Years |
This position works closely with a scientist to design and execute experiments aimed at pre-clinical validation of new cancer treatments. Responsibilities: perform in vivo studies using murine disease models; bench work, analyze data, troubleshoot, and communicate findings; perform in vitro assays using multi-color flow cytometry, ELISA/ELISPOT, and cellular biology methods; optimization of new assays; manage large data sets and help with data visualization; work split between solo and team work, executing on multiple projects simultaneously; possess excellent organizational skills and “can-do” attitude and ability to shift focus based on multiple priorities and deadlines. | 11/17/2020 |
| 9715 | SQZ Biotech Watertown, MA Senior Research Associate, Infectious Diseases MS in Relevant Field Exp: 1+ Years |
The Research Associate supports the execution and analysis of experiments and data through technical execution and by supporting experiment planning and organization for multiple projects. Responsibilities: perform in vitro assays using multi-color flow cytometry, ELISA/ELISPOT, and cellular biology methods; gather and critically analyze and experimental data to shape decisions around the direction of studies; procure, organize, and maintain inventory of materials needed for experiments; design, execute and troubleshoot experiments with minimal supervision; contribute to experimental design and project direction in support of team goals; maintain a lab notebook and contribute to supporting documentation when necessary; work with skilled teams in a fast-paced, collaborative, and technical research environment; work independently and execute on multiple projects simultaneously, considering cross-functional projects. | 11/17/2020 |
| 9716 | SQZ Biotech Watertown, MA Associate Engineer, Process Development BS in Chemical Engineering, Bioengineering, or related Exp: 0-6 Months |
The candidate will support process development efforts for our clinical and pipeline cell therapy products. Responsibilities: Perform hands-on laboratory work using SQZ proprietary equipment and data analysis; maintain electronic lab notebook, study plans, and experiment reports; support across different functional teams to ensure successful completion of necessary studies; support troubleshooting and identification of corrective actions during the execution of laboratory experiments; adhere to safe laboratory practices; prepare experimental summary presentations to process development team and management; perform data analysis and statistical trending on in-house lab experiments. | 11/17/2020 |
| 9717 | SQZ Biotech Watertown, MA Engineer, Process Development BS/MS in Chemical Engineering, Bioengineering, or related Exp: 1+ Years/0-1+ Years |
SQZ Biotech is seeking a highly-motivated Engineer to join their Process Development team. The successful candidate will support process development efforts for our clinical and pipeline cell therapy products. This role will have high cross-functional visibility across the organization. Responsibilities: perform hands-on laboratory work using SQZ proprietary equipment and data analysis; maintain electronic lab notebook, study plans, and experiment reports; collaborate across different functional teams to ensure successful completion of necessary studies; support troubleshooting and identification of corrective actions during the execution of laboratory experiments; participate as person in plant (PIP) for clinical manufacturing; adhere to safe laboratory practices; prepare experimental summary presentations to process development team and management; perform data analysis and statistical trending on in-house lab experiments. | 11/17/2020 |
| 9718 | Sunrise Pharma Rahway, NJ Regulatory Affairs Associate MS Pharmaceutical Manufacturing, Pharmacy, Regulatory Affairs, or related Exp: 6+ Months |
Responsibilities include creating & implementing labels for OTC & ANDA submissions, assisting in ANDA submissions using eCTD submission software, preparing & maintaining annual reports, SOP, deviations & OOS reports, and reviewing product complaints & queries & support in developing regulatory strategies & launch OTC products. | 11/17/2020 |
| 9719 | Sunrise Pharma Rahway, NJ Production Supervisor BS in related field Exp: n/a |
Responsibilities include production planning, reviewing batch records, maintaining appropriate records/reports, providing training to production/packaging personnel; overseeing production technicians and providing technical assistance when needed, such as maintenance and programming of production machinery; writing validation protocol and equipment performance qualification protocols and writing standard operating procedures for production and manufacturing areas. | 11/17/2020 |
| 9720 | Synthorx La Jolla, CA Research Associate II MS in Biomedical Sciences or related field Exp: n/a |
Responsibilities: Performs protein titer determination of fermentation pellets and in-process samples using HPLC and mass spectrometry. Executes SEC, IEX and RP-purity assays following SOPs for product characterization. Performs protein and peptide detection assays using qualitative and quantitative techniques including UV/Vis, SDS-PAGE, and western blot. Assists in troubleshooting and maintaining modern analytical instrumentation. Executes experiments, conducts analysis and reports results. Maintains Standard Operation Protocols (SOPs) and reference materials. Manage and maintain required reagents, laboratory environment, and equipment needed to carry out assignments. Assists research team in protein and peptide purification and prepares samples for mass spectrometry analysis. Prepares research reports and presentations for team meetings. Works closely with team leaders to complete highest priority work to reach goals and milestones. | 11/17/2020 |
| 9721 | Talaris Therapeutics Louisville, KY Cell Processing Associate I, Manufacturing Operations BS in related field Exp: 6+ Months |
A Cell Processing Associate I, to be based in Louisville, KY is a production professional responsible for the day-to-day operations related to clinical cell therapy manufacturing in a GMP and GTP compliant ISO 7 classified cleanroom facility. The primary responsibilities of this role focus on cell processing; strong aseptic techniques; adherence to SOPs and cGMP regulations and accurate competition of documentation associated with clinical manufacturing, ability to work in a cleanroom environment (ISO 8, 7, 5); and ability to use manufacturing and cryopreservation equipment, including routine cleaning and maintenance. Secondary responsibilities include development and programmatic organization activities. | 11/17/2020 |
| 9722 | T-Cure Bioscience Sherman Oaks, CA Senior Research Associate MS in Life Sciences, Preferred emphasis in Cellular Molecular Biology Exp: n/a |
The Research Associate will assist Senior Scientist with DNA and RNA preparation, molecular cloning, transfection and transduction of human cell lines and retrovirus/lentivirus production. T-Cure provides a competitive salary and excellent benefits and exposure and experience in the growing field of immune-oncology. Responsibilities: effectively communicate with the leadership team, Senior Scientists and fellow researchers for collaborative projects and laboratory duties; participate in laboratory meetings and Journal Clubs and present data displaying the progression of projects and future directions; work with both limited supervision and as a team member; learn new techniques and assays to drive project progression; maintain a laboratory notebook with working knowledge of Good Laboratory Practices (GLPs). | 11/17/2020 |
| 9723 | TherapyX Advanced Protein Therapeutics Louisville, KY Project Manager/Executive Assistant MS in Biological Sciences, Biostatistics, or related Exp: 1+ Years |
The candidate will support senior management in enabling all facets of drug and vaccine development, including data management and analysis, as well as the creation of documentation supporting regulatory submissions, applications and final reports. The candidate will also possess the ability to work within a fast-paced multidisciplinary environment to drive the development, implementation and maintenance of software and hardware tools to support and track multiple projects simultaneously. Responsibilities: Work with research and development scientists, in-house, as well as with representatives of diverse CROs and other service providers in multifaceted support of drug and vaccine development; this will include quality control and analysis of internal and external data sets, generation of reports, regulatory documents, etc., as well as the creation and operation of related software and hardware tools. Work closely with in-house and outsourced expertise to add statistical rigor and quality control to analyses and provide concise summaries of key experiments. Bring strong attention to detail to the team along with skills / aptitudes in developing data processing, analysis and communication tools. | 11/17/2020 |
| 9724 | Turning Point Therapeutics San Diego, CA Clinical Trial Associate BS or equivalent in scientific or health care field Exp: 1-3 Years |
Turning Point Therapeutics is seeking a highly motivated individual to join the company as a Clinical Trial Associate (CTA) within the Clinical Operations Team, reporting into the Director of Clinical Operations. The Clinical Trial Associate is responsible for the oversight and management of clinical operations activities or projects. The CTA will interact with Clinical Operations teams and collaborate effectively with CROs, vendors and clinical trial sites. The CTA supports the timely conduct of clinical studies according to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and all applicable regulations governing the conduct of clinical trials. Responsibilities: Support all aspects of Turning Point Therapeutics’ clinical trials from initiation, planning, execution, maintenance and close-out. Collaborate/Interact with CROs, vendors and clinical study sites. Support patient enrollment and data collection are completed in accordance with study timelines and objectives. Review and assess study documents required for site activation and investigational product release. Review Site selection/Visit reports: Qualification Visits, Initiation Visit Reports and Interim Monitoring Visit Reports on an ongoing basis. | 11/18/2020 |
| 9725 | Translate Bio Lexington , MA Research Associate I/II, Formulation Stability BS/MS in Chemistry, Physical Chemistry, Chemical Engineering or Biochemistry Exp: 0-2 Years |
Translate Bio is seeking a highly motivated and scientifically rigorous individual to join the Delivery and Formulation Development team as a Research Associate. The position will focus on stability evaluation of frozen and lyophilized drug products. Responsibilities: Conduct experiments for advancing understanding of stability of lipid nanoparticles (LNP) drug products and provide storage and shipping conditions aligned with success administration of drug product for preclinical and clinical studies. Perform experiments to establish stability parameters, improving physical and chemical stability and integrity of drug product upon long term storage. Support drafting new and revising existing stability protocols for long term stability of drug product. Contribute in writing/reviewing analytical method protocols/stability protocols. Prepare technical reports and presentations for clear communication of scientific findings across interdisciplinary teams. | 11/18/2020 |
| 9726 | Translate Bio Lexington , MA Research Associate I/II, Delivery Formulations BS/MS in Chemistry, Physical Chemistry, Chemical Engineering or Biochemistry Exp: 0-4 Years |
Translate Bio is seeking a highly motivated and scientifically rigorous individual to join the Delivery Formulations team as Research Associate I/II. The position will focus on developing novel lipid nanoparticle (LNP) formulations for mRNA delivery for the development of vaccines. Responsibilities: Prepare formulations and perform characterization assays /data analysis with focus on in vivo studies, drug carrier design/development, assay development etc. Support formulation development activities related to increasing stability and formulation optimization. Contribute in writing/reviewing analytical method protocols & stability protocols. Prepare technical reports and presentations for clear communication of scientific findings across interdisciplinary teams. | 11/18/2020 |
| 9727 | Translate Bio Lexington , MA Associate Scientist/Senior Research Associate, Plasmid Engineering MS in Chemistry, Physical Chemistry, Chemical Engineering or Biochemistry Exp: 1-3 Years |
Translate Bio is seeking a highly motivated and scientifically rigorous candidate to lead from the bench as an Associate Scientist/Senior Research Associate in the RNA Sciences Team. The position will focus on plasmid synthesis, DNA characterization and supporting the Translate Bio programs and collaborations. The position will be highly collaborative and give the successful candidate a broad range of experience across functions within the organization. Responsibilities: Synthesis, purification, and characterization of plasmid DNA. Support high throughput plasmid synthesis and purification efforts. Support platform projects by performing assays including capillary & gel electrophoresis. Independently design and execute decision-quality research. Prepare technical reports, presentations, and recommendations to management and other stakeholders. | 11/18/2020 |
| 9728 | Translate Bio Lexington , MA Associate Engineer, Process Development BS/MS in Chemical Engineering/Biochemistry or a related field Exp: 1-2 Years |
Translate Bio is looking for a highly motivated and scientifically rigorous individual to join the Process Development team as an Associate Engineer. The position will focus on optimization and scale-up of Lipid Nanoparticle (LNP) formulations in support of all vaccine related programs at Translate Bio. Responsibilities: Assist with optimization and scale-up of Bulk Drug Product (BDP) formulation and Final Drug Product (FDP) processes encompassing a wide range of different drug substances and multi-component LNPs. Assist with design and implementation of stability studies focused on identification of formulation conditions resulting in long term stability at multiple storage temperatures. Perform routine and complex analytical methods for characterization of LNP drug products with minimal supervision. Keep detailed records and present study results to R&D and CMC teams as needed. Critical thinking and analysis of data will be central to all aspects of this position. Assist with preparation of technical reports and presentations to clearly communicate scientific findings as needed. | 11/18/2020 |
| 9729 | Translate Bio Lexington , MA Associate Engineer, GMP Process Development BS/MS in Chemical Engineering or related field, MS preferred Exp: 1-2 Years |
The Associate Engineer reports to the Senior Engineer and is an integral part of CPD&P team. This position offers opportunities to focus on drug substance and drug product process development, manufacturing, regulatory and analytical support, validation, and data review for drug substances and drug products. The Associate Engineer is responsible for assisting in the development and execution of scalable and robust processes for drug substance and drug product. This position will assist the CPD&P Subject Matter Expert (SME) for process knowledge transfer for drug substance and drug product to support cGMP manufacturing. | 11/18/2020 |
| 9730 | Translate Bio Lexington , MA Associate Scientist, Analytical CMC MS in Analytical Chemistry or Biochemistry Exp: 0-2 Years |
The Associate Scientist, Analytical CMC contributes to the analytical development function within CMC and overall CMC strategy of drug development at Translate Bio. The scientist supports the development, validation and transfer of analytical methodologies for incoming raw materials, starting materials, drug substance, and stability testing. The scientist has expertise in biologics, biochemistry, synthetic intermediates, and analytical chemistry. Responsibilities: Help manage analytical chemistry activities both internally and at external contract laboratories for critical raw materials and starting materials. Guide CRO to design and perform phase-appropriate method development, testing, and validation. Manage product stability study programs, trending data. Demonstrate extensive knowledge in state-of-the-art analytical technologies. Authorize/review analytical method development reports, validation protocols/reports, instructions/SOP’s for relevant analytical functions. | 11/18/2020 |
| 9731 | Trevigen Wallingford , CT Quality Technician BS in Scientific Field Exp: 0-2 Years |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including hands-on evaluation of microfluidic cartridge products. Responsibilities: Adherence to safety procedures and compliance with department specific SOP’s. Understanding of quality body of knowledge, standard laboratory procedures, and record keeping guidelines. | 11/18/2020 |
| 9732 | Trevigen Minneapolis, MN Integration Process Engineer BS Science Related Degree Exp: 0+ Years |
This position is a >75% computer-based position that will focus on the integration of our existing and new product lines into our manufacturing systems (primarily AX). This position will involve taking existing manufacturing documents and processes and enabling them to be integrated and managed in AX, ICA, etc. Projects will be diverse, with primary focus being on established existing product lines, but will also include product lines currently managed outside of AX, ICA or involve the integration of newly acquired product lines from the growing family of Bio-techne brands. Integration of these processes will enable better planning, resource management, reproducibility, reduce back-order times, improve documentation and will facilitate inter-departmental transfers and new product release. This position will also be responsible for assisting the rest of the Process Engineering team as an AX expert and resource during investigation of post-launch manufacturing, QC, marketing, and customer issues. This position will also enable optimization of processes to enhance or improve robust manufacturing of products manufactured at the Minneapolis site. | 11/18/2020 |
| 9733 | Trevigen Woburn, , MA Research Associate BS in Biology, Biochemistry, Molecular Biology, Immunology, or related Exp: 0-2 Years |
This hands-on position will support development and troubleshooting of novel polymeric reagents for cell activation, cell separation and other CGT applications. As part of the R&D team, this role will support product development by formulating reagents and testing them in a variety of analytical and cell-based assays. The role will work closely with product teams to develop new products and troubleshoot production of existing products for research and clinical applications. Responsibilities: Characterize hydrogel microparticles via ELISA, microscopy and flow cytometry based assays using established protocols in support of product development and manufacturing efforts. Generate test batches of proprietary hydrogel microparticles using laboratory equipment and functionalize product prototypes with proteins using bioconjugation protocols. Conduct cell-based experiments to evaluate functionality of product prototypes on immune cells. With supervision design, execute and interpret experiments to meet R&D objectives. Collaborate with a diverse team of biologist, chemists and engineers to develop new products for cell and gene therapy applications. | 11/18/2020 |
| 9734 | PAR Pharmaceutical Rochester, MI Process Engineer I MS in chemical or other engineering Exp: 1+ year(s) |
The Process Engineer I, with guidance, performs various duties related to optimization and analysis of production processes, new products, processes and technology transfers. Prepare and execute engineering study protocols, manufacturing and packaging experimental / feasibility study / validation batch records and protocols and complete interim and / or final summary reports for marketed and new products. Perform or assist on-site and site-change technical transfer, scale-up or scale-down factor evaluation, manufacturing / packaging process and equipment troubleshooting, and SOP preparation and review. Process Engineering duties within a single location. Make decisions within guidelines and policies. Follow established procedures to perform assignments, with general instructions on the process and desired outcome. Work is reviewed for soundness of technical judgment and accuracy. etc. | 11/9/2020 |
| 9735 | PAR Pharmaceutical Chestnut Ridge, NY Manufacturing Operator l HS diploma or equivalent Exp: 0-2 years |
The Manufacturing Operator I performs functions relating to the processing of drug products, ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements and in conjunction with all Standard Operating Procedures (SOPs). Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. Learns to apply skills and knowledge to recognize issues and to increase efficiency, throughput and quality. Learns, understands and runs processes to meet the assigned standards/routers and fulfills the assigned schedule; when these are not achieved, may participate in the debrief to understand the reasons why and what needs to be corrected moving forward. Assists in troubleshooting process issues. Responsible for the safe and efficient execution of job duties. etc. | 11/9/2020 |
| 9736 | Paragon Genomics Hayward, CA Quality Assurance Specialist BS in molecular biology, chemistry, or other life science Exp: 1+ year(s) |
Paragon Genomics is a fast-growing life sciences company developing advanced reagents and assay kits for next-generation sequencing (NGS). We are seeking a Quality Assurance (QA) Specialist that can help us transition our Quality Management System (QMS) from ISO 9001 to ISO 13485 certification. The QA Specialist ensures compliance with policies and procedures, serves as the main point of contact for customer quality audits and provides quality system performance reports to management. This position will be expected to take a hands-on approach to activities in production and other processes, in order to identify and recommend opportunities for improvement. The QA Specialist will report to the CEO. etc. | 11/9/2020 |
| 9737 | Paragon Genomics Hayward, CA Research Associate-R&D BS in biology, molecular biology, chemistry, or related Exp: 0-1+ year(s) |
We are seeking a Research Associate in Molecular Biology to play an important role in the development of novel NGS target enrichment assay technologies and support current operations. This is a laboratory-based position with great career potential for a junior scientist or prospective scientist who already has or wishes to gain hands-on molecular biology experience in the next-generation sequencing space. The candidate should have good interpersonal and problem-solving skills. He/she should be driven to learn and motivated to develop great products. The ideal candidate thrives in a fast-paced and multi-disciplinary environment. This position will report to the Molecular Biology Scientist. etc. | 11/9/2020 |
| 9738 | ThermoFisher Scientific Princeton, NJ Scientist II, Process Development MS in biology, chemistry, chemical engineering, or related Exp: Not necessary for MS candidates |
Acts as a key scientist in the upstream process development group within the BioProcess Sciences division of the Pharma Services Group. This position will be responsible for the execution of and hands on support of projects such as the development and characterization of mammalian cell lines for the clinical/ commercial manufacture of recombinant protein products. Participates in the execution of projects developing mammalian cell culture processes to support the production and manufacturing of recombinant proteins (including mAbs) with activities including: Clone and media/feed screening using AMBR technology. Bioreactor culture development including fed-batch (2 to 250L scale) with both glass and single use cell culture technologies. etc. | 11/9/2020 |
| 9739 | ThermoFisher Scientific Cincinnati, OH Operator II, Manufacturing HS diploma or equivalent Exp: 1-2 year(s) |
Operators in this position utilize equipment, procedures, and Line Packaging Records (LPR’s) to package batches of product on one or more packaging lines. The Packaging Operator can operate equipment, recognize and remedy quality problems, and perform changeovers and cleanups as required. Perform packaging line operation, including operating/monitoring equipment, inspection, hand cartoning or packing, labeling, palletizing, cleanup, hopper filling, and other duties as required. Assist in Line Clearances between batches, follow cleanup sheet directions, follow verbal orders or requests from group leader/supervisor, and perform other duties as required. Good manual dexterity and fine motor skills needed to carry out the physical aspects of the job. Job requires lifting of materials weighing up to 35 pounds for periods of time. etc. | 11/9/2020 |
| 9740 | ThermoFisher Scientific Alachua, FL Associate I, MFG Upstream AS/BS in a related science or engineering field Exp: 1-3 year(s) |
This position entails routine hands-on bioprocess manufacturing within a cGMP cleanroom commensurate with the individual’s level of technical expertise, training, and qualification strictly following defined procedures. What will you do? Perform upstream bioprocess manufacturing in a GMP cleanroom involving adherent and suspension cell culturing while following detailed protocols, PBRs and SOPs. Conduct routine suite cleans, preparation and/or request necessary components and raw materials, labels, etc. to successfully execute production batch records. Adhere to all cGMP procedures and safety/quality standards. Maintain a culture of safety and compliance to all environmental health and safety protocols. etc. | 11/9/2020 |
| 9741 | ThermoFisher Scientific San Diego, CA Clinical Research Associate II, In vitro diagnostics BS in a scientific discipline Exp: 0-1 year(s) |
The primary role of this position is targeted toward clinical studies support and study site management. In this role the primary responsibilities include: Coordinating and conducting activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Ensuring studies are conducted and documented in accordance with the study protocol, standard operating procedures, good clinical practices and other applicable regulatory requirements. Collect all clinical study essential documents. Participate in lab assessment visits. Ensure that CRO activities and timelines are in coordination with project requirements. Coordinate internal and external clinical studies preparation and planning. Implement and document communication with CRO and laboratories to ensure project progress. etc. | 11/9/2020 |
| 9742 | ThermoFisher Scientific Pleasanton, CA Material Handler HS diploma or equivalent Exp: 1 year |
Essential Functions: Receive materials and/or finished goods on a daily basis. Verify the quality, type and amount of materials received are correct and that the appropriate documentation is present (e.g. packing list). Examine, sort, arrange, count, store, pick, and pack items for storage and/or shipment in accordance with established procedures and customer requirements. Prepare routine documentation. Operate material handling equipment (e.g. hand truck, pallet jack, dock lever, etc.). Follow warehouse safety standards and use of proper PPE (Personal Protective Equipment). Prepare and ship materials and/or finished goods in a timely manner according to customer requirements. etc. | 11/9/2020 |
| 9743 | ThermoFisher Scientific St. Louis, MO Biopharmaceutical Technician I - Days AS/BS in biology, biochemistry, or chemistry Exp: 0-3 years |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. etc. | 11/9/2020 |
| 9744 | ThermoFisher Scientific Logan, UT BioCenter Assembly Specialist 1 - Second Shift HS diploma or equivalent Exp: 1-2 year(s) |
Responsible for the manufacturing, assembly, and/or packaging of BioProcess Containers in a clean room environment. Technicians carry out the production process by closely following the SOP (Standard Operating Procedures), WID (Work Instruction Documents) and blueprints or drawings as they relate to assembly, materials handling, equipment operation, and finished goods packaging. This position requires following cGMP (Current Good Manufacturing Practices) and working in a fast paced team environment. Key Responsibilities: (Include but are not limited to the following) Follow all safety requirements and cGMP (Current Good Manufacturing Practices) requirements. Follow work instruction document, standard operating procedures and standard works. Assembling product using specific written instructions, blueprints and drawings. etc. | 11/9/2020 |
| 9745 | PBL Assay Science Piscataway, NJ Assay Services Scientist I/II/III BS in the life sciences Exp: 1+ year(s) |
The Assay Services Scientist I / II / III works primarily with cell culture-based bioassays, executing antiviral bioassays, ELISAs and other highly sensitive immunoassays for characterizing proteins and reagents; analyzing data and drafting client reports; and developing new and custom assays to support the growth of the Assay Services Group. ESSENTIAL DUTIES AND RESPONSIBILITIES: Execute immunoassays on ELISA, and other highly sensitive platforms like Electrochemiluminescence (MSD), Single Molecule Array (Simoa), and Single Molecule Counting (Erenna). Execute antiviral and antiproliferative cell-based bioassays. Analyze data and write client reports. etc. | 11/9/2020 |
| 9746 | PBL Assay Science Piscataway, NJ Quality Control Scientist I BS in the biological sciences Exp: 1-2 year(s) |
To ensure the quality of PBL reagents the Quality Control (QC) Scientist I will perform release and stability testing of interferons, antibodies, and manufactured ELISA kits. In addition, the QC Scientist I will perform bioassays or immunoassays to troubleshoot relevant customer issues and design and initiate experiments and projects to improve the quality of PBL products. The QC Scientist I may also serve as back up to the Product Development, Assay Services, or Manufacturing departments as needed: such additional duties may include designing and performing ELISA testing protocols, custom bioassays, and solution preparation. This individual will be involved with document control, SOP writing, and recordkeeping. etc. | 11/9/2020 |
| 9747 | PBL Assay Science Piscataway, NJ R&D Scientist I MS Exp: 0-2+ years |
The R&D Scientist is responsible for the hands-on development of immunoassays, such as ELISAs and cell-based assays, for commercial production. This individual plans and executes design, development, and Manufacturing transfer of bioanalytical assays for product commercialization. The R&D Scientist is also responsible for development of custom assays and reagents for clients. ESSENTIAL DUTIES AND RESPONSIBILITIES: Develops immunoassays and cell-based assays for commercial markets. Executes assay performance verification in multiple biological matrices from normal and diseased organisms. Ensures robustness and ruggedness of assay performance to facilitate ease of large-scale manufacture. etc. | 11/9/2020 |
| 9748 | PBL Assay Science Piscataway, NJ Senior Protein Scientist BS/MS in the biological sciences Exp: 1-4+ year(s) |
The Senior Scientist develops and executes purification schemes for new product candidates, develops analytical methods for protein characterization, and enhances current purification procedures with the goal of increasing yield, purity and activity. The Senior Scientist is also responsible for development of custom reagents and assays for clients. ESSENTIAL DUTIES AND RESPONSIBILITIES: Expression, purification, and characterization of recombinant proteins from mammalian and bacterial cell sources. Develops new reagents, such as antibodies or purified proteins, for immunoassay use. Develops and implements new assay methods and technologies for protein characterization. Facilitates the transfer and troubleshooting of new products to the Manufacturing department. etc. | 11/9/2020 |
| 9749 | Perrigo Georgia, VT Chemistry Analyst (Tues-Sat 4 PM-12:30 AM) BS in chemistry or related Exp: 1-2 year(s) |
The incumbent performs a variety of standard analyses on raw material, in-process, and finished product samples using chemical analysis techniques, according to compendia (i.e. USP, FCC, or AOAC) or Perrigo methodologies. Performs routine analyses of raw material and finished product samples as assigned, demonstrates proficiency in 5 – 10 separate Analytical Methods (AM’s). Analytical instrumentation used in this group is primarily NMR Fat Analyzer, Nitrogen Analyzer, NIR Spectroscopy, and HPLC (High Pressure Liquid Chromatography). etc. | 11/9/2020 |
| 9750 | Perrigo Grand Rapids, MI Laboratory Technician (Part-Time) - Oral Care Business Unit [Ranir] BS in chemistry, biology, engineering, or related Exp: 1+ year(s) |
Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. RESPONSIBILITIES: Coordinate with internal team to conduct general laboratory work, including liquid formulation batching, wet chemistry and instrumental analysis using specialized lab equipment. Maintain accurate and complete records of testing results and report results to manufacturing and engineering teams. Prioritize workload and departmental needs to a test schedule to meet individual and company deadlines. Maintain all laboratory equipment according to GMP, GLP, and 5S standard; ensure lab meets organization needs for accurate and sustainable test practices. etc. | 11/9/2020 |
| 9751 | Perrigo Covington, OH QC Chemist - 1st Shift, 2/2/3 Schedule BS in chemistry, food science, or biology Exp: 1-2 year(s) |
We are currently looking for a highly motivated QC Chemist who will work 1st shift on a rotating 2/2/3 schedule. Description: Collect samples including raw material, finished product, process equipment and environmental. Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations. Operate laboratory equipment. Participate in internal and external quality audits. Maintain personal laboratory work area and assist with general laboratory cleaning. etc. | 11/9/2020 |
| 9752 | FCX Performance Carleton, MI Valve Technician HS diploma/AS/AA Exp: 1-3 year(s) |
Essential Functions & Responsibilities: Repair relief valves, control valves, on/off valves and pneumatic actuators in FCX actuation facility or customer plant locations. Mechanically and electrically troubleshoot, inspect, and test valves at specified job worksites. Primary worksites include FCX valve repair centers with occasional customer in-field work sites. Perform pre-testing, disassembly, cleaning, in process inspection, machining, lapping, painting, assembly, testing, and final inspection on various types of valves and actuation. Perform testing on certified test equipment, and complete all documentation by working under a QA / QC / National Board VR program. Complete field service worksheets and submit to job coordinator upon completion of work. Understanding of pneumatic and digital controls. Ability and knowledge to reference appropriate valve manuals for repair requirements. etc. | 11/10/2020 |
| 9753 | FCX Performance Lexington, MA Pipette Calibration Technician - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Pipette Technicians are expected to take a proactive role in supporting the Pipette Services Team and in providing client pipette support. The Pipette Technician is expected to build a high level of trust with internal and client personnel. This trust is developed through consistently upholding PCI Values and demonstrating Honesty, Integrity, Pride, Accountability, Teamwork, and Commitment. Responsibilities/ Assignments: Pipette Calibration Technician I. Works with basic laboratory instrumentation, as well as operates computer-based applications utilized in a laboratory environment. Further develops technical skill whenever possible through internal or external training programs. Completes calibrations, qualifications, PMs and changes with GxP documentation in an accurate and timely manner and in accordance with PCI and Client Standard Operating Procedures (SOPs). etc. | 11/10/2020 |
| 9754 | FCX Performance San Francisco, CA Calibration Technician I - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Completes calibrations and qualifications in a safe, timely, and accurate manner, following PCI and client specific policies and proposals. Responsible for proper handling and maintenance of PCI and client equipment, including testing and standards equipment. Identifies project supply and equipment needs and conveys to the appropriate resource to ensure availability. Works to understand client needs and requirements through effective communication and develops client relationships through excellent customer service. Ensures client requests are conveyed to the appropriate PCI management resource and met in accordance with management direction. etc. | 11/10/2020 |
| 9755 | FCX Performance Appleton, WI Valve Technician HS diploma or equivalent Exp: 1-3 year(s) |
FCX Performance is an Applied Industrial Technologies Company and a leading process flow control company. As a Valve Technician you will be responsible for assembling control valves, on/off valves and pneumatic actuators in our FCX actuation facility. Essential Functions & Responsibilities: Mechanically and electrically troubleshoot, inspect, and test valve assemblies. Understanding of pneumatic and digital controls. Ability and knowledge to reference appropriate valve manuals. Exhibit an ability to effectively communicate with plant personnel regarding valve and instrumentation equipment and customer requirements. Obtain all site specific and safety related training. Assist others as required. Job duties are subject to change as directed by management. etc. | 11/10/2020 |
| 9756 | FCX Performance Boulder, CO Calibration Technician I - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Completes calibrations and qualifications in a safe, timely, and accurate manner, following PCI and client specific policies and proposals. Responsible for proper handling and maintenance of PCI and client equipment, including testing and standards equipment. Identifies project supply and equipment needs and conveys to the appropriate resource to ensure availability. Works to understand client needs and requirements through effective communication and develops client relationships through excellent customer service. Ensures client requests are conveyed to the appropriate PCI management resource and met in accordance with management direction. etc. | 11/10/2020 |
| 9757 | FCX Performance Waltham, MA Calibration Technician I - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Completes calibrations and qualifications in a safe, timely, and accurate manner, following PCI and client specific policies and proposals. Responsible for proper handling and maintenance of PCI and client equipment, including testing and standards equipment. Identifies project supply and equipment needs and conveys to the appropriate resource to ensure availability. Works to understand client needs and requirements through effective communication and develops client relationships through excellent customer service. Ensures client requests are conveyed to the appropriate PCI management resource and met in accordance with management direction. etc. | 11/10/2020 |
| 9758 | FCX Performance Raleigh, NC Pipette Technician - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Pipette Technicians are expected to take a proactive role in supporting the Pipette Services Team and in providing client pipette support. The Pipette Technician is expected to build a high level of trust with internal and client personnel. This trust is developed through consistently upholding PCI Values and demonstrating Honesty, Integrity, Pride, Accountability, Teamwork, and Commitment. Responsibilities/ Assignments: Works with basic laboratory instrumentation, as well as operates computer-based applications utilized in a laboratory environment. Further develops technical skill whenever possible through internal or external training programs. Completes calibrations, qualifications, PMs and changes with GxP documentation in an accurate and timely manner and in accordance with PCI and Client Standard Operating Procedures (SOPs). Always considers safety when executing tasks and projects. Ensures that PCI work areas are safe, neatly organized and professional on-site and in office. etc. | 11/10/2020 |
| 9759 | Pharmaron Germantown, MD Associate Bioanalytical Scientist, Accelerator Mass Spectrometry BS/MS Exp: 0-1+ year(s) |
This position is responsible for carrying out sample analysis and data processing within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company policies. Contributes to the laboratory and equipment maintenance to ensure efficient operations. Essential Functions: Participate in day-to-day operation of the Laboratory, the analysis of samples and associated duties. Responsible for handling and processing of biological samples including competent handling and pipetting technique. Prepare/review data tables and reports within Laboratory Information Management System (LIMS). Ensure adequate levels of reference materials, control matrix, and project-specific consumables and resources are available to meet the objectives of the study. Prepare/review forms and SOPs. Assist in training personnel in the operation and maintenance of laboratory equipment. Assist in data processing, QC checking and data compilation. etc. | 11/10/2020 |
| 9760 | Pharmaron Germantown, MD Laboratory Technician, Accelerator Mass Spectrometry (Germantown, MD) BS/BA Exp: 6-12 months |
We are looking for a Laboratory Technician to work on a full-time basis in our Germantown, MD facility. This position is responsible for carrying out sample analysis and data processing within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company Policies. Contributes to the laboratory and equipment maintenance to ensure efficient operations. Essential Functions: To work to the Company’s quality procedures in accordance with GLP and GCP regulations and be involved in working to and generating a culture of continuous improvement. To comply with the Company’s Health and Safety, MOSH and ionizing radiation procedures. To participate in the day‐to‐day operation of the Laboratory, the analysis of samples and associated duties. To prepare, with other staff, Standard Operating Procedures (SOPs) and other generic documents (eg worksheets and spreadsheets) as required. To purchase chemicals and other laboratory supplies, gaining financial approval as appropriate. etc. | 11/10/2020 |
| 9761 | Phibro Animal Health Corporation Sarasota, FL Fermentation Technician - Tech II HS diploma or equivalent Exp: 1-3 year(s) |
Osprey Biotechnics is a worldwide leader in the development of bioproducts for a large range of bioremediation and bioaugmentation applications including wastewater, soil/ground water, industrial and consumer products, poultry, and agriculture. We are seeking enthusiastic, team-oriented individuals to join our fermentation group in this full-time position. This position is 1st shift, Monday through Friday from 5:00am - 1:30pm, with some weekend work and OT potential. Key Responsibilities: Understand and perform sterilizing and aseptic technique. Assembly and disassembly of valves, equipment, and fermentation tanks. Ability to assemble and inoculate a tank. etc. | 11/10/2020 |
| 9762 | Phibro Animal Health Corporation Sarasota, FL Spray Dry Technician I HS diploma or equivalent Exp: 1-3 year(s) |
Osprey Biotechnics is a worldwide leader in the development of bioproducts for a large range of bioremediation and bioaugmentation applications including wastewater, soil/ground water, industrial and consumer products, poultry, and agriculture. We are seeking enthusiastic, team-oriented individuals to join our down-stream processing group in this full-time, entry-level position. This position is 2nd shift, Monday through Friday from 12pm - 8:30pm, with some weekend work and OT potential. Key Responsibilities: Retrieving materials to spray dry. Operating spray drier and monitoring its automated operation. Recording temperature readings throughout the operation and verifying the chart recording. etc. | 11/10/2020 |
| 9763 | Phibro Animal Health Corporation Sarasota, FL Fermentation Technician - Tech I HS diploma or equivalent Exp: 1-3 year(s) |
Osprey Biotechnics is a worldwide leader in the development of bioproducts for a large range of bioremediation and bioaugmentation applications including wastewater, soil/ground water, industrial and consumer products, poultry, and agriculture. We are seeking enthusiastic, team-oriented individuals to join our fermentation group in this full-time, entry-level position. This position is 1st shift, Monday through Friday from 5:00am - 1:30pm, with some weekend work and OT potential. Operation, care and routine maintenance of production scale fermentation and culture processing equipment. Assembly and disassembly of valves, equipment, and fermentation tanks. Cleaning and sanitization of valves, equipment, and fermentation tanks. etc. | 11/10/2020 |
| 9764 | Phibro Animal Health Corporation Sarasota, FL Blending Technician HS diploma or equivalent Exp: 1-3 year(s) |
Osprey Biotechnics is a worldwide leader in the development of bioproducts for a large range of bioremediation and bioaugmentation applications including wastewater, soil/ground water, industrial and consumer products, poultry, and agriculture. We are seeking enthusiastic, team-oriented individuals to join our blending department in this full-time, entry-level position. This position is 1st shift, Monday through Friday from 7:00am - 3:30pm, with occasional weekend work and OT potential. Key Responsibilities: Able to perform repetitive blending and line bottling operations. Stand for long periods of time. Basic arithmetic skills such as adding, subtracting, and measuring volume/weight. etc. | 11/10/2020 |
| 9765 | Poseida Therapeutics San Diego, CA Research Associate - Immuno-Oncology MS in immunology, molecular biology, or related Exp: 0+ years |
Poseida is seeking an outstanding candidate to join our immuno-oncology team. The Research Associate will support the development of chimeric antigen receptor (CAR-T) cellular therapies against cancer and will be involved in bench work, laboratory studies, and the coordination of research projects with the assistance of a senior lab member and/or lab director. Responsibilities: These may include but are not limited to: Support preclinical development of CAR-T cellular therapies. Studies may include work with molecular cloning, tissue culture, cell isolation from blood products, virus production, and cell separation. etc. | 11/10/2020 |
| 9766 | Precision BioSciences Durham, NC Research Associate I/II, CMC Analytical BS in the biological sciences Exp: 1+ year(s) |
The Research Associate I or II, CMC-Analytical – Cell Biology, will work in the Cell Therapy Bioassay/Immunoassay/Flow Cytometry group of Precision BioSciences. This individual will provide biologic analytical support for Product Sciences and Cell Therapy Process Development projects. The position will contribute to development efforts for CART-cell projects by providing sample preparation and analysis in a timely manner. This position is lab-based and will share facilities and resources with the Cell Therapy teams. Primary responsibilities will include: Design, development, characterization and documentation of analytical methods for the phenotypic characterization of genome-edited cell therapy products. etc. | 11/11/2020 |
| 9767 | Precision Medicine Group Norton, MA Biorepository Technician BS in biology, chemistry, or other life science Exp: 0-2 years |
Our Biorepository Technicians assist in shipment and receipt, the retrieval preservation of biological samples that arrive daily or are stored in the repository. Essential duties include but are not limited to: Unpack specimens and record all pertinent information in Incoming Shipment Batch and Incoming folder. Distribute confirmation of shipment receipt form if required by project. Check information on sample vial against information provided by the study site or data coordinating center. Scan samples into data management system, BSI. Ensure paperwork is accurate and inform Supervisor/Manager of any discrepancies. etc. | 11/11/2020 |
| 9768 | Precision Medicine Group Chicago, IL Business Intelligence Analyst I - Pharma Analytics BS/BA Exp: 1-3 year(s) |
Business Intelligence Analysts (BIA I & II) play a meaningful role in achieving our team’s goal of exceeding customers’ expectations with leading edge data management and data-driven insights and applications. A Glimpse of What Your Day-to-day will look like: Design, develop and administer a system for self and others to evaluate appropriateness of data for analytic hypotheses and applications. Develop and direct a process to clean and integrate complex healthcare datasets in order to create the data foundation for further analytics, client applications, and the development of key client insights. Contribute client team meetings for client engagements and strategic projects requiring complex data management support. etc. | 11/11/2020 |
| 9769 | Precision Medicine Group Norton, MA Clinical Operations Assistant HS diploma or equivalent Exp: 0-1 year(s) |
The Intern/Clinical Operations Assistant will be assigned tasks to assist in the daily operations of the Clinical Affairs department. This position will aid in ensuring a functional, clean work environment and will be responsible for supporting ongoing projects. Essential functions of the job include but are not limited to: Complete directed tasks as specified by Clinical Project Managers. Complete directed tasks as specified by the Data Management team. Appropriate handling of whole blood. Observe PBMC isolation and cryopreservation. Maintain a clean workspace. etc. | 11/11/2020 |
| 9770 | Precision Medicine Group Frederick, MD Kit Production Technician HS diploma or equivalent Exp: 1-2 year(s) |
Prepare and ship the important materials used in sample collection to meet our client’s specifications. Essential duties include but are not limited to: Kit Manufacturing: Prepare Sample Collection Kits per Standard Operating Procedures and Project Operating Procedures. Assemble and label Kit Components; including collection tubes, vials, documentation, and boxes per specific Assembly Instructions. Aliquot reagents using Aseptic Technique. Complete Batch Records and supporting documentation. etc. | 11/11/2020 |
| 9771 | Precision Medicine Group Frederick, MD Processing Technician AS/BS in biology, chemistry, or other life science Exp: 1-2 year(s) |
This role is responsible for receiving, accessioning, and processing patient samples. In addition to processing blood and leukopaks for our Accucell line of cryopreserved cells. Essential duties include but are not limited to: Process and cryo-preserve fresh biological samples: Receive and inventory all incoming fresh biological samples into electronic LIMS database. Perform cell isolations and/or separate whole blood and body fluids into various components. Perform cryopreservation of all isolated cells. Prepare all reagents used in lab. etc. | 11/11/2020 |
| 9772 | Precision Medicine Group Philadelphia, PA Remote - Statistical Programmer I - Clinical Trial Services BS in statistics, mathematics, computer science, or related Exp: Entry level |
What to expect day to day: Create specifications for derived/analysis datasets. Program analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. Generate SDTM domains, ADaM datasets, and Define.xml files. Provide programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests. Perform quality control for SAS programs and other study documents (e.g., presentations and reports). Document the quality control review process. Review output across programs to ensure consistency. etc. | 11/11/2020 |
| 9773 | Precision Medicine Group Redwood City, CA Research Assistant - Fresh Biological Samples BS in biology, chemistry, or other life science Exp: 1-2 year(s) |
In this role: You will process fresh patient specimens and nonclinical samples. You will perform PMBC or cell subset isolations, plasma fractionations, serum separations, cell thawing, cell counting and generating whole blood aliquots. You will receive and process nonclinical samples such as whole blood units and/or leukopaks. etc. | 11/11/2020 |
| 9774 | Poseida Therapeutics San Diego, CA Research Associate - Immuno-Oncology BS/MS in Immunology, Oncolocy, or Related Exp: 0-3 Years |
Poseida is seeking an outstanding candidate to join the immuno-oncology team. The Research Associate will support the development of chimeric antigen receptor (CAR-T) cellular therapies against cancer and will be involved in bench work, laboratory studies, and the coordination of research projects with the assistance of a senior lab member and/or lab director. Responsibilities: Support preclinical development of CAR-T cellular therapies. Studies may include work with molecular cloning, tissue culture, cell isolation from blood products, virus production, and cell separation. Plan and execute flow cytometry based assays for characterization of cellular products and analysis of tissue samples from animal studies. Plan and execute in vitro cell based immunoassays to functionally characterize CAR-T product. | 11/5/2020 |
| 9775 | Poseida Therapeutics San Diego, CA Manufacturing Associate BS in Chemistry or Engineering Exp: 0+ Years |
The Manufacturing Associate is part of the Poseida internal manufacturing team in support of Poseida’s clinical production of cell therapies. This position will support front line non-viral cell therapy GMP production activities, process transfers, and technology improvements towards the successful delivery of released product to meet the needs of Poseida’s clinical trials. Responsibilities: Perform critical GMP aseptic operations in ISO 5 and ISO 7 production environments, following paper-based and/or electronic batch records, standard operating procedures (SOPs), policies, and work instructions to ensure safe and compliant operations. Assist with startup activities of a new cGMP facility by collaborating with PD, MSAT, Facilities, and Quality departments. | 11/5/2020 |
| 9776 | Poseida Therapeutics San Diego, CA Lab Technician BS Exp: 6+ Months |
Poseida is seeking an outstanding candidate to join the Research Operations team. The Lab Technician is responsible for providing broad support for research personnel by maintaining lab facilities, carrying out basic lab equipment maintenance, washing and autoclaving glassware, coordinate collection of biohazard/chemical waste, and replenishing lab supplies. Responsibilities: Set up and carry out daily operational maintenance of lab equipment. Coordinate routine equipment maintenance and preventative maintenance with various vendors. Provide immediate support and troubleshoot issues that arise in the labs (freezer leaks, centrifuge malfunction, incubator contamination, etc.). Conduct daily lab inspections to look for equipment issues (alarms, leaking freezers, etc.), help create a safe lab work environment, and communicate safety violations or issues encountered to Research Operations team. | 11/5/2020 |
| 9777 | PRA Health Sciences Salt Lake City, UT Quality Control Associate HS Diploma Exp: 1-2 Years |
The Quality Control Associate will support the preparation and conduct of studies by monitoring and reviewing study data, by a review of data entry and/or by QC of completed source documents. Responsibilities: May assist in the identification of data entry errors through data entry reconciliation. QC completed source documents. Fully document all completed QC on appropriate forms. Participates in internal team meetings when requested. Ensures all identified errors are resolved in a timely manner. May identify trends in documentation errors by item or staff member. May assist with developing new work methods for data entry and QC of study documentation. Review and QC source documents with the eCRF or draft database as requested | 11/5/2020 |
| 9778 | PRA Health Sciences Blue Bell, PA Clinical Trial Assistant BS Highly Preferred Exp: 0-2 Years |
You will be responsible for setting up, tracking and maintaining Clinical Site related documents. You will help manage and review regulatory documents as well as maintain the Local Study File. Assist with coordinating the distribution, retrieval and review of regulatory documents required for the initiation of the Clinical Study, through maintenance, and close-out. Performs the role of Clinical Trial Assistant (CTA) supporting the Local Trial Manager and Site Manager to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution and closing of clinical trials. Performs regulatory document review and approval, including site specific Informed Consents. Ensures trial related activities are in compliance with GCO SOPs, policies and local regulatory requirements. May contribute to process improvement, training and mentoring of other CTA’s. | 11/5/2020 |
| 9779 | PRA Health Sciences Boston, MA Clinical Trial Coordinator - Training BS or Higher Exp: 1-4 Years |
The CTC is a detail oriented profession, who supports the Clinical Quality Management department in areas of process, training and compliance, SUSAR distribution, and ensuring that studies are inspection ready. Responsibilities: Distributes SUSAR reports to investigators. Runs and distributes compliance reports. Assists in vendor oversight. Performs QC of documents and participates in revisions. Routes documentation for appropriate signage. Collects, organizes and prepares regulatory documentation for transfer to Trial Master File and assists with tracking of document under guidance. Helps to develop and maintain tracking tools for event investigation, training, SUSAR distribution and inspection readiness. Coordinates meetings, prepares agendas and takes minutes. Responsible for ongoing maintenance of the GCO component of learning portals. Produces metric reports for event investigations | 11/5/2020 |
| 9780 | Precision Biosciences Durham, NC Research Associate I/II CMC Analytical BS/BA Exp: 1+ Years |
The Research Associate I or II, CMC-Analytical – Cell Biology, will work in the Cell Therapy Bioassay/Immunoassay/Flow Cytometry group of Precision BioSciences. This individual will provide biologic analytical support for Product Sciences and Cell Therapy Process Development projects. The position will contribute to development efforts for CART-cell projects by providing sample preparation and analysis in a timely manner. This position is lab-based and will share facilities and resources with the Cell Therapy teams. Primary responsibilities: Design, development, characterization and documentation of analytical methods for the phenotypic characterization of genome-edited cell therapy products using multi-color flow cytometry, immunoassay and bioassay. | 11/5/2020 |
| 9781 | MacroGenics Rockville, MD QA Document Control Specialist I HS Diploma or Equivalent Exp: 1+ Years |
The QA Document Control Specialist I/II is responsible for executing key document control-related activities that support various departments at MacroGenics. This position is responsible for scanning and performing quality checks of GMP documents. The individual will also provide coverage in the document archive room and assist with organizing, retrieving, and filing GxP documents. The individual must possess the ability to handle multiple priorities, be able to interface and communicate effectively with individuals from various departments daily and be able to work as part of a team. Responsibilities: Scanning batch records, test data, protocols, reports, and placing them into their respective electronic folders daily. Routing, reviewing, and overall management of GxP documents in MasterControl, including SOPs, forms, specifications, and protocols. Conducting quality control reviews of scanned documents for accuracy and completeness daily. | 11/5/2020 |
| 9782 | MacroGenics Rockville, MD Bioprocess Associate II MS Biochem/Chem/Life Sciences Exp: 0+ Years |
The Bioprocess Associate II is responsible for all aspects of cell culture process development and validation as well as technology transfer, including process optimization, scale-up, characterization and validation studies, toxicology material production, process transfer to manufacturing, and production support. This individual will also be responsible for analyzing and summarizing the data in technical reports and presentations and troubleshooting as needed. Responsibilities: Design and execute experiments, including shake flasks, production bioreactors, and harvest operations, to support the development of biologics products. Complete documentation to support testing procedures including data capture, forms, logbooks, and inventory batch records. Analyze experimental data for process understanding and further improvements, draw conclusions and interpret results using statistical tools, including media and process development, process characterization and validation. Contribute to authoring of protocols, operating procedures and technical reports ensuring timely and accurate completion. | 11/5/2020 |
| 9783 | RedShiftBio Burlington, MA Mechanical Engineer BS/MS Mechanical Engineering Exp: 0+ Years |
RedShift BioAnalytics is seeking a Mechanical Engineer to support the development of analytical instrumentation for the characterization of biologic drugs. The position is both exciting and challenging, with exposure to automation, microfluidics, thermal management, and opto-mechanics in addition to instrumentation design. | 11/5/2020 |
| 9784 | Refuge Biotechnologies Menlo Park, CA Senior Reseaarch Associate BS/MS Immunology/Cell Biology Exp: 1-2 Years |
In this role, you will contribute to the company’s efforts to develop next-generation cell therapies in solid tumor malignancies. Specifically, you will be part of a preclinical development team focused on engineering approaches to enhance CAR T anti-tumor activity. The successful candidate will have a strong immunology background and will be expected to work in a collaborative cross-functional team environment, perform experiments, organize and analyze results, communicate effectively and present findings in team meetings. Responsibilities: Employ viral-based strategies for the genetic modification of T cells with chimeric antigen receptors (CARs). Culture and characterize CAR T cells. Plan and execute in vitro functional assays with human T cells according to project timelines and goals. Assist with design of murine models/experiments to evaluate CAR T cell function in vivo. | 11/5/2020 |
| 9785 | REGENEXBIO Rockville, MD Validation Engineer BS/MS Engineering or Related Exp: 1+ Years |
You will be responsible for all aspects of qualifying GxP systems including, but not limited to, GxP analytical equipment, controlled temperature units, GMP manufacturing equipment, and GxP computer systems. In addition, you will maintain up-to-date knowledge of validation requirements, practices, and procedures and coordinate with others participating in validation activities. Responsibilities: Develop, collaborate on, and review validation deliverables for equipment and computer systems used in GxP laboratories and manufacturing. Interact with other departments and vendors to facilitate validation deliverable preparation and execution. Write and execute validation protocols in accordance with SOPs and industry standards. Assist with troubleshooting and investigations of validated systems. Conduct periodic reviews and requalifications of systems to ensure they are maintained in a validated state. | 11/5/2020 |
| 9786 | REGENEXBIO Rockville, MD Associate Scientist, Bioanalytical Sciences BS/MS Exp: 1-2 Years |
As the Associate Scientist/Senior Associate Scientist of the Bioanalytical Sciences team, you will be responsible for developing and validating bioanalytical methods to support our gene therapy products pipeline. You will have the opportunity to collaborate with many different groups across the organization, including Research and Early Development, Quality, and Clinical Development and may oversee Contract Research Organizations to ensure that all applicable bioanalytical test methods are appropriate for the stage of non-clinical and/or clinical development. Responsibilities: Develop, qualify and/or validate robust bioanalytical methods (ligand binding and/or cell-based assays) to support the Company pipeline. Troubleshoot and resolve analytical method and instrument issues to successful resolution. Keep detailed, accurate testing records and assure that laboratory equipment is calibrated, standardized, and monitored, as appropriate. Author technical documents (analytical method qualification/validation/transfer documents, technical reports, SOPs, etc.). | 11/5/2020 |
| 9787 | REGENEXBIO Rockville, MD In-House CRA / Clinical Trial Associate BA/BS Exp: 1-2 Years |
As the In-house CRA you will support and coordinate the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs and acts as a pivotal point of contact for the clinical trial team. Under general supervision, you will assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. Responsibilities: Assists in the development and editing of study-related materials (e.g. consent forms, study binders, site study aids). Assists with preparation of training workshops, Investigator/Advisory Board meeting materials. Assists with all phases of clinical trial activities (e.g. start-up, conduct, and close-out). Develops study tracking tools (e.g. site lists, enrollment tracking, vendor spreadsheets) | 11/5/2020 |
| 9788 | Sanaria Rockville, MD Quality Control Associate BS Exp: 1-2 Years |
This position is responsible for performing routine release and stability testing of final product following cGMP regulations and Sanaria SOP. This position also requires performance of in vitro assay, Viability assay and other QC tests. Responsibilities: Processing and conducting immuno-assays on preclinical and clinical product. Generating and maintaining documentation as per Sanaria documentation procedure. Writing and executing new SOP and protocols. Using technical proficiency and independent thought to collaborate with others to implement new assays. Adhering to industry and government standards regarding aseptic technique and tissue culture practices. Maintaining lab materials inventory and equipment’s. | 11/5/2020 |
| 9789 | SCA Pharma Windsor, CT Lab Analyst - Microbiology BS Exp: 0-2 Years |
The Microbiology Laboratory Analyst is responsible for performing laboratory oversight of GMP compounding activities at SCA Pharmaceuticals. The Laboratory Analyst performs Lab investigations, OOL/OOS, executes CAPA's as they pertain to the Microbiology department and supports validation and technical change control activities. This position requires advanced understanding of site processes in order to write technical documents including engineering studies and standard operating procedures. The individual occupying it is expected to be capable of working with minimal supervision. The Laboratory Analyst is expected to communicate well with fellow employees as well as Compounding Operations and Quality Assurance departments. Responsibilities: Perform daily Bacterial Endotoxin testing on all batches/lots of product as part of release testing, and assist with Endotoxin product validation activities as necessary. Write technical documents for Microbiology Lab including standard operating procedures (SOP's), investigations, corrective and preventative action plans. | 11/5/2020 |
| 9790 | Scholar Rock Cambridge, MA Associate Scientist, Antibody Characterization BS/MS Molecular Biology/Biochem/Related Exp: 1-3 Years |
The Antibody Discovery & Engineering group at Scholar Rock is developing best-in-class antibody therapeutics to help patients with unmet medical needs. We are seeking an outstanding individual to support the discovery and characterization of antibodies to enable the lead selection for multiple therapeutic programs. The successful candidate will work with the phage display and hybridoma teams to establish and execute biophysical and bioanalytical assays for comprehensive characterization of antibodies. The person in this role will have the opportunity to learn various aspects of biotherapeutic drug development in a fast-paced matrixed environment. Responsibilities: Characterize the binding properties of antibodies by ELISA, flow cytometry, and kinetics tools. Perform stability and pre-formulation studies on antibodies to assess their “drug-like” qualities. Maintain detailed records of experimental protocols and data in laboratory notebooks in accordance with company policy. | 11/5/2020 |
| 9791 | Sebela Pharmaceuticals Holbrook, MA Analytical Services Scientist BS, MS Preferred Exp: 1-4 Years |
This is a Laboratory Bench Position for routine/non-routine testing and development/validation of new product testing. Responsibilities: Develop/Optimize/Validate analytical test methods and write protocols/technical reports/test methods in a cGMP environment to support R&D product pipeline requirements. Evaluation of contract laboratory test method validation reports for completeness and adherence to cGMP/USP standards. Perform non-routine evaluation and testing related to investigations and technology. Perform routine laboratory testing. Review analytical data for completeness, accuracy, and compliance. Provide training regarding test methods, equipment, and compliance. Other laboratory duties as assigned. | 11/13/2020 |
| 9792 | Sebela Pharmaceuticals Holbrook, MA QC Chemist BS in Chemistry or Related Discipline Exp: 0-2 Years |
This is a Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. Responsibilities: Perform testing of raw materials and products. Perform instrument qualification and maintenance. Perform test method validation/verification. Review analytical data for completeness, accuracy, and compliance. Perform training on procedures, equipment, or quality systems. Other duties as assigned. Individual contributor, but may be assigned as a project lead or trainer commensurate with experience or expertise | 11/13/2020 |
| 9793 | Seer Bio Redwood City, CA Formulations Research Associate BS/MS Chemistry or Materials Science Exp: 1 Year |
Seer’s new Formulations Research Associate will be responsible for fundamental laboratory organization activities, including inventory, stocking, and the cleaning of laboratory glassware. Responsibilities: Laboratory organization – stocking, inventory and cleaning of laboratory glassware. Support our characterization efforts and execute standard characterization protocols (DLS, XPS, TEM). Assist with materials synthesis, helping to set up reactions and purify synthesized materials. Implementing standard operating procedures for current materials. Effectively present data internally to other Seer scientists and technologists. Enable the efficient operation of our fast-paced laboratory. Execute standard SOPs reliably. Proficiency in sample prep methods for materials characterization. Work with the broader Formulations team in the development of cutting-edge materials. | 11/13/2020 |
| 9794 | Seer Bio Redwood City, CA Process Development Engineer BS/MS Chemical Engineering, Chemistry, Materials Science or Related Exp: 1Year |
Reporting to the Associate Director of Process Development, we are seeking an exceptional Engineer to join our team based in our Redwood City office. Experience synthesizing nanoparticles and scaling such complex processes is highly desired. The role requires skills including particle synthesis, surface modification, and incorporates both organic and inorganic chemistry. Seer’s new Engineer will be empowered to assist in the scale-up and manufacture of critical components of our platform. Responsibilities: Support lab activities for synthesizing and scaling nanoparticles and other biosensor samples. Maintain and operate laboratory equipment including balances, reactors, filtration equipment, and particle sizers. Support the company’s interactions with contract development and manufacturing organizations (CDMOs) to source and characterize nanoparticles. Organize, evaluate, and communicate data in an effective and scientific manner. | 11/13/2020 |
| 9795 | Nordson Brooklyn Park, MN Production Operator I HS diploma or equivalent Exp: No experience required |
Position Summary: Position consists of assembling and inspecting medical devices in a clean room environment while under general supervision in accordance with specific work instructions and SOPs. Assembly and inspection sometimes done under a microscope. This position requires the ability to work with small tools and assemble small components using a high degree of dexterity and accuracy. This position requires direct contact with an implantable medical device. Essential Job Duties and Responsibilities: Must be able to work under direct supervision and take work instruction from Supervisor and Leads, work cooperatively and productively within a team environment. Ability to do repetitive tasks, Detail-Oriented and adherence to Nordson’s Safety Policy. Read, Understand and follow Standard Operating Procedures without deviating from the outlined process after training has been completed. Ability to work on Development Department process steps with significant Technician oversight. etc. | 10/31/2020 |
| 9796 | Nordson Austintown, OH Material Handler HS diploma or equivalent Exp: 1-3 year(s) |
A material handler is responsible for sequencing all WIP, driven by dispatch scheduling, at each relevant machining center to enable work center efficiency and elevate execution of OTD to 90% or greater. Essential Job Duties and Responsibilities: Offloads incoming bar stock. Moves bar stock from storage area into the manufacturing process as required. Reviews machining center daily dispatch reports for machining centers and sequences bar stock in order at the relevant machining center. Transfers bar stock from machining center to machining center to assist operator efficiency. Removes clutter from the process line areas. Removes and disposes of dunnage properly. Empties machining chip hoppers as necessary. etc. | 10/31/2020 |
| 9797 | Nordson Brooklyn Park, MN Product Development Technician Supervisor - Nordson MEDICAL AS/AA/BS/BA Exp: 1-3 year(s) |
The Product Development Technician Supervisor is responsible for planning and directing daily activities, in coordination with the Development team, of personnel focused on Development assembly. The supervisor supports goals and objectives according to GMP’s, SOP’s and established policies, practices, procedures, quality, and cost standards. The role focuses on continuously improving efficiencies and working cross functionally to achieve overall company objectives. Essential Job Duties and Responsibilities: Participate in Development project planning to understand upcoming Development needs, changes in schedules, current challenges, and space/equipment allocation to help establish strategies to meet team goals. Act as a cross functional liaison for Development and Operations personnel resource communication and alignment. Manage personnel problems/concerns effectively and act as the primary point of contact for personnel feedback. etc. | 10/31/2020 |
| 9798 | Nordson East Providence, RI Machine Technician - 2nd shift HS diploma or equivalent Exp: 1-3 year(s) |
Machine Technician I is responsible for setting up and operating specialized automated production assembly equipment as well as setting up manual jigs and fixtures for secondary operations. Additionally, responsible for detailed record keeping for equipment and production related activities. Essential Job Duties and Responsibilities: Setup and operate automated production equipment. Setup manual jigs and fixtures for production operators. Provide training and instruction to operators on proper equipment operation. Prepare all materials in advance of setup. Record all materials used for each production order for lot number traceability. Monitor production and make adjustments to ensure quality at all times. Keep detailed records of adjustments made during production. etc. | 10/31/2020 |
| 9799 | Nordson Loveland, CO Assembly Technician HS diploma or equivalent Exp: 1 year |
Assemble finished goods according to work instructions while maintaining outlined quality procedures. Essential Job Duties and Responsibilities: Assemble finished goods according to work instructions. Sort defective parts as directed by quality control. Able to work in a clean room environment. De-gate parts as required. etc. | 10/31/2020 |
| 9800 | Nordson Salem, NH Pre Form Technician Second Shift Temp to Hire HS diploma or equivalent Exp: 1+ year(s) |
To utilize a wide range of equipment, fixtures, gages and hand tools to support the manufacturing of medical device products. To maintain all logs, forms and resulting paperwork. Essential Job Duties and Responsibilities: Understand the need to deliver quality product and demonstrate a commitment to quality. Contribute to continuous improvement and Lean initiatives. Follow clean room protocols for hygiene and gowning. Maintain regular attendance. Must be able to work flexible hours. Trained to all manual preform procedures. Trained to all machine preform procedures. Able to follow written and oral instructions well. etc. | 10/31/2020 |
| 9801 | Nordson Loveland, CO Product Equipment Technician HS diploma or equivalent Exp: 1-3 year(s) |
This position is primarily responsible for the set up, troubleshooting, and up-time of various automated and manual packaging equipment. The Product Equipment Technician (PET) works to develop and enhance the programs and setup on these machines to increase accuracy, efficiency, and throughput. The PET will also set up and program automated de-gating equipment used at the press during plastic injection molding operations, and will be instrumental in the development and refinement of programs and processes used by these robotic devices. The PET works daily in the company’s ERP system (IFS) to verify and enter data while ensuring the timely completion of all assignments. This position will ensure proper line clearance of all equipment prior to the start of any new Shop Order while ensuring all packaging equipment is properly set up to accurately and repeatedly produce the required bag sizes, labeling, and part count while validating that the bag appearance and its contents meet the quality expectations of Value Plastics, Inc. Furthermore, this position will serve as a back-up for other responsibilities such as visual AQL inspection and part cleaning operations. etc. | 10/31/2020 |
| 9802 | Alvogen Norwich, NY Process Engineer I BS/MS Exp: 0-3 years |
The Process Engineer I reports to the Director of Process Engineering and Technical Services (PETS). RESPONSIBILITIES: Support the development, transfer, and validation of manufacturing processes. Define transfer plan for internally and externally developed products. Utilize a risk based approach to define experimental/feasibility studies. Identify critical process parameters and their impact on product quality. Create and present technical presentations at project milestones. Perform process optimization. Develop and execute process validations. Provide technical support were needed. Administrative duties: Document preparation (plans, risk assessments, DOE, Batch records, protocols, summary reports, investigations, etc.…). Use statistical methods for data analysis. etc. | 10/31/2020 |
| 9803 | Nostrum Laboratories Kansas City, MO Packaging Technician HS diploma or equivalent Exp: 1 year |
The Packaging Technician performs routine packaging operations for the production of pharmaceutical products; operates packaging line equipment according to established SOPs and department procedures. Duties and Responsibilities: Prepares and cleans room, equipment, facility and documents for manufacturing and packaging process. Verifies calculations, process steps and yield. Ensures that processes, tools, products and materials meet established quality standards and requirements. Notifies management when inventory fails below certain levels. Assists in the assembly and disassembly of process equipment as necessary. Examines sample of finished product per batch record instructions for conformance with specifications. Notifies supervisor of manufacturing / packaging deviations and assists with proper resolution/documentation. etc. | 10/31/2020 |
| 9804 | Nova Biomedical Billerica, MA Manufacturing Engineer – Mechanical BS In mechanical, industrial, manufacturing, or electrical engineering Exp: 1-3 year(s) |
START YOUR APPLICATION: Sanvita Medical Corporation, an exciting new medical device company in diabetes healthcare operating within one of Nova Biomedical’s facilities, is hiring a Manufacturing Engineer to provide technical support for a new line of medical devices. Working in a small and highly driven team, you will have an opportunity to learn and grow, while contributing to a wide range of projects and assignments, including: Update and create all forms of manufacturing documentation conform to Quality System Regulations (QSR’s) and ISO Standards. Write and/or execute Installation Qualifications (IQ), Operational Qualifications (OQ), Performance Qualifications (PQ), Validations, Design of Experiment (DOE), Process Failure Mode Effects Analysis (PFMEA), Process Master Validation Plans and Continuous Improvement studies/evaluations. Provide day to day technical floor support by investigation and resolution of issues that arise during the manufacturing process. etc. | 10/31/2020 |
| 9805 | Nova Biomedical Waltham, MA Reagent Test Assistant Unspecified Exp: 0-2 years |
The Reagent Test Assistant will perform testing of various calibrators, controls, and additional reagents required to support company produced and OEM analyzers, by means of verbal and/or written instruction under the supervision of the Group Leader/Supervisor. Train in the setting up, qualification, operation and troubleshooting of various analyzers and lab equipment. Record and report results as to whether the reagent/control has met specification to the Group Leader/Supervisor of Test lab. Train in performing titrations, pH measurements, flame photometry, microbial culture test and viscosity. Assist in cleaning of Test Lab to ensure work area is neat and safe. Read, write and able to follow instructions in English. etc. | 10/31/2020 |
| 9806 | Nova Biomedical Waltham, MA Formulation Operator - Second Shift HS diploma or equivalent Exp: 0-2 years |
The Formulation Operator will work on our Second Shift and perform batch processing of various calibrators, controls, and additional reagents required to support company produced and OEM analyzers. Essential Responsibilities: formulation of various solutions including staging of tanks, weighing and mixing of chemicals per assembly procedures (AP's) and final batch adjustment and transfer of solutions. Perform incoming inspection of raw chemicals upon receipt, maintenance of formulation equipment and cleaning as needed. Ability to accurately document and complete records of batch formulations. etc. | 10/31/2020 |
| 9807 | Nova Biomedical Waltham, MA Formulation Operator - First Shift HS diploma or equivalent Exp: 0-2 years |
The Formulation Operator will work on our First Shift and perform batch processing of various calibrators, controls, and additional reagents required to support company produced and OEM analyzers. Essential Responsibilities: formulation of various solutions including staging of tanks, weighing and mixing of chemicals per assembly procedures (AP's) and final batch adjustment and transfer of solutions. Perform incoming inspection of raw chemicals upon receipt, maintenance of formulation equipment and cleaning as needed. Ability to accurately document and complete records of batch formulations. etc. | 10/31/2020 |
| 9808 | Nova Biomedical Waltham, MA Reagent Packager I - First Shift HS diploma or equivalent Exp: 1+ year(s) |
The Packager, under general supervision, will follow established procedures in packaging reagent kits. This individual is responsible for working on an assembly line to assemble the various kits within the established quality and time standards. The individual will work with various packaging equipment such as: automated/manual tape machines, manual pallet trucks, conveyors, flow racks and other packaging devices. | 10/31/2020 |
| 9809 | Nova Biomedical Waltham, MA Replenishment Associate, Receiving HS diploma or equivalent Exp: 1+ year(s) |
The Receiving Replenishment Associate's is responsible for maintaining raw inventory within the raw material warehouse area. As part of the Receiving Team, the Replenishment Associate will be responsible for (1) the moving of raw material from the Receiving dock to the warehouse, (2) the consolidating of raw material in the warehouse, and (3) the picking and delivering of raw materials to the manufacturing floor. The Replenishment Associate will use documented procedures and good judgement to ensure inventory is stocked in an optimum manner, controlled, and ready for picking. Essential Responsibilities: Essential Responsibilities are to ensure the accurate movement (stocking, replenishing, consolidating, blocking, fulfilling) of materials and products within the Distribution Department and report any /all batch number or quantity discrepancies related to Distribution materials. etc. | 10/31/2020 |
| 9810 | Novo Nordisk Clayton, NC Manufacturing Process Technician I HS diploma/AS/AA Exp: 1+ year(s) |
Operate manufacturing equipment to achieve production goals. Accountabilities: Work in a safe and environmentally responsible manner. Setup, operate, monitor and control equipment, systems and processes. Execution of production schedule to achieve production goals. Maintaining aseptic areas and performing sanitizations environmental monitoring. Actively participate in and support event response. Reviewing and authoring Standard Operating Procedures (SOP’s) and other documents as required. Assist during equipment maintenance including restoration of lost function, predictive and preventative maintenance. etc. | 11/3/2020 |
| 9811 | Novo Nordisk West Lebanon, NH Quality Control Technician AS/AA Exp: 1 year |
Testing and laboratory operational support for Quality Control (QC) Good Manufacturing Practice (GMP) functions. Role focuses on support activities such as routine testing, sample and buffer preparation, laboratory inventory, waste management, material inspection, and general laboratory support. This position will be a Sunday - Thursday 8-5 p.m. schedule. Main Job Tasks: Sample receipt/login/inspection. Routine testing support as needed. Utility and cleaning sample testing via Total Organic Carbon (TOC) analyser. etc. | 11/3/2020 |
| 9812 | Novo Nordisk Clayton, NC Quality Control Technician I AS/AA Exp: 1+ year(s) |
Perform & review analysis of in-process, release & stability samples of Active Pharmaceutical Ingredient (API) and/or filled product in accordance with Current Good Manufacturing Practice (cGMP), site & corporate policies & procedures. Accountabilities: Accuracy & Scientific Soundness of Lab Data. Environmental Compliance. GMP Compliance of Laboratory. Maintain testing proficiency for methods. Timeliness of Lab Results & Investigations. Operational support of the QC Laboratory. etc. | 11/3/2020 |
| 9813 | Novo Nordisk Clayton, NC Filling Technician I - Day Shift HS diploma/AS/AA Exp: 1+ year(s) |
Filling of insulin and media preparations under aseptic conditions and operation of inspection equipment to achieve production goals. Accountabilities: Work in a safe and environmentally responsible manner. Operating, monitoring and controlling equipment, systems and processes associated with the Vial/Cartridge filling and inspection lines. Achieving production goals. Maintaining aseptic areas and performing sanitizations and environmental monitoring. Actively participate in and support event response. Reviewing and authoring Standard Operating Procedures (SOP’s) and other documents as required. etc. | 11/3/2020 |
| 9814 | Novo Nordisk West Lebanon, NH Manufacturing Technician Nights BS Exp: Not required for BS candidates |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to Current Good Manufacturing Practices (cGMPs), established manufacturing practices and procedures, and compliance with quality regulations and guidelines. Main Job Tasks: Product manufacturing and product manufacturing support activities. Completion of routine documentation associated with the manufacture of product. Support in-process activities and product development when instructed by supervisor. etc. | 11/3/2020 |
| 9815 | Novozymes Franklinton, NC Downstream Research Engineer, Global Optimization MS in chemical engineering Exp: Not necessary for MS candidates |
We’re seeking an energetic and self-directed person to join our Global Optimization Downstream team in the US. Your primary purpose is to have a focused effort on optimization of the downstream production processes to liberate capacity, reduce the variable cost, and improve product quality and robustness. You will contribute to Novozymes build-up in scientific and technical knowledge within downstream processing. In this role you’ll make an impact by: Testing improvement hypothesis at small scale and upscaling ones that prove successful. Leading projects to improve economies and capacities. Working together with Process Engineering and Operations to realize gains. etc. | 10/31/2020 |
| 9816 | NuVasive Memphis, TN Associate Material Handler - Distribution 1st Shift HS diploma or equivalent Exp: 1+ year(s) |
The Distribution Coordinator initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties. Compares nomenclature, stock numbers, and other listed information on packing slips to verify accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in process production reports, and status of material locations. etc. | 10/31/2020 |
| 9817 | NuVasive Memphis, TN Loaner Processing Technician - Surgical Device Sets HS diploma or equivalent Exp: <1 year |
Performs the physical or administrative tasks involved in the shipping, receiving, storing, distributing and order fulfillment of merchandise, products, materials, parts, supplies and equipment. Checks goods received and for distribution against purchase orders or invoices, maintains records of goods and rejects unsatisfactory items. Packages and prepares products and merchandise for final shipment and posts weights and shipping charges. Lifts heavy items and may operate a forklift. Prepares and maintains records of merchandise shipped. Reviews customer orders, examines, stocks and distributes merchandise, products and materials in inventory warehouses, distribution centers or manufacturing lines. Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties: Compares nomenclature, stock numbers, and other listed information on packing slips to verify accuracy of purchase orders and shipping orders. etc. | 10/31/2020 |
| 9818 | NuVasive Portland, OR Distributor, Sales Associate (Portland/Bend) BS/BA Exp: 1+ year(s) |
The Sales Associate is responsible for providing a wide variety of field sales support within an assigned geography while developing to become a sales specialist. Essential Responsibilities: Develop the required technical, clinical and sales competencies through the completion of the sales associate development program in order to qualify and meet the expectations of becoming a Sales Specialist within 18-24 months. Provide coordination and logistic support in properly ordering, transporting, setting up and reassembling surgical instrument sets inside sterile processing departments at hospitals and surgery centers. Act as a product support consultant to surgeons and operating room staff during surgical procedures in the safe and proper use of NuVasive® products and related surgical techniques. Support and contribute to the growth of revenues in assigned Sales Specialists territories through delegated business development activities with surgeons, hospitals and related staff. etc. | 10/31/2020 |
| 9819 | NuVasive Chicago, IL Sales Associate (Chicago, IL) BS/BA Exp: 1+ year(s) |
The Sales Associate is responsible for providing a wide variety of field sales support within an assigned geography while developing to become a sales specialist. Essential Responsibilities: Develop the required technical, clinical and sales competencies through the completion of the sales associate development program in order to qualify and meet the expectations of becoming a Sales Specialist within 18-24 months. Provide coordination and logistic support in properly ordering, transporting, setting up and reassembling surgical instrument sets inside sterile processing departments at hospitals and surgery centers. Act as a product support consultant to surgeons and operating room staff during surgical procedures in the safe and proper use of NuVasive® products and related surgical techniques. Support and contribute to the growth of revenues in assigned Sales Specialists territories through delegated business development activities with surgeons, hospitals and related staff. etc. | 10/31/2020 |
| 9820 | NuVasive Philadelphia, PA Sales Associate (Philadelphia, PA) BS/BA Exp: 1+ year(s) |
The Sales Associate is responsible for providing a wide variety of field sales support within an assigned geography while developing to become a sales specialist. Essential Responsibilities: Develop the required technical, clinical and sales competencies through the completion of the sales associate development program in order to qualify and meet the expectations of becoming a Sales Specialist within 18-24 months. Provide coordination and logistic support in properly ordering, transporting, setting up and reassembling surgical instrument sets inside sterile processing departments at hospitals and surgery centers. Act as a product support consultant to surgeons and operating room staff during surgical procedures in the safe and proper use of NuVasive® products and related surgical techniques. Support and contribute to the growth of revenues in assigned Sales Specialists territories through delegated business development activities with surgeons, hospitals and related staff. etc. | 10/31/2020 |
| 9821 | NuVasive Memphis, TN Assoc. Loaner Processing Technician HS diploma or equivalent Exp: 1+ year(s) |
Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties. Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in-process production reports, and status of material locations. Compiles information on receipt of disbursement of material, equipment, merchandise, or supplies, and computes inventory balance, price, and cost. etc. | 10/31/2020 |
| 9822 | NuVasive Memphis, TN Associate Assembler - 1st Shift HS diploma or equivalent Exp: 1+ year(s) |
The Associate Distribution Coordinator initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties: Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in-process production reports, and status of material locations. Compiles information on receipt of, disbursement of material, equipment, merchandise, or supplies, and computes inventory balance, price, and cost. etc. | 10/31/2020 |
| 9823 | Omeros Seattle, WA Research Associate I, Biochemistry BS Exp: 0-2 years |
As the Research Associate I, Biochemistry, your responsibilities include: Perform a variety of routine and non-routine research assignments as supervised by a PhD scientist. Conduct routine molecular biology bench work (e.g. recombinant DNA techniques, construct generation and testing). Perform routine eukaryotic cell culture (e.g. cell passaging, viability determination and transfection). Purify recombinant protein samples from cells, using standard lysis and chromatographic techniques and characterization (e.g. SDS-PAGE, Western blotting and thermal shift assays). Keep detailed records of samples, experimental results in lab notebook and digital systems. Analyze and summarize data, present at internal meetings, and communicate regularly with managers and coworkers on experiment progress. etc. | 10/31/2020 |
| 9824 | On Target Laboratories West Lafayette, IN Lab Animal Technician BS Exp: 1+ year(s) |
On Target Laboratories, Inc. discovers and develops targeted intra-operative imaging agents which illuminate malignant lesions and other diseased tissue. These imaging agents can be used by surgeons to help identify additional cancerous lesions and more precisely guide surgical oncologic procedures across a broad range of cancer types, thereby improving cancer surgery by helping to reduce the risk of recurrence and surgical complications for patients. Responsibilities: Accepts designated, business-focus projects to research, propose ideas and solutions, and present project during the weekly meetings. Conduct tumor implantations in mice. Image tumors with optical imaging agents using IVIS or Ami HT Image stations. Proficiently conduct ex vivo tissue biodistribution studies, PK studies, drug toxicity studies. etc. | 10/31/2020 |
| 9825 | Ora Andover, MA Regulatory Operations Specialist I BS/BA in the applied or life sciences or communications Exp: 1 year |
The Regulatory Operations Specialist is responsible for assisting the Regulatory team in QC, document management, and submissions. This is a team and individual contributor role, reporting to the Manager of Regulatory. This position will work collaboratively with regulatory team. This position requires a strong technical background, a high degree of enthusiasm, enjoyment of working in a fast-paced environment, being self-motivated, and being able to use critical reasoning to solve problems and make decisions. etc. | 11/3/2020 |
| 9826 | Ora Andover, MA Vivarium Technician BS in a life science or related Exp: 1 year |
Ora’s Vivarium Technician work in our pre-clinical in vivo labs and follow the standard operating procedures for animal care and husbandry in accordance to our IACUC protocols. The Vivarium Technician is responsible for providing enrichment, cleaning/washing housing, and feed study animals and assisting with ophthalmic animal research to support laboratory tasks for preclinical pharmacology studies, in collaboration with research associates. This work primarily includes but is not limited to animal dosing and assisting staff members with clinical observations, ophthalmic exams, ordering/receiving animal supplies, and preparing study binders. At Ora, the Vivarium Technician also supports dosing, animal handling, and data collection for study reports for the Veterinarian staff and research staff. etc. | 11/3/2020 |
| 9827 | OraSure Technologies Bethlehem, PA Scientist I BS in chemistry or biology Exp: Not necessary for BS candidates |
Individual has the responsibility to work in the laboratory to help carry out specific R&D projects. Individual will work with a Sr. Scientist or a Scientist II to carry out the required lab work, help prepare reports on results, maintain laboratory notebooks according to GLPs and help prepare necessary documents for product transfer to manufacturing. This is primarily a hands-on laboratory position. Some of the work will be somewhat repetitive. Responsibilities: Doing laboratory experiments, under the direction of a Scientist II or Sr. Scientist, to develop new and improved products. Occasionally help plan experiments. etc. | 11/3/2020 |
| 9828 | OraSure Technologies Bethlehem, PA Warehouse Associate I HS diploma or equivalent Exp: 1-2 year(s) |
Working under general supervision receives inbound freight and delivers materials and supplies to operating departments; prepares outbound shipments. Routinely performs additional tasks as may be required or assigned. Responsibilities: Pick, pack, and ship domestic and international orders according to quality and shipping procedures. Loads and unloads material from trucks or within a warehouse or storage facility. Receives freight and checks for damaged or defective goods. Delivers materials, supplies, and equipment to operating departments. Fill material requirements from manufacturing. etc. | 11/3/2020 |
| 9829 | OraSure Technologies Bethlehem, PA Quality Control Specialist I AS in chemistry, biology, medical technology, or related Exp: 1 year |
Quality Control Specialist I personnel perform procedures that include evaluation of raw materials, in-process components, finished products, stability testing, equipment quality control, and equipment maintenance in compliance with guidelines established by Orasure Technologies and regulatory agencies. This position is on a 2nd shift M-F 2:30-11pm with training on 1st shift M-F 6:30am-3pm. Responsibilities: Perform all procedures accurately and according to written Work Instructions and SOPS as indicated in the Quality Control procedures and other applicable facility procedures. Perform testing at all levels of production including raw materials, in-process components, finished products and stability testing. Perform visual finished product inspections. etc. | 11/3/2020 |
| 9830 | Pacira BioSciences San Diego, CA Microbiologist 1 BS in microbiology or other life science Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products. Responsibilities: Conduct routine environmental and systems monitoring of manufacturing and laboratory areas. Conduct general laboratory experimentation in compliance with the instructions provided in approved SOP’s to determine appropriate action. Follow policies and assists in the development of new procedures and/or documents. Maintain records of experiments performed and results obtained including appropriate calculations. Assist in the interpretation of data as require and conduct accurate and precise experimentation and complete. etc. | 11/3/2020 |
| 9831 | Pall Pensacola, FL Operator II HS diploma or equivalent Exp: 1-2 year(s) |
A Production Operator II is proficient in the independent set-up, start-up, continuous operation and shutdown of your assigned area process or processes as detailed by your Value Stream (VS). Essential Job Duties: Set-up, start-up, continuous operation and shutdown of manufacturing equipment and processes, using adherence to Standard Work Instructions (SWIs), Good Manufacturing Practices (GMP) and current Good Documentation Practices (cGDP). Monitor Critical-to-Quality (CTQs) media metrics, e.g. Delta-P, KL, Thickness, Basis Weight, etc. through Statistical Process Control (SPC) – where applicable – to ensure the highest quality media possible. When appropriate, perform adjustments to the process using formally detailed and approved Corrective Methods (CMs). Advance any manufacturing process issues in a timely manner to minimize scrap and downtime. etc. | 11/3/2020 |
| 9832 | Pall Putnam, CT Night Shift Production Operator II HS diploma or equivalent Exp: 1-2 year(s) |
An Operator II supporting our Night Shift is proficient in the set-up, start-up, continuous operation and shutdown of the assigned Value Stream manufacturing equipment and processes using adherence to Standard Work Instructions, Good Manufacturing Practices and current Good Documentation Practices. Essential Job Duties: Work overnight shift 4 days/week (includes a shift differential). Follow all practices and procedures regarding safety and quality compliance including OSHA, cGMP, ISO 9001 & ISO 14000 requirements. Find and suggest opportunities to improve when possible. Follow a weekly schedule and showcase strong attendance reliability. Read, Follow and support the training of other associates on Standard Operating Procedures. Develop proficiency of requisite manufacturing processes and most equipment through on-the-job training and be able to assist in training other associates in Value Stream. etc. | 11/3/2020 |
| 9833 | Pall Pensacola, FL Production Operator II HS diploma or equivalent Exp: 1-2 year(s) |
A Production Operator II is proficient in the independent set-up, start-up, continuous operation and shutdown of your assigned area process or processes as detailed by your Value Stream (VS). Essential Job Duties: Set-up, start-up, continuous operation and shutdown of manufacturing equipment and processes, using adherence to Standard Work Instructions (SWIs), Good Manufacturing Practices (GMP) and current Good Documentation Practices (cGDP). Monitor Critical-to-Quality (CTQs) media metrics, e.g. Delta-P, KL, Thickness, Basis Weight, etc. through Statistical Process Control (SPC) – where applicable – to ensure the highest quality media possible. When appropriate, perform adjustments to the process using formally detailed and approved Corrective Methods (CMs). Advance any manufacturing process issues in a timely manner to minimize scrap and downtime. etc. | 11/3/2020 |
| 9834 | Par Pharmaceutical Rochester, MI Process Engineer I MS in chemical or other engineering Exp: 1+ year(s) |
The Process Engineer I, with guidance, performs various duties related to optimization and analysis of production processes, new products, processes and technology transfers. Prepare and execute engineering study protocols, manufacturing and packaging experimental / feasibility study / validation batch records and protocols and complete interim and / or final summary reports for marketed and new products. Perform or assist on-site and site-change technical transfer, scale-up or scale-down factor evaluation, manufacturing / packaging process and equipment troubleshooting, and SOP preparation and review. Process Engineering duties within a single location. Make decisions within guidelines and policies. Follow established procedures to perform assignments, with general instructions on the process and desired outcome. Work is reviewed for soundness of technical judgment and accuracy. etc. | 11/3/2020 |
| 9835 | Myriad Austin, TX Research Associate I BS Exp: 0-5 years |
Plan, perform, evaluate the process of manufacturing reagents. Principal Responsibilities: Manufacture reagents required for the testing of samples, including but not limited to coupling of antibody to beads, biotinylation of antibody for detection, testing of minipool and simplex reagents, batching and qualification of new lots of batched reagents, and troubleshooting problematic reagents. Conduct assigned experiments and assists in their designs. Follow directions and laboratory procedures as assigned by supervisor. Analyze, interpret, and report results. Help to complete projects on time and within budget. Support transition of methods and reagents to customers. Serve as expert in area of specialization in relations with other scientific personnel. etc. | 10/25/2020 |
| 9836 | Myriad Salt Lake City, UT Intake Associate (Remote) HS diploma or equivalent Exp: 6-12 months |
Responsibilities: Translate critical healthcare information and test orders from test request forms into database accurately and timely. Review received orders for required elements and effectively communicate missing elements. Ensure a high level of quality throughput. Complies with applicable CLIA and HIPAA regulations. etc. | 10/25/2020 |
| 9837 | NAMSA Northwood, OH Animal Care Technician HS diploma or equivalent Exp: 0-2 years |
Principal Duties and Responsibilities: Primarily involved in the welfare and husbandry activities of animals, including sanitation of equipment and the vivarium. Receives, identifies, and acclimates laboratory animals. May euthanize animals. May administer medications under the direction of a Veterinarian. Follows the Quality Manual, all NAMSA SOPs, and Process documents. Documents all required tasks. May administer treatments as directed by staff veterinarian. May conduct training on husbandry tasks for other Associates and update training records. etc. | 10/25/2020 |
| 9838 | NAMSA Irvine, CA Microbiology Technologist BS/BA Exp: No experience required |
Principal Duties and Responsibilities: May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. May be required to operate autoclave, depyrogenation oven or other specified laboratory equipment. etc. | 10/25/2020 |
| 9839 | NAMSA Northwood, OH Lab Technologist - In Vivo BS/BA Exp: Not necesary for BS/BA candidates |
Principal Duties and Responsibilities: May prepare all testing/test article and animals according to written instructions and protocols. May execute routine testing per NAMSA SOPs, with appropriate data analysis. May communicate test schedule updates to NAMSA management as needed. May prepare and maintain reagents and/or test articles as required for testing. Maintain ancillary records (log books, worksheets). Maintain relevant supplies and equipment used in routine testing. Routes all positive results or unusual testing occurrences to management. May be required to conduct daily health observations. May be required to administer the test article or extract according to written instructions. etc. | 10/25/2020 |
| 9840 | NAMSA Northwood, OH Chemist MS/MA Exp: Not necesary for MS/MA candidates |
Principal Duties and Responsibilities: Independently conduct testing according to written instructions. May be requested to conduct more involved studies. May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. May conduct routine testing per NAMSA SOPs as well feasibility, protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP, etc. Works with management to ensure large studies are completed on or before the due date. Prepare and maintain the reagents required for testing. May mentors and train staff in general laboratory testing as well as offering more complex instrumentation training. etc. | 10/25/2020 |
| 9841 | NAMSA Irvine, CA Microbiology Technologist - Sterility Assurance BS/BA Exp: Not necesary for BS/BA candidates |
Principal Duties and Responsibilities: May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. etc. | 10/25/2020 |
| 9842 | Nanomix Emeryville, CA Research Associate BS in chemistry, chemical engineering, biology, bioengineering, or related Exp: 3 months |
Design and develop new cartridge prototypes, working with biosensors, filters, conjugate pads, microfluidics, device programming, etc. to enable specific biological assays on the eLab platform. Design processes required to manufacture product components by developing fixtures (CAD, Laser Printer, 3D Printer, Solidworks etc.), installing necessary components on machinery (Vacuum, Pressure Gauge, Pressure Regulator etc.), scripting robotic liquid handlers, drafting qualification requirements, and writing quality documentations. Design and execute biological wet lab experiments using ELISA, enzymatic assays, chromogenic assays, fluorescence/chemiluminescence. Work with electrochemical (CV, chronocoulommetry) and analytical (FTIR, Raman) tools to characterize biosensors and their performance. Develop quality control methods and implement them in the quality system. etc. | 10/25/2020 |
| 9843 | Nanostring Bothell, WA Kitting Associate I Unspecified Exp: 0-2 years |
The Kitting Associate I is responsible for kitting customer orders. Essential Duties: Accept receipt of products and ensure that materials are in good condition. Unpack and check goods received against purchase orders or invoices. Operate effectively in our ERP system for goods receipts and to create and process production orders and shipments. Maintain all records related to incoming goods. Reject unsatisfactory items as required, and assess the need to file claims with carrier. Participate in weekly cycle counts, and assist with reconciliation of item variance. Kitting raw materials into finished goods using Standard Operating Procedures. Process customer orders through the NAV ERP system. Verify inventory locations and availability for shipment against requirements specified in purchase orders. etc. | 10/25/2020 |
| 9844 | Nanostring Seattle, WA Process Engineer II MS Exp: Not necessary for MS candidates |
Summary: The Process Engineer II is responsible for developing, implementing, and troubleshooting new methods used in manufacturing in support of the release of new products. This individual will assist in design, development, and scale-up of processes, instruments, and equipment from the laboratory through the pilot plant and manufacturing process. This individual may establish operating equipment specifications and improve manufacturing techniques. In addition, this individual is involved in new product development, process improvement, and design transfer activities, and may serve as a Process Development lead on project teams. Essential Responsibilities: Develop methods for the manufacturing and use of NanoString products. Develop and draft SOPs, Batch Records, Specifications, and other documentation associated with process transfer to a Manufacturing environment. Assist with performing and documenting Risk Assessments. Assist with design, document and summarize Verification and Validation studies. Draft protocols, experimental summary reports, quality documents and other scientific literature associated with projects. etc. | 10/25/2020 |
| 9845 | Nanostring Bothell, WA Instrumentation/Calibration Tech I BS Exp: 1+ year(s) |
Summary: The Instrumentation/Calibration Tech I is responsible for the maintenance, testing, troubleshooting, calibration, and repair of a variety of circuits, components, analytical equipment, and instrumentation for laboratory and manufacturing equipment Requirements: Minimum 1 year of experience in the biotech or life sciences field Bachelor of Science degree in a relevant science or engineering related field or commensurate experience Basic computer skills (Excel, Word) and good communication skills Ability to work both as part of a team and independently Ability to lift a minimum of 50 lbs Valid Washington driver’s license. etc. | 10/25/2020 |
| 9846 | Natera San Carlos, CA QC Reagent Associate I BS in biology, chemisry, or related Exp: 0-1 year(s) |
Executes the preparation and qualification of molecular diagnostic reagents. Performs Quality Control tests on new incoming shipments of raw materials and small scale manufacturing procedures (formulations and dispensing) reagent. Reviews data obtained for compliance to specifications and reports abnormalities. Maintains and improves QC documentation pertaining to raw material specification, reagent qualification, and QC testing. etc. | 10/25/2020 |
| 9847 | Natera Austin , TX IQC-Reagents Associate 1 HS diploma or equivalent Exp: 1+ year(s) |
Support the activities for reagents used in the Operations Department’s Clinical Laboratories, which includes but is not limited to incoming material inspections to assure product safety and compliance to specifications, GMP’s, and ISO requirements. PRIMARY RESPONSIBILITIES: Coordinate labeling and prep for reagents following standard operating procedures with little to no errors. Receive, verify, label, store reagents according to department procedures. Responsible for ensuring reagents are stored in appropriate conditions. Ensures all dispenses are qualified and accounted for. Verify that data is properly entered into laboratory inventory system. etc. | 10/25/2020 |
| 9848 | Natera San Carlos, CA Equipment Lab Technician BS/BA Exp: 0 years |
The Equipment Laboratory Technician will join the QC Equipment team in the Operations department to support the equipment used in the clinical laboratories. Responsibilities will include activities related to the maintenance of accessory equipment used in the Operations lab. PRIMARY RESPONSIBILITIES: Receive and label new equipment according to department procedures. Update and upkeep equipment inventory. Coordinate calibration schedule for all accessory equipment with appropriate in-house personnel or outside vendors. Execute and document maintenance performed on accessory equipment based on recommended intervals. Maintain calibration and maintenance records. etc. | 10/25/2020 |
| 9849 | Natera Austin , TX QC Equipment Specialist I BS/BA Exp: 0-2 years |
Supports equipment and instrumentation utilized in the Operations laboratory. The QC Equipment Specialist is the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. PRIMARY RESPONSIBILITIES: Provide support for general lab equipment failures in the clinical lab to minimize downtime. Assist with diagnosis, service, and preventative maintenance on instrumentation. Coordinate scheduled and unscheduled maintenance activities, including calibration/preventive maintenance, with approved service provider. Act as point of contact and responsible party for scheduled and unscheduled equipment maintenance. Perform calibration checks on general laboratory equipment based on recommended intervals. Develop and execute procedures for the cleaning and maintenance of laboratory equipment. Execute qualification for new and/or returning laboratory equipment. etc. | 10/25/2020 |
| 9850 | Natera San Carlos, CA Clinical Sample Associate I BS/BA Exp: 1 year |
At Natera we are pushing the limits creating exciting products and changing lives. We are seeking a highly motivated and team oriented individual to join the Scientific Operations team as a Clinical Sample Associate 1 to be a part of this exciting team! The ideal candidate must be detail-oriented and have an outstanding ability to perform routine laboratory research and development services. The Clinical Sample Associate 1 will work with a multidisciplinary team in a high-performance environment. PRIMARY RESPONSIBILITIES: You will work primarily with the R&D Scientific Operations team maintaining commercial sample operations for research use. Manage commercial samples transfer into R&D biobank. Verify eligibility for research use based on retention policies, patient opt-outs, and legal requirements. etc. | 10/25/2020 |
| 9851 | Natera Austin, TX Clinical Laboratory Operator I BS/BA Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: Assist in testing of patient samples according to standard operating procedure. Meet expected performance metrics within role as applicable. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Provide guidance for new team members. Follows GLP (good laboratory practice): maintain clean and organized workspace. Completes training and other deadlines on time. Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory’s standard operating procedures. Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor. Communicates with team and other departments on various platforms (including via e-mail). etc. | 10/25/2020 |
| 9852 | Natera San Carlos, CA Clinical Laboratory Associate I (Temporary) BS/BA Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate I (Temporary) to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. PRIMARY RESPONSIBILITIES: Assists in testing of patient samples according to standard operating procedure in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Follows GLP (good laboratory practice): maintain cleans and organized work space. Completes training and other deadlines on time. Recognizes and escalates equipment malfunctions; troubleshoots common errors on the lab floor. Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor. Communicates with team and other departments (including via e-mail). Provides feedback on day-to-day schedule and tasks to lead/supervisor. etc. | 10/25/2020 |
| 9853 | Natus Medical Middleton, WI Product Technician II AS/AA Exp: 1-2+ year(s) |
Primary Responsibilities for Production Technician II: Perform repetitive production work including configuring computers and hardware systems, loading, configuring and licensing of software. Perform standard production test routines using computerized and functional test equipment. Perform troubleshooting to identify the source of failures and resolve problems. Capture data, verify conformance to specifications and document results. Assist with other production assembly and stockroom work as required. Assist with engineering lab projects from time-to-time. Stay up-to-date and follow all Quality System procedures related to this job, which can affect the quality of products or services provided to our customers. etc. | 10/27/2020 |
| 9854 | Natus Medical Middleton, WI Assembly Associate II HS diploma or equivalent Exp: 3-6 months |
Primary Responsibilities: Perform a variety of tasks including repetitive and non-repetitive production which may include assembly of components, kitting of parts and configuring assemblies. Conduct quality inspections on in-process materials. Complete documentation and other paperwork as part of the production process. Assist with stockroom and shipping work as required. Stay up to date and follow all Quality System procedures related to this job, which can affect the quality of products or services provided to our customers. etc. | 10/27/2020 |
| 9855 | Nemera Buffalo Grove, IL Operator Technician HS diploma or equivalent Exp: 6+ months |
As a result of large organizational growth as well as the recent COVID-19 pandemic, Nemera is committed to helping our patients during this time of need. Be a part of the solution from the beginning and join our team as a Machine Operator in Buffalo Grove, IL! Open 24 hours and running on two-12 hour shifts from either 6pm-6am OR 6am-6pm on a 2-2-3 rotating schedule, both shifts are currently available. As a Machine Operator with Nemera, you'll operate assembly or injection molding equipment, solve equipment issues, and package the molded components or assembled products based on company and customer specifications. etc. | 10/27/2020 |
| 9856 | NeoGenomics Ft. Myers, FL Clinical Laboratory Technologist - Flow Cytometry BS in medical technology or other chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist - Flow Cytometry you will work under general supervision. You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 9857 | NeoGenomics Carlsbad, CA Clinical Laboratory Technologist - Temporary, Covid Department BS in medical technology or other chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist you will work under general supervision. You will be responsible for performing highly complex laboratory testing procedures involving Covid-19 patient samples. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 9858 | NeoGenomics Ft. Myers, FL Clinical Laboratory Technologist, FISH - Friday - Monday, 10hr Shifts BS in cytogenetics or other chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist – FISH you will work under general supervision. You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. The shift for this position will be Friday - Monday days, days, 10hr Shifts. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 9859 | NeoGenomics Ft. Myers, FL Clinical Laboratory Technologist, FISH, Sun-Thur 8:00 am - 4:30 pm BS in cytogenetics or other chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist – FISH you will work under general supervision. You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. The shift for this position will be Sunday-Thursday 8:00 am - 4:30 pm: Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 9860 | NeoGenomics Ft. Myers, FL Clinical Laboratory Technologist, Flow Cytometry, Mon - Fri 11:00pm - 7:30am BS in a chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist Flow Cytometry you will work under general supervision. You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. The shift for this position will be Monday - Friday 11:00pm - 7:30am. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 9861 | NeoGenomics Aliso Viejo, CA Histotechnologist I, Tues-Sat 9am-5:30pm AS/BS in histopathology Exp: Not necessary for AS/BS candidates |
As a Histotechnologist you will work under general direction to precisely and accurately conduct a variety of routine and specialized histology procedures. You will research, troubleshoot, and resolve histology related inquiries and problems within the laboratory. This position requires you to produce the highest quality of embedding, microtomy, tissue grossing, tissue processing, and H&E staining, special staining and equipment maintenance. etc. | 10/27/2020 |
| 9862 | NeoGenomics Aliso Viejo, CA Histotechnologist, Tues-Sat 9pm-5:30am AS/BS in histopathology Exp: 1+ year(s) |
As a Histotechnologist you will work under general direction to precisely and accurately performing a variety of routine and specialized histology techniques and procedures. In this role, you will receive specimens, prepare them for testing and analysis, and perform filing to finish the case. You will research, troubleshoot, and resolve histology related inquiries and problems within the laboratory. This position requires you to produce the highest quality of embedding, microtomy, tissue grossing, tissue processing, and H&E staining, special staining and equipment maintenance. Receive specimens of tissue and ensure proper accessioning and labeling of all tissue samples. Process paperwork associated with accessioning and reporting. Prepare tissue specimens with chemicals, slicing, and mounting on glass slides for microscopic examination and analysis. etc. | 10/27/2020 |
| 9863 | Nephron Pharmaceuticals West Columbia, SC Instrument Specialist/Chemistry Lab BS/BA Exp: Not necessary for BS/BA candidates |
Oversees all aspects of the laboratory instrumentation in the chemistry laboratory. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. Relies on experience and judgment to plan and accomplish goals. Performs a variety of complicated tasks under general supervision for which creativity is expected and latitude is given. Primary Accountabilities: NOTE: The Primary Accountabilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager. Plans, organizes, and manages preventative maintenance of laboratory equipment. Creates or modifies SOPТs, forms, logbooks, etc. as necessary to facilitate the instrumentation program. Ensures that supplies are on hand to perform routine instrument maintenance and that supplies for non-routine maintenance or troubleshooting are ordered promptly as needed. etc. | 10/27/2020 |
| 9864 | Nexcelom Bioscience Lawrence, MA Sales Development Representative BS/BA in the life sciences, business, or related Exp: 1+ year(s) |
Nexcelom has an immediate opening for a Sales Development Representative [SDR] in our Lawrence, Massachusetts Headquarters. The SDR will partner with marketing and sales to grow revenue and drive in-house lead generation, appointment setting, lead qualification, remote demos and sales support to the Field Sales team. This position requires heavy outbound phone calling, qualification, consultative selling skills and tight collaboration with the Field Sales team to generate new clients and maintain the existing customer base. The SDR will be expected to manage a pipeline and report on qualification and call activity. etc. | 10/27/2020 |
| 9865 | NexImmune Gaithersburg, MD Research Associate/ Senior Research Associate in Cell Biology/Immunotherapy BS/MS in immunology, biology, biochemistry, or other life science Exp: 1-3 year(s) |
The Research Associate/ Senior Research Associate in Cell Biology/Immunotherapy will act as a scientific contributor for the Preclinical Immunotherapy Department developing and optimizing a new clinical approach to adoptive T cell therapy, based upon NexImmune’s proprietary artificial Antigen Presenting Cell (aAPC) technologies. The candidate will assist in the generation and phenotypical and functional characterization of antigen-specific T cells. Laboratory skills, notebook recording/maintenance, and writing of reports in acceptable scientific format(s) are important. etc. | 10/27/2020 |
| 9866 | Nitto Milford, MA Quality Control Environmental Analyst I BS in chemistry, biology, or related Exp: 0-2 years |
The QC Environmental Analyst I supports manufacturing operations by performing environmental monitoring of the cleanrooms, and sampling and testing of the water system, as well as perform additional microbial sampling and testing as required. The position works within the QC lab on assigned tasks following written procedures and protocols. The position also assists in the maintenance of overall laboratory systems. Key Job Responsibilities: Perform water sampling as required per current procedures. Perform Environmental Monitoring as required per current procedures. Initiate Alert and Action documents as required. Coordinate with contract labs as appropriate for sample pickup and material drop off. Data reporting, and maintaining water trending and environmental monitoring data charts and tables. etc. | 10/27/2020 |
| 9867 | Nitto Milford, MA Quality Control Analyst I/II/III BS/MS in chemistry, biology, or related Exp: 0-7 years |
The position involves the performing of routine and non-routine analyses of raw materials, in-process materials and finished products in accordance with cGMP guidelines. The appropriately trained individual may provide training and guidance to other QC Analysts. The individual troubleshoots problems associated with methods and instruments resolving them where possible or seeking guidance/authorization where required. Key Responsibilities: Test and analyze samples in a timely manner in support of project plans in accordance to cGMP guidelines. Review analytical data for compliance with specifications and cGMP guidelines. Assist in development of experimental procedures and protocols. Develop/revise documentation such as SOP, testing procedures and material specifications. etc. | 10/27/2020 |
| 9868 | Nitto Milford, MA 1st shift-Temp to Hire Manufacturing Chemist I/II HS diploma or equivalent Exp: Entry level |
Purpose of Position: Responsible for the implementation of assigned production procedures working within defined production schedules. Responsible for performing all work within company and cGMP regulatory compliance. Maintaining a safe work environment and following all site safety procedure. Participation as a member of a safety team. Performs routine, generally highly structure work. Responsible for staying current with the prescribed training curriculum specified for the job title. etc. | 10/27/2020 |
| 9869 | Nkarta South San Francisco, CA Cell Therapy Associate AS/BS in a relevant science or engineering Exp: 1-3 year(s) |
Working with other members of the manufacturing team, this role supports the successful tech transfer and operational readiness processes including the GMP manufacture and release of cell therapy products. Key Responsibilities: Supports the successful tech transfer and operational readiness processes using knowledge of cGMP regulations to ensure manufacturing readiness. Supports the GMP manufacture and release of cell therapy products; follows all processes and procedures related to operations in full compliance with cGMP, CFRs, site quality systems and company policies; and promotes a culture of quality and compliance. Performs process unit and support operations described in standard operating procedures (SOPs) and batch records including: media and solution preparation, cell drug substance preparation; and drug product fill operations. Performs all tasks associated with the manufacture of commercial product following batch records and SOPs. Works as part of a small team to execute GMP runs in close collaboration with process development and quality. etc. | 10/27/2020 |
| 9870 | Nordson East Providence, RI Machine Technician - 2nd shift HS diploma or equivalent Exp: 1-3 year(s) |
Machine Technician I is responsible for setting up and operating specialized automated production assembly equipment as well as setting up manual jigs and fixtures for secondary operations. Additionally, responsible for detailed record keeping for equipment and production related activities. Essential Job Duties and Responsibilities: Setup and operate automated production equipment. Setup manual jigs and fixtures for production operators. Provide training and instruction to operators on proper equipment operation. Prepare all materials in advance of setup. etc. | 10/27/2020 |
| 9871 | Nordson Brooklyn Park, MN Product Development Technician Supervisor - Nordson MEDICAL AS/AA Exp: 1-3 year(s) |
The Product Development Technician Supervisor is responsible for planning and directing daily activities, in coordination with the Development team, of personnel focused on Development assembly. The supervisor supports goals and objectives according to GMP’s, SOP’s and established policies, practices, procedures, quality, and cost standards. The role focuses on continuously improving efficiencies and working cross functionally to achieve overall company objectives. Essential Job Duties and Responsibilities: Participate in Development project planning to understand upcoming Development needs, changes in schedules, current challenges, and space/equipment allocation to help establish strategies to meet team goals. etc. | 10/27/2020 |
| 9872 | Nordson Brooklyn Park, MN Production Operator I HS diploma or equivalent Exp: No experience required |
Position consists of assembling and inspecting medical devices in a clean room environment while under general supervision in accordance with specific work instructions and SOPs. Assembly and inspection sometimes done under a microscope. This position requires the ability to work with small tools and assemble small components using a high degree of dexterity and accuracy. This position requires direct contact with an implantable medical device. Essential Job Duties and Responsibilities: Must be able to work under direct supervision and take work instruction from Supervisor and Leads, work cooperatively and productively within a team environment. etc. | 10/27/2020 |
| 9873 | Nordson Austintown, OH Material Handler HS diploma or equivalent Exp: 1-3 month(s) |
A material handler is responsible for sequencing all WIP, driven by dispatch scheduling, at each relevant machining center to enable work center efficiency and elevate execution of OTD to 90% or greater. Essential Job Duties and Responsibilities: Offloads incoming bar stock. Moves bar stock from storage area into the manufacturing process as required. Reviews machining center daily dispatch reports for machining centers and sequences bar stock in order at the relevant machining center. Transfers bar stock from machining center to machining center to assist operator efficiency. Removes clutter from the process line areas. Removes and disposes of dunnage properly. Empties machining chip hoppers as necessary. etc. | 10/27/2020 |
| 9874 | Meridian Bioscience Cincinnati, OH Senior Research Associate MS Exp: 1 year |
The immunoassay function within R&D is responsible for developing the next generation diagnostic kits for Meridian. The Senior Research Associate will support the development of a new diagnostic device as part of an assay team. Responsible for designing and executing experiments, acquiring data, drawing conclusions for discussion and recommendations. Key Duties: Supports the technical work of a project – execute experiments. Participates in brainstorming discussions and sharing ideas with the team. Presentations – present data during team meetings. Data analysis – review the data generated by a given study and draw conclusions. Documentation ownership – write protocols, reports and any other documentation needed for the support of the project. etc. | 10/20/2020 |
| 9875 | Merieux NutriSciences Allentown, PA Microbiology Technician AS/AA/BS/BA Exp: 1+ year(s) (AS/AA); 0 years (BS/BA) |
Your mission will be to: Job Duties: Read plates and tubes, as required, to determine the number of organisms in the sample. Record findings on worksheet for verification. Write identification onto plates so that client and sample number can be tracked. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Prepare sample for analysis by recording, weighing, and blending. Collect plates and place them in the incubator for the specified amount of time and temperature. Prepare media and broth for use in pathogen testing as required. etc. | 10/20/2020 |
| 9876 | Merieux NutriSciences Salida, CA Chem Tech AS/AA/BS/BA Exp: 1+ year(s) (AS/AA); 0 years (BS/BA) |
Your mission will be to: Job Duties: Composting and grinding of samples for analysis as required. Perform chemical analyses such as protein, moisture, fat, ash, and other components. Prepare sample for analysis according to procedure. Retrieve samples from designated areas (e.g. log-in, sample storage). Perform chemical analyses of macronutrients, micronutrients or other parameters as designated. Extract desired component from sample with appropriate processes so that concentration can be determined. Prepare standards and reagents that are needed for the analysis procedure. Write/label all samples throughout the process so that Client and sample numbers can be tracked. Perform calculations, checking and interpretation of results where applicable. etc. | 10/20/2020 |
| 9877 | Merieux NutriSciences Crete, IL Chemist I Unspecified Exp: 1-2 year(s) |
The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. This position reports to the Supervisor of Chemistry. Job Responsibilities: Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. Wash glassware as needed and prepare samples as needed. etc. | 10/20/2020 |
| 9878 | Merieux NutriSciences Crete, IL Chemist III MS Exp: 1-2 year(s) |
The incumbent is responsible for performing chemical analysis on food, pharmaceutical, and other sample. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the sample to obtain the required results. The incumbent observes daily activities of departmental personnel ranging from receiving to reporting of results and ensures that analysis is performed correctly. Performs high end analyses with instrumentation (GCMS, LCMS, HS-LCMS, etc.) autonomously. Utilize various instruments such as LCMS, GCMS, HPLC, ICP, ICPMS, and GC to determine concentration of desired balances in the food sample. This position has the responsibilities and authority to identify departures from the quality system or test procedures and document such observation accordance with the prescribed complaint system. etc. | 10/20/2020 |
| 9879 | Merieux NutriSciences Stone Mountain, GA Microbiology Technician AS/AA/BS/BA Exp: 1+ year(s) (AS/AA); 0 years (BS/BA) |
Your mission will be to: Job Duties: Read plates and tubes, as required, to determine the number of organisms in the sample. Record findings on worksheet for verification. Write identification onto plates so that client and sample number can be tracked. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Prepare sample for analysis by recording, weighing, and blending. Collect plates and place them in the incubator for the specified amount of time and temperature. etc. | 10/20/2020 |
| 9880 | Merieux NutriSciences Cypress, CA Microbiology Technician AS/AA/BS/BA Exp: 1+ year(s) (AS/AA); 0 years (BS/BA) |
Your mission will be to: Job Duties: Read plates and tubes, as required, to determine the number of organisms in the sample. Record findings on worksheet for verification. Write identification onto plates so that client and sample number can be tracked. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Prepare sample for analysis by recording, weighing, and blending. Collect plates and place them in the incubator for the specified amount of time and temperature. Prepare media and broth for use in pathogen testing as required. etc. | 10/20/2020 |
| 9881 | Merieux NutriSciences Gainesville, FL Chemist AS/AA/BS/BA Exp: 1-2 year(s) |
The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. Job Duties: Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. etc. | 10/20/2020 |
| 9882 | Merit Medical South Jordan, UT Technician III BS/BA Exp: 1 year |
Performs non-routine technical assignments of substantial variety and complexity. ESSENTIAL FUNCTIONS PERFORMED: Performs assignments and may assist in planning assignments of a non-routine nature for which operational precedents are not fully applicable. Prepares test specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Extracts engineering or other data from various reports, processes the data, and presents the data. Receives technical advice from engineers or supervisor for complex problems. Working overtime may be required for this position. etc. | 10/20/2020 |
| 9883 | Merit Medical South Jordan, UT Molding Operator II HS diploma or equivalent Exp: 1+ year(s) |
This position is responsible for cosmetic part quality, dimensional charting, paperwork completion, and submission of molded component lots to Quality Assurance for final audit approval. ESSENTIAL FUNCTIONS PERFORMED: Performs start-up dimensions, as required. Packages and weighs the product and makes labels. Inspects parts visually and uses measuring tools; documents results and ensures compliance to drawings and specifications; performs testing of products, as required. etc. | 10/20/2020 |
| 9884 | Merit Medical South Jordan, UT Production Operator IV HS diploma or equivalent Exp: 6 months |
Performs a variety of complex medical assembly and processing tasks as a production team member, including performing various technical assembly tasks. ESSENTIAL FUNCTIONS PERFORMED: Perform all processes within quality specifications while visually monitoring the machines/equipment used to ensure proper function. Ability to rotate through the assembly line, performing all production assembly operations. Performs on-line and in-process visual inspection of products to ensure it meets specifications per work order and procedure instructions. etc. | 10/20/2020 |
| 9885 | Merit Medical Pearland, TX Production Operator II-Carton Assembly 2nd Shift HS diploma or equivalent Exp: 3-6 months |
Performs any of a variety of medical assembly and processing tasks as a production team member. ESSENTIAL FUNCTIONS PERFORMED: Assembles medical products on an assembly operation, performing a variety of tasks on a rotating basis. Ability to rotate through the assembly line. Performs on-line and in-process visual inspection of products to ensure specifications per work order and procedure are followed. Assists Team Leader and Technicians with product and/or machine change-overs. Ensures product assembled meets quality standards. etc. | 10/20/2020 |
| 9886 | Merit Medical South Jordan, UT Production Operator III HS diploma or equivalent Exp: 3 months |
Performs a variety of medical assembly and processing tasks as a production team member, including performing various technical assembly tasks. ESSENTIAL FUNCTIONS PERFORMED: May include but not limited to performing one or more processes within quality specifications while visually monitoring the machines/equipment used to ensure proper function. Ability to rotate through the assembly line, performing all production assembly operations. Performs on-line and in-process visual inspection of products to ensure it meets specifications per work order and procedure instructions. etc. | 10/20/2020 |
| 9887 | Merit Medical South Jordan, UT Production Operator III (Catheter Line) HS diploma or equivalent Exp: 3 months |
Performs a variety of medical assembly and processing tasks as a production team member, including performing various technical assembly tasks. ESSENTIAL FUNCTIONS PERFORMED: May include but not limited to performing one or more processes within quality specifications while visually monitoring the machines/equipment used to ensure proper function. Ability to rotate through the assembly line, performing all production assembly operations. Performs on-line and in-process visual inspection of products to ensure it meets specifications per work order and procedure instructions. etc. | 10/20/2020 |
| 9888 | Merit Medical South Jordan, UT Production Operator IV HS diploma or equivalent Exp: 6 months |
Performs a variety of complex medical assembly and processing tasks as a production team member, including performing various technical assembly tasks. ESSENTIAL FUNCTIONS PERFORMED: Perform all processes within quality specifications while visually monitoring the machines/equipment used to ensure proper function. Ability to rotate through the assembly line, performing all production assembly operations. Performs on-line and in-process visual inspection of products to ensure it meets specifications per work order and procedure instructions. etc. | 10/20/2020 |
| 9889 | MSD Rockville, MD Engineer I, Process BS in chemical or biochemical engineering Exp: 1+ year(s) |
Responsible for developing, characterizing and validating manufacturing processes to produce biochemical assay plates and related consumables. DUTIES AND RESPONSIBILITIES: Review existing manufacturing processes to determine if changes are needed to improve quality and quantity of products, reduce any variations between lots produced and expand product portfolio. Make recommendations to manager to improve/enhance processes as needed. Design and conduct process experiments on manufacturing and pilot scale equipment to determine if/how changes affect product(s) properties. In accordance with standard operating procedures, provide documentation of all experimental results and present findings to manager and other appropriate staff. etc. | 10/20/2020 |
| 9890 | MSD Gaithersburg, MD Research Associate I BS in cellular and molecular biology, protein sciences, or related life science Exp: 1+ year(s) |
A Research Associate I (RA I) is responsible for carrying out reagent and assay development activities in the laboratory, under supervision, working to achieve development project goals including data analysis and assay qualification. This is a laboratory position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). Some degree of professional latitude, creativity and self management is expected. DUTIES AND RESPONSIBILITIES: Analyze and prepare reagent and product documentation, organize and procure reagents, perform experiments, analyze data and document results. etc. | 10/20/2020 |
| 9891 | Microbiologics St. Cloud, MN Quality Control Lab Assistant BS/BA in microbiology or related Exp: None necessary |
Responsible for assisting Quality Control (QC) department with daily, weekly, and monthly tasks while also assisting other departments. Additional duties performed as outlined below. Responsible for labware: Preparation of labware to be autoclaved. Sterility testing. Residue checking of washed labware. Wash labware when necessary. Daily, weekly, and monthly maintenance of the laboratory equipment. Setting up QC organisms. Taking inventory and ordering of supplies. Cleaning and maintaining lab equipment, i.e. staining station, pH meter, VITEK. etc. | 10/20/2020 |
| 9892 | MRI Global Gaithersburg, MD Chemist MS in chemistry, forensic science, or equivalent Exp: Not necessary for MS candidates |
MRIGlobal is seeking a highly motivated chemist to join our chemistry program in the Physical Sciences Group. The position will involve providing analytical and logistic support for US Government clients requiring characterization of unknown samples. The position will require the use of a variety of techniques for the identification of unknown materials and impurities/degradants (e.g., GC-MS, LC-MS, DART-MS, Raman, FTIR, XRF, etc.). The chemist may also be responsible for instrument calibration and maintenance, data processing and review, and assisting with drafting monthly or final reports. etc. | 10/20/2020 |
| 9893 | MRI Global Kansas City, MO Microbiologist MS in biology, microbiology, molecular biology, or equivalent Exp: Not necessary for MS candidates |
MRIGlobal currently has an exciting opportunity for an Associate Scientist with emphasis in Microbiology and Molecular Biology for our Life Sciences Center in Kansas City, Missouri. With minimal supervision, this position will perform technically-based tasks and laboratory experimentation related to microbiology and molecular biology applications according to established protocols and SOPs. The individual will execute research project procedures, perform data analysis, and write summary reports. Typical methods include bacterial and viral culturing, nucleic acid extraction and PCR techniques. The individual will be responsible for proficiency in the use of all equipment and procedures for the assigned area with strict adherence to quality control and quality assurance assessments. etc. | 10/20/2020 |
| 9894 | Millipore Sigma Milwaukee, WI Distribution Associate 2 HS diploma or equivalent Exp: 1+ year(s) |
The Distribution Associate role plays a critical role in the fulfillment of customer orders through the activities of receiving, picking, packing, and shipping of life science materials. Standing for long periods of time, operating powered industrial equipment and lifting up to 50lbs frequently. etc. | 10/20/2020 |
| 9895 | Millipore Sigma St. Louis, MO Associate Scientist - QC Enzymes BS/AS in chemistry, biology, chemical engineering, or related life science Exp: 1+ year(s) (AS); 0 years (BS) |
At MilliporeSigma the Associate Scientist will evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department. Safely perform operations, ensuring quality expectations are met throughout the process. Perform routine assays, processes and/or unit operations. Complete the volume of work required to achieve group/departmental goals and meet deadlines. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). Communicate the status of operations and bring deviations to the attention of supervisor. Provide complete and accurate records consistent with quality guidelines. Ensure all applicable logbooks have been filled out completely as required by current procedures. Interact with other departments as needed. etc. | 10/20/2020 |
| 9896 | Miltenyi Biotec San Jose, CA Manufacturing Associate BS in a biological science Exp: 1-3 year(s) |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. Overall, your keen ability to carry out key cell processing and manufacturing procedures will champion the continued development of Miltenyi Biotec products and growing success. etc. | 10/20/2020 |
| 9897 | Miltenyi Biotec Waltham, MA Molecular Biology Research Associate - Next Generation Sequencing BS in chemistry, molecular biology, biochemistry, or related Exp: 1 year |
As a member of the Miltenyi Biotec Next Generation Sequencing (NGS) team, you will be responsible for preparing sequencing chemistry reagents for the NGS team and help with instrument set up and runs. Additionally, you will work collaboratively with the leads of the amplification, nucleotide and chemistry teams, preparing sequencing chemistry reagents for experiments in the Waltham lab, organize reagent shipments to internal teams, and set-up and run sequencing instruments. As a result of your close collaboration and expertise in preparing sequencing chemistry agents, you will support the continued success of Miltenyi Biotec as a whole. etc. | 10/20/2020 |
| 9898 | Minnetronix Medical St. Paul, MN Software Engineer I BS in computer science, software engineering, or similar Exp: 0-3 years |
As a Software Engineer I at Minnetronix, you’ll design, implement and test real-time embedded medical device software and supporting applications and prototypes. Working under close engineering supervision on a cross-functional team, you’ll help bring medical devices from concept through development and into production . We have a broad client base so project assignments will span an array of products, be broad in nature, and require creativity and ingenuity. Essential Duties and Responsibilities: Assist in definition, analysis and allocation of requirements. Implement source code that meets product requirements in compliance with applicable coding standards. Contribute to analysis, review and evaluation of design alternatives and failure mode analyses. Assist in the creation and document ation of module-level software architecture and all aspects of software design. Unit test source code using IDE’s, debuggers, emulators, communication analyzers, scopes, and logic analyzers. Install, qualify, and configure development tools and utilities. etc. | 10/20/2020 |
| 9899 | Minnetronix Medical St. Paul, MN Software Technician I AS/AA Exp: 1-4 year(s) |
As a Software Technician I at Minnetronix, you’ll assist in the development or manufacture of products, fixtures, or prototypes while supporting the creation of new Class II/III medical devices. Working with project leaders, engineers, and other technicians, you’ll provide software engineering support. This may comprise building, testing, and qualifying tools, fixtures and prototype assemblies that include software and hardware and performing other tasks as needed. You will be expected to contribute to the team while enhancing your own technical expertise and increasing your responsibilities. We have a broad client base so project assignments will span an array of products of moderate complexity, be broad in nature, and require creativity and innovation towards self-determined, self-directed solutions. Job Duties and Responsibilities: Work in compliance with the Minnetronix Quality Management System. Embedded design support. Software tool creation, qualification, maintenance, use, and support potentially including, but not limited to: Work with software engineers to determine SW tool needs. Create and/or assimilate tools as needed. etc. | 10/20/2020 |
| 9900 | Miromatix Eden Prairie, MN R&D Operations Technician -Temporary Position HS diploma or equivalent Exp: 1-2 year(s) |
Miromatrix has an immediate opening for a highly motivated R&D Operations Technician at our Eden Prairie, MN facility. The term of the position is 6 months based upon a critical business need, with the potential to advance to a full-time role based upon performance during the term of employment. Primary duties include: Performs various support functions using proper procedures to meet cGMP cleaning requirements. Maintains and cleans equipment and the facility; maintains and restocks supplies; strong attention to detail is essential while dealing with multiple tasks. Additional cleaning (i.e., emergency cleanups, construction cleanups, and room set-ups) will need to be performed on an as needed basis. Major responsibilities are preparing, maintaining, and sterilizing supplies and equipment for use in the laboratory. etc. | 10/20/2020 |
| 9901 | Moderna Bloomington, IN Specialist / Engineer II, External Manufacturing, US MS Exp: 0-2 year(s) |
Reporting to the Senior Manager of US External Manufacturing, the Specialist/ Engineer II will be part of a team responsible for Moderna’s manufacturing activities at 3rd-party contract manufacturing organizations (CMO). Here’s What You’ll Do: Ensure operational and technology transfer activities are performed completely and compliantly at CMOs to deliver a quality product and meet Moderna requirements. Ensure externally manufactured drug products are produced and stored according to the appropriate documentation in order to obtain the required quality. Review instructions relating to external production operations and ensure their strict implementation by the CMOs. Ensure in collaboration with quality that the appropriate qualification, maintenance, trainings and validations are performed to meet the appropriate Moderna’s requirements. etc. | 10/20/2020 |
| 9902 | Moderna Norwood, MA (Contract) Manufacturing Associate I, 1st Shift BS in biology, chemistry, chemical engineering, or related Exp: Not necessary for BS candidates |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. The anticipated time frame for this assignment is six months. etc. | 10/20/2020 |
| 9903 | Moderna Norwood, MA (Contract) Manufacturing Associate I, DNA Plasmid BA/BS/AA/AS Exp: Not required |
The individual in this role will be part of a cohesive team responsible for supporting GMP DNA-based medicines for evaluation in human clinical trials focusing primarily in DNA Plasmid manufacturing. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. The anticipated time frame for this assignment is six months. etc. | 10/20/2020 |
| 9904 | Moderna Norwood, MA Research Associate/Sr. Research Associate, Process Development BS in chemical engineering, chemistry, biochemistry, or related Exp: 0-3 years |
The incumbent will collaborate closely with Moderna’s process development, analytical development, and process automation teams. The successful candidate must be able to work in a fast-paced and highly dynamic environment, will have relevant academic and or industrial experience in large molecule bioprocessing, and will be able to contribute to both process development and automation related activities. Previous experience with enzymatic reactions, chromatography, and/or tangential flow filtration is preferred. We seek applicants that are proactive, enthusiastic, and show a passion for process development. Applicants should have exceptional time management and communications skills with a strong attention to detail. etc. | 10/20/2020 |
| 9905 | Moderna Norwood, MA Technician I (Material Handler) Manufacturing, 3rd Shift HS diploma or equivalent Exp: 1+ year(s) |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will support the handling and processing of materials within manufacturing operations at the Moderna Norward facility in accordance with established processes and procedures. The successful candidate will be able to document and communicate their operational observations clearly and efficiently. They will be curious to learn and able to demonstrate a high degree of working flexibly. Here’s What You’ll Do: Safely transport product, equipment and materials (buffers, drug substance) from the warehouse to designated areas in accordance with Standard Operating Procedures (SOP) and EH&S requirements in support of the manufacture of mRNA medicines. etc. | 10/20/2020 |
| 9906 | Moderna Norwood, MA Technician I (Material Handler) Manufacturing, 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will support the handling and processing of materials within manufacturing operations at the Moderna Norward facility in accordance with established processes and procedures. The successful candidate will be able to document and communicate their operational observations clearly and efficiently. They will be curious to learn and able to demonstrate a high degree of working flexibly. Here’s What You’ll Do: Safely transport product, equipment and materials (buffers, drug substance) from the warehouse to designated areas in accordance with Standard Operating Procedures (SOP) and EH&S requirements in support of the manufacture of mRNA medicines. etc. | 10/20/2020 |
| 9907 | Moderna Norwood, MA Technician I (Material Handler) Manufacturing, 1st shift HS diploma or equivalent Exp: 1+ year(s) |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will support the handling and processing of materials within manufacturing operations at the Moderna Norward facility in accordance with established processes and procedures. The successful candidate will be able to document and communicate their operational observations clearly and efficiently. They will be curious to learn and able to demonstrate a high degree of working flexibly. Here’s What You’ll Do: Safely transport product, equipment and materials (buffers, drug substance) from the warehouse to designated areas in accordance with Standard Operating Procedures (SOP) and EH&S requirements in support of the manufacture of mRNA medicines. etc. | 10/20/2020 |
| 9908 | Minnesota Valley Testing Laboratories New Ulm, MN Inorganic Laboratory Technician AS in chemistry Exp: Not required for AS candidates |
The primary responsibilities include performing basic routine analysis in our Inorganic laboratory. Position is responsible for preparing reagents and solutions, setting up laboratory equipment and performing a variety of routine wet chemistry analysis. | 10/20/2020 |
| 9909 | Minnesota Valley Testing Laboratories New Ulm, MN Microbiology Laboratory Technician BS/BA in food science, biology, or chemistry Exp: Not required for BS/BA candidates |
Responsible for sample transfers and preparation in the Micro lab as well as completing analysis by setting-up laboratory samples and performing routine tests to determine microbial characteristics of Salmonella, E.coli, and Listeria. Performs samples for plating and operates dilutor. | 10/20/2020 |
| 9910 | Minnesota Valley Testing Laboratories New Ulm, MN Environmental Organic Laboratory Technician BS/BA in chemistry or biology Exp: Not required for BS/BA candidates |
The primary responsibilities include sample and reagent preparation, data processing and calculations through use of LIMS. Follows method and SOPs. Performs extractions on Wisconsin DRO/EPA DRO soils and waters, 608 and 8081/8082 pesticides, 8270 base/neutral acids and TCLP samples. Performs dilutions and prepares standards. Uses accelerated solvent extractor to extract appropriate soil samples. Performs maintenance on instruments. | 10/20/2020 |
| 9911 | Mylan Morgantown, WV Senior Associate, Customer Relations BS/BA Exp: 0-1 year(s) |
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help: Identify and meet U.S. customer, consumer, and HCPs needs via phone, email, or fax by clarifying issues, researching and exploring answers or alternate solutions to all inquiries within set timelines for all business units. Maintaining the CRM database by logging call details accurately in accordance with department guidelines to report various trends to senior leadership. Maintaining current thorough knowledge of all business units and product portfolios, marketing campaigns, pricing, website information, PAP programs, FAQs, and other relevant programs and information to ensure One Mylan is accurately represented as a shared service. etc. | 10/20/2020 |
| 9912 | Mylan Louisville, KY Professional Sales Representative, Respiratory BS/BA Exp: 1+ year(s) |
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help: Develops business plan for assigned territory that is consistent with Mylan’s sales plans, strategies and objectives. Conducts quality sales presentations to all targeted customers. Achieve quarterly sales goals within territory while adhering to all ethical sales practices and required regulations. Understands and demonstrates targeting principles. Develops pre-call planning strategy for key targets. etc. | 10/20/2020 |
| 9913 | Mylan Chattanooga, TN Professional Sales Representative, Respiratory BS/BA Exp: 1+ year(s) |
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help: Develops business plan for assigned territory that is consistent with Mylan’s sales plans, strategies and objectives. Conducts quality sales presentations to all targeted customers. Achieve quarterly sales goals within territory while adhering to all ethical sales practices and required regulations. Understands and demonstrates targeting principles. Develops pre-call planning strategy for key targets. etc. | 10/20/2020 |
| 9914 | Locus Biosciences Research Triangle Park, NC Research Associate BS/MS in microbiology, synthetic biology, genetic engineering, or related Exp: 6+ months |
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Research Associate. This position is well suited for those that can accomplish defined work, as well as assist in approaching and solving complex scientific problems. This individual will be responsible for assisting in the generation, production and characterization of novel antimicrobial products. The ideal candidate will be able to independently conduct general microbiological and molecular biology research, and assist in the development of our broader research goals. This individual must be able to communicate effectively in formal and informal settings and be able to work well within a team. Candidates should have prior laboratory experience and be competent at basic molecular biology techniques. etc. | 10/13/2020 |
| 9915 | Locus Biosciences Research Triangle Park, NC Data Analyst BS/MS in bioinformatics, computational biology, data science, or related Exp: 6+ months |
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Data Analyst. This individual will be responsible for assisting in the generation, production and characterization of novel antimicrobial products. Primary responsibilities include maintaining and leveraging data acquired from automated and high-throughput instruments. The ideal candidate will be able to drive the automation of data acquisition from lab instruments, maintain a data warehouse, and derive meaningful insights from large datasets. This individual must be able to communicate effectively in formal and informal settings and be able to work well within a team. Candidates should have a passion for data-driven decision making and bringing life-saving therapeutics to patients. etc. | 10/13/2020 |
| 9916 | Locus Biosciences Research Triangle Park, NC Translational Medicine Research Technician BS/BA Exp: 1-5 year(s) |
Locus Biosciences is seeking highly motivated applicants to join our research and development team as a full-time Research Technician within the Translational Medicine group. This position is well-suited for highly motivated technicians that have a desire to push product development forward into critical preclinical in vitro and in vivo testing across a variety of therapeutic indications. This individual will work directly with scientists in both Development Translational Medicine as well as the Discovery group to develop and execute in vivo animal models and analyze tissue samples using various molecular and biochemical assays. The ideal candidate will be well organized and have a scientific background as well as experience with microbiology techniques and in running animal models. Candidates must have the ability to manage multiple concurrent projects, but be flexible, adjusting plans as the data dictate. The individual must be able to communicate effectively and be able to work across interdisciplinary teams. etc. | 10/13/2020 |
| 9917 | LogicBio Therapeutics Lexington, MA Research Associate/Senior Research Associate, Vector Development and Operations BS in engineering, biotechnology, biology, or related science Exp: 1-3 year(s) |
LogicBio is seeking a highly motivated and scientifically rigorous individual to join our Vector Development and Operations group at either the Research Associate or Senior Research Associate level. This position will focus on developing research vector production methods, vector analytical methods and producing pre-clinical material. Primary Responsibilities: Manufactures research grade rAAV vectors utilizing suspension cell culture in shaker flasks. Executes processes for purification of rAAV utilizing various techniques such as depth filtration, centrifugation, column chromatography and TFF. Performs occasionally analytical tests such as qPCR/ddPCR, SDS-PAGE, infectivity assays. Fills out batch records, and accurately completes documentation associated with preclinical manufacturing. etc. | 10/13/2020 |
| 9918 | LGC Petaluma, CA Quality Control Technician I, Swing Shift BS in chemistry, chemical engineering, pharmaceutical sciences, or related Exp: 1+ year(s) |
The Quality Control Technician I focuses on the performance of analytical testing activities within the QC Chemistry lab. They are responsible for testing intermediate and finished chemical products, analysing the results of Quality Control testing and comparing results to established specification and customer requirements. In addition, they perform testing and/or review of incoming goods. This position reports to the Quality Control Supervisor/Quality Control Manager. Areas of Responsibility: Completing analytical Quality Control activities for chemical products in accordance with established procedures. Ensuring products tested adhere to established specifications and customer requirements for product release. etc. | 10/13/2020 |
| 9919 | LGC Novato, CA GMP Manufacturing Technician I - Formulation BS/BA Exp: Not necessary for BS/BA candidates |
The GMP Manufacturing Technician I position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. Areas of Responsibility: To perform this job successfully, an individual must be able to perform each essential function satisfactorily. Essential Functions: Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director. Maintain batch records, equipment logs and other production records as directed per company procedures. Maintain a clean an orderly laboratory environment. etc. | 10/13/2020 |
| 9920 | Lumenis Salt Lake City, UT Test Technician AS/AA in laser/electro optics Exp: 1-2 year(s) |
We are seeking a highly motivated, positive and bright Technician to join our small company atmosphere with opportunities to learn and grow. This would be a rewarding, challenging and fun opportunity for the right person. Primary Function: Responsible for performing the set-up, calibration, testing, troubleshooting of circuits, components, instruments, optical and mechanical assemblies. Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams. Tests and troubleshoots assemblies and Laser systems. etc. | 10/13/2020 |
| 9921 | Luminex Austin, TX Assembly Associate I, Consumables - Limited Assignment (2nd Shift) - US AS/AA in technical electronics or a mechanical field Exp: 1+ year(s) |
The Assembly Associate I, Consumables will be responsible for: Building of cassettes for use by Engineering, Development, Clinical Studies, and product sales. Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System. Providing feedback on the processes to assure continuous improvement by noting differences in parts, assemblies, tools, fixtures, or process steps. What you will do: Coordinate with other assembly associates daily in support of integration testing, manual instruction development and production process development. All to support a quality process. Hands-on assembly, test and troubleshooting of system builds and re-work. etc. | 10/13/2020 |
| 9922 | Luminex Madison, WI Manufacturing Associate I, Reagents - US AS in chemistry, life sciences, biotechnology, medical technology or related Exp: 1+ year(s) |
Delivering manufacturing requirements against production schedule within a focused manufacturing operation and/or product segment. Work schedule may include alternate shifts. Participating in manufacturing processes to support new product design transfer, stability program, process development, equipment validations, process validations and investigations and resolution of product/process issues. Performing maintenance and calibration of Manufacturing measuring and monitoring devices as well as maintaining the integrity of work areas. What you will do: Deliver manufacturing requirements and attainment of production schedule for standard inventory, build-to-order, and contract manufacture market products. Deliver manufacturing requirements for qualification/processing of incoming materials, production intermediates, and stability samples. Deliver timely and accurate completion of manufacturing sections of process documentation and related business system transactions. etc. | 10/13/2020 |
| 9923 | Luminex Austin, TX Assembly Associate I, Consumables - Limited Assignment US (3rd Shift) AS/AA in technical electronics or a mechanical field Exp: 1+ year(s) |
The Assembly Associate I, Consumables will be responsible for: Building of cassettes for use by Engineering, Development, Clinical Studies, and product sales. Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System. Providing feedback on the processes to assure continuous improvement by noting differences in parts, assemblies, tools, fixtures, or process steps. What you will do: Coordinate with other assembly associates daily in support of integration testing, manual instruction development and production process development. All to support a quality process. Hands-on assembly, test and troubleshooting of system builds and re-work. etc. | 10/13/2020 |
| 9924 | Luminex Austin, TX Assembly Associate I, Consumables - Limited Assignment - US (1st Shift) AS/AA in technical electronics or a mechanical field Exp: 1+ year(s) |
The Assembly Associate I, Consumables will be responsible for: Building of cassettes for use by Engineering, Development, Clinical Studies, and product sales. Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System. Providing feedback on the processes to assure continuous improvement by noting differences in parts, assemblies, tools, fixtures, or process steps. What you will do: Coordinate with other assembly associates daily in support of integration testing, manual instruction development and production process development. All to support a quality process. Hands-on assembly, test and troubleshooting of system builds and re-work. etc. | 10/13/2020 |
| 9925 | Lundbeck Bothell, WA Quality Control Associate BS/BA Exp: 0-2 years |
Lundbeck is seeking a Quality Control Associate to support QC testing activities for projects in both the early and late stage of clinical and commercial development. The ideal candidate is detail oriented, organized and will have some experience in a Quality Control or other scientific laboratory or setting. ESSENTIAL FUNCTIONS: QC Sample Shipping and Sample Management. Coordinate and track sample shipments between various departments at Lundbeck and multiple CMOs/contract testing labs including international shipments. Lead a weekly multi-departmental sample shipping working group meeting. Proactively communicate shipping timelines from contract testing labs to other QC personnel and other Lundbeck contacts, as required. etc. | 10/13/2020 |
| 9926 | Lygos Berkeley, CA Down Stream Processing: Lab Technician/Research Associate BS Exp: 0-3 years |
Lygos is seeking a Lab Technician/Research Associate candidate to set up, run, clean, and support downstream processing experiments. The successful candidate will have experience with general lab procedures, data interpretation and reporting in a fast paced and dynamic work environment. The candidate will work under the supervision of the Production Specialist. The candidate will be expected to work collaboratively with other team members within DSP (Down Stream Processing) and other departments including molecular biology, downstream processing, and analytical. The Lygos team works closely with all employees to support career development and facilitate the learning of new skill sets. etc. | 10/13/2020 |
| 9927 | LSNE Bedford, NH QA Associate I - Document Control BS/BA Exp: 1 year |
Manage, coordinate, and maintain CGMP documentation, procedures, and records to ensure only controlled copies are reviewed, approved, issued, distributed, and archived. JOB DUTIES: Maintain Document Change Request/Quality System event databases and Master Documents/List. Maintain Designated Satellite Areas for controlled paper based record management system. Facilitate Client Batch Record Creation/Modifications/Approvals. Issue, maintain and archive Controlled Documentation/Batch Records/Testing Data Sheets/Equipment Log Books/Quality System event documents and Logs. Track and facilitate Periodic SOP reviews. Manage Record/Document Filing system. Proof and edit document changes, as necessary. Assist in client audit preparation and reconciliation. Other duties as assigned. etc. | 10/13/2020 |
| 9928 | MabPlex San Diego, CA Process Development Engineer/Associate MS Exp: 1+ year(s) |
This is an intermediate experienced engineer/associate position that will play an important role in developing stable cell lines and robust cell culture processes to be used in clinical manufacturing. Experience will dictate the exact title. The position will report to the Manager of Cell Line Development. Essential Job Responsibilities: Develop stable cell lines: Host cell transfection with target plasmid. Minipool screening and single-cell cloning. Shake flask fed-batch studies to support stability studies and top clone selection. etc. | 10/13/2020 |
| 9929 | Mallinckrodt Pharmaceuticals St. Louis, MO Chemistry Technician III BS in chemistry, biology, or related Exp: 1-3 year(s) |
Job Description Summary: Develop and produce pharmaceutical products via multiple methodologies, follow standard operating procedures, maintain compliance with Good Manufacturing Practices. ESSENTIAL FUNCTIONS: cGMP Active Pharmaceutical Ingredient (API) manufacturing. Conduct lab and pilot scale chemistry methods to synthesize and produce pharmaceuticals. Maintain strict FDA and cGMP compliance. Routinely and effectively maintain laboratory and supplies. Be able to troubleshoot and resolve technical issues along with comprehensive knowledge of hand tools. Follow Six Sigma and Lean manufacturing methods for stream lining and quality production. etc. | 10/13/2020 |
| 9930 | Mallinckrodt Pharmaceuticals Hobart, NY Packaging Operator I HS diploma or equivalent Exp: 3-6 months |
Packaging Line Operator is responsible for tending machines and conveyors at various stages of the packaging line to maintain efficient, continuous packaging of the product for shipment. Essential Functions: Components are in Place and Filled. Sets up assigned station(s) on the line including assembly of basic equipment and preparing materials needed (e.g. bottles, caps, cotton, etc.). Tends/operates station(s) during production run to insure proper operation and keep station filled with supplies or product. Weighs product at various stages of the packaging process. Performs checks/tests required for applicable station(s). Adjusts containers/materials for proper placement and remove defective pieces. Starts and stops equipment when required. Performs hand-packaging and material-handling functions. etc. | 10/13/2020 |
| 9931 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - 4on/4off C Shift 6pm-6am HS diploma or equivalent Exp: 3-6 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 10/13/2020 |
| 9932 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - 4on/4off D Shift 6pm-6am HS diploma or equivalent Exp: 3-6 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 10/13/2020 |
| 9933 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - 4on/4off A Shift 6am-6pm HS diploma or equivalent Exp: 3-6 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 10/13/2020 |
| 9934 | Mallinckrodt Pharmaceuticals Raleigh, NC Quality Tech II BS in a physical science or related Exp: 1-3 year(s) |
The Quality Tech II analyzes process samples as received and performs non-routine analysis as requested. She/he will analyze finished goods and raw materials by chemical, physical, and instrumental means to ensure quality as needed. Must be able to work a 12 hour shift schedule of (7pm-7am) rotating shift with potential of night shift. In addition to occasional overtime as needed. ESSENTIAL FUNCTIONS: Performs in process testing for internal customers. Performs finished goods, returned goods, and stability testing for external customers as needed. Performs specified analysis on all process controls samples and reports in a timely manner by telephone or computer entry using approved written procedures and proper laboratory techniques. etc. | 10/13/2020 |
| 9935 | Mallinckrodt Pharmaceuticals Hobart, NY Manufacturing Assoc I - 1st Shift HS diploma or equivalent Exp: 3-6 months |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 10/13/2020 |
| 9936 | Marker Therapeutics Houston, TX Quality Control Specialist MS in a biological science, biotechnology, or related Exp: 1 year |
The Quality Control Specialist will join a newly formed Quality Control team and report directly to Quality Control Manager. This position would give you the opportunity to be part of the brand-new Quality Control (QC) Cell Therapy Laboratory and be a key figure in day-to-day operations. The specialist will assist and collaborate with R&D on a successful transfer of analytical methods to QC. In addition to that, the QC Specialist will be performing assays in support of production, product release and stability studies on Marker’s GMP products and drug components, in accordance to the Quality Control Standard Operating Procedure and in compliance to FDA regulations. etc. | 10/13/2020 |
| 9937 | Masy Bioservices Pepperell, MA Biorepository Operations Technician I HS diploma or equivalent Exp: 1-2 year(s) |
This position is responsible for storage of customer products requiring specific environmental conditions. Duties involve cleaning, couriering, shipping, receiving and inventorying. Abide by area work instructions to ensure customer product is stored appropriately and moves to/from customer and to/from Masy with appropriate controls. Accuracy, attention to detail and GMP compliance are key requirements. Duties/Responsibilities: Store product appropriately and enter information electronically into applicable system. Maintain and monitor temperature in chambers during addition and removal of product. Understand temperature and time as they relate to customer storage needs. Clean and maintain the Biorepository facility and chambers. etc. | 10/13/2020 |
| 9938 | Maze Therapeutics South San Francisco, CA Research Associate II / Senior Research Associate, Stem Cell Biology (Contract) MS Exp: Not necessary for MS candidates |
We are seeking a talented and highly motivated researcher with experience in molecular and cellular biology to contribute to projects developing stem cell models for drug discovery for a variety of therapeutic areas. The successful candidate will have a thorough understanding of molecular biology with familiarity in human pluripotent stem cells (hiPSCs/hESCs). Additional experience with CRISPR gene editing, assay development, and high throughput screening is preferred. As a member of the stem cell group, you will work alongside stem cell scientists to support the growth of new differentiations, assays, and screens. This is an exciting interdisciplinary role in a dynamic cross-functional team that will contribute directly to the identification of new targets and the design and validation of novel disease-modifying therapeutics. etc. | 10/13/2020 |
| 9939 | Medicomp Washington, DC Entry Level Cardiac Medical Device Sales Position - DC, VA and WV BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 9940 | Medicomp Seattle, WA Entry Level Medical Device Sales Person -Seattle BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 9941 | Medicomp San Francisco, CA Entry Level Medical Device Sales Person - NorCal BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 9942 | Medicomp New York, NY Entry Level Cardiac Medical Device Sales Position - New York BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 9943 | Medicomp Fort Lauderdale, FL Entry Level Cardiac Medical Device Sales Person - South Florida BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 9944 | Medicomp Cleveland, OH Entry Level Cardiac Medical Device Sales Position - Michigan and Ohio BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 9945 | Medicomp Melbourne, FL Digital Marketing Associate BS/BA in business, marketing, communications, or related Exp: 0-2 years |
The role of Digital Marketing Associate will be to manage Medicomp’s presence in the digital universe. This will include Facebook, LinkedIn, PPC advertising, drip campaigns, and CRM management. As the Digital Marketing Associate, you will have the opportunity to hone your SEO and advertising skills alongside a talented team of internal professionals and external consultants who live and breathe marketing. You should have a passion for digital marketing and excel at both technical- and analytical-related tasks, in addition to bringing creativity to the role. You will have a direct impact on driving lead acquisition and management efforts for our sales team by helping to execute both on our marketing plan and advertising campaigns. etc. | 10/13/2020 |
| 9946 | Cantel Medical Rochester, NY Distribution Specialist - 1st Shift AS/AA Exp: 1 year |
The Specialist, Distribution is a functional role that includes distribution order picking, stocking, packaging, and other material handling and inventory control tasks to ensure timely and accurate shipments are made to our customers using various indicators or signals. To assure team continuity across all warehouse operations, this position may also be required to learn, perform, and or be certified to assist within other areas of Warehouse Operations including material & inventory, traffic, or others as assigned. The role works collaboratively with key business partners to ensure timeliness of execution, appropriate safeguards to protect during transit, and or other. Interacting with Customer Service, Purchasing, Planning, Operations and Material Control to identify and meet business requirements. etc. | 10/13/2020 |
| 9947 | Cantel Medical Rochester, NY Manufacturing Support Operator HS diploma or equivalent Exp: 1-5 year(s) |
This position exists as a support to the manufacturing department. This position labels and delivers all packaging with the correct lot information and ensure that each production team member has the materials that they need to ensure maximum productivity and uptime. What you will do: Label all inner packaging with correct lot information for each machine in operation on a given shift. Apply labels to outer and intermediate packaging for all products on a given shift. Deliver materials as required to each machine in operation on a given shift. Empty the trash and scrap generated from the production cell over the course of a given shift. Assist the team lead with material movement inside the department, including raw materials, finished goods, and WIP materials. etc. | 10/13/2020 |
| 9948 | Cantel Medical Rochester, NY Manufacturing Support Operator - 3rd Shift HS diploma or equivalent Exp: 1-5 year(s) |
This position exists as a support to the manufacturing department. This position labels and delivers all packaging with the correct lot information and ensure that each production team member has the materials that they need to ensure maximum productivity and uptime. What you will do: Label all inner packaging with correct lot information for each machine in operation on a given shift. Apply labels to outer and intermediate packaging for all products on a given shift. Deliver materials as required to each machine in operation on a given shift. Empty the trash and scrap generated from the production cell over the course of a given shift. Assist the team lead with material movement inside the department, including raw materials, finished goods, and WIP materials. etc. | 10/13/2020 |
| 9949 | Cantel Medical Rochester, NY Manufacturing Support Operator - 2nd Shift HS diploma or equivalent Exp: 1-5 year(s) |
This position exists as a support to the manufacturing department. This position labels and delivers all packaging with the correct lot information and ensure that each production team member has the materials that they need to ensure maximum productivity and uptime. What you will do: Label all inner packaging with correct lot information for each machine in operation on a given shift. Apply labels to outer and intermediate packaging for all products on a given shift. Deliver materials as required to each machine in operation on a given shift. Empty the trash and scrap generated from the production cell over the course of a given shift. Assist the team lead with material movement inside the department, including raw materials, finished goods, and WIP materials. etc. | 10/13/2020 |
| 9950 | Medpace Denver, CO Entry PC- Imaging Services BS in a health science or engineering Exp: Entry level |
Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based Imaging Project Coordinator to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities: Compile and maintain project-specific status reports and project timelines associated with imaging studies; Maintain inventory of imaging supplies for study sites; and Interact with study sites and internal associates. etc. | 10/13/2020 |
| 9951 | Merck Durham, NC Associate Specialist, Environmental Monitoring BS Exp: 1+ year(s) |
At least 1 year of relevant post-degree work experience in Environmental Monitoring, Aseptic Manufacturing or Microbiological Laboratory Operations. Evidence of good oral and written communication skills ( i.e., effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills). Attention to detail, flexibility and an awareness of production and attendant quality control problems. Basic understanding of GMPs and of regulatory requirements as they apply to the vaccine, sterile pharmaceutical or related fields. Ability to sit, stand and move within work-space for extended periods, ability to perform repetitive tasks including frequent hand to finger manipulations, grasping pushing and pulling; ability to lift up to 50 pounds. etc. | 10/13/2020 |
| 9952 | Merck San Francisco, CA Entry Level Field Sales Representative - Women's Health (San Francisco, CA South) BA/BS Exp: Entry level |
The Women’s Health Customer Representative supports customers by providing clinical information on our Company's products, as well as education, clinical training programs, and resources. They do this to support customer needs in an effort to help the provider or system meet the goals of their patients. The Women’s Health Customer Representative is the primary point of contact for a variety of customers within their assigned geography. These customers may include: health care providers such as physicians, nurses, pharmacists as well as quality directors, LARC initiative personnel and office managers. Within their geography there are a diverse set of health care locations that they will call upon in order to execute their role including: clinics, health departments, integrated delivery systems, and hospitals. etc. | 10/13/2020 |
| 9953 | Meridian Bioscience Cincinnati, OH Senior Research Associate MS Exp: 1 year |
The immunoassay function within R&D is responsible for developing the next generation diagnostic kits for Meridian. The Senior Research Associate will support the development of a new diagnostic device as part of an assay team. Responsible for designing and executing experiments, acquiring data, drawing conclusions for discussion and recommendations. Key Duties: Supports the technical work of a project – execute experiments. Participates in brainstorming discussions and sharing ideas with the team. Presentations – present data during team meetings. etc. | 10/13/2020 |
| 9954 | Columbia University Irvington, NY Technician B BS Chem, Bio, Physics, related Exp: 0 yrs |
The Center for Radiological Research is seeking a technician to work with scientists studying the health hazards and antimicrobial efficacy of ultraviolet light. They will gain experience in immunohistochemistry, animal handling and husbandry, and ultraviolet exposure techniques. The primary work location will be at the Radiological Research Accelerator Facility at the Columbia University Nevis Laboratories in Irvington, NY. Occasional work at the Columbia University Irving Medical Center may be required. | 10/02/20 |
| 9955 | KBI Biopharma The Woodlands, TX Manufacturing Support Associate I HS diploma/AS/AA Exp: 0+ year(s) |
The Manufacturing Support Associate I is designed as an introduction to the environment of GMP manufacturing. This position performs all routine / non routine cleanings of the GMP facilities, Process Waste, and continuously supports the manufacturing operations. This position requires a shift schedule. Aseptic and Gowning qualifications are required for this position. Must be able to document and maintain records to comply with regulatory requirements, cGMP’s, Policy Documents and SOP’s. Maintain Manufacturing facility with routine and non routine cleaning. Clean, Operate and Maintain Process Waste Area. Prepare, build and complete processing assemblies (PAR) for production. Completes Facilities response forms and ensures communication to inform other departments requiring EM sampling if required. etc. | 10/4/2020 |
| 9956 | KBI Biopharma Durham, NC Research Associate BS/MS in chemistry, biochemistry, or related Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. etc. | 10/4/2020 |
| 9957 | KBI Biopharma Durham, NC Research Associate I/II - Analytical Development BS/MS in chemistry, biochemistry, or related Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. etc. | 10/4/2020 |
| 9958 | KBI Biopharma Durham, NC Manufacturing Associate I/II, Downstream (Days) BS/BA Exp: 0+ year(s) |
Job Summary: Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products at high quality levels. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP's and batch records. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. | 10/4/2020 |
| 9959 | KBI Biopharma Durham, NC Manufacturing Associate/Sr. Manufacturing Associate-Downstream (day shift) BS/BA Exp: 0+ year(s) |
Job Summary: Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products at high quality levels. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP's and batch records. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. | 10/4/2020 |
| 9960 | KBI Biopharma Durham, NC Manufacturing Associate/Sr. Manufacturing Associate-Upstream (night Shift) BS/BA Exp: 0+ year(s) |
Responsible for a wide variety of cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Follow SOPs, perform daily tasks in a clean-room, retain records and write reports. May also be responsible for troubleshooting. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP’s and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation. Follow specific techniques and operations while demonstrating an understanding of cGMPs and how they apply to specific responsibilities. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. | 10/4/2020 |
| 9961 | KBI Biopharma Durham, NC Research Associate/Sr. Research Associate BS/BA Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. etc. | 10/4/2020 |
| 9962 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst I, Pharma Services BS/BA in chemistry, biochemistry, or related Exp: 1+ year(s) |
The Analyst I is responsible for preparation of reagents and solutions as well as sample processing under required regulatory documentation. Analyzes data, interprets results, and contributes to troubleshooting activities, such inventory of chemicals, washing glassware, waste disposal and/or general cleanup. May provide basic training for other laboratory personnel. Process and/or analyze samples. Prepare and label laboratory solutions. Perform and/or verify calculations related to reagent preparation and/or sample analysis. Conduct sample inventory and verify sample identities. Review information and documentation for accuracy. Prepare study records for archive. Independently create basic experiment plans. etc. | 10/4/2020 |
| 9963 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Laboratory Maintenance Technician BS/BA Exp: 1 year |
The Lab Maintenance Technician I performs maintenance, testing, troubleshooting, calibration and repair on support and laboratory systems. May also analyze data, interpret results or contribute to troubleshooting activities. Works on assignments that are moderately complex in nature in which judgment is required in resolving problems and making routine recommendations. ESSENTIAL FUNCTIONS: Process new and/or retired equipment. Perform calibration, repair, and preventive maintenance on support systems and laboratory equipment. Perform and/or verify calculations related to calibration and/or maintenance events. Review information and documentation for accuracy. Support the recertification of support systems and laboratory equipment. Supports activities of the Operations Department, as assigned. etc. | 10/4/2020 |
| 9964 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst II, Pharma Services BS/BA in chemistry, biochemistry, or related Exp: 1+ year(s) |
The Analyst II is responsible for preparation of reagents and solutions as well as sample processing under required regulatory documentation. Analyzes data, interprets results, and contributes to troubleshooting activities, such inventory of chemicals, washing glassware, waste disposal and/or general cleanup. May provide basic training for other laboratory personnel. Process and/or analyze samples. Prepare and label laboratory solutions. Perform and/or verify calculations related to reagent preparation and/or sample analysis. Conduct sample inventory and verify sample identities. Review information and documentation for accuracy. Prepare study records for archive. Independently create basic experiment plans. Process and summarize data using applicable software. etc. | 10/4/2020 |
| 9965 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst II, Pharma Dose Formulation Analysis BS in chemistry, biochemistry, biology or related Exp: 1-2 year(s) |
Responsible for preparation of reagents and solutions as well as sample processing under required regulatory documentation. Analyzes data, interprets results, and contributes to troubleshooting activities, such inventory of chemicals, washing glassware, waste disposal and/or general cleanup. May provide basic training for other laboratory personnel. Key Job Responsibilities: Typical responsibilities of the Analyst II may include, but are not limited to, the following: Process and/or analyze samples. Prepare and label laboratory solutions. Perform and/or verify calculations related to reagent preparation and/or sample analysis. Conduct sample inventory and verify sample identities. etc. | 10/4/2020 |
| 9966 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Report Analyst I HS diploma or equivalent Exp: Entry level |
Provide administrative support related to writing reports, test procedures, filing, and preparation of studies for archival. Works on assignments that are complex in nature in which considerable judgment and initiative are required in resolving problems and making recommendations. ESSENTIAL FUNCTIONS: Works in conjunction with Management/PSI and Quality to ensure report writing process is accurate and completed in a timely manner. Provides support for creation of reports, tables, and transmittals to be published by Management/PSI. Prepares studies for archival based on scientific department requirements. etc. | 10/4/2020 |
| 9967 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst I, Pharma Discovery BS/AS in chemistry, biochemistry, or related Exp: Entry level |
Depending on prior experience, the Analyst I will be responsible for sample preparation/extraction, preparation of reagents and solutions under required regulatory documentation, analysis of data, interpretation of results, contributing to troubleshooting activities, performing chemical inventory, and general laboratory activities such as washing glassware, waste disposal and/or general cleanup. Once fully trained, the Analyst may provide basic training for other laboratory personnel. With demonstrated progress and initiative, the candidate will also have opportunities for learning value added skills. Key Job Responsibilities: Typical responsibilities may include, but are not limited to, the following: Process and/or analyze samples of various biological matrices. Prepare and label laboratory solutions or buffers. etc. | 10/4/2020 |
| 9968 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst II, Pharma LC-MS/MS (2nd Shift) BS/BA in chemistry, biochemistry, or related Exp: Not necessary for BS/BA candidates |
The Analyst II will be responsible to help extend our active hours by working a 2nd shift. Primary duties are preparation of reagents and solutions under required regulatory documentation, initiating and finishing sample analysis, monitoring results, contributing to troubleshooting activities. Other duties may include performing chemical inventory, and general laboratory activities such as washing glassware, waste disposal and/or general cleanup. With demonstrated progress and initiative, the candidate will also have opportunities for learning other value-added skills. Key Job Responsibilities: Typical responsibilities may include, but are not limited to, the following: Prepare and label laboratory solutions or buffers. Perform and/or verify calculations related to reagent preparation and/or sample analysis. etc. | 10/4/2020 |
| 9969 | Kite Santa Monica, CA Process Engineer, Process Technology and Materials Development MS/MA Exp: 0+ year(s) |
As a Process Engineer I, you will be responsible for designing and executing engineering activities and lab studies in support of process automation, technology development, technology evaluation, equipment qualification, process validation, and GMP manufacturing. Additional responsibilities include analyzing and presenting experimental results, drafting / reviewing protocols, production procedures, and technical reports including documentation for regulatory filings. You will work within the process technology and materials development team to design and scale-out cell therapy processes, evaluate new materials, implement innovative solutions, and support or improve existing technologies to advance Kite’s product portfolio. You will work closely with analytical, process design, validation, manufacturing sciences, operations, business strategy, and external collaborators as needed to achieve the above objectives. etc. | 10/4/2020 |
| 9970 | Kite Emeryville, CA Senior Research Associate – In Vivo Unspecified Exp: 1-5 year(s) |
The in vivo pharmacology group is seeking an experienced and motivated Research Associate to join the growing team in Kite Emeryville. The candidate will join an established group, playing a key role in generating in vivo data in support of multiple programs utilizing engineered human T cells with chimeric antigen receptors (CARs). Responsibilities will include, but are not limited to: Perform in vivo studies to evaluate the efficacy of engineered T cells in mouse tumor models. Establish tumor models through SQ or IV inoculation, administer T cells IV, and dose mice with multiple agents IP or PO. Monitor in-life study measurements (tumor volume/burden, body weight), and enter data in associated software programs. etc. | 10/4/2020 |
| 9971 | Kite Santa Monica, CA Research Associate, Process Design BS in biochemical engineering, chemical engineering, or related Exp: 1+ year(s) |
As a Research Associate in Process Design, you will provide process development support for New INDs, technology transfers, process validations and GMP manufacturing for Kite’s engineered autologous T cell therapy products. Additionally, you will draft and review protocols, production procedures, and process development reports. You will work with the Process Development team to design and scale-out cell therapy processes, manage equipment qualification and support process validation, as well as draft documentation for regulatory filings to advance Kite’s product portfolio. Key responsibilities: Hands on execute and collaborate on process design laboratory studies to support process development, optimization and characterization and essential process improvements. Perform hands on work in a cell culture lab and process training for GMP clinical production. etc. | 10/4/2020 |
| 9972 | Krystal Biotech Pittsburgh, PA GMP Manufacturing Associate BS/BA Exp: 1+ year(s) |
Krystal Biotech, Inc is seeking a highly motivated and dynamic GMP Manufacturing Associate to support launch of and manufacturing at our Pittsburgh GMP facility. The ideal candidate will have foundation experience in upstream and/or downstream biologics or gene therapy manufacturing. Responsibilities will include, but are not limited to, the following: Develop and execute SOPs. Execute and report IQ/OQ for equipment. Operate and maintain manufacturing equipment. Perform process for manufacturing drug product for clinical trials. Clean and maintain GMP facility. Engage with process development team for tech transfer of improvements/scale up. etc. | 10/4/2020 |
| 9973 | KSQ Therapeutics Cambridge, MA Scientist/Sr Scientist, Pharmacology MS Exp: 1-3+ year(s) |
KSQ Therapeutics, Inc. is seeking an exceptional and highly motivated Senior Associate Scientist/Scientist to join the Pharmacology group. The successful applicant will contribute to in vivo pharmacology efforts to support the advancement of our pre-clinical Oncology and Immuno-Oncology small and large molecule pipeline. This is a unique opportunity to learn and develop in a highly dynamic and interdisciplinary environment. Responsibilities: Independently execute on a wide variety of in vivo techniques across multiple projects with delivery of high quality data. Work collaboratively within department and across departments to effectively achieve project goals and timelines. Work enthusiastically as part of an interdisciplinary team. etc. | 10/4/2020 |
| 9974 | KVK Tech Newtown, PA Packaging Supervisor AS/BS Exp: 1-3 year(s) |
Lead, train, and direct the daily activities of the Packaging/Manufacturing Departments by following all applicable Standard Operating Procedures/cGMP’s as well as maintain a safe work environment. Key Duties & Responsibilities: Supervise day to day operations of Manufacturing/Packaging. Assist with daily planning and scheduling to ensure proper workflow. Monitor, organize, and execute all functions associated with packaging of pharmaceutical commercial products and assuring compliance with cGMP, SOP, FDA, DEA, and OSHA rules and regulations. Work directly with management and group leaders to ensure appropriate follow through of the weekly planning schedule. etc. | 10/4/2020 |
| 9975 | KVK Tech Newtown, PA Sample Management Associate AS/BS in a laboratory science Exp: None needed |
Sample Management Associate provides support to Sample Coordinator and performs administrative tasks in the Sample Management Department. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. JOB RESPONSIBILITIES: Performs duties and training to acquire the skills required for sample and standard handling in support of the laboratory. Handling of samples received in Quality Control Laboratory. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. Quality Control related tasks like receiving, documenting, distributing and reconciliation of all samples received in the laboratory. etc. | 10/4/2020 |
| 9976 | KVK Tech Newtown, PA Manufacturing Operator HS diploma or equivalent Exp: 1-3 year(s) |
Operators are responsible for operating special purpose machines or industrial equipment to specifications on production basis in typical oral solid dose pharmaceutical manufacturing. Processes include dispensing and weighing of materials, using automatic and semi-automatic equipment for tablet manufacturing, combining materials to make blends and solutions, and packaging of finished product. JOB RESPONSIBILITIES: Ensure the proper set-up and operation of standard pharmaceutical process equipment such as Granulators, Blenders, Mills, Tablet Presses, Tablet Coaters and Packaging. etc. | 10/4/2020 |
| 9977 | KVK Tech Langhorne, PA Quality Control Microbiologist BS in microbiology or related Exp: 1 year |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensure their delivery in an accurate and timely manner following proper safety precautions. Also provide QC microbiology support to the Aseptic Manufacturing and validation process. DUTIES & RESPONSIBILITIES: Familiar with Drug Regulations, Pharmacopeia’s and Regulatory requirements. Authoring SOP’s and Test Methods when required. Assurance of cGMP and GLP compliance in the QC Microbiology Laboratory. Responsible for laboratory cleanliness and biohazard removal. etc. | 10/4/2020 |
| 9978 | KVK Tech Newtown, PA QC Document Reviewer BS in chemistry or related Exp: 1+ year(s) |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. JOB RESPONSIBILITIES: Daily activities include review of documentation generated during method development, method validation, stability testing, routine testing and other analyses. The individual will interface with their supervisor, the analytical groups and QA on a daily basis. etc. | 10/4/2020 |
| 9979 | KVK Tech Newtown, PA Analytical Chemist BS/MS Exp: 1-4+ year(s) |
Perform analytical testing of raw materials, in-process materials, stability samples, finished products and product development products using different analytical techniques. JOB RESPONSIBILITIES: Operation, Calibration, Qualification, Preventive maintenance and routine trouble shooting of analytical instruments like UPLC, HPLC, GC, AAS, UV spectrophotometer, Dissolution apparatus, Laser Diffraction Particle Size analyzer, etc. Evaluate existing, develop and validate new analytical methods of drug products and drug substance as per FDA, USP and ICH guidelines by different analytical techniques. Document all performed analysis as per cGMP, USFDA and 21CFR211.194 guidelines. Follow cGMP (current Good Manufacturing Practices), GLP (Good Laboratory Practices), 21CFR211.22, 21CFR211.28 and 21CFR211.170. etc. | 10/4/2020 |
| 9980 | KVK Tech Newtown, PA Topical Formulation Associate MS in chemistry, biochemistry, or pharmaceutical sciences Exp: 1-3 year(s) |
Person exhibits aptitude in assisting in the development of topical product pharmaceutical formulations, as well as meeting timelines for the department. JOB RESPONSIBILITIES: Assist in the development of broad range of topical product pharmaceutical formulations including gels, creams, solutions and ointments. Develop pharmaceutical formulations utilizing Quality by Design (QbD) and risk assessment concepts. Contribute and support the analytical efforts and interpretation of data generated from experimental batches. Write technical documents to support regulatory submissions and technical transfers. Interact cross departmentally and provide technical guidance to achieve company objectives. etc. | 10/4/2020 |
| 9981 | Lab Connect Johnson City, TN Jr. Project Analyst BS/BA in accounting, finance, economics, business administration, or related Exp: 0-3 year(s) |
To provide financial support to the Senior Analyst and Project Manager as assigned. The mission of the position is to support the accurate reporting of the financial position of each project internally. Essential Functions (including but not limited to): Responsible for project set-up in an ERP system, client billing support, and other financial aspects of assigned projects. Assist in financial support to ensure the operational effectiveness of the project. Maintain all project data in the ERP system and on Sharepoint. Prepare reporting and financial analysis for the Finance team and issue findings and variances to plan. Identify and highlight potential issues related to project financial risks that impact company profitability. etc. | 10/5/2020 |
| 9982 | Lab Connect Johnson City, TN Proposal Associate - Remote Opportunity BS/BA in science, business, or marketing Exp: 1-5 year(s) |
The following duties are normal for this position; however, they are not to be construed as exclusive or all-inclusive. Other duties may be required and assigned. Essential Duties and Other Responsibilities: Prepare quotations for protocols, bid requests, study revisions, and additions’ using the company’s pricing tools. Complete budget to actual reconciliations at predetermined time points over the course of awarded studies. Assist in making recommendations on desirable proposals based on established financial and operational criteria, as required. etc. | 10/5/2020 |
| 9983 | Lampire Biological Laboratories Ottsville, PA Large Animal Technician Animal science degree Exp: Not necessary for degree candidates |
Care of animals including feeding, cleaning, treatment and preventive medicine. Daily production and maintaining the animal areas of the facility. Responsibilities Include (but are not limited to): Animal care AM/PM daily. Complete daily production which may include injections, bleeding, milking etc. Maintain animal living areas. Document findings and job completions in the required logs. etc. | 10/5/2020 |
| 9984 | Lampire Biological Laboratories Everett, PA Small Animal Technician HS diploma/BS in a life science Exp: 1 year |
The primary responsibility of this individual is to maintain the overall health and well-being of the rabbits including cage and facility maintenance. This would include the feeding and watering of rabbits, administering treatments, as well as swapping, cleaning, disinfecting, and sanitizing all animal housing units and animal facilities. Responsibilities Include (but are not limited to): Feeding, watering, and administering treatments, including observing and reporting any signs of disease/illness and help to treat minor cases of such findings. Scraping, chipping, and dusting, animal caging units. Swapping/rotating animal. Caging units. Disassembling/assembling, cleaning, disinfecting, and sanitizing all animal caging units including feeders, water bottles, and enrichment items. etc. | 10/5/2020 |
| 9985 | Lampire Biological Laboratories Everett, PA Purification Technician BS Exp: Not necessary for BS candidates |
This position will be responsible for the purification of antibodies at the Everett facility. Responsibilities Include (but are not limited to): Routine buffer preparation for all processes being performed in the department. Protein A and Protein G purification of Normal igGs and other antibodies. Write and revise Standard Operating Procedures (SOP’s) and Batch Records (BR) as needed. Assist in filing, labeling and finished product good inspection. Operate basic Laboratory and Analytical equipment. Compliance with all Standard Operating Procedures (SOP’s) in relation to Protein Purification. etc. | 10/5/2020 |
| 9986 | Lannett Seymour, IN Drug Product and Stability Chemist I - 1st Shift BS in chemistry or related Exp: Not necessary for BS candidates |
This position is primarily responsible for the laboratory testing of in-process, release and stability samples for commercial drug products. Work on a team of 6 or more analysts. No direct reports. No purchase approval or budget responsibilities. Responsibilities: Perform accurate and timely analysis of in-process, release and stability samples for drug products according to current analytical procedures, SOPs, laboratory guidelines and safety requirements. Testing performed to include basic lab equipment and procedures, such as pH, Assay by HPLC, and Dissolution. Document all laboratory testing and maintain accurate and legible notebooks and records. Peer review of data, reports and notebooks. etc. | 10/5/2020 |
| 9987 | Latham Biopharm Group Elkridge, MD Associate / Senior Associate / Consultant, Quality Assurance BS/BA Exp: 1-2 year(s) |
The ideal candidate must be able to work independently and have excellent interpersonal relationship skills with flexibility to adapt to fast pace environment with changing priorities. Job Duties: Provide consulting services for LBG client including, but not limited to: Evaluation and disposition of materials with the assurance that the materials were produced in conformance to all applicable policies/procedures of the Company's compliance with all governing regulations. Coordinate and/or support the preparation of procedures, processes and quality improvements. Assists in the coordination of significant quality events including fact-finding, investigation support, coordination of clinical quarantine and recovery actions. Collaboration with clients and vendors to ensure robust processing and continuous improvement. etc. | 10/5/2020 |
| 9988 | LeMaitre Vascular Burlington, MA Quality Inspector - Non Exempt (Hourly) Position HS diploma Exp: 1-3 year(s) |
Complete in-process, final inspection of medical devices and review DHR and record QC Chemistry and Microbiology results. Responsibilities: Read work instructions to complete in-process and final inspections. Use a wide assortment of QC inspection instruments to assure components and devices are manufactured and are functioning in accordance to specifications. Use simple test equipment and record data and interpret its pass/fail status. etc. | 10/5/2020 |
| 9989 | LeMaitre Vascular Burlington, MA Manufacturing Technician - Non Exempt (Hourly) Position HS diploma Exp: 1-3 year(s) |
The Manufacturing Technician is responsible for carefully following manufacturing instructions and adhering to applicable company quality standards and requirements to ensure the proper manufacturing of our collagen vascular graft. Responsibilities: Manufacture vascular graft products as required to support all customer, internal, clinical, and other demand. Package vascular grafts as required as per current process specifications. Maintain timely and accurate documentation of all manufacturing activities, including but not limited to device history records and inventory counts. Complete scheduled production runs in an efficient, timely manner to meet schedules. Participate in Continuous Improvement projects or events as requested. Assist with inventory counting activities as required. etc. | 10/5/2020 |
| 9990 | Lifecore Chaska, MN Machine Operator I HS diploma or equivalent Exp: 6+ months |
The Machine Operator I is responsible for the setup and operation of standard packaging machinery in the packaging department. This includes working with and monitoring other packaging personnel to complete equipment set up and operation required by the department schedule. Machine Operators must comply with regulatory requirements, Good Manufacturing Practices (GMP), Standard Operating Procedures (SOP), and Manufacturing Process Records (MPR). They will perform all processes as required to fill, label, print, tray seal, pouch, final package, and inspect any Lifecore product; document completed work during packaging of final product; continually practice proper precautions and procedures when working with equipment and handling chemicals; participate in the review of batch records, procedures, and practices to help ensure the safety of all Lifecore products as well as personnel; identify and communicate quality issues to supervisor; acquire and maintain cleanroom and gowning qualification as required. etc. | 10/5/2020 |
| 9991 | LifeSensors Malvern, PA Entry Level Scientist BS/MS in the biological sciences or related Exp: 0-2 year(s) |
We are seeking individuals who are passionate about research, bring out of the box thinking and take bold steps to develop innovative technologies with applications in the ubiquitin research field. Successful candidates will have basic knowledge of biochemistry and molecular biology techniques, in particular experience with protein expression and purification and cloning. Knowledge of the ubiquitin proteasome pathway is desired. etc. | 10/5/2020 |
| 9992 | Ligand Durham, NC Associate Scientist - Molecular Biology BS/MS in cellular or molecular biology or related Exp: 0-2 year(s) |
Icagen’s facility in Durham, North Carolina currently has an opening for a talented scientist to join our Molecular Biology team. This is a full-time, laboratory-based position offering an opportunity to play key roles in identifying novel drug candidates and advancing drug development projects. The ideal candidate will have experience in a broad set of cellular and molecular biology techniques with a fundamental understanding of molecular biology. The successful candidate will be capable of managing multiple projects simultaneously while working as part of a core team. The work will be fast-paced and process-oriented in a dynamic environment which is predicated upon continuous improvement where everyone is encouraged to contribute to improving laboratory efficiency. etc. | 10/5/2020 |
| 9993 | Lipocine Salt Lake City, UT Associate Scientist BS/MS in a life science, chemical engineering, or related Exp: 1-3 year(s) |
Associate scientist needed in the area of pharmaceutical drug delivery research. Responsibilities include conducting laboratory experiments in support of formulation and process development. Qualified candidates will possess a BS/MS in life Science, chemical engineering or related field or 1-3 years experience in a pharmaceutical or chemistry laboratory. Knowledge of laboratory practices and demonstrated skills in analytical instrumental techniques (e.g. HPLC) are preferred. Excellent communication skills needed for preparing and following standard test methods and reporting experimental results. | 10/5/2020 |
| 9994 | Liquidia Morrisville, NC Contract - Associate Engineer or Senior Associate Engineer MS in engineering or technical discipline Exp: 0-1 year(s) |
The Associate Engineer / Senior Associate Engineer works within cross-functional teams to develop processes for the manufacturing of novel particles for engineered drug delivery. Specific Duties, Activities, and Responsibilities: Work with team of engineers and technicians to manufacture materials to support preclinical and clinical R&D projects. Serve as manufacturing representative for one or more R&D project teams to assist in process development activities to ensure adequate material supplies to meet project objectives. Support R&D project teams through the use of process engineering tool such process mapping, Cause and Effect Diagrams, pFMEA and basic Six Sigma tools. Assist project teams in the transition for lab scale to commercial scale manufacturing. etc. | 10/5/2020 |
| 9995 | Hologic San Diego, CA Scientist 1 R&D MS in molecular biology, chemistry, biochemistry, or related Exp: 1-3 year(s) |
Hologic is seeking a Scientist 1 responsible for initiating, directing and executing scientific research and/or development strategies. Essential Duties and Responsibilities: The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Responsible for a sub-project within the overall project goals. Understands the sub-project goals within the context of the overall project. Independently designs and performs complex experiments, analyzes data and prepares reports for the sub-project in support of the overall project. May be asked to supervise daily work of junior level employees as preparation for a management role at the next level. Demonstrated competence in one or more of the following areas: Core Services – e.g. Microbiology skills, bioinformatics, sequencing, cloning, analytical chemistry, oligo synthesis and/or purification. etc. | 9/27/2020 |
| 9996 | Hovione , NJ Process Engineer BS in chemical or other engineering or chemistry or other science Exp: 1-3 year(s) |
At Hovione, a Process Engineer's job mission is to ensure the best process engineering knowledge is applied in scaling up chemical and spray drying projects to maximize customer satisfaction ad Hovione's interests and in compliance with all Federal, State, Local and internal policies. It also includes the development of process engineering technical skills to increase the knowledge and offering on the best and state of the art technologies used in the industry. You will be responsible for: Plan and design manufacturing processes based on chemical procedures to run safely and effectively in a pilot plant/kilo lab in accordance with best known practices ensuring cGMP compliance. Contribute to the Process Hazard Analysis (PHA) of all processes under his/her responsibility and assure that all identified hazards are addressed prior to performing any activities within operations. Plan and design methods to improve efficiency in production. etc. | 9/27/2020 |
| 9997 | Humacyte Research Triangle Park, NC Process Engineer I (MSAT) BS in engineering or related Exp: 0-2 years |
Position will support the development and execution of product lifecycle management and process analytics activities. This role will work closely with personnel in Process Development, Manufacturing, Engineering, Quality Assurance, and Quality Control. Primary Responsibilities: Support execution and development of the manufacturing control strategy and Process Analytics program. Acquire, analyze, and report data trends using graphical and statistical methods. Support technology transfer and process validation of products into commercial manufacturing. Author standard operating procedures, reports, and protocols. etc. | 9/27/2020 |
| 9998 | Humacyte Research Triangle Park, NC Cell R&D Associate MS in cell biology, biochemistry, chemical engineering, mechanical engineering, or related Exp: 1-2 year(s) |
KEY RESPONSIBILITIES: Responsible for culture of primary human cells for purposes of cell expansion, characterization, and tissue engineering. Perform qRT-PCR to screen donor cells. Aseptic compounding and aliquoting media and buffers. Construct, launch and maintain bioreactors that are used to grow engineered vascular tissues. Perform cell-based assays. Verify process data, protocols, and manage supporting documents. Additional duties will include support of routine lab activities, equipment management, lab maintenance, preparation of experimental materials and protocols, and ensuring good documentation practices for all activities performed. Schedule flexibility required for some occasional cell culture activities needed outside of standard weekday business hours (e.g. weekend cell culture maintenance activities). etc. | 9/27/2020 |
| 9999 | ICU Medical Salt Lake City, UT Equipment Operator I HS diploma or equivalent Exp: 0-1 year(s) |
A Equipment Operator I is responsible for the safe and efficient operation of simple automated assembly machines. This individual will ensure the continued operation of assembly machines through interpretation of and appropriate response to machine faults and through infrequent alignment of stations and fixtures. This individual will perform simple, repetitive tasks associated with machine operation and will operate machines that require a low level of attentiveness. The operator is also responsible for ensuring that medical devices are assembled with the highest quality possible. Essential Duties & Responsibilities: Keep work area and equipment clean. Able to read and understand procedures. Responsible for safe operation of equipment in accordance with Company standards and procedures. etc. | 9/27/2020 |
| 10000 | ICU Medical Salt Lake City, UT Technician, Setup HS diploma or equivalent Exp: 1+ year(s) |
The Setup Technician supports the Production operation by setting tools and turn over to production ready for startup. The Setup Technician is required to participate in daily meetings to ensure job accuracy and priorities. Essential Duties & Responsibilities: Train with the Senior Process Technician. Train on Robotics and End of Arm Setup. Assure GMP’s, safety standards and procedures are followed per company policies. Responsible for reviewing crossover priorities and schedule with supervisor each morning. Working from molding crossover, obtain all required elements for priority job including documentation. Verify full last shot and samples of any cavities that were blocked from tool work order packet are collected, verify this represents all cavities and then have Process Tech shut down press. etc. | 9/27/2020 |
| 10001 | ICU Medical Salt Lake City, UT Associate Maintenance Technician, Molding HS diploma or equivalent Exp: 0-2 years |
The Associate Molding Maintenance Technician is required to assist in the diagnose and repair of Molding Presses and all ancillary equipment. In addition, they must be able to communicate effectively with their customer, Production, and all support groups. Finally, they are required to accurately document the work performed which is crucial and required in achieving World Class Maintenance. Essential Duties & Responsibilities: Support preventive maintenance and daily repair of injection molding presses, and auxiliary equipment. Participate with set up reduction improvements of specific injection molding presses, molds and auxiliary equipment (conveyors, dryers, thermolators, etc.) through Kaizen improvement activities. Troubleshoot pneumatic, mechanical, hydraulic and electronic and/or combined systems on Injection Molding Machines and support equipment. etc. | 9/27/2020 |
| 10002 | ICU Medical Salt Lake City, UT Service and Repair Technician AS/AA Exp: 0-2 years |
The Service Hub Technician is responsible for triaging devices where critical decisions are made on the PCI, repair, updating of service record, tracking labor and material as well as updating and printing of a Service Report that is returned with the repaired device. This person must interpret and edit the repair results into device tracking system (Oracle) so that the complaint is addressed, results are technically accurate and include all required elements ensuring that the customer understands the analysis/repair activity. Communicates with other Repair Technicians as required to clarify repair results. Essential Duties & Responsibilities: Will perform routine and complex work related to the repair and refurbished of medical devices. Troubleshoot and analyze customer device returns to problem solve root cause issues. May perform troubleshooting and repair of devices onsite at customer location. etc. | 9/27/2020 |
| 10003 | ICU Medical Salt Lake City, UT Quality Inspector I AS/AA Exp: 6 months |
Independently performs inspections on parts, materials, and supplies received from vendors, perform in-process production inspections, and ensure products comply with quality standards prior to shipment. Issues acceptance or rejection tags based on outcome of inspections, checking with supervisor on more difficult determinations. Familiar with manufacturing environment, inspecting, testing, sampling, and sorting of products / goods being manufactured. Essential Duties & Responsibilities: Audit and monitor quality requirements in accordance with company quality assurances policies and customer specifications. Conduct inspections at First Article, in-process, in-coming and completes the final inspections. Perform accurate mechanical, physical and visual inspections of raw materials, components, and sub-assemblies as per inspection plans and specification requirements. etc. | 9/27/2020 |
| 10004 | Idexx Elmhurst, IL Histology Laboratory Tech AS/BS/MS Exp: 1+ year(s) |
Histologists at IDEXX perform dissection, grossing, embedding, microtomy, special staining, and complex tissue diagnostics on veterinary samples from dogs, cats, birds, reptiles, and all other pets big and small. Are you looking to make a difference in the lives of pets? The pet owner counts on it! Who should reach out? If you have specific experience in dissection, embedding, cutting, grossing or special stains. Complex Tissue a PLUS. If you desire a role as a coordinator, lab tech, leader or trainer - you will be a contributor to a team focused on operational excellence and the sharing of best practices, our team of laboratory professionals are dedicated, driven and results-oriented. This is a laboratory, so there is potential exposure to biohazards, agents known to cause zoonotic diseases, and hazardous chemicals. etc. | 9/27/2020 |
| 10005 | Idexx Memphis, TN Histology Laboratory Technician - Days AS/BS/MS Exp: 1+ year(s) |
Histologists at IDEXX perform dissection, grossing, embedding, microtomy, special staining, and complex tissue diagnostics on veterinary samples from dogs, cats, birds, reptiles, and all other pets big and small. Are you looking to make a difference in the lives of pets? The pet owner counts on it! Who should reach out? If you have specific experience in dissection, embedding, cutting, grossing or special stains. Complex Tissue a PLUS. If you desire a role as a coordinator, lab tech, leader or trainer - you will be a contributor to a team focused on operational excellence and the sharing of best practices, our team of laboratory professionals are dedicated, driven and results-oriented. This is a laboratory, so there is potential exposure to biohazards, agents known to cause zoonotic diseases, and hazardous chemicals. etc. | 9/27/2020 |
| 10006 | iFyber Ithaca, NY Research Technician BS in the biological sciences Exp: 1 year |
iFyber is seeking a research technician to assist with R&D projects at the interface between chemistry, biology, and material science. iFyber serves clients in the regenerative medicine, medical device, diagnostics, and antimicrobial industries. The person in this position will support a variety of programs that will require experience and/or the ability to pick up bench skills related to microbiology and chemistry. Duties and Responsibilities: Conduct experimental tasks both independently. Follow established protocols and work with senior staff to adapt or design new protocols. Document information in laboratory notebooks and MS Word, Excel, and PowerPoint. Report results via verbal, written, and graphical communication. etc. | 9/27/2020 |
| 10007 | Immucor Nocross, GA Production Support Technician HS diploma or equivalent Exp: 1-3 month(s) |
We are seeking a Production Support Technician I to provide day-to-day operations support for all manufacturing areas. Our ideal candidate must be able to adapt to changes in the daily/weekly schedule to ensure customer demands are met. This position's schedule is Tuesday – Friday from 10am – 8:30pm (shift may vary to meet business needs). Additional responsibilities include: Perform washroom activities, staging and set up bottles for production use and maintain inventory. Assemble bottle preparation, manifold assembly and other components for manufacturing use. Responsible for training on all procedures assigned, and has the ability to be cross trained to assist in other production areas or departments as needed. etc. | 9/27/2020 |
| 10008 | Integer Plymouth, MN Associate Prototype Technician AS/BS Exp: 0-3 years |
The primary purpose of this role is to perform assembly and inspection operations over a range of new products and/or processes. Will support non-cyclical work which may include prototypes and pre-production lots in preparation for validation, clinical trials or transfers. Will also support multiple builds within the facility including lab and cleanroom environments. With guidance from Engineering on projects and using work procedures, this role provides support to the Engineering teams to meet various deadlines. May provide support to other team members or provide input to the Engineers on assembly, processes, and build/quality documentation. etc. | 9/27/2020 |
| 10009 | Integer Brooklyn Park, MN Manufacturing Team Member HS diploma or equivalent Exp: 1+ year(s) |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Adheres to Integer's Values, Behavioral Based Safety process and Integer Associate Quality Policy. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. etc. | 9/27/2020 |
| 10010 | Integrated DNA Technologies Coralville, IA Lab Technician II (Scientific Manuf.) BS in a science-related field Exp: Not necessary for BS candidates |
Integrated DNA Technologies, Inc. (IDT) is in the business of moving science forward. We are scientists working for scientists. Our innovative tools and solutions for genomics applications are breaking down barriers and inspiring others to dream big and achieve breakthroughs. Every lab has its own responsibilities and plays a crucial part in IDT’s success. Our entry-level scientific lab-based positions are split between three sub-titles, Synthesis, Purification, and Formulation. More detailed descriptions of each can be found below: The Technician II (Synthesis) synthesizes custom oligonucleotides according to the customer’s order. This generally includes synthesis, cleavage, deprotection and QC sampling of the products being made. The Technician II (Purification) purifies custom oligonucleotides according to the customer’s order. This generally includes the sorting, purification, and QC sampling of the products being made. The Technician II (Formulation) formulates custom oligonucleotides according to the customer’s specifications. This generally includes quantification, final packaging, and QC sampling of the products being made. etc. | 9/27/2020 |
| 10011 | Intellia Therapeutics Cambridge, MA Process Engineer, AAV Process Development MS in biochemical engineering, molecular biology, or virology Exp: 1-2 year(s) |
Intellia is seeking a skilled and motivated Process Engineer to support AAV process development in the Technical Operations group. The ideal applicant will be experienced and capable in HEK suspension culture and transfection optimization for AAV production. The position requires development, optimization and scale up of AAV production in bioreactors as well as a good understanding of viral production analytics and purification technologies. Experience with documentation and technical transfer to GMP manufacturing is a plus. Responsibilities: AAV upstream process development and transfection optimization. Develop and perform pre-clinical scale up production processes based on QbD. Collaborative integration within Tech Ops and with R&D and Automation groups. etc. | 9/27/2020 |
| 10012 | Invenra Madison, WI (Senior) Research Associate - Innovation BS/MS in the biological sciences Exp: 1+ year(s) |
Invenra is seeking an enthusiastic and creative Research Associate or Senior Research Associate with a strong background in molecular biology and protein engineering techniques. This individual will have the freedom to explore new technologies and innovations that can revolutionize Invenra’s current platforms. As part of the Innovation group, the successful applicant will work as part of a team that seeks to improve the efficiency or quality of immune-oncology drug discovery. Details of the job include cutting-edge library construction, recombinant protein expression, developing and optimizing various display strategies, and protein binding experiments. The position requires excellent scientific and problem-solving skills, creative thinking, the ability to try new things, and an enthusiasm for science. etc. | 9/27/2020 |
| 10013 | Invenra Madison, WI Research Associate - Cell Biology BS in molecular and cell biology, immunology, or other biological science Exp: 1+ year(s) |
Invenra is seeking a highly motivated Research Associate with a strong background in cellular biology. This individual will support the Invenra antibody discovery platform. Aspects of the job entail mammalian cell culture and assays, analytical flow cytometry, ELISAs, and immunofluorescence/luminescence assays. In addition, the position will involve general ordering and stocking of lab supplies as well as upkeep of standard cell biology equipment (i.e. incubators, biosafety cabinets, etc.). The position requires strong communication and organizational skills as well as attention to detail. etc. | 9/27/2020 |
| 10014 | Invitae San Francisco, CA Lab Automation Support Engineer BS/BA in a laboratory discipline Exp: 1+ year(s) |
At Invitae, we have highly automated labs that process samples 7 days a week. To sustain volume growth and maintain high caliber instrument reliability, we are hiring an Automation Support Engineer to join the operations team. The key responsibility of the Automation Support Engineer is to provide support to the clinical lab automation and processes. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multiple tasks, and prioritize time sensitive tasks. What you will do: Provide prompt troubleshooting support to laboratory operations and escalate situations as needed to subject matter experts in, computing, automation, and laboratory processing. Support laboratory processes by troubleshooting errors related, but not limited to laboratory robotics and LIMS communication. etc. | 9/27/2020 |
| 10015 | Invitae San Francisco, CA DNA Extraction Technician BS in clinical laboratory studies or related Exp: 1+ year(s) |
We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work at our San Francisco location as well as ability to work overtime and off-schedule days as needed. etc. | 9/27/2020 |
| 10016 | Invitae San Francisco, CA Data Analyst, Lab Operations Background in life sciences Exp: 1+ year(s) |
We are seeking a data analyst to join our team. Responsibilities will include monitoring our product pipeline using custom software tools with the goal of assuring samples move through smoothly. Candidates should have experience with UNIX. They are expected to take initiative to automate tasks and troubleshoot the production process through detail-oriented analysis. An important part of this job is to be able to clearly communicate technical findings to non-technical teammates. etc. | 9/27/2020 |
| 10017 | Stryker Saginaw, MI Trauma Sales Associate BS/BA Exp: 1+ year(s) |
What you will do: You will get exposure to the proven winning Stryker Trauma culture that delivers Industry leading results in all market segments. You will receive best-in-class formal Trauma training on product portfolio and selling skills which includes on-the-job training in the operating room. You’ll become an expert on surgical procedures by observing well-over 300 cases in your first year. You will develop well-rounded field exposure to prepare you in all aspects of the selling/ servicing process when a territory opportunity arises. You will develop a high level of competency in Orthopaedic surgical needs and procedures becoming a valuable member of the surgical team and positively impacting surgical outcomes. etc. | 9/27/2020 |
| 10018 | Stryker Tucson, AZ Trauma Sales Associate BS/BA Exp: 1+ year(s) |
What you will do: You will get exposure to the proven winning Stryker Trauma culture that delivers Industry leading results in all market segments. You will receive best-in-class formal Trauma training on product portfolio and selling skills which includes on-the-job training in the operating room. You’ll become an expert on surgical procedures by observing well-over 300 cases in your first year. You will develop well-rounded field exposure to prepare you in all aspects of the selling/ servicing process when a territory opportunity arises. You will develop a high level of competency in Orthopaedic surgical needs and procedures becoming a valuable member of the surgical team and positively impacting surgical outcomes. etc. | 9/27/2020 |
| 10019 | Stryker San Antonio, TX CMF Associate Sales Representative BS/BA Exp: 1+ year(s) |
At Stryker’s Craniomaxillofacial (CMF) division: You’ll work closely with experienced Sales Representatives and Managers to build your knowledge, skill and comfort with clinical and product knowledge as well as selling styles and techniques. They will serve as your coaches and mentors to share lessons learned for how to build and grow a successful business. You’ll receive training and be expected to study and prepare independently to perform at the highest levels in the operating room, working amongst surgeons and healthcare professionals. The expectations are challenging, yet rewarding. You’ll represent Stryker as a leader in our industry and the marketplace. You’ll have the opportunity to identify and promote solutions and sell products that change our patient’s lives. etc. | 9/27/2020 |
| 10020 | Ionis Carlsbad, CA Scientist, Manufacturing BS/MS in chemical engineering Exp: New graduates |
We are seeking a motivated and versatile individual to join our Manufacturing group in an individual contributor, bench Scientist position. The successful candidate will work closely with other scientists in an interdisciplinary team environment to help optimize our solid-phase oligonucleotide manufacturing process, to make improvements to the synthesis of small molecules that make up our supply chain, and to aid in analytical investigations. The candidate should possess a strong work ethic, excellent communication skills, and a demonstrated record of success in a chemical laboratory setting. RESPONSIBILITIES: Optimize manufacturing and purification processes for the solid-phase synthesis of oligonucleotides and oligonucleotide conjugates. Investigate raw material and process-related impurities. etc. | 9/27/2020 |
| 10021 | Janssen Research Development San Diego, CA Associate Scientist, Discovery Chemistry MS in synthetic organic or mechanical chemistry Exp: 1+ year(s) |
We are seeking an experienced Bachelor’s- or Master’s-level medicinal chemist with excellent organic synthesis expertise to advance small molecule drug discovery programs toward the clinic. In this laboratory-based position, the successful candidate will partner with both internal and external medicinal chemistry teams to generate innovative solutions to synthetic and medicinal chemistry challenges within the context of small molecule drug discovery projects. She/he will maintain close interactions with computer assisted design scientists and biologists. Strong people skills and the ability to thrive in a team and goal driven environment are key attributes. This individual must also excel in communication and have strong interpersonal skills necessary to influence in a collaborative multidisciplinary environment. etc. | 9/27/2020 |
| 10022 | Just - Evoted Biologics Redmond, WA Associate Scientist, High Throughput Analytical BS in biochemistry, molecular biology, chemical engineering, chemistry or related Exp: 0-5 years |
Just is seeking a motivated and creative Associate Scientist, who desires a significant opportunity to improve worldwide access to biotherapeutics. We are looking for a motivated scientist to join a fast-paced, collaborative, and multidisciplinary team. As a member of the High Throughput Analytical group, you will support process development through application of H/UPLC and CE methodologies. Additional experience with other analytical techniques as well liquid handling robotics is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. etc. | 9/28/2020 |
| 10023 | Just - Evoted Biologics Seattle , WA Associate Scientist, Process Development BS in biochemistry, molecular biology, chemical engineering, chemistry or related Exp: 0-3 years |
Just.Bio is seeking motivated and creative Associate Scientists, who desire a significant opportunity to improve worldwide access to biotherapeutics. We are looking for team members to join a fast-paced, collaborative, and multidisciplinary group to support process development for low-cost biotherapeutic manufacturing. The successful candidates will have some experience in one or more of the following areas including chromatography, filtration, electrophoresis, analytical chemistry, cell culture and/or bioreactor operations. Experience with high throughput, robotic techniques for analytical testing, chromatography, and/or protein expression, as well as statistical design of experiments and/or process modeling, is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. etc. | 9/28/2020 |
| 10024 | Just - Evoted Biologics Redmond, WA Commissioning, Qualification & Validation Engineer I/II – Manufacturing Technical Operations BS in engineering science or related Exp: 1+ year(s) |
Just is seeking a highly motivated Commissioning, Qualification & Validation Engineer that desires a significant opportunity to improve worldwide access to biotherapeutics. The primary focus of this job is to lead the process equipment and utilities commissioning, qualification and validation activities required for late-stage clinical and commercial biologics manufacturing. This comprises all phases of implementation, including ownership of key deliverables such as risk assessments, user requirements specifications, functional and design specifications. The selected candidate will also be responsible for commissioning and qualification protocol generation and execution as well as validation summary reports. Additional job responsibilities will include periodic review and requalification of validated equipment and systems to verify compliance with appropriate regulations and maintaining required change control procedures and impact assessments. etc. | 9/28/2020 |
| 10025 | Just - Evoted Biologics Redmond, WA Manufacturing Associate – Cell Culture AS/BS in science or engineering Exp: 1+ year(s) |
Just-Evotec Biologics is seeking a highly motivated Cell Culture Manufacturing Associate that desires a significant opportunity to improve worldwide access to biotherapeutics. This team member will be responsible for the manufacture of mammalian cell-based biotherapeutics for clinical use under cGMP conditions. Manufacturing Associates are initially expected to execute commissioning and validation activities in addition to other start-up support activities. Post start-up activities, the associates are expected to execute process recipes, monitor equipment and processes, perform basic tasks, including sampling, and routine maintenance of lab equipment. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures and manufacturing documentation. etc. | 9/28/2020 |
| 10026 | Just - Evoted Biologics Seattle , WA Process Engineer I – Purification BS in a biological or engineering science Exp: 0-3 years |
Just is seeking a highly motivated entry-level manufacturing Process Engineer that desires a significant opportunity to improve worldwide access to biotherapeutics. This team member will be responsible for the manufacture of mammalian cell-based biotherapeutics for clinical use under cGMP conditions. Under direct/moderate supervision, job responsibilities include set-up, operation, and maintenance of disposable-based manufacturing equipment; execution of manufacturing process operations; and assisting in general lab operations. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures, and manufacturing documentation. etc. | 9/28/2020 |
| 10027 | Just - Evoted Biologics Redmond, WA Process Engineer I/II, Downstream – Manufacturing Technical Operations BS in engineering science or related Exp: 1-3 year(s) |
Just is seeking a highly motivated Process Engineer in the Manufacturing Technical Operations group that desires a significant opportunity to improve worldwide access to biotherapeutics. The primary focus of this job is to support the startup of a first-of-its-kind flexible and reconfigurable cGMP manufacturing facility. The selected candidate will be responsible for supporting the procurement, commissioning, and testing of the process equipment for the new facility, including developing commissioning documentation and standard operating procedures. In addition, the candidate will be responsible for supporting process engineering activities for the new manufacturing plant, including process transfer / tech transfer for clinical and commercial biologics manufacturing, writing technical documentation within cGMP compliant systems, troubleshooting equipment, and introducing new manufacturing technologies such as continuous processing. etc. | 9/28/2020 |
| 10028 | Just - Evoted Biologics Redmond, WA Process Engineer I/II, Modeling – Manufacturing Technical Operations BS/MS in chemical or biochemical engineering Exp: 0-2 years |
Just is seeking a highly motivated process engineer in the Manufacturing Technical Operations group that desires a significant opportunity to improve worldwide access to biotherapeutics. The primary focus of this job is to develop mathematical modeling and simulation tools for clinical and commercial biologics manufacturing, data analysis and visualization, empirical and numerical algorithm development, and conveyance of modeling insights through written reports and presentations. The selected candidate will also be responsible for performing bioprocess modeling, writing and revising computer programs, and generating technical reports or documentation. In addition, this team member will gain an understanding of new manufacturing technologies and equipment, including disposable-based systems and continuous processing technologies for a first-of-its-kind flexible and reconfigurable cGMP manufacturing facility. etc. | 9/28/2020 |
| 10029 | Karius Redwood City, CA Research Associate BS/MS in biology, molecular biology, genetics, or related Exp: 1-3 year(s) |
As a Research Associate you will work alongside scientific leaders in NGS-based infectious disease diagnostics providing meaningful contributions to making an impact in the lives of patients while contributing to the company’s growth and development . You will be responsible for maintaining process excellence for a state-of-the art NGS infectious disease diagnostic assay by assisting in an established in-house manufacturing process. You will be also involved with several exciting research projects and be at the forefront of non-invasive diagnostics working alongside our scientists to deliver new products. The ideal candidate should have experience with nucleic acids, NGS, or other molecular biology assays to conduct laboratory experiments on research projects under the direction of senior lab personnel. etc. | 9/28/2020 |
| 10030 | KBI Biopharma Durham, NC Research Associate BS/MS in chemistry, biochemistry, or related Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. etc. | 9/28/2020 |
| 10031 | KBI Biopharma Durham, NC In-Process Support Associate BS in a scientific discipline Exp: 0-2 years |
KBI Biopharma, Inc. is a contract services organization committed to reducing process development time, decreasing production cost and increasing speed of development for biopharmaceuticals. We are seeking an In-Process Support Associate with strong protein chemistry background to perform cGMP in-process analytical support. These services include in-process and release testing for drug substances manufactured internally. Job Description: Execute activities according to cGMP regulations and company SOPs. Provide STAT assay coverage including 2nd shift and weekends as required by the manufacturing schedule. Assays include A280 and RP titer. Log samples or verify sample log in outside of standard business hours. etc. | 9/28/2020 |
| 10032 | KBI Biopharma Louisville, CO Research Associate - Rapid Analytics Job BS Exp: 0-2 years |
Open position available in the rapid analytics testing group. Responsible for analytical testing of client samples. Testing may include using client-based methods or some method development. Ideal candidate is able to quickly and accurately generate results. Technical writing skills are a plus. Job Requirements: Familiarity with biophysical and protein characterization techniques, such as: SV-AUC, CD, DSC, FTIR, HPLC, UV-Vis. Design and execution of experiments. Routine statistical analysis on generated data sets using JMP or equivalent statistical software. Attention to detail in documentation of experiments in electronic laboratory notebooks. etc. | 9/28/2020 |
| 10033 | KBI Biopharma Research Triangle Park, NC Research Associate I/II - Analytical Development BS/MS in chemistry, biochemistry, or related Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. etc. | 9/28/2020 |
| 10034 | KBI Biopharma Durham, NC Manufacturing Associate I/II, Downstream (Nights) BS Exp: 0+ year(s) |
Job Summary: Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products at high quality levels. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP's and batch records. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. | 9/28/2020 |
| 10035 | Fujifilm Diosynth Research Triangle Park, NC Associate Scientist, Cell Culture BS Exp: 1+ year(s) |
The Upstream Process Development group is seeking an Associate Scientist with experience in mammalian or insect cell culture technologies. An Associate Scientist assists in conducting experiments for programs and works with the team to maintain the lab and equipment. The individual monitors on going experiments and can identify unusual occurrences. An Associate Scientist understands and applies knowledge within area of expertise and can take an active role in non-routine process development activities. MAJOR ACTIVITIES AND RESPONSIBILITIES: Conducts routine laboratory experiments using established procedures and protocols. Maintains lab equipment, supplies and work area. Quality of work is complete and technically sound to ensure integrity of research. etc. | 9/21/2020 |
| 10036 | Fujifilm Diosynth Research Triangle Park, NC Process Scientist/Engineer I BS Exp: Not necessary for BS candidates |
The Process Scientist/Engineer I represents the technical operations department before FDBU customers, regulatory agencies and management. This individual will manage the new client process and ensure project objectives are completed. The Process Scientist/Engineer will also contribute to the technology transfer of multiple projects at various project life-cycle stages (clinical material to commercial supply). Additionally, this individual must possess strong process understanding to implement and execute process risk review and process/cleaning qualification and validation activities. etc. | 9/21/2020 |
| 10037 | Fujifilm Diosynth Research Triangle Park, NC Process Scientist/Engineer II MS Exp: Not necessary for MS candidates |
Responsibilities: May support technical transfer of client project in and to manufacturing as applicable. Summarizes and report data. Interacts with supervisor and reports results and interpretation of experiments, project deliverables, and process readiness. Supports capital projects by providing technical expertise. Supports new project site-fit assessments as needed. Assists in developing SOPs and engineering documents. Familiar with relevant literature. etc. | 9/21/2020 |
| 10038 | Fujifilm Diosynth Research Triangle Park, NC Scientist I, Analytical Methods Transfer MS Exp: 1+ year(s) |
The successful candidate requires the following knowledge, skills and abilities: One to three years of applicable hands on experience in Plate Based methods. Additional experience in one or more of the following fields: HPLC/UPLC, capillary electrophoresis, spectroscopy or biophysical characterization methods. Good interpersonal skills, the ability to work individually or as part of a team, and problem solving capabilities of standard laboratory techniques. Have strong oral communication skills. In addition, the successful candidate must be comfortable multi-tasking in a fast-paced environment with defined deliverables and deadlines. GMP experience a plus. etc. | 9/21/2020 |
| 10039 | Fujifilm Diosynth Research Triangle Park, NC Downstream Production Technician HS diploma/BS/BA Exp: 1+ year(s) |
Fujifilm Diosynth Biotechnologies, U.S.A., Inc. is seeking Downstream Production Technicians (all levels) to work in our Downstream Manufacturing group. The successful candidate will execute Development and Production processes as well as the accompanying documentation. This position could either be a day shift position (7:00 am – 7:00 pm) or a night shift position (7:00 pm – 7:00 am). The candidate hired will be working on day shift for the first six months for training, and then transition to the night shift. Main areas of responsibilities include: Executing development and production processes as well as process documentation. Understanding processing principles and scientific theory behind operations steps. etc. | 9/21/2020 |
| 10040 | Fujifilm Diosynth College Station, TX Assistant Scientist- AD BS in chemistry, biology, or related life science Exp: Not necessary for BS candidates |
Essential Functions: Assist in the transfer, development, and optimization of customer programs. Independent operation of instrumentation in the PD laboratories. Assist in conducting, data plotting and reporting the results of laboratory experiments. Monitor ongoing experiments for any unusual occurrences. Maintenance of lab equipment, supplies and records. Execution of basic experimental protocols. Maintaining detailed laboratory notebooks following FDBT procedures. Perform all other duties as assigned. etc. | 9/21/2020 |
| 10041 | Fujifilm Diosynth College Station, TX Associate Scientist – Analytical Method Transfer BS/MS in chemistry, biology, or related life science Exp: 1 year |
Essential Functions: Execute method transfers/qualifications/validations based on regulatory guidelines and industry best practices. Perform assays to evaluate the accuracy, precision, specificity, linearity, robustness, and detection/quantitation limits of analytical methods. Maintain laboratory instrumentation and assist with vendor qualifications. Develop expertise on a subset of analytical methods and participate in method troubleshooting activities. Maintain awareness of project timelines and milestones and openly communicate scheduling challenges. Assist in the preparation of technical documents including protocols and reports. Finalize analytical test methods; route documents for approval within Master Control. Interface with other groups to drive project success, including Analytical Development, Project Management, Quality Control, and Quality Assurance. etc. | 9/21/2020 |
| 10042 | GeneDX Gaithersburg, MD Primary Analyst I (FT, 40 Hours) MS in medical technology or related life science Exp: Not necessary for MS candidates |
Responsibilities include: Case Analysis -- Efficiently analyzes all data (ABI, NG, Exome, Exon Array, MLPA, qPCR, Genome Array, etc.) and completes all primary analysis related steps according to standard procedures. Performs at a consistent level of analysis by completing a reasonable number of analysis steps with minimal errors. Reliably identifies variants meeting confirmation criteria and sends them for confirmation using appropriate methods, as applicable. Aims to identify novel situations and seek prompt and appropriate advice on how to proceed. Makes sure all relevant aspects of a case are complete and either sends them to review or logs them out, as appropriate. etc. | 9/21/2020 |
| 10043 | GeneDX Gaithersburg, MD Lab Technician, Microarray (FT, 40 Hours) BS in medical technology or related Exp: 0-1 year(s) |
Responsibilities include: Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 10044 | GeneDX Gaithersburg, MD DNA Extraction Technician (FT, 40 Hours) BS in medical technology or related Exp: 0-1 year(s) |
Responsibilities include: Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 10045 | GeneDX Gaithersburg, MD DNA Sequencing Lab Technician I BS in medical technology or related Exp: 0-1 year(s) |
Responsibilities include: Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 10046 | GeneDX Gaithersburg, MD NGS Lab Tech BS in medical technology or related Exp: 0-1 year(s) |
Responsibilities include: Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 10047 | GeneDX Gaithersburg, MD Lab Technician, Microarray BS in medical technology or related Exp: 1 year |
Responsibilities include: Implements the standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, takes authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 10048 | Gilead Oceanside, CA Sr. Research Associate I, Process Development (Protein Purification) MS Exp: 0+ years |
Gilead Sciences is seeking a Sr. Research Associate I with experience in protein purification process development to support operations at our biologic’s development and manufacturing site in Oceanside California. Specific Responsibilities and skills for Position: The successful candidate will have a working understanding of downstream process development including centrifugation, normal and tangential flow filtration, chromatography operations, and virus clearance. The ability to demonstrate hands on experience in several of these areas is expected. Experience with multiple modalities (monoclonal antibodies, antibody drug conjugates, virus particles) produced in microbial and mammalian expression systems is a plus. The candidate is expected to work effectively within the purification team to help design and execute experiments supporting process definition, optimization, and characterization with an increasing level of independence. etc. | 9/21/2020 |
| 10049 | Gilead Oceanside, CA Research Associate, Biologics Analytical Operations (Analytical Development) BA/BS in chemistry, biochemistry, or related Exp: 0-2 year(s) |
Job Responsibilities: Under general supervision, performs analytical testing for biologics GMP and process development activities. Follows and incorporates GMP, GDP, and GLP during daily activities within an analytical biochemistry lab setting. Plans and organizes details of experiments for protein analysis. Operates scientific equipment and instruments. Experience and understanding of wet chemistry techniques, chromatography and/or capillary electrophoresis preferred. Uses data, reports, and previous results to identify inappropriate variances and concerns. Participates in group meetings. Presents data or prepares information for others to present. Works with immediate supervisor and teammates on problems of moderate complexity. etc. | 9/21/2020 |
| 10050 | Ginkgo Bioworks Boston, MA QA/QC Engineer BS in chemistry, chemical engineering, or related Exp: 1-6 year(s) |
To realize our dream of building a next-generation organism company, we must ensure that quality is maintained during all stages of our projects, through to the successful deployment of our organisms and processes. Therefore, we’re seeking a QA/QC Engineer with chemical laboratory experience to help define product specification and maintain a Quality Management System. Plus, you’ll ensure that Ginkgo, our customers, and our contract manufacturers have the necessary methods and processes in place, so that we maintain compliance across any required regulatory standard and consistently meet the defined product and process specifications. Responsibilities: Develop, validate, and execute analytical methods, focusing primarily on accurate and precise quantitation. Perform QA/QC data collection, data integration, and data archiving, with the use of Ginkgo’s proprietary LIMS (laboratory information management system). etc. | 9/21/2020 |
| 10051 | Ginkgo Bioworks Boston, MA Downstream Process Engineer BS in chemical engineering, biotechnology, or related Exp: 1-6 year(s) |
To realize our dream of building a next-generation organism company, each of our organisms needs to be successfully deployed. Ensuring that the deployed product reproducibly meets customer and market specification in an economically viable process is critical to Ginkgo’s success. Therefore, we’re seeking a Downstream Process Engineer to help tackle this ambitious challenge. With your passion for process development, and a particular interest in downstream product recovery and purification, you’ll be responsible for designing, developing, and deploying product recovery and purification processes for a variety of products across several scales and sites. Responsibilities: Design and execute laboratory and pilot scale experiments, leading to the definition of commercially viable processes that leverage Ginkgo's engineered organisms. Perform bench scale assays and proof-of-concept experiments. etc. | 9/21/2020 |
| 10052 | Ginkgo Bioworks Boston, MA Medical Technologist (Night Shift) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
We’re seeking highly motivated Medical Technologists to perform routine testing in our high-complexity CLIA laboratory. With a strong focus on quality, accuracy, and efficiency, you’ll be responsible for accessioning received samples, and completing quality control, calibration, maintenance, and proficiency testing in accordance with current laboratory procedures. As a member of Ginkgo’s Clinical Laboratory Operations Team, our Medical Technologists will have a key role in ensuring the success of this important initiative. Please note: this is a fixed-term contractor role for the night shift in our rotation. Anticipated hours are 8:00pm - 8:00am on a "4 days on / 4 days off" shift schedule (which will require some weekend hours). etc. | 9/21/2020 |
| 10053 | Ginkgo Bioworks Boston, MA Medical Technologist (Day Shift) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
We’re seeking highly motivated Medical Technologists to perform routine testing in our high-complexity CLIA laboratory. With a strong focus on quality, accuracy, and efficiency, you’ll be responsible for accessioning received samples, and completing quality control, calibration, maintenance, and proficiency testing in accordance with current laboratory procedures. As a member of Ginkgo’s Clinical Laboratory Operations Team, our Medical Technologists will have a key role in ensuring the success of this important initiative. Please note: this is a fixed-term contractor role for the day shift in our rotation. Anticipated hours are 8:00am - 8:00pm on a "4 days on / 4 days off" shift schedule (which will require some weekend hours). etc. | 9/21/2020 |
| 10054 | Global Pharma Tek Edison, NJ Clinical Project Assistant BS/BA in pharmacy, pharmaceutical science, healthcare informatics or related Exp: 1-2 year(s) |
Job Duties: Responsible for strategic and operational activities of clinical research studies in blood cancer metabolism to ensure adherence to intended timelines and achievements of study goals, while ensuring quality by FDA, EMEA, ICH and GCP guidelines. Facilitating interdisciplinary activities, participating in the clinical trial working group (CTWG), Site Management Team (SMT), and internal team meetings to meet the goals and established timelines. Providing oversight in clinical research Organization (CRO), Central labs and other external vendors to ensure deliverables are met and methods of communication are developed to facilitate an efficient workflow. Providing oversight of activities related to safety reporting compliance. Provide study tracking support (CTMS tracking, start-up tracking, milestone tracking, close-out tracking) and study updates, as requested. Provide coordination and tracking of clinical supply shipments, equipment, and study-specific laboratory samples. etc. | 9/21/2020 |
| 10055 | Global Pharma Tek Edison, NJ Sr. Validation Engineer BS in biochemistry, chemistry, pharmaceutical sciences, or related Exp: 1-2 year(s) |
Job Duties: Writing of Validation documents per Food and Drug Administration (FDA)/Company Guidelines. Utilizing the information from User Manuals, Equipment Operation/Use/Maintenance etc. information and drafting of specification documents and validation protocols for GMP Liquid Dose Manufacturing (LDM) clinical Drug Product (DP) that impact manufacturing facility (processes, equipment (like autoclave, lyophilizers, depyrogenation tunnels). Creation/modification of change control requests, project validation plans and maintaining project within timelines. If any changes were deemed necessary in the equipment (Changes may be like changes in parts or operation of the equipment or changes in procedure or changes in Training of personnel or On-boarding/retiring equipment etc.) I will create a change request in global Quality Tracking System (gQTS), a Trackwise application and thereby monitoring these changes by performing required assignments throughout the project to completion (closing change request) for the current filling and sterilization equipment and install/qualify the new equipment. etc. | 9/21/2020 |
| 10056 | Global Pharma Tek Edison, NJ Submission Specialist – Regulatory Affairs BS/BA in regulatory affairs, healthcare administration, or related Exp: 1-2 year(s) |
Job Duties: Providing direct support to submission project teams, internal RA stakeholders and all functional disciplines responsible for developing and delivering components for submissions. Performing hands-on daily submission compilation and publishing activities associated with preparation of various dossier types and safety reports, for both new product marketing applications and/or marketed product maintenance packages. Performing overall quality of the assigned documents and dossiers which must comply with all internal Bayer best practices, meet global regulatory requirements, and facilitate the review and timely approval by appropriate regulatory authorities. Reviewing the eCTD compliance of dossier-relevant R&D documents/reports from technical perspective. Supporting the compilation of global dossiers and to deliver technically compliant submission documents/reports, which contribute to the development of submissions that meet the technical requirements and standards set by relevant health authorities. etc. | 9/21/2020 |
| 10057 | Global Pharma Tek Edison, NJ Regulatory Affairs Compliance Specialist BS/BA in pharmaceutical science, regulatory affairs, or related Exp: 1-2 year(s) |
Job Duties: The Regulatory Affairs (RA) Compliance Specialist will be responsible for RA Labeling compliance associated with labeling artwork development and revisions for products which may include Rx, OTC/Nutritionals, Cosmetics, and Devices. Specialist will verify the changes in accordance to regulatory requirements to identify impact to product labels. As a key team member, contributes to the labeling processes and procedures to enhance existing practices. Provide Regulatory compliance support in the development, revision, review, and approval of labeling content for regulatory submission, as well as any post marketing labeling changes. Review new and revised labeling for accuracy and for appropriate regulatory requirements. etc. | 9/21/2020 |
| 10058 | Global Pharma Tek Edison, NJ Equipment Validation Engineer BS in mechanical or industrial engineering or related Exp: 1-2 year(s) |
Job Duties: Provide technical support in developing, authoring, and executing the Commissioning, Installation and Qualification protocols for the chromatography skids and other supporting equipment that are used in the production of drug. Develop, Implement and Install filter integrity testing methods to available automated Filter Integrity Testers (FITs) available on site to verify the integral of the vent filters that will used in the process for WFI Tanks, Autoclaves, supply clean compressed air and as required. Prepare protocols and reports for Validation Project Plan, Validation Master Plan, IQ, OQ, OQ, Traceability Matrix, Engineering test Plans, and Commissioning test strategies following the site Good Data and Documentation Practices (GDP) during protocol execution for qualifying the system or facility. etc. | 9/21/2020 |
| 10059 | Global Pharma Tek Edison, NJ Laboratory Equipment/Instrument Qualification Engineer BS in pharmacy, chemistry, or related Exp: 1-2 year(s) |
Job duties: Execute Validation and Qualification protocols which include installing, operating and maintaining of GMP Lab Equipment and Instruments (HPLC, UV-Vis Spectrometers, FTIR, GC, pH meters, Conductivity meters, Analyzers etc.) and manufacturing equipment like sterilizers and autoclaves to confirm if the instrument is compatible and compliant with Manufacturing, analysis, Company and FDA regulations. Author, review and approve validation and qualification documents for Lab Equipment/Instruments and manufacturing equipment in compliance with Pharma and FDA guidelines through Document Management system tool. Perform validation and qualification documents include User requirement specifications, functional requirement specifications, Installation Qualifications (IQ), Operational Qualifications (OQ), Performance Qualifications (PQ), Validation summary reports, Change Control etc. for various lab instruments utilized by Quality control and Quality assurance teams. etc. | 9/21/2020 |
| 10060 | Global Pharma Tek Edison, NJ Associate Operations Specialist BS in pharmacy, pharmacology, or related Exp: 1-2 year(s) |
Job duties: Review, assess and process Lifecycle Safety data and information, across all service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Receive, triage, review and process data from various sources on time, within budget and meet quality standards. Perform data entry for tracking and safety database, coding relevant medical terminology, writing, descript narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations and ensuring reports are sent to the customer within assigned deadlines. etc. | 9/21/2020 |
| 10061 | GRAIL Menlo Park, CA Laboratory Technician I/II BS in a relevant scientific field Exp: 1-5 year(s) |
GRAIL is seeking a Laboratory Technician I/II for the R&D Laboratory Management team, who will be primarily responsible for ensuring the efficient operation of GRAIL Research and Development activities. The ideal candidate is a detail-oriented, dynamic team player with experience in both automated and manual molecular biology workflows combined with strong interest in NGS methodologies. The candidate will be expected to partner with many functions of our organization - Automation, Product Development, LIMS, Supply Chain, Biosample Operations, and Clinical Lab - to ensure the successful completion of R&D projects and general Operational support. etc. | 9/21/2020 |
| 10062 | GRAIL Menlo Park, CA Equipment Engineering Technician BS in an engineering or scientific discipline Exp: 0-2 years |
As an Equipment Engineering Technician, you are responsible for supporting laboratory equipment management procedures, in alignment to our internal Quality Management System, to ensure superior performance within Laboratory Operations. This will include global laboratory equipment support, sustainment, and operations activities across Production/Clinical, Product Development, Research and Development laboratories, in accordance with CLIA, cGMP and/or GLP guidelines. You Will: Support global laboratory equipment documentation by maintaining internal equipment records into our database/repository. Assist with internal laboratory equipment inventory processes and procedures. etc. | 9/21/2020 |
| 10063 | Grand River Aseptic Manufacturing Grand Rapids, MI Validation Engineer I BS in engineering or related Exp: 0-3 years |
Support validation of cGMP equipment, facilities and processes. These duties will include, but are not limited to: and validation of laboratory systems, production equipment, manufacturing processes and utilities. ESSENTIAL DUTIES & RESPONSIBILITIES: Assist with maintaining and revising validation procedures. Establish and maintain good practices with regards to processes and/or internal conditions leading to an aseptic environment. Establish and execute programs covering equipment, processes, cleaning, process and computer system validation. Assure that all validation is performed to conform to GRAM’s and cGMP requirements. Provide validation support to internal customers such as Technical Services, Quality Control, Manufacturing and other users of validation services. etc. | 9/21/2020 |
| 10064 | Gritstone Oncology Cambridge, MA Research Associate - GMP NGS BS Exp: 1+ year(s) |
The primary role of the Research Associate is to be responsible for the execution of established histology, and next-generation sequencing assays in the GMP Next Generation Sequencing (NGS) laboratory. This team is responsible for the GMP compliant processing of cancer patient samples through nucleic acid extraction and next generation sequencing. The ideal candidate will have patient-centric approach and experience in a regulated environment (CLIA/CAP, cGMP) and will be expected to maintain batch record reports, consumable inventory, equipment maintenance and calibration to maintain quality control and compliance. Individuals with experience as a Clinical Lab Technologist or Molecular Technologist are encouraged to apply. etc. | 9/21/2020 |
| 10065 | Harpoon Therapeutics South San Francisco, CA Research Associate, Protein Purification BS/MS in biochemistry, biotechnology, molecular biology, or related Exp: 1-5 year(s) |
We are seeking a highly motivated individual who enjoys detail-oriented technical work, can manage diverse responsibilities in the lab, and thrives in a fast-paced work environment. As an integral member of our functional group, this individual will work closely with other team members within Protein Science and partner with other functional areas including Biology, New Technologies, and Translational Medicine. The ideal candidate will have strong technical aptitude for lab work and a problem-solving mindset that is diligent and flexible. Our Research organization is comprised of a small but diverse group of scientists with a wide range of experience and backgrounds. etc. | 9/21/2020 |
| 10066 | Harpoon Therapeutics South San Francisco, CA Research Associate, Biology BS/MS in cell biology, biochemistry, or related Exp: 1+ year(s) |
The Research Biology group at Harpoon Therapeutics seeks a Research Associate to join our team. Responsibilities include testing of samples in support of both preclinical development and clinical programs, assay development and optimization, and collection of data in support of regulatory filings. Applicants should be capable of working flexibly and expeditiously in a collaborative, innovative and inspiring environment. The ideal candidate will have experience with mammalian cell culture, stable cell line generation, luciferase assays, flow cytometry, and bioassay automation. Good communication skills, good planning, and an ability to meet deadlines are essential. etc. | 9/21/2020 |
| 10067 | Helix San Diego, CA Research Assistant, Research & Development BS/MS in a biological science or related Exp: 1 year |
We are searching for a highly motivated and team-oriented Research Assistant (RA) to support a wide variety of molecular biology, biochemical, and extraction techniques to support projects focused on viral infection. As an RA at Helix, you will work in a dynamic and fast-paced environment to perform robust, scalable COVID-19 testing, where you will perform testing with the overall goal of providing results that will be used for the assay development, diagnosis and management of COVID-19. As a Research Assistant, Research & Development you will: Assist in running molecular assays and processes for Next Generation Sequencing (NGS) for use in a high throughput clinical laboratory. Perform routine tasks for the group. Execute experiments related to NGS assay. etc. | 9/21/2020 |
| 10068 | Helmer Scientific Noblesville, IN Assembler Level II HS diploma or equivalent Exp: 1-3 year(s) |
The Assembler II performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. Cross-trained to perform specialty functions in the following areas: brazing, final testing, charging or wiring. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. etc. | 9/21/2020 |
| 10069 | Helmer Scientific Noblesville, IN General Fabricator 2nd Shift HS diploma or equivalent Exp: 1-3 year(s) |
The General Fabricator: Operates painting and other operations in the fabrication department. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. etc. | 9/21/2020 |
| 10070 | Helmer Scientific Noblesville, IN Fabrication Technician HS diploma or equivalent Exp: 1-3 year(s) |
The Fabrication Technician: Operates and maintains the laser, Turret Punch, CNC press brakes or panel bender. Will be cross-trained to perform responsibilities on any of these machines. etc. | 9/21/2020 |
| 10071 | Helmer Scientific Noblesville, IN Assembler Level I 2nd Shift HS diploma or equivalent Exp: 1-3 year(s) |
The Assembler I: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. etc. | 9/21/2020 |
| 10072 | Helmer Scientific Noblesville, IN Assembler I - Clean & Pack HS diploma or equivalent Exp: 1-3 year(s) |
The Assembler I - Clean & Pack: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. etc. | 9/21/2020 |
| 10073 | Helmer Scientific Noblesville, IN Assembler Level I HS diploma or equivalent Exp: 1-3 year(s) |
The Assembler I: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. etc. | 9/21/2020 |
| 10074 | Helmer Scientific Noblesville, IN Sustaining Mechanical Product Support Engineer 1 BS in mechanical or related engineering Exp: 0-3 years |
The Sustaining Mechanical Product Support Engineer 1: Provides product support to Manufacturing and Sustaining Engineering departments through the development, documentation and production support for Helmer product portfolio. Support projects, specification updates and engineering requirements based on product and stakeholder requirements. Enhance part and product design, quality, manufacturability, and serviceability through sustainment and continued improvement of mechanical designs including assembly/component design and testing, tolerance stack, non-conforming product evaluation and value engineering. etc. | 9/21/2020 |
| 10075 | Exelixis Alameda, CA Temporary Purchasing Assistant AA/BA Exp: Not necessary for AA/BA candidates |
Responsible for supporting the daily tasks, functions, and responsibilities of the Procurement Department and the Indirect Buyers which will focus on, but is not limited to, entering Vendor Master data into SAP for new vendors and vendor changes including following security procedures to confirm and document change requests, placing routine orders as assigned, and, follow-up on orders. Additional projects as assigned by manager. Position Requirements: ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsible for supporting the day-to-day purchasing for the company by: Managing vendor data entry and vendor changes in the ERP system. Expediting and PO follow-up. Filing and clerical support duties. etc. | 9/14/2020 |
| 10076 | Exelixis Alameda, CA Assistant Research Scientist I (Pharmacokinetics/Pharmacodynamics) BA/BS Exp: 0-2 years |
The successful and highly motivated candidate will support the in vivo pharmacology research program and contribute to the multidisciplinary research team by designing and executing in vivo studies to determine pharmacokinetics and pharmacodynamics relationships and efficacy of optimized leads. Position Requirements: ESSENTIAL DUTIES AND RESPONSIBILITIES: Conduct in vivo studies in mouse and/or rat models to assess pharmacological characteristics of preclinical drug candidates. Daily dosing (po, iv, ip) of preclinical drug candidates to mice or rats, followed by blood and tissue collection for pharmacokinetic or pharmacodynamic analyses. Tumor implantation and measurement for long-term efficacy and pharmacodynamic studies. Use of aseptic techniques to grow and scale up tumor cells for implantation in mouse models. etc. | 9/14/2020 |
| 10077 | Exonbio San Diego, CA Research Associate MS in biology Exp: 1 year |
We are looking for a RESEARCH ASSOCIATE to join our antibody development team. Requirements: One year experience in Cell culture and banking, PCR, Protein purification with AKTA. | 9/14/2020 |
| 10078 | Bio-Techne San Marcos, CA Packaging Technician HS diploma or equivalent Exp: 1-2 year(s) |
As a packaging technician you will perform filling, kitting, and labeling functions. Key Responsibilities: Assist in the setup and running of automated liquid filling, labeling and packaging equipment. Assist in the setup and running of manual liquid and powder portable filling equipment. Perform daily filling, labeling, kitting duties according to the production schedule. Comply with Good Manufacturing Practices (GMP’s) and Quality Systems Regulations (QSR). General organization of filling, labeling and packaging tasks. Inspect all materials being issued to and returning from shop orders. Accurately count and return all materials. Maintain supplies for the CER, and packaging areas. etc. | 9/14/2020 |
| 10079 | Bio-Techne Minneapolis, MN Research Associate BS/BA Exp: 0-3 years |
This position is responsible for filtering, aliquoting, and storing finished proteins products using aseptic techniques in a GMP Lab, following GMP guidelines. Run lyophilizer and perform fill finish (vialing, stoppering, crimping, and labeling of products). Documents batch records following GMP guidelines. Manufacture and bag ProDots. Buffer manufacture for fill finish. (80%) Documentation: SOPs, and for validation/maintenance/cleaning of equipment and facilities. (20%) Key Responsibilities: Filter, aliquot, and bottling of product using aseptic techniques. Run lyophilizer and perform fill finish (vialing, stoppering, crimping, and labeling of products). Manufacture and bag ProDots. etc. | 9/14/2020 |
| 10080 | Bio-Techne Devens, MA Advanced Quality Technician BS Exp: 1+ year(s) |
Advanced Quality Technician reports to the Quality Control Manager and is responsible for in-process and final QC testing of Bionostics products. In addition, Advanced Quality Technician participates in instrument validations, performs lab maintenance activities, initiates collaborations, monitors laboratory and process inventories, conducts device history record review, and creates certificates of analysis for commercial products. Key Responsibilities: Understands and adheres to all quality technician job requirements. Follows work instructions carefully and demonstrates good documentation practices. Documents results, processes testing, and refers to past batch records when needed. etc. | 9/14/2020 |
| 10081 | Bio-Techne Wallingford, CT QC Technician AS/AA Exp: 0-3 years |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including hands-on evaluation of microfluidic cartridge products. Key Responsibilities: Understand and follow appropriate quality protocols: Quality Manual; Record Keeping Guidelines; General understanding of Quality body of knowledge (Inspection plans, sampling, etc.); Safety procedures; Department specific SOP’s. etc. | 9/14/2020 |
| 10082 | Bio-Techne San Jose, CA Manufacturing Technician (Kitting) Unspecified Exp: 0-1 year |
The technician will work as part of the kitting team under the planning group to complete all tasks related to subassemblies and top-level product kits, packaging and labeling to prepare products for warehousing and/or shipments to customers. Key Responsibilities: Follow SOPs, work instructions and/or drawings to ensure product specifications are met. Assemble, label, and package a wide variety of kits: product components, sub kits and top-level kits. Prepare a collection of product components, sub kits and top-level kits for shipping (Pick to Order, PTO). Prepare demo kits as needed. Stage material for kitting operation. Inspect collection of kit components for expiration dates. Submit daily kitting numbers and associated types (sub kits / top-level kits) to manager at end of shift. etc. | 9/14/2020 |
| 10083 | Bio-Techne Minneapolis, MN Advanced Research Associate MS in biology, cell biology, immunology, or related scientific discipline Exp: 0-2 years |
The responsibilities of this position are to develop bioassays on proteins and antibodies to ensure quality products. Maintain cell lines and isolate primary cells for use in the assays. Key Responsibilities: Develop cell-based and functional ELISA binding bioassays for new protein products and improve existing bioassays. Review literature and discuss the new products and experiments with the supervisor. Implement new bioassays under the direction of the supervisor. Write SOPs for new developed bioassays and perform stability testing on new products. Perform product bioassays following the SOPs and assist at all stages of protein expression and purification. Maintain cell lines and isolate primary cells from human or animal blood or tissues for use in bioassays. Freeze stock of cells for future use. etc. | 9/14/2020 |
| 10084 | Bio-Techne San Marcos, CA Chemist I - R&D (Temporary) BS/BA Exp: 0-3 years |
This position is responsible for the developing and or formulation of controls, calibrators, working solutions, and intermediates in the production and development of Bio-Techne's various product lines. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. Key Responsibilities: Assist with preparation and/or development of new products using approved procedures and keep detailed and accurate records. Set up and conduct experiments that help further new product development. Follow standard operating procedures. Perform in process analysis and determine adjustments to bring analytes into specification. etc. | 9/14/2020 |
| 10085 | Exsurco Wakeman, OH Assembly Technician HS diploma Exp: 3 months |
Primary role is to perform all forms assembly activities including equipment setup and tear down where required as well as in-process verifications. In addition, this position includes several cross-functional responsibilities comprising Shipping, Receiving, Job Picking, Warehousing and Plant Cleaning and some Maintenance activities. This position also has responsibilities associated with Servicing returned products (disassembly and reassembly, diagnosis and report writing). RESPONSIBILITIES: The duties & responsibilities of the Assembly Technician include, but are not necessarily limited to the following: Perform bench-type processes to complete mechanical and electrical assemblies and sub-assemblies, using hand tools, and electronic and pneumatic tooling. Assemble Exsurco product and equipment as required. etc. | 9/14/2020 |
| 10086 | Fate Therapeutics San Diego, CA Research Associate III / II, Genomics Unspecified Exp: 1-3 year(s) |
Fate Therapeutics is currently seeking a talented and highly motivated Research Associate with a background in nucleic acid purification and next generation sequencing (NGS) library processing to join a multidisciplinary team dedicated to the discovery and characterization of novel induced pluripotent stem cell (iPSC)-derived cellular therapeutics. The candidate will play a key role in Fate’s Genomics group, executing-based assays in support of Fate’s efforts to generate and characterize best-in-class iPSC-derived cellular therapies. The ideal candidate will be highly collaborative and communicative and have extensive hands-on experience in extracting and purifying DNA and RNA from cells and tissues for use in NGS. This position will require adherence to tight deadlines, strong independent and collaborative research abilities, a high level of organization, and the ability to communicate effectively across multidisciplinary teams. etc. | 9/14/2020 |
| 10087 | Fate Therapeutics San Diego, CA Clinical Manufacturing Associate BS/BA in a biological science Exp: 1-2 year(s) |
Fate is currently seeking a motivated associate to join our Clinical Manufacturing team. The successful candidate will execute CMC studies and produce cell stocks in support of Fate's clinical development programs. The position will be responsible for ordering and maintaining lab equipment and supplies, performing experiments to qualify process improvements for manufacture of Fate's products in clinical development, and performing analysis of data. The position will provide technical support for Fate manufacturing and process development activities. The successful candidate will have excellent organizational and communication skills, a keen attention to detail and thrive in a team environment. etc. | 9/14/2020 |
| 10088 | FHC Bowdoin, ME Shipping & Receiving Technician AS/BS Exp: Not necessary for AS/BS candidates |
The Shipping & Receiving Technician is responsible for all of FHC, Inc.’s incoming and outgoing shipments. The position requires a basic knowledge of FHC products and an extensive knowledge of shipping requirements. Interfacing with multiple departments to ensure the best delivery dates and methods are used to meet customers’ requirements and to assure a unique and satisfying experience for both internal and external customers. ESSENTIAL DUTIES AND RESPONSIBILITIES: Other duties may be assigned. Responsible for processing Return Material Authorizations RMAs Inbound and Outbound. etc. | 9/14/2020 |
| 10089 | Finch Somerville, MA Process Development Associate BS in chemical or biomedical engineering, chemistry, or biochemistry Exp: 0-2 years |
Duties / Responsibilities: Assist in planning, executing, and documenting studies related to design of novel drug products. Support scale-up and technical transfer of production processes to GMP Manufacturing. Assist with troubleshooting, root cause analysis, and identification of corrective actions to support Pharmaceutical Development or GMP Manufacturing equipment and process issues. Work cross-functionally across Quality, Research, Clinical, and Manufacturing teams to achieve company goals. Source and maintain relationships with vendors and Contract Manufacturing Organizations. etc. | 9/14/2020 |
| 10090 | Foundation Medicine Cambridge, MA Molecular Technologist I BS in a science Exp: 1+ year(s) |
The Molecular Technologist I performs procedures in a complex patient sample testing process with limited supervision. Most prominently, the position is responsible for solution and reagent preparation, equipment maintenance, and the handling and testing of patient specimens. The incumbent works one of three established shifts and may be assigned to work any day that the lab is operational. Key Responsibilities: Prepare the Next Generation Sequencing (NGS) library. Under limited supervision of senior lab personnel and in adherence to established Standard Operating Procedures (SOPs): Extract and isolate nucleic acids. Complete hybridization capture, and genetic sequencing methods. Operate automated 8-span and 96-head liquid handling platforms. etc. | 9/14/2020 |
| 10091 | Foundation Medicine Cambridge, MA Histotechnician (Contract) AS/AA Exp: 1+ year(s) |
The Histotechnician performs routine testing in FMI’s high complexity clinical diagnostic laboratory and is responsible for receipt of patient samples as well as the preparation of samples for microscopic examination and analysis by Pathology. This role focuses on cutting, mounting, staining, and batching slides. Key Responsibilities: Operate a microtome to produce slides or curls from paraffin blocks. Prepare and initiate samples for nucleic acid extraction. Manage sample movement through lab facilities. Ensure and maintain molecular safe integrity and quality of the specimens. etc. | 9/14/2020 |
| 10092 | Foundation Medicine Cambridge, MA Bioinformatics Scientist I MS in biochemistry, bioinformatics, computer science, or related Exp: 1+ year(s) |
The Scientist I, Bioinformatics develops novel methods for detecting, reporting and analyzing alterations in tumor DNA and RNA, while optimizing existing methods. The incumbent provides scientific and technical contributions for a designated project on an interdisciplinary team. The Scientist I, Bioinformatics is also responsible for supporting novel biomarker and companion diagnostics development by mining and analyzing various types of data generated during the product development and validation process. etc. | 9/14/2020 |
| 10093 | Foundation Medicine Morrisville, NC Accessioning Technician II BS/BA Exp: 0-1+ year(s) |
The Accessioning Technician II performs critical sample receipt and data entry functions in FMI’s CLIA-certified clinical laboratory. Specifically, the Accessioning Technician II receives incoming samples and ensures that necessary information has been received to move forward with processing. The Accessioning Technician II is assigned to one of three shifts and may be assigned to work any day that the lab is operational. This is a regulated position and additional information may be available from FMI Quality Assurance regarding regulatory guidelines. etc. | 9/14/2020 |
| 10094 | Fresenius Kabi Melrose Park, IL Associate Chemist (1st Shift) BS in chemistry Exp: 0-3 years |
Responsible for the chemical analysis of raw material, in-process, stability and finished products as required for QC. Effectively communicates work and results both orally and in writing. PRINCIPAL ACTIVITIES PERFORMED BY THE INCUMBENT: Performs accurate routine chemical testing, such as wet analysis, assays, water testing and physical testing in full compliance with company directed SOP’s. Reviews SOP’s for applicability and notifies supervisor for necessary changes when needed. Maintains accurate records of all work performed with respect to a given project. Meets facility audit as well as cGMP or GLP requirements. etc. | 9/14/2020 |
| 10095 | Fresenius Kabi Melrose Park, IL Validation Engineer BS/BA in science or engineering Exp: 1-3 year(s) |
We currently have an opportunity for a Validation Engineer in our Melrose Park Pharmaceutical Manufacturing facility who will provide technical support to operations with equipment/system/process initial validation and equipment/system/process requalifications. This is a first shift position. Weekends and off-shift hours are periodically required. Responsibilities: Schedules and executes equipment requalifications per Standard Operating Procedures (SOPs). Coordinates and communicates all testing with affected functional groups and evaluates test results. Assembles and composes the final report and circulates for approval. Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to include protocol preparation, scheduling, protocol execution, and final report preparation. etc. | 9/14/2020 |
| 10096 | Fresenius Kabi Wilson, NC Project Engineer BS in engineering Exp: 1-3 year(s) |
This position is responsible for procurement, design and integration of equipment, process systems and corresponding utilities. Leads the project from initial design studies to final validation, and maintains project schedule and budget while communicating results to all stakeholders. PRINCIPAL ACTIVITIES PERFORMED BY THE INCUMBENT: Conducts accurate Engineering Studies to develop design space, used for manufacturing construction, process development, equipment procurement and validation master plan. Develops and manages site projects by employing past experience, research, design and concept sketches, layouts, drawings, vendor interaction, preparation of specifications, discussions with appropriate management and site personnel. etc. | 9/14/2020 |
| 10097 | Fresenius Kabi Melrose Park, IL Associate Scientist (Night Shift) BS in a biological science Exp: 1-2 year(s) |
Responsible for performing routine testing of in-process and finished product samples. Monitors environmental conditions in the production and lab areas. Summarizes environmental monitoring and product test results. Provides project support to Scientist and Lead Scientist. Prepares media and reagents and equipment. Responsibilities: Generates new standard operating procedures for microbiology test procedures. Keeps others current as assigned. Performs environmental monitoring for Skan isolators and routine testing of in-process and finished products. Assists Scientist / Lead Scientist with test method validations and special projects. Carries out special projects independently as required and assigned by supervision. Assists with plant equipment requalifications as directed. etc. | 9/14/2020 |
| 10098 | Fresenius Kabi Melrose Park, IL Aseptic Filling Operator I (Day Shift) HS diploma or equivalent Exp: 1-2 year(s) |
Responsible for setting up, operating and monitoring fill equipment per Standard Operating Procedures and current Good Manufacturing Practices. Must be knowledgeable of and practice good aseptic technique to minimize potential for product contamination. Principal Activities Performed By The Incumbent: Practices aseptic technique at all times while working in aseptic areas. Complies with current SOP’s and cGMPs. Maintains aseptic gowning requirements. etc. | 9/14/2020 |
| 10099 | Fresenius Kabi Melrose Park, IL Quality Inspector I (Day Shift) HS diploma or equivalent Exp: 1-3 year(s) |
Responsible for visually inspecting filled product off the filling line following Standard Operating Procedures (SOP) and current Good Manufacturing Processes (cGMP). The production inspector will work in the Capping Department and on the off-line inspection area and therefore must be knowledgeable of procedures and equipment in each area. Responsibilities: Principal Activities Performed By The Incumbent: Visually inspects products for various defects. Documents work accurately and timely. Complies with current SOP’s and cGMP’s. Sets-up, adjusts, and operates equipment such as inspection machines, cappers, etc. | 9/14/2020 |
| 10100 | Fresenius Kabi Melrose Park, IL Quality Inspector I (Night Shift) HS diploma or equivalent Exp: 1-3 year(s) |
Responsible for visually inspecting filled product off the filling line following Standard Operating Procedures (SOP) and current Good Manufacturing Processes (cGMP). The production inspector will work in the Capping Department and on the off-line inspection area and therefore must be knowledgeable of procedures and equipment in each area. Responsibilities: Principal Activities Performed By The Incumbent: Visually inspects products for various defects. Documents work accurately and timely. Complies with current SOP’s and cGMP’s. Sets-up, adjusts, and operates equipment such as inspection machines, cappers, etc. | 9/14/2020 |
| 10101 | Freudenberg Baldwin Park, CA Quality Specialist - Process Monitoring and Material Release BS Exp: Not necessary for BS candidates |
Your tasks: Complete all incoming/raw material and component inspections, to include verifying all documentation, and properly identify/release those materials in ERP. Perform inspection and verification of incoming materials, to include subcomponents and molded parts that have undergone off-site processing such as laser etch coatings, etc. Supports in the review and disposition of raw material, in-process and finished goods to include (NCMR/sNCMR/Material Hold Quality Notifications), departmental training/cross-training, Coordinates and monitors calibration requirements of test, measurement, and diagnostic equipment (TMDE). Administers assignment of new TMDE asset numbers, calibration requirements, calibration frequencies, and their control. Generates and investigates non-conformance reports (OOT’s – Out of Tolerance Reports) when TMDE is found to be out of calibration or missing calibration interval. etc. | 9/14/2020 |
| 10102 | Freudenberg Baldwin Park, CA Maintenance Technician - 1st Shift HS diploma or equivalent Exp: 1-3 year(s) |
Your tasks: Maintaining and repairing the physical structure of the building, grounds, injection molding machines and auxiliary equipment. Painting and performing structural repairs to masonry, woodwork, and furnishings of buildings. General cleaning and up keep of buildings, including buffing, dusting, sweeping, mopping, vacuuming, and washing windows. Assist other departments as requested, including moving furniture, unloading, and storing supplies. Perform preventative and corrective maintenance on assigned equipment. Diagnose and repair electrical, hydraulic, and pneumatic control system problems on production machinery, auxiliary equipment and fixtures. Plan, layout and install electrical, hydraulic, and pneumatic systems in support of the fabrication and installation of new equipment and fixtures. etc. | 9/14/2020 |
| 10103 | Frontage Exton, PA Associate Scientist, Analytical Services-CMC BS in chemistry Exp: 1-2 year(s) |
Responsibilities: Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines. Assists method development Performs method validation under supervision. Reports and resolves any unexpected issues under supervision. Complies with all relevant cGMP and/or GLP regulatory requirements while carrying out assigned studies. etc. | 9/14/2020 |
| 10104 | Frontage Exton, PA Scientist MS in biology, biotechnology, or related Exp: 6 months |
For a contract research organization (Frontage Laboratories, Inc. – Exton, PA): design/develop method transfer, method development, validations, quantitation and structure elucidation; perform high-volume bio-analytical sample analysis; perform data analysis, data quality control (QC) and data interpretation for bio-analytical, PK, PD and ADME studies in regulated environment; utilize and maintain analytical instruments, including Liquid Chromatography Tenderm Mass Spectrometry (LC-MS/MS) and Nuclear Magnetic Resonance (NMR); perform technical work related to the care and use of research animals. etc. | 9/14/2020 |
| 10105 | Frontage Exton, PA Associate Scientist-Product Development- CMC MS in pharmaceutical sciences, polymer chemistry, microbiology, or chemical engineering Exp: 0-4 years |
Responsibilities: Perform assigned tasks per procedures compliant with cGMPs and participate in the clinical manufacturing of parenteral, ophthalmic, and other sterile dosage forms. Participate in media fills for aseptic fill projects. Assist in the equipment set up, operation, maintenance, cleaning as required for the project. Perform Environmental Monitoring (EM) of manufacturing areas per applicable SOPs and maintain records. Assist with manufacturing area maintenance such as area monitoring and qualification, purchase of gowning supplies, purchase of equipment and room cleaning supplies, microbiological monitoring supplies. Maintain records for personnel gowning qualification. etc. | 9/14/2020 |
| 10106 | Frontage Exton, PA Scientist-002 MS in biology, biomedical science, or related Exp: 1 year |
Job Duties: Conduct in vitro and in vivo metabolism studies using radiolabeled and non-radiolabeled compounds. Conduct bioanalytical assays using HPLC and LC/MS/MS. Use LSC and sample oxidizers to generate data for radioactive mass balance studies. Develop sample analysis method and perform metabolites identification. Isolate and identify radioactive and non-radioactive metabolites from in vivo and in vitro. Provide routine animal care and perform technical work related to the care and use of research animals. Maintain mammalian and primary cell lines for preclinical experiments. Perform work in regulated environment. etc. | 9/14/2020 |
| 10107 | Frontage Exton, PA Scientist- Bioanalytical Services-ICP-MS MS in analytical chemistry, biochemistry, pharmacology, or related Exp: 1+ year(s) |
Scientist / Bioanalytical Services Essential Functions Run sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. Candidates with experience in ICP-MS and/or ICP-MS/MS for bioanalytical or other applications are preferred. Duties: Perform high-volume sample analysis and/or data analysis, data QC, and data interpretation. Maintain schedule of projects and timelines. Coordinate study activities with Principle Investigator to ensure efficiency and quality. Aid in the preparation of study summaries and/or reports. etc. | 9/14/2020 |
| 10108 | Frontage Spring House, PA Scientist-STE Assay Development MS in biology, chemistry, biochemistry, or related Exp: 1-2 year(s) |
This laboratory-based position is in the Soluble Target Engagement (sTE) Assay Development group within the Bioanalytical Sciences department. Develop assays to quantify biopharmaceutical drug targets in various sample matrices from non-clinical and clinical studies; Perform and interpret complex in vitro, ex vivo and in vivo experiments with some independence; Analyze and present data in professional format; Demonstrate clear and professional verbal and written communication; Conduct, analysis and reporting of data in accordance with requirements set forth by the department; Ensure maintenance of detailed documentation of assay development and qualification; Record experimental data and accurate and highly organized laboratory notebooks; Follow appropriate SOPs and all internal documentation requirements. etc. | 9/14/2020 |
| 10109 | Frontage Exton, PA Scientist-PK/ADA BS/MS in a biology related field Exp: 1-2 year(s) |
Performs biologics method transfer, method development and validation according to FDA guidance, Frontage SOP and industry practices. Performs sample analysis following SOPs and methods, prepare, review the data package and reports. Provide training and technical guidance to the junior scientists. Provide assistance to project management to ensure meeting the requirements of project quality, and timelines. Provide assistance to the PI/RS to ensure the compliance. etc. | 9/14/2020 |
| 10110 | Fujifilm Diosynth College Station, TX Manufacturing Technician I/II AS in biology, microbiology, chemistry, engineering, or related Exp: 0-1+ year(s) |
Essential Functions Include: Write and review standard operating procedures, buffer formulation records and batch production records. Assist senior staff in implementing project safety and quality assurance programs in accordance with SOPs. Maintain the confidentiality of proprietary company information. Document and maintain activity records according to cGMP regulations and ensure junior team members are trained. Operate general production equipment such as Autoclaves, Glass washers, Incubators, Analytical Scales, pH/conductivity meters, etc. Perform daily cleaning and sanitization of the laboratory and manufacturing areas. Maintain an effective working relationship with others. etc. | 9/14/2020 |
| 10111 | Fujifilm Diosynth College Station, TX Manufacturing – Associate Process Engineer BS in science, engineering, or related Exp: 1 year |
Develop and maintain equipment and unit operation standards and procedures utilizing 4M (Man, Materials, Machinery and Methods) approach including: Support new equipment purchasing, URS creation and or revision, equipment qualification and procedure creation and or revision. Creation and or revision of recipe or methods for various platforms. Review and/or Approve equipment qualification limits. Review Calibration Tolerances and Approve Out of Tolerance Investigations. Develop and approve procedures for new equipment being introduced into the plant. Support new product transfer by creation or revision of the Process Consumable List. etc. | 9/14/2020 |
| 10112 | Fujifilm Diosynth College Station, TX Maintenance Technician I – Night Shift AS/AA in engineering, maintenance, bioengineering, or related Exp: 1 year |
Essential Functions: Provide maintenance and operational support for clean utility equipment such as clean gases, steam generated Water for Injection (USP), clean steam systems, and RODI water systems. Provide maintenance and operational support for plant utility equipment, including utilities such as air compressors, air dryers, steam boilers, chillers, heating hot water boilers, HVAC systems and waste disposal systems. Provide maintenance and operational support for facilities, building maintenance and grounds. Technician will assist senior technician on critical environment controls, maintenance on critical laboratory equipment within GMP clean rooms and environmental controlled areas. Able to work with operators and technicians in helping to perform troubleshooting tasks on temperature controlled process equipment, such as bioreactors, centrifuges, micro-filtration skids, and autoclaves. etc. | 9/14/2020 |
| 10113 | Fujifilm Diosynth College Station, TX Facilities Engineer I BS in electrical, chemical, mechanical, or biomedical engineering Exp: 1 year |
Essential Functions: Responsible for providing engineering, operational and troubleshooting support to facilities, utilities and process equipment as needed. Responsible for monitoring complex equipment and maintaining the equipment with a minimum of downtime. Responsible for developing, writing, editing and/or reviewing SOPs, JHAs, HECPs, P&IDs and operations/maintenance procedures for facilities, utilities and process equipment. Responsible for the implementation of process improvements and corrective actions as well as the development of maintenance strategies and equipment life cycle. Responsible to support equipment IQ/OQ/PQ or any other validation startup activity as required. Responsible to support Reliability Centered Maintenance (RCM) activities including condition monitoring and predictive technologies as applicable. etc. | 9/14/2020 |
| 10114 | Fujifilm Diosynth College Station, TX Drug Product Operations – Technician III MS in biology, microbiology, chemistry, engineering, or related Exp: 1 year |
Essential Functions: Responsible for the operation of Vanrx SA25 Vial Filling Isolator. Responsible for assisting in the formulation of the bulk drug product in accordance to procedures. Responsible for visual inspection and labeling of filled bulk drug product vials in accordance to procedures. Assist in writing, reviewing, and/or updating Standard Operating Procedures (SOPs) and Batch Production Records (BPRs). Document and maintain activity records according to cGMP regulations and ensure junior team members are trained. Help implement project safety and quality assurance programs in collaboration with senior staff and EH&S. etc. | 9/14/2020 |
| 10115 | Immunomic Therapeutics Rockville, MD Process Development Associate I-II MS in sciences Exp: 0-1 years |
Reporting to the Sr. Manager, Process Development, this position will be responsible for the upstream processes used in nucleic acid vaccine production including bacterial transformation and fermentation. Incumbent will become proficient in other areas including plasmid purification, transient transfection, and Western blotting in support of the Process Development (PD) laboratory at ITI. | 8/29/2020 |
| 10116 | Immy Norman, OK Quality Assurance Technician I Associates in science or engineering Exp: 0-2 years |
Under moderate supervision, the Quality Assurance Technician I is responsible for performing all monthly, quarterly, and yearly calibrations of laboratory equipment, maintaining equipment lists, performing quality inspections on incoming items, and manufacturing materials needed to support the Quality Management System. | 8/29/2020 |
| 10117 | Immy Norman, OK Medical Records Technician Associates in sciences or Med Lab technician certification Exp: 1-2 years in lab |
The purpose of this position is to support IMMYLabs in clerical duties in a manner that is consistent with medical, administrative, legal, and regulatory requirements. This position will process, maintain, compile, and report information in a standard manner consistent with all reporting agreements. | 8/29/2020 |
| 10118 | Immy Norman, OK Upstream Technician BS/BA in biological sciences Exp: 0-2 years in lab |
The Upstream Technician is responsible for the manufacture of immunoassays. This includes buffer manufacturing, testing, and manipulation for all products lines (LFA, EIA, Complement Fixation, Latex Agglutination, and Immunodiffusion). This person will perform various types of conjugations, quantifications, purifications, and antigen/antibody pairing and must have a high attention to detail. Upstream Technicians will be trained to excel in one product line before training in another. | 8/29/2020 |
| 10119 | Immy Norman, OK Systems Analyst Degree or pursuing a degree in IT related field Exp: 0-1 years |
The systems analyst helps support, validate, maintain, and test software and other technology systems. This position participates in design and testing activities with other staff members. | 8/29/2020 |
| 10120 | Immy Norman, OK PCR Specimen Processing Technician HS Diploma/GED, AA or BS/BA, or MT/MLT certification Exp: 1-2 years in lab |
The primary responsibility of this position is to handle incoming samples for accessioning, organizing, storing, and processing. Processing of samples will include DNA isolation of various sample types, prep for PCR and running PCR testing. | 8/29/2020 |
| 10121 | Impulse Dynamics Pearl River, NY Regulatory Affairs Specialist BS/BA or MS in regulatory affairs Exp: 0-3 years |
Participate in preparation and submission of regulatory submissions to obtain approval to conduct domestic and international clinical investigations and to seek regulatory approval to commercialize the new and existing devices and their accessories. (IDE supplements, PMA, Annual reports, change notice etc) | 8/29/2020 |
| 10122 | InBios Seattle, WA Manufacturing Associate I - ELISA BS/BA in life sciences or Associates in applied sciences Exp: BS/BA: 0 years, Associates: 1 year |
If you have work experience in a GMP/ISO 13485 manufacturing facility and/or you have experience with PCR test-kit manufacturing please be sure to include that information on your resume or in a cover letter. If you would like to be part of a team responsible for the production of large-scale ELISA diagnostic test components in a BSL-2 laboratory, and you enjoy a busy workday under general supervision with daily goals working alongside a dedicated team that consistently meets deadlines and delivers products that meet high quality standards, then we encourage you to apply for this position. | 8/29/2020 |
| 10123 | Incyte Wilmington, DE Research Scientist, Biologics Analytical Sciences BS/BA or MS in sciences/engineering Exp: 1-3 years for analytical development for biologics |
Reporting to the analytical chemistry lead this position will be responsible for designing and conducting experiments to develop new analytical methods to support release testing, stability, and characterization of a growing biologics pipeline. This role requires scientific knowledge of a variety of analytical methods, experience in biologics development from early stage to late stage, and familiarity with ICH guidance. Strong interpersonal and communication skills are required. | 8/29/2020 |
| 10124 | Indivior Houston, TX Specialty Pharmaceutical Sales Rep/Clinical Specialist (Houston - North) BS/BA Exp: 1+ years in pharma/medical/healthcare |
The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. | 8/29/2020 |
| 10125 | InGeneron Houston, TX Quality Assurance Specialist BS/BA in biological sciences or engineering Exp: 0-3 years |
The Quality Assurance Specialist is responsible for providing Quality Assurance, Quality Control, and Preventative activity support for InGeneron’s Quality Management System. The Quality Assurance Specialist supports operations and other business functions with a focus on compliance to FDA and global quality system regulations and standards. | 8/29/2020 |
| 10126 | Innogenix Amityville, NY Quality Control Chemist MS in chemistry or related Exp: 1 year in QC |
Perform quality control/development activities. Develop, validate and test analytical methods. Analyze raw materials, in-process and finished product samples using modern QC techniques and advanced analytical equipment. Assist Scientists in developing/implementing quality systems and activities. | 8/29/2020 |
| 10127 | Inova Diagnostics San Diego, CA Research Associate I BS/Ba in biological sciences Exp: 1-2 years in research |
This position assists in the development of current and future Inova Diagnostic product lines by performing laboratory activities to assist in the development of new assays and/or the identification of potential new biomarkers. This position works under the supervision of the R&D management team and performs lab activities of limited scope, following good laboratory documentation practices and in accordance with Standard Operating Procedures and other Research and Quality System requirements. | 8/29/2020 |
| 10128 | Inova Diagnostics San Diego, CA Chemist I - Elisa Plates BS/BA in biological or chemical sciences Exp: 0-2 years in lab |
Assists with preparation of ELISA and Luminex™ plates according to established procedures. Major duties include assistance with reagent formulation, filtration and ELISA Plate Manufacturing activities. Assists with preparation of antigen solutions and buffers for ELISA plates according to written manufacturing documents. | 8/29/2020 |
| 10129 | Inova Diagnostics San Diego, CA Customer Service Representative I HS Diploma/GED Exp: 0-1 years |
Assists with answering phones and the processing of orders. Assists in answering the telephone. Assists Quality Assurance (QS) and Marketing with various projects. Assists in the processing, double checking and obtaining confirmation of sales orders. Assists in the preparation of paper work for the shipment of sales orders domestic and foreign | 8/29/2020 |
| 10130 | INOVIO San Diego, CA Associate, Quality Assurance (Laboratory) Associates or BS/BA Exp: 1-2 years in quality |
The Quality Assurance (QA) Associate (Laboratory) has the primary responsibility for supporting QA activities along with supporting Quality Systems and compliance as needed. The QA Associate performs a wide variety of duties, including supporting the daily QA Bioanalytics (laboratory) departmental operations, aiding with study protocol and report oversight, performing audits (internal/external) and performing various types of documentation reviews for applicable programs involving Inovio studies. | 8/29/2020 |
| 10131 | INOVIO San Diego, CA Research Associate I (Temporary/Contractor) BS/BA in biological sciences Exp: 0-1 years in lab |
The Research Associate I (RAI) works under general and specific direction in performing a spectrum of techniques in both cell culture and immunology. The RAI works collaboratively and independently in the lab, solves problems, completes required documentation, and performs general lab duties. | 8/29/2020 |
| 10132 | ConforMIS Wilmington, MA CNC Machinist, 1st Shift HS diploma or equivalent Exp: 1-3 year(s) |
The CNC Machinist I will be responsible for operation of CNC machining centers and polishing of medical implants in a high-volume manufacturing environment. Essential Duties and Responsibilities: Develop and maintain strong internal working relationships across Conformis. Understand the objectives, responsibilities, and mission of the operations department and work towards those goals. Prioritize and plan work activities; adapt for changing conditions. Operation and light maintenance of CNC machining centers and associated tooling. Perform hand de-burring of metal medical implants after machining. Perform in-process inspection of CNC machined parts. Perform timely and accurate transactions of workflow in ERP system. Maintain CNC machine spare parts and consumable tooling. etc. | 9/7/2020 |
| 10133 | Contract Pharmacal Corp Hauppauge, NY QA Manufacturing Coordinator AS/AA/BS/BA Exp: 1 year |
The QA Manufacturing Coordinator has primary responsibility for handling all front office operations as outlined below. Responsibilities: Including but not limited to: Track Change Controls and Deviations that affect manufacturing particularly those that affect MMR(s) and batch records. Change control assignee within Master Control all CC throughout all departments. Coordinate the bulk label process including creation, customer approval and maintenance. Liaison between Coating and QC, reporting batches completed through compression. Perform check of all issued batches to Manufacturing. Review issued commercial batches for coating material needs/maintain Coating Batch Log. Review of various Manufacturing systems (e.g. pest control, purified water). etc. | 9/7/2020 |
| 10134 | Cook Group West Lafayette, IN Research Engineer BS in engineering Exp: 1-5 year(s) |
The Research Engineer at Cook Research Incorporated is responsible for completing project deliverables and tasks to support the evaluation of novel design concepts for new medical products and providing support to projects in development at Cook Group companies. The successful candidate will support research and development of novel medical devices supporting the MedSurg Division for Cook. This candidate will also be expected to work with a project team to identify clinical needs, formulate new concepts, produce prototypes, conduct feasibility assessments and produce documentation for designs. Familiarity with a variety of medical device materials would be advantageous. etc. | 9/7/2020 |
| 10135 | Cook Group Poway, CA Machine Operator HS diploma or equivalent Exp: 6 months |
The Machine Operator at K-Tube Technologies will be skilled in operating machinery in one or more departments of Weld, Plug, Sink, Straightening, Cutting, Chop Cut, and CG. Knowledgeable in performing set ups in accordance with established procedures. Trained in the proper use of tooling for small, medium or large gauge sizes. Will also be responsible for the maintenance of all tooling used in manufacturing. Instructed in sampling procedure and inspection techniques on measuring the OD, using OD gauge and pin gauge for measuring ID. Must be certified to operate a machine and sign off on production. Performs process checklist and sampling procedure. etc. | 9/7/2020 |
| 10136 | Cook Group Pittsburgh, PA Equipment Associate HS diploma or equivalent Exp: 1-3 year(s) |
The Equipment Associate at Cook MyoSite assists in supporting company operations by monitoring and controlling laboratory equipment and production related utilities, as well as assisting with facility related aspects of equipment and the quality system. Responsibilities: Perform the proper receiving, tracking and storing of purchased equipment. Organize and maintain a calibration schedule for equipment. Ensure that all measuring and test equipment used is registered, assigned and marked with a unique internal equipment number for identification. Organize files and maintain all laboratory equipment and facility records. Maintain a calibration schedule utilizing calibration database software. etc. | 9/7/2020 |
| 10137 | CRISPR Therapeutics Cambridge, MA Research Associate, Genomics BS in biology or related Exp: 1+ year(s) |
We are seeking a Research Associate to join our next generation sequencing (NGS) wet lab. The successful candidate will be responsible for performing quality control experiments and generating NGS data to support the development of novel genetic therapies for a serious diseases. This position requires enthusiasm, attention to detail, and a desire to create new medicines for patients. This position reports directly to the head of the NGS wet lab. General Responsibilities: Perform routine quality control experiments on sequencing libraries (fluorescent quantification, capillary electrophoresis, and qPCR) and prepare samples for sequencing. Load and operate Illumina sequencers. Apply operational knowledge of instruments used in the genomics space (e.g. TapeStation, Bioanalyzer, optical plate reader, robotic liquid handling, and Illumina sequencers). etc. | 9/7/2020 |
| 10138 | CSL Dallas, TX Plasma Lab Technician HS diploma or equivalent Exp: 3+ months |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. Ensures accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. May ensure samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. etc. | 9/7/2020 |
| 10139 | CSL New Hope, MN Customer Service - Donor Support Technician HS diploma or equivalent Exp: 3+ months |
Responsible for preparing the donor, donor area and equipment for the pheresis process. Job Description: Main Responsibilities: Prepares the autopheresis machine for the pheresis process. Monitors the donor and the pheresis process, responds to specific alarms or signals that may occur during the process. Disconnects the donor when the process is complete. Maintains alertness and awareness to any reaction donor may have during or after the pheresis process and notifies appropriate staff. Uses Personal Digital Assistant (PDA) to record incidents that occur during the pheresis process, such as machine alerts and alarms, volume variances and donor adverse events. etc. | 9/7/2020 |
| 10140 | CSL Burlington, NC Medical Screener - Reception Technician (Customer Service) HS diploma or equivalent Exp: 3+ months |
Responsible for greeting donors at the plasma collection center and conducting a series of registration procedures to verify donor suitability for the plasma pheresis process. In compliance with Standard Operating Procedures (SOPs), assists qualified donors in completing the screening process. The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the donation process, referring donors to medical staff when appropriate and performing health screening procedures such as blood pressure, pulse, weight, temperature. Performs finger stick to obtain sample to obtain donor’s hematocrit and total protein levels. etc. | 9/7/2020 |
| 10141 | CSL Madison, TN Medical Screener - Reception Technician (Customer Service) (Bilingual – English/Spanish) HS diploma or equivalent Exp: 3+ months |
Responsible for greeting donors at the plasma collection center and conducting a series of registration procedures to verify donor suitability for the plasma pheresis process. In compliance with Standard Operating Procedures (SOPs), assists qualified donors in completing the screening process. The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the donation process, referring donors to medical staff when appropriate and performing health screening procedures such as blood pressure, pulse, weight, temperature. Performs finger stick to obtain sample to obtain donor’s hematocrit and total protein levels. etc. | 9/7/2020 |
| 10142 | CSL Manhattan, KS Customer Service - Donor Support Technician HS diploma or equivalent Exp: 3+ months |
Responsible for preparing the donor, donor area and equipment for the pheresis process. Job Description: Main Responsibilities: Prepares the autopheresis machine for the pheresis process. Monitors the donor and the pheresis process, responds to specific alarms or signals that may occur during the process. Disconnects the donor when the process is complete. Maintains alertness and awareness to any reaction donor may have during or after the pheresis process and notifies appropriate staff. Uses Personal Digital Assistant (PDA) to record incidents that occur during the pheresis process, such as machine alerts and alarms, volume variances and donor adverse events. etc. | 9/7/2020 |
| 10143 | CSL Evansville, IN Medical Screener - Reception Technician (Customer Service) HS diploma or equivalent Exp: 3+ months |
Responsible for greeting donors at the plasma collection center and conducting a series of registration procedures to verify donor suitability for the plasma pheresis process. In compliance with Standard Operating Procedures (SOPs), assists qualified donors in completing the screening process. The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the donation process, referring donors to medical staff when appropriate and performing health screening procedures such as blood pressure, pulse, weight, temperature. Performs finger stick to obtain sample to obtain donor’s hematocrit and total protein levels. etc. | 9/7/2020 |
| 10144 | CSL Hamilton, NJ Sr Plasma Processing Technician HS diploma or equivalent Exp: 3+ months |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. Main Responsibilities: In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. etc. | 9/7/2020 |
| 10145 | Cutis Pharma Woburn, MA Quality Control Chemist--Entry Level BS/BA Exp: 0-1 year(s) |
The QC Chemist will be responsible to perform assigned tasks accurately, following approved documents, Azurity Pharmaceuticals procedures and policies, Good Documentation Practices, and Good Analytical Laboratory Practices. PRINCIPAL DUTIES AND RESPONSIBILITIES: Perform analytical testing of API and finished products. Instrumental analysis and wet chemistry. Demonstrate familiarity with standard QC lab equipment. Independently collect, analyze, and interpret data and recognize aberrant results. Maintain good housekeeping in QC Lab. etc. | 9/7/2020 |
| 10146 | Cutis Pharma Wilmington, MA Quality Line Inspector BS/BA in chemistry or a life science Exp: 1-3 year(s) |
DUTIES & RESPONSIBILITIES: Inspect all incoming component shipments to ensure that all applicable specifications are met. Inspect product shipments coming from contract manufacturers/repackagers to ensure that all necessary components meet quality standards. Help trouble-shoot packaging concerns and communicate with contract manufacturers/ repackagers and vendors. Verifies and inspects incoming materials and works accordingly with Quality Assurance to handle any possible discrepancies. Participates in other quality audits when required. Complete and maintain documentation of all items inspected and findings/conclusion of findings. Provide oversight on production line; assist Production Technicians with questions/inquiries about products. etc. | 9/7/2020 |
| 10147 | Cytek Biosciences Fremont, CA Research Scientist I BS/MS in a life science Exp: 1-2 year(s) |
We are seeking a motivated candidate who can assist in new reagent, assay, and system development and testing. The candidate should be able to execute experiments and testing independently following protocols or instructions. In addition, the candidate should have good communication, documentation and problem-solving skills. Primary Responsibilities: Follow instructions to carry out flow cytometry experiments using biological samples. Follow SOPs and protocols to carry out reagent, assay panel, and instrument testing. Perform data analysis and summarize data for review. Design experiment to trouble shoot if necessary. etc. | 9/7/2020 |
| 10148 | Cytek Biosciences Columbus, OH Flow Cytometry Field Service Engineer BS in a life science or engineering Exp: Not required |
DUTIES AND RESPONSIBILITIES: Install, troubleshoot and repair flow cytometers and Cytek Upgrade products with proficiency in a timely manner. Work professionally and courteously as an individual with Cytek’s customers in continuous support of Cytek’s reputation of service excellence. Identify customer needs and contribute to improvements in Cytek products. Manage the daily schedule to ensure appropriate priority is placed upon urgent customer needs while setting customer expectations for issues of less urgency. Customer Management through telephone technical support, service visit scheduling, product problem information gathering, fault isolation, corrective action, and site visit closure with high quality and efficiency. etc. | 9/7/2020 |
| 10149 | Cytek Biosciences Seattle, WA Flow Cytometry Field Service Engineer BS in a life science or engineering Exp: Not required |
DUTIES AND RESPONSIBILITIES: Install, troubleshoot and repair flow cytometers and Cytek Upgrade products with proficiency in a timely manner. Work professionally and courteously as an individual with Cytek’s customers in continuous support of Cytek’s reputation of service excellence. Identify customer needs and contribute to improvements in Cytek products. Manage the daily schedule to ensure appropriate priority is placed upon urgent customer needs while setting customer expectations for issues of less urgency. Customer Management through telephone technical support, service visit scheduling, product problem information gathering, fault isolation, corrective action, and site visit closure with high quality and efficiency. etc. | 9/7/2020 |
| 10150 | Cytovance Biologics Oklahoma City, OK SOLUTION PREP ASSOCIATE AS/AA in a life science Exp: 1-2 year(s) |
This position is accountable for producing and delivering large and small-scale media and buffers to support Upstream and Downstream Manufacturing Operations. ESSENTIAL DUTIES AND RESPONSIBILITIES: Batching and delivering both large and small-scale media and buffer batches. Assisting in the review & creation of operation documents by providing input to technical composition of documents. Effectively demonstrate understanding of GMPs & how it applies to specific responsibilities. Following accurate oral & written procedures in operating production equipment & performing processing steps. Maintain orderliness of process area. etc. | 9/7/2020 |
| 10151 | Cytovance Biologics Oklahoma City, OK MANUFACTURING ASSOCIATE - UPSTREAM - NIGHT SHIFT AS in science or biotechnology Exp: 1-2 year(s) |
Executes upstream manufacturing of clinical and commercial products. Executes pre and post processing activities such as: clean of production equipment, including the operation of automated bioreactor, harvest and media prep skids. This position is accountable for executing the manufacturing processes in Contract Manufacturing Facility and/or Master Cell Banking Facility. ESSENTIAL DUTIES AND RESPONSIBILITIES: Ability to work with bioreactor operation and cell culture including aseptic technique. Execute and monitor critical processes supporting mammalian, microbial, and fill finish production facilities. Solid experience with the following: large-scale centrifuges, washers, autoclaves. etc. | 9/7/2020 |
| 10152 | Cytovance Biologics Oklahoma City, OK MANUFACTURING ASSOCIATE - DOWNSTREAM AS in science or engineering Exp: Not necessary for AS candidates |
This position is accountable for the execution of procedures for purification manufacturing and support area of manufacturing using SOP’s and batch records. Operating production equipment for purification that may include process monitoring, purification and formulation. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform in-process testing where applicable. Interface with Quality Control department to submit in-process samples and coordinate environmental monitoring during key process steps. Provide support to cross-functional teams to meet production or timeline demands. Demonstrate understanding in scientific concepts, technical operations, safety, and Good Manufacturing Practice. Provide suggestions for process optimization and efficiency, where applicable. etc. | 9/7/2020 |
| 10153 | Day Zero Diagnostics Boston, MA Laboratory Research Associate BS in molecular biology, biochemistry, or microbiology Exp: 1 year |
Job Duties: Perform and assist with sample processing toward diagnostic workflows. Ensure quality control of equipment, reagents, and clinical samples. Strictly follow all lab procedures for specimen handling, processing, and reporting. Maintain meticulous documentation of experimental outcomes and observations. Work closely with Research Scientists and Associates and maintain close communication with direct supervisor. Repetitive workflows are a frequent occurrence. etc. | 9/7/2020 |
| 10154 | Demetrix Berkeley, CA Associate Scientist/Sr. Associate Scientist - Analytical Chemistry BS in chemistry, biochemistry, chemical engineering, or related Exp: 1 year |
You will be part of an interdisciplinary team of fermentation scientists and engineers, automation engineers, software engineers, analytical chemists, and molecular biologists to rapidly develop microbial strains to produce high value natural product medicines. The Analytical Chemistry group is an integral part of the Demetrix team, providing the rest of the company with high quality data while maintaining and balancing accuracy, precision, and throughput. As part of the Analytical Chemistry group, you will help us with operations, instrument maintenance and troubleshooting, and development of new methods while fostering an atmosphere of continued improvement and innovation. etc. | 9/7/2020 |
| 10155 | Dexcom San Diego, CA Engineering Technician 1 HS diploma or equivalent Exp: 0-2 years |
As a member of the R&D Advanced Technology team this Technician will support efforts to understand current and future needs of our manufacturing and automation processes, explore and evaluate new technologies and concepts for meeting those needs, and assist in rapidly demonstrating feasibility of such technologies through rigorous modeling, analysis, prototyping, experimentation, and other risk identification and mitigation activities. Functional Description: Supports engineering activities such as design, test, check-out, modification, fabrication and assembly of prototype electro mechanical systems, experimental design circuitry, laser/light transmission devices or specialized test equipment. Applications may include electronic circuits, photonics and logic systems. etc. | 9/7/2020 |
| 10156 | Dyne Therapeutics Waltham, MA Research Associate/Senior Research Associate - Biology BS/MS in a biological discipline Exp: 1-2 year(s) |
Dyne is seeking a talented and highly motivated Research Associate/Senior Research Associate to join our drug discovery team. This member will work closely with other researchers to develop biomarker assays using a variety of innovative technologies. The successful candidate will be ambitious, motivated, an energetic self-starter who enjoys working in a fast-paced environment. We offer a competitive salary with benefits and an opportunity for learning and advancement in an exciting innovative environment. Primary Responsibilities Include: Execute research plans for in vitro/in vivo studies. Analyze data and communicate findings to team members and management. etc. | 9/7/2020 |
| 10157 | Holologic San Diego, CA Research Associate 2 BA/BS in molecular biology, chemistry, or biochemistry Exp: 0-2 years |
Hologic is seeking a Research Associate 1 or 2 responsible for designing and performing experiments while collaborating and communicating effectively. Essential Duties and Responsibilities: The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Performs minimally complex experiments with input from supervisor. Understands experimental goal and may provide input to the experimental design. Analyzes data from individual experiment with input from supervisor and documents work in laboratory notebook or report. Able to summarize a group of experiments. Effectively communicates with peers and supervisor. May present data in group meetings. etc. | 9/7/2020 |
| 10158 | Holologic San Diego, CA Research Associate 1 or 2 BA/BS in molecular biology, chemistry, or biochemistry Exp: 0-2 years |
Hologic is seeking a Research Associate 1 or 2 responsible for designing and performing experiments while collaborating and communicating effectively. Essential Duties and Responsibilities: The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Performs minimally complex experiments with input from supervisor. Understands experimental goal and may provide input to the experimental design. Analyzes data from individual experiment with input from supervisor and documents work in laboratory notebook or report. Able to summarize a group of experiments. Effectively communicates with peers and supervisor. May present data in group meetings. etc. | 9/7/2020 |
| 10159 | Editas Medicine Cambridge, MA Clinical Trial Assistant BA/BS Exp: 1-3 year(s) |
The Clinical Trial Assistant is an individual contributor providing clinical trial coordination support, along with implementing the clinical operational plans in accordance with regulatory guidelines and ICH/GCP standards. The Clinical Trial Assistant will be responsible for providing Clinical Operations support of study specific reports and site and vendor management activities. throughout the full lifecycle from study start-up through database archive. This includes collaboration with CROs and cross-functional teams. The position reports to the VP Clinical Science Operations and Clinical Quality. These responsibilities include: Supports the clinical team in the overall management of studies, including planning, execution and closeout of one or more clinical trials. etc. | 9/8/2020 |
| 10160 | Elpis Biopharmaceuticals Lexington, MA Research Associate, Biology & Functional Assays BS/MS in biology, biochemistry, molecular biology, immunology, or related Exp: 1-3 year(s) |
We are looking for a research associate to joint the biology and functional assay group. This group will analyze and screen newly discovered therapeutic molecules for biochemical, cellular and immunological function. The candidate will be responsible for efficiently delivering high-quality research results for decision making. The candidate will also help explore and develop innovative technologies to advance biologic projects. The candidate will analyze scientific results, provide oral and written reports, and remain current to literature reports and technological developments. etc. | 9/8/2020 |
| 10161 | Emergent Biosolutions Baltimore, MD Manufacturing Associate BS in biological sciences or HS diploma Exp: 1+ year(s) |
The Manufacturing Associate II position reports to Manager Manufacturing at Emergent Manufacturing Operations Baltimore (EMOB). Prior experience in GMP manufacturing and operation of GMP process equipment are prerequisites. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Operates manufacturing equipment such as: incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in process testing equipment. Demonstrates, understands and adheres to Emergent policies, GMP standards and safety procedures. Informs Manager on progress of projects, transfer of data, process details, etc. | 9/8/2020 |
| 10162 | Emergent Biosolutions Baltimore, MD Manufacturing Associate (Upstream) BS in biological sciences or HS diploma Exp: 1+ year(s) |
The Manufacturing Associate II position reports to Manager Manufacturing at Emergent Manufacturing Operations Baltimore (EMOB). Prior experience in GMP manufacturing and operation of GMP process equipment are prerequisites. ESSENTIAL FUNCTIONS: Operates manufacturing equipment such as: incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in process testing equipment. Demonstrates, understands and adheres to Emergent policies, GMP standards and safety procedures. Informs Manager on progress of projects, transfer of data, process details, etc. Executes batch records according to GMP and site quality standards. etc. | 9/8/2020 |
| 10163 | Emergent Biosolutions Lansing, MI Analyst I, QC Environmental Monitoring BS in an applied science Exp: 0-2 years |
This is a laboratory testing position with the major responsibilities being daily routine testing and laboratory maintenance tasks. Additional responsibilities involve quality systems support. ESSENTIAL FUNCTIONS: Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Environmental Monitoring Responsibilities: Perform general laboratory duties including, but not limited to: Clean laboratory areas/glassware. Biosafety Cabinet Monthly Cleaning. Safety equipment upkeep including eyewash stations. Transfer and dispose of biohazard waste and chemicals. etc. | 9/8/2020 |
| 10164 | Emergent Biosolutions Baltimore, MD Analyst II, QA Raw Materials BS/MS in chemistry or biology Exp: 1-3 year(s) |
The QA Analyst II is responsible for performing duties related to raw materials review and release for the CGMP operation of Emergent BioSolutions Emergent BioSolutions at the Baltimore Camden Site. Our QA Department provides expertise in problem solving and process improvements. The QA Analyst will interact with all departments to provide guidance necessary to maintain and improve CGMP compliance at the company. ESSENTIAL FUNCTIONS: Raw Materials: Perform critical reviews of Incoming material documentation submitted for QA disposition. Perform activities associated with the Active Pharmaceutical Ingredient (e.g. receipt, inspection and document review). etc. | 9/8/2020 |
| 10165 | Encoded Therapeutics South San Francisco, CA Research Associate I/II, In Vivo Research MS in biosciences Exp: 0-2 years |
We are recruiting a highly motivated researcher to join our team. This is a unique opportunity to work at the intersection of genomics and therapeutics and participate in the development of a diverse therapeutic pipeline driven by a transformative core technology. The successful candidate will work well across multiple projects in a fast-paced and dynamic environment. Requirements: Conduct in vivo procedures to evaluate efficacy of AAV gene therapy candidates in rodent models, primarily mice. Perform standard mouse procedures including plasma/serum collection, IV injections, necropsies, and tissue collection in compliance with established protocols. Conduct in life safety assessments: monitor body weight, clinical observations, and survival of mice. etc. | 9/8/2020 |
| 10166 | EntroGen Woodland Hills, CA Quality Control/Quality Assurance Associate BS/MS in molecular biology, biology, biochemistry, or related Exp: 1+ year(s) |
EntroGen is seeking a Quality Control/Quality Assurance Associate who will be responsible for routine quality control procedures under general supervision. The main responsibilities of this position include performing routine testing of raw materials, in-process samples, controls, and finished product, writing protocols and reports, compiling data into comprehensive packages, packaging and inspecting products, reviewing batch records for accuracy, assuring cGMP compliance, and writing/revising SOPs. This position will also provide support to manufacturing and production as needed. etc. | 9/8/2020 |
| 10167 | Envigo Alice, TX Animal Care Technician Unspecified Exp: 6-12 months |
To assist with daily primate husbandry in accordance with SOPs and assist with maintenance of work area. How you will contribute to make a difference: Perform daily rounds to observe primates for signs of illness. Perform routine weighing of primates. Capture and restrain primates as needed. Maintain and sanitize animal enclosures. Assist with administration of medications. Perform blood collections. Perform documentation as required by operating procedures. Conduct general animal husbandry procedures. Assist in preparing and crating primates for incoming or outgoing shipments. Outside maintenance, grounds keeping. etc. | 9/8/2020 |
| 10168 | Erytech Princeton, NJ Technician - Manufacturing BS in a biological science Exp: 1-2 year(s) |
Scope: Be able to manufacture human blood derived oncology drugs per Standard Operating Procedures in a controlled cleanroom environment. Ensures all manufacturing activities are performed under cGMP guide lines. Communicates production deviations/incidents to the supervisor/Manager as soon as it is discovered. Responsibilities: Ensures all training requirements are completed according to Erytech training guidelines. Perform all manufacturing activities according to cGMP guide lines. Record all manufacturing activities in the batch record and Erycaps machine according to the SOP.ng. etc. | 9/8/2020 |
| 10169 | Eurofins Denver, CO Mold/Asbestos Analyst BS in microbiology, biology, geology, or related Exp: 1+ year(s) |
The Analyst primarily performs analysis of bulk samples using PLM for asbestos, and analysis of non-culturable surface and air samples for fungi. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and enters laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. etc. | 9/8/2020 |
| 10170 | Eurofins West Point, PA Downstream Process Development Scientist BS in biology, chemistry, or related Exp: 0-2 years |
Employee Responsibilities: Perform lab-scale downstream processing of vaccine products and process intermediates. Perform assays on vaccine products, process intermediates, and related experimental samples using biochemical/analytical tests. Prepare solutions/reagents. Set-up process equipment for lab-scale experiments. Maintain records and experimental results following good manufacturing practices (GMP). etc. | 9/8/2020 |
| 10171 | Exelixis Alameda, CA Assistant Research Scientist I BS/MS in a biological science Exp: 0-2 year(s) |
The successful and highly motivated candidate will support the clinical pharmacology and nonclinical development in PK data review and documentation in addition to contributing to the multidisciplinary development teams by designing and executing pharmacokinetics data transfer between Exelixis and external vendors. ESSENTIAL DUTIES AND RESPONSIBILITIES: Assist in the planning, design and implementation PK data transfer plans from external vendors to Exelixis and from Exelixis to external vendors. Perform quality check of preclinical and clinical PK/TK data and reports and PK sections of regulatory documents (IND, IB, and NDA). Work with PK scientists and multiple functions to perform PK data cleaning and reconciliation for clinical studies. Support archiving of the final preclinical DMPK and clinical PK data and reports. Perform literature search to support PK data analysis. etc. | 9/8/2020 |
| 10172 | Cayman Chemical Company Ann Arbor, MI Associate Scientist (Analytical Chemistry) MS in chemistry or related Exp: Not necessary for MS candidates |
We are currently seeking candidates for an Associate Scientist with the key duties and skills listed below: Duties and Responsibilities: Consistent compliance with and promotion of all Cayman values, policies, SOPs, and regulations including, but not limited to: Lab Notebook Policy. Safety and regulatory policies. Confidentiality policies. Timely, accurate data entry (AX, SharePoint, P-drive folders, Excel spreadsheets ). Perform assigned tasks with increasing independence: Operate and maintain HPLC, MS, GC, and optical rotation instrumentation. Perform analytical support services for internal chemists and external clients. | 9/1/2020 |
| 10173 | Celerion Tempe, AZ Clinical Research Coordinator BA/BS Exp: 1-2 year(s) |
We have an exciting opportunity for Clinical Research Coordinator to join our Tempe, AZ clinical team! As a you work closely with our clinic operations team to ensure the success of our phase one clinical trials, Research Coordinators interpret study protocols to generate needed source documents, they add time and event codes into our systems to account for the needed tasks in a trial, they coordinate needed supplies for a given study and ensure we are ready to deliver. A background in clinical research or health care is a plus, but it is not required. We are seeking someone with well honed critical thinking skills, an ability to manage multiple projects at once, and well-developed time management skills. | 9/1/2020 |
| 10174 | Celerion Tempe, AZ Entry-Level Project Coordinator (Clinical Research) BA/BS Exp: 1-2 year(s) |
We have an exciting opportunity for beginning project manager to join our Tempe, AZ clinical team! As a Clinical Project Coordinator you work closely with our clinic operations team to ensure the success of our phase one clinical trials. Project Managers interpret study protocols to generate needed source documents, they add time and event codes into our systems to account for the needed tasks in a trial, they coordinate needed supplies for a given study and ensure we are ready to deliver. A background in clinical research or health care is a plus, but it is not required. We are seeking someone with well honed critical thinking skills, an ability to manage multiple projects at once, and well-developed time management skills. | 9/1/2020 |
| 10175 | Celerion Tempe, AZ Research Laboratory Assistant -- FT -- 6AM-2PM Shift AS/BS in a laboratory life science Exp: 1+ year(s) |
Research Laboratory Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). We are specifically seeking candidates with laboratory sample preparation and/or biological sample processing experience. This is a full time position scheduled for 40 hours per week with weekend availability expected. This position is slated to start on September 14, 2020. | 9/1/2020 |
| 10176 | Celerion Tempe, AZ Fulltime Entry-level Lab Assistant BS in a laboratory science Exp: 1+ year(s) |
Research Lab Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). If you have recently graduated with a laboratory-based science degree (i.e. Biology, Microbiology, Chemistry) and are looking to begin fulltime work at a clinical site, we'd love to speak with you! | 9/1/2020 |
| 10177 | Celerion Tempe, AZ Research Laboratory Assistant -- FT --2PM-10PM Shift AS/BS in a laboratory life science Exp: 1+ year(s) |
Research Laboratory Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). We are specifically seeking candidates with laboratory sample preparation and/or biological sample processing experience. This is a full time position scheduled for 40 hours per week with weekend availability expected. This position is slated to start on September 14, 2020. | 9/1/2020 |
| 10178 | Celerion Tempe, AZ Research Laboratory Assistant -- FT --10PM-6AM Shift AS/BS in a laboratory life science Exp: 1+ year(s) |
Research Laboratory Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). We are specifically seeking candidates with laboratory sample preparation and/or biological sample processing experience. This is a full time position scheduled for 40 hours per week with weekend availability expected. This position is slated to start on September 14, 2020. | 9/1/2020 |
| 10179 | Celerion Tempe, AZ Entry Level Clinical Data Assistant (FT) AS/AA/BS/BA Exp: 1-2 year(s) |
We seek an eager data entry master to join our data management team at our Tempe, AZ Phase 1 Research Clinic. This is a great entry-level opportunity to begin a career in clinical data management. This is a fulltime position, working 40 hours per week with shifts occurring onsite between 9AM-5PM, Monday-Friday. Essential Functions: Perform accurate data entry and verification for study specific External Studies, Celerion Standard, Spondor Provided EDC, and Sponsor Provided Paper CRFs (if applicable). Work with Clinical Data Manager for External Studies to create a working copy of the completed paper CRFs to ensure accurate and consistent data entry. Collate source data and signed disposition pages into final CRFs. | 9/1/2020 |
| 10180 | Cell Signaling Technology Danvers, MA Research Associate - VSC BS in a biological science Exp: 1+ year(s) |
We are seeking a Research Associate to join our Validation Systems Core (VSC) team within our Product Development organization. The VSC serves as a centralized resource for innovation in the culture, treatment, lysis, and storage of cell lines. The Research Associate is responsible for providing well-characterized, high quality cells and lysates to the organization to support Product Development efforts focused primarily on affinity research reagents such as primary antibodies, in addition to other product types such as assay kits, conjugates, and ELISA pairs. This position is a dynamic role in a fun, fast paced environment. The VSC places emphasis on teamwork so candidates are expected to collaborate and work well with fellow group members. | 9/1/2020 |
| 10181 | Cell Signaling Technology Beverly, MA Filling & Assembly Specialist I - 6-Month Contract HS diploma or equivalent Exp: 1+ year(s) |
The Filling & Assembly Specialist I functions as a member of our Global Supply Chain team to support the discrete manufacturing of our products. Specifically, the Packaging team is responsible for filling and assembly of final products to ensure finished goods inventory is ready and available for customers. This is a temporary 6-month assignment, with hours from 8 AM – 4 PM, Monday – Friday, 37.5 hours per week. Responsibilities: Precision aliquoting and filling of antibody products utilizing liquid handling techniques with strict adherence to SOPs to ensure product quality. Labeling of vials and preparation of packaging for component assembly, adhering to strict quality control guidelines to ensure labeling and packaging meets compliance requirements and standards. Inspecting and packaging product components with manual and/or automated systems to create final products for order fulfillment. Set-up, change-over and operation of labeling, pumping and packaging equipment. Data entry and updating to enable accurate inventory records. | 9/1/2020 |
| 10182 | Cell Signaling Technology Danvers, MA Research Associate - Purification BS in cell biology, biochemistry, or chemistry Exp: 1-2 year(s) |
We are seeking a Research Associate to join our Purification team. S/he will assist with the purification of antibodies using Protein A and peptide affinity chromatography. The successful candidate should have basic knowledge of laboratory experience, good communication skills and be highly collaborative. Responsibilities: Benchtop purification as well as purifications performed robotically. Responsibilities for this position will also include inventory management, data entry and solution preparation. Researches and identifies opportunities for process and protocol improvements. Effectively follows SOPs and produces consistent results and throughput metrics. Stays current with scientific research and demonstrates a willingness to learn new skills and techniques. Mentor and guides others in scientific and technical matters. Can direct the efforts of others (e.g. summer interns) on small projects with assistance. | 9/1/2020 |
| 10183 | Cellular Dynamics Madison, WI Laboratory Technician AS/AA in a relevant science discipline Exp: Not necessary for AS/AA candidates |
FUJIFILM Cellular Dynamics, Inc is recruiting for a laboratory technician to work in our cell manufacturing and research facility in Madison, WI. This role provides an outstanding opportunity for a dedicated and responsible individual to contribute to maintaining and improving the operations in our facility. Ideal candidates can demonstrate a track record of self-motivation, strong organizational skills, and dedication to their work. Essential Job Functions: Provide lab support for scientific personnel and overall operations. Place orders, maintain inventory, and stock laboratory supplies. Work with laboratory staff to maintain and mature organizational structure. Organize and put away daily shipments consistent with inventory management, housekeeping and safety standards. Perform maintenance on equipment as specified, including minor repairs and cleaning. | 9/1/2020 |
| 10184 | Celsius Therapeutics Cambridge, MA Research Associate II, Immuno-Oncology, Target ID and Validation MS Exp: 1-3 year(s) |
We seek a passionate and committed bench scientist to join our team with a focus on oncology and immuno-oncology target validation. The successful candidate will have a sound understanding of cell biology and extensive experience with in vitro assay development. We’re looking for candidates excited by the opportunity to interrogate targets identified through single-cell genomics and functional genomics efforts. RESPONSIBILITIES: Develop in vitro assay systems involving primary mouse and human immune cells to execute on target validation plans. Evaluate mechanistic role of candidate targets using a variety of perturbation approaches, such as CRISPR, RNAi, and pharmacological tools. Flexibly deploy different analysis techniques to address experimental goals (e.g. FACS, qPCR, ELISA, ). | 9/1/2020 |
| 10185 | Celsius Therapeutics Cambridge, MA Research Associate II, Autoimmune biology, Target ID and Validation MS Exp: 1-3 year(s) |
We seek a highly motivated bench scientist to focus on autoimmune target ID and validation. The successful candidate will have good prior experience in immune biology, with experience in assay development using immune cell types, including primary cell assays. Using this expertise, the successful candidate will gain experience learning how to apply large single cell and other datasets, as well as functional genomics approaches, towards the identification and validation of new targets. RESPONSIBILITIES: Develop and execute in vitro immune cell assays to functionally validate novel targets. Participate in the interrogation of single cell datasets towards the identification of novel autoimmune targets (prior experience with single cell RNA sequencing is not required). | 9/1/2020 |
| 10186 | Centrillion Technologies Palo Alto, CA Mechanical Engineer - Instrumentation BS/MS in mechanical engineering Exp: 1-2 year(s) |
Centrillion is seeking a Mechanical Engineer to assist in the development of innovative genomic research instrumentation for performing various biochemical reactions and signal detection/analysis. Responsibilities: Work as part of a team driving products through their lifecycle including concept generation, prototyping, component and device assembly, extensive testing. Help generate creative solutions to design problems and demonstrate their feasibility by considering factors such as risk, reliability, manufacturability. Assist the Project Lead and other members of the Engineering Team in transitioning concepts into products using solid modeling tools, defining requirements, selecting materials and processes. Assist in request for quoting duties, interacting with suppliers and manufacturers, and documenting the development process. | 9/1/2020 |
| 10187 | Centrillion Technologies Palo Alto, CA Laboratory Technician BA/BS in molecular biology, chemistry, genetics, or related Exp: 1-2 year(s) |
Centrillion is seeking Laboratory Technicians for their research and development teams. These positions are in a fast-paced, start-up environment, interacting with R&D scientists from a variety of backgrounds, with a heavy focus on molecular biology and biochemistry. Lab technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. The selected individuals will be working in a support role toward the development of new genomics technologies. The candidate will work with multiple scientists to assist with a broad range of duties including making buffers, following protocols, developing or adapting new protocols for new needs. | 9/1/2020 |
| 10188 | Danaher Lodi, CA Manufacturing Engineering Technician II AA/AS Exp: 1-2 year(s) |
PRIMARY RESPONSIBLILITIES: Follows company specific Safety procedures/guidelines and Work Instructions. Support in the build, installations, setups and qualifying Robot, Robot End of Arm Tooling (EOAT), Sorting Station, Conveyors and manufacturing related equipment as assigned. Support in any design improvements and changes to Injection Molding system in manufacturing. Support in develop and maintain documentation, initiate and implement assigned change orders. Complete assigned tasks and provide information that supports qualification, such as design, documentation, implementation and validation execution of new/changed equipment or process. Ability to learn to utilize/interpret precision measurements tools. | 9/1/2020 |
| 10189 | Danaher Sunnyvale, CA Regulatory Affairs Specialist II MS in a life science or related Exp: 0-2 years |
ESSENTIAL JOB RESPONSIBILITIES: Responsible for regulatory project timelines and management of global regulatory submissions. Coordinate and prepare regulatory submissions to ensure compliance with international regulations and guidelines. Establish and review Regulatory Affairs priorities as they relate to department and company goals and objectives. Interact with global regulatory leaders and peers to expedite approval of pending registrations. Support internal and external departments to generate protocols and reports for registration purposes. Maintain a "focused urgency" as required by specific events. Recognize potential problems by actively reviewing and analyzing internal and external factors. Assess potential impact and/or applicability to other related areas. | 9/1/2020 |
| 10190 | Danaher Lodi, CA Injection Molding Technician AA/AS Exp: 1-2 year(s) |
The position will work with all phases of the Injection Molding on production floor, (Prefer Nessie and Yushin experience) from start- up of molds, troubleshooting, set up of molds, and assist in monitoring quality. Responsible for setting and adjusting machine controls according to established window parameters while troubleshooting “Quality Issues” during production runs. Help Identified and diagnose technical issues for a quick resolution and immediate response to avoid press down time. Ensure to follow SOP and WI procedure and log in all data require for process on each lot running; as well as following all safety precautions to perform all tasks on a safe environment. | 9/1/2020 |
| 10191 | Ceva Verona, WI Maintenance Technician II - Verona AA/AS Exp: 1 year |
The Maintenance Technician II is responsible for assisting the Facilities and Engineering Manager with the maintenance, quality, and upkeep of the manufacturing, testing, and animal holding facilities, and the equipment and utilities at each location, in support of the manufacture of biological products consistent with the corporate objectives and external, international, and federal regulatory requirements. Responsibilities and Key Duties: Perform preventive maintenance on HVAC, electrical, structural and other non-critical equipment. Assist in the execution of PMs on critical equipment. Perform non-scheduled maintenance, on all non-critical equipment, in a timely manner as requested via the MWO system. Review and document all repairs, alarms and PM activities according to applicable Standard Operating Procedures. | 9/1/2020 |
| 10192 | Charles River South San Francisco, CA Research Associate BS in neuroscience, pharmacology, biology, or related Exp: 1+ year(s) |
We are seeking an experienced Research Associate (biotechnical) for our Discovery site located in South San Francisco, CA. ESSENTIAL DUTIES AND RESPONSIBILITIES: Rodent surgeries. Microdialysis and the development and running of rodent behavioral tests in support of CRO activities. Involvement in the design of experimental protocols and procedures, running experiments, and analyzing data. | 9/1/2020 |
| 10193 | Charles River Wilmington, MA Technologist - IVB AA/AS in a biological science or related Exp: 1 year |
Job Summary: The following are responsibilities related to the Technologist - IVB in Wilmington, MA: Perform daily test article/substance administration, observation and recording of physical signs of species for contracted laboratory studies. Prepare cage tags and individual animal number tags; prepare and autoclave cages. Prepare data forms for routine study procedures. Assist with preparation of data forms for specialized study procedures. Record study parameters as required by protocol. Ensure adequate supply of dosage equipment during the course of study. Assist in ensuring adequate supply of additional study specified materials such as blood collection tubes. Assist in preparation of test agents. | 9/1/2020 |
| 10194 | Charles River Mattawan, MI Animal Research Technician - Animal Services BS/MS Exp: None necessary |
We are seeking an Animal Research Technician for our Animal Services Team located in Mattawan, MI. An Animal Research Technician is responsible for: performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality, administering substances to animals; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. The following are minimum requirements related to the Animal Research Technician position. | 9/1/2020 |
| 10195 | Charles River Malvern, PA Technician 1 Microbiology BS in biology or related Exp: 1+ year(s) |
We are seeking a Technician 1 Microbiology for our Biologics Testing Solutions site located in Malvern, PA. The responsibilities of this role will be specific to the Sterile Services division of the Microbiology department. The following are the responsibilities of the Technician 1 Microbiology: Performance of direct inoculation and membrane filtration sterility testing. Performance of direct inoculation and membrane filtration bacteriostasis and fungistasis testing. Growth promotion testing of sterility and other microbiological testing media. | 9/1/2020 |
| 10196 | Charles River Wayne, PA Technician 1 Virology BA/BS in biology or related Exp: 0-1 year(s) |
Under direct supervision, the laboratory technician will be responsible for performing basic daily laboratory tasks as they relate to the operations performed within the Virology Department. The following are responsibilities related to the Technician 1 Virology: Perform routine laboratory tasks related to Virology testing. Practice proper aseptic and sterile processes during cell culture. Perform calibration, monitoring and cleaning of laboratory and lab equipment. Maintain inventory of necessary supplies by ordering and / or preparing reagents, media and solutions. | 9/1/2020 |
| 10197 | Charles River Durham, NC Electron Microscopy Technician 1 AS/BS in biology or related Exp: 0-1 year(s) |
Perform basic Electron Microscopy sample preparation with minimal supervision. Participate in the documentation of all activities as required. May also assist with setting up study files, inventories, and sending reports and study materials. We are seeking an Electron Microscopy Technician I for our Safety Assessment site located Durham, NC. The following are responsibilities related to the Electron Microscopy Technician I: Log in samples and set up study files for each protocol. Trim tissue, process/embed both viral and tissue specimens with supervision. Prepare solutions/reagents, cut thick/thin sections on the ultramicrotome, and stain slides/grids. Copy and send reports, prepare delivery slips, and return materials to the client. Understand and conduct all processes in compliance with Good Laboratory Practice (GLP) regulations, corporate Standard Operating Procedures (SOP), and the protocol. | 9/1/2020 |
| 10198 | Charles River Charleston, SC Quality Control Associate BA/BS Exp: 1 year |
We are seeking a Quality Control Associate for our Microbial Solutions site in Charleston, SC. This role will, ensure the quality and integrity of product by testing incoming materials, excipients and final product. The Quality Control Associate will be responsible for the following: Ensuring the quality and integrity of product by testing PTS cartridges, Limulus Amebocyte Lysate (LAL), incoming materials, and excipients. Perform Crude Lysate recovery procedures during the Horseshoe Crab Bleeding Season (Summer Months). Long-Term Stability monitoring of samples. Using technical writing to perform investigations and complete exception records. Attention to detail in all aspects of work is essential. | 9/1/2020 |
| 10199 | ChemGenes Wilmington, MA Junior Chemist BS in chemistry Exp: Not necessary for BS candidates |
The job duties: Manufacture of DNA & RNA compounds. Assist Senior Chemists. Prepare test solutions, reagents and ability to carry out reactions, to produce specialized ultra pure DNA/RNA synthesis products. Operate rotary evaporators, chillers, Preform column chromatography: small scale (on the bench) & large scale. Follow SOPs of standard products; report any deviations to Senior Chemists. Communicate with QC & QA department to update/create certificates of analysis. Maintain timely documentation of work. Evaluate data & prepare technical reports. General lab maintenance as necessary. | 9/1/2020 |
| 10200 | CheminPharma Woodbridge, CT Associate Scientist, Medicinal/Synthetic chemistry BS/MS in synthetic chemistry Exp: 0-5 years |
The successful candidate will be an experienced chemist with state of the art knowledge of synthetic organic chemistry and will be a motivated, creative, hands-on laboratory scientist with the ability to interact effectively with team members and external customers. Major responsibilities will involve design, synthesis, purification, and characterization of novel chemical entities and the management of general chemistry lab operations under the direction of senior scientific staff. The qualified individual is expected to contribute to process development and scale-up of key intermediates. | 9/1/2020 |
| 10201 | ChemPacific Baltimore, MD Chemist MS in chemistry or organic chemistry Exp: 1 year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 9/1/2020 |
| 10202 | ChemPacific Baltimore, MD Budget Analyst MS in finance Exp: Not necessary for MS candidates |
Duties: Work under the Chief Financial Officer to coordinate accounting and financial operations of the company to project and plan future earnings and expenditures. Apply principles of business finance to analyze financial records and financial operations in order to determine accuracy of financial records, efficiency of operations and effectiveness of budget control and to estimate future revenues and expenditures. Provide strategic analysis and advice to senior management for strategic decision making for entering into joint venture projects with businesses both in China and the United States to set up new production facilities in China, and new warehousing facilities and wholesale outlets in the United States; and Prepare budget reports, as well as long term budget plans with cost analysis and fiscal allocation, and maintain budgeting systems with the company to provide control of expenditures for product development and new business acquisitions and ventures. | 9/1/2020 |
| 10203 | Clinlogix Lower Gwynedd, PA Clinical Project Assistant I AS/BS in business administration, a life science, or related Exp: 1 year |
The Clinical Project Assistant I role is an entry level position to the clinical research industry. This role requires organizational skills with a high attention for detail. The ability to work in a team environment, meet deadlines, and prioritize and balance work from multiple projects is necessary. Excellent verbal and written communication skills are essential. This position will support the Clinical Project Assistants II/Senior Clinical Project Assistants, Clinical Project Managers, Clinical Research Associates and other Study Team Members as a supporting role for ongoing clinical studies. The Clinical Project Assistant I position is an integral member of the clinical project team providing support and troubleshooting on various aspects of project. | 9/1/2020 |
| 10204 | Coda Therapeutics South San Francisco, CA Research Associate/Sr. Research Associate Ion Channel Assay Development BS/MS in cell biology Exp: 1-2 year(s) |
This position will manage a wide range of administrative and executive support related tasks and will be able to work independently with little or no supervision. Primary Responsibilities: Assay Development: Design and validate cell-based fluorescence and automated electrophysiology assays to support receptor lead selection. Compound Screening: Execute medium throughout compound screening and follow-up pharmacological evaluation of small molecules on lead chemogenetic receptors. Organization and Communication of Data: Analyze and communicate data in written and oral modalities in both informal and formal settings. Generate and manage meticulous method protocols, data, and analysis reports in a clear and highly organized fashion. | 9/1/2020 |
| 10205 | Codexis Redwood City, CA Research Assistant/Associate, Biotherapeutics Lead Discovery BS/MS in biochemistry, structural biology, bioengineering, or related Exp: 0-6 years |
Codexis seeks a highly motivated researcher to join the Biotherapeutics Lead Discovery group to support our efforts to engineer novel biotherapeutic proteins. We are looking for a scientific researcher proficient in protein biochemistry and analytical methods development. Successful candidates will be part of an interdisciplinary, dynamic and enthusiastic biotherapeutics discovery team responsible for implementing Codexis’ core technologies and delivering candidate biologics. Responsibilities include: In collaboration with cross-functional project team members, perform high-throughput (HTP) screening campaigns to support directed evolution of next-generation biotherapeutics. Express recombinant protein variants in E. coli or mammalian cells for in vitro profiling. Execute and troubleshoot assay protocols for protein characterization (e.g., biochemical, enzyme activity, and cell-based assays). Adapt assays for HTP screening. | 9/1/2020 |
| 10206 | Codiak Lexington, MA Manufacturing Associate, Internal Drug Product Manufacturing AS/BS in biology, chemistry, mechanical engineering, or related Exp: 1-3 year(s) |
The Manufacturing Associate, Internal Drug Product Manufacturing is a production position focused on the activities associated with a closed-RABS isolator drug product filling operation. The position will be heavily manufacturing floor-based during preparation and execution of drug product filling, inspection and labeling activities. This position will report to the Supervisor of Internal Drug Product Manufacturing and is expected to interact with Quality Assurance and Control, Facilities Operations and Materials Management groups. The position is based in Codiak’s new clinical manufacturing facility “CMF” in Lexington, MA. | 9/1/2020 |
| 10207 | Cognate Bioservices Memphis, TN QC Analyst I - BioAssay BS in a biological science Exp: 0-3 years |
ESSENTIAL DUTIES AND QUALIFICATIONS: Adheres to Standard Operating Procedures (SOPs) and good documentation practices to ensure data integrity and traceability. Perform cell based immunological in vitro methods (e.g., cytotoxicity, HLA-restriction, cell proliferation, ). Perform release testing utilizing a variety of techniques ranging from compendia assays like pH and osmolality to more complex assays like, but not limited to, proliferation and cytotoxicity. Be able to quickly learn various methods and participate in the troubleshooting of assays. Enters observations and results into the appropriate trending databases for periodic analysis and trending. | 9/1/2020 |
| 10208 | Compass Therapeutics Cambridge, MA Entry Research Associate - Immunology and IO BS/MS in immunology, molecular biology, biochemistry, or related Exp: 1-3 year(s) |
We are a clinical stage Biotech company located in Cambridge that has been steadily growing. We are looking for a self-driven Senior or Junior Research Associate to play a critical role in supporting the research and development of the Immunology Program. This position will assume a key role in developing and implementing novel immunological assays in support of our proprietary therapeutics through an innovative antibody engineering platform. The position will be developing immunological assays in both cell lines and primary cells for identification and prioritization of therapeutic targets for clinical development. | 9/1/2020 |
| 10209 | Compass Therapeutics Cambridge, MA Research Associate, Immunology BS/MS in immunology, molecular biology, biochemistry, or related Exp: 1-5 year(s) |
Our Immunology team is seeking a hands-on scientist at our Cambridge, MA site. This role will play a critical role in supporting the research and development of the Immunology Program. This position will assume a key role in developing and implementing novel immunological assays in support of our proprietary therapeutics through an innovative antibody engineering platform. The position will be developing immunological assays in both cell lines and primary cells for identification and prioritization of therapeutic targets for clinical development. The ideal candidate will have a proven track-record of developing creative and novel immunology-based assays for solving complex biological problems, as well as a broad understanding of therapeutic drug discovery and its applications, | 9/1/2020 |
| 10210 | Compass Therapeutics Cambridge, MA Research Associate, In Vivo Immunopharmacology BS/MS in immunology, cell biology, or related Exp: 1+ year(s) |
Our in vivo Immunopharmacology team is seeking a hands-on scientist at our Cambridge, MA site. This individual will perform animal studies and in vitro assays to evaluate the anti-tumor activity of novel protein biologics and drive their advancement into the clinic. Experience with immunological assays and in vivo work experience are required. Candidates with work experience using immuno-oncology mouse models are encouraged to apply. Practical knowledge of ex-vivo primary cell manipulations, tissue culture and immunoassays highly preferred. The Research Associate Scientist position is an entry-level position that leverages existing knowledge and technical expertise to conduct preclinical studies under supervision. | 9/1/2020 |
| 10211 | ConforMIS Wilmington, MA Manufacturing Engineer I BS/MS in engineering Exp: 1-3 year(s) |
The Manufacturing Engineer I will be responsible for the selection, development, qualification, and scale-up of production processes and equipment across different manufacturing departments. Process objectives are the high quality, high volume production of patient-tailored implants and associated instruments. Essential Duties and Responsibilities: Develop and maintain strong, internal working relationships across ConforMIS. Understand the objectives, responsibilities, and mission of the Operations department and works towards those goals. Prioritize and plan work activities; adapt for changing conditions. Initiation, execution, and documentation of IQ, OQ, & PQ activities. Optimization of manufacturing processes (5S) for Lean Manufacturing. | 9/1/2020 |
| 10212 | Bristol Myers Squibb New Brunswick, NJ Associate Scientist GQAST Pharma & Forensics BS/BA Exp: 1-3 year(s) |
The Associate Scientist will be involved in hands on laboratory testing of foreign matter samples associated with manufacturing investigations, product quality complaint samples, and suspect product samples using spectroscopic techniques (NIR, Raman and mid-IR), microscopy, and wet chemistry methods. This work will cover the entirety of the BMS commercial portfolio, including both biologics and small molecule assets. They will provide analytical support to Global Quality, Corporate Security, External Manufacturing, and Manufacturing Operations, and to both internal and external sites as required. Duties: Support manufacturing investigations through characterization and identification of extraneous/foreign matter samples using relevant analytical techniques (mid-IR, Raman, SEM/EDS, microscopy). | 8/26/2020 |
| 10213 | Bristol Myers Squibb Seattle, WA Senior Research Associate, Cell Therapy Process Technologies MS in biology, chemical engineering, or related Exp: 1+ year(s) |
DUTIES AND RESPONSIBILITIES: Develop automated scale down model platform for cell therapy process development. Develop automated unit operations for adoptive T-cell therapy manufacturing. Evaluation of cell therapy manufacturing prototype devices. Design and execute small and large-scale cell therapy process development experiments. Analyze data from flow cytometry, cell functionality, or chemical assays. Write technical documents including development reports, batch records, and Standard Operating Procedures. Train operators or other engineers and scientists. | 8/26/2020 |
| 10214 | Bristol Myers Squibb Manati, PR Microbiology Analyst BS in biology, biotechnology, medical technology, or microbiology Exp: 1 year |
Performs laboratory analysis or tasks following established procedures and in full compliance with current governmental regulations, official compendia and any other policy / regulation to generate reliable and timely results, to comply with releases due date, reducing cycle time, and providing internal / external customer satisfaction. Responsibilities: The analysis are: bacterial endotoxin, sterility test, bioburden / microbial limit, growth promotion, particulate matter to parenteral products, microbial identification, pH test , ,osmolality, ,density, protein concentration and other analysis related to the release of the products being manufactured. In addition do microbial analyses of: manufacturing utilities (i.e. water, clean condensate, compress air, nitrogen, ). | 8/26/2020 |
| 10215 | Bristol Myers Squibb Devens, MA Associate / Assistant Scientist BS/MS in chemical engineering, bioengineering, biology or chemistry Exp: 0-6 years |
The Associate/Assistant Scientist within the Biologics Development - Upstream group will participate in the development and optimization of upstream processes for production of biologics at different clinical stages. The successful candidate will participate in the execution of bench-scale experiments using high-throughput, shake flask, or bioreactor cell culture systems to improve cell culture processes. Under general direction, the position requires participation in the design and execution of experiments, interfacing mainly with other upstream and occasionally with downstream and analytical personnel to achieve process development objectives. A successful candidate will work effectively in a cross-functional process development team and also be able to work independently to accomplish overall project goals. | 8/26/2020 |
| 10216 | Bristol Myers Squibb New Brunswick, NJ Associate Scientist MS in biotechnology, immunology, cell biology, molecular biology or related Exp: Not necessary for MS candidates |
Responsible for assay development, validation and Good Manufacturing Practice (GMP) testing for early and late stage biopharmaceutical drug development programs by utilizing knowledge of GxP (Good x = Manufacturing/ Laboratory /Clinical Practices) and specialized equipment such as optical density plate readers, luminometers, cell counters, time-resolved fluorescence plate readers, imaging microscopy, and fluorescence-activated cell sorting, and experience with laboratory technique such as ELISA, mammalian cell culture, bioassay applications, and cell signaling pathways. Carry out assigned laboratory work and other functional duties. Maintain research and GxP notebooks documenting all laboratory work consistently and accurately. | 8/26/2020 |
| 10217 | Brooks South Plainfield, NJ Part-time Night Shift Laboratory Technician HS diploma/AS Exp: 1+ year(s) |
Our Lab Techs are: Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. etc. | 8/25/2020 |
| 10218 | Brooks South Plainfield, NJ Associate Bioinformatics Scientist BS/MS in bioinformatics Exp: 0-3 years |
Responsibilities: Perform data analysis and generate reports for customer projects. Develop novel algorithms and build customized pipelines for clinical service projects. Build LIMS workflows for operation service lines. Evaluate and identify optimal NGS data analysis solutions. Conduct literature search for various genomics research areas etc. | 8/25/2020 |
| 10219 | Brooks South Plainfield, NJ Lab Assistant HS diploma Exp: 1+ year(s) |
We are seeking a Lab Assistant to join our Next Generation Sequencing team. Responsibilities: Check inventory and replenish consumable sequencing supplies. Assist in sample sorting and properly distribute them. Maintain laboratory cleanliness. Document and track daily work flow. Help with logistics as needed. Prepare supplies and assist Associate Scientists. etc. | 8/25/2020 |
| 10220 | Brooks South Plainfield, NJ Associate Scientist I BS in a biological science Exp: 1+ year(s) |
The Associate Scientist position in our Next Generation Sequencing department is a great entry-level role with room for growth and advancement. If you have the desire to work in a casual yet results-driven environment that embraces innovation- then you’re just what we’re looking for! Responsibilities: Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. etc. | 8/25/2020 |
| 10221 | Essity South Glens Falls, NY RST Process Engineer Converting BS in paper science, chemical, mechanical, electrical or industrial engineering Exp: 1+ year(s) |
This role serves as the day-to-day owner of the machine processes and process control systems for the plant. Owns and manages the development of troubleshooting skills of the manufacturing professionals. Acts as a subject matter expert for the machine processes. Participates and/or leads in Continuous Improvement projects. Helps to identify and support projects that will improve productivity, waste, quality and safety performance on a long term basis. We’re looking for people who embody our values, aren’t afraid to challenge, innovate, experiment, and move at a fast pace. We’re always looking for ways to improve our products and ourselves. If this is you, we’d love to talk. etc. | 8/25/2020 |
| 10222 | BD Mannford, OK Assembler 2, General HS diploma or equivalent Exp: 1-3 year(s) |
Job Description: Commitment to Safety, by following site safety procedures and utilizing safety equipment as required for daily tasks. Uses batch record instructions, job aids, standard operating procedures, and product specifications to execute production activities. Maintains accurate documentation, records and logs in accordance with FDA (Food and Drug Administration), GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization). Ability to perform minor troubleshooting and problem solving in areas of set-up of equipment and processes. Ability to perform rework and re-packaging of materials as needed. Ability to work in teams to achieve operational goals while being engaged in the process. Communicating issues and concerns to lead or designee. Performs assembly by following released procedures. etc. | 8/25/2020 |
| 10223 | BD Columbus, OH Manufacturing Team Manager, Night Shift BS/BA Exp: Not required for BS/BA candidate |
Under the direct supervision of the Unit Manger and Product Line Leaders. Directs and manages shift activities for assigned operations to ensure compliance to cost, quality, safety, human resource and regulatory plans and requirements. Establish and implement programs designed to assure control of processes and products that meet or exceed established standards and specifications. Informs management of quality problems and solutions relative to FDA and ISO compliance. RESPONSIBILITIES: Manages shift activities to achieve an overall objective of continuous improvement in productivity, quality, cost, budget compliance and attainment of strategic objectives. As required monitor and coordinate all plant shift operations - - timely communicate issues to unit manager. etc. | 8/25/2020 |
| 10224 | BD Baltimore, MD Machine Operator 2 AS/AA Exp: 0 years |
Performs routine set up, operation, minor routine maintenance, preventative maintenance (PM) and troubleshooting of moderately complex/automated manufacturing equipment. Controls and adjusts machine settings. Inspects in-process parts to ensure consistent quality and removes defective product, packaging, and component material. Assists with root-cause analysis activities for process or product exceptions. Checks work using prescribed gauges, jigs and fixtures to measure close tolerances. May monitor quality in accordance with statistical process or other control procedures. Ensures accurate documentation of all relevant quality, safety, and maintenance documents. Identifies, troubleshoots, and resolves basic issues associated with the machine performance and/or product quality. etc. | 8/25/2020 |
| 10225 | BD Glens Falls, NY Manufacturing Team Member I Crosser 1st Shift HS diploma or equivalent Exp: Not required |
Performs any combination of tasks involved in the manufacture and assembly of medical devices. Job Description: Responsible for following safety policies and procedures. Responsible for following all required GMP’s and applicable manufacturing procedures. Perform a variety of duties to assemble all types and sizes of product, components, and sub-assemblies using a variety of standard and specialty assembly machines or hand operations. May be required to press, bond, solder, flare, strip, clamp, sand, weld, mount/takedown or inspect for appearance, gauging of parts by “no-go” or “go” gauges and set fixtures. etc. | 8/25/2020 |
| 10226 | BD Baltimore, MD Quality Engineer II (Operations) MS in engineering, a biological science, chemistry, or computer science Exp: 1 year |
DUTIES: Maintain International Organization for Standardization (ISO) and regional regulatory requirements. Key elements focus on multiple aspects of quality for product design, manufacturing (assembly and test), inspections and customer complaints throughout the product life cycle. Develop Device History Files and maintain in a manner consistent with regulatory requirements. Generate process/product quality information in the form of CTQ (Critical to Quality) indices, recommendations and solutions to emerging issues, to share with project team/operations/suppliers. Supports the coordinated integration of new products into Manufacturing / Operations. Ensures BD Diagnostic Systems divisional, departmental policies, procedures, practices and facilities are in compliance with all applicable regulatory policies. Understanding and coaching others on Quality Systems and procedures. etc. | 8/25/2020 |
| 10227 | BD El Paso, TX Quality Assurance Technician I AS/AA in quality, life sciences, or engineering Exp: 1 year for AS/AA candidates |
This position is critical to the accurate evaluation of incoming materials, component, subassembly and finished product quality. Responsibilities include inspection, analysis of results, determining final disposition of some product and detecting nonconforming conditions. The Quality Assurance Tech I is also responsible for working within an established framework of compliance and developing and/or implementing improvements to product quality and the quality system. Principal Accountabilities: Inspect incoming and in-process materials, for compliance with established quality specifications. Work with production, receiving, and materials personnel to accurately complete required testing and documentation, determine correct disposition, and apply correct status labeling. Update material disposition status in SAP. etc. | 8/25/2020 |
| 10228 | BD Sandy, UT Molding Machine Operator HS diploma or equivalent Exp: 1-2 year(s) |
Molding operator/technician is responsible for molding production in assigned area and minor maintenance activities on assigned presses. Job Responsibilities: Operate injection molding presses to supply downstream equipment with molded components including inspection of components and requesting technical support to maintain part quality. Conduct minor maintenance activities on assigned presses. Work with other molding team members to keep equipment running during breaks and call-outs. Operate multi cavity injection molding machines and auxiliary equipment to manufacture product which conforms to quality specifications, at the rated output. etc. | 8/25/2020 |
| 10229 | Cabaletta Bio Philadelphia, PA Cellular Immunology Senior Research Associate/Associate Scientist MS in biology Exp: Not necessary for MS candidates |
Reporting to a Senior Scientist, Cellular Immunology, we are seeking an experienced, motivated, and highly skilled Cell Biology Associate Scientist. Under scientific and technical supervision, the candidate will perform various cell-based assays and maintain cell lines to contribute to the discovery and development of novel therapeutics at Cabaletta. The position offers growth into additional areas such as translational research and molecular biology, immunology and cell therapy. The position involves both technical and operational responsibilities. etc. | 8/25/2020 |
| 10230 | Cabaletta Bio Philadelphia, PA Molecular Biology Senior Research Associate/Associate Scientist MS in biology Exp: Not necessary for MS candidates |
Reporting to the Senior Scientist, Protein Production and Molecular Cloning group, we are seeking an experienced and motivated Molecular Biology Associate. Under scientific and technical supervision, the candidate will design and produce molecular constructs to be utilized for vector development and protein production. The candidate will also engage in characterizing peptides and proteins, perform ELISAs (Luminex™), and other assays as needed. The position offers growth into additional areas such as cell biology and molecular biology, immunology, and cell therapy. The position involves both technical and operational responsibilities. etc. | 8/25/2020 |
| 10231 | Cambrex Longmont, CO Formulations Scientist BS Exp: 0-3 years |
We are seeking an Associate Scientist to support formulation design and development activities within the Formulation team. This role will be responsible for executing oral solid dosage formulation experiments for drug product process development and analytical testing to primarily support early stages of the CDMO projects. Responsibilities: Assists on formulation and drug product process development projects, with an emphasis on early stages of development. Conducts physicochemical characterization and pre-formulation activities. etc. | 8/25/2020 |
| 10232 | Cardiovascular Systems Pearland, TX Assembly Technician HS diploma or equivalent Exp: 1 year |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. etc. | 8/25/2020 |
| 10233 | Cardiovascular Systems ST. Paul, MN Assembly Technician HS diploma or equivalent Exp: 1 year |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. etc. | 8/25/2020 |
| 10234 | Zoll Remote, IL Field Technician AS/AA Exp: Not necessary for AS/AA |
Responsible for providing onsite product support to specific customer accounts typically by contract. Product support consists of logistics, deployments, on-site trouble-shooting of product, preventative maintenance (PM) and software upgrades. Essential Responsibilities: Product support on-site and via telephone. Assist customer with application of equipment. Escalates customer related issues to Service Manager and CQA Regional Manager. Performs trouble-shooting on-site and corresponds with ZOLL Tech support staff to document the details related to the service and support activity. Performs on-site PM’s for service agreement devices / accounts. Potential for deployments or PM’s to other customers in region at the direction of the Manager. Able to maintain customer specific information related to service activity. etc. | 8/26/2020 |
| 10235 | Zoll Cheswick, PA Assembler I HS diploma or equivalent Exp: 0-3 years |
The Assembler I’s primary function will be to perform light mechanical assembly and electronic assembly tasks as assigned. This includes the repair, assembly or disassembly of various devices. Essential Duties and Responsibilities: Works under direct supervision. Applies basic skills in procedures, techniques, tools, materials and equipment. Performs routine assembly, modification and repair of electronic and electrical assemblies. Working from noncomplex wiring and assembly drawings, operation sheets, engineering specifications, sketches and running sheets, performs initial and basic wiring and assembly operations to complete prototype and production units. Completes wiring connections from one terminal point to another and solders each terminal, working to close tolerances. Uses judgment in reworking or rewiring any unit to bring it within quality control specifications. etc. | 8/26/2020 |
| 10236 | Zoll Cheswick, PA Material Handler I HS diploma or equivalent Exp: 0-1 year(s) |
Performs manual and clerical duties related to shipping, receiving, inspecting, storing, issuing and delivering a variety of materials, equipment and supplies. Essential Duties and Responsibilities: Customer oriented. Perform Cycle Count daily. Process incoming Purchase Order receipts. Issue components to all types of work orders. Fill stock requests. Enter WIP receipts. Perform T-Transaction for quick turn items. Perform work order traceability. Locate raw material in bin location. Perform daily shipping activities. etc. | 8/26/2020 |
| 10237 | Zoll Pawtucket, RI QA Engineer BS/BA Exp: 1-3 year(s) |
The primary purpose of the position will be ensuring that complaints are properly investigated and documented as well as verifying that outgoing units comply with stated guidelines. In addition, the position supports the resolution of customer issues in order to determine the cause of the problem and to initiate the appropriate corrective action. In some cases, formal reports to customer will be required to explain the problem and what was done to correct it. Moreover, the Quality Assurance Engineer will be required to conduct analysis and trending of information and perform inspections on incoming finished goods. etc. | 8/26/2020 |
| 10238 | Zoll Chelmsford, MA Quality Assurance Engineer BS/BA Exp: 1-3 year(s) |
The primary purpose of the position will be ensuring that complaints are properly investigated and documented as well as verifying that outgoing units comply with stated guidelines. In addition, the position supports the resolution of customer issues in order to determine the cause of the problem and to initiate the appropriate corrective action. In some cases, formal reports to customer will be required to explain the problem and what was done to correct it. Moreover, the Quality Assurance Engineer will be required to conduct analysis and trending of information and perform inspections on incoming finished goods. etc. | 8/26/2020 |
| 10239 | Zoll East Providence, RI R&D Technician II AS/AA Exp: 0 years |
Perform R&D lab technician duties that include testing equipment, building prototype assemblies, building test equipment, and performing associated administrative duties such as lab cleanup and maintenance. Requires only moderate oversight in completing tasks. Essential Functions: Builds R&D test fixtures per specifications provided, providing design assistance and feedback. With minimal supervision, executes test protocols to completion, which includes coordinating the manufacturing and testing of the samples, reviewing the test procedures and data for accuracy and completeness, summarizing and analyzing the data or reviewing summaries for completeness, and informing the appropriate project leader of any questions or unexpected results that arise during testing. etc. | 8/26/2020 |
| 10240 | Solique Warsaw, IN Field Service Technician I AS/BS in electronics or industrial mechanics Exp: Not necessary for AS/BS candidates |
We are seeking a Field Service Technician to learn, develop and execute the basic necessary skills required to perform the job of a ZEISS Service Technician. Service Technicians install, troubleshoot and repair ZEISS Industrial Quality Solutions equipment onsite at our Customers Locations. We are looking for people who are keen to try something new: Demonstrate customer service skills and knowledge with a high level of passion and dedication. Demonstrate strong and efficient ability to learn a skill on entry class Coordinate Measuring Machines utilizing mechanical and electronic aptitude. etc. | 8/26/2020 |
| 10241 | Solique St. Cloud, MN Optical Lab Operator (Freeform, 1st Shift) HS diploma or equivalent Exp: 0-2 years |
Performs routine production duties associated with various aspects of lens production paying close attention to quality, quantity and efficiency. This position focuses on our Freeform Surfacing area washing lenses, inspecting and taping lenses, matching tools, polishing, running generators, inspecting and coating (backside). Qualifies and inspects product to ensure compliance with CZV specifications and standards. Complies with all safety regulations as well as maintains a clean and safe work environment. etc. | 8/26/2020 |
| 10242 | Solique St. Cloud, MN Optical Lab Operator (Distribution, 3rd Shift | 20% Shift Differential) HS diploma or equivalent Exp: 0-2 years |
Performs routine production duties associated with various aspects of lens production paying close attention to quality, quantity and efficiency. This position focuses on our Freeform Surfacing area washing lenses, inspecting and taping lenses, matching tools, polishing, running generators, inspecting and coating (backside). Qualifies and inspects product to ensure compliance with CZV specifications and standards. Complies with all safety regulations as well as maintains a clean and safe work environment. etc. | 8/26/2020 |
| 10243 | Solique St. Cloud, MN Optical Lab Operator (Presurfacing, 3rd Shift | 20% Shift Differential) HS diploma or equivalent Exp: 0-2 years |
Performs routine production duties associated with various aspects of lens production paying close attention to quality, quantity and efficiency. This position focuses on our Presurfacing area pulling lenses, training orders, tracing frames and pairing frames with orders. Qualifies and inspects product to ensure compliance with CZV specifications and standards. Complies with all safety regulations as well as maintains a clean and safe work environment. etc. | 8/26/2020 |
| 10244 | Solique Minneapolis, MN Field Service Technician I AS/BS in electronics or industrial mechanics Exp: Not necessary for AS/BS candidates |
Demonstrate customer service skills and knowledge with a high level of passion and dedication. Demonstrate strong and efficient ability to learn a skill on entry class Coordinate Measuring Machines utilizing mechanical and electronic aptitude. Perform necessary administrative paperwork in complete and accurate manner. Solutions oriented with ability to work independently in a high pressure, fast paced and innovative environment. Travel requirement is 80-100% including international as needed. etc. | 8/26/2020 |
| 10245 | CRISPR Therapeutics Cambridge, MA Research Associate (Toxicology) BA/BS Exp: 0-2 years |
CRISPR Therapeutics is seeking a motivated individual to join our in vivo pharmacology team. The candidate will be responsible for implementation of in vivo studies involving mice and rats and should be comfortable handling and administering test articles to both species. The team interacts with most of the research groups within CRISPR, offering the candidate exposure to a variety of different programs and platforms. The candidate will work with team members on all aspects of the in vivo study: design, administration, in-life observations, post mortem analysis, report generation, and data presentation. Familiarity with downstream analysis (necropsy, tissue collection, fixation, IF, IHC, ELISA, PCR) as well as cell culture is beneficial but not necessary. etc. | 8/26/2020 |
| 10246 | CRISPR Therapeutics Cambridge, MA Research Associate II/Sr. Research Associate, Analytical Development MS Exp: 1+ year(s) |
We are seeking a Research Associate to join an exciting, fast-growing and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. etc. | 8/26/2020 |
| 10247 | CRISPR Therapeutics Cambridge, MA Research Associate II/Senior Research Associate, Analytical Development (PCR/Genomics) MS Exp: 1+ year(s) |
We are seeking a Senior/Principal Research Associate to join an exciting, fast growing and well financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop and qualify PCR-based assays (qPCR and ddPCR) to measure gene editing in target and non-target cells, characterizing genome changes, as well as assays to measure viral genome titer. He or she will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and support process development and product characterization under guidance. etc. | 8/26/2020 |
| 10248 | CRISPR Therapeutics Cambridge, MA Research Associate II/Senior Research Associate (Cell Based Assays) MS Exp: 1+ year(s) |
We are seeking a Research Associate II/Senior Research Associate to join an exciting, fast-growing, and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. He or she will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. | 8/26/2020 |
| 10249 | CRISPR Therapeutics Cambridge, MA Research Associate II, Analytical Development MS Exp: 1+ year(s) |
We are seeking a highly organized Research Associate II to join an exciting, fast-growing and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, with a multi-functional skill set, such as developing and managing primary cell banks, execution of assays, as well as building a sample management system. The sample management aspect will be concentrated on the use of databases, such as Microsoft Access, Excel, and SharePoint and aid in organizing and keeping track of samples and internal distributions, where there is opportunity for movement. The cell banking aspect will focus on generating cell banks by isolating and characterizing primary cells from donor samples, complete donor screening, and work independently to support process development and product characterization. etc. | 8/26/2020 |
| 10250 | CRISPR Therapeutics Cambridge, MA Research Associate II, Analytical Development MS in a biological science Exp: 1+ year(s) |
We are seeking a Research Associate II to join an exciting, fast-growing, and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work to support process development, product characterization, and technical transfer to CMOs and GMP test labs. etc. | 8/26/2020 |
| 10251 | Casma Therapeutics Cambridge, MA Research Associate, Biology MS in biology or related Exp: 1-3 year(s) |
We are seeking a highly motivated, Research Associate to participate in drug discovery programs that lead to the identification of new targets and drug candidates for clinical development. The individual should possess strong core competencies in cell biology, molecular biology, assay development. We are seeking a qualified candidate who will share our excitement about the science, contribute to our culture, and honor our commitment to patients. Responsibilities: Cell culture and cell line development using retro- and lenti-virus, CRISPR and downstream analysis of autophagy and signaling. Perform western blotting, FACS and imaging analysis to analyze autophagy and specific target activity in primary cells and cell lines. etc. | 8/26/2020 |
| 10252 | BioLegend San Diego, CA Manufacturing Associate - Recombinant Protein Purification BS in a life science Exp: 1+ year(s) |
This position is responsible for manufacturing cutting edge recombinant protein research products in Molecular Cellular Immunology (MCI) manufacturing group. The Recombinant Manufacturing Associate will focus on recombinant protein purification. The duties include preparing buffer solutions, and purifying recombinant proteins to standard operating procedures. Another part of the job responsibility includes transferring the products to other groups, preparing product/project related documentation, and maintaining the production record for recombinant protein products. etc. | 8/18/2020 |
| 10253 | BioLegend San Diego, CA Bottling Technician - Formulation Group (1st shift 8:00am - 4:30pm) HS diploma or equivalent Exp: 6-12 months |
BioLegend is looking for a Bottling Process Technician for our Formulation Group. This role will be responsible for processing product formulations, filling, capping, labeling, and completing batch records, and putting away Finished Good Inventory (FGI). This is a highly team oriented group which involves working closely with other core teams within the Bottling Department as well as other departments such as Planning, Receiving, Inventory Control, Custom Solution Team (CST), Packaging and Quality Control groups. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Assist in performing various bottling related tasks to include dispensing antibody solutions and capping and labeling of vials, tubes or bottles. etc. | 8/18/2020 |
| 10254 | BioLegend San Diego, CA Packaging Technician HS diploma Exp: 6 months |
BioLegend is looking for an energetic Packaging Technician to work in our dynamic, fast paced warehouse environment. This position will entail picking a high volume of products based on orders processed and preparing them for shipment. This role involves a high degree of repetitive tasks with a focus on quality. Essential Functions: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Picking vials for orders processed according to the pick ticket for each order, triple-checking the order for accuracy, preparing for shipping. Ensuring correct products are picked and processed. etc. | 8/18/2020 |
| 10255 | BioLegend San Diego, CA Research Associate - Cell Analysis & Flow Cytometry BS/MS in a life science Exp: 1+ year(s) |
As a Research Associate, you will report to a Senior Scientist or Manager, where you will be able to conduct extensive analysis on new or existing products and consistently report key findings on product research initiatives. Under general supervision and with on-going review, this position researches, designs, develops and/or supports experiments for product development, process optimization applications, analytical methods, and validation activities ensuring a successful transition into a GMP manufacturing environment. The work requires routinely handling small animals and biological samples from animals and human donors. Prior experience in tissue culture, flow cytometry, immunoassays (eg ELISA, immunefluorescent/immune-histochemical staining, Western Blotting,), molecular biology techniques (eg PCR, cloning, etc.), data analysis, and project management are preferred. etc. | 8/18/2020 |
| 10256 | BioLegend San Diego, CA Manufacturing Associate - Conjugation (2nd Shift 4:00pm - 12:30am) AS in biochemistry, chemistry, or related Exp: 1 year |
The Manufacturing Associate will be an integral member of a team that ensures the highest quality of our finalized antibody products. This position offers the opportunity to gain experience with different types of conjugation chemistries and different chromatography methods to purify antibodies and offers the opportunity to work in small scale to large scale product projects and to learn to utilize the (Enterprise Resource Planning) ERP database to track production schedules and deadlines and to enter production results. This position will also perform scale ups and perform troubleshooting of problematic products, including continuous improvement methodologies for efficiency. etc. | 8/18/2020 |
| 10257 | BioLegend San Diego, CA Manufacturing Associate I - Purification (2nd Shift) BS in biology, biochemistry, chemistry, or other science Exp: 1+ year(s) |
The Manufacturing Associate position will function as an important member of the team that manufactures and provides antibodies and reagents to a diverse set of research areas including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology. This is a great opportunity for you to enhance your knowledge in the biotechnology industry. Essential tasks for this position include: following Standard Operating Procedures (SOP)s, creating and updating batch records, performing limited buffer preparation, cleaning glassware and restocking lab supplies. Additional responsibilities may also include processing troubleshooting and aliquoting bulk antibodies for finished goods inventory. etc. | 8/18/2020 |
| 10258 | BioLegend San Diego, CA Manufacturing Associate I - Conjugation (Brilliant Violet Group) AS in biochemistry, chemistry, or related Exp: 1 year |
The Manufacturing Associate position for BioLegend’s Brilliant Violet (BV) Conjugation Group will be responsible for performing all essential functions related to antibody conjugation, including following SOPs and batch records and maintaining and analyzing lot histories. This individual will be an integral member of specialized team that ensures the highest quality of our highly successful BV antibody products, and will offer the opportunity to gain experience with different types of conjugation chemistries. Due to the light sensitive nature of these products, Associates will work in facilities with red lighting to ensure product quality. Associates will also learn different chromatography methods to purify antibodies, and have the opportunity to work in small scale to large scale product projects while learning to utilize the Enterprise Resource Planning (ERP) database to track production schedules and deadlines and to enter production results. etc. | 8/18/2020 |
| 10259 | bioMerieux Lombard, IL Filling Operator I - Lombard, IL 1 HS diploma or equivalent Exp: 1 year |
As a Filing Operator 1, you will ensure goals are met through the understanding of objectives, communication with co-workers and supervisors, working safely, executing procedures, and ensuring the quality product is being manufactured. Employees are expected to stand for prolonged periods, perform basic mathematical equations, adhere to all verbal and posted guidelines, and be able lift up to 33lbs. Main Accountabilities: Perform packaging activities including but not limited to: label generation, visual inspection, heat sealing, and utilizing packaging equipment. Perform Filling activities in non-controlled areas: tube and bottle manufacturing. Perform routine cleaning tasks in relation to the manufacturing areas. Routinely checking inventory supplies and ensuring all levels are adequate. etc. | 8/18/2020 |
| 10260 | bioMerieux Murray, UT Software Test Engineer I AS/BS in engineering, computer science, or equivalent Exp: 0-3 years |
The software test engineer works aside the software team to assist in producing quality software. This position is responsible for the design, implementation and execution of tests to verify that software and firmware operate correctly and meet design specifications. This individual should work creatively to automate testing where feasible. This individual should have knowledge of one or more programming languages. This engineer is expected to work and communicate well with other members, team leadership as well as company management in order to meet the goals of the project. Principal Job Duties and Responsibilities: Perform all work in compliance with company policy and within the guidelines of the bioMérieux Quality System. If in a leadership role – is responsible for leading and managing the portions of the project to which he/she is assigned as a leader to accomplish the goals of the project. etc. | 8/18/2020 |
| 10261 | Bio-Rad Irvine, CA Tech Sup Rep I BS/AS Exp: 1-2 year(s) |
Responsible for providing technical support via phone and e-mail to external and internal customers, product support, R&D, marketing and sales group, selling units, distributors and other manufacturers for all QSD products. Includes familiarity with all QSD products, manage and analyze data, work with Customer Contact Report database, Unity/QCNet, and all other supporting programs. etc. | 8/18/2020 |
| 10262 | Bio-Rad Irvine, CA R&D Technical Associate HS diploma or equivalent Exp: 0-2 year(s) |
Bio-Rad is looking for a Technical Associate to work in the R&D Development group. The position requires a limited working knowledge of laboratory experimentation, general chemistry, and clinical chemistry. This position will assist and support the development of clinical chemistry controls. The ideal candidate will also possess abilities in data entry/input, and is comfortable working with blood, serum, urine and/or their various components. Responsibilities: Support product development activities through execution of simple routine laboratory tasks. etc. | 8/18/2020 |
| 10263 | Bio-Rad Irvine, CA Field Service Engineer AS/BS in electronics or related Exp: 0-2 year(s) |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers based in the Washington DC area traveling 50 – 75%. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. Act as customer advocate to ensure satisfaction and repeat business. Maintains company assets including parts inventory and leased vehicle. etc. | 8/18/2020 |
| 10264 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technician or Technologist, Hepatitis BS in medical technology, chemistry, biology or related Exp: 1 year |
The Medical Laboratory Technician will perform all necessary laboratory testing in the detection, diagnosis, and prognosis of disease. The Medical Laboratory Technician will work collaboratively with the laboratory team to provide testing services to the clients. Additional tasks can be assigned at the discretion of the Supervisor/Manager/Director. Duties may include but are not necessarily limited to the following: Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. etc. | 8/18/2020 |
| 10265 | BioReference Laboratories Columbus, OH TEMP Medical Lab Technician or Technologist BS in medical technology, chemistry, biology or related Exp: 1 year |
The Medical Laboratory Technician will perform all necessary laboratory testing in the detection, diagnosis, and prognosis of disease. The Medical Laboratory Technician will work collaboratively with the laboratory team to provide testing services to the clients. Additional tasks can be assigned at the discretion of the Supervisor/Manager/Director. Duties may include but are not necessarily limited to the following: Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. etc. | 8/18/2020 |
| 10266 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technician or Technologist, Microbiology (FT, 40 Hours) BS in medical technology, chemistry, biology or related Exp: 1+ year(s) |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Duties may include but are not necessarily limited to the following: Maintain standards in routine & STAT testing. Complete work in a timely manner. Write legibly when documenting QC, problems or information. etc. | 8/18/2020 |
| 10267 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technician or Technologist, Overnight (FT, 40hrs per week) BS in medical technology, chemistry, biology or related Exp: 1+ year(s) |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Duties may include but are not necessarily limited to the following: Maintain standards in routine & STAT testing. Complete work in a timely manner. Write legibly when documenting QC, problems or information. etc. | 8/18/2020 |
| 10268 | LGC Novato, CA GMP Manufacturing Tech 1- Weekend 3x12 Fri-Sun BS/BA Exp: Not necessary for bachelor's candidates |
The GMP Manufacturing Technician I position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. To perform this job successfully, an individual must be able to perform each essential function satisfactorily. Essential Functions: Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director. Maintain batch records, equipment logs and other production records as directed per company procedures. Maintain a clean an orderly laboratory environment. etc. | 8/18/2020 |
| 10269 | LGC Novato, CA GMP Manufacturing Technician I BS/BA Exp: Not necessary for bachelor's candidates |
The GMP Manufacturing Technician I performs tasks associated with the production of modified oligonucleotides in a high throughput time sensitive manufacturing environment. A GMP Manufacturing Technician I may be called upon to work in any production shift in the GMP Manufacturing Department. Areas of Responsibility: Performs all assigned job functions per documented procedures as directed by Supervisor. Performs daily equipment and lab maintenance tasks. Able to follow all documented procedures. Other duties as assigned. etc. | 8/18/2020 |
| 10270 | LGC Petaluma, CA Production Technician I, Oligo Liquid Handling BS in chemistry or life science Exp: 0-1+ year(s) |
A Production Technician I, Oligo Liquid Handling is responsible for performing day to day production activities in the custom oligonucleotide (oligo) Liquid Handling lab. Production activities will be performed in a timely fashion and in compliance with company procedures. The Liquid Handling team is responsible for ensuring oligos meet all customer specifications, and final processing prior to delivery to the customer. Areas of Responsibility: Performs all assigned job functions per documented procedures as directed by supervisor. Processes oligo samples in a high throughput production environment using automated Tecan liquid handlers. etc. | 8/18/2020 |
| 10271 | Bioserv San Diego, CA Manufacturing Technician I/II HS diploma or equivalent Exp: 1-2 year(s) |
The Manufacturing Technician is responsible for supporting and performing routine procedures associated with the manufacture of the customer’s product with minimal direction from Supervisor. Manufacturing Technicians responsibilities include performing environmental monitoring, cleaning and sterilizing of glassware, cleaning of clean-room suites, manufacturing preparatory activities and clean-up, assist in formulation, visual inspections, labeling and packaging. They may be aseptically qualified to perform aseptic manufacturing set-up, filtration, filling and closure of product. With sufficient Bioserv training, they may be a primary operator of complex equipment and processes, and additional tasks that are assigned by Management in compliance with QSR’s, SOP’s, and written procedures with direction from the Project Coordinator and/or Supervisor. etc. | 8/18/2020 |
| 10272 | Bioserv San Diego, CA Manufacturing Technician I HS diploma or equivalent Exp: 1-2 year(s) |
Under direct supervision, the Manufacturing Technician I will be responsible for supporting and performing routine procedures associated with the manufacture of the customer’s product. This individual will work independently once they are trained and experienced with technician tasks. Essential Duties & Responsibilities: Perform environmental monitoring and complete documents associated with the activity. Clean and sterilize glassware and other materials. Perform cleaning of cleanroom suites. etc. | 8/18/2020 |
| 10273 | Bioventus Tampa, FL Associate Sales Rep - Biomedical - Tampa, FL BS/BA in sports medicine, life science or a commercial discipline Exp: 0-2+ year(s) |
The Associate Sales Representative (ASR) is an entry level sales role at Bioventus. The ASR is primarily responsible for consulting with and providing clinical and technical information to healthcare professionals and their staff to achieve the sales objectives. Associate Sales Representatives will operate within company policies and procedures and demonstrate a high degree of compliant and ethical behaviors. Successful candidates should be open to relocation, at least to bordering states. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. etc. | 8/18/2020 |
| 10274 | Bioventus Stamford, CT Associate Sales Rep - Biomedical - Stamford, CT BS/BA in sports medicine, life science or a commercial discipline Exp: 0-2+ year(s) |
The Associate Sales Representative (ASR) is an entry level sales role at Bioventus. The ASR is primarily responsible for consulting with and providing clinical and technical information to healthcare professionals and their staff to achieve the sales objectives. Associate Sales Representatives will operate within company policies and procedures and demonstrate a high degree of compliant and ethical behaviors. Successful candidates should be open to relocation, at least to bordering states. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. etc. | 8/18/2020 |
| 10275 | Blueprint Genetics Seattle, WA Medical Technologist BS in a biological, chemical, or physical science Exp: 1 year |
The Medical Technologist performs tests requiring the exercise of independent judgment and responsibility in those specialties in which the Technologist is qualified by education, training and experience. In addition, the Medical Technologist is responsible for assuring that a given test system is operated in accordance with the laboratory's procedure manual and that the applicable quality control requirements are met. The incumbent actively supports and complies with all company and departmental policies and procedures. etc. | 8/18/2020 |
| 10276 | BlueRock Therapeutics Cambridge, MA Research Associate I/II, Genome Sciences BA Exp: 0-5 years |
We are seeking a research associate to join our newly formed Genome Sciences team in Cambridge. Reporting to the Scientist, she or he will play a central role in the development, production, and evaluation of CRISPR gene editing components for use in pluripotent stem cells. The qualified candidate will have solid experience in expression and purification of recombinant proteins from bacterial cell culture and have some proficiency with mammalian cell culture using aseptic technique. He or she will also be curious, innovative, persistent, and be able to work independently in the laboratory with minimal supervision. etc. | 8/18/2020 |
| 10277 | Boston Analytical Framingham, MA Environmental Monitoring Technician HS diploma/AA/AS Exp: None required |
The Environmental Monitoring Technician will perform Environmental Monitoring (EM) of pharmaceutical cleanrooms and the associated spaces on a daily basis according to FDA, cGMP and Boston Analytical’s/Client Standard Operating Procedures. Primary Duties and Responsibilities: Collects routine daily, weekly and monthly EM samples in pharmaceutical cleanrooms. Sample types include air viable, surface viable, and air nonviable monitoring. Collects compressed gas samples to ensure they are free of microbial and chemical contamination. Samples purified water system at both generation and point of use for subsequent analysis for Bioburden, TOC, Conductivity, and Endotoxin. etc. | 8/18/2020 |
| 10278 | Boston Analytical Salem, NH QA Specialist – All Levels BS in a scientific discipline Exp: 0-3 years |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing chemists analytical data, routine work, protocols and reports. Primary Duties and Responsibilities: Auditing chemists’ routine project folders for conformance to company and customer requirements. Write, review and edit Standard Operating Procedures (SOP’s, Forms and Methods) and familiarity with internal SOPs. Alternate contact person for QA questions relating to laboratory operations and client correspondences. Work with area management on the writing, issuance and tracking of deviations and investigations for closure. Perform and assist with GMP audits. etc. | 8/18/2020 |
| 10279 | Boston Analytical Salem, NH Scientist II – Method Development and Validation MS in chemistry or related Exp: 1+ year(s) |
The Scientist II conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. The position includes development of analytical methods and attendant procedures, as well as validation of analytical methods, including writing validation protocols and reports. Techniques will include analysis of pharmaceutical products using chromatographic techniques, spectrographic techniques, thermal analysis, and wet chemical analysis. Primary Duties and Responsibilities: Develops methods based on client requirements. Specific techniques include, but are not limited to HPLC, GC, AA, FTIR, and dissolution. Conducts research on manufactured products to develop, improve and validate test procedures. Validates methods compliant with regulatory requirements. etc. | 8/18/2020 |
| 10280 | Boston Analytical Salem, NH Microbiologist II BS in microbiology or related Exp: 1-5 year(s) |
The QC Microbiologist II conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. Primary Duties and Responsibilities: Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity). Performs genetic analysis of microbial growth to determine Genus/Species of unknown isolates. Collects Environmental Monitoring Samples onsite and offsite at client manufacturing sites. Documents work in a clear and organized manner. etc. | 8/18/2020 |
| 10281 | Boston Scientific Quincy, MA Inspector II - Incoming Inspection 1st shift Job HS diploma or equivalent Exp: 1-2 year(s) |
To perform inspection activities on products and to release products to Finished Goods or other release locations; control of products through such activities as inspection of new product lines to Finished Goods, processing shipping holds, processing/controlling pre-release product lines, processing scrap, processing quality records, processing Returns product inspection. Your responsibilities include: Perform inspection activities on products, in such categories as sterility inspection, incoming inspection, in process inspection and returns inspection. Complete data forms with the results of inspection activities, including non-conforming material reports, when required. SAP & WM transactions related to inspection activities. Insure completion of nonconforming reports and update the MRB system. etc. | 8/18/2020 |
| 10282 | Boston Scientific Arden Hills, MN Process Technician III Job AA/AS Exp: 1+ year(s) |
This position works independently to assist R&D and process engineers, scientists, and/or teams in the development and analysis of products, materials, processes, or equipment. Your Responsibilities Will Include: Participate in the operation and maintenance of process equipment. Develop concepts and accordingly construct prototypes/products from concepts. Explore and propose creative solutions based on solid rationales and contribute to design and process concepts. Organize, coordinate, and execute building and testing of prototypes/products per engineering instructions. etc. | 8/18/2020 |
| 10283 | Boston Scientific Maple Grove, MN Machine Operator I - 1st Shift - Maple Grove, MN--Extrusion Job AS/AA Exp: 1 year |
Primary focus is to build quality product by following processes to meet all production goals. Your Responsibilities Include: Understands and adheres to safety policies and practices. Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Gains basic understanding of Lean Manufacturing and related principles. Willing to flex and rotate as necessary and work well with all group members, both within the team and cross-functionally. etc. | 8/18/2020 |
| 10284 | Boston Scientific Maple Grove, MN Manufacturing Technician II (2nd Shift) Job AA/AS Exp: 0-3 years |
With general supervisory direction, assist in the daily support of products, processes, materials, and equipment in order to achieve production goals (i.e., quality, delivery, cost, productivity, and safety). Maintenance activities for automated PC and PLC controlled manufacturing equipment. Identify and troubleshoot process, material or equipment problems to minimize down time and improve process yields. Identify, design, and implement process equipment changes to improve reliability of the process. Modify existing and develop new tooling and fixtures. Revise existing documents, processes, and/or methods to correct or improve processes/product. Work with vendors/suppliers to procure and install tooling, fixtures, and/or equipment. etc. | 8/18/2020 |
| 10285 | Boston Scientific Maple Grove, MN Manufacturing Technician II (3rd Shift) Job AA/AS Exp: 0-3 years |
With general supervisory direction, assist in the daily support of products, processes, materials, and equipment in order to achieve production goals (i.e., quality, delivery, cost, productivity, and safety). Your Responsibilities Will Include: Maintenance activities for automated PC and PLC controlled manufacturing equipment. Identify and troubleshoot process, material or equipment problems to minimize down time and improve process yields. Identify, design, and implement process equipment changes to improve reliability of the process. Modify existing and develop new tooling and fixtures. Revise existing documents, processes, and/or methods to correct or improve processes/product. etc. | 8/18/2020 |
| 10286 | Boston Scientific Maple Grove, MN Manufacturing Engineer I Job BS in engineering Exp: 0-2 year(s) |
Your Responsibilities Will Include: Provides daily support of production, processes, materials and equipment in order to achieve NSM department goals (i.e. safety, quality, delivery, and cost). Works cooperatively with R&D, Process Development, Quality, Production, Regulatory, Equipment Engineering, Supply Chain, and Marketing to ensure project success. Successfully contributes to both new product development teams and product support, typically including the following activities: process capability studies, process development, Six Sigma and Value Improvement projects, report preparation and process/test documentation. Designs and coordinates standard engineering tests and experiments. Designs, procures, and fabricates equipment tooling and fixtures. etc. | 8/18/2020 |
| 10287 | Boston Scientific Quincy, MA Industrial Engineer I - Defined Term Job BS in industrial, mechanical, or manufacturing engineering Exp: 6+ months |
The Industrial Engineer is responsible for working with key business partners to drive value improvement guided by lean principles to support business strategy and priorities. The Industrial Engineer will also develop/implement continuous process improvement to ensure efficient and cost effective workflows/practices in a light manufacturing and distribution environment. Your responsibilities include: Assess process capabilities, prioritize process improvement opportunities, and innovate and implement process improvements on multiple and moderately complex processes. Coordinate and lead facility layout and design projects within business units. Coordinate and champion value improvement projects throughout the business. Conduct Lean training programs for employees at all leves and departments. Actively deploy and coach the organization on Lean and LBP Essentials. etc. | 8/18/2020 |
| 10288 | Bristol Myers Squibb Phoenix, AZ Operator I, Aseptic HS diploma or equivalent Exp: 1 year |
The Operator I is responsible for executing production activities required to successfully manufacture sterile injectable products. This is accomplished by ensuring equipment, materials, and other resources are in place to meet production demands. The Operator I demonstrates and assures production activities within manufacturing operations are executed following all GMP’s. In addition, work will be performed in complete accordance with all SOPs, Specifications, Batch Records, regulatory expectations, and company policies. This position will require overtime, shift work, and flexibility in scheduling of “set” shift hours at times, based on production demands or extraordinary circumstances. etc. | 8/18/2020 |
| 10289 | Bristol Myers Squibb Syracuse, NY Assistant Scientist BS in a biological science Exp: 0-3 years |
Duties/Responsibilities: Perform laboratory analysis of samples, using aseptic technique, following established procedures and in full compliance with official compendial, health authority regulations, and established BMS policies. Conduct qualification of methods and/or other laboratory studies, according to scientific protocols. Maintains accurate records of work performed and documents results, according to Good Documentation Practices and established procedures as well as perform data entry into LIMS, MODA and LES. Assist with review of worksheets and laboratory data as assigned. Assists in the investigation of OOS results in areas of assigned responsibility. Operates and maintains laboratory instruments, while ensuring the reliability of instrumentation through proper maintenance, with ability to troubleshoot minor issues. Must analyze, evaluate, and interpret data, notifying clients of results, and assisting to resolve issues, if applicable. etc. | 8/18/2020 |
| 10290 | Bristol Myers Squibb Syracuse, NY Dispensary Warehouse Technician I BS/BA Exp: 1+ year(s) |
The primary role of the Dispensary Warehouse Technician is to perform functions relevant to Warehouse, Dispensary, and staging activities in the manufacturing facility. Core functions include Receiving materials, Material Transfers, SAP functions for inventory control, dispensing, material returns, and raw material sampling. Related activities include supply upkeep, cleaning, and bulk chemical transfers. All operations are to be performed in a safe and compliant manner. Duties/Responsibilities: Accurate receipt and unpacking of all process related direct inventory materials, indirect supplies, miscellaneous equipment, and material transfers. Including wipe down processes, SAP transactions, and proper storage adherence. Material transfers and movements from location to location. etc. | 8/18/2020 |
| 10291 | Bristol Myers Squibb Summit, NJ Manufacturing Associate, CAR-T BS/BA Exp: Not necessary for bachelor's candidates |
Manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Duties and Responsibilities: Production of blood component lots through selection, activation, transduction, cell culture, harvest, and cryopreservation. Aseptic technique is required for most activities: tube welding, connections, and transfers, at minimum. Weighs and measures in-process materials to ensure proper quantities are added/removed. Adheres to the production schedule ensuring on-time, internal production logistics. etc. | 8/18/2020 |
| 10292 | Icon Raleigh, NC Associate Project Manager Translations BS/BA in languages/translations Exp: 1-3 years in translation |
As Translation Associate Project Manager you are responsible for the coordination, execution, control and completion of single service projects ensuring consistency with ICON SOPs, service-line best practices, project contracts and budgets. Lead the planning and implementation of single service projects. Define project tasks and resource requirements based on project plans | 8/16/2020 |
| 10293 | Icon Knoxville, TN CRA I BS/Ba Exp: 12 months as an independent monitor |
As a Clinical Research Associate I at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - III, ensuring adherence to applicable regulations and principles of ICH-GCP. | 8/16/2020 |
| 10294 | Icon Raleigh, NC Proposals Development Assoc II BS/BA in sciences or business Exp: 1-3 years within CRO, Pharma or Healthcare |
This particular role would support our Laboratory Services Division. As a Senior Proposals Development Associate you will support Business Development in the winning of new business for ICON Laboratory Services through delivery of high quality customer-focused proposals and budgets for the conduct of clinical trials in response to Requests for Proposals (RFPs). | 8/16/2020 |
| 10295 | Icon Wilmington, NC CRC Assistant BS/BA in sciences/healthcare Exp: 1-3 years |
Performs study start-up duties including the production of a recruitment tool, and progress notes, as well as phone screening patients and identifying participants for trials on site. Proactively develops and executes recruitment plans that meet and exceed enrollment goals. Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment. | 8/16/2020 |
| 10296 | Icon Raleigh, NC Clinical Research Associate II BS/BA in healthcare/sciences Exp: 12-18 months as independent monitor as CRA |
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. | 8/16/2020 |
| 10297 | ICU Medical Salt Lake City, UT Repair Technician - temp/entry level HS Diploma/GED or AS in technical discipline Exp: 0-2 years |
The Service Hub Technician is responsible for triaging devices where critical decisions are made on the PCI, repair, updating of service record, tracking labor and material as well as updating and printing of a Service Report that is returned with the repaired device. | 8/16/2020 |
| 10298 | ICU Medical Salt Lake City, UT Material Handler M-F 6-2:30 HS Diploma/GED Exp: 1 year in warehouse/material handling |
The Material Handler supports Production by moving, transferring and pulling orders needed to support Production. The Material Handler performs inventory transactions in Oracle and delivers products to production to complete work orders. Operate Forklift, Walkie Rider, Order selector or pallet jack as needed to provide materials to Production areas | 8/16/2020 |
| 10299 | ICU Medical Austin, TX Instrumentation & Calibration Technician Associates in sciences/technology/engineering Exp: 0-3 years in instrumentation/calibration |
Calibrate instruments and devices in the calibration and preventive maintenance program. Resolve complex repetitive instrument problems. Assist Calibration supervisor in determining preventive maintenance and calibration programs/maintenance procedures are followed. Trouble-shoot and repair instruments and systems. | 8/16/2020 |
| 10300 | IGM Biosciences Mountain View, CA Research Associate / Senior Research Associate, Biomarkers MS in relevant Exp: 1+ years in industry/academia |
Our Preclinical Sciences group is looking for a Research Associate with a background in Immunology, Cell Biology or a related scientific discipline to join our growing and friendly team during this exciting time in our expansion. Duties include: Human and mouse cell culture and primary cell maintenance and isolation. Design, develop and execute in vitro cell-based immunoassays. | 8/16/2020 |
| 10301 | iHear San Leandro, CA Audiologists/Hearing Care Professionals, Hearing Aid Startup Degree in audiology Exp: 1 year in hearing aid dispensing |
Working with research & development, sales, and customer support with issues related to product, inquiries, orders, fulfillment and post sales support. Help establish systems and procedures for professional support. Provide audiology or dispensing knowledge to the organization. Provide customers with support regarding product selection, programming of our proprietary hearing devices, web-applications, software installations, etc. | 8/16/2020 |
| 10302 | Illumina Foster City, CA Research Associate I Fluidic Systems BS or MS in chemical/bio engineering Exp: 1-2 years in R&D |
Conduct focused research and development under general direction of supervisor to plan, conduct, analyze, interpret, and report recommendations based on experimental results in routine setting. Develop new sequencing applications, assay workflows and assay automation methods. Plan controlled experiments to characterize key components and finished reagents | 8/16/2020 |
| 10303 | Illumina Foster City, CA Equipment Engineer I-II (1st Shift) Bs or MS in engineering/sciences Exp: 1-5 years in CxP lab |
The Equipment Engineer I-II will be responsible for integration, implementation, service and maintenance of laboratory equipment. This will include automation and instrumentation in support of a Clinical, Research and various GxP Laboratories.This includes installation, configuration and repair of equipment, integrating equipment with information systems and validation and verification of the equipment in accordance with CLIA, cGMP and/or GLP guidelines. | 8/16/2020 |
| 10304 | Illumina Foster City, CA Engineer 1 - Fluidic Systems MS in mechanical engineering, bioengineering, or physics Exp: 1-2 years in lab environment |
As an Engineer 1 in the Research and Technology Development department, you will support the development of novel microfluidic-based sequencing platforms. You will be part of a multidisciplinary team solving complex problems, investigating new research areas and working on integration challenges. | 8/16/2020 |
| 10305 | Illumina San Diego, CA Manufacturing Specialist 1 BS/BA in related Exp: 0-1 years |
Able to formulate All Scale reagents under detailed direction of Work Instruction and ensure production order meets QC functional testing requirements and acceptance criteria. Quality review and release of Manufacturing DHRs for Reagents and Consumables in CamStar; Facilitate and help the manufacturing team resolve batch record data discrepancies | 8/16/2020 |
| 10306 | Illumina San Diego, CA Research Associate 2 BS in engineering or sciences Exp: 1-2 years in wet lab experience |
As a Research Associate 2 at Illumina in Systems Integration, you will work in a dynamic, team-oriented environment and help create genomic analysis tools used in the leading edge of research to advance human health by unlocking the power of the genome. Hands-on testing and integration of systems - hardware, software, chemistry, and application components | 8/16/2020 |
| 10307 | Illumina Madison, WI Quality Ops Analyst BS/BA in sciences Exp: 0-3 years in FDA/ISO regulated industry |
This position is responsible for performing Quality Assurance activities and is accountable for ensuring compliance with established procedures and requirements. This individual is authorized and designated by Illumina to conduct quality inspections of product and associated documentation to ensure compliance with established procedures and requirements | 8/16/2020 |
| 10308 | Imarc Minnetonka, MN Clinical Research Associate BS/BA in science, engineering or RN Exp: 18 months in clinical research |
The primary focus of this position is on routine monitoring and management of the research-related activities at a clinical site. Once fully trained, a Clinical Research Associate will be expected to perform site initiation, periodic, and close-out visits. Additionally, the Clinical Research Associate will be expected to serve as a resource and research liaison between assigned sites and the Sponsoring companies or CROs. | 8/16/2020 |
| 10309 | Imarc Strongsville, OH Clinical Research Associate BS/BA in science, engineering or RN Exp: 18 months in clinical research |
The primary focus of this position is on routine monitoring and management of the research-related activities at a clinical site. Once fully trained, a Clinical Research Associate will be expected to perform site initiation, periodic, and close-out visits. Additionally, the Clinical Research Associate will be expected to serve as a resource and research liaison between assigned sites and the Sponsoring companies or CROs. | 8/16/2020 |
| 10310 | Immucor Norcross, GA Medical Laboratory Technologist Associates or BS/BA Exp: 6-12 months related experience |
As a Medical Technologist, you will perform all assigned tasks following applicable laboratory SOPs, OSHA regulations and cGMP regulations (i.e. blood borne pathogens and chemical hazards). You will assist the department supervisor and/or manager with investigations, root cause analyses, and reports of out-of-specification results and deviations. You will also be responsible for maintaining and compiling Device History Records. | 8/16/2020 |
| 10311 | Immucor Warren, NJ Manufacturing Associate Assocites Exp: 1 year in cGMP manufacturing |
As the Manufacturing Associate, you will perform setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency. Formulating custom bulk reagents - involves working with pipettes and balances | 8/16/2020 |
| 10312 | Immucor Norcross, GA Production Technician HS Diploma/GED or AS in technical discipline Exp: 0-2 years in clean room environment |
As a Production Technician, you will perform tasks and administrative aspects regarding packaging operations according to department procedures, specifications or work instructions. This includes starting up/breaking down operations, clearing operations areas, calculating component usage, verifying counts of products in and out of operations, and visual inspections of products for defects. | 8/16/2020 |
| 10313 | Immucor Norcross, GA Supply Chain Analyst BS/BA in engineering Exp: 1-3 years in related |
As a Supply Chain Analyst, you will use analytical and quantitative methods to understand, predict, and enhance supply chain processes by assembling data, analyzing performance, identifying problems, and developing recommendations to support SCM planning and manufacturing operations. | 8/16/2020 |
| 10314 | Immucor Warren, NJ Manufacturing Associate Associates degree Exp: 1 year in cGMP manufacturing |
As the Manufacturing Associate, you will perform setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency. Formulating custom bulk reagents - involves working with pipettes and balances | 8/16/2020 |
| 10315 | Immucor Norcross, GA Production Technician HS Diploma/GED or AS in technical discipline Exp: 0-2 years in clean room environment |
As a Production Technician, you will perform tasks and administrative aspects regarding packaging operations according to department procedures, specifications or work instructions. This includes starting up/breaking down operations, clearing operations areas, calculating component usage, verifying counts of products in and out of operations, and visual inspections of products for defects. | 8/16/2020 |
| 10316 | Immucor Waukesha, WI Production Chemist BS/BA in chemistry/life sciences Exp: 0-2 years working with automated filling equipment a plus |
As Production Chemist, you will be responsible for subassembly formulation, raw material preparation and/or processing, QC testing reagent or component formulation, and some in-process testing. You will manage the development, planning, and implementation of manufacturing methods, processes, and operations for new or existing products or technologies. | 8/16/2020 |
| 10317 | Immune technology Corp New York, NY Sales Associate BS/BA in life sceinces Exp: 1 year in sales/marketing |
Full/part time position, responsible for ensuring customer retention through account management and increasing revenue through marketing activities and generation of sales leads. Establishing and retaining customer relationships primarily through phone, e-mail and personal visit. Delivering requested documents, literature, and information to customers | 8/16/2020 |
| 10318 | Bayer Creve Coeur, MO Production Associate BS/BA Exp: 1+ year(s) |
The primary responsibilities of this role, Production Associate, are to: Embrace and demonstrate a safety-first culture at all times; Perform daily operations as directed by site leadership; Be accountable for safe and timely delivery of quality supply based on production schedules while maintaining an efficient operation; Perform duties in a manner that support overall site Key Metrics including Safety, Quality, TIP (total individual volume performance), TOP (total overall volume performance) and cost efficiency; etc. | 8/11/2020 |
| 10319 | Bayer Berkeley, CA Production Specialist III CCTC MS Exp: Not necessary for MS candidates |
The primary responsibilities of this role, Production Specialist III of Cell Culture Technology Center (CCTC), are to: Be responsible for all aspects of clinical manufacturing in the following areas such as Cell Expansion, Cell Culture, Purification, Solution Preparation and Weigh/Dispense and work seamlessly across all areas and will be an SME for NLT one area; Participate in new products introductions (NPIs) into CCTC with support from BD and MSAT; Ensure all activities are performed to schedule; Act as delegate to Senior Production specialist; Collaborate with BD and MSAT to ensure cross functional alignment with platform process, equipment, raw materials and/or automation for NLT one area; etc. | 8/11/2020 |
| 10320 | Bayer Jerseyville, IL Agronomic Research Specialist MS/MA Exp: 0-2 years |
The primary responsibilities of this role, Agronomic Research Specialist II, are to: Be responsible for the implementation of unique and innovative technology solutions designed to improve research design and operations success through the use of new tools and methodologies to improve overall plant breeding phenotyping such as the pilot and use of geospatial systems, agronomic planting and harvesting tools, harvesting shelling systems and data capture applications; Collaborate with project team members to deliver detailed experimental protocols that enable advancement decisions by our scientists and placement decisions to our customers; etc. | 8/11/2020 |
| 10321 | Bayer Kansas City, MO R&D Specialist II-Product Support MS in chemistry, biology, engineering or related Exp: Not necessary for MS candidates |
The primary responsibilities of this role, R&D Specialist II, are to: Provide development expertise for new formulations by providing Pilot Scale knowledge and advise and Startup assistance for production plants; Assist Product Supply and Supply chain by performing studies related to product quality and assurance of supply; Prioritize and can coordinate work within a large team; Provide training to third party reports; Maintain detailed record keeping and required documentation; Be accountable for cross-functional work within platform and/or across process areas; etc. | 8/11/2020 |
| 10322 | Bayer Saxonburg, PA Assembler I Day Shift 6am-6pm HS diploma or equivalent Exp: 1+ year(s) |
The primary responsibilities of this role, Assembler I, are to: Assemble various products; Package various products; Perform rework and inspection on the product; Back up higher-level positions; Have awareness of quality standards and ability to identify defects in products; Record data related to product quality and traceability; Clean of work areas as required; etc. | 8/11/2020 |
| 10323 | Bayer Kearney, NE Production Associate BS/BA Exp: 1+ year(s) |
The primary responsibilities of this role, Production Associate, are to: Embrace and demonstrate a safety-first culture at all times; Perform daily operations as directed by site leadership; Be accountable for safe and timely delivery of quality supply based on production schedules while maintaining an efficient operation; Perform duties in a manner that support overall site Key Metrics to include: Safety; Quality, TIP (total individual volume performance), TOP (total overall volume performance), and cost efficiency; Embrace an environment that promotes the building of good working relationships within the site; Participate in the execution of HSE, Quality Management System (QMS) and One PSS programs and elements; participates in associated networks; Contribute in plant operations such as conditioning, packaging, lab operations, warehouse / inventory management / distribution, carryover, etc., as assigned by the site leadership team; etc. | 8/11/2020 |
| 10324 | Bayer , OH Field Sales Rep I BS/BA Exp: 1+ year(s) |
As a Field Sales representative for Channel, you will be responsible for growing the market share of Seed & Trait business within Northwest Ohio covering the counties of Darke, Mercer, Van Wert, Paulding, Defiance, Henry Putnam, Allen, Auglaize, Shelby, Logan, Hardin, and Union. In this position, you will create demand for Bayer seed growth and Seed & Trait chemistry products through retailers, dealers, and top growers. The primary responsibilities of this role, Field Sales Representative I, are to: Develop and implement dealer business plans, manage forecasting, inventory management and product line demand issues, set the business direction, and coordinate follow-ups with dealers; Serve as the key business consultant to retailers and dealer and effectively sell the value of Bayer crop science products; etc. | 8/11/2020 |
| 10325 | Beckman Coulter Diagnostics Chaska, MN Scientist I Production Operations BS in biology, microbiology, or related Exp: 0-2 years |
Key Responsibilities: Read, comprehend and follow established work instructions and procedures with emphasis on quality. Execute the daily production plan to due date conformance and quality standards. Train to Standard Operating Procedures (SOPs). Follow engineering drawings, work order information, SOPs, and other written and verbal specifications in the manufacturing process while maintaining FDA requirements. Handle a variety of cell lines with a strict attention to detail while working aseptically. Independently execute work regarding maintenance of cell cultures, processing cellular material and releasing builds according to schedule. Apply basic analytical skills, critical thinking and scientific methods to perform daily tasks. Perform the set-up, calibration, testing and troubleshooting of instruments, such as large-scale bioreactor systems. Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements. etc. | 8/11/2020 |
| 10326 | Beckman Coulter Diagnostics Chicago, IL Field Service Engineer - Laboratory Instrumentation and Automation: Chicago AS/BS Exp: 1-3+ year(s) |
Beckman Coulter Diagnostics Field Service Engineers provide excellent customer service to clients while installing and maintaining diagnostic instrumentation and systems in hospital and stand-alone laboratory environments. As a Field Service Engineer (FSE) you will be the face of Beckman Coulter to customers and support them, directly impacting patient health and overall well-being. Would you like to be part of a team providing front line support to hospital laboratories? Are you ambitious and seeking to drive healthcare forward? The Field Service Engineer in this position will: Under minimal supervision, serve as lead to assigned customers; complete troubleshooting, installation, validation, maintenance, and service repair needs on designated equipment. May assist and/or train newer Field Engineers. Provide excellent and efficient service to Beckman Coulter’s customers, along with technical training on products. Repair, maintain, and install product line(s). etc. | 8/11/2020 |
| 10327 | Beckman Coulter Diagnostics Miami, FL Biomedical Customer Technical Support AS/BS in biology, biomedical engineering, electrical engineering, chemistry, or related Exp: 1-2 year(s) |
1st, 2nd or 3rd shift positions. Will require rotating weekends, holidays and to backfill vacation requests for other team members. Provide general technical consulting to customers and company staff distinguishing among hardware, reagent and software issues in order to resolve or dispatch the appropriate resource at minimum company expense. Associate will work in the Miami, Florida campus. Primary Duties and Responsibilities: Fielding Customer Calls to Facilitate 24/7 Support Function. Through telephone and electronic (i.e. email) technology provide resolutions on Hardware, Software, Assay and Training related calls from existing customer base. Measured on ability to work efficiently and resolve customer issues using the most cost effective solution. etc. | 8/11/2020 |
| 10328 | Beckman Coulter Diagnostics Louisville, KY Field Service Engineer-Louisville, KY AS/BS Exp: 1-3+ year(s) |
Beckman Coulter Diagnostics Field Service Engineers provide excellent customer service to clients while installing and maintaining diagnostic instrumentation and systems in hospital and stand-alone laboratory environments. As a Field Service Engineer (FSE) you will be the face of Beckman Coulter to customers and support them, directly impacting patient health and overall well-being. Would you like to be part of a team providing front line support to hospital laboratories? Are you ambitious and seeking to drive healthcare forward? The Field Service Engineer in this position will: Under minimal supervision, serve as lead to assigned customers; complete troubleshooting, installation, validation, maintenance, and service repair needs on designated equipment. May assist and/or train newer Field Engineers. Provide excellent and efficient service to Beckman Coulter’s customers, along with technical training on products. Repair, maintain, and install product line(s). etc. | 8/11/2020 |
| 10329 | Beckman Coulter Diagnostics Brea, CA Systems Engineer II MS in electrical, mechanical, biomedical, or related engineering Exp: 0-2 years |
We are looking for an engineer to be part of our Clinical Diagnostics Chemistry and Immunoassay Instrument R&D group in Brea, CA. This is an exciting product development opportunity where the primary responsibility will be to perform the following Systems Engineering functions. In this role, you will have the responsibility to: Collect appropriate data to define, identify, analyze, correct and prevent potential system failures. Develop test plans and conduct bench and system level testing that cover the expected customer use environment and operation conditions. Analyze and develop system and sub-system requirements and relationships with component specifications. Analyze, summarize, present, and interpret experimental data to formulate conclusions and make recommendations. etc. | 8/11/2020 |
| 10330 | Beckman Coulter Diagnostics West Sacramento, CA Customer Technical Specialist - Microbiology AS in microbiology or related Exp: 1-3 year(s) |
Primary Duties and Responsibilities: We are looking for an energetic, dynamic individual to join our team! The ideal candidate will thrive in a fast-paced, high-volume call center environment and whose passion includes the delivery of exceptional, results oriented experiences for our customers and the patients they serve. Handling Customer Calls to facilitate a 7-day Call Center Support Function. You will be expected to rotate holidays and assist in back filling vacation request for your peers. Provide technical resolutions on Hardware, Software, Consumables and LIS related calls from existing customer base through telephone and electronic (i.e. email, fax, remote diagnostics) technology. Possess excellent phone soft skills and communication skills, both verbal and written. Assign calls to field service when unable to resolve over the phone. etc. | 8/11/2020 |
| 10331 | Berg Health Framingham, MA Laboratory Operations Specialist I AS/BS Exp: 0-2 years |
Laboratory Operations Specialist I is a dynamic position that supports all lab operations within the OMICS and Bioanalytical Lab teams ensuring a safe work environment, by maintaining a clean, organized lab and facilitating training as necessary. The successful Lab Support Specialist prioritizes duties for continuous and measurable improvement in the lab. Laboratory Operations Specialist will work primarily in our labs and support instrument calibration, PM tracking, scheduling, and consumables inventory. etc. | 8/11/2020 |
| 10332 | BGI Montreal, QC Lab Technician BS in microbiology or related Exp: 1-2 year(s) |
The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. Major Responsibilities: Execute on and assist in the development of process instructions that ensure accuracy, throughput, and quality. Operate and monitor laboratory automation and instrumentation. Communicate issues and failures as necessary to the appropriate parties. Apply knowledge and experience in specialized areas, with an understanding of the underlying biochemistry. Use that knowledge and understanding to address problems and situations ordinarily encountered in laboratory manufacturing processes. etc. | 8/11/2020 |
| 10333 | Bicycle Therapeutics Lexington, MA Research Associate– Immuno-oncology BS/MS Exp: 1-5 year(s) |
The Research Associate, Immuno-oncology will be primarily responsible for the development and execution of essential in vitro and ex vivo assays of systemic and tumor-targeted immune cell agonists to enhance progress of Bicycle’s oncology pipeline. In this role, he or she will be a key player in implementing the in vitro characterization of our immune modulators. ey Responsibilities: The applicant will have a strong scientific background and hands-on laboratory skills in immunology, immuno-oncology and/or translational oncology with experience in immunological assay development and in vitro pharmacology. The successful candidate will work as part of a team and will be responsible for running and interpreting immunological and cell-based assays to characterize Bicycle® immune modulators. etc. | 8/11/2020 |
| 10334 | BillionToOne West Menlo Park, CA Laboratory Technician BS in biology or related Exp: 6+ months |
The CLA I is responsible for assisting with the day-to-day operations and equipment maintenance in the Clinical Laboratory. The CLA I will also be responsible for the pre-analytical phase of testing (e.g., specimen receipt, accessioning, and plasma/buffy coat isolation), performing quality assurance procedures, and complying with all local, state, and federal laboratory requirements. Responsibilities: Perform sample accessioning and isolation procedures according to the laboratory’s standard operating procedures; Clean labware, equipment, and benches; Prepare documents for equipment and personnel records; etc. | 8/11/2020 |
| 10335 | BillionToOne West Menlo Park, CA Research Associate BS/MS in microbiology, bioengineering, bioinformatics, physics or related Exp: 1-2 year(s) |
Key Responsibilities: Develop sophisticated and robust next-generation sequencing analysis pipelines under the guidance of a Senior Scientist. Work closely with Process Engineers to design process improvement experiments and analyze the resulting data. Perform analysis of clinical bioinformatics data. Assemble and analyze quality metrics from the clinical laboratory. Collaborate with Senior / Principal Scientists and support new scientific insights. etc. | 8/11/2020 |
| 10336 | BioAgilytix Durham, NC Business Development Assistant (temporary) BS in biological science, business administration or related Exp: 1+ year(s) |
Essential Responsibilities: Schedules initial teleconferences with relevant prospects for the Business Development team through cold calling and personalized email messaging; uses established contact lists, email templates, and call scripts to send 300+ emails and make 200+ calls per week. Tracks all activities and ensures meetings scheduled are properly inputted into CRM system (Salesforce). Performs administrative support work specific to sales and marketing departments. Other duties as needed. etc. | 8/11/2020 |
| 10337 | BioAgilytix Durham, NC Analyst, Business Development BS/BA in business administration, finance, marketing or related Exp: 0-2 years |
The Business Development Analyst will identify, analyze, and interpret trends in complex data sets and complete internal reporting on key sales metrics. He or she will present insights and recommendations in a consultative manner to internal stakeholders. Essential Responsibilities: Maintains schedules and completes routine internal reporting on key sales metrics. Prepares and provides supporting analysis for month-end, quarter-end, and year-end reporting and metrics. Generates sales performance dashboards and reports using SalesForce. etc. | 8/11/2020 |
| 10338 | BioAgilytix Boston, MA Analyst BS/MS in molecular biology, biochemistry, immunology or related Exp: 1 year |
Essential Responsibilities: Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export). Prepare summary tables. Peer review raw data. Order reagents. Participate in assay development and validation. Run assays independently. Adhere to provided method/directive. Prepare buffers. Use LIMS system. Participate in sample analysis. Pipetting. etc. | 8/11/2020 |
| 10339 | BioAgilytix Durham, NC Analyst BS/MS in molecular biology, biochemistry, immunology or related Exp: 1 year |
Essential Responsibilities: Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export). Prepare summary tables. Peer review raw data. Order reagents. Participate in assay development and validation. Run assays independently. Adhere to provided method/directive. Prepare buffers. Use LIMS system. Participate in sample analysis. Pipetting. etc. | 8/11/2020 |
| 10340 | BioAssay Systems Hayward, CA Research Associate - Manufacturing BS in chemistry, biochemistry or biology Exp: 1-2 year(s) |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing, and packaging the finished products. This candidate may also join part time in our R&D team. etc. | 8/11/2020 |
| 10341 | BioAssay Systems Hayward, CA Research Associate - Assay Development BS in chemistry, biochemistry or biology Exp: 1-2 year(s) |
We currently have an exciting opportunity for an enthusiastic research associate to join our growing R&D team. This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers. etc. | 8/11/2020 |
| 10342 | Biocare Medical Pacheco, CA Associate I, Product Development BS in biology or related Exp: 0-3 years |
The Associate I, Product Development functions with minimal supervision and guidance within the Reagent Research and Development Laboratory. The Associate I conducts product development activities on new and existing products involving Immunohistochemistry (IHC) and in situ hybridization (ISH) procedures within well-defined guidelines. The Associate I keeps abreast of current methodologies and developments within defined areas of research. The Associate I will at times assist other laboratory members or technical staff on research-related activities. etc. | 8/11/2020 |
| 10343 | Biocare Medical Pacheco, CA Associate I, Optimization Experience BS/AS in biology or related Exp: 0-5 years |
The Optimization Experience Associate functions with minimal supervision and guidance within the research and development (R&D) laboratory. The Optimization Experience Associate will conduct various R&D activities on new and existing products involving immunohistochemistry (IHC) procedures including, but not limited to, new product designs and optimizations. The Optimization Experience Associate will assist with troubleshooting of reagents and IHC staining, optimization of client menus and any pre-installation tasks needed to ensure client satisfaction. The Optimization Experience Associate is responsible for collecting and organizing relevant data to be used in the distribution to the applicable teams. etc. | 8/11/2020 |
| 10344 | Biocare Medical Pacheco, CA Associate Scientist I, Product Development MS Exp: 1-3 year(s) |
The Associate Scientist I, Product Development functions with minimal supervision and guidance within the Reagent Research and Development Laboratory. The Associate Scientist I conducts R&D activities on new and existing products involving Histology and Immunohistochemistry (IHC) procedures within well-defined guidelines. The Associate Scientist I keeps abreast of current methodologies and developments within defined areas of research. The Associate Scientist I participates in research or clinical collaborative projects. The Associate Scientist I will at times assist other laboratory members or technical staff on research-related activities. etc. | 8/11/2020 |
| 10345 | Biocare Medical Pacheco, CA Associate I, Product Design BS Exp: 0-3 years |
Assists the activities associated with IVD reagent development under Design Controls. Supports documentation of new product development and sustainability of existing products to ensure accurate and complete Design records. Contributes to the overall Quality Systems compliance of the Reagent R&D group. Essential Duties and Responsibilities: 1. Product Development/Design Control: a. Facilitates product development projects. b. Drafts Design Outputs for review by Manager, Product Design. etc. | 8/11/2020 |
| 10346 | Biocare Medical Pacheco, CA Laboratory Assistant BS in a scientific or engineering field Exp: 0-2 years |
Assist with product development testing tasks and manage assigned lab duties. Essential Duties and Responsibilities: Perform general laboratory related job duties as required. Maintain laboratory equipment logs, stocks solutions and lab supplies. Review and execute test protocols for integration test plan of new and sustaining engineering projects. Enter and update defects in defect management database. Assist with assigned testing and documenting results. Follow all company policies and procedures to ensure product integrity and quality control. Maintains good communication within the team and with other groups involved in the project. etc. | 8/11/2020 |
| 10347 | Bioclinica Princeton, NJ Auditor I, Medical Imaging AS in a life science, trial or quality maintenance, or computer science Exp: 0-3 years |
Supports all aspects of audits / audit conduct. Plans, conducts, and reports audits according to Bioclinica’s standard operating procedures (SOPs) and electronic document management system (EDMS) processes. Tracks and/or trends audit issues and/or CAPAs until closure. Provides root cause guidance to CAPA owners and/or conducts root cause analysis when assigned. Champions timely management of quality event reports, audit findings, and CAPAs. Follows-up and verifies effectiveness checks. Ability to work with all levels of Bioclinica personnel and external personnel in a professional and organized manner. Identifies and implements process improvements, with a focus on the audit program. Supports all audit/inspection types (e.g. internal, external, vendor, regulatory inspections, registrar {ISO, SOC etc.}) etc. | 8/11/2020 |
| 10348 | Bioclinica Princeton, NJ Associate Medical Writer BS in a life or physical science Exp: 1-2+ year(s) |
Performs study start up responsibilities by: Performing new award tasks such as entering new studies into the MedComm database, creating Medical Affairs and Medical Communications study-specific folders, organizing study documents, requesting signed Protocols, entering document costs in the new award spreadsheet, and notifying assigned Project Teams. Performing a concise and thorough review of study Protocols related to imaging requirements, schedules and windows. Creating, modifying and finalizing Site Manuals, associated fillable forms, and labels. Creating, modifying and finalizing Study Start-Up related Compliance Reports (CRs) such as Protocol Amendment Impact Forms (PAIFs), Notes to File (NTFs), Corrections, non-Quality Event Deviation Reports, and Transfers of Obligation (ToO) as required/applicable. etc. | 8/11/2020 |
| 10349 | Bioclinica Princeton, NJ Inside Sales Associate BS/BA Exp: 1-3 year(s) |
Support business development efforts. Contact clients directly at an early stage of the sales lifecycle to initiate meetings and support the development of the RFP pipeline for the Sales Directors. Responsible for developing relationships with clients to expand portfolio with new and existing clients in partnership with the Sales Directors. Supports and operationalizes the Sales team by: Reviewing each sales territory with the designated Sales Manager to identify new and existing targets where penetration and contact is required, enabling the expansion of eHealth solutions. Supporting each defined territory in the priority defined with the Sales Directors to prepare and initiate call plans, support email targeting campaigns and deliver thought leadership pieces which help drive new meetings and enable RFP inclusion. etc. | 8/11/2020 |
| 10350 | PTC Therapeutics South Plainfield, NJ Research Associate II, Pharmacology MS in biology Exp: 1+ year(s) |
The Research Associate II, Pharmacology is responsible for conducting scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in maintaining multiple mouse colonies, genotyping process, breeding, and conducting behavioral studies The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. The Research Associate II, Pharmacology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. Primary duties/responsibilities: Under general guidance, executes experiments and communicates results as part of multi-disciplinary team(s). Applies relevant scientific principles and techniques to research problems. Maintains detailed laboratory notebooks. Maintains knowledge of state-of-the-art principles and techniques. etc. | 8/11/2020 |
| 10351 | Biogen Cambridge, MA Associate Scientist II, Technical Development MS in biology, molecular biology, biochemistry or related Exp: 0-3 years |
We are seeking a highly motivated individual with mammalian cell culture experience, a background in molecular or cellular biology, and a strong interest in automation to join our Cell Line Development Team. Our group is focused on generating industry-leading cell lines for clinical and commercial programs. The candidate’s goals will be to engineer highly productive cell lines that enable fast-tracked program timelines that rely upon plasmid construction, transfection, cloning, high-throughput cell culture platforms, and ambr bioreactors. Additionally, the individual will be empowered to explore technology improvements geared toward advancing efficiency, with special consideration given to candidates with experience or passion for working with automation for custom needs as we push to expand throughput, implement novel production cell lines, develop continuous screening and integrate multi-level omics understanding. etc. | 8/11/2020 |
| 10352 | Biogen Research Triangle Park, NC Patient Services Coordinator BS/BA Exp: 1-2 year(s) |
The primary role of the Patient Service Coordinator is to facilitate the customer lifecycle by assisting patients, healthcare providers and others with activities related to starting and staying on therapy. Patient base includes both newly diagnosed and existing Alzheimer patients. Daily interactions involve contact via phone not only with patients but also health care providers, Biogen field force representatives, business service partners, nursing services and other internal work groups. The competitive candidates will have an ability to utilize strong interpersonal skills that will allow for the support and education of patients in their disease state, understanding of medical benefits, Biogen product education and the offering of service option explanations. etc. | 8/11/2020 |
| 10353 | Biogen Cambridge, MA Engineer I, Pilot Upstream, Gene Therapy BS/MS in bioengineering, biochemical engineering, biochemistry or related Exp: 0-2 years |
The successful candidate will join a team of scientists responsible for the development of scalable cell culture and purification processes used for the clinical and commercial manufacturing of adeno-associated virus (AAV) gene therapy vectors. Success in this position will require the candidate to independently plan and execute projects and experiments across multiple viral vector and precursor production platforms to support pilot-scale material generation runs and to effectively collaborate with different groups within Gene Therapy and Process Development. Candidates must be motivated and innovative with exceptional analytical and communication skills. etc. | 8/11/2020 |
| 10354 | Biogen Cambridge, MA Associate Scientist III, Gene Therapy - Formulation and Drug Product Development MS Exp: 0-2 years |
As a member of Biogen’s Gene Therapy Drug Product development team, the candidate will be responsible for providing analytical, formulation and process development support for drug product development programs. Conducting laboratory studies, both in-house and through external contract laboratories is a requirement of the position. Candidate is expected to work collaboratively in a matrix environment with other members of the gene therapy development team. Essential Responsibilities: Execution of formulation and process development study protocols, stability and product characterization studies with adeno-associated viral vectors. Performing analytical characterization of study samples using various biochemical or biophysical methods. etc. | 8/11/2020 |
| 10355 | Biogen Cambridge, MA Associate Scientist II/III – Fluid Biomarker Assay Development MS Exp: 1+ year(s) |
The Fluid Biomarkers group (Section of Clinical Sciences) is seeking a creative and collaborative lab-based scientist engaged in targeted proteomics for the detection of proteins and metabolites in different biological matrices (including plasma, serum, CSF, urine, tissues. This role is required to develop and implement clinically robust LC-MS assays to support clinical programs across the Neurology portfolio. The successful candidate will be capable of multitasking and effective planning to consistently meet deadlines. Responsibilities: Targeted protein biomarker assay development using state of the art liquid-chromatography-mass spectrometry (LC-MS) platforms including nano-LC, orbitrap (Q-Exactive, Q-Exactive +, Q-Exactive HF/HFX, Fusion) and UPLC-QQQ MS (AB Sciex). Sample preparation (tissues and cell lysates) for protein quantification. Biotinylation and various bead-antibody conjugation techniques. etc. | 8/11/2020 |
| 10356 | Biogen Cambridge, MA Associate Scientist II, Gene Therapy - Cell Line Technology BS in biology Exp: 1 year |
The successful candidate will work efficiently with team members and independently to plan, conduct, analyze, and document experiments to drive innovation in a cutting-edge modality. Qualifications: Team player with ability to execute tasks independently. Skilled molecular biologist (cloning, PCR, plasmid generation). Experience with mammalian cell culture (aseptic technique, proficiency with suspension cell culture, and experience with high-throughput cell culture desired). Proven track record of successfully planning, executing, and troubleshooting projects and experiments. Demonstration of strong organizational skills. Excellent written and verbal communication skills. etc. | 8/11/2020 |
| 10357 | Biogen Research Triangle Park, NC Mechanic II, Maintenance (Drug Product Facility) BS/BA Exp: 1 year |
Major Responsibilities Include: Collaborate with Responsible Engineers and Manufacturing personnel to troubleshoot equipment problems. Provide customer-oriented service and support in a fast-paced manufacturing environment. Sterile Filling equipment Isolators, Cartoner, labeling, Ink Jet Printers Automatic Vial Inspection equipment. Suggest practical changes or improvements to equipment and department work practices. Complete all assigned corrective work orders and Preventative Maintenance work with attention to detail and maintaining required GMP documentation. Follow Standard Operating Procedures in performance of assigned duties. Support manufacturing operations 12/7. etc. | 8/11/2020 |
| 10358 | Gyroscope King of Prussia, PA IT Technical Support Engineer BS/BA Exp: Epxerience in Windows 10/MAC oerations |
Help with triaging and setting up hardware (Laptops, printers, Lab systems) and supporting software including Office365, Okta and other platforms we use. We’ll need you to be the lead person to work with third party service providers to ensure end to end support is maintained for our office and remote stall working from home. | 8/9/2020 |
| 10359 | Halozyme San Diego, CA Staff Accountant 1, Accounts Payable Bs/BA in accounting or finance Exp: 1 year in accounts payable |
The Staff Accountant 1, Accounts Payable responsibilities include processing a full cycle accounts payable, processing travel and expense reimbursements, month end accruals and reconciling designated general ledger accounts. He/She will interface with multiple departments and personnel from within the organization. | 8/9/2020 |
| 10360 | Harpoon Therapeutics South San Francisco, CA Clinical Research Associate BS/BA in sciences or health care discipline Exp: 1-2 years in oncology/orphan drug development |
Maintain and/or accelerate timelines for achieving clinical operational milestones. Serve as the primary liaison with research sites; monitor the day-to-day conduct of the study, and resolve problems associated with the study; provide administrative and logistical support as needed. Ensure that documentation from investigators and investigational sites meets FDA/GCP/ICH requirements | 8/9/2020 |
| 10361 | Harvard Bioscience Holliston, MA Manufacturing Engineer BS/BA Exp: 0-2 years in electro-mechanical assemblies |
The qualified candidate will work within a multi-disciplinary team of engineers on DFM, cost reduction, and transfer to production activities. Work closely with assemblers and production leaders to improve manufacturability. Investigate quality issues for engineering improvements. Work closely with operations on design improvement and continuous improvement initiatives. | 8/9/2020 |
| 10362 | Helix San Diego, CA Clinical Laboratory Technician - 3rd Shift (CLT) (Temporary) Bs/BA in biological or health sciences Exp: |
We are searching for a highly motivated and team-oriented Clinical Laboratory Technician (CLT) to support a wide variety of molecular biology, biochemical, and extraction techniques to support projects focused on viral infection. Perform specimen processing and accessioning. Perform Automated RNA extraction. Perform PCR-based genetic testing in accordance with standard operating procedures. | 8/9/2020 |
| 10363 | Helix San Diego, CA Automations Engineer (Temporary) BS/BA in biological sciences or engineering Exp: 0-2 years |
Support production team by providing on site and immediate diagnostics of liquid handler issues/errors. Provide support for calibration, maintenance, and repair of liquid handling systems. Provide documentation of service, repair or maintenance of liquid handling systems | 8/9/2020 |
| 10364 | Helix Bind Boxborough, MA AssEMBLY TECHNICIAN HS Diploma/GED Exp: 0-2 years |
Prior experience not required, however, candidates with familiarity with any industrial assembly and/or machine shop equipment such as saws, drills, electronics soldering, and working with small/miniature machined components, will be given preference. Capable of reading and understanding technical specifications of a mechanical capacity. | 8/9/2020 |
| 10365 | Helix Bind Boxborough, MA Mechanical / Biomedical / Instrumentation ENGINEER BS/BA in engineering Exp: 0-5 years |
Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements using both internal and external technical resources. Assemble and test mechanical components for improving instrument functionality. Design test fixtures based on R&D, manufacturing, and quality requirements. | 8/9/2020 |
| 10366 | Helix Bind Boxborough, MA Engineering/Service Technician BS/BA, Associates, or Trade certification Exp: 0-2 years in electrical, mechanical installation |
The Engineering Technician will work to maintain, troubleshoot and repair medical diagnostic instruments, commission new equipment, through quality service and professionalism. We are seeking hard working, motivated, and well-organized individuals with a focus on continuous product improvement to exceed expectations. | 8/9/2020 |
| 10367 | Helomics Pittsburgh, PA Medical Laboratory Technologist BS in biological sciences Exp: 1+ years in lab |
The technologist is required to maintain and demonstrate cross-functional skills across all areas of the clinical lab. The technologist will be expected to successfully interface cross-departmentally with the Clinical Information Management, Client Services and LIMS groups to ensure the execution of the correct testing for all patients. These interactions will require a thorough knowledge of laboratory/scientific techniques and regulatory requirements including accreditation and governmental regulations. | 8/9/2020 |
| 10368 | Hemacare Northridge, MA Research Production AssociateI BS/BA in biological sciences Exp: 1 year in general lab experience |
This position isresponsible for the evaluationof humanblood products for manual orautomated cell isolations, product manufacturer,andcell culture.Perform QC testing and create a certificateof analysis(COA)for products manufactured. Record isolation details on a processing worksheet usinggood documentation practices. Operate flow cytometer and basic lab equipment. | 8/9/2020 |
| 10369 | Heska Loveland, CO Accounts Receivable Clerk I HS Diploma/GED Exp: 6 months |
Under the direct supervision of the AR Supervisor, the Accounts Receivable Clerk I will answer and responds to incoming customer calls and email requests. This position will regularly assist with making outbound calls to past due accounts as well as invoice processing, filing and sorting monthly statements, as needed. | 8/9/2020 |
| 10370 | Hexagon Bio Menlo Park, CA Research Associate, Molecular Biology BS in molecular biology Exp: 1+ year in industry |
As a Research Associate you’ll operate Hexagon's fungal genome discovery and molecular building block synthesis workflows, core parts of Hexagon’s pipeline which allow us to mine environmental samples for novel fungal genomes and retrieve individual biosynthetic genes to study further. You’ll apply and develop your skills running molecular and microbiological production protocols to operate and refine these pipelines using Hexagon’s suite of specialized robotic and software tools. | 8/9/2020 |
| 10371 | High Point Clinical Trials Center High Point, NC Research Nurse LPN/RN or diploma in nursing Exp: 1 year in practical nursing |
Assist in conduct of clinical studies. Provides licensed nursing coverage for studies and performs procedures as allowed by training and delegation. Assist in the conduct of clinical studies while providing licensed coverage. Performs all job responsibilities in accordance with standards of Good Clinical Practice (GCP), clinic standard operating procedures (SOP’s), and OSHA guidelines. | 8/9/2020 |
| 10372 | High Point Clinical Trials Center High Point, NC Lab Supervisor BS/BA preferred Exp: 1 year in lab |
Applicants should have demonstrated team management skills as well as working knowledge of IATA sample shipment processes, CLIA-waivered laboratory processes, and ability to fully manage external vendors for our clinical trial testing needs. This position ensures the full reconciliation of all specimens submitted to outside client and vendors in a manner fully compliant to Good Clinical Practice under FDA guidelines. | 8/9/2020 |
| 10373 | HighRes Biosolutions Beverly, MA Field Service Engineer BS in mechanical/electrical engineering Exp: 1-2 years |
As a Field Service Engineer, you are responsible for commissioning and calibrating laboratory automation devices to meet internal and customer specifications. As a qualified candidate, you will have mechanical debugging skills, knowledge of machine components, and a basic understanding of liquid handling software. Experience servicing and performing QC on automated liquid handlers is required. You’ll work closely with software and electrical engineers to commission, perform QC and trouble shoot instrumentation in the field. This position will involve travel to customer sites when needed. | 8/9/2020 |
| 10374 | Hitachi Chemical Advanced Allendale, NJ QC Microbiology Associate I BS/BA in sciences Exp: 0-1 years in environmental monitoring |
The Quality Control Microbiology Associate I serves as a support role to clinical and commercial production The QC Microbiology Associate will assist environmental monitoring activities to ensure that quality standards are upheld for all products produced at the facility. | 8/9/2020 |
| 10375 | Homology Medicines Bedford, MA Research Associate - Molecular Analytical Development (6 Month Contract) MS in biological sciences Exp: 0-4 years |
The individual in this role will be a talented and motivated technician who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. This is a largely laboratory-based position with a focus on providing analytical support for characterizing research-grade vectors. | 8/9/2020 |
| 10376 | Homology Medicines Bedford, MA Research Associate, Upstream Development - Pilot Plant Bs or MS in biological/chemical engineering or sciences Exp: 0-3 years |
The individual in this role will be highly motivated, enthusiastic and brings rigor and a desire to deliver on tasks with focus on the development and scale up of cell-based methods for producing AAV vectors. We seek candidates with proven ability to work independently after initial training and collaboratively to achieve optimized project plans, with the goal to deliver products that transform the lives of patients. | 8/9/2020 |
| 10377 | HotSpot Monmouth Junction, NJ Associate Biologist, DNA-Encoded Library Group BS or MS in biochemistry or related Exp: 0-4 years |
Characterize protein stability and function. Quantitate and characterize DNA. Perform DEL selections. Evaluate DEL hits. Use SOPs, protocols, and other documentation | 8/9/2020 |
| 10378 | Hovone Hovione, NJ Process Engineer BS in chemical science or engineering Exp: 1-3 years in industrial operations |
At Hovione, a Process Engineer's job mission is to ensure the best process engineering knowledge is applied in scaling up chemical and spray drying projects to maximize customer satisfaction ad Hovione's interests and in compliance with all Federal, State, Local and internal policies. It also includes the development of process engineering technical skills to increase the knowledge and offering on the best and state of the art technologies used in the industry. | 8/9/2020 |
| 10379 | HTG Tucson, AZ Helpdesk Technican Working towards degree in comp sci or IT Exp: 1+ years |
The Helpdesk Technician’s primary responsibility is to manage all daily operations of the Helpdesk, including but not limited to troubleshooting and resolving inbound tickets, collecting additional information, documenting steps taken, and escalating to other Information Technology team members. The Helpdesk Technician will be challenged to research new issues and increase working knowledge of IT systems through on the job training and mentorship. | 8/9/2020 |
| 10380 | Hemosconics Durham, NC Cartridge Automation Technician BS/BA Exp: 1 year in regulated manufacturing environment |
Setup and Shutdown of all equipment associated with the automation line per applicable Work Instruction. Operation of automation equipment in a controlled manufacturing environment. Completion of batch-related documentation in a timely manner and in accordance with regulatory requirements. | 8/9/2020 |
| 10381 | Harpoon Therapeutics South San Francisco, CA Clinical Trial Assistant BS/BA in biological sciences Exp: 1 year in clinical research |
Maintain and/or accelerate timelines for achieving clinical operational milestones. File, track and maintain study activity. Manage and ensure the paper and electronic Trial Master File (eTMF) meets FDA/ICH/GCP requirements. Coordinate execution of Non-Disclosure and Confidentiality Agreements (NDAs and CDAs) with study sit | 8/9/2020 |
| 10382 | Harpoon Therapeutics South San Francisco, CA Research Associate, Protein Expression BS/BA or MS in biological sciences Exp: BS: 1-5 years, MS: 1-3 years |
Stable and transient transfections of mammalian cell lines. Cryopreservation of cell lines and clarification of conditioned medium. SDS-PAGE, Octet BLI, and Western blot analysis of purified proteins. Materials management and inventory database maintenance. Maintenance of electronic lab notebook and databases, preparation of reports, and regular presentations to summarize results and update management | 8/9/2020 |
| 10383 | Bachem Torrance, CA Analytical Scientist - Method Development & Validation MS in analytical chemistry or related Exp: 1+ year(s) |
The Analytical Scientist will fulfill a critical role in GMP operations. This individual helps with the execution of feasibility evaluation of analytical methods, method development and validations, writing of validation protocols, reports and other technical quality documents; conducts validation related investigations and contributes to improvements in laboratory operations. Your Tasks: Independently plan and execute validation studies for test methods. Implement and perform analytical method transfer to Quality Control Department. Write validation protocols and final reports, test methods, standard operating procedures, and technical reports. Under minimal supervision, conduct and document investigations related to validation activities. etc. | 8/5/2020 |
| 10384 | Bachem Torrance, CA QA Specialist I (Document Control) BS in science or related Exp: 1+ year(s) |
The Quality Assurance Specialist I (Document Control) fulfills a critical role for Quality Assurance. The primary function of this individual will support all activities related to the Document Control function, including the review and release of SOPs, Forms, Specifications, Batch Records, Plans, Protocols, Reports, etc. through Master Control. This individual will support record management ensuring that the site stays in compliance with FDA and international regulatory requirements. Your Tasks: Review and process all submitted documents through Master Control System in a timely manner, meeting monthly, quarterly and annually department goals. Issue logbooks, active and retired documents as required to meet department goals. etc. | 8/5/2020 |
| 10385 | Bachem Vista, CA Chemist I BS in chemistry or related Exp: 1-3 year(s) |
The Chemist (Chem1) function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. Your Tasks: Perform synthesis process including solution phase and solid phase peptide synthesis, peptide resin cleavage, resin cleavage with HF or other chemical cocktails. Perform purification process by chromatography, crystallization and other techniques, and in-process test method. Follow approved GMP manufacture directions such as Master Batch Records, Standard Operation Procedures, Standard Test Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities. etc. | 8/5/2020 |
| 10386 | Bachem Torrance, CA Production Chemist I BS in chemistry or related Exp: 1-3 year(s) |
The Chemist (Chem1) function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. Your Tasks: Perform synthesis process including solution phase and solid phase peptide synthesis, peptide resin cleavage, resin cleavage with HF or other chemical cocktails. Perform purification process by chromatography, crystallization and other techniques, and in-process test method. Follow approved GMP manufacture directions such as Master Batch Records, Standard Operation Procedures, Standard Test Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities. etc. | 8/5/2020 |
| 10387 | Bachem Torrance, CA Production Technician AS in chemistry or related science Exp: 0-2 years |
The Production Technician I performs an integral role as part of the Production team at Bachem. This role is responsible for contributing to the safe and economic manufacture of active pharmaceutical ingredient (API) products, such as peptide or related bioorganic compounds, as a member of a production team. As a Production Technician I, you will be producing APIs from gram to multiple kg scale. The majority of responsibilities will include routine synthetic organic synthesis, the operation of manufacturing equipment and keeping track of batch documentation according to cGMP regulations. etc. | 8/5/2020 |
| 10388 | BardyDx New Jersey, NJ Holter Analysis Technician HS diploma/AS/AA Exp: 1-3 year(s) |
Currently, we are looking for Holter Analysis Technicians to join our Clinical Services Team who are passionate about cardiac rhythms and helping cardiac patients through our innovative remote patient monitoring body sensor technologies. The right individuals will join a dynamic and fast-paced start-up environment. Ideal candidates will have CCT or CRAT certification or specialize in cardiac rhythm recognition and interpretation skills. Experience with cardiology or electrophysiology can be advantageous. This position requires PC proficiency, excellent written and verbal communication skills, and meticulous attention to detail. etc. | 8/5/2020 |
| 10389 | Baxter Opelika, AL Quality Lab Tech I BS in chemistry or biological sciences Exp: 0-2 years |
Performs required tests in the performance, microbiological, and chemical labs on finished dialyzers and raw materials to support product acceptance. This includes performing analyses, calibrations and maintenance on multiple lab equipment/instruments and entering results in MES. May assist with environmental and process media monitoring by taking samples and testing as required by defined procedure. Maintains cleanliness of labs and lab instruments. Analyze issues on out of specification (OOS) conditions and unusual trends and immediately initiate NCR or deviation and notify Lab Supervisor/Quality Engineer and/or QRM Manager. Orders and maintains lab supply stock (reagents, chemicals, standards etc.) to maximize efficiency. etc. | 8/5/2020 |
| 10390 | Baxter Round Lake, IL Research Associate I BS Exp: 1-3 year(s) |
Essential Duties and Responsibilities: Perform microbiology testing in support of medical device and pharmaceutical projects. Record data and assist in the preparation of documentation using Good Documentation Practices (GDP). Support the maintenance of microbiological laboratories and equipment. Understand and apply applicable corporate and divisional Standard Operating Procedures (SOP). Under direction, conduct routine research and/or developmental activities. Plan details of assigned tasks within specific parameters. etc. | 8/5/2020 |
| 10391 | Baxter Alliston, ON Associate I, Quality Operations BS in microbiology, chemistry, biological sciences, or engineering Exp: 1-3 year(s) |
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. | 8/5/2020 |
| 10392 | Baxter Alliston, ON Associate I, Quality Operations - Nights BS in microbiology, chemistry, biological sciences, or engineering Exp: 1-3 year(s) |
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. | 8/5/2020 |
| 10393 | Baxter Alliston, ON Associate I, Quality Operations - Weekend Days BS in microbiology, chemistry, biological sciences, or engineering Exp: 1-3 year(s) |
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. | 8/5/2020 |
| 10394 | Baxter Alliston, ON Associate I, Quality Operations - Weekend Night BS in microbiology, chemistry, biological sciences, or engineering Exp: 1-3 year(s) |
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. | 8/5/2020 |
| 10395 | Arthrex Naples, FL Engineering Tech - Sutures AS/BS Exp: Not necessary for AS/BS candidates |
Responsible for supporting the Engineering department by assisting engineers with the lifecycle development of medical devices, including new product development and maintenance of released products. Essential Duties and Responsibilities: Generate and maintain mechanical models and drawings utilizing computer aided design (CAD) program, according to specifications determined by the engineer. Assist in the testing of design prototypes and support R&D testing activities of assigned products as assigned. Support design changes to develop and improve products as well as facilitate manufacturing operations. Support QA, Manufacturing, Regulatory, Marketing, Suppliers, and Product Management as assigned. Assist with various aspects of the engineering product development process as assigned. etc. | 8/4/2020 |
| 10396 | Arthrex Ave Maria, FL Clean Room Assembler HS diploma or equivalent Exp: 6+ months |
Main Objective: To assemble, label and package medical devices. Essential Duties and Responsibilities: Performs manual and fixture assisted device assembly and packaging on medical device components, kits, convenience packs and / or any clean room specific device assembly as assigned. Performs placement of components onto the blister trays and die cut restraints. Performs label application onto packaging constructs. Performs supplemental label application, blister loading, pouch and blister sealing and visual seal inspection. Load and orient unit devices into unit packages and / or automated equipment. etc. | 8/4/2020 |
| 10397 | Arthrex Sandy Springs, SC QC Inspector II - Night Shift HS diploma or equivalent Exp: 1 year |
Performs a variety of quality control test and inspection functions on materials, components and finished goods at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products. Essential Duties and Responsibilities: Performs and documents dimensional inspections on inventory parts using engineering prints, Inspection procedures or work instructions. Selects products for tests at specified stages in production process, and tests products for variety of qualities, such as dimensions, performance, and mechanical, electrical, or chemical characteristics. Records test data, applying statistical quality control procedures. May perform, as needed, nondestructive tests on materials, parts, or products to measure performance, life, or material characteristics. etc. | 8/4/2020 |
| 10398 | Ascent Pharmaceuticals Central Islip, NY Quality Control Chemist MS in pharmacy or chemistry Exp: 1 year |
Ascent seeks Quality Control Chemist in Central Islip, NY to scientifically analyze and test raw materials, in-process and finished product samples using modern quality control techniques; develop, validate and test analytical methods for analytical pharmaceutical ingredients (API) and dosage forms; perform quality control/development activities using Chromatography, Spectroscopy, HPLC, GC, TLC, Dissolution etc.; work with advanced analytical equipment like HPLC, GC, DSC and IR and apply knowledge of broad variety of quality control and analytical techniques; validate and analyze results as per regulatory standards such as USP, BP, EP, ICH and USFDA; develop, implement and maintain QC systems and activities; perform in-process inspection, document results and perform a wide variety of inspections, checks, tests and sampling procedures for the manufacturing process; etc. | 8/4/2020 |
| 10399 | Assembly Bio Groton, CT Research Associate I / II, Drug Substance Process Development (Microbiome) BS/MS in a life science Exp: 0-2+ years |
The Research Associate I / II, Drug Substance Process Development (Microbiome) will serve as a key team member in the development and qualification of robust processes for production of human commensal bacteria suitable for use as therapeutic agents. The individual will participate in the design, independent execution of experiments and perform data analysis relating to cell banking, fermentation, harvest, and freeze-drying processes. Execution of analytical testing to support rapid data generation would be desirable. It is expected that the individual will work closely with Research, Drug Product Development, Manufacturing, Analytical Development, Quality Control, and Quality Assurance to ensure timely delivery against team and corporate objectives. (S)he will play an important role in the transfer of formulations and processes as well as facilitating phase-appropriate scale-up operations. etc. | 8/4/2020 |
| 10400 | Astella South San Francisco, CA Research Associate II, Cell Biology MS Exp: 0-2 years |
The primary purpose of the Research Associate II is to support all cell biology and assay development needs. This position will work primarily in a laboratory setting with Scientist and R&D teams. Essential Job Responsibilities: Culturing of both established cell lines and primary (e.g. human T cells) cell cultures. Generation and quality control assessment of lentivirus to support R&D work. DNA purification to support lentiviral production; additional molecular biology experience (e.g. PCRs, molecular cloning) a plus. etc. | 8/4/2020 |
| 10401 | Astella South San Francisco, CA Research Associate II, Protein Purification MS Exp: 0-2 years |
The primary purpose of this role is to support all protein production, purification, and quality control assay needs. This position will work primarily in a laboratory setting with Scientist and R&D teams. If candidate skillset is extended to operational sufficiency with Akta chromatography and Octet kinetic analysis systems then would qualify for Sr. Research Associate role. Essential Job Responsibilities: Culturing and maintenance of established cell lines; transfection of DNA into cell lines for target protein expression. Demonstrated competency with standard protein purification strategies (e.g. protein A, Ni-NTA purification, on-column protease cleavage strategies). etc. | 8/4/2020 |
| 10402 | Astella Seattle, WA Research Associate II, Analytics MS Exp: 0-2 years |
The primary purpose of Research Associates working in Analytics (RA II and Senior RA) for our Core Technologies Department is to support the molecular engineering of our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to develop molecular and cellular assays to characterize our proprietary Universal Donor Cells. Essential Job Responsibilities: Developing and routinely executing standard analytical assays including genotyping PCR/qPCR and flow cytometry. Performing standard molecular biology techniques including primer design, molecular cloning, and Sanger sequencing. etc. | 8/4/2020 |
| 10403 | Astella Seattle, WA Research Associate II, Cell Editing MS Exp: 0-2 years |
Essential Job Responsibilities: Designs and executes AAV-mediated gene-editing of pluripotent stem cells in a controlled manufacturing environment. Performs data collection, analysis and interpretation for stem cell culture and gene-editing processes. Participates in group meetings and regularly presents at cross-functional team meetings. Prepares and reviews the work of others, including but not limited to, technical slide decks, reports, Standard Operating Procedures (SOPs) and production batch records. May serve as a technical resource for preparation of regulatory filings. Supports Process Development to transfer manufacturing processes. etc. | 8/4/2020 |
| 10404 | Astella Seattle, WA Research Associate I, Process Development BS Exp: 0-3 years |
Universal Cells carries out clinical-grade AAV-mediated gene-editing of pluripotent stem cells. The Research Associate I Process Development will work as part of a team evaluating processes, and planning/executing experiments to evaluate all aspects of culturing, gene-editing, and processing of pluripotent stem cells. The Research Associate will be formally trained and will perform all fundamental skills including record keeping, general lab skills, equipment use and maintenance, aseptic technique/cell culture, and basic troubleshooting. They will assist with projects and lead day-to-day activities based on abilities. They will keep appropriate documentation, including lab notebooks, batch documentation and experimental summaries. etc. | 8/4/2020 |
| 10405 | Astella Seattle, WA Research Associate II, Core Technologies MS Exp: 0-2 years |
The primary purpose of Research Associates working (RA II and Senior RA) for our Core Technologies Department is to support the molecular engineering of our gene edited Universal Donor Cells. They will work as a key team member on a fast-paced team to assist with Adeno-Associated Virus production and the development and execution of molecular assays to characterize our proprietary gene edited cells. Essential Job Responsibilities: Performing plasmid DNA isolation and producing Adeno-Associate Virus under controlled conditions following SOPs and with detailed real-time documentation. Routinely performing standard molecular biology techniques including primer design, molecular cloning, gDNA isolation, PCR, and Sanger sequence analysis. etc. | 8/4/2020 |
| 10406 | AstraZeneca Gaithersburg, MD R&D Associate I/II - Purification Process Sciences BS/MS in biochemistry or chemical engineering or related Exp: 0-2+ years |
The successful candidate will: Develop and characterize downstream processes for the manufacture of biopharmaceuticals (monoclonal antibodies and other proteins) in late stage clinical development through commercial launch. Be responsible for a portion of a purification development project. Make observations, analyze data and interpret results. Maintain accurate records of experimental results, review, analysis, and interpretation of experimental data. Make periodic presentations in group meetings, project team meetings, and in one-on-one situations. Prepare/review development reports, tech transfer and process validation documents, regulatory submissions. etc. | 8/4/2020 |
| 10407 | Atreca South San Francisco, CA Research Associate or Senior Research Associate, Protein Engineering MS in cell biology, molecular biology, immunology or bioengineering Exp: Not necessary for MS candidates |
We are seeking a motivated and enthusiastic Research Associate or Sr Research Associate to join our Protein Engineering group. The successful candidate will play a key role in further developing our yeast display platform and applying it to engineer antibodies and bispecifics. Duties & Responsibilities: Culture yeast and perform flow cytometry assays. Sort libraries by FACS and help with NGS sample preparations (plasmid prep and PCR). Help develop methods for selecting yeast-displayed antibodies bound to cancer cells. Follow laboratory safety guidelines and practices. etc. | 8/4/2020 |
| 10408 | Atum Newak, CA Mammalian Tissue Culture Associate BS in cell biology Exp: 1+ year(s) |
This an entry-level position within our protein group. The ideal candidate will be responsible for maintenance of mammalian cell culture stocks, transfection of cell cultures expressing a variety of protein types including therapeutic proteins, antigens and assay reagents. They will not be satisfied with just doing their part but being part of a collaborative team that aims to continually improve. Responsibilities of the position: Tissue Culture: Maintain various mammalian cell lines using sterile techniques; transiently transfect cell cultures for the generation of recombinant proteins; determine cell counts and cell viability using microscope and automated cell counting devices. Monitor metabolites and macromolecular products and take endpoint measurements that could include western blotting an titer measurement using ForteBio Octet. etc. | 8/4/2020 |
| 10409 | Atum Newak, CA Protein Purification Associate (Mammalian) BS in biology or related Exp: 1-3 year(s) |
This an entry-level position within our mammalian protein purification group. The ideal candidate will be responsible for purification and characterization of a variety of protein types including therapeutic proteins, antigens and assay reagents expressed in mammalian cells. They will not be satisfied with just doing their part, but will thrive on being part of a collaborative team that aims to continually improve. Proteins will be purified at various scales ranging from high throughput robotic purification to many grams. Additionally, the incumbent will have opportunities to learn cell culture, bacterial and yeast fermentation in addition to bioanalytical techniques. etc. | 8/4/2020 |
| 10410 | Boston Scientific Arden Hills, MN Quality Engineer I BS Exp: 0-2 years |
The Quality Engineer I will provide Quality/Process Engineering support to the Cardiac Rhythm Management and Neuromodulation and potentially other businesses to ensure delivery of the highest quality product to the customer. They will partner with manufacturing and operations to provide quality engineering support and the highest quality of our products. This position may also provide quality engineering support to additional manufacturing lines as necessary. Your Responsibilities Will Include: Reduces and controls process defects (scrap, nonconforming material, customer complaints) by leading efforts and cross-functional teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for implementing product stops & documenting release criteria. Develops and implements product quality plans, documents and systems by creating product specifications, quality specifications, quality plans, risk analysis, FMEAs in conjunction with other product development team members. May be responsible for risk analyses and FMEAs. etc. | 8/4/2020 |
| 10411 | Boston Scientific Arden Hills, MN Manufacturing Technician III (1st Shift) AA Exp: 1-3 year(s) |
With general supervisory direction, you will be responsible for performing support functions for manufacturing operations, including troubleshooting equipment and process issues, and performing and documenting machine maintenance procedures. Additionally, it is expected that you will partner with engineering in developing methods and procedures to control or modify manufacturing processes. Your Responsibilities Will Include: Identify and troubleshoot process, material or equipment problems to minimize down time. Perform preventative maintenance and calibration procedures, as well as author equipment maintenance and calibration procedures. Modify existing and develop new tooling and fixtures. Revise existing documents, processes, and/or methods to correct or improve processes/product. etc. | 8/4/2020 |
| 10412 | Boston Scientific Maple Grove, MN Machine Operator I - 3rd Shift - Maple Grove--Grinding HS diploma/AS/AA Exp: 1 year |
Your Responsibilities Include: Understands and adheres to safety policies and practices. Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Gains basic understanding of Lean Manufacturing and related principles. Willing to flex and rotate as necessary and work well with all group members, both within the team and cross-functionally. Under the direction of other maintains accurate records such as Manufacturing Execution System (MES), Shop Floor Paperwork (SFP), training Records System (TRS), Product Data Management (PDM), Systems Application & Products (SAP) and Process Equipment Optimization (PEO). etc. | 8/4/2020 |
| 10413 | Boston Scientific Maple Grove, MN Machine Operator I - 1st Shift - Maple Grove--Grinding HS diploma/AS/AA Exp: 1 year |
Your Responsibilities Include: Understands and adheres to safety policies and practices. Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Gains basic understanding of Lean Manufacturing and related principles. Willing to flex and rotate as necessary and work well with all group members, both within the team and cross-functionally. Under the direction of other maintains accurate records such as Manufacturing Execution System (MES), Shop Floor Paperwork (SFP), training Records System (TRS), Product Data Management (PDM), Systems Application & Products (SAP) and Process Equipment Optimization (PEO). etc. | 8/4/2020 |
| 10414 | Boston Scientific Maple Grove, MN Manufacturing Technician I (3rd Shift) AA Exp: 0-1 year(s) |
With general supervisory direction, you will be responsible for performing support functions for manufacturing operations, including troubleshooting equipment and process issues, and performing and documenting machine maintenance procedures. Additionally, it is expected that you will partner with engineering in developing methods and procedures to control or modify manufacturing processes. Your Responsibilities Will Include: Identify and troubleshoot process, material or equipment problems to minimize down time. Execute validation plans and compile data. Collect data and perform basic statistical analysis for process characterization and scrap reduction goals. etc. | 8/4/2020 |
| 10415 | Boston Scientific Arden Hills, MN Manufacturing Technician I (3rd Shift) AA Exp: 0-1 year(s) |
With general supervisory direction, you will be responsible for performing support functions for manufacturing operations, including troubleshooting equipment and process issues, and performing and documenting machine maintenance procedures. Additionally, it is expected that you will partner with engineering in developing methods and procedures to control or modify manufacturing processes. Your Responsibilities Will Include: Identify and troubleshoot process, material or equipment problems to minimize down time. Execute validation plans and compile data. Collect data and perform basic statistical analysis for process characterization and scrap reduction goals. etc. | 8/4/2020 |
| 10416 | Boston Scientific Maple Grove, MN Machine Operator I - 2nd Shift - Maple Grove--Grinding Job HS diploma/AS/AA Exp: 1 year |
Your Responsibilities Include: Understands and adheres to safety policies and practices. Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Gains basic understanding of Lean Manufacturing and related principles. Willing to flex and rotate as necessary and work well with all group members, both within the team and cross-functionally. Under the direction of other maintains accurate records such as Manufacturing Execution System (MES), Shop Floor Paperwork (SFP), training Records System (TRS), Product Data Management (PDM), Systems Application & Products (SAP) and Process Equipment Optimization (PEO). etc. | 8/4/2020 |
| 10417 | Avion Pharmaceuticals Wichita Falls, TX Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Rheumatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 8/4/2020 |
| 10418 | Avion Pharmaceuticals Tallahassee, FL Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Rheumatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 8/4/2020 |
| 10419 | Avion Pharmaceuticals Lynchburg, VA Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Rheumatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 8/4/2020 |
| 10420 | Avion Pharmaceuticals Cherry Hill, NJ Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Rheumatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 8/4/2020 |
| 10421 | Avion Pharmaceuticals Alphretta, GA Inside Sales Representative AS/AA/BS/BA Exp: 1 year |
The Inside Sales Representative/ Customer Service Associate will assist the Sales & Marketing function by building a rapport and strong relationships that are necessary to increase sales and product placement for Avion's product portfolio. We are looking for a positive and motivated individual who would be passionate about our company and product portfolio. The ideal candidate will also have excellent customer service, communication, and organizational skills. ESSENTIAL DUTIES AND RESPONSIBILITIES: Initiate introductory calls with the objective of developing a long-term business relationship with customer accounts (70% doctors and 30% pharmacies). Build, sustain & maximize customer relationships through timely routine contact with new and existing customers. etc. | 8/4/2020 |
| 10422 | Assembly Bio Groton, CT Contract Lab Technician I/II (Microbiome) AS/AA Exp: 0-2 years |
The Laboratory Technician I or II, Drug Substance Process Development (Microbiome) will provide support functions in the development and qualification of robust processes for production of human commensal bacteria suitable for use as therapeutic agents. The individual will assist laboratory operations by preparing media, equipment, and executing housekeeping duties such as autoclaving, according to written procedures. Documentation of these duties in laboratory notebook systems is expected. Key Responsibilities include: Follow written procedures for consistent and reliable preparation of complex media recipes. Documentation in laboratory notebook systems. etc. | 8/4/2020 |
| 10423 | Greenlight Biosciences Research Triangle Park, NC Research Associate – Plant Biology (Contract Position) BS in biology Exp: 1-2 years |
Collaboratively design and conduct plant phenotyping assays to determine treatment efficacy. Conduct molecular analyses of gene expression using PCR and RT-qPCR. Sow and maintain plants under a variety of conditions in chamber and greenhouse settings | 8/2/2020 |
| 10424 | Greenlight Biosciences Medford, MA Research Associate / Sr. Research Associate – Molecular Biology BS or MS in chemical/biological engineering or sciences Exp: 1-2 years in biotech/pharma |
he successful candidate will support ongoing high-throughput platform production and optimization in the context of several milestone-driven projects. Plan & perform routine molecular biology techniques such as PCR, DNA subcloning, in vitro transcription, cell transformation, cell culture, protein expression & purification, nucleic acid isolation as well as more advanced methods in support of research projects | 8/2/2020 |
| 10425 | Greenlight Biosciences Medford, MA Research Associate / Sr. Research Associate – Molecular Biology BS or MS in engineering or biological sciences Exp: 1-2 years in biotech/pharma |
Plan & perform routine molecular biology techniques such as PCR, DNA subcloning, in vitro transcription, cell transformation, cell culture, protein expression & purification, nucleic acid isolation as well as more advanced methods in support of research projects. Execute experiments and associated analytics (such as enzyme assays) at different scales (ranging from 10s of µLs to 10s of Ls) for debottlenecking & optimization and | 8/2/2020 |
| 10426 | Grifols Hattiesburg, MS Biomedical Technician HS Diploma/GED Exp: 6-12 montsh as medical assistant or phlebotomy training |
Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. | 8/2/2020 |
| 10427 | Grifols Memphis, TN Laboratory Quality Assurance Coordinators - 2nd Shift BS/BA in biological or chemical sciences Exp: 0-2 years |
This position is responsible for performing quality assurance functions in the laboratory, including the review of test records, reviewing records, monitoring employee practices, assessing activities for compliance to procedures, and keeping management informed of any quality concerns related to the laboratory operator. | 8/2/2020 |
| 10428 | Grifols Memphis, TN Laboratory Quality Assurance Coordinators - 1st Shift BS/BA in biological or chemical sciences Exp: 0-2 years |
This position is responsible for performing quality assurance functions in the laboratory, including the review of test records, reviewing records, monitoring employee practices, assessing activities for compliance to procedures, and keeping management informed of any quality concerns related to the laboratory operator. | 8/2/2020 |
| 10429 | Grifols Kingsport, TN Biomedical Technician HS Diploma/GED Exp: 6-12 montsh as medical assistant or phlebotomy training |
Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. | 8/2/2020 |
| 10430 | Grifols Asheville, NC Donor Processor HS Diploma/GED, medical technologist degree preferred Exp: 0-2 years |
This position is responsible for processing a potential plasma donor from their initial registration at the Source Plasma Center through various procedures and tests that are part of the screening to determine if the donor is suitable for plasmapheresis. | 8/2/2020 |
| 10431 | Grifols Houston, TN Donor Center Technician HS Diploma/GED Exp: 0-2 yearss, elgible for licensures |
Our ideal Donor Center Technician is a stand out colleague who is patient, can handle multiple tasks, and adapt to a dynamic work environment. Conducts pre-donation medical screening in accordance with established guidelines. You determine Hematocrit (HCT) and Protein via finger stick and use of the hematastat and refractometer. | 8/2/2020 |
| 10432 | Grifols Dothan, AL Biomedical Technician HS Diploma/GED Exp: 6-12 montsh as medical assistant or phlebotomy training |
Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. | 8/2/2020 |
| 10433 | Guardant Redwood City, CA Clinical Research Associate BS in biological sciences or medical speciality Exp: 1-2 years in clinical research |
The Clinical Research Associate l (CRA) is responsible for monitoring activities that will lead to successful execution of IVD clinical studies. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA engages with internal and external stakeholders as a member of the Clinical Trial Operations team. | 8/2/2020 |
| 10434 | Guardant Redwood City, CA Clinical Trials Assistant BS in biological related field Exp: 1 year in clinical research or GCP |
The Clinical Trial Assistant (CTA) is primarily responsible for the coordination of activities associated with the setup and management of clinical studies under the direction of, or as delegated by a member of the Clinical Trial team. Responsibilities will range from clinical study coordination to data entry projects and general office work. | 8/2/2020 |
| 10435 | Guardant Spring, TX Client Services Associate BS/BA Exp: 1 year in client experience |
CSA is responsible for receiving and responding to all types of communication: phone, email and web inquiries from customers (physician offices, laboratories, and hospitals), sales representatives and patients. Adhering to Standard Operating Procedures (SOP’s) pertaining to data entry and data verification requirements | 8/2/2020 |
| 10436 | Gritstone Oncology Cambridge, MA BIOREPOSITORY TECHNICIAN CONTRACTOR (Specimen Management) AS/AA or BS/BA in sciences or healthcare Exp: 1-2 years in lab setting |
The Biorepository Technician Contractor is directly responsible for supporting the manufacturing and research labs under the direction of the Translational Medicine Operations function at Gritstone. The Contractor performs a variety of tasks associated with the tracking, receipt, storage, maintenance and retrieval of biospecimens collected as part of Gritstone’s research programs. | 8/2/2020 |
| 10437 | GSK King of Prussia, PA Lead Automation Engineer - Facilities BS/BA in engineering, life sciences, biology Exp: 0-8 years |
Provide technical leadership in support of building & utility control systems and network infrastructure. Critical systems include Emerson DeltaV, Siemens BAS, and Rockwell PLCs. Collaborate with building stakeholders and vendors throughout the automation lifecycle: gather system/end user requirements; complete design, implementation, and testing/validation of changes; maintain documentation; maintain and monitor various site automation systems. | 8/1/2020 |
| 10438 | GSK St. Louis , MO Manufacturing Material Handler HS Diploma/GED Exp: 1-5 years in production |
Ensure quality and compliance in accordance with established procedures and standards of the Quality System. Locate finished tablets bins and correctly stage and issue bins as needed to support packaging department. Locate and transport raw materials to floors as needed. Collect, transport, and cleanout empty bins. Support the removal of trash and waste on an as needed basis. Fill blending dump stations as required. Fill preweigh intermediate bulk containers as required. | 8/1/2020 |
| 10439 | GSK St. Louis , MO Manufacturing Operator HS Diploma/GED Exp: 1-5 years in production |
Operate and troubleshoot a variety of machinery. Operate the worksaver and standup/sitdown lifts as needed. Utilize manlifts. Perform line changeovers, which include cleaning, disassembly, re-assembly of line equipment and lubrication. Comply with and support the GSK Environmental, Health and Safety policies and procedures. | 8/1/2020 |
| 10440 | GSK Lincoln, NE HVAC Technician (2nd Shift) Associates in HVAC technology Exp: 0-3 years |
As a GMP system owner, the HVAC Technician is responsible to maintain a compliant state, troubleshoot, inspect, repair and document work on core facilities equipment or systems that support the manufacture and packaging of over the counter, dietary supplement and medical device products. | 8/1/2020 |
| 10441 | GSK Richmond, VA Analytical Associate Scientist BS in chemistry Exp: 0-2 years |
As an Operational QA Staff, you will manage/lead/be responsible for working on the shop floor addressing quality issues during production shift operating hours. Additional responsibilities include supporting incident and deviation investigations, participation in internal auditing activities and batch record review. | 8/1/2020 |
| 10442 | Gliknik Baltimore, MD Laboratory Research Associate BS/BA in life sciences Exp: Entry Level |
Responsibilities include: reagent preperation, molecular biology work, experiments with aseptic cell cultures and protein pruification. Other responsibilities include completing appropriate documentation of experiments including laboratory notebooks, equipment logbooks and inventory forms, preparation of technical reports, summaries, protocols and quantitative analyses with minimal supervision. | 8/1/2020 |
| 10443 | GBT South San Francisco, CA CONTRACT – RESEARCH ASSOCIATE, PHARMACOLOGY BS in life sciences/engineering Exp: 0-2 years lab experience |
Perform in vivo pharmacology studies with hematological disease models and conduct in vivo drug efficacy studies to support early drug discovery projects. Develop and troubleshoot novel in vivo disease models for mechanism of action studies. Plan, execute, analyze, and document experiments | 8/1/2020 |
| 10444 | Globus Medical San Antonio, TX Manufacturing Technician HS Diploma/GED Exp: 1 year in manufacturing |
The Manufacturing Technician is responsible for performing human tissue processing activities in accordance with FDA regulations, AATB Standards and SOPs. Preparing sections of human tissue for surgical implantation. Utilizing special techniques, instrumentation, and equipment to evaluate, cut, shape, grind and package tissue to exacting specifications and protocols | 8/1/2020 |
| 10445 | Globus Medical San Antonio, TX Manufacturing Technician HS Diploma/GED Exp: 1 year in manufacturing |
The Manufacturing Technician is responsible for performing human tissue processing activities in accordance with FDA regulations, AATB Standards and SOPs. Preparing sections of human tissue for surgical implantation. Utilizing special techniques, instrumentation, and equipment to evaluate, cut, shape, grind and package tissue to exacting specifications and protocols | 8/1/2020 |
| 10446 | Gore Flagstaff, AZ Quality Control Unit Associate College degree Exp: 1 year minimum in manufacturing |
Ensuring appropriate cGMP documentation is generated, revised, approved and maintained. Reviewing associated documentation and labeling for accuracy and completeness. Verifying lot acceptance results for adherence to specification, limits or other acceptance criteria. Approving these results, as required | 8/1/2020 |
| 10447 | Grail Menlo Park, CA Research Associate 1/2 BS/BA in biological or chemical sciences Exp: 1-2 years in BSL2 labs |
As a Research Associate in GRAIL’s R&D Group, you will play an integral role in the development of technology and workflows for genomics-based clinical assays. The ideal candidate should be detail-oriented and have experience with blood processing, nucleic acid extraction, and strong molecular biology skills. | 8/1/2020 |
| 10448 | Grail Menlo Park, CA Process Engineer 1/2 (Equipment Qualification) BS or MS in biological sciences or engineering Exp: 1-4 years in process engineering/R&D in med/pharma |
Design and characterize new laboratory equipment qualification processes within an NGS setting. Participate in the development of product plans, evaluation of processes and process risk, and development of project timelines. Develop and execute qualification studies for new and existing equipment in accordance with ISO standards. | 8/1/2020 |
| 10449 | Grail Menlo Park, CA Core Services Research Associate 1/2 BS in relevant Exp: 1+ years in NGS |
Execute on forecasted R&D experiments ranging from reagent evaluation and qualification to general data generation activities. Execute on automated and manual sample preparation and NGS assays. Be responsible for accurately recording work performed per GLP, including results and methodology. | 8/1/2020 |
| 10450 | Grand River Grand Rapids, MI ASEPTIC MANUFACTURING ASSOCIATE 2ND SHIFT HS Diploma/GED Exp: 0-1 years in manufacturing |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. Follow production and manufacturing procedures. Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed. | 8/1/2020 |
| 10451 | Grand River Grand Rapids, MI QC Biochemist I BS/BA in chemistry Exp: 0-3 years in pharma |
Responsible for supporting quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients, excipients and finished pharmaceutical products. | 8/1/2020 |
| 10452 | Grand River Grand Rapids, MI Microbiology Technician BS/Ba in microbiology Exp: 0-2 years |
Supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. Performs sampling of water pure steam to support manufacturing activities. Performs Environmental Monitoring of aseptic filling rooms and supporting areas. | 8/1/2020 |
| 10453 | Grand River Grand Rapids, MI Mechanical Engineer BS/BA in engineering or sciences Exp: 1+ years in FDA regulated environment |
Assist the Grand River Aseptic Manufacturing Facilities & Engineering and Operations departments by specializing in facility and utility optimization and providing subject matter expertise on mechanical systems. Run projects and oversee construction activities. Demonstrate, build, and enforce the best practices for all engineering projects and functions within the facilities. | 8/1/2020 |
| 10454 | Grand River Grand Rapids, MI ASEPTIC MANUFACTURING ASSOCIATE - 3RD SHIFT HS Diploma/GED Exp: 0-1 years in manufacturing or lab environment |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. Follow production and manufacturing procedures. Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed. | 8/1/2020 |
| 10455 | Globus Medical Audubon, PA Regulatory Associate BS/BA in health or sciences, engineering is a plus Exp: 0-2 years in med devices |
The Regulatory Affairs Associate assists in drafting, submitting and gaining clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requiring working knowledge of products under review and of relevant regulations and guidance documents. | 8/1/2020 |
| 10456 | Abbvie Lake County, IL Pharmacy Technician HS diploma/AS/AA Exp: 1+ year(s) |
The Pharmacy Technician position exists to support the pharmacist(s) in completing the duties associated with entering and managing drug therapy orders, fulfilling, and dispensing prescriptions, maintaining pharmacy records and other professional activities. This position is responsible for collaborating with and supporting Pharmacy Leads and Supervisors in day to day activities, issue resolution, and completion of project tasks. Responsibilities: Assist the pharmacist with practice of pharmacy in accordance with federal, state and local regulations, HIPAA guidelines, corporate and departmental policies and procedures. Assist pharmacists in the picking, labeling, packing and shipping of orders; by accurately interpreting healthcare provider’s prescription orders and entering it into the core pharmacy system; etc. | 7/28/2020 |
| 10457 | ImmunityBio Louisville, CO Associate, Manufacturing Operations MS Exp: 1-3 year(s) |
The candidate is responsible for supporting manufacturing. All functions and roles of the manufacturing process are required to be performed with adherence to cGMP to ensure successful, quality operations. The candidate will also participate in cross-functional projects with Product Development (PD) and Process Engineering (PE) to develop, scale-up, and transfer new products. DUTIES AND RESPONSIBILITIES: Performs manufacturing activities according to cGMP guidelines, including batch record execution, product and equipment changeover, manufacturing equipment troubleshooting, issue resolution. etc. | 7/28/2020 |
| 10458 | ImmunityBio Louisville, CO Associate, Quality Control - Microbiology BS/BA in microbiology Exp: 1-3 year(s) |
The Associate, QC - Microbiology role will perform environmental monitoring, various testing, equipment troubleshooting/maintenance, and may assist with the drafting of SOPs, protocols, and reports to support manufacturing operations. Organizes daily workload and relevant resource requirements in an efficient manner. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in a fast-paced, highly interactive, goal-oriented team environment with minimal supervision. etc. | 7/28/2020 |
| 10459 | Amarin Chicago, IL Sales Professional- CHICAGO LOOP, IL BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the CHICAGO LOOP, IL territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 10460 | Amarin Tulsa, OK Sales Professional- TULSA, OK BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the TULSA, OK territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 10461 | Amarin Lee Summit, MO Sales Professional- KANSAS CITY E, MO BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the KANSAS CITY E, MO territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 10462 | Amarin Boise, ID Sales Professional- BOISE, ID BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the BOISE, ID territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 10463 | Amarin Tacoma, WA Sales Professional - TACOMA, WA BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the TACOMA, WA territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 10464 | Amarin Sarasota, FL Sales Professional- SARASOTA, FL BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the Sarasota, FL territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 10465 | Amarin Lima, OH Sales Professional-Lima, OH BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the Lima, OH territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 10466 | APi North Augusta, SC Quality Assurance Trainer BS/BA in biology, chemistry or other life science Exp: 1+ year(s) |
Major Responsibilities: Provide training to new employees on cGMP concepts, SOPs, Batch Record execution, Batch record reviews, and Investigations. Basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Review proposed SOP revisions and provide feedback to management. Real-time audit of batch records in the production suites for completeness, documentation, calculation errors and conformance to critical process parameters. etc. | 7/28/2020 |
| 10467 | APi North Augusta, SC Purification Chemist BS in chemistry or related Exp: Entry level |
Primary Responsibilities: Work in a cGMP environment to perform the peptide purification processes through chromatography as well as other various purification techniques. Use analytical skills to prevent and solve possible process complications and problems. Work as part of a team to complete specific projects in a timely manner. Follow approved cGMP manufacturing directions such as production batch records, standard operation procedures and standard test procedures. Help the team to install, test, operate and maintain equipment for manufacturing and in-process testing. etc. | 7/28/2020 |
| 10468 | APi North Augusta, SC MFG - Laboratory Technician HS diploma or equivalent Exp: Entry level |
Primary Responsibilities: Must manage and organize the glass cleaning operation according to approved standard operating procedures. Must manage time well. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. Follow approved GMP manufacturing directions such as standard operating procedures and other instructions in support of production. Responsible for documenting all production operations in logbooks and/or batch records. Perform the scheduled clean room cleaning activities as described by the standard operating procedure. etc. | 7/28/2020 |
| 10469 | APi North Augusta, SC QC Associate Microbiologist I or II BS in microbiology or other life sciences Exp: 1-5 year(s) |
Primary Responsibilities: Sampling and testing of city and pharmaceutical grade water per USP guidelines, SOP and Test method for bioburden, TOC, conductivity and endotoxin. Testing of product for release and stability for bioburden and endotoxin per USP guidelines, Test Method and SOP; endotoxin testing includes gel clot, chromogenic and turbidimetic. Bioburden testing includes method verification per USP <61>. Environmental monitoring sampling (viable and non-viable) per USP guidelines and SOP, as scheduled (daily, weekly, monthly, quarterly). Support production in qualification of clean rooms and water systems. Data entry for trending reports. etc. | 7/28/2020 |
| 10470 | APi North Augusta, SC MFG Cleaning Technician HS diploma or equivalent Exp: Entry level |
Perform scheduled cleaning of all water rooms. Perform scheduled cleaning of all Lyophilizer mechanical area. Help perform daily POU Flushes and twice a week POU Sanitizations. Perform any non-GMP cleaning as assigned. Must have good time management skills. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. Follow approved GMP manufacture directions such as standard operating procedures and other instructions for in support of production. Responsible for documenting all production operations and cleaning activities in logbooks and/or batch records. etc. | 7/28/2020 |
| 10471 | AmbryGenetics Aliso Viejo, CA QA Engineer I BS/BA in an engineering or computer related discipline Exp: 1+ year(s) |
The Quality Assurance (QA) Engineer for Bioinformatics is responsible to create and execute software test plans from the bioinformatics pipeline requirements, specifications and test strategies. The QA Engineer works with the bioinformatics team to define attainable testing goals and relay any issues from testing back to the team. Duties and Responsibilities: Create and execute software test plans for bioinformatics pipeline/software development process. Write test reports and communicate with technical and non-technical people. Identify, isolate, and track bugs throughout testing cycles and perform automated and manual testing and identify existing and potential issues. etc. | 7/28/2020 |
| 10472 | American Regent New Albany, OH Maintenance Technician - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
A technical position involving equipment repairs and maintenance activities intended to keep the facility equipment (i.e. process, utility, and general equipment) within compliance of cGMPs. Essential Duties and Responsibilities: Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Perform Preventative Maintenance Tasks: Follow written PM procedures. Accurately complete PM paperwork, including work orders and logbooks in accordance with existing company policies, procedures, and Current Good Manufacturing Practices, health and safety requirements. Perform PM of all types of plant equipment including coordinating access to equipment working around customer’s needs. etc. | 7/28/2020 |
| 10473 | Ampac Fine Chemicals Rancho Cordova, CA Operations Technician 1 HS diploma or equivalent Exp: 1-4 year(s) |
Operations Technician I will perform multiple duties related to the production of chemicals using a series if chemical processes in a batch type or continuous process chemical plant. These duties require careful observation and recording of data during all steps of the process. Little or no supervision required. Must have good technical and interpersonal skills to lead, direct, and instruct other employees. Some independent decision making will be required. May also be required to perform other duties in support of the plant activities not covered in another classification, including team participation. Assists in assigning tasks to other technicians, monitors performance of personnel, ensures that personnel follow all departmental and AFC policies and procedures, interacts with other personnel of other disciplines, participates in training fellow employees, conveys and logs status of processes, facilities, and personnel to the Crew Chief. etc. | 7/28/2020 |
| 10474 | Ampac Fine Chemicals Rancho Cordova, CA Quality Chemist I BS in chemistry or related Exp: 1-3 year(s) |
Duties: Perform analytical chemistry analyses in accordance with company SOPs and protocols following cGMP guidelines. Log-in samples. Work with potent chemical reagents and standards. Summarize data into reports. Ability to multi-task. Performs special projects as assigned. Test and analyze samples within the specified turn-a-round time. etc. | 7/28/2020 |
| 10475 | Amri Albany, NY Research Scientist I - Small Scale Manufacturing BS in organic chemistry Exp: Entry level |
Research Scientist I (Small Scale Manufacturing) in Albany, New York AMRI provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Research Scientist I (Small Scale Manufacturing) is an integral part of the AMRI team, contributing to our success by being part of a multi-disciplinary team, committed to the safe manufacture of active pharmaceutical ingredients (APIs) for use in human clinical trials. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. etc. | 7/28/2020 |
| 10476 | Amri Albany, NY Laboratory Technician - Analytical Development AS/BS in a science Exp: 1-2 year(s) |
In this role, you will: Conduct laboratory operations in a safe manner. Maintain familiarity with the Chemical Hygiene Plan. Exhibit safety awareness and safe work practices. Follow responsible actions regarding chemical disposal. Maintain compliance with all regulations at the federal, state, and local levels, as well as all appropriate SOP’s. Develop and maintain working knowledge of commonly used spectroscopic and physiochemical procedures. Analyze samples with the standard procedures effectively and under minimal supervision. Analyze experimental data for validity before reporting results. Keep contemporary, accurate, legible, and complete experimental records in accordance with GMP and GLP practices. etc. | 7/28/2020 |
| 10477 | Amri Springfield, MO Trainee, Chemical Operator HS diploma or equivalent Exp: Entry level |
In this role, you will: Safely manufacture fine chemicals. Intermediates and API manufacturing. Handle the various unit operations (reactions, filtration, distillation, drying, milling, etc.) that are performed on raw materials and various stages of chemical processing according to written manufacturing procedures and SOP’s. Follow and document per batch sheet instructions to produce product according to all cGMP guidelines. Ability to set-up equipment (vessels, tanks, centrifuges, dryers, etc.) for proper processing, Clean and verify equipment and vessels. Record observations of operating conditions. etc. | 7/28/2020 |
| 10478 | Amri Lebanon, NJ Quality Control Analyst I BS in engineering or related Exp: Not necessary for BS candidates |
In this role, you will; Assist with developing and validating test methods based on relevant ISO, ASTM standards and or client requirements. Independently perform tests per ISO, ASTM, and/or client requirements. Perform testing within the specified test plan and/or SOP for each test. Monitor projects for conformance with applicable SOPs and test specifications. Prepare test specimens for package/material/device testing. Manage multiple projects/tests at any one time ensuring all commitments are met. Collaborate with and train other laboratory staff on a project basis as appropriate. Document results and review data. etc. | 7/28/2020 |
| 10479 | Amri Springfield, MO Trainee, Chemical Operator HS diploma or equivalent Exp: Entry level |
In this role, you will: Safely manufacture fine chemicals intermediates and API manufacturing. Handle the various unit operations (reactions, filtration, distillation, drying, milling, etc.) that are performed on raw materials and various stages of chemical processing according to written manufacturing procedures and SOP’s. Follow and document per batch sheet instructions to produce product according to all cGMP guidelines. Ability to set-up equipment (vessels, tanks, centrifuges, dryers, etc.) for proper processing, Clean and verify equipment and vessels. Record observations of operating conditions. etc. | 7/28/2020 |
| 10480 | Amri Buffalo, NY Research Scientist I - Medicinal Chemistry BS/MS in chemistry or related Exp: 0-5 years |
Research Scientist I in Albany, NY AMRI provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Research Scientist I is an integral part of the AMRI team, contributing to our success by the synthesis, purification and identification of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. In this role, you will: Synthesize compounds efficiently using literature or in-house notebook procedures. Purify synthesized chemicals to an appropriate degree. The scientist will be able to use the full range of chromatographic, crystallization, and distillation techniques. etc. | 7/28/2020 |
| 10481 | Amri Albuquerque, NM Microbiologist I BS in a life science or related Exp: 0-2 years |
Albany Molecular Research Inc. provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. Summary: Prepare, collect, and test plant purified water, manufacturing raw materials, product in-process, and finished product, and perform environmental monitoring. With limited supervision, learn and perform critical laboratory techniques and complete original work. Author problem reports and participate in investigations. This description is inclusive of EM and testing duties: actual percentages of time spent on each duty may vary based on business needs. etc. | 7/28/2020 |
| 10482 | ARL BioPharma Oklahoma City, OK Sample Administrator I - Part Time HS diploma or equivalent Exp: 0-2 years |
Occupations that fit well with this position are pharmacy technician and medical office administrative assistant. The job is performed in an office environment. This position is to perform all data entry processes needed or required to facilitate the accurate reporting of all samples submitted for testing. The Accessioner maintains sample integrity to ensure accurate and timely testing and reporting by the appropriate lab. Additionally, the Accessioner may perform other duties requested by the Accessioning Supervisor. Minimal to moderate supervision is required. etc. | 7/28/2020 |
| 10483 | AngioDynamics Queensbury, NY Associate IT Service Desk Technician HS diploma or equivalent Exp: 0+ years |
Triage and resolve incidents, problems, and requests efficiently using our ITSM tool. Configure, install, and troubleshoot software, laptops, desktops, IP phones, mobile devices, printers, and other computer peripherals. Provide timely support onsite, remotely, and over the phone as part of our global IT call center. Perform after-hours work as needed on a rotating schedule. Procure standardized hardware and software from vendors, escalating non-standard requests to leadership. Follow change procedures for employee events (new hires, terminations, transfers, promotions, etc.). Assign roles and permissions to network resources such as SharePoint sites, file shares, and ERP systems. etc. | 7/28/2020 |
| 10484 | AMT Brecksville, OH Essential Detailed Device Assembly- 1st Shift HS diploma or equivalent Exp: 0-2 years |
Assembly of Percutaneous Endoscopic Gastrostomy (PEG) devices or products using like materials/components/assembly procedures. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Hand assembly and gluing of components. Use of manual and semiautomatic fixtures. Inspection of assembled components. Maintain quality and efficiency standards. Complete paperwork accurately and legibly. Cross-functional training required. etc. | 7/28/2020 |
| 10485 | AMT Brecksville, OH Essential Detailed Device Assembly- 2nd shift HS diploma or equivalent Exp: 0-2 years |
Assembly of Percutaneous Endoscopic Gastrostomy (PEG) devices or products using like materials/components/assembly procedures. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Hand assembly and gluing of components. Use of manual and semiautomatic fixtures. Inspection of assembled components. Maintain quality and efficiency standards. Complete paperwork accurately and legibly. Cross-functional training required. etc. | 7/28/2020 |
| 10486 | AMT Brecksville, OH Essential Entry Level Injection Molding Machine Operator-1st Shift HS diploma or equivalent Exp: Entry level |
Operates injection molding machines according to specific schedules and procedures. Prepares mold inserts and reviews molded component integrity. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Remove molded components from the mold once the machine has finished its cycle. Prepare cores and mold for next cycle. When applicable test parts during machine cycle to predetermined specifications. Inspect parts for overall integrity while machine is cycling. Maintain quality and efficiency standards. Use of manual and semiautomatic fixtures. Complete paperwork accurately and legibly. etc. | 7/28/2020 |
| 10487 | AMT Brecksville, OH Essential Entry Level Injection Molding Machine Operator-2nd Shift HS diploma or equivalent Exp: Entry level |
Operates injection molding machines according to specific schedules and procedures. Prepares mold inserts and reviews molded component integrity. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Remove molded components from the mold once the machine has finished its cycle. Prepare cores and mold for next cycle. When applicable test parts during machine cycle to predetermined specifications. Inspect parts for overall integrity while machine is cycling. Maintain quality and efficiency standards. Use of manual and semiautomatic fixtures. Complete paperwork accurately and legibly. etc. | 7/28/2020 |
| 10488 | AMT Brecksville, OH Essential Light Assembly Associate - 1st Shift HS diploma or equivalent Exp: Entry level |
Assembly of feeding sets and other basic assemblies or products using like materials/components/assembly procedures. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Visual inspection of devices, labels, and packaging. Use of manual and semiautomatic fixtures. Inspection of assembled components. Maintain quality and efficiency standards. Complete paperwork accurately and legibly. Cross-functional training required. etc. | 7/28/2020 |
| 10489 | AMT Brecksville, OH Essential Light Assembly Associate- 2nd Shift HS diploma or equivalent Exp: Entry level |
Assembly of feeding sets and other basic assemblies or products using like materials/components/assembly procedures. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Visual inspection of devices, labels, and packaging. Use of manual and semiautomatic fixtures. Inspection of assembled components. Maintain quality and efficiency standards. Complete paperwork accurately and legibly. Cross-functional training required. etc. | 7/28/2020 |
| 10490 | AMT Brecksville, OH Essential Molding Machine Operator- 3rd Shift HS diploma or equivalent Exp: Entry level |
Operates injection molding machines according to specific schedules and procedures. Prepares mold inserts and reviews molded component integrity. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Remove molded components from the mold once the machine has finished its cycle. Prepare cores and mold for next cycle. When applicable test parts during machine cycle to predetermined specifications. etc. | 7/28/2020 |
| 10491 | Archer Boulder, CO Quality Control Associate BS Exp: 1-3 year(s) |
Job performance will involve a variety of activities including: Execution of work instructions for testing raw materials, in-process materials/sub-assemblies, and top-level IVD materials to determine compliance to specifications. Critical analysis of data ensuring compliance with standards and specifications. Generation of data reports. Adherence to safety and quality laboratory standards. Upkeep of personal training and associated records. Maintenance of laboratory material stocks and initiation of re-orders. Execution of method validation and stability testing protocols. Identification of non-conforming material and subsequent report initiation and generation (OOS/OOT investigation). etc. | 7/28/2020 |
| 10492 | Argon Medical Devices Athens, TX Manufacturing Engineer I BS in mechanical or industrial engineering Exp: 1-2 year(s) |
The Manufacturing Engineer will be responsible for leading and participating in creating, finding, and evaluating better and more efficient ways to manufacture products and provide ongoing production support for Argon Medical products and manufacturing sites. The Manufacturing Engineer will work to manage and communicate progress towards project goals to management effectively. The Manufacturing Engineer will work to gather and document customer requirements, translate them into measurable product requirements, and provide engineering support for the development and manufacture of Argon Medical Device products. etc. | 7/28/2020 |
| 10493 | Argonaut Manufacturing Services Carlsbad, CA Technical Transfer Operator, Drug Product Manufacturing BS in a life science or engineering Exp: 1-3 year(s) |
The purpose of this position is to transfer product and process knowledge from developmental clinical production to GMP product manufacturing in the drug product manufacturing division of Argonaut. Responsibilities: Facilitate transfer of new processes from client lab or concept to drug product manufacturing by collaborating with subject matter experts and operations management. Participate in client discussions via phone, video conference, and/or onsite visits. Create and revise client-specific batch records, raw material specifications, and any documentation related to Drug Product Manufacturing. Review executed batch records and other documentation, as needed. etc. | 7/28/2020 |
| 10494 | Arthrex Ave Maria, FL Laser Machine Operator I- Second Shift HS diploma or equivalent Exp: 6+ months |
Main Objective: To produce superior products following Arthrex Manufacturing Inc. machining processes and procedures. This position is eligible for a sign-on bonus. If you are hired, you will be eligible for a $750.00 sign-on bonus (minus appropriate tax withholdings) paid after you complete your first 90 days and are an employee in good standing. Essential Duties and Responsibilities: Operation of Assembly, Laser Mark, Laser Weld, and EDM equipment in accordance to work instructions. Inspect machined work piece to specifications, based on correct AQL. Verify inspection tools issued to job are available and correct. Receives and verifies work order and verifies that the components are correct. Notifies Supervisor or Lead if equipment is not operating properly. etc. | 7/28/2020 |
| 10495 | Arthrex Ave Maria, FL Textile Technician - 2nd Shift HS diploma or equivalent Exp: 1 year |
Arthrex Manufacturing is hiring additional team members to the Textile department on second shift. The Textile Technician is responsible for setting and operating machines that produce the materials for the Sutures department. The second shift hours are 4:00 pm to 12:30 am, Monday through Friday. Training will be on first shift for approximately 8 weeks. The job location will be at the Arthrex manufacturing facility in Ave Maria, FL. Essential Duties and Responsibilities: Set-up and operate a variety of hand tools and light duty textile machines to manufacture product specified on work order using engineering prints, standard work instructions and Inspection procedures. Manufacture the finished product to specifications with the use of measuring equipment, specialized hand tools and microscopes, making decisions in equipment setup parameters within established guidelines to achieve the required specifications. etc. | 7/28/2020 |
| 10496 | Accelerate Diagnostics Tucson, AZ Research Associate, Quality Control BS in chemistry, microbiology, biochemistry, molecular biology, or related Exp: 1+ year(s) |
The Research Associate for Quality Control is a key member of the Operations Team under the direction of the Team Lead for Consumable Quality Control. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, HPLC-MS, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. etc. | 7/22/2020 |
| 10497 | Accuray Madison, WI Microwave Technician/CNC Welder AS in production, manufacturing or general engineering Exp: Not necessary for AS candidates |
The Technician is responsible for the re-manufacture and repair activities of linear accelerators (linacs) that allow Accuray to provide products that meet customer needs and do so in accordance with regulatory requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES: Performs CNC machining operations in the Linac Repair Center. Performs precision Tungsten Inert Gas (TIG) welding of copper, Kovar, and stainless steel. Investigates field returns to decide what the failure was and what actions need to be taken for repair. Assembles and disassembles linear accelerators in accordance with schedule and in accordance with quality system requirements, procedures, and work instructions. Uses Rf equipment for tuning of linear accelerators. etc. | 7/22/2020 |
| 10498 | Acell Columbia, MD Biotechnician HS diploma or equivalent Exp: Entry level |
This is an entry level position for a Biotechnician. Employee will carry out manufacturing practices in a cGMP biotechnical facility. The job involves the manual processing of porcine urinary bladders, which includes all aspects from collection of raw materials to packaging of the final product. Following training, work will be expected to be performed independently to a high degree of standard in biomaterial handling. Principal Responsibilities: Collection of raw materials. Rinse and initial cleaning of raw materials upon receipt. Separation and removal of unwanted tissues. Disinfection. Preparation of storage and cleaning solutions. etc. | 7/22/2020 |
| 10499 | Acell Lafayette, IN Biotechnician - Second Shift HS diploma or equivalent Exp: Entry level |
This is an entry level position for a Biotechnician. Employee will carry out manufacturing practices in a cGMP biotechnical facility. The job involves the manual processing of porcine urinary bladders, which includes all aspects from collection of raw materials to packaging of the final product. Following training, work will be expected to be performed independently to a high degree of standard in biomaterial handling. Principal Responsibilities: Collection of raw materials. Rinse and initial cleaning of raw materials upon receipt. Separation and removal of unwanted tissues. Disinfection. Preparation of storage and cleaning solutions. etc. | 7/22/2020 |
| 10500 | Acella Pharmaceuticals Dallas, TX Pharmaceutical Sales Representative (NP) BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. Responsible for providing healthcare providers with all relevant information that promotes quality healthcare decisions. Employ effective selling techniques, including pre-call planning, effective opening, presentation focus, productive questions, issues identification and effective close. etc. | 7/22/2020 |
| 10501 | Acumed Wichita, KS Sales Associate, Wichita, Kansas - Future Opportunities BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. Continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 7/22/2020 |
| 10502 | Acumed Hillsboro, OR Quality Engineer I BS in engineering or a science Exp: 1-3 year(s) |
The Quality Engineer is responsible for providing Quality Assurance support to product development and manufacturing to increase product quality, reliability, and process capability. Responsible for identifying, documenting, assessing, correcting and presenting quality issues using risk and root cause analysis tools. Supports quality of new products being released to the market through participation in the product development process to ensure product and process conformance to global standards (including FDA and ISO 13485). Serves as a quality representative to design control, verification and validation, design transfer, and risk management on assigned product development teams ensuring compliance with Acumed policies and global regulations, including FDA Quality System Regulation and ISO 13485. etc. | 7/22/2020 |
| 10503 | Acumed Kansas City, KS Associate Sales Representative - Kansas City, KS BS in engineering or a science Exp: 0-2 years |
The Associate Sales Representative (ASR) exceeds sales quota within an assigned territory by delivering Acumed product on time and providing high quality technical assistance in the OR. The ASR assists in the assessment of the customer base to identify new business opportunities and executes a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. Duties/Responsibilities: Execute business plans to identify and close new business. Identifies the needs of new prospects and develops/delivers appropriate responses to meet or exceed needs (written, telephone and face-to-face). etc. | 7/22/2020 |
| 10504 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I - PCR/Sequencing (Sun-Wed PM) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
The Clinical Laboratory Technologist 1 position will be responsible for processing medically relevant biological samples through extraction or high throughput DNA sequencing assays. This role will work within a team of Laboratorians in a fast-paced, high production setting to process research and clinical diagnostic samples to provide a test result to patients, oncologists and other medical practitioners and researchers. As such, high attention to detail and clinical mindedness are crucial to success in this role. Responsibilities: Assignment to one of two labs performing either DNA extractions from human biological samples, or PCR amplification and high-throughput sequencing assays on DNA libraries. Demonstrate good clinical judgment and integrity. Perform DNA extractions, PCR amplification or high-throughput sequencing assays on DNA libraries. etc. | 7/22/2020 |
| 10505 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I - PCR/Sequencing (Sun-Wed AM) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
The Clinical Laboratory Technologist 1 position will be responsible for processing medically relevant biological samples through extraction or high throughput DNA sequencing assays. This role will work within a team of Laboratorians in a fast-paced, high production setting to process research and clinical diagnostic samples to provide a test result to patients, oncologists and other medical practitioners and researchers. As such, high attention to detail and clinical mindedness are crucial to success in this role. Responsibilities: Assignment to one of two labs performing either DNA extractions from human biological samples, or PCR amplification and high-throughput sequencing assays on DNA libraries. Demonstrate good clinical judgment and integrity. Perform DNA extractions, PCR amplification or high-throughput sequencing assays on DNA libraries. etc. | 7/22/2020 |
| 10506 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I - Extraction (Thurs-Sat PM) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
The Clinical Laboratory Technologist 1 position will be responsible for processing medically relevant biological samples through extraction or high throughput DNA sequencing assays. This role will work within a team of Laboratorians in a fast-paced, high production setting to process research and clinical diagnostic samples to provide a test result to patients, oncologists and other medical practitioners and researchers. As such, high attention to detail and clinical mindedness are crucial to success in this role. Responsibilities: Assignment to one of two labs performing either DNA extractions from human biological samples, or PCR amplification and high-throughput sequencing assays on DNA libraries. Demonstrate good clinical judgment and integrity. Perform DNA extractions, PCR amplification or high-throughput sequencing assays on DNA libraries. etc. | 7/22/2020 |
| 10507 | Adare Pharmaceuticals Vandalia, OH Document Control Specialist I BS/BA Exp: Not necessary for BS/BA candidates |
Responsible for conducting day to day quality documentation processing for cGMP documents, and provide support to internal end users on document management processes. ESSENTIAL DUTIES AND RESPONSIBILITIES: The primary duties and responsibilities of this position include the following. Other duties may be assigned. Formats, tracks and issues controlled cGMP documents. Assist in review of cGMP controlled documents as necessary. Issuance of batch production records, tracking of master batch records, and tracking of all batch production records. Supports quality audits (internal and external), troubleshooting efforts, and other Quality System processes. Evaluates issues received from end users and makes decision on appropriate follow-up steps. Scan, image, organize and maintain documents, adhering to the company's document lifecycle procedures, and they archive inactive records in accordance with the records retention schedule. Maintains filing of all master documents. Maintains an efficient and easily retrievable documentation system for all the documents. etc. | 7/22/2020 |
| 10508 | Adare Pharmaceuticals Vandalia, OH Analytical Scientist I BS/MS in chemistry or the physical sciences Exp: Entry level |
The essential job function is to support the development and validation of analytical methods for raw materials, work-in-process, and finished products and to provide testing support for the formulation development and clinical supplies release process. ESSENTIAL DUTIES AND RESPONSIBILITIES: The primary duties and responsibilities of this position include the following. Other duties may be assigned. With supervision and direction the analyst is required to: Provide support for the development and validation of pharmaceutical analytical methods for potency, dissolution, impurities/degradation products, residual solvents…using appropriate laboratory instrumentation e.g. HPLC, UHPLC, LC-MS, Dissolution Apparatus, GC… etc. | 7/22/2020 |
| 10509 | Admera Health South Plainfield, NJ Associate Scientist I/II-Lab BS/MS in biological sciences Exp: 1-3 year(s) |
Responsibilities: Preparing solutions and reagents for performing assays on the bench. Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): RNAseq, Whole Genome Sequencing, Whole Exome Sequencing. Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. Strict record keeping of all laboratory procedures. etc. | 7/22/2020 |
| 10510 | ABL Rockville, MD QC Microbiologist I BA/BS in microbiology, biology, or related Exp: 1-2 year(s) |
The QC Analyst Microbiology will have several responsibilities in the QC group. The analyst will perform environmental monitoring (EM) for particulates and viables in support of cGMP manufacturing which includes several production suites of ISO class 5, 7, and 8 as well as EU Grade A to D in a GMP facility that produces biopharmaceuticals (vaccines, biologics, viral vaccines, monoclonal antibodies, etc.). In addition, monitoring of purified water, and compressed gases systems is required. Additional responsibilities may include EM data review and compilation of data, report writing, and trending of data; investigations, gowning training and annual gowning qualification. etc. | 7/22/2020 |
| 10511 | Advanced Vision Sciences Goleta, CA Bookkeeper AS/AA Exp: Not necessary for AS/AA candidates |
This position is responsible for the timely and accurate processing of payroll and maintaining payroll records; timely and accurate processing and payment of Accounts Payable and maintaining AP records; timely and accurate processing of General Ledger journal entries and Balance Sheet account reconciliations; Assist in month end close process. MAJOR DUTIES OF POSITION: Process biweekly payroll and maintain all payroll records. Prepare periodic reports of earnings, taxes and deductions. Keep record of leave pay (sick, vacations, disability). Prepare and transmits 401K spreadsheets. Prepare and uploads 125K spreadsheets. etc. | 7/22/2020 |
| 10512 | B. Braun Allentown, PA IV Tech I HS diploma or equivalent Exp: 1+ year(s) |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Responsibilities: Essential Duties: Prepares compounded sterile products using aseptic technique. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. Participates in cleanroom product introduction activities. Prepares records and monitors results for pharmaceutical quality assurance testing. etc. | 7/22/2020 |
| 10513 | B. Braun Phoenix, AZ Pharmacy IV Technician HS diploma or equivalent Exp: 1+ year(s) |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Responsibilities: Essential Duties: Prepares compounded sterile products using aseptic technique. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. Participates in cleanroom product introduction activities. Prepares records and monitors results for pharmaceutical quality assurance testing. etc. | 7/22/2020 |
| 10514 | B. Braun Irvine, CA PMO Analyst I BS/BA Exp: 0-2 years |
Responsibilities: Essential Duties: Under the direction of the PMO Manager, supports the Project Management Office (PMO) related activities to ensure the success of the PMO and its objectives. Works collaboratively in a team environment (Corporate, Manufacturing, Quality, Operations, Supply Chain, Procurement, Engineering, etc.) in support of PMO activities. Collaborates with Project Leaders to update and manage the project portfolio data and capital spend and forecast data via spreadsheet and the project portfolio management system (PPMS). Supports the creation and maintenance of key project portfolio metrics using Excel, Powerpoint, and other tools to provide visibility to management. etc. | 7/22/2020 |
| 10515 | B. Braun Irvine, CA Product Handler (Excel Filling Pooling) HS diploma or equivalent Exp: 0-4 years |
Responsibilities: Essential Duties: Assists supervisor to ensure that production operators have sufficient stock of materials. Collects, checks and keeps records of materials flow to and from production area. Etc. | 7/22/2020 |
| 10516 | Ajinomoto Bio-Pharma Services San Diego, CA Temporary Drug Product Support Technician HS diploma Exp: 0-1 year(s) |
We are currently seeking multiple Temporary Drug Product Support Technicians to join the team. In this role you will be responsible for packing and labeling and offload activities for our various drug products. Responsibilities: Operates filled drug product offloading equipment. Accurate receipt and counting of filled units from Fill Finish manufacturing. Responsible for product transfers to Materials Management. Responsible for assisting with pre and post Line Clearance, and Good Documentation Practices (GDP). H24Perform Bulk Packaging and Labeling of Vials or Syringes. Follow all proper gowning procedures. etc. | 7/22/2020 |
| 10517 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Assistant HS diploma/BS in a life science Exp: 0-2 years |
We are looking for multiple Drug Product Manufacturing Assistants for 1st Shift! The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. Responsibilities: Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Implements production and manufacturing procedures. Performs visual inspection. Prepares components, media, buffers, and other solutions as needed. Accurately documents data and completes batch records as needed. May cross train and/or focus in various manufacturing tasks including fill/finish, formulation, fermentation, preparation. Operates production equipment and may prepare buffers and media, inspect, label, or box. etc. | 7/22/2020 |
| 10518 | Agilent Santa Clara, CA Business Process Associate BS/BA/MS/MA Exp: 1+ year(s) |
The Business Process Associate role reports into the Global Sales Enablement (GSE) team, which supports LSS Global Sales and Marketing functions. This team collaborates cross-functionally with sales, marketing, service, SUs and other supporting organizations, to effectively execute strategic LSS and Corporate programs across the world. We're looking for a talented and motivated professional to join the team. Responsibilities include: Responsible for analysis and evaluation of user business problems and development of business system or process recommendations to meet requirements, including problem definition, evaluation of requirements, and implementation of systems/processes. etc. | 7/22/2020 |
| 10519 | Akorn Amityville, NY Metrologist AS/AA in instrumentation engineering Exp: Not necessary for AS/AA candidates |
The Calibration Technician is responsible for the following activities: Ability to perform all Calibration Technician I functions. Ability to work independently installing, troubleshooting, and calibrating all types of instruments or control systems in any Akorn environment. Maintain calibration records and enter calibration data using software such as Calibration Manager. Daily review and update the calibration validation data. Fluently use software such as MS Excel, Word, and other maintenance manager software such as AMMS to purchase items and complete validation documentation. Develop SOPs for new or existing equipment as required. Coordinate equipment calibrations for equipment to be calibrated. etc. | 7/22/2020 |
| 10520 | Akorn Somerset, NJ Production Line Operator (3 pm - 11:30 pm) HS diploma or equivalent Exp: 1 year |
All Production Line Operators are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. ESSENTIAL FUNCTIONS: Include the following. Other duties may be assigned. Compliance with associated SOPs and training requirements. Basic understanding of personnel, equipment flow and controlled environments. Prepare for aseptic gowning qualifications. NOTE: Must have flexibility, discipline and not fall out of established limits. Basic understanding of aseptic procedures and cleanroom behavior in controlled environments. Transport sterile components and supplies from a controlled 10000 classification environment to a 1,000 classification environment and from 1,000 classification environment to 100 classification environment. Observation and processing of fills/rooms in #1 and #2 areas. etc. | 7/22/2020 |
| 10521 | Akorn Decatur, IL 2nd shift Production Technician – Lead HS diploma or equivalent Exp: Not necessary |
Direct oversight of assigned production fill room, equipment preparation or glassware preparation employees. Carries out leadership responsibilities in accordance with the organization’s policies and applicable laws. Responsibilities include training employees; planning, assigning, and directing work; appraising performance; addressing complaints and resolving problems. Must be able to communicate effectively with all levels of employees. Must be able to perform simple math calculations. Must be able to solve problems, handle conflict, and make effective decisions under pressure. ESSENTIAL LEAD TECHNICIAN DUTIES AND RESPONSIBILITIES: Include the following. Other duties may be assigned. Provide oversight of the Key Process Steps; i.e., equipment set up and alignment, defined line speed, hold times, machine prime, etc. In addition: Media fill completed in strict adherence to the Batch Record and Media SOP requirements. etc. | 7/22/2020 |
| 10522 | Akorn Somerset, NJ Production Line Operator (2nd Shift - 6 pm - 2:30 am) HS diploma or equivalent Exp: 1 year |
All Production Line Operators are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. ESSENTIAL FUNCTIONS: Include the following. Other duties may be assigned. Compliance with associated SOPs and training requirements. Basic understanding of personnel, equipment flow and controlled environments. Prepare for aseptic gowning qualifications. NOTE: Must have flexibility, discipline and not fall out of established limits. Basic understanding of aseptic procedures and cleanroom behavior in controlled environments. Transport sterile components and supplies from a controlled 10000 classification environment to a 1,000 classification environment and from 1,000 classification environment to 100 classification environment. Observation and processing of fills/rooms in #1 and #2 areas. etc. | 7/22/2020 |
| 10523 | Akorn Decatur, IL 2nd shift Environmental Monitoring Technician HS diploma or equivalent Exp: 1 year |
The Environmental Monitoring Technician I will perform all environmental monitoring tests required to monitor the manufacturing controlled areas at Akorn’s Grand Avenue facility. ESSENTIAL FUNCTIONS: Include the following. Other duties may be assigned. Must be able to demonstrate and apply good aseptic technique and cleanroom behavior. Must be able to demonstrate and apply good gowning technique during certification, re-certification, and routine monitoring. Must be able to understand the operation and application of all monitoring devices that are automated or manual operation in the department. Must be able to demonstrate the ability to monitor and document all environmental parameters, such as viable sampling, personnel sampling, temperatures, humidity, and differential pressures under static and dynamic conditions. Fill out cleanroom information sheets. etc. | 7/22/2020 |
| 10524 | Alcami Charleston, SC Environmental Monitoring Tech I- 3rd Shift BS/BA Exp: 0-2 years |
The Environmental Monitoring Technician I is accountable for results in a fast-paced environment. The Level I Technician follows applicable SOPs and cGMPs to perform environmental monitoring for the facility, and may also perform simple, routine basic interpretation of environmental monitoring (EM) results, typically under supervision. This position is also responsible for hazardous waste and sanitation/cleaning of the Microbiology laboratory. The position requires strong leadership behaviors of the Alcami core competencies and non-negotiables, as well as the functional competencies of this profile. Essential Functions: Performs routine daily, weekly and monthly sampling of Water for Injection, compressed gas and the environment to detect microbial, non-viable and chemical contamination. Supports manufacturing operations by continuous environmental monitoring viable and non-viable particles. etc. | 7/22/2020 |
| 10525 | Alcami Germantown, WI Regulatory Affairs Specialist I BS/MS in science or engineering Exp: 1+ year(s) |
The Regulatory Affairs Specialist is accountable for driving results in a fast-paced environment by performing activities to ensure that regulatory submissions support active pharmaceutical ingredient (API) business needs and that the business remains compliant with regulatory filings. Activities include preparation and submission of regulatory filings, written and verbal communication with regulatory agencies and clients, and providing regulatory affairs information and counsel to other site functions. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. Essential Functions: Remain informed about regulations and regulatory trends concerning US FDA and other countries’ regulatory agencies. etc. | 7/22/2020 |
| 10526 | Alcami Charleston, SC Manufacturing Tech- 3rd Shift HS diploma/AS/AA Exp: 0-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. etc. | 7/22/2020 |
| 10527 | Alcami Morrisville, NC Manufacturing Tech I HS diploma/AS/AA Exp: 0-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. etc. | 7/22/2020 |
| 10528 | Alcami Charleston, SC Manufacturing Tech- Weekend Shift HS diploma/AS/AA Exp: 0-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. etc. | 7/22/2020 |
| 10529 | Alcami Charleston, SC Material Control Tech I HS diploma/AS/AA Exp: 0-2 years |
The Materials Control Technician I is accountable for results in a fast-paced environment by following applicable SOPs and cGMPs to perform tasks for the receipt, storage, inventory and distribution of raw materials, intermediate or finished drugs or drug products and components. The Materials Control Technician I uses the electronic inventory system to track, document and control all inventory. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. etc. | 7/22/2020 |
| 10530 | Alkermes Wilmington, OH Training Technology Specialist I BS in information technology Exp: 1-3 year(s) |
This position supports the Operations Training Group in use of technology software, hardware, applications, video, etc.… for training development and delivery. Supports the development of content for the departmental training materials for Good Manufacturing Practices (GMP) training. Provides basic information technology training classes and training resources to departmental areas of responsibility. Provides training information technology guidance to area trainers and maintains/updates the departmental Sharepoint site. This position supports a comprehensive operations training strategy that aligns to the departmental talent strategies and supports the overall organizational strategy. etc. | 7/22/2020 |
| 10531 | Alkermes Wilmington, OH QC Analyst II - Micro BS in biology, microbiology, biotechnology, biochemistry Exp: 1 year |
QC Analyst Il must have broad knowledge of all the techniques within the laboratory required for the routine support of the microbiology laboratory operations. In this role the Analyst will be a fully functional member of the team responsible for testing, data entry and occasional review of data for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment. Major Responsibilities: Execution of microbiological tests including but not limited to bioburden, LAL, growth promotion, sterility, particulate profiling and microbial identification of bulk, raw materials, in-process material, components, clinical materials and finished product. If required, must be able to perform cGMP biological testing (bioassays, flow cytometry, qPCR, and ELISA). Review and data entry for testing results following GMP regulations into the electronic data management systems. etc. | 7/22/2020 |
| 10532 | Alkermes Wilmington, OH QA Associate I/II BS Exp: 1-2 year(s) |
This function is responsible for supporting the daily on the floor activities related the manufacturing operations and quality systems. Functions include on the floor batch record review, discrepancy identification, logbook review, status tagging, room/utility checklists, document control and product shipping. This function thresholds events to Senior Associate when they are outside of the area of responsibility. The position will perform general QA work, using their ability as a skilled contributor in completing tasks where judgement is required in resolving problems and making recommendations. Works on problems of a diverse scope where analysis and problem solving is required. Receives general oversight and guidance on approaches to complete project related tasks. Applies job related skills and understanding of policies and standards in completing tasks. etc. | 7/22/2020 |
| 10533 | B. Braun Irvine, CA Machine Attd (Titan Filling) HS diploma or equivalent Exp: 1-5 year(s) |
Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organization's products according to production specifications and schedules, volume, cost, and wastage targets or quality standards. Operates machines and production equipment safely and in accordance with instructions. Monitors the quality of output to identify, discard or remanufacture faulty products. Maintains accurate daily production records so that manufacturing performance can be analyzed. Troubleshoots and resolves technical problems from the product line/process to minimize reject levels.-For more senior position, might act as a team leader to ensure that the work meets agreed targets by directly overseeing team members. etc. | 7/22/2020 |
| 10534 | B. Braun unspecified, US Sales Associate BS/BA Exp: 0-4 years |
The Sales Associate Program is a full time, entry-level development program designed to serve as an entry point to a career in Sales at B. Braun Medical Inc. We will provide rigorous, comprehensive, hands on training for up to 24 months. At the conclusion of the program, participants will have the opportunity to be placed in a Sales role in a dedicated geography. Program participants will have exposure to the many different elements of Sales, while learning B. Braun's processes to achieve success. There are endless opportunities to build networks, develop strong relationships, and gain credible work experience. This program enables growth and development across the Sales organization, with structured mentoring from senior account managers. etc. | 7/22/2020 |
| 10535 | B. Braun Hazelwood, MO Technician, Endoscopic HS diploma Exp: 6 months |
Summary: Responsible for repairing, refurbishing and cleaning of basic precision Endoscopic/Laparoscopic surgical instruments under supervision of lead. Principal Duties Responsibilities: Buffs, Polishes, grinds, and performs minor repairs on basic surgical instruments. Instruments include but are not limited to Aesculap Endoscopic/Laparoscopic instruments. Surface treatment. Red-wheeling and bead blasting as needed. Repair, replace, realign to complete full refurbishment of basic instrumentation. etc. | 7/22/2020 |
| 10536 | FYR Diagnostics Missoula, MT Lab Technician BS or MS in biological sciences Exp: 0-2 years in lab |
Learn laboratory-based skills and work with an interdisciplinary team investigating novel isothermal PCR-based technology. Work with other researchers and technicians to execute, analyze and interpret PCR-focused experiments and miscellaneous in vitro experiments. Preparation of reagents and samples for experiments | 7/18/2020 |
| 10537 | Fzata Halethrope, MD Administrative Assistant BS/BA Exp: 1 y ear as admin assistant |
Prepare documents, reports for managers. Schedule and coordinate meetings, travel arrangement. Data processing, input and verification. Monitor and track expenses | 7/18/2020 |
| 10538 | Cosette Pharmaceuticals Lincolnton, NC QC Auditor I (TEMP) BS or BA in chemistry Exp: 1 year in labaa auditing documentation |
The purpose of this position is to review QA/QC documentation, to assess data compliance/validity with regulatory guidelines in the Quality Control Department and ensure that all the work is performed and documented accurately, timely and in compliance with internal procedures and regulatory agencies. Provide technical support for the release of raw materials, finished products, and stability data. | 7/18/2020 |
| 10539 | Cosette Pharmaceuticals South Plainfield, NJ MANUFACTURING OPERATOR 1 HS Diploma or GED Exp: 1-2 years in cGMP |
Perform work within the manufacturing department to clean equipment/rooms, dispense, and operate equipment for product studies, development, and commercial production. | 7/18/2020 |
| 10540 | GenapSys Redwood City, CA Research Associate, Systems Integration MS in biological sciences or engineering Exp: 0-2 years in lab |
Participate in development and optimization of NGS Platform workflow steps, in order to improve the existing performance of our NGS platform. Participate in short-term and long-term exploratory studies of assay development on Genapsys platforms. Plan and execute experiments, perform in-depth data analysis and present results and conclusions for internal review, and evaluate the research of peers. | 7/18/2020 |
| 10541 | GeneDx Gaithersburg, MD Medical Lab Technologist BS in med technology, biology, or chemistry Exp: 1 year in CLIA lab |
The Medical Lab Technologist performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Maintain standards in routine & STAT testing. Complete work in a timely manner. Write legibly when documenting QC, problems or information. | 7/18/2020 |
| 10542 | GeneDx Gaithersburg, MD DNA Extraction Technician BS in medical technology or life sciences Exp: 0-1 years |
Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed | 7/18/2020 |
| 10543 | GeneDx Gaithersburg, MD Lab Technician, Microarray BS in medical technology or life sciences Exp: 1 year in technologies |
The Laboratory Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease, using manual and automated methods in a team environment, and following established policies and procedures in a professional manner.Implements the standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. | 7/18/2020 |
| 10544 | Generation Bio Cambridge, MA Associate Scientist InVivo Care and Resources HS Diploma/GED or BS Exp: 1-3 years in lab animal husbandry |
Perform daily husbandry of rats and mice under modified barrier conditions and document accordingly. Monitor and document animal facility conditions including temperature and humidity daily. Perform twice daily health monitoring of animals, document and report abnormal conditions to the supervisor. Perform general upkeep and cleaning of facility including daily sweeping and mopping and quarterly cleaning | 7/18/2020 |
| 10545 | Generation Bio Cambridge, MA Associate Scientist / Senior Associate Scientist, Drug Product Formulation-CMC MS in pharmacuetics, chemical sciences/engineering Exp: 0-2 years |
Execute on development work for the manufacturing processes for Drug Product formulation using both DNA vectors and Lipid Nanoparticles (LNPs). Ensures all appropriate materials, equipment, protocols and documentation are available and completed for multiple Drug Product formulations targeted for research and pre-clinical programs. | 7/18/2020 |
| 10546 | Genewiz South Plainfield, NJ Associate Scientist I BS/BA in biological sciences Exp: 1+ year in biological laab |
Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. Communicate with customers by phone and e-mail in a friendly and professional manner | 7/18/2020 |
| 10547 | Neo Genomics Carlsbad, CA Logistics Technician HS Diploma/GED Exp: 1 year as accessioning technician |
The Logistics Technician will ensure proper handling of all specimens received and prepare specimens for laboratory testing. This position includes such functions as matching patient information, data entry, and scanning documents. This is entry level in the Logistics job category, and employees perform the full range of specimen processing procedures. | 7/18/2020 |
| 10548 | Neo Genomics Aliso Viejo, CA Clinical Laboratory Technologist, Molecular BS/BA in biological/chemical sciences Exp: 1+ years in clinical lab work |
In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations.Maintains laboratory in a clean, functional state, as well as cleaning, performing or scheduling equipment and instrument maintenance/calibration/certification, as required | 7/18/2020 |
| 10549 | Ginkgo Bioworks Boston, MA Production Operations Engineer Assocites in computer science, engineering or related Exp: 1 year in network/production support |
Provide front-end support for our high-complexity CLIA laboratory. Establish root causes of application errors, escalating serious concerns to engineering team members and ensuring issue resolution. Actively participate in post mortem discussions. Manage detailed records of configuration changes | 7/18/2020 |
| 10550 | Ginkgo Bioworks Boston, MA High-Throughput Screening Research Associate BS or MS in biological/chemical sciences or engineering Exp: 1-3 years research experience |
We’re looking for highly talented and motivated research associates to join our high-throughput screening (HTS) team and help carry out these critical functions. High-throughput culturing of microbial strains using a variety of automated solutions for use in high-throughput screens. Creation of strain libraries through the execution of a HTP transformation and colony picking workflows. | 7/18/2020 |
| 10551 | Ginkgo Bioworks Boston, MA Foundry Operations Engineer - Fermentation BS/BA Exp: 1+ year industry experience |
Execute fermentation processes across multiple Ginkgo organisms, with a focus on filamentous fungi, bacteria, and yeast as directed by senior engineers. Maintain responsibility for setup and breakdown of fermentation equipment. Aid in the preparation of media and other required reagents. Collect and process samples | 7/18/2020 |
| 10552 | Ginkgo Bioworks Boston, MA Build Engineer / Research Associate BS or MS in microbiology or genetics Exp: 1+ year in lab |
We are seeking inquisitive research associates to join our Build team to help us run and improve several high-throughput molecular biological processes. A demonstrated ability to evolve a process in response to changing technology and demands is essential. Experience in a mixed team of software developers, process engineers, and biologists is important. | 7/18/2020 |
| 10553 | GenapSys Redwood City, CA Research Associate, Development MS in molecular biology Exp: 1+ year in industry |
Help to define technical requirements for consumable products and generate data to support the specifications that are established and used for incoming QC. Participate on both short-term and long-term stability studies to establish high risk reagents, work flow and storage issues. Help to develop orthogonal analytical methods that can correlate with performance on our sequencing platform. | 7/18/2020 |
| 10554 | Genewiz Cambridge, MA Laboratory Technician I HS Diploma/GED Exp: 1+ year in lab |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 7/18/2020 |
| 10555 | Genewiz South Plainfield, NJ Associate Scientist I BS in biological sciences Exp: 1+ year in biological laab |
Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. Communicate with customers by phone and e-mail in a friendly and professional manner | 7/18/2020 |
| 10556 | Genewiz La Jolla, CA Laboratory Technician I HS Diploma/GED Exp: 1+ year in lab |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 7/18/2020 |
| 10557 | Neo Genomics Carlsbad, CA Laboratory Technician - Covid-19 Unit BS/BA in life sciences or engineering Exp: 0-2 years |
As a Laboratory Technician you will work under the direct supervision of licensed personnel to prepair Covid-19 samples for processing. You will assist with responsibilities associated with processing specimens for clinical testing and will provide general support for the laboratory following established policies and procedures. | 7/18/2020 |
| 10558 | Neo Genomics Ft. Myers, FL Clinical Laboratory Technologist I - Molecular- Tuesday -Saturday; Day Shift BS/BA in biological/chemical sciences Exp: 1+ year in clinical lab |
In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 7/18/2020 |
| 10559 | Neo Genomics Carlsbad, CA Clinical Laboratory Technologist -Covid-19 Testing Unit BS/BA in biological/chemical sciences Exp: 1+ year in clinical lab |
In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 7/18/2020 |
| 10560 | Neo Genomics Carlsbad, CA Clinical Laboratory Technologist - Covid-19 Unit BS/BA in biological/chemical sciences Exp: 1+ year in clinical lab |
In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications | 7/18/2020 |
| 10561 | Ginkgo Bioworks Boston, MA Research Associate, Protein Engineering BS or MS in biological sciences or engineering Exp: 1+ years in industry working with enzymes |
The protein engineering team works to address the complex challenges of enzyme discovery, characterization, and engineering. We utilize state-of-the-art computational software developed at Ginkgo to discover novel enzymes and employ cutting-edge software like Rosetta for rationally designing improvements. We want a person who is eager to learn and has a desire to utilize automation to work more efficiently | 7/18/2020 |
| 10562 | Genentech Hillsoboro, OR QC Lab Technician (Contract) AA degree in sciences Exp: 1 year in related |
Perform routine and semi-routine work that supports QC operations. Sampling and testing of utility systems (Color, Appearance, Odor, TOC, Conductivity, Bioburden, Endotoxin, Particulates and Moisture), facility monitoring (viable monitoring plates and non-viable particulate). Share maintenance responsibilities with other laboratory personnel such as reagent preparation, media growth promotion, and cleaning of incubators and biosafety cabinets. | 7/18/2020 |
| 10563 | Genentech Vacaville, CA Manufacturing Technician - BioProcess BS/BA in life sciences or engineering Exp: 0-2 years |
The Manufacturing Technician is responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment. The individual will be required to work in and maintain a clean room environment. Area of work must remain in a high state of inspection readiness at all times. | 7/18/2020 |
| 10564 | Genentech South San Francisco, CA PV Clinical Associate Health Care degree Exp: 0-2 years clinical experience |
Completes drug safety monitoring and tracking in a timely, thorough and accurate manner in accordance with pharmacovigilance (PV) and related standards, regulations and Genentech/Roche Standard Operating Procedures (SOPs). Reviews, evaluates and verifies potential AE information during Preliminary Assessment (PA) to determine required action per internal policies and procedures and perform data entry of adverse event by timely completion of the case via Roche global safety database. Performs seriousness / validity / causality and conducts quality review of all cases (as applicable) based on their medical assessment | 7/18/2020 |
| 10565 | Zynex Medical Champaign, IL Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 10566 | Zynex Medical Carbondale, IL Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 10567 | Zynex Medical Olney, IL Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 10568 | Zynex Medical Bismarck, ND Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 10569 | Zynex Medical Burlington, VT Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 10570 | Zynex Medical Jonesboro, AR Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 10571 | Zynex Medical Dallas, TX Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 10572 | 10x Genomics Pleasanton, CA Research Associate 2-Molecular Biology/Product Development MS in molecular biology, biochemistry, genetics or related Exp: 1+ year(s) |
We are seeking an outstanding Research Associate to join the Product Development group to support the development and commercial launch of new products. This is a unique cross-disciplinary position that will work closely with a variety of groups including Molecular Biology, Chemistry, Microfluidics, QC, and Manufacturing, to develop and validate novel reagents for the rapid expansion of 10x product lines. Candidates must have a broad working knowledge of molecular biology and be able to apply that knowledge creatively and independently in a fast-paced work environment. The successful applicant will have exceptional attention to detail and the ability to meticulously execute and analyze highly complex experiments. Previous industry experience is essential. etc. | 7/15/2020 |
| 10573 | 3T Biosciences South San Francisco, CA Research Associate, Protein Engineering MS Exp: 0-2+ year(s) |
Your Typical Responsibilities: Protein engineering to support TCR-T cell programs, and identify compounds with optimal therapeutic index. TCR engineering for improved efficacy, and specificity. Performing cell-based assays to test prospective optimized leads. Discovery of TCR mimetic (mTCR) compounds that bind selectively to pMHC targets identified at 3T. Improvement of existing yeast display platforms and development of next-generation pMHC libraries. etc. | 7/15/2020 |
| 10574 | Abbot Menlo Park, CA Assembler I - SECOND SHIFT HS diploma or equivalent Exp: 0-3 years |
Position Summary: Performs a wide variety of electronic, mechanical, or electro-mechanical assembly operations on assemblies or sub-assemblies. Sets up and operates automatic or semi-automatic machines. May perform other tasks including, but not limited to; placing labels on packages, and putting data sheets with product. Main Responsibilities: Assembles, repairs, inspect and/or test products following written instructions. Ability to read and comprehend basic instructions and other work related documents, written in English. Sets up and operates a variety of manufacturing machines or equipment following written instructions in the English language. etc. | 7/15/2020 |
| 10575 | Abbot Sylmar, CA Mechanical Development Quality Engineer I BS/MS in mechanical, system, or industrial engineering or related Exp: 0-2 years |
Analyze quality standards for components, materials or services. Apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met. We are seeking an experienced, high caliber Mechanical Development Quality Engineer to assure new or modified products conform to quality standards and establish compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs. Employees act on their strong desire to make a difference, partner with others and put ideas into action. Employees are engaged by a work culture that is team-oriented, fast paced and progressive. etc. | 7/15/2020 |
| 10576 | Abbot Plymouth, MN Analyst II, Product Surveillance BS in a healthcare, science or technical field Exp: Not necessary for BS candidates |
Postmarket Surveillance Analyst may perform two different functions within complaint handling. One role is that of complaint investigation management which includes all activities pertaining to receiving and investigating reports of worldwide complaints/events on a variety of products; entering information into the complaint database; independently determining and filing appropriate medical devices reports with various regulatory agencies; participating on cross-functional teams; and providing information on product complaints to various teams (e.g. Regulatory, Quality Engineering). The other role of the Postmarket Surveillance Analyst is performing evaluations on various types of returned complaint products (e.g. disposable and implantable products, electronic and electro-mechanical medical devices and systems) such as performing non-destructive and destructive testing; reviewing of Device History Records; etc. | 7/15/2020 |
| 10577 | Abbot Scarborough, ME Production Specialist II HS diploma or equivalent Exp: 1+ year(s) |
We have an exciting opportunity for a Production Specialist II within our Abbott Rapid Diagnostics business located at Scarborough, Maine. In this role, you will perform the work required for the assembly of components, devices, and/or the final product depending on the trade assigned. Abbott Rapid Diagnostics (formerly Alere) is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. RESPONSIBILITIES: Performs work required for the assembly of components, devices and/or the final product. Performs routine work in all production areas with limited supervision. etc. | 7/15/2020 |
| 10578 | Abbvie Cambridge, MA Associate Scientist II/Scientist I, In Vivo Pharmacology MS in biology or related Exp: 0+ years |
AbbVie is seeking an experienced, hands-on in-vivo scientist to join the In Vivo Pharmacology team at the Cambridge Research Center in Cambridge, MA. This individual will be responsible for designing and executing in vivo studies to support Parkinson’s Disease drug discovery projects. Key Responsibilities: Working closely with team members to design and execute in vivo experiments to support drug discovery efforts including target identification, target validation and efficacy of novel molecules. Developing new technologies and methods to understand disease pathophysiology and target biology. Responsible for implementation of in vivo studies and data collection as well as interpretation/analysis and presentation of results as needed. etc. | 7/15/2020 |
| 10579 | Abcam Eugene, OR Research Associate, Quality Control BS in biology or related Exp: 1+ year(s) |
We are seeking a Research Associate for our Quality Control team to test a wide variety of antibody-based products in our Eugene, OR facility. The core responsibility will be to provide support to the quality control team by testing our catalog of products after they have completed the manufacturing process. These products include quantity ELISA kits, activity ELISA kits, Western blot antibodies, immunocytochemistry antibodies, and flow cytometry kits. Primary Responsibilities: Perform documented methods required for finished product quality testing. Review manufacturing documentation for process deviations. Communicate analyzed results in detailed written reports. etc. | 7/15/2020 |
| 10580 | Abcam Burlingame, CA Manufacturing Associate Unspecified Exp: Entry level |
The successful candidate will undertake training in all procedures and work in compliance with Good Manufacturing Practices (GMP) defined under our Quality System Regulations and ISO13485 accreditations. In summary, the successful candidate will; Dilute and test antibody reagents for performance in immunohistochemical staining of tissues, according to approved procedures. Aliquot and package finished goods. Document test procedures, organize data and maintain accurate records of work performed according to GMP, QSR and ISO13485. Complete and review batch production records to provide cGMP documentation. Undertake stock-taking. etc. | 7/15/2020 |
| 10581 | Abzena Bristol, PA Bioconjugation Scientist MS in biochemistry, chemistry, protein chemistry or related Exp: 1-5+ year(s) |
Responsible for contributing to the optimization and development of bioconjugation techniques and related processes, including but not limited to the areas of Antibody Drug Conjugates (ADCs), protein drug conjugates, conjugated vaccine, Fluorescent-Probe Bioconjugation and Protein-Protein cross-linking. Typical Duties Include: Planning of synthetic routes/strategies, the execution and delivery of bioconjugation projects for Abzena’s clients. Preparation, purification and characterization of all materials including the protein and the drug molecules. Maintaining clear and current records of their work within a laboratory notebook and performing all applicable analytical work. etc. | 7/15/2020 |
| 10582 | Absorption Systems Exton, PA Associate Scientist / Scientist – Molecular or Immunology BS/MS Exp: 1-3 year(s) |
Absorption Systems, provides analytical support for gene and cell therapy products through every stage of development, is seeking a candidate for either an Associate Scientist position in molecular biology and gene expression at the headquarter location in Exton, Pennsylvania. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. Primary Responsibilities: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. Conducting studies on molecular biology assays, such as purification of DNA/RNA/Protein from samples, qPCR, protein assays. etc. | 7/15/2020 |
| 10583 | Wuxi AppTec King of Prussia, PA Associate Scientist Downstream Process Development MS in biology, biochemistry, immunology, bioengineering or related Exp: 0-2 years |
The successful candidate will be responsible for conducting experiments to support client-based processes with a focus on vaccine Downstream cell culture processes. This position will work with a team of scientists and technical specialists responsible for process development and technology transfer to ensure the application of well-designed unit operations for inclusion in routine manufacturing operations supplying clinical and commercial materials. Contributes to operations of development team, and may support tech transfer activities as necessary. Responsibilities: Work according to defined protocols on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. Execute lab-scale experiment in supporting downstream process development, verification, characterization. etc. | 7/14/2020 |
| 10584 | Wuxi AppTec Philadelphia, PA Manufacturing Associate I AS/BS Exp: 0-2 years |
Responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). Responsibilities: Understands aseptic technique concepts. Thorough understanding of Good Laboratory Practices and Good Manufacturing Practices. Able to operate and maintain equipment. Performs solution and material preparation. Possesses basic technical knowledge and background. etc. | 7/14/2020 |
| 10585 | Wuxi AppTec San Diego, CA Research Associate I BS in biology Exp: 0-1 year(s) |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate I to join the team. Responsibilities: Assist with in vivo pharmacology experiments for preclinical contract research. Perform in vivo studies to evaluate anti-cancer efficacy of test agents in tumor mouse models with supervision. Monitor mouse groups enrolled in drug efficacy, mechanism of action, PKPD and proof-of-concept studies. Perform drug dosing by various routes of administration. Perform in-life blood sampling through various routes. etc. | 7/14/2020 |
| 10586 | Wuxi AppTec San Diego, CA Research Associate II AS/BS in biology Exp: 1-3 year(s) |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking highly skilled and motivated Research Associate to join the team. Responsibilities: Conducting in vivo pharmacology experiments for preclinical contract research with minimal supervision. Assisting and performing efficacy and PK-PD studies and developing new in vivo/ ex vivo assays and models with minimum supervision, as needed. Help to design, optimize and execute of pharmacology experiments for compound screening, compound mode of action and efficacy in mechanistic and disease models, e.g. syngeneic and xenograft tumor model, acute and chronic autoimmune/inflammatory conditions, and analyses and reporting of experiments or implantation, blood/tissue collection, etc. | 7/14/2020 |
| 10587 | X-Chem Pharmaceuticals Waltham, MA Research Associate / Senior Research Associate BS/MS in biochemistry, chemistry, or related Exp: 1-3 year(s) |
X-Chem Pharmaceuticals is seeking candidates for the position of Research Associate / Senior Research Associate, Lead Discovery. X-Chem is a drug discovery company that uses DNA-encoded library (DEL) technology to discover leads for therapeutic targets. As a world leader in DEL technology, X-Chem collaborates with numerous pharmaceutical and biotechnology companies, resulting in over 70 licensed programs to date. Key Responsibilities: Determine suitability of constructs for affinity-mediated discovery processes. Use X-Chem’s DNA-Encoded Chemical Library technology to support a range of external projects. Assist in the interpretation of selection output data. Communicate observations, interpretations and conclusions internally and externally. etc. | 7/14/2020 |
| 10588 | Xellia Pharmaceuticals Cleveland, OH Aseptic Operator, IV Bag Manufacturing I HS diploma or equivalent Exp: 0-1 year(s) |
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator I is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. Key Responsibilities: Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. | 7/14/2020 |
| 10589 | Xellia Pharmaceuticals Cleveland, OH Inside Sales Representative - Southwest Territory (Remote) BS/BA Exp: 1-3 year(s) |
As a part of Xellia’s growing, energetic, and innovative pharmacy injectables sales seam, the Digital Sales Representative is responsible for driving sales to new customers while meeting established individual and organizational sales objectives. You will build and maintain valuable sales skills, cross-functionally learn about all facets of the business and help develop a pathway for growth opportunities and career advancement. Key Responsibilities: Manage, prospect, and build relationships within an assigned territory to drive new business, increase revenue growth and ensure customer satisfaction. Manage a sales pipeline, sales activity, and monthly business forecasting through customer interfacing activities and sales data analysis. Present regular updates to the Management team. etc. As a part of Xellia’s growing, energetic, and innovative pharmacy injectables sales seam, the Digital Sales Representative is responsible for driving sales to new customers while meeting established individual and organizational sales objectives. You will build and maintain valuable sales skills, cross-functionally learn about all facets of the business and help develop a pathway for growth opportunities and career advancement. Key Responsibilities: Manage, prospect, and build relationships within an assigned territory to drive new business, increase revenue growth and ensure customer satisfaction. Manage a sales pipeline, sales activity, and monthly business forecasting through customer interfacing activities and sales data analysis. Present regular updates to the Management team. etc. | 7/14/2020 |
| 10590 | Xellia Pharmaceuticals Cleveland, OH Aseptic Operator II - 12 Hour Shift HS diploma or equivalent Exp: 1-2 year(s) |
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator II is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. Key Responsibilities: Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. Documentation of perform tasks as per established Good Documentation Practices, and review of executed documentation (batch records, logbooks, etc.) in a timely manner. etc. | 7/14/2020 |
| 10591 | Xellia Pharmaceuticals Cleveland, OH Inside Sales Representative - Midwest Territory (Remote) BS/BA Exp: 1-3 year(s) |
As a part of Xellia’s growing, energetic, and innovative pharmacy injectables sales seam, the Digital Sales Representative is responsible for driving sales to new customers while meeting established individual and organizational sales objectives. You will build and maintain valuable sales skills, cross-functionally learn about all facets of the business and help develop a pathway for growth opportunities and career advancement. Key Responsibilities: Manage, prospect, and build relationships within an assigned territory to drive new business, increase revenue growth and ensure customer satisfaction. Manage a sales pipeline, sales activity, and monthly business forecasting through customer interfacing activities and sales data analysis. Present regular updates to the Management team. etc. | 7/14/2020 |
| 10592 | Xencor Monrovia, CA Laboratory Assistant BS/BA Exp: Entry level |
The Lab Assistant, Cell Biology is a temporary role in our Research facilities. Ours is a collaborative, agile environment requiring a sense of urgency, excellent work ethic and the ability to work efficiently and accurately. Responsibilities: Tissues culture with sterile technique. Experience with primary tissues and cell lines. Work with Peripheral Blood Mononuclear Cell (PBMC) is a plus. Maintain lab supplies. | 7/14/2020 |
| 10593 | Xeris Pharmaceutical Chicago, IL Desktop Support Technician (Temp to Hire) AS/AA in information technology or related Exp: 1-2 year(s) |
The Desktop Support Technician is responsible for supporting the organization’s end users via phone, email, and in person, in a dynamic, fast-paced environment. Strong customer service skills are a key component of this position which requires excellent communication and interpersonal skills, as well as the ability to resolve problems. Support may include but is not limited to hardware troubleshooting, software installations and/or configuration, imaging and deploying laptops/desktops, break/fix troubleshooting and end user education. This position will also require the ability to recognize root cause issues and document, resolve or escalate the root cause problem as necessary for resolution. The position will also require various other assigned tasks and responsibilities to be carried out as new projects and changes in the infrastructure occur. etc. | 7/14/2020 |
| 10594 | Yokogawa West Valley City, UT Service Project Engineer BS in computers and electronics, instrumentation technology, or related Exp: 1-3 year(s) |
Yokogawa is seeking to hire a Service Project Engineer. PRIMARY TASKS: Successfully execute multiple, small to moderate projects to the defined scope, within budget, on schedule, and to the satisfaction of the customer (internal and external). Conducts systems operational test. Installs system hardware/software upgrades as required. Manage and review the drawing package ACAD documentation. Review vendor submittals, prepare factory and other purchase orders, track orders, and receive materials per the project schedule and scope. Troubleshoot existing systems on-line and support network / subsystem testing. Provide regular updates on work in progress, immediate notification of issues related to quality, cost, or schedule, and propose solutions as problems arise. etc. | 7/14/2020 |
| 10595 | Yokogawa Newman, GA Assembler II HS diploma or equivalent Exp: 1-5 year(s) |
Description: Produce units based on an hourly production. Determine type of unit, parts necessary and production procedures to be followed for the required unit model by reading shop orders, Tokochu and work tags. Assemble instrument per established production procedures by using a variety of electric tools, gauges and hand tools. Accurately completes the needed data on all check sheets or any other required information. Maintain high quality level by using proper assembly and testing techniques. Carry out duties under NYPS system making suggestions and learning all process. Maintain a clean work area by continuous monitoring of assigned station. Must have high level of dexterity to perform with accuracy in producing required quantities of product, with emphasis in quality. etc. | 7/14/2020 |
| 10596 | Zoetis Eagle Grove, IA Production Operator HS diploma or equivalent Exp: 6+ months |
This position is responsible for operating process equipment and following all site operating, Quality, cGMP, and safety procedures associated with manufacturing of bulk medicated feed additives (MFA) from raw material to finished product. Incumbent must be able to clearly and frequently communicate with various functions within the site, including production, maintenance, quality operations, fermentation development, and administration. This is a 3rd shift position for the hours of 10:00 pm – 6:00 am. POSITION RESPONSIBILITIES: Selects and weighs components in accordance with established manufacturing directions (batch records). Selects and moves components to weighing area or dumping station. Examines finished products to determine consistency and blend characteristics. Samples products according to Quality Control procedures. Selects and records lot number and weights of all materials, reconciles weights and yields on batch formulation sheet. etc. | 7/14/2020 |
| 10597 | Zoetis Charles City, IA Refrigeration Specialist AS/AA in refrigeration, electricity, climate control or electronics Exp: 0-3 years |
Maintains, repairs and troubleshoots business operations objects which include and not limited to: Freeze dryers, Coolers, Freezers, Ultra low freezers, Chillers, HVAC units, Utilities equipment, Electrical systems, etc. Refrigeration Technician – Incumbents with refrigeration experience, use of tools and equipment and a wide variety of practices and procedures. As experience and competence is gained, assignments become more varied and are performed with greater independence. This class is flexibly-staffed with Refrigeration Technicians and incumbents may advance to the higher level after gaining the multi skills and experience which meet the qualifications for and demonstrating the ability to perform the work of the higher level class. etc. | 7/14/2020 |
| 10598 | Zoetis Charles City, IA Technical Process Specialist MS in microbiology, biological systems engineering, mechanical engineering or related Exp: 0-2 years |
Provide technical guidance on issues/projects within Manufacturing or Quality. Coordinate the engagement of the Global Manufacturing Technology (GMT) organization as needed. Identify and drive continuous process improvements. Lead large scale investigations for the site. Identify and implement cost savings initiatives for the site. Conducts all activities and makes decisions that are in accordance with Company policies & SOPs, Zoetis Values, & global regulatory guidelines (including cGMP/cGLP/cGCP), environmental guidelines, as appropriate, etc. Position Responsibilities: Take the manufacturing/quality lead in the introduction of new processes or modifications to existing processes as supported by Global Manufacturing Technology (GMT). Assist in performing technical evaluations and implementation of GMT initiatives to ensure robust process improvements and transfers. etc. | 7/14/2020 |
| 10599 | Zoetis Lincoln, NE Animal Laboratory Technologist HS diploma or equivalent Exp: 0-4+ years |
This position will support manufacturing in vivo potency and safety testing for product release, manufacturing investigations, and clinical research. The incumbent’s responsibility includes performing in vivo testing procedures, data collection, data audits, data entry/verification, some general care and husbandry of laboratory animals, performing test method investigations and assisting with research studies. Position Responsibilities: Perform routine laboratory testing. Test set-up / data audit/ data validation. Proficient with all injections [vaccinations / inoculations (IM, SQ, IP, ICr, IV), treatments (IM, SQ, orally, IV, topically)] and blood collections by all routes, as directed. Proficient with challenge techniques and post-challenge observations. Maintain required documentation for laboratory animal procedures (i.e. ACUPs, LIMS, SOPs). Assist with/perform laboratory animal testing associated with projects. Assist with trouble shooting and problem solving for assays and processes. etc. | 7/14/2020 |
| 10600 | Zoetis Lincoln, NE Packaging Technician – 2nd Shift HS diploma or equivalent Exp: 1-2 year(s) |
Work as part of a team operating pharmaceutical packaging lines. Operate packaging equipment and other related tasks. Maintain accurate and concurrent documentation of all tasks completed. Maintain a positive attitude and be able to work well with others in a team environment. Demonstrate good attendance. Position Responsibilities: Record Keeping and Documentation: Maintain and complete accurate records (time cards, batch records, log books, etc.). Equipment: Operate assigned equipment, i.e. . PLC controlled packaging line, vision system, etc. Clean production equipment and facilities. Set-up/ disassemble production equipment. Operate specific in-process devices associated with the equipment, i.e. moisture analyzers, pH meters, etc. | 7/14/2020 |
| 10601 | Zoetis Lincoln, NE Packaging Technician HS diploma or equivalent Exp: 6 months |
Position Responsibilities: Working with a coach and / or trainer complete the Packaging Operations On the Job Training Program which includes, but is not limited to the following: Complete Training Modules (Packaging Orientation, Packaging Safety, Packaging Safety Program, Packaging Colleague Expectations, and the department specific module for the packaging area assigned). Complete job specific training check lists for 5 packaging lines. Learn to use Packaging related Standard Operating Procedures, Batch Records, Log Books and Job Aides. Learn the operation of Motorized Materials Handling Equipment as assigned. Learn to identify packaging component and finished goods quality expectations. Learn to complete product specific packaging documents and log book entries. Learn the support of manufacturing departments through the movement of product, raw materials, and supplies in and out of the manufacturing areas. etc. | 7/14/2020 |
| 10602 | Zoetis Kalamazoo, MI Formulation Scientist MS in pharmacy, pharmaceutics, chemical engineering or related Exp: 0-5 years |
We are seeking formulation scientist to support development of new veterinary drug products and reformulation of existing products. The formulation scientist will be responsible for characterization of candidate molecules for the development of appropriate dosage forms for clinical and commercial needs. This is an exciting opportunity where scientist will have full ownership on formulation research in early stages as well as often late stage development. The scientist will be expected to support interdisciplinary teams of colleagues from Discovery, clinical development, safety, regulatory, marketing and global manufacturing, with technical expertise. On occasion, the scientist will be expected to lead PharSci team and bring forward the drug product, analytical methods and drug supplies for drug candidates from early discovery stage to commercialization. Working on veterinary medicine, the scientist will have opportunity to work on the development of oral, topical, parenteral and other delivery routes. etc. | 7/14/2020 |
| 10603 | Zymergen San Francisco, CA Chemistry Associate, Consumer Care MS in chemistry, chemical engineering, material science or related Exp: 1-2 year(s) |
Zymergen is looking for a Chemistry Associate with training and experience in Personal Care. The candidate will be a key contributor to the formulation efforts. The candidate will work closely with the project scientists to help drive the overall program progress on a technical level. Job Description: Experience in preparing lab batches and optimizing Home and Personal Care formulations under the scientist’s guidance. Experience in using rheometer to measure shear viscosity and tribology for understanding sensory attributes. If no experience in rheometer, passionate about learning how to use a rheometer. Carry out material characterisation such as pH, playtime, hydration, surface roughness and color change by X-rite, SPF, and viscometry. Document data entry of materials characterisation, pricing, formulations and SOPs. etc. | 7/14/2020 |
| 10604 | Wuxi AppTec San Diego, CA Research Associate I AS/BS in biology Exp: 0-1 year(s) |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate I to join the team. Responsibilities: Assist with in vivo pharmacology experiments for preclinical contract research. Perform in vivo studies to evaluate anti-cancer efficacy of test agents in tumor mouse models with supervision. Monitor mouse groups enrolled in drug efficacy, mechanism of action, PKPD and proof-of-concept studies. Perform drug dosing by various routes of administration. Perform in-life blood sampling through various routes. etc. | 7/14/2020 |
| 10605 | Fresenius Kabi Wilson, NC QC TECHNICIAN II BS/BA in chemistry Exp: 1-2 years lab experience |
Responsibilities include routine testing to support product release, raw material release, and cleaning verification. The technician will rely on experience and judgment in order to plan and accomplish goals. Routine testing of samples supporting incoming raw materials, in-process production, finished product, and validation. Utilize LIMS for data entry and test recording | 7/12/2020 |
| 10606 | Fresenius Kabi Lake Zurich, IL ASSOCIATE ELECTRONIC SUBMISSIONS SPECIALIST BS/BA Exp: 0-2 years in pharma |
Responsible for the electronic compilation and publishing of the company’s submissions to global drug, biological, and device regulatory authorities. Reporting to a Manager in Regulatory Affairs (RA), the position is responsible for the compilation and publishing of submissions to regulatory agencies. The position works with Plant and Corporate RA Specialists to obtain required documents. | 7/12/2020 |
| 10607 | Fresenius Kabi Grand Island, NY QC TECHNICIAN II - 1st Shift F,S,S,M Associates or BS/BA Exp: AS: 1-2 years, BS: 0 years |
This individual holding the position of QC Technician II shall be responsible for performing routine testing of in-process and finished product samples, raw material, stability, and utilities. They shall be responsible for monitoring the environmental conditions in the laboratory and in manufacturing areas. They shall support validation projects. This position must be available to work overtime as assigned. | 7/12/2020 |
| 10608 | Fresenius Kabi Canton, MA MANUFACTURING TECHNICIAN I (2nd shift) HS Diploma/GED Exp: 0-2 years industry experience |
Key Accountabilities include: Execution of routine production operations, labeling, quality control, inventory management, continuous improvement, maintenance of clean room equipment, carry out work in a safe manner while notifying management of safety issues and risks, assumes other duties and responsibilities as directed by supervisor. | 7/12/2020 |
| 10609 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift BS/BA or higher Exp: 1 or more years related experience |
Performs Method Transfers/method verifications/Co-Validations of testing procedures utilized within the Quality Control Laboratory. Prepares testing documentation or progress reports on projects and recommends course of future action. Acts as liaison between the Product Development, Stability, and the QC Chemistry Laboratories for the transfer and implementation of new procedures. | 7/12/2020 |
| 10610 | Fresenius Kabi Wilson, NC MANUFACTURING OPERATOR HS Diploma/GED Exp: 0-2 years |
Responsible for the daily coordination and sterilization of product. Performs Preventative Maintenance tasks on the terminal sterilizers. Responsible for sterilizer cycle review, troubleshooting of sterilizer problems, documentation of problems, and retrieval and delivery of product samples. Coordination with Maintenance personnel for repair of sterilizers. | 7/12/2020 |
| 10611 | Fresenius Kabi Grand Island, NY ASSOCIATE VALIDATION SCIENTIST BS/BA in sciences or engineering Exp: |
Responsible for providing technical support to operations in terms of equipment/system requalifications/ qualifications. Will perform studies as part of equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. Individual must also perform HEPA filter integrity/velocity testing and participates as hands-on work in critical area (class 100) airflow pattern testing. | 7/12/2020 |
| 10612 | Freudenberg Baldwin Park, CA Project Engineer I – Injection Molding BS/BA in engineering Exp: 1-2 years is engineering |
Work closely with project managers to gather/prepare all documentation relevant to a particular project. Responsible for Drafting and issuing validation protocols and production documents using information provided by customers and project managers. Responsible for gathering customer and technical information as required to make changes to documents or procedures at the customers request. | 7/12/2020 |
| 10613 | Freudenberg Carpinteria, CA Manufacturing Quality Engineer I BS in engineering or life sciences Exp: 1-3 years in regulated industry |
Responsible to provide Customer and Engineering feedback in regards to MSA, Critical to Quality Characteristics (CTQ’s) and Acceptance Activities. Lead Measurement System Analysis activities including Gage RnR, Test Method Validations, Test Procedures, etc. as part of the Design Transfer process. Provides all planning necessary to ensure effective product acceptance. This includes, but is not limited to, inspection instructions, equipment and gage requirements, and sampling plans. | 7/12/2020 |
| 10614 | Freudenberg Jeffersonville, IN Manufacturing Associate - 2nd Shift HS Diploma/GED Exp: 0 years |
Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements | 7/12/2020 |
| 10615 | Frontage Secaucus, NJ Lab Technician Medical Assistant certification Exp: 1-3 years in clinical research |
Develop a high level of familiarity and knowledge of the study protocol and flow chart of study procedures. Develop a strategy for implementing study procedures in compliance with study protocols. Performs laboratory procedures (g., preparation for admission testing, safety labs, and processing of biological specimen samples, shipment of samples and documentation of sample processing steps, etc.) as required by study protocol under the supervision of the Clinical Research Coordinator, Principal Investigator, and Sub-Investigators. | 7/12/2020 |
| 10616 | FujiFilm Diosynth Research Triangle park, NC Process Sciences Engineer II MS in biological or chemical sciences/engineering Exp: 0-4 years |
May support technical transfer of client project in and to manufacturing as applicable. Summarizes and report data. Interacts with supervisor and reports results and interpretation of experiments, project deliverables, and process readiness. Supports capital projects by providing technical expertise. Supports new project site-fit assessments as needed | 7/12/2020 |
| 10617 | FujiFilm Diosynth College Station, TX Validation Engineer I BS in engineering Exp: 0-2 years in validation |
Prepares and executes validation protocols. Prepares validation final report packages. Perform other duties as assigned | 7/12/2020 |
| 10618 | FujiFilm Diosynth College Station, TX Quality Control Analyst I Associates in chemistry or biochemistry Exp: 1-2 years in data review |
Review of QC analytical testing for GMP in-process, release and stability testing as needed: pH, Osmolality, Conductivity & qPCR, RP-HPLC, SEC, Agarose Gel Electrophoresis, UPLC, CE, IEF, Protein Purity Assays, Peptide Mapping, DNA Sequencing and/or UV/Vis Spectrometry preferred. Review technical transfer, qualification and validation protocols as needed. | 7/12/2020 |
| 10619 | FujiFilm Diosynth College Station, TX Microbiology Analyst I BS/BA or Associates in biology/chemistry Exp: 0-2 years |
Assist with QC microbiological aspects of cGMP compliance and testing. Assist manufacturing personnel in the identification of microbiological root cause analysis and provide technical advice as needed. Participate in the investigation and review of alert and action limit investigations as needed. Participate in cleaning and process validation activities involving microbiology. | 7/12/2020 |
| 10620 | FujiFilm Diosynth College Station, TX Downstream Manufacturing Technician I HS Diploma or Associates in biological sciences Exp: 0-1 years |
The Downstream Manufacturing Technician I will work directly with viral purification (either whole particle or split particle), continuous flow centrifuge operation, and sucrose gradient separation, techniques for filtration and chromatographic separation (i.e. column chromatography and HPLC) and viral inactivation. | 7/12/2020 |
| 10621 | FujiFilm Diosynth College Station, TX Cell Biology Analyst I BS in biology Exp: 0-2 years |
Assist with quality control analytical testing of samples provided to the QC laboratory. Assist with executing test qualification and validation of QC test methods. Writes and revises Standard Operating Procedures (SOPs) and other related Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP) documentation | 7/12/2020 |
| 10622 | FujiFilm Diosynth College Station, TX Automation Engineer BS in electrical/mechanical/chemical engineering Exp: 1 year |
Provide support on a daily basis to process control system, building management systems and data historian systems. Perform system software updates, security updates and upgrades to newer version. Support and enforce the data integrity program. Support and maintenance of computerized systems. Maintain Functional Specifications, Database Design Specifications and Hardware Design Specifications for automation systems. | 7/12/2020 |
| 10623 | Frontage Concord, OH Maintenance Technician HS Diploma/GED Exp: 1 year in facility services |
Assist in keeping building systems operational by completing assigned preventive maintenance requirements; following manufacturer’s instructions; troubleshooting malfunctions with oversight from supervisor and facilities staff. Assist in the maintenance and repair of various building equipment and systems including, but not limited to plumbing and piping systems, HVAC, electrical distribution, and boilers. | 7/12/2020 |
| 10624 | Eyevance Pharmaceuticals Fort Worth, TX Ophthalmic Territory Ranger BS/BA or equivalaent experience in sales/sciences Exp: 0-2 years |
Inside sales to white space and vacant territory business planning/support. Develop and maintain strong working relationships with target HCPs (via telephone, video conference and in person). Deliver approved, education-focused messages, as well as the assigned therapeutic area disease-state information to target HCPs (via telephone, video conference and in person). | 7/11/2020 |
| 10625 | Facet Medical Technologies Atlanta, GA Quality Engineer BS/BA in engineering or sciences Exp: 1-2 years in quality engineering |
The Quality Engineer plans and directs activities concerned with development, application, and maintenance of quality processes, materials, and products. Additionally, responsible for investigation manufacturing and customer nonconformance’s, determining root causes and corrective actions, reviewing and approving protocols and final reports and developing product specifications and sampling plans. | 7/11/2020 |
| 10626 | FHC Bowdoin, ME Product Development Engineer BS or better in biomedical, electrical or mechanical engineering Exp: 0-3 years |
The Product Development Engineer will contribute to all phases of product design, development and support. Technical competencies in the areas of biomedical engineering, electrical engineering and mechanical engineering are required. Maintain familiarity with relevant portions of the FHC Quality System and perform all duties within its guidelines, specifically those pertaining to design control, software development, EC’s and CAPA | 7/11/2020 |
| 10627 | FHC Bowdoin, ME Associate Manufacturing Engineer BS in engineering Exp: 0-2 years in process improvement |
The Associate Manufacturing Engineer works closely with Production, Quality, Materials and Engineering to help define and continually improve all manufacturing processes. This position will assist in resolving existing production issues, reviewing the existing process for improvement opportunities with regard to fixturing or other electrical/mechanical solutions, revising the process to ensure efficiency, and ensuring the process is accurately documented. | 7/11/2020 |
| 10628 | FHC Greenville, PA Production Technician HS Diploma/GED or Associates Exp: 0-2 years general experience |
The Production Technician assists FHC Greenville. This position involves some production duties, a variety of ERP System activities, and other general business office activities. Assemble product following work and print instructions as specified on manufacturing job orders generated from FHC’s ERP system. Relieve inventory physically and/or electronically through FHC’s ERP system if needed and follow the procedures to account for all items. | 7/11/2020 |
| 10629 | FHC Greenville, PA Manufacturing Support Specialist HS Diploma/GED or Associates Exp: 0-2 years general experience |
The Manufacturing Support Specialist assists GNS Production. This position involves some production duties, a variety of general accounting activities, and other general business office activities. Assists in performing secretarial, data entry and/or other general administrative tasks as required. Prepare and process Job order, Sales Orders. | 7/11/2020 |
| 10630 | Finch Cambridge, MA Clinical Assistant Certified medical assistant Exp: 1-2 years in health care |
A Clinical Assistant is responsible for a wide variety of clinical and clerical duties to support the Stool Donation program. The Clinical Assistant works under the general supervision of the Nursing and Supervising clinical staff is responsible for following Standard Operating Procedures to ensure the safety of stool donations. The Clinical Assistant will work collaboratively with donor operations staff and other departments to ensure strict adherence to standard operating procedures and maintain constant communication with clinical staff. | 7/11/2020 |
| 10631 | First Light Diagnostics Chelmsford, MA Research Technician Certification or AS in life sciences Exp: 1-2 years in life sciences research |
The Research Technician will work collaboratively with the research associates and scientists to support the development, verification, and validation of high performance immuno- and direct cell detection-based assays in preparation for FDA submission. S/he will manage laboratory inventory, ensure proper maintenance and calibration of laboratory equipment, and prepare common reagents used by the team. | 7/11/2020 |
| 10632 | Forma Therapeutics Watertown, MA Research Associate, Translational Science BS or MS in biology or realted Exp: 1-2 years in drug discovery/sciences |
Develop, optimize and perform assays using molecular biology procedures and technologies including qPCR, quantitative western blots, ELISA. In vitro culture of cancer cell lines and primary cells as well as DNA/RNA isolation from blood/tissue is required. Assist in the management of preclinical and clinical samples internally and with third party providers. | 7/11/2020 |
| 10633 | Foundation Medicine Cambridge, MA Bioinformatics Scientist I MS in biological/chemical/computer sciences Exp: 1+ years in industry or academic center |
The Scientist I, Bioinformatics develops novel methods for detecting, reporting and analyzing alterations in tumor DNA and RNA, while optimizing existing methods. The incumbent provides scientific and technical contributions for a designated project on an interdisciplinary team. The Scientist I, Bioinformatics is also responsible for supporting novel biomarker and companion diagnostics development by mining and analyzing various types of data generated during the product development and validation process. | 7/11/2020 |
| 10634 | Foundation Medicine Cambridge, MA Accessioning Technician II BS/BA in life sciences Exp: 0-1 years in CLIA lab |
The Accessioning Technician II performs critical sample receipt and data entry functions in FMI’s CLIA-certified clinical laboratory. Specifically, the Accessioning Technician II receives incoming samples and ensures that necessary information has been received to move forward with processing. The Accessioning Technician II is assigned to one of three shifts and may be assigned to work any day that the lab is operational. | 7/11/2020 |
| 10635 | Foxx Life Sciences Salem, NH WarehouseAssociate HS Diploma/GED or Associates Exp: 0-2 years, Entry Level |
Foxx Life Sciences is facing overwhelming demand for our products and is seeking entry-level, full-time, hourly WarehouseAssociates to assist with specific, daily functions within general manufacturing and assembly. There will be future possibilities for promotions as the company grows. All training is provided,and prior experience is not required for consideration. | 7/11/2020 |
| 10636 | Freenome South San Francisco, CA Clinical Laboratory Associate BS/BA in life sciences Exp: 1-2 years, knowledge of lab regulations |
Freenome’s Clinical Laboratory Associate will support the company’s Pre-Analytical Laboratory with the receiving, accessioning, plasma sample processing, and storage. Important to our mission is providing quality samples to process downstream for quality analysis and results.Verifies all aspects of incoming specimens and assess acceptability for testing | 7/11/2020 |
| 10637 | FreeThink Technologies Branford, CT Laboratory Scientist, Analytical Sciences BS or MS in chemistry or chemical engineering Exp: 1-2 years in pharma preferred |
Analyze products to determine chemical and physical properties following Company, client and Pharmacopeial methodologies with minimal supervision. Ensure all work performed is in compliance with standard operating procedures, good laboratory practices and good manufacturing practices. Document laboratory work concurrently in a clear, detailed and organized manner | 7/11/2020 |
| 10638 | Foundation Medicine Cambridge, MA CAPA Coordinator BS in related field Exp: 1-2 years in QA or medical/pharma |
The CAPA Coordinator assists with the CAPA System at FMI and supports with day to day administration of the CAPA process, documentation, and retention of the quality records. The Coordinator is responsible for expediting and coordinating a multitude of interrelated project activities pertaining to different daily tasks with changing priorities to ensure the successful completion of CAPA work stream. This position interacts with all departments within FMI. | 7/11/2020 |
| 10639 | Fate Therapeutics San Diego, CA Process Development Engineer, MSAT MS in biological or chemical sciences/engineering Exp: 1 year in biopharma |
The candidate will assist seniormembers of the MSAT teamin thedevelopment ofscaled-upculture, differentiation, purification and characterization methods foriPSC-derived cellulartherapy products. Furthermore,they will activelysupport laboratory operations by coordinating the inventory,purchaseandaliquoting of key reagents. | 7/11/2020 |
| 10640 | Molecular Devices San Jose, CA New Product Introduction Engineer, BioImaging BS in engineering Exp: 1-4 years (interships included) |
The NPI Engineer supports all aspects of the product development process, from concept definition through production transfer, training, and support with a focus on delivering manufacturability, serviceability, and reliability throughout the product lifecycle. Manage the prototype assembly process and tooling readiness. Qualify key technology suppliers and facilitate the R&D supply chain | 7/11/2020 |
| 10641 | Translate Bio Lexington, MA Research Associate I/II, Cell Biology BS/MS Exp: 0-5 years |
We are seeking a highly motivated, organized individual with demonstrated competencies/ability to learn new cell-based assays quickly. The successful candidate will join the fast-growing, vibrant Biology Team. She/he will be conducting innovative research in the discovery pipeline, aiding the advancement of several key programs through method development for both in vitro and in vivo studies. These activities particularly include differentiating iPSC lines for in vitro lung disease-modelling and drug screening studies. The environment nurtures innovation, and encourages career growth, therefore the individual will have the opportunity to learn a range of novel cell and molecular biology techniques. etc. | 7/8/2020 |
| 10642 | Tris Pharma Monmouth Junction, NJ QC Chemist BS in chemistry or related Exp: 0-3 years |
The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies, collaborates closely with and under the direct supervision of Senior QC Analytical Chemists, Team Leads, and QC Managers. The incumbent carries out laboratory work to support QC activities and performs special projects as assigned. Carries out responsibilities in accordance with the organization’s policies, SOPs, and state, federal and local laws. Performs testing of raw materials, IP, FP and/or ST samples including dissolution, assay, content/blend uniformity, particle size distribution, and other tests according to the analytical methods, United States Pharmacopeia (USP) procedures in a regulated laboratory environment. etc. | 7/8/2020 |
| 10643 | Tris Pharma Monmouth Junction, NJ AR&D Scientist I BS in chemistry or related Exp: 1+ year(s) |
The Analytical Research and Development (AR&D) Scientist performs laboratory analyses in the testing of raw materials, in process (IP), finished products (FP) and stability (ST) samples following Analytical Methods, Protocols, Standard Operating Procedures (SOPs) and company policies. Collaborating closely with, and under the direct supervision of, Senior AR&D Scientists and AR&D Managers the incumbent carries out laboratory work to support AR&D activities and performs special projects as assigned. She/he also carries out laboratory work to support product development and method development. Carries out responsibilities in accordance with the organization’s policies, SOPs, and state, federal and local laws. Operates general analytical instruments during raw material, IP and FP testing such as High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC,), Ultra Violet visible spectroscopy (UV/Vis), automatic titration, Infra Red Spectroscopy (IR), Atomic Absorption (AA), Thin Layer Chromatography (TLC) and dissolution apparatus. etc. | 7/8/2020 |
| 10644 | Vapotherm Exeter, NH Quality Engineer I BS in engineering or science Exp: 1-2 year(s) |
The Quality Engineer will be responsible for representing quality on projects and overall quality support to the organization including implementation of Vapotherm’s Quality Management System. Primary Responsibilities: Participate in the execution of Quality functions in compliance with FDA QSRs, ISO 13485, ISO 14971, IEC 60601, MDD, EU-MDR, CMDR, CMDCAS and other national and international quality requirements and standards. Assists in reviewing and executing design and process verifications and validations, inclusive of IQ/OQ/PQ/V&V protocol and report documentation. Cross-Functional team member assisting in product design control activities. etc. | 7/8/2020 |
| 10645 | Vericel Cambridge, MA QC Analyst I BS/BA Exp: 1 year |
Perform routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation. Core Responsibilities: Perform microbiological assays for in-process and final product samples. Perform analytical methods for final bulk material/finished goods. Test and disposition of raw materials and perform environmental monitoring. Review of QC data for compliance to procedures and specifications. Calculate and evaluate results. Participate in lab maintenance and administration duties. Initiate lab investigations and deviations. Lab support including but not limited to glass washing, autoclaving, etc. Effectively demonstrate an understanding of CGMPs and how it applies to specific responsibilities. etc. | 7/8/2020 |
| 10646 | Vericel Cambridge, MA Manufacturing Technician BS/BA Exp: 0-2 years |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. Core Responsibilities: Perform manufacturing procedures inside an ISO Class 7 clean room in accordance to established SOPs, cGMPs, and safety regulations. Perform aseptic manipulations of cell culture lots and final product assemblies. Document production operations in corresponding batch records and log sheets according to cGMPs and established SOPs. Input data from production records to existing databases. General housekeeping of manufacturing controlled areas. Perform clean room equipment sanitization. etc. | 7/8/2020 |
| 10647 | Viant Upland, CA Quality Inspector/Technician - 2nd Shift unspecified Exp: 1+ year(s) |
The Quality Inspector/Technician is responsible for determining if product manufactured conforms to specified requirements. This shall be accomplished by inspecting, monitoring and releasing to established acceptance criteria. This position shall also ensure that quality related functions, procedures and policies established are adhered to. POSITION REQUIREMENTS: Conduct first article inspection for start-up processes. Conduct in-process inspection of manufacturing and assembly processes. Conduct final inspection (AQL) for lot release. Communicate with Lead Inspector and production personnel on non-conformances found. Coordinate retained parts with proper identification. Audit production operations. etc. | 7/8/2020 |
| 10648 | Visterra Waltham, MA Research Associate BS in biology, biochemistry, biological engineering, or related Exp: 1+ year(s) |
Visterra, Inc., needs a highly motivated Research Associate with research experience in biochemistry, protein sciences and/or molecular biology to help further our antibody-based drug discovery programs. This individual will play a key technical role in advancing Visterra’s early research programs targeting challenging diseases including chronic pain, kidney disease, autoimmunity, and other related areas of therapeutic interest. The candidate will utilize library-based screening methods, recombinant protein production, protein engineering, and various biochemical and analytical methods to characterize early and late stage drug candidates. The ideal candidate should have a B.S. degree in biology, biochemistry, biological engineering or related field and a minimum of one year "at the bench "research experience. etc. | 7/8/2020 |
| 10649 | Vor Cambridge, MA Associate Scientist, Cancer Immunotherapy MS in biology, immunology, cancer biology or related Exp: 1+ year(s) |
Vor Biopharma is seeking a motivated Associate Scientist to join our Cancer Immunotherapy group. This individual will be independent, goal-oriented, technically competent, and able to efficiently in a team setting. We are searching for enthusiastic, innovative, and inquisitive individuals with deep scientific background in immunology, cancer immunotherapy, and/or autoimmune diseases, who are comfortable working in a fast-paced entrepreneurial environment. Key areas of responsibility: Work closely with a diverse team of scientists to drive key cancer immunotherapy projects forward. Design and execute experiments for in vitro, in vivo, and ex vivo immune studies. Phenotyping immune populations, sample preparation, and analysis for in vivo studies. Data analysis and proper electronic notebook record keeping. Communication of experimental plans and data within the team. etc. | 7/8/2020 |
| 10650 | Wave Life Sciences Cambridge, MA Research Associate, Biology BS/MS in biology or related Exp: 0-3 years |
WAVE Life Sciences USA seeks a highly motivated biologist to join its research team in Boston, Massachusetts. This is an ideal position for an individual who is interested in learning cutting edge technologies and who thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate will be responsible for designing, executing and analyzing experiments as a member of teams focused on advancing therapeutic programs and discovery research platforms. This candidate will contribute to all levels of in vitro and in vivo discovery research to support development of optimized nucleic acid therapies in multiple disease areas. Prior experience in tissue processing are preferred, but not required. etc. | 7/8/2020 |
| 10651 | Wright Philadelphia, PA Material Handler I - Philadelphia, PA HS diploma or equivalent Exp: 1+ year(s) |
Wright Medical is hiring a Hub Material Handler I in Philadelphia, PA . The Hub Material Handler I is responsible for making pickups and deliveries of implants and instruments to and from local hospitals, surgery centers, clinics/doctor’s offices, the airport, bus station, and other locations for expedited shipments. Excellent communication must be maintained with adaptability to the needs of the customers, sales management/reps, and both corporate and office personnel to ensure timely transportation of goods for surgical procedures. This position has responsibilities to be the liaison between the field office and Wright Medical customers for coordinating activities relating to the efficient use of company assets. A positive and professional approach is required with very strong communication skills to ensure a flawless delivery for surgery. etc. | 7/8/2020 |
| 10652 | Wuxi AppTec Marietta, GA Associate Laboratory Technician AS/BS Exp: 0-1 year |
We have an opening in our General Micro Department for an Associate Lab Technician. Responsibilities: Assist with the monitoring of inventory of basic laboratory supplies. Perform sample generation in STARLIMS system. Performs Gram stains and sub-culturing of client samples with accuracy. Maintain traceability of client isolates for Gram staining and Identification. Perform biochemical tests on isolates. etc. | 7/8/2020 |
| 10653 | Wuxi AppTec San Diego, CA Process Engineer BS/MS in chemical engineering or related Exp: 1-2 year(s) |
The Process Engineer prepares GMP documentation such as batch/cleaning records, equipment qualification protocols, campaign reports, etc. for the Pilot Plant and Kilo Lab. Prepares QA documents such as SOPs/TWIs to ensure cGMP compliance. Evaluates and improves current procedures and equipment in the Pilot Plant. Interacts with QA, QC, Process R&D, Materials Management, EH&S, Facilities, and Purchasing to optimize and execute manufacturing campaigns. Assists with the execution of GMP and non-GMP production in the Pilot Plant and Kilo Lab. Performs safety testing (DSC, RC-1, TSU, etc.) and other tests to collect and analyze data for project support. etc. | 7/8/2020 |
| 10654 | Wuxi AppTec Philadelphia, PA Laboratory Technician II BS in biology, chemistry, or related Exp: 1-2 year(s) |
Laboratory Technician II in Molecular Biology will be responsible for performing nucleic acid based assays where proficiency in nucleic acid extraction methods and qPCR is required. Experience in a GMP and/or high throughput lab where day to day activities are heavily driven by meeting deadlines is preferred. Independent data analysis experience preferred. Experience with automation and LIMS systems a plus. Responsibilities: Performs assays and lab procedures according to and in compliance with cGMP, CFR and/or PTC guidelines, and SOPs using appropriate laboratory techniques for the lab group assigned to. Performs laboratory support functions (e.g. inventory management and equipment calibration) to help ensure lab is operational; contributes to the overall operations and to the achievement of departmental goals and objectives. etc. | 7/8/2020 |
| 10655 | Upsher-Smith Maple Grove, MN CNS Field Sales Representative - Connecticut BS/BA in business, communications, marketing or related Exp: 1-3+ year(s) |
The CNS Field Sales Representative - Connecticut is responsible for the development and management of a designated territory with the goal of maximizing sales while improving patient lives. Patients are central to all our strategies and the Representative will be responsible for a physician and patient centric focus. The role is responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other identified healthcare practitioners and members of the health care community. The time allocation for this role is 70% field based selling and 30% utilization of virtual technology and inside approach to remote customer contact, however, this may vary as business needs arise. etc. | 7/8/2020 |
| 10656 | Upsher-Smith Baltimore, MD CNS FIeld Sales Representative - Maryland BS/BA in business, communications, marketing or related Exp: 1-3+ year(s) |
The CNS Field Sales Representative - Baltimore, MD is responsible for the development and management of a designated territory with the goal of maximizing sales while improving patient lives. Patients are central to all our strategies and the Representative will be responsible for a physician and patient centric focus. The role is responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other identified healthcare practitioners and members of the health care community. The time allocation for this role is 70% field based selling and 30% utilization of virtual technology and inside approach to remote customer contact, however, this may vary as business needs arise. etc. | 7/8/2020 |
| 10657 | Upsher-Smith Plymouth, MN Maintenance & Automation Technician/Mechanic - 2nd shift AS/AA Exp: 1 year |
The Maintenance & Automation Technician/Mechanic - 2nd shift repairs, maintains and assists manufacturing & packaging operations to ensure automated packaging line and large-scale manufacturing equipment is maintained. Troubleshoots, diagnoses, repairs and maintains manufacturing pharmaceutical manufacturing and packaging equipment/machinery. Follows all required safety practices and completes required documentation to ensure compliance to cGMP's. Essential Duties: Effectively troubleshoots and resolves automated machinery/mechanical equipment issues utilizing a systematic logical approach until the root cause is identified. Completes work orders and preventative maintenance tasks using fundamental, mechanical applied knowledge and experience. etc. | 7/8/2020 |
| 10658 | Stratos Genomics Seattle, WA Research Associate/Scientist—Molecular Engineering BS/MS in chemistry, organic chemistry, chemical engineering, or related Exp: 1-2 year(s) |
We are seeking driven, self-motivated, and passionate Research Associates/Scientists to join our team. Candidates will be involved in synthesizing the unique building blocks for our novel DNA sequencing technology, developing and optimizing synthesis protocols, as well as proposing and executing innovative experiments to push our technology forward. The position is salaried with hours dependent on lab needs and project deadlines. etc. | 7/7/2020 |
| 10659 | Structure Medical Naples, FL Swiss CNC Machinist I HS diploma or equivalent Exp: 1+ year(s) |
Performs entry level specialized computer numerical control (CNC) machinist work for Structure Medical, LLC. Operates CNC machines to run production per approved schedule provided. Work is performed under close supervision with minimal latitude for the use of initiative and independent judgment. Responsible for setting up and operating CNC machines; performs preventative maintenance on machines. Notifies the CNC Programmer of problems with equipment and/or tooling that may cause defects or lost time. Recommends process improvements to resolve problems. Fills out proper paperwork per job. etc. | 7/7/2020 |
| 10660 | Stryker Los Angeles, CA Associate Sales Representative BS/BA Exp: 1-2 year(s) |
As a Surgical Technologies Associate Sales Representative, you assist in strategically promoting and selling Stryker Surgical Technologies products to meet our customers’ needs. You confidently conduct product evaluations in Operating Room and office settings, persuasively demonstrating the value of our products. Systematically tracking your territory progress, you proactively communicate your findings with your Regional Manager and Sales Representative(s) you are supporting to push yourself to exceed each goal. When onsite with clients, you use your product knowledge and quick thinking to solve product problems and inform doctors, nurses and other staff as to the proper use and maintenance of our products. etc. | 7/7/2020 |
| 10661 | Stryker Indianapolis, IN Associate Sales Representative BS/BA Exp: 1+ year(s) |
You’ll work closely with experienced Sales Representatives and Managers to build your knowledge, skill and comfort with clinical and product knowledge as well as selling styles and techniques. They will serve as your coaches and mentors to share lessons learned for how to build and grow a successful business. You’ll receive training and be expected to study and prepare independently to perform at the highest levels in the operating room, working amongst surgeons and healthcare professionals. The expectations are challenging, yet rewarding. You’ll represent Stryker as a leader in our industry and the marketplace. etc. | 7/7/2020 |
| 10662 | Synlogic Cambridge, MA BioProcess Development Engineer BS in biology, bio-chemical engineering, or related Exp: 0-3 years |
We are currently seeking a highly motivated and enthusiastic BioProcess Engineer to contribute to development of fermentation and downstream processes for manufacturing of our engineered probiotics. The successful candidate will be part of a dynamic and motivated development team, helping to bring Synlogic’s novel synthetic biotics to clinical trials and eventual commercialization. HOW YOU WILL CONTRIBUTE: Lab operations to support microbial fermentation process development, optimization, and validation. Support and perform fermentations in benchtop bioreactors, high throughput fermentation systems (AMBR250, AMBR15), and large-scale single-use fermenter systems. etc. | 7/7/2020 |
| 10663 | Synlogic Cambridge, MA Laboratory Technician - In Vivo Operations AS/AA in animal or life science Exp: 1+ year(s) |
Synlogic is seeking a highly motivated Research Associate to join the Biology team. You will be supporting the Biology team by ensuring the proper care of our research animals and assist in vivarium operations. You will also participate in study activities including rodent handling, restraint, weighing, dosing, and sampling. This position will be a part-time position on a shift schedule supporting the Animal Care facility. Key Responsibilities: Perform husbandry duties of experimental rodents such as feeding and caring for animals, changing cages, and maintaining veterinary, animal inventory, and animal identification records Perform cleaning and sanitation of animal facility and equipment. etc. | 7/7/2020 |
| 10664 | Talis Menlo Park, CA Scientist - Assay Development MS in cellular or molecular biology Exp: 1-3 year(s) |
Reporting to the Associate Director, join the Assay Development group in the R&D division. We are a team of outstanding, dedicated scientists. We are seeking talented, motivated and driven individuals to join a collaborative effort to enable development of rapid diagnostic tests. This opportunity is in the fields of molecular diagnostics and leverages our proprietary microfluidic system. This position is an opportunity for the appropriate candidate to further develop independent thinking, creativity and leadership. You will develop additional menu(s) for our system. etc. | 7/7/2020 |
| 10665 | Talis Menlo Park, CA Research Associate - Assay Development MS in biology, microbiology, molecular biology, biochemistry or related Exp: 0-3 years |
The candidate will join the Assay Development group in the R&D division where focus is on molecular assays development such as nucleic acid isolation, purification, amplification and labeling technologies. We are seeking talented, motivated individuals to join a collaborative effort to enable development of rapid diagnostic tests of several pathogens from various clinical specimens. Position Responsibilities: Work under direction of senior scientists to run hands-on experiments for microbiology, sample preparation, nucleic acid extraction and amplification. Participate in design of molecular assays. Perform data analysis of experiments using Minitab or similar tools and develop summaries for the Assay Development group. etc. | 7/7/2020 |
| 10666 | Tempus Chicago, IL Clinical Molecular Technologist MS in medical technology, clinical laboratory science, molecular biology, or other science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. etc. | 7/7/2020 |
| 10667 | Tempus Chicago, IL Account Associate - Chicago BS in biology, life science, business or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). Coordinating Medical Affairs report review with physicians after clinical orders. Order Kit and literature replenishment at accounts. Identifying and attending approved local conferences. etc. | 7/7/2020 |
| 10668 | Tempus Atlanta, GA Clinical Laboratory Scientist (11:00am – 7:00pm shift) BS/MS in a biological science Exp: 1+ year(s) |
Responsibilities and Duties: Adhere to and follow laboratory established procedures for processing, analyzing and reporting patient samples. Follow laboratory established quality control policies and protocols in recording readings, note deviations and document all corrective actions taken when deviations occur. Be capable of identifying problems that may affect test performance and turnaround time and immediately bring it to supervisor, Director, or Medical directors’ attention. Be proficient in a wide range of routine and complex assays performed at AKESOgen with appropriate training. Be willing to run automated Nucleic Acid instrumentation, real time PCR, DNA/RNA spectrometer, genetic scanners, and other instruments with appropriate training. Assist in performing proficiency testing as required. etc. | 7/7/2020 |
| 10669 | Tempus Atlanta, GA Molecular Scientist BS/MS in a biological science Exp: 1+ year(s) |
Responsibilities and Duties: Adhere to and follow laboratory established procedures for processing, analyzing and reporting patient samples. Follow laboratory established quality control policies and protocols in recording readings, note deviations and document all corrective actions taken when deviations occur. Be capable of identifying problems that may affect test performance and turnaround time and immediately bring it to supervisor, Director, or Medical directors’ attention. Be proficient in a wide range of routine and complex assays performed at AKESOgen with appropriate training. Be willing to run automated Nucleic Acid instrumentation, real time PCR, DNA/RNA spectrometer, genetic scanners, and other instruments with appropriate training. Assist in performing proficiency testing as required. etc. | 7/7/2020 |
| 10670 | Tempus Atlanta, GA Clinical Laboratory Scientist (3:00pm – 11:00pm shift) BS/MS in a biological science Exp: 1+ year(s) |
Responsibilities and Duties: Adhere to and follow laboratory established procedures for processing, analyzing and reporting patient samples. Follow laboratory established quality control policies and protocols in recording readings, note deviations and document all corrective actions taken when deviations occur. Be capable of identifying problems that may affect test performance and turnaround time and immediately bring it to supervisor, Director, or Medical directors’ attention. Be proficient in a wide range of routine and complex assays performed at AKESOgen with appropriate training. Be willing to run automated Nucleic Acid instrumentation, real time PCR, DNA/RNA spectrometer, genetic scanners, and other instruments with appropriate training. Assist in performing proficiency testing as required. etc. | 7/7/2020 |
| 10671 | Tempus Atlanta, GA Clinical Laboratory Scientist (9:00am – 5:30pm shift) BS/MS in a biological science Exp: 1+ year(s) |
Responsibilities and Duties: Adhere to and follow laboratory established procedures for processing, analyzing and reporting patient samples. Follow laboratory established quality control policies and protocols in recording readings, note deviations and document all corrective actions taken when deviations occur. Be capable of identifying problems that may affect test performance and turnaround time and immediately bring it to supervisor, Director, or Medical directors’ attention. Be proficient in a wide range of routine and complex assays performed at AKESOgen with appropriate training. Be willing to run automated Nucleic Acid instrumentation, real time PCR, DNA/RNA spectrometer, genetic scanners, and other instruments with appropriate training. Assist in performing proficiency testing as required. etc. | 7/7/2020 |
| 10672 | Tempus Atlanta, GA Clinical Laboratory Scientist (AKESOgen) BS/MS in a biological science Exp: 1+ year(s) |
Responsibilities and Duties: Adhere to and follow laboratory established procedures for processing, analyzing and reporting patient samples. Follow laboratory established quality control policies and protocols in recording readings, note deviations and document all corrective actions taken when deviations occur. Be capable of identifying problems that may affect test performance and turnaround time and immediately bring it to supervisor, Director, or Medical directors’ attention. Be proficient in a wide range of routine and complex assays performed at AKESOgen with appropriate training. Be willing to run automated Nucleic Acid instrumentation, real time PCR, DNA/RNA spectrometer, genetic scanners, and other instruments with appropriate training. Assist in performing proficiency testing as required. etc. | 7/7/2020 |
| 10673 | Therapyx Buffalo, NY Laboratory Technician I BS/MS in a biological science Exp: 1+ year(s) |
We are seeking a talented and highly motivated Research Technician to assist in a bacterial infection project. The contributions made by this technician will support multiple aspects of the project through data collection, analysis and documentation. The successful candidate will possess the ability to work within a fast-paced multidisciplinary environment to effectively advance drug and vaccine development. PRIMARY RESPONSIBILITIES: Generation of data sets through strict adherence to established SOPs. Documentation and organization of experiments, data, inventory and other records as needed. etc. | 7/7/2020 |
| 10674 | Tenaya Therapeutics South San Francisco, CA RA I/II, Gene Therapy BS/MS in biology, biochemistry, or related Exp: 1+ year(s) |
Tenaya has an immediate need for a Research Associate I/II to support the Gene Therapy Research team. Tenaya is seeking a creative, self-motivated individual with a passion for experimental science and teamwork. The ideal candidate is a self-starter and problem-solver who will work closely with the team to drive the company’s future success. Key Responsibilities: Execute a diverse range of cell-based and molecular assays to characterize lead gene therapy candidates. Functionally assess transduction and other gene therapy mechanisms in vitro and in vivo. etc. | 7/7/2020 |
| 10675 | Stryker Albany, NY Associate Mako Product Specialist BS/BA Exp: 1 year |
In this role, you’ll be responsible for helping surgeons use Stryker’s Mako robot– our newest product used in robotic-arm assisted surgery. Acting as a helpful source for all things related to the Mako, you’ll provide clinical support to all end-users, offer guidance and assistance during surgical procedures, and resolve technical product and service issues as needed. In addition, you’ll also provide customer education and ongoing in-services, such as assisting surgeons in pre-operative implant planning. We’ll count on your attention to detail to ensure all cases are planned and reviewed with surgeons prior to scheduled surgeries, and that all inventory is accounted for. etc. | 7/7/2020 |
| 10676 | Stryker Columbus, OH Associate Sales Representative BS/BA Exp: 1-2 year(s) |
As a Spine Enabling Technologies Associate Sales Representative, you assist in strategically promoting and selling Stryker Spine Enabling Technologies products to meet our customers’ needs. You confidently conduct product evaluations in Operating Room and office settings, persuasively demonstrating the value of our products. Systematically tracking your territory progress, you proactively communicate your findings with your Regional Manager and Sales Representative(s) you are supporting to push yourself to exceed each goal. When onsite with clients, you use your product knowledge and quick thinking to solve product problems and inform doctors, nurses and other staff as to the proper use and maintenance of our products. etc. | 7/7/2020 |
| 10677 | Stryker Raleigh, NC Clinical Sales Representative - Endoscopy BS/BA Exp: 1-2 year(s) |
RESPONSIBILITIES: Drive continuous expansion of SPY Elite, SPY PHI and PINPOINT IMAGING SYSTEMS’S imaging system’s customer base in hospitals to achieve sales goals. Partner with multiple Sales Representatives to pull through usage of installed PINPOINT devices across multiple surgeon specialties. Become a Stryker expert across all imaging platforms, procedures, industry trends and competitive issues. Develop strong relationship with the Endoscopy and Regional Capital sales representatives. Drive adoption and usage of DermACELL advanced decellularized dermis in hospitals for use in various reconstructive applications. etc. | 7/7/2020 |
| 10678 | Stryker Scottsbluff, NE Joint Replacement Sales Associate BS/BA Exp: 1+ year(s) |
What you will do: Increasing Joint Replacement sales through assisting the sales teams and building own accounts by means of working with existing customers as well as identify new customers in order to grow their territory. Communicating with current and new Joint Replacement customer accounts regarding a variety of topics including product updates, changes to product portfolio and educational programs. Learn or hone selling skills and processes by coaching/mentoring support from Joint Replacement Sales Representatives and Managers. etc. | 7/7/2020 |
| 10679 | Stryker Chicago, IL Trauma Sales Associate BS/BA Exp: 1+ year(s) |
What you will do: You will get exposure to the proven winning Stryker Trauma culture that delivers Industry leading results in all market segments. You will receive best-in-class formal Trauma training on product portfolio and selling skills which includes on-the-job training in the operating room. You’ll become an expert on surgical procedures by observing well-over 300 cases in your first year. You will develop well-rounded field exposure to prepare you in all aspects of the selling/ servicing process when a territory opportunity arises. etc. | 7/7/2020 |
| 10680 | Synthego Redwood City, CA Factory Service Engineer, Generalist BS in biology, biomedical engineering, or related Exp: 1+ year(s) |
Join our operations team as a Factory Service Engineer-Generalist working to fully automate genome engineering. You will be a key member of the Service Engineering team responsible for characterizing and modifying core automated workflows, developing equipment documentation and SOPs, recommending advanced automation equipment as well as their acceptance criteria and training users in best practices. As a Factory Service Engineer, Generalist, you’ll be frontline support for all production needs. You will be working in a fast-paced and dynamic interdisciplinary laboratory environment, supporting stakeholders involved in adapting quickly to change and new technical challenges. With your help, we’ll keep our symphony of automated instruments humming in tune. etc. | 7/7/2020 |
| 10681 | Eton Bioscience Union, NJ Process Assistant BS/BA in life sciences Exp: 1 years in lab |
As a Part-time Process Assistant (M-F 7-11PM) you will be helping our lead lab technicians sorting samples, making measurements, calculating amount and dispensing micro fluid while logging electronic record. Previous experience working in a molecular biology lab setting is preferred but not required. If you are interested to work in the Bio/Pharma industry, this will be a good entry position. | 7/5/2020 |
| 10682 | Eton Bioscience Union, NJ Process Assistant BS/BA in life sciences Exp: 1 years in lab |
As a Part-time Process Assistant (M-F 7-11PM) you will be helping our lead lab technicians sorting samples, making measurements, calculating amount and dispensing micro fluid while logging electronic record. Previous experience working in a molecular biology lab setting is preferred but not required. If you are interested to work in the Bio/Pharma industry, this will be a good entry position. | 7/5/2020 |
| 10683 | Eurofins Austin, TX EMC Technician AA, technical school Exp: 0-2 years |
Responsible for setting up and executing, evaluating, and documenting tests. Conduct tests and all related tasks. Serve as lead engineer for projects assigned. Complete related tasks assigned by lab manager. | 7/5/2020 |
| 10684 | Eurofins West Point, PA Downstream Process Development Scientist BS/BA in life sciences Exp: 0-2 years in industry |
Perform lab-scale downstream processing of vaccine products and process intermediates. Perform assays on vaccine products, process intermediates, and related experimental samples using biochemical/analytical tests. Prepare solutions/reagents. Set-up process equipment for lab-scale experiments | 7/5/2020 |
| 10685 | Eurofins Piscataway, NJ Aesthetician-Clinical Research Coordinator BS/BA in sciences/healthcare Exp: 1-3 years |
Measure physical effects on the bodies of study subjects using high-end instrumentation. Manage Bioinstrumentation and related tests and documentation under the supervision of the manager/P.I. Maintain a professional, courteous and respectful work environment. | 7/5/2020 |
| 10686 | Eurofins Lee's Summit, MO Laboratory Technician BS/BA in sciences Exp: 1 year in lab |
The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results | 7/5/2020 |
| 10687 | Eurofins Austin, TX RF Test Engineer BS in electrical engineering Exp: 1 year RF testing |
Test common North American and European regulatory standards for licensed and unlicensed radio devices. Previous experience working in a commercial test laboratory a plus. EMC testing experience also a plus | 7/5/2020 |
| 10688 | Evonik Richmond, VA Richmond site ESH Associate BS/BA in ESH or science field Exp: 0-3 years in environmental, safety, or health |
The ESH Associate will serve as the site ESH Coordinator for the Richmond Business and Innovation Center. They will implement, monitor, and support environmental, safety, health and security programs and initiatives. They will ensure that the Business and Innovation Center is in compliance with the Responsible Care and ISO 14001 standards. They will work with facilities in the region to gain an understanding of plant chemistries and operations. They will assist with regional and segment projects as needed. | 7/5/2020 |
| 10689 | Evonik Mapleton, IL Chemical Operator Assistant HS Diploma/GED, vocational training preferred Exp: 1-3 years in industrial/chemical plant preferred |
Environmental, Health, Safety, Quality (EHSQ) Compliance. Process/equipment and areas of operating responsibility. Completes building equipment safety inspections. Monitors and coordinates building waste recovery and disposal activities. Inventories and orders designated building supplies. | 7/5/2020 |
| 10690 | Evonik Richmond, VA Richmond site ESH Associate BS/BA in ESH or science field Exp: 0-3 years in environmental, safety, or health |
The ESH Associate will serve as the site ESH Coordinator for the Richmond Business and Innovation Center. They will implement, monitor, and support environmental, safety, health and security programs and initiatives. They will ensure that the Business and Innovation Center is in compliance with the Responsible Care and ISO 14001 standards. They will work with facilities in the region to gain an understanding of plant chemistries and operations. They will assist with regional and segment projects as needed. | 7/5/2020 |
| 10691 | Exact Sciences Madison, WI Patient Financial Services Associate I HS Diploma/Ged Exp: 1 year in medical billing/claims |
The Patient Financial Services Associate I (PFSAI) position is responsible for the accurate and timely processing of claims, appeals, denials, and statements for Exact Sciences. A PFSAI demonstrates medical insurance knowledge by resolving billing discrepancies, eligibility, denials, appeals, and aged unpaid claim follow up for commercial, government, and plan coverage for optimal Account Receivable (AR) outcomes. | 7/5/2020 |
| 10692 | Exactech Gainesville, FL Associate Demand Supply Analyst BS/BA or better Exp: 0-1 years |
Utilize Supply Chain tools and systems to regularly monitor demand and supply exceptions and imbalances; takes necessary steps to prevent and/or correct anticipated supply/demand problems considering all alternatives and consequences of decisions. Schedule weekly discussions with Purchasing to review planned purchases/receipts, trade priorities with suppliers to meet customer needs and identify any purchasing gaps that would need to be resolved to ensure best possible purchased supply. | 7/5/2020 |
| 10693 | Exela Pharma Sciences Lenoir, NC Quality Assurance Operations Associate BS/BA in sciences Exp: 0-3 years in GMP industry |
The QA Operations team provides direct support for all manufacturing activities. This position supports the Quality Systems within the Quality Assurance Unit ensuring compliance with federal regulations for current Good Manufacturing Practice (cGMP) for finished pharmaceuticals. Review of batch records during active manufacturing. Perform routine manufacturing area line clearances | 7/5/2020 |
| 10694 | Exelixis Alameda, CA Vivarium Technician II BS/BA Exp: 1 year experience |
The successful and highly motivated candidate is responsible for animal husbandry and housekeeping of animal holding and support areas. The Vivarium Technician will assist and support the daily activities for the in vivo pharmacology program. Maintains animal husbandry and housekeeping of animal holding and support areas. | 7/5/2020 |
| 10695 | Exelixis Alameda, CA Temporary Assistant Research Scientist I (Compound Repository) BS/BA in related Exp: 1 year in related |
The candidate will be responsible for creating daily compound stock solutions to support creation of library screening plates. This job will require the candidate to have excellent organization, communication, and teamwork skills, as well as flexibility and versatility, to meet tight deadlines in a dynamic, fast-moving environment. | 7/5/2020 |
| 10696 | Exelixis Alameda, CA Assistant Research Scientist II (Pharmacology) MS in biological sciences Exp: 0-2 years |
Assist in the planning, design and implementation related to animal studies of pharmacokinetics, pharmacodynamics, and efficacy to evaluate and differentiate lead validation and lead optimization programs under general supervision. Compliance with IACUC protocols and AAALAC regulations in conducting general research duties within assigned area of responsibility | 7/5/2020 |
| 10697 | Biotechne Minneapolis, MN Quality Technician HS Diploma or Associates Exp: HS: 1-3 years, AS: 0-1 years |
The responsibilities of a Quality Technician are to assist in receiving and inspecting raw materials, intermediates and products used in scientific research. Duties may require document and product reconciliation, inventory management (electronic), and assisting with complaint investigations. Employees must have the ability to work independently and as a part of a team environment. | 7/5/2020 |
| 10698 | Biotechne Minneapolis, MN QA Specialist BS/BA in sciences Exp: 0-2 years in QA |
The responsibilities of this position are to support the Quality Assurance function within Bio-Techne through quality systems development, quality systems auditing, documentation review, and other QA functions. Assist in Quality review of newly written or revised GMP specifications, documents, labels and literature for accuracy and completeness. Write documents as needed. | 7/5/2020 |
| 10699 | Biotechne Minneapolis, MN Research Associate (Serological Assay) BS in biological sciences Exp: 0-2 years of related |
The responsibilities of this position are to perform ELISA assays to check for quality performance of product, maintain accurate documentation of results, and maintain assay databases. This position will focus on quality control testing of serological assays. This position may also contribute to quality control testing of Quantikine ELISAs, Luminex assays, and/or IVD kits. Perform raw material qualification testing as needed. Calculate data and compile results efficiently. Collaborate with others and perform general lab duties as needed. | 7/5/2020 |
| 10700 | Biotechne Minneapolis, MN Manufacturing Technician - Quality HS Diploma or Associates Exp: HS: 1-3 years, AS: 0-1 years |
The responsibilities of a Quality Technician are to assist in receiving and inspecting raw materials, intermediates and products used in scientific research. Duties may require document and product reconciliation, inventory management (electronic), and assisting with complaint investigations. Employees must have the ability to work independently and as a part of a team environment. | 7/5/2020 |
| 10701 | Biotechne Minneapolis, MN Research Associate (Protein Purification) BS in biochemistry or equivalent Exp: 0-2 years in chormatography |
The responsibilities of this position is to purify proteins for restock and modify existing protocols to meet the demand of our customers. This position will require assistance with basic lab operations and routine guidance on how to follow SOP’s and purification methods. | 7/5/2020 |
| 10702 | Biotechne Minneapolis, MN Production Assistant HS Diploma Exp: 0-2 years |
You will be responsible for assisting in the Clinical Controls Product Finishing Department with the bottling operation and the other activities involved in the product finishing process. Cap vials or tubes, operate the torqueing equipment. Label product, operate the labeling equipment. Assist with monthly cleaning of clean room, including counters, laminer hoods, torque, labeler, sinks, and all work areas. | 7/5/2020 |
| 10703 | Biotechne Minneapolis, MN Manufacturing Assistant HS Diploma/GED Exp: 0-2 years |
You will be responsible for assisting in the Clinical Controls Product Finishing Department with the bottling operation and the other activities involved in the product finishing process. Cap vials or tubes, operate the torqueing equipment. Assist department in maintaining inventory of vials, tubes, closures, Styrofoam trays and dividers. | 7/5/2020 |
| 10704 | Abcam Cambridge, MA Research Associate - Assay Development MS in bioengineering/biochemistry Exp: 1-2 years |
Perform mammalian cell culture including adherent, suspension cell lines and primary cells. Assist in developing and optimizing the protocols for cell based functional assays which includes potency assays and immunoassays. Clearly document experiments and procedures in laboratory notebooks, analyzing and presenting experimental data within internal team meetings. | 7/5/2020 |
| 10705 | Abcam Cambridge, MA Logistics Technician HS Diploma/GED Exp: 1-3 years |
Process incoming shipments from suppliers, ensuring accuracy of all product data. Aliquot product into vials and assemble kits for customer orders and global stocking. Work with colleagues across the business to resolve discrepancies quickly. Maintain accurate inventory levels using both manual and automated systems. | 7/5/2020 |
| 10706 | Abcam Milpitas, CA Cell Science Research Associate BS in cell biology or related Exp: 1 year in lab |
Perform cell engineering using CRISPR technology for service type cell-based projects. Generate and maintain modified cancer, iPSC and other cell lines in BSL-2 level laboratory environments. Generate high-quality and deliverable data, perform data analysis and report in a timely, troubleshooting wherever needed; Collaborate and exchange the technique protocols, tips and experience with other team members internally or externally | 7/5/2020 |
| 10707 | Exact Sciences Madison, WI Production Associate I Associates in life sciences Exp: 1 year in lab setting |
The Production Associate I is an entry level position and is the starting point to acquire skills and training required for the Exact Sciences Production Operations team. This role will participate in a variety of Production functions, which include bulk reagent production and dispensing, label application, and kitting of finished goods. The position will work within defined protocols and procedures with frequent supervision. | 7/5/2020 |
| 10708 | Exact Sciences Madison, WI Patient Access Associate I HS Diploma/Ged Exp: 3+ months in healthcare |
The Patient Access Associate I (PAAI) position is responsible for the accurate and timely filing of insurance claims for Exact Sciences. A PAAI demonstrates medical insurance knowledge by determining initial and/or ongoing eligibility and authorization of insurance including commercial, government, and plan coverage. PAAI communicates insurance information to ancillary departments and ensuring appropriate coverage by utilizing Epic, external portals, and other software. | 7/5/2020 |
| 10709 | Exagen Vista, CA Research Associate (Flow Cytometry) BS in biological sciences Exp: 0-1 years, experience in flow cytometry preferred |
The Research Associate assists with the development of new assays for diagnostics and research projects, through various phases of inception, planning and transfer to the clinical lab. Assist with the development, optimization and validation of new diagnostic assays. Perform all aspects of laboratory activities, for example sample preparation, staining, acquisition, and data analysis, with a focus on flow cytometry. | 7/5/2020 |
| 10710 | Genomenon Ann Arbor, MI Inside Sales Specialist BS Biology or Bioinformatics Exp: 0 yrs |
The successful candidate will provide commercial and inside sales support for the rest of the team including outbound prospecting, handling inbound leads, qualifying opportunities and connecting the prospects with the outside sales team. This person will have a basic understanding of molecular biology and NGS applications and the ability to engage with potential users of our software. | 7/2/2020 |
| 10711 | Sebela Pharmaceuticals Holbrook, MA QC Chemist BS in chemistry or related Exp: 0-2 years |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. PRINCIPAL DUTIES AND RESPONSIBILITIES: Perform testing of raw materials and products. Perform instrument qualification and maintenance. Perform test method validation/verification. Review analytical data for completeness, accuracy, and compliance. Perform training on procedures, equipment, or quality systems. etc. | 7/1/2020 |
| 10712 | Sebela Pharmaceuticals Holbrook, MA Production Worker HS diploma or equivalent Exp: 0-2 years |
Support Manufacturing and Packaging Operations under cGMP conditions. PRINCIPAL DUTIES AND RESPONSIBILITIES: Account for inventories and move material using pallet jacks. Weighing, metal detecting and blending of product. Set up equipment to run product to specification. Fill hoppers with raw materials. Load components (bottles, cartons, cups, booklets, shippers) onto machines. etc. | 7/1/2020 |
| 10713 | Senes Tech Phoenix, AZ Manufacturing Technician AS/AA in an electro-mechanical discipline Exp: 1-2 year(s) |
Would you welcome a highly responsible role at a revolutionary company? SenesTech, a platform life sciences company, is seeking a Manufacturing Technician to process and package finished goods, operate machines and take responsibility for facilities and planned maintenance. The key responsibilities of a Manufacturing Technician include, but are not limited to: Responsible for making ContraPest® according to SOPs and Batch Record instructions and takes responsibility for manufacturing a quality product. Performing set-up, dismantling, and maintenance of equipment and assuring that equipment is ready for production operations, performing routine sanitization of areas and equipment maintenance such as periodic equipment cleaning, inspection, and filter changes, etc. | 7/1/2020 |
| 10714 | Siemens Elgin, IL Assembler Associate - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
We are looking for dedicated people with the skills and vision to build a better tomorrow! By joining our manufacturing team, you will be under close supervision, and will be responsible for assembly of wind turbine repair kits! Your Responsibilities. Receive parts from stockroom, document serial numbers and other needed information. Check, skid, package, and tag part per BOM(Bill of Material). Assemble parts per engineering instructions and blueprints and assist in disassembly of gear boxes. Operate overhead crane and other equipment as required. etc. | 7/1/2020 |
| 10715 | Siemens Walpole, MA Laboratory Technician 2 - QC Systems Improvement BS in medical technology, immunology, biochemistry or related Exp: 1+ year(s) |
Join our team now at Siemens Healthineers as a Laboratory Technician 2. This position will be responsible for the implementation of the standardization strategy for each individual ADVIA Centaur and Atellica products and the installation of several complex testing instruments within a new lab space. This person will be a part of a small team focused on developing standardization strategies for existing products. This includes developing Anchor and Gold Standards and MDPs when not in existence. In addition, this position will focus on modification to the value assignment process to align with new control system requirements. The position will participate in the execution of the design of experiments. This person will perform material and process validations following written protocols, and help prepare validation and/or test results reports. This person will work with serum and other biological fluids of human and animal origin. etc. | 7/1/2020 |
| 10716 | Siemens Littleton, CO System Specialist I – Smart Buildings / Automation - Denver HS diploma/AS/AA Exp: 1+ year(s) |
Responsibilities: Network Technologies: Assist with data back-up from data servers and the creation of automated back-up procedures. Support troubleshooting and resolution of inconsistencies in the functions or sequence of operations. Assist with the set-up and configuration of PC workstations and user interfaces. Support the confirmation of proper network performance. Operational Testing, Verification, and Acceptance: Run routine reports to review system operation. Participate in final inspection and testing. Support customer acceptance. Assist with customer training on system operations. Complete and submit routine written reports. Provide plans and control system documents to engineering for as-built drawings. etc. | 7/1/2020 |
| 10717 | Siemens Shoreview, MN System Specialist – Smart Buildings/Automation – Level I HS diploma/AS/AA Exp: 1+ year(s) |
Responsibilities: Network Technologies: Assist with data back-up from data servers and the creation of automated back-up procedures. Support troubleshooting and resolution of inconsistencies in the functions or sequence of operations. Assist with the set-up and configuration of PC workstations and user interfaces. Support the confirmation of proper network performance. Operational Testing, Verification, and Acceptance: Run routine reports to review system operation. Participate in final inspection and testing. Support customer acceptance. Assist with customer training on system operations. Complete and submit routine written reports. Provide plans and control system documents to engineering for as-built drawings. etc. | 7/1/2020 |
| 10718 | Siemens Elgin, IL Assembler Associate - 1st Shift HS diploma or equivalent Exp: 1+ year(s) |
We are looking for dedicated people with the skills and vision to build a better tomorrow! By joining our manufacturing team, you will be under close supervision, and will be responsible for assembly of wind turbine repair kits! Your Responsibilities. Receive parts from stockroom, document serial numbers and other needed information. Check, skid, package, and tag part per BOM(Bill of Material). Assemble parts per engineering instructions and blueprints and assist in disassembly of gear boxes. Operate overhead crane and other equipment as required. etc. | 7/1/2020 |
| 10719 | Siemens Grand Prairie, TX Manufacturing Fabrication Supervisor - 2nd Shift (Entry Level) BS/BA Exp: 0-1+ year(s) |
Siemens Industry is looking for a Manufacturing Fabrication Supervisor - 2nd Shift for our Grand Prairie, TX facility the heart of the DFW Metroplex. Our growing team has over 700 employees that produce high-quality, engineered and make-to-order power distribution equipment. The Production Supervisor is the key driver of all daily production-related processes and the hub of information transfer between the hourly assembly workforce and Management, Engineering, Quality Control, Purchasing, and Planning. etc. | 7/1/2020 |
| 10720 | Siemens Mishawaka, IN Biochemist Scientist-Technical Operations BS in chemistry or related Exp: Recent graduates considered |
The successful candidate will participate in a wide variety of semi-complex technical assignments with respect to systematic troubleshooting and support of manufacturing and supplier issues for paper-based diagnostic tests. The incumbent will be responsible for conducting customer complaint investigations, maintaining the control charting process for production reagents as well as writing and executing validation plans. Other duties include participation in root-cause analysis efforts and aiding in identifying process/equipment improvements as well as other testing as directed. This person must be highly competent in bench-scale solution preparation and willing to learn specialized testing techniques. Must also be able to prepare, analyze, and present coherent data for review and summarize results in a technical report. etc. | 7/1/2020 |
| 10721 | Sigilon Cambridge, MA Assistant/Associate Engineer, Biomaterials BS/MS in biomaterials, engineering, biochemistry, or biology Exp: 1-2 year(s) |
Responsibilities: Perform proper sterile technique for tissue culture of primary cells and cell lines. Maintain and set up devices for biopolymer encapsulation systems. Perform established protocols for encapsulation of cells in novel biopolymer systems, cell-based functional assays, and associated biomaterial characterization assays. Work in a matrixed environment to make biomaterials for preclinical studies associated with all developmental cell therapy programs. Make observations, evaluate data, and interpret and document results in a well-maintained laboratory notebook. etc. | 7/1/2020 |
| 10722 | Sinclair Research Auxvasse, MO Quality Assurance Officer - Remote Work BA/BS Exp: Not necessary for BS/BA candidates |
The ideal candidate will be detail oriented and love to research information. As a Quality Assurance Officer it will be your job to ensure that our studies are conducting following all rules and regulations whether internal or external. As a QA Officer, you will be expected to not only know regulations regarding proper study conduct but to hold others accountable to them. You may spend the day at your desk reviewing final reports and researching regulations or you may go out in the field and audit the facility or witness studies first-hand to ensure proper procedures are being followed. etc. | 7/1/2020 |
| 10723 | Sinclair Research Auxvasse, MO Animal Caretaker HS diploma or equivalent Exp: No experience necessary |
The ideal candidate will have a passion for animal welfare and a great work ethic. Hard-working individuals looking for a great environment and a chance to make a difference will fit right in. Your primary role will be taking care of our animals and sanitizing their housing and our buildings. This may include caring for rats, mice, rabbits, dogs, cats, swine, or even cattle! There may be some heavy lifting and some dirty work involved but, if you love the idea of spending your day with animals, it's worth it to take care of our little heroes. etc. | 7/1/2020 |
| 10724 | Sinclair Research Auxvasse, MO Animal Technician HS diploma or equivalent Exp: No experience necessary |
The ideal candidate will be hard-working and ready to be hands on. In this role, you will have a chance to participate daily in our research by working closely with our study directors, senior technicians, and scientists in order to conduct studies. Animal Technicians begin by learning the basics of data collection and animal husbandry and have the chance to move up into high level Technician roles. This is an entry level position and a great place to start your career in research and see where you may end up! etc. | 7/1/2020 |
| 10725 | Smith & Nephew Memphis, TN Machinist HS diploma or equivalent Exp: 6+ months |
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Operates saws (band/cut-off) to produce quality parts based on provided specifications. Operates washers and rinse tanks. Performs simple CNC/manual mill and lathe setup/operations within product families to produce quality parts based on provided specifications. Operates manual and/or CNC mills and lathes to produce quality parts based on provided specifications. Cleans machines and remove chips. Performs basis preventative maintenance on machines. Performs routine dimensional and visual inspection of product per procedure, specification or print using basic measuring equipment (caliper, micrometer, scale, indicators, SPC equipment). etc. | 7/1/2020 |
| 10726 | Smith & Nephew Seattle, WA Field Logistics Associate 2 BS/BA Exp: Not necessary for BS/BA candidates |
Responsibilities: Utilizes OSC Operation Service Center software application or designated Software Application System to schedule and prepare instruments and implant kits for to facilitate Surgery Case Scheduled ensuring timeliness and accuracy. Maintain and manage scheduled surgery cases on a daily basis. Process all required order entry as required and directed. Perform all required OSC reporting to measure accuracy, utilization and validations. Maintain accurate and complete OSC Bill of Materials (BOMs) for all instrument and implant kits. Maintain appropriate stocking levels for shelf stock & OSC kits. Ensure First In/First out method is being performed for all products. Ensure no expired product in all warehouse areas. etc. | 7/1/2020 |
| 10727 | Smith & Nephew Memphis, TN Finisher II HS diploma or equivalent Exp: Entry level |
The Finisher II will perform finishing techniques such as buffing, polishing, grinding, deburring and etching on machine products. Achieve proper size, finish and quality following drawings and quality specifications. Performs routine visual inspection and also uses basic measuring equipment. etc. | 7/1/2020 |
| 10728 | Smith & Nephew Memphis, TN Finisher I HS diploma or equivalent Exp: 0-2 years |
The Finisher I will perform finishing techniques such as buffing, polishing, grinding, deburring, and etching on machine products. Achieve proper size, finish, and perform quality by following drawings and quality specifications. Performs routine visual inspection and uses basic measuring equipment. etc. | 7/1/2020 |
| 10729 | Smith & Nephew Memphis, TN MDR Packaging Engineer BS in packing engineering or science or related Exp: 1-2 year(s) |
Responsible for the review and remediation of existing technical files to ensure the Packaging requirements meet the EU MDR regulations. Working with general supervision from the Senior Packaging Engineer, designs and develops packaging components and packaging systems for new and existing medical device products and/or product lines (sterile and non-sterile). Significant opportunity for individual action. Reports to the MDR Work Stream Leader of Labeling Operations & Global Packaging Technology, via the Senior Packaging Engineer Lead. etc. | 7/1/2020 |
| 10730 | Smith & Nephew Mansfield, MA Instrument Finisher I HS diploma or equivalent Exp: No experience required |
This position requires a person to transform components from a machined state to a complete, finished product while working in a team environment. Must be able to comply with all governing rules including Smith & Nephew policies and procedures and adhere to safety and cleanliness practices in the workplace. This position works under close supervision. (2nd Shift) Responsibilities: Finish instruments, including but not limited to: Assemble instruments by means of basic finishing processes such as bending, fitting, grinding, sharpening, deburring, bead blasting, tumbling and basic blending and polishing. etc. | 7/1/2020 |
| 10731 | Smith & Nephew Louisville, KY Field Logistics Associate 2 BS/BA Exp: Not necessary for BS/BA candidates |
Summary: The OSC II Operation Service Center Specialist is the senior OSC who coordinates schedules, prepares and ensures delivery of instruments and implants sets for surgery. They are responsible for maintaining accurate records of products as they flow through the territory. Accountability of products missing from sets is critical to ensure proper billings. Good working knowledge of company products, operating systems and procedures is critical. This position provides guidance and training to the OSC I position to ensure all requirements are performed for the OSC position. etc. | 7/1/2020 |
| 10732 | Sorrento Therapeutics San Diego, CA Research Associate, CAR-T (2 Openings) BS/MS in immunology, molecular biology, or related Exp: 0-2 years |
The Research Associate will be responsible for the development and implementation of in vitro studies to support pre-clinical validation of CAR-T cellular therapies against cancer. This position requires knowledge and hands-on experience in cell culture, Flow cytometry and cell-based assays. Essential Duties and Responsibilities: Design and execute experiments for development of preclinical CAR-T therapies. Isolate, expand and manipulate T cells. Perform in vitro functional assays; measuring cellular activation, cytokine release, proliferation and killing. Characterize T cells by flow cytometry (FACS).Analyze and interpret experimental data and present findings to colleagues on a weekly basis. etc. | 7/1/2020 |
| 10733 | Sorrento Therapeutics San Diego, CA Quality Control Microbiology Associate BS in microbiology Exp: 1-2 year(s) |
This individual will contribute to providing microbiological support and testing of cGMP environments, as well as contribute to in-process, drug substance, and drug release testing. ESSENTIAL DUTIES AND RESPONSIBILITIES: Environmental monitoring of cGMP cleanrooms per FDA and USP guidelines. Sampling of utilities (i.e. water, clean compressed air). Input and manage environmental data. Conduct QC testing of raw materials and utility samples; QC tests include, but not limited to bioburden, endotoxin, total organic carbon, conductivity, osmolality, and pH. etc. | 7/1/2020 |
| 10734 | Sorrento Therapeutics San Diego, CA QA Specialist I AA/BS in a scientific discipline Exp: 1-2 year(s) |
The QA Specialist's responsibilities are divided into three primary functional areas: Raw Material Inspection and Release, Label Generation, and Document Control. Raw Material Inspection: Associate is responsible for inspecting in-coming raw materials, releasing raw materials, obtaining and submitting test samples to the appropriate contract laboratory, and coordination of receipt of test results. Label Generation: Associate is responsible for ordering label and ribbon stock, generating Master Label templates from approved label specifications, producing labels for specific product lots, ensuring labels are verified as correct and are released in time to meeting the manufacturing schedule. etc. | 7/1/2020 |
| 10735 | Sorrento Therapeutics San Diego, CA Materials Associate HS diploma or equivalent Exp: 1-2 year(s) |
The Materials Associate's responsibilities are divided into three primary functional areas: shipping and receiving, inventory accountability, and other duties. Shipping and Receiving: Primary responsibility are shipping and receiving domestic as well as international packages. Responsible for incoming inspection of all materials. Inventory Accountability: Create and maintain inventory records and forward to appropriate departments. Issue supplies, materials and equipment to workers and ensure that all corresponding paperwork is accurately managed. Perform physical inventory inspections to ensure 100% of inventory accuracy. etc. | 7/1/2020 |
| 10736 | Spark Therapeutics Philadelphia, PA Facilities Engineer/Specialist BS in engineering or related Exp: 1-2 year(s) |
The Facilities Specialist will troubleshoot, repair and maintain facilities that includes infrastructure, utilities and equipment while ensuring the systems’ safety, compliance and cGMP regulatory when applicable. Maintains the overall facilities integrity and functionality by following established Preventive Maintenance (PMs) procedures and actively participates in troubleshooting activities by submitting and performing adequate Work Orders (WOs). Participates in the development and/or revision of Standard Operating Procedures (SOPs) and follows it when performing any work in cGMP areas or when it is applicable. Responds to critical facility equipment issues to eliminate safety concerns and minimize operational downtime. When necessary, coordinates and executes internal and external request for repairs, service and maintenance to facilities and equipment. etc. | 7/1/2020 |
| 10737 | Staar Surgical Monrovia, CA Quality Engineer MS in science or engineering Exp: 1 year |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: Support site production, operations, and quality and R&D teams by addressing emergent issues that might arise due to the operation processes. Serve as the quality representative during any product or process investigation. Lead investigations including root cause analysis and health risk assessment of the identified product or process nonconformities. Prepare and execute validations, technical studies, test method validations and other studies / reports as required. This includes preparation of protocols, establishment of test methodology and acceptance criteria, training personnel, execution, data analysis, investigation, and writing final reports. Initiate and lead project teams on non-conformance investigations regarding component failures, finished goods failures, and product returns. This includes but is not limited to performing risk analysis, determining root cause and recommending corrective action. etc. | 7/1/2020 |
| 10738 | Staar Surgical Monrovia, CA Production Technician (CNC) HS diploma or equivalent Exp: 1-2 year(s) |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: 1. Thorough knowledge of all applicable SOP's: makes proper decisions in line with applicable SOPs and standards under normal conditions. 2. Perform highly technical tasks in support of manufacturing including equipment set-up and manufacturing of product, tool changes, sterilization processes, and filtration of material and calibration activities as assigned. 3. Troubleshoot issues on equipment and assist with preventative maintenance. 4. Edit equipment programs (as required). 5. Assist in revising procedures related to operation and preventative maintenance. 6. Support qualification activities (as required). etc. | 7/1/2020 |
| 10739 | Staar Surgical Monrovia, CA Production Operator I HS diploma or equivalent Exp: 1-2 year(s) |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: 1. Thorough knowledge and appropriate implementation of basic production functions. 2. Completes required production documentation accurately. 3. Consistently meets quality and productivity targets. 4. Appropriately follows company policies, rules, and regulations. 5. Be able to interact well with others and work in a team environment. 6. Maintain work area environment in a clean and orderly manner. 7. Operate production related equipment. etc. | 7/1/2020 |
| 10740 | Steripharma Syracuse, NY Warehouse Technician - 1st Shift HS diploma or equivalent Exp: 1+ year(s) |
This position is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. How you make a difference . . . you will . . . Load and or unload materials using proper methods and procedures for securing materials. Receive, select and prepare materials for relocation to end users. Ensure accuracy of shipments and supporting documentation, receiving incoming material and routing to appropriate area or personnel, filling work orders, packaging assemblies and receiving into finished goods, ensuring inventory transaction are accurately logged and overseeing cycle counts and reconciliation activities. etc. | 7/1/2020 |
| 10741 | Steripharma Syracuse, NY Production Maintenance Technician, 2nd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. How you make a difference . . . you will . . . Performs maintenance work, to include equipment repair and preventative maintenance work as required or assigned. Performs the repair and maintenance of APA area floors and walls. Completes work orders and projects as assigned, supporting each team member as directed. Provides guidance to maintenance technicians in the diagnosis of electrical circuits, control problems, mechanical issues, and other problems that might arise during production runs, or during shutdowns and repairs. etc. | 7/1/2020 |
| 10742 | Steripharma Syracuse, NY Vial Pack Technician - 2nd Shift, Pharma HS diploma or equivalent Exp: 1+ year(s) |
This position operates vial wash/packaging production equipment. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. How you make a difference . . . you will . . . Operates all assigned equipment appropriately and per established methods and procedures, to include set up, operation and cleaning of equipment and parts, confirming configurations are correct, checking for leaks or other abnormalities or anomalies, ensuring proper communication of any issues or problems immediately, complete operational documentation per SOP, and tagging/palletizing/placement of all returned and rejected items as needed and required. etc. | 7/1/2020 |
| 10743 | Steris Chicago, IL Sterile Processing Technician I HS diploma or equivalent Exp: 0-1 year(s) |
Provides on-site support for the reprocessing of surgical instruments and trays to contracted facilities in compliance with the Department of Health, TJC, OSHA, CDC, AAMI and AORN standards and facilities goals and policies. Position level will be determined by previous job related experience, performance and certification requirements. Duties: Operates all mechanical machinery; cart washers, instrument washers, steam sterilizers, low temp sterilizers, ultrasonic and drying cabinets, within sterile processing. Uses established policies and procedures to complete work assignments. Learns and trains in all areas of sterile processing including decontamination, cleaning, assembly, wrapping, sterilization, and storage processes within all set professional standards and regulations. etc. | 7/1/2020 |
| 10744 | Steris Maple Grove, MN Field Service Technician AS/BS in electronics, mechanics, or related Exp: 1+ year(s) |
At STERIS, our Field Service Technicians act as the face of our company by ensuring top-notch service for our customers. In this field-based, customer-facing role, you will travel to hospital and surgical facilities to maintain, troubleshoot, service, and provide calibration and installation support for steam sterilizers, medical equipment washers and other STERIS products as needed. In addition, you will be responsible for building positive relationships with customers and colleagues, as well as completing necessary administrative tasks. Transferable skills for this role include mechanical (large military/agricultural equipment, appliances or vehicles), plumbing, HVAC, electrical, building maintenance and other similar field service repair work. etc. | 7/1/2020 |
| 10745 | Steris Burnsville, MN Field Service Technician AS/BS in electronics, mechanics, or related Exp: 1+ year(s) |
At STERIS, our Field Service Technicians act as the face of our company by ensuring top-notch service for our customers. In this field-based, customer-facing role, you will travel to hospital and surgical facilities to maintain, troubleshoot, service, and provide calibration and installation support for steam sterilizers, medical equipment washers and other STERIS products as needed. In addition, you will be responsible for building positive relationships with customers and colleagues, as well as completing necessary administrative tasks. Transferable skills for this role include mechanical (large military/agricultural equipment, appliances or vehicles), plumbing, HVAC, electrical, building maintenance and other similar field service repair work. etc. | 7/1/2020 |
| 10746 | Steris Denver, CO Repair Technician HS diploma or equivalent Exp: 1-3 month(s) |
The primary role of the Repair Technician is to perform repairs on medical instrumentation. Technicians will be trained to become familiar with various types of surgical instruments and understand how to best maintain and repair them. Repairs are completed on a repair truck onsite at a hospital or surgery center. In addition to repair work, Technicians may work with a team including Sales Representatives and RCs (Repair Consultants/Managers) to identify and capitalize on revenue opportunities. Travel requirements may vary by location. etc. | 7/1/2020 |
| 10747 | Steris Chattanooga, TN Sterile Processing Technician HS diploma or equivalent Exp: 0-1 year(s) |
Provides on-site support for the reprocessing of surgical instruments and trays to contracted facilities in compliance with the Department of Health, TJC, OSHA, CDC, AAMI and AORN standards and facilities goals and policies. Position level will be determined by previous job related experience, performance and certification requirements. Duties: Operates all mechanical machinery; cart washers, instrument washers, steam sterilizers, low temp sterilizers, ultrasonic and drying cabinets, within sterile processing. Uses established policies and procedures to complete work assignments. Learns and trains in all areas of sterile processing including decontamination, cleaning, assembly, wrapping, sterilization, and storage processes within all set professional standards and regulations. etc. | 7/1/2020 |
| 10748 | Steris Abilene, TX Field Service Technician AS/BS in electronics, mechanics, or related Exp: 1+ year(s) |
At STERIS, our Field Service Technicians act as the face of our company by ensuring top-notch service for our customers. In this field-based, customer-facing role, you will travel to hospital and surgical facilities to maintain, troubleshoot, service, and provide calibration and installation support for steam sterilizers, medical equipment washers and other STERIS products as needed. In addition, you will be responsible for building positive relationships with customers and colleagues, as well as completing necessary administrative tasks. Transferable skills for this role include mechanical (large military/agricultural equipment, appliances or vehicles), plumbing, HVAC, electrical, building maintenance and other similar field service repair work. etc. | 7/1/2020 |
| 10749 | Silverback Therapeutics Seattle, WA Lab Operations Assistant HS diploma/AS/AA Exp: 1+ year(s) |
Silverback Therapeutics, a Seattle-based biopharmaceutical company, is seeking a Lab Operations Assistant to join our team. The successful candidate will support research laboratory operations by completing tasks related to laboratory equipment, stockroom supplies, facilities, and shipping/receiving. Essential Duties & Responsibilities: Promote and facilitate a clean and organized laboratory work area, ensuring the laboratory is well-stocked and functioning smoothly. etc. | 7/1/2020 |
| 10750 | Singota Solutions Bloomington, IN Material Handler HS diploma Exp: 0-1 year(s) |
General Description including Skills and Physical Activity Requirements: 1. Must be very customer focused to both internal employees and external clients. 2. Must be able to work within the FDA regulated environment per its specific requirements and those established by internal policy and standard operating procedures. 3. Computer experience necessary or willing to take internal courses to gain such information quickly. Ability to work with Microsoft Office (Outlook, Excel, Word) a plus. Experience using ERP or inventory systems is not required, but helpful. 4. Effectively work within the configuration and rule process set up within an ERP system and bar code scanning environment to accurately manage inventory throughout the business. etc. | 7/1/2020 |
| 10751 | DSG San Diego, CA Business Development - San Diego, CA BS/BA in life sciences, business or computer sciences Exp: 1-3 years project management |
The Business Development Manager is responsible for identifying new clients and for establishing and maintaining sales relationships. This candidate is also responsible for maintaining and strengthening relationships with existing clients. Place outbound calls to market to qualify and build relationships with contacts, and secure meetings. Educate prospects on the eCaseLink suite of products and services. | 6/28/2020 |
| 10752 | DynoSense San Jose, CA QA Engineer BS in computer sciences/engineering Exp: 0-2 years |
Estimate, plan, and coordinate testing activities. Develop test plan, test cases, test scenarios based on Users Stories and product’s design description to meet business requirements and technical specifications. Perform ad hoc, functional, integration, and regression testing | 6/28/2020 |
| 10753 | Element Biosciences San Diego, CA Research Associate/Associate Scientist, Assay Development BS or MS in chemical or biological sciences/engineering Exp: 0-3 years |
The scientist will be involved in the development of library prep biochemistries and reagents for our new NGS technologies. Ideal candidates will have hands-on lab experience, good organizational skills, display a can-do attitude and be flexible about their activities. Expect to be part of a highly energetic and collaborative team. | 6/28/2020 |
| 10754 | Merck KGaA St. Louis, MO Cloud Engineer HS Diploma/GED Exp: 1 year working with cloud providers |
ou will work closely with various teams to ensure efficient operations of daily activities and drive continuous improvement efforts of products and processes. Technologies you will be working with include but are not limited to, Google Cloud Platform, Amazon Web Services, Microsoft Azure, Kubernetes, Docker, Jenkins, Terraform & Ansible. | 6/28/2020 |
| 10755 | Merck KGaA Jaffrey, NH Process Engineer BS in electrical, chemical, or mechanical engineering Exp: 1+ year in FDA regulated manufacturing |
The Process Engineer will work in a dynamic environment supporting the manufacture and testing of high purity filters with a focus on quality, process control/improvements, electro-mechanical assembly and material handling. The successful candidate will be an enthusiastic team player with high energy and strong engineering skills. | 6/28/2020 |
| 10756 | Merck KGaA Rockland, MA Rebate Associate BS/BA in finance, accounting or other business degrees Exp: 0-1 years in accounting/finance |
The Rebate Associate is responsible for analyzing customer and product utilization data and other deliverables to inform stakeholders of market share performance and to alert Finance, Brand, Contracting and Forecasting Managers to issues that require revenue management attention. In addition, the Rebate Associate will prepare quarterly and/or monthly payment packages, per the applicable contract, providing detailed analyses and reports, and submit for review and approval up through the highest levels of EMD Serono Management. | 6/28/2020 |
| 10757 | Merck KGaA Rockville, MD Report Writer 1 BS in life sciences Exp: 1+ year in lab/pharma company |
The Report Writer is responsible for writing/editing technical products including study protocols and study reports for the wide variety of assays that are offered as part of our Toxicology Services organization. Report Writers require a broad understanding of writing/editing, as well as working knowledge of assays or tests required to characterize product or material safety. Report Writers should understand scientific observations and ensure that reports meet the generally accepted professional/industry standards. They will maintain an understanding of technological principles and applications of the organization’s services. | 6/28/2020 |
| 10758 | Merck KGaA Sheboygan Falls, WI Packaging Operator 1 HS Diploma/GED Exp: 6 months in chemistry |
Wearing of appropriate protective gear, (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protection equipment "PPE" to protect themselves from toxic or corrosive chemicals in the forms of liquids, solids, vapors or airborne particles. The work area may occasionally be wet, humid abnormally hot or cold. Siting, standing, walking, reaching above the shoulder, stooping, kneeling, twisting, crouching or crawling for long periods of time. | 6/28/2020 |
| 10759 | Merck KGaA Danvers, MA Supplier Quality Engineer BS in engineering or life scineces Exp: 1+ years in quality engineering/auditing |
A new opportunity has arisen to join the Danvers Mobius Operations organization as a Supplier Quality Engineer in the Quality Systems team. Along with our Senior Quality Engineer, you support the supplier quality management process. Travel to domestic and international supplier locations may be required, 5%. | 6/28/2020 |
| 10760 | Merck KGaA Madison, WI Associate Production Scientist BS in chemistry or life sciences Exp: 0-4 years in pharma |
The Associate Production Scientist is a critical role in the safe and efficient manufacturing of APIs according to cGMP requirements. Demonstrate proper lab safety practices, and work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines. Working in a team environment, and being an effective member of a project team (PD through Production) | 6/28/2020 |
| 10761 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry or chemical engineering Exp: 0-4 years in chemical production |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Safely perform operations to meet quality expectations. Ensure quality throughout the process. Assure you are adequately trained to perform tasks/assignments. | 6/28/2020 |
| 10762 | Emerald Cloud Lab South San Francisco, CA Laboratory Operator BS/BA in life sciences Exp: 1-3 years in life sciences lab |
As a Laboratory Operator II, you will be responsible for high fidelity execution of detailed protocols. Operators are relied on for the immediacy and reliability with which experiments are run on the ECL, so attention to detail is crucial. The Lab Ops team relentlessly clears the queue of customer experiments and keeps the robots in the labs running at all times, with a focus on exactness and increasing efficiency. The entire ECL facility is run in a systematic way, and the team purview encompasses all protocols that enable this, from maintenance and control of instruments to inventory intake. | 6/28/2020 |
| 10763 | Emerald Cloud Lab South San Francisco, CA Laboratory Operator BS/BA in life sciences Exp: 1-3 years in life sciences lab |
As a Laboratory Operator I, you will run essential maintenance protocols for the instruments and the laboratory. These protocols are critical to sustaining the high quality operation of the facilities and provide experience working in ECL’s unique, systematic lab environment with our integrated software tools. | 6/28/2020 |
| 10764 | Emergent Biosolutions Baltimore, MD Analyst I, QC Analytical - Fill Line 2nd Shift BS in chemistry Exp: 0-2 years in chemistry |
Perform WFI sampling and testing as per current protocol, or validation protocols to support the WFI system. Perform sampling of raw materials. Clean the laboratory glassware using dishwasher or manually washing, if necessary. Perform daily laboratory tasks, such as balance calibration checks, temperature chart monitoring, CSR duties, etc. | 6/28/2020 |
| 10765 | Emergent Biosolutions Baltimore, MD Manufacturing Associate BS/BA Exp: 0-1 years in manufacturing/lab work |
Responsible for preparing tubing, equipment, supplies, and other items associated with sterile filling processes. Work under general supervision of more experienced Technicians or Production Supervisor. Comply with cGMP regulations, adhere to EBSI policies, and adhere to EBSI SOP and Batch Record directions. Complete all necessary documentation in a manner that complies with Good Documentation Practices as tasks are performed | 6/28/2020 |
| 10766 | Emergent Biosolutions Baltimore, MD Assistant Technician, Inspection&Packaging HS Diploma/GED Exp: 0-2 years |
Adhere to the procedures and safe practices for movement of product and materials and accurately complete all applicable documentation. This applies to room temperature and cold storage loctions. Execute and document procedural steps in compliance with cGMP standards. Perform 100% visual inspection of product and classify rejected materials utilizing approved categories within required timelines (Qualification) | 6/28/2020 |
| 10767 | Emergent Biosolutions Baltimore, MD Assistant Tech, Packaging & Inspection HS Diploma/GED Exp: 0-2 years |
This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. This position is located in Baltimore, MD at our Bayview site. Adhere to the procedures and safe practices for movement of product and materials and accurately complete all applicable documentation. This applies to room temperature and cold storage loctions. | 6/28/2020 |
| 10768 | Emergent Biosolutions Baltimore, MD Manufacturing Associate (Upstream) HS Diploma, BS preferred Exp: 1 year in pharma GMP |
The Manufacturing Associate II position reports to Manager Manufacturing at Emergent Manufacturing Operations Baltimore (EMOB). Prior experience in GMP manufacturing and operation of GMP process equipment are prerequisites. Operates manufacturing equipment such as: incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in process testing equipment | 6/28/2020 |
| 10769 | Emergent Biosolutions Baltimore, MD Manufacturing Associate BS/BA Exp: 0-1 years in manufacturing/lab work |
Responsible for preparing tubing, equipment, supplies, and other items associated with sterile filling processes. Work under general supervision of more experienced Technicians or Production Supervisor. Comply with cGMP regulations, adhere to EBSI policies, and adhere to EBSI SOP and Batch Record directions | 6/28/2020 |
| 10770 | Emergent Biosolutions Baltimore, MD Assistant Technician, Inspection&Packaging HS Diploma/GED Exp: 0-2 years |
Adhere to the procedures and safe practices for movement of product and materials and accurately complete all applicable documentation. This applies to room temperature and cold storage loctions. Execute and document procedural steps in compliance with cGMP standards. Perform 100% visual inspection of product and classify rejected materials utilizing approved categories within required timelines (Qualification) | 6/28/2020 |
| 10771 | Enanta Pharmaceuticals Watertown, MA Associate Scientist, Drug Metabolism & Pharmacokinetics (DMPK) BS in biological sciences Exp: 0-2 years in lab |
The Associate Scientist will work with an experienced Ph. D. scientist to conduct drug permeability and liver / intestine / lung / kidney transporter studies in support of Enanta drug discovery programs. She/he will be an integral member of Enanta’s highly collaborative Pharmacology and DMPK/Bioanalysis Department focused on the discovery of novel therapeutics against liver and viral diseases including nonalcoholic steatohepatitis (NASH), primary biliary cholangitis (PBC), respiratory syncytial virus (RSV), and hepatitis B virus (HBV), etc. | 6/28/2020 |
| 10772 | envisaaagenics New York, NY Bioinformatics Analyst MS in bioinformatics or related Exp: 1-3 years with various programing languages/systems |
The candidate will be responsible for building pipelines and creating tools to manage large volumes of sequencing data and will assist with generating and assessing meta-data to support internal R&D efforts. The ideal candidate will have experience with analysis of large datasets, knowledge of tools and biological databases, SQL knowledge, strong programming skills and proficiency in parallel and cloud computing. | 6/28/2020 |
| 10773 | Enzo Farmingdale, NY Temporary Production Associate Associates or BS/BA in biological sciences Exp: 0-2 years in sciences/lab work |
This position is responsible for the timely and efficient scheduling and packaging of standard and custom products, and for providing support to other areas of manufacturing to ensure timely product delivery. Assist in all packaging and labeling operations for Manufacturing. Assist in cGMP material inspection and receiving raw materials for Manufacturing. | 6/28/2020 |
| 10774 | Epic Pharma Laurelton, NY Chemist BS/BA in chemistry or related Exp: 1 year as chemist or related |
Analytical research and development, including analytical method development for assay, related compounds, dissolution for raw materials, in-process and finished products. Carry out method transfer and method validation. Draft validation protocols and reports. Work with different formulation types including tablets, capsules, soft gels, topicals and suspensions. Provide formulation support for research and development where required. | 6/28/2020 |
| 10775 | Editas Medicine Cambridge, MA Cell Manufacturing Associate I BS in biological sciences Exp: 0-2 years in industry/academia |
The candidate will contribute as part of a dynamic team to the development of gene-editing based ex vivo cell therapies in multiple disease areas, including hematology and immune-oncology. In this role, the candidate will be responsible for culturing and editing cells for use in Phase I clinical trials and for the creation of cell banks in a GMP environment. | 6/28/2020 |
| 10776 | Enzo Farmingdale, NY Production Associate Associates or BS/BA in biological sciences Exp: 0-2 years in sciences/lab work |
This position is responsible for the timely and efficient scheduling and packaging of standard and custom products, and for providing support to other areas of manufacturing to ensure timely product delivery. Assist in all packaging and labeling operations for Manufacturing. Assist in cGMP material inspection and receiving raw materials for Manufacturing. | 6/28/2020 |
| 10777 | ERT Pittsburgh, PA Sales Associate BS/BA in business/marketing/communications Exp: 1-2 years in commercial sales |
Identify, research and recommend new products and services for on-going projects based on client recommendations/requests and competitive intelligence. Coordinate with the project management and business development teams to identify, recommend and schedule in-person client visits when appropriate. Communicate with clients regarding services, the customer experience, potential problems, etc. | 6/28/2020 |
| 10778 | Eargo San Jose, CA Electro-Acoustic Engineer MS in asoustics/electrical engineering Exp: 1-2 years in audio product development |
The Electro-Acoustic Engineer would be involved in design and engineering development of audio requirements and systems, and related verification and validation of those requirements and systems for Eargo hearing instruments. Measure and validate audio performance at a system & component level. Failure Analysis & Problem solving of Audio Quality, Electroacoustics and Digital Signal processing algorithmic issue pertaining to hearing aids | 6/28/2020 |
| 10779 | Element Biosciences San Diego, CA Research Associate/Associate Scientist – Chemistry Product Development BS or MS in chemical or biological sciences/engineering Exp: 1 year as research associate |
Work closely with senior scientific staff to execute reactions that involve multiple complex materials. Optimize chemistry protocols and develop standard operation procedures. Assist troubleshooting problems in experiments in terms of assay design, protocol, reagents and characterization of materials. Prepare reagents, buffers and calibration standards | 6/28/2020 |
| 10780 | Regenxbio Rockville, MD Clinical Research Associate (In House) AS/BS Exp: 1-2 year(s) |
The Clinical Research Associate (CRA) supports and coordinates the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs and acts as a pivotal point of contact for the clinical trial team. Under general supervision, the incumbent will assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. Although prior CRA experience is not essential, a working knowledge of the clinical trial process and associated regulations, responsibilities, and roles are required. etc. | 6/25/2020 |
| 10781 | Repare Therapeutics Montreal, QC Laboratory Technician – Biology BS/MS in biology or related Exp: 1+ year(s) |
RESPONSIBILITIES: Tissue culture facility management: biosafety cabinet and incubator maintenance, cell line expansion, mycoplasma testing, banking, and confirming loss-of-function or gain-of-function gene mutations by sequencing, qPCR, immunoblotting, and functional assays. Utilize CRISPR/Cas9 genome editing and other cell biology tools to generate and characterize cell line models. Aid in the execution CRISPR-enabled genome-wide SL screens with other scientists. Production and management of lentiviral stocks. Management of biology lab inventory (ordering, stocking, and organizing). etc. | 6/25/2020 |
| 10782 | Repligen Waltham, MA Manufacturing Associate II Biomanufacturing (2nd Shift) BS in a biological science Exp: Not necessary for BS candidates |
The successful candidate will play a key role in ensuring that the department’s production and quality goals are met. Applicants must have strong technical knowledge and problem solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. Experience working in a GMP/document controlled environment would be beneficial. Attention to detail, and the ability to work in a team environment are essential. Candidates must be willing and able to learn new manufacturing processes as the company grows and also to work overtime. etc. | 6/25/2020 |
| 10783 | Retrovirox San Diego, CA Entry-level Marketing Unspecified Exp: Entry level |
The company is seeking an entry-level marketing person available immediately. We are seeking a fast-pace individual with experience in internet-driven social network marketing strategies with focus on use of Linkedin and Twitter to generate leads. Candidates must be located in San Diego, CA. Experience in internet-based and email-based marketing strategies is needed. Experience with website design, WordPress, email marketing and design, and SEO strategies are a plus. Ideal candidate should have some scientific background to be able to understand and implement novel strategies, evaluate competition, customer’s needs, and the services provided by the Company. Compensation will be based on commissions generated from new revenue. etc. | 6/25/2020 |
| 10784 | Rubius Therapeutics Cambridge, MA Associate Engineer BS in biochemistry, bioengineering, pharmaceutical sciences or related Exp: 0-2 years |
We are seeking an Associate Engineer (contract) to support solution preparation and process support activities within the upstream and downstream process development of Red Cell Therapeutics at our Cambridge, MA location. This associate will perform tasks including preparation and characterization of raw material stock solutions, upstream media formulations, and downstream process buffers while also contributing significantly to the buildout of infrastructure, workflows, and procedures needed to ensure consistent delivery of solution requests and traceable documentation of all source materials. etc. | 6/25/2020 |
| 10785 | Rubius Therapeutics Cambridge, MA Associate Engineer, Upstream/Downstream Process Development BS in life sciences or engineering Exp: 0-2 years |
We are seeking an Associate Engineer in the Cell Product Development group, focused on upstream and downstream of bioprocessing for the cellular therapy. They will work directly with a team of scientists to optimize, scale-up, and characterize the novel cell therapy platform to increase productivity and/or advance the clinical pipeline. They will be involved in hands-on manipulation of ex vivo derived cells, and collection and logging of a variety of generated data sets. The right candidate will have experience in laboratory research either in industry or academic settings. etc. | 6/25/2020 |
| 10786 | SAMDI Tech Chicago, IL Research Assistant BS in biology, biochemistry, chemistry or related Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. Responsibilities include: Support preparation of reagents and materials for running biochemical assays. Assist in executing biochemical assays utilizing state of the art mass spectrometry. Integrate automated liquid handling and support compound management. etc. | 6/25/2020 |
| 10787 | SCA Pharma Little Rock, AR IV Compounding Technician HS diploma Exp: 1 year |
These critical Team Members prepare and admix sterile pharmaceutical products in a highly controlled, regulated environment. This Team Member will undergo stringent training program to become qualified to work in aseptic environment inside ISO 7 rooms and ISO 5 workspaces ensuring admixtures are completed properly per FDA and cGMP requirements. BE ADVISED THIS IS A 2ND SHIFT POSITION: 2PM - 11PM. etc. | 6/25/2020 |
| 10788 | SCA Pharma Little Rock, AR Quality Assurance Analyst BS Exp: 1+ year(s) |
The Quality Analyst is responsible for performing Quality Assurance (QA) oversight of GMP compounding activities at SCA Pharmaceuticals. The Quality Analyst assists system owners in performance of non-conformance investigations, executes CAPA’s as they pertain to the QA department and supports validation and technical change control activities. This position requires advanced understanding of site processes in order to write technical documents including engineering studies and standard operating procedures. The position is a non-management position. The individual occupying it is expected to be capable of working with minimal supervision. The Quality Assurance Analyst is expected to communicate well with fellow Quality Assurance employees as well as Operations and Pharmacy departments. etc. | 6/25/2020 |
| 10789 | SCA Pharma Little Rock, AR Quality Assurance Batch Release Specialist BS/BA Exp: Not necessary for BS/BA candidates |
This position is responsible for performing Quality Assurance (QA) oversight of GMP compounding activities at SCA Pharmaceuticals. This position performs the QA review of batch records for final products and intermediates, coordinates testing of samples with the QC department, and reviews and evaluates QC data to ensure that lots meet applicable cGMP requirements prior to release. This position is responsible for the generation and issuance of plant documentation including: Standard Operating Procedures (SOP’s), Trainings, and Change Controls at SCA Pharmaceuticals. etc. | 6/25/2020 |
| 10790 | Seattle Genetics Bothell, WA Research Associate III Bioanalytical MS in the biological sciences Exp: 1 year |
The Translational Sciences department is seeking a highly motivated and creative research associate to assist with critical reagent discovery and bioanalytical assay development. This work will support the advancement of multiple antibody-drug conjugate (ADC) and immuno-oncology biotherapeutics from late-stage research into clinical development. The successful candidate will have experience in standard and exploratory bioanalytical techniques that can be used to characterize the pharmacokinetics, pharmacology, biodistribution, and/or stability of antibody-based drugs. etc. | 6/25/2020 |
| 10791 | Seattle Genetics Bothell, WA Research Associate II Bioanalytical BS in the biological sciences Exp: 1+ year(s) |
The Translational Sciences department is seeking a highly motivated and creative research associate to assist with sample testing and bioanalytical assay development. This work will support the advancement of multiple antibody-drug conjugate (ADC) and immuno-oncology biotherapeutics from late-stage research into clinical development. The successful candidate will have experience in standard and exploratory bioanalytical techniques that can be used to characterize the pharmacokinetics, pharmacology, biodistribution, and/or stability of antibody-based drugs. etc. | 6/25/2020 |
| 10792 | Repligen Waltham, MA Manufacturing Associate I - OPUS BS Exp: 1-2 year(s) |
This position will function in Repligen's OPUS Column Packing groups. Cross training into other departments may be required based on the changing needs of the department. The successful candidate will play a key role in ensuring that the department's production and quality goals are met. Applicants must have strong technical knowledge and problem solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. Responsibilities: Experience working in a classified cleanroom, and knowledge of GMP/ISO/document controlled processes would be beneficial. Attention to detail, and the ability to work in a team environment are essential. Ability to read engineering drawings and be familiar with process control software is also highly desirable. etc. | 6/25/2020 |
| 10793 | Repligen Marlborough, MA QC Technician AS/AA in biology or other scientific field Exp: 0-2 years |
The QC Technician will report directly to the QC Supervisor and will be primarily responsible for performing in-process testing and data collection of flat sheet membrane and tangential flow filtration cassettes. The analytical equipment you will be using to support this position includes spectrophotometer, balance, pipette, pressure gauges, timers, and stirred cells. The successful candidate will actively follow Repligen ISO 9001 Quality Management System in support of the manufacturing processes and final product testing, including additional laboratory compliance as assigned by the QC Supervisor. etc. | 6/25/2020 |
| 10794 | Repligen Waltham, MA Manufacturing Associate II - OPUS 2nd shift HS diploma/BS/BA Exp: 1-2 year(s) |
This position will function in Repligen's OPUS Column Packing groups. Cross training into other departments may be required based on the changing needs of the department. The successful candidate will play a key role in ensuring that the department's production and quality goals are met. Applicants must have strong technical knowledge and problem solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. etc. | 6/25/2020 |
| 10795 | Repligen Marlborough, MA QC Technician - 2nd shift BS/BA in biology or related Exp: 0-2 years |
The QC Technician will be responsible for performing in-process testing and data collection of flat sheet membrane and tangential flow filtration cassettes. The analytical equipment you will be using to support this position includes spectrophotometer, balance, pipette, pressure gauges, timers, and stirred cells. The successful candidate will actively follow Repligen ISO 9001 Quality Management System in support of the manufacturing processes and final product testing, including additional laboratory compliance as assigned by the QC Supervisor. Training will be on the first shift for approximately 6-8 weeks prior to transitioning to second shift. etc. | 6/25/2020 |
| 10796 | Regeneron Rensselaer, NY Packaging Process Engineer BS/MS Exp: 0+ years |
The Fill Finish Engineer will serve as an expert for Packaging equipment and processes directly supporting the operations team. They will support equipment design and selection as well as process development activities. They will be hands-on, solving issues during technology transfer, cGMP start-up and routine manufacturing for Regeneron internal operations. This role will also support validation and training activities for syringe assembly and labeling, auto-injector assembly and cartoning and palletizing equipment and processes. etc. | 6/25/2020 |
| 10797 | Regeneron Tarrytown, NY R&D Associate - Cardiovascular In-Vivo Pharmacology BS/MS Exp: 0-2 years |
The Cardiovascular (CV) and Renal Therapeutic Focus Area is currently seeking an entry level R&D Associate to support in-vivo pharmacology studies.. Primary responsibilities will include animal dosing, routine animal procedures, and support for study takedowns across disease indications within the CV Therapeutic Focus Area. Job Duties: Animal husbandry, blood collection, tissue harvesting, basic rodent surgery. Calculate drug dosage and prepare dosing solutions. etc. | 6/25/2020 |
| 10798 | Regeneron Tarrytown, NY R&D Associate- Clinical Bioanalysis BS/MS Exp: 0-4 years |
Clinical Bioanalysis is looking for an R&D Associate to join the team. This individual will execute experiments under the direct supervision of a manager, perform routine technical tasks and begin to manage, organize, and interpret data more independently. An ideal candidate should possess a knowledge of the basic principles of immunoassays obtained through academic training and/or relevant industry experience. RESPONSIBILITIES: Train on manual and automated bioanalytical methods and execute methods to perform bioanalysis for clinical studies under supervision. Execute multiple plates within the same day. etc. | 6/25/2020 |
| 10799 | Philips Gainesville, FL Product Quality Inspection Technician AS/BS in engineering Exp: 1+ year(s) |
In this role, you have the opportunity to be a part of Philips Health Tech’s Quality Control team in Gainesville, FL. Along with your team, you will be responsible for product inspection to insure that it meets business obligations for product flow while remaining compliant. You will work as a skilled worker preforming a number of non-repetitive product quality inspections. You will operate relatively autonomous within procedures, methods and techniques. etc. | 6/25/2020 |
| 10800 | Precision Medical Group Frederick, MD Repair Technician & Facilities Maintenance - Laboratory & Cold Storage (Fridge) HS diploma or equivalent Exp: 0-1 year(s) |
Our Bio-repository facility (similar to a warehouse) is hiring an entry level technician! You will monitor and report on all environmental storage units, performing preventive maintenance, repairing refrigeration equipment and monitoring systems. What the day-to-day will look like (in accordance with standard operating procedures, SOPs): Inspection and Repair; refrigeration, lab equipment, central monitoring system and emergency generator. Perform weekly inspections of emergency generators. Performing all inspections of refrigeration equipment which consists of a 15 point inspection of critical systems, including; oil level, compressor operation, electrical demand, temperature sensor calibration, etc. Performing performance qualifications of all refrigeration equipment. Reviewing equipment failures and evaluating potential causes with little supervision. etc. | 6/24/2020 |
| 10801 | Precision Medical Group Indianapolis, IN Business Intelligence Analyst I - Pharma Analytics BS/BA Exp: 1-3 year(s) |
Business Intelligence Analysts (BIA I & II) play a meaningful role in achieving our team’s goal of exceeding customers’ expectations with leading edge data management and data-driven insights and applications. A Glimpse of What Your Day-to-day will look like: Design, develop and administer a system for self and others to evaluate appropriateness of data for analytic hypotheses and applications. Develop and direct a process to clean and integrate complex healthcare datasets in order to create the data foundation for further analytics, client applications, and the development of key client insights. Contribute client team meetings for client engagements and strategic projects requiring complex data management support. etc. | 6/24/2020 |
| 10802 | Progenity Ann Arbor, MI Molecular Technologist Extractions I BS in medical technology or a life science Exp: 6+ months |
The Molecular Technologist – Extraction I works independently but closely with other technical staff, leads, supervisors, and the department manager to perform routine extractions within the Progenity laboratory. The Molecular Technologist – Extraction I may be asked to participate and execute task in support of processes for clinical research or development projects as required within Progenity. This position reports to the Extractions Lead and Laboratory Manager. RESPONSIBILITIES: Enters data accurately into the Laboratory information system (LIS). Documents all quality control activities, instrument maintenance, and calibrations daily. Provides information to document incidents and corrective action according to established procedures. etc. | 6/24/2020 |
| 10803 | Prosciento San Diego, CA Lab Assistant HS diploma/BS in a science or health related field Exp: 3 months |
Participates in and assists in supporting the laboratory aspects of human clinical trials under the direction of the Laboratory Supervisor. Performs laboratory procedures while ensuring the integrity of the studies and the safety and well-being of human subjects. Performs duties in accordance with ProSciento’s values, policies, and procedures. Essential Duties and Responsibilities will include the following. Other duties may be assigned at the company’s sole discretion. Participates in day-to-day clinical and laboratory activities and procedures, ensuring efficient workflow, appropriate collection and management of research subjects’ laboratory samples, and adequate care and treatment of research subjects, maintaining quality control of specimen samples. etc. | 6/24/2020 |
| 10804 | Prosciento San Diego, CA Business Development Associate BS/BA Exp: 1-2 year(s) |
The Business Development Associate (BDA) works directly with Business Development Directors to increase new account penetration to increase face-to-face meetings and Request for Proposals (RFP). The BDA supports Business Development Directors through research and analysis of industry trends and potential client pipelines through numerous data platforms to develop strategic sales leads. Performs duties in accordance with ProSciento’s values, policies, and procedures. Develops an in-depth knowledge about the scientific and operational benefits of ProSciento services to support Business Development Directors’ communication with perspective clients. Researches and analyzes industry trends and prospective client pipelines across numerous data platforms to generate strategic sales leads for new and ongoing clients for follow-up by Business Development Directors. etc. | 6/24/2020 |
| 10805 | Proteintech Rosemont, IL Scientist I; Cell Biology BS in molecular biology, cell biology, biochemistry, or related Exp: New graduates |
We are seeking a researcher to join a team focused on the expression and purification of human expressed proteins. The successful candidate will support the development and optimization of processes that produce cytokines and growth factors. These proteins will be used in cell therapy and stem cell research. Key Responsibilities: Maintain various cell lines for multiple projects. Expand cell lines for production. Work in a team environment with senior scientists and production scientists. etc. | 6/24/2020 |
| 10806 | Purdue Wilson, NC Pharmaceutical Technician, Packaging (2nd Shift: M-Th 4pm-2:30am) HS diploma or equivalent Exp: 1-5 year(s) |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Primary Responsibilities: Follow Master Batch Records for the packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. Identify, report, and resolve quality issues. Safely and in compliance with batch records and SOPs, set up, operate, and clean packaging equipment. Perform in-process testing and inspections as required by Master Batch Record. Clean and sanitize packaging rooms including walls, floors, and ceilings per SOPs. etc. | 6/24/2020 |
| 10807 | Purigen Pleasanton, CA Research Associate I/II BS in molecular biology, biology, biochemistry, or related Exp: 1-3 year(s) |
Purigen Biosystems, Inc., a Venture-backed, life science tools start-up company in the San Francisco bay area, is seeking an experienced Research Associate to join our Operations team. The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. This is a hands-on position for the highly qualified, self-motivated candidate who wants to enable cutting-edge life sciences technologies in a fast-paced, start-up environment. RESPONSIBILITIES: Set up and maintain mammalian cell line cultures and prepare cell samples by harvesting, cell-counting and lysing cells. Execute new and standard protocols for performance testing of Purigen’s custom Sample Preparation platform, including instrumentation and microfluidic chip prototypes. Set-up and execute bioanalytical QC assays, including qPCR, RT-qPCR, fragment sizing (e.g. Bioanalyzer assays) and nucleic acid quantitation assays (e.g. Nanodrop, Qubit). etc. | 6/24/2020 |
| 10808 | QIAGEN Germantown, MD Technical Assoc. Kit Assembly HS diploma/AS/AA Exp: 1-3 year(s) |
The Technical Associate Kit Assembly operations must comprehend and perform assigned automated and manual production tasks according to established Standard Operating Procedures (SOP’s). Responsible for Automated and/or Manual production and assembly procedures in compliance with relevant regulations and SOP’s. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of automated production equipment, as well as other production related equipment within the assembly area. etc. | 6/24/2020 |
| 10809 | QIAGEN Germantown, MD Technical Associate, Vialing and Assembly - 3rd shift HS diploma/AS/AA Exp: 1-3 year(s) |
The Technical Associate in Vialing and Assembly comprehends and performs assigned manual vialing of components under general supervision as well as using automation (large and small scale) in the production of finished product. Responsible for manual and automated production and packaging procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment. etc. | 6/24/2020 |
| 10810 | QIAGEN Germantown, MD Technical Associate Kit Assembly/Label printing HS diploma/AS/AA Exp: 1-3 year(s) |
Position Description: Must comprehend and perform assigned manual and automated kit assembly production tasks per established standard operating procedures (SOP). Support the label printing area printing labels as needed. Use computers, label printing and counting equipment to print / verify labels and perform all labeling related duties. Operate, maintain, and troubleshoot automated label printing and counting equipment. Operate, maintain, set up and trouble shoot manual manufacturing assembly equipment as described by production area SOPs. etc. | 6/24/2020 |
| 10811 | QIAGEN Germantown, MD Technical Associate Kit Assembly - 3rd shift HS diploma/AS/AA Exp: 1-3 year(s) |
The Technical Associate in Kit Assembly 3rdshift comprehends and performs assigned manual assembly / production tasks according to established Standard Operating Procedures (SOPs). Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. Responsible for maintaining product quality. etc. | 6/24/2020 |
| 10812 | QIAGEN Germantown, MD Technical Associate EZ1 Cartridge Manufacturing HS diploma/AS/AA Exp: 1-3 year(s) |
The Technical Associate in EZ1 Manual Filling/Assembly comprehends and performs assigned manual vialing of components under general supervision as well as using automation in the production of finished product. Responsible for manual and automated production and packaging procedures in compliance with relevant regulations and Standard Operation Procedures. Potential, for additional responsibilities with buffer production, weighing and addition of raw materials. Adhere to and accurately complete all production-related documentation. etc. | 6/24/2020 |
| 10813 | QIAGEN Germantown, MD Research Associate BS in biochemistry, molecular biology or related Exp: 1-3 year(s) |
The Research Associate will develop and evaluate innovative enzymes and enzyme mixes to be commercialized for use in molecular diagnostics, genomics, life science and related areas. The required tasks include construction, expression, screening and testing of commercially competitive enzymes. This position requires the ability to design and follow protocols, perform literature research, project plan, document and present results to groups of researchers. Duties include overexpression, screening, and biochemical characterization of novel enzymes and enzyme variants. Enzyme assay and/or applications development may also be required. etc. | 6/24/2020 |
| 10814 | QIAGEN Germantown, MD Protein Purification Technician I BS/BA Exp: 1-2 year(s) |
The Protein Purification Technician I performs assigned manufacturing and process development duties in a ISO 13485 environment. Job performance will involve a variety of activities including: Execute development and production scale purification protocols as directed. Work with standard scientific equipment as described in relevant procedures; AKTA Purifier and AKTA Pilot, UV spectrophotometer, balances, chromatography columns, SDS-PAGE, autoclaves, pH meter, refrigerators, freezers, biohazard safety cabinets. etc. | 6/24/2020 |
| 10815 | Quidel San Diego, CA Quality Control Instrument Technician BS in engineering Exp: 1-3 year(s) |
The Quality Control Instrument Technician is responsible for evaluating customer returned Sofia instruments and in-house Sofia instruments and assisting in complaint investigations. This individual is responsible for performing instrument triage and problem diagnosis. This individual will support commercialization of the Sofia instrument by providing technical support for customers, determining the failure mode for instrument complaints, and determining whether instrument problems are covered by manufacturer warranty, necessitating return to manufacturer. Analysis of field issues will also be used as feedback to R&D/Engineering for potential instrument upgrades or product improvements (hardware, firmware, software). etc. | 6/24/2020 |
| 10816 | Quidel San Diego, CA Associate Quality Engineer BS in engineering, chemistry, biology, or related Exp: 1-2 year(s) |
The Associate Quality Engineer is responsible for owning and coordinating Quality Engineering functions and activities for the defined processes. This position is also responsible for supporting the Production, Quality Control, Engineering and Quality Assurance departments and the associated activities, which include receiving inspection, in-process inspection, and finished goods inspection in achieving and exceeding company goals and objectives. In addition, this role is responsible for supporting the administration, implementation, and continuous improvement of the quality systems associated with non-conforming materials, inspection control plans, and corrective/preventive action. The Associate Quality Engineer supports corporate strategic goals and objectives through internal audits, support of manufacturing operations, product and process improvement projects, product qualifications and failure investigations for product complaints. etc. | 6/24/2020 |
| 10817 | Quidel San Diego, CA Accounting Associate II (Accounts Payable) HS diploma/AS/AA Exp: 1 year |
Quidel is searching for an Accounting Associate II to direct efforts of the Accounts Payable functions, and ensures transactions are completed timely and accurately. Reviews and maintains company accounts payable and receivable. Identifies and resolves customer/vendor disputes or discrepancies in a timely manner. Identifies IS support requirements. Exhibits an understanding of other organizations’ goals. Carries out duties in compliance with established business policies. ESSENTIAL FUNCTIONS: Processes payments to vendors and/or payments from customers. Maintains and reconciles customer and/or vendor accounts. etc. | 6/24/2020 |
| 10818 | Promega Madison, WI Refrigeration / Maintenance Technician 2 AS/AA Exp: 1+ year(s) |
Perform grounds duties, equipment installation, building upkeep, repairs and preventative maintenance. Requiring knowledge of plumbing, electrical, refrigeration, HVAC, building automation systems, and carpentry. Uses experience and judgment to plan and accomplish a variety of complicated tasks. A wide degree of creativity and latitude is expected. ESSENTIAL DUTIES: 1. Perform a wide variety of general building and equipment installation, modification, repair work and preventative maintenance. This includes, but is not limited to electrical, plumbing, drywall, painting, carpentry, floor repair and other general building, varied equipment and systems work. 2. Perform HVAC, boiler, compressed air, refrigeration and other building systems trouble shooting. Identify and recommend the most effective, efficient, and timely course of repair action. etc. | 6/24/2020 |
| 10819 | Promega Madison, WI Product Finishing IVD Technician - 1st & 3rd Shift (6 month project position) HS diploma or equivalent Exp: 1+ year(s) |
JOB OBJECTIVE: Technician with a full understanding of the department including dispensing, kitting and labels. Uses technical concepts and depth of knowledge to resolve issues effectively. ESSENTIAL DUTIES: 1. Setup, operate and maintain manual and automated dispensing, capping and labeling equipment. 2. Pull products from inventory and assemble components into kits and kit sub-assemblies using quality system documents, including kit packaging diagrams (KPDs). 3. Accurately complete all required written documentation for batch records. etc. | 6/24/2020 |
| 10820 | Discovery Life Sciences Huntsville, AL Laboratory Associate - Cell Processing BS/Ba in biological sciences Exp: 1-3 years lab experience |
To be successful in this job you must be detail oriented, analytical, methodical, responsible, team focused and enjoy learning. You must also have a working knowledge of universal precautions, bloodborne pathogens and handling human biospecimens, proven laboratory experience including basic mammalian cell culture techniques, knowledge of aseptic techniques and excellent computer skills. | 6/21/2020 |
| 10821 | Discovery Life Sciences Huntsville, AL Feasibility Associate BS/BA in life sciences Exp: 0-2 years, research preferred |
The individual in this position must keep abreast of oncologic and immunologic diseases. Are you someone with a strong life sciences background who is analytical, decisive, detail-oriented, and an excellent communicator who's looking for a future with a growing biotech company? To be successful in this role, you must have a Bachelor's degree, preferably in life sciences. You must be able to multitask, maintain organized records, efficiently manage several projects simultaneously, think outside of the box and develop creative solutions to problems. | 6/21/2020 |
| 10822 | Discovery Life Sciences Huntsville, AL Clinical Data Associate BS/BA in life sciences Exp: 0-2 years in biotech |
To be successful in this role, you must be curious, analytical, detail-oriented, love heavy computer work, and be a team player. A Bachelor's degree, preferably with a major in life sciences is preferred. Previous biotech or medical experience is also preferred. | 6/21/2020 |
| 10823 | Discovery Life Sciences Huntsville, AL Project Support Associate Associates or BS in related Exp: 1-2 years in admin/customer service |
We're looking for two (2) standout Project Support Associates who will manage our off-the-shelf inventory projects and provide excellent support to a team of Project Managers, allowing them to remain focused on fulfilling customer expectations. To be successful in this role, you must be highly organized, detail-oriented, be familiar with medical and pathology terminology, have great computer skills, be an excellent communicator and team player. | 6/21/2020 |
| 10824 | Distributed Bio South San Francisco, CA Project Manager BS/BA or MS in biological sciences/engineering Exp: 1-4 years related experience |
Project managers coordinate between our clients, our project leads, our senior project management and director of contract research. They act as the advocate for the client to the team and the advocate of the team to the client.Project managers become experts in all of our discovery technologies, and communicate the status of projects to clients as they progress. | 6/21/2020 |
| 10825 | DNA Diagnostics Center Boston, MA Specialist, Specimen Collection HS Diploma/GED Exp: 1-2 years in customer service/call center |
This position reports to the Satellite Office Supervisor and is essential to support our local customer base. This individual will perform DNA buccal swab and blood collections locally and forward the sample to DDC headquarters in Ohio for testing. This individual will run the day-to-day operations of the office independently. | 6/21/2020 |
| 10826 | Cytek Biosciences Fremont, CA Research Assistant - Flow Cytometry - Reagent Development BS/BA in chemical/biological sciences Exp: No experience required |
This individual will work with other scientists in the group to identify and evaluate antibodies and fluorescent dyes for developing flow cytometry reagents. Conduct immunological conjugation with different antibodies and fluorophores. Perform routine analysis of reagent using chromatographic spectrophotometer, HPLC and flow cytometry technique. | 6/20/2020 |
| 10827 | Cytel Indianapolis, IN Project Assistant BS/Bsc/BA Exp: 1-3 years in project management preferred |
The Project Assistant will primarily interface with Cytel project staff but may be required to communicate regularly or ad hoc with Sponsors ( e.g. in order to report status for timelines, scope and budget) or with DMC members (e.g. to schedule DMC meetings, deliver DMC reports, etc).Manage core project documents for timelines, scope, budget, and team lists. Track timelines and budget performance, and report status to Project Management | 6/20/2020 |
| 10828 | Cytomx Therapeutics South San Francisco, CA TEMP Protein Expression, Protein Sciences MS in biochemistry or related Exp: 1 year ini biotech/pharma |
We seek a highly motivated individual to participate in the expression and purification of protein reagents to support all discovery and development programs at CytomX. The successful candidate will work as a Temp up to 12 months in the Protein Sciences department. Conduct QC testing of DNAs that goes into transfection. Support the protein production by small and large scale transient transfection of CHO and 293 cells | 6/20/2020 |
| 10829 | Cytovance Biologics Oklahoma City, OK ANALYTICAL DEVELOPMENT ASSOCIATE BS or MS in life sciences Exp: 1 year in direct epxeriences |
The AD Associate I/II position develops, optimizes, and qualifies analytical methods for biopharmaceutical products. The associate also supports drug development departments, such as Purification Department and Cell Culture Department, by performing analytical testing. Develop analytical test procedures on biopharmaceutical products including: potency testing, SEC-HPLC, RP-HPLC, cIEX, Affinity Chromatography, SDS-PAGE, ELISA, IEF. | 6/20/2020 |
| 10830 | Cytovance Biologics Oklahoma City, OK DOWNSTREAM MANUFACTURING ASSOCIATE Associates in science/engineering Exp: 0-2 years in GMP production |
This position is accountable for the execution of procedures for purification manufacturing and support area of manufacturing using SOP’s and batch records. Operating production equipment for purification that may include process monitoring, purification and formulation. Interface with Quality Control department to submit in-process samples and coordinate environmental monitoring during key process steps. | 6/20/2020 |
| 10831 | DayZero Diagnostics Boston, MA Research Lab Associate Position BS/Ba in biological sciences Exp: 1 year in lab experience |
Perform and assist with molecular biology and microbiology experiments to support diagnostic development. Work closely with other Research Scientists and Associates to design and execute experiments. Ensure timely and accurate data outputs. Receive and process clinical specimens from submitting laboratories. Ensure quality control of equipment, reagents, and clinical samples. | 6/20/2020 |
| 10832 | DayZero Diagnostics Boston, MA Bioinformatics Engineer Position BS or MS in computer science/informatics/computational biology Exp: 1-3 years, fluency with Python, lynux, SQL |
In this role, you will work within the Comp Bio Team to develop, operate and optimize microbial genomics pipelines and their surrounding software infrastructure. We are looking for candidates who are as passionate about software development as they are about building high-quality data products. Tools and analyses will be used to advance internal R&D projects as well as to serve customer-facing products. | 6/20/2020 |
| 10833 | Decipher Biosciences Vancouver, BC Data Scientist & Data Engineer MS in data sciences/bioinformatics Exp: 1+ years in data sciences/cloud platforms |
As a data scientist, you will work closely with a team of research and production professionals. You will be a key member in preparing, interpreting and analyzing business, genomic and clinical data, providing analysis support to our colleagues and our external partners. Perform data analysis that contributes to the process improvement of Decipher products. | 6/20/2020 |
| 10834 | DeepBiome Kendall Square, MA Research Associate MS or BS in bioengineering or other life sciences Exp: 1-2 years in lab |
Types of activities include plasmid construction and preparation, transformation and culturing, plus preparing experimental media and buffers. Responsible for design, assembly, manipulation and cloning of DNA constructs for in vivo bacterial expression. Construct gene and pathway plasmid constructs using assembly methods such as: yeast homologous recombination, Gibson assembly, Golden Gate assembly. | 6/20/2020 |
| 10835 | Denison Acquisition Lincoln, RI Compounder HS Diploma/GED Exp: 1 year in similar job/industry |
Submitting a requisition for raw materials. Verifying the clean status of all equipment and utensils prior to use. Batch pre-staging operations. Weighing and blending raw materials. Following manufacturing instructions. Documents production by completing forms, reports, logs, and records of equipment and batches. | 6/20/2020 |
| 10836 | Denison Acquisition Lincoln, RI Warehouse Worker HS Diploma/GED Exp: 1+ years in manufacturing |
Receive components and chemicals,verify the acceptable condition of the containers prior to receiving the material, examine contents and compare with records such as manifests, packing slips, or invoices to verify accuracy of incoming shipments. Record the receipt of material into company ERP system | 6/20/2020 |
| 10837 | DermTech San Diego, CA Lab Technician or Research Associate: San Diego BS/BA or higher in life sciences Exp: 1-2 years in lab |
Conduct molecular diagnostic product development tests under direct supervision. Perform biological sample nucleic acid extraction, RT-qPCR and data analysis. Interact with team members to prioritize requests and deadlines | 6/20/2020 |
| 10838 | DermTech San Diego, CA Clinical Laboratory Scientist: San Diego BS/BA in sciences Exp: 1-2 years in lab |
The successful candidate will ensure that complex molecular diagnostic assays and systems are performed under appropriate CLIA compliance and regulatory requirements. The Clinical Laboratory Scientist independently performs clinical lab testing and other scientific examinations, record appropriate test documentations, and evaluates test results. | 6/20/2020 |
| 10839 | Dexcom San Diego, CA Engineering Technician 3 BS/BA Exp: 1-3 years lab/manufacturing experience |
As a member of the Sensor Research and Development team, the Lab Technician will work closely with Scientists and Engineers to manufacture next-generation sensors and support laboratory activities. Perform a wide variety of research and development laboratory tasks and experiments. Check standard laboratory supply inventory to assure adequate inventory levels and proactively place orders when running low. | 6/20/2020 |
| 10840 | Dexcom San Diego, CA Engineering Technician 1 HS Diploma/GED Exp: 1-2 years technical/mechanical experience |
In this role, the Technician will work alongside Engineers in order to assist in the development of products, processes, and root cause investigational efforts. The primary role being testing. The Technician will conduct measurements or tests following defined procedures. The test results will be used to determine product functional attributes, test fixture or test method design attributes, and assembly process variation. | 6/20/2020 |
| 10841 | Dexcom Charlottesville, NC SW Development Engineer 1 BS/BA in technical discipline Exp: 0-2 years |
You'll roll up your sleeves and tackle challenges as diverse as developing best-in-class apps under regulated regimes like HIPAA and FDA’s QMS, stringent cybersecurity requirements, all-in agile process (not SCRUMbutt), difficult and fluid end-user engagement problems, hacking locked-down IoT APIs, user experience design, back-end scalability, and business decision support. | 6/20/2020 |
| 10842 | Diacarta Richmond, CA Customer Service & Technical Support Specialist BS or MS in biology or related Exp: 1-3 years in life science companay preferred |
The customer service & technical support candidate will have strong technical knowledge in molecular biology and cancer diagnostics and will demonstrate technical credibility to effectively consult with customers and internal stake holders. Day to day responsibilities will include, sales order processing, order entry/dispatching/invoicing/post sales inquiries/responding to technical inquiries and trouble shooting. In addition, you will be responsible for dealing with general customer inquiries from new and existing customers, handling incoming leads from our website and update/maintain the lead tracking database. | 6/20/2020 |
| 10843 | Diacarta Richmond, CA Inside Sales Specialist BS in biology Exp: 1-3 years in biotech/industry |
The Inside Sales Specialist manages the customer sales process for specific products lines, accounts and/or sales opportunities via phone and e-mail. Includes engaging with existing customers and qualified sales leads, guiding customers to the DiaCarta products that best meet their needs, coordinating with internal resources to address customer questions/objections, providing budgetary pricing, creating and submitting individualized quotes and closing the sales process through the point of order receipt. | 6/20/2020 |
| 10844 | Digirad Mankato, MN Technologist Assistant HS Diploma/GED Exp: 1 month training, CPR certified |
Assisting the technologist with patient care by transporting patients between the facility and scanner; sanitizing and cleaning patient care and staff areas; changing table linens; entering exam and patient information electronically or on paper; and answering the telephone. Demostrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. | 6/20/2020 |
| 10845 | Digirad Houston, TX Nuclear Medicine Technologist Degree or certification in nuclear medicine Exp: 1 year in preforming imaging |
The Nuclear Medicine Technologist will work will work under the direct supervision of site physician, performing various duties related to nuclear stress testing. Performs patient care functions related to perfusion imaging and stress testing at customer sites. Perform functional and/or perfusion rest and stress cardiac studies, including processing images for physician review. | 6/20/2020 |
| 10846 | Digirad Novi, MI Cardiac Stress Technician Associates or BS in related Exp: Some experience in medical field/ emergency care preferred |
The Cardiac Stress Technician will work under the direct supervision of site physician, performing various professional and administrative duties related to nuclear medicine stress testing. This includes but not limited to patient preparation, administration of exercise and pharmacological stress tests, and application of ACLS measures to patients when directed. | 6/20/2020 |
| 10847 | GiscGenitcs Salt Lake City, UT Quality Engineer BS/BA in sciences/engineering/biotechnology Exp: 1 year in quality engineering |
Serves as the voice of quality during the product design and development process. Facilitates risk assessment activities. Defines and implements the Quality Management System processes in accordance with 21 CFR 210/211, 21 CFR 820, 21 CFR 1271, including CAPA, training, internal audits, supplier controls, etc. Leverages industry expertise and experience to guide and mentor company personnel through GMP/QMS requirements. | 6/20/2020 |
| 10848 | Decipher Biosciences San Diego, CA Sample Processor I BS in life sciences Exp: Entry Level |
The Sample Processor’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. | 6/20/2020 |
| 10849 | Pace Analytical Fargo, ND Lab Analyst - GMP Micro (Q3/Q4) BS in biotechnology, microbiology, or related Exp: 1 year |
The Microbiologist will work daily within labs performing tasks associated with GMP services. The Microbiologist is expected to become familiar with all of the products and to be able to perform most tasks associated with the purification of plasmid DNA. Note: We expect to hire for this position in Q3 or Q4 of 2020. RESPONSIBILITIES: Segregation, line clearance, and cleaning of GMP production areas. Planning and submitting inventory requisitions. Planning and preparation for production events including preparing of processing plan memos. etc. | 6/17/2020 |
| 10850 | Pace Analytical Maplewood, MN Chemist - Pharmaceutical HPLC MS in chemistry or related science Exp: 1+ year(s) |
Candidate will provide analytical chemistry support to marketed inhalation or transdermal products. This may include routine or complex analysis, method development and/or validation and technical document authoring. Candidates will utilize chromatographic techniques such as HPLC, UPLC and GC. RESPONSIBILITIES: Complete chemical or physical testing to support customer product improvements or investigations – e.g. drug content, impurities, particle size, stability, NGI, and other chromatographic and non-chromatographic characterization tests. Utilize HPLC/UPLC, GC and other chromatographic methods. Participate in method development and/or validation as needed. etc. | 6/17/2020 |
| 10851 | PAR Pharmaceutical Chestnut Ridge, NY Quality Technician II AA/AS Exp: 1-2 year(s) |
Responsible for laboratory and equipment cleanliness, routine physical and chemical testing per SOPs, and, with guidance, detects and participates in OOS/OOT and other investigations. Provides critical infrastructure support and receives, stocks and inventories reagents and supplies. Orders, receives and maintains controlled reference standards and samples. Works with metrology to perform routine daily instrument calibrations and maintenance. Communicates with the supervisor on a daily basis regarding the lab operations. Uses computer/lab software to enter the data. Understands and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. etc. | 6/17/2020 |
| 10852 | Penumbra Roseville, CA Quality Control Inspector (2nd Shift) HS diploma or equivalent Exp: 1 year |
As a Quality Control Inspector, you will test and inspect components and products in the laboratory. By ensuring that Penumbra's products meet the highest standards of quality and safety, you will play a key role in saving lives every day. This position will be working the second shift Monday through Friday from 3pm to 11:30pm. What You'll Work On: Perform routine inspection at incoming Quality Control and finished device level. Inspect components, products, labels, boxes, pouches, and coatings visually and mechanically. Take measurements using micrometers, calipers, snap gages, gage pins and other measuring instruments. etc. | 6/17/2020 |
| 10853 | Perrigo Minneapolis, MN QC Chemist II - 1st Shift BS/BA Exp: 1-2 year(s) |
Ensures the Quality and Compliance of raw materials and products by performing analytical testing on samples relative to the release of Perrigo materials and product, according to cGMP requirements. etc. | 6/17/2020 |
| 10854 | Perrigo Minneapolis, MN Quality Assurance Engineer BS in a scientific discipline Exp: 1-2 year(s) |
The QA Engineer provides primary Quality Assurance review and approval for documents such as Product Development, Process Validation, Equipment Qualification, Computer Software Validation, Method Validation, deviations, and other cGMP documentation and studies conducted at Perrigo Minnesota. KEY RESPONSIBILITIES: Supports the performance of quality risk assessments. Ensures that all information and documentation conform to company policy, cGMP’s and all other applicable FDA guidance’s. etc. | 6/17/2020 |
| 10855 | Personalis Menlo Park, CA Clinical Lab Assistant BS in molecular biology or related Exp: 0-2 years |
We are looking for a team-oriented Laboratory Assistant to join our operations team. The ideal individual must have the ability to think on their feet and troubleshoot issues. Within a dynamic startup environment, the successful candidate, under direction of the Laboratory management, will help grow the sequencing services laboratory. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. etc. | 6/17/2020 |
| 10856 | Personalis Menlo Park, CA Clinical Lab Associate BA/BS in a biological discipline Exp: 0-2+ years |
Located in Menlo Park, CA, we are seeking a talented and highly motivated Research Associate to join our Operations Team. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. This is a 3 months temp to hire position. We have Multiple openings for swing and day shifts that include one weekend day (Tues - Sat or Sun - Thurs) etc. | 6/17/2020 |
| 10857 | Phibro Sarasota, FL Fermentation Technician HS diploma or equivalent Exp: 1-3 year(s) |
Osprey Biotechnics A Division of Phibro Animal Health Corporation, is a global leader in the development of biologics, for a wide range of applications, from removing waste in ecological and industrial environments to animal health and agriculture. Osprey is currently seeking an individual, with or without experience in fermentation, for a full-time entry-level position. Specific responsibilities include but are not limited to: Operation, sanitation, assembly and disassembly of production scale fermentation and separation process equipment, along with the accompanying data entry. Receive, log, and process Diagnostic Kits. Accurately and precisely prepare and analyze samples. Equipment cleaning, assembly and sterilization of laboratory equipment. Equipment maintenance and troubleshooting. etc. | 6/17/2020 |
| 10858 | Phibro Sarasota, FL Blending Technician HS diploma or equivalent Exp: 1-3 year(s) |
The Blending Technician is an integral part of our Manufacturing team based out of our US - Sarasota, FL site. Position Details: Osprey Biotechnics is a worldwide leader in the development of bioproducts for a large range of bioremediation and bioaugmentation applications including wastewater, soil/ground water, industrial and consumer products, poultry, and agriculture. We are seeking enthusiastic, team-oriented individuals to join our blending department in this full-time, entry-level position. Specific responsibilities include but are not limited to: Prepare media; Set up, operate, clean and maintain equipment at the bench. Able to perform repetitive bench and line bottling operations. Follow, and maintain Standard Operation Procedures. Have strong attention to detail. etc. | 6/17/2020 |
| 10859 | PPD Boston, MA Scientist / Senior Scientist- HPLC , GC , KF , Analytical Development MS in chemistry, engineering, or related Exp: 1+ year(s) |
As an Scientist / Sr. Scientist, you will use state-of-the-art technologies to perform traditional and innovative analytical techniques and Quality-by-Design principles to develop and validate the analytical tools used to ensure the safety, efficacy and quality of the customer pharmaceutical products. As a member of the Analytical Development team, you will provide project support to the drug development programs at the customer site through laboratory techniques commonly used in the analysis of pharmaceuticals such as HPLC, GC, and KF. etc. | 6/17/2020 |
| 10860 | PPD Richmond, VA QA Auditor I - Labs - Vaccines BS in biology or forensic science Exp: 1-2 year(s) |
Summarized Purpose: Assures the quality of lab data and reports. Conducts internal and/or external audits to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and/or client contractual obligations. Identifies and addresses non-conformance issues. Assists in the delivery of quality services for contracted quality assurance audits, internal site audits, laboratory audits and file audits for clients and projects. Applies company policies and procedures to resolve routine issues. etc. | 6/17/2020 |
| 10861 | Paradigm (Exact Sciences) Madison, WI Materials Management Associate I - Monday - Friday, 4:00pm - 12:30am shift AA/AS in business, operations, or related Exp: 1+ year(s) |
The Materials Management Associate I will assist in a variety of Materials Management functions including but not limited to purchasing, inventory management, packaging, shipping, receiving and distribution of goods and supplies. This position will work within defined protocols and procedures. This is a second shift position with the days and hours of Monday - Friday, 4:00pm - 12:30am shift. Essential Duties and Responsibilities include but are not limited to the following: May receive, verify, inventory or deliver incoming materials. May facilitate shipment of outgoing materials or products. etc. | 6/17/2020 |
| 10862 | Paragon Genomics Hayward, CA Manufacturing Technician BS in a biological science or related Exp: 1 year |
Paragon Genomics is a fast-growing life sciences company developing advanced reagents and assay kits for next-generation sequencing (NGS). We’re seeking a temporary Manufacturing Associate with a molecular biology background and basic technical knowledge of manufacturing operations. The ideal candidate has knowledge of and experience with current Good Manufacturing Practice (cGMP) and Standard Operating Procedures (SOPs). The ideal candidate will have wet-lab technical skills in NGS library preparation, target enrichment or molecular biology, in general. There is an opportunity for permanent placement for the candidate who demonstrates competence and a willingness to learn new responsibilities. etc. | 6/17/2020 |
| 10863 | PAR Pharmaceutical Chestnut Ridge, NY Packaging Operator l - 2nd Shift HS diploma or equivalent Exp: 0 years |
Learns and performs basic functions relating to the packaging of drug products consistent with established Current Good Manufacturing Practices (cGMP), customer requirements and in conjunction with all Standard Operating Procedures (SOP). Responsible for the safe and efficient execution of job duties, while ensuring product compliance to established standards. Responsibilities: Packaging Operations: Learns and executes under supervision the skills necessary to operate pharmaceutical packaging machinery which may include stamp machines, tape machines, box machines, electronic scales, and other machinery. Learns and executes processes such as: material handling, capping, outserts/med guides, in-process checks, packing, stacking, cartoning, etc. May learn and perform basic equipment set ups. etc. | 6/17/2020 |
| 10864 | Perrigo Covington, OH QC Chemist II - 1st Shift, 2/2/3 Schedule BS in chemistry, food science, or biology Exp: 1-2 year(s) |
We are currently looking for a highly motivated QC Chemist who will work 1st shift on a rotating 2/2/3 schedule. Description: Collect samples including raw material, finished product, process equipment and environmental. Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations. Operate laboratory equipment. Participate in internal and external quality audits. Maintain personal laboratory work area and assist with general laboratory cleaning. etc. | 6/17/2020 |
| 10865 | Penumbra Roseville, CA Manufacturing Engineer 1 (Equipment) BS in mechanical, biomedical, chemical, or materials engineering Exp: 0-2 years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. We are looking for an engineer to play a key role in manufacturing processes, interact between production and cross-departmental engineering groups in resolving problems encountered with equipment, and serve as the subject matter expert for manufacturing equipment. What You'll Work On: Optimize production processes by designing fixtures, acquiring off-the-shelf tooling and equipment, and implementing new fixturing on the production line. Perform equipment qualifications. etc. | 6/17/2020 |
| 10866 | Noxilizer Hanover, MD Laboratory Technician I BS in biology, chemistry, or related Exp: Recent graduates |
Noxilizer, a pioneer in the development of a new sterilization technology, is seeking a Laboratory Technician I. Work in a creative team environment for a small, fast-paced, growing medical device manufacturer. Join a high-performing team of microbiology and material compatibility leaders to solve sterilization challenges. MAJOR DUTIES AND RESPONSIBILITIES: Perform basic laboratory tasks such as: Prepare, test, and analyze material for laboratory product development, prepare sterile solutions, etc. | 6/16/2020 |
| 10867 | Nuvasive Memphis, TN Picker/Packer, 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties: Compares nomenclature, stock numbers, and other listed information on packing slips to verify accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. etc. | 6/16/2020 |
| 10868 | Nuvasive Aliso Viejo, CA Manufacturing Technician HS diploma or equivalent Exp: 1+ year(s) |
Job Description: Align, fit, and assemble component parts, using hand tools, power tools, fixtures, and templates. Analyze and record test results per acceptance test criteria, and prepare written testing documentation. Organize work areas. Install electrical and electronic parts and hardware in housings or assemblies, using soldering equipment and hand tools. Read blueprints, schematics, diagrams, manufacturing instructions, and work orders to determine methods and sequences of assembly. Repair, rework, and calibrate assemblies and systems to meet operational specifications and tolerances. etc. | 6/16/2020 |
| 10869 | Ology Bioservices Alachua, FL Biomanufacturing Associate I-III, Downstream Night Shift BS in biology, microbiology, chemistry, or similar field Exp: Not necessary for BS candidates |
This position will assist in production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). Essential Position Responsibilities: Assist with upstream related activities including cell culture at small and large scale, cell transfection, media and buffer preparation, and bioreactor and fermenter-based production. Assist with downstream related activities including chromatography purification, centrifugation and ultracentrifugation, ultrafiltration/ diafiltration, and viral clearance. etc. | 6/16/2020 |
| 10870 | Ology Bioservices Alachua, FL Biomanufacturing Associate I - II AS/BS in biology, microbiology, chemistry, or related Exp: 0-1 year(s) |
This position will assist in production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). Assist with upstream related activities including cell culture at small and large scale, cell transfection, media and buffer preparation, and bioreactor and fermenter-based production. Assist with downstream related activities including chromatography purification, centrifugation and ultracentrifugation, ultrafiltration/ diafiltration, and viral clearance. Assist in drafting Standard Operation Procedures, Change Controls, and Deviations. Properly disinfect. etc. | 6/16/2020 |
| 10871 | Olympus Southborough, MA Market Quality Engineer I BS in an engineering discipline, microbiology, chemistry, or quality assurance Exp: 1-2 year(s) |
The Quality Market Engineer I maintains responsibility for performing product surveillance activities for all medical devices and is responsible for assisting in the investigation of complaints and reportable events. He/ she interfaces with OEMs and local departments to promote quality improvements to both products and quality system processes by initiating and driving corrective and preventive actions. The incumbent identifies and proposes solutions to quality discrepancies and process improvements based on data collection, trend analysis and reporting activities. He/ she must be able to communicate and follow-up on event description detail with internal and external customers in order to evaluate adverse event occurrences. They provide supports in the continuous improvement effort of the MSG quality system for processing complaints in order to meet FDA, ISO and all applicable international regulatory requirements, and corporate guidelines. etc. | 6/16/2020 |
| 10872 | Olympus Bartlett, TN Global MDR Submission Analyst II BS Exp: 1-3 year(s) |
As a Global MDR Submission Analyst II OSTA team member, you will be responsible for timely regulatory reporting assessments and reassessments of global complaints, preparation and submission of initial/importer/supplemental MDR reports for post market activities per 21CFR803. Performs follow-up to obtain additional information for Adverse Events by collaborating with Field Specialists, Sales Representatives, Engineers, Technicians, Clinicians, and Customers directly. Performs routine assignments with minimal direction from manager; requires general instruction for new or special assignments from Manager. The Analyst II will maintain quality documents to ensure compliance with global medical device guidance documents. The Analyst II requires working knowledge of Medical Device Quality Systems regulations including ISO 13485, 21CFR820, and 21CFR803. etc. | 6/16/2020 |
| 10873 | Olympus State College, PA Assembler II HS diploma or equivalent Exp: 1-2 year(s) |
The Assembler II supports Manufacturing Operations by assembling high-quality small format medical devices in accordance with established procedures and in support of the production schedule. An Assembler II is also expected to assist with training less experienced assemblers. Job Duties: In a typical day, you will: Interacts primarily with varying levels of Manufacturing Engineering and Research team members. May interact with external customer contacts including participating in tours by visitors including VIPs and may be questioned and/or observed during audits. Assembles components into medical devices in accordance with approved manufacturing procedures. Assembly may be in clean rooms and may involve assembly of miniature components under a microscope. etc. | 6/16/2020 |
| 10874 | Opgen Gaithersburg, MD Lab Tech I BS in molecular biology, microbiology, biochemistry, biology or related Exp: 6+ month(s) |
The Laboratory Technician I will perform a variety of procedures to support the workflow of the Production Operations. The Laboratory Technician I will be responsible for performing support functions for various routine and non-routine manufacturing operations such as reagent formulation, product testing and validation, equipment calibration, etc. The Laboratory Technician I is expected to follow validated procedures with occasional direct supervision from the Manufacturing Supervisor. Essential Duties and Responsibilities: Formulate, fill and package consumables according to Company SOPs and cGMP guidelines. Monitor and maintain laboratory supplies and laboratory equipment. etc. | 6/16/2020 |
| 10875 | Ora Andover, MA Clinical Trial Associate BS/BA Exp: 1+ year(s) |
At Ora, our Clinical Trial Associates assists project managers in clinical study conduct for clinical projects, supports the oversight of all investigator sites and ensures compliance with protocol/overall clinical objectives. Performs day to day activities under the guidance of the Sr. CTA/Lead, Assistant Project Managers and Project Managers. PRIMARY RESPONSIBILITIES: Ensure trials are conducted in adherence to study protocols, applicable SOPs, EMA, FDA regulations, ICH/GCP guidelines and government regulations. Drafts and/or reviews study-related documents and templates including study protocols, informed consents, source document templates, study plans, study related logs, etc. | 6/16/2020 |
| 10876 | OraSure Technologies Bethlehem, PA Quality Control Specialist I AS/BS in chemistry, biology, medical technology, or related science Exp: 1 year |
Quality Control Specialist I personnel perform procedures that include evaluation of raw materials, in-process components, finished products, stability testing, equipment quality control, and equipment maintenance in compliance with guidelines established by Orasure Technologies and regulatory agencies. Responsibilities: Perform all procedures accurately and according to written Work Instructions and SOPS as indicated in the Quality Control procedures and other applicable facility procedures. Perform testing at all levels of production including raw materials, in-process components, finished products and stability testing. Perform visual finished product inspections. etc. | 6/16/2020 |
| 10877 | OraSure Technologies Bethlehem, PA Manufacturing Engineer BS in chemical, mechanical, or manufacturing engineering Exp: 1-2 year(s) |
Support and optimize the manufacturing and packaging of disposable diagnostic devices. Support projects which may include new products, new equipment, process improvements, and cost reductions. ESSENTIAL DUTIES AND RESPONSIBILITIES: Support production operations by trouble shooting and repairing automated assembly and packaging equipment in conjunction with the Maintenance team. Investigate manufacturing yield or product nonconformance issues, determine root causes, and implement corrective and preventative actions. Develop and revise manufacturing process documentation including material specifications, component and assembly drawings, and work instructions. etc. | 6/16/2020 |
| 10878 | Organogenesis Norwood, MA Materials Handler HS diploma or equivalent Exp: 1 year |
Key responsibilities: Receives and labels incoming materials. Delivers materials to internal customers. Produce labels for finished products. Product labeling and packaging. Assist in the daily scheduling of activities. Prepare and package outgoing product shipments. Print and prepare documentation. Complete cycle counts and inventory checks in a timely and accurate manner | 6/16/2020 |
| 10879 | Bausch Health Greenville, SC Distribution Associate HS diploma or equivalent Exp: 1 year |
Receiving operation is responsible for accurately receiving product from the B&L Manufacturing Operation along with other third-party vendors, putting product into assigned storage locations, and retrieving product and delivering it to the pick area and/or shipping lanes. Also, perform shipping duties including preparing orders for shipment consisting of pallet stacking, labeling and wrapping. All order transaction controlled via RF computer. Shipping operation is responsible for accurately retrieving product from the pick area. Also, perform shipping duties including pallet stacking, labeling and wrapping. Other responsibilities include truck loading and general warehouse housekeeping. All order transaction controlled via RF computer. etc. | 6/16/2020 |
| 10880 | Bausch Health Tampa, FL Microbiology Technician III - 2nd Shift BS in microbiology, biology, or related Exp: 1-2 year(s) |
Objectives: Perform routine testing for release of raw materials, finished products, stability samples and R&D products. Perform Environmental and Utility Monitoring in aseptic areas. Responsibilities: Perform routine assays for endotoxin, potency, sterility, bioburden, microbial limits, and preservative effectiveness on various finished products and/or raw materials. Perform identification of organisms. Maintain laboratory culture collection and preserve cultures. Contribute to the preparation and checking of environmental summaries. Perform testing in conjunction with laboratory investigations. Perform Environmental and Utility monitoring. Perform testing in support of facility Validation activities. etc. | 6/16/2020 |
| 10881 | Bausch Health Rochester, NY Microbiology Technician IV HS diploma/BS in a life science Exp: 1-2 year(s) |
Conduct environmental monitoring (EM) per specifications for the Rochester Manufacturing Plant. Support the EM program through analysis and communication by adhering to established guidelines. Contributes as a team member and performs specifically defined work/projects. May participate in quality projects or teams. Responsibilities: Support environmental/water monitoring for the Rochester Plant. Specific responsibilities include scheduling, sampling, testing, and maintenance of supplies. Perform microbiological testing as part of the core competency function. Includes routine testing and validation support to the Rochester Plant and R&D. Initiation of NCR when pre-established levels are exceeded. may assist with root cause investigations/CAPAs when necessary. Preparation/review of memos, reports, SOPs, and protocols. etc. | 6/16/2020 |
| 10882 | OraSure Technologies Ottawa, ON Lab Technologist, Validation & Compliance BS/MS in biochemistry or molecular biology Exp: 1+ year(s) |
As part of Research & Development, the Lab Technologist position is responsible for testing as it relates to the DNA Genotek portfolio of products. In this role, the Lab Technologist will be responsible for managing testing timelines, performing hands-on lab work (e.g. extraction and quantification of DNA from biological samples, kinetic enzyme assays), summarizing data, and communicating the results with the team. Responsibilities: Performs experiments to assist in solving scientific problems of interest to the company, with guidance from a Research Associate or Scientist. Executes, and analyzes experiments. Performs hands-on laboratory experimental work. Communicates ideas and participates in scientific discussions. etc. | 6/16/2020 |
| 10883 | OraSure Technologies Bethlehem, PA Formulation Specialist BS in chemistry, biochemistry, or equivalent Exp: 1-3 year(s) |
Manufacture the chemical formulations necessary for production of all products. Responsibilities: Coordinate and prepare all chemical formulations according to batch production records (BPR). Responsible for changing documents when necessary (CTN). Assist in writing and performing validation protocols, nonconformance investigations and planned deviation investigations. Evaluate reagents, raw materials and in-process components through visual and performance testing according to specifications. Recommend acceptance or rejection of raw materials, and in-process components based upon established specification and procedures. Be responsible for the accuracy and completeness of material inventory records. Inform supervisor or approved designee to order inventory and supply items as needed. etc. | 6/16/2020 |
| 10884 | Nuvasive Memphis, TN Associate Sterile Processing Technician HS diploma or equivalent Exp: 1+ year(s) |
Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties. Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in-process production reports, and status of material locations. etc. | 6/16/2020 |
| 10885 | Nuvasive San Diego, CA Development Engineer BS in mechanical or biomedical engineering or related Exp: 0-2 years |
NuVasive is seeking a Mechanical or Biomedical Engineer for our Mechanical Systems Integration team. As a Development Engineer within our team, you’ll be responsible for the design and development of medical devices with enhanced features that allow integration with our navigation and robotics enabling technology platform to treat spinal pathologies in accordance with US and international regulations. You will gain hands-on experience developing innovative mechanical solutions to meet patient and surgeon needs from concept to commercialization. This requires working in cross-functional teams, including marketing, purchasing, regulatory, quality, research and testing, manufacturing, etc., to help manage the product development process, project timeline, and deliverables to ensure designs are safe and effective for clinical use. etc. | 6/16/2020 |
| 10886 | Nuvasive West Carrollton, OH Material Handler -1st shift HS diploma or equivalent Exp: 1+ year(s) |
The Associate Distribution Coordinator Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties. Compares nomenclature, stock numbers, and other listed information on packing slips to verify accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in process production reports, and status of material locations. Compiles information on receipt of disbursement of material, equipment, merchandise, or supplies, and computes inventory balance, price, and cost. etc. | 6/16/2020 |
| 10887 | Miltenyl Biotec Auburn, CA Logistics Associate HS diploma Exp: 1 year |
As a member of the Miltenyi Biotec team, you will help ensure that the shipping and receiving process runs efficiently for our growing biotechnology organization. You will prepare and process inventory using your Enterprise Resource Planning (ERP) and shipping systems knowledge. In addition, you will record and receive incoming shipments according to established SOPs, as well as prepare and process shipments according to international regulations. There will also be occasion for employing hand-trucks and forklifts in order to move and store certain articles during routine inventory maintenance. etc. | 6/16/2020 |
| 10888 | Miltenyl Biotec Cambridge, MA Clinical Trial Associate BS/BA Exp: 0-2 years |
Your Tasks: Collaborate with Clinical Trial Managers to assist in the operational and logistical aspects of clinical trial management tasks. Act as a liaison with CROs and other clinical vendors to ensure deliverables are met. Partner with Investigators and clinical site staff to ensure optimal Sponsor-Site relationships. Proactively Assist in the management of studies to ensure adherence to timelines and identify investigative site risks, proposing corrective actions. Serve as Functional TMF Document Specialist for Clinical Operations, to include submission of documents to and maintenance of the TMF. etc. | 6/16/2020 |
| 10889 | CSL Halethorope, MD Quality Specialist Associates or BS/BA in business admine or biological sciences Exp: 1 year experience |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 6/14/2020 |
| 10890 | CSL Holly Springss, NC Associate I/II/III, Manufacturing (Fill Finish Expansion) Aseptic - Day Shift BS/BA in sciences or engineering preferred Exp: 1 year in pharma/biotech |
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (be trained in) the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant, efficient, and cost effective manner. Becomes trained on basic processes and equipment and serves as a hands-on resource in Production. Cleaning, preparing, and sterilizing production equipment | 6/14/2020 |
| 10891 | CSL Cheektowaga, NY Medical Screener - Reception Technician HS Diploma/GED Exp: 3 months in clerical/customer service |
n compliance with Standard Operating Procedures (SOPs), assists qualified donors in completing the screening process. The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the donation process, referring donors to medical staff when appropriate and performing health screening procedures such as blood pressure, pulse, weight, temperature. Performs finger stick to obtain sample to obtain donor’s hematocrit and total protein levels. | 6/14/2020 |
| 10892 | CSL Springfield, OH Plasma Processing Technician HS Diploma/GED Exp: 3 months in lab/warehouse |
In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. Ensures accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. | 6/14/2020 |
| 10893 | CSL Indianapolis, IN Customer Service - Donor Support Technician HS Diploma/GED Exp: 3 months in med/health environment |
Prepares the autopheresis machine for the pheresis process. Monitors the donor and the pheresis process, responds to specific alarms or signals that may occur during the process. Disconnects the donor when the process is complete. Maintains alertness and awareness to any reaction donor may have during or after the pheresis process and notifies appropriate staff. Uses Personal Digital Assistant (PDA) to record incidents that occur during the pheresis process, such as machine alerts and alarms, volume variances and donor adverse events. | 6/14/2020 |
| 10894 | CSL Hillsboro, OR Phlebotomist HS Diploma/GED Exp: 1 year in med/health environment |
In compliance with SOPs, performs all aspects of the pheresis procedure and plasma collection, including donor set-up, donor monitoring and donor disconnect. In compliance with SOPs and Food & Drug Administration (FDA) guidelines, performs venipuncture on donors to begin pheresis process. Evaluates vein performance of the donor to identify possible problems; makes necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments when necessary to make the process a positive experience for the donor. | 6/14/2020 |
| 10895 | CSL Temple Terrace, FL Phlebotomist HS Diploma/GED Exp: 1 year in med/health environment |
In compliance with SOPs, performs all aspects of the pheresis procedure and plasma collection, including donor set-up, donor monitoring and donor disconnect. In compliance with SOPs and Food & Drug Administration (FDA) guidelines, performs venipuncture on donors to begin pheresis process. Evaluates vein performance of the donor to identify possible problems; makes necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments when necessary to make the process a positive experience for the donor. | 6/14/2020 |
| 10896 | CSL Tuscson, AZ Customer Service - Donor Support Technician HS Diploma/GED Exp: 3 months in med/health environment |
Prepares the autopheresis machine for the pheresis process. Monitors the donor and the pheresis process, responds to specific alarms or signals that may occur during the process. Disconnects the donor when the process is complete. Maintains alertness and awareness to any reaction donor may have during or after the pheresis process and notifies appropriate staff. | 6/14/2020 |
| 10897 | CTI Covington, KY Clinical Safety Scientist I BS or RN Exp: 1-2 years work experience, GCP Training |
The Clinical Safety Scientist I is responsible for managing serious adverse events (SAEs) in clinical trials or post-marketing programs, focusing on all aspects of the collection, processing, evaluating and reporting of cases in accordance with CTI’s Global Drug Safety and Pharmacovigilance processes, International Council for Harmonisation (ICH) guidelines, Good Clinical Practices (GCP), applicable regulatory guidelines and study procedures. This individual will track cases from receipt to closure, perform verification of safety data, and will utilize clinical / pharmacovigilance judgment in coding of serious events and synthesizing complex clinical information into accurate and complete narratives. | 6/14/2020 |
| 10898 | CTI Raleigh, NC Clinical Safety Scientist I BS or RN Exp: 1-2 years work experience, GCP Training |
The Clinical Safety Scientist I is responsible for managing serious adverse events (SAEs) in clinical trials or post-marketing programs, focusing on all aspects of the collection, processing, evaluating and reporting of cases in accordance with CTI’s Global Drug Safety and Pharmacovigilance processes, International Council for Harmonisation (ICH) guidelines, Good Clinical Practices (GCP), applicable regulatory guidelines and study procedures. This individual will track cases from receipt to closure, perform verification of safety data, and will utilize clinical / pharmacovigilance judgment in coding of serious events and synthesizing complex clinical information into accurate and complete narratives. | 6/14/2020 |
| 10899 | Morphic Therapaeutics Waltham, MA Research Associate II, Translational Sciences MS in relevant Exp: 1-2 years in pharmacology/physiology, etc. |
Help transform common analytical methods into clinically meaningful endpoints for patients. Develop and trouble shoot new and innovative assays. Perform ex vivo sample analysis on a wide array of technology platforms in support of lead project development. Gain familiarity with state of the art technologies and help determine best path to success for a given project. | 6/14/2020 |
| 10900 | Sage Therapuetics Cambridge, MA Coordinator, Research Operations BS/BA Exp: 0-3 years |
Responsible for managing the Research Publication process, including but not limited to publication roadmap planning, approval processing, adherence to policies/procedures, stakeholder management, and research publication team logistics. Responsible for research vendor management, including but not limited to representation and evaluation of the research vendor management landscape, performance and business oversight of active vendors, and evaluation of potential new vendors. | 6/14/2020 |
| 10901 | Cyanotech Kailua-Kona, HI Extraction Operator HS Diploma/GED Exp: 1 year work in production |
This is a Temporary position through Altres. Responsible for operating supercritical CO2 extraction equipment used to remove high-value lipids from Haematococcus. Ensures safe and sustainable production of extraction products. Safely completes plant cleaning, basket loading and unloading, packing, and other tasks as required to prevent operating delays. | 6/14/2020 |
| 10902 | Cyanotech Kailua-Kona, HI Harvest Processor (swing & grave shift) HS Diploma/GED Exp: 1 year work in production |
This is a full-time, non-exempt position. Responsible for processing Spirulina and Astaxanthin. Includes operating all processing equipment and packaging the finished product. Also responsible for shutdown, sanitation and startup of processing systems. Employees in this position will work a designated shift (day shift, swing shift, or graveyard). | 6/14/2020 |
| 10903 | CryoLife Kennesaw, GA Microbiology Technician II BS in microbiology or related Exp: 1-2 years in lab |
Perform microbiological testing for human tissue and medical device samples, as well as perform environmental and water monitoring. Monitor cultures for the presence of microbial growth. Hours: Mon, Tues, Wed, Fri from 7am-5:30pm | 6/14/2020 |
| 10904 | CryoLife Kennesaw, GA DQA Analyst BS/BA in biological sciences Exp: 1-2 years in |
To coordinate the activities necessary to ensure that all donor records flow through the system with minimal delay. Provide a leadership role for entry level DQA individuals. Ensure that all areas outlined under “Principal Responsibilities” are accomplished in an efficient, professional manner. Read, critique, review and complete DQA form reviews per QA0175, QA0176 and QA0079 as delegated by DQA Management. | 6/14/2020 |
| 10905 | CryoLife Kennesaw, GA Microbiology Associate BS/BA in life sciences preferred, HS Diploma minimum Exp: 1-3 years in lab |
Will assist management in the review of Microbiology records to ensure they are compliant with required Standard Operating Procedures. Will ensure that all areas outlined under “Principal Responsibilities” are accomplished in an efficient, professional manner. Interface with Microbiology staff and other applicable personnel to clarify and/or correct the information provided, and to solicit required information. Understand ISO requirements, GTPs and the Quality System Regulations as they pertain to the Laboratory, i.e., nonconformities, Good Documentation Practices, calibration, equipment maintenance, etc. | 6/14/2020 |
| 10906 | CryoLife Kennesaw, GA Process Engineer I BS in engineering or life sciences Exp: 0-2 years |
Responsible for providing process engineering support for all product manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as develop new processes to improve manufacturing efficiency. | 6/14/2020 |
| 10907 | Cue Cambridge, MA Contract Associate Scientist – Translational Immunology MS in relevant Exp: 0-2 years |
We are looking for a motivated Contract Associate Scientist to join our Translational Immunology/Immuno-Oncology group to provide key mechanistic, pre-clinical and translational support for Cue Biopharma’s growing pipeline. The Contract Associate Scientist will be part of the company’s TCR Core, a team dedicated to generating and performing key studies with T Cell Receptors – TCR-transduced human cell lines and primary human T cells. This is a temporary contract position that could last up to six (6) months. | 6/14/2020 |
| 10908 | Cyanotech Kailua-Kona, HI Cultivation Lab Technician BS in aquaculture, biology, life sciences Exp: 1 year in lab and/or algal production or aquaculture |
This position is responsible for Spirulina production system data and adjustments as necessary to stay within set operating specifications. This position will be responsible for the data necessary to track Spirulina system performance as well as data necessary for operational set point adjustments necessary to stay within system specifications, such as nutrient analyses, pond data, and harvest/processing data. | 6/14/2020 |
| 10909 | Core Rx Clearwater , FL Facilities Technician I HS Diploma/GED Exp: 1+ years in building maintenance |
Facilities Technicians are responsible for a variety of semi-skilled and skilled day-to-day facility operations, the scheduled, unscheduled and preventative maintenance and repair of a wide variety of facility systems and manufacturing equipment, and require a strong mechanical skill base to include but not limited to HVAC, compressed air components and systems, generators, building management systems, control logic systems, security systems, water conditioning systems, electrical, lighting, fenestration, plumbing, drywall, and general landscape maintenance. | 6/13/2020 |
| 10910 | Corium Grand Rapids, MI Operator I - Weekend Days HS Diploma/GED Exp: 1-2 years in cGMP environment preferred |
Currently, we seek an Operator I to work the weekend day shift at our Grand Rapids facility. The Operator I will set up and operate extrusion equipment to produce products to meet cGMP, customer and internal quality standards for our Grand Rapids facility. As an Operator I, you will: Set-up and operate extrusion equipment. Perform basic maintenance and troubleshooting of equipment. Ensure production crew is on task and focused on safety, quality, and productivity | 6/13/2020 |
| 10911 | CovalX Saugus, MA ENTRY LEVEL FIELD/LAB ENGINEER BS in engineering or life sciences Exp: Entry Level |
The position will involve completing final assembly and testing of our high mass MALDI detector systems, followed by installation of these systems at customer sites. Due to the novelty of many of the required tasks, training will be provided by CovalX.Additionally, design projects overseeing new product development will be required. | 6/13/2020 |
| 10912 | CovalX Saugus, MA Entry level Sales Associate BS/BA in life sicneces Exp: 1+ years experience |
Conduct marketing and sales independently in large and small biotech accounts. Create and execute sales strategy with the support of your manager. Achieve defined metrics for sales activity and revenue growth. Support tradeshow marketing and booth staffing. | 6/13/2020 |
| 10913 | Covance Ann Arbor, MI Research Analyst BS/BA in life sciences Exp: 0-1 years, includes internships |
The Research Assistant I is responsible for the performance of pharmacological tasks associated with both client and internal studies which are under the direction of the assigned study manager (typically a Group Leader, Associate Scientist or Senior Associate Scientist). Handle, manipulate and restrain small animals to conduct procedures, including but not limited to, health checks, weighing, measuring and dosing by multiple routes: PO, IP, IV, SC, IM, ID, IT, blood collection, tissue excision, and implants. Accurately report clinical signs under guidance from supervisor. | 6/13/2020 |
| 10914 | Crinetics San Diego, CA RESEARCH ASSOCIATE, DRUG METABOLISM AND PHARMACOKINETICS (DMPK) BS/BA/MS in sciences Exp: 1-2 years |
The work will support projects at various stages drug discovery and development thereby allowing the selected candidate to play an active role in our drug discovery and development efforts to advance small molecule therapeutics for rare endocrine disorders and endocrine-related cancers. Perform DMPK assays for small molecules such as in vitro metabolic stability, CYP inhibition, reaction phenotyping, and metabolite profiling/identification | 6/13/2020 |
| 10915 | CRISPR Theraputics Cambridge, MA Research Associate/Research Associate II, Immuno-Oncology BS or MS in biology Exp: 1-2 years lab biology experience |
We are looking for Research Associates (all levels) to join the Immuno-Oncology Groups at CRISPR Therapeutics in Cambridge, MA (oncology). Successful candidates will be integral to developing next generation cellular therapeutics with an emphasis on genetically engineering immune cells to increase their therapeutic potential. Molecular biology skills are required for this position and should have enthusiasm, passion, and a desire to create important new medicines for patients. | 6/13/2020 |
| 10916 | Covance Indianapolis, IN Medical Technologist I BS/BA in med technology or clinical lab sciences Exp: 1 year med tech training program |
Resolve technical specimen issues in preparation for analysis and specimen storage and routine and non-routine assay problems. Ensure the validity of test results through the performance of established quality assurance and quality control procedures. Perform experiments, as scheduled, for evaluation of new Calibrator and QC lots. Perform testing, needed to ensure validity of material, prior to being placed into service | 6/13/2020 |
| 10917 | Covance Indianapolis, IN Medical Technologist I (PRN) BS/BA in med technology or clinical lab sciences Exp: 1 year med tech training program |
Resolve technical specimen issues in preparation for analysis and specimen storage and routine and non-routine assay problems. Ensure the validity of test results through the performance of established quality assurance and quality control procedures. Perform experiments, as scheduled, for evaluation of new Calibrator and QC lots. Perform testing, needed to ensure validity of material, prior to being placed into service | 6/13/2020 |
| 10918 | Covance Madison, WI Sample Handling Assistant I HS Diploma/GED Exp: 0 years required |
Performs a variety of Sample Management and/or Archives responsibilities in compliance with appropriate SOP’s and Good Laboratory Practice (GLP), Good Clinical Practice (GCP) or Good Manufacturing Practice (GMP) regulations (as appropriate) in support of various Business Unit Operations. Ensures that services to both internal and external customers are provided in a timely manner or as agreed in Service Level Agreements. | 6/13/2020 |
| 10919 | Covance Madison, WI Nonclinical Data Associate BS/BA in computer sciences/informatics Exp: 1-3 years, entry level |
This is an entry level Nonclinical Data Associate position with a primary function of drafting and finalizing nonclinical datasets. Performing quality control review datasets using industry data standards using (e.g. SEND, SDTM, SENDIG). May compile metadata to populate databases supporting nonclinical safety assessment. May assist with software testing and validation activities: including executing test scripts and maintaining documentation in accordance with Covance Unified Systems Life Cycle (CUSLC) methodology which complies with General Principles of Software Validation issued by the FDA. | 6/13/2020 |
| 10920 | Covance Dallas, TX Research Nurse I Associates or BS in nursing with licensure Exp: 1-2 years in research |
As a Clinical Research Nurse for Covance your top priority will be to ensure that the dignity, health, safety, and welfare of participants. This position will be office based in Dallas, TX. This will be a rotating shift to either work Day, mid or overnight shifts as needed. Utilize nursing assessment skills to observe participant general well-being and potential adverse events. Document adverse events and takes appropriate action as needed. | 6/13/2020 |
| 10921 | Covance Indianapolis, IN Histology Technician HT(ASCP) certification as histoltechnologist Exp: 1 year in research/histology |
Process daily samples according to written procedures prior to end of day utilizing histology techniques of cryotomy, microtomy, tissue grossing, tissue embedding, routine staining, special staining, immunohistochemistry (IHC) and fluorescence in-situ hybridization (FISH). Maintain accurate documentation and paper work to provide a sample audit trail. Communicate sample enquiries and issues via email to internal and external clients and work well as a part of a team as well as independently | 6/13/2020 |
| 10922 | Cardinal Health Chicopee, MA Assembler II - Hydra - 2nd Shift HS Diploma/GED Exp: 1-3 yearas |
Performs a variety of tasks ranging from repetitive to non-repetitive production to put together component parts to make assemblies, sub-assemblies or completed units, using standard operating procedures. May conduct quality inspections on processing line in accordance with quality specifications. | 6/13/2020 |
| 10923 | Cardinal Health Obetz, OH Associate II, Warehouse Operations (Second Shift) HS Diploma/GED Exp: 1-2 years related |
Warehouse Operations is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. Also responsible for the efficient flow of products from the point of product receipt from vendors to the shipment of products (via prescribed service parameters) to a variety of internal and external customers | 6/13/2020 |
| 10924 | Cardinal Health La Vergne, TN Associate II, Warehouse Operations HS Diploma/GED Exp: 1-2 years related |
Warehouse Operations is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. Also responsible for the efficient flow of products from the point of product receipt from vendors to the shipment of products (via prescribed service parameters) to a variety of internal and external customers. | 6/13/2020 |
| 10925 | Cardinal Health Omaha, NE Inventory Associate HS Diploma/GED Exp: 1-2 years related |
Inventory Management is accountable for the design and execution of demand planning and customer forecasting systems, supply planning, product deployment and expediting processes, and the development and implementation of a stocking optimization model to minimize costs and inventory while delivering on service requirements. | 6/13/2020 |
| 10926 | Cardinal Health Charlotte, NC Lab Technician - Nights BS/BA in sciences Exp: 1-2 years in lab |
The primary work environment consists of a cyclotron and associated manufacturing facility for the production of PET radiopharmaceuticals, which must be kept clean, orderly, properly lighted and maintained in optimum operating condition. Successfully complete extensive training, including e-learning assignments and hands on components, to demonstrate and maintain proficiency. Manufactures radioactive isotopes (includes synthesis set up, hot cell manipulations, distribution). | 6/13/2020 |
| 10927 | Cardinal Health Crystal Lake, IL Manufacturing Associate I - C Shift - Contract Conversion HS Diploma/GED Exp: 1-3 months training, 0-6 months work experience |
Sets up and operates a variety of machine tools to make metal parts, mechanisms, tools, or machines to exacting tolerances and dimensions. determines sequence of operations, number of cuts required, and method of setup. Interprets blueprints, sketches, and engineering specifications. makes standard shop computations relating to dimensions of work, tooling, feeds, and speeds | 6/13/2020 |
| 10928 | Cardinal Health Crystal Lake, IL Manufacturing Associate II - Syringe - B Shift - Contract Conversion HS Diploma/GED Exp: 1-3 years of work/training |
Sets up and operates a variety of machine tools to make metal parts, mechanisms, tools, or machines to exacting tolerances and dimensions. determines sequence of operations, number of cuts required, and method of setup. Interprets blueprints, sketches, and engineering specifications. makes standard shop computations relating to dimensions of work, tooling, feeds, and speeds | 6/13/2020 |
| 10929 | NAMSA Irvine, CA Microbiology Technologist BS/BA Exp: No experience required |
Principal Duties and Responsibilities: May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. etc. | 6/10/2020 |
| 10930 | NAMSA Northwood, MA Chemist MS/MA Exp: No experience required |
Job Description: Independently conduct testing according to written instructions. May be requested to conduct more involved studies. May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. May conduct routine testing per NAMSA SOPs as well feasibility, protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP, etc. Works with management to ensure large studies are completed on or before the due date. Prepare and maintain the reagents required for testing. etc. | 6/10/2020 |
| 10931 | Natera San Carlos, CA Research Technician BS/BA in a biological science or equivalent Exp: 1-2 year(s) |
The Research Technician performs routine laboratory research and development services. Works with a multidisciplinary team. Under nominal direction, performs a variety of basic and general laboratory research and sample management tasks determined by the field and scope of the research project. PRIMARY RESPONSIBILITIES: Work primarily with R&D Scientific Operations providing biosamples for use in clinical and research efforts. Maintain the sample bank inventory and fulfill routine interdepartmental sample requests. Receive, catalog, store, and monitor biosamples to ensure chain of custody and quality. Assist in sample accessioning, pulls, distribution, and issue resolutions. Update and maintain current and incoming inventory of biosamples. Identify, label, and keep accurate sample records in LIMS/database. Perform sample inventory reconciliation. etc. | 6/10/2020 |
| 10932 | Natera San Carlos, CA Equipment Associate 1, Research & Development HS diploma/BS/BA Exp: 1+ year(s) |
The Equipment Associate 1 works primarily with the laboratory operations team and outside vendors to plan and perform various equipment handling duties. PRIMARY RESPONSIBILITIES: Maintain daily temperature logs for storage units. Work with in-house personnel or outside vendors. Monitor lab equipment for proper functionality. Vendor management: Coordinate repairs, calibrations, PMs, and RMAs with outside vendors. Ensure proper management of equipment related documentation. etc. | 6/10/2020 |
| 10933 | Natera San Carlos, CA Material Handler HS diploma or equivalent Exp: 0-1 year(s) |
The Material Handler 1 assists the team with inventory control activities to ensure products are received, moved, and stored accurately. Ensures inventory is pulled and delivered to the lab in a timely manner, and items are transacted in the company’s inventory system to reflect physical movement. Ensures items are stored in proper conditions and counted periodically for accuracy. PRIMARY RESPONSIBILITIES: Works with the lab to ensure the company is pulling inventory consumables timely and in correct quantities to not interrupt workflow. Process and record corresponding transactions in Great Plains system. Works collaboratively with the team to resolve any discrepancies. etc. | 6/10/2020 |
| 10934 | Natera Austin, TX Medical Lab Scientist I, Data Reviewer BS in medical technology or a life science Exp: 1-2 year(s) |
The Medical Laboratory Scientist I, Data Reviewer is a member of the Operations Department to review and analyze clinical test results. This individual collaborates with a team of CLS and laboratory personnel to maintain accurate records of test results and patient information, and perform any troubleshooting as needed. PRIMARY RESPONSIBILITIES: Review clinical test results of molecular genetic testing received from laboratories for accuracy and translate into LIMS. Review and analyze raw data files in proper software and resolve routine issues. Verify the proper specimen analyzed for patients and reviews the test requisition forms to verify the correct tests were performed. etc. | 6/10/2020 |
| 10935 | Natera San Carlos, CA Clinical Laboratory Scientist I BS/BA in medical technology, biological sciences, or related Exp: 1-2 year(s) |
Natera is currently seeking a licensed Clinical Laboratory Scientist I to analyze clinical laboratory specimens following the standard methods and procedures. Maintain equipment and instruments in good operating condition, recognize any malfunctions and troubleshoot as needed. PRIMARY RESPONSIBILITIES: Verify the proper specimen being analyzed and perform tests that need to be completed. Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Follows GLP (good laboratory practice): maintain clean and organized work space. Completes training and other deadlines on time. etc. | 6/10/2020 |
| 10936 | Natera Austin, TX Medical Laboratory Scientist I BS/BA in medical technology, biological sciences, or related Exp: 1-2 year(s) |
Natera is currently seeking a licensed Medical Laboratory Scientist to analyze specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: Verify the proper specimen being analyzed and perform tests that need to be completed. Proficient at analyzing clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Provides general oversight of personnel and the daily operations in the lab. Meet expected performance metrics within role as applicable. etc. | 6/10/2020 |
| 10937 | Natera Austin, TX Clinical Data (Data Entry) Operator I Swing Shift, Tuesday-Saturday HS diploma or equivalent Exp: 0-1 year(s) |
Natera is currently seeking a Clinical Data (Data Entry) Operator for swing shift to join the operations team. This position accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. PRIMARY RESPONSIBILITIES: Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning. Accession samples with high accuracy and efficiency. Accurately enter patient data into the Laboratory Inventory Management System (LIMS). Ensure that the information in LIMS is up-to-date. Scan test requisition forms and attached paperwork. Ensure that all paperwork belong to patient and upload to case. etc. | 6/10/2020 |
| 10938 | Natus Medical Middleton, WI Repair Technician (I or II) AA/AS Exp: 0-6 months |
WHAT YOU'LL GET TO DO IN THIS JOB: Test, calibrate and troubleshoot assemblies of our medical devices as well as perform electronic calibration and verify fixtures. Committing to high quality work (less than 2% failure rate on repairs) means delivering an exceptional product to healthcare providers so they can help their patients. Maintain a 10 business day repair turnaround time because getting our customers up and running means we can help more patients faster. Solve challenging problems by developing and/or designing test processes/procedures based on product specifications. Have the opportunity to cross-train to work in other areas to support business needs. etc. | 6/10/2020 |
| 10939 | Nelson Labs Salt Lake City, UT Development Chemist BS in chemistry or related Exp: 1-3 year(s) |
Looking for a Development Chemist position with a wide range of experience to work in a fast paced environment. This position involves decision making in the areas of analytical chemistry, equipment maintenance, data quality, and workflow. Duties include analysis of a wide variety of samples following establish methods or standards, and supporting the development and implementation of laboratory policies and procedures. Experience with instrumentation/equipment and software, such as gas chromatography/mass spectroscopy (GC/MS), high performance liquid chromatography/mass spectroscopy (HPLC/MS), and Inductively coupled plasma/mass spectrometry (ICP/MS). etc. | 6/10/2020 |
| 10940 | Nemera Buffalo Grove, IL Quality Engineer Quality – Buffalo Grove Unspecified Exp: 1-3+ year(s) |
Nemera needs a QUALITY ENGINEER to join our team in Buffalo Grove, Illinois. The Quality Engineer is responsible for planning, coordinating and managing through completion, assigned projects to ensure the development and production of products meets customer and internal quality deliverables. Responsibilities will also include coordinating and leading investigations regarding customer complaints, and customer interaction. etc. | 6/10/2020 |
| 10941 | Teleflex Pleasanton, CA Clinical Trial Assistant BS/BA Exp: 1-2 year(s) |
The Clinical Trial Assistant provides administrative support and assists team members in completing projects. As a key contributor to the Clinical Affairs team, this position maintains internal clinical files, supports team across multiple projects, assists with team meetings, and performs other related Clinical administrative tasks. This position requires basic knowledge of clinical regulatory requirements and clinical trials excellent organizational skills, and the ability to perform at high levels in a fast-paced, dynamic environment. Principal Responsibilities: Assist monitors and study leads on projects from study start-up to close-out. Clinical tracking and document maintenance of clinical trial sites and internal master files. Assist with the planning and management of Clinical meetings. etc. | 6/10/2020 |
| 10942 | Nephron West Columbia, SC Outsourcing Clean Room Quality Assurance On Line (Nights) HS diploma or equivalent Exp: 1-2 year(s) |
Position Summary: Monitors filling operations in compliance with company policies / procedures, FDA and cGMP regulations. Ensures the accuracy and completeness of batch records. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. The primary accountabilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Primary Accountabilities: Monitors aseptic techniques of personnel within the clean rooms. Monitors Outsourcing filling operations within the clean rooms. Verifies syringe filling rejects of Outsourcing products, as needed. etc. | 6/10/2020 |
| 10943 | Nephron West Columbia, SC Outsourcing Clean Room Quality Assurance On Line (Days) HS diploma or equivalent Exp: 1-2 year(s) |
Position Summary: Monitors filling operations in compliance with company policies / procedures, FDA and cGMP regulations. Ensures the accuracy and completeness of batch records. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. The primary accountabilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Primary Accountabilities: Monitors aseptic techniques of personnel within the clean rooms. Monitors Outsourcing filling operations within the clean rooms. Verifies syringe filling rejects of Outsourcing products, as needed. etc. | 6/10/2020 |
| 10944 | Nephron West Columbia, SC Quality Assurance On Line Evening 12 hour Shift ONLY ( 6pm to 6:30am) HS diploma or equivalent Exp: 1-2 year(s) |
Position Summary: Performs Weight Check and Quality Attributes Inspection of the product through the filling and packaging process in compliance with company policies / procedures, FDA and cGMP regulations.H5 Ensures the accuracy and completeness of batch records. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. Primary Accountabilities: Monitors and perform start up, in-process and finished product inspections including weighing. Maintain quality assurance documentation. Promotes teamwork both within the QA Team and other departments. etc. | 6/10/2020 |
| 10945 | Nephron West Columbia, SC Microbiology Analyst I BS in biology, microbiology, or other life science Exp: 1+ year(s) |
Position Summary: Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Demonstrate high proficiency level on tests performed. Additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. The Primary Accountabilities and Knowledge, Skills and Abilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Primary Accountabilities: Apply quality scientific techniques in the microbiological analysis of raw materials; in-process & finished product samples to include: sterility, bioburden, identification, environmental monitoring, growth promotion, microbial recovery and media fill tests following approved procedures. etc. | 6/10/2020 |
| 10946 | Nitto Cincinnati, OH Research Scientist I MS in chemistry or related Exp: 1+ year(s) |
The Research Scientist I is responsible for executing analytical tasks, including method development activities, for one or more projects to support research and development primarily focused on oligonucleotides. Key Responsibilities: Execute testing per method or protocol for development, qualification, verification, validation, and transfer of analytical methods. Analyze test samples, process data, and report results with minimal errors to support research and development primarily focused on oligonucleotides. Provide analytical support to Process Development and Manufacturing. Design and perform method development experiments. Perform GDP and technical peer review. Author technical documentation (e.g. methods, procedures). etc. | 6/10/2020 |
| 10947 | Nitto Cincinnati, OH Quality Control Analyst I MS in analytical chemistry Exp: Not necessary for MS candidates |
Key Responsibilities: Provides analytical support to small molecule and oligonucleotide manufacturing groups utilizing various analytical instrumentation techniques including HPLC, UPLC, LCMS and NMR instrumentation. Records and reports results of analyses in accordance with prescribed lab procedures and SOPs. Maintains accurate and complete lab notebooks. Reviews laboratory documentation for calculation, entry and cGMP compliance. Develops and/or modifies test methods. Documents and reports results of development and experimentation in technical reports if needed. Participates in cGMP training and implements cGMP operating procedures. etc. | 6/10/2020 |
| 10948 | Nitto Marlborough, MA Research Scientist II/III MS Exp: 1-4+ year(s) |
The Research Scientist II/III is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. Design and execute testing per method or protocol for development, qualification, verification, validation, and transfer of analytical methods. Provide analytical support to Process Development and Manufacturing and help develop process controls. Analyze and review project data, correct errors, and report results. Design, review, perform, and improve method development experiments to support research and development primarily focused on oligonucleotides. Develop new analytical applications and technology. Perform GDP and technical review within multiple projects. etc. | 6/10/2020 |
| 10949 | Nkarta South San Francisco, CA Research Associate/ Senior Research Associate – Analytical Development BS/MS in immunology, cell biology, or related Exp: 1+ year(s) |
The Research Associate/ Senior Research Associate works closely with Process Development, Research and Quality groups towards in-depth characterization of the drug product. The primary goal is to design and develop assays to characterize the drug product. The design and development of release assays are also critical part of the assay development responsibilities. Key Responsibilities: Collaborates / leads analytical method development to enable the characterization, release and stability monitoring of our cell therapy drug product. Develops, improves and validates flow cytometry assays. Participates and/or performs method development activities for cellular cytotoxicity, ELISA, qPCR and other analytical assays for use in phase-appropriate product manufacturing. etc. | 6/10/2020 |
| 10950 | Noble Life Sciences Woodbine, MD Quality Assurance Officer BS/MS in a life science Exp: 1+ year(s) |
The QA Officer is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to Facility Manager and/or Sr. Vice President, Consulting Quality Assurance Unit. Responsibilities include but are not limited to: Become and maintain intimate familiarity with all applicable FDA and EPA GLP and other appropriate regulations and guidelines as well as with the company SOPs and other QA systems. Maintain a copy of the master schedule of GLP studies conducted at the testing facility. Review protocols for compliance to GLP regulations and NLS’s SOPs. Maintain copies of protocols for all GLP studies. etc. | 6/10/2020 |
| 10951 | Noble Life Sciences Woodbine, MD Quality Control Associate BS in a scientific discipline Exp: 1+ year(s) |
The QC Associate–is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to Sr. Vice President and a Consulting Quality Assurance Unit. Responsibilities include but are not limited to: Become and maintain intimate familiarity with all applicable FDA and EPA GLP and other appropriate regulations and guidelines as well as with the company SOPs and other QA systems. Supervise day to day quality control operations and documentation Assist in writing and reviewing standard operating procedures, study protocols and reports. etc. | 6/10/2020 |
| 10952 | Noble Life Sciences Woodbine, MD Animal Lab Tech BS in a scientific discipline Exp: 1+ year(s) |
The Animal Lab Tech–is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Vivarium Manager. Responsibilities include but are not limited to: Perform duties in accordance with relevant study protocols and the Standard Operating Procedures (SOPs). Follow and perform standard operating procedures (SOP) & Protocols on study and stock animals, including, but not limited to: clinical observations, food consumptions, body weights, urine collection, administering anesthesia, mating procedures, blood draws dose administration, restraint, euthanasia, catheter placement, feeding, food removal, on laboratory animals. Administer test and control articles or other substances (i.e. medications) to animals by various routes of administration. Collect blood samples from animals through various methods, process blood samples and collect bone marrow samples. etc. | 6/10/2020 |
| 10953 | Noble Life Sciences Woodbine, MD Animal Care Tech BS in a scientific discipline Exp: 1+ year(s) |
The Animal CareTech–is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Vivarium Manager. Responsibilities include but are not limited to: Read, understand and follow all SOP’s, Quality Assurance Standards and perform duties in accordance with the study protocol. Monitor daily animal health and wellness checks and report any abnormal animal conditions to the supervisor and/or the Study Director and record observations in appropriate logs. Ensure that all animals are fed the proper diet and have adequate water within the date and time requirements. Clean and disinfect animal holding rooms daily. etc. | 6/10/2020 |
| 10954 | Nordson Swainsboro, GA Machine Operator HS diploma or equivalent Exp: 1-2 year(s) |
Operates machine tools such as lathes, milling machines, finishing machines, and grinders, to machine parts by performing the following duties. Essential Job Duties and Responsibilities: Ability to read blueprints and drawings. Cleaning and basic maintenance of machines per TPM program. Knowledge of basic shop measuring techniques. Capable of de-burring parts. Capable of operating CNC machines by the loading and unloading of machines. Capable of performing basic QC checks. Follow all safety and housekeeping procedures. Conformance to production and administrative procedures. Enhancement of existing processes. etc. | 6/10/2020 |
| 10955 | Nordson Chippewa Falls, WI Manual Machine Operator (Super Finisher) - WKND Days HS diploma or equivalent Exp: 1-3 year(s) |
Operates machines or machining centers to perform various machine functions such as drilling, tapping, milling, reaming, and boring of work pieces. Essential Job Duties and Responsibilities: Read and interpret blueprints and can recognize when a blueprint may be incorrect. Start machine and monitor displays and machine operation to detect malfunctions. Manually adjust machine controls to correct malfunctions or out-of-tolerance machining. Operate machine manually to perform non-automated functions and when automatic programming is faulty or machine malfunctions. Discuss control media errors with supervisor to resolve problems. etc. | 6/10/2020 |
| 10956 | Nordson Salem, NH Production Associate I (Balloons) Third Shift Temp to Hire HS diploma or equivalent Exp: No experience required |
Position consists of manufacturing of medical components in a clean room environment while under general supervision in accordance with specifications and written procedures. This position may include machine operation, manual production using hand tools, visual inspection, physical measurements, and packaging of finished product. This position requires the ability to work with small and delicate components using a high degree of dexterity and accuracy. This position requires direct contact with medical grade components. Essential Job Duties and Responsibilities: Must be able to work under direct supervision and take work instruction from Supervisor and Leads, work cooperatively and productively within a team environment. etc. | 6/10/2020 |
| 10957 | Nordson Salem, NH Production Associate I (Shipping) First Shift Temp to Hire HS diploma or equivalent Exp: No experience required |
Position consists of manufacturing of medical components in a clean room environment while under general supervision in accordance with specifications and written procedures. This position may include machine operation, manual production using hand tools, visual inspection, physical measurements, and packaging of finished product. This position requires the ability to work with small and delicate components using a high degree of dexterity and accuracy. This position requires direct contact with medical grade components. Essential Job Duties and Responsibilities: Must be able to work under direct supervision and take work instruction from Supervisor and Leads, work cooperatively and productively within a team environment. Read, Understand and follow written procedures without deviating from the outlined process after training has been completed. etc. | 6/10/2020 |
| 10958 | Nordson Brooklyn Park, MN Production Operator II HS diploma or equivalent Exp: 6-12 month(s) |
Position consists of assembling and inspecting medical devices in a clean room environment while under general supervision in accordance with specific work instructions and SOPs. Assembly and inspection sometimes done under a microscope. This position requires the ability to work with small tools and assemble small components using a high degree of dexterity and accuracy. This position requires direct contact with an implantable medical device. Essential Job Duties and Responsibilities: Must be able to work under direct supervision and take work instruction from Supervisor and Leads, work cooperatively and productively within a team environment. Ability to do repetitive tasks, Detail-Oriented and adherence to Nordson’s Safety Policy. Read, Understand and follow Standard Operating Procedures without deviating from the outlined process after training has been completed. etc. | 6/10/2020 |
| 10959 | Nordson Norwich, CT Mold Maintenance Technician Trainee HS diploma or equivalent Exp: Not necessary |
Work independently and follow the overall work schedule, as determined by the department leader. Clean molds and complete mold changeovers to meet schedule requirements. ESSENTIAL DUTIES & RESPONSIBILITIES: Follow & update IQMS RT Scheduler mold requirements, as determined by the planner. Green-tag readied molds; move to staging area in molding department. Disassemble & clean molds; inspect for problems. Install changeover parts, as required. Other duties as assigned. Practice good housekeeping and appropriate measures to prevent pollution or other negative impacts on the environment. Work independently and follow the overall work schedule, as determined by the department leader. Clean molds and complete mold changeovers to meet schedule requirements. etc. | 6/10/2020 |
| 10960 | Novocure Portsmouth, NH Operations Support Specialist I HS diploma or equivalent Exp: 0-2 years |
The Operations Support Specialist I is responsible for organizing and ensuring the integrity of incoming and outgoing documentation that supports all key department processes. This position will be responsible for collaborating with and supporting internal and external customers. This is a full-time, non-exempt position reporting to the Supervisor, Operations Support and is based in Portsmouth, NH. Essential Duties & Responsibilities: Review Service Agreements. Perform error tracking and documentation. etc. | 6/10/2020 |
| 10961 | Nostrum Laboratories Kansas City, MO Packaging Technician HS diploma Exp: 1 year |
The Packaging Technician performs routine packaging operations for the production of pharmaceutical products; operates packaging line equipment according to established SOPs and department procedures. Duties and Responsibilities: Prepares and cleans room, equipment, facility and documents for manufacturing and packaging process. Verifies calculations, process steps and yield. Ensures that processes, tools, products and materials meet established quality standards and requirements. Notifies management when inventory fails below certain levels. Assists in the assembly and disassembly of process equipment as necessary. Examines sample of finished product per batch record instructions for conformance with specifications. etc. | 6/10/2020 |
| 10962 | Novartis Morris Plains, NJ Associate Scientist Bioanalytics BS in biology, chemistry, biochemistry, or related Exp: 1+ year(s) |
In the role of Associate Scientist Bioanalytics you will be responsible for performing Bio-Analytical testing such as Flow, ELISA, cell count, cell viability, residual bead assessment, qPCR. We are looking for an Associate Scientist who follows quality policies, work on shifts covering daytime / evening and one or both weekend days and execute method qualification/optimization of methods as per appropriate protocols. Your responsibilities include, but are not limited to: Contribute to OOS/OOE investigations and deviation investigations. Interface with regulatory agencies during audits. etc. | 6/10/2020 |
| 10963 | Novartis Johns Creek, GA Manufacturing Technician - Full Time Day & Night Shifts HS diploma/AS/AA Exp: No experience required |
Manufacturing Technicians participate in all aspects of production processes including but not limited to loading raw materials, operating SPC Lens Inspection, SAP final record review, operating secondary packaging equipment, performing lot changes, improving yields, using calibrated measurement equipment, troubleshooting and using support equipment such as sterilizers and tool drums. Interact closely with lens inspectors to identify defects and perform corrective actions as necessary. Perform minor equipment repairs and adjustments, and conduct Autonomous Maintenance and 5s duties. Coordinate downtime to ensure efficient use for maintenance, corrective actions, and cleaning. etc. | 6/10/2020 |
| 10964 | Novartis Carlsbad, CA Research Associate BS/BA Exp: No experience required |
Your responsibilities: Works in a GMP/GCP/GLP/CLIA regulated environment and is responsible for following all applicable regulations. Work in a regulated laboratory following work instructions and SOPs. Provide support for clinical assay development and/or validation activities. May assist in execution of routine testing for clinical specimens using established testing methodologies. Maintain accurate records related to all work with assay development, sample handling and testing, test and project results. Ensuring that Quality Events such as incidents and deviations are proper documented, and for supporting/owning the immediate remediation and preventative actions. Ensuring change requests are properly initiated, completed, and approved prior to the use of the assay, system, instrument, software, etc. being changed. etc. | 6/10/2020 |
| 10965 | Novartis Johns Creek, GA Lead Production Technician - LS1 Days HS diploma or equivalent Exp: No experience required |
Coordinate the shipment processes of a natural work area to achieve day to day goals in quality, service, and efficiencies. Actively participate on High Performance Teams to address day-to-day business activities, safety, quality, and training needs. Participate in meeting production goals/product quality. Assure that the goals for product volume and efficiencies are met by: Evaluating negative variances to plan using the MES system and other reports, document these and then determine action plan for correction. Performing shift cross-over w/counter-part at beginning and end of shift. Performing daily 5 minute meetings at the beginning of the shift with area personnel. etc. | 6/10/2020 |
| 10966 | Novartis Fort Worth, TX Technician III Packaging FWN CLC 1st shift HS diploma or equivalent Exp: 0-2 years |
Responsible of robust manufacturing process performed under current Good Manufacturing Practices (cGMP) and Health, Safety and Environment (HSE) and support the improvement of the process and deliver efficiency to full satisfaction of our customers. Contribute to maintain a high level of good housekeeping and carrying out operations within accepted GMP and HSE practices -Ensure proper escalation of all matters related with HSE, quality, supply and production, implement decisions and act as responsible for continuity of production -Support senior production operator with problem solving and teamwork and support a high performance teamwork environment. etc. | 6/10/2020 |
| 10967 | Novartis Houston, TX Molding Operator I HS diploma or equivalent Exp: No experience required |
Responsible for operating or monitoring tools and equipment on a daily basis used in the molding process. Operates light-duty bench or floor-type machine tools and equipment such as small lathes, power mills, extruding machines, drills or punch presses, power brakes, shears or saws. May set up machining machines and make adjustments, and perform maintenance on machines. Checks work using prescribed gauges, jigs and fixtures to measure close tolerances. Some machines may be numerically controlled. etc. | 6/10/2020 |
| 10968 | Novartis Fort Worth, TX Scientist (Pre-Clinical Development) BS/BA Exp: 0-1+ year(s) |
Conduct and maintain in vivo and in vitro exploratory and GLP-regulated preclinical safety studies in support of government submissions. Administers drugs to candidates via a variety of routes including topical ocular, intravitreal, intravenous, etc., to various test systems including nonhuman primates, rabbits, rodents, etc. Assists Study Directors and other senior personnel in the development and validation of new experimental methodologies. Follows study protocols; data will be generated and collected in an accurate and timely manner. Proofreads Data Packages for incorporation into technical reports, and are subject to audits by QAU and various regulatory agencies. etc. | 6/10/2020 |
| 10969 | Conformis Wilmington, MA Production Quality Engineer BS in engineering or sciences Exp: 1-3 years in QA/engineering |
Develop and maintain strong internal working relationships across Conformis. Understand the objectives, responsibilities, and mission of the Quality department and work towards those goals. Prioritize and plan work activities; adapt for changing conditions. Develops and initiates standard methods for inspection, testing, and evaluation, utilizing knowledge in related engineering fields. | 6/8/2020 |
| 10970 | Contract Pharmacal Corp Hauppauge, NY ENGINEER; VALIDATION MS in engineering Exp: 0-1 years in pharma/biotech/food |
The Validation Engineer is responsible for performing commissioning, qualification, validation (CQV) and engineering activities for solid dosage pharmaceutical manufacturing and packaging equipment, facilities and critical utility systems. Prepare and execute commissioning (URS, FAT, SAT) and qualification/validation (IQ, OQ, PQ) protocols/documents per required quality standards. Read, understand, verify and develop P&ID, engineering layout, engineering drawings and engineering documents. | 6/8/2020 |
| 10971 | Contract Pharmacal Corp Hauppauge, NY TECH I; PACKAGING SETUP (1st and 2nd Shift) HS Diploma/GED Exp: 1-2 years in as mechanical operators |
The Packaging Set Up Technician I: Primary responsibilities include set up various packaging equipment including but not limited to tablet fillers, bottle unscramblers and cleaners, cappers, cottoner, desiccant feeder, check weigher, metal detectors, labelers, cartoners, ink jet printers, etc. | 6/8/2020 |
| 10972 | Contract Pharmacal Corp Hauppauge, NY TECH; QA METROLOGY (Entry Level) BS/BA in sciences/engineering Exp: Entry Level |
The QA Metrology, Technician has primary responsibility for administering Laboratory computer programs such as Empower, managing the calibration and maintenance program for all laboratory equipment including related documentation such as SOPs and log books, and support the Data Integrity program. Complete all aspect of the company’s laboratory equipment and instrumentation program including; implementation, validation, periodic verification and calibration, perform basic troubleshoot etc. | 6/8/2020 |
| 10973 | Contract Pharmacal Corp Hauppauge, NY CHEMIST I; QC FINISHED PRODUCT & VALIDATION BS in chemistry Exp: 1 year in pharma lab |
A Chemist Level I is responsible for performing chemical testing and completion of real-time documentation per cGMPs and current SOPs. Perform UPLC, HPLC, GC, UV-vis, FTIR, ICP, TOC and wet chemistry testing . Proficient in various UPLC and HPLC software programs, such as Empower and EZ-Chrom. Assist in writing SOPs and Test Procedures following good documentation practice per company's SOP and cGMP regulations | 6/8/2020 |
| 10974 | Cook Group Boston, MA Field Based Service Technician - Northeast Region BS/BA Exp: 1-2 years |
The Field Based Service Technician located in Boston provides high quality, efficient and timely repair, preventative maintenance and installation of Cook capital equipment at customers' facilities to ensure that the equipment is performing in accordance with system requirements. Respond with limited notice to requests from within the territory, such as emergency service requests, preventative maintenance requests and/or installation requests | 6/8/2020 |
| 10975 | Cooper Surgical Group Guilford, CT Laboratory Technician BS in biological sciences Exp: 1-3 years in culture media |
We are seeking to hire an laboratory technician for full time employment in a large-scale culture media manufacturing facility. Candidate will be involved in a wide range of process tasks from maintaining an ISO certified cleanroom to final product. | 6/8/2020 |
| 10976 | Cooper Surgical Group San Antonio, TX Clinical Specialist BS/Ba Exp: 1-2 years in sales |
As a Clinical Specialist these goals and target accounts are set by both SBU Senior Management and the Regional Manager they are assigned to. Clinical Specialists will be responsible for supporting the sales of all SBU products where appropriate. Individual is required to make sales calls to surgeons of various specialties, operating room management, nursing, supply chain, and administration. | 6/8/2020 |
| 10977 | Corden Pharma Boulder, CO Manufacturing Process Technician HS Diploma/GED Exp: 0-2 years |
The Manufacturing Process Technician is responsible for the safe manufacture of pharmaceutical intermediates and API’s within one of the Corden Pharma Colorado Manufacturing Centers of Excellence. The Technician performs various unit operations on raw materials and intermediates according to written manufacturing procedures and SOPs. | 6/8/2020 |
| 10978 | Corden Pharma Boulder, CO Mechanical Tech I HS Diploma/GED Exp: 1 year in related |
Assists and performs predictive, preventive and corrective equipment maintenance for 24 hours/day, 7 days’/week bulk pharmaceutical manufacturing operation. Target to develop knowledge of site, equipment, and systems. This position is a developmental position, failure to adequately demonstrate growth in skills can lead to termination. | 6/8/2020 |
| 10979 | Corden Pharma Boulder, CO Materials Technician HS Diploma/GED Exp: 3 months in training/experience |
Serves as the detail facilitator for the movement to and from and daily usage of all materials in the Pharmaceutical manufacturing plants. Coordinates material requests from Line Management for the production batches with the Warehouse and Supply Planner and ensures the timely delivery of these materials to meet the production schedule. | 6/8/2020 |
| 10980 | Chem Pacific Baltimore, MD Chemist MS in chemistry Exp: 1 year |
Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. | 6/7/2020 |
| 10981 | Chiesia Cary, NC Regulatory Affairs Specialist 1-3, Labeling & Promotion BS in life sciences Exp: 1-3 years |
Responsible for managing the labeling control process, including generation of new labeling and changes to existing labeling, and submission of labeling information to regulatory authorities; and for the regulatory review and submission of advertising and promotional materials for all Chiesi USA products.а This position is also responsible for providing input to risk management activities. | 6/7/2020 |
| 10982 | Choice Spine Knoxville, TN Quality System / Document Control Specialist HS Diploma/GED Exp: 1-2 years in related |
Ensures compliance and timeliness, accuracy of routing and supportingdocumentation to specifications. Authorized to correct as necessary. Maintains the integrity of the document control system. Authorized to deny accessand to include, replace, revise or make obsolete documents therein. Has theresponsibility to confirm the accuracy of Work Instructions, Standard OperatingProcedures, Quality Reference Documents, forms and other documents againstspecifications whenever possible. | 6/7/2020 |
| 10983 | Choice Spine Knoxville, TN Quality Support HS Diploma/GED Exp: 0-2 years |
Supports Quality Inspection Department by completing visual and functional inspections ofMedical Devices. Under minimal supervision prints labels using ERP System. Packages andlabels medical devices and complete documents per Quality Management Systemsrequirements. Conduct visual and functional inspection of finished product for accuracy and adherence tospecifications. | 6/7/2020 |
| 10984 | Chrormatan Lower Gwynedd, PA ASSOCIATE SCIENTIST I BS in chemistry/biochemistry/chemical engineering Exp: 0-2 years industrial experience |
This position will support the downstream purification team for development and implementation of a fully integrated end to end continuous bio-production platform fully enabled with PAT. This position will focus on evaluating continuous operation technologies using quality by design techniques, to develop and optimize novel, continuous recovery and purification processes, for recombinant proteins and biological macromolecules. | 6/7/2020 |
| 10985 | Clinlogix Chicago, IL Clinical Research Associate BS/BA in life sciences Exp: 1-3 years in clinical research |
The Clinical Research Associate reports to and works under the direction of the Manager, Global Clinical Monitoring. Responsible to monitor clinical trials, study sites and clinical data while ensuring compliance with protocol and overall clinical objectives and Good Clinical Practice (GCP). Provides administrative and project support to clinical programs with minimum supervision. Interfaces with all project/clinical team members and off-site personnel as needed in support of project and departmental goals and responsibilities. | 6/7/2020 |
| 10986 | Coating Place Verona, WI QC Utility Operator HS Diploma/GED Exp: 1-3 years |
The primary purpose of the QC Utility Operator is to provide support to the Quality Control Department which includes EM Analysts, Analytical Chemists, Supervisors, Managers and the Director. This support is provided by ensuring the essential job functions of this position are completed as part of the daily and/or weekly schedule. | 6/7/2020 |
| 10987 | CODA Biotherapeutics San Francisco, CA Research Associate/Sr. Research Associate BS or MS in cell biology Exp: 1-2 years |
Design and validate cell-based fluorescence and automated electrophysiology assays to support receptor lead selection. Execute medium throughout compound screening and follow-up pharmacological evaluation of small molecules on lead chemogenetic receptors. Analyze and communicate data in written and oral modalities in both informal and formal settings. Generate and manage meticulous method protocols, data, and analysis reports in a clear and highly organized fashion. | 6/7/2020 |
| 10988 | Codexis Redwood City, CA Research Associate, Process Development-Downstream MS in chemical engineering/biochemistry Exp: 1-2 years in downstream processes |
The Process Development Associate will be responsible for the development, optimization, and scale-up of protein purification processes. The ideal candidate will have experience with the optimization of enzyme recovery/purification processes. Perform protein recovery experiments using unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration. | 6/7/2020 |
| 10989 | Cogmedix West Boylston, MA Assembly Technician I HS Diploma/GED Exp: 0-2 years |
Assemble subassemblies and final assemblies per written specifications i.e., work instructions, customer drawings, etc. Complete manufacturing documentation as outlined in the work order package and defined by the customer. Package final product per written specifications. Identify and report any product quality problems or discrepancies. | 6/7/2020 |
| 10990 | Cognito Therapeutics Cambridge, MA Engineer/Scientist BS/BA in sciences/engineering Exp: Junior level positions avalaible |
ou will apply your knowledge to the analysis of large, diverse data sets coming from our clinical and translational research studies. You will help us to develop our therapies and improve patient lives. Positions are available at junior and senior levels. Expertise in data analysis, signal processing, machine learning, statistics. Sound programming skills using data analyses languages (e.g. MATLAB, Python etc.) | 6/7/2020 |
| 10991 | Coloplast Coral Springs, FL Product Specialist HS Diploma/GED Exp: 1 year in contact center |
The Product Spercialist is a key driver of sales growth through the execution of inbound and outbound calls. The Representative achieves and exceeds annual sales objectives using outbound calling campaigns to introduce or re-introduce ostomy and continence products to consumers, will provide education about products that best fit the patient’s needs, troubleshoot product issues to gain end-user acceptance, and utilize the systems to document and route call for follow up. When applicable at the point of contact, respond appropriately to customers’ questions and resolve inquiries. | 6/7/2020 |
| 10992 | Coloplast Minneapolis, MN Pricing and Payments Associate BS or MBA in business/finance Exp: 0-2 years in analysis |
Analyze and model pricing scenarios for Integrated Delivery Network customers (IDNs), dealers and distributors for Requests for Proposal (RFPs). Devise customer incentives with the sales team that are in line with business objectives. Calculate monthly, quarterly, and annual payments for customers including national Group Purchasing Organizations (GPO), Health Systems (IDN), and Key Accounts as indicated by contractual commitments | 6/7/2020 |
| 10993 | Color Burlingame, CA Automation Engineer, R&D BS or M.Eng in electrical/mechanical/biotechnology engineering Exp: 0-2 years |
The ideal candidate approaches problems creatively and with eagerness; you have probably designed a Raspberry Pi controlled device to needlessly automate some aspect of your life, just because you thought it would be fun! We’d love you to join our R&D team, to design new hardware, to build automated products and to create the world's highest throughput and highest quality molecular biology automation stack. | 6/7/2020 |
| 10994 | Color Burlingame, CA Clinical Lab Assistant, COVID-19 (Temporary) BS/BA in sciences/engineering Exp: 0-2 years in CLIA-cert lab |
The Clinical Lab Assistant will be responsible for assisting in routine sample processing in a high complexity CLIA-certified laboratory, and you will be working with other laboratory professionals who have joined Color from UCSF, Stanford, Invitae, Counsyl, and other academic and commercial laboratories. Assist in routine laboratory maintenance, including equipment maintenance, maintaining lab cleanliness and a safe laboratory environment | 6/7/2020 |
| 10995 | Comet Therapeutics Cambridge, MA RA/Scientist/Sr. Scientist – cell biology BS or MS in biological sciences/engineering Exp: 1-3 years in pharma industry |
Tissue culturing of a variety of patient-derived as well as established cellular models. Transient and stable transfection, clonal cell line generation. Expand our understanding of disease biology, therapeutic MOA, biomarker development, andpatient impact. Deep bioanalytical characterization of cells, using a variety of methods | 6/7/2020 |
| 10996 | Complete Genomics San Jose, CA Research Associate BS/BA in life sciences Exp: 1-2 years in NGS |
Complete Genomics is looking for a Research Associate with a 6 month assignment with potential extension. The Research Associate will have the opportunity to engage in multidicisplinary projects for sequencing technology development. The position will play a key role in developing DNA/RNA libraries for the next generation sequencing. The successful candidate should have a keen desire to work at the bench. | 6/7/2020 |
| 10997 | Complete Genomics Houston, TX Field Application Scientist (Houston, TX) MS in life sciences Exp: 0-2 years |
Coordinate and conduct customer training for MGI NGS products and applications. Troubleshoot issues related to experimental design, data processing, software operation, sample preparation and chemical reaction. Perform preliminary on-site failure analysis to identify root cause and feedback to corresponding company department or personnel. | 6/7/2020 |
| 10998 | Complete Genomics Boston, MA Field Application Scientist MS in life sciences Exp: 0-2 years |
Coordinate and conduct customer training for MGI NGS products and applications. Troubleshoot issues related to experimental design, data processing, software operation, sample preparation and chemical reaction. Perform preliminary on-site failure analysis to identify root cause and feedback to corresponding company department or personnel. | 6/7/2020 |
| 10999 | Civetta Cambridge, MA Research Associate, Protein Biochemistry MS or BS in biological sciences Exp: 1-2 years in lab sciences |
Perform small-scale and pilot-scale expression trials using robotic liquid handling systems to identify conditions for soluble expression of human proteins in heterologous systems. Scale-up to liter volumes of bacteria in high-density bio-fermentation systems, and of insect cells in shaking incubators. Learn and implement standardized purification workflows for multiple-column purifications of fusion-tagged proteins | 6/7/2020 |
| 11000 | Civetta Cambridge, MA Research Associate, Molecular Biology MS or BS in biological sciences Exp: 1-2 years in lab sciences |
Assist in designing and creating expression vectors for use in bacterial and insect cell heterologous expression systems using robotic liquid handling systems. Perform small-scale and pilot-scale expression trials to identify conditions for soluble expression of human proteins in heterologous systems using robotic liquid handling systems. Scale-up to liter volumes of bacteria in high-density bio-fermentation systems, and of insect cells in shaking incubators | 6/7/2020 |
| 11001 | Concerto Remote/Memphis HQ, TN Quality Control (QC) Reviewer Associate's degree Exp: 0-2 years |
Concerto HealthAI is looking for a Quality Control (QC) Reviewer who will be responsible for reviewing and ascertaining the quality of curated data across the Data Curation Services (DCS) Division. The QC Reviewer works under the direct management of the Quality Control (QC) Manager. This role can be remote or based out of our Memphis office. | 6/7/2020 |
| 11002 | Concerto King of Prussia , PA Pharmaceutical Data Analyst – Analytics BS/BA in related Exp: 1-4 years in business/data analytics |
Writes and reads query language (specifically Microsoft SQL) for purposes of data management, data QC, reporting and analysis. Creates standard and custom reports that provide insight and value for clients using a combination of SQL, Excel, and BI tools. Evaluates internal data sources and processes for quality and integrity, working cross-functionally with other internal teams, Project Managers, and clients to resolve errors. | 6/7/2020 |
| 11003 | Concerto Memphis HQ, TN Data Abstractor Associate's degree Exp: 0-2 years |
Access electronic data systems for review of medical records and enter specific data into congruent electronic data systems. Review project specific documents, as needed, to develop familiarity with project goals and with the Abstractor tasks in each project. Use other resources as needed to gain the knowledge required to perform Abstractor work on new projects. | 6/7/2020 |
| 11004 | Clinilabs New York, NY Clinical Research Assistant/Medical Assistant (PER DIEM) – NY & NJ HS Diploma/GED Exp: 1-2 years |
The Research Assistant (RA) is responsible for assisting with document management, protocol related clinical assessments of research subjects, laboratory functions and assisting in tasks related to the work of the Clinical Research Coordinators. Assisting in subject visits, including direct contact with subjects, processing of visit data, ensuring the completeness and integrity of source documents and case report forms (CRFs), and other related duties. | 6/7/2020 |
| 11005 | Merieux Nutrisciences Burnaby, BC Laboratory Technician BS in chemistry, microbiology, or food science Exp: Not necessary for BS candidates |
We are looking for a Laboratory Technician in #106- 8255 North Fraser Way, Burnaby, B.C. V3N OB9 CAN. Your mission will be to: Provide basic assistance to the microbiology, wet chemistry, instrumental chemistry, sample preparation and maintenance operations of the laboratory. This position reports directly to the supervisor of the department in which they are working. Main activities: Prepare media, chemicals and reagents. Prepare, homogenize, weigh and perform simple extraction of samples. Provide routine sample analysis such as moisture, ash, pH, sensory, etc. etc. | 6/3/2020 |
| 11006 | Merieux Nutrisciences Dorval, QC Microbiology Technician AS/BS Exp: 0-1+ year(s) |
Prepare samples for processing and maintain documentation of processes to facilitate analysis procedures. Job Duties: Read plates and tubes, as required, to determine the number of organisms in the sample. Record findings on worksheet for verification. Write identification onto plates so that client and sample number can be tracked. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Prepare samples for analysis by recording, weighing, and blending. etc. | 6/3/2020 |
| 11007 | Merieux Nutrisciences Amarillo, TX Dairy Micro Technician AS/BS Exp: 0-1+ year(s) |
The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. Job Duties: Read plates and tubes, as required, to determine the number of organisms in the sample. Record findings on worksheet for verification. Write identification onto plates so that client and sample number can be tracked. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. etc. | 6/3/2020 |
| 11008 | Merieux Nutrisciences Gainesville, FL Chemist AS/BS Exp: 1-2 year(s) |
The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. Job Duties: Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. etc. | 6/3/2020 |
| 11009 | Merieux Nutrisciences Salida, CA Chem Tech AS/BS Exp: 0-1+ year(s) |
The incumbent is responsible for performing chemical analysis on food, pharmaceutical or other samples. Job Duties: Composting and grinding of samples for analysis as required. Perform chemical analyses such as protein, moisture, fat, ash, and other components. Prepare sample for analysis according to procedure. Retrieve samples from designated areas (e.g. log-in, sample storage). Perform chemical analyses of macronutrients, micronutrients or other parameters as designated. Extract desired component from sample with appropriate processes so that concentration can be determined. Prepare standards and reagents that are needed for the analysis procedure. etc. | 6/3/2020 |
| 11010 | Merieux Nutrisciences Allentown, PA Microbiologist I Unspecified Exp: 1-2 year(s) |
We are looking for a Microbiologist I. Responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. Follow appropriate methods and SOPS on all tasks. Maintain quality control records. Read, calculate, record data in Laboratory Information Management System. etc. | 6/3/2020 |
| 11011 | Merieux Nutrisciences Salida, CA Temp Lab Technician Unspecified Exp: Entry level |
Prepare samples for processing and maintains documentation of process to facilitate analysis procedures. This position requires weekend work. The Laboratory Technician we are looking for has… The ability to work collaboratively, as a member of a team, to achieve a common goal. A desire to protect themselves, their friends and family, and the entire world from illness caused by foodborne pathogens. The flexibility and productivity to work in a fast paced, often varied environment. A strong sense of pride in achieving accurate, timely, and consistent results in their work. etc. | 6/3/2020 |
| 11012 | MSD Gaithersburg, MD Research Associate I BS in life sciences, molecular biology, protein sciences or related Exp: 1+ year(s) |
A Research Associate I (RA I) is responsible for carrying out reagent and assay development activities in the laboratory, under supervision, working to achieve development project goals including data analysis and assay qualification. This is a laboratory position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). Some degree of professional latitude, creativity and self management is expected. DUTIES AND RESPONSIBILITIES: Analyze and prepare reagent and product documentation, organize and procure reagents, perform experiments, analyze data and document results. Presentation of results. etc. | 6/3/2020 |
| 11013 | Microspec Peterborough, NH Secondary Manufacturing Associate-All Shifts HS diploma or equivalent Exp: Entry level |
Secondary manufacturing to ensure on-time customer delivery and maintain healthy levels of customer stock. Essential functions of position (not limited to tasks listed): Loading and unloading of annealing ovens; Pulling mandrel from the product; Cutting the product to length; Marking of product for correct orientation; etc. | 6/3/2020 |
| 11014 | Moderna Cambridge, MA Research Associate, Quantitative Bioanalytics BS in biology, immunology, biochemistry, or related Exp: 1+ year(s) |
Reporting to the Director of Quantitative Bioanalytics, the Research Assistant will have a great opportunity to support platform development and non-clinical studies through the performance and development of laboratory-based assays for both mechanistic and quantitative assessment of novel therapies. The individual will work with scientists within the nonclinical group and other cross-functional groups to ensure the highest level of quality of these assays. The candidate must thrive in a fast pace environment with high expectations. Integrity, ability to share experimental issues and troubleshoot, curiosity, collaborative spirit, respect for people, exemplary work ethic and setting the bar high are key values to thrive in our Team. etc. | 6/3/2020 |
| 11015 | Moderna Cambridge, MA Research Associate, Respiratory Delivery BS Exp: 0-2 years |
This role is an exciting opportunity to be a critical part of a team enabling respiratory delivery of mRNA at an organization that is radically changing the biotech industry. We are seeking a Research Associate to support characterization of novel lipid nanoparticle formulations for delivery of mRNA. The position is primarily laboratory-based and offers the opportunity to develop a wide range of analytical skills and techniques within a fast-paced, dynamic, and highly interdisciplinary environment. Candidates with a foundation in chemistry, biochemistry, chemical engineering, biology, or a related field are encouraged to apply. etc. | 6/3/2020 |
| 11016 | Moderna Norwood, MA Sr./Research Associate, Process Development BS in chemical engineering, chemistry, biochemistry, or related Exp: 0-3 years |
The successful candidate must be able to work in a fast paced and highly dynamic environment, will have relevant academic and or industrial experience in large molecule bioprocessing, and will be able to contribute to both process development and commercialization related activities. We seek applicants that are proactive, enthusiastic, and show a passion for process development. Applicants should have exceptional time management and communications skills with a strong attention to detail. Previous experience with chromatography, nanoparticle formulations, filtration technologies, mixing technologies, and/or tangential flow filtration is preferred. The position will support cross-functional teams across CMC, Research and Development, Pre-clinical and GMP Production, Quality, and Analytical Development. etc. | 6/3/2020 |
| 11017 | Moderna Norwood, MA (Contract) Manufacturing Associate, 2nd Shift BS in biology, chemistry, chemical engineering, biomedical engineering or related Exp: Not necessary for BS candidates |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. etc. | 6/3/2020 |
| 11018 | Moderna Norwood, MA (Contract) Manufacturing Associate, 1st Shift BS in biology, chemistry, chemical engineering, biomedical engineering or related Exp: Not necessary for BS candidates |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. etc. | 6/3/2020 |
| 11019 | Moderna Norwood, MA Associate II, Quality Assurance BS in biology, chemistry, chemical engineering, biomedical engineering or related Exp: 0-2 years |
The individual in this role will be part of a cohesive team responsible for supporting cGMP mRNA drug products produced internally at Moderna. He/she will provide quality oversight and expertise to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will have experience in quality oversight or manufacturing experience in early stage clinical products. They will be able to interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Manufacturing, Logistical and Process Development Technology Transfer counterparts. etc. | 6/3/2020 |
| 11020 | Moderna Norwood, MA Associate I, Quality Control BA/BS Exp: 0-2 years |
Moderna is seeking Quality Control Associate I to be based at their Norwood, MA site. The individual in this role will perform cGMP QC release and stability testing and laboratory support functions. This individual may support special projects as assigned. This role will be assigned to the Wednesday to Saturday first shift (4 x 10hrs). Here’s What You’ll Do: Performs routine analytical or microbiology testing. Supports special projects as assigned. etc. | 6/3/2020 |
| 11021 | Molecular Templates Jersey City, NJ Clinical Trial Assistant BS in a life science Exp: 1+ year(s) |
Molecular Templates is seeking a highly-motivated and skilled professional to assist the Clinical Operations team. The Clinical Trial Assistant will provide support through maintenance of clinical trial studies. This includes establishing and maintaining the trial master file structure for all ongoing studies, providing coordination of supplies and inventory, coordinating meetings and preparing materials and ongoing general administrative support. This position requires excellent technical, analytical, time management and organizational skills, along with adherence to written and verbal instructions and accurate and timely completion of documentation. This position requires excellent organizational, time management and multi-tasking skills, along with the ability to follow standard operating procedures and manage competing priorities. etc. | 6/3/2020 |
| 11022 | MCRA Washington, DC Associate, Cardiovascular Regulatory Affairs BS/MS in a scientific discipline Exp: 1-3 year(s) |
The Associate, Cardiovascular Regulatory Affairs will be a critical team member reporting directly to the Associate Director, Cardiovascular Regulatory Affairs, to support regulatory strategy and submissions for the firm’s cardiovascular clientele. The majority of projects will initially be based around the following product types: stents, heart valves, circulatory support devices, intravascular catheters, etc., and we expect for this position to develop into supporting additional technological areas (i.e. electrical cardiology devices) and other growing therapeutic concentrations of MCRA. etc. | 6/3/2020 |
| 11023 | NAMSA Northwood, MA Animal Care Technician HS diploma or equivalent Exp: 0-2 years |
Principal Duties and Responsibilities: Primarily involved in the welfare and husbandry activities of animals, including sanitation of equipment and the vivarium. Receives, identifies, and acclimates laboratory animals. May euthanize animals. May administer medications under the direction of a Veterinarian. Follows the Quality Manual, all NAMSA SOPs, and Process documents. Documents all required tasks. etc. | 6/3/2020 |
| 11024 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - A Shift HS diploma or equivalent Exp: 3-12 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 6/2/2020 |
| 11025 | Mallinckrodt Pharmaceuticals Hobart, NY Manufacturing Assoc I - 3rd Shift HS diploma or equivalent Exp: 3-12 months |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. etc. | 6/2/2020 |
| 11026 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - D Shift HS diploma or equivalent Exp: 3-12 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 6/2/2020 |
| 11027 | Mallinckrodt Pharmaceuticals Hobart, NY Quality Control Lab Technician I - First Shift AS in chemistry, biology, or related Exp: 1 year |
Perform basic Wet Chemistry testing. Preparations of any and all solutions, solvents and mobile phases. Preparation of pharmaceutical components, in-process material, finished good product, and/or stability product samples for outside laboratory testing. Operation and maintenance of the dissolution and disintegration baths including the sampling of the dissolution baths and preparing the samples for quantitative analysis. Perform general cleaning to maintain the safety and overall cleanliness of the lab. Perform standard chemical and physical testing, such as weights, description verification, hardness, thickness, disintegration, friability and dispersion/ Perform using conventional and computerized equipment and work aids, and a variety of testing procedures. etc. | 6/2/2020 |
| 11028 | Mallinckrodt Pharmaceuticals Raleigh, NC Maintenance I/E Technician HS diploma/AS/AA Exp: 1-3 year(s) |
The Maintenance I/E Technician performs a variety of electrical and instrumentation duties involving the maintenance of plant facilities. S/he will be responsible for calibrating, installing, maintaining, repairing, and inspecting plant monitoring devices on a wide variety of complex digital, analog, programmable, and other auxiliary equipment. ESSENTIAL FUNCTIONS: Installs, troubleshoots, repairs, and calibrates low voltage AC/DC electrical and instrumentation controls as well as 3-phase 480-volt power circuits. etc. | 6/2/2020 |
| 11029 | Mallinckrodt Pharmaceuticals Hobart, NY Manufacturing Assoc I - 3rd Shift HS diploma or equivalent Exp: 3-12 months |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. etc. | 6/2/2020 |
| 11030 | Mallinckrodt Pharmaceuticals Hobart, NY Quality Control Tech I HS diploma/AS/BS in chemistry or biology Exp: 1-3 year(s) |
Perform basic, intermediate or advanced quantitative and qualitative analyses of pharmaceutical components, in-process material, finished good product, and/or stability product. Depending on the department to which the incumbent reports some of the functions listed may not be applicable. Job Results & Essential Functions: Perform basic analytical laboratory tests (such as potency, purity, uniformity, dissolution, moisture, etc.) in accordance with approved methodology and cGMP, FDA, and DEA regulations, including: Set-up, adjustment, calibration and operation of laboratory equipment and instruments, as well as any associated software. etc. | 6/2/2020 |
| 11031 | Masy Bioservices Pepperell, MA Calibration Field Technician II HS diploma/AS/AA Exp: 1-3 year(s) |
Perform routine calibration and preventive maintenance of Masy and customer equipment. Calibration may include temperature, relative humidity, CO2, voltage, pressure, time, rotation, etc. following documented procedures using precision standards. Calibrations will be performed in-house and at customer sites. Create, modify and execute calibration procedures and calibration certificates. Perform testing to support the quality management system and report, troubleshoot and make recommendations about quality issues relating to calibration. Assist in filing, data entry and general record keeping. etc. | 6/2/2020 |
| 11032 | Masy Bioservices Pepperell, MA Quality Associate I HS diploma or equivalent Exp: 1+ year(s) |
This position provides day to day support assisting in areas such as GMP, ISO 9001 and ISO 17025 compliance and the company’s quality system. Duties include quality assurance and control activities in technical, systems, operations and service areas. This position may require frequent interaction with multiple departments. Works under general supervision of management or team lead. Duties/responsibilities: Actively participate in Masy’s QMS to maintain GMP compliance, ISO 9001 certification and ISO 17025 accreditation consisting of two or more of the following areas: Perform quality review of calibration certificates before release to customers. etc. | 6/2/2020 |
| 11033 | McGuff Pharmaceuticals Santa Ana, CA Manufacturing Technician Unspecified Exp: Entry Level |
McGuff Pharmaceuticals, Inc. currently has an opening for a Manufacturing Technician within our production facility located in Santa Ana, CA. This position reports to the Production Supervisor. The candidate must be detail-oriented, results-oriented, possess good communication and writing skills, capable of performing assigned production duties and flexible in adapting to changing work priorities. Duties include: Operation of pharmaceutical manufacturing equipment including automated aseptic fill lines, washers, ovens, and autoclaves. etc. | 6/2/2020 |
| 11034 | McGuff Pharmaceuticals Santa Ana, CA Maintenance Technician / Mechanic Unspecified Exp: Entry Level |
McGuff Pharmaceuticals, Inc. currently has an opening for a Maintenance Technician/Mechanic within our production facility located in Santa Ana, CA. This position reports to the Production Supervisor. The candidate must be detail-oriented, results-oriented, possess good communication and writing skills, capable of performing assigned production duties and flexible in adapting to changing work priorities. Duties include: Maintain production equipment by providing troubleshooting, including adjusting, repairing, and replacing components to ensure equipment performance is reliable and meets expectations. etc. | 6/2/2020 |
| 11035 | MDx Health Irvine, CA Product Development Associate MS Exp: 0-3 years |
The Product Development Associate is involved in assisting with the planning, conducting and analyzing experiments leading to validation of diagnostic tests in the field of oncology. The PD Associate works in a team and needs to communicate relevant information to professional colleagues and to participate constructively in discussions that will impact the performances of the final product. etc. | 6/2/2020 |
| 11036 | MDx Health Irvine, CA Specimen Accessioner I Unspecified Exp: 1-2 year(s) |
The Specimen Accessioner I performs all paperwork and non-technical procedures required to prepare, process, and submit specimens to the laboratory for testing. Responsibilities will include but not limited to: receiving, triaging and accessioning patient samples, distribution of patient reports and specimens to clients, performing quality control of accessions and labeling. etc. | 6/2/2020 |
| 11037 | Cook Group Boston, MA Field Based Service Technician - Northeast Region BS in electronics or biotechnology Exp: Not necessary for BS candidates |
The Field Based Service Technician located in Boston provides high quality, efficient and timely repair, preventative maintenance and installation of Cook capital equipment at customers' facilities to ensure that the equipment is performing in accordance with system requirements. Responsibilities: Read, understand, and carry out written and oral instructions. Read from simple to complex drawings to build and repair equipment. Perform scheduled maintenance on field based installed equipment. etc. | 6/2/2020 |
| 11038 | Medicomp San Francisco, CA Cardiac Monitoring Technician - San Francisco HS diploma Exp: 1+ year(s) |
Looking for an ECG interpreter, for our San Francisco, CA office, who is excited about having the front line responsibility of triaging the patients who have our life-saving products prescribed to them. That's right, I said Life-saving! This is only going to happen one way you have to have a solid work ethic and be able to focus on the clinically significant signs and symptoms of one or more patients while in a noisy environment that is full of interruptions. Receiving ambulatory ECG data from phone and web transmissions. Making the correct arrhythmia call, not just knowing where to place the electrodes. Phone interaction with cardiac patients for the majority of your shift. etc. | 6/2/2020 |
| 11039 | Cantel Medical Plymouth, MN Applications Engineer Technical degree Exp: 0-2+ years |
At Cantel, preventing infection is our business. As a leading provider of infection prevention products and services in the healthcare market, we are dedicated to delivering high-quality, innovative solutions that improve outcomes and help save lives. We accomplish this mission by delivering our products through the following operating units: Medical: Endoscopy procedure disposables include single-use valves and irrigation tubing. The medical device reprocessing systems, disinfectants, detergents we manufacture and distribute are used to disinfect high-level endoscopes. etc. | 6/2/2020 |
| 11040 | LabCorp Overland Park, KS Specimen Processor HS diploma or equivalent Exp: 1-2 year(s) |
Job Duties/Responsibilities: Prepare laboratory specimens for analysis and testing. Unpack and route specimens to their respective staging areas. Accurately Identify and label specimens. Pack and ship specimens to proper testing facilities. Meet department activity and production goals. Properly prepare and store excess specimen samples. etc. | 6/2/2020 |
| 11041 | Meridian Bioscience Cincinnati, OH Machine Operator- Entry Level HS diploma or equivalent Exp: Entry level |
The Machine Operator (ImmunoCard Operator I) safely manufactures FDA regulated medical devices in a fast-paced and results-oriented environment, meeting quality standards in accordance with cost, schedule and all standard cGMP operating procedures and guidelines. KEY DUTIES: Perform manual and automated assembly/packaging of commercial diagnostic products. Operate and maintain automated production equipment. etc. | 6/2/2020 |
| 11042 | Meridian Bioscience Cincinnati, OH Regulatory Affairs Associate BS in biological science, microbiology, chemistry or related Exp: 1+ year(s) |
This position will be responsible for supporting Meridian’s regulatory and quality processes and ensuring that Meridian’s activities are consistent with applicable quality and regulatory requirements. Assist with product compliance throughout all stages of the product lifecycle as well as work with cross-functional teams to provide support of business objectives. Also assist in assembling timely preparation of documents for domestic and international regulatory submissions, ensuring compliance with applicable regulations. etc. | 6/2/2020 |
| 11043 | Meridian Bioscience Cincinnati, OH Production Worker- Entry Level HS diploma or equivalent Exp: Entry level |
The Production Worker (Para-Pak Operator I) safely manufactures FDA regulated medical devices in a fast-paced and results-oriented environment, meeting quality standards in accordance with cost, schedule and all standard cGMP operating procedures and guidelines. Key Duties: Operate manual and automated assembly/packaging of commercial diagnostic products. etc. | 6/2/2020 |
| 11044 | Mammoth Biosciences San Francisco, CA Research Associate - Sample Prep BS/MS in biology, chemistry, or related Exp: 1+ year(s) |
Mammoth is seeking a Research Associate experienced in protein and nucleic acid biochemistry techniques to support our research and product development teams. The ideal candidate will have experience with in vitro assay development, nucleic acid extraction and amplification techniques. Further, the candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. Responsibilities: Assist in developing, validating, and improving CRISPR-diagnostic assays. etc. | 6/2/2020 |
| 11045 | CelSci Vienna, VA Assistant/Associate Immunologist I BS/BA in related Exp: 0-2 years |
The Assistant/Associate Immunologist will assist in the day-to-day activities related to the QC testing of Leukocyte Interleukin, Injection (LI) under current Good Manufacturing Practices (cGMP) for clinical application, and QC equipment/facilities operations and maintenance. Quality Control testing of all GMP Manufacturing samples (ELISA, pH, visual inspection) | 5/31/2020 |
| 11046 | CelSci Vienna, VA Manufacturing Support Technician AA degree in related Exp: 1+ years |
The Support Technician contributes to the manufacturing team effort by accomplishing related tasks and assignments. Understanding and awareness of current Good Manufacturing Practices. (cGMP) and basic familiarity with FDA and EU Guidelines. Able to follow Standard Operating Procedures (SOP’s). | 5/31/2020 |
| 11047 | Cepheid Sunnyvale, CA QC Analyst II AA or technical trade degree Exp: 1-2 years |
The Quality Control Analyst II will perform qualification and manufacturing of template materials used in internal product testing and as raw materials for production according to established procedures. This position will be working in Quality Control to support control reference material production as well as stability program activities in accordance to GMP standards and FDA/ISO regulations. | 5/31/2020 |
| 11048 | Cepheid Lodi, CA ME Technician I HS Diploma/GED Exp: 1-2 years |
Lifts and installs specified molds into molding machines. Bolts molds in position, adjusts mold height and sets ejector stroke for a wide range of Molding Presses. (set up. Ability to set / select the molding conditions, processes or programming for Molds at the right press. Proficient with all auxiliary equipment, Chillers, Mold Heaters, Conveyors and Yushin Robots. | 5/31/2020 |
| 11049 | Charles River Malvern, PA Technician 1 Mammalian Cell Banking BS/BA in sciences Exp: 0-2 years in lab |
The responsibilities of this role as Technician 1 Mammalian Cell Banking will be specific to the Mammalian Cell Banking division of the Manufacturing Services department. Expand and harvest a mammalian cell line to generate several hundred vials of a Cell Bank. Work within a clean room suite while gowned in clean room attire. | 5/31/2020 |
| 11050 | Charles River Mattawan, MI Research Technician- Safety Pharmacology BS or MS Exp: 0 years required |
A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 5/31/2020 |
| 11051 | Charles River Reno, NV Lab Assistant 1 (Laboratory Sciences) HS Diploma/GED Exp: 0 years required |
Performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. | 5/31/2020 |
| 11052 | Charles River Ashland, OH Research Technician 1 HS Diploma/GED Exp: 6-12 months |
The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical obsercations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 5/31/2020 |
| 11053 | Charles River Ashland, OH Research Technician I, Technical Operations HS Diploma/GED or BS in life sciences Exp: 0 years required |
We are seeking Research Technicians for our Safety Assessment site located in Ashland, OH. Charles River Ashland is growing and we're seeking motivated individuals to join our team! Extensive on the job training is provided with no prior experience necessary. If you have an interest working with animals and desire a fast paced work environment with tons of opportunity this may be a career for you. | 5/31/2020 |
| 11054 | Charles River Malvern, PA Technician 1 Cell Bank Manufacturing BS/BA in sciences Exp: 0-2 yearas in biological lab |
The responsibilities of this role as Technician 1 Cell Bank Manufacturing will be specific to the Microbial Cell Banking division of the Manufacturing Services department. Daily activities and responsibilities of this role will include, but are not limited to the following: Expand and harvest a microbial cell line to generate several hundred vials of a Cell Bank. Work within a clean room suite while gowned in clean room attire. | 5/31/2020 |
| 11055 | Charles River Spencerville, OH Research Technician I HS Diploma/GED or BS in life sciences Exp: 6-12 months |
The Research Technician will collect and record data with minimal supervision in the performance of studies. During a typical day, you can expect to perform clinical observations, sample collection, monitoring of food consumption, animal husbandry, and accurate data collection and reporting, along with the handling and restraint of animals. | 5/31/2020 |
| 11056 | Sanofi Framingham, MA Manufacturing Specialist I BS/BA Exp: 1-3 years |
The Manufacturing Specialist I uses expert knowledge of compliance and GXP manufacturing processes to manage investigation and improvement initiatives within manufacturing operations. Participates on cross functional teams to drive complex investigation close outs, determine root cause and implement appropriate Corrective and Preventative Action. | 5/31/2020 |
| 11057 | Sanofi Framingham, MA Manufacturing Associate BS/BA Exp: 1 year relevant experience |
The candidate for this full-time position will work as part of a team to perform the protein purification manufacturing processes in a multiple product pilot facility in a regulated cGMP environment as follows: Following good documentation practices and strict adherence to SOPs and batch records is required. Operate downstream purification equipment for chromatography, nanofiltration and tangential flow filtration. | 5/31/2020 |
| 11058 | Sanofi Ridgefield, NJ Aseptic Technician Associate HS Diploma/GED Exp: 1-3 years in cGMP environment |
Independently performs the tasks of the production operation specific to aseptic manufacturing, filling, and packaging. Maintains batch record documentation and logs as required by corporation and regulatory agencies. Performs cleaning and sanitizing of production equipment and classified production space. Prepares equipment, glassware, filters, etc. required for production. Assists in process and system validation activities as required. | 5/31/2020 |
| 11059 | Sanofi Framingham, MA Research Associate MS in biological sciences Exp: 0-2 years in cell culture |
Responsibilities will include expression vector construction; generation and evaluation of cell lines, including genetic characterization, conducting studies to improve recombinant protein expression and cell line development platforms; development of novel methods for cell line characterization and formal documentation of associated procedures. Manage work assignments, analyze and interpret test results, and conduct necessary troubleshooting; consult with supervisor as needed. | 5/31/2020 |
| 11060 | Sanofi Swiftwater, PA Production Technician BS/BA Exp: 0 years in cGMP or pharma |
Performs production in accordance with volume fluctuation, business need, and effective procedures. Must be flexible to ensure staffing for changing business volume and needs. Works with Senior Technicians, leads, and managers to ensure operational area is running as intended to meet all operational goals. Must attend shift change daily to ensure preparedness for workday. | 5/31/2020 |
| 11061 | Baxter Marion, NC Quality Lab Assoc I BS/BA in biological sciences Exp: 0-2 years |
Conduct microbiological analyses on raw materials, in-process and finished products. Collect samples related to Environmental Monitoring program at Baxter manufacturing area. Work under minimum supervision. Use laboratory instrumentation and computer systems to collect and record data. | 5/31/2020 |
| 11062 | Baxter Round Lake, IL Quality Lab Associate I BS/BA in biological sciences Exp: 0-2 years |
Conduct biological, chemical and physical analyses on pharmaceutical products (biologic and drugs) and medical devices through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs Conduct critical biological, physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities | 5/31/2020 |
| 11063 | ChemBio Medford, NY Production Technician Level 1 BS/BA or Associates in biology Exp: 0-2 years |
Under direct supervision, the Production Technician Level 1 is responsible for the preparation and application of components used to produce Chembio diagnostic products. Responsible for the application of all buffers, test lines, control lines, and other components used in Chembio diagnostic products. | 5/31/2020 |
| 11064 | ChemBio Medford, NY Quality Control Laboratory Analyst BS in biological sciences Exp: 1-3 years in cGMP environment |
Responsible for execution of analytical laboratory tests and evaluations of product performance and processes in the Quality Control Department, in accordance with approved methodologies, policies, and associated regulations. Performing analytical laboratory tests applied by the QC Laboratory for evaluation of raw materials, components, and products at various stages of the manufacturing process. | 5/31/2020 |
| 11065 | Cepheid Sunnyvale, CA Facility Technician HS Diploma/GED Exp: 0-1 years in facilities |
The primary function of the M.A.C. Coordinator is the scheduling and implementation of Moves, Adds and Changes from work orders provided by Space Planning. The space planning list will contain the names and destination locations for upcoming new hires as well as those of internal move requests. The M.A.C. Coordinator will reach out to the end user to schedule the implementation. Requests will range from individual staff relocation to furniture systems reconfiguration. | 5/31/2020 |
| 11066 | Cepheid Sunnyvale, CA Associate Scientist - Infectious Disease MS in field Exp: 0-2 years |
Perform analytical studies to verify GeneXpert assay performance based on the ability to meet design input requirements. Analyze data using statistical tools such as Microsoft Excel or MiniTab. Handle clinical samples and perform microbiology work of BSL-1 and BSL-2 organisms. Demonstrated ability to apply analytical problem-solving skills to reagent and system integration issues to identify critical performance factors. | 5/31/2020 |
| 11067 | Cepheid Lodi, CA Manufacturing Technical Trainer HS Diploma or AA/Trade Degree Exp: HS: 1-2 years, AA: 0-1 years |
Assist Supervisors/Training Specialists in coordinating, delivering, and monitoring training activities that directly affect manufacturing processes, including QSR/GMP compliance. Facilitate and deliver classroom training sessions. Serve as the point of contact for specific learning programs, as assigned. | 5/31/2020 |
| 11068 | Cepheid Sunnyvale, CA Associate Scientist BS or MS in biological sciences Exp: 1-2 years in devices/pharma |
This position is in the Biotechnology R&D group and is primarily a bench level job focusing on real time PCR and RT-PCR assay and product development in an FDA-QSR and ISO9001 compliant organization. The candidate will plan and execute laboratory research, demonstrate appropriate technical proficiency, scientific creativity and collaboration with cross-functional departments. | 5/31/2020 |
| 11069 | Celsee Ann Arbor, MI Laboratory Research Technician BS in biology/biochemistry Exp: 1-2 years lab experience |
The Laboratory Research Technician will work under the guided supervision of an interdisciplinary team of biologists and engineers to validate molecular assays on single-cells. The job responsibilities include: Performing various standard laboratory assays including NGS, Library Prep, PCR, Cell capture and analysis on Celsee’s proprietary devices. | 5/31/2020 |
| 11070 | CareDx Brisbane, CA Clinical Laboratory Assistant (Wed-Sat 9:00PM-7:30AM) AA or BS/BA in biological sciences Exp: 1-3 years |
The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed. | 5/30/2020 |
| 11071 | CareDx Brisbane, CA Clinical Laboratory Assistant AA or BS/BA in biological sciences Exp: 1-3 years |
(Tuesday through Friday 7:00 AM - 3:30 PM and Saturday 9:00am-5:30pm) Receive and record samples into the laboratory information management system (LIMS) to facilitate sample throughput. Data entry of patient and customer data. Perform patient specimen processing under the direct and constant supervision of a licensed CLS. | 5/30/2020 |
| 11072 | CareDx Brisbane, CA Patient Care Manager I BS/BA in health sciences Exp: 1-3 years |
Be a "Jack/Jane of all trades" and possess a wealth of cross functional knowledge including operational, clinical, and reimbursement. Contact centers and work with center personnel to ensure orders for patient tests are complete (50 %). Liaise between customers and cross-functional internal teams, ensure the timely and successful delivery of our solutions | 5/30/2020 |
| 11073 | CareDx Brisbane, CA Patient Care Manager I BS/BA in health sciences Exp: 1-3 years |
Be a "Jack/Jane of all trades" and possess a wealth of cross functional knowledge including operational, clinical, and reimbursement. Contact centers and work with center personnel to ensure orders for patient tests are complete (50 %). Liaise between customers and cross-functional internal teams, ensure the timely and successful delivery of our solutions | 5/30/2020 |
| 11074 | CRISPR Theraputics Cambridge, MA Research Associate II, Analytical Development MS in life sciences Exp: 0-2 years in assay development |
The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. | 5/30/2020 |
| 11075 | CRISPR Theraputics Cambridge, MA Cell Bank Research Associate II, Analytical Development MS in life sciences Exp: 0-2 years in assay development |
The individual will be responsible for isolating primary cells from donor samples, developing quantitative assays for measuring consistency across donors, and screening donors to ensure reproducibility across cell-based assay runs. The successful candidate will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work independently to support process development and product characterization. | 5/30/2020 |
| 11076 | CRISPR Theraputics Cambridge, MA Bioinformatics Engineer MS in computer/biological sciences Exp: 0-2 years |
We are seeking a talented Bioinformatics Engineer with strong programming skills to tackle challenging bioinformatics and computational biology problems. The successful candidate work collaboratively with research groups to build and maintain the tools, algorithms, and pipelines required to support the development of new, transformative CRISPR/Cas9-based gene editing therapies. | 5/30/2020 |
| 11077 | CRISPR Theraputics Cambridge, MA Research Associate II/Senior Research Associate, Editing Technologies - Cellular Biology MS in biology Exp: 1 year research experience |
Implement multiplexed gene editing strategies for next-generation CRISPR-based therapies. Engineer mammalian cells with CRISPR/Cas9, and perform downstream molecular and cellular analysis. Culture mammalian primary cells and cells lines, and introduce plasmid DNA, mRNA, gRNA and Cas9 RNP by appropriate methods, including cationic lipid-based transfection and electroporation. | 5/30/2020 |
| 11078 | Casmaniacs Cambridge, MA Research Associate, Biology MS in biological sciences Exp: 1-3 years in research sciences |
Cell culture and cell line development using retro- and lenti-virus, CRISPR and downstream analysis of autophagy and signaling. Perform western blotting, FACS and imaging analysis to analyze autophagy and specific target activity in primary cells and cell lines. Aid in conducting genome-wide CRISPR screens for novel target ID. | 5/30/2020 |
| 11079 | Catalent Winchester, KY Process Engineer BS in mechanical, Chemical or Electrical Engineering Exp: 0-2 years |
The Process Engineer is a member of the Site Engineering Team. This team drives the process and equipment improvement agenda as well as root cause analysis around process-oriented deviations for site operations. Evaluate and prioritize capital projects to improve site performance, efficiency, safety, quality and cost. Collaborate with key stakeholders, customers, suppliers and peers to identify all project requirements | 5/30/2020 |
| 11080 | Catalent Baltimore, MD Process Engineer I MS in Chemical Engineering, Chemistry, Biochemistry, Life Sciences Exp: 1-3 years |
Expands the technical capabilities of Process Development group, such as technology development, use of the literature and systems development. Assists in moving projects forward toward GMP Manufacturing for clinical trials, registration, or improvements of existing processes and products. Executes on project work including: Primary recovery from cell paste or inclusion bodies of specific proteins/macromolecules, Downstream processing of macromolecules expressed in mammalian cell lines, insect cells, or microbes, Development and execution of purification and analytical protocols. | 5/30/2020 |
| 11081 | Catalent San Diego, CA Preform Chemist I BS in biological sciences Exp: 0-2 years in preformulation |
Duties may include the preparation of simple aqueous and organic buffered solutions, volumetric dilution of samples and standards using good laboratory techniques, clear and accurate record keeping in laboratory notebooks, use of analytical instrumentation to acquire raw data, calculation and reporting of final results. | 5/30/2020 |
| 11082 | Catalent Harmans, MD Associate Automation Engineer BS in engineering Exp: 0-3 years in automation role |
The Associate Automation Engineer will provide key support for various manufacturing, quality and research systems. This will include Programmable Logic controllers (PLC), OSI-PI for Data Historian, IGNITION for data reporting & remote alarms, process equipment such as Single-Use (SU) Bioreactors, SU Chromatography Purification & Filtration systems, and Other Equipment Manufacturer (OEM) systems in Manufacturing, QC labs and Research Operations. | 5/30/2020 |
| 11083 | Catalent San Diego, CA Analytical Chemist I BS in physical/chemical/biological sciences Exp: 0 to 2 years of experience in analytical development |
The Analytical Chemist I will be expected to understand and execute basic analytical procedures in order to assess the quality of pharmaceutical API, intermediates, and final drug products under limited supervision. Duties may include the preparation of simple aqueous and organic buffered solutions, volumetric dilution of samples and standards using good laboratory techniques, clear and accurate record keeping in laboratory notebooks, use of analytical instrumentation to acquire raw data, calculation and reporting of final results. | 5/30/2020 |
| 11084 | Catalent Harmans, MD Manufacturing Associate I, Downstream Associate’s Degree in a scientific, engineering or biotechnology Exp: 0-2 years related experience |
The Manufacturing Associate I Downstream is responsible for supporting the overall GMP downstream manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II & commercial GMP manufacturing. | 5/30/2020 |
| 11085 | Catalent Madison, WI Associate 1, Biomanufacturing B.S./B.A. in Biotechnology Exp: 0 years required |
Perform aseptic techniques within in a clean room environment. Operate cGMP Biomanufacturing equipment such as pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Execute and document cGMP Biomanufacturing activities | 5/30/2020 |
| 11086 | Celgene Seattle, WA Research Associate, Viral Vector Process Development Exp: |
The Research Associate will join our viral vector process development group supporting process development, production and characterization of viral vectors, which are key intermediates in the CAR-T drug product. The candidate will support current programs and advance our capabilities in vector production. | 5/30/2020 |
| 11087 | Cellink Boston, MA Technical Support Specialist BS in mechanical, software, or electrical engineering Exp: 0-3 years |
Provide high level technical support to CELLINK customers for a wide range of products. Diagnose, troubleshoot and resolve hardware and software questions from customers and create trouble tickets for hardware and software issues. Remotely interface, troubleshoot, diagnose and repair customer equipment supporting end customers, Application Specialist Team and distributors worldwide. | 5/30/2020 |
| 11088 | Cello Health Florham Park, NJ Research Analyst BS or MS in sciences or engineering Exp: 1-3 years |
Support the consulting staff on projects across all therapeutic categories and providing the staff with broad experience in a wide range of indications. Perform the secondary research and data analyses that provide the foundation for our commercial assessment, search, and strategy projects. Drug pipeline and clinical trial analyses, indication or company profiling, deal and trend analyses, and literature searches to support findings from the primary research | 5/30/2020 |
| 11089 | Cello Health Florham Park, NJ Research Analyst MS in sciences or engineering Exp: Entry Level |
As an Associate Consultant, you will work as a member of project teams performing commercial assessments of development-stage pharmaceutical products and technologies including forecasting, market and pipeline analyses, identification and evaluation of licensing and partnering opportunities, and development of clinical and commercial positioning strategies. | 5/30/2020 |
| 11090 | Capricor Beverly Hills, CA Process Development Associate MS in sciences Exp: 0-2 years |
Independently manage and maintain multiple cell lines in support of process development activities. Design and execute studies to develop and optimize a scalable manufacturing process and analytical assays for production, isolation and characterization of exosomes. Prepare technical summaries to disseminate study results including making detailed observationsand data collection and analysis | 5/30/2020 |
| 11091 | Celerion Lincoln, NE Sample Management Technician HS Diploma/GED, Associates preferred Exp: 0-2 years |
Receive and check-in biological samples. Complete all record-keeping required for check-in, samples transfer log for chain of custody and freezer log. Communicate with client or sites as required for sample coordination. Manual entry of sample data | 5/30/2020 |
| 11092 | Fujifilm Cellular Dynamics Madison, WI Laboratory Technician (#322) Associate’s Degree in a scientific, engineering or biotechnology Exp: 1-2 years |
FUJIFILM Cellular Dynamics, Inc is recruiting for a laboratory technician to work in our cell manufacturing and research facility in Madison, WI. Provide lab support for scientific personnel and overall operations. Place orders, maintain inventory, and stock laboratory supplies. Work with laboratory staff to maintain and mature organizational structure. | 5/30/2020 |
| 11093 | Cellectis Raleigh, NC QC Raw Materials Analyst BS in life/analyatical sciences Exp: 1-3 years in lab |
Ensure compliance with applicable US and European cGMP regulations, corporate policies and company Standard Operating Procedures. Perform cGMP sampling, inspections, distribution of samples, and testing on raw materials and consumables. Review and evaluate timely issuance, review and approval of Raw Material testing results | 5/30/2020 |
| 11094 | Cellectis New York, NY Research Associate, Immunology BS or MS in biological sciences Exp: 1 year lab experience |
Design, set up, perform and analyze experiments independently. Maintain cell cultures and perform cell-based and immunological assays (e.g. ELISA, Cytotoxicity, proliferation, apoptosis). Evaluate novel cellular therapies using cellular and molecular biology techniques. Perform and analyze multicolor flow cytometry experiments. | 5/30/2020 |
| 11095 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Inspection Technician HS diploma or equivalent Exp: 0-2 year(s) |
We are looking for multiple Drug Product Inspection Technicians for 1st and 2nd shifts. In this role you will be responsible for performing a wide variety of product inspection and packaging tasks. You will complete training and pass qualification testing for visual inspection of various product forms, perform accurate visual inspection and handling of products following SOPs while working under cGMP regulations. Please Note: 1st shift hours are 6:30 - 3:00 pm and 2nd shift hours are 3:00 - 11:30 pm. etc. | 5/27/2020 |
| 11096 | Ajinomoto Bio-Pharma Services San Diego, CA Manufacturing Quality Assistant HS diploma/BS in a life science Exp: 0-2 year(s) |
Ajinomoto Bio-Pharma Services is currently seeking a MQA Assistant to support our manufacturing. The MQA Assistant ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. This individual has the ability to work independently, within prescribed guidelines, and as a team member. This position promotes a cGMP environment and follows SOPs. Responsibilities: Performs cGMP documentation/data review in support of manufacturing operations (e.g. logbooks, labels, etc.). Performs AQL inspection of final filled product. etc. | 5/27/2020 |
| 11097 | Ajinomoto Bio-Pharma Services San Diego, CA Environmental Monitoring Assistant HS diploma/BS in a life science Exp: 0-2 year(s) |
We are looking for an Environmental Monitoring Assistant to support Ajinomoto Bio-Pharma Services’ manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. Responsibilities : Performs environmental monitoring within the microbiology laboratory, manufacturing suites, clean rooms, and drug product operations. Performs enumeration and gram staining of bacterial colonies. etc. | 5/27/2020 |
| 11098 | Akorn Somerset, NJ Sanitization Associate I HS diploma or equivalent Exp: 1 year |
All Sanitization Associates are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. ESSENTIAL FUNCTIONS: Include the following. Other duties may be assigned. Compliance with associated SOPs and training requirements. Removal of used scrubs and coveralls into appropriate bins. Stocking of consumable items, such as bouffant hats and beard covers. Stocking of sterile and non-sterile gowns. Transport supplies into controlled areas from warehouse. Disposal of controlled area trash into appropriate bins. etc. | 5/27/2020 |
| 11099 | Akorn Somerset, NJ Sanitization Associate 6 pm - 2:30 am HS diploma or equivalent Exp: 1 year |
All Sanitization Associates are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. ESSENTIAL FUNCTIONS: Cleaning and sanitizing aseptic production areas. Set up/preparation/cleaning and autoclaving components (for example, washing disassembled equipment such as from the Waukesha Pumps. Assembly of Vispros and FUS Pumps and associated documentation) parts used in aseptic manufacturing operations. Reading and understanding written instruction as detailed on production batch records. Routine aseptic gowning practices. NOTE: Must have flexibility, discipline and not fall out of established limits. Stocking of consumable items, such as bouffant hats and beard covers. Stocking of sterile and non-sterile gowns. etc. | 5/27/2020 |
| 11100 | Akoya Marlborough, MA Scientist, Applications MS in a life science Exp: 1-2 year(s) |
Akoya Biosciences is seeking an experienced immunohistochemist to join our Applications group in Marlborough, MA, which is responsible for developing new multiplexed immunohistochemistry methods and running exploratory and validation studies, using Akoya’s Phenoptics multiplexed immunofluorescence platform. Phenoptics enables staining of up to 9 colors, utilizing OPAL detection reagents and Vectra multispectral imaging instruments, providing unparalleled cell-level and architectural-level tissue analysis capabilities. The Applications group is a dynamic team that engages with important strategic collaborators in academia and in the pharmaceutical industry to help facilitate adoption of the Phenoptics platform and to develop new applications. etc. | 5/27/2020 |
| 11101 | Alcami Wilmington, NC Associate Scientist - Biotech MS in pharmaceutical science, chemistry, or equivalent Exp: None required for MS candidates |
The Associate Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also be required to work on method development/method validation projects. For this position HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. etc. | 5/27/2020 |
| 11102 | Alcami Charleston, SC Manufacturing Tech I - 3rd Shift HS diploma/AS/AA Exp: 0-2 year(s) |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. etc. | 5/27/2020 |
| 11103 | Alcami Charleston, SC Quality Specialist MS in chemistry, biology or related Exp: 1+ year(s) |
The Quality Specialist II is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. etc. | 5/27/2020 |
| 11104 | Alcami St. Louis, MO Quality Specialist II MS in chemistry, biology or related Exp: 1+ year(s) |
The Quality Specialist II is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. etc. | 5/27/2020 |
| 11105 | Alcami Wilmington, NC Quality Specialist II MS in chemistry, biology or related Exp: 1+ year(s) |
The Quality Specialist II is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. etc. | 5/27/2020 |
| 11106 | Alcami Durham, NC Quality Specialist II MS in chemistry, biology or related Exp: 1+ year(s) |
The Quality Specialist II is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. etc. | 5/27/2020 |
| 11107 | Aldevron Fargo, ND Downstream GMP Biomanufacturing Operator AS/BS in a life science Exp: 1+ year(s) |
The Downstream GMP Biomanufacturing Operator works daily within Aldevron’s manufacturing areas, performing tasks associated with Aldevron’s GMP plasmid DNA production services. This role focuses specifically on downstream associated with the purification of plasmid DNA, including lysis, Anion Exchange Chromatography, Hydrophobic Interaction Chromatography (void and enrichment), Thiophilic Absorption Chromatography, diafiltration, and small-scale processing as well as linearization. etc. | 5/27/2020 |
| 11108 | Aldevron Madison, WI Associate Scientist II, Fermentation AS/BS in biology, microbiology, biochemistry or related Exp: 1+ year(s) |
The Associate Scientist II, Fermentation supports the execution of 1-L to 1000-L scale microbial fermentations. This role works collaboratively with team members and as an individual contributor. This position requires excellent laboratory skills, attention to detail and excellent documentation practices. Responsibilities: Assist in execution of 1 L 1000 L scale fermentations. Prepare microbiological culture media and other culture reagents. Transform E. coli with plasmid DNA. Harvest E. coli cultures using centrifuges and TFF devices. Prepare and analyze cell lysates (SDS PAGE, Western Blot, Concentration Assays). etc. | 5/27/2020 |
| 11109 | Aldevron Madison, WI Quality Control Scientist I, Protein BS in chemistry, biochemistry, genetics, cell biology or related Exp: 1 year |
The Quality Control (QC) Scientist I, Protein, supports production of recombinant proteins. This role is primarily responsible for performing release testing and ensuring that products meet or exceed all quality specifications. This role also supports the management and execution of stability studies. Responsibilities: Accurately record experimental results in real-time; store/save and report data per Aldevron conventions. Work with analytical equipment routinely used to characterize recombinant proteins, including Reverse Phase HPLC, Analytical Size Exclusion Chromatography, SDS-PAGE and Western Blot, UV/Vis and Fluorescence Spectroscopy (cuvette and multi-well plate), ELISA, and Endotoxin Detection Assays. Assist in qualification of test methods, writing and review of documents, internal process reviews, and basic equipment maintenance. etc. | 5/27/2020 |
| 11110 | Aldevron Madison, WI Shipping and Receiving Specialist HS diploma or equivalent Exp: 1-2 year(s) |
The Shipping and Receiving Specialist is responsible for supporting the storage and inventory management of materials, the shipping of materials to the clients, and staging materials for client and internal projects. Responsibilities: Responsible for receiving and storing of incoming materials. Performs physical inspection of materials at the time of arrival. Responsible for ensuring purchase orders match items received. Package material for shipment according to established procedures. Performs periodic cycle counts to verify inventory accuracy. etc. | 5/27/2020 |
| 11111 | Aldevron Fargo, ND Material Handler - 2nd Shift HS diploma or equivalent Exp: 1 year |
The Material Handler receives and issues inventory to/from the manufacturing operations. This role is responsible for properly identifying and inventorying material all material and equipment from receiving and production. Responsibilities: Receiving and placing material and equipment into stock from Receiving and Manufacturing. Responsible for the receipt of materials into the Raw Materials Management database. Restock picking locations as needed. Tracking and monitoring inventory levels. Conduct regularly scheduled stock counts. Making sure incoming material is labeled. etc. | 5/27/2020 |
| 11112 | Aldevron Fargo, ND Upstream GMP-Source Biomanufacturing Operator AS/BS in a life science Exp: 1+ year(s) |
The Upstream GMP Biomanufacturing Operator works daily within Aldevron’s manufacturing areas, performing tasks associated with Aldevron’s GMP-Source plasmid DNA production services. This role focuses specifically on bacterial cell growth, including transformation, subculture, cell banking, fermentation, shake flask growth, wave growth, and harvest. Responsibilities: Plan and submit inventory requisitions. Plan and preparation of production events and process plan memos. Coordinate production events with buffer preparation operators. Perform upstream production events. etc. | 5/27/2020 |
| 11113 | Aldevron Madison, WI Associate Scientist II, Biomanufacturing AS/BS in biochemistry. Biotechnology, biology or related Exp: 0-2 year(s) |
The Associate Scientist II, Biomanufacturing role is responsible for duties relating to standard purification of antibodies and proteins. The Associate Scientist II will interact closely with all members of the lab team and will support various lab activities as assigned. Responsibilities: Purify multiple recombinant proteins and/or antibodies using chromatography skid. Using dialysis tube or TFF, perform buffer exchange and final formulation of recombinant protein. Routinely pack, unpack clean, and regenerate resins in chromatography columns for protein purification process. Characterize in-process samples and purified proteins using methods including SDS PAGE, Western Blot, Bradford Assay, and ELISA. etc. | 5/27/2020 |
| 11114 | AliveCor Mountain View, CA Hardware Test Engineer BS in electrical engineering or related Exp: 1-5 year(s) |
AliveCor, the creator of the Kardia Mobile ECG app, seeks a Hardware Test Engineer to join an exciting start-up that is changing the face of mobile health. As the Hardware Test Engineer, you will be a crucial member of hardware R&D team responsible for ensuring that AliveCor products perform as intended and meet/exceed customer expectations. You will work closely with our Quality, Regulatory, Software Engineering, Product Management, and Creative teams to ensure new products perform as intended while fully documenting the verification process. You will also work with our manufacturing team to implement and support manufacturing test fixtures. etc. | 5/27/2020 |
| 11115 | Alkermes Wilmington, OH Process Engineer-OSD BS in a science or engineering Exp: 0-3 years |
Support and assist in the manufacture of pharmaceutical products for commercial and clinical supplies. Where applicable, the candidate may be tasked with scale-up and transfer of formulations/processes to the commercial production facility, designing and recommending equipment purchases, and writing/executing qualification/validation protocols. Troubleshooting of automated equipment for pharmaceutical manufacturing, identification and implementation of process/equipment improvements to reduce waste and increase process reliability, and cleaning process development are also within the scope of this position. Essential Functions: Troubleshoot and maintain manufacturing systems, processes and equipment. Support development of cleaning processes for the manufacturing area. etc. | 5/27/2020 |
| 11116 | Alkermes Wilmington, OH Process Engineer I-Bulk BS in engineering Exp: 1-2 year(s) |
Support and assist in the manufacture of pharmaceutical products for commercial and clinical supplies. Scale-up and transfer formulations/processes to production facility, design and recommend equipment purchases, write and execute qualification/validation protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process/equipment improvements (utilizing Change Control system) to reduce waste and increase process reliability. Support of manufacturing management in periodic review of existing and new revisions to manufacturing documentation in regards to, but not limited to, Operability, Technical accuracy (technical reviews), Compliance, Process Robustness. Perform process and equipment evaluation (FMEA, etc.) to identify risks and weaknesses in new and current processes, etc. | 5/27/2020 |
| 11117 | Alkermes Waltham, MA Contract Senior Research Associate (In vitro) MS Exp: 1-5 year(s) |
We are looking for a highly-collaborative temporary stem cell biologist with strong interpersonal and communication skills. We are developing new disease models to build advanced drug discovery assays in immune oncology and neurobiology. This position requires meticulous cell culture abilities, excellent communication skills, and will work in a cross-functional team environment supporting multiple projects. The successful candidate will have experience culturing multiple cell types, including immortalized cell lines and human stem cells with different media and culture requirements. Many of our cultures are maintained in an antibiotic free media. Ideally, this individual will also assist with RNA and DNA purification and setting up next generation sequencing runs on our Ion Torrent sequencers. etc. | 5/27/2020 |
| 11118 | Alnylam Cambridge, MA Associate Scientist II, Research Analytical, QC and Annealing BS/MS in chemistry, biochemistry, or related Exp: 0-8 years |
The Research Department at Alnylam is seeking a highly motivated Associate Scientist to join our RNA QC and annealing group and support RNAi-based research and drug discovery. The successful candidate will help in the quality control and annealing of oligonucleotides and siRNA’s for research studies. Additionally, they will evaluate new formulation approaches for CNS and ocular delivery applications and develop suitable assays such as the Bacterial Endotoxins Test (BET) for improved quality control. Summary of Key Responsibilities: Preparation of siRNA duplexes and QC of siRNA to support research and drug discovery. Analysis and analytical method development of newly chemically modified oligonucleotides (single strands and siRNA duplexes). etc. | 5/27/2020 |
| 11119 | American Regent Columbus, OH QC Microbiologist I BS in microbiology, biology, or other life science Exp: 1 year |
This position in the Microbiology Laboratory will be primarily responsible for performing the microbiological testing for in-process as well as monitoring of controlled manufacturing facilities and utility systems. essential Duties and Responsibilities: Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Ensure all work is performed and documented in accordance with existing company policies, procedures, and Current Good Manufacturing Practices, health and safety requirements. Plan daily workload to meet requirements. etc. | 5/27/2020 |
| 11120 | American Regent New Albany, OH QA Quality Systems Specialist I BS/BA Exp: 1 year |
The Quality Systems (QS) Specialist I will be responsible for effectively ensuring non-routine events are investigated and documented in accordance with company SOPs, policies and cGMPs. This is a cross-functional position that interacts with All departments at PharmaForce. The incumbent will participate in organizing the quality systems to meet or exceed the company's quality expectations. ESSENTIAL DUTIES AND RESPONSIBILITIES: Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Under the direction of the Quality Systems (QS) Manager, the QS Specialist I will: Coordinate specific departmental activities with the goal of maximizing efficiency of management control systems, programs, policies, work methods and procedures. etc. | 5/27/2020 |
| 11121 | Adverum Biotechnologies Redwood City, CA Assay Development Research Associate I BS Exp: Entry level |
Adverum is looking for a Research Associate to join our team in Redwood City. This position reports to a Scientist and is a technical position for a highly motivated Research Associate to support the Assay Development group in an industry setting. The candidate would particularly be involved in cell culture service. The Responsibilities will also include routine lab maintenance, GxP materials receiving and shipping, writing test procedures. Maintaining good documentation is required. etc. | 5/26/2020 |
| 11122 | Aesculap Irvine, CA PM Inspector (Excel Packing Pooling) HS diploma or equivalent Exp: 1-5 year(s) |
Under general supervision, performs visual in-process inspection for quality and packing of finished Excel products. Responsibilities: Essential Duties: Responsible to ensure compliance of product with the quality requirements. Responsible for verifying the documentation/test report and relevant documents of all tests conducted. Responsible for filing, compilation and documentation of the quality batch records. Responsible to update the results. Provides immediate feedback to production line and immediate leadership on all quality related problems. etc. | 5/26/2020 |
| 11123 | Aesculap Irvine, CA Inspector (Injection Molding ADD/PAB) HS diploma or equivalent Exp: 0-4 years |
Works under the direction of the Supervisor/Lead Processing Technician/Setup Technician. Using specific methods, inspects plastic molded parts for visual dimensional defects; performs light to medium packaging and product handling functions. Completes documents required to release parts. Performs cleanup of equipment and facilities in the Injection Mold production areas. Attends injection molding machine and subassembly equipment. Does minor trouble-shooting not requiring a maintenance mechanic or process technician (i.e. Lead Processing Technician, Setup Technician, Process Technician). etc. | 5/26/2020 |
| 11124 | Agilent Boulder, PA Manufacturing Associate HS diploma or equivalent Exp: 1+ year(s) |
As a Manufacturing Associate, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. Responsible for performing a variety of support duties in one or more manufacturing areas. Duties may be related to cleaning, ordering, stocking, preparing, installing, maintaining, repairing and supporting manufacturing equipment and processes. etc. | 5/26/2020 |
| 11125 | Agilent Wilmington, DE Electronics Technician I unspecified Exp: 1+ year(s) |
The Electronics Technician I position is required to support the manufacture of GCMS instruments. This position will be responsible for testing, troubleshooting, and reworking instruments within the flow of the GCMS production lines. This role involves working with electronic assemblies in support of shipment of instruments and support parts to meet customer needs. This position works closely with R&D development engineers on NPI products and value engineering improvements. etc. | 5/26/2020 |
| 11126 | Agilent Frederick, CO Manufacturing Associate - Entry (2nd Shift) HS diploma Exp: 1-2 year(s) |
As a Manufacturing Associate, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. Responsible for performing a variety of support duties in one or more manufacturing areas. Duties may be related to cleaning, ordering, stocking, preparing, installing, maintaining, repairing and supporting manufacturing equipment and processes. etc. | 5/26/2020 |
| 11127 | AGC Biologics , CO Manufacturing Associate I-IV, Downstream BS in chemistry or biology Exp: 1-8 year(s) |
The Manufacturing Associate I-IV, Downstream performs GMP manufacturing operations safely, reliably and in compliance with stated processes. We offer a dynamic environment, innovation, operational excellence, and career growth. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. Complete required processing documentation including deviation reports, change control, product change over, etc. | 5/26/2020 |
| 11128 | AGC Biologics Bothell, WA Development Associate I (Upstream) Contract AS/BS in a life science or engineering Exp: 0-3 years |
This is a Development Associates position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. PRINCIPAL RESPONSIBILITIES: Maintain lab including cleaning, autoclaving reactors, stocking laboratory supplies and performing maintenance on laboratory equipment. etc. | 5/26/2020 |
| 11129 | AGC Biologics Bothell, WA Manufacturing Associate I-IV, Downstream (Contract) BS in chemistry or biology Exp: 1-8 year(s) |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. Complete required processing documentation including deviation reports, change control, product change over, etc. | 5/26/2020 |
| 11130 | Aesculap Allentown, PA Molding Technician (3rd Shift - Injection Molding) HS diploma or equivalent Exp: 0 - 6 months |
Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organizations products according to specifications and schedules, volume, cost and waste targets, or quality standards. Operates machines and production equipment safely and in accordance with instructions. Monitors the quality of output to identify, discard or remanufacture products. Troubleshoots problems by contributing to team with input, feedback and/or ideas for improvement. etc. | 5/26/2020 |
| 11131 | Aesculap Irvine, CA Sterilization Product Handler HS diploma or equivalent Exp: 6 months |
Responsibilities: Essential Duties: Assists supervisor to ensure that production operators have sufficient stock of materials. Collects, checks and keeps records of materials flow to and from production area. The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor from time to time. etc. | 5/26/2020 |
| 11132 | Aesculap Daytona Beach, FL QC Inspector HS diploma or equivalent Exp: 6 months - 2 years |
Responsibilities: Essential Duties: Performs repetitive and routine inspections, checks, tests and sampling procedures of standard parts, units, equipment or materials. Performs inspections of purchased parts, subassemblies or finished company products according to well defined criteria using standard physical, mechanical and/or electrical measurements. Reworks or rejects subassemblies or finished products as required. Performs audits to ensure standards of quality are maintained. etc. | 5/26/2020 |
| 11133 | Aesculap Daytona Beach, FL Entry Production Technician HS diploma or equivalent Exp: 0-6 months |
The primary responsibility of a Production Technician is to oversee the operation of production equipment for the manufacturing of pharmaceutical products. This work will include loading & unloading of raw materials, verifying proper machine operation, clearing machine jams when they occur, testing and verifying the quality of the product being produced, and reporting all required data during runs. This individual must possess an overall knowledge of GMP’s, ISO, and OSHA requirements in the manufacturing environment. This position shall operate in accordance with company policies & procedures, FDA regulations, and ISO standards. etc. | 5/26/2020 |
| 11134 | Aesculap Irvine, CA Set Up Tech (PIC Blow Molding) HS diploma or equivalent Exp: 1-2 year(s) |
Under the direction of the Supervisor/Lead Processing Technician, set up, operate and perform machine/equipment installations and repairs on plastics equipment to produce quality-molded components. Responsibilities: Essential Duties: Properly set processing equipment and molding tools as instructed by Shift Supervisor, Chief Operator or Scheduler. Set up all operating parameters on above equipment as per process data card (i.e., heaters, times pressures, speeds, type of material and electronic process controllers). Check on the quality of molded products through Process Tech or Quality Inspector or by self-inspection. Variations are communicated with Process Tech or Supervisor to take necessary action. (All Setup Technicians must be able to operate all basic quality control measuring devices.) etc. | 5/26/2020 |
| 11135 | Boston Heart Diagnostics Framingham, MA Specimen Processor HS Diploma/GED Exp: 0-2 years |
The Specimen Processor enters all patient demographic and testing information into the laboratory information system and prepares blood samples for the analytical phase. Accurately and efficiently complete data entry of patient info and order codes into the system. Verify that samples received are: labeled with the correct patient identifiers, the correct sample type, and within stability for the requested test(s) | 5/24/2020 |
| 11136 | Boston Heart Diagnostics Framingham, MA Medical Technologist Some college courses (3 years), training in medical technology Exp: 1-2 years |
Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of test examinations. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens. | 5/24/2020 |
| 11137 | Bristol Myers Squibb New Brunswick, NJ Associate Process Engineer BS/BA in biomedical/mechanical engineering Exp: 0-2 years in pharma/biotech |
The Associate Process Engineer provides technical leadership related to new and existing sterile drug products. This position is supports the technical interface with R&D to ensure design and transfer of robust manufacturing processes for new products and key life cycle management products, development of new technology for optimization and continuous improvement in manufacturing operations, providing specialized expertise as necessary to complement site capabilities for critical investigations or process improvements, setting relevant standards and creating and maintaining associated Directives (e.g, for tech transfer, Product monitoring, etc). | 5/24/2020 |
| 11138 | Bristol Myers Squibb Syracuse, NY Assistant Scientist - Night Shift BS in sciences Exp: 0-3 years |
Duties include conducting routine and non-routine testing of materials and products using a variety of equipment and test methods upon demonstrating the ability to perform and understand required methods. Each analyst is responsible for capturing data accurately and timely followed by promptly entering testing results within the appropriate data collection system (e.g., LIMS, LES, etc). | 5/24/2020 |
| 11139 | Bristol Myers Squibb Warren, NJ Associate Bioengineer II – Cell Culture Engineering BS or MS in biological sciences/engineering Exp: 0-1 years in industry |
With minimal supervision, design and execute experiments to assess impact of cellular metabolism and cytokine signaling on T cell phenotype Optimize cell culture conditions as well as media components that can help improve process performance and achieve desired product attributes Critically analyze and interpret data using statistical methods Summarize experimental results and present them for internal discussions. | 5/24/2020 |
| 11140 | Brooks South Plainfield, NJ Associate Customer Support Scientist I BS/BA in biological sciences Exp: Entry Level |
The specific focus is on the Gene Synthesis and Cloning/Mutagenesis services. They advocate the client’s perspective to ensure excellent customer service. They enjoy interacting with people daily via phone, email or live chat. They work within our systems to identify the cause of an issue and can effectively address questions or concerns. When customers have ambiguous questions, they can provide meaningful responses. | 5/24/2020 |
| 11141 | Brooks South Plainfield, NJ Product Marketing Associate BS/BA in business, marketing or life sciences Exp: 1-2 years in biotech/life sciences |
Gather and review product market trends and competitive landscape to identify target markets and develop lead generation strategies. Support generating opportunities through new services or service differentiation by representing the voice of the customer. Create and maintain competitive matrix and fine-tune service offerings and forecasts accordingly | 5/24/2020 |
| 11142 | Brooks South Plainfield, NJ Associate Customer Support Scientist BS/BA in life sciences or business admin Exp: Entry Level |
The Associate Scientist I, Project Management position in Molecular Genetics is a non-bench role that works closely with customers and the lab in order to effectively manage the customer interaction with GENEWIZ. Provide consultation and troubleshooting for the molecular biology services including: PCR and sequencing applications, DNA, RNA, cDNA applications, Gene synthesis | 5/24/2020 |
| 11143 | Brooks South Plainfield, NJ Associate Scientist I BS/BA in biological sciences Exp: 1+ years in lab |
Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. Communicate with customers by phone and e-mail in a friendly and professional manner | 5/24/2020 |
| 11144 | Brunswick Lab Sossuthborough, MA Laboratory Assistant – HPLC and Platereader-based Assays BS or MS in chemistry Exp: 1-2 years in assay development |
Highly independent, hands-on HPLC and 96-well platereader based assays with limited guidance after training. Experience with HPLC or GC strongly preferred. Process HPLC and bioanalytical assays using 96-well or other multi-well microplate reader. Must be well-organized; Must have high attention to details and precise technical skills to process large number of samples | 5/24/2020 |
| 11145 | BD Baltimiore, MD Quality Document Management Specialist I BS/BA Exp: No experience Necessary |
This position supports the Release Control function for the Prepared Media plant. The position requires the timely entry of various forms of data to meet production and quality goals. Requires review of records and data for completeness and GMP compliance. Associate will perform final release of products. Metrics tracking and reporting may be required. | 5/24/2020 |
| 11146 | BD Baltimiore, MD Scientist I BS/BA in life sciences/engineering Exp: 1-4 years in lab work |
This person will be responsible for assisting in the design, development, integration and qualification of assays and/or specimen processing workflows on automateddiagnosticssystems.The successful candidate may also be expected to provide support in execution of clinical studies to validate performance of the assays andassemble relevant information in support of regulatory submissions. | 5/24/2020 |
| 11147 | BD San Jose, CA Supplier Quality Engineer BS/BA in related field Exp: No experience Necessary |
The Quality Engineer is primarily responsible for reviewing and assessing Quality Notifications, Complaints, Deviation/Waivers and other cGMP activities for the assigned product lines in the instrument plant. The QM Engineer I oversees QC operations within the instrument plant and assuring documentation and procedures are followed, updated and maintained as required by internal Quality Policies and related FDA/GMP guidelines. The QM Engineer I conducts complaint investigations, assists in the investigation of manufacturing issues and provides data and input on technical issues and projects. | 5/24/2020 |
| 11148 | BD Cayey, PR Quality Technician BS/BA in life/medical sciences Exp: 1-3 years in lab |
The Quality Control (QC) Technician is responsible for performing QC final testing of products, as well as, conducting raw material, stability, complaint, and special investigation testing. Is also responsible for ensuring all testing are performed correctly and results are reported promptly. Perform testing for Bactec product line. Report results on data forms. Perform physical, chemical and microbiological testing to raw materials, finished products and the record results. | 5/24/2020 |
| 11149 | BD Sandy, UT Quality Control Inspector HS Diploma/GED Exp: 1 year in mechanical inspection |
The Quality Control Inspector will measure key quality characteristics on various molded plastic components and mold steel components. Enter data into computer for analysis and prepare graphs and charts for data analysis. Assist engineering in product design verification, process qualifications, and validations. Measure key quality characteristics on various molded plastic components and mold steel components. | 5/24/2020 |
| 11150 | Cambrex Charles City, IA Process Engineer BS in chemical engineering Exp: 1-3 years in manufacturing environment |
The Process Engineer will be responsible for implementation of projects for the manufacture of APIs and bulk intermediates and other products from development through piloting and/or commercial production. Writing batch records, cleaning records, SOPs, campaign reports, supplements, and investigation/deviation reports as needed to support production operations. | 5/24/2020 |
| 11151 | Cambrex Longmont, CO Drug Process Engineer BS/BA Exp: 0-2 years |
The position will be responsible for coordinating projects through the Drug Product manufacturing area working with multiple departments to ensure projects are executed on time. Responsible for the conducting demonstration/notebook batch production and creation of cGMP manufacturing batch records to introduce early phase drug product into the 2600 Drug Product Facility. The ideal candidate will have experience in the formulation, optimization and scale-up of solid dose drug product. | 5/24/2020 |
| 11152 | BioAgilytix Durham, NC Analyst BS/BA in life sciences Exp: 1 year in lab |
Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export). Prepare summary tables. Participate in assay development and validation | 5/24/2020 |
| 11153 | Thermo Fisher Scientific Cambridge, MA Cell Culture Lab Support BS/BA in related field Exp: 1-3 years |
Follows well defined procedures and safety requirements as outlined by Best Practices, SOP’s & work instructions. Take direction from Site Supervisor/Manager (and Team Lead) regarding daily duties. Makes decisions and utilizes available resources to meet customer requirements, independently. Analyzes/maintains/reconciles various customer and Thermo Fisher reports to ensure customer and Thermo Fisher requirements are met. | 5/24/2020 |
| 11154 | Cambrex Malborough, MA Cleanroom Technician HS Diploma/GED Exp: 0-2 years, drivers license |
A Cleanroom Services Technician will support the Cleanroom Services team by assisting filed analysts with a wide range of tasks including: equipment setup and stocking supplies, vehicle and equipment maintenance, facility administrative housekeeping. Additionally, this role will be responsible performing work at client sites as needed. | 5/24/2020 |
| 11155 | Biorasi Aventura, FL Business Development Associate BS/BA in life sciences or business admin Exp: 0-2 years |
Responsible for identifying new potential client opportunities and lead generation through market research, client inquires and other methods to client development. Actively pursue qualified leads and nurture relationships and opportunities. Organize, coordinate and attend client facing and internal meetings to develop contact relationships and Solution development. | 5/23/2020 |
| 11156 | Biorasi Aventura, FL Associate, Program Development BS/BA in life sciences or business admin Exp: 0-2 years |
Responsible for identifying new potential client opportunities and lead generation through market research, client inquires and other methods to client development. Actively pursue qualified leads and nurture relationships and opportunities. Organize, coordinate and attend client facing and internal meetings to develop contact relationships and Solution development. | 5/23/2020 |
| 11157 | BiorReference Laboratories Elmwood Park, NJ Medical Lab Technician AS in medical/chemical/biological sciences Exp: 1 year work experience |
Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. Maintains an up to date working knowledge of all technical procedures in the department and operations of all instrumentation. Reviews all pertinent SOPMs. Manipulate and operate simple and complex laboratory equipment including computers; may perform maintenance and limited tear down and replacement of parts of laboratory equipment; problem-solve equipment malfunctions. | 5/23/2020 |
| 11158 | BiorReference Laboratories Baltimore, MD Phlebotomist Phlebotomy certification Exp: 6 months work experience |
The Phlebotomist provides expertise in blood draws and specimen preparation. Their ability to put patients at ease and obtain sufficient samples with minimal discomfort to patients across a wide demographic is critical to our commitment to high quality care for our patients and those of our partners. Experience doing blood draws, labeling specimens, centrifuging specimens, recording maintenance data and decontamination, updating patient information, etc. | 5/23/2020 |
| 11159 | BiorReference Laboratories Elmwood Park, NJ Medical Lab Technician AS in medical/chemical/biological sciences Exp: 1 year work experience |
Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. Maintains an up to date working knowledge of all technical procedures in the department and operations of all instrumentation. Reviews all pertinent SOPMs. Manipulate and operate simple and complex laboratory equipment including computers; may perform maintenance and limited tear down and replacement of parts of laboratory equipment; problem-solve equipment malfunctions. | 5/23/2020 |
| 11160 | BiorReference Laboratories Melbourne, FL Specimen Processor HS Diploma/GED Exp: 0-2 years |
The Specimen Processor must maintain departmental production goals to ensure hourly specimen flow to the labs are consistent. In this role, you will prepare samples for shipping, ensuring they are secure and shipped to the correct laboratory. It will also be your responsibility to handle patient medical records with complete accuracy and confidentiality. | 5/23/2020 |
| 11161 | LGC Petaluma, CA Lab Assistant I HS Diploma/GED Exp: 0-2 years |
The Lab Assistant I will perform tasks in support of the Chemical Production department in a high throughput, time sensitive manufacturing environment. Perform assigned tasks using the established protocols and methods on the appropriate equipment and within the given final specifications and timeline. Effectively communicate and coordinate with Chemical Production team members, affected employees in other departments, and the Production Support Supervisor to assure the most efficient use of time and resources. | 5/23/2020 |
| 11162 | LGC Petaluma, CA Oligonucleotide Production Technician I BS/BA in life science or chemistry Exp: 0-2 years |
The Oligo Production Technician I is responsible for performing day to day production activities in the custom oligonucleotide (oligo) production lab. Production activities will be performed in a timely fashion and in compliance with company procedures. Performs all assigned job functions per documented procedures or as directed by the supervisor/manager. Perform oligonucleotide synthesis/purification according to established procedures. | 5/23/2020 |
| 11163 | LGC Petaluma, CA Oligonucleotide Production Technician I (9282) BS/BA in life science or chemistry Exp: 0-2 years |
The Oligo Production Technician I is responsible for performing day to day production activities in the custom oligonucleotide (oligo) production lab. Production activities will be performed in a timely fashion and in compliance with company procedures. Performs all assigned job functions per documented procedures or as directed by the supervisor/manager. Perform oligonucleotide synthesis/purification according to established procedures. | 5/23/2020 |
| 11164 | Biosero West Coast, na Field Applications Scientist MS in life sciences, biochem, or related Exp: 1-3 years experience |
The Field Application Scientist will work closely within a matrix environment including Sales, Integration and Engineering, Support, and Marketing to provide the best-integrated solutions to our customers. Responsibilities include working directly with customers to assist in the design of integrated robotic systems, provide on-site support, and assist in sales demonstrations and proposal submission to customers. | 5/23/2020 |
| 11165 | Bio-Techne San Jose, CA Manufacturing Technician (Compounding) AS or BS/BA in chemical/biological sciences or engineering Exp: 0-3 years |
The successful applicant will work with other members of the consumable production team as well as a multidisciplinary team of engineers and scientists to support routine production activities for reagent formulation/ compounding team. Help maintain and track supplies inventory. Preparation of buffers and other biochemical formulations . Conjugation of protein solutions | 5/23/2020 |
| 11166 | Bio-Techne San Jose, CA Manufacturing Technician ( Swing Shift, Wes Cartridge ) AA degree Exp: 1+ years of lab/manufacturing experience |
Operate and maintain robotic and manufacturing equipment. Ability to use hand tools such as small wrenches, pliers, tweezers, etc. Perform in-process QC and record results. Document production batch records/travelers and computer data entry. Maintain and track raw material inventory | 5/23/2020 |
| 11167 | Bio-Techne Minneapolis, MN Research Associate, Cell Culture and Stem Cell Media Operations and Support Services BS/BA in biological sciences Exp: 0-2 years in lab |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Tuesday through Saturday workweek. | 5/23/2020 |
| 11168 | Bio-Techne Minneapolis, MN Advanced Research Associate, Conjugation MS in biological sciences Exp: 0-2 years |
This position is responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel.Prepares conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research according to written and non written procedures. | 5/23/2020 |
| 11169 | Bio-Techne Minneapolis, MN Manufacturing Technician HS Diploma/GED Exp: 0-2 years |
The responsibilities of the Manufacturing Technician are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include filling containers with product, feeding a production machine, labeling product, recording data, operating equipment, formulation, and plate coating. | 5/23/2020 |
| 11170 | Bio-Techne Minneapolis, MN Equipment Technician I HS Diploma/GED Exp: 1-3 years, 1 year with Associate's degree |
As an Equipment Technician I, you will perform preventative maintenance and repair malfunctioning new and existing minor equipment. In doing so, you will manage and document your work orders, respond to supervisory alarms during business hours, and complete routine inspections on equipment. Perform and document scheduled preventative maintenance on minor equipment. Perform minor repairs to malfunctioning equipment per work orders | 5/23/2020 |
| 11171 | Bio-Techne Minneapolis, MN Research Associate, Cell Culture and Stem Cell Media Operations BS/BA in biological sciences Exp: 0-2 years in lab |
The main responsibility of this position it to maintain production of mouse embryonic fibroblasts. Additional responsibilities include media and supplement production, QC testing of methylcellulose-containing cell culture media, and cell culture of multiple cell lines. Perform additional duties as assigned. Preferred skills include cell culture, high attention to detail, strong communication and organizational skills. | 5/23/2020 |
| 11172 | BioTelemetry Rochester, NY Test Engineer (Contract to hire) BS in engineering, computer/information sciences Exp: 1-3 years as software test engineer |
The Test Engineer I will provide technical testing expertise as part of an Agile development team and be a trusted team member for BioTel Research’s clinical research services. The Test Engineer will refine the product backlog, ensuring the quality and reliability of all functional components used. They will ensure that all systems meet customer requirements in a manner that is consistent with applicable regulatory requirements especially with regard to validation processes outlined in Good Clinical Practice and Good Manufacturing Practice and maintaining Separation of Duties. | 5/23/2020 |
| 11173 | BioTel Heart Linwood, PA Distribution Quality Technician HS Diploma/GED Exp: 1 year in QA |
Processing new devices, failed devices and performing QA audits as required. Inspection of incoming goods. Inspection of finished products for final release. Responsible for performing analysis and documentation of all pending failures from out of box, check-in and field failures and generating summary reports at the service center locations. Provide device training when requested. | 5/23/2020 |
| 11174 | Biotherapeutics Blacksburg, VA Animal Technician BS or MS Exp: 1 year |
Work independently and collaboratively in a matrixed environment. Assume the role of animal facility manager. Maintain housing and husbandry, genotyping, regulatory and safety, and keep thorough record for animals. Develop breeding and genotyping protocols new strains of mice | 5/23/2020 |
| 11175 | Biotherapeutics Blacksburg, VA Chemistry Technician BS/BA in chemistry Exp: 1 year |
Chemistry Work: Set up a recrystallization pipeline at BioTherapeutics for abscisic acid (ABA) and punicic acid (PUA), with the intention of recrystallizing additional compounds. Conduct recrystallization optimization analytics. Interface with chemistry department with the ABA and PUA development. Setup chemistry work space and keep detailed records of all activities, record these activities in ASANA, the Google Drive, and in a laboratory notebook. Provide weekly and bi-weekly updates of chemistry progress to the BioTherapeutics team. Working with a food science expert to find ways to emulsify pomegranate seed oil for beverage applications. | 5/23/2020 |
| 11176 | Biotherapeutics Blacksburg, VA Translational Medicine Researcher BS or MS Exp: 1 year in lab |
Work independently and collaboratively in a matrixed environment. Assume the role of project manager and generate supportive data for pre-clinical experiments. Assay optimization to characterize immunity at the molecular, cellular and tissue levels. Maintain and stock materials/reagents/products used in laboratory procedures | 5/23/2020 |
| 11177 | Biotronik na, ND Sales Representative: North Dakota MS in life sciences or business Exp: 1 years as clinical specialist |
In this role you will gain market share in the cardiac rhythm business by promoting, selling, and servicing Biotronik’s products within an assigned territory. Sales Representatives perform field promotional work to sell and develop new business; this may include work with current accounts, or with customers where product acceptance has not been established. Biotronik seeks candidates who will meet and exceed our customer expectations by striving for the greatest possible reliability and quality in our products, processes and systems by being accountable and taking action. | 5/23/2020 |
| 11178 | Biotronik Los Angeles, CA Vascular Intervention Sales Representative MS in life sciences or business Exp: 1 year in medical industry sales |
Conduct sales calls to promote, sell, and service BIOTRONIK products and services to existing and competitive customers. Assists in the utilization of BIOTRONIK products by supporting implant procedures in the Cardiac Catheterization Laboratory. Develop and implement quarterly sales plan to achieve sales goals and objectives. Maintain exceptional knowledge of BIOTRONIK products, changes in the clinical landscape, and of competitors’ product offering | 5/23/2020 |
| 11179 | BMG Labtech Boston, MA Technical Service Representative BS/BA in biological sciences Exp: 1-3 years in lab |
BMG LABTECH, a market leader in microplate instrumentation, is looking for a motivated individual to join our technical service and support team to be based in the greater Boston, MA area. Provide technical support for BMG LABTECH instrumentation. Inside and outside sales of product service plans, accessories, and upgrades via phone, email, and onsite visits | 5/23/2020 |
| 11180 | Boehringer Ingelheim Ridgefield, CT Laboratory Technician Associates in biological sciences Exp: 0-2 years in animal health/veterinary |
The basic purpose is to conduct technical activities on preclinical toxicity studies according to study protocols. Receives daily tasking assignments, under moderate supervision, from higher level technical personnel having responsibility for coordinating the tasks of a group. Accountable to supervisor for performance and management for scientific elements of a project. | 5/23/2020 |
| 11181 | Boston Analytical Salem, NH Microbiologist BS/BA in biological sciences Exp: 0-2 years |
The QC Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity). | 5/23/2020 |
| 11182 | Boston Analytical Boston, MA Analytical Chemist BS in chemistry or related Exp: 0-5 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 5/23/2020 |
| 11183 | BioVision San Francisco, CA Sales Representative BS or MS in biochemistry or biological sciences Exp: 1-2 years in life science industry |
Meet or exceed sales objectives set by the BioVision management. Learn and master BioVision's product offering and manufacturing capabilities . Establish long-term relationships with the customers and match BioVision's capabilities with customer needs. Identify key contacts and decision makers to maximize the benefits from customer visits | 5/23/2020 |
| 11184 | BMG Labtech Boston, MA Life Science Capital Equipment Sales Associate BS or MS in life sciences Exp: 0-2 years |
We are hiring for a Sales Associate position located in the Boston area. This is a home-office based position providing sales, sales-support, service, training and applications support tasks related to operations in the Northeastern U.S. Use your love of science and lab experience to engage with customers in a variety of research labs. Train users in operation and troubleshoot scientific questions | 5/23/2020 |
| 11185 | Acumed Memphis, TN Sales Associate, Memphis, Tennessee - Future Opportunities BS/BA in a business or medical discipline Exp: 0-3 year(s) |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 5/20/2020 |
| 11186 | Acumed Philadelphia, PA Sales Associate, Philadelphia, Pennsylvania - Future Opportunities BS/BA in a business or medical discipline Exp: 0-3 year(s) |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 5/20/2020 |
| 11187 | Emergent Biosolutions Rockville, MD Facilities Technician BS in engineering or related Exp: Not necessary for BS candidates |
The Associate Metrology Specialist applies knowledge of measurement science, mathematics, physics and electronics to calibrate instrumentation associated with plant and process equipment, ensuring accuracy of pressure, temperature, time, dimensional and other measurements. The metrologist will adapt equipment, standards and procedures to accomplish unique measurements. They will use electronic and hard copy systems to maintain detailed records of calibrations and conduct metrology-related administration. etc. | 5/20/2020 |
| 11188 | Emergent Biosolutions Canton, MA Validation Engineer BS in engineering, biology, or related Exp: 1-3 year(s) |
The Validation Engineer authors, reviews, executes validation documents and activities with cross-functional teams including performing commissioning and qualification activities, temperature mapping, sterilization validation and creating traceability matrixes. The position requires entry level experience in validation using the Kaye Validator equipment, and basic knowledge of validation concepts and industry standards. The Validation Engineer will also be responsible for providing tactical support to ongoing validation activities at the Canton site. etc. | 5/20/2020 |
| 11189 | Emergent Biosolutions Winnipeg, MB Facilities Production Technician HS diploma or equivalent Exp: Not necessary |
Support the manufacturing of pharmaceutical products according to the production schedule. DUTIES & RESPONSIBILITIES: Clean and sanitize equipment as required. Clean the manufacturing and filling areas when required. Perform water sampling and EM sampling. Maintain the inventory of consumables in the cleanrooms. Follow all written procedures according to GMP standards. etc. | 5/20/2020 |
| 11190 | Emergent Biosolutions Baltimore, MD Lead Manufacturing Associate HS diploma/BS in a biological science or biotechnology Exp: 1+ year(s) |
The Manufacturing Associate II position reports to Manager Manufacturing at Emergent Manufacturing Operations Baltimore (EMOB). Prior experience in GMP manufacturing and operation of GMP process equipment are prerequisites. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Operates manufacturing equipment such as: incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in process testing equipment. etc. | 5/20/2020 |
| 11191 | Emergent Biosolutions Baltimore, MD Manufacturing Associate HS diploma/BS in a biological science or biotechnology Exp: 1+ year(s) |
The Manufacturing Associate II position reports to Manager Manufacturing at Emergent Manufacturing Operations Baltimore (EMOB). Prior experience in GMP manufacturing and operation of GMP process equipment are prerequisites. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Operates manufacturing equipment such as: incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in process testing equipment. Demonstrates, understands and adheres to Emergent policies, GMP standards and safety procedures. etc. | 5/20/2020 |
| 11192 | Emergent Biosolutions Baltimore, MD Assistant Technician, Inspection&Packaging HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. Demonstrate competency on assigned qualification blocks: Job specific Standard Operating Procedures. New Inspector Qualification. Execute and document procedural steps in compliance with cGMP standards. Adhere to the procedures and safe practices for movement of product and materials and accurately complete all applicable documentation. This applies to room temperature and cold storage locations. etc. | 5/20/2020 |
| 11193 | Emergent Biosolutions Baltimore, MD Lead Manufacturing Associate BS/BA Exp: Not necessary for BS/BA candidates |
Responsible for the manufacture of biopharmaceuticals, including bench top, scale up and pilot formulations; preparing and operating process equipment, handling materials, dispensing chemicals and interfacing with Maintenance, QA, QC and Tech Group in a cGMP environment. Responsibilities: Work under general supervision of Production Supervisor to manufacture parenteral drugs. Perform compounding of pharmaceutical products following Production Batch Record. Performs and documents developmental formulation batches as required. etc. | 5/20/2020 |
| 11194 | Adaptimmune Philadelphia, PA Quality Assurance Associate- CMC (Deviations & CAPA) BS/BA Exp: 1-2 year(s) |
This Quality Assurance Associate (Deviations & CAPA) role is for an individual, with entry to intermediate level experience in QA discipline, who will be responsible for the initiation, investigation of process deviations aimed at identification of root cause, and implementation of correct actions to prevent recurrence. This role is expected to work in a Good Manufacturing Practices (cGMP) environment, have some level of working knowledge of manufacturing processes, a professional and expert technical writing capability, be action oriented, and be compliant minded while performing and reviewing investigations and CAPA. This position reports directly to the QA Manager with dotted line reporting to QA Senior Specialist. etc. | 5/20/2020 |
| 11195 | Adaptimmune Philadelphia, PA Quality Control Associate Unspecified Exp: 1-3 year(s) |
The Quality Control Associate will be responsible for conducting in-process and finished product testing associated with Adaptimmune clinical trial material. Key Responsibilities: In-process, finished product and stability testing of clinical trial material. Daily maintenance of quality control equipment. Maintenance of Quality Control Protocols, SOP’s and Test Methods. etc. | 5/20/2020 |
| 11196 | Adaptive Biotechnologies South San Francisco, CA Research Associate I/II MS in molecular biology, genetics, bioengineering, or related Exp: Not necessary for MS candidates |
Adaptive Biotechnologies is currently recruiting a Research Associate/Senior Research Associate to join our TCR Discovery team. The successful candidate will work as a part of a team using cellular assays to screen, characterize and develop T cell receptors as potential therapeutic agents. Responsibilities: Isolate and culture human primary immune cells and cell lines. Transfect mammalian cells, as well as optimize and troubleshoot transfection protocols. Use flow cytometric assays to characterize the specificity and potency of T cell receptors, and assess their potential utility as anti-tumor (or alternative disease) therapies. etc. | 5/20/2020 |
| 11197 | Adaptive Biotechnologies Seattle, WA Material Handler BS in a STEM subject Exp: Entry level |
Adaptive Biotechnologies is looking for an outstanding employee to join its Supply Chain team. Responsible for managing the receipt, storage, and distribution of laboratory components and business supplies, Material Handlers at Adaptive perform the key function of keeping our operations running. More than a run-of-the-mill warehouse associate, successful candidates will need to demonstrate meticulous attention to detail and strict adherence to standard operating procedures. The position will work directly with the Procurement, Production, and Finance departments to accurately track, record, and maintain the right amount of raw materials and supplies where they’re needed. etc. | 5/20/2020 |
| 11198 | Adimab Lebanon, NH Research Associate - Antibody Engineering BS in molecular biology, chemical engineering, or biochemistry Exp: Entry level |
We are seeking an aspiring protein engineer to join our Antibody Discovery team. The Research Associate will work in a small team setting to support our integrated antibody discovery and engineering platform. Responsibilities: Manage and conduct antibody selections. Collect, organize, and analyze antibody characterization data. Construct antibody libraries and perform selections. etc. | 5/20/2020 |
| 11199 | Adimab Lebanon, NH Research Associate - Protein Purification BS/MS in biology, chemistry, chemical engineering or related Exp: 1+ year(s) |
We are seeking a Research Associate with experience in protein purification to join our team. This role will support Adimab's novel antibody discovery, maturation, and production platform and closely interface with the Antibody Engineering, Protein Analytics, Molecular Core, and Mammalian Protein Production teams. Responsibilities: Conduct primary purifications of proteins expressed in HEK and CHO cells at various scales (24-well plates to large shake flasks) using automated liquid handlers. Perform secondary purifications of antibodies and antigens using standard chromatography systems at a preparative scale. Formulation of buffers associated with purification methods and resin regeneration. etc. | 5/20/2020 |
| 11200 | Adma Biologics Boca Raton, FL QA Specialist II - Quality, Engineering, Validation BS/BA Exp: 1-5 year(s) |
The QA Specialist II-Quality, Engineering, Validation will Perform a wide variety of Quality Assurance activities to ensure compliance with related regulatory requirements. Primarily responsible for the efficacy and compliance of the change control management system, validation and qualification systems, Corrective and Preventive Action reports (CAPA) and Risk Management policies and procedures. etc. | 5/20/2020 |
| 11201 | Adma Biologics Boca Raton, FL Specialist I QA- Product Release BS/BA in a life or natural science Exp: 1-2 year(s) |
The Specialist I-Quality Assurance-Product Release will Performs a wide variety of Quality Assurance activities to ensure compliance with related regulatory requirements. Main focus on review of batch records and associated documents for product release. Responsibilities: Perform review and support release of manufacturing batch records (in-house and CMO batches) along with all manufacturing supporting documents including but not limited to logs, charts, specifications, and environmental and WFI data. Perform review and release of all Plasma pools, both for internal use and shipment to customers as required. etc. | 5/20/2020 |
| 11202 | Adma Biologics Boca Raton, FL QC Lab Support Associate l BS in biology, chemistry, medical technology, or related Exp: 1-3 year(s) |
The QC Lab Support Associate I will Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. Performs all work under GMP conditions. Provide customer support to QC analysts. etc. | 5/20/2020 |
| 11203 | Adma Biologics Boca Raton, FL Specialist Supply Chain Plasma Operations BS in a life science Exp: Entry Level |
The Plasma Operations Supply Chain Specialist will support all Plasma Operation activities, from plasma shipments from approved donation centers to off-site warehousing through to the Boca manufacturing facility. They will also support plasma lookback process for all plasma programs and the Donor Management process, including sample testing in support of RI-002, Nabi-HB and client programs. Assist with vendor relationships with off-site testing labs and off-site plasma warehouse. Document physical supply chain processes, such as plasma shipments, lookbacks and plasma inventory reconciliation. etc. | 5/20/2020 |
| 11204 | Adma Biologics Boca Raton, FL Specialist I - Supplier Quality Assurance BS/BA Exp: 1-3 year(s) |
The Specialist I-Supplier QA will perform a wide variety of Quality Assurance activities to ensure compliance with regulatory requirements. Responsibilities: Assists with internal audits of all departments at the ADMA facility that are directly involved with activities described in the cGMPs cGMPs or have an impact on activities described in the cGMPs. Support in managing, receiving and coordinating the vendor notifications process. Assists with the coordination and preparation of the Quality Systems Review Board (QSRB) process. etc. | 5/20/2020 |
| 11205 | Adma Biologics Boca Raton, FL Materials Technician I HS diploma or equivalent Exp: <1 year |
We currently have an opportunity available for a Materials Technician centrally located in Boca Raton, FL! Responsibilities: Receive, store and distribute raw materials, intermediate and marketed products in compliance with GMP and company standards. Maintain and order inventory of supplies. Will be working in a cold room environment. etc. | 5/20/2020 |
| 11206 | Adma Biologics Boca Raton, FL Facilities Building Maintenance Technician HS diploma or equivalent Exp: 1 year in a pharmaceutical environment |
We currently have an exciting opportunity available for a Facilities Building Maintenance Technician! Responsibilities: This position ensures the proper maintenance and layout changes of all property, buildings, offices, labs and manufacturing areas; takes corrective action and repairs walls, floors, ceilings, exterior buildings, parking lots and landscape as necessary; provides appropriate notification and documentation of all work performed. General maintenance and repairs within a GMP manufacturing facility. etc. | 5/20/2020 |
| 11207 | Admera Health South Plainfield, NJ Associate Scientist I/II BS/MS in a biological science Exp: 1-3 year(s) |
Responsibilities: Preparing solutions and reagents for performing assays on the bench. Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): RNAseq, Whole Genome Sequencing, Whole Exome Sequencing. Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. etc. | 5/20/2020 |
| 11208 | ABL Rockville, MD Laboratory Research specialist- Immunology BS/MS in immunology or related Exp: 0-2 years |
This position will provide extensive technical support for fulfilling contract requirements for immunological assays. The incumbent will assist with the performance of immune assay conducted in the Immunology laboratory. Assist in the development and qualification of new immunological assays including; but not limited to, the following: Blood and mucosal sample processing, Multicolor-Flow Cytometry based assays, cytokines and other soluble biomarkers Multiplexing assays (Luminex, MSD platforms), ELISA, ELISpot, and Neutralization Assays, among others. Responsible for the isolation of serum, plasma and PBMCs from human and animal blood or mucosal samples. etc. | 5/20/2020 |
| 11209 | Biotechne Wallingford, CT Quality Assurance Specialist BS/BA Exp: 0-2 years |
The Quality Assurance Specialist role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products root cause investigations, document control, internal audits, and other common QMS tasks. Understand and follow appropriate quality protocols: Quality Manual. Record Keeping Guidelines. etc. | 5/20/2020 |
| 11210 | Biotechne San Jose, CA Manufacturing Technician (Finishing) HS diploma/AS in biotechnology, biology, chemistry or related Exp: 1+ year(s) |
Bio-Techne’s Protein Platform Division is looking for a Manufacturing Technician with a motivation to participate in the growth of a fast-paced company engaged in cutting edge biological research. The successful candidate will work with other members of the Reagent production team to make great products, performing tasks involving plate filling, labeling, vialing, and finishing materials. Operation of semi-automated liquid dispensing equipment is integral to the job. etc. | 5/20/2020 |
| 11211 | Biotechne San Jose, CA Manufacturing Technician (Compounding) AS/BS in biotechnology, chemistry, biology, or engineering Exp: 0-3 year(s) |
The successful applicant will work with other members of the consumable production team as well as a multidisciplinary team of engineers and scientists to support routine production activities for reagent formulation/ compounding team. Key Responsibilities: Help maintain and track supplies inventory. Preparation of buffers and other biochemical formulations. Conjugation of protein solutions. Record manufacturing tasks in batch records/traveler. etc. | 5/20/2020 |
| 11212 | Biotechne San Jose, CA Manufacturing Technician ( Swing Shift, Wes Cartridge ) AA/AS Exp: 1+ year(s) |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Key Responsibilities: Operate and maintain robotic and manufacturing equipment. Ability to use hand tools such as small wrenches, pliers, tweezers, etc. Perform in-process QC and record results. Document production batch records/travelers and computer data entry. etc. | 5/20/2020 |
| 11213 | Biotechne Minneapolis, MN Manufacturing Technician HS diploma Exp: 0-2 years |
The responsibilities of a Manufacturing Technician are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. This opportunity is second shift with hours from 1:30 PM to 10:00 PM (Monday - Friday). Key Responsibilities: Set up and build product of low complexity. Load machines and move products. Accurately label vials. etc. | 5/20/2020 |
| 11214 | Biotechne Minneapolis, MN Production Assistant HS diploma or equivalent Exp: 0-2 years |
The responsibilities of the Production Assistant are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include filling containers with product, feeding a production machine, labeling product, recording data, operating equipment, formulation, and plate coating. This position offers 1st shift hours of 5:00am-1:30pm. Key Responsibilities: Operate a production machine to fill containers with product. Feed plates into the machines. Batch and label product. etc. | 5/20/2020 |
| 11215 | 3M Quapaw, OK Advanced Analytical Chemist BS in a scientific or engineering discipline Exp: 1 year |
Primary Responsibilities include but are not limited to the following: Conducting raw material, in process and final product testing in GMP Analytical labs. Analyzing and interpreting results of technical work and testing. Writing, reviewing and approving test results and reports. Crossover and transfer of methods. Conducting Out of Specification investigations. Generating protocols, summary reports, Standard Operating Procedures (SOPs) and other lab-related documents. etc., | 5/19/2020 |
| 11216 | Abcam Branford, CT Research Associate (12 months contract) BS/MS in molecular biology, cell biology, or related Exp: 1-3 year(s) |
The successful candidate will play a hands-on role in the company’s use of a variety of molecular biology, assay development, and protein purification techniques in support of various commercial and academic customer projects to deliver high-quality and on-time customized recombinant antibodies. He or she will partner closely with other team members within the group and be required to make observations, analyze data, and interpret results with supervision. etc. | 5/19/2020 |
| 11217 | Abcam Cambridge, MA Research Associate BS/MS in chemistry, biochemistry, chemical engineering, or related Exp: 1+ year(s) |
We are seeking a Research Associate for a technology development opportunity at Abcam, a leading life science company, in our Cambridge, US office. This position will work within an exciting multi-disciplinary team of scientists and engineers to develop new research tools for use by life scientists worldwide. The Research Associate will be responsible for developing multiplex immunoassays utilizing the FirePlex particle technology. The candidate will support the production and quality control of the FirePlex immunoassay kits. The ideal candidate will be an experienced research scientist that performs well-designed experiments and has a passion for developing technologies to enhance life science research. etc. | 5/19/2020 |
| 11218 | Abcam Eugene, ON Desktop Support Technician Not specified Exp: 1-2 year(s) |
The Desktop Support Technician will be responsible for providing 1st line IT support to internal Abcam US customers. The ideal candidate will be positive, energetic, and detail oriented while working in a fast-paced environment. Responsibilities: Provides basic support for Windows PCs/laptops, printers, telephones and other IT infrastructure. Installs and configures end user laptops, desktops, and virtual desktop systems. etc. | 5/19/2020 |
| 11219 | Abcam Eugene, ON Research Associate BS in biology or related Exp: 1+ year(s) |
We are seeking a Research Associate to assist in the development of novel homogenous immunoassays in our Eugene, OR facility. The core responsibility will be to provide support to the homogenous immunoassay development team through the use of antibody-based laboratory techniques such as sandwich ELISA, Western blot and flow cytometry as well as the generation of biological materials for analysis. etc. | 5/19/2020 |
| 11220 | Abcam Branford, CT Research Associate, In-House Manufacturing BS in biology or related Exp: 1-3 year(s) |
Abcam is looking for a Research Associate to join our in-house manufacturing team in Eugene. This is a permanent lab-based position which will be responsible for manufacturing, quality testing and assembling our expanding portfolio of products. Etc. | 5/19/2020 |
| 11221 | Acumed Philadelphia, PA Sales Associate - Lehigh Valley BS/BA in a business or medical discipline Exp: 0-3 year(s) |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 5/19/2020 |
| 11222 | Acumed Danville, PA Sales Associate - Danville BS/BA in a business or medical discipline Exp: 0-3 year(s) |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 5/19/2020 |
| 11223 | Acumed New York, NY Sales Associate - NYC - Future Opportunities BS/BA in a business or medical discipline Exp: 0-3 year(s) |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 5/19/2020 |
| 11224 | ABEC Bethlehem, PA Mechanical Designer AS/AA Exp: 1-2 year(s) |
The Mechanical Designer works under the direction of the Design Team Leader and also utilize independent judgment to perform the day-to-day project duties of designing, developing and releasing deliverables. This includes detail & assembly drawings and related bills-of material used in the fabrication of equipment for pilot and commercial scale biopharmaceutical manufacturing (largely pressure vessel assemblies for fluid & gas handling and motorized agitation systems). Primary responsibility involves generating design plans utilizing Autodesk Inventor and AutoCAD software. This position requires a high level of attention to detail along with the ability to develop a strong understanding of the ASME/ BPE Bioprocessing Equipment design standards. etc. | 5/19/2020 |
| 11225 | BioMarin Novato, CA Analyst, QC I (TEMPORARY) BS in biological/chemical sciences Exp: 0-2 years |
Adhere and follow cGMPs guidelines and procedures at all times. Escalate non-compliance concerns to management. Monitor lab equipment for Calibration needs, monitoring and tracking of issues related to instrumentation. Support the scheduled testing by ensuring the required reagents and glassware are stocked appropriately. Maintain the laboratory in an inspection-ready state | 5/17/2020 |
| 11226 | BioMarin Novato, CA Research Assistant BS/BA in biological/physical sciences Exp: 0-2 years |
Primary responsibility is support for the Assay Services subgroup within Analytical Sciences. This position involves performance of a variety of analytical assays with adherence to strict timelines. Assays may include enzyme activity, total protein, cell-based bioassays, chromatography and electrophoresis, done under the supervision of more senior personnel. Assists in the qualification of assay methods and in their transfer to the Quality Control laboratories. Provides major contributions to the evaluation of drug substance and drug product. Receives and records results for Assay Services in support of a variety of different groups including QC, MFG, Cell Culture PD, Purification PD and Formulation. | 5/17/2020 |
| 11227 | BioMarin Brisbane, CA Pharmacovigilance Associate II BS in life scineces Exp: 1year in pharmacovigilance |
Participates in activities related to,and processing of Adverse Events for BioMarin post marketed products and investigational products. Accountable for accurate data capture for individual case safety reports. Responsible for narrative creation for individual case safety reports. Perform quality review (as appropriate) | 5/17/2020 |
| 11228 | BioMarin Novato, CA QC Technician (TEMPORARY) Assocates in sciences Exp: 0-2 years in lab |
The QC In-Process (QCIP) Technician is responsible for supporting microbiological and analytical test methods on in-process intermediates and varying stages of drug products, under supervision and within Current Good Manufacturing Practices (cGMP) guidelines, to support further manufacturing of commercial and clinical therapeutics. | 5/17/2020 |
| 11229 | BioMarin Novato, CA Analyst, QC In-Process BS in related Exp: 0-3 years |
The QC In-Process (QCIP) Analyst is responsible for performing microbiological and analytical test methods on in-process intermediates and varying stages of drug products, under minimal supervision and within cGMP guidelines, to support further manufacturing of commercial and clinical therapeutics. This role will involve knowledge that includes but is not limited to the following analyses and concepts: Protein determination by BCA, Bradford, and UV Absorbance, Enzyme activity, Endotoxin detection, Bioburden quantification, HPLC, Total Organic Carbon, microbial identification and challenge studies, aseptic techniques, and method validation. | 5/17/2020 |
| 11230 | BioMarin Novato, CA Manufacturing Associate (TEMPORARY) BS/BA in sciences or engineering Exp: 0-2 years in biotech |
Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, protein purification and formulation of bulk drug substance. Support initiatives for process optimization | 5/17/2020 |
| 11231 | BioMerics Salt Lake City, UT Injection Molding Machine Operator I, DAY SHIFT HS Diploma/GED Exp: 1-2 years |
Operate plastic injection molding machines. As the Injection Molding Machine Operator you will set up and operate an injection molding machine in order to shape plastics. You will read and interpret blueprints and diagrams to select, position, and secure machinery. This is a hands-on role. | 5/17/2020 |
| 11232 | BioMerics Salt Lake City, UT Injection Molding Machine Operator I, NIGHT SHIFT HS Diploma/GED Exp: 1-2 years |
Operate plastic injection molding machines. As the Injection Molding Machine Operator you will set up and operate an injection molding machine in order to shape plastics. You will read and interpret blueprints and diagrams to select, position, and secure machinery. This is a hands-on role. | 5/17/2020 |
| 11233 | Biomerieux Murray, UT Engineering Tech I Associates in engineering Exp: 0-4 years |
This technician works within a project team under the leadership of project management and other senior engineers. The technician is expected to perform various types of technical activities including testing, verification, operation and manufacturing of prototype medical device consumables. This technician is expected to work and communicate well with other members and leadership of the team in order to meet the goals of the project. | 5/17/2020 |
| 11234 | Biomerieux Durham, NC Manufacturing Tech 1, 3rd shift HS Diploma/GED Exp: 0-1 years |
The Manufacturing Technician position is responsible for the operation of high speed equipment used in the production and packaging of BacT/ALERT bottles and/or preparing and formulating the liquid reagents that fill the finished BacT/ALERT bottle in a cGMP compliant manner. The work hours are Sun-Thurs 11:00PM-7:30AM and occasional OT | 5/17/2020 |
| 11235 | Biomerieux Murray, UT Software Test Engineer I Associate or BS/BA in engineering or computer sciences Exp: 0-3 years |
The software test engineer works aside the software team to assist in producing quality software. This position is responsible for the design, implementation and execution of tests to verify that software and firmware operate correctly and meet design specifications. This individual should work creatively to automate testing where feasible. This individual should have knowledge of one or more programming languages. | 5/17/2020 |
| 11236 | Biomerieux St Louis, MS Production Tech 1 HS Diploma/GED Exp: 1-2 years in FDA regulated manufacturing |
The Production Technician I position is responsible for the operation of high speed equipment used in the production and packaging of VITEK 2 cards in a cGMP compliant manner. The position may perform or assist in the setup, operation, inspection, maintenance, troubleshooting and cleaning of equipment used throughout the VITEK 2 Card Manufacturing and Packaging processes. Additionally, this individual will be responsible for completing production batches and corresponding documentation for the associated tasks, AQL inspections, reworks and material reconciliation that goes along with the batch. Contribute to building a positive work environment. | 5/17/2020 |
| 11237 | BioPharma Services Toronto, On Clinical Research Recruiter BS/BA in sciences Exp: 1-2 years |
Conduct telephone eligibility screening of potential English-speaking volunteers for inclusion or exclusion in all phases of clinical trials which includes but is not limited to, Reviewing screening criteria, Providing an overview of the study,Responding to volunteer preliminary questions, Capturing brief medical and medication history of volunteers, Completion of required paperwork. | 5/17/2020 |
| 11238 | Bio-Rad Hercules, CA Production Tech I - Temp HS Diploma/GED Exp: 0-2 years |
Bio-rad is looking for a Production Tech to produce or supports production of instruments or reagents products in compliance with established GMP procedures and ensures products are of consistent high quality. Acts as part of a technical organizational unit. Maintains instrument documentation, operates a variety of lab and/or engineering/manufacturing test equipment, and troubleshoots and repairs instrument products. (6 positions available.) | 5/17/2020 |
| 11239 | Bio-Rad Woodinville, WA Supply Planner I/II BS/BA in supply chain, business, management Exp: 0-5 years in supply planning/management |
In this role, you will help drive performance of key inventory metrics as well as service levels. Develops a detailed understanding of the supply strategy as well as the global demand and regulatory constraints for assigned finished goods. Utilize SAP for development and communication of finished goods supply plan. Creation of supply plan while coordinating day to day efforts between warehouse locations | 5/17/2020 |
| 11240 | Bio-Rad Pleasanton, CA Research Associate or Senior Research Associate, Assay Development Temp to Hire MS in biological sciences Exp: 0-2 yeares |
You will work in an assay development team on the development of new Research Use Only (RUO) and in vitro diagnostic (IVD) tests for oncology using state-of-the-art droplet digital PCR (ddPCR) technology, in a multi-disciplinary department that includes assay research and development scientists, hardware engineers and software engineers. | 5/17/2020 |
| 11241 | Bio-Rad Hercules, CA Data Analyst I BS/BA in business admin Exp: 0-3 years in database management |
Bio-Rad is looking for a Data Analyst I. The key business projects will include team activities, data analyses and reports development, validation, training, release in Power BI for all identified Customer-Centric Global Supply Chain metrics. Will also support Technical Lead with data automation strategy and initiatives. | 5/17/2020 |
| 11242 | Bio-Rad Woodinville, WA Quality Engineer I BS/BA in sciences Exp: 0-2 years |
Supports project/program activities by performing work with an engineering specialty which involves various types of research, investigations, analysis and interpretation of data. Analyzes nonconformances, complaints and trends to identify and recommend corrective and / or preventive actions. Develops, modifies, applies and maintains methods and procedures for product development, process control, testing and inspection to ensure the manufacturing of safe and effective biotechnological products. | 5/17/2020 |
| 11243 | BioMarin Novato, CA Research Assistant, Sample Coordinator BS/BA Exp: 0-2 years in related |
Primary responsibilities will be to support sample tracking, sample submission, and sample testing coordination for the Analytical Sciences group. This position involves documentation of samples received for analysis from QC, Manufacturing, and other groups within Process Sciences and coordinating with the proper personnel in Analytical Sciences to perform analytical assays with adherence to strict timelines. | 5/17/2020 |
| 11244 | BioMarin Novato, CA Research Assistant Associates or BS/BA in sciences Exp: 0-2 years |
The Analytical Sciences Department is seeking a Research Assistant that will be responsible for coordinating with lab support service providers and multiple departments such as Facilities, EHS&S, Lab Support, IT, Vendors and Contractors to ensure that Analytical Sciences Department needs are met. Performs good documentation practices with instrument and equipment laboratory logbooks and ensures compliance in their documentation. | 5/17/2020 |
| 11245 | BeiGene Cambridge, MA Data Warehouse Analyst BS/BA in data science or health related field Exp: 1-2 years |
The analyst role is responsible to work cross-functionally to support all aspects of data that will be housed in BeiGene’s Data Warehouse. The role will manage data and the related process including but not limited to Real World claims, commercial data and epidemiology data. This role reports to Senior Director, System and Standard. | 5/16/2020 |
| 11246 | BeiGene San Mateo, CA Systems Analyst - Regulatory BS/BA in c omputer science or related Exp: 0-3 years in RD& and pharma tech support |
The Systems Analyst - Regulatory is responsible for providing submission publishing and technical support of the Regulatory systems for BeiGene. This position provides global support to the Regulatory Affairs and Regulatory Operations organizations with an immediate focus of supporting technical projects and regional regulatory filings. This position will collaborate closely with the submission project managers for submissions and the Information Technology team for the Regulatory technology platforms to ensure system and processes are followed in compliance with ISO, FDA, Sarbanes-Oxley and other regulatory requirements. | 5/16/2020 |
| 11247 | Berg Health Framingham, MA Operations Lead – Precision Medicine BS or MS in chemistry or biochemistry Exp: 1-3 years in industry |
Manage project efficiency and timelines across bioanalytical, OMICS, and assay development groups. Coordinate sample extractions and analysis across precision medicine groups. Track and maintain quality control records of instrument analytical performance across groups. Develop project plans and reports for internal and external projects | 5/16/2020 |
| 11248 | Berg Health Framingham, MA Research Associate I – Omics BS or MS in analytical chemistry, biochemistry, or related Exp: 0-2 years |
The Research Associate I will be responsible for biomarker discovery/validation in multiple disease areas, including neurodegenerative diseases, diabetes, obesity, and cancer, using state-of-the-art quantitative proteomics platforms.Assist in high-throughput sample preparation of patient clinical samples in a team-oriented environment | 5/16/2020 |
| 11249 | Berg Health Framingham, MA Research Associate I – Assay Development BS in biology/biochemistry/immunology Exp: 0-2 years |
The successful candidate will execute development studies, conduct data analysis, document results. Assist in ligand binding assay method development (MSD, ELISA) and provide technique and application support for immunoassays transferred to downstream users. Perform experiments to improve assay performance and robustness. Contribute to experimental design, data analysis, critical thinking, and problem-solving to improve methods or procedures. | 5/16/2020 |
| 11250 | Berkshire Sterile Manufacturing Lee, MA Manufacturing Compliance Manager Associates in related Exp: 1 year in lab/manufacturing/quality |
This is a hands-on role responsible for overseeing and managing the investigation and on time closure of process deviations, manufacturing batch record review process, and compiling performance metrics within the manufacturing, visual inspection and materials management functions. Manage the timely review of in process and fully executed batch records against cGMP requirements as well as assist in responding to batch record queries from internal / external sources | 5/16/2020 |
| 11251 | BGI San Jose, CA Laboratory Technician BS in molecular biology Exp: 1-2 years in industry |
As a member of the BGIA Support team, the position will support next generation processes for genome sequencing. The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. | 5/16/2020 |
| 11252 | BioAgilytix Durham, NC QA Auditor BS/BA in biology/chemistry or related Exp: 1-3 years in industry |
Perform Quality Assurance (QA) audits, inspections (internal/external) and monitoring procedures against standard operating procedures, methods, protocols/plans, guidances, and/or regulations, as applicable. Assist in hosting regulatory inspections by acting as scribe and/or reviewing documents and identifying and calling operational staff to answer questions as required | 5/16/2020 |
| 11253 | BioAgilytix Durham, NC Laboratory Support Technician | Purchasing Agent Associates in biology/biotechnology Exp: 1+ years in lab |
The Laboratory Support Technician | Purchasing Agent is responsible for laboratory support and purchasing for Operations. This includes processing purchase orders with vendors, matching packing slips with purchase orders, and overall tracking of reagent receipts in NetSuite. | 5/16/2020 |
| 11254 | BioAgilytix Durham, NC Analyst BS/BA in biological sciences/technology Exp: 1 year in lab |
Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export) | 5/16/2020 |
| 11255 | BioAssay Systems Hayward, CA Research Associate - Assay Development BS/BA in biological/chemical sciences Exp: 1-2 years in lab |
This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers. | 5/16/2020 |
| 11256 | BioAssay Systems Hayward, CA Research Associate - Manufacturing BS/BA in biological/chemical sciences Exp: 1-2 years in lab |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing, and packaging the finished products. This candidate may also join part time in our R&D team. | 5/16/2020 |
| 11257 | Bioclinica Newark, CA Auditor I, Medical Imaging Associates in life sciences or quality management or computer sciences Exp: 0-3 years in QA |
Plans, conducts, and reports audits according to Bioclinica’s standard operating procedures (SOPs) and electronic document management system (EDMS) processes. Tracks and/or trends audit issues and/or CAPAs until closure. Provides root cause guidance to CAPA owners and/or conducts root cause analysis when assigned. Ability to work with all levels of Bioclinica personnel and external personnel in a professional and organized manner. | 5/16/2020 |
| 11258 | Bioclinica Durham, NC Software Engineer I BS/BA preferred Exp: 1+ years in software development |
This role analyzes, designs, programs, debugs, and modifies software enhancements and/or new products used in local, networked, or Internet-related computer programs. Code is used in applications that variously support Bioclinica’s radiologists, clinical data managers, operations staff, clients and partners. Using current programming language and technologies, writes code, completes programming, and performs testing and debugging of applications. | 5/16/2020 |
| 11259 | Biodesix Port Richey, FL Mobile Phlebotomist Certification for Phelbotomy Exp: 1 year performing draws |
This is a contract position, terms of net 30. Must provide own gloves and sharps container. Must have access to disposal service. MP will go to client's home or place of work to perform draw. MP will be responsible for scheduling their own appointments based on information provided from Biodesix. You must complete scheduling within 24 hours of assignment. | 5/16/2020 |
| 11260 | Biodesix New Haven, CT Mobile Phlebotomist Certification for Phelbotomy Exp: 1 year performing draws |
This is a contract position, terms of net 30. Must provide own gloves and sharps container. Must have access to disposal service. MP will go to client's home or place of work to perform draw. MP will be responsible for scheduling their own appointments based on information provided from Biodesix. You must complete scheduling within 24 hours of assignment. | 5/16/2020 |
| 11261 | Biodesix Boulder, CO Document Control Specialist BS/BA in realted Exp: 0-2 years in quality |
The Document Control Specialist is responsible for quality assurance and compliance of the Document Control program, Training program, and management of laboratory notebooks throughout product lifecycle. This role is responsible for ensuring all documentation, DHFs and records are structured and organized in accordance with the document control and training procedures. This is a dedicated, service-oriented resource to manage the process, improve system maintenance, develop meaningful, proactive metrics and assist with functional groups to ensure the work is of quality standards but allows them to focus on their critical tasks. | 5/16/2020 |
| 11262 | Biodesix De Soto, KS Laboratory Technician BS/BA in chemical, physical or biological sciences Exp: 0-2 years in lab |
Laboratory technicians assist with the setup and support of the daily activities of the laboratory. In addition, Laboratory Technicians have the technical training and experience required to perform regulated clinical laboratory test realization (test specimen receipt through test result generation) using standard in-vitro laboratory techniques. | 5/16/2020 |
| 11263 | Bioduro San Diego, CA Research Associate II, Oncology BS in biological sciences Exp: 1 year in lab |
The Research Associate is responsible for implementation of in vivo and in vitro studies through animal handling in a vivarium or laboratory environment; including compound administration by multiple routes – dosing, tumor implantation and measurement, harvesting tissues and blood samples. Accurately perform in vivo studies that include the following laboratory procedures: Tumor implantation and measurement, mouse dosing, blood sampling and tissue harvesting and processing | 5/16/2020 |
| 11264 | BioFire Salt Lake City, UT QC Technologist I/II - Swing Shift Associates for life sciences Exp: entry level |
Perform all work in compliance with company policy and within the guidelines of Biofire Diagnostic’s Quality System. Responsible for performing quality control testing on incoming reagents use in Film Array. Responsible for maintaining supply stocks as well as coordinating instrument/equipment repairs as necessary. Responsible for all pipet calibrationsand the Artel system calibration. | 5/16/2020 |
| 11265 | BioFire Salt Lake City, UT BioReagents Formulator - Day Actively enrolled in 2 year degree Exp: 1+ years in lab |
This is a full-time non-exempt position. Responsible for manufacturing and formulation of all BioReagents products and sub-assemblies including FilmArray. Operates production equipment and performs duties under compliance of cGMP manufacturing. Weighs, measures, and checks raw materials to assure that manufactured batches, lots, buffers and sub-assemblies contain the proper reagents and qualities. Has knowledge of commonly used concepts, practices, and procedures including PCR, real-time PCR, and use of fluorescence based nucleic acid detection techniques. | 5/16/2020 |
| 11266 | BioFire Salt Lake City, UT Instrument Manufacturing Technician I / Trainee HS Diploma Exp: 0+ years |
Utilizing attention to detail, the Instrument Production Technician I operates production equipment and assembles instrument components using fine motor dexterity. Responsible for performing a wide variety of electronic or electro-mechanical assembly operations on sub-assembly components. | 5/16/2020 |
| 11267 | BioFire Salt Lake City, UT Financial Analyst I BS/BA in accounting, finance, information systems Exp: 1+ years in accounting |
This position assists with financial variance analysis, compiles data for reporting, and assists with models for trending and forecasting. Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics’ Quality System. Monitor revenue transaction to ensure proper coding of transactions. Maintains sales and installed base reports and dashboards. | 5/16/2020 |
| 11268 | BioFire Salt Lake City, UT Inventory Control Analyst I HS Diploma/GED Exp: 1+ years in warehouse |
Position will provide quick response to supply chain, quality, and production teams’ to resolve variances. Takes daily proactive measures to ensure a high degree of inventory accuracy. When necessary, will monitor internal MES and ERP queues, will identify and document queue errors, will analyze errors for root cause, and will resolve errors with appropriate action. | 5/16/2020 |
| 11269 | BioGX Birmingham, AL Reagent Production Technician I BS in biology or engineering Exp: 0-2 years |
The Manufacturing Technician is responsible for general laboratory duties focused on manual and automated filling andpackaging of standards,controls and panels for commercically avalible nucleic acid tests and other advanced reagents. The Manufacturing Technician is expected to follow standard operating procedures and quality systems documentation in a GMP environment | 5/16/2020 |
| 11270 | Biolife Solutions Albuquerque, NM Product Testing Technician HS Diploma/GED Exp: No experience required |
Filling, weighing and pouring off Dewars that weigh 85 lbs. Perform and assist with data recording of measurements. Maintain accurate testing and sanitation documentation as needed and required by the standard operating procedures | 5/16/2020 |
| 11271 | BioFire Salt Lake City, UT Material Handler I HS Diploma/APICS training Exp: No experience required |
The Material Handler I is responsible for the physical movement, support, and administrative tasks involved in receiving, shipping, storing, and support of raw material used for manufacturing of good. Perform real time daily replenish of material to the floor in a “Just in Time” manner to never run the line dry, yet to also ensure inventory is minimized in the line. Break down, clean, organize, and prep raw material ready for manufacturing in accordance to procedure and production requirements. | 5/16/2020 |
| 11272 | Biogen Cambridge, MA Engineer I, Purification Process Development, Gene Therapy BS or MS in biological/chemical engineering or sciences Exp: 0-2 years |
The successful candidate will join a team of engineers/scientists responsible for the development of purification processes used for the clinical and commercial manufacture of adeno-associated viral (AAV) vectors. This individual will be involved in execution of multiple aspects of viral vector purification, including chromatography, filtration and membrane separations (TFF, UFDF, microfiltration, viral filtration, and depth filtration), and validation of viral and contaminant clearance. In addition, the individual may participate in project teams and in the scale-up and technology transfer of purification processes to the manufacturing organizations. | 5/16/2020 |
| 11273 | Biogen Research Triangle Park, NC Manufacturing Associate (Parenteral Filling Facility) HS Diploma, BS/BA preferred Exp: 0-2 years |
In this role you will be responsible for performing and documenting daily manufacturing operations in a cGMP environment. This involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments. Applicants will be highly detailed oriented with excellent documentation skills. Applicants will become trained and skilled at most or all unit operations in their area, often leading the execution of procedures, and performs most functions with minimal supervision. | 5/16/2020 |
| 11274 | Biogen Research Triangle Park, NC Patient Services Coordinator BS/BA Exp: 1-2 years |
The primary role of the Patient Service Coordinator is to facilitate the customer lifecycle by assisting patients, healthcare providers and others with activities related to starting and staying on therapy. Patient base includes both newly diagnosed and existing Alzheimer patients. Daily interactions involve contact via phone not only with patients but also health care providers, Biogen field force representatives, business service partners, nursing services and other internal work groups. | 5/16/2020 |
| 11275 | Vividion San Diego, CA Research Associate, Molecular and Cellular Biology BS/MS in cell biology Exp: 0-3 years |
The successful candidate will have extensive hands on experience and expertise in basic molecular biology, mammalian cell culture techniques, and cellular and biochemical assay development. They will support the validation of novel drug targets via multiple mechanisms, including testing the effects of compounds on proteins in cellular and biochemical settings. They will utilize the development and/or use of new technology to support drug discovery. etc. | 5/13/2020 |
| 11276 | TA Instruments New Castle, DE Embedded Software Engineer MS in computer or electrical engineering Exp: 0-3 years |
TA Instruments is known for its innovation and quality in its analytical instrumentation and is looking for an embedded Software Development Engineer for our Development Engineering Thermal Analysis Group to support its world-class reputation. This is a career-level opportunity for an innovative, creative, scientific engineering mind to take their software, electrical engineering, or computer science/engineering background and apply it in an engineering development environment to create new systems to make better measurements for scientists and engineers around the world to use to develop new and better products. etc. | 5/13/2020 |
| 11277 | TA Instruments Rockville, MD Training Specialist BS/BA in education or social science Exp: 1 year |
Westat has an immediate opening for a Training Specialist with experience in developing adult learning training materials. The successful candidate will work closely with project managers and a multidisciplinary research team working on data collection for the National Assessment of Educational Progress, (NAEP), an innovative digital educational assessment also known as “The Nation’s Report Card.” Job Responsibilities: Participate in design, development and review of distance training development program. Create training materials including developing and writing training procedures manuals and support material. etc. | 5/13/2020 |
| 11278 | Worldwide Clinical Trials Morrisville, NC Clinical Operations Assistant BS Exp: 1+ year(s) |
The Clinical Operations Assistant is a full-time position responsible for completing all assigned projects for Clinical Operations in a timely and accurate manner while interfacing directly with in-house personnel and field employees. Key functions include management of essential document submission to Trial Master Files, supporting field personnel with Microsoft Office, and providing additional administrative support when time permits. RESPONSIBILITIES: Manage and track document flow of essential documents from investigator sites to the Trial Master Files. etc. | 5/13/2020 |
| 11279 | Worldwide Clinical Trials San Antonio, TX Facilities Technician HS diploma or equivalent Exp: 1+ year(s) |
Tasks may include but are not limited to: Assists with building upkeep, upgrades, and ordering of any furnishings as needed. Performs or assists with repairs on buildings, grounds, and equipment. Assists the Facilities Coordinator with training other PRN Facilities Technicians on these duties. Oversees equipment inventory, repairs, maintenance checks, and documentation. Shops for supplies as appropriate. Escorts vendors in all subject areas and areas where confidential documents are maintained. etc. | 5/13/2020 |
| 11280 | Worldwide Clinical Trials Austin, TX Lab Assistant HS diploma or equivalent Exp: 1-3 year(s) |
Tasks may include but are not limited to: Responsible for the storage and retrieval of study samples at Worldwide. Maintain an inventory of samples for easy retrieval. Keep sample storage freezers organized and clean. Log-in study samples. Facilitate the removal and return of study samples from Worldwide’s freezers during samples analysis. Ensure that study samples are archived, returned to the sponsor and/or disposed of when appropriate. etc. | 5/13/2020 |
| 11281 | Wright Medical Indianapolis, IN Associate Sales Representative, Upper Extremities - Indianapolis, IN BS/BA Exp: 0-2 years |
Wright Medical is currently hiring an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This position is a field based position. etc. | 5/13/2020 |
| 11282 | Wright Medical Fresno, CA Associate Sales Representative, Upper Extremities - Fresno, CA BS/BA Exp: 0-2 years |
Wright Medical is hiring an Associate Sales Rep in Fresno, CA. This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is a field based position. In anticipation of future needs. etc. | 5/13/2020 |
| 11283 | Wright Medical Fresno, CA Associate Sales Representative, Lower Extremities & Biologics - Fresno, CA BS/BA Exp: 0-2 years |
Wright Medical is currenting hiring an Associate Sales Representative. This position will require you to learn our products, market and industry. This role will support our foot & ankle and biologics portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is a field based position. Your Focus: Conducts regular sales calls in person to develop customer relationships and follow up on leads in order to promote, market and sell products. etc. | 5/13/2020 |
| 11284 | Wright Medical Houston, TX Associate Sales Rep, Upper Extremities - Houston, TX BS/BA Exp: 0-2 years |
Wright Medical is hiring an Associate Sales Rep. This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is a field based position. etc. | 5/13/2020 |
| 11285 | Wright Medical San Jose, CA Associate Sales Representative, Upper Extremities - Northern California BS/BA Exp: 0-2 years |
This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This position is a field based position. etc. | 5/13/2020 |
| 11286 | Wright Medical Lexington, KY Associate Sales/BluePrint Field Marketing Specialist, Upper Extremities - Lexington, KY BS/BA Exp: 0-2 years |
Wright Medical is hiring an Associate Sales Field Marketing Manager is responsible for downstream marketing support of Wright’s BLUEPRINT Virtual Surgery platform. This position will provide field-based clinical expertise, software/I.T. support, training and education, targeted product launch execution, and strategic initiative support to customers, sales representatives, and CT scan centers. The expectation of this role is to be a sales, technical and clinical expert for Wright’s BLUEPRINT platform. etc. | 5/13/2020 |
| 11287 | Wright Medical New York, NY Associate Sales Representative, Upper Extremities - New York, NY BS/BA Exp: 0-2 years |
Wright Medical is hiring an Associate Sales Rep. This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. etc. | 5/13/2020 |
| 11288 | Xellia Cleveland, OH EM Specialist I - Night Shift (12 Hours) BS in microbiology or other science Exp: 1-5 year(s) |
The Aseptic Environmental Monitoring Specialist I position works closely with other departments, such as Operations, Maintenance, Quality Assurance, Validation, and Engineering to assure the support of the Environmental Monitoring department on various projects, studies and routine tasks. The individual holding the position of Environmental Monitoring Specialist I shall be responsible for performing routine and non-routine testing. They will be responsible for Environmental Monitoring documentation and corrections. The individual will assist with the training of environmental monitoring personnel on tests and methods. etc. | 5/13/2020 |
| 11289 | Xellia Cleveland, OH Microbiologist - 2nd Shift BS in biology, biochemistry, biotechnology, or related Exp: 0-2 years |
The Microbiologist supports the testing in the Microbiology laboratory at the Xellia Cleveland site. In this role, the Microbiologist I is responsible for will be responsible for all aspects of the Microbiology laboratory operations, such as sample receipt, sample testing, data generation, data analysis and summarization and other QC lab supporting activities. Uses good documentation practices in the collection of data/records. Authors and executes qualification documents, SOPs, protocols, and investigations. Recommends corrective actions or process improvements that will eliminate the potential for laboratory deviations. etc. | 5/13/2020 |
| 11290 | Xellia Cleveland, OH Sterile Operations Supervisor - RTU Manufacturing BS Exp: 0-5 years |
Position is primarily the direct supervision of manufacturing Aseptic Operators; ensuring sterile injectable pharmaceuticals are manufactured in strict adherence to cGMPs ensuring safety, quality, and potency of the product produced. Sterile Operations Supervisor is also the first level of management that ensures adherence to the production plan and delivery of On Time In Full targets. etc. | 5/13/2020 |
| 11291 | Xellia Cleveland, OH Manufacturing Quality Assurance Specialist I AS/BS in a life or physical science Exp: 1+ year(s) |
The Manufacturing Quality Assurance (MQA) Specialist I is responsible for providing quality oversight to all manufacturing and packaging areas to ensure product quality and SOP/GMP compliance at the Cleveland Manufacturing Facility. Works closely with Production personnel to complete on-the-floor, in process batch record review, resolve all batch related issues or escalate to the Quality Assurance Supervisor as appropriate, and ensure good documentation practices are being followed. etc. | 5/13/2020 |
| 11292 | Xellia Cleveland, OH Aseptic Operator I - 12 Hour Shift HS diploma/AS Exp: 0-1 year(s) |
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator I is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. etc. | 5/13/2020 |
| 11293 | Xellia Cleveland, OH Aseptic Operator II - 12 Hours HS diploma/AS Exp: 1-2 year(s) |
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator II is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. etc. | 5/13/2020 |
| 11294 | ZeteoTech Sykesville, MD Microbiologist BS in microbiology, biology, biochemistry, or related Exp: 1-5 year(s) |
Zeteo Tech, Inc, a venture backed company developing solution for Medical and Biodefense applications, is seeking a motivated microbiologist to join our team. The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your expertise to conduct biological laboratory tests to assist scientists in development of tools to detect and decontaminate biological organisms and materials. This is an entry-level position with room for growth. etc. | 5/13/2020 |
| 11295 | Zoetis Charles City, IA Quality Scientist I – Media Prep AA/BS/BA Exp: 0-1 year(s) |
This Quality Scientist I will prioritize daily tasks to ensure that medias and chemical solutions are prepared in accordance to their respective batch records and completed in an accurate and timely manner. Clean, wrap and label lab glassware and equipment. Support testing labs and ensure timely completion of tests to meet the established lead times. Following GMP documentation guidelines. Basic problem solving skills and demonstrate trouble shooting ability. Contribute to the teams productivity goals. Colleague should have ability to follow detailed instructions and perform basic math calculations. etc. | 5/13/2020 |
| 11296 | Zoetis Lincoln, NE Sterilization Technician HS diploma/AS Exp: Not required |
Perform routine glassware preparation, washing and sterilization in compliance with specified Standard Operating Procedures. The position will also perform various other support functions including but not limited to supplies inventory, general cleaning and sample retrieval. Adhere to Standard Operating Procedures and perform all duties in a safe manner. etc. | 5/13/2020 |
| 11297 | Zoetis Lincoln, NE Packaging Technician – 3rd Shift HS diploma/AS/AA Exp: 6 months |
Working with a coach and / or trainer complete the Packaging Operations On the Job Training Program which includes, but is not limited to the following: Complete Training Modules (Packaging Orientation, Packaging Safety, Packaging Safety Program, Packaging Colleague Expectations, and the department specific module for the packaging area assigned). Complete job-specific training checklists for 5 packaging lines. Learn to use Packaging related Standard Operating Procedures, Batch Records, Log Books and Job Aides. Learn the operation of Motorized Materials Handling Equipment as assigned. etc. | 5/13/2020 |
| 11298 | Zoetis San Diego, CA QC Associate Scientist I BS in a biological or other life science Exp: 1+ year(s) |
This individual must have a solid understanding of immunoassays, their principles of performance, and demonstrate the ability to run or conduct all principle in-house assays consistently and independently in the QC lab. POSITION RESPONSIBILITIES: Schedules, performs, and reports routine assays including in-process, final, stability, and various anti-serum screening assays, bringing to the attention of their supervisor any unanticipated or unusual results. Responsible for all raw material and reagent testing. LAL testing and gram-staining is performed occasionally. As needed, this individual will perform qualification testing for all new in-house reference standards. etc. | 5/13/2020 |
| 11299 | 10x Genomics Pleasanton, CA Research Associate 2-Molecular Biology/Product Development MS in molecular biology, genetics, analytical chemistry, or related Exp: 1+ year(s) |
We are seeking an outstanding Research Associate to join the Product Development team to support the development and commercial launch of new products. This is a unique cross-disciplinary position that will work closely with a variety of groups including Molecular Biology, Chemistry, Microfluidics, QC, and Manufacturing, to develop and validate novel reagents for the rapid expansion of 10x product lines. Candidates must have a broad working knowledge of molecular biology and be able to apply that knowledge creatively and independently in a fast-paced work environment. The successful applicant will have exceptional attention to detail and the ability to meticulously execute and analyze highly complex experiments. Previous industry experience is essential. etc. | 5/13/2020 |
| 11300 | 1910 Genetics Cambridge, MA Research Associate - Biology BS/MS in biology, biochemistry, pharmacology or related Exp: 0-3 years |
Your key responsibilities will include… Executing high throughput screening (HTS) assays in strict accordance with the NIH NCATS Assay Guidance Manual. Developing and validating HTS biochemical assays for characterizing the activity and selectivity of potential drug candidates. Developing and validating HTS cell-based assays for characterizing the activity, selectivity, and cellular permeability of potential drug candidates. Performing a wide variety of experiments across molecular biology, cell biology, biochemistry, in vitro pharmacology, and in vivo pharmacology. etc. | 5/13/2020 |
| 11301 | WuXi AppTec King of Prussia, PA Scientist I Downstream Process Development BS/MS Exp: 0-5 years |
Responsibilities: Work independently on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. Design and execute lab-scale experiment in supporting downstream process development, verification, characterization. Perform purification experiments in BSL-2 labs and document experiments in lab notebooks. etc. | 5/13/2020 |
| 11302 | WuXi AppTec Cranbury, NJ Associate Scientist II MS/MA Exp: 0 years |
Essential Job Functions: Under minimal supervision, individual performs routine laboratory techniques and more difficult procedures, including but not limited to weighing the chemical, preparing the stock solution and standard calibrator/QC in biological fluids, extracting the samples, analysing the samples, summarizing the data, and etc. Receives specific instructions on assigned task and expected results. Delivers accurate results on assigned tasks within the expected timeframe. May assume the duty as a trainer to new hires. Has a thorough understanding of the study and method; troubleshoots unexpected results. etc. | 5/13/2020 |
| 11303 | WuXi AppTec King of Prussia, PA Scientist, Upstream Process Development BS/MS Exp: 1-2 year(s) |
Responsibilities: Work on defined biopharmaceutical projects for development and/or characterization of vaccine upstream manufacturing cell culture processes. Perform bench scale and pilot scale bioreactor operations in supporting upstream process development, verification, characterization, and tech transfer. Perform data analysis and interpretation, and develop strategies for optimization and troubleshooting. Support technical transfer of processes into the non-GMP pilot plant or GMP production facility. Keep accurate record of cell culture parameters and results into datasheets and/or laboratory notebooks. etc. | 5/13/2020 |
| 11304 | WuXi AppTec St. Paul, MN Facilities Technician HS diploma or equivalent Exp: 1-2 year(s) |
Performs facilities duties in compliance with applicable procedures, regulations, and industry standards to support building/laboratory infrastructure and testing/manufacturing operations. Supports continuous improvement initiatives at the Saint Paul, MN facility. Responsibilities: Essential Job Functions: Complete preventative maintenance of equipment, systems, and buildings. Complete non-routine (troubleshooting, repair) maintenance of equipment, systems, and buildings. etc. | 5/13/2020 |
| 11305 | WuXi AppTec Philadelphia, PA Laboratory Technician II BS in a biological science or related Exp: 1-2 year(s) |
Performs virology, safety, and gene therapy assays according to testing records and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), and Standard Operating Procedures (SOPs). Responsibilities: Maintain cell cultures in accordance to SOPs and testing records. Conduct assays and lab procedures as outlined in testing record and regulatory guidelines. Conducts PCR and ELISA assays. Works in BSL2 lab setting using virus positive controls. | 5/13/2020 |
| 11306 | WuXi AppTec Cranbury, NJ Associate Scientist I BS Exp: 1+ year(s) |
We are searching for an Associate Scientist to join our growing HTS and in vitro screening team. Responsibilities: Requiring daily supervision to participate in the processes of in vitro assay screening and high throughput screening (HTS) of a wide array of protocols for a diverse client base that includes pharmaceutical and biotechnology companies. Works on assignments with a diverse team of scientists to facilitate all aspects of performing in vitro screening and running an HTS laboratory. etc. | 5/13/2020 |
| 11307 | WuXi AppTec San Diego, CA Analytical Lab Assistant HS diploma/BS in chemistry or biochemistry Exp: 1 year |
The Analytical Lab Assistant is responsible for providing support to scientists with lab tests and research. The incumbent receives, stores and distributes supplies, assists with pre-analytical, analytical and post-analytical test processes, and other related tasks. Responsibilities: Orders, receives, stores and distributes supplies. Keeps work areas stocked and cleaned. etc. | 5/13/2020 |
| 11308 | Eurofins Cambridge, MA Laboratory Operations Associate BS Exp: 0-2 months |
Job Description: Performing routine lab operations including maintenance, tracking, and life cycle management of laboratory equipment. Monitoring of equipment alarm system and coordinating equipment preventive maintenance/repairs with asset management and scientific staff. Assisting in general lab housekeeping. Interfacing with EHS, Facilities, Asset Management, and scientific staff on routine operations and on continuous improvement efforts for optimal operating efficiency. Participating in lab inspections to ensure compliance and safety. Assisting with new equipment assessment and installation and on additional lab related projects as they arise. etc. | 5/13/2020 |
| 11309 | Eurofins Nashville, TN HPLC Technician MS in chemistry Exp: 1-2 year(s) |
Employee Responsibilities: Support the analytical testing for process development. Chemical labeling of biological samples, HPLC separation, and data analysis. Preparing buffers, setting up, sterilization, sampling, and cleaning of systems. Document laboratory activities manually and electronically and enter process data into database. Troubleshoot equipment and perform minor repairs. Perform review and peer review of analytical data. etc. | 5/13/2020 |
| 11310 | Eurofins West Point, PA PCR Assay Scientist BS/BA in biology, chemistry, biomedical engineering or related Exp: 6+ months |
Assay Scientist responsibilities include, but are not limited to, the following: The development and performing of assays to support biopharmaceutical testing. Prepare and pipet small volume solutions. Maintain records and test results following good manufacturing practices (GMP). Document work clearly and perform tests accurately. Perform tasks in a repeatable and efficient manner. Communicate effectively with team members and client staff. etc. | 5/13/2020 |
| 11311 | Eurofins Lancaster, PA Molecular and Cell Scientist II: Method Development and Validation MS in molecular or cell biology or related Exp: 1-2 year(s) |
Job Description: Perform a wide range of analyses (routine and non-routine)to support biopharmaceutical testing. Analyses are primarily, but not limited to, cell-based assays and ELISA's (kit-based and de novo). Meet TAT for assigned testing/projects and work independently. Review and evaluate raw data for acceptability. Assist other technical staff in evaluation of raw data for acceptability. Contribute to the development and validation of methods used within the department.. Be able to plan and organize work week and communicate schedule to management when required. Attend client facing meetings as needed. etc. | 5/13/2020 |
| 11312 | Eurofins Lancaster, PA Associate Stability Project Management Specialist/Scientist BS/BA in science, business, or related Exp: Not necessary for BS/BA candidates |
Job Description: Manage all aspects of stability studies submitted by assigned clients. Take responsibility for quality and TAT of assigned studies. Writing stability protocols. LIMS entry for stability studies. Potential to move into a lab role within 12 months as workload shifts. etc. | 5/13/2020 |
| 11313 | Eurofins Indianapolis, IN Analytical Chemist - Night Shift BS in chemistry, biology, or related Exp: 3+ months |
Employee Responsibilities: Perform biochemical testing on proteins and antibodies including, but not limited to, CE, IC, HPLC, SEC, SDS-PAGE, UV, Protein A titer, ELISA, and Particulates. Working as part of a team in a rotating night shift role (shift pattern of 3-2-2-3) which includes working weekends and holidays when they fall within shift pattern. Enter data into LIMS. Ability to work independently and as part of a team in a GMP environment. Participate in conducting investigations. etc. | 5/13/2020 |
| 11314 | VRL Eurofins Centennial, CO Warehouse Associate HS diploma or equivalent Exp: Not required |
Headquartered near Denver, Colorado, with satellite laboratories in or near Los Angeles, Dallas, Boston, Atlanta, and Minneapolis, VRL Eurofins is continuing to expand throughout the United States and is seeking a highly motivated and detail oriented Warehouse Associate to work in Centennial, CO. Job Description: Warehouse Associate responsibilities include, but are not limited to, the following: Oversee all inbound supply deliveries. Performs receipt inspections and enters received goods into receiving system per SOP. etc. | 5/13/2020 |
| 11315 | Terumo Elkton, VA Quality Operations Engineering Technician HS diploma Exp: 1-3 year(s) |
This position is responsible to support all activities related to Quality Operations. QE Technicians will support activities including, but not limited to: non-conforming product activities, investigation of failures, test method validations, procedure updates, training, and other departmental operating activities. Job Details: 1. Perform activities associated with the non-confirming product process: identification, containment, segregation, and evaluation. 2. Perform failure investigations with limited scope and routine analysis. 3. Execute activities associated with inspection methods: calibration, training, TMV execution 4. Perform data collection and limited data analysis. 5. Execute procedure updates with guidance from supervisor. 6. Coordinate calibration activities as necessary. etc. | 5/6/2020 |
| 11316 | Teva Salt Lake City, UT Metrologist I BS in chemistry, engineering, or related Exp: 0+ years |
Under close supervision, calibrates and maintains laboratory instruments as specified in Standard Operating Procedures (SOP's), ensures that completed tasks are documented as specified in the SOP's, and performs related duties as assigned. Essential Job Functions: This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities. Incumbent(s) may not be required to perform all duties listed, and may be required to perform additional, position-specific tasks. Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws. Calibrates instruments in accordance with SOPs. Performs routine preventative maintenance on instruments as per written procedures. etc. | 5/6/2020 |
| 11317 | ThermoFisher Scientific Millersburg, PA Manufacturing Supervisor - 3rd Shift HS diploma or equivalent Exp: 1 year |
Responsibilities: Process Management by simplifying complex processes; getting more out of fewer resources; understand how to separate and combine tasks into efficient workflow. Develop direct reports by providing challenging tasks and assignments; provide developmental feedback. Direct others through establishing direction; distribute workload; clear communication. Managing & Measuring work by tracking and assigning responsibilities for tasks; set clear objectives and provide feedback. etc. | 5/6/2020 |
| 11318 | Tolmar Fort Collins, CO Manufacturing Technician I - Aseptic (2nd Shift, Wed - Sat) HS diploma or equivalent Exp: Not required |
Key Responsibilities: Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of "Right the First Time". Record data in notebooks or lab forms and accurately calculate results to support process. Perform job in a clean room environment requiring clean room gowning, including but not limited to: Company-provided Scrubs. Shoe Covers and Sterile boot covers. Hairnets (and beard covers as applicable). etc. | 5/6/2020 |
| 11319 | Tolmar Fort Collins, CO Manufacturing Technician I - Aseptic (2nd Shift, Sun - Wed) HS diploma or equivalent Exp: Not required |
Key Responsibilities: Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of "Right the First Time". Record data in notebooks or lab forms and accurately calculate results to support process. Perform job in a clean room environment requiring clean room gowning, including but not limited to: Company-provided Scrubs. Shoe Covers and Sterile boot covers. Hairnets (and beard covers as applicable). etc. | 5/6/2020 |
| 11320 | Tolmar Fort Collins, CO MF Technician I - Inject HS diploma or equivalent Exp: Not required |
The Injectable Technician I provides general support for the manufacturing department with a focus on injectable products, while ensuring that our products are made with quality for our patients. Essential Duties & Responsibilities: Perform job in a clean room environment requiring clean room gowning. Assist in the set up and operation labeling equipment used to label pre-filled syringes and/or vials, including equipment in the sterile support areas. Assist in the set up and operation of semi-automatic packaging equipment used to package pre-filled syringes. etc. | 5/6/2020 |
| 11321 | Tolmar Windsor, CO Manufacturing Technician I - Aseptic (2nd Shift, Mon - Thurs) HS diploma or equivalent Exp: Not required |
The Aseptic Technician I provides general support for the manufacturing department with a focus on injectable products, while ensuring that our products are made with quality for our patients. Key Responsibilities: Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of "Right the First Time". Record data in notebooks or lab forms and accurately calculate results to support process. etc. | 5/6/2020 |
| 11322 | Tolmar Windsor, CO Manufacturing Operator I - Polymer - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
The Polymer Operator performs routine activities related to supporting the polymer team, while ensuring that products are made with quality and in accordance with Good Manufacturing Practices. Essential Duties & Responsibilities: Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of “Right the First Time.” Perform job in a clean room environment requiring clean room gowning, including but not limited to: Company-provided Scrubs. Shoe Covers and Sterile Boot Covers. Hairnets (and beard covers as applicable). etc. | 5/6/2020 |
| 11323 | Tolmar Fort Collins, CO MF Technician I - Derms HS diploma or equivalent Exp: Not required |
The Manufacturing Technician I provides general support for the manufacturing department with a focus on dermatology products, while ensuring that our products are made with quality for our patients. Key Responsibilities: Perform job in a clean room environment requiring clean room gowning. Assist in the setup of all final packaging equipment (cartons). Properly load subcomponents into final packaging equipment. Accurately document production activities using regulatory controlled documents including production records and log books. etc. | 5/6/2020 |
| 11324 | Tolmar Fort Collins, CO Manufacturing Operator I - Derm HS diploma or equivalent Exp: 1+ year(s) |
The Manufacturing Operator I performs routine activities related to supporting the dermatology team, while ensuring that products are made with quality for our patients. Key Responsibilities: Perform job in a clean room environment requiring clean room gowning. Assist in the setup/operation/disassembly and cleaning of production filling equipment. Perform routine sampling and inspections for product attributes (fill weights, product sealing, labeling) of filled products. Assist in the setup/operation/disassembly of packaging equipment. etc. | 5/6/2020 |
| 11325 | TriLink Biotechnologies San Diego, CA Quality Assurance Associate I BS in a scientific discipline Exp: 0-3 years |
TriLink BioTechnologies is seeking Quality Assurance Associate I to join our growing team. This role is responsible for review and approval of material release specifications, raw materials, intermediates and consumables in compliance with cGMP regulatory requirements and ISO standards. This role will provide support for other functions performed by QA operations group. Responsibilities: Responsible for conducting raw material, component, in-process inspection and release in conformance to established product requirements. etc. | 5/6/2020 |
| 11326 | Tris Pharma Monmouth Junction, NJ QA Inspector HS diploma or equivalent Exp: 1+ year(s) |
The Quality Assurance (QA) Inspector is responsible for performing in-coming inspections of all raw material/components, performing in-process inspections, providing clearance for rooms/lines to run and ensuring adherence to company Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs) and batch record specifications. Responsibilities include, but not limited to: Identify any non-conforming material and control status of materials during in-coming inspection. Identify any in-process failures during in-process inspections. etc. | 5/6/2020 |
| 11327 | Twist Bioscience South San Francisco, CA Research Associate, Process Development MS in molecular biology, biochemistry, or genetics Exp: 1+ year(s) |
We are seeking an outstanding, innovative, and creative Research Associate to join our team in South San Francisco. The Research Associate will interface between R&D and Operations to establish new processes at scale for DNA-based products in manufacturing. You will develop and support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput probe generation through robust experimental design. The ideal candidate will be driven and will do what it takes to keep manufacturing on track and constantly improving in a fast paced startup environment. etc. | 5/6/2020 |
| 11328 | Twist Bioscience South San Francisco, CA Manufacturing Associate, Single Variant Libraries BS/AS in biology, chemistry, or biochemistry Exp: Not necessary for degree candidates |
The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. Roles and Responsibilities include but are not limited to: Manufacture high quality custom oligo containing products in a high throughput MFG lab according to established SOPs. etc. | 5/6/2020 |
| 11329 | Twist Bioscience South San Francisco, CA Manufacturing Associate, Maxi Prep BS/AS in biology, chemistry, or biochemistry Exp: Not necessary for degree candidates |
The Manufacturing Associate, Maxi Prep will be accountable for following scheduled tasks, Exhibit detail-oriented documentation skills for updating batch records and logs, cleaning and restocking the lab, and practice good lab bench techniques to ensure high quality and consistent product. Roles and Responsibilities include but are not limited to: Manufacture high quality custom oligo containing products in a high throughput MFG lab according to established SOPs. Operation of robotic laboratory equipment and traditional lab equipment (bioanalyzers, centrifuges, sealers, thermocyclers, spectrometers, HPLCs, Next Gen Sequencing etc.) etc. | 5/6/2020 |
| 11330 | Twist Bioscience South San Francisco, CA Manufacturing Associate, NGS TE Production BS/AS in biology, chemistry, or biochemistry Exp: Not necessary for degree candidates |
The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. They will uphold standards as defined by the manufacturing process, work on continuous improvement and have good time management resulting in efficiency, and work in a safe manner. Roles and Responsibilities include but are not limited to: Manufacture high quality custom oligo containing products in a high throughput MFG lab according to established SOPs. etc. | 5/6/2020 |
| 11331 | Twist Bioscience South San Francisco, CA Manufacturing Associate, Oligo Production BS/AS in biology, chemistry, or biochemistry Exp: Not necessary for degree candidates |
The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. Roles and Responsibilities include but are not limited to: Manufacture high quality custom oligo containing products in a high throughput MFG lab according to established SOPs. etc. | 5/6/2020 |
| 11332 | Twist Bioscience South San Francisco, CA Manufacturing Associate, Reagents BS/AS in biology, chemistry, or biochemistry Exp: Not necessary for degree candidates |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate, Reagents is a great entry level role for anyone wanting lab experience as it gives the employee the opportunity to perform bench work, develop documentation skills, learn the inter-workings of a business and to build an understanding of biosynthesis and NGS. Roles and Responsibilities include but are not limited to: Perform aseptic techniques in a cleanroom environment to formulate buffers, antibiotic solutions and prepare culture media to meet manufacturing forecasts for gene production and NGS panels. etc. | 5/6/2020 |
| 11333 | Twist Bioscience South San Francisco, CA Manufacturing Associate, Vector Scale-Up BS/AS in biology, chemistry, or biochemistry Exp: Not necessary for degree candidates |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate, Vector Scale-Up will use standard Cellular and Molecular Biology techniques to produce high quality DNA through bacterial cell culture, DNA extraction and manipulation. The ideal candidate is a team player who can execute well established procedures in a safe and timely manner. Roles and Responsibilities include but are not limited to: Manufacture high quality custom oligo containing products in a high throughput MFG lab according to established SOPs. etc. | 5/6/2020 |
| 11334 | UCB Boston, MA Research Associate - Protein Purification BS/BA Exp: 1-2 year(s) |
Executing day to day laboratory activities with supervision to support Early Solutions research at UCB. The Research Associate (RA) will be trained in their basic responsibilities in their first year so that that they are able to consistently perform their duties with minimal supervision, and will be challenged with more advanced purifications as they advance in their position. Responsibilities in the Protein Purification Group Laboratory include but are not limited to the following: Execute all methods and techniques required to perform purification of soluble and secreted proteins utilizing the ӒKTA platform, SDS-PAGE, and TFF. etc. | 5/6/2020 |
| 11335 | Upsher-Smith Maple Grove, MN Quality Inspector I HS diploma or equivalent Exp: 0-2+ years |
The Quality Inspector I inspects and samples incoming raw materials manufactured outside of the company, packaging components and labeling materials, per sampling requirements. Completes all relevant SAP transactions to document inspection and sample consumption. Submits samples to laboratory. Inspects all labeling components for correctness against the approved proofmaster. (eg., text, barcodes and revision date). Applies appropriate stickers (e.g., RD, reject and hold) as necessary. Initiates data packets for incoming materials, if applicable. Receives laboratory samples from production by performing the appropriate SAP transactions. etc. | 5/6/2020 |
| 11336 | Veeva Philadelphia, PA Associate Consultant (Remote) BS/BA Exp: Not required |
You will be part of our Consultant Development Program working on project teams implementing Veeva’s cloud software applications. Participate in business process discovery workshops, gather requirements, configure the solution, help with testing and final deployment. Explain solutions to a variety of audiences and provide subject matter expertise on Veeva applications and technical design. This is a remote position. etc. | 5/6/2020 |
| 11337 | Veeva Columbus, OH QA Engineer BS in mathematics or computer science Exp: 0-5 year(s) |
Veeva Systems is looking for an energetic and enthusiastic Engineer to join our rapidly growing team. This is a hands-on position for delivering a quality SaaS product. As part of Veeva CRM Multi Channel software QA team, you will be given an opportunity to test a high quality product that was built from scratch. We are a fast-paced team who takes pride in building great software and making customers happy. What You'll Do: Design and implement test strategies. etc. | 5/6/2020 |
| 11338 | Veeva Toronto, ON QA Engineer - Safety BS in mathematics or computer science Exp: 1-4 year(s) |
Veeva Systems is looking for a QA Engineer that likes to figure out how things work and make sure they are working correctly. This is a hands-on position for delivering a quality SaaS product. You should want to be part of fast-paced team who takes pride in building great software and making customers happy. Come join us in building game-changing products for Pharmacovigilance (drug safety). What You’ll Do: Create testing-related documentation, including test plans, test cases/scripts, and bug reports assessing quality and associated risk. etc. | 5/6/2020 |
| 11339 | Veeva Pleasanton, CA Associate Automation Infrastructure Engineer unspecified Exp: 1-3 year(s) |
Do you want to be part of an engineering team that strives to build simple solutions to complex problems? Veeva is looking for a passionate engineer to work at our Pleasanton location for the Vault Automation Infrastructure & Tools team. This is a great opportunity to put your creativity and problem-solving skills to test. You would be working as part of a team that constantly strives to turn innovative ideas into reality using bleeding edge technology and a bouquet of programming languages. If you are a fresh graduate or someone who's recently started their career, this is a great opportunity for you to learn/ contribute and advance your career to the next level. etc. | 5/6/2020 |
| 11340 | Veeva Pleasanton, CA Associate QA Engineer BS/BA Exp: Not required |
Veeva QA Engineers are an integral part of our development team, who ensure Veeva products are quality SaaS products. They are curious and like to figure things out and make sure everything is working correctly before it reaches our customers. They enjoy breaking software to find ways to improve the product. Because they typically come from an engineering or applied science field, they are able to understand where bugs may come into the application and where to look for them. While developers typically work on one piece of the product, QA Engineers work on broader aspects of the product making sure all the pieces are working well together. They are good communicators who find the balance of maintaining a cooperative relationship with our developers, pushing back with tact and diplomacy, using good judgment and open to hearing various sides to an issue. etc. | 5/6/2020 |
| 11341 | Veeva Toronto, ON Associate Automation Engineer BS/BA in computer science or related Exp: Not required |
What You'll Do: Develop test cases in Java and Selenium in the Automation test framework. Contribute to the automation test framework and automation architecture. Create and improve testing related documentation including test plans, test cases, and automation scripts. Contribute to Devops activities including deployment, Continuous Integration / Continuous Deployment, infrastructure as code, Docker / containerization. etc. | 5/6/2020 |
| 11342 | Viant Brimfield, MA Machinist HS diploma or equivalent Exp: 6-12 months |
The primary purpose of this job is to set up, operate, and maintain CNC equipment to manufacture precision parts. Accountabilities & Responsibilities: Adheres to Viant’s Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. Operates and sets up CNC shop equipment with minimal assistance. Accountable for meeting cycle time and yield expectations. etc. | 5/6/2020 |
| 11343 | Viant Westfield, PA Machine Operator - Part Time HS diploma or equivalent Exp: Not necessary |
This position ensures that assigned machines/equipment produce product at or above department standards. Responsible to produce, assemble, inspect and pack all parts as per the work instructions for each assigned task or machine. Maintain all required paperwork and documentation to Good Manufacturing Practice (GMP) and ISO 13485 standards. Main Job Duties/Responsibilities: ATTENDANCE IS PARAMOUNT. All associates are required to report to work on time and when scheduled. Operate machines maintaining productivity, efficiency and product quality. etc. | 5/6/2020 |
| 11344 | Viant Grand Rapids, MI Manufacturing Operator 1 - ALL SHIFTS HS diploma or equivalent Exp: 6-12 months |
Under the direction of the area Supervisor, responsible for production work according to specifications and established policies, procedures, practices and standards. Main Job Duties/Responsibilities: Follows all Good Manufacturing Practices (GMP’s) and Standard Operating Procedures (SOP’s) as defined by Viant policies, practices and procedures to insure that FDA and ISO regulations and quality standards are met. Assembles components. May be required to operate packaging machine. Barsealing/Traysealing. Boxes products and applies labeling materials. etc. | 5/6/2020 |
| 11345 | Viant Indianapolis, IN Manufacturing Team Member - Deburr Department HS diploma or equivalent Exp: Not necessary |
The primary purpose of this role is to perform assembly and inspection operations over a range of products and processes. Will support both cyclical and non-cyclical work, independently preparing work to be accomplished by studying manufacturing process instructions and quality work instructions, gathering parts, tools, and materials as required. May train other team members in assembly operations. Job Description Details: Adheres to Viant Medical’s Core Beliefs, Behavioral Based Safety process and Quality Policy. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI’s) and Quality Work Instructions (QWI’s). Understands own tasks and how they relate to others in their team. Works under minimal Supervision. Will follow Standard Work where applicable. Understands overall production flow within their department. May perform significant non-cyclic work for the department. etc. | 5/6/2020 |
| 11346 | Veeva Toronto, ON QA Engineer - Andi BS in engineering, math, computer science or related Exp: 1-4 year(s) |
Veeva is looking for a QA Engineer that likes to figure out how things work and make sure they are working correctly. This is a hands-on position for delivering a quality SaaS based product. You should want to be part of fast-paced team who takes pride in building great software and making customers successful. Come join us in building a game-changing product to help deliver real-time insights and suggestions via Artificial Intelligence. What You’ll Do: Ensure that all assigned project deliverables meet quality objectives in functionality, performance, stability, security, accessibility and data quality. etc. | 5/6/2020 |
| 11347 | ThermoFisher Scientific High Point, NC Machine Operator (Encapsulation) - (Nights C shift) HS diploma or equivalent Exp: 1 year |
Responsibilities: Reads job specifications from the Batch Production Record to determine machine adjustments and material requirements. Observes machine operation. Makes adjustments as needed. Takes samples of product and performs in process testing. Performs all checks as required and documents activities. Is responsible for maintaining all required documentation in accordance with the Work Instructions of Patheon / Thermo Fisher Scientific. Assists Set-Up person to set up machine, empty basket and clean and prepare machine for changeover. Also assists with the actual changeover. etc. | 5/6/2020 |
| 11348 | ThermoFisher Scientific High Point, NC Printing Associate HS diploma or equivalent Exp: 1+ year(s) |
What will you do? Set up printing equipment by installing carrier bars, brushes, stripper plate, blow off tubes, gravure roll, rubber roll, ink pan and doctor blade. Set up the vision equipment (install proper belt/color, load appropriate recipe, install proper target, train the cameras, verify background) and trouble-shoot as needed. Work safely to prevent on the job accidents and injuries by observing moving equipment and adhering to all job safety procedures such as wearing PPE. Document work performed by completing forms and logs accurately. etc. | 5/6/2020 |
| 11349 | ThermoFisher Scientific High Point, NC Medicine Associate HS diploma or equivalent Exp: 1 year |
Manufacture a quality fill material for use in encapsulation utilizing multiple types of equipment and processes to accomplish this. Works safely to prevent on the job accidents and injuries by observing moving equipment; adhering to all job safety procedures; attending plant safety training; shift safety meetings; adhering to lockout/tag out procedures; wearing appropriate personal protective equipment (PPE) such as captive clothing, steel-toe shoes, respirators, and additional gowning if necessary. Able to be adaptable to a dynamic work environment. At batch initiation and during batch processing performs the following: check lot numbers; check weights; check raw material lot numbers; check part numbers; ensure expiration dates are within acceptable range by comparing the various print-outs and labels with the batch processing record (BPR). Follows BPR instructions as guided. etc. | 5/6/2020 |
| 11350 | ThermoFisher Scientific Middletown, VA Manufacturing Operator (2nd Shift Fill/Label/Pack) HS diploma or equivalent Exp: 1 year |
Manufacturing Operators work alone or with other operators to perform filling and/or packaging of products by complying with GMP (Good Manufacturing Practices), ISO 13485 guidelines and company Standard Operating Procedures (SOPs). What will you do? Perform duties on production line to prepare, assemble and pack products as required. Must be able to complete and understand production paper work with minimal to no errors, up to and including product reconciliation, label reconciliation, labor sheets, product fill checks, torque checks, etc. Cleans and sanitizes work areas, machines, glassware or equipment as needed or directed, if required in work area. etc. | 5/6/2020 |
| 11351 | ThermoFisher Scientific Durham, NC Proposals Specialist BS/BA in science or business Exp: 0-2+ years |
The Associate Drug Product Commercial Proposal Specialist will take customer provided technical information along with reasonable assumptions and estimate the cost and pricing for late phase transfer programs as well as ongoing commercial supply for pharmaceutical products. This position will then write the related bid proposals that will be issued to the customer through the sales team. This position will support the sales efforts related to the opportunities that they quote on as well as manage the relevant quote records in Salesforce.com. etc. | 5/6/2020 |
| 11352 | ThermoFisher Scientific Mississauga, ON Proposals Specialist BS/BA in science or business Exp: 0-2+ years |
The Associate Drug Product Commercial Proposal Specialist will take customer provided technical information along with reasonable assumptions and estimate the cost and pricing for late phase transfer programs as well as ongoing commercial supply for pharmaceutical products. This position will then write the related bid proposals that will be issued to the customer through the sales team. This position will support the sales efforts related to the opportunities that they quote on as well as manage the relevant quote records in Salesforce.com. etc. | 5/6/2020 |
| 11353 | Unity Biotechnology South San Francisco, CA Research Associate 1/2, in vivo Pharmacology MS in biology, physiology, bioengineering, or related Exp: 1-2 year(s) |
The candidate should be creative and have both a passion for biology and an interest in using animal models to study human disease. The position requires a self-motivated individual seeking a hands-on, lab-based role using in vivo animal models and in vitro methodologies to contribute to specific project goals as part of a dynamic team. The duties of the job include animal handling/dosing, experimental design and execution, analysis/interpretation of data, downstream sample generation/ samples processing, and presentation (verbal/written) of findings at team meetings. etc. | 5/6/2020 |
| 11354 | Unity Biotechnology South San Francisco, CA Research Associate in-vivo Pharmacology MS in cellular biology, physiology, or related Exp: Not necessary for MS candidates |
We are seeking to hire a research associate to join the in vivo pharmacology team at Unity. This position will afford the successful individual an opportunity to discover clinical candidates for an emerging and exciting biology and the potential to translate our science into a pipeline of differentiated medicines. The ideal candidate will be enthusiastic, innovative, and possess a diverse technical skill set having worked on a variety of in vivo models. At Unity, this experience will be applied towards the successful discovery of novel small molecules for the selective elimination of senescent cells in diseases associated with aging. etc. | 5/6/2020 |
| 11355 | Baxter Marion, NC Technician, Formulation HS Diploma/GED Exp: 1 year in manufacturing |
Perform and document scheduled cleaning activities which include using a ladder and safety harness to climb into mixing tanks in order to clean the inside of the vessel. Inspect, clean and re-palletize raw materials received from the warehouse. Following standardized formulas, apportion, measure, weigh, label and stage raw materials. | 5/3/2020 |
| 11356 | Baxter Marion, NC Quality Lab Assoc I BS in microbiology or biological sciences Exp: 0-2 years |
Conduct microbiological analyses on raw materials, in-process and finished products. Collect samples related to Environmental Monitoring program at Baxter manufacturing area. Use laboratory instrumentation and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of microbiological principles. | 5/3/2020 |
| 11357 | Baxter Round Lake, IL Manufactuirng Supervisor I, 2nd Shift BS/BA Exp: 1 year experience |
The supervisor position is responsible for implementing and supervising daily activities in a specific production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (GMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply.May monitor and control labor. | 5/3/2020 |
| 11358 | Baxter Round Lake, IL Quality Lab Associate I BS in microbiology or biological sciences Exp: 0-2 years |
Conduct biological, chemical and physical analyses on pharmaceutical products (biologic and drugs) and medical devices through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs Conduct critical biological, physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities | 5/3/2020 |
| 11359 | Baxter Round Lake, IL Engineer II BS in engineering Exp: 1-3 years |
With supervision, lead projects within Baxter’s change control management process, from initiation through closure. Change Owners assign and prepare impact assessments, develop change plans, write and execute engineering studies, while working closely with manufacturing plants, quality, regulatory, purchasing, and various scientific/technical groups. | 5/3/2020 |
| 11360 | Baxter Round Lake, IL Quality Lab Associate I BS in microbiology or biological sciences Exp: 0-2 years |
Conduct biological, chemical and physical analyses on pharmaceutical products (biologic and drugs) and medical devices through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs Conduct critical biological, physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities | 5/3/2020 |
| 11361 | Baxter Round Lake, IL Quality Lab Associate I BS in microbiology or biological sciences Exp: 0-2 years |
Conduct biological, chemical and physical analyses on pharmaceutical products (biologic and drugs) and medical devices through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs Conduct critical biological, physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities | 5/3/2020 |
| 11362 | BD Sumter, SC Micro Lab Technician HS Diploma/GED Exp: 0-1 years in clean room experience |
Performs testing that assures the sterility of BD product, in addition performs environmental monitoring of manufacturing areas to ensure that product integrity. Familiarity with Microbiology techniques, equipment and good laboratory practices, including a working in clean room atmosphere is preferred. Duties will include collection test samples, media preparation, verification/calibration of equipment, upkeep of various laboratory databases, routine housekeeping, and providing support to special projects. | 5/3/2020 |
| 11363 | BD Sumter, SC Validation Technician HS Diploma/GED, Associates Preferred Exp: 1 year in quality |
Support the Compliance group by performing various tests, collecting data and being the QA floor representative relating to validation / process characterization projects. Reports directly to a Quality Manager. Conduct experiments and collect data for use in analysis of quality cost, process capability, etc. Perform measurements using precision equipment with accuracy to .0001” | 5/3/2020 |
| 11364 | BD Columbus, NE Product Line Coordinator BS/BA in business admin, management, industrial tech Exp: 1-3 years in manufacturing |
The Product Line Coordinator is responsible for all production management and supervisory activities and to support the Unit Manager in setting and achieving overall business objectives for all product lines including compliance to cost, quality, safety, human resource and regulatory plans and requirements. Administer plant policies (safety, attendance, disciplinary actions). Responsible for training of new employees including new operator orientation, ITR's, and appropriate counseling/coaching. | 5/3/2020 |
| 11365 | BD Sandy, UT Process Specialist HS Diploma/GED Exp: 1-2 years in manufacturing |
The Process Specialist Operates high speed automated manufacturing equipment in the Surgical Scrub department. Operates high speed automated manufacturing equipment. Ensures that correct doses of the active ingredients are dispersed. Responsible for readying production equipment and materials during product changeovers. Responsible for set-up of work stations and bringing in materials for production order. | 5/3/2020 |
| 11366 | BD Columbus, NE Small Gauge Packroom Operator - B shift HS Diploma/GED Exp: 0 years required |
Run auto inspection machines and assist in Changeovers, and trouble-shooting machines in the Cannula Department. Perform 100% Inspect Qc checks, and check material into SAP . Support the activities of the department as necessary to meet objectives. The nature of these jobs requires flexibility and adaptability as condition change. Assist QC Manufacturing Representative and /or QC Technician in performing machine and process capability studies, etc. | 5/3/2020 |
| 11367 | BD Baltimore, MD QM Associate Scientist BS/BA in biological sciences Exp: 1-2 years |
Responsible for Microbiology Quality Control testing in peptone manufacturing, raw material products, Tissue Culture Testing, Dyes & Stains testing and Final DCM testing as required. The QM Associate Scientist is required to perform testing of various Microorganisms in a Biosafety Level II and TB Laboratory with strict adherence to safety policies. | 5/3/2020 |
| 11368 | Beam Therapeutics Cambridge, MA Research Associate - Analytical Services Team MS in biological/chemical sciences, or engineering Exp: 0-3 years in pharma |
Working closely with scientists in our development group, this candidate will take a lead role in optimizing, running and interpreting data from a variety of assays to characterize our lead candidate materials. As part of a cross-functional team, optimize and execute a variety of HPLC/UPLC/LCMS methods to assess the purity and integrity of proteins and nucleic acid molecules (natural and synthetic, short and long, RNA and DNA); | 5/3/2020 |
| 11369 | Beam Therapeutics Cambridge, MA Research Associate, In Vivo Immuno-Oncology BS/BA or MS in biotechnology/pharma Exp: 1-2 years |
The candidate will be responsible for conducting preclinical animal studies to support the development of ex-vivo cellular therapies. They will also perform downstream in-vitro assays. Design, plan, and execute in-vivo studies in immunodeficient mice for immuno-oncology indications. Perform routing procedures and injections (SC, IP, IV, PO) in mice, monitor animal health, measurements, and sample harvest for multiple tissues. | 5/3/2020 |
| 11370 | Beckman Coulter Miami , FL Medical Technologist Customer Technical Support Associates in biological/chemical/physical science or engineering Exp: 1-2 years in customer service |
Provide general technical consulting to customers and company staff distinguishing among hardware, reagent and software issues in order to resolve or dispatch the appropriate resource at minimum company expense. Through telephone and electronic (i.e. email) technology provide resolutions on Hardware, Software, Assay and Training related calls from existing customer base. | 5/3/2020 |
| 11371 | Beckman Coulter Brea , CA Facilities & Operations Technician AA degree Exp: 1+ years |
Enables business to meet and exceed operational goals by completing timely preventative maintenance duties to maintain safe, stimulating and socially responsible building environment. Supports a team culture of continuous improvement for the office and manufacturing environment that ensures safety, efficiency, hygiene, and sustainability. | 5/3/2020 |
| 11372 | Bayer Indianola, PA Assembler I - 2nd Shift 2:00pm - 10:20pm HS Diploma/GED Exp: 0-1 years working |
Assemble and package various products; Perform rework and inspection on the product;Be aware of quality standards and ability to identify defects in products; | 5/3/2020 |
| 11373 | Bayer Pittsburgh, PA Machine Operator I - D2 6am-6pm HS Diploma/GED, Associates Preferred Exp: 0-2 years |
Understand the potential hazards and safe equipment operating practices in a manufacturing environment; Understand the quality systems and guidelines that impact areas of responsibility including component specifications, equipment operating parameters, data collection and cleanliness requirements; Ensure all potential equipment deficiencies and component defects are properly identified throughout areas of responsibility to ensure adherence to quality guidelines; | 5/3/2020 |
| 11374 | Bayer Muscatine, IA Packaging Tech HS Diploma/GED, Associates Preferred Exp: 1 year in electrical/mechanical work |
Operate, maintain, and repair packaging equipment as well as troubleshoot problems associated with equipment, process, or systems; Perform mechanical maintenance and preventative maintenance on packaging equipment; Complete equipment repair notifications and work directly with Maintenance Technicians on any repairs requiring their assistance; | 5/3/2020 |
| 11375 | Bayer Marshall , MO Seed Technician HS Diploma/GED Exp: 0-2 years |
Operate equipment in the production sites and leveraging real time data to maximize existing procedures; Perform preventive maintenance and inspections; troubleshooting problems associated with equipment, processes and systems as needed; Support areas across the plant in driving the adoption of continuous improvement practices and programs (5S, Lean, Six Sigma) conducive to an organized and clean work environment; | 5/3/2020 |
| 11376 | Beckman Coulter Minneapolis, MN Human Resources Representative I BS/BA in human resources Exp: 0-2 years |
The selected individual will provide counsel and assistance to broad employee populations, including front-line associates and senior managers. In support of these client groups, this role will be responsible for end-to-end human resources work including recruitment, training facilitation, employee relations, management consulting, metrics reviews, and all applicable annual processes. | 5/3/2020 |
| 11377 | Beckman Coulter Chatsworth, CA Field Service Engineer - Chemistry/Automation: Northern LA Associates Exp: 1-3 years |
Under minimal supervision, serve as lead to assigned customers; complete troubleshooting, installation, validation, maintenance, and service repair needs on designated equipment. May assist and/or train newer Field Engineers. Provide excellent and efficient service to Beckman Coulter’s customers, along with technical training on products | 5/3/2020 |
| 11378 | Beckman Coulter Chaska, MN Software Engineer I - Diagnostic Instrument BS/BA in computer science, biomedical engineering, or related Exp: 0 years required |
As part of the software development team, you’ll work with a variety of technologies to bring new products to market. We develop product software with primarily a C#/.NET windows-based technology stack. As an R&D software engineer, you could be writing code to control mechanical systems, design UIs, and interact with databases and web services. | 5/3/2020 |
| 11379 | Avexis San Diego, CA Quality Control Analyst (In vitro Bioassay) BS/BA in biochemistry or related Exp: 1 year in GMP lab |
The individual should have enriched experience in culturing transformed and primary cells and banking cells. In addition, experience in testing samples using qualified cell-based assays (e.g. virus infection assays and proliferation assays) is desired. Additional responsibilities include adherence to all GMP requirements, a basic understanding of FDA/EMEA regulations, effective interactions/communication with Quality management and support of investigations. The QC Analyst may also support identification and implementation of corrective and preventive actions. | 5/2/2020 |
| 11380 | Avid Bioservices Tustin, CA Biomanufacturing Technician (Buffer/Media Support) AA or HS Diploma Exp: 0-1 year in life science industry |
The Manufacturing Technician provides support for: Production Operations and multiple aspects of cGMP contract cell culture manufacturing in strict compliance with cGMP, under Standard Operating Procedures in a multi-product manufacturing facility, including, but not limited to: production, documentation, writing reports, requesting and purchasing materials, and scheduling equipment services and calibrations | 5/2/2020 |
| 11381 | Avid Bioservices Tustin, CA Biomanufacturing Associate/Technician (Downstream Purification) BS/BA in life sciences Exp: 0-1 years (technicial level) |
As a Biotech Manufacturing Associate / Technician, you play an integral role in ensuring the on-time delivery of quality biopharmaceutical products. You get to participate in a variety of tasks including purification of biologics, keeping up-to-date GMP documentation, writing reports, ordering materials, and scheduling equipment services. | 5/2/2020 |
| 11382 | Avid Bioservices Tustin, CA Shipping Clerk, Supply Chain (Entry-Level) AA or HS Diploma Exp: 0-2 years in shipping |
Schedule shipments with carrier including waybill and commercial invoice if needed. Complete sample packaging and shipping duties. Organize all shipping supplies in an easy to locate and count fashion. Coordinate the efficient movement of samples with QC, Manufacturing and other departments under cGMP standards | 5/2/2020 |
| 11383 | Avidity La Jolla, CA Research Associate I/II, DMPK BS or MS in bioengineering/chemistry/biology Exp: 1-3 years previous lab experience |
We are seeking a Research Associate to join the Drug Metabolism & Pharmacokinetics (DMPK) team at Avidity Biosciences in La Jolla, CA. This position will require hands-on lab work with responsibility for processing and analyzing animal blood and tissues, RNA isolation, quantitative RT-PCR, ELISA, Nanostring, mammalian cell culture, western blot, chromatography (RP-HPLC, SAX, SEC, etc), and pharmacokinetic analysis. | 5/2/2020 |
| 11384 | Avomeen Ann Arbor, MI Analytical Chemist/Scientist BS/MS in chemistry Exp: 0-5 years |
Learn techniques spanning across the entire spectrum of analytical chemistry from wet chemistry to HPLC, NMR, Mass Spectrometry, FTIR, GC and GC-MS. Perform testing using a variety of technologies including HPLC, LC-MS, GC, GC/MS, Microscopy, FTIR and UV. Execute projects in support of client needs including product deformulation and product development, failure analysis and problem solving, impurity identification, extractable and leachable studies, and structural characterization | 5/2/2020 |
| 11385 | Axonics Irvine, CA QAD Administrator Associates or technical certificate Exp: 1 year in enterprise resource planning |
Translates operations to streamline workflow processes within the ERP application. Configures, administers, upgrades and maintains the company's ERP. Optimization and streamline business processes within QAD and other IT areas as needed. Monitors system performance and usage to maintain security and reliability, coordinates new software releases, fixes, and upgrades with technical team and users. | 5/2/2020 |
| 11386 | Axsome New York, NY Clinical Trials Assistant BS in biological/physical sciences or nursing Exp: 1 year in clinical department |
The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. Assist with all phases of clinical study activities (feasibility, start-up, maintenance, and close-out). | 5/2/2020 |
| 11387 | Azzur Group Waltham, MA Validation Engineer (Consultant) BS in engineering/sciences Exp: 1-7 years in manufacturing environment, regulated |
Development and editing of technical documentation including: Standard Operating Procedures, User Requirements and Design Specifications, Commissioning and Qualification Protocols. Development of project plans, as appropriate. Execution of validation test procedures | 5/2/2020 |
| 11388 | Azzur Group Herndon, VA Cloud Automation Engineer BS/BA in computer sciences or related Exp: 1-2 years experience in C/C++/Java/etc. |
Support services before they go live through the process of developing automation, developing security frameworks, and planning continuous delivery cycles. Engage in and improve the complete lifecycle of services inception and design, through deployment, operation, and refinement.Maintain services that are live by helping to measure and monitor availability, security, and overall system health. | 5/2/2020 |
| 11389 | Bachem Torrance, CA Production Chemist I BS in chemistry or related Exp: 1-3 years work experience |
The Chemist (Chem1) function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. Perform synthesis process including solution phase and solid phase peptide synthesis, peptide resin cleavage, resin cleavage with HF or other chemical cocktails. Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities | 5/2/2020 |
| 11390 | Bachem Torrance, CA Research & Development Chemist I BS/BA in chemistry/biochemistry/bioengineering Exp: 1-3 years, MS: 0 years |
The R&D Chemist I position will be responsible for synthesis and cleavage of GMP grade peptides under GMP regulations. This work will encompass small/medium scale solid-phase peptide synthesis and TFA cleavage to generate crude peptide products for further purification processing. Perform solid-phase peptide synthesis (SPPS) and cleavage/crude peptide isolation steps with direction from Supervisor | 5/2/2020 |
| 11391 | Bachem Torrance, CA Metrology Technician HS Diploma/GED Exp: 11-2 years in instrumentation/electrical systems |
The Facilities Metrology Technician, under close supervision, performs routine calibration duties such as: tests, calibrations, repairing electrical, mechanical, electro-mechanical, and electronic measuring, recording, and indicating instruments and equipment for conformance to established standards. Thisindividual will also be responsible for all related projects and services related to the facilities equipment and their timely completion while adhering to standard practices. | 5/2/2020 |
| 11392 | Bachem Torrance, CA Production Technician Associates in chemistry or sciences Exp: 0-2 years |
The Production Technician I performs an integral role as part of the Production team at Bachem. This role is responsible for contributing to the safe and economic manufacture of active pharmaceutical ingredient (API) products, such as peptide or related bioorganic compounds, as a member of a production team. As a Production Technician I, you will be producing APIs from gram to multiple kg scale. | 5/2/2020 |
| 11393 | Bachem Torrance, CA Research & Development Chemist II MS in chemistry/biochemistry Exp: 1-3 years |
Perform preparative and analytical reversed-phase high performance liquid chromatography (HPLC) and isolation operations with direction from supervisor. Follow written procedures such as Standard Operating Procedures (SOP) and Batch Production Records (BPR). Comply with SOP’s in all aspects of the work and follow GMP regulations. With appropriate training, become well-versed in operation of specific chromatography platforms used in the GMP Manufacturing Group | 5/2/2020 |
| 11394 | Bachem Torrance, CA Chemist I BS in chemistry or related Exp: 1-3 years |
Perform synthesis process including solution phase and solid phase peptide synthesis, peptide resin cleavage, resin cleavage with HF or other chemical cocktails. Perform purification process by chromatography, crystallization and other techniques, and in-process test method. Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities. | 5/2/2020 |
| 11395 | Bachem Torrance, CA QA Specialist I BS/BA in sciences or related Exp: 1-2 years in GMP/Manufacturing |
The Quality Assurance Specialist I fulfills a critical role for Quality Assurance. This individual will conduct real time batch record review, perform internal audits, contribute to GMP system improvements, write technical documents, and review GMP documentation and reports. This individual must also provide GMP and related training. | 5/2/2020 |
| 11396 | BardyDx Houston, TX Holter Analysis Technician HS Diploma/GED or Associates Exp: 1-3 years as telemetry/monitor tech |
This position requires PC proficiency, excellent written and verbal communication skills, and meticulous attention to detail. Process, analyze, interpret, and edit ECG data for clinical accuracy and completeness. Evaluate and effectively communicate ECG abnormalities to lead technicians and/or physicians and physician staff based on established notification criteria. Maintain CCT or CRAT proficiency requirements. (CCT or CRAT certification must be obtained within 90-days of date of hire). | 5/2/2020 |
| 11397 | Inotiv Gaithersburg, MD Pathology Technician I BS/BA in biological sciences Exp: 1 year lab experience |
Learns how to review study protocol and ensure study tasks and data for pre-clinical research studies are conducted in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. Learns to serve as head technician for basic studies and to perform protocol review in preparation for PI meeting attendance. Position requires the ability to manage multiple studies within scope of expertise. | 5/2/2020 |
| 11398 | Inotiv Fort Collins, CO Administrative & Accounting Assistant HS Diploma/GED Exp: 1-2 years in business office setting |
notiv in Fort Collins is looking for a part time Receptionist/Administrative Assistant. This is a 12-20 hour a week position, Monday – Friday with a start time of 7:00 AM. The successful candidate must be dependable, polite, flexible and skillful in handling many different administrative tasks for a small medical research facility. | 5/2/2020 |
| 11399 | Bausch Health Companies Wilmington, MA Electro-Mechanical Technician Associates in mechanical/electrical field Exp: 1-2 years |
Provide electro-mechanical maintenance support to all existing manufacturing equipment and ancillary processes, ensuring continuous operation with minimal downtime. Performs required maintenance, troubleshooting, and repair of production equipment to resolve mechanical and electrical issues. Other aspects of the position include project work as well as routine maintenance support. | 5/2/2020 |
| 11400 | Avexis Longmont, CA Quality Control Technician (Microbiology) BS/BA in microbiology or related Exp: 0-1 years |
This position will work with the Quality Control team in supporting our efforts in this exciting new area of gene therapy. This position will be responsible for environmental monitoring, product and raw material testing, and other general QC microbiology sampling and testing processes. Perform environmental and utilities monitoring in clean rooms and subsequent analyses. | 5/2/2020 |
| 11401 | Avexis Libertyville, IL Training Associate BS/BA Exp: 1-3 years in training |
The Training department is responsible for developing the skills and knowledge of site employees, allowing development within their current role, as well as enhancing careers within AveXis. The Training Associate is responsible for the day-to-day operation of the Learning Management System (LMS), monitoring and reporting compliance to the program, and assisting with the identification and development of training content. | 5/2/2020 |
| 11402 | Avexis Libertyville, IL Quality Control Technician (Microbiology-Day Shift) BS/BA in microbiology or related Exp: 0-2 years |
This position will work with the Quality Control team in supporting our efforts in this exciting new area of gene therapy. This position will be responsible for environmental monitoring, product and raw material testing, and other general QC microbiology sampling and testing processes. Perform environmental and utilities monitoring in clean rooms and subsequent analyses. | 5/2/2020 |
| 11403 | Avexis Durham, NC Quality Control Investigations Specialist BS/BA Exp: 1-3 years in quality |
As part of the Manufacturing organization, the Quality Control (QC) Investigations Specialist will be responsible for the investigation and completion of laboratory investigations and non-conformances aimed at identification of root cause, assessing potential impact and implementation of corrective and preventive actions. The QC Investigations Specialist will help determine the validity of data, and determination of out of specification results. | 5/2/2020 |
| 11404 | Azzur Group Waltham, MA Operations Engineer I BS/BA in sciences Exp: 1-2 years in similar role |
Identifying and executing project actions to improve the Inventory Control System or the Computerized Maintenance Management System used to support Facility operations. Support the execution of equipment qualification and commissioning studies for shipping, facility utilities and equipment used in client process operations and in facility operations. Execute protocols and help resolve protocol deviations/discrepancies, analyze study data and write summary reports. | 5/2/2020 |
| 11405 | Serepta Therapeutics Cambridge, MA Specialist I, Patient Affairs BS/BA Exp: 1-3 year(s) |
The Operations Specialist I focus primarily on performing the day-to-day operations within the Patient Affairs team and streamlining Patient Affairs’ processes within our department, in addition to how we work with our internal, cross-functional partners. This role can improve the overall function of our department while also gaining exposure (and ultimately helping to drive the execution) of work across the team to partner with the patient/caregiver community externally and internally drive patient voice across Sarepta’s global sites. This role works primarily with Patient Affairs, in addition to policy, legal & compliance, marketing, corporate communications, information technology (IT), and regulatory. etc. | 4/29/2020 |
| 11406 | Serepta Therapeutics Dublin, OH Research Associate I, Histology BS in chemistry or a physical or biological science Exp: 1 year |
The Research Associate, Histology provides laboratory support of day-to-day GCLP/GLP testing on muscle/nerve and other tissue types using complex histology methods in accordance with the requirements of approved protocols. The RA has strong histology laboratory expertise and utilizes this experience to train others, maintain records of experiments, assist in analyzing data, and prepare laboratory reports. The RA participates in development, GCLP/GLP qualification, and validation of histology related assays to support clinical trials and clinical development decision-making. etc. | 4/29/2020 |
| 11407 | Serepta Therapeutics Durham, NC Research Associate I BS in biochemistry, immunology, bioengineering or related Exp: 1-3 year(s) |
The Research Associate I provides laboratory support, performs experiments and collects data on in vitro, ex vivo, and/or in vivo studies to investigate the effects of CRISPR-based gene editing on gene and protein expression, tissue pathology, and disease phenotype in animal models of neuromuscular disorders. The RA participates in development, GCLP/GLP qualification, and validation to support preclinical development, clinical trials and clinical development decision-making. | 4/29/2020 |
| 11408 | Serepta Therapeutics Burlington, MA IT Support Specialist I HS diploma/BS/BA Exp: 1-3 year(s) |
Level I Specialist primary duties include Tier 1 technical support, including software/hardware installation, troubleshooting, hardware break/fix, VoIP phone support and asset management. Primary Responsibilities Include: Provide Tier 1 technical assistance for computer hardware, software systems, and printers/copiers. Respond to inquiries via email, phone, walk-up or ticketing system. etc. | 4/29/2020 |
| 11409 | Serepta Therapeutics Andover, MA Associate I, Quality Control BS in chemistry or related Exp: 1-2 year(s) |
This individual will support quality control activities conducted both internally and at the Contract Test Laboratories (CTLs). The individual will be responsible for generating and reviewing release data, writing technical reports, and supporting analytical method validation and qualification activities conducted internally, as well as supporting the above tasks at the CTLs as needed. This individual will assist in transferring assays to and from domestic and overseas vendors and monitoring, compiling and reviewing data. The individual will also assist in managing laboratory investigations, quality events, data trending, review of quality documents originated at the testing laboratories as well as internally at Sarepta. etc. | 4/29/2020 |
| 11410 | Sedia Portland, OR QC Technician HS diploma/AS/AA Exp: 1-3 year(s) |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. Demonstrates a high level of independent judgment and discretion in the timely identification, investigation and resolution of events impacting the Quality of products and processes. etc. | 4/29/2020 |
| 11411 | Sedia Portland, OR Manufacturing Technician HS diploma/AS/AA Exp: 1+ year(s) |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. The Manufacturing Technician will adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance. etc. | 4/29/2020 |
| 11412 | Sekisui Charlottetown, PE Associate Scientist BS Exp: 0-2 years |
The Associate Scientist will be responsible for designing, executing and interpreting experiments and analytical procedures under general supervision. Initiates, directs and executes pre-clinical scientific research and/or development strategies in research and/or development. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems. Plans and executes laboratory research. Maintains broad knowledge of state-of-the-art principles and theories. May participate in development of patent applications. Interfaces with various departments. etc. | 4/29/2020 |
| 11413 | Sekisui San Diego, CA Maintenance Technician II HS diploma/AS/AA Exp: 1-2 year(s) |
The Maintenance Technician II performs preventative and/or corrective maintenance for all manufacturing and facility equipment according to the specifications and procedures. Executes electrical and mechanical troubleshooting to determine problems in non-functioning equipment used in the manufacturing process. Diagnoses, adjusts, repairs, tears-down and re-assembles equipment. Uses test and diagnostic equipment to perform inspections. Completes maintenance records in accordance with Good Manufacturing Practices. Coordinates with vendors to ensure work is conducted in a timely and safe manner. etc. | 4/29/2020 |
| 11414 | Sekisui Kansas City, KS Research Assistant BS in a biological and chemical science Exp: 1+ year(s) |
SEKISUI XenoTech, LLC is currently hiring for an entry level Research Assistant to the Enzyme Incubations Team within the Program Execution department. The Research Assistant assists with routine laboratory functions including diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintains inventory of supplies, and various other responsibilities. Essential duties and responsibilities include, but are not limited to the following: Design and conduct routine experiments. Maintains laboratories and equipment. etc. | 4/29/2020 |
| 11415 | Seracare Cumberland Foreside, ME Manufacturing Chemist I BS in biology, chemistry, or medical technology Exp: 0+ years |
The Manufacturing Chemist I prepares reagents, buffers, stocks and other solutions relying on established procedures within a controlled production environment. This role also performs the analysis and interpretation of test results within pre-established guidelines. The Manufacturing Chemist at this level is familiar with: Basic laboratory equipment and techniques. etc. | 4/29/2020 |
| 11416 | SomaLogic Boulder, CO Laboratory Technician I/II AS in a physical, biological, or medical science Exp: 6 months |
SomaLogic is a rapidly growing privately owned biomedical science company that has developed a revolutionary proteomics technology capable of measuring thousands of proteins in a single sample. We are a dedicated team of science-based colleagues working to build new tools based on our technology that will change the way life science research is done and healthcare is delivered. The Laboratory Technician I, II, or Associate I position in our U.S. Regulated Clinical Laboratory, located in Boulder, CO. The primary role of this position is to perform routine testing of patient samples using robotic liquid handling systems. etc. | 4/29/2020 |
| 11417 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I BS in the life sciences Exp: 1+ year(s) |
We are currently seeking a Manufacturing Associate who will be responsible for performing and supporting Downstream manufacturing tasks. Including but not limited to: Maintain GMP compliance in clean rooms. Responsible for Downstream GMP processing activities: buffer preparation, antibody purification, and drug substance formulation. Support material inventory control for downstream activities. etc. | 4/29/2020 |
| 11418 | SteriPharma Syracuse, NY Production Maintenance Technician, 2nd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. How you make a difference . . . you will . . . Performs maintenance work, to include equipment repair and preventative maintenance work as required or assigned. Performs the repair and maintenance of APA area floors and walls. Completes work orders and projects as assigned, supporting each team member as directed. etc. | 4/29/2020 |
| 11419 | Steris Reno, NV Field Service Technician AS/BS in electronics, mechanics, or related Exp: 1+ year(s) |
At STERIS, our Field Service Technicians act as the face of our company by ensuring top-notch service for our customers. In this field-based, customer-facing role, you will travel to hospital and surgical facilities to maintain, troubleshoot, service, and provide calibration and installation support for steam sterilizers, medical equipment washers and other STERIS products as needed. In addition, you will be responsible for building positive relationships with customers and colleagues, as well as completing necessary administrative tasks. etc. | 4/29/2020 |
| 11420 | Steris Minneapolis, MN Installation Technician AS/AA in electronics, mechanical, or related Exp: 1+ year(s) |
STERIS’ Installation Technicians act as the face of STERIS by achieving One of a Kind Service for our Customers. The Installation Technician is a field-based, Customer-facing role that primarily travels to Customer sites (medical facilities) to install Operating Room and Sterile Processing Department equipment. They provide complete equipment installation in accordance with plans and specifications including scheduling, delivery, installation, check-out, and final inspection of equipment. Installation Technicians are also responsible for building positive relationships with Customers and peers, as well as completing necessary administrative tasks. etc. | 4/29/2020 |
| 11421 | Steris Toronto, ON Field Service Technician AS/BS in electronics, mechanics, or related Exp: 1+ year(s) |
At STERIS, our Field Service Technicians act as the face of our company by ensuring top-notch service for our customers. In this field-based, customer-facing role, you will travel to hospital and surgical facilities to maintain, troubleshoot, service, and provide calibration and installation support for steam sterilizers, medical equipment washers and other STERIS products as needed. In addition, you will be responsible for building positive relationships with customers and colleagues, as well as completing necessary administrative tasks. etc. | 4/29/2020 |
| 11422 | Steris Richmond, VA Technician I HS diploma or equivalent Exp: 1-3 months |
The primary role of the Repair Technician is to perform repairs on medical instrumentation. Technicians will be trained to become familiar with various types of surgical instruments and understand how to best maintain and repair them. Repairs are completed on a repair truck onsite at a hospital or surgery center. In addition to repair work, Technicians may work with a team including Sales Representatives and RCs (Repair Consultants/Managers) to identify and capitalize on revenue opportunities. Travel requirements may vary by location. etc. | 4/29/2020 |
| 11423 | Steris Clifton, NJ Installation Technician AS/BS in electronics, mechanics, or related Exp: 1+ year(s) |
STERIS’ Installation Technicians act as the face of STERIS by achieving One of a Kind Service for our Customers. The Installation Technician is a field-based, Customer-facing role that primarily travels to Customer sites (medical facilities) to install Operating Room and Sterile Processing Department equipment. They provide complete equipment installation in accordance with plans and specifications including scheduling, delivery, installation, check-out, and final inspection of equipment. Installation Technicians are also responsible for building positive relationships with Customers and peers, as well as completing necessary administrative tasks. etc. | 4/29/2020 |
| 11424 | Stryker Casper, WY JR Sales Associate BS/BA Exp: 1+ year(s) |
What you will do: Increasing Joint Replacement sales through assisting the sales teams and building own accounts by means of working with existing customers as well as identify new customers in order to grow their territory. Communicating with current and new Joint Replacement customer accounts regarding a variety of topics including product updates, changes to product portfolio and educational programs. etc. | 4/29/2020 |
| 11425 | Stryker Davie, FL Quality Assurance Technician HS diploma Exp: 1-2 year(s) |
Job Description: Maintain certification to inspect a minimum of one business units products and Incoming Inspection equipment. Perform incoming inspection on components and Electro/mechanical products per company/regulatory specifications. Work from engineering schematics or blueprints to perform accurate checks and tests. Comply be required to comply with documentation and regulatory procedures and policies. etc. | 4/29/2020 |
| 11426 | Stryker , GA PCBA Manufacturing Engineer, Advanced Operations BS/BA in engineering Exp: 1-2 year(s) |
Be a PCBA Manufacturing Engineer in one of the most exciting and successful areas at Stryker Robotics. Be part of the development and introduction of new products and work extensively with Product Development, Quality and Manufacturing Operations to take a product from design concept through production ramp up. etc. | 4/29/2020 |
| 11427 | Stryker Plainfield, IN Quality Control Technician unspecified Exp: 1-2 year(s) |
Responsibilities: Will perform incoming inspection on components and Electro/mechanical products per company/regulatory specifications. Will work from engineering schematics or blueprints to perform accurate checks and tests. Will be required to comply with documentation and regulatory procedures and policies. Will work across multiple, different IT platforms and Quality Management Systems. etc. | 4/29/2020 |
| 11428 | Stryker , TN PCBA Manufacturing Engineer, Advanced Operations BS/BA in engineering Exp: 1-2 year(s) |
Be a PCBA Manufacturing Engineer in one of the most exciting and successful areas at Stryker Robotics. Be part of the development and introduction of new products and work extensively with Product Development, Quality and Manufacturing Operations to take a product from design concept through production ramp up. Specific responsibilities of the PCBA Manufacturing Engineer include, but are not limited to, the following: Develop processes for the manufacture of PCBAs. etc. | 4/29/2020 |
| 11429 | Stryker , MI Trauma Sales Associate-Detroit BS/BA Exp: 1+ year(s) |
You will get exposure to the proven winning Stryker Trauma culture that delivers Industry leading results in all market segments. You will receive best-in-class formal Trauma training on product portfolio and selling skills which includes on-the-job training in the operating room. You’ll become an expert on surgical procedures by observing well-over 300 cases in your first year. etc. | 4/29/2020 |
| 11430 | Stryker Fort Lauderdale, FL PCBA Manufacturing Engineer, Advanced Operations BS/BA in engineering Exp: 1-2 year(s) |
Be a PCBA Manufacturing Engineer in one of the most exciting and successful areas at Stryker Robotics. Be part of the development and introduction of new products and work extensively with Product Development, Quality and Manufacturing Operations to take a product from design concept through production ramp up. Specific responsibilities of the PCBA Manufacturing Engineer include, but are not limited to, the following: Develop processes for the manufacture of PCBAs. etc. | 4/29/2020 |
| 11431 | Sunrise Pharma Rahway, NJ Regulatory Affairs Associate MS in pharmaceutical manufacturing, regulatory affairs, quality assurance or related Exp: 6 months |
Pharmaceutical Manufacturing seeks a Regulatory Affairs Associate. Resp. include creating & implementing labels for OTC & ANDA submissions, assist in ANDA submissions using eCTD submission software, prepare & maintain annual reports, SOP, deviations & OOS reports, review product complaints & queries & support in developing regulatory strategies & launch OTC products. etc. | 4/29/2020 |
| 11432 | T2Biosystems Lexington, MA Research Associate II MS in microbiology or molecular biology Exp: 1-2 year(s) |
This position will join our growing Microbiology team and will provide aid and expertise in the development of laboratory protocols for the cultivation and characterization of pathogenic organisms. The individual will work with other Microbiology team members to expand on our established protocols and methods to enable the accurate production of test samples for development of novel assays in conjunction with the Assay Development team. This role consists of hands-on execution in the laboratory and data analysis within the Microbiology group and is based in Lexington, MA, reporting directly to the Director of Microbiology, R&D. etc. | 4/29/2020 |
| 11433 | Tandem Diabetes Care Boise, ID Complaint Management Associate BS in biology or chemistry Exp: 1-2 years |
What you’ll be doing: You’ll be working closely with your team to provide a high level of administrative support. This will involve drafting & filing Medical Device Reports to the FDA, maintaining our databases, and supporting departmental audits. The right person for this position will be a quick learner who is detail-oriented. etc. | 4/29/2020 |
| 11434 | TechLab Radford, MA Quality Assurance Officer 1 AS/AA/BS/BA Exp: 0-1 year(s) |
An employee in this position can expect to perform the following duties: Release pre-raw, raw materials and components to departments for use. Create, review, and apply QA Release Labels. Issue and review Master Batch Records (MBRs) in support of Production and BMP schedules. Issue, confirm and approve Expiration Dates of Raw Materials, Components and Finished Products. Review QC results detailed per SOPs, RMSs, and PRSs. Ensure approved documents are issued and controlled. Ensure Controlled Records are controlled and easily retrievable. etc. | 4/29/2020 |
| 11435 | Tecomet Kenosha, WI Maintenance Technician HS diploma or equivalent Exp: 1-2 year(s) |
Essential Duties and Responsibilities: Installs, repairs, overhauls and maintains electronic, electrical, hydraulic, pneumatic, mechanical and/or electro-mechanical machinery and equipment. Observes and tests operation of electronic, electrical, electro-mechanical, hydraulic, pneumatic and/or mechanical devices in order to evaluate and identify operating problems. Fabricates replacement components with direction from section managers/supervisors and/or team leaders in order to affect in-house repairs and/or modify machinery and equipment to improve efficiency. Dismantles equipment and machinery in order to identify, remove, repair and/or replace damaged or deteriorated components, and reassemble equipment. etc. | 4/29/2020 |
| 11436 | Tempus Chicago, IL Clinical Molecular Technologist (Sunday-Wednesday with Shift Diff.) MS in a medical, physical, or biological science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. etc. | 4/29/2020 |
| 11437 | Tempus Chicago, IL Clinical Molecular Technologist MS in a medical, physical, or biological science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. etc. | 4/29/2020 |
| 11438 | Tempus Chicago, IL Molecular Technologist, Infectious Disease BS/MS in a medical, physical, or biological science Exp: 1 year |
What you’ll do: Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. etc. | 4/29/2020 |
| 11439 | Tempus Chicago, IL Laboratory Supervisor, Molecular Infectious Disease BS in a chemical, physical, biological or other laboratory science Exp: 1 year |
What You’ll Do: Provide daily oversight of a cutting-edge molecular workflow to provide high-quality next-generation sequencing data with rapid turnaround times. Monitor laboratory processes to ensure that acceptable levels of analytic performance are maintained, to include review of quality control, instrument and equipment maintenance, and other quality assurance activities. Assure all remedial actions are taken whenever test systems deviate from the laboratory's established performance specifications. etc. | 4/29/2020 |
| 11440 | Tempus Chicago, IL Account Associate BS in biology, other life science, business, or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). Coordinating Medical Affairs report review with physicians after clinical orders. etc. | 4/29/2020 |
| 11441 | Tempus Atlanta, GA Research Laboratory Assistant AS/BS in a biological science Exp: 1 year |
Responsibilities and Duties: A team player helping to construct, implement, and manage multiple tasks. Receives shipments/specimens from couriers, inventories specimens, and documents the receipt of the samples in accordance with laboratory standard operating procedures. Properly identifies specimens that do not follow the proper submission criteria described in the Specimen Processing SOP, and properly documents and reports any issues to team lead, Laboratory Operations and Project Manager for follow up. Ensures the proper handling of specimens in accordance with assigned SOPs including, but not limited to, proper data entry, specimen handling, storage and aliquoting of the specimens. etc. | 4/29/2020 |
| 11442 | Tempus Atlanta, GA Research Associate (AKESOgen) BS in a biological science Exp: 1+ year(s) |
Responsibilities and Duties: A team player helping to construct, implement, and manage multiple experiments. Run automated Nucleic Acid instrumentation, real time PCR, DNA/RNA spectrometer, and genetic scanners. Maintains a clean, safe, and organized lab. Document and maintain records systematically such that they can be easily obtained when needed. Ensure the accuracy of the information before filing. Assist the team leads and scientists in related function. etc. | 4/29/2020 |
| 11443 | Scholar Rock Cambridge, MA Senior Associate Scientist - IHC BS/MS in biology or related Exp: 1-3 year(s) |
Scholar Rock seeks a highly motivated associate with a background in immunohistochemistry to join our research team. The successful candidate will be responsible for supporting and maintaining all aspects of our histopathology workflow, with a strong emphasis on automation. This person will play a key role in our translational science team as they will help establish IHC / IF / ISH assays to characterize drug targets and measure disease endpoints in both patient samples and preclinical models. This position also provides an opportunity to learn new techniques in digital analysis and algorithm development. etc. | 4/29/2020 |
| 11444 | Takeda Cambridge, MA Manufacturing Technician II AS in a life science or engineering Exp: 1 year |
This position reports to Days, 6:00 am – 6:30 pm, 2-2-3, 12.5 hours shift, off every alternate weekend. Due to business need, on select occasions, employees may be required to work overtime. Primary Duties: With general supervision the individual will perform routine and critical manufacturing operations, including but not limited to work functions in Cell Culture, Purification, Solution & Equipment Prep areas. Operates production equipment according to SOPs for the production of clinical and/or commercial products. Responsibilities: This individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Batch Records and Form Preps. etc. | 4/29/2020 |
| 11445 | Boston Scientific Minnetonka, MN Quality Engineer I Job BS/BA in engineering or related Exp: 0-2 years in related |
This role will assist in developing and refining failure analysis methodologies as a means of advancing comprehensive understanding of product performance to improve patient outcomes. This position will identify, analyze, investigate, monitor and document patterns and trends in complaint data. Communicate and educate management, R&D, Design Assurance, Ops Quality, Marketing, Sales and other departments about product performance and escalations. Ensure that information and insights gained from product investigations and corrective actions is fed back to the R&D, Design Assurance and Marketing organizations as part of the risk management and design input process. | 4/25/2020 |
| 11446 | Boston Scientific Minnetonka, MN Product Analyst I Job BS/BA or MS Exp: BS: 0-2 years, MS: 0 years |
Investigates and resolves product complaints of all products. Maintains complaint databases and complaint files, runs trend reports. Facilitates product complaint investigations. Confirms complaint, follows up to get additional information when needed. Makes initial MDR decision, under supervision. Reviews file for completeness, closes and files the complaint folder. Interfaces with various internal and external entities such as Manufacturing and R&D to assist with obtaining complete information or product complaint analysis. | 4/25/2020 |
| 11447 | AvantGen San Diego, CA Laboratory Assistant HS Diploma/GED Exp: 0 years, college coursework |
The scope of work for this position includes general lab support operations, such as stocking lab supplies, cleaning and autoclaving glassware, prepararation of media and buffers, and perform basic molecular biology experiments, such as PCR, cloning, and plasmid preps. | 4/25/2020 |
| 11448 | Avantor Chandler, AZ JIT Technician HS Diploma/GED Exp: 1-2 years in customer facing environment |
The Technician is responsible for providing a high level of accuracy, and contributing to a culture of safe work and superior customer service. Accurately records and communicates information to internal and external teams. Shares with team any changes in demand to maintain appropriate service levels. Builds positive relationships with both internal and external customers | 4/25/2020 |
| 11449 | Avantor Fort Worth, TX Lab Support Technician HS Diploma/GED Exp: 1-2 years in lab setting |
The laboratory technician prepares and weighs samples for testing and analysis. May setup and conduct tests, assays, and other protocols under the direction of a laboratory services manager, researcher, or scientist. Follow Standard Operating Procedures (SOPs) and Good Laboratory Practices (GLPs). Ensure all laboratory equipment and work areas are clean, sterile, and in proper working order. May be responsible for calibration of instruments and also involved in media prep. | 4/25/2020 |
| 11450 | Avantor Rensselaer, NY Inventory Technician HS Diploma/GED Exp: 1-2 years in customer facing environment |
The Technician is responsible for providing a high level of accuracy, and contributing to a culture of safe work and superior customer service. Accurately records and communicates information to internal and external teams. Shares with team any changes in demand to maintain appropriate service levels. Builds positive relationships with both internal and external customers | 4/25/2020 |
| 11451 | Avantor Rensselaer, NY Inventory Technician HS Diploma/GED Exp: 1-2 years in customer facing environment |
The Technician is responsible for providing a high level of accuracy, and contributing to a culture of safe work and superior customer service. Accurately records and communicates information to internal and external teams. Shares with team any changes in demand to maintain appropriate service levels. Builds positive relationships with both internal and external customers | 4/25/2020 |
| 11452 | Avantor Devens, MA Cleanroom Assembly Technician, 1st shift HS Diploma/GED Exp: 0-2 years in cleanroom |
Under direction of the cleanroom lead and the area supervisor, the Cleanroom Assembly Technician will build a wide-range of Single-Use assemblies that meet or exceed customer requirements. Uses a variety of manufacturing and measuring equipment such as tube cutters, rulers, oetiker tools, and heat sealers. Follows engineering drawings, products work instructions, standard operating processes to accurately and efficiently build product and maintain associated data throughout the process. | 4/25/2020 |
| 11453 | Avantor Radnor, PA B2B Assoc Tech Proj Mgr, eBusiness (US) College degree in related Exp: 1-3 years app. Experience |
The Associate Technical Project Manager will be responsible for managing small to medium internal customer eProcurement integration projects. This role will also assist in developing standards and documentation for external integrations to VWR systems, analyzing current business processes and technologies, and driving improvements within the customer Procure to Pay life cycle. | 4/25/2020 |
| 11454 | Avantor Rensselaer, NY Inventory Technician HS Diploma/GED Exp: 1-2 years in customer facing environment |
The Technician is responsible for providing a high level of accuracy, and contributing to a culture of safe work and superior customer service. Accurately records and communicates information to internal and external teams. Shares with team any changes in demand to maintain appropriate service levels. Builds positive relationships with both internal and external customers | 4/25/2020 |
| 11455 | Arrowhead Pharma Madison, WI Associate Scientist, Discovery Analytical Chemistry BS/BA in chemistry or biology Exp: 1 year in preping biological samples |
Arrowhead is seeking a highly motivated associate analytical chemist to join our growing Discovery Chemistry team. The successful candidate will be tasked with biological sample preparation and running HPLC to support ongoing discovery activities. S/He will be expected to: Follow the instructions to prepare samples from various biological matrix such as plasma, urine, tissues etc. Perform sample analysis using HPLC | 4/24/2020 |
| 11456 | Arrowhead Pharma Madison, WI Associate Chemist, CMC MS in chemistry/biochemistry Exp: 0-3 years |
We have an immediate opening for an Associate Scientist to work as a Chemist in the Chemistry, Manufacturing, and Controls Group focusing on oligonucleotide synthesis development. This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates. | 4/24/2020 |
| 11457 | Arrowhead Pharma Madison, WI Associate Production Chemist HS Diploma/GED Exp: 0-5 years in similar position |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. The successful candidate will be expected to: Follow batch records, SOPs, and work instructions to detail. Document all operations in batch records and notebooks. Comply with GMP protocols | 4/24/2020 |
| 11458 | Arthrex Cleveland, OH Vet Sales Associate BS/BA Exp: 1 year in outside sales |
The Arthrex Veterinary Sales Associate is responsible for generating sales of products and equipment to both existing veterinarians and new customers within an assigned sales territory. The Arthrex Veterinary Sales Associate plans and makes sales calls, and selects products and programs that motivate customers to buy products. | 4/24/2020 |
| 11459 | Arthrex Ave Maria, FL Labeling Systems Technician - Ave Maria Associates Degree preferred Exp: 0-2 years in industry |
Troubleshoots hardware and software problems related to labeling operations, including, but not limited to, barcode scanners, labeling systems, labels, and printers. Performs equipment calibration, maintenance, and qualification activities. Participates in the execution of Arthrex validation protocols related to labeling operations, including, but not limited to, label printing, barcode scanning, and barcode inspection. Helps determine process capability of new equipment through execution of approved protocols and assures defined parameters are incorporated into respective operating procedures. | 4/24/2020 |
| 11460 | Arthrex Sandy Springs, SC Clean Room Assembler HS Diploma/GED Exp: 0-2 years in manufacturing/packaging |
Performs manual and fixture assisted device assembly and packaging on medical device components, kits, convenience packs and / or any clean room specific device assembly as assigned. Performs placement of components onto the blister trays and die cut restraints. Performs label application onto packaging constructs. Performs supplemental label application, blister loading, pouch and blister sealing and visual seal inspection | 4/24/2020 |
| 11461 | Arthrex Sandy Springs, SC Engineer - Packaging BS/BA in engineering (packaging, industrial, etc.) Exp: 1-3 years in process/packaging engineering preferred |
Responsible for supporting Packaging Operations and Packaging and Manufacturing Process Engineers on the development and execution of sterile packaging processes including material, design, and equipment validations. Assist in the selection, installation, and validation of medical device packaging equipment. Write and execute engineering studies/DOEs, validation IOQ/PQ protocols, gage R&Rs for packaging equipment processes, tools/fixtures, and inspection apparatus including: pouch sealing, blister tray sealing, burst testing, pull testing, dye penetration testing, print & apply, etc. | 4/24/2020 |
| 11462 | ArunaBio Athens, GA Biomanufacturing Associate BS/BA in biological sciences or engineering Exp: 0-2 years in industry |
The Biomanufacturing Associate supports the the manufacturing efforts of ArunA Bio, and must work collegially and collaboratively as part of a larger team. The position requires the individual to carry out complex stem cell manufacturing with an advanced degree of detail, and in accordance with established SOPs, cGMPs, and safety regulations. The individual will work as a member of a team responsible for performing all bioprocessing workflows. | 4/24/2020 |
| 11463 | ArunaBio Athens, GA Research Associate I – Preclinical R&D Team BS/BA in biological sciences Exp: 1-2 years in lab |
The successful candidate would participate in a wide variety of research activities including animal care, animal technical procedures, animal health evaluations, and research data collection.Perform routine, pre-operative, and post-operative care of research animals. Assist during and/or perform surgical and other technical procedures with rodents | 4/24/2020 |
| 11464 | ArunaBio Athens, GA Research Associate I – CNS Targeting and Drug Delivery BS/BA in biological sciences or engineering Exp: 1-2 years in lab |
The Research Associate I will perform cell culture, execute analytical and functional assays to characterize exosome modifications and assist with in vivo procedures. Perform mammalian cell culture using sterile technique. Use a variety of equipment such as pipettors, balances, ultracentrifuges, laminar flow hoods, incubators, microscopes, centrifuges, plate readers, and nanoparticle tracking analysis equipment such as NanoSight | 4/24/2020 |
| 11465 | Arvinas New Haven, CT Laboratory Assistant, Formulation R&D BS in sciences Exp: 1-3 years in pharma R&D |
In the role as a laboratory assistant, you will prepare pharmaceutical formulations used in animal pharmacology and pharmacokinetic studies, and will work closely with compound management and in-life colleagues to make sure that dosing materials are available as needed. When issues related to formulation arise, you will serve as a primary problem-solving Formulation R&D contact for those in other disciplines. | 4/24/2020 |
| 11466 | AskGene Pharma Camarillo, CA Associate Scientist / Scientist – Cell Line Development MS in biological/chemical science or engineering Exp: 1-3 years |
In this role you will primarily be responsible for CHO cell line generation and process development. Plasmid DNA preparation. CHO cell line development for expression of monoclonal antibodies, bispecific antibodies, Fc-fusions and other therapeutic proteins. CHO cell culture process development | 4/24/2020 |
| 11467 | AskGene Pharma Camarillo, CA Associate Scientist – Upstream Process Development MS in biological/chemical science or engineering Exp: 1-3 years |
Reporting to the director of the upstream process Development team, you will be responsible for the cell line/upstream process development to support process development and manufacturing activities (e.g. stable cell line generation and characterization and various bioreactors operation). You will also involve in tech transfer, process scale up and CMO management. This is an entry level hands-on scientist position. You will design and carry out experiments, perform general laboratory activities that include the routine maintenance of equipment and will keep an accurate laboratory record (lab notebook) of all experiments. You will also write technical reports when needed. | 4/24/2020 |
| 11468 | Associates of Cape Cod East Falmouth, MA Technical Services BET Specialist (2 openings) BS/BA in chemistry/biology Exp: 0-2 years in related |
Provide technical support for endotoxin and glucan detection products. This includes answering questions, troubleshooting for current ACC customers. Troubleshoot/triage issues, problems and complaints in a timely manner, documenting them in CRM and providing trending to manager. Frequent follow up on all issues ensuring timely resolution of the customer’s issue. Knowledge of relevant instrumentation and softwares used for endotoxin and glucan detection by the end users | 4/24/2020 |
| 11469 | Associates of Cape Cod East Falmouth, MA Qjuality Control Analyst I BS in sciencecs Exp: 0-2 years lab experience |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results | 4/24/2020 |
| 11470 | Associates of Cape Cod East Falmouth, MA Production Technician I (Saturday - Wednesday) HS Diploma/GED Exp: 0-2 years in related |
In this position you will perform routine manufacturing operations for the manufacture of ACC and SKK commercial products. You will carry out cGMP manufacturing operations based on Standard Operating Procedures. You would need to come onboard initially Monday thru Friday for a few months to train in gowning, filling, crimping, lyo, oven operation, and autoclave operation | 4/24/2020 |
| 11471 | Astrazeneca Gaithersburg, MD R&D Associate II/Associate Scientist I - Formulations - BPD MS in chemistry/biological science or engineering Exp: 0 years |
Laboratory activities include buffer and protein solution preparation, pipetting and aseptic operations in a biosafety cabinet. Analytical methods that are used routinely include HPLC (reversed-phase, size-exclusion, and ion-exchange chromatography), UV-visible spectroscopy, HIAC and MicroFlow Imaging for sub-visible particle counting.The candidate will work under general supervision and his/her work will be reviewed for accuracy and soundness of technical approach. The candidate will make detailed observations, summarize results in tables and figures, document data into lab notebooks, and analyze data and interpret results. | 4/24/2020 |
| 11472 | Astrazeneca Gaithersburg, MD Associate Scientist I/II MS in mechanical/biomedical/chemical engineering, or pharma sciences Exp: 0-2 years |
The candidate will be a part of Dosage Form Design and Development group working on combination device characterization and functionality, development of novel technologies, and transforming scientific knowledge / analysis into practical implementations. Innovate, develop and evaluate device characterization techniques and technologies as they relate to device development requirements. Perform test method qualification and method transfer to GMP testing group in support of device verification & validation testing. | 4/24/2020 |
| 11473 | Astrazeneca Gaithersburg, MD Pilot Production Technician I/II - BPD Associates or Bachelors Exp: BS: 0 years, AS: 1-2 years |
As a pilot production associate in the Clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities. | 4/24/2020 |
| 11474 | Astrazeneca Gaithersburg, MD Associate Scientist I, Purification Process Sciences MS in related Exp: 1 year in protein/viral vector purification |
Develop and characterize purification processes for the manufacture of biopharmaceuticals (viral vectors, antibodies and other proteins) in early stage clinical development. Be responsible for a portion of a purification process development project. Make observations, analyze data and interpret results. Maintain accurate records of experimental results, review, analyze, and interpret experimental data. | 4/24/2020 |
| 11475 | Astrazeneca Frederick, MD Production Technician I - Night Shift - Operations BS/BA Exp: 0-1 yearas |
Operation of upstream / downstream / central services processing equipment according to established SOPs. This equipment includes but is not limited to bioreactors, TFF skids, biological safety cabinets, incubators, chromatography skids, UFDF skids, autoclaves, washers, and product hold tanks. Upstream / downstream / central services processing according to established manufacturing production records (MPRs & SPRs) in accordance with cGMPs. | 4/24/2020 |
| 11476 | Astrazeneca Frederick, MD Production Technician II - Day Shift - Operations BS/BA Exp: 1-3 years |
Proven ability to perform all process steps of upstream / downstream / central services production operations and act as the primary trainer of those with less experience (and may act as interim Lead as required). Ability to generate SOPs, MPRs, and SPRs for equipment and procedures used in the manufacture of biological based products. Execution of validation protocols as required as well as the ability to execute projects with minimal instruction and strategic direction. | 4/24/2020 |
| 11477 | Astrazeneca Frederick, MD Production Technician I - Day Shift - Operations BS/BA Exp: 0-1 years |
Operation of upstream / downstream / central services processing equipment according to established SOPs. This equipment includes but is not limited to bioreactors, TFF skids, biological safety cabinets, incubators, chromatography skids, UFDF skids, autoclaves, washers, and product hold tanks. Upstream / downstream / central services processing according to established manufacturing production records (MPRs & SPRs) in accordance with cGMPs. | 4/24/2020 |
| 11478 | Astro Pak Downey, CA Associate Technician - Ontario 1 year technical training/certification course Exp: 1 year in related |
The Associate Technician performs entry-level Field Services duties to gain knowledge and understanding of cleaning and passivation of vessels and piping. Under supervision, Associate Technicians work together to complete the process in a safe and expedient manner to prevent unnecessary down time of the customer equipment. Proper calculations and installation of Astro Pak equipment plus vigilant operation of said equipment is necessary. | 4/24/2020 |
| 11479 | Astro Pak Raleigh, NC Associate Technician - North Carolina 1 year technical training/certification course Exp: 1 year in related |
The Associate Technician performs entry-level Field Services duties to gain knowledge and understanding of cleaning and passivation of vessels and piping. Under supervision, Associate Technicians work together to complete the process in a safe and expedient manner to prevent unnecessary down time of the customer equipment. Proper calculations and installation of Astro Pak equipment plus vigilant operation of said equipment is necessary. | 4/24/2020 |
| 11480 | ATEC Spine Carlsbad, CA Material Handler HS Diploma/GED Exp: 1-3 years in inventory Control |
This position is responsible for creating purchase orders and shipping inventory for outside processing. Counts and verify parts for outside processing. Packages parts safely for shipping. Creates purchase order for outside processing. Files all work and purchase orders. Delivers products to vendors when needed. | 4/24/2020 |
| 11481 | Athenex Clarence, NY Warehouse Associate HS Diploma/GED Exp: 1-3 years in warehouse environment |
The Warehouse Associate is responsible for the physical process of goods pertaining to the receipt, storage and shipment in and out of the warehouse. This includes site inventory of raw materials, work-in-process and finished goods as well as the maintenance, repair and operating supplies. Inventory must be current and accurate in status, warehouse, quantity, lot ID and warehouse location. | 4/24/2020 |
| 11482 | Atomwise San Francisco, CA Research Associate in Biochemistry MS in biological/chemical science or engineering Exp: 1-3 years |
Atomwise is looking for a Research Associate to support our scientific and business development teams by performing literature and database analyses and providing insightful reports and research plans. Search scientific literature, databases and biochemical structural data. Prepare scientific research plans. Understand the experimental design and methodologies in life science publications | 4/24/2020 |
| 11483 | Atreca South San Francisco, CA Research Associate I/II, Target ID (Temporary) BS in biology Exp: 1-2 years in lab |
In this position, the successful candidate will apply her/his skills and expertise to support Atreca’s oncology team in discovering the unique targets of patient-derived antibodies. In particular, the successful candidate contributes by maintaining in-vitro cell cultures and operating robotics for high throughput target-ID assays. | 4/24/2020 |
| 11484 | Quotient Sciences Garnet Valley, PA Project Coordinator BS/BA Exp: 1-2 year(s) |
Due to growth and expansion, we have an exciting opportunity for a Project Coordinator to join the Project Management Department. As the Project Coordinator, you will work on multiple projects with Project Managers and be responsible for coordinating project activities internally and externally with customers and vendors. Tasks and responsibilities will include: Assist with the development and maintenance of project plans. Assist with the organization of meetings, development of meeting agendas, minutes and action items. etc. | 4/22/2020 |
| 11485 | Quotient Sciences Boothwyn, PA Analytical Scientist II MS in chemistry Exp: 0-2 years |
The position may reside in any one of the functional areas and carry out the responsibility under some supervision: Operate and troubleshoot the following instruments/equipment to test pharmaceutical samples: HPLC/UPLC. Dissolution apparatus. Karl-Fisher water content titrator. GC. FTIR. UV. Other analytical instruments as directed. Follow analytical test methods, compendial methods, experimental procedures and SOP’s. etc. | 4/22/2020 |
| 11486 | Quotient Sciences Boothwyn, PA Analytical Scientist I BS in chemistry Exp: 0-3 years |
The position may reside in any one of the functional areas and carry out the responsibility under some supervision: Analytical method development, validation, and transfer activities. Formulation development work including Material characterization and physical testing. API/raw material sampling and testing, In-process and finished product testing, cleaning verification swabbing and testing. etc. | 4/22/2020 |
| 11487 | Quotient Sciences Garnet Valley, PA Recruitment Coordinator unspecified Exp: 1+ year(s) |
The Recruitment Coordinator position is a critical addition to the US recruitment function and the Human Resources team. The successful candidate will engage in scheduling, planning and executing recruitment activities throughout 3 US based sites located in the greater Philadelphia, Pennsylvania region and Miami, Florida. This highly visible position allows for both local and global visibility and will assist in shaping the future initiatives within the talent acquisition function. etc. | 4/22/2020 |
| 11488 | Regeneron Tarrytown, NY R&D Associate-VI Next - Oligonucleotides MS/MA Exp: 1-2 year(s) |
We are seeking a highly skilled and motivated associate to join our new group devoted to the drug discovery and technology development specifically in the area of oligonucleotide therapeutics such as antisense oligonucleotides and siRNAs. The responsibilities of this position include designing and screening of oligonucleotide candidates as well as carry out research on technology development to improve chemistry and delivery of nucleic acid therapeutics (siRNA/ASO). Candidates are expected to work independently in a creative, collaborative, and dynamic team environment, with strong support for skill and career development. etc. | 4/22/2020 |
| 11489 | Rejuvenate Bio San Diego, CA Research Assistant BS/BA in biology, biochemistry, biomedical engineering or related Exp: 1+ year(s) |
Rejuvenate Bio is looking for a highly-motivated individual to join our energetic team and accelerate the development of our therapies. There search assistant position will directly support efforts to drive forward our future commercial offerings working with other RA's and scientists. The applicant will be performing standard molecular biology procedures as well as more advanced cell culture and virus creation. The role reports to senior or principal scientists at Rejuvenate Bio. | 4/22/2020 |
| 11490 | Renaissance Lakewood, NJ Compounder, 2nd shift HS diploma or equivalent Exp: 1-3 year(s) |
Entry level position to Compounding Department with emphasis on ensuring that equipment used to process aseptic and non-aseptic products has been cleaned, sanitized or sterilized, as required by specific documentation or procedures. This entails performing automated and manual equipment cleaning prior to sterilization, placing cleaned equipment into autoclaves, starting and monitoring autoclaves, unloading equipment from autoclaves, and delivering equipment to areas of use. etc. | 4/22/2020 |
| 11491 | Renaissance Lakewood, NJ Compounder, 3rd shift HS diploma or equivalent Exp: 1-3 year(s) |
The Compounder's primary responsibility is for the execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. Hours are 11:00 pm - 7:30 am. Responsibilities: Follow manufacturing procedures to process bulk product. Batches to be made right the first time. Follow manufacturing procedures specific to the task being performed. etc. | 4/22/2020 |
| 11492 | Rheos Medicines Cambridge, MA Research Associate BS in cellular or molecular , immunology, or related Exp: 0-5 years |
The Research Associate is responsible for initiating, designing and executing experiments that support scientific projects relevant to different immune related diseases. Ability to perform a variety of immune cell based in vitro assays utilizing both cellular and molecular biology techniques. Effectively communicate results and conclusions to cross-functional project teams. etc. | 4/22/2020 |
| 11493 | Ribon Therapeutics Cambridge, MA Research Associate/Senior Research Associate – Biological Sciences MS in biology, biochemistry or related Exp: 1-3 year(s) |
The successful candidate will serve as an integral member of a multidisciplinary drug discovery project team developing novel small molecule inhibitors for monoPARPs and NADome targets. This position by will be reporting to a scientist in the Biological Sciences group to support target validation. He or she will employ a variety of molecular and cell biology techniques to understand target biology and develop cell-based assays for small molecule inhibitors. etc. | 4/22/2020 |
| 11494 | Roche Mansfield, OH Field Engineering Specialist - Molecular Diagnostics BS in chemistry or biomedical, mechanical or electrical engineering Exp: 1-2 year(s) |
The Roche Support Network group is committed to providing industry-defining support to its customers. As a Field Engineering Specialist, you will have the opportunity to travel and demonstrate your expertise as a technical repair and/or installation specialist for Roche assigned product lines, and provide valued service to your laboratory customers in an assigned territory. The Field Engineering Specialist, Clinical Chemistry in the Roche Support Network, position serves as a technical repair or installation specialist for Roche products for assigned product lines and geographies. etc. | 4/22/2020 |
| 11495 | Roche Tuscon, AZ Technician Instruments AS/AA in electronics, electrical engineering, or related Exp: 1-3 year(s) |
A Technicians responsibilities include testing of Company products following documented procedures to assure conformance to specifications and standards, completing written records of work done, and identifying and documenting non-conformances in piece parts, assemblies and test results. In addition, an Associate Technician must be able to effectively troubleshoot routine test failures to the subassembly level, consulting with more experienced technicians as needed. Responsibilities may also include assembly of Company products. etc. | 4/22/2020 |
| 11496 | Roche Branchburg, NJ Scientist BS in the life sciences, engineering, or related Exp: 0-1 year(s) |
The ‘Case Investigation and Resolution’ department is the Center of Excellence for the resolution of global product complaints. The Scientist (CIR) is responsible for effective and timely resolution of global cases, including complaint investigations, risk assessments, case documentation, trending analysis and preparing reports, ensuring regulatory compliance and optimal levels of customer satisfaction. Also participates in the On-Boarding of new employees by providing product and process training and support. The ideal candidate has strong technical knowledge, expertise of assay workflow and system functionality, enjoys troubleshooting, and has a problem solving mindset. etc. | 4/22/2020 |
| 11497 | Roche Tuscon, AZ Instrument Assembler HS diploma or equivalent Exp: 0-1 year(s) |
Responsibilities: Ensure accurate assembly of components and subassemblies per production drawings and documents while maintaining accurate manual and electronic records. Adhere to manufacturing schedule in order to meet deadlines while sustaining quality, cost, delivery, and safety metrics. Control accurate inventory on assembly line. Adhere to company policies in order to ensure successful manufacturing goals. etc. | 4/22/2020 |
| 11498 | Roche Branchburg, NJ Diagnostic Tech Associate (2nd shift) HS diploma or equivalent Exp: 0-2 years |
Job requirements will include ability to perform in the aseptic environment. Wear personal protective equipment, such as eye, foot, lab coat, mask, gowning coveralls. DIAG TECH ASSOCIATE- 2nd shift: For our Second Shift we are looking for someone who is willing to work Monday to Friday with normal hours from 3:00PM until 11:30PM. etc. | 4/22/2020 |
| 11499 | Roche Indianapolis, IN Maintenance Technician (2nd Shift) HS diploma or equivalent Exp: 1 year |
As a Maintenance Technician, you will dismantle, adjust, repair and assemble equipment according to drawings, operation and maintenance manuals, or sketches. You will assist in the determination of the root causes of failures and provide input on preventive/predictive options to eliminate/limit like failures. You will work under the guidance of your supervisor or experienced team members, perform simple electrical and mechanical troubleshooting to determine problems with equipment used in the manufacturing process. etc. | 4/22/2020 |
| 11500 | Roche Branchburg, NJ Diagnostic Technician Associate 1st Shift Final Packaging HS diploma or equivalent Exp: 0-2 years |
Responsibilities: Assembles totes, cartons, platforms, and associated packaging and filling components. Under direction of area supervision, assist in setting up Packaging/Filling lines, and staging for production activities. Perform visual inspection for visible defects of components produced in the Filling Area and components being placed into kits in the Packaging Area. Place components (filled vials, inserts, barcode clips ect.) into totes and or kits per instructions in applicable SOPs and Production Records. etc. | 4/22/2020 |
| 11501 | Rocket Pharma Cranbury Township, NJ Manufacturing Associate 1 BA/BS in biotechnology, chemical engineering, or a life science Exp: 0-2 years |
This technical position is a key role in manufacturing operations. The ideal candidate will have less than 2 years of experience performing large scale cGMP clinical or commercial manufacturing of viral vectors, biologics or monoclonal antibodies at a leading pharma or biotech organization. Candidates with no previous experience who meet the educational requirements are encouraged to apply. As a Manufacturing Associate, you will be responsible for large scale manufacture of viral vector therapies. Additional responsibilities include set-up, operation and cleaning of equipment, equipment and process monitoring, upkeep of cGMP equipment and manufacturing area, completing cGMP batch documentation, and receiving cGMP materials from the warehouse. etc. | 4/22/2020 |
| 11502 | Sangama Therapeutics Brisbane, CA Development Associate II BS in pharmaceuticals, biology, or related Exp: 1-2 year(s) |
We are seeking a motivated and hard-working Research Associate I/II for our Technical Operations Analytical Development Group. In this role, you will perform key gene- and cell-based potency and strength assays to support AAV gene therapy; troubleshoot and optimize particular assays as needed; assist in the development of new analytical methods to determine the strength, purity and/or potency of viral vector preparations; and perform other tasks such as biolab equipment maintenance and minimal supply ordering. This position requires experience in good laboratory and documentation practice. etc. | 4/22/2020 |
| 11503 | Renaissance Lakewood, NJ Materials Coordinator I, Temporary HS diploma or equivalent Exp: 0-2 years |
The Materials Coordinator will assist in the efficient receipt, storage, movement and inventory of items throughout the Warehouse. This is a temporary position. Responsibilities: Perform several tasks simultaneously. Must be able to organize and prioritize work in order to accomplish tasks assigned. Picks and stages raw materials/ components as required to support work orders on the production schedule. Complete material returns and issue materials to orders in ERP system. Assist with receiving of materials. etc. | 4/22/2020 |
| 11504 | Repligen Waltham, MA Manufacturing Associate II- Biomanufacturing 2nd Shift BS in a biological science Exp: Not necessary for BS candidates |
The successful candidate will play a key role in ensuring that the department’s production and quality goals are met. Applicants must have strong technical knowledge and problem-solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. Experience working in a GMP/document-controlled environment would be beneficial. Attention to detail, and the ability to work in a team environment are essential. Candidates must be willing and able to learn new manufacturing processes as the company grows and also to work overtime. etc. | 4/22/2020 |
| 11505 | Repligen Rancho Dominguez, CA Assembler-I HS diploma or equivalent Exp: 0-1 year(s) |
This assembly position performs a wide variety of fiber assembly, filtration product assembly or sub-assemblies. Determines and/or follows methods and sequence of operations in performing fiber bundling, filter potting, filter welding, fitting on assembly units and packaging. The employee also works as a team member in whatever capacity and job function is required to deliver a quality product to our customer in a timely fashion. Perform manual assembly of complex fiber, membrane, and polycarbonate components. Follow detailed manufacturing and assembly procedures. etc. | 4/22/2020 |
| 11506 | Repligen Waltham, MA ELISA Manufacturing Associate Level 2 AS/BS Exp: 1-2+ year(s) |
This position is in Repligen’s ELISA group. The successful candidate will be responsible for the manufacture of ELISA kits and its components as well as in-process testing. The individual must be able to follow oral and written instructions accurately and complete tasks in a timely manner. Experience working in a GMP/ISO/document-controlled environment would be beneficial. Attention to detail and the ability to work in a team environment are essential. Candidates must be willing and able to learn new manufacturing processes as the company grows. Responsibilities: Plate coating, conjugate production, buffer preparation and kit assembly. Dispensing, capping, labeling and packaging of reagents. etc. | 4/22/2020 |
| 11507 | Repligen Waltham, MA Manufacturing Associate I - OPUS 2nd shift unspecified Exp: 1-3 year(s) |
This position will function in Repligen's OPUS Column Packing groups. Cross training into other departments may be required based on the changing needs of the department. The successful candidate will play a key role in ensuring that the department's production and quality goals are met. Applicants must have strong technical knowledge and problem solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. etc. | 4/22/2020 |
| 11508 | Regeneron Tarrytown, NY R&D Associate - VI Next MS in immunology, molecular biology, biochemistry or related Exp: 0-2+ years |
We are seeking a R&D associate with a strong foundation in immunology to join our VI Next group. The candidate must have experience with animal handling, injections and tissue harvesting. Experience designing flow cytometry panels and FACS analysis software is strongly preferred. This position will involve work on multiple projects simiulataneously, so excellent record-keeping and time management are very important. etc. | 4/22/2020 |
| 11509 | Regeneron Tarrytown, NY Process Development Associate II - Cell Culture Data Analytics BS/BA in chemical engineering or computer science or engineer Exp: 0-5 years |
The Cell Culture Development group of the Process Development organization is actively searching for a motivated person with a record of accomplishment and/or a strong interest in analyzing bioprocessing data. This position presents the opportunity for statistical and data science innovation to enhance the efforts of a dynamic and data driven group. Starting level would be determined by background experience. etc. | 4/22/2020 |
| 11510 | Regeneron Tarrytown, NY R&D Associate - Protein Biochemistry BS/MS in biochemistry, biophysics, chemical engineering. Or related Exp: 0-2+ years |
We are seeking an R&D Associate with demonstrated experience using different biophysical and biochemical methods to quantify the physicochemical properties of proteins. The qualified candidate will be responsible for providing in-depth characterization of therapeutic proteins to support research, developability assessments, and early development programs through IND. The candidate is expected to participate in method development and technology innovation efforts aimed to enhance our understanding of biotherapeutic proteins and specifically address both upstream research and late-stage program needs. etc. | 4/22/2020 |
| 11511 | Quotient Sciences Garnet Valley, PA Recruiter BS/BA Exp: 1+ year(s) |
Reporting into the Senior Manager, Talent Acquisition, this Recruiter will be a key figure in the US expansion of our rapidly growing team. This individual will have the opportunity to support a broad number of professional functions across 3 sites in Pennsylvania and Florida. Main tasks and responsibilities: Assists the Senior Manager, Talent Acquisition in delivering recruitment strategy through Full-Life cycle recruitment of candidates by partnering with hiring managers and other appropriate managers when a vacancy arises. Supports the generation and maintenance of internal and external job postings; determines effective advertising mediums; places appropriate advertisements. etc. | 4/22/2020 |
| 11512 | Santa Cruz Biotechnology Dallas, TX Customer Service Representative AA/BA/BS in biology or business administration Exp: Entry level |
SCBT has an immediate opening for an entry level Customer Service Representatives at its Dallas, TX Headquarters campus. This position performs telephone customer support, order processing, and data entry functions. The current shift available for this position is the early afternoon to early evenings shift, Monday through Friday. This is a full time position with career advancement opportunities within the company. Santa Cruz Biotechnology, Inc (SCBT) is a world leader in the development of products for the biomedical research market. For the past twenty-five years, SCBT has focused on the development of research antibodies, biochemicals, labware and it has more recently expanded into animal health care products. etc. | 4/22/2020 |
| 11513 | Santa Cruz Biotechnology Dallas, TX Technical Sales Representative BS in biology, chemistry, or related Exp: 1-2 year(s) |
A Technical Sales Representative is responsible for inside sales activities with customers via phone, email and live chat. The ideal candidate will actively make outgoing calls to speak to customers and build relationships with the goal of increasing sales. This is a full time position. Training on our extensive product line and related protocols is provided. etc. | 4/22/2020 |
| 11514 | Santa Cruz Biotechnology Paso Robles, CA Animal Health Marketing and Sales Representative BS/MS in animal science or related Exp: Entry level |
SCAH/SCBT has an immediate opening for an entry level Animal Health Sales Representative at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. Some intermittent weekend work is required. Required Skills: Ability to work independently to achieve sales growth for the Santa Cruz Animal Health product line in the U.S. Ability to professionally receive inbound customer calls regarding orders and technical questions. Capacity to identify and source new products to broaden our product line. etc. | 4/22/2020 |
| 11515 | Pyramid Laboratories Costa Mesa, CA Manufacturing Technician No degree required Exp: 1+ year(s) |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. PRINCIPAL DUTIES: Familiar with related GMP procedures and requirements, as directly related to the position. Ensure that appropriate procedures and processes are utilized without unauthorized modifications. etc. | 4/21/2020 |
| 11516 | Quidel San Diego, CA Process Analyst I BA/BS in chemistry, biology, or related Exp: 0-2 years |
Under general supervision, the Process Analyst I is responsible for analyzing device and subassembly testing data and ensuring continuity of data entry. The position is responsible for developing methods/reports to analyze data to predict product quality and summarize product performance periodically. The position is also responsible for assisting in product quality improvements, supporting resolution of field-reported performance issues, transferring and validation of new products, and implementation of product improvements which increase quality, lower cost, and increase manufacturing capacity. etc. | 4/21/2020 |
| 11517 | Quidel San Diego, CA Production Chemist (Particle Chemistry) MA/MS Exp: Not necessary for MS/MA candidates |
Quidel is searching for a Production Chemist to work in our Particle Chemistry Lab in the Mira Mesa area of San Diego. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. ESSENTIAL FUNCTIONS: Purification sof various antbodies via different liquid chromatography procesuders. Conjugation of antibodies. etc. | 4/21/2020 |
| 11518 | Quidel San Diego, CA Quality Assurance Specialist BS/BA in science Exp: 1-3 year(s) |
Under the supervision of the Supervisor/Manager, the scope of this position is responsible for carrying out the daily operations of the Batch Record Department as defined by the Quidel Quality Management System and within defined company policies, procedures and regulatory requirements. ESSENTIAL FUNCTIONS: Responsible for managing throughput of all QA reviewed Device History Records, and others as assigned. Responsible for reporting of monthly trending metrics, and developing weekly priorities. Work with groups within the organization to get corrections and clarifications to Device History Records. etc. | 4/21/2020 |
| 11519 | Quanterix Billerica, MA Research Associate - Accelerator BS in chemistry, biochemistry, or life science Exp: 1-3 year(s) |
To continue our solid growth, we are seeking a talented and highly motivated Research Associate to join our growing organization. This position will be part of our Accelerator Laboratory Services team. In this role, you will be developing, optimizing and troubleshooting new biomarker assays for Quanterix's proprietary Simoa technology. Key Responsibilities: Apply your laboratory skills and experience to generate high quality data in support of a diversity of projects, which will include both immunoassay development and validation as well as testing and analysis of clinical samples using commercial kits. etc. | 4/21/2020 |
| 11520 | Quanterix Billerica, MA Manufacturing Associate BS in chemistry, biology, or related Exp: 1+ year(s) |
To continue our solid growth, we are seeking a talented and highly motivated Manufacturing Associate to join our growing organization. This role spans a broad range of activities within the manufacturing operations team at Quanterix. In the role, process responsibilities range from complex protein conjugations to diluent formulation and filling and kitting activities to support a diverse assay menu. Key Responsibilities: Responsible for meeting manufacturing schedule requirements within a fast-paced manufacturing operation with primary activities being: bottle/vial filling, buffer diluent formulation and protein conjugation. etc. | 4/21/2020 |
| 11521 | Quanterix Billerica, MA Quality Control Analyst I BS in chemistry, biochemistry, or biology Exp: 1+ year(s) |
To continue our rapid growth, we are seeking a talented and highly motivated Quality Control (QC) Analyst to join our growing organization. This position will be part of our Quality Control team, responsible for a variety of activities including immunoassay testing on automated and semi-automated platforms, advanced data analysis, and prioritization and coordination and new product launch readiness in accordance with current Good Laboratory Practices (cGLPs). Key Responsibilities: Perform QC testing of incoming consumables and raw materials per compendial and non-compendial methods for GMP use in manufacturing. etc. | 4/21/2020 |
| 11522 | Qiagen Germantown, MD Contract Technical Associate - Kit Assembly Operations HS diploma or equivalent Exp: 1-3 year(s) |
Position Description: The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. Responsible for Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. Assist in the setup and preparation of required production related materials. etc. | 4/21/2020 |
| 11523 | Pyramid Laboratories Costa Mesa, CA Labeling and Packaging Technician BS/BA Exp: 1 year |
Under general supervision and instructions, responsible for the labeling and packaging of pharmaceutical products following cGMP, and Safety standards while maintaining a teamwork attitude to effectively manage production needs and meet the production schedule. PRINCIPAL DUTIES: Perform printing, labeling and final packaging execution activities as assigned per appropriate procedures using appropriate automated systems in place with a focus on quality and efficiency. etc. | 4/21/2020 |
| 11524 | Applied Medical Technologies Brecksville, OH Order Puller/Packer- 1st Shift HS Diploma/GED Exp: No experience necessary |
Process work orders by filling orders with raw materials for production floor. Package finished goods for shipment. Unload raw materials from truck. Responsible for quality control. No damaged product is sent out. No damaged raw material is accepted in. | 4/19/2020 |
| 11525 | Applied Molecular Transport South San Francisco, CA Research Associate BS or mS in biological/chemical sciences Exp: 1-5 years |
Applied Molecular Transport, Inc. is looking to hire a research associate in analytical method development and quality control (AD & QC) for its therapeutic programs. Perform analytical method development for LC based assays such as SEC, IEX and reversed-phase HPLC, and other protein-based analysis (i.e. SDS-PAGE, western blot, A280). Provide testing support for the in-house manufacture of drug substance and drug product. Execute stability studies to evaluate and characterize protein degradation during storage | 4/19/2020 |
| 11526 | Arbor Biosciences Ann Arbor, MI Resarch Associate - Next Generation Sequencing BS/BA in related field Exp: 1 year in molecular biology |
Routine activities of this role will involve evaluating client-provided DNA/RNA samples, converting them to NGS sequencing libraries, enriching them with hybridization probes, and amplifying them with PCR. Research & development activities using the same skills are also common. Fundamental understanding of the concepts and methods of PCR, ligation and other enzymatic reactions, strong laboratory skills, organizational skills, note-taking diligence, and attention to detail are key. | 4/19/2020 |
| 11527 | ArcherDX Boulder , CO Quality Control Associate I BS/BA in sciences Exp: 0-2 years in lab |
Evaluates and implements protocols and methods to inspect and test raw materials, in-process materials and finished products to ensure that they are in compliance with internal safety and quality standards for distribution as a Research Use Only (RUO) In-Vitro Diagnostic. Performs analysis and identifies trends in QC data and recommends corrective actions when necessary. Develops processes and tests with LEAN concepts in mind to determine that appropriate quality control analysis is being performed. | 4/19/2020 |
| 11528 | ArcherDX Boulder , CO Quality Assurance Specialist I/II BS/BA in sciences Exp: 1-3 years in quality role |
The Quality Assurance Specialist will provide support in the quality system area of Change Control Additionally, the Quality Assurance Specialist may provide support to one or more additional quality system area(s). Provide support for the maintenance of the change control management program. Assist with internal and external audit activities. Assist with management of Nonconformance Reports, Temporary Deviations, and Corrective and Preventive Action Reports, as applicable. | 4/19/2020 |
| 11529 | ArcherDX Boulder , CO Manufacturing Associate I BS/BA in sciences Exp: 1-2 years in FDA regulated manufacturing experience |
Associate level position for manufacturing medical devices in accordance with controlled procedures (SOPs) in compliance with Good Manufacturing Practice (GMP) regulations and current GMP (cGMP) guidelines. Manufactures solutions, labels and fills containers, labels and assembles kits. Compiles auditable electronic or paper records of manufacturing, maintains equipment logs and monitors supplies. | 4/19/2020 |
| 11530 | ArcherDX Boulder , CO Facilities Assistant HS Diploma/GED Exp: Previous facilities experience preferred |
The facilities assistant will be responsible for maintaining daily operations of the facility. The position will support facilities staff by preforming Facility maintenance duties such as furniture moves, simple electric projects, spot painting and/or cleaning, light constructions and exterior cleanup. The facilities assistant will also work with outside contractors on building and equipment repairs. | 4/19/2020 |
| 11531 | Arcus Biosciences Hayward, CA Bioanalysis Research Associate BS/MS in chemistry/biochemistry Exp: 1-4 years |
Arcus Biosciences is seeking a highly motivated and team-oriented candidate for the position of Research Associate in the Drug Metabolism and Pharmocokinetics (DMPK) Department. Develop, troubleshoot, and validate LC-MS/MS based bioanalytical methods. Analyze, summarize and report preclinical pharmacokinetic and toxicokinetic results | 4/19/2020 |
| 11532 | Arcus Biosciences Hayward, CA Research Associate/Sr. Research Associate BS/BA in biology, immunology or related Exp: 1-2 years research experience |
The role will be responsible for executing a variety of experiments including handling and analysis of ex vivo samples as well as performing in vitro assays to understand mechanism of action and pharmacodynamic properties of drug candidates. A successful candidate will contribute as part of a multidisciplinary team in a fast-paced environment to plan and execute experiments and subsequently collate, document, interpret, and present data internally. | 4/19/2020 |
| 11533 | Ardelyx Fremont, CA Quality Assurance Specialist I-III BS/BA or higher in sciences Exp: 1-7 years in manufacturing |
The QA Specialist I-III will provide QA support for Quality Operations and Quality System management. Working in a fast -paced pharmaceutical environment with a broad scope of responsibilities, the candidate will be able to bring many different skills to the job, with a focus on QA activities. The position requires diverse skill sets and will provide the opportunity to challenge an individual’s abilities to perform batch records review, data review and product dispositions, to implement sound Quality System improvements and manage QA procedures, assess GMP suppliers and service providers, and perform QA oversight of contract manufacturers. | 4/19/2020 |
| 11534 | Ardelyx Fremont, CA QA Specialist I - III BS in technical discipline/science/engineering Exp: 1-7 years in quality environment |
This role will be responsible for QA oversight of all GxP Computer Systems Validation. The incumbent, working with the functional teams must ensure that all GxP regulated systems are purchased, audited, installed and maintained based on industry best practices (e.g. GAMP5) and regulatory requirements (e.g. 21CFR Part 11 and relevant FDA Guidance). The position plans and organizes all QA activities for computer system validation projects. | 4/19/2020 |
| 11535 | Argonaut Manufacturing Carlsbad, CA Quality Control Assistant BS/BA in life sciences Exp: 1-2 years in GMP QC |
The purpose of this position is to provide support services by means of executing the analysis of in-process, finished product, and stability test samples. Further support services include Environmental Monitoring and Raw Material receipt activities. QC personnel are responsible for compliance with QC policies and procedures within the QC laboratory, company policies, and cGMP guidelines. This position will report to the Director, Quality Control. | 4/19/2020 |
| 11536 | Arrakis Therapeutics Waltham, MA Research Associate, Biophysics and Assay Development BS in biochemical sciences/chemistry Exp: 0-1 years in research |
The position requires good working knowledge of binding, thermodynamics and equilibrium, and kinetics. Contribute to screening of small-molecule and RNA interactions by SPR, MST, FP, and other assays as needed. Be motivated to independently analyze and report data from 100-1000s of small molecule candidates on a routine basis and report progress to team. | 4/19/2020 |
| 11537 | Pfizer Sanford, NC Bioprocess Technician BPT IV BS/BA Exp: 0 years |
The incumbent is a skilled manufacturing technician/operator with knowledge of microbial Fermentation, Purification, Chemistry and Process Support processes in the production of microbial vaccines and bulk intermediates. The incumbent is knowledgeable of required processing unit operations and control systems needed for operations. The incumbent performs scientific and operational tasks related to commercial manufacturing. The incumbent is a skilled manufacturing technician/operator with knowledge of microbial Fermentation, Purification, Chemistry and Process Support processes in the production of microbial vaccines and bulk intermediates. The incumbent is knowledgeable of required processing unit operations and control systems needed for operations. The incumbent performs scientific and operational tasks related to commercial manufacturing. | 4/19/2020 |
| 11538 | Pfizer McPherson, KA Chemist I - AB2 shift/12 hour night schedule BS in chemistry/biochemistry Exp: 0-1 years in lab |
Performs chemical analysis on purchased raw materials, in-process preparations, pure drug substances and finished pharmaceutical products to determine that they meet official compendial and/or Pfizer requirements. Perform standard qualitative and quantitative analysis on purchased raw materials, in-process products, pure drug substances, finished pharmaceutical preparations, stability samples, and contract manufacturing samples utilizing accepted gravimetric and spectrophotometric procedures, in accordance with approved testing procedures Pfizer, the National Formulary (NF), and the United States Pharmacopeia (USP). | 4/19/2020 |
| 11539 | Pfizer Lake Forest, IL CQ Lab Analyst BS/BA in sciences (chemistry or biology Exp: 0-1 years in QC or R&D |
The primary responsibility of this role includes using Functional/Technical skills to perform analytical testing and data processing in accordance with procedure, regulatory guidelines (FDA, MHRA, TGA, ICH, and DEA). This individual will need to seize accountability by assuring accurate laboratory records are kept in accordance with procedures and cGMPs. This individual will also be required to perform peer review of other’s laboratory solution notebooks. | 4/19/2020 |
| 11540 | Pfizer Sanford, NC Bioprocess Technician IV (Gene Therapy) BS/BA Exp: 0-2 years |
The incumbent is a skilled manufacturing technician/operator with knowledge of any of the following: solution preparation, upstream processing, downstream processing and Drug Product filling. The incumbent is knowledgeable of required processing unit operations and control systems needed for operations. The incumbent performs scientific and operational tasks related to commercial manufacturing. | 4/19/2020 |
| 11541 | Arraystar Rockville, MD Lab Assistant - Molecular Biology BS/BA in biological sciences Exp: 1-2 years wet lab experience |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. | 4/19/2020 |
| 11542 | Arrowhead Pharmacueticals Madison, WI Associate Chemist, Bioconjugation BS or MS in chemistry/biochemistry Exp: 1-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Scientist to join the Chemistry Department. The successful candidate will primarily focus on bioconjugation, analytical chemistry, formulation, and some small molecule organic synthesis. Perform bioconjugation, purification, and characterization of oligonucleotide conjugates. Identify critical issues/steps in a conjugation and solve the problems in a timely fashion | 4/19/2020 |
| 11543 | Arbor Biotechnologies Cambridge, MA Software Engineer - Research MS in engineering Exp: 1-2 years in industry |
At Arbor, you will be at the cutting edge of biodiscovery, systematically searching through nature’s diversity to discover and engineer new technologies for improving human health and sustainability. As a Software Engineer in Research, you will focus on building a search engine from the ground up. You will have significant latitude towards ideation, problem definition, and finding novel uses of machine learning. | 4/19/2020 |
| 11544 | AMPAC Fine Chemicals Rancho Cordova, CA Process Engineer I BS in chemical engineering Exp: 1-3 years in manufacturing |
Under general supervision and following established policies, performs professional assignments requiring full use and application of standard engineering principles, theories, concepts and techniques. Monitor existing processes, ensuring that batch records are maintained, variances are investigated, and day to day activities are properly planned. Activate and qualify facilities and equipment. | 4/18/2020 |
| 11545 | AMPAC Fine Chemicals Rancho Cordova, CA Analytical Scientist I BS in chemistry or related Exp: 1-3 years in method development/transfer |
Candidate will develop and validate methods; provide analytical support to the research and development group to meet project goals; select appropriate methods and techniques in performing experiments; collaborate with analytical personnel to help develop routine analytical methods; work cross functionally to achieve target goals and proactively seek out potential solutions to issues. Candidate will also assist in creating method validation and/or qualification protocols and reports as well as analytical methods;perform all lab work that will support method validation, transfer, and qualification; perform qualification of primary and secondary reference material to be used as analytical standards. | 4/18/2020 |
| 11546 | AMPAC Fine Chemicals Rancho Cordova, CA Operations Technician 1 HS Diploma/GED Exp: 1-4 years in chemical processing plant |
Operations Technician I will perform multiple duties related to the production of chemicals using a series if chemical processes in a batch type or continuous process chemical plant. These duties require careful observation and recording of data during all steps of the process. Assists in assigning tasks to other technicians, monitors performance of personnel, ensures that personnel follow all departmental and AFC policies and procedures, interacts with other personnel of other disciplines, participates in training fellow employees, conveys and logs status of processes, facilities, and personnel to the Crew Chief. Performs a variety of assignments in order to control process and equipment, both manually and with computers. Weigh, measure, and charge into chemical processing equipment a wide variety of chemicals. Operates all process equipment per operating instructions and procedures. | 4/18/2020 |
| 11547 | AMRI Albany, NY Research Scientist I BS/BA or MS in chemistry or related Exp: 0-5 years in medical chemistry |
The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. Purify synthesized chemicals to an appropriate degree. The scientist will be able to use the full range of chromatographic, crystallization, and distillation techniques. Analyze and identify compounds using a good range of modern separation and spectroscopic techniques. This will include interpretation of TLC, HPLC, polarimetry, IR, and NMR spectra of moderate complexity. | 4/18/2020 |
| 11548 | AMRI Springfield, MO Pilot Plant Technician HS Diploma/GED, BS/BA in chemistry preferred Exp: 0-2 years |
Set up and operate equipment to prescribed instructions to perform various unit operations such as reactions, filtrations, distillations, drying, milling, etc on raw materials and various stages of chemical processing. Follow and document per batch sheet instructions to produce products according to all current Good Manufacturing Procedure guidelines as required. | 4/18/2020 |
| 11549 | AMRI Grafton, WI QUALITY CONTROL ANALYST I BS/BA in chemistry or natural sciences Exp: 1-3 years in QC lab |
Conduct testing using approved analytical methods. Apply established laboratory methods or techniques to analysis, develop solutions to problems. Contribute to technical reports by providing detailed experimental write-ups. Maintain up-to-date laboratory records in accordance with company guidelines. Clearly document research and results in laboratory notebooks so that others can readily reproduce work. | 4/18/2020 |
| 11550 | AMRI Albany, NY Research Scientist I (Small Scale Manufacturing) BS in chemistry or related Exp: 0-2 years |
Adapt internal or customer supplied procedures to cGMP production operations. Manufacture batches of API, under cGMP protocols, for use in human clinical trials. Manage all aspects of a cGMP manufacturing campaign, including batch record review, safety evaluations, material procurement, equipment ordering/set-up/cleaning and project execution. | 4/18/2020 |
| 11551 | AMRI Lebanon, NJ Quality Control Analyst I BS/BA in engineering Exp: 0-2 years |
Assist with developing and validating test methods based on relevant ISO, ASTM standards and or client requirements. Independently perform tests per ISO, ASTM, and/or client requirements. Perform testing within the specified test plan and/or SOP for each test. Monitor projects for conformance with applicable SOPs and test specifications. | 4/18/2020 |
| 11552 | ARL Bio Pharma Oklahoma City, OK Chemist I-Analytical BS/BA in chemistry or related Exp: 0-2 years industrial experience |
Under general supervision, the Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine | 4/18/2020 |
| 11553 | AnaptysBio San Diego, CA Research Associate II MS/MA in molecular biology or related Exp: 0-2 years |
This position is responsible for cloning and expressing antigens, antibodies and their variants for our antibody discovery programs. Perform cloning methods, PCR methodologies, and vector and primer design. Perform PCR, DNA mini-, midi-, maxi-prepping procedures. Prepare and process samples for next generation sequencing. | 4/18/2020 |
| 11554 | Angiex Cambridage, MA Research Associate – Biology MS in biological/health sciences Exp: 1-3 years in lab |
Angiex is seeking a talented, creative, self-motivated research associate to join in (1) cell biology investigations of novel cellular pathways in endothelial cells and tumor cells, and (2) the evaluation of drugs specific to those pathways in cells in vitro and mice in vivo. | 4/18/2020 |
| 11555 | AngioDynamics Marlborough, MA Regulatory Affairs Specialist I BS in sciences/technical field Exp: 1+ years in regulatory affiars |
Responsible for determining the path to market for new and modifications to existing products in compliance with Regulations of intended market territory and for guiding teams on the required deliverables to support the Regulatory status of products distributed by AngioDynamics Inc. Under minimal supervision, acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, clarification and follow up of submissions under review | 4/18/2020 |
| 11556 | Anika Sarasota, FL IT Support Specialist BS/BA in computer science preferred, HS Diploma minimum Exp: 1-3 years in end-user management role |
The position is primarily responsible to provide local and remote hardware and software support for desktops, laptops, printers, and other peripherals. This position interacts with all levels of employees and candidates must be able to maintain a courteous, professional manner. Provide hardware and software support for all desktop, laptop, and other mobile users, to established standards and IT Service Level Agreement | 4/18/2020 |
| 11557 | Aphena Easton, MD Machine Operator- 2nd Shift (Night Shift) HS Diploma/GED Exp: 1 year in machine operation |
Change material rolls of various sizes. Clean and maintain ink printers. Change gears, sprockets and chains. Maintain jaws and replace tape as needed. Etc | 4/18/2020 |
| 11558 | Aveva Miramar, FL Engineering Technician BS/BA Exp: 0-3 years |
This person is responsible for the installation of new equipment including mechanical assembly and electrical, pneumatic, and thermal control fluid connections. Oversee and verify all operating aspects of new equipment at installation. Utilize detailed knowledge of mechanical components along with general knowledge of electrical equipment and controls, pneumatics, hydraulics, and plumbing to assemble and setup equipment. | 4/18/2020 |
| 11559 | Aveva Miramar, FL Manufacturing Operator I HS Diploma/GED Exp: 1-3 months |
Assists in the manufacturing of Aveva’s transdermal products.Coats blends and adhesives to produce laminate.Prepares finished and slit laminate rolls.Documents operational parameters for manufacturing equipment. | 4/18/2020 |
| 11560 | Aveva Richmond Hill, ON Lab Assistant, Microbiology (10 Month Contract) Associates or BS/BA Exp: 0-2 years |
Responsible for maintaining a constant inventory of clean laboratory glassware and a clean wash up area. Preparation of sanitizing and cleaning agents. Support of Microbiology laboratory, as required, in autoclaving of waste and preparation of microbiological media as per current procedures. Check glassware for cleanliness prior to restocking clean, dry glassware in storage areas in laboratory. Maintain a constant inventory of clean glassware and cleaning supplies. | 4/18/2020 |
| 11561 | Applied Medical Rancho Santa Margarita, CA CNC Machine Operations Engineer BS/BA in mechanical, industrial, manufacturing engineering Exp: 1-2 years in engineering |
As a CNC Machine Operations Engineer, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. Develop and sustain manufacturing processes. Debug manufacturing processes and equipment via root cause analysis. Develop and update engineering documents such as process maps, process FMEA, Manufacturing/Quality Instructions, test methods, drawings, and test reports | 4/18/2020 |
| 11562 | Applied Medical Rancho Santa Margarita, CA Associate Engineer Associates in engineering or sciences Exp: 1 year in engineering |
As an Associate Engineer, you will be responsible for working within the framework of a team and performing the following activities: Develop and update engineering documents such as manufacturing instructions, drawings and test procedures. Review and evaluate non-conforming materials, address customer experience reports, perform root cause analysis, and propose corrective/preventive actions. | 4/18/2020 |
| 11563 | Applied Medical Rancho Santa Margarita, CA Mechanical Engineer - Packaging BS in mechanical engineering Exp: 1 year in engineering |
As a Mechanical Engineer- Packaging you will be responsible for working within the framework of a team and performing the following activities: Design of product packaging and automated equipment using custom or off the shelf machinery to improve existing manufacturing processes. Generate documentation such as drawings, test protocols, reports, and troubleshooting guides, manufacturing instructions | 4/18/2020 |
| 11564 | Applied Medical Rancho Santa Margarita, CA Quality Engineer II BS/BA in engineering/STEM Exp: 1-2 years work experience |
As a Quality Engineer II, you will use your skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. Conduct experiments to prove hypotheses. Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques. | 4/18/2020 |
| 11565 | Ani Pharmaceuticals Baudette, MN Operator I - Production (1st, 2nd and 3rd Shift) HS Diploma/GED Exp: 1-2 years |
Assists in material handling, equipment set-up and breakdowns, documents process according to Master Production Records, and works with trained operators at assigned work centers to learn all aspects of the position, including batch record documentation, equipment set-up, operation and clean up. | 4/18/2020 |
| 11566 | Ani Pharmaceuticals Baudette, MN QC Chemist BS/BA in biological sciences or chemistry Exp: 1-3 years |
Perform review of data collected under approved test methods and investigational plans and protocols, in accordance with governing SOPs. Provide accurate assessment of data integrity, and document findings. Perform calibrations, preventive maintenance and repairs as needed on instrumentation. Qualify new equipment as assigned. Perform cGMP tasks such as laboratory housekeeping, auditing documentation and ordering supplies. Perform other duties as assigned or requested. | 4/18/2020 |
| 11567 | ARL Bio Pharma Oklahoma City, OK Research & Development Scientist I BS/BA in chemistry or related Exp: 0-2 years industrial experience |
The position requires the performance of variety of task including development and validation of analytical methods and qualitatively/quantitatively testing routine and non-routine client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation (HPLC/IC) used in a chemistry laboratory. | 4/18/2020 |
| 11568 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Chemistry Lab Associates or BS/BA in chemistry Exp: 0-2 years |
This position is responsible for maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position is responsible for the daily calibration and/or verification of the balances and pH meter. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform limited tests under supervision. | 4/18/2020 |
| 11569 | Amphastar Pharma Inland Empire, CA Machinist 1 year certification from college/tech school Exp: 0-4 years |
Sets up and operates conventional, special purpose, and numerical control (NC) machines and machining centers to fabricate metallic and nonmetallic parts by performing the following duties. Studies blueprints, sketches, drawings, manuals, specifications, or sample part to determine dimensions and tolerances of finished work-piece, sequence of operations, and setup requirements. | 4/18/2020 |
| 11570 | Amphastar Pharma Rancho Cucamonga, CA Validation Technician BS required Exp: 0-4 years |
Validates and maintains validation records of pharmaceutical product manufacturing equipment and processes by performing the following duties. Performs validations on equipment and process such as autoclaves, ovens, aseptic processes, product assembly lines, filling machines, sterilization processes, and cleaning process. | 4/18/2020 |
| 11571 | Aphena Cookeville, TN Facilities Maintenance Technician HS Diploma/GED Exp: 1-2 years in facilities maintenance |
Coordinate with other departments and team members for preventive maintenance work and repairs. Record and fill out work orders in accordance to company’s policy. Perform basic electrical work (replacing outlets, switches, light bulbs, ballast, light fixtures, reset breakers, etc.). Perform preventive maintenance program tasks related to facilities and plant services | 4/18/2020 |
| 11572 | Aphena Cookeville, TN Production Technician HS Diploma/GED Exp: 0-1 years in manufacturing |
Read and understand labels and batch records. Visual and Physical Checks on Product and Machine. Ensure compliance with all approved standard operating procedures based on regulatory and internal requirements. Review batch records to examine potential for corrective action | 4/18/2020 |
| 11573 | PAR Pharmaceutical Rochester, MI Quality Technician I, Chemistry HS diploma or equivalent Exp: 0-1 year(s) |
Responsible for laboratory and equipment cleanliness, routine physical testing per SOPs, and for receiving, stocking and inventorying reagents and supplies. Works with metrology to perform routine daily instrument calibrations and maintenance. Disposes of laboratory materials in accordance with EH&S, DEA and biohazard procedures. Communicates with the supervisor on a daily basis regarding the lab operations. Uses computer/lab software to enter the data. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. ROLE AND RESPONSIBILITIES: General Lab Support: Maintains the cleanliness of glassware by operating glassware washers or hand washing. Maintains laboratory and instrumentation organization and cleanliness. etc. | 4/15/2020 |
| 11574 | Catalent (Paradigm Diagnostics) Gaithersburg, MD Manufacturing Associate II BS in a scientific or engineering field Exp: 1-3 year(s) |
The Manufacturing Associate II is responsible for supporting the overall GMP manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II & commercial GMP manufacturing. The Role: Completes Batch Production Records under cGMP, and documents in detail through the use of SOPs and BPRs for the processes and manufacturing steps. Support initiation and closure of deviations; may serve as the lead in the departmental investigation and be responsible for closing out deviations and CAPAs. etc. | 4/15/2020 |
| 11575 | Catalent (Paradigm Diagnostics) Harmans, MD Manufacturing Associate II, Upstream BS in a scientific or engineering field Exp: 1-3 year(s) |
The Manufacturing Associate II, Upstream is responsible for supporting the overall GMP manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II & commercial GMP manufacturing. The Manufacturing Associate II Upstream role is critical to our patients. Manufacturing life-saving medicines right the first time for themselves and their team with patient safety in mind is our priority. Quality, safety and on-time delivery is a must to be successful in this role! etc. | 4/15/2020 |
| 11576 | Catalent (Paradigm Diagnostics) Baltimore, MD Manufacturing Associate I BS/BA Exp: 0-1 year(s) |
The Manufacturing Associate I perform and documents cGMP activities to support upstream or downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed. The Manufacturing Associate I is critical to our patients. Manufacturing life-saving medicines right the first time with patient safety in mind is our priority. Quality, safety and on-time delivery is a must to be successful in this role! etc. | 4/15/2020 |
| 11577 | Catalent (Paradigm Diagnostics) Rockville, MD Associate Scientist II - Analytical Development MS Exp: 0+ years |
The Associate Scientist II, Analytical Development will be responsible for process and product development within a dynamic project team. The ideal candidate will demonstrate strong technical knowledge, initiative, and scientific commitment, and make significant scientific and technical contributions within the Analytical Development Group as well as their project teams. The Associate Scientist, II Analytical Development role is critical to our patients. We generate high-quality tests/assays to provide patients with the best materials possible, with patient safety in mind, executing with efficiency always. Quality, safety, and on-time delivery is a must to be successful in this role! etc. | 4/15/2020 |
| 11578 | Catalent (Paradigm Diagnostics) Bloomington, IN Manufacturing Associate AS/AA Exp: 0-2 years |
A manufacturing associate’s primary duty is to perform variety of operational tasks in accordance with current GMP’s. Responsibilities include: Follow accurately all GMP documents (Batch records, SOP’s. Protocols, etc.), safely operate production equipment, operate in a clean room environment within required gowning, aseptic behaviors, and proper flow procedures, must work effectively in a team environment to achieve company goals, must adhere to company compliance, safety and attendance required. etc. | 4/15/2020 |
| 11579 | Catalent (Paradigm Diagnostics) Bloomington, IN Associate Manufacturing Technology Specialist BS/MS in a scientific or engineering field Exp: 0+ years |
The Role: Provide technical training as necessary to operators. Provide on-the-floor oversight of the manufacturing process, as necessary. Interact with client technical representatives, including Person in Plant observers on manufacturing floor. Monitor process data, identify trends, present data, and propose action as necessary. Perform technical troubleshooting and investigations of process issues. This includes documenting formal deviation investigations as needed. etc. | 4/15/2020 |
| 11580 | Catalent (Paradigm Diagnostics) Woodstock, IL Production Associate II - B Shift HS diploma or equivalent Exp: 1+ year(s) |
The position is responsible for packaging and inspecting pharmaceutical products in accordance with packaging instructions, Standard Operating Procedures (SOP), and current Good Manufacturing Practices (cGMP) while adhering to health and safety requirements. The Production Associate II role is critical to our patients. They oversee all inspection of our products with safety in mind, executing with efficiency always. The Role: Monitor and direct employee position rotations on the line. Assist team lead in the coordination of OJT. etc. | 4/15/2020 |
| 11581 | Paragon Genomics Hayward, CA Quality Assurance Specialist BS in molecular biology, chemistry, or other life science Exp: 1+ year(s) |
We are seeking a Quality Assurance (QA) Specialist that can build out and implement a Quality Management System (QMS) from the ground up, focusing initially on ISO 9001 certification and transitioning to ISO 13485 certification. The QA Specialist ensures compliance with policies and procedures, serves as the main point of contact for customer quality audits and provides quality system performance reports to management. This position will be expected to take a hands-on approach to activities in production and other processes, in order to identify and recommend opportunities for improvement. etc. | 4/15/2020 |
| 11582 | Paraxel Durham, NC Software Developer BS in computer science or related Exp: 1 year |
Parexel is hiring an Associate Software Engineer to play a key role in the implementation of COTS applications as well as design, development, testing and maintenance of the clinical applications. The Associate Software Engineer will be expected to provide a solution to business requirements with offering functional design and implementation. Associate Software Engineer also collaborates with peers, product owner, Scrum master to deliver releases in agile development practice. etc. | 4/15/2020 |
| 11583 | PBS Biotech Camarillo, CA Research Associate, BioprocessR&D MS in chemical or biochemical engineering, or a life science Exp: Not necessary for MS candidates |
We are seeking a full-time, highly motivated Research Associate to join our growing bioprocess R&D team. This position is an invaluable opportunity to gain experience working with cutting edge technology and a variety of cell types that are significant to the rapidly emerging cell and gene therapy market. Responsibilities and Tasks: Participate in research efforts for various cell culture processes based on client needs. Perform experiments for bioprocess development, optimization, and characterization. Prepare scientific data for external publications, abstracts, and presentations, including those at international conferences and trade shows. Support root-cause analysis for unexpected results and provide new approaches or experimental strategies for problem solving. etc. | 4/15/2020 |
| 11584 | PCI Sequens Research Devens, MA Process Chemist R&D BS/MS in chemistry Exp: 0-5 years |
The successful candidate is expected to be able to participate in a chemical synthesis program with the objective to develop a chemical process that can be safely performed on large scale. This involves being able to design, adapt and execute synthetic procedures and purification methods on a laboratory scale to fit the requirements of the development or scale-up plant. etc. | 4/15/2020 |
| 11585 | New England Peptide Gardner, MA Lab Assistant Unspecified Exp: 0-1 year(s) |
NEP is seeking a highly motivated individual interested in a career in the Biotech/Pharmaceutical industry. Local candidates only. No experience necessary, we will train! Working alongside other Peptide Scientists and Technicians, the Lab Assistant will help support the production process. Job duties may include: Weighing of Amino Acids. Stocking Chemicals. etc. | 4/15/2020 |
| 11586 | New England Peptide Gardner, MA Lab Assistant (Night Shift) Unspecified Exp: 0-1 year(s) |
NEP is seeking a highly motivated individual interested in a career in the Biotech/Pharmaceutical industry. Local candidates only. No experience necessary, we will train! Working alongside other Peptide Scientists and Technicians, the Lab Assistant will help support the production process. Job duties may include: Weighing of Amino Acids. Stocking Chemicals. etc. | 4/15/2020 |
| 11587 | New England Peptide Gardner, MA Lab Technician BS in biology, chemistry, or related Exp: 1 year |
NEP is seeking a qualified individual interested in a career in the Biotech/Pharmaceutical industry. Working alongside other peptide scientists, the Lab Technician will be responsible for synthesizing, analyzing and purifying peptides. This is an excellent opportunity to get practical, hands on experience at a thriving biotech company. etc. | 4/15/2020 |
| 11588 | New England Peptide Gardner, MA Lab Technician (Night Shift) BS in biology, chemistry, or related Exp: 2 year |
NEP is seeking a qualified individual interested in a career in the Biotech/Pharmaceutical industry. Working alongside other peptide scientists, the Lab Technician will be responsible for synthesizing, analyzing and purifying peptides. This is an excellent opportunity to get practical, hands on experience at a thriving biotech company. etc. | 4/15/2020 |
| 11589 | Personalis Menlo Park, CA Business Development Associate BS in a life science Exp: 1-2 year(s) |
The Business Development Associate will be primarily responsible for developing and nurturing a pipeline of immuno-oncology and targeted therapy prospects in small to mid-size biotech/pharma globally. The Business Development Associate manages inquiries by phone and/or web, identifies target accounts decision makers, sets up appointments for corporate field sales and reports results on each. Will be required to proactively initiate and manage cold call activities into a target list of accounts, warm calls from trade show and other incoming lead sources. The Business Development Associate must be able to identify and qualify opportunities, build trust and credibility, deliver a clear and compelling message, uncover initiatives and gain commitment from prospect to engage with Personalis. etc. | 4/15/2020 |
| 11590 | Personalis Menlo Park, CA Laboratory Assistant BS in molecular biology or related Exp: 0-2 years |
We are looking for a team-oriented Laboratory Assistant to join our operations team. The ideal individual must have the ability to think on their feet and troubleshoot issues. Within a dynamic startup environment, the successful candidate, under direction of the Laboratory management, will help grow the sequencing services laboratory. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. Responsibilities: Adhere to the laboratory's quality control policies. etc. | 4/15/2020 |
| 11591 | Personalis Menlo Park, CA Research Associate - Operations BA/BS in a biological discipline Exp: 0-2+ years |
Located in Menlo Park, CA, we are seeking a talented and highly motivated Research Associate to join our Operations Team. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. Responsibilities: Participates in a hands-on fashion to the daily lab activities in one of the following areas by performing and assisting in laboratory tests, processes and analyses according to the laboratory’s standard operating procedures. etc. | 4/15/2020 |
| 11592 | FCX Performance Plymouth, MI Instrument Technician HS diploma/AS in process instrumentation Exp: 1-3+ year(s) |
Essential Functions & Responsibilities: Respond to customer inquiries & requests to perform maintenance, repair, installation, and calibration on various types of high-end industrial electronic and standard instrumentation & measurement devices. Perform data collection and analysis of the various technologies; including but not limited to Vibration, Motor Circuit, Oil, and/or Power Quality Analysis. Report job activity as well as maintain detailed logs about service calls, parts, and orders. Identify opportunities for upgrades at the customer facility. etc. | 4/15/2020 |
| 11593 | Pharmaron Germantown, MD Laboratory Technician, Accelerator Mass Spectrometry BS/BA in related field Exp: 6-12 months |
We are looking for a Laboratory Technician to work on a full-time basis in our Germantown, MD facility. This position is responsible for carrying out sample analysis and data processing within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company Policies. Contributes to the laboratory and equipment maintenance to ensure efficient operations. Essential Functions: To work to the Company’s quality procedures in accordance with GLP and GCP regulations and be involved in working to and generating a culture of continuous improvement. To comply with the Company’s Health and Safety, MOSH and ionizing radiation procedures. To participate in the day‐to‐day operation of the Laboratory, the analysis of samples and associated duties. etc. | 4/15/2020 |
| 11594 | Pharmaron Germantown, MD Associate Bioanalytical Scientist, Large Molecule Bioanalysis BS/MS in related field Exp: 0-1+ year(s) |
This position is responsible for carrying out sample analysis and data processing within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company Policies. Contributes to the laboratory and equipment maintenance to ensure efficient operations. Essential Functions: Perform serological and cell-based LBA assays (ELISA/ECL) using plate readers, MSD and flow cytometry. Basic operation and routine maintenance of general laboratory equipment. Participate in day-to-day operation of the Laboratory, the analysis of samples and associated duties. Responsible for handling and processing of biological samples including competent handling and pipetting technique. etc. | 4/15/2020 |
| 11595 | Pharmaron Germantown, MD Associate Bioanalytical Scientist, Accelerator Mass Spectrometry BS/MS in related field Exp: 0-1+ year(s) |
This position is responsible for carrying out sample analysis and data processing within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company policies. Contributes to the laboratory and equipment maintenance to ensure efficient operations. Essential Functions: Participate in day-to-day operation of the Laboratory, the analysis of samples and associated duties. Responsible for handling and processing of biological samples including competent handling and pipetting technique. Prepare/review data tables and reports within Laboratory Information Management System (LIMS). etc. | 4/15/2020 |
| 11596 | PLDevelopments Copiague, NY Process Operator I – Copiague, NY HS diploma or equivalent Exp: 1 year |
POSITION RESPONSIBILITIES: Reports process or equipment problems to supervisor; performs general troubleshooting. Ensures batch records, equipment log books, and other relevant records are current; performs batch record reconciliation. Sets up and operates equipment for processing operations. Cleans and maintains processing rooms and equipment. Monitors process and equipment and makes necessary adjustments to maintain batch record specifications. etc. | 4/15/2020 |
| 11597 | Poseida Therapeutics San Diego, CA Lab Technician BS/BA Exp: 6 months+ |
Poseida is seeking an outstanding candidate to join our Research Operations team. The Lab Technician is responsible for providing broad support for research personnel by maintaining lab facilities, carrying out basic lab equipment maintenance, washing and autoclaving glassware, coordinate collection of biohazard/chemical waste, and replenishing lab supplies. Responsibilities: These may include but are not limited to: Set up and carry out daily operational maintenance of lab equipment, including incubators, water baths, biosafety cabinets, centrifuges, and cold storage units. etc. | 4/15/2020 |
| 11598 | Precision Biosciences Durham, NC Associate Process Engineer/Process Engineer, Downstream MS in chemical engineering, biological engineering, or relevant science Exp: 0-2 years |
Precision BioSciences is currently seeking to fill the role of Associate Process Engineer or Process Engineer. This position will be a critical part of the team charged with developing a world-class manufacturing process for making an mRNA-based active pharmaceutical ingredient (API). The candidate will participate in all aspects of process development, including in-vitro transcription, downstream purification and testing of products and intermediates. Responsibilities: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document. Set up and run transcription reactions at small and large scale. Assist in the development of downstream purification operations appropriate to the scale of the process. Collaborate with the Analytical team to perform in-process and final product testing. etc. | 4/15/2020 |
| 11599 | Precision Frederick, MD Processing Technician I/II - Biological Samples BS in biology, chemistry, or other life science Exp: 1-2 year(s) |
Our Processing Technician I receive and inventory all incoming fresh biological samples into LIMS database, perform cell isolations and/or separate whole blood and body fluids into various components, perform cryopreservation of all isolated cells, prepare reagents used in lab, perform cell thawing and counting, create and perform first key of data collection sheets. In addition to the above, the Processing Technician II perform plate based assays such kit based ELISAs for clinical patient specimen samples, QC analyses for controls and standards utilized in the plate based assays to ensure that results meet specifications, isolation and cryopreservation of intact RNA, miRNA and DNA from clinical patient specimen samples of all tissue and types, quantification and QC evaluation of nucleic acid samples including Picogreen assays and QC analyses (RNA/DNA integrity analysis, Real-Time PCR) to ensure that results meet specifications and perform equipment preventive maintenance. etc. | 4/15/2020 |
| 11600 | PRESCOS San Diego, CA Vivarium Assistant HS diploma or equivalent Exp: 0-1 year(s) |
We are looking for a full-time Vivarium Assistant to perform husbandry tasks such as the changing and cleaning of animal cages, feeding/watering of animals, and the sanitation/ cleaning of the animal facility. Essential functions: Perform cage changes (provide food/water and change bedding) and routine daily health monitoring. Washing and sterilizing of laboratory caging, supplies and equipments. Maintain and upkeep documentations such as animal cage cards, duty log sheets, animal computer database, and sanitation logs. etc. | 4/15/2020 |
| 11601 | Prevail New York, NY Lab Associate - Process Development MS Exp: 1-2 year(s) |
Reporting to the Director of Process Development, the Lab Associate of Process Development will play a critical role in our efforts to advance the development of AAV gene therapy pipeline drugs for neurodegenerative disorders. We are looking for an enthusiastic, self-motivated, hands-on lab associate with excellent interpersonal skills who is comfortable working in an open environment spanning multiple functions. As an early hire at a new company, you will have exposure to senior management, to all activities at Prevail, and you will be influential in championing and developing our culture. etc. | 4/15/2020 |
| 11602 | Propharma Group Montreal, QC Biologics Validation Engineer - Consultant BS/BA in a related field Exp: 1-10 year(s) |
Job Description: Preparing and executing validation documents in a biologics environment. Project execution for multiple systems validation. Understanding the hours budgeted for completion of each task on a specific. Individuals must represent the company and division at client sites and interact confidently with clients, contractors, management, and peers. Develop Installation, Operational and simple Performance qualification documents. etc. | 4/15/2020 |
| 11603 | ProSciento San Diego, CA Clinical Research Associate BS in a life science Exp: Not necessary for BS candidates |
Essential Duties and Responsibilities include the following. Other duties may be assigned at the Company’s sole discretion. Responsible for all aspects of study site monitoring including site qualification visits, pre-study visits, site initiation visits, routine monitoring visits, and close-out visits of clinical sites. Ensures the protection of study subjects by verifying that informed consent procedures have been followed and protocol requirements are adhered to according to applicable regulatory requirements. Monitors, tracks, and follows up on all Adverse Events (AEs) and Serious Adverse Events (SAEs). Ensures all SAEs are reported to sponsor and regulatory authorities within required timelines. | 4/15/2020 |
| 11604 | Promega Madison, WI Product Finishing IVD Technician 1 HS diploma or equivalent Exp: 1+ year(s) |
Technician with a full understanding of the department including dispensing, kitting and labels. Uses technical concepts and depth of knowledge to resolve issues effectively. ESSENTIAL DUTIES: Setup, operate and maintain manual and automated dispensing, capping and labeling equipment. Pull products from inventory and assemble components into kits and kit sub-assemblies using quality system documents, including kit packaging diagrams (KPDs). Accurately complete all required written documentation for batch records. etc. | 4/15/2020 |
| 11605 | Performance Validation Unspecified, IN Level 1 Staff Validation Engineer BS in mechanical, chemical, or biomedical engineering Exp: Entry level |
Performance Validation is seeking full-time Level 1 Validation Engineer/Specialists in the following locations: Indiana, Michigan, Illinois, and Kansas. The Level 1 Validation Engineer/Specialist is an entry level position and reports directly to the Division Director or Manager and is assigned to one or more project teams to perform work for Performance Validation’s customers. etc. | 4/15/2020 |
| 11606 | Performance Validation Unspecified, IN Level 1 Staff Validation Specialist BS in the life sciences Exp: Entry level |
Performance Validation is seeking full-time Level 1 Validation Engineer/Specialists in the following locations: Indiana, Michigan, Illinois, and Kansas. The Level 1 Validation Engineer/Specialist is an entry level position and reports directly to the Division Director or Manager and is assigned to one or more project teams to perform work for Performance Validation’s customers. etc. | 4/15/2020 |
| 11607 | PRA Health Sciences Charlottesville, VA Safety Assistant HS diploma/BA/BS Exp: 1-2 year(s) |
You’ve been working as a pharmacy, lab or medical technician and want to utilize your skills in a new environment that allows for long-term career growth opportunities. Or, as a new graduate or early-career professional, you’ve been wondering how to put your degree in biology, chemistry, or other life sciences to practice in a meaningful way. Are you incredibly detail-oriented to ensure the accuracy and reliability of your work? Do you want to impact the lives of others through research – helping to develop cutting edge, safe pharmaceuticals that will extend the life of or cure others? If so, you are an emerging drug safety professional! etc. | 4/15/2020 |
| 11608 | PRA Health Sciences Salt Lake City, UT Lab Associate PRN BS/BA in a medical, laboratory, or life science Exp: 1-2 year(s) |
The Lab Associate is part of the operational team within the sample preparation laboratory. The Lab Associate ensures the appropriate collection, processing, storage and shipment of samples. Daily tasks may involve maintenance of equipment, processing and shipment of samples. The Lab Associate is part of the study team that is responsible for the execution of the study. etc. | 4/15/2020 |
| 11609 | PRA Health Sciences Salt Lake City, UT Medical Research Associate FT Nights - Salt Lake City BS/BA in a clinical or health related area Exp: 1-2 year(s) |
Who are you? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you! Clinic Tasks: Screen potential subjects. Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability etc. | 4/15/2020 |
| 11610 | PRA Health Sciences Charlottesville, VA Safety Assistant 2 HS diploma/BA/BS Exp: 1-2 year(s) |
You’ve been working as a pharmacy, lab or medical technician and want to utilize your skills in a new environment that allows for long-term career growth opportunities. Or, as a new graduate or early-career professional, you’ve been wondering how to put your degree in biology, chemistry, or other life sciences to practice in a meaningful way. Are you incredibly detail-oriented to ensure the accuracy and reliability of your work? Do you want to impact the lives of others through research – helping to develop cutting edge, safe pharmaceuticals that will extend the life of or cure others? If so, you are an emerging drug safety professional! etc. | 4/15/2020 |
| 11611 | Poseida Therapeutics San Diego, CA Research Associate, Immuno-Oncology MS in immunology, molecular biology, or related Exp: 0+ years |
Poseida is seeking an outstanding candidate to join our immuno-oncology team. The Research Associate will support the development chimeric antigen receptors (CAR-T) cellular therapies against cancer and will involve bench work, laboratory studies, and the coordination of research projects with the assistance of a senior lab member and/or lab director. Responsibilities: These may include but are not limited to: Support the development of CAR-T cellular therapies. Studies may include work with molecular biology and cloning techniques, tissue culture of human cell lines, isolation of cells from blood products, virus production, in vitro human cell-based immunoassays, and cell separation techniques. etc. | 4/15/2020 |
| 11612 | Pharmaron Germantown, MD Associate Bioanalytical Scientist, Small Molecule Bioanalysis BS/MS in related field Exp: 0-1+ year(s) |
This position is responsible for carrying out sample analysis and data processing within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company policies. Contributes to the laboratory and equipment maintenance to ensure efficient operations. Essential Functions: Participate in day-to-day operation of the Laboratory, the analysis of samples and associated duties. Responsible for handling and processing of biological samples including competent handling and pipetting technique. Prepare/review data tables and reports within Laboratory Information Management System (LIMS) etc. | 4/15/2020 |
| 11613 | Nova Biomedical Waltham, MA Reagent Packager I HS diploma or equivalent Exp: 1+ year(s) |
The Packager, under general supervision, will follow established procedures in packaging reagent kits. This individual is responsible for working on an assembly line to assemble the various kits within the established quality and time standards. The individual will work with various packaging equipment such as: automated/manual tape machines, manual pallet trucks, conveyors, flow racks and other packaging devices. | 4/8/2020 |
| 11614 | Nova Biomedical Waltham, MA Chemical Filling Operator - First Shift Unspecified Exp: 0-2 years |
The Filling Operator is responsible for the proper filling, sealing and labeling of various reagents. Responsibilities include: monitoring and maintenance of the filling equipment during operation, recording necessary data into procedures, inspection of product, loading/unloading product from equipment and movement of materials. Requirements: High School Diploma or equivalent. Must be able to lift up to 50 pounds and be able to work alternately in a seated or standing procedure. Must have basic mechanical aptitude and the ability to read, write and comprehend English. Ability to wear cartridge type respirator. Will work with hand tools and gages to properly operate filling equipment such as bottle fillers and pouch fillers. Ability to operate electric and manual pallet jacks. Requires 0 to 2 years’ experience as a machine operator. Entry level knowledge of Quality System Regulations, Good Manufacturing Practices, and OSHA safety standards desirable. Hours: Monday – Friday, 6:45 AM – 3:15 PM. | 4/8/2020 |
| 11615 | Nova Biomedical Waltham, MA Replenishment Associate HS diploma Exp: 1 year |
The Receiving Replenishment Associate's is responsible for maintaining raw inventory within the raw material warehouse area. As part of the Receiving Team, the Replenishment Associate will be responsible for (1) the moving of raw material from the Receiving dock to the warehouse, (2) the consolidating of raw material in the warehouse, and (3) the picking and delivering of raw materials to the manufacturing floor. The Replenishment Associate will use documented procedures and good judgement to ensure inventory is stocked in an optimum manner, controlled, and ready for picking. Essential Responsibilities: Essential Responsibilities are to ensure the accurate movement (stocking, replenishing, consolidating, blocking, fulfilling) of materials and products within the Distribution Department and report any /all batch number or quantity discrepancies related to Distribution materials. Perform cycle counting of assigned materials / products, assist in reconciling variances, identify materials/ products with assigned placards (short-dated, Quality holds, etc.). etc. | 4/8/2020 |
| 11616 | Novo Nordisk Durham, NC Maintenance Technician (Packaging)- OFP AA/AS in a relevant field Exp: 1 year |
Position Purpose: Improve systems & equipment reliability on assigned process, reduce system/equipment downtime on assigned process & support operation of assigned process. Accountabilities: Follow all safety & environmental requirements in the performance of duties. Follow Standard Operating Procedures in performance of assigned duties. Support the development & establishment of maintenance procedures, maintenance plans & spare parts lists for processes assigned. Perform corrective & preventative maintenance on assigned process in a timely manner. etc. | 4/8/2020 |
| 11617 | Novo Nordisk West Lebanon, NH Quality Control Microbiologist I BS in a scientific discipline Exp: 0-2 years |
This position carries out routine microbiological testing to support the manufacturing facility. All work is carried out in a Quality Control (QC) Good Manufacturing Practice (GMP) environment where the highest level of compliance and attention to detail is necessary. Role focuses on routine activities such as utility and facility monitoring, data reporting, general laboratory support and activity coordination. This individual works with supervision/instruction on routine work and detailed instruction for new activities. Main Job Tasks: Duties include but are not limited to: Conducts routine microbiology assays following Standard Operating Procedures (SOP’s) such as bioburden and endotoxin testing. Collects Environmental Monitoring samples including high quality water systems, cleanroom environments and gases in the field (manufacturing, utilities and laboratory locations). etc. | 4/8/2020 |
| 11618 | Novo Nordisk West Lebanon, NH Facilities Equipment Technician AS/AA Exp: 1 year |
The Facilities Equipment Technician will be responsible for routine maintenance and troubleshooting of equipment – such as diaphragm valves, centrifugal pumps, pressure regulators, autoclaves, Clean in Place (CIP) systems, centrifuge, and homogenizer. This role will assist in the coordination and execution of manufacturing equipment maintenance, improvement programs, and quality responses for process equipment as needed. Main Job Tasks: Perform preventive maintenance (PM) of manufacturing related equipment. Perform trouble shooting, repair and corrective maintenance (CM) of manufacturing related equipment. etc. | 4/8/2020 |
| 11619 | Nuvasive Memphis, TN Associate Engineer, Quality BS in an engineering discipline Exp: 0-2 years |
This role is responsible for the, implementation, and improvement of overall quality systems. The Associate Quality Engineer will participate in Design Control activities and provide guidance to engineering on successful creation and maintenance of design history files during new product introductions. The Associate Quality Engineer may work closely with suppliers or contractors, including auditing, developing inspection/testing plans, performing risk analysis. Lead the development of adequate inspection criteria. Identify the need for custom gauging for NuVasive and suppliers. Identify and qualify equipment required to perform inspection. Support transfer of design to internal or contract manufacturing, including establishment of inspection plans both at NuVasive and at the supplier. Evaluate product and process changes for qualification and validation requirements and assist in change implementations. etc. | 4/8/2020 |
| 11620 | Nuvasive Aliso Viejo, CA Clean Room Technician Unspecified Exp: 1+ year(s) |
This role ensures that production is not contaminated by following strict clean room guidelines. Duties include knowing and following all clean room protocols, keeping work areas organized, and maintaining equipment. Key Responsibilities: Follow clean room procedures. Follow production schedule. Follow Instructions. Read drawings and Work Orders. Collect materials required. Assemble mechanical sub- and final assemblies according to QSR’s, Manufacturing Instructions (MIs), and other applicable company procedures. etc. | 4/8/2020 |
| 11621 | Nuvasive Memphis, TN Quality Technician Unspecified Exp: 1-3 year(s) |
The Quality Technician is responsible for performing on-site calibration activities and managing a calibration program. Primary duties include performing calibrations utilizing advanced inspection equipment such as a supermic or vision systems, generating controlled documents required to maintain compliance to standards for performing calibrations, contacting vendors for requesting return or calibrations of custom / functional gauging. Review/analyze data and documentation for Quality managed systems. An understanding of industry standard and advanced inspection equipment is necessary to perform essential job duties. etc. | 4/8/2020 |
| 11622 | Nuvasive West Carrollton, OH Production Associate - 2nd Shift HS diploma or equivalent Exp: <1 year |
The Associate Post Processing Technician is responsible for the finishing/assembly operations to ensure quality products are produced. The Post Processing Technician helps in driving best practices and creates open communication across all teams to foster a collaborative, high functioning culture. Understand setup and final assembly instructions. Process product through laser marking process with high accuracy and attention to detail. Follow standard applications in order to achieve dimensional integrity and required finish characteristics. Follow the router protocol to ensure the product moves through channels efficiently and GDP is correct prior to moving the product to the next area. Work from quality review and corrective work documents to repair or rework parts. etc. | 4/8/2020 |
| 11623 | Nuvasive Memphis, TN Associate Sterile Processing Tech HS diploma or equivalent Exp: 1+ year(s) |
Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties: Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in-process production reports, and status of material locations. etc. | 4/8/2020 |
| 11624 | Nuvasive West Carrollton, OH Production Associate HS diploma or equivalent Exp: 1-2 year(s) |
The Post Processing Technician is responsible for the finishing/assembly operations to ensure quality products are produced. The Post Processing Technician helps in driving best practices and creates open communication across all teams to foster a collaborative, high functioning culture. Understand setup and final assembly instructions. Process product through laser marking process with high accuracy and attention to detail. Follow standard applications in order to achieve dimensional integrity and required finish characteristics. Follow the router protocol to ensure the product moves through channels efficiently and GDP is correct prior to moving the product to the next area. Work from quality review and corrective work documents to repair or rework parts. etc. | 4/8/2020 |
| 11625 | Nuvasive Aliso Viejo, CA Manufacturing Technician Unspecified Exp: 1+ year(s) |
Job Description: Align, fit, and assemble component parts, using hand tools, power tools, fixtures, and templates. Analyze and record test results per acceptance test criteria, and prepare written testing documentation. Organize work areas. Install electrical and electronic parts and hardware in housings or assemblies, using soldering equipment and hand tools. Read blueprints, schematics, diagrams, manufacturing instructions, and work orders to determine methods and sequences of assembly. Repair, rework, and calibrate assemblies and systems to meet operational specifications and tolerances. Test performance of electromechanical assemblies, using test instruments such as oscilloscopes, and electronic voltmeters. etc. | 4/8/2020 |
| 11626 | Nuventra Pharma Sciences Durham, NC Regulatory Publishing Associate BS/BA Exp: 1-2 year(s) |
We seek an experienced eCTD publisher for a growing regulatory operations team. The ideal candidate will be self-motivated, detail-oriented, and will have eCTD publishing experience in both US and global markets. This is an office-based position in Durham, NC. Responsibilities: Use Microsoft Word and Adobe Acrobat to format and compile submission-ready documents. Build electronic (eCTD) regulatory submissions, including INDs, NDAs, and BLAs, utilizing industry-standard publishing software. Perform quality control reviews of submissions within publishing software. etc. | 4/8/2020 |
| 11627 | OraSure Technologies Bethlehem, PA Manufacturing Technician - 2nd Shift HS diploma or equivalent Exp: 0-2 years |
Operate equipment for the assembly of medical diagnostic tests. Schedule for this position will be Monday-Friday 3:30 PM-12 AM. Responsibilities: Operate semi-automated and automated equipment in the production area at a sufficient rate and quality level. Perform on-line inspection of all components/parts produced. Take corrective action and/or make recommendations to the supervisor. Complete all paperwork and equipment logbooks and review other operator's paperwork for accuracy and completeness as required. etc. | 4/8/2020 |
| 11628 | Organogenesis Norwood, MA Materials Handler HS diploma or equivalent Exp: 1 year |
KEY RESPONSIBILITIES: Receives and labels incoming materials. Delivers materials to internal customers. Produce labels for finished products. Product labeling and packaging. Assist in the daily scheduling of activities. Prepare and package outgoing product shipments. Print and prepare documentation. Complete cycle counts and inventory checks in a timely and accurate manner. etc. | 4/8/2020 |
| 11629 | PACT Pharma South San Francisco, CA Clinical Immunology Research Associate BS/MS Exp: 1+ year(s) |
We are currently recruiting for Research Associate in Clinical Immunology. This position will be based in South San Francisco. Who you are: A person eager to contribute to new understanding of T cell and cancer biology by preparing and analyzing samples from patients in our clinical trial. A detail-oriented person who takes pride in producing high-quality, accurate data. A person who prefers clear and consistent job responsibilities and objectives. etc. | 4/8/2020 |
| 11630 | PACT Pharma South San Francisco, CA Molecular Biologist Research Associate I / II MS Exp: 1+ year(s) |
The ideal candidate should be experienced in the latest molecular cloning techniques and in mammalian cell culture. The candidate should enjoy operating in an exceptionally dynamic and cooperative environment and will communicate results to and coordinate efforts with a larger cross-disciplinary team of immunologists, biologists, engineers and bio-informaticians. What you will do: The candidate will be generating plasmids expressing patient-derived T cell receptors using an established molecular cloning protocol. He/she will also be responsible for genome engineering human T cells to express the patient-derived T cell receptors. etc. | 4/8/2020 |
| 11631 | PACT Pharma South San Francisco, CA Research Associate BS/BA Exp: 0-2 years |
We are currently recruiting for a Research Associate who will report to the Scientist and continue advancing PACT’s cutting edge engineered cell product. This will be a unique opportunity to see your ideas rapidly translate into the clinic and impact patient lives. What you will do: Support the Protein Production pipeline with high-throughput DNA Prep, cloning, protein expression and purification. Expression and purification of recombinant proteins in mammalian host system. etc. | 4/8/2020 |
| 11632 | PACT Pharma South San Francisco, CA Research Associate Protein Sciences BS/BA Exp: 1-2 year(s) |
We are currently recruiting for a Research Associate Protein Sciences who will report to the Associate Director of Protein Sciences and continue advancing PACT’s cutting edge engineered cell product. This will be a unique opportunity to see your ideas rapidly translate into the clinic and impact patient lives. The individual will be responsible for the execution of high-throughput cloning, protein expression and purification and will be involved in the critical path for the discovery of neoEpitope and corresponding cognate TCRs. The position involves a considerable amount of bench work in a GMP-like environment and will on protocols and SOP executions to support our clinical trial. The ideal candidate should have keen attention to details, be highly organized and should enjoy operating in an exceptionally dynamic and collaborative environment. etc. | 4/8/2020 |
| 11633 | PAR Pharmaceutical Chestnut Ridge, NY Quality Associate l HS diploma or equivalent Exp: 0-1 year(s) |
The Quality Associate I, Operations is responsible for actively participating in “on the floor” Quality activities during product manufacturing and/or packaging. Quality activities include product sampling and inspection, area clearance to confirm process readiness, and non-conforming event support to resolve in-process issues. Communicates to multiple departments and supervision to provide timely process and issue updates. Identifies and escalates issues or problems to appropriate supervision. Participates as a team member on cross-functional teams. Participates in reviews and structured processes for continuous improvement. etc. | 4/8/2020 |
| 11634 | OraSure Technologies St. Paul, MN Software Engineer BS in computer science Exp: 6 months |
We are looking for a team member who can contribute to our high-throughput data tracking and analysis applications. We generate terabytes of genomic data per week and need to ensure efficient and accurate tracking is completed along with quick, accurate, and reproducible data analysis. By facilitating fast and easy data access for our clients, we expedite advances in scientific knowledge. Our new software engineer will join a development team of highly-motivated, passionate and inclusive engineers. If you’re looking for a position that will directly improve human health and the environment, we want you! etc. | 4/8/2020 |
| 11635 | OraSure Technologies Bethlehem, PA Quality Control Specialist I AS in chemistry, biology, medical technology or related Exp: 1 year |
Quality Control Specialist I personnel perform procedures that include evaluation of raw materials, in-process components, finished products, stability testing, equipment quality control, and equipment maintenance in compliance with guidelines established by Orasure Technologies and regulatory agencies. Responsibilities: Perform all procedures accurately and according to written Work Instructions and SOPS as indicated in the Quality Control procedures and other applicable facility procedures. Perform testing at all levels of production including raw materials, in-process components, finished products and stability testing. Perform visual finished product inspections. etc. | 4/8/2020 |
| 11636 | NanoString Bothell, WA Manufacturing Research Associate I BS in molecular biology, biochemistry, or related Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. This position is Non-Exempt. etc. | 4/7/2020 |
| 11637 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in biology, biochemistry, or related Exp: 0-2 years |
We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. The ideal candidate should have good organizational skills, possess good problem solving, communication and interpersonal skills and to adapt rapidly to new challenges. We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. etc. | 4/7/2020 |
| 11638 | Nanosyn Santa Clara, CA Associate Scientist / Analytical Chemist BS/MS in chemistry Exp: 1+ year(s) |
Nanosyn is currently seeking a highly motivated candidate to join the analytical and compounds management team in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of characterization, purification, QC, data processing, etc. for Nanosyn’s chemistry/biology services. She/he will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have at least 1 year of relevant experience, very strong organizational skills, the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. etc. | 4/7/2020 |
| 11639 | NantKwest San Diego, CA Research Associate - Analytical MS Exp: 1 year |
Major Job Objective and description of responsibilities/milestones/key objectives: Assist in the running of the laboratory including purchasing, set up and maintenance of equipment; maintenance of reagent inventories; preparation and management of standard operating procedures. Support the scientific operation of the laboratory by maintaining mammalian cells in cultures and generating cell banks in GXP setting. Assist in the design and execution of in vitro experiments to isolate, expand and characterize NK cells and target cell lines. Assist in the development and validation of bioassays to determine the in vitro efficacy of NK cells against various target cell lines. etc. | 4/7/2020 |
| 11640 | Nephron Pharma West Columbia, SC Microbiology Analyst I BS in biology, microbiology, or other life science Exp: 1 year |
Position Summary: Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Demonstrate high proficiency level on tests performed. Additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. NOTE: The Primary Accountabilities and Knowledge, Skills and Abilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager. Apply quality scientific techniques in the microbiological analysis of raw materials; in-process & finished product samples to include: sterility, bioburden, identification, environmental monitoring, growth promotion, microbial recovery and media fill tests following approved procedures. etc. | 4/7/2020 |
| 11641 | NeuMoDx Ann Arbor, MI Manufacturing Specialist Reagent BS/BA in chemistry or other science Exp: 1 year |
Manufacturing Specialists are required to have a strong knowledge of manufacturing methods and techniques, process development experience, work flow understanding, ability to understand formulations and follow recipes and testing protocols for any in-process Quality checks. In this position, Manufacturing Specialists, will maintain manufacturing equipment, create work instructions, train others, often be asked to contribute to or lead projects, be cross functionally trained to work in several areas as needed. etc. | 4/7/2020 |
| 11642 | Neurocrine San Diego, CA Associate Scientist, In Vivo Biology BS/BA in biology or related Exp: 1 year |
We are seeking a highly motivated and collaborative scientist to join the In Vivo Biology group. This is a hands-on role in which the successful candidate will execute behavioral experiments in both genetic and pharmacological rodent models to evaluate novel treatments for psychiatric, neurodevelopmental, and neurodegenerative disorders. Within a dynamic and engaging environment, you will interact with scientific investigators to plan and execute preclinical rodent studies. Strong technical skills and excellent communication ability are required. etc. | 4/7/2020 |
| 11643 | New England Biolabs Ipswich, MA Materials Handler HS diploma Exp: 1+ year(s) |
The Shipping Department at New England Biolabs (NEB) is inviting candidates for the position of Part-Time Shipping Clerk. The hours of this job are Monday through Friday from 3:00 pm - 8:00 pm. Primary Responsibilities: Efficiently and accurately pick and pack customer orders for shipment. Process product shipments utilizing electronic SAP/ ERP system. Support end of day procedures and ensure all customer packages are ready for delivery. Maintain and organize the shipping and warehouse area. Manage inventory and restocking of finished goods materials. Work closely with the Monarch Kit Team. etc. | 4/7/2020 |
| 11644 | Newport Laboratories Worthington, MN Technician II, Bio/Pharm Prod - Media Preparation BS/BA Exp: Not necessary for BS/BA candidates |
In this position, the incumbent will be trained in the set-up, operations, and troubleshooting of the equipment in the production areas, with focus on media preparation and equipment cleaning and sterilization. Additional duties will include documentation of work and specific computer functions. Must integrate company initiatives into work practices. Responsible for safely producing vaccines which meet all product specifications in accordance with current Good Manufacturing Practice standards. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. etc. | 4/7/2020 |
| 11645 | Nitto Milford, MA Equipment Maintenance Technician HS diploma/AS/AA Exp: 0-10+ years |
The Equipment Maintenance Technician is responsible for performing maintenance activity on process and process support equipment in accordance with departmental schedules. Key Job Responsibilities: Responsible for execution all assigned work as described by written procedures (SOPs, PM work orders, or equipment manuals). Responsible for performing all work using all prescribed safety procedures. Responsible for periodic inspections of equipment to ensure they are operating properly and safely. Assist with installation of equipment and write basic safety and maintenance procedures. Must serve on rotation for on call support and be able to respond as required. etc. | 4/7/2020 |
| 11646 | Nobel Life Sciences Woodbine, MD Animal Care Tech BS Exp: 1+ year(s) |
The Animal CareTech is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Vivarium Manager. Responsibilities include but are not limited to: Read, understand and follow all SOP’s, Quality Assurance Standards and perform duties in accordance with the study protocol. Monitor daily animal health and wellness checks and report any abnormal animal conditions to the supervisor and/or the Study Director and record observations in appropriate logs. Ensure that all animals are fed the proper diet and have adequate water within the date and time requirements. Clean and disinfect animal holding rooms daily. Assist Study Director with the performance of animal related procedures, as needed. etc. | 4/7/2020 |
| 11647 | Nobel Life Sciences Woodbine, MD Animal Lab Tech BS Exp: 1+ year(s) |
The Animal Lab Tech is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Vivarium Manager. Responsibilities include but are not limited to:Perform duties in accordance with relevant study protocols and the Standard Operating Procedures (SOPs).Follow and perform standard operating procedures (SOP) & Protocols on study and stock animals, including, but not limited to: clinical observations, food consumptions, body weights, urine collection, administering anesthesia, mating procedures, blood draws dose administration, restraint, euthanasia, catheter placement, feeding, food removal, on laboratory animals. etc. | 4/7/2020 |
| 11648 | Nobel Life Sciences Woodbine, MD QC Associate BS Exp: 1+ year(s) |
The QC Associate is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to Sr. Vice President and a Consulting Quality Assurance Unit. Responsibilities include but are not limited to: 1. Become and maintain intimate familiarity with all applicable FDA and EPA GLP and other appropriate regulations and guidelines as well as with the company SOPs and other QA systems. 2. Supervise day to day quality control operations and documentation. 3. Assist in writing and reviewing standard operating procedures, study protocols and reports. etc. | 4/7/2020 |
| 11649 | Nordson Salem, NH Production Associate I (Balloon) Third Shift HS diploma or equivalent Exp: No experience required |
Position consists of manufacturing of medical components in a clean room environment while under general supervision in accordance with specifications and written procedures. This position may include machine operation, manual production using hand tools, visual inspection, physical measurements, and packaging of finished product. This position requires the ability to work with small and delicate components using a high degree of dexterity and accuracy. This position requires direct contact with medical grade components. etc. | 4/7/2020 |
| 11650 | Nordson Chippewa Falls, WI Assembler Unspecified Exp: 1-3 year(s) |
Essential Job Duties and Responsibilities: Review bills of materials and insure parts are available in the assembly area to meet customer delivery date. Prep assembly parts according to customer order. Prep die bodies after chrome plating by stoning the bodies. Study blueprints and/or specifications to plan sequences of operations for fabricating tools, dies, or assemblies. Lift, position, and secure machined parts on worktables using hoists and/or vises. Fit and assemble parts to make dies, using machine tools and hand tools. File, grind, shim, and adjust different parts to properly fit them together. etc. | 4/7/2020 |
| 11651 | Norwich Pharma Services Norwich, NY MDAS Research Assistant BS in chemistry or related Exp: 1-2 year(s) |
The Method Development and Analytical Services (MDAS) Research Assistant is a technical resource in performing the analytical testing necessary to support development and commercialization of new pharmaceutical products. The MDAS Research Assistant is responsible for performing the bench chemistry testing for release, stability and product characterization. The MDAS Research Assistant will work under the supervision of more experienced technical staff. ORGANIZATION STRUCTURE: The Research Associate typically reports to a Group Supervisor/Leader, Manager or Director. RESPONSIBILITIES: Hands-on laboratory bench work and sample testing supporting development of pharmaceutical products. This includes but not limited to performing assay, related compounds testing, dissolution, uniformity, and other tests to characterize and demonstrate product performance. Perform laboratory bench work to develop, optimize, and troubleshoot analytical methods for testing raw materials and products (semi-finished and finished) under the guidance of senior staff. etc. | 4/7/2020 |
| 11652 | Notal Vision Manassas, VA Field Service Engineer BS in electronics, engineering, or related Exp: 1-3 year(s) |
The Field Service Engineer, under supervision and direction of the Director, Operations & Business Performance, installs, calibrates, tests, repairs, upgrades and performs preventative maintenance on specified Notal Vision imaging devices at customer sites and the company’s Headquarters. Deep acumen in of ophthalmic imaging devices is required to understand, assess and act on the needs of the customers and to mitigate loss of testing. ROLES AND RESPONSIBILITIES: Responsibilities of the Field Service Engineer include but are not limited to the following: Provide technical support for imaging devices in multiple care and support settings. etc. | 4/7/2020 |
| 11653 | B. Braun Fremont, CA IV Tech I National Pharmacy Tech certification Exp: 1 year in related |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. | 4/5/2020 |
| 11654 | AGC Biolgics Seattle, WA QC Associate I BS/BA Exp: 1-3 years relevant experience |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. Supports projects / initiatives / team goals by delivering on all assigned tasks. Analyzes issues and makes decisions based on standardized processes and procedures under direct supervision | 4/5/2020 |
| 11655 | AGC Biolgics Bothell, WA Process Transfer Technical Writer BS in sciences/engineering Exp: 0 years |
The Process Transfer Technical Writer is a role for individuals with a STEM background that provides the opportunity to learn and support biotechnology manufacturing operations. Working under the direction of departmental staff, individuals in this role take part in generating key manufacturing documentation, resolving technical issues, and providing training to manufacturing operators. Generating process instructions and batch records from pre-established templates, using source data and information provided, and as instructed and guided by Process Transfer Staff | 4/5/2020 |
| 11656 | AGC Biolgics Bothell, WA Manufacturing Associate I-IV, Downstream BS in chemistry/biology Exp: 1-8 years in aseptic processing |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment | 4/5/2020 |
| 11657 | AGC Biolgics Bothell, WA Manufacturing Associate, Downstream BS in chemistry/biology Exp: 1-8 years in aseptic processing |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment | 4/5/2020 |
| 11658 | AGC Biolgics Bothell, WA Associate Business Development Partner BS or MS in biological sciences Exp: 1-3 years in pharma, cdmo, or biotech |
As Associate Business Development Partner, you will transform customer Request for Proposals (RFP) into winning proposals and be very involved during the sales process by providing technical/operational expertise. The individual selected will interact intensively with both business development and technical colleagues and senior management and will work in a dynamic and fast-paced environment. | 4/5/2020 |
| 11659 | AGC Biolgics Bothell, WA Accounting Specialist I/II AA in accounting preferred, HS Diploma/GED Exp: 0-2 years in accounting |
Input vendor invoices into the system in a timely and accurate manner (including 2 way/3 way match). Assist in the preparation of the weekly check runs. Oversee the maintenance of our expense reporting tool (Acubiz) including user maintenance, recording expenses in the GL, and expense report approvals. Ensure all invoices/payments are properly filed | 4/5/2020 |
| 11660 | AGTC Gainesville, FL QA Specialist I/II/III BS in sciences Exp: 0 years in QA |
The Quality Assurance (QA) Specialist provides quality oversight of internal and external activities, documentation and processes to assure compliance with company procedures and FDA regulations and assists with tasks necessary to achieve departmental and company goals. Support the development, implementation, and improvement of corporate quality systems that support early, mid and late phase gene therapy clinical programs. Increase compliance awareness and promote a culture of quality throughout the company, with a focus on laboratory and manufacturing operations | 4/5/2020 |
| 11661 | AGTC Gainesville, FL Process Development Associate, Downstream BS in biological sciences/engineering Exp: 1 year in biologics |
The PD Associate is responsible for performing downstream process development activities as needed, working independently, with minimal supervision, and on a timely basis, in order to achieve department and/or company goals. Conduct downstream unit operations, including hands-on work with column chromatography and filtration techniques, for the optimization of downstream process unit operations. Collect, analyze, record, and summarize data in the course of biologics production and processing. | 4/5/2020 |
| 11662 | Ajinomoto Bio-Pharma San Diego, CA Facilities Assistant HS Diploma/GED Exp: 0-2 years |
The facilities assistant is responsible for general maintenance of facility areas including office, conference room, and utility areas. The position provides general support including cleaning, painting, uncrating and assembly, and ordering and stocking of facility supplies, spare parts, and equipment. Maintain facility in a presentation-ready, clean state. Assist with maintenance activities as overseen by a senior member. | 4/5/2020 |
| 11663 | Ajinomoto Bio-Pharma San Diego, CA Drug Product Manufacturing Assistant – 1st and 2nd Shift Opportunities HS Diploma/GED Exp: 0-2 years in lab or manufacturing |
The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Implements production and manufacturing procedures. Performs visual inspection. | 4/5/2020 |
| 11664 | Ajinomoto Bio-Pharma San Diego, CA Aseptic Cleaning Technician HS Diploma/GED Exp: 0-2 years in aspectic/GMP cleanroom |
The Aseptic Cleaning Assistant performs tasks of the production operation specific to aseptic cleaning and sterilization of processing equipment, parts and rooms. The Assistant maintains batch record documentation and logs as required by corporation and regulatory agencies. This role prepares, according to procedures, various stock solutions and buffers as required by the production process. In addition, this position is responsible for operating general production equipment (such as autoclaves). | 4/5/2020 |
| 11665 | Aklesogen Peachtree Corners, GA Research Associate BS/BA in clinical, health or life sciences Exp: 1 year in lab |
This individual is a Research Associate who will work with a team of research associates and scientist at AKESOgen. The Research Associate will work under the general direction of a Team Lead. This individual will perform extractions on a variety of sample types, genotyping on Affymetrix and/or Illumina platform equipment maintenance, solution and reagent preparation in addition to other tasks in laboratory. Operate automated liquid handling platforms for sample processing, DNA/RNA extraction and quantification instruments. | 4/5/2020 |
| 11666 | Akorn Somerset, NJ Sanitization Associates HS Diploma/GED Exp: 1 year in pharma/aspectic manufacturing |
All Sanitization Associates are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. Compliance with associated SOPs and training requirements. Removal of used scrubs and coveralls into appropriate bins. Stocking of consumable items, such as bouffant hats and beard covers | 4/5/2020 |
| 11667 | Alamo Pharma Services Baltimore, MD Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in b2b sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 4/5/2020 |
| 11668 | Alamo Pharma Services Los Angeles, CA Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in b2b sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 4/5/2020 |
| 11669 | Alamo Pharma Services Austin, TX Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in b2b sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 4/5/2020 |
| 11670 | Alcami Wilmington, NC Process Engineer I BS in engineering/pharmacy/chemistry Exp: 0-2 years |
The Process Engineer I/II is accountable for driving results in a fast-paced environment by providing technical support for the of tablets and capsules for commercial distribution and clinical use. The Process Engineer I/II in this position will provide technical assistance including but not limited to the following: transfer of new process and technologies into the company and writing appropriate documentation to support process transfer and validation activities, sourcing and qualification of equipment and components, troubleshooting current validated processes, initiate process deviations and conduct investigations. | 4/5/2020 |
| 11671 | Alcami Charleston, SC Process Engineer BS in engineering/pharmacy/chemistry Exp: 0-2 years in technical support of sterile manufacturing |
The Process Engineer I (Sterile) for our parenteral site in Charleston, SC is accountable for driving results in a fast-paced environment by providing technical support for the manufacturing facility, including, troubleshooting validated processes, process deviations and investigations, transfers of new processes and technologies into the site and preparation of documentation to support validation and process transfer activities. | 4/5/2020 |
| 11672 | Alcami Wilmington, NC Metrology Calibration Technician I AS or AAS Exp: 1-3 years in calibration/instrumentation |
The Metrology Calibration Technician I is accountable for driving results in a fast-paced environment by performing scheduled and unscheduled calibration, preventive maintenance (PM), and repair tasks in support of typical analytical and/or process instrumentation prevalent within the bio-pharmaceutical industry. Examples of instrumentation supported include but are not limited to: temperature and pressure measuring instruments, micrometers, calipers, torque testers, hardness testers, balances | 4/5/2020 |
| 11673 | B. Braun Fremont, CA IV Tech I National Pharmacy Tech certification Exp: 1 year in related |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. | 4/5/2020 |
| 11674 | AGC Biolgics Seattle, WA QC Associate I BS/BA Exp: 1-3 years relevant experience |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. Supports projects / initiatives / team goals by delivering on all assigned tasks. Analyzes issues and makes decisions based on standardized processes and procedures under direct supervision | 4/5/2020 |
| 11675 | AGC Biolgics Bothell, WA Process Transfer Technical Writer BS in sciences/engineering Exp: 0 years |
The Process Transfer Technical Writer is a role for individuals with a STEM background that provides the opportunity to learn and support biotechnology manufacturing operations. Working under the direction of departmental staff, individuals in this role take part in generating key manufacturing documentation, resolving technical issues, and providing training to manufacturing operators. Generating process instructions and batch records from pre-established templates, using source data and information provided, and as instructed and guided by Process Transfer Staff | 4/5/2020 |
| 11676 | AGC Biolgics Bothell, WA Manufacturing Associate I-IV, Downstream BS in chemistry/biology Exp: 1-8 years in aseptic processing |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment | 4/5/2020 |
| 11677 | AGC Biolgics Bothell, WA Manufacturing Associate, Downstream BS in chemistry/biology Exp: 1-8 years in aseptic processing |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment | 4/5/2020 |
| 11678 | AGC Biolgics Bothell, WA Associate Business Development Partner BS or MS in biological sciences Exp: 1-3 years in pharma, cdmo, or biotech |
As Associate Business Development Partner, you will transform customer Request for Proposals (RFP) into winning proposals and be very involved during the sales process by providing technical/operational expertise. The individual selected will interact intensively with both business development and technical colleagues and senior management and will work in a dynamic and fast-paced environment. | 4/5/2020 |
| 11679 | AGC Biolgics Bothell, WA Accounting Specialist I/II AA in accounting preferred, HS Diploma/GED Exp: 0-2 years in accounting |
Input vendor invoices into the system in a timely and accurate manner (including 2 way/3 way match). Assist in the preparation of the weekly check runs. Oversee the maintenance of our expense reporting tool (Acubiz) including user maintenance, recording expenses in the GL, and expense report approvals. Ensure all invoices/payments are properly filed | 4/5/2020 |
| 11680 | AGTC Gainesville, FL QA Specialist I/II/III BS in sciences Exp: 0 years in QA |
The Quality Assurance (QA) Specialist provides quality oversight of internal and external activities, documentation and processes to assure compliance with company procedures and FDA regulations and assists with tasks necessary to achieve departmental and company goals. Support the development, implementation, and improvement of corporate quality systems that support early, mid and late phase gene therapy clinical programs. Increase compliance awareness and promote a culture of quality throughout the company, with a focus on laboratory and manufacturing operations | 4/5/2020 |
| 11681 | AGTC Gainesville, FL Process Development Associate, Downstream BS in biological sciences/engineering Exp: 1 year in biologics |
The PD Associate is responsible for performing downstream process development activities as needed, working independently, with minimal supervision, and on a timely basis, in order to achieve department and/or company goals. Conduct downstream unit operations, including hands-on work with column chromatography and filtration techniques, for the optimization of downstream process unit operations. Collect, analyze, record, and summarize data in the course of biologics production and processing. | 4/5/2020 |
| 11682 | Ajinomoto Bio-Pharma San Diego, CA Facilities Assistant HS Diploma/GED Exp: 0-2 years |
The facilities assistant is responsible for general maintenance of facility areas including office, conference room, and utility areas. The position provides general support including cleaning, painting, uncrating and assembly, and ordering and stocking of facility supplies, spare parts, and equipment. Maintain facility in a presentation-ready, clean state. Assist with maintenance activities as overseen by a senior member. | 4/5/2020 |
| 11683 | Ajinomoto Bio-Pharma San Diego, CA Drug Product Manufacturing Assistant – 1st and 2nd Shift Opportunities HS Diploma/GED Exp: 0-2 years in lab or manufacturing |
The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Implements production and manufacturing procedures. Performs visual inspection. | 4/5/2020 |
| 11684 | Ajinomoto Bio-Pharma San Diego, CA Aseptic Cleaning Technician HS Diploma/GED Exp: 0-2 years in aspectic/GMP cleanroom |
The Aseptic Cleaning Assistant performs tasks of the production operation specific to aseptic cleaning and sterilization of processing equipment, parts and rooms. The Assistant maintains batch record documentation and logs as required by corporation and regulatory agencies. This role prepares, according to procedures, various stock solutions and buffers as required by the production process. In addition, this position is responsible for operating general production equipment (such as autoclaves). | 4/5/2020 |
| 11685 | Aklesogen Peachtree Corners, GA Research Associate BS/BA in clinical, health or life sciences Exp: 1 year in lab |
This individual is a Research Associate who will work with a team of research associates and scientist at AKESOgen. The Research Associate will work under the general direction of a Team Lead. This individual will perform extractions on a variety of sample types, genotyping on Affymetrix and/or Illumina platform equipment maintenance, solution and reagent preparation in addition to other tasks in laboratory. Operate automated liquid handling platforms for sample processing, DNA/RNA extraction and quantification instruments. | 4/5/2020 |
| 11686 | Akorn Somerset, NJ Sanitization Associates HS Diploma/GED Exp: 1 year in pharma/aspectic manufacturing |
All Sanitization Associates are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. Compliance with associated SOPs and training requirements. Removal of used scrubs and coveralls into appropriate bins. Stocking of consumable items, such as bouffant hats and beard covers | 4/5/2020 |
| 11687 | Alamo Pharma Services Baltimore, MD Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in b2b sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 4/5/2020 |
| 11688 | Alamo Pharma Services Los Angeles, CA Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in b2b sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 4/5/2020 |
| 11689 | Alamo Pharma Services Austin, TX Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in b2b sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 4/5/2020 |
| 11690 | Alcami Wilmington, NC Process Engineer I BS in engineering/pharmacy/chemistry Exp: 0-2 years |
The Process Engineer I/II is accountable for driving results in a fast-paced environment by providing technical support for the of tablets and capsules for commercial distribution and clinical use. The Process Engineer I/II in this position will provide technical assistance including but not limited to the following: transfer of new process and technologies into the company and writing appropriate documentation to support process transfer and validation activities, sourcing and qualification of equipment and components, troubleshooting current validated processes, initiate process deviations and conduct investigations. | 4/5/2020 |
| 11691 | Alcami Charleston, SC Process Engineer BS in engineering/pharmacy/chemistry Exp: 0-2 years in technical support of sterile manufacturing |
The Process Engineer I (Sterile) for our parenteral site in Charleston, SC is accountable for driving results in a fast-paced environment by providing technical support for the manufacturing facility, including, troubleshooting validated processes, process deviations and investigations, transfers of new processes and technologies into the site and preparation of documentation to support validation and process transfer activities. | 4/5/2020 |
| 11692 | Alcami Wilmington, NC Metrology Calibration Technician I AS or AAS Exp: 1-3 years in calibration/instrumentation |
The Metrology Calibration Technician I is accountable for driving results in a fast-paced environment by performing scheduled and unscheduled calibration, preventive maintenance (PM), and repair tasks in support of typical analytical and/or process instrumentation prevalent within the bio-pharmaceutical industry. Examples of instrumentation supported include but are not limited to: temperature and pressure measuring instruments, micrometers, calipers, torque testers, hardness testers, balances | 4/5/2020 |
| 11693 | B. Braun Irvine, CA QC Microbiology Assoc I Associates or HS Diploma/GED Exp: 0-2 years related |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. Responsible for microbiological sample receiving/labeling/preparation/sampling/test/ counting/checking and recording of data analysis on finished products, stability test samples and any other test requisitions as directed. Supports the department in ensuring laboratory equipment performance, i.e. scheduling and execution of equipment qualification (IQ/OQ/PQ), calibration, maintenance and trouble shooting. | 4/5/2020 |
| 11694 | B. Braun Irvine, CA QC Microbiology Assoc I Associates or HS Diploma/GED Exp: 0-2 years related |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. Responsible for microbiological sample receiving/labeling/preparation/sampling/test/ counting/checking and recording of data analysis on finished products, stability test samples and any other test requisitions as directed. Supports the department in ensuring laboratory equipment performance, i.e. scheduling and execution of equipment qualification (IQ/OQ/PQ), calibration, maintenance and trouble shooting. | 4/5/2020 |
| 11695 | B. Braun Irvine, CA QC Microbiology Assoc I Associates or HS Diploma/GED Exp: 0-2 years related |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. Responsible for microbiological sample receiving/labeling/preparation/sampling/test/ counting/checking and recording of data analysis on finished products, stability test samples and any other test requisitions as directed. Supports the department in ensuring laboratory equipment performance, i.e. scheduling and execution of equipment qualification (IQ/OQ/PQ), calibration, maintenance and trouble shooting. | 4/5/2020 |
| 11696 | B. Braun Irvine, CA QC Microbiology Assoc I Associates or HS Diploma/GED Exp: 0-2 years related |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. Responsible for microbiological sample receiving/labeling/preparation/sampling/test/ counting/checking and recording of data analysis on finished products, stability test samples and any other test requisitions as directed. Supports the department in ensuring laboratory equipment performance, i.e. scheduling and execution of equipment qualification (IQ/OQ/PQ), calibration, maintenance and trouble shooting. | 4/5/2020 |
| 11697 | B. Braun San Diego, CA IV Tech I National Pharmacy Tech certification Exp: 1 year in related |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. | 4/5/2020 |
| 11698 | B. Braun San Diego, CA IV Tech I National Pharmacy Tech certification Exp: 1 year in related |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. | 4/5/2020 |
| 11699 | B. Braun Irvine, CA Mixing Tech I (Mixing) HS Diploma/GED Exp: 1-2 years in related |
Perform daily, weekly and monthly clean-up of equipment, plumbing and facilities in the Mixing complex to censure that they are cleaned and properly sanitized to meet government and industry standards. Assist Mixing Technician II with elementary mixing tasks. Performs technical and manual duties required to mix chemical and physical formulation of products. Includes all steps of production from receiving raw materials to providing solutions for production lines. | 4/5/2020 |
| 11700 | B. Braun Irvine, CA Mixing Tech I (Mixing) HS Diploma/GED Exp: 1-2 years in related |
Perform daily, weekly and monthly clean-up of equipment, plumbing and facilities in the Mixing complex to censure that they are cleaned and properly sanitized to meet government and industry standards. Assist Mixing Technician II with elementary mixing tasks. Performs technical and manual duties required to mix chemical and physical formulation of products. Includes all steps of production from receiving raw materials to providing solutions for production lines. | 4/5/2020 |
| 11701 | B. Braun Beltsville, MD IV Tech I National Pharmacy Tech certification Exp: 1 year in related |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. | 4/5/2020 |
| 11702 | B. Braun Beltsville, MD IV Tech I National Pharmacy Tech certification Exp: 1 year in related |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. | 4/5/2020 |
| 11703 | LaunchCOde Plano, TX Entry Level Mainframe Systems Engineer HS Diploma/GED Exp: Entry Level |
Selected candidates will be required to attend both virtual, at-home training and a series of in-person training beginning in Pittsburgh, PA. After training is completed, you will continue your learning journey as a Mainframe Systems Engineer in one of the hiring company’s locations across 20+ cities. | 4/5/2020 |
| 11704 | LaunchCOde Plano, TX Entry Level Mainframe Systems Engineer HS Diploma/GED Exp: Entry Level |
Selected candidates will be required to attend both virtual, at-home training and a series of in-person training beginning in Pittsburgh, PA. After training is completed, you will continue your learning journey as a Mainframe Systems Engineer in one of the hiring company’s locations across 20+ cities. | 4/5/2020 |
| 11705 | Acutus Medical Carlsbad, CA UX Designer/Researcher BS in sciences/engineering Exp: 1 year related work |
The User Interface Designer/Researcher conducts iterative design activities to help build best-in-class customer experiences across all Acutus hardware and software platforms and touchpoints. The UX Designer/Researcher is responsible for driving the user experience across a wide array of projects. This role collaborates with customers, product managers, software/system design leads, and various engineering leads to ensure the design deliverables successfully and efficiently move each feature from concept to final product. | 4/4/2020 |
| 11706 | Acutus Medical Carlsbad, CA IT Specialist BS/BA in related Exp: 6 months in computer support |
Responsible for providing technical assistance and support related to computer systems, printers, AV equipment, hardware or software. Responds to queries, runs diagnostic programs, isolates problem and determines and implement solutions. Maintain and support IT system security in the organization to ensure safety of data and IT systems. Deploy and maintain computer work stations and printers | 4/4/2020 |
| 11707 | Adaptimmune Philadelphia, PA Manufacturing Cell Therapy Specialist BS/BA in biological sciences/engineering Exp: 1 year in lab |
Performs cell manufacturing related activities while wearing clean room attire in an aseptic cGMP manner. Documents production operations in corresponding batch records and log books per established procedures ensuring accuracy and timely completion. Identifies real time manufacturing issues (deviations and atypical results) and communicates them to the Manufacturing Manager and the Quality team in a timely manner. Inputting and uploading of manufacturing data in real time to existing database. | 4/4/2020 |
| 11708 | Adaptive Biotechnologies Seattle, WA Research Assistant, Research & Development BS/BA in biological sciences/engineering Exp: 1-2 years in research lab |
The Research Assistant will perform regular upkeep and maintenance of lab equipment and reagents for the R&D labs at Adaptive. They will work with people across multiple departments, including the environmental health and safety officer, facilities & equipment specialist, and material handling team, in addition to closely working with the multiple teams within MRI and Molecular Product Development, to create a safe and well-prepared lab environment. Successful candidates will be able to proactively assess and address the needs of the team, while being a positive and approachable source of information regarding safe lab practices, and acquisition of materials for experiments. | 4/4/2020 |
| 11709 | Adaptive Biotechnologies Seattle, WA Research Assistant, Research & Development BS/BA in biological sciences/engineering Exp: 1-2 years in research lab |
The Research Assistant will perform regular upkeep and maintenance of lab equipment and reagents for the R&D labs at Adaptive. They will work with people across multiple departments, including the environmental health and safety officer, facilities & equipment specialist, and material handling team, in addition to closely working with the multiple teams within MRI and Molecular Product Development, to create a safe and well-prepared lab environment. | 4/4/2020 |
| 11710 | Adaptive Biotechnologies Seattle, WA Research Assistant, Molecular Product Development BS/BA in genetics, immunology, bioengineering or related Exp: 1-3 years in diagnostic/med devices |
This successful candidate will be responsible for performing various tasks to support the laboratory technical staff including equipment maintenance and calibration, monitoring and stocking of supplies and reagents, and overall cleanliness of the laboratory work-spaces within the Molecular Product Development (MPD) laboratory. Perform routine instrument calibration, assist facilities with IQ/OQ of instruments (PQ as needed), and track and schedule instrument maintenance. | 4/4/2020 |
| 11711 | Adaptive Biotechnologies Seattle, WA Biological Sample Management Specialist II Associates or BS/BA Exp: 1 year in clinical lab |
The BSM Specialist II position will join the Biological Sample Management (BSM) group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support sample management and chain of custody for Adaptive’s immunosequencing services that includes research, clinical projects, and diagnostic testing. Primary responsibility is to receive and accession samples into the Laboratory Information System (LIMS) used by BSM AND/OR perform sample discards and returns per standard retention times, or by request. | 4/4/2020 |
| 11712 | Adaptive Biotechnologies Seattle, WA Lab Associate I, Antigen Map BS/BA in biological sciences Exp: 1-2 years in research lab |
As a member of the Antigen Map Production Lab, you will contribute to the generation of the samples required to generate this TCR-Antigen. Monitor inventory levels and formulate reagents as needed. Stock and stage materials to support operations. Handle biohazardous and chemical waste. Support cell isolation, expansion and stimulation as requested | 4/4/2020 |
| 11713 | Adaptive Biotechnologies Seattle, WA Research Associate I BS/BA in biological sciences Exp: 1-3 years lab experience |
Adaptive is seeking a research associate I with an aptitude for learning to join our dynamic and collaborative R&D team. You will partner with other researchers and computational biologists in the development of new and optimization of existing assays for transition into a service lab and/or kit. Work in tandem with team to develop PCR-based assays for immune system profiling by next generation sequencing. DNA/RNA extraction from large number of samples. | 4/4/2020 |
| 11714 | Adare Pharmaceuticals Vandalia, OH Quality Assurance Technician (Night Shift) BS in chemical/biological sciences Exp: 0-2 years in pharma |
This position is responsible for providing quality support to the manufacturing floor, auditing batch production documentation, dispositioning intermediates and equipment after cleaning, performing in process checks, reviewing and approving incident reports, revise quality documents (e.g. SOP, protocols, methods), and ensuring adherence to cGMP. | 4/4/2020 |
| 11715 | Adare Pharmaceuticals Vandalia, OH Operator I HS Diploma/GED Exp: 1 year in manufacturing |
This is an entry level position at Adare Pharmaceuticals, Inc. (Adare) and the skills learned during training will enable the new operator to perform essential job functions. The essential job function are to produce specified products by the mixing, blending, and combining of raw materials as specified by written procedures. This position is night shift working 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday. | 4/4/2020 |
| 11716 | Adare Pharmaceuticals Vandalia, OH Regulatory Affairs Specialist ll BS/BA Exp: 1 year in regulatory affiars |
Provide diverse regulatory support to the Regulatory Affairs Department as outlined in essential duties and responsibilities below. Assesses change control documentation and technical documents for incorporation of the information into regulatory submissions. Prepares regulatory submissions for annual reports and assists as necessary with preparation of new regulatory submissions and amendments. Demonstrates an understanding of health authority reporting obligations throughout annual report preparation and seeks guidance when needed to address complex changes. | 4/4/2020 |
| 11717 | Adarza Biosystems Maryland Heights, MO Research Associate – Research and Development BS to relevant sciences Exp: 0-2 years lab experience |
Responsibilities will broadly include supporting the development of new biomarker assays with Adarza’s proprietary AIR™ technology on the ZIVA platform. You will work as part of a team utilizing your laboratory skills to develop and validate immunoassays, as well as provide routine analysis of biological samples for early access clients. The successful candidate will be responsible for reagent preparation, specimen processing, developing and running AIR™ assays. Candidates will be asked to communicate previous work experience successes during the interview process to demonstrate their abilities and the relevance of their experience | 4/4/2020 |
| 11718 | Adma Biolgics Boco Raton, FL Technician I, Manufacturing Purification BS/BA in chemistry/life sciences Exp: 0-2 years |
This position is under direct supervision of the Group Leader. It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. | 4/4/2020 |
| 11719 | Adma Biolgics Boco Raton, FL Document Assistant - Temporary College enrolled or recent graduate Exp: 1-2 years in document management |
The Document Assistant will Create, format, revise and proof read controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control. Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies. | 4/4/2020 |
| 11720 | Adma Biolgics Boco Raton, FL QC Lab Support Associate l BS in biological/chemical/medical sciences Exp: 1-3 years in regulated lab |
The QC Lab Support Associate I will Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. | 4/4/2020 |
| 11721 | Adma Biolgics Boco Raton, FL Chemist I BS in biological/chemical sciences Exp: 0-3 years in lab setting |
The Chemist I will Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. Perform quality control chemistry and/or Immunoassays for raw materials, in-process and final products according to approved Standard Operating Procedures (SOP’s). Perform instument calibration or qualification according to written procedures. | 4/4/2020 |
| 11722 | Admera Health South Plainfield, NJ Associate Scientist I-PM (Non-Lab Position) BS or MS in biological sciences Exp: 1+ years in lab |
Relay standard information on next generation sequencing applications to customers. Standard communication with prospective, current, and past customers. Co-coordinating multiple genomic projects with excellent documentation skills and communication to customers. Materials purchasing support for laboratory team | 4/4/2020 |
| 11723 | Admera Health South Plainfield, NJ Regional Sales Manager-East Coast BS/BA in biological/life sciences Exp: 1 year with genomics/gemonics related |
Achieve annual sales goals within defined territory/accounts through development, maintenance, and enhancement of customer accounts development, maintenance, and enhancement of customer accounts. Responsibility for managing all business accounts in assigned region/territory including implementing strategies in developing new growth of accounts. Drive the marketing process for the territory by creating a marketing plan, registering/planning/ attending local vendor shows, creating and working with Marketing and PM team to execute email campaigns | 4/4/2020 |
| 11724 | Biotechne Minneapolis, MN Laboratory Production Assistant HS Diploma/GED Exp: 0-2 years |
You will be responsible for assisting in the Clinical Controls Product Finishing Department with the bottling operation and the other activities involved in the product finishing process. Label product, operate the labeling equipment. Upon release of product by QA lab, count, verify and record number of finished products. Assist with monthly cleaning of clean room, including counters, laminer hoods, torque, labeler, sinks, and all work areas. | 4/4/2020 |
| 11725 | Biotechne Minneapolis, MN Administrative Support / Shipping Assistant HS Diploma/GED Exp: 0-2 years |
The responsibilities of this position are to support the DD OEM Accounts / Shipping Manager and Shipping Department’s activities by performing order processing, proofing, set assembly, shipping and other related duties. Order processing in our ERP System. Assist in preparing final shipping documents for OEM, International, Survey and Domestic shipments. Assist with maintaining Distributor, OEM and Survey customer orders and shipping records | 4/4/2020 |
| 11726 | Biotechne Minneapolis, MN Lab Assistant HS Diploma/GED Exp: 0-2 years |
The responsibilities of this position include processing raw biological materials for the use in manufacturing our products, maintaining and cleaning production equipment and containers, and completing required paperwork. Perform other duties as needed. Processes raw biological materials for the use in manufacturing our products. Maintains production equipment and containers | 4/4/2020 |
| 11727 | Biotechne Minneapolis, MN Research Associate, Cell Culture and Stem Cell Media Operations BS/BA in biological sciences Exp: 0-2 years in lab |
The main responsibility of this position it to maintain production of mouse embryonic fibroblasts. Additional responsibilities include media and supplement production, QC testing of methylcellulose-containing cell culture media, and cell culture of multiple cell lines. Perform additional duties as assigned. Preferred skills include cell culture, high attention to detail, strong communication and organizational skills. | 4/4/2020 |
| 11728 | Acutus Medical Carlsbad, CA UX Designer/Researcher BS in sciences/engineering Exp: 1 year related work |
The User Interface Designer/Researcher conducts iterative design activities to help build best-in-class customer experiences across all Acutus hardware and software platforms and touchpoints. The UX Designer/Researcher is responsible for driving the user experience across a wide array of projects. This role collaborates with customers, product managers, software/system design leads, and various engineering leads to ensure the design deliverables successfully and efficiently move each feature from concept to final product. | 4/4/2020 |
| 11729 | Acutus Medical Carlsbad, CA IT Specialist BS/BA in related Exp: 6 months in computer support |
Responsible for providing technical assistance and support related to computer systems, printers, AV equipment, hardware or software. Responds to queries, runs diagnostic programs, isolates problem and determines and implement solutions. Maintain and support IT system security in the organization to ensure safety of data and IT systems. Deploy and maintain computer work stations and printers | 4/4/2020 |
| 11730 | Adaptimmune Philadelphia, PA Manufacturing Cell Therapy Specialist BS/BA in biological sciences/engineering Exp: 1 year in lab |
Performs cell manufacturing related activities while wearing clean room attire in an aseptic cGMP manner. Documents production operations in corresponding batch records and log books per established procedures ensuring accuracy and timely completion. Identifies real time manufacturing issues (deviations and atypical results) and communicates them to the Manufacturing Manager and the Quality team in a timely manner. Inputting and uploading of manufacturing data in real time to existing database. | 4/4/2020 |
| 11731 | Adaptive Biotechnologies Seattle, WA Research Assistant, Research & Development BS/BA in biological sciences/engineering Exp: 1-2 years in research lab |
The Research Assistant will perform regular upkeep and maintenance of lab equipment and reagents for the R&D labs at Adaptive. They will work with people across multiple departments, including the environmental health and safety officer, facilities & equipment specialist, and material handling team, in addition to closely working with the multiple teams within MRI and Molecular Product Development, to create a safe and well-prepared lab environment. Successful candidates will be able to proactively assess and address the needs of the team, while being a positive and approachable source of information regarding safe lab practices, and acquisition of materials for experiments. | 4/4/2020 |
| 11732 | Adaptive Biotechnologies Seattle, WA Research Assistant, Research & Development BS/BA in biological sciences/engineering Exp: 1-2 years in research lab |
The Research Assistant will perform regular upkeep and maintenance of lab equipment and reagents for the R&D labs at Adaptive. They will work with people across multiple departments, including the environmental health and safety officer, facilities & equipment specialist, and material handling team, in addition to closely working with the multiple teams within MRI and Molecular Product Development, to create a safe and well-prepared lab environment. | 4/4/2020 |
| 11733 | Adaptive Biotechnologies Seattle, WA Research Assistant, Molecular Product Development BS/BA in genetics, immunology, bioengineering or related Exp: 1-3 years in diagnostic/med devices |
This successful candidate will be responsible for performing various tasks to support the laboratory technical staff including equipment maintenance and calibration, monitoring and stocking of supplies and reagents, and overall cleanliness of the laboratory work-spaces within the Molecular Product Development (MPD) laboratory. Perform routine instrument calibration, assist facilities with IQ/OQ of instruments (PQ as needed), and track and schedule instrument maintenance. | 4/4/2020 |
| 11734 | Adaptive Biotechnologies Seattle, WA Biological Sample Management Specialist II Associates or BS/BA Exp: 1 year in clinical lab |
The BSM Specialist II position will join the Biological Sample Management (BSM) group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support sample management and chain of custody for Adaptive’s immunosequencing services that includes research, clinical projects, and diagnostic testing. Primary responsibility is to receive and accession samples into the Laboratory Information System (LIMS) used by BSM AND/OR perform sample discards and returns per standard retention times, or by request. | 4/4/2020 |
| 11735 | Adaptive Biotechnologies Seattle, WA Lab Associate I, Antigen Map BS/BA in biological sciences Exp: 1-2 years in research lab |
As a member of the Antigen Map Production Lab, you will contribute to the generation of the samples required to generate this TCR-Antigen. Monitor inventory levels and formulate reagents as needed. Stock and stage materials to support operations. Handle biohazardous and chemical waste. Support cell isolation, expansion and stimulation as requested | 4/4/2020 |
| 11736 | Adaptive Biotechnologies Seattle, WA Research Associate I BS/BA in biological sciences Exp: 1-3 years lab experience |
Adaptive is seeking a research associate I with an aptitude for learning to join our dynamic and collaborative R&D team. You will partner with other researchers and computational biologists in the development of new and optimization of existing assays for transition into a service lab and/or kit. Work in tandem with team to develop PCR-based assays for immune system profiling by next generation sequencing. DNA/RNA extraction from large number of samples. | 4/4/2020 |
| 11737 | Adare Pharmaceuticals Vandalia, OH Quality Assurance Technician (Night Shift) BS in chemical/biological sciences Exp: 0-2 years in pharma |
This position is responsible for providing quality support to the manufacturing floor, auditing batch production documentation, dispositioning intermediates and equipment after cleaning, performing in process checks, reviewing and approving incident reports, revise quality documents (e.g. SOP, protocols, methods), and ensuring adherence to cGMP. | 4/4/2020 |
| 11738 | Adare Pharmaceuticals Vandalia, OH Operator I HS Diploma/GED Exp: 1 year in manufacturing |
This is an entry level position at Adare Pharmaceuticals, Inc. (Adare) and the skills learned during training will enable the new operator to perform essential job functions. The essential job function are to produce specified products by the mixing, blending, and combining of raw materials as specified by written procedures. This position is night shift working 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday. | 4/4/2020 |
| 11739 | Adare Pharmaceuticals Vandalia, OH Regulatory Affairs Specialist ll BS/BA Exp: 1 year in regulatory affiars |
Provide diverse regulatory support to the Regulatory Affairs Department as outlined in essential duties and responsibilities below. Assesses change control documentation and technical documents for incorporation of the information into regulatory submissions. Prepares regulatory submissions for annual reports and assists as necessary with preparation of new regulatory submissions and amendments. Demonstrates an understanding of health authority reporting obligations throughout annual report preparation and seeks guidance when needed to address complex changes. | 4/4/2020 |
| 11740 | Adarza Biosystems Maryland Heights, MO Research Associate – Research and Development BS to relevant sciences Exp: 0-2 years lab experience |
Responsibilities will broadly include supporting the development of new biomarker assays with Adarza’s proprietary AIR™ technology on the ZIVA platform. You will work as part of a team utilizing your laboratory skills to develop and validate immunoassays, as well as provide routine analysis of biological samples for early access clients. The successful candidate will be responsible for reagent preparation, specimen processing, developing and running AIR™ assays. Candidates will be asked to communicate previous work experience successes during the interview process to demonstrate their abilities and the relevance of their experience | 4/4/2020 |
| 11741 | Adma Biolgics Boco Raton, FL Technician I, Manufacturing Purification BS/BA in chemistry/life sciences Exp: 0-2 years |
This position is under direct supervision of the Group Leader. It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. | 4/4/2020 |
| 11742 | Adma Biolgics Boco Raton, FL Document Assistant - Temporary College enrolled or recent graduate Exp: 1-2 years in document management |
The Document Assistant will Create, format, revise and proof read controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control. Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies. | 4/4/2020 |
| 11743 | Adma Biolgics Boco Raton, FL QC Lab Support Associate l BS in biological/chemical/medical sciences Exp: 1-3 years in regulated lab |
The QC Lab Support Associate I will Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. | 4/4/2020 |
| 11744 | Adma Biolgics Boco Raton, FL Chemist I BS in biological/chemical sciences Exp: 0-3 years in lab setting |
The Chemist I will Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. Perform quality control chemistry and/or Immunoassays for raw materials, in-process and final products according to approved Standard Operating Procedures (SOP’s). Perform instument calibration or qualification according to written procedures. | 4/4/2020 |
| 11745 | Admera Health South Plainfield, NJ Associate Scientist I-PM (Non-Lab Position) BS or MS in biological sciences Exp: 1+ years in lab |
Relay standard information on next generation sequencing applications to customers. Standard communication with prospective, current, and past customers. Co-coordinating multiple genomic projects with excellent documentation skills and communication to customers. Materials purchasing support for laboratory team | 4/4/2020 |
| 11746 | Admera Health South Plainfield, NJ Regional Sales Manager-East Coast BS/BA in biological/life sciences Exp: 1 year with genomics/gemonics related |
Achieve annual sales goals within defined territory/accounts through development, maintenance, and enhancement of customer accounts development, maintenance, and enhancement of customer accounts. Responsibility for managing all business accounts in assigned region/territory including implementing strategies in developing new growth of accounts. Drive the marketing process for the territory by creating a marketing plan, registering/planning/ attending local vendor shows, creating and working with Marketing and PM team to execute email campaigns | 4/4/2020 |
| 11747 | Biotechne Minneapolis, MN Laboratory Production Assistant HS Diploma/GED Exp: 0-2 years |
You will be responsible for assisting in the Clinical Controls Product Finishing Department with the bottling operation and the other activities involved in the product finishing process. Label product, operate the labeling equipment. Upon release of product by QA lab, count, verify and record number of finished products. Assist with monthly cleaning of clean room, including counters, laminer hoods, torque, labeler, sinks, and all work areas. | 4/4/2020 |
| 11748 | Biotechne Minneapolis, MN Administrative Support / Shipping Assistant HS Diploma/GED Exp: 0-2 years |
The responsibilities of this position are to support the DD OEM Accounts / Shipping Manager and Shipping Department’s activities by performing order processing, proofing, set assembly, shipping and other related duties. Order processing in our ERP System. Assist in preparing final shipping documents for OEM, International, Survey and Domestic shipments. Assist with maintaining Distributor, OEM and Survey customer orders and shipping records | 4/4/2020 |
| 11749 | Biotechne Minneapolis, MN Lab Assistant HS Diploma/GED Exp: 0-2 years |
The responsibilities of this position include processing raw biological materials for the use in manufacturing our products, maintaining and cleaning production equipment and containers, and completing required paperwork. Perform other duties as needed. Processes raw biological materials for the use in manufacturing our products. Maintains production equipment and containers | 4/4/2020 |
| 11750 | Biotechne Minneapolis, MN Research Associate, Cell Culture and Stem Cell Media Operations BS/BA in biological sciences Exp: 0-2 years in lab |
The main responsibility of this position it to maintain production of mouse embryonic fibroblasts. Additional responsibilities include media and supplement production, QC testing of methylcellulose-containing cell culture media, and cell culture of multiple cell lines. Perform additional duties as assigned. Preferred skills include cell culture, high attention to detail, strong communication and organizational skills. | 4/4/2020 |
| 11751 | Adarza Biosystems Maryland Heights, MO Manufacturing Technician BS to relevant sciences Exp: 0-2 years in pharma |
The position requires the ability to use and maintain delicate microarray equipment, training will be provided. Preferred candidates will have experience with laboratory automated systems, with a strong preference to individuals with silicon wafer processing and metrology systems (Cleaning, Etching, Optical Inspection and Ellipsometery) or experience in a related science discipline (biology, chemistry, biomedical engineering, or biochemistry). | 4/4/2020 |
| 11752 | Adarza Biosystems Maryland Heights, MO Manufacturing Technician BS to relevant sciences Exp: 0-2 years in pharma |
The position requires the ability to use and maintain delicate microarray equipment, training will be provided. Preferred candidates will have experience with laboratory automated systems, with a strong preference to individuals with silicon wafer processing and metrology systems (Cleaning, Etching, Optical Inspection and Ellipsometery) or experience in a related science discipline (biology, chemistry, biomedical engineering, or biochemistry). | 4/4/2020 |
| 11753 | Merieux NutriSciences Visalia, CA Laboratory Technician Micro AS/BS Exp: 1+ year(s) |
The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. Job Duties: Read plates and tubes, as required, to determine the number of organisms in the sample. Record findings on worksheet for verification. Write identification onto plates so that client and sample number can be tracked. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Prepare sample for analysis by recording, weighing, and blending. Collect plates and place them in the incubator for the specified amount of time and temperature. Prepare media and broth for use in pathogen testing as required. etc. | 4/1/2020 |
| 11754 | Merieux NutriSciences Crete, IL Customer Care Representative BS/BA Exp: 1+ year(s) |
Be the primary interface for customers. Is responsible for a select group of accounts with responsibility for properly setting up and welcoming them, ensuring proper and timely communications are in place, and timely resolution of issues. Acts as the liaison between Customers and our labs, Technical Sales Managers and other functions as needed and assist in identifying new opportunities with existing customers and ensure new leads are properly routed to the Sales function. Job Duties: Provide exceptional Customer Service while following Mérieux NutriSciences’ policies and best practices. Build and maintain productive collaborative relationships within the department and across the organization to effectively support the customer. etc. | 4/1/2020 |
| 11755 | Merit Medical South Jordan, UT Biological Safety Engineer I BS in biomedical engineering or related Exp: 1 year |
Performs biological safety related tasks and assists with biomaterials characterization and analysis in our R&D environment. DAY TO DAY: Assists with developing test strategies and test plans for biomaterials used in Merit Medical products. Assists with writing biocompatibility sections of 510(k)s, PMAs, IDEs, etc. for regulatory submissions, both in the U.S. and global markets. Assists with writing no-test rationales for well known and understood biomaterials. Maintains database of scientific literature references and testing. Works with R&D teams and engineers. etc. | 4/1/2020 |
| 11756 | Merit Medical South Jordan, UT Technician II AS/AA Exp: 1 year |
Performs routine technical tasks including assembling or constructing simple or standard equipment or parts, and may service or repair simple instruments or equipment. ESSENTIAL FUNCTIONS PERFORMED: Conducts a variety of tests using established and clearly defined methods. Prepares test specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Extracts engineering data from various prescribed sources and processes the data following well-defined methods, then presents the data in prescribed form. etc. | 4/1/2020 |
| 11757 | Merit Medical South Jordan, UT Molding Operator II HS diploma or equivalent Exp: 1 year |
This position is responsible for cosmetic part quality, dimensional charting, paperwork completion, and submission of molded component lots to Quality Assurance for final audit approval. ESSENTIAL FUNCTIONS PERFORMED: Performs start-up dimensions, as required. Submits daily lots to Quality Assurance for final audit. Packages and weighs the product and makes labels. Completes paperwork. Inspects parts visually and using measuring tools; documents results and ensures compliance to drawings and specifications; performs testing of products, as required. etc. | 4/1/2020 |
| 11758 | Meso Scale Diagnostics Gaithersburg, MD Research Associate I, Immunoassay Development BS in a life science Exp: 1+ year(s) |
A Research Associate I (RA I) is responsible for carrying out reagent and assay development activities in the laboratory, under supervision, working to achieve development project goals including data analysis and assay qualification. This is a laboratory position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). Some degree of professional latitude, creativity and self management is expected. DUTIES AND RESPONSIBILITIES: Analyze and prepare reagent and product documentation, organize and procure reagents, perform experiments, analyze data and document results. Presentation of results. Participation in general lab maintenance including maintaining laboratory supplies and equipment. etc. | 4/1/2020 |
| 11759 | Meso Scale Diagnostics Gaithersburg, MD Cell Culture Specialist I BS in biology, chemistry, engineering or related Exp: 6+ month(s) |
Lab & Equipment: Manage and manipulate multiple cell lines (both adherent and suspension), which are primarily high maintenance mouse hybridoma cell lines for the production of monoclonal antibodies and other cell based products. Execute transfections for the production of recombinant QRM antibodies. Use, maintain and troubleshoot the following cell culture equipment: Hemocytometer, Biological Safety Cabinet, Automated Cell Counter, Plate Readers (for ELISA and BCA assays), LN2 Freezers, Humidified Incubators, Water Baths, CO2 Tanks, and Controlled Rate Freezer. Use, maintain and troubleshoot AKTA purification systems. Occasionally handle BSL2 reagents. Provide general cell culture laboratory maintenance. Keep process areas stocked with essential equipment and supplies. etc. | 4/1/2020 |
| 11760 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Manuf BS in engineering or related Exp: 1+ year(s) |
In this entry-level position, the candidate will develop and implement optimal, cost-effective manufacturing processes and methods in accordance with product specifications and quality standards; this will include recommendation for and implementing improvements to production designs, tools/fixtures, processes, methods and controls. The incumbent will coordinate and/or assist manufacturing launch for new or revised products. DUTIES AND RESPONSIBILITIES: Develop and implement optimal, cost-effective manufacturing processes and methods for company products in accordance with product specifications and quality standards. Recommend and implement improvements to production designs, processes, methods and controls. Coordinate the manufacturing launch of new/revised products including establishing goals, generation of assembly documentation, training of team members and evaluating results. etc. | 4/1/2020 |
| 11761 | Analytical Lab Group Concord, CA Sample Receiving Technician HS diploma or equivalent Exp: 0-1 year |
The Sample Receiving Technician performs tasks such as Certificate of Analysis preparation, sample pickup and sample log-in. Technical support is performed in accordance with standard operating procedures and adheres to documentation practices in accordance with ALG-West policies. Sample Receiving personnel are responsible for reporting any adverse or unusual events to management, as well as participates in process improvement activities as needed. etc. | 4/1/2020 |
| 11762 | Analytical Lab Group Concord, CA Virology Associate BS in a biological science or related Exp: 1+ year(s) |
The Virology Associate is responsible for sample chain of custody, sample processing, testing and data reporting using a variety of virology, cellular and molecular biology methods and techniques. The position requires excellent organizational skills along with good written and verbal communication skills in English. Testing is performed in accordance with standard operating procedures. The Virology Associate is capable of the following work tasks with minimal supervision: Maintains working knowledge of lab equipment and methodologies necessary to monitor operation and service condition of equipment. etc. | 4/1/2020 |
| 11763 | Analytical Lab Group Concord, CA EM Technician AS/BS Exp: 1+ year(s) |
Analytical Lab Group is looking for laboratory technicians to perform environmental monitoring at client facilities and microbiology testing in the microbiology lab. This is a full-time position at our West Coast location. The schedule will be Monday-Friday, 7 a.m. to 3:30 p.m., but you must be able to work flexible hours, including different shifts and weekends. At this time, the starting hour is 5 a.m. and will require OT. Duties: Perform air sampling in cleanroom or laboratory areas. Collect and test microbial and chemical water samples. Collect and test compressed gas samples. Chemical cleaning and sanitization of equipment. etc. | 4/1/2020 |
| 11764 | Midwest Institute for Clinical Research Indianapolis, IN Medical Research Study Coordinator unspecified Exp: 1-3 year(s) |
We are seeking an experienced individual who has coordinated the implementation of clinical research protocols. 1-3 years of clinical research experience and CCRC certification is preferred for this full-time position. | 4/1/2020 |
| 11765 | Midwest Institute for Clinical Research Indianapolis, IN Medical Research Coordinator Associate unspecified Exp: 1-3 year(s) |
We are seeking an experienced individual who has been involved in clinical research. 1-3 years of clinical research experience is preferred for this full-time position. | 4/1/2020 |
| 11766 | MRIGlobal Kansas City, MO Associate Scientist, In Vivo MS Exp: Not necessary for MS candidates |
MRIGlobal’s Global Health and Security (GHS) Operations, Medical Countermeasures (MCM) Division is looking for an experienced Junior Scientist at our Kansas City headquarters. The Associate Scientist will provide technical project leadership and technical guidance to junior staff. The primary responsibilities of the position are: Serve as a Study Coordinator/Study Director for studies conducted in MCM (i.e. including Toxicology, Animal Health, and Biological and Chemical containment) and as a resource on animal models. Serve as a point of contact for clients and represent MRIGlobal. Provide technical guidance and direction to ensure the group meets and achieves project milestones. Provides leadership and training to technical staff on procedures and instrumentation. Helps to establish a course of action to accomplish a specific project or goal; plans proper assignments of personnel and appropriate allocation of resources; determines schedule of events; communicates expectations about tasks and deadlines; develops contingency plans. etc. | 4/1/2020 |
| 11767 | MRIGlobal Kansas City, MO Electrical Engineer MS Exp: Not necessary for MS candidates |
MRIGlobal has an exciting full-time opportunity for an Associate Electrical Engineer in our Intelligence, Surveillance, and Reconnaissance Division located in Kansas City, MO. In this unique opportunity, the selected candidate will work with other engineering and technical disciplines in the design, prototyping, and testing of custom systems to meet customer requirements. Furthermore, the selected candidate will: Design a broad range of analog and digital circuits. Design and layout custom circuit boards to meet challenging packaging and performance requirements. Design, layout, and assemble control and power distribution panels for custom systems. etc. | 4/1/2020 |
| 11768 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, biochemistry, chemical engineering or related Exp: Not necessary for BS/BA candidates |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Safely perform operations to meet quality expectations. Ensure quality throughout the process. Assure you are adequately trained to perform tasks/assignments. Perform routine assays, processes and/or unit operations. Complete the volume of work required to achieve group/departmental goals and meet deadlines. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). etc. | 4/1/2020 |
| 11769 | Mirati Therapeutics San Diego, CA Clinical Trial Associate BS in a scientific or healthcare field Exp: 1-3 year(s) |
We are seeking a highly motivated individual to join Mirati Therapeutics as a Clinical Trial Associate (CTA) within the Clinical Science/Operation Teams, reporting into a Director of Clinical Science. The CTA will interact with Clinical Science/Operation teams and collaborate effectively with CROs and vendors. The CTA supports the timely conduct of clinical studies according to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and all applicable regulations governing the conduct of clinical trials. etc. | 4/1/2020 |
| 11770 | Mizuho San Antonio, TX Field Service Engineer AS/AA in an electrical or applied science Exp: 1-2 year(s) |
The Field Service Engineer (FSE) is primarily responsible for technical support, repairing and servicing Mizuho products in the field throughout the United States. The Field Service Engineer provides, highly visible, customer support through the performance of independent on-site service and repair of complex equipment and systems. To include but not limited to installation, troubleshooting, repair, and performance of preventive maintenance as required. Responsible for the inspection and operational quality and safety of Mizuho OSI products. May also instruct customers in the operation and maintenance of the system. Serves as company liaison with customers on administrative and technical matters for assigned projects. Interprets customers’ needs and assigns the responsibility for problem resolution to the appropriate resource. etc. | 4/1/2020 |
| 11771 | Moderna Cambridge, MA Sr./Research Associate, Rare Diseases Research BS/MS in biology, biochemistry, molecular biology or related Exp: 0-3 years |
Moderna is seeking a self-motivated and adaptable Research Associate/Sr. Research Associate with experience in performing in vitro and in vivo analyses to support the development of novel mRNA therapeutics. The candidate will support preclinical and clinical programs through the development and execution of biological and bioanalytical assays, and interface with internal as well as external partners and collaborators. This position will contribute to the Rare Diseases therapeutic area through the performance and development of laboratory-based assays for early research through development candidates of novel therapies. The individual will work with scientists within Rare Disease and other parts of the company to ensure the highest level of quality of the work. etc. | 4/1/2020 |
| 11772 | Moderna Norwood, MA Research Associate, Pilot Development Lab BS in a life science or engineering Exp: 1-3 year(s) |
Moderna is seeking a Research Associate for the Pilot Development Lab, based at their Norwood, MA site. The individual in this role will be part of a cohesive team responsible for producing Drug Substance, Drug Product and Sterile Fill production for development and toxicology. The successful candidate must demonstrate the ability to quickly master new processes and must have the drive to be part of a dynamic, fast paced, and highly motivated team. Ideally, the candidate will have training in chromatography, TFF, aseptic and sterile drug product filling techniques and proven ability to work with custom automation. This position will require excellent communication and organizational skills, as well as a focus on operational excellence and process optimization. Candidates are expected to collaborate between technical development groups, Preclinical, GMP Manufacturing and Supply chain. etc. | 4/1/2020 |
| 11773 | Moderna Norwood, MA Sr/Research Associate, Process Development BS in chemical engineering, chemistry, or related Exp: 0-3 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. Moderna is seeking a highly skilled and motivated process development research associate residing in Moderna’s Technical Development organization. This role will support the process development of Moderna’s first-in-class messenger RNA (mRNA) based medicines to enable our clinical supply. The applicant should have strong communication and collaboration skills, along with multiple examples of a strong technical background. The successful candidate must be able to work in a fast paced and highly dynamic environment, will have relevant academic and or industrial experience in large molecule bioprocessing, and will be able to contribute to both process development and commercialization related activities. etc. | 4/1/2020 |
| 11774 | Moderna Norwood, MA Sr/Research Associate, Analytical Development MS in biophysics, cell biology, chromatography or related Exp: 1 year |
Moderna is seeking a Research Associate/Sr. Research Associate for a position based at their Norwood, MA site. The individual in this role will be a highly skilled, talented and motivated analyst. He/she will participate in performing biochemical and biophysical characterization (HPLC, cIEF, light scattering, particle characterization, spectroscopy, calorimetry) of lipid nanoparticles, lipids and mRNA. He/she will also participate in the coordination of characterization/comparability studies and compile the data packages into reports to support advancement of Moderna’s development candidates. The individual will work with other RAs and Scientists within the Analytical Development, Analytical Operations, and Platform Analytics teams. etc. | 4/1/2020 |
| 11775 | Moderna Norwood, MA Sr. /Research Associate, Molecular Biology BS/MS in molecular biology, biochemistry, chemical engineering or related Exp: 1-3 year(s) |
Moderna is seeking a curious, detail-oriented research associate for a position based at their Norwood, MA site. The individual will participate in the synthesis and analysis of research scale material using novel processes in support of Moderna’s mRNA platform. Here’s What You’ll Do: Synthesize mRNA at different scales to support research activities throughout Moderna. Develop and apply novel processes for mRNA synthesis. Perform analyses using various types of instrumentation (HPLC, mass spectrometry, etc.). Perform research to support new assays and process improvements. Maintain scientific records of experiments and clearly communicate results. Maintain a clean and organized lab bench. Maintain equipment and instruments. etc. | 4/1/2020 |
| 11776 | Moderna Cambridge, MA Sr./Research Associate, Process Development BS in chemical engineering, chemistry, or related Exp: 0-3 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. Moderna is seeking a highly skilled and motivated process development research associate residing in Moderna’s Technical Development organization. This role will support the process development of Moderna’s first-in-class messenger RNA (mRNA) based medicines to enable our clinical supply. The applicant should have strong communication and collaboration skills, along with multiple examples of a strong technical background. The successful candidate must be able to work in a fast paced and highly dynamic environment, will have relevant academic and or industrial experience in large molecule bioprocessing, and will be able to contribute to both process development and commercialization related activities. We seek applicants that are proactive, enthusiastic, and show a passion for process development. etc. | 4/1/2020 |
| 11777 | Moderna Cambridge, MA Workday Associate unspecified Exp: 1 year |
Reporting to the Manager, Human Resources you will be responsible for supporting our HR Workday needs and processes. Are you someone who loves supporting business processes and pulling reports? Do you want to work in a highly digitalized environment? Do you enjoy simplifying people processes with technology? Then Moderna is the place for you. We are seeking someone who has previously used Workday and is a fantastic communicator. This person must understand that successful business processes within Workday matter and that these processes are integral to the success of Moderna! Here's What You’ll Do: Partner with the HR team to understand their Workday needs. Help optimize Workday Business Processes, so they are simple and easy to understand. etc. | 4/1/2020 |
| 11778 | Molecular Templates Austin, TX Manufacturing Associate - GMP Upstream (2nd Shift) AS in a life science or engineering Exp: 1+ year(s) |
Molecular Templates is seeking an energetic and highly motivated professional to support upstream processing of therapeutic proteins. This position will perform functions related to production and GMP manufacturing operations, including execution of protein fermentation steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. etc. | 4/1/2020 |
| 11779 | Molecular Templates Austin, TX Manufacturing Associate - GMP Upstream (1st Shift) AS in a life science or engineering Exp: 1+ year(s) |
Molecular Templates is seeking an energetic and highly motivated professional to support upstream processing of therapeutic proteins. This position will perform functions related to production and GMP manufacturing operations, including execution of protein fermentation steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. etc. | 4/1/2020 |
| 11780 | Molecular Templates Austin, TX Manufacturing Associate - GMP Downstream (2nd Shift) AS in a life science or engineering Exp: 1+ year(s) |
Molecular Templates is seeking an energetic and highly motivated professional to support downstream processing of therapeutic proteins. This position will perform functions related to production and GMP manufacturing operations, including execution of protein purification steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. etc. | 4/1/2020 |
| 11781 | Molecular Templates Austin, TX Manufacturing Associate - GMP Downstream (1st Shift) AS in a life science or engineering Exp: 1+ year(s) |
Molecular Templates is seeking an energetic and highly motivated professional to support downstream processing of therapeutic proteins. This position will perform functions related to production and GMP manufacturing operations, including execution of protein purification steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. etc. | 4/1/2020 |
| 11782 | Molecular Templates Jersey City, NJ Clinical Trial Assistant BS in a life science Exp: 1+ year(s) |
Molecular Templates is seeking a highly-motivated and skilled professional to assist the Clinical Operations team. The Clinical Trial Assistant will provide support through maintenance of clinical trial studies. This includes establishing and maintaining the trial master file structure for all ongoing studies, providing coordination of supplies and inventory, coordinating meetings and preparing materials and ongoing general administrative support. This position requires excellent technical, analytical, time management and organizational skills, along with adherence to written and verbal instructions and accurate and timely completion of documentation. This position requires excellent organizational, time management and multi-tasking skills, along with the ability to follow standard operating procedures and manage competing priorities. etc. | 4/1/2020 |
| 11783 | Mylan Morgantown, WV Associate Electronic Submissions AS/AA Exp: 1+ year(s) |
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help: Performs moderately complex submission building, compilation, publishing and validation of receipt associated with generating hard copy and electronic (eCTD, NeeS, etc.) submissions to global health authorities. Prepares and completes a variety of simultaneous submission compilation activities including utilization of publishing tools (e.g. Lorenz docuBridge, ISIToolbox) for electronic and paper submission generation, scanning, QA/QC for document standards, and electronic/paper archiving. etc. | 4/1/2020 |
| 11784 | MyoKardia Brisbane, CA Scientist I, Pharmacology MS in physiology, pharmacology, biochemistry, or related Exp: 0-2 years |
ESSENTIAL DUTIES AND RESPONSIBILITIES: Work with colleagues in pharmacology to gain an understanding of primary and secondary pharmacologic mechanisms, biomarkers, translational potential, and safety for discovery- as well as development-stage programs. Implement appropriate clinically-relevant in vivo small animal models to study cardiovascular physiology and pharmacology. Design, execute, and summarize results from studies with novel small molecules that demonstrate detailed proof of mechanism. Establish PK/PD relationships in non-clinical species. Conduct and document studies to support proposed clinical indications (i.e. combination studies, label expansion). Serve as a pharmacology representative for cross functional project teams. etc. | 4/1/2020 |
| 11785 | NAMSA Irvine, CA Microbiolgy Technologist BS/BA Exp: No experience necessary for BA/BA candidates |
Principal Duties and Responsibilities: May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. May be required to operate autoclave, depyrogenation oven or other specified laboratory equipment. etc. | 4/1/2020 |
| 11786 | NAMSA Brooklyn Park, MN Animal Care Technician HS diploma or equivalent Exp: 0-2 years |
Principal Duties and Responsibilities: Primarily involved in the welfare and husbandry activities of animals, including sanitation of equipment and the vivarium. Receives, identifies, and acclimates laboratory animals. May euthanize animals. May administer medications under the direction of a Veterinarian. Follows the Quality Manual, all NAMSA SOPs, and Process documents. Documents all required tasks. May administer treatments as directed by staff veterinarian. etc. | 4/1/2020 |
| 11787 | NAMSA Northwood, MA Animal Care Technician HS diploma or equivalent Exp: 0-2 years |
Principal Duties and Responsibilities: Primarily involved in the welfare and husbandry activities of animals, including sanitation of equipment and the vivarium. Receives, identifies, and acclimates laboratory animals. May euthanize animals. May administer medications under the direction of a Veterinarian. Follows the Quality Manual, all NAMSA SOPs, and Process documents. Documents all required tasks. May administer treatments as directed by staff veterinarian. May conduct training on husbandry tasks for other Associates and update training records. etc. | 4/1/2020 |
| 11788 | NAMSA Northwood, MA Chemist MS Exp: No experience necessary for MS candidates |
Principal Duties and Responsibilities: Independently conduct testing according to written instructions. May be requested to conduct more involved studies. May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. May conduct routine testing per NAMSA SOPs as well feasibility, protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP, etc. Works with management to ensure large studies are completed on or before the due date. Prepare and maintain the reagents required for testing. May mentors and train staff in general laboratory testing as well as offering more complex instrumentation training. etc. | 4/1/2020 |
| 11789 | Merck KGaA Urbana, IL Production scientist, associate BS/BA in chemistry, biochemistry, chemical engineering or related Exp: Not necessary for BS/BA candidates |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Safely perform operations to meet quality expectations. Ensure quality throughout the process. Assure you are adequately trained to perform tasks/assignments. Perform routine assays, processes and/or unit operations. Complete the volume of work required to achieve group/departmental goals and meet deadlines. etc. | 4/1/2020 |
| 11790 | Merck KGaA Carlsbad, CA Quality Analyst 1 BS/BA in life sciences Exp: 1 year |
As a Quality Analyst 1, you will support the comprehensive quality activities, including entering, tracking and trending Environmental Monitoring (EM) data, managing timelines while ensuring the production environment is in a state of readiness. The role will entail operating in a fast-paced, highly dynamic environment with multifunctional groups/departments, including both internal and external stakeholders as needed. As a Quality Analyst, you will support the daily operations of the Microbiology/EM and Manufacturing processes and fills. You will need to complete documentation, data entry, and data review for EM data in a timely manner. Ensure that all required documentation including records and log books, is complete and entered in the timely manner and accurate according to the current GMP rules. etc. | 4/1/2020 |
| 11791 | Miltenyi Biotec Gaithersburg, MD Accounting Associate - Accounts Payable AS/AA Exp: 1-3 year(s) |
As a member of the Miltenyi Biotec Accounting team, you will work closely with Accounting leadership to assist in a variety of accounting functions focused on Accounts Payable. Your duties would include reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. You will use your collaborative nature to effectively coordinate intercompany communications and transactions with various departments, with management, and the parent company to enable the continuous success of Miltenyi Biotec as a whole. etc. | 4/1/2020 |
| 11792 | Miromatix Eden Prairie, MN R&D Operations Technician HS diploma or equivalent Exp: 1-2 year(s) |
Miromatrix is a biotechnology company on a mission to save and drastically improve countless lives by eliminating the organ transplant waiting list. Through our proprietary perfusion decellularization and recellularization technology, we are bioengineering human livers and kidneys to solve the large unmet clinical need that exits today. Miromatrix has an immediate opening for a highly motivated R&D Operations Technician at our Eden Prairie, MN facility. Primary duties include: Works with facility manager/supervisor to ensure clean room facilities are cleaned according to cGMP requirements. Performs various support functions using proper procedures to meet cGMP cleaning requirements. Maintains and cleans equipment and the facility; maintains and restocks supplies; strong attention to detail is essential while dealing with multiple tasks. Additional cleaning (i.e.,emergency cleanups, construction cleanups, and room set-ups) will need to be performed on an as needed basis. etc. | 4/1/2020 |
| 11793 | Aiomed Danvers, MA Clinical Research Associate I BS/BA in life sciences Exp: 1 years in field monitoring |
Reporting to the Manager of Clinical Research Associates, the person in this role is responsible for the management of day-to-day aspects of investigational site activities on assigned clinical trials. The CRA should ensure compliance with international guidelines, local regulations and corporate policies and procedures. Conduct reviews of documentation needed for internal and external audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Abiomed internal SOPs, and US and OUS regulations | 3/29/2020 |
| 11794 | AbSci Vancouver, WA Purification - RA I/II BS or MS in biochemsitry Exp: 1+ years in industry |
The Research Associate I/II will join our purification team and will play a significant role in purification of protein biologics. Core responsibilities include maintaining and operating chromatography instrumentation, (e.g., AKTA Pure, HPLC, etc.),conducting hands-on research for development of new techniques, and supporting ongoing protein purification activities. Develop and execute techniques to extract and purify protein biologics from SoluPro, AbSci’s proprietary E. coli expression platform | 3/29/2020 |
| 11795 | Accelerate Diagnostics Tucson, AZ Research Associate, Quality Control BS in chemical/biological sciences Exp: 1+ years in lab/research |
The Research Associate for Quality Control (QC) is a key member of the Operations Team under the direction of the Team Lead for Consumable Quality Control. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, HPLC-MS, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. | 3/29/2020 |
| 11796 | Accelerate Diagnostics Tucson, AZ Manufacturing Technician HS Diploma/GED Exp: 1 year in manufacturing |
The Manufacturing Technician will perform a variety of processing duties according to Batch Records (BRs) and Manufacturing Work Instructions (MWIs) in a cGMP environment for the Consumable Manufacturing Department including, but not limited to: Cleaning/recovery of classified area and work spaces, components preparation . Aseptic filling . Final Consumable Inspection | 3/29/2020 |
| 11797 | AccuraGEn Menlo Park, CA Research Associate/Senior Research Associate BS/MS in biological sciences Exp: 1+ years in industry/academia |
Plan, execute and interpret experiments; Analyze data, evaluate results, form conclusions, and recommend future experiments; Ensure accurate and consistent recording of experiment methods, materials and results; keep a high-quality laboratory notebook; Communicate and work efficiently with other groups within R&D team; | 3/29/2020 |
| 11798 | Accuray Madison, WI Production Technician Associates Degree Exp: 1-3 years in manufacturing or engineering |
The Production Technician is responsible for producing and testing components by assembling parts and subassemblies in manufacturing that will allow Accuray to provide products that meet customer needs and in accordance with regulatory requirements. Prepares work to be accomplished by gathering parts, subassemblies, tools, and materials required per job order. Assembles components per work instructions and tests product as required using test equipment and fixtures. | 3/29/2020 |
| 11799 | Acell Columbia, MD Biotechnician HS Diploma/GED Exp: Entry LEvel |
This is an entry level position for a Biotechnician. Employee will carry out manufacturing practices in a cGMP biotechnical facility. The job involves the manual processing of porcine urinary bladders, which includes all aspects from collection of raw materials to packaging of the final product. Following training, work will be expected to be performed independently to a high degree of standard in biomaterial handling. | 3/29/2020 |
| 11800 | WCG Clinical Eden Prairie, MN Associate Project Manager BS/BA in realted Exp: 1 year in admin for client facing projects |
The Associate Project Manager, at our Eden Prairie, MN office location, is responsible for the oversight of the more complex day-to-day administration and organization of client projects (working closely with the Project Manager) to ensure that projects are delivered on time, within budget and according to the agreed upon scope of work. | 3/29/2020 |
| 11801 | Acorda Therapeutics Chelsea, MA Process Mechanic - HVAC HS Diploma/GED Exp: 0-2 years |
The Process Mechanic HVAC I is responsible for performing and documenting the required maintenance and monitoring of the facility, systems, and equipment in a cGMP facility. The required duties include preventative and corrective maintenance on the facility’s mechanical system, operation of the facility's HVAC, installation of new equipment, general plumbing, electrical work, building grounds work and other duties as assigned. | 3/29/2020 |
| 11802 | Aurolife Pharma Dayton, NJ Warehouse Associate HS Diploma/GED Exp: 1 year in pharma warehouse |
It is the Warehouse Associate's responsibility to ensure that all cGMP material received (for example API, Excipients, & Packaging & Printing Components) are properly , accounted, stored and recorded as per cGMP requirements and standard procedures and to make sure all the ERP entries will be completed on time. 1. Receive materials and conform the information in the packing slip and issued P.O. 2. Store API, Excipient, Packaging and Printed components and other inventory controlled items on qualified location in the warehouse | 3/29/2020 |
| 11803 | Aurolife Pharma Dayton, NJ QA Documentation Associate BS/BA Exp: 1-2 years in GMP related industry |
Person will be responsible for the activities related to QA Documentation department related to Batch record issuance, Reconciliation of documents, Issuance of Control documents, file training record in company wide training folder of each employee. Maintain the Manufacturing and Packaging Batch Record Master Hard copy and Pdf soft copy. | 3/29/2020 |
| 11804 | Aurolife Pharma Lawrenceville, NJ Associate Chemist II BS in chemistry Exp: 1-3 years in pharma/analytical testing |
Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. Incumbent will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The incumbent may execute 95% - 100% of their work at the bench level. | 3/29/2020 |
| 11805 | Aurolife Pharma East Windsor, NJ Automation Engineer BS or MS in electrical/mechanical engineering Exp: 1-2 years |
The role of the AutomationEngineer is to ensure that all the Automated Storage and Retrieval System (ASRS), the associated features, and procedures of the Warehouse Control System are aligned and operational to ensure business continuity. The position works closely with key functional groups of Warehouse Operations and Projects to work on the new requirements and enhancements and take up continuous improvement projects to drive the operational efficiencies of the system. Apart from warehouse operations the position should work on the L3, L4 systems integration of DSCSA (Drug Supply Chain Security Act) Serialization requirements with the packaging team. | 3/29/2020 |
| 11806 | Acumed New York, NY Sales Associate - NYC BS in business/medical field Exp: 0-3 years in sales |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. Continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. | 3/29/2020 |
| 11807 | Acumed Hillsboro, OR Quality Assurance Technician 1 (Swing Shift) HS Diploma/GED Exp: 6-12 months in related |
The Quality Assurance Technician 1 (QAT) inspects in-process and finished materials and products, purchased or manufactured, to the required drawing or print specification, inspection plan or other controlling document. Documents out of specification situations by initiating nonconformance reports (NCMRs). Tests, inspects, or measures products, materials, and/or processes to evaluate conformance with specifications. | 3/29/2020 |
| 11808 | Abeona Therapeutics Cleveland, OH Associate, Inventory Control BS/BA in biological sciences Exp: 1 year in manufacturing |
The Inventory Control Operator is a critical role supporting the GMP Manufacturing, Process and Assay Development and Quality Control functions at Abeona. This individual will support and lead the organization and management of inventory encompassing the receiving, quarantine and release spaces. The ICO will ensure adequate inventories of all supplies (several hundred different SKUs) for Manufacturing during clinical trials, initial commercial process, for process and assay development activities, cleaning of Manufacturing facilities and gowning of Manufacturing associates. | 3/29/2020 |
| 11809 | Abeona Therapeutics Cleveland, OH Associate, Quality Control BS in biological sciences Exp: 0-4 years |
Abeona is looking for a Quality Control Associate to join our team in Cleveland, OH. The successful candidate is a key part of our growing QC Team and will be primarily responsible for performing routine laboratory activities in support of GMP testing for Quality Control. Testing includes raw material, packaging components, environmental monitoring, in-process and finished product. Interacts with employees internal and external to Quality Control. | 3/29/2020 |
| 11810 | Abzena San Diego, CA Lab Services Associate HS Diploma/GED Exp: 1 year in lab |
Provides maintenance of laboratory equipment. Maintains proper laboratory cleanliness and organization. Operates to the highest ethical and moral standards. Complies with Abzena’s policies and procedures.Adheres to all safety standards and protocols. | 3/29/2020 |
| 11811 | Aurolife Pharma East Windsor, NJ Manufacturing Operator Associates in engineering/STEM Exp: 1-3 years in batch manufacturing |
Manufacturing Associate is to perform all required Batch manufacturing, equipment cleaning, area cleaning, in- process testing & sampling for Manufacturing batches. Perform maintenance and troubleshooting of the equipment and machinery. Perform verifications using special instruments (pH meter, DO meter, Balance, etc.) Other Job Duties: Provide on-going technical support for manufacturing operations after project installation. | 3/29/2020 |
| 11812 | zPredicta San Jose, CA Laboratory Technician BS/BA in life sciences Exp: 0-1 years in lab |
To be successful, you have to be excited to support the fast-paced environment of a start-up, be engaged while performing multiple roles, and possess a desire to learn. Responsibilities include: Cell culture, Maintenance of lab safety records, Purchasing and procurement | 3/28/2020 |
| 11813 | Zymergen South San Francisco, CA Chemistry Associate, Polymer Characterization BS in polymer/material sciences Exp: 1-2 years in polymer characterization |
The ideal candidate has a strong technical background in polymer science with industrial materials R&D experience in polymer characterization. Familiarity with automation of data analysis and development of application testing for polymers is a strong plus. Execute our polymer characterization R&D efforts focused on our film products. Support lab safety, maintain and promote safe work practices | 3/28/2020 |
| 11814 | Zymo Research Irvine, CA Research Associate MS in life sciences Exp: 0-2 years |
The incumbent will have demonstrated clear leadership potential with ability to efficiently multi-task and manage a scientific research project, starting from the initial idea through to completion and publication in a peer-reviewed journal. Duties include: Assist in experimental design. Conduct complex, high-level scientific research activities. Interface with Principal Investigator to analyze experiments. Optimize experimental procedures. | 3/28/2020 |
| 11815 | Zymo Research Irvine, CA Customer Service Associate HS Diploma/GED Exp: 0-2 years |
The Customer Service Associate mainly processes orders via online, phone, fax, and emails. Other non- ordering job functions include interaction with customers to provide and process information in response to inquiries, concerns and requests about products and services. Receive and process customers’ orders - Main job function | 3/28/2020 |
| 11816 | Zymo Research Irvine, CA Technical Manufacturing and QC Associate BS in life/biological sciences Exp: 1-2 years in research |
Assist in the manufacturing of various chemicals, buffers, and other product-related components to ensure consistent product performance. Responsible for conducting quality control tests on various chemicals, buffers, and other product-related components. Initiate and implement appropriate experiments according to the SOP in order to accept or reject the release of product(s) and other related product components. | 3/28/2020 |
| 11817 | Zynex Medical Queens, NY Medical Device Sales 1121 - Addressing the Opioid Crisis BS/BA Exp: Previous sales experience a plus but not necessary |
We are seeking individuals who are self-confident, self-starting, resourceful, assertive, and persuasive. Must be able to build loyalty with clinicians and doctors developing a prescription-based stream of business. You will generate prescriptions from physical therapists and doctors for our NexWave pain management device, which is an alternative to opioid pain medication. This is an autonomous position that requires you to be independent and dedicated to becoming an outstanding medical device sales representative that services physical therapy clinics, pain management clinics, orthopedic surgical groups and other medical providers. | 3/28/2020 |
| 11818 | Zynex Medical Pasadena CA, Medical Device Sales 2027 - Addressing the Opioid Crisis BS/BA Exp: Previous sales experience a plus but not necessary |
We are seeking individuals who are self-confident, self-starting, resourceful, assertive, and persuasive. Must be able to build loyalty with clinicians and doctors developing a prescription-based stream of business. You will generate prescriptions from physical therapists and doctors for our NexWave pain management device, which is an alternative to opioid pain medication. This is an autonomous position that requires you to be independent and dedicated to becoming an outstanding medical device sales representative that services physical therapy clinics, pain management clinics, orthopedic surgical groups and other medical providers. | 3/28/2020 |
| 11819 | Zynex Medical Buena Park, CA Medical Device Sales 2038 - Addressing the Opioid Crisis BS/BA Exp: Previous sales experience a plus but not necessary |
We are seeking individuals who are self-confident, self-starting, resourceful, assertive, and persuasive. Must be able to build loyalty with clinicians and doctors developing a prescription-based stream of business. You will generate prescriptions from physical therapists and doctors for our NexWave pain management device, which is an alternative to opioid pain medication. This is an autonomous position that requires you to be independent and dedicated to becoming an outstanding medical device sales representative that services physical therapy clinics, pain management clinics, orthopedic surgical groups and other medical providers. | 3/28/2020 |
| 11820 | 10xGenomics Pleasanton, CA Research Associate – Sequencing Core BS/BA in biology/biochemistry or related Exp: 1-3 years in lab, qPCR, auto liquid handling systems |
We are seeking an experienced, collaborative and adaptable individual to join our 10X sequencing core team. The candidate will have a strong background in nucleic acid quantification and NGS workflows.Quantitation and QC of incoming sequencing libraries. Operate epMotion and other automated liquid handlers | 3/28/2020 |
| 11821 | 10xGenomics Pleasanton, CA Research Associate – Protein Engineering BS in biological sciences Exp: 1+ years in industry |
We are seeking a skilled and enthusiastic protein engineer at a Research Associate level to join the Protein Engineering Group. The candidate will be expected to work on a variety of protein engineering projects to optimize and generate differentiated enzymatic leads. Participate in protein engineering efforts to optimize various enzymes used in 10x Genomics products. Protein expression of various enzymes, preferably nucleic acid modifying enzymes. | 3/28/2020 |
| 11822 | 10xGenomics Pleasanton, CA Production Associate 1 BS or MS in biological sciences, chemistry, or engineering Exp: 1+ years in lab or QC of life science products |
Execute production operations according to defined procedures and ensure the integrity and quality of products. Operate liquid handling robotic system and complex manufacturing equipment for production biochemistry under supervision. Perform formulation and dispensing of reagent consumables and assemble into final kit configurations. Process work orders accurately using an ERP system in a timely manner | 3/28/2020 |
| 11823 | 10xGenomics Pleasanton, CA Process Engineer MS in life sciences/ engineering Exp: 1-3 years in lab |
10x is looking for an outstanding Process Engineer to join the Process Development team. This is a key position for the commercialization of consumable products associated with Next Generation Sequencing chemistries. This person will be responsible for developing and integrating process control and yield optimization solutions for complex reagent manufacturing workflows and identifying process to function relationships. | 3/28/2020 |
| 11824 | 4G Clinical Wellesley, MA Project Coordinator BS/BA in business administration or equal Exp: 0-2 years |
The Project Coordinator is an administrative professional who works with the Client Services Lead to ensure a project’s success. Monitor and communicate project status to team members. Organize and plan meetings. Communicate timeline changes and information to team | 3/28/2020 |
| 11825 | A2 Biotherapeutics Aqoura Hills, CA Research Associate MS in life sciences Exp: 1+ years in lab |
The Drug Discovery team is seeking a highly motivated individual with experience in cell and molecular biology. Molecular cloning, including construct generation and DNA/RNA preparations. Mammalian cell culture maintenance and cell-based assays. Design, execution, documentation and presentation of experiments | 3/28/2020 |
| 11826 | A2 Biotherapeutics Aqoura Hills, CA Research Associate MS in life sciences Exp: 1+ years in lab |
The Drug Discovery team is seeking a highly motivated individual with experience in cell and molecular biology. The successful candidate will join us at our research facility in Agoura Hills, CA and work on cutting edge science in a dynamic, fast-paced and team-oriented environment. Purification and biochemical characterization of recombinant proteins. Mammalian cell culture maintenance and cell-based assays | 3/28/2020 |
| 11827 | Abbott Plymouth, MN Operator I HS Diploma/GED Exp: 6 months or more in medical company |
We are seeking an experienced, high caliber Operator I. This position is responsible for the production of high quality medical devices within a manufacturing cell. This position includes detailed assembly and operation of various equipment and machinery. Ensure that relevant job documentation for cell operations and functions is accurate and up to date - Troubleshooting skills - Interpersonal skills such as conflict resolution, active participation, active listening, Interpreting, cooperation and flexibility to allow for a successful self-managed team | 3/28/2020 |
| 11828 | Abbott St. Paul, MN Quality Engineer I - Operations BS in engineering or technical field Exp: 0-2 years |
This position is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support. Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements. Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements | 3/28/2020 |
| 11829 | Abbott Alameda, CA Quality Assurance Specialist BS in engineering or life/physical sciences Exp: 1-2 years in pacing industry |
Working under direct supervision, provides education support to the Technical Service staff. Provides training to department for new hires, progression training, product launches, and field corrective actions. Provides periodic quality reviews of department calls and documentation. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercise judgment in planning, organizing and performing work; monitors performance and provides solutions for performance improvement. | 3/28/2020 |
| 11830 | Abbott Sylmar, CA Operator I HS Diploma/GED Exp: 6 months |
Briefly state the main purpose and scope of the job. Working under close supervision, may perform a combination of assembly, weld, x-ray, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies. Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed. | 3/28/2020 |
| 11831 | Abbott St. Paul, MN R&D Engineer, I BS in mechanical engineering, material science, or related Exp: 1-2 years in design/manufacturing |
The R&D Engineer I will use multidisciplinary engineering knowledge to contribute to a team designing and developing innovative medical devices or components/subsystems in the dynamic structural heart space where Abbott is a leading provider of solutions. Candidate will be responsible for providing engineering support in the creation and development of new medical device products as well as the support of established commercial medical device platforms in the heart valve space. | 3/28/2020 |
| 11832 | Abbott Sylmar, CA Electrical Development Quality Engineer I BS in electrical/system engineering, or physics Exp: 0-2 years |
Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs. Support and ensures the proper prediction of, and the ultimate product performance of the electrical system. Support on-time execution of Quality Plans for internal development, OEM-based and design change projects. Evaluates product design to identify potential design issues and drive technical decisions | 3/28/2020 |
| 11833 | Abbott Alameda, CA Complaint Investigation Technician HS Diploma/GED Exp: 1-2 years |
Safely perform routine testing and receiving of returned products due to customer complaints and be able to document investigation activities clearly and accurately in a timely manner. Adhere to procedures and work instructions throughout. Be able to handle multiple tasks effectively and efficiently. Understand the priorities of investigation as outlined in the procedures and as assigned by the laboratory supervisor. | 3/28/2020 |
| 11834 | Abbvie Lake County, IL Associate Scientist I/II, Engineering - Technical Operations BS or MS in chemical engineering Exp: 0-3 years |
This position will serve as a liaison between the Process Research and Development scientific functions and the API Pilot Plant organization. The successful candidate will assist in the optimization and scale-up of synthetic processes and facilitate the implementation of the processes and new technologies in to the API Pilot Plant. The Scientist will also provide technical oversight during production campaigns and will support technical transfer to the ultimate commercial manufacturing site. | 3/28/2020 |
| 11835 | Abbvie South San Francisco, CA Associate I/Associate II, In Vivo Pharmacology BS or MS Exp: 0-3 years in industry |
We are looking for an Associate Scientist I/II with experience in in vivo pharmacology study execution, start to finish including tumor implantation, data collection, and data analyses. Additional opportunities to learn new skills and to work on ex vivo lab experiments will be provided based on project need and candidate’s interest. | 3/28/2020 |
| 11836 | Abcam Cambridge, MA Logistics Technician HS Diploma/GED, BS/BA preferred Exp: Entry Level |
Process incoming shipments from suppliers, ensuring accuracy of all product data. Aliquot product into vials and assemble kits for customer orders and global stocking. Work with colleagues across the business to resolve discrepancies quickly. Maintain accurate inventory levels using both manual and automated systems. Fulfill customer orders using internal systems and processes, ensuring accuracy of all products in all orders. | 3/28/2020 |
| 11837 | Abcam Cambridge, MA Lab Technician - Protein Scientist Associates Degree Exp: 1 year |
Abcam is looking for a Lab Technician to join our team in Cambridge MA, working to support the Protein Science team in the development of standalone recombinant products at Abcam. Perform routine laboratory tasks, including glass wash, autoclaving, media and buffer preparation, centrifugation, ordering/inventory management, and vialing/labeling of protein samples. Communicate clearly with team members within the Protein Sciences Group, providing delivery dates and the necessary documentation as for activities. | 3/28/2020 |
| 11838 | Abcam Milpitas, CA Molecular Research Associate BS in molecular sciences or related Exp: 1 year in lab |
Following the acquisition of gene editing platform and oncology product portfolio of Applied StemCell Inc, we are now looking to expand the team as we look to become a leader in the cell engineering field. With this in mind, we are recruiting for a Research Associate to join our Molecular team. Conduct projects and experiments for genotyping and gRNA validation using multiple approaches, including PCR, Sanger sequencing, NGS, QPCR, ddPCR, Surveyor Assay, or any other assays as needed | 3/28/2020 |
| 11839 | Abcam Milpitas, CA Cell Science Research Associate BS in cell biology Exp: 1 year in lab |
Following the acquisition of gene editing platform and oncology product portfolio of Applied StemCell Inc, we are now looking to expand the team as we look to become a leader in the cell engineering field. With this in mind, we are recruiting for a Research Associate to join our Cell Engineering team. Perform cell engineering using CRISPR technology for service type cell-based projects. Generate and maintain modified cancer, iPSC and other cell lines in BSL-2 level laboratory environments | 3/28/2020 |
| 11840 | Abcam Eugene, OR Batch Production Research Associate BS in biological sciences Exp: 1 year in biotech |
Our facility in Eugene is responsible for the replenishment of a catalog of more than 2000 products for customers that expect high quality and a high degree of consistency between batches. Follow documented manufacturing work instructions. Comply with our Good Documentation Practices (GDP). Maintain physical and digital raw material, intermediate, bulk, and finished good inventory. | 3/28/2020 |
| 11841 | Abcam Branford, CT Research Associate BS in biological sciences Exp: 1-3 years lab experience |
The Custom Services Department is responsible for the development of best in class antibodies using wide variety of antibody discovery pipelines and extensive suit of antibody characterization assays. Execute experiments under direction of supervisorWork as part of the team to implement experimental plans support data management: ensure the recording and analysis of all processed data in a timely manner, with appropriate population of laboratory notebooks and data management systems | 3/28/2020 |
| 11842 | 3T Menlo Park, CA Research Associate MS in life sciences Exp: 0-2 years |
Protein engineering to support TCR-T cell programs, and identify compounds with optimal therapeutic index. TCR engineering for improved efficacy, and specificity. Performing cell-based assays to test prospective optimized leads. Discovery of TCR mimetic (mTCR) compounds that bind selectively to pMHC targets identified at 3T. Improvement of existing yeast display platforms and development of next-generation pMHC libraries. | 3/28/2020 |
| 11843 | MabPlex San Diego, CA Process Development Engineer/Associate MS in a science or engineering discipline Exp: 1+ year(s) |
This is an intermediate experienced engineer/associate position that will play an important role in developing stable cell lines and robust cell culture processes to be used in clinical manufacturing. Experience will dictate the exact title. The position will report to the Manager of Cell Line Development. Essential Job Responsibilities: Develop stable cell lines. Host cell transfection with target plasmid. Minipool screening and single-cell cloning. Shake flask fed-batch studies to support stability studies and top clone selection. etc.This is an intermediate experienced engineer/associate position that will play an important role in developing stable cell lines and robust cell culture processes to be used in clinical manufacturing. Experience will dictate the exact title. The position will report to the Manager of Cell Line Development. Essential Job Responsibilities: Develop stable cell lines. Host cell transfection with target plasmid. Minipool screening and single-cell cloning. Shake flask fed-batch studies to support stability studies and top clone selection. etc. | 3/25/2020 |
| 11844 | Mallinckrodt Pharmaceuticals Hobart, NY Packaging Operator I HS diploma or equivalent Exp: 3-12 months |
Packaging Line Operator is responsible for tending machines and conveyors at various stages of the packaging line to maintain efficient, continuous packaging of the product for shipment. Essential Functions: Components are in Place and Filled: Sets up assigned station(s) on the line including assembly of basic equipment and preparing materials needed (e.g. bottles, caps, cotton, etc.). Tends/operates station(s) during production run to insure proper operation and keep station filled with supplies or product. Weighs product at various stages of the packaging process. Performs checks/tests required for applicable station(s). Adjusts containers/materials for proper placement and remove defective pieces. Starts and stops equipment when required. Performs hand-packaging and material-handling functions. Collects all process related hazardous wastes and transports to accumulation drums. etc. | 3/25/2020 |
| 11845 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - C shift HS diploma or equivalent Exp: 3-12 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 3/25/2020 |
| 11846 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - D shift HS diploma or equivalent Exp: 3-12 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 3/25/2020 |
| 11847 | Mallinckrodt Pharmaceuticals Hobart, NY Manufacturing Assoc I - 3rd Shift HS diploma or equivalent Exp: 3-12 months |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 3/25/2020 |
| 11848 | Mallinckrodt Pharmaceuticals Hobart, NY Manufacturing Assoc I - 2nd Shift HS diploma or equivalent Exp: 3-12 months |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 3/25/2020 |
| 11849 | Matinas Biopharma Bridgewater, NJ Clinical Manufacturing Technician AS/AA Exp: 0-1 year(s) |
The Clinical Manufacturing Technician, LNC Manufacturing is responsible for the safe and compliant manufacture of clinical drug products as well as maintaining the manufacturing area in a clean, well supplied, and orderly state. The Clinical Manufacturing Operator, LNC Manufacturing Will Be Specifically Responsible For: Manufacturing of Clinical Supply Batches. Packaging and Labeling of Clinical Supply Batches. Following area Standard Operating Procedures. Cleaning of the Clinical Manufacturing Facilities and Equipment. etc. | 3/25/2020 |
| 11850 | MaxCyte Gaithersburg, MD Research Associate BS in a biological science Exp: 1 year |
The Research Associate is part of a team that works on cell loading technologies with applications that include gene and cell therapy and protein production. This individual executes a variety of laboratory procedures to ensure timely completion of the company's scientific objectives and customer requirements. This individual also provides lab support to scientists working with customers in the field. Works under general supervision. Job Duties: Performs general molecular techniques such as plasmid purification, gel-electrophoresis, DNA/RNA isolation, Western blot, Elisas, basic cell transfection experiments, and basic flow cytometry. etc. | 3/25/2020 |
| 11851 | McGuff Pharmaceuticals Santa Ana, CA Manufacturing Technician - Evening Shift unspecified Exp: Entry level |
McGuff Pharmaceuticals, Inc. currently has an opening for a Manufacturing Technician within our production facility located in Santa Ana, CA. This position reports to the Production Supervisor. The candidate must be detail-oriented, results-oriented, possess good communication and writing skills, capable of performing assigned production duties and flexible in adapting to changing work priorities. etc. | 3/25/2020 |
| 11852 | MedPace Cincinnati, OH Compensation Analyst BS/BA in business administration, accounting, human resources or related Exp: Entry level |
Medpace is a Clinical Research Organization (CRO) that is rapidly growing across the world. Due to our recent growth, we are in need of qualified and focused driven individuals, like yourself. This is a critical role in our continuously-growing Human Resources department, where you will be part of a dynamic, fast-paced work environment. As a Compensation & Benefits Analyst, you will be able to use your finely tuned skills to help accomplish task that are instrumental to the company’s growth. etc. | 3/25/2020 |
| 11853 | MedPace Cincinnati, OH Audit Associate AS/AA in a business related field Exp: Not necessary for AS/AA candidates |
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,700 people across 36 countries. etc. | 3/25/2020 |
| 11854 | MedPace Cincinnati, OH Automation Test Engineer unspecified Exp: 1+ year(s) |
Voted a Top Cincinnati Workplace for 4 years running, Medpace is growing rapidly, and we are currently seeking a full-time, office-based Software QA Tester to join our Information Technology (IT) team. The Software QA Tester position is a vital role whose success relies upon your knowledge, experience, and dedication. The Medpace IT department delivers software solutions that enable and empower both internal and external customers to manage their business processes most effectively and efficiently. Our Software QA Testers ensure these custom solutions are designed, built, and implemented correctly. etc. | 3/25/2020 |
| 11855 | LabCorp Burlington, NC Technologist (1st Shift) BA/BS in biology, chemistry, medical technology, or related Exp: 0-1+ year(s) |
We are seeking a Technologist to join our Reference Microbiology lab team in Burlington, NC! Performs tests and analyses according to established testing procedures in designated technical department. Assays performed in the in our department utilize a variety of scientific techniques, including Performs tests and analyses according to established procedures in designated technical department. Position may perform various techniques including EIA, IFA, and other non-automated and automated procedures. Open to entry level and senior level technologist's candidates as well as Technicians with an associates in Medical Laboratory Technology or Biotechnology. etc. | 3/25/2020 |
| 11856 | LabCorp Miami, FL Technologist [University of Miami] BA/BS in biology, chemistry, medical technology, or related Exp: 1 year |
Are you looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference? Are you an experienced Medical Lab Professional or desire to start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Miami, FL. In this position, you will work in a fast paced, customer focused, and challenging environment. etc. | 3/25/2020 |
| 11857 | LabCorp Winston-Salem, NC Medical Lab Technician - Float AS/AA in a laboratory science or medical technology Exp: 1 year |
Are you looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference? Are you an experienced Medical Lab Professional or desire to start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technician in Winston Salem, NC. In this position, you will work in a fast paced, customer focused, and challenging environment. etc. | 3/25/2020 |
| 11858 | LabCorp Burlington, NC Technologist (2nd Shift) BA/BS in biology, chemistry, medical technology, or related Exp: 0-1+ year(s) |
Are you looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference? Are you an experienced Medical Lab Professional or desire to start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in our Molecular Microbiology lab. In this position, you will work in a fast paced, customer focused, and challenging environment. Assays performed in the Molecular Microbiology area include Qualitative and Quantitative PCR, with the overall goal of providing results that can be used for the diagnosis and management of a wide range of infections using real-time PCR detection of nucleic acid. We are currently looking for someone who has or is looking to gain experience in PCR testing for this entry level Molecular Microbiology position. etc. | 3/25/2020 |
| 11859 | LabCorp Charlotte, NC ASCP Certified Medical Technician BA/BS in a laboratory science or medical technology Exp: 1 year |
Responsibilities: This is a clerical and processing position with no testing involved. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation. Demonstrate the ability to make technical decisions regarding testing and problem solving. etc. | 3/25/2020 |
| 11860 | LabCorp Burlington, NC Specimen Processing Specialist HS diploma or equivalent Exp: 1 year |
Job Duties/Responsibilities: Prepare laboratory specimens for analysis and testing. Spin samples, pour urine tubes, and create frozen samples. Unpack and route specimen to their respective staging areas. Accurately identify and label specimens. Pack and ship specimen to proper testing facilities. Properly prepare and store excess specimen samples. Process all necessary paperwork to process and submit specimen. etc. | 3/25/2020 |
| 11861 | LabCorp Houston, TX Technician AS/AA in a laboratory science or medical technology Exp: 1 year |
Are you looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference? Are you an experienced Medical Lab Professional or desire to start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technician in Houston, TX. In this position, you will work in a fast paced, customer focused, and challenging environment. The shift for this position will be Tuesday- Saturday 6 am to 2:30 pm. etc. | 3/25/2020 |
| 11862 | Merieux Nutrisciences Allentown, PA Microbiologist I unspecified Exp: 1-2 year(s) |
We are looking for a Microbiologist I. Responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. Follow appropriate methods and SOPS on all tasks. Maintain quality control records. Read, calculate, record data in Laboratory Information Management System. Perform rapid test methods. etc. | 3/25/2020 |
| 11863 | Merieux Nutrisciences Allentown, PA Lab Assistant unspecified Exp: No experience necessary |
The Technician we are looking for has… - The ability to work collaboratively, as a member of a team, to achieve a common goal. - A desire to protect themselves, their friends and family, and the entire world from illness caused by foodborne pathogens. - The flexibility and productivity to work in a fast paced, often varied environment. - A strong sense of pride in achieving accurate, timely, and consistent results in their work. etc. | 3/25/2020 |
| 11864 | Merieux Nutrisciences Columbus, OH Micro Tech unspecified Exp: Entry level |
We are looking for a Micro Tech. Your missions will be to: Prepare samples for processing and maintains documentation of process to facilitate analysis procedures. This position requires weekend work. The Laboratory Technician we are looking for has… - The ability to work collaboratively, as a member of a team, to achieve a common goal. - A desire to protect themselves, their friends and family, and the entire world from illness caused by foodborne pathogens. - The flexibility and productivity to work in a fast paced, often varied environment. - A strong sense of pride in achieving accurate, timely, and consistent results in their work. etc. | 3/25/2020 |
| 11865 | Merieux Nutrisciences Allentown, PA Microbiology Technician unspecified Exp: Entry level |
Prepares sample for processing and maintains documentation of process to facilitate analysis procedures. Job Duties: Read plates and tubes, as required, to determine the number of organisms in the sample. Record findings on worksheet for verification. Write identification onto plates so that client and sample number can be tracked. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Prepare sample for analysis by recording, weighing, and blending. Collect plates and place them in the incubator for the specified amount of time and temperature. etc. | 3/25/2020 |
| 11866 | Merieux Nutrisciences Madison, WI Microbiology Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. Your Mission: Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. etc. | 3/25/2020 |
| 11867 | Merieux Nutrisciences Stone Mountain, GA Micro Tech unspecified Exp: No experience necessary |
We are looking for a Micro Tech: The ability to work collaboratively, as a member of a team, to achieve a common goal. A desire to protect themselves, their friends and family, and the entire world from illness caused by foodborne pathogens. The flexibility and productivity to work in a fast paced, often varied environment. A strong sense of pride in achieving accurate, timely, and consistent results in their work. etc. | 3/25/2020 |
| 11868 | Mammoth Biosciences San Francisco, CA Research Associate - Genome Editing BS in a relevant field Exp: 1+ year(s) |
Mammoth is seeking a Research Associate with experience in tissue culture and genome editing. The ideal candidate will have experience working with genome editing technologies. Strong candidates for this role will also have experience with molecular biology and cloning. Understanding of CRISPR systems and their applications is a plus. Responsibilities: Work directly with Scientists and Research Associates to develop new CRISPR tools. Establish and maintain mammalian cell lines. Analyze genome editing outcomes with NGS and flow cytometry. etc. | 3/25/2020 |
| 11869 | Mammoth Biosciences San Francisco, CA Research Associate - Assay Development BS/MS in biology, chemistry, or related Exp: 1+ year(s) |
Mammoth is seeking a Research Associate experienced in protein and nucleic acid biochemistry techniques to support our research and product development teams. The ideal candidate will have experience with in vitro assay development, nucleic acid extraction and amplification techniques. Further, the candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. etc. | 3/25/2020 |
| 11870 | Maverick Therapeutics Brisbane, CA Research Associate, Cell Biology & Assay Development BS/MS Exp: 0-3 years |
This position will involve the development of in vitro assays to characterize lead clinical candidate molecules in drug development. It will primarily focus on developing both immunochemical assays and cell-based assays to support the development of preclinical pipeline products. Additional responsibilities may include testing early pipeline molecules in established in vitro assays and/or developing novel in vitro assays to support mechanism of action studies. Key Responsibilities: Execute assigned tasks following appropriate laboratory/technical procedures under minimal supervision. etc. | 3/25/2020 |
| 11871 | Lifecore Biomedical Chaska, MN Machine Operator I HS diploma or equivalent Exp: 6+ months |
The Machine Operator I is responsible for the setup and operation of standard packaging machinery in the packaging department. This includes working with and monitoring other packaging personnel to complete equipment set up and operation required by the department schedule. Machine Operators must comply with regulatory requirements, Good Manufacturing Practices (GMP), Standard Operating Procedures (SOP), and Manufacturing Process Records (MPR). They will perform all processes as required to fill, label, print, tray seal, pouch, final package, and inspect any Lifecore product; document completed work during packaging of final product; continually practice proper precautions and procedures when working with equipment and handling chemicals; etc. | 3/24/2020 |
| 11872 | Lifecore Biomedical Chaska, MN QC Microbiologist I BS in microbiology, biology, or related science Exp: 0-2 years |
This individual will ensure accurate, reproducible, and timely QC testing in support of manufacturing; support development, validation and stability studies on an as-needed basis; participate in methods improvements within the laboratory. They will perform testing on in-process product, final product, and raw materials for routine testing, validation testing, and stability testing; communicate results through appropriate documentation and batch records, statistical analysis and trending; acquire and maintain cleanroom and gowning qualification; participate in rotation to provide weekend and holiday coverage; perform instrument maintenance; identify and report equipment and method failures; identify areas for continuous improvement. etc. | 3/24/2020 |
| 11873 | Lipocine Salt Lake City, UT Associate Scientist BS/MS in a life science, chemical engineering, or related Exp: 1-3 year(s) |
Associate scientist needed in the area of pharmaceutical drug delivery research. Responsibilities include conducting laboratory experiments in support of formulation and process development. Qualified candidates will possess a BS/MS in life Science, chemical engineering or related field or 1-3 years experience in a pharmaceutical or chemistry laboratory. Knowledge of laboratory practices and demonstrated skills in analytical instrumental techniques (e.g. HPLC) are preferred. Excellent communication skills needed for preparing and following standard test methods and reporting experimental results. | 3/24/2020 |
| 11874 | Liquidia Technologies Morrisville, NC Associate Scientist BS in relevant scientific field Exp: 0-2 years |
This is a laboratory-based position where the candidate will have the opportunity to leverage Liquidia’s PRINT® technology in the development of new pharmaceutical products. In this role, the candidate will be responsible for supporting preclinical and early clinical formulation development focusing on inhalation powders. Specific Duties, Activities, and Responsibilities: Work with manager and team members to design and evaluate new product formulations. Use experimental design principles to optimize formulation composition and identify early manufacturing process. Support manufacture of material for formulation development as well as preclinical and early clinical studies. etc. | 3/24/2020 |
| 11875 | Liquidia Technologies Morrisville, NC Manufacturing Technician - Temporary to Permanent BS Exp: 0-2 years |
The Manufacturing Technician (Temporary to Permanent) will perform routine running of manufacturing equipment to support production and R&D efforts. This role will provide feedback to engineering and scientific staff on process performance and ideas for process improvement. Responsibilities: Responsible for running manufacturing equipment to support production and R&D efforts. Collect samples for in-process testing and complete test and inspection activities. Monitor the manufacturing process, recording observations and key run parameters as needed, and adjusting the process as necessary within the defined process window. etc. | 3/24/2020 |
| 11876 | Locus Biosciences Research Triangle Park, NC Research Associate BS/MS in microbiology, synthetic biology, genetic engineering, or related Exp: 6-24 months |
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Research Associate. This position is well suited for those that can accomplish defined work, as well as assist in approaching and solving complex scientific problems. This individual will be responsible for assisting in the generation, production and characterization of novel antimicrobial products. The ideal candidate will be able to independently conduct general microbiological and molecular biology research, and assist in the development of our broader research goals. This individual must be able to communicate effectively in formal and informal settings and be able to work well within a team. Candidates should have prior laboratory experience and be competent at basic molecular biology techniques. etc. | 3/24/2020 |
| 11877 | Locus Biosciences Research Triangle Park, NC Data Analyst BS/MS in bioinformatics, computational biology, or data science Exp: 6-24 months |
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Data Analyst. This individual will be responsible for assisting in the generation, production and characterization of novel antimicrobial products. Primary responsibilities include maintaining and leveraging data acquired from automated and high-throughput instruments. The ideal candidate will be able to drive the automation of data acquisition from lab instruments, maintain a data warehouse, and derive meaningful insights from large datasets. This individual must be able to communicate effectively in formal and informal settings and be able to work well within a team. Candidates should have a passion for data-driven decision making and bringing life-saving therapeutics to patients. etc. | 3/24/2020 |
| 11878 | LogicBio Cambridge, MA Animal Care Technician AS/AA in biology, pharmacology, or related Exp: Entry level |
LogicBio is seeking a highly motivated animal care technician to join our in vivo pharmacology group. The successful candidate will support preclinical development by ensuring the proper care of our research animals and assist in our vivarium operations. If you share our passion and sense of urgency for finding a lasting cure for patients, and are looking for a dynamic, collaborative and fulfilling work environment, we invite you to join our team. etc. | 3/24/2020 |
| 11879 | LogicBio Cambridge, MA Research Associate, Discovery Biology BS in biology, biochemistry, molecular biology, or related Exp: 1-2 year(s) |
LogicBio is seeking an entry level Research Associate to join our Discovery Biology team. The successful candidate will support the team in performing assays to assess protein expression and function of new targets in our growing pipeline. This role will work closely with other teams internally and externally, and support the analysis of preclinical studies to evaluate therapeutic candidates. Primary Responsibilities: Perform molecular and cellular-based assays to assess protein expression and activity. This includes, and is not limited to ELISAs, SDS-PAGE, BCA protein, and immunoblotting assays. Support assay development team in developing, optimizing and validating assays. Work closely with in vivo pharmacology and R&D teams to support sample analyses. Maintain and update detailed electronic notebook of experiments. Prepare, review and deliver scientific presentations for internal/external use. etc. | 3/24/2020 |
| 11880 | LGC Novato, CA GMP Manufacturing Technician BS/BA in a related field Exp: Not necessary for BS/BA candidates |
The GMP Manufacturing Technician I position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. Areas of Responsibility: Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director. Maintain batch records, equipment logs and other production records as directed per company procedures. Maintain a clean an orderly laboratory environment. Perform routine maintenance of equipment used in manufacturing. etc. | 3/24/2020 |
| 11881 | LGC Petaluma, CA Chemical Production Support Technician I College-level chemistry coursework Exp: Not necessary with coursework |
In our Genomics Division, we use our expertise in DNA extraction, genotyping, sequencing and PCR to enable scientists and companies to feed, cure and protect the world’s population. We supply genomic services from our UK, Germany and US laboratories, to global customers in agricultural biotechnology, molecular diagnostics, research, pharma/biotech, applied and clinical markets. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. etc. | 3/24/2020 |
| 11882 | LGC Manchester, NH Kitting Assistant I/Chemical Repackager I HS diploma/AS Exp: 0-1 year(s) |
The Production Department at LGC Standards in Manchester, NH produces an extensive line of analytical single and multi-element reference standards both in oil and aqueous matrices. The kitting group supports production by packaging standards used together in a kit. We are ISO 9001, ISO 17025, and ISO 17034 accredited. The main function of this role is to bottle and assemble private label kits in a clean and safe lab environment. The secondary function of this role is to package bulk product into finished goods bottle with the downstream production group. Key responsibilities and accountabilities: Label and package kits for private label customers. Clean labware and prepare vials/bottles per instructions. Repackage product from bulk containers to final product packaging as needed. Leak test final packages, apply labels and celoms, and check labels for accuracy. etc. | 3/24/2020 |
| 11883 | Xellia Pharmaceuticals Cleveland, OH Aseptic Operator II - All shifts available HS Diploma/GED Exp: 1-2 years in cGMP environment |
Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. | 3/22/2020 |
| 11884 | Xellia Pharmaceuticals Cleveland, OH Compliance Quality Assurance Specialist BS in life/physical sciences Exp: 1-5 years |
The Compliance Quality Assurance (CQA) Specialist is responsible for providing quality oversight to all Doc Control, Change Control, Deviation Management, APR’s, Auditing, Laboratory, Complaints, Reprocess, Recalls and Supplier Qualification to ensure product quality and SOP/GMP compliance at the Cleveland Manufacturing Facility. Works with the aforementioned departments to resolve all quality issues or escalate to the Quality Assurance Manager as appropriate, and ensure good documentation practices are being followed. | 3/22/2020 |
| 11885 | Xellia Pharmaceuticals Cleveland, OH Aseptic Operator I - All shifts available HS Diploma/GED Exp: 0-1 years in cGMP environment |
Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. | 3/22/2020 |
| 11886 | Xellia Pharmaceuticals Cleveland, OH Aseptic Operator, IV Bag Manufacturing II HS Diploma/GED Exp: 1-2 years in cGMP environment |
Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. | 3/22/2020 |
| 11887 | Xellia Pharmaceuticals Cleveland, OH Microbiologist - 2nd Shift BS/BA in sciences Exp: 0-2 years in lab |
In this role, the Microbiologist I is responsible for will be responsible for all aspects of the Microbiology laboratory operations, such as sample receipt, sample testing, data generation, data analysis and summarization and other QC lab supporting activities. Uses good documentation practices in the collection of data/records. Authors and executes qualification documents, SOPs, protocols, and investigations. | 3/22/2020 |
| 11888 | Xellia Pharmaceuticals Cleveland, OH Inside Sales Representative BS/BA Exp: 1-3 years in pharma/biotech/medical |
As a part of Xellia’s growing, energetic, and innovative pharmacy injectables Sales Team, the Inside Sales Representative will reach customers via telephone and sell our newly patented Vancomycin RTU IV bags to new customers. While meeting established individual and organizational sales objectives, the Inside Sales Representative will build and maintain valuable sales skills, cross-functionally learn about all facets of the business, and help develop a pathway for growth opportunities and career advancement. | 3/22/2020 |
| 11889 | Xellia Pharmaceuticals Cleveland, OH CCA Material Handler HS Diploma/GED Exp: 1-2 years, must be able to use forklift |
The CCA Material Handler is responsible for receiving, stocking, issuing, and delivering material required to support the Cleveland manufacturing operations. Responsible for receiving all items for this location and working with Warehouse and Quality to ensure all material is ready for production use. Locates product and material and transfers to CNC and CCA as applicable. Performs all transactions to confirm the issuance, transfer or destruction of materials that have been picked, transferred or destroyed. | 3/22/2020 |
| 11890 | Yokogawa Sugar Land, TX ESTIMATOR I BS in engineering or math Exp: <2 years experience |
Responsible for overall estimation and order processing activities associated with the successful completion of assigned Systems Parts quotations including technical and commercial review and compliance, product selection, costing and support to achieve the division’s short-range and long-term business objectives of providing accurate, timely and precise information for all customer quotations. | 3/22/2020 |
| 11891 | Yokogawa Newnan, GA ASSEMBLER I HS Diploma/GED Exp: 1 year in manfacturing/soldering |
To assemble product in accordance with shop orders and established production procedures. To produce a product in high quality by utilizing the necessary tools and equipment provided. Work using the NYPS philosophy and 6's. Have the ability to perform with speed and accuracy in all processes of the job. Determine type of instrument, parts necessary and production procedure to be followed for the required instrumentals by reading shop orders or work card. | 3/22/2020 |
| 11892 | Yokogawa Newnan, GA Rotational Engineer BS/BA in engineering Exp: Entry Level |
Yokogawa’s Emerging Engineering Talent Rotational Program is an 18 month program designed to grow high potential talent by accelerating their development through technical and professional training and different engineering assignments. The program is composed of three rotational assignments designed for its members to gain hands-on experience while working on challenging projects, and gaining leadership exposure through targeted training and intentional engagement with Subject Mater experts and organizational leaders. | 3/22/2020 |
| 11893 | ZeteoTech Sykesville, MD Electrical Engineer - Software Systems BS in electrical/computer engineering Exp: 1-5 years in data analysis/data sciences |
Actively participate in the design, development and implementation of data/information processing and analysis systems. Work with the Zeteo team and customers at all stages of the development process to ensure successful commercialization. Support development, implementation and testing of signal and information processing algorithms | 3/22/2020 |
| 11894 | ZeteoTech Sykesville, MD Electrical Engineer - Embedded Sensors BS in electrical/computer engineering Exp: 1-5 years in embedded systems |
The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. Actively participate in the design, development and implementation of embedded systems, including platform selection, programming, and testing. Work with the Zeteo team and customers at all stages of the development process to ensure successful commercialization. | 3/22/2020 |
| 11895 | ZeteoTech Sykesville, MD Chemist BS in chemistry Exp: 1-5 years |
Conduct chemical experiments, tests, and analyses using techniques such as MALDI-TOF mass spectrometry, gas chromatography mass spectrometry, and microscopy. Conduct chemical and physical laboratory tests to assist scientists in refining MALDI-TOF MS equipment. Compile and interpret results of tests and analyses. Prepare chemical solutions for products and processes following standardized formulas, or create experimental formulas | 3/22/2020 |
| 11896 | ZeteoTech Sykesville, MD Electrical Engineer BS in electrical/computer engineering Exp: 1+ year in embedded systems |
Our ideal candidate is interested in working in an entrepreneurial environment, developing game changing solutions to healthcare and national security challenges. You'll use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. | 3/22/2020 |
| 11897 | ZeteoTech Sykesville, MD Microbiologist BS/BA in biological sciences Exp: 1-5 years lab experience |
You will use your expertise to conduct biological laboratory tests to assist scientists in development of tools to detect and decontaminate biological organisms and materials. This is an entry-level position with room for growth. Prepare media and reagents required for conduct of microbiological analyses, while practicing aseptic techniques. Perform routine and non-routine sampling and testing of decontamination approaches. | 3/22/2020 |
| 11898 | Zimmer Biomet Irvine, CA Clean Room/ Packaging Operator AS/AA in biotech/med/life sciences Exp: 0-2 years |
Performs drug product formulation, filling, crimping, sterilization, Visual inspection, labeling and Packaging. May be required to perform all or a combination of the duties listed below. Buffered solution preparations according to Standard Operating Procedures (SOP’s). Chemical Reactions and RODI Purification of reaction precipitate. | 3/22/2020 |
| 11899 | Zimmer Biomet Warsaw, OH Quality Engineer BS in engineering Exp: 0-3 years |
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. Formulates procedures, specifications, and standards for Zimmer products and processes. Develops and implements corrective/preventative action plans. | 3/22/2020 |
| 11900 | Zimmer Biomet Scottsdale, AZ Quality Engineer BS in engineering Exp: 0-3 years |
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. Formulates procedures, specifications, and standards for Zimmer products and processes. Develops and implements corrective/preventative action plans. | 3/22/2020 |
| 11901 | Zimmer Biomet Memphis, TN Product Assur Coordinator (602436) - 2nd Shift position HS Diploma/GED Exp: 1-3 years mechanical inspection |
The Product Assurance Specialist is responsible for inspecting parts at all stages of processing (acceptance, clean, package, and label) and deciding whether or not the parts conform to visual and dimensional specifications and documenting these decisions and supporting data. The Specialist must work with minimal supervision and be capable of evaluating and judging level of conformance with defined requirements. | 3/22/2020 |
| 11902 | Zimmer Biomet Warsaw, OH Contract Associate Specialist BS/BA in business or related Exp: 0-3 years |
Responsible for administering and analyzing contracts with regional buying groups, medical surgical distribution companies, integrated health systems, and individual facilities while assisting with national group purchasing organizations. Thoroughly understands and applies good contract management principles. Administers contract maintenance process to ensure sales transactions are accurate and recorded timely. Strong analytical skills are required for position. | 3/22/2020 |
| 11903 | Zimmer Biomet Warsaw, OH Manufacturing Engineer BS/BA in engineering Exp: 0-3 years in engineering |
The manufacturing engineer is responsible for providing manufacturing engineering services to support efficient manufacturing processes. Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. Maintaining and improving controlled technical documents such as prints, procedures, bill of materials and routers. Supporting a wide variety of processing applications such as machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc. | 3/22/2020 |
| 11904 | Vividion San Diego, CA Research Associate, Molecular and Cellular Biology BS/MS in cell biology Exp: 0-3 years |
The successful candidate will have extensive hands on experience and expertise in basic molecular biology, mammalian cell culture techniques,and cellularand biochemical assay development. They will supportthe validation of novel drug targets via multiple mechanisms, including testing the effects of compounds on proteins in cellular and biochemical settings. They will utilize the development and/or use of new technology to support drug discovery. | 3/21/2020 |
| 11905 | Vodori Chicago, IL DevOps Engineer BS/BA in computer sciences/engineering Exp: 1-2 years in devops, system engineering/software develoment |
Our platform is based on open source technologies, so if you have a passion for Linux server administration (CentOS), Web server configuration (Apache & Tomcat), Database administration (MySQL & MongoDB), and Infrastructure management and automation (Puppet, Docker, and Kubernetes), you would be a great fit for this role. In this role, you will automate tasks using Python, Bash, or other scripting technologies. You will find it very helpful to have previous experience with AWS (Amazon Web Services) in cloud networking and working with SaaS software in cloud environments. | 3/21/2020 |
| 11906 | Voyager Therapeutics Cambridge, MA Research Associate, Vector Engineering BS in molecular/cellular biology Exp: 1-3 years in research |
This is an ideal position for an individual with experience in in vitro molecular biology assays, who thrives in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment. The individual will work in the laboratory and be responsible for experimental execution for research studies supporting cutting edge therapeutic programs and platform discovery research in neurodegenerative disease areas. We are looking for a candidate with hands-on experience with molecular clonings and downstream analysis (e.g. RT-qPCR, ELISA, tissue sectioning, immunohistochemistry and western blot). | 3/21/2020 |
| 11907 | Wake Research Las Vegas, NV Clinical Research Patient Recruiter HS Diploma/GED Exp: 0-2 years |
The Clinical Research Patient Recruiter will engage in community resources to identify, pre-screen and schedule subjects based on assigned studies by demonstrating a knowledge of study requirements and schedules. They are also responsible for maintaining a working knowledge of all actively-enrolling and upcoming trials. Engage in community resources, including but not limited to, social media, support groups and educational events. | 3/21/2020 |
| 11908 | Wake Research Raleigh, NC Clinical Research Patient Recruiter HS Diploma/GED Exp: 6 months in call center |
The Clinical Research Patient Recruiter will pre-screen and schedule subjects based on assigned studies by demonstrating a knowledge of study requirements and schedules. They are also responsible for maintaining a working knowledge of all actively-enrolling and upcoming trials. | 3/21/2020 |
| 11909 | Waters Milford Machining Milford, MA Quality Engineer I - Machining Operations BS in engineering Exp: 0-3 years in manufacturing |
Quality engineering support will include nonconformance management, process improvement, programming of automated inspection equipment, fixture design, and statistical analysis of process qualification data. The ideal candidate shall be comfortable communicating with machine operators, mechanical inspectors, process engineers, operations management, and quality systems staff, and shall possess knowledge of design and manufacturing principles. | 3/21/2020 |
| 11910 | Waters Golden, CO Assembly/Production Technician II - ASR HS Diploma/GED Exp: 0-2 years in quality |
This position will join a team which has responsibilities for production, assembly, inventory control, labelling, kitting, transporting, and Quality Control of products. It includes completing documentation and review to meet Waters Analytical Standards & Reagents (ASR)specifications. Quality and attention to detail are top priority. | 3/21/2020 |
| 11911 | Waters Milford, MA Electronics Technician AS/AA or apprenticeship Exp: 1 year as electronic technician |
This position involves performing all aspects of support, repair and maintenance to electrical/mechanical systems in a state-of-the-art Instrument development group. Record data with equipment such as a DVM, O-scopes, logic analyzers, and other electric measuring/monitoring devices. Collaborate with engineers and other professionals on technical tasks. Service, maintain and troubleshoot electrical problems on both new and legacy Water Liquid Chromatography (LC) systems. | 3/21/2020 |
| 11912 | WCCT Global Cypress, CA Clinical Research Technician Medical assistant or CPT1 Exp: 1 year clinical research experience |
The Clinical Research Technician (CRT) works directly with the Clinical Trial Director (CTD), Clinical Trial Manager (CTM), Clinical Research Coordinator (CRC), or Assistant Clinical Research Coordinator (ACRC) in the preparation, collection, compilation, and documentation of clinical research data by performing administrative and clinical duties. | 3/21/2020 |
| 11913 | Westat Rockville, MD Research Assistant BS/BA in social sciences/educaton Exp: 1 year in research or education |
We have an immediate opening for a research assistant who will work with a research team to support the data collection for the National Assessment of Educational Progress, (NAEP), an innovative digital educational assessment also known as “The Nation’s Report Card.” | 3/21/2020 |
| 11914 | Westat Rockville, MD Research Assistant BS/BA in social sciences Exp: 1-3 years in research |
Westat is seeking a research assistant with strong quantitative skills to contribute to education research and evaluation projects. Developing code in statistical software to manipulate data, produce descriptive statistics, and conduct inferential analysis (e.g., multiple regression). Creating data visualizations with Microsoft Excel or other tools. | 3/21/2020 |
| 11915 | Westat Rockville, MD Research Assistant BS/BA in social sciences/educaton Exp: 1 year working |
We have an immediate opening for a research assistant who will work with a multidisciplinary research team to support the data collection for the OECD’s Programme for International Student Assessment (PISA), the world’s largest international education assessment involving more than 85 countries and economies. | 3/21/2020 |
| 11916 | Westat Rockville, MD Research Assistant BS or MS in social sciences with quantitative experience Exp: 1 year working |
Westat is seeking a research assistant to work on survey research projects, assisting expert data managers in defining and processing survey data and metadata from collection through delivery to Westat’s clients. Data review and documentation writing are both part of the role. Write technical specifications for programming survey instruments and analytic variables. Define data dictionaries for complex files, test survey instruments to ensure accurate data capture, and review collected data at the detailed level. | 3/21/2020 |
| 11917 | Westat Rockville, MD Research Analyst MS in social sciences Exp: 1 year |
Westat is seeking a Research Analyst to work on survey research projects, defining and processing survey data and metadata from collection through delivery to Westat’s clients. Data review, data operations specifications and file documentation writing are part of the role. Write technical specifications for programming survey instruments and analytic variables. Create data descriptions and harmonize data from multiple sources; the data are collected in a variety of technologies and formats with a wide breadth of subject areas. | 3/21/2020 |
| 11918 | Westat Rockville, MD Medical Records Abstractor HS Diploma/GED Exp: 1 year in medical terminology |
The primary role of the medical record abstractor (MRA) is to review medical records in a sampled hospital's emergency department(s), abstract specific information from the patient's chart following the project's case identification protocol, and entering the information into a data collection tool. | 3/21/2020 |
| 11919 | Worldwide Clinical Trials San Antonio, TX PRN Research Technician I HS Diploma/GED Exp: 0-2 years as lab technican |
The PRN Research Technician 1, works under the direct supervision and guidance of the Assistant Supervisor, Laboratory Services, and the Supervisor, Laboratory Services performing technical and laboratory procedures following Worldwide Clinical Trials Clinical (WCT) procedures and study protocol requirements. | 3/21/2020 |
| 11920 | Worldwide Clinical Trials Morrisville, NC Evidence Clinical Research Associate (CRA) BS/BA in medical/health/physical sciences Exp: 0-2 years |
The Clinical Research Associate (CRA), Evidence is responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly registries and other types of non-interventional studies. The CRA, Evidence will typically be involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and negotiating contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the sites activities during study maintenance, and closing down research activities at the sites once the study has concluded. | 3/21/2020 |
| 11921 | Worldwide Clinical Trials Morrisville, NC Clinical Operations Assistant BS/BA in medical/health/physical sciences Exp: 1 year in clinical research |
The Clinical Operations Assistant is a full-time position responsible for completing all assigned projects for Clinical Operations in a timely and accurate manner while interfacing directly with in-house personnel and field employees. Key functions include management of essential document submission to Trial Master Files, supporting field personnel with Microsoft Office, and providing additional administrative support when time permits. | 3/21/2020 |
| 11922 | Wright Medical Kent, WA Hub Material Handler II - Kent, Washington AS/AA Exp: 1-3 years |
This role will ensure the timely processing of kits/sets in the Hub. This could include, but is not limited to, checking in sets, verifying completeness, restocking, creating new kits from sterile implant skus, and other basic set maintenance. The Hub Material Handler II is required to function with minimal supervision to ensure that work flow is uninterrupted and that all customer requirements are met within the functional area. The Hub Material Handler II will be cross-trained on other Hub positions in order to ensure that all Hub functions are carried out timely and as needed. | 3/21/2020 |
| 11923 | Wright Medical Indianapolis, IN Associate Sales Representative, Upper Extremities - Indianapolis, IN BS/BA Exp: 0-2 years |
This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. | 3/21/2020 |
| 11924 | Wright Medical Worthington, OH Hub Material Handler II AS/AA Exp: 1-3 years |
This role will ensure the timely processing of kits/sets in the Hub. This could include, but is not limited to, checking in sets, verifying completeness, restocking, creating new kits from sterile implant skus, and other basic set maintenance. The Hub Material Handler II is required to function with minimal supervision to ensure that work flow is uninterrupted and that all customer requirements are met within the functional area. The Hub Material Handler II will be cross-trained on other Hub positions in order to ensure that all Hub functions are carried out timely and as needed. | 3/21/2020 |
| 11925 | Wright Medical Philadelphia, PA Material Handler I - Philadelphia, PA HS Diploma/GED Exp: 1+ year in delivery |
The Hub Material Handler I is responsible for making pickups and deliveries of implants and instruments to and from local hospitals, surgery centers, clinics/doctor’s offices, the airport, bus station, and other locations for expedited shipments. Excellent communication must be maintained with adaptability to the needs of the customers, sales management/reps, and both corporate and office personnel to ensure timely transportation of goods for surgical procedures. This position has responsibilities to be the liaison between the field office and Wright Medical customers for coordinating activities relating to the efficient use of company assets. | 3/21/2020 |
| 11926 | Wright Medical Dover , DE Associate Sales Representative, Upper Extremities BS/BA in related Exp: 0-2 years in sales |
This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. | 3/21/2020 |
| 11927 | WuXi AppTech St. Paul , MN Associate Chemistry Specialist BS/BA Exp: 0 years |
The Associate Chemistry Specialist will perform a variety of testing preparation techniques, including sample preparations/extractions, reagent preparation procedures and solvent exchange. The position will also include performing a variety of routine benchtop and analytical analysis. Extract test samples using soxhlet, submersion, and fluid path techniques. Perform benchtop testing, including pH, non-volatile residue, USP wet chemistry, and other entry level techniques. | 3/21/2020 |
| 11928 | WuXi AppTech St. Paul , MN Associate Quality Assurance Specialist BS/BA Exp: 0 years |
The Associate Quality Specialist is responsible for ensuring GLP studies, GMP testing, and GMP manufacturing activities are executed in accordance with the appropriate regulatory bodies and internal procedures. Ensures compliance to Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP). Perform job specific tasks in compliance with applicable Regulations, International Standards, and WuXi AppTec Policies and Standard Operating Procedures. | 3/21/2020 |
| 11929 | WuXi AppTech King of Prussia, PA Assocaite Scientist Upstream Process Development BS or MS in relevant field Exp: 0-2 years |
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. Work on defined biopharmaceutical projects for development and/or characterization of vaccine upstream manufacturing cell culture processes. Perform bench scale and pilot scale bioreactor operations in supporting upstream process development, verification, characterization, and tech transfer. Support technical transfer of processes into the non-GMP pilot plant or GMP production facility. | 3/21/2020 |
| 11930 | WuXi AppTech King of Prussia, PA Assocaite Scientist Upstream Process Development BS or MS in relevant field Exp: 0-2 years |
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. Work on defined biopharmaceutical projects for development and/or characterization of vaccine upstream manufacturing cell culture processes. Perform bench scale and pilot scale bioreactor operations in supporting upstream process development, verification, characterization, and tech transfer. | 3/21/2020 |
| 11931 | WuXi AppTech Philadelphia, PA Associate Scientist - Process Development, Downstream MS in biological sciences/engineering Exp: 0-2 years |
Scientist contributing to the development of early and late stage clinical manufacturing processes and commercial manufacturing processes for Cell and Gene Therapies. This position will work with a team of scientists and technical specialists responsible for process development, technology transfer and GMP manufacturing to ensure the application of well-designed unit operations for inclusion in routine manufacturing operations supplying clinical and commercial materials. Responsible for supporting development project leads in the development, scale-up/out, and verification of clinical and commercial manufacturing processes. Contributes to operations of development team, and may support tech transfer activities as necessary. | 3/21/2020 |
| 11932 | WuXi AppTech Philadelphia, PA Associate Raw Material Specialist MS in biological sciences/engineering Exp: 1+ years in GMP manufacturing/QA |
Maintains current knowledge of regulatory guidelines and requirements related to control and testing of raw materials for advanced therapy manufacturing. Authors and revises controlled documents to support material onboarding and risk management. Performs verification of Material Item Masters and works cross-functionally with Supply Chain and Quality Assurance. Creates and maintains end-user resources and tools. Supports delivery of client-specific material risk control and assessment documents as needed. | 3/21/2020 |
| 11933 | Kite Oceanside, CA Manufacturing Associate I BS in biology or related Exp: 0-1+ year(s) |
We are seeking a highly motivated Manufacturing Associate to support our new Viral Vector biotechnology facility in Oceanside, CA. Under minimal supervision, in this role you will be accountable for and focused on front line manufacturing of viral vectors. Responsibilities (include, but are not limited to): Assist with startup activities of a new cGMP facility by collaborating with PD, MSAT, Engineering and Quality departments. Perform all tasks associated with the manufacture of viral vectors following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations. Work as part of a team to execute GMP runs in close collaboration with Process Development and Quality. etc. | 3/18/2020 |
| 11934 | Kite El Segundo, CA QC Microbiology Tech I BS in microbiology Exp: 1+ year(s) |
We are seeking a highly motivated individual to join us as a QC Microbiology Technician in our commercial cell therapy production center located in El Segundo CA. You will work with the Quality Control team in supporting our efforts in this exciting new area of cancer immunotherapy. This position provides Quality Control microbiological testing for clinical and commercial manufactured product, responsible for product testing, utility testing and environmental monitoring. Responsibilities (include but are not limited to): Perform environmental monitoring of cleanrooms. Collect water samples. Perform microbiological assays such as Gram Stain, Endotoxin, Sterility, Microbial Identification, Growth Promotion, Bioburden and Plate Reading. etc. | 3/18/2020 |
| 11935 | Krystal Biotech Pittsburgh, PA Computer Systems Validation (CSV) Analyst unspecified Exp: 1-3 year(s) |
Krystal Biotech, Inc is seeking a highly motivated Computer Systems Validation (CSV) Analyst. This role will have responsibility to support CSV activities of systems and programs requiring system and/or software qualification and testing. This will include the validation of new GxP computer systems used in the QC labs and within Manufacturing production. The analyst will be responsible for the development of validation documentation, including User Requirements Specifications (URS), Functional Requirements Specifications and Test Protocols to ensure that the system is fit for its intended use. etc. | 3/18/2020 |
| 11936 | KVK Tech Newtown, PA Sample Management Associate AS/BS Exp: No experience necessary |
Sample Management Associate provides support to Sample Coordinator and performs administrative tasks in the Sample Management Department. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. JOB RESPONSIBILITIES: Performs duties and training to acquire the skills required for sample and standard handling in support of the laboratory. Handling of samples received in Quality Control Laboratory. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. Quality Control related tasks like receiving, documenting, distributing and reconciliation of all samples received in the laboratory. etc. | 3/18/2020 |
| 11937 | KVK Tech Newtown, PA Analytical Chemist BS/MS Exp: 1-4+ year(s) |
Perform analytical testing of raw materials, in-process materials, stability samples, finished products and product development products using different analytical techniques. JOB RESPONSIBILITIES: Operation, Calibration, Qualification, Preventive maintenance and routine trouble shooting of analytical instruments like UPLC, HPLC, GC, AAS, UV spectrophotometer, Dissolution apparatus, Laser Diffraction Particle Size analyzer, etc. Evaluate existing, develop and validate new analytical methods of drug products and drug substance as per FDA, USP and ICH guidelines by different analytical techniques. Document all performed analysis as per cGMP, USFDA and 21CFR211.194 guidelines. etc. | 3/18/2020 |
| 11938 | LakePharma Worcester, MA Scientist I/II MS in biology or related Exp: 1+ year(s) |
We are rapidly growing and seeking a talented individual to join our Vector Technology Team as a Scientist I/II. The employee will be responsible for executing projects within the laboratory, writing study/research plans, and summarizing data to clients and colleagues via technical reports. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. etc. | 3/18/2020 |
| 11939 | LakePharma Hopkinton, MA QC Analyst 1 BS in a life science Exp: 6-24 month(s) |
LakePharma is the leading US-based biologics contract research, development, and manufacturing organization (CRDMO). The company has developed a range of technologies and capabilities in antibody discovery, protein engineering, cell line development, protein optimization, and GMP manufacturing. With comprehensive technologies, integrated platforms, and five facilities located in key biopharma hubs on both the East and West Coast, LakePharma enables and supports the discovery and development of the biologics of tomorrow. Position Summary: Perform supportive activities for general lab readiness, laboratory equipment qualification and method transfers. etc. | 3/18/2020 |
| 11940 | LakePharma Hayward, CA Scientist II/Senior Scientist I, Antibody Engineering MS in molecular biology, biochemistry, chemical engineering or related Exp: No experience necessary |
We are rapidly growing and seeking a talented individual to join our Antibody Center Department, specialized in antibody engineering. The candidate will be part of the Antibody Engineering Group, responsible for phage library construction and screening, new antibody discovery and affinity maturation, as well as the companion biochemical assays. Essential Duties and Responsibilities: Work on various projects for our clients that involve the discovery of novel antibodies or engineering of existing antibodies to improve their functional activities. etc. | 3/18/2020 |
| 11941 | LakePharma Worcester, MA Lab Assistant/Associate Scientist I AS/BS in biology or related Exp: 0-3 year(s) |
We are rapidly growing and seeking a talented individual(s) to join our Molecular Biology Team as an Associate Scientist. The employee will be responsible for executing projects within the laboratory, writing study/research plans, and summarizing data to clients and colleagues via technical reports. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. etc. | 3/18/2020 |
| 11942 | LakePharma Hopkinton, MA Associate Scientist/Scientist Pharma Assays and Analytics BS/MS in biochemistry or related Exp: 1-5 year(s) |
We are seeking a talented individual to join our team as an Associate Scientist/Scientist, based in our Hopkinton, MA facility, supporting the Pharma Assay and Analytics group in the execution of R&D workflows. Essential Duties and Responsibilities: Validate and Perform Cell-based and Enzyme-based assays and related procedures using manual and automated liquid handling equipment, including but not limited to: Enzyme Activity Analysis. Cell-Based Assays. Viral transduction Workflows (BL1/BL2). etc. | 3/18/2020 |
| 11943 | Lampire Biological Laboratories Everett, PA Small Animal Technician HS diploma/BS in life sciences or related Exp: 1 year |
The primary responsibility of this individual is to maintain the overall health and well-being of the rabbits including cage and facility maintenance. This would include the feeding and watering of rabbits, administering treatments, as well as swapping, cleaning, disinfecting, and sanitizing all animal housing units and animal facilities. Responsibilities Include (but are not limited to): Feeding, watering, and administering treatments, including observing and reporting any signs of disease/illness and help to treat minor cases of such findings. Scraping, chipping, and dusting, animal caging units. etc. | 3/18/2020 |
| 11944 | Lampire Biological Laboratories Coopersburg, PA Laboratory Technician HS diploma/BS Exp: 1-2 year(s) |
To facilitate daily operations at the Coopersburg Laboratory by supporting the whole blood, plasma/serum, anticoagulant, brokered and abattoir departments as necessary. Responsibilities Include (but are not limited to): Prepare formulations and products according to established batch records and work orders. Maintain lot number, batch and equipment logbooks in accordance with established procedures. Perform on-line inspection of components/product and immediately notify supervisor of any problems. etc. | 3/18/2020 |
| 11945 | Lampire Biological Laboratories Everett, PA Purification Technician BS in a scientific field Exp: Not necessary for BS candidates |
This position will be responsible for the purification of antibodies at the Everett facility. Responsibilities Include (but are not limited to): Routine buffer preparation for all processes being performed in the department. Protein A and Protein G purification of Normal igGs and other antibodies. Write and revise Standard Operating Procedures (SOP’s) and Batch Records (BR) as needed. Assist in filing, labeling and finished product good inspection. Operate basic Laboratory and Analytical equipment. etc. | 3/18/2020 |
| 11946 | Latham BioPharm Group Elkridge, MD Associate / Senior Associate / Consultant, Quality Assurance BS in a scientific or engineering field Exp: 1-2 year(s) |
At Latham BioPharm Group, Inc., you will support multiple clients to assure their development phase programs meet or exceed industry cGMP requirements by assisting in the creation and implementing corporate Quality Manuals, Quality Policy’s, SOP’s and training programs. In addition, perform batch record; review, approval and disposition of lots and labels. Manage deviations and CAPA identification to closures. Furthermore, you will provide audit support by assisting in conducting vendor qualification through routine scheduled audits. The ideal candidate must be able to work independently and have excellent interpersonal relationship skills with flexibility to adapt to fast pace environment with changing priorities. etc. | 3/18/2020 |
| 11947 | Leidos Biomedical Research Frederick, MD Research Technician BA/BS in a related field Exp: Not necessary for BS/BA candidates |
We are looking for a Research Technician to join our dynamic, interactive, multidisciplinary research team working on AIDS pathogenesis and development of vaccines for prevention of HIV infection and AIDS, working with non-human primate models. The successful candidate will be able to work in a close team environment, consistently follow detailed protocols and instructions, and keep careful records. Specific duties will include: Processing of potentially infectious blood and tissue specimens from non-human primates. Preparation/formulation of drug compounds. Operation of laboratory equipment. Updating and maintaining detailed sample databases. etc. | 3/18/2020 |
| 11948 | Leidos Biomedical Research Frederick, MD Research Technician BA/BS Exp: No experience necessary |
KEY ROLES/RESPONSIBILITIES: Processing blood and body fluids from HIV-infected patients. Performing complete blood cell counts and blood cell differential counts on a Sysmex XNL 350i hematology instrument. Performing manual blood cell differential counts. Documenting results. Performing basic data analysis. Performing quality control evaluations. Monitoring equipment for optimum performance and basic instrument troubleshooting. etc. | 3/18/2020 |
| 11949 | Leidos Biomedical Research Frederick, MD Glassware Processor HS diploma or equivalent Exp: 1+ year(s) |
The Basic Science Program (BSP) pursues independent, multidisciplinary research programs in basic or applied molecular biology, immunology, retro-virology, cancer biology or human genetics. Research efforts and support are an integral part of the Center for Cancer Research (CCR) at the Frederick National Laboratory for Cancer Research (FNLCR). BSP provides procurement and logistical assistance in support of the research activities of the CCR. Operating as a component of the BSP, the Central Glassware Service performs the daily pick up, washing, sterilizing and delivery of laboratory related items and glassware to research facilities located at the FNLCR. KEY ROLES/RESPONSIBILITIES: Picks up soiled glassware items from laboratories, plastic tanks containing disinfectant. Processes dirty glassware by machine washing, drying and sterilizing in a central kitchen facility. Restocks laboratory glassware cabinets with appropriate quantities of standard laboratory glassware. etc. | 3/18/2020 |
| 11950 | Leidos Biomedical Research Frederick, MD Manufacturing Associate, Fermentation BA/BS Exp: No experience necessary |
KEY ROLES/RESPONSIBILITIES: Complete assigned tasks supporting manufacturing laboratory functions. Maintain bacterial and mammalian cell cultures. Perform microscopic technique/cell counting. Operate advanced buffer/media skid, SU and fixed large scale, chromatographic skid equipment, GMP autoclaves and associated equipment, basic lab equipment operation. Follow Standard Operating Procedures. Complete Batch Production Records under current Good Manufacturing Practices. etc. | 3/18/2020 |
| 11951 | LakePharma Hayward, CA Lab Assistant / Associate Scientist, Process Development & Manufacturing BS in biochemistry, biology, or related Exp: 0-5 years |
We are rapidly growing and seeking a talented individual to join our Process Development & Manufacturing - Cell Line Development Team. The successful candidate will be able to execute hands-on laboratory work in cell culture including planning and executing stable cell line development, shake flask production, and bench scale purifications experiments. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. etc. | 3/18/2020 |
| 11952 | Intersect ENT Menlo Park, CA Technician I, Quality Engineering AS/AA Exp: 1 year |
Support Quality Engineering department on various tasks used to support production and development of medical products used in the treatment for ear, nose and throat disorders. DUTIES AND RESPONSIBILITIES: Work with QE and ME in developing procedures, test methods, qualification protocols, and reports. Perform QA investigation testing on returned product/field complaints, NCMR/CAPA or manufacturing line issues. Assist in performing complaint investigations and return goods evaluation as assigned. Perform QA related data entry and data analysis. Perform responsibilities for NCMR coordinator. Assist QE in providing manufacturing line support including routine observation. etc. | 3/17/2020 |
| 11953 | Invenra Madison, WA Research Associate - Cell Biology BS in a biological science Exp: 1+ year(s) |
Invenra is seeking a highly motivated Research Associate with a strong background in cellular biology. This individual will support the Invenra antibody discovery platform. Aspects of the job entail mammalian cell culture and assays, analytical flow cytometry, ELISAs, and immunofluorescence/luminescence assays. In addition, the position will involve general ordering and stocking of lab supplies as well as upkeep of standard cell biology equipment (i.e. incubators, biosafety cabinets, etc.). The position requires strong communication and organizational skills as well as attention to detail. etc. | 3/17/2020 |
| 11954 | Invicro Doylestown, PA Data Management Associate BS in a life science Exp: 1-2 year(s) |
The Data Management Associate plays an essential role in the establishment and maintenance of database standards, the efficient design of sponsor databases, the integration and reporting of data from multiple sources, and the reporting and analysis of key study data metrics. The incumbent will recommend and drive solutions for efficient database design and data reporting. This role is critical for meeting sponsor study data specification requirements. etc. | 3/17/2020 |
| 11955 | Invitae San Francisco, CA DNA Extraction Technician BS in a clinical laboratory science or related Exp: 1+ year(s) |
We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work at our San Francisco location as well as ability to work overtime and off-schedule days as needed. etc. | 3/17/2020 |
| 11956 | Invitae San Francisco, CA Data Analyst, Lab Operations unspecified Exp: 1+ year(s) |
We are seeking a data analyst to join our team. Responsibilities will include monitoring our product pipeline using custom software tools with the goal of assuring samples move through smoothly. Candidates should have experience with UNIX. They are expected to take initiative to automate tasks and troubleshoot the production process through detail-oriented analysis. An important part of this job is to be able to clearly communicate technical findings to non-technical teammates. | 3/17/2020 |
| 11957 | Invitae Cambridge, MA Bioinformatics Engineer, Algorithm unspecified Exp: 1+ year(s) |
As part of the pipeline engineering team, you will be responsible for maintaining, improving, and adding to our catalog of production bioinformatics pipelines across an expanding set of modern assays. You will be responsible for scaling our pipelines as we work toward our goal of providing low-cost genetic answers to billions of people. You will work and learn among an extraordinary set of peers: bioinformaticians, molecular biologists, and software engineers. Your work will directly improve the quality of our product and positively impact each tested patient. | 3/17/2020 |
| 11958 | Jounce Therapeutics Cambridge, MA Clinical Trial Associate (CTA) BS/BA Exp: 1+ year(s) |
The successful candidate will assist with daily clinical trial execution activities and assist in the coordination of documentation associated with the conduct of investigational clinical studies in accordance with Food and Drug Administration (FDA) Regulations, Good Clinical Practice (GCP), and company standard operating policies and procedures. Responsibilities: Key support role to senior Clinical Operations staff; ensures that delegated components of clinical trials are executed to expected and specified quality standards. Responsible for study laboratory sample management, including tracking and vendor management support. Collect trial information and disseminate it to the internal project team, the CRO, and other stakeholders. Schedule and coordinate study meetings, materials and agendas; recording and disseminating decisions and actions. etc. | 3/17/2020 |
| 11959 | Jubilant Life Sciences Spokane, WA Associate, Regulatory Affairs HS diploma/AS/BS Exp: 1 year |
The Regulatory Affairs Associate/Specialist supports the regulatory compliance programs by coordinating the scheduled activities of state and federal reporting, as well as medical complaint handling, ensuring compliance with US and International regulatory agencies. Essential responsibilities include but are not limited to: Associate: Compliance: Oversees state and federal certification and registration requirements to ensure compliance with reporting obligations. Conducts project research and gathers supportive materials. Conducts document fact checking/comparisons, log updates, and tracking/archiving/filing backup. etc. | 3/17/2020 |
| 11960 | Celgene Seattle, WA Research Associate, Viral Vector Process Analytics BS/MS in molecular biology, biochemistry, bioengineering or related Exp: 1-3 year(s) |
The Research Associate will join an analytical team in the viral vector process development group. The Research Associate will perform assays to quantify and characterize adeno-associated virus vector (AAV) and lentiviral vector. AAV and lentiviral vector deliver the genetic information used to re-engage a patient’s own immune system to cure cancer. These viral vectors are key intermediates in Bristol Meyers Squibb CAR-T and TCR cell therapy drug products. Responsibilities: Perform molecular and cell-based analytical assays, process data, review and report results, and follow established laboratory protocols. Maintain accurate and detailed documentation in laboratory notebook. etc. | 3/17/2020 |
| 11961 | Celgene Bothell, WA Facilities Compliance Associate I BS/BA Exp: 0-2 years |
The Associate will support Facilities compliance by overseeing GxP documentation including creation and revision of Standard Operating Practices (SOPs) and associated Work Instructions (WIN). The Associate will be responsible in performing F&E related deviation investigations and CAPA. DUTIES AND RESPONSIBILITIES: Key Responsibilities: Responsible for adherence to all Operating Procedures, protocols, policies, regulatory requirements, GMP, and safety guidelines. Responsible for maintaining all required records and adherence to established guidelines for quality control procedures, GMP’s, and safety. Participate in the development and revisions to the Facilities & Engineering training program. etc. | 3/17/2020 |
| 11962 | Celgene Seattle, WA Research Associate, Viral Vector Process Development BS in bioengineering, chemical engineering, virology, or related Exp: 0-2 years |
The Research Associate will join our viral vector process development group supporting process development, production and characterization of AAV vectors, which are key intermediates in the generation of multiple T-cell derived drug products. The candidate will support AAV programs and advance our capabilities in vector production. Responsibilities: Hands-on experimental work in the development and optimization of upstream (cell culture and transfection conditions) and downstream (clarification, tangential flow filtration, chromatography) unit operations for viral vector production. Support the process development program for AAV vector manufacturing platforms. etc. | 3/17/2020 |
| 11963 | Celgene Seattle, WA Process Engineer I/Senior Research Associate, Process Science and Technology MS in bioengineering, chemical engineering, or related Exp: 1+ year(s) |
BMS company is seeking enthusiastic, self-driven individuals to join its innovation-focused, multi-disciplinary team focused on advancing new, enabling technologies. This development role will be part of a team of associates, engineers, and scientists that develop next-generation processes and technologies for manufacturing adoptive T-cell therapies. The positions will require experimental design, experimental execution, data analysis, drafting of technical reports, and presentation of results. etc. | 3/17/2020 |
| 11964 | Celgene Seattle, WA Research Associate, Product Sciences BS in immunology or related Exp: 0-2 years |
The Cell Therapy Product Sciences department is seeking a Research Associate to support the development of early stage CAR T and engineered TCR cell products. The Product Sciences Team is responsible for developing and executing mechanism of action and characterization studies to support the development of gene-engineered T cell therapies. The primary focus of the Product Sciences Research Associate role will be to build CAR T cell product and process understanding in support of pipeline projects. Successful candidates will have a strong foundation in immunology and/or human T cell biology and experience with implementation and optimization of a broad range of in vitro cell-based and molecular assays. etc. | 3/17/2020 |
| 11965 | Just-Evotec Biologics Redmond, WA Associate Scientist, Functional Biocharacterization BS in biochemistry, molecular biology, chemical engineering, or related Exp: 0-5 years |
Just is seeking a motivated and creative Associate Scientist who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work with a multidisciplinary team for the analytical and functional biocharacterization of large molecule therapeutics and analysis of process impurities. Experience with ELISA binding assays, DNA extraction, and PCR preferred. Additional experience with cell-based and ligand-receptor binding assays, as well as high-throughput methods and liquid handling robotics beneficial. The successful candidate has strong written and verbal communication skills and is interested in ways to improve technology. etc. | 3/17/2020 |
| 11966 | Just-Evotec Biologics Redmond, WA Associate Scientist, High Throughput Analytical BS in biochemistry, molecular biology, chemical engineering, or related Exp: 0-5 years |
Just is seeking a motivated and creative Associate Scientist, who desires a significant opportunity to improve worldwide access to biotherapeutics. We are looking for a motivated scientist to join a fast-paced, collaborative, and multidisciplinary team. As a member of the High Throughput Analytical group, you will support process development through application of H/UPLC and CE methodologies. Additional experience with other analytical techniques as well liquid handling robotics is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. etc. | 3/17/2020 |
| 11967 | Just-Evotec Biologics Seattle, WA Associate Scientist, Protein Expression BS Exp: 0-5 years |
Just is seeking a motivated and creative researcher who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work as a member of a small but highly experienced and innovative team to develop cell lines for the purpose of manufacturing biologic therapeutics. The successful candidate will have experience with cell culture as well as a strong foundation in cell and molecular biology. Experience in cell line development, cell culture automation, and expression vector design, is a plus. The candidate must possess strong written and verbal communication skills, strong organizational skills, a desire to learn new scientific concepts, and an ability to work directly with scientific staff across multiple disciplines. etc. | 3/17/2020 |
| 11968 | KBI Biopharma Boulder, CO Research Associate I/II Particle Core BS/BA in chemical engineering, chemistry, biochemistry, or related Exp: Not required |
KBI’s Particle Characterization Core is looking for a scientist or engineer to become our next colleague and learn the fine art of particle characterization. Our new associate will have an active role in a dynamic laboratory environment that will include learning cutting-edge analytical techniques, development of data analysis tools, establishing direct relationships with clients, and continuing to build a world-class specialty analytical business. If you are eager to learn and want to jump start a career in pharmaceutical analytics, you might be the person we are looking for! etc. | 3/17/2020 |
| 11969 | KBI Biopharma Durham, NC Manufacturing Associate I-Upstream (Night Shift) (temp to hire) BS/BA Exp: 0+ years |
Responsible for a wide variety of cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Follow SOPs, perform daily tasks in a clean-room, retain records and write reports. May also be responsible for troubleshooting. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP’s and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation. Follow specific techniques and operations while demonstrating an understanding of cGMPs and how they apply to specific responsibilities. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. | 3/17/2020 |
| 11970 | KBI Biopharma Durham, NC Manufacturing Associate I/II-Downstream BS/BA Exp: 0+ years |
Job Summary: Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products at high quality levels. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP's and batch records. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. | 3/17/2020 |
| 11971 | Klus Pharma Cranbury, NJ Research Associate, Antibody Discovery BS in cell biology, immunology, or related Exp: 1+ year(s) |
We are currently seeking a highly motivated individual to join the KLUS Pharma to support therapeutic antibody programs. Key Responsibilities: Have interest in implementing process improvement technologies, exhibit initiative, work independently, be technically proficient in the processes assigned to them, and be flexible in a start-up environment. Responsible for the antibody screening and antibody identification, activities include but not limited to cell culture and cell cryopreservation, cell fusion, hybridoma subcloning/expansion and supernatant harvesting, high throughput screening large panels of antibodies derived from immunizations and hybridoma pools with ELISA and flow cytometry. etc. | 3/17/2020 |
| 11972 | KemPharm Coralville, IA Laboratory Assistant BS in a life science or biotechnology Exp: Not required for BS candidates |
The Laboratory Assistant requires a recent graduate, or student currently pursuing a biotech-related degree, who will utilize basic biological, chemical, physical, and life science laboratory skills to perform the following responsibilities: Reports directly to the Senior Group Leader, Chemistry, and indirectly to the EVP, Research & Development, and supports the entire R&D team. Follows standard operating procedures (SOP) for maintaining laboratory equipment and facilities. Assists in the preparation and/or prepares solutions, reagents, starting materials. Performs routine laboratory tests, chemical reactions, and isolation/purification procedures. Coordinates and/or conducts laboratory equipment maintenance and calibration. Keeps laboratory supplies up-to- date and using Quality Assurance techniques and assists with inventory, ordering, receiving and stocking of laboratory supplies and equipment. etc. | 3/17/2020 |
| 11973 | Perkin Elmer Austin, TX Associate Lab Technologist HS Diploma/GED Exp: 1+ years in lab/research |
Seeking candidate who will work as part of the production team to manufacture Next-Gen Sequencing library kits. Job duties include but are not limited to: Making and testing kit components. Quality Control. Pipetting reagents. Labeling tubes | 3/16/2020 |
| 11974 | Perkin Elmer Upper Providence, PA Research Specialist (Tech) BS/BA in biology Exp: 1-3 years in lab environment |
Perform weekly checks on balances (mix of top loader, analytical, and micro balances) in UP09. Perform daily checks on pH meters in UP09. Preparation of recipe based media, including dissolution, mobile phases, and diluents in accordance with protocols/instructions uploaded into Labware • Data review required; data review is performed by the requestor. | 3/16/2020 |
| 11975 | Perkin Elmer Waltham, MA Associate Inside Sales Representative BS/BA Exp: 0-2 years in telemarketing |
The Associate Inside Sales Representative will act as a lead generation professional working closely with a team of Key Account Sales Specialists, Inside Sales Representatives and the Regional Sales Manager. They will plan and conduct outbound calling and/or email correspondence to targeted prospects and clients, and qualify leads generated by the Marketing team. Position partners closely with the regional sales team to effectively drive business in the region. | 3/16/2020 |
| 11976 | Perkin Elmer San Diego, CA Lab Concierge BS/BA Exp: 1 year in administrative/lab services |
Primary liaison for SAP and Maximo work order requests and tracking initiating work order requests and tracking. Check-in and check-out service providers on-site. Expedite service from OEM and third-party service provides and execute escalation procedures as necessary. Ensure required PM and validation calls are assigned as per SOW. Review, verify, and confirm SAP and Maximo are in sync. | 3/16/2020 |
| 11977 | ViaCyte San Diego, CA R&D Engineer I BS or MS in material, chemical, mechanical, or biomedical engineering Exp: 1 year in med device/research |
As a member of the Combination Product Engineering group, the engineer shall support product development, process development, and manufacturing activities involving the combination product. Under direction from more senior team members, the employee shall utilize R&D methods and engineering techniques to develop processes, generate test systems, and improve manufacturing procedures with respect to the combination product manufacturing line. With guidance, the engineer shall write and execute engineering protocols, document reports, and all elements necessary to launch combination products through design control. | 3/16/2020 |
| 11978 | Viant Grand Rapids, MI Technical Operator 1 - 1st Shift HS Diploma/GED Exp: 1 year in manufacturing |
Under the director of the area Supervisor, responsible for production work according to specifications and established policies, procedures, practices and standards. Assembles components. May be required to operate packaging machine. Performs bar sealing/tray sealing duties | 3/16/2020 |
| 11979 | Viant San Antonio, TX Quality Engineer III MS in engineering Exp: 0-5 years |
The Quality function oversees the development of quality standards and protocols for quality assurance testing models. Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment. Interact with customers and provide support for Engineering, Quality Systems and Process engineering. | 3/16/2020 |
| 11980 | Viant Elkhorn, WI OPERATOR - Entry Level HS Diploma/GED Exp: 1 year in manufacturing |
This position ensures that assigned machines/equipment produce product at or above department standards. Responsible to produce, assemble, inspect and pack all parts as per the work instructions for each assigned task or machine. Maintain all required paperwork and documentation to Good Manufacturing Practice (GMP) and ISO 13485:2016 standards. | 3/16/2020 |
| 11981 | Vigene Biosciences Rockville, MD Upstream Manufacturing Associate – Level II/III BS/BA in sciences or engineering Exp: 1-3 years with upstream biologic production |
The Upstream Manufacturing Associate applies a broad knowledge of biological, bioprocess, and mechanical principles to execute complex operations that result in clinical and commercial stage medicines to dramatically improve the human condition through gene therapy. Perform basic to complex activities in seed train, bioreactor, transfection and recovery operations for both suspension and adherent cultures using SOPs and Batch Production Records. | 3/16/2020 |
| 11982 | Vigene Biosciences Rockville, MD Downstream Manufacturing Associate – Level II/III BS/BA in sciences or engineering Exp: 1-3 years with downstream biologic production |
The Upstream Manufacturing Associate applies a broad knowledge of biological, bioprocess, and mechanical principles to execute complex operations that result in clinical and commercial stage medicines to dramatically improve the human condition through gene therapy. Perform downstream purification activities such as Chromatography, TFF, Ultracentrifugation, and Final Formulation steps. Perform various filter integrity tests throughout the process | 3/16/2020 |
| 11983 | Vigene Biosciences Rockville, MD Fill/Finish Manufacturing Associate – Level II/III BS/BA in sciences or engineering Exp: 1-3 years with biologic production |
Perform basic to complex activities in dispensing of Drug Substance and final fill-finish of Drug Product using SOPs and Batch Production Records. Performing critical downstream activities in preparation of fill finish of Drug Product. Document all activities in Batch Records, Logbooks, Forms, etc. Exercise intellectual curiosity by identifying and escalating events and subtle variances that deviate from normal operation. | 3/16/2020 |
| 11984 | Vigene Biosciences Rockville, MD Research Associate BS/BA in chemical/biomolecular engineering, life sciences, etc. Exp: 0-3 years in R&D |
As a part of the Upstream Process Development Team, the Research Associate is responsible for working with clients in evaluation of upstream processes, sourcing reagents, equipment, and materials for specific projects. Working with clients in evaluation of upstream processes, sourcing reagents, equipment, and materials for specific projects and ensuring proper technology transfer from client. Process demonstration using bench-top bioreactors. | 3/16/2020 |
| 11985 | Viiv Healthcare Rockville, MD Data Science – Future Leaders Program, US – 2020 BS/BA in data/computer sciences/engineering or related Exp: 2020 Graduate |
Our Data Science Future Leaders Graduate Program will challenge and support you to grow professionally and personally. You will receive a generous personal training budget and be supported by a technical mentor. You’ll get to meet senior leaders and network with other graduates. You’ll also improve your technical skills while gaining valuable leadership expertise. It all adds up to a role that’s designed to transform talented graduates into key, senior figures. | 3/16/2020 |
| 11986 | Viracor Eurofins Lee's Summit, MO Laboratory Technician BS/BA in biological/physical/chemical sciences Exp: 1 year in lab |
The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Document remedial action, troubleshooting, quality assurance activities and instrument maintenance | 3/16/2020 |
| 11987 | Viracor Eurofins Lee's Summit, MO Laboratory Specimen Processor I, II or III HS Diploma/GED Exp: 1 year in data entry |
The Laboratory Specimen Processor Associate is primarily responsible for performing duties related to accessioning and data entry with a high degree of proficiency. Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other specimen tracking system. Examine samples for accuracy and other requirements (sample type, volume, etc.) | 3/16/2020 |
| 11988 | Viracor Eurofins Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in biological/physical/chemical sciences Exp: 1 year in lab |
The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. | 3/16/2020 |
| 11989 | Viracor Eurofins Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in biological/physical/chemical sciences Exp: 1 year in lab |
The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures | 3/16/2020 |
| 11990 | Viracor Eurofins Lee's Summit, MO IT Business Analyst I BS/BA in biological/physical/chemical sciences Exp: 1-2 years |
The IT Business Analyst supports the organization by assessing the impact of requested changes, capturing and documenting requirements, and ensuring that those requirements are delivered by IT. In addition, the Business Analyst is responsible for the documentation and execution of test plans for the delivered functionality while supporting the business through the implementation process. Business Analysis is part of the Software Development Life Cycle (SDLC) and the Business Analyst will be involved from initial concept through final implementation, including requirements gathering, design, testing and implementation. | 3/16/2020 |
| 11991 | Viveve Englewood, CO Quality Associate Associates minimum, BS/BA preferred Exp: 1-3 years in medical devices quality |
Responsible for supporting the company’s quality compliance activities as part of the Quality System to ensure that these activities are performed in full compliance with the Company Quality System, FDA, QSR and any other appropriate international quality system requirements. | 3/16/2020 |
| 11992 | Viveve Englewood, CO Regional Sales Representative BS/BA Exp: 1-3 years in B2B sales |
Manage the sales performance of assigned region recurring revenue placement goal. Achieve assigned recurring revenue placements. Provide comprehensive reports on sales activity and other pertinent department activity to assist management in strategic planning. Develop sales techniques for obtaining new business and execute strategies consistent with corporate sales plan. | 3/16/2020 |
| 11993 | Vir Biotechnology San Francisco, CA RESEARCH ASSOCIATE – IMMUNOLOGY/ T CELL BIOLOGY BS or MS Exp: 1-5 years in immunology or infectious disease |
The successful candidate will join Vir’s efforts in discovery research aimed at development of novel therapeutic programs. This person will have significant interactions with both the discovery and clinical development teams. Experience in T cell immunology with a focus on antigen recognition is required. The candidate will also be expected to contribute to the discovery of novel T cell immunomodulators for infectious disease. Experience in human immunology with a focus on T cell assays as well as antibody development is desirable. | 3/16/2020 |
| 11994 | Berry Wehmiller Portland, OR Project Accountant (Design Group) BS/BA in finance/accounting/business admin Exp: 0-3 years |
As part of the Design Group financial team, you will provide project finance support, oversight and analysis focused specifically with supporting the local offices and region. Project finance oversight includes, but is not limited to: Reviewing Project Manager project forecasts and entering the finalized version into EMS, ensuring that project revenues and margins are accurately reflected in the system. Preparing and reviewing client invoices and issuing them accurately & timely according to the client agreement to ensure positive project cash flow. | 3/14/2020 |
| 11995 | Berry Wehmiller Baltimore, MD Electrical Assembler (BW Papersystems - Baltimore) HS Diploma/GED Exp: 0-2 years |
Under direct supervision, perform installation and wiring of electrical components on company produced equipment. Read and interpret basic wiring diagrams, specifications, and work orders to determine materials requirements or assembly instructions. Assemble basic electrical or electronic systems or support structures and install components, units, sub-assemblies, wiring, or assembly casings using rivets, bolts, and soldering equipment. | 3/14/2020 |
| 11996 | Berry Wehmiller Baltimore, MD Mechanical Assembler (BW Papersystems - Baltimore) HS Diploma/GED Exp: 0-2 years in automotive maintenance |
Plan and perform a normal range of operations connected with the assembly and erection of company-produced machines. Responsible for the mechanical assembly of box-making machines comprised of feed, printing, cutter, scorer-slotter sections and related units in accordance with design specifications. Work involves working from complex drawings and a considerable number of component parts that require skill and care to align, fit, and assemble into units and obtain exacting operating performance and appearance. | 3/14/2020 |
| 11997 | Berry Wehmiller Portland, OR Project Engineer (Design Group) BS/BA in chemical engineering Exp: 0-2 years in chemical engineering/mechanical facilities engineering |
Interacting with project team, client, and vendors designing and specifying production line and facility layouts. Working directly with vendors specifying equipment. As-building facilities | 3/14/2020 |
| 11998 | Berry Wehmiller Sacramento, CA Project Engineer (Design Group) BS in mechanical/electrical engineering Exp: 1-5 years in project engineering |
Accountability for all aspects of project execution including line layout engineering, mechanical design, vendor/contractor management, equipment procurement, schedule management, project finances, site management and installation support. Simultaneously organize and successfully execute multiple project responsibilities. Maintaining and growing solid client relationships. | 3/14/2020 |
| 11999 | Berry Wehmiller St. Louis , MO Entry-Level Controls Engineer (Design Group) BS in electrical/computer engineering Exp: Entry Level |
The Controls/Automation Engineer will design, program, and troubleshoot packaging machinery and line control systems. This person will travel to top clients across the country to assist in the design of manufacturing processes, help manage projects, develop facilities, and impact the world by conducting themselves with integrity in pursuit of individual and enterprise goals. Create user applications to monitor and control the production of consumer goods, to satisfy various regulatory agencies, using modern industry standards | 3/14/2020 |
| 12000 | Berry Wehmiller Romeoville, IL Entry-Level Project/Process Engineer (Design Group) BS in mechanical/chemical engineering Exp: Entry Level |
The Project/Process Engineer will be accountable for all aspects of project execution including line layout engineering, mechanical design, vendor/contractor management, equipment procurement, schedule management, project finances, site management and installation support. This person will travel to top clients across the country to assist in the design of manufacturing processes, help manage projects, develop facilities, and impact the world by conducting themselves with integrity in pursuit of individual and enterprise goals. | 3/14/2020 |
| 12001 | Vapotherm Exeter, NH Warehouse Associate I HS Diploma/GED Exp: 1-3 years in warehouse environment |
A Warehouse Associate is responsible for proper receipt, handling, storage, count accuracy, transfer, packaging, and shipment of products in and out of the warehouse. | 3/14/2020 |
| 12002 | Varex Imaging Salt Lake City, UT entry Level Production Operator - Day Shift HS Diploma/GED Exp: 0-1 years |
Assembles/processes product, parts and assemblies using hand tools, customized tooling, and/or semi-automated equipment. Follows written process/assembly documentation. Inspects and tests parts, assemblies and product using precision measuring and testing equipment. Adjusts process within defined ranges based on measured results. | 3/14/2020 |
| 12003 | Varex Imaging Salt Lake City, UT Entry Level Production Operator - Day Shift HS Diploma/GED Exp: 0-1 years |
Assembles/processes product, parts and assemblies using hand tools, customized tooling, and/or semi-automated equipment. Follows written process/assembly documentation. Inspects and tests parts, assemblies and product using precision measuring and testing equipment. Adjusts process within defined ranges based on measured results. | 3/14/2020 |
| 12004 | Varex Imaging Salt Lake City, UT Manufacturing Engineer I BS/BA Exp: No experience necessary |
Develops, implements and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies and final assemblies. Interfaces with design engineering in coordinating the release of new products. Estimates manufacturing cost, determines time standards and makes recommendations for tooling and process requirements of new or existing product lines. Maintains records and reporting systems for coordination of manufacturing operations. | 3/14/2020 |
| 12005 | Varex Imaging Franklin Park, MA Manufacturing Engineer BS/BA Exp: No experience necessary |
Develops, implements and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies and final assemblies. Interfaces with design engineering in coordinating the release of new products. Estimates manufacturing cost, determines time standards and makes recommendations for tooling and process requirements of new or existing product lines. Maintains records and reporting systems for coordination of manufacturing operations. | 3/14/2020 |
| 12006 | Varex Imaging Palo Alto, CA Research Associate, Molecular Biology and Radiobiology BS/BA or MS in life sciences Exp: 0-4 years in research |
The Research Associate, Molecular Biology and Lab Management, is an experienced individual responsible for performing molecular biology assays supporting Varian’s radiobiology and drug-radiotherapy screening investigations and managing laboratory equipment and purchasing for the Global Translational Science team. | 3/14/2020 |
| 12007 | Varex Imaging Palo Alto, CA Research Associate: Molecular Biology MS in biological sciences Exp: 0-2 years |
The Research Associate, Molecular Biology, is responsible for planning and executing experiments in support of Varian’s scientific objectives. Reporting to the Manager of the Global Translational Science Team, the Research Associate, Molecular Biology is responsible for planning and executing experiments related to human and mouse IHC in support of Varian’s scientific objectives. | 3/14/2020 |
| 12008 | Veeva Pleasanton, CA Associate Automation Engineer BS/BA in computer/information sciences Exp: 0 years, recent graduate |
Identify automatable test cases that are most likely to catch issues in SaaS CRM product used by end users around the globe. Refine test cases to make for robust automation, make configuration settings and design automation datasets. Develop software for automation testing in Windows OS, Apple iOS, and web browser environments. Maintain/tune automation suites | 3/14/2020 |
| 12009 | Veeva Toronto, Ca Associate Performance Engineer BS/BA in computer science/engineering/math Exp: 0 years, recent graduate |
The Vault Performance Engineering Team works within the Vault Development Team and participates in all phases of the software development life cycle. Test new features pre-production to make sure they will scale and perform. Collaborate with Vault team members in Product Management, Engineering Management and Quality Assurance to help design and develop performance tests | 3/14/2020 |
| 12010 | Veeva Fort Washington, PA Associate Data Analyst BS/BA in computer science/engineering/math Exp: 0 years, recent graduate |
The Associate Data Analyst will be responsible for all aspects of the data analytics process and will be tasked with helping the Data Operations team innovate with a scalable framework for data collection, extraction, reporting, and analysis. Assist in the building of web scraping systems to crawl, extract, and ingest data using common web scraping tools. Understand how to translate high-level design Proof of Concept ideas into actionable tasks and specifications designed to accomplish the goal | 3/14/2020 |
| 12011 | Veracyte South San Francisco, CA Clinical Lab Scientist BS or MS in biological sciences/technology Exp: 1 year in molecular diagnostic testing |
The Veracyte Clinical Laboratory continues to grow! We are seeking a new Clinical Laboratory Scientist (CLS) to perform cutting-edge diagnostic testing on patient specimens in our collaborative, high-energy work environment. S/he will accurately perform molecular genetic testing, using a variety of molecular biological techniques including expression microarray analysis. | 3/14/2020 |
| 12012 | Vericel Cambridge, MA QC Analyst I BS/BA Exp: 1 year in cGMP lab |
Quality Control (QC) is responsible for incoming inspection of components and raw materials, plus quality testing (e.g. analytical, microbiological) of intermediate, stability and final product samples to demonstrate that all products manufactured meet standards required for cGMP operations. Various techniques (e.g. assay transfers, validation and qualification of new instrumentation) are utilized within the Quality Control Laboratory to ensure cGMP compliance. | 3/14/2020 |
| 12013 | Vericel Cambridge, MA Manufacturing Technician BS/BA Exp: 0-2 years in cGMP lab |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. Perform manufacturing procedures inside an ISO Class 7 clean room in accordance to established SOPs, cGMPs, and safety regulations. Perform aseptic manipulations of cell culture lots and final product assemblies. Document production operations in corresponding batch records and log sheets according to cGMPs and established SOPs. | 3/14/2020 |
| 12014 | Vericel Cambridge, MA Lab Assistant HS Diploma/GED Exp: 0-1 years |
The Research and Development (R&D) group within Vericel supports the continuing development, characterization and validation of manufacturing methods, novel assays, new technology and operational improvements. This group manages technology transfers, clinical manufacturing, training, database development, trending analysis and stability. The R&D team plays an important role in commercial manufacturing troubleshooting, root cause investigation, process optimization and product life cycle management. | 3/14/2020 |
| 12015 | Vericel Cambridge, MA Engineer, Validation I MS in life sciences Exp: 1+ years validation experience |
The Validation department performs equipment, utility, cleaning, sterilization, software, and process validation activities to ensure compliance with company procedures and industry standards in support of Operations and Quality Systems for cell therapies products. The department also functions as the liaison with the Metrology department and performs all equipment ownership and quality assurance review responsibilities associated with site calibration activities. | 3/14/2020 |
| 12016 | Vero Biotech Atlanta, GA Quality Assurance Associate (Biotech) BS/BA in sciences Exp: 1-3 years in FDA/cGMP environment |
Responsible for ensuring that the quality of products being manufactured meet the prescribed quality levels. Performs Quality Assurance activities including review of manufacturing and quality inspection documentation. Monitors the quality system including records and results from processes and procedures to ensure product Quality and compliance. Ensuring manufacturing and quality documentation is accurate, maintained, and reflects GMP, procedural and regulatory requirements. | 3/14/2020 |
| 12017 | VGXI Woodlands, TX Manufacturing Support Technician HS Diploma/GED Exp: 1-3 months |
Responsible for the maintenance, cleaning, and sterilization of manufacturing equipment, manufacturing support equipment, supplies, and production areas. Wash all glassware and plastic supplies in a washer or by hand, as needed. Sterilizes materials as requested to ensure the purity of research and GMP materials. | 3/14/2020 |
| 12018 | VGXI Woodlands, TX Process Technician BS or Associates Exp: 0-3 years |
Responsible for the implementation of cGMP in the pilot plant. Write and review SOPs and production batch records. Implement production processes for the manufacture of plasmid DNA. Conduct cGMP production of plasmid products on an ongoing basis. | 3/14/2020 |
| 12019 | Veeva New York, NY Associate Product Manager - New Products BS/BA in computer science/engineering/math Exp: 1-2 years in project management/technical services |
Own and design product features start to finish, including UX design, user stories, specifications, UAT with QA, and customers conversations to ensure effective design. Author high-quality design specifications within an agile methodology based upon industry and customer requirements. Support release and sprint planning to ensure product enhancements support customers at the right time and the right sequence | 3/14/2020 |
| 12020 | Veeva Columbus, OH Associate, Sales Support BS/BA Exp: 0-2 years in customer service/sales |
We are looking for a Sales Support associate to join our team. You will be a partner to the Sales team and manage the operational steps required to effectively engage, retain and support our existing customers ongoing needs related to their Veeva software subscriptions. Our ideal candidate is a motivated, goal oriented, recent college graduate who is interested in developing sales support and customer service best practices. | 3/14/2020 |
| 12021 | Veeva Indianapolis, IN Associate Software Engineer BS/BA in computer science/engineering/math Exp: 1+ years in client-side or server-side programing |
Drive the implementation and delivery efforts for our cloud-based features and products. Write clean, testable, readable code in a team setting using design patterns and object-oriented principles. Create and enhance rich user experiences. Write quality code with high unit and integration test coverage | 3/14/2020 |
| 12022 | Veeva Columbus, OH Associate Automation Engineer BS/BA in computer/information sciences Exp: 0 years, recent graduate |
Identify automatable test cases that are most likely to catch issues in SaaS CRM product used by end users around the globe. Refine test cases to make for robust automation, make configuration settings and design automation datasets. Develop software for automation testing in Windows OS, Apple iOS, and web browser environments. Maintain/tune automation suites | 3/14/2020 |
| 12023 | InBios Seattle, WA Research Associate II - (Molecular Biology - antibody engineering) MS n molecular biology, biochemistry, or related Exp: Not necessary for MS candidates |
We are seeking a motivated individual with experience in molecular biology techniques to join our molecular biology/antibody engineering team. If you enjoy a busy workday, a mix of computer and bench work, and enjoy working both independently and as part of a friendly and motivated team, then we encourage you to apply for this position. Experience and knowledge needed to be successful in this position: In-depth theoretical understanding of molecular biology and strong molecular biology wet lab technique. Experience with DNA sequencing, PCR amplification and plasmid construction. etc. | 3/10/2020 |
| 12024 | Incube Labs San Jose, CA Mechanical Designer BS in mechanical, manufacturing or related engineering fields Exp: 1-3 year(s) |
The Mechanical Designer is a temporary position for a minimum of three months with possibility of extending to six months if needed. The primary responsibility is to provide design and drafting of tools and equipment and their documentation including ECO submission. This position works closely with Engineering, Quality and Manufacturing teams. Major Duties and Responsibilities: Create 3D models and detail drawings by reverse engineering existing tools and fixtures. Work closely with the Engineering and Manufacturing teams to understand design intent and incorporate Geometric Dimensioning and Tolerancing (GD&T). etc. | 3/10/2020 |
| 12025 | Incyte Wilmington, DE Research Scientist, Cell Line Development MS in molecular or cell biology, chemical engineering, or related Exp: 1-3 year(s) |
Our Global BioPharmaceutical Development Group is looking for a Research Scientist, Cell Line Development. This position develops commercially viable cell lines that are used in the production of therapeutic recombinant proteins such as fusion protein, monoclonal and bispecific antibodies. Key responsibilities: Execute experiments to support Cell Line development, including transfection, routing cell passaging and maintenance, secure freeze. Design and execute high throughput assays to screen mAb or BsAb clones, ensure production, product quality, and genetic stability of cell lines. Operate Ambr 15 Fed-batch study to evaluate pools and clones. Execute studies to ensure production, product quality, and genetic stability of cell lines. Qualify single cell plating and imaging workflow to ensure the monoclonality. assessments meet regulatory expectations. Create and maintain research cell banks. etc. | 3/10/2020 |
| 12026 | Innogenix Amityville, NY Quality Control Chemist MS in chemistry Exp: 1 year |
Perform quality control/development activities. Develop, validate and test analytical methods. Analyze raw materials, in-process and finished product samples using modern QC techniques and advanced analytical equipment. Assist Scientists in developing/implementing quality systems and activities. Perform in-process inspections and document results. Assist Scientists in developing and implementing quality systems and related activities. | 3/10/2020 |
| 12027 | Integer Brooklyn Park, MN Manufacturing Team Member 1-1 HS diploma or equivalent Exp: 0-2 years |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. 1. Adheres to Integer's Values, Behavioral Based Safety process and Integer Associate Quality Policy. 2. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). 3. Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. | 3/10/2020 |
| 12028 | Integer Salem, MA Associate Machine Operator - MCE 2nd Shift HS diploma or equivalent Exp: 0-1 year(s) |
The primary purpose of this job is to operate and monitor machines routinely used in the production of the organization's product. May be involved in the basic set-up, calibration and maintenance of equipment and/or perform finish operations. Key Accountabilities and Responsibilities: 1. Adheres to Integer Values and all safety and quality requirements. 2. Operates machinery used in the manufacture of products with close supervision. 3. May be involved in the basic set-up and/or calibration of equipment. etc. | 3/10/2020 |
| 12029 | Integer Salem, MA Associate Machine Operator - Subassembly Weekend Days HS diploma or equivalent Exp: 0-1 year(s) |
The primary purpose of this job is to operate and monitor machines routinely used in the production of the organization's product. May be involved in the basic set-up, calibration and maintenance of equipment and/or perform finish operations. Key Accountabilities and Responsibilities: 1. Adheres to Integer Values and all safety and quality requirements. 2. Operates machinery used in the manufacture of products with close supervision. 3. May be involved in the basic set-up and/or calibration of equipment. etc. | 3/10/2020 |
| 12030 | Integer Trenton, NJ Assembler Operations 1 - 1st Shift HS diploma or equivalent Exp: 1 year |
Assembler has the general responsibility of assembly and production of components. Position Requirements: Assemble products per assembly process specifications. Conduct product testing under supervision of engineers. Maintain all log books and lot control information per standard operating procedures. Fully trained assembler will have the following: Understanding of the assembly processes. etc. | 3/10/2020 |
| 12031 | Integer Plymouth, MA Associate Prototype Builder AS/AA Exp: 0-3 years |
The primary purpose of this role is to perform assembly and inspection operations over a range of new products and/or processes. Will support non-cyclical work which may include prototypes and pre-production lots in preparation for validation, clinical trials or transfers. Will also support multiple builds within the facility including lab and cleanroom environments. With guidance from Engineering on projects and using work procedures, this role provides support to the Engineering teams to meet various deadlines. May provide support to other team members or provide input to the Engineers on assembly, processes, and build/quality documentation. etc. | 3/10/2020 |
| 12032 | Integer Chaska, MN Manufacturing Team Member - 4th Shift HS diploma or equivalent Exp: 0-2 years |
Key Accountabilities and Responsibilities: Adheres to Integer's Values, Behavioral Based Safety process and Integer Associate Quality Policy. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. Assembles component parts as per print. Utilizes both manual and automatic machine operation. etc. | 3/10/2020 |
| 12033 | Integer Plymouth, MA Manufacturing Team Member 1-1 HS diploma or equivalent Exp: 0-2 years |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Adheres to Integer's Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. etc. | 3/10/2020 |
| 12034 | Integra Hicksville, NY Associate Sales Representative, Extremity Orthopedics Reconstruction BS/BA Exp: 0-2 years |
The Associate Sales Representative will be a responsible for Integra’s Extremity Orthopedic Reconstruction product line and solely responsible for sales of these products within a defined territory. Your primary responsibility will be to support and grow business in order to achieve or exceed sales revenue targets. You will provide case coverage, transport trays, and develop select accounts by building relationships, demonstrating extensive product knowledge and providing exceptional customer service. Your primary call points will be plastic surgeons, podiatric surgeons and orthopedic surgeons. 50% of your time will be spent in the Operating Room. You will work side by side with an experienced Account Manager for approximately 18 months. If performance qualifications are met, then you may be offered a Account Manager for a full territory anywhere in the U.S. etc. | 3/10/2020 |
| 12035 | Integra Cordova, TN Warehouse Tech HS diploma or equivalent Exp: 1-5 year(s) |
Responsibilities: Load and unload incoming and outgoing materials and products. Move materials to and from loading docks, delivery trucks, storage areas, and manufacturing areas. Identify and label materials, and record their locations in the warehouse and on the shelves to maintain inventory. Prepare prep kits for production and make necessary work orders associated with each prep kit. Move these kits to assigned location. Operate trucks, forklifts, cranes, and other equipment to move freight. Perform and report cycle counts weekly. etc. | 3/10/2020 |
| 12036 | Integral Molecular Philadelphia, PA Biotechnology Sales Associate BS in biology, chemistry, or other life science Exp: 1+ years |
We are seeking a Sales Associate to join our University City, Philadelphia-based sales, marketing and business development team. Are you a biologist at heart, but want to explore opportunities outside of typical bench work? Are you a team player who likes to meet new people, build professional relationships, and contribute to the success of a growing biotech company? If you answered “Yes!”, to all the above, then this may be the position for you! Opportunities: Be a key part of the sales, marketing, and business development team of a biotech company. Work with senior management in the planning, strategy, and execution of product development. etc. | 3/10/2020 |
| 12037 | Integral Molecular Philadelphia, PA Laboratory Technician AS/BS in biology, chemistry, medical technology, or related Exp: 6 - 24 months |
We seek an entry level Laboratory Technician to perform vital laboratory tasks to support the continued success of our research teams. The candidate will be part of a lab management team that works in a unified and collaborative manner to ensure the efficient operation of the laboratory. Responsibilities: Coordinate multiple tasks with team members to provide needed supplies. Prepare reagents including buffers, chemicals solutions, complex reaction mixtures and media according to established methods and standard operating procedures (SOP). etc. | 3/10/2020 |
| 12038 | Integral Molecular Philadelphia, PA Research Associate I BS in biology, bioengineering, or related Exp: 1-2 year(s) |
We seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. Responsibilities: Conduct laboratory research and support general R&D efforts for customer-based biomedical research. Projects may involve cell culture, virology, DNA preparation, and liquid-handling automation. Perform cell-based assays (Western blot, ELISA, immunofluorescence, flow cytometry). etc. | 3/10/2020 |
| 12039 | Intellia Therapeutics Cambridge, MA Associate Scientist, RNA Oligonucleotide Chemistry BS/MS in chemistry, biochemistry, or related Exp: 1-4 year(s) |
Intellia Therapeutics is seeking an individual to work closely with the RNA Chemistry Team responsible for synthetic oligonucleotides. This individual will be involved in a complete production process for the identification, implementation & fulfillment of synthesis, purification and reaction scheme analytical characterization and method development of oligonucleotides. RESPONSIBILITIES: Hands-on position in an oligonucleotide chemistry lab inclusive of operating, maintaining & calibrating synthesis platforms and other scientific equipment. Synthetic oligonucleotide method and process development participation. Perform semi-preparative and analytical HPLC and LC-MS quality control processes. Solid decision-making on product path with the ability to work independently and collaboratively while problem-solving. etc. | 3/10/2020 |
| 12040 | Intellia Therapeutics Cambridge, MA Senior Research Associate MS in cell or molecular biology Exp: 0-3 years |
Intellia Therapeutics is developing the CRISPR/Cas9 gene editing technology for therapeutic application both in vivo and ex vivo. This work requires the generation of numerous human lentiviral or mouse retroviral tools for target discovery and target validation. The role of Senior Research Associate/Associate Scientist – Lentivirus Production is primarily responsible for the generation, concentration, titration, and curation of viral particle preparations that are needed to support numerous research efforts. etc. | 3/10/2020 |
| 12041 | Intersect Menlo Park, CA Technician I, Quality Engineering (Swing Shift) AS/AA Exp: 1 year |
Support Quality Engineering department on various tasks used to support production and development of medical products used in the treatment for ear, nose and throat disorders. DUTIES AND RESPONSIBILITIES: Work with QE and ME in developing procedures, test methods, qualification protocols, and reports. Perform QA investigation testing on returned product/field complaints, NCMR/CAPA or manufacturing line issues. Assist in performing complaint investigations and return goods evaluation as assigned. Perform QA related data entry and data analysis. Perform responsibilities for NCMR coordinator. Assist QE in providing manufacturing line support including routine observation of manufacturing activities to ensure compliance with manufacturing process instructions and procedures. etc. | 3/10/2020 |
| 12042 | Immunomedics Morris Plains, NJ Manufacturing Specialist I AS/BS in a science or engineering field Exp: 0-1 year(s) |
This position will be 2nd Shift (4PM-2AM) Monday-Thursday. Responsible for pharmaceutical manufacturing in compliance with current Good Manufacturing Practice (cGMP). Responsibilities: Ensures consistent completion of all the planned manufacturing activities assigned to him/herself. Minimize waste of the resources (worktime, materials, and components). Organize workplace to maximize the throughput and minimize risks of errors. Follow well defined procedures closely, with attention to detail. Practice strong aseptic technique. Document activities accurately and clearly as per GDP. Operate manufacturing equipment according to well defined procedures. Daily monitoring of the process. etc. | 3/10/2020 |
| 12043 | Insmed Bridgewater, NJ Senior Research Associate - Medicinal Chemistry MS in chemistry Exp: 0+ years |
The candidate will work with a multidisciplinary team of scientists focused on the discovery, formulation development, and, characterization of novel drug candidates to treat rare lung diseases. Specifically, the candidate will assist with medicinal chemistry efforts including chemical synthesis, purification, and characterization of small molecule drug targets. Responsibilities: Conduct chemical synthesis, purification, and characterization of small molecule drug targets under the direction of a supervising scientist in Insmed’s research labs. Plan and execute assigned experiments, with increasing independence, in support of project goals. etc. | 3/10/2020 |
| 12044 | Guardant Redwood City, CA Client Services Associate BS/BA Exp: 1+ year(s) |
We are looking for a full-time Client Services Associate (CSA). The CSA is responsible for providing exceptional support to Guardant Health customers, the Guardant Health Clinical Laboratory, Sales Representatives, and our billing partners. Responsibilities: CSA is responsible for receiving and responding to all types of communication: phone, email and web inquiries from customers (physician offices, laboratories, and hospitals), sales representatives and patients. Keeping precise and clear documentation of all phone communications and follow up activities. Adhering to Standard Operating Procedures (SOP’s) pertaining to data entry and data verification requirements. Ability to enter and qualify new customer information into Salesforce.com and LIMS. Contact physicians and other medical personnel to obtain missing information required to complete the order entry process. | 3/9/2020 |
| 12045 | Guardant Redwood City, CA DevOps Engineer BS/MS in computer science or related Exp: 1-3 year(s) |
We are building a unique software stack to manage an ecosystem of microservices, RESTful APIs, and data integrations with internal and external systems to deliver useful and elegant user experiences in the extraordinarily complex oncology diagnostic and therapeutic landscape. We connect patients with clinical trials, help clinicians order our test and receive our clinical reports, and deliver valuable genomic datasets to researchers to help uncover important insights into treatment paradigms and drug discovery. Our technology stack reflects our views of using the best tools for the job, employing Java, Python, Ruby along with Kubernetes, Docker, Mule, MySQL, MongoDB, high-performance computing clusters (HPC), and a variety of AWS services to analyze and disseminate vast volumes of genomic data. | 3/9/2020 |
| 12046 | Guardant Redwood City, CA Scientist I -II , Reagent Development MS in molecular biology, genetics, bioengineering, biochemistry, or related Exp: 1-5 year(s) |
To enable Guardant Health to lead the disruption of cancer treatments through non-invasive cancer screening, the Technology Development Team is seeking a highly motivated Scientist I - II to help develop, test, and improve sample preparation technologies for rare variant studies with next-generation sequencing. At Guardant, we leverage the most advanced technologies and work with leaders in many different fields to create the most impactful and meaningful technologies for cancer management. etc. | 3/9/2020 |
| 12047 | Helmer Scientific Noblesville, IN Assembler Level I 2nd Shift HS diploma or equivalent Exp: 1-3 year(s) |
The Assembler I: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. etc. | 3/9/2020 |
| 12048 | Helmer Scientific Noblesville, IN Assembler I - Clean & Pack HS diploma or equivalent Exp: 1-3 year(s) |
Responsibilities: The Assembler I - Clean & Pack: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. | 3/9/2020 |
| 12049 | Hitachi Chemical Advanced Therapeutics Solutions Allendale, NJ Associate Scientist, MSAT BS in a life science or engineering field Exp: 1+ year(s) |
The Associate Scientist, MSAT performs process and analytical experimental studies as part of a team that is effectively delivering cell therapy services to clients in accordance with defined scope of work, timelines, and budgets. This includes supporting clients in process development, technology transfer and continuous improvement of our client's novel manufacturing processes. Our goal is to support our clients in developing commercially viable cell therapy products, so that they can become accessible to all. etc. | 3/9/2020 |
| 12050 | Homology Medicines Bedford, MA Research Associate - Molecular Analytical Development (6 Month Contract) MS in a biological science Exp: 0-4 years |
Homology Medicines is seeking a Research Associate to aid in operational support for methods to characterize AAV vector products. The individual in this role will be a talented and motivated technician who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. This is a largely laboratory-based position with a focus on providing analytical support for characterizing research-grade vectors. Responsibilities: Plans and executes AAV-specific characterization assays, including vector genome quantification by qPCR and ddPCR, viral capsid quantification by ELISA, protein analysis by SDS-Page gels, endotoxin testing, and additional assays as needed. etc. | 3/9/2020 |
| 12051 | Homology Medicines Bedford, MA Research Associate, Analytical Development BA/BS in a biological science Exp: 0-2+ years |
The role of Analytical Development Research Associate is to aid in developing and refining analytical methods to characterize AAV vector products. The individual in this role will be a highly-skilled, talented and motivated researcher who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. This individual will participate in conducting, optimizing and qualifying molecular and bioanalytical assays such as cell-based infectivity, potency, and immunoassay. We seek candidates with proven ability to work independently after initial training and collaboratively to achieve optimized project plans, with the ultimate goal to deliver products that transform the lives of patients. etc. | 3/9/2020 |
| 12052 | Hovione East Windsor, NJ Process Technician - Drug Product Continuous Manufacturing BS in chemical or other engineering Exp: 1-2 year(s) |
The Process Technician will support the installation and qualification of a GMP continuous tablet manufacturing line, highly automated, with Process Analytical Technology enabled control. This position will also support the development and manufacturing activities for drug product and formulation development projects. Main responsibilities: Work in a GMP environment area, executing chemical and physical operations following approved written instructions and in accordance with cGMPs and EHS regulations. Clean/verify proper cleaning of equipment and production areas according with cGMPs. Adhere to the necessary gowning requirements and in alignment with the various room classifications. Ensure that performed activities are recorded in applicable documentation. etc. | 3/9/2020 |
| 12053 | ICON Raleigh, NC Clinical Research Associate BS in a life science Exp: 1+ year(s) |
ICON is currently hiring Clinical Research Associates with at least 1 year of independent monitoring experience in any therapeutic area! You will be supported with manageable sites & protocols, a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and eligible for the annual performance bonus. Additionally, we have innovative technology and provide excellent training to ensure better outcomes. | 3/9/2020 |
| 12054 | Idexx Worthington, OH Medical Lab Technician - Parasitology - temporary HS diploma/AS/BS Exp: 1+ year(s) |
You will be using automated analyzers, microscopes and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries and diseases in support of veterinarian animal treatment. You will be responsible for setting up and running lab tests, and reading and releasing results according to SOPs (Standard Operating Procedures). You can expect to specialize in one or more of the following areas: Parasitology: Examining samples to identify parasites, utilizing fecal flotation and various microscopic techniques. etc. | 3/9/2020 |
| 12055 | Immatics Houston, TX Research Associate - CMC - PD BS in biology, biochemistry, biotechnology, or related Exp: 1-2 year(s) |
The primary purpose of the Research Associate I position is to perform complex, highly specialized and time sensitive technical cell manipulation and/or perform analytical tests to characterize and assess the functionality of final products. Overall Responsibilities: Perform cell growth and manipulation procedures such as cell enrichment, cell evaluation and sorting, cell culture, cellular product cryopreservation, cell product thaw/wash. Perform accurate calculations to determine cell viability, dilutions and cell concentrations. Responsible for aseptic handling of reagents and products and characterization of cells by molecular assays, flowcytometry and functional assays. etc. | 3/9/2020 |
| 12056 | Immucor Waukesha, WI Laboratory Technician - Filling HS diploma or equivalent Exp: 6-24 months |
We are looking to hire a Filling Laboratory Technician. This role is responsible for performing tasks and functions associated with the filling of production. In addition, you must perform routine upkeep and maintenance of the lab including recording temperatures, cleaning, and disposal of contaminated waste. If you’ve got the necessary skills and experience to excel in this position, we want to hear from you. Apply today! Responsibilities: As the Filling Laboratory Technician, your responsibility will be to accurately complete paperwork with minimal corrections and timely entry of time and materials into ERP when required. etc. | 3/9/2020 |
| 12057 | Immune Technology Corp. New York, NY Untitled Sales Position BS in a life science Exp: 1 year |
Full/part time position, responsible for ensuring customer retention through account management and increasing revenue through marketing activities and generation of sales leads. JOB RESPONSIBILITIES: Establishing and retaining customer relationships primarily through phone, e-mail and personal visit. Delivering requested documents, literature, and information to customers. Organizing and maintaining a database of customers and sales leads. Attending tradeshows, exhibits, and industry functions a few times per year. Prospecting sales leads through exhibits and trade shows. etc. | 3/9/2020 |
| 12058 | Helmer Scientific Noblesville, IN Electromechanical Design Technician I AS/BS in engineering or engineering technology Exp: 1-5 year(s) |
Responsibilities: The Electricromechanical Design Technician: Promotes Helmer values as reflected in personal productivity and quality of work; maintains positive internal/external relationships; seeks & considers diverse perspectives; is committed to individual development and achievement of company goals/objectives. Complies with workplace safety procedures. Assembles and update prototype units for new and existing product including mechanical cabinet, electrical wiring and thermal control system. etc. | 3/9/2020 |
| 12059 | Harpoon Therapeutics South San Francisco, CA Clinical Trial Assistant BS in a biology related field Exp: 1+ year(s) |
We are seeking a highly motivated CTA to be responsible for the coordination of activities (primarily administrative tasks) associated with Clinical Trial startup and maintenance under the direction of, or as delegated by a member of the Clinical Trial team. Responsibilities will range from clinical study coordination to data entry projects and general office work. Key Responsibilities: Maintain and/or accelerate timelines for achieving clinical operational milestones. File, track and maintain study activity. Manage and ensure the paper and electronic Trial Master File (eTMF) meets FDA/ICH/GCP requirements. Coordinate execution of Non-Disclosure and Confidentiality Agreements (NDAs and CDAs) with study sites. etc. | 3/9/2020 |
| 12060 | Harpoon Therapeutics South San Francisco, CA Research Associate, Biology BS/MS in cell biology, biochemistry, or related Exp: 1+ year(s) |
The Research Biology group at Harpoon Therapeutics seeks a Research Associate to join our team. Responsibilities include testing of samples in support of both preclinical development and clinical programs, assay development and optimization, and collection of data in support of regulatory filings. Applicants should be capable of working flexibly and expeditiously in a collaborative, innovative and inspiring environment. The ideal candidate will have experience with mammalian cell culture, stable cell line generation, luciferase assays, flow cytometry, and bioassay automation. Good communication skills, good planning, and an ability to meet deadlines are essential. | 3/9/2020 |
| 12061 | Harpoon Therapeutics South San Francisco, CA Research Associate, New Technologies (Assay Development) BS/MS in biology or related Exp: 1+ year(s) |
We are seeking a highly motivated Research Associate to join the New Technologies group at Harpoon. Our growing team is focused on the development of novel, conditionally active biologic prodrugs. These prodrugs are designed to be preferentially active in the tumor, and thus, enable the safe targeting of previously intractable therapeutic targets. The successful candidate will be expected to design and execute experiments to help develop new biologic prodrug candidates, work collaboratively in a cross-functional environment, and have a strong desire to learn new techniques and the underlying scientific rationale. etc. | 3/9/2020 |
| 12062 | Harpoon Therapeutics South San Francisco, CA Research Associate, New Technologies (Immunology) BS/MS in biology or related Exp: 1+ year(s) |
We are currently seeking a Research Associate to join the New Technologies group at Harpoon. Our growing team is focused on the development of novel, conditionally active biologic prodrugs, including our protease-activated T cell engager platform (ProTriTAC). These prodrugs are designed to be preferentially active in the tumor, and thus, enable the safe targeting of previously intractable therapeutic targets. The successful candidate will be expected to design and execute experiments to help develop new biologic prodrug candidates, work collaboratively in a cross-functional environment, and have a strong desire to learn new techniques and the underlying scientific rationale. | 3/9/2020 |
| 12063 | Jubilant Spokane, WA Validation Associate Associates in sciences Exp: 6-12 months in industry |
The Validation Associate works closely with the Validation Specialist in support of capital, contract, and compliance projects. This position is responsible for executing a variety of validation studies, including performance qualifications and/or requalification’s for terminal and component sterilization work. | 3/8/2020 |
| 12064 | Jubilant Salisbury, MD Manufacturing Process Operator HS Diploma/GED Exp: 1 year in manufacturing |
The Process Operator runs, performs set-ups, maintain safe operations, and cleanings of the production equipment. Operates production machinery and follows the procedures per both company & FDA requirements. Meets the requirements for use of manufacturing equipment and other commonly used equipment per standard operating procedures (SOPs). | 3/8/2020 |
| 12065 | TriLink Biotechnologies San Diego, CA Manufacturing Associate I BS in life sciences Exp: 1-3 years |
This position will produce research and clinical grade components and products within ISO 5 and greater environments. The candidate will participate in the set-up, cleaning, operation, and maintenance of laboratory equipment; perform chemical and enzymatic reactions following asceptic procedures. The candidate must document all actions using GMP Good Documentation Practices. This position requires a candidate that can excel as a leader in the laboratory space. | 3/8/2020 |
| 12066 | Tris Pharma Monmouth Junction, NJ Sales Operation Associate BS/BA Exp: 1 year in office/manfacturing |
The Sales Operations Associate assists the generic sales and marketing efforts by providing analytical and operational support to both internal commercial departments and external clients. Collaborating closely with the President, Generic division, the incumbent supports various and diverse sales operations, analytics, and business development projects and on-going tasks. She/he also works closely with the Sales Operations Representative to contribute to, and support, the building, maintaining and enhancing of client business relationships with assigned customers as well as cross functionally with internal departments and external resources on sales operations issues. | 3/8/2020 |
| 12067 | Tris Pharma Monmouth Junction, NJ Technician/Laboratory Assistant – Product Development HS Diploma/GED Exp: 0-2 years in lab/manufacturing |
The Lab Technician assists the Product Development department by performing routine preformulation and formulation development activities per the given instructions of Scientists. Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws Preparation drug-excipient compatibility studies and other Preformulation studies, as instructed | 3/8/2020 |
| 12068 | Twist Biosciences South San Francisco, CA Research Associate BS or MS in biological/chemical sciences Exp: 1-5 years in research |
We are seeking an outstanding, innovative, and creative Research Associate to join our R&D team to develop world-class Next Generation Sequencing (NGS) Products. This Research Associate will play multiple roles within the R&D group and will work within a small team responsible for development of NGS Products with an emphasis on library preparation and target enrichment applications. | 3/8/2020 |
| 12069 | Twist Biosciences South San Francisco, CA Manufacturing Associate, Gene Production Bachelors/Associates in life sciences Exp: 0-2 years in manufacturing environment |
The Manufacturing Associate, Gene Production will be accountable for following scheduled tasks, operating automated liquid handling devices in a safe and efficient manner, Exhibit detail-oriented documentation skills for updating batch records and logs, cleaning and restocking the lab, and practice good lab bench techniques to ensure high quality and consistent products. Manufacture high quality custom oligo containing products in a high throughput MFG lab according to established SOPs. Daily use of traditional molecular biology processes and techniques especially PCR, DNA quantitation and handling, DNA purification | 3/8/2020 |
| 12070 | Twist Biosciences South San Francisco, CA Manufacturing Associate, Custom Vector Onboarding Bachelors/Associates in life sciences Exp: 0-2 years in manufacturing environment |
The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. Manufacture high quality custom oligo containing products in a high throughput MFG lab according to established SOPs. Operation of robotic laboratory equipment and traditional lab equipment (bioanalyzers, centrifuges, sealers, thermocyclers, spectrometers, HPLCs, Next Gen Sequencing etc.) | 3/8/2020 |
| 12071 | UCB Boston, MA Research Associate - Cell Line Generation BS in biological sciences Exp: 1-3 years in lab |
For our Bedford laboratory, we are seeking a highly-motivated full-time Research Associate to perform a variety of complex technical duties involving mammalian cell engineering for signal transduction and reporter assay development. The successful candidate will be responsible for transgene design, generating a variety of disease relevant cell culture models, designing and executing experiments to test engineered cell lines, analyzing data, and communicating results to UCB colleagues. | 3/8/2020 |
| 12072 | Ultivue Cambridge, MA Biomanufacturing Technician BS in chemical/life sciences Exp: 0-3 years |
This individual will focus on applying his/her technical expertise to perform approved manufacturing and analytical processes to make and test reagents for use in kit products and for company internal use. Make, QC test and deliver on-time, high quality and highly reproducible reagents. Perform incoming QC on purchased antibodies and other raw materials. Working in a team, use established protocols to conjugate antibodies, prepare solutions, and produce nucleic acid reagents | 3/8/2020 |
| 12073 | Ultragenyx Woburn, MA Temporary Research Associate, Analytical Testing BS in biological sciences Exp: 0-2 years in industry |
Working in close collaboration with other Analytical Development team members, the Research Associate will perform analytical methods for AAV samples to support the development of our AAV gene therapy programs. Working with the senior research staff, devise improvements in AAV analytical methods, technology, and documentation. Perform basic AAV analytical methods and documentation for sample management and analysis | 3/8/2020 |
| 12074 | United Therapeutics Research Triangle Park, NC Materials Associate HS Diploma/GED Exp: 1+ years in warehouse/manufacturing environment |
The Materials Associate will be responsible for processing incoming material receipts, control and issuance of materials and preparation of product shipments. This individual will be responsible for performing warehouse activities in accordance with UT policies and procedures. | 3/8/2020 |
| 12075 | United Therapeutics Research Triangle Park, NC Seasonal Support Associate - Clinical Operations (Clinical Oversight) BS/BA Exp: 0-1 years |
Support the Clinical Oversight, Training and Standards team with harmonization of clinical development SOPs, study plans, and processes, as well as deployment and maintenance of clinical systems and training. Provide administrative support related to Clinical Oversight, Training and Standards activities | 3/8/2020 |
| 12076 | United Therapeutics Research Triangle Park, NC Research Associate I/II - Bioscaffolds/Lung Function BS or MS in life sciences/engineering Exp: 1-3 years lab work |
Conduct and assist in product development and research efforts for tissue-based regenerative medicine products for treatment of pulmonary hypertension and other lung diseases. More specifically, support decellularization process development and focus on material and functional characterization of lung scaffold and RegenLung construct. | 3/8/2020 |
| 12077 | United Therapeutics Silver Spring, MD Research Software Engineer I MS in computer science, engineering or math Exp: 0-2 years |
As an important part of this effort in your role as a Research Software Engineer, you will integrate models from multiple scales (organ-level to molecule-level) and guide your team members on how to optimize the efficiency of simulations that further our MedicinesForLife® mission. Work with computational biologists to translate mathematical descriptions of physiological and molecular processes into high-performance computer simulations. Develop and analyze complex integrated systems of differential equations and rule-based models at multiple space and time scales | 3/8/2020 |
| 12078 | United Therapeutics Research Triangle Park, NC Bioprocess Technician - Cell Biology AAS/BA/BS in Biology, Cell and Molecular Biology, or Biomedical Sciences Exp: 1+ year in life sciences |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. Routinely perform large-scale primary lung cell culture in 2D and 3D to support process development activities for a tissue engineered product. Assist with generation and maintenance of all master and working cell banks. Routinely perform bioanalytical assays to phenotypically and functionally characterize cells (such as flow cytometry and plate-based assays) | 3/8/2020 |
| 12079 | UPM Pharmacueticals Bristol, TN Microbiologist BS/BA in microbiology or related Exp: 0-2 years |
Performs routine microbiological testing of raw material, in process, finished product and stability following approved specifications and Standard Operating Procedures (SOPs). This may include but is not limited to antibiotic testing, bioburden/microbial limit testing, antimicrobial effectiveness testing, water testing, environmental monitoring, microbial isolation and identification technique. | 3/8/2020 |
| 12080 | Upsher Smith Maple Grove, MN Associate Chemist I - CAS BS/BA in chemistry Exp: 12 college credits in chemistry |
The Associate Chemist I provides analytical and technical support to new product development and completes analytical testing and various laboratory support functions in a timely manner according to cGMP's. Reads, understands and follows the current USP/NF, laboratory SOPs, analytical methods and study protocols. Documents equipment usages and analytical results in a manner that can be readily followed by reviewers and is consistent with cGMP and in-house SOPs. Performs analytical testing according to established or preliminary methods such as cleaning validation samples, dissolutions, assay, impurities/degradation products, content/blend uniformity, pH, viscosity, titrations, general USP testing, residual solvents and other analytical methods. | 3/8/2020 |
| 12081 | Upsher Smith Maple Grove, MN Corporate Sales Representative I BS/BA in business, science, or communications Exp: 1-3 years |
The Corporate Sales Representative is responsible for the development and management of a designated territory with the goal of maximizing sales while improving patient lives. Patients are central to all USL strategies, and the CSR will be responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other healthcare practitioners and members of the health care community. | 3/8/2020 |
| 12082 | Utah Med Midvale, UT Quality Control Engineer - Midvale, Utah BS Exp: 1 year |
Manages complaint handling system. Schedules and conducts or reviews internal quality audits. Reviews and maintains records of internal audits and internal corrective actions, and participates in MRB. Responsible for Quality Assurance review of R&D and manufacturing projects. Gathers, prepares and presents appropriate Company Quality Assurance-related reports. As assigned: develops defect criteria for use in existing products/raw materials, analyzes/investigates defect causes, inspects/tests products/raw materials to determine compliance, failure mode, etc., and participates in company-wide quality-improvement efforts. | 3/8/2020 |
| 12083 | Vanda Grand Rapids, MI Associate Neuroscience Specialty Sales Representative (Grand Rapids, MI) BS/BA or higher Exp: 0-1 years with internship/part-time experience |
As an Associate Neuroscience Specialty Representative, you will be responsible for: Becoming knowledgeable of disease state, product and competitive market knowledge. Educating Healthcare providers on Vanda's product portfolio. Developing relationships with Healthcare providers in order to understand their needs. | 3/8/2020 |
| 12084 | The Ritedose Corporation Columbia, SC Packaging Specialist 2 year technical degree Exp: 12 months |
The Packaging Specialist is responsible for operating and maintaining the equipment on their respective shift and support of the overall department’s performance goals. They are responsible for the completion of operations on a daily basis. This includes meeting the daily packaging output goals, following the procedures as defined by SOP’s, and executing specific verbal directions from their direct leadership | 3/7/2020 |
| 12085 | West Pharmacuetical Services Exton, PA Associate Packaging Engineer BS/BA in packaging, chemical, mechanical engineering or related Exp: 1-3 years |
Provide project support for the development of new packaging, products, and technologies. Contribute to the selection of materials, create specifications, and manage tasks associated with the development of unique and functional packaging that enhances and preserves the value of West’s products. Perform packaging process development activities and equipment setup as appropriate in laboratory and production environment following all appropriate cGMPs and company policies and procedures. | 3/7/2020 |
| 12086 | West Pharmacuetical Services Tempe, AZ Lab Quality Auditor & Inspector HS Diploma/GED Exp: 1-3 years |
In this role, you will provide total manufacturing quality inspection services including: manufacturing inspection, quality inspection, quality control, sampling inspection, documentation and record keeping. You will also complete and maintain all documentation necessary to ensure conformity to specifications and traceability of records. | 3/7/2020 |
| 12087 | West Pharmacuetical Services Kinston, NC Extruder Operator HS Diploma/GED Exp: 1-3 years cGMP experience |
Ideal candidates are quick thinking and confident to ensure consistent processing and foresight to know the next task required. It is the responsibility of this individual to ensure that product/customer specifications are followed always. Ideal candidates have previous cGMP experience. Duties include: Extrude quality stock of enough quantities required to run our molding presses to produce molded parts that meet our customer’s specifications. Set up Dispersion Enhanced Systems (DES) with a screen pack and Breaker Plate for formulas to be ran while maintaining traceability for all formulations running on the extruder. | 3/7/2020 |
| 12088 | West Pharmacuetical Services Tempe, AZ Mold Technician (Day Shift) HS Diploma/GED Exp: 0-3 years |
Performs labor along a production line. Operates, inspects, and troubleshoots production line machinery and /or assemblies. Ability to work from verbal instructions or from drawings and sketches to plan, construct, alter, assemble, or rebuild a variety of tooling, test fixtures, tools, mold and die components, or related assemblies or equipment. Check work quality continuously, making equipment adjustments and other related changed if necessary, after consulting with Lead person. | 3/7/2020 |
| 12089 | West Pharmacuetical Services Tempe, AZ Operator (Multiple Shifts) HS Diploma/GED Exp: 1-3 years in manufacturing |
West is looking for a motivated operator to join our top-quality production team. In this role, you will perform labor along a production line. Operates, inspects, and troubleshoots production line machinery and /or assemblies. Visually inspects, ensures, and assembles parts in process to quality specifications, being aware of critical visual and dimensional defects and determines acceptability of the parts, based on customer specifications. Assures accuracy of product packaging and tractability as required, including generating labels, the correct labeling of containers, and accurate part count. | 3/7/2020 |
| 12090 | West Pharmacuetical Services Scottsdale, AZ Calibration Technician HS Diploma/GED Exp: 1-3 years in calibration/maintenance |
In this role, you will oversee, coordinate, and execute equipment and facility calibrations in accordance with ISO 13485 requirements. Oversees the maintenance and execution of the calibration program to ensure compliance to standards, including ISO 13485 and FDA 21CFR820. Maintains calibration schedule for facility and equipment – including, but not limited to, logs, records, files, and other documentation for both internal and external calibrations. | 3/7/2020 |
| 12091 | West Pharmacuetical Services Tempe, AZ Associate Manufacturing Engineer BS/BA in engineering or sciences Exp: 0-3 years |
In this role, you will support the manufacture and startup new Plant equipment and equipment upgrades as assigned. Assist with providing engineering support with hands on expertise and practices in projects from conception through production. Interact with engineering, management, site and corporate team members and/or vendors to develop engineering specifications for new equipment or required process improvements; maintain drawings; maintain project timelines; continuously evaluate projects from the tasks, resource and costs perspective, ensure delivery of the projects on time and within budget; and actively install, start-up, and validate equipment or tooling. | 3/7/2020 |
| 12092 | The Weinberg Group Washington, DC Researcher BS/BA in life sciences Exp: 1-2 years |
Is an expert at identifying sources and searching for relevant information. Retrieves, researches, and compiles data to support client projects. Conducts analysis of scientific data and regulatory information. Summarizes regulatory information and pertinent scientific literature for assigned projects. | 3/7/2020 |
| 12093 | TherapeuticsMD Boca Raton, FL Help Desk Technician HS Diploma/GED Exp: 1-2 years in computer related work |
Primary responsibility is to work the queue of Help Desk tickets from users within the company and resolve their requests or escalate to other staff for more complex requests. Respond to and log requests received via the Help Desk system, email, phone, or other avenues. Build/repair PCs and other computer equipment. | 3/7/2020 |
| 12094 | Theravance Biopharma South San Francisco, CA Research Associate I/II, Biology & Pharmacology BS/MS Exp: 1-4 years pharma research experience |
This individual will join a multi-disciplinary team to develop, automate and conduct biochemical and cell-based assays to help drive lead optimization and obtain mechanistic insights for all research programs. Will play a key role in developing, optimizing, and automating new assays. Will conduct compound screening for SAR support and perform quality data analysis. | 3/7/2020 |
| 12095 | ThermoFisher Lexington, MA Associate I, Upstream Manufacturing BS/BA Exp: 1-3 years in cGMP manufacturing |
Responsible for cGMP Upstream manufacturing operations at the Viral Vector Services Thermo Fisher Scientific Lexington, MA. Executing aseptic operations within a biosafety cabinet and cleanroom environment. Performing operations in an aseptic seed lab, operating Wave bioreactors, operating adherent / stir tank bioreactors. | 3/7/2020 |
| 12096 | ThermoFisher Millersburg, PA Material Handler I - Weekend Shift / Nights HS Diploma/GED Exp: 0-2 years related experience |
Pick, pack, sort, arrange, count, store, and correctly process items for storage and/or shipment in accordance with established procedures and customer requirements while sustaining a high level of quality to ensure customers receive correct product and in the time requested. Receive materials and/or finished goods on a daily basis. Verify the quality, type and amount of materials received are correct and that the appropriate documentation is present (e.g. packing list). | 3/7/2020 |
| 12097 | ThermoFisher St. Louis, MO Biopharmaceutical Technician II- Nights HS Diploma/GED, BS/BA preferred Exp: 1-2 years in GMP preferred |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 3/7/2020 |
| 12098 | ThermoFisher Carlsbad, CA Biostatistician MS in statistics/biostatistics Exp: 1-3 years |
As an integral part of the Research and Development Team, you will design and execute research and development activities relating to Thermo Fisher Scientific’s next generation sequencing assays and platform development for both the research use only and in vitro diagnostic markets. | 3/7/2020 |
| 12099 | ThermoFisher Fairport, NY Set-Up Technician - Days, Fairport HS Diploma/GED, Technical degree preferred Exp: 1-3 years setup experience |
Under the direction of the Engineering Manager, with a dotted line to the Shift Supervisor, this position is responsible for installing and removing molds and related auxiliary equipment and components from the molding press as well as preparation of setup for appropriate machines as defined. This individual is also responsible to make necessary adjustments to equipment to ensure quality and quantity of production for the assigned area. | 3/7/2020 |
| 12100 | ThermoFisher Miami, FL Manufacturing Technician I HS Diploma/GED Exp: 0-1 years |
Commitment to Safety, by following site safety procedures and utilizing safety equipment as required for daily tasks. Ability to document Near Miss reports, safety opportunities, accident reports, etc. Uses batch record instructions, job aids, standard operating procedures, and product specifications to execute production activities. Maintains accurate documentation, records and logs in accordance with FDA (Food and Drug Administration), GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization). | 3/7/2020 |
| 12101 | Tolmar Windsor, CO Manufacturing Operator I - Derm; 1st Shift, Monday - Friday HS Diploma/GED Exp: 1 year in GMP manufacturing |
The Manufacturing Operator I performs routine activities related to supporting the dermatology team, while ensuring that products are made with quality for our patients. Perform routine sampling and inspections for product attributes (fill weights, product sealing, labeling) of filled products. Assist in the setup/operation/disassembly and cleaning of production filling equipment. | 3/7/2020 |
| 12102 | Tolmar Fort Collins, CO QA Associate I - Process 2nd shift HS Diploma/GED, Associates preferred Exp: 1-3 years |
The Quality Assurance Associate I is responsible for the inspection, testing, record keeping and overall quality assurance support to manufacturing. Follow procedures to determine status or disposition, and properly document results on records and in lab notebooks.Inspect material, components, and finished product against specified requirements. | 3/7/2020 |
| 12103 | Tolmar Windsor, CO Process Development Engineer I BS in engineering, chemical or mechanical preferred Exp: 1 year in engineering environment |
Assists with the design and implementation of aseptic manufacturing processes, instrumentation and equipment from the laboratory through pilot plant and commercial manufacturing scale-up. Understand and improve process and equipment by working with formulation scientists, other engineers, and manufacturing personnel.Assist other Process Development Engineers as needed to refine batch records, implementing changes when necessary to address manufacturing considerations including processing, manufacturability and scale-up. | 3/7/2020 |
| 12104 | Tolmar Windsor, CO Manufacturing Operator I - Aseptic HS Diploma/GED Exp: 1 or more year in GMP manfacutring |
The Aseptic Operator I performs routine activities related to supporting the injectable team, while ensuring that products are made with quality for our patients. Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of "Right the First Time". Assist in setup and manufacture (bulk, fill, stopper, label, and package) clinical supplies and commercial pharmaceutical products in an aseptic environment in accordance with production batch records. | 3/7/2020 |
| 12105 | Torque Cambridge, MA Associate Scientist, T cell Immunotherapy Characterization BS or MS in biological/engineering sciences Exp: 1-5 years |
The successful candidate will contribute to assay development and process/product characterization efforts supporting the development of our Deep-Primed™ cell therapy platform. This lab-based role will work closely in a cross-functional team of immunologists, analytical chemists, and process engineers to support analytical method development/optimization, product characterization, formulation development, and process development efforts. Primary responsibilities include experimental design and execution, data analysis, documentation, and verbal and written communication of results to the team. | 3/7/2020 |
| 12106 | Toxikon Bedford, MA Histology Research Associate BS/BA in life sciences Exp: 0 years |
Toxikon is currently seeking a full-time Histology Research Associate. Qualified candidates should be a team player, have a willingness to learn, be detail oriented, proficiency with computers and have well-developed time management skills. Trimming of tissues and organs harvested at necropsy. Embedding and processing of tissues. Microtomy Routine H&E staining, other stains as required. Maintain and/or create GLP documentation as necessary, including relative SOPs and histology records, Maintain wet tissue archive. | 3/7/2020 |
| 12107 | Toxikon Bedford, MA Research Associate, Extraction BS in sciences Exp: Entry Level |
The successful candidate will work hand in hand with our study directors, quality assurance and sponsors/clients to ensure all medical device preparation aspects are performed per scientific and regulatory standards. Prior to being tested in clinical trials, medical devices are required by the FDA, EU, Japan, China etc. to perform pre-clinical safety testing referred to as biocompatibility. As most medical devices cannot be directly dosed or applied to the test system, they are extracted using common vehicles and solvents which mimic the conditions found in the human body (blood, muscle, lipids etc.). It is these “extracts” which pull compounds out of the devices, which the body would naturally, and these solutions are dosed as equivalent alternative to the original, whole device. This Medical Device Extraction Research Associate position is responsible for the preparation of the medical devices and creating the required dose solutions (extracts). | 3/7/2020 |
| 12108 | Toxikon Bedford, MA Quality Assurance Associate, Micro BS/BA in life sciences Exp: 1-3 years in testing environment |
In this quality assurance role, the appropriate candidate will be responsible for the implementation, functioning, and monitoring of quality assurance activities. This includes monitoring biological and chemical studies, and creating reports in conformance with GLP practices. Candidates will review GMP, GLP and non-GLP reports for accuracy with reference to protocols, Quality Assurance Standards, Standard Operational Procedures, laboratory precision and accuracy limits, as well as reviewing all protocols for compliance and accuracy. | 3/7/2020 |
| 12109 | Toxikon Bedford, MA Laboratory Assistant, In-Vivo HS Diploma/GED Exp: Entry Level |
Toxikon is seeking an entry level lab assistant to work in the In Vivo Biocompatibility department. The successful candidate will haveinteraction with In Vivo Research Associates, In Vivo Study Directors, Vet Care staff and interface with laboratory management regarding all day-to-day activities of the studies. They will be responsible for providing logistical support for the studies being conducted. As a laboratory assistant, you will be responsible for preparing animals for the studies conducted, including shaving, weighing and identification. | 3/7/2020 |
| 12110 | Toxikon Bedford, MA Laboratory Assistant, Extraction Associates in biotechnology/life sciences Exp: Entry Level |
We are seeking a self-motivated and quality focused individual to join our Extraction team as a Lab Assistant. This position will be responsible for preparing medical devices by extraction using common vehicles and solvents for pre-clinical safety testing. Routine mathematic principles, such as surface area calculations, are required to be able to prepare medical devices and create the required dose solutions. | 3/7/2020 |
| 12111 | Toxikon Bedford, MA Clinical Pathology Laboratory Assistant As or BS in biological/chemical sciences Exp: |
Toxikon is looking for a self-motivated and quality first lab assistant to join our clinical pathology lab. The successful candidate with work hand in hand with our lab staff, study directors, veterinarians and pathologists to process data and samples. This position offers great possibilities for growth as exposure to test methods and sample analysis will occur with experience in the lab. You will be joining a fast growing team and will be selected based on both experience, aptitude and a dynamic personality. Toxikon is looking for a self-motivated and quality first lab assistant to join our clinical pathology lab. The successful candidate with work hand in hand with our lab staff, study directors, veterinarians and pathologists to process data and samples. This position offers great possibilities for growth as exposure to test methods and sample analysis will occur with experience in the lab. You will be joining a fast growing team and will be selected based on both experience, aptitude and a dynamic personality. Toxikon is looking for a self-motivated and quality first lab assistant to join our clinical pathology lab. The successful candidate with work hand in hand with our lab staff, study directors, veterinarians and pathologists to process data and samples. This position offers great possibilities for growth as exposure to test methods and sample analysis will occur with experience in the lab. You will be joining a fast growing team and will be selected based on both experience, aptitude and a dynamic personality. | 3/7/2020 |
| 12112 | ThermoFisher Lexington, MA Associate I, Manufacturing BS/BA in life sciences Exp: 0-3 years |
The Manufacturing Associate 1 is an associate with little to moderate level of technical expertise and experience. An MA1 may independently perform routine operations commensurate with their experience and training. An MA1 participates in the day to day operation of a cGMP compliant Manufacturing facility. Responsibilities include performing basic to moderately complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls. | 3/7/2020 |
| 12113 | Fluidigm South San Francisco, CA Research Associate unspecified Exp: 1-3 year(s) |
Fluidigm is looking for a Research Associate to join our Group. The successful candidate will characterize antibodies for use on Fluidigm’s new Imaging Mass Cytometry platform. Description: Perform antibody-metal tag conjugations for a multitude of antibody/tag combination for use in multiplex assays. Perform verification studies on new metal-conjugated antibody products for use with our Mass Cytometry and Imaging Mass Cytometry (IMC) technology. etc. | 3/4/2020 |
| 12114 | Fluidigm Markham, CA Reagent Manufacturing Associate BS in biology, biochemistry, or other life science Exp: 1-2 year(s) |
Fluidigm is seeking a Reagent Manufacturing Associate. The Reagent Manufacturing Associate is a member of our Proteomics Reagent Operations team. The scientist will be accountable for QC testing of raw materials, in-process materials and finished goods for release. This individual will also be a subject matter expert in the development and testing of new QC procedures. etc. | 3/4/2020 |
| 12115 | Fluke Glenwood, IL Field Support Technician II unspecified Exp: 1-2 year(s) |
Performs calibration and repairs of assigned test and measurement products and equipment: Basic calibrations. Analyzes, troubleshoots, makes repairs, resolves technical problems and performs maintenance service on equipment returned to the service center by customers. Achieves a timely turn-around on all equipment and service. Enters data into Oracle and/or an asset tracking database. etc. | 3/4/2020 |
| 12116 | Fluke Glenwood, IL Laboratory Technician II BS in a life science or comparable Exp: 1-2 year(s) |
We are seeking an individual to join our growing Laboratory operations team. Please read on if you are looking for a start to a long term career. Calibrates radiation detection equipment using ionizing radiation sources/techniques. Assures customer satisfaction and on time delivery of calibrated devices. Able to meet production rates. Reviews generated analytical data before assignment of official calibration certificate. etc. | 3/4/2020 |
| 12117 | Fluke Everett, WA Production Assembler/Operator HS diploma or equivalent Exp: 1-2 year(s) |
Product Assembler/Operators perform wet, dry, mechanical and/or electromechanical processes to produce quality saleable product (components, instruments and/or systems). Position may require extended periods of stationary work in assembly and/or light fabrication. Primary Responsibilities: Prepare, process, wind, clean, install, assemble, rework, calibrate, test, solder and/or inspect product at various stages of assembly from component to final. etc. | 3/4/2020 |
| 12118 | Fresenius Kabi Boston, MA Manufacturing Technician I HS diploma or equivalent Exp: 0-2 years |
Key Accountabilities include: Execution of routine production operations, labeling, quality control, inventory management, continuous improvement, maintenance of clean room equipment, carry out work in a safe manner while notifying management of safety issues and risks, assumes other duties and responsibilities as directed by supervisor. This is a 1st shift position; however, the hours vary each week depending on which task you are assigned for that week. etc. | 3/4/2020 |
| 12119 | Freudenberg Jeffersonville, IN Manufacturing Associate - 1st Shift HS diploma or equivalent Exp: None required |
Your tasks: Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements. | 3/4/2020 |
| 12120 | Freudenberg Jeffersonville, IN Manufacturing Associate - 2nd Shift HS diploma or equivalent Exp: None required |
Your tasks: Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements. | 3/4/2020 |
| 12121 | Freudenberg Jeffersonville, IN Manufacturing Associate - Weekend Shift HS diploma or equivalent Exp: None required |
Your tasks: Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements. | 3/4/2020 |
| 12122 | Freudenberg Jeffersonville, IN Manufacturing Associate - Part Time HS diploma or equivalent Exp: None required |
Your tasks: Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements. | 3/4/2020 |
| 12123 | Frontage Exton, PA Scientist- Bioanalytical Services-ICP-MS MS in analytical chemistry, biochemistry, pharmacology or related Exp: 1+ year(s) |
Scientist / Bioanalytical Services Essential Functions Run sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. Candidates with experience in ICP-MS and/or ICP-MS/MS for bioanalytical or other applications are preferred. Duties: Perform high-volume sample analysis and/or data analysis, data QC, and data interpretation. Maintain schedule of projects and timelines. Coordinate study activities with Principle Investigator to ensure efficiency and quality. Aid in the preparation of study summaries and/or reports. etc. | 3/4/2020 |
| 12124 | Gliknik Baltimore, MD Laboratory Research Associate BS in cell biology, microbiology, immunology, biochemical engineering, or related Exp: Entry level |
Gliknik Inc. is seeking motivated, energetic, individuals with an interest in biopharmaceutical drug discovery to learn and conduct laboratory techniques as a laboratory research associate. This position is an entry-level role at Gliknik, located at the UMB BioPark in Baltimore, MD, which discovers and develops innovative large molecule therapeutics for oncology and autoimmune diseases. etc. | 3/4/2020 |
| 12125 | Grail Menlo Park, CA Clinical Laboratory Associate - Accessioning BS/BA in molecular biology or related Exp: 1 year |
The Clinical Laboratory Associate (CLA) - Accessioning will assist in building and establishing GRAIL’s Clinical Laboratory, performing specimen testing and supporting the daily operations of the Clinical Laboratory. The focus of the CLA - Accessioning will be on the receipt, triage, accession, and centrifugation of patient samples submitted to the CLIA laboratory for testing. You Will: Assist in pre-analytical testing activities including specimen processing, quality control, preparation and aliquoting of reagents. etc. | 3/4/2020 |
| 12126 | Grail Menlo Park, CA Core Services Research Associate 1/2 BS Exp: 1+ year(s) |
GRAIL is seeking Research Associates I/II for the LabOps Core Services team, who will be primarily responsible for ensuring the efficient execution of GRAIL assays in support of Research and Development activities. The ideal candidate is a detail-oriented, dynamic team player with experience in both automated and manual NGS assay execution. The candidate will be expected to partner with many functions of our organization - Automation, Product Development, LIMS, Quality, Supply Chain, Biosample Operations, and Clinical Lab - to ensure the successful completion of R&D projects and general Operational support. etc. | 3/4/2020 |
| 12127 | Grail Menlo Park, CA Quality Control Research Associate 1 BS Exp: 1+ year(s) |
GRAIL is seeking a Research Associate for the LabOps Manufacturing Sciences andTechnology team (MSAT), who will be primarily responsible for materials quality control (QC) and associated tasks. The ideal candidate is a detail-oriented, exceptional team player with hands-on laboratory experience. The candidate will be expected to partner with many functions of our organization - Automation, Product Development, LIMS, Quality, and Clinical Lab - to identify systems limitations, implement process improvements, write documentation, and be instrumental in the implementation and operation of an internal QC system. etc. | 3/4/2020 |
| 12128 | GreenLight Biosciences Research Triangle Park, NC Research Associate – Plant Biology BS in biology Exp: 1-2 year(s) |
GreenLight Biosciences is seeking a highly motivated and collaborative Research Associate to join our Crop Protection team. Greenlight is developing cutting edge RNA technologies that address key challenges in global Crop Protection. In this role you will be integrally involved in the discovery and development of novel biopesticides by developing and executing bioassays for crop pests. The ideal candidate will also have molecular biology skills applicable to RNA interference and gene expression analyses. Strong technical, organizational, and communication skills, as well as the ability to maintain a commitment to excellence and high-quality work in a fast-paced milestone driven company, are essential. etc. | 3/4/2020 |
| 12129 | GreenLight Biosciences Research Triangle Park, NC Research Associate Entomology - Contract BS in entymology Exp: 0-3 year(s) |
GreenLight Biosciences is seeking a highly motivated and collaborative Research Associate to join our Crop Protection team. Greenlight is developing cutting edge RNA technologies that address key challenges in global Crop Protection. In this role you will be integrally involved in the discovery and development of novel biopesticides by developing and executing bioassays for crop pests. The ideal candidate will also have molecular entomology skills applicable to RNA interference and gene expression analyses. Strong technical, organizational, and communication skills, as well as the ability to maintain a commitment to excellence and high-quality work in a fast-paced milestone driven company, are essential. etc. | 3/4/2020 |
| 12130 | Grifols Johnson City, TN Biomedical Technician HS diploma/AS/BS in biology, anatomy, or physiology Exp: 6-12 month(s) |
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. | 3/4/2020 |
| 12131 | Grifols Kingsport, TN Biomedical Technician HS diploma/AS/BS in biology, anatomy, or physiology Exp: 6-12 month(s) |
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. | 3/4/2020 |
| 12132 | Grifols Hattiesburg, MS Biomedical Technician HS diploma/AS/BS in biology, anatomy, or physiology Exp: 6-12 month(s) |
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. | 3/4/2020 |
| 12133 | Grifols Clayton, NC Principal Automation Engineer MS in an engineering, computer, industrial, or automation field Exp: 1 year |
The Validation Automation Engineer II is a junior level professional who is responsible for using technology to improve and streamline a manufacturing process through automation validation. Depending on their specific assignment, this person provides automation validation support for projects or within a specific area. The Validation Automation Engineer II will also integrate into supporting a large scale project. He/she is recognized as proficient in their field such as specific control systems, instrumentation, process, utilities, or qualification testing. He/she meets customer needs in support of business goals. In addition, the incumbent will collaborate with other automation and validation engineers. etc. | 3/4/2020 |
| 12134 | Grifols Bristol, VA Biomedical Technician HS diploma/AS/BS in biology, anatomy, or physiology Exp: 6-12 month(s) |
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. | 3/4/2020 |
| 12135 | Grifols Research Triangle Park, NC Sr. Assoc. Research Scientist I MS in biology, chemistry, or toxicology Exp: 1 year |
The selected candidate provides analytical testing support for process characterization, developmental stability studies, and release of preclinical or clinical batches for internal research projects. The individual selected for this position will conduct testing of non-routine sample types in support of process development, characterization, and/or validation and compile data for the generation of multi-user interactive analytical databases. The analyst may participate in development, implementation and validation of new analytical techniques. etc. | 3/4/2020 |
| 12136 | Grifols Dothan, AL Biomedical Technician HS diploma/AS/BS in biology, anatomy, or physiology Exp: 6-12 month(s) |
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. | 3/4/2020 |
| 12137 | Gritstone Oncology Pleasanton, CA Manufacturing Associate I/II, Upstream BS in biological sciences or related Exp: 1+ year(s) |
The Manufacturing Associate will execute activities associated with cell culture manufacturing in a clean room environment. Processes will be focused on viral vector based cancer vaccine products. This role will also need to assist with aseptic filling and buffer prep processes as well as maintain material inventory in labs. etc. | 3/4/2020 |
| 12138 | Gritstone Oncology Cambridge, MA Research Associate GMP/NGS BS in a scientific or health-related field Exp: 1+ year(s) |
The primary role of the Research Associate is to be responsible for the execution of established nucleic acid extraction and next-generation sequencing (NGS)-based cancer genomics workflows including exome and transcriptome sequencing in a cGMP environment. The ideal candidate will have experience in a regulated environment (CLIA/CAP, cGMP) and will be expected to maintain batch record reports, consumable inventory, equipment maintenance and calibration to maintain quality control and compliance. Individuals with experience as a Clinical Lab Technologist or Molecular Technologist are encouraged to apply. etc. | 3/4/2020 |
| 12139 | Guardant Redwood City, CA Research Associate, Technology Development BS/MS in molecular biology, bioengineering, or biochemistry Exp: 1-3 year(s) |
As a Research Associate supporting product and technology development, you will work with members within the team and interface with multiple functions including process engineering, clinical operations, research operations, and bioinformatics. You will be hands on in the molecular biology lab; designing, implementing, and validating new technologies related to liquid biopsy sequencing assays for the early detection and monitoring of oncology biomarkers. You will be utilizing your analytical skills to undertake root cause analyses and identify solution spaces for continuous improvement. etc. | 3/4/2020 |
| 12140 | Guardant Redwood City, CA Research Associate, LUNAR BS/MS in molecular biology, bioengineering, or biochemistry Exp: 1+ year(s) |
The Lunar Research Team focuses on developing and implementing new technologies to improve early cancer detection. We are seeking a highly motivated Research Associate to be hands on in the lab and assist with the planning, developing and use of new molecular assays. You will handle samples from various sources and work with members within the team as well as interface with multiple teams such as process engineering, Tech Ops, and Bioinformatics. etc. | 3/4/2020 |
| 12141 | Guardant Redwood City, CA Research Associate, Tech Ops (Contract) BS Exp: 1-3 year(s) |
As a Research Associate supporting product and technology development, you will work with members within the team and interface with multiple teams including process engineering, clinical operations, research operations, and bioinformatics. You will be hands on in the lab and be required to use existing assays and/or assay prototypes to generate data in support of new technologies related to liquid biopsy sequencing assays. etc. | 3/4/2020 |
| 12142 | Guardant Redwood City, CA Automation Engineer MS Exp: 1+ year(s) |
In this role, you’ll be part of a team that is responsible for automating and scaling complex workflows and implementing processes for a state of the art sequencing lab. You will wear multiple hats and support the development of all parts of a state of the art robotics facility. Your customers will be licensed clinical operators; your goal is to use software and automation to help them focus on extensive screening. The Process Engineer will be involved in all aspects of assay automation development from concept, requirements definition, and manual assay development to adaptation, optimization, troubleshooting and validation. etc. | 3/4/2020 |
| 12143 | GenapSys Redwood City, CA Machine Learning Engineer/Scientist MS in computer science, mathematics, physics, or engineering Exp: 1-4 year(s) |
Machine learning approaches are at the core of GenapSys' methods for generating high quality DNA sequencing data. As a machine learning engineer, you will join forces in the development of cutting-edge machine learning methods that solve key problems in the DNA sequencing, base calling, and variant calling processes. You will work closely with a cross-functional team of life scientists, bioengineers, and data scientists to identify areas where machine learning can make a difference, to conceptualize and develop biological datasets using cutting edge, high throughput platforms, and to analyze these data sets using the best machine learning methods, applied at scale. | 3/4/2020 |
| 12144 | GenapSys Redwood City, CA Research Associate, Clonal Amplification MS in molecular biology, biochemistry, or related Exp: Not necessary for MS candidates |
We are looking for a Research Associate to join in our clonal amplification team to develop a novel clonal amplification platform for the GenapSys sequencer. You will plan and execute experiments, and analyze data under the guidance of Senior Scientist. You must be motivated, organized and detail-oriented with a strong molecular biology foundation and experience in nucleotide assay development. Responsibilities: Develop a novel clonal amplification platform for Genapsys sequencer. etc. | 3/4/2020 |
| 12145 | GenapSys Redwood City, CA Research Associate, Development MS in molecular biology, biochemistry, or related Exp: 1+ year(s) |
We are looking for a Research Associate, Development who will help to drive the development of reliable high-quality DNA sequencing products. The ideal candidate for this role will have some hands-on experience working in a development environment, including developing and optimizing reagents for R & D, developing QC methods and setting specification that correlate with performance, and carrying out stability studies. Experience with DNA Sequencing technology or similar instrumentation is a plus. If this opportunity sounds exciting, and you have the desire to redefine the current paradigm of DNA sequencing, please apply. etc. | 3/4/2020 |
| 12146 | Fujifilm College Station, TX Associate Scientist – Analytical Method Transfer BS/MS in chemistry, biology, or other laboratory science Exp: 1 year |
Essential Functions: Execute method transfers/qualifications/validations based on regulatory guidelines and industry best practices. Perform assays to evaluate the accuracy, precision, specificity, linearity, robustness, and detection/quantitation limits of analytical methods. Maintain laboratory instrumentation and assist with vendor qualifications. Develop expertise on a subset of analytical methods and participate in method troubleshooting activities. Maintain awareness of project timelines and milestones and openly communicate scheduling challenges. etc. | 3/4/2020 |
| 12147 | Fujifilm College Station, TX Associate Scientist, Bioassay Development Associate Scientist, Bioassay Development Associate Scientist, Bioassay Development BS Exp: 1+ year(s) |
The Bioassay Development group is seeking an energetic Associate Scientist with protein chemistry experience to become an integral member of a high performing development team supporting process and formulation development groups. The successful candidate will primarily perform sample analysis using bioassay based techniques such as qPCR, ELISA or plate-based potency assays for the characterization and testing of recombinant protein pharmaceuticals. etc. | 3/4/2020 |
| 12148 | Fujifilm College Station, TX Associate Scientist – Downstream Process Development MS in chemistry, biology, or other laboratory science Exp: 1 year |
Essential Functions: Assist in the development, optimization, and scale-up of chromatography processes (including affinity, IEX, HIC, etc.) and filtration processes (including UF/DF, depth filtration, and sterile filtration, etc.). Operation of chromatographic systems (GE AKTA, and other Unicorn based equipment). Operation of centrifugation equipment. Operation of filtration equipment. Participate in developing and carrying out experimental protocols. etc. | 3/4/2020 |
| 12149 | Fujifilm College Station, TX Associate Scientist/Scientist I, Analytical Development MS Exp: 1+ year(s) |
The Analytical Development group is seeking an energetic Associate Scientist or Scientist I with protein chemistry experience to become an integral member of a high performing method transfer team supporting protocol based activities including technical transfer of methods from donor labs as well as training of colleagues for internal transfer, and qualification, validation and verification of methods. The successful candidate will primarily execute biochemistry based techniques such as UPLC/HPLC (SEC, IEX, RP, glycan, affinity, etc.), capillary electrophoresis (icIEF, CE-SDS), gel electrophoresis, UV, western blot (SDS-Page), plate based assays and spectrophotometry (SoloVPE) for the characterization and testing of recombinant protein pharmaceuticals. etc. | 3/4/2020 |
| 12150 | Fujifilm College Station, TX Automation Engineer BS in electrical, mechanical, or chemical engineering Exp: 1 year |
Essential Functions: Provide support on a daily basis to process control system, building management systems and data historian systems. Perform system software updates, security updates and upgrades to newer version. Support and enforce the data integrity program. Support and maintenance of computerized systems. OSI Soft PI Historian and reporting system configuration and maintenance. Maintain Functional Specifications, Database Design Specifications and Hardware Design Specifications for automation systems. etc. | 3/4/2020 |
| 12151 | Fujifilm College Station, TX Cell Biology Analyst I BS in biology or related Exp: Not necessary for BS candidates |
Essential Functions: Assist with quality control analytical testing of samples provided to the QC laboratory. Assist with executing test qualification and validation of QC test methods. Writes and revises Standard Operating Procedures (SOPs) and other related Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP) documentation. Manages test samples, reagents and reference standards. etc. | 3/4/2020 |
| 12152 | Fujifilm College Station, TX Drug Product Operations – Technician I AS in biology, chemistry, engineering or related Exp: 0-1 year |
Essential Functions: Responsible for the operation of Vanrx SA25 Vial Filling Isolator. Responsible for assisting in the formulation of the bulk drug product in accordance to procedures. Responsible for visual inspection and labeling of filled bulk drug product vials in accordance to procedures. Assist in writing, reviewing, and/or updating Standard. Operating Procedures (SOPs) and Batch Production Records (BPRs). Document and maintain activity records according to cGMP regulations and ensure junior team members are trained. etc. | 3/4/2020 |
| 12153 | Tecomet Woburn, MA Machine Operator -Entry HS Diploma/GED Exp: 0-2 years machining experience |
Under the direction of the Director, Operations, maintains the Quality system as directed. Majority of tasks performed under the supervision of an experiencedmachinist or the Production Manager. Takes direction to learn basic machine operation, setup and maintenance. Duties and tasks are simple andrepetitive. | 3/1/2020 |
| 12154 | Tecomet Woburn, MA Photo Etch Operator - 1st Shift HS Diploma/GED Exp: Entry Level |
The Photo Etch Operator is responsible for processing metal parts in small batches through various chemical baths and rinsing tanks in compliance with Tecomet standards. Process metal parts in small batches through various chemical baths and rinsing tanks. Process panels through conveyorized etch systems per given instructions. Perform in-process visual inspection of chemically cleaned and stripped panels. | 3/1/2020 |
| 12155 | Tedor Cumberland, RI Production Technician HS Diploma/GED Exp: 1-2 years in production |
The Production Technician position performs all tasks involved in the pharmaceutical process following cGMP’s and SOP’s such as wet granulation, dry granulation, tablet compression, encapsulation, tablet coating, packaging and finished product, put product on stability. The position follows standard work methods and practices safe work habits to ensure production is as efficient and safe as possible. | 3/1/2020 |
| 12156 | Teligent Buena, NJ Clean Room Services Operator – 3rd Shift HS Diploma/GED Exp: 1 year in topical/steril filling/manufacturing |
Cleaning and sanitization of controlled cleanroom environments such as Equipment Preparation rooms, , and all ancillary areas. Additional responsibilities may include cleaning and sanitization of process tanks, mixers, compounding and filling equipment, product formulation processes, terminal product sterilization, finished product inspection, etc. Proactively identify equipment issues and perform root cause analysis, make recommendations and aid in implementation for more complex and non-reoccurring issues. | 3/1/2020 |
| 12157 | Tempus Chicago, IL Reagent Quality Control Technologist BS in med tech, clinical lab sciences, or related sciences Exp: 1 year in molecular lab |
Work within a cutting-edge genomics workflow to provide quality control support in a high-volume next-generation sequencing clinical laboratory. Report significant reagent findings/deviations and system deficiencies to lab management, as appropriate. Document all results and findings in order to satisfy CLIA/CAP/NYS-DOH requirements. | 3/1/2020 |
| 12158 | Tempus Chicago, IL Extraction Technologist BS in med tech, clinical lab sciences, or related sciences Exp: 1 year in molecular lab |
Work in a cutting-edge clinical laboratory to support next-generation sequencing workflow with rapid turnaround times. Utilize state-of-the-art automation and robotics to extract nucleic acids. Track sample progress through the next generation sequencing workflow. Perform basic molecular biology protocols | 3/1/2020 |
| 12159 | Tenaya Therapuetics South San Francisco, CA RA II/SRA I - Quality Control and Analytical Development BS/MS in chemical engineering, biological/chemical sciences Exp: 1-2 years in analytical method development |
We are seeking a motivated Research Associate with experience in viral vector analytical methods for our newly formed Technical Operations Analytical Development/Quality Control Group. In this role, you will perform key molecular biology and cell based assays to support Process Development activities; troubleshoot and optimize particular assays as needed; develop new analytical methods to determine the strength, purity and/or potency of viral vector preparations; perform other tasks such as SOP writing, lab maintenance, supply ordering and write-ups of experiments for potential regulatory submissions. | 3/1/2020 |
| 12160 | Tenaya Therapuetics South San Francisco, CA Research Associate - Analytical Development BS/MS in biological sciences, chemistry, physics Exp: 1 year academic/industrial lab experience |
In this role, you will perform key potency, purity and strength assays to support Process Development activities; troubleshoot and optimize particular assays as needed; assist in the development of new analytical methods to determine the strength, purity and/or potency of viral vector preparations; and perform other tasks such as lab equipment maintenance and supply ordering. | 3/1/2020 |
| 12161 | TeraRecon Fremont, CA Technical Support Specialist BS in computer engineering or related Exp: 12 months in MCSE, CCNA or equivalent |
Provide technical support to customers via phone, email or chat utilizing remote access tools provided by TeraRecon. Actively Monitor customer systems for failures/issues and follow-up on those remotely. Analyze and resolve customer service issues associated with TeraRecon products running on Windows Workstations and Windows Server Operating Systems. | 3/1/2020 |
| 12162 | Tergus Pharma Durham, NC Associate Scientist, IVRT AS or BS in chemistry/biology/pharma sciences Exp: 0 years |
Conducts experiments under limited supervision and maintains excellent notebook documentation in a GMP/GLP laboratory following Good Documentation Practices and ALCOA principles. Performs In Vitro Release Testing (IVRT) for topical formulations such as Gels, Creams, Ointments, Films and Ophthalmic Solutions as per customer needs. Prepares solutions for IVRT and High Performance Liquid Chromatography (HPLC) analysis such as Receiving Media and Mobile Phase. | 3/1/2020 |
| 12163 | Terumo Campbell, CA R&D Technician II AS/AA or BS/BA Exp: 0-3 years |
ob Details: 1. Assemble prototype products per design specifications, drawing and/or engineering direction. 2. Assemble parts by using small instruments with or without a microscope, and through the operations of automated/semi-automated equipment. 3. Troubleshoot and suggest creative solutions to design and process issues. | 3/1/2020 |
| 12164 | Terumo Elkton, MD Quality Engineer I BS/BA in engineering or life sciences Exp: 1-3 years in med devices |
Job Summary: This position is responsible for investigating, planning, and implementing improvements in and/or additions to current products and manufacturing processes that directly affects safety, quality, and productivity with the end result of producing a better quality product more efficiently. Ensure compliance to Terumo’s quality policy, respond to customer complaints, perform audits, develop test methods, and/or write procedures for material characterization. | 3/1/2020 |
| 12165 | Terumo Elkton, MD NPD Engineer I BS/BA or higher in engineering Exp: 0-3 years |
Job Summary: This entry level engineering position is responsible for providing engineering support to Terumo Interventional Systems (TIS) new product development activities as defined in Terumo Medical Corporation (TMC) QA101 Product Development Process & Design Controls under the direction and oversight of senior engineering personnel. Key activities may include: collection of voice of customer (VOC) data; development of concepts for feasibility analysis; development of product specifications; new product design, development, verification and validation; preparation of design control documentation; risk management studies and analyses; process development and prototype fabrication; and support of commercialization activities. | 3/1/2020 |
| 12166 | Terumo Elkton, MD NPD Quality Engineer I BS/BA in engineering or life sciences Exp: 1-3 years in med devices QA |
As part of a project team and with the assistance of the manager, the NPD QE I will be responsible for developing sound Design History File deliverables, including, but not limited to, Quality Plans, Supplier Qualification Strategies/Quality Agreements, Manufacturing Quality Plan, Design Verification protocols and reports, and conducting Design History File Verifications at the end of each design control phase. In addition, the NPD QE I will actively participate in design characterization, risk management activities, and design and process validation. | 3/1/2020 |
| 12167 | Terumo Elkton, MD Facilities Technician I HS Diploma or Associates or Trade School Cert Exp: Entry Level |
This position is an entry level position in the Facilities Engineering department. Associate will be expected to perform maintenance on equipment and plant facilities to ensure functional accuracy and completeness, under the guidance and direction of Senior / Lead Facilities Engineers. | 3/1/2020 |
| 12168 | Terumo Somerset, NJ Clinical Research Associate (CRA) BS/BA in life sciences Exp: 1-3 years in monitoring |
Job Summary: PURPOSE: Ensure clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements by engaging with assigned sites. JOB DETAILS: • Perform site selection, start-up/regulatory, initiation, monitoring and close out visits in accordance with contracted scope of work, using good clinical practices, applicable regulations, SOPs and work instructions. • Complete appropriate therapeutic, protocol and clinical research training to perform job duties. • Administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues. | 3/1/2020 |
| 12169 | Teva Tacoma, WA Neuro / Psychiatry Sales Representative - Tacoma, WA BS/BA in related field Exp: 1 or more in business to business sales |
Teva is searching for an experienced Neuro / Psych Sales Representative to join our team in the Tacoma, WA area! As a Sales Representative you will establish and maintain professional relationships with targeted physician groups to maximize new business opportunities. Build rapport and relationships by interacting effectively with employees and external contacts (i.e. HCP and office staff) at all levels, demonstrating the awareness of their needs and responding with the appropriate action. Provide healthcare product demonstrations, physician detailing and in-servicing of products to current and potential customers. | 3/1/2020 |
| 12170 | Teva Rome, GA Neuro / Psychiatry Sales Representative - Tacoma, WA BS/BA in related field Exp: 1 or more in business to business sales |
Teva is searching for an experienced Neuro / Psych Sales Representative to join our team in the Tacoma, WA area! As a Sales Representative you will establish and maintain professional relationships with targeted physician groups to maximize new business opportunities. Build rapport and relationships by interacting effectively with employees and external contacts (i.e. HCP and office staff) at all levels, demonstrating the awareness of their needs and responding with the appropriate action. Provide healthcare product demonstrations, physician detailing and in-servicing of products to current and potential customers. | 3/1/2020 |
| 12171 | Teva Toledo, OH Neuro / Psychiatry Sales Representative - Tacoma, WA BS/BA in related field Exp: 1 or more in business to business sales |
Teva is searching for an experienced Neuro / Psych Sales Representative to join our team in the Tacoma, WA area! As a Sales Representative you will establish and maintain professional relationships with targeted physician groups to maximize new business opportunities. Build rapport and relationships by interacting effectively with employees and external contacts (i.e. HCP and office staff) at all levels, demonstrating the awareness of their needs and responding with the appropriate action. Provide healthcare product demonstrations, physician detailing and in-servicing of products to current and potential customers. | 3/1/2020 |
| 12172 | Teva Olive Branch, MS Warehouse Operator HS Diploma/GED Exp: 1 year in warehouse work |
As a Warehouse Operator I, you will have the opportunity be a part of a growing team dedicated to serving our customers-in-need by driving day-to-day Anda warehouse operations. You will be responsible the picking, packing and shipping of products to our customers in a manner that meets company standards. Additionally, you utilize RF scanning equipment to ensure accuracy in movements. | 3/1/2020 |
| 12173 | Teva Shreveport, LO Sales Represnetitive I BS/BA in related field Exp: 1 or more in business to business sales |
Teva is searching for an experienced Neuro / Psych Sales Representative to join our team in the Tacoma, WA area! As a Sales Representative you will establish and maintain professional relationships with targeted physician groups to maximize new business opportunities. Build rapport and relationships by interacting effectively with employees and external contacts (i.e. HCP and office staff) at all levels, demonstrating the awareness of their needs and responding with the appropriate action. Provide healthcare product demonstrations, physician detailing and in-servicing of products to current and potential customers. | 3/1/2020 |
| 12174 | Teva Salt Lake City, UT Compliance Specialist I BS/BA in sciences/engineering Exp: 0-3 years |
This position will be responsible for vendor management, supporting annual product reviews (APRs)/product quality reviews (PQRs), and providing audit support for Regulatory Agency Inspections, Teva Global Regulatory Audits (GRA), internal audits and Partner audits. The candidate will support and perform tasks related to key compliance processes, including but not limited to, document changes, investigations, CAPAs, change control, metrics, quality agreements, notifications to management (NTMs), FAR submissions, market renewals/submissions, and other related activities. This position will also interact with Partners on occasion under the direction of the department manager. | 3/1/2020 |
| 12175 | Teva North Wales, PA Material Handler I - 1st Shift HS Diploma/GED Exp: 6 months in industrial environment |
Utilizes radio frequency (RF) system and operates fork-lift to receive and put-away inbound (IB) receipts - includes physically breaking down and creating optimal sized pallets prior to put-away into inventory. Utilizes RF system and operates fork-lift to move inventory throughout the warehouse for the purpose of managing inventory and replenishing picking locations. Performs tote picks via tote management system (Pick-to-light module) - includes deployment of totes on PTL module, using PTL module to accurately pick orders from shelf to tote | 3/1/2020 |
| 12176 | TRC Columbia, SC Packaging Specialist HS Diploma/GED Exp: 12 months experience |
The Packaging Specialist is responsible for operating and maintaining the equipment on their respective shift and support of the overall department’s performance goals. They are responsible for the completion of operations on a daily basis. This includes meeting the daily packaging output goals, following the procedures as defined by SOP’s, and executing specific verbal directions from their direct leadership. The Packaging Specialist is responsible for maintaining and ensuring their training is complete. Each Specialist is hired into a minimum level that they are required to attain. | 3/1/2020 |
| 12177 | Tempus Chicago, IL Cell Culture Research Associate (11 am – 7 pm) MS in lab or biological sciences Exp: 0-2 years |
Responsibilities include: Receive and process patient tumor samples for our patient-specific biological modeling. Plate cells to grow tumor organoids and maintain cell cultures. Plate tumor organoids for assays. Cryopreserve tumor tissue and tumor organoids to create the most comprehensive organoid biobank | 3/1/2020 |
| 12178 | Teligent Buena, NJ Compounder I – 1st Shift AS/AA Exp: 1 year in pharma |
Perform functions relating to the processing of Topical products (creams, ointments, lotions, solutions) ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements, and in conjunction with all Standard Operating Procedures (SOPs). Perform functions relating to the cleaning and sanitization of compounding process equipment and compounding facility to facilitate GMP compliance, quality, safety, and schedule attainment. Follow standard operating procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. | 3/1/2020 |
| 12179 | Syros Cambridge, MA Research Associate/Senior Research Associate, Medicinal Chemistry BS or MS in life sciences Exp: 1 year in small molecule drug discovery |
Syros Pharmaceuticals is seeking an experienced, motivated, and energetic Medicinal Chemist to join the discovery research group. Assist in development chemistry plans, strategy, and tactics to efficiently deliver high quality drug development candidates (DCs). Contribute to the design, synthesis, and characterization of novel molecules targeting diverse protein targets. Carry out integrated analysis and interpretation of multi-faceted biological data (activity, selectivity, kinetics, DMPK, physical properties, etc.). | 2/29/2020 |
| 12180 | Syros Cambridge, MA Research Associate I/II, Molecular and Cellular Biology BS or MS in life sciences Exp: 1-2 years |
This lab-based position will focus on performing high throughput screening assays to support drug discovery for oncology projects. The successful candidate will genetically and chemically interrogate cellular systems, perform and eventually develop cell-based screening assays to support discovery and development of small molecule oncology drug candidates. This individual will have the opportunity to learn and master various cutting-edge techniques including FACS, high-content imaging, Meso Scale Discovery (MSD) etc. to support programs as they progress and should be an enthusiastic learner with the ability to pick up things quickly without repeated training. | 2/29/2020 |
| 12181 | System Bioscience Palo Alto, CA Customer & Technical Support Representative (CSR/TSR) BS in life sciences Exp: 1-2 years in life sciences |
The ideal candidate will have a B.S. degree in the life sciences and will support an existing group of customer support personnel taking telephone orders from customers, logging into a CRM system, printing packing slips, sales orders, and shipping documentation, and assist with packaging of life science reagents for shipment to worldwide customers. This position will also provide support to the Commercial Team. | 2/29/2020 |
| 12182 | t2 Biosystems Lexington, MA Software Quality Engineer - Contract BS in computer sciences/engineering Exp: 1-3 years in device testing |
We are seeking an experienced software quality engineer who is excited about the work we do at T2 and will work as part of our Engineering team to verify, validate and release software updates, in compliance with our Quality System. This position reports to the Director of Software Engineering and is based in Lexington, MA. The ideal candidate will have strong organizational and communication skills (verbal and written), a meticulous, detail-oriented work approach and be comfortable following a regulated, formal development and release process. | 2/29/2020 |
| 12183 | Tactiva Therapeutics Buffalo, NY Senior Lab Technician MS in life sciences Exp: 18 months in research lab |
The senior laboratory technician designs and optimizes assay processes including sample preparation, workflow automation, and analytic detection, as well as provides data for critical review of test development. The senior laboratory technician provides direct scientific and analytic support to the laboratory director(s) and monitors timelines to meet production goals and objectives. | 2/29/2020 |
| 12184 | Takeda Greenwood, IN Entry Level Medical Screener / Phlebotomist (Full Time) HS Diploma/GED Exp: Entry Level |
You’ll use your attention to detail to screen new and repeat donors and take and record donor vital signs and finger stick results. You will use our Donor Information System, prepare donor charts, maintain accurate records, and coordinate donor compensation. You’ll work in our fast-paced, team environment; ensure a clean and professional work environment; attend team meetings; work closely with your management team; and problem-solve together. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. | 2/29/2020 |
| 12185 | Takeda Lexington, MA Manufacturing Technician I HS Diploma/GED minimum Exp: 0-2 years in industry |
With direct supervision this individual will perform routine manufacturing operations for the production of clinical and/or commercial products. Operates production equipment according to SOPs in their assigned areas. The individual will carry out cGMP manufacturing cleaning and disinfection operations utilizing Standard Operating Procedures (SOPs). Primary responsibilities. | 2/29/2020 |
| 12186 | Takeda Round Lake, IL Production Associate AS/AA or HS Diploma/GED Exp: 0-2 years in manufacturing |
The Production Associate (PA) is responsible for executing all processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, responsible for the hands-on execution of all activities in the production area | 2/29/2020 |
| 12187 | Takeda Social Circle, GA Manufacturing Technician I AA or equivalent, or BS/BA Exp: BS/BA: 0 years, AS/AA: 1 year |
Executing processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Clean, Set up, operate, and teardown of equipment such as tanks, filtration systems, and production lines. Operate general production equipment (such as pH and conductivity meters, autoclave, portable mixers, etc.). | 2/29/2020 |
| 12188 | Talis Menlo Park, CA Research Associate MS in life sciences Exp: 0-5 years |
The candidate will join the Assay Development group in the R&D division where focus is on molecular assays development such as nucleic acid isolation, purification, amplification and labeling technologies. Work with senior scientists and run hands-on experiments for microbiology, sample preparation, nucleic acid extraction and amplification. Perform detailed data analysis of experiments using Minitab or similar tools and develop summaries for the Assay Development group. | 2/29/2020 |
| 12189 | Tango Cambridge, MA Associate Scientist, Immunology BS or MS in immunology or related Exp: 0-8 years in industry |
We are seeking an innovative, collaborative and enthusiastic immunologist to work on building our Immunology and Immuno-Oncology Programs. This individual will work primarily at the bench to help drive target identification, validation, and patient selection strategies. Culture and engineer primary human T cells, murine T cells, and tumor cells using genetic tools. Assessment of T cell phenotype and function by multicolor flow cytometry, ELISA and gene expression analysis | 2/29/2020 |
| 12190 | Tanvex San Diego, CA Research Associate, Analytical Sciences - #1214 BS or MS in biological/chemical engineering or sciences Exp: 0-3 years |
The Research Associate will perform analytical tests using HPLC, Spectrophotometry (RP, IEX, SEC, HILIC etc.), CE, mass with high quality and efficiency; provides analytical support in R&D settings for samples from various process scales; writes experiment summaries and development reports; and assists during document review comprising of but not limited to: batch records, standard operating procedures and assay protocols. | 2/29/2020 |
| 12191 | Tanvex San Diego, CA Research Associate, Analytical Sciences - #1189 BS or MS in biological/chemical engineering or sciences Exp: 0-3 years |
The Research Associate will perform analytical tests using HPLC, Spectrophotometry (RP, IEX, SEC, HILIC etc.), CE, mass with high quality and | 2/29/2020 |
| 12192 | Target Health LLC New York, NY Biostatistician MS in statistics/bio statistics Exp: 1-3 years is a plus |
Provide statistical support for study design, data transfer, analysis, verification, interpretation of results in clinical trials. Program datasets used for analysis according to CDISC standard, along with data define documentation and data reviewer’s guide. Create and verify listings/tables/figures based on data collected in clinical trials. Work closely with data management, clinical and regulatory departments. | 2/29/2020 |
| 12193 | TCR Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Analytical Process Development BS in biological/chemical sciences Exp: 1-2 years |
This position will require execution of cell culture experiments, assisting the team in analysis of in-process samples, and support of the technology transfer to CMOs. The position represents an excellent opportunity for career development, working closely with experienced scientists, in a fast-paced and highly collaborative environment. Learn and execute on all assays used by the analytical team (qPCR, ELISA, T-cell based assays). Assist in the analysis and characterization of lentiviral vectors for use by multiple internal research groups. | 2/29/2020 |
| 12194 | TE Connectivity Middleton, PA Software Systems Engineer I BS or higher in computer science/engineering Exp: 0-2 years |
TE Connectivity’s Software Systems Engineering Teams provide functional and empirical analysis related to the design, development, and implementation of software operating/automation systems, including, but not limited to, utility, development, and diagnostic software. They perform technical planning, system integration, verification and validation, cost, risk, supportability and effectiveness analyses for total systems. | 2/29/2020 |
| 12195 | TE Connectivity Bellville, TX PRODUCT ENGINEER I BS/BA in mechanical/electrical engineering Exp: 0-2 years |
Actively lead & contribute to New Product Development activities. Provide Sustaining Engineering support for existing product lines. Exercises considerable latitude in determining objectives and approaches to assignment. Drives results primarily through collaboration and influence, not through direct reporting relationships | 2/29/2020 |
| 12196 | TE Connectivity Maple Plain, MN Extrusion Technician HS Diploma/GED Exp: 1-2 years a extruder operator |
General setup, operation and maintenance of PTFE extrusion equipment and tooling to support manufacturing and development efforts in a clean room environment. Facility cleaning, shipping & receiving, QA support as needed, Customer Service support as needed. Overall a multi-functional individual that will wear several hats during our growth needs. | 2/29/2020 |
| 12197 | Synthego Redwood City, CA Research Associate MS in life sciences Exp: 0-2 years |
The Research Associate will pair their scientific skill sets with laboratory and process intuition to figure out new and better ways of performing our work. Our team runs large, automated research campaigns for key customers and internal clients. We are building a new business function at Synthego and you can be a part of it. | 2/29/2020 |
| 12198 | Synthego Redwood City, CA Shipping Associate, CRISPRevolution HS Diploma/GED Exp: 1 year in shipping |
Synthego is looking for a shipping associate to execute our daily order fulfillment activities, ensuring quality and customer satisfaction are top priorities. Coordinate with manufacturing and commercial operations to ensure daily orders are picked, packed, and shipped on-time. Inspect finished product for defects and verify accuracy of order contents and documentation prior to packaging and shipment | 2/29/2020 |
| 12199 | Takeda Round Lake, IL Production Associate AS/AA or HS Diploma/GED Exp: 0-2 years in manufacturing |
The Production Associate (PA) is responsible for executing all processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, responsible for the hands-on execution of all activities in the production area | 2/29/2020 |
| 12200 | Dermtech San Diego, CA Clinical Laboratory Scientist BS in biochemistry, biology, genetics, or related Exp: 1-2 year(s) |
The successful candidate will ensure that complex molecular diagnostic assays and systems are performed under appropriate CLIA compliance and regulatory requirements. The Clinical Laboratory Scientist independently performs clinical lab testing and other scientific examinations, record appropriate test documentations, and evaluates test results. Essential Duties and Responsibilities: Perform extraction techniques involving DNA/RNA, PCR and RT-PCR reactions, qPCR and RNA/DNA sequencing. Identify problems that may affect test performance or results and, following established protocols, correct problems or escalate to Clinical Laboratory Manager, technical supervisor, clinical consultant or lab director. etc. | 2/25/2020 |
| 12201 | Dicerna Lexington, MA Research Associate - RNAi Discovery BS/MS Exp: 0-5 years |
Dicerna Pharmaceuticals is looking for a BS/MS Research Associate to help in its drug discovery efforts. This is a hands-on research position that requires strong expertise in molecular and cellular methodologies. This is a full-time position. Dicerna offers an exciting work environment and strong team culture. Our company has a competitive benefits package and bonus incentive program. etc. | 2/25/2020 |
| 12202 | Digirad Bismarck, ND PET/CT Technologist AS/AA Exp: 6-12 months |
The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc.The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc.The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc. | 2/25/2020 |
| 12203 | Digirad El Paso, TX PET/CT Technologist AS/AA Exp: 6-12 months |
The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc.The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc.The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc. | 2/25/2020 |
| 12204 | Digirad Ft. Harrison, MT Tech Assistant HS diploma or equivalent Exp: 1 month |
The Technologist Assistant supports the technologist with various duties including transporting patients between the facility and scanner and completing paperwork. Essential Functions: 1. Assisting the technologist with patient care by transporting patients between the facility and scanner; sanitizing and cleaning patient care and staff areas; changing table linens; entering exam and patient information electronically or on paper; and answering the telephone. 2. Demonstrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. 3. Demonstrates knowledge and skills necessary to provide care appropriate to the age of the patients served. etc. | 2/25/2020 |
| 12205 | DiscGenics Salt Lake City, UT Purchasing Assistant / Receptionist AS/AA in business administration or similar Exp: 1+ year(s) |
DiscGenics is a clinical stage biotechnology company performing studies to support the continued development of our cell therapy products to treat diseases of the spine. We are seeking a full time Purchasing Assistant who will fulfill a dual role as a Receptionist. The qualified candidate must be friendly, professional and detail oriented with the ability to prioritize purchasing tasks as requested by our laboratory and office personnel. Responsibilities: Create purchase orders as directed. Communicate with vendors, including placing orders and some price negotiation. Work with quality department to track qualification requirements and status of vendors and raw materials. etc. | 2/25/2020 |
| 12206 | DiscGenics Salt Lake City, UT Quality Engineer BS in a relevant field Exp: 1+ year(s) |
DiscGenics is seeking an independently-driven quality engineer capable of implementing Quality Management System (QMS) processes in accordance with applicable country regulations and standards for biologics, pharmaceuticals, and medical devices. The quality engineer will also support new product development efforts including design control and risk management. Responsibilities: Serves as the voice of quality during the product design and development process. Facilitates risk assessment activities. Defines and implements the Quality Management System processes in accordance with 21 CFR 210/211, 21 CFR 820, 21 CFR 1271, including CAPA, training, internal audits, supplier controls, etc. etc. | 2/25/2020 |
| 12207 | DiscGenics Salt Lake City, UT Manufacturing Operator I HS diploma Exp: Entry level |
Discgenics is a clinical stage biotechnology company that is developing a patented disc cell therapy product to help patients suffering from degenerative diseases of the spine. DiscGenics is seeking a Manufacturing Operator l. The Manufacturing Operator l is an entry level position; as a Manufacturing Operator l, your duties will include maintaining cleanroom standards along with controlled environments. The position will require supporting the DiscGenics internal manufacturing team to ensure the clinical production of cell therapies and routine maintenance and cleaning of rooms and equipment. In addition, maintains records and cleanroom environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). etc. | 2/25/2020 |
| 12208 | DiscGenics Salt Lake City, UT AM Lab Associate BS in a biological or chemical field Exp: 1+ year(s) |
DiscGenics is a clinical stage biotechnology company performing studies to support the continued development of our cell therapy products to treat diseases of the spine. We are seeking a laboratory associate who can support the analytical team in developing, qualifying and performing a variety of cellular and chemical test methods. This is an entry level laboratory position that will provide experience with cell culture and cell characterization methods. The ideal candidate will be hard working and enthusiastic about our mission to aid patients with disc degeneration and have some experience with cell culture, cell based assays and/or laboratory automation. etc. | 2/25/2020 |
| 12209 | DNA Diagnostics Center Irving, TX Sales Associate (Direct to Consumer) unspecified Exp: 1-2 year(s) |
DDC is growing rapidly, and our customers need fast and accurate solutions for their life-changing challenges and questions related to paternity or other family relationships. The role of the Sales Representative (Direct to Consumer) is DDC’s premier sales position. From 8am to 8pm Monday through Friday, our global customers call us for answers about relationships that they use for immigration, surrogacy, or simply confirming the father of a child. The successful candidate for this role determines the services our clients require, charts their course through the testing process, and closes the sale. Income is not capped, and six-figure upside is achievable—it is determined by your own skills and motivation. etc. | 2/25/2020 |
| 12210 | DNA Diagnostics Center Gardena, CA Sales Associate (Direct to Consumer) unspecified Exp: 1-2 year(s) |
DDC is growing rapidly, and our customers need fast and accurate solutions for their life-changing challenges and questions related to paternity or other family relationships. The role of the Sales Representative (Direct to Consumer) is DDC’s premier sales position. From 8am to 8pm Monday through Friday, our global customers call us for answers about relationships that they use for immigration, surrogacy, or simply confirming the father of a child. The successful candidate for this role determines the services our clients require, charts their course through the testing process, and closes the sale. Income is not capped, and six-figure upside is achievable—it is determined by your own skills and motivation. etc. | 2/25/2020 |
| 12211 | DNA Diagnostics Center Fairfield, OH Sales Associate (Direct to Consumer) unspecified Exp: 1-2 year(s) |
DDC is growing rapidly, and our customers need fast and accurate solutions for their life-changing challenges and questions related to paternity or other family relationships. The role of the Sales Representative (Direct to Consumer) is DDC’s premier sales position. From 8am to 8pm Monday through Friday, our global customers call us for answers about relationships that they use for immigration, surrogacy, or simply confirming the father of a child. The successful candidate for this role determines the services our clients require, charts their course through the testing process, and closes the sale. Income is not capped, and six-figure upside is achievable—it is determined by your own skills and motivation. etc. | 2/25/2020 |
| 12212 | Mylan Pharmaceuticals Greensboro, NC Quality Technician, Inspections- 1st Shift BS/BA Exp: 0-2 years |
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help: Coordinate release documents, perform product releases in SAP, and perform product inspections. Write specifications and SOP’s, perform warehouse investigations, review rejections, place products on quality hold, process sample requests, returned goods and donations, ship studies, and review temperature data. Deliver and create training and help maintain training records. etc. | 2/25/2020 |
| 12213 | Durect Birmingham, AL Manufacturing Associate I HS diploma/BS/BA Exp: 0-2 years |
To conduct manufacturing and polymer development tasks. MAIN DUTIES AND RESPONSIBILITIES: Perform manufacturing/synthesis under GMP. Clean GMP equipment. Assist in polymer manufacturing equipment calibration and maintenance. Assist in equipment qualification studies, including documentation of studies. Assist in performance of R&D development programs. etc. | 2/25/2020 |
| 12214 | Editas Medicine Boulder, CO Research Associate II/Senior Research Associate, Analytical Chemistry MS in a life science Exp: 1-2 year(s) |
This new role on the Analytical Chemistry team in Boulder provides a unique opportunity to contribute to Editas’ efforts through the development of the analytical characterization of guide RNAs (identity, purity, stability), mainly in support of Process Development Team in Boulder. Key Responsibilities: Work closely with the Process Development group at the Boulder Colorado site to develop analytical methods and solve technical problems. Develop, execute, and qualify/validate methods for analytical characterization of oligonucleotides (identity, purity, impurity characterization, stability). etc. | 2/25/2020 |
| 12215 | Elpis Biopharmaceuticals Lexington, MA Research Associate, Biology & Functional Assays BS/MS in a related biological field Exp: 1-3 year(s) |
We are looking for a research associate to joint the biology and functional assay group. This group will analyze and screen newly discovered therapeutic molecules for biochemical, cellular and immunological function. The candidate will be responsible for efficiently delivering high-quality research results for decision making. The candidate will also help explore and develop innovative technologies to advance biologic projects. The candidate will analyze scientific results, provide oral and written reports, and remain current to literature reports and technological developments. Specific Responsibilities: Care for and scale up cancer cell lines for experiments. | 2/25/2020 |
| 12216 | Encoded South San Francisco, CA Scientist I/II, Assay Development BS/MS in a relevant science Exp: 1-2 year(s) |
This is a unique opportunity to work at the intersection of genomics and therapeutics and participate in the development of a diverse therapeutic pipeline driven by a transformative core technology. The position of Scientist I/II, Assay Development is part of the PD Analytics team and will assist the Process Development group in developing novel assays and supporting existing analytical assays used to characterize gene therapy products and processes in our pipeline. An ideal candidate will have experience in a drug development environment, analytics for viruses and viral vectors and well-versed in assay development and qualification. etc. | 2/25/2020 |
| 12217 | Endologix Irvine, CA Quality Assurance Technician HS diploma or equivalent Exp: Entry level |
Performs audits, inspections, configuration checks, and functional testing of in-process materials, parts and subassemblies used in the manufacture of partially assembled or finished medical devices. Responsible for assuring that the company’s products have been manufactured, inspected and tested using company approved procedures documents and equipment. Work with R&D, Manufacturing, and Quality to implement solutions to quality related problems. Coordinates, initiates, and implements Document Change Orders. Reviews quality records to ensure completeness and compliance to applicable quality procedures. etc. | 2/25/2020 |
| 12218 | Enzo Farmingdale, NY Production Associate I AS/BS in biology or related Exp: 0-2+ years |
This position is responsible for the timely and efficient scheduling and packaging of standard and custom products, and for providing support to other areas of manufacturing to ensure timely product delivery. Responsibilities: Assist in all packaging and labeling operations for Manufacturing. Assist in cGMP material inspection and receiving raw materials for Manufacturing. Maintain and organize the physical inventory of purchased and in-house materials. Assist in creating and maintaining electronic copies of all manufacturing documents. etc. | 2/25/2020 |
| 12219 | Epitopix Wilmar, MN Production Technician HS diploma/AS Exp: 0-2 years |
As a key member of the fermentation department the fermentation technician is responsible for the growth of bacteria used to create vaccines based on proprietary SRP technology. This critical role will be engaged in production, process improvement, and the support functions necessary to ensure vaccine delivery to hundreds of customers throughout North America and the world. SRP technology is critical to the maintenance of the global food supply and the fermentation technician is truly in on the ground floor. etc. | 2/25/2020 |
| 12220 | Eton Boston, MA Lab Technician BS in biology, biotechnology, or related life science Exp: 6 months |
Collect and analyze DNA samples to determine sample quality and concentration. Design and process DNA sequencing polymerase chain reactions (PCR) using DNA samples submitted by customers, and perform dye-terminator purification of the completed DNA sequencing reactions. Produce data files to load onto the Applied Biosystems 3730xl DNA Analyzer. Troubleshoot common problems the customers are having with their DNA sequencing. | 2/25/2020 |
| 12221 | Eurofins Lancaster, PA 2nd shift - Data Review Specialist - Mycoplasma Services BS in microbiology, biology, or related Exp: 1-3 year(s) |
Employee Responsibilities: Ensures that our clients receive quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations. The Ideal Candidate would possess: Strong computer, scientific, and organizational skill. Excellent communication (oral and written) and attention to detail. Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude. Ability to learn new procedures, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies. | 2/25/2020 |
| 12222 | Eurofins Lancaster, PA 2nd shift - Associate Microbiologist BS in microbiology, biology, or related Exp: Not necessary for BS candidates |
Employee Responsibilities: Perform analyses for bio/pharmaceutical microbiology (routine and non routine). Review and evaluate raw data for acceptability. Set up and validate new analytical or related processes used by the department. Perform collection of water/EM samples when required. The Ideal Candidate would possess: Strong computer, scientific, and organizational skills. Excellent communication (oral and written) and attention to detail. etc. | 2/25/2020 |
| 12223 | Exactech Gainesville, FL Clinical Research Associate HS diploma/BS/BA Exp: 1 year |
Duties and Responsibilities (Key Deliverables): 1. Monitor the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), GCP, and all applicable regulatory requirements. 2. Conduct visits to assess the qualification of potential investigative sites, initiate sites, instruct site personnel on the proper conduct of studies and use of Electronic Data Capture (EDC) system, review and ensure accuracy of data collected, and terminate studies. 3. Monitor data submitted to the EDC system, perform source document verification, retrieve and/or ensure appropriate electronic submission of Case Report Forms (CRFs), and perform query resolution in a timely manner. 4. Ensure sites report adverse events according to protocol specifications. 5. Assist investigative sites with obtaining and maintaining Institutional Review Board (IRB)/Ethical Committee (EC) approval. etc. | 2/25/2020 |
| 12224 | Exactech Gainesville, FL Surgical Services Technician HS diploma or equivalent Exp: 1 year |
Duties and Responsibilities (Key Deliverables): 1. Process loaner/instrument returns: sterilization, cleaning, completing required forms, updating the inventory control system, performing functional checks, and restocking. Initiate the processing of those instruments that do not satisfy the quality standards (Non-Conforming instruments). Refer complaints of service or product failure to appropriate departments. 2. Perform minor repairs on instruments and provide disposition of obsolete or worn instrumentation in accordance with established procedures. 3. Stock instrument storage bins. 4. Assist in the filling of orders. 5. Provide on call services as necessary. etc. | 2/25/2020 |
| 12225 | Exonbio San Diego, CA Research Associate MS in biology Exp: 1 year |
We are looking for a RESEARCH ASSOCIATE to join our antibody development team. Requirements: Master Degree in Biology. One year experience in Cell culture and banking, PCR, Protein purification with AKTA. | 2/25/2020 |
| 12226 | Exsurco Wakeman, OH Assembly Technician HS diploma Exp: 3 months |
Primary role is to perform all forms assembly activities including equipment setup and tear down where required as well as in-process verifications. In addition, this position includes several cross-functional responsibilities comprising Shipping, Receiving, Job Picking, Warehousing and Plant Cleaning and some Maintenance activities. This position also has responsibilities associated with Servicing returned products (disassembly and reassembly, diagnosis and report writing). Will be working 20 – 24 hours a week. etc. | 2/25/2020 |
| 12227 | Facet Medical Technologies Atlanta, GA Quality Engineer BS in engineering, science, or related Exp: 1-3 year(s) |
The Quality Engineer plans and directs activities concerned with development, application, and maintenance of quality processes, materials, and products. Additionally, responsible for investigation manufacturing and customer nonconformance’s, determining root causes and corrective actions, reviewing and approving protocols and final reports and developing product specifications and sampling plans. etc. | 2/25/2020 |
| 12228 | Fate Therapeutics San Diego, CA Associate Scientist/Senior Research Associate BS/MS in a biological science Exp: 1+ year(s) |
Fate Therapeutics is seeking a motivated professional with analytical assays experience to support Fate’s clinical and manufacturing process development programs. The successful candidate will execute and analyze experiments to assess the characteristics of hematopoietic and stem cell-based therapeutics under cGMP environment. Candidates must have experience working with mammalian cell culture, and analysis of data from flow cytometry, cell-based assays, or PCR assays. This is a full-time position located at our corporate headquarters in San Diego, California reporting to the Senior Manager, QC. etc. | 2/25/2020 |
| 12229 | Finch Somerville, MA Research Associate, Process Development BS in chemical engineering, biomedical engineering, or chemistry Exp: 0-2 years |
Responsibilities: Plan, execute, and document studies related to design of novel drug products. Support scale-up and technical transfer of production processes to GMP Manufacturing. Assist with troubleshooting, root cause analysis, and identification of corrective actions to support Pharmaceutical Development or GMP Manufacturing equipment and process issues. Work cross-functionally across Quality, Research, Clinical, and Manufacturing teams to achieve company goals. etc. | 2/25/2020 |
| 12230 | Flexion Therapeutics Field, Flex Sales Representative BS/BA Exp: 1-3 year(s) |
Considering a new job and company is a really big decision. Typical job descriptions don't really give you a sense of what a job is actually like. When considering a Flex Sales role at Flexion, we want you to see why this opportunity is so amazing, the impact you'll have and what the company and culture are really like. Why this role is different: First, let's talk why this role is different from other sales roles and what you'll get to do: The name says it all. Flex means it's a mix of inside sales and in person sales. This role is a fantastic way for driven, passionate and resilient individuals earlier in their career to gain experience. You'll manage daily sales call activity, with the purpose of influencing customers and increasing sales. etc. | 2/25/2020 |
| 12231 | Cytek Biosciences Fremont, CA Research Assistant - Flow Cytometry - Reagent Development BS in chemistry, biology, or other life sciences Exp: None required |
We are currently seeking a Research Associate for our Reagent Development Group. This individual will work with other scientists in the group to identify and evaluate antibodies and fluorescent dyes for developing flow cytometry reagents. Conduct immunological conjugation with different antibodies and fluorophores. Perform routine analysis of reagent using chromatographic spectrophotometer, HPLC and flow cytometry technique. Follow SOPs, policies and regulations and performing routine lab equipment maintenance. etc. | 2/24/2020 |
| 12232 | Cytel Waltham, MA Financial Analyst BS/BA in finance or accounting Exp: 1-3 year(s) |
We are experiencing exponential growth on a global scale and hiring Financial Analyst to join our Finance division. Summary of Job Responsibilities: As the Finance Analyst supporting Project Leadership Team, you acquire an understanding of the project economics and profitability drivers. Under supervision, you will assist in translating them into operational actions, and proactively advising the PL on how to influence critical operational levers in order to positively impact project financials. Key Responsibilities include: Create accurate, transparent, and timely financial analysis to support project leadership in project decision making process; etc. | 2/24/2020 |
| 12233 | CytomX Therapeutics South San Francisco, CA Senior Research Associate, Upstream Process Development MS in biochemistry, molecular biology, or cell biology Exp: 0-3 year(s) |
Professional Responsibilities: Operation and harvest of stirred-tank bioreactors (2-50 L, fed-batch). Performance of fed-batch cell culture studies in shake flasks or micro-bioreactors. Titer analysis using ForteBio Octet, occasional performance of other assays as-needed. Experimental design and analysis, commensurate with experience. Authorship or contribution to SOPs and development reports. Support of GMP mfg; may include BPR review and PIP duties. etc. | 2/24/2020 |
| 12234 | Cytovance Oklahoma City, OK Facilities Technician I HS diploma or equivalent Exp: Entry level |
The Facilities Technician is integral to successful biologics manufacturing and to product safety. The Facilities technician maintains, calibrates, and operates equipment and utilities in an FDA-regulated environment. This is an entry level position, On the Job training will be provided. ESSENTIAL DUTIES AND RESPONSIBILITIES: Completes all scheduled maintenance and calibration activities on time. Each month, evaluates assigned workload and manages time to complete the work (ex. ordering/gathering supplies, coordinating with other departments for equipment availability, etc.). Ensures documentation of all activities is completed in compliance with company procedures. etc. | 2/24/2020 |
| 12235 | Cytovance Oklahoma City, OK Upstream Manufacturing Associate AS in science or biotech Exp: 1-2 year(s) |
Executes upstream manufacturing of clinical and commercial products. Executes pre and post processing activities such as: clean of production equipment, including the operation of automated bioreactor, harvest and media prep skids. This position is accountable for executing the manufacturing processes in Contract Manufacturing Facility and/or Master Cell Banking Facility. The hours for this role will be the swing/night shift. Shift differential pay is available. ESSENTIAL DUTIES AND RESPONSIBILITIES: Ability to work with bioreactor operation and cell culture including aseptic technique. Execute and monitor critical processes supporting mammalian, microbial, and fill finish production facilities. Solid experience with the following: large-scale centrifuges, washers, autoclaves. etc. | 2/24/2020 |
| 12236 | Cytovance Oklahoma City, OK Solution Prep Associate I HS diploma/AS Exp: 1-2 year(s) |
This position is accountable for producing and delivering large and small-scale media and buffers to support Upstream and Downstream Manufacturing Operations. ESSENTIAL DUTIES AND RESPONSIBILITIES: Batching and delivering both large and small-scale media and buffer batches. Assisting in the review & creation of operation documents by providing input to technical composition of documents. Effectively demonstrate understanding of GMPs & how it applies to specific responsibilities. Following accurate oral & written procedures in operating production equipment & performing processing steps. Maintain orderliness of process area. etc. | 2/24/2020 |
| 12237 | Day Zero Diagnostics Boston, MA Research Lab Associate BS in molecular biology, biochemistry, or microbiology Exp: 1 year |
Day Zero Diagnostics is an infectious disease genomics start-up in Boston that is seeking a highly motivated full-time Laboratory Research Associate. The employee will become an integral member of our dynamic team as we develop a novel rapid diagnostic to provide the species ID and antibiotic resistance profile. We value intellectual curiosity and a strong work ethic. Job Duties: Perform and assist with molecular biology and microbiology experiments to support diagnostic development. Work closely with other Research Scientists and Associates to design and execute experiments. etc. | 2/24/2020 |
| 12238 | Demetrix Berkeley, CA Associate Scientist/ Sr. Associate Scientist, Strain Engineering BS Exp: 1-4 year(s) |
Demetrix is a start up in the San Francisco Bay area that is making nature’s medicines in a smart and responsible way. We are seeking an Associate Scientist/Senior Associate Scientist to assist the Strain Engineering team. The individual in this role will be part of an interdisciplinary team of molecular biologists, fermentation scientists and engineers, automation engineers, software engineers, and analytical chemists working to rapidly develop microbial strains to produce natural product medicines. etc. | 2/24/2020 |
| 12239 | Denison Lincoln, RI Compounder, Lincoln HS diploma or equivalent Exp: 1 year |
The successful candidate for the position of Manufacturing Operator shall be fully capable of performing all job functions listed: Job Tasks: Submitting a requisition for raw materials. Verifying the clean status of all equipment and utensils prior to use. Batch pre-staging operations. Weighing and blending raw materials. Following manufacturing instructions. Documents production by completing forms, reports, logs, and records of equipment and batches. etc. | 2/24/2020 |
| 12240 | Synexus Pinellas Park, FL Clinical Research Coordinato BS/BA in health sciences Exp: 1 year in clinical research |
Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements. Coordinate and conduct patient care visits (drawing blood, collecting vital signs, performing ECG’s and processing specimens) and assure all procedures are conducted in compliance with the clinical protocol. | 2/23/2020 |
| 12241 | Synexus Dalas, TX Clinical Research Study Nurse BS/BA in health sciences Exp: 6+ months clinical research experience |
Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements. Responsible for completion of all study documentation forms, including case report forms and other study specific documents. | 2/23/2020 |
| 12242 | Synexus Columbus, OH Patient Services Assistant HS Diploma/GED Exp: 1 year as receptionist/office coordination |
Manages the front desk activities of the site office. Schedules subjects for study visits, enters information in clinical conductor system, and conducts appointment reminders; Provide support for filing, mailings, copying, collating, ordering, etc. | 2/23/2020 |
| 12243 | Sun Pharma Billerica, MA Microbiology Technician I HS Diploma/GED Exp: 1+ years related experience |
Performs routine microbiological sampling and quality control testing supporting manufacturing of commercial pharmaceutical products in accordance with current Good Manufacturing Practices (cGMP), ISO and Pharmalucence policies and procedures | 2/23/2020 |
| 12244 | Sun Pharma Billerica, MA Formulation and Fill Technician I HS Diploma/GED Exp: 0-2 years related experience |
Performs the formulation and dispensing of pharmaceutical products according to current Good Manufacturing Practices (cGMPs) and utilizing Standard Operating Procedures (SOPs) in a clean room environment. Formulate and dispense product in a clean room environment for Radio-pharm as well as dermatological products. Wash and sterilize all equipment, tubing, filters, stoppers, vessels, vials, ampoules etc. | 2/23/2020 |
| 12245 | Sunrise Pharma Rahway, NJ Manufacturing Operator HS Diploma/GED Exp: 0-2 years related experience |
Candidate should have knowledge of manufacturing procedures, good manufacturing systems and familiarity with regulatory and Standard Operating Procedures. Experience in granulation, milling, compression, and encapsulation. Conformance to GMP and SOP requirements by following batch records accurately in granulation, encapsulation, and compression. Perform setup, cleaning and troubleshooting of encapsulation machines and tablet presses. Demonstrated ability to read and interpret documents such as operating and maintenance instructions and procedure. Experience in a pharmaceutical or bio pharmaceutical environment. | 2/23/2020 |
| 12246 | Scanlan St. Paul, MN Surgical Instrument Spec. Order Fulfilment HS Diploma/GED Exp: 0-2 years related experience |
The Surgical Instrumentation Specialist/Order Fulfillment position is responsible for preparing instruments for etching, building wet labs, maintaining demonstration cases, filling orders for repairs and reconditions, repairing and modifying surgical instruments, operating and maintaining equipment, continuous work space cleaning and upkeep, any other duties as requested by supervisor. | 2/23/2020 |
| 12247 | Surrozen South San Francisco, CA Research Associate, Protein Sciences -Protein Expression/Purification BS or MS in protein biochemistry or related Exp: 1-4 years lab experience (class, internship, academic) |
The Research Associate position for Protein Expression/Purification within the Protein Sciences Group is a great opportunity for experienced associates as well as recent graduates to expand their skills in state-of-the-art biochemical techniques while accelerating therapeutic discovery and development in regenerative medicine. Characterize and purify protein samples using SDS-PAGE, chromatography, and related techniques. Perform mammalian cell transfections for recombinant protein expression | 2/23/2020 |
| 12248 | Surrozen South San Francisco, CA Research Associate, Protein Sciences - Molecular Biology/Protein Expression BS or MS in protein biochemistry or related Exp: 1-4 years lab experience (class, internship, academic) |
Produce recombinant DNA clones and plasmids using standard molecular biology protocols. Perform small scale transfection in mammalian cells for recombinant protein expression. Characterize purified protein samples by SDS-PAGE and related techniquques. Preparation of presentations, technical reports, summaries and detailed protocols, and contribute to company reports as requested | 2/23/2020 |
| 12249 | Surrozen South San Francisco, CA Research Associate - Senior Research Associate, In vivo Pharmacology BS or MS in molecular/cell biology, biochemistry, genomics, etc. Exp: 1+ years research experience |
Help develop and implement disease and injury models for characterization of lead molecules. Conduct independent in vivo studies and contribute to collaborative activities. Perform tissue necropsy. Perform tissue sample analysis, such as clinical biochemistry, ELISA, qPCR and immunohistochemistry. Maintain mammalian cell culture, perform gene expression studies and in vitro functional assays (e.g., RT-qPCR, reporter assays, FACS analysis). | 2/23/2020 |
| 12250 | Surrozen South San Francisco, CA Research Associate-Senior Research Associate, Biochemistry/Biophysics BS or MS in biochemistry, biophysics or related Exp: 1+ years research experience |
Perform high-throughput biophysical and biochemical assays to evaluate developability properties of antibody-based molecules. Perform routine cell-culture maintenance, protein expression in mammalian cells and purification in milligram-scale protein production and characterize antigen:antibody (Fab) complexes for crystallization screens. | 2/23/2020 |
| 12251 | Surrozen South San Francisco, CA Research Associate, Discovery Biology BS or MS in molecular/cell biology, biochemistry, genomics, etc. Exp: 1-4 years lab experience (class, internship, academic) |
Establish relevant mammalian cell or organoid cultures, study gene expression and perform in vitro functional assays (e.g., RT-qPCR, reporter assays, FACS analysis). Study cell fate in organoids and tissue explants. Investigate gene expression in tissue samples by RT-qPCR, RNA in situ hybridization (RNAscope@), Western blots, ELISA and immunohistochemistry. | 2/23/2020 |
| 12252 | Sutro Biopharma San Carlos, CA Manufacturing Associate BS in biological sciences Exp: 1-6 years in cGMP manufacturing |
Perform various manufacturing tasks such as operating, troubleshooting, sterilizing, maintaining, preparing, and cleaning of various process equipment such as stirred-tank bioreactors, media/buffer solutions, disc stack centrifuges, homogenizer, pelletizer, dryer, TFF skid, chromatography systems, parts washers, and CIP systems, under the guidelines of established SOPs and cGMP regulations. Reliably and consistently execute well defined SOPs and batch records. Accurately document data and complete batch records. | 2/23/2020 |
| 12253 | Sutro Biopharma San Carlos, CA Quality Control Associate MS in chemistry, biochemistry, bioanalytical chemistry or scientific related Exp: 1-3 years |
Perform analytical assays on daily basis. The assays include wet-lab chemistry, HPLC, CE, icIEF, ELISA, Electrophoresis, UV spectroscopic based methods, and compendial methods required for the release and stability testing of water, raw material, in-process, and final products. Perform data review and analysis. Support method transfer and validation activities | 2/23/2020 |
| 12254 | Suvoda Conshohocken, PA Associate Project Manager - Entry Level BS/BA in life or computer sciences Exp: Entry Level |
Work as part of a cross-functional project team responsible for the delivery of Interactive Response Technology (IRT) for randomization and drug supply management in clinical trials. Support the Services Delivery project team in:Liaising with the client to discuss requirements, handle issues, provide status updates, and answer questions. Designing the IRT solution to meet the study requirements based on the clinical protocol, Suvoda proposal and discussions with the client | 2/23/2020 |
| 12255 | Suvoda Portland, OR Associate Project Manager - Entry Level BS/BA in life or computer sciences Exp: Entry Level |
Work as part of a cross-functional project team responsible for the delivery of Interactive Response Technology (IRT) for randomization and drug supply management in clinical trials. Support the Services Delivery project team in:Liaising with the client to discuss requirements, handle issues, provide status updates, and answer questions. Designing the IRT solution to meet the study requirements based on the clinical protocol, Suvoda proposal and discussions with the client | 2/23/2020 |
| 12256 | Suvoda Portland, OR Quality Control Analyst BS/BA Exp: 1-3 years |
Ensure activities and deliverables are performed during the software development process as required by Suvoda procedures. Identify issues during the development of a product (or delivery of a service) before it is released. Release Suvoda products and systems through the various phases of development. Review and approve SDLC and validation deliverables | 2/23/2020 |
| 12257 | Suvoda Conshohocken, PA Quality Assurance Analyst BS/BA Exp: 1-3 years |
Manage and monitor quality assurance activities, such as the review and approval of QMS documents, investigation of issues and execution of CAPAs, preparation and conduct of audits, training management and the qualification of 3rd party vendors. Perform issue trending and work with the organization to improve processes to prevent issues from occurring during the development of products and delivery of services | 2/23/2020 |
| 12258 | SVA Brookfield, WI Client Relations Specialist (CRS) HS Diploma/GED Exp: 1-2 years in financial institution preferred |
The CRS provides operational, administrative, and clerical support to the financial advisors in our Brookfield office. This role requires the ability to work at a fast pace and be able to multitask while differentiating tasks on level of importance, urgency, and estimated time of completion. Assist with client onboarding which includes preparing new account paperwork, opening accounts, and transitioning new assets. | 2/23/2020 |
| 12259 | Sword Bio Carmel, IN Research Associate I BS/BA in biology, biochemistry or related Exp: 1-3 years lab experience |
Plan experiments with guidance from supervisor. Perform complex and critical laboratory experiments (primarily ELISA) with accuracy and precision. Analyze experiment results and recommend potential follow-on experiments. | 2/23/2020 |
| 12260 | Synexus Anderson, SC Research Associate BS or Certified Medical Assistant Exp: 1 year in clinical research |
Assists the Clinical Research Coordinators in their responsibilities by doing the following: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Assists the Clinical Research Coordinators with updating and maintaining logs and filing in charts;Perform basic lab procedures, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up, | 2/23/2020 |
| 12261 | Synexus Chicago, IL Clinical Research Coordinator BS/BA in health sciences Exp: 6+ months clinical research experience |
Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements. Responsible for completion of all study documentation forms, including case report forms and other study specific documents. | 2/23/2020 |
| 12262 | Synexus St. Louis, MO Research Associate BS or Certified Medical Assistant Exp: 1 year in clinical research |
Assists the Clinical Research Coordinators in their responsibilities by doing the following: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Assists the Clinical Research Coordinators with updating and maintaining logs and filing in charts;Perform basic lab procedures, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up, | 2/23/2020 |
| 12263 | STAAR Surgical Monrovia , CA Quality Control Inspector II HS Diploma/GED Exp: 1 year with computers |
Perform force and functional testing and data calculations for injector cartridges. Perform QA review of Device History Records. Maintain Device History Records. Inspect, sort, disposition and transfer of returned product from receiving dept., mail, customer service or other. | 2/22/2020 |
| 12264 | STAAR Surgical Monrovia , CA Production Technician (CNC) HS Diploma/GED Exp: 1-2 years in IOL, contact lense, or medical devices |
Thorough knowledge of all applicable SOP's: makes proper decisions in line with applicable SOPs and standards under normal conditions. Perform highly technical tasks in support of manufacturing including equipment set-up and manufacturing of product, tool changes, sterilization processes, and filtration of material and calibration activities as assigned. Troubleshoot issues on equipment and assist with preventative maintenance. | 2/22/2020 |
| 12265 | STAAR Surgical Monrovia , CA Production Operator I HS Diploma/GED Exp: 1-2 years in medical devices |
Thorough knowledge and appropriate implementation of basic production functions. Completes required production documentation accurately. Consistently meets quality and productivity targets. Appropriately follows company policies, rules, and regulation | 2/22/2020 |
| 12266 | Starkey Hear Technologies Eden Prairie, MN Microelectronic Mfg Engineer I BS/BA in engineering or physical sciences with emphasis in metrology/engineering Exp: 1-3 years in process/manufacturing engineering |
We are seeking to add a Microelectronic Manufacturing Engineer that will investigate and develop new microelectronic technologies and processes. In addition to new development work, this position is also responsible for improvements of existing assembly processes. This involves developing, prototyping, implementing and improving new thick film ceramic substrate, hybrid assemblies and PCB/flexible circuit surface mount assembly manufacturing processes required for both new product introductions and existing products. | 2/22/2020 |
| 12267 | Starkey Hear Technologies Eden Prairie, MN Test Engineer I - New Products BS/BA in engineering/physical sciences Exp: 0-3 years with electronic hardware/software |
Design, develop, and implement automated systems to test product in a manufacturing environment, at component, subassembly and systems levels. Perform product requirements analysis, test requirements definition, test system hardware and software design, systems integration, and validation. Generate design, validation, and maintenance documentation to comply with corporate quality system and department policies | 2/22/2020 |
| 12268 | Starkey Hear Technologies Eden Prairie, MN Firmware Engineer I MS in electrical engineering Exp: 1+ years |
Starkey Hearing Technologies is seeking a talented Firmware Verification Engineer to join the Firmware Engineering Department. The Firmware Engineering Department at Starkey Hearing Technologies is responsible for architecting, developing, and verifying firmware for DSPs and microcontrollers that define the core functionality of millions of hearing products shipped worldwide. | 2/22/2020 |
| 12269 | Starkey Hear Technologies Eden Prairie, MN Electrical Engineer I - EA Engineering BS/BA in electrical engineering Exp: 1 year in product development |
Generate component requirements and review and contribute to system performance requirements. Lead the Electro-Acoustic Engineering team in documenting specific requirements in the SyRS’s and the SDR’s using the Hardware Development Hearing Aid Design Guide as a high-level reference. Work with the Project Manager to manage work efforts to ensure project schedules are met and areas of high risk are identified and mitigated with appropriate risk mitigation plans. Follow the Electroacoustic Engineering Product Development Process. Perform electrical and electro-acoustic design tasks and provide input into project timelines and schedules. | 2/22/2020 |
| 12270 | Starkey Hear Technologies Eden Prairie, MN Software Tester I BS/BA Exp: 1-2 years in software test/quality assurance |
Conduct Software Testing on software applications. Follow standard Configuration Management practices and utilize a defect tracking tool. Tracking quality assurance metrics such as defect densities and open defect counts. Perform system level testing on Starkey’s Software and Hardware systems working either in a team or independently. | 2/22/2020 |
| 12271 | Starkey Hear Technologies Eden Prairie, MN Test Engineer I - New Products BS/BA in electrical/mechanical/computer engineering Exp: 0-3 years with electronic hardware/software |
Design, develop, and implement automated systems to test product in a manufacturing environment, at component, subassembly and systems levels.Perform product requirements analysis, test requirements definition, test system hardware and software design, systems integration, and validation. Generate design, validation, and maintenance documentation to comply with corporate quality system and department policies | 2/22/2020 |
| 12272 | SDC Tempe, AZ Biostatistician MS in biostatistics/statistics Exp: 1-3 years |
Supports lead biostatistician on clinical studies; may serve as lead biostatistician with oversight from a more senior biostatistician. Maintains the statistical integrity of clinical trials analyzed by SDC. Assists in preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, and writing statistical sections of clinical study reports. | 2/22/2020 |
| 12273 | Stereotaxis Saint Louis, MO Field Service Engineer - (FSE.6) AS/AA in electronics Exp: 1-5 years in field service |
Provide on site and remote service and support of Stereotaxis magnetic navigation systems including permanent magnets, and servo control systems. Interface with customers and vendors to ensure a quality service experience and that all expectations are met. | 2/22/2020 |
| 12274 | Steripharma Syracuse, NY New! Warehouse Technician - 1st Shift HS Diploma/GED Exp: 1+ years in warehousing |
This position is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. | 2/22/2020 |
| 12275 | Steripharma Syracuse, NY Production, Clean Room Pharmaceutical Technician - 2nd Shift AS/AA or BS/BA Exp: 1+ years in hospital or manufacturing |
This position operates production equipment, to include non-sterile filling machines, and packaging and labeling machines. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. | 2/22/2020 |
| 12276 | Steripharma Syracuse, NY Sanitation and Custodial Services Technician, 3rd Shift HS Diploma/GED Exp: 1-2 years in production environment |
This position is responsible for performing a variety of duties in support of the maintenance of buildings, facilities, and grounds. Also, this position is responsible for a variety of cleaning duties, a variety of other building maintenance work, and related duties as assigned. Sweep and mop floors, clean windows; clean restrooms and fixtures; clean and maintains lunch and break rooms. Strip and wax tiled floors as required; vacuum, buff and wax floors. | 2/22/2020 |
| 12277 | Steris Coon Rapids, MN Validation Technician BS/BA Exp: 1 year in sterilization for medical devices |
The Validation Technician assists in the processing of Customer products, and coordinates production scheduling, validations and qualifications. Monitors, studies and controls the sterilization of medical devices and other items to ensure effective sterilization. Coordinates with Customers and Sales to provide quotations for validations. Works with Customers to complete validation timelines and Customer validation forms | 2/22/2020 |
| 12278 | Steris Keller , TX Quality Technician I HS Diploma/GED Exp: 1 year in medical devices |
Performs medical device evaluations and monitors the quality of outgoing medical devices. Evaluates incoming medical devices in accordance with procedure guidelines to accurately prepare service/repair estimates. Performs routine testing for product release. Validates accuracy of outgoing repair documentation. Provides feedback to QA and production departments concerning technician and product performance. | 2/22/2020 |
| 12279 | Steris Chicago, IL Sterile Processing Technician I HS Diploma/GED Exp: 1+ years in SPD |
Provides on-site support for the reprocessing of surgical instruments and trays to contracted facilities in compliance with the Department of Health, TJC, OSHA, CDC, AAMI and AORN standards and facilities goals and policies. Position level will be determined by previous job related experience, performance and certification requirements. | 2/22/2020 |
| 12280 | Steris Palo Alto, CA Field Service Representative I AS/AA or BS/BA in electronics or mechanical engineering Exp: 1-2 years related |
Position acts as Trusted Advisor to STERIS Customers in maintenance and procurement of medical devices and consumable products as part of a high performing team. Drive an exceptional Customer experience by providing on-site preventative maintenance, troubleshooting, repair, equipment modification and installation support on complex mechanical, electro-mechanical and electronic units in a high stress healthcare environment. Provide superior Customer service by pro-actively interacting and communicating with Customers. | 2/22/2020 |
| 12281 | Steris Birmingham, AL CNC Machinist I HS Diploma/GED Exp: 1+ years at CNC machine |
Operates both manual and CNC equipment for the efficient production of quality components. Responsible for the production of high-tolerance precision parts. Interpret technical prints. Setup, operate and adjust machining equipment for production efficiency with supervision. Monitors quality of parts produced to ensure customer requirements are met. | 2/22/2020 |
| 12282 | Steris Charleston, SC Technician HS Diploma/GED Exp: 1-3 months training/experience |
The primary role of the Repair Technician is to perform repairs on medical instrumentation. Technicians will be trained to become familiar with various types of surgical instruments and understand how to best maintain and repair them. Repairs are completed on a repair truck onsite at a hospital or surgery center. In addition to repair work, Technicians may work with a team including Sales Representatives and RCs (Repair Consultants/Managers) to identify and capitalize on revenue opportunities. | 2/22/2020 |
| 12283 | Steris Brooklyn Park, MN Quality Assurance Technician I Associates degree Exp: 1 year related role |
The Laboratory Quality Assurance Technician I position is applicable to contract laboratory, manufacturing (if applicable) and steam processing (if applicable). The position is responsible for day to day execution of the quality system including but not limited to record review and verification including laboratory reports and manufacturing and sterilization processing run records as applicable, maintenance of quality documents related to calibration, validation, software, logsheets, and training records as applicable. | 2/22/2020 |
| 12284 | Strand Therapeutics Cambridge, MA Associate Scientist I, Synthetic Biology BS or MS in biological engineering/science/chemistry Exp: 1-3 years research experience |
We are looking for people who have the enthusiasm andmotivation to be a highly contributing member of a small team. This opportunity will offer the employee the ability to work closely with the founding team, as well as to form closepartnerships with team members during the development and formation of the company. Executing molecular biology experiments including molecular cloning, bacterial transformation and mammalian cell culture. | 2/22/2020 |
| 12285 | Stratos Genomics Seattle, WA Research Associate/Scientist, Molecular Engineering MS or BS/BA in chemistry/chemical engineering or related Exp: 1-2 years lab experience |
Candidates will be involved in synthesizing the unique building blocks for our novel DNA sequencing technology, developing and optimizing synthesis protocols, as well as proposing and executing innovative experiments to push our technology forward. The position is salaried with hours dependent on lab needs and project deadlines. | 2/22/2020 |
| 12286 | Structure Medical Naples, FL Swiss CNC Machinist I HS Diploma/GED Exp: 1 or more years in programing/operating CNC machines |
Performs entry level specialized computer numerical control (CNC) machinist work for Structure Medical, LLC. Operates CNC machines to run production per approved schedule provided. Work is performed under close supervision with minimal latitude for the use of initiative and independent judgment. | 2/22/2020 |
| 12287 | Stryker Portage, MI Design Engineer - Mechanical BS/BA in mechanical engineering Exp: 0-3 years |
As a Design Engineer- Mechanical, you will work to develop innovative new products for the Surgical technologies group. A passion for innovation and creativity is desired for this role. Plan and conduct engineering research, design, development projects as assigned. Monitor and control progress of projects to ensure sound application of engineering principles are used and design intent is being followed/achieved | 2/22/2020 |
| 12288 | Stryker San Jose, CA Quality Engineer BS/BA in engineering Exp: 0+ years in regulated manufacturing environment |
As a Quality Engineer you will provide support in quality assurance, control, and preventative activities with a focus on continuous improvement of internal products and processes. You will own identified internal and supplier driven non-conformances and manage the timely closure of NC's within Trackwise. You will communicate with suppliers regarding non-conformances, escalating supplier corrective action, changes and process qualifications requests as required. You will engage in the development, improvement and sustaining of the internal manufacturing processes for existing and new products. | 2/22/2020 |
| 12289 | Stryker Plainfield, IN Quality Control Technician - 1st shift HS Diploma/GED Exp: 1-2 years in tolerance QC |
Will perform incoming inspection on components and Electro/mechanical products per company/regulatory specifications. Will work from engineering schematics or blueprints to perform accurate checks and tests. Will be required to comply with documentation and regulatory procedures and policies. Will work across multiple, different IT platforms and Quality Management Systems. Will interact with internal and external customers to resolve, inspection and/or components issues, across multiple divisions. | 2/22/2020 |
| 12290 | Stryker Davie, FL Assembly Technician I HS Diploma/GED Exp: 1 year experience |
"Responsible for providing assembly, testing and facility support for all our production efforts. Assembly of fabricated parts and assemblies at work stations along with testing of final assemblis to meet tolerances and product specifications. Uses hand tools and power tools to assemble units according to assembly / work instructions. | 2/22/2020 |
| 12291 | Stryker Leesburg, VA Entry Level Fulfillment Clerk HS Diploma/GED Exp: 1 year related experience/training |
Ensures complete fulfillment of all replenishment orders. Unloads daily shipment of incoming surgical sets and does the precautionary cleaning of incoming sets. Verifies kind and count of replenishments prior to shipping. Processes and stages outgoing replenishments. Performs the last check of replenishments and surgical sets prior to final boxing for shipment | 2/22/2020 |
| 12292 | Stryker Leesburg, VA Entry Level Fulfillment Clerk HS Diploma/GED Exp: 1 year related experience/training |
Ensures complete fulfillment of all replenishment orders. Unloads daily shipment of incoming surgical sets and does the precautionary cleaning of incoming sets. Verifies kind and count of replenishments prior to shipping. Processes and stages outgoing replenishments. Performs the last check of replenishments and surgical sets prior to final boxing for shipment | 2/22/2020 |
| 12293 | Smith + Nephew Memphis , TN Distribution Associate I HS Diploma/GED Exp: 0-1 years in distribution/logistics |
The Distribution Associate I will interact with the WMS, TMS, RF scanning and/or other warehouse equipment to perform intermediate level distribution tasks in accordance with defined job processes. They will perform these tasks with a focus on safety, quality and productivity. They must comprehend and demonstrate compliance with Standard Operating Procedures and work instructions. The Distribution Associate I is responsible for providing constructive input to enhance the work process and environment. | 2/17/2020 |
| 12294 | Smith + Nephew Memphis , TN Inspector Technician I HS Diploma/GED Exp: 0-2 years in product inspections |
Inspect raw materials, components, assembled product, semi-finished product & finished product per inspection procedures/drawings and to print specifications. Utilize attribute and variable measuring equipment/gauges as well as mating parts to determine as found/as left conditions of product. Review corresponding product documentation to verify acceptability per specification and QSR requirements | 2/17/2020 |
| 12295 | Smith + Nephew Columbia, MD Manufacturing Technician 1 AS/AA in life sciences Exp: 1-2 years in GMP environment |
Responsible for hands-on execution of all activities in the manufacturing area including the processing and packaging of human tissue products for transplantation. All duties are performed in compliance with FDA cGMP/cGTP requirements, American Association of Tissue Banks (AATB) standards, and Osiris Therapeutics Inc. standard operating procedures (SOPs). The candidate should have a commitment to high standards of quality | 2/17/2020 |
| 12296 | Smith + Nephew Memphis , TN Graduate Engineer BS in industrial/mechanical engineering Exp: Co-op experience |
Supports technology projects that add to core competencies and/or reduce costs. Supports successful new product launches as an Operations Team Member. Duties include, but are not limited to, providing input for P/DFMEA, developing robust processes, continuous improvement projects, ensuring accuracy and communication of COGS. | 2/17/2020 |
| 12297 | Smiths Medical Minneapolis, MN Product Surveillance Reporting Specialist I BS/BA Exp: 1-2 year in product complaint handling |
The PSR Specialist I contributes to the strategic management of global adverse event reporting, communications with regulators, and risk management activities through the execution of timely, high quality and consistent processes. This role contributes to the on-going improvement of processes, including appropriate identification and response to risks, adverse event reporting decisions. | 2/17/2020 |
| 12298 | Smiths Medical Dublin, OH Quality Engineer II MS in engineering Exp: 1-3 years |
The Quality Engineer II will support and drive continuous improvements of quality systems and manufacturing processes, including CAPA investigation and solution activities. This role will also help drive quality activities related to continued compliance to changing regulatory requirements. Conducts engineering activities of intermediate scope or degree of difficulty. This could include medium – large components/system, processes associated with a medium or large project.The Quality Engineer II will support and drive continuous improvements of quality systems and manufacturing processes, including CAPA investigation and solution activities. This role will also help drive quality activities related to continued compliance to changing regulatory requirements. Conducts engineering activities of intermediate scope or degree of difficulty. This could include medium – large components/system, processes associated with a medium or large project. | 2/17/2020 |
| 12299 | Smiths Medical Denver, CO Field Support Specialist - Registered Nurse (RN) RN Degree and License Exp: 1-3 years in clinical bedside nursing |
The FSS will work closely with current customers as well as potential customers as the clinical expert on the sales team. The Vascular Access devices provide healthcare professionals access to patients’ vasculature for delivery and withdrawal of fluid and medication, as well as devices to protect health workers by helping prevent needle stick injuries.The FSS will work closely with current customers as well as potential customers as the clinical expert on the sales team. The Vascular Access devices provide healthcare professionals access to patients’ vasculature for delivery and withdrawal of fluid and medication, as well as devices to protect health workers by helping prevent needle stick injuries. | 2/17/2020 |
| 12300 | SomaLogic Boulder, CO Marketing Research Associate, Diagnostic Tests BS/BA or MS Exp: 1-2 years |
The Market Research Associate will work to research and define several markets that SomaLogic might enter. This critical piece of work will include researching product-level competitors and uncovering the alignment between product opportunity and customer needs. Identify competitors for diagnostic products that are currently in the market, in development, or in the pipeline. Clarify and augment proposals for new product development. Develop detailed competitive profiles for new products. | 2/17/2020 |
| 12301 | SonoSite Bothell, WA Manufacturing Associate (2nd shift Transducers, Temporary 12 months) HS Diploma/GED Exp: 0-1 years in high tech manufactruing |
Follow all required procedures such as Assembly Instruction, Personal Protective Equipment, and Device History Record while performing the job responsibilities. Weighing and mixing epoxy-based materials. Cleaning and assembling high precision molds. Light mechanical assembly of small components using hand tools and torque drivers. Work with hands under a microscope performing hand soldering of fine pitch cables and flexible circuits. | 2/17/2020 |
| 12302 | Sorrento San Diego, CA Quality Control Microbiology Associate BS/BA in microbiology Exp: 1-2 years industry experience |
This individual will contribute to providing microbiological support and testing of cGMP environments, as well as contribute to in-process, drug substance, and drug release testing. Environmental monitoring of cGMP cleanrooms per FDA and USP guidelines. Input and manage environmental data. Conduct QC testing of raw materials and utility samples; QC tests include, but not limited to bioburden, endotoxin, total organic carbon, conductivity, osmolality, and pH. | 2/17/2020 |
| 12303 | Sorrento San Diego, CA Research Associate BS in biological sciences Exp: 0-1 years |
The successful candidate will have a major support role for the Chemical Immunotherapy group. Responsible for execution of cell-based assays to support characterization/development of lead candidates. Aid in mechanistic and target validation studies using ELISA, SDS-PAGE, Western Blot, and flow cytometry. Partake in instruments’ maintenance and calibration, lab cleanliness and orderliness, as well as ordering and replenishing stocks | 2/17/2020 |
| 12304 | Sorrento San Diego, CA Research Associate BS in bio/chemistry/nanotechnology Exp: 0 years |
We are currently seeking a Research Associate for the Nanoformulations group. This individual will play a critical role in supporting experiments to identify and evaluate molecules for nanoparticle formulation and drug delivery. They will be responsible for performing routine laboratory analysis and maintenance. We are currently seeking a Research Associate for the Nanoformulations group. This individual will play a critical role in supporting experiments to identify and evaluate molecules for nanoparticle formulation and drug delivery. They will be responsible for performing routine laboratory analysis and maintenance. | 2/17/2020 |
| 12305 | Sorrento San Diego, CA Manufacturing Associate II MS or BS in biological/chemical sciences Exp: 1 year in cGMP manufacturing |
We are currently seeking a Downstream Manufacturing Associate II. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. An essential component of this position will be an understanding of cGMP methodologies: SOP’s, batch record preparation and execution, deviation control and general clean room maintenance. | 2/17/2020 |
| 12306 | Sorrento San Diego, CA Materials Associate HS Diploma/GED Exp: 1-2 years in inventory management |
The Materials Associate's responsibilities are divided into three primary functional areas: shipping and receiving, inventory accountability, and other duties. Create and maintain inventory records and forward to appropriate departments. Issue supplies, materials and equipment to workers and ensure that all corresponding paperwork is accurately managed. Perform physical inventory inspections to ensure 100% of inventory accuracy. | 2/17/2020 |
| 12307 | Sorrento San Diego, CA Manufacturing Associate I BS/BA in biological/chemical sciences Exp: 1 year in manufacturing |
We are currently seeking a Downstream Manufacturing Associate I. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. | 2/17/2020 |
| 12308 | Sorrento San Diego, CA Research Associate II BS or MS in biological sciences Exp: BS: 1-2 years, MS: 0-2 years |
Sorrento Therapeutics’ is seeking an experienced Research Associate who will be responsible for the development and implementation of in vitro functional T cell assays to support pre-clinical validation of CAR-T cellular therapies against cancer. The individual must have knowledge and hands on experience in CAR-T, cell culture, Flow cytometry and T cell biology. | 2/17/2020 |
| 12309 | Spark Therapeutics Philadelphia, PA Research Associate RVC (Assay) BS or MS in biological sciences, chemical sciences/engineering Exp: 1-3 years |
The successful candidate’s primary responsibilities will be to execute and improve established protocols for production, characterization and sequence verification of DNA constructs for pre-clinical grade rAAV vector production. The incumbent will also assist therapeutic area scientists in cloning and synthesis of new DNA constructs to support the translational pipeline and will be the point contact for pasmid banking. | 2/17/2020 |
| 12310 | Philips Fresno, CA MR/CT Field Service Engineer 1 AS/AA in electronics Exp: 1+ years in servicing electronics |
This position will be responsible for customer relationship management through the effective use of technical knowledge to install, troubleshoot, service, and maintain equipment at customer sites; generate service revenue; adherence to state and federal regulatory requirements. This position is an entry level position for an employee with limited experience. | 2/17/2020 |
| 12311 | Spherotech Lake Forest, IL Quality Control Associate BS/BA in chemistry Exp: 1 year |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. This position requires a Bachelor's degree in Chemistry or related field and a minimum of 1 year of experience. | 2/17/2020 |
| 12312 | Sprint Cleveland, OH Sales and Customer Support Associate BS/BA Exp: 0-2 years in sales/customer support role |
Accurate, efficient and timely data management within CRM (Customer Relationship Management) Tool. Order processing and shipment. Provide phone support and coaching to patients, physicians and other internal and external resources. Assists sales team in lead creation and account management. Supports sales team by recording patient procedure and follow-up data | 2/17/2020 |
| 12313 | SRI International Arlington, VA Research Analyst – Science, Technology & Innovation Policy BA or MA in public policy or related Exp: 1-5 years |
A Research Analyst will work across all these areas and will: Implement approaches to projects under the direction of senior staff. Apply a variety of methods to analyze complex issues and to generate findings and recommendations in collaboration with senior staff. Produce pieces of well-written high-quality reports and presentations for clients in collaboration with team members. Occasionally travel domestically and internationally. | 2/17/2020 |
| 12314 | SRI International Princeton, NJ Project & Resource Analyst BS/BA in business/project management/related Exp: 0-2 years |
Plan and maintain detailed integrated master schedule (IMS) combining multiple projects/product lines including design and program milestones, manufacturing development, assembly, test, and into production operations. Assist in laying out and tracking major project milestones, workflow, and activities in relation to schedule and resources and identify gaps and constraints in program performance. Interface with Engineering, Finance and Business Operations, and Program Management to develop program requirements into the IMS baseline. | 2/17/2020 |
| 12315 | SRI International Harrisonburg, VA Bioscience Research Associate - Macromolecular Bioscience BS/BA in biochemistry/biotechnology Exp: 1-5 years |
We are seeking an enthusiastic research associate to work in a multidisciplinary team of biochemists, chemist, and molecular biologist. Perform a variety of laboratory techniques such as peptide synthesis and purification, microscopy, flow cytometry, mammalian cell culture, PCR, mass spectrometry and routine biochemical techniques. Collaborate with scientists from other disciplines (e.g., in chemistry, molecular biology, cancer biology, and immunology) in cross-divisional teams. | 2/17/2020 |
| 12316 | Charles River Mattawan, MI Research Technician - Pharmacokinetics and Acute Toxicology BS/MS Exp: No experience necessary |
We are seeking a Research Technician for our Pharmacokinetics and Acute Toxicology Team at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. Please Note: we are seeking Talent for both 1st and 2nd Shift positions, as well as standard and alternate work schedules (e.g., M-F, Tu-Sat) The following are minimum qualifications related to the Research Technician position: HS/GED or Bachelor’s/Master’s with no relevant experience. etc. | 2/17/2020 |
| 12317 | Charles River Mattawan, MI Research Technician - Neurobehavioral Sciences BS/MS Exp: No experience necessary |
We are seeking a Research Technician for our Neurobehavioral Sciences Team at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. Please Note: we are seeking Talent for both 1st and 2nd Shift positions, as well as standard and alternate work schedules (e.g., M-F, Tu-Sat). etc. | 2/17/2020 |
| 12318 | Charles River Mattawan, MI Research Technician - Developmental and Reproductive Toxicology BS/MS Exp: No experience necessary |
We are seeking a Research Technician for our Developmental and Reproductive Toxicology Team (for both In-Life and the Teratology Laboratory) at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. Please Note: we are seeking Talent for both 1st and 2nd Shift positions, as well as standard and alternate work schedules (e.g., M-F, Tu-Sat). etc. | 2/17/2020 |
| 12319 | Charles River Reno, NV Research Assistant 1 (Laboratory Sciences) BA/BS in a laboratory science or related Exp: 0-2 years |
We are seeking a Research Assistant I for our Safety Assessment site located in Reno, NV. This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. The following are minimum requirements related to the Research Assistant I position. Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required. Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. etc. | 2/17/2020 |
| 12320 | Charles River Shrewsbury, MA Animal Care Technician 1 HS diploma or equivalent Exp: 6+ months |
We are seeking an experienced Animal Care Technician I for our Safety Assessment site located in Shrewsbury, MA. Responsible for performing operational, administrative and technical tasks to provide comprehensive care for all species of laboratory animals at the site, including: daily health observations, feeding/watering, sanitizing primary and secondary enclosures, environmental enrichment, handling and restraint and related tasks. Assist with the movement of animals and stocking of supplies. May serve as lead/primary technician and perform technical duties with guidance. | 2/17/2020 |
| 12321 | Charles River Ashland, OH Research Technician 1 HS diploma/BS Exp: 6-12 months |
We are seeking an experienced Research Technician I for our Safety Assessment site located in Ashland, OH. The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical obsercations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 2/17/2020 |
| 12322 | Charles River Malvern, PA Quality Assurance Auditor 1 BS/BA Exp: 1-2 year(s) |
This position is responsible for performing Quality inspections of routine processes in the Manufacturing department. These inspections may occur in aseptic production rooms. The Auditor I will also be responsible for a Quality review of basic records and reports in support of the Manufacturing department to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures. We are seeking a Quality Assurance Auditor I for our Biologics Testing Solutions site located in Malvern, PA. The following are responsibilities related to the Quality Assurance Auditor I position. Assure Charles River’s compliance with applicable federal, state, and local regulations as well as corporate policies to avoid any business interruptions. Communicate all identified compliance and quality risk to supervisor. etc. | 2/17/2020 |
| 12323 | ChemGenes Wilmington, MA Junior Chemist BS in chemistry Exp: Not necessary for BS candidates |
The job duties: Manufacture of DNA & RNA compounds. Assist Senior Chemists. Prepare test solutions, reagents and ability to carry out reactions, to produce specialized ultra pure DNA/RNA synthesis products. Operate rotary evaporators, chillers, etc. Preform column chromatography: small scale (on the bench) & large scale. Follow SOPs of standard products; report any deviations to Senior Chemists. Communicate with QC & QA department to update/create certificates of analysis. Maintain timely documentation of work. Evaluate data & prepare technical reports. General lab maintenance as necessary. etc. | 2/17/2020 |
| 12324 | CheminPharma Branford, CT Associate Scientist, Medicinal/Synthetic chemistry BS/MS in synthetic chemistry Exp: 0-5 years |
The successful candidate will be an experienced chemist with state of the art knowledge of synthetic organic chemistry and will be a motivated, creative, hands-on laboratory scientist with the ability to interact effectively with team members and external customers. Major responsibilities will involve design, synthesis, purification, and characterization of novel chemical entities and the management of general chemistry lab operations under the direction of senior scientific staff. The qualified individual is expected to contribute to process development and scale-up of key intermediates. | 2/17/2020 |
| 12325 | Clinlogix Chicago, IL Clinical Research Associate BS in a life science Exp: 1-3 year(s) |
The Clinical Research Associate reports to and works under the direction of the Manager, Global Clinical Monitoring. Responsible to monitor clinical trials, study sites and clinical data while ensuring compliance with protocol and overall clinical objectives and Good Clinical Practice (GCP). Provides administrative and project support to clinical programs with minimum supervision. Interfaces with all project/clinical team members and off-site personnel as needed in support of project and departmental goals and responsibilities. etc. | 2/17/2020 |
| 12326 | Codexis Redwood City, CA Research Associate, Process Development-Downstream MS Exp: 1-2 year(s) |
The Process Development Associate will be responsible for the development, optimization, and scale-up of protein purification processes. The ideal candidate will have experience with the optimization of enzyme recovery/purification processes. Responsibilities Include: Perform protein recovery experiments using unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration. Perform resin screening, column chromatography (IEX, HIC, MMC, CHT etc.). Analyze processing samples, using biological, biochemical, and other relevant analytical methods. Communicate results of experiments to the Project team. Participate in daily operation and routine maintenance/housekeeping of process and analytical equipment. etc. | 2/17/2020 |
| 12327 | Colopast Coral Springs, FL Inside Sales Representative (Physician Relationship Manager) HS diploma or equivalent Exp: 1+ year(s) |
Comfort Medical, a wholly owned subsidiary of Coloplast, is seeking an Inside Sales Representative to join our team in our Coral Springs office. You will build your own sales relationships/accounts, resolve customer questions, and offer solutions to drive company revenue. Your primary call points will include Physicians' and healthcare providers' offices. Comfort Medical preferred manufacturers, and customers. This role is heavily phone-based. Responsibilities: Present and sell company services to new and existing customers. Prospect and contact potential customers. Achieve agreed upon sales targets by the deadline. etc. | 2/17/2020 |
| 12328 | Concerto King of Prussia, PA Pharmaceutical Data Analyst – Analytics BA/BS in a laboratory science or related Exp: 1-4 year(s) |
ProMetrics, a Concerto HealthAI company, is seeking a highly proficient Data Analyst who will thrive in our agile, fast-paced, and delivery-focused environment. As an integral part of the analytics team, the data you analyze will provide valuable insight to our clients, who happen to be some of the most influential brands in the pharmaceutical industry. You’ll be responsible for understanding system requirements, documentation, verifying, and testing data integrity and quality being displayed on ProMetrics’ proprietary systems. Most importantly, you’ll be accountable for delivering client data in an accurate and timely fashion. etc. | 2/17/2020 |
| 12329 | Conformis Wilmington, MA CAD Engineer I BS in engineering or equivalent Exp: 1-2 year(s) |
The CAD Engineer I will be responsible for designing and reviewing patient-specific implants and surgical instruments using various software packages while ensuring Conformis quality standards. Essential Duties and Responsibilities: Develop and maintain strong internal working relationships across Conformis. Understand the objectives, responsibilities, and mission of the CAD department and works towards those goals. Prioritize and plan work activities; adapt for changing conditions. Generate 3D models from diagnostic CT images and use commercial and research software to design patient specific implants and surgical instruments. Work independently to achieve departmental and personal goals. Plan and manage workload effectively and efficiently. etc. | 2/17/2020 |
| 12330 | Conformis Billerica, MA Finishing Technician I, 2nd Shift HS diploma or equivalent Exp: 1-3 year(s) |
This position is responsible for operation of post-machining finishing of medical implants in a high-volume manufacturing environment. 2nd Shift – Mon – Fri, 3:00pm – 11:30pm. Essential Duties and Responsibilities: Develop and maintain strong internal working relationships across Conformis. Understand the objectives, responsibilities, and mission of the Production Department and work towards those goals. Understand assigned quality and delivery targets, and consistently meet or exceed expectations. Prioritize and plan work activities; adapt for changing conditions. Perform blasting, hand-finishing, and polishing of metal medical implants post CNC machining. etc. | 2/17/2020 |
| 12331 | Contract Pharmacal Corp Hauppage, NY Scientist I; AR&D BS/MS in chemistry or analytical chemistry Exp: 1-2 year(s) |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. Responsibilities: Responsibilities include, but are not limited to: Knowledge of USP and FDA requirements. Design and conduct full analysis of Dietary Supplements and Active Pharmaceutical Ingredients (API) products and their impurities. Conduct assay, content uniformity, dissolution, in-process blend, and blend uniformity of newly developed and stability samples in support of formulation and process development. Prepare result documentation for department and general review. etc. | 2/17/2020 |
| 12332 | Contract Pharmacal Corp Hauppage, NY QA Manufacturing, Specialist AAS/BA/BS Exp: 1 year |
The QA Manufacturing Specialist has primary responsibility for handling all front office operations as outlined below. Responsibilities: Including but not limited to: Ensure that the daily batch request list, provided by Materials Management, conveys to accurate and on-time issuance of production and non-commercial batches. Request issuance of batches with related labels (bulk and IP). Updating production board accordingly. Consolidate information regarding batches on production data roster spreadsheet used by Manufacturing Operations, Account Services, and Materials Management. Maintain weekly & quarterly reporting of current production of materials processing and finished production. etc. | 2/17/2020 |
| 12333 | Contract Pharmacal Corp Hauppage, NY Chemist I; QC Finished Product & Validation BS in chemistry Exp: 1+ year(s) |
A Chemist Level I is responsible for performing chemical testing and completion of real-time documentation per cGMPs and current SOPs. Essential Job Functions: Perform UPLC, HPLC, GC, UV-vis, FTIR, ICP, TOC and wet chemistry testing. Proficient in various UPLC and HPLC software programs, such as Empower and EZ-Chrom. Assist in writing SOPs and Test Procedures following good documentation practice per company's SOP and cGMP regulations. Assist in OOS investigations. etc. | 2/17/2020 |
| 12334 | Corvus Pharmaceuticals Bulingame, CA Animal Technician/Lab Assistant AS/BS in biology or related Exp: 0-2 years |
Role and Responsibilities: Performs the general husbandry of research animals for experimental purposes. Performs animal welfare checks. Performs cell inoculations via multiple routes (SC, tail vein, RO). Performs dosing via multiple routes (IV, PO, SC, IM). Performs necropsy/tissue sample collection for evaluating PD endpoints. Performs bleeding via multiple techniques (RO, cardiac punch, cheek) for evaluating drug PK. Performs various vivarium cleaning duties. etc. | 2/17/2020 |
| 12335 | Covance San Carlos, CA Study Technician Animal Operations-Metabolic Studies BS in the life sciences Exp: Entry level |
In this position your work will have a real life positive impact of improving health around the world. Upcoming or recent graduates in Animal Science, Biology and related life sciences field encourage to apply. Veterinary Technicians looking to to work in research setting are encouraged to apply. In this role you'll be working with Scientist performing study task with small animal models. Extensive training is provided for this entry level Study Tech position. Duties include but not limited to: Monitoring of animal health and welfare in compliance with the Animal Welfare Act, determines and documents clinical observations, body weight data, and food consumption data. Prepares Dose Formulations, buffer solutions and control substances. etc. | 2/17/2020 |
| 12336 | Covance Madison, WI Research Assistant (I) - Immunotoxicology BS/BA in a related scientific field Exp: 1-2 year(s) |
We have a great opportunity for a Research Assistant (I) - Immunotoxicology in our Immunology and Immunotoxicology (InI) Group in Madison, WI. Covance’s work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life-saving work and help improve patients' lives while growing your career. In this role, you will set up and prepare equipment for sample processing, data acquisition/analysis according to study protocol, Policies/SOPs, Methods, and regulatory guidelines. You will also be responsible for performing assays, maintenance, and general laboratory support duties. Organizes and conducts routine and non-routine processing in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines. Documents work and maintains study documentation and laboratory records. etc. | 2/17/2020 |
| 12337 | Covance Greenfield, IN Sampling Handling I Assistant HS diploma or equivalent Exp: Entry level |
In this role it’s a unique combination of sample management and archive tasks, including labeling, receipt, transferring, tracking, inventory, archival, shipping, and disposal of samples and/or materials. Samples include paper data, wet tissues, slides, blocks and frozen biological samples. Excellent keyboarding skills required as this position will have a high degree of data input into tracking and archive database, may involve repeated lifting of up to 50 lbs. Excellent customer service skills are required as position interfaces with internal and external customers in retrieving and storage of samples all while maintaining strict business confidentially. etc. | 2/17/2020 |
| 12338 | Covance Salt Lake City, UT Sample Handling Assistant HS diploma or equivalent Exp: Not required |
Job Overview: Performs any combination of sample management and/or archive tasks, including labeling, receipt, transferring, tracking, inventory, archival, shipping, and disposal of samples and/or materials. Sample accession core tasks, including box opening, inventory/labeling, receipt/store, and pulls/returns. Uses tracking systems as appropriate to maintain sample and study integrity. Accurate protocol and relevant documentation interpretation (i.e., Sample Analysis Outline, client paperwork). Document and communicate discrepancies to appropriate personnel, and assists with problem solving. etc. | 2/17/2020 |
| 12339 | Covance Princeton, NJ Associate I Regulatory Submissions BS in a life science Exp: 0-1 year(s) |
Covance is seeking candidates for an Associate I Regulatory Submissions. The Associate I Regulatory Submissions is an office based role in Princeton, NJ. Assist in the preparation of submissions filed to Regulatory Authorities (e.g.: INDs, CTAs, NDAs, NDSs, MAAs or CTDs). Contribute to the preparation of submissions to Regulatory Authorities by reviewing/summarizing scientific/research documents. Assist in the coordination, collection and organization of information required by Regulatory Authorities. Interact with the Publishing group, Copy Center or equivalent as necessary for the production of submissions. etc. | 2/17/2020 |
| 12340 | Covance Denver, PA Animal Tech I (3rd Shift) HS diploma or equivalent Exp: Not required |
As an Animal Care Technician in our Immunology Services you'll have a connection to the life improving changes we make at Covance. In this position you’ll work closely with a variety of laboratory animals in barrier housing Extensive training provided! Responsibilities include but not limited to; Responsible for monitoring and maintaining the physical environment conditions of the animals in research setting. Comply with appropriate safety and health practices including personal protective equipment and barrier requirements, as applicable. Perform animal husbandry (clean, feed, sanitation, enrichment, etc.) on a regular basis. Perform and document daily observations of animal health status. etc. | 2/17/2020 |
| 12341 | Covance Greenfield, IN Material Controller Tech I HS diploma Exp: 0-3 years |
Purchasing: Process purchase and material requisitions for the Facility Management Department. Coordinate and expedite stock and non-stock material requisitions for maintenance repair. Work closely with Facilities planners/schedulers, maintenance supervisors, and crafts persons to coordinate delivery schedules, provide purchase order information and resolve invoice discrepancies. Perform RCP duties as delegated. etc. | 2/17/2020 |
| 12342 | Myriad Bioscience South San Francisco, CA Client Services Associate BA/BS Exp: 1-3+ year(s) |
The Client Services Associate will be on the front lines and will act as the face of the organization for our customers including physicians, clinics, medical staff, and patients. We handle a variety of complex inbound and outbound inquiries to assist and empathize with our customers, some who may be experiencing stress. We work to resolve and preempt customer issues to ensure a positive customer experience. Myriad Women’s Health Client Services team provides a differentiated customer experience because we hire amazing people to join this team. Our Client Services Associates are highly skilled, motivated people who are driven by human interactions and solving problems. etc. | 2/17/2020 |
| 12343 | Crinetics San Diego, CA Research Associate, Drug Metabolism and Pharmacokinetics BA/BS/MS in a relevant scientific field Exp: 1-2 year(s) |
Crinetics Pharmaceuticals is seeking a Research Associate (RA) or Senior Research Associate (SRA) to join its growing and dynamic development team. This individual will be responsible for performing a variety of DMPK and bioanalytical assays. The work will support projects at various stages drug discovery and development thereby allowing the selected candidate to play an active role in our drug discovery and development efforts to advance small molecule therapeutics for rare endocrine disorders and endocrine-related cancers. This is a unique opportunity to work with a proven and well-funded drug discovery and development team in a small company environment in the heart of San Diego’s biotechnology community. (Position will be filled at level commensurate with experience) etc. | 2/17/2020 |
| 12344 | CRISPR Therapeutics Cambridge, MA Research Assistant -II: QC Data Review MS Exp: 1-2 year(s) |
Job Summary: Support CMC Analytical activities for Crispr clinical programs by reviewing batch records, assay results. Perform Data Review for integrity and accuracy and collate data in a highly organized manner. Use statistical software to analyze the data for shelf life trending and control chart trending. Monitor stability program for time pulling of the samples, scheduling and following the results with the testing labs. This is a Cross-functional and highly visible position within Technical Operations group. The position requires active collaboration with research, process development and quality teams and CDMOs. etc. | 2/17/2020 |
| 12345 | CSBio Menlo Park, CA Chemist, Quality Control MA/MS in chemistry, biochemistry, or biology Exp: Recent graduates |
We are seeking a qualified individuals to join us as Quality Control Chemists at our Menlo Park facility. This position will be responsible for conducting QC testing for release, stability, and raw materials, as well as executing experiments in support of routine QC testing utilizing various analytical techniques. Core duties and responsibilities include the following: Conduct sample analysis using various analytical techniques, including HPLC, UPLC, GC, KF, FT-IR, TLC, and LC-MS, GC-MS. Preparation of laboratory reagents and samples; operation of instruments; data analysis; preparation of analytical reports; notebook documentation. etc. | 2/17/2020 |
| 12346 | CSL Behring Gresham, OR Plasma Processing Technician HS diploma or equivalent Exp: 3+ months |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. 1 In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2 Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3 May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4 Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. etc. | 2/17/2020 |
| 12347 | CSL Behring Cheektowaga, NY Plasma Processing Technician HS diploma or equivalent Exp: 3+ months |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. 1 In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2 Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3 May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4 Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. etc. | 2/17/2020 |
| 12348 | CTI Chicago, IL Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 12349 | CTI Dallas, TX Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 12350 | CTI Cincinnati, KY Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 12351 | CTI Philadelphia, PA Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 12352 | CTI Raleigh, NC Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 12353 | CTI San Francisco, CA Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 12354 | CTK Biotech Poway, CA Production Assistant AS/BS Exp: 0-3 years |
The Production Assistant is mainly responsible for manufacturing biological products following SOP and maintaining production related records. Essential Duties and Responsibilities: Production of Recombinant proteins, monoclonal antibodies, and other biologics per work instruction. Conducting general lab maintenance, including glass washing, buffer/reagent preparation, proper disposal of waste, and inventory organization. etc. | 2/17/2020 |
| 12355 | CTK Biotech Poway, CA Production Associate MS Exp: 1+ year(s) |
The Production Associate is mainly responsible for manufacturing biological products following SOP, maintaining production records and generating production document. Essential Duties and Responsibilities: Produce qualified antigens, antibodies, and other biologics per work instruction. Conducting general lab maintenance, including glass washing, buffer/reagent preparation, proper disposal of waste, and inventory organization. Communicating constantly with team members and related departments. etc. | 2/17/2020 |
| 12356 | Semma Therapeutics Cambridge, MA Quality Control Associate MS in pharma/biotechnology Exp: 1 year |
This position will perform QC tests for pre-clinical and clinical material from specific manufacturing steps associated with ES derived pancreatic islet production, from cell bank thaw through fil/finish. QC testing will include stability test for cell banks and final product, in-process manufacturing tests and final product lot release tests. The candidate will be expected to assume additional QC testing responsibilities associated with specific projects | 2/16/2020 |
| 12357 | Semma Therapeutics Cambridge, MA GMP Manufacturing Associate, Clinical Materials BS/BA in biological/bioengineering/chemical engineering Exp: 6 months in process development/manufacturing |
Perform product manufacturing for clinical materials according to cGMP standards. Includes assembling raw materials, following specific standard operating procedures (SOP), aseptic technique, completing batch records, reporting deviations. Participates and facilitates technology transfer and final process development from the Research to the Manufacturing group. Assists in the development of Standard Operating Procedures (SOPs) for manufacturing in collaboration with Research and Quality Systems groups | 2/16/2020 |
| 12358 | LabCorp Overland Park, KS Data Entry Operator/Lab Data Entry HS Diploma/GED Exp: 1-3 years |
Operates various data entry terminals and automated data systems to record and verify billing/accounts receivable information, customer demographic data and laboratory data identification and results, for computer processing. Resolves suspend and billing problems and manually process OE batches. Follows standard sequences and coding in entering and/or keying in data in correcting, editing, and verifying all data entered into automated systems. | 2/16/2020 |
| 12359 | LabCorp RTP, NC Molecular Oncology Tech Trainee/Technologist (1st Shift) BS/BA in biology/chemistry Exp: 1 year in clinical OR research lab |
Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation. Demonstrate the ability to make technical decisions regarding testing and problem solving. | 2/16/2020 |
| 12360 | LabCorp Dublin, OH Medical Technologist - Virology BS/BA in biology/chemistry/med tech/etc. Exp: 1 year in clinical lab experience |
This position will work within the Virology section of the microbiology department.Testing performed will include Virology testing, IFOBT, H.Pylori breath bag testing and cepheid testing. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. | 2/16/2020 |
| 12361 | LabCorp Shelton, CT Laboratory Technologist Trainee - Histology BS/BA in biology or chemistry Exp: 1 year in research lab |
Perform all technical grossing procedures required to process and submit specimens for microscopic review as per standard operating procedures under the indirect and direct supervision of pathologists. Operate and maintain automated tissue processors, perform tissue embedding, Cryostat sectioning, operate and maintain tissue embedding units. Operate and maintain H&E stainers, IHC stainers, special stains stainers and coverslipping units, perform manual coverslipping | 2/16/2020 |
| 12362 | LabCorp Shelton, CT Cytotechnologist-First Shift BS Exp: 1 year of training in cryotechnology |
Screens and evaluates gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions. Maintains absolute integrity in the accurate performance and reporting of results. Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA and laboratory guidelines | 2/16/2020 |
| 12363 | LabCorp McHenry, IL Phlebotomist HS Diploma/GED Exp: Phlebotomy accredidation |
Perform blood collections by venipuncture and capillary techniques. Prepare all collected specimens for testing and analysis. Order entry of patient and specimen information . Provide superior customer service to all patients and client providers and staff | 2/16/2020 |
| 12364 | LabCorp Burington, NC Specimen Processing Specialist (1st Shift) HS Diploma/GED Exp: 1-3 years in clinical lab |
This position will have first shift hours with the following schedule: 9:00am-5:30am Tuesday to Saturday. This is a multi-discipline role with 3 primary components: specimen accessioning, sample splitting/sorting and data entry. Prepares laboratory specimens for designated departments/locations prior to laboratory analysis and testing and routes specimens by type to various staging areas. Assigns specific computer generated identification numbers, checks for accuracy and records all items processed. Performs all paperwork, technical and non-technical procedures required to process and submit specimens. | 2/16/2020 |
| 12365 | Sera Care Milford, MA Research Associate I BS/BA in biochemistry/molecular biology or related Exp: 1 year in a lab |
Product formulations following production batch records or written instructions. Perform general molecular techniques such as cloning, plasmid purification, gel-electrophoresis, RNA transcription, and bacterial culturing. Perform nucleic acid analyses (RNA/DNA integrity analysis, real time qPCR, digital PCR) and analyze results. Maintenance of different cell lines in Cell culture (viral or bacterial) and manufacture of cell based products as required. | 2/16/2020 |
| 12366 | Seres Therapeutics Cambridge, MA Donation Operations Technician BS Exp: 1-2 years |
The Donation Operations technician is responsible for inventory receipt and management, movement and tracking in accordance with GMP guidelines and Seres policies. The technician is responsible for laboratory assays to examine and characterize donor microbiomes. This position will assist in and/or lead deviations and corrective action plans as they relate to core responsibilities as needed, and perform project based work for program improvement and growth. Some cross functional work may be required. | 2/16/2020 |
| 12367 | Simbex Lebanon, NH Systems Engineer BS in mechanical/electrical engineering or related Exp: 0-3 years in testing products |
The Systems Engineer will be responsible for supporting every phase of the product development life cycle process in order to deliver high-quality products in the consumer and medical device markets. The Systems Engineer will work with the electrical, software, mechanical, product technical support, and quality teams to help develop, integrate, and test sub-assemblies into product. The ideal candidate has broad skills but deep knowledge/skills in one area, and is able to blend human-centric design with sound engineering principles across a wide range of engineering domains with a focus on quality and willingness to wear many hats. | 2/16/2020 |
| 12368 | Seven Bridges Boston, MA IT Help Desk Analyst BS/BA Exp: 1+ years in helpdesk, IT, secruity, technolopgy |
The successful candidate will bring expertise in IT Laptop Support, IT Procurement, Troubleshooting Laptop and Software Issues, Networking, Facilities, IT Tooling and Implementation. The successful candidate must excel at providing excellent support to Seven Bridges employees in a fast paced environment. This role requires the right blend of technical and non-technical skills, and will be working across the Seven Bridges global organization. | 2/16/2020 |
| 12369 | Shionogi Inc Florham Park, NJ Contract -- Regulatory Documentation Specialist HS Diploma required, BS/BA preferred Exp: Entry Level |
The Regulatory Documentation Specialist is responsible for supporting the Regulatory Affairs Submission Team with the preparation of regulatory documents for both eCTD (electronic common technical document), as well as traditional paper submissions. The scope of this role includes assisting in the document remediation and formatting of documentation for submissions to Health Authorities. The ideal candidate for this entry level position is enthusiastic, highly organized and flexible. | 2/16/2020 |
| 12370 | Siemens Chicago, IL Power Monitoring Solution Engineer (Entry Level) BS in electrical engineering or computer informations systems Exp: Entry Level |
Siemens is looking for a Solution Engineer to join their growing team. The candidate will be responsible for the integration of hardware and software to create an overall energy monitoring system for customers. Digital Solutions & Services provides facilities with the tools which help in managing the energy costs and availability of their business. | 2/16/2020 |
| 12371 | Siemens Hoffman Estates, IL Materials Support I HS Diploma/GED Exp: Entry Level |
This role will be responsible for the picking of production orders and placement of inbound materials. You will also be responsible for deliveries of materials to manufacturing. In addition, you will be required to have an active role in cycle counting inventory. You should be able to handle cross functional duties (ie Shipping, Receiving) within the area. | 2/16/2020 |
| 12372 | Siemens Irving, TX Security Technician I - Service HS Diploma/GED Exp: 0-1 year in maintenance |
Coordinates with contractors in the process of servicing of systems sold by a branch office. Monitors and controls serviceability progress based on project schedules and milestones to deliverable timelines. Performs system commissioning on systems including loading software programs and implementing modifications as necessary | 2/16/2020 |
| 12373 | Siemens Newkirk, OK Wind Service Technician HVAC/electrical/aviation field certification Exp: 1 year of wind technician experience |
The Field Service Technician must perform scheduled maintenance, troubleshooting, part replacement, and retrofits as necessary to maintain quality and availability for our customer. Must maintain safety and professionalism and keep accurate and detailed records of parts used and work performed | 2/16/2020 |
| 12374 | Signant Health Blue Bell, PA Application Specialist BS/BA in comp sciences Exp: 1-3 years in SQL knowledge |
Perform requirements gathering and business analyst tasks for eCOA collection, reporting and data transfer. Provide guidance to the client on the most suitable solution, ensuring that all recommendations are achievable within the scope of the product. Develop eCOA solutions using proprietary TrialMax platform (Web, Slate, Touch) according to the requirements gathered and interpretation of the client clinical protocol. Present eCOA solutions at client design review and testing (UAT) meetings at customer sites (as required) | 2/16/2020 |
| 12375 | Sigvaris Group Peachtree City, GA Technician 2 year degree/cert in mechanical/industrial/electrical field Exp: 1-3 years on circular knitting machines |
This position is responsible for the general repair of hosiery knitting machines to ensure first quality products are produced to company specifications. Performs required/needed maintenance knitting machines to ensure machines are operating in good working order. Addresses machine stops to keep machines operating efficiently. Performs preventative maintenance as outlined in weekly PM sheets. | 2/16/2020 |
| 12376 | Sinclair Research Auxvasse, MO Report Coordinator/Technical Writer BS/BA in sciences Exp: 1 year experience |
You will be writing GLP and non-GLP reports for all research studies performed. It is your responsibility to ensure written reports meet or exceed standards for formatting, clarity, accuracy, and completeness. Reviewing data, preparing summary tables, and reviewing protocol will fill your day when you are not consulting with study personnel. Accuracy and timeliness is a must in this role. | 2/16/2020 |
| 12377 | Sinclair Research Auxvasse, MO Animal Technician HS Diploma/GED Exp: 0 years |
The ideal candidate will be hard-working and ready to be hands on. In this role, you will have a chance to participate daily in our research by working closely with our study directors, senior technicians, and scientists in order to conduct studies. Animal Technicians begin by learning the basics of data collection and animal husbandry and have the chance to move up into high level Technician roles. | 2/16/2020 |
| 12378 | Sinclair Research Auxvasse, MO Swine Production Technician HS Diploma/GED Exp: 1 year experience |
Sinclair Bio Resources is a unique swine production facility dedicated to producing the highest quality animal models for research facilities around the country. Your day will be spent taking care of these future heroes in medicine. Feeding, grooming, sanitation, animal health, you'll do it all! There is room for advancement and specializing in husbandry, breeding, and sample collection. Someone dedicated to animal welfare and eager to make a difference in the lives of others will excel at SBR! | 2/16/2020 |
| 12379 | Sinclair Research Auxvasse, MO Animal Caretaker HS Diploma/GED Exp: 0 years |
The ideal candidate will have a passion for animal welfare and a great work ethic. Hard-working individuals looking for a great environment and a chance to make a difference will fit right in. Your primary role will be taking care of our animals and sanitizing their housing and our buildings. | 2/16/2020 |
| 12380 | Sinota Solutions Bloomington, IN Singota Solutions HS Diploma/GED Exp: 0-1 years in life sciences/supply chain |
Must be very customer focused to both internal employees and external clients. Must be able to work within the FDA regulated environment per its specific requirements and those established by internal policy and standard operating procedures. Computer experience necessary or willing to take internal courses to gain such information quickly.Ability to work with Microsoft Office (Outlook, Excel, Word) a plus. Experience using ERP or inventory systems is not required, but helpful. | 2/16/2020 |
| 12381 | Sinota Solutions Bloomington, IN Associate Quality Control Analyst BS in chemistry Exp: 1 year in formulations/testing/etc. |
Supportthe Quality Control function with respect to raw material, in-process, release and stability testing. Collaboratively participates in Development functionsfor the company including pre-formulation, formulation, process and analytical development activities. Operate various lab instruments and equipment including (but not limited to): Karl Fisher, pH, HPLC, FTIR, UV-VIS, DSC, TOC, Lab-ware washers, Autoclave, Laminar Flow Hoods, Bio-Hazard Hood, Microbalances, and other diverse lab equipment and various wet chemistry techniques | 2/16/2020 |
| 12382 | Sinopia Biosciences San Diego, CA Computational Biologist/Data Scientist MS in bioinformatics/computational biology/comp sci, etc Exp: 0-3 years |
This individual will play a key scientific role in expanding Sinopia’s computational platform and aiding in designing the implementation of follow-up validation studies. They will leverage new computational strategies and disparate data types to discover novel interventions for unmet medical needs. | 2/16/2020 |
| 12383 | Bruker Kennewick, WA Shipping and Receiving Associate HS diploma Exp: 1-2 year(s) |
Responsibilities: Verifies and keeps records on incoming and outgoing shipments and prepares items for shipment. Provide Quality Assurance checks prior to packaging instruments: configuration confirmation and labeling. Cleans, labels, and packages instruments into customer facing final package. Confirms packaged items to ‘pick list’. Determines method of shipment, utilizing knowledge of shipping procedures, routes and rates under direction of Shipping Department lead. Affix shipping labels on packed cartons. Assembles cardboard containers. Inserts items into containers, using spacers, fillers and protective padding. etc. | 2/12/2020 |
| 12384 | C4 Therapeutics Watertown, MA Research Associate, Target Biology BS in biology or related Exp: 1-5 year(s) |
C4 Therapeutics is seeking an enthusiastic, scientifically motivated Research Associate to join our Target Biology team. This candidate will play a significant role in the implementation of in vitro studies to characterize and differentiate the biological consequences of our small molecule therapeutics to advance drug discovery programs. The ideal candidate will possess a background in biology and experience in a research laboratory setting. In addition, the successful candidate will have a strong commitment to team success, ability work effectively as part of a team, and the ability to work on multiple projects simultaneously. This position seeks individuals who are comfortable in a fast-paced environment and interested/committed to laboratory-based research. etc. | 2/12/2020 |
| 12385 | Cardiovascular Systems Pearland, TX Assembly Technician HS diploma or equivalent Exp: 1 year |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. etc. | 2/12/2020 |
| 12386 | Cardiovascular Systems St. Paul, MN Assembly Technician HS diploma or equivalent Exp: 1 year |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. etc. | 2/12/2020 |
| 12387 | CRISPR Therapeutics Cambridge, MA Research Associate, Analytical Development BS/MS in life sciences Exp: 1+ year(s) |
We are seeking a Research Associate to join an exciting, fast-growing and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. etc. | 2/12/2020 |
| 12388 | Celgene Seattle, WA Associate Scientist, Process Analytical Technologies Development MS in biology, immunology, biological engineering or related Exp: 1-3 year(s) |
We are seeking a highly capable and enthusiastic Associate Scientist to work with a multidisciplinary group of engineers and scientists to support the development of novel Process Analytical Technologies (PAT). The Associate Scientist will be responsible for independently executing microscopy-based and cell selection experimentation. The candidate will additionally be expected to execute T cell culture experiments using a combination of scale-down models and manufacturing scale bioreactors. The successful candidate will: Work within a multi-disciplinary environment towards novel applications of Process Analytical Technologies. Independently design experiments, analyze data and draft technical reports to communicate key conclusions. Independently execute multi-parametric cell sorting and flow cytometry experiments. etc. | 2/12/2020 |
| 12389 | Celgene Warren, MI Associate Bioengineer II BS in chemical or biomedical engineering or biology Exp: 0-2 year(s) |
Conducts core MSAT activities in technical transfer, lifecycle management, or validation to support cellular product commercialization. Responsible for technical deliverables, including authoring protocols and reports, with moderate supervision and feedback. Organizes, reviews, and maintains data while developing subject matter expertise. Responsibilities will include, but are not limited to, the following: With supervision, design and execute studies in one of the following areas: technical transfer, lifecycle management, or validation. Perform data analysis, and summarize empirical results, with moderate technical/scientific supervision and feedback. Present results within project team and departmental technical reviews. Conduct Facility Fit studies and work with partner organizations to implement risk mitigations. etc. | 2/12/2020 |
| 12390 | Cell Signaling Technology Danvers, MA Research Associate I BS in a relevant science Exp: 1 year |
We are seeking a highly organized and enthusiastic Research Associate to join our Conjugation team. The successful candiate will assist the team with releasing new products, supporting existing products and providing technical support for all conjugated antibody product lines. Responsibilities: Performs experiments focused on conjugation including dye conjugation, bead conjugation, HRP conjugation, biotin conjugation, PE conjugation and PE tandem dyes for the purpose of enabling the release of direct conjugated antibody products and maintain existing product lines. Performs protein purification and determination. etc. | 2/12/2020 |
| 12391 | Cell Signaling Technology Beverly, MA Product Supply Specialist BS/BA in business, supply chain operations, or a related field Exp: 1-2 year(s) |
We are seeking a Product Supply Specialist to join our Product Supply Team. The role of the Product Supply team is to link the suppliers of our products with our broader Global Supply Chain team, and ensure finished goods inventory is ready and available for customers. Responsibilities: Serve as Supply Chain stakeholder on diverse cross-functional new product introduction (NPI) teams. Serve as key point of contact with vendors for sourced (OEM) products and product packaging materials. etc. | 2/12/2020 |
| 12392 | Cellular Technology Limited Cleveland, OH Laboratory Assistant (Contract Research Laboratory) BS Exp: 1 year |
We are seeking a Laboratory Assistant for our Contract Research Laboratory who will perform immunology testing of client specimens collected from both pre-clinical and clinical studies using the following test methods: ELISPOT, ELISA, flow cytometry, etc. You will help support our quality improvement projects in conjunction with QA, support our quality system by data quality control, communicate with fellow laboratory personnel, maintain laboratory equipment, write reports, etc. All work is performed according to general laboratory safety standards, internal standard operating procedures (SOPs), client protocols, and applicable international, federal and state regulations. | 2/12/2020 |
| 12393 | CEL-SCI Elkridge, MD Assistant Immunologist I BS/BA Exp: 0-2 year(s) |
The Assistant/Associate Immunologist will assist in the day-to-day activities related to the QC testing of Leukocyte Interleukin, Injection (LI) under current Good Manufacturing Practices (cGMP) for clinical application, and QC equipment/facilities operations and maintenance. Specific experience should include: ELISA testing, ELISA assay development, aseptic technique, GMP, analytical chemistry experience, laboratory record-keeping. Skills / Abilities: Quality Control testing of all GMP Manufacturing samples (ELISA, pH, visual inspection). Adhere to written procedures and proper documentation, etc. | 2/12/2020 |
| 12394 | CEL-SCI Elkridge, MD Manufacturing Support Technician AA/AS Exp: 1+ year(s) |
The Support Technician contributes to the manufacturing team effort by accomplishing related tasks and assignments. The Manufacturing Support Technician reports directly to Supervisor of Manufacturing. Responsibilities include, but are not limited to: Use of the autoclave, depyrogenation oven and sonicator. Clean Formulation and Fill Vessels. Gowning for classified areas. Stock and stage processing areas. Other duties as assigned. etc. | 2/12/2020 |
| 12395 | Celsee Ann Arbor, MI Laboratory Research Technician BS in biology or biochemistry Exp: 1-2 year(s) |
The Laboratory Research Technician will work under the guided supervision of an interdisciplinary team of biologists and engineers to validate molecular assays on single-cells. The job responsibilities include: Performing various standard laboratory assays including NGS, Library Prep, PCR, Cell capture and analysis on Celsee’s proprietary devices. Working in sterile conditions to conduct cell culture experiments and maintain the growth of cell lines. Collecting and analyzing generated data. Assisting in organization and upkeep of laboratory supplies, workspace, and equipment. etc. | 2/12/2020 |
| 12396 | Centrillion Hillsboro, OR Laboratory Technician BS/MS in molecular biology, chemistry, data science or other relevant field. Exp: 1-2 year(s) |
MVL is seeking Laboratory Technician for their research and development teams. These positions are in a fast-paced, start-up environment, interacting with R&D scientists from a variety of backgrounds, with a heavy focus on molecular biology and biochemistry. Lab technician will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. The selected individuals will be working in a support role toward the development of new genomics technologies. The candidate will work with multiple scientists to assist with a broad range of duties including making buffers, following protocols, developing or adapting new protocols for new needs. etc. | 2/12/2020 |
| 12397 | Centrillion Palo Alto, CA Laboratory Technician BA/BS in molecular biology, chemistry, genetics, or microbiology Exp: 1-2 year(s) |
Centrillion is seeking Laboratory Technicians for their research and development teams. These positions are in a fast-paced, start-up environment, interacting with R&D scientists from a variety of backgrounds, with a heavy focus on molecular biology and biochemistry. Lab technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. The selected individuals will be working in a support role toward the development of new genomics technologies. The candidate will work with multiple scientists to assist with a broad range of duties including making buffers, following protocols, developing or adapting new protocols for new needs. etc. | 2/12/2020 |
| 12398 | Ceva Lenexa, KS Environmental Monitoring Technician I BS in microbiology, veterinary science, or equivalent Exp: Entry level |
The Environmental Monitoring Technician I will perform microbiological testing involving environmental monitoring, water, and other production utilities to help ensure quality production. The technician will ensure products are tested in a manner consistent with Standard Operating Procedures and in compliance with regulations according to 9CFR. Responsibilities and Key Duties: Perform routine daily, weekly and monthly environmental monitoring testing on processes, utilities, and personnel. Sample purified water system, clean steam, and other utilities for subsequent analysis. Perform assigned sampling tasks carefully and on schedule according to standard operating procedure and supervisor instruction. etc. | 2/12/2020 |
| 12399 | Ceva Lenexa, KS Industrial Development Technician I BA/BS in biology, chemistry, pharmacology, or equivalent Exp: 0-2 year(s) |
Assist in the industrial development, process, and product improvement of viral, bacterial, parasitic and/or recombinant vaccines of licensed and unlicensed vaccines. Responsibilities and Key Duties: GID main responsibilities (including poultry, swine, bovine vaccine viruses and bacteria). Within the assigned internal site, is in charge of the manufacturing and/or analytical testing of development and first commercial batches with a yearly vision. Executes the manufacturing & testing according to the industrial development and process transfer rational (including technical, financial, and regulatory aspects) to anticipate industrial needs - may propose process validation strategy. etc. | 2/12/2020 |
| 12400 | Champions Oncology Rockville, MD Veterinary Technician, Veterinary Services BS in biology, pharmacology, or related Exp: 1+ year(s) |
PRIMARY OBJECTIVES: Support in vivo oncology studies in mice as a member of the Veterinary Services Team. DUTIES AND RESPONSIBILITIES: Conduct daily and weekly assessments and treatments of animals identified with abnormalities. Support the training program by conducting didactic and hands on training courses. Administer the health surveillance program as described, including animal and sample submission and tracking of results. Proficiently perform survival animal surgeries and provide perioperative care. etc. | 2/12/2020 |
| 12401 | Champions Oncology Rockville, MD Research Technician I, Study Services BS/MS in biology, pharmacology, or related Exp: 1+ year(s) |
PRIMARY OBJECTIVES: Support in vivo oncology studies in mice as a member of the Study Services Team. DUTIES AND RESPONSIBILITIES: Perform in-life technical procedures, handle, restrain, and provide care for all animals. Observe animals for general health and overall well-being. Administer therapeutic agents by various routes. Provide animal welfare assessments, including body weight and tumor volume measurement. Allocate animals to study and non-study groups. Provide preoperative animal care. Euthanize animals as directed in study protocols and directives. Under supervision, may act as lead/primary technician on studies. etc. | 2/12/2020 |
| 12402 | Biotronik Lake Oswego, OR Master Data Analyst BS/BA Exp: 1-3 year(s) |
BIOTRONIK is looking to add a Master Data Analyst to our Finance and Sales Operations team. The Master Data Analyst will be the gatekeeper to all master data and is critical to the overall success of the organization. This position is responsible for overseeing key processes and projects associated with the accuracy, integrity and timeliness of critical master data domains. The analyst will take an active role in fulfilling the additional demand generated by the organization changing into to a data-driven company and help develop the tools to educate and empower stakeholders. Analysts in this position are also responsible for analyzing large amounts of data to develop data management recommendations, effectively communicating related results and implications of the various options across multiple integrated teams. etc. | 2/11/2020 |
| 12403 | Bioventus Union County, NJ Associate Sales Representative - New Brunswick, New Jersey BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 12404 | Bioventus Brooklyn, NY Associate Sales Representative - Brooklyn, NY BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 12405 | Bioventus Peoria, IL Associate Sales Representative - Brooklyn, NY BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 12406 | Bioventus Rockford, IL Associate Sales Representative - Rockford, IL BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 12407 | Bioventus Worcester, MA Associate Sales Representative - Worcester, MA BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 12408 | Bioventus Honolulu, HI Sales Rep - Hawaii BS/BA in sports medicine or life sciences Exp: 1-3 year(s) |
The Sales Representative plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. They also educate patients on the proper use of our products. The Sales Representative is fully responsible for managing their own territory – a role that’s perfectly suited to highly motivated self-starters with an entrepreneurial spirit! Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. They are good team players, dynamic, optimistic, accurate, well-organized, and ambitious about developing as a sales professional. etc. | 2/11/2020 |
| 12409 | Bioventus Bozeman, MT Sales Rep - Montana BS/BA in sports medicine or life sciences Exp: 1-3 year(s) |
The Sales Representative plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. They also educate patients on the proper use of our products. The Sales Representative is fully responsible for managing their own territory – a role that’s perfectly suited to highly motivated self-starters with an entrepreneurial spirit! Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. They are good team players, dynamic, optimistic, accurate, well-organized, and ambitious about developing as a sales professional. etc. | 2/11/2020 |
| 12410 | BioVision Milpitas, CA Sales Representative BS/MS in biochemistry, cell biology, or molecular biology Exp: 1-2 year(s) |
BioVision, Inc., a privately held Life Science company, develops and offers world-wide, a variety of products including assay kits, antibodies, recombinant proteins & enzymes, and other innovative research tools for studying Apoptosis, Metabolism, Cell Proliferation, Cellular Stress, Cell Damage and Repair, Diabetes, Obesity and Metabolic Syndrome, Stem Cell Biology, Gene Regulation, Signal Transduction, etc. We are looking for a highly motivated individual to work in our Sales & Marketing Department. etc. | 2/11/2020 |
| 12411 | Blade Therapeutics San Francisco, CA Clinical Trial Associate, Clinical Operations BS/BA in the life sciences or related Exp: 1-2 year(s) |
The Clinical Trial Associate (CTA) will work within the Clinical Operations Team to implement and maintain clinical trials in phases I-IV, as applicable. The CTA will be responsible for adhering to all Blade and/or vendor Standard Operating Procedures (SOPs), in addition to ICH GCP and any applicable, regional/global regulatory authority procedures. This is an in-house role, based out of South San Francisco, CA. The CTA will have the benefit of working with a tight-knit team to drive projects and meet deliverables. In addition to working within the Clinical Operations team, the CTA will also be responsible for some cross-functional interaction. etc. | 2/11/2020 |
| 12412 | BlueRock Therapeutics Toronto, ON Research Associate, Immunology MS in immunology, cell biology, or molecular biology Exp: 1 year |
We are seeking a Research Associate for our Translational Immunology Team. This position will report to the Scientist of Translational Immunology and will have various responsibilities for hands-on lab work, developing T cell, NK cell and myeloid cell assays. This is an outstanding opportunity for a talented associate to contribute to bringing a new class of cellular therapies to patients and gain valuable career experience in Translational Immunology in the life sciences industry. We are seeking a Research Associate for our Translational Immunology Team. This position will report to the Scientist of Translational Immunology and will have various responsibilities for hands-on lab work, developing T cell, NK cell and myeloid cell assays. etc. | 2/11/2020 |
| 12413 | Boston Analytical Cambridge, NH Analytical Chemist *All-Levels* BS in chemistry or related Exp: 0-5 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. Primary Duties and Responsibilities: Prepares and analyzes products to determine chemical and physical properties. Documents work in a clear and organized manner. Follows all safety rules and regulations and conducts periodic safety audits. etc. | 2/11/2020 |
| 12414 | Boston Analytical Cambridge, NH Microbiologist BS/BA in microbiology or related Exp: 0-2 year(s) |
The QC Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. Primary Duties and Responsibilities: Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity). Performs genetic analysis of microbial growth to determine Genus/Species of unknown isolates. Collects Environmental Monitoring Samples onsite and offsite at client manufacturing sites. Documents work in a clear and organized manner. etc. | 2/11/2020 |
| 12415 | Bristol-Myers Squibb Redwood City, CA Associate Research Scientist 1 / 2 - Immuno-Oncology Translational Discovery Biology MS Exp: Not required for MS candidates |
The Associate Research Scientist will join the Translational Discovery Biology team within the Oncology Discovery organization at Bristol-Myers Squibb in Redwood City, CA to deliver potential biomarker and mechanism of action data for targets in the I-O space. Responsibilities: The qualified candidate is a highly motivated, interactive, and creative individual that possesses the ability to work across a highly matrixed environment to support progression of I-O therapeutic targets. This position will specifically support the identification of potential biomarkers, receptor occupancy, target engagement and pharmacodynamic assays for these targets. Additionally, the position will support mechanism of action studies using primary human tumors and mouse models. etc. | 2/11/2020 |
| 12416 | Brooks South Plainfield, NJ Bioinformatics Scientist MS in bioinformatics Exp: 1-3 year(s) |
Responsibilities: Work collaboratively with bench scientists, comprehend project objectives, evaluate and provide informatics solutions. Develop and implement bioinformatics analyses, applications, and workflows. Integrate statistical analysis to project design and data interpretations. Work closely with IT specialists to build robust infrastructure. Support company intellectual property management. Support NGS with data analysis and delivery, pipeline development and automation. Provide customer support for NGS data analysis results. Support Sales and Marketing departments and related business development efforts. | 2/11/2020 |
| 12417 | Brooks South Plainfield, NJ Laboratory Technician I HS diploma/AS/AA Exp: 1+ year(s) |
Our Lab Techs are: Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. etc. | 2/11/2020 |
| 12418 | Brooks South Plainfield, NJ Associate Scientist, Clinical Development BS in a biological science Exp: 1+ year(s) |
The Associate Scientist position in our Clinical Services department is a great entry-level role with room for growth and advancement. If you have the desire to work in a casual yet results-driven environment that embraces innovation- then you’re just what we’re looking for! Responsibilities: Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. etc. | 2/11/2020 |
| 12419 | Brooks South Plainfield, NJ Sales Associate I BS in a life science Exp: 1+ year(s) |
Responsibilities (maximum 8 key tasks and responsibilities of this position): Conduct marketing and sales independently in academic and small biotech accounts including hall walking, planned meetings, vendor shows, lunch and learns, and cart shows. Conduct sales strategy, account management, partnership negotiations, and phone/email prospecting under the direction of the manager/team lead. Achieve defined metrics for sales activity revenue growth in assigned accounts. Update price lists, create new price lists, and write quotes. Execute CDA's, service agreements, and other documents. etc. | 2/11/2020 |
| 12420 | Brooks South Plainfield, NJ Inside Sales Associate BS in a life science Exp: 1+ year(s) |
The Sales Associate is expected to grow the revenue and expand the GENEWIZ brand in the assigned territory/accounts with strong support, direction and mentoring by the Assistant Manager, Inside Sales Team. Key work interactions (main interfaces with who the jobholder will have regular contact): Co-workers, Managers, Customers. Responsibilities (maximum 8 key tasks and responsibilities of this position): Achieve annual sales goals within defined territory/ accounts. Develop and implement an effective territory business growth plan. Conduct sales and marketing activities independently in academic and biotech accounts. Conduct sales strategy, account management, partnership negotiations, and phone/email prospecting under the direction of the manager. etc. | 2/11/2020 |
| 12421 | Brooks South Plainfield, NJ Associate Scientist I BS in a biological science Exp: 1+ year(s) |
The Associate Scientist position in our Next Generation Sequencing department is a great entry-level role with room for growth and advancement. If you have the desire to work in a casual yet results-driven environment that embraces innovation- then you’re just what we’re looking for! Responsibilities: Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. Communicate with customers by phone and e-mail in a friendly and professional manner. etc. | 2/11/2020 |
| 12422 | Brooks Cambridge, MA Laboratory Technician I HS diploma/AS/AA Exp: 1+ year(s) |
Our Lab Techs are: Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. Customer focused. Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. etc.Our Lab Techs are: Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. Customer focused. Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. etc. | 2/11/2020 |
| 12423 | Sarepta Therapeutics Andover, MA Associate I, Oligonucleotide Chemistry BS in chemical engineering/organic chem, etc. Exp: 1 year in organic chem lab |
The Associate I, Oligonucleotide Chemistry will work on a rapidly growing team focused on supporting internal Research and Discovery, Analytical Development, Pre-clinical, and Toxicology groups. This role will perform high throughput synthesis, purification, and isolation of Sarepta’s phosphorodiamidate morpholino oligomers (PMOs). The Research Manufacturing Oligonucleotide Chemistry group synthesizes PMOs for lead-candidate screening, Analytical standards, and commercialization support. | 2/9/2020 |
| 12424 | Sarepta Therapeutics Cambridge, MA IT Support Specialist I HS Diploma/GED Exp: 1-3 years in technical support |
Level I Specialist primary duties include Tier 1 technical support, including software/hardware installation, troubleshooting, hardware break/fix, VoIP phone support and asset management. Provide Tier 1 technical assistance for computer hardware, software systems, and printers/copiers. Analyze, troubleshoot and resolve reported issues (software, hardware, and processes) in a logical and systematic method | 2/9/2020 |
| 12425 | Sarepta Therapeutics Andover, MA Research Associate I, Translational Development BS in biological/chemical sciences Exp: 1-3 years lab experience |
The qualified candidate will provide laboratory support, perform experiments to develop and validate bioanalytical assays and perform analysis of tissue in support of Sarepta’s clinical trials. This person will be expected to work within the framework of a GCLP-compliant laboratory, maintain good documentation practices, and adhere to standard chemical and biohazard safety guidelines while working in the laboratory. | 2/9/2020 |
| 12426 | SCA Pharma Little Rock, AR IV Compounding Technician (1st Shift) HS Diploma/GED Exp: 1 year in pharma environment |
This Team Member will undergo stringent training program to become qualified to work in aseptic environment inside ISO 7 rooms and ISO 5 workspaces ensuring admixtures are completed properly per FDA and cGMP requirements. Undergo thorough training curriculum on gowning, compounding, aseptic manipulations, USP 797 regulations, FDA cGMP-503B regulations, media fills, internal SOP's. | 2/9/2020 |
| 12427 | SCA Pharma Little Rock, AR Aseptic Sanitization Specialist (3) HS Diploma/GED Exp: 1 year in pharma |
The Aseptic Sanitization Specialist will be responsible for sanitizing products prior to them entering the cleanroom. The position will also ensure that the detail, scheduling, and methods of cleaning are sufficient according to the standard operating procedures to protect the raw materials, products, clean room (material transfer, formulation, bag fabrication and fill rooms) and non-clean room (cart loading, sterilization and pack-out areas) environments from the introduction of microbial contamination or infestation. | 2/9/2020 |
| 12428 | Scantibodies Lab Santee, CA Chemist I BS/BA in life sciences Exp: 0-1 years in labs |
A Chemist I isresponsible for manufacturing products to meet or exceed customers' specifications according to manufacturing procedures by adherence to the Scantibodies Quality System and in compliance to the FDA/ISO 9001 and GMP guidelines, with moderate supervision. This employee is required to assist the supervisor and manager with production improvement, process trouble shooting, and new product development. In addition to regular production activities, this employee also is required to participate in production improvement and research related projects. | 2/9/2020 |
| 12429 | Sciecure Monmouth Junction, NJ QC Document Review BS/BA in chemistry Exp: 1-2 years in GMP lab |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. | 2/9/2020 |
| 12430 | SCIEX Framingham, MA Regulatory Affairs Specialist BS in sciences Exp: 1-4 years in regulatory affairs |
Support the regulatory submission activities to obtain and maintain approvals for commercially distributing in vitro diagnostics products worldwide. Participate in activities to ensure compliance with worldwide regulatory requirements. Key Responsibilities:- Supports Design History File development, reviewing documentation for regulatory requirements and current standards. | 2/9/2020 |
| 12431 | SciQuus San Diego, CA Clinical Trial Associate BS/BA Exp: 1 year in clinical research |
Establish, organize, track, and maintain essential regulatory and clinical trial files. Work with the clinical team to achieve study deliverables by assisting in the review and QC of clinical documents (e.g. protocol, informed consent templates, study manuals, forms, etc.). Interact with clinical trial sites from start-up through study close-out | 2/9/2020 |
| 12432 | Seattle Genetics Bothell, WA Anatomical Pathology Lab BS/BA Exp: 1-5 years in histology |
We are seeking an individual to provide standard services in core histology (tissue trimming, processing, embedding, cutting, and histochemical stains). Organizes a large and varied daily workload, accommodating priority requests, focusing on immediate tasks despite interruptions. Assists with rodent necropsies and grossing of samples. Processes tissue specimen for microscopic examination by using appropriate methods for fixing, embedding, sectioning, staining and mounting | 2/9/2020 |
| 12433 | Seattle Genetics Bothell, WA Quality Control Analyst I/II BS/BA in sciences Exp: 0-4 years in pharma/biopharma |
2/9/2020 | |
| 12434 | Seattle Genetics Bothell, WA Research Associate I/II Analytical Sciences BS or MS in biologica/chemical sciences Exp: 0-3 years |
Seattle Genetics is seeking a Research Associate to participate in the development of drug programs. Responsibilities: Conduct experiments, process/analyze data and report results to relevant parties to support manufacturing process development. | 2/9/2020 |
| 12435 | SDIX Newark , DE Biotechnician I / II (Instrumentation) BS/BA in med tech, biological/chemical sciences Exp: 0-7 years |
Maintain laboratory in proper working order through organization and procurement of supplies, routine maintenance of laboratory equipment, organization and maintenance of reagents, and general laboratory hygiene. Verify and ensure that proper processes and procedures are followed in accordance with SOPs. | 2/9/2020 |
| 12436 | SDIX Newark , DE Technician I / II AS/AA in animal sciences Exp: 0-2 years |
This position participates in a team of technicians responsible for animal husbandry and antibody production activities. All job responsibilities to be conducted within standard operating procedures and regulatory compliance. 1. Clean and disinfect cages, rooms and support areas. 2. Feed animals; maintain water systems, ventilation settings, pest control, and related tasks. 3. Conduct animal identification, animal breeding programs and related tasks. | 2/9/2020 |
| 12437 | Sebela Holbrook, MA QC Chemist BS/BA in chemistry Exp: 0-2 years in cGMP |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. Perform testing of raw materials and products. Perform instrument qualification and maintenance. Perform test method validation/verification. Review analytical data for completeness, accuracy, and compliance. | 2/9/2020 |
| 12438 | Sedia Biosciences Portland, OR MANUFACTURING TECHNICIAN AS/AA in lab discipline Exp: 0-1 years in labs |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. | 2/9/2020 |
| 12439 | Sedia Biosciences Portland, OR QC Technician AS/AA in technical field Exp: 1 year in med devices |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. | 2/9/2020 |
| 12440 | Sedia Biosciences Portland, OR SCIENTIST/ASSOCIATE SCIENTIST (R&D-Product Development) MS in biological/chemical sciences Exp: 1-3 years lab experience |
The successful candidate will be responsible for running laboratory tests, recording data, performing some degree of data analysis, drafting protocols, and communicating with managers from R&D and other departments. They will also be asked to participate in production of prototype products, and assist in transition of those procedures (through training and/or record-keeping) to our manufacturing department. | 2/9/2020 |
| 12441 | Seer Redwood City, CA Mass Spectrometry Research Associate BS or MS in sciences Exp: 1-3 years in lab setting |
The Mass Spectrometry group is focused on using the latest MS and associated instrumentation for proteomics molecular profiling. Areas of specific responsibility and attention will include: Carefully perform procedures on experimental samples derived from blood and blood products, urine, saliva, and other biological fluids or tissues. Perform routine calculations, data entry, and lab notebook maintenance, including electronic notebooks and other data annotation, curation, and storage formats. | 2/9/2020 |
| 12442 | Seer Redwood City, CA Assay Development Research Associate BS or MS in biological sciences Exp: 1 year in molecular biology techniques |
Participate in the design, development, and implementation of biochemical experiments to support assay projects and development of the core protein assay platform, with specific emphasis on proteomic assays such as, ELISA, HPLC and mass spectrometry. Assay development with ELISA and immunoassay multiplexing technology. Duties including assay optimization, sample analyzing, assay troubleshooting, automation support, assay characterization and validation, development of protein based assays, immunoassays, protein arrays, product development of IVD and generating SOPs. | 2/9/2020 |
| 12443 | Sekisui San Diego, CA Mechanical Engineer BS in mechanical/biomedical/materials engineering Exp: 1+ years in class II/III med devices |
The R&D Mechanical Engineer is responsible for assisting in the design and development of innovative instruments and consumables for IVD medical devices. The candidate should be familiar with designing mechanisms, device enclosures, machined or injection molded components, and complex assembly methods. An understanding of material selection to optimize mechanical performance, sterilization effectiveness, and biocompatibility is required. The engineer will contribute to the R&D Engineering Department by owning instrument design solutions, test method development & design for manufacturing. | 2/9/2020 |
| 12444 | Renaissance Lakewood, NJ Associate Microbiologist I BS/BA in natural sciences Exp: 0 years |
The Associate Microbiologist performs various types of microbiological testing under supervision. Evaluates, and records data. Assists lab management and microbiologists as directed. Schedule flexibility is required. This is a salaried position and exempt from overtime pay. | 2/8/2020 |
| 12445 | Renaissance Lakewood, NJ Gown Qualified Operator, 3rd shift BS/BA in natural sciences Exp: 0 years |
The Gown Qualified Operator is responsible for the full spectrum of duties in assigned filing room. This may include but is not limited to: set-up of room and equipment for production, operate equipment to meet product specifications and batch record requirements, ensures correct components and product according to production schedule and batch record, equipment and room cleaning and sanitization, etc This is a 3rd shift position. | 2/8/2020 |
| 12446 | Renaissance Lakewood, NJ Gown Qualified Technical Operator, 1st shift BS/BA in natural sciences Exp: 0 years |
The Gown Qualified Operator is responsible for the full spectrum of duties in assigned filing room. This may include but is not limited to: set-up of room and equipment for production, operate equipment to meet product specifications and batch record requirements, ensures correct components and product according to production schedule and batch record, equipment and room cleaning and sanitization, etc This is a 3rd shift position. | 2/8/2020 |
| 12447 | Repligen Marlborough, MA Manufacturing Associate II - TFF AS in technical discipline Exp: 0-5 years |
Mechanical assembly and testing of custom TFF systems per assembly drawings, SOP’s, and batch records. Point to point wiring, installation of cables, installation of software, and packaging of final product. Operates and maintains production equipment as it relates to manufacturing operations. Maintains records to comply with regulatory requirements. Documents all work on batch records according to Good Manufacturing practices. Performs batch record review as required by Production management | 2/8/2020 |
| 12448 | Repligen Rancho Dominguez, CA Assembler I HS Diploma/GED Exp: 0-1 years in production/manufactruing |
This assembly position performs a wide variety of fiber assembly, filtration product assembly or sub-assemblies. Determines and/or follows methods and sequence of operations in performing fiber bundling, filter potting, filter welding, fitting on assembly units and packaging. The employee also works as a team member in whatever capacity and job function is required to deliver a quality product to our customer in a timely fashion. | 2/8/2020 |
| 12449 | Repligen Waltham, MA Manufacturing Associate II- Biomanufacturing 2nd Shift BS in biological sciences or related Exp: 0-2 years in biotech manufacturing |
This position is for the 2nd shift in the Biomanufacture group, however; cross training into other departments may be required. The successful candidate will play a key role in ensuring that the department’s production and quality goals are met. Applicants must have strong technical knowledge and problem-solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. Experience working in a GMP/document-controlled environment would be beneficial. Attention to detail, and the ability to work in a team environment are essential. | 2/8/2020 |
| 12450 | Repligen Waltham, MA Manufacturing Associate II- Biomanufacturing 2nd Shift BS in biological sciences or related Exp: 0-2 years in biotech manufacturing |
This position is for the 2nd shift in the Biomanufacture group, however; cross training into other departments may be required. The successful candidate will play a key role in ensuring that the department’s production and quality goals are met. Applicants must have strong technical knowledge and problem-solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. Experience working in a GMP/document-controlled environment would be beneficial. Attention to detail, and the ability to work in a team environment are essential. | 2/8/2020 |
| 12451 | Repligen Marlborough, MA Manufacturing Technician HS Diploma/GED Exp: 1+ years in membrane related processes |
. The successful candidate will play a key role in ensuring that the department's safety, Quality, and Production goals are met. Experience working in a classified cleanroom, and knowledge of GMP/ISO/document controlled processes and GDP would be beneficial. Attention to detail, and the ability to work in a team environment are essential. Ability to read and understand standard operating procedures is required. | 2/8/2020 |
| 12452 | ReShape Life Sciences San Clement, CA Administrative Assistant HS Diploma/GED Exp: 1+ years in administrative support |
The Administrative Assistant will assist management and all visitors to the company by handling office tasks, providing polite and professional assistance via phone, mail and e-mail, making reservations or travel arrangements and generally being a helpful and positive presence in the workplace. The Administrative Assistant should be professional, polite and attentive while also maintaining accuracy and willing to meet challenges directly. | 2/8/2020 |
| 12453 | Philips Monroeville, PA Usability Validation Engineer BS/BA in engineering Exp: 1+ years in engineering on med devices |
The selected candidate will work under direct supervision of the Engineering Lead to produce clear and concise validation documents for medical devices. Focus will be designing and conducting usability test programs in accordance with IEC 62366-1 and FDA Guidance “Applying Human Factors and Usability Engineering to Medical Devices” in conjunction with ISO14971. | 2/8/2020 |
| 12454 | Philips Gainesville, FL Assembly Technician 1, Second Shift HS Diploma/GED Exp: 1 year in manufacturing |
Set and operate production equipment for the purpose of assembling our MRI coils during our second shift, 3:30pm to 12:00am. Performing various repetitive electronic assembly operations on components or subassemblies (under supervision). Using schematics or blueprints, wiring lists, and verbal and written instructions to assemble, modify, rework, or reassemble units. Properly executing the established process and the process parameters | 2/8/2020 |
| 12455 | Philips Bothell, WA Clinical Test Engineer-Ultrasound Sonographer AS/AA or BS/BA Exp: 1+ years in clinical ultrasound |
As a member of an Agile SCRUM team, execute systems/software tests and test procedures in support of product development testing on ultrasound systems. Test Procedure execution. Test data generation/review/approval. Operating ultrasound products in a black box and white box fashion to identify defects | 2/8/2020 |
| 12456 | Rho Durham, NC Research Associate BS/BA in sciences Exp: Entry Level |
The Research Associate will assist project managers in day-to-day operations of either federally-funded or commercial studies. This is an entry-level position. This is not a laboratory research position. The position will offer the opportunity to participate in all aspects of clinical research support, including document preparation, maintenance, and filing; meeting coordination and support; and data management activities including data entry and review. | 2/8/2020 |
| 12457 | Rockland Limerick, PA Associate Scientist (Quality Control) BS/BA in biological/chemical sciences Exp: Entry Level |
We are seeking a talented and highly motivated team player as an addition to our Quality Control (QC) Department. The applicant should be highly motivated, demonstrate broad scientific knowledge, problem solving and troubleshooting skills, show attention to details, high level of independence and display a fundamental understanding of immunoassays. | 2/8/2020 |
| 12458 | Roviant Sciences New York , NY Associate Data Engineer BS/BA Exp: 1-3 years with coding |
We are seeking a thoughtful, hands-on Data Engineer to join Roivant's Data Architecture team. Data Architecture is a broad team that develops and operates the data platform used by developers throughout the Roivant family. You will join a small team partnering with product owners and developers at Roivant and Vants to provide end-to-end data solutions for technology tools and products.You will automate and maintain data processing pipelines, implement modern ETL infrastructure, and continuously improve the efficiency of our platform. | 2/8/2020 |
| 12459 | RS Medical Shreveport, LA Field Support Representative HS Diploma/GED Exp: 6 months in clinical/hospital/med office setting |
The Field Support Representative works with a Sales Account Manager within a defined sales account base to assist and support in clinical and administrative duties. Support the daily order flow within established sales accounts. Schedule patient education sessions in a timely manner. Control and account for all product inventory. Conduct patient education sessions within a clinical setting on the use of the prescribed RS Medical product. | 2/8/2020 |
| 12460 | Rubius Therapuetics Cambridge, MA TEMP - Associate Engineer BS in biochem/biomedical engineering/pharma sciences Exp: 0-2 years |
We are seeking an Associate Engineer (contract) to support solution preparation and process support activities within the upstream and downstream process development of Red Cell Therapeutics at our Cambridge, MA location. This associate will perform tasks including preparation and characterization of raw material stock solutions, upstream media formulations, and downstream process buffers while also contributing significantly to the buildout of infrastructure, workflows, and procedures needed to ensure consistent delivery of solution requests and traceable documentation of all source materials. | 2/8/2020 |
| 12461 | Virscio New Haven, CT Laboratory Technician BS in biological sciences or related Exp: 1 year in lab |
The position will additionally involvemanaging the receipt, storage and processing of biological specimens and thepackaging and shipment of samples. These activities will involve accurate tracking of samples, adherence to internal standard operating procedures (SOPs), preparing required sample and reagent dilutions, maintaining logbooks and complying with GLP laboratory standards. | 2/8/2020 |
| 12462 | Sagent Pharmaceuticals Schaumburg, IL Contracts Analyst BS/BA Exp: 1 year in contract/finance/data entry |
General support in the processing of daily paperwork and maintenance of the contracts database. Ability to accurately complete tasks in a timely fashion in a busy environment and often with changing priorities. Data Entry into the Contract Database: product, pricing and customer updates | 2/8/2020 |
| 12463 | Salubris Bio Gaithersburg, MD Associate Scientist/Scientist-Downstream Process Development MS in bio/chemical engineering Exp: 1+ years |
Develop robust and scalable downstream processes in laboratory scales for the purification of antibodies or antibody-based therapeutic proteins with chromatography (affinity, IEX and/or HIC, etc.). Support scale-up of downstream processes and technology transfer to cGMP manufacturing facilities for clinical material production, work with cGMP manufacturing team to generate and review SOPs and batch record for traceability. | 2/8/2020 |
| 12464 | Samumed San Diego, CA Clinical Trials Assistant (CTA) BS/BA in life sciences or healthcare Exp: 0-2 years |
Samumed is looking for an intelligent and enthusiastic individual to join its Clinical Development team as a Clinical Trials Assistant. The Clinical Trials Assistant will provide administrative support to the Clinical Operations team across the company's ongoing clinical studies. Manage the set-up of studies and sites in the electronic Trial Master File (eTMF). Manage the set-up of studies and sites in the Samumed Grant Payments Application | 2/8/2020 |
| 12465 | Sanofi Ridgefield, NJ Aseptic Technician Associate HS Diploma/GED Exp: 1-3 years in cGMP environment |
Aseptic Technician Associate will Independently perform the tasks of the production operation specific to aseptic manufacturing, filling, and packaging. Maintains batch record documentation and logs as required by corporation and regulatory agencies. Performs cleaning and sanitizing of production equipment and classified production space. Prepares, according to procedures, various stock solutions and buffers as required by the production process. | 2/8/2020 |
| 12466 | Sanofi Swiftwater, PA Maintenance Technician 2 year trade certificate in HVAC or general mecahnics Exp: 0-1 years |
The Maintenance Technician is responsible for supporting the design, installation, maintenance, troubleshooting and repair of all site-wide equipment in order to maintain a Quality Class A environment in GMP facilities. This position will have interactions with HSE, Engineering, Outside Contractors/Consultants, Industrial Operations and Research & Development departments. | 2/8/2020 |
| 12467 | Sanofi Swiftwater, PA Maintenance Technician 2 year trade certificate in HVAC or general mecahnics Exp: 0-1 years |
The Maintenance Technician is responsible for supporting the design, installation, maintenance, troubleshooting and repair of all site-wide equipment in order to maintain a Quality Class A environment in GMP facilities. This position will have interactions with HSE, Engineering, Outside Contractors/Consultants, Industrial Operations and Research & Development departments. | 2/8/2020 |
| 12468 | SCBT Dallas, TX Warehouse Associate/Coordinator AS/AA or BS/BA Exp: 1-2 years |
This position assists in the daily processing, picking, packaging and shipping of domestic and international orders. SCBT maintains a climate controlled warehouse (heated/cooled) making for a comfortable work environment year round. SCBT’s products are generally small and lightweight commodities that are easily handled and processed for shipment. This is a full time position with career advancement opportunities within the company. | 2/8/2020 |
| 12469 | SCBT Santa Cruz, CA Laboratory Assistant BS/BA in biological sciences Exp: 0-2 years |
This is an opportunity to get a jumpstart in the biotechnology industry and gain practical work experience while attending school at the same time. This position will perform routine tasks in support of analytical and preparative procedures required for the purification, analysis of antibodies and associated reagents used in the scientific community. | 2/8/2020 |
| 12470 | SCBT Sun Valley, ID Research Assistant BS/BA in biological sciences Exp: 0 years |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Ketchum, ID campus. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from lab supervisor. | 2/8/2020 |
| 12471 | SCBT Santa Cruz, CA Research Assistant BS/BA in biological sciences Exp: 0 years |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Ketchum, ID campus. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from lab supervisor. | 2/8/2020 |
| 12472 | SCBT Paso Robles, CA Research Assistant BS/BA in biological sciences Exp: 0 years |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Ketchum, ID campus. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from lab supervisor. | 2/8/2020 |
| 12473 | Biodesix Boulder, CO Billing Specialist I HS diploma/BS/BA Exp: 1+ year(s) |
Billing Specialist I will be responsible for obtaining necessary patient information to submit on medical claims sent to insurance plans. They will make phone calls to insurance plans and facilities, accurately record information obtained in patient files, and submit claims and appeals to insurance on behalf of patients. Billing Specialist I will work closely with Customer Support Patient Advocates and Billing Team to ensure accurate information is recorded and billing concerns are addressed. etc. | 2/4/2020 |
| 12474 | BioFire Diagnostics Salt Lake City, UT Cost Accountant I BS/BA in accounting or related Exp: 1 year |
BioFire Diagnostics, LLC. is looking to add a Cost Accountant to our growing Finance and Accounting team! This Cost Accountant is responsible for assisting with the planning, implementation and maintenance of the cost accounting system. Major responsibilities include accurate and timely analysis, as well as contributing to reporting and compliance activities. Essential Job Duties and Responsibilities: Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics’ Quality System. Monitor inventory activities from purchase of raw material through the production process to finished goods. Assist with tracking and reporting scrap and supply expense. Support cost system development and associated internal controls. Assist with preparing the monthly, quarterly and year-end close, prepares related reports and presentations and meets reporting deadlines. etc. | 2/4/2020 |
| 12475 | BioFire Diagnostics Salt Lake City, UT ETL Developer I BS/MS in computer science or related Exp: 1+ year(s) |
BioFire Diagnostics, LLC. is looking for an ETL Developer I to join our growing team! The ETL Developer will analyze, design, develop, test and maintain the data pipeline component of BioFire’s Data Warehouse. This includes refinement of stored procedures to improve daily and real-time data loads in effort to make them more efficient and scalable. ETL Developer will work closely with BI Analysts and Engineers to build a Data Warehouse that provides quality, accurate, accessible and governed data capable to deliver business insight to various BioFire business domains through reporting, dashboards and visualizations. ETL Developer will promote Kimball methodology and utilize current technology stack to find innovative solutions to complex data problems. Ability to work as a team player alongside a talented group of individuals for the same cause is essential to success in the role. etc. | 2/4/2020 |
| 12476 | BioFire Diagnostics Salt Lake City, UT Manufacturing Engineering Stock Room Attendant I - Night Shift HS diploma or equivalent Exp: None required |
BioFire Diagnostics, LLC. is looking to add a Manufacturing Engineering Stock Room Attendant to join our growing night shift Manufacturing Engineering team! The Manufacturing Engineering Stock Room Attendant I works within a Manufacturing Engineering Team – generally under the leadership of a more experienced individual (e.g. Engineers and/or Managers). The attendant I uses experience and knowledge to perform the types of activities which are generally considered within Spare Parts Inventory. The Manufacturing Engineering Stock Room Attendant I is expected to work and communicate well with other team members and leadership as assigned in order to meet the goals of the department, the project, and the company. etc. | 2/4/2020 |
| 12477 | BioFire Diagnostics Salt Lake City, UT Manufacturing Engineering Technician Trainee HS diploma/AS/AA Exp: None required |
BioFire Diagnostics, LLC. is looking for a Manufacturing Engineering Technician Trainee to join our growing team! This engineering technician works within a manufacturing engineering team under the leadership of a more experienced individual. This engineering technician uses experience and education to perform the types of technician activities which are within the realm of manufacturing engineering technician and This engineering technician is expected to work and communicate well with other team members and leadership as assigned in order to meet the goals of the project, the department, and the company. etc. | 2/4/2020 |
| 12478 | BioFire Diagnostics Salt Lake City, UT Manufacturing Technician I - Swing Shift HS diploma or equivalent Exp: 6+ months |
BioFire Diagnostics, LLC. is currently in need of Manufacturing Technician I's to work our swing shift schedule of 3:00 PM - 11:30 PM Monday - Friday. This position is responsible for manufacturing products efficiently, accurately, safely, and on time. Operates manufacturing equipment and in-process instrumentation to manufacture regulated products in accordance to QSRs, company policy, and safety regulations. Works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. This position requires attention to detail and relies on instructions and pre-established guidelines to perform the functions of the job. Requires direct supervision or oversight by a senior employee. etc. | 2/4/2020 |
| 12479 | BioFire Diagnostics Salt Lake City, UT BioReagents Formulator - Day Shift AS Exp: 1+ year(s) |
This is a full-time non-exempt position. Responsible for manufacturing and formulation of all BioReagents products and sub-assemblies including Film Array. Operates production equipment and performs duties under compliance of cGMP manufacturing. Weighs, measures, and checks raw materials to assure that manufactured batches, lots, buffers and sub-assemblies contain the proper reagents and qualities. Has knowledge of commonly used concepts, practices, and procedures including PCR, RT-PCR real-time PCR, and use of fluorescence based nucleic acid detection techniques. Assists in complex functional testing and troubleshooting product, process material or formulation processes. Applicant must be mathematically competent, detail orientated, and able to follow written directions well. etc. | 2/4/2020 |
| 12480 | BioFire Diagnostics Salt Lake City, UT BioReagents Formulator - Swing Shift AS Exp: 1+ year(s) |
This is a full-time non-exempt position. Responsible for manufacturing and formulation of all BioReagents products and sub-assemblies including Film Array. Operates production equipment and performs duties under compliance of cGMP manufacturing. Weighs, measures, and checks raw materials to assure that manufactured batches, lots, buffers and sub-assemblies contain the proper reagents and qualities. Has knowledge of commonly used concepts, practices, and procedures including PCR, RT-PCR real-time PCR, and use of fluorescence based nucleic acid detection techniques. Assists in complex functional testing and troubleshooting product, process material or formulation processes. Applicant must be mathematically competent, detail orientated, and able to follow written directions well. etc. | 2/4/2020 |
| 12481 | Biogen Cambridge, MA Operations Associate I, In-Vivo Resource Center AS/BS in animal science or related Exp: 0+ years |
Job Description: Perform daily health observations and effectively record and communicate abnormalities to the scientists. Perform husbandry duties for rats and mice. Perform daily census, handle related documentation and follow reporting procedures. Perform animal receipt and housing of animals. Utilize internal databases to perform the receipt of animals and processing of supplies. etc. | 2/4/2020 |
| 12482 | Biogen Research Triangle Park, NC Senior Instrumentation and Calibration Technician I (Metrology) AS in electronics or instrumentation Exp: Not necessary for AS candidates |
Due to continued growth and the introduction of new technologies across the site, we are looking for a qualified candidate to support the Instrumentation and Controls (I&C) Dept. in a GMP and Non-GMP environment. In this role you will be responsible for performing corrective and preventative calibrations on manufacturing and laboratory analytical instrumentation as well as supporting manufacturing and laboratory personnel in the use, maintenance and repair of on-site instrumentation and test equipment. Applicants will become trained and skilled in all unit operations in their area and performs most functions with minimal supervision. etc. | 2/4/2020 |
| 12483 | Biogen Cambridge, MA Engineer I, Pilot Cell Culture, Gene Therapy BS/MS in bioengineering, chemical engineering, biochemistry, or related Exp: 0-2 years |
Engineer I position within the Gene Therapy BioProcess Development Pilot Facility. Candidate must be motivated and innovative with exceptional analytical and communication skills. Essential Responsibilities: 1) Assist with scale up design and execute laboratory experiments with minimal guidance. 2) Perform independent data recording, analysis, and troubleshooting. 3) Establish manufacturable large-scale cell culture operations. 4) Document development work in concise reports and provide project updates in written and oral presentations. etc. | 2/4/2020 |
| 12484 | Biogen Research Triangle Park, NC Engineer I, Validation BS in a relevant discipline Exp: 1-2 year(s) |
The Validation Engineer I designs and develops validation protocols in addition to provides expertise to associated equipment and automation design / modifications. Additional responsibilities include but are not limited to: Coordinates Equipment & Cleaning Validation Protocols (development & management) for specific equipment areas – including presentation of technical training & support to personnel, with on-floor guidance. Leads validation innovation project efforts requiring cross-functional & contract resources. etc. | 2/4/2020 |
| 12485 | Biogen Cambridge, MA Associate Scientist II/Engineer I, Technical Development BS/MS in bio/chemical engineering or a life science Exp: 0-3 years |
This position will focus on development of high productivity and robust cell culture processes through classically and statistically designed experiments. The candidate’s goals will be to increase process robustness and productivity through comprehensive understanding of levers important to mammalian cell culture. A major component of the role will involve conducting and documenting laboratory bioreactor experiments with a focus on process definition and understanding, experimental design and troubleshooting, and data analysis. etc. | 2/4/2020 |
| 12486 | BioLegend San Diego, CA Manufacturing Technician- Recombinant Antibody & Protein AS/BS in a life science or related Exp: 1+ year(s) |
This position is responsible for manufacturing cutting edge recombinant protein research products in Molecular Cellular Immunology (MCI) group. The successful candidate will be involved in routine task of cell culture, plasmid DNA isolation, buffer preparation, equipment maintenance and support inventory management. Another part of the job responsibility includes transferring the products to other groups for testing, preparing product/project related documentation, and maintaining the inventory and record for recombinant protein products. etc. | 2/4/2020 |
| 12487 | BioLegend San Diego, CA Manufacturing Support Technician - Brilliant Violet Conjugation HS diploma/AS in a life science Exp: 1+ year(s) |
BioLegend develops world-class, cutting-edge antibodies and reagents for biomedical research, manufactured in our state-of-the-art facility in San Diego, CA. Our mission is to accelerate research and discovery by providing the highest quality products at an outstanding value, along with superior customer service and technical support. Our product expertise covers a diverse set of research areas including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology. The Manufacturing Support Technician position will be a key member of our Manufacturing team and will work closely with the BV Conjugation group to assist with the smooth operation of the BV Conjugation laboratory. etc. | 2/4/2020 |
| 12488 | BioLegend San Diego, CA Development Associate - Conjugation BS in biology, biochemistry, or chemistry Exp: 1-3 year(s) |
BioLegend’s Process Development Associate will be responsible for performing all essential functions related to antibody-fluorescence and oligo conjugation, including following Standard Operating Procedures (SOPs) and batch records and maintaining and analyzing lot histories. The Process Development Associate will be an integral member of a team that ensures the highest quality of our finalized antibody products. This position offers the opportunity to gain experience with different types of conjugation chemistries and different chromatography methods to purify conjugated antibodies and offers the opportunity to work in small scale to large scale product projects and to learn to utilize the (Enterprise Resource Planning) ERP database to track production schedules and deadlines and to enter production results. etc. | 2/4/2020 |
| 12489 | BioLegend San Diego, CA Bottling Technician - Formulation Group (2nd shift 3:30pm - 12:00am) HS diploma or equivalent Exp: 6+ months |
BioLegend is looking for a Bottling Process Technician for our Formulation Group. This role will be responsible for processing product formulations, filling, capping, labeling, and completing batch records, and putting away Finished Good Inventory (FGI). This is a highly team oriented group which involves working closely with other core teams within the Bottling Department as well as other departments such as Planning, Receiving, Inventory Control, Custom Solution Team (CST), Packaging and Quality Control groups. etc. | 2/4/2020 |
| 12490 | BioLegend San Diego, CA Research Associate (Cell Analysis) BS in a life science or related Exp: 1 year |
We are seeking a self-motivated Research Associate to join our Product Development team in San Diego. The incumbent will actively participate in all the stages of the development, optimization, and validation of new products. The work requires routinely handling small animals and biological samples from animals and human donors. Prior experience in tissue culture, flow cytometry, immunoassays (eg ELISA, Western Blotting), molecular biology techniques (eg PCR, cloning, etc.), data analysis, and project management are preferred. etc. | 2/4/2020 |
| 12491 | BioLegend San Diego, CA Manufacturing Associate - Chemistry BS in chemistry, biochemistry, material science, or related Exp: 1 year |
BioLegend has an opening for a Manufacturing Associate in our Chemistry group for our MojoSort Product Development team. The main responsibility for this position will be to assist in the large-scale manufacturing of magnetic nanoparticles conjugated with proteins such as streptavidin and antibodies according to established Standard Operating Procedures (SOPs). Other duties will include completion of appropriate batch record forms and updating relevant databases. etc. | 2/4/2020 |
| 12492 | BioLegend San Diego, CA Quality Control Associate (2nd Shift) BS in a science Exp: 1 year |
BioLegend has an immediate opening for a 2nd Shift Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. This position will also perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. The selected individual will be required to train during 1st Shift hours prior to switching to a 2nd Shift schedule. etc. | 2/4/2020 |
| 12493 | Biolife Solutions Albuquerque, NM QC Technician - evo Platform BS in a related field Exp: 1-2 year(s) |
Albuquerque based advanced thermal shipping solution manufacturer is looking to hire a full-time Quality Control Technician with starting pay depending on experience. SAVSU Technologies builds integrated, innovative hardware and software solutions designed to protect live cell therapies during transport and storage. Our customers include cell and gene therapy companies, specialty couriers, biotech/biopharma, research institutions, governments, and NGOs. Quality Control Technician at SAVSU Technologies is responsible for maintaining and improving the existing quality management system alongside the Quality Assurance team. etc. | 2/4/2020 |
| 12494 | Biomarin Novato, CA Specialist, QC I (Temporary) BS/BA in the life sciences Exp: 0-3 years |
Coordinate the calibration, maintenance and repair of analytical laboratory instruments and support equipment using the BioMarin’s Enterprise Computerized Maintenance Management System (CMMS). Responsible for the completion of QC equipment related documentations. Perform change request using the BioMarin’s Enterprise Quality Management System (Trackwise). Maintain vendor service contracts using BioMarin’s SpringCM system. Maintain good working relationships with vendors to ensure vendor meets BioMarin’s current and future needs. Work with vendors to troubleshoot equipment. Maintain the laboratory equipment inventory for tracking equipment assets and vendor contacts. etc. | 2/4/2020 |
| 12495 | Biomarin Novato, CA Material Handler I (Temporary) High school diploma/AA/AS/BA/BS Exp: 1-2 year(s) |
Material Handler I will be responsible for sampling, weighing, and dispensing raw materials to produce buffer, solution, and media kits for manufacturing facilities. Material Handler I is also responsible for receiving and verifying materials and ensuring that material storage locations are properly stocked and maintained. Responsibilities include, but are not limited to the following: Receives, verifies and coordinates raw material receipts and returns from warehouses to manufacturing facilities and vice versa. Contact for raw material issues and reconciliation. Coordinates and reconciles raw materials that are in Quarantine. etc. | 2/4/2020 |
| 12496 | Biomarin San Rafael, CA Research Associate I (Temporary) MS Exp: 0-2 years |
Duties: Performing Immunohisotchemical and In Situ Hybridization Assays. Performing basic histologic techniques (including but not limited to): Fixation, Embedding, Sectioning, and Staining. Epifluorescence and Confocal Microscopy. Image Analysis. Assay development and trouble-shooting. Performing mammalian cell line maintenance and cell based assays. Execute and document laboratory procedures and experiments with great attention to detail. | 2/4/2020 |
| 12497 | Biomarin Novato, CA Associate , Manufacturing (Temporary) BS in a related science or engineering Exp: Not necessary for BS candidates |
PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, protein purification and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Demonstrated proficiency Gain experience with automation systems (LIMS, MES, PI, etc.). etc. | 2/4/2020 |
| 12498 | Biomarin Novato, CA Analyst, QC I (Temporary) BS/BA in a biological or biochemical science Exp: 0-2 years |
The Quality Control Microbiology, Environmental Monitoring, Analyst I under direct supervision, is responsible for performing microbiological, biochemical, and chemical evaluations of the manufacturing facilities, utilities, and equipment. With experience they would perform as a back-up for QC In-process and QC Microbial ID testing. Under direct supervision, the incumbent will be primarily responsible for performing environmental monitoring sampling and testing of the facilities, equipment, and utilities under cGMP guidelines. In addition they will be responsible for performing biochemical and microbiological assays of samples under cGMP and GLP guidelines. Work assignments will encompass activities from routine to semi-routine in nature with the ability to recognize deviations from accepted limits and practices. etc. | 2/4/2020 |
| 12499 | Biomerics Athens, TX Engineering Technician HS diploma/BS/BA Exp: 1 year |
Engineering Technician will provide technical support in the design and development of processes needed to manufacture products that are safe and cost effective. RESPONSIBILITIES: Assist Engineering in the design of product and processes that have the capability to be robust and produce parts and assemblies so that the normal distribution is well within specification and yet cost effective. etc. | 2/4/2020 |
| 12500 | Bio-Rad Hercules, CA Field Service Engineer I AS/AA in electronics Exp: 0-1 year(s) |
Bio-Rad is seeking a Field Service Engineer. This position requires up to 75% travel throughout the San Francisco Bay Area. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. Act as customer advocate to ensure satisfaction and repeat business. Maintains company assets including parts inventory and leased vehicle. | 2/4/2020 |
| 12501 | Bio-Rad Seattle, WA Field Service Engineer BS/BA Exp: 1 year |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers in the Greater Seattle Area. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. Act as customer advocate to ensure satisfaction and repeat business. Maintains company assets including parts inventory and leased vehicle. etc. | 2/4/2020 |
| 12502 | Bio-Rad Cincinnati, OH Field Service Engineer BS/BA Exp: 1 year |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers based in Cincinnati, OH traveling 50 – 75%. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. etc. | 2/4/2020 |
| 12503 | Bio-Rad Pleasanton, CA Research Associate II MS in molecular biology, biochemistry, cell biology, or a related life science Exp: 0-2 years |
Bio-Rad’s Digital Biology Center is a multidisciplinary team developing products using our Droplet DigitalTM technology that are having a large impact in both research and healthcare. Every day, scientists and clinicians around the world use our ddPCRTM and ddSEQTM NGS sample prep systems to make new discoveries, and are revolutionizing clinical decision making with break-through liquid biopsy applications. We’re looking for an energetic and talented Research Associate II (IVD Development) to join our team. Responsibilities: You will work in an assay research and development team on new in vitro diagnostic (IVD) oncology tests using state-of-the-art droplet digital PCR (ddPCR) technology, in a multi-disciplinary department that includes assay research and development scientists, hardware engineers and software engineers. etc. | 2/4/2020 |
| 12504 | Bio-Rad Nashville, TN Field Service Engineer BS/BA Exp: 1 year |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers based in Nashville, TN traveling 50 – 75%. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. etc. | 2/4/2020 |
| 12505 | Bioserv San Diego, CA Manufacturing Technician I/II HS diploma or equivalent Exp: 1-2 year(s) |
The Manufacturing Technician is responsible for supporting and performing routine procedures associated with the manufacture of the customer’s product with minimal direction from Supervisor. Manufacturing Technicians responsibilities include performing environmental monitoring, cleaning and sterilizing of glassware, cleaning of clean-room suites, manufacturing preparatory activities and clean-up, assist in formulation, visual inspections, labeling and packaging. They may be aseptically qualified to perform aseptic manufacturing set-up, filtration, filling and closure of product. etc. | 2/4/2020 |
| 12506 | Biotherapeutics Inc. Blacksburg, VA Chemistry Technician BS/BA Exp: 1+ year(s) |
Biotherapeutics Inc. is looking for a highly motivated Chemistry Technician passionate about science and teamwork. The ideal candidate will be well-versed in analytical chemistry skills. Responsibilities: Chemistry Work: Set up a recrystallization pipeline at BioTherapeutics for abscisic acid (ABA) and punicic acid (PUA), with the intention of recrystallizing additional compounds. Conduct recrystallization optimization analytics. Interface with chemistry department with the ABA and PUA development. Setup chemistry work space and keep detailed records of all activities, record these activities in ASANA, the Google Drive, and in a laboratory notebook. etc. | 2/4/2020 |
| 12507 | RegenxBio Rockville, MD Associate Scientist, Formulation and Drug Product Development BS/BA in chemical/biological sciences Exp: 1-3 years |
Execute scientifically rigorous formulation screening, development, stability, and characterization studies to select stable formulations for our proprietary recombinant AAV gene delivery products. Perform laboratory studies to develop and characterize formulations and processes, using a variety of analytical techniques. Generate protocols and reports on the experimental work and deliver progress presentations at the team and department level | 2/3/2020 |
| 12508 | RegenxBio Rockville, MD R&ED Project Coordinator BS in life sciences Exp: 1-2 years in admin/project support |
Develop agendas, draft document meeting minutes, track action items, maintain project decisions and perform all other project management-related activities. Building and maintenance of R&ED Integrated Master Schedules (IMS); identify appropriate task relationships, display critical path and project baseline to track progress. Serve as formatting lead for presentations, abstracts, papers, reports; coordinates the insertion of draft changes from all team members for final text and graphics. | 2/3/2020 |
| 12509 | AMETEK Middleboro, MD Associate Engineer BS/BA in mechanical/electrical engienering Exp: 0-1 years |
Assist in the design and development of SEPs and engineering projects for new and existing products. Identify new designs, methods or processes to reduce cost and improve quality. Associate Engineers will be given a lead role on projects and SEPs with appropriate scope. Provide technical support to vendors, and manufacturing and assembly departments, and assist with the resolution of problems and questions as required. | 2/3/2020 |
| 12510 | AMETEK Wallingford, CT Industrial Maintenance Technician I HS Diploma/GED Exp: 1-3 years |
Maintenance Technician is a multi-disciplined technician responsible for the repair and maintenance of production, support and facility equipment to ensure safe, reliable operation. They also contribute to support activities, continuous improvement efforts and special equipment projects as directed. | 2/3/2020 |
| 12511 | AMETEK Waukegan, IL Production Operator I HS Diploma/GED Exp: 0-1 years |
Performs processing duties as trained in the laser cutting, preparation, cleaning and inspection of production parts while maintaining all necessary production goals and accurate documentation. Maintains a clean work area and good documentation practices at all times. Complies with all relevant safety policies in area and company. | 2/3/2020 |
| 12512 | AMETEK San Diego, CA Technician, Test - PCB HS Diploma/GED Exp: 1-3 years |
To test a variety of assemblies and sub-assemblies of printed circuit boards using various test measurement equipment and automated test systems. Perform basic to intermediate level troubleshooting on digital and analog circuitry to component level. Read schematics and engineering drawing. | 2/3/2020 |
| 12513 | Renaissance Lakewood, NJ Associate Microbiologist I BS/BA in natural sciences Exp: 0 years |
The Associate Microbiologist performs various types of microbiological testing under supervision. Evaluates, and records data. Assists lab management and microbiologists as directed. Schedule flexibility is required. This is a salaried position and exempt from overtime pay. | 2/3/2020 |
| 12514 | Beigene San Mateo, CA Associate, Regulatory Information Management, Regulatory Operations BS/BA in library science, life sciences, computer science, or related Exp: 1-3 year(s) |
The Regulatory Operations Associate supports the regulatory submission process by managing archiving of submission documents both in paper and electronic format, correspondence and communications, data management, and process evaluation and control. All in compliance with applicable regulations, standards, and internal policies and procedures. This position responsible for maintaining the regulatory archive. Essential Functions of the job: Archiving: Manage and maintain submissions and correspondence in the regulatory archive system. Coordinate exchange of records using document sharing platforms. Generate metrics, reports, and dashboards. Reconcile data o Archives/retrieves regulatory documents (both paper and electronic) as necessary. etc. | 2/3/2020 |
| 12515 | Bicycle Therapeutics Lexington, MA Research Associate - Immuno-oncology/Oncology BS/MS in immunology, immuno-oncology, or translation oncology Exp: 1-5 year(s) |
The Research Associate located in Lexington, MA USA will be primarily responsible for developing and executing immune-oncology in vitro and ex vivo assays of Bicycle® T-cell modulators to enhance progress of Bicycle’s oncology pipeline towards the clinic. In this lab-based role, he or she will be a key player in implementing in vitro characterization of lead T-cell modulator series. Key Responsibilities: The successful applicant will have a strong scientific background and hands-on laboratory skills in immunology, immuno-oncology and/or translational oncology with experience in immunological assay development and in vitro pharmacology. etc. | 2/3/2020 |
| 12516 | BillionToOne West Menlo Park, CA Laboratory Technician BS in biology or a clinical science Exp: 6+ months |
BillionToOne (Y Combinator S17) is looking for a Laboratory Technician - Clinical Laboratory Associate (CLA) I to perform UNITY, the only non-invasive prenatal test that can detect inherited disorders such as sickle cell disease, spinal muscular atrophy, and cystic fibrosis in the baby directly from maternal blood. You will join our growing CLIA team responsible for processing of pregnancy blood samples in a high complexity CLIA setting. This is a full-time 12-month contract position with an hourly rate of $25/hr. Hours and days may vary depending upon operational needs. The CLA I is responsible for assisting with the day-to-day operations and equipment maintenance in the Clinical Laboratory. etc. | 2/3/2020 |
| 12517 | Biocare Medical Pacheco, CA Quality Assurance Associate AA/AS/HS diploma Exp: 0-2 years |
Responsible for coordinating various activities related to product design, development, manufacture, and release in compliance with Company’s Quality Management System. Essential Duties and Responsibilities: Ensures the accuracy and completeness of the QA document system, performs daily filing and organizes contents. Coordinates the review and revision of procedures, specifications and forms as well as maintaining and updating the document control and tracking databases. Reviews batch records, QC records, labels and other documentation. Identifies quality improvement opportunities, compliance concerns, identify, prevent and resolve deviations. Coordinates Periodic Procedure Reviews to ensure documents are reviewed as required. Etc. | 2/3/2020 |
| 12518 | Bioclinica Franklin, TN Medical Imaging Services Technician I BS/BA in a science or health related field Exp: 0-1 year |
Primary Responsibilities: Communicates with Clinical Project Managers, Clinical Operations Associates and/or Specialists regarding image quality, deliverables, and data discrepancies. Communicates with Image Analysis Lead, Clinical Operations Manager, and/or Scientific Director regarding troubleshooting of reading systems, image quality concerns, and deliverables. Maintains study-specific reading tracking tools. Attends all central analysis and quality control training sessions. Completes validation of relevant central analysis types by meeting pre-defined validation requirements. Performs quality control of site qualification- scans using phantom or patient, and on-going patient data within study-specific turnaround times to Clinical Project Manager, Clinical Operations Associate, and/or Specialist responsible for the study. etc. | 2/3/2020 |
| 12519 | Bioclinica Princeton, NJ Inside Sales Associate BS/BA Exp: 1-3 year(s) |
The Inside Sales Associate is an in-house sales position supporting the business development efforts across the United States, working closely with the eHealth Business Development team. The Inside Sales Associate will contact clients directly at an early stage of the sales lifecycle to initiate meetings and support the development of the RFP pipeline for the Sales Directors. This position will also be responsible for developing relationships with clients to expand the Bioclinica portfolio with new and existing clients in partnership with the Sales Directors. etc. | 2/3/2020 |
| 12520 | Quidel San Diego, CA Associate Quality Engineer BS in engineering/life sciences/tehnical discipline Exp: 1-2 years in med devices |
The Associate Quality Engineer is responsible for owning and coordinating Quality Engineering functions and activities for the defined processes. This position is also responsible for supporting the Production, Quality Control, Engineering and Quality Assurance departments and the associated activities, which include receiving inspection, in-process inspection, and finished goods inspection in achieving and exceeding company goals and objectives. In addition, this role is responsible for supporting the administration, implementation, and continuous improvement of the quality systems associated with non-conforming materials, inspection control plans, and corrective/preventive action. | 2/2/2020 |
| 12521 | Quintara Biosciences South San Francisco, CA Entry Level Technician BS with lab work Exp: Entry Level |
Located at South San Francisco and Boston, we are expanding and have several entry level technician positions available. We offer competitive wages and growth opportunities within the company. Handle customer samples and perform DNA sequencing and Molecular Biology experiments . Prepare and set up customer sequencing samples. Set up molecular biology experiments as requested or needed | 2/2/2020 |
| 12522 | Quintara Biosciences Boston, MA Sales Representative BS or higher Exp: 0-2 years |
Located at South San Francisco and Boston, we are expanding and have several entry level technician positions available. We offer competitive wages and growth opportunities within the company. Ability to identify qualifying leads. Ability to sell and present company services to customers. Develop and manage relationships with customers. Contribute information to market strategy by monitoring competitive services and reactions from customers; identifying needs to be filled. | 2/2/2020 |
| 12523 | Quotient Sciences Boothwyn, PA Analytical Scientist I BS in chemistry or realted Exp: 0-3 years in pharma lab |
The position may reside in any one of the functional areas and carry out the responsibility under some supervision: Analytical method development, validation, and transfer activities. Formulation development work including Material characterization and physical testing. API/raw material sampling and testing, In-process and finished product testing, cleaning verification swabbing and testing. | 2/2/2020 |
| 12524 | Quotient Sciences Boothwyn, PA Lab Assistant BS/BA preferred, HS Diploma Exp: 0-3 years with chemicals |
The position supports any one of the functional areas and carries out the responsibility under full supervision. Clean and organize laboratory glassware. Dispose solvent waste as per the laboratory procedures. Monitor and maintain lab cleanliness. Make buffers, mobile phases, etc. as directed by the supervisor | 2/2/2020 |
| 12525 | Quotient Sciences Boothwyn, PA Analytical Scientist II MS in chemistry Exp: 0-2 years in pharma lab |
The position may reside in any one of the functional areas and carry out the responsibility under some supervision: Operate and troubleshoot the following instruments/equipment to test pharmaceutical samples. Follow analytical test methods, compendial methods, experimental procedures and SOP’s. Document test results in laboratory notebook, in real-time, and communicate status of test results to supervisor | 2/2/2020 |
| 12526 | QuVa Sugar Land, TX Production Technician - Post Compounding HS Diploma/GED Exp: 1 year in pharma manufacturing preferred |
This position supports daily manufacturing activities for non-sterile and sterile bulk/CSP operations. Perform line clearances, assure equipment is operating correctly, and assure Post Compounding checks are performed according to current SOPs and Batch Record Instructions. Maintains records of every movement of Controlled and Non-Controlled Substances from the point they are received from compounding. Monitors the daily use of Controlled and Non-Controlled Substances throughout the process to assure people and processes are in a continuous state of compliance with DEA regulations, company policies and procedures and safety requirements | 2/2/2020 |
| 12527 | QuVa Sugar Land, TX Quality Assurance Technician HS Diploma/GED Exp: 1-2 years in FDA regulated operations |
The Quality Assurance Technician performs basic QA functions related to verification of incoming and/or outgoing materials. Quality review / verification of critical information related to the receipt of incoming goods or the distribution of finished goods for customer orders. Ensures compliance of incoming materials prior to use in Manufacturing Operations. Supports packaging of finished goods for customer shipments and verifies accuracy of the order | 2/2/2020 |
| 12528 | QuVa Sugar Land, TX Supply Chain Technician HS Diploma/GED Exp: 1-2 years in distribution/warehousing/shipping/etc |
QuVa Pharma is seeking a motivated and organized Supply Chain Technician to complete inventory replenishment process utilizing manual or automated technology. You will be integral in ensuring that inventory is correctly stocked and labeled, protecting the integrity of sterile supplies. Our ideal candidate is highly organized, a master of prioritization and able to shift gears at a moments notice. | 2/2/2020 |
| 12529 | QuVa Sugar Land, TX Compounding Pharmacy Technician HS Diploma/GED Exp: Pharmacy Technician liscensed |
Compounds sterile preparations as per work instructions under pharmacist supervision. Assists in cleaning and maintenance of the work environment. Complies with all state and federal laws, rules, and regulations governing the practice of pharmacy. Ensures cleansing and garbing policy is performed exactly per sterile preparations. | 2/2/2020 |
| 12530 | QuVa Bloomsbury, NJ Quality Systems Specialist HS Diploma/GED Exp: 1-2 years in QA, GMP production |
To maintain and coordinate Quality Systems related documents for compliance with cGMP and company procedures with minimal supervision. To review and write cGMP procedures under supervision. To process changes in controlled batch records via Change Control process. To issue effective documents including procedures, forms and batch records. To process changes to the procedures. | 2/2/2020 |
| 12531 | RefleXion Medical Hayward, CA Software Quality Engineer BS/BA in engineering Exp: 0-7 years in medical product development |
The Quality Engineer for software process supports compliance to IEC 62304, ISO 13485, and ISO 14971 to ensure full adherence to these standards, in addition to the FDA’s Quality System Regulation and software-related guidance. This position represents the Quality Assurance function on product development teams from early design stages through product implementation to manufacturing, ensuring that all products comply with internal, customer, and regulatory requirements. | 2/2/2020 |
| 12532 | Regeneron Tarrytown , NY R&D Associate - Neurodegenerative Diseases MS in neuro/biological sciences Exp: 1+ years |
The successful candidate will be responsible for the design and execution of experiments to understand the mechanisms of neurodegenerative diseases, discover new therapeutic targets and validate novel therapeutic strategies. We are looking to recruit a candidate with in vitro experience and strong in vivo expertise in neuroscience and models of neurodegenerative disease. Perform cell culture and cell-based assays with immortalized cell lines and primary neurons. | 2/2/2020 |
| 12533 | Regeneron Tarrytown , NY Process Development Associate II - Purification Development BS or MS in chemical/biochem engineering or biochemistry Exp: 0-5 years |
The qualified individual will be responsible for purification process development and support purification of various pre-clinical and clinical biological molecules at pilot scale. Development of technology and automation to increase process throughput and efficiency of preclinical manufacturing. Documents experiments, results, and findings in electronic laboratory notebook; presents work at group and department meetings. Maintain instruments and troubleshoot instrumental/experimental problems. | 2/2/2020 |
| 12534 | Regeneron Rensselaer, NY Associate Process Engineer (Filling) BS or MS in engineering Exp: 0 years |
Provides engineering support for the design and development of robust drug product processes that enable the delivery of life transforming medications to patients globally. The individual will support drug product unit operations from primary container development through drug product filling and inspection, with specialization in the development, industrialization, and technical oversight of primary container components. | 2/2/2020 |
| 12535 | Regeneron Rensselaer, NY QA Validation Specialist (Filling Equipment) BS/BA in engineering, chemistry, or life sciences Exp: 0-2 years |
Summary: Validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures. Generates, executes and/or reviews master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria | 2/2/2020 |
| 12536 | Regeneron Rensselaer, NY Associate Biotech Production Specialist BS/BA in life sciences Exp: 0-2 years |
Please note that this would be a 1st shift position, 6:00 a.m.-4:30 p.m., with potential for double weekends. Performs all tasks necessary for the manufacturing operations of both clinical and commercial manufacturing programs. Reviews, edits, completes, and revises completed batch records, Logbooks, and SOPs in accordance with cGMP standards and compliant with written procedure. Includes all aspects of biotech production activities related to cell culture | 2/2/2020 |
| 12537 | Regeneron Rensselaer, NY Process Engineer (Filling) BS or MS in engineering Exp: 0 years |
Provides technical support for the development of robust drug product processes that enable the delivery of life transforming medications to patients globally. The individual will characterize and support drug product unit operations from freeze/thaw through filling and inspection and will be part of a team responsible for development, industrialization, troubleshooting, and validation of drug product processes at our new fill/finish manufacturing site. | 2/2/2020 |
| 12538 | Regeneron Rensselaer, NY QC Stability Technician BS/BA in life sciences Exp: 0-2 years |
Performs a variety of activities to maintain stability chambers and stability inventory in support of the company’s quality program. Ensures that equipment operates in a compliant state; qualified, calibrated and properly maintained. Monitors Environmental Chamber conditions, ensuring continuous documentation. Collaborates with Stability Coordinators and other departments to receive material to be put on stability. | 2/2/2020 |
| 12539 | PSC Biotech Orange County, CA Entry Level CSV Engineer BS/BA in chemical/biomedical engineering Exp: Entry Level |
Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards. Initiate/update GxP and Risk Assessments on system.Author, Initiate, and/or review and approve IT SOPs related to compliance | 2/1/2020 |
| 12540 | PSC Biotech Pomona, CA Entry Level CSV Engineer BS/BA in chemical/biomedical engineering Exp: Entry Level |
Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards. Initiate/update GxP and Risk Assessments on system.Author, Initiate, and/or review and approve IT SOPs related to compliance | 2/1/2020 |
| 12541 | PsychoGenics Paramus, NJ Research Associate 1 - Behavioral Pharmacology BS/BA in life sciences, neurosciences, psychology Exp: 1+ years lab experience |
We are looking for a highly motivated Research Associate in behavioral neuroscience. The successful candidate will work in a team of scientists and researchers supporting the preclinical studies using rodent models and tests. The primary responsibilities of the candidate will include but are not limited to conducting preclinical research of drug abuse liability, pain, cognition, and other assays as needed. The candidate must be capable of working across teams and independently. | 2/1/2020 |
| 12542 | PsychoGenics Paramus, NJ Animal Care Technician HS Diploma/GED Exp: ALAT cert after 1 year employment |
Review, comprehend, and comply with all SOPs, IACUC policies, safety, and quality assurance standards related to assigned work area. Daily husbandry of the rodents in the vivarium to include the provision of feed, water, clean cages, and enrichment. Basic sanitation and maintenance of colony rooms to include sweeping and mopping of animal quarters, rotating animal cages, racks and room supplies for cleaning according to schedule, disinfecting all areas in room. Monitor the health of the animals and report any sick or dead to the PVC and room lab contact staff. | 2/1/2020 |
| 12543 | PTC Therapeutics South Plainfield, NJ Research Associate II, Molecular Biology/Cell Culture MS in biology Exp: 1 year experience |
The Molecular Biologist is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early stage research, the goal of which is applying new state-of-the-art technologies to research projects as well as the advancement of research programs. The Molecular Biologist is also responsible for communicating experimental results to his/her supervisor and the project team. | 2/1/2020 |
| 12544 | PTC Therapeutics Bridgewater, NJ BS/MS Research Associate, Analytical Development - Gene Therapy MS in biological sciences Exp: 0-2 years |
The BS/MS Research Associate, Analytical Development - Gene Therapy is responsible for assay development and/or routine testing including, but not limited to, AUC, qPCR, cell-based assays and immunoassays. S/He is responsible for hands-on lab work, documentation and communicating results to his/her supervisor. | 2/1/2020 |
| 12545 | PTC Therapeutics Bridgewater, NJ BS/MS research Associate, Analytical Development - Gene Therapy MS in biological sciences Exp: 0-2 years |
The BS/MS Research Associate, Analytical Development - Gene Therapy is responsible for assay development and/or routine testing including, but not limited to, AUC, qPCR, cell-based assays and immunoassays. S/He is responsible for hands-on lab work, documentation and communicating results to his/her supervisor. | 2/1/2020 |
| 12546 | PTC Therapeutics South Plainfield, NJ BS/MS Biologist- Gene Therapy MS in biological sciences Exp: 1 year experience |
The successful candidate will be working on cloning, cell expansion, vector production and purification as well as vector characterization. The Gene Therapy Group at PTC is looking for a motivated BS-MS Biologist to join our team. The group provides a stimulating intellectual environment in a supportive atmosphere. The successful candidate will contribute to research efforts focused on applying PTC’s gene therapy platform in the field of rare genetic disorders. | 2/1/2020 |
| 12547 | Pulse Bioscience Hayward, CA Clinical Research Associate BS/BA Exp: 1+ years in supporting clinical research |
The Clinical Research Associates (CRA) is responsible for assigned aspects of clinical monitoring and site management in accordance with the Code of Federal Regulations (CFR) of the Food and Drug Administration (FDA) and the International Conference on Harmonization - Good Clinical Practice (ICH-GCP). Site visits are conducted to assess protocol and regulatory compliance, data reliability, and the proper care and treatment of study subjects. Please note: This is not a remote position. | 2/1/2020 |
| 12548 | Purdue Wilson, NC Pharmaceutical Technician, Rx/Granulation/Blending HS Diploma/GED Exp: 1-5 years |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. | 2/1/2020 |
| 12549 | Purdue Wilson, NC Pharmaceutical Technician, Rx/Granulation/Blending 1st Shift HS Diploma/GED Exp: 1-5 years |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Prepare raw materials, blends, and bulk accountability throughout manufacturing processes. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. | 2/1/2020 |
| 12550 | Purdue Wilson, NC Pharmaceutical Technician, Rx/Granulation/Blending 2nd Shift HS Diploma/GED Exp: 1-5 years |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Prepare raw materials, blends, and bulk accountability throughout manufacturing processes. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. | 2/1/2020 |
| 12551 | Purigen Biosystems Pleasanton, CA Research Associate I/II BS in biological/life sciences Exp: 1-3 years in biotech |
The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. Execute new and standard protocols for performance testing of Purigen’s custom Sample Preparation platform, including instrumentation and microfluidic chip prototypes. Set-up and execute bioanalytical QC assays, including qPCR, RT-qPCR, fragment sizing (e.g. Bioanalyzer assays) and nucleic acid quantitation assays (e.g. Nanodrop, Qubit) | 2/1/2020 |
| 12552 | Pyramid Labs Costa Mesa, CA Manufacturing Technician HS Diploma/GED Exp: 1 year in GMP |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. | 2/1/2020 |
| 12553 | Qiagen Germantown, MD Technical Associate Automated Assembly Ops HS Diploma/GED Exp: 1-3 years in biotech |
The Technical Associate Automated Assembly operations must comprehend and perform assigned automated and manual production tasks according to established Standard Operating Procedures (SOP’s). Responsible for Automated and/or Manual production and assembly procedures in compliance with relevant regulations and SOP’s. Adhere to and accurately complete all production-related documentation. | 2/1/2020 |
| 12554 | Qiagen Germantown, MD Technical Associate - Kit Assembly Operations HS Diploma/GED Exp: 1-3 years |
The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. Responsible for Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. | 2/1/2020 |
| 12555 | Qiagen Beverly, MA Quality Control Technician I BS/BA in biology or biochemistry Exp: 0-2 years |
The Quality Control Technologist I perform assays on products to ensure product quality standards are met. Independently perform assays and evaluate results for product qualification. Adhere to quality control work instructions. Maintain complete, contemporaneous and accurate records of all work performed. | 2/1/2020 |
| 12556 | QPS Newark, DE Associate Scientist I BS/Ba Exp: 0-2 years |
Perform routine lab operations, such as preparing reagents, pipetting, weighing, monitoring, recording, and replenishing supplies. Assist supervisor in performing analysis of drug or other targets in complex biologic matrices. Set-up, use and maintain complex instrumentation. Document experiment details, calculations, results and observations in accordance with GLPs and SOPs | 2/1/2020 |
| 12557 | QPS Newark, DE Associate Scientist I - Bioanalysis BS/Ba Exp: 0-2 years |
Perform routine lab operations, such as sample extraction, preparing reagents, operating automatic liquid handling equipment, pipetting, weighing, monitoring, and recording, in a neat/clean manner. Assist Principal Investigator in performing quantitative analysis of drug and metabolites in biological samples utilizing validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods under GLP regulations. | 2/1/2020 |
| 12558 | Qualicaps Whitsett, NC MR Technician AS/AA in mechanics/electromechanics Exp: 6 months in QA process |
This position is responsible for managing the quality of the capsule product on their assigned machines by monitoring and evaluating the process, observing trends, adjusting/replacing minor equipment and performing general improvements on the capsule manufacturing machines. Maintain all documentation of production batches while on the production floor. | 2/1/2020 |
| 12559 | Quanterix Billerica, MA Kitting Technician (Contract) HS Diploma/GED Exp: 0-1 years |
In the role, process responsibilities include kitting, labeling and inventory activities to support a diverse assay menu. Responsible for meeting kitting schedule requirements within a fast-paced environment with primary activities being: labeling, kitting and inventory accuracy; Support process development and continuous improvement; Maintain integrity of work areas; | 2/1/2020 |
| 12560 | Quanterix Billerica, MA Quality Control Analyst BS/BA in chemistry/biology Exp: 1+ years in med devices/pharma |
Perform sampling, inspection and testing of incoming consumables and raw materials per compendial and non-compendial methods for GMP use in manufacturing. Perform physical inspection of Bulk Reagents and Assay Kits to support Kit release. Monitor, analyze and trend inspection/testing results and quality data | 2/1/2020 |
| 12561 | Quanterix Billerica, MA Manufacturing Associate BS in biological/life sciences Exp: 1+ year in reagent manufacturing |
This role spans a broad range of activities within the manufacturing operations team at Quanterix. In the role, process responsibilities range from complex protein conjugations to diluent formulation and filling and kitting activities to support a diverse assay menu. Responsible for meeting manufacturing schedule requirements within a fast-paced manufacturing operation with primary activities being: bottle/vial filling, buffer diluent formulation and protein conjugation. | 2/1/2020 |
| 12562 | Quidel Beverly, MA Development Associate BS/BA in life sciences Exp: |
Quidel is searching for an Development Associate to join our team in the Beverly, MA location. The Development Associate will participate in Research and Development activities toward development, enhancement, validation, and transfer of molecular diagnostic assays or associated technologies to manufacturing. The responsibilities include activities to support research and new molecular product development and also include activities to support manufacturing reagents for molecular diagnostics products. | 2/1/2020 |
| 12563 | Arthrex Santa Barbara, CA Product Manager - Associate Bachelor's or Master's in business, marketing, or engineering Exp: 0-1 year(s) |
Essential Duties and Responsibilities: Participates in overall marketing, product strategy, research and development requirements, development, and manufacturing coordination for new and emerging products. Works on technical product development, estimates of potential profits, and release to production. Assists in the management of day-to-day progress and maintenance of products. Provides technical expertise and training to other departments in support of product development. Works with Product Team to develop marketing analysis to determine product definitions. Collaborates with a wide variety of functional areas such as sales, engineering, marketing, manufacturing, and operations to develop and provide product definitions responsive to customer needs and market opportunities. etc. | 1/28/2020 |
| 12564 | Arthrex Santa Barbara, CA Technician I HS diploma or equivalent Exp: 1+ year(s) |
Main Objective: Performs production assembly work of light electro-mechanical assembly operations of moderately high complexity with close attention to detail following manufacturing assembly procedures. Essential Duties and Responsibilities: Manufacture electro-mechanical medical products to specified work orders. Follows engineering drawings, manufacturing assembly instructions and standard operating procedures. Inspects own work as well as the work of others. Operate a variety of hand tools and light manufacturing equipment. Perform tasks such as but not limited to installing circuit boards, power supplies, face plates, product labels, cables and wire harness using screws and adhesives. etc. | 1/28/2020 |
| 12565 | Arthrex Sandy Springs, SC Engineer Tech - Manufacturing AS in engineering technology Exp: Not necessary for AS candidates |
Main Objective: Support the development, implementation and improvements of manufacturing processes to produce cost effective quality products. Essential Duties and Responsibilities: Load part number, product structure and router steps in SAP or any equivalent ERP system. Understand correct revision levels of components to upper level and coordinate with planning regarding CR inventory and WIP run-out including effectivity dates. Handle multiple project management at a pre-determined lead-time and prioritize and respond to special assigned projects. Follow thru newly set-up projects to assure smooth production. Use CAD skills to make drawing revisions. etc. | 1/28/2020 |
| 12566 | Arthrex Naples, FL Product Manager Associate - Imaging & Resection Bi-Polar/ RF BS/BA/MBA Exp: 1+ year(s) |
Arthrex is actively searching for a Product Manager Associate, to actively participate in our fast paced and dynamic bipolar RF product line. The candidate will lead our product management initiatives with regards to cross functional product development, product launches, training and sales support. The successful candidate will build relationships with cross functional team members, sales management, sales representatives and surgeons and add value beyond transactional tasks by pursuing creative and innovative opportunities to provide timely, meaningful, market research, product collateral and training materials. Excellent interpersonal and leadership skills along with one year or more of related experience and a Bachelor's degree or Master’s degree are essential for this position. etc. | 1/28/2020 |
| 12567 | Arthrex Chicago, IL Vet Sales Associate BS/BA Exp: 1+ year(s) |
The Arthrex Veterinary Sales Associate is responsible for generating sales of products and equipment to both existing veterinarians and new customers within an assigned sales territory. The Arthrex Veterinary Sales Associate plans and makes sales calls, and selects products and programs that motivate customers to buy products. ESSENTIAL DUTIES AND RESPONSIBILITIES: Call on target, current and prospective customers in order to generate sales, improve market share, and increase income for AVS. Utilize the computer as a sales aid and be competent in the use of Outlook, and the Arthrex Veterinary website. Seek to understand the needs of the veterinarian and clinic and, in turn, select products and services to satisfy those needs. Establish appropriate relationships with veterinarians and clinics. etc. | 1/28/2020 |
| 12568 | Arthrex Naples, FL International Exhibit Coordinator BS/BA Exp: 1-2 year(s) |
To provide administrative and on-site support to the exhibits department, focusing on international logistics and execution. Assist with all pre-planning, onsite and post events tasks. Serve as a liaison to internal and external clients, including employees, vendors and associations. Essential Duties and Responsibilities: Correspond with exhibitor appointed contractors and association meeting organizers on international exhibit requests as needed. Work with marketing project manager on project requests related to international exhibits activities, and assist & update marketing on changes and deadlines. Work with the AXIS project team and Exhibit Data Specialist on details required for of the leads app and list management. Post show download leads generated, run through the Denied Parties List for GTO and distribute to global team members. Coordinate with global partners to collect user data, conference details and focus products to update the AXIS lead system. etc. | 1/28/2020 |
| 12569 | Arthrex Cleveland, OH Vet Sales Associate BS/BA Exp: 1+ year(s) |
The Arthrex Veterinary Sales Associate is responsible for generating sales of products and equipment to both existing veterinarians and new customers within an assigned sales territory. The Arthrex Veterinary Sales Associate plans and makes sales calls, and selects products and programs that motivate customers to buy products. ESSENTIAL DUTIES AND RESPONSIBILITIES: Call on target, current and prospective customers in order to generate sales, improve market share, and increase income for AVS. Utilize the computer as a sales aid and be competent in the use of Outlook, and the Arthrex Veterinary website. Seek to understand the needs of the veterinarian and clinic and, in turn, select products and services to satisfy those needs. Establish appropriate relationships with veterinarians and clinics. etc. | 1/28/2020 |
| 12570 | Astellas Marlborough, MA Research Associate I BS/BA Exp: 0-3 years |
We are seeking a highly motivated Research Associate, who will work on multiple stem cell and exosome related projects at AIRM. The research associate will be supporting cell culture and differentiation needs for the ocular team. They will also provide technical support for cell characterization through qPCR, ICC etc. They will also be supporting the extracellular vesicle (EV) team for multiple projects for EV isolation, characterization, in vivo studies etc. | 1/28/2020 |
| 12571 | AstraZeneca Gaithersburg, MD R&D Associate I/II - Upstream & Downstream - BPD BS/MS in a scientific or engineering discipline Exp: 0-2 years |
As a Research Associate, you would enter a 2-year program that would give you experience creating our new next generation manufacturing process in three areas: upstream process development, downstream process development, and either pilot-scale equipment design, debugging, and automation, or analytical sciences. You would join a team developing AstraZeneca’s Next Generation Manufacturing Platform. You and the team would develop the continuous and integrated purification platform for biological therapeutics, including antibodies, bispecific antibodies, and Fc-fusions. You would apply the Next Generation Manufacturing methods to drug candidates in Phase I, II, and those entering Phase III. etc. | 1/28/2020 |
| 12572 | AstraZeneca Gaithersburg, MD Research Associate II - Lab Support MS in a biological or chemical science Exp: 0-2 years |
As a Research Associate II, you will function as the point person for the procurement and management of laboratory reagents and supplies. Coordinate maintenance of non-computer-based equipment and prepare associated documentation in accordance with GXP; supporting operations of a regulated laboratory that performs PK and ADA bioanalyses in compliance with GLP / GCP guidelines. Specific Responsibilities include: Responsible for the ordering and stocking of laboratory reagents and supplies to meet development, validation and sample testing needs of regulated bioanalytical lab (HBS and GXP compliance). Coordinates across departments, vendors and systems to schedule preventative maintenance, calibration and validation activities of laboratory non-computer-based equipment to ensure GLP compliance. etc. | 1/28/2020 |
| 12573 | AstraZeneca West Chester, OH Aseptic Control Technician - Operations HS diploma or equivalent Exp: 1-2 year(s) |
The Aseptic Control Technician Autonomously performs tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. The position requires operating equipment in various classified/non-classified areas up to a Class 100 aseptic environment and in a laboratory setting. Essential Job Functions: Prepare documentation of activities, actions, and results. Ensure proper documentation practices during job activities. Read SOPs (Standard Operating Procedures) and excerpts from technical documentation. Maintain accurate and complete records (for example: laboratory notebooks, quality records, sample receipts). Complete required training. etc. | 1/28/2020 |
| 12574 | Athenex Clarence, NY Manufacturing Process Operator I (2nd Shift - 2pm to 10:30pm) HS diploma or equivalent Exp: 1-3 year(s) |
Our Manufacturing Process Operator I is responsible for ensuring the accurate production and documentation of pharmaceutical products and maintain a safe manufacturing environment. Essential Job Functions/Responsibilities: Participate in the manufacturing process by performing visual inspection of compounded drug product per procedure. Participate in the manufacturing process by performing labeling and final packaging of drug product. etc. | 1/28/2020 |
| 12575 | Athenex Clarence, NY Manufacturing Process Operator I (1st Shift 7am to 3:30pm) HS diploma or equivalent Exp: 1-3 year(s) |
Our Manufacturing Process Operator I is responsible for ensuring the accurate production and documentation of pharmaceutical products and maintain a safe manufacturing environment. Essential Job Functions/Responsibilities: Participate in the manufacturing process by performing visual inspection of compounded drug product per procedure. Participate in the manufacturing process by performing labeling and final packaging of drug product. etc. | 1/28/2020 |
| 12576 | Athenex Clarence, NY Quality Control Laboratory Technician BS in chemistry Exp: Not necessary for BS candidates |
Support the laboratory workflow in an efficient and effective manner. Support Analytical group in maintaining the laboratory to make work flow more efficient. Essential Job Functions/Responsibilities: Responsible for promoting and maintaining safe and healthy working conditions in his / her assigned work area; instructs and enforces compliance with established safe work practices and procedures; ensures assigned trainees receive appropriate training and information necessary to conduct their activities in a safe and healthy manner. Properly disposes of solvent waste in appropriate containers and disposes of empty bottles in the recycling bins according to health, safety and environmental practices. Performs laboratory, office and maintenance on a routine basis. etc. | 1/28/2020 |
| 12577 | Atreca South San Francisco, CA Research Associate, Antibody Inventory BS/MS Exp: 0-3 years |
In this position, the successful candidate will help manage and maintain Atreca’s antibody inventory by using automated liquid handling technology, database-driven inventory management systems, and equipment used for quality control. The position reports in the Protein Engineering group, and the work will involve interacting with multiple research groups. Furthermore, he/she will perform quality control on received antibodies as well as process them to be used in downstream assays. This very central position will be in a very dynamic and motivated team dedicated to the discovery of novel, antibody-based cancer therapies. etc. | 1/28/2020 |
| 12578 | Atreca South San Francisco, CA Senior Research Associate, Protein Biochemistry (Temporary) BS/MS in molecular biology, biochemistry, cell biology, or related Exp: 1-10 year(s) |
Atreca's IRC technology identifies anti-tumor human antibodies in a highly accurate and precise fashion. Our goal is to apply this technology to elucidate and characterize novel tumor targets and associated biologic processes that were selected for attack by the patient's immune system. In this position, the successful candidate will apply their skills and expertise in protein biochemistry to further understand the unique biology associated with our targets and contribute to the clinical application of our antibodies using protein biochemistry and molecular biology techniques. The candidate will have extensive experience in molecular biology and protein biochemistry as related to the identification and characterization of proteins driving tumorigenesis. etc. | 1/28/2020 |
| 12579 | Atreca South San Francisco, CA Senior Research Associate, Protein Engineering MS in cell biology, immunology, bioengineering or related Exp: Not necessary for MS candidates |
We are seeking a motivated and enthusiastic Research Associate or Sr Research Associate to join our Protein Engineering group. The successful candidate will play a key role in further developing our yeast display platform and applying it to optimize and generate differentiated antibody and bispecific therapeutics. Primary Duties & Responsibilities: Establish yeast cultures and perform flow cytometry assays. Sort libraries of antibody variants by FACS and help with NGS sample preparations. Develop methods for selecting yeast-displayed antibodies bound to cancer cells. Follow laboratory safety guidelines and practices. | 1/28/2020 |
| 12580 | Avion Pharmaceuticals Boston, MA Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 12581 | Avion Pharmaceuticals Brooklyn, NY Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 12582 | Avion Pharmaceuticals Charleston, SC Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 12583 | Avion Pharmaceuticals Charlotte, NC Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 12584 | Avion Pharmaceuticals Chicago, IL Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 12585 | Avion Pharmaceuticals Fayetteville, NC Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 12586 | Avion Pharmaceuticals Flint, MI Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 12587 | Avrobio Cambridge, MA Research Associate (Process Development Group) BS/MS in biology, biochemistry or related discipline Exp: 1+ year(s) |
We are seeking a Research Associate to join an exciting and fast-growing company to develop gene therapies for rare diseases. The successful candidate will join the process development group at Avrobio, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene therapy programs. The individual will develop quantitative assays measuring gene modification in target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will, perform, and analyze experiments for multiple preclinical and clinical programs and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. etc. | 1/28/2020 |
| 12588 | Axsome New York, NY Clinical Trials Assistant BS in a biological or physical science Exp: 1 year |
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. etc. | 1/28/2020 |
| 12589 | Bachem Torrance, CA Quality Assurance Specialist I BS in a related field Exp: 1-2 year(s) |
The Quality Assurance Specialist I fulfills a critical role for Quality Assurance. This individual will conduct real time batch record review, perform internal audits, contribute to GMP system improvements, write technical documents, and review GMP documentation and reports. This individual must also provide GMP and related training. Your Tasks: Review validation protocols, data and reports, as assigned. Coordinate assigned quality systems, such as GMP training program, deviations, CAPAs, or change controls. etc. | 1/28/2020 |
| 12590 | Bachem Torrance, CA Building Services Technician HS diploma or equivalent Exp: 1-3 year(s) |
The Building Services Technician supports the Facilities, Maintenance, and other teams as needed to ensure manufacturing is performed according to schedule and quality demands. Job responsibilities include, but are not limited to, basic maintenance tasks for facilities and equipment, etc. Your Tasks: Follow Standard Operating Procedures (SOPs) and approved directions to perform basic maintenance tasks on facilities and equipment. Follow SOPs and approved directions to clean glassware and equipment used in GMP processes. Maintain cleaning logs and maintenance logs. Maintain stock of parts, supplies, materials, and tools within areas of responsibility. etc. | 1/28/2020 |
| 12591 | Bachem Vista, CA QA Specialist I QA BSD BS in a related field Exp: 1-2 year(s) |
The Quality Assurance Specialist I fulfills a critical role for Quality Assurance. This individual will conduct real time batch record review, perform internal audits, contribute to GMP system improvements, write technical documents, and review GMP documentation and reports. This individual must also provide GMP and related training. Your Tasks: Review validation protocols, data and reports, as assigned. Coordinate assigned quality systems, such as GMP training program, deviations, CAPAs, or change controls. Perform annual product quality reviews and system reviews as assigned. etc. | 1/28/2020 |
| 12592 | BardyDx Houston, TX Holter Analysis Technician HS diploma/AS Exp: 1-3 year(s) |
Currently, we are looking for Holter Analysis Technicians to join our Clinical Services Team who are passionate about cardiac rhythms and helping cardiac patients through our innovative remote patient monitoring body sensor technologies. The right individuals will join a dynamic and fast-paced start-up environment. Ideal candidates will have CCT or CRAT certification or specialize in cardiac rhythm recognition and interpretation skills. Experience with cardiology or electrophysiology can be advantageous. This position requires PC proficiency, excellent written and verbal communication skills, and meticulous attention to detail. This exciting role also provides excellent growth and advancement opportunities along with a bonus incentive program. etc. | 1/28/2020 |
| 12593 | unspecified, NJ Holter Analysis Technician HS diploma/AS Exp: 1-3 year(s) |
Currently, we are looking for Holter Analysis Technicians to join our Clinical Services Team who are passionate about cardiac rhythms and helping cardiac patients through our innovative remote patient monitoring body sensor technologies. The right individuals will join a dynamic and fast-paced start-up environment. Ideal candidates will have CCT or CRAT certification or specialize in cardiac rhythm recognition and interpretation skills. Experience with cardiology or electrophysiology can be advantageous. This position requires PC proficiency, excellent written and verbal communication skills, and meticulous attention to detail. This exciting role also provides excellent growth and advancement opportunities along with a bonus incentive program. etc. | 1/28/2020 |
| 12594 | Bausch Health Clearwater , FL Manufacturing Associate II HS diploma or equivalent Exp: 1+ year(s) |
Perform various operations in the fabrication of intraocular lenses according to production specifications and standards. Responsibilities: Performs various lens fabrication and inspections duties to include operating lathe and milling machines, lens polishing, finished production inspections and primary packaging. Ensure product meets all acceptable criteria per SOP's. Follow all regulatory guidelines and regulations regarding traceability, and safety procedures. Support, encourage and participate in team related activities; report ideas or suggestions to supervisor. Assist in training manufacturing associates using prescribed training methods and tools as assigned by supervisor/management. Report unusual conditions and problems to supervisor and manufacturing lead; practice good housekeeping. etc. | 1/28/2020 |
| 12595 | Baxter Cleveland, MS Quality Lab Assoc I BS in chemistry, chemical engineering, or biology Exp: 0-3 years |
Perform chemical and physical analysis on medical products through all stages of the manufacturing process from incoming raw materials through to product release. Areas include raw materials, initial, in-process and finished products, Stability Program, protocol support, instrumental analysis and instrument calibration/qualifications. Responsibilities also include adherence to regulatory and procedural requirements that govern the operations and products (e.g., Specifications and Cleveland standard operating procedures). etc. | 1/28/2020 |
| 12596 | Baxter Mountain Home, AR Production Technician I (3rd Shift) HS diploma/AS/AA Exp: 0-1+ year(s) |
Cleans, sanitizes and monitors equipment related to assembly, machinery, processing and/or packaging for all local manufacturing operations. Sets up and operates automatic or semiautomatic machines and related equipment in a continuous production/processing operation. Monitors meters, gauges, valves, flow ratios, temperatures, pressures, and/or related controls and guidelines to ensure adherence to production/process specifications. Responsible for executing all processes in production while strictly adhering to cGMP, SOPs, environmental health and safety guidelines and any other related regulations which could apply. Reports any malfunctions or abnormalities and performs all work in accordance with established safety procedures. etc. | 1/28/2020 |
| 12597 | Bayer Indianola, IA Assembler I - 2nd Shift 2:00pm - 10:20pm HS diploma or equivalent Exp: 0-1 year(s) |
The primary responsibilities of this role, Assembler I 2nd Shift 2:00pm - 10:20pm, are to: Assemble various products; Package various products; Performing rework and inspection on the product; Backing up higher-level positions; Awareness of quality standards and ability to identify defects in Products; Recording data related to product quality and traceability; etc. | 1/28/2020 |
| 12598 | Bayer Kansas City, KS Bayer Crop Science OIT Chemical Operator Rotating Shift HS diploma or equivalent Exp: 1 year |
The primary responsibilities of this role, Bayer Crop Science OIT Chemical Operator are: Prepares packaging materials; Read and understand SOP's; Stages raw and finished materials; Takes required samples during production process; contaminates equipment and piping for maintenance or disposal; Utilizes Personal Protective Equipment Matrix; Maintains inventories of disposable, production, and safety related materials; Recognizes material compatibilities; etc. | 1/28/2020 |
| 12599 | Bayer New Orleans, LA Lab Tech AS/BS in chemistry or related Exp: 1-3 year(s) |
The primary responsibilities of this role, Laboratory Technician, are to: Determine conformance to accepted specifications for a particular chemical or physical property; Monitor and verify quality in accordance with statistical process or other control procedures; Perform troubleshooting and calibration of instruments; Prepare reagents, solutions, and standards; Maintain instruments and apparatus according to established procedures to support testing activities of the unit; etc. | 1/28/2020 |
| 12600 | Bayer Myerstown, PA Associate Technician-3rd Shift HS diploma or equivalent Exp: 6+ months |
The primary responsibilities of this role, Associate Technician, are to: Comply with all workplace standards and safety procedures, including lockout tagout, current good manufacturing practices (CGMPS), occupational safety and health administration requirements (OSHA), standard operating procedures (SOPS), and company guidelines; Take ownership of training and learning to develop high performance competencies such as technical skills, communication skills, and skills to build a team-oriented culture; Demonstrate willingness to learn, maintaining qualifications/skills, training team members, motivating and supporting team members, sharing knowledge to continuously improve the process, etc.; etc. | 1/28/2020 |
| 12601 | Bayer St. Louis, MO Agronomic Research Specialist MS in agronomy, engineering, life sciences, or computer sciences Exp: 0+ years |
The primary responsibilities of this role, Agronomic Research Specialist, are to: Collaborate with project team members to deliver detailed experimental protocols that enable advancement decisions by our scientists and placement decisions to our customers; Handle the operation of research equipment, note taking, data management with internal IT systems, comply with regulated seed stewardship standards, complete and/or participate in safety inspections/training and comply with all policies and standard operating procedures; etc. | 1/28/2020 |
| 12602 | Bayer Lubbock, TX Agronomic Research Specialist MS in agronomy, engineering, life sciences, or computer sciences Exp: 1 year |
The primary responsibilities of this role, Agronomic Research Specialist, are to: Responsible for Delivering the highest quality field data as part of North America’s Plant Breeding R&D pipeline by providing optimal trial management, at times working on an internal R&D effort that spans across crops, sites, and a region; Independently Responsible for the implementation of unique and innovative technology solutions designed to improve research design and operations success through the use of new tools and methodologies to improve overall plant breeding phenotyping such as the pilot and use of geospatial systems, agronomic planting and harvesting tools, harvesting shelling systems, and data capture applications; etc. | 1/28/2020 |
| 12603 | PMI BioPharma Solutions Nashville, TN Engineering Maintenance Technician I HS Diploma/GED Exp: 1-2 years maintenance |
Reporting to the Supervisor of Engineering, the Facilities Technician will be responsible for PMI’s maintenance and equipment support activities. The Facilities Technician performs with minimal supervision preventive maintenance, demand maintenance and calibration tasks on critical equipment, utilities, and facilities. | 1/26/2020 |
| 12604 | PMI BioPharma Solutions Nashville, TN Chemist I, Analytical Development BS/BA in chemistry, biology or related Exp: 1-2 years in pharmacueticals |
The Chemist I position, reporting to the Director, Analytical Development, will operate under moderate supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development. | 1/26/2020 |
| 12605 | PolarityTE Salt Lake City, UT Research Specialist I, II, or III BS in biological sciences/technology, or engineering Exp: 0-2 years as research associate or similar |
Under the general supervision of the Director of BME, the Research Specialist I, II or III will support R&D in conducting research projects by contributing to the following: develop protocols for and maintain laboratory equipment; troubleshoot and resolve problems; ensure compliance with lab protocols and safety standards, policies and procedures; performing complex data gathering and analysis. This role serves to assist with conducting pre-clinical research aimed at validating, testing products and discovering, developing innovative medical technologies | 1/26/2020 |
| 12606 | Poly Peptide Group San Diego, CA Quality Control Chemist BS/BA in chemistry or biochemistry Exp: 0-2 years |
Prepare samples for analysis, analyze, and report results. Prepare controlled documentation in support of the sampling, analysis, and reporting of results. Analyze data with respect to standards or to previously determined parameters. Perform sampling and testing of raw materials according to PPL-SD procedures. | 1/26/2020 |
| 12607 | Poly Peptide Group San Diego, CA GC Specialists- Quality Control BS/BA in chemistry or biochemistry Exp: 0-2 years |
Prepare samples for analysis, analyze, and report results. Prepare controlled documentation in support of the sampling, analysis, and reporting of results. Analyze data with respect to standards or to previously determined parameters. Perform sampling and testing of raw materials according to PPL-SD procedures. | 1/26/2020 |
| 12608 | Poseida Therapeutics San Diego, CA Research Technician or Associate Nanoparticle Formulation BS or MS in pharma sciences, bioengineering, chemistry Exp: 1+ years in industry |
his position offers an exciting opportunity to develop non-viral delivery tools for gene editing and gene therapy applications. This person will be engaged in execution of formulation discovery experiments directed toward discovering and developing novel nanoparticle systems for delivering nucleic acids and proteins. Work at the direction of senior Formulation scientists to formulate multi-component nanoparticles encapsulating nucleic acids | 1/26/2020 |
| 12609 | Poseida Therapeutics San Diego, CA Research Associate, In Vivo Gene Therapy MS in immunology or biological sciences Exp: 0+ years |
The Research Associate will play a key role in advancing exploratory gene therapy programs that leverage our cutting-edge piggyBac® DNA Modification technology. Actively participate in our proprietary gene therapy platform technologies to create new human therapeutic candidates. Develop and perform research involving various in vitro and animal laboratory techniques including PCR, ELISA, cell/tissue isolations, microscopy, in vivo procedures and animal imaging | 1/26/2020 |
| 12610 | Poseida Therapeutics San Diego, CA Research Associate, In Vivo MS in biological sciences or pharmacology Exp: 1+ years in biopharmacueticals |
This position offers an excellent opportunity to develop CAR-T in an exciting and dynamic environment focused on cutting-edge technology. This person will be engaged in in vivo activities directed toward discovery and characterization of novel CAR-T for oncology. Execute studies in mice in support of in vivo pharmacology projects, including tumor cell inoculation, tumor measurement by caliper or imaging, i.v. injections, and blood draws | 1/26/2020 |
| 12611 | Poseida Therapeutics San Diego, CA Research Technician, Gene Editing and Gene Delivery BS in biological sciences/technology, or engineering Exp: 0-2 years |
The Research Technician will play a key role in advancing exploratory gene therapy programs that leverage our cutting-edge piggyBac® DNA Modification technology. Actively participate in our proprietary gene therapy platform technologies to create new human therapeutic candidates. Develop and perform research involving various molecular and cell biology techniques including nucleic acid development, transfection, cell culture and transgene expression. | 1/26/2020 |
| 12612 | PPD Richmond, VA Scientist - Cell Culture - Vaccine Sciences MS in biological sciences or pharmacology Exp: 0-2 years |
As a Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and /or biological matrices for stability and analytical testing. | 1/26/2020 |
| 12613 | PPD Middleton, WI Associate Business Systems Analyst II BS/BA Exp: 1-2 years in software environment |
Assists in formulating and defining systems scope and objectives through research and fact-finding combined with a basic understanding of business systems and industry requirements. Analyzes business and user needs and documents requirements. Gathers and writes requirements and design specification for basic to moderately complex systems. Verifies requirements and design comply with industry regulations and SOPs/WPDs. | 1/26/2020 |
| 12614 | PPD Middleton, WI QA Auditor I - Labs BS/BA or AS/AA Exp: 1-2 years in QA or lab experience |
As a QA Auditor I, you will assure the quality of lab data and reports. Conduct internal and/or external audits to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and/or client contractual obligations. Identify and address non-conformance issues. Assist in the delivery of quality services for contracted quality assurance audits, internal site audits, laboratory audits and file audits for clients and projects. Apply company policies and procedures to resolve routine issues. | 1/26/2020 |
| 12615 | PPD Middleton, WI Assistant Scientist BS/BA Exp: 0-2 years previous experience |
As an Assistant Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. | 1/26/2020 |
| 12616 | PPD Richmond, VA Assoc QC Reviewer BS/BA or equivalent vocational qualification Exp: 0-2 years |
The Associate QC Reviewer ensures the quality of laboratory data and reports and reviews chromatographic data and related notebooks as specified by Standard Operating Procedures (SOPs). This position also evaluates data to ensure compliance with analytical methods, client criteria, Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). | 1/26/2020 |
| 12617 | PPD Middleton, WI QA Auditor I - Labs BS/BA or AS/AA Exp: 1-2 years |
As a QA Auditor I, you will assure the quality of lab data and reports. Conduct internal and/or external audits to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and/or client contractual obligations. Identify and address non-conformance issues. Assist in the delivery of quality services for contracted quality assurance audits, internal site audits, laboratory audits and file audits for clients and projects. Apply company policies and procedures to resolve routine issues. | 1/26/2020 |
| 12618 | PPD Middleton, WI Cell Biologist - 1yr Experience BS/BA or equivalent vocational qualification Exp: 1+ years |
As an Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Problem solving with assistance pertaining to extraction and/or instrumentation problems. Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers | 1/26/2020 |
| 12619 | PRA Health Sciences Salt Lake City, UT Medical Research Associate HS Diploma/GED Exp: 1+ year in medical/clinical field |
Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability | 1/26/2020 |
| 12620 | Precision Redwood City, CA Research Assistant - Fresh Biological Samples BS chemical or life sciences Exp: 1-2 years lab experience |
In this role you will: You will process fresh patient specimens and nonclinical samples. You will perform PMBC or cell subset isolations, plasma fractionations, serum separations, cell thawing, cell counting and generating whole blood aliquots. You will receive and process nonclinical samples such as whole blood units and/or leukopaks. | 1/26/2020 |
| 12621 | Prevail New York, NY Clinical Trial Assistant BS in sciences Exp: 1 year in clinical research |
The Clinical Trial Assistant will assist in the delivery of clinical development objectives by providing administrative support to the clinical team and will report to the Director of Clinical Operations. We are looking for an organized, detail-oriented, enthusiastic, self-motivated, hands-on collaborative person with excellent interpersonal skills. | 1/26/2020 |
| 12622 | Principia Biopharma South San Francisco, CA Clinical Trial Associate BS/BA in biological/chemical sciences Exp: 1 year in clinical trial setting |
Responsible for assisting with site feasibility and recruitment, including drafting of Site Information Questionnaires. Review assigned clinical documents for clarity and accuracy. Participate in the design and implementation of case report forms (CFRs), CRF and completion guidelines. Responsible for creation and update of Investigator Site Files from template supplied, including printing of required study documents. Review of data fields within the electronic data capture (EDC) systems, including performing and collating and downloading reports to support study management and data review | 1/26/2020 |
| 12623 | Principia Biopharma Emeryville, CA Software Quality Assurance Engineer BS/BA in technical field Exp: 1 year in customer hardware devices |
As a Medical Device Software Quality Assurance Engineer at Profusa you’ll work with small teams of hardware engineers, software engineers and scientists to make products that will truly improve human health. Develop test procedures to verify software and hardware according to subsystem requirements and execution sprints. Work with Hardware and Software Engineering, Design, and Product Management teams to identify high-impact issues | 1/26/2020 |
| 12624 | Progenity Ann Arbor, MI Quality Associate BS/BA Exp: 0-2 year in clinical molecular diagnostics lab |
The Quality Associate serves as a member of Progenity’s Quality Management team, whose focus is on supporting quality processes required by CLIA, CAP, NYS and other state and local requirements to ensure quality of patient test results in collaboration with the laboratory medicine and operations teams. | 1/26/2020 |
| 12625 | Progenity Ann Arbor, MI Research Associate BS or MS in life sciences Exp: 0-2 years |
The Research Associate is responsible for conducting experiments aimed at developing human genomics-based products for the NIPT, carrier screening, women’s health and human disease molecular diagnostics industries. Activities include developing experimental designs with supervisory input and carrying out well planned and controlled experiments. Data analysis activities are also practiced according to approved organizational standards followed by determination of future experimental and assay development activities resulting from such analyses. Experimentation will be aimed at implementation and optimization of technologies and completing the development and verification/validation of new Laboratory Developed Tests (LDTs). | 1/26/2020 |
| 12626 | Promega Madison, WI Custom Product Finishing Technician 1 HS Diploma/GED Exp: 2 year in product environment |
Work in a team environment to finish products to quality standards in order to meet custom production goals and productivity guidelines set by Promega. Fulfill customer requirements, meet and exceed customer expectations, to produce high quality, safe and effective products. This position will have a basic understanding of product finishing including process order execution, labeling, dispensing, and kitting. | 1/26/2020 |
| 12627 | Bio-Techne Woburn, MA Research Associate, Flow Cytometry BS/BA in biological sciences Exp: 0-2 years |
We are looking for an outstanding Research Associate to work in our Immunology Cell & Gene Therapy R&D group. This position will provide technical and logistical support for our R&D team with an emphasis on performing immunoassays to support our QuickGelTM related products. Use flow cytometry to perform experimental and quality control assays for characterization of products. Perform product development-related experiments under general supervision. | 1/26/2020 |
| 12628 | Bio-Techne San Jose, CA Manufacturing Laboratory Technician (Consumable--WES) AA Exp: 1+ year lab experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Operate and maintain robotic and manufacturing equipment. Ability to use hand tools such as small wrenches, pliers, tweezers, etc. | 1/26/2020 |
| 12629 | PCI Pharma Services Rockford, IL Entry Level Packaging Validation Analyst HS Diploma/GED Exp: 1-3 years experience or training |
The Validation Analyst I is responsible for overall validation project ownership of limited risk project(s) under heavy supervision. Responsible for generation and execution of validation protocols, assistance in audits, and determination of validation needs. This job has no supervisory responsibilities. | 1/25/2020 |
| 12630 | PCI Pharma Services Philadelphia, PA IT Helpdesk Technician AS/AA in related Exp: 1-3 years experience or training |
The role of the Helpdesk Technician is to assist customers with IT applications, products or services. Complex and/or high priority problems are elevated to specialized support groups for resolution however the HelpDesk Technician is responsible to ensure that an effective solution is provided to the user. Provides support for all Information Technology products and services. Support may include answering questions, troubleshooting problems, teaching or instructing customers regarding software or hardware functionality, and communicating policy. | 1/25/2020 |
| 12631 | PCI Pharma Services Rockford, IL Operations Process Engineer BS/BA in related Exp: 1-5 years |
This position will work to continuously improve processes and systems that ultimately lead to improved profitability to the company. Using all available Engineering, Lean and Six Sigma tools, this position will work independently and cross functionally to drive out waste and reduce process variability. Gather and analyze data using the operations data collection systems, including but not limited to: Overall Equipment Efficiency (OEE), uptime, scrap, margin, staffing, quality, capacity, safety and direct labor cost per unit to facilitate decision-making as well as identify and prioritize initiatives. This will require ownership of the data collection systems to insure the purity and consistency of the source. | 1/25/2020 |
| 12632 | PCI Synthesis Newburyport, MA Quality Control Analyst: 3rd shift Overnight BS in chemistry or related Exp: 1+ years |
The analyst is responsible for providing accurate and timely results for the samples submitted for analysis to support our manufacturing and research and development departments. Use liquid chromatography, gas chromatography, ultra violet spectroscopy, infrared spectroscopy, titrimetry, and other techniques to assess the quality of samples. The resulting data is interpreted by the analyst and submitted for review. The analyst is also responsible for ensuring that the instruments used for analysis are calibrated to industry standards. | 1/25/2020 |
| 12633 | PCI Synthesis Newburyport, MA Kilo Lab Chemist AS/AA in related Exp: 0-2 years, experience preferred |
PCI Synthesis is a leading manufacturer of Active Pharmaceutical Ingredients (APIs) and clinical drug substances. We are seeking a highly motivated, experienced Kilo Lab Research Scientist who would like to join our growing company. Proactive participation on project teams to guide R&D work prior to manufacturing runs • Preparation of Master Production Records (MPRs) based on lab procedures from R&D • Preparation of other regulatory documents • Active involvement in troubleshooting + investigations when problems are encountered. | 1/25/2020 |
| 12634 | PCI Synthesis Devens, MA Process Chemist R&D BS or MS in chemistry Exp: 0-5 years |
Highly productive, results-oriented individual, who will generate and implement original ideas and solutions that contribute to improvements in processes used to synthesize valuable compounds. Support drug substance process development via laboratory development, kilo lab scale-up. Prepare and characterize molecules using appropriate analytical tools including IR, NMR, MS, GC, and HPLC. | 1/25/2020 |
| 12635 | Pevalon na, FL Patient Sales Advocate BS/BA in related Exp: 1-3 years in medical field |
This is a Florida based Patient Sales Advocate position. Your position will be a blended position where you will work by phone calling patients and presenting The Eclipse solution as well as meeting with patients and medical practitioners in the field to educate and present the product. The ultimate goal of your phone calls is to convince the patient to schedule an appointment with a doctor to seek further information. The goal of your field work is to educate patients and practitioners on the benefits and use of the Eclipse solution. | 1/25/2020 |
| 12636 | Penumbra Alameda, CA Game QA Tester and Generalist HS Diploma/GED Exp: 1 year in gaming/software QA |
MVI Health is developing a revolutionary new product that uses state-of-the-art virtual reality technology to transform physical rehabilitation. As our QA Tester and Generalist, you will play a key role in ensuring quality in our product in order to deliver a great experience to our customers. If you are a fire-and-forget tester who can solve problems independently, and who wants to make a positive difference in people's lives, this position may be for you. | 1/25/2020 |
| 12637 | Penumbra Alameda, CA Quality Control Inspector HS Diploma/GED Exp: 1 year in QC inspection in med devices or similar |
As a Quality Control Inspector, you will test and inspect components and products in the laboratory. By ensuring that Penumbra's products meet the highest standards of quality and safety, you will play a key role in saving lives every day. Perform routine inspection at incoming Quality Control and finished device level. Inspect components, products, labels, boxes, pouches, and coatings visually and mechanically. Take measurements using micrometers, calipers, snap gages, gage pins and other measuring instruments. | 1/25/2020 |
| 12638 | Penumbra Alameda, CA R&D Engineer BS/BA or higher in mechanical/biomedical engineering Exp: 1-10 years |
As an R&D Engineer at Penumbra, you will be charged with designing game-changing medical devices to address some of the world’s toughest disease states. Design, prototype, and optimize meaningful medical devices that revolutionize treatment paradigms for a variety of challenging disease states. Create test protocols and conduct testing to mitigate clinical risk for a wide range of medical device concepts. Coordinate with suppliers and other external resources to source components and refine component specifications. | 1/25/2020 |
| 12639 | Penumbra Roseville, CA Quality Engineer BS/BA in engineering or sceicnes Exp: 1-5 years in biomedical/chemical/material engineering |
As a Quality Engineer at Penumbra, you will participate in all aspects of product manufacturing in order to ensure the highest level of quality in new and existing products, and their compliance to applicable regulations and standards. You will apply your passion for detailed analysis to identifying problems and determining the appropriate course of action. You will be looked to for ensuring compliance and building a culture of quality within your project teams. Represent Quality Engineering on process improvement projects, interfacing among multiple departments and teams such as Manufacturing, QC, R&D, Regulatory Affairs, Operations/Planning, and Marketing. | 1/25/2020 |
| 12640 | Performance Validation Multiple Locations, IN Level 1 Staff Validation Engineer / Specialist BS/BA in engineering or sceicnes Exp: Entry Level |
The Level 1 Validation Engineer/Specialist works within a small team environment to provide technical services to pharmaceutical or medical device manufacturers. Technical services may include interpreting drawings, manuals, or other technical information to develop requirement documents, developing testing documents that verify installation, and/or operation of the equipment, and execution /documentation of these testing documents. These documents are used by our life science customers to demonstrate compliance with USFDA regulations (or other regulatory bodies) for current Good Manufacturing Practices. | 1/25/2020 |
| 12641 | Perkin Elmber Waltham, MA Entry Level Consolidations Accountant BS/BA accounting or finance Exp: 0-2 years |
The Entry Level Consolidations Accountant will be an integral part of the Corporate Accounting team. The key areas of focus will be supporting the monthly close process, reviewing worldwide results and working with sites to make corrections, resolving accounting issues, and preparing global internal financial statements and financial data to support the consolidated external financials. This position also supports cross-functional finance teams across the organization through maintaining reliable financial reporting which requires an understanding of finance and accounting concepts as well as an aptitude for working with financial systems. | 1/25/2020 |
| 12642 | Perrigo Allegan, MI Associate Scientist / Scientist - Analytical R&D MS in chemistry or pharma sciences Exp: 1-2 years in cGMP/cGLP |
The Allegan Michigan based Analytical Research and Development department, specializing in solid and liquid Over-the-Counter (OTC) product development, is looking to add a talented colleague to our New Product Development team. Our focus is on the development of analytical methods for small molecules in support of research and characterization of new and reformulated drug products. Chief techniques include HPLC/UPLC-UV stability-indicating methods with various separation chemistries. Perform physical and chemical testing on raw materials, in-process and finished product samples with superior attention to detail and a focus on operational excellence. | 1/25/2020 |
| 12643 | Personalis Menlo Park, CA Laboratory Assistant (Temp to Perm) BS in molecular biology or related Exp: 0-2 years |
Within a dynamic startup environment, the successful candidate, under direction of the Laboratory management, will help grow the sequencing services laboratory. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. Adhere to the laboratory's quality control policies. Participate in laboratory support work as required by the team needs and at the direction of laboratory management. Lead the general upkeep, orderliness and cleanliness of the laboratory | 1/25/2020 |
| 12644 | Fc Performance Romeoville, IL Inside Sales Representative BS/BA Exp: 1-3 years in customer service |
Sell company products and services to customers by processing orders, price and delivery inquiries, providing technical and application information, soliciting customer orders and suggesting additional products in a fast paced multi-tasking environment. Processes and expedites orders, customer returns and returns to vendors in an accurate and timely manner. Locates product and creates purchase orders. Follows-up with vendors to ensure timely delivery. Works closely with Outside Salesman in soliciting business, executing order transactions and maintaining superior customer service levels. | 1/25/2020 |
| 12645 | Fc Performance Cleveland, OH Valve Technician HS Diploma/GED Exp: 1-3 years |
Mechanically and electrically troubleshoot, inspect, and test valves at specified job worksites. Primary worksites include FCX valve repair centers with occasional customer in-field work sites. Perform pre-testing, disassembly, cleaning, in process inspection, machining, lapping, painting, assembly, testing, and final inspection on various types of valves and actuation. Repair relief valves, control valves, on/off valves and pneumatic actuators in FCX actuation facility or customer plant locations. | 1/25/2020 |
| 12646 | Pii Pharmaceuticals Hunt Valley, MD QA Associate HS Diploma/GED, BS/BA preferred Exp: 1 year in QA |
To ensure the timely and accurate inspection of raw materials, in-process blends, and finished drug products while adhering to the cGMP and ICH guidelines as well as USP/NF/EP/JP/Health Canada, and other regulatory statues as written. To ensure that the day-to-day tasks of the Quality Assurance Unit supports the overall business plan while maintaining the highest quality drug products, ensuring the safety, identity, strength, purity, and quality that the drug is purported to possess. | 1/25/2020 |
| 12647 | Pii Pharmaceuticals Hunt Valley, MD Manufacturing Tech HS Diploma/GED Exp: 1-2 years in manufacturing |
Responsible for the mechanical setup, operation, control, monitoring and cleaning of various manufacturing equipment to produce solid dosage, semi-solid and liquid dosage forms following Standard Operating Procedures (SOPs). Performs assigned duties as outlined in the SOPs for manufacture of pharmaceutical products according to written instructions from Product Batch Records whilst following all safety requirements. To ensure that OPS services are compliant with the site’s quality standards, practices, procedures and documentation requirements and with site, local and federal safety requirements. | 1/25/2020 |
| 12648 | PharmaIN Bothell, WA Research Associate – Biology BS in biology Exp: 1+ years |
We are seeking a highly motivated Research Associate to support our growing Biology team. The successful candidate will enjoy working in a fast-paced environment, and have hands-on experience with laboratory maintenance, cell culture, ELISA, and laboratory rodent handling. | 1/25/2020 |
| 12649 | Pharm-Olam Houston, TX Clinical Trial Associate BS/BA Exp: 1 year as CTA II |
Acts as the primary administrative support to local Pharm-Olam clinical study teams, as required by Project Managers and Sponsors, thus ensuring that the clinical trial is conducted in accordance with international and local regulatory and ethic laws, ICH Guidelines for Good Clinical Practice and Standard Operating Procedures. Assists the local study team with the day-to-day conduct of international clinical studies. | 1/25/2020 |
| 12650 | Physical Science Inc Lanham, MD Contamination Control Engineer MS in chemistry, material science, physics or related Exp: 0-3 years |
Research Support Instruments is looking for a scientist/engineer with a broad range of experience for the development of optical space flight instrumentation. Contamination in the form of particulates, films, or scattered light can significantly degrade instrument performance and/or lifetime. Management of the cleanliness of optical and nearby surfaces throughout the lifecycle of assembly, integration, test, launch and operations requires a system approach. A successful contamination control engineer must work with designers and engineers throughout the entire process: design, process control, monitoring, cleaning, training, performance modeling, integration, and testing. | 1/25/2020 |
| 12651 | PhysIQ Chicago, IL Software Development Engineer in Test BS/BA or MS in technical field Exp: 1-3 years |
PhysIQ is looking for someone to join our growing team as a full-time employee in Test Engineering. This will involve testing new features, verifying bug fixes, and contributing to test automation across our front-end, back-end, mobile app, or api teams. This could involve Python, Java, Groovy, Kotlin, JS/TypeScript, WebDriver, Cucumber, or other technologies. | 1/25/2020 |
| 12652 | Platelet Biogenesis Watertown, MA Research Associate, Stem Cell Team BS or MS in biological sciences Exp: 0-2 years in lab/research setting with cell culture |
We are looking for a driven independent thinker with a monster work ethic who shares our long‐term vision for developing a source of donor-independent human platelets, and leveraging Mother Nature’s drug delivery system to cure diseases. Perform maintenance and differentiation cultures of human induced pluripotent stem cells, hematopoietic progenitors and megakaryocytes. Perform routine cellular and molecular biology procedures including but not limited to flow cytometry and microscopy | 1/25/2020 |
| 12653 | Aprecia Pharmaceuticals East Windsor, NJ Process Development Engineer BS in a technological field Exp: 1-2 year(s) |
This position typically works days, but responsibilities for this role may be covered across multiple shifts. Knowledge, Skills and Abilities: Solid knowledge of material characterization and process experience with pharmaceutical powder based solid oral formulations. Practical understanding of statistical control and software for data management and evaluation. Experience working with technical projects that span multi-functional teams. Excellent problem solving skills using team-based approach and known techniques for root cause analysis. Good writing skills for clear communication and accurate reporting. etc. | 1/21/2020 |
| 12654 | Aprecia Pharmaceuticals East Windsor, NJ Analytical Development Scientist MS in chemistry or related Exp: Not necessary for MS candidates |
This position is responsible for performing routine testing of raw materials, intermediates, and finished product to support product development. Works with minimal supervision to assist in analytical method development and pre-validation. Interacts extensively with Product Development and Quality functions to proactively deliver Analytical Development supports and to leverage analytical sciences to characterize and understand formulations and novel 3DP (three-dimensional printing) manufacturing processes. In addition, this position is also responsible for writing protocols, development reports, and SOPs (standard operating procedures); training others on analytical techniques; being familiar with USP/NF (United States Pharmacopeia/National Formulary) analytical procedures; and maintaining an understanding of cGMPs (current Good Manufacturing Practices) and ICH (International Conference on Harmonization) guidelines. etc. | 1/21/2020 |
| 12655 | Aptar Pharma Congers, NY Injection Molding Technician unspecified Exp: 1-3 year(s) |
Aptar Pharma is growing rapidly and has an exciting opportunity for a skilled Injection Molding Technician within in our Production team at our facility in Congers, New York. Aptar Pharma is part of Aptar Group, a global leader in the development and production of dispenser systems for the packaging industry. Aptar Pharma has been setting the standard for the drug delivery industry for decades and continue to break new ground providing innovative drug delivery devices, components and services, enabling the success of our clients. If you are eager for new challenges in Production in a fast-paced growing Company, we are the next step in your career! etc. | 1/21/2020 |
| 12656 | Aptar Pharma Congers, NY Quality Control Technician HS diploma or equivalent Exp: 1+ year(s) |
The Quality Control Technician performs dimensional and functional testing on Aptar Congers product to ensure compliance with established quality standards and customer specifications. The Quality Control Technician is responsible for documenting and communicating nonconformities to supervision. All Quality specifications, work instructions, as well as actions that support team work, safety, efficiency and cGMP adherence are to be followed. Primary Duties and Responsibilities: Perform incoming inspection and disposition of components. Perform analytical testing such as Spray Pattern testing, measurements, in-process and release testing as per the Quality specification. Initiate Discrepant Material Report for non -conformities. etc. | 1/21/2020 |
| 12657 | Evotec Watertown, MA Associate Scientist - ADME BS/MS in biology, chemistry, or pharmaceutical science Exp: BS: 1+ year(s), MS: 0-3 years |
The team seeks a scientist that is a highly motivated individual to performing a range of in vitro ADME assays (ex: solubility, microsomal stability, PPB, Cyp inhibition, Permeability) and PK studies to support the discovery and development of small molecule and peptide therapeutics. In this lab-based position, the qualified candidate will work closely with our established team to develop and conduct ADME assays to address ADME questions and support projects. The successful candidate would have the opportunity to interact with multidisciplinary project teams. | 1/21/2020 |
| 12658 | Evotec Rahway, NJ Lab Technician AS/BS Exp: BS: entry level, AS: 1-2 year(s) |
Evotec (US) Inc. has a Lab Technician position available, located at a compound management department at a Merck facility. The position entails following a specific set of guidelines to weigh, transfer and record chemical compounds. More specifically, the individual will prepare vials and tubes, place them in a chemical hood on an analytical balance, and transfer the vials or tubes using spatulas and pipettes and record the results. The balance will be connected to a computer that will collect the weights as they are measured. Responsible for services including but not limited to the day to day tasks of Screen File Build, as well as general compound management services including, but not limited to: robotics, validation, and overall laboratory maintenance. etc. | 1/21/2020 |
| 12659 | Evotec Princeton, NJ Research Associate MS in biological engineering or a biological science Exp: 1 year |
The candidate will join a cross-functional team responsible for profiling and production of recombinant proteins and assay ready cells for assays and biophysics. The applicant will be part of a team of up to 25 people in cell sciences, recombinant protein expression and purification from eukaryotic and prokaryotic hosts. Candidates will be responsible for the production, purification and/or characterization of a range of protein targets within the pharmaceutical arena. etc. | 1/21/2020 |
| 12660 | Archer Boulder, CO Software Engineer in Test I/II/III BS/BA Exp: 0-6+ years |
Software Engineers in Test build tools and test cases to verify software used in next-generation sequencing. They apply software engineering and computer science techniques to the unique problems of software testing. You will be working on a day to day basis with a team of software engineers and technical product managers defining and updating software requirements and design and translating them into automated tests. You will be responsible for writing, reviewing, updating regulated documents. As required, you will build test harnesses and other testing tools to accelerate testing. etc. | 1/21/2020 |
| 12661 | Archer Boulder, CO Regulatory Affairs Associate BS/BA Exp: 3-12 months |
The Regulatory Affairs Associate, reporting to the Regulatory Affairs Director, will help develop, implement and maintain the Regulatory Processes within the Quality Management System (QMS), including creation and maintenance of the documentation associated with filing for high risk medical device for the US and OUS submissions. RESPONSIBILITIES: Assist with the development and implementation of regulatory procedures. Assist in the communication with regulatory agencies. Support creation and manage filings for IDE, 510(k), PMA and EU Technical Files. etc. | 1/21/2020 |
| 12662 | Arcus Biosciences Hayward, CA Bioanalysis Research Associate BS/MS in chemistry, biochemistry, or related Exp: 1-4 year(s) |
Arcus Biosciences is seeking a highly motivated and team-oriented candidate for the position of Research Associate in the Drug Metabolism and Pharmocokinetics (DMPK) Department. The successful applicant will be responsible for performing bioanalysis of in vitro and in vivo samples to support discovery and development programs. Core responsibilities: Develop, troubleshoot, and validate LC-MS/MS based bioanalytical methods. Analyze, summarize and report preclinical pharmacokinetic and toxicokinetic results. Conduct in vitro ADME experiments such as metabolic stability, plasma protein binding, CYP inhibition and induction assay as necessary. etc. | 1/21/2020 |
| 12663 | Arcus Biosciences Hayward, CA Research Associate BS/MS in immunology, cell biology, biochemistry or related Exp: 1-2 year(s) |
Our Pharmacodynamics (PD) group is focused on the development and execution of assays to evaluate engagement of our drugs and their biological effects in patient samples. Our role within the Quantitative Biology (QB) department is a central, critical element of our translational research engine. We are looking to expand the size and scope of this team, with positions available immediately. The ideal candidate will have a working knowledge of immune-based in vitro assays, flow cytometry, ELISA, common molecular biology techniques, and data analysis/visualization software. Direct experience with isolation and culture of primary cells is strongly preferred. etc. | 1/21/2020 |
| 12664 | Argonaut Manufacturing Services Carlsbad, CA Drug Product Manufacturing Assistant HS diploma or equivalent Exp: 0-2 years |
The purpose of this position is to perform tasks and operations relevant to the bulk formulation and/or filling operations required for sterile production of liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing. General Responsibilities: Performs various routine manufacturing tasks under the direction of internal SOP’s and cGMP guidelines. Prepares material components for manufacturing operations. Documents steps clearly and completely in production batch records, log books and other controlled forms. Participates in inspection readiness activities. Performs basic arithmetic and algebraic computation. Maintain cleanliness of areas and equipment. etc. | 1/21/2020 |
| 12665 | Argonaut Manufacturing Services Carlsbad, CA Quality Control Assistant BS/BA in a life science Exp: 1-2 year(s) |
The purpose of this position is to provide support services by means of executing the analysis of in-process, finished product, and stability test samples. Further support services include Environmental Monitoring and Raw Material receipt activities. QC personnel are responsible for compliance with QC policies and procedures within the QC laboratory, company policies, and cGMP guidelines. This position will report to the Director, Quality Control. General Responsibilities: Directly contributes to daily laboratory operations for QC Chemistry and Microbiology, in full compliance with applicable SOPs and safety guidelines. Analyzes on a routine basis in-process, release, and stability test samples in accordance with established QC test methods and specifications. etc. | 1/21/2020 |
| 12666 | Arrakis Therapeutics Waltham, MA Research Associate, Target Biology and Translational Medicine BS in biology or related Exp: 1+ year(s) |
The mission of Arrakis Therapeutics is to extend small molecule medicines into new realms of biology by discovering and developing compounds that selectively target RNA (“rSM”). By targeting distinct RNA structure/function relationships, Arrakis is generating drug candidates with novel mechanisms of action for molecular targets that are challenging to drug in disease areas with high unmet medical need. As cell-based assay development and in-cell evaluation of high priority targets are critical to our mission, the Research Associate will make a major impact by assisting in the development and validation of new cell-based assays for high throughput screening. The Research Associate will also provide tissue culture support to aid critical projects, leveraging a broad array of tissue culture techniques, including cutting-edge techniques such as CRISPR editing. etc. | 1/21/2020 |
| 12667 | Arrakis Therapeutics Waltham, MA Research Associate, Molecular Biology BS in molecular biology, biochemistry, or biology Exp: 1+ year(s) |
The mission of Arrakis Therapeutics is to extend small molecule medicines into new realms of biology by discovering and developing compounds that selectively target RNA (“rSM”). By targeting distinct RNA structure/function relationships, Arrakis is generating drug candidates with novel mechanisms of action for molecular targets that are challenging to drug in disease areas with high unmet medical need. As Arrakis uses next generation sequencing (NGS) to enable the RNA structure and function assays that are central to our mission, the Research Associate will have an opportunity to make a large impact on our effort to establish world-class NGS methods and perform sequencing-based assays. etc. | 1/21/2020 |
| 12668 | Arraystar Rockville, MD Lab Assistant - Molecular Biology BS in a biological field Exp: 1-2 year(s) |
Responsibilities: Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 1/21/2020 |
| 12669 | Arrowhead Pharmaceuticals Madison, WI Research Technician BS in cell biology, molecular biology, biochemistry or related Exp: Entry level |
Arrowhead Research seeks a full time Research Technician to join its drug targeting team at its research and development facility in Madison, WI. The candidate should be highly motivated, and enjoy working with a team of scientists in a fast-paced and highly cross-disciplinary environment. The individual will be primarily responsible for providing technical assistance in RNA and DNA isolations, cell culture, and general laboratory maintenance. | 1/21/2020 |
| 12670 | Arrowhead Pharmaceuticals Madison, WI Scientist, Biology BS/MS in cell biology, molecular biology, or biochemistry Exp: 0-3 years |
Arrowhead is seeking a senior biologist to join our Research Department. The candidate will be a key member of drug discovery and development teams. S/He will be expected to: Design and execute/conduct in vitro or in vivo studies to facilitate drug discovery and development. Participate in new mechanistic studies. Present research findings to project teams and governance bodies and prepare technical reports. Maintain a high level of productivity in the lab and perform critical experiments. May mentor/supervise a team of one or more and guide and evaluate the performance of those individuals; is accountable for the effective performance of the team/individuals. | 1/21/2020 |
| 12671 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, Bioconjugation BS/MS in chemistry or biochemistry Exp: Entry level |
Arrowhead Pharmaceuticals is seeking an Associate Scientist to join the Chemistry Department. The successful candidate will primarily focus on bioconjugation, analytical chemistry, formulation, and some small molecule organic synthesis. S/He will be joining a team of highly motivated and experienced scientists, and will contribute to the success of Arrowhead programs. S/He will be expected to: Perform bioconjugation, purification, and characterization of oligonucleotide conjugates. Identify critical issues/steps in a conjugation and solve the problems in a timely fashion. Maintain a well-documented laboratory notebook. Track progress against project timelines, generate regular status updates, and communicate progress and issues to management. etc. | 1/21/2020 |
| 12672 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Discovery Analytical Chemistry BS/BA in chemistry or biology Exp: 1+ year(s) |
Arrowhead is seeking a highly motivated associate analytical chemist to join our growing Discovery Chemistry team. The successful candidate will be tasked with biological sample preparation and running HPLC to support ongoing discovery activities. S/He will be expected to: Follow the instructions to prepare samples from various biological matrix such as plasma, urine, tissues etc. Perform sample analysis using HPLC. Communicate on a timely basis with other functional groups. Generate regular status updates, and communicate progress and issues to management. Keep good documentation. Detail oriented and flexible for changes. Self-motivated team player with the ability to thrive in a fast paced, multi-disciplinary, matrixed environment. Maintain a high level of productivity in the lab and perform critical experiments. etc. | 1/21/2020 |
| 12673 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, CMC MS in chemistry or biochemistry Exp: Entry level |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Scientist to work as a Chemist in the Chemistry, Manufacturing, and Controls Group focusing on oligonucleotide synthesis development. This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates. The successful candidate will be expected to: Work closely with senior chemists on development of new synthetic approaches to desired compounds with an eye toward large-scale synthesis. Cooperate with other chemists in the group in preparation of complex organic constructs. Perform solid-phase synthesis and purification of oligonucleotide drug candidates. Analyze small-molecule and macromolecular targets using standard methods. etc. | 1/21/2020 |
| 12674 | AMRI Grafton, WI Quality Assurance Associate BS in chemistry or related Exp: 1-3 year(s) |
The Quality Assurance Associate is an integral part of the AMRI team, contributing to our success by assuring that all documentation, procedures and protocols comply with GMP and FDA guidelines. In this role, you will: Conduct batch record and test data reviews, and approve batches for release. Assist in maintaining compliance of Environmental Monitoring, Equipment Calibration, and the Equipment Maintenance Program. Issue Deviation, CAPA, and OOS investigations. Track investigations and outcome. Review and recommend approval of indicated actions to senior associates or quality management. etc. | 1/20/2020 |
| 12675 | ARL Bio Pharma Oklahoma City, OK Sample Administrator I / Receiving HS diploma or some college experience Exp: 0-2 years |
Occupations that fit well with this position are pharmacy technician and medical office administrative assistant. The job is performed in an office environment. This position is to perform all data entry processes needed or required to facilitate the accurate reporting of all samples submitted for testing. The Accessioner maintains sample integrity to ensure accurate and timely testing and reporting by the appropriate lab. Additionally, the Accessioner may perform additional duties requested by the Accessioning Supervisor. Minimal to moderate supervision is required. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. Marijuana is one of the substances included in the drug panel screening. etc. | 1/20/2020 |
| 12676 | ARL Bio Pharma Oklahoma City, OK Data Review Chemist I BS in chemistry or related Exp: 0-2 years |
With moderate guidance, the Data Review Chemist I is responsible for utilizing the Quality Management System (QMS) standard operating procedures (SOP) and work instructions (WI) to perform quality review and approval of test results and data for compliance. The Data Review Chemist I will independently apply technical aptitude and experience to troubleshoot non-compliant data and work supportively with other Chemists to ensure generation of compliant data. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. etc. | 1/20/2020 |
| 12677 | ARL Bio Pharma Oklahoma City, OK Research & Development Scientist I BS in chemistry or related Exp: 0-2 years |
The position requires the performance of variety of task including development and validation of analytical methods and qualitatively/quantitatively testing routine and non-routine client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation (HPLC/IC) used in a chemistry laboratory. Research Scientist I work with direct supervision and reports to the lab supervisor. The Research Scientist I must be able to think and work independently, yet share ideas and work toward team goals. Ability to express thoughts in a clear concise manner both orally and written is also expected. Works to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities. etc. | 1/20/2020 |
| 12678 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Microbiology Lab AS/BS in chemistry or related Exp: Not necessary for AS/BS candidates |
Under the supervision of the laboratory supervisor the Microbiology Lab Technician provides support tasks in a fast-paced laboratory setting. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. Marijuana is one of the substances included in the drug panel screening. Possession of a medical marijuana license will not excuse you from the testing process, or the consequences of testing positive for marijuana. etc. | 1/20/2020 |
| 12679 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Chemistry Lab AS/BS in microbiology or related Exp: Not necessary for AS/BS candidates |
This position is responsible for maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position is responsible for the daily calibration and/or verification of the balances and pH meter. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform limited tests under supervision. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. etc. | 1/20/2020 |
| 12680 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Analytical Lab AS/BS in microbiology or related Exp: Not necessary for AS/BS candidates |
Under general supervision, the Laboratory Technician is responsible for working collaboratively with Chemists and performing integral support tasks to ensure overall efficient testing of samples. Essential Functions: Adhere to Quality Management System (QMS). Follow prescribed safety rules and regulations in performing all assigned duties. Follow written and oral instruction. Prepare reagents, solutions, and mobile phases required for testing. Perform timely peer review of laboratory notebooks. Sample management including retrieval, storage, and disposal. Work and think independently, yet share ideas and work towards team goals. etc. | 1/20/2020 |
| 12681 | Angiodynamics Queensbury, NY Engineer I, Quality BS in engineering or related Exp: 0-5 years |
The Quality Engineer is responsible for assuring product quality through participation in cross-functional product development teams and by supporting manufacturing operations. Provide QE support for existing products and assist with the transfer of new products to production to drive continual improvement. Utilize quality tools to implement quality improvements, process mapping, process validations, software validations, production efficiency improvements, and process controls. Support product complaint failure investigations. Create and/or approve process validation protocols and reports. Initial corrective action reports as appropriate and investigates and implements corrective and preventive action plans. Participate with the material review board in determining the disposition of nonconforming materials. Design verification and validation strategy development and review and approval of validation and verification protocols and testing activities. etc. | 1/20/2020 |
| 12682 | ANGLE Toronto, ON Laboratory Manufacturing Associate HS diploma or equivalent Exp: 1-2 years |
The Manufacturing Associate works in a laboratory and clean room environment maintaining and operating standard laboratory equipment and executing routine manufacturing procedures following prescribed SOPs. Essential Duties and Responsibilities: Assembly of consumables in a clean room environment. Maintenance and operation of standard laboratory equipment such as centrifuges, pipettes, balances and pH meters. Receipt of incoming materials. Labelling and packaging manufactured products. Recording all data and results with accuracy and responsibility. etc. | 1/20/2020 |
| 12683 | ANI Pharmaceuticals Baudette, MN Contracts and Government Pricing Associate AS in finance, accounting, or related Exp: 1-2 years |
The Contracts and Government Pricing Associate assists in managing pricing for commercial contracts and assists in managing medicaid. Position Responsibilities: Pricing for Commercial Contracts: Direct support/backup for Contract Support Department. Contract Manufacturing; Wholesalers/Distributors; Retailers and Mass Merchandisers; Group Purchasing Organizations; and Buying Cooperatives. etc. | 1/20/2020 |
| 12684 | ANI Pharmaceuticals Baudette, MN Environmental, Health & Safety (EHS) Technician AS/BS in EHS, engineering, or a technical field Exp: 0-3 years |
The EHS Technician will support ANI’s Environmental, Health and Safety (EHS) program that provides for the occupational health and safety of ANI personnel, as well as compliance with environmental regulations at our facilities in Baudette, MN and Oakville, Ontario, Canada. Position Responsibilities: - Complete EHS program compliance support activities and procedure writing, as necessary. Maintain files and records pertaining to environmental, safety and industrial hygiene programs. Assist with the ANI Safety Committee activities. Coordinate and/or conduct site specific EHS trainings and activities (e.g. Lock Out/ Tag Out (LOTO) annual compliance tasks, incident investigation, ergonomics, respirator user clearance coordination, respirator fit testing, audiometric testing coordination, emergency action planning, hazard communication, lab safety inspections, etc.) and ensure these are documented appropriately. etc. | 1/20/2020 |
| 12685 | ANI Pharmaceuticals Baudette, MN Microbiologist BS in microbiology, biochemistry, or related Exp: Entry level |
This position is responsible for independently performing microbiological testing, as defined by governing standard operating procedures. This is an entry level professional position in the Quality Control Microbiology Laboratory. Position Responsibilities: - Perform microbiological testing on raw materials and finished product samples. Prepare standards, stock cultures, microbiological media and samples in accordance with approved methods. Identify microorganisms. Set-up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. Perform review of data collected under approved methods. Provide accurate assessments of data integrity, and document findings. Perform calibration, preventative maintenance and repairs as needed on instrumentation. Perform cGMP tasks such as laboratory housekeeping, auditing documentation, and maintenance of microbiology laboratory supplies. | 1/20/2020 |
| 12686 | ANI Pharmaceuticals Baudette, MN Operator I - Production HS diploma or equivalent Exp: 1-2 year(s) |
This position is responsible for operating pharmaceutical packaging machines/equipment. Position Responsibilities: Assists in material handling, equipment set-up and breakdowns, documents process according to Master Production Records, and works with trained operators at assigned work centers to learn all aspects of the position, including batch record documentation, equipment set-up, operation and clean up. | 1/20/2020 |
| 12687 | ANI Pharmaceuticals Baudette, MN QA Validation Technician HS diploma or equivalent Exp: 0-2 years |
This position is responsible for providing support to the Validation Department in execution of validation activities necessary to support department objectives and procedures. Position Responsibilities: Performance validation protocols to include but not limited to: Installation and Operation Qualification of Equipment, Process Validation and Qualification, Environmental Monitoring, Cleaning Validation swabbing. Coordination of required documentation in support of the validation packages: routing document for review and approval, coping / scanning / filing of documents. Preparation of sampling to include generation of sample labels and coordination of physical resources required to perform sampling. Audit of Validation protocol documentation to ensure that the information contained in the validation package is consistent with the supporting raw data. etc. | 1/20/2020 |
| 12688 | ANI Pharmaceuticals Baudette, MN QC Analyst BS in chemistry, pharmacy, or related Exp: Entry level |
This position is responsible for independently performing laboratory testing, as defined by governing test methods and standard operating procedures. This is an entry level professional position in the Quality Control Laboratory. Position Responsibilities: Perform testing on raw material, in-process, and finished product samples. Prepare standards and samples in accordance with approved methods. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. Perform review of data collected under approved test methods. Provide accurate assessments of data integrity, and document findings. etc. | 1/20/2020 |
| 12689 | ANI Pharmaceuticals Baudette, MN QC Technician HS diploma/AS/AA Exp: 0-5 years |
This position is responsible for support of QC testing activities. These responsibilities include: Position Responsibilities: Washing Laboratory Glassware. Sampling of Raw Materials. Inspection of Packaging Components. Minor Raw Material Testing. Filing of Laboratory Records and Documents. Special Project Assignments. Auditing Samples, Logbooks and Data Records. | 1/20/2020 |
| 12690 | Applied Medical Rancho Santa Margarita, CA Software Engineer - Web Developer (Full Stack) BS in computer science, computer engineering, or related Exp: 0-2 years |
The Applied Medical Simulation team was developed by Applied Medical as a result of the company’s founding purpose to improve patient outcomes through the delivery of affordable, accessible and high quality healthcare solutions. We maintain that surgical education, developed in close collaboration with the surgical community, is critical to advancing skills and improving clinical outcomes. As an Engineer I you will be responsible for working within the framework of a team and performing the following activities: Communicate with product experts, UI designers, and engineers to fully understand business requirements. Break down business requirements into clear and actionable tasks. Turn business requirements into clean, testable, and maintainable code. etc. | 1/20/2020 |
| 12691 | Applied Medical Rancho Santa Margarita, CA Production Associate - Assembly/Packaging (2nd shift) unspecified Exp: 1-2 year(s) |
As a Production Associate on 2nd shift, you will be responsible for working within the framework of a team in a cleanroom or manufacturing environment, and performing the following activities: Perform all manufacturing operations in a cleanroom or non-cleanroom environment such as assembly, inspection, and machine operations. Comply with Applied Medical Quality Systems (QS) including SOPs, MIs, QIs and TMs. Comply with safety and company policies. Comply with engineering drawings, shop order operations and sequence. Follow production schedules and meet production and quality goals. Perform manufacturing operations efficiently with or without tools and/or equipment. etc. | 1/20/2020 |
| 12692 | Applied Medical Rancho Santa Margarita, CA Production Associate - Assembly/Packaging (3rd shift) unspecified Exp: 1-2 year(s) |
As a Production Associate on 2nd shift, you will be responsible for working within the framework of a team in a cleanroom or manufacturing environment, and performing the following activities: Perform all manufacturing operations in a cleanroom or non-cleanroom environment such as assembly, inspection, and machine operations. Comply with Applied Medical Quality Systems (QS) including SOPs, MIs, QIs and TMs. Comply with safety and company policies. Comply with engineering drawings, shop order operations and sequence. Follow production schedules and meet production and quality goals. Perform manufacturing operations efficiently with or without tools and/or equipment. etc. | 1/20/2020 |
| 12693 | Paramit Morgan Hill, CA Functional Test Development Engineer I BS in EE, ME, or CS Exp: 0-2 years |
The effort involves following a test fixture development process that includes understanding the theory of operation of the UUT, architect/design fixtures, developing automation software GUI with a clear Pass/Fail indication and parametric record retention. Each project is unique and requires project management understanding like scheduling, working with customer as well as cross-functional team members to achieve the outcome at estimated cost, within lead time. | 1/20/2020 |
| 12694 | Parexel Billerica, MA Software Engineer BS in computer science, information systems, or related Exp: 0-3 years relevant experience |
Provide programming skills and expertise in the design and development of Enterprise Architecture projects: System Integrations, Analytical and Metrics Clinical Data Warehouse, Management of Production Release processes. Independently implement solutions following provided design blueprints, using established frameworks and design patterns, adhering to requirements, standards, and functional specifications. Responsible for unit testing of all code produced using preferred unit test frameworks and technologies | 1/20/2020 |
| 12695 | Parexel Billerica, MA Software Engineer BS in computer science, information systems, or related Exp: 0-3 years relevant experience |
Provide programming skills and expertise in the design and development of Enterprise Architecture projects: System Integrations, Analytical and Metrics Clinical Data Warehouse, Management of Production Release processes. Independently implement solutions following provided design blueprints, using established frameworks and design patterns, adhering to requirements, standards, and functional specifications. Responsible for unit testing of all code produced using preferred unit test frameworks and technologies | 1/20/2020 |
| 12696 | PBL Assay Sciences Piscataway , NJ Assay Services Scientist I/II BS/BA in life sciences Exp: 1+ year lab experience |
The Assay Services Scientist I / II works primarily with cell culture-based bioassays, executing antiviral bioassays, ELISAs and other highly sensitive immunoassays for characterizing proteins and reagents; analyzing data and drafting client reports; and developing new and custom assays to support the growth of the Assay Services Group. Execute immunoassays on ELISA, and other highly sensitive platforms like Electrochemiluminescence (MSD), Single Molecule Array (Simoa), and Single Molecule Counting (Erenna) | 1/20/2020 |
| 12697 | PBL Assay Sciences Piscataway , NJ Laboratory Technician BS/BA in biological sciences Exp: 0-3 years |
The Laboratory Technician is responsible for product manufacturing and ELISA kit optimization and stability testing following established guidelines and procedures and completing required documentation. The individual will routinely analyze raw data and generate summaries of work performed in compliance with Standard Operating Procedures (SOPs). | 1/20/2020 |
| 12698 | PBL Assay Sciences Piscataway , NJ Quality Control Scientist I BS/BA in biological sciences Exp: 1-2 years lab experience |
To ensure the quality of PBL reagents the Quality Control (QC) Scientist I will perform release and stability testing of interferons, antibodies, and manufactured ELISA kits. In addition, the QC Scientist I will perform bioassays or immunoassays to troubleshoot relevant customer issues and design and initiate experiments and projects to improve the quality of PBL products. The QC Scientist I may also serve as back up to the Product Development, Assay Services, or Manufacturing departments as needed: such additional duties may include designing and performing ELISA testing protocols, custom bioassays, and solution preparation. This individual will be involved with document control, SOP writing, and recordkeeping. | 1/20/2020 |
| 12699 | PBL Assay Sciences Piscataway , NJ R&D Scientist I/II/III MS in life sciences Exp: 0-2 years |
The R&D Scientist is responsible for the hands-on development of immunoassays, such as ELISAs and cell-based assays, for commercial production. This individual plans and executes design, development, and Manufacturing transfer of bioanalytical assays for product commercialization. The R&D Scientist is also responsible for development of custom assays and reagents for clients. | 1/20/2020 |
| 12700 | PBS Biotech Camarillo, CA Research Associate, BioprocessR&D (full-time) MS in chemical/biochemical engineering, or life sciences Exp: 0-2 years |
Participate in research efforts for various cell culture processes based on client needs. Perform experiments for bioprocess development, optimization, and characterization. Prepare scientific data for external publications, abstracts, and presentations, including those at international conferences and trade shows. Support root-cause analysis for unexpected results and provide new approaches or experimental strategies for problem solving. Characterize quality attributes of cells during process development, either independently or collaboratively with a customer’s analytical team or an external service provider. Support internal product improvement efforts by providing biological performance data using PBS products | 1/20/2020 |
| 12701 | PCI Pharma Services Rockford, IL Entry Level Packaging Validation Analyst HS Diploma/GED Exp: 1-3 years |
The Validation Analyst I is responsible for overall validation project ownership of limited risk project(s) under heavy supervision. Responsible for generation and execution of validation protocols, assistance in audits, and determination of validation needs. This job has no supervisory responsibilities. Prepares validation protocols, validation statements, reports, summaries, and master validation plans for new customer / product / system project launch and maintains existing validated processes / programs at multiple sites as well as organizing and coordinating internal and customer approvals, as needed | 1/20/2020 |
| 12702 | PCI Pharma Services Philadelphia, PA IT Helpdesk Technician AS/AA in related field Exp: 1-3 years |
The role of the Helpdesk Technician is to assist customers with IT applications, products or services. Complex and/or high priority problems are elevated to specialized support groups for resolution however the HelpDesk Technician is responsible to ensure that an effective solution is provided to the user. Provides support for all Information Technology products and services. Support may include answering questions, troubleshooting problems, teaching or instructing customers regarding software or hardware functionality, and communicating policy. | 1/20/2020 |
| 12703 | Pacific BioLabs Hercules, CA CLIENT SPECIALIST BS/BA Exp: 1 year in client facing role |
The Client Specialist (CS) is a full-time, on-site position to support testing department client account operations. This position will work closely with Pacific BioLabs Testing Department Heads and Business Development in ensuring that Client/Sponsor testing needs are met. The duties of the CS include 1) supporting the Client Account Manager in quote creation and quote follow-up and 2) department log-in and study file preparation. | 1/19/2020 |
| 12704 | Pact Pharma South San Francisco, CA Research Associate - Tumor Immunology MS in biological sciences Exp: 1+ year in immunology/immuno-oncology |
The person in this role will be responsible for performing immunological assays to functionally characterize the patient private NeoE-specific T cells, as part of product selection for the manufacture of the adoptive cell therapy product (neoTCR-P1). This process is performed in a GMP-like laboratory setting. The candidate should enjoy operating in an exceptionally dynamic and cooperative environment and will communicate results to and coordinate efforts with a larger cross-disciplinary team of immunologists, biologists, engineers and bio-informaticians. | 1/19/2020 |
| 12705 | Pact Pharma South San Francisco, CA Lab Automation Engineer BS or MS in engineering or sciences Exp: 1 year in lab |
he primary role is to interface with scientists to understand their workflows, and then develop automated solutions based on in house equipment or by identifying and bringing in the proper equipment/software solutions. More specifically the role requires scripting, testing and validating method and process development on Hamilton Vantage and Star liquid handling platforms, as well integrations with Agilent, Thermo, and other automation equipment. | 1/19/2020 |
| 12706 | Pact Pharma South San Francisco, CA Research Associate II - Gene Editing MS in molecular biology/immunology/virology Exp: 1+ year |
Responsibilities will include the generation of “next generation” DNA constructs utilizing various molecular cloning techniques. The incumbent will also be involved in the use of the DNA constructs and other genome editing tools to generate modified T cells for proof-of-concept experiments. This position will also be responsible for the proper analysis and documentation of studies, the presentation of findings, and assistance generating new SOPs. The incumbent will work closely with the Tumor Immunology group for the cellular analysis of product candidates, and may also assist with novel genetic analyses. | 1/19/2020 |
| 12707 | Pact Pharma South San Francisco, CA Research Associate - Clinical Immunology MS in cellbiology/immunology or related Exp: 1+ year in research |
Perform flow cytometry staining, sample acquisition, and analysis on clinical patient samples according to established standard operating procedures. Thoroughly document all work according to good documentation practices. Communicate clearly and concisely, both verbally and in the form of written reports. | 1/19/2020 |
| 12708 | Pact Pharma South San Francisco, CA Research Associate I or RA II - Tumor Immunology MS in biological sciences Exp: 1+ year in immunology/immuno-oncology |
We are currently recruiting for a Research Associate I or an RA II who will report to Scientist in Tumor Immunology and continue advancing PACT’s cutting edge engineered cell product. The candidate will perform and thoroughly document ex vivo T cell functional assays according to established procedures. She/he must have excellent organizational skills and should be able to communicate clearly and concisely, both verbally and in the form of written reports. She/he will aid in drafting new protocols, improving existing workflows, and provide data for regulatory filings to support clinical development. | 1/19/2020 |
| 12709 | Pall Syracuse, NY Engineer I BS in mechanical/material science engineering Exp: 0-5 years |
Looking for an enthusiastic team member to join Pall’s Inorganic Additive Manufacturing Team. Associate should be ready for hands-on engineering work in addition to working in a team environment. Duties: test stand set-up and evaluation; becoming subject matter expert on related processes; critical thinking and data analysis; creating 3D drawings; general lab duties | 1/19/2020 |
| 12710 | Pall Houston, TX Material Handler I HS Diploma/GED Exp: 1 year in distribution/warehouse |
Incumbents must possess basic material handling skills and must be willing to learn and continuously expand knowledge, skills and abilities required to support this large distribution center. Collaboration and assisting/training others in completing daily work is an expectation and is critical for the role. Read and understand Standard Operating Procedures. Learn and follow standard work for all areas within a Value Stream. | 1/19/2020 |
| 12711 | Pall Cortland, NY RDLP Associate MS in science or engineering Exp: 0 years |
During the two-year program, you will work alongside some of the brightest minds in the industry and will participate in four, six-month assignments engaging your technical and leadership skills. In these assignments you will experience at first hand many facets of R&D – project management and project team direction; process application studies, product design using tools like CAD or our proprietary in house filter design modules; prototype manufacture and testing; and product transfer to manufacturing. | 1/19/2020 |
| 12712 | Par Pharmaceutical Rochester, MI Chemist I BS in chemistry/chemical engineering Exp: 0-1 years |
The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. May participate in investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. | 1/19/2020 |
| 12713 | Par Pharmaceutical Chestnut Ridge, NY Manufacturing Operator l HS Diploma/GED Exp: 0-2 years |
The Manufacturing Operator I performs functions relating to the processing of drug products, ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements and in conjunction with all Standard Operating Procedures (SOPs). Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. Learns to apply skills and knowledge to recognize issues and to increase efficiency, throughput and quality. Learns, understands and runs processes to meet the assigned standards/routers and fulfills the assigned schedule; when these are not achieved, may participate in the debrief to understand the reasons why and what needs to be corrected moving forward. | 1/19/2020 |
| 12714 | Catalent Bloomington, IN Associate Scientist - Product Development MS in sciences Exp: 0-2 years |
This role will also work to develop a thorough understanding of the techniques, processes, and applications of technical knowledge to implement a process suitable for manufacturing of both drug substance (DS) and drug product (DP). A scientist in analytical development will be responsible for developing and executing analytical methods (ELISA, HPLC, Mass Spectrometry, Spectroscopic, Biophysical, etc.) for supporting process development activities. | 1/19/2020 |
| 12715 | Catalent Madison, WI Biomanufacturing Operations, Senior Associate MS/MA in biotechnology Exp: 0 years |
The Biomanufacturing Operations, Senior Associate position will independently perform batch record/date review, drafting technical documents protocols and reports. The Biomanufacturing Operations, Senior Associate will also be responsible for training/mentorship of junior staff and driving process improvement initiatives. You will work Wednesday through Saturday (4/10) on second shift and enjoy a shift premium. | 1/19/2020 |
| 12716 | Catalent Harmans, MD Quality Assurance Associate I BS in life sciences Exp: 1+ years |
Quality Associate I (QA Operations) is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product to be used for human consumption. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. Quality Associate I (QA Operations) is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product to be used for human consumption. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. | 1/19/2020 |
| 12717 | Catalent Madison, WI Associate, Quality Control BS/BA in biotechnololgy Exp: 0 years |
The Associate, Quality Control position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate is able to be trained on technical procedures and once trained, execute them consistently and reliably. Additionally, this position will support Preventative Maintenance and basic Laboratory maintenance activities while maintaining a GMP quality system. Other duties may include data review/archiving, database entry and contributions to process improvement initiatives. | 1/19/2020 |
| 12718 | Catalent Kansas City, MO Associate Scientist - Biologics BS/BA Exp: 0-3 years relevant experience |
In support of large molecule therapeutics, execute laboratory work plan / schedule developed with input from supervisor or senior team member. Sample types include in-process, release or stability. Analytical techniques may include any or all of the following: HPLC/UPLC techniques/methods (e.g. SEC, IEX, RP-HPLC, HIC, peptide map, glycan analysis, etc.). Karl Fischer, Compendia assays, (i.e. appearance pH, etc.). UV-Vis, Solo-VPE, Nano Drop | 1/19/2020 |
| 12719 | Catalent Harmans, MD Quality Control Analyst - Cell Culture AS in life sciences Exp: 1-4 years in GMP clean rooms |
Perform adherent and cell culture testing in a Phase III/Commercial GMP Manufacturing facility. Includes but is not limited to: thawing, enumeration, passaging and cryopreservation of various cell line types required for QC assays. Provide support to analytical/process development to onboard new client assays or enhancement to the testing capabilities of the cell culture laboratories. Provides input on SOP revisions and may assist in the creation and editing of protocols. Works closely with manufacturing and QA to coordinate cell culture activities required to support manufacturing operations and product release activities. | 1/19/2020 |
| 12720 | Catalent Harmans, MD Manufacturing Associate I AS/AA or BS/BA in engineering or biotechnology Exp: AA/AS: 0-2 years, BS/BA: 0-1 years |
The Manufacturing Associate I performs and documents cGMP activities to support upstream or downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed. The Manufacturing Associate I performs and documents cGMP activities to support upstream or downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed. | 1/19/2020 |
| 12721 | Paragon Genomics Hayward, CA Research Associate, Operations BS/BA in life sciences Exp: 1+ years in NGS lab, or entry level |
This is a laboratory-based position with great career potential for a junior scientist or technically oriented entry level candidates who already have or wishes to gain hands-on molecular biology experience in the next-generation sequencing space. This position offers a rare opportunity to build a strong multidisciplinary foundation in an exciting space. The ideal candidate must have good interpersonal and problem-solving skills. He/she should be driven to learn and motivated to develop great products and maintain the highest quality standards. | 1/19/2020 |
| 12722 | OriGene Rockville, MD Research Associate - Molecular Biology BS in life sciences Exp: 1+ year in DNA cloning/cell culture |
The qualified candidate will support company’smolecular biology operations,principally performing DNA cloning and molecular biology experiments following protocols. Perform experimentsfollowing protocols for plasmid DNA purification, DNA digestion, gel electrophoresis,DNA fragment purification, ligation, transformation, DNA quantitation,DNA sequencing,PCRand cell culture. | 1/18/2020 |
| 12723 | OriGene Rockville, MD ResearchAssociate, Protein Purification BS or MS in biological sciences Exp: 1+ year in DNA cloning/cell culture |
Research Associate in Protein Department: TheOriGene ProteinDepartmenthas been developing genome-wide purified recombinant proteinfrom human HEK293 cells, over-expressed lysates,Knockout (KO) cell lysates,cancer cell lines lysatesandheavy-labeled full-length protein.We are looking for individuals who would like to be a part of our Protein Department. Willingness to learn relevant molecular biology, transfection and hands on skills of various biochemical assays such as SDS-PAGE electrophoresis, BCA, ELISA. Western blot, recombinant protein purification | 1/18/2020 |
| 12724 | OriGene Rockville, MD Research Associate –Immunology BS in biology/biochemistry or life sciences Exp: 1-2 years in industry |
Involves multiple de novo R/D projects for antibodyand assay products development.Performsvalidation tests on variant sera or antibody samples. Participates other duties such as antibody production, purification and conjugation. Strong organizational skills and possess strong ability to identify, analyze and solve the problems independently. Records experiment procedure and results in notebooks and computer accurately. | 1/18/2020 |
| 12725 | Johnson & Johnson Eugene, OR Junior Sales Consultant (Trauma) – Eugene, OR BS/BA Exp: 0-3 years relevant experience |
Assist team in retaining and supporting further penetration with existing customers, while supporting product conversions with new customers. Assist in the attainment of established sales goals including market share objectives in prescribed territory. Apply knowledge of sales process, product portfolio and customer knowledge to improve sales outcomes. | 1/18/2020 |
| 12726 | Johnson & Johnson Malvern, PA Associate Scientist, Drug Product Development Engineer MS in related sciences Exp: 1 year lab experience |
The Associate Scientist, Drug Product Development Engineer in the Parenterals and Liquids (P & L) group will be responsible for performing experimental studies related to process improvement and quality compliance efforts as it relates to formulation/process development and testing of therapeutic proteins or other biologics including monoclonal antibodies (mAbs). This includes the mathematical modelling; and development and optimization of the technical operations associated with liquid and lyophilized biologics formulations/processes, as well as execution of pharmacy manual and stability studies. | 1/18/2020 |
| 12727 | Johnson & Johnson Malvern, PA Assistant Scientist BS or MS in biological sciences Exp: BS: 1-2 years, MS: 0 year |
The Assistant Scientist in the Parenterals and Liquids (P & L) group in Drug Product Development will be responsible for performing experimental studies as it relates to process development and testing of therapeutic proteins or other biologics including monoclonal antibodies (mAbs), virus like substances, cell-based therapeutics (CAR-T) and gene therapy related molecules. This includes the development and optimization of the technical operations associated with liquid and lyophilized biologics processes, as well as execution of stability studies. Additional responsibilities include but are not limited to development and optimization of liquid and lyophilized biologics formulations, as well as execution of characterization plans and stability studies | 1/18/2020 |
| 12728 | Bausch Health Lynchburg, VA Distribution Associate I (579) HS Diploma/GED Exp: 6 months distribution/warehouse experience |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, returns processing, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader. | 1/18/2020 |
| 12729 | Bausch Health Greenville, SC Distribution Associate (306) HS Diploma/GED Exp: 1 year distribution/warehouse experience |
Receiving operation is responsible for accurately receiving product from the B&L Manufacturing Operation along with other third party vendors, putting product into assigned storage locations, and retrieving product and delivering it to the pick area and/or shipping lanes. Also, perform shipping duties including preparing orders for shipment consisting of pallet stacking, labeling and wrapping. All order transaction controlled via RF computer. Shipping operation is responsible for accurately retrieving product from the pick area. Also, perform shipping duties including pallet stacking, labeling and wrapping. Other responsibilities include truck loading and general warehouse housekeeping. All order transaction controlled via RF computer. | 1/18/2020 |
| 12730 | Orthofix Remote, na Associate Territory Manager, PhysioStim - Philadelphia HS Diploma/GED Exp: 1 year sales experience (business to business) |
To assist Territory Manager in achieving sales results at or above established quotas for total and individual product segments. To provide direct, personal and timely service, via a consultative approach, to physicians, podiatrists, patients, managed care or other payors, representing Orthofix in a professional and straight forward manner. Additional responsibilities will include managing, directing, and assisting any authorized Orthofix distributor. Some shift in emphasis from calling on doctors to calling on payors is dictated by changes in the health care environment. | 1/18/2020 |
| 12731 | Orthofix Lewisville, KY Assembler I - BioStim HS Diploma/GED Exp: 1-2 years electrical assembly |
Perform basic electrical and mechanical assembly functions as defined by the Manufacturing Procedure. Must have the ability to meet or exceed all minimum departmental performance levels in the areas of Quality, Attendance and Productivity. Perform a wide range of electrical and mechanical assembly functions utilizing soldering and hand-eye coordination skills. Receive and comprehend formal documentation, safety, GMP, Workmanship and Hazardous Chemical Training. | 1/18/2020 |
| 12732 | Miltenyi Biotec Sunnyvale, CA Manufacturing Science and Technology Associate BS/BA in biological sciences Exp: 1-3 years in cell culture/clinical processing |
The unique duties of this position will consist of supporting the development of scalable cell culture processes as well as the manufacturing of primary human cells including activities that involve graft engineering for cellular therapies. Furthermore, you will be responsible for completing successful qualifications and material flow procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. This position will primarily involve routine GMP cell processing and facility/equipment support with research and development work on an as needed basis. | 1/18/2020 |
| 12733 | Miltenyi Biotec Gaithersburg, MD PD Associate I BS/BA Exp: 1+ year experience will cell culture/filtration/chromotography |
As a member of the Lentigen Technology Process Development team, you will have the exciting opportunity to support the development and tech transfer of processes to manufacture purified Lentiviral vectors used for pre-clinical and clinical products. You will apply your knowledge and prior laboratory experience to support the pre-clinical and clinical manufacturing of Lentiviral vector products. Familiarity with cell culture and/or purification technologies and analytical methods will enable you to assist in the development and tech transfer of processes compliant with GMP manufacturing requirements. | 1/18/2020 |
| 12734 | Miltenyi Biotec Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years in cell culture/clinical processing |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. | 1/18/2020 |
| 12735 | Miltenyi Biotec Gaithersburg, MD R&D Scientist, Purification & Characterization MS in molecular biology/immunology/virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to develop methods for the separation of different particle types and their characterization. Also, you will develop, evaluate and implement novel analytical methods for the fine characterization of viral vectors and exosomes, in view of the distinction of viral vectors from exosomes. You will design specific experiments to test LV function, perform statistical analysis of results, and communicate results internally, for use in publications, and in scientific meetings. Your responsibility will also include the development of chromatography-based separation steps in-view of the optimization of an existing purification protocol and their standard characterization. | 1/18/2020 |
| 12736 | Miltenyi Biotec Sunnyvale, CA Process Development Associate BS/BA in life sciences Exp: 0-2 years |
As a member of Miltenyi Biotec’s Process Development team, you will have the exciting opportunity to support the development of new processes that will generate cellular therapeutic products. You will apply your GLP/GMP experience to perform and maintain cell cultures using aseptic techniques. Ideally, you will be able to order materials and maintain inventory with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical cell and gene therapy products. In addition to your primary responsibilities, you will document activities for reproducibility, clean and maintain laboratory equipment and support team members as needed | 1/18/2020 |
| 12737 | Miltenyi Biotec Auburn, CA Accounting Associate AS/AA Exp: 1-3 years in corporate business/accounting |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. | 1/18/2020 |
| 12738 | Pace Analytical Golden Valley, MN Food Sample Handling HS Diploma/GED Exp: 0-3 years relevant experience |
The Sample Handling Lab Technician will work as part of a fast-paced sample prep team that organizes and processes materials for further analytical testing. Responsibilities include knowledge or use of various grinding mills and procedures for the preparation of samples for Analytical testing. Other responsibilities include filing, data entry, customer service and general lab upkeep (e.g. ordering and stocking supplies, cleaning, equipment maintenance) | 1/18/2020 |
| 12739 | Pace Analytical Maplewood, MN Complaint Analyst - Health Care BS/BA in biomedical sciences or pre-med Exp: 1+ years |
This candidate will manage and support complaint handling workflow for one or more client products. Assure appropriate prioritization and timely closure of complaints. Assure compliance with all FDA regulations and internal procedures related to complaint handling. Manage complaint handling workflow. Meet daily team and individual complaint handling output goals. Perform complaint investigation to either close the complaint or determine need for more in-depth analysis | 1/18/2020 |
| 12740 | Pace Analytical Maplewood, MN Lab Analyst - Mechanical Engineer BS in sciences/engineering Exp: 0-1 years in mechanical engineering |
This Lab Analyst will work in a product development lab to design and build hardware related to food safety equipment. Perform reliability testing and analysis related to hardware usage. Design and develop high level prototypes. Analyze data and create summary reports . | 1/18/2020 |
| 12741 | Pace Analytical Naperville, IL Lab Analyst - Chemical and Physical Testing AS/AA in applied sciences, BS in chemistry/biology preferred Exp: 0-2 years |
The main function of a laboratory technician is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. Set up and conduct chemical experiments, tests, and analyses using techniques such as chromatography, spectroscopy, physical and chemical separation techniques, and microscopy. Conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials | 1/18/2020 |
| 12742 | Pace Analytical Minneapolis, MN Quality Engineer Assistant BS in chemistry or related Exp: 1+ years in QA |
Candidate will work with Quality Assurance as a Quality Engineer Assistant to ensure compliance of manufacturing processes in a GMP environment. This person will serve as reviewer and/or approver for required documentation in a pilot plant/manufacturing setting. This position is very project orientated, so the QE Assistant can expect every day to be different with changing responsibilities and priorities. | 1/18/2020 |
| 12743 | Alcami Durham, NC Assistant Scientist II BS in pharmaceutical science, chemistry, or related Exp: 1-2 year(s) |
The Assistant Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Analytical Assistant Scientist II may also assist with method development/method validation projects. Typical types of testing: assays (potencies, related substances, residual solvents, metals etc.), rate of release (dissolution), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. etc. | 1/13/2020 |
| 12744 | Alcon Huntington, WV Production Technician HS diploma or equivalent Exp: None required |
The role of the Production Technician is to perform a number of different tasks and operations typically within a full-scale environment production manufacturing operation while maintaining compliance with Standard Operating Procedures, Good Documentation Practices and regulatory requirements. | 1/13/2020 |
| 12745 | Alcon Fort Worth, TX Scientist I BS/BA Exp: None required |
Job Description: Assist with in-vivo testing of raw materials, finished goods, products, investigations per schedule and per standards/SOPs. Collect, calculate, and interpret test results. Enter and report test results. Take ownership and execute revisions for SOPs related to testing programs, laboratory operations and/or equipment operation. Assist with investigative testing to support laboratory investigations. Conduct peer review of data collected by co-workers. Coordinate equipment calibration & maintenance. etc. | 1/13/2020 |
| 12746 | Alcon Fort Worth, TX Associate Scientist, Pre-Clinical Development BS in chemistry or related Exp: 0-1 year(s) |
Responsibilities: Follows established procedures, protocols, or best practices to analyze stability and development samples. Perform assigned tasks under minimal supervision in support of approved projects and documents work properly. Executes a well-designed study, conducts testing and analyzes data without deviation following established procedures under general supervision. Applies general technical skills to complete assigned work, and solves routine problems of limited scope. etc. | 1/13/2020 |
| 12747 | AliveCor Mountain View, CA Hardware Test Engineer BS in electrical engineering Exp: 1-5 year(s) |
AliveCor, the creator of the Kardia Mobile ECG app, seeks a Hardware Test Engineer to join an exciting start-up that is changing the face of mobile health. As the Hardware Test Engineer, you will be a crucial member of hardware R&D team responsible for ensuring that AliveCor products perform as intended and meet/exceed customer expectations. You will work closely with our Quality, Regulatory, Software Engineering, Product Management, and Creative teams to ensure new products perform as intended while fully documenting the verification process. You will also work with our manufacturing team to implement and support manufacturing test fixtures. If you have what it takes to drive change in the medical marketplace, then this is the opportunity for you. etc. | 1/13/2020 |
| 12748 | Alturas Analytics Moscow, ID Laboratory Assistant HS diploma Exp: 1-3 year(s) |
The Laboratory Assistant provides support to other laboratory personnel through a variety of duties and tasks. Essential Duties and Tasks: Maintains all lab supplies (including purchase, receipt, stock, inventory, and disposal). Prepares various reagents and solutions for laboratory use. Assists laboratory personnel to enable efficient laboratory operations. Performs routine facility maintenance and inspections. Cleans laboratory glassware. Additional Duties and Tasks: May perform QC review of data if needed. Performs other duties as needed or assigned. | 1/13/2020 |
| 12749 | APi North Augusta, SC MFG - Laboratory Technician HS diploma or equivalent Exp: Entry level |
The Laboratory Technician position is an entry level position. The person in this position will be trained and responsible for following instructions and procedures in support of manufacturing processes in a controlled GMP environment, as well as performing related activities. SPECIFIC DUTIES AND RESPONSIBILITIES: Must manage and organize the glass cleaning operation according to approved standard operating procedures. Works closely with Warehouse technician and Quality Assurance to perform and complete all Final Product packaging’s. Must manage time well. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. Follow approved GMP manufacturing directions such as standard operating procedures and other instructions in support of production. etc. | 1/13/2020 |
| 12750 | APi North Augusta, SC Purification Chemist BS in chemistry or related Exp: Entry level |
The Purification Chemist I position is an entry level chemist position. The person in this position will be trained and responsible for following the peptide manufacturing process in a controlled cGMP environment, as well as performing related activities. PRIMARY RESPONSIBILITIES: Work in a cGMP environment to perform the peptide purification processes through chromatography as well as other various purification techniques. Use analytical skills to prevent and solve possible process complications and problems. Work as part of a team to complete specific projects in a timely manner. Follow approved cGMP manufacturing directions such as production batch records, standard operation procedures and standard test procedures. Help the team to install, test, operate and maintain equipment for manufacturing and in-process testing. etc. | 1/13/2020 |
| 12751 | APi North Augusta, SC MFG - Laboratory Technician II HS diploma or equivalent Exp: 1-2 year(s) |
The Laboratory Technician II position is an experienced lab position. The person in this position will be trained and responsible for following instructions and procedures in support of manufacturing processes in a controlled GMP environment, as well as performing related activities. SPECIFIC DUTIES AND RESPONSIBILITIES: 1) Must manage and organize the glass cleaning operation according to approved standard operating procedures. 2) Works closely with Warehouse technician and Quality Assurance to perform and complete all Final Product packaging’s. 3) Must manage time well. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. etc. | 1/13/2020 |
| 12752 | APi North Augusta, SC Quality Control Chemist I BS in chemistry or related Exp: 1-2 year(s) |
Primary Responsibilities: Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Perform and review QC release testing. Support routine analytical testing using GC, KF, and HPLC. Assist the QC/QA group with writing and editing of SOPs and STPs. Support analytical method development. Perform method transfer and validation activities. Perform OQ/PQ for the Quality Control Equipment. Other duties as assigned. | 1/13/2020 |
| 12753 | American Regent New Albany, OH Maintenance Technician - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
American Regent, Inc., a Daiichi Sankyo Group Company, develops, manufactures, and supplies high quality sterile injectables for healthcare providers, clinics, hospitals and veterinary practices across the United States and Canada. We have locations in New York, Ohio, and Pennsylvania and sales territories nationwide. Nature and Scope: A technical position involving equipment repairs and maintenance activities intended to keep the facility equipment (i.e. process, utility, and general equipment) within compliance of cGMPs. etc. | 1/13/2020 |
| 12754 | American Regent New Albany, OH Metrology Technician I - 2nd Shift HS diploma/AS in electronics Exp: 1-5 year(s) |
NATURE AND SCOPE: A technical position involving instrument calibrations and operation intended to keep the facility instrumentation and equipment (i.e. process, utility, and general equipment) within compliance of cGMPs. ESSENTIAL DUTIES AND RESPONSIBILITIES: Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Perform Calibrations. Follow written calibration procedures. etc. | 1/13/2020 |
| 12755 | American Regent New Albany, OH Equipment & Process Technician I - 1st Shift HS diploma or equivalent Exp: 1+ year(s) |
The Equipment and Process Technician I works with the Inspection and Packaging Supervisor in the activities associated with the inspection and packaging of sterile pharmaceuticals in accordance with company procedures and cGMPs. The incumbent meets inspection and packaging schedules while maintaining accurate records and professional behavior within the inspection/packaging areas. The Technician will perform manual inspection and train in the automatic inspection/packaging area for setup, of automated equipment and manual inspection processes, labeling and packaging equipment duties, line clearances and assist with inspection/packaging schedule. In conjunction with the Supervisor, the Technician plays a critical role in assuring safe, effective and compliant activities are performed in the manual inspection process while maintaining production schedules. The Equipment and Process Technician I will be proficient in all activities associated with the inspection process and be able to work with minimal supervision. etc. | 1/13/2020 |
| 12756 | American Regent Hilliard, OH Component Prep Operator I - 2nd Shift HS diploma or equivalent Exp: 1 year |
This entry level position is a member of the Manufacturing Team. The Manufacturing Team is responsible for activities associated with the manufacture of safe, effective, and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Manufacturing Team ensures aseptic and sanitary conditions are maintained where required, that appropriate manufacturing area and equipment records are neat and accurate and that safe, effective and professional behavior is displayed at all times. In conjunction with Production Management the Manufacturing Team provides input and assistance to other Departments as needed, playing a critical role in maintaining production schedules and meeting Company Goals. The Team Member will be able to participate in all aspects of the Component Prep Process. The Component Prep Process includes dispensing components (Caps and Seals), vial washing and component sterilization in accordance with established production records in a concentrated effort to manufacture sterile liquid pharmaceuticals. etc. | 1/13/2020 |
| 12757 | Amneal Pharmaceuticals Piscataway, NJ Regulatory Affairs Associate BA/BS in a scientific field Exp: 0-2 years |
The Regulatory Affairs Associate supports the business and Regulatory Affairs team in day-to-day activities associated with the compilation and submission of regulatory submissions such as ANDAs to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws. Essential Functions: With some guidance compile and complete the ANDAs with high-quality, following the regulatory guidelines and internal processes within time lines. Coordinates with external vendors for project support activities. This may include but not limited to RS statements, TSE/BSE statements, Melamine free certificates, cGMP certificates, Debarment certificates, US agent letters, DMF LoAs, Technical data sheets, and technical drawings, Quantitative compositions of colors, flavors e.t.c. etc. | 1/13/2020 |
| 12758 | Amneal Pharmaceuticals Branchburg, NJ QA Inspector I - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
The Quality Assurance Inspector I monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector I must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run. Essential Functions: Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. etc. | 1/13/2020 |
| 12759 | Amneal Pharmaceuticals Brookhaven, NY Scientist I, Quality Control BA/BS in chemistry or related Exp: 0-1+ year(s) |
The Scientist I - QC is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. Essential Functions: Performs physical and chemical analysis of raw materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques adhering to company policies as identified in standard operating procedures (SOPs). etc. | 1/13/2020 |
| 12760 | Amneal Pharmaceuticals Brookhaven, NY Lab Technician I - 2nd Shift AS Exp: 0-1 year(s) |
The Lab Technician will be responsible for performing daily calibration of lab equipment, reports and maintain results. Essential Functions: Conduct daily calibration of instruments by utilizing small equipment like Balances, pH meters, Desiccators and Refrigerators. Login and maintain incoming samples for analysis in APR web. Prepare laboratory supply, chemical purchase request and maintain chemical inventory in APR web. Maintain column log books for HPL, GC and UPLC analysis. Dissolution media preparation and keep dissolution apparatus clean after each use by Scientist. Document reference standards and impurities in incoming material log book and update as needed. etc. | 1/13/2020 |
| 12761 | AMRI Grafton, WI Quality Control Analyst I BS in chemistry or other natural science Exp: 1-3 year(s) |
The Quality Control Analyst is an integral part of the AMRI team, contributing to our success by ensuring that our products meet all specifications before being released to the customer through raw material testing, method development, validation, equipment calibrations, environmental monitoring, stability testing and final product testing. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. etc. | 1/13/2020 |
| 12762 | AGC Biologics Bothell, WA Manufacturing Associate, Downstream BS in chemistry, biology, or related Exp: 1-8 year(s) |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. Complete required processing documentation including deviation reports, change control, product change over, etc. Ensure compliance with company quality systems, safety procedures, and other company policies. etc. | 1/12/2020 |
| 12763 | AGC Biologics Bothell, WA Manufacturing Associate I-IV BS in chemistry, biology, or related Exp: 1-8 year(s) |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. Complete required processing documentation including deviation reports, change control, product change over, etc. Ensure compliance with company quality systems, safety procedures, and other company policies. etc. | 1/12/2020 |
| 12764 | AGC Biologics Bothell, WA Manufacturing Associate I-IV, Team 2 BS in chemistry, biology, or related Exp: 1-8 year(s) |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. Complete required processing documentation including deviation reports, change control, product change over, etc. Ensure compliance with company quality systems, safety procedures, and other company policies. etc. | 1/12/2020 |
| 12765 | AGC Biologics Bothell, WA Manufacturing Support Technician I-IV BS in engineering or science Exp: 0-2 years |
The Manufacturing Support Technician is an entry level position for an individual to support the Technical Operations group. Primary responsibilities include generating and editing documentation in support of Process Transfer activities, helping manage equipment procurement and implementation, reviewing technical documentation, and providing general support to Manufacturing improvement initiatives. PRINCIPAL RESPONSIBILITIES: Work with the Technical Operations team to support the transfer of new processes into the Manufacturing operation. Key responsibilities include managing the creation of Manufacturing Batch Records, supporting development of Raw Material estimates, and helping to manage the closure of key equipment gaps. Support the implementation of new technology into the manufacturing operation. etc. | 1/12/2020 |
| 12766 | AGC Biologics Bothell, WA QC Associate I BS/BA Exp: 1-3 year(s) |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. PRINICIPAL RESPONSIBILITIES: Supports projects / initiatives / team goals by delivering on all assigned tasks. Analyzes issues and makes decisions based on standardized processes and procedures under direct supervision. Seeks opportunities for continual learning. Receives close and regular instruction, guidance and direction from others in the form of steps and tasks. Perform general QC testing such as pH, Osmolality, Protein Concentration. etc. | 1/12/2020 |
| 12767 | AGC Biologics Bothell, WA QC Associate I/II BS/BA Exp: 1-3 year(s) |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. PRINICIPAL RESPONSIBILITIES: Supports projects / initiatives / team goals by delivering on all assigned tasks. Analyzes issues and makes decisions based on standardized processes and procedures under direct supervision. Seeks opportunities for continual learning. Receives close and regular instruction, guidance and direction from others in the form of steps and tasks. Perform general QC testing such as pH, Osmolality, Protein Concentration. etc. | 1/12/2020 |
| 12768 | AGC Biologics Bothell, WA Development Associate I (Upstream) AA/BS in a life science or engineering field Exp: 0-3 years |
This is a Development Associates position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. PRINCIPAL RESPONSIBILITIES: Maintain lab including cleaning, autoclaving reactors, stocking laboratory supplies and performing maintenance on laboratory equipment. Prepare and filter media. etc. | 1/12/2020 |
| 12769 | Agilent Boulder, CO Manufacturing Quality Engineer - Entry BS/BA Exp: 1+ year(s) |
Ensures that high-quality products are designed, engineered and manufactured by Agilent, in conformance with required standards and regulations. This is a Quality position with direct support of manufacturing floor responsibilities. Provides guidance, expertise and services to ensure process, data and product quality. Participates in process improvement opportunities and provides quality-related services to quality control, R&D, manufacturing engineering, production, procurement, and others. etc. | 1/12/2020 |
| 12770 | Agilent Boulder, CO Manufacturing Tech (2nd Shift) unspecified Exp: None required |
Responsible for performing a variety of technical support duties in one or more manufacturing areas. Duties may be related to installation, maintenance, repair and support of manufacturing equipment, technical support of one or more production processes, product test and troubleshooting, and technical analyses and problem-solving. Conducts tests, experiments and/or problem resolution associated with components, parts, products or processes/systems. May design and/or build tools. etc. | 1/12/2020 |
| 12771 | Agilent Wilmington, DE Analytical Instruments Technical Support BS in chemistry, biology, or related Exp: None required |
As an Analytical Instruments Technical Support person, you will sit at our Agilent site in WIlmington, DE and join Agilent Technologies CrossLab Group's Online Technical Support Team. We support U.S. external customers. As an active team member, you will support customers requesting hardware, software and applications assistance with Analytical Products and Solutions and route those customers whom you can't help to the appropriate groups. Our group's organizational goal is that as part of a world-class technical support group, we provide insights to customers at their very first contact. In order to be successful, our response needs to be quick and well-informed. etc. | 1/12/2020 |
| 12772 | Agilent Wilmington, DE R&D Electrical Engineer BS/MS in electrical engineering Exp: None required |
As an Electrical Engineer in our R&D group, you'll be part of a team that analyze, design, prototype and test new products for Agilent's Gas Chromatograph, Automated Sample Handling and Automated Sample Preparation products. Most projects require mechanical, electrical and firmware engineers, as well as chemists and software engineers, to create a complete system. As part of those projects, you will also work with our marketing, manufacturing, purchasing and service organizations to transform your designs into shipping products. etc. | 1/12/2020 |
| 12773 | AGTC Gainesville, FL Research Assistant - Assay Development Preclinical Research & Development MS in a biological science Exp: Not required for MS candidates |
The Research Associate Assay Development Preclinical Research and Development is responsible for support of the Assay Development team by developing,qualifying and troubleshooting quantitative, semi-quantitative, and qualitative assays in support of research, nonclinical, and clinical programs. The Research Associate will report directly to the Supervisor, Assay Development Preclinical Research & Development. Develop and qualify new assay methods in support of IND enabling non-clinical animal studies, including in vitro cell-based assays, immunoassays, and molecular assays. Plan strategies for and participate in the development, qualification, and transfer of quantitative and semi-quantitative bioanalytical methods to support product release. May assist in preparing technology transfer, assay validation and clinical sample testing at CROs. etc. | 1/12/2020 |
| 12774 | AGTC Gainesville, FL QA Specialist I BS in a scientific background Exp: None required |
Essential Duties and Responsibilities: Support the development, implementation, and improvement of corporate quality systems that support early, mid and late phase gene therapy clinical programs. Increase compliance awareness and promote a culture of quality throughout the company, with a focus on laboratory and manufacturing operations. Collaborate with multiple functions to perform QA oversight and ensure quality-related activities are executed efficiently. Write, review and revise standard operating procedures. Provide training to laboratory and manufacturing staff on GLP/GMP regulations, best practices and internal requirements. Review and approve product-related documentation, including raw material release, batch records, quality control test results and resolve discrepancies, as needed. etc. | 1/12/2020 |
| 12775 | Ajinomoto Bio-Pharma Services San Diego, CA Aseptic Cleaning Technician HS diploma or equivalent Exp: 0-2 years |
Ajinomoto Bio-Pharma Services is currently seeking a Part Time Aseptic Cleaning Technician (3rd shift) responsible for formulating cleaning solutions and sanitizing manufacturing core, operation equipment, and monitoring production processes and operations as necessary. The Aseptic Cleaning Technician will record information in documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), and review documentation as appropriate. This role frequently works in a professional manufacturing environment with computer equipment, machinery, tools, and loud noise and activity. etc. | 1/12/2020 |
| 12776 | Ajinomoto Bio-Pharma Services San Diego, CA Document Control Assistant HS diploma or equivalent Exp: 0-2 years |
Ajinomoto Bio-Pharma Services is currently seeking a Document Control Assistant responsible for coordinating the review and approval of GMP documents using an electronic document management system. Responsibilities: Coordinates document changes within an electronic document management system. Issues batch records, laboratory notebooks, and logbooks for use in GMP production and testing activities. Collaborates with document authors and reviewers to process document changes within project timelines and in accordance with established procedures. Facilitates client review and approval of documents. Esures proper maintenance of document master copies and original production records. | 1/12/2020 |
| 12777 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Inspection Technician - 1st and 2nd Shift HS diploma or equivalent Exp: 0-2 years |
We are looking for multiple Drug Product Inspection Technicians for 1st and 2nd shifts. In this role you will be responsible for performing a wide variety of product inspection and packaging tasks. You will complete training and pass qualification testing for visual inspection of various product forms, perform accurate visual inspection and handling of products following SOPs while working under cGMP regulations. Please Note: 1st shift hours are 6:30 - 3:00 pm and 2nd shift hours are 3:00 - 11:30 pm. Responsibilities: Performs various manufacturing tasks under the guidelines of established SOP and cGMP regulations. Performs visual inspection. Labels and boxes filled goods. etc. | 1/12/2020 |
| 12778 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Assistant HS diploma or equivalent Exp: 0-2 years |
We are looking for multiple Drug Product Manufacturing Assistants for 1st Shift! The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. Responsibilities: Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Implements production and manufacturing procedures. Performs visual inspection. Prepares components, media, buffers, and other solutions as needed. Accurately documents data and completes batch records as needed. May cross train and/or focus in various manufacturing tasks including fill/finish, formulation, fermentation, preparation. etc. | 1/12/2020 |
| 12779 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Packaging Assistant HS diploma or equivalent Exp: 1-2 year(s) |
Ajinomoto Bio-Pharma Services is currently seeking a Drug Product Packaging Assistant. This position is responsible for performing a wide variety of packaging and labeling tasks in a GMP environment. In this role you will utilize automated equipment as well as perform manual packaging activities to support commercial drug product operations. Typical hours for this role are 7:00 to 3:30 pm Monday through Friday. Responsibilities: Performs various routine manufacturing tasks under the guidelines of established SOP and cGMP regulations. Performs final product assembly, packaging, and labeling and has completed required qualifications where applicable. Accurately documents data under cGMP guidelines. etc. | 1/12/2020 |
| 12780 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Substance Manufacturing Assistant - Support Services HS diploma or equivalent Exp: 0-2 years |
Ajinomoto Bio-Pharma Services is currently seeking a Drug Substance Manufacturing Assistant - Support Services responsible for performing solution formulation and/or sterilization of in-process manufacturing materials in support of cGMP manufacturing under the guidelines of established SOP's and cGMP regulations. Responsibilities: Transfers raw materials from warehouse staging area to production suite, labels materials for applicable client use. Conducts inventory and storage of raw materials in production area. Prepares components, buffers and other solutions and/or operates autoclave, washer, or depyrogenation oven. Completes in-process analytical testing as needed to confirm suitability of solutions and submits samples to QC for release testing via LIMS system. etc. | 1/12/2020 |
| 12781 | Ajinomoto Bio-Pharma Services San Diego, CA Environmental Monitoring Assistant HS diploma/BS in a life science Exp: 0-2 years |
We are looking for an Environmental Monitoring Assistant to support Ajinomoto Bio-Pharma Services’ manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. Responsibilities: Performs environmental monitoring within the microbiology laboratory, manufacturing suites, clean rooms, and drug product operations. Performs enumeration and gram staining of bacterial colonies. Sampling and analysis of the utilities including water, steam, and compressed gasses. etc. | 1/12/2020 |
| 12782 | Akorn Cranbury, NJ Analytical Scientist I BS in a chemical or life science Exp: 1-4 year(s) |
We seek talented Analytical Scientists at various levels to join our expanding R&D team. You will be responsible for methods and process development for ANDA topical, suspensions and solutions, nasal sprays, inhalations, sterile injectable and ophthalmic products. You will develop and validate new analytical methods, conduct stability studies and perform sample testing to support regulatory submissions. ESSENTIAL FUNCTIONS: Independently develop analytical methods for drug substances, drug product, preservatives and degradation/impurities in the new drug products. Perform validation experiments as per approved method validation protocols, Company SOP and ICH guidelines. Perform in-process, finished product/release and stability testing of dosage forms as per the approved methods. Perform Extractable/leachable studies for container closure systems of drug products. etc. | 1/12/2020 |
| 12783 | Novo Nordisk Clayton, NC Manufacturing Process Technician I HS Diploma/GED Exp: 1 year in manufacturing or BioWork Certification |
Operate manufacturing equipment to achieve production goals. Work in a safe and environmentally responsible manner. Assist during equipment maintenance including restoration of lost function, predictive and preventative maintenance. Reviewing and authoring standard operating procedures (SOP’s) and other documents as required | 1/11/2020 |
| 12784 | Novo Nordisk Clayton, NC API Manufacturing Associate BS/BA or higher Exp: 0-2 years in FDA regulated manufactruing industry |
Operate Active Pharmaceutical Ingredients (API) manufacturing equipment to achieve production goals. Work in a safe & environmentally responsible manner. Real time review of electronic batch records ensuring compliance to Standard Operating Procedures (SOPs) & current Good Manufacturing Practices (cGMP) standards. Utilize investigation skills during troubleshooting & assist during equipment maintenance, including restoration of lost function, predictive & preventative maintenance | 1/11/2020 |
| 12785 | Novum Las Vegas , NV Phlebotomist Phelbotomy certified Exp: 1-2 years |
The Phlebotomist will perform highly skilled, rapid-draw venipuncture and process collected biological samples according to Standard Operating Procedures (“SOPs”), sample collection and processing instructions; verify, pack and ship samples to appropriate facility. | 1/11/2020 |
| 12786 | Novum Las Vegas , NV Respiratory Therapist Respiratory therapy license Exp: 1 year in medical/research field |
The Respiratory Therapist will be responsible for performing all duties associated with respiratory function testing in accordance with Study Protocol and Standard Operating Procedures (SOPs). Responsible for performing and documenting respiratory function testing; observes dosing of study subjects to ensure appropriate respiratory function and compliance. Performs and documents drug devise training. Observes participant behavior during the study and will communicate pertinent observations and adverse events to the Study Manager or Investigator. | 1/11/2020 |
| 12787 | Novum Las Vegas , NV Screening Technician HS Diploma, training/experience in phlebotomy required Exp: 0-6 months |
The Technician in our Screening Department will be responsible for performing and assisting with screening activities according to study protocol and Standard Operating Procedures. Responsibilities include performing vital signs/measurements, EKGs, drug/pregnancy tests and other laboratory tests. Observes, obtains and processes all laboratory specimens required by the protocol. The Technician will perform quality control of lab results and charts prior to inclusion/exclusion to study. Performs service oriented duties in relation to participant needs, and provides general support to all phases of the screening process. | 1/11/2020 |
| 12788 | Novum Las Vegas , NV Research Technician (FT) HS Diploma/GED or 1-year cert from college/tech school Exp: 0-3 months |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 1/11/2020 |
| 12789 | Novum Las Vegas , NV Research Technician (PT) HS Diploma/GED or 1-year cert from college/tech school Exp: 0-3 months |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 1/11/2020 |
| 12790 | Novum Fargo, ND Entery Level Technician (PT) HS Diploma/GED or 1-year cert from college/tech school Exp: 0-3 months |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 1/11/2020 |
| 12791 | Nortech Bemidji, MN Assembler 1 - Bemidji (Day Shift HS Diploma/GED Exp: 0-1 month experience/training |
Duties include: Preforming basic assmebly tasts at a proficiency and quality standard rate set by the plant. Read/follow written build instructions (process sheets) to perform assigned operations. | 1/11/2020 |
| 12792 | Nortech Blue Earth, MN Quality Technician 1 year certificate from college/technical school Exp: 3-6 months related experience |
Coordinate the development/implementation of the quality systems, researching, developing and implementing the process improvements necessary to eliminate waste and reduce inventory. Responsible for development of the performance metric system used to report on continuous process improvements | 1/11/2020 |
| 12793 | Nortech Merrifield, MN Inspector 1 HS Diploma/GED Exp: 1-3 months related |
Newly hired and/or fully trained in one or more areas of quality. Works under close supervision on assignments that are routine in nature where limited judgement is required and typically detailed instructions on work are given. Examines compnay records to secure such information as size and weight of the product and results of quality test. Inspects produc to determine compliance with order specifications. | 1/11/2020 |
| 12794 | Nortech Blue Earth, MN Manufacturing Engineer BS in mechanical/manufacturing engineering Exp: 0-4 years |
Develops manufacturing methods, systems and processes; provides product support to engineering and manufacturing teams; resolves engineering problems; evaluates manufacturing system applications and equipment; confirms systems and components capabilities; develops manufacturing processes and stardards... | 1/11/2020 |
| 12795 | Nortech Maple Grove, MN Staff Accountant BS/BA Exp: 1 year experience |
Works independently with general supervision and works on assignments of moderate scope where judgement is required in resolving problems and making recommendations. Will exercise judgement within defined procedures and practices to determine appropriate action, and normally recieves general instructions on routine work and detailed instructions on new assignments. | 1/11/2020 |
| 12796 | Nortech Blue Earth, MN Assembler 1 - Blue Earth HS Diploma/GED Exp: 0-1 month experience/training |
Duties include: Preforming basic assmebly tasts at a proficiency and quality standard rate set by the plant. Read/follow written build instructions (process sheets) to perform assigned operations. | 1/11/2020 |
| 12797 | Nortech Blue Earth, MN Quality Technician 2 AA or 2 year degree Exp: 6-12 months related experience/training |
Works under general supervision on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Normally recieves general instructions on routine work and detailed instructions on new assignments. Performs internal audits for processes and products to assure compliance to the documented quality system. | 1/11/2020 |
| 12798 | NuVasive West Carrolton, OH Production Associate - 2nd shift HS Diploma/GED Exp: 0-1 years |
The Associate Post Processing Technician is responsible for the finishing/assembly operations to ensure quality products are produced. The Post Processing Technician helps in driving best practices and creates open communication across all teams to foster a collaborative, high functioning culture. Follow standard applications in order to achieve dimensional integrity and required finish characteristics. Follow the router protocol to ensure the product moves through channels efficiently and GDP is correct prior to moving the product to the next area. | 1/11/2020 |
| 12799 | NuVasive West Carrolton, OH Associate Quality Engineer BS in engineering Exp: 0-2 years in regulated quality environment/engineering |
This role is responsible for the, implementation, and improvement of overall quality systems. The Associate Quality Engineer will participate in Design Control activities and provide guidance to engineering on successful creation and maintenance of design history files during new product introductions. The Associate Quality Engineer may work closely with suppliers or contractors, including auditing, developing inspection/testing plans, performing risk analysis. | 1/11/2020 |
| 12800 | nView Medical Salt Lake City, UT Software Developer BS or MS in computer science/engineering Exp: 1+ years in design |
High throughput data processing and management. Algorithm development and optimization. Algorithm parallelization via General Purpose GPU computing. Computer vision, image creation, and image processing. Eliminating defects in our code and refactoring it to reduce its length, complexity and time required to test or add functionality | 1/11/2020 |
| 12801 | NxStage Medical Lawrence, MA Quality Analyst - NxStage BS/BA Exp: 0-3 years in related |
The incumbent will be responsible for receiving and processing customer product complaints in Fresenius/NxStage’s postmarket surveillance department with a primary focus on performing functions in support of the quality engineering and clinical teams. Process incoming customer complaints and adverse events as assigned for device and drug-related incidents. Interface with distributor contacts and customer clinical staff to obtain detailed information regarding reported incidents as required, ensuring patient confidentiality throughout | 1/11/2020 |
| 12802 | Ofni Systems Raleigh, NC Computer Systems Validation Engineer BS in math/science/engineering Exp: 1 year in software testing |
We are hiring a Validation Engineer to be on the cutting edge of automated validation techniques. You will be responsible for implementing our validation solutions while working with industry-leading companies. Ideal candidates are experts on the requirements of 21 CFR 11, have excellent critical thinking and interpersonal skills, and are motivated to meet client needs for compliance. If you are an A-level engineer who enjoys the challenge of solving real-world compliance problems then we would like to talk with you. | 1/11/2020 |
| 12803 | Ology Bioservices Alachua, FL QC Support Tech II AAS/AS in sciences Exp: 1 year experience |
Support of QC Laboratories including, but not limited to: Work with the procurement department to order reagents, materials, services and equipment for QC. Maintain inventories of materials for the QC departments. Perform equipment/laboratory cleaning and routine maintenance tasks. Responsible for washing and maintaining glassware. | 1/11/2020 |
| 12804 | Ology Bioservices Alachua, FL Assistant Scientist, Cell Assay BS in biological sciences or related Exp: 1-2 years performing tests in cGMP envi |
The Assistant Scientist, Cell Assay, reports to the Cell Assay Manager and performs QC laboratory tests on in-process, intermediate and finished products performing a range of additional varied work activities including: Assist in routine organization and upkeep of the laboratory, including maintenance of inventory, cleaning, and waste disposal. Writing and updating laboratory documentation including equipment SOPs and test methods. Performing routine immunoassays, cell-based assays, molecular biology assays and virology testing in support of product release, in-process testing as appropriate. | 1/11/2020 |
| 12805 | Ology Bioservices Alachua, FL Supplier QA Technician AA/AS Exp: 0-2 years in FDA-regulated industry |
Write standard operating procedures, work instructions, forms, material specifications, deviations, CAPA's, change controls and other relevant GMP records. Perform sampling, inspection and release of incoming material. Perform sampling and inspection intermediate and final product. Assess supplier quality performance | 1/11/2020 |
| 12806 | Ology Bioservices Alachua, FL QA Associate HS Diploma/GED Exp: 1 year in biologics/pharma industry |
The QA Associate is responsible for providing clerical and administrative support related to documentation. The QA Associate reports to the Kimberley Planter and will be responsible for activities related to generation and maintenance of documentation, including but not limited to: Converting the format of documents to match the template format. Assisting employees with document preparation including formatting and pagination. Assisting with progression of documents through Document Control Lifecycle in MasterControl | 1/11/2020 |
| 12807 | Olympus San Jose, CA Regulatory Affairs Analyst II BS in sciences Exp: 0-3 years in related |
The Regulatory Affairs Analyst II maintains responsibility for the review and investigation of medical device complaints. He/ she coordinates the resolution of complaints and ensures that timely investigations are performed. The incumbent prepares and files Medical Device Report (MDR) for Medical Systems Group(MSG) products. The incumbent maintains quality documents to ensure compliance with FDA regulations and guidance documents relating to these areas of responsibility. He/ she functions as part of MSGs Regulatory Affairs team in fulfilment of corporate objectives for FDA regulatory compliance. The Regulatory Affairs Analyst II performs routine assignments with occasional direction from supervisor;requires general instruction for new or special assignments from Supervisor and/or more experienced staff. | 1/11/2020 |
| 12808 | Olympus Southborough, MA R&D Engineer II MS in engineering, biomedical preferred Exp: 0 years |
As an Engineer II working on the R&D team, you will be empowered and inspired to do your best work. You will contribute to our mission by developing Surgical Platforms used primarily in Ear Nose and Throat surgery. In a typical day, you will develop hand held surgical instruments both and instrument consoles on your own and in conjunction with outside and inside design partners. The designs will require creative design solutions and component designs that are innovative and effective in meeting the needs of our customers | 1/11/2020 |
| 12809 | Olympus Richmond Hill, On Endoscope Technician I HS Diploma/GED Exp: 0-1 years in technical repairs |
The Endoscope Technician must understand and accept the responsibility to ensure the safety of all Olympus products that are repaired by strictly following established processes and procedures. Under the direction of the Manager, the incumbent shall evaluate, troubleshoot, disassemble, assemble, repair and inspect Endoscopes, Electronics, or Microscopy products to meet company product standards and ensure full and proper functioning of the repaired product. Level I Technician: Assignments are semi-routine difficulty level. Requires daily supervision, detailed instruction on new assignments. | 1/11/2020 |
| 12810 | Olympus State College, PA Assembler I HS Diploma/GED Exp: 0-1 years |
Electronic Assembler I is an entry-level assembler position performing a wide variety of mechanical assembly operations. Follows methods and sequence of operations in assembling cables, soldering, bonding, limited testing and manufacturing of transducers. Ability to follow procedures and drawings. | 1/11/2020 |
| 12811 | Olympus New Brunswick, NJ Field Service Engineer I AS/AA in electronics, computer science, or related Exp: 1 year as field service engineer or equivalent |
As a Field Service Engineer, the incumbent will engage with some of the country’s most influential hospitals and work closely with our world-class sales teams. He/ She will use your in-depth knowledge of our products to provide expert technical support to our existing and new customers. Perform new equipment installations, upgrades, post installation testing, troubleshooting and all other aspects of technical support for all assigned products. Build and maintain relationships of trust with customers by responding to inquiries and complying with all regulatory and quality requirements. | 1/11/2020 |
| 12812 | Olympus Center Valley, PA Technical Support Engineer I AS/AA in related field Exp: 1 year |
As a Technical Support Engineer I working on the Technical Assistance Center team, you will be empowered and inspired to do your best work. You will contribute to our mission by assisting customers with technical issues, researching complex problems, and striving for customer satisfaction. In a typical day, you will: Answer inbound customer calls make outbound calls as necessary. Investigate and resolve issues problems concerning all Medical products and update incident tickets and enter information in department database to permit generation of accurate reports regarding frequency of incidents and costs of repairs. | 1/11/2020 |
| 12813 | ThermoFisher Scientific West Hills, CA Scientist I, Manufacturing Sciences BS in biological sciences or related Exp: 1-2 years biological lab experience |
The Scientist I, Manufacturing Sciences is responsible for understanding, performing daily testing, and analysis for development and, improvement of DNA-based diagnostic reagents. Simultaneously manage and prioritize multiple projects and products across multiple functional groups while meeting target due dates with guidance of supervisor/lead. Design, create experimental task, run tests and be able to look at data and complete analysis using Fusion, Orchid, or equivalent software. Can provide experimental task(s) to designated Scientist with Supervisor approval. | 1/11/2020 |
| 12814 | ThermoFisher Scientific St. Louis, MO Formulation Technician II HS Diploma/GED or Associates Exp: 1-2 years in related |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) biopharmaceutical manufacturing, with a primary focus on Harvest and Media Preparation. | 1/11/2020 |
| 12815 | ThermoFisher Scientific Cambridge, MA Specialist I, Quality Assurance BS/BA in sciences Exp: 0-2 years in quality |
The Quality Assurance Specialist will be the primary point of contact for the customer on all matters related Quality Assurance Operations. Perform activities in support of dispositioning product and/or raw materials while ensuring compliance with directives and procedures, customer requirements, and regulatory standards. | 1/11/2020 |
| 12816 | ThermoFisher Scientific Suwanee, GA Lab Tech II BS/BA Exp: 1-3 years |
The Lab Technician II performs sample handling, receipt, storage, and shipment for a biorepository as well as entering inventory information into a laboratory information management system. Additionally, he/she performs specialized services including sample manipulation, aliquoting, and other sample handling functions that may require aseptic technique. | 1/11/2020 |
| 12817 | ThermoFisher Scientific Alachua, FL QA Specialist, GMP Plant Quality BS/BA in life or chemical sciences Exp: 1+ years in GMP environment |
Ensures the quality of all GMP manufacturing activities, executing manufacturing record reviews in accordance with specified timelines. Performs robust master and executed batch review and disposition activities to meet specified timelines. Performs robust document review and approval activities to meet specified timelines and ensure the adherence to Quality Agreements. Documentation may include batch records, SOPs, investigations, corrective actions, change controls, technical documents, | 1/11/2020 |
| 12818 | ThermoFisher Scientific Allentown, PA Associate Project Engineer BS in mechanical/industrial engineering Exp: 0-3 years in related |
The individual will establish a solid focus on long-term continuous improvement activities through interaction with the entire Engineering and Operations Staff.Recommend methods for improving worker efficiency, reducing waste, and utilities such as restructuring job duties, reorganizing workflow, relocating workstations, equipment, and justify and oversee purchase of new equipment / technology.Recommend and lead cost saving initiatives as it relates to business objectives, current projects, future investments in technology and Production / Manufacturing processes.Will lead and manage multiple project engineering driven assignments from start to finish with sound project management methodologies | 1/11/2020 |
| 12819 | ThermoFisher Scientific Lenexa, KS Customer Service Representative I HS Diploma/GED Exp: 1+ years in call center/customer service |
Employee is responsible for entering order into the MBD-Lenexa ERP system and assisting our internal and external customers with resolution of customer service issues and complaints. Enter orders as they are received via fax, email and/or phone as assigned by management; perform quality verification of customer shipping information, order details, and pricing. | 1/11/2020 |
| 12820 | ORA Andover, MA Clinical Trial Associate - Medical Devices BS in nursing or life sciences Exp: 1 or more years in clinical trials |
Assists project managers in clinical study conduct for ophthalmic clinical projects across all investigator sites and ensures compliance with protocol and overall clinical objectives. As a member of the clinical team, relies on instructions and pre-established SOP’s to perform the functions of the job while working under immediate supervision of a supervisor or manager. Performs day-to-day activities under the guidance of the project managers. | 1/11/2020 |
| 12821 | Organogenesis Norwood, MA QC Analyst I/II - Microbiology BS/BA Exp: 6-12 months in GMP/Medical devices/Pharma |
The QC Analyst I/II performs quality activities in support of product production and releases. The position has interaction with other internal departments, including Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also has interactions with external entities including contractors and suppliers. The QC Analyst I/II performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, and reporting results. | 1/11/2020 |
| 12822 | Organogenesis Norwood, MA Production Associate I - Human Tissue Processing Certificate in biotechnology preferred but not required Exp: 1-3 years |
The Human Tissue Processing (HTP) Production Associate I is an entry level position. The HTP Production Associate I will perform the production activities associated with HTP Products, produced at Organogenesis Norwood, with supervision. The associate will adhere to the appropriate SOPs, MBRs, and cGMP procedures in the general lab area as well as the Class 10,000 clean room. The HTP Production Associate I will report to the HTP Supervisor. | 1/11/2020 |
| 12823 | Acella Pharmaceuticals Indianapolis, IN Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. etc. | 1/7/2020 |
| 12824 | Acella Pharmaceuticals Portland, OR Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. etc. | 1/7/2020 |
| 12825 | Acella Pharmaceuticals Seattle, WA Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. etc. | 1/7/2020 |
| 12826 | ACIST Medical Systems Eden Prairie, MN Quality Engineer BS in engineering or related Exp: 0-5 years |
Provide hands-on quality engineering technical support for to the development of new medical devices, as well as changes to existing commercialized devices. This will include development of quality requirements/plans for new products, design/process validation requirements, test method validation and ongoing change management for finished device manufacturing. The Product Quality Engineer plays an active role in the processes to ensure product changes meet quality standards consistent with ACIST Medical Systems policies, while meeting all applicable regulatory requirements. The role works upstream and downstream ensuring the total product lifecycle is maintained and that our products continue to perform as designed. etc. | 1/7/2020 |
| 12827 | Acumed Nashville, TN Associate Sales Representative BS/BA in a business or medical discipline Exp: 0-2 years |
The Associate Sales Representative (ASR) exceeds sales quota within an assigned territory by delivering Acumed product on time and providing high quality technical assistance in the OR. The ASR assists in the assessment of the customer base to identify new business opportunities and executes a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 1/7/2020 |
| 12828 | Acumed Hillsboro, OR Regulatory Associate BS in a science, health, or technical discipline Exp: 0-2 years |
The Regulatory Associate supports the overall regulatory function by helping to maintain regulatory processes and systems. S/he utilizes computer and software proficiencies to create, coordinate, procure and/or maintain data and documentation to support US and OUS medical device registration. The Regulatory Associate also employs an attention to detail and developing familiarity with products and processes to ensure databases, dashboards and documents are current and correct. etc. | 1/7/2020 |
| 12829 | Acumed Danville, PA Sales Associate BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 1/7/2020 |
| 12830 | Acumed New York, NY Sales Associate BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 1/7/2020 |
| 12831 | Acumed Boston, MA Sales Associate BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 1/7/2020 |
| 12832 | Acumed Wichita, KS Sales Representative BS/BA in a business or medical discipline Exp: 0-2 years |
The Sales Representative (SR) exceeds sales quota within an assigned territory by delivering Acumed product on time providing high quality technical assistance in the OR and assists in driving market acceptance and adoption of Acumed Products utilizing technical and surgical knowledge. The SR assists continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 1/7/2020 |
| 12833 | Acumed Nashville, TN Sales Representative BS/BA in a business or medical discipline Exp: 0-2 years |
The Sales Representative (SR) exceeds sales quota within an assigned territory by delivering Acumed product on time providing high quality technical assistance in the OR and assists in driving market acceptance and adoption of Acumed Products utilizing technical and surgical knowledge. The SR assists continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 1/7/2020 |
| 12834 | Adaptimmune Philadelphia, PA Manufacturing Cell Therapy Specialist (2nd Shift) BS in cell biology, bioengineering, or medical technology Exp: 1+ year(s) |
RESPONSIBILITIES: Performs cell manufacturing related activities while wearing clean room attire in an aseptic cGMP manner. Documents production operations in corresponding batch records and log books per established procedures ensuring accuracy and timely completion. Identifies real time manufacturing issues (deviations and atypical results) and communicates them to the Manufacturing Manager and the Quality team in a timely manner. Responsible for drafting or modifying manufacturing documents with the Manager and Quality Team oversight. etc. | 1/7/2020 |
| 12835 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I-IV BS in medical technology or a physical or biological science Exp: 1-2 years |
The Production Associate position will be responsible for processing client samples using high throughput DNA sequencing technology. This role will work within a team of other Laboratory Technicians in a fast-paced, high production setting to process research and clinical diagnostic samples. The shift for this job is 7am-4pm, Sunday's through Thursday's. Responsibilities: Perform DNA/RNA extractions, PCR amplification and high-throughput sequencing assays on DNA libraries. Perform QC and carry out routine tasks accurately and following strict methodologies. Completes assignments of complex nature requiring a basic knowledge of techniques and practices related to the research area. Supports business goals, knowledge and skills, and cross-functional teamwork. Keep accurate and detailed records for all workflows. Ability to work independently and carry out optimization and validation experiments. etc. | 1/7/2020 |
| 12836 | Adaptive Biotechnologies Seattle, WA Study Management Specialist III BS/BA in biology or related Exp: 1+ year(s) |
The Study Management Specialist II is responsible for ensuring that incoming clinical trial and research projects are appropriately entered into laboratory information systems (LIMS) to ensure data integrity and conformance to project requirements prior to release of samples to the production laboratory operation. Job Responsibilities: Work cross functionally with computational biology and business development teams to generate data definitions and maps for incoming samples as defined in data transfer agreements. Ensure data definitions can be mapped to corresponding laboratory information management system (LIMS) fields, and hence ensure that data can be entered in a systematic manner. Prepare manifests that ensure consistency of data entry, and hence data integrity. etc. | 1/7/2020 |
| 12837 | Adare Pharmaceuticals Vandalia, OH Operator I HS diploma or equivalent Exp: 1+ year(s) |
Scope: Learning to disassemble, clean and reassemble production equipment to prepare for processing. Learning to conduct pre-processing staging to assure that required raw materials are assembled, weighed, and meets specified consistency as outlined in written procedures. Learning to operate the process equipment to create product that meets predetermined specifications. Learning to monitor and record critical process parameters. Learning to make necessary adjustments to assure finished product meets customer specifications. Learning to transfer processed materials through production equipment to include dryers, filtration systems, blenders, and sieving equipment. Learning to package finished product and transfer to warehouse. Learning to operate solvent recovery system to assure cyclohexane ingredient is of the purest form. etc. | 1/7/2020 |
| 12838 | Admera Health South Plainfield, NJ Associate Bioinformatics Scientist, Clinical Services MS in bioinformatics Exp: 0-2 years |
Responsibilities: Work collaboratively with bench scientists, comprehend project objectives, provide informatics solutions. Develop and implement bioinformatics analyses, applications, and workflows to expand our genomics and bioinformatics capabilities. Integrate computational analysis to project design and data interpretations. Maintain and improve back end of cloud-based genomic interpretation system. etc. | 1/7/2020 |
| 12839 | Admera Health South Plainfield, NJ Senior Clinical Technician BS in medical technology or life sciences Exp: 1+ years |
Responsibilities: Perform high complexity laboratory tests in accordance with SOPs and CLIA/CAP regulations. Evaluate and interpret results. Maintain accurate documentation and records (accessioning through result reporting). Proper handling of clinical samples. Maintain and operate lab equipment and instruments. Order supplies and reagents. Additional tasks may be assigned. etc. | 1/7/2020 |
| 12840 | Aesculap Allentown, PA General Manufacturing Associate (Detailed Assembler) 3rd Shift - Pain Control HS diploma or equivalent Exp: 0-1 years |
This position is to assemble, package and inspect medical devices in accordance with the quality and production standards established by our organization. This includes working with chemicals, machines and measurement equipment. This position must follow procedures, policies and applicable regulatory policies to meet the requirements of our Quality Policy. Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organizations products according to specifications and schedules; volume, cost and waste targets; quality standards. etc. | 1/7/2020 |
| 12841 | Aesculap Allentown, PA General Manufacturing Associate (Detailed Assembler) 2nd Shift - Pain Control HS diploma or equivalent Exp: 0-1 years |
This position is to assemble, package and inspect medical devices in accordance with the quality and production standards established by our organization. This includes working with chemicals, machines and measurement equipment. This position must follow procedures, policies and applicable regulatory policies to meet the requirements of our Quality Policy. Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organizations products according to specifications and schedules; volume, cost and waste targets; quality standards. etc. | 1/7/2020 |
| 12842 | Xeris Pharmaceuticals Chicago, IL Legal & HR Associate BS/BA Exp: 0-2 years |
The Legal & HR Associate is a key role responsible for supporting the Legal and Human Resources teams in an administrative capacity, working with employees across multiple states in the USA. The Legal & HR Associate is the face of Legal and Human Resources, interacting with and supporting all employees. The ideal candidate is ambitious, high energy and excited to get their foot in the door of an innovative company. This is a fantastic opportunity for someone interested in the legal or human resources functions within a company. etc. | 1/6/2020 |
| 12843 | ZeteoTech Sykesville, MD Chemist BS in chemistry or related Exp: 1-5 years |
Zeteo Tech, Inc, a venture backed company developing solution for Medical and Biodefense applications, is seeking a motivated chemist to join our team. The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your expertise to conduct chemical and physical laboratory tests to assist scientists in development of tools to detect and identify biological organisms and materials. etc. | 1/6/2020 |
| 12844 | ZeteoTech Sykesville, MD Microbiologist BS in microbiology, biology, biochemistry, or related Exp: 1-5 years |
Zeteo Tech, Inc, a venture backed company developing solution for Medical and Biodefense applications, is seeking a motivated microbiologist to join our team. The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your expertise to conduct biological laboratory tests to assist scientists in development of tools to detect and decontaminate biological organisms and materials. This is an entry-level position with room for growth. | 1/6/2020 |
| 12845 | Zoetis Durham, NC Associate, Research & Diagnostic Services BS in microbiology or other life sciences Exp: 1-2 years |
The U.S. Poultry Research & Diagnostics Services team provides diagnostics, research and development, outcomes research, and biodevice support through theoretical and applied scientific evaluations. The Associate is primarily responsible for assay testing; ARC (Avian Research Center) study implementation and reporting; meta analysis to inform health decisions and process interventions; day-to-day operations of the diagnostics laboratory (e.g., supplies, budget management, etc.); and assisting the Sr. Associate with duties as needed. In addition, the Associate is the primary commercial leads for the Laboratory Information Management Software (LIMS) system, providing superior service to internal colleagues and customers. etc. | 1/6/2020 |
| 12846 | Zoetis Parsippany, NJ Associate/Sr. Associate, Business Integration BS/BA in business, computer science, or related Exp: 1-5 years |
The Associate/Sr. Associate, Business Integration is responsible for helping to implement and execute the organization’s business integration objectives. The Associate/Sr. Associate will partner cross-functionally to build and execute the Zoetis integration strategy by assisting the Director, Business Integration in project management, change management, and process improvement initiatives. etc. | 1/6/2020 |
| 12847 | 10X Genomics Pleasanton, CA Production Associate 1 BS/MS in molecular biology, chemical engineering, analytical chemistry or related Exp: 1+ years |
10x Genomics is looking for an outstanding individual to join its consumable manufacturing team. This individual will be responsible for production consumable products associated with Next Generation Sequencing chemistries. This role requires excellent laboratory skills in performing production operations consistently. The ideal candidate will have an education background in one or more of the following disciplines: Molecular Biology, Analytical Chemistry, Chemical Engineering, or equivalent. Experience in production and QC of similar products in a manufacturing environment a plus. etc. | 1/6/2020 |
| 12848 | 10X Genomics Pleasanton, CA QC Associate 1 BS in chemical or biological engineering, molecular biology, or analytical chemistry Exp: 0-2 years |
10x Genomics is looking for an outstanding individual to join its Quality Control team. This person will be responsible for the qualification of consumable products associated with Next Generation Sequencing chemistries. As well as ensuring a reliable supply of quality consumables, this person will be a key contributor to the development of manufacturing infrastructure required to support a commercial product in the life science field. etc. | 1/6/2020 |
| 12849 | 10X Genomics Pleasanton, CA Computational Biologist – Microscopy MS in computer science, electrical engineering, mathematics or related Exp: 1-5 years |
10x is looking for an outstanding individual to join its Computational Biology group to work on its next generation spatial genomics assays. The ideal candidate has experience implementing robust algorithms for detecting and modeling features in microscopy images and drawing inferences from them. Candidate should have deep knowledge of optical image analysis and will be well served by the ability to combine published algorithms with original ideas and quickly turning it into efficient code. Candidate will be expected to be highly independent, relied on for their expert technical opinion and thrive in a quickly changing environment. etc. | 1/6/2020 |
| 12850 | 3M Charlotte, NC Manufacturing Associate HS diploma or equivalent Exp: 1+ year(s) |
Primary Responsibilities include but are not limited to the following: Follow standard operating procedures to assemble, test and package products. Follow all job safety recommendations. Enter data into ERP systems. Experienced in the use of hand tools, powered tools including routers, sanders, dremmel tools and measuring devices. Must be able to work with minimal supervision but also to take direction from team members in a small but highly motivated manufacturing team. Must have excellent housekeeping skills and be able to work with a very sticky Epoxy adhesive and 2-propanl without causing contamination of product, tools and equipment. etc. | 1/6/2020 |
| 12851 | AbbVie South San Francisco, CA Associate I/Associate II, In Vivo Pharmacology BS/MS Exp: 0-3 years |
We are looking for an Associate Scientist I/II with experience in in vivo pharmacology study execution, start to finish including tumor implantation, data collection, and data analyses. Additional opportunities to learn new skills and to work on ex vivo lab experiments will be provided based on project need and candidate’s interest. The ideal candidate will have experience working with various mouse models of cancer. Above all, we are looking for a highly motivated and collaborative individual with a passion for oncology research, who enjoys working in a fast-paced and highly dynamic working environment. etc. | 1/6/2020 |
| 12852 | AbbVie Lake County, IL Writer I & II, Development Document BS/BA Exp: 1-2 years |
The Development Document Writer I is accountable for authoring Development's quality documents by leveraging knowledge and expertise in writing standards and working with stakeholders to ensure the end to end processes are well-defined and articulated clearly in alignment with AbbVie's quality document system. Responsible for ensuring quality document standards are applied when authoring new and updating Development's quality documents. Responsible for understanding AbbVie's Quality System and applying the knowledge when authoring new and updated Development's quality documents. Provides internal stakeholders with the understanding of AbbVie Quality System and its practical application. etc. | 1/6/2020 |
| 12853 | AbbVie Worcester, MA Manufacturing Technician 2nd Shift BS/BA Exp: 0+ years |
Responsibilities: Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 1/6/2020 |
| 12854 | Abcam Branford, CT Senior Research Associate BS/MS in molecular biology or related Exp: 1-3 years |
The successful candidate will play a hands-on role in the company’s use of a variety of molecular biology, assay development, and protein purification techniques in support of various commercial and academic customer projects to deliver high-quality and on-time customized recombinant antibodies. He or she will partner closely with other team members within the group and be required to make observations, analyze data, and interpret results with supervision. etc. | 1/6/2020 |
| 12855 | Abcam Eugene, OR Research Associate (temporary) BS in biology, immunology, or related Exp: 1+ year(s) |
We are seeking a Research Associate to assist in the development of novel immunoassays in our Eugene, OR facility. The core responsibility will be to provide support to the immunoassay development team through the use of antibody-based laboratory techniques such as sandwich ELISA, Western blot, immunocytochemistry, and flow cytometry as well as the generation of biological materials for analysis. etc. | 1/6/2020 |
| 12856 | AbSci Vancouver, WA Research Associate - Fermentation BS in chemical or biochemical engineering, microbiology, or related Exp: 1-2 years |
The Fermentation Research Associate will play a significant role in our upstream process development. Core responsibilities include executing bench-scale fermentations with the goal of achieving high cell densities and maximizing yields of recombinantly expressed proteins. This position will be responsible for independently operating bioreactors at small scale (1L or less), preparing media, processing samples, and analyzing results. Candidate is enthusiastic about laboratory bench work, exhibits meticulous attention to detail, and an eagerness to learn new techniques. etc. | 1/6/2020 |
| 12857 | Absorption Systems Exton, PA Associate Scientist – Cell & Molecular Biologist BS/MS in biochemistry, molecular biology or related Exp: 0-2 years |
Absorption Systems provides analytical support for gene and cell therapy products through every stage of development and non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. Absorption Systems is headquartered in Exton, PA. Currently we are seeking a talented and highly motivated Associate Scientist – cell and molecular biologist in Exton, PA to contribute to multiple bioassay development projects. etc. | 1/6/2020 |
| 12858 | Absorption Systems Exton, PA Associate Scientist / Scientist – GMP Molecular Biology & Gene Expression BS/MS Exp: 1-3 years |
Primary Responsibilities: Conduct GMP study projects: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. Conduct studies on molecular biology assays, such as qPCR assays. Prepare and maintain cell cultures and reagents. Document all results in GMP laboratory notebooks and present research data in group and other meetings. Write report for the study project under the direction of management. | 1/6/2020 |
| 12859 | Absorption Systems Exton, PA Associate Scientist / Scientist – Drug Transport & Metabolism BS/MS Exp: 1-3 years |
Absorption Systems provides analytical support for gene and cell therapy products through every stage of development. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. Absorption Systems is seeking a candidate for either an Associate Scientist or Scientist position with drug transport and metabolism experience at the headquarter location in Exton, Pennsylvania. etc. | 1/6/2020 |
| 12860 | Accelerate Diagnostics Tucson, AZ Research Associate, Quality Control BS in chemistry, molecular biology, or related Exp: 1+ year(s) |
The Research Associate for Quality Control (QC) is a key member of the Operations Team under the direction of the Team Lead for Consumable Quality Control. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, HPLC-MS, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. etc. | 1/6/2020 |
| 12861 | Accelerate Diagnostics Tucson, AZ Research Associate BS in microbiology or related Exp: 1+ year(s) |
The Research Associate is a member of the Core Lab Team and help bring the company's innovative clinical microbiology technology to market. The ideal candidate will be a motivated self-starter with experience in the following areas: microbiology, biochemistry, and/or molecular biology. The successful candidate will be responsible for the day-to-day execution of experiments supporting assay development. etc. | 1/6/2020 |
| 12862 | Acceleron Pharma Cambridge, MA Facilities Technician AS/AA Exp: Not necessary for Associate degree candidates |
The Facilities Technician will handle multiple duties and daily activities as well as drive Facilities operations to meet deadlines in support of activities including, but not limited to, operation and maintenance of building systems, inventory management, conducting routine inspections, safety compliance, vendor management, and basic manual labor. etc. | 1/6/2020 |
| 12863 | Nobel Life Sciences Woodbine , MD Study Coordinator BS/BA in sciences Exp: 1 year related work |
Assist Study Director in determining staffing requirements, scheduling and documenting all critical events. Assist Study Director with protocols and reports preparation. | 1/6/2020 |
| 12864 | Nobel Life Sciences Woodbine , MD Quality Control Associate BS/BA in sciences Exp: 1 year in QC position |
Responsibilities include: Supervise day to day quality control operations and documentation. Assist in writing and reviewing SOPs, study protocols and reports. Coordinate in-house and external routine maintenance including calibration and certification and maintenance of lab equipment. etc. | 1/6/2020 |
| 12865 | Nobel Life Sciences Woodbine , MD Animal Lab Tech BS/BA in sciences Exp: 1 year in GLP, preferred |
Follow and perform standard operating procedures (SOP) & Protocols on study and stock animals, including, but not limited to: clinical observations, food consumptions, body weights, urine collection, administering anesthesia, mating procedures, blood draws dose administration, restraint, euthanasia, catheter placement, feeding, food removal, on laboratory animals. | 1/6/2020 |
| 12866 | Nobel Life Sciences Woodbine , MD Animal Care Tech BS/BA in sciences Exp: 1 year in GLP, preferred |
Read, understand and follow all SOP’s, Quality Assurance Standards and perform duties in accordance with the study protocol. Monitor daily animal health and wellness checks and report any abnormal animal conditions to the supervisor and/or the Study Director and record observations in appropriate log. | 1/6/2020 |
| 12867 | Nordson Minneapolis, MN NPI Engineer I BS in mechanical/biomedical/manufacturing engineering Exp: 0-3 years in medical device product development |
The desired individual will possess a broad range of medical device design and development skills and experience, as well as depth of knowledge of process development, process validation, lean manufacturing methodology, and statistical process control. Develop and document manufacturing processes for medical devices (disposable and reusable), catheters, implants, and/or packaging, from concept through market introduction. | 1/6/2020 |
| 12868 | Nordson Elk Grove Village, IL Field Service Technician AS/AA Exp: 0-2 year |
Responsible for performing on-site installation, servicing and repair of complex equipment and systems. Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. | 1/6/2020 |
| 12869 | Nordson Salem, NH Production Associate 1 (Balloons) Third Shift Temp to Hire HS Diploma/GED Exp: 0 years required |
Position consists of manufacturing of medical components in a clean room environment while under general supervision in accordance with specifications and written procedures. This position may include machine operation, manual production using hand tools, visual inspection, physical measurements, and packaging of finished product. This position requires the ability to work with small and delicate components using a high degree of dexterity and accuracy. | 1/6/2020 |
| 12870 | Norwich Pharma Norwich, NY Validation Engineer I BS/BA or work experience Exp: 0-4 years |
The Validation Engineer I - Cleaning conducts validation assessments of equipment, facilities and process systems. Compile and analyze validation data, prepare protocols, reports and make recommendations for changes and/or improvements and maintains appropriate validation documentation and files. | 1/6/2020 |
| 12871 | Norwich Pharma Norwich, NY Technician I Pilot Manufacturing HS Diploma/GED Exp: 1-3 years in manufacturing enviornment |
Primary Responsibilities include: support pilot plant functions. Accurately execute all GMP documentation including batch records, cleaning records, logbooks, etc. Escalates documentation and process errors, events, and deviations immediately to PDTS Manager/Group Leader and PDTS QA. | 1/6/2020 |
| 12872 | Nostrum Laboratories Kansas City, MO Packaging Technician HS Diploma/GED Exp: 1 year in pharma/food/manufacturing |
The Packaging Technician performs routine packaging operations for the production of pharmaceutical products; operates packaging line equipment according to established SOPs and department procedures. Prepares and cleans room, equipment, facility and documents for manufacturing and packaging process | 1/6/2020 |
| 12873 | Notable Foster City, CA Research Associate - High Throughput Screening BS/MS in biological sciences/engineering Exp: 6 months in lab experience |
You will be supporting our numerous projects and be an integral part in scaling up for future upcoming projects. Will be responsible for processing primary samples and preparing them for our automated high-throughput screens. | 1/6/2020 |
| 12874 | Nova Biomedical Waltham, MA Repenishment Associate HS Diploma Exp: 1+ year in distribution/ordering |
Essential Responsibilities are to ensure the accurate movement (stocking, replenishing, consolidating, blocking, fulfilling) of materials and products within the Distribution Department and report any /all batch number or quantity discrepancies related to Distribution materials. Perform cycle counting of assigned materials / products, assist in reconciling variances, identify materials/ products with assigned placards (short-dated, Quality holds, etc.) | 1/6/2020 |
| 12875 | Nova Biomedical Waltham, MA Reagent Packager I - First Shift HS Diploma/GED Exp: 1+ year in related |
The Packager, under general supervision, will follow established procedures in packaging reagent kits. This individual is responsible for working on an assembly line to assemble the various kits within the established quality and time standards. The individual will work with various packaging equipment such as: automated/manual tape machines, manual pallet trucks, conveyors, flow racks and other packaging devices | 1/6/2020 |
| 12876 | Nova Biomedical Waltham, MA Jr Electornic Technician HS Diploma/GED Exp: 1+ year as test technician |
The Jr. Electronic Technician at Nova Biomedical is responsible for operating test and measurement equipment, such as Oscilloscopes and multimeters, to test instruments and assemblies. Essential Responsibilities include: ability to troubleshoot with limited supervision to the component level on low complex boards (thru-hole). Ability to use small hand tools for soldering. Basic knowledge of computers and electronic components. Basic understanding of menu driven computer programs. | 1/6/2020 |
| 12877 | Avecia Pharma Services Irvine, CA Chemist I - QC BS/BA in chemistry or related Exp: 1-2 years in pharma |
Perform routine laboratory analysis of raw material and container closure system samples according to established specifications and procedures using basic analytical chemistry techniques in accordance with Customer, Company and cGMP requirements. | 1/5/2020 |
| 12878 | Nkarta Therapeutics South San Francisco, CA Research Associate MS in molecular/cell biology, immunology Exp: MS: 0-3 years |
The ideal candidate will interact closely with group leaders, scientists and research associate to drive discovery and development of new therapeutics in pre-clinical development. Duties include: Mammalian tissue culture, including isolation and culture of primary human cells from whole blood. Perform studies utilizing cellular immunology to develop and analyze in vitro cell-based assay to support early discovery efforts and pipeline. Perform studies utilizing cellular immunology to develop and analyze in vitro cell-based assay to support early discovery efforts and pipeline. | 1/5/2020 |
| 12879 | Nkarta Therapeutics South San Francisco, CA Research Associate (in vivo) MS in biological sciences Exp: 1 year in pharma/biotech |
Conducts pharmacological evaluation of test agents (cell products or small molecule) in subcutaneous, systemic and orthotopic in vivo oncology models. Assists in sample processing, homogenization, or generation of single cell suspensions for ex vivo flow cytometry analysis or PCR analysis | 1/5/2020 |
| 12880 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior Research Associate MS in biological sciences Exp: 0-3 years in lab |
Execute a broad range of cell based functional and phenotypic assays for characterization of engineered NK and T-cells to accelerate projects in pre-clinical development. Conduct in vitro mechanism of action studies using primary human or mouse immune cells and cell lines to evaluate activity of candidate therapies. | 1/5/2020 |
| 12881 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior Research Associate MS in cell biology or related Exp: 0-3 years in lab |
Generate stable cell lines and master cell banks for both in vitro assays and in vivo pharmacology studies. Oversee and perform daily activities related to the maintenance and scale up of in-house cell lines and primary human immune cells | 1/5/2020 |
| 12882 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior/Process Engineer MS in biological sciences Exp: 1-6 years |
Support process development of phase appropriate cell therapy production processes. Evaluate raw materials and culture systems for use in cell therapy manufacturing processes. Support process optimization efforts to increase process robustness, reduce costs and improve yield | 1/5/2020 |
| 12883 | NeuMoDx Ann Arbor , MI Manufacturing Specialist, Reagent BS/BA in science or chemistry Exp: 1+ year in lab/reagent production |
Manufacturing Specialists are required to have a strong knowledge of manufacturing methods and techniques, process development experience, work flow understanding, ability to understand formulations and follow recipes and testing protocols for any in-process Quality checks | 12/31/2019 |
| 12884 | Neurocrine Bioscience San Diego, CA Associate Scientist, In Vivo BS/BA in biology or related Exp: 1 year or more related experience |
The primary tasks for this position will include transgenic animal colony maintenance and breeding, compound formulation and dosing, behavioral assessments, stereotaxic surgery and tissue collection. This position requires a high level of organization and attention to detail as well as the willingness and ability to work both independently and as part of a team. Previous experience with stereotaxic surgery, AAV administration and mouse colony maintenance preferred. | 12/31/2019 |
| 12885 | Nevro Redwood City, CA Quality Engineer I - Temp BS in technical sciences Exp: 0-2 years in quality/regulatory |
The Quality Engineer I is responsible for Quality Assurance activities related to the life cycle of the product. Trave to and manage manufacturing assembly process at Suppliers. Perform data analysis for root cause investigations | 12/31/2019 |
| 12886 | Nevro Redwood City, CA Firmware Engineer BS in computer engineering or related Exp: 1-2 years, familiarity with C, C++, C# or other |
The Firmware Engineer shall participate in research and product development activities ranging from product concept through transfer to manufacturing. This position will apply knowledge of engineering principles and practices for software development of implantable medical devices and accessories. | 12/31/2019 |
| 12887 | Nevro Redwood City, CA Technial Support Specialist - Temp BS in scientific, technical, or medical field Exp: 1+ year in customer service |
Great Customer Experience is one of the keys to Nevro’s success. The Quality Compliance Specialist is one of the few roles in Nevro that has a direct customer touchpoint to resolve product and therapy questions or issues. This role is critical to ensure that the customer is served as best as we can to ensure that our product and therapy continues to deliver much needed relief to our customers. | 12/31/2019 |
| 12888 | New England Biolabs Bethesda, MD Associate Field Representative - Mid-Atlantic BS in core life sdciences Exp: 1 year in lab preferred |
New England Biolabs (NEB) is seeking a Part-Time Sales Associate to assist the Mid-Atlantic Field Account Manager with prospecting, generating and closing sales leads in the territory. With guidance from the Account Manager, a goal for the Part-Time Sales Associate will be to eventually work independently on assigned accounts. This is a 20 hour a week position. The ideal candidate will live in the Bethesda, MD area. | 12/31/2019 |
| 12889 | New England Biolabs New York, NY Associate Field Representative - Tri-State BS in core life sdciences Exp: 1 year in lab preferred |
New England Biolabs (NEB) is seeking a Part-Time Sales Associate to assist the Tri-State Field Account Manager with prospecting, generating and closing sales leads in the territory. With guidance from the Account Manager, a goal for the Part-Time Sales Associate will be to eventually work independently on assigned accounts. This is a 20 hour a week position. The ideal candidate will live in the Manhattan, NY area. | 12/31/2019 |
| 12890 | New England Peptide Gardner, MA Lab Technician BS/BA in biology or chemistry Exp: 1 year preferred |
Duties include: Operations and maintenance of peptide synthesis instrumentation, liquid chromatography instrumentation, etc. Peptide cleavage data analysis and characterization of peptides using HPLC and Mass Spec. | 12/31/2019 |
| 12891 | New England Peptide Gardner, MA Facility Maintenance AS/AA in industrial/electrical/mechanical engineering Exp: 1-2 years in related |
This role will be responsible for assisting in the completion of the day-to-day activities involving the maintenance of the facility, equipment and machinery and the overall facility appearance. Participate and assist in the maintenance of all company property, including but not limited to, manufacturing equipment, buildings, grounds, HVAC, electrical, plumbing, safety and others as necessary. | 12/31/2019 |
| 12892 | New England Peptide Gardner, MA Lab Assistant HS Diploma or higher Exp: 1 year preferred |
NEP is seeking a highly motivated individual interested in a career in the Biotech/Pharmaceutical industry. Local candidates only. No experience necessary, we will train! Working alongside other Peptide Scientists and Technicians, the Lab Assistant will help support the production process. | 12/31/2019 |
| 12893 | New England Peptide Gardner, MA Lab Technician BS/BA in biology or chemistry Exp: 1 year preferred |
Duties include: Operations and maintenance of peptide synthesis instrumentation, liquid chromatography instrumentation, etc. Peptide cleavage data analysis and characterization of peptides using HPLC and Mass Spec. | 12/31/2019 |
| 12894 | NantKwest La Jolla, CA Research Associate BS Exp: 1 year in lab |
The individual will be responsible for laboratory maintenance, group-support activities to further our NK & T cell initiative from primary tissue sources. This is a great opportunity for a recent college graduate or individual willing to diligently take care of laboratory maintenance and pick up cutting edge scientific skills at the same time to support different projects. Laboratory maintenance that includes ordering, stocking of laboratory and accessory facilities with necessary reagents and supplies. | 12/30/2019 |
| 12895 | NantKwest La Jolla, CA Research Associate BS or MS in biochemistry, biological sciences Exp: 1-3 years as research technician |
Daily tasks associated with the construction and purification of vaccine vectors. Demonstrated proficiency and understanding of concepts of chromatography: HPLC and/or FPLC. Operation and maintenance of laboratory instruments such as centrifuges, incubators, electrophoresis instruments, TFF, imagers, and other measuring instruments and devices. Preparation of laboratory reagents, stocks, cultures, and cell lines | 12/30/2019 |
| 12896 | Natera Austin, TX Production Engineer - Statistics/Data Analysis BS/BA in engineering, bioinformatics, math or related Exp: 0-2 years |
Production Engineer - Statistics performs basic data analysis to manage daily operations for the product and its algorithms. Manage daily operations for the product algorithms. Track ongoing product performance metrics and investigate any variations, in cooperation with lab operations. Investigate data quality concerns using Python/R. Drive informed and timely solutions for unexpected scenarios. Track issues, coordinate new feature releases, and provide data analysis support to laboratory operations. | 12/30/2019 |
| 12897 | Natera San Carlos, CA Quality Assurance Specialist BS/BA in life sciences, engineering or software Exp: 1+ years in biotech |
This is an entry-level position to assist the Quality Department in continuous compliance and improvement. Assist with collecting and trending quality metrics. Assist with assigning IDs for CAPAs, Deviations, SCAR, Complaints, and NCRs and filing completed records. Stays current on applicable regulation and guidance from FDA, ISO13485, CLIA, CAP, etc. Assist with review and approval of qualification records | 12/30/2019 |
| 12898 | Natera San Carlos, CA IQC Associate HS Diploma/GED Exp: 1-2 years in medical device manufacturing |
The IQC Associate conducts incoming material inspections required to assure product safety and compliance to specifications, GMP’s, and ISO requirements. Works with other Quality Inspectors and Laboratory personnel to complete testing, special projects and other projects as required. Ensures compliance with quality systems, policies, procedures and practices and all local, state, federal and safety regulations, policies and procedures. | 12/30/2019 |
| 12899 | Natera Austin, TX QC Equipment Specialist 1 BS/BA in biological sciences Exp: 0-2 years |
The Quality Control Equipment Specialist 1 is responsible to ensure superior performance of all equipment and instrumentation utilized in the Operations laboratory. The QC Equipment Specialist will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications | 12/30/2019 |
| 12900 | Natera Austin, TX Clinical Laboratory Operator I BS/BA in biological sciences Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. Assist in testing of patient samples according to standard operating procedure. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory’s standard operating procedures. Follows GLP (good laboratory practice): maintain clean and organized workspace | 12/30/2019 |
| 12901 | Natera San Carlos, CA Clinical Lab Scientist II BS/BA in med tech/biological sciences, or related Exp: 1-2 years as medical technologist |
Analyzes specimens and maintains equipment in good operating condition. Verify the proper specimen being analyzed and perform tests that need to be completed. Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab | 12/30/2019 |
| 12902 | Natera Austin, TX Clinical Data Operator 1 HS Diploma/GED Exp: 0-1 years |
Clinical Data Operator 1 accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning. Accession samples with high accuracy and efficiency. Accurately enter patient data into the Laboratory Inventory Management System (LIMS). Ensure that the information in LIMS is up-to-date. | 12/30/2019 |
| 12903 | Natus Medical Madison, WI Repair Technician (I or II) AA in relevant field Exp: 0-6 months |
Test and calibrate assemblies to meet quality standards as well as perform electronic calibration and verify fixtures. Trouble shoot assemblies independently with exceptional computer skills. Maintain a strong commitment to high quality work with less than 2% failure rate on repairs. Maintain a 10 business day repair turnaround time on customer owned properties. Maintain minimum stock with refurbished parts to assure same day order fulfillment to assure best in class customer satisfaction | 12/30/2019 |
| 12904 | Natus Medical Boston, MA Field Service Technician AA or equivalent Exp: 6-12 months experience/training |
The Field Service Technician provides industry-best technical support on computer-based medical instrumentation and establishes strong relationships with customers, managers and the national service team. This position will be based remotely and responsible for multi-state service coverage (Region:CT, ME,MA, NH, RI and VT). | 12/30/2019 |
| 12905 | Navitas Life Sciences Rockville, MD Research Specialist - KAI Research BS/BA in biological/health sciences Exp: 0-1 years |
Demonstrate a thorough understanding of the application of basic clinical research methodologies to meet protocol and regulatory requirements. Develop client materials according to project requirements, including but not limited to, project-specific documentation, operating procedures, standards, and work flows. Monitor project changes to ensure documentation and systems/software conforms to new requirements. Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensures appropriate distribution of materials to internal and external research personnel and sites. | 12/30/2019 |
| 12906 | Navitas Life Sciences Rockville, MD Research Assistant - KAI Research BS/BA in biological/health sciences Exp: 0-1 years |
Apply basic clinical research methodologies to meet protocol and regulatory requirements. Assist in the development of client deliverables according to project requirements, including but not limited to, project-specific documentation, operating procedures, and work flows with direction of more experienced staff. Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensure appropriate distribution of materials to internal and external research personnel and sites. | 12/30/2019 |
| 12907 | Nelson Lab Itasca, IL Lab Analyst - Chemistry - M-F, Days HS Diploma/GED to BS Exp: 0-1 years |
The Laboratory Analyst conducts testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. | 12/30/2019 |
| 12908 | Nelson Lab Salt Lake City, UT Lab Analyst HS Diploma/GED to BS Exp: 0-1 years |
The Laboratory Analyst conducts testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. | 12/30/2019 |
| 12909 | Nelson Lab Salt Lake City, UT Development Chemist BS/BA in chemistry or related Exp: 1-3 years |
This position involves decision making in the areas of analytical chemistry, equipment maintenance, data quality, and workflow. Duties include analysis of a wide variety of samples following establish methods or standards, and supporting the development and implementation of laboratory policies and procedures. Experience with instrumentation/equipment and software, such as gas chromatography/mass spectroscopy (GC/MS), high performance liquid chromatography/mass spectroscopy (HPLC/MS), and Inductively coupled plasma/mass spectrometry (ICP/MS). (Ideal candidate needs to have experience with least one of these instruments.) | 12/30/2019 |
| 12910 | Neocis Miami, FL Control Software Engineer BS in computer science/electrical engineering Exp: 0-2 years |
Neocis is looking for a robot control software engineer to contribute significantly to the core design. You will be responsible for software design and development of a real-time robot controller, verification and validation testing for safety and reliability and support and contribute to intellectual property development. You will work with cross-functional teams including software and electrical engineers and marketing as well as clinicians and clinical staff. | 12/30/2019 |
| 12911 | Nephron Pharma West Columbia, SC Quality Assurance OnlineEvening 12 hour Shift ONLY HS Diploma/GED Exp: 1-2 years in QA/Production |
Performs Weight Check and Quality Attributes Inspection of the product through the filling and packaging process in compliance with company policies / procedures, FDA and cGMP regulations. Ensures the accuracy and completeness of batch records. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. | 12/30/2019 |
| 12912 | Nephron Pharma West Columbia, SC Microbiology Analyst I BS in biological/life sciences Exp: 1 year in pharma preferred |
Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Demonstrate high proficiency level on tests performed. Apply quality scientific techniques in the microbiological analysis of raw materials; in-process & finished product samples to include: sterility, bioburden, identification, environmental monitoring, growth promotion, microbial recovery and media fill tests following approved procedures. | 12/30/2019 |
| 12913 | Vicarious Surgical Charlestown, MA Artificial Intelligence Engineer MS in computer science Exp: 1-3 years |
Joining the Research & Development team as an Artificial Intelligence engineer, you will lay the groundwork for a brand new team at Vicarious Surgical giving intelligence to the next generation of surgical robotics. We are looking for dynamic, collaborative individuals with a passion for AI who thrive in a fast-paced, creative, and strategic environment. You will enjoy working with a highly talented and diverse team of engineers to develop Artificial Intelligence, Perception, Computer Vision, and Robotic Controls features for our robots. This job entails: Research and develop technologies for conventional AI, Computer Vision, Machine Learning, multi-sensory perception, sensor fusion, scene understanding etc. for robotics applications. etc. | 12/17/2019 |
| 12914 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Tuesday - Saturday, 1:00 AM to 9:30 AM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. etc. | 12/17/2019 |
| 12915 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Tuesday - Saturday, 8:00 AM to 4:30 PM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. etc. | 12/17/2019 |
| 12916 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Monday - Friday, 8:00 AM to 4:30 PM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. etc. | 12/17/2019 |
| 12917 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Tuesday - Saturday, 12:00 PM to 8:30 PM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. etc. | 12/17/2019 |
| 12918 | Viracor Lee's Summit, MO IT Business Analyst I AS/BS in laboratory science Exp: 1-2 years |
This is a Full Time position. Schedule is Monday - Friday, 8:00AM – 5:00PM, with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The IT Business Analyst supports the organization by assessing the impact of requested changes, capturing and documenting requirements, and ensuring that those requirements are delivered by IT. In addition, the Business Analyst is responsible for the documentation and execution of test plans for the delivered functionality while supporting the business through the implementation process. Business Analysis is part of the Software Development Life Cycle (SDLC) and the Business Analyst will be involved from initial concept through final implementation, including requirements gathering, design, testing and implementation. Employee Responsibilities: Consult with different areas of the organization to identify and document the requirements for new systems and enhancements to existing systems. Document business functions and processes using a best practice standard developed by the Business Analysis team. etc. | 12/17/2019 |
| 12919 | Viracor Lee's Summit, MO Research Scientist I BS/BA in a laboratory science Exp: 0-3 years |
This is a Full Time position. Schedule is Monday – Friday, 1:00pm- 9:30pm with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Research Scientist is primarily responsible for conducting research, development, validation and execution of assays to meet the development requirements within corporate/client timelines and cost objectives. Employee Responsibilities: Learn new techniques and instrumentation. Implement research plans, designs and testing protocols. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Keep accurate documentation of all research project steps according to Viracor Eurofins regulatory guidelines. etc. | 12/17/2019 |
| 12920 | Viracor Lee's Summit, MO Research Scientist I BS/BA in a laboratory science Exp: 0-3 years |
This is a Full Time position. Schedule is Monday – Friday, 8:30pm- 5:00pm with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Research Scientist is primarily responsible for conducting research, development, validation and execution of assays to meet the development requirements within corporate/client timelines and cost objectives. Employee Responsibilities: Learn new techniques and instrumentation. Implement research plans, designs and testing protocols. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Keep accurate documentation of all research project steps according to Viracor Eurofins regulatory guidelines. etc. | 12/17/2019 |
| 12921 | Visterra Waltham, MA Research Associate BS in biochemistry or related Exp: 1 year |
Visterra, Inc., is looking to hire a highly motivated Research Associate with research experience in biochemistry, protein sciences and/or molecular biology applied in the context of antibody-based therapeutic drug discovery. This individual will play a key technical role in advancing Visterra’s early research programs in autoimmunity, immunology and other related areas of therapeutic interest through the design and implementation of library-based screening methods, recombinant protein production, protein engineering, and biochemical, biophysical, and biological characterization of early and late stage leads to support the discovery andvalidation of therapeutic antibody candidates. etc. | 12/17/2019 |
| 12922 | Voyager Therapeutics Cambridge, MA Clinical Trial Associate (Contract) BS in a life science Exp: 0-2 years |
The Clinical Trial Associate (CTA) will support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. The CTA will also assist the CTM for assigned studies in the operational and logistical aspects of clinical trials according to ICH-GCP and Voyager standard operating procedures. This position reports in directly to the Associate Director of Clinical Operations. Responsibilities: Support project meeting logistics such as: calendar management, room & equipment set up, attendance tracking, agenda preparation, drafting of meeting minutes, and collation of materials. Set up, maintain and periodically audit Trial Master Files and ensure all relevant study documents are filed and archived based on the appropriate guidelines/processes. Execute assigned study tasks, awareness of priorities and timelines, assist in tracking study metrics, maintenance and distribution of trackers, support preparation of study newsletters, communicate with and oversee CRO for assigned start-up activities. etc. | 12/17/2019 |
| 12923 | Voyager Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Molecular Biology BA/BS Exp: 1-3 years |
Voyager Therapeutics seeks a highly motivated and experienced molecular biologist to contribute to its research team at its facility in Cambridge, Massachusetts. The candidate will be involved in novel AAV capsid discovery, screening AAV variant libraries in small and large animals and engineering capsids for desired properties. This is an ideal position for an individual with extensive hands-on cellular and molecular expertise, who has a can-do attitude and strong work ethic, and thrives in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment. Requirements: Molecular cloning and prepare rAAV constructs or AAV capsid libraries. Perform plasmid purification by miniprep and maxiprep. Maintain and culture mammalian cell lines, perform transient transfection for gene expression or AAV vector production at a small or medium scale. etc. | 12/17/2019 |
| 12924 | WAVE Life Sciences Cambridge, MA Research Associate – Biology BS/MS in biology or related Exp: 0-3 years |
WAVE Life Sciences USA seeks a highly motivated biologist to join its research team in Boston, Massachusetts. This is an ideal position for an individual who is interested in learning cutting edge technologies and who thrives in a team-oriented, fast-paced, and crossdisciplinary biotech environment. The candidate will be responsible for designing, executing and analyzing experiments as a member of teams focused on advancing therapeutic programs and discovery research platforms. This candidate will contribute to all levels of in vitro and in vivo discovery research to support development of optimized nucleic acid therapies in multiple disease areas. Prior experience in animal handling and tissue processing are preferred, but not required. Position Responsibilities: Experience in cell and molecular biology, including primary cell culture, transfections, mRNA quantitation by qPCR, and protein quantification by ELISA or western blot. etc. | 12/17/2019 |
| 12925 | WCCT Global Cypress, CA Laboratory Accessioner HS diploma or equivalent Exp: 3-6 months |
The Laboratory Accessioner is responsible for entering all patient information, demographics, and ordered tests in the laboratory information system. The Accessioner will QC daily data entry and work under the direct supervision of the Research Laboratory Supervisor. Daily tasks include organizing requisition forms, data entry, filling out send out requisitions for outside testing, cleaning up work area, and performing waived testing. Essential Job Functions: Enter all pertinent information from the requisition into the computer correctly. Enters "special handling" and/or frozen requisitions. When handling frozen samples, will set up work areas by retrieving dry ice, ice chests, racks, and stickers. Accessioners will also be responsible for signing for the integrity of frozen specimens, received from the couriers. At the end of each night, the accessioners will deliver the specimens to the appropriate departments. Take complete inventory of contents of envelope. etc. | 12/17/2019 |
| 12926 | WCCT Global Cypress, CA Laboratory Assistant HS diploma or equivalent Exp: 3-6 months |
The Laboratory Assistant is responsible for conducting the biological sampling activities related to each clinical trial. This position assists with the preparation, collection, documentation, processing, inventory and shipment of biological specimens for each study and reports to the Laboratory Supervisor. ESSENTIAL JOB FUNCTIONS: Conducts all operational activities within the laboratory related to the preparation of sample collection containers, processing biological specimens, performing testing, documenting procedures, and preparing specimen shipments. Ensures that all lab procedures are done correctly with minimal error. Follows the policies and procedures for laboratory facilities and equipment maintenance. etc. | 12/17/2019 |
| 12927 | WCCT Global Cypress, CA Phlebotomist/Medical Assistant - On Call HS diploma or equivalent Exp: 3-6 months |
The On Call Research Assistant is an entry level position assisting in a variety of duties involved in the collection, compilation, and documentation of clinical research data in various departments as assigned. All data collected is quality control reviewed and is compliant with study and non-study regulations including, but not limited to the study protocol, HIPAA, OSHA, GCP, GDP, CFR, ICH Guidelines and site SOPs and Work Instructions. ESSENTIAL JOB FUNCTIONS: Follow all study and non-study regulations including, but not limited to: Patient/Volunteer Privacy (HIPAA), OSHA, Good Clinical Practice (GCP), Good Documentation Practice (GDP), Standard Operating Procedures (SOP), and department specific Work Instructions (WI). Follow proper safety and emergency policies and procedures as set forth by WCCTG. etc. | 12/17/2019 |
| 12928 | Westat Rockville, MD Research Assistant BA/BS in social sciences or education Exp: 1 year |
Westat has an immediate opening for a research assistant who will work with a project team to train and support staff in state education agencies to implement a national assessment of students and to develop data analyses and reports. Provide analytical and operational support to the project and to staff in state education agencies; Develop and manage training materials; conduct web-based and in-person trainings; Provide secondary support to project Support Desk and project intranet website on an as-needed basis; Develop and maintain project schedule of web-based trainings; Review and manage data for quality control purposes and project evaluation, maintain and enhance databases of project information; Monitor the productivity and quality of the data collection effort; Work with IT and project staff on system requirements. | 12/17/2019 |
| 12929 | Westat Rockville, MD Research Assistant MS/MA in a quantitative social science Exp: Not necessary for MS/MA candidates |
Westat is seeking a research assistant to work on survey research projects, assisting expert data managers in defining and processing survey data and metadata from collection through delivery to Westat’s clients. Data review and documentation writing are both part of the role. Write technical specifications for programming survey instruments and analytic variables. Define data dictionaries for complex files, test survey instruments to ensure accurate data capture, and review collected data at the detailed level. Create data descriptions and harmonize data from multiple sources; the data are collected in a variety of technologies and formats with a wide breadth of subject areas. etc. | 12/17/2019 |
| 12930 | Westat Rockville, MD Research Assistant BS/BA Exp: 1 year |
We have an immediate opening for a research assistant with experience in data collection procedures and materials along with a background in quantitative research and data analysis. The successful candidate will work closely with a multidisciplinary research team working on an innovative longitudinal health and aging study and a caregiving study. Job Responsibilities: Develop specifications for computer-assisted survey data collection instruments. Draft instrument testing scripts and related materials. Working with project and IT staff on technical specifications for survey management systems. Assist in developing data collection procedures, respondent materials, and field memos. etc. | 12/17/2019 |
| 12931 | Wolfe Laboratories Woburn, MA Research Associate BS/MS in chemistry, biochemistry, or related Exp: Recent graduates |
We are seeking a talented and passionate scientist who is eager to be part of our success, and who embraces our core values: Integrity, Excellence, and Teamwork. This role requires a highly driven and proactive scientist with a passion for drug development, the curiosity and flexibility to work on diverse projects, and the tenacity to tackle complex questions by developing/applying new methods to solve previously intractable problems in drug development in a dynamic, fast-paced, team-oriented and collaborative environment. etc. | 12/17/2019 |
| 12932 | Worldwide Clinical Trials Austin , TX Bioanalysis Support BS Exp: 0-2 years |
The Scientific Associate, Bioanalysis Support works under the guidance of the Senior Manager, Leader of Bioanalysis and is responsible for providing support and performing analyses ranging from routine to complex using accurate and efficient analytical techniques. Understand and apply GLP guidelines in all aspects of work. Perform chemical assays ranging from routine to complex with consistent accuracy and precision. Accurately prepare stocks, reagents, standards and quality controls as needed. Work with a variety of scientists/technicians. Perform basic mathematical calculations. Document promptly and clearly all procedural processes. etc. | 12/17/2019 |
| 12933 | WuXi AppTec San Diego, CA Research Associate I AS/BS in biology or related Exp: 0-1 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate I to join the team. Responsibilities: Assist with in vivo pharmacology experiments for preclinical contract research. Perform in vivo studies to evaluate anti-cancer efficacy of test agents in tumor mouse models with supervision. Monitor mouse groups enrolled in drug efficacy, mechanism of action, PKPD and proof-of-concept studies. Perform drug dosing by various routes of administration. Perform in-life blood sampling through various routes. Perform necropsy and tumor/organ sampling and processing. Monitor in-life study measurements: tumor volume, body weight, tracking overall health condition and survival of mice. etc. | 12/17/2019 |
| 12934 | WuXi AppTec Cranbury, NJ Associate Scientist I BS in animal science, biology, or related Exp: 0-3 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC standards. Operates lab equipment including oxidizers, centrifuges, LS counters, and cage/tunnel washers. Essential Job Functions: Under regular close supervision, performs routine in vivo experimental functions in rodents, which may include: in life observations, dose administrations, sample collections, sample analysis, necropsy, and euthanasia procedures. Trains on various techniques to become proficient in in vivo. Performs husbandry tasks including observations, cage change outs, daily cleaning, and operating the cage washer. Assists with routine vivarium facility environmental monitoring (RODAC, pest control, lighting checks, etc.). etc. | 12/17/2019 |
| 12935 | WuXi AppTec King of Prussia, PA Scientist Downstream Process Development BS/MS Exp: 0-5 years |
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine Downstream cell culture processes. Responsibilities: Work independently on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. Design and execute lab-scale experiment in supporting downstream process development, verification, characterization. Perform purification experiments in BSL-2 labs and document experiments in lab notebooks. Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside clients/vendors/suppliers. | 12/17/2019 |
| 12936 | WuXi AppTec King of Prussia, PA Scientist Upstream Process Development BS/MS Exp: 1-2 years |
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. Responsibilities: Work on defined biopharmaceutical projects for development and/or characterization of vaccine upstream manufacturing cell culture processes. Perform bench scale and pilot scale bioreactor operations in supporting upstream process development, verification, characterization, and tech transfer. Perform data analysis and interpretation, and develop strategies for optimization and troubleshooting. Support technical transfer of processes into the non-GMP pilot plant or GMP production facility. etc. | 12/17/2019 |
| 12937 | WuXi AppTec Austin , TX Clinical Project Associate HS diploma/AA/AS Exp: 1 year |
The Clinical Project Associate I provides administrative support to clinical research projects by assisting project teams in the completion of assigned project activities. This is an in-office position with that does not require travel. Provides operational support for Clinical Operations. Under direct supervision prepares, reviews and distributes the regulatory documentation according to Essential Regulatory Document Guidelines and Trial Master File (TMF) Plan. Under direct supervision prepares the investigator regulatory binders and other study start-up materials, following established procedures. Under direct supervision designated Clinical Trial Management System (CTMS) to track and process clinical trial information, (e.g., site lists/personnel, regulatory documents, Institutional Review Board re-approvals) in order to provide analysis of information to PM. Prepares and provides status reports to customers with oversight from assigned PM. Under direct supervision assures the maintenance of the TMF. etc. | 12/17/2019 |
| 12938 | WuXi AppTec Philadelphia, PA Research Associate, Analytical Development - Virology BS in a biological science Exp: 1+ year(s) |
Performs research & development activities and assay validations as required under direct supervision. Drafts test methods and clearly documents all experiments according to SOPs and cGMP guidelines. Performs laboratory maintenance duties. Works closely with Testing Operations during assay transfer and validation activities. Responsibilities: Executes R&D studies planned by supervisor or technical lead. Works under close supervision from supervisor or senior personnel. Executes QP and VPs, and other GMP methods under supervision by supervisor or technical lead. Drafts test methods/RPs/SOPs under guidance of supervisor or technical lead. etc. | 12/17/2019 |
| 12939 | Miltenyi Biotec Auburn, CA Accounting Associate AS/AA Exp: 1-3 years in business/accounting |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. You will use your collaborative nature to effectively coordinate intercompany communications and transactions with various departments, with management, and the parent company to enable the continuous success of Miltenyi Biotec as a whole. | 12/15/2019 |
| 12940 | Miltenyi Biotec Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years in clinical processing/cell culture |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. Overall, your keen ability to carry out key cell processing and manufacturing procedures will champion the continued development of Miltenyi Biotec products and growing success. | 12/15/2019 |
| 12941 | Miltenyi Biotec Sunnyvale, CA Process Development Associate BS/BA in life sciences Exp: 0-2 years |
As a member of Miltenyi Biotec’s Process Development team, you will have the exciting opportunity to support the development of new processes that will generate cellular therapeutic products. You will apply your GLP/GMP experience to perform and maintain cell cultures using aseptic techniques. Ideally, you will be able to order materials and maintain inventory with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical cell and gene therapy products. In addition to your primary responsibilities, you will document activities for reproducibility, clean and maintain laboratory equipment and support team members as needed. Your superb organizational and documentation skills will be instrumental in the tracking and communication of data and will ensure efficient progress towards achieving team objectives. Overall, your attention to detail and keen ability to reliably produce cell cultures in a cross-functional team will champion the continued development of Miltenyi Biotec’s new products and growing success. | 12/15/2019 |
| 12942 | Miltenyi Biotec Gaithersburg, MD Research and Development Scientist, RCL/HIV MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to perform duties within the area of development of new tests, including the development of a standard RCL test and in a second instance of an automatized RCL test. This includes the set-up of a standard test based on the use of C8166 cells, the characterization of the C8166 cells with respect to susceptibility and propagation of HIV over many cell passages, etc. A very issue related to this development is that the test has to comply with FDA requirements with at the end the transfer of the test to the QC department for routine use. Furthermore, you will be involved in the automatization of this specific test and eventually of other tests in the future. In this context, you will be directly involved in the conceptualization of such a test, responsible for designing specific experiments and analyzing the data using appropriate statistical methods. The particular duties of this position will allow you to work as part of a collaborative team environment | 12/15/2019 |
| 12943 | Miltenyi Biotec Gaithersburg, MD PD Associate I BS/BA Exp: 0-2 years |
As a member of the Lentigen Technology Process Development team, you will have the exciting opportunity to support the development and tech transfer of processes to manufacture purified Lentiviral vectors used for pre-clinical and clinical products. You will apply your knowledge and prior laboratory experience to support the pre-clinical and clinical manufacturing of Lentiviral vector products. Familiarity with cell culture and/or purification technologies and analytical methods will enable you to assist in the development and tech transfer of processes compliant with GMP manufacturing requirements. | 12/15/2019 |
| 12944 | Miltenyi Biotec Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years in clinical processing/cell culture |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. | 12/15/2019 |
| 12945 | Miltenyi Biotec San Diego, CA Executive Assistant AS/AA in business or related Exp: 0-2 years |
As a key member of the Miltenyi Biotec team, you will have the opportunity to provide administrative support to the President as well as other department heads in assigned activities. The unique duties of this position will allow you to oversee schedules, track activities, and serve as key contact between executives and internal/external clients. Additionally, you will assist in preparing agendas and presentation materials for associated events, meetings, and seminars. Overall, your particular skillset and efforts will drive Miltenyi Biotec’s continuing business success. | 12/15/2019 |
| 12946 | Miltenyi Biotec Gaithersburg, MD R&D Scientist, Purification & Characterization MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to develop methods for the separation of different particle types and their characterization. Also, you will develop, evaluate and implement novel analytical methods for the fine characterization of viral vectors and exosomes, in view of the distinction of viral vectors from exosomes. You will design specific experiments to test LV function, perform statistical analysis of results, and communicate results internally, for use in publications, and in scientific meetings. Your responsibility will also include the development of chromatography-based separation steps in-view of the optimization of an existing purification protocol and their standard characterization. | 12/15/2019 |
| 12947 | Mirus Madison , WI Shipping and Product Finishing Assistant HS Diploma/GED Exp: 1-2 years |
This position is required to provide department coverage 11am-3pm Monday-Friday. The position is offered at 32-40 hours per week. Prepare and execute domestic and international shipping of Mirus products using FedEx, UPS, DHL and freight forwarders. Receipt of incoming deliveries (e.g. supply orders, freight and parcel deliveries) | 12/15/2019 |
| 12948 | Mission Pharma Boerne, TX Particle Technician HS Diploma/GED Exp: 1 year related experience |
Produces bulk pharmaceuticals, operates machinery and equipment, handles raw materials with and without handling equipment, completes documentation, and cleans and sanitizes equipment and rooms per SOP’s. Performs duties such as weighing, labeling, storing, moving, raw materials. Operates a mixer, forklift, powered pallet jacks, scales, dust collectors, hand tools, Fitzmill and sifter, NOL-TEC system and moisture removal controller. Weighs out and sample finished product. Processes the finished product for transport. Performs mixing duties such as introducing materials into the mixer, watching for overflow, dumping materials, scraping the inside of mixers and transfer s materials to drying racks and/or bins. | 12/15/2019 |
| 12949 | Qiagen Frederick, MD QC Associate Scientist II MS in biological sciences Exp: 0-2 years |
Perform routine testing on manufactured products including incoming raw materials, in-process products, and finished goods. Testing covers reagents of multiple product groups with a focus on NGS-related panels, chemistry, and indices using NGS platforms and various PCR platforms. Support tech transfer and QC workflow implementation during new product transfer and launch. These include performing validation tests, help to writing of instruction and protocol/SOP. Support continuous quality improvement by conducting tests for root cause analysis, or for revised QC process validation, or for new QC instrument verification and validation. | 12/15/2019 |
| 12950 | Qiagen Beverly, MA QA Associate BS/BA Exp: 1-3 years in QA |
The QA Associate role assists with all QA compliance activities; including reviews of CAPAs, deviations, NCMRs, customer complaints and recalls. Position responsibilities also include participation at internal and external regulatory audits, document reviews and support of companywide QA initiatives. | 12/15/2019 |
| 12951 | Qiagen Germantown, MD Technical Associate - Kit Assembly Operations HS Diploma/GED Exp: 1-3 years |
The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. Responsible for Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. Assist in the setup and preparation of required production related materials. | 12/15/2019 |
| 12952 | Qiagen Germantown, MD Technical Associate - Automated Assembly Operations HS Diploma/GED Exp: 1-3 years |
The 2nd shift Technical Associate in Production and Assembly comprehends and performs assigned automated and manual production tasks according to established standard operating procedures. Responsible for Automated and/or Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of automated assembly equipment, as well as other production related equipment within the assembly area. | 12/15/2019 |
| 12953 | Qiagen Mobile, AL Field Service Specialist (Mobile, AL area) BS/BA in sciences, med technology, or engineering Exp: 0-3 years |
On site Field support of QIAGEN, Peak Service and Excalibur supported instrumentation. Position based in Mobile, AL area. Install, maintain, troubleshoot, repair, and support instruments on all levels (Hardware and Software). Maintain and develop positive relationships with customers and references. Assist in meeting/exceeding sales targets and related KPI's in relation to maintaining high customer satisfaction. Ensure all paperwork is completed accurately, in a timely fashion and in lines with any regulatory requirements. Utilize relevant databases to input and provide information to the organization. | 12/15/2019 |
| 12954 | Moderna Cambridge, MA Candidate Experience Associate HS Diploma/GED Exp: 1 year in HR environment |
This role is the steward of Moderna’s candidate experience at every step of our recruitment process. The ideal hire for this role is curious about people, is completely ‘customer focused’ and has a desire to grow their career in Talent Acquisition or Human Resources. Partner with our Talent Acquisition Team and Hiring Leaders to provide a streamlined and efficient interview scheduling process. Create and communicate interview schedules, travel and hotel details to talent and third party executive search partners. Help define and reinforce a consistent interview scheduling process at Moderna that results in a superior candidate and hiring manager experience. This includes pushing back, where needed, and educating others on SLA’s (service level agreements). | 12/15/2019 |
| 12955 | Moderna Cambridge, MA (Contract) Sr. / Research Associate, Cell-based Assay Development MS in biological sciences Exp: 0-2 years |
The individual will participate in the development and performance of cellular and biochemical assays to support advancement of Moderna’s mRNA clinical development candidates. Standard mammalian cell culture support including maintaining and plating of cell lines. Development of in vitro assays (e.g. immunoassay, ELISA, PCR, Western blot, luminescence, bDNA, functional activity) using cultured mammalian cells to support product development. Optimize assay performance (precision, accuracy, robustness) and implement high throughput sample testing to support product development The individual will participate in the development and performance of cellular and biochemical assays to support advancement of Moderna’s mRNA clinical development candidates. Standard mammalian cell culture support including maintaining and plating of cell lines. Development of in vitro assays (e.g. immunoassay, ELISA, PCR, Western blot, luminescence, bDNA, functional activity) using cultured mammalian cells to support product development. Optimize assay performance (precision, accuracy, robustness) and implement high throughput sample testing to support product development The individual will participate in the development and performance of cellular and biochemical assays to support advancement of Moderna’s mRNA clinical development candidates. Standard mammalian cell culture support including maintaining and plating of cell lines. Development of in vitro assays (e.g. immunoassay, ELISA, PCR, Western blot, luminescence, bDNA, functional activity) using cultured mammalian cells to support product development. Optimize assay performance (precision, accuracy, robustness) and implement high throughput sample testing to support product development | 12/15/2019 |
| 12956 | Moderna Cambridge, MA (Contract) Research Associate, Analytical Operations BS or MS Exp: BS: 1-3 years, MS: 0-2 years |
The primary responsibilities of this role will be to support development and performance of analytical methods for messenger RNA therapeutic drug substance and drug products. The incumbent will be expected to undertake laboratory work to support testing and data collation. Additional responsibilities include developing high throughput methods using liquid handling and end-to-end sample tracking for drug substance/product components and impurities. This position will support cross-functional teams in Research and Development, Production and Quality. Additionally it is expected that the role will require the individual to generate technology transfer documents and enable the physical transfer of methods to receiving groups as part of a broader functional responsibility. The anticipated time frame for this assignment is six months. | 12/15/2019 |
| 12957 | Moderna Cambridge, MA (Contract) Document Associate BS in related Exp: 1-2 years in regulatory operations |
This role is an exciting opportunity to be an integral part of the talent engine fueling a high growth organization that is radically changing the biotech industry. Reporting to the Senior Director, Regulatory Operations, the Document Associate, Regulatory Operations will be responsible for assisting with document formatting, publishing, quality control, and interactions with third party vendor(s) to ensure compilation of high-quality electronic submissions. | 12/15/2019 |
| 12958 | Danaher Fremont, CA Customer Success Representative HS Diploma/GED Exp: 1-3 years in customer service |
In this role you will have an impact on the customer experience, helping to create and sustain customer loyalty through enablement of their success. A successful candidate will have a positive attitude with the ability to readily adapt to change and solve problems. Additionally, the candidate should be able to demonstrate empathy for both internal and external customers, and will be expected to work closely with sales, product support, repair teams, and customer support to create value and enable an exceptional customer experience. | 12/15/2019 |
| 12959 | Molecular Templates Austin, TX Research Associate BS/BA in life sciences Exp: 1 year in lab setting |
This position will perform functions related to production of pre-clinical drug product and early-stage process development for protein sciences, including routine protein purification, equipment maintenance checks and calibration, data management, and assist in review and development methods and procedures to control or modify the process. This position will also aid in identifying continuous process improvement areas. This will require excellent technical, analytical and organizational skills, along with adherence to written and verbal instructions and accurate and timely completion of manufacturing batch records. | 12/15/2019 |
| 12960 | Molecular Templates Austin, TX downstream process development AS/AA in biotechnology preferred Exp: 1-2 years previous experience preferred |
This position will be responsible for working with fellow team members to develop robust, efficient and scalable methods for protein purification/manufacture. This position will perform functions related to downstream process development of recombinant biologics, including experimentation involving protein purification, cell lysis, clarification, chromatography, ultrafiltration, diafiltration and filling. Additional activities will include solution preparation, equipment maintenance and calibration, data management, report authoring, and review of manufacturing processes. | 12/15/2019 |
| 12961 | Molecular Templates Austin, TX Associate Scientist BS/BA in life sciences Exp: 1 year in lab setting |
The Associate Scientist will be responsible for working with fellow team members to develop robust, efficient and scalable methods for protein purification/manufacture. This position will perform functions related to downstream process development of recombinant biologics, including experimentation involving protein purification, cell lysis, clarification, chromatography, ultrafiltration, diafiltration and filling. Additional activities will include solution preparation, equipment maintenance and calibration, data management, report authoring, and review of manufacturing processes. | 12/15/2019 |
| 12962 | Molecular Templates Austin, TX Manufacturing Associate AS/AA in life sciences, engineering or related Exp: 1 year or more in GMP manufacturing |
This position will perform functions related to production and GMP manufacturing operations, including execution of protein fermentation steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. | 12/15/2019 |
| 12963 | Molecular Templates Austin, TX Manufacturing Associate AS/AA in life sciences, engineering or related Exp: 1 year or more in GMP manufacturing |
This position will perform functions related to production and GMP manufacturing operations, including execution of protein purification steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. | 12/15/2019 |
| 12964 | Mylan Sugar Land, TX Quality Assurance Specialist MS in pharma/med devices Exp: 0-2 years |
Perform quality assurance documentation record review and batch disposition. Determines the disposition (i.e. release or rejection statuses) for packaging components (container/closures), raw materials, bulk products and finished packaged products. Assists in compiling data for Annual Product Reviews. Assists in QA product complaint activities which include: Daily electronic reviews - Logging – Investigating- Trending. | 12/15/2019 |
| 12965 | Mylan Greensboro, NC Quality Technician, Inspections- 2nd Shift BS/BA Exp: 0-2 years |
Coordinate release documents, perform product releases in SAP, and perform product inspections. Write specifications and SOP’s, perform warehouse investigations, review rejections, place products on quality hold, process sample requests, returned goods and donations, ship studies, and review temperature data. Process sample requests as requested. Process and/or review returned goods and assign disposition. Process shipping studies when received. | 12/15/2019 |
| 12966 | Myriad Genetics Salt Lake City, UT Laboratory Technician BS or MS in sciences Exp: 0-2 years |
The Laboratory Technician is responsible for specimen processing, testing and monitoring test performance. The technician must demonstrate competency, as defined in the department’s training program, prior to performing independent testing. This position will work with department management and quality team members to ensure that laboratory activities are defined, documented and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation and continuous improvement projects. | 12/15/2019 |
| 12967 | Myriad Genetics South San Francisco, CA Intake Associate BS/BA Exp: 0-2 years |
At Myriad Women's Health, the Intake team is responsible for the timely and accurate data entry and management of patient orders. You will be a significant contributor to our high-throughput workflow and an integral part of our busy CLIA lab. Input and manage patient data from a variety of sources, and ensure that orders are fully processed at the highest level of accuracy. Identify issues and trends and collaborate with your team and leadership to develop best practices to ensure we are providing the best service and experience to all customers | 12/15/2019 |
| 12968 | Myriad Genetics Salt Lake City, UT Laboratory Technician III MS in clinical lab science, chemical, physical or biological science Exp: 6 months |
The Laboratory Technician III is responsible for specimen processing, testing and monitoring test performance. The technician must demonstrate competency, as defined in the department’s training program, prior to performing independent testing. This position will work with department management and quality team members to ensure that laboratory activities are defined, documented and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation and continuous improvement projects. | 12/15/2019 |
| 12969 | Myriad Genetics Salt Lake City, UT Clinical Laboratory Assistant HS Diploma/GED Exp: 1-3 months |
Myriad Autoimmune is seeking a Clinical Laboratory Assistant to assist in the preparation of sample aliquots; retrieving samples for testing as directed by work schedule; performing inventories and orders for laboratory and office supplies; performing clerical duties that do not involve interpretation or judgment; receiving and accessioning samples into the CLIMS; and assisting CLS' with various lab duties (temperature monitoring, CLIMS sample batching, preparation of buffers), reporting issues to management. | 12/15/2019 |
| 12970 | Myriad Genetics Salt Lake City, UT Laboratory Technician BS in chemical, physical, biological or clinical laboratory/medical technology science Exp: 0-2 years |
The Laboratory Technician in the LegacyX Lab is responsible for preparing high-performance liquid handling robots for specimen processing. The technician must maintain patient sample integrity through demonstrating competency and repeatability in performing specimen processing as defined by the department’s standard operating procedures. This is a production environment, not a research environment. Pay starts around $18/hour depending on experience. | 12/15/2019 |
| 12971 | Myriad Genetics Austin, TX RBM Laboratory Technician - Testing BS/BA in engineering/sciences Exp: 0-3 years |
The goal of the Lab Technician I is to ensure that process’s required for a production run as it pertains to samples and reagents are done in an organized and expedient manner. The Technician is accountable for following company procedures and working to the best of their ability to ensure quality in all aspects of the job. | 12/15/2019 |
| 12972 | NAMSA Irvine, CA Microbiology Technologist BS/BA Exp: 0 years |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. | 12/15/2019 |
| 12973 | NAMSA Northwood, CA Lab Technologist - In Vivo BS in sciences Exp: 0-3 years |
May prepare all testing/test article and animals according to written instructions and protocols. May execute routine testing per NAMSA SOPs, with appropriate data analysis. May communicate test schedule updates to NAMSA management as needed. May prepare and maintain reagents and/or test articles as required for testing.May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. | 12/15/2019 |
| 12974 | NAMSA Irvine, CA Microbiology Technologist BS/BA Exp: 0 years |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitor. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. | 12/15/2019 |
| 12975 | Nanostring Seattle, WA Manufacturing Research Associate I/II BS/BA in sciences Exp: 0-2 years in lab |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 12/15/2019 |
| 12976 | Nanostring Bothell, WA Manufacturing Research Associate I BS/BA in sciences Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 12/15/2019 |
| 12977 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in biology/chemistry Exp: 0-2 years in biotech/pharma |
The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. | 12/15/2019 |
| 12978 | Upsher-Smith Maple Grove, MN Network Systems Analyst I BS in computer science or related Exp: 0-2 years |
The Network Systems Analyst will be primarily responsible for managing and configuring security information and event monitoring (SIEM) tool. Research security enhancements and identifies solutions to enhance IT security. Evaluates and recommends security products, services, and/or procedures to enhance productivity and effectiveness. Provides technical support of IT infrastructure at all Upsher-Smith locations. Support will include assisting with installation, configuration, recovery, administration and security of infrastructure components. Incumbent will work on implementation projects as well as have responsibility for daily monitoring and support activities. etc. | 12/10/2019 |
| 12979 | Upsher-Smith Maple Grove, MN Corporate Sales Representative BS/BA in business, science, communication or related Exp: 1-3 years |
The Corporate Sales Representative is responsible for the development and management of a designated territory with the goal of maximizing sales while improving patient lives. Patients are central to all USL strategies, and the CSR will be responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other healthcare practitioners and members of the health care community. The CSR may work in a team with a Corporate Sales Specialist (CSS), Regional Trainer, Managed Care - Regional and National Account Manager to increase sales, market share and profitability of USL products. Time allocation of 75% inside sales and 25% field sales is expected; however, this may vary as business needs arise. | 12/10/2019 |
| 12980 | United States Biological Salem, MA Information Technology and Marketing Associate BS/BA in computer science Exp: 1+ year(s) |
United States Biological is a local, growing manufacturing company seeking enthusiastic individuals to be part of our team. We specialize in thousands of antibodies, ultra pure molecular biology reagents, cell culture media and enzymes. Troubleshoot and provide hands-on support to all personnel. Work with company president on all areas of website, graphics and IT. Set up and format new workstations as needed. Design and create newsletters. Maintain systems, databases and website, as needed. | 12/10/2019 |
| 12981 | Veeva Toronto, ON Associate Software Engineer BS in computer science, engineering, mathematics, or related Exp: Recent graduates |
As part of our Network development team, working on our master data management product (MDM), or as part of our Vault team, working on our Enterprise Content Management (ECM) product, you will be part of a team building scalable solutions that complement our existing solutions. In these exciting roles, you would have the opportunity to work with technologies like Java, Spring, Hibernate, Mule, Maven, Git, Tomcat, Solr, MySQL, and more. We work in a fast-paced, agile environment that releases features every four weeks. What You'll Do: Responsibility for all aspects of the software cycle: design, implementation, tuning, testing, and monitoring of the functional areas that you will own. etc. | 12/10/2019 |
| 12982 | Veeva Toronto, ON Associate Performance Engineer BS in computer science or related Exp: Recent graduates |
The Vault Performance Engineering Team works within the Vault Development Team and participates in all phases of the software development life cycle. What You'll Do: Test new features pre-production to make sure they will scale and perform. Collaborate with Vault team members in Product Management, Engineering Management and Quality Assurance to help design and develop performance tests. Implement and execute load tests in JMeter. Use and update Python scripts for managing test systems. Work with Senior Performance Engineers to profile code and identify bottlenecks. | 12/10/2019 |
| 12983 | Veeva Philadelphia, PA Associate Consultant (Remote) BA/BS in a business, computer, engineering, or life science field Exp: Recent graduates |
You will work on project teams implementing Veeva’s cloud software applications. Participate in business process discovery workshops, gather requirements, configure the solution, help with testing and final deployment. Explain solutions to a variety of audiences and provide subject matter expertise on Veeva applications and technical design. What You'll Do: Collaborate with experienced Senior Consultants and Solution Architects. Learn technical consulting, application design, industry knowledge and project management skills. Conduct solution design, application configuration, and documentation of system requirements to help deliver successful implementations. Passion to use technology to make business processes more efficient. etc. | 12/10/2019 |
| 12984 | Veeva Pleasanton, CA QA Engineer BS in mathematics or computer science Exp: 0-5 years |
Veeva Systems is looking for an energetic and enthusiastic Engineer to join our rapidly growing team. This is a hands-on position for delivering a quality SaaS product. As part of Veeva CRM Multi Channel software QA team, you will be given an opportunity to test a high quality product that was built from scratch. We are a fast-paced team who takes pride in building great software and making customers happy. What You'll Do: Design and implement test strategies. Develop deep expertise in the product. Build effective test cases that are used for manual and automation testing. etc. | 12/10/2019 |
| 12985 | Veracyte South San Francisco, CA Clinical Lab Scientist BS/MS in a biological science or medical technology Exp: 1 year |
The Veracyte Clinical Laboratory continues to grow! We are seeking a new Clinical Laboratory Scientist (CLS) to perform cutting-edge diagnostic testing on patient specimens in our collaborative, high-energy work environment. S/he will accurately perform molecular genetic testing, using a variety of molecular biological techniques including expression microarray analysis. Other key aspects of the role include: Conduct daily quantitative and qualitative assessment of molecular data generated during the course of testing. Carry out QC/QA activities as part of the company’s Quality program and commitment to patient safety. etc. | 12/10/2019 |
| 12986 | Vericel Cambridge, MA Engineer, Validation I MS Exp: 1+ year(s) |
Responsible for performing validation in a GMP biotech manufacturing facility. Core Responsibilities: Perform validation activities in the media preparation, cell culture, utilities and QC areas of a cGMP biotech manufacturing facility. Perform hands on execution of Installation, Operational and Performance Qualifications for equipment, facilities, utilities, as well as cleaning, sterilization, and manufacturing processes in accordance with predefined test protocols. Analyze validation results and compile data into reports for initial qualifications and re-qualifications. Coordinate testing schedule with impacted area managers and quality control based on project needs. Provide input to technical composition of standard operating procedures. etc. | 12/10/2019 |
| 12987 | Vericel Cambridge, MA Sales Operations Associate BS/BA in business administration, marketing, or related Exp: 1+ years |
Essential Functions: Coordinate on-boarding of all new sales personnel with internal departments. Administer all sales training content through company’s Learning Management System. Primary administrative resource for two sales teams (first point of contact). Provide logistical support for all sales training meetings and events. Work with marketing to provide regular updates to brand websites. Work with marketing to provide logistical support for tradeshows, surgeon training programs and other commercial programs/events. etc. | 12/10/2019 |
| 12988 | Verge Genomics South San Francisco, CA Molecular Biology Research Associate / Senior Research Associate MS in molecular biology, neuroscience, or equivalent Exp: 0+ years |
What you'll do: Perform and enable high-throughput sample processing and RNA extraction for transcriptomic analysis, which impacts all drug discovery and development efforts. Successfully conduct library prep of samples for RNAseq. Have the opportunity to learn across function and discipline, by contributing to ongoing studies and by utilizing techniques such as cell culture, high-throughput screening, plasmid preparation, virus preparation, IF, qPCR, or WB. Be responsible for evaluating and presenting your work at team and company level meetings. | 12/10/2019 |
| 12989 | Vero Biotech Atlanta, GA Manufacturing Technician Technical degree Exp: Not needed |
Routine Manufacturing operations for the production of clinical and/or commercial products, operation of production equipment according to SOPs and other daily activities on the manufacturing floor. Essential Duties and Responsibilities: Performs manufacturing activities including but not limited to work functions in electromechanical assembly and disposable assemblies (cassettes, cartridges) in a correct and timely manner. Maintains records and controlled-room environment to comply with regulatory requirements, GMPs, and SOPs. Provide in process testing to assure batches meet specifications. Will train personnel in new and revised procedures. etc. | 12/10/2019 |
| 12990 | Verve Therapeutics Cambridge, MA Associate Scientist, In Vivo Pharmacology MS in biology, biochemistry, pharmacy, or related Exp: 1-2 years |
Verve is seeking an Associate Scientist with experience in in vivo pharmacology to execute pivotal studies in rodents. You will be responsible for planning gene editing studies in mice and rats, dosing of animals (IV or IP), collecting blood samples (serial and terminal bleeds), necropsy and tissue harvesting. In addition, you will be analyzing the collected samples using a series of ex vivo and in vitro assays. The role requires hands-on experience in rodent handling, dosing and sampling as well as the ability to develop and run assays such as ELISA, qPCR or FACS. The scientist in this position will be part of an integrated R&D project team. | 12/10/2019 |
| 12991 | MRIGlobal Kansas City, MO Electrical Engineer MS in eletrical/electronics engineering Exp: 0-3 years |
MRIGlobal has an exciting full-time opportunity for an Associate Electrical Engineer in our Intelligence, Surveillance, and Reconnaissance Division located in Kansas City, MO. In this unique opportunity, the selected candidate will work with other engineering and technical disciplines in the design, prototyping, and testing of custom systems to meet customer requirements. Furthermore, the selected candidate will: Design a broad range of analog and digital circuits, Design and layout custom circuit boards to meet challenging packaging and performance requirements, etc. | 12/9/2019 |
| 12992 | Merck KGaA Verona, WI Associate Production Scientist BS in Chemistry, Biochemistry, Chemical Engineering, or equivalent Exp: <1 year |
Position primarily involves the safe and efficient manufacturing of API’s according to cGMP requirements. Kilo Lab and Pilot Plant manufacturing of APIs and intermediates. Demonstrate proper lab safety practices, and work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines. Maintain the safety and cleanliness of production areas and all related equipment during each shift, specifically potent compound handling techniques | 12/9/2019 |
| 12993 | Merck KGaA Billerica, MA Research Associate - Protein Expression Bachelor’s degree in Biology, Microbiology or other related Science Exp: <1 year |
We are seeking a motivated researcher to join our recombinant protein expression team at EMD Serono. The Operations group, as part of the Protein and Cell Sciences (PCS) department, generates micrograms to grams of purified protein. The successful candidate will primarily be responsible for small and large scale expression of therapeutic and reagent proteins primarily by transient transfection of mammalian cells lines or from stable cell lines to support preclinical research. The incumbent would also be responsible for maintaining expression cell lines, cell passaging, generating stable mammalian cell lines, selection of high expressing cell lines, creation of research cell banks, optimizing cell growth and protein expression. | 12/9/2019 |
| 12994 | Merck KGaA Oakland, CA Field Service Engineer - Northern CA HS Diploma/GED Exp: 1+ year in field service/mechanics |
In the role of Field Service Engineer (FSE), you will be responsible for the installation, repair, preventative maintenance and qualification of water purification systems throughout Northern CA (Oakland/North Bay/Richmond/Walnut Creek) area. You will also be responsible to provide backup support to nieghboring territoriess as required. | 12/9/2019 |
| 12995 | Merck KGaA St. Louis, MO Packaging Operator I HS Diploma/GED Exp: 3+ months in ISO/GMP environment |
To stage, fill (manually or semi-automatically), cap, label, and over pack liquid, powder, and lyophilized products per approved packaging specifications. Clean laboratory glassware and batch tanks. Complete appropriate packaging documentation per FDA, ISO, and GMP procedures and deliver products to inventory. Assemble and package chemical kits. Fill, cap, and label chemical products. Manually fill liquids or powders. Utilize semi-automated equipment to fill liquids or powders. Fill products utilizing aseptic techniques. Perform fills in environmentally controlled areas. Fill hazardous products. Transfer bulk utilizing peristaltic pumps. Filter bulk materials using pumps and in-line filters or vacuum filters. Operator automated and semi-automated cappers. Manually torque caps with wrenches | 12/9/2019 |
| 12996 | Merck KGaA Rockville, MD Flexible Resource Associate Scientist BS or MS in sciences Exp: BS: 1+ years, MS: 0 years |
The Flexible Resource Associate Scientist is a dynamic contributor with an opportunity to work in many different laboratories. You will conduct important assays by making scientific observations, maintaining detailed workbooks, and documenting to GLP/GMP standards. Deployment duration and the specific laboratory and will be coordinated via the Sales and Operations Planning (S&OP) process. | 12/9/2019 |
| 12997 | Merck KGaA Springfield, MA Research Engineer, Life Sciences BS or MS in Mechanical, Electrical, Bioprocessing, Biochemical or Biomedical engineering Exp: <1 year |
You will be working in the life sciences group focusing on the development of the acoustic affinity cell selection platform. You will work on all aspects of the early stages of new product development, i.e., brainstorming, concept selection, engineering design and analysis, prototype assembly, testing and documentation. You will perform acousto-fluidic affinity cell selection experiments participate in design of experiments. You will take on SOP writing and lab management duties as needed to enable the team to maintain a fast and steady flow of experiments. You will develop into an independent thinker, innovator and contributor to the development of the cell selection platform. | 12/9/2019 |
| 12998 | Merck KGaA St. Louis, MO cGMP Associate Production Scientist BS/BA in chemistry, biochemistry, biology, chemical engineering or related Exp: <1 year |
The cGMP Associate Production Scientist is responsible for the manufacturing of active pharmaceutical ingredients (APIs) Chemicals and bulk pharmaceuticals regulated by the Food and Drug Administration (FDA). They are responsible for following manufacturing protocols, consistent with and established according to current Good Manufacturing Practices (cGMP), and ensuring the accuracy of documentation. | 12/9/2019 |
| 12999 | Miltenyi Biotec Gaithersburg, MD Manufacturing Associate - Upstream and Downstream BS/BA Exp: 0-2 years in GMP setting |
The qualified candidate will be responsible for adhering to GMP’s by following Standard Operating Procedures and executing Batch Production records using good documentation practices. Your exceptional ability to perform aseptic processes in a GMP cleanroom environment will contribute to the manufacture of lentiviral vectors used in human clinical trials, and propel Lentigen Technology’s continued growth and success. | 12/9/2019 |
| 13000 | Micr Indianapolis, IN Medical Research Coordinator Associate: BS/BA Exp: 1-3 years clinical research experience preferred |
We are seeking an experienced individual who has been involved in clinical research. 1-3 years of clinical research experience is preferred for this full-time position. | 12/8/2019 |
| 13001 | LabCorp Monrovia, CA Histotechnician - (3rd Shift) AS/AA in related Exp: 1-3 years in Histology |
The Monrovia lab is seeking a 3rd shift Histotechnician for the Histology department. This position will perform all technical duties related to the production of histo-pathological slides including but not limited to the following: Examines and prepares histologic slides from tissue sections for microscopic examination and patient diagnosis. Uses rapid tissue processing and frozen section technique to freeze, cut, mount, and stain tissue specimen received from surgery, biopsy, and anatomical tissues upon preparation of sections of human or animal tissue for immediate examination. Operates computerized laboratory equipment to fix, dehydrate, and infiltrate with wax, tissue specimens to be preserved for study by Pathologist. | 12/8/2019 |
| 13002 | LabCorp Utica, NY Specimen Processing Specialist (Laboratory Associate) HS Diploma/GED Exp: 1 year in lab |
Prepare laboratory specimens for analysis and testing, Spin samples, pour urine tubes, and create frozen samples, Pick up and deliver samples to, clients/hospitals, Unpack and route specimen to their respective staging areas, Accurately identify and label specimens, Pack and ship specimen to proper testing facilities, Properly prepare and store excess specimen samples | 12/8/2019 |
| 13003 | LabCorp Raritan, NJ Lab Assistant - 3rd Shift HS Diploma/GED Exp: 1 year in health-related work or college level courses in lab sciences |
The Forensic Accessioning (Processing) Lab Assistant works in fast paced, production type environment performing a vital component of medical laboratory science. Receive on the job training for the pre-analytical processing of medical samples. Complete all documents accurately and neatly. Monitor chain of custody, and custody and control forms for completeness and acceptability. Perform all duties accordingly to standard operating procedures and/or supervisory instructions | 12/8/2019 |
| 13004 | LabCorp Richmond, VA Specimen Accessioner HS Diploma/GED Exp: 0-2 years related experience |
Prepare laboratory specimens for analysis and testing, Spin samples, pour urine tubes, and create frozen samples, Pick up and deliver samples to, clients/hospitals, Unpack and route specimen to their respective staging areas, Accurately identify and label specimens, Pack and ship specimen to proper testing facilities, Properly prepare and store excess specimen samples | 12/8/2019 |
| 13005 | LabCorp Huntsville, AL Technologist BS/BA in biology, chemistry, med tech, or related Exp: 1 year clinical lab experience |
Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation. Demonstrate the ability to make technical decisions regarding testing and problem solving. | 12/8/2019 |
| 13006 | LabCorp Oklahoma City, OK Laboratory Data Entry/Specimen Accessioner HS Diploma/GED Exp: 1-2 years in data entry |
Our LabCorp office in Oklahoma is expanding its team and looking for dynamic individuals to be Specimen Accessioner (s) who will perform specimen preparation duties. Their work involves receiving and unpacking specimens, preparing them for lab tests and ensuring that they are correctly preserved before they are sent off. | 12/8/2019 |
| 13007 | LabCorp McLeansville, NC Customer Service HS Diploma/GED Exp: 1-3 years in call center/customer service |
Customer Service- FT 10-7pm OR 11-8pm- Work from Home Opp-Onsite needed first! Answer 70+ inbound calls per day from patients, doctor's office and/or private insurance carriers. Initiate payment plans for patients for outstanding balances. Maintain telephone statistics and quality goals | 12/8/2019 |
| 13008 | Medtronic Danvers, MA Associate Regulatory Affairs Specialist - Coronary and Structural Heart BS/BA in biology, chemistry, med tech, or related Exp: 0 years in medical device |
The Associate Regulatory Affairs Specialist (ARAS) is responsible for planning and executing global regulatory activities necessary to obtain and maintain regulatory approvals within the US and International Regions. The Regulatory Affairs Specialist will provide support for regulatory activities including: technical writing to support regulatory submissions, product labeling and instructions for use creation. | 12/8/2019 |
| 13009 | Medtronic North Haven, CT Manufacturing Engineer I BS/BA Exp: 0 years |
The Associate Manufacturing Engineer is a key operations representative within the Advanced Stapling Technology Manufacturing Engineering team. The Associate ME will be responsible for completing tasks which support the completion of operations deliverables for AST Focused Factory. General responsibilities include manufacturing process evaluation, mechanical product troubleshooting and support of in-house manufacturing processes. They will assist with engineering studies to support process validation and contribute to maximizing production performance. The Associate ME will work under the direction of Principal/Senior level Engineer in a fast paced collaborative environment supportive of program initiatives and compliant with company best practices. | 12/8/2019 |
| 13010 | Medtronic Memphis, TN R&D Engineer II MS in engineering Exp: 0 years |
This position has the responsibility and authority to apply education and learned knowledge toward developing world class medical products for Spinal surgery. Designs, develops, analyzes, troubleshoots and provides technical skills during research and/or product development. Uses multidisciplinary engineering knowledge to design and develop medical devices or components / subsystems in support of strategic plans. | 12/8/2019 |
| 13011 | Medtronic Tempe, AZ IC Test Engineer I BS/BA in electrical/computer engineering Exp: 1-2 years in circuit testing/design/verification |
As a member of this Test Engineering Team, you will be involved in all phases of product development, including definition, design for testability, test hardware and software design, hands-on debug, characterization, manufacturing release under a heavily regulated quality and regulatory standard operating procedures. You will be an important part of an experienced test development team whose goal is to deliver the highest quality test application to test ICs for use in live saving medical devices | 12/8/2019 |
| 13012 | Medtronic Memphis, TN Assoc Supplier Qual Engineer BS in engineering/sciences Exp: 0 year of work |
Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. | 12/8/2019 |
| 13013 | Medtronic Irvine, CA Design Quality Engineer I BS in engineering/sciences Exp: 0 years in quality/engineering |
Applies knowledge of Design Control principles and quality engineering techniques positively influence new product development efforts, including those for design verification, validation, specification development, and risk management. Hands on participant in early stages of product development including but not limited to physician interaction, product engineering, competitive product testing, and prototype testing. Identifies and manages risk throughout the development process with the use of FMECA and/or other risk management tools. | 12/8/2019 |
| 13014 | Medtronic Jacksonville, FL Supplier Qual Engineer I BS/BA Exp: 0 years |
The Restorative Therapies Group (RTG) develops life-restoring therapies and healthcare solutions that span the care continuum; integrating technologies and applying clinical and economic evidence to increase patient access, improve efficiency of procedures and deliver successful patient outcomes. Within RTG the Supplier Quality department focuses on developing Supplier Owned Quality (SOQ). This is a process allowing suppliers to use portal system in which supplier data is electronically transmitted to Medtronic via an Internet or secure FTP port. The portal system provides real-time material acceptance confirmation, shipment authorization and feedback to supplier prior to release of the product and identifies opportunities to reduce variation in the process. It also reduces the burden on Incoming Quality Assurance. | 12/8/2019 |
| 13015 | Merck West Point, PA Associate Scientist, Vaccine Process Development BS in engineering or biological sciences Exp: 2020 graduate |
The successful candidate will perform lab-scale process development/scale-up studies, develop robust, efficient, scalable cell culture processes for vaccine production, participate in the manufacture of Current Good Manufacturing Practices (CGMP) clinical bulks, and transfer processes to clinical or commercial manufacturing facilities for vaccine candidates. Duties may include: lab scale fermentation, cell culture, and/or bioconjugation process development, in-process assay support, process scale-up and engineering, CGMP document preparation and modifications, maintaining/coordinating raw material, and equipment inventories, technology transfer to manufacturing, and functioning as a key member of a process development team. | 12/8/2019 |
| 13016 | Merck West Point, PA Associate Shift Engineer BS in engineering or sciences Exp: 1 year |
The function of this position is to provide technical support for ourfacility while actively supporting, participating in, and embracing an empowered culture. This role is for Off-Shift Engineering Support (3rd shift Monday through Friday). Specifically, the position will be required to: Provide on-the-floor support of operational and technical issues; collaborating with the shop floor to provide immediate responses to deviations and potential deviations. Performing deviation investigations aimed to prevent deviation re-occurrence, including determining the root cause, identifying corrective/preventative actions, identifying event scope, and conducting a product impact assessment. Where applicable, complete investigational test protocols to determine root cause, product impact, event scope, etc | 12/8/2019 |
| 13017 | Merck Elkhorn, NB Technician, Operations HS Diploma/GED Exp: 1-2 years in production lab |
The Operations Technician is responsible for critical laboratory procedures and duties in the production of veterinary products. Technicians work with a variety of technical equipment while completing duties involved in blending, filling vials or packaging finished products for distribution. At all times technicians must follow Good Manufacturing Practices and Standard Operating Procedures (SOP) and adhere to all safety and company policies while performing assigned duties. | 12/8/2019 |
| 13018 | Merck West Point, PA Shift Engineer BS in engineering Exp: 1 year |
The function of this position is to provide technical support for our facility while actively supporting, participating in, and embracing an empowered culture. This role is for Off-Shift Engineering Support (2nd Shift Monday through Friday). Specifically, the position will be required to: Provide on-the-floor support of operational and technical issues; collaborating with the shop floor to provide immediate responses to deviations and potential deviations.Performing deviation investigations aimed to prevent deviation re-occurrence, including determining the root cause, identifying corrective/preventative actions, identifying event scope, and conducting a product impact assessment. Where applicable, complete investigational test protocols to determine root cause, product impact, event scope, etc | 12/8/2019 |
| 13019 | Merck Ames, IA Technician, Operations AS/AA in biology, microbiology, or related Exp: |
The primary purpose of this position is to perform entry-level laboratory procedures and assist others in more advanced procedures for the production of veterinary biologicals according to strict government and company imposed guidelines. Assist in all areas of the production of RNA (RP) Particle Vaccine products manufactured in a USDA licensed facility. | 12/8/2019 |
| 13020 | Merck North Wales, PA Entry Level Field Sales - Chronic Care - (Forest Hills, NY) BS/BA Exp: Entry level, some sales experience |
The entry level Chronic Care Representative (CCR) is the primary point of contact for a variety of customers within their assigned geography. The Chronic Care Representative is a key member of the local Customer Team that works collaboratively with other Company field-based employees such as the Account Executives, Integration Delivery Systems leaders as well as other members of the extended team. Professionals to align customer needs and Company products in accordance with product labeling. | 12/8/2019 |
| 13021 | Merck West Point, PA Entry Level Field Sales - Vaccines -Chico, CA BS/BA Exp: Entry level, some sales experience |
He/she is responsible for engaging with customers in a way that supports the local market focus on population health and centers on the highest potential business opportunities that will improve our impact on public health. He/she will work with the local market team to understand and identify customer needs, proactively align products and services, support pull-through activities relative to integrated strategies, and ensure that MV is viewed as demonstrating value and better health outcomes to healthcare professionals and their patients. Responsible for ensuring all activities adhere to the spirit and letter of all Company Policies and US Laws and Regulations. | 12/8/2019 |
| 13022 | Meridian North Billerica, MA Clinical Research Associate - MAG BA/BS in biological/health sceinces Exp: 1 year as CRA |
The Clinical Research Associate assists in the administrative of clinical research projects including development of key study documents, over-site of the clinical trial, and ensuring the quality and integrity of the data according to GCP, ICH and SOPs. Interact with data management and study sites with generation and reconciliation of queries in order to meet business timelines. Provide answers to common protocol study related questions under the supervision of the Clinical Director or Associate Trial Manager | 12/8/2019 |
| 13023 | Meridian Cincinnati, OH Quality Systems Software Engineer BS/BA in Communications, Computer Systems, or equivalent Exp: 0-2 years related experience |
The Quality Systems Software Engineer position at Meridian Bioscience within the Quality Assurance department supports the Quality System by developing and maintaining electronic document and data management systems. The Quality Systems Software Engineer works with cross functional teams to identify areas that can be streamlined or improved by implementing processes that meet regulatory requirements and standards associated with electronic data management. The Quality Systems Software engineer.is responsible for application systems administration within the scope of Quality Systems. This includes developing electronic form records, document management and workflow processes, and authoring supporting documentation including but not limited to validation protocols and reports and verification test methods and procedures. | 12/8/2019 |
| 13024 | Merieux NutriSciences Madison, WI Entry-Level Laboratory Sample Receiving Technician HS Diploma/GED Exp: Entry Level |
We are looking for an Entry-Level Laboratory Sample Receiving Technician to sit in our Madison, WI location. Receive and log in sample in preparation for analysis. Review sample and any attached documentation to assign an identification number and enter information into Laboratory Information Management System (LIMS). Prepare documentation as necessary. Contact client, when necessary, to obtain and clarify missing or unclear information to ensure that identification of client code, test code, and sample contents are accurate. Store sample in appropriate manner until analysis is completed and appropriately dispose of extra sample. Ensure sample integrity is maintained. | 12/8/2019 |
| 13025 | Merieux NutriSciences Crete, IL RESEARCH MICROBIOLOGIST AS/AA or BS/BA in chemistry/biology Exp: 1-2 years |
This position is responsible for working in a cooperatively team environment where scientists collaborate on contract research designed to promote the safety, quality and nutrition of the global food supply. The incumbent is responsible for the testing of samples supporting research studies using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. The incumbent contributes to defined contract research projects by performing lab tests, data interpretation and maintaining documentation in accordance with required specifications, established procedures, and customer service standards. | 12/8/2019 |
| 13026 | Merieux NutriSciences Crete, IL CHEMIST I BS/BA in chemistry Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. This position reports to the Supervisor of Chemistry. Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. | 12/8/2019 |
| 13027 | Merieux NutriSciences Allentown, PA Lab Assistant HS Diploma/GED minimum Exp: No experience needed |
Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. | 12/8/2019 |
| 13028 | Merieux NutriSciences Columbus, OH Micro Tech HS Diploma/GED minimum Exp: No experience needed |
Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. | 12/8/2019 |
| 13029 | Merieux NutriSciences Grand Prairie, TX Microbiology Technician BS/BA Exp: 1 year of PCR/ELISA experience |
The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 12/8/2019 |
| 13030 | Merieux NutriSciences Salida, CO Micro Tech HS Diploma/GED minimum Exp: No experience needed |
Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. | 12/8/2019 |
| 13031 | MeritMedical South Jordan, UT Process Operator Wafer I HS Diploma/GED Exp: 6 months in silicon wafer fab. Preferred |
This position is for a Process Operator Wafer I at Merit Sensor Systems. Merit Sensor Systems is a manufacturer of piezoresistive pressure sensors (learn more at www.merit-sensor.com). This Process Operator Wafer I could be working in the wafer fabrication, wafer dicing, and/or electronic assembly areas. | 12/8/2019 |
| 13032 | MeritMedical South Jordan, UT Material Handler I / with a $500 Hiring Bonus HS Diploma/GED Exp: 3 months work experience |
Responsible for pulling parts from the warehouse and seeing that line production workers have the raw materials they need to perform their jobs. Obtains parts from the warehouse for use in production and verifies the part's lot number to ensure that the proper materials are used. Pulls supplies for assembly workers and ensures that supplies are stocked and readily available for assembly workers. | 12/8/2019 |
| 13033 | MeritMedical South Jordan, UT Molding Technician I - Day Shift HS Diploma/GED Exp: 6 months molding experience |
This position provides entry level mold set-up services under the direction and supervision of a Technician and/or Supervisor. Assists in mold changes and EOAT setup/verification. Assists in set up of all auxiliary equipment related to the process. Ensures that correct materials are utilized, safety checks are performed, and that room organization and cleanliness is maintained. | 12/8/2019 |
| 13034 | MeritMedical South Jordan, UT Technician II (Injection Molding) AS/AA Exp: 1 year |
Performs routine technical tasks including assembling or constructing simple or standard equipment or parts in an injection molding environment, and may service or repair simple instruments or equipment. Prepares test specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Extracts engineering data from various prescribed sources and processes the data following well-defined methods, then presents the data in prescribed form. | 12/8/2019 |
| 13035 | MeritMedical South Jordan, UT Accounts Payable Clerk I HS Diploma/GED Exp: 1 year |
This position provides accounting support for processing employee expense reports, maintaining the filing system, processing the daily customer checks and maintaining the Construction Work in Progress (CWIP) filing system. | 12/8/2019 |
| 13036 | MeritMedical South Jordan, UT Production Operator II - Part Time HS Diploma/GED Exp: 6 months experience preferred |
Performs a variety of medical assembly and processing tasks as a production team member. Assembles medical products on an assembly operation, performing a variety of tasks on a rotating basis. Performs on-line and in-process visual inspection of products to ensure specifications per work order and procedure are followed. Assists Team Leader and Technicians with product and/or machine change-overs | 12/8/2019 |
| 13037 | MeritMedical South Jordan, UT Material Handler I HS Diploma/GED Exp: 3 months work experience |
Responsible for pulling parts from the warehouse and seeing that line production workers have the raw materials they need to perform their jobs. Obtains parts from the warehouse for use in production and verifies the part's lot number to ensure that the proper materials are used. Pulls supplies for assembly workers and ensures that supplies are stocked and readily available for assembly workers. | 12/8/2019 |
| 13038 | Merz Franksville, WI Supply Chain Associate BS/BA Exp: 1-3 years work or intern experience in supply, manufacturing, or quality |
The individual will be involved with people and processes associated with various aspects of Supplier Management and Procurement at Merz. The successful candidate will implement the supplier selection and approval process; manage existing suppliers; place purchase orders (PO’s); evaluating supplier performance; resolve delivery issues; assess and reduce supply chain risk; save money by reducing TCO (total cost of ownership). | 12/8/2019 |
| 13039 | Merz Franksville, WI Tech Ops Development Associate BS/BA in engineering, sciences, business or communications Exp: Entry |
As a member of Merz’s Technical Operations Development Program, you will have three assignments over the course of three years. The roles are crafted to help you develop exceptional functional and leadership traits by working on a wide range of projects while providing exposure to different leaders in the company. These Operational experiences will develop you and put you on the fast track to future operations leadership opportunities at Merz. | 12/8/2019 |
| 13040 | MSD Gaithersburg, MD Research Associate I, Immunoassay Development BS in life sciences, chemical sciences, MS preferred Exp: 1 year in assay development |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. | 12/8/2019 |
| 13041 | MSD Rockville, MD Production Control Tech I BS in life sciences, chemical sciences, MS preferred Exp: 1 year in biotech lab/manufacturing |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. The position will help standardize and improve documentation, manufacturing procedures and processes to increase production efficiency and ensure best practices are followed. The position will also help implement new products, projects and processes within Manufacturing Operations. Some degree of professional latitude, creativity and self-management is expected. | 12/8/2019 |
| 13042 | MSD Rockville, MD Customer Service Rep I BS/BA Exp: 1 year in customer support |
The Customer Service Representative I will provide professional, courteous, customer-centric service to the MSD customer base. This individual will directly interact with various customers and interface with multiple internal departments to facilitate the processing of quotes, orders and customer requests to allow for timely shipping of MSD products worldwide. | 12/8/2019 |
| 13043 | MSD Rockville, MD Customer Service Rep I BS/BA Exp: 1 year in customer support |
The Customer Service Representative I will provide professional, courteous, customer-centric service to the MSD customer base. This individual will directly interact with various customers and interface with multiple internal departments to facilitate the processing of quotes, orders and customer requests to allow for timely shipping of MSD products worldwide. | 12/8/2019 |
| 13044 | MSD Gaithersburg, MD Research Associate I, Immunoassay Development BS in life sciences, chemical sciences, MS preferred Exp: 1 year in assay development |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. | 12/8/2019 |
| 13045 | MSD Gaithersburg, MD Research Associate I, Immunoassay Development BS in life sciences, chemical sciences, MS preferred Exp: 1 year in assay development |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. | 12/8/2019 |
| 13046 | Analytical Lab Group Concord, CA QA Assistant BS in sciences Exp: 0-2 years in pharma/biotech |
The main duties of the Quality Assurance (QA) Assistant are to ensure timeliness of testing, meeting client requirements and providing a safe work environment for employees. The QA Assistant must provide services that are compliant to the ALG-West Quality Manual, client requirements and regulatory requirements as applicable, including ISO/IEC 17025:2017, USP, EU, GLP, GMP, FDA and ICH guidelines. | 12/8/2019 |
| 13047 | Analytical Lab Group Concord, CA EM Technician AS/AA Exp: 0-2 years in cleanrooms |
Analytical Lab Group is looking for laboratory technicians to perform environmental monitoring at client facilities and microbiology testing in the microbiology lab. This is a full-time position at our West Coast location. The schedule will be Monday-Friday, 7 a.m. to 3:30 p.m., but you must be able to work flexible hours, including different shifts and weekends. At this time, the starting hour is 5 a.m. and will require OT. | 12/8/2019 |
| 13048 | Micropoint Santa Clara, CA Quality Control Associates MS in chemistry, biology or related Exp: 0-2 years |
We are looking for highly motivated QC Associates (two openings) to join our quality team. These positions are responsible for participating as team members in a laboratory environment for finished product/or development programs focused on the goal of testing and releasing the immunoassays found in Micropoint's in-vitro diagnostic products for point-of-care (POC) testing. | 12/8/2019 |
| 13049 | Micropoint Santa Clara, CA Manufacturing Operators HS Diploma/GED Exp: 0-2 years in pharma/food/med manufacturing |
There are two openings. These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the company's disposable test cartridges. Follow written procedures for set-up, operation, and clean up of manufacturing equipments, final assembly, and packaging. Responsible for manual tasks including, pipette solution, pouch and box labeling, product inspection. Prepare materials used in the cartridge production process | 12/8/2019 |
| 13050 | Micr Indianapolis, IN Medical Research Study Coordinator: BS/BA Exp: 1-3 years clinical research experience preferred |
We are seeking an experienced individual who has coordinated the implementation of clinical research protocols. 1-3 years of clinical research experience and CCRC certification is preferred for this full-time position. | 12/8/2019 |
| 13051 | T2Biosystems Lexington, MA Research Associate, Molecular Assay Development BS in biology, biochemistry, or related Exp: 0-2 years |
As a motivated, curious and goal-oriented research associate, you will join a dynamic R&D team and contribute towards the development of novel molecular methodologies and assays for diagnostic applications. You will execute studies, conduct data analysis, and document results. As a contributor you will interact with other individuals and groups across our research and product development teams. You must have strong communication, analytical and quantitative skills and thrive working with highly skilled teams on multiple, simultaneous projects in a fast-paced technical setting. etc. | 12/4/2019 |
| 13052 | T2Biosystems Lexington, MA Research Associate - Process Development BS/MS in biology, biochemistry, biotechnology, or related Exp: 1-2 years |
We are seeking a talented and highly motivated individual to join our multi-disciplinary team as a Research Associate. This individual will be a key contributor to executing reagent formulation activities including technology transfer, process development, analytical method development, verification and validation. The position will be located in Lexington, MA. Responsibilities: Development, optimization, scale up, and validation of reagent processes and measurement systems; including DOE and capability analysis. Experimental planning, execution, and data analysis. etc. | 12/4/2019 |
| 13053 | T2Biosystems Lexington, MA Research Associate /Research Associate II - Microbiology (Contract to Perm) BS/MS in molecular biology or related Exp: 0-3 years |
This position is to fill a need within our Microbiology group working in our Lexington, MA location. The RA will provide aid in the development of laboratory protocols for the cultivation and characterization of pathogenic organisms. The individual will work with the T2 Microbiology staff to expand on our established protocols and methods to enable the accurate production of test samples for development of novel assays in conjunction with the Assay Development group. This role consists of hands-on execution in the laboratory and data analysis within the Microbiology group. etc. | 12/4/2019 |
| 13054 | Talis Biomedical Menlo Park, CA Research Associate MS in biology, microbiology, molecular biology, biochemistry or related Exp: 0-3 years |
The candidate will join the Assay Development group in the R&D division where focus is on molecular assays development such as nucleic acid isolation, purification, amplification and labeling technologies. We are seeking talented, motivated individuals to join a collaborative effort to enable development of rapid diagnostic tests of several pathogens from various clinical specimens. Position Responsibilities: Work with senior scientists and run hands-on experiments for microbiology, sample preparation, nucleic acid extraction and amplification. Participate in design of molecular assays. etc. | 12/4/2019 |
| 13055 | Talis Biomedical Menlo Park, CA Test Engineer - Embedded Software & Firmware BS in an engineering field Exp: 0-4 years |
Position: Learn and develop expertise on our firmware and embedded software requirements, in order to create automatable test scripts. Author basic functionality, stress, and reliability tests using state-of-the art tools, and novel in-house test fixtures. Document and perform root cause analysis on testing failures. Collaborate closely and clearly communicate test plans and results to cross-functional team members. Other duties as assigned. | 12/4/2019 |
| 13056 | Tango Therapeutics Cambridge, MA Associate Scientist, Immunology BS/MS in immunology or related Exp: 0-8 years |
We are seeking an innovative, collaborative and enthusiastic immunologist to work on building our immunology and Immuno-Oncology Programs. This individual will work primarily at the bench to help drive target identification, validation, and patient selection strategies. Job Responsibilities: Culture and engineer primary human T cells and murine T cells using genetic tools. Culture and engineer primary human tumor cell lines and murine cell lines using genetic tools. etc. | 12/4/2019 |
| 13057 | TCR2 Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Analytical Process Development BS in biochemistry, cell biology, immunology or related Exp: 1-2 years |
Responsibilities: Learn and execute on all assays used by the analytical team (qPCR, ELISA, T-cell based assays). Assist in the analysis and characterization of lentiviral vectors for use by multiple internal research groups. Work with process development teams to investigate, improve, and implement advanced vector production processes. Analyze results, solve problems, and troubleshoot assays. Participate in assay development of established analytical tools and help develop new assays. Develop and maintain various cell lines used in cell-based analytical assays. etc. | 12/4/2019 |
| 13058 | TCR2 Therapeutics Cambridge, MA Research Associate, Vector Production BS/MS in molecular biology, biochemistry, protein chemistry, or related Exp: 1-2 years |
Responsibilities: Generation and maintenance of various cell lines and used by internal research groups. Production of retroviral vector stocks using various transfection methodologies. Assist analytics team in evaluation of in-process and endpoint samples. Thorough documentation of procedures and experiments. Coordinate with various internal groups for the generation and evaluation of emerging vector products. Assist in drafting of SOPs, technical documents, batch records, etc, for transfer to external CMOs. Participation in internal and external meetings detailing ongoing work. etc. | 12/4/2019 |
| 13059 | TE Connectivity Manfield, OH Electrical Engineer BS in physics or electrical or mechanical engineering Exp: 0-1 years |
TE Connectivity’s R&D/Product Development Engineering Teams conceive original ideas for new products, introduce them into practice. They are responsible for product development, and qualification from market definition through production and release; assist in the qualification of suppliers for new products to ensure suppliers deliver quality parts, materials, and services for new or improved manufacturing processes; conduct feasibility studies, testing on new and modified designs; direct and support detailed design, testing, prototype fabrication and manufacturing ramp. The R&D/Product Development Engineering Teams provide all required product documentation including, but not limited to, Solid Model, 2D/3D production drawings, product specifications, and testing requirements. They create and modify detailed drawings and drafting or conceptual models from layouts, rough sketches or notes and contribute to design modifications to facilitate manufacturing operation or quality of product. etc. | 12/4/2019 |
| 13060 | TechLab Blacksburg, VA Research Technician BS in a life science Exp: 1 year |
TechLab, Inc. develops, manufactures and distributes medical diagnostic tests. Our company places emphasis on science and collaboration with Universities. We are hiringa Research TechnicianforourScientific Affairs teams.The Research Technicianwill aidthe team with experiments and research. The Research Technician can be expected to perform protein purification using chromatography, write Standard Operating Procedures and Master Batch Records, and assist with assay development and optimization. etc. | 12/4/2019 |
| 13061 | Tecomet Warsaw, IN Material Associate HS diploma or equivalent Exp: 1-3 months |
The Material Associate will receive, unpack, verify, and store raw materials. Issue raw material to job routers and deliver to appropriate work areas. Maintain movement of subcontract production parts returning from vendors. This is accomplished by maintaining Tecomet principles of Safety, Quality, Customer Satisfaction and Innovation. Essential Duties and Responsibilities: Receive raw material and out-vend production parts and enter receipt into computer. Receive delivery of UPS, Fed-Ex and other transportation carriers and document receipt in computer. Issue raw material to specific job routers and deliver to specific production unit.Document receipt in computer. Perform weekly cycle-counting to ensure material counts are correct. etc. | 12/4/2019 |
| 13062 | Tempus , MI Account Associate BS in a life science, business, or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). Coordinating Medical Affairs report review with physicians after clinical orders. Order Kit and literature replenishment at accounts. Identifying and attending approved local conferences. Working with accounts to obtain necessary clinical data / progress notes for Tempus-tested patients. etc. | 12/4/2019 |
| 13063 | Tempus Chicago, IL Clinical Molecular Technologist MS in medical technology, clinical laboratory science, or related science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. Work our daytime shift Monday - Friday. | 12/4/2019 |
| 13064 | Tempus Chicago, IL Clinical Molecular Technologist (Shift Diff - Tuesday to Saturday) MS in medical technology, clinical laboratory science, or related science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. Work our daytime shift Monday - Friday. | 12/4/2019 |
| 13065 | Tempus Chicago, IL Clinical Molecular Technologist (Sunday-Wednesday with Shift Diff.) MS in medical technology, clinical laboratory science, or related science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. Work our daytime shift Monday - Friday. | 12/4/2019 |
| 13066 | TeVido BioDevices Austin, TX Biotech Manufacturing Technician AS/BS in biological sciences or engineering Exp: 0-1 years |
TeVido BioDevices is seeking a highly motivated individual to join our team as a Biotech Manufacturing Technician. We are a small Austin, TX-based biotech company that is addressing unmet needs in reconstructive and cosmetic surgery. The company has launched the manufacturing of our first product, cellular grafts, to treat patients with skin pigmentation disorders such as vitiligo. The person in this role will be responsible for performing daily production operations, including processing, quality control tests, and production facility cleaning; documenting work; and aiding improvement projects. This individual should be detail-oriented and self-motivated. An Associate’s degree in biological sciences or bioengineering and experience with aseptic technique in a laboratory or cleanroom is required. This is a challenging and exciting opportunity to contribute to an innovative, fast-paced startup in Austin, TX whose mission is to enhance patients’ quality of life using their own tissue. etc. | 12/4/2019 |
| 13067 | Thermalin Cleveland, OH Research Associate-Protein Formulation MS in biochemistry or related Exp: 1 year |
Thermalin is looking for a Research Associate – Protein Formulation to join our team. In this role, you will formulate insulin analogs for preclinical development. Research Associate Responsibilities: Formulate novel insulin analogs using established protocols. Quantify insulin analogs using reverse-phase (RP) analytical chromatography. Characterize insulin formulations with novel excipients using various biochemical methods. Develop new formulation schemes for insulin analogs. Optimize procedures and protocols to improve throughput. Perform laboratory tasks safely, rapidly, and efficiently. Report results in written and verbal format. Record results accurately and meticulously. | 12/4/2019 |
| 13068 | ThermoFisher Scientific Greenville, NC Formulation Technician II HS diploma/AS Exp: 1 year |
How will you make an impact? Sets-up, operates, and maintains the classified environments and manufacturing equipment for pharmaceutical products. Ensures operations are performed in a safe and responsible manner striving to create an injury-free and incident free workplace. What will you do? Operation of aseptic filling, freeze drying and capping equipment. Ensures pharmaceutical products in manufacturing are in accordance to SOPs and current GMP and other batch related activities. Verifies and documents production activities in batch records, logbooks, etc. Assists in troubleshooting operational and production problems in order to identify appropriate corrective actions. Performs the disassembly, assembly, cleaning, and operation of area manufacturing equipment. etc. | 12/4/2019 |
| 13069 | ThermoFisher Scientific , IL Field Service Technician BS in engineering, biology, chemistry, or related Exp: 1+ years |
The Field Service Technician (FST) performs planned maintenance, repairs and other verification/qualification services on a variety of laboratory instruments in assigned territory. The FST engages with customers and provides basic instrument services in a professional and timely manner. Essential Functions: Provides planned maintenance (PM), basic repair services and temperature verifications. Displays professionalism, understanding, tact, fairness and technical knowledge in all customer interactions. Follows all reporting responsibilities of Remote Service Dispatch (RSD), Escalation, Field Problem Report (FPR) and Field Service Report (FSR) submissions. etc. | 12/4/2019 |
| 13070 | ThermoFisher Scientific Gainesville, FL Associate, Quality Assurance HS diploma Exp: 1 year |
The QA Associate will participate in the day to day operations related to release functions in the Quality Assurance Department. The incumbent is responsible for the timely review and disposition of controlled materials needed to support manufacturing. These materials include, but are not limited to, sterile supplies, cell banks, viral banks, and reagents used by manufacturing or for testing processes. The associate identifies areas for improvement and ensures materials, products, and equipment within the warehouse remain in a state of control. etc. | 12/4/2019 |
| 13071 | ThermoFisher Scientific Los Angeles, CA Sales Representative BS Exp: 0+ years |
Our Sales Representative is responsible for the sales of research products and services within a defined territory, serving customers engaged in pharmaceutical, biomedical, chemical, and other fields of research and development, as well as quality assurance labs such as in food and environmental testing. The Sales Representative maintains effective customer relations, develops opportunities for growth within an existing customer base, and assures market penetration and profitability while achieving sales and profit forecasts. etc. | 12/4/2019 |
| 13072 | ThermoFisher Scientific Cincinnati, OH QC Lab Technician AS in chemistry or related Exp: 1-2 years |
Responsibilities: Testing of raw materials, finished product, and stability samples while meeting deadlines and following an assigned schedule. Accurately documenting all tests/test materials/equipment used and all results obtained. Work in accordance with approved methods, SOPs, and cGMPs/GLPs, while performing tests. Responsible for safety and to protect themselves and fellow employees from harm. | 12/4/2019 |
| 13073 | ThermoFisher Scientific High Point, NC Continuous Process Verification (CPV) Engineer BS in pharmaceutical science, chemistry, statistics, or related Exp: 1+ years |
The CPV Engineer will apply Project Management and technical expertise within the pharmaceutical industry to successfully deliver CPV program goals and outcomes while interacting with customers and meeting their expectations. CPV is a global regulatory compliance requirement which focuses on ensuring product and process stability, control, and operation within the intended design space. What will you do? Demonstrate highly effective oral and written communication skills and possess project management skills including the ability to engage the organization at multiple levels and organize CPV efforts. Work with Business Managers and the business team with Technical Transfers, new business, or other situations as related to CPV. etc. | 12/4/2019 |
| 13074 | ThermoFisher Scientific Lenexa, KS Quality Control Technologist I BS in a biological science Exp: 1-2 years |
Responsible for all quality control aspects of finished product testing. Ensure that performance of finished product is in compliance with testing standards per IFU and SOP's in addition to customer requirements and regulating agencies' guidelines. Documentation control duties per Quality assurance compliance requirements. Key Responsibilities: Review and maintain product compliance specifications, documentation control. Gain proficiency on all performance benches. Documentation of testing results and determining disposition. Maintain consistency in training in Master Control. Establish and maintain SOP criteria for inspection/testing. Responsible for maintaining department equipment and requesting consumables as needed. etc. | 12/4/2019 |
| 13075 | Lygos Berkeley, CA Analytical Chemistry Research Associate I BS in chemistry or related Exp: 0-3 years analytical experience |
Lygos is seeking an analytical chemistry research associate candidate to set up, run, clean, and maintain HPLC instruments. The successful candidate will have experience with general lab procedures, data interpretation, and reporting in a fast-paced and dynamic work environment. Execute analytical methods including: sample, standard, and mobile phase preparation, HPLC operation, HPLC calibration, data analysis, and data entry. Collaborate with the metabolic engineering team, fermentation team, and downstream processing team to ensure that results and conclusions are communicated clearly. | 12/2/2019 |
| 13076 | Lygos Berkeley, CA Software Engineer BS or higher in computer sceinces Exp: 1+ years |
The successful applicant will serve as a software engineer developing systems for that improve and automate data handling and analysis related to R&D processes at Lygos. Investigating users’ workflows and needs, creating specification documents, writing applications, and supporting both deployment and end users of applications will be necessary elements of the successful applicant’s duties. The successful applicant will be expected to advance critical aspects of Lygos’ software development efforts through both effective individual and team efforts. | 12/2/2019 |
| 13077 | LSNE Bedford, NH QC Microbiology Technician (A shift - Sun - Wed 6:00 - 4:30 pm) BS Exp: 0-1 years in cGMP environment |
Conducts sampling of incoming raw materials, product environments, and/or facility clean utilities, as per approved procedures and submits these samples to the appropriate testing facility for documented and controlled results. Applies material / system status labels, as indicative of testing status and/or results obtained. Assists with lab maintenance and inventory. | 12/2/2019 |
| 13078 | LSNE Bedford, NH QC Chemist I (Mon - Fri 1st shift) BS in analytical chemistry or related chemistry Exp: 0-3 years in analytical chemistry/QC |
This position will have responsibility for supporting all activities in the Quality Control Laboratory. This includes the testing of in-process samples, finished product and stability samples and raw materials. This may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 12/2/2019 |
| 13079 | LSNE Bedford, NH QA Associate I - Ops (Wed - Sat 3:30 pm - 2:00 am) BS in sciences Exp: 0-2 years |
This position provides QA support in the manufacturing of clinical and commercial drug products/medical devices to ensure compliance with the principles and guidelines of cGMP. QA Associates maintain the quality systems, such as laboratory control, investigation management, materials management, document control and training to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Facilities, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner. | 12/2/2019 |
| 13080 | LSNE Bedford, NH QA Associate I - Ops (Sun - Wed 6:30 am - 5:00 pm) BS in sciences Exp: 0-2 years |
This position provides QA support in the manufacturing of clinical and commercial drug products/medical devices to ensure compliance with the principles and guidelines of cGMP. QA Associates maintain the quality systems, such as laboratory control, investigation management, materials management, document control and training to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Facilities, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner. | 12/2/2019 |
| 13081 | LSNE Bedford, NH Manufacturing Technician I/III (Wed - Sat 3:30 pm - 2:00 am) HS Diploma/GED Exp: 0-2 years in GMP manufacturing, pharma/medical devices preferred |
This position is responsible for performing a variety of tasks in support of all manufacturing activities in accordance with current GMPs. Executes basic manufacturing procedures (cleaning, solution prep, equipment prep) under direct supervision. Accurately follows and completes required documentation (batch records, forms, Quality system documentation) under direct supervision. Expected to adhere to all procedures, including gowning and safety requirements, at all times. Supports manufacturing activities outside of core hours under direct supervision. | 12/2/2019 |
| 13082 | Mallinckrodt Pharmaceuticals St. Louis , MO Quality Tech II AAS/AA or BS/BA in chemistry/biology Exp: 1-3 years in cGMP |
Depending on the laboratory area, will perform analysis on Raw Materials, Intermediates, In-Process, Finished Product, or Stability samples using established analytical methods. Follow good documentation practices for the accurate and timely documentation of all activities. Perform wet chemistry testing using GMP documentation in notebooks and also ELN. Assist with establishing and maintaining safe work standards in the lab | 12/2/2019 |
| 13083 | Mallinckrodt Pharmaceuticals Hobart, NY Maintenance Tech I HS Diploma/GED Exp: 1-2 years in mechanical/electrical trades |
Performs basic preventative maintenance activities and repairs to buildings and facilities including; office areas, pharmaceutical manufacturing and processing areas, laboratories, warehouse areas, loading docks, and parking lots and driveways. May perform maintenance or simple repairs to selected types of plant equipment or systems for which mechanic has received training on. Works with various types of construction materials used for construction and finishing of walls, ceilings, and floors. Works under the supervision of the Facilities Maintenance Supervisor or, a more highly-skilled mechanic. | 12/2/2019 |
| 13084 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - A Shift 4on/4off 6am-6pm HS Diploma/GED Exp: 3-12 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. | 12/2/2019 |
| 13085 | Mallinckrodt Pharmaceuticals St. Louis , MO Quality Assurance Technician II HS Diploma, AS/AA or BS/BA preferred Exp: 1-3 years in document review in cGMP environment |
The Quality Assurance Technician II performs a variety of review processes with the intent to correct record errors in manufacturing process documentation that includes batch record review and documentation issue resolution. This role is also responsible for return good inspections, cGMP area inspections and product inspections. This role ensures QA compliance and that cGMP principles are adhered to. | 12/2/2019 |
| 13086 | Mallinckrodt Pharmaceuticals St. Louis , MO Chemical Process Engineer BS in chemical engineering Exp: 1-3 years related experience |
The Chemical Process Engineer is the recognized technical leader for chemical manufacturing processes and for the improvement of existing chemical processes. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies. Serve as main point of contact for chemical manufacturing processes in their area in regards to safety, quality, and continuous improvement activities. | 12/2/2019 |
| 13087 | Mallinckrodt Pharmaceuticals Hobart, NY Packaging Maintenance Technician - 2nd Shift HS Diploma/GED Exp: 1-2 years in mechanical/electrical trades |
Performs preventative maintenance activities on specific pharmaceutical manufacturing and/or packaging equipment and systems. Provides maintenance support to manufacturing personnel during the operation of manufacturing and packaging equipment and systems. Diagnoses problems and performs repairs on manufacturing and packaging equipment. | 12/2/2019 |
| 13088 | Mallinckrodt Pharmaceuticals Hobart, NY Project Engineer BS in engineeering Exp: 1-3 years |
Works as a key technical resource in supporting company objectives with respect to engineering design and project management in the implementation of capital projects and non-capital process improvements. Responsibilities include working with and/or leading the team to help identify, develop and execute projects to meet or exceed all company goals with respect to quality, schedule and spending. This could include: developing design concepts with the users; providing detailed design documents for some projects (e.g. P&IDs, construction drawings) ; equipment and instrument specification and installation; engineering calculations, developing request for proposals to bid projects; coordination with customers, contractors and consultants; reviewing documents, preparing capital appropriation requests, creating purchase orders, reviewing and paying invoices;; monitoring progress; assisting with training; executing commissioning activities; and ensuring proper project closure. | 12/2/2019 |
| 13089 | Mammoth Biosciences San Francisco, CA Research Associate BS/BA or MS in biology or chemistry Exp: 1-3 years in molecular biology/genetics |
Mammoth is seeking a Research Associate experienced in nucleic acid and protein biochemistry techniques to support our product development team. The ideal candidate will have experience with assay development and product commercialization related to molecular tests and reagent kits. The candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. The Research Associate will report directly to Director of Assay Development. | 12/2/2019 |
| 13090 | Masimo Irvine, CA [CLINICAL] Clinical Research Associate BS/BA in sciences Exp: 0-4 years |
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. This position must ensure that all activities will be conducted in accordance with Government Regulations (FDA, MDD and International), Good Clinical Practices (GCP) and Department Operating Procedures (DOP). Plan, implement and conclude clinical studies in support of project timelines/market release goals with minimal supervision; An advanced individual may conduct more complicated studies, as well as contribute to study proposals and protocols, applying principles of clinical study design and research methodology to assigned research projects; | 12/2/2019 |
| 13091 | Master Control Salt Lake City, UT Enterprise Support Engineer II 4-year technical degree Exp: 0-4 years |
The Enterprise Support Engineer (TSE) provides in depth, high-level technical support to MasterControl customers. The ESE II maintains systems-level expertise and root cause-level troubleshooting while resolving advanced technical issues for customers. ESE II's work with fellow team members, service consultants, sales operations and other company resources to increase customer satisfaction and loyalty. TSE's are responsible for special projects, and will maintain one or more team projects that track team analytics and team success. TSE's will be subject matter experts (SME) in one or more subjects pertaining to the support of MasterControl Customers. | 12/2/2019 |
| 13092 | Masy Bioservices Pepperell, MA Quality Associate I HS Diploma/GED Exp: 1+ year in related |
This position provides day to day support assisting in areas such as GMP, ISO 9001 and ISO 17025 compliance and the company’s quality system. Duties include quality assurance and control activities in technical, systems, operations and service areas. This position may require frequent interaction with multiple departments. Works under general supervision of management or team lead. | 12/2/2019 |
| 13093 | MDxHealth Irvine, CA Specimen Accessioner I HS Diploma, degree preferred Exp: 1-2 years |
The Specimen Accessioner I performs all paperwork and non-technical procedures required to prepare, process, and submit specimens to the laboratory for testing. Responsibilities will include but not limited to: receiving, triaging and accessioning patient samples, distribution of patient reports and specimens to clients, performing quality control of accessions and labeling. | 12/2/2019 |
| 13094 | MED Institute West Lafayette, IN Mechanical/Biomedical Engineer BS or MS in biomed/mechanical engineer Exp: 1-3 years |
This position requires a technically sound engineer capable of driving a project to completion with minimal supervision. A qualified candidate should be able to demonstrate a solid understanding of first principles, build a design from the ground up, perform independent research utilizing all available tools and resources, communicate well with customers, maintain good documentation practices, and develop and validate new test methods. Examples of commonly performed tests include accelerated fatigue, corrosion, electrosurgical, simulative use, and others that are used to evaluate material properties and/or functionality of a finished medical device. In addition, this person will be responsible for the maintenance of well-controlled documentation, including written protocols and reports, data forms, and laboratory notebooks. | 12/2/2019 |
| 13095 | Medicomp Melborne, FL Amazing Cardiac Monitoring Technician HS Diploma Exp: Certified Cardiovascular Technician |
Review data from Cardiac monitors to provide physicians with results to help determine treatment for patients. This position requires a strong ability to read and interpret EKG strips as well as communicate with Doctors, patients, and other departments throughout the organization. This is a 24/7 facility and shifts are scheduled with differential available for 2nd, 3rd and weekend shifts. | 12/2/2019 |
| 13096 | Medicomp Melborne, FL Technical Services Associate AS/AA degree Exp: 0-1 year |
We are seeking a Technical Services Associate that under minimal supervision and using average manual dexterity, performs varied skilled assembly tasks and soldering tasks necessary to produce a product by performing the following duties. In addition, this position requires basic computer skills to make transactions, transfer yield rates and data into Excel. | 12/2/2019 |
| 13097 | Medidata Metropark, NJ B2B Marketing Associate BS/BA Exp: 1-3 years in marketing/sales |
This marketer will drive direct targeted marketing for our platform and solutions by developing programs that leverage outbound marketing efforts - across online/digital and tele-prospecting tactics - to drive overall preference, satisfaction, technology adoption of our platform/portfolio and amplify market impact of our technology innovation stories. Assist and lead in the development of outbound marketing programs across a variety of product offerings, industries, segments, and personas (e.g., Clinical Ops, Data Management, Finance, IT). | 12/2/2019 |
| 13098 | Medidata New York, NY Software Engineer (C# / .Net) BS/BA Exp: 1-3 years in various coding languages |
Coder is a mature, single-instance, multi-tenant web service supporting hundreds of clinical trials. Our application is built with C#, leverages Microsoft’s SQL server database and is hosted in AWS. Our front end uses Asp.NET, HTML/CSS, Bootstrap and AngularJS. As an engineer on Coder, you'll be challenged both to develop new features in response to market demand and improve the performance and scalability of the application to meet the rapidly growing user base. | 12/2/2019 |
| 13099 | AstraZeneca Wilmington, DE Contract Operations Analyst BS/BA Exp: 0-4 years |
The Sr. Contract Operations Analyst is responsible for working with internal/external customers on all aspects of Market Access; Master Data, Contracting, Membership, Chargebacks and Rebates. They are responsible for the receipt, analysis, impact, resolution and posting/reporting of all contractual payments across multiple customer segments including Health Plans, GPOs, Specialty Pharmacies, Physicians and Wholesalers as well as maintaining all related documentation for those payments. The Sr. Contract Operations Analyst is responsible for developing Market Access contracts including: template development, strategy interpretation, language negotiation, approval, and execution In this role, they will manage and meet deliverables of business operations to monitor, evaluate and administer claims to be paid and ensure payments are accurate, timely, formulary compliant and entered in contract systems consistent with agreement terms, following corporate controls/approved guidelines and SOX regulations. | 12/2/2019 |
| 13100 | AstraZeneca Frederik, MD Quality Control Analyst BS in sciences/biotech/pharma Exp: 0-5 years |
Performs selected quality control testing activities, dependent upon assigned area, including the following: Responsible for conducting raw materials, in process, finished product and stability testing according to standard operating procedures. Completes appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms. Identifies and troubleshoots equipment problems. Enters data evaluated for compliance to specifications and reports abnormalities. Reads, understands, and follows SOP’s and complies with cGMP’s | 12/2/2019 |
| 13101 | AstraZeneca Gaithersburg, MD Research Animal Technician I BS/BA in biological sciences Exp: 0-1 years |
At AstraZeneca as the Research Animal Technician I, you will support oncology using basic technical skills such as performing daily health/mortality checks, evaluating health status of animals and performing basic technical procedures such as SC, and IP injections, cardiac blood collection, and oral gavage. Observe appropriate safety and study requirements by reading, understanding and following Standard Operating Procedures (LAR Guidelines), applicable regulations and study protocols. Observe appropriate safety and health practices including personal protective equipment and barrier requirements. | 12/2/2019 |
| 13102 | AstraZeneca Wilmington, DE Patient Safety Associate (Quality Excellence) BS/BA in biosciences, healthcare, IS/IT Exp: 1 year in pharma |
The BioPharmaceuticals Business Unit (BBU) creates and executes meaningful therapeutic area and product strategies that are focused on addressing the unmet needs of patients around the world. Conducts activities and interactions consistent with company values and in compliance with the Code of Conduct and supporting policies and standards relevant to the role. Completes all required training on AstraZeneca’s Code of Conduct and supporting policies and standards on time. Reports potential issues of non-compliance. Demonstrates a working knowledge and compliance with organizational global and local procedural documents and local implementation of objectives, policies, processes and procedures and regulatory requirements, guidelines and obligations relevant to pharmacovigilance activities and adverse event reporting, including periodic safety reporting. | 12/2/2019 |
| 13103 | AstraZeneca Frederik, MD Quality Control Technician - Laboratory Management Services (LMS) - Operations HS Diploma/GED Exp: 0-2 years work experience |
Sampling of the Utilities Systems (for example WFI, Specialty Gases, Compressed Air, Steam). Sample management activities including receipt, visual inspection for integrity, storage, distribution and disposal. Parts and glassware washing and autoclaving, including proper documentation of these activities. Detailed supervision and detailed instructions given for routine work as well as any new activities or special assignments. | 12/2/2019 |
| 13104 | Kimball Electronics Jasper, TX Manufacturing Engineer BS/BA in eletrical/mechanical engineering Exp: 0-3 years |
Leads manufacturing efforts with respect to direct customer product launches and sustaining activities. Guides, mentors and manages engineering support teams. Development of processes and DFx activities to meet customer requirements. Selection, specification and implementation of manufacturing equipment. Work directly with program management and quality engineering to ensure profitability. | 12/2/2019 |
| 13105 | Cantel Medical Pomezia, IT R&D Microbiology Associate MS in biology or related Exp: 1 year in R&D projects |
The junior microbiologist will assure to support the “in vitro” test according to EN/ISO Standards requirements. Respecting the deadlines; Check the expiration date of the reagents and the microbial strains; Fill laboratory notebooks and record the results. Ability of preparation of culture media and microbial strains suspension. They will report to local manager. | 12/2/2019 |
| 13106 | MedPace Home based, na Home-Based Clinical Research Associate - Clinical Research Coordinator Experience BS/BA in health/sciences Exp: 1 year minimum |
This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Perform qualification, initiation, monitoring, and closeout visits; Establish an open line of communication with site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Evaluate the quality and integrity of site practices – escalating quality issues as appropriate; | 12/2/2019 |
| 13107 | MedPace Cincinnati, OH Clinical Research Associate-Cincinnati Entry Level BS/BA in health/sciences Exp: 1 year work experience preferred |
Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence: PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA. | 12/2/2019 |
| 13108 | Viant Collegeville, PA Process Engineer - Metals BS/BA in material science/metallurgy or mechanical engineering Exp: 1 year |
The Process Engineer must be able to recognize, communicate, and measure technical risk for a variety of metals for use in medical, aerospace, and industrial products along with the processes and equipment used to manufacture these products. The process engineer is a central leader for addressing concerns of a technical nature. Provide diversified range of technical services to both internal and external customers supporting the attainment of company goals. Areas of support include mechanical testing, cold drawing, heat treating, nondestructive testing, and failure analysis of metal tubes | 12/2/2019 |
| 13109 | MedSpark San Luis Obispo, CA Product Development Engineer BS/BA in mechanical engineering Exp: 1 year |
You will be part of a small and nimble team that conceptualizes, develops, and proves-out designs that make an impact on the world of medicine. Your primary role is driving conceptualization, development, and prototyping of new product concepts, focused on inventive uses of new and existing technologies that open up entirely new product concepts. Work hours and days are extremely flexible, based on need and your availability. | 12/2/2019 |
| 13110 | LGC Manchester, NH Junior Staff Accountant BS/BA in accounting or finance Exp: 1-3 years in accounts |
The Junior Staff Accountant will be responsible for supporting a fast growing company at two locations (Manchester, NH & Charleston, SC) by providing transactional and reconciliatory assistance to the local Finance and Accounting team which supports both sites. The candidate will contribute across multiple key accounting areas including Fixed Assets, Accounts Receivable, and Accounts Payable. The position is located in Manchester, NH. | 11/28/2019 |
| 13111 | LGC Novato, CA EH&S Technician AS/AA or BS/BA in sciences Exp: 0-2 years |
This role is responsible for all EH&S and Material Management functions at the Novato facility. This includes but is not limited to managing raw materials coming in to the facility, movement throughout the facility, waste management, and emergency equipment inspection. Responds to all EH&S requests at the Novato facility. Organizes all hazardous waste and interfaces with hazardous waste contractor for waste disposal. Performs all safety inspections throughout the Novato facility. Documents all inspection finding and informs functional manager of pertinent findings. Acts as the Facility Operations liaison when necessary. | 11/28/2019 |
| 13112 | LGC Manchester, NH Sales Representitive BS in chemistry or life sciences Exp: 1 year in sales |
The person in this position will function primarily as a sales representative and develop and profitably grow the North American (US & Canada) revenue of the Standards business, primarily in the Food, Beverage and Cannabis sectors. The successful candidate will sell into both private and public organizations associated with Food, Beverage and Cannabis Industries and will possess ability to develop strong customer relationships. | 11/28/2019 |
| 13113 | American Regent Hilliard, OH Process Equipment Technician I - 1st Shift HS Diploma/GED Exp: Entry Level |
This entry-level position is a member of the Manufacturing Team. The Manufacturing Team is responsible for activities associated with the manufacture of safe, effective and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Manufacturing Team ensure aseptic and sanitary conditions are maintained where required, that appropriate manufacturing area and equipment records are neat and accurate and that safe, effective and professional behavior is displayed at all times. In conjunction with Production Management the Manufacturing Team provides input and assistance to other Departments as needed, playing a critical role in maintaining production schedules and meeting Company goals. The Team Member will be able to participate in all aspects of the Equipment Process. The Equipment Process includes cleaning, assembling, and sterilizing small and large pieces of equipment in accordance with established production records in a concerted effort to manufacture sterile liquid pharmaceuticals. | 11/28/2019 |
| 13114 | American Regent New Albany, OH R&D Technical Services Chemist I MS in chemical engineering/pharma chemistry Exp: 0-1 years |
Conduct the experiments under the supervision of Scientists for Tech Transfer, Process R&D/Scale up/Validation, and other activities needed for introduction of a new product into cGMP manufacturing site or to support process improvements of existing products. Execute laboratory experiments as per the protocols or under supervision to study material compatibility studies and/or cleaning validation activities. Ensure all work is performed and documented in accordance with existing company policies, procedures, current Good Manufacturing Practices, and health and safety requirements. | 11/28/2019 |
| 13115 | American Regent Shirley, NY Compounder I HS Diploma/GED Exp: Entry Level |
This entry level position is a member of the Formulation Team, who comprise a portion of the Manufacturing Team. This position will be expected to execute the required responsibilities and tasks necessary to perform as a Compounder I using current Good Manufacturing Practices (cGMP) according to approved SOPs in order to support the overall mission of the Manufacturing Team. | 11/28/2019 |
| 13116 | American Regent Shirley, NY QC Microbiologist I, EM Lab BS/BA in sciences Exp: 0-2 years in pharma lab |
The QC Microbiologist I will perform microbial testing according to current guidance and established procedures for analysis of samples in the Environmental Monitoring laboratory. Perform support work such as Quality control testing of in-house prepared and commercially purchased media, stock culture maintenance, data trending, etc. | 11/28/2019 |
| 13117 | Lumen Bioscience Seattle , WA Lab Technician BS/BA in biological sciences Exp: 1-2 years lab experience |
The full-time Lab Technician will join an essential team involved in our development of oral antibody-based therapeutics. The team member will be expected to execute leading edge molecular biology protocols, support the construction of novel cyanobacteria strains, and aid in the continued development of protocols that have made Lumen Bioscience the worldwide leader in Spirulina genetic engineering. The position requires strong organizational skills to meet quality and productivity goals. Effective communication skills are also crucial in coordinating with other members of the team, providing status updates, and raising quality or trouble shooting issues as they may arise. | 11/28/2019 |
| 13118 | Lumenis Salt Lake City, UT Test Technician AS in Laser/Electro Optics is highly desired Exp: 1-2 years in laser/optics preferred |
Responsible for performing the set-up, calibration, testing, troubleshooting of circuits, components, instruments, optical and mechanical assemblies. Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams. Tests and troubleshoots assemblies and Laser systems. May complete rework on assemblies and or systems as a result of testing. As required, prepares technical reports summarizing findings and recommending solutions to technical problems. May assist in the selection and set-up of specialized test equipment. Works on assignments that are moderately complex in nature where judgment is required in resolving problems and making recommendations. | 11/28/2019 |
| 13119 | Luuminex Austin, TX LOGISTICS COORDINATOR I - Limited Assignment -SHIPPING HS Diploma/GED Exp: 1 year in logistics/supply chain |
The Logistics Coordinator I performs a variety of shipping, stockroom, and receiving tasks. This coordinator prepares items for shipment ensuring cost effective courier services and compliance to global trade, OSHA, DOT and other regulations. Must have a high regard for compliance, attention to detail, and inventory accuracy. Responsible for material transactions within ERP System. Compares information on packing slip with purchase order to verify accuracy; Also includes reverse logistics support. | 11/28/2019 |
| 13120 | Luuminex Northbrook, IL LOGISTICS COORDINATOR I - US HS Diploma/GED Exp: 1 year in logistics/supply chain |
Performing administrative and physical duties to successfully execute shipments. This position coordinates with transportation companies, handles routine questions and problems, and communicates with other departments and customers throughout the delivery cycle to ensure a high rate of customer satisfaction. Completing documentation that is in compliance with international, hazmat, or FDA standards. | 11/28/2019 |
| 13121 | Lundbeck San Diego, CA Research Associate BS or MS biological sciences Exp: 1-3 years lab/bench experience |
The Research Associate In Vitro Screening and Biochemistry will contribute to the identification and development of novel small-molecule drugs and support Lundbeck’s CNS discovery programs. The successful candidate will work in multidisciplinary teams to discover new therapeutics, collaborating with biologists and medicinal chemists to select molecules for further in vitro characterization and to identify trends in structure-activity relationships. | 11/28/2019 |
| 13122 | United Therapeutics Corporation Silver Spring, MD Clinical Trial Administrator I BS/BA Exp: 0-1 years related experience |
The Clinical Trials Administrator I provides administrative and operational support with the set-up, execution and close-out of clinical studies as well as infrastructure development projects. Supports the department’s requirements to adhere to GCP and oversight of clinical trials. Assist the Clinical Operations team in completion of all required tasks to meet departmental and project/study goals. Develop and maintain knowledge of relevant Lung Biotechnology Inc. SOPs and Lung Biotechnology internal tracking systems. | 11/28/2019 |
| 13123 | United Therapeutics Corporation RTP, NC Research Associate I/II - Tissue Engineering, Bioprocess Development BS or MS in biological sciences/engineering Exp: BS: 1-3 years, MS: 0-2 years |
Evaluate the function of native and engineered lung tissues and assist with implementation of new analytical regimes to characterize the function of the engineered lung tissues. Assist with data collection and analysis in support of these objectives. Contribute to preparation of human and non-human organs and tissues for experimentation. Prepare specific supplies and materials for designated testing, including design and construction of tubing circuits, preparation of perfusate, and maintenance of equipment used for functional assessment experiments. | 11/28/2019 |
| 13124 | United Therapeutics Corporation RTP, NC Bioprocess Technician - Cell Biology AAS/BA/BS in biological sciences Exp: 1+ year in industry/lab |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. Routinely perform large-scale primary lung cell culture in 2D and 3D to support process development activities for a tissue engineered product. Routinely perform bioanalytical assays to phenotypically and functionally characterize cells (such as flow cytometry and plate-based assays). Generate data for process development studies to improve yield, purity, and quality of primary lung cell types | 11/28/2019 |
| 13125 | Starkey Hearing Technologies Eden Prairie, MN Software Tester I BS/BA Exp: 1-2 years |
Software Tester: Conduct Software Testing on software applications. Perform system level testing on Starkey’s Software and Hardware systems working either in a team or independently. Follow standard Configuration Management practices and utilize a defect tracking tool. Tracking quality assurance metrics such as defect densities and open defect counts. Resolve and provide solutions to internal and external customer related issues. Participate in the development and implementation of structured testing concepts, methodologies and automated testing tools where applicable. etc. | 11/26/2019 |
| 13126 | Starkey Hearing Technologies Eden Prairie, MN Mechanical Designer I - F&T AS/AA Exp: Not necessary for Associate candidates |
This position is responsible for designing new assembly tooling and assembly fixtures for product assembly. The position also requires designing tooling and solutions for specific tests and departments as requested. All tools/solutions must meet quality and manufacturing specifications provided by standards and the customer. Approach and Deployment: Design tools for production and specialty use. Utilize CREO to create accurate component, assembly and system models and drawings. Ensure designs meet performance, manufacturing, quality, cost and design requirements. Coordinate and lead design reviews as required. etc. | 11/26/2019 |
| 13127 | Starkey Hearing Technologies Eden Prairie, MN Financial Analyst BS/BA in accounting, finance, or economics Exp: 1-2 years |
Starkey Hearing Technologies, a well-respected, mission focused and high-impact organization, is currently seeking a Financial Analyst. This position is responsible for analyzing and communicating the financial performance for assigned product lines and cost centers. The Financial Analyst will identify and implement lean work-processes and key reporting measurements. The Financial Analyst is responsible for the preparation and completion of annual operation and capital budgets – for assigned cost centers and product lines. etc. | 11/26/2019 |
| 13128 | SDC Tempe, AZ Biostatistician MS in biostatistics, statistics, or related Exp: 1-3 years |
Supports lead biostatistician on clinical studies; may serve as lead biostatistician with oversight from a more senior biostatistician. Maintains the statistical integrity of clinical trials analyzed by SDC. Assists in preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, and writing statistical sections of clinical study reports. etc. | 11/26/2019 |
| 13129 | Stealth Biotherapeutics Newton, MA Supply Chain Associate BS Exp: 1 year |
This position will report to our Director, Clinical & Commercial Supply Chain. This role is responsible for supporting continuous material supply in support of clinical and commercial demands. The individual will work with internal/external customers and suppliers in order to assist in developing processes for shipment of material and inventory reporting. Responsible for monitoring inventory levels and providing feedback regarding expiry and resupply. etc. | 11/26/2019 |
| 13130 | Stellartech Milpitas, CA Quality Engineer I/II BS Exp: 0-2 years |
Stellartech is looking for a Quality Engineer to join our Team. Responsibilities: Perform quality engineering development activities for new product designs by assisting Engineering in the preparation of design and development plans, Design History File documentation, and Design History File preparation. Review and approve Device Master Record documentation for new product design and maintenance, including: bills of material, assembly procedures, manufacturing operations, assembly diagrams, test procedures, component specifications, labeling, and operator’s manuals. etc. | 11/26/2019 |
| 13131 | Stellartech Milpitas, CA Electrical Engineer BS in hardware or electrical engineering Exp: 0-2 years |
Stellartech is looking for a Electrical Engineer to join our Team. Responsibilities: Design, develop, and document electronic hardware for medical devices. Specify procedures and fixtures to test electronic medical devices. Assist manufacturing in prototype and pilot builds of electronic medical devices. Assist manufacturing in hardware problem analysis and solutions. Assist in training of technicians and manufacturing staff on new products and procedures. etc. | 11/26/2019 |
| 13132 | Stereotaxis Saint Louis, MO Field Service Engineer AS/AA in electronics or equivalent Exp: 1-5 years |
Provide on site and remote service and support of Stereotaxis magnetic navigation systems including permanent magnets, and servo control systems. Interface with customers and vendors to ensure a quality service experience and that all expectations are met. ESSENTIAL JOB RESPONSIBILITIES: Interface with customers to obtain accurate details of the equipment service needs and provide updates regarding the progress of the service/installation. Diagnose and repair control servo control systems. etc. | 11/26/2019 |
| 13133 | Stereotaxis New York City, NY Clinical Specialist BS in biomedical engineering, life sciences or related Exp: 1-3 years |
The Clinical Specialist (CS) provides customers and end users with product, clinical/ technical, educational, and sales support to maximize recurring revenue, utilization of company products, and customer service objectives. Must meet customer expectations by striving without reserve for the greatest possible reliability and quality in our products, processes, and systems by being accountable, having a voice, and taking action. Clinical Specialist will spend a high percentage of their time in procedures which requires a person to develop clinical knowledge within electrophysiology (EP), develop in-depth expertise of the Niobe remote navigation system, along with displaying outstanding sales abilities and the assertiveness needed to drive the Stereotaxis business. etc. | 11/26/2019 |
| 13134 | Steripharma Syracuse, NY Production, Clean Room Pharmaceutical Technician - 3rd Shift AS/BS Exp: 1+ year(s) |
This position operates production equipment, to include non-sterile filling machines, and packaging and labeling machines. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. etc. | 11/26/2019 |
| 13135 | Steripharma Syracuse, NY Production Maintenance Technician, 2nd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. How you make a difference . . . you will . . . Performs maintenance work, to include equipment repair and preventative maintenance work as required or assigned. Performs the repair and maintenance of APA area floors and walls. Completes work orders and projects as assigned, supporting each team member as directed. etc. | 11/26/2019 |
| 13136 | Steripharma Syracuse, NY Production, Clean Room Pharmaceutical Technician - 2nd Shift AS/BS Exp: 1+ year(s) |
This position operates production equipment, to include non-sterile filling machines, and packaging and labeling machines. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. etc. | 11/26/2019 |
| 13137 | Steripharma Syracuse, NY Production, Pharmaceutical Production - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
This position operates vial wash/packaging production equipment. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. etc. | 11/26/2019 |
| 13138 | Steripharma Syracuse, NY Production Maintenance Technician, 3rd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. How you make a difference . . . you will . . . Performs maintenance work, to include equipment repair and preventative maintenance work as required or assigned. Performs the repair and maintenance of APA area floors and walls. Completes work orders and projects as assigned, supporting each team member as directed. etc. | 11/26/2019 |
| 13139 | Steris Scranton, PA Installation Technician AS/AA in electronics, mechanical, or similar Exp: 1+ year(s) |
STERIS’ Installation Technicians act as the face of STERIS by achieving One of a Kind Service for our Customers. The Installation Technician is a field-based, Customer-facing role that primarily travels to Customer sites (medical facilities) to install Operating Room and Sterile Processing Department equipment. They provide complete equipment installation in accordance with plans and specifications including scheduling, delivery, installation, check-out, and final inspection of equipment. Installation Technicians are also responsible for building positive relationships with Customers and peers, as well as completing necessary administrative tasks. | 11/26/2019 |
| 13140 | Steris Sacramento, CA Field Service Representative I AS/BS in electronics, mechanical, or similar Exp: 1-2 years |
Position acts as Trusted Advisor to STERIS Customers in maintenance and procurement of medical devices and consumable products as part of a high performing team. Drive an exceptional Customer experience by providing on-site preventative maintenance, troubleshooting, repair, equipment modification and installation support on complex mechanical, electro-mechanical and electronic units in a high stress healthcare environment. Provide superior Customer service by pro-actively interacting and communicating with Customers. Utilize advanced technology to complete administrative requirements, aid in troubleshooting issues and improve the overall Customer experience. Promote STERIS growth through identifying and recommending products and services to Customers. etc. | 11/26/2019 |
| 13141 | Steris Martinez, CA Field Service Representative I AS/BS in electronics, mechanical, or similar Exp: 1-2 years |
Position acts as Trusted Advisor to STERIS Customers in maintenance and procurement of medical devices and consumable products as part of a high performing team. Drive an exceptional Customer experience by providing on-site preventative maintenance, troubleshooting, repair, equipment modification and installation support on complex mechanical, electro-mechanical and electronic units in a high stress healthcare environment. Provide superior Customer service by pro-actively interacting and communicating with Customers. Utilize advanced technology to complete administrative requirements, aid in troubleshooting issues and improve the overall Customer experience. Promote STERIS growth through identifying and recommending products and services to Customers. etc. | 11/26/2019 |
| 13142 | Steris Chicago, IL Sterile Processing Technician HS diploma or equivalent Exp: 1+ year(s) |
Provides on-site support for the reprocessing of surgical instruments and trays to contracted facilities in compliance with the Department of Health, TJC, OSHA, CDC, AAMI and AORN standards and facilities goals and policies. Position level will be determined by previous job related experience, performance and certification requirements. Duties: Operates all mechanical machinery; cart washers, instrument washers, steam sterilizers, low temp sterilizers, ultrasonic and drying cabinets, within sterile processing. Uses established policies and procedures to complete work assignments. Learns and trains in all areas of sterile processing including decontamination, cleaning, assembly, wrapping, sterilization, and storage processes within all set professional standards and regulations. etc. | 11/26/2019 |
| 13143 | Steris Birmingham, AL Customer Care Representative I BS/BA Exp: 0-2 years |
The primary focus of this position is to provide an outstanding Customer experience. Individuals in this role will be assigned to a manageable level of sales representatives and will serve as a liaison between the sales representative and the Customer. In this role, the Customer Care Specialist must have a thorough knowledge of all the Company’s products and services. Duties: Creates a personalized relationship with each assigned Account Mangers. Owns the service support experience for assigned Sales Representatives. Must be knowledgeable on where to send what repairs including responding to inquiries about IMS capabilities. Creates critical paperwork for the Customer and develops knowledge on how to make corrections, split orders and work multiple orders. etc. | 11/26/2019 |
| 13144 | Steris Denver, CO Integration Technician AS/AA Exp: 1 year |
Install operating room integration equipment as directed by Integration Specialist (I and/or II) and/or Integration Project Manager. Perform preventative maintenance, troubleshooting, repair, equipment modifications, and installation on all integration equipment serviced by STERIS. Help drive STERIS initiatives for growth and development of business. Interact with customers in a professional and knowledgeable basis. Complete administrative requirements as required. Duties: Help install operating room integration systems. This includes physical placement of equipment, installation, termination and interconnection of all cables, downloading and configuration of software; and testing of all functions per test documentation as required. etc. | 11/26/2019 |
| 13145 | Steris Bellevue, WA Field Service Technician AS/AA in electronics, mechanical, or similar Exp: 1 year |
The Field Service Technician provides preventive maintenance, troubleshooting, repair, calibration and installation support on various mechanical, electro-mechanical, and electronic units. The Technician Interacts with customers on a daily basis and completes associated administrative tasks as required. Think of this as an electrical-mechanical-plumber-Customer Service Technician all rolled into one! Every day, something special happens at STERIS. What will YOU help us do next? Duties: Perform preventive and corrective maintenance required on STERIS and related product lines. This includes: disassembling, replacing, or repairing defective parts; reassembling as required; troubleshooting, adjusting/calibrating ready for use by using standard and specialized tools by using technical manuals etc. etc. | 11/26/2019 |
| 13146 | Surgical Specialties Tampa/Orlando, FL Sales Representative, Ophthalmic BS/BA in business or a medical field Exp: 1-3 years |
Caliber Ophthalmics is currently seeking a Surgical Sales Representative to be based in Florida. As a valued employee at Caliber, you will enjoy a total benefits package including competitive salary, medical/dental/vision/life insurance, short-and long-termdisability, 401k, and more. The Surgical Sales Representative is responsible for managing the Floridasales territory, working directly with surgeons for the sale and promotion of our Caliber Ophthalmic portfolio of surgical device products to include our disposable knives, suture, and other microsurgical products. Target call points are hospitals and ambulatory surgery centers. In this surgical sales role, you will be responsible for maintaining and growing annual sales volume in Florida. | 11/26/2019 |
| 13147 | Strand Therapeutics Cambridge, MA Associate Scientist I, Molecular Biology BS/MS Exp: 1-3 years |
We are looking for a highly motivated and innovative candidate for the role of Associate Scientist I, Molecular Biology.This is a fantastic opportunity to make a significant impact as a scientifically motivated self-starter capable of independently conceiving, conducting, and critically analyzing his/her own work with minimal supervision. You are someone who is: Passionate about science and takes a proactive approach to learning new technologies and methodologies. Undeterred by difficult problems and enjoys solving them as a team, though you are comfortable contributing on anindependent level when necessary. etc. | 11/26/2019 |
| 13148 | Iovance San Carlos, CA Contract Drug Safety Associate Healthcare professional degree w/BS or AA Exp: 0-2 years |
The Drug Safety Associate candidate works in a team-oriented, dynamic, and collaborative environment. This person would manage the drug safety mailbox, track case workflow, support the drug safety team, review serious/adverse event information, and review case narratives. | 11/24/2019 |
| 13149 | Iqvia Atlanta, GA Vaccine Sales Representative BS/BA Exp: 1 year in healthcare/sciences |
Vaccine Sales RepresentativeThe Vaccine Sales Representative will be responsible for achieving stated business goals of product sales within assigned portfolio and geography through strategic territory and account management and building solid working relationships. Responsible for providing healthcare providers with all relevant information that promotes quality healthcare decisions. Maintains an expert product knowledge base including patient education, consumer education, and factors influencing the market environment. Understands and uses approved promotional materials to support marketing message. | 11/24/2019 |
| 13150 | Iqvia San Juan Capistrano, CA Vaccine Study Specialist BS/BA in sciences Exp: 1 year in GCLP lab |
Provides internal oversight and conducts the day to day running of a project throughout its life at Q2 Solutions, including method development, method validation, and sample analysis while adhering to timelines, SOPs and performance metric standards. Serves as internal liaison between the production lab scientists and project management team. Provides daily direction and feedback to laboratory staff regarding Vaccines studies. Effectively and efficiently coordinates and communicates with relevant internal support groups as needed for the study. | 11/24/2019 |
| 13151 | Iqvia New Brunwick, NJ QA Engineer 1 BS/BA in related field Exp: 1-2 years in software testing |
Work closely with Development, Functional/Business and QA teams in all the phases of SDLC. Review the requirements and provide the QA estimations and raise any concerns or issues as needed . Involved right from the requirements grooming and will prepare the logical test scenarios & test cases as needed. Prepare test scenarios & test cases and requirements traceability matrix (RTM) to ensure the complete coverage | 11/24/2019 |
| 13152 | Ironwood Albany, NY Clinical Sales Specialist BS/BA Exp: 1 year in pharma sales |
Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients. Representative must demonstrate a strong understanding of relevant disease states and possess a solid ability to communicate necessary technical, scientific, and product and disease management information to customers. Drive sales performance in a compliant manner and work to meet or exceed territory sales goals through execution of regional and national marketing strategies | 11/24/2019 |
| 13153 | Ironwood Tyler, TX Clinical Sales Specialist BS/BA Exp: 1 year in pharma sales |
Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients. Representative must demonstrate a strong understanding of relevant disease states and possess a solid ability to communicate necessary technical, scientific, and product and disease management information to customers. Drive sales performance in a compliant manner and work to meet or exceed territory sales goals through execution of regional and national marketing strategies | 11/24/2019 |
| 13154 | FujiFilm Santa Ana, CA Powder Formulation Tech HS Diploma/GED Exp: 1-2 years hands on experience |
We are hiring for a Powder Formulation Tech. The Powder Formulation Tech is responsible for the formulation of our company’s powder cell culture media products. NOTE: The current opening is on our second shift (1:00 PM – 9:30 PM). Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. Uses Mettler-Toledo IND780 terminal system to ensure correct raw materials assigned in the batch record are used and at the specified quantity. Reviews lot folders for accuracy, completeness and availability of components necessary to complete job prior to the scheduled date of production | 11/24/2019 |
| 13155 | Genetech San Francisco, CA QC Analyst BS/BA in sciences Exp: 0-5 years |
The Senior QC Analyst will perform analytical, biochemical, and/or biological testing; data review; and/or related activities that support QC operations. Perform a broad variety of basic and moderately complex tests with documentation according to GMP. Maintain accountability for deliverables affecting department and organizational objectives. Accountable for exhibiting behaviors as described by Genentech/Roche Core Competencies. | 11/24/2019 |
| 13156 | Jubilant Spokane, WA Technician IV, Environmental Monitoring HS Diploma/GED Exp: 1 year in pharma/lab |
The Environmental Monitoring (EM) Technician IV is required to perform the basic functions associated with environmental monitoring. Incumbents are required to learn the laboratory functions, sanitization procedures, and donning scrubs for ISO 8 sampling requirements. Sampling, initiating tests and collecting test results related to defined quality parameters for surface, air, product and utility systems such as compressed gases and WFI. | 11/24/2019 |
| 13157 | Just-Evotec Biologics Seattle, WA Associate Scientist, Drug Product BS in Chemistry, Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering or related Exp: 0-3 years |
Support scientific staff with various protein characterization methods including SE-HPLC, sub-visible particle analysis (HIAC and Flowcam), protein concentration (UV-Vis), pH, osmo, buffer exchange and viscosity. Execution of established high throughput biophysical methods. Perform lab maintenance tasks will include buffer preparation, tracking/ordering consumables, and shipping/receiving samples. | 11/24/2019 |
| 13158 | Just-Evotec Biologics Seattle, WA Associate Scientist, Process Development BS in Chemistry, Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering or related Exp: 0-3 years |
The successful candidates will have some experience in one or more of the following areas including chromatography, filtration, electrophoresis, analytical chemistry, cell culture and/or bioreactor operations. Experience with high throughput, robotic techniques for analytical testing, chromatography, and/or protein expression, as well as statistical design of experiments and/or process modeling, is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. This position may include the opportunity to rotate through different functional areas to gain experience in different techniques and disciplines. | 11/24/2019 |
| 13159 | Just-Evotec Biologics Seattle, WA Process Engineer I/II – Purification BS in biological sciences/engineering Exp: 1-3 years |
This team member will be responsible for the manufacture of mammalian cell-based biotherapeutics for clinical use under cGMP conditions. Under direct/moderate supervision, job responsibilities include set-up, operation, and maintenance of disposable-based manufacturing equipment; execution of manufacturing process operations; and assist in general lab operations. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures, and manufacturing documentation. | 11/24/2019 |
| 13160 | Navitas Rockville, MD Research Assistant - KAI Research BS/BA Exp: Entry Level |
Assist in the development of client deliverables according to project requirements, including but not limited to, project-specific documentation, operating procedures, and work flows with direction of more experienced staff. Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensure appropriate distribution of materials to internal and external research personnel and sites. Prepare general correspondence, agendas and meeting minutes, reports, and other project-specific documentation. Ensure review, approval, and distribution to internal staff and external project participants. | 11/24/2019 |
| 13161 | KBI Biopharma Durham, NC Research Associate I-Analytical Development (6 month temp to hire) BS Exp: 0-2 years |
Perform contract development services, including analytical development programs for monoclonal antibodies, recombinant proteins and peptides. Capable of performing bio-analytical techniques such as HPLC/UPLC, IEF, CE, Plate-based assays (ELISA, etc), qPCR, SDS- PAGE, Western Blot, with minimum training and under supervision. Prior hands-on experience or knowledge with chromatography, CE, IEF and plate-based assay is a plus. | 11/24/2019 |
| 13162 | KBI Biopharma Durham, NC Manufacturing Associate I-Upstream (temp to hire) BS/BA or AA Exp: 0-1 years |
Responsible for a wide variety of cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Follow SOPs, perform daily tasks in a clean-room, retain records and write reports. May also be responsible for troubleshooting. Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP’s and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation. Follow specific techniques and operations while demonstrating an understanding of cGMPs and how they apply to specific responsibilities. | 11/24/2019 |
| 13163 | KBI Biopharma Durham, NC Quality Systems Software Architect I/II BS/BA in pharma/biological sciences/ or chemistry Exp: 1-2 years in quality or validation |
Responsible for quality computer system administration, providing technical/end user support for quality computer system, and maintaining close communication with management to keep stakeholders apprised of quality computer system incidents/ resolutions, project validation status, and other relevant issues. The role requires leading and/or assisting in quality computer system validation efforts and ensuring all work is carried out in compliance with cGMPs, company policies and procedures, 21 CFR Part 11, EU Annex 11, ICH guidelines, and other applicable industry regulations. | 11/24/2019 |
| 13164 | KBI Biopharma Boulder, CO Engineer I/II - Manufacturing Science and Technology BS/BA or MS in sciences or engineering Exp: BS/BA: 1-5 years, MS: 0-3 years |
The successful candidate will apply scientific and engineering principles to support new biopharmaceutical process enrollments into the cGMP manufacturing facility. The candidate will: Perform all aspects of facility fit activities to support program enrollment including generating process flow diagrams, bill of materials (BOM), new specifications, and Äkta chromatography methods. Collaborate with process development and manufacturing teams to perform technical transfer and facility fit activities for downstream processes. | 11/24/2019 |
| 13165 | KBI Biopharma Durham, NC Research Associate/Sr. Research Associate BS or MS in chemistry/biochemistry Exp: 0 years |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. | 11/24/2019 |
| 13166 | KBI Biopharma Boulder, CO Manufacturing Associate I/II HS/GED, or BS/BA Exp: HS: 0-3 years, BS: 0 years |
This position is for a 2-week cycle, day shift with every other weekend off. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality.Assist in execution of procedures for microbial manufacturing, purification, or support area of manufacturing using SOP's and batch record. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. | 11/24/2019 |
| 13167 | KBI Biopharma Boulder, CO Microbiology Environmental Services Associate BS in sciences Exp: 0 years |
Performs microbiological in-process and release testing in support of GMP manufacturing. Tests include, but are not limited to, bioburden, microbial purity and endotoxin. Execute environmental monitoring within all classified manufacturing areas according to approved SOP’s and cGMP’s. Review EM data for completeness and accurate, and assist with data trending. Provide EM support for manufacturing during specified dynamic conditions. | 11/24/2019 |
| 13168 | Keystone Nano State College, PA Research Chemist MS in biological sciences/chemistry/engineering Exp: 0-2 years lab experience |
Keystone Nano is looking for a Research Chemist able to play an important role in developing novel drug products for cancer applications. The successful candidate will join our laboratory in State College, PA to conduct chemical and physical experiments using our proprietary manufacturing techniques to develop and scale this technology for a variety of markets. Set up and conduct chemical experiments, tests, and analyses using techniques such as spectroscopy, chromatography, physical and chemical extractions, dynamic and quasi-electric light scattering and microscopy, Compile and interpret results of tests and analyses Prepare graphs and charts to document experimental results for presentation to management. | 11/24/2019 |
| 13169 | KSQ Therapeutics Cambridge, MA Associate Scientist, ImmunoBiology Target Discovery/Validation BS or MS in biology/immunology Exp: 1-2 years research experience |
KSQ Therapeutics, Inc. is seeking an exceptional and highly motivated Associate Scientist, Target Discovery/Validation in the Immunobiology group to apply their experience in immunology towards the development of the next generation of impactful immunotherapies. This person will contribute to both target discovery and target validation efforts as well as in supporting our pre-clinical Immuno-Oncology small and large molecule portfolio. | 11/24/2019 |
| 13170 | KVK Tech Newtown, PA Microbiologist MS in biological sciences Exp: 0-5 years |
Validate Bacterial Endotoxin test method and test of finished products with gel clot and kinetic method; Perform and validate anti-microbial effectiveness Testing; Perform Sterility testing and validation using Steritest equinox System for finished products, Aseptic process stimulation; Identify genus level microorganisms using Vitek-2 ID; Perform Environmental Monitoring in aseptic and other controlled areas in ISO-5/6/7/8; Recover Bio burden by Various Microbial enumeration methods; Endotoxin recovery studies, Qualification of Microbiological equipments like Steritest Equniox | 11/24/2019 |
| 13171 | KVK Tech Newtown, PA Topical Formulation Associate MS in bio/chemistry/pharma sciences Exp: 1-3 years |
Person exhibits aptitude in assisting in the development of topical product pharmaceutical formulations, as well as meeting timelines for the department. Assist in the development of broad range of topical product pharmaceutical formulations including gels, creams, solutions and ointments. Develop pharmaceutical formulations utilizing Quality by Design (QbD) and risk assessment concepts. Contribute and support the analytical efforts and interpretation of data generated from experimental batches. | 11/24/2019 |
| 13172 | KVK Tech Newtown, PA Quality Control Microbiologist BS in microbiology Exp: 0-1 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensure their delivery in an accurate and timely manner following proper safety precautions. Also provide QC microbiology support to the Aseptic Manufacturing and validation process. | 11/24/2019 |
| 13173 | LabCorp Lakewood, CO Specialty Lab Assistant HS Diploma/GED Exp: 1-2 years |
This position will work both in the processing of cytology samples for testing, as well as working in the accessioning department to receive samples. Processing of samples by loading them into instrumentation to make slides. Handling/Processing/Centrifugation of laboratory specimens, primarily blood and urine specimens. Running image guided slides through imager to prepare for testing | 11/24/2019 |
| 13174 | LabCorp Houston, TX Medical Technologist/Medical Technician AA/AS or BS/BA in med lab technology Exp: 1-3 years |
Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. * Monitor, operate and troubleshoot instrumentation (can include specific dept instrumentation) * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Able to resolve technical, computer, and customer service problems within the specified department. * Deliver quality patient care while maintaining efficiency. * Perform preventive maintenance and quality control with appropriate documentation and communication. * Assist in processing of specimens when needed. | 11/24/2019 |
| 13175 | LabCorp Humble, TX Medical Technologist/Medical Technician AA/AS or BS/BA in med lab technology Exp: 1-3 years |
Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. * Monitor, operate and troubleshoot instrumentation (can include specific dept instrumentation) * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Able to resolve technical, computer, and customer service problems within the specified department. * Deliver quality patient care while maintaining efficiency. * Perform preventive maintenance and quality control with appropriate documentation and communication. * Assist in processing of specimens when needed. | 11/24/2019 |
| 13176 | LabCorp South Bend, IN Lab Assistant HS Diploma/GED Exp: 1-2 years |
The position will receive samples and prepare them for analysis via plating, centrifugation, gram stain preparation and maintenance of instrumentation.This position will include repetitive motion and extended time on feet, and also includes handling of biological samples (Urine, stool, bacterial swabs, sputum, body fluids). Prior experience handling samples preferred. | 11/24/2019 |
| 13177 | Lake Pharma Worcester, MA Associate Scientist I, Cell Culture BS Exp: 0-5 years |
The successful candidate will be able to execute hands-on laboratory work in cell culture including planning and executing shake flask, bench scale bioreactor, bench scale purifications and large-scale bioreactor experiments. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. | 11/24/2019 |
| 13178 | Lake Pharma Worcester, MA Associate Scientist I, Molecular Biology AS or BS in biology Exp: 0-3 years |
The employee will be responsible for executing projects within the laboratory, writing study/research plans, and summarizing data to clients and colleagues via technical reports. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. | 11/24/2019 |
| 13179 | LifeMine Cambridge, MA RA, Microbiology BS or BA in biology Exp: 1 year of lab experience |
We are seeking a Research Associate level candidate to support media production and to handle and clean glassware and perform the appropriate cleaning services required for each piece of glassware. This individual will perform machine washing, handwashing, dry sterilizing, autoclaving, plugging and oven and air-drying of glassware. Plus prepare diverse media to support the discovery and scale-up fermentation teams. The incumbent will be enthusiastic about working in an exciting start up. | 11/24/2019 |
| 13180 | LifeSensors Malvern, PA Entry Level Scientist BS or MS in biological sciences or related Exp: 0-2 years lab experience |
We are seeking individuals who arepassionate about research, bringout of the box thinking and take bold steps todevelopinnovativetechnologies with applications in the ubiquitin research field.Successful candidates will have basic knowledge of biochemistry and molecular biology techniques, in particular experience with, protein expression andpurification and cloning. Knowledge of the ubiquitin proteasome pathwayis desired. | 11/24/2019 |
| 13181 | Lipocine Salt Lake City, UT Associate Scientist BS or MS in life sciences, chemical engineering or related Exp: 1-3 years in pharma/chemical lab |
Associate scientist needed in the area of pharmaceutical drug delivery research. Responsibilities include conducting laboratory experiments in support of formulation and process development. Qualified candidates will possess a BS/MS in life Science, chemical engineering or related field or 1-3 years experience in a pharmaceutical or chemistry laboratory. Knowledge of laboratory practices and demonstrated skills in analytical instrumental techniques (e.g. HPLC) are preferred. Excellent communication skills needed for preparing and following standard test methods and reporting experimental results. | 11/24/2019 |
| 13182 | LoXo Oncology South San Francisco, CA Clinical Research Asscoiate BS in relevant Exp: 1-3 years in clinical trials |
The Clinical Research Associate in collaboration with the Clinical Trial Manager, contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities’ regulations/guidelines, and applicable SOPs/WPs. Responsibilities may include participation on one or more cross-functional study team(s) and/or performance and quality oversight of one or more Contract Research Organization (CRO) teams and vendors. | 11/24/2019 |
| 13183 | LabCorp South Bend, IN Lab Assistant (Auto Lab) HS Diploma/GED Exp: 1-2 years |
We are looking for a Lab Assistant within our Automated Lab department at the laboratory located in South Bend. The position will receive samples and prepare them for analysis via plating, centrifugation, gram stain preparation and maintenance of instrumentation. This position will include repetitive motion and extended time on feet, and also includes handling of biological samples (Urine, stool, bacterial swabs, sputum, body fluids). | 11/24/2019 |
| 13184 | LabCorp South Bend, IN Lab Assistant - Microbiology HS Diploma/GED Exp: 1-2 years |
This position will include repetitive motion and extended time on feet, and also includes handling of biological samples (Urine, stool, bacterial swabs, sputum, body fluids). | 11/24/2019 |
| 13185 | LabCorp Washington DC, Do Phlebotomist HS Diploma/GED Exp: 1-2 years |
Perform blood collections by venipuncture and capillary techniques for all age groups. Collect specimens for drug screens, paternity tests, alcohol tests etc. Perform data entry of patient information in an accurate and timely manner. Process billing information and collect payments when required. Prepare all collected specimens for testing and analysis. Maintain patient and specimen information logs | 11/24/2019 |
| 13186 | LifeCore Chaska, MN Cleanroom Technician HS Diploma/GED Exp: 1-3 years |
This individual will be responsible for operating all formulation/filtration equipment in a class 100 cleanroom. They will follow the process flow and communicate any processing variations to the supervisor; understand and adhere to assigned standard operating procedures; demonstrate proficiency through the routine performance of procedures; test and prepare various process filters; clean and sterilize process tanks, filters, and equipment; accurately measure out product components and record in batch record; formulate and filter product according to prescribed procedures; utilize aseptic technique and record all steps as they occur utilizing Good Documentation Practices. | 11/24/2019 |
| 13187 | LifeCore Chaska, MN Associate QC BS in microbiology Exp: 0-2 years lab experience |
This individual will ensure accurate, reproducible, and timely QC testing in support of manufacturing; support development, validation and stability studies on an as-needed basis; participate in methods improvements within the laboratory. They will perform testing on in-process product, final product, and raw materials for routine testing, validation testing, and stability testing; communicate results through appropriate documentation and batch records, statistical analysis and trending; acquire and maintain cleanroom and gowning qualification; participate in rotation to provide weekend and holiday coverage; perform instrument maintenance; identify and report equipment and method failures; identify areas for continuous improvement. | 11/24/2019 |
| 13188 | Genetech Vacaville, CA Manufacturing Technician - BioProcess BS/BA in Biological Sciences, Physical Sciences, or Engineering Exp: 0-2 years |
Provide support to Manufacturing to meet production demands. Duties include but are not limited to: CIP/SIP of portable and Freeze/Thaw tanks; clean, assemble, and autoclave 20L fermenters; prepare and autoclave manufacturing assemblies; autoclave solutions; clean and Kanban, glassware, parts and equipment; perform weighing and kitting of components; handle and aliquot hazardous materials; Provide quality materials and service to our customers. | 11/24/2019 |
| 13189 | Invenra Madison, WI Research Associate - Antibody Display BS in biological sciences Exp: 1 or more year in research |
This individual will support the development of the Invenra antibody discovery platform. Aspects of the job entail cloning, antibody library panning and protein target preparation. The successful candidate will work with other scientists within the team and will become proficient in antibody display technologies. The position requires excellent scientific and problem-solving skills, with a strong focus on creative solutions to technical problems. | 11/20/2019 |
| 13190 | Invenra Madison, WI Laboratory Support Technician HS Diploma/GED and enrolled in college Exp: 0 years |
Invenra is seeking a highly motivated laboratory support technician. This individual will maintain the laboratory and laboratory supplies in a clean, ready and working order. The position will work collaboratively with others to implement process improvements that increase efficiency and quality in the laboratory. This is a part-time position. | 11/20/2019 |
| 13191 | Invicro Boston, MA Associate Scientist, Chemistry MS Exp: 1-3 years in academic/pharma labs |
We seek individual who is an accomplished scientist with some experience in radiochemistry of small and large molecule imaging tracers for preclinical nuclear medicine imaging studies, including both PET and SPECT. Though the radiochemistry experience is not mandatory, the ideal candidate needs to have experience in organic synthesis and analytical chemistry. The candidate should have strong desire to learn radiochemistry and be able to operate and troubleshoot automated synthesis systems and analytical equipment. Most of the radiochemistry training will be provided but hands-on experience with handling radioactive materials, labeling with radioactive isotopes, purification, and formulation for in vivo imaging and biodistribution studies will be an advantage. | 11/20/2019 |
| 13192 | Invicro Boston, MA Histology Technician BS or histotech certification Exp: 0-2 years in histology/autoradiography |
The Histology Technician works in the laboratory to perform and support ex vivo studies including, but not limited to, histology, autoradiography, 3D fluorescence imaging, and cell culture. The ideal candidate will have hands-on experience in a pharmaceutical histology laboratory performing standard histology studies – embedding, sectioning and chromagen/fluorescent antibody staining. In addition, the ideal candidate will have a proven track record and competence in histology or autoradiography method development. The individual in this role will be expected to understand and carry out analysis to inform his/her own development efforts and assist in-house analysts. | 11/20/2019 |
| 13193 | Invitae San Francisco, CA Lab Accessioning BS in sciences/clinical lab studies Exp: 0-2 years |
Our Laboratory Accessioning Associates are responsible for preparing laboratory specimens prior to laboratory analysis and testing. This individual should have excellent attention to detail, effective communication skills and the ability to work independently and in a team environment. This role requires being on-site at our SF office location, with either a Monday - Friday or Tuesday - Saturday schedule. | 11/20/2019 |
| 13194 | Thermo Fisher Scientific Fair Lawn, NJ Distillation Tech. - Liquids HS Diploma/GED or AA/AS Exp: 1-2 years in admin |
The Distillation technician supports the Operations Manager and Production Supervisor in achieving daily production targets prioritized by Safety, Quality, Delivery and Cost. Following the priorities set by the Manager and Supervisor ensures that distillation columns are operating safely per procedures and to meet daily production goals laid out by supply chain. | 11/20/2019 |
| 13195 | Thermo Fisher Scientific Cambridge, MA Lab Technician BS in life sciences Exp: 1-3 years industry experience |
The Sr. Associate is an associate with a moderate level of technical expertise and experience. May perform complex activities outside of routine manufacturing operations commensurate with their experience and training. Will participate in the day to day operation of a cGMP compliant Manufacturing facility. Responsibilities include performing basic to complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls under limited supervision. Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities. | 11/20/2019 |
| 13196 | Thermo Fisher Scientific Foster City, CA Labware Technician I HS Diploma/GED Exp: 0-2 years in cGMP environment |
This position is focused on service delivery excellence for UnityTM Lab Services. Specific activities relative to the job function could include: laboratory glassware and inventory management. This position will utilize the basic functionality of systems and equipment relevant to the job function, such as: industrial glasswasher, sterilizers, and ovens. Strong communication skills are also required | 11/20/2019 |
| 13197 | Thermo Fisher Scientific Foster City, CA Labware Technician II HS Diploma/GED Exp: 0-2 years in cGMP environment |
This position is focused on service delivery excellence for UnityTM Lab Services. Specific activities relative to the job function could include laboratory glassware and inventory management. This position will utilize the basic functionality of systems and equipment relevant to the job function, such as: industrial glasswasher, sterilizers, and ovens, Microsoft Office suite. Strong communication skills are also required. | 11/20/2019 |
| 13198 | Thermo Fisher Scientific Cincinnati, OH QC Scientist I BS/BA in physical sciences, chemistry or biology preferred Exp: 0 years required |
Conducts routine chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods. Executes validated test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, and dissolution by HPLC, GC, dissolution, spectroscopy, and traditional quantitative analysis, utilizing HPLC, GC, LC/MS, dissolution, spectroscopy, and/or traditional wet chemical testing. Recognizes and reports out-of-specification or unexpected results and non-routine analytical and product problems. Performs daily instrument calibrations / verifications as required. | 11/20/2019 |
| 13199 | Thermo Fisher Scientific Eugene, OR Manufacturing Operator I HS Diploma/GED or AS/AA preferred Exp: 0 years required, lab experience a plus |
Operate processing and packaging equipment. Equipment includes: balances, labelers, band sealers, pumps, filtration systems, and other packaging equipment. Weigh, measure and check raw materials with assistance of computer interface to assure batches manufactured contain proper materials and quantities. Calibrate/operate semi-automated and automated manufacturing equipment. Complete and maintain Quality Records in compliance with regulatory requirements, GMP’s and standard operating procedures. | 11/20/2019 |
| 13200 | Thermo Fisher Scientific Eugene, OR Manufacturing Operator I HS Diploma/GED or AS/AA preferred Exp: 0 years required, lab experience a plus |
Operate processing and packaging equipment. Equipment includes: balances, labelers, band sealers, pumps, filtration systems, and other packaging equipment. Weigh, measure and check raw materials with assistance of computer interface to assure batches manufactured contain proper materials and quantities. Calibrate/operate semi-automated and automated manufacturing equipment. Complete and maintain Quality Records in compliance with regulatory requirements, GMP’s and standard operating procedures. | 11/20/2019 |
| 13201 | Invivoscribe San Diego, CA Manufacturing Associate I/II BS in sciences Exp: 1+ years in GMP lab |
As a Manufacturing Associate I/II for Invivoscribe you will assist with all aspects of production, including the production of master mixes, controls and assay kits. You will contribute to the drafting and review of new documents, including SOPs, Batch Records and Purchasing Specifications. Details include: Oversee, perform, plan and schedule production. Work with suppliers of core raw materials to ensure quality, quantity, price and availability. Create, review and revise production documents. Implement and train on the use of those documents. Participate in the production of master mixes and ASR, reconstitution of oligonucleotides, controls, reference standards and general purpose reagents by following manufacturing batch records, work instructions, standard operating procedures, forms and validated Excel spreadsheets. | 11/20/2019 |
| 13202 | Invivoscribe San Diego, CA Research & Development Associate I/II BS in technical/science field Exp: 1+ years in lab |
As a Development Associate I/II at Invivoscribe you are responsible for generating and documenting laboratory data with direct supervision. Your performance will contribute to a quality data generation in a regulated environment following good laboratory practices. More specifically: Support development projects that can include generating analytical data for an FDA submission. Use laboratory techniques such as PCR, gel and capillary electrophoresis, aseptic technique for mammalian cell culture, magnetic beads purification, DNA quantification and NGS. Execute and document experiments that support the development of diagnostic reagents and assays. Experimental design will include all of the appropriate controls. | 11/20/2019 |
| 13203 | Invivoscribe San Diego, CA Quality Control Laboratory Associate I/II BS in sciences Exp: 1+ years in GMP lab |
As a for a Quality Control Laboratory Associate I/II at Invivoscribe you will be responsible for receiving samples and performing data entry for specimens received as well as performing all aspects of clinical laboratory patient testing. More specifically: Test raw materials in process and final product and generate testing data. Releases products to QA for final approval. Ensure that all customer complaints and inquiries are resolved. Conduct and maintain the real time stability study testing. | 11/20/2019 |
| 13204 | Medical Diagnostic Laboratories, LLC Broken Arrow, OK Entry Level Sales Executive BS/BA Exp: 0-2 years |
As a Entry Level Sales Executive, you will be responsible for maintaining and growing a client base of both hospital and physician customers for MDL. Responsible for achieving annual sales and profit objectives for a defined territory. Obtain new business and exceed annual territory sales budget each year by presenting new test information, up selling and seeking out new sources of revenues from clients. Develop and present personalized sales presentations to professional audiences (physicians, laboratory staff, clinics and group practices); demonstrate how MDL's technical features and services could benefit the practice and help medical personnel provide quality patient care. | 11/20/2019 |
| 13205 | Medical Diagnostic Laboratories, LLC Multiple Locations, na Entry Level Sales Executive BS/BA Exp: 0-2 years |
As a Entry Level Sales Executive, you will be responsible for maintaining and growing a client base of both hospital and physician customers for MDL. Responsible for achieving annual sales and profit objectives for a defined territory. Obtain new business and exceed annual territory sales budget each year by presenting new test information, up selling and seeking out new sources of revenues from clients. Develop and present personalized sales presentations to professional audiences (physicians, laboratory staff, clinics and group practices); demonstrate how MDL's technical features and services could benefit the practice and help medical personnel provide quality patient care. | 11/20/2019 |
| 13206 | Invivotek Hamilton, NJ Research Associate - Animal Science/In-vivo BS in life sciences Exp: 1-2 years with rat/mouse handling |
We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 11/20/2019 |
| 13207 | Invivotek Hamilton, NJ Vivarium Technician HS Diploma/GED Exp: 0-2 years |
We are seeking a motivated and talented Research Associate to perform laboratory assays for validation of potential drug development targets and characterization of pharmacological compounds. The Research Associate should have excellent laboratory skills to conduct in vitro bioassays on murine tissues and primary cells. Experience with tissue culture techniques and primary cell-based assays are required with a variety of readout technologies including flow cytometry, RT-PCR and ELISA. Excellent communication skills and motivation to learn are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 11/20/2019 |
| 13208 | Saptalis Pharmaceuticals Hauppage, NY Analytical Scientist/Chemist BS in pharmacy, analytical chemistry, or related Exp: 0-3 years |
Develop analytical methods for actives, degradation and impurities, preservatives, and residual solvents in the new drug products.Perform analytical validation experiments per approved method validation protocols. Perform method verification and supplemental validation studies for active pharmaceutical ingredients and excipients. Perform release testing on actives, excipients, and packaging components to be used in GMP batch manufacturing. etc. | 11/19/2019 |
| 13209 | Sciecure Pharma Monmouth Junction, NJ QC Data Review Specialist BS in chemistry or related Exp: 1-2 years |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. Responsibilities: Review of documentation generated during method validation, method verification, stability testing, routine testing and other analyses. Review documentation, results and reports from raw material and finished product analysis for accuracy and completeness. etc. | 11/19/2019 |
| 13210 | Seattle Genetics Bothell, WA Research Associate I BioProcess Development BS in biology, chemical engineering, or related Exp: 1+ year(s) |
The BioProcess Development Department at Seattle Genetics is seeking a Research Associate to participate in the cell culture and purification efforts to support process development for our antibody and antibody-drug conjugate programs. Responsibilities: Generate monoclonal antibody (mAb) in support of Research and Process Sciences Program development. Responsible for all stages of mAb generation, from thaw of cryogenically stored vials through filling final formulated intermediate. etc. | 11/19/2019 |
| 13211 | Seattle Genetics Bothell, WA Research Associate II/III Pharmaceutical Sciences MS in pharmaceutical sciences, chemistry, biology, or related Exp: 0-2 years |
The Pharmaceutical Sciences group at Seattle Genetics is seeking a highly motivated research associate to support development of therapeutic antibody-drug conjugates. This person will play a critical role in the formulation and drug product process development of a novel pre-clinical ADC. The ideal candidate will have working knowledge of biologics formulation development and experience in common analytical techniques, as well as strong critical thinking skills and the ability to design, execute, and draw conclusions from experimental studies with managerial guidance. The ideal candidate should have a background in formulation development or analytical biochemistry or a related discipline, good interpersonal skills, and an ability to work effectively in intra-departmental teams to achieve program goals. | 11/19/2019 |
| 13212 | Sedia Biosciences Portland, OR QC Technician AS Exp: 1 year |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. Demonstrates a high level of independent judgment and discretion in the timely identification, investigation and resolution of events impacting the Quality of products and processes. etc. | 11/19/2019 |
| 13213 | Sedia Biosciences Portland, OR Manufacturing Technican AS in biology, chemistry, or related Exp: 1 year |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. The Manufacturing Technician will adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance. etc. | 11/19/2019 |
| 13214 | Sekisui Xenotech Kansas City, KS Research Assistant BS in a biological or chemical science Exp: 1+ year(s) |
Sekisui XenoTech, LLC is currently hiring for a Research Assistant for our Enzyme Incubations Team within the Program Execution department. The Research Assistant assists with routine laboratory functions including diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintains inventory of supplies, and various other responsibilities. Essential duties and responsibilities include, but are not limited, to the following: Design and conduct routine and atypical experiments. Maintains laboratories and equipment and performs minor repairs on equipment, with supervision. etc. | 11/19/2019 |
| 13215 | Seven Bridges San Francisco, CA Bioinformatics Support Engineer BS/MS in bioinformatics or related Exp: 1 year |
As a Bioinformatics Support Engineer you will be exposed to a wide range of translational applications and will work and learn from experts spanning numerous disciplines from informatics through cloud optimization and clinical data. You will work back to back with various members of our support and bioinformatics teams, helping our clients overcome obstacles they encounter. You will diagnose, resolve and explain issues and questions raised by our clients. Main responsibilities: Understand each client’s use case and their bioinformatics data processing pipelines. Debug, troubleshoot and resolve client issues associated with bioinformatics tools on the Seven Bridges platform. etc. | 11/19/2019 |
| 13216 | Silicon Therapeutics Boston, MA Research Associate, Software Engineering BS in engineering or computer science Exp: 1-2 years |
Silicon Therapeutics is seeking a highly motivated Software Engineering Research Associate who wants to work in a multi-disciplinary organization with the aim of treating challenging diseases. Job Responsibilities: Build software infrastructure to support platform development. Implement and maintain software engineering best practices. Ensure scalability, extensibility, and portability of platform code. Integrate and maintain databases for storage and access of results. Scripting and workflow development for scientific applications. | 11/19/2019 |
| 13217 | Silicon Therapeutics Boston, MA Research Associate, Machine Learning BS/MS in computer science, mathematics, engineering or related Exp: 1-6 years |
Silicon Therapeutics is seeking a highly motivated Research Associate, Machine Learning who wants to work in a multi-disciplinary organization with the aim of treating challenging diseases. Job Responsibilities: Work with a multi-disciplinary team (e.g. chemists, biologists, biophysicists) to discover novel medicines for challenging disease targets. Apply machine learning techniques to real-world drug discovery problems. Develop methods to improve the robustness of predictions from molecular dynamics simulations and quantify uncertainties associated with free energy simulations. Build state of the art machine learning infrastructure and workflows for molecular design. Work closely with bench scientists to understand critical project bottlenecks and how machine learning can help. | 11/19/2019 |
| 13218 | Simbex Lebanon, NH Test Engineer AS/BS in engineering Exp: 1-3 years |
The Test Engineer will be responsible for component and system testing throughout the product life cycle from development through release for products in the consumer health and medical device markets. The Test Engineer will work closely with project and cross-functional teams to help develop and execute test plans. The ideal candidate is self-motivated, detail oriented, and quick learner who can work in a fast-paced environment and values quality and accountability. etc. | 11/19/2019 |
| 13219 | Simbex Lebanon, NH Systems Engineer BS in mechanical or electrical engineering or related Exp: 0-3 years |
The Systems Engineer will be responsible for supporting every phase of the product development life cycle process in order to deliver high-quality products in the consumer and medical device markets. The Systems Engineer will work with the electrical, software, mechanical, product technical support, and quality teams to help develop, integrate, and test sub-assemblies into product. The ideal candidate has broad skills but deep knowledge/skills in one area, and is able to blend human-centric design with sound engineering principles across a wide range of engineering domains with a focus on quality and willingness to wear many hats. etc. | 11/19/2019 |
| 13220 | Smith & Nephew Oklahoma City, OK Quality Engineer BS Engineering/Science Exp: Entry level |
This position will be responsible for ensuring the effective investigation of devices and information supplied through the complaint management process, as well as the facilitation of actions identified to improve device quality, reliability, customer experience and patient safety. This position will participate in the identification and implementation of complaint management system improvements, including updates to procedures and forms used in the investigative process. The role may support multiple business sites both remotely and through on-site visits as needed. etc. | 11/19/2019 |
| 13221 | Smith & Nephew Memphis, TN Quality Assurance Inspector I HS diploma or related Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. Essential Responsibilities: Inspect raw materials, components, assembled product, semi-finished product & finished product per inspection procedures/drawings and to print specifications. Utilize attribute and variable measuring equipment/gauges as well as mating parts to determine as found/as left conditions of product. Support the qualification/validation processes for company product. etc. | 11/19/2019 |
| 13222 | Smith & Nephew Oklahoma City, OK Bench Technician I HS diploma or related Exp: 0-3 years |
Performs routine assembly and/or rebuilding of electromechanical medical instruments and assemblies using released procedures, drawings, blueprints, etc.. to meet established quality and performance metrics. Performs functional testing of assemblies/instruments. etc. | 11/19/2019 |
| 13223 | Smith & Nephew Andover, MA Quality Assurance Engineer I BS in engineering Exp: 1-3 years |
Support, and sustain elements of Smith & Nephew’s quality system through procedure generation, training, auditing, and technical support. Leading and supporting quality project initiatives. This position provides support and services in CAPA, complaints, validations, audits, quality holds, calibration and various other requirements of the medical device (US & International) regulations for R&D, Process Engineering, Manufacturing, Quality, and Regulatory plus any quality system support required. etc. | 11/19/2019 |
| 13224 | Smiths Medical Southington, CT Team Technician 3rd Shift HS diploma/AS Exp: 1-2 years |
The Team Technician is responsible for ensuring the correct operation of automatic and semi-automatic assembly production equipment in accordance with governing documentation. This person will also initiate action to prevent the occurrence of nonconformances related to the product and equipment. Additionally, this role will identify and record problems relating to the product, process and or quality system. The Team Technician will also initiate recommendations, provide solutions, and verify the affectivity of continuous operational improvements. | 11/19/2019 |
| 13225 | Solid Biosciences Cambridge, MA Contract QC Associate AS/BS Exp: 1-2 years |
Reporting to the Solid Quality Control (QC) Unit, the QC Associate is responsible for day to day operations related to sample submission and data management in support of QC GMP and cross-functional development. The candidate will maintain documentation in accordance with internal data entry, analysis and trending SOPs. In addition, coordinate domestic and international biologic sample shipments (at room temperature, on dry ice, or in liquid nitrogen) according to applicable guidelines. etc. | 11/19/2019 |
| 13226 | Sorrento Therapeutics San Diego, CA Research Associate II BS/MS in immunology, molecular biology or related Exp: 0-2 years |
Sorrento Therapeutics’ is seeking an experienced Research Associate who will be responsible for the development and implementation of in vitro functional T cell assays to support pre-clinical validation of CAR-T cellular therapies against cancer. The individual must have knowledge and hands on experience in CAR-T, cell culture, Flow cytometry and T cell biology. WHAT YOU’LL DO: Design and execute experiments for development of preclinical CAR-T therapies. Isolate, expand, and manipulate T cells. Perform in vitro functional assays measing cellular activation, cytokine release, proliferation and killing. etc. | 11/19/2019 |
| 13227 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I BS/BA in a biological or chemica science. Exp: 0-1+ year(s) |
We are currently seeking a Downstream Manufacturing Associate I. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. This position will also be responsible for supporting the inventory control for the downstream group. etc. | 11/19/2019 |
| 13228 | Sorrento Therapeutics San Diego, CA Manufacturing Associate II BS/MS in a biological or chemical science Exp: 1+ year(s) |
We are currently seeking a Downstream Manufacturing Associate II. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. An essential component of this position will be an understanding of cGMP methodologies: SOP’s, batch record preparation and execution, deviation control and general clean room maintenance. This position will also responsible for supporting the inventory control for the downstream group. etc. | 11/19/2019 |
| 13229 | Spectrum Pharmaceuticals Irvine, CA Clinical Trials Assistant BS in a life science Exp: 1-2 year |
Responsibilities: Provide support to the Clinical Trial Managers and Clinical Research Associates in clinical trial conduct via preparation, distribution, and tracking of study supplies, mass mailings, copying, data entry, etc. Demonstrate superior communication and organizational skills in addition to the technical skills required for overseeing clinical studies. Recognize the urgency of meeting established schedules and be able to prioritize tasks and time to meet those schedules. Help manage and report on the conduct of clinical studies, as directed. Help identify and select trial sites. Conduct qualification, initiation, interim monitoring close-out visits, and perform drug accountability (approximately 25% travel required). etc. | 11/19/2019 |
| 13230 | SQZ Biotech Watertown, MA Engineer/ Sr. Engineer BS/MS in bio, biomedical, or chemical engineering or related Exp: 0-2 years |
We are seeking a highly motivated Engineer/ Sr. Engineer to join our Process Development and Manufacturing team. The candidate will support process development efforts for novel cell therapy products. The candidate will perform hands-on laboratory work, data analysis, develop and maintain technical documentation, and collaborate with internal and external terms such as vendors to ensure successful execution of key development studies. The incumbent will also support manufacturing for technology transfers at CMOs and on-going cGMP production of clinical products. etc. | 11/19/2019 |
| 13231 | Integer Trenton, GA Manufacturing Engineer I -1st shift BS Exp: 0-3 years related |
Manufacturing Engineer providing basic engineering support for existing or new products. Learning to use professional concepts. This position will provide hands-on engineering support for existing products and products transitioning from New Production Introduction (NPI) to manufacturing. | 11/17/2019 |
| 13232 | Integer Plymouth, MN Design Engineer BS/BA in related field Exp: 0-3 years related |
Initiates, directs and manages the design, development, constructing and modification of products and processes from conception to implementation. Works closely with other departments to coordinate design engineering activities. Reviews, initiates or approves engineering drawings, layouts, changes orders and specifications. | 11/17/2019 |
| 13233 | Integra LifeSciences Mansfiled, MA Associate Product Development Engineer BS in engineering (electrical/computer) Exp: 0-3 years in product design/new product development |
The Engineer will participate in projects of varying scope and complexity across Integra with a focus on the Neuro Critical Care and will be responsible for the software and electrical design aspects of a project, interacting with external design and development partners, participating on cross-functional project team through all phases of the product development process, and assisting the technical team with planning, executing, documenting and communicating testing activities. The engineer will develop tools that will assist marketing and sales demonstrate Integra’s devices in an effective manner, and will develop test setups to automatize verification testing of different products. | 11/17/2019 |
| 13234 | Integra LifeSciences Cincinnati, OH Finishing Technician HS Diploma/GED Exp: 0-2 years in manufacturing |
Performs deburr, finishing, and cleaning in a job shop or high volume applications. Processes components to meet print and or geometric tolerance requirements. Responsible for the setup, operation and maintenance of production equipment needed for deburr, finishing, and cleaning operations, maintenance of proper documentation, and support of the manufacturing engineering function. Under close supervision, completes tasks as directed by SOPs, routers, prints, work instructions, and manufacturing schedules. | 11/17/2019 |
| 13235 | Integra LifeSciences Plainsboro, NJ Accoutant- Entry Level BA in accounting Exp: 0-3 years |
The accountant position is responsible for performing a combination of cost and general ledger accounting and financial close tasks, as assigned. Perform the monthly financial close process for the local ledger, including preparation of the monthly journal entries and balance sheet (cash, inventory, payables) and P&L account reconciliations, as assigned. Run various reports used to reconcile or analyze general ledger account balances. Assist in the preparation of the standard monthly management reports. Perform detailed monthly variance analysis on items in the P+L and balance sheet. | 11/17/2019 |
| 13236 | Integra LifeSciences Plainsboro, NJ Accoutant- Entry Level BA in accounting Exp: 0-3 years |
The accountant position is responsible for performing a combination of cost and general ledger accounting and financial close tasks, as assigned. Perform the monthly financial close process for the local ledger, including preparation of the monthly journal entries and balance sheet (cash, inventory, payables) and P&L account reconciliations, as assigned. Run various reports used to reconcile or analyze general ledger account balances. Assist in the preparation of the standard monthly management reports. Perform detailed monthly variance analysis on items in the P+L and balance sheet. | 11/17/2019 |
| 13237 | Integral Philadelphia, PA Biotechnology Marketing Associate BS/BA in sciences or marketing Exp: 1-2 years |
Plan and implement the creation of scientific and promotional materials in close collaboration with marketing, sales and scientific teams. Generate email blasts, website content, brochures, Google Adwords campaigns and slides. Create and update content to the company website using WordPress. Coordinate and organize team for appearances at industry conferences. Monitor and analyze effectiveness of marketing campaigns and website design | 11/17/2019 |
| 13238 | Integral Philadelphia, PA Business Development Associate MS or MBA Exp: 0-2 years in tech transfer, consulting or product commercialization |
Our company is in an exciting growth phase where we are launching new products and reaching new markets. To support our growth, we seek a Business Development Associate to help launch new partnerships, businesses, and growth strategies. Successful candidates will also be involved with our marketing and sales teams to assist with strategic growth plans. | 11/17/2019 |
| 13239 | Integral Philadelphia, PA Laboratory Instrumentation Engineer BS/BA Exp: 0-2 years in lab support/equipment |
We seek an associate to join us as our Laboratory Instrumentation Engineer. This is a specialized position that will be responsible for maintaining and using flow cytometers, robotic liquid handlers, and other equipment. You will be part of the team that supports lab operations, with opportunities for conducting experiments and leadership of the team. | 11/17/2019 |
| 13240 | Integral Philadelphia, PA Research Associate I BS/BA in biology or bioengineering Exp: 1-2 years in lab/cell culture experience |
We seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. Conduct laboratory research and support general R&D efforts for customer-based biomedical research. Projects may involve cell culture, virology, DNA preparation, and liquid-handling automation. Perform cell-based assays (Western blot, ELISA, immunofluorescence, flow cytometry) | 11/17/2019 |
| 13241 | IDT Morrisville, NC Future Lab Technician Roles Early 2020 BS/BA in sciences Exp: 0 years |
Synthesizes oligos on various synthesizer platforms. Cleaves and deprotects oligos utilizing appropriate methods. Quantifies and samples oligos for quality control tests. Attaches modifications utilizing various techniques. Adheres to safety regulations, lab SOPs, and contamination controls. | 11/17/2019 |
| 13242 | IntegrityBio Camarillo, CA Research Associate BS in biochemistry, chemistry, or biological sciences Exp: 1-5 years |
To meet the growing demand on the part of our clientele regarding the outsourcing of projects and technologies, we are seeking candidates for the position of Research Associate I or II in Research and Development (R&D). Assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision. Analyzes, records, and reports the results and conclusions for laboratory experiments. Summarizes and interprets data. The candidate should also be open to learn new laboratory techniques and work under the guidance of experienced researchers. | 11/17/2019 |
| 13243 | Intrexon Davis, CA Research Associate, Plant Traits BS or MS Exp: 1-3 years in molecular biology/plant biology |
Intrexon Corporation is seeking a highly motivated Research Associate, Plant Traits with molecular biology skills for our growing Agricultural Biotechnology Division (ABD) at Davis, California. The candidate will join a team to work on innovative technology to develop various traits in crops. The successful candidate will have hands-on experience with molecular techniques as well as supporting the senior scientist to develop other methodology to enable high-through-put, low-cost genotyping in multiple crops. Strong technical, organizational, and communication skills, as well as the ability to develop creative solutions to challenging problems in a fast-paced, milestone driven company, are essential. | 11/17/2019 |
| 13244 | Intrexon South San Francisco, CA Research Associate I or II, Pilot Plant Ops BS in sciences, engineering or related Exp: 0-3 years industry experience |
We are seeking a talented Research Associate (level determined by candidate experience), Pilot Plant Operations for our Industrial Products Division (IPD) located in South San Francisco. The Research Associate will be responsible for operating pilot plant equipment, performing maintenance tasks, and have the skill set to thrive in a dynamic team environment. | 11/17/2019 |
| 13245 | Intuitive Sunnyvale, CA Manufacturing Trainer 1 HS Diploma/GED Exp: 12 months in ISI product manufacturing |
Partner with Manufacturing to develop and sustain a well-trained and flexible workforce through hands-on training, mentoring, and formal certification. Maintain accurate manufacturing and training documentation to ensure the effectiveness of the training process. Develops and prioritizes quarterly training plans based on input from Production and Training Supervision. Conducts training, mentoring and formal certification of production technicians in accordance with S & V Training DOP’s and Manufacturing Process Instructions. | 11/17/2019 |
| 13246 | Intuitive Sunnyvale, CA MRMA Repair Technician AA/AS Exp: 1-3 years related experience |
A Mechanical RMA Repair Technician II works under general direction, follows oral and/or written instructions, and performs repair and testing processes to produce tested electro-mechanical assemblies or associated sub-assemblies. Performs some-what complex tasks in preparation for repair and testing. Is able to verify assembly documentation accuracy, read engineering drawings etc. Sets up and operates machines/equipment /fixtures needed to perform repair and testing processes. | 11/17/2019 |
| 13247 | Intuitive Los Angeles, CA da Vinci Clinical Territory Associate- North Los Angeles BS/BA in sales or related Exp: 1 year of sales or leadership experience |
The Clinical Territory Associate (CTA) will work closely with the Clinical Sales Manager to gain knowledge in all aspects of our business to include technical, clinical, and sales. He or She will train to be a da Vinci® Surgery technical and sales expert across all primary surgical specialties to develop surgical robotics programs in the assigned territory. During the first year of the job, the CTA will focus on the technical and clinical aspect of the job, and during the second year of the job, the CTA will progress and begin to focus on the sales aspect of the job. The CTA will have the opportunity to support a specific region by maximizing the utilization of installed da Vinci® Surgical Systems by leading product demonstrations/in-services and sales activities. | 11/17/2019 |
| 13248 | Integer Minneapolis, MN Associate Quality Technician HS Diploma or AS/AA Exp: 0-2 years in manufacturing |
The primary purpose of this position is to perform standardized measurements of parts in-process involving prescribed measurement tools under guided supervision. This position will work to maintain elements of Quality Management Systems (QMS) in accordance with ISO 13485 and FDA 21 CFR 820 requirements as well as company protocols. | 11/17/2019 |
| 13249 | Integer Chaska, MN IT Service Delivery Technician AS/AA or BS/BA Exp: 0-3 years related |
The primary purpose of this position is to support and maintain all IT hardware and software; including desktops, laptops, printers, mobile devices, phones, peripherals and client software. Provides direct support to office, manufacturing and engineering environments in person, over the phone and via e-mail to local and remote Associates. Participates in the development of IT support processes, tools and documentation for company. | 11/17/2019 |
| 13250 | Integer Brooklyn Park, MN Manufacturing Team Member I HS Diploma/GED Exp: 0-2 years related |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Adheres to GB Core Beliefs, Behavioral Based Safety process and Greatbatch Associate Quality Policy. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). | 11/17/2019 |
| 13251 | Integer Brooklyn Park, MN Manufacturing Team Member I HS Diploma/GED Exp: 0-2 years related |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Adheres to GB Core Beliefs, Behavioral Based Safety process and Greatbatch Associate Quality Policy. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). | 11/17/2019 |
| 13252 | Integer Chaska, MN Manufacturing Team Member I HS Diploma/GED Exp: 0-2 years related |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Adheres to GB Core Beliefs, Behavioral Based Safety process and Greatbatch Associate Quality Policy. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). | 11/17/2019 |
| 13253 | ICON Boston, MA Laboratory Assistant - Full Time Days HS Diploma/GED Exp: 1 year lab experience |
As a Laboratory Assistant will assist and aid the technical staff with handling and accounting for biological lab specimens, reagent inventory, and any other relevant tasks. Assists with retrieval and set up of samples for analysis. Receives samples from Sample Management and segregate and distribute to the lab as per standard operating procedure. Monitor Sample Logistic Scan/pending list and search for lost samples. Troubleshoot issues with Sample Management when required. Member of the Lost sample Team. | 11/16/2019 |
| 13254 | ICON North Wales, PA Clinical Research Associate HS Diploma/GED Exp: 18+ months as CRA |
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results. | 11/16/2019 |
| 13255 | ICON Farmingdale, NY Laboratory Study Start-Up Specialist BS Exp: 1 year in clinical trails, lab, etc. |
Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/16/2019 |
| 13256 | ICON Lexington, KY DPC Assistant HS Diploma/GED Exp: 1 year in medical office/admin |
The DPC Assistant will provide support services (logistical, technical and administrative) to the Direct to Patient Contact (DPC) project team all along the project, while complying with the deadlines, budgets, quality and regulatory requirements defined for each project. For each project, the Direct to Patient Contact Manager (DPCA) works under the technical and functional supervision of the dedicated Direct to Patient Contact Manager (DPCM). | 11/16/2019 |
| 13257 | ICON North Wales, PA Configuration & QC Spec I BS Exp: 1 year in clinical trails, lab, etc. |
Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/16/2019 |
| 13258 | ICON Portland, OR Laboratory Assistant (Maintenance Tech) HS Diploma/GED Exp: 1 year in operations/scientific equipment |
The Lab Assistant (Maintenance Technician) supports the activities of Production, Development, and the Clinical Laboratories. The Maintenance Technician performs equipment maintenance and cleaning, qualification, assists in the development of equipment specifications and other equipment or facility related activities to ensure proper qualification, function and reliability. | 11/16/2019 |
| 13259 | ICU Medical Austin, TX Technician I, Biological Quality/Environmental Quality BS/BA in microbiology/biological sciences Exp: 1 year general micro course with lab, or 1 year working experience |
The BQ/EQ Scientific Technician I is responsible for performing routine and non-routine testing in support of all aspects of the manufacturing operations including but not limited to the utility systems, sterilizer systems, incoming raw materials, in-process product solutions and final product solutions while adhering to safety, standard operating procedures (SOPs), standard test methods (STMs) and specifications, current good manufacturing practices (cGMP), standard laboratory practices (SLP), current good documentation practices (cGDP) and plant policies/guidelines. | 11/16/2019 |
| 13260 | IDEXX Memphis, TN Histology Laboratory Technician HS Diploma/GED, higher degree preferred Exp: 1-5 years |
You will be using microtomes, processors, embedding centers, automatic slide stainers and other diagnostic tools to perform tissue analyses that diagnose animal illnesses and diseases in support of veterinarian animal treatment. You will be responsible for transforming a tissue sample into a slide that will be read by a board-certified veterinary anatomic pathologist. It is expected you will follow SOPs (Standard Operating Procedures) and maintain a safe working environment. | 11/16/2019 |
| 13261 | IDEXX Westminster, CO Sample Management Technician HS Diploma/GED, higher degree preferred Exp: 0-1 years |
The Sample Management Technician receives and prepares samples for laboratory analyses and tests. Prepares samples on slides or other testing format, records required information and sends to appropriate specialty lab area. May be cross-trained to perform basic Laboratory Technician duties, such as performing less complex tests. May be responsible for various support activities, including maintaining supply inventory, record-keeping, cleaning, clerical tasks, supply shipping and receiving, mail distribution and other related duties. Collects and prepares samples as requested/ required for R&D project teams. | 11/16/2019 |
| 13262 | IDEXX Westminster, CO Medical Laboratory Technician - Parasitology HS Diploma/GED, higher degree preferred Exp: 0-1 years |
The Medical Laboratory Technician performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform variety of customer service activities for internal and external customers. Testing cell-related components of blood samples to enumerate and identify their cellular components, including the microscopic evaluation of blood smears and the use of automated and manual counting techniques. Processing blood and body fluids for microscopic examination by pathologists. Includes slide preparation and staining, utilizing manual and automated counting techniques. | 11/16/2019 |
| 13263 | IDEXX West Sacramento, CA PCR Laboratory Technician Certified Vet Tech or Medical Lab Tech Exp: 0-1 years |
You will be using automated analyzers, microscopes, and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries, and diseases in support of veterinarian animal treatment. You will be responsible for setting up and running lab tests, and reading and releasing results according to SOPs (Standard Operating Procedures). You can expect to specialize in one or more of the following areas: | 11/16/2019 |
| 13264 | Imbed Biosciences Madison, WI Production Technician, Medical Device Manufacturing BS in sciences Exp: 1-4 years in chemistry/biological lab |
Work with Medical Device Production team in a moderate-volume commercial laboratory to fabricate polymeric films, perform and assist in daily laboratory tasks and work flow, maintain and edit standard operating procedures and work instructions, record data, write reports and communicate results. Ensure quality control of materials and end products of the company in a consistent manner. | 11/16/2019 |
| 13265 | Immucor Norcross, GA Medical Laboratory Technologist I AS/AA or BS/BA Exp: 6-12 months related experience |
Immucor is seeking a Medical Laboratory Technologist to join our Quality Laboratory team. The Medical Laboratory Technologist is responsible for performing laboratory testing (including potency, specificity, reactivity and hemagglutination assays) and chemical evaluations (including protein, absorbance, chloride, osmolality, and pH) of Immucor products according to approved Standard Operating Procedures (SOP’s) within defined timeframes. | 11/16/2019 |
| 13266 | Immucor Warren, NJ Manufacturing Associate AS/AA Exp: 1 year in cGMP manufacturing |
As the Manufacturing Associate, you will perform setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency. Performing the following activities in a quality focused cGMP manufacturing environment: Formulating custom bulk reagents - involves working with pipettes and balances. Support BeadChip carrier assembly - involves both manual and automated equipment processes. Following detailed work instructions, forms, and SOPs | 11/16/2019 |
| 13267 | Immucor Norcross, GA Medical Laboratory Technologist I AS/AA or BS/BA Exp: 6-12 months related experience |
Immucor is seeking a Medical Laboratory Technologist to join our Quality Laboratory team. The Medical Laboratory Technologist is responsible for performing laboratory testing (including potency, specificity, reactivity and hemagglutination assays) and chemical evaluations (including protein, absorbance, chloride, osmolality, and pH) of Immucor products according to approved Standard Operating Procedures (SOP’s) within defined timeframes. | 11/16/2019 |
| 13268 | Immune Technology Corp New York , NY Sales Associate BS/BA in life sciences Exp: 1 year of sales/marketing experience |
Full/part time position, responsible for ensuring customer retention through account management and increasing revenue through marketing activities and generation of sales leads. Establishing and retaining customer relationships primarily through phone, e-mail and personal visit . Delivering requested documents, literature, and information to customers. Organizing and maintaining a database of customers and sales leads | 11/16/2019 |
| 13269 | Immunomedics Morris Plains, NJ QC Sample Coordination Technician - (2nd shift) BS/BA in sciences Exp: 0-2 years |
The primary purpose of this second shift position is to provide support to the sample management group in a QC laboratory setting in support of commercial manufacturing. Responsibilities of the QC Sample Coordination Technician include collating receipt of samples and coordination of testing, preparation of samples using aseptic technique, organizing and tracking lot release data, submission of samples to contract testing laboratories and tracking sample custody. Activities include equipment maintenance, coordinating with Shipping and Receiving, and receipt of test results from contract laboratories. | 11/16/2019 |
| 13270 | Immunomedics Morris Plains, NJ Manufacturing Specialist I AS/AA or BS/BA in engineering or sciences Exp: 0-2 years |
Responsible for pharmaceutical manufacturing in compliance with current Good Manufacturing Practice (cGMP). Ensures consistent completion of all the planned manufacturing activities assigned to him/herself. Organize workplace to maximize the throughput and minimize risks of errors. Follow well defined procedures closely, with attention to detail. Operate manufacturing equipment according to well defined procedures. Daily monitoring of the process. | 11/16/2019 |
| 13271 | Imprimis RX Ledgewood, NJ Production Support Associate HS Diploma/GED Exp: 1 year in pharma, med devices or related |
The Production Support Associate is part of our production team. The Production Support Associate supports our production team by assisting in the main production area. Performs various routine production tasks under the guidelines of established SOP’s and CGMP regulations. Prepares components needed for production, such as washing vials, wiping of supplies needed for the clean room. Performs cleaning and disinfecting of manufacturing and clean rooms per established procedures. | 11/16/2019 |
| 13272 | Indigo Biosciences State College, PA Associate Scientist MS in biological sciences Exp: 0-5 years |
The successful candidates will have formal training and demonstrated technical proficiencies / expertise in one or more of the following areas: mammalian cell biology, mammalian toxicology, receptor biology, assay development, molecular biology, and/or biochemistry methods. | 11/16/2019 |
| 13273 | Indivior Austin, TX Specialty Pharmaceutical Sales Rep/Clinical Specialist (Austin) BS/BA Exp: 1+ year in pharma/medical/healthcare |
The Clinical Specialist is responsible for calling on practicing physicians, hospitals, clinics and other health-related organizations within an assigned territory. The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Accomplishments of these goals must comply with the terms and conditions outlined in the Company Policy and Procedure Manual. | 11/16/2019 |
| 13274 | Inova Diagnostics San Diego , CA Chemist I- Elisa Controls BS/BA in biological sciences Exp: 0-2 years in ELISA lab |
Participates in the activities associated with the manufacturing of ELISA reagents such as control, calibrator and HRP conjugate components in accordance with established procedures and schedules. Ensures supplies, testing components, raw materials and equipment required to meet manufacturing schedules are available. Alerts the supervisor of any material shortages, potential expiration date problems, equipment requirements and/or other circumstances, which may cause delays in the planned, manufacturing schedule. Maintains detailed Device History Records and/or any associated documentation for all manufacturing activities in accordance with current Quality Systems Regulations (QSRs). | 11/16/2019 |
| 13275 | Inova Diagnostics San Diego , CA Lab Assistant I HS Diploma/GED Exp: 0-4 years lab work experience |
Assists with the activities required to manufacture autoimmune diagnostic products by following established procedures. Major duties include the manufacturing of tissue sections and their placement onto glass microscope slides for use in Immunofluorescent Assay products. Participates in all activities associated with the manufacturing of the tissue sections and their placement onto glass microscope slides in accordance with written documentation and established procedures. Manufactures 8.5 eight-well ANA Plus Slides per hour after three months of training. 10 eight-well ANA Plus slides per hour within one year of employment. Thereafter, manufactures 10.5 slides per hour for eight-well slides and 21 slides per hour for four-well slides (all tissue types). Assists with the activities required to manufacture autoimmune diagnostic products by following established procedures. Major duties include the manufacturing of tissue sections and their placement onto glass microscope slides for use in Immunofluorescent Assay products. Participates in all activities associated with the manufacturing of the tissue sections and their placement onto glass microscope slides in accordance with written documentation and established procedures. Manufactures 8.5 eight-well ANA Plus Slides per hour after three months of training. 10 eight-well ANA Plus slides per hour within one year of employment. Thereafter, manufactures 10.5 slides per hour for eight-well slides and 21 slides per hour for four-well slides (all tissue types). Assists with the activities required to manufacture autoimmune diagnostic products by following established procedures. Major duties include the manufacturing of tissue sections and their placement onto glass microscope slides for use in Immunofluorescent Assay products. Participates in all activities associated with the manufacturing of the tissue sections and their placement onto glass microscope slides in accordance with written documentation and established procedures. Manufactures 8.5 eight-well ANA Plus Slides per hour after three months of training. 10 eight-well ANA Plus slides per hour within one year of employment. Thereafter, manufactures 10.5 slides per hour for eight-well slides and 21 slides per hour for four-well slides (all tissue types). | 11/16/2019 |
| 13276 | Inovio San Diego , CA Research Associate I, Preclinical (2 positions available) BS in biological sciences Exp: 0-1 years research experience |
The Research Associate I (RA) is responsible for performing in vitro and in vivo experiments as part of a team to support development of DNA-based vaccines and therapeutics prior to clinical development. The RA performs a variety of techniques, including treatment and sample collection, immunoassays, cell-based assays, flow cytometry, and cell line maintenance. The RA troubleshoots problems, reviews and documents results, and presents findings at departmental or company meetings. The RA performs general lab duties as needed. | 11/16/2019 |
| 13277 | Inovio Plymouth Meeting, PA Clinical Trial Associate BS in biological sciences Exp: 0-2 years in clinical trails monitoring/management |
The Assistant, Clinical Trials (CTA) is responsible for supporting, under the direct supervision of the supervisor/Clinical Project Lead (CPL), clinical trial execution, investigator sponsored research and program level activities as assigned within Clinical Operations at Inovio. This position assists in various tasks and projects related to clinical trials as well as basic, administrative duties. | 11/16/2019 |
| 13278 | Omnipod Salt Lake City, UT Intake Associate AS/AA Exp: 0-1 years working experience |
The primary responsibility of this role is to review and process clinical documentation promptly and accurately to ensure proper reimbursement from contracted payors. The Intake Associate will utilize this clinical documentation to perform benefit investigations as well as prior authorizations with our contracted payors. This role will work with all department functions and must have a thorough understanding of the reimbursement process, clinical guidelines and medical policies. | 11/16/2019 |
| 13279 | Omnipod Salt Lake City, UT Inside Sales OmniPod Associate AS/AA or BS/BA Exp: 0-1 years in medical devices/pharma/healthcare |
The Inside Sales - OmniPod Associate role is responsible for all patient communication during the sales process of starting patients on the OmniPod system. This role works closely and collaborates with the field sales and internal team members to provide the best patient experience possible. This role is responsible for communicating insurance benefit guidelines and cost share information with patients and assists them with their decisions regarding insulin pump therapy. | 11/16/2019 |
| 13280 | Omnipod Billerica, MA Associate SQA Engineer BS in software engineering/computer sciences Exp: 0-2 years in software QA |
This position assists in the software quality assurance efforts related to new product development and product modifications for the Research and Development group. The position is responsible for ensuring that new products have been effectively and efficiently verified and validated prior to their release for shipment and that these designs effectively meet documented and implied user needs and requirements. Software quality assurance efforts are lifecycle oriented beginning during product requirements development and continuing throughout its lifetime. | 11/16/2019 |
| 13281 | Omnipod Atlanta, GA Clinical Services Specialist BS/BA Exp: 0-2 years in clinical setting |
The Clinical Services Specialist (CSS) is primarily responsible for meeting all clinical initiative expectations. This responsibility will require extensive travel and extended stays in a field based territory to support open territory needs. The CSS will provide product sales, training, downloading and technical support in accordance with company policy. They will also in-service physicians, mid-level staff, CDE’s, and ancillary staff on the OmniPod Insulin Management System, build relationships with our customers, and skilled at selling and using the OmniPod Insulin Management System. | 11/16/2019 |
| 13282 | Omnipod Dallas, TX Clinical Services Specialist BS/BA Exp: 0-2 years in clinical setting |
The Clinical Services Specialist (CSS) is primarily responsible for meeting all clinical initiative expectations. This responsibility will require extensive travel and extended stays in a field based territory to support open territory needs. The CSS will provide product sales, training, downloading and technical support in accordance with company policy. They will also in-service physicians, mid-level staff, CDE’s, and ancillary staff on the OmniPod Insulin Management System, build relationships with our customers, and skilled at selling and using the OmniPod Insulin Management System. | 11/16/2019 |
| 13283 | Omnipod Acton, MA Business Analyst, Post Market Surveillance BS in sciences/engineering Exp: 1-3 years in data management/Quality systems |
This position is integral to supporting the department through complaint software enhancements, upgrades, report creation, data structure, and validation activities/documentation. The BA will be the primary connection to IT resources supporting the business unit. The BA will have a strong understanding of the business unit’s processes, context surrounding why the processes are in place, and what happens if processes are not functioning/followed. The BA will be an expert in the systems utilized by the business unit and understand the implications of system structure, how changes may impact systems, and how system data is utilized for reporting. | 11/16/2019 |
| 13284 | Immunomedics Morris Plains, NJ Quality Control Associate Scientist BS/BA in chemistry or related Exp: 1-3 years in biopharma or related |
The QC Associate Scientist, Raw Materials, is responsible for routine testing of incoming raw materials for release and adventitious virus safety testing of bioreactor harvests, both inhouse and at third party provider. This position includes responsibility for validation and technical transfer of test methods, including the preparation of validation protocols and reports, authoring technical reports, specifications for incoming raw materials and evaluation of change notifications. | 11/16/2019 |
| 13285 | Omnipod Billerica, MA QE Technician BS/BA in sciences/engineering Exp: 0-1 years |
This position will primarily work within the QC Lot Qualification group as an investigative technician to complete timely root cause investigations and work with Manufacturing and Engineering to drive process improvements. Must be quickly adaptive to changing priorities. This position will also support lot qualification testing and other QE supporting assignments when needed. This position will be based at 14 Progress Road in Billerica, MA with travel to our Acton, MA location as needed. | 11/16/2019 |
| 13286 | IDEXX Elmhurst, IL Sample Management Technician, FT Days HS Diploma/GED, higher degree preferred Exp: 0-1 years |
As a Sample Management Technician, you will receive and prepare samples for laboratory analyses and testing that diagnose various pet illnesses, injuries and diseases. You can expect to remove specimens from transport bags and split as needed for multiple testing. You will enter data about the specimens into a computer tracking system. You will also rack and bundle prepared samples for delivery to each testing department. In this role, accuracy, safety and quality are extremely important, so you will be expected to read, understand and follow applicable Standard Operating Procedures (SOP's), including safety and quality procedures. | 11/16/2019 |
| 13287 | Immucor Norcross, GA Manufacturing Technician BS/BA in biological sciences preferred Exp: 1-3 years in aseptic manufacturing preferred |
Your main duties as a Manufacturing Technician include the preparation of chemical solutions such as weighing chemicals (both liquid and dry) and mixing components according to Standard Operating Procedures (SOPs). The incumbent will also perform the preparation of diluents, dilution of product, pre-filtration and post-filtration of samples for culturing, and unit weight determination. | 11/16/2019 |
| 13288 | Immucor Norcross, GA Production Support Technician I HS Diploma/GED Exp: 1-3 months related experience |
We are seeking a Production Support Technician to provide day-to-day operations support for all manufacturing areas. Additional responsibilities include: Perform washroom activities, staging and set up bottles for production use and maintain inventory. Responsible for training on all procedures assigned, and has the ability to be cross trained to assist in other production areas or departments as needed. Assist in the review of documentation for assigned functions, equipment logs, and manufacturing records, etc. Follow GMP documents, SOPs, Manufacturing Records with strict adherence to safety and compliance regulations | 11/16/2019 |
| 13289 | Precision Biosciences Durham, NC Data Scientist - BioAnalytical Development MS in computer science, statistics, computional biology or related Exp: 0-2 years |
The Associate Scientist, Data Science works within the BioAnalytical Team at Precision Biosciences focused on the development of genome-edited allogeneic CAR-T therapeutics. The incumbent will play a lead role in the identification and implementation of existing and/or novel algorithms, analytical techniques and computational procedures to mine, clean, and interpret a wide variety of data derived from genomic, proteomic, metabolomic, and cellular phenotypic methods. This team member will be a part of our broader CMC organization which aims to drive technical excellence for the successful development of Precision Biosciences’ Cell and Gene Therapy Products, including allogeneic CAR-T cells, AAV viral vectors, and Lipid Nanoparticle-Encapsulated mRNA spanning a broad range of indications in immuno-oncology, infectious disease, and rare genetic disease. etc. | 11/12/2019 |
| 13290 | Precision Medicine Group Frederick, MD Biorepository Technician - Entry Level BS in related field Exp: Entry level |
Play a critical role in helping patients gain access to the treatment they need. This position is responsible for specimens in our state of the art Specialty Labs facility that have been collected by our clients who are managing clinical trials to secure the required approval for potentially life-saving patient treatments. Clinical trials depend on biological specimen samples being withdrawn and deposited on a continual basis. etc. | 11/12/2019 |
| 13291 | Precision Medicine Group Carlsbad, CA Biostatistician I – Clinical Trial Services MS in biostatistics/statistics Exp: Entry level |
What to expect day-to-day: Generating randomization schedules and providing sample size calculations. Providing input into development of case report forms (CRFs). Authoring and reviewing statistical analysis plans, including development of table and listing shells. Generating analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. Providing programming support and quality control for SAS Programs and other study documents. etc. | 11/12/2019 |
| 13292 | Precision Medicine Group Norton, MA Clinical Data Associate BS/MS Exp: Entry level |
How you will make a difference: Review, analyze, validate and maintain clinical trial data to ensure consistency, integrity and accuracy. Query data inconsistencies and update the databases by understanding standard operating procedures, client guidelines and regulatory agency guidelines. Perform User Acceptance Testing. Prepare Patient and Study Level Status/Metric reporting. Utilize dictionary coding such as MedDRA and WhoDrug. Generate data retrievals and summaries. | 11/12/2019 |
| 13293 | Precision Medicine Group Oakland, CA Associate Research Statistician - HEOR MS in economics, health services, biostatistics or related Exp: 1+ year(s) |
As Research Statistician, you will perform a wide range of activities including: literature reviews; analysis; preparing reports, slide decks and meeting notes; and quality assurance/review. You will independently complete, evidence synthesis projects, including: client management; systematic literature review (SLR); (network) meta-analysis; economic modeling; and dissemination of results. etc. | 11/12/2019 |
| 13294 | Precision Medicine Group Houston, TX Technologist – PBMC / IHC BS in medical technology, biology, or related Exp: 0-1 years |
As a Technologist, you will participate in simple and complex processing of tissue, PBMCs, blood and body fluids, both routine and non-routine procedures. You will work with scientists to carry out qualification of assays for new projects and be engaged in IF / IHC / Opal staining tasks. This position requires flexibility to work on different shifts as needed. etc. | 11/12/2019 |
| 13295 | Promega Madison, WI Quality Technician HS diploma or equivalent Exp: 1-3 year(s) |
JOB OBJECTIVE: Perform Quality inspection and analysis activities including: Receiving inspection of purchased components and materials in accordance with written procedures, statistical sampling plans, inspection standards and engineering drawings and specifications, using measuring equipment. In-process and finished device inspection and release activities in accordance with the Device Master Record. etc. | 11/12/2019 |
| 13296 | ProSciento San Diego, CA Clinical Data Associate BS in the life sciences Exp: Not necessary for BS candidates |
Under the supervision of the Associate Director, CRA Services, conducts site monitoring for clinical research studies according to ProSciento Standard Operating Procedures (SOPs) and ICH/GCP/GLP guidelines. Prepares monitoring reports and assists with query resolution. Performs duties in accordance with the company’s values, policies, and procedures. Essential Duties and Responsibilities include the following. Other duties may be assigned at the Company’s sole discretion. Responsible for all aspects of study site monitoring including site qualification visits, pre-study visits, site initiation visits, routine monitoring visits, and close-out visits of clinical sites. etc. | 11/12/2019 |
| 13297 | PTC Therapeutics South Plainfield, NJ Research Associate - Neuroscience BA/BS Exp: 1-2 year(s) |
Reporting to a PhD Scientist in the Neuroscience Group at PTC, the Research Associate is involved in performing experiments using a variety of techniques, including analysis of RNA, protein, electrophysiology on brain tissue and imaging of cells and tissue sections. The successful candidate will: Work collaboratively with other PTC researchers to execute experiments in a highly matrixed environment. Analyze and interpret data generated. Assure that timelines are adhered to through efficient time management. Communicate effectively within the research team and across functional areas. Present data at internal meetings. etc. | 11/12/2019 |
| 13298 | PTC Therapeutics Mountainview, CA Laboratory Technician/Research Assistant, Compound Management AS/BS in chemistry, biochemistry, or biology Exp: 0-2 years |
We are seeking a highly organized technician/research assistant to manage the proprietary compound collection at the PTC Mountain View Research Site. This individual will be a key member of the research group, providing samples to internal and external collaborators. Additionally, the compound management technician will perform routine chemical and biological assays to support various programs. The successful candidate will be almost pathologically detail-oriented and thrive performing high precision work. etc. | 11/12/2019 |
| 13299 | Pyramid Laboratories Costa Mesa, CA Manufacturing Technician No degree required Exp: 1 year |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. PRINCIPAL DUTIES: Familiar with related GMP procedures and requirements, as directly related to the position. Ensure that appropriate procedures and processes are utilized without unauthorized modifications. Ability to set-up, maintain and perform various manufacturing related activities as required for a GMP compliant Fill/Finish operation. etc. | 11/12/2019 |
| 13300 | Quick Biology Pasadena, CA Research Associate MS in biochemistry, molecular, or biological science Exp: 1-4 year(s) |
We are seeking a Research Associate I to perform sample preparation, RNA/DNA extraction, QC/QA, sequencing library construction and Illumina Hiseq sequencer operation in our sequencing team. The successful candidate should have knowledge of next-generation sequencing using the Illumina platform. The successful candidate should work somewhat independently to conduct laboratory experiments on NGS projects within well-defined guidelines; Ability to independently design and execute SOPs to meet project goals is essential. | 11/12/2019 |
| 13301 | Regeneron Tarrytown, NY R&D Associate - Neurodegenerative Diseases MS in neuroscience, biochemistry, biology or related Exp: 1+ year(s) |
We are seeking a talented and motivated R&D Associate / Specialist to join our highly dynamic neuroscience team. The successful candidate will be responsible for the design and execution of experiments to understand the mechanisms of neurodegenerative diseases, discover new therapeutic targets and validate novel therapeutic strategies. We are looking to recruit a candidate with in vitro experience and strong in vivo expertise in neuroscience and models of neurodegenerative disease. etc. | 11/12/2019 |
| 13302 | Repligen Waltham, MA Manufacturing Associate - ELISA AS/BS Exp: 1-2 year(s) |
This position is in Repligen’s ELISA group. The successful candidate will be responsible for the manufacture of ELISA kits and its components as well as in-process testing. The individual must be able to follow oral and written instructions accurately and complete tasks in a timely manner. Experience working in a GMP/ISO/document-controlled environment would be beneficial. Attention to detail and the ability to work in a team environment are essential. Candidates must be willing and able to learn new manufacturing processes as the company grows. | 11/12/2019 |
| 13303 | RTI Surgical Alachua, FL Materials Tech 1 HS diploma or equivalent Exp: Entry level |
The Materials Tech 1 position at RTI represents an entry level function. Employees will develop technical skills in their assigned areas, an understanding of the rules and regulations that RTI administers, and the basic operating approach at RTI including: reading, understanding, and following work instructions; working in a team environment; and learning to work with minimal supervision. POSITION SUMMARY: Performs daily activities in accordance with applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs). Unpacks, segregates, organizes, wraps, and packages various supplies and equipment. etc. | 11/12/2019 |
| 13304 | RTI Surgical Alachua, FL BMS Technician HS diploma or equivalent Exp: 1 year |
POSITION SUMMARY: Maintains accurate records of all specimens received or sent out of the laboratory. Completes test request forms and enters the information into the Laboratory Information System. Performs specimen preparation for testing and archiving. Makes determinations as to acceptability of specimens, and files appropriate specimen rejection forms and revision request forms when necessary. Performs non-licensed testing, interprets non-licensed testing results, and prepares reports. Performs quality control and quality assurance in areas of the laboratory. etc. | 11/12/2019 |
| 13305 | Samdi Tech Chicago, IL Research Assistant (Full-time) BS in biology, biochemistry, chemistry or related Exp: 0-3 years |
The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include supporting the preparation of reagents and materials for running biochemical assays, assisting in executing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, integrating automated liquid handling, and supporting fundamental laboratory functions. | 11/12/2019 |
| 13306 | Samdi Tech Chicago, IL Research Associate- Biochemical Assay Specialist (Full-time) MS in biology, biochemistry, chemistry or related Exp: 1+ year(s) |
The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include handling and processing of reagents and materials for running biochemical assays, designing and performing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, take a project leadership role on multiple targets/enzymes, integrating automated liquid handling, and writing and maintaining Standard Operating Protocols (SOPs). | 11/12/2019 |
| 13307 | Rho Durham, NC Quality Assurance Associate BS/BA Exp: 1-2 year(s) |
The Quality Assurance Associate will assist the Quality Assurance team in day-to-day operations of Quality Assurance activities as it relates to Rho’s audit, internal support and quality management system activities. This position will perform a variety of administrative duties in support of the QA efforts, including reviewing, maintaining and filing of documents, scheduling meetings, and working with project teams and databases. This position also will have primary oversight of the Rho QA Files and filing system, will provide support during sponsor audits, will be involved in the Rho vendor qualification program, and may assist with auditing activities under the oversight of a Rho QA Auditor or Service Leader. etc. | 11/12/2019 |
| 13308 | Rho Durham, NC Clinical Systems Associate BS/BA Exp: 1-2 year(s) |
The Clinical Systems Associate will assist Rho’s clinical systems and process team members in day-to-day operations including administration of our clinical trial management system (CTMS) and electronic trial master file system (eTMF). This team member will work closely across system teams to enter clinical metadata, ensure data quality and accuracy, identify and escalate issues, suggest solutions, respond to internal customers, and help to support system configurations. The position will offer the opportunity to learn about all aspects of clinical research support, including processes across functional areas, best practices and process standards, and the CTMS and eTMF software applications. etc. | 11/12/2019 |
| 13309 | ProSciento San Diego, CA PT Pharmacy Technician HS diploma or equivalent Exp: 1 year |
This position is responsible for performing pharmaceutical related functions in compliance with state and federal regulations, protocol specific requirements, and the Company’s values, policies, and procedures under the direction of the Pharmaceutical Services Supervisor. Essential Duties and Responsibilities include the following. Other duties may be assigned at the company’s sole discretion. Receive, label, store, organize, and return/destroy study medications for clinical trials. Prepare and update all drug inventory logs and ensure logs are current with all clinical trial drug preparation schedules. etc. | 11/12/2019 |
| 13310 | Rakuten Medical San Diego, CA Associate, Technical Operations (Downstream) BS/BA Exp: 1+ year(s) |
The Associate in Downstream Purification and Conjugation is a key member of the Technical Operations team and will be involved in supporting Rakuten Medical’s research and discovery programs and CMC activities. Candidate responsibilities include performing routine purification and conjugations, testing of research-grade proteins and in-process testing of process development samples, and assisting in developing and implementing scalable new methods and technologies to enhance product-specific and process-specific purification/conjugation methods for protein/PIT programs. etc. | 11/12/2019 |
| 13311 | Rakuten Medical San Diego, CA Senior Technical Associate/Technical Associate, Molecular Biology MS Exp: 0-3 years |
Key Duties and Responsibilities: Conducting primer design, PCR, gel electrophoresis, Quikchange mutagenesis, restriction enzyme digestion/analysis, ligation, sequence and ligation independent cloning. Responsible for cloning constructs (antibody, therapeutic proteins, or research reagents) and purifying DNA at different production scales (Mini-, Midi-, Maxi-, Giga-) to support critical reagents needs, material generation efforts, and cell-line development activities. Responsible for ordering and maintaining raw materials, lab supplies, and providing oversight to inventory of all required working reagents. Maintain, calibrate, and troubleshoot molecular biology-related equipment. etc. | 11/12/2019 |
| 13312 | Icon PLC North Wales, PA CTA BS/BA in life sciences Exp: Entry Level |
This unique opportunity is designed for individuals with a Bachelor's Degree in Life Sciences, strong organizational skills, excellent written and verbal communication, and working knowledge of computer systems including Microsoft Word, Excel, Outlook, and PowerPoint. ICON, a leading Clinical Research Organization, is seeking passionate, resilient and inspiring Graduates to join our team as a Clinical Trial Assistant. This opportunity offers an entry-level permanent position to highly skilled individuals interested in a career in clinical research. | 11/11/2019 |
| 13313 | Icon PLC Portland, OR Laboratory Assistant (Maintenance Tech) BS/BA Exp: 1 year in operations/sciences/equipment |
The Lab Assistant (Maintenance Technician) supports the activities of Production, Development, and the Clinical Laboratories. The Maintenance Technician performs equipment maintenance and cleaning, qualification, assists in the development of equipment specifications and other equipment or facility related activities to ensure proper qualification, function and reliability. | 11/11/2019 |
| 13314 | Helmer Scientific Noblesville, IN Manufacturing Trainee HS Diploma/GED Exp: None |
Performs repetitive assembly/fabrication/materials tasks using basic hand tools to build either parts for or actual temperature-controlled storage units, refrigerators/freezers and thawing systems, Cleans and packs units, handles material for distribution. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. Ensure that device history records are completed according to FDA GMP requirements. Complete nonconformance records according to established procedures and GMP requirements. | 11/10/2019 |
| 13315 | Helmer Scientific Noblesville, IN Assembler I* HS Diploma/GED Exp: 1-3 years in general assembly |
The Assembler I: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. Performs repetitive assembly task using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems. May be assigned to clean and pack units. | 11/10/2019 |
| 13316 | Helmer Scientific Noblesville, IN Assembler I - Clean & Pack* HS Diploma/GED Exp: 1-3 years in general assembly |
Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. | 11/10/2019 |
| 13317 | High Point Clinical Trials Center High Point, NC Lab Supervisor CLS/MT Associates, BS, BA Exp: 1 year lab experience |
This position ensures the full reconciliation of all specimens submitted to outside client and vendors in a manner fully compliant to Good Clinical Practice under FDA guidelines. Completes all study procedures as per FDA regulations, GCP guidelines and protocol requirements. Assists with and performs laboratory procedures including sample check-in, preparation, centrifugation, storage and shipment. Applicants should have demonstrated team management skills as well as working knowledge of IATA sample shipment processes, CLIA-waivered laboratory processes, and ability to fully manage external vendors for our clinical trial testing needs. | 11/10/2019 |
| 13318 | High Point Clinical Trials Center High Point, NC Research Nurse NC nursing license Exp: 1 year practical nursing experience |
Assist in conduct of clinical studies. Provides licensed nursing coverage for studies and performs procedures as allowed by training and delegation. Assist in the conduct of clinical studies while providing licensed coverage. Performs all job responsibilities in accordance with standards of Good Clinical Practice (GCP), clinic standard operating procedures (SOP’s), and OSHA guidelines. Perform tasks such as EKG’s, vital signs, phlebotomy, insertion and maintenance of IV catheters. | 11/10/2019 |
| 13319 | Hikma Cherry Hill, NJ Quality Lab Associate I, Env. Monitoring BS/BA Degree in Microbiology or Biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. Document EM testing into the EM database prior to incubation, ensure samples are correctly incubated, and record sample results in the EM database following incubation. Audit personnel aseptic technique in controlled areas including during process simulations (media fills). Document test data clearly and accurately. Maintain data integrity and ensure compliance with company policies, procedures, cGMPs, and regulatory requirements. | 11/10/2019 |
| 13320 | Hikma Columbus , OH Technician II, Chemstore 2nd Shift HS Diploma/GED Exp: Entry LEvel |
Performs the set of tasks referred to as “window work” within the Chemstore while collecting, washing, and redistributing laboratory glassware. Escalates any washer issues discovered to the GMP department and communicates shortages/inventory needs to their Manager. | 11/10/2019 |
| 13321 | Hillrom Alexandria, LA Field Service Technician I HS Diploma/GED Exp: 0-2 years in FDA related industry/customer service |
The primary duties of a Medical Equipment Service Representative involve client facing customer service and minor medical equipment repairs. Responsible for the pick-up and delivery of medical equipment, using a company provided vehicle to customer facilities. Periodically work on an on-call rotation that involves a 24/7/365 operation. Responsible for direct customer contact | 11/10/2019 |
| 13322 | Hillrom Albuquerque, NM Field Service Technician I HS Diploma/GED Exp: 0-2 years in FDA related industry/customer service |
The primary duties of a Medical Equipment Service Representative involve client facing customer service and minor medical equipment repairs. Responsible for the pick-up and delivery of medical equipment, using a company provided vehicle to customer facilities. Periodically work on an on-call rotation that involves a 24/7/365 operation. Responsible for direct customer contact | 11/10/2019 |
| 13323 | Hillrom Batesville, IN Engineer I R&D - Embedded Software BS/BA in computer science/engineering Exp: 0-2 years in engineering/technical role |
As an Embedded Software Engineer, you will develop innovative medical software in a fast-paced environment. The ideal candidate will have a passion for bringing cool ideas to life and maximizing hardware and software performance. You will be responsible for writing firmware for device drivers, task manager, device manger, control algorithms, and various communication protocols which make our products exceptional. You develop tools which automate the software build process, system design and production testing. | 11/10/2019 |
| 13324 | Homology Bedford, MA Research Associate, Analytical Development (6 Month Contract) BS/BA in biological sciences Exp: 0-2 years in biochemical/biological analyses |
The role of Analytical Development Research Associate is to aid in developing and refining analytical methods to characterize AAV vector products. The individual in this role will be a highly-skilled, talented and motivated researcher who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. The candidate will participate in the comparison of AAV vector products produced internally with those produced externally as well as the optimization and qualification of molecular and bioanalytical assays such as HPLC and capillary electrophoresis. | 11/10/2019 |
| 13325 | Hovione East Windsor, NJ Process Technician - Drug Product Continuous Manufacturing BS in engineering Exp: 1-2 years in chemical/pharma operations |
The Process Technician will support the installation and qualification of a GMP continuous tablet manufacturing line, highly automated, with Process Analytical Technology enabled control. This position will also support the development and manufacturing activities for drug product and formulation development projects. | 11/10/2019 |
| 13326 | Hovione East Windsor, NJ Process Engineer BS in chemistry/chemical engineering Exp: 1-3 years in chemical/pharma operations |
The Process Engineer will ensure that the use of the best process engineering knowledge will be applied in scaling up chemical and spray drying projects to maximize customer satisfaction and Hovione’s interests and in compliance with all Federal, State, Local and internal policies. Plan and design manufacturing processes based on chemical procedures to run safely and effectively in a pilot plant/kilo lab in accordance with the best known practices ensuring cGMP compliance. Contributes to the Process Hazard Analysis (PHA) of all processes under his/her responsibility and assures that all identified hazards are addressed prior to performing any activities within operations. | 11/10/2019 |
| 13327 | iCAD San Jose, CA Mechanical Engineer - R&D BS in Mechanical Engineering, or closely related Exp: 1- 5 years |
Fundamental understanding of Mechanical Design and Engineering. Product design experience in plastics, ceramics and/or metals. Fixture design for assembly and inspection. Lead experimental builds related to the development of the product. Run validation protocols related to design and production. | 11/10/2019 |
| 13328 | Icon PLC Farmingdale, NY Laboratory Study Start-Up Specialist BS Exp: 1 year in clinical trials |
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/10/2019 |
| 13329 | Icon PLC Lexington, KY DPC Assistant HS Diploma/GED Exp: 1 year in medical office/admin |
The DPC Assistant will provide support services (logistical, technical and administrative) to the Direct to Patient Contact (DPC) project team all along the project, while complying with the deadlines, budgets, quality and regulatory requirements defined for each project. For each project, the Direct to Patient Contact Manager (DPCA) works under the technical and functional supervision of the dedicated Direct to Patient Contact Manager (DPCM). | 11/10/2019 |
| 13330 | Icon PLC Brentwood, TN CTA BS/BA in life sciences Exp: Entry Level |
This unique opportunity is designed for individuals with a Bachelor's Degree in Life Sciences, strong organizational skills, excellent written and verbal communication, and working knowledge of computer systems including Microsoft Word, Excel, Outlook, and PowerPoint. ICON, a leading Clinical Research Organization, is seeking passionate, resilient and inspiring Graduates to join our team as a Clinical Trial Assistant. This opportunity offers an entry-level permanent position to highly skilled individuals interested in a career in clinical research. | 11/10/2019 |
| 13331 | Icon PLC Raleigh, NC Client Services Assoc II, PCS BS/BA Exp: 1-2 years in clinical research |
As a Client Services Associate II, you will be responsible for supporting efforts to maintain and expand upon client relationships for the assigned PCS service area(s) through costing and proposal development, single service project planning and support, and client communication management. Support clinical research projects in the areas of scale management, translations, printing and distribution, and technology implementation. | 11/10/2019 |
| 13332 | Icon PLC North Wales, PA Configuration & QC Spec I BS Exp: 1 year in clinical research |
Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/10/2019 |
| 13333 | Helmer Scientific Noblesville, IN Customer Service Rep HS Diploma/GED Exp: 0-3 years in call center/customer service |
The Customer Service Reprentative: Provides domestic and international customer support via telephone, fax and e-mail to our internal and external customers. Support includes product and part support, order entry, CRM data entry, coordination of shipping requirements and varying degrees of assistance to customers. | 11/10/2019 |
| 13334 | Homology Bedford, MA Research Associate/ Sr. Research Associate, Upstream Fermentation MS in molecular biology, biochemistry, or related Exp: 0-2 years |
Homology Medicines seeks an outstanding Research or Senior Research Associate in the Upstream Process Development team to assist in the development of plasmid manufacturing processes and scale-up strategies. The individual in this role will be a highly-skilled, talented and motivated researcher who will focus on the scale up of bacterial methods for producing DNA plasmids. | 11/10/2019 |
| 13335 | Hikma Cherry Hill, NJ Chemical Process Operator I BS in chemistry or related Exp: 1 year in pharma, batch processing, or lab experience |
Using company procedures and guidelines, the Chemical Process Operator I is responsible for a limited spectrum of duties within the department. This may include but is not restricted to: weighing, mixing, equipment cleaning, tank cleaning, tank movement and PM activities, etc. | 11/10/2019 |
| 13336 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro BS in microbiology/biology Exp: 0-2 years pharma microbiology experience |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management. Use sophisticated laboratory instruments and computer systems to collect and record data. Perform advanced laboratory assays requiring precise analytical and aseptic technique skills. | 11/10/2019 |
| 13337 | Hikma Columbus , OH Technician 1, Manufacturing Flow 3&4, 2nd Shift HS Diploma/GED Exp: Entry LEvel |
Sets up, runs and cleans equipment in moderately complex production areas (Dispensing, Charging and Bin Washing in Flows 1-6 or Dispensing or Layering in Flow 7) and makes product following appropriate procedures in a clean and safe work environment meeting with all cGMP, FDA, DEA, OSHA and other applicable regulations (see appendix for specific details). Performs the Setup, Run and Clean of Dispensed, Manufactured and Packaged product ensuring compliance with and following all appropriate policies, procedures, formula cards, batch records, etc., cGMP, FDA, DEA OSHA and other applicable regulations. | 11/10/2019 |
| 13338 | GBT South San Francisco, CA CONTRACT - CLINICAL TRIALS ASSISTANT BS/BA or equivalent Exp: Experience preferred but not required |
The Clinical Trials Assistant (CTA) is responsible for providing support to the lead Clinical Trial Manager and the study execution team, clinical tracking and document maintenance as applicable to study vendors and clinical trial sites. The CTA will work closely with a cross-functional team to ensure that clinical trials are conducted in a timely fashion and in compliance with GBT SOPs, ICH/GCP/regulatory guidelines, company goals, and budgets. | 11/9/2019 |
| 13339 | Global Pharma Tek Edison , NJ Clinical Project Assitant BS in pharmacy, health care, or related Exp: 1-2 years |
Responsible for strategic and operational activities of clinical research studies in blood cancer metabolism to ensure adherence to intended timelines and achievements of study goals, while ensuring quality by FDA, EMEA, ICH and GCP guidelines. Facilitating interdisciplinary activities, participating in the clinical trial working group (CTWG), Site Management Team (SMT), and internal team meetings to meet the goals and established timelines | 11/9/2019 |
| 13340 | Global Pharma Tek Edison , NJ Equipment Validation Engineer BS in mechanical/industrial engineering Exp: 1-2 years |
Develop, Implement and Install filter integrity testing methods to available automated Filter Integrity Testers (FITs) available on site to verify the integral of the vent filters that will used in the process for WFI Tanks, Autoclaves, supply clean compressed air and as required. Prepare protocols and reports for Validation Project Plan, Validation Master Plan, IQ, OQ, OQ, Traceability Matrix, Engineering test Plans, and Commissioning test strategies following the site Good Data and Documentation Practices (GDP) during protocol execution for qualifying the system or facility | 11/9/2019 |
| 13341 | Global Pharma Tek Edison , NJ Regulatory Affairs II BS in pharma sciences or related Exp: 1-2 years |
Managing and delivering regulatory submissions to global health authorities required to support the maintenance, development and registration of products and performing the following required activities depending on the particular project and assigned submission(s). Establishing Dossier Plans for the assigned Global submission types as needed to support the lifecycle of one or more products in generating dossier plans that will reflect inputs from functional area representatives and key stakeholders; | 11/9/2019 |
| 13342 | Global Pharma Tek Edison , NJ Lab Equipment Qualification Engineer BS/BA in pharmacy or chemistry Exp: 1-2 years |
Execute Validation and Qualification protocols which include installing, operating and maintaining of GMP Lab Equipment and Instruments (HPLC, UV-Vis Spectrometers, FTIR, GC, pH meters, Conductivity meters, Analyzers etc.) and manufacturing equipment like sterilizers and autoclaves to confirm if the instrument is compatible and compliant with Manufacturing, analysis, Company and FDA regulations. Perform validation and qualification documents include User requirement specifications, functional requirement specifications, Installation Qualifications (IQ), Operational Qualifications (OQ), Performance Qualifications (PQ), Validation summary reports, Change Control etc. for various lab instruments utilized by Quality control and Quality assurance teams; | 11/9/2019 |
| 13343 | Global Pharma Tek Edison , NJ Associate Operations Specialist BS/BA in pharmacy or pharmacology Exp: 1-2 years |
Review, assess and process Lifecycle Safety data and information, across all service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Perform data entry for tracking and safety database, coding relevant medical terminology, writing, descript narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations and ensuring reports are sent to the customer within assigned deadlines. | 11/9/2019 |
| 13344 | Global Pharma Tek Edison , NJ Submission Specialist - Regulatory Affairs BS in regulatory affiars/health admin Exp: 1-2 years |
Performing hands-on daily submission compilation and publishing activities associated with preparation of various dossier types and safety reports, for both new product marketing applications and/or marketed product maintenance packages. Performing overall quality of the assigned documents and dossiers which must comply with all internal Bayer best practices, meet global regulatory requirements, and facilitate the review and timely approval by appropriate regulatory authorities. Supporting the compilation of global dossiers and to deliver technically compliant submission documents/reports, which contribute to the development of submissions that meet the technical requirements and standards set by relevant health authorities. | 11/9/2019 |
| 13345 | Global Pharma Tek Edison , NJ Specialist Study Management BS in regulatory affiars/health admin Exp: 1-2 years |
Review and process start up documents, including Sub Investigator’s documents in compliance with ICH-GCP, and client’s Procedural Documents; Assist SATS with obtaining and maintaining essential documents in compliance with ICH-GCP, and client’s Procedural Documents; Attend weekly study team meetings and be prepared to provide a report on vendor spreadsheet status and sub I document status; Create and/or import clinical-regulatory documents into the A New Global Electronic Library (ANGEL) according to the Global Document List (GDL) ensuring compliance with the client’s Authoring Guide for Regulatory Documents to support publishing in ANGEL; | 11/9/2019 |
| 13346 | Goodwin Biotechnology Plantation, FL Upstream Manufacturing Technician HS Diploma or AS in biological/physical sciences Exp: Entry Level |
Assists Upstream Manufacturing and Cell Culture Operations with Manufacturing in accordance with Master Batch Records and in compliance with GMP regulations and guidelines. Monitors Manufacturing Processes, Operates Analytical Laboratory Equipment and provides Operational Support for USP-MFG activities. Compiles electronic /laboratory notebooks, maintains laboratory equipment, and equipment logs and monitors supplies. | 11/9/2019 |
| 13347 | Goodwin Biotechnology Plantation, FL Upstream Manufacturing Technician BS in biological/physical sciences Exp: 1-2 years in cell culture |
Responsible for the execution of a Manufacturing Batch Records (MBR) for specific projects to manufacture cell derived biopharmaceuticals in compliance with cGMP guidelines and regulations. Activities include cell culture in various cell culture vessels including preparation of inocula for bioreactor production, and operation of various bioreactors. Assists in all Upstream Development/Manufacturing activities including; cell culture, cell banking, media optimization, seed train design, feed strategy, bioreactor parameter optimization, harvest clarification, and technology transfer to manufacturing. | 11/9/2019 |
| 13348 | Gore Elkton, MD R&D Technician BS in chemical/sciences/engineering Exp: 1-3 years |
W.L. Gore & Associates Inc. is seeking an associate to join the R&D Technician Lab Team at one of the Fabrics Division’s facilities in Elkton, Maryland. The primary focus of this commitment is to support projects and hands on testing needs for our Durable Water Repellent coating on laminates. Performing lab functions accurately and efficiently, including but not be limited to: Hands on testing, sample preparation, and test method development. Writing and implementing procedures.Operating and maintaining analytical equipment | 11/9/2019 |
| 13349 | Gore Flagstaff, AZ Electrical Automation Design Engineer BS in engineering Exp: 1 or more year (can be coop/internships) |
In this role, you will be involved in software design, electrical design, specification, installation, startup, validation, project management, and support for new and existing equipment and systems. Performing electrical design and hands-on support for process equipment (e.g., drives, programmable logic controller [PLC] logic programming, human-machine interfaces [HMIs], wiring schematics, power systems, instrumentation, and motor control systems). Being an integral member of a project team that specifies, constructs, commissions and validates new manufacturing equipment | 11/9/2019 |
| 13350 | Gradalis Carrollton, TX Clinical Research Assistant BS in life/health sciences Exp: 1 or more years |
The Clinical Research Assistant coordinates the research and administrative activities of clinical trials for Gradalis. The Clinical Research Assistant works for the Clinical Operations Manager to provide support in compliance with the FDA Code of Federal Regulations (CFR), the ICH Good Clinical Practice (GCP) Guidelines, OHRP/DHHS guidelines and Gradalis Standard Operating Procedures. | 11/9/2019 |
| 13351 | Grail Menlo Park, CA Research Associate 2 - R&D Technology Development MS in molecular biology, biochemistry, or related Exp: 1 year or more |
GRAIL is seeking a Research Associate for the R&D technology development team to contribute to the development and optimization of assays for early cancer detection. The successful candidate will be responsible for planning and execution of experiments and data analysis with the guidance of senior scientists. Develop experiment plans to support study objectives. Ensure laboratory activities are performed in compliance with best practices for assay and instrument operation, safety, and result documentation | 11/9/2019 |
| 13352 | Grail Menlo Park, CA Equipment Engineering Technician BS/BA in engineering or sciences Exp: 0-2 years in lab |
As an Equipment Engineering Technician, you are responsible for supporting laboratory equipment management procedures, in alignment to our internal Quality Management System, to ensure better performance within Laboratory Operations. This will include global laboratory equipment support, sustainment, and operations activities across Production/Clinical, Product Development, Research and Development laboratories, in accordance with CLIA/CAP, FDA, cGMP and/or GLP guidelines. | 11/9/2019 |
| 13353 | Grail Menlo Park, CA Clinical Lab Associate I BS/BA in Biomedical Laboratory Science, Clinical Science or related field preferred. Exp: 1-2 years |
The Clinical Laboratory Associate (CLA) is responsible for assisting the Clinical Laboratory Scientist and supporting the daily operations of the Clinical Laboratory. CLA may serve as a team lead to the CLA team to coordinate tasks, divide workload, manage projects and review documents as assigned. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask, be flexible with tasks and schedules and ability to work independently in a team environment. | 11/9/2019 |
| 13354 | Grand River Grand Rapids, MI ASEPTIC MANUFACTURING ASSOCIATE - 3RD SHIFT HS Diploma/GED Exp: 0-1 years in manufacturing or lab work |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. Follow production and manufacturing procedures. Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed. Train in various manufacturing tasks including, but not limited to: fill/finish, formulation, lyophilization, sanitization, component and equipment preparation, and finished product inspection and packaging activities. | 11/9/2019 |
| 13355 | GreenLight Biosciences RTP, NC Research Technician Formulations BS in pharma sciences, or chemistry Exp: 0-2 years in lab |
GreenLight Biosciences is seeking for a Formulation Laboratory Technician to be part of the Formulation team to work on the design of new formulations under the guidance of a formulation scientist as well as the improvement of existing formulations and provide support to the manufacturing operations. The technician will be responsible for evaluating formulations, troubleshooting production when necessary and sample preparation. Strong technical, organizational and communication skills are essential. Applicant must be a team player able to function in a highly collaborative and fast-paced environment. | 11/9/2019 |
| 13356 | Grifols San Diego, CA Research Associate 2 BS/BA or MS Exp: 1-3 years |
Research Associate 2 is responsible for designing and performing experiments while collaborating and communicating effectively. Performs moderately complex experiments with input from supervisor. Able to summarize related groups of experiments. Provides input to the experimental design. Is able to analyze experimental data with minimal input from supervisor. Interprets experimental results in context of overall experimental goal. | 11/9/2019 |
| 13357 | Grifols Clayton, NC Associate Chemist-QC AS/AA or BS/BA Exp: 0-2 years with chemistry courses for degrees |
Performs chemical testing of moderate to advanced complexity within a Quality Operations Laboratory in a safe, accurate, and efficient manner following established written procedures while maintaining complete and accurate records of the work and results. This testing is required for the release of raw materials, in-process materials, and final containers. Conducts various routine and non-routine chemical testing (assays) according to procedure. Learns and follows the methods and the techniques of the chemical tests to be performed. This learning is a continuation of learning that occurred as Assistant Chemist. | 11/9/2019 |
| 13358 | Grifols Savannah, GA Phlebotomist HS Diploma/GED Exp: 0-1 years |
You assist in determining the suitability of donors to undergo plasmapheresis prior to venipuncture. You establish rapport with donors to ensure overall customer happiness with the center to support long-term donation, all while ensuring donor confidentiality. Sets up, disconnects, and operates the automated plasmapheresis machines including response and evaluation of all autopheresis troubleshooting displays, documentation of exceptions, etc. Ensures the proper calibration and maintenance of autopheresis machines and associated equipment. May be trained to repair plasma equipment. Disconnects and disposes of all contaminated disposable equipment. Ensures proper cleaning of equipment and work area between donors. Maintains accurate and thorough documentation of production records. | 11/9/2019 |
| 13359 | Grifols Ocala, FL Biomedical Technician HS Diploma/GED Exp: 6-12 months as medical assistant or phlebotomy training |
Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Responsible for preparing donors for plasmapheresis procedure. Review donor record files for accuracy and completeness. Collect plasma by setting up the autopheresis instrument, performing the venipuncture and utilizing an Automated Plasmapharesis machine. Evaluate vein performance by checking data with known norms to identify possible problems; make corrections in order to expedite donation time and ensure product quality. Conducts all phlebotomies in compliance with all federal, state, and Biotest regulations. | 11/9/2019 |
| 13360 | Grifols Rock Hill, SC Biomedical Technician HS Diploma/GED Exp: 6-12 months as medical assistant or phlebotomy training |
Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Responsible for preparing donors for plasmapheresis procedure. Review donor record files for accuracy and completeness. Collect plasma by setting up the autopheresis instrument, performing the venipuncture and utilizing an Automated Plasmapharesis machine. Evaluate vein performance by checking data with known norms to identify possible problems; make corrections in order to expedite donation time and ensure product quality. Conducts all phlebotomies in compliance with all federal, state, and Biotest regulations. | 11/9/2019 |
| 13361 | Grifols Clarkville, TN Quality Associate HS Diploma/GED Exp: 0 years |
Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual. Participate in the Quality Assurance meetings and be part of the Quality Assurance team. Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Perform weekly review of equipment incident logs. | 11/9/2019 |
| 13362 | Grifols Moorhead, MN Phlebotomist HS Diploma/GED Exp: 0-1 years |
You assist in determining the suitability of donors to undergo plasmapheresis prior to venipuncture. You establish rapport with donors to ensure overall customer happiness with the center to support long-term donation, all while ensuring donor confidentiality. Sets up, disconnects, and operates the automated plasmapheresis machines including response and evaluation of all autopheresis troubleshooting displays, documentation of exceptions, etc. Ensures the proper calibration and maintenance of autopheresis machines and associated equipment. May be trained to repair plasma equipment. Disconnects and disposes of all contaminated disposable equipment. Ensures proper cleaning of equipment and work area between donors. Maintains accurate and thorough documentation of production records. | 11/9/2019 |
| 13363 | Gritsone Pleasanton, CA MANUFACTURING ASSOCIATE I/II, DOWNSTREAM BS in biological/physical sciences Exp: 0-2 years in cGMP manufacturing |
The Manufacturing Associate will execute activities associated with purification manufacturing in a clean room environment. This role will also need to assist with cell culture, aseptic fill, and buffer prep processes as well as maintain material inventory in labs. Possess experience in purification activities including but not limited to tangential flow filtration, anion exchange chromatography, and diafiltration. Responsible for day to day manufacturing activities including stocking of materials, preparation of documentation, cleaning and sanitization of rooms and equipment, operation of process equipment. | 11/9/2019 |
| 13364 | Guardant Redwood City, CA Clinical Trials Assistant BS/BA in biological sciences Exp: 1 year in clinical research |
The Clinical Trial Assistant (CTA) is primarily responsible for the coordination of activities associated with the setup and management of clinical studies under the direction of, or as delegated by a member of the Clinical Trial team. Responsibilities will range from clinical study coordination to data entry projects and general office work. | 11/9/2019 |
| 13365 | Guardant Redwood City, CA Reporting Assistant II AS/AA or BS/BA in lab/clinical sciences Exp: 1 year of lab experience |
The Reporting Assistant (RA)II is responsible for assisting the reporting Clinical Laboratory Scientists (CLS) and supporting the daily operations of the post-analytical reporting process.The RA IIis responsible for preparing all preliminary reports, labeling folders, documenting controls for CLS review and assisting sample status in the Clinical Laboratory. | 11/9/2019 |
| 13366 | Guardant Redwood City, CA Client Services Associate BS/BA Exp: 1 year in client services |
We are looking for a full-time Client Services Associate (CSA). The CSA is responsible for providing exceptional support to Guardant Health customers, the Guardant Health Clinical Laboratory, Sales Representatives, and our billing partners. CSA is responsible for receiving and responding to all types of communication: phone, email and web inquiries from customers (physician offices, laboratories, and hospitals), sales representatives and patients. | 11/9/2019 |
| 13367 | Harpoon Therapeutics South San Francisco, CA Clinical Research Associate BS/BA in science/health care Exp: 1-2 years in drug development |
The Clinical Research Associate is a key member of the team responsible for planning, successful implementation and management of one or multiple clinical trial(s). Responsibilities include assisting in the development of study protocols, case report forms, clinical reports, performing site monitoring visits, and interfacing with site coordinators, field clinical staff, CROs and other company representatives. High level relationships across all functional areas that interact with Clinical Operations (including Product Development, Research, Translational Medicine, etc.) will also be required. | 11/9/2019 |
| 13368 | HealPros Atlanta, GA IT Support Technician HS Diploma or higher Exp: 6-24 months of electornics work |
We have an immediate opening for an IT Support Technician to be based out of our corporate office in Buckhead, GA. This is a full-time position and will be responsible for managing HealPros's equipment in our facility or at the location of our technologists. Under the supervision of the IT Administrator, the IT Support Technician will perform troubleshooting techniques to resolve equipment issues and maintain it in good working order. | 11/9/2019 |
| 13369 | Health Decisions Durham, NC Business Development Associate (Inside Sales) BS/BA Exp: 1 year in sales |
We are seeking a Business Development Associate who will be responsible for lead generation by proactively prospecting and qualifying targeted leads by telephone and email. The ideal candidate will be highly skilled in fostering relationships with the goal of converting leads to new sales opportunities. Initate initial client engagement, including ensuring client-readiness of materials for client meetings including briefing documents and call presentation development; develops call agenda and hosts prep sessions with internal teams in advance of client engagement . | 11/9/2019 |
| 13370 | Helix San Diego, CA Research Associate BS in Biology, Genetics, Chemistry, Biochemistry or related Exp: 1-3 years laboratory experience |
As an RA in the Helix R&D group, you will work in a dynamic and fast-paced environment to develop robust, scalable genetic testing processes to be used in cutting-edge clinical genetics applications. Execute Next Generation Sequencing methodologies and laboratory processes. Participate in validation of test methods for existing and new products for the clinical lab. Operate Next Generation Sequencing methodologies at R&D and production scale | 11/9/2019 |
| 13371 | Cambrex Whippany, NJ Specialist Batch Disposition BS/BA Exp: 1-5 years in pharma product record review |
The Specialist Batch Disposition is responsible for review of proposed Master Manufacturing/Packaging batch records; issuing batch records to the production floor; review of executed batch records and product release. Review batch records, protocols, and reports for accuracy, completeness and to identify any potential issues. Maintain/control hardcopy files for all effective master batch records. Create/revise/maintain PDF versions of all master batch records. | 11/9/2019 |
| 13372 | H3 Biomedicine Cambridge, MA Research Assistant Tumor Immunology & Neoantigens BS or MS in pharmacology, animal science, oncology, immunology, or related Exp: 1-2 years industry experience |
The successful candidate will conduct rodent in vivo studies utilizing a wide range of technical procedures. Experience performing mouse studies, a strong work ethic, and the ability to be a collaborative team member are essential. Perform mouse in vivo studies to advance our lead research and development programs. Conduct dosing (iv, oral gavage), blood sampling, tissue harvesting, and data recording. Perform sample analysis using defined molecular and biochemical assays | 11/9/2019 |
| 13373 | Harpoon Therapeutics South San Francisco, CA Clinical Trial Assistant BS/BA in biological/health sciences Exp: 1 year in clinical research |
We are seeking a highly motivated CTA to be responsible for the coordination of activities (primarily administrative tasks) associated with Clinical Trial startup and maintenance under the direction of, or as delegated by a member of the Clinical Trial team. Responsibilities will range from clinical study coordination to data entry projects and general office work. | 11/9/2019 |
| 13374 | Pfizer St. Louis, MO Associate Scientist, Cell Line Development BS in cellular/molecular biology or related Exp: 0-3 years |
A technical, lab-based position is available within Pfizer’s Cell Line Development (CLD) organization. The position will be primarily involved in mammalian CLD portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer’s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. The successful candidate will possess excellent aseptic technique and have experience with mammalian cell culture and recombinant protein expression. etc. | 11/5/2019 |
| 13375 | Pfizer Andover, MA Associate Scientist, Cell Line Development BS in cellular/molecular biology or related Exp: 0-3 years |
A technical, lab-based position is available within Pfizer’s Cell Line Development (CLD) organization. The position will be primarily involved in mammalian CLD portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer’s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. etc. | 11/5/2019 |
| 13376 | Pfizer Groton, CT Technical Associate, Comparative Medicine HS diploma to BA/BS Exp: 1 year |
The Technical Associate’s primary responsibility is to provide basic husbandry, handling, restraint and health surveillance of laboratory animals in compliance with local regulatory requirements. This individual will also provide daily record keeping of common laboratory species, their environments, and provide basic technical assistance (i.e., restraint, injections, bleeds) to other technicians and researchers. Other more specialized functions, depending on interest and aptitude may be assigned in the areas of technical and research services. etc. | 11/5/2019 |
| 13377 | Pfizer Sanford, NC Quality Control Associate Scientist BS/BA in related field Exp: No experience necessary for BS/BA candidates |
This position is an analyst role in the QC Bioanalytical laboratory. Experience with ELISA, PCR, and/or slot blot is preferred. Analyst will be responsible for ensuring the routine testing is scheduled and completed within appropriate timeframes as needed for manufacturing to maintain schedules (STAT testing) or the QA disposition group to disposition batches. Other responsibilities may include, SOP revisions, validation/qualification testing support, etc. etc. | 11/5/2019 |
| 13378 | Pfizer Groton, CT Associate Scientist, Materials Science BS in pharmaceutical science, chemistry, engineering or other related science Exp: 0-2 years |
Pfizer’s Materials Science group is seeking team members with a desire to bring new, cutting edge medicines to patients around the world. The Associate Scientist, Materials Science position is a laboratory-based position with responsibility for investigating and understanding the solid-state chemistry and particle properties of Pfizer’s drug molecules. Responsibilities include generating and interpreting data using state-of-the-art instrumentation and computer models to allow new medicines to be brought to the market. etc. | 11/5/2019 |
| 13379 | PMI Bio. Nashville, TN Chemist I, Analytical Development BS in chemistry, biology or related Exp: 1-2 years |
The Chemist I position, reporting to the Director, Analytical Development, will operate under moderate supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development. etc. | 11/5/2019 |
| 13380 | PMI Bio. Nashville, TN Microbiologist I, Analytical Development BS in biology or related Exp: 0-1 years |
Reporting to the Microbiology Supervisor, the Microbiologist I will be responsible for performing environmental monitoring sampling of ISO class environments and assisting with preparation, characterization, and identification of environmental isolates. He/she will perform raw material and drug product method development and cGMP testing. etc. | 11/5/2019 |
| 13381 | PolarityTE Salt Lake City, UT Research Specialist I BS in biotechnology, engineering, computer science, or related science Exp: 0-2 years |
Under the general supervision of the Director of BME, the Research Specialist I, II or III will support R&D in conducting research projects by contributing to the following: develop protocols for and maintain laboratory equipment; troubleshoot and resolve problems; ensure compliance with lab protocols and safety standards, policies and procedures; performing complex data gathering and analysis. This role serves to assist with conducting pre-clinical research aimed at validating, testing products and discovering, developing innovative medical technologies. etc. | 11/5/2019 |
| 13382 | Portola South San Francisco, CA Clinical Trial Associate unspecified Exp: 1+ year(s) |
The CTA will support the operational management and oversight of aspects of a clinical program. The CTA will participate in the activities associated with the evaluation, initiation, management, and close-out of clinical trials within the Clinical Operations Department. The CTA role provides an outstanding opportunity to work in a cross-functional environment and collaborate with colleagues in Clinical Research, Biometrics, Regulatory & QA, and Program Management. This individual will report into the Sr. Director of Clinical Operations. This is an in-house position. etc. | 11/5/2019 |
| 13383 | Poseida Therapeutics San Diego, CA Research Associate, In Vivo Gene Therapy MS in immunology, molecular biology, or related Exp: 0+ year(s) |
The Research Associate will play a key role in advancing exploratory gene therapy programs that leverage our cutting-edge piggyBac® DNA Modification technology. Responsibilities: Actively participate in our proprietary gene therapy platform technologies to create new human therapeutic candidates. Develop and perform research involving various in vitro and animal laboratory techniques including ELISA, cell/tissue isolations, microscopy, in vivo procedures and animal imaging. Understand and analyze results, and communicate findings in team meetings. Maintain laboratory equipment and facilities, as required. | 11/5/2019 |
| 13384 | Poseida Therapeutics San Diego, CA Temporary Research Technician, Immuno-Oncology BS in immunology, molecular biology or related Exp: 0-3 years |
The Research Technician will support the development of CAR-T cellular therapies against cancer and involve bench work, laboratory studies, and the coordination of research projects with the assistance of a senior lab member and/or the lab director. Please note that this is a temporary position. Responsibilities: Cloning and screening of CAR-T cellular therapies. Studies may include work with molecular biology and cloning techniques, tissue culture of human cell lines, isolation of cells from blood products, virus production, in vitro human cell based immunoassays, and cell separation techniques. | 11/5/2019 |
| 13385 | PPD Richmond, VA Associate Scientist - PCR-Molecular Genomics BA/BS Exp: 1+ year(s) |
As an Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis skills are an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: Problem solving with assistance pertaining to extraction and/or instrumentation problems. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines. etc. | 11/5/2019 |
| 13386 | PPD Richmond, VA Assistant / Associate Scientist - Lab Robotics and Automation BS in biology, chemistry or related laboratory science Exp: 0-2 years |
As an Assistant / Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. etc. | 11/5/2019 |
| 13387 | PPD South San Francisco, CA Associate Scientist / Scientist - Small Molecules, Formulation, TGA, HPLC BS in pharmaceutical chemistry, pharmaceutics or related Exp: 1+ year(s) |
As an Associate Scientist/Scientist, you will work onsite at the client lab facility using state-of-the-art technologies involving preparation and dose analysis of formulations to support toxicology, pharmacokinetic, and other in-vivo studies. You will be responsible for laboratory equipment calibrations and verifications, ordering supplies, as well as designing and conducting Pre-formulation characterization of small molecules. etc. | 11/5/2019 |
| 13388 | PPD Richmond, VA Assistant / Associate Scientist - Cell Culture - Vaccines Sciences BS in biology, chemistry or related laboratory science Exp: 0-2 years |
As an Assistant / Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. etc. | 11/5/2019 |
| 13389 | PPD Middleton, WI Assistant Scientist- HPLC BA/BS Exp: 0-2 years |
As an Assistant Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. etc. | 11/5/2019 |
| 13390 | PPD Richmond, VA Assistant / Associate Scientist - Immunochemistry BS in biology, chemistry or related laboratory science Exp: 0-2 years |
As an Assistant / Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis skills are an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: Problem solving with assistance pertaining to extraction and/or instrumentation problems. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines. Manages QC/QA responsibilities without supervisor or QA input. etc. | 11/5/2019 |
| 13391 | PPD Middleton, WI Assistant Scientist - Physical and Chemical Characterization BA/BS Exp: 0-2 years |
As an Assistant Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. etc. | 11/5/2019 |
| 13392 | PRA Health Sciences Raleigh, NC Associate Clinical Data Coordinator BS/BA Exp: None required |
Supports and leads the clinical data review activities that contribute to delivery of an analyzable database. Responsibilities: Ensures trial deliverables are achieved in terms of timeliness and quality. Reviews clinical and external data for subjects enrolled in clinical research protocols based on edit specifications. Executes data validation programs and reports to facilitate data review. Issues clear, accurate, and concise queries to investigational sites. etc. | 11/5/2019 |
| 13393 | Precision Biosciences Durham, NC Associate Process Engineer, Upstream MS in chemical engineering, biological engineering, or related Exp: 0-2 years |
The Associate Process Engineer, Upstream will work within the Process Development team and will participate in the development of upstream cell culture, delivering best-in-class process design for viral vector drug substances and drug products, for the development of in vivo and ex vivo gene therapies. The candidate will support the process development, process characterization and tech transfer of said processes for GMP manufacturing. The candidate will assist in the clinical progression of in vivo and ex vivo gene therapies by designing and executing process development experiments across a variety of process scales. etc. | 11/5/2019 |
| 13394 | Precision Biosciences Durham, NC Associate Process Engineer, Downstream MS in chemical engineering, biological engineering, or related Exp: 0-2 years |
The Associate Process Engineer, Downstream will work within the Process Development team and will participate in the development of purification processes, delivering best-in-class process design for viral vector drug substances and drug products, for the development of in vivo and ex vivo gene therapies. The candidate will support the process development, process characterization, and tech transfer of said processes for GMP manufacturing. The candidate will assist in the clinical progression of in vivo and ex vivo gene therapies by designing and executing process development experiments across a variety of process scales. etc. | 11/5/2019 |
| 13395 | Poseida Therapeutics San Diego, CA Research Technician, Gene Therapy (Molecular Biology) BS in molecular biology, hematology, virology, or related Exp: 1-3 years |
The Research Technician will play a key role in advancing exploratory gene therapy programs that leverage our cutting-edge piggyBac® DNA Modification technology. Responsibilities: Actively participate in our proprietary gene therapy platform technologies to create new human therapeutic candidates. Develop and perform research involving various molecular and cell biology techniques including nucleic acid development, transfection, cell culture and transgene expression. Analyze data from cell-based assays and report to multidisciplinary groups. Keep current on trends, new products and technologies in the gene therapy and gene editing fields. Maintain laboratory equipment and facilities, as required. etc. | 11/5/2019 |
| 13396 | GSK Lincoln, NE Production Maintenance Technician AS/AA in lectromechanical Technology or Electronic Engineering Technology Exp: 1-3 years in industrial setting |
As Production Maintenance Technician you will be responsible for maintaining, troubleshooting, calibrating and modifying electrical and mechanical systems and equipment and document work on mechanical, electrical, hydraulic, and pneumatic equipment involved in the manufacture and packaging of pharmaceutical products. | 11/3/2019 |
| 13397 | GSK Lincoln, NE Supply Chain – Future Leaders Program BS in business, supply chain, analytics, IT systems, or any sciences/enginnering Exp: 2020 Graduate |
Over three years, our Future Leaders Graduate Program will challenge and support you to grow professionally and personally. You’ll have three stretching rotations within Pharmaceutical or Consumer Healthcare Supply, depending on your area. In both cases, you’ll take on business-critical roles that offer amazing insights into our end-to-end supply chain. You’ll learn about the synergies and challenges that come with delivering optimum value to the business and the customer. | 11/3/2019 |
| 13398 | GSK Lincoln, NE Automation Engineer BS in engineering Exp: 1-3 years |
As an Automation Engineer, you will manage and execute projects related to industrial machine automation for both new and existing equipment. Lead the design and installation of instrumentation and control systems in some of the following areas: building automation systems, data systems, process control, DCS and utility PLC’s which are harmonized with GSK-standards. Provide technical support for existing instrumentation and automation systems. Analyze repairs and maintenance requirements in order to proactively address system weaknesses. | 11/3/2019 |
| 13399 | GSK East Durham, NY Mechanical Engineering – Future Leaders Program, US – 2020 BS in mechanical/manufacturing/biomedical/etc. engineering Exp: 2020 Graduate |
Over three years, our Future Leaders Graduate Program will challenge and support you to grow professionally and personally. You’ll have three stretching rotations in business-critical roles within consumer healthcare supply. Your responsibilities will depend on your engineering discipline, but whatever your specialist area, you’ll get to meet senior leaders and network with other graduates. You’ll also improve your technical skills while gaining valuable leadership expertise. | 11/3/2019 |
| 13400 | GSK Collegeville, PA Reagent Scientist BS ro MS in sciences Exp: 0-3 years |
Development and quality of critical reagents, including characterizing external antibody’s, building isotype-specific antibody reagents, purifying proteins, conducting protein conjugations (e.g. biotin, ruthenium and fluorescent labels), assessing their purity and affinity, and generating certificates of analysis (CofA). Monitor reagents life cycle and characterization to assist with reagent trouble shooting effort. | 11/3/2019 |
| 13401 | GSK Carlisle, PA Packaging Operator- First Shift HS Diploma/GED Exp: 0-1 years in manufacturing |
As a Packaging Operator you will manually assemble, glue, tape and package boxes, cases and other material as needed. Activities also involve set-up, operation, and verification of printing, weighing and robotic equipment as well as staging packaging material, documenting, cleaning, and performing in-process quality checks. The work involves lifting up to 50 lb. containers on a regular basis and moving pallets, totes, and film using a hand truck or similar tools. A thorough understanding of each job function within the work center is essential. | 11/3/2019 |
| 13402 | GSK Rockville, MD Calibration & Instrumentation HS Diploma/GED Exp: 0-1 years cGMP experience |
As Calibration and Instrumentation Staff you will be responsible for supporting the team to ensure manufacturing systems are current on calibration requirements. You will also assist the team with the calibration process system, laboratory equipment, and facilities related utilities. | 11/3/2019 |
| 13403 | Global PharmaTek Edison, NJ Clinical Project Assitant BS in pharmascience,s pharma, health care, etc Exp: 1-2 years |
Responsible for strategic and operational activities of clinical research studies in blood cancer metabolism to ensure adherence to intended timelines and achievements of study goals, while ensuring quality by FDA, EMEA, ICH and GCP guidelines. Providing oversight in clinical research Organization (CRO), Central labs and other external vendors to ensure deliverables are met and methods of communication are developed to facilitate an efficient workflow. Facilitating interdisciplinary activities, participating in the clinical trial working group (CTWG), Site Management Team (SMT), and internal team meetings to meet the goals and established timelines | 11/3/2019 |
| 13404 | Global PharmaTek Edison, NJ Equipment Validation Engineer BS in mechanical/industrial engineering Exp: 1-2 years |
Develop, Implement and Install filter integrity testing methods to available automated Filter Integrity Testers (FITs) available on site to verify the integral of the vent filters that will used in the process for WFI Tanks, Autoclaves, supply clean compressed air and as required. Provide technical support in developing, authoring, and executing the Commissioning, Installation and Qualification protocols for the chromatography skids and other supporting equipment that are used in the production of drug | 11/3/2019 |
| 13405 | Global PharmaTek Irvine, CA Quality Engineer BS in mechanical engineering Exp: 0-2 years |
The Mechanical Engineer, Research & Development will support the Critical Care Mechanical team working on new product designs, technology development and sustaining of core product lines with an emphasis on hands on new product development. | 11/3/2019 |
| 13406 | Freudenberg Jerffersonville, IN Medical Device Assembly / Manufacturing Associate- 1st Shift HS Diploma/GED Exp: 0-2 years |
Hand assemble manufactured components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide suggestions of continuous line/process improvementsHand assemble manufactured components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide suggestions of continuous line/process improvementsHand assemble manufactured components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide suggestions of continuous line/process improvements | 11/2/2019 |
| 13407 | Freudenberg Carpinteria, CA Tool Room Associate HS Diploma/GED Exp: 0-3 years |
Secondary operations and simple machining, including manual machining, grinding, honing, deburring, squaring of stock, and precision material removal to complex specifications with minimal instructions to the requirements of supplied Engineering Documentation. Maintenance of tool room equipment, and of production line molding, extrusion, and assembly equipment are vital functions of the role. Purchasing and stocking of hand tools, metalworking tools, and machining tools. Organization, cleaning, and maintenance of a 5S systematic program for workplace organization in the tool room. | 11/2/2019 |
| 13408 | Frontage Exton, PA Associate Scientist, Bioanalytical Services BS or MS in sciences Exp: Entry level |
Associate Scientist / Bioanalytical Services Essential Functions Provide support for running sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. Coordinate study activities with Responsible Scientist to ensure efficiency and quality. Maintain the proper level of regulatory compliance for each study, helping to address QA audit findings | 11/2/2019 |
| 13409 | Frontage Secaucus, NJ Lab Technician Associates or bachelors in biomedical discipline Exp: 1-3 years in clinical research |
Develop a high level of familiarity and knowledge of the study protocol and flow chart of study procedures. Develop a strategy for implementing study procedures in compliance with study protocols. Performs laboratory procedures (g., preparation for admission testing, safety labs, and processing of biological specimen samples, shipment of samples and documentation of sample processing steps, etc.) as required by study protocol under the supervision of the Clinical Research Coordinator, Principal Investigator, and Sub-Investigators. | 11/2/2019 |
| 13410 | Frontage Exton, PA Associate Scientist-Product Development- CMC MS in pharma sciences, chemistry or biology Exp: 0-4 years |
Perform assigned tasks per procedures compliant with cGMPs and participate in the clinical manufacturing of parenteral, ophthalmic, and other sterile dosage forms. Assist with manufacturing area maintenance such as area monitoring and qualification, purchase of gowning supplies, purchase of equipment and room cleaning supplies, microbiological monitoring supplies. Assist in the equipment set up, operation, maintenance, cleaning as required for the project | 11/2/2019 |
| 13411 | FujiFilm College Station, TX Information Technology – Technical Support I HS Diploma/GED or BS in computer sciences Exp: 1 year in technical support |
Deployment and relocation of desktop systems. Maintenance and repair of desktops, printers and associated peripherals. Supports other IT staff in installing, configuring, testing, maintaining and troubleshooting network, systems hardware and software. Administration of FDBT’s Building Information Management System (BIMS). | 11/2/2019 |
| 13412 | FujiFilm RTP, NC Downstream Production Technician HS Diploma/GED or BS in computer sciences Exp: 1+ year in cGMP production |
Executing Development and Production processes as well as process documentation. Understanding processing principles and scientific theory behind operations steps. Demonstrating proficiency at the advanced skill level. Troubleshooting of equipment/processes. Authoring and routing SOP’s for approval. Assisting in the execution of validation protocols. | 11/2/2019 |
| 13413 | FujiFilm College Station, TX Downstream Manufacturing Technician I AS/AA in biological sciences/engineering, or HS Diploma/GED Exp: HS: 1 year, AA: 0 years |
The Downstream Manufacturing Technician I will work directly with viral purification (either whole particle or split particle), continuous flow centrifuge operation, and sucrose gradient separation, techniques for filtration and chromatographic separation (i.e. column chromatography and HPLC) and viral inactivation. | 11/2/2019 |
| 13414 | FujiFilm College Station, TX Cell Biology Technician BS/BA in biological sciences Exp: 0-2 years |
Writes and revises Standard Operating Procedures (SOPs) and other related Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP) documentation. Manages test samples, reagents and reference standards. Provides QC support for the Sample receipt for Manufacturing. Perform other duties as assigned. | 11/2/2019 |
| 13415 | FujiFilm College Station, TX Calibration Technician II BS or MS in sciences/engineering Exp: 1-2 years in cGMP operations |
Perform calibrations of complex instrumentation on production, laboratory and facility systems ensuring all systems and devices are calibrated in accordance with manufacturer’s specifications and FBDT SOP’s. Assist in the development of investigations resulting from ‘out of tolerance’ conditions with respect to instrumentation. Assist in interfacing with calibration contractors ensuring work is compliant with FBDT SOP’s and cGMP’s to maintain state of the art technology within the facility. Assist in maintaining all calibration records, work orders, and investigations in an orderly and accurate manner in compliance with cGMP’s by the utilization of the site CMMS and Document Management Systems. | 11/2/2019 |
| 13416 | FujiFilm RTP, NC Associate Scientist, Microbial MS or BS Exp: BS: 1+ years, MS: 0 years |
The Upstream Process Development group is seeking an Associate Scientist with experience in microbial technologies. An Associate Scientist assists in conducting experiments for programs. The individual monitors on going experiments and can identify unusual occurrences. An Associate Scientist understands and applies knowledge within area of expertise and can take an active role in non-routine process development activities. | 11/2/2019 |
| 13417 | FujiFilm College Station, TX Associate Scientist – Downstream Process Development MS in chemistry, biology, or life sciences Exp: 1 year experience |
Assist in the development, optimization, and scale-up of chromatography processes (including affinity, IEX, HIC, etc.) and filtration processes (including UF/DF, depth filtration, and sterile filtration, etc.). Operation of chromatographic systems (GE AKTA, and other Unicorn based equipment). Maintaining detailed laboratory notebooks following FDBT procedures. Participate in developing and carrying out experimental protocols. | 11/2/2019 |
| 13418 | Cosette South Plainfield, NJ ASSOCIATE SCIENTIST PRODUCT DEVELOPMENT MS in engineering, or life/pharma sciences Exp: 1-2 years |
he Product Development Scientist will assist the Manager of Product Development in all aspects of new drug product and process development including but limited to – prototype development, lab stability, document creation, process design and optimization, pilot scale-up, assist the process development group in supervising clinical trial manufacturing material, Registration/exhibit batch manufacturing, and process optimization to full scale commercial batch size. Collaborate with all of the Scientific Affair Department (including Process Development, Analytical R&D, Regulatory Affairs, Clinical and Project Management), commercial manufacturing and quality group. | 11/2/2019 |
| 13419 | Cosette South Plainfield, NJ MANUFACTURING OPERATOR 1 - 3rd Shift HS Diploma/GED Exp: 1 or more year as machine operator |
Operate a number of machines used in the manufacturing of pharmaceutical products and have a good working knowledge of elements used in association with batch production, such as equipment cleaning, running filling machines, etc. The operator is responsible for producing acceptable product that meets G&W internal standards, and is also in conformance with GMP and safety standards. 3rd Shift Hours are 11:00 p.m. to 7:00 a.m. | 11/2/2019 |
| 13420 | GenapSys Redwood City, CA Signal Processing Engineer/Data Analyst MS in electrical engineering, physics, math, stats, etc. Exp: 1-4 years in signal processing |
As a Signal Processing Engineer, you would be working in a cross functional R&D team to improve the performance of the core technology through close collaboration with lab scientists, genomic application scientists, and data scientists. You will develop DOE (design of experiments) for troubleshooting and failure mode analysis, extract information from biomedical sensors, develop DNA sequencing base calling algorithms, present written and oral reports and proposals to peers and management, and play an important role in shaping and productionizing new products and cutting-edge applications. | 11/2/2019 |
| 13421 | GeneDx Gaithersburg, MD Microarray Lab Technician BS in medical tech/life sciences Exp: Entry Level |
The Laboratory Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease, using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 11/2/2019 |
| 13422 | GeneDx Gaithersburg, MD Quality Systems Specialis BS in related field Exp: 1-3 years in life science lab |
Implements Quality Systems programs that are consistent with company policies and regulatory standards. Audits and reviews quality data according to established procedures. Maintains tools for monitoring compliance training, corrective actions, audits, and document control. Supports corrective action task force initiatives | 11/2/2019 |
| 13423 | GeneDx Gaithersburg, MD NGS Lab Tech BS in medical technology Exp: 0-1 years |
A GeneDx NGS Lab Technician performs a higher than entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 11/2/2019 |
| 13424 | GeneDx Gaithersburg, MD DNA Extraction Technician BS in biology Exp: 0-1 years |
The Lab Technician performs all lab procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Prepares DNA dilutions and aliquots for use by downstream testing teams. Conducts diligent record-keeping and reporting. Prepares solutions. Performs equipment maintenance | 11/2/2019 |
| 13425 | GenerationBio Cambrige, MA Associate Scientist, (Molecular Biology, Analytical Development) BS in biological sciences Exp: 0-2 years |
Generation Bio seeks a highly motivated Research Associate to support analytical molecular biology activities in a cross-platform function. The successful candidate will work part of an analytics team responsible for the development and testing of research drug substance, as well as performing experiments to better characterize and understand the composition of our drug. Perform bioanalytical assays, including purity, copy number, expression, and activity assays to support the Production, Pre-clinical, and Process Development groups | 11/2/2019 |
| 13426 | Genewiz Cambridge, MA Laboratory Technician I, Genetic Analysis HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 11/2/2019 |
| 13427 | Genewiz South San Francisco, CA Laboratory Technician I HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 11/2/2019 |
| 13428 | Genewiz South Plainfield, NJ Laboratory Technician I, Molecular Biology Prep HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 11/2/2019 |
| 13429 | Genewiz South Plainfield, NJ Laboratory Technician I, Molecular Biology Prep HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 11/2/2019 |
| 13430 | Genewiz South Plainfield, NJ Sales Executive Continuous Recruitment- NY/NJ BS/BA in life sciences/biological sciences Exp: 1 year |
GENEWIZ is seeking technical sales professionals to join our New Jersey/New York based Sales team. Achieve annual sales goals within defined territory/accounts through the development, maintenance, and enhancement of customer accounts. Develop and implement an effective territory business growth plan. Retain current business baseline revenue by managing relationships with customers and other account contacts by collaborating with business leaders and the customer interface teams | 11/2/2019 |
| 13431 | Genewiz South Plainfield, NJ Bioinformatics Scientist MS in bioinformatics Exp: 1-3 years |
Work collaboratively with bench scientists, comprehend project objectives, evaluate and provide informatics solutions. Develop and implement bioinformatics analyses, applications, and workflows. Integrate statistical analysis to project design and data interpretations. Work closely with IT specialists to build robust infrastructure. | 11/2/2019 |
| 13432 | Genewiz South Plainfield, NJ Associate Scientist I, NGS BS/BA in biological sciences Exp: 1+ year in lab |
Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies . Communicate with customers by phone and e-mail in a friendly and professional manner | 11/2/2019 |
| 13433 | GenMark Carlsbad, CA Research Associate II MS in biochemistry, molecular biology, or chemistry Exp: 0+ years |
Conducts general molecular biology tasks, including nucleic acid purification, quantification, amplification and analysis on multiple platforms. Prepares reagents and solutions as needed, using appropriate procedural and documentation methods, including industry standard good laboratory practices. Identifies and solves problems in experiments or protocol designs, suggests improvements. Prepares documents meeting company standards, including data summaries, reports, SOPs and procedures | 11/2/2019 |
| 13434 | GenMark Carlsbad, CA Quality Control Specialist I BS in life science or engineering Exp: 0-3 years in QC |
This position conducts incoming, in-process and final release QC testing in a controlled manufacturing environment. This position may also execute validation studies, execute test protocols, analyze data, generate analytical reports, investigate Non-Conformance's, evaluate processes & procedures, utilize statistical techniques, review specifications, and inspect & test equipment. May conduct training on quality related tools, methods, and procedures. Interfaces with R&D, Manufacturing, Quality, and Supply Chain within the company and when appropriate with customers and suppliers on quality related issues. | 11/2/2019 |
| 13435 | GenMark Carlsbad, CA Research Associate II, Technology Development MS in biochemistry, molecular biology, or chemistry Exp: 0 years in bio lab |
The Research Associate II will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision for our technology development team. Conducts general molecular biology tasks, including nucleic acid purification, quantification, amplification and analysis on multiple platforms. Prepares reagents and solutions as needed, using appropriate procedural and documentation methods, including industry standard good laboratory practices | 11/2/2019 |
| 13436 | Genomatica San Diego, CA Research Associate I/II MS Exp: 0-2 years |
Genomatica is seeking a highly motivated Research Associate I/II, Microbiology/Molecular Biology to join the Strain Engineering team. This team is responsible for construction, characterization, evolution and characterization of host strains. The successful candidate will utilize her/his knowledge of Microbiology/Molecular Biology for cloning genes, genetically engineering chromosomal DNA, sequencing and analyzing the genome, characterizing product titers, growth and by-products when grown with various feedstocks. | 11/2/2019 |
| 13437 | Genomatica San Diego, CA Fermentation Associate I BS in Chemical/Biochemical Engineering, Bioengineering, Molecular Biology, Microbiology, or Biochemistry Exp: 1-4 years bio lab experience |
This position delivers high-quality fermentation data by applying optimal fermentor operating procedures, communicating observations clearly to Fermentation Science personnel, and works collaboratively to maximize experimental precision. This position will interface closely with the Fermentation engineers and scientists in the Fermentation Science Group to produce conclusive fermentation results that will guide process optimization and scale-up efforts | 11/2/2019 |
| 13438 | NeoGenomics Aliso Viejo, CA Project Data Administrator I AS/AA or higher Exp: 1 or more years in data entry |
The Project Data Administrator I works under general supervision to support Pharma Services projects with a focus on study data entry, QC, and associated documentation. You will support internal teams, data entry and QC activities for many projects at a time. This is the Early role in the Project Data Administrator job category. In this position, you will handle data and perform related tasks from a full range of projects including Molecular, IHC, Flow Cytometry, MultiOmyx, FISH, and Cytogenetics. | 11/2/2019 |
| 13439 | NeoGenomics Carlsbad, CA Clinical Laboratory Technologist I BS/BA in med technology, or chemical/biological/physical sciences Exp: 1+ year in clinical reference lab |
As a Clinical Laboratory Technologist I or II or III you will work under general supervision and you will be responsible for accurately performing highly complex laboratory testing procedures. You will determine acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. You will also analyze specimens, review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 11/2/2019 |
| 13440 | NeoGenomics Carlsbad, CA Client Advocate I HS Diploma/GED Exp: 1-3 years in customer service |
The Client Advocate I provides support and communications with NeoGenomics customers (physicians & medical staff) and couriers (FedEx and contracted couriers); as well as serves as the point of contact for internal customers such as territory business managers (sales), internal doctors, operational teams and senior leadership in relation to specialized diagnostic oncology testing via excellent telephone, written, and chat communication. This is the entry level in the Client Service organization and employees perform the full range of customer service activities; including inside sales functionality. | 11/2/2019 |
| 13441 | NeoGenomics Ft. Myers, FL Order Entry Specialist I - Data Integrity AS/AA Exp: 1+ year in healthcare/med billing |
As an Order Entry Specialist I, you will enter patient demographic characteristics and insurance information into a proprietary database using company specific software and internal documents. Additionally, you will input diagnosis codes, charges and verify insurance in accordance with company policies. | 11/2/2019 |
| 13442 | NeoGenomics Houston, TX Histotechnologist I AS/AA in histotechnology Exp: 1+ years related |
As a Histotechnologist I, II, III, you will work under general direction to precisely and accurately conduct a variety of routine and specialized histology procedures. You will research, troubleshoot, and resolve histology related inquiries and problems within the laboratory. This position requires you to produce the highest quality of embedding, microtomy, tissue grossing, tissue processing, and H&E staining, special staining and equipment maintenance. | 11/2/2019 |
| 13443 | NeoGenomics Aliso Viejo, CA Laboratory Assistant I HS Diploma Exp: 1-2 years |
As a Laboratory Assistant you will assist the department technologist in performing various basic laboratory procedures laboratory instrumentation to facilitate production. This in an entry level position in the clinical laboratory job category and employees in this position may not manipulate samples. | 11/2/2019 |
| 13444 | NeoGenomics Aliso Viejo, CA Accessioning Technician I AS/BS preferred, HS Diploma min Exp: 1+ year as acessioning technician |
As an Accessioning Technician I you will ensure proper handling of all specimens received and prepare specimens for laboratory testing. You will be performing functions such as matching patient information, data entry, and scanning documents. You will be responsible for reviewing all requisitions for missing information, working closely with Customer Care in order to obtain missing information in a timely fashion, and distributing new information to all departments involved. You will need to report problem holds and provide resolution in a timely fashion. | 11/2/2019 |
| 13445 | GenScript Piscataway, NJ Lab Technician - Ligation BS/BA Exp: 0-3 years |
We are looking for a Laboratory technician to assist our daily production tasks. The successful candidate should have biology or related science background, excellent time management skills, strong problem solving ability. He or she will need to work directly with production team, fit with collaborative and competitive culture in GenScript. | 11/2/2019 |
| 13446 | GenScript Piscataway, NJ Lab Technician - Plasmid Prep BS/BA Exp: 0-3 years |
We are looking for a Laboratory technician to assist our daily production tasks. The successful candidate should have biology or related science background, excellent time management skills, strong problem solving ability. He or she will need to work directly with production team, fit with collaborative and competitive culture in GenScript. | 11/2/2019 |
| 13447 | GigaGen South San Francisco, CA Research Assistant BS/BA Exp: 1-3 years lab experience |
GigaGen seeks a talented, highly motivated Research Assistant to work alongside PhD-level scientists on research funded by a $50 million co-development deal with Grifols, plus Phase II SBIR grants from the NCI and NIAID. This project involves high-throughput discovery and development of therapeutic antibody drug candidates from human and mouse immune repertoires. The work involves significant cell culture work, including a bioreactor and flow cytometry. | 11/2/2019 |
| 13448 | Gilson Middleton, WI Verification and Validation Specialist I BS/BA in sciences Exp: 0-3 years |
The job holder is introduced to and performs a wide variety of laboratory tasks and procedures related to the verification and validation of hardware and software products. Operates and maintains laboratory equipment and computers to perform product verification. Performs lab maintenance tasks. Conducts accuracy and precision analysis on liquid handling instruments. Uses lab methods (HPLC, SPE, PCR, bio-assays, etc.) to verify product function and design | 11/2/2019 |
| 13449 | Ginkgo Bioworks Boston, MA Research Associate - Protein Engineering BS/MS in biological sciences/engineering Exp: 1+ years in lab setting |
We are looking for someone who is excited about the field of synthetic biology and loves a challenge. We want a person who is eager to learn and has a desire to utilize automation to work more efficiently. Our ideal candidate will elevate our team through creative solutions while working closely with other foundry groups. Responsibilities include: Enzyme purification and characterization, Data analysis, Automation of protocols | 11/2/2019 |
| 13450 | Glaukos San Clement, CA Engineer, I BS in mechanical engineering Exp: 1-3 years |
Performs a variety of manufacturing engineering activities on ocular related products including manufacturing scale up, development, and sustaining activities. Responsibilities include developing creative solutions to manufacturing problems, development and execution of process, equipment, and product validations, ensuring the proper engineering deliverables are accurately generated, generation of 3D CAD models and 2D CAD drawings for assembly tools and fixtures, test procedures, project management and leadership, and maintaining schedule. May lead manufacturing related project teams with other engineers, technicians, and manufacturing staff with a focus on meeting manufacturing requirements with technically strong, high quality, cost effective approaches. | 11/2/2019 |
| 13451 | Glaukos San Clement, CA Regional Clinical Research Associate I BS/BA in biological sciences, nursing or related Exp: 0-2 years as CRA |
Lead/manage assigned sites through regular contact with investigators and site staff to monitor progress, answer questions, and provide guidance during the course of the clinical study. Critically review and analyze site activities through frequent visits and contacts to monitor study sites and performance. Travel to investigative sites to conduct site qualification, initiation, interim monitoring, and close-out visits | 11/2/2019 |
| 13452 | GenapSys Redwood City, CA Research Associate, NGS BS in biology, chemistry, biological engineering Exp: 1-2 years in lab |
The successful candidate will have a major impact on the direction of our core technologies, application direction and defining the next generation of GenapSys products. Formulation and test of amplification and sequencing reagents, on or ahead of schedule, utilizing qualified lab equipment, written, and/or verbal instructions. Ensure materials are ordered and in stock to meet formulation and testing requirements. Incoming QC of materials, including visual inspection and collecting data from automated leak testing. | 11/2/2019 |
| 13453 | Frontage Exton, PA Scientist-005 MS in chemical sciences Exp: 1 year in research chemistry |
For a CRO (Frontage Laboratories, Inc. – Exton, PA): design/develop method transfer, method development, validations, quantitation and structure elucidation; perform high-volume bio-analytical sample analysis; perform data analysis, data quality control (QC) and data interpretation for bio-analytical, PK, PD and ADME studies in regulated environment; utilize and maintain analytical instruments including Liquid Chromatography Tenderm Mass Spectrometry (LC-MS/MS), ultra-high performance liquid chromatography (UHPLC) with ultraviolet (UV) detector, Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Nuclear Magnetic Resonance (NMR). | 11/2/2019 |
| 13454 | Genentech Oceanside, CA Manufacturing Technician, BioProcess (Swing) BS/BA in engineering or life sciences Exp: 0-3 years |
Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, formulation, freeze thaw and transfer. Performs media/buffer solution preparation operations. | 11/2/2019 |
| 13455 | Genentech South San Francisco, CA BioProcess Technician BS in life science or engineering Exp: 1 year related |
The Bioprocess Technician will be be responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, formulation, freeze thaw and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). | 11/2/2019 |
| 13456 | Pace Analytical Maplewood, MN Lab Analyst - Optics BS in engineering, physics or related Exp: 0-1 years |
This candidate will perform routine lab experiments involving optics in a corporate research lab. The research project testing is completed as part of a process group in high throughput laboratory. RESPONSIBILITIES: Operate and maintain a variety of laser and optical testing instruments. Work with optical alignment on optical bench using light sources (white light, lasers, LEDs) and imaging systems (cameras, photodiodes). Sample collection, preparation, routine analysis, and interpretation results. etc. | 10/29/2019 |
| 13457 | Pace Analytical Maplewood, MN Chemist - HPLC & GC Pharmaceutical BS in chemistry or related Exp: 0-3 years |
Candidate will perform analytical testing to support product development of pharmaceutical inhalation devices. RESPONSIBILITIES: Assist higher level analysts with product or method development work. Follow established methods to complete stability testing. Provide testing of customer products using HPLC, UPLC, and some GC. Comply with FDA guidelines and SOPs in a cGMP environment. etc. | 10/29/2019 |
| 13458 | Pace Analytical Maplewood, MN Analytical Chemist BS in chemistry or related Exp: 1-2 years |
Seeking an analytical chemist to perform QC analysis of inhalation device components. RESPONSIBILITIES: Sample preparation and analysis using GC-MS and GC-FID. Testing methods using LC is also possible. Perform analysis on inhalation device components - performing extractable and QC testing on plastic, metal, and rubber components. Perform appropriate documentation of work in a GMP environment utilizing Electronic Lab Notebook (ELN), LIMS, and other software. etc. | 10/29/2019 |
| 13459 | PacBio Menlo Park, CA Senior Technician, Manufacturing BS in mechanical, electrical, optical, or industrial engineering Exp: No expeience necessary for BS candidates |
Pacific Biosciences is seeking a talented Senior Manufacturing Technician to align, test, and calibrate complex opto-mechanical DNA sequencing systems. Responsibilities: The Manufacturing Technician is responsible for building and testing complex third generation DNA sequencing instruments. Manufacturing technicians are responsible for on-time completion of assigned instrument builds while following a tightly defined process for recording test results, documenting encountered issues, and troubleshooting issues to resolution. Some additional responsibility may include highlighting process improvements, redlining documents, and providing feedback to manufacturing engineers. etc. | 10/29/2019 |
| 13460 | PACT Pharma South San Francisco, CA Senior Quality Control Associate MS Exp: 1+ year(s) |
We are currently recruiting for QC Associate, reporting to Manager of Quality Control. This position will be based in South San Francisco. | 10/29/2019 |
| 13461 | PACT Pharma South San Francisco, CA Research Associate MS in immunology, immuno-oncology, or related Exp: 1+ year(s) |
We are currently recruiting for Research Associate in the Tumor Immunology group. The person in this role will be responsible for performing immunological assays to functionally characterize the patient private NeoE-specific T cells, as part of product selection for the manufacture of the adoptive cell therapy product (neoTCR-P1). This process is performed in a GMP-like laboratory setting. The candidate should enjoy operating in an exceptionally dynamic and cooperative environment and will communicate results to and coordinate efforts with a larger cross-disciplinary team of immunologists, biologists, engineers and bio-informaticians. | 10/29/2019 |
| 13462 | PAR Pharmaceutical Rochester, MI Chemist II MS in chemistry, chemical engineering, or related Exp: 1+ year(s) |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. etc. | 10/29/2019 |
| 13463 | PAR Pharmaceutical Rochester, MI Process Engineer I MS in engineering or chemical engineering Exp: 1+ year(s) |
The Process Engineer I, with guidance, performs various duties related to optimization and analysis of production processes, new products, processes and technology transfers. Prepare and execute engineering study protocols, manufacturing and packaging experimental / feasibility study / validation batch records and protocols and complete interim and / or final summary reports for marketed and new products. Perform or assist on-site and site-change technical transfer, scale-up or scale-down factor evaluation, manufacturing / packaging process and equipment troubleshooting, and SOP preparation and review. etc. | 10/29/2019 |
| 13464 | Paragon Gene Therapy Harmans, MD Quality Assurance Associate I/II - Floor Support BS in an engineering or science field Exp: 1 year |
Quality Associate I or II (QA Floor Support) is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product to be used for human consumption. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. etc. | 10/29/2019 |
| 13465 | Paragon Gene Therapy Harmans, MD Manufacturing Associate I - GMP Bioprocess AS/BS in a scientific or engineering discipline Exp: 0-1 years |
The Manufacturing Associate performs and documents cGMP activities to support upstream or downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed. Key Responsibilities: Performs Processing Steps and/or Manufacturing Support activities, monitoring process against the batch record. etc. | 10/29/2019 |
| 13466 | Paramit Morgan Hill, CA Manufacturing Engineer 1 BS in mechanical, electrical, or industrial engineering Exp: 0-1 years |
Entry manufacturing engineering role in a dynamic and fast growing manufacturing company. Working with advanced products and processes in the revolutionary life sciences and medical instrumentation industry. Providing technical support to our manufacturing operations to overcome challenges and implement solutions. | 10/29/2019 |
| 13467 | Paramit Morgan Hill, CA Test Development Engineer I BS in mechanical, electrical, or industrial engineering Exp: 1 year |
The Manufacturing Test Development Engineer I learn the inside details on the test development that includes creating test programs for AOI ( automated optical inspection ), AXI ( automated x-ray inspection ) and ICT ( in-circuit test ). The engineers get to use their analytical skills to create a suite of test scripts that can detect defects that human eye cannot catch and produce high quality PCBA products. | 10/29/2019 |
| 13468 | PBL Assay Science Piscataway, NJ Assay Services Scientist I/II BS in a life science Exp: 1+ year(s) |
The Assay Services Scientist I / II works primarily with cell culture-based bioassays, executing antiviral bioassays, ELISAs and other highly sensitive immunoassays for characterizing proteins and reagents; analyzing data and drafting client reports; and developing new and custom assays to support the growth of the Assay Services Group. ESSENTIAL DUTIES AND RESPONSIBILITIES: Execute immunoassays on ELISA, and other highly sensitive platforms like Electrochemiluminescence (MSD), Single Molecule Array (Simoa), and Single Molecule Counting (Erenna). Execute antiviral and antiproliferative cell-based bioassays. etc. | 10/29/2019 |
| 13469 | PBL Assay Science Piscataway, NJ Laboratory Technician BS in a biological science Exp: 0-3 years |
The Laboratory Technician is responsible for product manufacturing and ELISA kit optimization and stability testing following established guidelines and procedures and completing required documentation. The individual will routinely analyze raw data and generate summaries of work performed in compliance with Standard Operating Procedures (SOPs). The Laboratory Technician will make judgements based on knowledge and expertise as to the accuracy and reliability of analytical results; identify and report problems with results to supervisor; participate in investigations and data analyses; and troubleshoot instruments and methods. etc. | 10/29/2019 |
| 13470 | PBL Assay Science Piscataway, NJ Quality Control Scientist I BS in a biological science Exp: 1-2 years |
To ensure the quality of PBL reagents the Quality Control (QC) Scientist I will perform release and stability testing of interferons, antibodies, and manufactured ELISA kits. In addition, the QC Scientist I will perform bioassays or immunoassays to troubleshoot relevant customer issues and design and initiate experiments and projects to improve the quality of PBL products. The QC Scientist I may also serve as back up to the Product Development, Assay Services, or Manufacturing departments as needed: such additional duties may include designing and performing ELISA testing protocols, custom bioassays, and solution preparation. etc. | 10/29/2019 |
| 13471 | PBL Assay Science Piscataway, NJ R&D Scientist I MS Exp: 0-2+ years |
The R&D Scientist is responsible for the hands-on development of immunoassays, such as ELISAs and cell-based assays, for commercial production. This individual plans and executes design, development, and Manufacturing transfer of bioanalytical assays for product commercialization. The R&D Scientist is also responsible for development of custom assays and reagents for clients. etc. | 10/29/2019 |
| 13472 | Penumbra Roseville, CA Quality Engineer BS in an engineering or science field Exp: 1-5 years |
As a Quality Engineer at Penumbra, you will participate in all aspects of product manufacturing in order to ensure the highest level of quality in new and existing products, and their compliance to applicable regulations and standards. You will apply your passion for detailed analysis to identifying problems and determining the appropriate course of action. You will be looked to for ensuring compliance and building a culture of quality within your project teams. etc. | 10/29/2019 |
| 13473 | Performance Validation unspecified, Level 1 Staff Validation Specialist BS in the life sciences or related Exp: Entry level |
Performance Validation is seeking full-time Level 1 Validation Engineer/Specialists in the following locations: Indiana, Michigan, Illinois, and Kansas. The Level 1 Validation Engineer/Specialist is an entry level position and reports directly to the Division Director or Manager and is assigned to one or more project teams to perform work for Performance Validation’s customers. etc. | 10/29/2019 |
| 13474 | Performance Validation unspecified, Level 1 Staff Validation Engineer BS in mechanical, chemical, or biomedical engineering Exp: Entry level |
Performance Validation is seeking full-time Level 1 Validation Engineer/Specialists in the following locations: Indiana, Michigan, Illinois, and Kansas. The Level 1 Validation Engineer/Specialist is an entry level position and reports directly to the Division Director or Manager and is assigned to one or more project teams to perform work for Performance Validation’s customers. etc. | 10/29/2019 |
| 13475 | Personalis Menlo Park, CA Laboratory Assistant (Temp to Perm) BS in molecular biology or related Exp: 0-2 years |
We are looking for a team-oriented Laboratory Assistant to join our operations team. The ideal individual must have the ability to think on their feet and troubleshoot issues. Within a dynamic startup environment, the successful candidate, under direction of the Laboratory management, will help grow the sequencing services laboratory. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. This position is 3 months temp to Perm. etc. | 10/29/2019 |
| 13476 | Personalis Menlo Park, CA Research Associate - Operations (Temp to Perm) BA/BS in a biological discipline Exp: 0-2+ years |
Located in Menlo Park, CA, we are seeking a talented and highly motivated Research Associate to join our Operations Team. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. This is a 3 months temp to hire position. We have Multiple openings for swing and day shifts that include one weekend day (Tues - Sat or Sun - Thurs). etc. | 10/29/2019 |
| 13477 | Pace Analytical Naperville, IL Lab Analyst - Chemical and Physical Testing AS/BS in chemistry, biology or a related science Exp: 0-2 years |
The main function of a laboratory technician is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. RESPONSIBILITIES: Monitor product quality to ensure compliance to standards and specifications. Set up and conduct chemical experiments, tests, and analyses using techniques such as chromatography, spectroscopy, physical and chemical separation techniques, and microscopy. etc. | 10/29/2019 |
| 13478 | Pace Analytical Maplewood, MN Molecular Biologist BS in chemistry, biology or related Exp: 0-1 years |
Seeking a Lab Analyst to perform laboratory methods relating to molecular biology. This candidate will perform chemical detection testing as part of a quality and manufacturing team relating to food safety products. This candidate will perform routine testing and report writing per lab protocols. Work is performed in a fast-paced lab setting. etc. | 10/29/2019 |
| 13479 | Pace Analytical Maplewood, MN Regulatory Data Specialist BS in chemistry, biochemistry or related Exp: Entry level |
This candidate will work with vendors to seek out chemical information in an entry-level regulatory services position. This is a great entry-level position to learn global chemical regulations for a wide range of materials. This is a non-laboratory position. etc. | 10/29/2019 |
| 13480 | Pace Analytical Eagen, MN Lab Analyst - Chemical Testing BS in chemistry or related Exp: 0-2 years |
The Lab Analyst will conduct qualitative and quantitative chemical analyses in laboratories for quality, process control or to develop new products or knowledge. They are responsible for creating new products and processes or improving existing ones for clients. They will work in a small team (2-4 people) that is a part of a much larger team (40+). Once trained, the role requires a hardworking candidate that can multitask, easily adjust to different tasks based on daily demand, and prioritize project work. etc. | 10/29/2019 |
| 13481 | Facet Atlanta, GA QUALITY ENGINEER BS in engineering or sciences Exp: 1-3 years in quality engineering |
The Quality Engineer plans and directs activities concerned with development, application, and maintenance of quality processes, materials, and products. Additionally, responsible for investigation manufacturing and customer nonconformance’s, determining root causes and corrective actions, reviewing and approving protocols and final reports and developing product specifications and sampling plans. | 10/27/2019 |
| 13482 | Fate Therapuetics San Diego, CA Research Associate, Cancer Immunotherapy BS in biological sciences Exp: 0-3 years in lab setting |
The candidate’s primary responsibility will be to generate lentivirus for editing and production of CAR-T cells in support of research efforts at Fate. Experience with current molecular biology techniques used for editing and engineering of hematopoietic cells is highly desired. The successful candidate will have excellent oral and written communication skills. | 10/27/2019 |
| 13483 | Fate Therapuetics San Diego, CA Clinical Trial Associate BS/RN in relevant sciences Exp: 1 or more year hands on experience in clinical trial management |
Fate’s clinical operations group is seeking amotivated and talented individual to support development and management of an electronic trial master filesystem(Veeva)and assistour clinical trial managerswith administrative and project-specific support related to the conduct of clinical studies. The successful candidate will assure adherence to protocol(s) and GCP/ICH guidelines and applicable regulations. The ideal candidate will be familiar withphase I-IV protocols and have hands-on experience in developing and maintaining electronic clinical trial management systems. | 10/27/2019 |
| 13484 | Ferring Parsippany, PA Technician, QC Micro (2nd Shift) BS/BA or MS in biology or related Exp: 1 year in QC microbiology |
To perform laboratory QC Microbiological testing for in-process and finished product, water sampling testing, and routine and batch processing environmental monitoring in aseptic classified cleanrooms. Perform Bioburden, Endotoxin, Total Plate Count, Coliform, Bacteriostasis &Fungistasis (B&F) and Biological Indicator testing. Perform clean utilities (compressed air, Nitrogen, WFI/DIW and Clean Steam) sampling and testing. Initiate and investigate microbiology related deviations (NCEs/NOE), OOS investigations, and implementing appropriate CAPAs as needed. | 10/27/2019 |
| 13485 | Ferring Parsippany, PA Process Equipment Engineer BS/BA in sciences or engineering Exp: 0-2 years |
Responsible for process equipment engineering, overseeing, guidance, scheduling and coordination required to fully implement process equipment engineering projects in order to support manufacturing, QA, Tech services, IT, Procurement, other departments, external vendors and government agencies as required. The incumbent is considered a Subject Matter Expert (SME) responsible for all aspects of production equipment (complete sterile manufacturing train) and its interfaces including mechanical, electrical, process plumbing, and safety interfaces. The incumbent must have superior troubleshooting and problem solving ability to ensure minimal down time and interruption to production schedule. The incumbent interacts with Production, QA, Tech services, IT, and other departments as necessary obtain all applicable stake holder(s) information and decisions to collaborate high quality low risk results. | 10/27/2019 |
| 13486 | Bfibrocell Exton, PA GMP Support Technician AS/AA Exp: 1 year |
The GMP Support Technicianwill perform a variety of tasks in support of the daily production of sterile cell therapy product. Operations are predominately performed within a cleanroom environment under Current Good Manufacturing Practices (CGMP) conditions. Provides operational support for manufacturing activities including media/reagent preparation, kitting, cell freezing and equipment/materials staging. Follow batch records, SOP’s and other cGMP documentation; complete all documentation in a clear and concise fashion | 10/27/2019 |
| 13487 | Finch Somerville, MA Research Associate BS/BA in biological sciences Exp: 1-2 years industry experience |
Finch is looking to hire a detailed-oriented and driven Research Associate, Analytical Development, who will be responsible for developing and conducting analytical methods for drug products in Finch’s pipeline. This individual will ensure Finch microbial products meet standards by performing microbial analytical procedures to characterize in-process and commercial microbial samples. As an integral part of this team, the successful candidate will carry out laboratory work, establish protocols, and support cross-functional teams in Research and Development, Quality and Manufacturing. This position reports to the Senior Scientist. | 10/27/2019 |
| 13488 | Finch Somerville, MA Process Development Engineer BS/BA in chemical/biomedical engineering, or related Exp: 1-3 years |
Assist with troubleshooting, root cause analysis and identification of corrective actions to support Pharmaceutical Development or GMP Manufacturing equipment and process issues. Support efforts to scale-up & undergo technical transfer of production processes to GMP Manufacturing. Lead planning, execution, and documentation of studies related to design of novel drug products. Work cross-functionally across Quality, Research, Clinical, and Manufacturing teams to achieve company goals. | 10/27/2019 |
| 13489 | Flexion Multiple Locations, NA Flex Sales Representative BS/BA Exp: 1-3 years sales experience |
Promote Flexion's product(s) via the telephone (outbound and/or inbound calls) and in person (field visits) by engaging assigned HCP targets in in-depth program discussions to attain individual, territory and company goals for sales, market share, etc. In preparation for field activities when deployed to assigned territory or as part of vacancy management coverage. Coordinate and align a strategic field call plan with the Regional Sales Director prior to deployed into vacant territory. Verify and complete required data entry into the CRM systems, such as details of the target’s responses and any follow-through actions. | 10/27/2019 |
| 13490 | Fluke Omaha, NE Sales Engineer BS/BA in engineering or technical field Exp: 0-3 years |
You will be working under the leadership of a Sr. Sales Engineer using your technical knowledge to support key sales efforts with our manufacturer representative agencies, distribution partners, and end-users and proactively set and meet stretch goals. Actively promote products and solutions and achieve sales quota by building rapport, providing training and support, and making end user calls with representative agencies and distribution account managers. Work under the direction of the Sr. Sales Engineer to drive the activities and performance of assigned representative agencies. | 10/27/2019 |
| 13491 | Fluke Everette, WA Quality Engineer BS in engineering Exp: 1-3 years in quality improvement |
The Quality Engineer II will provide quality engineering and continuous improvement leadership to the operations, engineering, and quality organizations within Fluke at our headquarters in Everett, WA. They will be responsible for employing advanced quality engineering tools and the Fortive Business System tools in partnership with design and sustaining engineering, procurement, supplier quality, and operations to achieve continuous improvement in product safety, reliability and cost of quality. | 10/27/2019 |
| 13492 | FORMA Therapeutics Watertown, MA Research Assoc/Sr Research Assoc, Biology BS or MS in biology Exp: 0-2 years |
The Biology Team at FORMA Therapeutics seeks a Research Associate/Senior Research Associate with a strong background in cancer biology to contribute to FORMA’s pre-clinical and clinical projects. The ideal candidate will be a highly motivated individual with a strong technical background in cancer biology. Develop, optimize and perform assays using molecular biology procedures and technologies including qPCR, quantitative western blots, ELISA. In vitro culture of cancer cell lines and primary cells as well as blood/tissue is required. | 10/27/2019 |
| 13493 | Foundation Medicine Cambridge , MA Billing and Reimbursement Associate HS Diploma/GED Exp: 1+ years in customer service |
The Associate, Billing and Reimbursement contributes to the overall patient access to FMI products through support and education. The position supports the daily queues of incoming accessioned cases to review for complete and accurate billing information to determine the party responsible for payment, including benefits investigation and prior authorization processing. The incumbent acts to minimize reimbursement as a barrier to receiving physician orders and is responsible for answering questions by internal and external customers on billing inquiries, working with third party insurance companies and completing manual charge entries. | 10/27/2019 |
| 13494 | Foundation Medicine Cambridge , MA Molecular Technologist I BS in biology or life sciences Exp: 1 year in CLIA/CAP lab |
We are currently looking to add to our Clinical Lab staff at various levels and shifts. Perform highly complex testing according to established SOPs (NGS library prep, hybridization, and sequencing). Operate automated 8-span and 96-head liquid handling platforms for sample processing. Complete projects fitting of level of expertise and is able to deliver results with minimum guidance. | 10/27/2019 |
| 13495 | Foundation Medicine Cambridge , MA Laboratory Research Assistant BS in biological sciences Exp: 1+ year in science/technical work |
The Laboratory Research Assistant I is a core member of the Product Development team. This position supports all Product Development laboratory personnel who are developing the next generation of diagnostic assays. This position may include equipment maintenance, sample repository management, and reagent preparation in addition to other tasks in a highly complex laboratory environment. | 10/27/2019 |
| 13496 | Foundation Medicine Cambridge , MA Client Services Representative I - Temp to Perm HS Diploma/GED Exp: 1 or more in service field |
The Client Services Representative is a vital position at FMI tasked with the responsibility of responding to and resolving a wide range of client inquiries and requests as well as acting as a liaison between departments within FMI, and between FMI and its partners, customers and the patient. The incumbent operates in a supportive function within the fast-paced Client Services department. | 10/27/2019 |
| 13497 | Foundation Medicine Cambridge , MA Client Services Representative I - Mid Shift (Temp to Perm) HS Diploma/GED Exp: 1 or more in service field |
The Client Services Representative is a vital position at FMI tasked with the responsibility of responding to and resolving a wide range of client inquiries and requests as well as acting as a liaison between departments within FMI, and between FMI and its partners, customers and the patient. The incumbent operates in a supportive function within the fast-paced Client Services department. | 10/27/2019 |
| 13498 | Fresenius Kabi Canton, MA CHEMIST, METHOD DEVELOPMENT MS in chemistry Exp: 1-3 years |
The Chemist, Method Development has broad expertise in routine as well as complex chemical methods of analysis. The incumbent conducts all aspects of Quality Control testing including method development, method validation, experimentation, routine and non-routine quality control testing, and record keeping. The incumbent must be able to develop, validate, and implement methods that meet project needs. The incumbent is typically assigned the more complex test methods due to their advanced training in specialized methods of analysis. The position is responsible for conducting studies with increasing complexity in nature and solving problems to ensure a robust method can be performed in the laboratory. | 10/27/2019 |
| 13499 | Fresenius Kabi Grand Island , NY QC TECHNICIAN II Microbiology 2nd Shift AS/AA or BS/BA in life sciences, animal technologies, etc. Exp: AS/AA: 1-2 years, BS/BA: 0 years |
This position serves in the capacity of performing general laboratory tasks of testing finished products, stability, raw material, utilities, and monitoring for environmental control, as well as supporting validations of rooms, equipment and materials. This position reports to the supervisor for the functional area to which they are assigned and has no direct reports. The QC Technician II position works closely with other departments, such as validations, chemistry, Operations, Product Development, Quality Systems and Product Release to assure the support of the Microbiology department on various projects, studies and routine tasks. | 10/27/2019 |
| 13500 | Fresenius Kabi Chicago, IL VALIDATION ENGINEER BS/BA in science or engineering Exp: 1-3 years in cGMP facility |
Responsible for providing technical support to operations in terms of equipment/system/process initial validation and equipment/system/process requalifications. Will participate in process and equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. The individual must become certified to enter Controlled Areas of the plant (class 100, 10,000 and 100,000). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 10/27/2019 |
| 13501 | Fresenius Kabi Grand Island , NY ASSOCIATE INVESTIGATIVE WRITER BS/BA Exp: 1-2 years in pharma manufacturing or cGMP |
Works with Supervision and Investigative Writers to efficiently and thoroughly investigate deviations and customer complaints, determination of root cause, and initiation of corrective/preventative actions designed to adequately address and correct the quality related deficiencies identified during the investigation process. Responsible to recommend proactive corrections, corrective actions and preventative actions based on noted trends to minimize the potential for repeat incidents that may lead to, or result in, the issuance of product discards, field actions, or recalls. The position requires working with moderate supervision to manage assigned investigations from initiation to completion. | 10/27/2019 |
| 13502 | Fresenius Kabi Grand Island , NY ASEPTIC CONTROL OPERATOR I HS Diploma/GED Exp: 0-2 years |
Responsible for the operation and performance of high speed pharmaceutical equipment in a clean room (class 100) environment. Aseptic Control Operators are responsible for the cleaning, changeover, setup, startup, operation, and breakdown of filling lines. Additionally, they may be assigned tasks related to the general upkeep of the clean rooms, such as unloading ovens and sterilizers, performing routine cleaning, and performing minor maintenance. All of these activities are governed by strict procedures and regulations and require a high degree of training. Therefore, Aseptic Control Operators must complete all required training, and follow all applicable Standard Operating Procedures, Batch Records, and Protocols, and must be familiar with current Good Manufacturing Practices. | 10/27/2019 |
| 13503 | Fresenius Kabi Bensenville, IL ASSOCIATE SUPPLY CHAIN ENGINEER BS in industrial engineering Exp: 1-3 years |
Assists in observation, data collection, and data analysis used in the improvement of all distribution center operational processes, including inbound, outbound, and inventory control functions for the US Fresenius Kabi finished goods distribution network. This role will report to the Senior Manager Supply Chain Solutions. | 10/27/2019 |
| 13504 | Fluke Glenwood, IL Laboratory Technician II BS/BA in life sciences Exp: 1-2 years related experience |
The following list includes a sample of the tasks a person in this role would need to perform. Calibrates radiation detection equipment using ionizing radiation sources/techniques. Assures customer satisfaction and on time delivery of calibrated devices . Collects documentation, performs evaluations, and corrects anomalies in calibration laboratory activities and under guidance implements preventative measures to eliminate reoccurrence of incidents. | 10/27/2019 |
| 13505 | Fate Therapuetics San Diego, CA Quality Control Associate BS or MS in biological sciences Exp: BS: 1+ years lab experience, MS: 0 years |
The successful candidate will execute and analyze experiments to assess thecharacteristicsof hematopoietic and stem cell-based therapeuticsundercGMP environment. Candidates musthave experience working withmammalian cell culture, and analysis of data from cell-based assays, especiallyddPCR or flow cytometry. Performmulti-parameterflow cytometry, ddPCRand other cell-based assays to support Fate’s clinical programs including testing of samplesfrom ongoing clinical trials and from manufacturing processes | 10/27/2019 |
| 13506 | Fate Therapuetics San Diego, CA Quality Assurance Associate BS/BA in scientific discipline Exp: 1 year in material disposition |
The successful candidate will assure adherence to standard operating procedures,GXPguidelines,and applicable regulations. The ideal candidate will have experience working in a cGMP environment, and have hands-on experience in material enrollment, receipt, and disposition. Proactively maintain an understanding of regulations and best practices for a robust Quality Management Systeme.g. FDA, USP, ICH, etc. Performing routine inspection/assessment/disposition on all incoming materials. | 10/27/2019 |
| 13507 | Ferndale Pharma Group Ferndale, MI Customer Service Specialist HS Diploma/GED Exp: 1-3 years in customer service |
Ensures the basic mission of Biopelle, Inc. of being “the most trusted partner of the Aesthetic Medicine Community” is maintained while servicing all physicians and customers in a professional and ethical manner. Helps implement positive, proactive and results oriented strategies and tactics to ensure superior customer service that exceeds customer expectations. Implements policies and procedures to ensure timely and accurate performance of order taking, order processing, data base upkeep, customer requests, and customer contacts. | 10/27/2019 |
| 13508 | Endo Pharmaceuticals Chicago, IL Sales Representative - Chicago BS/BA Exp: 1 year in business/biopharma/sales |
Accomplishes targeted sales and increases the market share of key (bio) pharmaceutical products. Calls on a select number of high value physicians in a specified geographic area and focuses on establishing durable relationships, effectively delivering product information, and aiding in training. Helps customers develop reliable processes for reimbursement and access. Is comfortable providing information to the entire office staff and has the ability to identify new sales opportunities and leads in their territory. | 10/26/2019 |
| 13509 | Endo Pharmaceuticals Harsham, PA Manufacturing Associate l DSP BS/BA Exp: 0-3 years in biopharmacuetical manufacturing |
The Manufacturing Associate I – Fermentation works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture Collagenase Clostridium Histolyticum (CCH) bulk drug substance (BDS). This role is responsible for supporting necessary fermentation and production activities, including validation and development work as needed. | 10/26/2019 |
| 13510 | Envigo Cumberland, VA Study Technician II AS/AA or BS/BA in life sciences, animal technologies, etc. Exp: 6 months as animal technican |
To collect, document, and manage pertinent data including animal observations, test material administration, and clinical sample collection in compliance with appropriate SOPs and regulatory agency guidelines. To monitor animal health and welfare in compliance with the Animal Welfare Act and help maintain facilities for AAALAC compliance. Assess and document clinical observations, body weight data, food consumption data, environmental data, and other data on the appropriate data collection system (or by hand when necessary). | 10/26/2019 |
| 13511 | Envigo Alice, TX Vet Tech 1 AS/AA or BS/BA in life sciences, animal technologies, etc. Exp: 6 months as animal technican |
Works closely with the veterinary staff in supporting the nonhuman primate (NHP) colonies in Alice, TX. Monitors animal health and welfare with the opportunity to work with different NHP species. Position includes assisting all departments onsite including the hospital, behavior, quarantine, shipping and outside colony teams. Performs technical medical procedures in the various departments and assists the veterinary team in all aspects of animal care. | 10/26/2019 |
| 13512 | Envigo Madison, WI Machine Operator HS Diploma/GED Exp: 0-2 years |
Machine Operator to operate equipment to produce high quality diet in accordance with Envigo Teklad standards. Operate automated manufacturing process in accordance with established standard operating procedures. Follow production instructions of immediate supervisor to insure a safe work environment. To ensure a safe work environment; wear all PPE and all established safety procedures without exception. | 10/26/2019 |
| 13513 | Envigo Cumberland, VA Animal Care Technician HS Diploma/GED Exp: 0-2 years |
Conduct routine husbandry and animal health procedures in accordance with departmental SOP’s and maintaining USDA and AAALAC compliance. Operate the power washer to clean and sanitize runs, feeders, walls, building and floors per SOPs. Ensure that all occupied runs have adequate feed available at all times. Perform general house cleaning throughout the support areas. Humane care and treatment of animals. | 10/26/2019 |
| 13514 | Envigo Indianapolis, IN Animal Care Technician HS Diploma/GED Exp: 0-2 years |
To care for laboratory animals, their environment, and maintain records of their productivity and growth. To learn how and to maintain animals in inventory, to prepare animals for shipment, and to medicate or inject animals. Provide food, water, and clean housing to animals according to a rigid schedule. Maintain detailed records of animal production and inventory in precisely weighed and aged groups. | 10/26/2019 |
| 13515 | Enzo Biochem Farmingdale, NY Medical Technologist- Generalist BS/BA in lab science, medical technology, etc. Exp: 1 year in medical lab |
The Medical Technologist will perform qualitative and quantitative tests and examinations using various analyzers and/or manual methods on specimen sources such as blood, urine, and other body fluids using established procedures. They will also be responsible for performing established quality assurance procedures (quality control testing, instrument function checks and calibrations). Maintains appropriate documentation and reports irregularities. | 10/26/2019 |
| 13516 | Abcam Cambridge, MA Logistics Technician HS Diploma/GED or BS/BA Exp: Entry Level |
Process incoming shipments from suppliers, ensuring accuracy of all product data. Aliquot product into vials and assemble kits for customer orders and global stocking. Work with colleagues across the business to resolve discrepancies quickly. Maintain accurate inventory levels using both manual and automated systems. Fulfill customer orders using internal systems and processes, ensuring accuracy of all products in all orders. Work with teammates to improve the efficiency and accuracy of any processes implemented within the Logistics Department using creativity and resourcefulness. | 10/26/2019 |
| 13517 | Abcam Burlingame, CA Research Associate - IVD BS in biological sciences Exp: 1-2 years in biological sciences |
Based in our Burlingame Office, this manufacturing position is a great opportunity to transition into the medical device Industry! This role will be responsible for carrying out GMP manufacturing of IVD IHC primary antibodies according to the requirements of SOP’s, batch production records, and approved protocols. Perform immunohistochemical (IHC) stain for development or manufacturing of IHC antibody, staining kits and ancillary reagents. | 10/26/2019 |
| 13518 | Eurofins West Point, PA Biochemist BS/BA in biochemistry, biology, chemistry Exp: 1-3 years |
Perform assays on vaccine products, process intermediates, and related experimental samples using SDS-Page, Capillary Electrophoresis, ELISA, Biacor, nucleic acid quantification and other biochemical/analytical tests(e.g., spectrophotometric, electrophoretic, immunochemical methods). Maintain records and test results following good manufacturing practices (GMP). | 10/26/2019 |
| 13519 | Eurofins Malvern, PA Bioassay Method Development Scientist BS or MS in sciences Exp: 0-2 years |
Perform method development, optimization, validation, and transfer of Bioassays. Immunoassays and PCR analysis. Troubleshoot method and instrumentation problems. Initiate and perform investigations. Carry out method transfers and feasibility studies. Validation protocols and reports | 10/26/2019 |
| 13520 | Eurofins Columbia, MO Associate Scientist, Stability and Batch Release MS in biological sciences or engineering Exp: 0-2 years |
he Associate Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. | 10/26/2019 |
| 13521 | Eurofins Columbia, MO Associate Scientist, Biotech MS in biological sciences or engineering Exp: 0-2 years |
Eurofins BPT-Columbia is looking for an Associate Scientist to join our Biotech team located in Columbia, Missouri. The Associate Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. | 10/26/2019 |
| 13522 | Eurofins Kalamazoo, MI Associate Scientist BS/BA in biolgical sciences, or chemistry Exp: 0-2 years |
Protein purification (mAbs, therapeutic proteins, reagent proteins) by affinity, ion-exchange, HIC, or other native methods. Use and troubleshoot the AKTA suite of purification instruments and automated high-throughput systems. Analytical characterization of proteins by SDS-PAGE, CGE, Western Blot, and analytical SEC. Quantitate proteins by UV and BCA assay. Maintain electronic laboratory notebooks and records in accord with scientific protocol | 10/26/2019 |
| 13523 | Eurofins Dayton, NJ Analytical Chemist BS/BA in biolgical sciences, or chemistry Exp: 0-2 years |
Assist the Study Director with all phases of study design, scheduling and conduct. Act proactively to identify problems and potential problems. Assist in writing, reviewing and editing reports, protocols and SOP’s. Set-up and conduct experiments in accordance with Protocol and SOP's. Efficiently carry out procedures necessary to complete each project with minimal supervision. Meticulously maintain precise records of all experiments in accordance with good laboratory practices. | 10/26/2019 |
| 13524 | Eurofins Phoenix, AZ 3rd Shift Aseptic Manufacturing Associate HS Diploma/GED Exp: 6 months in GMP manufacturing |
Manufacturing Associate performs a variety of environmental service duties to maintain and sterilize the manufacturing suite and equipment. Ensure all cleanroom areas and equipment are clean, disinfected and ready for production of sterile medical products. Operate Microsoft Applications (for charting, presentations, etc.) and other computer based systems utilized in the manufacturing department (i.e., MES, HMIs, etc.). Follow standard procedures and execute activities independently, as well as in a team environment | 10/26/2019 |
| 13525 | Evonik Milton, WI Operations Technician HS Diploma/GED Exp: 0-2 years production experience |
Fill pails, drums, and totes with raw materials, intermediates, and finished products (including forklift operation). Run reactors/product blends per operating directions. Clean transfer lines within the plant and to the drumming station. Unload empty packages and stage for use, load box trailers with product for transfer. Maintain good housekeeping, perform housekeeping audits, run karl fisher analysis on titrators, and assist in filter change-outs, perform fork-lift inspections, etc. | 10/26/2019 |
| 13526 | Evonik Janesville, WI Plant Process Engineer BS or MS in chemical engineering Exp: 1-2 years process engineering |
Support and execute plant productivity projects to drive continual improvements in the areas of growth, expansion, production capacity and cost reduction to meet business and OPTECH initiatives and targets. Generate detailed scope of work documents for CAPEX and plant expense based projects that include equipment and safety device sizing and specifications, piping design, materials of construction, control strategies and safety circuits and procedures. Provide day-to-day process engineering and technical support to plant operations including troubleshooting efforts. Support and execute plant productivity projects to drive continual improvements in the areas of growth, expansion, production capacity and cost reduction to meet business and OPTECH initiatives and targets. Generate detailed scope of work documents for CAPEX and plant expense based projects that include equipment and safety device sizing and specifications, piping design, materials of construction, control strategies and safety circuits and procedures. Provide day-to-day process engineering and technical support to plant operations including troubleshooting efforts. | 10/26/2019 |
| 13527 | Evonik Lafayette, IN Process Engineer BS in chemical engineering Exp: 0-2 years |
Apply process engineering knowledge and skills to support the synthesis of starting materials pharmaceutical intermediates and final bulk products in a safe, efficient and environmentally responsible manner. Specifically, the process engineer is responsible for demonstrating process understanding, monitoring, and managing process performance. | 10/26/2019 |
| 13528 | Exelixis Alameda, CA Outsourcing Operations Analyst I MS/MA Exp: 1 year related experience |
This role assists with financial operations and reporting in Global Strategic Outsourcing Department. Responsibilities include supporting the Associate Director with contract administration, budget estimates, payment processing and reporting to facilitate the outsourcing strategies and activities of the Research & Development Organization. This role also requires the ability to obtain appropriate information to administer contracts and payments for outsourced agreements and communicates regularly to internal and external stakeholders on status of contracts and payment requests. | 10/26/2019 |
| 13529 | Exelixis Alameda, CA Outsourcing Operations Analyst I MS/MA Exp: 1 year related experience |
This role assists with financial operations and reporting in Global Strategic Outsourcing Department. Responsibilities include supporting the Associate Director with contract administration, budget estimates, payment processing and reporting to facilitate the outsourcing strategies and activities of the Research & Development Organization. This role also requires the ability to obtain appropriate information to administer contracts and payments for outsourced agreements and communicates regularly to internal and external stakeholders on status of contracts and payment requests. | 10/26/2019 |
| 13530 | Biotechne San Jose, CA Manufacturing Technician I AA or HS Diploma/GED in biotech, chemistry, biology Exp: 1+ years in manufacturing |
Bio-Techne’s Protein Platform Division is looking for a Manufacturing Technician with a motivation to participate in the growth of a fast-paced company engaged in cutting edge biological research. The successful candidate will work with other members of the Reagent production team to make great products, performing tasks involving plate filling, labeling, vialing, and finishing materials. Operation of semi-automated liquid dispensing equipment is integral to the job. | 10/26/2019 |
| 13531 | Biotechne Newark, CA Research Associate, Probe Design BS in biological sciences Exp: 0-2 years |
We are seeking a Research Associate Scientist to join the R&D probe design team. The candidate will be responsible for ordering probes for synthesis and updating probe databases as well as other supportive functions. Prepare and send probe sequences to vendors for oligo synthesis. Communicate with internal stakeholders (Sales, Operations, etc) promptly. Prepare various files and upload to internal databases | 10/26/2019 |
| 13532 | Biotechne San Jose, CA QC Technician BS in biological sciences Exp: 1+ years in manufacturing |
This position’s responsibilities include QC testing in the Reagent and Consumables Manufacturing department at ProteinSimple. The primary responsibility will be working with QC and Production teams to schedule and test Maurice and Simple Western consumables in a timely manner.Precise and meticulous observation and recording of all details of the assay, which are not limited to but including: lot numbers, and physical observations of materials | 10/26/2019 |
| 13533 | Biotechne San Jose, CA Manufacturing Laboratory Technician AA or HS Diploma/GED in biotech, chemistry, biology Exp: 1+ years in lab or manufacturing |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Operate and maintain cartridge fabrication process, with good manual dexterity. Document production batch records/travelers, and computer data entry | 10/26/2019 |
| 13534 | Biotechne Minneapolis, MN Advanced Research Associate - Luminex Development MS in biological sciences or engineering Exp: 0-2 years |
The responsibilities of this position are to assist with feasibility, product development, verification, and technical support of immunoassays. Optimize components and performance, develop manufacturing procedures, transfer product/process to production, and perform necessary troubleshooting. Work on problems of moderate scope where analysis of situation or data requires a review of identifiable factors. Perform additional duties as assigned. | 10/26/2019 |
| 13535 | Exsurco Medical Wakeman, OH Assembly Technician HS Diploma/GED Exp: 3 months in factory experience |
Primary role is to perform all forms assembly activities including equipment setup and tear down where required as well as in-process verifications. In addition, this position includes several cross-functional responsibilities comprising Shipping, Receiving, Job Picking, Warehousing and Plant Cleaning and some Maintenance activities. This position also has responsibilities associated with Servicing returned products (disassembly and reassembly, diagnosis and report writing). | 10/26/2019 |
| 13536 | Endo Pharmaceuticals Field, FL Sales Representative - Miami BS/BA Exp: 1 year in business/biopharma/sales |
Accomplishes targeted sales and increases the market share of key (bio) pharmaceutical products. Calls on a select number of high value physicians in a specified geographic area and focuses on establishing durable relationships, effectively delivering product information, and aiding in training. Helps customers develop reliable processes for reimbursement and access. Is comfortable providing information to the entire office staff and has the ability to identify new sales opportunities and leads in their territory. | 10/26/2019 |
| 13537 | Endo Pharmaceuticals Malvern, PA Associate, Regulatory Affairs Operations BS/BA in sciences Exp: 1-3 years in regulatory affairs |
The Associate, Regulatory Affairs Operations is responsible for the preparation and publishing of electronic regulatory documents and submissions and for ensuring these deliverables are compliant with health authority guidelines. This position is also responsible for the archiving of regulatory correspondence, the preparation and submission of Periodic Adverse Events Reports (PADERS), PADER Waivers, and maintenance of databases within the Regulatory Affairs department. Additionally, and as assigned, the incumbent will perform the essential duties and responsibilities related to pre- and post-approval submissions. | 10/26/2019 |
| 13538 | Endo Pharmaceuticals Field, TN Sales Representative - Nashville BS/BA Exp: 1 year in business/biopharma/sales |
Accomplishes targeted sales and increases the market share of key (bio) pharmaceutical products. Calls on a select number of high value physicians in a specified geographic area and focuses on establishing durable relationships, effectively delivering product information, and aiding in training. Helps customers develop reliable processes for reimbursement and access. Is comfortable providing information to the entire office staff and has the ability to identify new sales opportunities and leads in their territory. | 10/26/2019 |
| 13539 | Enzo Biochem Farmingdale, NY Manufacturing Scientist MS in life sciences Exp: 1+ years |
This position is responsible for the planning, implementation, and maintenance of manufacturing methods, processes, and operations for current and new product lines, as well as contributing to the improvement of production capabilities. The Manufacturing Scientist is also responsible for understanding product specifications, troubleshooting technical problems, and implementing process improvements. | 10/26/2019 |
| 13540 | Enzo Biochem Farmingdale, NY Associate Product Manager BS/BA in life sciences Exp: 1-3 years |
This position is responsible for performing market research in support of new strategic marketing programs. The Associate Product Manager will work with scientific staff to ensure technical accuracy of product documentation. The Associate Product Manager is responsible to manage single projects and/or participate on portions of multiple projects. | 10/26/2019 |
| 13541 | Ora Andover, MA Clinical Trial Associate BS Exp: 1+ years |
Assists project managers in clinical conduct of ophthalmic clinical trials. Serves as point of contact for investigator sites and ensures compliance with protocol and overall clinical objectives. As a member of the clinical operations team, relies on instructions and pre-established SOPs to perform the functions of the job while working under supervision of a supervisor or manager. Performs day-to-day activities under the guidance of the clinical project managers. Placement at the CTA I, CTA II or Sr. CTA level will be determined based on the candidate’s qualifications. etc. | 10/22/2019 |
| 13542 | Organogenesis Norwood, MA QC Analyst I - Microbiology BS in microbiology or related Exp: 6 months - 1 year |
The QC Analyst I/II performs quality activities in support of product production and releases. The position has interaction with other internal departments, including Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also has interactions with external entities including contractors and suppliers. The QC Analyst I/II performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, and reporting results. etc. | 10/22/2019 |
| 13543 | OriGene Technologies Rockville, MD Research Associate – Immunology BS/MS in biology, biochemistry, or related Exp: 1-2 years |
Responsibilities: Involves multiple de novo R/D projects for antibodyand assay products development.Performsvalidation tests on variant sera or antibody samples. Participates other duties such as antibody production, purification and conjugation. Strong organizational skills and possess strong ability to identify, analyze and solve the problems independently. Records experiment procedure and results in notebooks and computer accurately. Prepares summary tables, reports, specification datasheets and presentation data on PPT-Maintains laboratory equipmentand a safe working environment. etc. | 10/22/2019 |
| 13544 | OriGene Technologies Rockville, MD Research Associate – Molecular Biology BS in a life science Exp: 1+ years |
The qualified candidate will support company’smolecular biology operations,principally performing DNA cloning and molecular biology experiments following protocols. Job Requirements: Perform experimentsfollowing protocols for plasmid DNA purification, DNA digestion, gel electrophoresis,DNA fragment purification, ligation, transformation, DNA quantitation, DNA sequencing, PCRand cell culture. Responsible for assigned lab duties, maintaining lab stocks, solutions, reagents, and supplies. etc. | 10/22/2019 |
| 13545 | Owl Biomedical Santa Barbara, CA Assembly & Test Technician AS/AA Exp: 1-3 years |
To support this effort, we are seeking an Assembly and Test Technician to support the assembly of designed parts for the company’s core medical instruments. Within this role, you will be responsible for supporting all tasks and functions in producing interposer to chip assemblies, while inspecting incoming raw materials and maintaining inventory for all production parts. Overall, your keen ability to work with a multi-disciplinary team to lead and advance product development efforts will champion the continued success of Owl biomedical. etc. | 10/22/2019 |
| 13546 | Owl Biomedical Sunnyvale, CA Manufacturing Associate BS in a biological science or related Exp: 1-3 years |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. etc. | 10/22/2019 |
| 13547 | Nephron West Columbia, SC Microbiology Analyst I BS in biology, microbiology, or other life science Exp: 1+ years |
Position Summary: Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Demonstrate high proficiency level on tests performed. Additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. Apply quality scientific techniques in the microbiological analysis of raw materials; in-process & finished product samples to include: sterility, bioburden, identification, environmental monitoring, growth promotion, microbial recovery and media fill tests following approved procedures. etc. | 10/21/2019 |
| 13548 | NGM Biopharmaceuticals South San Francisco, CA Research Associate - Nonclinical Safety (Temp to Perm) BS in a life science Exp: 1+ years |
NGM Biopharmaceuticals, Inc. is seeking a highly motivated Research Associate to join our Nonclinical Safety development group. This will be a temp to full time position. | 10/21/2019 |
| 13549 | Nitto Milford, MA Operations Program Associate BS in industrial, chemical, or mechanical engineering Exp: 0-3 years |
Assist in managing a portfolio of strategic projects driven by the organization’s on-going continuous improvement efforts. Analyze and improve complex systems impacting the organization’s performance as it pertains to its customers and key stakeholders. Perform duties as required for major projects throughout the organization. Key Responsiblities: Help manage and interpret data analysis of CI stats. Report periodically to senior management on status and recommend modifications as necessary. Assist with strategic project analysis and modeling to determine the benefit to the organization and its stakeholders. Propose prioritization and resource requirements to management based on this analysis | 10/21/2019 |
| 13550 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior Research Associate MS Exp: 0-3+ years |
We are currently offering a unique opportunity for a highly motivated researcher to join our team with experience in immune, in vitro, cellular and cancer biology. JOB DUTIES AND RESPONSIBILITIES: Execute a broad range of cell based functional and phenotypic assays for characterization of engineered NK and T-cells to accelerate projects in pre-clinical development. Conduct in vitro mechanism of action studies using primary human or mouse immune cells and cell lines to evaluate activity of candidate therapies. etc. | 10/21/2019 |
| 13551 | Nkarta Therapeutics South San Francisco, CA Research Associate (In Vivo) MS in a pharmaceutical or biotechnological field Exp: 1 year |
We are currently offering a unique opportunity for a highly motivated researcher to join our team with experience in immune, in vitro, cellular and cancer biology. JOB DUTIES AND RESPONSIBILITIES: Conducts pharmacological evaluation of test agents (cell products or small molecule) in subcutaneous, systemic and orthotopic in vivo oncology models. Assists in sample processing, homogenization, or generation of single cell suspensions for ex vivo flow cytometry analysis or PCR analysis. Contributes to preclinical research through development or validation of new tumor models. etc. | 10/21/2019 |
| 13552 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior/Process Engineer MS in a biology-related field Exp: 1-6+ years |
We are currently offering a unique opportunity for a highly motivated development associate to join our team with development experience in cell therapy. JOB DUTIES AND RESPONSIBILITIES: Support process development of phase appropriate cell therapy production processes. Evaluate raw materials and culture systems for use in cell therapy manufacturing processes. Support process optimization efforts to increase process robustness, reduce costs and improve yield. etc. | 10/21/2019 |
| 13553 | Noble Life Sciences Woodbine, MD Animal Care Tech BS Exp: 1 year |
The Animal Care Tech is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Vivarium Manager. Responsibilities include but are not limited to: Read, understand and follow all SOP’s, Quality Assurance Standards and perform duties in accordance with the study protocol. Monitor daily animal health and wellness checks and report any abnormal animal conditions to the supervisor and/or the Study Director and record observations in appropriate logs. etc. | 10/21/2019 |
| 13554 | Noble Life Sciences Woodbine, MD Quality Control Associate BS Exp: 1 year |
The QC Associate is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to Sr. Vice President and a Consulting Quality Assurance Unit. Responsibilities include butarenot limited to: Become and maintain intimatefamiliaritywith all applicable FDA and EPA GLPand other appropriate regulations and guidelinesas well as with the company SOPs and other QA systems. Supervise day to day quality control operations and documentation. etc. | 10/21/2019 |
| 13555 | Nordson Minneapolis, MN Product Development Engineer I BS in engineering Exp: 0-3 years |
Applies broad knowledge of principles and practices in Design Engineering. Independently evaluates, selects, and adapts standard techniques, procedures, and criteria. Acquires general knowledge of principles and practices of related fields. Works on multiple projects with low level of oversight from project manager and/or technical lead. Essential Job Duties and Responsibilities: Provide engineering support to the project team to design and develop medical devices (disposable and reusable), catheters, implants, and/or packaging, from concept through market introduction. etc. | 10/21/2019 |
| 13556 | NorthStar Medical Radioisotopes Beloit, WI Process Laboratory Technician BS in chemistry or a related physical science Exp: 1+ years |
Responsible for routine (chemistry) laboratory support in one of NorthStar’s research and development laboratories. This individual will be responsible for maintaining the laboratory space to cGMP standards, creating and documenting standard laboratory solutions, and assisting in the maintenance and calibration of analytical measurement equipment. etc. | 10/21/2019 |
| 13557 | Norwich Pharma Norwich, NY Chemist I BS in chemistry, biology, or related Exp: 0-3 years |
The Quality Control Chemist I: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. etc.The Quality Control Chemist I: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. etc. | 10/21/2019 |
| 13558 | Novo Nordisk West Lebanon, NH Manufacturing Technician Job BS Exp: No experience necessary for BS candidates |
Novo Nordisk in West Lebanon is looking for a Manufacturing Technician to join our team! This position has primary responsibility to support the manufacturing processes and requires strict adherence to established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 10/21/2019 |
| 13559 | Novo Nordisk West Lebanon, NH QC Analyst - Analytical Job BS Exp: 1+ years |
We're looking for a detail oriented QC Analyst I. The ideal candidate will be proficient in method validation and equipment qualification with minimal supervision, as well as performing chemical testing for raw material, water and in-process samples supporting the manufacturing process. Demonstrates self-starter and independent worker with strong commitment in quality and compliance. Excellent analytical and wet chemical techniques. Strong team player with the ability to communicate effectively both verbally and in writing. The person will join our Analytical team to support routine testing such as SDS-PAGE, FTIR, HPLC/UHPLC, ELISA, UV-VIS and others. etc. | 10/21/2019 |
| 13560 | Novozymes Research Triangle Park, NC Research Assoc/Assoc Scientist, Microbial Formulation Dev BS/MS in chemical engineering, biology, chemistry, or related Exp: 0-8 years |
Are you ready for a challenging role that lets you use both your scientific grounding and communication skills? If so, you could be our new colleague in our Formulation Development Group, a dynamic team of scientists and researchers located in RTP, NC. You’ll work within the internal research group, as well as with outside units, to develop advanced and scalable formulations and formulation processes for both existing and novel microbe-based products (i.e. bacteria, fungi and yeast). Alongside an in-depth understanding of the scientific principles of microbial formulation and process development, you demonstrate good stake-holder management and exceptional communication skills. In your daily work, you’ll use all of these talents to pioneer research and transform it into value-added products for a variety of industries, including agriculture, household care and biofuels. etc. | 10/21/2019 |
| 13561 | Nurix San Francisco, CA Research Associate I-II, Cell Biology/Immunology BS/MS Exp: 0-4 years |
We are seeking a Research Associate with experience in cell biology and immunology to join our Nurix drug discovery team. Nurix is devoted to unlocking the therapeutic potential of the ubiquitin system to explore the possibility of modulating targets previously believed to be “undruggable”. Ubiquitin ligases play numerous roles in immune cell function, autoimmunity, inflammation and anti-tumor immunity. The successful candidate will support early drug discovery efforts in inflammation, oncology and immuno-oncology (IO). etc. | 10/21/2019 |
| 13562 | Novavax Gaithersburg, MD Research Associate II (TEMP TO PERM) MS Exp: 1+ years |
We are seeking Research Associate II to join our Clinical Immunology department in Gaithersburg, MD. This individual will play an important role testing clinical samples. Qualified individuals are expected to generate accurate high throughput clinical data. Responsibilities include but are not limited to: Play a key role in performing technical laboratory processes, including training on existing assays and clinical testing related activities as per schedule and under manager discretion in a GxP environment. etc. | 10/21/2019 |
| 13563 | Editas Boulder , CO Research Associate, Medicinal Chemistry Group BS/BA in chemistry Exp: 1 year or more with synethtic organic chemistry |
This new role on the Medicinal Chemistry team in Boulder provides a unique opportunity to contribute to Editas’ efforts through the development of novel chemical compounds to improve CRISPR/Cas9 and CRISPR/Cpf1 performance. Design and synthesize compounds to improve the performance of ribonucleoproteins (CRISPR/Cas9 and CRISPR/Cpf1). Optimize synthetic methods for compounds of interest. | 10/20/2019 |
| 13564 | Editas Cambridge, MA Research Associate I/II, In Vivo Pharmacology BS or MS in biological sciences Exp: 1-2 years lab experience |
The candidate will be responsible for conducting preclinical animal studies to support the development of gene-editing based therapies in multiple disease areas, including ophthalmology, oncology, and hematology. Perform basic molecular biology work such. Perform routine injections (sc, ip, iv) in mice, monitor animal health, collect tissue and blood samples, measure tumor volume, perform anesthesia and necropsies. | 10/20/2019 |
| 13565 | Editas Cambridge, MA Research Associate I/II, Cell Biology BS or MS in biological sciences Exp: 1-3 years lab experience |
In this role you will contribute to the development of cell-based assays and ex vivo methods to evaluate gene editing. An ideal candidate should have a background in cell culture, ex vivo tissue dissection methods, and a strong interest in genome editing. Perform ex vivo tissue dissection and cell isolation. Perform routine DNA/RNA extraction and PCR, western blot, and ELISA. Development and optimization of cell-based assays | 10/20/2019 |
| 13566 | Edwards Irvine, CA Engineer II, Automation & Process mS in Mechanical, Electronic, Mechanics, Mechatronics, Industrial Exp: 0-2 years in automation |
This is a great opportunity to lead and provide support in projects for the manufacturing area. This includes: automation projects for processes of new products, automation projects for cost reduction, quality, ergonomics and delivery improvements. In addition, validation and implementation of changes related to the projects. Develop moderately complex tests and experiments (including writing and execution of protocols) to qualify and validate manufacturing processes; follow up on protocol activities, train technicians; analyze results, make recommendations and develop reports. | 10/20/2019 |
| 13567 | Edwards Irvine, CA Associate Analyst, Inventory BS/BA Exp: 1 year in finance/customer serivce/operation etc. |
Manage all consigned and customer owned inventories through a variety of processes and systems and provides insight to help improve and streamline current processes in collaboration with Commercial Contract, Finance, Sales, Supply Chain and Customer Operations. Perform basic analysis of field scan results (e.g., physical vs system of record inventory) for SOX Compliance through multiple systems, cross functional departments (e.g., Contracts, Sales, Finance, Quality, Implant Registry, Supply Chain, Customer Service, IT) and external partners to make recommendations to customer service for resolution. | 10/20/2019 |
| 13568 | Edwards Irvine, CA Technician, R&D - Transcatheter Heart Valve HS Diploma Exp: 1+ years related experience |
Edwards Lifesciences is currently seeking a Research and Development Technician to perform a wide variety of tasks in support of Engineering activities for our Transcatheter Heart Valve Business Unit at our corporate headquarters in Irvine, CA. Perform set-up on textile and related machines involving mechanical components as well threading of fine textile yarns using mechanical tools . Support engineering activities such as test, check-out, modification, fabrication, and assembly under the close supervision of Engineers | 10/20/2019 |
| 13569 | Edwards Irvine, CA CRA I, In House - Transcatheter Mitral and Tricuspid Therapies BS in related Exp: 1 year in documentation for clinical studies |
This is a unique opportunity to join an early-stage product development group, Transcatheter Mitral & Tricuspid Therapies (TMTT), focused on developing solutions for patients suffering from structural heart disease. The Clinical Research Associate I will ensure clinical trials are conducted and reported in accordance with all applicable regulatory requirements. Conduct reviews of documentation needed for internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations. | 10/20/2019 |
| 13570 | Edwards Draper, UT Quality Engineer I, Quality BS or MS in engineering Exp: 0 years |
Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Optimize Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk. | 10/20/2019 |
| 13571 | Edwards Draper, UT Manufacturing Engineer II - Transcatheter Mitral and Tricuspid Therapies MS in engineering/sciences Exp: 0 years w/internships or senior projects |
Applies knowledge of technical principles and Edwards systems/procedures to optimize manufacturing processes. Improve manufacturing processes using engineering methods (e.g., LEAN methods, basic statistics) for continuous process improvement. Develop basic experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports. Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes. | 10/20/2019 |
| 13572 | Edwards Draper, UT Supplier Quality Engineer I BS in engineering/sciences Exp: 1-2 years in medical devices |
Edwards Lifesciences has an exceptional opportunity for an Engineer I within the Supplier Quality group. This person will be responsible for supporting supplier quality vendor management, audits, and improvements while supporting continued Quality System improvements. In this position you will support activities sustaining quality engineering within Receiving Inspection, Manufacturing, and Product Verification as applied to supplier related issues. | 10/20/2019 |
| 13573 | Elanco Greenfield, IN Associate-Advanced Analytics BS in finance/statistics or data Exp: 1 year in data analytics |
Creates, grows and maintains relationships with internal customer groups to facilitate data driven decisions on business critical projects. Key customer groups to consist of Marketing, Finance, Sales, Senior Leaders, Corporate Strategy and Supply. Responsibilities for providing ROI, efficiency and sales lift metrics to customer groups in a form that both drives decisions to spend and optimizes efficiency. Supports the creation of financial business cases and provides predicted outcomes that can be measures in subsequent ROI and efficiency reviews. | 10/20/2019 |
| 13574 | Elanco Winslow, ME Biologist - QC MS in biological sciences Exp: 0-3 years lab experience |
The Biologist-QC will provide technical support including consultation/recommendation on various analytical topics to management where appropriate. He or she will support and sometimes manage laboratory related projects affecting QC. The Biologist will assist other laboratory personnel in the implementation of new technologies into the QC lab and improvement of existing processes. The Biologist will also coordinate non-routine analytic work and sample analysis to support relevant projects and initiatives when needed. The position will also include routine testing of in process and final product samples for the release of veterinary vaccines. | 10/20/2019 |
| 13575 | Lilly Charlottetown, Pr Production Technician - Fermentation BS/BA in life sciences Exp: 1-2 years in GMP bio manufacturing |
To produce veterinary biologics according to a defined production schedule following cGMP guidelines and specific outlines of production to meet market demands for Aquaculture products. Comply with safety requirements, cGMP, SOP and manufacturing documentation. Produce antigens in a timely manner according to their approved Outline of Production/Product Dossiers and to cGMP guidelines. Support Antigen production and freeze dried vaccines production according to Standard Operating Procedures and Protocols. | 10/20/2019 |
| 13576 | Lilly Indianapolis, IN Engineer-Automation-IDAP BS in engineering or computer science Exp: 0-3 years |
Develop, implement, and continuously improve process automation solutions within IDAP to ensure that business goals are achieved. Ensure that process automation solutions/systems are in-control, capable, and compliant. Stay tightly aligned and actively involved with internal customers. Understand their issues, priorities and objectives. Respond to and implement customer requests. Troubleshoot problems. Assure that all capital projects are aligned with the Automation Strategy and that all established standards are followed. | 10/20/2019 |
| 13577 | Element Science San Francisco, CA Product Test Engineer BS in electrical engineering Exp: 0-2 years |
The Product Test Engineer is responsible for the co-development and maintenance of all production test equipment and software. Your role is critical as it takes a candidate that understands all the stages of test development to ensure our products are built correctly and ready as a Class III bio-medical device. You will work directly with product design engineers and use your production-level test knowledge to create effective test sequences, supporting hardware and software, and overall record keeping strategy. | 10/20/2019 |
| 13578 | Lilly Columbus, OH Entry-Level Sales Representative-Ohio Valley Area Diabetes Primary Care (OH/MI/IN/KY) BS/BA Exp: license/certification for position |
Partner with health care professionals and those involved with patient care as a product expert to tailor solutions for patient therapy. Sell in a changing health care environment, utilizing critical thinking and a strategic mindset to understand the environment (payer, health systems, business) and gain access to the customers to make an impact on patients’ lives. Work in your own territory and also partner with team members and alliance partners for success in the territory | 10/20/2019 |
| 13579 | Emerald Cloud Lab South San Francisco, CA Laboratory Operator II HS Diploma/BS/BA Exp: 1-3 years in life sciencesz |
As a Laboratory Operator II, you will be responsible for high fidelity execution of detailed protocols. Operators are relied on for the immediacy and reliability with which experiments are run on the ECL, so attention to detail is crucial. The Lab Ops team relentlessly clears the queue of customer experiments and keeps the robots in the labs running at all times, with a focus on exactness and increasing efficiency. The entire ECL facility is run in a systematic way, and the team purview encompasses all protocols that enable this, from maintenance and control of instruments to inventory intake. | 10/20/2019 |
| 13580 | Emergent Biosolutions Camden, MD Packaging & Inspection Technician HS Diploma Exp: 0-2 years |
This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. Execute and document procedural steps in compliance with cGMP standards. Perform room clearances in accordance with relevant Standard Operating Procedures. Perform 100% visual inspection of product and classify rejected materials utilizing approved categories within required timelines (Qualification) | 10/20/2019 |
| 13581 | Lilly Harrisburg, DE Entry-Level Sales Representative-Mid Atlantic Area Diabetes Primary Care (PA/MD/VA/DC) BS/BA Exp: license/certification for position |
Partner with health care professionals and those involved with patient care as a product expert to tailor solutions for patient therapy. Sell in a changing health care environment, utilizing critical thinking and a strategic mindset to understand the environment (payer, health systems, business) and gain access to the customers to make an impact on patients’ lives. Work in your own territory and also partner with team members and alliance partners for success in the territory | 10/20/2019 |
| 13582 | Lilly Greenfield, IN Associate-Advanced Analytics BS in finance/statistics or data Exp: 1 year in data analytics |
As part of the Global Commercial Analytics, this position will support Elanco’s US and Top International markets with a focus on Advanced Analytics to drive data driven decisions and make Elanco the “Best Run Animal Health Company”. To meet role requirements, candidates must have an understanding of analytical modeling techniques and software, the animal health industry and data visualization approaches to drive insights to actions. | 10/20/2019 |
| 13583 | Editas Cambridge, MA Research Associate I/II, Biological Development BS or MS in biological sciences Exp: 1-2 years lab experience |
The candidate will be responsible for conducting preclinical animal studies to support the development of gene-editing based therapies in multiple disease areas, including ophthalmology, oncology, and hematology. Perform basic molecular biology work such as DNA and RNA extraction, qPCR, western blot, and ELISA. Perform post-in vivo experiments collect tissue and blood samples and process samples for downstream assays. | 10/20/2019 |
| 13584 | Cytokinetics South San Francisco, CA Research Associate I, Pharmacology BS/MS in biology, physiology, pharmacology Exp: 1-3 years |
This individual will also be involved in managing transgenic mouse colonies, maintaining transgenic lines for experimental purposes and designing, optimizing, and implementing new assays to measure cardiovascular system function. As a member of a multidisciplinary team, you will work closely with team members to identify, characterize and advance compounds through research and preclinical development. | 10/19/2019 |
| 13585 | Cytokinetics South San Francisco, CA Research Associate, Sample Management BS in chemistry Exp: 0-3 years lab experience |
This will be an entry level position that will provide a tremendous learning opportunity for the ideal candidate. The candidate will get to learn in-depth the functioning and nuances of a Sample Management group and also gain experience with the numerous assays that assess and characterize the properties of the compounds. The position demands an individual who is a quick learner and has a proactive attitude to pitch in to support research activities and help with dispensing compounds, trouble-shooting instrumentation, and running assays. | 10/19/2019 |
| 13586 | CytomX Therapeutics South San Francisco, CA Research Associate I/II: Upstream Process Development BS or MS in biological sciences Exp: 0-3 years lab experience |
Operation, harvest, and cleaning of stirred-tank bioreactors (AMBR15, 2-20L glass vessels, 50 L SUB, fed-batch). Media and reagent preparation to support upstream activities. Execute and evaluate of fed-batch cell culture studies in shake flasks and micro-bioreactors. Execute and evaluate of fed-batch cell culture studies in shake flasks and micro-bioreactors. Support of GMP mfg; may include BPR review and PIP duties | 10/19/2019 |
| 13587 | Cytovance Biologics Oklahoma City, OK DOWNSTREAM MANUFACTURING ASSOCIATE AS/AA in sciences or chemical engineering Exp: 0-2 years GMP production |
This position is accountable for the execution of procedures for purification manufacturing and support area of manufacturing using SOP’s and batch records. Operating production equipment for purification that may include process monitoring, purification and formulation. Interface with Quality Control department to submit in-process samples and coordinate environmental monitoring during key process steps. Demonstrate understanding in scientific concepts, technical operations, safety, and Good Manufacturing Practice. | 10/19/2019 |
| 13588 | Cytovance Biologics Oklahoma City, OK UPSTREAM MANUFACTURING ASSOCIATE AS/AA in science or biotech Exp: 1-2 years in GMP |
Executes upstream manufacturing of clinical and commercial products. Executes pre and post processing activities such as: clean of production equipment, including the operation of automated bioreactor, harvest and media prep skids. This position is accountable for executing the manufacturing processes in Contract Manufacturing Facility and/or Master Cell Banking Facility. | 10/19/2019 |
| 13589 | Cytovance Biologics Oklahoma City, OK SOLUTION PREP ASSOCIATE I AS/AA in science or biotech Exp: 1-2 years in GMP |
This position is accountable for producing and delivering large and small-scale media and buffers to support Upstream and Downstream Manufacturing Operations. Batching and delivering both large and small-scale media and buffer batches. Assisting in the review & creation of operation documents by providing input to technical composition of documents. Following accurate oral & written procedures in operating production equipment & performing processing steps | 10/19/2019 |
| 13590 | Dexcom Mesa, AZ Process Technician 1 BS/BA Exp: 0-2 years |
Performs research and/or development in collaboration with others to complete science-based projects. Makes detailed observations, analyzes data and interprets results. Investigates, creates and develops new methods and technologies for project advancement. Maintains high level of professional expertise through familiarity with scientific literature. May participate in scientific conferences and contribute to scientific journals. May be responsible for identifying patentable inventions. May act as principal investigator in conducting own experiments. | 10/19/2019 |
| 13591 | Dexcom San Diego, CA Mechanical Engineer 1 BS in technical degree Exp: 0-2 years |
As a member of the R&D Mechanical Engineering team this engineer will understand and articulate the current and future needs of our customers and our business, explore and evaluate new technologies and concepts for meeting those needs, and rapidly demonstrate feasibility of such technologies through rigorous modeling, analysis, prototyping, experimentation, and other risk identification and mitigation activities. Design, develop, fabricate, assemble and implement fixtures and equipment to quantify prototype device performance | 10/19/2019 |
| 13592 | Dexcom San Diego, CA Process Development Engineer 2 MS in technical discipline Exp: 0-2 years |
Develops new or modified process formulations, defines processing or handling equipment requirements and specifications, and reviews processing techniques and methods applied in the manufacture, fabrication, and evaluation of products. Involvement may begin at any step from pilot plant to full-scale manufacturing. Coordinates design requirement review with appropriate engineering/scientific personnel to ensure compatibility of processing methods. Compiles and evaluates test data to determine appropriate limits and variables for process or material specifications. May conceive and plan projects involving definition and selection of new concepts, equipment automation technology, and approaches in the processing or development of new or improved processes. | 10/19/2019 |
| 13593 | Dexcom Mesa, AZ Manufacturing Clerk 1 HS Diploma Exp: 0-2 years related |
Provides administrative and clerical support specifically related to manufacturing department activities. May be assigned to various administrative tasks within manufacturing support. Basic understanding of general job aspects and limited understanding of the detailed aspects of the job. Acquires job skills and learns the policies and procedures required to complete routine tasks. | 10/19/2019 |
| 13594 | Dexcom San Diego, CA Process Development Engineer 2 (Vision System) MS in technical discipline Exp: 0-2 years |
Supports development of new and modified sensor manufacturing processes. Assist lead engineers in defining processing or handling equipment requirements and specifications, and reviews processing techniques for manufacture of new products and to decrease cost, improve throughput, and improve overall quality for commercial product lines. Support transfer and work on process development/scale up or new products from R&D. Manufacturing support to identify and resolve technical issues. Involvement may begin from feasibility at vendors to full scale manufacturing. | 10/19/2019 |
| 13595 | DNA Diagnostics Center Fairfiedl, OH Rep I, Client Services Representative HS Diploma Exp: 1-2 years in customer service |
The Rep !, Client Services Representative is a critical position in providing customer service satisfaction and representing DNA Diagnostics Center (DDC). Answer inbound telephone and email contacts. Able to explain and promote DDC's products and services professionally. Quickly understand and analyze customer needs, listen actively | 10/19/2019 |
| 13596 | DSG San Diego, CA Business Development - San Diego, CA BS/BA in life sciences, business or computer sciences Exp: 1-3 years project management/internship experience |
The Business Development Manager is responsible for identifying new clients and for establishing and maintaining sales relationships. This candidate is also responsible for maintaining and strengthening relationships with existing clients. As a successful candidate, you will need to meet the following technical requirements and qualifications: Place outbound calls to market to qualify and build relationships with contacts, and secure meetings. Educate prospects on the eCaseLink suite of products and services. | 10/19/2019 |
| 13597 | DSG Raliegh, NC Business Development - Raliegh BS/BA in life sciences, business or computer sciences Exp: 1-3 years project management/internship experience |
The Business Development Manager is responsible for identifying new clients and for establishing and maintaining sales relationships. This candidate is also responsible for maintaining and strengthening relationships with existing clients. As a successful candidate, you will need to meet the following technical requirements and qualifications: Place outbound calls to market to qualify and build relationships with contacts, and secure meetings. Educate prospects on the eCaseLink suite of products and services. | 10/19/2019 |
| 13598 | Durect Cupertino, CA Operations Administrative Assistant HS Diploma Exp: 0-1 years in admin |
Provide operational support to multiple functional departments; Facility, Finance, IT, QA, BD, PSRD, and Legal to contribute to the development and implementation of organization goals. Coordinate department, project ,and, business development client meetings and webinars, related luncheons, prepare and distribute meeting documentation. Schedule and coordinate with external vendors, i.e. Facilities and Manufacturing, for service requests | 10/19/2019 |
| 13599 | Dynosense San Jose, CA QA Engineer BS in computer science, engineering or related Exp: 0-2 years |
Develop test plan, test cases, test scenarios based on Users Stories and product’s design description to meet business requirements and technical specifications. Estimate, plan, and coordinate testing activities. Perform ad hoc, functional, integration, and regression testing. Identify software defects and submit problem reports via bug-tracking system | 10/19/2019 |
| 13600 | Nanolab Technologies Milpitas, CA Sample Prep Technician BS/BA in engineering/physical sciences Exp: 0-2 years in FIB/SEM operations |
Nanolab Technologies is looking for an enthusiastic TEM Sample Preparation Technician. Primary function is processing/imaging STEM/TEM samples using FEI 4xx/Helios Dual Bean FIB tools and TEM sample preparation of lamella. The work environment is fast-paced with firm deadlines. The successful candidate will work as a part of a team and be expected to rapidly gain a working knowledge of many analytical techniques. | 10/19/2019 |
| 13601 | Dendreon Union City, GA Quality Specialist, Training BS/BA in science, education or related Exp: 1-3 years in quality/compliance/training, etc |
The primary role of the Quality Specialist I, Training will be to provide training support/ownership for the organization which includes tracking, reporting, executing, and building within the Learning Management System (LMS). These activities aid in remaining compliant to all applicable governing requirements/regulations. Provide LMS training and support to the organization which includes general cGMP training, on the job training, and environmental health and safety training | 10/19/2019 |
| 13602 | Dexcom San Diego, CA Clinical Research Associate MS in technical discipline Exp: 0-2 years |
Able to work independently to implement and monitor clinical studies at participating study sites according to FDA’s Code of Federal Regulations (CFR), Good Clinical Practices (GCP), and ICH Guidelines. Works with Clinical Affairs management to plan and execute the design and conduct of Dexcom-sponsored studies (including In-House studies). Responsible for overall study planning and ensuring that all site visits, monitoring, data collection, reports, and ancillary requirements are appropriately assigned and executed to meet company deadlines, quality expectations, and priorities. | 10/19/2019 |
| 13603 | Dexcom San Diego, CA Firmware Engineer 2 MS in technical discipline Exp: 0-2 years |
Learn and design protocols for continuous glucose monitoring systems. Design, implement and test firmware solutions. Within a team, execute projects for on-time delivery of project objectives. Contribute to and review technical solutions for product integration. Create and execute software design verification protocols. Identify and implement engineering and quality process improvements | 10/19/2019 |
| 13604 | Covance Greenfield, IN Study Technician - Dose Formulations BS/BA in life sciences Exp: 0-2 years |
The Study Technician is a true laboratory position where you collect and document study data step by step. You will perform study calculations and specific techniques for test material formulation. In addition you will: Prepare laboratory reagents, vehicles, diets, solution/suspensions, and capsules. Perform study calculations and specific techniques for test material formulation. | 10/16/2019 |
| 13605 | Covance Dallas, TX Research Technician (On-call) BS, AS/AA or HS Diploma/GED Exp: AS/AA: 1 year clinical research experience, HS: 1-2 years |
Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings. Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples. Assist in the preparation of rooms and medical equipment. Transcription of data from source documentation onto the Case Report Forms (CRFs) for simple to complex studies and QC of CRFs. | 10/16/2019 |
| 13606 | Covance Madison, WI Research Assistant I (Chemist) – Dose Analysis BS/BA in chemistry or related Exp: 1-2 years lab experience |
In this role, you will analyze biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. Organizes and conducts routine analyses in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines. Sets up, operates and performs routine and non-routine maintenance on general equipment. | 10/16/2019 |
| 13607 | Covance Somerset, NJ Animal Technician-Large Animal Toxicology BS/BA Exp: 0-4 years |
The Animal Technician provides primary care to the animals in the large animal toxicology department and performs routine invasive and non-invasive technical procedures on studies allocated to the team while ensuring that procedures are conducted according to protocol, SOP requirements, Good Laboratory Practice (GLP) and United States Department of Agriculture (USDA) regulations and the guidelines. | 10/16/2019 |
| 13608 | Covance Madison, WI Research Nurse , Phase I Clinical Research Unit BSN/AND in WI Exp: 1+ years nursing experience |
Our Clinical Research Unit in Madison, Wisconsin is seeking Research Nurses to join our expanding team. As a Research Nurse at Covance you will be responsible for study unit activities in the conduct of clinical trials with emphasis on the safety and welfare of study participants. | 10/16/2019 |
| 13609 | Covance Dallas, TX Research Technician (On-call) BS, AS/AA, or HS Diploma Exp: BS: 0 years, AS/AA: 1 year, HS: 1-2 years |
Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings. Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples. Assist in the preparation of rooms and medical equipment. Transcription of data from source documentation onto the Case Report Forms (CRFs) for simple to complex studies and QC of CRFs. | 10/16/2019 |
| 13610 | CSBio Milpitas, CA Technician, R&D BS/BA in chemistry, biochemistry ,or related Exp: No experience required |
Perform peptide related lab operation under close supervision. Assist in setting up and operating peptide related lab equipment. Perform HPLC, mass spectrometry, and other analytical techniques. Follow standard operating procedures (SOP) to perform various laboratory tasks. Complete training and development on an ongoing basis | 10/16/2019 |
| 13611 | CSL Lansing, MI Phlebotomist HS Diploma Exp: 12 montsh in medical/health care |
Responsible for the efficient and effective collection of plasma by performing venipuncture, monitoring the pheresis process and following Standard Operating Procedures (SOPs). In compliance with SOPs, performs all aspects of the pheresis procedure and plasma collection, including donor set-up, donor monitoring and donor disconnect. Evaluates vein performance of the donor to identify possible problems; makes necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments when necessary to make the process a positive experience for the donor. | 10/16/2019 |
| 13612 | CSL South Portland, ME Quality Specialist Associate/Bachelors in business admin or biological sciences Exp: 1 year in leadership/regulated environment |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 10/16/2019 |
| 13613 | CSL Smyrna, GA Quality Specialist Associate/Bachelors in business admin or biological sciences Exp: 1 year in leadership/regulated environment |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 10/16/2019 |
| 13614 | CSL Holly Springs, NC Technician I/ II (Calibration) Day Shift HS Diploma or AS/AA Exp: HS: 1 year, AS/AA: 0 years |
Provides calibration and instrumentation support for processes, operations, and buildings on site. Responsible to execute scheduled calibrations, preventive maintenance and corrective maintenance on instrumentation and control devices in compliance with facility procedures and work instructions. Works within clearly defined standard operating procedures and/or scientific methods and adheres to quality guidelines | 10/16/2019 |
| 13615 | CSL Palm Bay, FL Quality Specialist Associate/Bachelors in business admin or biological sciences Exp: 1 year in leadership/regulated environment |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 10/16/2019 |
| 13616 | CSL Las Vegas, NV Customer Service - Donor Support Technician HS Diploma/GED Exp: 3 months |
Responsible for preparing the donor, donor area and equipment for the pheresis process. Monitors the donor and the pheresis process, responds to specific alarms or signals that may occur during the process. Maintains alertness and awareness to any reaction donor may have during or after the pheresis process and notifies appropriate staff.Uses Personal Digital Assistant (PDA) to record incidents that occur during the pheresis process, such as machine alerts and alarms, volume variances and donor adverse events. | 10/16/2019 |
| 13617 | CSL Raleigh, NC Plasma Processing Technician HS Diploma/GED Exp: 3 months related |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. | 10/16/2019 |
| 13618 | CTI Covington, KY Clinical Safety Scientist I BS, or RN Exp: 1-2 years in GCP |
The Clinical Safety Scientist I is responsible for managing serious adverse events (SAEs) in clinical trials or post-marketing programs, focusing on all aspects of the collection, processing, evaluating and reporting of cases in accordance with CTI’s Global Drug Safety and Pharmacovigilance processes, International Council for Harmonisation (ICH) guidelines, Good Clinical Practices (GCP), applicable regulatory guidelines and study procedures. This individual will track cases from receipt to closure, perform verification of safety data, and will utilize clinical / pharmacovigilance judgment in coding of serious events and synthesizing complex clinical information into accurate and complete narratives. | 10/16/2019 |
| 13619 | CTI Covington, KY Clinical Safety Scientist I BS, or RN Exp: 1-2 years in GCP |
The Clinical Safety Scientist I is responsible for managing serious adverse events (SAEs) in clinical trials or post-marketing programs, focusing on all aspects of the collection, processing, evaluating and reporting of cases in accordance with CTI’s Global Drug Safety and Pharmacovigilance processes, International Council for Harmonisation (ICH) guidelines, Good Clinical Practices (GCP), applicable regulatory guidelines and study procedures. This individual will track cases from receipt to closure, perform verification of safety data, and will utilize clinical / pharmacovigilance judgment in coding of serious events and synthesizing complex clinical information into accurate and complete narratives. | 10/16/2019 |
| 13620 | Azurity Greenwood Village, CO Inside Sales Support 2 year college degree Exp: 1+ years in call center |
To increase product awareness through telemarketing and account support with pharmacies to help achieve company sales targets and improve profitability. To provide communication to key stakeholders for the field sales team to generate new business and maintain current business. Interact with pharmacies by use of appropriate questioning, clarification and language to build effective relationships to increase sales. To speak positively and enthusiastically about the company and its products to ensure that a professional company and brand image is provided at all times. | 10/16/2019 |
| 13621 | Covance Greenfield, IN Medical Technologist I BS/BA Exp: 12 months training in medical technology/experience |
Duties include but not limited to performing established procedures for non-clinical testing as required in all assigned laboratory disciplines. Responsible for analyzing animal specimens with report findings shared with pharmaceutical company. Document and resolve any specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved. | 10/16/2019 |
| 13622 | CTK Biotech San Diego, CA Research Associate BS in biology, immunology, biological sciences Exp: 0-3 years lab experience |
The candidate will function as an integral member of the research/production team to support developmental/production activities in the IVD department. Primary responsibilities include but are not limited to: Assist with study protocol development. Execution and interpretation of experiments. Perform data analysis and present scientific data. Function as a team resource to perform a variety of tests. | 10/16/2019 |
| 13623 | Myriad Mason, OH Biostatiscian MS in statistics Exp: 1+ years |
The Biostatistician will provide statistical leadership in design, analysis, interpretation, and reporting of clinical trials and perform predictive modeling of a wide range of data including clinical, pharmacy claims data, electronic health records (EHR), and pharmacogenomics data that help build the business. The position will be supporting Myriad Neuroscience and based in Mason, Ohio. etc. | 10/15/2019 |
| 13624 | Myriad Salt Lake City, UT Process Technician MS in a chemical, physical, or biological science Exp: 6 months |
The Process Tech III supports the clinical diagnostic lab by troubleshooting process failures, identifying and participating in continuous improvement projects in conjunction with staff and Technical Development, and participating on cross-functional teams to implement new processes into operations. This position will work with department management and quality team members to ensure that appropriate root cause is identified, corrective actions are implemented and proactive process improvements are identified. As directed by management, this role may also support Reagent Manufacturing processes, provided they are maintaining ongoing competency to perform those duties. etc. | 10/15/2019 |
| 13625 | NAMSA St. Louis Park, MN Administrative Assistant AS/AA in a business field Exp: 1-3 years |
Part time. Receives and directs calls, visitors, vendors, service personnel, and all paperwork in a confidential manner. Provides clerical and administrative assistance to leadership and teams. Maintains effective working relationships with co-workers, vendors and clients. Schedules appointments and travel arrangements, as requested. etc. | 10/15/2019 |
| 13626 | NAMSA Northwood, OH Associate Microbiologist BS/BA Exp: 1 year |
Independently perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs, and according to applicable work instructions. Prepare or participate in the preparation of test specifications in conjunction with the requirements of the applicable standards and/or client instructions. May have direct client contact as needed. Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and for taking all concerns to management as required. Accurately collects and records raw data in logbooks and on worksheets. etc. | 10/15/2019 |
| 13627 | NAMSA Northwood, OH Chemist MS Exp: None needed |
Principal Duties and Responsibilities. Independently conduct testing according to written instructions. May be requested to conduct more involved studies. May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. May conduct routine testing per NAMSA SOPs as well feasibility, protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP, etc. Works with management to ensure large studies are completed on or before the due date. Prepare and maintain the reagents required for testing. etc. | 10/15/2019 |
| 13628 | NanoString Seattle, WA Clinical Trial Assistant BS/BA Exp: 1+ years |
The Clinical Trial Assistant (CTA) is primarily responsible for supporting the clinical team. The CTA will manage coordination of activities and ensure timely flow of information to and from the team. S/he handles details of a highly confidential and critical nature, and must function efficiently and effectively in a fast-paced professional environment. S/he will have a proven ability to independently prioritize and manage multiple tasks and projects with competing priorities and deadlines, screen and prioritize communications and opportunities from external sources. etc. | 10/15/2019 |
| 13629 | NanoString Seattle, WA Manufacturing Research Associate I/II BS in molecular biology, biochemistry, or related Exp: 0-2 years |
The Manufacturing Research Associate I/II, CodeSet Manufacturing is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. etc. | 10/15/2019 |
| 13630 | Natera San Carlos, CA Clinical Data Operator I HS diploma or equivalent Exp: 0-1 years |
Natera is currently seeking a Clinical Data Operator to join the operations team. This position accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. PRIMARY RESPONSIBILITIES: Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning. Accession samples with high accuracy and efficiency. Accurately enter patient data into the Laboratory Inventory Management System (LIMS). Ensure that the information in LIMS is up-to-date. Scan test requisition forms and attached paperwork. Ensure that all paperwork belong to patient and upload to case. etc. | 10/15/2019 |
| 13631 | Natera San Carlos, CA Clinical Data Operator I (5:30 -10:30 pm) HS diploma or equivalent Exp: 0-1 years |
Natera is currently seeking a Clinical Data Operator to join the operations team. This position accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. PRIMARY RESPONSIBILITIES: Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning. Accession samples with high accuracy and efficiency. Accurately enter patient data into the Laboratory Inventory Management System (LIMS). Ensure that the information in LIMS is up-to-date. Scan test requisition forms and attached paperwork. Ensure that all paperwork belong to patient and upload to case. etc. | 10/15/2019 |
| 13632 | Natera Austin, TX Clinical Laboratory Operator I BS/BA in a biological science or related field Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: Assist in testing of patient samples according to standard operating procedure. Meet expected performance metrics within role as applicable. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Provide guidance for new team members. Follows GLP (good laboratory practice): maintain clean and organized workspace. Completes training and other deadlines on time. etc. | 10/15/2019 |
| 13633 | Natera Austin, TX Medical Laboratory Scientist I BS/BA in medical technology, biological sciences, or related Exp: 1-2 years |
Natera is currently seeking a licensed Medical Laboratory Scientist to analyze specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: Verify the proper specimen being analyzed and perform tests that need to be completed. Proficient at analyzing clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Provides general oversight of personnel and the daily operations in the lab. Meet expected performance metrics within role as applicable. etc. | 10/15/2019 |
| 13634 | Natera San Carlos, CA Clinical Laboratory Associate I (Temporary) BS/BA in a biological science or related field Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate I (Temporary) to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. PRIMARY RESPONSIBILITIES: Assists in testing of patient samples according to standard operating procedure in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Follows GLP (good laboratory practice): maintain cleans and organized work space. etc. | 10/15/2019 |
| 13635 | Natera San Carlos, CA Clinical Laboratory Scientist I BS/BA in medical technology, biological sciences, or related Exp: 1-2 years |
Analyzes specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: Verify the proper specimen being analyzed and perform tests that need to be completed. Proficient at analyzing clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Follows GLP (good laboratory practice): maintain clean and organized workspace. Completes training and other deadlines on time. etc. | 10/15/2019 |
| 13636 | Natera San Carlos, CA Clinical Laboratory Scientist II BS/BA in medical technology, biological sciences, or related Exp: 1-2 years |
Natera is currently seeking a licensed Clinical Laboratory Scientist I to analyze clinical laboratory specimens following the standard methods and procedures. Maintain equipment and instruments in good operating condition, recognize any malfunctions and troubleshoot as needed. PRIMARY RESPONSIBILITIES: Verify the proper specimen being analyzed and perform tests that need to be completed. Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Follows GLP (good laboratory practice): maintain clean and organized work space. etc. | 10/15/2019 |
| 13637 | NatureWorks Blair, NE Production Technician HS diploma/AA/AS Exp: 1-2 years |
The Production Technician is responsible for the safe execution of the day to day operations of the production plant. This position will work closely with other team members and be responsible for personal and plant safety, environmental compliance, commitment to continuous improvement in the quality of our product, cost control efforts and efficient operations of the plant. This position requires working 12 hour shifts including evenings, weekends and holidays. etc. | 10/15/2019 |
| 13638 | NeoGenomics Aliso Viejo, CA Accessioning Technician I HS diploma/AS/BS Exp: 1+ years |
As an Accessioning Technician I you will ensure proper handling of all specimens received and prepare specimens for laboratory testing. You will be performing functions such as matching patient information, data entry, and scanning documents. You will be responsible for reviewing all requisitions for missing information, working closely with Customer Care in order to obtain missing information in a timely fashion, and distributing new information to all departments involved. You will need to report problem holds and provide resolution in a timely fashion. etc. | 10/15/2019 |
| 13639 | NeoGenomics Aliso Viejo, CA Histotechnician I Nights HS diploma/AS/BS Exp: 1+ years |
As a Histotechnician I you will work under the direct supervision of a licensed physician or surgeon, or within a training environment. You will assist with responsibilities associated with processing specimens for clinical testing and providing general support for the laboratory following established policies and procedures. Receive, organize and process clinical specimens accurately; identify worksheet, computer, and specimen problems and demonstrate ability to either resolve or elevate to licensed personnel appropriately. Prepare and organize written data, printouts, and other documents for pathologist review. etc. | 10/15/2019 |
| 13640 | NeoGenomics Fort Myers, FL Histotechnologist I AS Exp: 1+ years |
As a Histotechnologist I or II, you will work under general direction to precisely and accurately conduct a variety of routine and specialized histology procedures. You will research, troubleshoot, and resolve histology related inquiries and problems within the laboratory. This position requires you to produce the highest quality of embedding, microtomy, tissue grossing, tissue processing, and H&E staining, special staining, immunohistochemistry staining and equipment maintenance. etc. | 10/15/2019 |
| 13641 | Nanosyn Santa Clara, CA Associate Scientist / Analytical Chemistry BS/MS in chemistry or related Exp: 1+ years |
Nanosyn is currently seeking a highly motivated candidate to join the analytical and compounds management team in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of characterization, purification, QC, data processing, etc. for Nanosyn’s chemistry/biology services. She/he will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have at least 1 year of relevant experience, very strong organizational skills, the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. etc. | 10/15/2019 |
| 13642 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in biology, biochemistry, or related Exp: 0-2 years |
We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. etc. | 10/15/2019 |
| 13643 | NanoString Seattle, WA Automation Engineer I/II BS in a science or engineering discipline Exp: 1+ years |
The Automation Engineer I/II is responsible for maintaining existing Manufacturing systems as required. Additional duties include the development of new methods and implementation of new systems. The ideal candidate has knowledge of FDA and ISO requirements as they apply to manufacturing processes. Essential Duties: Maintain/Support Liquid Handling Equipment (Hamilton Star Workstations). Maintain/support customer/build in-house equipment. Support demand label printing system. etc. | 10/15/2019 |
| 13644 | Nelson Labs Salt Lake City, UT Development Chemist BS in chemistry or related Exp: 1-3 years |
Looking for a Development Chemist position with a wide range of experience to work in a fast paced environment. This position involves decision making in the areas of analytical chemistry, equipment maintenance, data quality, and workflow. Duties include analysis of a wide variety of samples following establish methods or standards, and supporting the development and implementation of laboratory policies and procedures. Experience with instrumentation/equipment and software, such as gas chromatography/mass spectroscopy (GC/MS), high performance liquid chromatography/mass spectroscopy (HPLC/MS), and Inductively coupled plasma/mass spectrometry (ICP/MS). etc. | 10/15/2019 |
| 13645 | Nelson Labs Salt Lake City, UT Chemistry Lab Analyst II BS in chemistry or related Exp: 1-3 years |
The Chemistry Laboratory Analyst II conducts testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. etc. | 10/15/2019 |
| 13646 | Cook Medical Bloomington, IN Quality Engineer, Non-Conformance BS in engineering or life sciences Exp: Entry Level |
The Quality Engineer, Non-Conformance at Cook Incorporated serves as the quality representative of certain product lines within product development, manufacturing, post-market surveillance, and/or CAPA. Interface with internal and external groups on quality-related issues. Perform investigation of product non-conformances and/or processes. | 10/13/2019 |
| 13647 | Cook Medical Bloomington, IN Application Engineer BS/BA in computer science or related Exp: Entry Level |
The Application Engineer at Cook Medical configures, implements and documents applications that provide the technical solutions to meet specifications and business requirements defined by company objectives to promote effective, efficient, and compliant operations. Technical responsibility for all stages of solution configuration to ensure compliance with application standards, architectural standards, and achievement of documented requirements. Ensure the stability, integrity and efficient operation of the business/workflow rules that supports core integration functions. | 10/13/2019 |
| 13648 | Cook Medical Bloomington, IN Manufacturing Engineer BS/BA in related field Exp: No experience required |
Responsible for providing technical support for the day-today production activities in the manufacture of custom, plastic components used in the assemblies of various medical devices. This is a hands-on position with visibility on the manufacturing floor and requires a high level of interaction with the production, product development, and quality teams. The engineer is responsible for supporting product development activities, continuous improvement, complaint resolution, CAPA investigations and other quality initiatives. | 10/13/2019 |
| 13649 | Cardinal Health Reno , NV Assoc I, Assembly - Shift (6am - 6pm) HS Diploma/GED Exp: 0-6 months |
Performs a variety of tasks ranging from repetitive to non-repetitive production to put together component parts to make assemblies, sub-assemblies or completed units, using standard operating procedures. May conduct quality inspections on processing line in accordance with quality specifications. | 10/13/2019 |
| 13650 | Cardinal Health Reno , NV Associate II, Warehouse Ops HS Diploma/GED Exp: 1-2 years |
Warehouse Operations is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. Also responsible for the efficient flow of products from the point of product receipt from vendors to the shipment of products (via prescribed service parameters) to a variety of internal and external customers. | 10/13/2019 |
| 13651 | Cardinal Health Mansfield, MA Engineer, R&D BS/BA Exp: 0-2 years |
Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. Entry level engineer to develop new and improved Surgical Drapes and Gowns, Face Masks, Infection Control Apparel, sterilization wrap. | 10/13/2019 |
| 13652 | Cardinal Health Mansfield, MA Engineer, R&D BS/BA Exp: 0-2 years |
Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. | 10/13/2019 |
| 13653 | Cardinal Health Hazelwood, MO Product Development Engineer I BS/BA in mechanical/biomedical/plastics engineering Exp: 0-2 years |
Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. This position requires an individual to be responsible for supporting the development of new medical devices and improvements to existing products in the medical disposable area. These products are mechanical in nature, and our designs serve a global market. | 10/13/2019 |
| 13654 | Core RX Clearwater, FL Manufacturing Technician HS Diploma/GED Exp: 1-3 years cGMP pharma manufacturing |
Works cross functionally within the organization to facilitate the successful completion of all development projects and meets the objectives and goals of CoreRx Inc. Leads manufacturing projects applicable to the individual’s qualifications. Performs batch instructions to include dispensing of materials, operation of all minor and some major process/blending equipment. Perform physical testing, product inspection, packaging, and general support of the manufacturing operation. | 10/13/2019 |
| 13655 | Cortexyme South San Francisco, CA Clinical Operations Associate BS/BA in biological sciences, health care, or life sciences research Exp: 1-2 years related experience |
The Clinical Trial Assistant provides support to the clinical operations to assist with execution and maintenance of clinical studies. Acts as a central support for the clinical team for designated project communications, correspondence, and associated documentation. Maintains, updates, and may establish various databases for clinical activity tracking. Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites. | 10/13/2019 |
| 13656 | Covance Madison, WI QA Assistant I HS Diploma/GED Exp: Entry Level |
Learn to perform protocol, data and report reviews to verify conformance to applicable SOP and regulatory requirements. Learn to evaluate responses to inspection reports and performs follow-up with respondents, management, or others, if needed, to ensure resolution. Ensures that systems used in QA are properly maintained (e.g., QA audit records, training records). | 10/13/2019 |
| 13657 | Covance Madison, WI Study Technician (Research Assistant) Animal Operations BS/BA in life sciences Exp: 0-2 years |
As a Research Assistant (Study Technician) in our Madison, WI In-Life department, you will monitor the research animals’ health and welfare using your experience in animal observation and your experience working with sample collections. Collection, documentation, and management of pertinent data from animal observations, test material administration, and clinical sample collection. Maintaining the facilities in accordance with the Association for Assessment and Accreditation of Laboratory Animal Care (AALAC) | 10/13/2019 |
| 13658 | Cook Medical Bloomington, IN Regulatory Affairs Specialist I - APAC BS in related field Exp: 0-2 years |
The Regulatory Affairs Specialist I at Cook Inc. is responsible for the planning and preparation of submissions to obtain regulatory approvals for new and modified Class I, II, III and IV medical devices in specific markets. In addition to submissions, the Regulatory Affairs Specialist will serve as a communication liaison between the Cook manufacturer and the Cook Local Office / Cook Distributor. | 10/13/2019 |
| 13659 | Covance Denver, PA mmunology Res Assoc IV BS Exp: 1-2 years |
Working knowledge of ELISA (50% titer), competition assay, neutralization assay and ligand finding assays, and different platforms are essential. This role supports tissue culture and Immunochemistry laboratories. Plans assigned workload on a daily basis and effectively schedules multiple assignments. Learn to identify problems, determine appropriate actions and implement solutions with support as appropriate. | 10/13/2019 |
| 13660 | Cardinal Health Reno , NV Associate II, Warehouse Operations HS Diploma/GED Exp: 1-2 years |
Warehouse Operations is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. Also responsible for the efficient flow of products from the point of product receipt from vendors to the shipment of products (via prescribed service parameters) to a variety of internal and external customers. | 10/13/2019 |
| 13661 | CordenPharma Boulder, CO Chemist BS/BA in chemistry Exp: 0-2 years |
Responsible for ensuring the chemistry of assigned processes is robust and is capable of meeting yield, throughput and QEH&S goals. Identifies process improvement opportunities on existing processes and helps implement solutions. Participates in technology transfers. Troubleshoot assigned processes and identifies and implements problem prevention solutions. Performs and interprets in process control checks. | 10/13/2019 |
| 13662 | CordenPharma Boulder, CO Operations Procedures, Technical Writer BS/BA Exp: 0-5 years in technical writing |
The Operations Procedures, Technical Writer is responsible for optimizing the process to generate Operations Procedures and acts as the primary resource for authorship of procedures used by the Operations department (e.g. master batch records, process manuals, training documentation, operating manuals, etc.). The Technical Writer is responsible for ensuring that these documents are delivered on time, in a compliant fashion and to the standards expected by the team that own, execute and use the documents. | 10/13/2019 |
| 13663 | Cirtec Brooklyn Park, MN Assembler I HS Diploma/GED Exp: 1 year microscope experience |
This position is primarily responsible to perform assembly operations according to written procedures in the clean room environment meeting all quality standards. Be familiar with and follow operating requirements including GMPs (Good Manufacturing Practices) and specific customer defined requirements. | 10/12/2019 |
| 13664 | CliniLabs West Coast, Mid-West, South, Clinical Research Associate (CRA) BS/BA in life sciences, nursing, or related Exp: 1 year or more as clinical monitor |
The Clinical Research Associate (CRA) monitors activities at clinical trials sites to assure adherence to Good Clinical Practices (GCP), standard operating procedures, and study protocols. The CRA reviews regulatory documents as necessary, and prepares site visit reports. The person in this position is involved in the selection of potential clinical investigators and determines if facilities are adequate based on protocol requirements. | 10/12/2019 |
| 13665 | Coating Place Inc. Verona, WI QC Analytical Chemist BS/BA in chemistry or related Exp: 0-2 years |
The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. In addition, support is provided by ensuring the essential job functions of this position are completed as part of the daily and/or weekly schedule.The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. In addition, support is provided by ensuring the essential job functions of this position are completed as part of the daily and/or weekly schedule. | 10/12/2019 |
| 13666 | Codexis Redwood City, CA Research Assistant/Associate (Biochemistry) BS/BA in Biochemistry, Biotechnology, Molecular Biology, Chemistry, or related field Exp: Internship experience preferred but not required |
Assist in developing relevant enzyme assays in HTP format. Execute HTP screens to evaluate enzyme performance under application-relevant conditions. Analyze HTP samples in HPLC, UV-Vis Spectrophotometry, GC, LC-MS, or GC-MS to identify and quantify small-molecule products. Grow cultures, express proteins, and test enzyme activity in high throughput and in larger scales | 10/12/2019 |
| 13667 | Cogent Scientific San Diego, CA Analytical Chemist BS/MS-Chemistry Exp: 1+ years of related experience |
The position will focus on implementing and utilizing state-of-the art automation, analytical and preparative scale chromatographic systems to deliver high quality compounds for drug discovery in the first in-class Automated Life Sciences Studio facility located in La Jolla, CA. Providing new options for the continuous development of processes and chromatographic methodologies that will improve the productivity, timeliness and scientific impact of analytical support. | 10/12/2019 |
| 13668 | Coloplast Minneapolis, MN Consumer Care Advisor BS/BA or AS/AA Exp: 1-6 years in healthcare customer service/sales |
You will be primarily responsible for the support and education of end-users, caregivers, and clinicians with Coloplast products and services. Acquire and demonstrate all necessary subject matter expertise to provide responses regarding product application and problem resolution to clinicians and end-users. Accurately and thoroughly document each end-user program enrollment in Coloplast systems per standard department procedures. Responsible for data quality, including self-audit of work | 10/12/2019 |
| 13669 | Complete Genomics San Jose, CA Research Associate BS or MS in engineering Exp: 1-3 years |
Advanced Engineering group of BGI Research USA is seeking to bring a highly motivated fixed-term Research Associate candidate to provide aid with advanced microfluidic research and development under the direction of a project leader and/or senior engineers and scientists. Maintain and run different aspects of microfluidic systems – reagents, software, hardware. Conduct assays, fluidic and platform validation and verification tests by following defined protocols for microfluidic devices and analyze the data to generate testing reports. | 10/12/2019 |
| 13670 | Complete Genomics San Jose, CA Lab Technician BS/BA in molecular biology Exp: 1-2 years |
his position provides an opportunity to work with cutting-edge technologies and contribute to BGIA’s goal of improving human health by providing genomic information to understand, prevent, diagnose, and treat diseases and conditions. As a member of the BGIA Support team, the position will support next generation processes for genome sequencing. The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing | 10/12/2019 |
| 13671 | Conagen Inc Bedford, MA Scientist/ Research Associate -Protein Biochemistry MS in biochemistry, molecular biology, or related Exp: 1+ years of related experience |
We are currently seeking an associate scientist to support the projects related to metabolic engineering of plant and microbial secondary metabolites. This position will focus on protein engineering and the candidate is expected to have a strong background in protein engineering, biochemistry, molecular biology and be able to translate protein structural concepts into novel protein engineering strategies. | 10/12/2019 |
| 13672 | Conagen Inc Bedford, MA Receptionist/Administrative Assistant HS Diploma/GED Exp: 1 year in office setting |
We are looking for a Receptionist/Administrative Assistant to join our team. This person would assist our Administrative team in overall office and administrative activities as well as be the first point of contact in our offices. Maintains security by following procedures; monitoring logbook; issuing badges. Maintains records by scanning documents, labeling inventory, filing packing slips, updating spreadsheets, processing online scientific journal article requests. | 10/12/2019 |
| 13673 | Conformis Wilmington, MA Production Quality Engineer BS in engineering or sciences Exp: 1-3 years in QA/QE |
The Production Quality Engineer will be responsible for product quality engineering, quality assurance, and production process activities. They will be expected to provide support to Operations, interact with customers and provide support for Design Engineering, Quality Systems and Process Engineering. This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures from concept through market introduction. | 10/12/2019 |
| 13674 | Conformis Wilmington, MA Manufacturing Engineer I BS/BA in engineering, MS preferred Exp: 1-3 years in manufacturing process support/development |
The Manufacturing Engineer I will be responsible for the selection, development, qualification, and scale-up of production processes and equipment across different manufacturing departments. Process objectives are the high quality, high volume production of patient-tailored implants and associated instruments. | 10/12/2019 |
| 13675 | ConMed Utica , NY Quality Engineer I BS in engineering (mechanical/biomedical) Exp: 0-3 years |
We are seeking a self-driven and continuous improvement-focused Quality Engineer I to join our Utica, NY based Quality Engineering team. In this role, you will work cross-functionally to support production lines for a variety of medical devices. You will execute projects aligned with CONMED's Quality System, ISO 13485 standards, risk management, test methods, calibration and product line support. Your efforts in problem solving, innovation and cross-functional collaboration will directly contribute to taking the site's safety, quality, delivery and cost metrics to the next level. | 10/12/2019 |
| 13676 | ConMed Utica , NY Associate Assembler HS Diploma/GED Exp: 3+ months work experience |
As a Team Assembler I, you will perform basic packaging and shipping functions to include basic machine and equipment operation to fabricate parts for assembly and sub-assembly. | 10/12/2019 |
| 13677 | ConMed Utica , NY Packaging Engineer I BS in packaging engineering or related Exp: 0-2 years related |
his engineer will have immediate opportunities to contribute to ongoing sustaining, and new product packaging initiatives working alongside other experienced Packaging Engineers, as well as cross-functionally with manufacturing, project management, R&D, procurement, regulatory, marketing, quality and operations team members. This is an excellent entry level opportunity for an engineering graduate seeking a role with accountability and a path to advance within a growing international medical device company based out of Utica, NY, with multiple manufacturing and design sites across the US. | 10/12/2019 |
| 13678 | Color Burlingame, CA Clinical Lab Assistant BS/BA in sciences preferred Exp: 0-2 years |
As a Clinical Lab Assistant, you will be responsible for assisting in daily clinical operations, primarily involving the performance of a novel clinical test for understanding genetic risk for specific diseases while working in a high complexity CLIA-certified laboratory. | 10/12/2019 |
| 13679 | CliniLabs New York, NY Clinical Research Coordinator BS/BA in sciences preferred Exp: 1-2 years in clinical research |
The Clinical Research Coordinator (CRC) is primarily responsible for coordinating the operational aspects of ongoing clinical projects to ensure that the clients’ goals of time, cost, and quality are met. The CRC may serve as the primary contact with the client to ensure appropriate communications, project budget management, and meeting of timelines. The CRC may also serve as the project lead responsible for directing internal teams in the execution of the protocol and ensuring that all staff working on any given protocol have been properly delegated by the Principal Investigator and adequately trained on the protocol. | 10/12/2019 |
| 13680 | Cogmedix West Boylston, MA Electrical Engineer I BS/BA in electrical engineering Exp: 0-5 years design/development |
As a member of the engineering services team, the Electrical Engineer I will solve complex problems and participate in the specification, design, prototyping and testing of a diverse range of tooling, fixtures, design for manufacturability projects, and other customer product design needs. Under the direction of the Electrical Engineering Manager, the engineer in this role will be performing design tasks of a complex technical nature requiring investigation of new technologies, and applying engineering design principles and practices. | 10/12/2019 |
| 13681 | Cepheid Sunnyvale, CA Associate Scientist MS in biological sciences Exp: 0-2 years |
This position is in the Biotechnology R&D group and is primarily a bench level job focusing on real time PCR assay and product development in an FDA-QSR and ISO13485 compliant organization. The ideal candidate will have experience in general molecular biology methods such as nucleic acid extraction and real-time PCR. This candidate will assist in the development of novel assays for diagnosis and monitoring of microorganisms involved in infectious diseases. In addition to technical qualifications, the ideal candidate will be highly goal-oriented, inquisitive, organized, and be able to thrive in an atmosphere of shifting demands and priorities. | 10/11/2019 |
| 13682 | Phenomenex Torrance, CA Research Scientist MS in chemistry or life sciences Exp: 1-3 years |
Work with R&D team to develop, enhance or investigate new and/or existing separation products and technology. Work with synthetic and analytical chemists in developing new HPLC, SPE and Biotechnology products/methods. Take responsibility for new product development, manufacturing or analytical techniques used to create/improve products and technolo | 10/11/2019 |
| 13683 | Certara Wilmington, DE Quality & Compliance Associate BS/BA Exp: 1-2 years related experience |
The Quality and Compliance Associate is a key member the company’s SOP Committee actively enforcing the company’s policies and procedures in alignment with the overall Quality Management System (QMS). Maintains and promotes company and regulatory quality standards. Conducts activities involving quality assurance and compliance with applicable requirements. Responds to compliance questionnaires | 10/11/2019 |
| 13684 | Ceva Lenexa, KS R&D Technician I BS/BA in microbiology or biology Exp: 1-2 years in lab |
To assist in the development and licensure of viral, bacterial and/or recombinant vaccines as well as new label claims or product improvement research of the licensed vaccines. Propagate cell, virus, bacteria and recombinant organism stocks, perform the testing such as cell counting, titrations, ELISA and other biological and/or molecular assays. Participate in planning and executing from research to large production scale up projects | 10/11/2019 |
| 13685 | Ceva Lenexa, KS R&D Technician I BS/BA in microbiology or biology Exp: 1-2 years in lab |
To assist in the development and licensure of viral, bacterial and/or recombinant vaccines as well as new label claims or product improvement research of the licensed vaccines. Propagate cell, virus, bacteria and recombinant organism stocks, perform the testing such as cell counting, titrations, ELISA and other biological and/or molecular assays. Participate in planning and executing from research to large production scale up projects | 10/11/2019 |
| 13686 | Ceva Lenexa, KS Mareks Lab Technician I BS/BA preferred but not required Exp: lab experience prefered but not required |
Technicians assist in tissue and viral culture of Chicken Embryo Fibroblast (CEF) cells for Marek’s Disease vaccine production in a clean room laboratory environment. Tissue culture is currently performed using roller bottle tissue culture vessels. The production of the vaccine begins in the Marek’s laboratories with the receipt of highly concentrated primary CEF cell suspension; this suspension is then added to a growth medium made in house by technicians. Calculations are performed to reach a target cell amount per roller bottle vessel. | 10/11/2019 |
| 13687 | cGMP Validation Kansas, MO Validation and Compliance Specialist Opening HS Diploma/GED Exp: 1-2 years |
Immediate need for Validation Specialist with experience in the Pharmaceutical and Biotech industry generating and executing protocols for equipment and utilities. Good writing skills a must. Overtime and some travel may be required. Submit resume along with availability | 10/11/2019 |
| 13688 | Champions Oncology Rockville, MD Research Technician I, Necropsy BS in biology, pharmacology, or related Exp: 1 year related experience |
Support in vivo oncology studies in mice as a member of Necropsy Services. Allocate animals to study. Assist with gross necropsies (dissection, tissue trimming/collection/preservation, sample collection). Perform preparation activities, including container and tube labeling and room set-up | 10/11/2019 |
| 13689 | Champions Oncology Rockville, MD Research Technician I, Surgical Services BS in biology, pharmacology, or related Exp: 1 year related experience |
Support in vivo oncology studies in mice as a member of the MDC Team. Receive, characterize and orthotopically or heterotopically surgically implant tissue samples. Conduct tumor volume measurements and sample collection for in vitro characterization. | 10/11/2019 |
| 13690 | Champions Oncology Rockville, MD Laboratory Research Associate BS or MS in biological sciences Exp: 1-2 years lab experience |
Perform laboratory tasks in support of development of immuno-oncology platform. Preparation and handling of primary specimens, including peripheral blood, ascites, other liquid biospecimens. Isolation of white blood cells by density gradient separation. Sample preparation (murine or human tissues/cells) for Flow Cytometry and Immunostaining. | 10/11/2019 |
| 13691 | Champions Oncology Rockville, MD Vivarium Operations Technician I BS in biology, pharmacology, or related Exp: 1 year related experience |
Support in vivo oncology studies in mice as a member of the Vivarium Operations Team. Clean equipment, rooms and facility according to a schedule devised by senior personnel; including floor sweeping and washing, cage washing and sterilization, and waste removal. Provide animal care including feeding and watering with food and water consumption monitoring. | 10/11/2019 |
| 13692 | Champions Oncology Rockville, MD Research Technician I, Study Services BS/MS in biology, pharmacology or related Exp: 1 year related experience |
Support in vivo oncology studies in mice as a member of the Study Services Team. Perform in-life technical procedures, handle, restrain, and provide care for all animals. Provide animal welfare assessments, including body weight and tumor volume measurement. Provide preoperative animal care | 10/11/2019 |
| 13693 | Charles River Boston, MA Surgical Veterinary Technician BS in animal sciences/verterinary technology Exp: 1 year animal handling |
Reviews and complies with all policies pertaining to the animal care program. Cares for and maintains laboratory animals in accordance with USDA Animal Welfare Act and policies, the “Guide for the Care and Use of Laboratory Animals,” and other applicable regulations and policies. Works closely with the Veterinarian to perform daily health assessments of the large animals in the Surgical Services Program and maintain all records as needed and associated with this monitoring. Provides animal treatments as instructed by the Veterinarian. Performs technical functions required by research protocols, such as daily clinical observations, diagnostic testing, administering medications to post-operative animals and health examinations of sick animals, prior to reporting adverse findings to Veterinarian responsible for that area. | 10/11/2019 |
| 13694 | Charles River Horsham, PA Research Technician 1 HS Diploma/GED Exp: 0-6 months animal research experience |
Generate data in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Collect and record research data and biological specimens in compliance with Good Laboratory Practice Regulations (GLPs), study protocols and Standard Operating Procedures (SOPs). Perform basic in-life technical procedures upon completion and sign-off of specific skill training. (e.g., clipping, handling, binding, removals, body weight, dosing). | 10/11/2019 |
| 13695 | Charles River Reno, NV Research Assistant 1 (Formulations) BS/BA in lab sciences Exp: 0-2 years related |
This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 10/11/2019 |
| 13696 | Charles River Norwich, CT Farm Technician HS Diploma/GED Exp: 1 year related experience |
We are seeking a Farm Technician to support our Avian farms located in the greater Norwich, CT area. The Farm Technician will assist where needed in the areas of hatchery, brooding, house management, egg processing, egg pickup, packing, crew and grounds. Assist in a number of different areas on the farms: hatchery, poultry houses (brooding and production), egg processing, packing, egg pickup, house recycles, vaccine bird houses, bird moves, and grounds upkeep. | 10/11/2019 |
| 13697 | Charles River Ashland, OH Research Technician Assistant, Technical Operations HS Diploma/GED, BS preferred Exp: 0-1 year animal research/husbandry |
The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 10/11/2019 |
| 13698 | Charles River Mattawan, MI Quality Control Associate - Cellular Molecular Biology BS/MS Exp: 0 years |
A Quality Control Associate is responsible for verification and archival of study data and departmental records according to established Standard Operating Procedures (SOPs), protocols, methods, and processes. The individual in this role contributes to the team by working independently, completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others. | 10/11/2019 |
| 13699 | Charles River Boston, MA Research Technician I, Technical Operations HS Diploma/GED Exp: 0-1 years in animal research/husbandry |
The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 10/11/2019 |
| 13700 | EyeCRO Oklahoma City, OK Research Assistant-Chemistry(OKC Lab) BS/BA in chemistry, engineering, biotechnology, or pharmacy related Exp: 1 year related experience |
This Person will be responsible for participating in a wide variety of laboratory-based activities related to chemistry to advance our innovative MiDROPS platform as well as animal procedures | 10/11/2019 |
| 13701 | Chemic Laboratories Canton, MA Analytical Chemists BS/BA Exp: All Levels (including Entry) |
Perform routine analytical procedures utilizing a variety of analytical techniques with minimal supervision. Perform method development under the direction of a senior level chemist. Accurately record and document raw data, observations and pharmacy usage. Ensure that work conforms to appropriate regulatory requirements, including SOP’s, Protocols, US FDA and US EPA Good Laboratory Practices (GLP) and US FDA current Good Manufacturing Practices (cGMP). | 10/11/2019 |
| 13702 | Chemic Laboratories Canton, MA QAU Auditors - All levels BS/BA Exp: All Levels (including Entry) |
Review of documentation for conformance to established procedures and regulatory guidelines. Ensure that work conforms to appropriate regulatory requirements, including SOP’s, US FDA and US EPA Good Laboratory Practices (GLP) and US FDA current Good Manufacturing Practices (cGMP). Perform QA functions in support of cGMP manufacturing as necessary. | 10/11/2019 |
| 13703 | Chemic Laboratories Canton, MA Analytical Technical Report Writer - All levels BS/BA Exp: All Levels (including Entry) |
Ability to write technical/scientifically detailed text reports according to established procedures and regulatory guidelines. Auditing and/or experience as an analytical chemist is preferable. Perform reporting functions for GLP/cGMP and R&D data as necessary. Ensure that work conforms to appropriate regulatory requirements, including SOP’s, US FDA and US EPA Good Laboratory Practices (GLP) and US FDA current Good Manufacturing Practices (cGMP). | 10/11/2019 |
| 13704 | ChemPacific Baltimore, MD Chemist MS in chemistry or organic chemistry Exp: 1 year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. | 10/11/2019 |
| 13705 | Celsius Cambridge, MA Animal Care Technician HS Diploma/GED Exp: 1 or more year in animal facility |
The successful candidate will join the Animal Care Team at Celsius Therapeutics in Cambridge, MA to ensure extraordinary animal welfare, compliance, and prime upkeep of the Animal Care Facility. Monitor daily animal health and welfare while performing daily animal health observations. Perform animal husbandry duties to maintain quality and health of research animals, including: performing daily water bottle and cage checks; provide appropriate food, water, and enrichment; perform cage changing as required; record and treat animal health concerns per SOP and/or specified protocols. | 10/11/2019 |
| 13706 | Millipore Sigma Burlington, MA Sales Support Specialist BS/BA in business, chemistry, biology, or related Exp: Recent graduate |
In this role as a Sales Support Specialist you will be required to interact with internal and external customers from quotation generation through the Purchase Order processing phase. You will perform research using a variety of different databases including MilliporeSigma’s customer history database, service management database, contract management database, installation database and financial database. All of which store inquiries and information that MilliporeSigma has received from a customer and/or prospective customer. etc. | 10/8/2019 |
| 13707 | Millipore Sigma Burlington, MA Maintenance Contract Sales Rep. BS/BA in business, chemistry, biology, or related Exp: Recent graduate |
The role of Maintenance Contract Sales Representative will require the candidate to interact with internal and external customers from quotation generation through the Purchase Order processing phase. They will generate quotes for new and renewal of service agreements for current MilliporeSigma customers. Should be able to work independently to manage new and renewal service agreements within a defined geographical territory. etc. | 10/8/2019 |
| 13708 | Millipore Sigma St. Louis, MO QC Logistics Technician AS in life or physical sciences Exp: Recent graduate |
You will assist in evaluating safety practices with regard to team activities. Work both independently and in team environment. Manage sample inventory and department stock room. Troubleshoot interruptions to the normal process flow. Manage Quality and Retain Samples. Use lean and six sigma practices to optimize efficiency and eliminate waste from process. Adhere to process requirements in a continuously changing environment. etc. | 10/8/2019 |
| 13709 | Millipore Sigma St. Louis, MO Associate Production Scientist BS/BA in chemistry or other science Exp: 1+ years |
Manufacture products according to established protocols and perform operations to support a chemical manufacturing department located in St Louis, MO. Physical Attributes: Will be frequently required to wear appropriate personal protection equipment “PPE” (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes, etc.) for protection from toxic or corrosive chemicals in the forms of liquids, solids, and/or vapors. While performing the duties of this job, the employee is regularly required to sit, stand, walk, reach above the shoulder, stoop, kneel, or crouch. etc. | 10/8/2019 |
| 13710 | Millipore Sigma St. Louis, MO Customer Care Associate High school diploma/AS Exp: 1+ years |
The Customer Care Associate position involves working in a dynamic, fast paced, high energy call center, and rewarding team environment focused on delivering a better customer experience. You will be responsible for ensuring each transaction is processed within customer specifications for MilliporeSigma guidelines. As a Customer Care Associate, you must be eager to learn, be respectful, honest & humble, and embrace challenges. etc. | 10/8/2019 |
| 13711 | Millipore Sigma Burlington, MA Service Support Specialist High school diploma or equivalent Exp: 1+ years |
In this role you will establish and maintain service schedules with customers, prepare and process repair quotations and manage service inventory. In addition, you will support installation orders by insuring sites are prepared for service and support the service partners. You will create an efficient service schedule to maximize resources, ensure material is on site and accurate. Coordinate service-related activities as guided by service engineers and managers. etc. | 10/8/2019 |
| 13712 | Miltenyl Biotec Auburn, CA Accounting Associate AS/BS/BA Exp: 1-3 years |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. etc. | 10/8/2019 |
| 13713 | Miltenyl Biotec Santa Barbara, CA Assembly & Test Technician AS/AA Exp: 1-3 years |
To support this effort, we are seeking an Assembly and Test Technician to support the assembly of designed parts for the company’s core medical instruments. Within this role, you will be responsible for supporting all tasks and functions in producing interposer to chip assemblies, while inspecting incoming raw materials and maintaining inventory for all production parts. Overall, your keen ability to work with a multi-disciplinary team to lead and advance product development efforts will champion the continued success of Owl biomedical. etc. | 10/8/2019 |
| 13714 | Miltenyl Biotec Sunnyvale, CA Manufacturing Associate BS in a biological science or related Exp: 1-3 years |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. etc. | 10/8/2019 |
| 13715 | Miltenyl Biotec Sunnyvale, CA Process Development Associate BS in a life science Exp: 0-2 years |
As a member of Miltenyi Biotec’s Process Development team, you will have the exciting opportunity to support the development of new processes that will generate cellular therapeutic products. You will apply your GLP/GMP experience to perform and maintain cell cultures using aseptic techniques. Ideally, you will be able to order materials and maintain inventory with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical cell and gene therapy products. etc. | 10/8/2019 |
| 13716 | Miltenyl Biotec Gaithersburg, MD R&D Scientist, Purification & Characterization MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to develop methods for the separation of different particle types and their characterization. Also, you will develop, evaluate and implement novel analytical methods for the fine characterization of viral vectors and exosomes, in view of the distinction of viral vectors from exosomes. You will design specific experiments to test LV function, perform statistical analysis of results, and communicate results internally, for use in publications, and in scientific meetings. etc. | 10/8/2019 |
| 13717 | Miltenyl Biotec Gaithersburg, MD Research and Development Scientist, RCL/HIV MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to perform duties within the area of development of new tests, including the development of a standard RCL test and in a second instance of an automatized RCL test. This includes the set-up of a standard test based on the use of C8166 cells, the characterization of the C8166 cells with respect to susceptibility and propagation of HIV over many cell passages, etc. A very issue related to this development is that the test has to comply with FDA requirements with at the end the transfer of the test to the QC department for routine use. etc. | 10/8/2019 |
| 13718 | Mizuho San Diego, CA Field Service Engineer AS in electrical or mechanical applied science Exp: 1-2 years |
The Field Service Engineer (FSE) is primarily responsible for technical support, repairing and servicing Mizuho OSI products (orthopedic equipment) in the field throughout the United States. The Field Service Engineer provides highly visible customer support through the performance of on-site installation, as well as overseeing any necessary diagnoses, troubleshooting, service, and repair of complex equipment and systems, and performing preventive maintenance as required. etc. | 10/8/2019 |
| 13719 | Moderna Cambridge, MA Senior Research Associate, Drug Product Process Sciences MS in pharmaceutical science or related Exp: 1 month relevant work |
Reporting to the Principal Scientist, Process Development, the Senior Research Associate, Drug Product Process Sciences will work with in vitro bioanalytical systems to evaluate samples from in vivo studies. The successful candidate will be able to deliver reproducible and impactful results under ambitious timelines. Here’s What You’ll Do: Develop and characterize lipid nanoparticle (LNP) formulations for delivery of mRNA. etc. | 10/8/2019 |
| 13720 | MP Biomedicals Irvine, CA Fine Chemicals Specialist BS/MS in chemistry, biology or related Exp: 0-3 years |
The Fine Chemicals Specialist is responsible for developing and maintaining technical documentation for industrial and pharma customers. This role works closely with our global Fine Chemicals sales team to provide rapid response to customer requests for quote of new or existing products. Principal Duties & Responsibilities: Build required product documentation. Adjust documentation per customer requirements. Manage supplier qualification in alignment with MP Bio’s ISO procedures. etc. | 10/8/2019 |
| 13721 | Myriad Austin, TX Research Associate MS Exp: 1+ years |
Myriad RBM is hiring a Research Associate Development who will plan, perform, evaluate, and propose experiments within a project(s) to provide valid and needed information. You will also plan, design, development, optimization, validation, qualification, and implementation of immunoassays. Responsibilities: Conduct assigned experiments and assists in their designs. Follow directions and laboratory procedures as assigned by supervisor. Perform Luminex and ELISA assay development, optimization, validation and execution. etc. | 10/8/2019 |
| 13722 | MTEM Austin, TX Manufacturing Associate - Downstream BS in life science or related Exp: 1 year |
Molecular Templates is seeking an experienced and highly-motivated professional to support downstream processing for manufacturing activities. This position will perform functions related to production and manufacturing operations, including routine protein purification, equipment maintenance checks and calibration, data management, and assist in review and development methods and procedures to control or modify the manufacturing process. This position will also aid in identifying continuous process improvement areas. etc. | 10/8/2019 |
| 13723 | MTEM Austin, TX Research Associate, Cell Biology BS in life science or related Exp: 1+ years |
Molecular Templates is seeking a highly-motivated and skilled Research Associate to support research and development activities. This position will be primarily responsible for maintaining cell lines, conducting cellular cytotoxicity assays and performing flow cytometry in accordance to established protocols, and performing general laboratory duties, including washing glassware, ordering supplies, and maintaining inventory and basic laboratory equipment. etc. | 10/8/2019 |
| 13724 | MTEM Austin, TX Manufacturing Associate - Upstream Development BS in life science or related Exp: 1+ years |
Molecular Templates is seeking an experienced and highly-motivated professional to support upstream processing for manufacturing activities. This position will perform functions related to production and manufacturing operations, including routine microbial fermentation, equipment set-up and calibration tasks, media preparation, quality testing, process documentation, and assist in review and development methods and procedures to control or modify the manufacturing process. etc. | 10/8/2019 |
| 13725 | Millipore Sigma Madison, WI Scientist, Quality Associate BS in chemistry or related biological science Exp: 0-2 years |
The Scientist, Quality Associate position is responsible for the routine analysis of samples in the Quality Control department and all related cGMP paperwork. Analysis involves the use of HPLC, GC, KF, DSC, TGA, Titration, and IR among other tests and instruments. This position is also responsible for assisting with method qualification/validation, writing protocols and standard operating procedures. etc. | 10/8/2019 |
| 13726 | CaREdX Brisbane, CA Clinical Laboratory Assistant AA, BS/BA in biological sciences Exp: 1-3 years |
The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed. | 10/6/2019 |
| 13727 | CaREdX Brisbane, CA Clinical Laboratory Assistant AA, BS/BA in biological sciences Exp: 1-3 years |
The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed. | 10/6/2019 |
| 13728 | Caribou Biosciences South San Francisco, CA In vivo Pharmacology Research Associate BS/BA in life sciences Exp: 1 or more year lab work w/rodents |
The candidate must be motivated, enthusiastic, professional and committed to working as a team player. The ideal candidate enlists confidence, comfort and a working knowledge of laboratory animals, with a background in animal husbandry, restraint and handling. In addition, experience with injection (IV, IP, SC, and PO) and blood draw techniques (RO bleed and cardiac puncture), along with rodent surgery and anesthesia experience is desirable. The candidate must have the ability to effectively communicate with coworkers, take direction from supervisors, and be accountable for their actions. | 10/6/2019 |
| 13729 | Caris Life Sciences Phoenix, AZ Customer Support Representative- Oncology AS/AA in relevant field Exp: 1-3 years in client service roles |
A Customer Support Representative acts on behalf of Caris as the first tier of support for all client issues or needs. This position responds to internal and external client inquiries regarding logistics, testing, supplies, and other support needs. This position handles all incoming documentation into the department. Independent judgment is required to carry out assignments that have a significant impact on clients. | 10/6/2019 |
| 13730 | Casma Therapeutics Cambridge, MA Research Associate--Cell Lines, Biology MS in biological sciences Exp: 1-3 years |
The individual should possess strong core competencies in cell biology, molecular biology, assay development. We are seeking a qualified candidate who will share our excitement about the science, contribute to our culture, and honor our commitment to patients. Perform western blotting, FACS and imaging analysis to analyze autophagy and specific target activity in primary cells and cell lines. Cell culture and cell line development using retro- and lenti-virus, CRISPR and downstream analysis of autophagy and signaling. | 10/6/2019 |
| 13731 | Catalent Madison, WI Associate Scientist, Quality Control Microbiology BS/BA in biotechnology Exp: 0-2 years |
The Associate Scientist, Quality Control Microbiology position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate can be trained on technical procedures and once trained, execute them consistently and reliably. Additionally, this position will support Preventative Maintenance and basic Laboratory maintenance activities while maintaining a GMP quality system. The Associate will work on assignments that are primarily routine in nature but also provides support on projects and conducts lab work involving additional complexity. | 10/6/2019 |
| 13732 | Catalent Madison, WI Assistant Scientist, Upstream Process Development MS or BS/BA in biolotechnology Exp: 1-3 years lab experience |
The Assistant Scientist, Upstream Process Development will perform a variety of laboratory procedures to support Upstream Process Development. The position will perform daily work assignments accurately and in a timely and safe manner. This position will independently evaluate, select and apply standardized scientific and techniques; assignments have clear and specified objectives, and require the investigation of a limited number of variables. This position relies on limited experience and exercises judgment within defined procedures and practices in making minor adaptations and modifications. | 10/6/2019 |
| 13733 | Catalent Madison, WI Associate, Biomanufacturing Operations BS/BA in biotechnology Exp: 0-2 years |
Catalent has an entry level Associate, Biomanufacturing position available. As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position offering enticing compensation incentives. Work hours are Wednesday to Saturday (4/10). | 10/6/2019 |
| 13734 | Catalent Madison, WI Associate, Biomanufacturing BS/BA in biotechnology Exp: 0-2 years |
Catalent has an entry level Associate, Biomanufacturing position available. As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position. Work hours are Sunday to Wednesday (4/10). | 10/6/2019 |
| 13735 | Catalent Madison, WI Manufacturing Associate, Drug Substance Downstream AS/AA or BS/BA Exp: 0-2 years GMP experience |
A manufacturing associate’s primary duty is to perform a variety of operational tasks in accordance with current GMP's. Operators must work effectively in a team environment to achieve company goals and must adhere to all company compliance, safety, and attendance requirements. Safely operates equipment within a preparation area (i.e. cleaning, steamings, buffer/media prep, parts washing, autoclaving, etc) | 10/6/2019 |
| 13736 | Catalent San Diego , CA Analytical Chemist I BS/BA in sciences Exp: 0-2 years |
This a great entry-level opportunity for a new grad looking to gain hands-on industry experience and learn a variety of lab techniques. The Analytical Chemist I will be expected to understand and execute basic analytical procedures in order to assess the quality of pharmaceutical API, intermediates, and final drug products under limited supervision. Duties may include the preparation of simple aqueous and organic buffered solutions, volumetric dilution of samples and standards using good laboratory techniques, clear and accurate record keeping in laboratory notebooks, use of analytical instrumentation to acquire raw data, calculation and reporting of final results. The Chemist I will begin to develop product-specific cleaning methods to support use of GMP manufacturing equipment. | 10/6/2019 |
| 13737 | Catalent Madison, WI Gold Associate: Biologics Track BS/BA Exp: Graduating in 2019-2020 |
The Catalent GOLD Program is a two-year rotational development opportunity designed for university graduates who are excited to accelerate their careers in an entrepreneurial, fast-paced and inclusive environment. If you are ready to meet new challenges head on with creative solutions and unrelenting passion to deliver on the needs of patients around the world, join us. | 10/6/2019 |
| 13738 | Celerion Lincoln, NE Laboratory Equipment Maintenance Technician AS/AA in sciences Exp: 1+ years lab experience |
As the Laboratory Equipment Maintenance Technician, you will be responsible for assisting in the maintenance of bioanalytical equipment. This position offers a chance to work on a wide variety of laboratory equipment that is vital to the clinical research process. Assists with the setup, operation, evaluation and troubleshooting all types of bioanalytical laboratory instruments, including interfacing with LCMSMS, pumps, water baths, plate washers, plate readers, incubators, etc. | 10/6/2019 |
| 13739 | Cell Signaling Technologies Danvers, MA Product Marketing Coordinator BS in lifes ciences with business concentration or related Exp: Entry Level |
We are seeking a highly organized Product Marketing Coordinator who will be responsible for supporting product marketing lifecycle management related projects, including product line discontinuations, product conversion campaigns, market research and promotions. This is an exciting opportunity for someone with strong analytical skills looking to work in a fast-paced, collaborative team setting where they can experience multiple facets of Product Marketing. | 10/6/2019 |
| 13740 | FuijiFilm Madison, WI Laboratory Technician BS/BA in biological sciences/chemistry or related Exp: 0-2 years |
FUJIFILM Cellular Dynamics, Inc in Madison, WI is recruiting for a laboratory technician. This role provides an outstanding opportunity for talented and self-motivated individuals working with our R&D teams. Ideal candidates will have exposure to cell culturing and will be interested in advancing their career to support our ongoing efforts to generate differentiated cell types from human induced pluripotent stem cells. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and life science products and tools to support research endeavors. In return we provide development and support to enhance your career development in the field of cutting edge iPSC technology. | 10/6/2019 |
| 13741 | Cell Signaling Technologies Danvers, MA Research Associate - Chromatin IP (ChIP) BS/BA or MS in biological sciences Exp: 1+ years lab experience |
We are currently seeking a highly motivated Research Associate to join a team dedicated to the development of epigenetics-based assays. The candidate will contribute to the development of innovative research tools, with a primary focus on antibody validation and assay development for chromatin IP (ChIP), ChIP-Seq and related technologies. Major lab techniques include chromatin preparation, ChIP, DNA purification, PCR, DNA sequencing library preparation and cell culture. Applicants must be able to design moderately complex experiments with proper controls and are expected to independently interpret and report results. | 10/6/2019 |
| 13742 | Bristol-Myers Squibb Syracuse, NY ASSOCIATE ENGINEER I MS in engineering Exp: 0-2 years |
The Manufacturing Technology Associate Engineer will support Manufacturing Operations (Downstream processing, column packing) on a daily basis, as well as lead or contribute to strategic projects. Support projects and identify opportunities for productivity, robustness, quality, business process, and safety improvements. Regular and frequent on-floor observation to support and improve manufacturing. | 10/5/2019 |
| 13743 | Bristol-Myers Squibb Redwood City, CA Associate Research Scientist MS with background in immune-oncology Exp: 0-2 years |
This position will specifically support acquisition, processing, and analysis of human tumor tissue. The candidate will contribute to tumor tissue analysis, including drug response, phenotypic, histoloical, and genomic/transcriptomic analyses of these tissues. The candidate will be expected to effectively collaborate with colleagues in the oncology, translational medicine, biomarker and clinical groups. The successful candidate will demonstrate clear verbal and written communication skills. | 10/5/2019 |
| 13744 | Essity Menasha, WI Entry Level Paper Mill Support HS Diploma/GED Exp: Entry Level |
Support Multi-Million Dollar Fiber Processing and De-inking Assets, working in a Team environment, handling raw materials and finished Tissue parent rolls as necessary. | 10/5/2019 |
| 13745 | BD Salt Lake City, UT Engineer I, R&D Product Development BS in mechanical/biomedical engineering Exp: 0-2 years |
This position designs, develops, and implements new products, processes, test methods and equipment. Initiates new or revised documentation and tracks through appropriate approval cycles and implementation. Maintains a professional working relationship with internal and external customer and support staff. Participates and/or leads cross-functional teams. | 10/5/2019 |
| 13746 | BD Salt Lake City, UT R&D Technician II AA/AS in sciences, math, engineering Exp: 0-5 years |
This position reports to an engineer on the Dialysis Team. An R&D technician helps with the generation of test protocols and reports, tests products and reports results, and helps to design and maintain test fixturing. In addition, they may help with troubleshooting and test development. Assists in the execution of test protocols, methods and procedures. Sets up and operates test equipment and records measurements with limited supervision | 10/5/2019 |
| 13747 | BD Salt Lake City, UT Scientist I BS/BA or MS in molecular biology Exp: 1 year or more |
Scientist I is required to work within a team that develops automated assays using nucleic acid isolation and real-time amplification/detection technologies. Reporting to the Group Leader/Manager, the successful candidate will be responsible for assisting in the design, development, integration and/or qualification of assays on automated systems. The successful candidate may also be expected to provide support in execution of clinical studies to validate performance of the assays and assemble relevant information in support of regulatory submissions. | 10/5/2019 |
| 13748 | BD Franklin Lakes, NJ R&D Engineer I BS in mechanical/biomedical engineering Exp: 0-2 years |
The incumbent will join the Verification & Validation team as an Engineer I, providing support to a cross-functional team. The successful candidate will be responsible for supporting product verification activities and will support test method development activities, measurement system development & analyses, test fixture design. He/she will support the development of design verification strategies and DV execution required for sustaining existing and commercialization of various types of new medical device products used in drug delivery. | 10/5/2019 |
| 13749 | BD Glens Falls, NY Manufacturing Team Member I Bipolar HS Diploma/GED Exp: Prior experiernce preferred but not required |
Performs any combination of tasks involved in the manufacture and assembly of medical devices. Perform a variety of duties to assemble all types and sizes of product, components, and sub-assemblies using a variety of standard and specialty assembly machines or hand operations. May be required to press, bond, solder, flare, strip, clamp, sand, weld, mount/takedown or inspect for appearance, gauging of parts by “no-go” or “go” gauges and set fixtures. | 10/5/2019 |
| 13750 | BD Glens Falls, NY Manufacturing Team Member I HS Diploma/GED Exp: Prior experiernce preferred but not required |
Performs any combination of tasks involved in the manufacture and assembly of medical devices. Perform a variety of duties to assemble all types and sizes of product, components, and sub-assemblies using a variety of standard and specialty assembly machines or hand operations. May be required to press, bond, solder, flare, strip, clamp, sand, weld, mount/takedown or inspect for appearance, gauging of parts by “no-go” or “go” gauges and set fixtures. After initial training, shows the ability to consistently meet daily production goals while building a high quality product, part or subassembly to specification. | 10/5/2019 |
| 13751 | BD Sandy, UT Process Specialist HS Diploma/GED Exp: 1-2 years in manufacturing |
The Process Specialist Operates high speed automated manufacturing equipment in the Surgical Scrub department. Operates high speed automated manufacturing equipment. Ensures that correct doses of the active ingredients are dispersed. Responsible for readying production equipment and materials during product changeovers. Responsible for set-up of work stations and bringing in materials for production order. | 10/5/2019 |
| 13752 | Boehringer Athens, GA Technician I, Packaging Second Shift (2:00pm-9:30pm, Monday-Friday) HS Diploma/GED Exp: 1 year manufacturing experience |
To perform the duties associated with labeling, inspecting and packaging of Boehringer Ingelheim vaccines. Performs and executes with others, all daily scheduled activities associated with packaging vaccines. Label and inspect products accurately and efficiently, to meet quality guidelines. Complete documentation in an accurate, concurrent and timely manner | 10/4/2019 |
| 13753 | Boehringer Fremont, CA Engineer I, MSAT Upstream MS in engineering Exp: 0 years |
The primary purpose of the position is to execute projects, perform routine experiments and analyze data in the Upstream Manufacturing Science and Technology (MSAT) group. The position holder must live the BI values and promote a positive work environment for others. Has discretion in tactical execution of process improvement projects, investigations and experiments. Frequently executes routine and occasionally complex experiments with sound scientific and engineering principals to resolve problems with minimal oversight. The Engineer frequently executes against specific deliverables developed by the department leadership to improve operational efficiency. | 10/4/2019 |
| 13754 | Boston Analytical Salem, NH Microbiologist BS/BA in microbiology or realted Exp: 0-2 years cGMP work environment |
The QC Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity). | 10/4/2019 |
| 13755 | Boston Analytical Salem, NH Lab Technician – Microbiology HS Diploma/GED Exp: no minimal experience required |
The Lab Technician in the Microbiology Lab will perform routine laboratory tasks and assist laboratory personnel according to FDA, cGMP and Boston Analytical’s Standard Operating Procedures. Cleans and maintains laboratory glassware (including sterilization), equipment, and laboratory. Monitors and maintains water system, including sample collection for Bioburden, TOC, and Conductivity. Properly handles, stores and disposes of hazardous materials according to OSHA and Boston Analytical procedures. | 10/4/2019 |
| 13756 | Boston Analytical Salem, NH Lab Technician – Chemistry HS Diploma/GED Exp: no minimal experience required |
The Lab Technician will perform routine laboratory tasks and assist laboratory personnel according to FDA, cGMP and Boston Analytical’s Standard Operating Procedures. Cleans and maintains laboratory glassware, equipment, supplies and laboratory. Properly handles, stores and disposes of hazardous materials. Assists Chemists and other company personnel on an as needed basis. | 10/4/2019 |
| 13757 | Boston Analytical Salem, NH Analytical Chemist *All-Levels* BS/BA in chemistry or related Exp: 0-5 years |
he Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 10/4/2019 |
| 13758 | Boston Analytical Salem, NH QA Specialist – All Levels BS/BA in related sciences Exp: 0-3 years QA experience |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing chemists analytical data, routine work, protocols and reports. Auditing chemists’ routine project folders for conformance to company and customer requirements. Write, review and edit Standard Operating Procedures (SOP’s, Forms and Methods) and familiarity with internal SOPs. Alternate contact person for QA questions relating to laboratory operations and client correspondences. | 10/4/2019 |
| 13759 | Boston Scientific Arden Hills, MN Quality Technician II Job AA degree or higher Exp: 1-2 years in medical device quality |
Provide Quality Technician support to Arden Hills commercial and development manufacturing lines ensuring delivery of the highest quality product to the customer while supporting continuous improvement projects and quality initiatives. This is a dynamic support role requiring cross-functional collaboration with production, manufacturing, and quality team members. This role includes responsibility for providing day-to-day quality support for manufacturing, including the processing of non-conforming product (identification, documentation, segregation evaluation and disposition), certifying builders and responding to quality signals. | 10/4/2019 |
| 13760 | Boston Scientific Maple Grove, MN Quality Engineer I - Design Assurance BS in engineering or related Exp: 0-2 years in engineering |
The Design Assurance Engineer I is a quality engineer that directly supports medical device product development from concept through commercialization. This position will work with high-performance cross-functional development team to establish and maintain the design control deliverables, risk management activities, and DHF compliance within Interventional Cardiology to ensure delivery of the highest quality product to the customer. | 10/4/2019 |
| 13761 | Boston Scientific Arden Hills, MN Product Performance Engineer I BS Exp: 0-3 years |
This Quality Engineer role will investigate product complaints and monitor BSC product performance. The team uses product performance data to escalate post-market field performance signals into the CAPA process in collaboration with Return Device Analysis, R & D, Design Assurance, Medical Safety and the CAPA Management teams. This role provides for significant visibility across the quality organization | 10/4/2019 |
| 13762 | Boston Scientific Maple Grove, MN Technical Writer I BS/BA in technical writing or related Exp: 6 months + related |
This Technical Writer will work as a team member on product development or other technology projects to bring clarity and consistency to documents through accurate and concise writing and effective use of document format. In summary, this tech writer will write, revise, organize, plan, summarize, edit, and proofread technical engineering documents and maintain project records. | 10/4/2019 |
| 13763 | Brammer Bio Somerville, MA Planner I BS/BA Exp: 1-3 years of planning/manufacturing |
Daily planning operations supporting the manufacturing facility; planning for and ensuring availability of raw materials, components, and resources per the site’s detailed manufacturing schedule. Facilitate and coordinate activities with all departments to ensure the availability of raw materials for plant operations supporting development through commercial production. Review cGMP production records and perform associated inventory transactions in the ERP system. | 10/4/2019 |
| 13764 | Brammer Bio Cambridge, MA Engineer I, Process Engineering BS in automation/electrical/chemical/mechanical engineering Exp: 0-3 years |
Responsible for the support of clinical and commercial drug manufacturing in the new Viral Vector Manufacturing facility located at the Cambridge, MA campus. Scope includes designing, specifying, and supporting manufacturing equipment such as autoclaves, incubators and analytical equipment in our newly built viral vector manufacturing facility. Individual will be part of an experienced team of process and automation engineers working closely with groups such as manufacturing, quality assurance, quality control and validation. | 10/4/2019 |
| 13765 | Brammer Bio Cambridge, MA Engineer I, Automation BS in automation/electrical/chemical/mechanical engineering Exp: 0-3 years |
Responsible for the support of clinical and commercial drug manufacturing in the new Viral Vector Manufacturing facility located at the Cambridge, MA campus. Scope includes designing, specifying, and supporting manufacturing systems such as DeltaV, Allen Bradley PLC and analytical equipment in our newly built viral vector manufacturing facility. Individual will be part of an experienced team of process and automation engineers working closely with groups such as manufacturing, quality assurance, quality control and validation. | 10/4/2019 |
| 13766 | Brammer Bio Cambridge, MA Associate I, Process Sciences BS in biochemical/chemical engineering or related Exp: 0-2 years |
he Process Sciences (PS) Associate’s primary responsibility is to support the process establishment, pilot, and process characterization for the manufacturing of viral vectors. This position requires close interaction with the PS colleagues, Manufacturing Science & Technology, Manufacturing, Process Development, and other departments. This role will focus on defining and characterizing robust, scalable and efficient manufacturing processes to produce late-phase human clinical trial and commercial viral vector therapeutics. | 10/4/2019 |
| 13767 | Brammer Bio Lexington, MA Associate I, MFG Nights BS in life sciences Exp: 0-3 years |
Responsibilities include performing basic to moderately complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls. Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities. Must be technically capable with a basic theoretical comprehension of general biopharmaceutical manufacturing equipment, principles and processes and have a basic understanding of current GMP and safety standards. | 10/4/2019 |
| 13768 | Brammer Bio Lexington, MA Associate I, Manufacturing Downstream BS Exp: 1-3 years |
Responsible for cGMP manufacturing operations at the Brammer Lexington site Downstream Operations. Executing aseptic operations within Biosafety cabinet and cleanroom environment. Preparation of buffers to support downstream purification activities. Performing Chromatography, TFF, Viral Filtration, and Final Formulation steps. Performing various filter integrity tests throughout the process. Follows verbal and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation. | 10/4/2019 |
| 13769 | Brammer Bio Cambridge, MA Associate I, Manufacturing BS in life sciences Exp: 1-3 years |
Associate I, Manufacturing is an associate with a moderate level of technical expertise and experience. Associate I may perform complex activities outside of routine manufacturing operations commensurate with their experience and training. Associate I participates in the day to day operation of a cGMP compliant Manufacturing facility. Responsibilities include performing basic to complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls under limited supervision. Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities. | 10/4/2019 |
| 13770 | Bristol-Myers Squibb Hopewell, NJ Associate Biological Technician BS/BA with ALAT certification within 12 months of hire Exp: 0-2 years |
The Associate Biological Technician performs semi-routine or diversified work that requires the ability to differentiate established principles and practices from unique occurrences which may necessitate adapting or modifying methods. May be required to breed and develop animal colonies, collect tissue samples and collect data for routine operations. Perform support duties that involve animal health maintenance, i.e. sentinel program, water and feed evaluation, sanitation sampling and testing, and other related tests, as required | 10/4/2019 |
| 13771 | Bio-techne Minneapolis, MN Lab Assistant 1 AA degree Exp: 0-2 years |
This is a Part-Time position. Your responsibilities as a Laboratory Assistant 1 are to maintain the animal facility at Bio-Techne and perform general lab duties. Responsible for the welfare and immunization of all rodents that are used within R & D Systems. Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job. General lab duties including stocking and organizing supplies and materials and preparing reagents. | 10/3/2019 |
| 13772 | Bio-techne Minneapolis, MN Inside Sales Representative - Bioprocess Service Contracts BS in sciences Exp: 1 year in telemarketing/telesales |
The Inside Sales Representative is primarily responsible for achieving sales quota for ProteinSimple products, initially, Bioprocess (Maurice/iCE/MFI) system service contracts. This person will be located at the Bio-Techne headquarters in Minneapolis, MN, interfacing primarily via the telephone and email with customers and potential end-users in the assigned territory. The secondary role is to gain proficiency on all ProteinSimple products to provide back-up support for field sales reps, and ultimately take on a full-time field sales position. | 10/3/2019 |
| 13773 | Bio-techne Minneapolis, MN QC Specialist 1 BS in biological sciences/chemistry Exp: 1-2 years in vitro diagnostics |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. Assist in establishing QC specifications. Performs analysis and interpretation of test results, identifies deviations, and makes appropriate recommendations | 10/3/2019 |
| 13774 | Bio-techne San Jose, CA Production Chemist I AA or BS/BA in sciences/engineering Exp: 0-3 years in wet-lab manufacturing support |
The successful applicant will work with other members of the consumable production team as well as a multidisciplinary team of engineers and scientists to support routine production activities for reagent formulation/ compounding team. Principal duties and responsibilities: Help maintain and track supplies inventory. Preparation of buffers and other biochemical formulations. Conjugation of protein solutions. Record manufacturing tasks in batch records/travelers. | 10/3/2019 |
| 13775 | Bio-techne San Marcos, CA Packaging Technician HS Diploma/GED Exp: 1-2 years in vitro diagnostics |
Perform kitting, liquid / powder filling and labeling functions. Assist in the setup and running of automated liquid filling, labeling and packaging equipment. Assist in the setup and running of manual liquid and powder portable filling equipment. Comply with Good Manufacturing Practices (GMP’s) and Quality Systems Regulations (QSR). Inspect all materials being issued to and returning from shop orders. Accurately count and return all materials. | 10/3/2019 |
| 13776 | Bio-techne Minneapolis, MN Research Associate, Antibody Purification BS/BA in biological sciences/chemistry or related Exp: 0-2 years |
As an Antibody Purification Research Associate you will be responsible for performing antibody purifications and conducting in process testing of product. Purify monoclonal and polyclonal antibodies following appropriate SOP’s. Prepare buffers as needed for the purification process. Document the purification processes in the appropriate computer systems. Perform routine HPLC and other equipment maintenance. | 10/3/2019 |
| 13777 | Bio-techne Minneapolis, MN Equipment Technician 1 HS Diploma/GED Exp: 1-2 years in equipment maintenance |
As a Equipment Technician 1 you will perform preventative maintenance and repair malfunctioning new and existing minor equipment. Respond and log supervisory alarms on TAC Monitoring System during business hours. Act as the secondary facility maintenance mechanic responsible 24/7 on call for TAC & Security System with department personnel. Assist with installing new and existing equipment, offices furniture and shelves. Perform additional duties as assigned. | 10/3/2019 |
| 13778 | Bio-Technical Resources Manitowoc , WI ASSISTANT RESEARCH SCIENTIST, ANALYTICAL SUPPORT BS/BA or MS in analytical chemistry, chemical engineering or related Exp: 1-3 years |
The position involvesimplementation of HPLC, chromatography, enzyme assays, and gel-basedanalytical methods.Common tasks include analytical separations and quantitative analyses by:1) HPLC and column chromatographyincluding affinity chromatography, IEX, HIC, and SEC; 2) spectrophotometric enzyme assays; 3) sample preparation and extraction;and 4) basic antibody and protein analyses,usingELISA, protein extraction, protein concentration assays, SDS-PAGE, and Western blot. | 10/3/2019 |
| 13779 | BiOTek Winooski, VT Electro-Mechanical Assemblers AS/AA in relevant field Exp: 0-2 years |
Responsibilities include performing assembly and inspection processes, collecting report data as required by Quality standards, maintaining shop supplies, floor stock and tools and knowledge and support for Lean Manufacturing principles. Ability to lift and move units up to 35/40 lbs in weight to 5-foot high levels is required. You may perform product tests and material transaction; learn and support new products and train new employees consistently striving for efficient and effective methodologies. | 10/3/2019 |
| 13780 | Biotium Fremont, CA Research Technician/Research Associate, Bioscience BS/BA or MS in biology or biochemistry Exp: 1 year research experience |
Under the supervision of Biotium scientists, perform production and quality control testing of assay kit components following standardized protocols. Under the supervision of scientists, perform R&D assays to develop new fluorescence-based products. This individual will be responsible for production and QC of products, as well as play a role in the design,optimization and assessment of novel reagents for fluorescent detection technologies. | 10/3/2019 |
| 13781 | Bioventus Boise, ID Associate Sales Representative BS/BA Exp: 0-2 years |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Develop and execute regional business plans to achieve quotas for assigned products, which may include cold calling to develop new customers, qualifying and following up on leads and selling to new and/or existing accounts | 10/3/2019 |
| 13782 | Biovision Milpitas, CA Sales Representative BS/MS in biochemistry, or biological sciences Exp: 1-2 years in life science industry |
Meet or exceed sales objectives set by the BioVision management. Learn and master BioVision's product offering and manufacturing capabilities. Establish long-term relationships with the customers and match BioVision's capabilities with customer needs. Identify key contacts and decision makers to maximize the benefits from customer visits. Develop a customer-specific account management approach, identifying new business and growth opportunities | 10/3/2019 |
| 13783 | bluebird bio Cambridge, MA Cellular Process Development & Gene Editing Specialist BS in biological sciences Exp: 0-2 years |
The cellular process development teams are responsible for developing cellular drug product processes and introducing new technologies for stem cell and T-cell therapies. The focus of this position is to contribute to the development of next generation manufacturing processes for cell therapies. We are looking for a motivated associate scientist to drive development and characterization projects. | 10/3/2019 |
| 13784 | Bioventus Cincinnati, OH Associate Sales Representative BS/BA Exp: 0-2 years |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Develop and execute regional business plans to achieve quotas for assigned products, which may include cold calling to develop new customers, qualifying and following up on leads and selling to new and/or existing accounts | 10/3/2019 |
| 13785 | Bioventus Chicago, IL Associate Sales Representative BS/BA Exp: 0-2 years |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Develop and execute regional business plans to achieve quotas for assigned products, which may include cold calling to develop new customers, qualifying and following up on leads and selling to new and/or existing accounts | 10/3/2019 |
| 13786 | Merz Franksville, WI Biomedical Engineer - Mechanical BS in mechanical engineering or equivalent Exp: 0-3 years |
This role is to collaboratively partner with business leaders to ensure continuity of supply for MNA device business and optimize our technical service operation to meet the global customer demands. Installed Base Support: Provide continuing product support for manufacturing, regulatory and quality on design requirements, customer needs, testing, CAPA, reliability predictions, and product documentation. etc. | 10/1/2019 |
| 13787 | MSD Rockville, MD Customer Service Representative BS/BA Exp: 1 year |
The Customer Service Representative I will provide professional, courteous, customer-centric service to the MSD customer base. This individual will directly interact with various customers and interface with multiple internal departments to facilitate the processing of quotes, orders and customer requests to allow for timely shipping of MSD products worldwide. etc. | 10/1/2019 |
| 13788 | MSD Gaithersburg, MD Quality Assurance Specialist BS/BA Exp: 1 year |
This Quality Assurance Specialist position is responsible for the operation and compliance of the training program within the Quality Management System (QMS). The incumbent will provide assistance within the department to support Document Control initiatives and the management of document change order packages. etc. | 10/1/2019 |
| 13789 | MSD Gaithersburg, MD Research Associate I BS/MS in relevant field Exp: 1+ years |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. etc. | 10/1/2019 |
| 13790 | MSD Rockville, MD Production Control Tech I BS in a relevant field Exp: 1 year |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. The position will help standardize and improve documentation, manufacturing procedures and processes to increase production efficiency and ensure best practices are followed. The position will also help implement new products, projects and processes within Manufacturing Operations. Some degree of professional latitude, creativity and self-management is expected. etc. | 10/1/2019 |
| 13791 | Microbiologics Saint Cloud, MN Customer Service Representative AS/BA/BS in sales, communication, or related Exp: 1 year |
Essential Responsibilities: Manages incoming calls; respond to customer inquiries and/or direct calls accordingly. Receive and process orders received via phone, email, fax, website, Electronic Data Interchange (EDI) or other type of electronic Purchase Order system; calculates charges and process invoices. Review product availability and order status in the company ERP system (NetSuite). Open customer accounts in NetSuite. etc. | 10/1/2019 |
| 13792 | Micropoint Santa Clara, CA Quality Control Associate MS in chemistry, biology, or related Exp: None needed |
We are looking for highly motivated QC Associates (two openings) to join our quality team. These positions are responsible for participating as team members in a laboratory environment for finished product/or development programs focused on the goal of testing and releasing the immunoassays found in Micropoint's in-vitro diagnostic products for point-of-care (POC) testing. etc. | 10/1/2019 |
| 13793 | Micropoint Santa Clara, CA Manufacturing Operator HS diploma Exp: 0-2 years |
There are two openings. These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the company's disposable test cartridges. Responsibilities: Follow written procedures for set-up, operation, and clean up of manufacturing equipments, final assembly, and packaging. Responsible for manual tasks including, pipette solution, pouch and box labeling, product inspection. Prepare materials used in the cartridge production process. etc. | 10/1/2019 |
| 13794 | MicroVention-Terumo Aliso Viejo, CA Industrial Engineer I BS in industrial, mechanical or related engineering field Exp: 1-3 years |
The Industrial Engineer I supports manufacturing of products for medical devices with work including operational systems development, process flow, operational needs and process efficiencies. Capacity analysis, Layout management, Systems support, Lean programs and Improvement projects are part of the daily activities. Job duties: Analyzes Capacity for production lines including time studies and line balancing.Develops Lean Manufacturing initiatives. Designs and develops operational systems processes for new products, product changes and enhancements. etc. | 10/1/2019 |
| 13795 | MicroVention-Terumo Aliso Viejo, CA Assembler II (1st Shift) HS diploma or equivalent Exp: 1-3 years |
Performs the assembly or sub-assembly of medical devices and products in an advanced position under moderate supervision from line leaders and supervisors in accordance with manufacturing documents and verbal instructions. Using written and verbal instruction to assemble and package product. Records data associated with the building of product on builds records. Ability to meet quality standard. Perform job function within production standard on 2-5 operations. Work with engineers and supervisors to perform special assembly requests | 10/1/2019 |
| 13796 | MicroVention-Terumo Aliso Viejo, CA Engineer I/II, Process Development (with Mechanical Emphasis) BS in engineering Exp: 0-6 years |
This position will lead efforts in the creation and development of new tooling, equipment and fixtures for R&D of medical device products and mfg. processes. Provides mechanical design concepts for automated and semi-automatic equipment and machinery aimed at improving mfg. productivity, capability, and quality. Supports process development activities of new equipment/fixtures/tooling by performing tests to prove that product subassemblies or finished products meet requirements. Works proactively on projects to carry design concepts through to production release and implementation. etc. | 10/1/2019 |
| 13797 | MicroVention-Terumo Aliso Viejo, CA Engineer I/Engineer II, Mfg. Process BS in related field Exp: 0-3 years |
The Engineer I/Engineer II, Manufacturing Process is responsible for the improvement, sustaining, development, and overall support of new and existing manufacturing processes for new and existing products, product changes and enhancements, as well as related tooling and fixtures. Supports validation of product, equipment and processes. Interfaces with other departments to solve production problems. Monitor equipment maintenance program. Investigation and testing of product processes. etc. | 10/1/2019 |
| 13798 | MicroVention-Terumo Aliso Viejo, CA Scientist I BS in chemistry Exp: 0-2 years |
Under guidance and supervision, evaluates the chemical and physical properties of various organic and inorganic substances in order to investigate their applications to the medical device industry. Job duties: Primary work location is in the R&D chemistry laboratory. Secondary work location is in an office environment. Handles chemicals safely in accordance with approved processes and procedures. Performs laboratory tasks under direct supervision. etc. | 10/1/2019 |
| 13799 | MRIGlobal Charlottesville, VA Molecular Biologist BS/BA in biology or related discipline Exp: Entry level |
Our laboratory located in Charlottesville, Virginia is looking for an entry level scientist to work in a microbial forensics laboratory. This staff member will become an integral part of our team receiving vital experience with research, sample preparation and analysis, while gaining a thorough understanding of relevant federal regulations, QA/Safety/SOPs, and instrumentation. Conducts technical tasks and laboratory experimentation under general supervision using established or project-specific protocols and SOPs. etc. | 10/1/2019 |
| 13800 | MRIGlobal Kansas City, MO Veterinary Technician AS/BA/BS Exp: None needed for college candidate |
Job duties will include, but are not limited to animal husbandry, performing technical activities as directed by the study protocol, assisting with ensuring that equipment and supplies necessary to conduct these studies are available, and working in a team environment to conduct studies in conventional and containment laboratories. Specific tasks assigned typically depend upon the needs of the Division and the training and experience of the individual. | 10/1/2019 |
| 13801 | Biomerieux St. Louis , MO Engineering Technician Technical degree Exp: 0-2 years |
Provide technical support to operations engineering and instrument manufacturing with responsibilities specific to printed circuit board assemblies (PCBAs), mechanical assemblies, assembly fixtures, and test equipment. Assist engineers in projects related to manufacturing and electronic test devices used in the production and functional qualification of In vitro diagnostic laboratory equipment. Support and sustain instrument manufacturing activities and facilitate efficient operations within the production environment, optimize existing processes and ensure established production processes are achieved. | 9/29/2019 |
| 13802 | Biomerieux St. Louis , MO IRC Technician - Instrument Refurbishment Center AAS in electronics discipline Exp: 0-3 years |
Perform evaluation, refurbishment, assembly, alignment and acceptance testing of automated electro-mechanical biological test systems on an advanced level while maintaining stock levels. | 9/29/2019 |
| 13803 | Biomerieux Philadelphia, PA R&D Technician BS Exp: 1-2 years relevant experience |
Contributes, with technical and scientific expertise, to the design and development of differentiated, high quality products on time, within budget, and with a high degree of customer satisfaction. | 9/29/2019 |
| 13804 | Bio-Rad Dalas, TX Field Service Engineer I BS in electronics/engineering Exp: 1 year |
Provide customer site service on all LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. Act as customer advocate to ensure satisfaction and repeat business. Maintains company assets including parts inventory and leased vehicle. Administrative duties include service documentation consistent with FDA regulations. Other duties include accurate expense reporting and timekeeping.Must maintain learning plan in training database and regular product update training. Travel is required. | 9/29/2019 |
| 13805 | Bio-Rad San Diego or Los Angeles, CA Proteomics Sales Specialist I BS/BA Exp: 1-3 years sales experience |
Develop and Execute a Territory Sales Plan. Promote and Sell the Bio-Rad Proteomics Portfolio to Achieve the Territory Sales Goals. Build, Manage and Grow Sales Opportunity Funnel. Utilize Various Bio-Rad Departments (Technical Support, Customer Care, Marketing and other Bio-Rad Personnel) In Order to Ensure Complete Customer Satisfaction. Proactively Communicate with Regional Manager on Activities, Market Trends, Opportunities and Forecast. | 9/29/2019 |
| 13806 | LGC Alexandria, MN Laboratory Technician I AS/AA in sciences Exp: 0-2 years |
The Laboratory Technician is an integral part of the Laboratory Operations team and through collaboration with others is responsible for executing the objectives of the Research and Development group. This position will be involved in conducting lab experiments as assigned and be responsible to accurately document results. The Laboratory Technician may be asked to assist in preparing standard laboratory procedures, keep detailed record of experiments, and will report on project results to relevant stakeholders. The Laboratory Technician is expected to be familiar with the scientific background and literature relevant to the projects they are engaged. The work of a Laboratory Technician is directed and evaluated by a senior R&D laboratory member. | 9/29/2019 |
| 13807 | LGC Charleston, SC QC Chemist ( BS Exp: 1 year in production |
This is a QC chemist position where one is responsible to make check standards, routine instrument maintenance and operation of GC/MS, GC/FID, HPLC, and UHPLC/MS, validating manufactured products in a timely manner. Attention to detail, teamwork, the ability to thrive in a fast-paced work environment and organizational skills are necessary to excel in this position. | 9/29/2019 |
| 13808 | Biomerics Salt Lake City, UT Product Development Engineering Technician AS/AA in technical field Exp: 0-3 years |
The Product Development Engineering Technician assists with engineering activities and performs tasks associated with those activities, including developing test methods and fixtures, conducting engineering studies, building prototypes, and other activities associated with the development of medical devices. The Product Development Engineering Technician must be able to work in a team oriented, fast paced environment. Biomerics is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce | 9/29/2019 |
| 13809 | Brooks Indianapolis, IN Facilities Technician I HS Diploma/GED Exp: 0-1 years in mechanical inclined experience |
The Facilities Technician I will be involved with freezer calibrations, freezer scrapping, dipping tanks as well as any other entry-level facility technician duties as required. Specific departmental duties as set forth in the task list and/or departmental training check lists including but not limited to: Perform weekly, monthly, and quarterly freezer maintenance. Responsible for general cleaning duties for the facility which includes cleaning the warehouse floor and maintaining general appearance of inventory items and storage units. Ability to perform aspects of CMMS and Calibration processes. Accountable for completing all necessary documentation in an appropriate manner. Accountable for following all established safety and universal precautions guidelines and procedures. Maintains training file and required documentation. Pro-actively communicates all issues to appropriate personnel. Operate industrial equipment as needed (Forktruck, Scissor lift, etc.). All other duties as assigned. | 9/29/2019 |
| 13810 | Brooks Chelmsford, MA Manufacturing Engineer MS in engineering Exp: 1+ years |
Provides technical and engineering expertise to the Brooks Automation Manufacturing Engineering team in enhancing the design and implementation of our Robotics production area. Candidate must be proficient and hands on in applications of LEAN principles such as DFT (Design Flow Technology), Value Stream mapping, and 5S, in addition to concepts in 6 Sigma statistical reviews of processes in an electro-mechanical environment. | 9/29/2019 |
| 13811 | Brooks Chelmsford, MA Technical Writer MS Exp: 0-1 years |
Creates, develops, organizes, plans, writes and edits operational, maintenance, test, and other electronic or printed publications on company products. Researches engineering schematics, technical design specifications, diagrams and specifications with design engineers, users, and other staff. Helps coordinate the layout and manual organization. Acquires and organizes basic source material, including applicable specifications, engineering write-ups, and drawing packages. May document processes and specifications. Recommend effective formats, produces products that conform to company standards. | 9/29/2019 |
| 13812 | Berg Framingham, MA Research Associate II – Neurology BS or MS in biology, neuroscience, biochemistry or related Exp: 1-2 years in lab setting |
Research Associate II is an experienced and motivated individual. The RA II will characterize novel therapeutic targets for neurodegenerative diseases and assists in the development of potency assays and phenotypic screens in vitro. | 9/28/2019 |
| 13813 | Berg Framingham, MA Laboratory Operations Specialist I AS or BS Exp: 0-2 years |
The Laboratory Operations Specialist I, in the Bioanalytical division, is an entry-level Laboratory Operations Specialist who will work primarily in our lab and they will be accessioning clinical samples, following SOPs, documenting all work performed and will assist with QA tasks. | 9/28/2019 |
| 13814 | BGI Montreal , Ca Lab Technician BS/BA in molecular biology or related Exp: 1-2 years industry expereince/training |
As a member of the BGIA Support team, the position will support next generation processes for genome sequencing. The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. | 9/28/2019 |
| 13815 | BGI San Jose, CA Lab Technician BS/BA in molecular biology or related Exp: 1-2 years industry expereince/training |
As a member of the BGIA Support team, the position will support next generation processes for genome sequencing. The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. | 9/28/2019 |
| 13816 | BioAssay Systems Hayward, CA SALES ASSOCIATE HS Diploma/GED Exp: No experience required |
The Sales Associate will be responsible for processing orders, preparing shipping documents, and keeping detail records. The individual will have to communicate with our customers by phone, fax and e-mail. The position will also involve packaging products for shipment. | 9/28/2019 |
| 13817 | BioAssay Systems Hayward, CA RESEARCH ASSOCIATE - MANUFACTURING BS/BA in chemistry/biology or related Exp: 1-2 years lab experience preferred |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing and packaging the finished products. This candidate may also join part time in our R&D team. | 9/28/2019 |
| 13818 | BioAssay Systems Hayward, CA RESEARCH ASSOCIATE - ASSAY DEVELOPMENT BS/BA in chemistry/biology or related Exp: 1-2 years lab experience preferred |
We are currently looking for an enthusiastic research associate to join our R&D team. This position will entail developing novel assays kits and performing service projects. This candidate may also be involved in manufacturing or providing technical support to customers. | 9/28/2019 |
| 13819 | Bioclinica Princeton, NJ Pricing & Proposals Associate BS/BA Exp: 0-1 years in pharma/CRO |
Generates, analyzes, and manages accurate and timely client proposals by: Reading, analyzing, and collaboratively working with the functional team owners to understand client’s Request for Proposal (“RFP”) & protocol. Validating pricing model is within acceptable company gross margin standards, escalating to Business Lead if outside margins. Consulting on standard, variable, and value-add costing parameters based on RFP and protocol. | 9/28/2019 |
| 13820 | Bioclinica Tranklin, TN Procurement Associate Associates/Bachelors degree in business management or related Exp: 1-2 years vendor interaction |
The Procurement Associate will work directly for the Procurement Manager to assist in the operational procurement at the departmental level. He/She will own the procurement process for the department in scope and ensure compliance, budgets and corporate strategy. He/She will have responsibility for negotiating pricing arrangements. He/she will work closely with the finance, accounts payable, legal, and quality control. | 9/28/2019 |
| 13821 | Bioclinica Princeton, NJ Imaging Operations Coordinator Associates/Bachelors in engineering, information technology, or computer science Exp: 1 year computer experience |
TheImagingOperationsCoordinator performs data processing for allstudies. Review,process,trackand monitor alldata received from clinicalsites. Verify upon login that data received istheexpected data based on project protocol and previouspatientidentifiers. Review data discrepancies and resolve or route to study team as necessary/. et. | 9/28/2019 |
| 13822 | Bioclinica Princeton, NJ DXA Imaging Analysis Technican I BS/BA in health/sciences Exp: 0-1 years in clinical trials support |
Performs DXA analysis and quality control in accordance with study-specific deliverables and within study-specific turnaround times. Understands functions of software used to produce and collect DXA image analysis results. Communicates with Clinical Project Managers, Imaging Research Associates and/or Scientific Director regarding image quality, deliverables, and data discrepancies. | 9/28/2019 |
| 13823 | Biocytogen Boston, MA in vivo Pharmacology Research Associate BS or MS Exp: 1-5 years research experience |
Perform preclinical pharmacology studies in rodents. Tasks include drug administration via multiple routes (IV, IP, SC, PO etc), blood and tissue collection, and tumor volume measurement. Experience with small animal surgery is a plus. Communicate and coordinate with other scientists on project team to draft, finalize, and implement study protocols. Follow protocols and independently execute tasks. Collect and record data. Prepare summary of experimental procedures and results and present data in team meetings. | 9/28/2019 |
| 13824 | Biodesix Boulder, CO Test Support Specialist I HS Diploma/GED Exp: 1-3 years customer service/data entry |
Test Processing Support Specialist 1 duties will consist of accurately and precisely transferring and entering data from test request forms into an electronic data base. Confirmation of entered data, and confirmation that data provided meets the minimum requirements as indicated by the QMS. Timely and accurate delivery of reviewed test results. | 9/28/2019 |
| 13825 | Biodesix Boulder, CO Laboratory Technician BS/BA in chemistry/biological sciences Exp: 0-2 years lab training |
Laboratory Technicians must have the technical training and experience required to perform regulated clinical laboratory testing, including sample accessioning and processing using standard in-vitro laboratory techniques which include DNA and RNA extraction from whole blood, ddPCR (digital droplet PCR), Mass Spectrometry for proteomic testing and to operate a proprietary LIMS. | 9/28/2019 |
| 13826 | Bioduro San Diego, CA Quality Assurance Associate – Analytical & Manufacturing Support BS/BA in science Exp: 6-12 months in pharma/lab |
The Senior Quality Assurance Associate assists in execution of systems to assure cGMP compliance for all relevant operations carried out within and for BioDuro, LLC. This function includes: Analytical Support – Support functions include, but are not limited to: review and approval of in-process testing, release testing of products, stability testing, other data summaries, method validation data, laboratory equipment validation protocols, product certificates of analysis, generation of environmental chamber monitoring reports. Other duties as deemed appropriate by Head of Quality. | 9/28/2019 |
| 13827 | Bioduro San Diego, CA Associate Scientist (Analytical Development) BS in chemistry or related Exp: 1-2 years in chemistry lab |
The Analytical Development Associate Scientist facilitates and assists in execution of systems to assure cGMP compliance for all relevant operations carried out within and for BioDuro, LLC. Responsible for performing pharmaceutical formulation sample and finished product analysis testing and basic validation experiments using different analytical instruments (HPLC, Dissolution, and KF) and general laboratory duties. | 9/28/2019 |
| 13828 | Biogen Cambridge, MA Engineer I, Cell Culture Development BS in bio/chemical engineering Exp: 0-2 years |
This position will focus on development of high productivity and robust cell culture processes through classically and statistically designed experiments. The candidate’s goals will be to increase process robustness and productivity through comprehensive understanding of levers important to mammalian cell culture. A major component of the role will involve conducting and documenting laboratory bioreactor experiments with a focus on process definition and understanding, experimental design and troubleshooting, and data analysis. The ideal candidate will be able to work collaboratively with pilot scale and tech transfer teams for execution of development projects. In addition, the ideal candidate will contribute to improving laboratory process workflows, making laboratory work more efficient and with greater impact. | 9/28/2019 |
| 13829 | Biogen Cambridge, MA Associate Scientist II, Alzheimer’s Disease and Dementia Research Unit MS in biological sciences Exp: 1+ years experience |
The successful candidate will have hands-on experience with a variety of in vitro and in vivo models relevant for neurodegenerative diseases and the ability to utilize these models for target validation, mechanism of action studies and support for drug discovery projects as a member of our world class research team in the Alzheimer’s Disease and Dementia Research Unit. As Associate Scientist II, the expectation is that the incumbent is capable of planning and executing experiments in consultation with the supervisor including the analysis and interpretation of the experimental results to achieve agreed upon objectives. | 9/28/2019 |
| 13830 | Biogen Cambridge, MA Associate Scientist I, Technical Development (Development Support) AS/AA or BS/BA in biological/chemical sciences Exp: 1 year in lab environment |
The individual will assist in the development and optimization of formulations and provide technical expertise on preparation procedures and mixing process parameters using both practical and scientific knowledge. Will work as member of dynamic team developing and following established procedures to ensure a consistent service is delivered. Management of department chemical and consumable inventories, ensuring proper levels are available. Frequent collaboration and communication with multiple line functions to develop solution formulations and preparation process instructions. | 9/28/2019 |
| 13831 | Biogen Research Triangle Park, NC Manufacturing Associate BS/BA Exp: 0-2 years work experience |
The Manufacturing Associate performs and documents manufacturing operations in a cGMP environment that involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments. The role will: Execute manufacturing processing steps and/or manufacturing support activities, monitoring the process against the batch record, SLR and control system. May coordinate or lead process steps as requested. Document/Record and Review cGMP data and information (including documentation of deviations) for processing steps and/or equipment activities, following standard operating procedures. Revises or creates documents as instructed. Key documentation includes batch records, SLRs, and equipment logbooks. | 9/28/2019 |
| 13832 | Biolegend San Diego, CA Research Associate- BMIA ELISA BS in chemistry/biology Exp: 0-1 years lab experience w/immunoassays |
This position is responsible for developing immunoassay products in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working closely with an experienced scientist on developing a line of product utilizing ELISA or bead-based immunoassay and flow cytometry technologies. | 9/28/2019 |
| 13833 | Biolegend San Diego, CA Process Development Associate BS/BA in biological/chemical sciences Exp: 1-3 years lab experience w/protein chemistry |
The Process Development Associate will be an integral member of a team that ensures the highest quality of our finalized antibody products. This position offers the opportunity to gain experience with different types of conjugation chemistries and different chromatography methods to purify conjugated antibodies and offers the opportunity to work in small scale to large scale product projects and to learn to utilize the (Enterprise Resource Planning) ERP database to track production schedules and deadlines and to enter production results | 9/28/2019 |
| 13834 | Biolegend San Diego, CA Material Coordinator BS in biological sciences Exp: 1-2 years lab experience preferred |
The Material Coordinator is an entry level role that will support corporate business development efforts to expand company product portfolio through in-licensing, in-house development, and other methods of acquisition. This position will be responsible for documenting, receiving, and distributing incoming materials to stakeholders within the facility and outside locations and will work in a collaborative environment with other internal departments including Finance, Customer Service, Research and Development, Purchasing, Facilities and Quality Assurance. | 9/28/2019 |
| 13835 | Biolegend San Diego, CA Manufacturing Associate - Tissue Culture AS/AA in biological sciences Exp: 6 months |
. This position offers a varied work load and will enable you to gain solid experience that will allow you to grow and increase your skill set within a fast-growing and stable biotech company. This position will also allow you to gain experience in all areas of tissue culture and cross training on a variety of other supporting tasks such as downstream processing, ELISA assays, qPCR, mycoplasma detection, and NOVA BioProfile 400 use and maintenance. | 9/28/2019 |
| 13836 | Biolegend San Diego, CA Research Associate- Biomarker Immunoassay BS in chemistry/biology Exp: 1 year or more w/immunoassays |
The Research Associate will be involved in all aspects of the product development processes including designing, testing, troubleshooting, product transferring and launching. More specifically, he or she will be working closely with an experienced scientist on developing a line of product utilizing bead-based immunoassay and flow cytometry technologies. | 9/28/2019 |
| 13837 | Biolegend San Diego, CA Project Coordinator - Custom Solutions Team BS in life sciences Exp: 1-3 years in biotech/pharma |
The CST Project Coordinator will handle internal project coordination for our custom solutions team and contribute BioLegend’s mission of providing legendary customer service. They will be accountable for their own project pipeline, from the initial scoping through to manufacturing and timely delivery to the customer. | 9/28/2019 |
| 13838 | BioMarin Novato, CA Research Assistant / Research Associate at BioMarin BS in pharma sciences/biochemistry, related Exp: 1-2 years in R&D lab |
The prospective employee will work in the Formulation Development group to assist in the advancement of BioMarin’s therapeutics for clinical evaluation and potential commercialization. The candidate will be responsible characterization drug products, screening of formulation prototypes, evaluating product stability and compatibility with various container closure systems using routine and semi-routine analytical methods under limited supervision. | 9/28/2019 |
| 13839 | BioMarin San Rafael, CA Contracts Associate (TEMPORARY) BS/BA Exp: 0-2 years |
This role will support BioMarin's Legal Department and business partners by drafting, negotiating and tracking a high volume of contracts. Duties include: Drafting, primarily from templates, multiple contract types including Non-Disclosure Agreements, Master Service Agreements, Amendments, Scopes of Work, and Change Orders, using SpringCM, BioMarin's contract lifecycle management system ("SpringCM"). Monitoring and tracking a large volume of contracts from draft to final signatures using SpringCM. | 9/28/2019 |
| 13840 | BioMarin San Rafael, CA Research Associate (TEMPORARY) BS or MS in pharma sciences, biochemistry, or related Exp: 0-2 years lab experience |
The Research Associate I/II, functions to manage, coordinate, and perform activities required for the testing of drug product or human and animal specimens associated with one or more research and pre-clinical studies. In this position the candidate will work closely with Scientists in the Research group focused on mass spectrometry-based assays. | 9/28/2019 |
| 13841 | BioMarin Novato, CA Analyst, QC In-Process BS Exp: 0-3 years lab experience |
The QC In-Process (QCIP) Analyst is responsible for performing microbiological and analytical test methods on in-process intermediates and varying stages of drug products, under minimal supervision and within cGMP guidelines, to support further manufacturing of commercial and clinical therapeutics. This role will involve knowledge that includes but is not limited to the following analyses and concepts: Protein determination by BCA, Bradford, and UV Absorbance, Enzyme activity, Endotoxin detection, Bioburden quantification, HPLC, Total Organic Carbon, microbial identification and challenge studies, aseptic techniques, and method validation. | 9/28/2019 |
| 13842 | BioMarin Novato, CA Analyst, Quality Control BS in biological sciences Exp: 0-2 years lab experience |
The Quality Control Analyst’s main job responsibility is to manage the Quality Control In-Process department documents to ensure their accuracy, quality and integrity. The candidate will organize, maintain, track and archive department documents and records while adhering to the BioMarin's document lifecycle procedures and in accordance with the records retention schedule. The QC Analyst may be required to develop new processes and improve upon the current system to allow retrieval of data records more effectively. Periodically, the QC analyst may be responsible for training employees on records management procedures and policies, which include documentation, retention, retrieval, destruction and disaster recovery. | 9/28/2019 |
| 13843 | BioMarin San Rafael, CA Clinical Trial Assistant (TEMPORARY) BS/BA in nursing or life/health sciences Exp: 1 year in pharma |
The Clinical Trial Assistant (CTA) performs essential responsibilities for successful trial execution at BioMarin. The CTA assists with the coordination of activities associated with the start-up, management, and close-out of clinical studies under the direction the Clinical Operations team. This may include assisting with study matters that impact study timelines, quality and budget. | 9/28/2019 |
| 13844 | Bausche Health Lynchburg, VA Distribution Associate I HS Diploma/GED Exp: 6 months or more |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader. | 9/25/2019 |
| 13845 | Baxter Round Lake, IL Quality Associate I, Receiving & Inspection AS/AA or BS/BA Exp: 1-3 years in medical devices/pharma |
Quality Associate performs daily quality review of raw material documentation to ensure that materials being received are produced in accordance to Company methodology, procedures, and standards. Quality Associate completes Change Control, Supplier Quality, and Nonconformance and Corrective Action Preventive Action (CAPA) quality records related to Receiving & Inspection. Quality Associate is SME for Receiving & Inspection procedures and manages projects. | 9/25/2019 |
| 13846 | Baxter Opelika, AL QA I -Training BS in sciences Exp: 0-3 years in manufacturing |
Conducts reviews of documentation and reports for conformance to procedures, protocols, and regulatory requirements. Ensures training effectiveness in production. Provide Quality support with assigned projects and/or audits to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (GMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply. | 9/25/2019 |
| 13847 | Baxter Round Lake, IL Associate, TDP BS or MS in engineering/sciences Exp: 0-2 years |
Over the course of two years, the TDP participant will complete four x 6-month rotations, with the option to combine two rotations into a single 12 month rotation. The rotations will be based in Research and Development at Baxter’s Round Lake, IL, and Deerfield, IL, locations. Participants can optionally have the opportunity to travel to or work from other Baxter Research and Development sites across the globe. | 9/25/2019 |
| 13848 | Bayer Creve Coeur, MO Software Developer-Entry BS in computer sciences Exp: Entry Level |
The primary responsibilities of this role, Software Developer, are to: Collaborate daily with a team of Software Developers, Product Manager, Product Specialists, and Agile Coach to build and support applications; Work with team and Product Manager to manage project priorities, deadlines and deliverables; Interact directly with business customers to gather and understand requirements and how they translate in application features; | 9/25/2019 |
| 13849 | Bayer Woodland, CA Lab Tech II BS/BA in science-related field Exp: 1+ years in lab setting |
The primary responsibilities of this role, Lab Technician II, are to: Under the direction of Lab Operations Managers and/or Lab Coordinators complete the testing processes ensuring process control, accurate data management, timely escalation of problem solving, and error correction; Ability to learn and apply scientific methods and non-routine techniques for analysis as directed by protocols and work instructions to deliver quality results - which may include preparation of reagents, media, controls and sample preparation | 9/25/2019 |
| 13850 | Bayer Indianola, PA Engineer Quality BS in engineering Exp: Entry Level |
The primary responsibilities of this role, Engineer Quality, are to: Provide focused quality engineering support to develop, support and maintain quality engineering methodologies that meets Customer, Regulatory and Bayer requirements; Lead the Material Review Board cross-functional team to investigate and address all manufacturing non-conformances; Lead and support investigations by conducting problem solving and root cause analysis to address failures identified by customer complaints, internal non-conformances and manufacturing yields. | 9/25/2019 |
| 13851 | Bayer St. Louis , MO Research Associate MS in plant biology or related Exp: 0-1 year working experience |
Responsible for carrying out routine and discovery experiments in partnership with scientists. Responsible for generating highest quality research data and performing validation experiments; Responsible for organizing and recording experiment notes/best practice documents in a timely fashion to secure the company’s IP and FTO; Manage best practice documents training of new members and help onboard new team members | 9/25/2019 |
| 13852 | Beaufort Norfold, VA Clinical Trial Assistant BS/BA in science-related field Exp: Entry Level |
Beaufort is currently looking for a Clinical Trial Assistant to add to our growing Clinical Operations team! The Clinical Trial Assistant (CTA) is responsible for supporting the clinical project team in daily study activities and clinical trial conduct by providing administration and project tracking support. | 9/25/2019 |
| 13853 | Hach Loveland, CO Entry Level Firmware Engineer BS or MS in computer sciences/engineering Exp: Entry Level |
The entry level firmware engineer is an integral position within the Hach R&D team. The engineer will be part of a fast paced team, working in a collaborative environment that will drive growth and innovation within the firmware competency. The engineer will engage with SCRUM in an Agile team environment with the core responsibility of developing high quality innovative solutions. | 9/25/2019 |
| 13854 | BD Glens Falls, NY Manufacturing Team Member I- Balloon Electrodes HS Diploma/GED Exp: No prior experience required |
Performs any combination of tasks involved in the manufacture and assembly of medical devices. Responsible for following safety policies and procedures. Perform a variety of duties to assemble all types and sizes of product, components, and sub-assemblies using a variety of standard and specialty assembly machines or hand operations. May be required to press, bond, solder, flare, strip, clamp, sand, weld, mount/takedown or inspect for appearance, gauging of parts by “no-go” or “go” gauges and set fixtures. | 9/25/2019 |
| 13855 | BD Baltimore, MD Machine Operator 1 HS Diploma/GED Exp: 1 year manufacturing/warehouse experience |
Performs routine set up, operation, preventative maintenance (PM) and reports troubleshooting of basic manufacturing equipment via manual or semi-automated means. Controls and adjusts machine settings. Inspects in-process parts to ensure consistent quality and removes defective product, packaging, and component material. Assists with root-cause analysis activities for process or product exceptions. Identifies and escalates any issues associated with the machine performance and/or product quality. | 9/25/2019 |
| 13856 | BD Tempe, AZ R&D Engineer II, EU MDR MS in engineering Exp: 1-3 years |
This position must have a working knowledge of the design process and documentation for US, EU and OUS product launches. This position reviews the DHF for released products with regard to compliance to EU MDR, determine gaps, and develops mitigation plans and completes mitigation. This position is responsible for conducting engineering protocols and reports for product qualification and validations. This position should have working knowledge of New Product Development process, including design, development and implementation of new products, processes, test methods and equipment. | 9/25/2019 |
| 13857 | BD Zelienople, PA Service Technician AS/AA in electronic engineering Exp: 1-2 years |
The Service and Repair Technician is responsible for troubleshooting, disassembly, testing, and assembly of electro-mechanical medical devices. All service work performed must be clearly documented in the approved Service/Complaint Handling System (TrackWise). Works from documented procedures, work instructions, engineering drawings, or sketches as defined in the Bard Electronic Systems (BES) Quality System. | 9/25/2019 |
| 13858 | Cepheid Bothell, WA Oligo Manufacturing Associate BS in sciences, chemistry preferred Exp: 0-2 years |
The Oligonucleotide Production Associate will perform tasks associated with the production of oligonucleotides in a dynamic fast paced GMP manufacturing environment. The associate will also be required to provide support by maintaining inventory and buffer preparation. | 9/25/2019 |
| 13859 | Leica Biosystems Richmond, IL Shipping Associate HS Diploma/GED Exp: 6 months + in warehouse |
This role has a direct impact on Inventory Accuracy and Productivity. High volumes and fast paced physical activity throughout most of the day characterize this role. Responsibilities include: Completion of all assigned warehouse duties within designated productivity rates. Completing all Safety Audit | 9/25/2019 |
| 13860 | Cepheid Sunnyvale, CA Systems Support Engineer MS in engineering/electronics/IT Exp: 0-2 years |
The Systems Support Engineer is responsible for providing advanced product support to customers requiring assistance with instrumentation, software and hardware components sold and distributed by Cepheid. As a member of the Tier 2 Technical Support Team, you provide product support to internal and external customers via phone, email and web serving as the technical expert in Cepheid’s Customer Care experience. | 9/25/2019 |
| 13861 | Mallinckrodt Pharmaceuticals Hobart, NY Manufacturing Assoc. I - 2nd Shift HS diploma or equivalent Exp: 3-12 months |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. etc. | 9/24/2019 |
| 13862 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - 4on/4off (C) Shift 6pm-6am HS diploma or equivalent Exp: 3-12 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. etc. | 9/24/2019 |
| 13863 | Mammoth Biosciences San Francisco, CA Research Associate BS/MS in biology, chemistry, or related Exp: 1+ years |
Mammoth is seeking a Research Associate experienced in protein and nucleic acid biochemistry techniques to support our research and product development teams. The ideal candidate will have experience with in vitro assay development, nucleic acid extraction and amplification techniques. Further, the candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. etc. | 9/24/2019 |
| 13864 | McGuff Pharmaceuticals Santa Ana, CA Manufacturing Technician - Evening Shift BS Exp: 0-3 years |
Duties Include: Operation of pharmaceutical manufacturing equipment including automated aseptic fill lines, washers, ovens, and autoclaves. Responsible for set-up, adjustments, sanitization, minor maintenance, and operation of all machinery in the sterile filling area. Experience in using aseptic technique to conduct aseptic filtration and filling of finished product. etc. | 9/24/2019 |
| 13865 | McGuff Pharmaceuticals Santa Ana, CA Microbiology Technician BS Exp: 0-5 years |
The Microbiology Technician will be responsible for (1) Verifying that materials and products comply with microbial and/or chemical specification limits (2) Conducting laboratory testing in support of operations, (3) Maintain the laboratory operations in compliance with McGuff policies, federal regulations, state regulations, and international standards, (4) Maintain documentation, calibration, and validation of all microbial equipment, (5) conduct other duties as assigned by the laboratory supervisor and/or Microbiologist. etc. | 9/24/2019 |
| 13866 | McGuff Pharmaceuticals Santa Ana, CA Manufacturing Techician unspecified Exp: 0-3 years |
Duties include: Operation of pharmaceutical manufacturing equipment including automated aseptic fill lines, washers, ovens, and autoclaves. Responsible for set-up, adjustments, sanitization, minor maintenance, and operation of all machinery in the sterile filling area. Experience in using aseptic technique to conduct aseptic filtration and filling of finished product. etc. | 9/24/2019 |
| 13867 | MS Biosciences Oakdale, MN Quality Assurance Specialist BS Exp: 1-2 years |
This person will be responsible for assisting in the maintenance and function of the quality management systems at MD Biosciences. This person should have a background in and knowledge of quality systems in a laboratory setting and preferably have experience in aCLIA &/or GLP-regulated environment. etc. | 9/24/2019 |
| 13868 | Medicomp San Francisco, CA Cardiac Monitoring Technician HS diploma Exp: 1+ years |
Looking for an ECG interpreter, for our San Francisco, CA office, who is excited about having the front line responsibility of triaging the patients who have our life-saving products prescribed to them. That's right, I said Life-saving! This is only going to happen one way you have to have a solid work ethic and be able to focus on the clinically significant signs and symptoms of one or more patients while in a noisy environment that is full of interruptions. etc.. | 9/24/2019 |
| 13869 | Merck Millsboro, DW Technician, Animal Care HS diploma/AS in relevant field Exp: 1+ years |
An Animal Care Technician is responsible for the care and husbandry of animals. Technicians will work with a variety animal species. At all times, technicians must follow Standard Operating Procedures, adhere to all safety and company policies and perform duties assigned by department supervision. etc. | 9/24/2019 |
| 13870 | Merck Millsboro, DW Senior Technician, Operations BS in a biological life science Exp: None needed for BS candidate |
Objective of position: At all times technician must follow GMP and SOP and adhere to all safety and company policies while performing more advanced laboratory services in various manufacturing areas. Job Summary: Position Description: Sr. Tech is multi-skilled within own product/department and develops skills in multiple products/departments. Multi-skilled within own product/department. etc. | 9/24/2019 |
| 13871 | Merieux NutriSciences Minnetonka, MN Microbiology Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 13872 | Merieux NutriSciences Minnetonka, MN Microbiology Technician - 2nd Shift unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 13873 | Merieux NutriSciences Stone Mountain, GA Microbiology Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 13874 | Merieux NutriSciences Gainesville, FL Chemistry Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 13875 | Merieux NutriSciences Columbus, Oh Lab Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 13876 | Merieux NutriSciences Crete, IL Chemist I unspecified Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food sample. The incumbent analyzes the concentration of certain components in food sample. The incumbent must accurately prepare and process the sample to obtain the needed results. etc. | 9/24/2019 |
| 13877 | Merieux NutriSciences Allentown, PA Receiving Tech unspecified Exp: Entry level |
Mérieux NutriSciences is a leader in food science and testing technology. With over 6,000 employees working in 80 labs in 21 countries, our team will stop at nothing to make sure consumers around the world are protected from foodborne illness and pathogens. Each member of our team plays a critical role in our mission. We are currently seeking a Lab Assistant to provide assistance to our technicians and scientists. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 13878 | Mapp Biopharmaceutical San Diego, CA Research Assistant – Cell Line/Cell Culture Development AS in a relevant scientific or engineering field Exp: 1 year |
Responsibilities: Routine maintenance of mammalian cell cultures. Executes basic protein analysis assays (SDS-PAGE, ELISA, Octet etc.). Prepares buffers and solutions to support cell culture and protein analysis assays. Assists in bioreactor set-up and operation for antibody production and harvest. etc. | 9/24/2019 |
| 13879 | MasterControl Salt Lake City, UT QA Software Engineer AS/AA Exp: 1-2 years |
MasterControl is looking for a creative and energetic test engineer to join our Digital Experience Team. This new team member will use innovative testing tools and methods to help make the MasterControl web experience a best-in-class experience. We are looking for a passionate, self-starter with a knack for uncovering issues and a willingness to switch context and change direction based on business needs. We are a small team that does big things. etc. | 9/24/2019 |
| 13880 | Masy Bioservices Pepperell, MA Field Calibration Technician II HS diploma/AA/AS Exp: 1-3 years |
Perform routine calibration and preventive maintenance of Masy and customer equipment. Calibration may include temperature, relative humidity, CO2, voltage, pressure, time, rotation, etc. following documented procedures using precision standards. Calibrations will be performed in-house and at customer sites. Create, modify and execute calibration procedures and calibration certificates. Perform testing to support the quality management system and report, troubleshoot and make recommendations about quality issues relating to calibration. etc. | 9/24/2019 |
| 13881 | Masy Bioservices Pepperell, MA Biorepository Operations Technician HS diploma or equivalent Exp: 1-2 years |
This position is responsible for storage of customer products requiring specific environmental conditions. Duties involve cleaning, couriering, shipping, receiving and inventorying. Abide by area work instructions to ensure customer product is stored appropriately and moves to/from customer and to/from Masy with appropriate controls. Accuracy, attention to detail and GMP compliance are key requirements. etc. | 9/24/2019 |
| 13882 | Masy Bioservices Hatfield, PA Validation Engineer I BS/BA in relevant technical or scientific field Exp: None needed for BS/BA candidates |
Responsibilities for this position involve validation equipment preparation, protocol execution and final report generation. This position will support a wide range of validation activities focused on environmental chambers, including: cryo-freezers, cold rooms, refrigerators, incubators, sterilizers, depyrogenation ovens, stability chambers, warehouses, etc. etc. | 9/24/2019 |
| 13883 | Masy Bioservices Pepperell, MA Monitoring Systems Technician AS in technical or scientific field Exp: 1-2 years |
Responsibilities for this entry level position involve preparation, installation, and support for monitoring systems for both external customers and internal system usage. Duties/responsibilities: Travel to project sites to assist with start-up, integration, and validation services. Resolve customer issues or difficulties in a manner that is consistent with the company mission, values and financial objectives. Prepare monitoring system equipment. etc. | 9/24/2019 |
| 13884 | Arsenal Medical Boston, MA Chemical Engineer/Materials Scientist I BS in chemical engineering/chemistry or related Exp: 0-3 years |
We have an opening for a recent graduate with experience in chemical engineering or polymer and material science to join our team. This position will be hands-on, laboratory based, and will support projects developing novel in-situ forming medical devices. Duties include: Collaborate closely with a multi-disciplinary team of scientists and engineers to develop chemical formulations. Identify, develop, and perform characterization bench test methods enabling material and formulation evaluation. Properly document experimental procedures, designs, and results in a laboratory notebook, conduct data analysis, and present experimental data in meetings | 9/22/2019 |
| 13885 | Arthrex Ave Maria, FL Manufacturing Engineer I - Distal Extremities BS/BA in engineering or related Exp: 0-4 years |
Working as Manufacturing Engineer - Distal Extremities, you will responsible for supporting Engineering Manager with all support for the life cycle development of Class I, II and III medical devices, including new product development and maintenance of released products. This includes design, develop, implement and improve manufacturing processes to produce cost effective quality medical device products and systems. Provide manufacturing engineering expertise to create, document and implement required procedures and documents. Excellent analytical and communication skills, understanding of manufacturing and a Bachelors’ degree in Engineering or Engineering Technology will be essential for this position. | 9/22/2019 |
| 13886 | Arthrex Sandy Springs, SC Engineer Tech - Manufacturing AS/AA in engineering technology Exp: 0-2 years |
Support the development, implementation and improvements of manufacturing processes to produce cost effective quality products. Successful candidates for these positions will have a solid CNC Machining background, including experience with the setup, operation and troubleshooting of mills and/or Swiss lathes. Up to 5-axis machining experience is desired. The successful candidate for this position must be willing to attend initial training in the Naples, FL area if/as needed by Arthrex. | 9/22/2019 |
| 13887 | ArunaBio Athens, GA Research Associate I – Preclinical R&D Team BS/BA in biological sciencecs Exp: 1-2 years lab experience |
The Research Associate I supports the R&D efforts of ArunA Bio by aiding in the development of novel exosome therapies for a number of neurological diseases. This position must work collegially as a part of a larger team and requires the individual to carry out complex tasks. We are seeking a biologist with in vivo research experience. The successful candidate would participate in a wide variety of research activities including animal care, animal technical procedures, animal health evaluations, and research data collection. | 9/22/2019 |
| 13888 | Priamal Riverview, MI Quality Assurance Specailist I - Manufacturing BS/BA in physical/biological sciences Exp: 0-3 years in pharma operations |
The Specialist will directly support the implementation, execution, and maintenance of Quality Systems related to manufacturing to ensure the PPS-Riverview site complies with regulatory requirements as propagated by the United States Food and Drug Administration (USFDA) and other international regulatory authorities. Principle assignments related to compliance may include material release, review and implementation of new and revised documentation to support PPS-Riverview Quality Systems and operations, internal audits, and training of site personnel to meet Good Manufacturing Process (GMP) requirements. The scope of this position will support both clinical and commercial manufacturing, as well as process development, in the Riverview facility. | 9/22/2019 |
| 13889 | Myriad Genetics Salt Lake City, UT Training Specialist BS/BA in engineering or related Exp: 0-3 years |
The Training Specialist I, Prod-Ops Support administers the training program, ensuring that employee training needs are defined and met. This position works with Training Power Users and end users to ensure that job appropriate training is available and completed. Maintain training that meets all departmental needs and follows regulatory requirements for training and competency. Develop training materials for lab processes. Create a variety of training programs including e-training, computer-based, lecture, and other training formats. | 9/22/2019 |
| 13890 | Myriad Genetics South San Francisco, CA Manufacturing Associate BS in biological sciences/molecular biology Exp: 0-2 years in cGMP molecular biology |
The Manufacturing Associate is responsible for following established protocols to regularly manufacture reagents for use in the production laboratory, as well as assist in implementing upgrades to improve the quality and efficiency of manufacturing protocols and processes. They will also create, edit, and review SOPs, train junior staff, and play a key role in process scaling efforts. | 9/22/2019 |
| 13891 | Myriad Genetics Salt Lake City, UT Laboratory Technician BS or MS in biological/physical sciences or engineering Exp: 0-2 years |
The Laboratory Technician is responsible for specimen processing, testing and monitoring test performance. The technician must demonstrate competency, as defined in the department’s training program, prior to performing independent testing. This position will work with department management and quality team members to ensure that laboratory activities are defined, documented and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation and continuous improvement projects. | 9/22/2019 |
| 13892 | AstraZeneca Frederick, MD Quality Control Analyst - Operations BS/BA in sciences/biotech/pharma Exp: 0-5 years |
Performs selected quality control testing activities, dependent upon assigned area, including the following: Responsible for conducting raw materials, in process, finished product and stability testing according to standard operating procedures. Completes appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms. Supports preparation of validation protocols, executes experiments, and provides data for validation reports. | 9/22/2019 |
| 13893 | Asuragen Austin, TX Quality Assurance Specialist I AS/AA 2- year program Exp: 6 months to 1 year |
The Quality Assurance Specialist I is responsible for helping to ensure compliance with QSR, MDSAP, ISO, GLP, and CLIA as they relate to Quality Assurance activities in Asuragen’s manufacturing facility. Provide Quality Assurance support to the Operations department with a focus on production. This is achieved though the following key duties: Develop working knowledge of quality system processes and apply this knowledge to support manufacturing operations. Assist in the management of historical files for manufactured products, including archived records stored on and off site | 9/22/2019 |
| 13894 | Alphatech Carlsbad, CA Regulatory Affairs Coordinator BS/BA in life science/engineering Exp: 1 year in research |
Maintains regulatory databases, license approvals, user fees, certificates, and establishment registrations. Submits Unique Device Identification and labeling data to regulatory agencies using various third-party applications. Responsible for post market surveillance evaluation, trending, and reporting including updates to risk management (FMEA) process.Assists in developing, maintaining, assigning, and tracking company Standard Operating Procedures (SOPs) to ensure compliance with applicable global regulatory requirements. | 9/22/2019 |
| 13895 | Alphatech Carlsbad, CA Material Handler HS Diploma Exp: 1-3 years in inventory |
Under routine supervision, this position is responsible for creating purchase orders and shipping inventory for outside processing. Counts and verify parts for outside processing. Packages parts safely for shipping. Creates purchase order for outside processing. Assists with cycle counts on raw materials, components, and distribution when needed. Conforms to all company policies and procedures and perform all duties in compliance with applicable FDA and state regulations as well as standards including but limited to ISO 13485. | 9/22/2019 |
| 13896 | Alphatech Carlsbad, CA Regulatory Affairs Specialist BS/BA in life science/engineering Exp: 1 year in FDA environment |
Collaborates as a core team member on new product development teams. Determines and documents appropriate regulatory strategy for proposed new products. Supports design control activities. Prepares regulatory submissions including 510(k) premarket notifications for US FDA. Prepares regulatory submissions including technical files/design dossiers for registration of products in European Union and interfaces as needed with Notified Bodies regarding significant changes to products. Evaluates design changes to products to determine impact to submissions and potential need for additional submissions. | 9/22/2019 |
| 13897 | Atreca South San Francisco, CA Research Associate I, In Vitro Pharmacology BS in biology or related Exp: 1-2 years in cell line research |
Oversee the growth and inventory of tumor cell panels needed for primary and secondary screens. Provide assistance with carrying out binding screens against tumor cell panels. Share and present data to team members. | 9/22/2019 |
| 13898 | AtriCure Cincinnati, OH Clinical Operations Associate HS Diploma Exp: 1-3 years in finance/accounting/admin |
The Clinical Operations Associate position will be a key contributor to AtriCure’s clinical affairs department to assist in the development, implementation, and execution of multiple key study functions. The Clinical Operations Associate primary responsibilities include but are not limited to device supply logistics, financial processes (contracts, budgets, and invoices), essential documents, trial master file (TMF), and select monitoring activities. Responsibilities will vary by study. | 9/22/2019 |
| 13899 | Boston Scientific Maple Grove, MN Machine Operator I AS/AA technical degree preferred Exp: 1 year grinding, extrusion, molding, branding operations |
Primary focus is to build quality product by following processes to meet all production goals. Responsibilities include: Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Under the direction of other maintains accurate records such as Manufacturing Execution System (MES), Shop Floor Paperwork (SFP), training Records System (TRS), Product Data Management (PDM), Systems Application & Products (SAP) and Process Equipment Optimization (PEO). | 9/22/2019 |
| 13900 | Boston Scientific Marlborough, MA Analyst I, Compliance Communications & Training Job HS Diploma Exp: 1-4 years in training/communication |
The Compliance Analyst for Global Compliance Training and Communications will be responsible for implementing and maintaining components of a comprehensive compliance training and communication program. Ideal candidates will have strong analytical, verbal and written communication and project management skills and understand risks related to regulations applicable to the medical device industry (e.g. the anti-kickback statute, Foreign Corrupt Practices Act, etc.). | 9/22/2019 |
| 13901 | Boston Scientific Coventry, RI Process Engineer I Job BS in mechanical/chemical engineering Exp: 0-2 years |
The Process Engineer I is responsible for developing and maintaining capable processes and ensuring efficient and effective sterilization operation. This person will provide problem-solving skills to enable sterilization innovation while using technical and collaboration skills alongside his/her passion for innovation and continuous improvement to drive growth through efficient and effective process improvements. | 9/22/2019 |
| 13902 | Boston Scientific Valencia, CA Product Analyst I Job HS Diploma minimum Exp: 1 year in regulated environment/document processing |
In this role you will work closely with Patient Care and the Complaint Call Center areas to process all customer issues and identify complaints, as required by FDA, Canadian, European, and other International regulations related to medical device manufacturers. Maintain all complaint files in accordance to Boston Scientific policies. The position will support post market and clinical studies. Must be able to work well in a team environment, foster team building, proactively communicate project and task status, and operate with a high level of initiative. Possess verbal and written communication skills to communicate effectively with various levels of management in both business and technical communities. | 9/22/2019 |
| 13903 | Avantec Vascular Sunnyvale, CA R&D ENGINEER I BS in engineering Exp: 1-3 years medical design experience |
Responsible for providing creativity to the mechanical engineering design and development of new invasive and non-invasive medical device products. Researches, develops, designs (utilizing CAD design software), and evaluates technical suitability of mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Must be able to clearly communicate designs and all requisite requirements to support personnel both verbally and in writing. | 9/22/2019 |
| 13904 | Avedro Burlington, MA Associate Research Formulation Scientist MS or BS in pharmacology, biochemistry, or analytical chemistry Exp: 0-2 y ears |
In this role you will be responsible for assisting with the formulation development and testing efforts within our ocular drug development program. Located primarily at our labs in Burlington, MA and interfacing with other group members in our Waltham, MA offices, you will join a growing dynamic team of interdisciplinary scientists at a world leading company on the forefront of corneal crosslinking science. | 9/22/2019 |
| 13905 | Avid Bioservices Tustin, CA Associate Specialist/Specialist, Quality Assurance (GMP) BS in sciences Exp: 0-3 years |
The Quality Assurance Associate Specialist/Specialist is an individual contributor who solves a variety of issues following cGMP regulations and company standards. Assist in the release of API batches and lots. Review of Manufacturing Batch Production Records - Must have at least 6 months to 1 year or more experience. Collaborate with departments to ensure that all review activities are executed efficiently per governing SOPs. | 9/22/2019 |
| 13906 | Avion Pharmaceuticals Boston, MA Pharmaceutical Sales Representative BS/BA Exp: 1 year in business-to-business ales |
The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’s offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. | 9/22/2019 |
| 13907 | Avion Pharmaceuticals Orlando, FL Pharmaceutical Sales Representative BS/BA Exp: 1 year in business-to-business ales |
The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’s offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. | 9/22/2019 |
| 13908 | Avion Pharmaceuticals Worcester, MA Pharmaceutical Sales Representative BS/BA Exp: 1 year in business-to-business ales |
The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’s offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. | 9/22/2019 |
| 13909 | Avomeen Ann Arbor, MI ANALYTICAL CHEMIST BS/MS in chemistry or related Exp: 0-5 years |
We are looking for a talented individual to fill an Analytical Chemist position at our Ann Arbor, MI facility. Learn techniques spanning across the entire spectrum of analytical chemistry from wet chemistry to HPLC, NMR, Mass Spectrometry, FTIR, GC and GC-MS. Execute projects in support of client needs including product deformulation and product development, failure analysis and problem solving, impurity identification, extractable and leachable studies, and structural characterization | 9/22/2019 |
| 13910 | Axogen Tampa , FL Quality Systems Engineer BS in engineering or sciences Exp: 1-5 years |
The Quality Compliance Engineer will provide support in the implementation, maintenance, and improvement of company-wide quality management systems, procedures and support processes. Proactively monitors the various elements of the quality system to help ensure compliance with quality system regulations and applicable national and international quality standards. Ensures processes and tools are established to ensure ongoing compliance with applicable requirements. Supports external audits by the FDA, AATB, the Notified Body, other regulatory bodies and third parties, and coordinates responses to applicable audit findings. | 9/22/2019 |
| 13911 | Axogen Vandalia, OH Quality Engineer BS in engineering, pharma sciences, life sciences, etc. Exp: 1-3 years in quality/compliance |
The Quality Engineer will provide quality engineering and quality assurance support for Manufacturing Operations to ensure new/improved and current medical products and processes are in compliance with applicable standards and regulations. Confer with external and internal departments (example Product Development, Clinical, Marketing, Sales, and Operations) concerning product design to ensure user needs are met. Implement Quality systems and processes. The Quality Engineer will write standard operating procedures, work instructions, and other Quality documentation. | 9/22/2019 |
| 13912 | Axsome New York, NY Clinical Trials Assistant BS in biological/physical sciences Exp: 1 year in clinical department |
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. | 9/22/2019 |
| 13913 | Azzur Group Washington DC, DC Validation Engineer BS in engineering/sciences Exp: 1-7 years in regulated manufacturing |
Ideal candidates will exhibit, or have the willingness to develop, the following qualities: Strategic thinker with strong analytical skills who can translate client needs into actionable value-added projects/results. Understands the competitive landscape of the medical device, pharmaceutical, and biotechnology industry. Willing to work hands on, assist with building client libraries, learn from a mentor and become a mentor for others. | 9/22/2019 |
| 13914 | Bachem Torrance, CA Research Sales Representative BS in sciences Exp: 1-2 years in sales |
The Research Sales Representative will be responsible for selling the company’s products and services by contacting prospective and established customers. The Research Sales Representative will follow up on leads and establish close customer contacts to promote the company’s products to select accounts as designated by Sales Management. | 9/22/2019 |
| 13915 | Associates of Cape Cod Inc. Falmouth, MA LOGISTICS TECHNICIAN I HS Diploma Exp: 1-3 years in shipping/receiving |
Work as part of a team where needed in the Receiving/Shipping/Labeling and Kitting departments. Works in conjunction with departmental SOP's, maintain accurate control of inventory in the finished goods and raw material warehouses. Receives/stores all materials for ACC's use and performs all necessary receiving transactions within Data Management System. Works in Shipping in fulfilment of customers' orders and generation of associated shipping documentation. Assists in labeling of product, packaging final product for sale and general departmental coverage during absenteeism. | 9/22/2019 |
| 13916 | Associates of Cape Cod Inc. Falmouth, MA QUALITY CONTROL ANALYST I BS in relevant sciences Exp: 0-2 years lab experience |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. | 9/22/2019 |
| 13917 | Avid Bioservices Tustin, CA Biomanufacturing Associate/Sr. Associate (Upstream Cell Culture) BS/BA in biological sciencecs Exp: 1-3 years cGMP mammalian cell/fermentation work |
The Manufacturing Associate/Sr. Associate performs multiple aspects of cGMP contract cell culture manufacturing in a multi-product manufacturing facility, including, but not limited to: production, documentation, writing reports, requesting and purchasing materials, and scheduling equipment services and calibrations. The Manufacturing Associate will play an integral role in ensuring the production and on-time release of quality products. | 9/22/2019 |
| 13918 | Avid Bioservices Tustin, CA Biomanufacturing Associate/Sr. Associate (Downstream Purification) BS/BA in life sciences Exp: 1 or more year in industry |
ou get to participate in a variety of tasks including purification of biologics, keeping up-to-date GMP documentation, writing reports, ordering materials, and scheduling equipment services. You are conscientious about maintaining strict compliance with GMP manufacturing practices as you adhere to our standard operating procedures. | 9/22/2019 |
| 13919 | Applied Medical Technology Brecksville, OH Mold Process Engineer AS/AA in plastics/technology Exp: 1-4 years in plastic processing |
Develop optimum molding processes for manufacturing medical components. Provide recommendations and implement improvements to production processes, methods and controls. Provide support and leadership in the development of in the injection molding processes and tools. | 9/20/2019 |
| 13920 | Applied Medical Technology Brecksville, OH Entry Level Injection Molding Machine Operator- 1st Shift HS Diploma Exp: Entry Level |
Operates injection molding machines according to specific schedules and procedures. Prepares mold inserts and reviews molded component integrity. Remove molded components from the mold once the machine has finished its cycle. When applicable test parts during machine cycle to predetermined specifications | 9/20/2019 |
| 13921 | Applied Medical Technology Brecksville, OH Associate Sales Representative BS/BA Exp: 1-2 years sales experience |
The purpose of this position is to assist sales reps in making goal. Candidate must maintain an understanding of distribution channels and key industry leaders. Must be willing to travel as needed for tradeshows, conferences and in servicing events. Duties include training and in-servicing of customers and assisting sales reps as needed. This will involve up to 75% travel throughout the United States. | 9/20/2019 |
| 13922 | Applied Molecular Transport South San Francisco, CA Research Associate BS,MS in chemistry, biochemistry, biological sciences Exp: 1-5 years |
The successful candidate will have extensive understanding of protein chemistry, protein characterization, and analytical techniques. The position will involve regular communication and collaboration with an interdisciplinary team within AMT and with outside contractors/consultants. Perform analytical method development for LC based assays such as SEC, IEX and reversed-phase HPLC, and other protein-based analysis (i.e. SDS-PAGE, western blot, A280) | 9/20/2019 |
| 13923 | Applied Stem Cell Milpitas, CA Research Associate, Molecular Biology BS/MS in biological sciences Exp: Entry Level |
We are looking for a Research Associate, Molecular Biology to join our Life Sciences department. This is a hands-on lab-based role in the Life Sciences Service program with a focus on generating engineered cells and animal models using ASC’s gene editing technologies. | 9/20/2019 |
| 13924 | Applied Stem Cell Milpitas, CA IT Support Technician AS/AA or BS/BA in computer sciences Exp: 1 or more year in IT |
We are looking for a part-time IT Support Technician to provide prompt IT support to the daily operations of various IT systems/devices. This technician is also responsible to set up new computers and systems for new hires and to decommission them when needed. This is a non-exempt role requiring an average of 20-25 hours a week. | 9/20/2019 |
| 13925 | Applied Stem Cell Milpitas, CA Microinjectionist BS in biological/animal sciences, MS preferred Exp: 1 or more year in microinjections |
We are looking for a Microinjectionist who will be responsible for the animal model division, in conducting transgenic animal production through microinjection of DNA/RNA/protein into pronuclear stage embryos or making chimeric animals with injection of targeted ESCs into morula/blastocysts. | 9/20/2019 |
| 13926 | Evotec Princeton, NJ Research Associate - Assay BS/MS in biological sciences Exp: 1-3 years in lab experience |
The successful candidate will actively contribute to ongoing and future collaborations with multiple discovery partners in the design, development and execution of novel in vitro assays to support early stage drug discovery and development. Working with a team of scientist in the design, validation and execution of in vitro assays (both biochemical and cellular) for characterization of small and large molecule drug candidates | 9/20/2019 |
| 13927 | Evotec Watertown Cyprotex, MA Associate Scientist BS in biological sciences Exp: 1-2 years in industry |
The team is looking for a highly motivated Associate Scientist that will be responsible for routine screening of compounds in various in vitro toxicology assays. Responsible for planning and conducting high and low throughput toxicology screens, processing data to a high quality of standards, and within specified time frames. | 9/20/2019 |
| 13928 | Aquestive Warren , NJ Formulation Scientist MS in sciences/chemistry Exp: 0-5 years in pharma |
A member of the R&D team responsible for the design and development of drug products for the targeted delivery of active pharmaceutical ingredients, including thin films for transmucosal delivery. Conducts laboratory activities and formulation work in support of product development, product characterization and process optimization. Prepares laboratory prototype samples for preclinical, in-vitro and stability evaluations | 9/20/2019 |
| 13929 | Abor Biotechnologies Cambridge, MA Software Engineer - Research MS or higher in engineering/sciences Exp: 1-2 years |
At Arbor, you will be at the cutting edge of biodiscovery, systematically searching through nature’s diversity to discover and engineer new technologies for improving human health and sustainability. As a Software Engineer in Research, you will focus on building a search engine from the ground up. You will have significant latitude towards ideation, problem definition, and finding novel uses of machine learning. | 9/20/2019 |
| 13930 | Archer Boulder, CO Associate BS/BA in sciences Exp: 1-2 years in manufacturing |
Associate level position for manufacturing medical devices in accordance with controlled procedures (SOPs) in compliance with Good Manufacturing Practice (GMP) regulations and current GMP (cGMP) guidelines. Manufactures solutions, labels and fills containers, labels and assembles kits. Compiles auditable electronic or paper records of manufacturing, maintains equipment logs and monitors supplies. | 9/20/2019 |
| 13931 | Arcturus San Diego, CA Public Relations & Marketing Associate BS/BA in sciences or business Exp: Entry Level |
In this role, you will create PR/Marketing collateral, assist with website design, graphics, and plan publicity strategies and campaigns. You will be responsible for research, asset creation and organization to support corporate investor relations activities. | 9/20/2019 |
| 13932 | Arcturus San Diego, CA Research Associate, Translational Biology (In Vivo) Associates/Bachelors in sciences Exp: 1-3 years of small animal handling |
The successful candidate will bring hands-on experience performing in vivo experiments and with various animal handling techniques such as pharmaceutical agent dose administration (IV, PO, IP, IM) and blood/tissue collection. We seek candidates who are team oriented, diligent and meticulous, who display initiative and will be able to contribute intellectually to our science. | 9/20/2019 |
| 13933 | Arcturus San Diego, CA Research Associate, Translational Biology BS/BA in sciences Exp: 1-3 years of small animal handling |
The successful candidate will bring hands-on experience developing assays and performing in vivo, ex vivo experiments. Animal handling techniques such as pharmaceutical agent dose administration (IV, PO, IP, IM) and blood/tissue collection are required. We seek candidates who are team oriented, diligent and meticulous, who display initiative and will be able to contribute intellectually to our science. | 9/20/2019 |
| 13934 | Arcus Biosciences Hayward, CA Research Associate: Quantitative Biology BS/MS in biological sciences Exp: 0-3 years |
The successful candidate will have strong organizational skills and attention to detail, coupled with excellent practical laboratory skills, and aptitude and enthusiasm for automated laboratory assay techniques. Responsibilities include: Mammalian cell culture. Biological sample banking. Biology and tissue culture lab management, safety program support. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. | 9/20/2019 |
| 13935 | Arcus Biosciences Hayward, CA Research Associate BS/MS in chemistry or related Exp: 1-4 years |
The successful candidate will be responsible for conducting in-vitro ADME studies, qualitative and quantitative analysis of small molecules using LC-MS/MS, to support multiple drug discovery and development projects. Responsibilities include, but are not limited to: LC-MS/MS method development and quantitative analysis of in vitro and in vivo samples in various biological matrices. Perform in vitro ADME assays such as metabolic stability, CYP inhibition, plasma protein binding and blood to plasma partitioning; develop new assays as needed. | 9/20/2019 |
| 13936 | Arcus Biosciences Hayward, CA Research Associate BS/MS in chemistry or related Exp: 1-4 years |
The successful applicant will be responsible for performing bioanalysis of in vitro and in vivo samples to support discovery and development programs. Develop, troubleshoot, and validate LC-MS/MS based bioanalytical methods. Analyze, summarize and report preclinical pharmacokinetic and toxicokinetic results. Conduct in vitro ADME experiments such as metabolic stability, plasma protein binding, CYP inhibition and induction assay as necessary | 9/20/2019 |
| 13937 | Arcus Biosciences Hayward, CA Research Associate/Sr. Research Associate, Immunology BS in biological sciences Exp: 1-2 years in research |
The role will be responsible for executing a variety of experiments using in vivo models and in vitro assays in order to validate new targets and understand mechanism of action and pharmacodynamic properties of drug candidates. A successful candidate will contribute as part of a multidisciplinary team in a fast-paced environment to plan and execute experiments and subsequently collate, document, interpret, and present data internally. | 9/20/2019 |
| 13938 | Array Boulder, CO Research Associate / Associate Scientist - Medicinal Chemistry MS in organic chemistry Exp: 0-2 years |
Array’s medicinal chemistry group has openings for motivated synthetic organic chemists who are able to work in a team environment to deliver quality drug candidates with a sense of urgency. Responsibilities include: Demonstrates technical competency in reaction set-up, product isolation, purification and analysis, from milligram to multigram scale. Develop an understanding of SAR, contribute to analog design. Collaborate closely with colleagues to discuss data and generate new ideas | 9/20/2019 |
| 13939 | Go Beyond RNA Rockville, MD Lab assistant - Molecular Biology BS in biological sciences Exp: 1-2 years wet lab experience |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. | 9/20/2019 |
| 13940 | Arrowhead Madison, WI Animal Technician (Procedures) HS Diploma Exp: 6 months rodant research |
Arrowhead is seeking an experienced Animal Technician to join our Laboratory Animal Resources staff. This is an excellent opportunity to utilize and advance the ideal candidate’s laboratory animal skills in a progressive, state-of-the-art and diverse facility. | 9/20/2019 |
| 13941 | Arrowhead Madison, WI Associate Production Chemist HS Diploma Exp: 0-5 years |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. The successful candidate will be expected to: Follow batch records, SOPs, and work instructions to detail. Document all operations in batch records and notebooks. Comply with GMP protocols | 9/20/2019 |
| 13942 | Arrowhead Madison, WI Research Technician, Biology BS in biological sciences Exp: 0-4 years lab experience |
Arrowhead Research seeks a full time Research Technician to join its drug targeting team at its research and development facility in Madison, WI. The candidate should be highly motivated, and enjoy working with a team of scientists in a fast-paced and highly cross-disciplinary environment. The individual will be primarily responsible for providing technical assistance in RNA and DNA isolations, cell culture, and general laboratory maintenance. | 9/20/2019 |
| 13943 | Aquestive Portage, IN Coating Scientist - Temporary BS or AS in sciences Exp: 1-2 years in pharma manufacturing |
Responsible for a basic knowledge of all phases of the production operation from mixing through coating. On each shift, each Coating Scientist will be responsible for one of the following production operations: weighing, mixing, or coating, slitting, as assigned by the Production Supervisor. | 9/20/2019 |
| 13944 | Acelity South Burlington, VT Field Servive Representative I HS diploma or equivalent Exp: 1 year |
This position is responsible for providing world class customer service during the provision, return and servicing of medical equipment inclusive of responding to product inquiries or other identified customer needs. The daily responsibilities encompass the preparation of medical equipment for patient use to include sanitization and disinfection, quality control testing, preparation for use and transportation of the equipment to and from customer locations utilizing a company provided vehicle. In addition to preparation and provision of medical equipment, employees in this function are required to learn and operate within the company defined policies and procedures to maintain compliance with the regulated requirements for medical devices. Additional responsibilities include maintenance of a safe and clean service center working environment and company vehicles. etc. | 9/17/2019 |
| 13945 | Acelity Cinnaminson, NJ Field Servive Representative I HS diploma or equivalent Exp: 1 year |
This position is responsible for providing world class customer service during the provision, return and servicing of medical equipment inclusive of responding to product inquiries or other identified customer needs. The daily responsibilities encompass the preparation of medical equipment for patient use to include sanitization and disinfection, quality control testing, preparation for use and transportation of the equipment to and from customer locations utilizing a company provided vehicle. In addition to preparation and provision of medical equipment, employees in this function are required to learn and operate within the company defined policies and procedures to maintain compliance with the regulated requirements for medical devices. etc. | 9/17/2019 |
| 13946 | Acelity Arlington, TX Field Servive Representative I HS diploma or equivalent Exp: 1 year |
This position is responsible for providing world class customer service during the provision, return and servicing of medical equipment inclusive of responding to product inquiries or other identified customer needs. The daily responsibilities encompass the preparation of medical equipment for patient use to include sanitation and disinfection, quality control testing, preparation for use and transportation of the equipment to and from customer locations utilizing a company provided vehicle. In addition to preparation and provision of medical equipment, employees in this function are required to learn and operate within the company defined policies and procedures to maintain compliance with the regulated requirements for medical devices. etc. | 9/17/2019 |
| 13947 | Acella Pharmaceuticals Irvine, CA Pharmaceutical Sales Representative BA/BS Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’s offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. etc. | 9/17/2019 |
| 13948 | Advanced Bionics Valencia, CA Quality Control Inspector I HS diploma or equivalent Exp: 1-2 years |
Responsible for performing visual, mechanical and electrical inspections at subassembly and final assembly levels. DUTIES: 1. Perform visual and mechanical inspections at sub-assembly and final assembly levels, using engineering drawings/specifications and general quality control standards. 2. Records inspection data. 3. Review manufacturing documentation to ensure that all assembly, testing and inspection steps were performed in accordance to specifications. etc. | 9/17/2019 |
| 13949 | AGC Biologics Bothell, WA Development Associate I (Contract, Temp-to-Perm) Monday-Friday HS diploma/AA in life sciences or engineering Exp: 0-3 years |
This is a Development Technician position in the Process Development Support group. Primary responsibility will be to support the process development team processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for lab support. Under general supervision, this person carries out routine to moderately complex lab operations. Responsibilities: Lab maintenance including cleaning, autoclaving parts, stocking laboratory supplies and performing maintenance on laboratory equipment. etc. | 9/17/2019 |
| 13950 | AGC Biologics Bothell, WA Development Associate I (Contract, Temp-to-Perm) Sun-Wed AA/BS in life science or engineering Exp: 0-3 years |
This is a Development Associates position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. etc. | 9/17/2019 |
| 13951 | AGC Biologics Bothell, WA Development Associate I-II AA/BS in life science or engineering Exp: 0-2 years |
This is a Development Associate I position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. etc. | 9/17/2019 |
| 13952 | AGC Biologics Bothell, WA Downstream Manufacturing Associate HS diploma to BA/BS Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. etc. | 9/17/2019 |
| 13953 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I-IV BS in chemistry, biology, or related Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. etc. | 9/17/2019 |
| 13954 | AGC Biologics Bothell, WA Manufacturing Associate III - Upstream BS in chemistry, biology, or related Exp: 1-4 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Executes bioprocess operations successfully primarily in Cell Culture/Upstream manufacturing. CIP/SIP/PT operations: cleaning, assembly, sterilization, disassembly, pressure test and operation of primary process equipment. Unit operations described in standard operating procedures and batch records (50%-100% of effort). Recommends and executes projects and changes to bioprocess operations to reduce risk and increase efficiency. etc. | 9/17/2019 |
| 13955 | AGC Biologics Bothell, WA Manufacturing Support Technician HS diploma or equivalent Exp: 0-6 years |
We are seeking an experienced and highly motivated Manufacturing Support Technician to join our expanding Manufacturing team. PRINCIPAL RESPONSIBILITIES: Support product process unit operations described in standard operating procedures and batch records (100% of effort). Anticipates and minimizes deviations from support procedures. Stocking of supplies and gowning materials in GMP clean room areas. Weigh and dispensing of chemicals and processing materials. etc. | 9/17/2019 |
| 13956 | AGTC Alachua, FL QA Specialist I BS in a scientific discipline Exp: No experience |
Essential Duties and Responsibilities: Support the development, implementation, and improvement of corporate quality systems that support early, mid and late phase gene therapy clinical programs. Increase compliance awareness and promote a culture of quality throughout the company, with a focus on laboratory and manufacturing operations. Collaborate with multiple functions to perform QA oversight and ensure quality-related activities are executed efficiently. Write, review and revise standard operating procedures. etc. | 9/17/2019 |
| 13957 | AGTC Alachua, FL Pre-Clinical R&D Research Associate I - Cloning & Production MS in a biologcal science Exp: No experience |
Essential Duties and Responsibilities: Plasmid construction and large-scale plasmid DNA production. AAV vector production, purification and characterization. Design and develop new assays with minimal supervision. Maintain relevant laboratory supplies and equipment as needed. Draft SOPs, tech report and study reports. etc. | 9/17/2019 |
| 13958 | AKESOgen Peachtree Corners, GA Research Associate BS/MS in a clincal, health, or life sciences field Exp: 1+ years |
This individual is a Research Associate who will work with a team of research associates and scientist at AKESOgen. The Research Associate will work under the general direction of a Team Lead. This individual will perform extractions on a variety of sample types, genotyping on Affymetrix and/or Illumina platform equipment maintenance, solution and reagent preparation in addition to other tasks in laboratory. All duties are subject to change by managers during employment. etc. | 9/17/2019 |
| 13959 | Akorn Vernon Hills, IL Formulation Scientist II BS/MS in pharmaceutical sciences or related Exp: 0-4 years |
We seek talented Formulation Scientists at various levels to join our expanding R&D team who will be responsible for developing the final product formulation, process procedures and packaging of semisolids, suspensions and solutions, lotions, nasal sprays, inhalations, sterile injectable and ophthalmic products etc. Literature searching and review, patent searching and interpretation, performing risk assessment for formulation/process development, conducting experimental design and execution of lab scale, pilot scale developmental batches to support the final formulation and processes. Evaluation and selection of active, inactive raw materials and packaging components for various products. etc. | 9/17/2019 |
| 13960 | Akorn Cranbury, NJ Analytical Scientist I BS in chemical or life sciences Exp: 0-4 years |
We seek talented Analytical Scientists at various levels to join our expanding R&D team. You will be responsible for methods and process development for ANDA topical, suspensions and solutions, nasal sprays, inhalations, sterile injectable and ophthalmic products. You will develop and validate new analytical methods, conduct stability studies and perform sample testing to support regulatory submissions. ESSENTIAL FUNCTIONS: Independently develop analytical methods for drug substances, drug product, preservatives and degradation/impurities in the new drug products. etc. | 9/17/2019 |
| 13961 | Acumed Boston, MA Sales Associate - New England BA/BS Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 9/17/2019 |
| 13962 | Acumed unspecified, KY Sales Associate - Kentucky BA/BS Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 9/17/2019 |
| 13963 | Acumed Scranton, PA Sales Associate - Danville/Scranton, PA BA/BS Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 9/17/2019 |
| 13964 | Acumed Hillsboro, OR Machinist 2 (Day Shift) HS diploma or equivalent Exp: 1-2 years |
The Machinist sets up and operates a variety of machine tools to produce precision parts and instruments. The Machinist is responsible for ensuring product is loaded and unloaded correctly per standard operating procedures. etc. | 9/17/2019 |
| 13965 | Acumed New York, NY Sales Associate - NYC BA/BS Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 9/17/2019 |
| 13966 | Acumed Kansas City, MO Sales Associate - Kansas City, MO BA/BS Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 9/17/2019 |
| 13967 | Ani Pharmaceuticals Baudette, MN Distribution Worker I HS Diploma/GED Exp: Entry Level |
These responsibilities include order fulfilment, receiving, stocking of materials, replenishments, cycle counting, and returned goods within the inventory control area. Performs packing, labelling, checking and confirming in the Shipping area. Works with the parcel shipping and Bill of Lading systems. Operates an electric pallet jack, and forklift operation for loading/unloading trucks. | 9/15/2019 |
| 13968 | Ani Pharmaceuticals Baudette, MN Operator I - Production (1st, 2nd and 3rd Shift) HS Diploma/GED Exp: 1-2 years |
Assists in material handling, equipment set-up and breakdowns, documents process according to Master Production Records, and works with trained operators at assigned work centers to learn all aspects of the position, including batch record documentation, equipment set-up, operation and clean up. | 9/15/2019 |
| 13969 | Ani Pharmaceuticals Baudette, MN QC Chemist/Sr. QC Chemist BS/BA in chemistry, microbiology, or related Exp: 1-3 years minimum |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 9/15/2019 |
| 13970 | Ani Pharmaceuticals Baudette, MN Contracts Support Associate AS/AA Exp: 1-2 years related experience |
This position works within the Finance Department is responsible for daily data entry as it relates to Contract Support related activities. This includes order processing, shipping paperwork, invoicing, advanced ship notices, product returns and other duties as assigned. | 9/15/2019 |
| 13971 | Antech Middletown, CT Laboratory Generalist BS in medical technology or related Exp: 0-1 years |
As a Laboratory Generalist I you will work with the Lead Laboratory Technician to ensure the lab is running efficiently to meet and/or exceed goals. The ideal candidate will have prior experience performing some clinical diagnostic testing. Must have experience in at least three clinical areas including Hematology, Chemistry, Processing, etc. Perform all required quality control per QA guidelines. Train on all areas to include Processing, Chemistry, Hematology, UA and Coag according to all SOP’s. | 9/15/2019 |
| 13972 | Antech Fountain Valley, CA Histology Aide HS Diploma/GED Exp: 0-2 years |
Antech Diagnostics is looking for outstanding Laboratory Aides and Assistants for shift positions throughout our veterinary diagnostic reference lab locations. The ideal candidates will have experience working in either a reference or hospital laboratory, or have strong experience performing lab duties as a Vet Tech. The Laboratory Aide is responsible for setting up instruments, collection of samples, load samples into instruments and prepare samples for laboratory technicians. | 9/15/2019 |
| 13973 | Antech Fountain Valley, CA QA Specialist BS in medical technology or related Exp: 1 year in clinical lab |
Our QA Specialists are responsible for ensuring consistent quality of diagnostic testing, assist with validation of methods/assays, perform QA surveys and maintain good documentation and excellent lab/business practices. You will be responsible for all quality assurance and quality control functions relating to diagnostics testing, lab safety, analytical and instrumentation. You will ensure consistent quality of diagnostics testing, assist with validation of methods/assays, perform QA surveys and maintain good documentation and excellent lab/business practices. | 9/15/2019 |
| 13974 | Antech Fountain Valley, CA Float Laboratory Technician BS in medical technology or related Exp: 1 year in clinical lab |
Antech Diagnostics, the largest exclusively commercial veterinary diagnostic laboratory in the nation, is in search of a Float Laboratory Technician working out of our Lake Success, New York laboratory and reporting directly to the Lab Manager. The Ideal Candidate will have prior experience as a Medical Technician that involved performing some clinical diagnostic testing & using testing equipment. In this integral role you will perform tests in all areas of the laboratory such as: Chemistry, Hematology, Coagulation, Urinalysis, Serology, Parasitology, Histology. | 9/15/2019 |
| 13975 | Applied Meidcal Rancho Santa Margarita, CA Production Associate (Assembler/Machine Operator) HS Diploma/GED Exp: 1-2 years work experience |
As a Production Associate, you will be responsible for working within the framework of a team in a cleanroom or manufacturing environment, and performing the following activities: Perform all manufacturing operations in a cleanroom or non-cleanroom environment such as assembly, inspection, and machine operations. Comply with Applied Medical Quality Systems (QS) including SOPs, MIs, QIs and TMs. Perform manufacturing operations efficiently with or without tools and/or equipment | 9/15/2019 |
| 13976 | Applied Meidcal Rancho Santa Margarita, CA Quality Engineer I,II HS Diploma/GED Exp: 1 year in medical devices |
As a Specialist I/II or Engineer I/II on the Regulatory Affairs(RA)/Quality Systems(QS) Team, you will be responsible for working within the framework of a team and performing the following activities: Monitor and ensure conformance through the understanding of standards and regulations. Manage projects to maintain and improve the quality system by establishing or updating procedures. Participate in internal and external audits | 9/15/2019 |
| 13977 | Applied Meidcal Rancho Santa Margarita, CA Project Engineer - Construction BS/BA in construction management, engineering or related Exp: 0-3 years |
As a Project Engineer, you will be responsible for working within the framework of a team and performing the following activities: Update construction schedules based on team input. Receive, review, forward and track status of submittals. Initiate, prepare, review, track, and distribute RFIs. Assist in management of project permit process | 9/15/2019 |
| 13978 | Applied Meidcal Lake Forest, CA Mold Maintenance Technician HS Diploma/GED Exp: 1 year of mold maintenance |
As a Mold Maintenance Technician, you will be responsible for working within the framework of a team and performing the following activities: Maintain thermoplastic molds to ensure consistent quality, output and yield. Perform preventive maintenance on injection mold tooling. Communicate effectively with production team members, Team Leaders engineers, and inspectors to ensure quality installation of molds | 9/15/2019 |
| 13979 | Allergan Austin, TX Accounts Receivable Administrator I BS in finance or accounting Exp: 1-2 years in related |
Responsible for analyzing and collecting past dues for specified accounts. Negotiates with customers without jeopardizing their relationship with Allergan to collect all past due invoices. Has knowledge of commonly used concepts, practices, and procedures within a particular field. Relies on experience and judgment to plan and accomplish tasks. Performs a variety of complicated tasks to minimize financial losses and obtain best possible DSO. Daily activities include establishing objectives, identifying areas of improvement internally and externally. | 9/14/2019 |
| 13980 | Allergan Livonia, MI Clinical Sales Representative BS/BA Exp: 1 year in business to business sales |
As a pharmaceutical Sales Representative, you will have the opportunity to regularly call on health care professionals (primary care physicians, clinics, hospitals and pharmacies) within a specific geographic area. Day-to-day responsibilities consist of supporting the promotional efforts behind Allergan products, which includes organizing, tracking and distributing FDA regulated sample products to health care professionals. | 9/14/2019 |
| 13981 | Allergan Mentor, OH Clinical Sales Representative BS/BA Exp: 1 year in business to business sales |
As a pharmaceutical Sales Representative, you will have the opportunity to regularly call on health care professionals (primary care physicians, clinics, hospitals and pharmacies) within a specific geographic area. Day-to-day responsibilities consist of supporting the promotional efforts behind Allergan products, which includes organizing, tracking and distributing FDA regulated sample products to health care professionals. | 9/14/2019 |
| 13982 | Alliance Spine San Antonio, TX Medical Sales Representative BS/BA Exp: 1 year operating room experience |
Responsible for working at the direction of the Chief Operating Officer and/or Managing Partner to help support the sales functions within the defined geography. Medical Sales Representative will assist in retaining and penetrating existing customers (surgeons and distributors) and finding new business. The Medical Sales Representative is responsible for field-based customer service, case coverage as necessary, and sales prospecting as assigned by the Chief Operating Officer and/or Managing Partner, generating new business, sales logistics, product knowledge, product training, and maintaining inventory assets. | 9/14/2019 |
| 13983 | Amarex Bethesda, MD IT HELP DESK TECHNICIAN LEVEL 1 BS/BA Exp: 1 year related experience |
The IT Help Desk Technician Level 1 is responsible for end user support, upgrades, customization, and system integration. First point of contact for troubleshooting of IT problems; resolving the problem if possible, with an appropriate sense of urgency. Provide IT support to end users, both on- and off-site. | 9/14/2019 |
| 13984 | Amarex Bethesda, MD CLINICAL DATA COORDINATOR (two openings) BS/BA Exp: 1 year related experience |
The Clinical Data Coordinator is responsible for timely validation of clinical trial data. Review case report forms and clinical data sets for errors, discrepancies and protocol violations. Organize and maintain clinical study databases to support regulatory submissions. Communicate orally and/or written, in a timely and effective manner, with the appropriate internal or external individuals involved in the project | 9/14/2019 |
| 13985 | Amarex Bethesda, MD PROGRAMMER ANALYST I BS/BA in computer sciences or related Exp: 1 year related experience |
The Programmer Analyst I is a computer programming position responsible for delivering technical services relating to clinical trials data. This includes working with Electronic Data Capture (EDC) and other data management applications to achieve project integrity and the delivery of on-time, quality data. The Programmer Analyst I analyzes the feasibility of program requirements to develop applications that meet FDA guidelines. | 9/14/2019 |
| 13986 | Ambry Genetics Aliso Viejo, CA Quality Assurance Engineer BS/BA in computer sciences or related Exp: 0-2 years in software quality |
You will be working in a team that is handling one or two applications. You will be getting requirements from a QA manager and will be with the QA development team. You are responsible for the documentation, development and execution of basic manual test cases. You will also be working with the application development team for creating data sets for testing, debugging issues, and improving products. Your end users are mostly internal and need to be able to support them when necessary. | 9/14/2019 |
| 13987 | Ambry Genetics Aliso Viejo, CA Research Associate II, Assay Development - R&D MS in life sciences Exp: 1-2 years lab research |
Research Associate II is responsible for assisting senior R&D staffs with minimal supervision to design, develop, and validate clinical diagnostic assays spanning a wide range of Next-Generation sequencing and microarray technologies. | 9/14/2019 |
| 13988 | Ambry Genetics Aliso Viejo, CA Research Associate I BS or MS in life sciences Exp: 0-2 years lab experience |
Research Associate I is responsible for assisting senior R&D staffs to design, develop, and validate clinical diagnostic assays spanning a wide range of Next-Generation sequencing and microarray technologies. Aid in the design and development of clinical diagnostic assays for use in a CLIA/CAP regulated setting. Perform research experiments, such as primer design and preparation, PCR, electrophoresis, gel imaging and analysis, | 9/14/2019 |
| 13989 | Ambry Genetics Aliso Viejo, CA Software Engineer, Bioinformatics MS in computational biology or related Exp: 1+ year in software development |
As a software engineer at Ambry you’ll gain industry-leading experience in AGILE software development while working at the cutting edge of clinical genetics. At Ambry, you’ll have the opportunity to develop innovative solutions and leverage the latest technologies to make our diagnostics-testing even better. The technologies we use include Perl, Python, Dancer2, MySQL, MongoDB, and Elastic Search. Knowledge of the genetics and/or genetic testing industry a huge plus and a sense of humor is a must. | 9/14/2019 |
| 13990 | Ambu Noblesville, IN Process Technician - 2nd Shift AS/AA Exp: 1 year experience |
Monitor various line and equipment functions utilizing various computer interfaces and visual observation. Perform change over, teardown, and set-up tasks. Perform, monitor, and document wastewater and lift station properties. Complete documentation to ensure compliance with relevant standards (i.e. Medical Device Directive (MDD), QSR, CMDR, ISO 13485, JPAL, production and corporate standards) | 9/14/2019 |
| 13991 | Ambu Noblesville, IN Quality Assurance Inspector - 2nd Shift HS Diploma/GED Exp: 1-3 months |
Monitor compliance to in-house standard operating procedures (SOP's) and Current Good Manufacturing Practices (CGMP's), pertaining to the manufacturing, packaging, storage, and distribution of finished product. | 9/14/2019 |
| 13992 | Amgen Tampa, FL Associate Data Engineer BS/BA Exp: 0-4 years |
The Associate will work with some of the brightest minds in the industry and get opportunities to solve some of the most challenging business problems. Amgen is using Enterprise Data Lake, cloud technology, and continuous deployment pipelines to produce science based insights to build new drug therapies for patients that address grievous illnesses. | 9/14/2019 |
| 13993 | Amgen Thousand Oaks, CA Automation Engineer MS Exp: 0-2 years in engineering |
The Automation Engineer reports to the Manager of the Automation group. The position is responsible for providing Automation Engineering support at the Amgen Thousand Oaks site. Provide system administration and ownership support for DeltaV and Utility systems. Work closely with multiple disciplines including: OIS network and site platform leads to support, plan and execute system roadmaps and as well as influence future improvements. Ensure optimal performance and reliability for process systems and equipment. | 9/14/2019 |
| 13994 | Amgen Tampa, FL Data Engineer MS in information systems Exp: 0-2 years |
In this role, you will work with some of the brightest minds in the industry, and you'll get an opportunity to solve some of the most challenging business problems. Amgen is using Enterprise Data Lake, cloud technology, and continuous deployment pipelines to produce science based insights to build new drug therapies for patients that address grievous illnesses. Applying specialized knowledge and understanding of principles, concepts and standards to moderately complex assignments | 9/14/2019 |
| 13995 | Amgen Thousand Oaks, CA Associate Manufacturing BS/BA Exp: 0-4 years in manufacturing or operations |
he Associate of Manufacturing will work in a dynamic production environment at the Amgen Thousand Oaks Drug Substance plant supporting development, clinical, and commercial launch activities. Under general supervision, employee will perform operations in the Manufacturing area, specifically B23 processes. Operations will be performed according to Standard Operating Procedures (SOPs). | 9/14/2019 |
| 13996 | Amgen Tampa, FL Associate Software Engineer - Regulatory Information Management BS/BA Exp: 0-4 years in information sciences |
Amgen is seeking an integration engineer with experience and interest in building scalable integrations for enterprise applications. The integration engineer will have a real passion for developing and maintaining robust integration for On-Prem and Cloud applications to support critical business functions. | 9/14/2019 |
| 13997 | Amgen Tampa, FL IS Engineer - Data Analytics (Business Intelligence) MS in computer sciences/maths Exp: 0-2 years in information sciences |
We are seeking an IS Engineer – Data Analytics in our Amgen Capability Center (ACC) Tampa, FL to join our Patient Safety IS team. The ideal candidate must be passionate about providing solutions for advanced analytics and data processing. You will collaborate with our Patient Safety business and product teams to define and build the reporting and data visualization solutions enabling faster and better-informed decision-making | 9/14/2019 |
| 13998 | Amgen Juncos, PR Associate Mfg - AML 14 BS/BA in life sciences/engineering Exp: 0-2 years |
The Associate Manufacturing role will support the Drug Product Filling operations according to Standard Operating Procedures (SOPs). Will perform and monitor critical processes, execute routine protocols, and regularly draft and revise documents such as Manufacturing Procedures and SOPs. Perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams. Employee may also have the responsibility of owning NC/CAPA’s. May identify, recommend, and implement improvements related to routine functions in a Non-Standard Shift environment. Several positions available. | 9/14/2019 |
| 13999 | Amicus Theraputics Philadelphia, PA Associate Scientist, Clinical Assay and Reagent Development MS in sciences Exp: 0-2 years |
The successful candidate will support the development and execution of in vitro and analytical biomarker assays to drive our discovery programs and provide critical support for clinical Gene Therapy programs in neurological lysosomal storage disorders. Support development of specific reagents for the characterization of lysosomal glycoproteins. Protein purification from mammalian cell lines. etc | 9/14/2019 |
| 14000 | Amneal Pharma East Hanover, NJ QA Inspector I HS Diploma/GED Exp: 1 year in QA |
The QA Inspector I monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector I must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run. | 9/14/2019 |
| 14001 | Amneal Pharma Branchburg, NJ QA Inspector I HS Diploma/GED Exp: 1 year in QA |
The QA Inspector I monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector I must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run. | 9/14/2019 |
| 14002 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - R&D Lab AS/AA or BS/BA in chemistry Exp: 0-2 years |
R&D Lab Tech performs general laboratory tasks under immediate supervision. The work involves preparation of chemical reagents/mobile phase, assistance with chemical tracking/disposal, and assistance with sample retrieval, preparation and storage. The position requires a high school diploma and some college coursework in chemistry or a related field is desired. The position also requires ability to use a personal computer, including familiarity with word processing, spreadsheet, email and database applications. | 9/14/2019 |
| 14003 | ARL Bio Pharma Oklahoma City, OK Research & Development Scientist I BS/BA in chemistry Exp: 1-2 years |
The position requires the performance of variety of task including development and validation of analytical methods and qualitatively/quantitatively testing routine and non-routine client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation (HPLC/IC) used in a chemistry laboratory. Research Scientist I work with direct supervision and reports to the lab supervisor. The Research Scientist I must be able to think and work independently, yet share ideas and work toward team goals. | 9/14/2019 |
| 14004 | ARL Bio Pharma Oklahoma City, OK Chemist I-Analytical BS/BA in chemistry or related Exp: 1-2 years |
Under general supervision, the Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 9/14/2019 |
| 14005 | AlloSource Centennial, CO Distribution & Inventory Associate HS Diploma/GED Exp: 6 months in inventory |
The role of the Distribution Inventory Associate is to facilitate proper inventory controls, stocking, and maintenance. The Inventory Associate plays an essential role in supporting the Distribution management information system, our satellite field offices, contract customers, and internal and external customers. This employee must work closely with the Distribution Supervisor as well as Department Manager/Director to assess and maintain consistent inventory levels. | 9/14/2019 |
| 14006 | Albany Molecular Research Alburquerque, NM Microbiologist II BS in life sciences Exp: 0-2 years lab experience |
Prepare, collect, and test plant purified water, manufacturing raw materials, product in-process, and finished product, and perform environmental monitoring. With limited supervision, learn and perform critical laboratory techniques and complete original work. Author problem reports and participate in investigations. This description is inclusive of EM and testing duties: actual percentages of time spent on each duty may vary based on business needs. | 9/14/2019 |
| 14007 | Allogene Therapeutics South San Francisco, CA Data Scientist BS in statistics, math, data science, engineering Exp: 1 year in manufacturing |
Provide excellence in statistical support and data analysis to drive the application of advanced and state-of-the-art statistical principles, tools and methodologies to improve process understanding, quality and compliance of the products, efficiency and capability of the processes and profitability of the organization. With general guidance provide direct technical support to Quality, Manufacturing, Development and Regulatory Affairs with hands-on analysis of process and product data. Applies appropriate statistical methods in order to improve and maintain optimal process control and product compliance. | 9/14/2019 |
| 14008 | Alamo Baltimore, MD Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in business to business sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 9/12/2019 |
| 14009 | Alamo Los Angeles, CA Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in business to business sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 9/12/2019 |
| 14010 | Alamo Austin, TX Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in business to business sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 9/12/2019 |
| 14011 | Alcami Charleston, SC Process Engineer BS/BA in engineering, pharma, chemistry Exp: 0-2 years in technical support |
The Process Engineer I (Sterile) for our parenteral site in Charleston, SC is accountable for driving results in a fast-paced environment by providing technical support for the manufacturing facility, including, troubleshooting validated processes, process deviations and investigations, transfers of new processes and technologies into the site and preparation of documentation to support validation and process transfer activities. | 9/12/2019 |
| 14012 | Alcami St. Louis, MO Microbiology Analyst BS/BA in biology/microbiology Exp: 1-5 years |
The Microbiology Analyst is accountable for driving results in a fast-paced environment by accurately and efficiently performing sample analysis, monitoring microbial cultures and identifying microbiological contaminants and pathogens using a variety of identification methods. | 9/12/2019 |
| 14013 | Alcami Charleston, SC Material Control Tech I HS Diploma/GED Exp: 1-2 years in general warehouse |
The Materials Control Technician I is accountable for results in a fast-paced environment by following applicable SOPs and cGMPs to perform tasks for the receipt, storage, inventory and distribution of raw materials, intermediate or finished drugs or drug products and components. The Materials Control Technician I uses the electronic inventory system to track, document and control all inventory. | 9/12/2019 |
| 14014 | Alcami Charleston, SC Manufacturing Tech I HS Diploma/GED Exp: 0-1 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). | 9/12/2019 |
| 14015 | Alcon Sinking Spring, PA Quality Engineer I BS/BA Exp: 0-2 years related experience |
Quality Engineering Complaint management and provide complaint trending analyses to support improvement of products manufactured in the facility. Maintain knowledge of product quality controls and failure modes. Evaluate complaint samples. Initiate and perform investigations, maintain & follow up on Quality Corrective Action Plans. Provide Progress Reports and trending to show product quality levels and respond to regulatory requests. | 9/12/2019 |
| 14016 | Alcon Sinking Spring, PA Engineer I BS/BA Exp: 0-2 years |
Assist engineering in identifying opportunities for change and realizing successful change in existing operations to attain quality, cost, and production requirements. Demonstrate knowledge of all equipment and processes in the areas of responsibility. Effectively and efficiently assist/lead efforts in product/process design. Coordinate detailed design efforts on process/equipment modifications and product changes. | 9/12/2019 |
| 14017 | Alcon Huntington, WV Engineer I, Manufacturing BS/BA in engineering, pharma, chemistry Exp: 0-2 years |
Develop, maintain, improve, and qualify molding and inspection processes for use in the manufacture and inspection of IOLs. Manage molding capacity and efficiency through process improvements and the fabrication, purchase, and qualification of new equipment. Lead technical personnel to maintain, troubleshoot, and repair molding equipment. | 9/12/2019 |
| 14018 | Aldevron Fargo, ND Laboratory Technician II HS Diploma/GED Exp: 1-2 years |
Our Laboratory Technicians play a critical role in our manufacturing process by managing the room changeover process or the solution preparation process. Detailed, thorough cleaning, line clearance, and segregation of GMP and GMP Source production areas and associated equipment while wearing appropriate gowning. Diagnostic Kit Production: assisting in vial weighing, capping, and labeling of vials as well as associated paperwork | 9/12/2019 |
| 14019 | Aldevron Fargo, ND Quality Systems Specialist I HS Diploma/GED Exp: 1+ years review compliance data or related |
We are currently seeking a Quality Systems Specialist I to join our team! The QS Specialist I will be responsible for reviewing data for compliance with systems within the quality department at Aldevron. These systems include but not limited to supplier management and electronic Quality Management Systesm (eQMS). | 9/12/2019 |
| 14020 | Aldevron Fargo, ND Metrology Technician HS Diploma/GED Exp: 1-3 years calibration/technical experience |
We are seeking a Metrology Technician! The Metrology Technician performs routine calibration, maintenance, troubleshooting, and repair of a variety of laboratory and manufacturing equipment in a cGMP environment. This individual will have the ability to perform a variety of routine and non-routine technical tasks and tests while having a great deal of initiative and judgement. | 9/12/2019 |
| 14021 | Abbott Pomona, CA QA Specialist I HS Diploma/GED Exp: 1-3 years in QA |
We have an exciting opportunity for a QA I within our Immunalysis group located at Pomona,CA In this role, you will be responsible for carrying out the daily operations in the batch record department. Demonstrated ability to carry out assignments in a timely, accurate manner and accomplishing tasks as required with little or no supervision. Work with groups within the organization to get corrections and clarifications to Device History Records. Demonstrates commitment to the development, implementation and effectiveness of Company Quality Management System per ISO, FDA, and other regulatory agencies. | 9/12/2019 |
| 14022 | Abbott San Diego, CA Lab Tech I (Second Shift) HS Diploma/GED Exp: 0-2 years |
We have an exciting opportunity for a Lab Tech I within our Abbott Rapid Diagnostics business located at San Diego, CA. In this role, you will be responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established QSR’s ISO, ISO 13485, CMDR, and other pertaining regulations under the direction of senior staff. | 9/12/2019 |
| 14023 | Alkermes Wilmington, OH QC Analyst I BS in chemistry Exp: 0-2 years |
The position requires the individual to perform routine/non-routine physical, chemical, and in-vitro assays of clinical, commercial, process and cleaning validation samples, and process development samples to support Manufacturing. Performs physical and/or chemical analyses of product to ensure stability. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. | 9/12/2019 |
| 14024 | Alkermes Wilmington, OH QA Associate I BS/BA in sciences Exp: 1-2 years in QA |
The Quality Assurance Associate will be responsible for performing functions including daily on the floor activities related to sterile manufacturing operations, on the floor batch record review, executed validation review, discrepancy identification, logbook review, AQL inspection of finished product, SAP transactions, room/utility walkthroughs, shutdown/incident form assessment/review and reconciliation, initiation of hold forms, training program support, and product shipping in a facility that manufactures sterile products in a GMP environment. | 9/12/2019 |
| 14025 | Alkermes Waltham, MA Process Development Associate BS in engineering Exp: 0-3 years |
The process development engineer will provide technical support in the development, scale-up and optimization of pharmaceutical process at various phases ranging from R&D to Commercial manufacturing. Specific areas of focus include material processability characterization, 1st and 2nd principle modeling knowledge. The role is expected to have a strong lab presence with the ability to design and execute experiments, interpret the data to improve process understanding. To be successful candidate in this role the candidate needs a good understanding in material characterization and statistical modeling is required | 9/12/2019 |
| 14026 | Alkahest San Carlos, CA Research Associate - Proteomics BS/BA in chemistry, biology or related Exp: 0-2 years lab experience |
The role will primarily support sample preparation for proteomic analysis by state-of-the-art technologies including mass spectrometry and immunoassays. Studies performed will involve cutting edge science and require innovative concepts and strategies. | 9/12/2019 |
| 14027 | 3T Biosciences Menlo Park, CA Associate Computational Biologist BS/MS Exp: 1-2 years |
TYPICAL RESPONSIBILITIES: Processing next-generation sequencing data, such as RNA sequencing. Developing and applying algorithms such as clustering, principal component analysis and others to biological data such as gene expression information and immune repertoire data. Working with Amazon Web Services to process data. Querying and organizing an SQL database. Working with a team of consultants, data scientists, and computational biologists. | 9/10/2019 |
| 14028 | 4D Molecular Therapeutics Emeryville, CA Upstream Cell Culture Manufacturing Associate BS in bioprocessing, chemical engineering, biochemistry or related Exp: 1-3 years |
Reporting to the Upstream Supervisor, you will execute cell culture and/or solution prep unit operations in cGMP clinical pilot manufacturing plant operation. You will participate in quality, compliance and safety programs for the daily manufacturing operations of biologic products to support gene therapy clinical trial and product development. In addition, you will participate in the implementation of process improvements/scale-up. Shift/weekend work and lifting 40 lbs. unassisted is required at times. | 9/10/2019 |
| 14029 | 4D Molecular Therapeutics Emeryville, CA Research Associate (Analytical Sciences & Bioinformatics) BS in life sciences Exp: 0-3 years |
Responsibilities: Follow proper safety precautions and laboratory technique in the use of chemical compounds and reagents. Perform established analytical methods such as PCR (qPCR/ddPCR), Electrophoresis, and ELISA. Design, execute and report qualification assays under the supervision of senior group members. Write and revise documents such as SOPs and technical reports. Analyze data, identify trends and troubleshoot assays. etc. | 9/10/2019 |
| 14030 | 4D Molecular Therapeutics Emeryville, CA Research Associate I/II (Upstream Process Development) BS/MS in bioengineering, biochemistry, biology or related Exp: BS: 1-3 years, MS: 0-2 years |
Major Responsibilities: Design and execute production studies leveraging 4DMT’s vector platform processes. Collaborate with process & analytical teams to screen and evaluate drug candidates across a range of indications. Draft and update batch records, electronic lab notebooks (ELN), standard operating procedures and technical reports. Responsible for documentation that is IND-supporting and will be communicated to relevant internal/external stakeholder &/or regulatory parties. Document, consolidate, interpret and communicate scientific findings with internal/external teams. Contribute to a culture that embraces continuous learning, improvement and innovation. Can work with others to expand their technical skill base and deepen their gene therapy expertise. etc. | 9/10/2019 |
| 14031 | Abbott Plymouth, MN Operator I HS diploma or equivalent Exp: 6 months |
We are seeking an experienced, high caliber Operator I. This position is responsible for the production of high quality medical devices within a manufacturing cell. | 9/10/2019 |
| 14032 | Abbott Minnetonka, MN Operator I (2nd shift) HS diploma or equivalent Exp: 6 months |
We are seeking an experienced, high caliber Operator I. This position is responsible for the production of high quality medical devices within a manufacturing cell. | 9/10/2019 |
| 14033 | Abbott Minnetonka, MN Operator I HS diploma or equivalent Exp: 6 months |
We are seeking an experienced, high caliber Operator I. This position is responsible for the production of high quality medical devices within a manufacturing cell. | 9/10/2019 |
| 14034 | AbbVie Worcester, MA Associate Scientist II/ Scientist I, Drug Product Development (Physicochemical Characterization) MS in pharmaceutics, chemistry, or related Exp: 0+ years |
The Drug Product Development team at the AbbVie Bioresearch Center in Worcester, MA is responsible for designing and developing formulations that enable delivery of AbbVie’s candidate molecules in a dosage form suitable for preclinical or clinical studies. We are seeking a highly motivated, collaborative scientist with a proven track record in physicochemical characterization of small molecule candidates and application of drug delivery approaches in preclinical development. etc. | 9/10/2019 |
| 14035 | AbbVie Lake County, IL Associate Scientist II/Scientist I, Chemistry MS in chemistry Exp: 0+ years |
AbbVie is looking for an Associate Scientist/Scientist, Chemistry with strong synthetic skills. This individual will work under the mentorship of a supervisor discovering, developing and executing routes to compounds to treat a variety of diseases. The candidate will be a member of an integrated Process Research & Development project team consisting of synthetic, structural, and analytical chemists and engineers whose goal is to identify and develop novel practical routes to newly discovered therapeutic targets. The ideal candidate will be enthusiastic and productive, with excellent communication skills and strong functional expertise in synthetic organic chemistry and compound synthesis and characterization. | 9/10/2019 |
| 14036 | Abcam Burlingame, CA Research Associate - IVD BS in biological science Exp: 1-2 years |
Based in our Burlingame Office, this manufacturing position is a great opportunity to transition into the medical device Industry! This role will be responsible for carrying out GMP manufacturing of IVD IHC primary antibodies according to the requirements of SOP’s, batch production records, and approved protocols. etc. | 9/10/2019 |
| 14037 | Abcam Cambridge, MA Sr. Research Associate BS/MS in biology or related Exp: 1+ years |
We are seeking a dynamic Service Lab Senior Research Associate to work in our Cambridge, MA office to provide customers with quality data and analyses related to our high-throughput, multiplexed immunoassays and miRNA assays. The successful candidate will participate in every aspect of the Service Lab, from experimental design through running the assays, data analysis, report generation and supporting the customers as they interpret the results. etc. | 9/10/2019 |
| 14038 | ABEC Springfield, MO Mechanical Designer AS in CAD, drafting, or equivalent Exp: 1 year |
The Mechanical Designer works under the direction of the Design Team Leader and also utilize independent judgment to perform the day-to-day project duties of designing, developing and releasing deliverables. This includes detail & assembly drawings and related bills-of material used in the fabrication of equipment for pilot and commercial scale biopharmaceutical manufacturing (largely pressure vessel assemblies for fluid & gas handling and motorized agitation systems). Primary responsibility involves generating design plans utilizing Autodesk Inventor and AutoCAD software. etc. | 9/10/2019 |
| 14039 | Abiomed Danvers, MA Software Engineer MS in computer science, math, engineering or related Exp: 1-5 years |
We are currently hiring for a Software Engineer who has experience in digital signal processing and algorithm development. The candidate is responsible for designing, simulating, and implementing performance enhancing signal processing algorithms used in ABIOMED’s family of products. We are looking for a motivated and energetic self-starter, has a ‘make it happen’ attitude, and can thrive in a fast-paced, cutting edge environment. etc. | 9/10/2019 |
| 14040 | AbSci Vancouver, WA Research Associate I BS in molecular biology, biochemistry, microbiology or related Exp: 1-2 years |
The Research Associate I, under direction of the Molecular Sciences team, will support innovative experimental research that advances AbSci’s proprietary E. coli expression platform. Primary responsibilities include providing core support to ongoing DNA construction, strain engineering, and small-scale protein expression activities. Daily activities will include management of the Molecular Sciences laboratory consumables and sample libraries, preparation of common research reagents, and providing assistance to ongoing experiments. The ideal candidate will demonstrate rapid mastery of assigned tasks and the capacity to take on additional technical responsibilities within an expanding team. | 9/10/2019 |
| 14041 | AbSci Vancouver, WA Research Associate I, Protein Purification BS/MS in biochemistry or related Exp: 1-4 years |
The Research Associate I will play a significant role in purification of protein biologics, and report to the Purification Group Leader. Core responsibilities include maintaining and operating chromatography instrumentation, conducting hands-on research for development of new techniques, and supporting ongoing protein purification activities. The ideal candidate will have a passion for scientific innovation, excellent technical skills, execute their responsibilities with high attention to detail, and work well within a team dynamic in a high-performance culture. etc. | 9/10/2019 |
| 14042 | Absorption Systems Medford, MA Research Associate - Bioanalytical BS/BA in a scientific field Exp: 1+ years |
The Research Associate will work as part of a team in a lab environment to completeclient-driven projects. Primary responsibilities include: Perform sample analysis following established SOPs underRUO/GLP/GMP conditions. Assist in the development and validation of new assays. General laboratory tasks including buffer preparation, samplelogging and handing, shipping samples to or for clients, equipment maintenance,lab maintenance, and ordering supplies. Ensuring the accuracy and timeliness of all laboratory-relatedprocesses. etc. | 9/10/2019 |
| 14043 | Absorption Systems Exton, PA Associate Scientist / Scientist – Molecular Biology & Gene Expression – GMP BS/MS Exp: BS: 1-3 years, MS: under 2 years |
Absorption Systems, provides analytical support for gene and cell therapy products through every stage of development, is seeking a candidate for either an Associate Scientist or Scientist position with GMP experience in molecular biology and gene expression at the headquarter location in Exton, Pennsylvania. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. etc. | 9/10/2019 |
| 14044 | Absorption Systems San Diego, CA Research Associate – Bioanalytical BS in chemistry or related Exp: 0-1 years |
The Research Associate, Bioanalytical will provide bioanalytical quantitative analysis of test compounds in biological matrices obtained from a variety of studies including preclinical safety evaluations and pharmacokinetic evaluations. Focus on small molecule analysis using LC-MS/MS. Principal Duties and Responsibilities: Execute experiments by LC-MS/MS in support of drug discovery and early development programs following the SOP. The candidate will be responsible for sample preparation from biological matrices, tissue homogenization, sample extraction techniques, and data acquisition. Perform duties in a timely manner to achieve study timelines. Perform other duties as directed by Management. etc. | 9/10/2019 |
| 14045 | Absorption Systems Exton, PA Associate Scientist / Scientist – Drug Transport & Metabolism BS/MS Exp: BS: 1-3 years, MS: under 2 years |
Absorption Systems provides analytical support for gene and cell therapy products through every stage of development. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. Absorption Systems is seeking a candidate for either an Associate Scientist or Scientist position with drug transport and metabolism experience at the headquarter location in Exton, Pennsylvania. etc. | 9/10/2019 |
| 14046 | Accelerate Diagnostics Tuscon, AZ Aseptic Filling Technician HS diploma/AS/BS Exp: 1+ years |
The Fill Technician will perform a variety of processing duties according to Batch Records (BRs) and Manufacturing Work Instructions (MWIs) in a cGMP environment for the Consumable Manufacturing Department including, but not limited to: Cleaning/recovery of classified area and work spaces, components preparation. Aseptic filling. Final Consumable Inspection. Labeling and packaging. Line clearance and Closeout responsibilities. etc. | 9/10/2019 |
| 14047 | Accelerate Diagnostics Tuscon, AZ Quality Control Technician BS in microbiology, chemistry, molecular and cell biology, or related Exp: 1+ years |
The Quality Control Technician will join Accelerate Diagnostics’ Consumable Operations team. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, spectrophotometer, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. etc. | 9/10/2019 |
| 14048 | 10x Genomics Pleasanton, CA Research Associate-Process Development (Temp) BS/MS in chemistry, chemical engineering, microfluidics, or equivalent Exp: 0-5 years |
10x is seeking an outstanding Research Associate to join work on the rapid prototyping and testing of critical 10x reagents. This individual will be involved in developing and validating consumables for the rapid expansion of 10x product lines. This role requires excellent laboratory skills and attention to detail with demonstrated success in executing operations consistently. Individuals applying for this position must be self-starters, strategic thinkers, action driven, flexible in changing direction and methods, thrive in a fast-paced environment, excel at managing multiple priorities, succeed in communicating with all levels within the organization and provide immediate contribution. etc. | 9/10/2019 |
| 14049 | Ajinomoto San Diego, CA QC Logistics Assistant HS Diploma or BS/BA Exp: 0-2 years in QC |
In this role you will play a big part in keeping our sample testing processes running smoothing by managing sample submission, receipt, and shipping coordination of all incoming test articles into Quality Control. You may focus in a specialized area and provide routine analysis and testing according to standard operating procedures for in-process and finished formulations. | 9/7/2019 |
| 14050 | Ajinomoto San Diego, CA QA Batch Release Assistant HS Diploma or BS/BA Exp: 0-2 years in QA |
The QA Batch Release Assistant ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. They have the ability to work independently, within prescribed guidelines, and as a team member. The Assistant promotes a cGMP environment and follows all Standard Operation Procedures (SOP’s). | 9/7/2019 |
| 14051 | Ajinomoto San Diego, CA MQA Assistant HS Diploma or BS/BA Exp: 0-2 years in QA |
he MQA Assistant ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. This individual has the ability to work independently, within prescribed guidelines, and as a team member. This position promotes a cGMP environment and follows SOPs. | 9/7/2019 |
| 14052 | Ajinomoto San Diego, CA Drug Substance Manufacturing Associate I - Upstream HS Diploma or BS/BA Exp: 0-2 years in upstream biologics manufacturing |
This position, under supervision, is responsible for executing the day to day responsibilities related to the Drug Substance Manufacturing Upstream group under the guidance of Aji Bio-Pharma's established procedures and policies. The position works under the guidance of experienced team members in support of the technical transfer and integration of processes into the Drug Substance Manufacturing Upstream department. The position will be exposed to fermentation, harvest, and TFF (UF/DF) systems employed during manufacturing campaigns. | 9/7/2019 |
| 14053 | Ajinomoto San Diego, CA Drug Product Inspection Technician HS Diploma or BS/BA Exp: 0-2 years in lab/manufacturing |
In this role you will be responsible for performing a wide variety of product inspection and packaging tasks. You will complete training and pass qualification testing for visual inspection of various product forms, perform accurate visual inspection and handling of products following SOPs while working under cGMP regulations. | 9/7/2019 |
| 14054 | Akorn Decatur, IL 1st shift QA Technician I, Documentation Systems One year certificate from college/tech school Exp: 0-1 years |
Revise and maintain controlled documents including, but not limited to: Master Batch Records, Standard Operating Procedures, Active Pharmaceutical Ingredient Specifications, Finished Drug Product Specifications, Forms, and Protocols. Maintain and distribute Document Change Requests. Provide coverage for Front Desk. | 9/7/2019 |
| 14055 | Akorn Decatur, IL Technical Development Engineer BS/BA in chemical/mechanical/systems engineering Exp: Entry Level |
The full-time, Development Engineer will have an opportunity to rotate through 3 areas of engineering within our Decatur, IL facility during their first year of employment – Maintenance, Projects and Technical. | 9/7/2019 |
| 14056 | Akorn Vernon Hills, IL Formulation Scientist I BS/MS/PhD in pharma sciences or related Exp: 1 or more years |
We seek a talented Formulation Scientist to join our expanding R&D team who will be responsible for developing the final product formulation, process procedures and packaging of semisolids, suspensions and solutions, lotions, nasal sprays, inhalations, sterile injectable and ophthalmic products etc. Literature searching and review, patent searching and interpretation, performing risk assessment for formulation/process development, conducting experimental design and execution of lab scale, pilot scale developmental batches to support the final formulation and processes. | 9/7/2019 |
| 14057 | Akorn Decatur, IL 2nd shift QA Technician I, Documentation Systems One year certificate from college/tech school Exp: 0-1 years |
Revise and maintain controlled documents including, but not limited to: Master Batch Records, Standard Operating Procedures, Active Pharmaceutical Ingredient Specifications, Finished Drug Product Specifications, Forms, and Protocols. Maintain and distribute Document Change Requests. Provide coverage for Front Desk. | 9/7/2019 |
| 14058 | Akorn Decatur, IL 2nd shift Chemist I BS/BA in chemistry/chemical engineering Exp: 0-2 years, experience prefered |
The quality control chemists perform testing on raw materials, bulk formulations, finished products, stability samples, and any other samples from plant operations that require chemical analysis. The QC chemists report to the QC manager. Responsible for the laboratory testing in accordance with company SOP’s as well as cGMP’s and GLP’s. Testing involves Raw materials, In-process, Finished product, and Stability samples for potency and physical characteristics such as pH, Specific gravity, Moisture, etc. | 9/7/2019 |
| 14059 | Akoya Biosciences Menlo Park, MA Application Scientist, Contract Research Services MS in life sciences Exp: 0-2 years |
Akoyais seeking an experienced Scientist to join our Quantitative Pathology Solutions –Phenoptics Services (QPS-PS), Image Analysis teamlocatedin Hopkinton, MA. Akoyaenables staining with up to eightantibodies utilizing our OPAL™ technology to provide unparalleled cellular/tissue imaging capabilities. QPS-PS is a dynamic team that develops multiplex OPAL™ panels for clients, then performs staining, imaging, and quantitative analysis of their samples. The QPS-PS Image Analysisteam focuses on imaging of stained slides and image analysis. | 9/7/2019 |
| 14060 | Absorption Systems Exton, PA Associate Scientist - Drug Transport & Metabolism BS/BA or MS in related Exp: BS: 1-3 years, MS: 0-2 years |
Absorption Systems is seeking a candidate for either an Associate Scientist or Scientist position with drug transport and metabolism experience at the headquarter location in Exton, Pennsylvania. Conduct study projects: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. Conduct studies on different assays, such as drug transport, metabolism and CYP induction assays | 9/6/2019 |
| 14061 | Absorption Systems San Diego, CA Research Associate – Bioanalytical BS in chemistry, biochemistry, or related Exp: 0-1 years |
The Research Associate, Bioanalytical will provide bioanalytical quantitative analysis of test compounds in biological matrices obtained from a variety of studies including preclinical safety evaluations and pharmacokinetic evaluations. Focus on small molecule analysis using LC-MS/MS. The candidate will be responsible for sample preparation from biological matrices, tissue homogenization, sample extraction techniques, and data acquisition. | 9/6/2019 |
| 14062 | Absorption Systems Medford, MA Research Associate – Bioanalytical BS/BA in sciences Exp: 1+ years in industry |
TheResearch Associate will work as part of a team in a lab environment to completeclient-driven projects. Primaryresponsibilities include: Perform sample analysis following established SOPs underRUO/GLP/GMP conditions, Assist in the development and validation of new assays., General laboratory tasks including buffer preparation, samplelogging and handing, shipping samples to or for clients, equipment maintenance,lab maintenance, and ordering supplies | 9/6/2019 |
| 14063 | Accelerate Diagnostics Tuscon , AZ Quality Control Technician BS in biological sciences or chemistry Exp: 1+ years in lab/research |
The Quality Control Technician will join Accelerate Diagnostics’ Consumable Operations team. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, spectrophotometer, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basisThe Quality Control Technician will join Accelerate Diagnostics’ Consumable Operations team. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, spectrophotometer, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basisThe Quality Control Technician will join Accelerate Diagnostics’ Consumable Operations team. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, spectrophotometer, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis | 9/6/2019 |
| 14064 | Acceleron Cambridge, MA Research Associate, Cell Culture and Media Prep BS or MS in cell biology Exp: 1 or more years in lab |
We are seeking a highly organized, motivated individual with experience in media and buffer preparation, mammalian cell culture, and recombinant protein expression. You will contribute to the development of our next-generation biologic therapeutics by generating cell lines and analyzing recombinant proteins. You will work cross-functionally with the Molecular Biology, Protein Purification, and Process Development groups and will have the opportunity to gain experience in multiple aspects of drug development. | 9/6/2019 |
| 14065 | Accuray Madison, WI Temporary Product Surveillance Specialist BS in engineering or clinical field Exp: 0-3 years |
The Product Surveillance Specialist effectively implements the complaint handling process and processes complaints in a uniform and timely manner according to regulatory requirements and company practices and policies. Evaluates complaints to determine whether an investigation is necessary and if Medical Device Reporting (MDR) is necessary in accordance with 21 CFR Part 803 Medical Device Reporting and 806 Corrections and Removals, Canadian regulations, European Vigilance Reporting and any other worldwide regulatory requirements. | 9/6/2019 |
| 14066 | KCI South Burlington, VT Field Service Representative I HS Diploma/GED Exp: 1 year work experience |
This position is responsible for providing world class customer service during the provision, return and servicing of medical equipment inclusive of responding to product inquiries or other identified customer needs. The daily responsibilities encompass the preparation of medical equipment for patient use to include sanitization and disinfection, quality control testing, preparation for use and transportation of the equipment to and from customer locations utilizing a company provided vehicle. | 9/6/2019 |
| 14067 | KCI Dillon, CO Appeals Specialist I HS Diploma/GED Exp: 1 year work experience |
Provide lead with work progress reports on a daily, weekly, monthly basis or as required Investigate and analyze patient charts and wound progress reports, by reading documents and negotiating computer-based research To develop, for each Medicare Insurance claim denial, a reasonable patient product use detail and history; to develop and substantiate the product use evidence, and present the patient’s case to Medicare in the manner required or make appropriate adjustments Write a medically concise and issue focused Redetermination, Reconsideration, or Administrative Law Judge letter as required as it applies to Medicare policy | 9/6/2019 |
| 14068 | KCI San Antonio, TX Quality Engineer I BS in mechanical/biomed/industrial engineering Exp: Entry Level |
The Quality Engineer I is responsible for conducting, and reporting on product, project and process activities related to medical device design and manufacturing as a team member. This position works with R&D and Manufacturing to develop and execute test protocols and reports. This position performs statistical analysis as required. The Quality Engineer I and works closely with R&D, Supplier Quality, Sustaining Engineering, and Manufacturing to ensure effective design transfer and successful on-going manufacturing. | 9/6/2019 |
| 14069 | KCI Virginia Beach, VA Associate Territory Representative -- Medical Device Sales BS/BA Exp: 0-2 years |
The Associate Territory Representative (ATR) is the main point of contact on transition related sales activities. The role will focus on proactively generating sales revenue from transitions and coordinating with the Advantage Center on necessary paperwork relating to transition sales. The ATR will round floors on a daily basis to make sales and generate leads under the direction of the District Manager. The ATR will assist with account management activities including the setup of READYCARE and KCI Express and assist customers with invoicing, credit and collection issues, as well as conduct inventory management to recover lost assets. | 9/6/2019 |
| 14070 | WCG Clinical Plymouth Meeting, PA Feasibility Specialist BS/BA in health care or scientific discipline Exp: 6 months of admin experience for projects |
The Feasibility Specialist is responsible for implementing site start-up activities during the Site Feasibility Questionnaire (SFQ) collection process. Coordinate project management activities, resources, equipment and information to support client and Company for project/service solutions. Liaise with clients to identify and define requirements and objectives. | 9/6/2019 |
| 14071 | Actuated Medical Bellefonte, PA Clinical Education Specialist 4 year or 2 year business degree Exp: 0-3 years |
The relevant experience required for a Clinical Education Specialist (CES) is a four year business degree or significant experience working with marketing activities, specifically digital marketing. The CES must possess a working knowledge of business principles, schedule management, organizational styles and marketing practices. The CES has the responsibility of supporting the Clinical Education Leader, President, and Director, R&D to move the company Up and Onward. The CES must assist to position Actuated Medical (AMI) as a company that Improves Patient Outcomes by developing Innovative Motion® Medical devices and providing clinical education to improve patient care. | 9/6/2019 |
| 14072 | Emergent BioSolutions Camden, MD Assistant Technician, Inspection & Packaging HS Diploma/GED Exp: 0-2 years |
This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. Execute and document procedural steps in compliance with cGMP standards. Perform 100% visual inspection of product and classify rejected materials utilizing approved categories within required timelines (Qualification). Package product in final packaging components while verifying that lot information, including lot number and expiration date, are accurate | 9/6/2019 |
| 14073 | Emergent BioSolutions Camden, MD Assistant Technician, Inspection & Packaging HS Diploma/GED Exp: 0-2 years |
This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. Execute and document procedural steps in compliance with cGMP standards. Perform 100% visual inspection of product and classify rejected materials utilizing approved categories within required timelines (Qualification). Package product in final packaging components while verifying that lot information, including lot number and expiration date, are accurate | 9/6/2019 |
| 14074 | Emergent BioSolutions Bayview, MD Manufacturing Associate II HS Diploma/GED required, BS preferred Exp: 1 or more year in GMP |
The Manufacturing Associate II position reports to Manager Manufacturing at Emergent Manufacturing Operations Baltimore (EMOB). Prior experience in GMP manufacturing and operation of GMP process equipment are prerequisites. Operates manufacturing equipment such as: incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in process testing equipment | 9/6/2019 |
| 14075 | Emergent BioSolutions Lansing, MI Assistant Manufacturing Associate HS Diploma/GED Exp: 0-1 years in cGMP |
Execute tasks per cGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing qualification block training program. Actively incorporate the Core Values set out by Emergent BioSolutions while performing day to day activities. | 9/6/2019 |
| 14076 | Emergent BioSolutions Camden, MD Analyst I, QC 2nd shift BS in chemistry or related Exp: 0-2 years in GMP lab |
Perform analytical testing per cGMP in support of raw material, in-process, final product, stability. Typical hours are 2:00pm – 10:30pm, Monday through Friday. Hours may vary to meet business and training needs. Perform WFI sampling and testing as per current protocol, or validation protocols to support the WFI system. Perform various analytical testing procedures as per manufacturing/quality control batch records, stability protocols, raw material requests for testing, etc. | 9/6/2019 |
| 14077 | Emergent BioSolutions Bayview, MD Analyst I, QC AS/AA in biological sciences Exp: 1-3 years in pharma/biotech |
The Quality Control Analyst I, Microbiologist position supports the Quality Control group at EMOB to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the EMOB Microbiology, Environmental Monitoring, and Clean Utility testing programs, microbiological product testing, and supporting quality initiatives. Ensures samples are collected, tested, and reported per associated procedures and methods. Responsible for quality document generation and revision, and quality notification execution. | 9/6/2019 |
| 14078 | Emergent BioSolutions Canton, MA Analyst I, QC Microbiology BS/BA in applied sciences Exp: 0-2 years |
This is a laboratory testing position with the major responsibilities being daily routine EM and Micro testing, and laboratory maintenance/upkeep tasks. Additional responsibilities involve quality systems support which includes supporting laboratory investigations as appropriate. Works with facilities/metrology to conduct and document execution of work orders to ensure GMP compliant state of labs and equipment. Performs routine EM and Micro testing following written procedures and limited non-routine testing including validation studies with supervisory oversight. | 9/6/2019 |
| 14079 | Adaptive Biotechnologies Seattle, WA Facilities and Equipment Coordinator BS/BA in engineering/sciences Exp: 1 or more year in lab |
The Facilities and Equipment Coordinator will serve the Facilities Department at the Adaptive Biotechnologies Seattle location. The primary function of this role is to support laboratory and building services including equipment maintenance and calibrations, equipment records, qualifications (IQ/OQ/PQ), and vendor coordination’s for the regulated and non-regulated lab space. This individual will provide cross-functional support for critical revenue driving assets and departments including the Production, Clinical Development, and Research Labs. | 9/6/2019 |
| 14080 | Adaptive Biotechnologies Seattle, WA Lab Operations Compliance Specialist BS in biological sciences Exp: 1 or more year in quality management systems |
The Lab Operations QA/compliance Specialist supports activities in the Operations group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support the QA/Compliance activities for the CAP/CLIA/NYS regulated laboratory, related to the services provided. | 9/6/2019 |
| 14081 | Qdare Pharmaceuticals Vandalia, OH Operator I HS Diploma/GED Exp: Entry Level |
The essential job function are to produce specified products by the mixing, blending, and combining of raw materials as specified by written procedures. This position is night shift working 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday. | 9/6/2019 |
| 14082 | Qdare Pharmaceuticals Vandalia, OH Operator I HS Diploma/GED Exp: Entry Level |
The essential job function are to produce specified products by the mixing, blending, and combining of raw materials as specified by written procedures. This position is night shift working 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday. | 9/6/2019 |
| 14083 | Adimab Lebanon, NH Research Associate - Protein Analytics BS in biological sciences or chemistry/engineering Exp: 0-2 years |
The Research Associate will work in a small team setting to support Adimab’s novel antibody discovery, maturation, and production platform. This role will closely interface with the Antibody Discovery, High Throughput Expression, Molecular Core, and Computational Biology teams. Assist in in-process antibody characterization, including ForteBio kinetics and binning. Run biochemical/biophysical assays, including but not limited to, Tm and endotoxin. | 9/6/2019 |
| 14084 | ADMA Biologics Boca Raton, FL QC Lab Support Associate l BS in biology, chemistry, medical technology Exp: 1-3 years in regulated lab setting |
The QC Lab Support Associate I will Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. Customer support functions for QC laboratories such as cleaning glassware and custodial services, monitoring temperature controlled chambers, shipping samples, sample preparation, administrative support. | 9/6/2019 |
| 14085 | ADMA Biologics Boca Raton, FL QC Raw Materials Specialist BS or AS in chemistry/biochemistry/biology Exp: 0-3 years |
The Raw Material Specialist I will Perform quality control raw material processing and testing. Following general instructions on routine work and detailed instructions on new assignments. Perform quality control raw material processing, sampling and testing independently according to approved Standard Operating Procedures. Complete testing documentation and data entry as required for procedures and tests performed in-house and at contract labs. | 9/6/2019 |
| 14086 | ADMA Biologics Boca Raton, FL Document Assistant - Temporary Some college Exp: 1-2 years |
The Document Assistant will Create, format, revise and proof read controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control. Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies. | 9/6/2019 |
| 14087 | ADMA Biologics Boca Raton, FL Technician I, Manufacturing Purification BS/BA in life sciences/chemistry Exp: 0-2 years |
It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. | 9/6/2019 |
| 14088 | Sonova Aurora, IL Production Associate I - 2nd shift HS Diploma/GED Exp: 1-3 years |
The Production Associate I will perform manufacturing functions associated with the following: Assembly, service and testing of BTE, RIC and FM systems. Assembly and testing of ITE custom hearing aids, Slim-tips, C-Shells and Ear Molds. Visual inspects product, identifies defects/rejects and escalates as required. Performs general routine machine maintenance and daily workstation clean-up | 9/6/2019 |
| 14089 | Sonova Valencia, CA Quality Control Inspector I HS Diploma/GED Exp: 1-2 years in inspection |
Responsible for performing visual, mechanical and electrical inspections at subassembly and final assembly levels. Perform visual and mechanical inspections at sub-assembly and final assembly levels, using engineering drawings/specifications and general quality control standards. Review manufacturing documentation to ensure that all assembly, testing and inspection steps were performed in accordance to specifications. | 9/6/2019 |
| 14090 | Sonova Warrneville, IL Customer Service Representative II HS Diploma/GED Exp: 1-2 years |
Handle customer complaints with a sense of urgency for satisfactory resolution and take ownership of that complaint. To use the current tools (SAP, Sales Force, and Cisco Finesse) to generate and maintain all customer account records and customer contacts. Handle customer requests by email and phone | 9/6/2019 |
| 14091 | Bio-Techne San Jose, CA Manufacturing Laboratory Technician AA degree Exp: 1+ years of lab/manufacturing experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Key responsibilities include: Assemble reagents and consumables kits, Perform in-process QC and record results, Document production batch records/travelers, and computer data entry, etc. | 9/6/2019 |
| 14092 | Bio-Techne San Marcos, CA Chemist I, R&D BS/BA in chemistry, biochemistry, or biological sciences Exp: 1-5 years work in in vitro diagnostics/biotech |
Responsible for developing controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for developing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to research in a laboratory environment. | 9/6/2019 |
| 14093 | Bio-Techne Minneapolis, MN Production Assistant 1 HS Diploma/GED Exp: 0-2 years lab experience |
As a Production Assistant 1, you will be responsible for the processing of raw biological material for use in product manufacturing. You will also perform maintenance and cleaning of production equipment and containers to ensure safety and compliance, as well as completing required paperwork. | 9/6/2019 |
| 14094 | Bio-Techne Minneapolis, MN Lab Assistant I HS Diploma/GED Exp: 0-2 years |
The responsibilities of this position are to perform lab support duties and tasks for multiple departments that include: collecting and washing used labware, preparing the labware for the autoclave, running the autoclave, and harvesting and concentration of cell culture media. Perform additional duties as assigned. This position requires a Tuesday through Saturday schedule. | 9/6/2019 |
| 14095 | Bio-Techne San Jose, CA Manufacturing Laboratory Technician AA degree Exp: 1+ years of lab/manufacturing experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Operate and maintain robotic and manufacturing equipment, Document production batch records/travelers, and computer data entry, Perform in-process QC and record results | 9/6/2019 |
| 14096 | Bio-Techne Minneapolis, MN Product Receiving Associate HS Diploma/GED Exp: 0-2 years |
Product Receiving Associate is responsible for the receipt and delivery items from outside vendors, throughout the campus. These deliveries include materials that are of critical and temperature sensitive nature. Product Receiving Associates assist with maintaining and delivering items located in the company stores warehouse. This role works with PO data housed in our ERP system. This role will perform driving duties using company owned vehicles. Perform additional duties as assigned. | 9/6/2019 |
| 14097 | Bio-Techne San Marcos, CA QC Specialist 1 BS/BA in biological sciences or chemistry Exp: 1-2 years in in vitro diagnostics/biotech |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. Coordinate, perform and maintain QC testing and scheduling for Stability program, Assist in establishing QC specifications, Assist in the validation testing of equipment and processes, etc. | 9/6/2019 |
| 14098 | Adverum Biotechnologies Menlo Park, CA Associate I, Quality Control BS in sciences Exp: 0-2 years in analytical, cGMP or health lab |
This individual will support the Quality Control team through development and performance Quality Control (QC) systems, policies, processes, procedures and controls as they relate to the analytical testing of clinical materials. Perform regular laboratory and equipment cleaning and maintenance according to standard operating procedures (SOPs). | 9/6/2019 |
| 14099 | CAPS Phoenix, AZ Pharmacy Technician HS Diploma/GED Exp: 1 or more years in aseptic preperation |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Responsibilities include: Prepares compounded sterile products using aseptic technique. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. | 9/6/2019 |
| 14100 | AGC Biologics Bothell, WA Manufacturing Associate I-IV - Upstream BS in chemistry, biology, or related Exp: 1-4 years, with experience in aseptic processing |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. | 9/6/2019 |
| 14101 | AGC Biologics Bothell, WA Manufacturing Associate I - Downstream BS in chemistry, biology, or related Exp: 1-8 years, depending on level |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Clean, assemble/disassemble, sterilize and operate primary process equipment. etc. | 9/6/2019 |
| 14102 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I-IV BS in chemistry, biology, or related Exp: 1-8 years, depending on level |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Clean, assemble/disassemble, sterilize and operate primary process equipment. etc. | 9/6/2019 |
| 14103 | AGC Biologics Bothell, WA Development Associate I - II A.A./B.S. in a life science or engineering Exp: 0-2 years |
This is a Development Associate I position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures | 9/6/2019 |
| 14104 | AGC Biologics Bothell, WA Development Associate I (Contract, Temp-to-Perm) Sun-Wed A.A./B.S. in a life science or engineering Exp: 0-3 years |
This is a Development Associates position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. | 9/6/2019 |
| 14105 | AGC Biologics Bothell, WA Development Associate I (Contract, Temp-to-Perm) Monday-Friday HS Diploma or Aa in life science/engineering Exp: 0-3 years |
This is a Development Technician position in the Process Development Support group. Primary responsibility will be to support the process development team processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for lab support. Under general supervision, this person carries out routine to moderately complex lab operations. | 9/6/2019 |
| 14106 | Agilent Wilmington, DE Analytical Instruments Technical Support BS/BA in chemistry or life sciences Exp: Entry Level |
As an Analytical Instruments Technical Support person, you will sit at our Agilent site in WIlmington, DE and join Agilent Technologies CrossLab Group's Online Technical Support Team. We support U.S. external customers. As an active team member, you will support customers requesting hardware, software and applications assistance with Analytical Products and Solutions and route those customers whom you can't help to the appropriate groups. Our group's organizational goal is that as part of a world-class technical support group, we provide insights to customers at their very first contact. In order to be successful, our response needs to be quick and well-informed. | 9/6/2019 |
| 14107 | Agilent Wilmington, DE R&D Electrical Engineer BS or MS in electrical engineering or related Exp: Entry Level |
As an Electrical Engineer in our R&D group, you'll be part of a team that analyze, design, prototype and test new products for Agilent's Gas Chromatograph, Automated Sample Handling and Automated Sample Preparation products. Most projects require mechanical, electrical and firmware engineers, as well as chemists and software engineers, to create a complete system. As part of those projects, you will also work with our marketing, manufacturing, purchasing and service organizations to transform your designs into shipping products. | 9/6/2019 |
| 14108 | Agios Cambridge, MA Associate, Commercial Supply Chain BS in business/supply chain/management Exp: 1 year or more in GMP |
Agios Pharmaceuticals is searching for a dynamic Associate, Commercial Supply Chain to join our growing Supply Chain team. The selected individual will have full exposure across early clinical space to regular commercial production activities and exposure to new commercial product launches. With support from Commercial Supply Chain Management, oversee timelines for both internal activities and external production activities at Contract Manufacturing Organizations (CMOs) to ensure continuous supply of Commercial and Clinical materials through the supply chain. | 9/6/2019 |
| 14109 | Wright Cleveland, OH Associate Sales Representative, Upper Extremities BS/BA Exp: 0-2 years |
This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is a field based position. | 9/3/2019 |
| 14110 | Wright St. Louis, MO Sales Support Associate - St. Louis, MO HS diploma Exp: 0-2 years |
Wright Medical is currently hiring a Sales Support Associate. The Sales Support Associate will be responsible for assisting in the successful execution of the sales plan for their assigned territory and the achievement of quarterly and annual sales plan objectives. He/she will travel within the territory and region for development & sales support. He/she will maintain open communications with their assigned leadership team and headquarter based sales training leader. He/she will perform and excel in case coverage, sales territory support functions and sales activity. He/she will achieve success with specified individual training and development plan. etc. | 9/3/2019 |
| 14111 | Wright Alexandria, LA Sales Support Associate - Alexandria, LA HS diploma Exp: 0-2 years |
Wright Medical is currently hiring a Sales Support Associate. The Sales Support Associate will be responsible for assisting in the successful execution of the sales plan for their assigned territory and the achievement of quarterly and annual sales plan objectives. He/she will travel within the territory and region for development & sales support. He/she will maintain open communications with their assigned leadership team and headquarter based sales training leader. He/she will perform and excel in case coverage, sales territory support functions and sales activity. He/she will achieve success with specified individual training and development plan. | 9/3/2019 |
| 14112 | Wright Phoenix, AZ Associate Sales Rep, Lower Extremities and Biologics BS/BA Exp: 0 years |
This position is responsible for assisting Sales Representatives in the district with the successful execution of sales plans for their assigned areas and the achievement of quarterly and annual sales plan objectives. This role includes essential functions such as the management of field sales operations, customer acquisition, cultivation & retention, product launch execution, inventory management, surgical case coverage, and travel within the district as well as maintaining open communications with their district leader. This is a field based position. | 9/3/2019 |
| 14113 | Wright Bloomington, MN Shipping Clerk I HS diploma or equivalent Exp: 0-1 years |
The responsibilities of the Shipping Clerk I are to pull, check, pack, and ship Wright Medical products within the U.S. borders. The Shipping Clerk will operate the Fedex, UPS, and Powership stations to process packages and help protect the integrity of Wright Medical inventories. Essential Job Functions: Process orders based on the external customers preferred shipping system (e.g. USPS, UPS, FedEx, etc.) Prepare and print shipping labels corresponding to shipping needs. Assemble and fill boxes and other cartons with items that need to be shipped. etc. | 9/3/2019 |
| 14114 | Wright Portland, OR Inventory & Sales Support Handler HS diploma or equivalent Exp: 1-3 years |
The Inventory & Sales Support Handler ensures the timely processing of kits/sets in the remote location. This could include, but is not limited to, checking in sets, verifying completeness, restocking, creating new kits from sterile implant SKUs, and other basic set maintenance. The Inventory & Sales Support Handler is required to function with minimal supervision to ensure that work flow is uninterrupted and that all customer requirements are met within the functional area. The Inventory & Sales Support Handler will ensure that all relationship and delivery functions are carried out timely and as needed. Driving abstracts will be required every year to ensure certification for driving company van. etc. | 9/3/2019 |
| 14115 | WuXi AppTec Philadelphia, PA Associate Scientist - Genetic Stability MS in biological sciences or related Exp: None required for MS candidates |
Independent scientist who demonstrates innovative technical knowledge and significantly contributes to the overall operations of the lab. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and documentation. Demonstrates supervisory skills and contributes to the achievement of company and departmental goals and objectives. Performs and directs Genetic Stability assays, especially Southern Blotting, according to and in compliance with current Good Manufacturing Practice (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). etc. | 9/3/2019 |
| 14116 | WuXi AppTec Philadelphia, PA Laboratory Technician II Monday through Friday; Second Shift BS in biological science or related Exp: 1-2 years |
Performs Cell Culture and Cell-Based assays (BSL2 and BSL2+) according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Completes batch records and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs daily work activities with minimal supervision. etc. | 9/3/2019 |
| 14117 | WuXi AppTec Philadelphia, PA Laboratory Technician I BS in biological science or related Exp: 1-2 years |
Performs assays according to testing records and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under direct supervision, completes test methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. etc. | 9/3/2019 |
| 14118 | Zoetis Salisbury, MD Production Operator HS diploma or equivalent Exp: 6 months |
This position is responsible for operating process equipment and following all site operating, Quality, cGMP, and safety procedures associated with manufacturing of bulk medicated feed additives (MFA) from raw material to finished product. Incumbent must be able to clearly and frequently communicate with various functions within the site, including production, maintenance, quality operations, fermentation development, and administration. etc. | 9/3/2019 |
| 14119 | Zoetis Kalamazoo, MI Packaging Technician Assistant (2nd and 3rd Shift) HS diploma or equivalent Exp: 6-12 months |
Work as part of a team operating pharmaceutical packaging lines. Operate packaging equipment and other related tasks. Maintain accurate and concurrent documentation of all tasks completed. Maintain a positive attitude and be able to work well with others in a team environment. Demonstrate good attendance. A Packaging Technician Assistant works as part of a team in a complex, integrated, production environment. The individual(s) selected will have attention to detail, a positive attitude, a strong work ethic, and the ability work well with others in a team environment. etc. | 9/3/2019 |
| 14120 | Zoetis Union City, CA Instrument Manufacturing Technician I HS diploma or equivalent Exp: Entry level |
Assemble and test Point of Care medical Instruments. Process instruments according to all applicable procedures and quality requirements. Major Duties and Responsibilities – including but not limited to: Follow detailed operating procedures to assemble and test point of care medical instruments. Maintain productivity and quality requirements. Operate safely within a biohazardous environment. | 9/3/2019 |
| 14121 | Zoetis Kalamazoo, MI Customer Support Associate - Technical Analyst BS/BA Exp: 1+ years |
Interface with internal and external customers from multiple departments and levels of management to achieve the business’ sales and product delivery objectives. Responsible for system support and automation to provide improved data delivery and efficiency in processes. Participate in communications with relevant breed associations and other stakeholders at an operational level to ensure seamless delivery of contracted services related to systems and reporting. Lead projects focused on Process Improvement, system integration and/or data delivery, as directed by Team Lead and/or Manager. Cooperate with the Quality and Product Delivery Team (Global Genetics) to provide support to internal investigations and new product delivery. Contribute to a team culture of continuous process improvement. etc. | 9/3/2019 |
| 14122 | Zymergen Emeryville, CA Research Associate, Microbial Genome Engineering BS/MS Exp: 0-2+ years |
Zymergen is hiring a distinctive Research Associate to develop technologies for high throughput DNA assembly and engineering of microbial genomes. The Research Associate will help create new technologies, bring in cutting edge protocols, and improve existing Zymergen protocols to provide newer and better workflows to our microbe engineering Factory. At Zymergen, the Research Associate will work together with other scientists, automation engineers, and software engineers to develop protocols for DNA cloning and microbial strain engineering, and then enable their use in high throughput workflows. etc. | 9/3/2019 |
| 14123 | Zymergen Emeryville, CA Chemist, Polymer Chemist BS/MS in chemistry, materials science, or related Exp: 1-2 years |
Zymergen is looking for a chemist with training and experience in polymer synthesis and characterization. The candidate will be a key contributor to the polymer synthesis efforts, i.e. polymer development at the discovery stage, related to our film products. He or she will be responsible for purifying and performing quality control on reagents, performing step-growth polymerizations, optimizing reaction conditions, casting films and testing basic polymer material properties. The candidate will work closely with the project scientists to help drive the overall program progress on a technical level. etc. | 9/3/2019 |
| 14124 | Zymergen Emeryville, CA Inventory Technician I HS diploma or equivalent Exp: 1-3 years |
This position requires the ability to execute daily tasks/requests with promptness and prioritize work in a fast pace environment. An ideal candidate for this position is organized, diligent, and displays excellent customer service skills. Job Description and Specific Responsibilities: Organizing and maintaining an inventory of laboratory supplies throughout the labs. Ensures material is available according to the production schedule. Performing daily cycle counts of designated inventory areas. Receive and verify material on a daily basis. etc. | 9/3/2019 |
| 14125 | Zymergen Emeryville, CA Research Associate, Fermentation Development MS Exp: None required for MS candidates |
Zymergen is hiring Research Associate into the Test Centers of Excellence team to focus on the continual improvement of both high throughput screening and fermentation workflows. These associates are required to be able to identify and implement improvements in existing processes and establish protocols for new programs. This person will need to know microbial metabolism and physiology, microbial culture techniques (including fermentation and screening methods). Assay development experience would be useful, as well as experience with Tecans, but this would be part of the training. etc. | 9/3/2019 |
| 14126 | Zymo Research Irvine, CA Research Associate/Tech Support Specialist MS in biology, biochemistry or related Exp: None required for MS candidates |
We are seeking highly-motivated and proactive individuals to join our R&D team as a Research Associate. Working side by side with some of the most talented people in biotechnology, the successful applicant will participate in independent product research efforts targeted at driving either the development of novel, cutting-edge technology or improvements to products currently in our portfolio. The incumbent will have demonstrated clear leadership potential with ability to efficiently multi-task and manage a scientific research project, starting from the initial idea through to completion and publication in a peer-reviewed journal. etc. | 9/3/2019 |
| 14127 | Zynex Medical Englewood, CO Patient Care Representative - Call Center HS diploma, Associate degree or higher preferred Exp: Entry level |
Essential Job Duties and Reporting Responsibilities Include the Ability to: Provide Top-Notch Customer Service. Ability to work in a fast-paced, professional office environment and follow all Company policies consistently. Answer every call as quickly as possible with extreme professionalism. Meet or exceed performance standards including but not limited to answer rate, handle time, and quality. Take back-to-back phone calls from patients nationwide. etc. | 9/3/2019 |
| 14128 | Zynex Medical Englewood, CO Shipping & Warehouse Clerk HS diploma or equivalent Exp: 1-2 years |
Essential Job Duties and Responsibilities Include the Ability to: Cooperate with representatives from other departments in the organization to provide warehouse/shipping as requested. Help in shipping area to prepare shipments properly and place supplies into bags & envelopes. Monitor merchandise leaving the company warehouse, create shipping documents as needed, pull inventory from shelves for shipment, package correctly/accurately, print shipping labels, schedule pickup and ensure all shipments have proper postage. Trace and track shipments to ensure timely delivery with Endicia software. When requested, analyze shipping data to help maintain a high level of customer service. etc. | 9/3/2019 |
| 14129 | Zynex Medical Englewood, CO Shipping & Warehouse Clerk HS diploma or equivalent Exp: Entry level |
Essential Job Duties and Responsibilities Include the Ability to: Prepare & package supplies materials into envelopes for outgoing shipments to patients. Labeling packages for shipments as necessary. Assist with other areas in the warehouse as necessary. $15 per hour; Weekly overtime possible. This is an entry level position. | 9/3/2019 |
| 14130 | Zynex Medical Englewood, CO Billing Denial Analyst - Caseworker unspecified Exp: Entry level |
Essential Job Duties and Responsibilities Include the Ability to: Organize and analyze large volume of denials. Identify effective methods to appeal and fight individual denials and/or conduct bulk appeals. Perform code corrections and evaluate EOB’s when necessary. Obtain billing authorizations for the use of Durable Medical Equipment (DME) when needed. Negotiate the best pricing for Zynex for devices as well as supplies with adjustors/insurance reps as needed. Obtain information from clinics and physicians needed to provide to Insurance carriers for billing/coding support concerning devices, accessories, and supplies for recipients, insurance providers, physicians and the payer community. etc. | 9/3/2019 |
| 14131 | Zynex Medical Englewood, CO Account Representative- Health Care Administration unspecified Exp: Entry level |
Zynex is seeking the best Account Representative in the state to join our team. For more than two decades, Zynex Medical has been a leading provider of opioid free, prescription-strength pain relief. Our products are fully developed, FDA-cleared, and commercially sold. We continually strive to achieve an important mission --to improve quality of life of patients suffering from debilitating pain or illness by providing effective drug-free pain alternatives and outstanding customer care. | 9/3/2019 |
| 14132 | Wake Research Raleigh, NC Desktop Support Specialist AS/AA or equivalent Exp: 1-3 years |
RESPONSIBILITIES: Installing new computers/laptops and peripherals. Troubleshooting Windows operating systems. Configuring and or repairing existing computer setups. Perform routine desktop maintenance as well as refurbishing client equipment. Data Entry and answer calls for support as needed. Monitor and operate various computer systems in support of end users. Providing computer operations and support while working with the likelihood of frequent interruptions, multiple priorities, inquiries, etc. Troubleshoot and document applicable repair solutions for various systems. | 8/27/2019 |
| 14133 | Waters New Castle, DE Building Maintenance Technician Vocational trade school Exp: 1-3 years |
Install or repairs a variety of building systems such as HVAC, compressed air systems and plumbing systems. Will install venting, plumbing and wiring required to support the production and/or development process. Performs skilled trades work, such as carpentry or painting in the construction, repair or alteration of structures such as walls, roofs or office fixtures; uses hand and power tools as directed. Makes periodic or special inspections of the premises to determine repair work necessary; performs routine repairs and maintenance to the facility. Works from blueprints, drawings or rough sketches. Produces rough sketches of projects and assists with the development of cost estimates. etc. | 8/27/2019 |
| 14134 | Waters Golden, CO Chemistry Technician I BS/BA in chemistry or related Exp: 1-2 years |
ERA, A Waters Company, has an immediate opening for a full-time Chemistry Technician within it's Process Waters Consumables Product Line. PWC team produces TOC calibration and Quality Control standards, Conductivity and Turbidity standards, and other similar products. Responsibilities: Manufacturing, analytical verification, packaging, and labeling of all PWC products. Documentation of production and packaging. Creation of product labels and Certificates of Analysis. Inventory control of PWC products. etc. | 8/27/2019 |
| 14135 | Waters Milford, MA Software Engineer II BS in information systems, computer science, engineering, or related Exp: 1 year |
Responsible for software development, automation, and implementation within an Agile Framework. Developnew features for established product lines using C++ along with the necessary test automation using SpecFlow. Generate Root Cause Analysis to acknowledge and assess new improvementopportunities. Set and follow priorities in collaboration with PO and the immediate Agile team. Participate in regular code reviews. Eligible for Employee Referral Program. | 8/27/2019 |
| 14136 | Waters New Castle, DE Front-End Web Developer BS/BA in information sciences, graphic design, or related field Exp: 1-3 years |
TA Instruments is seeking a Digital & UI/UX Designer to join in our growing Marketing team. Typical tasks of the position include, but are not limited to: Design, implement, test, and deploy innovative new features and functionality for corporate websites and other digital media to provide an outstanding user experience. Participate in cross functional teams to conceptualize and create new digital media that drives revenue. Research emerging technologies and trends in digital and web design that fit, support, and accelerate our goals. etc. | 8/27/2019 |
| 14137 | Waters Golden, CO Chemistry Technician BS/AS in chemistry or applied science Exp: 1+ years |
Waters/ERA in Golden Colorado, is currently leading a search for a Chemistry Technician to join our company. In this role, the individual will help manufacture and package products assigned to the Waters Analytical Standards & Reagents Team. This position will work daily to meet production requirements and delivery schedules of high quality products. Responsibilities - Production: Production/manufacturing of chemical solutions to specifications – may include some analytical verification. etc. | 8/27/2019 |
| 14138 | Waters Milford, MA Concur System Support AS/AA Exp: 1+ years |
This position reports to the Concur Team Supervisor. The purpose of this role is to maintain the Global Concur Travel & Expense tool. The Concur system should reflect current Waters T&E policies and local regulatory requirements at all times and the Concur System Support is responsible for ensuring that it does. Responsibilities: Maintain the Concur system: groups, policies, roles and authorizations, negotiated rates for non-GDS suppliers. Configure Concur for changes to policies and rules. Manage data feeds to ensure: Employee data is up-to-date. etc. | 8/27/2019 |
| 14139 | Waters Milford, MA Corporate Financial Analyst II BA/BS in accounting or finance Exp: 1+ years |
Waters Corporation is seeking a Financial Analyst II to join the Corporate Accounting and Finance team. The individual will perform analytical, accounting and reporting for various corporate and division groups. Additionally, this role includes accounting and reporting responsibilities related to intercompany transactions, inventory and fixed assets. A successful candidate will need to demonstrate an ability to work and communicate well with various internal worldwide customers. etc. | 8/27/2019 |
| 14140 | Wave Life Sciences Worchester, MA Research Associate, In Vivo Biology BS/MS in biology, biochemistry, pharmacology or related Exp: 0-2 years |
WAVE Life Sciences USA seeks an experienced and highly motivated in vivo biologist. This position will primarily be based at Wave’s Worcester, MA site. This is an ideal position for an individual interested in drug discovery who would thrive in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate will be responsible for assisting in the design and execution of experiments as a member of teams focused on advancing therapeutic programs. This candidate will contribute to all levels of in vivo discovery research to support the development of nucleic acid therapies for genetic diseases. etc. | 8/27/2019 |
| 14141 | Wave Life Sciences Cambridge, MA Research Associate - Biology BS/MS in biology or related Exp: 0-3 years |
WAVE Life Sciences USA seeks a highly motivated biologist to join its research team in Boston, Massachusetts. This is an ideal position for an individual who is interested in learning cutting edge technologies and who thrives in a team-oriented, fast-paced, and crossdisciplinary biotech environment. The candidate will be responsible for designing, executing and analyzing experiments as a member of teams focused on advancing therapeutic programs and discovery research platforms. This candidate will contribute to all levels of in vitro and in vivo discovery research to support development of optimized nucleic acid therapies in multiple disease areas. Prior experience in animal handling and tissue processing are preferred, but not required. etc. | 8/27/2019 |
| 14142 | WCCT Cypress, CA Research Laboratory Technician HS diploma or equivalent Exp: 1 year |
The Research Laboratory Technician assists with the biological sampling procedures required of each clinical trial and dictates tasks to Laboratory Assistants conducting the sampling activities related to each study. This position is responsible for assisting with the coordination of the preparation, collection, documentation, processing, inventory and shipment of biological specimens for clinical trials and reports to the Laboratory Supervisor. etc. | 8/27/2019 |
| 14143 | Westat Rockville, MD Medical Records Abstractor HS diploma or equivalent Exp: 1 year |
Westat is seeking Medical Records Abstractors to work from our Rockville campus on a data collection effort to collect emergency department data from a sample of hospitals across the US. The primary role of the medical record abstractor (MRA) is to review medical records in a sampled hospital's emergency department(s), abstract specific information from the patient's chart following the project's case identification protocol, and entering the information into a data collection tool. etc. | 8/27/2019 |
| 14144 | Westat Rockville, MD Web Developer BS in computer science, information technology, or related Exp: 0-4 years |
Westat is seeking a highly motivated web application programmer/developer who will be responsible for the development and implementation of web applications to support a variety of projects across our research domains. You will join a technical community of developers and engineers providing intuitive, responsive systems to collect high quality data using various leading edge technologies and modern software development tools and platforms. etc. | 8/27/2019 |
| 14145 | Westat Rockville, MD Research Assistant BA/BS in health-related or social science field Exp: 1-3 years |
Westat is seeking a research assistant to provide patient registration support for a major National Cancer Institute contract. The primary function of this role is to set up and test patient enrollment forms in the patient registration system that enrolls patients onto oncology clinical trials. These services are provided Monday through Friday from 9:00 AM to 5:30 PM Eastern time. This position is located in our Rockville, MD office. etc. | 8/27/2019 |
| 14146 | Westat Rockville, MD Research Assistant BS/MS Exp: 1 year |
Westat has an immediate opening for a research assistant with experience in data collection procedures and materials along with a background in quantitative research and data analysis. The successful candidate will work closely with a multidisciplinary research team working on an innovative longitudinal health and aging study and a caregiving study. etc. | 8/27/2019 |
| 14147 | Worldwide Clinical Trials San Antonio, TX Nutrition Technician, PRN HS diploma or GED Exp: 6-12 months |
A PRN Research Nutrition Technician, under direct supervision, provides meals for subjects in research studies. Prepares and serves food in accordance with research specifications, and food safety standards. Maintains supplies, equipment, and records as indicated. Interacts with research subjects and medical staff. The PRN Research Nutrician Technician works under the supervision and guidance of the Research Nutrition Coordinator. He/she is not responsible for supervising other staff. etc. | 8/27/2019 |
| 14148 | Worldwide Clinical Trials unspecified, Operations Associate AS/BS Exp: 1+ years |
The Operations Associate has primary responsibility for carrying out all daily aspects of the operational work related to rater selection, rater certification/qualification, rater training content, scale acquisition, surveillance maintenance, workbook/source document, for Worldwide Clinical Trials, Inc. (WCT). The Operations Associate is responsible for ensuring all assigned projects are conducted in a timely fashion and in a manner compliant with SOPs and ICH/GCP/regulatory guidelines. The Operations Associate works under the direction of the Operations Manager, Clinical Assessment Technologies (CAT). etc. | 8/27/2019 |
| 14149 | Wright Medical San Francisco, CA Associate Sales Representative, Upper Extremities BA/BS Exp: 0-2 years |
Summary: This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This position is a field based position. etc. | 8/27/2019 |
| 14150 | Wright Medical Charlotte, NC Associate Sales Representative, Lower Extremities & Biologics BA/BS Exp: 0-2 years |
Summary: This is an entry level sales position that will require you to learn our products, market and industry. This role will support our foot & ankle and biologics portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is a field based position. etc. | 8/27/2019 |
| 14151 | Wright Medical Columbia, SC Associate Sales Representative, Lower Extremities & Biologics BA/BS Exp: 0-2 years |
Summary: This is an entry level sales position that will require you to learn our products, market and industry. This role will support our foot & ankle and biologics portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is a field based position. etc. | 8/27/2019 |
| 14152 | Wright Medical Lexington, KY Associate Sales Representative, Lower Extremities & Biologics BA/BS Exp: 0-2 years |
Summary: This is an entry level sales position that will require you to learn our products, market and industry. This role will support our foot & ankle and biologics portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is a field based position. etc. | 8/27/2019 |
| 14153 | Wright Medical Coronado, CA Sales Support Associate HS diploma/BA/BS Exp: 0-2 years |
Wright Medical is currently hiring a Sales Support Associate. The Sales Support Associate will be responsible for assisting in the successful execution of the sales plan for their assigned territory and the achievement of quarterly and annual sales plan objectives. He/she will travel within the territory and region for development & sales support. He/she will maintain open communications with their assigned leadership team and headquarter based sales training leader. He/she will perform and excel in case coverage, sales territory support functions and sales activity. He/she will achieve success with specified individual training and development plan. etc. | 8/27/2019 |
| 14154 | Wright Medical Houston, TX Associate Sales Representative, Upper Extremities BA/BS Exp: 0-2 years |
Summary: This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This position is a field based position. etc. | 8/27/2019 |
| 14155 | WuXi AppTec Marietta, GA Associate Laboratory Technician AS/BS Exp: 1 year |
Responsibilities: Levels 1 – 4 testing with proficiency. Prep carts. Performs QA / QC checklist tasks. Perform incubator checks, contract review, assist with releases. Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required. Normally receives minimal instructions on routine work and detailed instructions on new assignments. etc. | 8/27/2019 |
| 14156 | WuXi AppTec Austin, TX Clinical Project Associate HS diploma/AS Exp: 1 year |
The Clinical Project Associate I provides administrative support to clinical research projects by assisting project teams in the completion of assigned project activities. This is an in-office position with that does not require travel. Essential Job Functions: Provides operational support for Clinical Operations. Under direct supervision prepares, reviews and distributes the regulatory documentation according to Essential Regulatory Document Guidelines and Trial Master File (TMF) Plan. Under direct supervision prepares the investigator regulatory binders and other study start-up materials, following established procedures. etc. | 8/27/2019 |
| 14157 | WuXi AppTec Philadelphia, PA Associate Metrology Technician AS in a technical discipline Exp: 1 year |
Calibrates instrumentation & equipment, and documents the results consistent with all applicable quality standards according to schedule. Perform preventative maintenance, troubleshooting, and repair on instrumentation and equipment when scheduled or required. Responsibilities: Ensures that all equipment is properly calibrated and qualified according to appropriate Good Manufacturing. Practices (cGMP) and/or Good Laboratory Practices (GLP) guidelines. Provides consistent cGMP & GLP documentation practices. Communicates with supervisor and other colleagues as required. Monitors contractors for calibrations, validations, and repairs as required. etc. | 8/27/2019 |
| 14158 | WuXi AppTec Philadelphia, PA Laboratory Technician I BS in biological sciences or related Exp: 0-1 years |
Performs basic protein based assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under direct supervision, completes Test Methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs additional Research & Development activities as assigned by Management. etc. | 8/27/2019 |
| 14159 | WuXi AppTec Philadelphia, PA Laboratory Technician II BS in biological sciences or related Exp: 1-2 years |
Performs assays according to testing records and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under direct supervision, completes test methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. etc. | 8/27/2019 |
| 14160 | WuXi AppTec Philadelphia, PA Laboratory Technician I BS in biological sciences or related Exp: 1-2 years |
Performs assays according to testing records and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under supervision, completes test methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. etc. | 8/27/2019 |
| 14161 | WuXi NextCODE unspecified, Technologist I/II BS/MS in molecular biology or related Exp: 1 year |
We are seeking a highly motivated and enthusiastic Technologist I / II to develop, optimize, and perform next-generation sequencing (NGS) assays in a CLIA/CAP laboratory. ESSENTIAL FUNCTIONS: Perform laboratory functions in accordance with standard operating procedures. Extract nucleic acids from various specimens including cell lines, human blood, fresh frozen tissue and Formalin-Fixed Paraffin Embedded tumor specimens). Participate in regular Proficiency Testing. Prepare auditing documents. Collaborate with the lab manager on all activities. etc. | 8/27/2019 |
| 14162 | Xbiotech Austin, TX Cell Culture Research Associate BS/MS in cell biology, biotechnology or related Exp: 1+ years |
We are seeking a highly motivated cell culture research associate to join our Cell Line Development group in the Research and Development Department. The successful candidate will be responsible for developing and culturing CHO cell lines and will work closely with other Research and Development teams to create breakthrough antibody therapies to treat infectious diseases. etc. | 8/27/2019 |
| 14163 | Zeteo Tech Sykesville, MD Electrical Engineer BS in electrical or computer engineering or related Exp: 1+ years |
Zeteo Tech, a venture-backed company developing solution for Medical and Biodefense applications, is seeking a skilled and motivated electrical or computer engineer with and interest in embedded systems. Our ideal candidate is interested in working in an entrepreneurial environment, developing game changing solutions to healthcare and national security challenges. You'll use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. etc. | 8/27/2019 |
| 14164 | Zeteo Tech Sykesville, MD Electrical Engineer - Embedded Sensors BS in electrical or computer engineering or related Exp: 1-5 years |
Zeteo Tech, Inc, a venture backed company developing solution for Medical and Biodefense applications, is seeking a highly-skilled and motivated electrical or computer engineer with and interest in embedded systems. The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. etc. | 8/27/2019 |
| 14165 | Zeteo Tech Sykesville, MD Electrical Engineer - Software Systems BS in electrical or computer engineering or related Exp: 1-5 years |
Zeteo Tech, Inc, a venture backed company developing solution for Medical and Biodefense applications, is seeking a highly-skilled and motivated electrical or computer engineer with and interest in embedded systems. The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. etc. | 8/27/2019 |
| 14166 | zPREDICTA San Jose, CA Research Associate, Cell Biology MS in life sciences Exp: 1 year |
You will join a dynamic and agile team of scientists developing patient-derived 3D tissue culture models for cancer and immunology. You will be responsible for executing projects for our pharmaceutical clients ranging from screening of investigational compounds to exploring the mechanism of action of drug candidates. To be successful, you have to be excited by the fast-paced environment of a start-up and possess a versatile set of technical skills. etc. | 8/27/2019 |
| 14167 | Zymo Research Irvine, CA Customer Success Associate (internal sales) BS in life science Exp: 1-3 years |
The primary responsibility of the Customer Success Associate (internal sales) is to meet sales goals and generate leads by nurturing existing clients and identifying new sales opportunities. Due to the technical nature of Zymo Research products, the ideal Customer Success Associate candidate must have a life sciences background (education/work experience) to ensure engaging and productive conversations with clients. The ideal candidate should have a passion for science, sales, and customer support. Additionally, qualified candidate should enjoy being challenged and driven by achievement. etc. | 8/27/2019 |
| 14168 | Zymo Research Irvine, CA Technical Manufacturing and QC Associate BS in related, life science field Exp: |
Assist in the manufacturing of various chemicals, buffers, and other product-related components to ensure consistent product performance. Responsible for conducting quality control tests on various chemicals, buffers, and other product-related components. Essential Duties and Responsibilities: 1. Manufacturing: Assist the Technical Manufacturing Manager to manufacture chemicals, buffers, and cells for Zymo Research’s products. 2. Product Quality Control: Initiate and implement appropriate experiments according to the SOP in order to accept or reject the release of product(s) and other related product components. etc. | 8/27/2019 |
| 14169 | Vector Labs Burlingame, CA Technical Sales Representitive BS or MS Exp: 1+ years in sales |
Using NetSuite and web-based research to understand customer organizations and working with colleagues at Vector Laboratories and at each account to understand buying trends and purchasing mechanisms. Meeting and exceeding sales targets by establishing strong business relationships with current and future customers and aggressively pursuing new sales opportunities. Engaging with purchasing decision-makers at each account, establishing relationships, evaluating, prioritizing, and uncovering sales opportunities and customer concerns. | 8/26/2019 |
| 14170 | Veeva Pleasanton, CA Associate Software Engineer BS in computer sciences or related Exp: Recent Graduate |
Help us design our solutions. Contribute to technical and functional design decisions, troubleshoot and provide technical product support, and be responsible for all aspects of the software development lifecycle. Drive all aspects of the software development cycle: design, implementation, tuning, testing, and monitoring of the functional areas that you will own, delivering products within the schedules and timelines | 8/26/2019 |
| 14171 | Veeva Columbus, OH Associate Software Engineer BS in computer sciences or related Exp: Recent Graduate |
Help us design our solutions. Contribute to technical and functional design decisions, troubleshoot and provide technical product support, and be responsible for all aspects of the software development lifecycle. Drive all aspects of the software development cycle: design, implementation, tuning, testing, and monitoring of the functional areas that you will own, delivering products within the schedules and timelines | 8/26/2019 |
| 14172 | Veeva Toronto, Ca QA Engineer - Safety BS in math/computer sciences Exp: 1-4 years in QA/Development |
Veeva Systems is looking for a QA Engineer that likes to figure out how things work and make sure they are working correctly. This is a hands-on position for delivering a quality SaaS product. Create testing-related documentation, including test plans, test cases/scripts, and bug reports assessing quality and associated risk. Work closely with the automation group to automate features for better regression coverage, automate production issues, execute scripts, and triage automation runs | 8/26/2019 |
| 14173 | Veeva Pleasanton, CA Associate QA Engineer BS/BA; GPA > 3.0 Exp: Recent Graduate |
Work with product managers and developers using Agile methods to identify/refine test cases from requirements and design. Work with developers and other QA engineers in a team environment to ensure product quality. Document test cases and outcomes within a test case management application. Conduct QA tests and verify outcomes within schedules/timelines. Clearly document and explain defects found in defect tracking system. | 8/26/2019 |
| 14174 | Express Scripts Byfield, MA Data Entry Pharmacy Technician HS Diploma/GED Exp: 6 months as pharma tech |
The Front End Pharmacy Tech is responsible for performing activities under close supervision that support pharmacy management operations in the administration of pharmacy benefit for lines of business. Typically a certified pharmacy technician | 8/25/2019 |
| 14175 | Express Scripts North Burlington, NJ Warehouse Assistant HS Diploma/GED Exp: 0-1 years |
The Warehouse Assistant is responsible for performing tasks related to receiving product, stocking and replenishment, and inventory control. This includes safely unloading trucks and unpacking received product, comparing the purchase order to the product received for accuracy, counting quantities of product received and ensuring the quality of the product is at an acceptable level, and removing damaged or non-conforming product using data entry and retrieval devices to record receipt transaction (using scanners and computer input). In addition, this position safely transfers material from receiving area to warehouse or dispensing locations and ensures proper stock rotation—utilizing PDAs to update the inventory system. | 8/25/2019 |
| 14176 | United Therapeutics Research Triangle Park, NC Associate Test Engineer, Medical Device BS in engineering Exp: 0-5 years |
The Associate Test Engineer – Medical Device will manage the investigation of device product complaints. This individual will develop, document, and execute medical device test protocols; Enhance/automate test processes; Support the engineering team with testing, prototyping, and reworking activities; Responsible for equipment calibration and general lab organization. | 8/25/2019 |
| 14177 | United Therapeutics Research Triangle Park, NC Bioprocess Technician - Cell Biology AAS/BS/BA in biological sciences Exp: 1+ year in industry/cell culture |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. Routinely perform large-scale primary lung cell culture in 2D and 3D to support process development activities for a tissue engineered product. Routinely perform bioanalytical assays to phenotypically and functionally characterize cells (such as flow cytometry and plate-based assays). | 8/25/2019 |
| 14178 | United Therapeutics Silver Spring, MD Process Engineer BS in sciences Exp: 1+ years of research |
We are currently looking for a Process Engineer to join our API team. In this role, you will support the process engineering team in the specification, installation, maintenance and operation of small-molecule API production equipment and processes. Additionally, you will partner with members of the API Production and R&D team on activities as required to help internal customers efficiently produce the best medicines possible. | 8/25/2019 |
| 14179 | Unum Cambridge, MA Associate Scientist - Bioassay MS in biological sciences Exp: 1-3 years |
The primary role as an Associate Scientist will be to use and develop immunoassays and bioassays to enhance understanding of key attributes in support of cell therapy process and product development and characterization. Participate in activities to support Unum’s pipeline within established timelines and ensure data quality and integrity. | 8/25/2019 |
| 14180 | Unum Cambridge, MA Associate Scientist, Translational Medicine MS in biology, immunology or oncology Exp: 1-4 years |
Support the development, execution and analysis of assays in early clinical studies to assess ACTR T cell persistence and phenotype, target expression/occupancy, cytokine levels and immunogenicity. Explore predictive biomarkers of ACTR manufacturing and clinical success across various patient populations. Prepare data packages for technical reports, SOPs, and regulatory submissions | 8/25/2019 |
| 14181 | Vanda Pharmaceuticals West Palm Beach, FL Associate Neuroscience Specialty Sales Representative BS/BA in life sciences or business Exp: New graduate |
As an Associate Neuroscience Specialty Representative, you will be responsible for: Becoming knowledgeable of disease state, product and competitive market knowledge. Educating Healthcare providers on Vanda's product portfolio. Developing relationships with Healthcare providers in order to understand their needs. | 8/25/2019 |
| 14182 | Vanda Pharmaceuticals Dallas East, TX Associate Neuroscience Specialty Sales Representative BS/BA in life sciences or business Exp: New graduate |
As an Associate Neuroscience Specialty Representative, you will be responsible for: Becoming knowledgeable of disease state, product and competitive market knowledge. Educating Healthcare providers on Vanda's product portfolio. Developing relationships with Healthcare providers in order to understand their needs. | 8/25/2019 |
| 14183 | Vanda Pharmaceuticals Baton Rouge, LA Associate Neuroscience Specialty Sales Representative BS/BA in life sciences or business Exp: New graduate |
As an Associate Neuroscience Specialty Representative, you will be responsible for: Becoming knowledgeable of disease state, product and competitive market knowledge. Educating Healthcare providers on Vanda's product portfolio. Developing relationships with Healthcare providers in order to understand their needs. | 8/25/2019 |
| 14184 | Barry Wehmiller East Brunswick, NJ Validation Engineer (Design Group) BS in sciences/engineering/manfacturing technology Exp: 0-2 years |
The Validation Engineer will interface with our clients and be responsible for preparing and executing commissioning and qualification documents for a variety of utility, facility and process equipment. This role will include both document development and field execution of test protocols, including FATs, SATs, CTPs, IQs, OQs, PQs, PVs. Required experience with good documentation practices, cGMP, & FDA CQV methods and systems, ability to read engineering documents, set priorities, and work on multiple projects simultaneously. | 8/25/2019 |
| 14185 | Varian Palo Alto, CA HW Verification Engineer MS in engineering Exp: 1+ years |
As a Hardware Verification Engineer, you will own verification activities on new and released products. Your responsibilities will include: Collaborate with cross functional teams to ensure that Varian’s complex devices are thoroughly tested. Collaborate on requirements definition and test acceptance criteria. Develop manual and automated test methods to characterize performance of new devices from prototype to production. | 8/25/2019 |
| 14186 | Varian Palo Alto, CA Dosimetry Coordinator/Rad Safety Tech MS Exp: 0 years |
As needed for compliance with state and country regulatory requirements (North and Latin America), act as the coordinator for the Varian radiation dosimetry program that includes 1400+ permanent participants, including individuals who work at Varian sites in Palo Alto, Milpitas, and Las Vegas and Varian service personnel who receive dosimeters at individual addresses. Using Varian’s Learning Management System, ensure applicable radiation safety training requirements have been met for individuals to be added to the dosimetry program. | 8/25/2019 |
| 14187 | Varian Palo Alto, CA QA Engineer MS in related Exp: 1+ years |
We currently have an opportunity for a Quality Assurance Engineer for our Palo Alto facility. In this key role, the Quality Assurance Engineer will manage implementation, support, and maintenance of company-wide quality objectives, including analysis and trending of key quality system elements on a periodic basis. | 8/25/2019 |
| 14188 | Varian Richmond, VA Field Service Rep I HS Diploma/GED Exp: 0-1 years |
Performs client-site servicing, repair and/or installation of company product(s). This job may include any aspect of product field support, including system hardware and software, medical or laboratory devices and equipment, and systems networking. Provides technical support to customers on operational or maintenance aspects of system equipment. Serves as customer contact on technical and service related problems. Diagnoses mechanical, hardware, software and systems failures using established procedures. Determines most cost effective repair/resolution to minimize customer downtime. Prepares reports for analysis of product failure trends and service ability issues. | 8/25/2019 |
| 14189 | Upsher Smith Maple Grove, MN Corporate Sales Representative I BS in business, sciences, or communications Exp: 1-3 years in B2B |
The Corporate Sales Representative is responsible for the development and management of a designated territory with the goal of maximizing sales while improving patient lives. Patients are central to all USL strategies, and the CSR will be responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other healthcare practitioners and members of the health care community. The CSR may work in a team with a Corporate Sales Specialist (CSS), Regional Trainer, Managed Care - Regional and National Account Manager to increase sales, market share and profitability of USL products. | 8/25/2019 |
| 14190 | Teva Pharmaceuticals Salt Lake City, UT Production Support II HS Diploma/GED Exp: 1+ years |
Set up and operate packaging equipment in accordance with current good manufacturing practices and standard operating procedures. Package finished goods according to batch record format. Maintain inventory of job materials. ssue and reconcile data in the batch record required per batch. Clean production equipment or work areas. | 8/24/2019 |
| 14191 | Teva Pharmaceuticals Salt Lake City, UT Quality Control Analyst I BS in sciences Exp: 1 or more years lab experience |
Under general supervision, performs cGMP laboratory analyses of Finished products and in process materials. Performs stability testing for Finished products. Performs maintenance and calibration of analytical instruments. Operates general analytical instruments during the testing of finished products using HPLC, UPLC, GC-FID, UV-VIS, FTIR, automatic titrators, Dissolution Apparatus, particle size analyzer, Instron, Densitometer, Rheometer, viscometer (LV/RV/Cone and Plate), pH meter and analytical balance. Prepares standard, sample, and buffer solutions as required by test methods and performs all necessary calculations associated. | 8/24/2019 |
| 14192 | Teva Pharmaceuticals Salt Lake City, UT Pharmaceutical Technology Specialist I BS in sciences Exp: 1-2 years |
Under general supervision, the Pharm Tech Specialist I determines the critical aspects of manufacturing equipment with regard to product and process, and writes protocols and other records related test results. Prepares final reports that identify the results of protocol testing and the conditions of release. Assists in conducting efficiency studies and in the identification of process improvement opportunities. Participates in project coordination activities. | 8/24/2019 |
| 14193 | Teva Pharmaceuticals Salt Lake City, UT Process Operator I HS Diploma/GED Exp: 0-2 years in manufacturing |
This position is responsible for performing operations related to the manufacturing and/or packaging of drug products through equipment set-up, operation, clean-up and maintenance in compliance with all regulatory requirements and company policies and procedures. Responsible for learning the manufacturing and/or packaging process as assigned by following approved batch records (BR), work instructions (WI), standard operating procedures (SOP), etc. | 8/24/2019 |
| 14194 | TRC Columbia, SC Product Formulation Technician HS Diploma/GED Exp: 0-2 years in lab |
The Product Formulation Technician is responsible for operating compounding equipment and may be required to work in both the Commercial formulation area, as well as, the Development formulation area. Responsibilities also include following necessary methods and procedures to produce a functional compounding process. The Product Formulation Technician ensures that documentation and activities in the compounding area are compliant with any applicable regulations | 8/24/2019 |
| 14195 | TRC Columbia, SC Multi-Craft Technician 2-year technical degree Exp: 0-2 years |
Multi-Craft Technician will maintain and trouble-shoot equipment within the manufacturing department. The technician will be fully trained in the operation of all manufacturing equipment before being trained specifically on the technical maintenance and repair Standard Operating Procedures (SOP’s). Responsible for electrical and mechanical troubleshooting of fluid delivery, extrusion, hydraulic, electrical, mechanical, and conveyance systems in a clean room manufacturing environment. The technician will be required to maintain Operating Technician proficiency and in case of emergency, may be required to assist starting and ending of batch processing | 8/24/2019 |
| 14196 | West Pharmaceuticals Kinston, NC Lab Analyst BS in microbiology or sciences Exp: 1-3 years in lab |
In this role you will perform all required routine testing (Bioburden Silicone, Particle, Endotoxin) to support product release, including water testing, environmental monitoring. Support other laboratory functions as needed. Perform product release routine testing including, but not limited to, bacterial endotoxin, bioburden, particulate and silicone testing, etc. Perform routine testing to support the plant functions including but not limited to environmental monitoring in Clean Rooms, water testing etc. | 8/24/2019 |
| 14197 | West Pharmaceuticals Bangalore, IN Associate Data Scientist, D&T BS in computer/math/stats Exp: 0-3 years |
The Associate Data Scientist, Digital and Transformation will work with a multidisciplinary team to design and develop innovative data-driven analytical products and solutions for complex business problems using advanced analytics, data mining, and machine learning. Work with stakeholders throughout the organization to identify opportunities for leveraging novel statistical and machine learning techniques on data problems to solve strategic business questions. Should have a strong background and skill-sets related to programming and software development | 8/24/2019 |
| 14198 | Teravance Biopharma South San Francisco, CA Research Associate I/II BS/MS in sciences Exp: 1 or more year in drug discovery |
The successful candidate will work collaboratively with senior scientists to develop and execute pharmacodynamic and disease mechanism models designed to assess the pharmacological activity of novel molecules. Research Associate should have strong in vitro / in vivo skills. Ability to provide scientific inputs for new assay/ experimental model development. | 8/24/2019 |
| 14199 | Thermo Fisher West Hills, CA Scientist I, Manufacturing Sciences HS Diploma/GED Exp: 1-2 years lab experience |
The Scientist I, Manufacturing Sciences is responsible to manage and prioritize assigned projects related to development and improvement of DNA-based diagnostic reagents with supervision. Simultaneously manage and prioritize multiple projects and products across multiple functional groups while meeting target due dates with guidance of supervisor/lead. Design, create experimental task, run tests and be able to look at data and complete analysis using Fusion, Orchid, or equivalent software. Can provide experimental task(s) to designated Scientist with Supervisor approval. | 8/24/2019 |
| 14200 | Thermo Fisher Tewksbury, MA Manufacturing Technician HS Diploma/GED Exp: 0 years |
Component assembly with UV cured epoxy. Adhere to ISO9000 requirements including ESD, work area cleanliness, maintenance and calibration of equipment and work instruction adherence. Responsible for processing work orders for the manufacture of optical components | 8/24/2019 |
| 14201 | Thermo Fisher Tewksbury, MA Depot Repair Technician HS Diploma/GED Exp: 1-3 years |
Diagnose and repair, customer and in-process units. Keep accurate and ISO auditable records of product repairs, test results and other data as required. Adhere to ISO9000 requirements including ESD, work area cleanliness, maintenance and calibration of equipment and work instruction adherence | 8/24/2019 |
| 14202 | Thermo Fisher Florence, SC Scientist 1 BS/BA in chemistry or sciences Exp: 0-3 years |
This is an entry-level opportunity to support the Process R&D efforts at the Florence, SC facility. Conduct chemical experiments in laboratory as instructed by a senior staff supervisor. Accurately record and report experiments and scientific findings per assigned departmental standards in a timely manner to meet project objectives. Laboratory personnel will be responsible for disposing of any hazardous waste they generate in accordance with Patheon’s Hazardous Waste Training | 8/24/2019 |
| 14203 | Tolmar Windsor, CO Manufacturing Operator I HS Diploma/GED Exp: 1 or more years of experience in a GMP manufacturing environment. |
Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of "Right the First Time". Assist in the set-up of semi-automatic filling equipment used to fill dermatological products. Perform routine sampling and inspections for product attributes (fill weights, product sealing, labeling) of filled products. Perform facility cleaning of manufacturing areas as required to maintain a cGMP environment and by Tolmar Standard Operating Procedures. | 8/24/2019 |
| 14204 | Tolmar Fort Collins, CO Manufacturing Operator I HS Diploma/GED Exp: 1 or more years of experience in a GMP manufacturing environment. |
Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of "Right the First Time". Assist in the set-up of semi-automatic filling equipment used to fill dermatological products. Perform routine sampling and inspections for product attributes (fill weights, product sealing, labeling) of filled products. Perform facility cleaning of manufacturing areas as required to maintain a cGMP environment and by Tolmar Standard Operating Procedures. | 8/24/2019 |
| 14205 | Tolmar Windsor, CO Packaging Development Engineer I BS in packaging engineering or related Exp: 1 or more years in packaging |
Under general supervision, develops the packaging components and packaging requirements for existing commercial products and for development projects. Develops, maintains and monitors packaging components to ensure compliance with Quality, Safety, Manufacturing and Regulatory guidelines and procedures. Conducts testing activities that influence selection of primary, secondary and tertiary packaging components. | 8/24/2019 |
| 14206 | Texikon Bedford, MA Laboratory Assistant, In-Vivo HS Diploma/GED Exp: Entry Level |
The successful candidate will haveinteraction with In Vivo Research Associates, In Vivo Study Directors, Vet Care staff and interface with laboratory management regarding all day-to-day activities of the studies. They will be responsible for providing logistical support for the studies being conducted. As a laboratory assistant, you will be responsible for preparing animals for the studies conducted, including shaving, weighing and identification. Additionally, you will be responsible to ensure the technical conduct and regulatory compliance of your duties comply with FDA GLP and ISO regulatory guidelines. | 8/24/2019 |
| 14207 | Texikon Bedford, MA Histology Laboratory Assistant HS Diploma/GED Exp: Entry Level |
The successful candidate will have interaction with Histology Research Associates, Histology Study Directors, Vet Care staff and interface with laboratory management regarding all day-to-day activities of the studies. They will be responsible for providing logistical support for the studies being conducted. As a laboratory assistant, you will be responsible for preparing animals for the studies conducted, including shaving, weighing and identification. Additionally, you will be responsible to ensure the technical conduct and regulatory compliance of your duties comply with FDA GLP and ISO regulatory guidelines. | 8/24/2019 |
| 14208 | Tris Pharma Monmouth Junction , NJ Quality Control Chemist BS/BA in chemistry or related Exp: 1 or more years in lab |
QC Chemists perform analytical testing of raw materials, packaging component, in-process, finished product, stability samples, cleaning verification/validation, and process validation samples following Analytical Methods, Protocols, Procedures (SOP’s) and company policies. He/she follows and maintains adherence to current industry standards (cGMP’s, GLP’s, etc.) to meet production and customer demand. Qualified candidates will be expected to work either independently or as a team to achieve company goals and initiatives. | 8/24/2019 |
| 14209 | Tris Pharma Monmouth Junction , NJ Product Development/Formulation Scientist I MS in pharma sciences or related Exp: 1+ year in pharma |
Product Development R&D Scientists perform preformulation and formulation development activities, prepares formulation batches for compatibility studies, stability studies, Pilot batches and Pivotal batches, perform maintenance of Research and Development (R&D) equipment/instruments. | 8/24/2019 |
| 14210 | Endologix Santa Rosa, CA Manufacturing Engineer (Temporary) MS in engineering or sciences Exp: 1 year |
Maintain existing manufacturing processes and equipment to support output goals and product quality requirements through line support, dispositioning non-conforming material, and driving investigation and completion of CAPA. Evaluate, prioritize, and improve manufacturing processes to achieve cost of goods sold, product quality and cycle time targets. Collaborate with R&D, Quality Engineering and manufacturing team members to implement improvements. Help to design and develop manufacturing processes and tooling for new products from process conception through qualification. Collaborate with the R&D organization to help facilitate the successful execution of the New Product Development Process and launching products. | 8/24/2019 |
| 14211 | Trucode Gene Repair South San Francisco, CA Associate Scientist, Chemistry MS in chemistry Exp: 1-2 years |
We seek a highly skilled, motivated and creative chemist ready to function in a fast-paced and collaborative environment. Candidates should have exceptional solid phase peptide synthesis and/or HPLC analysis and purifications training. Successfully prepare, purify and characterize peptide nucleic acid oligomers and conjugates via solution and solid phase methodologies. Maintain the team's peptide synthesizers, HPLCs and automated synthesis workflow. | 8/24/2019 |
| 14212 | Tunnell na, PA Tech Transfer Specialist - Upstream Process MS Exp: 1+ years |
The Vaccine Process Development and Commercialization group within our client's manufacturing division focuses on late stage process development, technology transfer, and support of established vaccine products. Our client is seeking an energetic, people-oriented professional with strong scientific and technical skills to execute the tech transfer activities of multiple vaccine programs with a focus on upstream manufacturing process ( Drug Substance ). | 8/24/2019 |
| 14213 | Tedor Cumberland, RI Production Technician HS Diploma/GED Exp: 1-2 years production environemtn |
The Production Technician position performs all tasks involved in the pharmaceutical process following cGMP’s and SOP’s such as wet granulation, dry granulation, tablet compression, encapsulation, tablet coating, packaging and finished product, put product on stability. The position follows standard work methods and practices safe work habits to ensure production is as efficient and safe as possible. | 8/21/2019 |
| 14214 | Teligent Buena, NJ QC Chemist I BS in chemistry or related Exp: 0-3 years pharma/lab experience |
Provide accurate and timely testing of raw materials, finished product and/or stability samples as assigned. Ensure the safety and reliability of products produced in compliance with quality and regulatory requirements. Perform quality control testing on raw materials, finished product, pre-approval and commercial stability samples as assigned by the supervisor. Wet and Physical chemistry techniques including but not limited to: Karl Fisher, Viscosity, Microscopy, pH, specific gravity, IR, Specific Rotation and wet chemistry. | 8/21/2019 |
| 14215 | Teligent Buena, NJ 2nd Shift Compounder AA/AS Exp: 1 or more year |
Perform functions relating to the processing of Topical products (creams, ointments, lotions, solutions) ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements, and in conjunction with all Standard Operating Procedures (SOPs). Perform functions relating to the cleaning and sanitization of compounding process equipment and compounding facility to facilitate GMP compliance, quality, safety, and schedule attainment. Follow standard operating procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. | 8/21/2019 |
| 14216 | Terumo Elkton, MD Engineer I - Test and Evaluation BS in engineering Exp: 0-3 years (entry level) |
The Test & Evaluation Engineer 1 is responsible for providing engineering support for planning and execution of NPD test and evaluation activities. Testing activities may include new product concept testing, competitive benchmarking, marketing claim substantiation, formal design verification testing (including accelerated and real time aging), usability testing, and root cause analyses. The Test & Evaluation Engineer 1 may serve as an extended project team member and will typically coordinate with marketers, development engineers, process engineers, manufacturing and quality engineers. | 8/21/2019 |
| 14217 | Terumo Elkton, MD NPD Test & Evaluation Technician HS Diploma/GED Exp: 1-5 years |
The NPD Test & Evaluation Test Technician position is responsible for the preparation and testing of pre-production devices to support the product development process. The position is also responsible for testing support of competitor product evaluations for marketing information. Assisting in preparing the lab for simulated clinical evaluations and new product pilot lines is also included in the position. An additional responsibility is supporting the acquisition, calibration and validation of lab equipment. | 8/21/2019 |
| 14218 | Tempus Chicago, IL Laboratory Equipment Quality Control Technologist BS in medical technology/sciences Exp: 1 or more years in molecular lab |
Work within a cutting-edge genomics workflow to provide quality control support in a high-volume next-generation sequencing clinical laboratory. Document all results and findings in order to satisfy CLIA/CAP/NYS-DOH requirements. Report significant equipment findings/deviations and system deficiencies to lab management, as appropriate. Update SOPs and equipment records within document control system, including creation/ revision/ review of internal SOPs and other quality documentation. | 8/21/2019 |
| 14219 | Tempus Chicago, IL Jr. Clinical Trials Data Specialist BS or MS in molecular biology/genetics/biological sciences Exp: 0-2 years |
We are looking for a Jr. Clinical Trials Data Specialist who will work with our clinical and computational biology team on reports for clinical and research use. Works collaboratively within cross-functional teams at Tempus (including but not limited to scientists, pathologists, product development) to create customized clinical reports. Analyze patient clinical records and molecular testing results to identify potential clinical trials. | 8/21/2019 |
| 14220 | Talis Menlo Park, CA Research Associate MS in biological sciences Exp: 0-3 years |
The candidate will join the Assay Development group in the R&D division where focus is on molecular assays development such as nucleic acid isolation, purification, amplification and labeling technologies. Work with senior scientists and run hands-on experiments for microbiology, sample preparation, nucleic acid extraction and amplification. Be involved in reagent QC, generating and testing of designed controls and standards. | 8/20/2019 |
| 14221 | Tandem San Diego, CA Product Development Engineer I BS in mechanical/biomedical engineering Exp: 0-1 years in product development |
A team member responsible for technical contributions to the development, documentation, testing, analysis, troubleshooting, and debugging of the Company’s new medical devices, test and assembly fixtures, and data collection systems. Participates in the research and development of components and systems for the Company’s medical devices, utilizing knowledge of engineering theory and materials or component properties. Works within design controls and contributes to the design history file for medical devices by reviewing product requirements and specifications, documenting the design process, participating in formal design reviews and verifying the product performance with formal test methods, protocols and reports. | 8/20/2019 |
| 14222 | Tanvex San Diego, CA Temporary Research Associate, R&D Cell Culture BS in chemical/biomedical engineering Exp: 0-2 years in cell culture |
The Temporary Research Associate is responsible for executing individual experiments related to all aspects of cell culture process development from process definition to process characterization for support of pipeline projects. The Research Associate contributes to technology transfer from process development to clinical cGMP manufacturing and performs experiments related to mammalian cell culture development and scale up such as media selection, feed strategy development, bioreactor operations, process optimization, and metabolite analysis | 8/20/2019 |
| 14223 | Tanvex San Diego, CA Research Associate, Analytical Sciences BS or MS in chemistry/biochemistry/engineering Exp: 0-3 years |
The Research Associate will perform analytical tests using HPLC, Spectrophotometry (RP, IEX, SEC, HILIC etc.), CE, mass with high quality and efficiency; provides analytical support in R&D settings for samples from various process scales; writes experiment summaries and development reports; and assists during document review comprising of but not limited to: batch records, standard operating procedures and assay protocols. | 8/20/2019 |
| 14224 | TE Various Locations, na Product Engineering Early Career Development Program BS in mechanical/biomedical engineering Exp: Recent Graduate (August 2019-June 2020) |
Designed for graduating seniors and early career professionals, this 2-year program accelerates participant’s development by combining intensive on-the-job training, rotations across business units, locations and roles, and exposure to senior leadership. During your time this Program you may rotate into a variety of Mechanical Engineering positions throughout our organization, which may include, but is not limited to Mechanical Design Engineer, Mechanical Development Engineer, Mechanical Engineer, and Operations Rotational Engineer – Mechanical Engineering. | 8/20/2019 |
| 14225 | TE Various Locations, na Manufacturing & Process Engineering Early Career Development Program BS in mechanical/electrical engineering Exp: Recent Graduate (August 2019-June 2020) |
During your time this Program you may rotate into a variety of General Engineering positions throughout our organization, which may include, but is not limited to Manufacturing Engineering, Engineering – Stamping, Engineering Test Lab and Product Development Engineering. Designed for graduating seniors and early career professionals, this 2-year program accelerates participant’s development by combining intensive on-the-job training, rotations across business units, locations and roles, and exposure to senior leadership | 8/20/2019 |
| 14226 | TE Various Locations, na Supply Chain Early Career Development Program BS in supply/industrial engineering Exp: Recent Graduate (August 2019-June 2020) |
Designed for graduating seniors and early career professionals, this 2-year program accelerates participant’s development by combining intensive on-the-job training, rotations across business units, locations and roles, and exposure to senior leadership. Supply Chain professionals are an integral part of our organization and we are committed to hiring the right talent to grow and develop. During your time in Supply Chain Program you may rotate into a variety of Supply Chain positions throughout our organization, which may include, but is not limited to Materials Planning, Operations Associate, Supply Chain Analyst, and Supply Chain Associate. | 8/20/2019 |
| 14227 | TE Various Locations, na Electrical Engineering Early Career Development Program BS in electrical engineering Exp: Recent Graduate (August 2019-June 2020) |
Designed for graduating seniors and early career professionals, this 2-year program accelerates participant’s development by combining intensive on-the-job training, rotations across business units, locations and roles, and exposure to senior leadership. During your time in Electrical Engineering Program you may rotate into a variety of EE positions throughout our organization, which may include, but is not limited to Operations, Electrical/Plating Engineer, Electrical Testing Engineer, Electrical Component Engineer. | 8/20/2019 |
| 14228 | TE San Francisco, CA R&D/PRODUCT DVL ENGINEER I BS in electrical/computer engineering Exp: 0-1 years (recent graduate) |
The R&D/Product Development Engineering Teams provide all required product documentation including, but not limited to, Solid Model, 2D/3D production drawings, product specifications, and testing requirements. They create and modify detailed drawings and drafting or conceptual models from layouts, rough sketches or notes and contribute to design modifications to facilitate manufacturing operation or quality of product. Typical fields of expertise include: materials, mechanics and systems, electrical, optics, chemistry, software, automation systems, packaging, testing and measurement, and manufacturing of electrical, mechanical and electronic components, products, and their integration into systems. | 8/20/2019 |
| 14229 | Stryker Plainfield, IN Quality Control Technician HS Diploma/GED Exp: 1-2 years in quality control inspection |
Under general supervision, performs routine to moderately complex and repetitive inspection tasks using standard procedure, gauges, tools, and equipment. Will perform incoming inspection on components and Electro/mechanical products per company/regulatory specifications. Will work from engineering schematics or blueprints to perform accurate checks and tests. Will be required to comply with documentation and regulatory procedures and policies. | 8/19/2019 |
| 14230 | Sun Pharma Billerica, MA QC Microbiologist I BS in biology/microbiology Exp: 1+ year working in lab |
The QC Microbiologist performs GMP testing of raw materials, in-process and finished products, stability samples, and non-routine sample analyses per established procedures and methodology. Record GMP data, monitors and evaluates QC systems and equipment. Interact with internal and external auditors including government agencies and contract manufacturing representatives. | 8/19/2019 |
| 14231 | Sword Diagnostics Chicago, IL Research AssociateI, Product Applications BS/BA in biological/chemical sciences Exp: 1-3 years |
Your main responsibilities will be to perform functions in support of Product Application Scientist(s) and other individuals as needed, perform common laboratory testing (including ELISA) using established protocols, prepare buffers and other chemical solutions as needed and use proper personal protective equipment (PPE) and good aseptic technique to handle biological (including human) samples. On a day-to-day basis, you will be expected tosuggest, plan and carry out studies with guidance of supervisor, record data for evaluation, analyze results with guidance of supervisor and assist other lab personnel as needed, maintain organized records of studies performed, and other duties and responsibilities as assigned. | 8/19/2019 |
| 14232 | Syneos Health Miami, FL Research Assistant I (Per Diem) BS/BA in life sciences Exp: 0-1 years work experience |
Ensure the well-being of volunteers and that adverse events are gathered and documented. * Perform the full spectrum of technical activities related to the field of expertise. * Perform catheter insertion and venipuncture. * Measure vital signs within the required timeframes. * Performs intradermal, intracutaneous and intramuscular injections. * May be called upon to insert nasogastric tubes and to perform any other tasks for projects. * Prepare, collect and process pharmacokinetic and pharmacodynamic samples. * Measure physiological data (weight, height, bone structure). * Perform electrocardiograms. * Collect and process diagnostic samples (alcohol breath tests, urine samples). * Ensure that the informed consent form is read, details study specifics, and answers volunteer questions. | 8/19/2019 |
| 14233 | Synthego Redwood City, CA Research Associate - Pre Clinical BS in biological sciences Exp: 1 or more year in bio lab |
Research Assistant - Pre-clinical will be trained to provide technical support to the senior scientist on a defined project from conception to proof-of-concept in vitro and in vivo. Process leukopacks and bone marrow to isolate primary cell culture (ie - stem cells and T cells) depending on the project. Maintain and expand primary cells. Test conditions to optimize gene editing of specific cell type | 8/19/2019 |
| 14234 | Synthego Redwood City, CA Laboratory Associate, CRISPRevolution AA in chemistry/biotechnology Exp: 1-3 years in industry |
As a Lab Associate at Synthego, you will join our growing operations team and have direct responsibility for the synthesis and purification of our gRNA products. This role requires a strong attention to detail, a desire to learn and adapt to new processes, and familiarity with safe laboratory practices. This role will combine hands-on laboratory protocols with advanced automation to ensure the timely delivery of high quality products to our customers. | 8/19/2019 |
| 14235 | Alexion Bogart, GA PPU Technician HS Diploma/GED Exp: 1+ years with lab animals |
The Protein Production Unit Technician (PPU Technician) will provide daily care and health monitoring of animals; follow standard operating procedures and good documentation practices; organize, clean, and maintain production rooms, supplies, and equipment for egg layers. The PPU Technician will support the production facility by working shifts, weekends, and holidays as needed. | 8/19/2019 |
| 14236 | SBI Palo Alto, CA Customer & Technical Support Representative BS in life sciences Exp: 1-2 years |
SBI seeks to hire a customer and technical support representative. The ideal candidate will have a B.S. degree in the life sciences and will support an existing group of customer support personnel taking telephone orders from customers, logging into a CRM system, printing packing slips, sales orders, and shipping documentation, and assist with packaging of life science reagents for shipment to worldwide customers. This position will also provide support to the Commercial Team. | 8/19/2019 |
| 14237 | System1 Biosciences San Francisco, CA Research Associate BS or MS in biological sciences Exp: 1 or mor years with tissure culture |
You’ll work with a team of scientists and engineers on these responsibilities and more: Culturing iPSCs. Differentiating iPSCs into neurons. Imaging cells using fluorescent imaging systems. Manipulating cells via transfections, dyes, or viruses. Troubleshooting experiments | 8/19/2019 |
| 14238 | Takeda Round Lake, IL Production Associate AA/AS Exp: 0-2 years manufacturing |
The Production Associate (PA) is responsible for executing all processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, responsible for the hands-on execution of all activities in the production area | 8/19/2019 |
| 14239 | Takeda Round Lake, IL Production Associate AA/AS Exp: 0-2 years manufacturing |
The Production Associate (“PA”) is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. The PA is expected to fully participate in both departmental projects and any quality working teams which may be applicable. Under the general direction of the lead technician and the overall direction of the supervisor, this position is responsible for the hands-on execution of all activities in the production area. | 8/19/2019 |
| 14240 | Takeda Social Circle, GA Lab Technician BS/BA in biomedical discipline Exp: 1 or more year lab experience |
The Lab Testing Technician is responsible for performing testing in accordance with established Standard Operating Procedures (SOPs), applicable sections of the Code of Federal Regulations (CFRs), with emphasis on Good Manufacturing Practices (GMPs), the Clinical Laboratory Improvement Act of 1988 (CLIA), and applicable Takeda and BioLife policies, procedures and quality initiatives. Perform only high and moderate complexity tests for which certification has been authorized by the laboratory director or designee and deemed commensurate with their education, training, and technical abilities. | 8/19/2019 |
| 14241 | Veeva Columbus, OH Associate, Sales Support BS/BA Exp: 0-2 years |
We are looking for a Sales Support associate to join our team. You will be a partner to the Sales team and manage the operational steps required to effectively engage, retain and support our existing customers ongoing needs related to their Veeva software subscriptions. Our ideal candidate is a motivated, goal oriented, recent college graduate who is interested in developing sales support and customer service best practices. We expect you to perform well in a team environment and have exceptional communication skills. Ultimately, you should be able to create and maintain good customer relationships and help support sales team operations. etc. | 8/19/2019 |
| 14242 | Veeva Pleasanton, CA Associate Technical Writer BA in English, communications or similar Exp: 0-2 years |
Vault Clinical Data Management Systems (CDMS) is looking for an excellent technical writer who can write high-quality, usable documentation that enables our customers to use our applications successfully. If you enjoy solving puzzles and presenting complex, technical information into comprehensive, well-organized, and easy-to-understand documentation, this is the job for you! The Associate Technical Writer is expected to be located in headquarters at our Pleasanton office. This position is not available remote. | 8/19/2019 |
| 14243 | Veracyte South San Francisco, CA Lab Assistant - Accessioner AS/BS in a life science Exp: 1 year |
Due to the success of our genomic tests and our product pipeline, Veracyte is hiring an additional team member for our CLIA Molecular Lab. The Lab Assistant - Accessioner will perform routine specimen accessioning in accordance with established protocols. The position will process specimens upon receipt in the lab. Additional responsibilities include all related clerical functions, lab maintenance and regulatory compliance tasks. You'll work alongside a highly engaged team of Lab Assistants and Clinical Lab Scientists and will collaborate with other groups across Veracyte. You'll have the opportunity for ongoing training, competency assessments and sharing ideas for continuous improvement in the lab. The work schedule is Tuesday - Saturday. etc. | 8/19/2019 |
| 14244 | Verge Genomics South San Francisco, CA In Vivo Research Associate BS in biology, neuroscience, or related Exp: 1+ years |
Do you want to be a part of a dynamic group that tests and validates novel compounds in preclinical model systems? In this position, you will support our entire in vivo team by performing efficacy, PK, and other experiments. In addition to rodent work, part of this position will require coordinating and managing samples at contract research organizations (CROs). In our newly-built South SF laboratory, you will help our in vivo team discover novel targets in neurodegenerative diseases. We are looking for detail-oriented and self-motivated individuals who are looking to make a difference in patients’ lives. etc. | 8/19/2019 |
| 14245 | Verge Genomics South San Francisco, CA Molecular Biology Research Associate MS in molecular biology, neuroscience or related Exp: 1+ years |
Verge Genomics is seeking a motivated and diligent Molecular Biology Research Associate/ Sr. Research Associate with experience in next-generation sequencing (NGS), specifically RNA extraction and library prep. In this position, you will work across all functions of Verge, including the in-vitro, in-vivo and computational biology teams. In addition to bringing library preparations in house at Verge, you will be responsible for working with human post-mortem brain and preclinical samples to generate data used to identify new potential therapies in neurodegeneration. etc. | 8/19/2019 |
| 14246 | Vericel Cambridge, MA QC Analyst I BA/BS Exp: 1 year |
Perform microbiological assays for in-process and final product samples. Perform analytical methods for final bulk material/finished goods. Test and disposition of raw materials and perform environmental monitoring. Review of QC data for compliance to procedures and specifications. Calculate and evaluate results. Participate in lab maintenance and administration duties. etc. | 8/19/2019 |
| 14247 | Veristat Etobicoke, ON Network Support Associate AS/BS in computer science, engineering, or math Exp: 1-3 years |
The Network Support Associate is responsible for user and desktop support (hardware and software), computer repair, helpdesk, and application support. S/he performs a variety of information technology support duties to ensure smooth delivery of technology services throughout the organization, providing consistently high service levels to internal customers. As a Network Support Associate You Will… Install, monitor, operate, coordinate, assist, and train others in the operation of computer hardware, software, and peripherals to meet customer needs. Utilize computer equipment, software, and diagnostic tools to perform a broad range of customer assistance, equipment maintenance, and repair assignments. Exercise judgment and creativity in selecting and applying procedures correctly, and determines when to escalate issues to the next level of support. etc. | 8/19/2019 |
| 14248 | Vertex Boston, MA Temporary Scientific Associate II BS/MS in a related field Exp: 0-2+ years |
Vertex is seeking a talented individual to join our Formulation Development group in Boston, MA. Formulation Development group is a fast paced and high energy environment. The ideal candidate has mastered the fundamentals of chemistry and physics and has direct experience in a research laboratory (e.g., has completed a cooperative training program, a summer internship, or undergraduate research). The candidate must comfortably take the initiative, be curious, and show resilience in solving complex problems. etc. | 8/19/2019 |
| 14249 | Vertex Boston, MA Administrative Assistant, Corporate Communications BA/BS Exp: 1-3 years |
Vertex Pharmaceuticals is looking for an Administrative Assistant to support the Corporate Communications and Corporate Social Responsibility (CSR) team in Boston, MA. This position is responsible for performing a variety of administrative duties across the Corporate Communications team. The Administrative Assistant must have proven experience in building collaborative relationships among his/her superiors, peers and subordinates. The ability to embrace and enhance Vertex’s culture is paramount to success in this role. The candidate must have strong achievement drive, with an impeccable work ethic, able to provide full support to enable the team to maximize their productivity and time. The Administrative Assistant plays an important role in ensuring the effective and efficient maintenance of departmental processes, procedures and programs inclusive of travel arrangements, calendar management, scheduling, Purchase Orders, vendor meetings and expenses. etc. | 8/19/2019 |
| 14250 | ViaCord (PerkinElmer) Waltham, MA Associate Scientific Services Specialist, Lab Technician AS in life sciences Exp: 1-2 years |
The candidate will conduct laboratory maintenance procedures in compliance with established protocols and in compliance with regulatory and laboratory requirements. He or she will work closely with other functional teams, providing critical lab support within the cell culture laboratory environment. Maintains suite equipment including, but not limited to: incubators, water baths, and biosafety cabinets. Monitors incubator temperature, CO2 and humidity. Responsible for the cleaning, sterilization and equipment functionality. Collaborate with Scientific Service and Asset Management teams on-site to coordinate any service-related issues. Maintains logs and accurate record keeping of worked performed. Develops and innovates continuous improvement, may collaborate with PerkinElmer technology services to implement new solutions. | 8/19/2019 |
| 14251 | ViaCord (PerkinElmer) Austin, TX Associate Scientist BS/BA in relevant life sciences Exp: 1+ years |
Perform lab experiments as planned and document all observations and findings. Prepare hybridization capture NGS libraries and amplicon panel NGS libraries. Analyze and interpret data. Present experimental findings and interpretations to senior research team members. Demonstrate potential for technical proficiency and ability to collaborate with others. Participate with other R&D team members in troubleshooting and identifying new opportunities for optimization, applications, or products. | 8/19/2019 |
| 14252 | ViaCord (PerkinElmer) Austin, TX Associate Scientist BS/BA in relevant life sciences Exp: 1+ years |
Perform lab experiments as planned and document all observations and findings. Prepare hybridization capture NGS libraries and amplicon panel NGS libraries. Analyze and interpret data. Present experimental findings and interpretations to senior research team members. Demonstrate potential for technical proficiency and ability to collaborate with others. Participate with other R&D team members in troubleshooting and identifying new opportunities for optimization, applications, or products. | 8/19/2019 |
| 14253 | ViaCyte San Diego, CA Manufacturing Associate BS in biological or engineering science Exp: 1+ years |
As a member of the Cell Manufacturing/Combination Product team, incumbent will perform a broad range of tasks in the cGMP manufacture of cells and combination cell therapy/device products for use in clinical and developmental studies. This position includes hands-on participation including materials logistics, assisting in manufacturing operations, and may include non-routine development activities. This is a full time position. etc. | 8/19/2019 |
| 14254 | Vicarious Surgical unspecified, Manufacturing Operations Engineer AS in mechanical engineering technology Exp: 1-4 years |
As the Manufacturing Operations Engineer, you will wear many hats in supporting a fast-growing robotic surgical company. This role will coordinate with multiple internal departments to set-up best practices in operations, manufacturing, inventory control, inspection, and material flow. As we expand into new space, you will be tasked with everything from production floor set-up to strategic development of layout and processes. To succeed in this role, you will need to be a good communicator with a strong sense of urgency, flexibility, and a self-starter attitude. This role reports directly to the Vice President of Operations. etc. | 8/19/2019 |
| 14255 | Vigene Biosciences Rockville, MD Fill/Finish Manufacturing Associate – Level II BS in science or engineering Exp: 1-3 years |
The Upstream Manufacturing Associate applies a broad knowledge of biological, bioprocess, and mechanical principles to execute complex operations that result in clinical and commercial stage medicines to dramatically improve the human condition through gene therapy. We believe this path may lead to real cures. You could be part of what many thought was not possible! Responsibilities: Perform basic to complex activities in dispensing of Drug Substance and final fill-finish of Drug Product using SOPs and Batch Production Records. Performing critical downstream activities in preparation of fill finish of Drug Product. Document all activities in Batch Records, Logbooks, Forms, etc. | 8/19/2019 |
| 14256 | Vigene Biosciences Rockville, MD Downstream Manufacturing Associate – Level II BS in science or engineering Exp: 1-3 years |
The Upstream Manufacturing Associate applies a broad knowledge of biological, bioprocess, and mechanical principles to execute complex operations that result in clinical and commercial stage medicines to dramatically improve the human condition through gene therapy. We believe this path may lead to real cures. You could be part of what many thought was not possible! Responsibilities: Perform downstream purification activities such as Chromatography, TFF, Ultracentrifugation, and Final Formulation steps. Perform various filter integrity tests throughout the process. Document all activities in Batch Records, Logbooks, Forms, etc. | 8/19/2019 |
| 14257 | Vigene Biosciences Rockville, MD Upstream Manufacturing Associate – Level II BS in science or engineering Exp: 1-3 years |
The Upstream Manufacturing Associate applies a broad knowledge of biological, bioprocess, and mechanical principles to execute complex operations that result in clinical and commercial stage medicines to dramatically improve the human condition through gene therapy. We believe this path may lead to real cures. You could be part of what many thought was not possible! Responsibilities: Perform basic to complex activities in seed train, bioreactor, transfection and recovery operations for both suspension and adherent cultures using SOPs and Batch Production Records. Document of all activities in Batch Records, Logbooks, Forms, Etc. Document all activities in Batch Records, Logbooks, Forms, etc. | 8/19/2019 |
| 14258 | Vigene Biosciences Rockville, MD Scientist/Engineer – Upstream Process Development MS in chemical engineering, bioengineering, cell biology, or related Exp: 0-3 years |
As a part of the Upstream Process Development team, the Scientist/Engineer is responsible for working with clients to evaluate upstream processes and ensure proper technology transfer from clients. In addition, the Scientist/Engineer will develop robust seed train and bioreactor processes and scale-up upstream processes to ensure successful transfer to cGMP manufacturing. Responsibilities: Working with clients in evaluation of upstream processes, sourcing reagents, equipment, and materials for specific projects and ensuring proper technology transfer from client. Process demonstration using bench-top bioreactors. Development of optimized, characterized, and robust seed train and bioreactor processes. etc. | 8/19/2019 |
| 14259 | Vigene Biosciences Rockville, MD Research Associate BS in chemical engineering, bioengineering, cell biology, or related Exp: 0-3 years |
As a part of the Upstream Process Development Team, the Research Associate is responsible for working with clients in evaluation of upstream processes, sourcing reagents, equipment, and materials for specific projects. Responsibilities: Working with clients in evaluation of upstream processes, sourcing reagents, equipment, and materials for specific projects and ensuring proper technology transfer from client. Process demonstration using bench-top bioreactors. Development of optimized, characterized, and robust seed train and bioreactor processes. Scaling-up of upstream processes to ensure successful transfer to cGMP manufacturing. | 8/19/2019 |
| 14260 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. Accept or reject test results in accordance with standard operating procedures. etc. | 8/19/2019 |
| 14261 | Viracor Lee's Summit, MO Laboratory Data Entry Quality Control Review I HS diploma or equivalent Exp: 1 year |
The Laboratory Data Entry QC Review associate is primarily responsible for the review and audit of order entry information and performing duties with a high degree of proficiency. Employee Responsibilities: Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other test ordering systems. Ability to prioritize and organize efficient work flow, demonstrating excellent time management skills. Ability to maintain detailed and accurate records with great attention to detail, according to good documentation practices. Make appropriate internal or external contact to resolve patient demographic issues or discrepancies. Complete correction requests as needed in a timely manner. etc. | 8/19/2019 |
| 14262 | Viracor Lee's Summit, MO Laboratory Specimen Processor I HS diploma or equivalent Exp: 1 year |
This is a Part Time position. Schedule is Tuesday – Saturday, 9:00AM – 2:30PM, with overtime as needed. Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other specimen tracking system. Examine samples for accuracy and other requirements (sample type, stability, volume, etc.). Label samples for delivery to proper area(s). Use and maintain applicable sample storage materials (i.e. dry ice). Make appropriate internal or external contact to resolve patient demographic issues or discrepancies. Complete correction requests as needed. Adhere to all Data Management policies and protocols. etc. | 8/19/2019 |
| 14263 | Viracor Lee's Summit, MO Laboratory Specimen Processor I HS diploma or equivalent Exp: 1 year |
This is a Full Time position. Schedule is Tuesday – Saturday, 8:30 A.M. – 5:00 P.M., with overtime as needed. Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other specimen tracking system. Examine samples for accuracy and other requirements (sample type, stability, volume, etc.). Label samples for delivery to proper area(s). Use and maintain applicable sample storage materials (i.e. dry ice). Make appropriate internal or external contact to resolve patient demographic issues or discrepancies. Complete correction requests as needed. Adhere to all Data Management policies and protocols. etc. | 8/19/2019 |
| 14264 | Viracor Lee's Summit, MO Laboratory Specimen Processor I HS diploma or equivalent Exp: 1 year |
This is a Full Time position. Schedule is Monday - Friday, 11:00 P.M. – 7:30 A.M., with overtime as needed. Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other specimen tracking system. Examine samples for accuracy and other requirements (sample type, stability, volume, etc.). Label samples for delivery to proper area(s). Use and maintain applicable sample storage materials (i.e. dry ice). Make appropriate internal or external contact to resolve patient demographic issues or discrepancies. Complete correction requests as needed. Adhere to all Data Management policies and protocols. etc. | 8/19/2019 |
| 14265 | Viracor Lee's Summit, MO Research Scientist I BA/BS Exp: 0-3 years |
The Research Scientist is primarily responsible for conducting research, development, validation and execution of assays to meet the development requirements within corporate/client timelines and cost objectives. Learn new techniques and instrumentation. Implement research plans, designs and testing protocols. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Keep accurate documentation of all research project steps according to Viracor Eurofins regulatory guidelines. Complete scientific write-ups of results and methods of performed experiments. Accurately prepare, label and store reagents, standards, controls, proficiency testing material and patient specimens for analytical, clinical and biopharma validations analysis and short and long-term storage. etc. | 8/19/2019 |
| 14266 | Virbac St. Louis, MO Pharmaceutical Operator - Level 1 HS diploma or equivalent Exp: 1-3 years |
Operate filling and packaging production unit for FDA and EPA regulated and less regulated pharmaceutical products. Operate equipment - Main activities: Organize their activity for production processes. Perform equipment set-ups and make adjustments. Perform line clearances. Perform unit and equipment cleaning procedures. Monitor key line parameters. etc. | 8/19/2019 |
| 14267 | Voyager Therapeutics Cambridge, MA Research Associate, Biology BS/MS in biology or related Exp: 1-3 years |
We are seeking an experienced and highly motivated biologist to contribute to our biochemical and molecular biology research team at our facility in Cambridge, Massachusetts. This is an ideal position for an individual with a background in molecular and cellular methods, who thrives in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. The individual will work at the bench on multiple projects and be responsible for experimental execution and data analysis for research studies supporting therapeutic programs and platform discovery research. We are looking for prior hands-on experience with techniques such as DNA/RNA isolation from tissue, RT-qPCR, ddPCR, Western blot, and ELISA. | 8/19/2019 |
| 14268 | Voyager Therapeutics Cambridge, MA Research Associate / Senior Research Associate, Histology BS in neuroscience, biology, or related Exp: 0-2 years |
Voyager Therapeutics seeks an entry level and highly motivated biologist to contribute to its research team at its facility in Cambridge, Massachusetts. This is a hands-on position for a person committed to helping the group conduct innovative drug discovery research while meeting deadlines and company goals. We are seeking a person who is enthusiastic about biomedical research and can work collaboratively with other scientists and team members. This is an ideal position for an individual strong experience in histological techniques such as tissue processing, sectioning, special staining, and immunohistochemistry methods and laser capture microdissection. The successful candidate should thrive in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment. This position reports in directly to the Scientist II, Neuroscience. etc. | 8/19/2019 |
| 14269 | Voyager Therapeutics Cambridge, MA Research Associate/Senior Research Associate, AAV Capsid Discovery BS/MS Exp: 0-3 years |
Voyager Therapeutics seeks a highly motivated and experienced molecular biologist to contribute to its research team at its facility in Cambridge, Massachusetts. The candidate will be involved in novel AAV capsid discovery, screening AAV variant libraries in small and large animals and engineering capsids for desired properties. This is an ideal position for an individual with extensive hands-on cellular and molecular expertise, who has a can-do attitude and strong work ethic, and thrives in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment. This position reports into the Scientist II, Vector Engineering. | 8/19/2019 |
| 14270 | Voyager Therapeutics Cambridge, MA Research Associate Scientist I/II, Upstream Focus MS in biological science or chemical engineering Exp: 1-2 years |
This senior research associate scientist will contribute hands-on to manufacturing and QC of diverse, in-house research-grade rAAV vectors for in vitro and in vivo research studies. In this role, the individual will participate in upstream and downstream processing of small- to medium-scale research-grade batches of rAAV vectors using multiple production systems. Since multiple novel AAV capsids will be evaluated, development of new production methods will be a key component of the work with a focus on purification development. This individual will play an important role assisting the head of the group in prioritizing and planning the vector production work and implementing process improvements. The main focus for this role is upstream technology development and management of all cell culture demands. etc. | 8/19/2019 |
| 14271 | Vyaire Medical Irvine, CA Quality Design Assurance Engineer BS in science or related Exp: 1-3 years |
As a Design Assurance Engineer you will review test plans and protocols, Design History files, ISO13485 requirements and CFR820 design control requirements to ensure that medical device/equipment products meet all quality standards. Oversee product quality throughout the entire product design realization process. Work closely with research and development to support new product development and improve product design. Remediate legacy design files, risk files and DHF’s and develop a harmonized DHF system for new and legacy products for Vyaire. This position will primarily focus on DHF remediation in complying with the new European standards to comply with MDR.Work under general supervision with latitude for independent judgment. Required to consult with senior peers on certain projects as required. etc. | 8/19/2019 |
| 14272 | Stryker Leesburg, VA Fulfillment Technician I HS Diploma/GED Exp: 0-1 year related experience |
Ensures complete fulfillment of all replenishment orders. Unloads daily shipment of incoming surgical sets and does the precautionary cleaning of incoming sets. Verifies kind and count of replenishments prior to shipping. Processes and stages outgoing replenishments. Performs the last check of replenishments and surgical sets prior to final boxing for shipment | 8/19/2019 |
| 14273 | Stryker Leesburg, VA Product Inspector HS Diploma/GED Exp: 0-1 year related experience |
Processes surgical sets to fulfill daily set orders and assists with other responsibilities held by Stryker Loaner Operations team. Develops an understanding of all Stryker product offerings through the repetition of processing loaner sets, beginning with small less complex sets then working up to larger sets containing both implants and instrumentations. Performs initial quality checks on instrumentation ranging from simple visual examinations to more complex functional checks | 8/19/2019 |
| 14274 | Veristat Morrisville, NC Biostatiscian MS in statistics, biostatistics, or related Exp: 1 year |
Provides statistical input into protocol and case report form (CRF) development in all therapeutic areas (e.g., trial design, sample size estimation, randomization, statistical methods for protocols, edit checks for clinical trial data). Communicates with clients regarding study protocol or statistical analysis issues. Writes detailed statistical analysis plans including specifications for analysis files, consistency checks, tables, and figures. Analyzes clinical trial data producing accurate results representing the outcome of the trial. Validates statistical output. Accurately interprets statistical results and concepts. With the medical writer, co-authors final integrated reports of clinical trial data by writing thorough and clear statistical methods sections and producing the statistical appendix for the final report. etc. | 8/19/2019 |
| 14275 | Viant Indianapolis, IN Design Engineering BS in engineering Exp: 1+ years |
Initiates, directs and manages the design, development, constructing and modification of products and processes from conception to implementation. Works closely with other departments and customers to coordinate design engineering activities. Reviews, initiates or approves engineering drawings, layouts, changes orders and specifications. SPECIALIZED SKILLS AND KNOWLEDGE: Strong CAD background required; Solidworks preferred. Sheet metal experience preferred. Strong written and oral communication skills required. etc. | 8/19/2019 |
| 14276 | Viant San Antonio, TX Assembler 1st Shift HS diploma or equivalent Exp: 0-4 years |
This position has the authority to stop production at his/her work station when there is question or concern about the acceptability of materials, subassemblies, assemblies and processes that affect the quality and safety of Viant products. ESSENTIAL JOB FUNCTIONS: Performs assembly per approved documentation and training. Performs equipment set-ups. Inspects product and paperwork for compliance to production standards. Identifies areas for process improvement and makes recommendations to supervision. Reviews documentation for completeness and accuracy. Maintains high standards in quality and throughput. Applies common sense understanding to carry out detailed written and oral instructions. Demonstrates understanding of the product and process flow for assigned work area. etc. | 8/19/2019 |
| 14277 | Viant San Antonio, TX Assembler 2nd Shift HS diploma or equivalent Exp: 0-4 years |
This position has the authority to stop production at his/her work station when there is question or concern about the acceptability of materials, subassemblies, assemblies and processes that affect the quality and safety of Viant products. ESSENTIAL JOB FUNCTIONS: Performs assembly per approved documentation and training. Performs equipment set-ups. Inspects product and paperwork for compliance to production standards. Identifies areas for process improvement and makes recommendations to supervision. Reviews documentation for completeness and accuracy. Maintains high standards in quality and throughput. Applies common sense understanding to carry out detailed written and oral instructions. Demonstrates understanding of the product and process flow for assigned work area. etc. | 8/19/2019 |
| 14278 | SRI International Menlo Park, CA Bioscience Research Associate I BS in biological sciences Exp: 1 year experience |
Research involves use of physiological data acquisition systems including measurement of EEG, EMG, body temperature and locomotor activity. Must be able to carefully follow established research protocols and to reliably make solutions following written recipes. Ability to research scientific literature to help interpret experimental results and to suggest modifications of experimental procedures is important. Good record keeping and data management are essential. | 8/18/2019 |
| 14279 | SRI International Menlo Park, CA Education Research Assistant - Center for Learning & Development BS in child development/education/psychology/related Exp: 1-2 years in education/child development |
We are seeking to hire an entry level Research Assistant in the Center for Learning and Development (CLD), at SRI International. CLD conducts a variety of research, evaluation, and technical assistance projects involving state agencies, children, families, social service programs, teachers, communities, and schools. Key areas of focus include early childhood (EC), early intervention/early childhood special education, K-12 education, behavioral health, and children and youth with disabilities. The position offers opportunities for professional growth and promotion commensurate with the research assistant’s skills and performance. | 8/18/2019 |
| 14280 | SRI International Princeton, NJ Mechanical Engineer BS in mechanical/aerospace engineering Exp: 0-2 years |
Based in Princeton, NJ, the candidate would join a multidisciplinary group dedicated to the development of custom image sensor devices, modules, and systems for numerous commercial, spacecraft, and government applications. Design mechanical parts, and assemblies using SolidWorks. Verify designs using SolidWorks Simulation and SolidWorks Simulation Professional. | 8/18/2019 |
| 14281 | Starkey Hearing Technologies Eden Prairie, MN Research Audiologist I MS in audiology Exp: 1 year or more |
We are looking for a Research Audiologist that will be responsible for research, subject and data management related to activities pertaining to Alpha and Beta product evaluations, pilot testing, and hearing aid fitting methods. This position will assist in determining the direction of product development. Work will be collaborative with other researchers and personnel in Minnesota. | 8/18/2019 |
| 14282 | Starkey Hearing Technologies Eden Prairie, MN Systems Verification Engineer II BS or MS in electrical engineering or related Exp: BS: 1 year, MS: 0 years |
The Systems Verification Engineer I & II will contribute in defining, documenting, performing, and analyzing verification tests for hearing aids, accessories, manufacturing software, fitting software, mobile applications, programmers, their components and sub-systems. The responsibilities of the Systems Verification Engineer I & II may include the automation of product system verification tests which require additional software engineering capabilities and experience. S/He must have the ability to work both independently and in a group environment. | 8/18/2019 |
| 14283 | Starkey Hearing Technologies Eden Prairie, MN Regulatory Affairs Specialist II BS/BA in science or engineering Exp: 1 or more years in related field |
This position will work with various departments across the organization such as Sales and Marketing to the Product Development group with guidance from senior regulatory personnel throughout the product life cycle. You would support activities that keeps Starkey current with changes to medical device regulations. This position is also responsible for creating and maintaining the technical files for all medical devices and hearing related products. | 8/18/2019 |
| 14284 | Stereotaxis St. Louis, MO Marketing Associate BS/BA in marketing, business admin, engineering or related Exp: 1-2 years in medical devices |
The Marketing Associate has marketing responsibility to support company-wide processes and to help drive market-competitive initiatives. The Marketing Associate will be a key member of the marketing team and will frequently interact with senior leaders in the company. Support preparation and execution for industry conferences and other events. Events include booth display, live procedure transmissions, and symposiums. | 8/18/2019 |
| 14285 | Stereotaxis St. Louis, MO Field Service Engineer AS/AA in electronics Exp: 1-5 years field service experience |
Provide on site and remote service and support of Stereotaxis magnetic navigation systems including permanent magnets, and servo control systems. Interface with customers and vendors to ensure a quality service experience and that all expectations are met. | 8/18/2019 |
| 14286 | Steris Chicago, IL Sterile Processing Technician HS Diploma/GED Exp: 0-1 years SPD experience |
Provides on-site support for the reprocessing of surgical instruments and trays to contracted facilities in compliance with the Department of Health, TJC, OSHA, CDC, AAMI and AORN standards and facilities goals and policies. Position level will be determined by previous job related experience, performance and certification requirements. | 8/18/2019 |
| 14287 | Steris Little Rock , AR Repair Technician HS Diploma/GED Exp: No experience required |
The primary role of the Repair Technician is to perform repairs on medical instrumentation. Technicians will be trained to become familiar with various types of surgical instruments and understand how to best maintain and repair them. Repairs are completed on a repair truck onsite at a hospital or surgery center. In addition to repair work, Technicians may work with a team including Sales Representatives and RCs (Repair Consultants/Managers) to identify and capitalize on revenue opportunities. | 8/18/2019 |
| 14288 | Steris Northborough, MA Validation Technician BS/BA in science or engineering Exp: 1 or more year in sterilization |
The Validation Technician assists in the processing of Customer products, and coordinates production scheduling, validations and qualifications. Contributes to the accurate and safe processing capability of the company by coordinating and scheduling all Customer validations and dose mappings; calibrates and maintains proper function of data collection devices used in validations and qualifications; investigates analyzing and reporting procedures and provides solutions to process deviations and Customer complaints. | 8/18/2019 |
| 14289 | Steris Fort Lauderdale, FL Shipping & Receiving Coordinator I HS Diploma/GED Exp: 1 or more year work experience |
Responsible for receiving and shipping medical instruments, devices, component parts and miscellaneous items into and from the repair facility by performing the following duties. This position may have responsibility for the disinfection control process of medical instruments/devices received. | 8/18/2019 |
| 14290 | Stratos Genomics Seattle, WA Laboratory Assistant I BS/BA in life sciences, engineering or chemical sciences Exp: 0-2 years |
The position is hourly (8am-5pm) with hours dependent on lab needs and project deadlines. Order and track laboratory supplies. Create, receive and reconcile orders through our ordering and tracking software. Maintain and repair equipment. Complement the positive and dynamic Central Services (CS) team, lending support to the CS manager and other laboratory assistants. | 8/18/2019 |
| 14291 | Stratos Genomics Seattle, WA Research Associate/Scientist—Molecular Engineering BS/BA or MS in chemical sciences/engineering Exp: 1-2 years lab experience |
Candidates will be involved in synthesizing the unique building blocks for our novel DNA sequencing technology, developing and optimizing synthesis protocols, as well as proposing and executing innovative experiments to push our technology forward. The position is salaried with hours dependent on lab needs and project deadlines. | 8/18/2019 |
| 14292 | AMRI Alburquerque, NM Packaging Process Technician HS Diploma/GED Exp: 3 months related experience |
The Packaging Process Technician will provide quality oversight to the packaging processes and functions during the inspection and cartoning of commercial product lots. Direct support and oversight will be provided to internal departments to ensure compliance of cGMP standards and FDA regulations. Additionally, the Packaging Process Technician will perform real time review and approval of PBRs and supporting documentation accompanying the packaging processes and work with appropriate Line leads/Supervisors to ensure documentation errors or issues are resolved. | 8/18/2019 |
| 14293 | AMRI Burlington, MA Quality Control Microbiologist (1st Shift) BS in sciences/microbiology Exp: 1 year in GMP/GLP |
The Quality Control Microbiologist is an integral part of the AMRI team and performs quality activities in support of product production and releases. The QC Microbiologist performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. | 8/18/2019 |
| 14294 | Stemia Biomarker Discovery Madison, WI Technical Sales and Marketing Associate BS or BBA in life sciences or communications Exp: 1-2 years |
Manage lead generation and tracking using the CRM Salesforce, the marketing automation system Pardot, social media platforms, web traffic tracking systems, and other marketing tools. Manage and build the current database for both business units. Create content using these marketing tools, including regular marketing emails, social media posts, website content, conference materials, print collateral, and other communications as needed for both business units | 8/18/2019 |
| 14295 | SomaLogic Boulder, CO Research Associate II MS in biology,biochemistry, chemistry or related Exp: 1 year |
The Analytical Sciences team is seeking a Research Associate to assist in the identification and characterization of SOMAmer® reagents. This position works in a fast-paced, team-oriented research group. The individual will primarily perform sample preparation of protein pulldown samples for LC-MS analysis and also generate new SOMAmer reagents using the SELEX process. Detailed documentation, critical evaluation and communication of results are essential traits for this position. Level will be commensurate with experience. | 8/17/2019 |
| 14296 | Sorrento Theraputics San Diego, CA Quality Control Microbiology Associate BS in microbiology or related Exp: 1-2 years industry experience |
This individual contributes to general operations and testing for the Quality Control and Microbiology Laboratories. This position supports in-process testing and drug substance and drug product release and stability testing programs. Environmental monitoring of cGMP cleanrooms per FDA and USP guidelines. Sampling of utilities (i.e. water, clean compressed air) | 8/17/2019 |
| 14297 | Sorrento Theraputics San Diego, CA Manufacturing Associate I BS/BA in biological/chemical sciences Exp: 0-1 year in manufacturing |
We are currently seeking a Downstream Manufacturing Associate I. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. This position will also be responsible for supporting the inventory control for the downstream group. | 8/17/2019 |
| 14298 | Sorrento Theraputics San Diego, CA Manufacturing Associate I BS in life sciences, chemistry, or chemical engineering Exp: 1-3 years in cGMP environment |
We are currently seeking a Manufacturing Associate who will be responsible for performing Upstream manufacturing tasks. Including but not limited to: Tracking & control of raw material inventory. Maintenance and operation of equipment in cGMP facilities. Preparation of buffer and media. Assistance in operation of single use bioreactors for production of clinical and commercial products. | 8/17/2019 |
| 14299 | Sorrento Theraputics San Diego, CA Research Associate / Associate Scientist, Antibody Analytics MS in chemical sciences Exp: 1-2 years |
As an Associate Scientist you will work in the Antibody Analytics group and be responsible for the development, implementation and maintenance of a variety of analytical assays to support R&D in protein therapeutics including monoclonal antibodies, bispecific antibodies, antibody-drug conjugates (ADC) and CAR-T. These assays include but not limited to chromatography (SEC, IEX, HIC and RP), electrophoresis (SDS-PAGE and CE-SDS), and icIEF | 8/17/2019 |
| 14300 | Sepectrum Pharmaceuticals Irvine, CA Clinical Trials Assistant HS Diploma/GED Exp: 1-2 years clinical study experience |
Provide support to the Clinical Trial Managers and Clinical Research Associates in clinical trial conduct via preparation, distribution, and tracking of study supplies, mass mailings, copying, data entry, etc. Recognize the urgency of meeting established schedules and be able to prioritize tasks and time to meet those schedules. Develop materials that support the conduct of clinical studies including: site reference manuals, monitoring flow sheets, CRF completion guidelines, etc.)Demonstrate superior communication and organizational skills in addition to the technical skills required for overseeing clinical studies. | 8/17/2019 |
| 14301 | Spherotech Lake Forest, IL Quality Control Associate BS in chemistry or related Exp: 1 or more years |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. | 8/17/2019 |
| 14302 | Sprint Cleveland, OH Quality Assurance Specialist BS in engineering, science or related Exp: 1-2 years in med devices |
Works with the Quality Assurance team in the processing of product complaints, including coordination of product returns. Assists with supplier approval and monitoring. Initiates and conducts CAPA (Corrective and Preventative Action) activities. Supports audits and FDA inspections. | 8/17/2019 |
| 14303 | Repligen Rancho Dominguez, CA Assembler I HS Diploma/GED Exp: 0-1 years production/manufacturing |
This assembly position performs a wide variety of fiber assembly, filtration product assembly or sub-assemblies. Determines and/or follows methods and sequence of operations in performing fiber bundling, filter potting, filter welding, fitting on assembly units and packaging. The employee also works as a team member in whatever capacity and job function is required to deliver a quality product to our customer in a timely fashion. | 8/17/2019 |
| 14304 | SevenBridges San Francisco, CA Technical Support Engineer BS/BA in computer science or related Exp: 1+ years |
Your main role will be to work with our developers, bioinformaticians as well as our clients, on removing obstacles and helping users troubleshoot issues, resolving or escalating problems to engineering teams. Technical Support Engineers will work with our cross-functional team as a part of our Product division in Seven Bridges. Working on production database/microservices (e.g. making mass changes using Seven Bridges API, scripts or SQL) independently and confidently . | 8/16/2019 |
| 14305 | Siemens Richland, MS Manufacturing Engineer - Entry Level BS in electrical or mechnical engineering Exp: 0-2 years |
The candidate will get rotated through all the departments in the plant and once that has been completed you will be assign to the department that best fits the needs of the plant and is a fit for your background. Potential experiences include product design, customer order engineering, application engineering, quality engineering and manufacturing engineering. | 8/16/2019 |
| 14306 | Siemens Richland, MS Quality Engineer - Will Consider Entry Level BS in Electrical, Mechanical, or Industrial Engineering Exp: Entry Level |
This position is in the Quality Department in Richland, MS reporting to the Quality Manager. The position is accountable for ensuring product/process integrity for high voltage circuit breakers through the development and implementation of systems that support internal processes such as the nonconformance system, final or in-process inspections, root cause analysis, 8D corrective actions, and other QC related activities. | 8/16/2019 |
| 14307 | Siemens Ames, IA Software Engineer BS in Engineering, Math, Computer Science Exp: 1+ years in C++ |
Software Engineer needed to join the Teamcenter Visualization development team, with most team members located in Ames, Iowa. Design, develop, maintain and test software programming for Siemens PLM products with focus on achieving high quality and on time delivery of the software solution. Ensure the overall functional quality of the released product on all required platforms. | 8/16/2019 |
| 14308 | Siemens Enid, OK Service Technician HS Diploma/GED Exp: 0.5-1 year or more as wind technician |
The Field Service Technician performs planned and unplanned maintenance including troubleshooting and replacement of parts if necessary in a safe and professional manner on Wind Turbines. Detailed records and parts used must be completed for all work performed. Technicians report to site management and communicate needs and or safety issues that arise. Perform first class work on preventive maintenances to be completed on time and right the first time. | 8/16/2019 |
| 14309 | Siemens Richland, MS Engineering Management Acceleration Program BS in mechnical, aerospace, chemical, or electrical engineering Exp: New Graduate, 3.2 or higher GPA |
The Engineering Management Acceleration Program (EMAP) is a five-year development opportunity for entry-level candidates with potential for rapid advancement in the Siemens Oil & Gas business. EMAP prepares you to become a future leader of Siemens Oil & Gas by providing unique work experience, training, and mentorship. Jump start your career today! | 8/16/2019 |
| 14310 | SightLife Seattle, WA Research Associate BS in related field Exp: 1 or more years in lab |
Responsible for aiding in the continued research and development of current and future activities and projects related to corneal transplantation and cell therapy following GCP and GMP guidelines. Design and execute laboratory processes according to established protocols. Maintain records of observations and interpret findings. Continually assess procedures and look for process improvements. Organize and store all chemical substances, fluids and compressed gases according to safety instructions. | 8/16/2019 |
| 14311 | SightLife Seattle, WA Operations Business Analyst BS/BA in related field Exp: 0-2 years in operations |
This position is responsible for collaborating with Operations teams and Technology Services to plan, design, develop and deploy new technology solutions while maintaining and enhancing existing systems for Operations. This includes gathering and analyzing data, process flows and business requirements in support of business cases and proposed projects and working closely with management and staff across Operations in all SightLife locations to maximize use of resources and technology solutions. | 8/16/2019 |
| 14312 | SightLife Boston, MA Laboratory Support Technician AS/AA in allied health fields Exp: 0-2 years |
Under the direction of the Technical Program Manager and Director at CorneaGen - Boston, the Laboratory Support Technician will assist in tissue processing and distribution related operations, and tissue suitability activities. The incumbent will be expected to steward each donor’s Gift by ensuring standardized operational practices are effectively executed at the local level and by seeking continual improvement opportunities to maximize the value of the Gift | 8/16/2019 |
| 14313 | Sinclair Research Auxvasse, MO Veterinary Technician BS/BA, Registered Vet Tech or HS Diploma Exp: BS/BA: 0 years, HS: 1 year |
Our Veterinary Technicians are critical in bridging study procedures from Operations to Veterinary Services. They will participate in activities relating to both departments by assisting in blood collections, catheter placement, anesthesia monitoring, collecting samples and administering dosing, and supporting veterinary staff in overseeing herd health. More advanced technicians will also assist during surgical procedures or perform minor procedures themselves, administer advanced dosing, and perform advanced collection procedures. | 8/16/2019 |
| 14314 | Smith Nephew Columbia, MD Donor Eligibility Associate BS/BA in life sciences Exp: 1 or more year in hospital/biotech/GTP environment |
The primary purpose of this position is to receive, assemble, review, and assess the donor recovery records (donor chart) against current tissue bank standards, applicable tissue regulations, and Osiris criteria in order to help determine donor eligibility. | 8/16/2019 |
| 14315 | Smith Nephew Columbia, MD Manufacturing Technician AS/AA in life sciences Exp: 1-2 years in GMP environment |
Responsible for hands-on execution of all activities in the manufacturing area including the processing and packaging of human tissue products for transplantation. All duties are performed in compliance with FDA cGMP/cGTP requirements, American Association of Tissue Banks (AATB) standards, and Osiris Therapeutics Inc. standard operating procedures (SOPs). | 8/16/2019 |
| 14316 | Smith Nephew Fort Worth, TX Quality Engineer I BS in engineering, biomedical or industrial engineering Exp: |
Responsible for assisting to improve the Quality Compliance of Fort Worth and TJ Smith & Nephew QMS. Primary responsibilities include assisting with Risk Management, Design History Files, Product Release, and revision of documents in the DMS. Works within the quality management systems and ensuring functional compliance to the applicable FDA’s cGMPs, international standards, Good Distribution Practices and state requirements (Smith & Nephew and outsource suppliers). | 8/16/2019 |
| 14317 | Smith Nephew Memphis, TN Quality Assurance Inspector 1 HS Diploma/GED Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. | 8/16/2019 |
| 14318 | Smith Nephew Columbia, MD Quality Assurance Inspector 1 HS Diploma/GED Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. | 8/16/2019 |
| 14319 | Smith Nephew Columbia, MD Quality Assurance Inspector 1 HS Diploma/GED Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions | 8/16/2019 |
| 14320 | Smithers Wareham, MA Laboratory Assistant HS Diploma/GED Exp: 0 years required |
Individual is expected to perform a variety of routine tasks in support of the conduct of normal laboratory operations and similar duties as assigned. Also responsible for cleaning laboratory glassware and equipment, as well as stocking and requesting laboratory supplies. Maintains the cleanliness of the laboratory including but not limited to sweeping and washing the floor, cleaning bench tops, fume hoods. Individual disposes of chemical and solid waste. Responsible for the development of familiarity with routine assignments and laboratory practices. | 8/16/2019 |
| 14321 | Smithers Wareham, MA Entry Level Technical Report Writer BS/BA in environmental sciences Exp: 0-2 years lab experience |
The candidate will be responsible for writing and editing high quality study reports for several technology groups, including ecotoxicology, environmental fate and metabolism, avian and analytical chemistry, in addition to production of other documents as needed. Prepares study reports from data presented in technical format that meets guideline requirements. Compiles and incorporates comments from several different levels of review. | 8/16/2019 |
| 14322 | Smithers Lansing MI, MA Product Testing Technician HS Diploma/GED Exp: 1-5 years of mechanical background/training |
Performs laboratory tests to determine physical characteristics of materials and products for such purposes as quality control, process control or product development by performing essential duties and responsibilities. Perform testing in accordance with relevant specification(s). Follow daily work assignments relative to test schedule. | 8/16/2019 |
| 14323 | Singota Solutions Bloomington, IN Associate Quality Control Analyst BS in chemistry or related Exp: 1 or more year in formulation, testing, or research |
Support the Quality Control function with respect to raw material, in-process, release and stability testing. Collaboratively participates in Development functionsfor the company including pre-formulation, formulation, process and analytical development activities. Operate various lab instruments and equipment including (but not limited to): Karl Fisher, pH, HPLC, FTIR, UV-VIS, DSC, TOC, Lab-ware washers, Autoclave, Laminar Flow Hoods, Bio-Hazard Hood, Microbalances, and other diverse lab equipment and various wet chemistry techniques. | 8/16/2019 |
| 14324 | Tolmar Windsor, CO Manufacturing Technician I - Derms HS diploma or equivalent Exp: None required |
Assist in the set up and operation of all final packaging equipment (cartoners). Properly load subcomponents into final packaging equipment. Accurately document production activities using regulatory controlled documents including production records and log books. Perform facility cleaning of manufacturing areas as required to maintain a cGMP environment and in accordance with Standard Operating Procedures. Properly perform the Done By function on batch records in accordance with cGMP standards. Ensure that product quality adheres to approved specifications. etc. | 8/13/2019 |
| 14325 | Tolmar Fort Collins, CO Material Handler / Warehouse - 1st, 2nd and 3rd shift HS diploma or equivalent Exp: 1+ years |
This position requires the flexibility to function in all three areas: Material Handling, Shipping Clerk and Receiving Clerk: Material Handler: Verify quantities, lot numbers, and part numbers against documentation previously prepared. Issue and move components, supplies and printed materials from the warehouse to meet manufacturing and intra-company requirements. Stage raw materials for Issuance Group dispensing. Assist in raw materials dispensing as required. Verify and receive materials returned from manufacturing in a timely manner. etc. | 8/13/2019 |
| 14326 | Tolmar Windsor, CO MF Operator I - Bulking 2nd shift HS diploma or equivalent Exp: 1+ years |
Properly perform job duties with a second checker present. Assist in set up and operation a variety of mixing, weighing and pumping equipment used to produce bulk dermatological product. Perform the routine production of bulk dermatological products per applicable batch production records. Perform the transfer of bulk material from mixing containers into storage containers. Document the verification of production activities using regulatory controlled documents including production records and log books. etc. | 8/13/2019 |
| 14327 | Tolmar Fort Collins, CO Manufacturing Technician I - Injectables (2nd shift) HS diploma or equivalent Exp: None required |
Assist in the set up and operation labeling equipment used to label pre-filled syringes and/or vials, including equipment in the sterile support areas. Properly load pre-filled syringes and/or vials into labeling equipment. Assist in the set up and operation of semi-automatic packaging equipment used to package pre-filled syringes. Properly load pre-filled syringes and components into semi-automatic packaging equipment. Accurately document production activities using regulatory controlled documents including production records and log books. etc. | 8/13/2019 |
| 14328 | Tolmar Fort Collins, CO Manufacturing Operator I - Derm - 1st shift HS diploma or equivalent Exp: 1+ years |
Properly perform the Done By function on batch records in accordance to cGMP standards. Assist in the set-up of semi-automatic filling equipment used to fill dermatological products. Operate fast-paced, basic production equipment with manual loading processes. Perform routine sampling and inspections for product attributes (fill weights, product sealing, labeling) of filled products. Assist in the set-up of semi-automatic labeling equipment used to apply labeling to pre-filled jars, bottles and vials. etc. | 8/13/2019 |
| 14329 | Tolmar Windsor, CO Manufacturing Technician I - Aseptic (2nd Shift, Mon - Thurs) HS diploma or equivalent Exp: None required |
Assist in the set up and operation labeling equipment used to label pre-filled syringes and/or vials, including equipment in the sterile support areas. Properly load pre-filled syringes and/or vials into labeling equipment. Assist in the set up and operation of semi-automatic packaging equipment used to package pre-filled syringes. Properly load pre-filled syringes and components into semi-automatic packaging equipment. Accurately document production activities using regulatory controlled documents including production records and log books. etc. | 8/13/2019 |
| 14330 | Tolmar Windsor, CO Stability Associate I BS in scientific discipline Exp: 1+ years |
Purpose and Scope: Responsible for maintaining the following systems and/or databases: Stability System II Software, stability database, stability variances, stability environmental chambers, stability reports, data entry, data auditing and stability records. Essential Duties & Responsibilities: Requisition, label and place stability samples into appropriate storage conditions according to approved protocols. Enter new lots into the Stability System II Software and stability databases, and audit study start documentation. | 8/13/2019 |
| 14331 | Toxikon Bedford, MA Histology Laboratory Assistant HS diploma Exp: Entry level |
Toxikon is seeking an entry level lab assistant to work in the In Histology. The successful candidate will have interaction with Histology Research Associates, Histology Study Directors, Vet Care staff and interface with laboratory management regarding all day-to-day activities of the studies. They will be responsible for providing logistical support for the studies being conducted. As a laboratory assistant, you will be responsible for preparing animals for the studies conducted, including shaving, weighing and identification. Additionally, you will be responsible to ensure the technical conduct and regulatory compliance of your duties comply with FDA GLP and ISO regulatory guidelines. etc. | 8/13/2019 |
| 14332 | Toxikon Bedford, MA Histology Research Associate AS/BS in life sciences Exp: No previous experience required |
Toxikon is currently seeking a full-time Histology Research Associate. Qualified candidates should be a team player, have a willingness to learn, be detail oriented, proficiency with computers and have well-developed time management skills. Essential Duties: Trimming of tissues and organs harvested at necropsy. Embedding and processing of tissues. Microtomy Routine H&E staining, other stains as required. Maintain and/or create GLP documentation as necessary, including relative SOPs and histology records, Maintain wet tissue archive. etc. | 8/13/2019 |
| 14333 | Toxikon Bedford, MA Laboratory Assistant, In-Vivo HS diploma Exp: Entry level |
Toxikon is seeking an entry level lab assistant to work in the In Vivo Biocompatibility department. The successful candidate will haveinteraction with In Vivo Research Associates, In Vivo Study Directors, Vet Care staff and interface with laboratory management regarding all day-to-day activities of the studies. They will be responsible for providing logistical support for the studies being conducted. As a laboratory assistant, you will be responsible for preparing animals for the studies conducted, including shaving, weighing and identification. Additionally, you will be responsible to ensure the technical conduct and regulatory compliance of your duties comply with FDA GLP and ISO regulatory guidelines. etc. | 8/13/2019 |
| 14334 | Tris Pharma Monmouth Junction, NJ Method Validation Scientist MS Exp: 1 year |
We have a unique opportunity for an entry level to intermediate Scientist to perform laboratory analyses in the testing of raw materials for release, in process (IP), finished products (FP) during process validation and stability (ST) samples of test batches and to carry out laboratory work to support method validation activities. This position is located at our Monmouth Junction, NJ facility. Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws. Operates general analytical instruments during raw material, in process and finished product testing such as HPLC, GC, UV/Vis, automatic titration, IR, AA, TLC and dissolution apparatus.We have a unique opportunity for an entry level to intermediate Scientist to perform laboratory analyses in the testing of raw materials for release, in process (IP), finished products (FP) during process validation and stability (ST) samples of test batches and to carry out laboratory work to support method validation activities. This position is located at our Monmouth Junction, NJ facility. Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws. Operates general analytical instruments during raw material, in process and finished product testing such as HPLC, GC, UV/Vis, automatic titration, IR, AA, TLC and dissolution apparatus. | 8/13/2019 |
| 14335 | Tris Pharma Monmouth Junction, NJ Product Development/Formulation Scientist I MS Exp: 1 year |
RESPONSIBILITIES: Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws. Reverse engineering of existing marketed product with respect to physical and chemical characterization. Preformulation studies including drug-excipient compatibility studies. Preparation of formulation batches on laboratory scale and submitting samples for chemical analysis. etc. | 8/13/2019 |
| 14336 | Tris Pharma Monmouth Junction, NJ Quality Control Chemist BS in chemistry Exp: 1 year |
QC Chemists perform analytical testing of raw materials, packaging component, in-process, finished product, stability samples, cleaning verification/validation, and process validation samples following Analytical Methods, Protocols, Procedures (SOP’s) and company policies. He/she follows and maintains adherence to current industry standards (cGMP’s, GLP’s, etc.) to meet production and customer demand. Qualified candidates will be expected to work either independently or as a team to achieve company goals and initiatives. etc. | 8/13/2019 |
| 14337 | Trucode Gene Repair South San Franscisco, CA Associate Scientist MS Exp: 1-2 years |
Trucode Gene Repair Inc. is a stealth-mode therapeutics development company pioneering a novel synthetic gene editing technology to treat and cure patients with devastating rare diseases. We seek a highly skilled, motivated and creative chemist ready to function in a fast-paced and collaborative environment. Candidates should have exceptional solid phase peptide synthesis and/or HPLC analysis and purifications training. The successful candidate will be part of a dynamic and rewarding work environment where the abilities to effectively communicate and function in a team environment will be essential for success. etc. | 8/13/2019 |
| 14338 | Tunnell King of Prussia, PA Analyst BS/BA in engineering Exp: 0-4 years |
The Systems Support Specialist – Operational Technology will provide basic technical support for manufacturing and manufacturing support systems in a regulated, validated environment. Provide first level technical support of manufacturing and manufacturing support systems including but not limited to; answering questions, resetting passwords Troubleshoot and maintain OT computers, peripheral equipment and software Work with vendor support contacts to resolve technical hardware and / or software problems, escort vendors on the premises, answer basic questions, oversee work being performed Enter, update and follow up supp+H10:H14ort requests in OT’s issue tracking system Provide first level systems training to end users Other duties as assigned | 8/13/2019 |
| 14339 | Tunnell unspecified, MD Manufacturing Associate II BS in scientific or engineering field Exp: 1-3 years |
The Manufacturing Associate is responsible for supporting the overall GMP upstream manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II & commercial GMP manufacturing. Key Responsibilities include but are not limited to: Completes Batch Production Records under cGMP, and documents in detail through the use of SOPs and BPRs for the processes and manufacturing steps. Generates operational protocol(s), internal or external documents including SOPs, BPRs, deviations and summary reports. | 8/13/2019 |
| 14340 | Turning Point Therapeutics unspecified, Clinical Trial Associate BA/BS Exp: 1-3 years |
We are seeking a highly motivated individual to join TP Therapeutics as a Clinical Trial Associate (CTA) within the Clinical Operations Team, reporting into the Director of Clinical Operations. The Clinical Trial Associate is responsible for the oversight and management of clinical operations activities or projects. The CTA will interact with Clinical Operations teams and collaborate effectively with CROs, vendors and clinical trial sites. The CTA supports the timely conduct of clinical studies according to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and all applicable regulations governing the conduct of clinical trials. etc. | 8/13/2019 |
| 14341 | United Animal Health Sheridan, IN Laboratory Assistant (Part-Time) HS diploma or experience Exp: None required |
The Lab Assistant will be responsible for processing samples, performing routine tests and assisting other laboratory staff. An ideal candidate will possess strong time management skills, have a high attention to detail and be able to effectively communicate with others in the lab. This is a part-time (20-24 hours/week) position with flexible hours within the operating hours of the Lab (Monday-Friday 8-5). etc. | 8/13/2019 |
| 14342 | United Therapeutics Research Triangle Park, NC System Support Specialist - Operational Technology BS in information techology, engineering, or business administration Exp: 1+ years |
The Systems Support Specialist – Operational Technology will provide basic technical support for manufacturing and manufacturing support systems in a regulated, validated environment. Provide first level technical support of manufacturing and manufacturing support systems including but not limited to; answering questions, resetting passwords. Troubleshoot and maintain OT computers, peripheral equipment and software. Work with vendor support contacts to resolve technical hardware and / or software problems, escort vendors on the premises, answer basic questions, oversee work being performed. Enter, update and follow up support requests in OT’s issue tracking system. Provide first level systems training to end users. Other duties as assigned. | 8/13/2019 |
| 14343 | United Therapeutics Silver Spring, MD Process Engineer BS Exp: 1+ years |
We are currently looking for a Process Engineer to join our API team. In this role, you will support the process engineering team in the specification, installation, maintenance and operation of small-molecule API production equipment and processes. Additionally, you will partner with members of the API Production and R&D team on activities as required to help internal customers efficiently produce the best medicines possible. etc. | 8/13/2019 |
| 14344 | Unum Therapeutics Cambridge, MA Associate Scientist - Bioassay (Immunology) MS in cell and molecular biology or related discipline Exp: 1-3 years |
The primary role as an Associate Scientist will be to use and develop immunoassays and bioassays to enhance understanding of key attributes in support of cell therapy process and product development and characterization. Participate in activities to support Unum’s pipeline within established timelines and ensure data quality and integrity. Participate in design and execution of experiments and complete laboratory testing. Analyze and present experimental data at departmental and company meetings. Follow good documentation and review practices, and effectively communicate scientific results in presentations and written reports. Draft standard operating procedures and test protocols in support of analytical development. | 8/13/2019 |
| 14345 | Unum Therapeutics Cambridge, MA Associate Scientist , Translational Medicine MS in biology, immunology or oncology Exp: 1-4 years |
What will you be doing? Support the development, execution and analysis of assays in early clinical studies to assess ACTR T cell persistence and phenotype, target expression/occupancy, cytokine levels and immunogenicity. Explore predictive biomarkers of ACTR manufacturing and clinical success across various patient populations. Prepare data packages for technical reports, SOPs, and regulatory submissions. Manage the transfer of technical protocols to contract testing labs. Work collaboratively across internal discovery, manufacturing and clinical groups, external collaborators and contract research organizations. | 8/13/2019 |
| 14346 | Vapotherm unspecified, Accounts Receivable Associate AS/AA Exp: 1-3 years |
Reporting to the AR Manager, this position will be responsible for invoicing and performing collections duties. Collections activities will include but not be limited to maintaining the Billtrust system, processing credit cards, the review of past due accounts, calling customers for payment, communicating internally and externally regarding repayment status, and assisting in maintaining a targeted DSO. etc. | 8/13/2019 |
| 14347 | Varian Palo Alto, CA Service Desk Agent / Associate (Japanese) BA/BS Exp: 6 months - 1 year |
Addresses and resolves basic incidents and requests; logs all incidents and requests; engages other service desk resources or appropriate service resources to resolve incidents that are beyond the scope of their ability or responsibility. Uses the appropriate categories for logging incidents and requests. Creates a positive customer support experience and builds strong relationships through deep problem understanding, ensuring timely resolution or escalation, communicating promptly on progress, and handling customers with a consummately professional attitude. Ensures the end-to-end customer experience and provides a single point-of-contact for the customer. Analyzes and resolves incidents and requests regarding use of application software or hardware. etc. | 8/13/2019 |
| 14348 | Upsher-Smith Maple Grove, MN Corporate Sales Associate BA/BS in business, science, communication, or related Exp: 0-1 years |
The Corporate Sales Associate is responsible for developing proficiency in the development and management of a designated territory with the goal of maximizing sales while improving patient lives. Patients are central to all USL strategies, and the CSA will be responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other healthcare practitioners and members of the health care community. The CSR may work in a team with a Corporate Sales Specialist (CSS), Regional Trainer, Managed Care - Regional and National Account Manager to increase sales, market share and profitability of USL products. Time allocation of 75% inside sales and 25% field sales is expected; however, this may vary as business needs arise. | 8/13/2019 |
| 14349 | Upsher-Smith Maple Grove, MN Lab Tech I HS diploma or equivalent Exp: 0-2+ years |
The Lab Tech performs routine analytical physical attribute testing. Assists laboratory analysts with solution preparation, simple sample preparation, and clean up as requested. Disposes of laboratory hazardous waste as necessary. Performs routine maintenance on select laboratory equipment and ensures laboratory safety-equipment is functioning properly. Familiar with basic laboratory techniques (e.g. pipetting, weighing, pH). Documents all laboratory work according to internal SOPs, test methods, and cGMPs. etc. | 8/13/2019 |
| 14350 | Upsher-Smith Plymouth, MN Packaging Tech I - 1st Shift HS diploma or equivalent Exp: 1 year |
The Packaging Tech II - 1st shift (5:00 AM - 1:15 PM) is responsible for demonstrated expertise on one or multiple production lines and to ensure safe, quality pharmaceutical product packaging. This position sets up, adjusts and troubleshoots pharmaceutical packaging machinery and ensures that packaging operations are completed per standard operating procedure. etc. | 8/13/2019 |
| 14351 | Upsher-Smith Plymouth, MN Packaging Tech II - 2nd Shift HS diploma or equivalent Exp: 1 year |
The Packaging Tech II - 2nd shift (1:00 PM - 9:15 PM) is responsible for demonstrated expertise on one or multiple production lines and to ensure safe, quality pharmaceutical product packaging. This position sets up, adjusts and troubleshoots pharmaceutical packaging machinery and ensures that packaging operations are completed per standard operating procedure. etc. | 8/13/2019 |
| 14352 | Upsher-Smith Plymouth, MN Packaging Tech II - 3rd Shift HS diploma or equivalent Exp: 1 year |
The Packaging Tech II - 3rd shift (9:00 PM - 5:15 AM) is responsible for demonstrated expertise on one or multiple production lines and to ensure safe, quality pharmaceutical product packaging. This position sets up, adjusts and troubleshoots pharmaceutical packaging machinery and ensures that packaging operations are completed per standard operating procedure. Essential Duties: Executes packaging line operations, processes and procedures. Coordinates the packaging efforts for designated production lines and teams. Completes machine set up, operations, tooling changes, adjustments and troubleshooting related to the operation of one or more packaging lines. etc. | 8/13/2019 |
| 14353 | TriLink San Diego, CA Manufacturing Associate II BS in life sciences or related Exp: 1+ years |
TriLink Biotechnologies is seeking a Manufacturing Associate II who will produce research and clinical grade components and products within ISO 5 and greater environments. The candidate will participate in the set-up, cleaning, operation, and maintenance of laboratory equipment; perform chemical and enzymatic reactions following aseptic procedures. The candidate must document all actions using GMP Good Documentation Practices. This position requires a candidate that can excel as a leader in the laboratory space. etc. | 8/13/2019 |
| 14354 | Sarepta Therapeutics Columbus, OH Laboratory Veterinarian Technician HS Diplomga/GED Exp: 1-2 years |
Handle, transfer, and distribute mice, supplies and waste as needed to and from work area(s). Proficient in IM, IV, IP administration techniques in lab animals. Coordinate with vendors and supervisors on operational, administrative and technical responsibilities. Monitor the daily health and welfare of the animals according to IACUC guidelines | 8/11/2019 |
| 14355 | Sarepta Therapeutics Columbus, OH Research Associate I, Histology, Gene Therapy Research AS/AA in chemical, physical or biological sciences Exp: 1-3 years |
The qualified candidate will provide laboratory support of day-to-day GCP/GLP testing on muscle/nerve using complex histology methods in accordance with the requirements of approved protocols; maintains records of experiments; assists in analyzing data and prepares laboratory reports. This person may participate in development, GCP/GLP qualification, and validation of histology related assays to support clinical trials and clinical development decision-making. | 8/11/2019 |
| 14356 | SCIEX Carlsbad, CA Production Scientist I BS/BA in biological or chemical sciences Exp: 1-2 years lab experience |
Performs simple calculations according to procedures, and maintains accurate records of work performed according to GLP, GMP, and QSMRs. Manufacturing of Life Science products according to standard operating procedures and work instructions. Independently prioritize work assignments and consistently demonstrate the ability to perform assigned tasks in manufacturing setting | 8/11/2019 |
| 14357 | Seattle Genetics Bothell , WA QC Analyst I/II, Potency Analyst BS/BA in life sciences Exp: 0-4 years in pharma/biotech |
This position is located within the Quality Control department and is responsible for all programs release and stability testing, by performing potency methods such as cell-based assays and binding assays. | 8/11/2019 |
| 14358 | Seattle Genetics Bothell , WA QC Analyst I/II, Analytical BS/BA in sciences Exp: 0-4 years in pharma/biotech |
This position is located within the Quality Control department and is responsible for all programs release and stability testing, by performing analytical methods such as HPLC/ UPLC, Capillary Electrophoresis (CE), etc. | 8/11/2019 |
| 14359 | Seattle Genetics Bothell , WA Process Chemistry MS in chemistry Exp: 0-5 years |
The successful candidate will be responsible for developing novel synthetic routes and chemical processes for anti-cancer drugs and proprietary drug linkers used for antibody conjugation. The ideal candidate should possess an in-depth knowledge of organic chemistry, reaction mechanisms, and familiarity with modern synthetic methods and analytical techniques. Candidates will have demonstrated creativity and independence in solving synthetic problems and ultimately developing robust chemical processes which he or she will work to transfer to CMO’s. Experience and expertise in peptide synthesis is desirable. | 8/11/2019 |
| 14360 | Seattle Genetics Bothell , WA Formulation and Drug Product Sciences BS in biochemistry, engineering, chemistry or biological sciences Exp: 0-2 years |
The Formulation and Drug Product Sciences Group at Seattle Genetics is seeking a highly motivated Research Associate to assist in the formulation development for therapeutic antibodies and antibody-drug conjugates. Conduct experiments and analyze results leading to development of robust formulations for antibodies and antibody drug conjugates | 8/11/2019 |
| 14361 | Seattle Genetics Bothell , WA BioProcess Development BS/BA in chemistry, biochemistry, biological sciences Exp: 0-2 years |
The BioProcess Development Department at Seattle Genetics is seeking a Research Associate to participate in the purification development efforts to support process development for our antibody and antibody-drug conjugate programs. | 8/11/2019 |
| 14362 | Seattle Genetics Bothell , WA Shipping & Receiving Associate I HS Diplomga/GED Exp: 0-4 years |
Responsible for receipt, storage, and delivery of laboratory supplies & equipment, office supplies and other products such as break room supplies. Shipping & Receiving Associates I must demonstrate meticulous attention to detail, flexibility and a willingness to perform a wide variety of tasks while adhering to defined procedures. The position will work directly with the Purchasing, Research & Development, and Finance departments to accurately track, record, deliver and maintain the correct amount of supplies and equipment to the correct locations at all times. | 8/11/2019 |
| 14363 | Sebela Boston, MA QC Chemist BS in chemistry or related Exp: 0-2 years |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. Perform testing of raw materials and products. Perform instrument qualification and maintenance. Review analytical data for completeness, accuracy, and compliance | 8/11/2019 |
| 14364 | Sedia Portland, OR QC Technician HS Diplomga/GED Exp: 1 or more years in lab |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. Demonstrates a high level of independent judgment and discretion in the timely identification, investigation and resolution of events impacting the Quality of products and processes. | 8/11/2019 |
| 14365 | Sedia Portland, OR Manufacturing Technician HS Diplomga/GED Exp: 1 or more year in lab |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. The Manufacturing Technician will adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance. | 8/11/2019 |
| 14366 | Sedia Portland, OR Scientist/Associate Scientist (R&D Product Development) MS in biological sciences or engineering Exp: 1-3 years |
The successful candidate will be responsible for running laboratory tests, recording data, performing some degree of data analysis, drafting protocols, and communicating with managers from R&D and other departments. They will also be asked to participate in production of prototype products, and assist in transition of those procedures (through training and/or record-keeping) to our manufacturing department. | 8/11/2019 |
| 14367 | Semma Therapeutics Cambridge, MA Quality Control Associate (MA) MS/MA in sciences Exp: 1+ years |
This position will perform QC tests for pre-clinical and clinical material from specific manufacturing steps associated with ES-derived pancreatic Islets production, from cell bank thaw through fill/finish. QC testing will include stability tests for cell banks and final product, in-process manufacturing tests and final product lot release tests. The candidate will be expected to assume additional QC testing responsibilities associated with specific projects (e.g. cold chain custody qualification, in-use stability testing, etc). | 8/11/2019 |
| 14368 | Semma Therapeutics Cambridge, MA Research Associate – Discovery Cell Biologist R&D BS in sciences Exp: 1-2 years lab experience |
he full-time role will focus on tissue culture, molecular and cellular characterization, and assay development. Under the supervision of a Senior Scientist the associate will be responsible for the day-to-day execution of specific projects in coordination with members of the Process Development team. | 8/11/2019 |
| 14369 | Semma Therapeutics Cambridge, MA Research Associate – Cell Biologist R&D BS or MS in cell/molecular biology Exp: 1-2 years |
The full-time role will focus on tissue culture, molecular and cellular characterization, and assay development. Under the supervision of a Senior Scientist the associate will be responsible for the day-to-day execution of specific projects in coordination with members of the Discovery Biology team. | 8/11/2019 |
| 14370 | Semma Therapeutics Cambridge, MA GMP Manufacturing Associate, Clinical Materials BS in biological/bioengineering sciences Exp: 0-1 years in development/manufacturing |
This full-time role reports to the Director of Manufacturing, and will be responsible for the technology transfer and production of cell therapy products to support Semma’s Phase I/II clinical trials. Clinical materials produced in the facility will be manufactured according to Good Manufacturing Practices (GMP) and conducted under Investigational New Drug (IND) applications with the US Food and Drug Administration (FDA). | 8/11/2019 |
| 14371 | Sera Care Milford, MA Research Associate II MS in biochemistry or molecular biology Exp: 0-1 years |
Perform general molecular techniques such as plasmid purification, gel-electrophoresis, RNA transcription, and bacterial culturing. Perform nucleic acid analysis (RNA/DNA integrity analysis, real time qPCR, digital PCR) and analyze results. Work with supervisor to plan and execute new projects as assigned according to the timelines and ensure documentation meets GLP/GMP requirements. Record test results and data records, seek appropriate approval and file according to established procedures. | 8/11/2019 |
| 14372 | Renaissance Lakewood, NJ Manufacturing Coordinator HS Diplomga/GED Exp: Entry Level |
The Manufacturing Coordinator supports the Process Supervisor in the daily activities of union and non-union personnel in the filling and packaging of sterile and specialty pharmaceutical products in compliance with FDA regulations and cGMP guidelines. Responsible for the proper operation of all production activities assigned such as scheduling and training. This includes but is not limited to: preparing, staffing, and operating production line and safety. This is a swing shift position from 10:30 am to 7:00 pm. | 8/10/2019 |
| 14373 | Philips Bothell, WA Manufacturing Engineer BS in engineering Exp: 1-3 years |
In this role, you have the opportunity to manage the manufacturing of Philips AED products. Within this role, you will have end-to-end responsibility for a production line, which included part delivery, manufacturing and test flows and packaging. You will implement and validate the changes required to meet maintain compliance with Internal documents and regulated industry requirements. | 8/10/2019 |
| 14374 | Philips Carlsbad, CA Quality Engineer-CAPA BS in engineering Exp: 1 or more year with CAPA |
As the incumbent of this Quality & Regulatory (Q&R) role within Philips, your challenge will be to guide and support Business Groups, Markets and enabling functions to always do the right thing. This involves being a confident advisor on approval, regulatory compliance and quality management related topics, in order to achieve timely releases of innovative products that deliver high quality and outstanding reliability to the lives they will improve. | 8/10/2019 |
| 14375 | Revance Newark, CA Clinical Trial Associate (Contract) BS/BA in life sciences Exp: 0-2 years |
On special assignment: assist in operational and logistical tasks of clinical trials, performed according to operational best practices and quality standards (ICH GCP/ Country and Local requirements/ Company SOPs). Provide support across the Clinical department. | 8/10/2019 |
| 14376 | Rocket Pharma New York, NY Laboratory Manager/Research Technician BS or MS in biological/health sciences Exp: 1-2 years |
Experienced and motivated lab manager and research technician to assist with daily operations of a dynamic gene therapy research lab and support development activities. The position involves managing day-to-day lab activities, including but not limited to purchase and organization of reagents and supplies, maintenance of lab equipment, and simple experimental and administrative support to a dedicated team of scientists. | 8/10/2019 |
| 14377 | RTI Surgical Alachua, FL BMS Laboratory Technician HS Diplomga/GED Exp: 1 or more years in lab |
Maintains accurate records of all specimens received or sent out of the laboratory. Completes test request forms and enters the information into the Laboratory Information System. Performs specimen preparation for testing and archiving. Makes determinations as to acceptability of specimens, and files appropriate specimen rejection forms and revision request forms when necessary. Performs non-licensed testing, interprets non-licensed testing results, and prepares reports | 8/10/2019 |
| 14378 | RTI Surgical Alachua, FL Quality Engineer AS/AA or BS/BA in engineering Exp: 0-3 years |
This position is responsible for support to the quality team with task responsibility. This will involve modeling and detailing inspection prints, contributing individually and within cross-functional teams, and general project support. They will be a self-starter, have a hands-on approach in performing their work duties, and be able to work independently. This position will help RTI Surgical maximize the amount of patients served while maintaining a high level of quality and safety. | 8/10/2019 |
| 14379 | RTI Surgical Alachua, FL Supplier Quality Engineer AS/AA or BS/BA in engineering Exp: 0-3 years |
This position is responsible for support to the quality team for purchasing controls and sourced materials and services. This will involve supporting relationships with suppliers, contributing individually and within cross-functional teams, and general project support. They will be a self-starter, have a hands-on approach in performing their work duties, and be able to work independently. This position will help RTI Surgical maximize the amount of patients served while maintaining a high level of quality and safety. | 8/10/2019 |
| 14380 | Renaissance Lakewood, NJ Manufacturing Coordinator HS Diplomga/GED Exp: Entry Level |
The Manufacturing Coordinator supports the Process Supervisor in the daily activities of union and non-union personnel in the filling and packaging of sterile and specialty pharmaceutical products in compliance with FDA regulations and cGMP guidelines. Responsible for the proper operation of all production activities assigned such as scheduling and training. This includes but is not limited to: preparing, staffing, and operating production line and safety. This is a swing shift position from 10:30 am to 7:00 pm. | 8/10/2019 |
| 14381 | Repligen Rancho Domiguez, CA Assembler I HS Diplomga/GED Exp: 0-1 years production/manufacturing |
This assembly position performs a wide variety of fiber assembly, filtration product assembly or sub-assemblies. Determines and/or follows methods and sequence of operations in performing fiber bundling, filter potting, filter welding, fitting on assembly units and packaging. The employee also works as a team member in whatever capacity and job function is required to deliver a quality product to our customer in a timely fashion. | 8/10/2019 |
| 14382 | PTC Therapeutics Bridgewater, MA Associate Scientist I, Downstream Process Dev - Gene Therapy MS in chemical/biochemical engineering or biochemistry Exp: 1 or more years in gene process development |
Associate Scientist I, Downstream Process Development (PD) – Gene Therapy actively contributes to the execution of downstream process development activities for gene therapy vector production. This includes, but may not be limited to, cell and virus culture product purification and downstream Design Of Experiment (DOE) execution. This individual executes scale-up studies from pilot through full clinical and commercial scale and interacts extensively with upstream Process Development, Analytical Development and Manufacturing personnel to deliver high-quality and robust downstream processes in a regulated environment. | 8/9/2019 |
| 14383 | Pulmatrix Lexington, MA Engineering Associate BS/BA or MS in chemical/biomedial engineering or related Exp: 1-5 years in biotech/pharma |
We are seeking a highly motivated engineer to join the Pharmaceutical Development group supporting process development for respiratory drug products. Support development and optimization of engineered particle inhaled dosage forms. Specific methods may include bench and pilot-scale spray drying. Perform physicochemical property and aerosol performance characterization of solid-based inhalation dosage forms | 8/9/2019 |
| 14384 | Purdue Coventry, RI R_Chemical Technician HS Diplomga/GED Exp: 0-2 years |
Safely operate all equipment according to procedure and regulations at all times. Must follow all SOPs’ & batch records as written and report all exceptions according to procedure. Maintain good housekeeping within the facility. Perform incidental and preventive maintenance and assist maintenance personnel in related activities. Transport materials using manual and power assisted vehicles within the interior and grounds of the site. Powered vehicle certification required. Assist materials management in related activities as required. | 8/9/2019 |
| 14385 | Purdue Coventry, RI R_ Quality Specialist I BS/MS Exp: 1 or more year in pharma |
Analyze raw materials, in-process, and finished products assuring compliance with company standards and applicable government regulations. Work closely with R&D analytical development to ensure a smooth transfer of methods. Perform qualitative and quantitative testing on routine and non-routine samples using technique analytical equipment to highly sophisticated and automated instrumentation. | 8/9/2019 |
| 14386 | Purigen Biosystems Pleasanton, CA Research Associate I/II BS in molecular biology/biology/biochemistry, etc. Exp: 1-3 years in biotech |
The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. Execute new and standard protocols for performance testing of Purigen’s custom Sample Preparation platform, including instrumentation and microfluidic chip prototypes | 8/9/2019 |
| 14387 | Pyramid Labs Costa Mesa, CA Manufacturing Technician HS Diplomga/GED Exp: 1 or more years in GMP |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. | 8/9/2019 |
| 14388 | Qiagen Germantown, MD Technical Associate - Kit Assembly Operations HS Diplomga/GED Exp: 1-3 years work experience |
The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. Responsible for Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. | 8/9/2019 |
| 14389 | QPS Newark, DE Associate Scientist I - Bioanalytical BS in chemistry/biochemistry/pharmacology Exp: 0-2 years |
An Associate Scientist in our Bioanalytical department will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. Perform routine lab operations, such as sample extraction, preparing reagents, operating automatic liquid handling equipment, pipetting, weighing, monitoring, and recording, in a neat/clean manner | 8/9/2019 |
| 14390 | QPS Fargo, ND Associate I, QC BS in sciences Exp: 0-1 years in regulatory environment |
Based in Fargo, ND, this staff member will be key in ensuring that all data produced by DTRL is documented in an accurate, complete, and timely manner. Review all study documentation for accuracy and completeness. Monitor data and documentation on an ongoing basis, and prepare QC audit reports of findings. Inspect study documentation for evidence of non-compliance with protocols, SOPs or applicable regulations. Maintain records and documentation related to laboratory systems in an organized fashion | 8/9/2019 |
| 14391 | QPS Newark, DE Associate I, Sample Coordination HS Diplomga/GED Exp: 1 or more years working experience |
This junior level associate is a key member of QPS’ DMPK lab support team, ensuring that client samples and other controlled materials are received, stored, distributed, tracked and returned safely, securely, confidentially and without loss or damage. This role requires comfort with computer systems and databases, and requires independence, attention to detail, organization, and juggling multiple tasks. | 8/9/2019 |
| 14392 | QPS Newark, DE Associate Scientist I BS in biochemistry/immunology/medical tech/biology or related Exp: 0-2 years |
The Translational Medicine (TLM) department of QPS is comprised of four laboratory operations units: Biomarker Analysis (BMA), Gene & Sequence Analysis (GSA), Immunobioanalysis (IBA), and Protein Mass Spec Analysis (PMA). An Associate Scientist in any of these units will be a fully-supervised trainee, responsible for gaining mastery of GCP and GDP, conducting assigned studies according to study protocols, and recording study results and observations. | 8/9/2019 |
| 14393 | Quanterix Billerica, MA Quality Control Analyst (Contract) BS in chemistry/biochemistry/biology Exp: 0-3 years in med devices/pharma/quality |
This position will be part of our Quality Control team, responsible for a variety of activities including incoming raw material inspection and release and Bulk Reagent/Assay Kit Inspection in accordance with current Good Manufacturing Practices (cGMPs). | 8/9/2019 |
| 14394 | Quanterix Billerica, MA Manufacturing Associate I (Contract) BS in Chemistry, Biology or related Life Sciences Exp: 0-2 years in manufacturing |
This role spans a broad range of activities within the manufacturing operations team at Quanterix. In the role, process responsibilities range from complex protein conjugations to diluent formulation to support a diverse assay menu. This is a Contract to Hire position. | 8/9/2019 |
| 14395 | Quanterix Billerica, MA Kitting Technician (Contract) HS Diplomga/GED Exp: 0-2 years in distribution/manufacturing |
This role spans a broad range of activities within the kitting team at Quanterix. In the role, process responsibilities include kitting, labeling and inventory activities to support a diverse assay menu. | 8/9/2019 |
| 14396 | Quick Biology Pasadena, CA Research Associate MS in biochemistry, molecular biology, biology Exp: 1-4 years |
We are seeking a Research Associate I to perform sample preparation, RNA/DNA extraction, QC/QA, sequencing library construction and Illumina Hiseq sequencer operation in our sequencing team. The successful candidate should have knowledge of next-generation sequencing using the Illumina platform. The successful candidate should work somewhat independently to conduct laboratory experiments on NGS projects within well-defined guidelines; Ability to independently design and execute SOPs to meet project goals is essential. | 8/9/2019 |
| 14397 | RB Parsippany, NJ Performance Marketing Analyst BS/BA or MS in chemical/biomedial engineering or related Exp: 1+ years working in media |
Activation practitioner with experience in the media/search marketplace, who is eager to have immediate impact on RB E-Business team in its activation and optimization practice. Energized by the development of data architectures to drive performance along with executing dashboards that drive clear analysis and insights on in-market media results. Eager to create meaningful vendor partnerships & act as daily trader within self-service media platforms. | 8/9/2019 |
| 14398 | RB Hillsborough, NJ Jr Quality Engineer BS in engineering sciences Exp: 1-2 years in QA |
The primary responsibilities of the Jr. Quality Engineer are to actively support Quality and Operations Packaging & Filling Processes, identify and implement process improvement opportunities, and support New Product Development (NPD)/Existing Product Development (EPD). This position is responsible for assuring Quality of products “On Shelf” and improving Consumer Experience. Duties include developing, revising, improving Quality System and related SOPs, Control Plans, and Work Instructions, as well as performing materials sampling/testing – routine lab testing is an integral part of this position. | 8/9/2019 |
| 14399 | RB Salt Lake City, UT Logistics Associate HS Diplomga/GED Exp: 0-2 years |
The Logistics Associate operates powered Lift Truck equipment to load, unload and move products, materials and equipment. This position works as a fully participating and effective member of a “Self-Managed” Logistics Team responsible to deliver World Class results in the key areas of Quality, Safety, Customer Service and Cost. | 8/9/2019 |
| 14400 | RB Montvale, NJ R&D Operations Assistant NA, Hygiene Home BS/BA in related sciences Exp: 0-2 years |
The R&D Operations Assistant will work with technical product development on key projects for the R&D team. Direct and conduct routine evaluation of existing commercial products, including performance and stability testing and claim support. Conduct evaluation of first production samples for new product launches, including performance and stability testing. Maintain appropriate level of communications with select Marketing and Supply personnel to accomplish objectives. | 8/9/2019 |
| 14401 | RB St. Peters, MO Associate Packaging Engineer BS in packaging Engineer Exp: 0-2 years |
The Associate Packaging Engineer is responsible for the package development of new and existing products to support launches and to improve gross margin. Design and develop packaging for existing products to support launches. Design and develop Customer Manufacturing offerings which include Warehouse Club and promotional SKUs. Aggressively drive and identify gross margin improvement projects through the optimization of primary and secondary package design / re-design. | 8/9/2019 |
| 14402 | RB Montvale, NJ R&D Assistant, Laundry and Disinfection BS in sciences Exp: 1 or more years |
The R&D Assistant will apply technical knowledge working toward multiple project goals and objectives within established timelines. Key requirement for the incumbent will be prior experience working with Laundry products. Prepare various formulations in the lab and conduct performance evaluations (e.g. cleansing ability, fragrance) on formula applications. Conduct chemical and physical evaluations on various formula applications, e.g. stability testing including viscosity, pH, pump testing, pack weight, UV testing, packaging compatibility testing | 8/9/2019 |
| 14403 | RB Montvale, NJ R&D Operations Assistant NA, Hygiene Home BS/BA in related sciences Exp: 0-2 years |
The R&D Operations Assistant will work with technical product development on key projects for the R&D team. Direct and conduct routine evaluation of existing commercial products, including performance and stability testing and claim support. Conduct evaluation of first production samples for new product launches, including performance and stability testing. Maintain appropriate level of communications with select Marketing and Supply personnel to accomplish objectives. | 8/9/2019 |
| 14404 | Regeneron Tarrytown, NY R&D Associate, VelocImmune (VI) Next MS in molecular biology/biochemistry Exp: 0 years |
We are seeking a motivated, highly organized researcher to support our investigations of new antibody and cell-based therapies. Independently and as a team, conduct and support experiments. Investigating and develop new methodologies and technologies in molecular biology and biological therapeutics. Characterization of mice via NGS (next-generation sequencing) and flow cytometry-based phenotyping. Design, construct, and test DNA vectors, viral vectors, and cell-lines for in vitro and in vivo studies of candidate biologicals. | 8/9/2019 |
| 14405 | Regeneron Tarrytown, NY R&D Associate (Immunology/Autoimmune Diseases) BS/MS Exp: 0-2 years |
We are seeking a motivated R&D associate to join the VI-Next group to support our effort in developing new in vivo disease models and testing the therapeutic potential of new candidate molecules. The new recruit will contribute to project advancement by performing in vivo work and in vitro assays such as cell culture, immunoassay and flow cytometry. | 8/9/2019 |
| 14406 | Regeneron Tarrytown, NY R&D Associate -Analytical Chemistry BS in chemistry/biochemistry Exp: 0-5 years in protein mass spectrometry |
This role will primarily be involved in developing and executing state-of-the-art mass spectrometry and its related technologies for the analytical characterization (e.g., intact mass analysis and peptide mapping) of therapeutic proteins (e.g., monoclonal and bispecific antibodies) to support drug development activities at all stages (e.g., INDs, BLAs, comparability studies, stability studies, cell line development, process development, and formulation development), with a primary focus on supporting early stage drug candidate characterization and lead candidate selection. | 8/9/2019 |
| 14407 | Regeneron Tarrytown, NY Associate Scientific Writer BS in life sciences Exp: 0-2 years supporting nonclinical/clinical development |
Provides support for the Preclinical Development department. Drafts and manages reviews for pharmacokinetics, toxicokinetics, clinical bioanalysis, clinical pharmacology, and CMC reports. In addition, drafts pharmacokinetics, toxicology, and CMC documents in support of IND and BLA submissions. Provides quality control review for regulatory documents in support of INDs and BLAs, as well as other written documents in support of development projects, as determined by management. | 8/9/2019 |
| 14408 | Regeneron Tarrytown, NY Associate QC Analyst (Bioassay, 2nd Shift) BS/BA in life sciences Exp: 0-2 years lab experience |
Summary: Performs biological analyses in a GMP environment on products, in-process materials, raw materials and stability studies in support of the company’s quality program. Performs potency testing using cell based bioassays and binding ELISA assays. Maintains cell lines using aseptic technique and good cell culture practices. Maintains laboratory supplies. | 8/9/2019 |
| 14409 | Regeneron Tarrytown, NY Cell Banking Associate BS/BA in life sciences or engineering Exp: 0-2 years cGMP experience |
Summary: Performs cGMP cell banking to support Manufacturing operations. Essential Duties and Responsibilities may include, but are not limited to, the following: Conducts scaled-down production procedures of newly prepared banks. Perfoms analysis of samples generated from lab scale studies and cell bank testing. Maintain cell banking inventory and perform vial transfers for shipment and prodcution. | 8/9/2019 |
| 14410 | RegenxBio Rockville, MD Associate Scientist, Analytical Development (Molecular Biology) BS in sciences Exp: 0-2 years industry experience |
The Analytical Development department at REGENXBIO is seeking an exceptional, highly motivated analytical scientist to join a dynamic and highly collaborative team. The individual must be a technical and scientific expert in the field of analytical sciences for biologics. The individual is responsible for developing analytical methods to support the development, manufacture and release of gene therapy products at REGENXBIO. It is required to effectively use the current available technologies and apply appropriate analytical stringency and savvy for the stage of development, and in alignment with regulatory expectations. | 8/9/2019 |
| 14411 | RegenxBio Rockville, MD Associate Scientist/Senior Associate Scientist, Upstream Process Development MS in biological sciences or engineering Exp: 1+ years |
Reporting to a Scientist/Senior Scientist, the Associate Scientist/Senior Associate Scientist will work on developing and optimizing novel cell culture processes for AAV production. Responsibilities may include routine cell culture, cell banking, process development, scale up, tech transfer for GMP production, data analysis, and authoring of technical reports and tech-transfer documents. Furthermore, this individual is expected to work independently on assigned tasks/projects, provide insight to improve processes, and communicate results in a timely manner. | 8/9/2019 |
| 14412 | RegenxBio Rockville, MD Regulatory Affairs Associate, CMC BS/BA in biological sciences Exp: 1-3 years regulatory affairs |
Reporting directly to the Senior Director of Regulatory Affairs, the Associate of Regulatory Affairs, CMC is responsible for providing support for regulatory activities related to chemistry, manufacturing, and controls for each product development area from early development through BLA. The incumbent will also provide the organization with regulatory and scientific expertise to enable high quality and effective health authority and team communications to effectively support the product development process. | 8/9/2019 |
| 14413 | RefleXion Medical Hayward, CA Firmware Engineer MS in eletrical or computer engineering Exp: 1+ years |
The Firmware Engineer at RefleXion will have firmware responsibility for the RefleXion‘s embedded system. This engineer is expected to deliver firmware solutions for interfacing hardware resources to application programs. The engineer will work with a highly integrated team on specification, design, debug, verification and validation, CE approval, FDA submissions, and documentation control. | 8/9/2019 |
| 14414 | TE Connectivity Fuquay Varina, NC Product Engineer I AS/BS in engineering or engineering technology Exp: 1-3 years |
TE Energy business unit in Fuquay-Varina, North Carolina is seeking a Product Engineer to support both existing and new product development/improvement activities. The primary focus will be on the improvement and maintenance of existing system data (drawings, BOM’s, routings, product requirements, specifications, SWI’s, label templates, packaging requirements, etc.) necessary to the flawless operation of today’s ERP systems. However, this position interacts with every function within the company. Business acumen is fundamental. etc. | 8/6/2019 |
| 14415 | TechLab unspecified, VA Quality Assurance Officer 1 AS/BS/BA Exp: AS 1+ years, BA/BS none needed |
The Quality Assurance Officer 1 is responsible for ensuring that all TechLab® Inc. products meet the requirements of the quality system. This can include reviewing and tracking product as well as reviewing documentationto ensure it complies with regulatory standards. The Quality Assurance Officer 1 reports to the Quality Assurance Manager. etc. | 8/6/2019 |
| 14416 | Tecomet Boulder, CO Machine Operator - entry HS diploma or equivalent Exp: 0-2 years |
Under the direction of the Director, Operations, maintains the Quality system as directed. Majority of tasks performed under the supervision of an experienced machinist or the Production Manager. Takes direction to learn basic machine operation, setup and maintenance. Duties and tasks are simple and repetitive. etc. | 8/6/2019 |
| 14417 | Tecomet Warsaw, IN CNC Machinist 1- Mills or Lathes-2nd or 3rd shift HS diploma or equivalent Exp: 0.5-3 years |
This positions requires basic CNC machining knowledge in order to produce machined parts to specification in an efficient and timely manner. This job requires skills to achieve metrics set forth within a specified work group or team. This is accomplished by maintaining Tecomet’s principles of Safety, Quality, Customer Satisfaction and Innovation. etc. | 8/6/2019 |
| 14418 | Tecomet Kenosha, WI Instrument Maker, Med Device (Hand Finisher/ Assembler)- TecoGR HS diploma or equivalent Exp: 1-5 years |
This position is responsible for prioritizing work orders and assigning the necessary resources to finish components to meet manufacturing schedules. PRINCIPAL RESPONSIBILITES: Work may include bending, blasting, tumbling, buffing, polishing, grinding, marking, electro polishing, cleaning and hand filing. Prioritize work orders with other cell members to ensure production schedules are maintained. Perform transactions in company system. etc. | 8/6/2019 |
| 14419 | Tecomet Kenosha, WI Milling Waterspider (Job/Material Kitter) HS diploma or equivalent Exp: 1+ years |
Responsible for kitting orders for Milling, Turning, and Swiss machining centers, providing all tooling, gaging, fixturing, vise jaws and material required to set up jobs, and staging kits before the start of a given job. PRINCIPAL DUTIES AND RESPONSIBILITES: Ensure shop paperwork is complete and accurate before starting kitting the job. Issue tooling from Robo Crib and set up necessary tools following machining set up sheets ensuring all tools are sharp and are in good condition. Issue gaging From Robo Crib using in process and FAI paperwork. etc. | 8/6/2019 |
| 14420 | Tecomet Kenosha, WI Utility Operator, 2nd Operations, Level 1 HS diploma or equivalent Exp: None |
Produce a quality product per print as assigned, with average supervision. Person must rely on experience and judgment to accomplish goals with above average degree of independence and initiative to complete job requirements in a timely manner. Must understand the company’s organization and overall policies. PRINCIPAL RESPONSIBILITES: Performs assigned jobs in, glass bead, clean/pack, and deflashing, as needed. Performs in-process quality checks on all work performed. Adheres to general safety rules, manufacturing procedures and work instructions, company policies and procedures, Good Manufacturing Practices (GMP) and FDA regulations. etc. | 8/6/2019 |
| 14421 | Tedor Pharma Cumberland, RI Production Technician HS diploma or equivalent Exp: 1-2 years |
The Production Technician position performs all tasks involved in the pharmaceutical process following cGMP’s and SOP’s such as wet granulation, dry granulation, tablet compression, encapsulation, tablet coating, packaging and finished product, put product on stability. The position follows standard work methods and practices safe work habits to ensure production is as efficient and safe as possible. etc. | 8/6/2019 |
| 14422 | Teligent Buena, NJ 2nd Shift Compounder AA/AS Exp: 1 year |
Perform functions relating to the processing of Topical products (creams, ointments, lotions, solutions) ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements, and in conjunction with all Standard Operating Procedures (SOPs). Perform functions relating to the cleaning and sanitization of compounding process equipment and compounding facility to facilitate GMP compliance, quality, safety, and schedule attainment. Follow standard operating procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. Apply skills and knowledge to recognize process issues and to increase efficiency, throughput and quality. Responsible for the safe and efficient execution of job duties. etc. | 8/6/2019 |
| 14423 | Teligent Buena, NJ QC Chemist I BS in chemistry or related Exp: 0-3 years |
Provide accurate and timely testing of raw materials, finished product and/or stability samples as assigned. Ensure the safety and reliability of products produced in compliance with quality and regulatory requirements. Essential Responsibilities: Perform quality control testing on raw materials, finished product, pre-approval and commercial stability samples as assigned by the supervisor. Wet and Physical chemistry techniques including but not limited to: Karl Fisher, Viscosity, Microscopy, pH, specific gravity, IR, Specific Rotation and wet chemistry. etc. | 8/6/2019 |
| 14424 | Tempus St. Louis, MO Account Associate - St. Louis BS in biology, life science, business, or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). etc. | 8/6/2019 |
| 14425 | Tenaya Therapeutics San Francisco, CA Research Associate I -iPS Cell Culture, Drug Discovery BS/MS in biology, biochemistry, or related Exp: 0-2 years |
Key Responsibilities: Maintain human iPSC cultures and differentiate to cells of the cardiovascular lineage. Perform a diverse range of cell-based assays to discover and characterize lead therapeutic molecules for heart failure. Oversee aspects of maintaining the cell culture lab, including preparing reagents, helping with room upkeep, and restocking. Execute a range of experiments using molecular biology techniques including plasmid design, nucleic acid and protein isolation, PCR, cloning, virus preparation, and immune assays. Generate SOP protocols when required for new procedures. Regularly present scientific findings in internal scientific discussions and meetings. | 8/6/2019 |
| 14426 | TeraRecon Durham, NC Technical Support Specialist BS in computer engineering or related Exp: 1+ years |
We are seeking a Technical Support Specialist with a broad set of skills in HealthCare IT systems in a highly regulated environment. The position is in our Durham Office in North Carolina. Responsibilities: Provide technical support to customers via phone, email or chat utilizing remote access tools provided by TeraRecon. Actively Monitor customer systems for failures/issues and follow-up on those remotely. Analyze and resolve customer service issues associated with TeraRecon products running on Windows Workstations and Windows Server Operating Systems. etc. | 8/6/2019 |
| 14427 | TeraRecon unspecified, Jr. Technical Support Specialist AS/BS in engineering Exp: 1+ years |
We are seeking a Junior Technical Support Specialist with an understanding of Healthcare IT systems and basic computer hardware software knowledge. Responsibilities: Provide first line of technical support to customers via phone, email or chat utilizing remote access tools provided by TeraRecon. Analyze and resolve basic customer service issues associated with TeraRecon products running on Windows Workstations and Windows Server Operating Systems. Prompt escalation of customer product issues in a timely manner for analysis and further action by higher level of support. etc. | 8/6/2019 |
| 14428 | Tergus Pharma unspecified, Scientist 1, IVPT BS/MS in chemistry, biology, pharmaceutical sciences, or related Exp: 1+ years |
Develop and validate skin permeation and/or LC-MS/MS analytical test methods with guidance from senior laboratory personnel. Carry out laboratory work as directed by senior laboratory personnel. Conduct routine analytical experiments using established analytical methods and procedures. Assist with assembling data packs. etc. | 8/6/2019 |
| 14429 | Tergus Pharma unspecified, Associate Scientist, IVPT AS/BS in chemistry, biology, pharmaceutical sciences, or related Exp: 0+ years |
Job Purpose: This laboratory-based position will support the analysis of semi-solid drug products, with a focus on performing Skin permeation/IVPT experiments. Summary of Key Responsibilities: Conduct routine analytical experiments using established skin permeation methods and procedures. Troubleshoot and maintain analytical instrumentation for maximizing uptime. Coordinate instrumentation to facilitate maximum use of existing equipment. Maintain a GxP-compliant analytical laboratory and safe laboratory working environment. | 8/6/2019 |
| 14430 | Terumo Medical Elkton, MD Engineer I - Test and Evaluation BS in engineering Exp: 0-3 years |
Job Summary: The Test & Evaluation Engineer 1 is responsible for providing engineering support for planning and execution of NPD test and evaluation activities. Testing activities may include new product concept testing, competitive benchmarking, marketing claim substantiation, formal design verification testing (including accelerated and real time aging), usability testing, and root cause analyses. The Test & Evaluation Engineer 1 may serve as an extended project team member and will typically coordinate with marketers, development engineers, process engineers, manufacturing and quality engineers. Job Details: 1. Coordinate with engineers and marketers to define and develop test methods, fixtures, test protocols and test plans to achieve the defined testing objective(s). etc. | 8/6/2019 |
| 14431 | Terumo Medical Elkton, MD NPD Test & Evaluation Technician HS diploma or equivalent Exp: 1-5 years |
Job Summary: The NPD Test & Evaluation Test Technician position is responsible for the preparation and testing of pre-production devices to support the product development process. The position is also responsible for testing support of competitor product evaluations for marketing information. Assisting in preparing the lab for simulated clinical evaluations and new product pilot lines is also included in the position. An additional responsibility is supporting the acquisition, calibration and validation of lab equipment. Job Details: 1. Associate is responsible to follow requirements of TMC Quality System; including but not limited to: document/data control, compliance with procedures, and change control practices. 2. Perform basic product testing on prototype, pre-production, and/ or final design products. etc. | 8/6/2019 |
| 14432 | Terumo Medical Somerset, NJ Customer Care Representative-2nd shift BA/BS Exp: 1+ years |
Customer Care Representative (CCR) strives to provide the absolute best customer experience on a daily basis. Responsible for managing all customer requests pertaining to product orders, returns, or general inquiries with a focus on customer satisfaction. CCR work in a fast paced team environment to support Terumo’s Interventional Systems, Medical Products, and Global Pharmaceutical Solutions businesses. Working in a high volume call center, CCR must be willing to help drive process improvement, in an effort to always exceed customer’s expectations. The Customer Service Team has a proven track record for upward movement for high performing individuals. etc. | 8/6/2019 |
| 14433 | Terumo Medical Elkton, MD Assembler II - 1st shift (8 am - 4:30 pm) HS diploma or equivalent Exp: 1-2 years |
Job Summary: Performs manual and/or repetitive job duties which may include inspecting, packing, and assembling of product. Job Details: 1. Manually pack product into proper shelf packs/cases/shippers/bags, etc. 2. Ability to inspect both visually and functional aspects of product. 3. Ability to assemble product as required; may need use of hand tools. 4. May include some equipment operation. etc. | 8/6/2019 |
| 14434 | Terumo Medical Somerset, NJ Clinical Research Associate (CRA) BS in life science Exp: 1-3 years |
Job Summary: PURPOSE: Ensure clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements by engaging with assigned sites. JOB DETAILS: • Perform site selection, start-up/regulatory, initiation, monitoring and close out visits in accordance with contracted scope of work, using good clinical practices, applicable regulations, SOPs and work instructions. • Complete appropriate therapeutic, protocol and clinical research training to perform job duties. • Administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues. etc. | 8/6/2019 |
| 14435 | Teva Pharmaceuticals Salt Lake City, UT Pharmaceutical Technology Specialist I BS/MS Exp: 1-2 years |
Under general supervision, the Pharm Tech Specialist I determines the critical aspects of manufacturing equipment with regard to product and process, and writes protocols and other records related test results. Prepares final reports that identify the results of protocol testing and the conditions of release. Assists in conducting efficiency studies and in the identification of process improvement opportunities. Participates in project coordination activities. etc. | 8/6/2019 |
| 14436 | Teva Pharmaceuticals North Wales, PA Material Handler I - 2nd Shift HS diploma or equivalent Exp: 6 months |
Under general supervision, works in one or more various work group areas, as assigned – inbound, outbound, picking, packing, sorter, replenishments, inventory control, DEA control cage & vault and refrigerated storage areas. Time spent in any area may vary by day-to-day business requirements. Essential Duties & Responsibilities: Performs various functions related to receiving, processing, shipping customer orders and managing inventory: Utilizes radio frequency (RF) system and operates fork-lift to receive and put-away inbound (IB) receipts - includes physically breaking down and creating optimal sized pallets prior to put-away into inventory. Utilizes RF system and operates fork-lift to move inventory throughout the warehouse for the purpose of managing inventory and replenishing picking locations. etc. | 8/6/2019 |
| 14437 | Teva Pharmaceuticals Grand Island, NY Receptionist HS diploma or equivalent Exp: 1-3 years |
Supports general office receptionist duties to include performing administrative office-support service tasks. Responsible for properly answering and routing incoming calls and performs general business office operations by providing various administrative support activities as a generalist or in a combination of the Disciplines in Administrative Services Function. Must have prior incoming call center service, receptionist or office assistance experience. Entry to mid-level role acquiring basic administrative skills required to perform day-to-day operations. Self-starter, who is capable of working well independently with minimal supervision. Good communication skills, both written and verbal. Strong attention to detail. Professional demeanor. etc. | 8/6/2019 |
| 14438 | Teva Pharmaceuticals New Britain, PA Material Handler I - 3rd Shift HS diploma or equivalent Exp: 6 months |
Under general supervision, works in one or more various work group areas, as assigned – inbound, outbound, picking, packing, sorter, replenishments, inventory control, DEA control cage & vault and refrigerated storage areas. Time spent in any area may vary by day-to-day business requirements. Essential Duties & Responsibilities: Performs various functions related to receiving, processing, shipping customer orders and managing inventory: Utilizes radio frequency (RF) system and operates fork-lift to receive and put-away inbound (IB) receipts - includes physically breaking down and creating optimal sized pallets prior to put-away into inventory. etc. | 8/6/2019 |
| 14439 | Teva Pharmaceuticals Parsippany, NJ Accounts Receivable Specialist AA/AS Exp: 1+ years |
The AR Specialist on the Cash & Manual Transactions Team is responsible for providing financial, administrative and transactional processing services and expertise to ensure effective, efficient and accurate financial and administrative operations for multiple operating units within the Global Teva organization. The Accounts Receivable Specialist is a key support person for the department who can meet deadlines, manage workload based on critical needs, and be able to provide extensive support across a variety of areas. Due to business fluctuations, the below duties and responsibilities can be shared or done exclusively by a given individual with this position title. The AR Specialist must work within established policies and procedures in compliance of SOX regulation. etc. | 8/6/2019 |
| 14440 | Teva Pharmaceuticals North Wales, PA Material Handler I - 1st Shift HS diploma or equivalent Exp: 6 months |
Under general supervision, works in one or more various work group areas, as assigned – inbound, outbound, picking, packing, sorter, replenishments, inventory control, DEA control cage & vault and refrigerated storage areas. Time spent in any area may vary by day-to-day business requirements. Essential Duties & Responsibilities: Performs various functions related to receiving, processing, shipping customer orders and managing inventory: Utilizes radio frequency (RF) system and operates fork-lift to receive and put-away inbound (IB) receipts - includes physically breaking down and creating optimal sized pallets prior to put-away into inventory. Utilizes RF system and operates fork-lift to move inventory throughout the warehouse for the purpose of managing inventory and replenishing picking locations. etc. | 8/6/2019 |
| 14441 | Teva Pharmaceuticals Salt Lake City, UT Quality Control Analyst I BS Exp: 1 year |
Under general supervision, performs cGMP laboratory analyses of Finished products and in process materials. Performs stability testing for Finished products. Performs maintenance and calibration of analytical instruments. Essential Functions Include: Carries out responsibilities in accordance with the organization’s policies, procedures and state, federal and local laws. Operates general analytical instruments during the testing of finished products using HPLC, UPLC, GC-FID, UV-VIS, FTIR, automatic titrators, Dissolution Apparatus, particle size analyzer, Instron, Densitometer, Rheometer, viscometer (LV/RV/Cone and Plate), pH meter and analytical balance. etc. | 8/6/2019 |
| 14442 | The Ritedose Corporation Columbia, SC Product Formulation Technician HS diploma or equivalent Exp: 0-2 years |
The Product Formulation Technician is responsible for operating compounding equipment and may be required to work in both the Commercial formulation area, as well as, the Development formulation area. Responsibilities also include following necessary methods and procedures to produce a functional compounding process. The Product Formulation Technician ensures that documentation and activities in the compounding area are compliant with any applicable regulations. etc. | 8/6/2019 |
| 14443 | Theragenics Corporation Norcross, GA Assembly Technicians - First and Second Shift HS diploma or equivalent Exp: 1+ years |
The Assembly Technician will perform basic assembly operations for medical device assembly of a variety of suture products in a clean room environment. Essential Duties and Responsibilities: Set up the work station for each new production lot. Perform machine operations for surgical suture assembly according to standard operating procedures, specifications and work instructions. Follow quality and safety procedures. etc. | 8/6/2019 |
| 14444 | ThermoFisher Scientific Rockford, IL Packaging Technician I (2nd Shift) HS diploma or equivalent Exp: 4+ months |
General assembly of Thermo Fisher products. This includes processing work orders to build kits, label products, print and fold instruction booklets, and assist other Packaging Associates with completing work orders. What will you do? Set up and operate packaging and labeling equipment. Process label work orders for manufacturing departments, travelers, and any other documents that require printing. Print out Batch Record Sheets, if applicable Print labels using the approved label software Create and print spec sheets and CofA’s. Get the appropriate approvals before printing. Process jobs utilizing less complex equipment – pipetters, shrink wrapping, automated labelers, etc. | 8/6/2019 |
| 14445 | ThermoFisher Scientific Fair Lawn, NJ QC Technician AS/BS in chemistry or biochemistry Exp: 0-1 year laboratory experience |
Prepare reagent/standard in accordance with ACS, USP and other outlined company procedures. Key Responsibilities: Responsible to keep lab area clean in accordance with 5S/housekeeping standards. Wash glassware as needed to minimize dirty glassware in the lab. Coordinate with outside labs to ensure prompt delivery of results. Responsible to check operation, function and calibration of lab equipment. Conduct verification of equipment such as pH meter, balances on daily basis. Ensure lab has required reagent, chemical and standard that are within expiration date. | 8/6/2019 |
| 14446 | ThermoFisher Scientific Austin, TX Scientist I, Formulation, 1st shift BS in biochemistry or related Exp: 0-5 years |
Animal Health Reagents manufacturing team at Thermo Fisher Scientific (Austin) is responsible for the production and testing of various reagents for qPCR and sample preparation applications including master mixes, nucleic acid purification, and internal positive controls for use in various workflows such as veterinary diagnostics, USDA-certified, and custom products. Our team is dynamic and fast paced, relying on teamwork, multitasking and communication within the team and the larger organization. We are seeking an energetic individual with strong communication, technical, and operational skills to join our team as Scientist I, Formulation. etc. | 8/6/2019 |
| 14447 | ThermoFisher Scientific Rockford, IL Packaging Technician I (1st Shift) HS diploma or equivalent Exp: 4+ months |
Entry level position into the Packaging/ Labeling department. The associate will develop mandatory skills for continued employment at Thermo Fisher. These skills include learning paperwork, basic packaging/ labeling skills, and demonstration of an excellent work ethic, ability to grow with the team, communication skills, and ability to follow direction. Excelling in this position will allow for upward mobility within the department. etc. | 8/6/2019 |
| 14448 | ThermoFisher Scientific Breinigsville, PA Distribution Study Associate HS diploma or equivalent Exp: 1-2 years |
Responsible for timely order entry of clinical study materials and clinical supplies to distribution facilities, customer affiliates and/or investigator sites globally. What will you do? Deciphers customer requests and enters into the Global Project Management (GPM) System. Accurately enters data in GPM and verifies other DSA’s work within the system. Contacts both internal and external clients with issues that may arise and answers general questions regarding shipments. Identifies discrepancies and uses problem solving abilities. Reports reasons for discrepancies to Team Leader. | 8/6/2019 |
| 14449 | Tolmar Windsor, CO Packaging Development Engineer I BS in packaging engineering or related Exp: 1+ years |
Under general supervision, develops the packaging components and packaging requirements for existing commercial products and for development projects. Develops, maintains and monitors packaging components to ensure compliance with Quality, Safety, Manufacturing and Regulatory guidelines and procedures. Conducts testing activities that influence selection of primary, secondary and tertiary packaging components. Essential Duties & Responsibilities: Work with project team to identify, select, and test primary, secondary and tertiary packaging components. etc. | 8/6/2019 |
| 14450 | Teligent Buena, NJ Analytical Scientist BS in organic chemistry or related Exp: 1-3 years |
Assist with providing high quality analytical method development and validation in a GMP environment. Support new product development through analysis of innovator samples and R&D formulations. Essential Responsibilities: Participate in the development and validation of analytical methods and improvement of existing ones to support all stages of drug development from drug substance characterization through formulations and process development and ANDA submission of oral and topical products. etc. | 8/6/2019 |
| 14451 | Tempus Philadelphia, PA Account Associate - Philadelphia BS in biology, life science, business, or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). etc. | 8/6/2019 |
| 14452 | Tempus Nashville, TN Account Associate - Nashville BS in biology, life science, business, or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). etc. | 8/6/2019 |
| 14453 | Tempus Washington, DC Accout Associate - DC BS in biology, life science, business, or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). etc. | 8/6/2019 |
| 14454 | Prescos San Diego , CA Vivarium Assistant HS Diploma/GED Exp: 0-1 years in animal husbandry |
We are looking for a full-time Vivarium Assistant to perform husbandry tasks such as thechanging and cleaning of animal cages, feeding/watering of animals, and the sanitation/ cleaning of the animal facility. | 8/5/2019 |
| 14455 | Progenity Ann Arbor, MI Molecular Technologist Assay I BS/BA in medical technology or life sciences Exp: 1 or more year in clinical lab |
This is an entry level position for the Molecular Assay testing laboratory. The Molecular Technologist – Assay I works independently but closely with the technical staff, leads, supervisors, and other departments to perform routine testing within the Progenity laboratory. The Molecular Technologist – Assay I independently executes routine tasks as trained. The Molecular Technologist – Assay I may be asked to participate in processes for clinical research or development projects as needed. This position reports to the Laboratory Assay Supervisor. | 8/5/2019 |
| 14456 | ProSciento San Diego , CA PT Pharmacy Technician HS Diplomga/GED Exp: 1 or more year as pharma technician |
This position is responsible for performing pharmaceutical related functions in compliance with state and federal regulations, protocol specific requirements, and the Company’s values, policies, and procedures under the direction of the Pharmaceutical Services Supervisor. Receive, label, store, organize, and return/destroy study medications for clinical trials. Prepare and update all drug inventory logs and ensure logs are current with all clinical trial drug preparation schedules. | 8/5/2019 |
| 14457 | ProSciento San Diego , CA Clinical Research Coordinator BS/BA in sciences/medicine Exp: 1 or more year clinical research |
The Clinical Research Coordinator will be the main operational interface with study subjects during the conduct of a study. The CRC will participate in and manage all administrative aspects of clinical trials under the direction and supervision of the Manager, Clinical Study Management. The ideal candidate will have experience as a CRC at a clinical research site working in the fields of diabetes, metabolism, or endocrinology. Performs duties in accordance with ProSciento’s values, policies, and procedures. | 8/5/2019 |
| 14458 | Mission Pharmacal Boerne, TX Plant Sanitation Trainee HS Diplomga/GED Exp: 1 or more years |
One year general work experience or equivalent education. Ability to read and understand documents such as policy manuals, safety rules, operating and maintenance instructions, and procedure manuals; Ability to write routine reports and correspondence. Ability to effectively communicate information and respond to questions in person-to-person and small group situations with customers, clients, general public and other employees of the organization. | 8/5/2019 |
| 14459 | Mission Pharmacal Boerne, TX Product Handler Trainee (Day) HS Diplomga/GED Exp: 1 or more years |
Mission Pharmacal Company, a pharmaceutical manufacturing company, is seeking an energetic Product Handler Trainee to join our team in Boerne, TX. Responsibilities include performing assembly/production, warehouse/receiving, distribution or manufacturing functions. | 8/5/2019 |
| 14460 | Protagonist Therapeutics Newark, CA Clinical Trial Assistant BS/BA Exp: 1+ years as a CTA in Biotech/Pharma or CRO |
Experience across multiple therapeutic areas e.g. gastrointestinal, hematology preferred. Experience and understanding of study start-up processes, including Trial Master File and associated document management procedures. Good overall understanding of the major areas within clinical operations. Excellent communication and interpersonal skills, along with attention to detail and organizational skills. Strong written and spoken English. Ability to collaborate, problem solve and work in a small dynamic company with minimal supervision, to achieve personal and team goals. | 8/5/2019 |
| 14461 | Biotechne Minneapolis, MN Research Associate - Protein Purification BS/BA or MS in biology or related Exp: BS: 0-2 years, MS: 1-3 years |
The responsibilities of this position are to purify proteins to restock the supply of existing products and modify existing protocols for larger scale production of proteins. This position will require assistance with basic lab operations and routine guidance on how to follow SOP’s and purification methods. | 8/5/2019 |
| 14462 | Biotechne Minneapolis, MN Manufacturing Associate BS/BA or AA/AS Exp: 0-2 years |
The primary purpose of this Manufacturing Associate position is to perform manufacturing support functions. This role will require the ability to review Manufacturing DHR and perform in process quality checks throughout the day at various manufacturing lines. This includes reconciliation, kitting verification, labor collection, and coordination of scheduled activities with the Manufacturing Manager or as direction from the Manufacturing Team Leader. This position is dedicated to maintaining compliance in the manufacturing area. | 8/5/2019 |
| 14463 | Biotechne San Jose, CA Manufacturing Laboratory Technician AA Exp: 1+ year lab experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Operate and maintain cartridge fabrication process, with good manual dexterity. Perform in-process QC and record results. Microscope inspection of chips and microfluidic devices | 8/5/2019 |
| 14464 | Biotechne San Jose, CA Manufacturing Laboratory Technician HS Diploma Exp: 1+ years lab/manufacturing experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of WES cartridges for biotech products. Operate and maintain robotic and manufacturing equipment. Ability to use hand tools such as small wrenches, pliers, tweezers, etc. Perform in-process QC and record results. | 8/5/2019 |
| 14465 | Biotechne Minneapolis, MN QA Specialist BS/BA in sciences Exp: 0-2 or 2-5 years in QA in scientific field |
The responsibilities of this position are to support the Quality Assurance function within Bio-Techne through quality systems development, quality systems auditing, documentation review, and other QA functions. | 8/5/2019 |
| 14466 | PTC Therapeutics Bridgewater, NJ Associate Scientist I, Upstream Process Dev - Gene Therapy MS in chemical engineering/biological engineering Exp: 1 or more year in biologics/gene process development |
This individual executes scale-up studies from pilot through full clinical and commercial scale and interacts extensively with downstream Process Development, Analytical Development and Manufacturing personnel to deliver high-quality and robust upstream processes in a regulated environment. | 8/5/2019 |
| 14467 | Premier Research Group Research Triangle Park, NC Contract Specialist I BS/BA in business, legal studies, or life sciences Exp: 1 or more years in legal services |
The Contract Specialist is responsible for all aspects of preparation, negotiation and execution of required contractual agreements associated with an investigative site participating in a clinical study. The Contract Specialist assumes responsibility on quality deliverables throughout the conduct of the study with a concentration on Site Start Up and up to Site initiation. | 8/5/2019 |
| 14468 | Performance Validation Multiple Locations, na Level 1 Staff Validation Engineer / Specialist BS in life science/engineering Exp: Entry Level |
The Level 1 Validation Engineer/Specialist works within a small team environment to provide technical services to pharmaceutical or medical device manufacturers. Technical services may include interpreting drawings, manuals, or other technical information to develop requirement documents, developing testing documents that verify installation, and/or operation of the equipment, and execution /documentation of these testing documents. | 8/4/2019 |
| 14469 | PerkinElmer Austin, TX Associate Scientist BS/BA in life sciences Exp: 1+ year in NGS library prep |
Perform lab experiments as planned and document all observations and findings. Prepare hybridization capture NGS libraries and amplicon panel NGS libraries. Analyze and interpret data. Present experimental findings and interpretations to senior research team members. Demonstrate potential for technical proficiency and ability to collaborate with others. | 8/4/2019 |
| 14470 | PerkinElmer Waltham, MA Associate Scientific Services Specialist, Lab Technician HS Diploma/GED or AS/AA Exp: 1-2 year work experience |
The candidate will conduct laboratory maintenance procedures in compliance with established protocols and in compliance with regulatory and laboratory requirements. Maintains suite equipment including, but not limited to: incubators, water baths, and biosafety cabinets. Monitors incubator temperature, CO2 and humidity. Responsible for the cleaning, sterilization and equipment functionality. | 8/4/2019 |
| 14471 | Perrigo Allegan, MI Associate SAP Developer HS Diploma/GED Exp: 0-3 years ABAP coding |
Perrigo is looking to add an Associate SAP Developer to its team located at their North American HQ in Allegan, MI. The Associate Developer will be accountable for designing, developing, testing, and implementing SAP-based applications written primarily in ABAP. The Associate Developer will also provide day-to-day applications support of SAP and other integrated systems, including quick and efficient problem analyses and resolution. | 8/4/2019 |
| 14472 | Pfizer St. Louis, MO Associate Scientist, Upstream Process Development BS/BA in biotechnology/biological sciences Exp: 0-2 years industrial experience |
An Associate Scientist (R1) position is available in the Process Development group of Bioprocess R&D. The successful applicant will join a team of scientists and engineers focused on developing and optimizing microbial/ mammalian cell culture processes for recombinant proteins and biologics for early- and late-phase clinical trials. In this role you will be responsible for designing and executing bioreactor experiments in bench-top bioreactors and associated scale-down equipment with the goal of developing robust, scalable, and high productivity processes that produce therapeutic proteins with the appropriate product quality to treat human disease. | 8/4/2019 |
| 14473 | Pfizer Rocky Mount, NC Associate Procurement, Indirect Spend BS/BA in business/supply chain/engineering Exp: 1-4 years in procurement or finance |
This role is responsible for delivering value, including year on year cost savings, within the Indirect categories within Market/Site, across all Business Unit’s and Divisions as applicable. The buyer role provides operational support to the procurement team, including data analysis and reporting, market intelligence gathering, and project tracking. This role also acts as a liaison with Category Strategy Managers (CSM) to support the execution of Market/Site, and where agreed, Regional category strategies through participation on cross-functional teams | 8/4/2019 |
| 14474 | Pfizer Andover, MA Production Engineer I BS in engineering Exp: 0-2 years, co-op/internship experience |
Provide engineering and technical support related to the operation, maintenance, installation, startup/commissioning, testing, and qualification of process and automated equipment and systems within a biopharmaceutical manufacturing facility. This may include production equipment such as bioreactors, fermentors, ultrafiltration skids, Clean – In – Place (CIP) skids, and other support equipment. | 8/4/2019 |
| 14475 | Platelet Biogenesis Cambridge, MA Research Associate, Gene Editing BS/MS in biology, immunology, molecular biology Exp: 1-3 years lab experience |
The successful Research Associate will join our Designer Platelet Team, working directly on genetic engineering of pluripotent stem cells as part of our drug delivery platform. Optimizing standard operating procedures associated with platelet loading of small-molecule and biologic drugs. Developing protocols for transgene delivery in iPSCs | 8/4/2019 |
| 14476 | PMI Biopharma Solutions Nashville, TN Engineering Maintenance Technician I, MSAT HS Diploma/GED Exp: 1-2 years in manufacturing |
Reporting to the Supervisor of Engineering, the Facilities Technician will be responsible for PMI’s maintenance and equipment support activities. The Facilities Technician performs with minimal supervision preventive maintenance, demand maintenance and calibration tasks on critical equipment, utilities, and facilities. | 8/4/2019 |
| 14477 | PMI Biopharma Solutions Nashville, TN Microbiologist I, Analytical Development BS in biology or related Exp: 0-1 years |
Reporting to the Microbiology Supervisor, the Microbiologist I will be responsible for performing environmental monitoring sampling of ISO class environments and assisting with preparation, characterization, and identification of environmental isolates. He/she will perform raw material and drug product method development and cGMP testing. | 8/4/2019 |
| 14478 | PMI Biopharma Solutions Nashville, TN Chemist I, Analytical Development BS in chemistry/biology or related Exp: 1-2 years in pharma |
The Chemist I position, reporting to the Director, Analytical Development, will operate under moderate supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development. | 8/4/2019 |
| 14479 | PPD South San Francisco, CA Assistant Scientist / Associate Scientist - Small Molecule , Lab Technician BS in biology/chemistry Exp: 0-2 years |
As an Assistant Scientist/Associate Scientist, you will provide analytical support for cleaning verification activities and the testing of non-active materials in support of early phase Small Molecule GMP manufacture of Drug Substance and Drug Product while working onsite at a major client site. You will perform sample analysis, as well as, basic laboratory duties such as accurate weighings, solution preparations, and analytical instrument setup. This is an analytical lab technician position and does not include any operational manufacturing duties. | 8/4/2019 |
| 14480 | PPD Richmond, VA Associate Group Leader - Automation HS Diploma Exp: 0-5 years, 1+ years leadership |
Provides line-level management coordination of resources and work schedules for laboratory activities. Oversees daily operations and assists in preparation and implementation of company policies, quality systems and training programs. Ensures that projects are completed in a timely manner so that company revenues are met and clients are satisfied with the quality and turnaround time of work being performed. | 8/4/2019 |
| 14481 | PPD Middleton, WI Assist Scientist BS/BA Exp: 0-2 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. | 8/4/2019 |
| 14482 | PPD Middleton, WI QA Auditor I - Labs BS/BA in chemistry or related Exp: 1-2 years |
The basic purpose of the Quality Assurance (QA) Auditor is to assure the quality of laboratory data and reports. This is accomplished by reviewing data and reports as specified by SOP's (Standard Operating Procedures), and by conducting project specific audits of laboratory procedures and by writing audit reports. | 8/4/2019 |
| 14483 | Prahs Boston, MA Clinical Trials Associate - Boston BS/BA in clinical, or health sciences Exp: 0-2 years |
As a clinical trial associate, you will assist the Clinical Project Managers in the conduct of trials and may be responsible for managing start up activities, vendor communication, or other project activities as assigned. | 8/4/2019 |
| 14484 | Precision BioSciencesq Durham, NC Associate Process Engineer MS in chemical engineering/biological engineering Exp: 0-2 years |
The Associate Process Engineer works within the Cell Therapy Development team and will participate in process development efforts, delivering best-in-class manufacturing methods for allogeneic T cell therapies. The position will assist in the clinical progression of candidate CAR and TCR T cell therapies by designing and executing process development experiments across a variety of process scales. The Associate Process Engineer will collaborate internally across functional areas as well as externally with industry partners to ensure project advancement, rapid and best-in-class execution, and effective communication of challenges and opportunities. | 8/4/2019 |
| 14485 | Precision Xtract Vancouver, BC Research Statistician - HEOR MS Exp: 1-3 years |
As an Associate Research Statistician you will develop and implement advanced research across a broad portfolio of evidence synthesis and decision modeling research projects. Associate Research Statisticians collaborate with project teams to execute analytical work, as well as contribute to the development of the department as a whole. | 8/4/2019 |
| 14486 | Precision Xtract Frederick, MD Proposal Associate BS in biology, business Exp: 0-2 years |
The Proposal Associate works closely with a cross-functional team to provide responses to laboratory services RFPs and RFIs from government and commercial clients. You will support the proposal process from receipt of RFP through submission and pipeline tracking. Typical duties include attending proposal development meetings, tracking proposal statuses, assisting with developing pricing and text for proposals and quotes, crafting and distributing reports, and tracking opportunities in Salesforce.com. | 8/4/2019 |
| 14487 | Precision Xtract Frederick, MD Facilities & Equipment Technician - Entry/Intermediate Level HS Diploma/GED Exp: 1-3 years |
You will be responsible for preventive maintenance and the repair of refrigeration equipment and monitoring systems for this repository laboratory. You will follow the company equipment/system validation and maintenance program as well as complete simple to intermediate repairs for all equipment related to the repository operations. | 8/4/2019 |
| 14488 | Precision Xtract Frederick, MD Biostatistician I, II or Senior – Clinical Trial Services MS in biostatistics/statistics Exp: Entry Level |
Authoring and reviewing statistical analysis plans, including development of table and listing shells. Providing input into development of case report forms (CRFs). Generating randomization schedules and providing sample size calculations. Generating analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. | 8/4/2019 |
| 14489 | Perrigo Bronx, NY Chemist I BS/BA in chemistry or related Exp: 1 or more years in QC Lab |
To ensure the Quality and Compliance of raw materials, finished products, and stability samples by performing laboratory analytical testing relative to the support of Perrigo operations and manufacturing needs. Responsible for preparing solutions and reagents for testing as required. Uses analytical laboratory equipment such as HPLC, UPLC, GC, UV and IR. Works independently and within team under direction of supervisor to accomplish tasks. | 8/4/2019 |
| 14490 | Perrigo Georgia, VT Process Operator HS Diploma/GED Exp: 3 months + |
Perrigo Nutritionals, in Georgia, VT is looking to add Process Operators to their team. The shift for this position is 6:00 pm–6:06 am requiring shift, weekend, and holiday work (when applicable). Operating and understanding of all processing equipment (HTST/UHT, Homogenizer, clarifier, etc.) and Wet Process Control Systems (WPCS). Operating and understanding of all liquefying equipment (dry and wet) and process controls. Performs general housekeeping and cleans processing equipment and areas. | 8/4/2019 |
| 14491 | Perrigo Allegan, MI QC Chemist BS in sciences Exp: 1-2 years in GMP/FDA regulated environment |
As a QC Chemist, you will perform analytical testing on samples relative to the release of Perrigo materials and product according to cGMP requirements. Collect samples including raw material, finished product, process equipment and environmental. Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations. | 8/4/2019 |
| 14492 | Perrigo Holland , MI 1st Shift Production Supervisor BS/BA in business/management/engineering Exp: 0-4 years |
This position will share specialized knowledge with management in the development and implementation of on-going processes or special projects, and recommend process changes to eliminate repetitive problems. Participate in capacity or budget planning, gather and evaluate information, and make/present recommendations. May test or evaluate materials or process changes and recommend their implementation or rejection, supervise on-going or special maintenance or installation projects, and work with engineering staff to select or evaluate new equipment both on capital projects and ancillary equipment. | 8/4/2019 |
| 14493 | Paragon Bioservices Haramans, MD Quality Control Analyst - Cell Culture AS in life sciences Exp: 1-4 years in GMP clean rooms |
This role is responsible for Quality Control Cell Culture testing to support Phase III/Commercial GMP manufacturing operations and Drug Substance/Drug Product release. Works in a fast-paced environment supporting the quality control department of a CMO for manufacturing of biologic bulk drug substance and sterile finished drug product. Perform adherent and cell culture testing in a Phase III/Commercial GMP Manufacturing facility. Includes but is not limited to: thawing, enumeration, passaging and cryopreservation of various cell line types required for QC assays. | 8/3/2019 |
| 14494 | Paragon Bioservices Haramans, MD Validation Engineer BS or MS in life sciences/engineering Exp: 1-3 years in validation |
The Validation Engineer is responsible for qualifying cGMP manufacturing equipment cleaning, process validation, and aseptic/sterile processes. Generates qualification protocol(s), for various processes in the facility. Oversees the timely completion of all validation documentation, including coordination of contractor activities. Works closely with Manufacturing, QA/QC and Facilities staff in the execution of validation activities, as applicable. | 8/3/2019 |
| 14495 | Paragon Bioservices Baltimore, MD Quality Control Sample Coordinator HS Diploma Exp: 1-2 years in cGMP environment |
Sampling of raw materials according to established specifications. Sample coordination and receipt from other departments for internal and external testing. Scheduling of QC testing and activities. Sending out of test samples to Contract Testing Laboratories (CTL). Works closely with Manufacturing, Analytical Development and Process Development for scheduling of samples submission to the QC lab. May also interact with Project Managers on sample coordination | 8/3/2019 |
| 14496 | Paragon Bioservices Haramans, MD Associate Scientist/Eng. I/II - Downstream Process Development BS or MS in life sciences/chemical engineering Exp: 0-3 years |
The Associate Scientist/Engineer I/II is actively engaged in process and product development within a dynamic team and displays strong technical knowledge, initiative, and scientific commitment, and makes significant scientific and technical contributions to downstream process development. Integral team member in moving projects forward toward GMP Manufacturing for clinical trials, registration, improvements of existing processes and products | 8/3/2019 |
| 14497 | Paragon Genomics Hayward, CA Research Associate BS/BA in biological sciences Exp: 1+ years in NGS lab |
This is a laboratory-based position with great career potential for a junior scientist or prospective scientist who already have or wishes to gain hands-on molecular biology experience in the next-generation sequencing space. Manage orders and logistics of key account(s) to ensure smooth sales to MFG transition. Support Technical Support activities such as troubleshooting and verification studies | 8/3/2019 |
| 14498 | Paramit Morgan Hill , CA Process Engineer BS in Industrial, Mechanical, Electrical, General Engineering or Equivalent technical/engineering experience Exp: 0-1 years |
Establish and evaluate all PCBA manufacturing processes, including Surface Mount Technology and Wave Soldering. Established understanding of printed circuit assembly processes including: solder paste printing, placement, reflow profiling of thermal characteristics, automated inspection parameters, IPC 610 F acceptability requirements. | 8/3/2019 |
| 14499 | Particle Sciences Bethlehem, PA Lab Technician HS DIploma Exp: 0-2 years |
Particle Sciences, Inc. in Bethlehem, PA has an immediate opening for a Formulation Technician. Duties include: Providing assistance and support to formulation scientists. Upkeep, organization and cleaning of common laboratory areas, glassware and equipment parts. Maintenance of lab inventory | 8/3/2019 |
| 14500 | PBL Assay Sciences Piscataway, NJ R&D Scientist I/II/III MS Exp: 0-2 years |
The R&D Scientist is responsible for the hands-on development of immunoassays, such as ELISAs and cell-based assays, for commercial production. This individual plans and executes design, development, and Manufacturing transfer of bioanalytical assays for product commercialization. The R&D Scientist is also responsible for development of custom assays and reagents for clients. | 8/3/2019 |
| 14501 | PBL Assay Sciences Piscataway, NJ Assay Services Scientist I/II BS in life sciences Exp: 1+ years lab experience |
The Assay Services Scientist I / II works primarily with cell culture-based bioassays, executing antiviral bioassays, ELISAs and other highly sensitive immunoassays for characterizing proteins and reagents; analyzing data and drafting client reports; and developing new and custom assays to support the growth of the Assay Services Group. Execute immunoassays on ELISA, and other highly sensitive platforms like Electrochemiluminescence (MSD), Single Molecule Array (Simoa), and Single Molecule Counting (Erenna) | 8/3/2019 |
| 14502 | PBL Assay Sciences Piscataway, NJ Quality Control Scientist I BS/BA in biological sciences Exp: 1-2 years lab experience |
To ensure the quality of PBL reagents the Quality Control (QC) Scientist I will perform release and stability testing of interferons, antibodies, and manufactured ELISA kits. In addition, the QC Scientist I will perform bioassays or immunoassays to troubleshoot relevant customer issues and design and initiate experiments and projects to improve the quality of PBL products. The QC Scientist I may also serve as back up to the Product Development, Assay Services, or Manufacturing departments as needed: such additional duties may include designing and performing ELISA testing protocols, custom bioassays, and solution preparation. This individual will be involved with document control, SOP writing, and recordkeeping. | 8/3/2019 |
| 14503 | PBL Assay Sciences Piscataway, NJ Marketing Support Associate BS/BA in biological sciences Exp: 1+ year in marketing |
Assist in the coordination and implementation of marketing activities with a focused effort on product marketing and management. Provide support for marketing initiatives to further company goals. Execute tactical implementation of initiatives to develop potential customer base and to generate awareness of existing and new PBL products and services. Collaborate in the development of marketing content to promote product and service offerings (e.g. copy writing, eNewsletters, flyers/brochures, etc. Perform marketing elements of product launches including digital marketing efforts | 8/3/2019 |
| 14504 | PCI Pharma Sciences Rockford, IL Project Engineer BS in related field Exp: 1-5 years |
Design packages, processes, and tooling to package pharmaceutical products in a consistent high quality package which complies with cGMP's and customer requirements. | 8/3/2019 |
| 14505 | PCI Pharma Sciences Philadelphia, PA Process Engineer BS in engineering Exp: 0-2 years |
The main functions of a Process Engineer are focused around two key activities of the production area: identifying and mitigating packaging issues for existing business through strong engineering and process improvement methods, and designing and supporting packaging processes for new business. | 8/3/2019 |
| 14506 | PCI Pharma Sciences San Diego , CA IT/ERP Assistant - temporary BS in related field Exp: 1-5 years |
Support implementation of ERP system by perfoming data scrubbing and conversion efforts. Extract, map, and transform data to meet ERP migration requirements. | 8/3/2019 |
| 14507 | PCI Pharma Sciences Rockford, IL Calibration Technician AS/AA in related field Exp: 1-3 years related |
Performs calibration testing on laboratory and plant equipment to assure proper working condition is maintained. Set-up, calibrate, and trouble shoot devices such as temperature, pressure, flow, and humidity instrumentation. Maintain all documentation in an organized and controlled manner in compliance with GAMP and FDA. Trend and analyze performance data to evaluate the effectiveness of calibration systems. | 8/3/2019 |
| 14508 | PCI Pharma Sciences San Diego , CA Business Development Associate BS/BA in related field Exp: 1-5 years |
Working with Business Development Executives, provides high quality clinical packaging and distribution proposals within expected timeframe. Based on quote requirements, works with various internal departments to calculate complex costing in order to deliver Proposals and Change Orders to customer's right first time. Prepares and presents proposals to Business Development Executives and customers during customer facing meetings when applicable. | 8/3/2019 |
| 14509 | PCI Synthesis Devens, MA Process Chemist R&D BS or MS in chemistry Exp: 0-5 years |
The successful candidate is expected to be able to participate in a chemical synthesis program with the objective to develop a chemical process that can be safely performed on large scale. This involves being able to design, adapt and execute synthetic procedures and purification methods on a laboratory scale to fit the requirements of the development or scale-up plant. | 8/3/2019 |
| 14510 | Penumbra Alameda, CA Quality Control Inspector HS Diploma/GED Exp: 1 year of QC |
As a Quality Control Inspector, you will test and inspect components and products in the laboratory. Perform routine inspection at incoming Quality Control and finished device level. Inspect components, products, labels, boxes, pouches, and coatings visually and mechanically. Take measurements using micrometers, calipers, snap gages, gage pins and other measuring instruments. | 8/3/2019 |
| 14511 | Penumbra Alameda, CA QA Engineering Specialist BS/BA in sciences/engineering Exp: 1 or more years in quality systems |
As a Quality Assurance Engineering Specialist at Penumbra, you will support quality engineering activities designed to ensure that all processes, products and systems meet the highest standards of quality and compliance with domestic and international regulations. Verify and document accuracy of sterilization process, biological test results, and completion of Device History Records. Assemble sterile loads and complete associated documents for sterilization. Perform ongoing data entry, review, and analysis of data to support statistical process control. | 8/3/2019 |
| 14512 | Penumbra Alameda, CA Inventory Control Coordinator HS Diploma/GED Exp: 1 year in shipping/receiving |
Maintain the accuracy and control of material receipts, raw material and finished goods inventory locations. Maintain accurate logs and files for receipts, lot control, and daily shipments. Process domestic and international shipments consisting of pulling the order, entering data into the computer system and scheduling carrier pick up. Update and maintain cycle counting on a routine basis with other staff members. | 8/3/2019 |
| 14513 | Penumbra Alameda, CA Engineer I BS or MS in engineering/sciences Exp: 0-2 years, experience preferred |
As an Engineer I at Penumbra, you will work with engineers in the Manufacturing, Research and Development, or Quality groups to support the development and testing of new products; the development and improvement of manufacturing processes; and compliance with Penumbra’s Quality System and all applicable regulations and standards. | 8/3/2019 |
| 14514 | Starkey Eden Prairie, MN Territory Sales Representatives BS/BA Exp: 1+ years |
We are seeking to add a Territory Sales Representative that will be responsible for the growth of gross sales, revenue and average selling price of the assigned territory through creating long-term customer relationships and satisfaction. They will passionately engage with all customers to cultivate relationships and grow market share by providing world-class customer support and education of Starkey products and services. They are responsible for upholding the values and culture of the department through positivity and teamwork. All reps will be expected to adhere to company policies and procedures to accomplish Starkey’s mission of serving our customers better than anyone else. etc. | 7/30/2019 |
| 14515 | Starkey Eden Prairie, MN Mobile Apps Software Engineer - iOS BS/MS computer science/engineering or related Exp: 1+ years |
You will be doing: Building native mobile apps leveraging cross platform technologies. Utilizing Swift, Kotlin, C#/.NET & Cloud platforms. Iterating on design and functionality with our Product Managers and designers. Working closely with a team of mobile developers, testers, product managers. Able to jointly and independently make decisions, define required changes, and communicate modifications to the entire project team. | 7/30/2019 |
| 14516 | Structure Medical Naples, FL Swiss CNC Machinist I HS diploma or equivalent Exp: 1+ years |
Performs entry level specialized computer numerical control (CNC) machinist work for Structure Medical, LLC. Operates CNC machines to run production per approved schedule provided. Work is performed under close supervision with minimal latitude for the use of initiative and independent judgment. Responsible for setting up and operating CNC machines; performs preventative maintenance on machines. Notifies the CNC Programmer of problems with equipment and/or tooling that may cause defects or lost time. Recommends process improvements to resolve problems. etc. | 7/30/2019 |
| 14517 | Stryker Kansas City, MO Associate Sales Rep - Interventional Spine BS/BA Exp: 1-2 years |
As an Interventional Spine Associate Sales Representative, you assist in strategically promoting and selling Stryker IVS products to meet our customers’ needs. You confidently conduct product evaluations in Operating Room and office settings, persuasively demonstrating the value of our products. Systematically tracking your territory progress, you proactively communicate your findings with your Regional Manager and Sales Representative(s) you are supporting to push yourself to exceed each goal. When onsite with clients, you use your product knowledge and quick thinking to solve product problems and inform doctors, nurses and other staff as to the proper use and maintenance of our products. You take great pride in meticulously managing and maintaining your sample inventory of products and are prepared to assist a customer whenever the need arises. etc. | 7/30/2019 |
| 14518 | Sun Pharma Billerica, MA QC Microbiologist I BS in biology or microbiology Exp: 1+ years |
Responsibilities include: Record GMP data, monitors and evaluates QC systems and equipment. Recommend improvements to procedures, and revise SOP’s and GMP documentation as required. Interact with internal and external auditors including government agencies and contract manufacturing representatives. Perform release, stability, validation and complaint follow-up assays on raw materials, in-process and final products. Perform microbial identification related to product and environmental testing. Perform sampling of raw materials as required for QC testing. | 7/30/2019 |
| 14519 | Sword Diagnostics Chicago, IL Research Associate I, Product Applications BS in biology, microbiology, or related Exp: 1-3 years laboratory experience |
Your main responsibilities will be to perform functions in support of Product Application Scientist(s) and other individuals as needed, perform common laboratory testing (including ELISA) using established protocols, prepare buffers and other chemical solutions as needed and use proper personal protective equipment (PPE) and good aseptic technique to handle biological (including human) samples. On a day-to-day basis, you will be expected tosuggest, plan and carry out studies with guidance of supervisor, record data for evaluation, analyze results with guidance of supervisor and assist other lab personnel as needed, maintain organized records of studies performed, and other duties and responsibilities as assigned. | 7/30/2019 |
| 14520 | Syneos Health Richmond, VA Oncology Sales Representative BA/BS Exp: 1-2 years |
This opportunity is with our Selling Solutions Commercial Division, which partners with top tier pharmaceutical, medical device and biotechnology companies to develop and execute sales and marketing strategies that deliver. The selected professional will be an integral part of a nationwide sales team developing and managing an assigned territory. You will: Maximize new business opportunities with physicians and other health service providers. Present therapeutic products and creatively teach people about their usage. Engage in meaningful dialogue that addresses the needs of the health provider and patient. Build trust and credibility and become a true collaborator in commercial success. | 7/30/2019 |
| 14521 | Syneos Health Burlington, MA Statistical Analyst MS in statistics, biostatistics, public health, economics, or related Exp: 0-5 years |
The Statistical Analyst will work with a small team led by the Director, Analytics, Programs and Insights. This Analysis Group provides vital support to all other key functions of the company: research and development, marketing, finance, and operations. Team members analyze patient compliance programs, form hypotheses, dissect patient data, evaluate program performance, and explore trends. The Analyst will be responsible for generating and analyzing reports for management and pharmaceutical clients. Specific responsibilities include running analytical reports in SAS and Excel, assisting in the development of methodology, and collaborating with analytics directors. | 7/30/2019 |
| 14522 | Syneos Health Baltimore, MD Oncology Sales Representative BA/BS Exp: 1-2 years |
This opportunity is with our Selling Solutions Commercial Division, which partners with top tier pharmaceutical, medical device and biotechnology companies to develop and execute sales and marketing strategies that deliver. The selected professional will be an integral part of a nationwide sales team developing and managing an assigned territory. You will: Maximize new business opportunities with physicians and other health service providers. Present therapeutic products and creatively teach people about their usage. Engage in meaningful dialogue that addresses the needs of the health provider and patient. Build trust and credibility and become a true collaborator in commercial success. | 7/30/2019 |
| 14523 | Syneos Health Tampa, FL Oncology Sales Representative BA/BS Exp: 1-2 years |
This opportunity is with our Selling Solutions Commercial Division, which partners with top tier pharmaceutical, medical device and biotechnology companies to develop and execute sales and marketing strategies that deliver. The selected professional will be an integral part of a nationwide sales team developing and managing an assigned territory. You will: Maximize new business opportunities with physicians and other health service providers. Present therapeutic products and creatively teach people about their usage. Engage in meaningful dialogue that addresses the needs of the health provider and patient. Build trust and credibility and become a true collaborator in commercial success. | 7/30/2019 |
| 14524 | Syneos Health Jersey City, NJ Sales Representative BA/BS Exp: 1+ years |
Maximize new business opportunities with physicians and other health service providers. Present therapeutic products and creatively teach people about their usage. Engage in meaningful dialogue that addresses the needs of the health provider and patient. Build trust and credibility and become a true collaborator in commercial success. etc. | 7/30/2019 |
| 14525 | Syneos Health unspecified, PA Quality Analyst I BS/MS in biological or chemical science Exp: 0-1 years |
The QC Analyst/Microbiologist I has the responsibility to: Perform aseptic sampling Pilot Plant critical utilities and controlled environment. Perform general laboratory maintenance activities such as cleaning, inventory, and ordering of laboratory supplies. Perform sample management such as logging samples into LIMS and performing sample reconciliation. Perform basic laboratory assays such as viable and non-viable environmental monitoring, pH, and conductivity in compliance with all applicable procedures and regulations. May perform basic microbial identification testing (eg. Gram stain) with the assistance of more experienced level microbiologist. Assists with the collection of samples for qualification of critical utilities and operations environment in support of the Pilot Plant. etc. | 7/30/2019 |
| 14526 | Syneos Health unspecified, NJ Lab Tech (Bulk Production) AS/BS Exp: 0-2 years laboratory experience |
A Lab Tech Ops is needed for a 6-month contract position a major biotech company in Northeast. Duties: Perform bulk production and production support duties for Operations. Performs a variety of duties relating to production operations. Follows departmental work instructions, SOP's, OSHA safety regulations and cGMPs to perform assigned tasks. Monitor and oversee lab supply inventory, generate expense purchase requisitions, if applicable, input production data and other work-output data into appropriate network (e.g. SAP / LIMS) and maintain documentation in accordance with established procedures. etc. | 7/30/2019 |
| 14527 | Synexus Anderson, SC Research Assistant BS Exp: 1+ years |
Assists the Clinical Research Coordinators in their responsibilities by doing the following: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Assists the Clinical Research Coordinators with updating and maintaining logs and filing in charts; Schedules subjects for study visits and conducts appointment reminders; etc. | 7/30/2019 |
| 14528 | Synthego Redwood City, CA Laboratory Associate, CRISPRevolution AA in chemistry or related Exp: 1-3 years |
We are searching for motivated, enthusiastic, and hands-on individuals interested in advancing science through the manufacturing of our CRISPR products. As a Lab Associate at Synthego, you will join our growing operations team and have direct responsibility for the synthesis and purification of our gRNA products. This role requires a strong attention to detail, a desire to learn and adapt to new processes, and familiarity with safe laboratory practices. This role will combine hands-on laboratory protocols with advanced automation to ensure the timely delivery of high quality products to our customers. etc. | 7/30/2019 |
| 14529 | Synthego Redwood City, CA Shipping Associate, CRISPRevolution unspecified Exp: 1+ years |
Synthego is looking for a shipping associate to execute our daily order fulfillment activities, ensuring quality and customer satisfaction are top priorities. We’re looking for a detail-oriented and highly motivated person who is comfortable working in a fast-paced, dynamic environment. etc. | 7/30/2019 |
| 14530 | Synthego Redwood City, CA Research Associate - Pre Clinical BS in biological sciences Exp: 1+ years in biological lab |
Research Assistant - Pre-clinical will be trained to provide technical support to the senior scientist on a defined project from conception to proof-of-concept in vitro and in vivo. What You'll Do: Process leukopacks and bone marrow to isolate primary cell culture (ie - stem cells and T cells) depending on the project. Maintain and expand primary cells. Test conditions to optimize gene editing of specific cell type. Vector cloning and various molecular biology assays as needed. Viral production. Assist in tissue processing and analyses. etc. | 7/30/2019 |
| 14531 | System1 Biosciences San Francisco, CA Research Associate BS/MS in biological sciences Exp: 1+ years tissue culture experience |
We are seeking a highly motivated junior scientist to join our high-throughput biology operations team. You’ll work with a team of scientists and engineers on these responsibilities and more: Culturing iPSCs. Differentiating iPSCs into neurons. Imaging cells using fluorescent imaging systems. Manipulating cells via transfections, dyes, or viruses. Troubleshooting experiments. Maintain a safe and orderly working environment. etc. | 7/30/2019 |
| 14532 | Takeda Lexington, MA Clinical Research Associate BS/BA Exp: 1+ years |
The in-house Clinical Research Associate (CRA) is responsible for providing support for day to day clinical study activities under general supervision of the the Clinical Project Manager(s). The CRA also provides support for existing departmental tasks and may take on developmental tasks as appropriate upon discussions with manager. The CRA performs work within established protocols under general supervision. etc. | 7/30/2019 |
| 14533 | Takeda San Diego, CA Research Associate Antibody Discovery MS in molecular biology, biochemistry, or related life science Exp: Not necessary for MS candidate |
The research associate will join a fast-paced Biotherapeutic Engineering team within Global Biologics Research. The candidate will perform complex research assignments and will be responsible for the discovery and engineering of therapeutic biologics including antibodies, fusions and other platforms. The candidate will communicate results within the Biotherapeutic Engineering team and with cross functional project team members. ACCOUNTABILITIES: Under minimal supervision, execute discovery and lead optimization projects using display platform technologies with high quality and efficiency. etc. | 7/30/2019 |
| 14534 | Takeda Thousand Oaks, CA Manufacturing Associate I HS diploma/BS Exp: 0-2 years |
The Manufacturing Associate I is responsible for executing all manufacturing department processes while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate I is expected to fully participate in both departmental projects and any quality working teams that may be applicable. This position shall be responsible for the hands on execution of activities as they relate to the manufacturing of products. Essential Duties and Responsibilities: Formulation/Filling: Participate in bulk formulation, aseptic filling, Lyophilization, and capping operations. Executes processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. etc. | 7/30/2019 |
| 14535 | Takeda Thousand Oaks, CA Manufacturing Associate I HS diploma/BS Exp: 0-2 years |
The Manufacturing Associate I is responsible for executing all manufacturing department processes while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate I is expected to fully participate in both departmental projects and any quality working teams that may be applicable. This position shall be responsible for the hands on execution of activities as they relate to the manufacturing of products. Responsibilities: Cell Culture/Purification: Support Cell Culture/Purification operations for the production of a bulk drug substance product. Prepare media and buffer solution. Clean, Set up, operate, and teardown of equipment such as tanks, filtration systems, carton assembler, bioreactors, and production lines. etc. | 7/30/2019 |
| 14536 | Takeda Round Lake, IL Production Associate AS/AA Exp: 0-2 years |
The Production Associate (PA) is responsible for executing all processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, responsible for the hands-on execution of all activities in the production area. | 7/30/2019 |
| 14537 | Takeda Social Circle, GA Manufacturing Associate I AA or equivalent Exp: 1 year |
This position is expected to : clean, set up, operate, and teardown equipment such as tanks, filtration systems, chromatography columns/skids, and production lines (fill lines, inspection lines, packaging lines). In addition, the technician will operate general production equipment such as pH, UV, and conductivity meters, washers, and additional equipment associated with the production process. Monitoring and recording of critical process parameters is required. Perform basic preventive maintenance related to manufacturing equipment. Support the implementation of Kanban and 5S systems to assist the full production environment. Must be able to read and follow detailed written/electronic instructions, be comfortable with electronic documentation, and have good verbal/written communication skills. | 7/30/2019 |
| 14538 | Talis Biomedical Menlo Park, CA Research Associate MS in biology, microbiology, biochemistry, or related Exp: 0-3 years |
The candidate will join the Assay Development group in the R&D division where focus is on molecular assays development such as nucleic acid isolation, purification, amplification and labeling technologies. We are seeking talented, motivated individuals to join a collaborative effort to enable development of rapid diagnostic tests of several pathogens from various clinical specimens. Position Responsibilities: Work with senior scientists and run hands-on experiments for microbiology, sample preparation, nucleic acid extraction and amplification. Participate in design of molecular assays. etc. | 7/30/2019 |
| 14539 | Talis Biomedical Menlo Park, CA Accounting Associate BS/BA in accounting Exp: 0-3 years |
The Accounting Associate will be responsible for day to day accounting tasks and will have ownership over the accounts payable process. This role will support the Senior Accountant in maintaining the general ledger. Ideal candidates will have a Bachelor’s degree or equivalent in Accounting and the ability and desire to work in a fast paced and dynamic environment. The successful candidate will report directly to the Sr. Director, Finance and play an instrumental role in the financial growth of the Company. etc. | 7/30/2019 |
| 14540 | Tanvex BioPharma San Diego, CA Research Associate, Purification - #1203 BS in chemical/biochemical engineering, biochemistry, or related Exp: 0-3 years protein purification |
The Research Associate performs basic trouble-shooting of processes, instrumentation, and equipment with guidance, contributes to technology transfer from process development to clinical cGMP manufacturing (including definition of bill of materials and batch record drafting/review), and performs bench scale experiments such as sterile membrane filtration, depth filtration, tangential flow filtration, viral clearance filtration, as well as chromatography. The Research Associate will collaborate with cell culture, formulation, analytical and manufacturing for achievement of project tasks and authors internal reports at appropriate milestones with supervisory guidance. | 7/30/2019 |
| 14541 | Tanvex BioPharma San Diego, CA Research Associate, Formulation - #1202 BS in chemical/biochemical engineering, biochemistry, or related Exp: 0-3 years formulation development |
The Research Associate in our Formulation group is responsible for executing experiments related to formulation development from formulation definition, to stability program design and execution to support pipeline projects. This position will effectively apply basic scientific principles in formulation screening, biochemical characterization, drug substance and drug product configuration, delivery compatibility, and technology transfer activities associated with the development of biopharmaceutical formulations. The Research Associate will execute relatively simple scientific experiments which contribute to project milestones; performs analytical test methods including but not limited to spectrophotometry, pH, liquid chromatography and capillary electrophoresis; and performs basic trouble-shooting of assays, instrumentation, and equipment with guidance. etc. | 7/30/2019 |
| 14542 | Tanvex BioPharma San Diego, CA Research Associate, Analytical Sciences - #1189 BS/MS in chemistry, biochemistry, chemical/biochemical engineering or related Exp: 0-3 years |
The Research Associate will perform analytical tests using HPLC, Spectrophotometry (RP, IEX, SEC, HILIC etc.), CE, mass with high quality and efficiency; provides analytical support in R&D settings for samples from various process scales; writes experiment summaries and development reports; and assists during document review comprising of but not limited to: batch records, standard operating procedures and assay protocols. etc. | 7/30/2019 |
| 14543 | Tanvex BioPharma San Diego, CA QC Associate, BioAssay - #1167 BS in molecular biology, chemistry, biochemistry, or related Exp: 0-2 years |
The QC Associate is responsible for routine and non-routine product testing using biochemical methods such. Additional responsibilities include assisting with transferring analytical methods from development into the QC laboratory and test method validation; generating test results and reporting results for the assigned GMP testing in a timely and compliant manner; sample coordination, lab equipment maintenance, QC document management and review. Knowledge of performing cell-based assay, immuno-assays, and/or QPCR assays in a GMP environment is essential. etc. | 7/30/2019 |
| 14544 | Stryker Portage, MI Assembler I unspecified Exp: No experience |
Assembles mechanical units, fabricated parts/components and/or electrical/electronic systems to make subassemblies, assemblies or complete units using hand tools, power tools, jigs, fixtures and miscellaneous equipment. Fits, aligns, calibrates and adjusts parts and mechanisms to meet tolerances and product operating requirements; repairing units or products that have failed to meet requirements. | 7/30/2019 |
| 14545 | Stryker Portage, MI Associate Customer Experience Representative (10:30am - 7:00pm) HS diploma or equivalent Exp: 1 year |
Responsibilities: Answers incoming requests through a multichannel system which include but are not limited to order entry, order status and trouble shooting of products. Follow standardized process to ensure 100% quality for all orders. Accountable for all record-keeping as appropriate and in accordance with Stryker specifications. Understands, interprets and explains detailed information of printed material and processes. Prioritizes and identifies activities and tasks, adjusting priorities when appropriate. Abides by company, departmental policies and regulatory procedures. etc. | 7/30/2019 |
| 14546 | Stryker Portage, MI Associate Customer Service Representative BS/BA Exp: 1-2 years |
Provides customer services relating to sales, sales promotions, installations and communications. Ensures that good customer relations are maintained and customer claims and complaints are resolved fairly, effectively and in accordance with the consumer laws. Develops organization-wide initiatives to proactively inform and educate customers. Develops improvement plans in response to customer surveys. etc. | 7/30/2019 |
| 14547 | Stryker Longview, TX Associate OnSite Repair Specialist Associate degree Exp: 1-2 years |
The following is not intended to represent an all-inclusive list of job responsibilities, but to outline the ESSENTIAL FUNCTIONS of the position.General Description:Training period to become proficient in providing maintenance and repair services on surgical instruments and equipment.The Surgical Instrument Repair Excellence (SIRE) Apprenticeship Program is a two to three-year process that is monitored by the Department of Labor (DOL). The first 4 6 months of initial training will be based out of the Houston Training Center (HTC). After completion of the training at HTC you will be required to spend the remainder of the introductory 6 months with established field personnel at their home sites.Essential Functions: * Learn and become proficient in all aspects of handheld stainless steel instrument sharpening, repair and maintenance (Maintain an average score of 80% on all written and technical assessments). etc. | 7/30/2019 |
| 14548 | Stryker Portage, MI Marketing Communications Associate BS/BA in business, marketing, or related Exp: 0-2 years |
The Marketing Associate is responsible for sales support initiatives, including the development of new marketing materials, maintenance of existing materials and the overall enhancement of HCS marketing communications. This individual will need to understand and drive the Healthcare Systems brand as well as develop creative marketing templates, ensuring consistency in materials. Provides sales support to Corporate, National and Government Accounts teams by fielding questions, aiding in customer presentation development, gathering specific information from business unit marketing teams and maintaining price files. etc. | 7/30/2019 |
| 14549 | Stryker San Josa, CA Packaging Test Engineer BS in Packaging Engineering/Science Exp: 1-3 years |
Test Engineers work closely with R&D to experiment with early prototypes and vet out product designs throughout the design process. What this really means is that we get to be the Mythbusters of our division. You think your design can last the entire expected service life? We put it to the test. Just like the show, we quickly design and build fixtures to simulate real life situations. In addition to these experiments, we are ultimately responsible for design verification – the quantitative testing of the technical specifications of the product. We are a close-knit team of more than twenty engineers, technicians, and managers. Our experience ranges from 1 to over 15 years with technical specialties ranging from sterilization, mechanical, electrical, software, optics, packaging, and reprocessing. If you’re the type of person that has the magic ability to break things – we want you! etc. | 7/30/2019 |
| 14550 | System Biosciences Palo Alto, CA Customer & Technical Support Representative (CSR/TSR) BS in life sciences Exp: 1-2 years |
SBI seeks to hire a customer and technical support representative. The ideal candidate will have a B.S. degree in the life sciences and will support an existing group of customer support personnel taking telephone orders from customers, logging into a CRM system, printing packing slips, sales orders, and shipping documentation, and assist with packaging of life science reagents for shipment to worldwide customers. This position will also provide support to the Commercial Team. This is a fast-paced position requiring attention to detail, technical knowledge of life sciences (as telephone conversations with customers will require technical understanding of SBI's products and service offerings, and some technical support), and an ability to multi-task with tight deadlines. | 7/30/2019 |
| 14551 | Taconic Biosciences Germantown, NY Temporary Services Technician AS/BS in life sciences or related Exp: 1 year |
We are seeking an Temporary Services Technician to join our team in our Germantown, NY location. This will be a three month temporary assignment. Services Technicians are responsible for animal husbandry – caring for laboratory animals (mice and/or rats) in designated areas. These individuals ensure that high standards of animal welfare are met, and that the animals are fed, clean, and cared for. Services Technicians are also responsible for assisting with the breeding of animals and performing biopsies as necessary, as well as maintain accurate inventory records. etc. | 7/30/2019 |
| 14552 | Taconic Biosciences Germantown, NY Services Technician AS/BS in life sciences or related Exp: 1 year |
We are looking for a Services Technician to join our Germantown location. This position will be part time, with the following schedule: Friday Mornings - 4 hours, Saturday Mornings - 4 hours, and Sundays - 8 hours. Service Technicians are responsible for animal husbandry – caring for laboratory animals (mice and/or rats) in designated areas. These individuals ensure that high standards of animal welfare are met, and that the animals are fed, clean, and cared for. Service Technicians are also responsible for assisting with the breeding of animals and performing biopsies as necessary, as well as maintain accurate inventory records. etc. | 7/30/2019 |
| 14553 | TCR2 Therapeutics Cambridge, MA Clinical Trial Associate BS/BA Exp: 1-2 years |
Responsibilities: Supports the clinical study teams in the execution and delivery of studies. Organizes, manages, and oversees the Trial Master File to maintain up-to-date regulatory documentation for all research sites. Responsible for study laboratory sample management, including tracking and vendor management support. Collect trial information and disseminate it to the internal project team, the CRO, and other stakeholders. etc. | 7/30/2019 |
| 14554 | Smith & Nephew Memphis, TN Distribution Associate I HS diploma or equivalent Exp: 0-1 years |
The Distribution Associate I will interact with the WMS, TMS, RF scanning and/or other warehouse equipment to perform intermediate level distribution tasks in accordance with defined job processes. They will perform these tasks with a focus on safety, quality and productivity. They must comprehend and demonstrate compliance with Standard Operating Procedures and work instructions. The Distribution Associate I is responsible for providing constructive input to enhance the work process and environment. | 7/23/2019 |
| 14555 | Smith & Nephew Memphis, TN Machinist HS diploma or equivalent Exp: 6 months |
This position requires a person to perform simple set ups and operate manual/CNC equipment to manufacture medical components from raw material in a team based environment. Must be able to comply with all governing rules including S.N.E. policies and procedures and adhere to safety and cleanliness practices in the work place. This position works under close supervision. Essential Duties And Responsibilities: Machine medical components, including but not limited to: Perform simple set ups and operate manual/CNC equipment, including turning, milling, grinding, drilling, tapping, EDM and honing. etc. | 7/23/2019 |
| 14556 | Smith & Nephew Philadelphia, PA Associate Account Manager BS/BA Exp: 1+ years in B2B sales |
What you’ll do: You will support Account Manager(s) to address the business needs and goals within the district or region, promoting key brands such as Grafix™ within acute care facilities. You will act as the Account Manager in open territories needing coverage. You will use your organizational skills to coordinate availability of products for hospital outpatient departments. You will use your knowledge and expertise to provide in services to appropriate personnel and to educate end users on the clinical benefits of products. etc. | 7/23/2019 |
| 14557 | Smith & Nephew Phoenix, AZ Associate Account Manager BS/BA Exp: 1+ years in B2B sales |
What you’ll do: You will support Account Manager(s) to address the business needs and goals within the district or region, promoting key brands such as Grafix™ within acute care facilities. You will act as the Account Manager in open territories needing coverage. You will use your organizational skills to coordinate availability of products for hospital outpatient departments. You will use your knowledge and expertise to provide in services to appropriate personnel and to educate end users on the clinical benefits of products. etc. | 7/23/2019 |
| 14558 | Smith & Nephew Memphis, TN Finisher II HS diploma or equivalent Exp: Entry level |
The Finisher II will perform finishing techniques such as buffing, polishing, grinding, deburring and etching on machine products. Achieve proper size, finish and quality following drawings and quality specifications. Performs routine visual inspection and also uses basic measuring equipment. | 7/23/2019 |
| 14559 | Smith & Nephew Memphis, TN Quality Assurance Inspector I HS diploma or equivalent Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. RESPONSIBILITES: Inspect raw materials, components, assembled product, semi-finished product & finished product per inspection procedures/drawings and to print specifications. Utilize attribute and variable measuring equipment/gauges as well as mating parts to determine as found/as left conditions of product. etc. | 7/23/2019 |
| 14560 | Smith & Nephew Pittsburgh, PA Administrative Assistant I Associate degree Exp: 1-3 years |
Provide administrative support to Facility Manager and general office support to Robotics management and staff. Manage all aspects of office administration for smooth operation of facilities and comfortable, productive environment. Respond to all assignments and requests timely and efficiently; maintain discretion on all confidential or sensitive matters. Support corporate safety directives, policies and procedures; proactively contribute to wider HSE and housekeeping improvement goals. Uphold culture of camaraderie and employee engagement while promoting appreciation, trust and respect. | 7/23/2019 |
| 14561 | Smithers Avanza Wareham, MA Entry Level Technical Report Writer BA/BS in environmental science or related Exp: 0-2 years of laboratory experience |
We are seeking a full-time Technical Report Writer to join our talented team. This position will support the needs of the Smithers Viscient organization. The candidate will be responsible for writing and editing high quality study reports for several technology groups, including ecotoxicology, environmental fate and metabolism, avian and analytical chemistry, in addition to production of other documents as needed. Prepares study reports from data presented in technical format that meets guideline requirements. Compiles and incorporates comments from several different levels of review. etc. | 7/23/2019 |
| 14562 | Smithers Avanza Wareham, MA Chemistry Technician II BS in chemistry or related Exp: 6 months laboratory experience |
Position is expected to perform varied and often complex and difficult procedures somewhat independently. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Operates and may maintain, under supervision, test equipment and apparatus of moderate complexity. May provide information for initial data interpretation and test system conformance to expectations. Records, compiles and reduces laboratory data in real time in a complete and thorough manner for individual assignments. May produce reports. etc. | 7/23/2019 |
| 14563 | Smiths Medical Southington, CT Team Technician - 2nd Shift HS diploma or associate degree Exp: 1-2 years |
The Team Technician is responsible for ensuring the correct operation of automatic and semi-automatic assembly production equipment in accordance with governing documentation. This person will also initiate action to prevent the occurrence of nonconformances related to the product and equipment. Additionally, this role will identify and record problems relating to the product, process and or quality system. The Team Technician will also initiate recommendations, provide solutions, and verify the affectivity of continuous operational improvements. etc. | 7/23/2019 |
| 14564 | Smiths Medical Southington, CT Technician I - Medical Device HS diploma or equivalent Exp: 1 year |
The Mechanical Technician I will: Correctly and safely utilize the R&D lab facility and equipment to perform inspection and testing for the evaluation of components and processes to support R&D projects. Performs product/component inspection and testing and organizes maintains laboratory equipment and supplies. Prepares worksheets for data collection, performs data entry and analyzes test data. Assists in the development, documentation and validation of non-standard test methods | 7/23/2019 |
| 14565 | Smiths Medical Dublin, OH Production Group Lead - 2nd Shift HS diploma or equivalent Exp: 1-2 years |
Duties & Responsibilities: Demonstrate leadership and accountability in providing and sustaining a positive safety culture. Provide support for safety training, meetings, and programs. Ensure proper instruction is provided on responsibilities and safe job performance (on the job training). Provide support for safety training, meetings, and programs. Attend passdown meetings, noting key quality and output issues. Observe and communicate out of the ordinary situations and ensure issues are resolved. Collect performance sheets at the end of the shift and give them to the Production Supervisor for entry in the passdown document. Make decisions of priority and value added impacts with regards to safety, quality, customers, and efficiencies. etc. | 7/23/2019 |
| 14566 | Smiths Medical Dublin, OH Quality Coordinator (3rd shift) HS diploma or equivalent Exp: Entry level |
The Quality Coordinator inspects and audits the quality of the product and determines acceptability of product based upon Good Manufacturing Practices (GMP) and inspection procedures. This position is for 3rd shift, Monday-Friday, 10:30pm-7am. Duties & Responsibilities: Determine acceptance, non-conformance, or rework requirements of units working from PCO’s, blueprints, or established operating procedures. Generate documentation files. Monitor procedures to ensure compliance and report discrepancies to Supervisor. Provide feedback on quality findings to appropriate personnel. | 7/23/2019 |
| 14567 | STAAR Surgical Monrovia, CA Quality Engineer Advanced degree in quality engineering Exp: 1 year |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: Support site production, operations, and quality and R&D teams by addressing emergent issues that might arise due to the operation processes. Serve as the quality representative during any product or process investigation. Lead investigations including root cause analysis and health risk assessment of the identified product or process nonconformities. Prepare and execute validations, technical studies, test method validations and other studies / reports as required. This includes preparation of protocols, establishment of test methodology and acceptance criteria, training personnel, execution, data analysis, investigation, and writing final reports. Initiate and lead project teams on non-conformance investigations regarding component failures, finished goods failures, and product returns. This includes but is not limited to performing risk analysis, determining root cause and recommending corrective action. etc. | 7/23/2019 |
| 14568 | STAAR Surgical Monrovia, CA Regulatory Affairs Associate BS in relevant field, advanced degree preferred Exp: 1-5 years |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: Plan, prepare and review all aspects of ongoing and new regulatory submissions, both U.S. (e.g., PMA, IDE, 510(k), PMA Annual Reports, etc.), and international (e.g., CE Technical Files, Design Dossiers, APAC, etc.). Provide regular status updates and activity reports. Review/Prepare Standard Operating Procedures (SOPs). Compile information necessary for periodic reports for Regulatory filings. Preparation and maintenance of annual renewals of Establishment Registrations, State Manufacturing licenses, Device Listing, and other pertinent domestic and international licensing. etc. | 7/23/2019 |
| 14569 | STAAR Surgical Monrovia, CA Regulatory Affairs Specialist BS in relevant field Exp: 1-5 years |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: Plan, prepare and review all aspects of ongoing and new regulatory submissions, both U.S. (e.g., PMA, IDE, 510(k), PMA Annual Reports, etc.), and international (e.g., CE Technical Files, Design Dossiers, APAC, etc.). Provide regular status updates and activity reports. Review/Prepare Standard Operating Procedures (SOPs). Compile information necessary for periodic reports for Regulatory filings. Preparation and maintenance of annual renewals of Establishment Registrations, State Manufacturing licenses, Device Listing, and other pertinent domestic and international licensing. etc. | 7/23/2019 |
| 14570 | Starkey Eden Prairie, MN Corporate Receptionist High school degree or equivalent Exp: 1 year |
All Corporate Receptionists will be responsible for consistently serving our customers by providing the “Human Touch” by answering every call and greeting campus guests in a professional, friendly and efficient manner. As a Corporate Receptionist you are the voice of Starkey answering on average 700 calls per day. Company knowledge is the key to executing this goal and directing the customer accurately and efficiently. Corporate Receptionists will be responsible for upholding the values and culture of the department through positivity and teamwork. As an active team member, they will act as a support system for internal and external customers. All Corporate Receptionists will be expected to serve our customers with passion, purpose and excellence while adhering to company policies and procedures. etc. | 7/23/2019 |
| 14571 | Starkey Eden Prairie, MN Retail Digital Marketing Assoc - Content BS/BA in marketing or related Exp: 0-2 years |
Starkey Hearing Technologies is seeking to add a Retail Digital Marketing Associate - Content. This person is responsible for supporting the Retail Digital Marketing teams with development and maintenance of our customer website programs. This position will collaborate with the Retail Digital Marketing Strategist on the execution and reporting of campaigns across all digital channels. The Retail Digital Marketing Associate will make regular website updates and make recommendations on how to improve website performance, user experience and lead performance. etc. | 7/23/2019 |
| 14572 | Starkey Eden Prairie, MN Administrative Assistant I Some college or degree Exp: 1+ years |
Starkey Hearing Technologies is seeking to add a Commercial Administrative Assistant. The Commercial Administrative Assistant is responsible for supporting the Marketing department along with North American and International Sales. The position is responsible for calendar and phone management, travel and expense assistance, department communications and office supply management. The position will be responsible for coordinating specific department projects for the Commercial organization. This role requires a high standard of internal and external customer service. Follow-through is a must. This role requires a high level of professionalism along with clear and timely communication. etc. | 7/23/2019 |
| 14573 | Starkey Eden Prairie, MN Sales Operations Associate BS/BA or equivalent Exp: 1-2 years |
We are seeking to add a Sales Operations Associate that will execute a wide range of sales operations tasks and projects aimed at improving the efficiency and effectiveness of the sales team. Other duties and tasks come with this role and will be added regularly to support the changing needs of the sales team and sales leadership. etc. | 7/23/2019 |
| 14574 | Starkey Eden Prairie, MN Research Audiologist I Graduate degree in audiology Exp: 1 year |
We are looking for a Research Audiologist that will be responsible for research, subject and data management related to activities pertaining to Alpha and Beta product evaluations, pilot testing, and hearing aid fitting methods. This position will assist in determining the direction of product development. Work will be collaborative with other researchers and personnel in Minnesota. etc. | 7/23/2019 |
| 14575 | Starkey Eden Prairie, MN Digital Marketing Associate (Facebook Ads) BS/BA Exp: 1-2 years with Facebook's ad platform |
Are you interested in Facebook advertising and lead acquisition? Do you want to be a part of a company that seeks to help people improve their lives? We are seeking a Facebook advertising professional/specialist/coordinator to join a strong team focused on paid acquisition efforts, and to ultimately build and grow our marketing initiatives to meet business goals. The ideal candidate has strong interest in Facebook advertising and is willing to roll up their sleeves to get involved with the detailed execution of initiatives. etc. | 7/23/2019 |
| 14576 | Starkey Eden Prairie, MN Facilities Coordinator Associate degree Exp: Not necessary for associate degree |
We are looking to add a Corporate Project Manager that will be responsible for the review, coordination, communication and timely resolution of all Facility related tickets and issues. In a shared-services environment, the scope of this position includes: Retail, Corporate HQ, and global facilities. You will be responsible for resolution performance driving customer satisfaction. etc. | 7/23/2019 |
| 14577 | Statistics and Data Corporation Tempe, AZ Biostatistician MS in biostatistics, statistics, or related Exp: 1-3 years |
Supports lead biostatistician on clinical studies; may serve as lead biostatistician with oversight from a more senior biostatistician. Maintains the statistical integrity of clinical trials analyzed by SDC. Assists in preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, and writing statistical sections of clinical study reports. Primary Responsibilities: Assist in writing statistical analysis plans ensuring appropriate regulatory requirements and study objectives defined in the study protocol are followed. Review CRFs to ensure consistency with protocol and adequacy in collecting data to meet objectives and statistical analyses defined in the protocol. etc. | 7/23/2019 |
| 14578 | Stereotaxis Saint Louis, MO Field Service Engineer - (FSE.6) Associate degree in electronics or equivalent Exp: 1-5 years |
Provide on site and remote service and support of Stereotaxis magnetic navigation systems including permanent magnets, and servo control systems. Interface with customers and vendors to ensure a quality service experience and that all expectations are met. ESSENTIAL JOB RESPONSIBILITIES: Interface with customers to obtain accurate details of the equipment service needs and provide updates regarding the progress of the service/installation. Diagnose and repair control servo control systems. etc. | 7/23/2019 |
| 14579 | Steri-Pharma Syracuse, NY Facilities Maintenance Technician, 2nd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of facilities equipment for effective plant operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to facilities equipment as needed. Provides troubleshooting on complex issues and leads training efforts. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. etc. | 7/23/2019 |
| 14580 | Steri-Pharma Syracuse, NY Production Maintenance Technician, 1st Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. etc. | 7/23/2019 |
| 14581 | Steri-Pharma Syracuse, NY Production Maintenance Technician, 2nd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. etc. | 7/23/2019 |
| 14582 | Steri-Pharma Syracuse, NY New! Warehouse Technician - 1st Shift HS degree Exp: 1+ years |
This position is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. You will: Loads and or unload materials using proper methods and procedures for securing materials. Receives, selects and prepares materials for relocation to end users. Ensures accuracy of shipments and supporting documentation, receiving incoming material and routing to appropriate area or personnel, filling work orders, packaging assemblies and receiving into finished goods, ensuring inventory transaction are accurately logged and overseeing cycle counts and reconciliation activities. etc. | 7/23/2019 |
| 14583 | Steri-Pharma Syracuse, NY Quality, Microbiology Analyst, Crossover Shift, 1st - 2nd BS Exp: 1-3 years in a laboratory setting |
This position performs environmental monitoring and quality control of aseptic process area, to include testing of finished products, raw materials, and components according to established procedures. Position reviews records for accuracy. Position applies standard concepts, practices, and procedures within the laboratory. Position performs a variety of tasks. You will: Performs a variety of micro testing on finished products, raw materials, and components. Performs environmental monitoring in areas of varying aseptic classification. Performs data entry and prepares various reports. etc. | 7/23/2019 |
| 14584 | Steris Syracuse, NY Repair Technician HS diploma or equivalent Exp: 1-3 months |
The primary role of the Repair Technician is to perform repairs on medical instrumentation. Technicians will be trained to become familiar with various types of surgical instruments and understand how to best maintain and repair them. Repairs are completed on a repair truck onsite at a hospital or surgery center. In addition to repair work, Technicians may work with a team including Sales Representatives and RCs (Repair Consultants/Managers) to identify and capitalize on revenue opportunities. Travel requirements may vary by location. etc. | 7/23/2019 |
| 14585 | Steris Birmingham, AL Technician I HS diploma or equivalent Exp: 1-2 years |
The primary role of the Repair Technician is to perform repairs on surgical devices and medical instruments. Technicians will be trained to become familiar with various types of surgical devices and instruments and understand how to best maintain and repair them. Repairs are completed at company repair center. All repairs completed to the highest quality standards and in a timely manner. Duties: Identifies surgical devices and instruments by various types, uses and functionality. Inspects devices and instruments to determine what type of repair and/or adjustment is required. etc. | 7/23/2019 |
| 14586 | Steris Chattanooga, TN Operating Room Liaison - Travel Associate degree or equivalent Exp: 1 year |
Coordination and oversight of daily activities between the OR and Sterile Processing Department (SPD) to facilitate efficient case flow. Responsible for assisting in projects and process improvement initiatives in compliance with contractual obligations. Promotes customer service/satisfaction through training, education, and resolution of OR frictions for the facility. Perform duties in accordance with hospital, TJC, AORN, AAMI and other appropriate policies and procedures. This is a full-time position (non-contract) that provides benefits, paid time off and paid holidays. 75-100% travel. etc. | 7/23/2019 |
| 14587 | Steris Melbourne, FL Repair Technician HS diploma or equivalent Exp: 1-3 months |
The primary role of the Repair Technician is to perform repairs on medical instrumentation. Technicians will be trained to become familiar with various types of surgical instruments and understand how to best maintain and repair them. Repairs are completed on a repair truck onsite at a hospital or surgery center. In addition to repair work, Technicians may work with a team including Sales Representatives and RCs (Repair Consultants/Managers) to identify and capitalize on revenue opportunities. Travel requirements may vary by location. etc. | 7/23/2019 |
| 14588 | Steris Birmingham, AL Operating Room Liaison - Travel Associate degree or equivalent Exp: 1 year |
The Operating Room Liaison individual will work to coordinate and have oversight of daily activities between the Operating Room (OR) and Sterile Processing Department (SPD) to facilitate efficient case flow. Responsible for assisting in projects and process improvement initiatives in compliance with contractual obligations. Promotes customer service/satisfaction through training, education, and resolution of OR frictions for the facility. Perform duties in accordance with hospital, TJC, AORN, AAMI and other appropriate policies and procedures. etc. | 7/23/2019 |
| 14589 | Steris Lincoln, NE Field Service Technician (Floater) Associate degree in electronics, mechanical, or similar Exp: 1 year |
The Field Service Technician provides preventive maintenance, troubleshooting, repair, calibration and installation support on various mechanical, electro-mechanical, and electronic units. The Technician Interacts with customers on a daily basis and completes associated administrative tasks as required. Think of this as an electrical-mechanical-plumber-Customer Service Technician all rolled into one! Every day, something special happens at STERIS. What will YOU help us do next? Duties: Perform preventive and corrective maintenance required on STERIS and related product lines. This includes: disassembling, replacing, or repairing defective parts; reassembling as required; troubleshooting, adjusting/calibrating ready for use by using standard and specialized tools by using technical manuals etc. Troubleshoot, repair or refurbish standard and special purpose equipment and systems components. etc. | 7/23/2019 |
| 14590 | Steris Minneapolis, MN Repair Technician - no experience required HS diploma or equivalent Exp: 1-3 months |
The primary role of the Repair Technician is to perform repairs on medical instrumentation. Technicians will be trained to become familiar with various types of surgical instruments and understand how to best maintain and repair them. Repairs are completed on a repair truck onsite at a hospital or surgery center. In addition to repair work, Technicians may work with a team including Sales Representatives and RCs (Repair Consultants/Managers) to identify and capitalize on revenue opportunities. Travel requirements may vary by location. etc. | 7/23/2019 |
| 14591 | Strata Oncology Ann Arbor, MI Laboratory Assistant AS in a relevant field Exp: 1+ years |
The ideal candidate possesses a basic working knowledge of histopathology and/or molecular biology with entry level experience in basic laboratory techniques and strong data entry skills. The Laboratory Assistant is responsible for receiving and accessioning samples into the Laboratory Information Management System as well as assisting the Histology team with basic tasks and functions required to maintain the smooth operation of the company such as clerical duties, reagent preparation, and inventory. etc. | 7/23/2019 |
| 14592 | Stratos Genomics unspecified, Research Associate—Molecular Engineering MS/BS in chemistry, organic chemistry, chemical engineering, or related Exp: 1-2 years relevant laboratory experience |
We are seeking motivated Scientists and Research Associates to join our team. Candidates will be involved in synthesizing our unique building blocks for our novel DNA sequencing technology, Sequencing by Expansion, developing and optimizing synthesis protocols as well as proposing and executing innovative experiments to push our technology forward. This position requires an availability to work between the hours of 8am to 7pm with extended work hours when necessary. etc. | 7/23/2019 |
| 14593 | Stemina Biomarker Discovery Madison, WI Technical Sales and Marketing Associate Bachelor's degree in marketing, communications, or related Exp: 1-2 years |
Job Purpose: To provide sales and marketing support for both business units of Stemina Biomarker Discovery. Essential Job Duties and Responsibilities: Manage lead generation and tracking using the CRM Salesforce, the marketing automation system Pardot, social media platforms, web traffic tracking systems, and other marketing tools. Manage and build the current database for both business units. Create content using these marketing tools, including regular marketing emails, social media posts, website content, conference materials, print collateral, and other communications as needed for both business units. Manage all social media engagement on LinkedIn, Twitter, and Facebook for both business units, plus Instagram (NeuroPointDX only). etc. | 7/23/2019 |
| 14594 | Bausch Health Lynchburg, VA Distribution Associate I HS Diploma Exp: 6 months + |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Follow prioritized assignments, providing customer service support and ensure the completion of order fulfillment (picking, packing, manifesting), maintain inventory through putaway, breakdowns, replenishment, and cycle count in a timely manner, meeting or exceeding productivity and quality standards. | 7/21/2019 |
| 14595 | Bausch Health Lynchburg, VA Distribution Associate I HS Diploma Exp: 6 months + |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader. | 7/21/2019 |
| 14596 | Bausch Health Clearwater, FL Production Associate II HS Diploma/GED Exp: 1 or more years training lathes/milling machines |
Setup, maintain and operate production line equipment to produce intraocular lenses according to production specifications and standards. Perform inspections to verify accuracy of machining against specifications to maintain quality and performance standards using set up equipment. Conduct initial troubleshooting for defect causes and machine problems . Make minor mechanical repairs as required to maintain production specifications and standards. Report unusual conditions and problems to supervisor and practice good housekeeping. Support, encourage and participate in team related activities; report ideas or suggestions to supervisor. | 7/21/2019 |
| 14597 | Orthofix Lewisville, KY Marketing Associate - Global Spine BS/BA Exp: 1+ years in medical device/pharma marketing |
Working under the direction of senior marketing personnel, the individual will initiate, coordinate and / or execute a wide variety of marketing tasks to help drive adoption and education of the Global Spine product lines. Execute strategic and tactical plans to support market growth of the Global Spine products. Collaborate with the Events Planning team to coordinate and manage Global Spine trade show activities. Develop and maintain Global Spine engagement on social media channels such as LinkedIn, Facebook, Twitter and YouTube, and identify new opportunities where Global Spine should interact in the future. | 7/21/2019 |
| 14598 | Orthofix Lewisville, KY Inspector I - Contractor HS Diploma Exp: 1 year in quality |
Perform receiving inspection on incoming materials, in-process, and final inspection of Orthofix subassemblies and finished products. Perform receiving inspection on incoming materials. Read, comprehend, and follow inspection procedures, drawings, sampling plans, and workmanship standards. Perform in-process and final inspection of subassemblies and finished products. Adhere to FDA/ISO requirements, safety, and corporate policies. | 7/21/2019 |
| 14599 | Osmothica Pharmaceuticals Marietta, GA Validation Engineer BS/BA in engineering Exp: 1-3 years in validation |
The Validation Engineer is responsible for supporting validation activities pertaining to new and existing cGMP systems including process equipment, utilities, cleaning, and computer systems according to current Good Manufacturing Practices (cGMP). The validation activities will include but are not limited to measuring, analyzing, and calibrating equipment and processes to ensure all cGMP systems and equipment are operating according to the predefined specifications and the output of the systems or equipment are consistently and reliably meeting the needs of the user. | 7/21/2019 |
| 14600 | Atsuka Princeton, NJ Associate, Regulatory Affairs BS/BA in life sciences or related Exp: 0-2 years in pharma/regulatory |
The Associate, Regulatory Affairs assists the regulatory representative to Project Teams for assigned projects or products and by providing regulatory tactical support and strategy under guidance from manager. Ensures that clinical trials meet regulatory requirements as designed. Prepares and ensures rapid and timely submission of new drugs and maintain applications to sustain approved status of marketed drug in conjunction with more senior members of the department. | 7/21/2019 |
| 14601 | Lentigen Technology Gaithersburg, MD Research and Development Scientist I (HIV) MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to perform duties within the area of infectious disease research and development. This includes genetic manipulation of viral vectors, immune cells and working with live HIV-1 as it relates to HIV Immunotherapy. Furthermore, you will be responsible for designing specific experiments relevant to HIV Immunotherapy and analyzing the data using appropriate statistical methods. | 7/21/2019 |
| 14602 | Lentigen Technology Gaithersburg, MD R&D Molecular Biology Associate MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology Research and Development team, you will have the exciting opportunity to play a key, hands-on role within the functional area of molecular/synthetic biology and immunology as it relates to the creation of lentiviral gene vectors. More specifically, you will use Lentigen’s expertise in lentiviral vector technology to analyze the biology of immune effector cells, stem cells and immortalized cell lines modified by lentiviral transduction. | 7/21/2019 |
| 14603 | Miltenyi Biotech Sunnyvale, CA Manufacturing Associate BS in biological sciences or related Exp: 1-3 years in clinical processing/cell culture |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. | 7/21/2019 |
| 14604 | Miltenyi Biotech Auburn, CA Logistics Associate HS Diploma/GED Exp: 1 or more year related |
You will prepare and process inventory using your Enterprise Resource Planning (ERP) and shipping systems knowledge. In addition, you will record and receive incoming shipments according to established SOPs, as well as prepare and process shipments according to international regulations. There will also be occasion for employing hand-trucks and forklifts in order to move and store certain articles during routine inventory maintenance. | 7/21/2019 |
| 14605 | Miltenyi Biotech Auburn, CA Accounting Associate AS/AA Exp: 1-3 years in corporate business/accounting |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. | 7/21/2019 |
| 14606 | Pace Analytical Fort Dodge, IA Microbiology Lab Technician BS in microbiology or related Exp: 0-2 years lab experience |
This candidate will be supporting research and development of vaccines in animal care products. They will be responsible for equipment and media prep. Sterilization of equipment. Tear down and clean up of lab set-up. Preparation and sterilization of equipment and supplies. Prepare media and solutions. General microbiology tests including as needed | 7/21/2019 |
| 14607 | Pace Analytical Indianapolis, IN Chemist - QA Validation BS/BA Exp: 0-5 years lab experience |
This individual's primary responsibility is to perform analytical methods and validations in order to find exceptions on the instrument and/or software side. They will be responsible for executing validation documentation on a variety of instrumentation in a pharmaceutical setting. Pharmaceutical and GMP experience is preferred, but candidates with experience with instrumentation in a regulated environment are highly encouraged to apply. | 7/21/2019 |
| 14608 | Pace Analytical Maplewood, MN Physical Properties Technician BS/BA in chemistry, physics, material sciences or related Exp: 0-2 years, recent graduate |
The Physical Properties Technician will perform routine testing/characterization on a drug delivery device in a GMP laboratory setting. Perform physical properties characterization on a medical device such as appearance, adhesion, and performance. Perform wet chemistry as needed and properly dispose of samples and reagents. Operate instrumentation such as FTIR, microscopes, and other dimensional analysis tools | 7/21/2019 |
| 14609 | Pace Analytical New Castle, DE Entry-Level Chemist BS/BA in chemistry or engineering Exp: 0-2 years |
Responsible for performing inspections and laboratory analysis utilizing a variety of techniques, to ensure quality of production. This includes quality checks of raw materials used in the production process to ensure they meet ISO standards; quality checks of production samples and final products prior to shipment to the customer. This includes transferring clear and accurate data from all laboratory analyses performed to the appropriate department. | 7/21/2019 |
| 14610 | Pace Analytical Philadelphia, PA Entry-Level Chemist BS/BA in chemistry or engineering Exp: 0-2 years |
Responsible for performing inspections and laboratory analysis utilizing a variety of techniques, to ensure quality of production. This includes quality checks of raw materials used in the production process to ensure they meet ISO standards; quality checks of production samples and final products prior to shipment to the customer. This includes transferring clear and accurate data from all laboratory analyses performed to the appropriate department. | 7/21/2019 |
| 14611 | Pace Analytical Philadelphia, PA Entry-Level Chemist BS/BA in chemistry or engineering Exp: 0-2 years |
Responsible for performing inspections and laboratory analysis utilizing a variety of techniques, to ensure quality of production. This includes quality checks of raw materials used in the production process to ensure they meet ISO standards; quality checks of production samples and final products prior to shipment to the customer. This includes transferring clear and accurate data from all laboratory analyses performed to the appropriate department. | 7/21/2019 |
| 14612 | PACT Pharma South San Francisco, CA QC Associate MS/MA Exp: 1+ year in QC |
Highly experienced in an analytical development and/or QC laboratory with a track record of successful development of PCR-based, ELISA-based, and/or flow cytometry-based methods for GMP and GLP use, including creating analytical development plans and experiment design, generation of test procedures, qualification/validation, and establishing product specifications and critical quality attributes and limits. | 7/21/2019 |
| 14613 | Pandion Therapeutics Cambridge, MA Associate Scientist, Protein Purification & Characterization BS or MS in life sciences/chemistry Exp: 1-5 years experience |
Perform expression and purification of antibodies, Fc-fusion proteins and recombinant proteins. Perform basic protein QC to determine purity and homogeneity. Conduct protein characterization in binding, polyreactivity and chemical/physical stability studies. Thoroughly document experiments and communicate results across Program Teams. Present scientific data within and across Program Teams | 7/21/2019 |
| 14614 | AMRI Albuquerque, NM Packaging Process Technician HS Diploma/GED Exp: 3 months |
The Packaging Process Technician will provide quality oversight to the packaging processes and functions during the inspection and cartoning of commercial product lots. Direct support and oversight will be provided to internal departments to ensure compliance of cGMP standards and FDA regulations. Additionally, the Packaging Process Technician will perform real time review and approval of PBRs and supporting documentation accompanying the packaging processes and work with appropriate Line leads/Supervisors to ensure documentation errors or issues are resolved. | 7/21/2019 |
| 14615 | AMRI Albany, NY Research Scientist I - Fermentation & Biocatalysis BS/BA in biomedical engineering/biology/biochemistry Exp: 0-2 years |
The Research Scientist is an integral part of the AMRI team, contributing to our success by the cultivation of microorganisms; the screening of biocatalysts and process conditions; and the production, isolation, purification, and analysis of the products of fermentation and/or biochemical transformation. | 7/21/2019 |
| 14616 | Par Pharmaceuticals Chestnut Ridge, NY Primarily responsible for processing, analyzing, negotiating and collecting disputes related to quarterly Medicaid Rebates for approximately 2,000 pro BS/BA in finance, accounting, economics, or math Exp: 1-3 years internships/professional experience |
Primarily responsible for processing, analyzing, negotiating and collecting disputes related to quarterly Medicaid Rebates for approximately 2,000 products and 51 state entities for 8 Labeler codes for a total of 1, 227 quarterly invoices (shared with approximately 8 other analysts). | 7/21/2019 |
| 14617 | Par Pharmaceuticals Chestnut Ridge, NY Quality Associate l HS Diploma/GED Exp: 0-1 years |
The Quality Associate I, Operations is responsible for actively participating in “on the floor” Quality activities during product manufacturing and/or packaging. Quality activities include product sampling and inspection, area clearance to confirm process readiness, and non-conforming event support to resolve in-process issues. Identifies and escalates issues or problems to appropriate supervision. | 7/21/2019 |
| 14618 | Par Pharmaceuticals Chestnut Ridge, NY Quality Associate I - 2nd Shift HS Diploma/GED Exp: 0-1 years |
The Quality Associate I, Operations is responsible for actively participating in “on the floor” Quality activities during product manufacturing and/or packaging. Quality activities include product sampling and inspection, area clearance to confirm process readiness, and non-conforming event support to resolve in-process issues. Communicates to multiple departments and supervision to provide timely process and issue updates | 7/21/2019 |
| 14619 | Par Pharmaceuticals Chestnut Ridge, NY Manufacturing Operator HS Diploma/GED Exp: 0-2 years |
The Manufacturing Operator I performs functions relating to the processing of drug products, ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements and in conjunction with all Standard Operating Procedures (SOPs). Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. Learns to apply skills and knowledge to recognize issues and to increase efficiency, throughput and quality. Learns, understands and runs processes to meet the assigned standards/routers and fulfills the assigned schedule; when these are not achieved, may participate in the debrief to understand the reasons why and what needs to be corrected moving forward. | 7/21/2019 |
| 14620 | Par Pharmaceuticals Irvine, CA Warehouse Operator I HS Diploma/GED Exp: 0-1 years |
Learns to receive components and supplies, pulling orders, issuing and returning components, shipping product, assisting with inventory, and maintaining warehouse cleanliness. Completes tasks with close supervision or oversight. May participate in continuous improvement projects. Interfaces with other departments. | 7/21/2019 |
| 14621 | Nurix San Francisco, CA Temporary Research Associate I/II BS or MS in life sciences Exp: 0-5 years |
We are seeking a talented and highly motivated scientist to join our Library Discovery team and help us augment our DNA encoded library collection. DEL synthesis requires a hybrid of techniques that are borrowed from chemistry environments: chemical reaction setup, LCMS analysis, SAR evaluation, split and pool library synthesis workflows, parallel reaction development, as well as from biology laboratories: aqueous buffer preparation, centrifuge use, ethanol precipitation of DNA, A260 DNA quantification, gel electrophoresis, bioanalyzer analysis, enzymatic DNA ligation. An exposure to some of these techniques is helpful in training into a DNA encoded scientist. | 7/19/2019 |
| 14622 | NuVasive San Diego, CA Assoc. Development Engineer, Surgical Instruments BS in mechanical engineering or related Exp: 0-2 years |
Technical activities include projects leading to product improvement. You will also contribute on several levels including: Complete engineering models and drawings of Customized Instruments. Contribute documentation for support of Customized Instrument Design History Files. Perform quality inspection of finished devices . Interface effectively with internal and external suppliers and become educated on manufacturing methods and capabilities. | 7/19/2019 |
| 14623 | NuVasive Raleigh , NC Development Engineer BS in mechanical engineering or related Exp: 1-3 years previous experience |
Technical activities include projects leading to product improvement. You will also contribute on several levels including: Contribute documentation for support of project Design History Files. Gain cadaver lab/OR experience – support Surgeon training. Interface effectively with suppliers and become educated on manufacturing methods and capabilities. Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485 | 7/19/2019 |
| 14624 | NuVasive San Diego, CA Clinical Research Associate BS in life sciences, biological sciences, or related Exp: 1-3 years in clinical trials |
The CRA is responsible for fulfillment of all clinical research objectives in support of product validation and ongoing verification of product safety and performance in pursuit of clinical data compliance to MEDDEV 2.7/1 rev. 4 and EU MDR. Largely site management and field-based site monitoring with additional study responsibilities as required by team. | 7/19/2019 |
| 14625 | Obsidian Therapeutics Cambridge, MA Research Associate/Senior Research Associate: Gene Delivery BS/MS Exp: 1+ years in biotech/pharma industry |
Maintain cell cultures and cell banks; produce, concentrate, and characterize lentiviral, retroviral, and non-viral vectors for gene delivery into cell lines and primary cells. Organize and execute laboratory experiments, according to high scientific standards. Work with project teams to collect and prioritize production requests; organize and maintain inventory of lentiviral and retroviral stocks. Maintain accurate and detailed laboratory notebook and documentation. | 7/19/2019 |
| 14626 | Ology Bioservices Alachua, FL Lab Tech I BS/BA in biochemistry, chemical engineering, microbiology or related Exp: 0-2 years |
The Downstream Pilot Plant Technician I reports to Downstream Pilot Plant Manager and performs method development, product and process development, scale up/scale down processing and purification, performing a wide variety of activities including but not limited to the following: Basic cell and tissue culture of prokaryotic and eukaryotic systems. Expression and purification of recombinant proteins using a variety of expression systems. General analytical chemistry, protein biochemistry and molecular biology methods such as liquid chromatography (HPLC, FPLC and low pressure systems), gel electrophoresis, western blotting, ELISA, PCR, protein assays, enzyme/bioactivity assays and bioinformatics. | 7/19/2019 |
| 14627 | Olympus Minneapolis, MN Endoscopy Support Specialist I BS/BA and or clinical experience Exp: 1+ in sales/services |
The Endoscopy Support Specialist I maintains responsibility will be to obtain core Olympus product, service and operational knowledge during initial training period. He/ She must successfully complete specialized customer service training to develop customer relationship building skills to provide customer endoscopy support activities, successfully attend and complete a structured training curriculum which will include classroom instruction and hands on equipment practice and evaluation. The Endoscopy Support Specialist l will also learn and implement repair service strategies within a discreet territory that will provide customer assistance in reducing service contract costs, support service contract renewals and create opportunities to increase repair service market share. | 7/19/2019 |
| 14628 | Olympus State College, PA Transducer Designer Engineer I BS/BA in mechanical/materials engineering Exp: 0-2 years |
The Transducer Design Engineer performs engineering design, development, and maintenance tasks, and assist in various phases of ongoing projects. He / She works with a dynamic team of product managers, mechanical, acoustical and manufacturing engineers to improve existing and create new best-in-class single-element and phased array probes. The incumbent's work includes concept generation, CAD layouts, detail design, fixture design and testing. | 7/19/2019 |
| 14629 | Olympus Fort Worth, TX Technical Sales Representitive I BS/BA in technical or business discipline Exp: 1+ years in high end capital equipment sales |
You will spend time creating a complete solution for customers across a wide variety of industries and applications. Your expertise in product applications, equipment demonstrations, and creating a value proposition is critical for our customers. You must have an entrepreneurial drive to target, educate, and persuade customers to use Olympus innovative product solutions. You will know when and how to introduce other Olympus technical experts and industry specialists to our customers as part of your strategy to win. | 7/19/2019 |
| 14630 | Olympus New York City, NY Imaging Sales Associate BS/BA in biomedical/life sciences Exp: 1+ years |
The Associate Imaging Representative (confocal) functions as a resource for the customer. Identify customer needs based upon detailed discussions. Using product and application knowledge, provide solutions to meet their imaging and system needs. Install and train customer using equipment purchased. | 7/19/2019 |
| 14631 | Olympus Albany, NY Microscopy Sales Associate BS/BA in biomedical/life sciences Exp: 1+ years |
The Microscopy Sales Associate functions as a resource for the customer and identifies customer needs based upon detailed discussions. Using product and application knowledge, the incumbent provides solutions to meet their needs. He/She also installs and trains customer using equipment purchased. | 7/19/2019 |
| 14632 | Olympus San Jose, CA Regulatory Affairs Analyst I BS/BA in scientific discipline Exp: 1+ year in complaint handling in related field |
The Regulatory Affairs Analyst I is responsible for the review and investigation of medical device complaints. The incumebent coordinates the resolution of complaints and ensures that timely investigations are performed. He/She prepares and files Medical Device Report (MDR) for Medical Systems Group (MSG) products. The RA Analyst I maintains quality documents to ensure compliance with FDA regulations and guidance documents relating to these areas of responsibility. The incumbent functions as part of MSGs Regulatory Affairs team, in fulfillment of corporate objectives for FDA regulatory compliance. He/She requires general instruction for routine assignments, from Supervisor and/or more experienced staff. | 7/19/2019 |
| 14633 | Olympus Richmond Hill, On Endoscope Technician I HS Diploma Exp: 0-1 years in technical repairs |
The OCI Endoscope Technician I must understand and accept the responsibility to ensure the safety of all Olympus products that are repaired, by following established processes and procedures. The incumbent shall evaluate, troubleshoot, disassemble, assemble, repair and/or inspect Endoscopes, Electronics, or Microscopy products to assure proper function. | 7/19/2019 |
| 14634 | ThermoFisher Austin, TX Data Analyst BS/BA in technical field Exp: 1-3 years in data analystics |
By supporting the Product Quality function within CMD, you will help us achieve product quality improvement goals ultimately leading to increased customer satisfaction and product margins. Primary responsibilities will be improving data quality & reporting formats, developing quality checks to ensure correct reporting, and creating dashboards supporting all product quality metrics. Additionally, this role will support any data analyses required by CMD Product Quality Team. | 7/19/2019 |
| 14635 | ThermoFisher Lenexa, KS Technician I HS Diploma Exp: 1-2 years in QC/QA, microbiology lab, etc. |
Review and maintain product compliance specifications, documentation control. Gain proficiency on all technician benches. Documentation of testing results and determination of aesthetic quality on plated finished product. Responsible for maintaining department equipment and ordering consumable stock supplies when necessary. Work closely with Quality Assurance department as a quality team. | 7/19/2019 |
| 14636 | ThermoFisher Greenville, SC Formulation Technician II HS Diploma Exp: 1+ year in manufacturing/production |
Sets-up, operates, and maintains the classified environments and manufacturing equipment for pharmaceutical products. Requires proficiency in; cleaning and sterilizing equipment, gowning and aseptic techniques, preparing equipment and components for operations, operating and troubleshooting mechanical equipment, following approved procedures and proper documentation. | 7/19/2019 |
| 14637 | ThermoFisher Cambridge, MA Lab Support Technician AS/AA or BS/BA Exp: 1-3 years related experience |
This position is focused on service delivery excellence for UnityTM Lab Services. Specific activities relative to the job function could include: Support of large molecule Scale Up lab activities, including working with cell lines, experiment protocol execution, Media and buffer preparation, lab ware processing, and equipment standardization support. This position will utilize the basic functionality of systems and applications relevant to the job function. Strong communication skills are also required. | 7/19/2019 |
| 14638 | ThermoFisher Branford, CN Software Engineer I BS in computer science or engineering Exp: 1-3 years Java development |
The Digital Science group of Thermo Fisher Science, located in Branford, Connecticut is seeking a highly-motivated individual who will be participating in all phases of product development in our mission to build a large, distributed web-based platform that scales and adapts to a variety of scientific, medical, and laboratory needs. Codes software applications to adhere to designs supporting internal business requirements and external customers. Design, build, and maintain efficient, well designed, and testable code | 7/19/2019 |
| 14639 | ThermoFisher St. Louis, MO Biopharmaceutical Technician I - Days AS/AA or BS/BA in biology, biochemistry, or chemistry Exp: 1-3 years lab experience |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 7/19/2019 |
| 14640 | ThermoFisher Bend, OR Formulation Technician I AS/AA Exp: 1 or more years production experience |
Maintains cleanliness required of equipment, work areas, and facility with assistance of assigned personnel. Prepares manufacturing suites and components for Production Batch Record execution. Performs cleaning of the cGMP suites. Executes Production Batch Records. Executes Work Orders. Keeps proper Personal Protective Equipment (PPE) and gowning materials supplied in gowning suite. Maintains cGMP materials inventory according to applicable Standard Operating Procedures (SOP’s). Complies with established waste disposal operations. | 7/19/2019 |
| 14641 | Organogenesis La Jolla, CA Manufacturing Associate I - DG Growth BS/BA in biology or related Exp: 0-1 years |
Manufacturing Technician I is responsible for completing and assisting with daily tasks associated with cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Additionally, the Technician I will be responsible for following SOPs, performing daily tasks in a clean room/cGMP environment per the current QSRs. The Manufacturing Technician I may also be responsible for the troubleshooting of manufacturing challenges | 7/19/2019 |
| 14642 | Organogenesis Norwood, MA Production Associate I - Human Tissue Processing Degree in biotechnology or related Exp: 1-3 years relevant experience |
The Human Tissue Processing (HTP) Production Associate I is an entry level position. The HTP Production Associate I will perform the production activities associated with HTP Products, produced at Organogenesis Norwood, with supervision. The associate will adhere to the appropriate SOPs, MBRs, and cGMP procedures in the general lab area as well as the Class 10,000 clean room. The HTP Production Associate I will report to the HTP Supervisor. | 7/19/2019 |
| 14643 | Organogenesis La Jolla, CA Manufacturing Technician - TCS Degree in biotechnology or related Exp: 0-1 years |
The Manufacturing Technician I - TCS is responsible for completing and assisting with daily tasks associated with support related functions for TC including assembly and sterilization of sub-assembly items, material management and manufacturing final product for commercial distribution. Responsible for following SOPs, performing daily tasks in a clean room/cGMP environment per the current QSRs. May also be responsible for troubleshooting manufacturing product challenges. Follows established company rules, regulations and safety precautions, and maintains quality standards | 7/19/2019 |
| 14644 | Organogenesis Multiple Locations, US Tissue Regeneration Associate BS/BA Exp: 0-2 years sales experience |
Responsible for supporting sales growth in specific assigned accounts within a territory or territories. Success is realized by building strong customer relationships primarily through case coverage, conducting consultative sales calls, utilizing current product and disease state technical knowledge, developing and following an account business plan, and reporting sales related activities to management through a call reporting system. This position will be responsible for sales support and case coverage inphysician offices, clinics, hospitals and ambulatory surgery centers in the defined geography. | 7/19/2019 |
| 14645 | Organogenesis Canton, MA Production Associate I - Collagen BS/BA in biology or related Exp: 0-2 years |
The Production Associate I - Collagen performs activities involved in the production of Collagen These activities include, but are not limited to, protein purifications, filtrations, and titrations in the production of high quality, purified, sterile collagen for both internal and external customers. This position requires working in a regulated area under the direct supervision of a team leader or departmental supervisor. | 7/19/2019 |
| 14646 | Organogenesis Norwood, MA QC Analyst I/II - Microbiology BS/BA Exp: 6 months + experience in GMP/Medical Device/Pharma |
The QC Analyst I/II performs quality activities in support of product production and releases. The position has interaction with other internal departments, including Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also has interactions with external entities including contractors and suppliers. The QC Analyst I/II performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, and reporting results. | 7/19/2019 |
| 14647 | Origene Rockville, MD Research Associate –Immunology BS/BA in biology, biochemsitry, or related Exp: 1-2 years work experience |
Involves multiple de novo R/D projects for antibodyand assay products development.Performsvalidation tests on variant sera or antibody samples. Participates other duties such as antibody production, purification and conjugation. Strong organizational skills and possess strong ability to identify, analyze and solve the problems independently. | 7/19/2019 |
| 14648 | Origene Rockville, MD Research Associate–Molecular Biology BS in life sciences Exp: 1+ years |
The qualified candidate will support company’smolecular biology operations,principally performing DNA cloning and molecular biology experiments following protocols. Perform experimentsfollowing protocols for plasmid DNA purification, DNA digestion, gel electrophoresis,DNA fragment purification, ligation, transformation, DNA quantitation,DNA sequencing,PCRand cell culture | 7/19/2019 |
| 14649 | OpGen Gaithersburg, MD Clinical Lab Scientist II BS in related sciences Exp: 0-1 year lab experience |
The Clinical Laboratory Scientist II will work within the Clinical Laboratory to perform pre-analytic and post-analytical testing. Clinical Laboratory Scientist may be required to perform validation testing for protocol improvement within the department or testing related to research and development. | 7/19/2019 |
| 14650 | NuVasive San Diego, CA Assoc. Test Engineer, Validation MS in computer sciences, engineering or related Exp: 1+ years related experience |
As the Validation Engineer, you will ensure the quality of the medical device software and hardware meets the design requirements and that they are testable. You will also develop, implement and maintain test plans, protocols, test scripts and traceability matrix for design verification & validation. Execute protocols/test scripts and document results. Ensure compliance with FDA device regulatory requirements, including DHF and 510(k). Communicate with Hardware and Software Development, Marketing, Technical Services, and other project team members to ensure schedules and requirements are consistent with project expectations. Maintain design verification and validation documentation in accordance with established departmental and corporate procedures | 7/19/2019 |
| 14651 | NuVasive Memphis, TN Associate Distribution Coordinator HS Diploma Exp: 1+ years related experience |
The Associate Distribution Coordinator initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties: Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Compiles and maintains manual or computerized records such as material inventory, in-process production reports, and status of material locations | 7/19/2019 |
| 14652 | NuVasive San Diego, CA Development Engineer, Product Engineering BS in mechanical engineering or related Exp: 1-3 years previous experience |
Technical activities include projects leading to product improvement. You will also contribute on several levels including: Contribute documentation for support of project Design History Files. Gain cadaver lab/OR experience – support Surgeon training. Interface effectively with suppliers and become educated on manufacturing methods and capabilities. Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485 | 7/19/2019 |
| 14653 | NuVasive San Diego, CA Development Engineer BS in mechanical engineering or related Exp: 1-3 years |
Technical activities include projects leading to product improvement. You will also contribute on several levels including: Contribute documentation for support of project Design History Files. Gain cadaver lab/OR experience – support Surgeon training. Interface effectively with suppliers and become educated on manufacturing methods and capabilities. Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485 | 7/19/2019 |
| 14654 | Smiths Medical Southington, CT 3rd Shift Team Technician HS Diploma/AS Exp: 1-2 years |
The Team Technician is responsible for ensuring the correct operation of automatic and semi-automatic assembly production equipment in accordance with governing documentation. This person will also initiate action to prevent the occurrence of nonconformances related to the product and equipment. Additionally, this role will identify and record problems relating to the product, process and or quality system. The Team Technician will also initiate recommendations, provide solutions, and verify the affectivity of continuous operational improvements. etc. | 7/16/2019 |
| 14655 | Smiths Medical Minneapolis, MN Finacial Analyst MBA Exp: 1-2 years |
The Financial Analyst will provide financial and commercial decision support. The individual holding this role will be required, with some guidance, to monitor the financial impact of his/her business function against plan and provide reliable and timely analysis to guide the business leaders in their decision-making process. Duties & Responsibilities: Provides financial support to the business function, under guidance of the Business Partner, or Regional Business Partner. Supports the annual budgeting and forecasting processes. Monitors key performance indicators and interprets financial and operational performance. etc. | 7/16/2019 |
| 14656 | Smiths Medical Dublin, OH Group Leader - Airway 2nd Shift (2:30pm - 11pm) HS diploma or equivalent Exp: 1-2 years |
The Group Leader is responsible for successfully leading the department’s day-to-day activities (people/equipment/processes) with regards to safety, quality, customers, and efficiencies. Duties & Responsibilities: Demonstrate leadership and accountability in providing and sustaining a positive safety culture. Provide support for safety training, meetings, and programs. Provide recognition for safe behavior through position observations. Ensure proper instruction is provided on responsibilities and safe job performance (on the job training). Provide support for safety training, meetings, and programs. etc. | 7/16/2019 |
| 14657 | Smiths Medical Dublin, OH Group Leader - Auto Assembly 3rd Shift (10:30pm-7am) HS diploma or equivalent Exp: 1-2 years |
The Group Leader is responsible for successfully leading the department’s day-to-day activities (people/equipment/processes) with regards to safety, quality, customers, and efficiencies. Duties & Responsibilities: Demonstrate leadership and accountability in providing and sustaining a positive safety culture. Provide support for safety training, meetings, and programs. Provide recognition for safe behavior through position observations. Ensure proper instruction is provided on responsibilities and safe job performance (on the job training). Provide support for safety training, meetings, and programs. etc. | 7/16/2019 |
| 14658 | Smiths Medical Southington, CT Mechanical Engineer II - Medical Device Advanced degree in engineering Exp: 1-2 years |
Smiths Medical is currently hiring a Mechanical Engineer II in Southington, CT. The Mechanical Engineer II will be responsible for product and component detail design, creation of 3D models and product drawings with proper GD&T, development and delivery of Design Verification activities (test method development/fixture design/DV plans/test protocols/reports). Duties & Responsibilities: Performs engineering work requiring full competency in all conventional aspects of engineering. Plans and conducts work requiring judgment in the independent evaluation, selection and the substantial adaption of standard engineering techniques, procedures and requirements. Plans and coordinates detailed phases of engineering actions for part of a project. Conducts engineering activities of intermediate scope or degree of difficulty. This could include medium – large components/system, processes associated with a medium or large project. etc. | 7/16/2019 |
| 14659 | Smiths Medical Minneapolis, MN Office Associate, Facilities HS diploma Exp: 1-3 years |
Position’s primary role is that of First Impressions Coordinator: Greeting and coordinating credentials for guests and their hosts within Smiths Medical. They also play a role in meeting site security and facility needs. They act as site concierge for all guests and employees. Supports catering activities and conference room bookings. Associate will also provide back-up for the Mail Room Associate. Position reports to Facilities Manager. Duties & Responsibilities: Welcomes visitors by greeting them, in person or on the telephone; answering or referring inquiries. Directs visitors by maintaining employee and department directories; giving instructions. Maintains security by following procedures; monitoring logbook; issuing visitor badges. etc. | 7/16/2019 |
| 14660 | Smiths Medical Minneapolis, MN Product Surveillance Complaints Coordinator II BS/BA Exp: 1 year |
The Product Surveillance Coordinator II role contributes to the process of timely, high quality and consistent product complaints management, including appropriate identification and response to risks, adverse event reporting decisions, and collection and documentation of complaints. Duties & Responsibilities: Set up and manage product complaints in the global complaints database to ensure complaints are managed according to regulatory requirements and customer expectations. Communicate with customers, Affiliates and internal departments regarding product complaints and document the complaint file. Use judgment to analyze adverse event information and determine if events are reportable to regulators. etc. | 7/16/2019 |
| 14661 | Solid Biosciences unspecified, Staff Accountant BA/BA in accounting, finance, or business administration Exp: 1+ years |
The Staff Accountant will support the Controller with all accounting, finance and administrative duties. Key Duties & Responsibilities: Responsible for maintaining the integrity of General Ledger accounts, structure and cost elements. Ensure monthly financial closings are in line with expectations (on time and on quality); coordinate GL resources to work according to plan (timetable, deliverables). Ensure timely and accurate financial reporting to internal/external customers (Controlling, Auditors and others). etc. | 7/16/2019 |
| 14662 | Solid Biosciences unspecified, Staff Accountant/AP Specialist BA/BA in accounting, finance, or business administration Exp: 1+ years |
Solid Biosciences is looking to hire a proactive and dedicated Staff Accountant/AP Specialist to join our fast-paced Finance team. In this position, you will be responsible for the accounts payable process and assisting with the accounting close process. Key Duties & Accountabilities: Accurately process/input invoice information in G/L system and route invoices for approval to the business. Work on vendor statements. Monitor the AP inbox and respond to inquiries. etc. | 7/16/2019 |
| 14663 | SomaLogic Boulder, CO Bioinformatics Analyst II/III/Sr 2019-113 MS in computer science, statistics, mathematics, biochemistry, molecular biology, genetics, or related Exp: No experience for Master's degree |
Key Job Responsibilities: Conduct routine analysis on collaborator data as it is generated by the service lab, applying standard quality assessment protocols, and providing results to collaborators. Use internally developed and off the shelf tools to process collaborator data into standard results. Apply standard quality assessment protocols to results generated and coordinate with laboratory personnel regarding assay quality and protocol deviations. Monitor and manage data flow for collaborator samples, providing regular feedback to project management. Participate in study planning calls with collaborators to discuss how their samples will be analyzed and provide recommendations based on documented best practices. etc. | 7/16/2019 |
| 14664 | Sorrento Therapeutics San Diego, CA Manufacturing Associate BS in biology, biomedical science, chemical engineering, or related Exp: No experience for Bachelor's degree |
A Manufacturing Associate who will be responsible for manufacturing CAR-T cells per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. THE DAY-T0-DAY WORK INCLUDES: Weigh and measures in-process materials to ensure proper quantities are added/removed. Adheres to the production schedule ensuring on-time, internal production logistics. Records production data and information in a clear, concise, format according to proper GDPs. etc. | 7/16/2019 |
| 14665 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I BS in life science, chemistry, or chemical engineering Exp: 1-3 years |
WHAT WE ARE LOOKING FOR: We are looking for enthusiastic and talented individuals who thrive on challenge and change, who can roll up their sleeves, put on multiple hats and have a can-do attitude without a lot of oversight or instruction. We are currently seeking a Manufacturing Associate who will be responsible for performing Upstream manufacturing tasks. Including but not limited to: Tracking & control of raw material inventory. Maintenance and operation of equipment in cGMP facilities. Preparation of buffer and media. Assistance in operation of single use bioreactors for production of clinical and commercial products. | 7/16/2019 |
| 14666 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I BS in life science, chemistry, or chemical engineering Exp: 1-3 years |
WHAT WE ARE LOOKING FOR: We are looking for enthusiastic and talented individuals who thrive on challenge and change, who can roll up their sleeves, put on multiple hats and have a can-do attitude without a lot of oversight or instruction. We are currently seeking a Manufacturing Associate who will be responsible for performing Upstream manufacturing tasks. Including but not limited to: Tracking & control of raw material inventory. Maintenance and operation of equipment in cGMP facilities. Preparation of buffer and media. Assistance in operation of single use bioreactors for production of clinical and commercial products. | 7/16/2019 |
| 14667 | Sorrento Therapeutics San Diego, CA Manufacturing Associate, Downstream BS in life science, chemistry, or chemical engineering Exp: 1-3 years |
We are currently seeking a Manufacturing Associate responsible for performing downstream manufacturing tasks including 1) tracking and control of raw material inventory 2) maintenance and operation of equipment in cGMP facilities, 3) buffer preparation, 4) assist in setup and operation of purification equipment for production of clinical and commercial products. etc. | 7/16/2019 |
| 14668 | Sorrento Therapeutics San Diego, CA Research Associate BS/MS in chemistry, biochemistry, chemical/biochemical engineering or related Exp: 0-3 years |
The Research Associate in our Nanoformulation group is responsible for providing analytical chemistry support to research, process development, product development. This position participates in analytical method development, characterization, qualification, validation as well as method transfer. Laboratory experience in an industrial setting is desired, though applications from both recent graduates and those with more experience are welcome A sound foundation in experimental design, biochemistry, and chemistry is desired along with an ability to troubleshoot issues effectively. etc. | 7/16/2019 |
| 14669 | Sorrento Therapeutics San Diego, CA QC Associate BS in microbiology Exp: 1-2 years |
This individual contributes to general operations and testing for the Quality Control and Microbiology Laboratories. This position supports in-process testing and drug substance and drug product release and stability testing programs. Works independently under general supervision. ESSENTIAL DUTIES AND RESPONSIBILITIES: Routine Environmental Monitoring in aseptic manufacturing environment” active air sampling, non-variable particulate monitoring, surface and personnel sampling. Incubation and counting of plates. Bae knowledge of microbial organisms and microbiological techniques. etc. | 7/16/2019 |
| 14670 | Spark Therapeutics Philadelphia, PA Flow Cytometry Specialist BS/MS in biological sciences Exp: 1-4 years |
The Flow Cytometry Specialist will: Contribute to the advancement of gene therapy initiatives by developing, optimizing, validating and performing flow cytometry analyses on clinical, pre-clinical, and R&D samples utilizing in-depth knowledge of flow cytometric techniques. Perform complex data analyses and prepare reports and presentations to covey results and novel findings. Design antibody panels for flow cytometry analyses. Assist fellow scientists with flow cytometry experimental design, experimental setup, data acquisition, and data analysis. Train scientists in flow cytometry techniques, methods, instrumentation, etc. Maintain flow cytometry equipment. etc. | 7/16/2019 |
| 14671 | Spark Therapeutics Philadelphia, PA Cell Banking Associate BA/BS in biological sciences Exp: 1-3 years |
The Scientist will: Cell banking and quality testing of prepared batches. Isolation and cryopreservation of PBMCs in the context of clinical and pre-clinical studies. Maintain cell culture facility and culture cell lines as required for experiments including but not limited to: cell expansion, cell feeding, harvesting, counting and freezing. Participate in sample management activities such as receiving, processing, storage and shipping of clinical and preclinical samples. Participate in instrument maintenance and qualification. Maintain accurate, timely and detailed records of work. With guidance and supervision from the supervisor, conduct clinical and preclinical sample analysis per SOPs and generate data with high scientific quality to meet GLP regulatory expectations. etc. | 7/16/2019 |
| 14672 | Spectrum Pharmaceuticals Irvine, CA Temporary- Biostatistician BS/MS in statistics or related Exp: 0-2 years |
The position provides statistical services including analysis, analysis QC, interpretation, design, and reporting or communication of data evidence for research, development, and/or marketed drugs, devices or biologics. Activities associated with the role will require varying levels of guidance from managers and project statisticians. Primary activities include assisting senior level statisticians in reviewing data, performing analysis, QC of analysis and interpretation of the analysis. The person is expected to review all clinical trial and statistical documents such as protocol, statistical analysis plan in order to perform his/her activities. etc. | 7/16/2019 |
| 14673 | Spherotech Lake Forest, IL Technical Customer Support Representative BA/BS Exp: Recent graduate |
Spherotech, Inc. seeks a college graduate for a Technical Customer Support Representative opening. Duties include, but are not limited to providing customer/technical assistance and Microparticle application support. Responsibilities also include representing the company through trade shows, technical publications, and presentations. Required laboratory skills include: Analysis of Microparticles using particle sizers, flow cytometry, fluorescence spectrophotometry, and microscopy. | 7/16/2019 |
| 14674 | Spherotech Lake Forest, IL Manufacturing Associate BS in chemistry or relateed Exp: Recent graduate |
Spherotech, Inc. seeks a college graduate for a Manufacturing Associate opening. Duties include polymer synthesis, bottling, packaging, documentation, etc. This position requires a Bachelor's degree in Chemistry or related field. We offer excellent benefits including paid vacation, health insurance, dental insurance etc. Compensation commensurate with experience. | 7/16/2019 |
| 14675 | Spherotech Lake Forest, IL Quality Control Associate BS in chemistry or relateed Exp: 1+ years |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. This position requires a Bachelor's degree in Chemistry or related field and a minimum of 1 year of experience. We offer excellent benefits including paid vacation, health insurance, dental insurance, etc. Compensation commensurate with experience. | 7/16/2019 |
| 14676 | SQZ Biotech Watertown, MA Research Associate, Analytical Development BS/MS in life science or related Exp: 1+ years |
SQZ Biotechnologies is seeking a flexible, detail oriented analytical thinker as a Research Associate to join the Analytical Development & Quality Control (AD&QC) team. The successful candidate will work within the internal AD&QC team to develop analytical methodologies for characterization of SQZ Biotechnology’s cell therapy products, support internal testing needs, and work collaboratively with Research and Development teams. The successful candidate will also work with external partners to transfer and qualify appropriate test methods. Responsibilities: Contribute to the development of: Flow cytometry methods to characterize cell therapy products, including elucidation of cell composition for blood products, in-process samples and product materials. etc. | 7/16/2019 |
| 14677 | SQZ Biotech Watertown, MA Research Associate, Immunology BS/MS in biology, immunology, or related Exp: 1+ years |
SQZ Biotechnologies is looking for a highly motivated, collaborative, and dynamic Research Associate for our Immunology team within R&D. This role is an opportunity to focus on developing novel immunotherapies for the treatment of cancer. The scope of this work will encompass the design and execution of in vitro and in vivo experiments for internally- and externally-focused research programs. This position requires effective collaboration across multiple groups and the regular presentation of scientific results to multidisciplinary teams. etc. | 7/16/2019 |
| 14678 | STAAR Surgical Monrovia, CA Production Operator I HS diploma or equivalent Exp: 1-2 years |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: Thorough knowledge and appropriate implementation of basic production functions. Completes required production documentation accurately. Consistently meets quality and productivity targets. Appropriately follows company policies, rules, and regulations. Be able to interact well with others and work in a team environment. Maintain work area environment in a clean and orderly manner. Operate production related equipment. Other duties as assigned. | 7/16/2019 |
| 14679 | STAAR Surgical Monrovia, CA Production Technician HS diploma or equivalent Exp: 1-2 years |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: Thorough knowledge of all applicable SOP's: makes proper decisions in line with applicable SOPs and standards under normal conditions. Perform highly technical tasks in support of manufacturing including equipment set-up and manufacturing of product, tool changes, sterilization processes, and filtration of material and calibration activities as assigned. Troubleshoot issues on equipment and assist with preventative maintenance. Edit equipment programs (as required). Assist in revising procedures related to operation and preventative maintenance. Support qualification activities (as required). Train production operators in the processes. Other duties as assigned. etc. | 7/16/2019 |
| 14680 | Smith & Nephew Memphis, TN Material Quality Tech I AS or equivalent Exp: 0-2 years |
The Materials Quality Technician I is responsible for overseeing, and maintaining the laboratory equipment and area. The Materials Quality Technician I is responsible for site-wide compliance of the activities related to Materials. The Materials Quality Technician I will be interacting on a daily basis with Quality and Manufacturing Engineers and Managers. Must be able to convey laboratory practices, policies, and procedures to regulatory bodies such as FDA and notified bodies. The Materials Quality Technician I will have the training and knowledge necessary to perform the Materials laboratory functions and the administrative functions. The Materials Quality Technician I may be assigned to special projects by the Department Management that is commensurate with their level of experience. etc. | 7/15/2019 |
| 14681 | Smith & Nephew Memphis, TN Machine Maintenance Technician 2 AS in industrial maintenance technology or related Exp: 1 year |
Primarily responsible for repairs and scheduled maintenance of production machines and equipment. Also responsible for fabrication of needed parts and modifications to existing machines and equipment. Assists with training manufacturing associates to do preventive maintenance on applicable machines. Performs repairs on machinery and equipment as necessary. Performs PM’s on all manual equipment. Completes all necessary forms listing work done, parts used, parts needed, time involved, etc. Initiates requirements for machine parts and supplies. Performs installation and setup of new equipment as necessary. Installs and maintains air system. etc. | 7/15/2019 |
| 14682 | Smith & Nephew Memphis, TN Quality Assurance Inspector I HS diploma or equivalent Exp: 0-2 years |
The Quality Assurance Inspector I shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. Essential Responsibilities: Inspect raw materials, components, assembled product, semi-finished product & finished product per inspection procedures/drawings and to print specifications. Utilize attribute and variable measuring equipment/gauges as well as mating parts to determine as found/as left conditions of product. Support the qualification/validation processes for company product. etc. | 7/15/2019 |
| 14683 | Smith & Nephew Minneapolis, MN Receptionist AS/AA preferred Exp: 1-3 years |
Provide administrative support to Facility Manager and general office support to other business processes on site. Manage all aspects of office administration for smooth operation of facilities and comfortable, productive environment. Respond to all assignments and requests timely and efficiently; maintain discretion on all confidential or sensitive matters. Support corporate safety directives, policies and procedures; proactively contribute to wider HSE and housekeeping improvement goals. Uphold culture of camaraderie and employee engagement while promoting appreciation, trust and respect. etc. | 7/15/2019 |
| 14684 | Smith & Nephew Memphis, TN Machinist HS diploma or equivalent Exp: 6 months |
This position requires a person to perform simple set ups and operate manual/CNC equipment to manufacture medical components from raw material in a team based environment. Must be able to comply with all governing rules including S.N.E. policies and procedures and adhere to safety and cleanliness practices in the work place. This position works under close supervision. Essential Duties And Responsibilities: Machine medical components, including but not limited to: Perform simple set ups and operate manual/CNC equipment, including turning, milling, grinding, drilling, tapping, EDM and honing. etc. | 7/15/2019 |
| 14685 | Smith & Nephew Memphis, TN Machinist HS diploma or equivalent Exp: 1+ years |
This position requires a person to set up and operate CNC and manual machinery to manufacture medical components from raw material in a team based environment. Must be able to comply with all governing rules including S.N.E. policies and procedures and adhere to safety and cleanliness practices in the work place. This position works under minimal supervision. ESSENTIAL FUNCTIONS: Position Functions: Machine medical components, including but not limited to: Perform moderate set ups and operate CNC and manual metal fabricating equipment, including turning, milling, grinding, drilling, tapping, EDM and honing. | 7/15/2019 |
| 14686 | Smith & Nephew Memphis, TN Graduate Engineer BS in mechanical, manufacturing, industrial or other engineering Exp: Recent graduate |
Responsible for the development of manufacturing methods to produce advanced technology products. You will work under the direction of either a Sr. Engineer or Manager in the development of new processes, introduction of new products, cost reduction projects, and capital justifications. Interface with Production Supervision, Tool Design, and Tool & Die, and Maintenance with respect to manufacturing method, tooling, and equipment. Establish routings for new products and determines manufacturing cost. Contacts and reviews projects with vendors as necessary. etc. | 7/15/2019 |
| 14687 | Smithers Avanza Smithers Rapra, OH Product Testing Technician HS diploma or equivalent Exp: 1-5 years |
Performs laboratory tests to determine physical characteristics of materials and products for such purposes as quality control, process control or product development by performing essential duties and responsibilities. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform testing in accordance with relevant specification(s). Follow daily work assignments relative to test schedule. Have detailed understanding of test methods and specifications. Be able to perform basic calculations from tests. etc. | 7/15/2019 |
| 14688 | Smithers Avanza Wareham, MA Program Manager BS/BA in business or science discipline Exp: 1-3 years |
Currently, we are seeking a full-time Program Manager to join our talented team. This position will support the needs of the Smithers Viscient organization in Wareham, MA and Snow Camp, NC. Job responsibilities: Manage aspects of planning, scheduling, implementation, follow-up, tracking of program tasks, and prioritization of critical program activities for our clients. Individual collects and accumulates program data from sources within the Laboratory or Organization. Responsible for writing and updating client status reports and other required client‑specific documentation. Work closely with all team members to provide services both internally and externally. etc. | 7/15/2019 |
| 14689 | Smithers Avanza Wareham, MA Assistant Biologist BS in biology or related Exp: 6 months of laboratory experience |
Position is expected to perform a variety of routine tasks in support of the conduct of normal laboratory operations. Further, the individual is expected to assist in coordinating testing requirements with supporting departments (i.e. chemistry staff, Quality Assurance and reporting). Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing Standard Operating Procedures, study-specific protocol procedures and other laboratory assignments related to the testing that the individual is routinely associated with. Incumbent is able to apply a collective set of SOPs in order to assist in fully executing a study protocol. Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. etc. | 7/15/2019 |
| 14690 | Smithers Avanza Wareham, MA Instument Operator BS/MS in chemistry, biochemistry, or related Exp: 1-3 years (BS), 0-2 years (MS) |
The Chemistry Division at Smithers Viscient is looking for an intelligent, highly-motivated individual to operate the LC-MS instruments in support of the Ecotox, Residue, and Product Chemistry Departments. The Chemistry Division focuses on performing the necessary chemistry tests to ensure that future pharmaceuticals, agrichemicals, and industrial chemicals are safe. Our clients and the public trust our scientific judgement in this critical regulatory procedure. All Smithers Viscient team members have a hand in making sure the world is safe. The position will report to the Instrument owner and Study Director in our Residue Chemistry group. The instrument operator will be responsible for operating, troubleshooting, and performing routine maintenance for the LCMS Instruments. etc. | 7/15/2019 |
| 14691 | Smithers Avanza Ravenna, OH Tire Testing Technician HS diploma or equivalent Exp: 1-3 years |
SUMMARY: Checking compliance of products to meet industry or client standards. ESSENTIAL DUTIES AND RESPONSIBILITIES: Sets up, adjusts, and operates laboratory equipment and instruments. Tests samples of manufactured products to verify conformity to specifications. Records test results on standardized forms, and writes test reports describing procedures used. Calibrates laboratory instruments, and mounts tires. Must have good attendance and attitude. Must be able to follow directions well. Must be able to learn quickly. Must follow all safety requirements and procedures. | 7/15/2019 |
| 14692 | Smithers Avanza Smithers Rapra, OH F&M Technician HS diploma or equivalent Exp: 1-3 years |
SUMMARY: With the direction and lead of other Force and Moment staff, prepares and installs candidate tire/wheel assemblies for testing on MTS Flatrac® Tire Test Systems and TMSI On-Level Test Systems. Conducts tests and records results by performing the following duties: Follow safety rules and company policies. Maintains tire inventory records and coordinates all shipping and receiving. Confers with other Flatrac® Technicians or Staff to resolve operational or procedural problems relating to specifications, conditions under which tests are to be conducted, and duration of tests. Coordinates and participates in installing tire/wheel assemblies to be tested, connecting valves, pumps, hydraulic, mechanical, cabling, tubing, power source, and indicating instruments. etc. | 7/15/2019 |
| 14693 | Smithers Avanza Gaithersburg, MD Sample Management Technician BS/BA/AAS in life sciences Exp: 18 months of laboratory experience |
Essential Position Responsibilities: Receive, check-in and dispose of study samples according to established guidelines and SOPs. Complete all appropriate paperwork in a timely fashion. Identify and document all discrepancies between client paperwork, Watson LIMS, and sample vials. Notify sponsor and Project Team of the discrepancies. Assures proper storage conditions for sample types. Accessions specimens using automated and manual systems. Use Watson LIMS to set-up shipments and receive shipment samples. Use Watson LIMS to edit subject ID information and assign custom IDs. Prepare sample disposition notifications. etc. | 7/15/2019 |
| 14694 | NovoBiotic Pharmaceuticals Cambridge, MA Associate Scientist - Microbiologist BS in biology/microbiology Exp: Entry Level |
We are seeking to hire an entry-level microbiologist. The positionwill involveworking with a team of scientists to discover new antibiotics from newly cultured species from soil and marine environments. The work will include special projects as well as daily lab tasks such as reagent prep,record keeping, and equipment maintenance. | 7/14/2019 |
| 14695 | Novo Nordisk Seattle, WA Assistant Animal Technician AALAS or ALAT certified Exp: 1 or more year working with rodents |
Responsible for providing a high level of animal care and husbandry, performing regularly scheduled facility maintenance tasks, and contributing technical assistance to research projects in the NNRC rodent facility. Reports to Manager, Animal Research. Internal relationships include working with Animal Technician, Attending Veterinarian, Lab Operations Specialist, Research Associates and Research Scientists locally and globally. | 7/14/2019 |
| 14696 | Novo Nordisk Clayton , NC Aseptic Filling Technician I - Night Shift Job HS Diploma/GED Exp: 1+ year in manufacturing |
Filling of insulin and media preparations under aseptic conditions and operation of inspection equipment to achieve production goals. Operating, monitoring and controlling equipment, systems and processes associated with the Vial/Cartridge filling and inspection lines. Maintaining aseptic areas and performing sanitizations and environmental monitoring. Assist during equipment maintenance including restoration of lost function, predictive and preventative maintenance | 7/14/2019 |
| 14697 | Novum Las Vegas, NV Phlebotomist (PT) Phlebotomy certified Exp: 1-2 years experience |
The Phlebotomist will perform highly skilled, rapid-draw venipuncture and process collected biological samples according to Standard Operating Procedures (“SOPs”), sample collection and processing instructions; verify, pack and ship samples to appropriate facility. | 7/14/2019 |
| 14698 | Novum Las Vegas, NV Pharmacy Technician AS/AA Exp: 6 months to 1 year training/experience |
The Pharmacy Technician will be responsible for assisting the Pharmacy Manager with all aspects of drug handling and storage to assure drug availability and correct dosing according to the protocol. Responsible for handling the receipt, storage, and return to sponsor along with test articles used in clinical studies. Responsible for maintaining daily records of storage conditions of drugs and refrigerator temperatures. Will prepare dosage forms for clinical investigators and provide general support to the clinical operations department. | 7/14/2019 |
| 14699 | Novum Fargo, ND Superviso, Phlebotomy Phlebotomy certified Exp: 1-2 years supervisory + phlebotomy training/experience |
The Phlebotomy Supervisor will be responsible for supporting study progression according to the study protocol and Standard Operating Procedures (SOPs). Also responsible for supervising the phlebotomy staff; performing rapid venipuctures, processing biological samples and providing proper documentation and verification of the same. Will label and prepare study supplies; ensure lab areas are prepared and cleaned and will review lab and tech instructions prior to study start up. Will perform document and QC documentation of all study activities as assigned. Verify, pack, coordinate and manage sample packaging and shipment/delivery to analytical labs. Will perform practical testing for phlebotomy candidates and work with manager to train and schedule staff. | 7/14/2019 |
| 14700 | Neogen Lincoln, NE Lab Technician AA/AS in sciences Exp: 1-2 years lab experience/training |
Performs laboratory tests and services to support customer data generation through sample processing and DNA extraction. Uses a variety of scientific techniques, instrumentation, and disciplines by performing the following duties: Performs sample and reagent preparation, DNA extraction and isolation, quality analysis prior to genotyping, analysis of reagents for performance, and other related tasks. Assist in the training of new assistants and interns in order to better manage laboratory workload. Proficiency in providing input to the best ways to maximize laboratory efficiency. etc | 7/13/2019 |
| 14701 | Neogen Lansing, MI Laboratory Services Tech BS/BA in sciences Exp: 0-3 years |
The ideal candidate will have a B.S. in a science discipline, good communication skills including customer interaction, strong work ethic and laboratory experience is a plus. The selected candidate will manage the on-line sample analysis request program and log in samples received, analyze samples with Neogen’s test kits, according to kit instructions, generates and analyzes data from a variety of laboratory techniques and analytical instrumentation, calibrate analytical instrumentation and ensure all lab equipment is up to date per ISO requirements, perform tasks essential to maintaining ISO Certification, participate in sample proficiency programs, tabulates and graphs data, and prepares technical reports for senior personnel. | 7/13/2019 |
| 14702 | Neogen Lansing, MI QC Lab Tech HS Diploma Exp: 0-2 years lab experience |
The QC lab technician position requires the candidate to prepare microbiological media and buffers. Other responsibilities include; prepping and cleaning the laboratory for daily use, perform preventative maintenance on equipment, maintain and organize QC retains and meeting goals set by the department. The ideal candidate would have some laboratory experience. | 7/13/2019 |
| 14703 | Neogen Lansing, MI Customer Portal & Complaint Rep HS Diploma/GED Exp: 1-3 years customer service experience |
Establish and maintain customer portals for PO entry and invoicing. Direct contact with customers and work closely with company Data Administrator, IT, Accounting, Customer System Information Manager, and CS Manager to provide requested services from customer. Oversee customer complaint database (CMS) – from entry to resolution. | 7/13/2019 |
| 14704 | Neogen Lexington, KY QC Chemist I BS/BA Exp: 0-2 years related experience |
The ideal candidate will possess a knowledge of instrumentation such as FTIR, HPLC, UV/VIS, and KF to be used in the routine analytical testing of samples supporting incoming raw materials, in-process production, finished product, and validation. The selected candidate will be responsible for performing instrument/method troubleshooting as well as validation, qualification, calibration, and preventative maintenance, and performing investigations on out-of-specification and out-of-trend results. The selected candidate will participate in QA functions of the QCU including document review, room and equipment log review, room cleaning approvals, and other quality functions as assigned by the Director of AS Quality Systems. | 7/13/2019 |
| 14705 | Neogen Lansing , MI Packaging Assistant HS Diploma/GED Exp: 1 month + or training/experience |
Assembles and packages diagnostic test kits used in the food safety industry according to Standard Operating Procedures ensuring accuracy and quality throughout the assembly process. Dispense bulk solutions and blended powders into final product packaging. Complete production paperwork, including quantities produced, scrapped and in-process. | 7/13/2019 |
| 14706 | Neogen Lincoln, NE Lab Technician I BS/BA in sciences Exp: 0-2 years training/experience |
Performs laboratory tests and services to support customer data generation within the platform specific processing lab, through a variety of scientific techniques, instrumentation, and disciplines by performing the following duties: Preforms all duties essential to quality high throughput data generations associated with platform specific technology-including but not limited to assigned primary platform and/or secondary platform(s). Gain and maintain the ability to operate all electronic and robotic equipment essential to primary platform processing. This includes all hand held electronic repeaters, multichannel pipettes along with liquid handling robots. Maintain consistency and quality in lab techniques and procedures within an ever changing and fluid work environment. | 7/13/2019 |
| 14707 | Neovasc Vancover, Ca Engineer II BS/BA in engineering, math or similar Exp: 1-2 years in ISO setting |
Work with Engineering, R&D, and external subcontractors to develop test methods and execute testing used in the verification and validation of designs. This includes the design and fabrication of test jigs and equipment suitable for the characteristics being tested. This also includes the drafting of protocols and reports that adequately summarize the testing performed and are suitable for review by the appropriate regulatory authorities. Participateas part of a team undertaking all phases of the development process –from planning and proof-of-concept activities through to product launch | 7/13/2019 |
| 14708 | Nephron West Columbia, SC Microbiology Analyst I BS in biology, microbiology, or life sciences Exp: 1 or more year in pharma |
Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Demonstrate high proficiency level on tests performed. Additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. | 7/13/2019 |
| 14709 | NeuMoDx Ann Arbor, MI Manufacturing Associate, Labeling and Packaging AS/AA in related field Exp: 1 or more years related experience |
Manufacturing Associate, Labeling and Packaging are required to have a strong knowledge of process development experience, work flow understanding, Labeling Reconciliation, Reading and Understanding Labeling and Packaging Specifications. Carry out work in accordance with defined Quality Management System procedures and be fully supportive of Quality initiatives. Prepare room for staging, packaging, and reconciliation. Assist in maintaining fixtures, packaging tools, packaging instrumentation, such as scanners, scales, etc. in packaging areas. | 7/13/2019 |
| 14710 | NeuMoDx Ann Arbor, MI QC Test Technician, Systems BS/BA in sciences, mechanical or software field Exp: 1+ years in instrument production |
The QC Final Test Technician is responsible for QC testing of final production Instruments. In this position the QC Final Test Technician will assist in maintaining manufacturing equipment, train others, may be asked to contribute to projects, and trained to work in several areas as needed. This role requires a self-starter, with the ability to work independently, understand of departmental goals, and work as a team to achieve those goals within set timelines. Carry out work in accordance with defined Quality Management System procedures and be fully supportive of Quality initiatives. | 7/13/2019 |
| 14711 | Neurocrine San Diego, CA Associate Scientist - HTS BS in biology Exp: 1+ year in lab setting |
he ideal candidate must have outstanding written and verbal communication skills, a strong work ethic, and be able to multitask and prioritize responsibilities. The position requires a working knowledge of many automated components of the HTS platform utilized at Neurocrine. This candidate must be able to independently manage their workload, while simultaneously working with his/her supervisor to provide consistent support to the in vitro team on multiple new target screening and lead optimization campaigns. | 7/13/2019 |
| 14712 | Neuropace Mountain View, CA Manufacturing Engineer BS in mechanical/industrial/manufacturing engineering Exp: 0-4 years |
The Manufacturing Engineer is responsible for supporting all aspects of Manufacturing Operations at NeuroPace. Maintain quality standards in and around manufacturing areas, ensuring a safe work environment for all personnel and helps to develop a culture of accountability, continuous improvement, and collaboration. Write, review, and improve manufacturing procedures and forms in compliance with the quality system, ensuring accuracy and consistency. Collaborate with Manufacturing and Development Engineers to create, review, and maintain manufacturing routers. Including verifying manufacturing labor times are properly calculated. | 7/13/2019 |
| 14713 | NGM Biopharmaceuticals South San Francisco, CA Research Associate- Nonclinical Safety (Temp to Perm) BS in life sciences Exp: 1+ years research experience |
NGM Biopharmaceuticals, Inc. is seeking a highly motivated Research Associate to join our Nonclinical Safety development group. This will be a temp to full time position. Needed skills include: NGM Biopharmaceuticals, Inc. is seeking a highly motivated Research Associate to join our Nonclinical Safety development group. This will be a temp to full time position.. Ability to accurately record data in study files. Excellent interpersonal skills, ability to work collaboratively and develop relationships with key stakeholders | 7/13/2019 |
| 14714 | NGM Biopharmaceuticals South San Francisco, CA Regulatory Operations Senior Associate BS/BA Exp: 1-2 years in pharma regulation/operations |
The Regulatory Operations Senior Associate will be responsible for maintaining timelines, formatting & publishing documents, assembling and building Regulatory eCTD submissions such as original INDs, IND amendments and/or CTAs and overseeing & archiving submissions. All will be done in accordance with and requires knowledge in applicable Regulatory Agency regulations, guidelines, and/or specifications (FDA, EMA, ICH, etc). Responsible for formatting, editing, proofing, bookmarking and internal document hyperlinks according to guidance and internal processes. Troubleshoot and resolve complex document issues. | 7/13/2019 |
| 14715 | Nitto Cincinnati, OH Process Development Chemist BS or MS in chemistry or related Exp: 0-4 years |
Execute chemical processes for preparation and delivery of clinical candidates. Follow instructions in protocols and development batch records. Prepare reagents for chemical processes. Work with process development scientists and team leaders to execute process development experiments. Adhere to all environmental health and safety policies. Establish working relationships with project teams to satisfy demanding process development timelines | 7/13/2019 |
| 14716 | Nkarta Therapeutics South San Francisco, CA Research Associate/Process Engineer MS in biology-related discipline Exp: 1-6 years lab experience |
We are currently offering a unique opportunity for a highly motivated development associate to join our team with development experience in cell therapy. Responsibilities include: Support process development of phase appropriate cell therapy production processes. Evaluate raw materials and culture systems for use in cell therapy manufacturing processes. Support process optimization efforts to increase process robustness, reduce costs and improve yield. Design and execute experiments independently; accurately record, analyze and communicate data to senior staff and team members | 7/13/2019 |
| 14717 | Nordson Salam, NH Production Associate I (Balloon) Third Shift HS Diploma/GED Exp: 0 years |
Position consists of manufacturing of medical components in a clean room environment while under general supervision in accordance with specifications and written procedures. This position may include machine operation, manual production using hand tools, visual inspection, physical measurements, and packaging of finished product. This position requires the ability to work with small and delicate components using a high degree of dexterity and accuracy. This position requires direct contact with medical grade components. | 7/13/2019 |
| 14718 | Nordson Salam, NH Production Associate (Balloon) Third Shift HS Diploma/GED Exp: 0-2 years |
The Operator is responsible for operating medical balloon machines and for 100% inspection of each medical balloon produced. Understand the need to deliver quality product and demonstrate a commitment to quality. Contribute to continuous improvement and Lean initiatives. Follow controlled environment protocols for hygiene and gowning. Maintain regular attendance. Operate medical balloon machines with simple process / materials such as PET, Nylon, and Urethane | 7/13/2019 |
| 14719 | Nordson Salam, NH Production Associate I (Shipping) First Shift Temp to Hire HS Diploma/GED Exp: 0 years |
Position consists of manufacturing of medical components in a clean room environment while under general supervision in accordance with specifications and written procedures. This position may include machine operation, manual production using hand tools, visual inspection, physical measurements, and packaging of finished product. This position requires the ability to work with small and delicate components using a high degree of dexterity and accuracy. This position requires direct contact with medical grade components. | 7/13/2019 |
| 14720 | Nordson Salam, NH Production Associate (Shipping) Third Shift HS Diploma/GED Exp: 0 years |
Position consists of manufacturing of medical components in a clean room environment while under general supervision in accordance with specifications and written procedures. This position may include machine operation, manual production using hand tools, visual inspection, physical measurements, and packaging of finished product. This position requires the ability to work with small and delicate components using a high degree of dexterity and accuracy. | 7/13/2019 |
| 14721 | Nordson Duluth, GA Design Engineer BS in mechanical engineering Exp: 0-3 years as design engineer |
Evaluates mechanical and electromechanical systems and products by designing, applying principles of mechanics, thermodynamics, hydraulics, heat transfer, and materials. Develop mechanical and electromechanical products by studying customer requirements. Design custom equipment based on standard products. Identifies, analyzes and resolves a range of complex problem types. | 7/13/2019 |
| 14722 | Nordson Amherst, OH Test Engineer (Electrical) BS in electrical/computer engineering Exp: 0-2 years |
Electrical and mechanical aptitude with the ability to design, fabricate and wire electrical control panels and test fixtures. Troubleshoot and repair circuit boards and electronic assemblies to the component level. Write comprehensive documentation on tester hardware and software designs. Develop work instructions for system users. Provide troubleshooting support to engineering and assembly teams on products and processes | 7/13/2019 |
| 14723 | Nortech Mankato, MN Manufacturing Technician AA/AS Exp: 6 months to 1 year |
Performs machining duties and operations to include all set-ups and calculations to complete jobs independently and to meet prescribed specifications and requirements. | 7/13/2019 |
| 14724 | Nortech Mankato, MN Quality Technician - Mankato AA/AS Exp: 6 months to 1 year |
coordinates the development and implementation of the quality system, researching, developing and implementing process improvements necessary to eliminate waste and reduce inventory. Responsible for development of the performance metric system used to report on continous process improvements. | 7/13/2019 |
| 14725 | Nortech Mankato, MN Quality Engineer - Mankato BS/BA Exp: 1-2 years of experience/training |
As a quality engineer you will: Assure optimum quality in manufactured products in accordance with Company standards and contract requirements. | 7/13/2019 |
| 14726 | Norwich Pharma Norwich , NY MDAS Research Associate MS in chemistry or related Exp: 1+ year in pharma development/QC lab |
The Method Development and Analytical Services (MDAS) Research Associate is an experienced resource in performing sample testing and validating the methods necessary to support development and commercialization of pharmaceutical products. The MDAS Research Associate is responsible for performing the bench chemistry testing of pharmaceutical products supporting development of new products, incoming transfer of existing products, and analytical support of product life cycle management. The MDAS Research Associate will assist in performing method development, transfer, validation, and/or verification for methods related to analyzing raw materials, semi-finished/finished products, and stability. Customer communication and active participation as the analytical chemistry expert on work teams may be required. | 7/13/2019 |
| 14727 | Nova Biomedical Waltham, MA Chemical Filling Operator HS Diploma/GED Exp: 0-2 years as machine operator |
The Chemical Filling Operator ( Second Shift) is responsible for the proper filling, sealing and labeling of various reagents. Responsibilities: Monitoring and maintenance of the filling equipment during operation, recording necessary data into procedures, inspection of product, loading/unloading product from equipment and movement of materials. | 7/13/2019 |
| 14728 | Nova Biomedical Waltham, MA Formulation Operator HS Diploma/GED Exp: 0-2 years as compounder/formulator |
The Formulation Operator will work on our First Shift and perform batch processing of various calibrators, controls, and additional reagents required to support company produced and OEM analyzers. Essential Responsibilities: formulation of various solutions including staging of tanks, weighing and mixing of chemicals per assembly procedures (AP's) and final batch adjustment and transfer of solutions. Perform incoming inspection of raw chemicals upon receipt, maintenance of formulation equipment and cleaning as needed. Ability to accurately document and complete records of batch formulations. | 7/13/2019 |
| 14729 | Nostrum Ann Arbor, MI Packaging Technician HS Diploma Exp: 1 year in pharma/food/manufacturing |
The Packaging Technician performs routine packaging operations for the production of pharmaceutical products; operates packaging line equipment according to established SOPs and department procedures. Prepares and cleans room, equipment, facility and documents for manufacturing and packaging process. Verifies calculations, process steps and yield. Ensures that processes, tools, products and materials meet established quality standards and requirements | 7/13/2019 |
| 14730 | Neurona Therapeutics South San Francisco, CA Research Associate (Discovery Biology) MS in cell/molecular biology Exp: 0-2 years |
Responsibilities as a research associate include; Maintain human pluripotent stem cells and differentiated cells. Perform stem cell differentiation into neuronal lineages using a large variety of formats, from 384 well plates to regular and large scale culture vessels. Develop screening cell based assays using automated liquid handler for stem cell differentiation optimization. Utilize High Content Screening (HCS) technology for high-throughput analysis of cell populations. Characterize differentiated cells using a panel molecular biology methods (immuno cyto-chemistry, Flow cytometry, RT-QPCR). | 7/13/2019 |
| 14731 | NAMSA Irvine, CA Microbiology Technologist, Quality Control BS/BA Exp: 0-2 years |
Principle duties/responsibilities include: May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. | 7/12/2019 |
| 14732 | NAMSA Northwood, OH Chemist MS in chemistry or related Exp: 1 or more year lab experience |
May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. Can conduct routine testing per NAMSA SOPs for as well feasibility, one-off protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP. Conduct the study according to written instructions. Prepare and maintain the reagents required for testing. | 7/12/2019 |
| 14733 | NAMSA Brooklyn Park, MN Animal Care Technician HS Diploma Exp: 0-2 y ears |
Primarily involved in the welfare and husbandry activities of animals, including sanitation of equipment and the vivarium. Receives, identifies, and acclimates laboratory animals. Follows the Quality Manual, all NAMSA SOPs, and Process documents. Documents all required tasks. May administer treatments as directed by staff veterinarian. | 7/12/2019 |
| 14734 | NantKwest San Diego, CA Research Associate (Cell Culture Technician) BS in biology, biochemistry, immunology, or related Exp: 1-3 years cell culturing |
The Research Associate (Cell Culture Technician) will assist scientist/senior research associate for the culturing, plating, distribution, maintenance, and banking of cell culture lines. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in an efficient, highly interactive, goal-oriented team environment, and working with minimal supervision. As a team member of the cell culture group you will work to support cell and tissue culture activities. The laboratory skills and training include expertise in mammalian cell culture, aseptic technique, sterile media preparation, tissue culture room maintenance, routine testing for endotoxin and mycoplasma. | 7/12/2019 |
| 14735 | NantKwest San Diego, CA Lab Assistant BS/BA in microbiology, biology, biochemsitry, or related Exp: 1 or more year in cell culture |
The Lab Assistant is responsible for providing support throughout the facility by collecting, washing, sterilizing, and stocking laboratory glassware and consumable supplies. Also, be responsible for supporting the laboratory operations of the organization i.e., in shipping and receiving, ordering/installing of Liquid nitrogen tank. Lab assistant also has the possibility to provide assistant bench prep work based on the research demands of the department. All bench prep work is S.O.P. based and held to a high standard. As a team member of the Process Development Group you will work to support process development activities. | 7/12/2019 |
| 14736 | NantKwest Woburn, MA Research Associate MS in cell biology or immunology Exp: 1 or more year in biotech |
The successful candidate will work as part of the innovation team of NantKwest to develop next generation products for adoptive cell therapy based on the allogeneic Natural Killer (NK) platform NK-92 . Perform research and associated laboratory tasks for projects and products. Work with other scientists to design and conduct experiments on a daily basis. Design and execute experiments with minimal guidance and supervision | 7/12/2019 |
| 14737 | Natera San Carlos, CA Associate QC Operations Trainer BS/BA in biological sciences Exp: 1+ industry experience |
The Associate QC Operation Trainer supports the operation training team through various tasks and responsibilities, while becoming proficient in various laboratory assays. Maintains an active list of every lab personnel’s current department and training logs ensuring all employees are properly and consistently trained and competent. Initiates initial training of new processes, document revisions, and products. Initiates the Read and Understood workflow of our quality documents through Veeva Vault, Confluence and our Learning Management System (LMS), and any other learning management system. Assists in providing training documentations/records as needed during audits. etc. | 7/12/2019 |
| 14738 | Natera San Carlos, CA Research Technician BS/BA in biological sciences Exp: 1-2 years lab experience |
The Research Technician performs routine laboratory research and development services. Works with a multidisciplinary team. Under nominal direction, performs a variety of basic and general laboratory research and sample management tasks determined by the field and scope of the research project. | 7/12/2019 |
| 14739 | Natera San Carlos, CA Clinical Trial Assistant (CTA) HS Diploma/GED Exp: 1+ in biotech/pharma |
The Clinical Trial Assistant (CTA) will assist with the coordination of research studies, including maintaining Trial Master Files, tracking specimen procurement, tracking participant data and other study duties and organization. Maintain project and study-related documents including informed consent forms, clinical trial outlines, monitoring plans, synopses, IRB study protocols, and amendments, and clinical summaries, as required Follow protocol and assist with & coordinate training of study personnel on protocol and study manuals with external research sites | 7/12/2019 |
| 14740 | Natera San Carlos, CA Clinical Lab Scientist I BS/BA in medical technology, biological sciences or related Exp: 1-2 years as medical technologist |
Analyzes specimens and maintains equipment in good operating condition. Verify the proper specimen being analyzed and perform tests that need to be completed. Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Follows GLP (good laboratory practice): maintain clean and organized work space. etc. | 7/12/2019 |
| 14741 | Natera San Carlos, CA Clinical Data Operator I HS Diploma Exp: 0-1 years industry experience |
This position accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning. Accession samples with high accuracy and efficiency. Accurately enter patient data into the Laboratory Inventory Management System (LIMS). Scan test requisition forms and attached paperwork. Ensure that all paperwork belong to patient and upload to case. | 7/12/2019 |
| 14742 | Natera San Carlos, CA Production Engineer - Statistics/Data Analysis BS/BA in engineering, math or similar Exp: 0-2 years related |
Production Engineer - Statistics performs basic data analysis to manage daily operations for the product and its algorithms. Manage daily operations for the product algorithms. Track issues, coordinate new feature releases, and provide data analysis support to laboratory operations. Interface effectively with cross-functional teams within the company, including lab operations and software engineering. Be the "go to" person for data and algorithms issues. Track ongoing product performance metrics and investigate any variations, in cooperation with lab operations. | 7/12/2019 |
| 14743 | NatureWorks Blair, NE Production Technician HS Diploma Exp: 1-2 years manufacturing experience |
This position will work closely with other team members and be responsible for personal and plant safety, environmental compliance, commitment to continuous improvement in the quality of our product, cost control efforts and efficient operations of the plant | 7/12/2019 |
| 14744 | NATUS Middleton, WI Production Technician I AS/AA in related field Exp: 6 months in electronic circuitry repair |
Perform transactions on corporate computer inventory control system and customer relations database based on requirements of the position. Provide important data to management for regular reports. Prepare tested assemblies for customer. Develop and/or design test processes/procedures based on product specifications. Proactively problem solves departmental related issues independently and mentors other technicians in this process | 7/12/2019 |
| 14745 | NATUS Middleton, WI Quality Technician (Medical Device) AA from 2 year college or technical school Exp: 6 months + related experience |
The Quality Technician is a critical team member to handle Device History Records (DHR) Release, calibration activities, and inspection of sterile products. Ensure Device History Records (DHR) comply with requirements per the current Good Manufacturing Practices (GMP’s), which includes filing and retrieving DHR’s. Responsible for oversight of the calibration and preventive maintenance program, including, scheduling outside calibration house activities, coordinating with internal subject matter experts and monitoring calibration certificates. Implement, coordinate and assist with other projects as assigned including team participation. | 7/12/2019 |
| 14746 | NATUS Middleton, WI Repair Technician II AA in relevant field Exp: 6 months in electronic circuitry repair |
Responsiblities include: Test and calibrate assemblies to meet quality standards as well as perform electronic calibration and verify fixtures. Trouble shoot assemblies independently with exceptional computer skills. Maintain a strong commitment to high quality work with less than 2% failure rate on repairs. Maintain a 10 business day repair turnaround time on customer owned properties. Maintain minimum stock with refurbished parts to assure same day order fulfillment to assure best in class customer satisfaction | 7/12/2019 |
| 14747 | NATUS Middleton, WI Part-time Peloton Newborn Screener HS Diploma/GED Exp: 3-6 months training/experience |
In this part-time position you will work on-site at one or more hospital locations and be trained to screen newborns for common medical disorders that may occur in or after the newborn phase. In addition to performing the newborn screening tests, you will also work alongside and interact with nurses, doctors and other members of the Birth Center team at the hospital to ensure that each family has a wonderful experience during this special time in their lives. | 7/12/2019 |
| 14748 | Nelson Labs Ontario, CA Lab Analyst - M-F Day Shift BS/BA Exp: 0-2 years |
The Laboratory Analyst conducts testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. | 7/12/2019 |
| 14749 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in biology, biochemistry or related Exp: 0-2 years in biotech/pharma |
The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. | 7/12/2019 |
| 14750 | Nanostring Seattle, WA Manufacturing Research Associate I BS/BA in sciences Exp: 0-2 years in lab |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 7/12/2019 |
| 14751 | Nanostring Boston, MA Entry Level Field Service Engineer BS in mechanical/electrical/biomedial engineering Exp: Entry Level |
The Field Service Engineer performs field installations, service, and preventative maintenance on the NanoString instrument portfolio. Install instrumentation in both research and medical diagnostic laboratories in accordance with IQ/OQ/PQ procedures. Perform annual preventative maintenance procedures on systems installed at customer sites. Document all activities and update/maintain instrument configuration databases in compliance with all Quality Assurance procedures | 7/12/2019 |
| 14752 | Nelson Labs Salt Lake City, UT Validation Specialist BS/BA Exp: 1 or more years applicable experience |
Responsible for preparing, executing and finalizing test method validations, equipment, system and utility IQ, OQ and PQs as well as maintain control charts. Also, required to maintain the re-qualification schedule per the current validation master plan schedule. | 7/12/2019 |
| 14753 | Nelson Labs Salt Lake City, UT Lab Analyst BS/BA, AS/AA or HS Diploma Exp: 0-2 years |
The Laboratory Analyst conducts testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. | 7/12/2019 |
| 14754 | Semma Therapeutics Cambridge, MA (Sr.) Research Associate (Scientist) – Cell Biologist R&D (MA) MS in molecular or cell biology or related Exp: 1-2 years |
Semma Therapeutics, a biotechnology company focused on developing a pluripotent stem cell-based cell therapy for Type 1 diabetes, is seeking an outstanding research associate to join its growing team. The full-time role will focus on tissue culture, molecular and cellular characterization, process and assay developments. Under the supervision of a Principal Scientist and working closely within the Cell Biology department on novel R&D programs, the associate will be responsible for the day-to-day execution of specific projects. The position will be located in Cambridge/Boston, MA. Responsibilities: Culture and differentiation of human pluripotent stem cells in various conditions, including differentiation protocol optimization. Co-design and help execute well-controlled in vitro experiments to demonstrate technological feasibility and improvements for characterization of cell product and/or achieve proof-of-concept. etc. | 7/9/2019 |
| 14755 | Senseonics Germantown, MD Staff Accountant BS/BA in accounting or equivalent Exp: 1-3 years |
We are looking for a full-time Staff Accountant to support the finance team with all aspects of the day to day accounting function as needed. The ideal candidate is ready to work hard, have fun, and utilize their technical skills to further develop their accounting career. This is an excellent opportunity where you will gain valuable experience and have impact in multiple facets of operational accounting and related tasks in a publicly traded, dynamic, rapidly growing business. Qualifications: Record accounting transactions following Senseonics internal control processes. Perform account reconciliations and close procedures. Support the preparation and analysis of monthly and quarterly results. etc. | 7/9/2019 |
| 14756 | SeraCare Gaithersburg, MD Research Associate II MS in biochemistry, molecular biology, or related Exp: Recent graduates |
Advance SeraCare’s purpose of understanding disease by supporting the research and development of new precision diagnostic products. Support includes independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material. RESPONSIBILITIES: Perform general molecular techniques such as nucleic acid purification, gel-electrophoresis, RNA transcription, cell culture, and bacterial culture. Perform nucleic acid analysis (RNA/DNA integrity analysis, real time qPCR, digital PCR) and analyze results. etc. | 7/9/2019 |
| 14757 | Sigilon Therapeutics unspecified, Assistant/Associate Scientist, Biomaterials BS/MS in biochemistry, biology, engineering, or related Exp: 0-2 years |
Responsibilities: Encapsulation of cells in novel biopolymer systems. Maintenance and setting up of biopolymer device encapsulation systems. Establishing protocols and SOPs for encapsulation procedure. Work in a matrixed environment to ensure biomaterials meet the needs of the in vivo and cell biology teams. With increasing independence, plan, design and execute of a series of experiments that provide the research findings necessary for the completion of an assigned project. Demonstrate understanding and application of relevant scientific literature to the design of experimental protocols. etc. | 7/9/2019 |
| 14758 | Sigvaris Group Peachtree City, GA Technician AS or equivalent certification Exp: 1-3 years |
This position is responsible for the general repair of hosiery knitting machines to ensure first quality products are produced to company specifications. Performs required/needed maintenance knitting machines to ensure machines are operating in good working order. Addresses machine stops to keep machines operating efficiently. Performs preventative maintenance as outlined in weekly PM sheets. Follows proper procedures to ensure product is knit to specifications. Sets up and sizes different styles/series on machines and ensures proper sizing to spec before released to production. etc. | 7/9/2019 |
| 14759 | Smith & Nephew Memphis, TN Quality Engineer I (Medical Device-Hips) BS in mechanical, manufacturing, electrical, or industrial engineering Exp: 0-2 years |
Reporting into the Quality Department, this role has responsibility for Quality related actions in support of New Product Development (NPD, Design Quality). Works collaboratively with project team members to develop and manage project plans. Champion design control and risk management activities for assigned projects. Evaluate risk and verification implications for purposed post launch design changes. Continuously improve Design Control procedures and maintain procedural compliance. Supports new product development and implementation of new products via development of an overall quality plan, including needed inspection, test, and audit procedures; identification of needed reliability testing; identification, procurement, and maintenance of needed engineering test equipment; and support of process/product validation. Responsible for development and release of engineering design documentation. etc. | 7/9/2019 |
| 14760 | Semma Therapeutics unspecified, MA GMP Manufacturing Associate, Clinical Materials (MA) BS/MS in biological or chemical engineering, process sciences, or related. Exp: 6+ months |
Semma Therapeutics is a biotechnology company pioneering the development of a stem cell-based cure for diabetes. We are seeking an outstanding manufacturing associate for clinical materials to join our growing team. This full-time role reports to the Director of Manufacturing, and will be responsible for the technology transfer and production of cell therapy products to support Semma’s Phase I/II clinical trials. Clinical materials produced in the facility will be manufactured according to Good Manufacturing Practices (GMP) and conducted under Investigational New Drug (IND) applications with the US Food and Drug Administration (FDA). etc. | 7/9/2019 |
| 14761 | Sinclair Research Auxvasse, MO Animal Technician HS Diploma/GED Exp: Entry level |
The ideal candidate will be hard-working and ready to be hands on. In this role, you will have a chance to participate daily in our research by working closely with our study directors, senior technicians, and scientists in order to conduct studies. Animal Technicians begin by learning the basics of data collection and animal husbandry and have the chance to move up into high level Technician roles. This is an entry level position and a great place to start your career in research and see where you may end up! Many of our Animal Technicians become Research Technicians, Laboratory Technicians or even Scientists as they continue to train and grow here at Sinclair. | 7/9/2019 |
| 14762 | Sinclair Research Auxvasse, MO Animal Caretaker HS Diploma/GED Exp: Entry level |
The ideal candidate will have a passion for animal welfare and a great work ethic. Hard-working individuals looking for a great environment and a chance to make a difference will fit right in. Your primary role will be taking care of our animals and sanitizing their housing and our buildings. This may include caring for rats, mice, rabbits, dogs, cats, swine, or even cattle! There may be some heavy lifting and some dirty work involved but, if you love the idea of spending your day with animals, it's worth it to take care of our little heroes. | 7/9/2019 |
| 14763 | Siemans Munhall, PA Systems Engineer 2 - Rail Automation BS in electrical engineering, computer science, or related Exp: 1-2 years |
In this Systems Engineer role, you will support moderate to complex systems engineering projects, obtain requirements, and develop new requirements based on customer needs. You will also translate requirements into detailed systems/product specifications and participate in systems analysis as well as systems/product validation and verification. You will provide technical support to systems/product users and other partners, providing resolution to engineering problems (HW, SW, Test) and implements system improvements and reports on the effectiveness of existing and new systems/products. Responsibilities: Participate in rotational exposure to all aspects of R&D life cycle to understand products; customer requirements and interface of hardware/software and system integration. Prepares test and diagnostic programs, designs test fixtures and equipment, and completes specifications and procedures for new products under direct supervision. etc. | 7/9/2019 |
| 14764 | Siemans Louisville, KY Systems Engineer 2 - Rail Automation BS in electrical engineering, computer science, or related Exp: 1-2 years |
In this Systems Engineer role, you will support moderate to complex systems engineering projects, obtain requirements, and develop new requirements based on customer needs. You will also translate requirements into detailed systems/product specifications and participate in systems analysis as well as systems/product validation and verification. You will provide technical support to systems/product users and other partners, providing resolution to engineering problems (HW, SW, Test) and implements system improvements and reports on the effectiveness of existing and new systems/products. Responsibilities: Participate in rotational exposure to all aspects of R&D life cycle to understand products; customer requirements and interface of hardware/software and system integration. Prepares test and diagnostic programs, designs test fixtures and equipment, and completes specifications and procedures for new products under direct supervision. etc. | 7/9/2019 |
| 14765 | Siemans Norcross, GA Fire Alarm Commissioning Technician HS diploma Exp: 1-3 years |
The ideal candidate will be someone with an exceptionally strong fire alarm system background and be able to fulfill all the required duties of a Fire Alarm Installation Technician. Responsibilities: This candidate must possess strong written and verbal communication skills, have exceptional computer skills, and have a strong sense of self reliance. Must possess the ability to install, program and troubleshoot complex networked fire alarm/mass notification systems with limited or no supervision. May require some overtime hours at night, on weekends and at a moment’s notice for emergency calls. Exceptional work ethic and attention to detail. | 7/9/2019 |
| 14766 | Siemans Louisville, KY System Engineer 1 - Rail Automation BS in electrical engineering, computer science, or related Exp: 1-2 years |
In this Systems Engineer role, you will provide systems engineering support on moderate to complex systems engineering projects and participate in requirements capture; develops new requirements based on customer need. You will also translate requirements into detailed systems/product specifications. In addition, you will participate in systems analysis, systems/product validation and verification and provide technical support to systems/product users and other stakeholders, providing resolution to engineering problems (HW, SW, Test). You will also implement system enhancements and report on the effectiveness of existing and new systems/products. etc. | 7/9/2019 |
| 14767 | Siemans Rural Hall, NC CNC Milling Operator HS diploma or AAS in machining technology Exp: Entry level |
We're looking for dedicated people wit the skills and vision to build a better tomorrow. Join our team as an Operator and you will use micrometers and other measuring tools to repair large, 500 pounds to 10 tons, rotating equipment. The majority of your work is lathe work for shaft repair. You will also do mill work to make specialty items necessary for the repairs. All your work is performed to tight tolerances. The primary purpose of this position is to operate a variety of machine tools according to manufacturing and engineering specifications and/or set-up less complex (i.e. saws, straddle mills etc.) machine tools. etc. | 7/9/2019 |
| 14768 | Siemans East Walpole, MA Data Scientist BA/BS Exp: Entry level |
At Siemens Healthineers, we are passionate about enabling healthcare professionals to deliver high quality patient care, and to do so affordably. A leading global healthcare company, Siemens Healthineers continues to strengthen our portfolio of medical imaging and laboratory diagnostics, while adding new offerings such as managed services, consulting, and healthcare IT services – as well as further technologies in the growing market for therapeutic and molecular diagnostics. Siemens Healthineers develops innovations that support better patient outcomes with greater efficiencies, giving providers the confidence they need to meet the clinical, operational and financial challenges of a changing healthcare landscape. etc. | 7/9/2019 |
| 14769 | Siemans Newark, DE Pharmaceutical Tech 2-Production AS in biology, chemistry, biochemistry or related Exp: Entry level |
Now’s our time to inspire the future of healthcare together. Join our team now at Siemens Healthineers as Pharmaceutical Tech 2. This is a role well suited to an ambitious professional, looking for the next step in their career. As a Pharmaceutical Tech 2 – in production, you will be responsible for: Formulating and testing reagents and calibrators by following production worksheets and area procedures. Drug Enforcement Agency (DEA) background check clearance is required. etc. Responsibilities: Formulates and test reagents and calibrators for Atellica, Syva, Advia, Immulite and OEM product lines. Follows area procedures and manufacturing work instructions. etc. | 7/9/2019 |
| 14770 | Sekisui Xenotech Kansas City, KS Research Assistant BS in biological or chemical sciences Exp: 1+ years |
Sekisui XenoTech, LLC is currently hiring for a Research Assistant for our Enzyme Incubations Team within the Program Execution department. The Research Assistant assists with routine laboratory functions including diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintains inventory of supplies, and various other responsibilities. Essential duties and responsibilities include, but are not limited, to the following: Design and conduct routine and atypical experiments. Maintains laboratories and equipment and performs minor repairs on equipment, with supervision. Maintains appropriate logs, records and study notebooks. Processes and reviews data. Adheres to Good Laboratory Practice regulations and Sekisui XenoTech safety policies and procedures. Sekisui XenoTech, LLC is currently hiring for a Research Assistant for our Enzyme Incubations Team within the Program Execution department. The Research Assistant assists with routine laboratory functions including diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintains inventory of supplies, and various other responsibilities. Essential duties and responsibilities include, but are not limited, to the following: Design and conduct routine and atypical experiments. Maintains laboratories and equipment and performs minor repairs on equipment, with supervision. Maintains appropriate logs, records and study notebooks. Processes and reviews data. Adheres to Good Laboratory Practice regulations and Sekisui XenoTech safety policies and procedures. | 7/9/2019 |
| 14771 | Sekisui Xenotech Kansas City, KS Scientist II BS/MS in biological or chemical field Exp: 1+ years |
Sekisui XenoTech, LLC is currently looking for a Scientist II or higher in our Program Oversight department. This department is responsible for overseeing study protocols for disciplines such as enzyme inhibition, enzyme induction, drug metabolism, drug transport, etc. Scientists are responsible for ensuring that contract research studies are performed according to protocol, facility SOP and the appropriate regulations. Essential duties and responsibilities include, but are not limited, to the following: Review and interpret data. Respond to Quality Assurance audit reports. Participate in the training of other scientists. Write Standard Operating Procedures. Troubleshooting technical problems. Coordinates the conduct of in vitro metabolism or transport assays. Prepares, or assists in the preparation of reports requiring specialized scientific knowledge. Interacts with clients during site visits, QA audits, and other study related issues. Clearly communicates results to Sponsors. Sekisui XenoTech, LLC is currently looking for a Scientist II or higher in our Program Oversight department. This department is responsible for overseeing study protocols for disciplines such as enzyme inhibition, enzyme induction, drug metabolism, drug transport, etc. Scientists are responsible for ensuring that contract research studies are performed according to protocol, facility SOP and the appropriate regulations. Essential duties and responsibilities include, but are not limited, to the following: Review and interpret data. Respond to Quality Assurance audit reports. Participate in the training of other scientists. Write Standard Operating Procedures. Troubleshooting technical problems. Coordinates the conduct of in vitro metabolism or transport assays. Prepares, or assists in the preparation of reports requiring specialized scientific knowledge. Interacts with clients during site visits, QA audits, and other study related issues. Clearly communicates results to Sponsors. | 7/9/2019 |
| 14772 | Selecta Biosciences Watertown, MA Research Associate I/II, Biology BS/MS in biology, biotechnology, pharmaceuticals, or relavent Exp: 0-3 years (BS), 0-2 years (MS) |
The Research Associate's primary role is to conduct in vivo and in vitro studies to advance Selecta's drug discovery programs. Position participates in designing and executing experiments aimed at evaluating the efficacy of Selecta's nanoparticles in relevant disease models and understanding the mechanism of action of drug candidates. The position is approximately 80% lab and 20% non-lab work. Primary Duties and Responsibilities: Plan the scheduling and designing of experiments to evaluate the efficacy of nanoparticles and understanding the mechanism of action of drug candidates. Participate and sometimes take a lead role in executing animal experiments including injections and processing tissue and serum samples. etc. | 7/9/2019 |
| 14773 | Selecta Biosciences Watertown, MA Research Associate I/II, Quality Control BS/MS in chemistry or related Exp: 1-3 years |
Selecta Biosciences is seeking a talented, dedicated, and enthusiastic Research Associate to join our Quality Control group! The Research Associate is responsible for producing timely and accurate data for analyses targeting a variety of nanoparticle components such as small molecules, peptides, proteins, oligosaccharides and synthetic polymeric material in support of the development of preclinical and clinical products based on the company's proprietary synthetic nanoparticle technology developed to elicit the desired and optimal immune response. Principal Duties/Responsibilities: Executes routine R&D and release and stability GMP testing for API, bulk drug substance and final drug product intended for clinical supply and provides timely and accurate data generation using a variety of assays including HPLC techniques and plate-based methods. etc. | 7/9/2019 |
| 14774 | Singota Solutions Bloomington, IN SCM Associate Operator HS Diploma Exp: 0-1 years |
Obtain training on different aspects of logistics and apply them consistently and efficientlyto operations hired to perform: Pulling material from warehouse using Fork truck and scissor lift when necessary. Shipping of daily client material on designated truck. Shipping of client material via FedEx, UPS, etc. Accepting client material from delivery drivers and inspecting for damage. Working to keep any client material put in appropriate bin locations when necessary to keep staging areas clear. Participate in collaborating or writing of deviations, investigations, and CAPAs to continuously improve operations. Demonstrate good documentation practices. etc. | 7/9/2019 |
| 14775 | Scantibodies Laboratory Santee, CA Customer Service Representative II (Bilingual in Mandarin) College degree preferred Exp: 1-2 years customer service experience |
Essential Duties: Receive and respond to correspondence and phone calls from customers, including entering customer orders, researching information and tracking progress of orders. Be responsible for customer service to a variable number of directly assigned customers and be prepared to assume representation for additional customers, both as new assignments and “unassigned” customers. Be familiar with the top 10-20 products and top 30-50 customers of SLI. Be familiar with the product lines of the various production departments within SLI (i.e., who makes which products for order processing and technical support questions.) Receive, review and enter into record customer specifications, assuring proper review and approval by production, QA and other appropriate personnel. etc. | 7/8/2019 |
| 14776 | Sciecure Pharma Monmouth, NJ QC Document Review BS in chemistry or related Exp: 1-2 years in GMP lab |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. Responsibilities: Review of documentation generated during method validation, method verification, stability testing, routine testing and other analyses. Review documentation, results and reports from raw material and finished product analysis for accuracy and completeness. Provide feedback from reviews to analysts and supervisor and ensure necessary action are taken to correct or prevent error. Review data using a systematic approach to ensure compliance with procedures and specifications. Review and audit projects as required. Perform other duties assigned by supervisor as needed. etc. | 7/8/2019 |
| 14777 | Sciecure Pharma Monmouth, NJ ARD Intern BS/MS in chemistry, biology or related Exp: Recently graduated |
The Analytical R&D laboratory supports development and validation of methods. All activities are performed in accordance with specifications, SOPs, and regulatory requirements. This position does not require working experience; however, previous lab experiences are preferred. Full-time position at Sciecure Pharma will be considered by the end of internship. Responsibilities: Analyze data, document results, maintain laboratory notebook per cGMP and internal guidelines. Communicate results in written and oral presentations. Contribute to continuous improvement within the group. Comply with FDA, performing all work in a safe manner. Maintain proper records in accordance with all SOP's and policies. Provides support for ordering and maintaining inventory of laboratory materials and equipment. Performs other miscellaneous duties as required. etc. | 7/8/2019 |
| 14778 | SDIX Windham, ME Animal Technician I HS diploma/AS Exp: Entry level |
This position participates in a team of technicians responsible for animal husbandry and antibody production activities. All job responsibilities to be conducted within standard operating procedures and regulatory compliance. Responsibilities and Duties: Clean and disinfect cages, rooms and support areas. Feed animals; maintain water systems, ventilation settings, pest control, and related tasks. Conduct animal identification, animal breeding programs and related tasks. Conduct animal health monitoring and documentation. etc. This position participates in a team of technicians responsible for animal husbandry and antibody production activities. All job responsibilities to be conducted within standard operating procedures and regulatory compliance. Responsibilities and Duties: Clean and disinfect cages, rooms and support areas. Feed animals; maintain water systems, ventilation settings, pest control, and related tasks. Conduct animal identification, animal breeding programs and related tasks. Conduct animal health monitoring and documentation. etc. This position participates in a team of technicians responsible for animal husbandry and antibody production activities. All job responsibilities to be conducted within standard operating procedures and regulatory compliance. Responsibilities and Duties: Clean and disinfect cages, rooms and support areas. Feed animals; maintain water systems, ventilation settings, pest control, and related tasks. Conduct animal identification, animal breeding programs and related tasks. Conduct animal health monitoring and documentation. etc. | 7/8/2019 |
| 14779 | Seattle Genetics Bothell, WA GMP Support Specialist I University degree Exp: 0-2 years in a regulated environment |
This position supports Facilities GxP (GMP & GLP) compliance by acting as a liaison between Facilities, QC, GLP and QA. This position is responsible for supporting Facilities related incident investigations, CAPA, CAPA effectiveness, audits and other Quality System activities. This position supports the Master Equipment File (MEF) system by providing oversight of the document filing system. This position helps maintain departmental training compliance by providing administrative support. This position may help support validation by assisting with periodic reviews and other qualification activities. Drafts Facilities SOPs and work practices. | 7/8/2019 |
| 14780 | Seattle Genetics Bothell, WA Research Associate I/II, Formulation and Drug Product Sciences BS in biochemistry, engineering, chemistry, biological sciences, or related Exp: 0-2 years |
The Formulation and Drug Product Sciences Group at Seattle Genetics is seeking a highly motivated Research Associate to assist in the formulation development for therapeutic antibodies and antibody-drug conjugates. The ideal candidate should have a background in biochemistry or related discipline with previous laboratory experience, strong critical thinking skills, good interpersonal skills, and is self-motivated. Responsibilities: Conduct experiments and analyze results leading to development of robust formulations for antibodies and antibody drug conjugates. Generate and interpret high quality data. Perform study and instrument troubleshooting. Author technical reports. Summarize and present results in group and team meetings, contribute to discussions | 7/8/2019 |
| 14781 | Seattle Genetics Bothell, WA Research Associate II, Process Chemistry MS in chemistry Exp: 0-5 years |
The successful candidate will be responsible for developing novel synthetic routes and chemical processes for anti-cancer drugs and proprietary drug linkers used for antibody conjugation. The ideal candidate should possess an in-depth knowledge of organic chemistry, reaction mechanisms, and familiarity with modern synthetic methods and analytical techniques. Candidates will have demonstrated creativity and independence in solving synthetic problems and ultimately developing robust chemical processes which he or she will work to transfer to CMO’s. Experience and expertise in peptide synthesis is desirable. Responsibilities: Conduct route scouting studies to establish novel synthetic routes for drug linkers and active pharmaceutical agents. Design and execute experiments which define parameters for robust and efficient chemical processes. etc. | 7/8/2019 |
| 14782 | Seattle Genetics Bothell, WA Research Associate I/II, Target Validation BS in cell biology, biochemistry, biomedical engineering, or related Exp: 0-2 years |
The Target Validation group is seeking an energetic and highly motivated Research Associate to augment our efforts to identify and characterize molecular targets for our industry-leading ADC technology. The successful candidate will design, conduct, and interpret experiments utilizing a diverse array of techniques aimed at discovery and validation of early targets in Seattle Genetic’s drug discovery pipeline. Responsibilities: Standard target validation methodologies will include flow cytometry, in vitro cytotoxicity assays, immunohistochemistry, Western blotting, and a variety of biochemical and cell-based assays. etc. | 7/8/2019 |
| 14783 | Sebela Pharma unspecified, QC Chemist BS in chemistry or related Exp: 0-2 years in a cGMP environment |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. PRINCIPAL DUTIES AND RESPONSIBILITIES: Perform testing of raw materials and products. Perform instrument qualification and maintenance. Perform test method validation/verification. Review analytical data for completeness, accuracy, and compliance. Perform training on procedures, equipment, or quality systems. Other duties as assigned. Individual contributor, but may be assigned as a project lead or trainer commensurate with experience or expertise. etc. | 7/8/2019 |
| 14784 | Sedia Biosciences Portland, OR QC Technician HS diploma/AS Exp: 1 year |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. Demonstrates a high level of independent judgment and discretion in the timely identification, investigation and resolution of events impacting the Quality of products and processes. | 7/8/2019 |
| 14785 | Sedia Biosciences Portland, OR Manufacturing Technician HS diploma/AS Exp: 1 year |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. The Manufacturing Technician will adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance. | 7/8/2019 |
| 14786 | Sedia Biosciences Portland, OR Scientist/Associate Scientist(R&D-Product Development) MS Exp: 1-3 years |
Sedia Biosciences Corporation of Portland Oregon is seeking a motivated, responsible, and resourceful individual to work as part of our team as a Scientist or an Associate Scientist. This position would be a full-time exempt position (40 hours per week) at our primary laboratory facility in Northeast Portland. The successful candidate will be responsible for running laboratory tests, recording data, performing some degree of data analysis, drafting protocols, and communicating with managers from R&D and other departments. They will also be asked to participate in production of prototype products, and assist in transition of those procedures (through training and/or record-keeping) to our manufacturing department. Workflow is approximately 50-70% laboratory work, with the remainder being office work. The nature of our work requires the candidate to be capable of working comfortably in a BSL 2 laboratory. | 7/8/2019 |
| 14787 | Seer , CA Research Associate, Assay Development BS/MS Exp: 1-4 years |
Seer is seeking a Research Associate, Assay Development, who will implement and contribute to the design of biochemical experiments that support the development and operation of the company’s protein assays. These assays form the foundation of breakthrough products and services in proteomic data, which Seer will provide to patients and clinicians. The Research Associate, Assay Development will report to the Senior Scientist of Assay Development. The specific assays developed for Seer will leverage nanoparticles, immunoassays, as well as the use of mass spectrometry as a detection approach. The successful candidate is expected to have a background in biochemistry, biology, or pharmacology with experience in academia and/or industry, ideally within life sciences companies. Experience in industry, including the implementation of SOPs and testing in support of clinical or pre-clinical products is strongly desired. This role will be based in the South San Francisco office through late 2019. Please note, the company is moving to its permanent location in Redwood City at the end of the year. | 7/8/2019 |
| 14788 | Seer , CA Research Associate, Chemisty MS Exp: 0-2 years |
Seer is seeking a Research Associate in the chemistry group, who will be empowered to support the development of the company’s core technology platform. The ideal candidate will have significant relevant experience and a track record of accomplishments in academia or in the life sciences/pharmaceutical/biotechnology industry. This role is part of a team focused on nanoparticle synthesis, characterization, and assay development. This role requires skills including particle synthesis, surface modification, and incorporates both organic and inorganic chemistry. This role will be based in the South San Francisco office through late 2019. Please note, the company is moving to its permanent location in Redwood City at the end of the year. | 7/8/2019 |
| 14789 | Sciex Calsbad, CA Production Scientist I BS in biological sciences, chemistry or related Exp: 1-2 years |
Manufacturing of Life Science products according to standard operating procedures and work instructions. Performs simple calculations according to procedures, and maintains accurate records of work performed according to GLP, GMP, and QSMRs. Independently prioritize work assignments and consistently demonstrate the ability to perform assigned tasks in manufacturing setting. Typically receives minimal instruction on routine work; general instructions on new assignments. Maintain a high level of productivity in the laboratory setting while following Good Laboratory Practices (GLP) Maintain a safe, pleasant and efficient work environment. Collaborate with other departments in process improvement or new product launch projects. Participate in special projects and department meetings via input, feedback and execution of assigned tasks. Manufacturing of Life Science products according to standard operating procedures and work instructions. Performs simple calculations according to procedures, and maintains accurate records of work performed according to GLP, GMP, and QSMRs. Independently prioritize work assignments and consistently demonstrate the ability to perform assigned tasks in manufacturing setting. Typically receives minimal instruction on routine work; general instructions on new assignments. Maintain a high level of productivity in the laboratory setting while following Good Laboratory Practices (GLP) Maintain a safe, pleasant and efficient work environment. Collaborate with other departments in process improvement or new product launch projects. Participate in special projects and department meetings via input, feedback and execution of assigned tasks. Manufacturing of Life Science products according to standard operating procedures and work instructions. Performs simple calculations according to procedures, and maintains accurate records of work performed according to GLP, GMP, and QSMRs. Independently prioritize work assignments and consistently demonstrate the ability to perform assigned tasks in manufacturing setting. Typically receives minimal instruction on routine work; general instructions on new assignments. Maintain a high level of productivity in the laboratory setting while following Good Laboratory Practices (GLP) Maintain a safe, pleasant and efficient work environment. Collaborate with other departments in process improvement or new product launch projects. Participate in special projects and department meetings via input, feedback and | 7/8/2019 |
| 14790 | Sekisui Diagnostics San Diego, CA Research Associate BS/MS Exp: 1-2 years for BS, 0-2 for MS |
Initiates, directs and executes pre-clinical scientific research and/or development strategies in research and/or development. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems. Plans and executes laboratory research. Maintains broad knowledge of state-of-the-art principles and theories. May act as spokesperson on corporate research and development and advise top management. May participate in development of patent applications. Interfaces with various departments and serves as internal consultant. etc. | 7/8/2019 |
| 14791 | Sekisui Diagnostics San Diego, CA QC Technician II BS Exp: 0-1 year |
To perform routine QC techniques by adhering and following written procedures under general supervision. Responsibilities:· Performs raw materials, in process, final release testing, stability testing, customer complaints investigation and environmental monitoring according to a defined plan. Reviews results for accuracy and interpretation. Executes defined tasks and successfully attains completion with guidance. Collaborates with supervisor to establish a level work load. Responsible for meeting the daily and weekly testing schedule. Supports QC metrics for work center utilization, efficiency and router accuracy; responsible and accountable for accuracy and timeliness of system transactions. Understands and adheres to all QSR, ISO, Safety and Legal requirements. Performs all other tasks as required. etc. | 7/8/2019 |
| 14792 | Sekisui Diagnostics Charlottetown, PE Research Associate BS/MS Exp: 0-2 years |
The Research Associate will be responsible for designing, executing and interpreting experiments and analytical procedures under general supervision. Opens a New Window. Initiates, directs and executes pre-clinical scientific research and/or development strategies in research and/or development. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems. Plans and executes laboratory research. Maintains broad knowledge of state-of-the-art principles and theories. May participate in development of patent applications. Interfaces with various departments. Responsibilities: In consultation with supervisor or manager, designs procedural and experimental approach to meet designated scientific objectives. Initiates and develop plans to ensure the timely completion of several sets of experiments. Performs complex analytical procedures using established techniques. | 7/8/2019 |
| 14793 | Sekisui Diagnostics Charlottetown, PE Packaging Associate II HS diploma Exp: 1 year |
To work on automated and semi-automated filling and labeling equipment using vision systems as well as work on assembly lines to complete final kit assembly and perform manual labeling operation. Responsibilities: May include some or all the following: Perform labeling of products using automated labeling equipment equipped with vision systems. Gain full knowledge on minimum of 2 automated labeling equipment. Opens a New Window. Perform dispensing of products using automated dispensing equipment equipped with vision systems. Gain full knowledge on minimum of 2 automated dispensing equipment. Perform filling of bulk products using filling equipment and floor model weight scales. Perform pooling of diagnostics reagents to avoid contamination of product. Ability to complete all job-related documentation associated with minimal errors. etc. | 7/8/2019 |
| 14794 | Mirus Bio Madison , WI Shipping Associate HS Diploma/GED Exp: 1 or more years in shipping/logistics |
he Shipping Associate will pick orders from inventory and prepare them for shipping in an accurate and timely fashion. The Shipping Associate is also responsible for assembling finished goods for entry into inventory. This position will report directly to the Shipping Manager. Prepare and execute domestic and international shipping of Mirus products using FedEx, UPS, DHL and freight forwarders. Assemble finished goods for inventory. Follow departmental Standard Operating Procedures (SOPs) | 7/6/2019 |
| 14795 | Mission Pharmacal Boerne, TX Tablet Tech-Night HS Diploma/GED Exp: 1 or more years |
Operates machines, tends the tablet press, transfers products into containers, weighs, mixes materials, records documentation, and performs basic routine maintenance. Cleans equipment and rooms per SOP’s and monitors product quality. Verifies all batches by control number, part number, and quantity per specifications prior to running the lot. Starts machine and observes operation to ensure all machinery is operating properly. Stops machine and reports any malfunction to Tableting Lead. Assist in repairs. Performs set-up of tablet press, assigned preventive maintenance procedures, parts assembly, and cleaning hardware. Ensures each product is tableted according to specifications and standard operating procedures. | 7/6/2019 |
| 14796 | Moderna Norwood, MA Engineer I, Sterile Product Technology BS or MS in chemical/biomedical engineering or related Exp: BS: 0-5 years, MS: 0-2 years |
Moderna is seeking a highly skilled and motivated Engineer I/II in Sterile Product Technology, a process development team residing in Moderna’s Technical Development organization, to support mRNA lipid nanoparticle (LNP) process development that enables our clinical supply. The applicant will play a critical role helping bring medicines to patients as Moderna’s portfolio begins to shift towards late-stage development. The primary role for this position will be to support fill/finish process development and scale-up work, with eventual ownership of experimental design and execution. The applicant will collaborate closely with Technical Development, Pre-clinical and GMP Production, Quality, and Drug Product Analytical Development groups on innovative process development efforts. Applicants should have relevant pharmaceutical experience with fill/finish processes and drug product development. | 7/6/2019 |
| 14797 | Moderna Cambrdige, MA (Contract) Research Associate, Process and Nucleic Acid Innovation BS or MS in molecular biology, biochemistry, biology or related Exp: 1-3 years research experience |
This role will conduct research in the Process and Nucleic Acid Innovation group to develop and test novel nucleic acid constructs for use in various interdepartmental projects. A successful candidate will be inquisitive about the science and capable of problem solving by consulting literature and colleagues and designing experiments to test hypotheses. This role will utilize various techniques associated with RNA and DNA synthesis and purification, mammalian cell culture, and in vitro molecular biology. This assignment is expected to last 12 months. | 7/6/2019 |
| 14798 | Moderna Cambrdige, MA (Contract) Research Associate, Analytical Operations BS or MS in analytical chemistry, biochemistry, chemical engineering or related Exp: BS: 1-3 years, MS: 0-2 years |
The primary responsibilities of this role will be to support implementation of analytical methods and routine testing messenger RNA therapeutic drug substances and drug products, including both chemical separation and biophysical techniques. The incumbent will be expected to undertake laboratory work to support in-process sample testing of critical non-GMP large scale batches including IND enabling drug substance and drug product batches. The analyst will be responsible for generation and reporting of analytical results. | 7/6/2019 |
| 14799 | Moderna Norwood, MA (Contract) Manufacturing Associate I, 2nd Shift BS/BA in biology, chemistry, chemical/biomedical engineering Exp: 0-2 years |
The individual in this role will be responsible for production of DNA for all constructs using custom automation, Hamilton liquid Handlers, and chromatography solutions. The successful candidate must demonstrate the ability to quickly master new processes and the drive to be part of a dynamic, fast paced, and highly motivated team. They must have training in chromatography (UPLC/HPLC), liquid handlers, basic molecular biology techniques, and ability to work with custom automation. The anticipated time frame for this assignment is 6 months. | 7/6/2019 |
| 14800 | Moderna Norwood, MA (Contract) Manufacturing Associate I BS/BA in biology, chemistry, chemical/biomedical engineering Exp: 0-2 years |
The individual in this role will be responsible for production of DNA for all constructs using custom automation, Hamilton liquid Handlers, and chromatography solutions. The successful candidate must demonstrate the ability to quickly master new processes and the drive to be part of a dynamic, fast paced, and highly motivated team. They must have training in chromatography (UPLC/HPLC), liquid handlers, basic molecular biology techniques, and ability to work with custom automation. The anticipated time frame for this assignment is 6 months. | 7/6/2019 |
| 14801 | MICR Indianapolis, IN Medical Research Study Coordinator CCRC certification + degree Exp: 1-3 years clincal research |
Individual will be responsible for implementing clinical research protocols. | 7/6/2019 |
| 14802 | Molecualr MD Cambridge, MA Laboratory Assistant HS Diploma/GED Exp: 3 months or more work experience |
The Laboratory Assistant (Lab Assistant) is self-motivated and responsible for assisting the Technical Supervisor with clerical laboratory duties. They diligently strive to continually maintain a clean, professional, and safe working environment. Duties include specimen receiving and accessioning, storage of clinical specimens, assisting with lab cleaning/maintenance, equipment/temperature support, monitoring, lab supply inventory/receiving, clerical administrative responsibilities. | 7/6/2019 |
| 14803 | Morphic Therapeutics Waltham, MA Research Associate, Immunology BS in biology or related Exp: 1-2 years in research |
The successful candidate will join a dynamic, multi-disciplinary team of scientists, playing a key role to evaluate new immunotherapeutic strategies and drug candidates. The candidate is expected to be multi-tasking and able to execute experiments with strong attention to detail under supervision. | 7/6/2019 |
| 14804 | MP Biomedicals Santa Ana, CA Biochemicals Product Specialist MS in product management/life sciences Exp: 0-3 years |
Expand the Life Sciences business with research reagents for the fields of biochemistry, molecular biology, immunology, cell biology and neuroscience. Identify new product and market opportunities and deliver exceptional product technical support, answer questions regarding our products and present our products in the most favorable and understandable form to influence the buying decisions of our customers. Continually follow market trends and identify new sales potential through the addition of new products and application focused on select market segments. | 7/6/2019 |
| 14805 | MyoKardia South San Francisco, CA Research Associate I, Biology BS or MS in biology, biochemistry, physiology or related Exp: 0-2 years |
. The successful candidate will work both independently and collaboratively as part of the Cell Biology team. Perform a diverse range of cell-based assays to characterize lead candidates for various therapeutic mechanisms. Expand and differentiate human iPSCs towards the cardiovascular lineage. Execute a range of experiments using molecular biology and cell biology techniques including nucleic acid and protein isolation, qPCR, virus preparation, and metabolic assays. Manage aspects of housekeeping for the cell culture lab, including preparing reagents, helping with room maintenance, ordering and restocking. | 7/6/2019 |
| 14806 | Myriad Genetics Salt Lake City, UT Patient Advocate Triage I BS/BA in biology or health sciences Exp: 1-2 years in customer service/office environment |
Triage reviews all paperwork submitted with patient samples to ensure all required information for testing is received. They enter the patient’s insurance information into the database application and determine if the patient’s insurance requires additional documentation/processing for testing to be covered. The ability to focus on quality is crucial in this role. | 7/6/2019 |
| 14807 | Molecular Templates Austin, TX Research Associate BS/BA in life sciences Exp: 1 or more years in research |
Molecular Templates is seeking a highly-motivated and skilled Research Associate to support research and development activities. The position will be primarily responsible for ETB protein production and analysis in accordance to established protocols, and performing general laboratory duties, including solution and media prep, labware sterilization, ordering supplies, and maintaining inventory and basic laboratory equipment. This position will require excellent technical, analytical, time management and organizational skills, along with adherence to written and verbal instructions and accurate and timely completion of documentation. | 7/6/2019 |
| 14808 | Molecular Templates Austin, TX Manufacturing Associate BS/BA in life sciences Exp: 1 or more years in lab setting or protein purification |
Molecular Templates is seeking an experienced and highly-motivated professional to support downstream processing for manufacturing activities. This position will perform functions related to production and manufacturing operations, including routine protein purification, equipment maintenance checks and calibration, data management, and assist in review and development methods and procedures to control or modify the manufacturing process. This position will also aid in identifying continuous process improvement areas. | 7/6/2019 |
| 14809 | Molecular Templates Austin, TX Research Associate, Downstream BS/BA in life sciences Exp: 1 or more years in lab setting or protein purification |
Molecular Templates is seeking a highly-motivated and skilled Research Associate to support downstream processing for Protein Sciences. This position will perform functions related to production of pre-clinical drug product and early-stage process development for protein sciences, including routine protein purification, equipment maintenance checks and calibration, data management, and assist in review and development methods and procedures to control or modify the process. This position will also aid in identifying continuous process improvement areas. | 7/6/2019 |
| 14810 | Molecular Templates Austin, TX Research Associate, Upstream BS/BA in life sciences Exp: 1 or more years in lab setting or protein expression |
Molecular Templates is seeking a highly-motivated and skilled Research Associate to support upstream processing for Protein Sciences. This position will perform functions related to production of pre-clinical drug product and early-stage process development for protein sciences, including routine protein expression, equipment maintenance checks and calibration, data management, and assist in review and development methods and procedures to control or modify the process. | 7/6/2019 |
| 14811 | Molecular Templates Austin, TX Research Associate BS/BA in life sciences Exp: 1 or more years in biological research lab |
Molecular Templates is seeking a highly-motivated and skilled Research Associate to support research and development activities. This position will be primarily responsible for maintaining cell lines, conducting cellular cytotoxicity assays and performing flow cytometry in accordance to established protocols, and performing general laboratory duties, including washing glassware, ordering supplies, and maintaining inventory and basic laboratory equipment. | 7/6/2019 |
| 14812 | MeritMedical South Jordan, UT Engineer I MS in engineering or related Exp: 0-2 years |
This Engineer I could be working in the wafer fabrication, wafer dicing, and/or electronic assembly areas. Performs routine technical work requiring the application of standard techniques, procedures, and criteria in carrying out engineering tasks. Uses limited amounts of discretionary judgment in making decisions regarding technical alternatives. Performs work of some higher technical level for training purposes, and work is screened to ensure correct application of scientific principles. Works on special projects, writes ECN's, and may create prototypes under general direction. | 7/5/2019 |
| 14813 | MeritMedical Malvern, PA Quality Assurance Technician-TEMP AS/AA Exp: 1 year or more |
Performs routine quality technical assignments including data entry, storing master documents and issuing documents to authorized entities. Audits and inspects the production process to confirm that Device History Records are completed according to Device Master Record/QSR/GMP regulations. Audits and inspects finished products to ensure that it conforms with Device History Records and applicable specification and procedures. Initiates, identifies (labels) and ensures closure of NCMR's. Enters information into NCMR database. | 7/5/2019 |
| 14814 | MeritMedical South Jordan, UT Material Handler I HS Diploma/GED Exp: 3 months warehouse experience |
Responsible for pulling parts from the warehouse and seeing that line production workers have the raw materials they need to perform their jobs. Obtains parts from the warehouse for use in production and verifies the part's lot number to ensure that the proper materials are used. Pulls supplies for assembly workers and ensures that supplies are stocked and readily available for assembly workers. Puts the parts in production bins for easy handling by the production workers. | 7/5/2019 |
| 14815 | MeritMedical South Jordan, UT Technician II - Weekend Shift AS/AA Exp: 1 year or more |
Performs routine technical tasks including assembling or constructing simple or standard equipment or parts, and may service or repair simple instruments or equipment. Conducts a variety of tests using established and clearly defined methods. Prepares test specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Extracts engineering data from various prescribed sources and processes the data following well-defined methods, then presents the data in prescribed form. | 7/5/2019 |
| 14816 | MeritMedical South Jordan, UT Packager HS Diploma/GED Exp: 6 months or more work experience |
Packages and labels products, inspects products to ensure that the number and type of product matches the label, and records the products packaged. Boxes manufactured products, checking products to ensure that they are the correct lot number and amount to be put in the box, and that the label matches the lot number and amount. Checks boxes to make sure that they are properly secured and that they are clean and neat in appearance. Obtains the correct labels for products to be boxed, matching labels with goods ordered. | 7/5/2019 |
| 14817 | Merz Franksville, WI Engineer – Calibration and Reliability BS/BA in physicis, electrical engineering, electronics or related Exp: 1 year or more in calibration/reliability |
The Engineer – Calibration and Reliability is mainly responsible for the integrity of the calibration process and to ensure all documentation and procedures are up-to-date and cover all regulatory requirements. Other responsibilities include the improvement of asset reliability through predictive maintenance, analysis of data collected, risk assessments or other reliability related techniques or processes. | 7/5/2019 |
| 14818 | Merz Franksville, WI Biomedical Engineer BS in biomedical engineering, engineering or life sciences Exp: 0-5 years in engineering/biotech |
The Biomedical Engineer is responsible for facilitating the transfer, scale-up, and validation of new and improved product designs and processes into manufacturing. Also responsible for assisting and providing technical product support for other functions including regulatory, quality, manufacturing, clinical, marketing and sales. | 7/5/2019 |
| 14819 | Merz Mesa, AZ Engineer - NPI BS/BA in ME, IE, EE or other engineering Exp: 1-5 years in product design/development/manufacturing |
Responsibilities include: Drive efforts to design, develop, validate, and continuously improve manufacturing processes. Develop & define production control methods to monitor process output and establish critical supplier metrics. Define and coordinate the design and development of manufacturing fixturing and test equipment. Coordinate with R&D to optimize the design for manufacturing and reliability. | 7/5/2019 |
| 14820 | Merz Franksville, WI Quality Control Associate I BS/BA in physical sciences or related Exp: 1-3 years in quality |
This role is responsible for executing daily activities in the QC Laboratory including support testing for the production of Merz North America product. Oversee and/or assist with tasks related to the activities associated with operation of Merz Quality System and as directed by Quality Management. Support all activities related to analytical assessment of Merz NA products and the manufacturing environment. Advise Quality Assurance, Manufacturing and MS&T departments on matters related to analytical testing and support. Provide direct support to Quality Assurance personnel regarding operation of the department and Quality System. | 7/5/2019 |
| 14821 | Merz Mesa, AZ Regulatory Affrs Assoc BS/BA in sciences or healthcare Exp: 1 or more years in regulatory |
The Regulatory Affairs Associate supports the regulatory activities for development projects including new products and life cycle management. This includes assisting with regulatory strategies and timelines as well as the development and implementation of submissions under the direction of a line manager. With support from Regulatory Affairs Manager, provide ongoing support to cross functional teams to provide regulatory strategies during product development. | 7/5/2019 |
| 14822 | MSD Rockville, MD Production Control Tech I BS/BA in life sciences Exp: 1 or more year in biotech lab or manufacturing |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. The position will help standardize and improve documentation, manufacturing procedures and processes to increase production efficiency and ensure best practices are followed. The position will also help implement new products, projects and processes within Manufacturing Operations. Some degree of professional latitude, creativity and self-management is expected. | 7/5/2019 |
| 14823 | Metabolon Durham, NC Sofware Development Engineer BS/BA in computer sciences or related STEM Exp: 0-2 years in software development |
We are looking for exceptional self-starters who take pride in utilizing best practices to build scalable, maintainable software to provide our customers with the best user experience. We look for talented software engineers who believe in our mission, find meaning to the work that we do, and hold themselves accountable for deadlines and high-quality deliverables | 7/5/2019 |
| 14824 | Mevion Medical Systems Littleton, MA Software Engineer I BS/BA in computer sciences, electrical or computer engineering Exp: 0-3 years in C/C++ programing |
Responsibilities will include various system engineering activities for the PTS-250 development, including, but not limited to: 1. Responsible for design, development, integration and testing of various tasks in support of the PTS Software development effort. 2. Work with engineers from the various project teams in order to develop the PTS-250 software. 3. Work with quality engineering to develop test plans. 4. Responsible for design documentation.Responsibilities will include various system engineering activities for the PTS-250 development, including, but not limited to: 1. Responsible for design, development, integration and testing of various tasks in support of the PTS Software development effort. 2. Work with engineers from the various project teams in order to develop the PTS-250 software. 3. Work with quality engineering to develop test plans. 4. Responsible for design documentation.Responsibilities will include various system engineering activities for the PTS-250 development, including, but not limited to: 1. Responsible for design, development, integration and testing of various tasks in support of the PTS Software development effort. 2. Work with engineers from the various project teams in order to develop the PTS-250 software. 3. Work with quality engineering to develop test plans. 4. Responsible for design documentation. | 7/5/2019 |
| 14825 | Mevion Medical Systems Littleton, MA Commissioning & Support Engineer BS/BA in physics, electrical engineering, computer science or related Exp: 1 or more years |
The Commissioning & Support Engineer responsibility is two-fold: it includes both on-site, hands-on installation work and remote product support. The role of commissioning engineer involves frequent travel to customer sites to configure and commission the S250-series cyclotrons under installation. During remote weeks or between installs, this role functions more like product support, responsible for providing business critical technical support to other commissioning engineers, installers, field service engineers and customers to help ensure the highest operational status possible. | 7/5/2019 |
| 14826 | Analytical Lab Group Concord, CA Laboratory Technician AS/AA in microbiology or related Exp: 0-1 years in pharma/biotech |
The technician's main duties are to ensure timeliness of testing, meeting client requirements. The technician must provide services that are compliant to the ALG-West Coast Quality Manual, client requirements and regulatory requirements as applicable such as ISO/IEC 17025:2017, USP, EU, GLP, GMP, FDA and ICH guidelines. | 7/5/2019 |
| 14827 | Analytical Lab Group Concord, CA Environmental Monitoring Technician AA or BS in microbiology or related sciences Exp: 1 or more years in GMP |
Analytical Lab Group's West Coast location is looking for laboratory technicians to perform environmental monitoring at client facilities and microbiology testing in the microbiology lab. This is a full-time position. The schedule will be Monday-Friday, 7 a.m. to 3:30 p.m., but you must be able to work flexible hours, including different shifts and weekends. At this time, the starting hour is 5 a.m. and will require OT. | 7/5/2019 |
| 14828 | Idex Corporation Shelby , NC Production Associate - Material Handler HS Diploma/GED Exp: 1 or more year in manufacturing |
A Production Associate is a multi-skilled employee that will perform a variety of duties to support the assembly of rescue tools and other products. Production Associates will perform a variety of activities including (but not limited to) material handling, stocking parts, quality inspections, and packaging products for shipping. Responsible for maintaining established quality standards while ensuring a safe and clean work environment. | 7/5/2019 |
| 14829 | Micropoint Santa Clara, CA Quality Control Associates MS in chemistry, biology or related Exp: 0-2 years |
We are looking for highly motivated QC Associates (two openings) to join our quality team. These positions are responsible for participating as team members in a laboratory environment for finished product/or development programs focused on the goal of testing and releasing the immunoassays found in Micropoint's in-vitro diagnostic products for point-of-care (POC) testing. | 7/5/2019 |
| 14830 | Micropoint Santa Clara, CA Manufacturing Operators HS Diploma/GED Exp: 0-2 years in food/pharma/diagnostics manufacturing |
There are two openings. These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the company's disposable test cartridges. Follow written procedures for set-up, operation, and clean up of manufacturing equipments, final assembly, and packaging. Responsible for manual tasks including, pipette solution, pouch and box labeling, product inspection. Prepare materials used in the cartridge production process. | 7/5/2019 |
| 14831 | Microvention Aliso Viejo, CA Engineer I, R&D BS/BA in related field Exp: 0-3 years |
The Engineer I, R&D supports development of medical device products with work including writing or verifying specifications, designing new products, fixtures, test processes, equipment and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Job Duties: Develop new product concepts and products. Engineering design and process development. Generate intellectual property, write invention disclosures. etc. | 7/5/2019 |
| 14832 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, chemical engineering or related Exp: 0-4 years |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Ensure quality throughout the process. Assure you are adequately trained to perform tasks/assignments. Perform routine assays, processes and/or unit operations. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). | 7/5/2019 |
| 14833 | Merck KGaA St. Louis, MO Planning & Scheduling, Specialist BS/BA in business, mathmatics, supply chain, or related Exp: 0-1 years |
At MilliporeSigma the Planning & Scheduling Specialist reviews demand plans at a global and local level including adjusting forecast and safety stock parameters. He/she will also work with the sales group to incorporate customer demands into the planning systems and will develop operational schedules to meet customer service objectives and support sales growth plans at the lowest overall inventory costs. The specialist will also develop, test and execute models for scheduling operation and lead and/or assist process improvement initiatives. In addition, he/she will review long term plans to ensure capacity requirements are understood and met and will compile reports and metrics to ensure business has proper feedback loops on performance to objectives. | 7/5/2019 |
| 14834 | Merck KGaA Rockville, MD Associate Scientist 1 BS/BA in life sciences Exp: 0-2 years |
Perform all routine and relevant laboratory techniques in compliance with BioReliance regulatory standards. Maintain and operate all laboratory equipment with some troubleshooting, as required. Perform various cell culture operations for biosafety testing. Maintains thorough records in addition to peer review of batch records. Responsible for generating deviations as required and participating in resolving investigations with support of other team members. Maintains a standard up keep of the facility through daily cleaning. Actively performs equipment and general housekeeping daily checks and notify relevant personnel of any issues. Initiates and completes projects independently, including troubleshooting during routine laboratory activities. | 7/5/2019 |
| 14835 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, chemical engineering or related Exp: 0-4 years |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Ensure quality throughout the process. Assure you are adequately trained to perform tasks/assignments. Perform routine assays, processes and/or unit operations. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). | 7/5/2019 |
| 14836 | Merck KGaA Sheboygan Falls, WI Procurement Rep 1 HS Diploma/GED Exp: 1+ year office experience |
The purpose of this position is to Initiate and expedite the transfer of inventory from and to related parties. Ensure that all materials, equipment and tools are available for production and maintenance of site processes. Solicit price and delivery information from vendors, enters into computer files and communicates to appropriate departments. Coordinate with other departments the procurement of tools, materials and equipment. | 7/5/2019 |
| 14837 | Merck KGaA Bedford, TX R&D Analytical Lab Technician BS/BA or AS/AA Exp: 1+ year chemistry experience |
Must have good laboratory habits and be able to follow SOPs, procedures and protocols. Able to multi-task, handle routine as well as non-routine requests and assist other members of the group as required. Familiar with established laboratory procedures. Able to carry out experiments under close supervision. Possesses excellent record keeping skills, good written and verbal communications skills, and interacts effectively with peers and with people outside of the group. Able to work effectively with others to complete collaborative projects. | 7/5/2019 |
| 14838 | Merck KGaA Carlsbad, CA Manufacturing Technician 1 BS/BA or HS Diploma Exp: HS: 6 months, BS/BA: 0 year |
The Manufacturing Technician I position will work in a cleanroom environment and adhere to cGMP batch records and SOPs to support the manufacturing of viral vector products. Employees will support projects in conjunction with other GMP Manufacturing personnel (Leads, Supervisors, Managers). Employees are expected to prepare suites for manufacturing, to document deviations, and to operate in a safe and compliant manner. | 7/5/2019 |
| 14839 | Lentigen Technology Gaithersburg, MD R&D Molecular Biology Associate MS in molecular biology, immunology, or related Exp: 0-2 years |
You will use Lentigen’s expertise in lentiviral vector technology to analyze the biology of immune effector cells, stem cells and immortalized cell lines modified by lentiviral transduction. Furthermore, the unique duties of this position will allow you to master state of the art research and development techniques in molecular biology, lentiviral technology, genomics and immunology to make valuable contributions in keeping Lentigen Technologies, Inc. at the cutting edge of biomedical research. | 7/5/2019 |
| 14840 | Miltenyi Biotech Sunnyvale, CA Process Development Associate BS/BA in life sciences Exp: 0-2 years |
You will apply your GLP/GMP experience to perform and maintain cell cultures using aseptic techniques. Ideally, you will be able to order materials and maintain inventory with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical cell and gene therapy products. In addition to your primary responsibilities, you will document activities for reproducibility, clean and maintain laboratory equipment and support team members as needed. | 7/5/2019 |
| 14841 | Miltenyi Biotech Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years GMP environment |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. | 7/5/2019 |
| 14842 | Miltenyi Biotech Auburn, CA Logistics Associate HS Diploma/GED Exp: 1 or more year related experience |
As a member of the Miltenyi Biotec team, you will help ensure that the shipping and receiving process runs efficiently for our growing biotechnology organization. You will prepare and process inventory using your Enterprise Resource Planning (ERP) and shipping systems knowledge. In addition, you will record and receive incoming shipments according to established SOPs, as well as prepare and process shipments according to international regulations. There will also be occasion for employing hand-trucks and forklifts in order to move and store certain articles during routine inventory maintenance. | 7/5/2019 |
| 14843 | Miltenyi Biotech Auburn, CA Accounting Associate AS/AA Exp: 1-3 years in corporate business/accounting functions |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. | 7/5/2019 |
| 14844 | Meridian Bioscience Memphis, TN Quality Systems Software Engineer BS/BA in communications, computer science or related Exp: 0-2 years |
The Quality Systems Software Engineer position at Meridian Bioscience within the Life Science Quality Assurance department supports the Quality System by developing and maintaining electronic document and data management systems. The Quality Systems Software Engineer works with cross functional teams to identify areas that can be streamlined or improved by implementing processes that meet regulatory requirements and standards associated with electronic data management. The Quality Systems Software engineer.is responsible for application systems administration within the scope of Quality Systems. This includes working with cross functional teams to identify areas that can be streamlined or improved by implementing documentation processes that meet regulatory requirements and standards for electronic documentation, developing electronic form records, document management and workflow processes, and authoring supporting documentation including but not limited to validation protocols and reports and verification test methods and procedures. | 7/4/2019 |
| 14845 | Meridian Bioscience Cincinnati, OH Accounts Receivable Associate HS Diploma/GED Exp: 1 year in credit/collections |
Assist the Credit Department with wire and lock box processing, cash posting and collections. Electronic billing tasks which includes invoicing customers for shipments via email and invoice entry into customer portals. Monitoring the Accounts Receivable Email box and responding to customer requests for invoice copies and statements. Maintaining customer contact data within our collection software. Collecting and maintaining all customer sales tax documentation within Infor system. Generate and maintain rules in Cforia software system for monthly collection letters. | 7/4/2019 |
| 14846 | Meridian Bioscience Cincinnati, OH Material Handler I HS Diploma/GED Exp: 1 year of warehouse experience |
The Material Handler transports all types of materials within MBI. Transports materials to the proper departments or destination by driving, carrying, pushing or hand truck. | 7/4/2019 |
| 14847 | Merieux NutriSciences Minnetonka, MN Laboratory Assistant HS Diploma/GED Exp: 0 years |
We are currently seeking a Lab Assistant to provide assistance to our technicians and scientists. Responsibilities include: Carry out a number of procedures including preparing samples for analysis, sterilizing equipment, and general cleaning duties. Maintain working order of equipment and supplies necessary to perform analysis of food samples. Work closely with other team members and with the support of a department supervisor | 7/4/2019 |
| 14848 | Merieux NutriSciences Madison , WI Sample Receiving Technician HS Diploma/GED Exp: 0 years |
Work as a member of a team to receive and log in client samples to prepare them for analysis. Review samples and documentation to assign identification numbers and enter data into our tracking system. Prepare packages for shipping and pick up by vendors. Contact clients when necessary to confirm information about test codes and sample contents. Achieve accurate, timely and consistent results to ensure samples are processed correctly | 7/4/2019 |
| 14849 | Merieux NutriSciences Salida, CA Sample Receiving Technician HS Diploma/GED Exp: 0 years |
Work as a member of a team to receive and log in client samples to prepare them for analysis. Review samples and documentation to assign identification numbers and enter data into our tracking system. Prepare packages for shipping and pick up by vendors. Contact clients when necessary to confirm information about test codes and sample contents. Achieve accurate, timely and consistent results to ensure samples are processed correctly | 7/4/2019 |
| 14850 | Merieux NutriSciences Allentown, PA Receiving Tech HS Diploma/GED Exp: 0 years |
Work as a member of a team to receive and log in client samples to prepare them for analysis. Review samples and documentation to assign identification numbers and enter data into our tracking system. Prepare packages for shipping and pick up by vendors. Contact clients when necessary to confirm information about test codes and sample contents. Achieve accurate, timely and consistent results to ensure samples are processed correctly | 7/4/2019 |
| 14851 | Merieux NutriSciences Crete, IL Chemist I BS/BA or AA/AS in chemistry or related Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. This position reports to the Supervisor of Chemistry. | 7/4/2019 |
| 14852 | Merieux NutriSciences Crete, IL Data Entry Specialist, Administrative HS Diploma or higher Exp: 1-2 years in data entry |
We are looking for data entry specialists with 1-2 years of experience in data entry. Fast paced work environment will require at least 60 WPM and moderate computer skills to fulfill job duties | 7/4/2019 |
| 14853 | Merieux NutriSciences Madison , WI Laboratory Tech-Sample Receiving HS Diploma or higher Exp: 0 years |
Work as a member of a team to receive and log in client samples to prepare them for analysis. Review samples and documentation to assign identification numbers and enter data into our tracking system. Prepare packages for shipping and pick up by vendors. Contact clients when necessary to confirm information about test codes and sample contents. Achieve accurate, timely and consistent results to ensure samples are processed correctly | 7/4/2019 |
| 14854 | Reckitt Benckiser Parsippany, NJ Performance Marketing Associate, Comms & Content BS/BA or MBA Exp: 1-2 years |
You will be responsible for identifying and driving all digital content creation (Amazon A+/WebCollage, optimized copy, enhanced images and videos, Brand Store pages and Brand campaigns) for new and existing items across key brands. Assist sales teams for eTail such as Amazon, Walmart.com, Target.com, Costco.com to ensure content is optimized to achieve “best in class” ratings, using scorecards provided by tools such as Clavis as well as key customer dashboards. Research competitive data to understand current industry trends in order to stay competitive and develop best practices for E-Commerce content as it pertains to site merchandising and the online user experience. You are supposed to represent the end consumer and bring in their perspective and insights to add value within the broader e-commerce team. You would be the main point of contact for the various Brand teams and would work closely in understanding their brand strategy and bringing it to life within the ecommerce world. etc. | 7/2/2019 |
| 14855 | Reckitt Benckiser Parsippany, NJ eCommerce Supply Fulfilment, Business Analyst unspecified Exp: Entry level or 1-2 years |
RB is driving aggressive growth in direct to consumer, E-Commerce globally. We are looking for an innovative individual to overdrive the online business with a unique combination of supply management, back office fulfilment operation maintenance and enhancements. The BA is key to the support and delivery of these overall team objectives: Responsible for developing and operating upstream end to end seamless supply chain flow for RBNA Health routes to market. Supply planning supervision is expected to ensure top level Service toward all D2C customer or consumer. Focusing on US. Manage, lead and develop robust S&OP process to allow no business disruption as well as liabilities – key stakeholder coordination is key (in market E commerce sales and marketing team, Finance, Manufacturing). Ensure Global supply processes are respected while developing new potential specific process requiring higher speed for Ecommerce. Define Logistics Strategy with key supply contact in US and CA sourcing countiresn– PNL monitoring and logistics cost optimization as key (freight mode, warehousing, potential D2C operation expansion). etc. | 7/2/2019 |
| 14856 | Reckitt Benckiser Parsippany, NJ Performance Marketing Analyst BS/BA Exp: 1+ years |
Activation practitioner with experience in the media/search marketplace, who is eager to have immediate impact on RB E-Business team in its activation and optimization practice. Energized by the development of data architectures to drive performance along with executing dashboards that drive clear analysis and insights on in-market media results. Eager to create meaningful vendor partnerships & act as daily trader within self-service media platforms. ‘Hands on Keyboard’ operational activation & management of e-commerce Search/SEM strategy with stewardship of keyword, bid and pacing management Maintain relationships across Amazon AMS, AMG & Criteo Stewardship of go-to-market marketing approach across Bricks & Clicks customers, inclusive of activation of display & SEM campaigns. etc. | 7/2/2019 |
| 14857 | Reckitt Benckiser Hillsborough, NJ Manufacturing Technician, Weekdays 1st shift (7:15am-3:30pm) unspecified Exp: Recent graduates |
The Manufacturing Tech is responsible for both running production lines when needed and making maintenance and technical decisions with exceptional knowledge of how the decisions will impact financial, quality and safety metrics; understanding and adhering to guidelines in the employee handbook and complying with regulatory requirements, company / plant policies, procedures, and rules in his/ her area of responsibility. The Manufacturing Tech must be able to independently perform most assignments. This is a skilled position that requires prior experience with packaging lines, equipment and processes. etc. | 7/2/2019 |
| 14858 | Reckitt Benckiser Salt Lake City, UT Plant Finance Analyst (Grad Program) BS in accounting preferred Exp: 2019 graduates |
We are looking for graduating students to join our RB Finance Graduate Development Program. You may do rotations through: Supply Finance, Commercial Finance and Accounting. Responsibilities: Collect, process, verify, and report accounting related information. Perform professional analytical and management to support work assignments. Assist in preparing monthly financial reports, developing and/or utilizing spreadsheets, databases and other computer applications. Process specialized information, reports, and forms for fees, billing, project tracking, etc. Enter information reports into a financial accounting system. Other financial, accounting, and information system related tasks are to be performed as assigned. etc. | 7/2/2019 |
| 14859 | Reckitt Benckiser Evansville, IN Early Innovation Scientist, Analytical Sciences BS/MS in chemistry or related Exp: Recent graduates |
Proactively support early innovation analytical and human milk assessments for front end innovation initiatives. Active participant on early innovation project teams as an Analytical Sciences and Human Milk Research representative who delivers rapid analytical technology and human milk assessments, timely responses regarding analytical and human milk research questions, project deliverables and on-going analytical research support. Supports further understanding of human milk through ability to research and synthesize published human milk research and utilize new technologies and instrumentation. Contributes to technical hypotheses regarding analytical research and human milk capabilities and carries out protocols to test those hypotheses, with possible hands-on analytical lab involvement. Builds strong internal and external collaborations and coordinates scientific research to drive innovation initiatives. Effectively communicates scientific knowledge and information to technical and non-technical audiences at multiple levels through a variety of internal and external facing formats. Represents MJPNI at scientific conferences and external meetings to communicate scientific insights and understandings. | 7/2/2019 |
| 14860 | Reckitt Benckiser Evansville, IN Innovation Method Development Scientist, Analytical Sciences BS/MS in chemistry or related Exp: Recent graduates |
Proactively identifies and executes strategic analytical method development and validation initiatives to support early innovation projects, human milk research, and key quality objectives. Active participant on project teams as an Analytical Sciences representative who delivers timely responses regarding analytical questions, project deliverables, and on-going analytical support. Identifies areas of improvements for analytical methodology through utilization of new technologies and instrumentation, implementation of method validation and transfer practices, and effective networking with the internal MJN analytical community as well as external experts. Contributes to technical hypotheses regarding analytical capabilities and develops protocols to test those hypotheses. Efficiently creates and executes method validation protocols to ensure developed methods are compliant against all internal criteria. Performs instrument maintenance and repair support while building knowledge and understanding of troubleshooting methodology and instrumentation issues. Effectively communicates scientific knowledge and information to technical and non-technical audiences at multiple levels through a variety of internal and external facing formats. | 7/2/2019 |
| 14861 | Regeneron Tarrytown, NY Clinical Study Specialist (Inflammatory & Immunology) MS Exp: 1-2 years |
The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs). They: Organizes and delivers analyzable reports and metrics to the clinical study lead. Schedules and coordinates meetings, prepares agendas, presentation materials and minutes for clinical study team meetings and other study related meetings. Collates data for assessments such as feasibility and site selection and reviews site usability database. etc. | 7/2/2019 |
| 14862 | Regeneron Tarrytown, NY Associate 1, Clinical Logistics BS/BA Exp: 1+ years |
The Clinical Logistics Associate I provides support to the Clinical Logistics group and IP distribution process for one or more clinical trials. Activities are performed on time, within budget and with good quality, in compliance with Regulatory Authorities’ regulations / guidelines and Regeneron SOPs / WPDs. Contributes to ongoing process improvement initiatives. This role applies to internally sourced studies and/or CRO/Partnered studies. Interacts with clinical trial managers, as well as staff from quality, clinical compliance, and IOPS (CMC, external manufacturing, stability). etc. | 7/2/2019 |
| 14863 | Regeneron Tarrytown, NY TEMP Clinical Study Specialist (Oncology) MS Exp: 1-2 years |
The Temp - Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The Temp - CSS may be assigned to support the execution of one or more studies across a program. The Temp - CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The Temp - CSS will support internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs). Responsibilities: Organizes and delivers analyzable reports and metrics to the clinical study lead. Schedules and coordinates meetings, prepares agendas, presentation materials and minutes for clinical study team meetings and other study related meetings. etc. | 7/2/2019 |
| 14864 | Regeneron Rensselaer, NY Biotech Production Dispensing Technician AAS Exp: 0-2 years |
Summary: Performs all tasks necessary for the manufacturing dispensing operations. Essential Duties and Responsibilities include, but are not limited to, the following: Includes all aspects of biotech production activities related to raw material dispensing. Ensures that raw materials are dispensed as specified in Batch Sheets or Manufacturing Records to support manufacturing operations. Works with manufacturing process areas and manufacturing inventory group to schedule lots of raw materials to be dispensed. Reviews, edits, completes, and revises completed batch records (if applicable), Logbooks, and SOPs in accordance with cGMP standards and compliant with written procedure. etc. | 7/2/2019 |
| 14865 | Regeneron Tarrytown, NY Process Development Associate II - Mammalian Cell Culture Medium Dev. BS/MS in chemical or related engineering Exp: 0-2 years |
The Cell Culture and Medium Development Group within Preclinical Manufacturing and Process Development is looking for a motivated person to assist in medium development for mammalian cell culture processes. He/she will perform studies at a benchtop scale to develop cell culture medium that improves cell growth, cell productivity, and/or product quality. In this role, the individual will perform innovative cell culture experiments, high-throughput model development, small-scale bioreactor development, and literature searches. The ability to design experiments, statistically interpret results, and communicate findings is required. etc. | 7/2/2019 |
| 14866 | RTI Surgical Alachua, FL Donor QA Associate AA Exp: 1 year |
POSITION SUMMARY: Obtain, compile, track, review, file and disposition accurate and complete donor records (paper and electronic) to support applicable regulations, standards and departmental procedures for donor eligibility determination in a timely manner. Disposition donors in electronic system for release into production, rejection or Medical Director request for additional information. Develop and maintain effective working relationships with recovery agencies and other entities providing donor records to facilitate timely submission of accurate and complete required records. Act as departmental liaison to both internal and external customers to provide requested donor related information and/or resolve issues as requested. Comply with all applicable regulations, standards, company policies and departmental procedures. Support company and departmental quality and business objectives and initiatives. Provide information to develop and monitor quality and business metrics as requested. | 7/2/2019 |
| 14867 | RTI Surgical Alachua, FL Material Tech 1 HS Diploma or equivalent Exp: Entry level |
The Materials Tech 1 position at RTI represents an entry level function. Employees will develop technical skills in their assigned areas, an understanding of the rules and regulations that RTI administers, and the basic operating approach at RTI including: reading, understanding, and following work instructions; working in a team environment; and learning to work with minimal supervision. POSITION SUMMARY: Performs tissue processing activities that produce the highest level of quality and yield outcomes in accordance with applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs). Responsible for accurately processing tissue products and meeting production schedules. etc. | 7/2/2019 |
| 14868 | RTI Surgical Alachua, FL Tissue Processing Tech 1 HS Diploma or equivalent Exp: Entry level |
The Tissue Tech 1 position at RTI represents an entry level function. Employees will develop technical skills in their assigned areas, an understanding of the rules and regulations that RTI administers, and the basic operating approach at RTI including: reading, understanding, and following work instructions; working in a team environment; and learning to work with minimal supervision. POSITION SUMMARY: Performs tissue processing activities that produce the highest level of quality and yield outcomes in accordance with applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs). Responsible for accurately processing tissue products and meeting production schedules. etc. | 7/2/2019 |
| 14869 | Rubryc Therapeutics San Carlos, CA Executive Assistant BA/BS Exp: 1-3 years |
The Executive Assistant reports to the CEO and will play a key support role as the Company proceeds through important developmental milestones and growth spurts in the coming years. RubrYc’s Executive Assistant will act as a crucial coordinator of meetings and contact among executives, employees, service providers, vendors, clients, investors, advisors, and other stakeholders. The Executive Assistant will manage information flow amongst and between these individuals and organizations accurately and efficiently.The Executive Assistant will have important operational roles including supporting expense reporting and reimbursement/payment, maintaining office supply inventory for the Company and laboratory materials supply inventory for R&D teams; interfacing with facilities and IT service providers; coordinating Executive Management Team calendars, arranging for travel and transportation, and managing team and Company meeting schedules. etc. | 7/2/2019 |
| 14870 | Salix Pharmaceuticals Bridgewater, NJ Salix Inside Sales Associate BA/BS in business or related Exp: Recent graduates |
The Salix Inside Sales Associate program offers a unique opportunity for recent college graduates who are interested in a fast start to an exciting career in medical/medical device sales. We are seeking candidates who are highly competitive, have a strong work ethic and are motivated to accelerate their position in a company currently launching several new and innovative products into the GI marketplace. Those accepted into this exclusive program will relocate to Bridgewater, NJ for approximately 12 months. During the 12 months Sales Associates receive intensive training on: Products, Selling Skills, and Industry & Territory Management. Upon successful completion of the 12-month training program, Sales Associates ready for the field will be eligible to apply to any open Salix Territory Manager positions. Sales Associate pay, bonus and benefits are competitive. Upon placement into a field sales territory the Sales Associate is provided with a company car and necessary tools to manage a territory - including an iPad and iPhone. Some relocation assistance may be available depending on relocation distance. etc. | 7/2/2019 |
| 14871 | SAMDI Tech Chicago, IL Research Assistant (Full-time) BS in biology, chemistry, or related Exp: 0-3 years |
We are seeking a highly motivated and skilled scientist to join our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include supporting the preparation of reagents and materials for running biochemical assays, assisting in executing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, integrating automated liquid handling, and supporting fundamental laboratory functions. | 7/2/2019 |
| 14872 | SAMDI Tech Chicago, IL Research Associate- Biochemical Assay Specialist (Full-time) MS in biology, chemistry, or related Exp: 1-3 years |
We are seeking a highly motivated and skilled scientist to join our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include handling and processing of reagents and materials for running biochemical assays, designing and performing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, take a project leadership role on multiple targets/enzymes, integrating automated liquid handling, and writing and maintaining Standard Operating Protocols (SOPs). | 7/2/2019 |
| 14873 | Samumed San Diego, CA DMPK, Research Associate BS in life, chemical sciences or related Exp: 0-4 years |
Samumed has an immediate opening for a Research Associate to perform bioanalytical analysis from in vivo pharmacokinetic/pharmacology studies in a variety of matrices and assist in developing novel bioanalytical methods using LC/MS/MS. Specific Responsibilities: Perform bioanalytical extractions of test article and metabolites from biological matrices. Operate, troubleshoot, and maintain LC-MS/MS and other analytical equipment. Generate high quality data in timely manner to inform project teams. Planning and executing scientific experiments as required. Analyzing and documenting experimental data in electronic notebooks in a timely and accurate manner in accordance with the company guidelines. Performing additional general duties to support the safe and efficient operation of the laboratory as required. Samumed has an immediate opening for a Research Associate to perform bioanalytical analysis from in vivo pharmacokinetic/pharmacology studies in a variety of matrices and assist in developing novel bioanalytical methods using LC/MS/MS. Specific Responsibilities: Perform bioanalytical extractions of test article and metabolites from biological matrices. Operate, troubleshoot, and maintain LC-MS/MS and other analytical equipment. Generate high quality data in timely manner to inform project teams. Planning and executing scientific experiments as required. Analyzing and documenting experimental data in electronic notebooks in a timely and accurate manner in accordance with the company guidelines. Performing additional general duties to support the safe and efficient operation of the laboratory as required. | 7/2/2019 |
| 14874 | Sanofi Framingham, MA Senior Research Associate, Analytical Development I MS Exp: 0-2 years |
This position is within the Analytical Development group which develops, qualifies, and transfers analytical methods used for characterization of protein and gene therapeutics in early stage development (Phase I/II). We are seeking a highly motivated individual to participate in cGMP sample testing, as well as the development, qualification, and transfer of analytical methods, based on platforms such as enzymatic activity, gel and capillary electrophoresis, ELISA, and HPLC for the purposes of drug substance and/or drug product lot release and stability testing. Duties and Responsibilities: Perform method development and scientific procedures and experiments under minimal supervision. Plan and prioritize concurrent experimental procedures and document in an electronic lab notebook. Integrate, compile, analyze, and interpret data with minimal supervision. etc. | 7/2/2019 |
| 14875 | Sanofi Westborough, MA Stability Specialist BA/BS Exp: 1-3 years |
Executes stability programs to support product expiration dating, storage and handling, shipping and patient use in compliance with industry practices and regulatory requirements. Also participates in the Periodic Product Review (PPR) process. Responsibilities: Participate in monitoring stability storage conditions, submit stability samples to analytical laboratories when required and monitor laboratory test results. Participate in developing stability study protocols and in in establishing strategies for stability studies. Perform analysis of stability data and draft stability technical reports. Escalate unusual observations, deviations or any incidence of non-compliance with established protocols or procedures. Compile stability data for inclusion in regulatory submissions. Participate in the compilation of Periodic Product Review (PPR) reports. Participate directly with external departments (e.g. Manufacturing Science & Technology, External Supply Quality Assurance, and CMOs). etc. | 7/2/2019 |
| 14876 | Sanofi Allston, MA Quality Control Analyst I BS in life sciences discipline Exp: 1 year in a cGMP lab environment |
Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for CGMP operations. Various techniques are utilized in Quality Control including, HPLC, GC, Gel Electrophoresis and multiple types of spectrophotometry. Additional functions include raw material testing, stability testing, assay transfers and the qualification of new instrumentation utilized in the Quality Control laboratory. Position Overview with Key Responsibilities: Key Responsibilities may differ among employees with same job title and may change over time in accordance with business needs. This position is responsible for performing routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation. etc. | 7/2/2019 |
| 14877 | Sanofi Toronto, ON Packaging Technician, Day Shift Minimum 3 year college diploma in pharmaceutical technology Exp: 6+ months |
Sanofi Pasteur Limited is looking for motivated and results driven individuals to join our Filling and Packaging team as a Packaging Technician. Key responsibilities will include the following: 1. Monitor all tasks in packaging areas. 2. Maintain equipment in good condition. 3. Plan for training. 4. Ensure quality of the packaging process. 5. Provide training. etc. | 7/2/2019 |
| 14878 | Sanofi Toronto, ON Packaging Technician, Day Shift Minimum 3 year college diploma in pharmaceutical technology Exp: 6+ months |
Sanofi Pasteur Limited is looking for motivated and results driven individuals to join our Filling and Packaging team as a Packaging Technician. Key responsibilities will include the following: 1. Monitor all tasks in packaging areas. 2. Maintain equipment in good condition. 3. Plan for training. 4. Ensure quality of the packaging process. 5. Provide training. etc. | 7/2/2019 |
| 14879 | Sanofi Swiftwater, PA Biological Sales Associate: National Sales Network (NSN) Conference 2019 BA/BS Exp: 0-2 years |
This position is part of the Biological Sales Associate Program. This program consists of 3 developmental phases: in-house training, outbound sales responsibility based at our home office in Swiftwater, PA and a field externship period where the selected candidate would backfill one of our Vaccine Specialist positions anywhere in the US. The entire program lasts approximately 12 months with the ultimate goal of having the candidate earn a promotion to a permanent position as a Vaccine Specialist within our field sales force. This position requires that a candidate be willing to relocate to Swiftwater PA for the first half of their program and then be willing to relocate anywhere in the US upon completion. etc. | 7/2/2019 |
| 14880 | Sarepta Therapeutics Burlington, MA Research Associate II, Gene Therapy Process Development - In-Process Analytics MS in pharmaceutics, chemical engineering, chemistry, or related Exp: 0-3 years |
The Research Associate will support the development of Sarepta’s Gene Therapy platform. Working as a member of Gene Therapy group within Technical Operations department, he/she will support the implementation of in-process analytical test methods for use in the development of gene therapy products. The individual will collaborate with the Analytical Development team to support the adaptation of release test methods for use in-process, will execute established test methods to better characterize product and impurities over the course of development and will collaborate with process development scientists on the design and interpretation of studies. The individual may also work with external stakeholders in supporting evaluation of processes managed outside of the organization. etc. | 7/2/2019 |
| 14881 | Sarepta Therapeutics Burlington, MA Associate I, Gene Therapy Pilot Coordination BS Exp: 0-2 years |
The Associate I, Gene Therapy Pilot Coordination will help drive the development of Sarepta’s Gene Therapy platform. Working as a member of the Gene Therapy Pilot Team within Technical Operations he/she will be responsible for supporting scale-up studies and material production at a pilot scale within Sarepta’s internal laboratories. The Associate I, Gene Therapy Pilot Coordination will be responsible for documentation, product and sample inventories, as well as raw material and supply stocks. He/she will be expected to work in close collaboration with other Pilot Team members, as well as colleagues in the development and manufacturing organizations. | 7/2/2019 |
| 14882 | Sarepta Therapeutics Columbus, OH Laboratory Veterinarian Technician HS Diploma, AS/BS preferred Exp: 1-2 years |
Primary responsibilities Include: Handle, transfer, and distribute mice, supplies and waste as needed to and from work area(s). Proficient in IM, IV, IP administration techniques in lab animals. Clean cages and racks. Monitor the daily health and welfare of the animals according to IACUC guidelines. Coordinate with vendors and supervisors on operational, administrative and technical responsibilities. Responsible for overseeing procurement of animals and supplies, preventive maintenance of facility equipment. Strong written and verbal English communication skills. Ability to follow written and verbal instructions. Follows standard operating procedures and maintains recordkeeping pertaining to equipment operation, animal and supply inventories in accordance with federal and state guidelines and regulations. etc. | 7/2/2019 |
| 14883 | Sarepta Therapeutics Columbus, OH Research Associate I, Histology, Gene Therapy Research AS in chemical, physical, or biological science Exp: 1-3 years |
Sarepta Therapeutics is seeking a motivated individual with histology laboratory expertise/training. The qualified candidate will provide laboratory support of day-to-day GCP/GLP testing on muscle/nerve using complex histology methods in accordance with the requirements of approved protocols; maintains records of experiments; assists in analyzing data and prepares laboratory reports. This person may participate in development, GCP/GLP qualification, and validation of histology related assays to support clinical trials and clinical development decision-making. Primary responsibilities include: Performs routine and complex laboratory procedures in histology using frozen section techniques. Assist in the execution of GCP/GLP clinical study sample processing, staining and analysis using a variety of assay formats such as Histochemical special stains, Immunofluorescence and Immunohistochemistry. etc. | 7/2/2019 |
| 14884 | Sarepta Therapeutics Cambridge, MA Clinical Research Associate II, Translational Development BS in biochemisty or related field Exp: 1-2 years |
Sarepta Therapeutics is seeking a motivated clinical operations specialist with experience working in clinical operations and GCP/GLP environment for a clinical operations support role. The Research Associate (RA) will assist the Clinical Research Manager in interacting with the Clinical Operations group in the planning, execution and management of clinical samples. The RA will support the transfer of clinical samples from collaborators and CROs to Sarepta and third party storage facilities. He/She will work closely with the Clinical Research Manager to facilitate the training of international biopsy surgical sites and distribution of training materials. Additionally, he/she will take on a role in tracking training documentation across studies/research protocols. The candidate must exercise discretion and judgment in handling confidential information and will follow FDA regulations, ICH guidelines and GCP in all tasks. Strong organizational skills are required, as well as the ability to balance changing priorities. The role may involve occasional travel to oversee clinical sites or vendors. etc. | 7/2/2019 |
| 14885 | Regeneron Tarrytown, NY R&D Associate, VelocImmune (VI) Next MS Exp: 0+ years |
VelocImmune (VI) Next is a technology development group at Regeneron that invents and develops state-of-the-art tools for biologic drug discovery. We are seeking a motivated, highly organized researcher to support our investigations of new antibody and cell-based therapies. This is an opportunity for a researcher with strong molecular & cell biology skills to contribute to the development of industry-leading technologies and medicines. Responsibilities: Independently and as a team, conduct and support experiments. Investigating and develop new methodologies and technologies in molecular biology and biological therapeutics. Design, construct, and test DNA vectors, viral vectors, and cell-lines for in vitro and in vivo studies of candidate biologicals. Characterization of mice via NGS (next-generation sequencing) and flow cytometry-based phenotyping. etc. VelocImmune (VI) Next is a technology development group at Regeneron that invents and develops state-of-the-art tools for biologic drug discovery. We are seeking a motivated, highly organized researcher to support our investigations of new antibody and cell-based therapies. This is an opportunity for a researcher with strong molecular & cell biology skills to contribute to the development of industry-leading technologies and medicines. Responsibilities: Independently and as a team, conduct and support experiments. Investigating and develop new methodologies and technologies in molecular biology and biological therapeutics. Design, construct, and test DNA vectors, viral vectors, and cell-lines for in vitro and in vivo studies of candidate biologicals. Characterization of mice via NGS (next-generation sequencing) and flow cytometry-based phenotyping. etc. VelocImmune (VI) Next is a technology development group at Regeneron that invents and develops state-of-the-art tools for biologic drug discovery. We are seeking a motivated, highly organized researcher to support our investigations of new antibody and cell-based therapies. This is an opportunity for a researcher with strong molecular & cell biology skills to contribute to the development of industry-leading technologies and medicines. Responsibilities: Independently and as a team, conduct and support experiments. Investigating and develop new methodologies and technologies in molecular biology and biological therapeutics. Design, construct, and test DNA vectors, viral vectors, and cell-lines for in vitro and in vivo studies of candidate biologicals. Charact | 7/2/2019 |
| 14886 | Regeneron Basking Ridge, NJ TEMP-Clinical Study Specialist (Inflammatory & Immunology) MS Exp: 1-2 years |
The Temp - Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The Temp - CSS may be assigned to support the execution of one or more studies across a program. The Temp - CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The Temp - CSS will support internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs). They: Organizes and delivers analyzable reports and metrics to the clinical study lead. Schedules and coordinates meetings, prepares agendas, presentation materials and minutes for clinical study team meetings and other study related meetings. Collates data for assessments such as feasibility and site selection and reviews site usability database. etc. | 7/2/2019 |
| 14887 | SCA Pharmaceuticals Windsor, CT Quality Assurance Lead (3pm-11:30pm) BS in life sciences, engineering, or related Exp: 1 year in a cGMP environment |
Under the direction of the QA Manager, the Quality Assurance Lead position directs a cross-functional Quality Assurance team. The QA team supports Compounding Pharmacy Operations and is responsible for, but not limited to, batch record review, document preparation and filing and Deviation and CAPA management. This individual provides the Quality Management oversight when Compounding, Inspection, Packaging and Warehousing are in operation. Typically, the qualified person has experience managing a team of Quality Assurance personnel with a strong knowledge cGMP. etc. | 7/2/2019 |
| 14888 | Santa Cruz Biotechnology Dallas, TX Customer Service Representative BA/BS in biology or business administration Exp: Entry level |
SCBT has an immediate opening for an entry level Customer Service Representatives at its Dallas, TX Headquarters campus. This position performs telephone customer support, order processing, and data entry functions. The current shift available for this position is the early afternoon to early evenings shift, Monday through Friday. This is a full time position with career advancement opportunities within the company. Required Skills: Ability to professionally answer incoming telephones calls and effectively communicate information about products, prices, and product availability to customers. Ability to enter orders from customers in a timely and accurate manner. Ability to support the Logistics Department to ensure the timely and accurate shipment of products to customers. etc. | 7/2/2019 |
| 14889 | Santa Cruz Biotechnology Dallas, TX Technical Sales Representative, Entry Level BS in biology, chemistry, or related Exp: 1-2 years |
Santa Cruz Biotechnology, Inc. (SCBT) has immediate openings for full time Technical Sales Representatives. We have one opening for an entry level position with 1-2 years of inside sales or related work experience and one mid-level position requiring 4-8 years of inside sales or related work experience. A Technical Sales Representative is responsible for inside sales activities with customers via phone, email and live chat. The ideal candidate will actively make outgoing calls to speak to customers and build relationships with the goal of increasing sales. This is a full time position. Training on our extensive product line and related protocols is provided. etc. | 7/2/2019 |
| 14890 | Santa Cruz Biotechnology Paso Robles, CA Research Assistant BS in biology or related field Exp: Entry level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. Required Skills: Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from supervisor. Strong scientific background and business communication skills. | 7/2/2019 |
| 14891 | Santa Cruz Biotechnology Paso Robles, CA Animal Health Marketing and Sales Representative BS/MS in animal science or related Exp: Entry level |
SCAH/SCBT has an immediate opening for an entry level Animal Health Sales Representative at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. Some intermittent weekend work is required. Required Skills: Ability to work independently to achieve sales growth for the Santa Cruz Animal Health product line in the U.S. Ability to professionally receive inbound customer calls regarding orders and technical questions. Capacity to identify and source new products to broaden our product line. Ability to communicate accurate information regarding products, prices, product availability, and current promotions to customers. Ability to enter orders from customers in a timely, accurate manner. Capacity to identify and solicit new customer accounts. Ability to work as an effective team player to ensure the highest level of efficiency and success for the department and company. Excellent business communication skills (verbal, written, presentation), organizational skills and computer skills. | 7/2/2019 |
| 14892 | Santa Cruz Biotechnology Santa Cruz, CS Research Assistant BS in biology or related field Exp: Entry level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Santa Cruz, CA campus. This is a full time position with career advancement opportunities within the company. Required Skills: Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from supervisor. Strong scientific background and business communication skills. | 7/2/2019 |
| 14893 | Santa Cruz Biotechnology Sun Valley, ID Research Assistant BS in biology or related field Exp: Entry level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Ketchum, ID campus. This is a full time position with career advancement opportunities within the company. Required Skills: Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from lab supervisor. Ability to research new protocols/procedures and techniques to assist with new product development design. Excellent business communication skills. etc. | 7/2/2019 |
| 14894 | Mallickrodt Hobart, NY Manufacturing Assoc I (tableting) - 2nd shift HS Diploma/GED Exp: 0-1 years |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. | 6/29/2019 |
| 14895 | Mallickrodt Raleigh, NC Quality Tech II AS or BS in physical sciences/technical degree Exp: 1-3 years lab experience |
The Quality Tech II analyzes process samples as received and performs non-routine analysis as requested. She/he will analyze finished goods and raw materials by chemical, physical, and instrumental means to ensure quality as needed. This position will be on a rotating schedule. Performs specified analysis on all process controls samples and reports in a timely manner by telephone or computer entry using approved written procedures and proper laboratory techniques. Performs specified analysis on all finished goods using approved written procedures and proper laboratory techniques as needed. | 6/29/2019 |
| 14896 | Medicomp San Francisco, CA Cardiac Monitoring Technician HS Diploma Exp: 1+ year in healthcare |
Looking for an ECG interpreter, for our San Francisco, CA office, who is excited about having the front line responsibility of triaging the patients who have our life-saving products prescribed to them. Responsibilities include: Receiving ambulatory ECG data from phone and web transmissions. Making the correct arrhythmia call, not just knowing where to place the electrodes. Using proprietary software to efficiently compose arrhythmia reports for physicians, etc | 6/29/2019 |
| 14897 | Medicomp Burtonsville, MD Remote Holter Scanner HS Diploma Exp: 1+ year in healthcare |
I’m looking for a full time Remote Holter Scanner in the Burtonsville, MD area. Responsibilities include: Receiving ambulatory ECG data from web transmissions. Making the correct arrhythmia call, not just knowing where to place the electrodes. Using proprietary software to efficiently compose arrhythmia reports for physicians. Acquire and/or retain clinical certifications | 6/29/2019 |
| 14898 | Medicomp Burtonsville, MD Cardiac Monitoring Technician HS Diploma Exp: 1+ year in healthcare |
Looking for an ECG interpreter, for our Burtonsville, Maryland office, who is excited about having the front line responsibility of triaging the patients who have our life-saving products prescribed to them. Responsibilities include: Receiving ambulatory ECG data from phone and web transmissions. Making the correct arrhythmia call, not just knowing where to place the electrodes. Using proprietary software to efficiently compose arrhythmia reports for physician. etc. | 6/29/2019 |
| 14899 | MedImmune Gaithersburg, MD R&D Associate I/II BS or MS in chemistry or biochemistry Exp: 0-2 years |
The successful candidate will carry out analytical testing and method development using Electrophoresis, Chromatography, and Mass Spectrometry techniques in support of early and late stage development of biopharmaceutical products, such as humanized monoclonal antibodies, and recombinant proteins. The candidate will make detailed experimental observations, review and analyze data, interpret experimental results, and summarize data for presentations and reports. The candidate will author SOPs, protocols, reports and other relevant documentation. | 6/29/2019 |
| 14900 | AstraZeneca Frederick, MD Technician II - Operations BS/BA Exp: 1-3 years |
As a Production Technician II in Frederick, MD, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. It offers one of the most exciting, fast paced, challenging and rewarding work environments in the world of operations, supply chain and manufacturing. Demonstrated ability to perform all process steps of upstream / downstream / central services production operations. Ability to generate SOPs, MPRs, and SPRs for equipment and procedures used in the manufacture of biological based products. | 6/29/2019 |
| 14901 | AstraZeneca Gaithersburg, MD Pilot Production Technician I - BPD BS/BA or AA/AS Exp: AA/AS: 1-2 years, BS/BA: 0+ years |
The technician is responsible for the operation of equipment according to established Standard Operating Procedures and Master Production Records for the manufacture of therapeutic proteins and vaccines in accordance with Current Good Manufacturing Practices (cGMP’s). Operates production equipment such as bioreactors, centrifuges, filtration devices, chromatography equipment, washers, autoclaves, tanks. Weighs and checks raw materials, assembles and cleans process equipment, monitors processes. Performs SIP, CIP and manual cleaning and sanitization of equipment. etc. | 6/29/2019 |
| 14902 | MedNet Solutions Minnetonka, MN Cloud Infrastructure Engineer I BS/BA Exp: 0-3 years with Linux Admin |
Responsible for the deployment and maintenance for critical enterprise systems within a cloud Infrastructure. Serves as a technical resource for system administration of applications, operating systems, virtual machines, containers and network infrastructure. Manages and adheres to standard configuration and deployment of applications, operating systems, and network infrastructure. Investigates and analyzes system requirements and system specifications. Provides leadership and management to deliver the highest level of service to all system users. | 6/29/2019 |
| 14903 | MedPace Cincinnati, OH Entry Level Purchasing Associate AS/AA Exp: 0-1 years in business |
Responsibilities include: Create orders and purchase supplies for all Medpace entities; Maintain inventory by entering and updating item information into accounting system; Work closely with vendors to build relationships and resolve issues; Reconcile open orders on a monthly basis; Support Treasury team through new vendor setup process. | 6/29/2019 |
| 14904 | MedPace Cincinnati, OH Shipping and Receiving Associate HS Diploma/GED Exp: 1+ years in similar position |
This Warehouse Worker position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your warehouse expertise and can develop and grow your career even further, then this is the opportunity for you. | 6/29/2019 |
| 14905 | MedSpark San Luis Obispo, CA Product Development Engineer BS/BA in engineering Exp: 1+ years minimum |
Your primary role is driving conceptualization, development, and prototyping of new product concepts, focused on inventive uses of new and existing technologies that open up entirely new product concepts. Work hours and days are extremely flexible, based on need and your availability. Integrate Industrial Design Techniques to Create Designs with Improved Aesthetics, Ergonomics, and Usability. Select and Integrate Proper Materials, Components, Technologies, and Assembly/Manufacturing Processes. | 6/29/2019 |
| 14906 | LabCorp Westborough, MA Molecular Technologist BS/BA in biology, chemistry or related Exp: 1+ year lab experience |
The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, real time PCR, Sanger Sequencing and Southern Blot analysis to test for specific genetic diseases such as cystic fibrosis, spinal muscular atrophy and Fragile X syndrome to name just a few. | 6/29/2019 |
| 14907 | LabCorp Phoenix, AZ Technician AS/AA in medical lab technology Exp: 1-3 years |
Performs a variety of laboratory tests and assays in accordance with established policies, procedures and regulations in a designated technical department. Interprets results, subject to verification by Technologist/Supervisor, and providing allowance by State regulations. | 6/29/2019 |
| 14908 | LabCorp Chicago, IL Laboratory Support Technician / Data Entry HS Diploma/GED Exp: 1-3 years |
The Lab Support Technician will be responsible for performing clinical specimen accessioning, sample sorting, and data entry in a fast-paced, high-throughput environment according to established standard operating procedures. Please note, this position does not involve any actual hands on lab work. The role is primarily focused on accessioning, data entry, and supporting the laboratory. The schedule for this position will be Tuesday-Saturday, 9:30am-6:00pm. Saturday hours are 7:00am-3:30pm. Responsibilities: * Open incoming packages from clients, unpack and receive specimens * Perform data entry and Quality Assurance for specimen/patient information with a high degree of accuracy and in accordance with established protocols | 6/29/2019 |
| 14909 | LabCorp Dublin, OH Lab Assistant/Data Entry HS Diploma Exp: 0-2 years |
We are seeking a Data Entry Lab Assistant to work in our Specimen Accessioning department. The primary function of this position is to unpack and enter all data accompanying specimens received at the laboratory to begin the testing process. Candidates must possess a passion for patient care, be goal oriented, and enjoy teamwork. | 6/29/2019 |
| 14910 | LabCorp Burlington, NC Production Assembler HS Diploma/GED Exp: 0.5-1 years related work |
Perform repetitive line assembly operations to produce on-site drug test kits in accordance with Standard Operating Procedures.Make sure the proper paperwork is completed. | 6/29/2019 |
| 14911 | LabCorp Burlington, NC Specimen Processing Specialist HS Diploma Exp: 1-3 years in clinical lab |
This is a multi-discipline position with 3 primary components: specimen accessioning, sample splitting/sorting and data entry. As a Specimen Processing Specialist, your responsibilities/job duties include: Preparing laboratory specimens for designated departments/locations prior to laboratory analysis and testing and routes specimens by type to various staging areas. Performing all paperwork, technical and non-technical procedures required to process and submit specimens. Operating data entry terminals and automated data systems, follows standard sequences/coding when entering data and corrects, edits, and/or verifies data entered into automated systems | 6/29/2019 |
| 14912 | Medtronic Memphis, TN Sourcing Engineer II MS or higher Exp: 0 years |
This position has the authority and responsibility to be the primary integration point linking Strategic Sourcing with Research & Development and New Product Introduction (NPI) project teams. Technical Sourcing will lead the identification of Suppliers and reduction of overall supply risk and drive the adoption of capable technologies & sources in product development resulting in predictable supply & competitiveness through full product launch. Provides technical engineering expertise and leadership to the Supply Management organization and suppliers, serving as the technical liaison between Medtronic design requirements and suppliers' technical capability to assure that robust margins are achieved and maintained. | 6/29/2019 |
| 14913 | Medtronic Plymouth, MN Supplier Quality Engineer MS/MA in engineering, sciences, or technical field Exp: 0 years |
Responsibilities may include the following: Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Some individuals may have responsibilities that include Pre-Market Supplier Quality and duties may include: Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow Medtronic to provide customers with the highest quality and reliable products. | 6/29/2019 |
| 14914 | Medtronic North Haven, CT Quality Engineer I BS/BA in engineering, sciences, or technical field Exp: 0 years |
Responsibilities may include the following: Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. Collaborates with engineering and manufacturing functions to ensure quality standards are in place. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications. | 6/29/2019 |
| 14915 | Medtronic North Haven, CT Software Engineer BS/BA in engineering, sciences, or technical field Exp: 0 years |
You will serve as an individual contributor by providing support for the new product development and sustaining projects. The individual will assist the business in interpreting and executing against Medtronic quality system elements including software/system work products to ensure compliance. This individual will ensure that all system-level project / program work products (e.g., plans, requirements, specifications, tests, test results, traceability, risk management documents, reports) meet Medtronic’s quality, reliability, and compliance requirements. This individual will ensure Design Quality Assurance-driven initiatives meet objectives in delivering highest quality products, with supporting tools and processes. | 6/29/2019 |
| 14916 | Medtronic Louisville, CO Hardware Design Assurance Engineer I BS/BA in engineering Exp: 0 years |
Medtronic is currently seeking a Hardware Design Assurance Engineer I. Daily responsibilities include: Participate in design trade-off studies. Risk assessment. Work closely with Development Engineering to assure appropriate requirement definitions are established. Work with development engineering and manufacturing engineering to translate design requirements to manufacturing requirements. Actively participate in the product development cycle to ensure quality issues are addressed and resolved prior to release. Assist in the development and implementation of methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment. Establish incoming inspection requirements and revise as necessary. | 6/29/2019 |
| 14917 | Medtronic Miami Lakes, FL Supplier Quality Engineer I BS/BA in engineering, sciences, or technical field Exp: 0 years |
As an Associate Supplier Quality Engineer, you will be responsible for: Providing support to Operations and Receiving inspection teams in all areas of production quality assurance. Ensure components received in Miami lakes meet specifications, works with suppliers to investigate root cause and provide sound corrective actions in a fashion manner. May participate in supplier process development, supplier management, and maintaining supplier files. | 6/29/2019 |
| 14918 | Viant Ft. Wayne, IN Manufacturing Engineer I BS/BA in technical field Exp: 0-3 years |
The primary purpose of this position is to apply engineering principles to drive process improvements in the manufacturing of medical devices to positively affect Quality, Delivery, Cost, Safety and Moral. Creates and implements lean processes in a cellular environment utilizing appropriate methods such as CNC turning and milling, Wire EDM, Laser Etch, Laser and TIG welding, Polishing, Mass Finishing, Cleaning, Assembly, and Inspection. Effectively owns and manages CAPAs pertaining to their areas of responsibility. Defines, produces and implements documents including standard work and process work instructions. | 6/29/2019 |
| 14919 | Viant Ft. Wayne, IN Calibration Technician HS Diploma/GED Exp: 1+ years in calibration or related |
The primary purpose of this job is to support all calibration activities relating to the development, inspection, testing and production of product. Performs calibration, maintenance, modification, and testing on diverse types of IM&TE (Inspection, Measurement, and Test Equipment) and process control/manufacturing measuring equipment. Maintains records of all IM&TE and process control manufacturing equipment used throughout facility in compliance with FDA/ISO regulations and established procedures. Generates status reports from calibration scheduling database and works to minimize late calibrations, notifies affected areas as needed. | 6/29/2019 |
| 14920 | Viant Grand Rapids, MI Customer Service Representative HS Diploma Exp: 1+ year in customer service |
The Customer Service Representative will provide customer service and support to customers, and successfully interacts with other internal departments to resolve inquiries. The CSR processes orders in an accurate and timely manner, and facilitates internal review of capacity and materials availability. The ideal candidate will have outstanding interpersonal skills, strong organization skills, be detail oriented and possess superior problem-solving skills | 6/29/2019 |
| 14921 | Viant Grand Rapids, MI Production Operator HS Diploma/GED Exp: 1+ years work experience |
Under the director of the area Supervisor/Team Leader, the Production Operator is responsible for production work according to specifications and established policies, procedures, practices, and standards. Follow all standard operating procedures (SOPs), Good Manufacturing Practices (GMPs), and DOIs. Assemble components. Perform bar sealing/tray sealing duties. May operate packaging machine, etc. | 6/29/2019 |
| 14922 | Merck & Co Boston, MA Research Scientist, Cellular Pharmacology MS in biological sciences or related Exp: 1+ year lab experience |
The In Vitro Pharmacology department is seeking a highly motivated and technically skilled in-vitro scientist to join the Cellular Pharmacology group in Boston. The primary responsibilities will include implementation of various in vitro cellular assays, and execution of high throughput compound and biologics screens in support of internal drug discovery programs. The candidate is expected to work both independently and collaboratively with colleagues in the Pharmacology department and across other groups. | 6/29/2019 |
| 14923 | Merck & Co Durham, NC Associate Specialist, EM Sampling BS in sciences Exp: 1+ years in environmental monitoring/lab operations |
Specific to Environmental and Utility Monitoring, the Analyst will be responsible for maintaining the EM program to include the following: Collection and testing of qualified Utility systems including Clean Steam, WFI and compressed gasses. Execute environmental sampling of Classified Areas including active air sampling, surface sampling and non-viable air sampling. Provide data entry, review and approval as required. Provide summaries of test results to appropriate personnel as needed | 6/29/2019 |
| 14924 | Merck & Co Elkton, VA Operations Engineer BS/BA Exp: 1-3 years in vaccines/biologics manufacturing |
This position supports expansion of manufacturing operations in our GARDASIL® vaccine fermentation and purification production areas. The successful candidate will be a key member of a cross functional project team tasked with rapidly increasing manufacturing capacity through capital and smaller-scale improvement projects. The position will transition to supporting operations through production ramp up and into steady state manufacturing. | 6/29/2019 |
| 14925 | Merck & Co Kenilworth, NJ Scientist - Biologics Process Development MS in biological sciences/chemical engineering or related Exp: 0-3 years |
The Downstream Process Development and Engineering group within Biologics PR&D in Kenilworth, NJ to support process development for diverse therapeutic protein candidates in the Merck Research Labs pipeline. The individual will be responsible for the development of clinical and manufacturing processes for new protein candidates, focusing on both early and late stage programs with work spanning from initial process development for First in Human trials to process characterization for commercial manufacturing. In addition, the scientist will be responsible for supporting their development work with in-process analytics. | 6/29/2019 |
| 14926 | Merck & Co West Point, PA Lab Tech BS/BA in biological sciences or related Exp: 0-1 years |
Under the supervision of the Laboratory Supervisor, Senior Supervisor, Area Head or Laboratory Manager, consult with supervision concerning the planning of and perform testing on raw materials, culture media, production intermediates, manufactured bulks, finished products and/or other samples in compliance with written procedures. Testing may be performed in one or more of the following scientific disciplines: Microbiology, Biochemistry, and/or Virology. Read, record, review and calculate test results and may be required to assist in the approval/validation of test data generated according to written procedures. Assist in the revision/implementation of control procedures (CPs) and standard operating procedures (SOPs) within the department and assist in training and orientation of other Laboratory Technicians. | 6/29/2019 |
| 14927 | Merck & Co West Point, PA Scientist - Vaccine Drug Product Development MS in chemistry, biology, or engineering Exp: 0-3 years |
The successful candidate will be expected to work as part of a team that is focused on the development of vaccine drug products. The main responsibilities include the design and execution of experiments to evaluate the impact of formulation composition and the manufacturing process on yield and stability of liquid and lyophilized vaccine drug products. The successful candidate will have formulation and/or process development experience with large molecules. They should possess scientific knowledge and/or experience related to biophysical characterization, lyophilization or other drying technologies, and immunology. Effective oral and written communication skills and the ability to learn new skills quickly are essential. | 6/29/2019 |
| 14928 | Masy Bio Papperell, MA Quality Associate I HS Diploma Exp: 1+ year in ISO 9001 environemnt |
This position provides day to day support assisting in areas such as GMP, ISO 9001 and ISO 17025 compliance and the company’s quality system. Duties include quality assurance and control activities in technical, systems, operations and service areas. This position may require frequent interaction with multiple departments. Works under general supervision of management or team lead. | 6/29/2019 |
| 14929 | Lipocine Salt Lake City, UT Associate Scientist, Pharmaceutical Research and Development BS/MS in life sciences or chemical engineering Exp: 1-3 years in pharma/chem lab |
Associate scientist needed in the area of pharmaceutical drug delivery research. Responsibilities include conducting laboratory experiments in support of formulation and process development. Knowledge of laboratory practices and demonstrated skills in analytical instrumental techniques (e.g. HPLC) are preferred. Excellent communication skills needed for preparing and following standard test methods and reporting experimental results. | 6/27/2019 |
| 14930 | Liquidia Technologies Morrisville, NC Contract Manufacturing Operator AS/AA degree Exp: 0-3 years in manufacturing |
The Manufacturing Operator will support all GMP manufacturing activities by providing daily cleaning and maintenance of manufacturing cleanrooms. This position is responsible for performing and documenting routine cleaning activities and providing support for manufacturing operations. The operator will work with the Manufacturing Operations team to ensure a 1st class manufacturing organization to drive the Company’s programs to commercial success while ensuring the highest level of quality and safety standards. | 6/27/2019 |
| 14931 | Lonza Hayward, CA Manufacturing Associate I AS/BS preferred Exp: 0-2 years, Entry level |
The Manufacturing Associate Level I is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. | 6/27/2019 |
| 14932 | Lonza Portsmouth, NH Manufacturing Associate Level 1 HS diploma, AS/BS preferred Exp: 0-3 years in manufacturing |
The Manufacturing Associate Level I (Night-Shift) is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. | 6/27/2019 |
| 14933 | Lonza Walkersville, MD Process Validation Scientist I BS in biology, biochemistry, chemistry, etc. Exp: 0-4 years in process validation/development |
This individual is responsible for execution of Process Validation (PV) or for PV support with intensive supervisory direction for Liquid Media, LAL and Powder Media at the Walkersville Site. The individual performs assigned duties according to specified procedures and receives detailed instructions. The individual performs a variety of routine work within established policies and procedures, and receives detailed instructions on new projects and assignments. ble to work with intensive assistance and supervision on basic PV techniques of protocol development, execution, and reporting to ensure technical content is sufficient and accurate. This individual is expected to ask questions about content. Not approved to make protocol decisions (i.e. conclusions, product impact / validation impact assessment, and corrective actions) without review of a higher level PV scientist or Manager. | 6/27/2019 |
| 14934 | Lubrizol Corporation Wickliffe, OH Lab Technician BS/BA in sciences Exp: 1+ years lab experience |
The Lab Technician in the Blend Test Services Department is responsible for all facets of testing from the set-up and take-down to reporting of results. The majority of the workday is spent in a laboratory setting working with new and used oils, solvents, chemicals and equipment utilized to complete testing. This person is responsible for ensuring safety, quality, and timely delivery of test results while using good housekeeping practices during daily operations. Conduct quality tests following work instructions and ISO 9001 and ISO 17025 procedures. Ensure that all test protocols are in compliance with recognized industry or internal LZ test standards. Update work instructions and procedures as necessary. Plot reference data on control charts. Understand control charting and when to investigate potential issues. Must be able to identify, troubleshoot, and work closely with chemists and business partners to resolve issues or problems. Appropriately elevate the situation to chemist, manager and/or business partner when necessary. | 6/27/2019 |
| 14935 | America Regent New Albancy, OH R&D Technical Services Chemist I MS or BS in chemical engineering Exp: BS: 1-2 years in technical services, MS: 0-1 years |
Responsible for Technology Transfer and process scale up activities associated with parenteral drug products. Supports cross-functional Production, Engineering, Quality Assurance, and Validation departments to support the trouble shooting of manufacturing issues. Conduct the experiments under the supervision of Scientists for Tech Transfer, Process R&D/Scale up/Validation, and other activities needed for introduction of a new product into cGMP manufacturing site or to support process improvements of existing products. Execute laboratory experiments as per the protocols or under supervision to study material compatibility studies and/or cleaning validation activities | 6/27/2019 |
| 14936 | Lumen Bioscience Seattle , WA Lab Aid BS/BA in biology or chemistry Exp: 0-2 years, Entry level |
The position will be supporting a research biology lab actively engaged in optimizing the growth of cyanobacteria cultures. This is a full time, regular, hourly position; 40 hours per week. The work schedule is somewhat flexible, and training will be provided. Responsibilities include: Clean and maintain stocks of laboratory glassware, Maintain general laboratory solutions and other reagents, Support lab manager in maintaining stocks of consumable items, May also perform plasmid DNA purification, PCR reactions and other standard laboratory protocols | 6/27/2019 |
| 14937 | Luna Roanoke, VA Electromagnetic Research/Engineering Associate MS in electrical engineering, physics, material science or related Exp: 0-5 years |
Luna Innovations is seeking a creative Electromagnetic Research/Engineering Associate to conduct research focused on the discovery and development of new electromagnetic materials technology towards commercial applications. Current areas of development in the Advanced Materials Group include electromagnetic interference (EMI) shielding composites, coatings, and sealants; radar absorbing materials; conformal antennas; and signature control coatings. It is desired that the candidate will have a background in one or more of these areas, with specific expertise in electromagnetic material properties, EMI testing and characterization, and develop skills by contributing to program management, new idea generation, and experimental design / execution. Electromagnetic modeling and simulation experience is a plus. The candidate must be a U.S. Citizen and either have a Security Clearance or be willing and able to obtain a DoD Security Clearance. | 6/27/2019 |
| 14938 | Luna Ann Arbor, MI Application Engineer BS/BA in technical field Exp: Entry-Level |
This is an entry level position. The Applications Engineer will be responsible for testing and analysis of customer samples for feasibility and performance of our terahertz equipment. With increasing familiarity and experience with our product line the Applications Engineer may assist with customer training, field trials of the developed applications, and the installation and/or minor servicing of gauging solutions at the customer’s facility. The Application Engineer will provide remote hardware/software support to customers located within the United States. Remote and onsite services/support will include install, repair and troubleshooting of terahertz gauging software and equipment found within an industrial environment. | 6/27/2019 |
| 14939 | United Theraputics Manchester, NH Associate Biomedical Engineer BS/BA in biomedical/chemical engineering Exp: 1+ year in 3D printing |
Support and help lead 3D organ scaffold printing, helping lead both internal and external development efforts to design and formulate fluidic devices, evaluate bio-inks, evaluate biomaterial properties required for lung scaffold printing. Provide hands-on reduction to practice for manufacturing of prototypes, including the use of fluidic devices, bio-materials, non-biologic polymers, coupling and cross-linking chemistry and coatings. Establish and maintain a deep understanding of current and emerging technology in fluidics, precision machining, and biomaterials. Follow existing test practices and develop additional experimental plans to achieve project milestones; understand and adhere to critical path activities, assemble equipment necessary to execute experimental plans for prototype development | 6/27/2019 |
| 14940 | United Theraputics Research Triangle Park, NC Bioprocess Technician - Cell Biology AAS/BS/BA in biology, cmb, or biomedical sciences Exp: 1+ year lab experience |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. Routinely perform large-scale primary lung cell culture in 2D and 3D to support process development activities for a tissue engineered product. Assist with generation and maintenance of all master and working cell banks. Routinely perform bioanalytical assays to phenotypically and functionally characterize cells (such as flow cytometry and plate-based assays) | 6/27/2019 |
| 14941 | MacroGenics Rockville, MD Manufacturing Support Technician I HS Diploma or higher Exp: 6+ months experience |
The Manufacturing Support Technician I performs tasks that support and enable the manufacturing of clinical lots for MacroGenics’ multiple clinical programs. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) and produce materials necessary the next step of the manufacturing process ensuring compliance with all required specifications and regulatory requirements. | 6/27/2019 |
| 14942 | MacroGenics Rockville, MD Bioprocess Associate II – Cell Culture Sciences MS in biology, biochemistry, chemical engineering or related Exp: 0 years |
The Bioprocess Associate II is responsible for all aspects of cell culture process development, including process optimization, scale-up and characterization studies, toxicology material production, process transfer to manufacturing, and production support. This individual will also be responsible for analyzing and summarizing the data in technical reports and presentations, and troubleshooting as needed. | 6/27/2019 |
| 14943 | MacroGenics Rockville, MD QC Analyst I – Analytical BS/BA in biology, biochemistry, chemical engineering or related Exp: 0 years |
This position is responsible for performing activities to support analytical testing programs at MacroGenics to ensure compliance with cGMP standards including in-process, product release and stability testing. This individual will be required to complete the testing and related documentation in a timely manner while adhering to standard operating procedures and under cGMPs. Performs basic testing such as concentration by UV absorbance, pH, conductivity, and osmolality for in-process, product release, and stability samples on a daily basis in accordance with all protocols and procedures. Enters data into Laboratory Information Management System (LIMS). Reports out of specification results from the sampling and testing to supervisor and assists with performing laboratory investigations to determine the root cause and possible resolution. | 6/27/2019 |
| 14944 | MacroGenics Rockville, MD Manufacturing Associate II – Cell Culture AS/AA Exp: 1+ year in biopharma manufacturing |
The Manufacturing Associate II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. Operate expansion and production reactors, conduct harvest operations, and order and account for consumption of raw materials and components. Operate bioprocess equipment under strict adherence to cGMP, OSHA and required policies and regulations. Assist in the preparation and maintenance of reports and other documentation as applicable to the scope of operations in the manufacturing facility. | 6/27/2019 |
| 14945 | MacroGenics Rockville, MD Research Associate II/ Associate Scientist I (Cell Culture) MS in biology, biochemistry, or related Exp: 0 years |
This individual will work in a cell culture laboratory and be responsible for the expression of recombinant protein molecules in mammalian cells using various vectors systems and selection methods. Responsibilities include stable and transient transfections, screening and selection of stable cell lines, evaluation of cell culture conditions, biochemical assays and data analysis. This position requires working in a collaborative environment with other team members to meet MacroGenics’ objectives in research and development of therapeutic molecules. | 6/27/2019 |
| 14946 | America Regent New Albancy, OH Automation Engineer BS/BA in electrical engineering Exp: 1-3 years |
The Automation Engineer is responsible for operating and maintaining Automation/Control systems that support all Ohio facilities. The incumbent has responsibility for indirectly supervising and directing internal resources as well as contract service providers The individual will be responsible for providing Subject Matter Expertise (SME) for various Automation/Control systems including PLC’s, HMI’s, SCADA, BAS/BMS, vision systems, servo and motor controls, and associated infrastructure. | 6/27/2019 |
| 14947 | America Regent New Albancy, OH Packaging Process Automation Engineer I BS in engineering Exp: 1+ years, PLC experience preferred |
The Process Automation Engineer – Packaging I is the SME of Visual Inspection, Automatic Packaging, and serialization, working as part of the Inspection/Packaging Team for the New Albany facility. The Process Automation Engineer – Packaging I provides technical support and project leadership to all Visual Inspection related subjects for New Albany site. This position will support both commercial and Research & Development operations. The Engineer must possess the ability to manage multiple tasks simultaneously, identify and implement continuous improvement opportunities, and drive procurement and project closure in an FDA regulated environment. | 6/27/2019 |
| 14948 | America Regent Hilliard, OH Process Equipment Technician - 2nd Shift HS Diploma/GED Exp: Entry-Level |
This entry-level position is a member of the Manufacturing Team. The Manufacturing Team is responsible for activities associated with the manufacture of safe, effective and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Manufacturing Team ensure aseptic and sanitary conditions are maintained where required, that appropriate manufacturing area and equipment records are neat and accurate and that safe, effective and professional behavior is displayed at all times. In conjunction with Production Management the Manufacturing Team provides input and assistance to other Departments as needed, playing a critical role in maintaining production schedules and meeting Company goals. The Team Member will be able to participate in all aspects of the Equipment Process. | 6/27/2019 |
| 14949 | America Regent New Albancy, OH R&D Document Coordinator I BS in chemistry, pharma sciences, or related Exp: 0-1 years pharma experience |
The R&D Document Coordinator I will author, edit, review, evaluate, and maintain GMP documentation (RM documents, FP documents, Analysis SOPs, Validation Protocols, Technical reports, etc. and all required revisions). The individual will co-ordinate with Document Control and Change Request reviewers from the documents initiation to the approval stage. Draft Raw Material, In-Process, and Finished Product documents. Provide editorial support and ensure quality of all document content; focus on clarity, accuracy and consistency, while maintaining adherence to proper formats, regulatory requirements and company procedures and guidelines. | 6/27/2019 |
| 14950 | America Regent New Albancy, OH Validation Technician AS or BS in engineering, or life sciences Exp: 1+ year related experience |
The Validation Technician is responsible for validation equipment preparation, protocol execution and final report generation as directed. This position will be primarily responsible for the execution of protocols associated with the installation, operation qualification and requalification of equipment, and utilities used in the analysis and manufacture of sterile pharmaceutical drug products. | 6/27/2019 |
| 14951 | Luminex Madison, WI Reagent QC Associate BS in chemistry, biochemistry, biology, etc Exp: 1+ year lab experience |
The Reagent QC Associate assists with duties that span a broad range of activities within the quality control operations at Luminex. The selected candidate will be primarily responsible for Quality Control testing with the primary focus on raw material inspection, and in-process and final product testing. Responsibilities include: Performing assays for release of raw materials and products, and method validations . Complete appropriate documentation and data entry as required by procedures and tests performed. Reviewing and improving SOPs | 6/27/2019 |
| 14952 | Luminex Northbrook, IL Associate Scientist II MS in chemistry, biology or related Exp: 0-2 years |
The Associate Scientist II will be responsible for: Carrying out day-to-day work in the laboratory to ensure consistent performance of new products, investigate potential product or process issues, and provide supporting data for new manufacturing processes. Planning and scheduling work independently following the technical direction of scientists and senior lab personnel and following practices, procedures and protocols of the group. Participating in the design of lab experiments, write reports, procedures and other documentation, present to interdepartmental groups, general laboratory upkeep, and mentor entry level lab personnel. | 6/27/2019 |
| 14953 | Luminex Austin, TX MANUFACTURING ASSEMBLY ASSOCIATE I AS/AA in technical electropnics/mechanical field Exp: 1+ year manufacturing experience |
The Manufacturing Assembly Associate Level 1 will be responsible for : The assembly, integration of mechanical, fluidic, electronic, optical and electro-mechanical systems. System integration testing and troubleshooting for all products in of support quality manufacturing production as a typical day to day requirement. Product knowledge, documentation transfer, training and inter-departmental communication also required. Performing assigned tasks that utilize their interdisciplinary skills to perform integration troubleshooting and assigned field service tasks. Performing set-up, calibration and operation of automated and semi-automated production equipment and fixtures, based on work area. | 6/27/2019 |
| 14954 | Regeneron Rensselaer, NY eLearning Specialist MS Exp: 1-3 years |
Analyze learning needs of internal departments, design and develop digital learning solutions for those needs, and implement them through the enterprise Learning Management System or other platforms. Essential Duties and Responsibilities include, but are not limited to, the following: Project Manage and directly Design, Develop, and Implement eLearning, learning resources (wiki, websites, manuals, job aids, etc.), and digital materials for classroom trainings; including the necessary storyboards, outlines, and project plans. Apply instructional design methodologies in creation of learning solutions and assessments. Conduct training needs analysis with internal departments to gather their training requirements. etc. | 6/25/2019 |
| 14955 | Regeneron Tarrytown, NY Animal Care Technician HS Diploma Exp: 1+ years in animal care |
We are looking for a Temp Animal Care Technician. This person provides routine husbandry care and maintenance of animals, including but not limited to feeding, watering, cage changing, and health checking of animals in the vivarium as well as maintenance of the facility. The person in this role also applies technical knowledge to perform the routine care and maintenance of research animals. Responsibilities: Performs basic care of research animals for experimental purposes: daily observations to check animal health status and environment; reports changes in environment and/or animals; changes and cleans cages, equipment, water bottles and food. Unpacking and housing animals upon arrival. etc. | 6/25/2019 |
| 14956 | Regeneron Tarrytown, NY Associate Editor BA/BS Exp: 1 year |
The Associate Editor will work with more senior Medical Writing Editors and Medical Writers to learn about clinical regulatory documents and the drug development process. The individual will also work with more senior Medical Writing Editors to learn how to perform a full QC check of clinical regulatory documents, to ensure that they meet company standards and Health Authority guidelines. As the individual’s QC skills, knowledge of the drug development process and knowledge of regulatory document content increase, his/her responsibilities will increase to include more editing responsibilities (eg, checks for appropriate spelling/grammar, template use, and content). The Associate Editor will focus on learning QC techniques before learning the editing processes. etc. | 6/25/2019 |
| 14957 | Regeneron Tarrytown, NY Project Associate II (Temp) unspecified Exp: 1 year |
Supports non-drug project teams responsible for process design and improvement projects and change management within Global Development. Provides administrative and project support to EPIC & PMO team and EPIC & PMO project teams, others leaders/teams as assigned. Includes managing meeting invites and logistics, coordinating events, meetings and projects with administrative support for applications: Microsoft, SharePoint, Concur, as required, or other specialized support as required. Job Duties: Manage EPIC/PMO project workshops, events and meetings. Order and prepare session materials and AV equipement/support for EPIC events. Book rooms and order food from internal and external catering for events and meetings. etc.Supports non-drug project teams responsible for process design and improvement projects and change management within Global Development. Provides administrative and project support to EPIC & PMO team and EPIC & PMO project teams, others leaders/teams as assigned. Includes managing meeting invites and logistics, coordinating events, meetings and projects with administrative support for applications: Microsoft, SharePoint, Concur, as required, or other specialized support as required. Job Duties: Manage EPIC/PMO project workshops, events and meetings. Order and prepare session materials and AV equipement/support for EPIC events. Book rooms and order food from internal and external catering for events and meetings. etc. | 6/25/2019 |
| 14958 | Regeneron Rensselaer, NY Engineering Technician AAS in engineering technologies Exp: 0-2 years |
Works in a medical device laboratory and/or machine shop to perform testing and development activities defined by the Combination Products Applied Research group. Essential Duties and Responsibilities include, but are not limited to, the following: Maintain, troubleshoot, and repair laboratory and/or machine shop equipment. Assist with maintenance of laboratory/machine shop supplies and testing materials. Provide subject matter expertise for operation and proper application of laboratory and/or machine shop equipment. etc. Works in a medical device laboratory and/or machine shop to perform testing and development activities defined by the Combination Products Applied Research group. Essential Duties and Responsibilities include, but are not limited to, the following: Maintain, troubleshoot, and repair laboratory and/or machine shop equipment. Assist with maintenance of laboratory/machine shop supplies and testing materials. Provide subject matter expertise for operation and proper application of laboratory and/or machine shop equipment. etc. | 6/25/2019 |
| 14959 | Regeneron Rensselaer, NY Compliance Specialist Bachelor degree Exp: 0-2 years |
Essential Duties and Responsibilities include, but are not limited to, the following: Provide support, information, and assistance to individuals, groups and management with the initiation, authorship, review, submission, and followup/completion of documents such as Change Controls, EOE's, NOE's, DNF's, risk assessments, impact statements and corrective/prevention action plans. Participate/lead/author investigations and root cause analysis for department issues of non-compliance. Act as a liaison between engineering &Automation and onsite quality and regulatory groups to define and address compliance related items. etc. | 6/25/2019 |
| 14960 | RegenX Biosciences Rockville, MD Regulatory Affairs Associate, CMC BS/BA in biological sciences Exp: 1-3 years in regulatory affairs |
Reporting directly to the Senior Director of Regulatory Affairs, the Associate of Regulatory Affairs, CMC is responsible for providing support for regulatory activities related to chemistry, manufacturing, and controls for each product development area from early development through BLA. The incumbent will also provide the organization with regulatory and scientific expertise to enable high quality and effective health authority and team communications to effectively support the product development process. PRIMARY RESPONSIBILITIES: Prepare CMC-related submissions and manage regulatory writing and timely delivery of high quality technical documents including, briefing books, quality modules for clinical trial and marketing applications, drug master files, and responses to regulatory authority inquiries. Interacts with colleagues in other departments, other R&D functions and RA functions to deliver high quality dossiers, documents and materials in accordance with corporate and team goals. | 6/25/2019 |
| 14961 | Rejuvenate Bio San Diego, CA Research Assistant BS Exp: 1+ years |
Rejuvenate Bio is looking for a highly-motivated individual to join our energetic team and accelerate the development of our therapies. The research assistant position will directly support efforts to drive forward our future commercial offerings working with other RA's and scientists. The applicant will be performing standard molecular biology procedures as well as more advanced cell culture and virus creation. The role reports to senior or principal scientists at Rejuvenate Bio. Responsibilities will include: Following laboratory protocols and safety regulations. Performing standard cloning techniques (restriction enzyme, gateway, golden gate). Performing basic and advanced cell culture on a variety of cell lines. etc. | 6/25/2019 |
| 14962 | Renaissance Pharma Lakewood, NJ Associate Scientist - Formulations BS/MS in pharmaceutical sciences, chemistry, or related Exp: 1-3 years |
The Associate Scientist supports formulation development aspects of pharmaceutical products through formulation optimization to overall candidate progression for clients’ and Renaissance’s pipeline products. Applying a working knowledge of formulation science theories, practices and concepts, the incumbent works under the direct supervision of senior R&D scientists to execute, and manage product formulations projects. Insure Standard Operating Procedures and protocols are maintained and applied. Responsibilities: Under the supervision of The R&D Manager or a Senior Scientist, perform formulation and pre-formulation activities in the development and scale-up of formulations including parenteral (solutions and suspensions), and ophthalmic (solutions, suspensions and ointments) products from bench top to pilot-scale to commercial production. This may entail technology transfer from other plants as well. Conduct routine and non-routine laboratory analyses such as finished product testing, stability testing, and manufacturing in-process test which require critical levels of accuracy. etc.The Associate Scientist supports formulation development aspects of pharmaceutical products through formulation optimization to overall candidate progression for clients’ and Renaissance’s pipeline products. Applying a working knowledge of formulation science theories, practices and concepts, the incumbent works under the direct supervision of senior R&D scientists to execute, and manage product formulations projects. Insure Standard Operating Procedures and protocols are maintained and applied. Responsibilities: Under the supervision of The R&D Manager or a Senior Scientist, perform formulation and pre-formulation activities in the development and scale-up of formulations including parenteral (solutions and suspensions), and ophthalmic (solutions, suspensions and ointments) products from bench top to pilot-scale to commercial production. This may entail technology transfer from other plants as well. Conduct routine and non-routine laboratory analyses such as finished product testing, stability testing, and manufacturing in-process test which require critical levels of accuracy. etc. | 6/25/2019 |
| 14963 | ResMed Halifax, NS Inside Sales Representative BA/BS in business discipline Exp: 1-3 years |
Let’s talk about Responsibilities: Primary role is to maintain market share at current accounts by delivering exceptional service through team driven directives and assist with product training needs within the region. Develop, maintain, and grow customer relationships within assigned accounts and account managers. Develop and enhance these relationships through routine virtual customer visits, product demonstrations,educational programs, product in-services, and problem resolution. Document activities within the Customer Relationship Management (CRM) system. Work closely with the Sales Management team in evaluating business conditions and sales trends. Develop and implement a proactive plan that involves service and support with Sales Management. Let’s talk about Responsibilities: Primary role is to maintain market share at current accounts by delivering exceptional service through team driven directives and assist with product training needs within the region. Develop, maintain, and grow customer relationships within assigned accounts and account managers. Develop and enhance these relationships through routine virtual customer visits, product demonstrations,educational programs, product in-services, and problem resolution. Document activities within the Customer Relationship Management (CRM) system. Work closely with the Sales Management team in evaluating business conditions and sales trends. Develop and implement a proactive plan that involves service and support with Sales Management. | 6/25/2019 |
| 14964 | ResMed Chatsworth, CA Mold Operator, LSR HS diploma or equivalent Exp: 1-2 years |
Let’s talk about the team and you: Operates and monitors equipment/process relevant to LSR moulding by following the methods and sequence of operations as defined by verbal instructions, Visual Aids, Quality Forms and/or Routers. Let’s talk about Responsibilities: Performs to individual goals established during MyDay meetings. Operate and monitor production equipment/process – relevant to LSR. Assures product meets or exceeds company and customer expectations of quality and workmanship. Accurately reports production data. Other tasks and responsibilities as assigned. Let’s talk about the team and you: Operates and monitors equipment/process relevant to LSR moulding by following the methods and sequence of operations as defined by verbal instructions, Visual Aids, Quality Forms and/or Routers. Let’s talk about Responsibilities: Performs to individual goals established during MyDay meetings. Operate and monitor production equipment/process – relevant to LSR. Assures product meets or exceeds company and customer expectations of quality and workmanship. Accurately reports production data. Other tasks and responsibilities as assigned. | 6/25/2019 |
| 14965 | ResMed San Diego, CA Data Analyst BA/BS in business, information systems, data analytics, or related finance discipline Exp: 1+ years |
Let’s talk about the team and you: This position will be responsible for designing, building and maintaining financial reports, graphs and presentations globally at all levels of the commercial organization and will report to the Finance Manager. This will require becoming familiar with how financial data is generated and consumed across the business. Data analyst will also be involved in the expense allocation process including the creation and maintenance of allocation rules and inputs. Data analyst may also conduct research to determine the best means of obtaining and transforming data into management reports and dashboards. An ideal candidate must have significant technical proficiencies, is familiar with financial reporting and concepts, and has a passion for data. Proficiencies should include advanced excel knowledge including complex formulas, Power Pivot, and some VBA, SQL or other equivalent basic programming knowledge. Previous experience with financial and reporting systems such as Anaplan, TM1, Cognos, Oracle, Tableau or equivalent is a plus. etc. | 6/25/2019 |
| 14966 | Respironics (Philips) Nashville, TN Sales Development Specialist BA/BS Exp: Entry level (recent graduate) |
In this role, you have the opportunity to directly impact Philips’ success by qualifying leads and uncovering opportunities adding to the sales pipeline. The Campaign Management Specialist is responsible for proactive inbound and outbound prospecting and lead management; coordinating campaign strategies focusing on development, implementation and findings. This role will act as a layer between marketing and sales for all product lines including Patient Monitoring, Ultrasound and Imaging Systems. Responsible for building relationships through marketing activity – outbound call campaign, inbound inquiries, trade shows and referrals. The goal of a Campaign Management Specialist is to take a perspective lead from a campaign, generate interest to customer, qualify the lead using the budget, authority, need, & timeframe to approach and communicate the opportunity with the appropriate Account Executive for follow up. Additionally, maintaining and updating customer information in SalesForce.com and fulfilling customer request for product information. etc. | 6/25/2019 |
| 14967 | Respironics (Philips) Reedsville, PA Supplier Quality Engineer unspecified Exp: Entry level (recent graduate) |
Responsible for achieving a state of high quality performance at our Supplier partners and pursuing continuous quality improvement through the application of Quality Engineering practices on Philips products/parts/services procured from suppliers throughout the product lifecycle including sustaining change management. Responsibilities: Additions/changes/deletion to Approved Supplier List. Supplier Quality Agreement negotiation. Analysis of defects for determining if supplier caused and then notified. Supplier Quality Notifications and Supplier Corrective Action Requests (SCARs). Drive APQP Plan development, execution, monitoring and control as part of Sustaining Changes. etc. | 6/25/2019 |
| 14968 | Retrovirox San Diego, CA Marketing (entry-level part-time) unspecified Exp: Entry level |
The company is seeking an entry-level marketing person available immediately. We are seeking a fast-pace individual with experience in internet-driven social network marketing strategies with focus on use of Linkedin and Twitter to generate leads. Candidates must be located in San Diego, CA. Experience in internet-based and email-based marketing strategies is needed. Experience with website design, WordPress, email marketing and design, and SEO strategies are a plus. Ideal candidate should have some scientific background to be able to understand and implement novel strategies, evaluate competition, customer’s needs, and the services provided by the Company. Compensation will be based on commissions generated from new revenue. etc. | 6/25/2019 |
| 14969 | Revance Newark, CA Manufacturing Technician BS in biological sciences, chemical engineering, or related Exp: 0-3 years |
The incumbent will be a part of the manufacturing organization and provide hands-on execution of tasks related to the GMP manufacture of biopharmaceuticals working in Clinical and/or Commercial fill-finish. Essential Functions: Operate in clean room environment. Assist or perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.) in support of manufacturing intermediate, bulk or final drug product of acceptable quality to meet FDA regulatory quality requirements. Ensure compliance with established internal control procedure. etc. | 6/25/2019 |
| 14970 | Roche Vacaville, CA Manufacturing Technician - BioPorcess AS/BS/BA in biological or physical sciences or engineering Exp: Entry level |
As a Manufacturing Technician, you will be responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in a current Good Manufacturing Practices (cGMP) environment. You will maintain areas in a high state of inspection preparedness and will utilize business systems for inventory and process management. You will maintain records to comply with regulatory requirements utilizing cGMP and Standard Operating Procedures (SOPs) and will participate in the routine production of mammalian cell culture products within the Vacaville Manufacturing Facility, operating in at least one of the following production areas: Upstream Manufacturing (UM), Downstream Manufacturing (DM), or Production Services (PS). etc. | 6/25/2019 |
| 14971 | Rocket Pharmaceuticals unspecified, Laboratory Manager/Research Technician BS/MS in biological or health sciences Exp: 1-2 years |
Experienced and motivated lab manager and research technician to assist with daily operations of a dynamic gene therapy research lab and support development activities. The position involves managing day-to-day lab activities, including but not limited to purchase and organization of reagents and supplies, maintenance of lab equipment, and simple experimental and administrative support to a dedicated team of scientists. Responsibilities: Organize and maintain structure of the lab, managing day-to-day activities and coordinating meetings with external partners. Be responsible for shipping and receiving of materials. Participate and coordinate daily lab tasks, including maintenance of mammalian cell culture lines, and other simple lab experiments to support scientists. etc. | 6/25/2019 |
| 14972 | RTI Surgical Alachua, FL Lab Associate AS Exp: Not required for AS candidates |
POSITION SUMMARY: Conducts required biochemical or other laboratory experiments while keeping orderliness and cleanliness in the laboratory. Supports the scientific, engineering, marketing, and project management personnel in all facets of activities associated with the procurement, fabrication, processing, experimentation, and evaluation of medical products and processes. Maintaining lab equipment, maintenance, calibrations, etc. as required to sustain lab work flow/readiness. Monitors and stocks an appropriate inventory of tissue and lab supplies. Executes assigned protocols and work instructions and completes proper documentation. etc. | 6/25/2019 |
| 14973 | Regeneron Tarrytown, NY R&D Associate (Immunology/Autoimmune Diseases) BS/MS in biology, biochemistry or related Exp: 0-2 years |
We are seeking a motivated R&D associate to join the VI-Next group to support our effort in developing new in vivo disease models and testing the therapeutic potential of new candidate molecules. The new recruit will contribute to project advancement by performing in vivo work and in vitro assays such as cell culture, immunoassay and flow cytometry. The ideal candidate must have the ability to perform both in vivo and in vitro laboratory work. Strong skills in cellular and molecular biology, and knowledge of immunology are highly desirable. Involves: Immunization and injection of mice, disease and body scoring, collection and processing of blood and tissue samples. Ex vivo analysis of mouse and human samples using isolation of specific cell population techniques, primary cell culture, immunoassays such as ELISAs, ELISPOT or MSD and flow cytometry. etc. | 6/25/2019 |
| 14974 | Rockland Immunochemicals Limerick, PA Entry Level Scientist AS/BS Exp: Entry level |
We are currently seeking a reliable and ambitious team player to join our Laboratory. Our Scientists play a critical role in antibody development and supporting various teams across our organization. Important aspects of this role include excellent organizational, multi-tasking and communication skills, along with the ability to efficiently thrive in a highly interactive and goal-oriented team environment. Job Duties and Responsibilities: Performing laboratory experiments independently or with other team members as instructed. This includes, but not restricted to, buffer preparation, immunoassays creation and manufacture, material processing, column production, affinity chromatography, inventory management and product handling. Maintain laboratory space, equipment and inventory in an appropriate and professional manner. Excellent attention to detail, proactive planning and ability to organize and carry out tasks with quality in a timely fashion. etc. | 6/25/2019 |
| 14975 | RepliGen Marlborough, MA Membrane Manufacturing Engineer BS in chemistry or chemical engineering Exp: 1-3 years |
As an expert in single use tangential flow filtration, Repligen offers TangenX® Flat Sheet TFF Cassettes with unparalleled flexibility and scalability from process development to production scale. Since 2008, SIUS tangential flow filtration products have been universally accepted as the first purpose built single use tangential flow filtration cassette ideally suited for downstream purification operations. The individual will work in the manufacturing of novel high performance ultrafiltration and microfiltration membranes – with an ultimate goal of impacting bioprocessing biological molecules. The work will also include improvements in membrane formation processes. The work will require a good understanding of polymers and membrane formation processes. We are seeking a Membrane Engineer within the operations group to focus on the manufacturing of existing and new ultrafiltration membranes. etc. | 6/25/2019 |
| 14976 | RepliGen Rancho Dominguez, CA Assembler I HS Diploma/GED Exp: 0-1 years |
This assembly position performs a wide variety of fiber assembly, filtration product assembly or sub-assemblies. Determines and/or follows methods and sequence of operations in performing fiber bundling, filter potting, filter welding, fitting on assembly units and packaging. The employee also works as a team member in whatever capacity and job function is required to deliver a quality product to our customer in a timely fashion. Performs manual assembly of complex fiber, membrane, and polycarbonate components, etc. | 6/25/2019 |
| 14977 | RepliGen Rancho Dominguez, CA Material Handler HS Diploma Exp: 1-2 years |
Under general supervision. Organizes and transports production and support material and equipment within the area of assignment. May use manual and powered material handling equipment and packaging equipment. The skills, efforts, responsibilities and working conditions are outlined below and made part of this description. Job Functions: Locate, pick, move and store material and equipment according to established procedures, both written and verbal. Unloads and stores material in proper locations and perform receiving transactions. Use material handling equipment such as hand and powered pallet movers, fork trucks and some powered packing equipment such as banders and shrink wrappers. etc. | 6/25/2019 |
| 14978 | Quanterix Billerica, MA Receptionist HS Disploma/AS/AA Exp: 1-3 years in customer facing profession preferred |
Description of Job Responsibilities: Provide front desk telephone/reception coverage and general administrative support. Answer incoming calls, screen and forward to appropriate individuals, or take a message. Answer general inquiries. Greet Quanterix guests, direct or escort them to the appropriate individual. Upkeep of visitor sign-in/log. Schedule appointments and maintain/update calendars as needed. Update/maintain visitor signage board. Schedule and maintain customer conference rooms. Receive, sort and deliver daily mail. Assist customers in booking hotel reservations. May also assist with some travel planning. Maintain a “Visitor Guide” local hotels, restaurants, etc. etc. | 6/24/2019 |
| 14979 | Quotient Sciences Boothwyn, PA Analytical Scientist II MS Exp: 0-2 years |
The position may reside in any one of the functional areas and carry out the responsibility under some supervision: Operate and troubleshoot the following instruments/equipment to test pharmaceutical samples: HPLC/UPLC, Dissolution apparatus, Karl-Fisher water content titrator, GC, FTIR, UV, Other analytical instruments as directed. Follow analytical test methods, compendial methods, experimental procedures and SOP’s. Document test results in laboratory notebook, in real-time, and communicate status of test results to supervisor. Peer review of laboratory notebooks for technical details. Maintain control of all project related samples submitted to the laboratory. etc. | 6/24/2019 |
| 14980 | Quotient Sciences Garnet Valley, PA Staff Formulator MS Exp: Not required for MS candidates |
The Role: Develop stable and bioavailable pharmaceutical dosage forms. Develop and optimize manufacturing processes and manufacture clinical supplies. Responsible for developing formulations and manufacturing process for pharmaceutical dosage forms to meet customer needs. Perform pre-formulation, formulation, manufacturing process development/optimization for various batch sizes (lab to production scale), and equipment and process validation under strict cGMP guidelines. Prepare and review SOPs, batch records, protocols, development reports. Prepare and monitor stability protocols per ICH guidelines. Evaluate stability results of formulation prototypes and clinical supplies. Evaluate packaging components. etc. | 6/24/2019 |
| 14981 | Radius Health Waltham, MA Quality Assurance Coordinator BS Exp: 1-3 years |
The QA Coordinator plays an essential role in the management of key GXP (Good Clinical / Manufacturing / Laboratory / Pharmacovigilance / Distribution Practices) Quality Assurance records and documents, including training curriculum management and assignment and Quality Management System records such as deviations, investigations, Audits, Audit Findings, Corrective and Preventative Actions (CAPAs), vendor qualifications and inspections. Responsibilities: Maintains training requirements matrix, tracking role-based training requirements across the company. Assigns training to new and current employees according to the training matrix. Tracks and generates compliance metrics on training completion. etc. | 6/24/2019 |
| 14982 | Radius Health Wayne, PA Human Resources Coordinator BA/BS in HR, business administration, or related Exp: 1+ years in an HR position |
The HR Coordinator is a central position for the HR Function at Radius. The role will complete administrative duties to support the HR function as well as the Wayne, PA office and coordinate some activities virtually as needed for the Waltham, MA office. The role requires excellent organizational and communication skills as well as the ability to problem solve and proactively diagnose/ address issues and concerns. Responsibilities: Maintain all office needs; welcome visitors, manage office supply orders, maintain office environment, handle main phones. Primary contact on HR Connect a centralized HR service (email, phone) for all employees and external candidates. Involves timely responses, researching and diagnosing employee inquiries, running back office HR process, etc. etc. | 6/24/2019 |
| 14983 | Reckitt Benckiser Parsippany, NJ Supply Graduate Development Program BS in supply chain, engineering, or business related field Exp: Entry level |
We are looking for graduating students to join our RB Supply Graduate Development Program. The program includes rotations that allow you to gain a holistic view and exposure to the entire Supply Chain function. During the rotations, you’ll be gaining valuable experience and building on functional fundamentals, as you get your feet wet with responsibilities supporting each respective function. Rotations also allow you to work in various locations throughout RB’s US offices, adding to the breadth of exposure needed to become a true success at RB! A brief description of each function is found below: Customer Service – RB’s key player in managing flow of orders and determines team ability to add value to local business. Planning (Custom Manufacturing, Demand Planning, S&OP) - Control tower of Supply Services. Serve as point of contact between RB Commercial and RB Manufacturing. Logistics (Transportation, Warehousing, Corporate Logistics) – This is where “the rubber hits the road” in terms of managing not only the key operational aspect of the Supply Services team but also the most significant costs within Supply Services. Manufacturing - Takes place in each factory; where raw and packaging materials are transformed into packaged ready products. etc. | 6/24/2019 |
| 14984 | Reckitt Benckiser Parsippany, NJ IS Graduate Program BS in business or information science related field Exp: Entry level (graduating May/June 2019) |
We are looking for graduating students to join our RB IS Graduate Development Program. You will be completing IS based project work, collaborating with multiple functions such as Supply Finance, Commercial Finance, and Accounting. Responsibilities: Develop a basic understanding of each function, specifically around the organizational structure, operational processes, common issues and pain points. Perform system analysis, design, programming, testing, and documentation. Monitor and analyze existing application systems. Recommend enhancements on technical function and business utility. Constantly improve IS systems through current/best in class IS practices. etc. | 6/24/2019 |
| 14985 | Reckitt Benckiser Parsippany, NJ Finance Graduate Development Program BS in accounting or finance Exp: Entry level (graduating 2019) |
We are looking for graduating students to join our RB Finance Graduate Development Program. You may do rotations through: Supply Finance, Commercial Finance and Accounting. Responsibilities: Collect, process, verify, and report accounting related information. Perform professional analytical and management to support work assignments. Assist in preparing monthly financial reports, developing and/or utilizing spreadsheets, databases and other computer applications. Process specialized information, reports, and forms for fees, billing, project tracking, etc. Enter information reports into a financial accounting system. etc. | 6/24/2019 |
| 14986 | Reckitt Benckiser Parsippany, NJ Assistant Brand Manager MBA Exp: Entry level (graduating spring 2019) |
We are looking for an MBA student to join our brand management team as an Assistant Brand Manager. This position is responsible for the development of assigned brands through the achievement of specific growth objectives. The position resides within the US Marketing function and will assume support for the Brand Manager for assigned brands within the category in Equity, Activation or Innovation capacities. The Assistant Brand Manager will play a key role in supporting the development of the overall category strategy, and is expected to drive the growth of his/her assigned brands through excellent marketing execution. Responsibilities: Support in developing and delivering the vision, US in-market activation excellence and gross profit for the brand. Champion pipeline and secure incremental funding for launches. Manage the day-to-day interface and key business activities of the portfolio. etc. | 6/24/2019 |
| 14987 | Reckitt Benckiser Parsippany, NJ Performance Marketing Analyst BA/BS Exp: 1+ years in media industry |
A fantastic opportunity is available for a Performance Marketing Analyst to join our Marketing team in Parsippany, NJ: Activation practitioner with experience in the media/search marketplace, who is eager to have immediate impact on RB E-Business team in its activation and optimization practice. Energized by the development of data architectures to drive performance along with executing dashboards that drive clear analysis and insights on in-market media results. Eager to create meaningful vendor partnerships & act as daily trader within self-service media platforms. ‘Hands on Keyboard’ operational activation & management of e-commerce Search/SEM strategy with stewardship of keyword, bid and pacing management Maintain relationships across Amazon AMS, AMG & Criteo Stewardship of go-to-market marketing approach across Bricks & Clicks customers, inclusive of activation of display & SEM campaigns. | 6/24/2019 |
| 14988 | Reckitt Benckiser Montvale, NJ R&D Microbiology Lab Technician AS Exp: 1-2 years |
The R&D Technician will apply technical knowledge working toward multiple project goals and objectives within established timelines. Perform laboratory tasks using general microbiological laboratory techniques. Perform appropriate practices and procedures in line with standard operating procedures. Maintain laboratory records in compliance with Good Laboratory Practice standards. Prepare microbiological media, reagents, glassware, and process contaminated materials. Read and interpret microbiological test results. Maintain an adequate inventory of laboratory supplies. etc. | 6/24/2019 |
| 14989 | Reckitt Benckiser Atlanta, GA Independent Pharmacy Sales Representative BA/BS Exp: 1-2 years in business sales |
The Independent Pharmacy Sales Representative (IPS) is responsible for achieving sales goals and implementing company approved programs within an assigned geographically defined territory. Sales & Merchandising responsibilities include driving front end execution for RB brands. This includes driving incremental SKU distribution, display sales as well as sustaining product distribution, shelving and promotion activities for RB branded products. Duties include successful sales of conceptual products and programs to store level decision-makers while maintaining trusting relationships. Excellent selling and negotiation skills will allow you to provide compelling reasons to purchase, or display, against the competition. etc. | 6/24/2019 |
| 14990 | Reflexion Hayward, CA Firmware Engineer MS in electrical or computer engineering Exp: 1+ years |
The Firmware Engineer at RefleXion will have firmware responsibility for the RefleXion‘s embedded system. This engineer is expected to deliver firmware solutions for interfacing hardware resources to application programs. The engineer will work with a highly integrated team on specification, design, debug, verification and validation, CE approval, FDA submissions, and documentation control. The successful candidate will be a strong technical contributor with a deep grounding in sound firmware development practices in an embedded systems environment. In addition to expertise in firmware development, the engineer will be expected to understand medical device quality systems and design control, including specification, hardware and firmware risk analysis, and formal testing. He or she will engage on any and every issue necessary to ship products to customers of the highest quality and reliability. etc. | 6/24/2019 |
| 14991 | Rakuten Medical San Mateo, CA Clinical Trial Associate BA/BS in relevant scientific field Exp: 0-1 years |
This position will be responsible for providing project management support to all ongoing clinical trials and development programs within Global Clinical Operations. The position will work closely with leadership team in developing, actively managing, and ensuring delivery across all aspects of planning and execution of product development at the clinical stage, as well as supporting other functional areas throughout the product life cycle from pre-clinical to commercial. The successful candidate must thrive in a fast‑paced team environment, and have excellent communication, planning, and organizational skills. We welcome innovative and highly motivated individuals who can bring ideas to life through collaboration, communication, and execution. Key Duties and Responsibilities: Support the team in ensuring that quality clinical trials are conducted per protocol, in a timely fashion, and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals and established study budgets. Support the study team with start-up activities, enrollment, site management, data collection, data reviews, site feasibility, database lock, etc. Provide logistical support for Clinical Trial Managers and study team. etc. This position will be responsible for providing project management support to all ongoing clinical trials and development programs within Global Clinical Operations. The position will work closely with leadership team in developing, actively managing, and ensuring delivery across all aspects of planning and execution of product development at the clinical stage, as well as supporting other functional areas throughout the product life cycle from pre-clinical to commercial. The successful candidate must thrive in a fast‑paced team environment, and have excellent communication, planning, and organizational skills. We welcome innovative and highly motivated individuals who can bring ideas to life through collaboration, communication, and execution. Key Duties and Responsibilities: Support the team in ensuring that quality clinical trials are conducted per protocol, in a timely fashion, and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals and established study budgets. Support the study team with start-up activities, enrollment, site management, data collection, data reviews, site feasibility, database lock, etc. Provide logistical support for Clinical Trial Managers and study team. etc. This position will be responsible for | 6/24/2019 |
| 14992 | Rakuten Medical San Diego, CA Laboratory Technician & Receiving Clerk AS/BS in a biological or chemical field Exp: College level laboratory experience |
This person will be responsible for the general care and upkeep of the laboratory. This includes preparation of reagents/solutions, cleaning of incubators, BSCs and other lab equipment, regular cleaning and disinfection of lab surfaces necessary to maintain the safety of the physical environment and the organization/restocking of lab supplies. Key Duties and Responsibilities: Clean and sterilize laboratory equipment used in tissue culture. Prepare reagents and solutions. Maintain chemical inventory and SDS notebook. Maintain supply levels in laboratory and note items needed. | 6/24/2019 |
| 14993 | Rakuten Medical San Diego, CA Senior/Associate - Technical Operations (Molecular Biology) MS Exp: 0-3 years |
Key Duties and Responsibilities: Conducting primer design, PCR, gel electrophoresis, Quikchange mutagenesis, restriction enzyme digestion/analysis, ligation, sequence and ligation independent cloning. Responsible for cloning constructs (antibody, therapeutic proteins, or research reagents) and purifying DNA at different production scales (Mini-, Midi-, Maxi-, Giga-) to support critical reagents needs, material generation efforts, and cell-line development activities. Responsible for ordering and maintaining raw materials, lab supplies, and providing oversight to inventory of all required working reagents. Maintain, calibrate, and troubleshoot molecular biology-related equipment. Document experimental procedures, quality control, stocking and tracking reagent inventory. Responsible for working with DNA analysis software programs such as DNAStar, Vector-NTI or equivalent. etc. | 6/24/2019 |
| 14994 | Keystone Nano State College, PA Research Chemist MS in biochemistry/chemical engineering Exp: 0-2 years |
Essential job duties include: Assist in designing experiments to develop and manufacture custom specialty products. Set up and conduct chemical experiments, tests, and analyses using techniques such as spectroscopy, chromatography, physical and chemical extractions, dynamic and quasi-electric light scattering and microscopy. Compile and interpret results of tests and analyses Prepare graphs and charts to document experimental results for presentation to management. | 6/23/2019 |
| 14995 | Kiniksa Lexington, MA Temporary Process Dev. Lab Specialist, Internal Dev. & Mfg. BS Exp: 0-2 years in biotech |
The individual will support buffer/media production in process development and pilot scale clinical manufacturing for products within the Kiniksa pipeline. In addition, the individual will support upstream/downstream operations in the manufacturing and process development department. This individual will also periodically support other disciplines including shipping, receiving and purchasing. It is preferred, but not required, that the candidate have experience with disposable technologies and solution preparation. The candidate must be highly motivated, eager to learn, science driven, and results oriented in a team environment. | 6/23/2019 |
| 14996 | Elbit Systems of America Merrimack, NH Data Analyst BS/BA Exp: 0-2 years |
The position will support data coordination and analysis as requested and prioritized by management. Revises, analyzes and maintains data reports and conducts analysis. Prepares management and statistical summaries and reports to assist upper management in decision-making and improvement. Assists in determining means to obtain appropriate data and ensures accuracy and integrity of the data. Assists in analysis and implementation of current processes. | 6/23/2019 |
| 14997 | KSQ Therapeutics Cambridge, MA Associate Scientist - Target Discovery BS or MS in biology/immunology or related Exp: 1-2 years lab experience |
The successful applicant will use their cell and molecular biology understanding to support the development of autologous T cell transfer therapies. Responsibilities include: Perform supervisor-guided cell and molecular biology experiments in the lab. Contribute to the development and characterization of genetically engineered cancer cell lines, and primary immune cells. Support process development efforts for KSQ’s autologous T cell transfer therapy programs. Document, and communicate experimental design and data | 6/23/2019 |
| 14998 | KVK Tech Newtown, PA Topical Formulation Associate MS in bio/chemistry, pharma sciences, or related Exp: 1-3 years |
Responsibilities include: Assist in the development of broad range of topical product pharmaceutical formulations including gels, creams, solutions and ointments. Develop pharmaceutical formulations utilizing Quality by Design (QbD) and risk assessment concepts. Contribute and support the analytical efforts and interpretation of data generated from experimental batches. Write technical documents to support regulatory submissions and technical transfers. | 6/23/2019 |
| 14999 | KVK Tech Newtown, PA QC Document Reviewer BS/BA in chemistry or related Exp: 1+ year in GMP lab |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards | 6/23/2019 |
| 15000 | KVK Tech Newtown, PA Quality Control Microbiologist BS/BA in microbiology or related Exp: 0-1 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensure their delivery in an accurate and timely manner following proper safety precautions. Also provide QC microbiology support to the Aseptic Manufacturing and validation process. Performs Microbiological Tests and studies by following the established procedures referenced in the official sources. Preparation of microbiological media and diluents by following laboratory procedures, etc. | 6/23/2019 |
| 15001 | KVK Tech Newtown, PA Manufacturing Operator HS Diploma or higher Exp: 1-3 years in operation |
Operators are responsible for operating special purpose machines or industrial equipment to specifications on production basis in typical oral solid dose pharmaceutical manufacturing. Processes include dispensing and weighing of materials, using automatic and semi-automatic equipment for tablet manufacturing, combining materials to make blends and solutions, and packaging of finished product. | 6/23/2019 |
| 15002 | KVK Tech Newtown, PA Sample Management Associate BS/BA Exp: 0 years |
Sample Management Associate provides support to Sample Coordinator and performs administrative tasks in the Sample Management Department. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. Performs duties and training to acquire the skills required for sample and standard handling in support of the laboratory. Quality Control related taskslike receiving, documenting, distributing and reconciliation of all samples received in the laboratory. | 6/23/2019 |
| 15003 | LabCorp Birmingham, AL Lab Assistant HS Diploma Exp: 1-2 years |
Responsibilities include: Performs all paperwork, technical, and non-technical procedures required to process and submit specimens. Assigns specific computer generated identification numbers, checks for accuracy, and records all items processed. Forwards accessioned specimens to designated laboratory location(s); and locating and correcting any discrepancies. Learns and keeps familiar with lab procedures and location of stored specimens. | 6/23/2019 |
| 15004 | LabCorp Saint Paul, MN Clinical Lab Assistant HS Diploma Exp: 0-1 years |
Responsibilities as a clinical lab assistant include: Prepare laboratory specimens (blood and body fluids) for testing. Mixing of chemicals in preparation for laboratory processing. Prepare and scan documents. Maintain a clean, well-stocked, organized work area. Follow all Standard Operating Procedures including safety and quality standards | 6/23/2019 |
| 15005 | LabCorp Phoenix, AZ Specimen Processor HS Diploma Exp: 0-2 years |
Job Duties/Responsibilities: Prepare laboratory specimens for analysis and testing. Unpack and route specimens to their respective staging areas. Accurately Identify and label specimens. Pack and ship specimens to proper testing facilities. Meet department activity and production goals. | 6/23/2019 |
| 15006 | LabCorp Bloomington, MN Phlebotomist - Float HS Diploma Exp: 0-2 years |
Job Duties/Responsibilities: Perform blood collections by venipuncture and capillary techniques for all age groups. Collect specimens for drug screens, paternity tests, alcohol tests etc. Perform data entry of patient information in an accurate and timely manner. Process billing information and collect payments when required. Prepare all collected specimens for testing and analysis. | 6/23/2019 |
| 15007 | Lantheus Medical Imaging North Billerica, MA Manufacturing Technician II AS in sciences Exp: 1-2 years in pharma/biotech |
The objective of this position is to perform operations within the Finishing Operations Team to support the manufacture of radioactive products in a timely and compliant manner based on business needs. Incumbent ensures that the integrity and quality of the products produced comply with the associated operating procedures to meet all cGMP, regulatory, and safety requirements. This position may require mandatory overtime, as needed, supporting finishing operations on holidays, weekends, and/or late and early production shifts. | 6/23/2019 |
| 15008 | Lantheus Medical Imaging North Billerica, MA Cleaning Technician HS Diploma Exp: 1-3 years |
Perform cleaning and disinfection services within controlled environment manufacturing areas (i.e. clean rooms) to ensure compliance with current Good Manufacturing Practices (cGMP) and US Food and Drug Administration (US FDA). Maintain the assigned area housekeeping (per cGMP compliance) such as: cleaning walls, floors, doors, drains, windows, and other general surface areas. Follow written standard operating procedures to fulfill cGMP requirements for cleaning and disinfection of controlled clean room environments. Properly document completion of facility cleaning/disinfection in the form as required per SOP. Maintain cleaning equipment in good working condition, maintain cleaning/disinfection inventory, and keep cleaning supplies and equipment storage areas in neat and safe order. | 6/23/2019 |
| 15009 | Latitude Pharma San Diego, CA Research Associate-Analytical Development BS in chemistry, pharma or biochemistry Exp: 1-5 years in lab setting |
LATITUDE is seeking a Research Associate to carry out individual drug formulation development projects for our clients. LATITUDE utilizes its extensive experience and proprietary technologies to solve issues of insolubility, instability, poor absorption and other formulation challenges over a range of dosage forms for both external clients and internal programs. A successful candidate will possess proficiency in a variety of analytical chemistry techniques including HPLC. This is a salaried, full-time position at our San Diego location. | 6/23/2019 |
| 15010 | LifeMine Cambridge, MA Research Associate, Biochemistry & Biophysics MS in biology, bio/chemistry, or related Exp: 1+ years |
LifeMine is seeking a motivated Research Associate to be an integral member of the Biochemistry team responsible for discovering and developing fungal derived drugs to targets of exceptional therapeutic value. Responsibilities include: Perform enzymatic and protein-protein interaction assays for multiple targets. Execute routine screening assays. Present results at group and/or project meetings. Maintain and track an inventory of biochemical reagents. | 6/23/2019 |
| 15011 | Ligand San Diego, CA Corporate Development Associate BS in finance, accounting or sciences Exp: 1-3 years in investment, management, or finance |
The Corporate Development Associate reports to the Senior Director, Corporate Development and Investor Relations and supports all aspects of Ligand’s corporate development (M&A) and general strategy functions with significant exposure to senior corporate leadership. Responsibilities include: mergers & acquisitions (Perform financial valuation and other qualitative analysis on target acquisition candidates, Assist and creation of presentation materials for senior management and Board of Directors review, Monitor market conditions, evaluate companies and/or assets and maintain potential deal list, etc.) | 6/23/2019 |
| 15012 | Leidos Madison, AL Engineering Tech I BS/BA Exp: 0-2 years |
Leidos is seeking an Engineering Tech 1 to manage the test environment for the NASA NEST contract. The Test Engineer provides Entry-level test engineering support. Applies fundamental concepts, processes, practices and procedures on technical assignments. Evaluates, recommends, and implements automated test tools and strategies. Develops, maintains, and upgrades automated test scripts and architectures for application products. | 6/23/2019 |
| 15013 | Lifecore Chaska, MN Regulatory Affairs and Product Support Associate BS/BA in life sciences or engineering Exp: 1+ years in FDA regulated industry |
The Regulatory Affairs and Product Support Associate will proactively support, along with other members of the organization, projects and regulatory submissions for Lifecore customers and their products. They will assist with or lead preparation and maintenance of required regulatory submissions, such as Drug Master Files (DMF), Device Master Files (MAF), design dossiers, change notifications, technical files, etc.; assist with maintenance of Master File database; provide regulatory support to Lifecore customers as necessary; assist or lead complaint handling and MDR/vigilance activities; review and approve change orders and CATSweb actions; review internal change requests to ensure regulatory compliance and good quality assurance practices; assist in compiling, formatting and maintaining documentation for domestic and international product registrations, including making copies and filing; participate in FDA, ISO and Client Audits. | 6/23/2019 |
| 15014 | Lifecore Chaska, MN Machine Operator I HS Diploma Exp: 6+ months |
The Machine Operator I is responsible for the setup and operation of standard packaging machinery in the packaging department. This includes working with and monitoring other packaging personnel to complete equipment set up and operation required by the department schedule. Machine Operators must comply with regulatory requirements, Good Manufacturing Practices (GMP), Standard Operating Procedures (SOP), and Manufacturing Process Records (MPR). They will perform all processes as required to fill, label, print, tray seal, pouch, final package, and inspect any Lifecore product; document completed work during packaging of final product; continually practice proper precautions and procedures when working with equipment and handling chemicals; participate in the review of batch records, etc. | 6/23/2019 |
| 15015 | LifeSensors Malvern, PA Entry Level Scientist BS or MS in biological sciences Exp: 0-2 years lab experience |
Successful candidates will have basic knowledge of biochemistry and molecular biology techniques, in particular experience with, protein expression andpurification and cloning. Knowledge of the ubiquitin proteasome pathwayis desired. | 6/23/2019 |
| 15016 | LakePharma Hopkinton, MA QC Analyst 1 BS/BA Exp: 0.5-2 years |
Responsibilities include but are not limited to: Routine work in a BSC. Working knowledge and use of micropipettes. Exposure to HPLC a plus. Exposure to IEF. Familiar with SDS page. Etc. | 6/23/2019 |
| 15017 | LakePharma Belmont, CA Operations Assistant/ Operations Associate I AS or BS in business Exp: 1-2 years |
Responsibilities include but are not limited to: Greet all employees, visitors and guests and ensure they have a great experience. Answer and route incoming calls. Clerical duties such as scanning, digital filing, and data entry and report generation. Operations, shipping and receiving responsibilities including QC packages coming and going to ensure clients receive the correct items according to our protocols. | 6/23/2019 |
| 15018 | Katalyst Barrington, IL Chemistry Lab Technician/Client: Pepsi BS in chemistry/biochemistry Exp: 0-3 years lab experience |
Duties include: Process submitted samples into forms ready for analysis, such as grinding solid samples to a homogeneous mixture. Perform routine laboratory chemical analyses and/or instrumental test procedures using standard methods of analysis, and then calculate and report the assay results. Prepare and maintain chemicals, chemical solutions, sample dilutions, and equipment as needed for the performance of analyses. Maintain accurate records and documentation and assure the reliability of measurement systems by using appropriate GLP. | 6/22/2019 |
| 15019 | KBI BioPharma Durham, NC Process Development Associate MS in biochemistry/chemical engineering Exp: 0+ years |
This is a position in the Downstream Process Development group involving the planning and execution of purification pilot/scale up and lab-scale confirmation runs for biological therapeutics using chromatography, precipitation, and filtration methods. Duties include: Use of AKTA chromatography systems with Unicorn 7 software. Use of pumps for normal and tangential flow filtration operations. Use of pH and conductivity meters. Assist in the evaluation, development and implementation of new downstream. technologies leading to process improvements and efficiency of operation. etc. | 6/22/2019 |
| 15020 | KBI BioPharma Durham, NC Process Development Associate MS in biochemistry/chemical engineering Exp: 0+ years |
This is a position in the Downstream Process Development group involving the planning and execution of purification pilot/scale up and lab-scale confirmation runs for biological therapeutics using chromatography, precipitation, and filtration methods. Duties include: Use of AKTA chromatography systems with Unicorn 7 software. Use of pumps for normal and tangential flow filtration operations. Use of pH and conductivity meters. Assist in the evaluation, development and implementation of new downstream. technologies leading to process improvements and efficiency of operation. etc. | 6/22/2019 |
| 15021 | KBI BioPharma Durham, NC Quality Systems Specialist I BS in pharma, biology, chemistry, or related Exp: 1-2 years in computer support/admin/pharma industry |
Responsible for quality computer system administration, providing technical/end user support for quality computer system, and maintaining close communication with management to keep stakeholders apprised of quality computer system incidents/ resolutions, project validation status, and other relevant issues. The role requires leading and/or assisting in quality computer system validation efforts and ensuring all work is carried out in compliance with cGMPs, company policies and procedures, 21 CFR Part 11, EU Annex 11, ICH guidelines, and other applicable industry regulations. | 6/22/2019 |
| 15022 | KBI BioPharma Durham, NC In-Process Support Associate BS in sciences Exp: 0-2 years in QC |
We are seeking an In-Process Support Associate with strong protein chemistry background to perform cGMP in-process analytical support. These services include in-process and release testing for drug substances manufactured internally. Responsibilities include: Execute activities according to cGMP regulations and company SOPs. Provide STAT assay coverage including 2nd shift and weekends as required by the manufacturing schedule. Assays include A280 and RP titer. Log samples or verify sample log in outside of standard business hours. etc. | 6/22/2019 |
| 15023 | KBI BioPharma Durham, NC Data Reviewer/Research Associate MS in biochemistry/chemical engineering Exp: 0+ years |
Perform data review for contract services projects, including analytical and formulations programs for monoclonal antibodies, recombinant proteins, peptides, and small molecules in a variety of dosage form such as liquids and lyophilized powders and suspensions for injection, topical gels, and other novel delivery systems. Perform timely review of cGMP data from HPLC, ELISA, CE, etc. with a high focus on data quality and integrity to ensure accuracy, completeness, and compliance. | 6/22/2019 |
| 15024 | KBI BioPharma Durham, NC Microbiology Associate BS in sciences Exp: 0+ years |
Perform daily environmental monitoring and assist in collection and transfer of samples for laboratory analysis. Perform microbiological in-process and release testing in support of GMP manufacturing. Tests include, but are not limited to: bioburden, microbial purity and endotoxin. Execute environmental monitoring (EM) within all classified manufacturing areas according to approved SOP’s and cGMP’s. Provide EM support for manufacturing during specified dynamic conditions. | 6/22/2019 |
| 15025 | KBI BioPharma Durham, NC Research Associate-Analytical Development BS/MS in chemistry/biochemistry or related Exp: 0+ years |
Responsible for executing and managing method transfer, method development, and/or qualification of test methods to be used for process characterization testing. Responsible for executing assays in support of process characterization studies. Responsible performing elementary data analysis and reporting of results to corresponding internal departments. Familiar with protein characterization technologies such as: HPLC, ELISA, and UV-Vis. Familiarity with automated analysis technologies such as TECAN, BioTek, or similar automated liquid handling platforms.Responsible for executing and managing method transfer, method development, and/or qualification of test methods to be used for process characterization testing. Responsible for executing assays in support of process characterization studies. Responsible performing elementary data analysis and reporting of results to corresponding internal departments. Familiar with protein characterization technologies such as: HPLC, ELISA, and UV-Vis. Familiarity with automated analysis technologies such as TECAN, BioTek, or similar automated liquid handling platforms. | 6/22/2019 |
| 15026 | KCAS Shawnee, KS Analyst I, Biopharma LBA BS/BA in sciences Exp: 1+ years lab experience |
The Analyst I is responsible for preparation of reagents and solutions, as well as sample processing under required regulatory documentation. May also analyze data, interpret results or contribute to troubleshooting activities. Conducts sample inventory and carries out lab support duties as assigned, such as inventory of chemicals, washing glassware, waste disposal and/or general cleanup. | 6/22/2019 |
| 15027 | Invitae Cambridge, MA Bioinformatics Engineer, Algorithm BS/BA or equivalient work in bioinformatics Exp: 1+ year in similar role |
As part of the pipeline engineering team, you will be responsible for maintaining, improving, and adding to our catalog of production bioinformatics pipelines across an expanding set of modern assays. You will be responsible for scaling our pipelines as we work toward our goal of providing low-cost genetic answers to billions of people. You will work and learn among an extraordinary set of peers: bioinformaticians, molecular biologists, and software engineers. Your work will directly improve the quality of our product and positively impact each tested patient. | 6/21/2019 |
| 15028 | Invitae San Francisco, CA Histologist BS or MS in biological sciences, HT-ASCP or HTL_ASCP Exp: 1-4 years in clinical lab |
The Histology Laboratory Technician/Technologist will interface directly with laboratory personnel to drive the utmost quality and throughput of Invitae’s offering. Responsibilities include: Must perform clinical patient testing, assay validation testing and quality control testing along with applicable assay documentation according to all laboratory procedures under the direct supervision of a General and/or Technical Supervisor unless they too qualify for that position. Collaborate with research and development personnel in the development and optimization of new histology protocols and clinical assays. Responsible for following laboratory procedures and schedules for specimen handling and processing, test performance, analyses, and reporting and maintaining records of patient test results as well as all safety and compliance regulations | 6/21/2019 |
| 15029 | Invitae San Francisco, CA Assay Tools Bioinformatics Engineer BS/BA in biological sciences or related Exp: 0-2+ years |
As part of our Assay Tools team, you will help ensure that we can grow the breadth and scale of genetic tests on our menu. You will apply your knowledge of computer science, statistics, and NGS to analyze, improve, and develop an expanding set of modern assays. You will work and learn among an extraordinary set of peers: bioinformaticians, molecular biologists, and software engineers. Your work will directly impact early development work focused on improving the quality and capability of our products. | 6/21/2019 |
| 15030 | ThermoFisher Greenville, NC Formulation Technician II HS Diploma Exp: 1+ year in manufacturing |
Sets-up, operates, and maintains the classified environments and manufacturing equipment for pharmaceutical products. Requires proficiency in; cleaning and sterilizing equipment, gowning and aseptic techniques, preparing equipment and components for operations, operating and troubleshooting mechanical equipment, following approved procedures and proper documentation. | 6/21/2019 |
| 15031 | ThermoFisher Greenville, NC QC Scientist BS/BA in life sciences/chemistry Exp: 0-2 years related experience |
Job duties include: Provide routine analyses in a chemistry or microbiology environment by following standard practices. Perform analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and/or human cells. Support internal development and/or manufacturing operations. Make detailed observations and review, document, and communicate test results. Conduct routine chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods. | 6/21/2019 |
| 15032 | ThermoFisher Greenville, NC QC Scientist I BS/BA in life sciences/chemistry Exp: 0-2 years related experience |
Job duties include: Provide routine analyses in a chemistry or microbiology environment by following standard practices. Perform analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and/or human cells. Support internal development and/or manufacturing operations. Make detailed observations and review, document, and communicate test results. Conduct routine chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods. | 6/21/2019 |
| 15033 | ThermoFisher San Jose, CA Failure Analysis Engineer BS or MS in electronics or equivalent Exp: 0-2 years related experience |
The ideal candidate has a strong background in LC/MS products and a strong technical understanding of the hardware and technology. This role with play a major factor in the development of technology critical to supporting Thermo Fisher Scientific’s position as the leader in mass spectrometry in our San Jose, CA facility. Duties include; Perform detailed root-cause-analysis and work with cross-functional teams on improvements or preventative actions, along with various miscellaneous responsibilities. Perform a failure analysis of LCMS products and parts for medical device regulatory requirements.Work with R & D to ensure new products meet product design criteria for serviceability and develop hardware validation criteria. | 6/21/2019 |
| 15034 | ThermoFisher Allentown, PA Project Support Associate HS Diploma Exp: 1+ year as project manager |
Duties include: Applies Good Manufacturing Principles in all areas of responsibility. Initiates the involvement of appropriate departments and maintains continuous communication with those departments. Evaluates customer clinical research packaging specifications the customer and/or Project Manager II/III or Senior Project Manager. Responsible for learning and mastering all internal systems associated with projects. (i.e JOTS (job order tracking syste, SFDC (sale force.com, etc. | 6/21/2019 |
| 15035 | ThermoFisher Fremont, CA QC Engineer/Scientist I BS/BA in chemistry/biochemistry Exp: 0-2 years in QA/QC |
Major responsibilities include: Performs routine testing and analysis of components and finished kits according to established Quality Control procedures using different instrument platforms. Documents test results, complete batch records, document problems and other relevant information under cGMPs. Performs initial troubleshooting of issues which arise during routine analysis, perform out of specification (OOS investigations) and if needed, initiate non-conformance (NCAR) reports. Performs initial troubleshooting of issues which arise during routine analysis under the direction of the Supervisor and Technical Operations. | 6/21/2019 |
| 15036 | ThermoFisher Greenville, NC QC Scientist I Nightshift BS/BA in related Exp: 0-2 years lab experience |
Perform Environmental Monitoring in support of production activities in classified areas. Job function includes aseptic technique including aseptic gowning working in cleanrooms to monitor the area while sterile products are filled and manufactured. Performs analyses including instrumental and automated methods utilizing prescribed procedures and techniques. Generates valid data, reports results on appropriate database compared to established specifications while adhering to GMPs. Compares laboratory results with specifications for acceptability and determines if repetition or OOS is required. | 6/21/2019 |
| 15037 | iRhythm Lincolnshire, IL Sales Associate BS/BA Exp: 1-2 years in sales support |
This role will primarily focus on outbound initiatives including research and evaluation of various health care systems, identifying key medical and administrative contacts, competitive intelligence gathering, and appointment setting. A successful Sales Associate will enjoy making outbound calls to educate medical professionals about iRhythm products and services. | 6/21/2019 |
| 15038 | Iridex Corporation Mountain View, CA Jr. QA Engineer BS in engineering or equivalent Exp: 1-3 years in quality/reliability engineering |
The Quality Assurance department is devoted to assuring safe, reliable and effective products that exceed patient, physician and hospital/clinic expectations. The department plays a vital role in product and process quality supporting commercial production for all Iridex products including laser consoles, delivery devices and accessories. The Quality Engineer (QE) works with a team of dedicated individuals supporting new product development and manufacturing operations to assure quality of finished product and identify quality issues related to electrical, mechanical and software subsystems. The QE evaluates product quality issues, performs root cause analysis, identifies remedial actions and follows up to ensure all actions are completed satisfactorily prior to resolution and closure. | 6/21/2019 |
| 15039 | Genetech South San Francisco, CA PV Operations Associate BS/BA in life sciences Exp: 0-12 years in PV |
Key accountabilities include: Perform reconciliation related activities for Market Research Patient (MAP) support programs and responsible for tasks related to MAP Global Tracking Tool (GTT) to ensure continuous data integrity. Run operational metrics reports on a routine basis, identify follow-up’s required, and work with the appropriate PV Operations head and/or vendor lead to ensure appropriate follow-up is completed. Responsible for executing Source Data QC (SDQC) of in scope MAPs on a quarterly basis. This includes: a) Communication with MAP vendors; b) management of vendor conducting SDQC, including appropriate QC; receiving, QC and tracking data files. | 6/21/2019 |
| 15040 | Genetech Vacaville, CA Manufacturing Technician - BioProcess AS/BS/BA in biological, physical sciences, or engineering Exp: 0-2 years |
Responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment; maintaining areas in high state of inspection preparedness, and utilizing business systems for inventory and process management. Maintain records to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Participate in the routine production of mammalian cell culture products within the Vacaville Manufacturing Facility, operating in at least one of the following production areas: | 6/21/2019 |
| 15041 | Jubilant Cadista Salisbury, MD Maintenance Technician HS Diploma or AS/AA in technical discipline Exp: 0-2 years |
Essential functions include: Thoroughly assess any problems with the process equipment, identifies the problems, makes necessary repairs and completes all associated GMP documentation required to appropriately record the work performed in order to minimize equipment downtime. Participates in cross functional teams to identify assignable root causes for any product or equipment related deviations or anomalies, establish and implement necessary corrective and preventive actions needed to ensure the incident or anomaly is prevented in the future. Coordinates routine and non-routine maintenance within the master production schedule, work closely with manufacturing personnel to obtain information needed to assess equipment problems in a courteous professional demeanor, as well as working with other Maintenance Technicians. | 6/21/2019 |
| 15042 | Catalent Madison, WI Biomanufacturing Solution Prep, Associate 1 AS/AA or HS Diploma Exp: HS: 1+ years, AS: 0 years |
Catalent has an entry level Associate, cGMP Manufacturing position available. As an Associate, cGMP Manufacturing (Good Manufacturing Practices) you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document cGMP Biomanufacturing activities. Shift position is Wednesday to Saturday (4/10) from 7:00 a.m. to 5:00 p.m. CST. Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). | 6/21/2019 |
| 15043 | Catalent St. Petersburg, FL Laboratory Technician HS Diploma Exp: 0-2 years lab experience |
The Laboratory Technician will support the needs in the laboratory for the Product Development department, including raw material sampling/ordering, maintaining inventory of supplies in the lab, preparing dissolution & HPLC media, maintaining equipment in a qualified/calibrating state, contacting vendors for equipment maintenance, working with the scientist to assist with daily lab experiments and helping to prepare samples, lead lab waste management initiatives and act as a safety officer for the lab, etc. | 6/21/2019 |
| 15044 | Catalent Madison, WI Associate, Biomanufacturing Operations BS/BA in biotechnology Exp: 0 years |
As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position offering enticing compensation incentives. Work hours are Wednesday to Saturday (4/10). Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) revisions, deviation investigations and change control/protocol execution, by established due dates. As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position offering enticing compensation incentives. Work hours are Wednesday to Saturday (4/10). Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) revisions, deviation investigations and change control/protocol execution, by established due dates. As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position offering enticing compensation incentives. Work hours are Wednesday to Saturday (4/10). Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) revisions, deviation investigations and change control/protocol execution, by established due dates. | 6/21/2019 |
| 15045 | Catalent Madison, WI Associate I, cGMP Biomanufacturing AS/AA or HS Diploma Exp: HS: 1+ years, AS: 0 years |
The Associate I, cGMP Biomanufacturing is responsible for current Good Manufacturing Practices (cGMP) production activities, including Master/Working Cell Bank production, Upstream cell culture, Downstream protein/mRNA purification, and/or Fill/Finish. This position is a Sunday - Wednesday, 6:00 am – 4:30 pm shift. Responsibilities include: Performs aseptic techniques within in a clean room environment. Executes and properly documents cGMP Biomanufacturing activities. Operates cGMP Biomanufacturing equipment, including pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and analytical equipment as applicable. | 6/21/2019 |
| 15046 | Catalent Madison, WI Associate I, Solutions Prep AS/AA or HS Diploma Exp: HS: 1+ years, AS: 0 years |
The Solutions Prep, Associate I will perform aseptic techniques within in a clean room environment. Execute and properly document cGMP Biomanufacturing activities. The Solutions Prep, Associate I will operate cGMP Biomanufacturing equipment, including pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and analytical equipment as applicable. The position is expected to follow detailed instructions and established procedures with frequent supervision. Shift position is Sunday - Wednesday (4/10) from 7:00 a.m. to 5:30 p.m. CST. The Solutions Prep, Associate I will perform aseptic techniques within in a clean room environment. Execute and properly document cGMP Biomanufacturing activities. The Solutions Prep, Associate I will operate cGMP Biomanufacturing equipment, including pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and analytical equipment as applicable. The position is expected to follow detailed instructions and established procedures with frequent supervision. Shift position is Sunday - Wednesday (4/10) from 7:00 a.m. to 5:30 p.m. CST. The Solutions Prep, Associate I will perform aseptic techniques within in a clean room environment. Execute and properly document cGMP Biomanufacturing activities. The Solutions Prep, Associate I will operate cGMP Biomanufacturing equipment, including pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and analytical equipment as applicable. The position is expected to follow detailed instructions and established procedures with frequent supervision. Shift position is Sunday - Wednesday (4/10) from 7:00 a.m. to 5:30 p.m. CST. | 6/21/2019 |
| 15047 | Celgene Warren, NJ Clinical Manufacturing Associate CAR-T BS/BA in sciences or engineering Exp: 0-2 years |
Manufacture human blood derived cell therapies per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment of a multi-product clinical facility under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. | 6/21/2019 |
| 15048 | Just BioTherapeutics Seattle, WA Associate Scientist, Analytical BS in chemistry/biochemistry Exp: 0-3 years |
Responsibilities inlcude: Utilize chromatography data systems and informatics platforms to analyze and distribute analytical results. The successful candidate will have some experience in chromatography, electrophoresis, and analytical chemistry. Experience with high throughput analytical testing, statistical analysis and high-performance liquid chromatography is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. | 6/21/2019 |
| 15049 | Just BioTherapeutics Seattle, WA Associate Scientist, Quality Control BS in chemistry/biochemistry Exp: 0-3 years |
We are looking for a someone to join a fast-paced, collaborative, and multidisciplinary team to provide QC analysis of raw material, in-process and drug substance testing in support of our GMP operations. The successful candidate will have some experience in analytical chemistry. Experience with chromatography and ELISA techniques is a plus. The ideal candidate has a high attention to detail, is organized in their work and works well independently and in teams. Perform QC analytical testing in support of the GMP manufacturing schedule and drug substance release | 6/21/2019 |
| 15050 | Purigen Biosystems Pleasanton, CA Research Associate I/II BS in Molecular Biology, Biology, Biochemistry or similar Exp: 1-3 years |
Purigen Biosystems, Inc., a Venture-backed, life science tools start-up company in the San Francisco bay area, is seeking an experienced Research Associate to join our Operations team. The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. This is a hands-on position for the highly qualified, self-motivated candidate who wants to enable cutting-edge life sciences technologies in a fast-paced, start-up environment. Responsibilities: Set up and maintain mammalian cell line cultures and prepare cell samples by harvesting, cell-counting and lysing cells. Execute new and standard protocols for performance testing of Purigen’s custom Sample Preparation platform, including instrumentation and microfluidic chip prototypes. etc. | 6/21/2019 |
| 15051 | Pyramid Laboratories unspecified, Manufacturing Technician No degree required. Exp: 1+ years |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. PRINCIPAL DUTIES: Familiar with related GMP procedures and requirements, as directly related to the position. Ensure that appropriate procedures and processes are utilized without unauthorized modifications. Ability to set-up, maintain and perform various manufacturing related activities as required for a GMP compliant Fill/Finish operation. | 6/21/2019 |
| 15052 | QPS Newark, DE Associate Scientist I - Biotransformation BS in chemistry, biochemistry or related discipline Exp: 0-2 years |
Whether their focus is on small molecules, proteins, antibodies, vaccines or oligonucleotides, QPS provides our clients with a full range of services to support the entire spectrum from early discovery, to IND-enabling ADME, to clinical studies. An Associate Scientist in our DMPK department will be a fully-supervised trainee, responsible for formulations, and sample processing and analysis to support preclinical drug discovery and development. Essential Functions: Assist with quantitative and qualitative bio-analytical studies by conducting sample preparation with various analytical chemistry methodologies. Perform routine lab operations, such as sample extraction, preparing reagents, pipette, weigh, monitor, record, label tubes, order and maintain inventory of supplies, and timely disposal of study samples, in a neat/clean manner. etc. | 6/21/2019 |
| 15053 | QPS Newark, DE Associate Scientist I - Protein Binding BS in chemistry, biochemistry or related discipline Exp: 0-2 years |
Whether their focus is on small molecules, proteins, antibodies, vaccines or oligonucleotides, QPS provides our clients with a full range of services to support the entire spectrum from early discovery, to IND-enabling ADME, to clinical studies. An Associate Scientist in our DMPK department will be a fully-supervised trainee, responsible for formulations, and sample processing and analysis to support preclinical drug discovery and development. Essential Functions: Assist with quantitative and qualitative bio-analytical studies by conducting sample preparation with various analytical chemistry methodologies. Perform routine lab operations, such as sample extraction, preparing reagents, pipette, weigh, monitor, record, label tubes, order and maintain inventory of supplies, and timely disposal of study samples, in a neat/clean manner. etc. | 6/21/2019 |
| 15054 | QPS Fargo, ND Associate I, QC - Part-Time BS Exp: 0-1 year |
Through its Dermal and Transdermal Research Laboratory (DTRL), located in Fargo, ND, QPS has considerable expertise in the field of topical and transdermal pharmacokinetics, safety, and efficacy testing. We provide our clients a range of specialized research services for the pharmaceutical, cosmetic and toxicology industries. Based in Fargo, ND, this part-time staff member will be key in ensuring that all data produced by DTRL is documented in an accurate, complete, and timely manner. Essential Functions: Review all study documentation for accuracy and completeness. Monitor data and documentation on an ongoing basis, and prepare QC audit reports of findings. Inspect study documentation for evidence of non-compliance with protocols, SOPs or applicable regulations. etc. | 6/21/2019 |
| 15055 | QPS Newark, DE Associate Scientist I AS/BS in analytical chemistry, biochemistry, pharmacology or related field Exp: 0-2 years |
Whether their focus is on small molecules, proteins, antibodies, vaccines or oligonucleotides, QPS provides our clients with a full range of bioanalytical solutions to support the entire spectrum from early discovery, to IND-enabling ADME, to clinical studies. An Associate Scientist in our Bioanalytical department will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. If you have a Bachelor’s degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmacology, or other related disciplines and want to be part of an organization and industry that is making a difference, we would like to hear from you. | 6/21/2019 |
| 15056 | QPS Newark, DE Associate I, Sample Coordination HS diploma Exp: 1+ years |
The Sample Coordination Associate is a key member of QPS’ DMPK team, ensuring that client samples and other controlled materials are received, stored, distributed, tracked and returned safely, securely, confidentially and without loss or damage. This role requires comfort with computer systems and databases, and requires independence, attention to detail, organization, and juggling multiple tasks. Essential Functions: Manage study samples according to GLPs and SOPs, including: Sample receipt - Completing inventory, documenting discrepancies, storing, and communicating with team as appropriate. Sample pulling for basic runs, boxing samples after analysis, and sample tracking as needed. etc. | 6/21/2019 |
| 15057 | QPS Springfield, MO Data Management Associate HS disploma/BS Exp: 6+ months |
The Data Management Associate is an entry level position within the functions of the Data Management Department, including the maintenance of trial related source documents, as well as the timely reporting of clinical data to clients and/or regulatory authorities. The Data Management Associate must possess strong time management skills in order to effectively compile and manage source documents, perform data entry, QC source documents and transcribed data, participate in client interaction and requests, and perform short term or long term projects as required by the department manager and/or department supervisor within contractual timelines. etc. | 6/21/2019 |
| 15058 | IQVIA Marietta, GA Entry Level Clinical Trial Project Coordinator BS/BA in project management or life sciences Exp: 0-2 years |
The Project Coordinator provides support to the Project Manager and related team members by performing generic procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. startup, maintenance and close-out); Ensure work is conducted in line with standard operating procedures, policies and good practices. Oversee and manage the timely closure of queries and work with the internal applicable teams or functional areas where applicable (examples may include, the Global Delivery Network, Contact Center or being the point of contact for client personnel to assist with service queries, including related to investigator reports). | 6/21/2019 |
| 15059 | IQVIA San Francisco, CA Entry-Level Pharmaceutical Sales Representative BS/BA Exp: 0-2 years |
The primary objective of the sale representative is to meet established sales goals by delivering real value to our customers through differentiated products and services. The sales representative will be supported in this initiative with tools and promotional resources designed to have local impact. The successful representative will demonstrate the ability to target and manage their territory strategically while operating within an assigned budget. They will also need to be a highly engaged, positive team player and show a high degree of customer focus. | 6/21/2019 |
| 15060 | IQVIA Valencia, CA Histologist 1 HS Diploma Exp: 1+ years lab experience |
Under the supervision of Manager medical lab, this role will be Perform gross trimming of tissues and organs systems, processing, paraffin embedding, and sectioning for pathological analysis in our pathology laboratory. According to policies and procedures, perform routine and non-routine activities involved in the preparation of slides, for microscopic evaluation by pathologist(s). Secure the slice sample on a slide and use specialized dyes to stain it, bringing out cellular structures and allowing pathologists, or research scientists to identify abnormal cells and monitor cell function. | 6/21/2019 |
| 15061 | IQVIA Durham, NC Site Support Engineer I BS/BA in computer science or related Exp: 1+ year with PC software |
Under general supervision, provide hands on support to local end-users, to restore service and / or identify and correct core problem. Responsibilities include: Recreate user problems to resolve operating difficulties and recommend system modifications to reduce user problems. Escalate more complex problems to appropriate level of management and provide information on problems that are severe in nature or that are exceeding target dates. Adhere to established IT policies, procedures and standards and ensure conformance with information systems, goals and procedures. Provide creative, effective solutions and recommend procedures and resources to enhance efficiency, productivity, and end user satisfaction. etc. | 6/21/2019 |
| 15062 | Prometrika Cambridge, MA Database Programmer BA/BS Exp: 1 year in database design and Medidata RAVE |
RESPONSIBILITIES: Build eCRFs, including dynamics and matrices in Medidata RAVE. Quality check database structures in accordance with the annotated eCRF. Write and edit check programming in Metidata RAVE. Custom function programming preferred. Perform other database related duties as assigned. | 6/20/2019 |
| 15063 | Protagonist Therrapeutics unspecified, CA Clinical Trail Assistant BA/BS Exp: 1+ years as a CTA |
Core Responsibilities: Reviews, processes, and tracks study related documents (e.g. CVs, FDA 1572s, lab certifications, IRB approvals, contracts etc.) obtained directly and/or through vendors. Sets-up and maintains the Trial Master File (TMF). Maintains and disseminates basic study tracking information including, but not limited to: Visit Reports, Regulatory Documents, Site and Team Contact Lists. Prepares, ships and manages inventory of study related supplies. Gathers investigator and site information (addresses, contact numbers, fax numbers, personnel names and email addresses, etc.) Assists in preparing materials for investigator and team meetings, study manuals etc. Core Responsibilities: Reviews, processes, and tracks study related documents (e.g. CVs, FDA 1572s, lab certifications, IRB approvals, contracts etc.) obtained directly and/or through vendors. Sets-up and maintains the Trial Master File (TMF). Maintains and disseminates basic study tracking information including, but not limited to: Visit Reports, Regulatory Documents, Site and Team Contact Lists. Prepares, ships and manages inventory of study related supplies. Gathers investigator and site information (addresses, contact numbers, fax numbers, personnel names and email addresses, etc.) Assists in preparing materials for investigator and team meetings, study manuals etc. Core Responsibilities: Reviews, processes, and tracks study related documents (e.g. CVs, FDA 1572s, lab certifications, IRB approvals, contracts etc.) obtained directly and/or through vendors. Sets-up and maintains the Trial Master File (TMF). Maintains and disseminates basic study tracking information including, but not limited to: Visit Reports, Regulatory Documents, Site and Team Contact Lists. Prepares, ships and manages inventory of study related supplies. Gathers investigator and site information (addresses, contact numbers, fax numbers, personnel names and email addresses, etc.) Assists in preparing materials for investigator and team meetings, study manuals etc. | 6/20/2019 |
| 15064 | ProteinSimple (Biotechne) Minneapolis, MN Research Associate BS in biotechnology or equivalent Exp: 0-2 years |
This position is for the production of a Bio-Techne product line. Duties include; Aseptic technique for the manufacture of sterile buffers. Extraction, centrifugation and dialysis of product from various materials. Sterile fill and finish in a clean room environment. Labeling and Inventory control of products. Daily and weekly maintenance of the clean room environment. Future GMP production and additional duties as assigned. Key Responsibilities: Aseptic technique, Dialysis, Buffer preparation, GMP Production. etc. | 6/20/2019 |
| 15065 | ProteinSimple (Biotechne) Minneapolis, MN Kit Packer 1 HS diploma/AS Exp: HS: 0-2 years, AS: 0 years |
The responsibilities of this position are to assemble and shrink-wrap all immunoassay kits manufactured by Dept. 385 to include set-up, label printing, and computer work. Document daily Kit Packing statistics. Review and distribute weekly pack schedule. Bin product inserts in inventory system as needed. Tear down of expired kits. Participate in cycle counts as necessary. Key Responsibilities: Pack all kits per the daily schedule. Set-up for next day’s pack schedule. Print all labels for kits. Inspect components prior to packaging. Inspect and release stand-alone proteins and antibodies. etc. | 6/20/2019 |
| 15066 | ProteinSimple (Biotechne) Minneapolis, MN Research Associate, Cell & Gene Therapy BS or equivalent Exp: 0-2 years |
B-MoGen Biotechnologies is currently seeking to fill the role of a Research Associate (Cellular Therapies) to expand our genome engineering team. This position would focus on completing customer projects, who are interested in transitioning to clinical therapies and or using cells for research and development. Applicants should have a solid understanding of, molecular and cellular biology and will have an emphasis on human pluripotent stem cells. Key Responsibilities: Participate in unique fee-for-service projects for the development, optimization, and manufacture of genetically modified cell lines, primary cells, mouse embryonic stem cells, and human pluripotent stem cells. Create and run flow cytometry panels. etc. | 6/20/2019 |
| 15067 | ProteinSimple (Biotechne) Minneapolis, MN Facilities Maintenance Mechanic 1 HS diploma or equivalent Exp: 1-2 years |
The responsibilities of this position are to perform preventative maintenance and repair malfunctioning new and existing minor equipment. Respond and log supervisory alarms on TAC Monitoring System during business hours. Act as the secondary facility maintenance mechanic responsible 24/7 on call for TAC & Security System with department personnel. Assist with installing new and existing equipment, offices furniture and shelves. Perform additional duties as assigned. Key Responsibilities: Performs scheduled preventive maintenance on minor equipment and tasks covered under "Checks" assigned by RAM System and completes all necessary documents once work is complete. etc. | 6/20/2019 |
| 15068 | ProteinSimple (Biotechne) Minneapolis, MN Advanced Research Associate, Conjugation MS in chemistry, biological science or equivalent Exp: 0-2 years |
This position is responsible for preparing conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel. Key Responsibilities: Prepares conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research according to written and non written procedures. Prepares and tests other chemistry related reagents for company personnel according to written and non written procedures. etc. | 6/20/2019 |
| 15069 | ProteinSimple (Biotechne) Minneapolis, MN Customer Service Representative - Temporary BA/BS in Business, Sales, Marketing or Life Sciences Exp: 1-3 years |
This is a great opportunity to get started with a quickly growing biotech company in Minneapolis! The responsibilities of this position are to answer sales and customer inquiries for availability and order status, pricing, and other order-related questions. ESSENTIAL FUNCTIONS: Enter emailed orders into ERP System. Primary point-of-contact to customer questions related to their order. Ensure customer’s needs and expectations regarding their order are met. Follow through with requests to completion or escalate to Customer Care Specialist when appropriate. etc. | 6/20/2019 |
| 15070 | ProteinSimple (Biotechne) Minneapolis, MN Customer Service Representative - Specialist Team BA/BS in Business, Sales, Marketing or Life Sciences Exp: 1-3 years |
This is a great opportunity to get started with a quickly growing biotech company in Minneapolis! The responsibilities of this position are to answer sales and customer inquiries for availability and order status, pricing, and other order-related questions. ESSENTIAL FUNCTIONS: Enter emailed orders into ERP System. Primary point-of-contact to customer questions related to their order. Ensure customer’s needs and expectations regarding their order are met. Follow through with requests to completion or escalate to Customer Care Specialist when appropriate. etc. | 6/20/2019 |
| 15071 | Provid Pharmaceuticals unspecified, Organic/Medicinal Chemist MS/BS Exp: unspecified |
We are seeking recent graduates and experienced candidates with strong synthetic backgrounds, excellent scientific and communication skills and who have the ability to assume a wide range of responsibilities including program leadership roles. | 6/20/2019 |
| 15072 | PSC Biotech Pomona, CA Validation Engineer (Autoclave) BS Exp: 1-3 years |
We are seeking Validation Engineers with experience qualifying autoclaves. Responsibilities: Knowledgeable and experienced in performing Autoclave validations and mapping. Writing and execution of validation Protocols IQ, OQ, and PQs for Autoclave. Writing and execution of Validation Protocols for Part Washers IQ, OQ and PQs. Calibration of Thermocouples for Temperature Mapping Studies. Calculation and interpretation of data for Equipment Validation Studies. Develop, Review and modify Standard Operating Procedures (SOPs). etc. | 6/20/2019 |
| 15073 | PSC Biotech Orange County, CA Entry Level CSV Engineer BS in chemical or biomedical engineering Exp: previous experience with IT or GxP industries preferreed |
We are looking for an Entry-Level Computer System Validation Engineer to support our client in Irvine, CA. This role would work alongside an amazingly talented PSC Team, and works under the leadership of one of the best in the industry! Successful candidates will have excellent verbal and written communication skills, an understanding of the IT realm, and a thirst to learn! Responsibilities: Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards. Initiate/update GxP and Risk Assessments on system. etc. | 6/20/2019 |
| 15074 | PSC Biotech Pomona, CA Entry Level CSV Engineer BS in chemical or biomedical engineering Exp: previous experience with IT or GxP industries preferreed |
We are looking for an Entry-Level Computer System Validation Engineer to support our client in Irvine, CA. This role would work alongside an amazingly talented PSC Team, and works under the leadership of one of the best in the industry! Successful candidates will have excellent verbal and written communication skills, an understanding of the IT realm, and a thirst to learn! Responsibilities: Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards. Initiate/update GxP and Risk Assessments on system. etc. | 6/20/2019 |
| 15075 | PSC Biotech Pomona, CA Receptionist BA/BS Exp: 1-2 years as a receptionist or administrative assistant using a multiline phone system |
PSC Biotech Corporation is seeking an Administrative Assistant / Receptionist with exceptional interpersonal skills to support the Pomona office. This is an exciting time for PSC as we continue to rapidly grow our work force. We are seeking an energetic individual to serve as PSC headquarters’ ‘first point of contact’ and a helpful “go-to” resource for our employees and clients. This is a great opportunity if you thrive in a changing and fast-paced environment. If you enjoy helping people with a smile, are great on the phone, and performing administrative functions, this is the position for you. You will be responsible for being the first point of contact for our Corporate Office. etc. | 6/20/2019 |
| 15076 | Pulmatrix unspecified, Engineering Associate BS/BA or MS in chemical or biomedical engineering or related field Exp: 1-5 years in biotech/pharmaceutical R&D |
We are seeking a highly motivated engineer to join the Pharmaceutical Development group supporting process development for respiratory drug products. Responsibilities: Support development and optimization of engineered particle inhaled dosage forms. Specific methods may include bench and pilot-scale spray drying. Support development of new technologies. Perform physicochemical property and aerosol performance characterization of solid-based inhalation dosage forms. Support batch manufacture for development, pre-clinical and clinical studies. etc. We are seeking a highly motivated engineer to join the Pharmaceutical Development group supporting process development for respiratory drug products. Responsibilities: Support development and optimization of engineered particle inhaled dosage forms. Specific methods may include bench and pilot-scale spray drying. Support development of new technologies. Perform physicochemical property and aerosol performance characterization of solid-based inhalation dosage forms. Support batch manufacture for development, pre-clinical and clinical studies. etc. | 6/20/2019 |
| 15077 | Purdue Pharma Coventry, RI Lab Technician AS/BS Exp: 1-2 years preferred |
This position will provide technical support to the product development staff as well as maintain the product development laboratory in compliant and working order. This position will primarily provide hands on support in manufacturing finished product dosage forms – tablets, capsules, liquids and semi-solids. This position will be responsible for equipment set up, product manufacturing and cleaning as per EHS, DEA and FDA regulations. In addition to assisting the product development scientists in manufacturing finished product prototypes, general support of the laboratory is required. Support activities will include managing inventories for raw materials, personal protection equipment, supplies, etc. This position will also be responsible for providing escort for equipment qualification with vendors, witnessing controlled substance receiving and dispensing, coordinating laboratory waste disposal and pickup, as well as performing and/or facilitating equipment calibrations. This role may perform other related assignments and duties as required. etc. | 6/20/2019 |
| 15078 | Purdue Pharma Wilson, NC Pharmaceutical Technician, 2nd shift (Granulation/Blending) HS diploma or equivalent Exp: 1-5 years pharmaceutical industry experience or equivalent |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Primary Responsibilities: Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Prepare raw materials, blends, and bulk accountability throughout manufacturing processes. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. Identify, report, and resolve quality issues. Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing and/or packaging equipment (oral solid dose manufacturing and packaging may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.). etc. | 6/20/2019 |
| 15079 | Precision For Medicine Carlsbad, CA Biostatiscian I - Clincal Trial Services MS in Biostatistics/Statistics Exp: entry level |
What to expect day-to-day: Generating randomization schedules and providing sample size calculations. Providing input into development of case report forms (CRFs). Authoring and reviewing statistical analysis plans, including development of table and listing shells. Generating analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. Providing programming support and quality control for SAS Programs and other study documents. Providing statistical analysis and reports to Data Monitoring Committees (DMCs) and preparing clinical study reports. Reviewing output across programs to ensure consistency. Participating in the development and maintenance of SOPs. Serving as the primary project team representative, delegating work as appropriate. Training and mentoring new statisticians. etc. | 6/19/2019 |
| 15080 | Precision For Medicine Costa Mesa, CA Copywriter, Healthcare Advertising Agency BS/BA Exp: 1+ years in a healthcare agency environment |
As the primary “storyteller” for your assigned brands, the copywriter partners with senior writers as well as creative leaders to properly understand, articulate and develop copy. Working in a wide variety of mediums, including but not limited to print, collateral, video, digital, etc., you will ensure our content is consistent with the established strategy, brand guidelines, and industry standards. You’ll: Participating in the creation of the brand narrative, from the ground-up. Presenting creative to clients and core constituents. Engaging in productive dialogue as it pertains to brand strategy, narrative arch, and copy to ensure alignment; real-time as necessary with both internal and client teams. Participate in all concepting sessions; taking a standard creative brief to create a varied and deep set of creative entry points. etc. | 6/19/2019 |
| 15081 | Precision For Medicine Chicago, IL Medical Writers - Entry & Mid-Level - Payer Marketing/Market Access Agency BS/BA in English or life sciences discipline Exp: 1-3 years |
We form teams of Medical Writers across varying levels of experience to deliver a range of medical services, including researching, developing, and writing content. You will write medical content for our clients who are developing groundbreaking medicines and treatments. Join us to make a difference in making medicines accessible and affordable. Are you an experienced writer in the medical or pharmaceutical communications industry? Do you get excited working with a respected team that ensures the highest writing quality in the work crafted for top pharma clients? If so, this is where you come in. What Your Day-To-Day Will Look Like: Writing high-quality, medically accurate print or digital documents. Acting as a subject matter authority on the supported therapeutic areas. Procuring, organizing, and handling reference materials from a various sources including peer-reviewed scientific journals, government and medical society publications, and reputable websites. etc. | 6/19/2019 |
| 15082 | Precision For Medicine Gladstone, NJ Medical Writers - Entry & Mid-Level - Payer Marketing/Market Access Agency BS/BA in English or life sciences discipline Exp: 1-3 years |
We form teams of Medical Writers across varying levels of experience to deliver a range of medical services, including researching, developing, and writing content. You will write medical content for our clients who are developing groundbreaking medicines and treatments. Join us to make a difference in making medicines accessible and affordable. Are you an experienced writer in the medical or pharmaceutical communications industry? Do you get excited working with a respected team that ensures the highest writing quality in the work crafted for top pharma clients? If so, this is where you come in. What Your Day-To-Day Will Look Like: Writing high-quality, medically accurate print or digital documents. Acting as a subject matter authority on the supported therapeutic areas. Procuring, organizing, and handling reference materials from a various sources including peer-reviewed scientific journals, government and medical society publications, and reputable websites. etc. | 6/19/2019 |
| 15083 | Precision For Medicine Carlsbad, CA Programmer I - Clinical Trial Services BS in statistics, mathematocs, computer science or related field Exp: entry level |
What to expect day to day: Create specifications for derived/analysis datasets. Program analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. Generate SDTM domains, ADaM datasets, and Define.xml files. Provide programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests. Perform quality control for SAS programs and other study documents (e.g., presentations and reports). Document the quality control review process. Review output across programs to ensure consistency. Review, maintain, and approve study documents per standard procedures. | 6/19/2019 |
| 15084 | Precision For Medicine Oakland, CA Research Scientist MS Exp: 1 year conducting health economic research |
We are excited to invite motivated Research Scientists to consider a career with us. You will provide evidence based-research to life sciences and healthcare companies to shape strategy and inform key healthcare decisions. Successful candidates will have excellent problem solving and analytical skills; a commitment to teamwork and collaboration; an ability to communicate complex concepts to non-technical audiences; and a willingness to deliver high quality results under tight deadlines. What you can expect day-to-day: Using statistical methods and data visualizations to analyze real-world healthcare data. Creating slide decks, reports, and manuscripts that summarize the results of quantitative analyses. Helping develop simulation models for disease burden, comparative effectiveness, or cost-effectiveness studies. Collaborating across a broad portfolio of sophisticated health economic and health policy research projects. etc. | 6/19/2019 |
| 15085 | Precision For Medicine Vancouver, BC Research Statistician - HEOR MS Exp: 1-3 years |
As an Associate Research Statistician you will develop and implement advanced research across a broad portfolio of evidence synthesis and decision modeling research projects. Associate Research Statisticians collaborate with project teams to execute analytical work, as well as contribute to the development of the department as a whole. Essential duties include but are not limited to: Conducting meta-analyses and network meta-analyses. Conduct statistical analyses to support projects. Draft interim and final project deliverables for clients. Clearly interpret and communicate complex quantitative results to internal and external audiences. etc. | 6/19/2019 |
| 15086 | ICON Farmingdale, NY Sample Mgmnt Coordinator HS Diploma Exp: 1-2 years |
Responsible for coordinating the shipment of diagnostic samples as per client specific requirements. Maintaining sample integrity at all times, ensuring correct procedures are followed and correct documentation accompanies the shipment of samples. Quality checking of shipments to ensure correct samples are included and documentation accompanies shipments. Shipment of samples to other ICL locations or referral laboratories per protocol specific requirements. Coordinate courier collections with Logistics to ensure shipments are sent as per protocol specific requirements | 6/15/2019 |
| 15087 | ICUMED Salt Lake City, UT Equipment Operator I HS Diploma/GED Exp: 0-1 years |
A Equipment Operator I is responsible for the safe and efficient operation of simple automated assembly machines. This individual will ensure the continued operation of assembly machines through interpretation of and appropriate response to machine faults and through infrequent alignment of stations and fixtures. This individual will perform simple, repetitive tasks associated with machine operation and will operate machines that require a low level of attentiveness. The operator is also responsible for ensuring that medical devices are assembled with the highest quality possible. | 6/15/2019 |
| 15088 | ICUMED Salt Lake City, UT Quality Inspector I HS Diploma/GED Exp: 0-1 years |
Independently performs inspections on parts, materials, and supplies received from vendors, perform in-process production inspections, and ensure products comply with quality standards prior to shipment. Issues acceptance or rejection tags based on outcome of inspections, checking with supervisor on more difficult determinations. Familiar with manufacturing environment, inspecting, testing, sampling, and sorting of products / goods being manufactured. | 6/15/2019 |
| 15089 | Imbed Biosciences Fitchburg, WI Production Technician, Medical Device Manufacturing BS/BA in sciences/technical field Exp: 1-4 years |
Technician will assist Manufacturing team in production of medical devices. Successful candidate will work within a high-energy, small, focused team environment and maintain a strong sense of shared responsibility and shared reward to make work fun and interesting. Work with Medical Device Production team in a moderate-volume commercial laboratory to fabricate polymeric films, perform and assist in daily laboratory tasks and work flow, maintain and edit standard operating procedures and work instructions, record data, write reports and communicate results. Ensure quality control of materials and end products of the company in a consistent manner. | 6/15/2019 |
| 15090 | Immucor Inc Norcross, GA Medical Laboratory Technologist I AS or BS/BA in sciences Exp: 0-1 years |
As a Medical Technologist I, you will perform all assigned tasks following applicable laboratory SOPs, OSHA regulations and cGMP regulations (i.e. blood borne pathogens and chemical hazards). You will assist the department supervisor and/or manager with investigations, root cause analyses, and reports of out-of-specification results and deviations. You will also be responsible for maintaining and compiling Device History Records. | 6/15/2019 |
| 15091 | Immucor Inc Mountain View, Ca Research Associate BS/BA Exp: 1-3 years research experience |
As a Research Associate, you will be responsible for performing a variety of standard molecular biology techniques such as the extraction, isolation, and identification of biological molecules that are relevant to the generation of important clinical information using molecular methodologies such as polymerase chain reactions, real-time PCR, sequencing technologies, and standard or novel methodologies for protein detection. | 6/15/2019 |
| 15092 | Immucor Inc Norcross, GA Laboratory Technician AS in biomedical engineering, or biomedical technology Exp: 1 year experience |
As a Laboratory Technician, you will be responsible for performing routine and preventative maintenance on all Automated Instrumentation in the R&D labs. You will also maintain and order department supplies and raw materials for R&D labs including stocking supplies and performing cycle counts. Repairing and replacing parts as necessary on all automated instrumentation in R&D labs. Assuring all personnel are in compliance with all departmental laboratory procedures, OSHA safety regulations and other safety related procedures. | 6/15/2019 |
| 15093 | Immucor Inc Norcross, GA Solid Phase Technician AS/AA in life sciences, engineering, or automation Exp: 0-1 years |
As a Solid Phase Technician, you are responsible for performing manufacturing operations according to department procedures, specifications or work instructions and completing tasks within procedure/work-instruction-defined time frames. Specific duties include: Preparing reagents as bulk and for use in Manufacturing processes, Following appropriate control measures to prevent mixing of dissimilar solid phase components or products, Following applicable laboratory OSHA safety regulations with respect to chemical hazards, blood-borne pathogens, etc. | 6/15/2019 |
| 15094 | Immunomedics Morris Plains, NJ Validation Engineer BS/BA in engineering or sciences Exp: 1-2 years hands-on validation |
The Validation Engineer will be responsible for the completion of assigned validation projects encompassing equipment, instruments, computers, cleaning, and process areas for the entire validation lifecycle. Satisfactorily completes assigned validation projects. Performs IQ/OQ/PQ of facility, including building management system and appropriate manufacturing and QC equipment; executes process/cleaning and specified system validations. Investigates and writes Notice of Events/Deviations when applicable. | 6/15/2019 |
| 15095 | InCube Labs San Jose, CA Scientist BS in biochemistry or related Exp: 0-3 years research experience |
Research Associate plays a pivotal role in our R & D teamwork on novel projects involving drug-device combinations for treating chronic diseases with the potential to dramatically impact patient outcomes. Responsibilities include: Independently carry out technical aspects of research projects including formulation work, sample preparation, conducting experiments, recording and managing data, and communicating results to supervisors and research team. Conduct bioanalytical assays and analyze data for the quantification of analytes. Record and manage data from complex experiments including preliminary statistical analysis | 6/15/2019 |
| 15096 | Indivior Indianapolis, IN Specialty Pharmaceutical Sales Rep/Clinical Specialist BS/BA Exp: 1+ years in pharma/medical/health sciences |
The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Responsibilities include: Invest the time and the effort to achieve the established goals for the territory such as sales, market share, doctor calls, appropriate program planning, etc. Plan and organize daily sales call activities to optimize the use of time and maximize the achievement of sales objectives. | 6/15/2019 |
| 15097 | Indivior Jacksonville, FL Specialty Pharmaceutical Sales Rep/Clinical Specialist BS/BA Exp: 1+ years in pharma/medical/health sciences |
The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Responsibilities include: Invest the time and the effort to achieve the established goals for the territory such as sales, market share, doctor calls, appropriate program planning, etc. Plan and organize daily sales call activities to optimize the use of time and maximize the achievement of sales objectives. | 6/15/2019 |
| 15098 | Indivior Portland, ME Specialty Pharmaceutical Sales Rep/Clinical Specialist BS/BA Exp: 1+ years in pharma/medical/health sciences |
The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Responsibilities include: Invest the time and the effort to achieve the established goals for the territory such as sales, market share, doctor calls, appropriate program planning, etc. Plan and organize daily sales call activities to optimize the use of time and maximize the achievement of sales objectives. | 6/15/2019 |
| 15099 | Inova Piagnostics San Diego, CA Chemist I - IFA Controls BS/BA in biological or chemical sciences Exp: 0-2 years lab experience |
Assists with preparation of autoimmune diagnostic Immunofluorescence Assay (IFA) slide, control and conjugate products in accordance with established procedures. Major duties include preparation activities for IFA controls and conjugates and the growth of cloned antigens in insect cells. Maintains detailed Device History Records, laboratory notebooks and/or any associated documentation for all manufacturing and evaluation activities in accordance with current Quality Systems Regulations (QSRs). Tests IFA slide products for acceptable titer and pattern reactivity according to written Manufacturing Documents. Assists with the maintenance and growth of insect cells and the harvesting of various cloned antigens from these cells according to established procedures. | 6/15/2019 |
| 15100 | Inova Piagnostics San Diego, CA QC Analyst I BS/BA in biological or chemical sciences Exp: 1+ years lab experience |
This is an entry level position responsible for performing the QC functions for release of intermediate and finished products, including conducting stability studies, according to standard operating procedures. This position will assist in maintaining the work environment in state of compliance for GMP, OSHA and other applicable regulatory requirements. Performs QC testing/inspection of intermediate and finished products according to established house specifications accurately and on time. Inspects labels and finished components and kits to ensure compliance to all requirements before distribution. Assists with the maintenance and proper organization of the QC patient samples to ensure availability of the samples at all times and ease of retrieval. | 6/15/2019 |
| 15101 | Inova Piagnostics San Diego, CA Technical Services Support Specialist I BS/BA in medical technology, biological science, or related Exp: 1-2 years with diagnostics/instruments |
As a member of the Technical Support Team, provides product and technical support to customers via phone and email on all Inova products. Responsible for assessing customers’ needs and delivering exceptional customer service to provide remote support, basic troubleshooting, and issue resolution for Inova customers. Responds to customer product inquires on a broad range of technical questions regarding instrument and assay performance, instrument capabilities, quality control, and other product concerns. Interpersonal skills and technical product knowledge, judgement and decision making expertise are critical to responding to daily customer-centric activities. | 6/15/2019 |
| 15102 | Omnipod Salt Lake City, UT Inside Sales - Omnipod Associate BS/BA Exp: 0-1 years in medical device sales |
This role works closely and collaborates with the field sales and internal team members to provide the best patient experience possible. This role is responsible for communicating insurance benefit guidelines and cost share information with patients and assists them with their decisions regarding insulin pump therapy. Promote and sell Insulet’s products to prospective customers. Responsible for making outbound calls to patients who have expressed interest in the OmniPod System. Responsible for handling inbound calls from patients generated through physicians’ offices or marketing programs. | 6/15/2019 |
| 15103 | Integer Plymouth , MN Manufacturing Engineer I BS/BA in manufacturing, mechanical, or industrial engineering Exp: 0-3 years |
The primary purpose of this position is to perform work which involves conventional engineering practice. Ensures Integer's internal and external customer expectations are met or exceeded. Accountabilities & Responsibilities: Adheres to Integer's Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. | 6/15/2019 |
| 15104 | Integer Plymouth , MN Process Engineer BS/BA Exp: 0-3 years |
Participate in cross-functional project teams to implement creative solutions. Monitors performance of equipment, machines and tools and correct equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. Interfaces with Quality and R&D to integrate new products or processes. Responsible for identifying and correcting manufacturing process nonconformance's identified during prototype builds. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. | 6/15/2019 |
| 15105 | Integer Chaska, MN Manufacturing Team Member I HS Diploma Exp: 0-2 years |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. Assembles component parts as per print. Utilizes both manual and automatic machine operation. | 6/15/2019 |
| 15106 | Integer Chaska, MN Manufacturing Team Member I HS Diploma Exp: 0-2 years |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. Assembles component parts as per print. Utilizes both manual and automatic machine operation. | 6/15/2019 |
| 15107 | Integer Alden, MN Manufacturing Team Member: 1st Shift (Mon - Fri) HS Diploma Exp: 0-2 years |
Primary Purpose: To develop competency in and perform basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Responsibilities include: Set up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Assembles component parts as per print. Utilizes both manual and automatic machine operation. Visually and/or dimensionally inspects parts and/or completed assemblies for conformance to specifications. Identifies and escalates quality non-conformances. | 6/15/2019 |
| 15108 | Integer Trenton, GA SPI Operator I - Weekend Night Shift HS Diploma Exp: 1+ years in manufacturing |
Position summary: Perform most of the tasks and procedures required to ensure the timely and efficient processing of jobs through the manufacturing area. Maintain and update production and material control systems as needed to ensure proper job and material tracking is maintained. Maintain work area and equipment in a clean, neat, and organized fashion. Complete off-schedule notifications. | 6/15/2019 |
| 15109 | Integra LifeSciences Plainsboro, NJ Materials Handler HS Diploma Exp: 0-1 years Quality Inspection |
The individual will be responsible for all material handling on 1st and 2nd shifts as well as aspects of receiving, shipping, inventory control and inventory movement. Other responsibilities include processing returned materials. Transact receipts, shipments, movements and work orders in a MRP system. Use department databases to track and manage Finished Goods and Raw Material Inventories. Effectively follow SOPs, policies and ISO/QSR requirements. etc. | 6/15/2019 |
| 15110 | Integra LifeSciences Plainsboro, NJ Associate Sales Representative, Wound Reconstruction BS/BA Exp: 0-2 years outside sales experience |
The Associate Sales Representative will be a responsible Integra’s Integra Skin and Primatrix 6X6 > product line and solely responsible for supporting these products within for sales of these products for a defined territory within the Hospital OR/Surgery setting. Your primary responsibility will be to support and grow business in order to achieve or exceed sales revenue targets. You will provide case coverage, transport trays, and develop select accounts by building relationships, demonstrating extensive product knowledge and providing exceptional customer service. Your primary call points will be plastic surgeons, podiatric surgeons, orthopedic surgeons, and general surgeons. 50% of your time will be spent in the Operating Room. You will work side by side with an experienced Account Manager for approximately 18 months. | 6/15/2019 |
| 15111 | Integral Medicine Philadelphia, PA Research Associate I BS/BA in biology, bioengineering or related Exp: 1-2 years lab experience |
We seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. Conduct laboratory research and support general R&D efforts for customer-based biomedical research. Projects may involve cell culture, virology, DNA preparation, and liquid-handling automation. Perform cell-based assays (Western blot, ELISA, immunofluorescence, flow cytometry) | 6/15/2019 |
| 15112 | Integral Medicine Philadelphia, PA Biotechnology Sales Associate BS/BA in biology, bioengineering or related Exp: 1+ years lab experience |
We are seeking a Technology Sales Associate to join our Philadelphia-based sales, marketing and business development team. Responsibilities include: Lead generation and data entry into customer relationship management (CRM) system. Conduct marketing and sales efforts targeting large and small antibody biotech customers. Prepare sales reports on product performance. | 6/15/2019 |
| 15113 | Integrated DNA Technologies San Diego, CA Production Scientist I BS/BA in sciences Exp: 0-2 years |
The Production Scientist I synthesizes, purifies, formulates and ensures the quality of custom oligonucleotides according to the customer’s order and internal specifications. This generally includes, synthesis, cleavage, deprotection, purification, desalting, QC sampling, QC analysis and final packaging and formulation of the oligos and chemical reagents being made. | 6/15/2019 |
| 15114 | Integrity Bio Camarillo, CA Quality Control Associate II BS/BA in sciences Exp: 1+ years in QC |
We are currently seeking a QC associate to work in both laboratory and cleanroom environments under strict SOP’s for performing environmental monitoring and other lab testing. Responsibilities include; sampling using EM equipment, sample handling, testing, reporting results with accurate documentation, investigation of OOS’s, and determination of root cause as appropriate | 6/15/2019 |
| 15115 | Integrity Bio Camarillo, CA Research Associate BS/BA in biochemistry, chemistry, biological sciences or related Exp: 1-5 years in biotech/pharma |
Job duties as a research associate include: Assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision. Set up and perform HPLC, as well as other assays, to characterize protein and peptide molecules. Analyzes, records, and reports the results and conclusions for laboratory experiments. Summarizes and interprets data. The candidate should also be open to learn new laboratory techniques and work under the guidance of experienced researchers. | 6/15/2019 |
| 15116 | Integrity Bio Camarillo, CA Manufacturing Associate BS in sciences Exp: 1+ year in biotech/pharma |
Manufacturing Associate will be responsible for the manufacture of pre-clinical/clinical products. Responsibilities include: Operates the production processes according to the determined daily production planning. Performs defined production processes according to GMP and SOP procedures (e.g., set-up, machine handling, close down, reconciliation,line cleaning, line clearance, waste disposal, storage, etc.). | 6/15/2019 |
| 15117 | Intuitive Multiple Locations, US Field Service Engineer AA in electronics or mechanical engineering Exp: 1-3 years field service experience |
Primary Function of Position: Install and support the Intuitive Surgical products and ensure service agreements and warranty obligations are fulfilled. Exceed customer expectations and maintain customer satisfaction to the highest possible level. Responsibilities includes: Pre site verifications to prepare site for system installation. Assist in coordination of system delivery (e.g. confirming site readiness) Troubleshoot and repair Intuitive Surgical products and associated equipment failures as required. etc. | 6/15/2019 |
| 15118 | Intuitive Albany, NY da Vinci Clinical Territory Associate BS/BA, sales preferred Exp: 1+ year in leadership or sales |
The Clinical Territory Associate (CTA) will work closely with the Clinical Sales Manager to gain knowledge in all aspects of our business to include technical, clinical, and sales. He or She will train to be a da Vinci® Surgery technical and sales expert across all primary surgical specialties to develop surgical robotics programs in the assigned territory. During the first year of the job, the CTA will focus on the technical and clinical aspect of the job, and during the second year of the job, the CTA will progress and begin to focus on the sales aspect of the job. The CTA will have the opportunity to support a specific region by maximizing the utilization of installed da Vinci® Surgical Systems by leading product demonstrations/in-services and sales activities. | 6/15/2019 |
| 15119 | Invicro Boston, MA Associate Scientist, in vivo BS/BA in biology, animal sciences, or related Exp: Entry Level |
The open associate scientist position is one that will support all in vivo, small animal medical imaging studies. These studies include nuclear medicine (PET/SPECT), computed tomography (CT), and magnetic resonance imaging (MRI). The Associate Scientist will maintain the animal and imaging facility, provide study support in mouse and rat disease models ranging from basic injections to surgical procedures, and assist in image acquisition procedures. This position will be an immersive cross-functional opportunity where an ideal candidate will identify areas in which to excel and focus a career in research. A qualified applicant is enthusiastic about biomedical research, able and willing to rapidly learn new skills and begin applying them immediately. | 6/15/2019 |
| 15120 | HemaCare Northridge, CA Research Associate BS in biological sciences Exp: 1+ general lab experience |
This position isresponsible for the evaluationof humanblood products for manual orautomated cell isolations, product manufacturer,andcell culture.Perform QC testing and create a certificateof analysis(COA)for products manufactured. Record isolation details on a processing worksheet usinggood documentation practices. Operate flow cytometer and basic lab equipment. | 6/14/2019 |
| 15121 | HemoSonics Charlottesville, VA Associate Research Engineer BS in biomedical engineering or related Exp: 1+ years general work experience |
HemoSonics, LLC is seeking an Associate Research Engineer who will be responsible for the support of concept phase activities, including ideation, feasibility testing, and early development of new product concepts; and the support of development activities. Key responsibilities include: Design and execute feasibility tests, Test, analyze, and interpret data and development situations/events requiring evaluation of identifiable factors, Apply standard principles, theories and concepts in the field and have working knowledge of other related disciplines, etc. | 6/14/2019 |
| 15122 | Heska Des Moines, IA Technician I - Immunotherapy AS in sciences or BS/BA Exp: 0-2 years |
The Immunotherapy Technician I position will work under the close supervision of the Immunotherapy supervisor to carry out the following departmental responsibilities: aseptically filling immunotherapy vials and preparing all products for final packaging and shipment. This position will require the ability to multitask as well as follow standard operating procedures at all times. Performs aseptic hand filling operations, Prepares raw materials and filling operation set-up, Inventories all of the department raw materials and products, etc. | 6/14/2019 |
| 15123 | High Point Clinical Trials Center High Point, NC Lab Supervisor HS Diploma/GED Exp: 1+ years lab experience |
Applicants should have demonstrated team management skills as well as working knowledge of IATA sample shipment processes, CLIA-waivered laboratory processes, and ability to fully manage external vendors for our clinical trial testing needs. This position ensures the full reconciliation of all specimens submitted to outside client and vendors in a manner fully compliant to Good Clinical Practice under FDA guidelines. Responsibilities include: Completes all study procedures as per FDA regulations, GCP guidelines and protocol requirements, Assists with and performs laboratory procedures including sample check-in, preparation, centrifugation, storage and shipment, Assists with temperature monitoring and control of laboratory sample environments, etc. | 6/14/2019 |
| 15124 | High Point Clinical Trials Center High Point, NC Research Nurse Nursing license Exp: 1+ years nursing |
Assist in conduct of clinical studies. Provides licensed nursing coverage for studies and performs procedures as allowed by training and delegation. Duties include: Assist in the conduct of clinical studies while providing licensed coverage. Performs all job responsibilities in accordance with standards of Good Clinical Practice (GCP), clinic standard operating procedures (SOP’s), and OSHA guidelines. Perform tasks such as EKG’s, vital signs, phlebotomy, insertion and maintenance of IV catheters. Communicates in a timely manner with physicians regarding patient safety concerns, adverse events, protocol deviations, and any study conduct issues. | 6/14/2019 |
| 15125 | High Point Clinical Trials Center High Point, NC Paramedic HS Diploma/GED + Active Paramedic license Exp: 1+ years as EMS |
Assist in conduct of clinical studies. Provides licensed nursing coverage for studies and performs procedures as allowed by training and delegation. Duties include: Assist in the conduct of clinical studies while providing licensed coverage. Performs all job responsibilities in accordance with standards of Good Clinical Practice (GCP), clinic standard operating procedures (SOP’s), and OSHA guidelines. Perform tasks such as EKG’s, vital signs, phlebotomy, insertion and maintenance of IV catheters. Communicates in a timely manner with physicians regarding patient safety concerns, adverse events, protocol deviations, and any study conduct issues. | 6/14/2019 |
| 15126 | Hikma Cherry Hill, NJ QA Inspector - QA BS in sciences Exp: 0-2 years lab experience |
The QA Inspector monitors in-process product quality for Filling and Inspection and Packaging of parenteral products. The QA Inspector is responsible for performing visual and functional testing of product against statistically based sampling plans. In addition, the QA Inspector performs routine inspection and testing of components in accordance with Standard Procedures and specifications as required by production scheduling. In performing the above duties, the individual is responsible for accurately and clearly documenting test results in accordance with cGMPs. This position participates in rotation for weekend coverage and as needed during the work week. This is a 3rd shift position | 6/14/2019 |
| 15127 | Hikma Cherry Hill, NJ Fill Operator I HS Diploma/GED Exp: 1+ year operating production equipment |
Using company guidelines, the Filling Operator I is responsible for the full spectrum of duties in controlled filling and ancillary rooms. This may include but is not limited to: set-up, operation, sanitization, equipment cleaning, PM activities, airlock and ancillary room cleaning, etc. Assists with or performs preventive maintenance tasks on filling equipment, such as inspection and cleaning of machine parts, as may be required. | 6/14/2019 |
| 15128 | Hikma Cherry Hill, NJ Quality Lab Associate I, Env. Monitoring BS/BA in microbiology/biology Exp: 0-2 years pharma experience |
This is a 3rd shift position. Perform functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. Responsibilities includes: Ensure Environmental Monitoring (EM) of the facility’s controlled areas is performed as required. Document EM testing into the EM database prior to incubation, ensure samples are correctly incubated, and record sample results in the EM database following incubation. Compile trending data for EM testing to support investigations. Audit personnel aseptic technique in controlled areas including during process simulations (media fills). | 6/14/2019 |
| 15129 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro BS/BA in microbiology/biology Exp: 0-2 years pharma experience |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management. Other responsibilities includes: Use sophisticated laboratory instruments and computer systems to collect and record data. Perform advanced laboratory assays requiring precise analytical and aseptic technique skills. Work on special projects and protocol testing that involves new methods and instrumentation. Complete all special projects and protocol testing in a timely and appropriate manner. | 6/14/2019 |
| 15130 | Hikma Cherry Hill, NJ Project Manager, Clinical Research BS/BA in sciences/technical field Exp: 1-3 years in project management |
Assist with project plan development for clinical research trials. Manage internal and external resources including subject matter experts, doctors, vendors, and drive activities to meet or exceed timelines and milestones. Identify obstacles that may negatively impact clinical trial progress and ideate viable options to maintain project advancement. Direct and manage the clinical trial project from beginning to end. Responsible and accountable for the delivery of project milestones, and maintaining timelines to successful outcomes according to the approved business case on time, expected quality and within budget. Assist with the development of full-scale clinical trial project plans and associated communications documents, and tracking tools. | 6/14/2019 |
| 15131 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro BS/BA in sciences/technical field Exp: 0-2 years pharma experience |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management. Other responsibilities includes: Use sophisticated laboratory instruments and computer systems to collect and record data. Perform advanced laboratory assays requiring precise analytical and aseptic technique skills. Work on special projects and protocol testing that involves new methods and instrumentation. Complete all special projects and protocol testing in a timely and appropriate manner. | 6/14/2019 |
| 15132 | Hologic San Diego, CA Oligo Process Development Chemist 1 BS Exp: 0-2 years in QSR/GMP |
Responsible for the manufacture of GMP oligonucleotides; the continuous improvement of these existing oligo processes; and the development/transfer of new oligo processes. Provides oligo process support to Operations group through instrument/oligo process troubleshooting and completion of NCR investigations. Responsible for research, development and production manufacturing activities associated with oligos.Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. | 6/14/2019 |
| 15133 | Hologic San Diego, CA Operations Test Associate BS/BA Exp: 0-3 years lab experience |
We are currently seeking an Operations Test Associate responsible for generating accurate and reliable data for biologic products or medical devices on stability. Responsibilities include: Performs routine stability testing using GMP/GLPpractices. Performs data analysis and results interpretationscomparing to stability protocol defined specifications, validity criteria, and alertlimits. Responsible for the maintenance and cleanliness ofthe laboratory, stocking shelves/drawers with testing materials. Prepares documents for storage in our documentmanagement system and manages original data files. | 6/14/2019 |
| 15134 | Hologic San Diego, CA Process Development Associate 1 BS/BA Exp: 1+ years |
Responsible for the creation and transfer of manufacturing processes from R&D to Manufacturing and continuous improvement of existing processes.Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Maintains the Pilot Plant laboratory under cGMP conditions. Produces development, pilot and production materials per written instructions, Completes ERP transactions, Stocks and maintains the laboratory supplies, Keeps accurate records and documentation, Completes laboratory work and associated paperwork by assigned completion dates, etc. | 6/14/2019 |
| 15135 | Hologic San Diego, CA Process Development Associate 1 BS/BA Exp: 1+ years |
Responsible for the creation and transfer of manufacturing processes from R&D to Manufacturing and continuous improvement of existing processes.Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Maintains the Pilot Plant laboratory under cGMP conditions. Produces development, pilot and production materials per written instructions, Completes ERP transactions, Stocks and maintains the laboratory supplies, Keeps accurate records and documentation, Completes laboratory work and associated paperwork by assigned completion dates, etc. | 6/14/2019 |
| 15136 | Hologic San Diego, CA Oligo Process Development Chemist 1 BS or equivalent Exp: 0-2 years |
Responsible for the manufacture of GMP oligonucleotides; the continuous improvement of these existing oligo processes; and the development/transfer of new oligo processes. Provides oligo process support to Operations group through instrument/oligo process troubleshooting and completion of NCR investigations. Responsible for research, development and production manufacturing activities associated with oligos.Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Independently produces notebook, dev, pilot and production materials per written directions. Analyzes in-process and final oligos using state of the art analytical techniques | 6/14/2019 |
| 15137 | Hologic San Diego, CA Microbiology Research Associate 2-3 BS or equivalent Exp: 1-3 years industry experience |
The Research Associate 2/3 will perform basic and advanced culture techniques, including microbiology, tissue culture and virus culture in support of assay development activities as well as product support activities. This includes sterile aerobic as well as anaerobic work technique and involves handling of infectious materials. Performs moderately complex experiments with input from supervisor. Understands experimental goal and exhibits critical thinking skillswhen evaluating data. Interprets experimental results in context of overall experimental goal, etc. | 6/14/2019 |
| 15138 | Hologic San Diego, CA Research Associate 2 BS/BA or MS in molecular biology, chemistry, biochem, or related Exp: BS: 1-3 years, MS: 0 years |
Hologic is seeking a Research Associate responsible for designing and performing experiments while collaborating and communicating effectively. Responsibilities include: Understands experimental goal and exhibits critical thinking skills when evaluating data. Able to summarize related groups of experiments. Provides input to the experimental design. Performs moderately complex experiments with input from supervisor. Interprets experimental results in context of overall experimental goal. etc. | 6/14/2019 |
| 15139 | Homology Medicines Inc. Bedford, MA Research Asscoiate, Analytical Development MS in biological sciences Exp: 0-4 years in QC |
Homology Medicines is seeking a Research Associate to aid in operational support for methods to characterize AAV vector products. The individual in this role will be a talented and motivated technician who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. This is a largely laboratory-based position with a focus on providing analytical support for characterizing research-grade vectors. Plans and executes AAV-specific characterization assays, including vector genome quantification by qPCR and ddPCR, viral capsid quantification by ELISA, protein analysis by SDS-Page gels, endotoxin testing and additional assays as needed | 6/14/2019 |
| 15140 | Homology Medicines Inc. Bedford, MA Research Associate, Downstream Process Development BS in chemical engineering, biochem, or bioengineering Exp: 0 years |
The successful candidate will be an integral part of a fast paced and rapidly growing group of scientists and engineers developing purification processes for the manufacture of Homology’s novel and proprietary adeno-associated virus (AAV) viral vectors. Responsibilities will include helping to develop scalable unit operations supporting viral vector purification such as chromatography, filtration and ultrafiltration. Critical to this role is the ability to concisely interpret and summarize data and to be able to effectively communicate results through high quality technical reports and oral presentations. | 6/14/2019 |
| 15141 | Hovione Hovione, NJ QC Analyst- Drug Product BS/BA in chemistry or related Exp: 0 years |
The Quality Control Analyst ensures all Quality Control (QC) activities at Hovione LLC are carried out in compliance with Corporate Operating Procedures (COP), Standard Operating Procedures (SOP), Internal Operating Procedures (IOP), and Federal Food and Drug Administration (FDA), International Conference on Harmonization (ICH), Occupational Safety and Health Administration (OSHA), and Environmental Protection Agency (EPA) requirements. Responsibilities include: Perform analytical testing (i.e. raw materials, intermediates, API, stability, cleaning, method validation and cleaning) in a timely manner to meet deadlines; Execute qualification tests contained in protocols for equipment qualification; Perform instrument calibrations on Balances, High Pressure Liquid Chromatography (HPLC) and Gas Chromatography (GC); Carries out routine tasks, routine housekeeping related to the laboratory, and maintenance of analytical equipment. | 6/14/2019 |
| 15142 | Hovione Hovione, NJ Process Technician - Drug Product Continuous Manufacturing BS in engineering (chemical engineering preferred) Exp: 1-2 years in process operations |
The Process Technician will support the installation and qualification of a GMP continuous tablet manufacturing line, highly automated, with Process Analytical Technology enabled control. This position will also support the development and manufacturing activities for drug product and formulation development projects. Main responsibilities include: Work in a GMP environment area, executing chemical and physical operations following approved written instructions and in accordance with cGMPs and EHS regulations. Clean/verify proper cleaning of equipment and production areas according with cGMPs. Adhere to the necessary gowning requirements and in alignment with the various room classifications. Ensure that performed activities are recorded in applicable documentation. | 6/14/2019 |
| 15143 | Hovione Hovione, NJ Process Engineer BS in chemical engineering, chemistry or related Exp: 1-3 years industrial experience |
The Process Engineer will ensure that the use of the best process engineering knowledge will be applied in scaling up chemical and spray drying projects to maximize customer satisfaction and Hovione’s interests and in compliance with all Federal, State, Local and internal policies. Main responsibilities include; Plan and design manufacturing processes based on chemical procedures to run safely and effectively in a pilot plant/kilo lab in accordance with the best known practices ensuring cGMP compliance. Contributes to the Process Hazard Analysis (PHA) of all processes under his/her responsibility and assures that all identified hazards are addressed prior to performing any activities within operations. Prepares Mass balance sheet, instructions for unit operations, production batch records, Bill of Materials and other GMP related documentation for all processes run in operations. etc. | 6/14/2019 |
| 15144 | Hovione Hovione, NJ Associate Quality Assurance Specialist BS in chemistry or chemical engineering Exp: 1-2 years in cGMP industrial environemnt |
The Quality Assurance Associate Specialist promotes high quality standards and a continuous improvement culture within the Quality area of the New Jersey site in order to ensure that these are aligned with applicable quality regulations and the company's high quality standards. This role provides support in achieving the department objectives and supports the cGMP programs (i.e. validation, qualification, stability, and environmental control). Main responsibilities include: Reviews completed batch records and associated deviations for final product release; Reviews executed protocols and other GMP related documentation; Responsible for evaluation/approval of equipment cleaning; Prepares SOPs, quality related reports, and change control documents when appropriate; etc. | 6/14/2019 |
| 15145 | HTG Tucson, AZ Operations Laboratory Technician I AS or BS/BA in sciences Exp: AS: 1-2 years, BS: 0-1 years |
The successful candidate will have responsibilities for reviewing and updating lab quality control processes, reviewing and analyzing results of tests to improve product quality level and maintaining product inventory. Tasks will include preparing product for internal and external customers and operation, maintenance and calibration of laboratory equipment. They will utilize standard procedures to formulate, test, fill and assemble product. Operates and maintains automated laboratory equipment, such as pipettors, scales, incubators, PCR/qPCR instruments and nucleic acid sequencers. Assembles reagents, kit orders, and other products for shipment to customers in accordance with standard protocols. Formulate reagents and solutions utilizing Standard Operating Procedures (SOP’s) and approved Work Instructions (WI’s). etc. | 6/14/2019 |
| 15146 | PRA Health Sciences Phoenix, AZ Client Delivery Analyst, Custom Analytics BS Exp: 1-3 years work experience in a data analytics environment |
The Client Delivery Analyst leads independent data analysis, preparing comprehensive reports and presentations of data analysis findings for internal and external clients per established service level agreements. Job functions include understanding of data inputs to dimension, executing programs, assessing data accuracy, drawing research conclusions, and formatting and presenting output. This person is an expert in recommending procedural changes or participating in new project implementation from start to finish. Furthermore, they will support new client implementations and ad-hocs to support revenue needs. etc. | 6/14/2019 |
| 15147 | Precision BioSciences Durham, NC Research Assistant - Molecular Biology BS Exp: 1+ year experience with relevant laboratory bench work |
Precision BioSciences is seeking a detail oriented molecular biologist with recent laboratory experience for a Research Assistant position. The position will be responsible for routine cloning, DNA preparation and manipulation of bacterial and mammalian cells. The candidate must be a fast learner, meticulous and have a track record of successful bench work. The position is working closely with a large, friendly team in a fast-paced, collaborative environment. As a member of the Core Technology team, the Research Assistant will be responsible for: cloning a variety of constructs into plasmid DNA, plasmid DNA purification, genomic DNA purification, PCR, generation of electrocompotent bacteria. etc. | 6/14/2019 |
| 15148 | Precision BioSciences Durham, NC Research Assistant - In Vivo AS, BS or MS Exp: 0-3 years |
Under specific direction, the Research Assistant, In Vivo Models will assist and perform a variety of routine technical procedures related to the execution of animal studies including: animal identification, colony management, injection of cells and new constructs, imaging, monitoring animal behavior, collecting specimens and euthanasia. May perform tasks related to the research project independently, but within specific guidelines. Strong communication skills and comfort in interdisciplinary lab required. Some evening and weekend work required. etc. | 6/14/2019 |
| 15149 | Precision for Medicine Oakland, CA Associate Research Economist MS or equivalent in economics or related discipline Exp: 0-1 years |
The Associate Research Economist is responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. The Associate Research Economist will have a familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and the ability to utilize specific discipline knowledge gained through academic and/or work experience (e.g. economics, etc.). This position will perform a wide range of activities including: literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. etc. | 6/14/2019 |
| 15150 | Precision for Medicine Los Angeles, CA Associate Research Scientist - Health Policy MS Exp: 1 year conducting health economic research |
What you can expect day-to-day: collaborating across a broad portfolio of sophisticated health economic and health policy research projects, performing a wide range of activities including: literature reviews; regression analysis; preparing content for reports and manuscripts, slide decks and meeting notes; quality assurance/review; and other activities. | 6/14/2019 |
| 15151 | Precision for Medicine Oakland, CA Associate Research Scientist - HEOR MS Exp: 1+ years in a research role |
As an Associate Research Scientist, you will responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. You will have a basic familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and will execute a wide range of activities including: project management; literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. etc. | 6/14/2019 |
| 15152 | Precision for Medicine Boston, MA Associate Research Scientist - HEOR MS Exp: 1+ years in a research role |
As an Associate Research Scientist, you will responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. You will have a basic familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and will execute a wide range of activities including: project management; literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. etc. | 6/14/2019 |
| 15153 | Precision for Medicine Vancouver, BC Associate Research Statistician - HEOR MS Exp: 1-3 years |
As an Associate Research Statistician you will develop and implement advanced research across a broad portfolio of evidence synthesis and decision modeling research projects. Associate Research Statisticians collaborate with project teams to execute analytical work, as well as contribute to the development of the department as a whole. Essential duties include but are not limited to: conducting meta-analyses and network meta-analyses, conduct statistical analyses to support projects, draft interim and final project deliverables for clients. etc. | 6/14/2019 |
| 15154 | Precision for Medicine Indianapolis, IN Business Intelligence Analyst - Pharmaceutical Analytics BS Exp: 1-3 years using Microsoft SQL Server |
Ready to take your technical and data analysis skills and use them to tackle problems facing clients in the pharma & biotech space? Are you proficient in SQL development? Do you have a positive, can-do attitude, are self-motivated and take excellent pride in your work product? If yes, then your dream job is waiting and we'd love to talk to you. We are excited to bring a bright, motivated Business Intelligence Analyst onto our growing team. Read on to learn more about the day to day responsibilities. etc. | 6/14/2019 |
| 15155 | Precision for Medicine Costa Mesa, CA Copywriter, Healthcase Advertising Agency BS/BA Exp: 1+ years in a healthcare agency environment |
As the primary “storyteller” for your assigned brands, the copywriter partners with senior writers as well as creative leaders to properly understand, articulate and develop copy. Working in a wide variety of mediums, including but not limited to print, collateral, video, digital, etc., you will ensure our content is consistent with the established strategy, brand guidelines, and industry standards. You’ll: participate in the creation of the brand narrative, from the ground-up, present creative to clients and core constituents, engage in productive dialogue as it pertains to brand strategy, narrative arch, and copy to ensure alignment. etc. | 6/14/2019 |
| 15156 | Progenity Irving, TX Medical Billing Trainee BS/BA Exp: 1+ years in a billing office or recent graduate degree |
The Medical Billing Trainee works within the Billing and Reimbursement department to understand the revenue cycle and provide strategic insight. This person is dedicated to career growth and is looking to learn more about the functions of a business and how each department works together. Responsibilities: receives training and performs duties focused on improving the revenue cycle, learns various staff functions, including operations, management viewpoints, and company policies and practices affecting each phase of business, meets performance goals and objectives set by upper management and determined upon accepting position. etc. | 6/14/2019 |
| 15157 | Progyny unspecified, NY Cash Application & Payroll Specialist BS/BA in accounting or finance Exp: 1-2 years cash application expericence |
What you'll do... Cash applications: timely and accurate application of daily payments received against outstanding invoices in the General Ledger, accurately report Member AR aging report and Member cash received by Month, perform other duties and special projects as assigned. Payroll: process semi-monthly payroll for all employees (hourly and salaried), provide routine monthly reports requested from payroll. etc. | 6/14/2019 |
| 15158 | Progyny unspecified, NY Business Analyst BS/BA Exp: 0-2 years |
What you'll do... Build automated reports to support internal and external data requests. Build interactive dashboards in Cognos or PowerBI to increase both operational effectiveness and senior management decisions across functions supported by BI: patient care services, provider relations, claims management, network contracting, pharmacy, sales, account management, legal and marketing. You will need to understand the business’ goals, know how to find the data measuring the effort put into meeting those goals, and analyze the information to find trends. etc. | 6/14/2019 |
| 15159 | Promega Madison, WI Environmental, Health & Safety Technician AA/BS in life sciences, chemistry, environmental, or related field Exp: 0-2 year experience working with hazardous materials |
Assist and support the Environmental, Health and Safety (EH&S) department by performing tasks that ensure a safe workplace and sustain Promega’s compliance with Local, State, and Federal environmental, health, and safety regulations. ESSENTIAL DUTIES: 1. Collect chemical, biological, and radiological waste from satellite accumulation areas in all facilities. 2. Properly identify, segregate, process, label and store chemical, biological, and radiological waste according to standard operating procedures and applicable regulations. 3. Schedule, organize and oversee the packaging, labeling, shipment and disposal of chemical, biological, and radiological waste at all facilities. Complete, track and file hazardous and non-hazardous waste manifests and other shipping papers for chemical, biological, and radioactive waste shipments from all facilities. etc. | 6/14/2019 |
| 15160 | Promega Madison, WI Production Scientist 1 AD or BS in a scientific discipline Exp: 0-3 years |
ESSENTIAL DUTIES: 1. Manufacture a variety of Genetic Identity products so as to meet product specifications. Follow production schedules to assure on-time delivery of product. Understand basic laboratory concepts and perform basic lab techniques. 2. Perform assays to assure that products meet existing requirements for purity, activity and functionality. 3. Follow the quality requirements that relate to area. Demonstrates good documentation practices and consistently produces quality products and documentation. Follow existing policies for data recording and record keeping. 4. Understands and complies with ethical, legal and regulatory requirements applicable to our business. etc. | 6/14/2019 |
| 15161 | PharPoint Research unspecified, NC Clinical Data Manager AS required, BS preferred in science or computer related disciplines Exp: 1 year experience in clinical data management |
Perform the execution of Clinical Data Management functions with delegated authority. Interactively participate in the day to day development of the client deliverables while providing supervision and mentorship to Data Management Interns. | 6/12/2019 |
| 15162 | Physical Sciences Inc. Wilmington, MA Battery Scientist BS Exp: 0-2 years |
Physical Sciences Inc., with offices located in Andover and Wilmington, is looking for an entry level Scientist to support advanced Lithium ion battery research and development programs at its Wilmington facility. The individual will be involved in day-to-day hands-on laboratory experimentation, data collection, and analysis. The responsibilities for this position include: battery scientist, assist in the development of advanced anode, cathode, separator and electrolyte components for next generation Li-ion batteries, perform routine lab operations including preparing electrode slurries and building cells for electrochemical evaluation, collect, analyze and present data and findings in informal and formal reports, follow safety procedures and prepare standard operating procedures for new processes developed. | 6/12/2019 |
| 15163 | Physical Sciences Inc. Andover, MA Energetic Formulations Chemist BS/MS in chemistry Exp: MS unspecified; BS work experience in RDT&E in related disciplines |
Physical Sciences Inc., located just north of Boston in Andover, is looking for a chemical scientist to conduct research, development, test and evaluation (RDT&E) of innovative energetic materials for propulsion and munitions systems. Emphasis is placed on laboratory scale and pilot scale processing of ingredients and formulations for fuels, oxidizers, propellants, and explosive compositions. We are seeking an individual with a strong background in wet chemistry and analytical instrumentation to join a multi-disciplinary team of engineers and scientists. This individual will play a key role in growing a diverse portfolio of technologies funded by the DoD and NASA. etc. | 6/12/2019 |
| 15164 | Platelet BioGenesis Cambridge, MA Research Associate, Gene Editing BS/MS in biology, molecular biology, cell biology or immunology Exp: 1-3 years lab experience, in vivo is a plus |
We make platelets. We have developed and patented a microfluidic bioreactor and shown that functional platelets can be generated from human induced pluripotent stem cell cultures. We are now scaling platelet production for human clinical trials and leveraging our platelet platform for cell-based drug delivery. The successful Research Associate will join our Designer Platelet Team, working directly on optimizing and characterizing our drug delivery platform, and providing support for ongoing and emerging research projects. The ideal candidate has experience with platelets, pluripotent stem cells, genetic engineering and enjoys working with a team of scientists in a fast-paced and highly matrix environment. etc. | 6/12/2019 |
| 15165 | Plexxikon Berkeley, CA Research Associate 1, Medicinal Chemistry BS in chemistry Exp: up to 2 years hands-on, relevant experience in organic synthesis |
The Research Associate 1, Medicinal Chemistry will be a critical member of the research team reporting directly to one of our Scientists. This is an exceptional opportunity to gain experience in a successful biopharmaceutical company and bring drugs from ideas to the clinic. Responsibilities include, but are not limited to: Multi-step synthesis, purification and characterization of small molecules for evaluation as potential drug candidates, maintain various lab equipment, maintain current knowledge of synthetic methodology through literature readings, present progress at chemistry group and project team meetings. etc. | 6/12/2019 |
| 15166 | PMI BioPharma Solutions Nashville, TN Chemist I, Analytical Development BS in chemistry, biology, or related science Exp: 1-2 years of pharmaceutical experience |
PMI Biopharma Solutions is looking for an Analytical Development team member that is passionate and driven regarding his/her work. PMI Biopharma Solutions desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. The Chemist I position, reporting to the Director, Analytical Development, will operate under moderate supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development. etc. | 6/12/2019 |
| 15167 | PMI BioPharma Solutions Nashville, TN Facilities Technician I, MSAT unspecified Exp: 1-2 years maintenance experience in regulated manufacturing environment (pharmaceutical/biotech preferred) |
PMI Biopharma Solutions is looking for a Facilities Technician team member that is passionate and driven regarding his/her work. PMI Biopharma Solutions is in need of a motivated individual to provide their expertise in the delivery of results for the company and its clients. Reporting to the Supervisor of Engineering, the Facilities Technician will be responsible for PMI’s maintenance and equipment support activities. The Facilities Technician performs with minimal supervision preventive maintenance, demand maintenance and calibration tasks on critical equipment, utilities, and facilities. etc. | 6/12/2019 |
| 15168 | PMI BioPharma Solutions Nashville, TN Microbiologist I, Analytical Development BS in biology or related field Exp: 0-1 years pharmaceutical experience |
PMI Biopharma Solutions is looking for an Analytical Development team member that is passionate and driven regarding his/her work. PMI Biopharma Solutions desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. Reporting to the Microbiology Supervisor, the Microbiologist I will be responsible for performing environmental monitoring sampling of ISO class environments and assisting with preparation, characterization, and identification of environmental isolates. He/she will perform raw material and drug product method development and cGMP testing. etc. | 6/12/2019 |
| 15169 | Portola Pharmaceuticals San Francisco, CA Clinical Data Manager (temporary) BS/MS in relevant field Exp: 1-3 years experience handling clinical research data |
The Temporary Clinical Data Manager will support the Data Management group from study start-up through database lock and clinical study report. The successful candidate will deliver high quality data, on time and on budget. In this role, the candidate will be expected to lead and provide oversight for the execution of data management activities for more than one compound in a therapeutic area. This role will report to the Associate Director, Clinical Data Management. Works collaboratively with Clinical Programmers, Statistical Programmers, Biostatisticians, Clinical Research, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for moderately complex clinical data acquisition, quality checking and reporting. etc. | 6/12/2019 |
| 15170 | Poseida Therapeutics San Diego, CA Process Development Associate MS Exp: 1+ years experience with immunology, molecular biology, or related field |
Poseida Therapeutics, Inc. is seeking an outstanding candidate to join our Cell Therapy Development group at our La Jolla, San Diego, CA location. The Development Associate will be a key member of a dynamic team that develops and implements characterization strategies to support and enable process and clinical development of gene-engineered cell products. This is a lab-based position that will involve hands-on development of clinical manufacturing processes for selecting, gene-modifying and growing T cell subsets. This position will interface with our Research and Development team as well as with outside Contract Manufacturing Organizations. etc. | 6/12/2019 |
| 15171 | PPD Richmond, VA Lab Support Tech Technical AS Exp: 1 year coursework in laboratory science |
Second shift position to perform routine maintenance tasks on laboratory robots, in support of daily lab operations under the direction of a senior staff member. Must be able to maintain a schedule and perform regulated tasks and documentation. The laboratory technician will work with various teams (automation, lab, etc.) to assist in maintenance of laboratory systems and resources and assist with preparation of laboratory reagents, solutions and chores. etc. | 6/12/2019 |
| 15172 | PPD King of Prussia, PA Associate Scientist- ELISA, qPCR BS or equivalent Exp: 1+ years |
As an Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. In this position you will perform a variety of validated or experimental analytical procedures such as ELISA. You love science and have keen observation skills. You are a self-directed learner with excellent attention to detail. You have an inherent scientific curiosity and enjoy working with instrumentation. etc. | 6/12/2019 |
| 15173 | PPD Highland Heights, KY Assoc Sample Coordinator - Global Central Labs HS Diploma or equivalent Exp: 0-1 years |
Part-Time Position. Performs duties and training to acquire the skills required for sample and standard handling in support of the laboratory. Provides support to Sample Coordinator and performs administrative tasks in the Sample Management department. Follows SOPs, applicable client procedures, and fulfills laboratory requests with modest direct supervision. Performs a variety of simple inventory tracking procedures (receipt, check-in, login, labeling, inventory, transport, check-out, etc.) and administrative tasks in support of laboratory operations. Communicates status of tasks to supervisor and/or appropriate laboratory staff. etc. | 6/12/2019 |
| 15174 | PPD Palmer Square, NJ Associate Scientist - Lab Operations Support Tech (Pathology) BS in biology or related field or equivalent Exp: 0-1+ years |
We are seeking a passionate, highly organized, sharp individual seeking to begin a career in Operations in a lab setting. As an Associate Scientist/Lab Ops Tech you will perform a variety of tasks such as arranging supplies and supporting the Immunohistochemistry, Pathology and Histology in the Translational Medicine group. Your role will strictly be laboratory operations, and not include any bench work. You, as the Associate Scientist will assist scientists through tasks such as shipping and receiving, reagent and supply ordering, inventorying and stocking, lab cleanliness, safety, setting up equipment service & maintenance and record keeping for the labs. etc. | 6/12/2019 |
| 15175 | PPD Richmond, VA Associate Scientist - Immunochemistry BS or equivalent Exp: 1+ years |
As an Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Grow your career within the scientific ladder, pursue project management, or develop into a leader. These are just a few career pathways available once you become a part of the PPD team. etc. | 6/12/2019 |
| 15176 | Envigo Indianapolis, IN Maintenance Technician HS Diploma Exp: 1-2 years experience/training |
Maintenance Technicians are responsible for general repairs and maintenance on buildings, structures and equipment. Maintenance Technicians are generally tasked with day-to-day upkeep of facility equipment that provides vital resources for animal breeding. Performs electrical, electronic, mechanical, hydraulic, and pneumatic maintenance and repair of machinery, equipment, and HVAC system. Performs diagnosing malfunctions in machinery and equipment. Performs dismantling, assembling, and installing industrial machinery. etc. | 6/3/2019 |
| 15177 | Envigo Princeton, NJ Analyst, Immunoassay BS/BA or AS/AA Exp: 0-1 yeras |
Responsible for all aspects of validation, sample analysis and data preparation in support of pre-clinical and clinical studies. Ensure all work is conducted in accordance to GLP/GCP regulations. Conduct validation and sample analysis as per study method, in life study plan and or analytical/validation plans and SOPs in accordance to GLP/GCP. Promptly prepare and submit results after analysis. Work as a team and as directed by Study Managers and Lab Managers. Provide status reports on projects and accountable for meeting agreed timelines and performance quality. etc. | 6/3/2019 |
| 15178 | Enzo Farmingdale, NY Medical Technologist - Immunology BS in clinical lab sciences. License by NYSED as Clinica Lab Technolgist required Exp: 1+ year |
The technologist will perform qualitiative and quantitative tests and examinations using various analyzers and/or manual methods. Assist in peforming established quality assurance procedures (quality control testing, instrument function checks and calibrations). Mainatains appropriate documentation and reports irregularities. | 6/3/2019 |
| 15179 | Enzo Farmingdale, NY Medical Technologist- Generalist (Chemistry, Hematology, Coagulation, Urinalysis) BS in clinical lab sciences. License by NYSED as Clinica Lab Technolgist required Exp: 1+ year |
Several shifts avalible. The Medical Technologist will perform qualitative and quantitative tests and examinations using various analyzers and/or manual methods on specimen sources such as blood, urine, and other body fluids using established procedures. They will also be responsible for performing established quality assurance procedures (quality control testing, instrument function checks and calibrations). Maintains appropriate documentation and reports irregularities. | 6/3/2019 |
| 15180 | Epic Laurelton, NY Analytical R&D Scientist MS in chemistry or biochemistry Exp: 1+ years |
Conduct analytical runs for R&D purposes using a set of analytical techniques such as HPLC, UPLC, GC, including writing related protocols and reports. Develop, evaluate, validate analytical methods for raw materials and finished products. Support the transfer of developed and qualified assays to relevant clients. Provide support, as related to analytical, plant trouble shooting/investigations and product regulatory submission. Provide full analytical development support in accordance with cGMP/GLP practices to product development programs within strict timelines to successfully meet internal and client program milestones. Support the AR&D related activities for filing of new ANDA. Support the generation of pharmaceutical development reports and related documentation. | 6/3/2019 |
| 15181 | Abcam Burlingame, CA Research Associate BS/BA in biological sciences Exp: 1+ year working in lab setting |
The position is primarily responsible for the screening and characterization of monoclonal antibodies. The successful candidate will play a hands-on role in the company’s use of a wide variety of analytical assays such as ELISA, flow cytometry, Octet, and HTRF. He or she will partner closely with other team members within the group, assisting with every step of antibody development. The candidate will make observations, analyze data, and interpret results with full supervision. | 6/3/2019 |
| 15182 | ERT Philadelphia, PA Project Coordinator BS/BA or equivalent Exp: 0-2 years, experience is a plus |
Duties include: deliver customer service by providing support using ERT's products. Work and collaborate with project teams in development and delivery of ERT products. Etc. | 6/3/2019 |
| 15183 | Eurofins Fremont, CA Biochemist- Biacore/Protein Binding MS Exp: 1-2 years protein characterization |
Duties include: performing routine biopharmaceutical characterization studies including UV/Vis, size exclusion, cation exchange chromatography. Support other methods such as mass spec, or immuno-based assays. Conduct experiments and record/interpretate data. | 6/3/2019 |
| 15184 | Eurofins St. Charles, MO Associate Scientist AS/AA or BS/BA Exp: 0-1 years |
Duties as an associate scientist include: performs lab work including preparing buffers/reagents/media. Maintain cell cultures in BSL2 lab. Conducts production assays in ADMET, ion channel, immunosignaling, OncoPanel, etc. | 6/3/2019 |
| 15185 | Eurofins Columbia, MO Assistant Scientist I, Method Dev BS/BA in chemistry or life sciences or engineering Exp: 1+ years related experience |
The Associate Scientist I position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments. | 6/3/2019 |
| 15186 | Eurofins Easton, MD Assistant Scientist I, Aquatics BS/BA in chemistry or life sciences or engineering Exp: 1+ years related experience |
Carries out routine experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs). Assist/run toxicology studies, including preparing test solutions and daily maintenance of test systems. Feed, water, and examine animals for signs of illness, disease, or injury sustained in the laboratory. Performs analysis, first level, and peer review of data for accuracy and completeness. | 6/3/2019 |
| 15187 | Eurofins West Point, PA Analytical Scientist BS in biology, chemistry, or related Exp: 1+ year in cGMP lab |
Responsibilities include: Execute experiements utilizing analytical methods to support preclinical pharamceutical product development. Use techniques/instrumentations such as HPLC and spectroscopy. Prepare test solutions, compounds, and reagents. Maintain lab instruments. etc. | 6/3/2019 |
| 15188 | Eurofins San Diego, CA Analytical Chemist BS/BA in analytical chemistry, biochemistry, or pharmaceutical sciences Exp: 1-2 years in lab/research |
Responsibilities include: Develop, qualify and validate analytical test methods for drug products, intermediates and excipients. Design and execute analytical development studies. Write protocols and repors. Maintain and write SOPs. etc. | 6/3/2019 |
| 15189 | Eurofins Lancaster, PA 2nd shift - Pharmaceutical Stability Project Management Specialist BS/BA in sciences, business or related Exp: 0-2 years, experience is a plus |
2nd shift. Responsibilities include: manage all aspects of stability studies assigned by clients. Take responsibilities for quality and TAT of assigned studies. etc. | 6/3/2019 |
| 15190 | Exactech Gainesville, FL Clinical Research Associate AS/AA or BS/BA preferred Exp: 1+ years in clinical research |
Responsibilities include: Monitor the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), GCP, and all applicable regulatory requirements. Conduct visits to assess the qualification of potential investigative sites, initiate sites, instruct site personnel on the proper conduct of studies and use of Electronic Data Capture (EDC) system, review and ensure accuracy of data collected, and terminate studies | 6/3/2019 |
| 15191 | Exelixis Alameda, CA Risk Analyst BA in business admin, finance, risk management or related Exp: 1-2 years in insurance, project management or consulting |
The Risk Analyst will provide appropriate business risk assessments, identify areas of risk of loss, quantify the impact, develop and evaluate policies and provide guidance to the Company’s decision makers. The Risk Analyst is important role within the organization to minimize the impact of operational and financial risk to the enterprise. | 6/3/2019 |
| 15192 | Exsurco Wakeman, OH Assembly Technician HS Diploma Exp: 0-1 years factory work |
Primary role is to perform all forms assembly activities including equipment setup and tear down where required as well as in-process verifications. In addition, this position includes several cross-functional responsibilities comprising Shipping, Receiving, Job Picking, Warehousing and Plant Cleaning and some Maintenance activities. This position also has responsibilities associated with Servicing returned products (disassembly and reassembly, diagnosis and report writing). | 6/3/2019 |
| 15193 | First Light Diagnostics Chelmsford, MA Research Associate - Microbiology BS in bioengineering, biochemistry, microbiology or related Exp: 0-2 years, experience is a plus |
Candidates should love laboratory science and should enjoy technology innovation. You will work with a group of creative inventive scientists on developing novel state-of-the-art methods that are the basis for important new products to improve medical outcomes for patients with serious infections. Responsibilities include: developing experimental designs, preforming microbiological/molecular biological experiments, and other lab-related work. | 6/3/2019 |
| 15194 | Fluidigm Markham, CA Reagent Manufacturing Associate I BS/BA in biology, biochemistry, or related Exp: 1-2 years in lab/research |
The Reagent Manufacturing Associate is a member of our Proteomics Reagent Operations team. The scientist will be accountable for QC testing of raw materials, in-process materials and finished goods for release. This individual will also be a subject matter expert in the development and testing of new QC procedures. | 6/3/2019 |
| 15195 | Fluidigm South San Francisco, CA Research Associate - Microfluidics BS/BA or MS in chemistry, biomedical engineering or related0-3 years Exp: |
Responsibilities as a research associate include: serving as a key member for testing, analyzing, and developing microfluidic devices. Integrate biochemical reactions in microfluidics. etc. | 6/3/2019 |
| 15196 | Fluidigm Markham, CA Product Development Scientist MS in immunology, molecular biology, biochemistry, or related Exp: 1+ years in research |
The Product Development Scientist will play an active role in developing high-quality Fluidigm reagents. Responsibilities include: write application, product or system validation test plans. Work with product managers and product applications group. Ensure all valudation tests are in concordance with customer and product requirements. etc. | 6/3/2019 |
| 15197 | Fluke Everett, WA Test Engineer BS in electrical engineering or related Exp: 0-2 years |
Responsibilities as a test engineer at Fluke iclude: plan/implement test systes for new product introductions. Support/maintain/improve test systems throughout factory. Advise design engineering of existing production capabilities. etc. | 6/3/2019 |
| 15198 | Fluke Houston, TX Medical Physics Assistant MS Exp: 0-4 years |
Basic Duties and Responsibilities: Assisting in clinical medical physics coverage, as well as supporting the commissioning team's project | 6/3/2019 |
| 15199 | Foxx Life Sciences Salem, NH Wuality Engineer BS in engineering or related Exp: 1+ years in quality engineering |
Duties include: develop and implement all quality-related processes and documentation. Direct manufacturing process development to meet quality metrics. Monitor faility performance and associated metrics. Etc. | 6/3/2019 |
| 15200 | Fresenius Kabi Melrose Park, IL Validation Engineer BS/BA in science or engineering Exp: 1-3 years in cGMP |
Responsible for providing technical support to operations in terms of equipment/system/process initial validation and equipment/system/process requalifications. Will participate in process and equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. Individual must also perform HEPA filter integrity/velocity testing and critical area (class 100) airflow pattern testing. The individual must have a comprehensive understanding of cGMPs and become certified to enter Controlled Areas of the plant (class 100, 10,000 and 100,000). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 6/3/2019 |
| 15201 | Fresenius Kabi Grand Island, NY Associate Scientist - Chemistry Technical Services BS or higher Exp: 1+ years |
Reports to manager, QC chemistry technical services. Responsibilities include: Method transfers/method verification/Co-Validations of compendial and non-compendial analytical methods utilized across Fresenius Kabi according to written procedures. Testing of routine and non-routine samples where specialized training is essential. etc. | 6/3/2019 |
| 15202 | Freudenberg Jeffersonville , IN Medical Device Assembly/ Manufacturing Associate - 1st Shift HS Diploma Exp: 0-1 years |
Responsibilities include: hand assembly manufactured components, complete required documentation for work performance, quality inspect work performed. etc. | 6/3/2019 |
| 15203 | Freudenberg Gloucester, MA Program & Quoting Engineer BS/BA in mechanical engineering or related Exp: 1+ years (coops and internships) |
Ensures that opportunities introduced are a strategic fit to the Lead Center. Coordinates costing activities with the Project Management Team. Ensures that all cost assumptions and cost drivers are optimized and technically feasible. Understands cost assumptions and challenges cost drivers where appropriate. Develops pricing and submits final quotes to the sales team. Establishes acceptable pricing for new business opportunities by optimizing minimum margin requirements and target pricing from the Business Development team. Leads quote meetings within the lead center and acts as the single point of contact at the Lead Center for the Commercial Team specific to the support of new business opportunities. Ensures that all quotations consider Lead Center resources, capabilities, profitability, strategic plan, and product liability and insurance concerns. Utilizes Salesforce.com as the single CRM (customer relationship management) tool for inputs and outputs to the quoting process. Measured by accuracy, clarity, and timeliness of quotation. | 6/3/2019 |
| 15204 | Fujifilm College Station, TX EHS Specialist I BS/BA in safety science, environmental science/engineering or related Exp: 1+ years |
Responsibilities include: Assist with all aspects of EHS, including applicable OSHA regulations, environmental record keeping, safety audits, and accident investigations. Ensure the Emergency Response Plan remains current with regulatory requirements and site needs, assist with the readiness of FDBT personnel and facilities to respond to emergencies. Conduct environmental and safety audits and inspections; assist EHS Management with reporting to Senior Leadership. | 6/3/2019 |
| 15205 | Fujifilm College Station, TX Downstream Manufacturing Technician I AS/AA in biological sciences or engineering Exp: 0-1 years |
The Downstream Manufacturing Technician I will work directly with viral purification (either whole particle or split particle), continuous flow centrifuge operation, and sucrose gradient separation, techniques for filtration and chromatographic separation (i.e. column chromatography and HPLC) and viral inactivation. | 6/3/2019 |
| 15206 | Edwards Irvine, CA Quality Engineer II MS in engineering or sciences Exp: 1-2 years w/medical devices |
Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Responsibilities include: Key Responsibilities: Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports. etc.Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Responsibilities include: Key Responsibilities: Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports. etc.Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Responsibilities include: Key Responsibilities: Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports. etc.Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Responsibilities include: Key Responsibilities: Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports. etc. | 5/31/2019 |
| 15207 | Edwards Irvine, CA Technician, R&D/QA Engineering - Transcatheter Heart Valve AS or equivalent Exp: 1+ years required |
The R&D Technician will support a wide range of engineering activities such as test, check-out, modification, fabrication and assembly under minimal supervision of Engineers and may propose technical solutions. Responsibilities include: Build complex prototypes, sub-assemblies, test samples, and prepare feasibility test units, samples, and/or chemical solutions. Perform complex work using drawings, diagrams, written and verbal instructions, layouts or defined plans to perform testing, checkout, and trouble-shooting functions. | 5/31/2019 |
| 15208 | Edwards Draper, UT Manufacturing Engineer I BS/BA in engineering or sciences Exp: 0-2 years |
Applies knowledge of technical principles and Edwards systems/procedures to tptimize manufacturing processes. Responsibilities include: Improve manufacturing processes using engineering methods for concinous process improvement. Develop basic experiements and tests to qualify and validate manfactruing process, etc. | 5/31/2019 |
| 15209 | Eisai Woodcliff Lake, NJ Clinical Trial Assistant BS in life sciences or related Exp: 1-3 years in clinical operations or related |
Supports all phases of clinical study activities including: TMF review, assist with filing and archiving project documentation in theTMF within a 20 day timeframe. Assist with creating, updating and maintaining project trackers in EPIC. Provides support for document preparation. Attend internal study team meetings, and prepare and distribute study team agendas and minutes. etc. | 5/31/2019 |
| 15210 | Eisai Woodcliff Lake, NJ Clinical Trial Assistant BS in life sciences or related Exp: 1-3 years in clinical operations or related |
Supports all phases of clinical study activities including: TMF review, assist with filing and archiving project documentation in theTMF within a 20 day timeframe. Assist with creating, updating and maintaining project trackers in EPIC. Provides support for document preparation. Attend internal study team meetings, and prepare and distribute study team agendas and minutes. etc. | 5/31/2019 |
| 15211 | Elanco na, IN Associate - Corporate IT Auditor - Fixed Duration Employee BS/BA in computer sciences/engineeirng Exp: 1+ years in audit or IT operations |
The auditor works with 2-5 person audit teams on domestic and global audits designed to test compliance with good internal control practices, external regulations, and corporate policies and procedures, in alignment with Institute of Internal Audit standards. Responsibilities include identifying and assessing risks, scoping engagements, testing policy compliance, automating test procedures, influencing action plans, partnering with affiliate management and audit team members to complete and improve audit processes, sharing of best practices and key learning across the organization. | 5/31/2019 |
| 15212 | Elanco Clinton, IN Mfg Engineering Associate BS/MS engineering Exp: Entry Level (graduating by August 2019) |
Multiple positions. Position titles include but are not limited to Plant Engineer, Process Engineer, Project Engineer, Development Engineer, Automation and/or Control Engineer, and are available in manufacturing and development areas supporting: Bulk processing (Animal health products), facilities/utilities engineering, process development. | 5/31/2019 |
| 15213 | ELITechGroup Bothell, WA Shipping and Receiving Associate HS Diploma Exp: 0-1 years |
Verifies and keeps records on outgoing shipments and prepares items for shipment. Receives product and inspects items to ensure conformance to specifications. Duties include: Confirming shipped/received products/packages. | 5/31/2019 |
| 15214 | Elstar Cambridge, MA Research Associate / Senior Research Associate - Immunology BA or MS in biology or related Exp: 0-3 years |
The successful candidate will be responsible for developing and performing cell-based assays within the Immunology team achieving common team goals. Responsibilities include: Perform ex-vivo and in-vitro cellular assays with an emphasis on flow cytometry and immuno-assays including ELISA and MSD. Analyze and interpret data and generate high-quality summary reports in a timely manner, and present findings in the inter and intra departmental group meetings. Document experimental data and results and maintain a current and accurate electronic notebook (ELN) | 5/31/2019 |
| 15215 | MilliporeSigma Rockville, MD Flexible Resource Associate Scientist BS/BA or MS in biology/chemistry/related Exp: BS: 1+ year, MS: 0-1 years |
The Flexible Resource Associate Scientist conducts pre-designed assays, makes scientific observations, maintains detailed workbooks and ensures all documentation fulfills generally accepted GLP or GMP industry standards. Functional area and period of deployment to a specific laboratory will be controlled via Sales and Operations Planning process. An individual able to follow the SOPs, protocols and relevant compliance regulations regarding safety procedures, documentation and scientific responsibility. You can maintain an understanding of technological principles and applications of the organization’s services; independently analyze data, interpret results and advise the supervisor and study director of any factors that may affect quality and usefulness of data. | 5/31/2019 |
| 15216 | MilliporeSigma Rockville, MD Associate Scientist BS/BA in sciences (biology, microbiology, chemistry, etc.) Exp: 0-2 years |
The Associate I (ASI) will perform safety testing required to manufacture clinical and commercial products. The ASI is required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Additionally, they are required to maintain a thorough understanding of BioReliance services, technical principles and applications. | 5/31/2019 |
| 15217 | EMD Serono Billerica, MA Associate Scientist - In Vitro Pharmacology BS/BA in biology, immunology, or related Exp: 1+ year with cell culture |
We have an opening for a talented Associate Scientist to join the ImmunoOncology platform at EMD Serono, Billerica, MA. The successful candidate will support the discovery of novel cancer immunotherapies. In his/her role, the candidate is expected to develop and conduct cellular immune assays to characterize small molecules or biologics that modulate the tumor immune environment and enhance the anti-tumor immune response. | 5/31/2019 |
| 15218 | MilliporeSigma Sheboygan Falls, WI Quality Assurance Associate BS/BA in life sciences or chemistry Exp: 0-3 years |
Provide Food Safety and Quality systems support for the Flavors and Fragrances product line while ensuring adherence to GMPs and working to improve the Supplier Quality Management program. The Flavors and Fragrances facility is FSSC 22000 certified as well as ISO900. Responsibilities include: ensuring compliance with FSSC 2200 and ISO9001, support customer complaint management, etc. | 5/31/2019 |
| 15219 | MilliporeSigma Miamisburg, OH Scientist, Production Associate (QC) BS/BA in chemistry or life sciences or engineering Exp: 0-4 years |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Essential functions include: ensure quality through process, perform routine assays/processes and/or unit operations, complete work volume, stay in compliance with change control procedures, improve processes, etc. | 5/31/2019 |
| 15220 | MilliporeSigma Billerica, MA Associate Scientist, Immuno-Oncology BS/BA in biology, immunology, or related Exp: 1+ years in research |
We have an opening for an Associate Scientist to join the Immuno-Oncology platform at EMD Serono, Billerica, MA. The successful candidate will support the discovery of novel cancer immunotherapies. In this role, the candidate is expected to develop and conduct cellular immune assays to characterize small molecules or biologics that modulate the tumor immune environment and enhance the anti-tumor immune response. The Associate Scientist will also develop, evaluate and implement well-controlled in vitro experiments to interrogate target biology, and generate proof of concept data supporting target Go/No Go decisions. | 5/31/2019 |
| 15221 | Emergent BioSolutions Lansing, MI Assistant Manufacturing Associate HS Diploma Exp: 0-1 years in cGMP |
Execute tasks per cGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing qualification block training program. Actively incorporate the Core Values set out by Emergent BioSolutions while performing day to day activities. Maintain state of facility environmental control including: preparation of defined concentrations of cleaning solutions, daily, monthly, quarterly and annual cleaning of manufacturing surfaces and equipment per Standard Operating Procedures. etc. | 5/31/2019 |
| 15222 | Emergent BioSolutions Lansing, MI Assistant Manufacturing Associate HS Diploma Exp: 0-1 years in cGMP |
Execute tasks per cGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing qualification block training program. Actively incorporate the Core Values set out by Emergent BioSolutions while performing day to day activities. Maintain state of facility environmental control including: preparation of defined concentrations of cleaning solutions, daily, monthly, quarterly and annual cleaning of manufacturing surfaces and equipment per Standard Operating Procedures. etc. | 5/31/2019 |
| 15223 | Emergent BioSolutions Gaithersburg, MD Associate Engineer, Process Development BS in engineering Exp: EIT certificate and/or 1-2 years related experience |
Under the direction of Process Development management, the Associate Engineer will perform experiments (hands-on) to develop, scale-up, and improve the performance of unit operations. The Assoc. Eng. will apply technical training to assess risks, solve problems, and analyze data sets coming from experiments and present results. This includes: preparation of solutions/media, cell culturing and related processes, tubing assembly and sterilization, development studies, etc. | 5/31/2019 |
| 15224 | Emergent BioSolutions Baltimore, MD Analyst I, Validation BS in science or engineering Exp: 0-2 years |
The Analyst I position will design and prepare all protocols and reports related to novel and diverse validation activities. The candidate will focus on Equipment, Utilities, and Software Validation. Responsibilities include: Write and execute validation and re-validation protocols and reports, (IQ / OQ / PQ), for the validation of new and existing processes, equipment, systems, etc. Write summary reports, following good documentation practices. Use Kaye Validator, DataTrace dataloggers, and/or Veriteq dataloggers to perform mapping studies. Analyze statistical data to verify acceptable criteria. etc. | 5/31/2019 |
| 15225 | Emergent BioSolutions Lansing, MI Analyst II, Microbiology - 3rd Shift MS in pharmaceutical or biochemistry Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Emergent BioSolutions Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. | 5/31/2019 |
| 15226 | Endiotix Boston, MA Executive Assistant/Office Manager HS Diploma Exp: 1-5 years, entry level will be considered |
The right candidate must be organized and calm under pressure. Excellent communication skills are essential for this role for external interactions. This position requires a professional demeanor and a high level of discretion in regards to handling of confidential company information. Must enjoy a “start-up” atmosphere and be flexible, show initiative, good judgment and be willing to take on additional tasks and responsibilities as needed to achieve goals and deliverables. Must have strong knowledge of Microsoft Office (Outlook, Excel, Word, PowerPoint) | 5/31/2019 |
| 15227 | Endo Pharmaceuticals Horsham, PA QC Analyst I - Microbiology BS in biological sciences Exp: 0-3 years in pharma/biotech |
The QC Analyst I – Microbiology will perform microbiological testing, release of in-process, intermediates and finished products, and testing for validation purposes. This role completes appropriate documentation to support testing procedures including data capture forms, equipment logbooks, and inventory forms. Additionally, this role is responsible for assisting with the writing of standard operating procedures (SOPs) and revision of existing documentation. | 5/31/2019 |
| 15228 | Endo Pharmaceuticals Horsham, PA Manufacturing Associate I USP BS in biological sciences Exp: 0-3 years in pharma/biotech |
The Manufacturing Associate I – Fermentation works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture Collagenase Clostridium Histolyticum (CCH) bulk drug substance (BDS). This role is responsible for supporting necessary fermentation and production activities, including validation and development work as needed. | 5/31/2019 |
| 15229 | Endologix Irvine, CA Supplier Quality Engineer BS in engineering or related Exp: 0-4 years in medical devices |
Responsible for supporting the Supplier Quality program and supporting cross-functional departments to acquire highest quality materials from suppliers that meet the requirements while improving the cost of quality of parts, processes and products. Provides support in the development and maintenance of company’s Quality Systems. Day to day activities include; supplier auditing, SCAR management, Supplier NCMR investigations, Supplier file maintenance, Supplier metrics, ASL and ACL | 5/31/2019 |
| 15230 | Stryker Portage, MI Associate Quality Assurance Technician HS Diploma Exp: 1-2 years of assembly |
Under general supervision performs repetitive inspection tasks on assembled products using Standard Work Instructions and Device History Records (DHRs) while maintaining training certifications. Will work from written and/or verbal instructions while maintaining pace with production requirements. Will interact with internal customers to help resolve, inspection and/or components issues. etc. | 5/31/2019 |
| 15231 | Stryker Kalamazoo, MI Design Engineer BS in software/electrical engineering, or computer sciences Exp: 0-2 years, experience is a plus |
As part of this team, you will interface with cross functional team members both on a local and global scale. Be responsible for creation to manufacturing of your design, this will include modeling, prototyping, and proving your design through testing. Specifically, this team member will join the team working to enhance the surgical environment for healthcare providers. Design, develop, test, work on compliance, traceability, documentation and refinement of embedded and application level software for medical device electro-mechanical systems | 5/31/2019 |
| 15232 | Stryker Chicago, IL Associate OnSite Repair Specialist AS/AA Exp: 1-2 years in reprocessing or surgical instrumentation |
The Surgical Instrument Repair Excellence (SIRE) Apprenticeship Program is a two to three-year process that is monitored by the Department of Labor (DOL). The first 4 – 6 months of initial training will be based out of the Houston Training Center (HTC). After completion of the training at HTC you will be required to spend the remainder of the introductory 6 months with established field personnel at their home sites. Learn and become proficient in all aspects of handheld stainless steel instrument sharpening, repair and maintenance (Maintain an average score of 80% on all written and technical assessments). | 5/31/2019 |
| 15233 | Stryker Sacramento, CA ENT Sales Associate BS/BA Exp: 1-2 years of sales support |
This position is a sales support role responsible for assisting and achieving regional goals. Responsibilities included building strong customer relationships, utilizing product knowledge, and case coverage support. You will proctor physicians during their initial procedures to provide guidance, gather procedure data and provide customer feedback on the Company’s product to appropriate individuals. Travel is extensive with temporary relocation dependent on the company needs. | 5/31/2019 |
| 15234 | Stryker Portage, MI Quality Engineer - Electrical/Software BS/BA in eletrical/software engineering, computer sciences, or related Exp: 0-2 yeras |
As an Advanced Quality Engineer, you will support the development of one or more products from concept generation through production, having the unique opportunity to realize the entire product lifecycle. Specifically, you will: Partner with marketing and design to understand user needs and translate those into engineering specifications that constitute the basis of the design. Lead the development of a safety risk management strategy including implementation of risk controls. etc. | 5/31/2019 |
| 15235 | Stryker San Jose, CA Packaging Test Engineer BS in packaging engineering/sciences Exp: 1-3 years in packaging/test engineering |
Test Engineers work closely with R&D to experiment with early prototypes and vet out product designs throughout the design process. Manages, improves, and maintains sterile and non-sterile packaging validations and associated procedures within Total Endoscopy. Maintains internal packaging validation work instructions are compliant and comprehensive per industry accepted procedures. etc. | 5/31/2019 |
| 15236 | CTI Covington, KY Clinical Research Associate BS in health fields Exp: 1+ years in clinical research monitoring |
The Clinical Research Associate completes project activities associated with monitoring functions of phase I through phase IV clinical research studies while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) / Good Clinical Practice (GCP) and applicable local regulations; provides clinical and technical support for CRAs and administrative staff; and performs management of study site activities to ensure integrity of clinical data in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs). | 5/26/2019 |
| 15237 | LivaNova Houston, TX Entry-Level Electrical Engineers BS/BA in electrical engineering Exp: recent graduates |
We are looking for only the most driven Electrical Engineers with solid engineering fundamentals. Responsibilities include: Circuit simulation/modeling, Bench data collection, Scripting & overall test automation, Chipset evaluations (e.g Bluetooth, MCUs, accelerometers…), PCB design & layout, etc. | 5/26/2019 |
| 15238 | Hologic San Diego, CA Oligo Process Development Chemist 1 BS Exp: 0-2 years |
Responsible for the manufacture of GMP oligonucleotides; the continuous improvement of these existing oligo processes; and the development/transfer of new oligo processes. Provides oligo process support to Operations group through instrument/oligo process troubleshooting and completion of NCR investigations. Responsible for research, development and production manufacturing activities associated with oligos. Responsibilities include: Independently produces notebook, dev, pilot and production materials per written directions, Analyzes in-process and final oligos using state of the art analytical techniques, Troubleshoots simple manufacturing process problems, etc. | 5/26/2019 |
| 15239 | Hologic San Diego, CA Process Development Associate 1 BS/BA Exp: 1+ years |
Responsible for the creation and transfer of manufacturing processes from R&D to Manufacturing and continuous improvement of existing processes. Responsibilties include: Maintains the Pilot Plant laboratory under cGMP conditions. Produces development, pilot and production materials per written instructions. Stocks and maintains the laboratory supplies. Completes laboratory work and associated paperwork by assigned completion dates | 5/26/2019 |
| 15240 | Hologic Methuen, MA Shipper 1 HS Diploma Exp: 1+ years in shipping/warehouse |
The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Responsible for picking, packaging, and preparing product for shipment. Assists in loading trucks and running end-of -day reports for carriers. Works with other members of the Distribution Team to ensure all orders are prepared and shipped daily. Runs packing lists and prepares finished goods for shipment. etc.The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Responsible for picking, packaging, and preparing product for shipment. Assists in loading trucks and running end-of -day reports for carriers. Works with other members of the Distribution Team to ensure all orders are prepared and shipped daily. Runs packing lists and prepares finished goods for shipment. etc.The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Responsible for picking, packaging, and preparing product for shipment. Assists in loading trucks and running end-of -day reports for carriers. Works with other members of the Distribution Team to ensure all orders are prepared and shipped daily. Runs packing lists and prepares finished goods for shipment. etc. | 5/26/2019 |
| 15241 | Hologic San Diego, CA Oligo Process Development Chemist 1 BS/BA or equivalent Exp: 0-2 years |
Responsible for the manufacture of GMP oligonucleotides; the continuous improvement of these existing oligo processes; and the development/transfer of new oligo processes. Provides oligo process support to Operations group through instrument/oligo process troubleshooting and completion of NCR investigations. Responsible for research, development and production manufacturing activities associated with oligos. Independently produces notebook, dev, pilot and production materials per written directions. | 5/26/2019 |
| 15242 | Hologic San Diego, CA Operations Test Associate BS/BA or equivalent Exp: 0-3 years lab experience |
We are currently seeking an Operations Test Associate responsible for generating accurate and reliable data for biologic products or medical devices on stability. Responsibilities include: Performs data analysis and results interpretations comparing to stability protocol defined specifications, validity criteria, and alert limits. Responsible for the maintenance and cleanliness of the laboratory, stocking shelves/drawers with testing materials. Responsible for the maintenance and cleanliness of equipment, calibrating or submitting items for calibration as needed. etc. | 5/26/2019 |
| 15243 | Hologic Malborough, MA Electrical Engineer I BS/BA in electrical engineering Exp: 1+ years |
The ideal candidate is one who understands complex electro-mechanical systems, and how they interact with software, manufacturing, service, and external vendors, to fulfill product requirements. This position would report to the Director of Research and Development. Designs and directs engineering personnel in fabrication of test control apparatus and equipment, and determines methods, procedures, and conditions for testing the engineered products and associated apparatus. Applied electrical engineering knowledge concerning the research, design and development of new products having state-of-the-art sophistication for X-ray generators, data acquisition, signal processing, power supplies, etc. | 5/26/2019 |
| 15244 | Evotec Watertown, MA Associate Scientist BS/BA in biology, chemistry, or related Exp: 1+ years in lab |
Cyprotex US, an Evotec Group, is looking for an Associate Scientist (Cell Biologist) based in Watertown, MA to assume responsibility for the routine screening of compounds in various in vitro ADME assays and reporting to the Associate Director or Senior Scientist. Responsibilities include: Design molecular or cellular laboratory experiments, oversee their execution, and interpret results. Conduct research on cell function, including mechanisms of gene expression, cell signaling, or cell differentiation. Compile and analyze molecular or cellular experimental data and adjust experimental designs as necessary. | 5/26/2019 |
| 15245 | Cytovance Biologics Okalahoma City, OK Manufacturing Sciences Technician BS in life sciences or related Exp: 1-3 years in GMP production |
The main responsibility of the Manufacturing Sciences technician is to support the manufacturing team as a technical advisor and operator. Manufacturing Sciences technicians adapt processes demonstrated at the R&D scale to final manufacturing scale. Secondary roles include driving/contributing to continual improvement initiatives and providing input to production scheduling | 5/26/2019 |
| 15246 | Decibel Theraputics Boston, MA Research Associate, Histology BS or MS in biological sciences Exp: 1+ year in lab |
The Research Associate will work closely with colleagues in platform development, biology, and pharmacology. In addition, the Research Associate will be responsible for restocking lab supplies and maintaining lab equipment. Core responsibilities include: Conduct whole body perfusion and collect tissue for histological analysis. Micro dissect and process inner ear tissues. Perform immunohistochemistry staining protocols. etc. | 5/26/2019 |
| 15247 | Deciphera Lawrence, KS Scientist - Biological Sciences BS or MS in biotechemistry Exp: 0-5 years |
This position will report to the Principal Investigator – Biological Sciences in the Lawrence, KS research facility. Key responsibilities include: Perform primary screening of small molecules utilizing cell-based assays. Primary responsibility will be in the area of screening small molecule kinase inhibitors. Perform routine mammalian cell culture. Together with supervisor, responsible for validating new biochemical or molecular biology-based assays and trouble-shooting when needed to establish reliable screening platforms. | 5/26/2019 |
| 15248 | Deciphera Lawrence, KS Scientist - Benzymology BS or MS in biotechemistry Exp: 0-5 years |
This position will report to the Senior Scientist – Enzymology in the Lawrence, KS research facility. Key responsibilities include: Perform routine drug screening assays for kinase inhibitors. Quality control of high throughput screening equipment. Together with supervisor, responsible for validating new biochemical assays and troubleshooting when needed to establish reliable screening platforms. Track and record data into corporate database and notebooks. Generate reports and create presentations as required by the organization. | 5/26/2019 |
| 15249 | Deciphera Waltham, MA Associate/Sr. Associate, Regulatory Affairs BS/BA or higher Exp: 1-3 years in clinical research or FDA regulation |
This position will report to the Sr. Manager, Regulatory Affairs and be located in the Waltham, MA office. Responsibilities include: Under supervision, the Regulatory Affairs Associate will work with cross functional colleagues in providing support for clinical and CMC regulatory filings, creation of internal regulatory documents, and assist with ensuring internal compliance with GXP regulations and policies. Define contributions for submissions, communicate to functional contributors and track delivery according to agreed timelines. Identify and compile all materials required in U.S., EU, and other ex-US regulatory submissions, this includes annual reports, DSURs for INDs, CTAs, IND/NDA/MAA applications, etc. as necessary | 5/26/2019 |
| 15250 | Dendreon Richmond, VA Immunotherapy Sales Specialist - Richmond, VA BS/BA in sciences/technical field Exp: 1+ year in biotech/medical device sales |
Dendreon’s Immunotherapy Sales Specialist is responsible for achieving sales objectives in an assigned territory through the development, maintenance, and enhancement of the business. Customers include oncologists, urologists, nurses, pharmacists, pharmacy and therapeutics groups, tumor boards, teaching institutions, hospitals and formulary committees. The role is responsible for ensuring customer’s clinical conviction in the product as well as guiding the customer through the logistics process and seeing the sale through to its conclusion. The territory alignment for this role is the state of Virginia. | 5/26/2019 |
| 15251 | Dexcom San Diego, CA Mechanical Engineer 1 BS/BA in technical discipline Exp: 0-2 years |
Under the direction of the Operations Mechanical Engineering Manager, the Mechanical Engineer provides technical support for the projects, functions, and strategic objectives of the Operations Mechanical Engineering department, focusing on: engineering support for new product development; development of fixtures and equipment as standalone and in support of automated systems; failure mode analysis and corrective action of process equipment and instruments; sustaining engineering for the legacy and newly deployed manufacturing systems; engineering and quality documentation development. | 5/26/2019 |
| 15252 | Dexcom San Diego, CA Quality Assurance Analyst 1 BS/BA in technical discipline Exp: 0-2 years |
Supports the organization with initial compliance and ongoing preparation, testing and monitoring of conformance to established quality assurance processes and standards for manufacturing and production. Performs evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards. Identifies risk and evaluates deficiencies while working with internal departments/business units to appropriately remedy them. Facilitates internal training on quality assurance requirements, processes, and procedures. May perform audits and risk assessments. | 5/26/2019 |
| 15253 | Dexcom San Diego, CA Engineering Technician 1 HS Diploma or AA/AS Exp: 1-2 years in production equipment operations |
Responsible for preventative and reparative maintenance of the equipment, process and/or electronics located in the Production and R&D Departments. Prepares and maintains appropriate documents in RAM, Agile and Track-It. Helps with Process and Equipment Validations, IQ's and OQ's and process protocals. Equipment project work and validations assigned as needed. Follows Good Manufacturing Protocals. | 5/26/2019 |
| 15254 | Dexcom San Diego, CA Clinical Data Associate MS in technical dicipline Exp: 0-2 years |
Collaborates with various departments on the design, documentation, testing and implementation of clinical data studies. Develops systems for organizing data to analyze, identify and report trends. Analyzes the interrelationships of data and defines logical aspects of data sets. Prepares reports of clinical trial studies for internal validation and cross validation studies. May evaluate and resolve issues regarding contents of reports. | 5/26/2019 |
| 15255 | Dexcom San Diego, CA Research Associate 1 BS/BA in technical discipline Exp: 0-2 years |
Performs research and/or development in collaboration with others to complete science-based projects. Makes detailed observations, analyzes data and interprets results. Investigates, creates and develops new methods and technologies for project advancement. Maintains high level of professional expertise through familiarity with scientific literature. May participate in scientific conferences and contribute to scientific journals. May be responsible for identifying patentable inventions. May act as principal investigator in conducting own experiments. | 5/26/2019 |
| 15256 | Dexcom San Diego, CA Mechanical Engineer 1 BS/BA in technical discipline Exp: 0-2 years |
Under the direction of the Operations Mechanical Engineering Manager, the Mechanical Engineer provides technical support for the projects, functions, and strategic objectives of the Operations Mechanical Engineering department, focusing on: engineering support for new product development; development of fixtures and equipment as standalone and in support of automated systems; failure mode analysis and corrective action of process equipment and instruments; sustaining engineering for the legacy and newly deployed manufacturing systems; engineering and quality documentation development. | 5/26/2019 |
| 15257 | Dexcom San Diego, CA Quality - Quality Assurance Analyst 1 BS/BA in technical discipline Exp: 0-2 years |
Supports the organization with initial compliance and ongoing preparation, testing and monitoring of conformance to established quality assurance processes and standards for manufacturing and production. Performs evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards. Identifies risk and evaluates deficiencies while working with internal departments/business units to appropriately remedy them. Facilitates internal training on quality assurance requirements, processes, and procedures. May perform audits and risk assessments. | 5/26/2019 |
| 15258 | DiCE Molecules Redwood City, CA Research Associate - Assay Science (Biology) BS or MS in biochemistry, molecular biology, or related Exp: 0-4 years in biotech |
Responsibilities to include: Performing key assays to support drug discovery using biochemistry, cell biology and/or biophysics. Generating high-quality, reproducible data by leveraging liquid handling, laboratory robotics and advanced data analysis tools. Identifying and developing new assays as the project requires. Communicating experimental results to project teams. | 5/26/2019 |
| 15259 | Dicerna Pharmaceuticals Cambridge, MA Research Associate/Associate Scientist, RNAi Pharmacology BS or MS in biochemistry, molecular biology, or related Exp: 1+ years |
Key responsibilities include: Rodent dosing, sampling and necropsy; planning and performing of all technical aspects of in vivo experiments; contributing to experimental design and strategy. Cross-functional collaboration to help enable efficient operation of our on-site animal care facility (ACF). Performing laboratory assays according to SOPs, troubleshooting as needed; assay development. Generating data using both standard and novel molecular technologies. Contributing to a team tasked with evaluating novel experimental medicines in preclinical models of disease, and advancing our technology to enable development of the next generation of innovative RNA-based therapeutics. | 5/26/2019 |
| 15260 | Dicerna Pharmaceuticals Cambridge, MA Research Associate/Associate Scientist, RNAi Discovery BS or MS in relevant field Exp: 0-5 years |
Dicerna Pharmaceuticals is looking for a BS/MS scientist to help in its drug discovery efforts. This is a hands-on research position that requires strong expertise in molecular and cellular methodologies. Key responsibilities include: siRNA drug candidate screening, hit identification, and lead optimization. In vivo drug candidate testing (e.g. mouse dosing; sample analysis) | 5/26/2019 |
| 15261 | DMS Health Technologies Wausau, WI Medical Assistant (Technologist Assistant) HS Diploma Exp: 0-1 year |
The technologist assistant assists the technologist with patient care by transporting patients between the facility and scanner; sanitizing and cleaning patient care and staff areas; changing table linens; entering exam and patient information electronically or on paper; and answering the telephone. The technologist assistant demonstrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. The individual demonstrates knowledge of the principles of growth and development over the life span. He/she is able to identify and categorize each patient’s age-specific grouping of needs, such as those for infant, pediatric, adolescent, adult or geriatric patients. | 5/26/2019 |
| 15262 | DMS Health Technologies Santa Maria, CA Medical Assistant PRN HS Diploma Exp: 0-1 year |
The technologist assistant assists the technologist with patient care by transporting patients between the facility and scanner; sanitizing and cleaning patient care and staff areas; changing table linens; entering exam and patient information electronically or on paper; and answering the telephone. The technologist assistant demonstrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. The individual demonstrates knowledge of the principles of growth and development over the life span. He/she is able to identify and categorize each patient’s age-specific grouping of needs, such as those for infant, pediatric, adolescent, adult or geriatric patients. | 5/26/2019 |
| 15263 | DMS Health Technologies Minneapolis, MN Medical Assistant HS Diploma Exp: 0-1 year |
The technologist assistant assists the technologist with patient care by transporting patients between the facility and scanner; sanitizing and cleaning patient care and staff areas; changing table linens; entering exam and patient information electronically or on paper; and answering the telephone. The technologist assistant demonstrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. The individual demonstrates knowledge of the principles of growth and development over the life span. He/she is able to identify and categorize each patient’s age-specific grouping of needs, such as those for infant, pediatric, adolescent, adult or geriatric patients. | 5/26/2019 |
| 15264 | DMS Health Technologies Glen Burnie, MD Cardiac Stress Tech AS or BS/BA Exp: 1+ years in emergency care setting |
Under the direct supervision of the site physician, performs various professional and administrative duties related to nuclear medicine stress testing including but not limited to: patient preparation-including IV start and EKG lead placement interpretation, administration of exercise and pharmacological stress tests, and application of ACLS measures to patients when directed. Activities not performed at the physician site are supervised by the Area Supervisors and Business Directors. | 5/26/2019 |
| 15265 | DJO Vista, CA Maintenance Technician 1 HS Diploma Exp: 1+ years |
Performs basic and routine functions associated with the maintenance or repair of the manufacturing process including machines and equipment. Utilizes fundamental knowledge of a select number of machines, equipment and manufacturing processes to perform duties that may include but are not limited to: performing electronic, electrical or mechanical troubleshooting to determine problems in non-functioning equipment or machinery used in the manufacturing process; dismantling, adjusting, repairing and assembling equipment and machinery according to layout plans, blueprints, operating or repair manuals, rough sketches or drawings; using test and diagnostic equipment to perform checkouts; rebuilding or modifying manufacturing equipment as required. May troubleshoot software as it pertains to test equipment or machinery as needed. | 5/26/2019 |
| 15266 | DJO Vista, CA Product Assembler HS Diploma Exp: 1+ years |
Utilizes a developing to full understanding of operational processes and procedures to perform an assortment of assembly activities of moderate scope on a mixture of products, components, assemblies or sub assemblies. Follows methods, and sequence of operations according to specifications, blue prints and bills of materials. Ensures quality and product conformance. Sets up assembly for production. Performs various tasks which may include but is not limited to: wiring, component installation, hand soldering, cable harnessing, welding, painting, milling, filling, sewing, templating and fitting on assembly units. Performs maintenance responsibilities as needed and keeps surrounding area clean, safe and organized. Develops and recommends new methods to improve processes. Follows and complies with Company policies, standards and practices. | 5/26/2019 |
| 15267 | Dragonfly Therapeutics Waltham, MA Laboratory Operations Coordinator BS/BA in natural sciences Exp: 1+ years |
Dragonfly Therapeutics seeks an experienced and motivated Laboratory Operations Coordinator to help supportnovel cancer immunotherapy programs. The candidate must be independent, goal-oriented, flexible, and able to work efficiently in a laboratory environment as well as an office setting. Responsibilities include: Monitor day to day lab operations and support equipment maintenance, stock lab consumables, and collect asset and maintenance data. Provide office operational support to colleagues, partners, and ongoing research collaborators by helping with procurement, researching supply issues, and providing supply options. Create, manage, and participate laboratory and office protocols such as safety procedures, lab emergency response, and communicating general lab rules and company policies. | 5/26/2019 |
| 15268 | Dynosense San Jose, CA QA Engineer BS in computer science, eletrical engineering or related Exp: 0-2 years |
Job duties include: Estimate, plan, and coordinate testing activities. Develop test plan, test cases, test scenarios based on Users Stories and product’s design description to meet business requirements and technical specifications. Perform ad hoc, functional, integration, and regression testing. Identify software defects and submit problem reports via bug-tracking system. Perform regression testing on fixed issues. | 5/26/2019 |
| 15269 | Editas Cambridge, MA Research Associate, Cellular Process Development BS/BA in life sciences Exp: 1+ years |
This individual will also assist in the development and execution of isolation and cryopreservation procedures for various cell types (PBMCs, T cells, CD34+, etc.). Candidate must be experienced with aseptic technique and be versatile to assist in the development and execution of processes for normal donor cellular products derived from different lineages of cells. Candidate must be experienced with aseptic technique and be versatile to assist in the development of processes for autologous or normal donor cellular products derived from different lineages of cells (T cells, HSCs, etc.). | 5/26/2019 |
| 15270 | Editas Cambridge, MA Research Associate I/II, Screening BS or MS in cell biology or related Exp: 1-3 years lab experience |
Editas is seeking a highly motivated Research Associate I/II to join our Screening Team. In this role, you will contribute to the pre-clinal development of gene-edited cell products. An ideal candidate should have a strong background in cell and molecular biology. Demonstrated culture experience with both IPSC or primary cell lines and a strong interest in genome editing. Experience and interest with lab automation and liquid handling robots, Biomek Fx / I7 or similar, is a plus. | 5/26/2019 |
| 15271 | Editas Cambridge, MA Research Associate I/II, Immunotherapy BS or MS in, immunology, biology or related Exp: 1-3 years lab experience |
An ideal candidate should have a background in immunology, cancer biology, and a strong interest in genome editing. Responsibilities include: Develop and optimize protocols for gene editing, including: delivery methods, culture conditions, scale up, and multiplexing. Culture primary cells and cell lines. Perform basic molecular biology work such as DNA and RNA extraction and PCR. Develop and perform immune cell activation, cytotoxicity, and other cellular and ELISA-based assays to evaluate gene editing approaches in cell therapeutics in vitro and in vivo. etc | 5/26/2019 |
| 15272 | Codexis Redwood City, CA Research Assistant, Molecular Biology BS in molecular biology or related Exp: 0-2 years |
Responsibilities include: Construction of gene libraries and expression vectors. Characterization of gene variants. Primer design. DNA isolation. DNA sequencing. Cloning of genes and genetic pathways. Work with project teams to provide support and assistance to all phases of directed evolution projects, contribute to team presentations and written reports. | 5/25/2019 |
| 15273 | Codexis Redwood City, CA Research Assistant (Biochemistry) BS in molecular biology or related Exp: 0-2 years |
We are looking for an entry level Research Assistant interested in analytical method development and protein biochemistry. Successful candidates will be part of an interdisciplinary, dynamic and enthusiastic protein engineering team responsible for implementing Codexis’ core technologies and delivering commercially-relevant and highly-evolved proteins. Responsibilities include; Assist in developing relevant enzyme assays in HTP format. Grow cultures, express proteins, and test enzyme activity in high throughput and in larger scales. Analyze HTP samples in HPLC, UV-Vis Spectrophotometry, GC, LC-MS, or GC-MS to identify and quantify small-molecule products. | 5/25/2019 |
| 15274 | Codiak Cambridge, MA Associate Scientist II Protein Sciences MS in biology, chemistry or related Exp: 1+ years research experience |
Codiak is seeking a qualified associate scientist to join our growing Research organization and contribute to the development of the company’s innovative exosome engineering platform. Responsibilities include: Produce, purify, and characterize engineered exosomes from conditioned cell culture medium; Execute biochemical and cell-based assays to validate target and pathway engagement of therapeutic candidates; Express and purify recombinant proteins, including antibodies, enzymes, and fusion proteins, at the milligram scale to support assay development for ongoing projects;etc. | 5/25/2019 |
| 15275 | Cogent Terre Haute, IN Laboratory Technician HS Diploma Exp: 1+ years pharma lab experience |
The Laboratory Technician ensures the quality of products by developing, validating and documenting analytical methods and performing physical and chemical analyses of raw materials, in-process and finished products in support of the manufacturing process. Perform test sample extractions or dilutions and execute instrumental analysis using high performance liquid chromatography (HPLC). Perform other laboratory testing as required, including but not limited to, GC, LOD, Ash, and particle size analysis (sieve method). etc. | 5/25/2019 |
| 15276 | Cogmedix Westborough, MA Electrical Engineer I BS in electrical engineering Exp: 0-5 years |
As a member of the engineering services team, the Electrical Engineer I will solve complex problems and participate in the specification, design, prototyping and testing of a diverse range of tooling, fixtures, design for manufacturability projects, and other customer product design needs. Under the direction of the Electrical Engineering Manager, the engineer in this role will be performing design tasks of a complex technical nature requiring investigation of new technologies, and applying engineering design principles and practices. | 5/25/2019 |
| 15277 | Coloplast Mankato, MN QA Chemist BS in chemistry or related Exp: 0-5 years |
As a QA Chemist, you will be is responsible for performing inspections and tests on raw materials, in-process products, bulk products, finished goods and stability samples to ensure conformance to established specifications. Perform in-process inspections and determine any adjustments required. Perform bulk and finished product inspections, testing and analyses. Confirm samples meet established standards and specifications and release items as appropriate. Develop and validate analytical methods based on USP requirements and local needs and available instrumentation. Record test data and results using standard laboratory data calculations. Verify notebook entries and calculations for lab staff. Assure equipment is calibrated prior to use and complete preventative maintenance. etc. | 5/25/2019 |
| 15278 | Complete Genomics Montreal , Ca Lab Technician BS in molecular biology or related Exp: 1-2 years |
The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. Execute on and assist in the development of process instructions that ensure accuracy, throughput, and quality. Operate and monitor laboratory automation and instrumentation. Communicate issues and failures as necessary to the appropriate parties. General lab duties, such as restocking supplies and maintaining inventory. | 5/25/2019 |
| 15279 | Complete Genomics San Jose, CA Lab Technician BS in molecular biology or related Exp: 1-2 years |
The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. Execute on and assist in the development of process instructions that ensure accuracy, throughput, and quality. Operate and monitor laboratory automation and instrumentation. Communicate issues and failures as necessary to the appropriate parties. General lab duties, such as restocking supplies and maintaining inventory. | 5/25/2019 |
| 15280 | Conformis Billerica, MA Design Engineer I BS in mechanical or biomedical engineering Exp: 1-2 years |
The Design Engineer I will be responsible for design and development of new orthopedic implants and related instrumentation systems and the creation of documentation in support of quality systems and concept to medical device which achieve quality, cost and time to market requirements. Understand the objectives, responsibilities, and mission of the Engineering department and works towards those goals. Develop protocols for design verification and validation (V&V), including outside test and research labs. Complete corresponding test reports. Communicate with customers, sales, marketing and independent entities to gain knowledge of product design requirements. | 5/25/2019 |
| 15281 | Conformis Billerica, MA Hip Cell Programming, 1st Shift HS Diploma Exp: 1-3 years |
This position is responsible for operation of Pre/Post machining from start to finish for hip stem and hip acetabular Cups. Responsibilities include: Printing DHR’s for production release of hip stem and acetabular cup . Programming of acetabular cup and hip stem . CNC operation of acetabular cup and hip stem . Comply with all company policies and procedures including safety regulations, personal protective equipment requirements, Standard Operating Procedures, Work Instructions and Good Manufacturing Procedures | 5/25/2019 |
| 15282 | ConMed Utica, NY Pricing Analyst I BS in business or finance Exp: 1-3 years |
Supports management, sales, marketing, contracts, and other administrative areas by providing timely and accurate financial projections, price quotations, contracts, and profit analyses. Performs financial analyses, including forecasts, projections, and historical assessments. Produces quotes for capital and/or disposables not covered by existing contracts. Facilitates communication among management, sales, and contracts staffs regarding contract and price. | 5/25/2019 |
| 15283 | ConMed Largo, FL Machining Associate HS Diploma Exp: 1+ years |
Purpose: Produce parts that meet requirements using a variety of manual and/or automated equipment through established procedures. Accurately perform basic metrology tasks utilizing basic measurement devices such as calipers, micrometers, etc. Set-up and operate various manual and automated production machines where set-up is well defined and operate simple CNC type machines that are already set-up for production. Must be willing and able to continually rotate through a variety of manufacturing processes and duties, performing all types of tasks in a cell/team environment. | 5/25/2019 |
| 15284 | ConMed Largo, FL Quality Engineer I - New Product Development BS in related field Exp: 0-3 years medical device experience |
The Quality Engineer New Product Development (NPD) is responsible for supporting all quality engineering activities to support the new product life cycle, from concept through commercialization and sustaining changes, as part of a cross-functional development team. Serves as the key resource for ensuring compliance to ISO, MDD and QSR requirements for Medical Devices. Takes the lead with quality initiatives with inter-organizational impact following QSR, ConMed Policies and standards. Works under direction from Quality Management. | 5/25/2019 |
| 15285 | ConMed Utica, NY R&D Engineer I BS in electrical or biomedical engineering Exp: 0-2 years |
e are seeking a R&D Engineer I to join the Cardiology and Critical Care R&D team, based in Utica, NY, to work on new product development and sustaining engineering activities for this product portfolio. This engineer will have immediate opportunities to contribute in a fast paced and hands on environment. Support the development of new and existing product specifications and requirements based on design input requirements, in collaboration with the project engineer. Write technical reports, risk management documents, VOC summaries, test protocols and design input and output documents. Perform sustaining engineering activities including problem troubleshooting, root cause analysis, investigations, and resolving part obsolescence issues | 5/25/2019 |
| 15286 | ConMed Denver , CO Mechanical Engineer I BS in electrical, mechanical, or biomedical engineering Exp: 0-3 years engineering experience |
The Mechanical Engineer will work with a cross-functional teams on new product development and sustaining engineering activities. Support the development of new and existing product specifications and requirements based on design input requirements, in collaboration with the project engineer. Supports the writing of technical reports, risk management documents, VOC summaries, test protocols and design input and output documents. Create detailed 3D CAD models and drawings of mechanical and electrical parts and assemblies | 5/25/2019 |
| 15287 | Cook Bloomington, IN Quality Engineer BS in sciences/engineering Exp: 0-2 years |
The Quality Engineer at Cook Medical is responsible for executing and/or monitoring key processes in support of the Quality Management System: auditing; complaint investigation; corrective and preventive action (CAPA); control of non-conformances; document, data, and change control; process control; risk management and supplier quality management. The Quality Engineer fulfills the role of Independent Reviewer of many key process outputs | 5/25/2019 |
| 15288 | Cook Pittsburgh, PA Quality Control Microbiology Assistant AS degree in life sceicenes Exp: 1-3 years in lab/GMP environment |
The Quality Control Microbiology Assistant at Cook MyoSite will assist GMP testing and perform environmental monitoring activities to support lot release and in-process testing. Preparation of equipment and instrumentation for further use in analytical assay and/or microbiological testing. Perform environmental monitoring activities such as collecting viable air, surface EM samples, non-viable particulate samples, and reading of EM plates. Support to maintain cleanroom environment below alert limits by participating in and following established cleaning practices and cleanroom behavior | 5/25/2019 |
| 15289 | Cook Spencer, IN Regulatory Engineer BS/BA in engineering or sciences Exp: 0-4 years |
The Regulatory Engineer provides technical support to Regulatory Affairs for the development of regulatory documentation for compliance with FDA and international regulatory requirements. Develop new, and refine existing, systems that provide the necessary information for successful submission to global regulatory bodies . Assist various Regulatory Affairs staff with technical assessment and writing of regulatory submissions and responses to regulatory agencies. Prepare regulatory submissions for new products, product changes, and re-registrations, as required. etc | 5/25/2019 |
| 15290 | Cook Bloomington, IN Research and Development Packaging Engineer MS in packaging sciences Exp: 0-3 years |
The Packaging Engineer II procures and develops packaging for new and existing products. A Packaging Engineer II leads packaging activities with a cross-functional team including SBU Product Management, Regulatory Affairs, Operations, Quality Assurance, Clinical Affairs, and other Engineering personnel. | 5/25/2019 |
| 15291 | Cook Winston-Salem, NC Regulatory Affairs Specialist I BS/BA in related field Exp: 0-2 years |
The Regulatory Affairs Specialist I is responsible for the planning and preparation of submissions to obtain regulatory approvals for new and modified Class I, II, III and IV medical devices in specific markets. In addition to submissions, the Regulatory Affairs Specialist will serve as a communication liaison between the Cook manufacturer and the Cook Local Office / Cook Distributor. | 5/25/2019 |
| 15292 | Cook Winston-Salem, NC Quality Engineer - Post Market BS/BA in related field Exp: 0-2 years |
The primary purpose of the Quality Engineer (Post Market) position at Cook Winston-Salem is complete and review post market quality engineering activities, including complaint investigations, risk assessment, post market feedback, and product quality issues. Responsibilities include: Perform complaint investigations, including technical assessment of returned products. Complete risk assessments using post market data. Assist with the investigation, risk assessment and resolution of product quality and quality system issues. Implement, support and maintain post-production quality activities. | 5/25/2019 |
| 15293 | CryoLife Austin, TX Component Processing Technician - Final Assembly HS Diploma Exp: 1-4 years in manufacturing |
Position Overview: Perform work station assembly operations including sewing and packaging of heart valves in a clean room. Inspect incomplete and finished components for conformance to written specification with the aid of a microscope, and follow standard work methods and practice safe work habits to ensure production is as efficient and safe as possible. | 5/25/2019 |
| 15294 | CSL Kankakee, IL QAO Specialist I BS/BA in sciences/technical field Exp: 0-2 years in cGMP environment |
Provide an overview of the responsibilities of the position by providing a summary of the most important aspects and duties of the position. This is an entry level position into Quality Assurance Operations. Developing responsibilities include assisting with investigating deviations, relevant to area of responsibility. Responsible for driving continuous improvement on production floor to ensure compliance to cGMPs. Real time review of batch records, including critical processing steps with production floor presence. | 5/25/2019 |
| 15295 | CSL Holly Springs, CN Associate I/II/III, Manufacturing (Upstream) Night Shift HS Diploma or BS/BA Exp: HS: 1+ years, BS: 0 years |
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (be trained in) the technical skill-sets necessary to manufacture high quality biologicals or sterile injectables safely in a compliant, efficient, and cost effective manner. Responsibilities include; Becomes trained on basic processes and equipment and serves as a hands-on resource in Production. Cleaning, preparing, and sterilizing production equipment. Assembly, set-up, and disassembly of production equipment. Handling biologically and chemically hazardous goods | 5/25/2019 |
| 15296 | BioPharmGuy Anytown, US Contract Data Confirmation Some college Exp: 0 years |
Looking for a contract worker to confirm contacts we have on file. Job mostly involves searching on LinkedIn and company websites. Must be able to accept payment via PayPal. Must be eligible to work for any U.S. Employer. Send a message through our contact form. | 5/20/2019 |
| 15297 | Charles River Wilmington, MA Lab Technician I BS in biological sciences Exp: 0-2 years |
Performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Perform within the Bacteriology laboratory process internal and external rodent samples by for microbiological identification. Reconcile customer paperwork with submission documentation to ensure accuracy. Make detailed observations and maintain documentation of all laboratory work. Comply with all Standard Operating rocedures (SOPs) and operating equipment and hazardous and non-hazardous chemicals and biological material according to laboratory safety policy | 5/19/2019 |
| 15298 | Charles River Reno, NV Necropsy Technician I HS Diploma/GED Exp: 1+ years in pathology lab |
Perform basic necropsy laboratory procedures. Participate in the documentation of all activities as required. Receive and ship samples. Assist with and perform basic necropsy procedures (basic dissection, tissue collection/preservation, fresh tissue trimming, sample collection, etc.). Learn/know correct anatomic terms. Receive samples, complete tracking documentation, and prepare pathology materials and data for shipment and archiving | 5/19/2019 |
| 15299 | Charles River Mattawan, MI Quality Assurance Auditor 1 BS/BA in life scienes Exp: 1-2 years in QA GLP role |
The following are responsibilities related to the Quality Assurance Auditor 1: A Quality Assurance (QA) Auditor I is responsible for performing audits of basic records and reports and inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures. | 5/19/2019 |
| 15300 | Charles River Ashland, OH Research Technician I, Inhalation HS Diploma/GED Exp: 0.5-1 years in animal lab |
We are seeking a Research Technician I for our Safety Assessment Group site located in Ashland, Ohio. Collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 5/19/2019 |
| 15301 | Charles River Kingston, NY Technician I HS Diploma/GED Exp: 0.5-1 years in animal lab |
The Technician I will perform routine animal husbandry and other production duties, and maintain supplies and environment of environmentally-controlled work area(s). Other essential duties and responsibilities include: Perform routine animal husbandry duties and monitor daily health and welfare to maintain quality and health of animals. Handle, transfer, and distribute animals, supplies and waste as needed to and from work area(s). Perform physical environment housekeeping duties and production operations according to Good Manufacturing Practices (cGMPs) and/or Standard Operating Procedures (SOPs). Maintain recordkeeping pertaining to equipment operation, animal or supply area inventories. | 5/19/2019 |
| 15302 | Charles River Shrewsbury, MA Lab Operations Technician I BS/BA in sciences Exp: 1-3 years lab experience |
In this position, the Laboratory Operations Technician I will be responsible for performing a variety of tasks involved in sample receiving and processing, and inventory management of critical components, laboratory supplies, specialty reagents, and client-supplied reagents and controls. Perform activities related to sample log in, processing, storage, shipping of materials client support, laboratory and facilities order placement, and order tracking, receiving, and processing. | 5/19/2019 |
| 15303 | Charles River Reno, NV Research Assistant I (Formulations) BS/BA in sciences Exp: 0-2 years in biology/chem/pharma labs |
This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 5/19/2019 |
| 15304 | EyeCRO Ann Arbor, MI Research Assistant - Chemistry BS/BA in chemistry or chemical engineering or related Exp: 1+ years as research technician |
This person will be responsible for participating in a wide variety of lab-based activities inlcuding: Routine wet chemistry. Operation of various analytical instruments (HPLC, LC/MS, and liquid handlers). Animal handling/husbandry. Animal procedures. Record keeping. etc. | 5/19/2019 |
| 15305 | ChemBio Medford, NY Regulatory Affairs Associate BS or MS in life sciences Exp: 0-3 years in FDA regulated industry |
Primarily to assist in the regulatory filings of new products as 510(k), PMA and / or BLA submissions for in-vitro diagnostic devices as well as post approval related regulatory filings for the lawful marketing of Chembio products. Review change control process as it pertains to reportable changes to FDA CBER and CDRH. Assist in 180-day supplements and clinical filings to regulatory agencies etc. | 5/19/2019 |
| 15306 | CHeminPharma Branford, CT Associate Scientist, Medicinal/Synthetic chemistry BS or MS in synthetic chemistry Exp: 0-5 years in lab setting |
The successful candidate will be an experienced chemist with state of the art knowledge of synthetic organic chemistry and will be a motivated, creative, hands-on laboratory scientist with the ability to interact effectively with team members and external customers. Major responsibilities will involve design, synthesis, purification, and characterization of novel chemical entities and the management of general chemistry lab operations under the direction of senior scientific staff. The qualified individual is expected to contribute to process development and scale-up of key intermediates. | 5/19/2019 |
| 15307 | ChemPacific Baltimore , MD Chemist MS in chemistry or organic chemistry Exp: 1+ years |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 5/19/2019 |
| 15308 | CliniLabs na, TX Clinical Research Associate (CRA) – Texas BS in life sciences or nursing degree Exp: 1+ year as clinical mentor |
The Clinical Research Associate (CRA) monitors activities at clinical trials sites to assure adherence to Good Clinical Practices (GCP), standard operating procedures, and study protocols. The CRA reviews regulatory documents as necessary, and prepares site visit reports. The person in this position is involved in the selection of potential clinical investigators and determines if facilities are adequate based on protocol requirements. | 5/19/2019 |
| 15309 | Clovis Oncology San Francisco, CA Clinical Research Associate BS/BA in sciences or health Exp: 1-2 years clincal research experience |
Assist in managing all aspects of clinical trials to ensure that studies are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines. Assist with the management of key study parameters (e.g. start-up activities, enrollment, site management, data collection, data reviews, site feasibility, database lock, etc.) and proactively identify solutions within the clinical team when issues arise. Develop and review informed consent forms, case report forms, study manuals, and other clinical trial materials. Assist in the evaluation and management of CROs and other vendors and systems. Negotiate and manage contracts/budgets with CROs and other vendors. | 5/19/2019 |
| 15310 | Clovis Oncology San Francisco, CA Clinical Trial Assistant BS/BA in sciences or health Exp: 1-2 years clincal research experience |
The Clinical Trial Assistant provides support to the clinical operations department to assist with execution and maintenance of clinical studies. Acts as a central support for the clinical team for designated project communications, correspondence, and associated documentation. Maintains, updates, and may establish various databases for clinical activity tracking. Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites. | 5/19/2019 |
| 15311 | Cochlear Centennial, CO Insurance Verification Specialist HS Diploma/GED Exp: 1-2 years customer service |
In order to support cochlear implant clinics and recipients, we are recruiting for an Insurance Verification Specialist. To be successful in this role, you will facilitate all pre-claim activity for reimbursement orders while providing exceptional service to internal and external customers. You will act with a sense of urgency to address inquiries while demonstrating a high degree of knowledge, integrity, and empathy in all aspects of team performance and operations. | 5/19/2019 |
| 15312 | ImmunoSpot Cleveland, OH Laboratory Assistant BS Exp: 1+ years in GLP/GCP lab |
We are seeking a Laboratory Assistant for our Contract Research Laboratory who will perform immunology testing of client specimens collected from both pre-clinical and clinical studies using the following test methods: ELISPOT, ELISA, flow cytometry, etc. You will help support our quality improvement projects in conjunction with QA, support our quality system by data quality control, communicate with fellow laboratory personnel, maintain laboratory equipment, write reports, etc. All work is performed according to general laboratory safety standards, internal standard operating procedures (SOPs), client protocols, and applicable international, federal and state regulations. | 5/17/2019 |
| 15313 | Cepheid Sunnyvale, CA Manufacturing Associate II HS Diploma/GED Exp: 1-2 years |
Responsibilities as a manufacturing associate include: Follow documentation procedure (filling out Data History Records (DHRs), reading and understanding instructions from Work Release (WR), Planned Deviation Report (PDR) or Non-Conformance Report (NCR). Read and follow Standard Operating Procedures (SOPs) and Manufacturing Work Instructions. Maintain dry room and cleanroom standards, practices, and housekeeping according to standard operating procedures. Set up and operate manufacturing equipment. Monitor machines and inform Supervisor and/or Lead of problems. Clean and maintain equipment and work area as needed. | 5/17/2019 |
| 15314 | Cepheid Sunnyvale, CA Reagent Manufacturing Technician HS Diploma/GED Exp: 1-2 years |
The position will be working in a chemical lab that manufactures liquid reagents in bulk quantities. Responsible for the overall operation of the bulk lab throughout the shift and ensure that all activities are compliant with the company’s Quality, Safety and departmental policies and standards. Essential functions include: Formulate bulk liquid reagents following standard operating procedures. Work safely with hazardous chemicals and follow all Safety policies to ensure zero incidents in the lab. Recommend or suggest improvement ideas in the lab that will positively affect production efficiency, Quality and Safety compliance | 5/17/2019 |
| 15315 | Cepheid Sunnyvale, CA Software Engineer BS/BA Exp: 0-2 years |
Cepheid is looking for a Software Engineer to join our product software team developing molecular diagnostics applications using Java and Angular predominantly. You will be a member of the software team responsible for designing, developing, testing, and implementation of Cepheid next generation software products. Repsonbilities include: Design, develop, troubleshoot and debug software products using Java and Angular. Maintain robust software applications by participating in software debugging and testing. Adhere to software development and source control processes. | 5/17/2019 |
| 15316 | Synchorgenix Philadelphia, PA Regulatory Submission Specialist BS/BA Exp: 0-3 years |
The Regulatory Submissions Specialist will serve as a team member for electronic submission publishing (primarily eCTD format) and SPL conversion projects. He/she will collaborate with the Synchrogenix team and interact with clients on routine project related correspondences. The Regulatory Submissions Specialist will be responsible for completing publishing tasks that are assigned in order to meet submission deadlines. Prepare, compile, scan, render, and maintain regulatory submissions to Regulatory Health Authorities and other government agencies worldwide. Publish documents by creating bookmarks and hyperlinks into submission files according to Synchrogenix and client policies. | 5/17/2019 |
| 15317 | Ceva Lenexa, KS Live TCO/CEO Lab Technician I AS/AA or BS/bA in life sciences Exp: AS: 1-2 years, BS: 0 years |
The Manufacturing Lab Technician I will work directly with Viral seed culture and Virus propagation techniques, prepare buffer/media solutions and equipment preparations, and inactivation methods following aseptic technique and cGMP procedures. Operators will be in a full gowned environment and will be need to use strict aseptic techniques. | 5/17/2019 |
| 15318 | Champions Oncology Rockville, MD Veterinary Technician I, Veterinary Services BS in biology, pharmacology, or related Exp: 1+ years |
Support in vivo oncology studies in mice as a member of the Veterinary Services Team. Conduct daily and weekly assessments and treatments of animals identified with abnormalities. Administer the health surveillance program as described, including animal and sample submission and tracking of results. Proficiently perform survival animal surgeries and provide perioperative care. Collect blood and tissue samples as dictated by study protocol or veterinary need | 5/17/2019 |
| 15319 | Champions Oncology Rockville, MD Research Technician I, Necropsy BS in biology, pharmacology, or related Exp: 1+ years |
Support in vivo oncology studies in mice as a member of Necropsy Services. Allocate animals to study. Assist with gross necropsies (dissection, tissue trimming/collection/preservation, sample collection). Perform preparation activities, including container and tube labeling and room set-up. Collect, process and maintain blood and tissue samples. Assist with the tracking and shipment of samples to sponsors and diagnostic laboratories. | 5/17/2019 |
| 15320 | Champions Oncology Rockville, MD Research Associate, Preclinical Flow Cytometry BS in biological sciences Exp: 1-3 years in cell biology |
The position will work in the flow cytometry laboratory handling samples and preparing for flow cytometry evaluation. Perform standard cell biology techniques to process blood and tissue samples from multiple species. The laboratory process samples in a high-throughput, plate-based manner, requiring ability to use multichannel pipetting. Solid tissue and tumor samples will be dispersed into single cell suspensions. Samples may require cell counting and viability determination using cellometer, hemocytometer, flow cytometer, or other techniques. Sample handling may include cell washing, red blood cell depletion, stimulation, intracellular staining, fixation. Staining of samples with multicolor antibody cocktails. Some PBMC isolation and freezing down cells to create cell banks. Some tissue culture work may be required. He/she will follow SOPs and methods, and carefully record and document processes performed within the laboratory. | 5/17/2019 |
| 15321 | Champions Oncology Rockville, MD Formulation Technician I BS in chemistry, pharmacology, or related Exp: 1+ years |
Provide chemistry and formulation support for vivo oncology studies. Collect and document pertinent data, including lot information, COA, and MSDS, for the receipt, distribution, preparation and disposition of test compounds, reagents, and carriers/vehicles in compliance with appropriate SOPs, GLPs, and regulatory agency guidelines. Prepare and dispose of test materials, vehicles, and reagents according to study protocols and SOPs. Monitor test materials and help maintain facilities for cleanliness, safety, and regulatory compliance. This includes glassware and waste processing. | 5/17/2019 |
| 15322 | Champions Oncology Rockville, MD Cell Culture Assistant BS in biology, pharmacology, or related Exp: 1+ years |
Support in vivo oncology studies in mice as a member of Cell Culture Team. Prepares passaged and primary cells for use by in vivo and in vitro technicians as directed. Produces, maintains and characterizes cultured cells, as directed. Performs related general duties such as inventorying supplies and reagents, general lab housekeeping, and maintaining safety records. Maintain accurate and detailed records using laboratory information management systems and Microsoft Office suite programs | 5/17/2019 |
| 15323 | C4 Therapeutics Watertown, MA Research Associate - Target Biology BS in biology or related Exp: 1-5 years lab experience |
The candidate will play a significant role in the implementation of in vitro studies to characterize and differentiate the biological consequences of our small molecule therapeutics to advance early drug discovery programs. Responsibilities include: Perform cell-based studies to support identification/validation/differentiation of small molecule mechanism of action. Routine implementation of a wide variety of laboratory techniques: mammalian cell culture, cell-based genetic engineering (lentiviral, CRISPR), flow cytometry, etc. Maintain written records of laboratory experiments, data, conclusions and communicate results in a clear/concise manner. | 5/15/2019 |
| 15324 | CSL Holly Springs, NC Specialist I QA (Quality Engineering) BS in science or engineering Exp: 0-3 years |
The incumbent will be a member of the QA-Engineering team at the Holly Springs Influenza Vaccine manufacturing facility, supporting QC/Bulk and/or Fill-Finish Operations. The QA-Engineering Specialist applies Seqirus quality principles related to equipment qualification, method validation, process validation, Cleaning validation, shipping validation and technology transfers. Utilizes integrated commissioning and qualification principles to ensure compliance of equipment and system qualification. Supports the development and maintenance of quality procedures and systems related to Quality Assurance oversight. Provides technical support for the US FCC site in all cGMP compliance related matters, including assurance that all aspects comply with cGMPs, legal, and regulatory requirements. | 5/15/2019 |
| 15325 | CSL King of Prussia, PA Business Systems Analyst I - Identity and Access Management BS in information technology/management or computer sciences Exp: 0-2 years in IT |
Key responsibilities include: Participates in gathering requirements (user requirements, business process requirements) from business users using appropriate mechanisms and following CSL standards. Responsible for identifying the design of approved changes and updating/creating the required system design documentation (design details, diagrams and charts, functional and configuration specifications) to ensure the visualization of the technical implementation. Contributes to the compilation of validation testing. Responsible for the ongoing operation and maintenance of applications for the assigned IT functional areas. This includes providing 2nd or 3rd level incident support, change management, and maintaining the upkeep of technical records and documentation. | 5/15/2019 |
| 15326 | CSL Holly Springs, NC Associate I, Manufacturing (Support) Day Shift HS Diploma/GED or BS/BA Exp: HS: 1+ years, BS: 0 years |
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (or be trained in) the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant, efficient, and cost effective manner. Responsibilities include: Ability to learn basic processes and equipment and serves as a hands-on resource in Production. Cleaning, preparing, and sterilizing production equipment. Assembly, set-up, and disassembly of production equipment. Interfacing with process automation systems and electronic business systems (e.g, PAS, BAS, PLCs, LIMS, SAP, LiveLink) | 5/15/2019 |
| 15327 | CSL Holly Springs, NC Associate I, Manufacturing (Upstream) Night Shift HS Diploma/GED or BS/BA Exp: HS: 1+ years, BS: 0 years |
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (or be trained in) the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant, efficient, and cost effective manner. Responsibilities include: Ability to learn basic processes and equipment and serves as a hands-on resource in Production. Cleaning, preparing, and sterilizing production equipment. Assembly, set-up, and disassembly of production equipment. Interfacing with process automation systems and electronic business systems (e.g, PAS, BAS, PLCs, LIMS, SAP, LiveLink) | 5/15/2019 |
| 15328 | Cambrex Charles City, IA Quality Engineer BS in chemical engineering or chemistr Exp: 1-3 years in manufacturing |
The Quality Engineer will be responsible for oversight and management of open items in the TrackWise system and help facilitate closure of items to achieve site quality goals. This role will help manage all open items to ensure items assigned to others are being completed in the required timeframe and/or assist with updating scope or completion timeframe. This role will also provide hands on work such as completing training, revising documents, completing investigations/CAPA, and executing action plans as it pertains to Project Records (PR) within the TrackWise system. | 5/15/2019 |
| 15329 | Cambrex Whippany, NJ Microbiologist I BS/BA in biology or microbiology Exp: 1-2 years |
The Microbiologist will maintain product quality by conducting microbiology associated tests and monitoring on the manufacturing and packaging environments and systems while adhering to cGMP guidelines. Responsibilities include: Perform Environmental Monitoring by sampling: Total Particulates, Viable Air, Surfaces. Support aseptic processing in a clean room environment including the ability to aseptically gown in to an area and monitor the environment. Sample the water systems and perform the microbiology testing on water samples: Bioburden and Bacterial Endotoxin testing. | 5/15/2019 |
| 15330 | Cambrex Longmont , CO QC Scientist BS/BA Exp: 1-2 years in chromatography or wet analytical chemistry |
As an Analytical Scientist in our Quality Control unit, you will perform release and stability testing of materials for manufacturing of drug substances and drug products including raw materials, starting materials, intermediates, excipients and cleaning samples. You will operate HPLC, Dissolution, GC, KF, FTIR, and other laboratory equipment in a cGMP environment. Additionally, you may write standard operating procedures (SOPs), stability protocols and reports. | 5/15/2019 |
| 15331 | Cambrex Longmont , CO Formulation Scientist BS/BA Exp: 1-2 years in industry |
The Scientist will be responsible for developing oral solid dosage formulations for drug product process development and analytical method development to primarily support early stages of the CDMO projects. In addition to extensively interacting with cross functional teams, individuals are responsible for carrying out and overseeing formulation development and stability testing of lyophilized and liquid formulations. Uses fit for purpose analytical methods to support formulation development, and research stability testing. Authors and reviews formulation development sections of regulatory and technical documents, study reports and technology transfer documents. | 5/15/2019 |
| 15332 | Cambrex Agawam, MA Quality Assurance Specialist II MS degree Exp: 1+ years |
QA Specialist II will be required to: Support the quality team to achieve quality goals. Assist the quality team daily to accomplish efficient and effective review and approval of records as assigned including, but not limited to: calibration and maintenance work, procedures, validation protocols, validation reports, deviations and change controls. Communicate effectively with internal personnel, as well as external customers (if applicable). | 5/15/2019 |
| 15333 | Cardiovascular Systems, Inc Houston, TX Assembly Technician HS Diploma/GED Exp: 1+ years |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. | 5/15/2019 |
| 15334 | Caris Life Sciences Denver, CO JIT Network Associate BS/BA preferred Exp: 1-3 years at clinical sites |
This role has the responsibility to assist in developing and maintaining site research relationships, ensure sites are appropriately trained on JIT research technologies and clinical trial portfolios, and ultimately create an outstanding site research experience. The individual will work closely with the Senior Director, JIT Trials and JIT Network Manager to develop and execute network management and development programs. Arrange and organize sales oriented presentations or trainings for new research sites interested in joining the JIT Network and/or current sites in the JIT Network. | 5/15/2019 |
| 15335 | Caris Life Sciences Phoenix, AZ Laboratory Operations Specialist HS Diploma/GED Exp: 1-3 years in lab |
The Laboratory Operations Specialist is responsible for supporting all CMI laboratory departments with all clerical and ancillary duties in keeping all equipment ready to run for patient output. While maintaining job functions, the Laboratory Operations Specialist is to progress in their learning of the regulations (CLIA, CAP and NYS) which the laboratory functions by. Laboratory Operations Specialists support Specimen Processing Clerks, Histology Technicians, Histology Technologists, Pathology Assistants, Pathologists and Molecular Technicians. This position works under the direction of the Supervisor and follows standard laboratory procedures and policies. | 5/15/2019 |
| 15336 | Zeiss Orlando, FL Field Support Engineer I BS in electronics, engineering, or computer technology Exp: 0-3 years in field service |
The Field Support Engineer I, under close supervision and direction, installs, repairs, upgrades and performs preventative maintenance on specified Carl Zeiss Meditec instrumentation in a designated field service territory. Represents Carl Zeiss Meditec at customer locations and works to achieve a high level of customer satisfaction. Maintains all company property (inventory, tools, diagnostic equipment, vehicle, etc.) in accordance with company policies. Maintains a high level of professional communication with team, customers, management, Sales and Technical Support. | 5/15/2019 |
| 15337 | Zeiss Kansas City, MO Field Support Engineer I BS in electronics, engineering, or computer technology Exp: 0-3 years in field service |
The Field Support Engineer I, under close supervision and direction, installs, repairs, upgrades and performs preventative maintenance on specified Carl Zeiss Meditec instrumentation in a designated field service territory. Represents Carl Zeiss Meditec at customer locations and works to achieve a high level of customer satisfaction. Maintains all company property (inventory, tools, diagnostic equipment, vehicle, etc.) in accordance with company policies. Maintains a high level of professional communication with team, customers, management, Sales and Technical Support. | 5/15/2019 |
| 15338 | Zeiss Boston, MA Field Applications Scientist MS in biological sciences or bio-engineering Exp: 0-3 years |
The job involves training and working with scientists and microscopy users across the territory on a regular basis. The Field Applications Scientist will represent ZEISS as an expert in topics including, but not limited to Widefield, Confocal, Airyscan, Superresolution, Lightsheet and Automated microscopy, Image Processing and Image Analysis. Exceptional documentation and organizational skills are essential to succeed in this position. In addition to effectively communicating complex microscopy concepts to our customers, effective coordination between members of the sales and service team is an integral part of the daily routine. | 5/15/2019 |
| 15339 | Zeiss Marlborough, MA Applications Engineer - Metrology Services BS/BA in engineering, math or physics Exp: 0-5 years |
Job Duties include: Consistent delivery of acceptable customer results. Ability to setup and run all lab measurement equipment. Ability to select and use the best software for the job (Calypso, VG StudioMax, etc.). Deliver inspection reports per the job request. Monitor each system’s performance for accuracy/repeatability issues. Peer review job results with colleagues. Assist Site Manager with quoting as necessary. Results review with customer (within 2 days of job completion – if possible). | 5/15/2019 |
| 15340 | Casebia Therapeutics Cambridge, MA Process Development Engineering Associate MS in biologica/chemical sciences Exp: 1+ years |
The position will be responsible for downstream purification of recombinant viruses and will be a key member of the team developing expression and purification strategies for novel gene editing/gene therapy vectors. Responsibilities include: Contribute to a smart, integrated development approach for definition of scalable viral vector processes and suitable control strategies. Plan and perform experiments to develop purification process steps including chromatography (affinity, IEX, HIC, SEC, etc.) and filtration (depth filtration, UFDF, and sterile filtration). Perform experiments to develop robust downstream unit operations, using DoE, multivariate analysis, and other statistical tools. | 5/15/2019 |
| 15341 | Casebia Therapeutics San Francisco, CA Research Associate, in vivo BS or MS in biology or realted Exp: 0-2 years |
The successful candidates will be integral in discovering and developing the next generation of therapies for hematological diseases. The successful candidates will have experience executing and analyzing in vivo experiments in hematology, specifically the hematopoietic and immune system. Basic cell and molecular biology skills are desirable. | 5/15/2019 |
| 15342 | Casma Therapeutics Cambridge, MA Research Associate - Cell Lines, Biology MS in biology or related Exp: 1-3 years |
The individual should possess strong core competencies in cell biology, molecular biology, assay development. Responsibilities include; Cell culture and cell line development using retro- and lenti-virus, CRISPR and downstream analysis of autophagy and signaling. Perform western blotting, FACS and imaging analysis to analyze autophagy and specific target activity in primary cells and cell lines. Aid in conducting genome-wide CRISPR screens for novel target ID. Use mouse tissue to both aid in the development of novel biomarkers and analyze key targets by protein and gene expression. | 5/15/2019 |
| 15343 | Catalent Madison, WI Biomanufacturing Upstream, Associate Two BS/BA in biotechnology or reated Exp: 0-2 years |
As a Biomanufacturing Upstream, Associate Two you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) Biomanufacturing activities. Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Perform basic cell culture work, including but not limited to working inside of a biosafety cabinet, cell counting (automated and manual), performing manipulations of required cell cultures in an ISO 5 environment, and analysis of cell culture samples using applicable analyzers. | 5/15/2019 |
| 15344 | Catalent Madison, WI Associate, Biomanufacturing BS/BA in biotechnology or reated Exp: 0-2 years |
As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position. Work hours are Sunday to Wednesday (4/10). Responsibilities include: Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) revisions, deviation investigations and change control/protocol execution, by established due dates. | 5/15/2019 |
| 15345 | Catalent Madison, WI Associate Quality Assurance Systems, Document Control BS/BA in biotechnology, engineering, or life sciences Exp: 0-2 years |
The Associate Quality Assurance Systems, Document Control is responsible for managing the flow of document review, making documents effective and distribution according to standard operating procedure (SOP). The Associate Quality Assurance Systems, Document Control will correspond with customers to obtain document approval. Responsible for the process of document control, including managing drafts, editing, approval, change control, distribution and archiving, of all controlled documents (e.g. Standard Operating Procedures (SOPs), Batch Production Records, Stability Protocols, Qualification Protocols, Specifications, Equipment Records, etc). Edits Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and reports independently and accurately. | 5/15/2019 |
| 15346 | Catalent Madison, WI Laboratory Associate Buffer Prep, Manufacturing AS/AA in biotechnology or reated Exp: 0-1 years |
Catalent has an opening for a Laboratory Associate Buffer Preparation, Manufacturing position. Responsibilities will include performing aseptic techniques within a clean room environment. As the Laboratory Associate Buffer Preparation, Manufacturing you will learn to execute and properly document biomanufacturing activities. Work schedule is Wednesday to Saturday, 7:00 a.m. to 5:00 p.m. CST. Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). | 5/15/2019 |
| 15347 | Catalent Morrisville, NC Laboratory Associate BS/BA in chemistry or realted Exp: 0 years |
Performs tasks from detailed instructions and established procedures. After conducting basic analysis, interpretation and evaluation of results, work is reviewed for soundness of judgement and adherence to procedure. Execute laboratory work plan / schedule developed by supervisor or senior team member. Edits technical documents, such as test methods, with direct guidance from a supervisor or senior level scientist. | 5/15/2019 |
| 15348 | Catalent Woodstock, IL Formulation Technician HS Diploma/GED Exp: 1+ years in manufacturing |
The Formulation Tech reports to the Production Manager. The position is entry level and responsible for learning the basic BFS technology, personal protective equipment, equipment use, and comprehension of formulation processes and methods such as: tank sterilization process, temperature recorder function, reading set-up drawings, tank compounding, and batch record documentation. This position is responsible for aseptic gowning certification as prerequisite to entering the Aseptic Suites. New hire is not intended to stay in this position long term. Once training and qualification is completed at this level, employee advances to Formulation Technician Level 1. | 5/15/2019 |
| 15349 | Cato Research Durham, NC Biostatistician I BS or MS in sciences Exp: 1-2 years |
Responsibilities include: Write and review statistical analysis plan. Write and review the statistical and related sections of clinical protocols. Provide statistical guidance and input to authors of clinical study reports, development plans, and other regulatory documents to ensure accuracy and quality. Interacts with sponsors, investigators, and other consultants to determine the best clinical trial design. Performs the design, development, modification, and evaluation of technical infrastructure to expedite conduct and evaluation of clinical trials and basic research | 5/15/2019 |
| 15350 | Celerion Montreal, QC Clinical Data Programmer I BS in statistics, math, computer sciences or related Exp: 1+ years |
Responsibilities as a clinical data programer include: Provide data programming support to project teams for reporting and analysis of clinical data in early clinical studies. Develop, maintain and process SAS programs for standard studies that create case report forms (CRFs), edit checks (clinical), data listings, analysis data sets and electronic data transfers. | 5/15/2019 |
| 15351 | Celerion Lincoln, NE Clinical Data Programmer I BS in statistics, math, computer sciences or related Exp: 1+ years |
Responsibilities as a clinical data programer include: Provide data programming support to project teams for reporting and analysis of clinical data in early clinical studies. Develop, maintain and process SAS programs for standard studies that create case report forms (CRFs), edit checks (clinical), data listings, analysis data sets and electronic data transfers. | 5/15/2019 |
| 15352 | Celerion Lincoln, NE Associate Quality Control Analyst AS/AA or BS/BA in chemistry, biology, or related Exp: 0-1 years |
Responsibilities include: Verify Excel spreadsheets and calculations. Assist in paperwork routing, document assembly, and verification of information packet completeness. Verify raw data against information in Methods or Standard Operating Procedures: Ensure Compliance with general SOP requirements, Verify Solution composition or concentration, including calculations used to determine the concentrations are correct, Verify volumes used and any processing step documented are as explained in the sample processing procedures | 5/15/2019 |
| 15353 | Celgene Summit, NJ Manufacturing Associate, CAR-T BS/BA Exp: 0-2 years |
Manufactures human blood derived components per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. This position is for the Weekday Shift Start and end times are subject to change based on business demands. | 5/15/2019 |
| 15354 | Cell Signaling Technology Danvers, MA Research Associate - Monoclonal Development BS/BA in biological sciences Exp: 1+ years lab experience |
The Research Associate is a member of the Monoclonal Development team which is a core function for antibody development at CST. This individual will be responsible for preparing rabbit and mouse monoclonal antibodies as one of the key first steps in our product development process. This will be a focused role that will provide exposure to the broader monoclonal antibody development process. Coat and block plates for ELISA preparation, Process and document resulting ELISA data in accordance with CST hard copy and electronic laboratory documentation requirements (e.g. notebooks, electronic LIMS, Jira, PDP, PLM, etc.) Make culture media | 5/15/2019 |
| 15355 | Cell Signaling Technology Danvers, MA Lab Assistant II HS Diploma/GED, BS/BA preferred Exp: 1+ years |
We are seeking a Lab Assistant who will work as part of the Development Materials Management Core (DMMC), which serves as a centralized resource for the Product Development organization. The DMMC manages the inventory of antibody materials integral to antibody validation pipeline and enables reduced product development cycle times through the efficient, effective, and timely delivery of materials between the Antibody Discovery teams, other groups in Product Development, and Production teams. Responsibilities include: Accurately track and properly store antibody samples and other materials used to validate antibodies. Receive and log new materials, both made in-house (e.g. those produced by the Validation Systems Core (VSC)) and ordered commercially, into inventory management system on a timely basis. etc | 5/15/2019 |
| 15356 | Cell Signaling Technology Danvers, MA Research Associate BS/BA in biological sciences Exp: 1+ years lab experience |
We are seeking a Research Associate to join our Validation Systems Core (VSC) team within our Product Development organization. The VSC serves as a centralized resource for innovation in the culture, treatment, lysis, and storage of cell lines. The Research Associate is responsible for providing well-characterized, high quality cells and lysates to the organization to support Product Development efforts focused primarily on affinity research reagents such as primary antibodies, in addition to other product types such as assay kits, conjugates, and ELISA pairs. | 5/15/2019 |
| 15357 | Boston Scientific Tampa, FL Rhythmia Mapping Specialist BS in biomedical engineering or related Exp: 0-2 years |
The Rhythmia Specialist will provide expert clinical product and technical assistance and training to physicians, EP Lab Staff, and sales representatives on the effective and safe use of the Rhythmia System during case procedures within an assigned geography, and in a manner that leads to meeting and exceeding business goals. Serves as primary resource for clinical support in the areas of case coverage, basic troubleshooting, system/software development for Rhythmia System and catheters. Educates customers and internal BSC employees on the merits and proper clinical usage of Rhythmia by giving presentations and demonstrations using a wide variety of formats and platforms (e.g., slides, transparencies, manuals) to keep all abreast of the latest product and technology developments for Rhythmia system. | 5/13/2019 |
| 15358 | Boston Scientific Coventry, RI Process Engineer I BS/BA in mechanical or chemical engineering Exp: 0-2 years |
The Process Engineer I is responsible for developing and maintaining capable processes and ensuring efficient and effective sterilization operation. This person will apply problem solving skills to enable sterilization innovation while using technical and collaboration skills alongside his/her passion for innovation and continuous improvement to drive growth through efficient and effective process improvements. Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on multiple and moderately complex processes. Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation. | 5/13/2019 |
| 15359 | Boston Scientific Valencia , CA Research Scientist II MS in biomedical engineering, neuroscience, or related Exp: 1+ years in neural engineering |
The Research Scientist II will support execution of neuromodulation research projects (computational, preclinical, and exploratory clinical studies). The successful candidate will primarily focus in the area of deep brain stimulation, supporting future technologies and participating in the definition and execution of multiple projects that address strategic, scientific, and technological needs for the organization. | 5/13/2019 |
| 15360 | Brammer Bio Alachua, FL Scientist - Downstream PD BS/BA or higher Exp: 1+ years |
The Scientist will provide biologics process development support to ensure that the Brammer Bio Downstream Process Development (DSPD) unit operates to provide clients with new purification methods and investigational materials for pre-clinical and clinical use. The incumbent will assist in the design and execution of experiments under the supervision of the technical project lead. This will involve researching and sourcing reagents, equipment, and materials; preparing columns; purifying viral vectors utilizing working knowledge in filtration technologies, column chromatography (SEC, affinity, HIC, AEX), ultracentrifugation and scale up principles. This position will also be expected to technically review data, prepare experiments/data for presentation, participate in laboratory investigations, interpret this data and work with the project lead to trouble-shoot technical problems. The incumbent will participate in the optimization of purification methods and the writing and troubleshooting of protocols. The incumbent is expected to prepare and modify documents (SOPs, Batch Records, Raw Material Specifications, etc), maintain a GLP culture, and assist in maintaining the process development laboratory. | 5/13/2019 |
| 15361 | Brammer Bio Cambridge, MA Manufacturing Investigator I BS/BA Exp: 1-5 years |
The Manufacturing Investigator I in this role will be part of a cohesive team responsible for Deviations and CAPAs for all phases of manufacturing. The Manufacturing Investigator I uses expert knowledge of cGMP regulations and project management to ensure manufacturing readiness. The incumbent will also support investigations and improvement initiatives within the manufacturing operations. Works independently with minimal supervision and direction. Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion. | 5/13/2019 |
| 15362 | Brammer Bio Cambridge, MA Associate, Manufacturing Science & Technology BS in biochemical or chemical engineering, or realted Exp: 0-2 years |
The primary responsibility is to support the technology transfer teams for the late stage, PPQ and commercial manufacturing of viral vectors. This position requires close interaction with the MS&T colleagues, Manufacturing, Process Development, and other departments. This role will focus on aspects of ensuring a robust, scalable and efficient manufacturing processes to produce late-phase human clinical trial and commercial gene transfer vector products. Supports cross functional technology transfer teams for cGMP DS manufacturing of viral vectors. Collaborate with another site or clients to ensure success of scale up/ process transfer. Includes authoring of upstream or downstream plan documentation and associated detail process descriptions (DPDs). | 5/13/2019 |
| 15363 | Brammer Bio Cambridge, MA Associate I, Quality Control (Microbiology) BS/BA in biology, chemistry, or related Exp: 0-2 years |
(Overnight Position) The QC Associate I will work in the QC cGMP compliant Laboratories to develop, qualify, and conduct microbiological assays that support quality control of biopharmaceutical products being developed and manufactured at Brammer Bio under contract. Normal working hours will be 7:00 pm - 7:00 am on a shift rotation. Occasional off-shift work/holiday work will be required to support business needs. Duties include performing routine microbiological assays and testing including but not limited to environmental monitoring, bioburden and endotoxin testing. The QC Associate I will also troubleshoot and optimize assays under the supervision of QC Microbiology management . Functions also involve raw data review and document management, maintenance (routine and preventive operation) of equipment, and supporting routine laboratory operations (cleaning the laboroatory, inventory control, etc) | 5/13/2019 |
| 15364 | Bristol-Myers Squibb Devens, MA Associate Scientist/Engineer MS in pharma, biological, or chemical sciences/engineering Exp: 0-2 years |
Responsibilities include: Conduct experiments to support cryogenics manufacturing processes of commercial and late-stage biologics drug substance. The candidate will support bulk container selection and freezing, storage, and thawing operations for biologics drug substance. Support validation of the freezing and thawing processes of commercial and late-stage biologics drug substance across BMS global network and contract storage/manufacturing sites. Follow appropriate GLP/GMP procedures. Study design, execution and analysis of results, data verification, preparation of study protocols and final reports, and the presentation of findings at internal and external forums | 5/13/2019 |
| 15365 | Bristol-Myers Squibb New Brunswick, NJ Process Engineer BS or MS in chemical engineering/chemistry/engineering Exp: 1-3 years |
As API Process Engineer, you will work as part of a cross-functional matrix team to ensure successful manufacture of active pharmaceutical ingredients, chemical intermediates and specialty materials to support development of R&D pipeline products. Provide process engineering expertise within process planning workflows and document reviews for internal and external manufacturing implementation including: tech transfer documentation, data/process knowledge collection, equipment setup, process modeling, process flow diagrams, compatibility assessments, risk management, etc. Perform engineering analysis of process execution, recommends opportunities for improvement with plant efficiency and risk mitigation as goals, and captures analysis in campaign summary documents | 5/13/2019 |
| 15366 | Bristol-Myers Squibb Hopewell, NJ Associate Research Scientist MS in analytical chemistry, biochemistry, or related Exp: 0-2 years |
This associated scientist position within the analytical methods team has the opportunity to drive the development and validation of robust separation methods (e.g., CE-SDS, iCIEF, SEC, RP, IEX, HIC) for biotherapeutic drug candidates in the portfolio spanning early and late stage clinical programs. Bristol-Myers Squibb's biologics pipeline includes approved biologics products such as OPDIVO®, YERVOY®, EMPLICITI®, ORENCIA®, and NULOJIX®, and a number of exciting clinical stage compounds as well as antibody combination products. Development of methods utilizes state-of-the-art analytics as well as modern concepts of quality attribute monitoring of biotechnology products. Science-based research and molecular-level understanding of protein properties are critical for successfully performing method development. Innovation is central to establishing robust analytical control and define our overall biologics development strategy. The successful candidate will also support regulatory filing activities including IND and BLA, as necessary. This position reports to manager in Methods and Analytical Development function of the Biologics Development organization. | 5/13/2019 |
| 15367 | Bristol-Myers Squibb Devens, MA Engineer/Scientist Rotational Program BS in chemical engineering/life sciences Exp: 0-2 years |
Support the operation of GMP / Non GMP manufacturing systems (Systems include Process Automation Systems, Manufacturing Execution Systems, Process Development, Technology Transfer, Laboratory, Manufacturing Operations) in the associated facilities. Provide Troubleshooting support and guidance of systems in support of manufacturing, process development, and/or Lab operations within a collaborative team. Collaborate in investigations of proprietary automation software/hardware, manufacturing operations, process development, along with vendors when necessary. Documentation of data and results, data verification, interpretation of small scale and at scale data supporting the manufacturing processes and preparation of final reports to summarize the findings. | 5/13/2019 |
| 15368 | Bristol-Myers Squibb Devens, MA Assistant Engineer/Scientist Rotational Program BS in chemical engineering/life sciences Exp: 0-2 years |
Support the operation of GMP / Non GMP manufacturing systems (Systems include Process Automation Systems, Manufacturing Execution Systems, Process Development, Technology Transfer, Laboratory, Manufacturing Operations) in the associated facilities. Provide Troubleshooting support and guidance of systems in support of manufacturing, process development, and/or Lab operations within a collaborative team. Collaborate in investigations of proprietary automation software/hardware, manufacturing operations, process development, along with vendors when necessary. Documentation of data and results, data verification, interpretation of small scale and at scale data supporting the manufacturing processes and preparation of final reports to summarize the findings. | 5/13/2019 |
| 15369 | Brooks Chelmsford, MA Mechanical Engineer MS Exp: 0-1 years |
Responsible for design/development, modification, and evaluation of primarily mechanical systems, equipment and packages. May contribute to total systems engineering, including other eng. disciplines. Conducts feasibility studies and tests new and modified designs. Is involved in all phases of development from initial concept to manufacturing. Directs support personnel in the preparation of detailed design, design testing and prototype fabrication. Provides design information to drafting for packaging documentation. Depending on level may function as a project engineer/leader with the resident responsibilities of proposals/project plan, schedules, work assignments, prime contact, technical presentations, cross functional issue resolution, etc. | 5/13/2019 |
| 15370 | Bruker Kennewick, WA Manufacturing Engineer & Quality BS in mechanical, electrical or industrial engineering Exp: 1-5 years |
As a Manufacturing Quality Engineer, you will be the primary quality interface for new and existing products. You will design, develop, and execute quality assurance and control systems. Use your expertise and judgment in implementing a wide variety of quality concepts, practices, and procedures. You will contribute to product and manufacturing process design, as well as the methods for verification and validation of product to ensure adherence to company and customer requirements. You will work toward the prevention and/or resolution of product and manufacturing process non-conformance. You are well versed in working with Contract Manufacturers (CM) and Component Suppliers. You will lead teams to ensure products are designed and built to Bruker’s high standards of quality and performance. You will evaluate the product designs and create the processes, tools and procedures behind Bruker’s world leading Handheld X-Ray Fluorescence (XRF) products. You will collaborate with Commodity Managers and Design Engineers to determine Bruker’s manufacturing and product specifications | 5/13/2019 |
| 15371 | BD Tempe, AZ R&D Engineer II MS in engineering Exp: 0-3 years |
This position designs, develops and implements new products, processes, test methods and equipment. This position is responsible for conducting engineering studies for process improvements and validations. Initiates new or revised documentation and tracks through appropriate approval cycles and implementation. Maintains a professional working relationship with internal and external customers and support staff. Develops physical and functional test requirements to ensure specifications and regulations are met. Writes and approves protocols, reports and data. | 5/13/2019 |
| 15372 | BD Woburn, MA Associate Manufacturing Engineer BS in chemical engineering Exp: 0-1 years |
Responsible for coordinating and providing engineering support throughout the manufacturing facility in areas such as process improvements, technological advancements, cost improvements, facility maintenance, safety, and environmental regulation. Coordinate and participate in plant CIP and process improvement programs as required.Support, or lead as required, activities such as failure investigation, design of experiments, process capability studies, qualifications, and validations of processes and equipment. Coordinate tactical plans geared towards timely completion of line extensions and major equipment installations, modifications, or enhancements. | 5/13/2019 |
| 15373 | BD Covington, GA Quality Engineer I BS in engineering/sciences Exp: 1-3 years in regulated industry |
This position is responsible for working in the Bard Complaint Laboratory to perform product testing as well as planning, organizing, and tracking work activities. Quality results are expected to ensure the integrity of Bard complaint investigations. Additionally, the Quality Engineer functions as a subject-matter resource for Engineering, Operations, Sterilization and outside suppliers. Responsible for all products testing in the Complaint Laboratory. Creates investigation files in the BARD Global complaint system (Trackwise). | 5/13/2019 |
| 15374 | Bio-Techne Minneapolis, MN Research Associate, Cell Culture and Stem Cell Media Operations BS/BA in biological sciences Exp: 0-2 years lab experience |
The responsibilities of this position are production, bottling, and packaging of methylcellulose-containing and other cell culture media. Perform QC testing of methylcellulose-containing cell culture media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Skills used include cell culture, high attention to detail, strong communication and organizational skills. Perform additional duties as assigned. This will be a Sun through Thurs work schedule. | 5/11/2019 |
| 15375 | Bio-Techne Minneapolis, MN Research Associate, Cell Culture and Stem Cell Media Operations BS/BA in biological sciences Exp: 0-2 years lab experience |
The responsibilities of this position are production, bottling, and packaging of methylcellulose-containing and other cell culture media. Perform QC testing of methylcellulose-containing cell culture media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Skills used include cell culture, high attention to detail, strong communication and organizational skills. Perform additional duties as assigned. This will be a Sun through Thurs work schedule. | 5/11/2019 |
| 15376 | Bio-Techne Minneapolis, MN Research Associate, Q Kit Assay Development BS or MS in biological sciences or related Exp: 0-2 years lab experience |
The responsibilities of this position are to primarily develop immunoassay kits including reagent evaluation, feasibility, assay optimization, stability studies and product transfer. Develop new immunoassay products. Under general supervision, independently schedule, plan, perform and report experiments for the feasibility, optimization, transfer and validation of immunoassay kits. Communicate effectively in writing and in verbal communications, including formal presentations. Write official product documentation. | 5/11/2019 |
| 15377 | Bio-Techne Minneapolis, MN Research Associate/Advanced Research Associate Antibody Development BS/BA of biochemistry, cell biology, chemistry Exp: 0-5 years |
The responsibilities of this position are to characterize monoclonal and polyclonal antibodies on natural samples using Western blot and Simple Western. Screen multiple sera or hybridoma culture supernates to select potential products. Validate purified antibodies using natural samples. The person will develop problem solving and decision-making skills, while maintaining appropriate contact and communication with the supervisor. Maintain and treat cell lines for needed lysates. Refer to pertinent literature, databases and competitor product information on specific antibody targets. Maintain clear notebook, enter data in PDPT and perform calculations. | 5/11/2019 |
| 15378 | Bio-Techne Minneapolis, MN Kit Packer I HS Diploma Exp: 0-2 years |
The responsibilities of this position are to package and release all kits manufactured by bio-techne (including set-up, component inspection, label printing) as defined in the packaging procedures. Inspect and release proteins and antibodies to Finished Goods Receiving. Cap and label proteins and antibodies as necessary. Break down expired kits and properly dispose of all components. Participate in annual cycle counts and/or as needed. | 5/11/2019 |
| 15379 | Bio-Techne San Marcos, CA Manufacturing Chemist I BS in chemistry/biochemistry, or biological sciences Exp: 0-2 years |
The Manufacturing Chemist I is responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 5/11/2019 |
| 15380 | Bio-Techne Minneapolis, MN Research Associate - New Technologies/Luminex MS in chemistry, biology, or related Exp: 0-2 years |
The responsibilities of this position are to assist with validation, feasibility, product development, and technical support of immunoassays. Optimize components and performance, develop manufacturing procedures, transfer product/process to production, and perform necessary troubleshooting. Work on problems of moderate scope where analysis of situation or data requires a review of identifiable factors. Perform additional duties as assigned. | 5/11/2019 |
| 15381 | Bio-Technical Resources Manitowoc, WI Assistant Research Scientist, Microbiology/Molecular Biology BS/BA or MS in biological sciences/microbiology Exp: 1-3 years |
Bio-Technical Resources is seeking an Assistant Research Scientist to work with supervision as a microbiologist and molecular biologistas part of a team developing new strains for the production of antibiotics, enzymes, metabolites, and proteins. The position involves generating and improving strains using strain engineering molecular biology techniques or classical mutagenesis,screening and selection.Routine microbiology tasks | 5/11/2019 |
| 15382 | Bio-Technical Resources Manitowoc, WI Assistant Research Scientist, Analytical Support BS/BA or MS in chemistry, biochem, or chemical engineering Exp: 1-3 years |
Bio-Technical Resources is seeking an Assistant Research Scientist to work with supervision as an analytical research assistant supporting teamsdeveloping fermentation and biotransformation processes for the production of antibiotics, enzymes, proteins, chemicals, and metabolites. The position involvesimplementation of HPLC, chromatography, enzyme assays, and gel-basedanalytical methods.Common tasks include analytical separations and quantitative analyses | 5/11/2019 |
| 15383 | Biotronik Lake Oswego, OR Clinical Trials Assistant AS or BS/BA in health or sciences Exp: 1+ years |
This position will provide support for clinical research functions of project teams by supporting all aspects of project initiation through project closure. This will include performing administrative functions, maintaining general and study site files, data entry and interfacing with site coordinators, field clinical staff and other company representatives, as well as other project-specific duties. | 5/11/2019 |
| 15384 | bluebird bio Cambridge, MA Associate Scientist, Molecular Biology BS or MS in biological sciences or related Exp: 1-3 years |
This new Research Associate will join our group to develop and evaluate novel gene therapies for oncology and severe genetic disease. Responsibilities include: Independently perform routine protocols for qPCR and RNA-seq. RNA sample preparation, including (but not limited to): RNA isolation, library preparation for NGS and qPCR, quantification and QC. Prepare and sequence cDNA libraries using Illumina sequencing instruments (NextSeq). Analyze and communicate findings to cross-functional group members through presentations, face-to-face meetings and email. | 5/11/2019 |
| 15385 | Boehringer Ingelheim Fremont, CA Manufacturing Associate Upstream-Nights AS or BS/BA in biotechnology or biological sciences Exp: 1+ years lab experience |
(Associate Level) Executes routine unit operations in Upstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures. Executes, with oversight of qualified staff, complex unit operations including but not limited to batching and inoculation of bioreactors, operation of bioreactors, process monitoring, and harvest operations. Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies. | 5/11/2019 |
| 15386 | Boston Analytical Salem, NH Analytical Chemist *All-Levels* BS/BA in chemistry or related Exp: 0-5 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. Responsibilitiesi include: Prepares and analyzes products to determine chemical and physical properties. Follows all safety rules and regulations and conducts periodic safety audits. Under close supervision confers with chemists and other client personnel regarding research, procedures performed, related results and prepares reports. Performs routine data generation and problem solving with a minimal rework. | 5/11/2019 |
| 15387 | Boston Analytical Salem, NH Sample Management Technician HS Diploma Exp: 0-2 years |
Non-Lab position. The Sample Management Technician is responsible for ensuring that all samples are entered into the Laboratory Information Management System (LIMS) and made available to the lab staff in a timely manner. This position reports to the manager of Stability and Sample Management. The Technician’s responsibilities include, but are not limited to, the following: Performs any combination of sample management tasks, including labeling, preparing for shipping, transporting to labs, inventorying and disposing. Reviews and verifies sample paperwork against samples to ensure accuracy and communicate discrepancies. Distributes sample information and paperwork. | 5/11/2019 |
| 15388 | Bioclinica The Villages, FL Psychometric Rater BS/BA in mental health-related field Exp: 1+ year in psychometry or related |
The Psychometric Rater I is responsible for administering and interpreting quantitative tests for the measurement of psychological variables related to diseases and disorders, examples of which include, but are not limited to, Alzheimer’s disease, Mild Cognitive Impairment, Multiple Sclerosis, Depression, Anxiety, and Parkinson’s Disease. This position is responsible for managing the psychometric ratings aspect of clinical trial performance at the site level in order to ensure that the data collection is in congruence with the philosophy and mission of the company, as well as with the specific scale administration guidelines. The Psychometric Rater I follows study-specific protocol guidelines and communicates and interacts with Investigators, clinic staff, sponsoring agencies, and others to effectively perform required testing and related research activities. | 5/10/2019 |
| 15389 | Bioclinica The Villages, FL Clinical Research Coordinator BS/BA in health field Exp: 1+ year in clinical research |
The Clinical Research Coordinator I (CRC I) is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials is congruent with the philosophy and mission of the company. The CRC I plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned research projects. The CRC I follows study-specific protocol guidelines and communicates and interacts with Investigators, clinic staff, sponsoring agencies, and others to effectively perform clinical research and to coordinate research activities. All duties carried out by the CRC I are done so in accordance with company policies and SOPs, as well as all applicable local, state, and federal regulations. Professionals in this role actively participate in outstanding customer service and accept responsibility for developing and maintaining mutually respectful relationships. | 5/10/2019 |
| 15390 | Bioclinica Nashville, TN Imaging Analysis Technician BS/BA in sciences or health Exp: 0-1 years |
Responsibilities include: Communicates with Clinical Project Managers, Clinical Operations Associates and/or Specialists regarding image quality, deliverables, and data discrepancies. Communicates with Image Analysis Lead, Clinical Operations Manager, and/or Scientific Director regarding troubleshooting of reading systems, image quality concerns, and deliverables. Maintains study-specific reading tracking tools. Performs quality control of site qualification- scans using phantom or patient, and on-going patient data within study-specific turnaround times to Clinical Project Manager, Clinical Operations Associate, and/or Specialist responsible for the study. Completes validation of relevant central analysis types by meeting pre-defined validation requirements. | 5/10/2019 |
| 15391 | Bioclinica Durham, NC Associate, Validation Services BS/BA in computer science, engineering, etc Exp: 1+ year in software validation |
Ensures software applications are accurate, complete and conform to all user, company and regulatory requirements by: Tracking all software versions, features, bugs and validation efforts for all software created and/or modified by the Development teams. Creating and executing manual test scrips which includes testing software applications for quality and functionality using defined validation protocol and testing techniques. Working with application developers in resolving issues and retesting applications. Partnering with technical and business teams to achieve understanding of current and future functionality. | 5/10/2019 |
| 15392 | Bioclinica Ocala, FL Medical Assistant HS Diploma Exp: 1+ year as medical assistant |
Medical Assistant works in a clinic setting and handles basic clinical task and performs administrative/office duties. Interacts with patients and assist physician to ensure operations run smoothly and efficiently. Responsibilities include: Answer incoming calls, take messages and/or respond to all calls within 24 hours. Schedule patient appointments. Perform clinical task including but not limited to vital signs and height/weight; document medical history in patient charts. Call and/or fax RX request to pharmacy and obtain preauthorization, if necessary once approved by physician | 5/10/2019 |
| 15393 | Bioclinica Orlando, FL Laboratory Assistant HS Diploma Exp: 1+ year clinical/lab experience |
The Laboratory Assistant must demonstrate knowledge of specimen collection and processing and handling requirements as relevant to Bioclinica Research and must have a thorough knowledge of lab procedures and practices. Responsibilities include: Perform blood draws, specimen collection, take vital signs, perform EKG testing and able to record accordingly. Timely specimen preparation for processing and shipping. Effectively and professionally interact with patients, visitors, peers and other healthcare professionals | 5/10/2019 |
| 15394 | Bioclinica Orlando, FL Laboratory Technician BS/BA in chemistry, biochemistry, or biology Exp: 1+ year lab experience |
The Lab Technician is responsible for the overall specimen processing and handling according to specific protocol requirements and Bioclinica Research SOP. Responsibilities include: Specimen handling, Perform lab tests, Prepare and process blood, urine and other samples for in house test, reference lab or central lab according to specific study protocol and/or SOP, Perform blood draws, specimen collection, take vital signs, perform EKG testing and able to record accordingly | 5/10/2019 |
| 15395 | Biodesix Boulder, CO Laboratory Technician BS/BA in chemistry, physical, biological sciences Exp: |
Biodesix is accepting resumes for a Laboratory Technician to process molecular and proteomic Laboratory Developed Tests (LDT’s) from blood based specimens. Laboratory Technicians must have the technical training and experience required to perform regulated clinical laboratory testing, including sample accessioning and processing using standard in-vitro laboratory techniques which include DNA and RNA extraction from whole blood, ddPCR (digital droplet PCR), Mass Spectrometry for proteomic testing and to operate a proprietary LIMS. | 5/10/2019 |
| 15396 | BioDuro San Diego, CA Quality Assurance Associate – Analytical & Manufacturing Support BS/BA in sciences Exp: 6 months + |
This function includes: Analytical Support – Support functions include, but are not limited to: review and approval of in-process testing, release testing of products, stability testing, other data summaries, method validation data, laboratory equipment validation protocols, product certificates of analysis, generation of environmental chamber monitoring reports. Other duties as deemed appropriate by Head of Quality. Manufacturing Support, Document Control, Internal Audits and Client / Regulatory Audits, Equipment and Facilities Calibration, Maintenance, Validation, Preventive Maintenance | 5/10/2019 |
| 15397 | BioLegend San Diego, CA Manufacturing Associate - Tissue Culture AS/AA in biology, biochemistry, or related Exp: 6 months + |
The primary functions of this position include culturing, setting up, feeding, maintaining, and harvesting of bioreactors with hybridoma cells, finding, testing, and developing new procedures to increase the quality and efficiency of our product and processes, and maintenance of regularly used equipment. This position offers a varied work load and will enable you to gain solid experience that will allow you to grow and increase your skill set within a fast-growing and stable biotech company. This position will also allow you to gain experience in all areas of tissue culture and cross training on a variety of other supporting tasks such as downstream processing, ELISA assays, qPCR, mycoplasma detection, and NOVA BioProfile 400 use and maintenance. | 5/10/2019 |
| 15398 | BioLegend San Diego, CA Product Development Research Associate - Recombinant Protein Group BS/BA in biological sciences Exp: 1 year |
The Product Development Research Associate will be responsible for developing cutting edge recombinant protein research products for the Molecular Cellular Immunology group. This position will be involved with developing a new line of recombinant protein products by supporting other team members. The typical duties include preparing buffer solutions and cell culture media, performing bacterial and mammalian cells cultures, purifying recombinant proteins with affinity tag, and performing PCR and DNA purification according to standard operating procedures. | 5/10/2019 |
| 15399 | BioLegend San Diego, CA Manufacturing Associate - Conjugation (1st Shift) AS/AA in biochemistry, chemistry or related Exp: 1+ year |
The Manufacturing Associate will be an integral member of a team that ensures the highest quality of our finalized antibody products. This position offers the opportunity to gain experience with different types of conjugation chemistries and different chromatography methods to purify antibodies and offers the opportunity to work in small scale to large scale product projects and to learn to utilize the (Enterprise Resource Planning) ERP database to track production schedules and deadlines and to enter production results. This position will also perform scale ups and perform troubleshooting of problematic products, including continuous improvement methodologies for efficiency. | 5/10/2019 |
| 15400 | BioLegend San Diego, CA Quality Control Associate - Custom Solutions Team BS/BA Exp: 1+ year in flow cytometry |
BioLegend is currently seeking a talented, detail-oriented Quality Control Associate to join our growing Custom Solutions Team. This position will be responsible for assisting with flow cytometry based QC testing, analysis, documentation, and will help maintain relevant databases. | 5/10/2019 |
| 15401 | BioLegend San Diego, CA Research Associate - ELISA BS/BA in immunology or biological sciences Exp: 1+ year in industry/lab |
BioLegend has an immediate opening for an ELISA Research Associate who will become an active member of our team who develop high quality ELISA products including proteins, antibodies and assay kits. The Research Associate will participate in all stages of the produce development process from product design, material sourcing, optimization, validation and product launch. | 5/10/2019 |
| 15402 | BioLegend San Diego, CA Quality Control Associate BS/BA in sciences Exp: 1 year in lab |
BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. This position will also perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. | 5/10/2019 |
| 15403 | BioLegend San Diego, CA Research Associate-Recombinant Protein BS or MS in biological sciences or related Exp: 1+ year in biotech or research |
This position is responsible for developing recombinant protein research products in the Molecular Cellular Immunology group by using cutting-edge synthetic biological technology. The duties include preparing buffer solutions and cell culture media, performing bacterial, insect, and mammalian cell expression, purifying recombinant proteins with chromatography, and performing molecular cloning, PCR, and DNA purification according to standard operating procedures. This position offers a significant opportunity for learning protein production techniques and career growth in biotechnology industry. | 5/10/2019 |
| 15404 | BioMarin Novato, CA Research Associate 1, Manufacturing Science and Technology MS in biological sciences, engineering, or chemistry Exp: 0-2 years |
This laboratory based position requires technical expertise in protein characterization and purification systems in support of ongoing manufacturing operations. He or she participates in monitoring and troubleshooting existing processes to build a detailed process understanding and developing process improvements consistent with cGMP. This position involves collaboration with process development, manufacturing, quality control, and quality assurance groups. Travel is limited to attending relevant professional conferences and workshops. | 5/10/2019 |
| 15405 | BioMarin Novato, CA Research Associate II, AAV Production (TEMPORARY) BS in biochemistry/molecular biology Exp: 1-4 years lab experience |
We are looking for highly motivated and hardworking Research Associate I/II for molecular biology and AAV production to coordinate and perform activities required to generate early stage material for the therapeutic programs at discovery stage. Responsibilities include: Operations of bench-scale bioreactor, Cell culture for insect and mammalian cell lines, Molecular cloning and PCR based quantitation | 5/10/2019 |
| 15406 | BioMarin San Frafael, CA Research Associate, BioAnalytical Testing I (TEMPORARY) BS/BA in biological sciences Exp: 0-2 years lab experience |
Responsible for efficient and effective laboratory operations, the Research Associate I has a significant impact on the company's ability to reach project goals in a timely manner with respect to delivery of data to support pre-clinical and clinical studies critical to advancing programs through the development process. The Research Associate I will perform bioanalysis, using validated PK or immunoassay methods, on non-clinical and clinical samples in a GLP compliant environment. Responsibilities can include sample preparation, sample analysis, GLP documentation, report generation, assay validation and troubleshooting, and interaction with BioMarin’s GLP quality assurance unit. | 5/10/2019 |
| 15407 | BioMarin Novato, CA Research Associate, Cell Culture Process Development MS in biological sciences Exp: 1+ years lab experience |
The Research Associate will be part of a stablished team of scientists and RAs working to develop and optimize AAV vectors production processes and assists team members in molecular biology and cell culturetasks including:Nucleic acid/plasmid purification. Cell propagation and plasmid transfection.Clone screening and selection. DNA analysis by agarose electrophoresis. PCR. DNA quantification by qPCR or ddPCR. etc | 5/10/2019 |
| 15408 | BioMarin Novato, CA Analyst, QC I (TEMPORARY) BS/BA in sciences Exp: 0-1 years lab experience |
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. Duties as an Analyst include: Perform, under direct supervision, chemical analyses of incoming raw materials under cGMP to meet specified timelines. Evaluate results and trend data. Maintain raw materials log and control of laboratory inventories. Maintain the laboratory in an inspection ready state. | 5/10/2019 |
| 15409 | Biomerieux Salt Lake City, UT Engineering Tech I AS/AA in engineering or related Exp: 0-4 years |
This technician works within a project team under the leadership of a more experienced individual such as a team lead, project lead, or project manager. The technician is expected to perform various types of technical activities including design, development, testing, verification, and documentation. This technician is expected to work and communicate well with other members and leadership of the team in order to meet the goals of the project. | 5/10/2019 |
| 15410 | Bio-Rad Hercules, CA Chemist I BS/BA in biological sciences Exp: 1-3 years |
The Chemist I will support the manufacturing of various reagents in Bio-Rad’s PCR product line. The Chemist will be expected to plan, prepare, and perform the manufacturing of reagents and consumable products. This position will interact with the planning, purchasing, and warehouse groups. | 5/10/2019 |
| 15411 | Bio-Rad Santa Rosa, CA Manufacturing Associate I HS Diploma Exp: 0-2 years |
Processes a variety of work orders associated with the manufacture of assays and other consumable reagent materials. The work orders consist of execution of a combination of tasks that include receipt and verification of issued materials, calibration of equipment, operation of equipment, coding of labels, sealing bags and pouches, dispensing of solutions, capping and torqueing of bottles, label application, assembly of components and kits, executing calculations and filling out required documentation such as work orders, procedures and logs. | 5/10/2019 |
| 15412 | Bio-Rad Hercules, CA Chemist I BS/BA in life sciences Exp: 0-2 years lab experience |
Bio-Rad Laboratories is seeking a chemist to support routine testing and logistical activities in the PCR Quality Control group. The incumbent will execute core laboratory testing involving qPCR, Real-Time PCR and droplet digital PCR, SDS-PAGE and other lab techniques. Other duties would include assisting with laboratory and general maintenance to support compliance to ISO13485 regulation standards. The incumbent will ensure adherence to documentation requirements and interact with peers and collaborating departments as needed. | 5/10/2019 |
| 15413 | Bio-Rad Hercules, CA Data Analyst I BS/BA in computer sciences or related Exp: 0-3 years |
This job may become a full time Data Analyst position with the Sales and Marketing team or the Customer Support team. We extract data from our Salesforce and SAP systems, transform that data into meaningful information, and load that data into our data lake to help drive sales. The Data Analyst is responsible for using a broad range of technologies, analytical techniques and methodologies in order to retrieve and analyze a broad range of data from various sources to provide predictive insights and support business decision making. | 5/10/2019 |
| 15414 | LGC Petaluma, CA R&D Research Associate BS/BA in chemistry or biology Exp: 1-2 years |
This position requires an individual with strong problem solving skills, good laboratory technique, and the ability to execute complex experiments. The successful candidate will have a desire to learn and the strong attention to detail. This position will entail running of automated oligonucleotide synthesizers as well as synthetic chemistry and/or molecular biology laboratory work to support new product development. | 5/10/2019 |
| 15415 | LGC Petaluma, CA Therapeutic Production Chemist BS/BA Exp: 1+ years |
The Therapeutic Production Chemist is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. The Therapeutic Production Chemist will work closely with experienced group members and may interact with other LGC facilities to support GMP activities, such as produce and release GMP batches. | 5/10/2019 |
| 15416 | Brooks Chelmsford, MA Mechanical Engineer MS Exp: 0-1 years |
Responsible for design/development, modification, and evaluation of primarily mechanical systems, equipment and packages. May contribute to total systems engineering, including other eng. disciplines. Conducts feasibility studies and tests new and modified designs. Is involved in all phases of development from initial concept to manufacturing. Directs support personnel in the preparation of detailed design, design testing and prototype fabrication. Provides design information to drafting for packaging documentation. Depending on level may function as a project engineer/leader with the resident responsibilities of proposals/project plan, schedules, work assignments, prime contact, technical presentations, cross functional issue resolution, etc. | 5/10/2019 |
| 15417 | BioAgilytix Durham, NC Sample Management Technician HS Diploma Exp: 1+ years in cGMP environment |
The Sample Management Technician is responsible for GxP-compliant processing of incoming and outgoing samples and reference materials. Responsible for GxP-compliant accessioning of incoming samples and reference material, as well as the outgoing shipment of samples, reagents and reference materials. Reviews study sample demographic data to confirm consistency between the tube labels, study paperwork and electronic sample management systems (eSMS). Resolves discrepancies, with responsibility for investigating and correcting sample anomalies identified in the eSMS system. | 5/5/2019 |
| 15418 | BioAssay Hayward, CA RESEARCH ASSOCIATE - ASSAY DEVELOPMENT BS/BA in biochemistry, chemistry, or biology Exp: 1-2 years lab experience |
We are currently looking for an enthusiastic research associate to join our R&D team. This position will entail developing novel assays kits and performing service projects. This candidate may also be involved in manufacturing or providing technical support to customers. | 5/5/2019 |
| 15419 | BioAssay Hayward, CA RESEARCH ASSOCIATE - MANUFACTURING BS/BA in biochemistry, chemistry, or biology Exp: 1-2 years lab experience |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing and packaging the finished products. This candidate may also join part time in our R&D team. | 5/5/2019 |
| 15420 | BioAssay Hayward, CA SALES ASSOCIATE HS Diploma Exp: 0-1 years |
The Sales Associate will be responsible for processing orders, preparing shipping documents, and keeping detail records. The individual will have to communicate with our customers by phone, fax and e-mail. The position will also involve packaging products for shipment. | 5/5/2019 |
| 15421 | Bioclinica Ocala, FL Medical Assistant HS Diploma Exp: 1+ years medical assistant |
Medical Assistant works in a clinic setting and handles basic clinical task and performs administrative/office duties. Interacts with patients and assist physician to ensure operations run smoothly and efficiently. Answer incoming calls, take messages and/or respond to all calls within 24 hours. Schedule patient appointments. Perform clinical task including but not limited to vital signs and height/weight; document medical history in patient charts. Prepare patient for examination. Ensure examination room is clean, well-equipped, and ready at all times | 5/5/2019 |
| 15422 | Bioclinica Orlando, FL Laboratory Assistant HS Diploma Exp: 1+ year lab experience |
The Laboratory Assistant must demonstrate knowledge of specimen collection and processing and handling requirements as relevant to Bioclinica Research and must have a thorough knowledge of lab procedures and practices. Maintain continuity of office operation. Perform blood draws, specimen collection, take vital signs, perform EKG testing and able to record accordingly. Effectively and professionally interact with patients, visitors, peers and other healthcare professionals. Timely specimen preparation for processing and shipping. Maintain laboratory inventory and ordering supplies. | 5/5/2019 |
| 15423 | Myriad Genetics Austin , TX RBM Software Engineer I BS/BA in computer sciences Exp: 0-2 years computer programing |
We are looking for a Software Engineer I candidate to work within the broader Informatics team who will use their computer programming skills to develop solutions for the company’s lab operations and other business needs. You will be expected to collaborate with other departments throughout the development lifecycle from planning thru acceptance testing. Ressponsibilities include: Responsible for developing and testing of computer programs, databases and spreadsheets. Collaborate with team members to determine requirements and participate in design discussions. Display ownership and responsibility for the projects you work on. | 5/3/2019 |
| 15424 | Myriad Genetics Austin , TX RBM Laboratory Technician - Testing BS/BA in sciences/biomedical engineering Exp: 0-3 years |
The goal of the Lab Technician I is to ensure that process’s required for a production run as it pertains to samples and reagents are done in an organized and expedient manner. The Technician is accountable for following company procedures and working to the best of their ability to ensure quality in all aspects of the job. Responsibilities include: Processing of biological samples required for production runs, including locating and verifying sample identification, thawing, mixing, and centrifugation. Transferring samples to the production sample plate in a manner that maintains the integrity of the sample identity, and accurately pipetting the amount of sample required for the run, etc. | 5/3/2019 |
| 15425 | Myriad Genetics Salt Lake City, UT Clinical Research Associate I BS/BA in sciences Exp: 1+ years in clinical research |
Under the direction of the Program Manager and Clinical Trial Manager, the Clinical Research Associate I contributes to the tactical implementation and conduct of clinical research studies. The CRA I ensures the quality of each research study through on-site and centralized monitoring of protocol and regulatory compliance. The CRA I represents Myriad at the research site level and maintains collaborative relationships with investigator sites and the internal clinical development team. This position can be based in Salt Lake city, Utah or Mason, Ohio. | 5/3/2019 |
| 15426 | Astellas Seattle, WA Research Associate 2, Cell Editing MS Exp: 0-2 years lab experience |
The Cell Editing RA 2 will work as part of a team evaluating, planning, and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. Will assist with complex laboratory operations and take on more responsibility to provide content for various documents and reports. Will be able to execute protocols with minimal guidance, and the ability to summarize results independently. | 5/3/2019 |
| 15427 | Astellas Seattle, WA Research Associate 2, Process Developmen MS Exp: 0-2 years lab experience |
The Process Development Research Associate 2 will work as part of a team evaluating processes, and planning/executing experiments to improve all aspects of culturing, gene-editing, and engineering of pluripotent stem cells. The Research Associate 2 will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. Will assist with complex laboratory operations and take on more responsibility to provide content for various documents and reports. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. | 5/3/2019 |
| 15428 | Atex Carlsbad, CA Biomechanical Testing Engineer BS or MS in mechanical/biomedical engineering Exp: 1-2 years in med devices |
Responsibilities as a testing engineer include; Performs mechanical tests according to recognized standards and internal policies and procedures. Compiles, critically analyzes and interprets test data. Prepares clear, complete and accurate technical engineering documentation. Assists with the calibration, safety, maintenance, and efficient utilization of testing equipment. Designs and oversees fabrication of test fixtures as needed. Provides technical support to other department (e.g., R&D, Regulatory, Marketing, Sales). Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. | 5/3/2019 |
| 15429 | Atreca South San Francisco, CA Research Associate, Target Biology BS in molecular biology/biochemistry Exp: 1-6 years |
In this position, the successful candidate will apply their skills and expertise in protein biochemistry to identify targets bound by patient derived antibodies using protein biochemistry and molecular biology techniques. These include protein and carbohydrate arrays, immunoprecipitation, and other protein biochemistry techniques. Responsibilities include: Perform immunoprecipitation and array screening of antibodies selected for testing in in-vivo tumor models. Generate lysates and subcellular fractions from tissue culture cells (including radiolabeled cells) and mouse tumors. Perform pilot immunoprecipitation screens on lysates from tumors and radiolabeled cells. | 5/3/2019 |
| 15430 | Atreca Redwood City, CA Research Associate - FACS (Temporary to FTE) BS/BA in biology or related Exp: 1+ years research in cell biology |
In this position, a successful candidate will apply her/his skills in biology and flow cytometry to Atreca’s Immune Repertoire Capture™ technology. The RA will isolate peripheral blood mononuclear cells (PBMCs), isolate various B and T cells and sort them into microplates in a biosafety level 2 (BSL2) environment. The RA will work in a collaborative environment in the team. Responsibilities include: Isolate peripheral blood mononuclear cells from human blood. Freeze/thaw and stain PBMCs or primary tissues. Sort cells into microplates through Fluorescent-Activated Cell Sorting (FACS). Follow laboratory safety guidelines and practices. | 5/3/2019 |
| 15431 | Atricure Cincinnati, OH Associate Process Engineer BS/BA Exp: 0-7 years |
The Associate Process Engineer is responsible for on-going production, validations, and continuous improvement of new and existing manufacturing processes. He/she contributes in a creative and collaborative ways to achieve the company’s goals of producing market leading products through positive patient outcomes. Responsibilities include: Team member of projects involving design, manufacturing, and quality resources, both internal and external. Knowledge of general manufacturing technologies (plastic injection molding, stamping, milling, turning, assembly methods, various fastening techniques) including low to medium volume manufacturing processes. Able to define, communicate, and develop fixture concepts using internal and external resources. Able to incorporate the capabilities of typical production association into these concepts | 5/3/2019 |
| 15432 | Atricure Cincinnati, OH Associate Manufacturing Engineer BS/BA Exp: 0-7 years |
The Associate Manufacturing Engineer is responsible for the development, qualification, verification and validation of manufacturing processes. The Associate Manufacturing Engineer will contribute in creative and collaborative ways to achieve the company’s goals of producing market leading products through positive patient outcomes. Responsibilities include: Review of component designs and identification of Design for Manufacturing opportunities. Work with outside suppliers to define, document, analyze and qualify their manufacturing processes. Able to define, communicate, and develop fixture concepts using internal and external resources.Able to incorporate the capabilities of typical production association into these concepts | 5/3/2019 |
| 15433 | ATUM Newark, CA Production Associate - Synthetic Biology Manufacturing BS/BA in biology or related Exp: Entry Level |
This entry-level position is within our production group. The work includes following standard operating procedures for using automated liquid handling stations, interfacing with our in-house database, providing support in various lab functions including PCR, making agarose gels, growing culture from stock, organizing/purging storage plates, and interacting with our bioinformatics department. | 5/3/2019 |
| 15434 | Avedro Burlington, MA Associate Research Formulation Scientist MS or BS in biochemistry, analytical chemistry, etc Exp: 0-2 years |
Avedro is seeking a highly motivated and versatile individual to join our R+D team as an Associate Formulation Scientist. In this role you will be responsible for assisting with the formulation development and testing efforts within our ocular drug development program. Located primarily at our labs in Burlington, MA and interfacing with other group members in our Waltham, MA offices, you will join a growing dynamic team of interdisciplinary scientists at a world leading company on the forefront of corneal crosslinking science. | 5/3/2019 |
| 15435 | Avion Pharmaceuticals Austin , TX Pharmaceutical Sales Representative BS/BA Exp: 1 year of business/pharma sales |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’s offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. | 5/3/2019 |
| 15436 | Avion Pharmaceuticals Worcester, MA Pharmaceutical Sales Representative BS/BA Exp: 1 year of business/pharma sales |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’s offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. | 5/3/2019 |
| 15437 | Avomeen Analytical Services Ann Arbor, MI SAMPLE COORDINATOR BS/BA in chemistry Exp: Entry Level |
This is an entry level position in a chemistry-based contract research organization. A background in the sciences, particularly chemistry, is preferred. Responsibilities include; Reporting to the Manager of Quality, responsible for logging in samples and chemicals for use in the laboratory. Keep chemical inventory program up to date. Keep chemical storage areas free of expired chemicals and uncluttered. Ensure chemicals in the laboratory are in the correct locations. Ensure glassware is in properly labeled locations | 5/3/2019 |
| 15438 | Axsome New York, NY Clinical Trials Assistant BS in biological/physical sciences Exp: 1 years in clinical environment |
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. | 5/3/2019 |
| 15439 | Bausch Health O'Fallon, MO Manufacturing Associate I HS Diploma Exp: 0-1 years |
Perform tasks within full-scale production manufacturing operations, including routine assembly; or quality assurance and reliability testing following established methods and procedures. Operators are to be cross-trained and expected to perform any/all essential tasks within the production/manufacturing operations within the standard run time associated with each assembly. Use of basic hand tools. | 5/3/2019 |
| 15440 | Bausch Health Lynchburg, VA Distribution Associate I HS Diploma Exp: 0-1 years |
The Distribution Associate I is responsible for performing the following: As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader. | 5/3/2019 |
| 15441 | Bausch Health Lynchburg, VA Distribution Associate I HS Diploma Exp: 0-1 years |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and/or group leader. This position is third shift, Sunday-Thursday | 5/3/2019 |
| 15442 | Baxter Aibonito, PR Engineer I BA/BS in mechanical/industrial/chemical engineering Exp: 0-2 years |
Must be bilingual (English and Spanish). Responsibilites include: Provide technical support to Manufacturing, Engineering and Quality areas. Improve manufacturing processes. Participate on the evaluation of customer complaints and provide suggestions for process/product improvements. Generate validation protocols and reports for the qualification of process equipments or process changes. Develop and update standard operating procedures for new and existing processes and equipment. | 5/3/2019 |
| 15443 | Baxter Marion, NC Quality Lab Assoc I Chemistry (8th Shift- 7PM-7AM) BS/BA in micro biology/biological sciences Exp: 0-2 years |
Duties and responsibilities include: Conduct critical chemical and physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities. Work under minimum supervision. Use sophisticated laboratory instrumentation and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles. Complete all testing, including special project / protocol testing in a timely and appropriate manner. Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations. | 5/3/2019 |
| 15444 | Baxter Marion, NC Quality Laboratory Associate I – Microbial ID BS/BA in microbiology/biological sciences Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. Essential Duties and Responsibilities include: Operate lab equipment such as laminar flow hoods, autoclave, incubators, and other equipment. Read plates and enter test results and other data into LIMS. Initiate paperwork for microbial out of limit investigations and provide needed information to Investigators. Perform monthly safety audits | 5/3/2019 |
| 15445 | Baxter Cleveland, MS Engineer I BS in engineering Exp: 0-2 years engineering/manfacturing |
This position is a key role in Maintenance in our Manufacturing Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support working within the Operations Group and Engineering. Cross-functional project management will be involved in this role as well. Duties include: Design/modify precision assembly and/or manufacturing equipment. Manage multiple projects with minimal supervision. Prepare estimates for various tasks and projects. Manage capital projects both directly and through coordinating engineers. | 5/3/2019 |
| 15446 | Baxter Medina, NY Quality Engineer-Investigations BS in engineering Exp: 1-3 years of medical device experiences |
This position has primary responsibility for investigation, review, and completion of all Quality Engineering complaint issue analysis tasks utilizing various quality system inputs. Responsibilities include: Review individual complaints and associated service data to determine risk level and complete investigation into the “as “determined” problem code and cause codes for each complaints. Analyze data from various quality inputs (including but not limited to : Field Corrective Action (FCA), Complaints, FDA Medical Device Reports (MDR), etc.) to determining trends and systemic issues. Prepare and issue reports based on information analysis. Review existing investigation reports and identify gaps for GMP compliance. Develop strategies and plans to close the gaps in an efficient and technical manner. | 5/3/2019 |
| 15447 | Baxter Round Lake, IL Associate Regulatory Affairs-R&D BS/BA in sciences/pharmacy Exp: 0-2 years |
Under general supervision responsible for the coordination and the preparation of documents/packages for regulatory submissions. Review and evaluate technical and scientific data and reports required for submission in support of Baxter’s products. Responsibilities include: Track of status and progress of regulatory documentation. Review, edit and proofread regulatory documentation. Assist in preparation and review of labeling, SOP’s, and other departmental documents. Compile under supervision regulatory documents for submission | 5/3/2019 |
| 15448 | Baxter Round Lake, IL Engineer II BS in engineering Exp: 1-3 years |
Responsibilities as Engineer II include: With supervision, perform standard engineering assignments which are typically a significant portion of a larger project. Lead small project teams through the planning, execution, and completion of smaller projects or defined pieces of larger projects. With supervision, lead projects within Baxter’s change control management process, from initiation through closure. Change Owners assign and prepare impact assessments, develop change plans, write and execute engineering studies, while working closely with manufacturing plants, quality, regulatory, purchasing, and various scientific/technical groups. | 5/3/2019 |
| 15449 | Bayer West Sacramento, CA Data Engineering Graduate Scholar MS in computer science, chemistry, statistics, or related Exp: 1+ years |
The primary responsibilities of this role, Data Engineering Graduate Scholar, are to: Design and develop pipelines to connect external data sources to a data lake in a collaborative effort with Bayer R&D IT and Bayer Biologics; Design and develop workflows to link datasets in the data lake based on shared ontologies; Design and develop REST APIs and web-based UIs to provide access to linked datasets in the data store; Gain expertise in frameworks for schema discovery from schema free sources and use expertise gained to extract knowledge from existing schema-free sources; Design and develop workflows to link datasets in the data lake based on shared ontologies; | 5/3/2019 |
| 15450 | Bayer Multiple Locations, US Graduate Scholar, Medical Affairs MS in computer science, chemistry, statistics, or related Exp: 1+ years |
The position will allow someone who has completed advanced studies in a science or engineering field or a physician to work closely with the radiologists, engineers and physicists at Bayer and take on a project that supports the use of contrast enhanced imaging and associated informatics software. They will be able to understand what the scientists and physicians do in Radiology at Bayer through an in-depth project. A specific project that fits their background and training will be assigned. Projects typically involve the investigation of improvements to imaging in radiology. They involve programming, data analysis and innovative thinking. They may also help develop scientific materials for presentations and help answer scientific questions internally and externally with collaborators or customers. | 5/3/2019 |
| 15451 | Beam Therapeutics Cambridge, MA Research Associate, RNA editing & Novel CRISPR nucleases BS or MS in biological sciences Exp: 1+ years of research |
he ideal candidate will support efforts in developing next-generation RNA base editing technologies as well as exploration of novel CRISPR nucleases for enhancing our base editing tool-box. Experience with molecular biology techniques and mammalian cell culture is required. Responsibilities include: Molecular biology support: Vector and primer design, cloning, PCR, DNA/RNA isolation, Sanger sequencing analysis, plasmid preparation, etc. NGS sample preparation. Mammalian cell culture and non-viral transfection. Yeast cell culture. Data analysis and visualization to determine gene editing outcomes. | 5/3/2019 |
| 15452 | BD Woburn, MA Manufacturing Engineer I BS in engineering (chemical engineering preferred Exp: 1-3 years in manufacturing |
This position is responsible for coordinating and providing engineering support throughout the manufacturing facility in areas such as process improvements, technological advancements, cost improvements, facility maintenance, safety, and environmental regulation. Essential job functions include: Coordinate and participate in plant CIP and process improvement programs as required. Support, or lead as required, activities such as failure investigation, design of experiments, process capability studies, qualifications, and validations of processes and equipment. Coordinate tactical plans geared towards timely completion of line extensions and major equipment installations, modifications, or enhancements. | 5/3/2019 |
| 15453 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I BS/BA in engineering or STEM field Exp: |
As a Quality Engineer I, you will learn and develop skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. Responsibilities include: Conduct experiments to prove hypotheses. Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques. Design engineering test protocols and use a data-driven approach to collect, analyze and summarize data into engineering reports. Perform root cause investigations for design and manufacturing | 5/2/2019 |
| 15454 | Applied Medical Rancho Santa Margarita, CA Associate Customer Relations Representative BS/BA Exp: 1-2 years customer service |
As an Associate Customer Relations Representative, you will be responsible for working within the framework of a team and performing the following activities: Enter customer orders and understand the Customer Relations department’s processes. Comprehend and comply with safety rules and company policies. Work directly with external customers as well as Applied Medical internal departments such as Credit, Field Operations, Shipping, etc. Assist with other tasks and projects as needed | 5/2/2019 |
| 15455 | Applied Medical Rancho Santa Margarita, CA Corporate Communications Associate BS/BA in communications, english, or related Exp: 1+ years in corporate communications |
As a Corporate Communications Associate, you will work on a wide variety of projects that help to communicate the company’s brand, purpose and programs to both internal and external audiences. You will be responsible for working within the framework of a team and performing the following activities: Edit and proofread a variety of communication materials, primarily for in-house teams and other internal programs. Build relationships within various internal departments to best understand each team and help identify communication needs and opportunities. Create posts and provide content support to community managers for the company’s social media platforms including Facebook, Twitter, YouTube and LinkedIn | 5/2/2019 |
| 15456 | Applied Medical Technologies Brecksville, OH Mold Process Engineer AS/AA in plastics/plastic technologies Exp: 1-4 years |
This list is not comprehensive but meant to represent the most common or important duties of the position. Develop, document and implement standard molding processes and methodologies. Use scientific molding method to validate new molding processes and re-validate existing/legacy molds. Research, design and develop manufacturing processes and new technologies. Participate in Tool Design Reviews and recommend improvements to optimize molding, setup, and overall manufacturing. Work with design, manufacturing, production, engineers and tooling during the entire development cycle. Emphasis on new mold sampling prior to transfer to production. Research, develop and implement manufacturing process controls, machinery modifications and improvements. | 5/2/2019 |
| 15457 | Applied Stem Cell Milpitas, CA Document Control Specialist BS/BA in literature/english Exp: 1 years in document control |
Duties include: Write, revise and review SOPs. Track and control document flow. Achieve manufacturing and quality records. Ensure auditing and manufacturing documentation is kept up to date. Maintenance of Quality Assurance documentation. Train Production staff training on quality procedures, protocols, and documentation | 5/2/2019 |
| 15458 | Applied Stem Cell Milpitas, CA Research Associate, Cell Biology (iPSCs) BS or MS in biological sciences Exp: 1-2 years lab experience |
This is a hands-on lab-based role in Induced Pluripotent Stem Cells (iPSCs) group with a focus on iPSC genome engineering and differentiation using ASC’s gene editing technologies. Responsibilities include: Work closely with a multi-function team to deliver engineered iPSCs cell lines and a variety of other cell types. Work on gene editing projects in iPSCs/stem cells, preparing reagents, performing cell culture and cell-based assays. Work on iPSCs generation, differentiation and characterization. Apply scientific knowledge, critical thinking, and problem-solving abilities to troubleshoot and refine methods and assays. Interpret genotyping data from Sanger sequencing and Nextgen sequencing | 5/2/2019 |
| 15459 | Aptar Pharma Congers, NY Microbiology Technician BS in microbiology or biological sciences Exp: 1-3 years in cGMP lab |
The Microbiology Technician supports Injectable manufacturing at Congers. The Technician performs duties as needed related to environmental monitoring in the pump manufacturing facility and assists in the technical and quality efforts in the lab. Responsibilities include: Perform microbiology & particulate testing of product and processes (clean room, WFI loop) by accurately following all testing as specified by the appropriate quality documentation. Perform environmental monitoring in manufacturing areas, including tracking & trending test results and performing bioburden sampling in controlled areas. Assist in investigations related to Lab OOS (Out of Specification) and support Production OOS investigations. | 5/2/2019 |
| 15460 | Aptar Pharma Congers, NY Plastics Process Technician HS Diploma Exp: 1-3 years working in manufacturing |
The primary mission of our Technicians is to operate injection molding equipment to successfully meet production demands and quality standards. Duties include but are not limited to: Utilize your mechanical skills to install, remove and adjust Injection Molding machinery and equipment. Troubleshoot Injection Molding machines, follow process to resolve failures, other problems. Coordinates and sets up machines, robots and other equipment performing necessary tests to ensure company compliance. Trains employees in the correct procedures for operation as needed. Assist in preventative maintenance and repair of molding machines, molds and peripherals (robots). | 5/2/2019 |
| 15461 | Evotec Brandford, On Lab Technician BS in sciences Exp: 1-2 years |
The purpose of this position is to perform laboratory processing of client orders; the majority of which will involve manual weighing and liquid handling of compounds. The position requires a highly motivated individual, able to work independently and as part of a team to ensure successful project support. This role will be expected to have increased understanding of Compound Management workflows, set forth SOPs, etc. Tasks will include, but are not limited to, performing the day to day laboratory work and direct communication with local and remote lab colleagues in a cross-functional environment. | 5/2/2019 |
| 15462 | Arbor Cambridge, MA Research Associate (Bioengineer) BS or MS in biological sciences Exp: 0-5 years |
At Arbor, Research Associate Bioengineers use a combination of molecular biology, high-throughput techniques, and next-generation sequencing to systematically search through nature’s gene diversity to discover and engineer new protein technologies. In this interdisciplinary position, you will be expected to perform high-throughput functional screening to further Arbor’s mission of biodiscovery, and accelerate the company’s platform technologies through protocol development and testing. | 5/2/2019 |
| 15463 | Arbor Cambridge, MA Software Engineer - Infrastructure BS or MS in software engineering Exp: 1-2 years |
On the Software Engineering Infrastructure team, you will apply your expertise in Python and large scale distributed systems, building data processing pipelines and interactive tools. | 5/2/2019 |
| 15464 | Arbor Cambridge, MA Research Associate (Assay Development) BS or MS in biochemistry, molecular biology or related Exp: 1-3 years lab experience |
The ideal candidate will have significant research or industrial experience in protein purification, assay development and optimization. They will also possess a strong background in molecular biology, excellent organizational skills and attention to detail, as well as a strong desire to learn and the ability to work independently. Responsibilities include: Routinely perform the established assays. Optimization of assays to increase throughput and performance . Document, compile, and analyze experimental data. etc | 5/2/2019 |
| 15465 | ArcherDX Boulder, CO cGMP Manufacturing Associate II BS in physical/biological sciences Exp: 1-2 years |
Associate level position for manufacturing medical devices in accordance with controlled procedures (SOPs) in compliance with Good Manufacturing Practice (GMP) regulations and current GMP (cGMP) guidelines. Manufactures solutions, labels and fills containers, labels and assembles kits. Compiles auditable electronic or paper records of manufacturing, maintains equipment logs and monitors supplies. Manufacture product as specified in controlled manufacturing procedures, and in compliance with cGMP regulations and guidelines. Accurately complete documentation in cGMP manufacturing batch records, using Good Documentation Practices | 5/2/2019 |
| 15466 | Arcus Biosciences Hayward, CA QB2-Research Associate BS or MS in biology/biochemistry Exp: 0-3 years |
The job requires the application of creative problem-solving approaches to the execution of new biochemical and cell-based assays. Responsibilities include, but are not limited to: Performing routine assays to support chemistry efforts. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro assays. Contribute during lab meetings and assist in the analysis and reporting of experimental data to project teams. | 5/2/2019 |
| 15467 | Arcus Biosciences Hayward, CA QB1-Research Associate BS or MS in biological sciences Exp: 0-3 years |
The job requires the application of creative problem-solving approaches to the execution of new biochemical and cell-based assays. The successful candidate will have excellent practical laboratory skills, coupled with aptitude and enthusiasm for automated laboratory assay techniques. Responsibilities include, but are not limited to: Transient and stable mammalian cell protein expression. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro assays. | 5/2/2019 |
| 15468 | Arcus Biosciences Hayward, CA Research Associate II MS Exp: 0 years drug discovery |
The Biology group is seeking a self-motivated, collaborative and highly skilled individual who wishes to play a key role in advancing novel immunotherapy drug candidates from the discovery phase into the clinic. The data generated by the in-vivo team is central to advancing our understanding of the mechanism of action of our drug candidates and potential combination partners. Specific responsibilities will include collaborating with the project team to conduct tumor efficacy studies in both syngeneic and xenograft models. In addition to taking point on in-vivo efficacy studies the successful candidate will be involved in the ex-vivo analysis of tumor samples. Additional duties could also include in-vitro responsibilities such as the maintenance and preparation of cell lines for tumor studies. | 5/2/2019 |
| 15469 | Arcus Biosciences Hayward, CA Research Associate: Quantitative Biology BS or MS in molecular biology/biochemistry Exp: 0-3 years |
The successful candidate will have strong organizational skills and attention to detail, coupled with excellent practical laboratory skills, and aptitude and enthusiasm for automated laboratory assay techniques. Responsibilities include, but are not limited to: Mammalian cell culture. Biological sample banking. Biology and tissue culture lab management, safety program support. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro assays. | 5/2/2019 |
| 15470 | Ardelyx Fremont, CA QA Specialist I BS in sciences/engineering Exp: 1-7 years in quality |
This role will be responsible for QA oversight of all GxP Computer Systems. The incumbent, working with the functional teams must ensure that all GxP regulated systems are purchased, audited, installed and maintained based on industry best practices (e.g. GAMP5) and regulatory requirements (e.g. 21CFR Part 11 and relevant FDA Guidance). The position plans and organizes all QA activities for computer system validation projects. Duties include, but are not limited to, oversight and approval of validation - related documents, leading risk assessments and working with project team to determine which elements should be validated, conducting and/or coordinating impact assessments of proposed changes to computerized systems and leading inspection (external/internal) readiness activities related to computer system validation. The candidate will ensure that all GxP computer systems are maintained in a validated state in addition to designing work processes for users and administrators of the aforementioned systems. | 5/2/2019 |
| 15471 | Arkray Minneapolis, MN Laboratory Assistant 1 HS Diploma Exp: 1+ years in clinical lab |
ARKRAY is currently seeking a Laboratory Assistant to perform laboratory testing, data entry, support evaluation studies for quality testing, complaint investigations, and support ARKRAY products. Responsibilities include: Performs laboratory testing and assists in clinical studies to meet QS specifications and to support Operations and D&S activities. Prepares samples for product evaluation including blood, urine, and saliva. Maintains documentation in compliance with applicable regulatory programs. Perform computer entry of data. | 5/2/2019 |
| 15472 | Array Biopharma Boulder, CO Cell Culture Biologist BS or MS in life sciences Exp: 1+ years maintaining cell culture |
We are seeking a highly motivated Cell Culture Biologist with excellent organizational, problem solving, and communication skills to join our Structural Biology group located in Boulder, Colorado. This scientist will be responsible for maintaining and scaling up (≥5L) insect cell and E. coli cultures in suspension for recombinant protein expressions. The individual will also be involved in molecular cloning and construct design. A track record of excellent aseptic techniques and experience in molecular biology and protein expression are essential for this role. | 5/2/2019 |
| 15473 | Array Biopharma Boulder, CO esearch Associate / Associate Scientist - Medicinal Chemistry MS in organic chemistry Exp: 0-2 years |
The ideal candidate will have ability to work closely with others in a collaborative manner. Responsibilities include: Demonstrates technical competency in reaction set-up, product isolation, purification and analysis, from milligram to multigram scale. Work efficiently with minimal supervision in the lab. Adhere to all safety requirements. Develop an understanding of SAR, contribute to analog design. Collaborate closely with colleagues to discuss data and generate new ideas. Demonstrate curiosity and interest in furthering knowledge of drug discovery. | 5/2/2019 |
| 15474 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, CMC BS or MS in chemistry/biochemistry Exp: 0-3 years lab experience |
This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates. The successful candidate will be expected to: Perform solid-phase synthesis and purification of oligonucleotide drug candidates. Analyze small-molecule and macromolecular targets using standard methods, such as HPLC, UV-Vis spectrophotometry, mass spectrometry, NMR, etc. Track progress against project timelines, generate regular status updates, and communicate progress and issues to management, including presentation of findings at team meetings | 5/2/2019 |
| 15475 | Arthrex Ave Maria, FL Quality Control Inspector I HS Diploma Exp: 1+ years in QC |
The QC Inspector will perform a variety of quality control test and inspection functions on materials, components and finished goods at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products. Responsibilities include: Performs and documents dimensional inspections on inventory parts using engineering prints, Inspection procedures or work instructions. Selects products at specified stages in the production process, if applicable, and inspects products for variety of qualities, such as dimensions and functionality. Detects non-conformances during production operations effectively. | 5/2/2019 |
| 15476 | Arthrex Ave Maria, FL Automation Engineer I BS in mechanical/electrical engineering Exp: 1-2 years |
We are actively seeking an Automation Engineer I to provide automation and equipment development and support expertise to the Final Device Assembly and Packaging engineering group. This engineer will be a resource for all activities required to build, program, install, debug, and implement automated equipment. The successful candidate will have strong communication and analytical skills, knowledge of manufacturing process and a Bachelor’s degree in Engineering or Engineering Technology. | 5/2/2019 |
| 15477 | Ambry Genetics Aliso Viejo, CA Research Associate I BS or MS in life sciences Exp: 0-2 years lab experience |
Research Associate I is responsible for assisting senior R&D staffs to design, develop, and validate clinical diagnostic assays spanning a wide range of Next-Generation sequencing and microarray technologies. Duties include: Aid in the design and development of clinical diagnostic assays for use in a CLIA/CAP regulated setting. Participate in drafting Standard Operating Procedures for new assays. Perform research experiments, such as primer design and preparation, PCR, electrophoresis, gel imaging and analysis, Sanger Sequencing, Next-Gen sequencing library preparation, aCGH microarray labeling, and sequencing analysis. | 4/29/2019 |
| 15478 | Ambry Genetics Aliso Viejo, CA Research Associate I - ATG Lab BS or MS in life sciences Exp: 0-2 years lab experience |
The Research Associate I is responsible for assisting senior ATG Lab staff to design and perform research diagnostic assays spanning a wide range of PCR and Next-Generation sequencing technologies. Perform research experiments, such as primer design and preparation, PCR, electrophoresis, gel imaging and analysis, Sanger Sequencing, Next-Gen sequencing library preparation, and sequencing analysis. Aid in the design and development of diagnostic assays for use in a CLIA/CAP regulated setting. Participate in drafting Standard Operating Procedures for new assays. | 4/29/2019 |
| 15479 | Ambry Genetics Aliso Viejo, CA Lab Assistant, Quality Control HS Diploma/GED Exp: 0-1 years (entry level) |
As a Lab Assistant under our Quality Control (QC) team, you will be overseeing Clinical Lab Quality Control, including equipment maintenance and reagent QC support. Responsibilities include: Oversee equipment preventative maintenance/routine maintenance and systems, as well as driving routine multi-system testing. Manage general temperature & humidity monitoring. Supervising general reagent quality control and systems. Regularly communicate with vendors/suppliers and coordinate on-site maintenance or repairs. Maintain current knowledge of reagent stability and storage, proper handling of reagents, and associated safety protocols. Maintain laboratory safety by ensuring work area is safe and clean, noting any problems that may require prompt and proper repair. | 4/29/2019 |
| 15480 | Ambry Genetics Aliso Viejo, CA Quality Assurance Engineer BS/BA in computer sciences Exp: 0-2 years in software QA |
You will be working in a team that is handling one or two applications. You will be getting requirements from a QA manager and will be with the QA development team. You are responsible for the documentation, development and execution of basic manual test cases. You will also be working with the application development team for creating data sets for testing, debugging issues, and improving products. Your end users are mostly internal and need to be able to support them when necessary. | 4/29/2019 |
| 15481 | Ambry Genetics Aliso Viejo, CA Clinical Assistant I BS/BA Exp: 0-2 years |
The clinical assistant I will provide support and help organize work flow for the genetic counselors, laboratory directors, and medical directors in the clinical diagnostics department. He or she will also share some general responsibilities of the Client Services department, such as providing testing information to clients about our products and services, patient test status, and routing calls throughout the organization as needed. Providing detailed information (technical and clinical) about genetic tests offered by Ambry Genetics, communication of relevant results, and basic results interpretation, if necessary. Work collaboratively with the Clinical Diagnostics team, laboratory personnel, accessioning department and sales & marketing department to make sure the needs of our clients are met. | 4/29/2019 |
| 15482 | Ambu Noblesville, IN CAD CAM Engineer AS or BS/BA in engineering Exp: 0-2 years |
Responsibilities include: Draw and design parts, fixtures, tooling and test equipment. Write programs for CNC machines and support the tool room in the manufacture of designs. Update all modifications to part prints and 3D data. Measure and determine proper machine function for finial sizing of components. Create new designs for products, production machinery, injection molds, and mold shop tooling and fixturing. etc | 4/29/2019 |
| 15483 | Ambu Noblesville, IN Quality Assurance Inspector - 2nd and 3rd Shift HS Diploma/GED Exp: 1-3 months |
Monitor compliance to in-house standard operating procedures (SOP's) and Current Good Manufacturing Practices (CGMP's), pertaining to the manufacturing, packaging, storage, and distribution of finished product. Inspect and test components, labeling, sub-assemblies and finished product for conformance to all written specifications. Ensure complete, accurate, and proper performance of all QA functions, including documentation. Monitor all processing steps to ensure conformance to Manufacturing specifications (work order) and processing methods. Assist in verifying the complete, accurate and proper performance of all Quality Assurance functions, including documentation to ensure compliance with CGMP's, and ISO 9001, MDD, EN46001, production and corporate standards. | 4/29/2019 |
| 15484 | Amgen Thousand Oaks, CA Bioprocess Development Sr. Associate MS Exp: 0-2 years |
The successful candidate will be responsible for support of the development, characterization, scale-up and support of upstream and downstream processes to enable clinical advancement of Amgen programs. The successful candidate will design and execute experiments at the bench scale, spanning the end-to-end drug substance process, including both cell culture and purification operations. The candidate will apply established platform approaches and utilize problem-solving skills to rapidly solve day-to-day experimental challenges. Additionally, the candidate will utilize out-of-the-box thinking to contribute to technology development. | 4/29/2019 |
| 15485 | Amgen Thousand Oaks, CA Associate Manufacturing BS/BA Exp: 0-4 years |
This Cell Culture Manufacturing Associate position will support the on going commercial operations for drug substance intermediate and the start-up of new clinical and commercial drug substance manufacturing operation in Thousand Oaks, CA. The Associate will execute production operations on the manufacturing floor including execution and coordination of commissioning and qualification of process equipment. This role will interface between the GMP manufacturing teams in the plant and our partner organizations. | 4/29/2019 |
| 15486 | Amgen Rhode Island, RI Associate Manufacturing BS/BA Exp: Graduation by June 2019 |
Under general supervision, Associate Manufacturing will perform operations in the Manufacturing area, specifically Purification processes. Operations will be performed according to Standard Operating Procedures (SOPs). Associate will perform and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams and represent the Purification group. Associate may also have the responsibility of owning NC/CAPA’s and Change Control records. In addition, Associate may identify, recommend, and implement improvements related to routine functions. | 4/29/2019 |
| 15487 | Amgen Thousand Oaks, CA Associate Scientist MS in life sciences or engineering Exp: 0-2 years |
The Associate Scientist’s responsibilities include, but are not limited to, the following: Design and execute experiments for analytical support of biotherapeutic proteins using HPLC, LCMS, and capillary electrophoresis. Develop and optimize analytical methods. Troubleshoot and maintain analytical equipment in good working order. Analyze and clearly document experiments in Electronic Lab Notebook (ELN). | 4/29/2019 |
| 15488 | Amicus Greater Philadelphia, PA Research Associate, Discovery Biology AS/BS in sciences Exp: 0-2 years lab experience |
The Research Associate position will be responsible for supporting lab operations in the purification of target proteins and bio-reagents. Responsibilities include: Performing experiments for the bench scale purification of protein therapeutics and reagents. Performing necessary assays in support of both upstream and downstream activities. Supporting therapeutic protein drug substance process development and scale up. Evaluating technologies to improve downstream processes. Serving on departmental, interdepartmental, and project teams. | 4/29/2019 |
| 15489 | Amicus Cranbury, NJ Clinical Trial Associate BS/BA Exp: 1+ year in clinical trial operation |
The Clinical Trial Associate is responsible for assisting the Clinical Operations team(s) to provide efficient execution of assigned studies, including appropriate filing of all documentation. Responsibilities include: Assist with documents during study start-up including CDAs and CTAs. Assist with compilation of regulatory documents. Coordinate investigator payments for studies where the Sponsor is responsible for this activity. Verify investigator payment details submitted for payment by CROs for studies where CROs are responsible for this activity. etc. | 4/29/2019 |
| 15490 | Amicus Greater Philadelphia, PA Associate Scientist, Protein Expression Analysis - Gene Therapy MS in sciences Exp: 0-2 years lab experience |
This position will be responsible for the transfection or transduction of gene therapy-related constructs for the characterization of protein expression efficiency and protein product characteristics across a wide range of therapeutic targets. Duties include: Maintenance of the appropriate cell systems for evaluation of protein expression. Transfection or transduction of transgene constructs into an appropriate cell system to evaluate protein expression and characteristics. Measurement of protein expression level and quality. Tracking progress of multiple protein expression projects and prioritization of parallel projects to ensure timely delivery. | 4/29/2019 |
| 15491 | Amicus Greater Philadelphia, PA Associate Scientist, Bio-reagent Development MS in sciences Exp: 0-2 years lab experience |
This position will be responsible for the expression and purification of enzymes and antibodies required as bio-reagents for the evaluation of gene therapy-based protein products. Duties include: Collaboration with Therapeutic Target Leads to identify required Bio-reagents. Collaboration with Molecular Biology Core and Protein Expression Analysis teams for required DNA constructs. Expression and purification of bio-reagents. Screening of commercial antibodies against targets of interest. etc./ | 4/29/2019 |
| 15492 | Amneal Piscataway, NJ Safety Engineer BS/BA in environmental health/safety Exp: 1+ year in health/safety |
The Safety Engineer works with the Supervisor to plan, direct and implement Amneal's environmental health and safety programs to ensure a positive, safe, healthy and incident-free work environment and is responsible for the compliance by Amneal with all environmental and safety regulatory agencies. Responsibilities include: Walk each plant periodically to observe operations and identify safety issues, assess and correct any problems. Ensure fire extinguishers are in working order, not blocked, conduct annual inspections with outside contractor, and verify that they are properly placed and hung. For NJ position: Weekly inspections of Laboratory and hazardous waste area required. Obtains OEL, SDS and SFS for all products with a focus on NPL and R&D projects. Ensures that proper information is communicated to user department and training is provided, as required. | 4/29/2019 |
| 15493 | Amneal Brookhaven, NY QA Inspector I HS Diploma/GED Exp: 1+ years in QA |
To monitor and ensure all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. To monitor and ensure all phases of drug manufacturing are in compliance with established specifications. To receive, inspect, release and control of labels and outserts. To ensure quality compliance before, during and after each packaging run. Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. Preparation of samples for chemical and microbiological (where required) analysis and delivering them to the QC lab. Inspection and test of packaging components utilizing various measuring devices such as scales, micrometers and height gauges to determine conformance to specifications. Maintaining detailed records of sampling, inspections and testing activities. Assigning and verification of expiry date and retest date for all the GMP raw materials through vendor COA and in-house COA. Collection of packaged product samples for annual stability. | 4/29/2019 |
| 15494 | Amneal Brookhaven, NY QA Inspector I HS Diploma/GED Exp: 1+ years in QA |
To monitor and ensure all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. To monitor and ensure all phases of drug manufacturing are in compliance with established specifications. To receive, inspect, release and control of labels and outserts. To ensure quality compliance before, during and after each packaging run. Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. Preparation of samples for chemical and microbiological (where required) analysis and delivering them to the QC lab. Inspection and test of packaging components utilizing various measuring devices such as scales, micrometers and height gauges to determine conformance to specifications. Maintaining detailed records of sampling, inspections and testing activities. Assigning and verification of expiry date and retest date for all the GMP raw materials through vendor COA and in-house COA. Collection of packaged product samples for annual stability. | 4/29/2019 |
| 15495 | Amneal Bridgewater, NJ IT Support Associate HS Diploma/GED Exp: 1+ years |
The IT Support Associate will support team members by providing prompt response to members' problems and requests while managing and maintaining the closing of tickets within Servicedesk Plus ticketing system. As a team member, he/she will function as the primary interface for the Corporate IT Team providing a positive experience for Amneal's team members through tailored IT solutions. He/she will be responsible for team members' computer and account management provisioning and de-provisioning as well as inventory management of equipment. Installation, configuration, and support of network resources including printers, VOIP phone system and other peripheral devices among many other tasks will be a part of daily duties. IT Support Associate will work on all aspects of problem resolution for team members; this includes but is not limited to driving the resolution from IT Support teams, cross-functional organizations, and external vendors. Using your expertise, you will identify opportunities for continuous process improvements and if needed, partner with other Amneal technology teams to design, plan and implement a resolution. | 4/29/2019 |
| 15496 | AMPAC Rancho Cordova, CA Quality Assurance Analyst BS/BA in sciences Exp: 1-5 years |
Duties may include: Review and/or conduct investigations for process variances, product non-conformances OOS results. Ensure compliance of current processes and planned process improvements to cGMP. Be responsible for the timely review of records, to include confirming the completeness of the record and the accuracy of relevant entries. Manage the release of intermediates and final products in accordance with the approved systems, procedures and specifications.. | 4/29/2019 |
| 15497 | Amphastar Pharmaceuticals Inc El Monte, CA Validation Technician BS/BA Exp: 0-2 years |
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties maybe assigned. Coordinates and performs validations on equipment and process such as autoclaves, ovens,aseptic processes, product assembly lines, filling machines, sterilization processes, and cleaning process. Performs basic validation techniques and activities to report on product,equipment, and process performance to assure Company's standards are met. Works with Operations to assure work is completed without manufacturing interruption | 4/29/2019 |
| 15498 | Amphastar Pharmaceuticals Inc Inland Empire, CA Microbiologist BS/BA in biological sciences Exp: 1-2 years |
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Performs test preparation and setup, and runs required tests for pharmaceutical raw material and finished products, such as bioburden, sterility and endotoxin tests. Performs a variety of tests which directly or indirectly affect product release, and test for the sterile quality of products manufactured by performing the following duties. Analyzes test data collected from experiments using laboratory equipment and chemicals to determine the sterile quality of products produced. Interpret EM plates and RCS strips. Identify isolates recovered from EM plates/strips and bioburden tests. Writes test results and submits reports including required calculations and statistical verifications. | 4/29/2019 |
| 15499 | International Medication Systems South El Monte, CA Operations Assistant - Engineer BS/BA in chemistry, biochemistry, or engineering Exp: 0-2 years |
Plans and coordinates activities of pharmaceutical production processes, process improvement and development, equipment renovation, quality assurance/quality control, training, and other duties by performing the following tasks personally. Coordinates and conducts daily operational activities and provides support to all departments. Plans, coordinates, and directs programs for pharmaceutical, medical product order fulfillment, product development, improvement of manufacturing processes; or for analysis and testing of substances to support quality control efforts. Generates and revises standard operation procedures. Reviews protocols from Validation and Quality Control Laboratory and engineering reports. | 4/29/2019 |
| 15500 | AMRI Grafton, WI QUALITY ASSURANCE ASSOCIATE BS in chemistry or related Exp: 1-3 years |
The Quality Assurance Associate is an integral part of the AMRI team, contributing to our success by assuring that all documentation, procedures and protocols comply with GMP and FDA guidelines. In this role you will: Conduct batch record and test data reviews, and approve batches for release. Assist in maintaining compliance of Environmental Monitoring, Equipment Calibration, and the Equipment Maintenance Program. Issue Deviation, CAPA, and OOS investigations. Track investigations and outcome. Review and recommend approval of indicated actions to senior associates or quality management. | 4/29/2019 |
| 15501 | AMRI Alburquerque, NM Microbiologist I BS in life sciences Exp: 0-2 years lab experience |
Prepare, collect, and test plant purified water, manufacturing raw materials, product in-process, and finished product, and perform environmental monitoring. With limited supervision, learn and perform critical laboratory techniques and complete original work. Author problem reports and participate in investigations. This description is inclusive of EM and testing duties: actual percentages of time spent on each duty may vary based on business needs. | 4/29/2019 |
| 15502 | AMRI Burlington, MA Microbiologist BS/BA in sciences, microbiology preferred Exp: 1+ years in GMP/GLP environment |
The Quality Control Microbiologist performs quality activities in support of product production and releases. The QC Microbiologist performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. This includes: Perform microbiological testing (endotoxin, bioburden) for water. Perform microbiological testing (endotoxin, sterility and bioburden) for raw materials, in-process materials, intermediates and final product. Read, trend and report environmental, personnel, in-process, raw material, finish product and water bioburden testing results. Maintain historical files on organisms found in classified areas; microbial identification and trending. etc. | 4/29/2019 |
| 15503 | Analogic Peabody, MA Associate Mechanical Engineer BS in mechanical engineering or related Exp: 0-3 years |
Performs mechanical design tasks on subunits of larger projects. Requires knowledge of engineering principles and concepts, an ability to understand the integration of designs and subunits within the overall project, and consistent application of acquired knowledge. Designs, modifies and evaluates mechanical and electro-mechanical apparatus components and processes. Applies original and creative approaches to design tasks. Plans and conducts engineering research, design, development or manufacturing engineering assignments. Estimates engineering personnel requirements. Schedules work to meet completion dates and technical specifications. Makes changes in methods, design or equipment where necessary. Generally operates with appreciable latitude for unreviewed action or decision. | 4/29/2019 |
| 15504 | ARL BioPharma Oklahoma City, OK Laboratory Technician - Microbiology Lab AS or BS/BA in microbiology or related Exp: 0-2 years |
Under the supervision of the laboratory supervisor the Microbiology Lab Technician provides support tasks in a fast-paced laboratory setting. Funtions include: Media preparation, Glassware cleaning, Inventory / ordering, Lab cleaning and sanitization, Autoclaving various reagents and supplies, Assist laboratory personnel in daily activities to maintain high scientific quality and compliance with SOPs, protocols, and safety standards | 4/29/2019 |
| 15505 | ANI Pharmaceuticals Baudette , MN Operator I - Manufacturing and Packaging (1st and 2nd Shift) HS Diploma/GED Exp: 1-2 years |
Position Responsibilities: Assists in material handling, equipment set-up and breakdowns, documents process according to Master Production Records, and works with trained operators at assigned work centers to learn all aspects of the position, including batch record documentation, equipment set-up, operation and clean up. | 4/29/2019 |
| 15506 | ANI Pharmaceuticals Baudette , MN Contracts Support Associate AS Exp: 1-2 years |
This position is responsible for daily data entry as it relates to Contract Support related activities. This includes order processing, shipping paperwork, invoicing, advanced ship notices, product returns and other duties as assigned. Position Responsibilities: This includes: 1. Order Entry – Receipt/entry (EDI, Fax, e-mail). 2. Shipping/Invoicing – Prepare all docs pre and post shipment, maintain files, send invoices and advanced ship 3. CSII Orders – Process, verify, track orders, and maintain electronic 222 log. 4. Receive and update returns log for all return requests received by customers. 5. Evaluate each return to determine the appropriate return policy. 6. Create Disposition Authorization. 7. Coordinate with return company and/or customer on return or destruction authorization. 8. Create credit request for approval once material returned or destruction notice received. 9. Enter approved credits/debits into customer accounts. 10. Provide customer with credit and any supporting documentation. 11. Performs other duties as assigned or requested. | 4/29/2019 |
| 15507 | Antech Diagnostics Columbia, OH Laboratory Generalist AS/BS in sciences or veterinary technician Exp: 1+ years lab experience |
You will be using automated analyzers, microscopes and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries and diseases in support of veterinarian animal treatment. You will be responsible for setting up and running lab tests, and reading and releasing results according to SOPs (Standard Operating Procedures). You can expect to specialize in one or more of the following areas: Hematology, Urinalysis, and Chemistry/endocrinology. | 4/29/2019 |
| 15508 | Antech Diagnostics Mississaugua, CA Specimen Processor HS Diploma/GED Exp: 1+ years lab experience |
The Specimen Processor receives and prepares samples for laboratory analyses and tests. Prepares samples on slides or other testing format, records required information and sends to appropriate specialty lab area. Receives and prepares samples for laboratory analyses and tests to diagnose various pet and other animal illnesses, injuries and diseases in support of veterinarian animal treatment. Records information about specimens. Labels and numbers slides, specimens and submittals. Enters specimen data into tracking system. Make copies of submittals. Matches test slips with incoming specimens. Prepares work lists for each testing department. Verifies accuracy of information. | 4/29/2019 |
| 15509 | Antech Diagnostics Fountain Valley, CA Laboratory Aid HS Diploma/GED Exp: 1+ years lab experience |
Antech Diagnostics is looking for outstanding Laboratory Aides and Assistants for Overnight Shift positions throughout our veterinary diagnostic reference lab locations. The ideal candidates will have experience working in either a reference or hospital laboratory, or have strong experience performing lab duties as a Vet Tech. The Laboratory Aide is responsible for setting up instruments, collection of samples, load samples into instruments and prepare samples for laboratory technicians. | 4/29/2019 |
| 15510 | Antech Diagnostics Irving, TX Laboratory Aid HS Diploma/GED Exp: 1+ years lab experience |
Antech Diagnostics is looking for outstanding Laboratory Aides and Assistants for Overnight Shift positions throughout our veterinary diagnostic reference lab locations. The ideal candidates will have experience working in either a reference or hospital laboratory, or have strong experience performing lab duties as a Vet Tech. The Laboratory Aide is responsible for setting up instruments, collection of samples, load samples into instruments and prepare samples for laboratory technicians. | 4/29/2019 |
| 15511 | Applied Medical Rancho Santa Margarita, CA Product Quality Engineer BS/BA in mechanical, biomedical, or electrical engineering Exp: 1+ years in med device industry |
As a Product Quality Engineer, you will be responsible for working within the framework of a team and performing the following activities: Evaluate the performance of products returned by the customer. Perform device analysis in accordance with model-specific procedures and protocols. Perform root cause analysis to investigate alleged product deficiencies. Propose corrective/preventive actions as required. Compose detailed reports describing results from investigations. | 4/29/2019 |
| 15512 | Applied Medical Rancho Santa Margarita, CA Process Engineer I BS in mechanical, biomedical, industrial, or manufacturing engineering Exp: 0-2 years in engineering |
As a Process Engineer I, you will learn and develop skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. Responsibilities include: Sustain manufacturing processes. Debug manufacturing processes and equipment via root cause analysis. Develop and update engineering documents such as process maps, process FMEA, manufacturing/quality Instructions, test methods, drawings, and test reports. Collaborate with the Engineering team for fixturing design and development, tolerancing and design for manufacturing | 4/29/2019 |
| 15513 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I BS in engineering or STEM Exp: 0-2 years in engineering |
As a Quality Engineer I, you will learn and develop skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. Responsibilities include: Conduct experiments to prove hypotheses. Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques. Implement statistical techniques to determine sample sizes and levels of confidence. Design engineering test protocols and use a data-driven approach to collect, analyze and summarize data into engineering reports | 4/29/2019 |
| 15514 | Akoya Menlo Park, CA Associate Scientist, Reagent Development MS Exp: 0-2 years in histology/microscopy |
You will beresponsible for developing applications and products for Opal Multiplex Fluorescent IHC Reagents which are designed specifically for Akoya’s cutting-edge Mantra and Vectra Polaris multispectral imaging systems.The desired skillset for laboratory work includes the ability to perform immunohistochemistry (IHC) procedures to support theproductdevelopment. Your work will involve manual laboratory work and the use of automated stainersystems for monoplex and multiplex fluorescence tissue staining. | 4/26/2019 |
| 15515 | Akrevia Therapeutics Cambridge, MA Sr. Research Associate, Immuno-Oncology(FACS) MS Exp: 1+ years in biotech/pharma |
We are seeking a Senior Research Associate to join our Immunology group. This person will be responsible for developing, qualifying, and performing assays to assess immune function in support of Immuno-Oncology programs. Responsibilities include: Support the characterization of the immune state of ex vivo and in vivo tumor models through a variety of means including FACS analysis. Develop assays to assess immune function including T-cell, NK cell, macrophage function in a variety of formats. Integrate technologies that improve or expand the ability to assay molecules by working with teammates, collaborators, vendors, and staying abreast of the literature | 4/26/2019 |
| 15516 | Alan Laboratories San Diego, CA Chemistry Lab Technician BS in chemistry or chemical engineering Exp: 0-2 years |
To conduct formulation preparation or analytical test in direct support of the drug development team, including writing documents and reports. Responsible for the maintenance of lab instrumentation and general lab duties. Prepare drug formulations according to established procedures. Analyze test data, recognize results that are abnormal or deviate from those expected. Recognize equipment malfunction and factors affecting measurements and testing. Evaluate and solve problems related to sample preparation, variation and processing | 4/26/2019 |
| 15517 | Alcami Germantown, WI Process Chemist (Night shift) BS in chemistry or sciences Exp: 0-4 years |
The Process Chemist I is accountable for driving results in a fast-paced environment by understanding reaction mechanisms and applying them to practical execution of given synthesis. Optimization of conditions to proposed and designed synthetic routes including but not limited to purity, loadings, equivalents, cycle times, work up procedures, and yields. The Process Chemist I must understand and able to perform routine analytical procedures to monitor reaction progress (i.e. TLC, GC, NMR, HPLC, KF) and be able to isolate and purify products and intermediates by using standard laboratory techniques . The Process Chemist I must document using GMP Good Documentation Practices and prepare final reports for completed projects, including final procedures and compiling all analytical data. | 4/26/2019 |
| 15518 | Alcami Germantown, WI Chemical R&D Associate Scientist II MS in chemistry or related Exp: 0-2 years |
The Associate Scientist II, under the direction of a senior scientist, executes chemical reactions on a gram to multi-kilogram scale and performs routine analytical procedures to monitor reaction progress. This role requires the incumbent to efficiently organize routine work with supervision and properly evaluate and interpret generated data. Exercises judgment within defined procedures and practices to determine appropriate action. The Associate Scientist II will exercise judgment within defined procedures and practices to determine appropriate action | 4/26/2019 |
| 15519 | Alcami Wilmington, NC Associate Scienstist, Biotech MS in pharma sciences, chemistry, or related Exp: 0 years |
The Associate Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also be required to work on method development/method validation projects. For this position HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) | 4/26/2019 |
| 15520 | Alcami Durham, NC Associate Scientist MS in pharma sciences, chemistry, or related Exp: 0 years |
The Associate Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also be required to work on method development/method validation projects. For this position HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). | 4/26/2019 |
| 15521 | Alcami Wilmington, NC Associate Scientist MS in pharma sciences, chemistry, or related Exp: 0 years |
The Associate Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also be required to work on method development/method validation projects. For this psotion HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). | 4/26/2019 |
| 15522 | Alcami Germantown, WI Analytical Chemist I BS in chemistry or related Exp: 0-2 years in API GMP manufacturing |
The Analytical Chemist I is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. This position may also be required to work on method development/method validation projects. Typical types of testing include: assays (potencies, related substances, residual solvents, metals etc.), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, DSC, TGA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by Alcami). | 4/26/2019 |
| 15523 | Aldevron Fargo, ND Quality Control Analyst I - Research Grade Manufacturing BS in sciences Exp: 1+ years in lab |
Our Quality Control Analysts are responsible for performing testing and sampling of our products in a laboratory environment. Responsibilities include; Perform all established assays as well as routine and non-routine laboratory testing. Act as primary analyst for production projects and complete appropriate documentation. Perform testing and sampling to support manufacturing, validation, and process development | 4/26/2019 |
| 15524 | Abbott San Diego, CA Production Chemist I BS/BA in chemistry or biological sciences Exp: 0-2 years |
Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. Responsibilities include: Carry out production tasks in support of manufacturing goals and objectives. Operate laboratory equipment safely, as trained and directed, in accordance with established practices. Maintain records and notebooks as directed in a neat, thorough and accurate manner. Perform required data entry on company planning and materials management system. Report results to supervisor. Perform complex formulations, component and material evaluations, equipment calibrations and maintenance | 4/26/2019 |
| 15525 | Abbott San Diego, CA Process Engineer I BS in engineering Exp: 0-2 years |
In this role, you will provide technical expertise and tactical coordination for successful implementation of components, processes and equipment for product development and/or production. Responsibilities include: Design and implementation of manufacturing processes from the laboratory and concept stage through pilot plant and manufacturing scale-up. Responsible for identifying and implementing improvements to both day to day operations and high-level systematic changes associated with ensuring all processes and functions come together to achieve throughput and quality goals. Interfaces with various departments to ensure processes and designs are compatible for new product technology transfer and to establish future process and equipment automation technology. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Acts as advisor and/or supervises subordinates in solving technical problems. Frequently interacts with departments, peers management and scientists. | 4/26/2019 |
| 15526 | Abbott Scarborough, ME Production Specialist I Nights HS Diploma/GED Exp: 0-2 years |
The position of Production Specialist I is within our Infectious Disease Developed Markets business unit located at Scarborough, Maine. In this role you will perform work required for the assembly of components, devices, and/or the final product depending on the trade assigned. Duties include: Performs work required for the assembly of components, devices and/or the final product with supervision. Ensures quality of product using standard operating procedures, templates, training and supervision, and good judgment. | 4/26/2019 |
| 15527 | Alexza Mountain View, CA Quality Control Analyst I BS in sciences or related Exp: 0-2 years in cGMP QC environment |
Responsibilities include: Provide timely analyses to support manufacturing and stability. This includes routine analysis of raw materials, in process and release of commercial product or clinical supplies. Under general guidance, perform assays under GMP, maintaining data integrity and ensuring compliance with company SOPs and specifications . | 4/26/2019 |
| 15528 | Alexza Mountain View, CA Research Associate I BS or MS in chemistry or chemical/bio engineering Exp: 0-2 years research experience |
Responsibilities include: Conduct research on various drug/device interactions as part of the drug delivery and device development process. Analyze and interpret data from various product development experiments. Exercise technical discretion in the design, execution and interpretation of experiments that contribute to project objectives. Contribute to stability studies. Ensure reproducible and reliable results for protocols related to development of drug delivery systems. | 4/26/2019 |
| 15529 | Align San Jose, CA Regulatory Affairs Specialist BS in engineering or sciences Exp: 0-2 years |
The primary responsibilities of this position will be premarket regulatory activities to support U.S. and international filings. Responsibilities include creating regulatory strategy for new products, supporting submission related activities, and interfacing with outside regulatory agencies. This position reports to the Director of Quality Assurance and Regulatory Affairs. Support assigned U.S. and international product/software registration activities; including assisting with the development of the regulatory strategy, 510k and international filing determinations, Technical Files, and international product registrations. Compile information from multiple sources for submissions, providing support to the project teams in creating documentation for submissions and assuring compliance with Design Control and Software Life Cycle SOPs. | 4/26/2019 |
| 15530 | Alkahest Inc San Carlos, CA Research Assistant/ Research Associate (in vivo) - Wednesdays thru Sundays BS/BA in life/biomedical sciences Exp: 1+ years |
The role will use in vivostudies to primarily assess CNS mechanisms through rodent behavioral, histological and biochemical techniques. The role is critical in assisting the scientific team in advancing our therapeutic understandings. This person will be involved in establishing, validating, and implementing methodologies in Alkahest’s laboratories and is thus pivotal to the company’s mission. The studies performed will involve cutting edge science and require innovative concepts and strategies. The role requires dedication to drive science, flexibility, excellent communication and organization, and will interact with a team of scientists and research associates to drive multiple projects in parallel. | 4/26/2019 |
| 15531 | Alkermes Waltham, MA Engineering Coordinator AS or BS/BA in relevant field Exp: 0-2 years |
The Alkermes Site Operations department has an opportunity for a full-time Engineering Coordinator. This position will coordinate service and project-related activities for the Site Operations department while providing technical and administrative assistance to other Site Operations team members as directed. Responsibilities include: Serve as the administrative contact / liaison with internal departments and external parties in order to develop engineering requirements and manage resource availability. Develop written documentation and correspondence for the department; screen and evaluate incoming and outgoing responses as appropriate. Gather, enter, and/or update data to maintain departmental and equipment records / databases, as appropriate. Establishes and maintains files and records for the department. Responsibilities include administration of the Maximo (CMMS/EAM) system including managing work schedules / work orders as well as keeping the system up-to-date. Ensure high Good Manufacturing Practices (GMP) and Environmental Health and Safety (EHS) standards are maintained, while adhering to schedules to meet the business requirements. Assist as needed in regulatory agency inspections. | 4/26/2019 |
| 15532 | Allergan Branchburg, NJ Associate Regulatory Compliance Analyst BS/BA Exp: 0-2 years |
Under the supervision of Regulatory Compliance management, the Regulatory Compliance Auditor/Analyst will support all aspects of the Regulatory Compliance processes which include but not limited to the activities listed below. Complies with FDA, ISO, AATB, and all other applicable international and state regulatory requirements, best industry practices and internal processes. Compile Quality metrics for QSMR, Tier board etc. and identify and bring issues to management when a compliance gap or quality issue is identified. Supports LifeCell’s internal audit program and performs assigned internal audits under the guidance of lead auditor in accordance with internal procedures and relevant standards/regulations. | 4/26/2019 |
| 15533 | Allergan Branchburg, NJ Associate Supplier Quality Engineer I BS/BA Exp: 0-2 years |
Under the supervision of supplier quality management, the Supplier Quality Engineer I will support all aspects of the Supplier Quality processes which include but not limited to the items listed below. Complies with FDA, ISO, AATB, and all other applicable international and state regulatory requirements, best industry practices and internal processes. Identify and bring issues to management when a compliance gap is identified. | 4/26/2019 |
| 15534 | Allergan Irvine, CA Laboratory Ops Associate AS or BS/BA in life sciences or chemistry Exp: 0-2 years lab experience |
The Lab Ops Associate is based in Irvine, CA and will support Allergan R&D by ensuring optimal operation efficiency of the laboratories. Primary area supported is Research and External Scientific Innovation, and includes multi-disciplinary interaction with EH&S, Managed Lab Services, Facilities & Corporate Engineering, and Pharmaceutical Development with emphasis on planning, coordinating and executing logistical lab operations. Responsibilities include: Scheduling technician visits and escorting the technicians into restricted lab spaces. Tracking research lab equipment including inactive, new, movement, and repair or calibration schedules. | 4/26/2019 |
| 15535 | Alliance Spine San Antonio , TX Full-Time Inventor Expeditor HS Diploma/GED Exp: 1+ years warehouse/inventory operation |
The inventory expeditor will work with other members of the inventory team to increase company profitability and customer satisfaction by delivering complete, accurate and on-time deliveries to the company’s customers. Responsibilities include: Deliver orders/inventory via the most effective route to ensure devices/products are delivered according to established time frames. Maintain communication with the Inventory Manager during deliveries to ensure any updated instructions are received. Operates a motor vehicle according to applicable state laws as needed. | 4/26/2019 |
| 15536 | Alnylam Cambridge, MA Associate Scientist: RNA Synthesis BS or MS in chemistry, biochem, or related Exp: 0-4 years |
The successful candidate will help to synthesize and purify oligonucleotides for research studies. Additionally, they will evaluate new chemical modifications for their use in the RNAi pathway via synthesis, purification, and characterization of synthetic oligonucleotides. Other responsibilities include: Utilize analytical instrumentation such as UV-Vis spectroscopy, HPLC, and/or LC-MS for the analysis of both crude and purified synthetic products. Effectively troubleshoot synthetic/process issues and independently find solutions. Improve upon and/or develop new methods and automation for the downstream processing of synthetic oligonucleotides and their subsequent analysis/purification and annealing into siRNA duplexes. | 4/26/2019 |
| 15537 | Agtc Alachua, FL Engineer I/II Upstream Process Development MS in bio/chemical engineering or realted Exp: 0-2 years |
The Engineer I/II in Upstream, Process Development will report directly to the Associate Director, Upstream Process Development at the Alachua, FL headquarters. Duties and responsibilities include: Plan, execute, and troubleshoot experiments for the optimization of upstream process steps in flasks and bioreactors for approved research plans. Optimize process parameters to increase virus yield from adherent & suspension cell lines. Responsible for scale up and manufacturing of viral vectors up to 200 L in bioreactor. Collect, analyze, record, and summarize data in the course of biologics production and processing Assist in maintaining laboratory supplies and equipment. | 4/22/2019 |
| 15538 | Agtc Alachua, FL Research Associate II/III/IV – Target Validation MS in biology or life sciences Exp: 0-2 years lab experience |
AGTC is seeking a highly motivated individual to support our drug development activities. They will be responsible for discovery research, implementing a scientific plan, and working independently in the lab with minimal supervision. Duties include: Target validation of candidate capsids, promoters, gene constructs, etc. Develop and qualify new assay methods. Execute routine assays and procedures. Collect, analyze, record, and summarize data. etc | 4/22/2019 |
| 15539 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Assistant – Formulations BS in life sciences Exp: 0-2 years |
The Drug Product Formulations Manufacturing Assistant is responsible for execution of routine production and manufacturing procedures to support processes and ensure compliance with regulatory requirements. The Manufacturing Assistant will work with the Drug Product team to ensure the successful completion of various cGMP activities. The Manufacturing Assistant will learn and demonstrate proficiency in both the technical aspects as well as the quality systems which govern cGMP manufacturing. | 4/22/2019 |
| 15540 | Ajinomoto Bio-Pharma Services San Diego, CA Document Control Assistant HS Diploma Exp: 0-2 years in GMP environment |
Ajinomoto Bio-Pharma Services is currently seeking a Document Control Assistant responsible for coordinating the review and approval of GMP documents using an electronic document management system. Responsibilities include: Coordinates document changes within an electronic document management system. Issues batch records, laboratory notebooks, and logbooks for use in GMP production and testing activities. Interfaces with document authors and reviewers to process document changes within project timelines and in accordance with established procedures. Ensures proper maintenance of document master copies and original production records. | 4/22/2019 |
| 15541 | Ajinomoto Bio-Pharma Services San Diego, CA Clean Room Monitoring Assistant - Multiple Openings HS Diploma or BS in life sciences Exp: 0-2 years |
This role is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As a Clean Room Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. Performs environmental monitoring within the microbiology laboratory, manufacturing suites, clean rooms, and drug product operations. Performs enumeration and gram staining of bacterial colonies. Maintains lab area including routine cleaning of benches, biosafety cabinets, shelving and floors | 4/22/2019 |
| 15542 | Akorn Decatur , IL Quality Assurance Technician HS Diploma Exp: 1+ years |
The QA Auditor I performs quality assurance duties at the assigned facility to prevent or eliminate defects in products for sterile filling operation or in final inspection and packaging operations. This individual must work in a detail-oriented, compliant manner in a high stress environment where adherence to deadlines is critical. The individual must display exemplary level of integrity at all times. The QA Auditor reports directly to the QA Supervisor or Manager of Quality Operations. Duties include: Check the production lines to make sure the right product is issued to match batch record. Monitor the production processes and ensure consistency of procedures. • Review/approve raw materials or components for use in production, etc. | 4/22/2019 |
| 15543 | Akorn Decatur , IL 2nd shift Formulation Technician I HS Diploma Exp: 0-2 years |
Formulation Technician I will be responsible for performing formulation of pharmaceutical and ophthalmic product solutions for lyophilized products. Assures proper documenting procedures and transfer of solutions to appropriate areas. Supports the development of products or processes, quality control, and proper maintenance of environmental standards. Duties include: Formulation of product solutions as well as cleaning/sanitizing solutions. Set up / Post use cleaning of formulation equipment. Transfer of product and non-product related solutions to filling areas. Following Standard Operating Procedures and Batch Record processes. Assuring proper documentation of all duties performed and material usages. | 4/22/2019 |
| 15544 | Akorn Decatur , IL Microbiologist I - NJ - 2nd shift BS or MS in biology or life sciences Exp: BS: 1-2 years, MS: 0 years |
Hours are from 3PM-11:30PM. Under limited supervision and guidance of the Microbiology management team, the Microbiologist I is responsible for the following duties: Performs routine microbiological testing of products, raw materials, components and controlled environments according to site Standard Operating Procedures and compendial methods. Documents routine procedures following laboratory and company guidelines. Issues and revises GMP documents such as SOP’s, protocols/reports, testing monographs, data sheets, etc. | 4/22/2019 |
| 15545 | Abcam Burlingame, CA Research Associate, IVD BS in biochemistry, pathology, or life sciences Exp: 1+ years lab experience |
This position will contribute to the development and validation of qualified reagents and generate data to support IVD products. Protocols and associated data may include immunohistochemistry (IHC), western blots, ELISA or other immunoassays, immunofluorescence or others as required. In addition, this position will be expected to complete scientific and technical tasks on aggressive timelines and to work as part of a team on varied tasks with changing priorities. | 4/21/2019 |
| 15546 | Abcam Burlingame, CA Project Coordinator (Custom Antibody Development) BS in biology or other life sciences Exp: 1+ years |
The project coordinator will join a dynamic team within a rapidly growing organization and will be responsible for supporting custom antibody development projects, driving them toward major milestones and successful completion. This position will be an important addition to the US Custom Services team within our Burlingame office. The role will support project management functions including the sourcing of reagents, scheduling immunizations, supporting customer interactions, populating work reports and product datasheets. In addition, the appointed person will assist with the receipt and shipment of critical reagents and data entry. | 4/21/2019 |
| 15547 | Abpro Woburn, MA Research Associate, Antibody Engineering BS or MS in biology or life sciences Exp: 0-3 years |
We are seeking a motivated individual for a research associate/senior research associate position that will specialize in antibody/protein engineering, gene sequencing, mammalian cell culture, and antibody expression/purification. This person will have good opportunity to experience many different areas in therapeutic antibody discovery, molecular biology and cell biology as an integral part of our Antibody Discovery and Engineering team. Responsibilities include: Sequence antibody variable (VH/VL) regions. Construct and validate gene and plasmid constructs. Express antibody/protein genes in mammalian cell systems. Purification of antibodies/proteins | 4/21/2019 |
| 15548 | Absci Vancouver , WA Research Associate I BS in biology, biochemistry, or related Exp: 1-2 years lab experience |
The Research Associate I, under direction of the Molecular Sciences team, will support innovative experimental research that advances AbSci’s proprietary E. coli expression platform. Primary responsibilities include providing core support to ongoing DNA construction, strain engineering, and small-scale protein expression activities. Daily activities will include management of the Molecular Sciences laboratory consumables and sample libraries, preparation of common research reagents, and providing assistance to ongoing experiments. The ideal candidate will demonstrate rapid mastery of assigned tasks and the capacity to take on additional technical responsibilities within an expanding team. | 4/21/2019 |
| 15549 | Accuray Madison, WI Product Development Technician AS or BS in electrical technology or related Exp: 1+ years |
The Product Development Technician is responsible for assisting in various Product Development projects. Duties include: maintaining, modifying and repairing H-Series and Radixact Radiation Delivery Systems; maintaining and repairing test and lab equipment; performing tests, measurements, and analysis; assisting Engineers with various Product Development tasks; selecting and purchasing supplies, components, and assemblies for maintaining and testing. Duties include: Maintain, test, troubleshoot and repair radiation delivery systems and associated bunker support instrumentation, in accordance with quality system requirements and associated manufacturing and service procedures. Manage inventory of spare and alternate parts necessary to maintain and reconfigure radiation delivery systems; procure replacement/new parts through supply chain, manufacturing, and/or service as-needed. Obtain required data sets; assist in analyzing and presenting findings. | 4/21/2019 |
| 15550 | ACell Columbia, MD Materials Associate HS Diploma Exp: 0-3 years in manufacturing |
The Materials Associate I is primarily responsible for completing general warehouse functions. This includes, but is not limited to labeling and boxing product, verifying incoming product counts, conducting inventory counts, and reviewing documentation in order to maintain up-to-date inventory records. The Materials Associate I is also responsible for the packaging and shipping of finished devices to customers and sales representatives. | 4/21/2019 |
| 15551 | ACell Columbia, MD Biotechnician HS Diploma Exp: 0-3 years |
Employee will carry out manufacturing practices in a cGMP biotechnical facility. The job involves the manual processing of porcine urinary bladders, which includes all aspects from collection of raw materials to packaging of the final product. Following training, work will be expected to be performed independently to a high degree of standard in biomaterial handling. | 4/21/2019 |
| 15552 | Acutus Medical Carlsbad, CA Engineer I - Field Service BS in sciences/engineering Exp: 1+ years |
The Engineer 1 - Field Service is the responsible for providing highly visible onsite and remote technical support to customers of Acutus Medical. This includes but is not limited to installation, general servicing, repairing, problem solving and supporting customers and medical centers using the Acutus’ electromedical equipment. This Engineer works closely with Acutus’ internal teams to ensure customer feedback, experiences and input is communicated to the appropriate internal team members. | 4/21/2019 |
| 15553 | Emergent BioSolutions Lansing, MI Assistant Manufacturing Associate HS Diploma Exp: 0-1 years in cGMP environment |
Responsibilities as an assistant manufacturing associate include: Execute tasks per cGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing qualification block training program. Actively incorporate the Core Values set out by Emergent BioSolutions while performing day to day activities. | 4/21/2019 |
| 15554 | Emergent BioSolutions Baltimore, MD Associate Specialist Metrology Tech Sys BS in engineering or related Exp: 1-2 years |
The Associate Metrology Technical Systems Specialist is responsible the execution of the metrology functions required to support the facility and process equipment at the Baltimore fill/finish facility. Perform calibrations and schedule vendor calibrations of instrumentation and equipment. Repair and troubleshoot electronics and instrumentation as well as other equipment as able. Duties include: Designs, develops, implements and maintains calibration processes and procedures for new and existing equipment and instrumentation and train key personnel on proper use. Coordinates and performs calibration of instrumentation necessary for maintaining production equipment, laboratory equipment and other auxiliary measurement systems. Maintains detailed calibration record. | 4/21/2019 |
| 15555 | Emergent BioSolutions Baltimore, MD Analyst II, QC Microbiology MS in microbiology/biology Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Emergent BioSolutions Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. | 4/21/2019 |
| 15556 | Emergent BioSolutions Baltimore, MD Analyst I, QC Microbiology BS in microbiology/biology Exp: 0-2 years |
Analyst I of QC microbiology has responsibilities that include: Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. Perform various microbiological testing procedures as per manufacturing/Quality Control batch records, stability protocols, raw material requests for testing, etc. Perform environmental monitoring and utility testing of the facility. Performs environmental monitoring during fill operations. | 4/21/2019 |
| 15557 | Adaptive Biotechnologies Seattle, WA Research Associate I SB/BA in biology, chemistry, or related Exp: 1+ years lab experience |
The position will design and coordinate experiments which leverage Adaptive’s unique platform to realize the company’s strategic objectives in hematology, immunology and oncology. Responsibilities include: Develop new assays for immune system profiling by next generation sequencing in collaboration with a team of other researchers. Develop new methods and technologies for project advancement including novel molecular biology methods, streamlined protocols, and automating tasks. Transfer developed methods and/or assays into SOPs for the development laboratory and/or production laboratory . Responsible for analyzing data and reporting findings to their supervisor | 4/21/2019 |
| 15558 | Adaptive Biotechnologies Seattle, WA Quality Systems Associate I (GMP) BS or MA in sciences Exp: 1+ years in QA |
The Quality Systems Associate is responsible for supporting day-to-day operation and may have individual responsibility for working with new, or transferred, products to provide quality oversight to ensure regulatory compliance. The position is accountable for the applications of industry standard quality practices and tools as applied by Adaptive Biotechnologies. The position requires the ability to manage priorities from multiple projects and tasks utilizing effective written and oral communication skills. This position will apply quality systems knowledge, problem solving, and judgment skills to ensure the appropriate balance of quality, compliance, and business needs. | 4/21/2019 |
| 15559 | Adaptive Biotechnologies Seattle, WA Quality Systems Associate I BS in relevant sciences Exp: 1+ years in QC/manufacturing etc. |
This position is responsible for supporting the Quality Management System (QMS) by working with production staff to ensure compliance with regulatory and internal process requirements. The position is accountable for the applications of industry quality requirements, standards, and tools to continually improve the quality systems established at Adaptive Biotechnologies. The position requires the ability to manage priorities from multiple projects and tasks while utilizing effective written and oral communication skills. This position will develop quality systems knowledge, and apply that knowledge through reasoning and judgment, to ensure an appropriate balance of quality, compliance, and business needs. | 4/21/2019 |
| 15560 | Adimap Lebanon, NH Research Associate - Antibody Discovery BS or MS in biology, chemical engineering, biochemistry, or related Exp: 1+ years |
We are seeking a skilled molecular or protein biologist to join our Antibody Discovery team. The Research Associate will work in a small team setting to support Adimab’s novel antibody discovery, maturation, and production platform. This role will closely interface with the Protein Analytics, High Throughput Expression, Molecular Sciences, and Computational Biology teams. Duties include: yeast propagation, mammalian cell culture, antibody library construction/selection, etc. | 4/21/2019 |
| 15561 | ABL Inc. Rockville, MD Laboratory Research Specialist BS or MS in life sciences Exp: BS: 1-2 years, MS: 0-1 years |
This position will provide extensive technical support for fulfilling contract requirements for immunological assays. Duties include: Assist in the development and qualification of new immunological assays including; but not limited to, the following:Multicolor-Flow Cytometry based assays, cytokines and other soluble biomarkers Multiplexing assays (Luminex, Aushon, MSD platforms), ELISA, ELISpot, and Neutralization Assays, among others. Responsible for organizing and ensuring efficient daily operation of the laboratory including: stocking laboratory with necessary reagents and other materials used for experiments and inventory of reagents and samples. This position will ensure the accuracy of record keeping of experimental conditions and results. Assist withdaily scientific duties in the laboratory in order to meet commercial and government contract obligations in a timely manner. Lab activities mayinvolve interaction with other functions and departments. | 4/21/2019 |
| 15562 | Biotechne Wallingford, CT Reagent Manufacturing Technician AS or BS in biology, chemistry, or related Exp: 1+ years lab experience |
This position requires the ability to function with minimal oversight and convert customer demands into finished product. The individual will execute production protocols and ensure continual operation of equipment to meet production targets, effectively and immediately communicate complications that arise during manufacturing, and be able to work across teams to establish and maintain solutions. The individual must also demonstrate a proactive mindset to manage multiple tasks and drive them to completion in a timely manner. | 4/21/2019 |
| 15563 | Biotechne Minneapolis, MN Research Associate - New Technologies/Luminex MS in chemistry, biology or related Exp: 0-2 years |
The responsibilities of this position are to assist with validation, feasibility, product development, and technical support of immunoassays. Optimize components and performance, develop manufacturing procedures, transfer product/process to production, and perform necessary troubleshooting. Work on problems of moderate scope where analysis of situation or data requires a review of identifiable factors. Perform additional duties as assigned. | 4/21/2019 |
| 15564 | B. Braun Medical Inc. Allentown, PA Associate Engineer BS in engineering Exp: 0-1 years |
Provide Engineering support toward the design, development, installation, startup, validation, and maintenance of products, processes, and equipment. Provide engineering skills within a specialty field(s). Responsibilities include: Research, develop, and prepare specifications for improvements to existing and/or new products, processes, equipment, and technology. Support projects by contributing as a team member to the development of project schedules, costs, preparing status reports, attending team meetings, and communicating issues and progress to team and management. Assist in the supervision of contract personnel and outside vendors in the performance of contracted services. | 4/21/2019 |
| 15565 | B. Braun Medical Inc. Irvine, CA Product Handler HS Diploma Exp: 0 years |
Under the direction of the Supervisor/Line Operator/Process Monitor, monitors material in order to maintain efficient flow of production. Operate hand or power trucks and other material handling equipment. Responsibilities include: Operate hand or power trucks and other material handling equipment to move materials throughout the unit. Change batteries on these material handling equipment. Delivers first (1st) pallet and subsequent pallets to staging area after verifying correct quantity of empty trays. Load product onto pallets, trays, baskets or conveyors, checking product identification to verify correct lot number, description, etc. Discard, reject and record information as needed. Sign and date the back of each tag once the pallet has been verified as having the correct amount of units and trays. | 4/21/2019 |
| 15566 | B. Braun Medical Inc. Denver, CO IV Tech I HS Diploma Exp: 1+ years in aseptic prep |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Responsibilities include: Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. Participates in cleanroom product introduction activities. | 4/21/2019 |
| 15567 | Affigen Austin, TX Research Associate I/II MS in biology, chemistry, or related Exp: 1+ years in pharma/biotech |
Reporting to Senior R&D Scientists, the Research Associate will be a part of our growing lab group that is responsible for generating and characterizing test materials to support manufacture process development and preclinical studies required to rapidly advance Affigen’s patient-specific monoclonal antibody therapeutics into the clinical-phase. In this role, the Research Associate is expected to take ownership of specific processes, assays or instrumentation (listed below) and act as the in-house subject matter expert in these functional areas. In addition, the Research Associate will be required to perform miscellaneous laboratory duties that may broadly traverse aspects of upstream, downstream, and analytical development and general research support. A successful candidate for this position will be performance-focused, detail-oriented, and capable of filling a multidisciplinary supporting role across multiple research and development activities through excellent communication, documentation and teamwork skills. | 4/21/2019 |
| 15568 | AGC Biologics Seattle, WA Manufacturing Associate I-IV BS in chemistry, biology, or related Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Principle responsibilities include: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. | 4/21/2019 |
| 15569 | AGC Biologics Seattle, WA Contract Manufacturing Associate I-IV - Upstream BS in chemistry, biology, or related Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. | 4/21/2019 |
| 15570 | Agilent Wilmington, DE R&D Electrical Engineer BS or MS in electrical engineering Exp: 0 years |
As an Electrical Engineer in our R&D group, you'll be part of a team that analyze, design, prototype and test new products for Agilent's Gas Chromatograph, Automated Sample Handling and Automated Sample Preparation products. Electrical/Firmware Engineers at our site work on digital and analog PC board designs, algorithms for control of motion, flow and heated zones, intelligent systems. You will work with Real time systems, FPGA programming and robotic systems as well as thermal and pneumatic controls. One example would be a chemical sensor and circuitry to sense femtoamps of current. | 4/21/2019 |
| 15571 | Agilent Lexington, MA Inside Informatics Product Sales Specialist BS/MS in computer networking, chemistry, biology, or other sciences Exp: 0 years |
In this critical role, you will pair your experience with analytical instrumentation and our core markets, with your desire to sell, to drive growth in the Chromatography Data Systems, Data Management Systems, and Electronic Lab Notebook product lines. Responsibilities include: Act on sales leads for informatics systems, interpreting customer needs and developing solutions for these customers. Acquiring new customers and retaining and growing an existing installed base of customers.. | 4/21/2019 |
| 15572 | Agilent Wilmington, DE Analytical Instruments Technical Support BS in chemistry, biology, or related Exp: 0 years |
As an active team member, you will support customers requesting hardware, software and applications assistance with Analytical Products and Solutions and route those customers whom you can't help to the appropriate groups. Our group's organizational goal is that as part of a world-class technical support group, we provide insights to customers at their very first contact. In order to be successful, our response needs to be quick and well-informed. Direct customer contact through phone/email channels; Service Request logging in the Agilent SAP Service CRM system and request routing to the appropriate technical team for handling. | 4/21/2019 |
| 15573 | Agilent Washington DC, MD Field Service Engineer - Maryland/ Washington DC BS in chemistry, biology, or related Exp: 0 years (recent grads) |
As a field service engineer, you will work at a variety of labs, so having a solid understanding of Agilent's portfolio, and continuously learning about new instruments, software and consumables, is key. Applying your creativity, complex problem-solving skills, and can-do attitude is essential. Compliance and reporting are also important responsibilities, such as documenting and ordering components using a variety of databases. Having a natural instinct to deliver the highest-levels of customer service is vita | 4/21/2019 |
| 15574 | zPredicta San Jose, CA Research Associate, Cell Biology MS in life sciences Exp: 1+ years |
You will be responsible for executing projects for our pharmaceutical clients ranging from screening of investigational compounds to exploring the mechanism of action of drug candidates. Key responsibilities includes: Run customer projects under the guidelines and in collaboration with our pharma partners. Analyze data from multiple readout platforms including, but not limited to, flow cytometry, microscopy, viability and proliferation assays. Assist in adoption of zPREDICTA’s platform for high throughput use. | 4/19/2019 |
| 15575 | Zymergen San Francisco, CA Research Associate, Automation BS or MS in biology or life sciences Exp: 0-2 years lab experience |
The RA in this role will conduct experiments to test and validate new automation processes for high throughput engineering of microbial genomes. They will help to invent new techniques, create cutting edge protocols, and extend existing Zymergen protocols to provide newer and better workflows to our microbe engineering Factory. They will work together with other scientists, RAs, automation engineers, and software engineers to deploy these new technologies into production. The RA will contribute to the overall mission of Zymergen by helping to bring new technologies into our workflows. | 4/19/2019 |
| 15576 | Zymergen San Francisco, CA Research Associate I/II, Strain Banking BS/BA in biology, chemistry, engineering, or realted Exp: 0-2 years |
The Research associate will assist in supporting a number of cell banking activities, working with diverse microbes, following standard operating procedures (SOPs). The Biorepository team plays a key role in managing large collection of engineered microbes and DNA constructs which is key to enabling our engineering pipeline and the protection of Zymergen’s intellectual property. Key Responsibilities include: Executing day to day cell banking workflows for different projects, varying by type of host strains. Responsible for ownership of each project workflow, troubleshooting, as well as maintaining operational integrity . Adapting to complex multi-day experimental schedules and evolving standard operating procedures. | 4/19/2019 |
| 15577 | Zymergen San Francisco, CA Manufacturing Engineer, High Throughput Screening MS in life sciences Exp: 0-2 years |
Zymergen is hiring Engineers into the Manufacturing Engineering group to focus on the continual improvement of manufacturing workflows across our factory. These Engineers are required to be able to identify and implement improvements in existing processes and establish protocols for new programs. Typical responsibilities will include: Operation of multiple types of robotic systems, including but not limited to, liquid handlers, colony pickers, barcoders, and automated plate readers for implementation of new or improved processes. Process modeling using a bpmn based MES and workflow optimization in collaboration with software and automation teams. Development and implementation of data tools (JSL, Python, R, etc.) to support existing workflows. | 4/19/2019 |
| 15578 | Zymergen San Francisco, CA Research Associate I-III, DNA/Plasmid/Strain Production BS/BA in biology or related Exp: 1+ years in lab or manufacturing |
This Research Associates position will be responsible for either the DNA, Plasmid or Strain manufacturing processes within Production. The Research Associate will run a diversity automated workflows in a high-throughput environment. Key responsibilities include: Entering and processing data using custom software. Working with diverse integrated automation platforms to perform high-throughput cell and molecular biology workflows. Recognizing opportunities to improve workflows and communicating appropriately to manager and/or adjacent teams. | 4/19/2019 |
| 15579 | Zymergen San Francisco, CA Research Associate II/III, Genome Sequencing MS in biology, computer sciences, or related Exp: 1+ years professional experience |
This role is for an RA that will be an integral part of carrying out the sequencing core’s most essential function - sequencing. In particular this role is for an Reserach Associate that will be skilled at PacBio library preparation and instrument usage. Responsibilities will include preparing PacBio Sequencing libraries, writing SOPs for library preparation and instrument usage, work with Bioinformaticians and Software Engineers and IT staff to integrate PacBio sequencer into existing or new infrastructure and prepare sequencing libraries for other instruments. | 4/19/2019 |
| 15580 | Zymo Research Irvine, CA Research Associate MS in biology or rleated Exp: 0-2 years |
The incumbent will have demonstrated clear leadership potential with ability to efficiently multi-task and manage a scientific research project, starting from the initial idea through to completion and publication in a peer-reviewed journal. The successful candidate will also be a quick learner, have strong interest in science, and be passionate about a career in research. Responsibilities include: Assist in experimental design. Conduct complex, high-level scientific research activities. Optimize experimental procedures. Read scientific literature pertaining to project and apply relevant findings to research project. | 4/19/2019 |
| 15581 | 10xGenomics Pleasanton, CA Microfluidics Engineer BS or MS in engineering Exp: 0-2 years |
The candidate must be able to learn complex procedures, efficiently execute microfluidic characterization experiments, perform data analysis, and communicate results and observations effectively. Key responsibilities include: Perform experiments and analyze data to help us develop robust microfluidic consumables. Use your understanding of microscale transport phenomena and troubleshooting skills to engineer new products. Communicate results clearly and contribute data for making critical design decisions | 4/19/2019 |
| 15582 | 23andMe Mountain View, CA Software Engineer-Research Services BS/BA Exp: 1+ years |
Responsibilities include :Build web applications and APIs aimed at scientific researchers. Improve access to data and metadata throughout the company. Develop data visualizations. Secure customer data and protect customer privacy. Set up reliable, automated infrastructure in AWS. Deliver quality Python and Typescript code. | 4/19/2019 |
| 15583 | 23andMe Mountain View, CA Software Engineer - Machine Learning MS Exp: 1+ years |
Responsibilities include: Build applications, libraries, and services to make machine learning more available within the company. Expand the variety and complexity of machine learning modes we can use. Develop checks and tests to ensure we're delivering reliable, quality results. Optimize machine learning, computational, and data processing pipelines. | 4/19/2019 |
| 15584 | 3M Menomonie, WI UR – Corporate Engineering – Resident Project Engineer BS in engineering Exp: 0 years |
The successful candidate will have the opportunity to be involved with numerous 3M manufacturing processes, equipment and techniques, in numerous locations throughout the United States and the world. Responsibilities include: Manage project timelines and budgets for assigned projects. Successfully interact with multiple discipline teams including 3M plant personnel, consultants and suppliers. Specify equipment performance and design criteria. Estimate capital equipment and installation costs. Oversee plant equipment layout and design. | 4/19/2019 |
| 15585 | 3M Maplewood, MN UR - Cloud Analyst BS in engineering Exp: 0 years |
he person hired for the position of Cloud Analyst will work with the global process teams to build and deploy standardized global cloud solutions as part of the Polaris project. Responsibilities include: Design, develop and test data pipelines established to deliver data into data storage based on a function design specification. Analyze, design, code/develop and implement changes to resolve break/fix issues to resolve and close tickets during both testing cycle of project and in production. Understand the functionality of relevant process area and data that will be required to Build, Test and implementation. | 4/19/2019 |
| 15586 | 3T Biosciences Menlo Park, CA Computational Biologist BS/BA or MS in bioinformatics Exp: 1-2 years in bioinformatics or related |
We’re looking for enthusiastic and self-motivated individuals to bring their talents to a fast-paced environment. Responsibilities include: Processing next-generation sequencing data, such as RNA sequencing. Developing and applying algorithms such as clustering, principal component analysis and others to biological data such as gene expression information and immune repertoire data. Working with Amazon Web Services to process data. Working with a team of consultants, data scientists, and computational biologists | 4/19/2019 |
| 15587 | Abbott Abbott Park, IL Associate R&D Scientist, Diagnostics BS/MS in life sciences Exp: 0-2 years |
Main Responsibilities include: Experimental procedures: Conducts experiments, accomplishes established milestones and summarizes data. Recommends options for other experiments. Presents data within team. Expertise and Problem Solving: Troubleshoots instrumentation or experiments; recognizes and assists with technical problems. Project Planning: Participates in planning project tasks; providing input to accomplish assigned tasks. Lab Safety: Participates in routine maintenance and lab safety. Documentation: Appropriately documents experimental procedures and results according to established guidelines. Quality: Responsible for implementing and maintaining the effectiveness of the quality system. | 4/19/2019 |
| 15588 | Abbott Westford, MA Quality Engineer MS in related field Exp: 0-2 years |
Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. Core responsibilities include: Identifies and controls Manufacturing process defects (scrap, nonconforming material, custom complaints)by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying & bounding data to support implementation of complex & documenting release criteria.; Develops product quality plans, documents and systems by creating product specifications, quality specifications and quality plans in conjunction with other product development team members. May be responsible for creating risk analyses and FMEAs.; | 4/19/2019 |
| 15589 | Abbott Temecula, CA Quality Engineer MS in related field Exp: 0-2 years |
Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. Core responsibilities include: Identifies and controls Manufacturing process defects (scrap, nonconforming material, custom complaints)by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying & bounding data to support implementation of complex & documenting release criteria.; Develops product quality plans, documents and systems by creating product specifications, quality specifications and quality plans in conjunction with other product development team members. May be responsible for creating risk analyses and FMEAs.; | 4/19/2019 |
| 15590 | Abbott Santa Clara, CA R&D Engineer MS in related field Exp: 0-2 years |
Responsibilities as an R&D Engineer include: providing engineering support in the creation and development of new medical device products. Main responsibilities include: research, develop, and designs mechanica/electromechanical materials, components, assemblies, and processes. Conducts feasibility studies to verify capability and functionality. Developes new concepts from initial designs, etc. | 4/19/2019 |
| 15591 | Abbott Santa Clara, CA Associate R&D Engineer BS in related field Exp: 0-2 years |
Responsibilities as an R&D Engineer include: providing engineering support in the creation and development of new medical device products. Main responsibilities include: research, develop, and designs mechanica/electromechanical materials, components, assemblies, and processes. Conducts feasibility studies to verify capability and functionality. Developes new concepts from initial designs, etc. | 4/19/2019 |
| 15592 | Abbott Scottsdale, AZ Quality Engineer I BS in electrical engineering or technical field Exp: 0-2 years |
This position is responsible for supporting and improving quality engineering methodologies and providing quality engineering support within manufacturing, or system/services support. Responsibilities include: Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements. Assist in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements. Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues. Design and conduct experiments for process optimization and/or improvement. etc. | 4/19/2019 |
| 15593 | Abbott North Chicago, IL Quality Technician BS in sciences Exp: 0-2 years |
Candidate will undertake the role of technician quality with some supervision. Daily responsibilities include: CAPA -Provides inputs to facilitate CAPA investigations as required. Investigates standard complaints. Identifies and prioritizes medical and reportable complaints. Monitor performance of manufacturing processes and implement required improvement activities. Manage Product and Process Improvements - Participate in Project and Process improvement activities. Quality/Compliance -Support manufacturing and testing operations as required; adhering to Good Manufacturing Practices and Good Laboratory Practices. etc. | 4/19/2019 |
| 15594 | AbbVie Lake County, IL Associate Scientist I/II, Biotransformation DMPK BS or MS in chemistry Exp: BS: 1-4 years lab, MS: 0 years |
The candidate for this Associate Scientist I/II position will be working in the Biotransformation group of AbbVie’s Bioanalysis and Biotransformation department. This position will be focused on preparing biological samples and performing LCMS assays to characterize biotransformation of large molecules, including antibodies, antibody-drug conjugates, and proteins. The individual will be expected to have solid experience working with analytical instruments, especially HPLC and MS, and preferred to have experience working with protein samples and protein chemistry techniques. | 4/19/2019 |
| 15595 | AbbVie Lake County, IL Associate Scientist I, DMPK MS in life sciences Exp: 0 years |
The ideal candidate will have a strong background quantitative laboratory methods and mammalian cell culture. The position will require ability to generate precise, reliable and reproducible data in a timely manner. Demonstrate strong data interpretation skills, ability to troubleshoot experiments and instrumentation, ability to learn and understand new experimental techniques and be able to place data in proper scientific context by consulting and citing relevant literature. | 4/19/2019 |
| 15596 | AbbVie Worcester, MA Associate Scientist I/II, Modality Analytics BS or MS in chemistry Exp: BS: 1-4 years lab, MS: 0 years |
The candidate will be part of the New Modality Analytics Group within Protein Analytics that is mainly focused on method development and implementation of various HPLC, UPLC, and CE based analytical methods of AbbVie’s Biologics. The successful candidate will contribute to the development and testing of analytical assays and will contribute to the continuous improvement and innovation within the group and the PA department. | 4/19/2019 |
| 15597 | BioPharmGuy Anytown, US Contract Pipeline Research Assistant Some college Exp: 0 years |
We are looking for someone to confirm/correct our drug pipeline data on a contract basis. You should have some knowledge of drug indications and clinical phases of drug development. If interested, send us a message via our contact form. Must be able to accept payment via PayPal | 4/15/2019 |
| 15598 | Vyaire Medical Irvine, CA New College Graduate: Project Manager BS in engineering or project managemetn Exp: 0 years (new grad) |
The Project Manager function provides project support within a specialty R&D Engineering organization for new product implementation projects, improvement projects, and line extensions. The Project manager leads cross-functional team resources throughout the project life cycle and is accountable for meeting the agreed upon project scope, schedule, and budget within the directions of the Design Control Procedures. The Project Manager collaborates with internal cross functional resources and external partners (such as suppliers, vendors, testing labs and services) to properly staff their project and manage project risk. | 4/13/2019 |
| 15599 | Vyaire Medical Irvine, CA Graduate Program: Electrical Engineer BS/BA in electrical engineering Exp: 0-2 years |
We are looking for an Electrical Engineer Technician to join our Electrical Engineering team. In this role you will be responsible for sustaining activities of medical critical-care/home-care ventilator products. Duties include: Implement design updates for obsolescence of components, circuits, modules, power supplies, displays, etc. Perform root-cause analysis of production and field failures.. Ensure technical specifications meet product requirements as well as regulatory compliance and best design standards. Adhere to and improve documentation procedures in compliance with established Quality System and procedures and applicable domestic and international regulations. Perform design verification & validation. | 4/13/2019 |
| 15600 | Vyaire Medical Palm Springs, CA New College Graduate: Supply Chain - Operations BS/BA in engineering Exp: 0-2 years (new grad) |
The Graduate Program (GP) is intended to foster a pipeline of employees that deliver business critical results through outstanding performance, either as an individual contributor or as a future leader. As a member of the GP, you will have a unique opportunity to develop a broad knowledge base and skillset by working in one of the functional areas described below. GP participants will be paired with an mentor that will provide coaching and general guidance throughout the duration of the program, as well as a Functional Manager that will provide additional coaching, support and training. The functional manager will provide the goals and objectives for the position. The GP is intended to allow the graduate to learn the business and after 18 months within the program, potentially transition into another function and expand your career at Vyaire on candidate preference and organizational needs. | 4/13/2019 |
| 15601 | Vyaire Medical Irvine, CA New College Graduate: Complaint Analyst BS in engineering, chemistry, or life sciences Exp: 0-2 years (new grad) |
As a compliant analyst you will: Follow written procedures and standard work instructions to intake and process complaints. Collect basic information from customers and the knowledge gained from their specific customer experience. Forward information to appropriate internal parties as defined in written procedures, including complaint assessment based on formal flow charts, documentation and product knowledge. Prepare and submit USFDA’s MedWatch 3500A report, Health Canada’s MDPR, and/or EU’s MDV report as needed. etc. | 4/13/2019 |
| 15602 | TA Instruments New Castle, DE Manufacturing Engineer BS in mechanical engineering or related Exp: 1-3 years |
This person would be responsible for the manufacturing engineering activities of development and production programs through: the application of engineering procedures, which may involve theoretical and experimental investigation, technical direction and coordination, conception and planning of resources to support hardware requirement and; the analysis, evaluation and solution of technical problems encountered in the application of manufacturing methods, facilities, processes, materials and tooling incident to the fabrication and assembly of high technology instruments. | 4/13/2019 |
| 15603 | WAVE Life Sciences Lexington, MA Process Engineer I BS in chemical engineering Exp: 1-3 years in cGMP |
Working at the direction of the engineering leader, supports the implementation of production procedures to optimize manufacturing processes in a GMP environment. Assists with production process and/or scale-up. Assists manufacturing in problem solving with regards to equipment and systems. Collaborates with functions such as Process Development, Facilities, Quality, Supply Chain, etc. Oligonucleotide production process scale up by acting as a liaison between the Process Development and the Manufacturing teams. Support manufacturing operations and attend any equipment, process related technical issues. Troubleshoot production equipment and implement solutions. | 4/13/2019 |
| 15604 | Westat Rockville, MD Research Assistant BS in health or social sciences Exp: 1-3 years health related/research environment |
Westat is seeking a research assistant to provide patient registration support for a major National Cancer Institute contract. The primary function of this role is to set up and test patient enrollment forms in the patient registration system that enrolls patients onto oncology clinical trials. These services are provided Monday through Friday from 9:00 AM to 5:30 PM Eastern time. This position is located in our Rockville, MD office. Duties include: Setting up and testing patient enrollment forms in the patient registration system. Writing and testing logic checks. · Collaborate with the organizations leading the protocol to ensure accurate and timely availability of the forms in the system. | 4/13/2019 |
| 15605 | West-Ward Pharmaceuticals Cherry Hill, NJ Quality Lab Associate I BS/BA in microbiology or biology Exp: 0-2 years pharma experience |
Perform functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. Responsibilities include: Ensure Environmental Monitoring (EM) of the facility’s controlled areas is performed as required. Document EM testing into the EM database prior to incubation, ensure samples are correctly incubated, and record sample results in the EM database following incubation. Compile trending data for EM testing to support investigations. Audit personnel aseptic technique in controlled areas including during process simulations (media fills). | 4/13/2019 |
| 15606 | Wright Medical Alpharetta , GA Assoc Product Development Engineer BS in mechanical or biomedical engineering Exp: 1-2 years in product development |
This entry level engineering position supports the design, development, and evaluation of new product concepts, as well as the redesign or enhancement of existing products. The position may also involve the development of assembly processes and support of equipment and fixtures. Duties include: Writing test protocols and reports. Perform product testing. Assemble prototypes for test and evaluation of new and existing medical devices. Provide technical engineering assistance and interpretation to other departments | 4/13/2019 |
| 15607 | Wright Medical Sacramento, CA Associate Sales Representative, Upper Extremities BS in related discipline Exp: 0-2 years |
This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. You will: Conducts regular sales calls in person to develop customer relationships and follow up on leads in order to promote, market and sell products.Prospects for new accounts and seeks opportunities to increase sales with existing customers.Listens to customer needs and suggests appropriate products/solutions. | 4/13/2019 |
| 15608 | Wright Medical Memphis , TN Assoc Global Demand Planner BS/BA in finance, supply chain, or related Exp: 0-1 years |
The Global Demand Planner will proactively analyze, recommend and challenge finished goods unit forecasts, inventory policies, and safety stock strategies based on market demands and business goals. This individual will also be responsible for facilitating proactive, cross-functional management of Global Supply Chain investments through Life Cycle Management (LCM) in the product development process. You will: Deployment of the optimum techniques to improve forecast accuracy given the demand stream characteristics observed. Identify and analyze demand trends and incorporate in forecasting, and facilitate safety stock strategies with newer brands to achieve inventory objectives for assigned products. | 4/13/2019 |
| 15609 | Wright Medical Alpharetta , GA Cartiva Quality Control Inspector HS Diploma, BS/BA Exp: 1+ years in FDA/ISO environment |
The Quality Inspector is responsible for performing inspection activities of both sterile and non-sterile products to ensure compliance to current specifications and procedures. Activities include Device History Record review, examination of supplier provided data, labeling and product acceptance, ensuring nonconforming product is identified, documented and segregated from acceptable product. Maintain control of quarantine area to ensure unintended use. This position is also responsible for handling and segregation of returned product. | 4/13/2019 |
| 15610 | WuXi AppTec St. Paul, MN Associate Quality Assurance Specialist BS/BA Exp: 0 years |
The Associate Quality Specialist is responsible for ensuring GLP studies, GMP testing, and GMP manufacturing activities are executed in accordance with the appropriate regulatory bodies and internal procedures. Responsibilities include: Ensures compliance to Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP). Perform job specific tasks in compliance with applicable Regulations, International Standards, and WuXi AppTec Policies and Standard Operating Procedures.Reviews final reports (GLP), batch records (cGMP), Certificates of Analysis (GMP), and/or other necessary documentation, as appropriate to the defined Quality Role within the applicable regulation(s). | 4/13/2019 |
| 15611 | WuXi AppTec St. Paul, MN Associate Sample Coordinator AS/AA in biosciences Exp: 1+ years lab experience |
This position is responsible for processing samples for assigned tests in compliance with GLP, GMP, and ISO standards including test sample log in and accountability. Responsibilities include: Provides operational support for Sample Preparation/Sample Receipt activities, including but not limited to media preparation, cleaning, equipment/materials staging, and use of aseptic technique. Receives incoming samples and reviews them for integrity to ensure they are sufficient for testing. Coordinates time and resources to ensure efficient processing of incoming projects. Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required. | 4/13/2019 |
| 15612 | WuXi AppTec St. Paul, MN Associate Chemistry Specialist BS/BA Exp: 0 years |
The Associate Chemistry Specialist will perform a variety of testing preparation techniques, including sample preparations/extractions, reagent preparation procedures and solvent exchange. The position will also include performing a variety of routine benchtop and analytical analysis. Responsibilities include: Perform benchtop testing, including pH, non-volatile residue, conductivity, and other entry level techniques. Extract test samples using soxhlet, submersion, and fluid path techniques. May assist scientists and other specialists with various supporting procedures, such as sample vialing, reagent preparation, and solvent exchange. | 4/13/2019 |
| 15613 | WuXi AppTec Philadelphia, PA Laboratory Technician II BS/BA in biological sciences or related Exp: 1-2 years |
Performs Cell Culture and Cell-Based assays (BSL2 and BSL2+) according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Completes batch records and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs daily work activities with minimal supervision. | 4/13/2019 |
| 15614 | WuXi AppTec Philadelphia, PA Associate Warehouse Coordinator HS Diploma Exp: 1+ years |
Performs all aspects of receiving and internal deliveries to end users. Responsibilities include: Responds to receiving, delivery requests in a timely and professional manner. May help with Shipping as needed. Contacts vendors to retrieve proper quality documentation such as: Certificate of Analysis. Participates in End of Month (EOM) inventory. May participate in preparing shipping paperwork with accuracy, as well as completes shipping transaction in appropriate system (UPS etc.) as needed. | 4/13/2019 |
| 15615 | WuXi AppTec Philadelphia, PA Research Associate, Analytical Development - Molecular Biology BS/BA in biological sciences or related Exp: 1+ years |
Performs research & development activities and assay validations as required under direct supervision. Drafts test methods and clearly documents all experiments according to SOPs and cGMP guidelines. Performs laboratory maintenance duties. Works closely with Testing Operations during assay transfer and validation activities. | 4/13/2019 |
| 15616 | WuXi AppTec Plainsboro, NJ Research Associate II AS or BS/bA in life sciences Exp: 1-3 years |
WuXi AppTec is searching for a Research Associate in a growing Immuno Oncology Group. Responsibilities include: Conducting in vivo pharmacology experiments for preclinical contract research with minimal supervision. Assisting and performing efficacy and PK-PD studies and developing new in vivo/ ex vivo assays and models with minimum supervision, as needed. Help to design, optimize and execute of pharmacology experiments for compound screening, compound mode of action and efficacy in mechanistic and disease models, e.g. syngeneic and xenograft tumor model, acute and chronic autoimmune/inflammatory conditions, and analyses and reporting of experiments or implantation, blood/tissue collection, etc | 4/13/2019 |
| 15617 | Xbiotech USA Austin, TX Manufacturing Associate I-Downstream BS/BA in life sciences or health care Exp: 0-2 years |
Perform all activities associated with supporting downstream production of our clinical and commercial operations in a GMP manufacturing setting. One must be flexible to work multiple shifts and weekends and/or overtime as needed. Perform downstream operations including: column chromatography, sterile filtration. and viral filtration. Assist manufacturing team in final drug product processes (Formulation and Aseptic Fill). Perform setup and operation of chromatography processing equipment according to established Standard Operating Procedures (SOP’s) and/or Master Production Records (MPR’s). This equipment may include but is not limited to AKTAprocess skids. | 4/13/2019 |
| 15618 | Xellia Pharmaceuticals Raleigh, NC Production Operator I HS Diploma Exp: 1-3 years |
The incumbent will be responsible for the operation of various types of processing and test equipment in environmentally controlled areas per Standard Operating Procedures. This includes but is not limited to: steam sterilizers, vial/parts washers, dehydrogenation tunnel, formulation tanks and associated equipment, analytical balances, pumps, filter test equipment and other associated equipment. As part of these responsibilities, the Production Operator I monitor cycles and reviews data to ensure requirements have been met and completes all associated documentation. | 4/13/2019 |
| 15619 | XenoTech Kansas City, KS Research Assistant BS in chemical or biological sciences Exp: 1+ years lab experience |
The Research Assistant assists with routine laboratory functions including diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintains inventory of supplies, and various other responsibilities. These include: Design and conduct routine and atypical experiments. Maintains laboratories and equipment and performs minor repairs on equipment, with supervision. Maintains appropriate logs, records and study notebooks. Adheres to Good Laboratory Practice regulations and Sekisui XenoTech safety policies and procedures | 4/13/2019 |
| 15620 | Zimmer Biomet Palm Beach Gardens, FL Mfg Engineer BS in engineenering Exp: 0-3 years |
The manufacturing engineer is responsible for providing manufacturing engineering services to support efficient manufacturing processes. Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. Duties include: Maintaining and improving controlled technical documents such as prints, procedures, bill of materials and routers. Supporting a wide variety of processing applications such as machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc. Conducting feasibility study to estimate product cost and analyze capital equipment, capacity, and capability requirements. | 4/13/2019 |
| 15621 | Zimmer Biomet Parsippany, NJ Development Engineer BS from ABET accredited school in engineering Exp: 0-3 years |
Responsible for the design, development, and processing of implants and instruments. Work is expected to encompass both the development of new products and maintenance of existing products. Position will lead development aspects of the project as a core team member. Responsibilities include: Leads the development of new products and manufacturing processes. Identifies all tasks required to complete project assignments according to Design Control procedures. Prepares work plans outlining estimated manpower requirements and development costs. Recommends project budget and schedule to carry out programs on a timely basis. | 4/13/2019 |
| 15622 | Zimmer Biomet Warsaw, IN Quality Engineer BS in engineering Exp: 0-3 years |
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. Duties include: Formulates procedures, specifications, and standards for Zimmer products and processes. Develops and implements corrective/preventative action plans. Collects and analyzes data for gauge and product evaluation. Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products. | 4/13/2019 |
| 15623 | Vedanta Cambridge, MA Contract - Research Associate - Molecular Biology BS or MS in biology or related Exp: 1+ years |
The research associate will work in collaboration with the Microbiology, Immunology, and Systems Biology teams to aid in the characterization of organisms from the human microbiota through the execution of molecular biology assays and next-generation sequencing. General tasks will involve DNA extraction, sequencing library preparation, PCR and PCR-product verification, qPCR, sample organization, and coordination of tasks with the microbiology and immunology teams. Additionally, the research associate will support the preparation of samples for DNA sequencing at Vedanta and off-site. | 4/12/2019 |
| 15624 | Veeva Columbus, OH QA Engineer (CRM) BS in math or computer sciences Exp: 0-5 years |
Veeva Systems is looking for an energetic and enthusiastic Engineer to join our rapidly growing team. This is a hands-on position for delivering a quality SaaS product. As part of Veeva CRM Multi Channel software QA team, you will be given an opportunity to test a high quality product that was built from scratch. Responsibilities include: Participate in product and feature designs with developers, usability specialists, user interface designers, and product managers. Build effective test cases that are used for manual and automation testing. Develop deep expertise in the product | 4/12/2019 |
| 15625 | Veeva Pleasanton, CA Associate Software Engineer, New Grad BS in computer sciences or related Exp: 0-1 years (new grad) |
You’re a front-end, back-end, or mobile software developer (including iOS and Windows Tablet) who likes to work on small teams in a fast-paced, agile environment, releasing features every four weeks. Help us design our solutions. Contribute to technical and functional design decisions, troubleshoot and provide technical product support, and be responsible for all aspects of the software development lifecycle. Drive all aspects of the software development cycle: design, implementation, tuning, testing, and monitoring of the functional areas that you will own, delivering products within the schedules and timelines. | 4/12/2019 |
| 15626 | Veeva Pleasanton, CA Associate QA Engineer, New Grad BS in applied math, information systems, or related Exp: 0-1 years (new grad) |
You’re a Quality Engineer who likes to work on small teams in a fast-paced, agile environment, releasing features every four weeks. You will help us ensure there is quality in our design implementation. You will contribute to technical and functional testing, understand the areas that need troubleshooting more than other areas, and be part for all aspects of the software development lifecycle. Drive all aspects of the software development test cycle: testing the design and the implementation of the code, driving automation and monitoring of the functional areas that you will own, delivering quality products within the schedules and timelines. | 4/12/2019 |
| 15627 | Veeva Pleasanton, CA Associate Performance Engineer, New Grad BS in computer sciences or related Exp: 0-1 years (new grad) |
The Vault Performance Engineering Team works within the Vault Development Team and participates in all phases of the SDLC. In this role you will: Collaborate with Vault team members in Product Management, Engineering Management and Quality Assurance to help design and develop performance tests. Test new features pre-production to make sure they will scale and perform. Implement and execute load tests in JMeter. Use and update Python scripts for managing test systems. | 4/12/2019 |
| 15628 | Veeva Multiple locations, Associate Consultant, New Grad BS/BA Exp: 0-1 years (new grad) |
You will work on project teams implementing Veeva’s cloud software applications. Participate in business process discovery workshops, gather requirements, configure the solution, help with testing and final deployment. Explain solutions to a variety of audiences and provide subject matter expertise on Veeva applications and technical design. | 4/12/2019 |
| 15629 | Veracyte South San Francisco, CA Laboratory Automation Engineer BS or MS in biological sciences or computer sciences Exp: 1+ years |
We are seeking a new Automation Engineer to perform technical support on our lab instrumentation in our collaborative, high-energy work environment. S/he will be responsible for supporting the installation, modification, upgrade, and validation of lab equipment. Other key aspects of the role include: Support the development, test, and implementation of automated assays to increase the operational and throughput efficiencies in the laboratory in conjunction with technical leadership, regulatory managers, and professional leadership. Work as an independent contributor, working with cross functional teams focused on the development of automated clinical assays. Collaborate with the Bioinformatics and/or Information Technology (IT) team to integrate automated laboratory solution data outputs into departmental systems such as Laboratory Information Management Systems (LIMS) | 4/12/2019 |
| 15630 | Veracyte South San Francisco, CA Lab Assistant - Accessioning AS or BS/bA in life sciences Exp: 1+ years |
The Lab Assistant - Accessioner will perform routine specimen accessioning in accordance with established protocols. The position will process specimens upon receipt in the lab. Additional responsibilities include all related clerical functions, lab maintenance and regulatory compliance tasks. You'll work alongside a highly engaged team of Lab Assistants and Clinical Lab Scientists and will collaborate with other groups across Veracyte. You'll have the opportunity for ongoing training, competency assessments and sharing ideas for continuous improvement in the lab. The work schedule is Tuesday - Saturday. | 4/12/2019 |
| 15631 | Verb Surgical Mountain View, CA Project Coordinator - Contract BS in engineering Exp: 0-5 years |
Support Senior Project Manager on program critical project. Smooth is fast, and we need to go fast. Get to see what it takes to build a surgical robot. Key accountabilities include: Update Program Milestones in a PERT and Gantt charts. Place purchase requisitions. Create graphics to communicate plans, status, risk to the team and management. | 4/12/2019 |
| 15632 | Vericel Cambridge, MA Quality Control BS/BA Exp: 1+ years in cGMP lab |
Quality Control (QC) is responsible for incoming inspection of components and raw materials, plus quality testing (e.g. analytical, microbiological) of intermediate, stability and final product samples to demonstrate that all products manufactured meet standards required for cGMP operations. Various techniques (e.g. assay transfers, validation and qualification of new instrumentation) are utilized within the Quality Control Laboratory to ensure cGMP compliance. | 4/12/2019 |
| 15633 | Veristat Remote Work, Clinical Research Associate (Oncology) BS/BA in life sciences or health care Exp: 1+ years in clinical monitoring |
As a Clinical Research Associate You Will: Manage and monitor clinical trial activity, including conduct of all monitoring visits at investigator sites and ensure all regulatory, ethics and training requirements are met. Responsible for ensuring that data will pass international quality assurance audits and regulatory inspections. Assist the project manager with the preparation of study tools, presentations and training material for investigator meetings, site qualification visits and site initiation visits as required. Work with the Management team in the development/revision and implementation of Standard Operating Procedures as required. Ensure compliance with appropriate Sponsor and Veristat SOP’s, 21CFR/ICH guidelines and applicable regulatory requirements. Ensure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Sponsor and Veristat values. Required to travel 60-80% on average | 4/12/2019 |
| 15634 | Veristat Montreal, Qu Cliniacl Research Associate BS/BA in life/health sciences Exp: 1+ years in clinical monitoring |
As a Clinical Research Associate You Will: Manage and monitor clinical trial activity, including conduct of all monitoring visits at investigator sites and ensure all regulatory, ethics and training requirements are met. Responsible for ensuring that data will pass international quality assurance audits and regulatory inspections. Assist the project manager with the preparation of study tools, presentations and training material for investigator meetings, site qualification visits and site initiation visits as required. Work with the Management team in the development/revision and implementation of Standard Operating Procedures as required. Ensure compliance with appropriate Sponsor and Veristat SOP’s, 21CFR/ICH guidelines and applicable regulatory requirements. Ensure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Sponsor and Veristat values. Required to travel 60-80% on average | 4/12/2019 |
| 15635 | Vicarious Surgical Charlestown, MA Quality Engineer BS/BA in engineering Exp: 0-4 years |
Reporting to the Director of Quality Systems, as a Quality Engineer you will help develop, maintain and enforce all aspects of the quality system from the ground level. The quality engineer will work alongside and in parallel with the product development, manufacturing and regulatory teams, improving what we already have and imagining what we don’t. We are looking for talented quality engineers who are excited to lead and assist in the development and maintenance of Vicarious Surgical’s quality system. Support ISO, and MD certification process and compliance to FDA regulations by leading and/or assisting in the development, implementation, monitoring, enforcement and improvement of the quality system. Prepare, evaluate and critique technical documentation including design justifications and rationales based on sound scientific or engineering principles. | 4/12/2019 |
| 15636 | Viracor Eurofins Lee's Summit, MO Research Scientist I BS/BA Exp: 0-3 years lab experience |
The Research Scientist is primarily responsible for conducting research, development, validation and execution of assays to meet the development requirements within corporate/client timelines and cost objectives. Learn new techniques and instrumentation, Implement research plans, designs and testing protocols , Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results , Keep accurate documentation of all research project steps according to Viracor Eurofins regulatory guidelines | 4/12/2019 |
| 15637 | Viracor Eurofins Lee's Summit, MO Quality Assurance Specialist I HS Diploma Exp: 1-2 years in regulated environment |
The position is primarily responsible for Quality Management System (QMS) activities and compliance with applicable regulatory requirements by ensuring the effectiveness of the QMS in meeting its stated goals and objectives. This position is also responsible for the management and maintenance of the electronic document management system, including training staff on document control processes and procedures. This position is also responsible for managing both paper and electronic records to ensure that controlled records are created, identified, changed, reviewed, retained, stored, and maintained in a manner that meets requirements. | 4/12/2019 |
| 15638 | Viracor Eurofins Lee's Summit, MO Laboratory Data Entry I HS Diploma Exp: 0-2 years |
The Laboratory Data Entry Associate is primarily responsible for performing duties related to accessioning and data entry with a high degree of proficiency. Duties include: Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other specimen tracking system. Examine samples for accuracy and other requirements (sample type, volume, etc.). Make appropriate internal or external contact to resolve patient demographic issues or discrepancies | 4/12/2019 |
| 15639 | Viracor Eurofins Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in sciences Exp: 1+ years lab experience |
The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Duties include: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. | 4/12/2019 |
| 15640 | Viracor Eurofins Lee's Summit, MO Clinical Laboratory Scientist (CLS) Coordinator BS/BA in sciences Exp: 1+ years clinical lab experience |
The CLS Coordinator is primarily responsible for coordination of designated operations and/or projects within the clinical laboratory. Responsibilities include: Demonstrate outstanding competency within all trained areas of the Clinical Laboratory Scientist. Evaluate and maintain inventory to ensure continuous service to the clients without creating over-stock. Assist Supervisor or Manager in overseeing the maintenance and record keeping for all instrumentation within the section. | 4/12/2019 |
| 15641 | Viracor Eurofins Lee's Summit, MO Research Technician BS/BA in sciences Exp: 1+ years lab experience |
The Research Technician is primarily responsible for performing laboratory tests and analyses under the direction of a lab manager or research scientist. Duties include, but are not limited to, specimen management, specimen pipetting, instrument operation/maintenance, data entry, specimen storage, following Standard Operating Procedures (SOPs) and ensuring all laboratory equipment and work areas are clean, sterile, and in proper working order. Applicant may be responsible for calibration of instruments and conducts routine tasks as directed. Works under moderate supervision with some latitude for independent judgment. | 4/12/2019 |
| 15642 | Virbac St. Louis, MO Pharmaceutical Operator - Level 1 HS Diploma Exp: 1-3 years in production |
Operate filling and packaging production unit for FDA and EPA regulated and less regulated pharmaceutical products. Assignment includes: Organize activity for production, preform equipment set-ups and adjustments, preform line clearances, and monitor key lines. | 4/12/2019 |
| 15643 | Express Scripts Indianapolis, IN Pharmacy Technician- Accredo HS Diploma Exp: 0-1 years |
As a member of our fulfillment team, you’ll work in one of our pharmacy distribution facilities, which are responsible for filling and shipping over 90,000 prescriptions a day. These state-of-the-art facilities are climate controlled, well-lit, and use a wide variety of technology to help you perform at peak productivity levels. Job functions include: Process requests for new and refill prescriptions. Select and retrieve appropriate medications. Verify quantities and prepare labels for bottles. Send orders to pharmacy staff for completion and verification of prescription based programs. Select appropriate packing materials and prepare packages for shipment. | 4/11/2019 |
| 15644 | Express Scripts Tempe, AZ Patient Care Adovacate HS Diploma Exp: 0-1 years |
Handle customer service inquiries from members, providers, physicians and internal and external clients related to pharmacy benefits. Work to research and resolve problems in a timely manner. Assist members in understanding and maximizing the use of their pharmacy distribution program. Use computerized system to gather information and respond to questions. Document issues and resolutions in a common database. Escalate issues as necessary. | 4/11/2019 |
| 15645 | Express Scripts Mississauga, On Pharmacy Assistant Exp: 0-3 years in retail pharma |
The Pharmacy Assistant works closely on a daily basis with the Member Contact Centre and the Pharmacy to process member prescription requests. The Pharmacy Assistant will be responsible for processing prescription refills through Kroll and responding to and taking action on member requests as appropriate within his/her scope of practice. Duties include: Accurately process prescriptions through Kroll including third party adjudication and rescheduling of next fill. Recording and maintaining member information in the CRM system. Answering questions from patients and/or resolve customer issues according to Ontario College of Pharmacist’s regulations. | 4/11/2019 |
| 15646 | Express Scripts Tampa , FL Patient Care Adovacate HS Diploma Exp: 0-3 years |
Handle customer service inquiries from members, providers, physicians and internal and external clients related to pharmacy benefits. Work to research and resolve problems in a timely manner. Assist members in understanding and maximizing the use of their pharmacy distribution program. Use computerized system to gather information and respond to questions. Document issues and resolutions in a common database. Escalate issues as necessary. | 4/11/2019 |
| 15647 | Express Scripts St. Louis, MO Benefit Validation Analyst MS in relavent field Exp: 0-3 years |
The Testing Analyst II is responsible for the management of new and existing client testing to validate benefit set-up based on client's intent and expectation. The role analyzes client intent and creates validation and test scenarios, executes validations/tests and analyzes results. This will cover all functions necessary to implement a client, including, but may not be limited benefits, clinical, pricing, and coverage for all lines of business in scope for benefit validation (Health Plan clients, commercial clients, MedD clients, book of business projects, etc.). The role will require considerable cross-functional communication to effectively monitor the daily status of client implementations and plan changes. This role collaborates with internal partners to obtain necessary information to perform the work, request intent clarifications, identify setup issues, and bring closure to our validation/testing activity. | 4/11/2019 |
| 15648 | Express Scripts Greensboro, NC Pharmacy Technician- Accredo HS Diploma Exp: 0-1 years |
As a member of our fulfillment team, you’ll work in one of our pharmacy distribution facilities, which are responsible for filling and shipping over 90,000 prescriptions a day. These state-of-the-art facilities are climate controlled, well-lit, and use a wide variety of technology to help you perform at peak productivity levels. Job functions include: Process requests for new and refill prescriptions. Select and retrieve appropriate medications. Verify quantities and prepare labels for bottles. Send orders to pharmacy staff for completion and verification of prescription based programs. Select appropriate packing materials and prepare packages for shipment. | 4/11/2019 |
| 15649 | Unchained Labs Pleasanton, CA Lab Technician AS or BS in biochemistry, chemistry or related Exp: 1+ years |
Responsibilities as a lab technician include: Receive, document,and prepare customer samples for testing, visual inspections of samples, test plans and reports, preforming method development and validations, coordination of the maintenance/operations of lab equipment. | 4/11/2019 |
| 15650 | United Theraputics Research Triangle Park, NC QA Specialist I - Training and Documentation BS in sciences Exp: 1+ years |
The QA Specialist I – Training & Documentation assists in the execution of GXP Documentation and Training processes and the system administration of the associated Learning Management System (LMS) and electronic Document Management System (eDMS). Manages tasks associated with New Employee training and filing documents. Ensures compliance to applicable company policies, standards and regulations. Support and conduct New Employee Orientation (NEO) training and provides training support for UT and UT subsidiaries, as applicable. Controls and maintains training document and document files. Collect training records, checks for accuracy, completeness, and obtains corrections when necessary. | 4/11/2019 |
| 15651 | United Theraputics Manchester, NH Research Associate I/II - Biomaterials BS/BA in biomedical or chemical engineering Exp: 1+ years |
Support Biomaterials by performing research and development engineering in materials design, printing, cellularization, and characterization of 3D printed scaffolds. Duties include: Assist in development and characterization of 3D printing under the direct supervision of project leaders/scientists. Assist materials development to optimize cellularization of printed objects. Build and maintain an understanding of current and emerging technologies within the field of biomaterials. Assist in performing analytical techniques for material development and characterization of 3D printed scaffolds. Follow prescribed laboratory methods and protocols under GLP/GMP-conditions; laboratory safety and use of protective equipment, and handling of biohazard materials including human or animal cells and tissues | 4/11/2019 |
| 15652 | United Theraputics Manchester, NH Research Associate I/II - 3D Printing BS/BA in biomedical or chemical engineering Exp: 1+ years |
Support 3D Printing by providing expertise regarding operation and optimization of workflow. Responsibilities include: Validate pending design decisions by building and analyzing proof of concept prototypes. Design and implement test setups, relating results back to physical printer behavior and changing print parameters to optimize print quality. Assist in performing analytical techniques for material development and characterization of 3D printed scaffolds. Follow prescribed laboratory methods and protocols under GLP/GMP-conditions; laboratory safety and use of protective equipment, and handling of biohazard materials including human or animal cells and tissues | 4/11/2019 |
| 15653 | Astellas Seattle , WA Research Associate 2, Cell Differentiation MS in sciences Exp: 0-2 years |
This person will acquire further versatility in routine procedures, more technical knowledge, and more understanding of administrative operations, some troubleshooting. They will assist with more complex laboratory operation projects, and will take on more responsibility to provide content for various documents and reports. They will be able to execute protocols with some guidance, and will have ability to summarize results independently. Duties include: Culture and differentiate edited pluripotent stem cell lines into mature hematopoietic and immune cell types. Phenotype differentiated cells using flow cytometry, imaging and gene expression analyses. | 4/11/2019 |
| 15654 | Astellas Seattle , WA Quality Control Associate 2 MS in sciences Exp: 0-2 years lab experiences |
The Quality Control Associate 2 will work to provide cross-functional support for the Technical Operations team by evaluating manufacturing products for product safety and quality. Growing technical knowledge and continued understanding of quality operations with ability to troubleshoot and solve technical problems. Independently contribute to the development of new testing methods. Continues to take on more responsibility to provide content for various documents and reports. Will be able to execute protocols and summarize results with guidance. Will acquire versatility in quality control procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 4/11/2019 |
| 15655 | Upsher-Smith Maple Grove, MN R&D Documentation Specialist MS in life sciences Exp: 0-3 years |
The R&D Documentation Specialist will be a self-motivated individual with experience in authoring regulatory submission documents as well as creation and/or revisions of manufacturing documentation in accordance with GMP standards. He/she will have: (a) demonstrated experience with authoring, editing and controlling of manufacturing batch records (MBR) and process study protocols to support pharmaceutical development activities in Research and Development (b) hands-on experience with authoring and editing of CMC submission documents for ANDAs and/or NDAs (c) experience with creation and revisions of report templates, work instructions and/or standard operating procedures (SOPs) that support R&D activities (d) demonstrated flexibility to support multiple activities within the team/department (e) ability to work closely with cross-functional R&D, Technical Services and Operations team members and mange timelines (f) excellent writing and interpersonal skills. | 4/11/2019 |
| 15656 | Vector Lab Burlingame , CA Histotechnologist/Quality Control Associate I BS/BA in biochemistry, life sciences, or related Exp: 0-2 years |
Vector Laboratories is seeking a Histotechnologist/Quality Control Associate I who will analyze in-process materials, raw materials, finished goods, and stability samples following established operating procedures. The individual may also be required to analyze samples from the research and development department using established testing procedures as per instructions. S/he may also be responsible for helping to organize and maintain laboratory reagents/supplies. The QC Associate I will operate and maintain common laboratory equipment as per instructions and will assist in inventory management as needed. Technical knowledge should include strong knowledge of general laboratory safety and practices and basic understanding of QC principles. This position works under immediate supervision and relies on instructions and established procedures to perform the functions of the job. | 4/11/2019 |
| 15657 | Concerto Health AI Memphis, TN Data Abstractor I AS or equivalent Exp: 0-2 years |
The Data Abstractor navigates electronic medical record systems and other medical databases, reviews medical records, and abstracts medical record data related to specified disease and project requirements. The Data Abstractor works under the direction of the Lead Data Abstractor. Duties include: Access electronic data systems for review of medical records and enter specific data into congruent electronic data systems. Review project specific documents, as needed, to develop familiarity with project goals and with the Abstractor tasks in each project. Use other resources as needed to gain the knowledge required to perform Abstractor work on new projects. Share medical knowledge and project-specific procedural knowledge with other Data Abstractors as needed. | 4/11/2019 |
| 15658 | Thermo Fisher Florence, SC Scientist 1 -PRD BS/BA in chemistry or sciences Exp: 0-3 years |
This is an entry-level opportunity to support the Process R&D efforts at the Florence, SC facility. Responsibilities include: Conduct chemical experiments in laboratory as instructed by a senior staff supervisor. Accurately record and report experiments and scientific findings per assigned departmental standards in a timely manner to meet project objectives. Maintain a clean and safe work environment within the framework of OSHA, cGMP, safety regulations and Thermo Fisher SOPs | 4/6/2019 |
| 15659 | Tmunity East Norriton, PA Associate Process Development Scientist BS or MS in biochemical engineering, chemical engineering, or biotechnology Exp: 0-3 years lab experience or process development |
The Associate Process Development Scientist will perform studies to develop and optimize the manufacturing process of gene-modified cellular products to support the company’s development programs. Under the supervision of Sr. Scientist: Perform development studies including optimization of cell isolation, cell culture, cell transduction and cell cryopreservation processes. Evaluate innovative manufacturing & analytical technologies for engineered T cell manufacturing to improve process efficiency. Author technical and scientific documents including but not limited to SOPs, Master Batch Records, study protocols and reports. | 4/6/2019 |
| 15660 | Tocagen San Diego, CA QA Associate - Document Control BS/BA in life sciences Exp: 1-3 years |
The Quality Assurance Associate is responsible for handling tasks associated with Document Control, including processing, archival, filing, scanning, indexing and formatting new and existing documents within the framework of Veeva Vault Quality Docs software. This position involves familiarity and experience with cGMP Quality System processes and supports all functional areas with needs related to QMS documentation. | 4/6/2019 |
| 15661 | Tolmar Fort Collins, CO Research Assocate I BS/BA in chemistry, biochemistry, or related Exp: 0+ years lab experience |
Under direct supervision, perform sample analysis, data and document review, and method development and validation. Essential duties include: Develop and validate analytical methods to current ICH and USP guidelines. Accurately analyze formulation, drug, or product samples and assist other departments in analyzing samples as requested. Perform routine sample analyses in support of GLP or R&D stability protocols. Assist the Quality Control laboratory in troubleshooting method issues. Exercise technical discretion in the design, execution and interpretation of experiments that contribute to project strategies. Write and review technical reports, summaries, protocols, test methods, standard operating procedures, and other documents for use in the company or for submission to governmental agencies. | 4/6/2019 |
| 15662 | Tolmar Windsor, CO Stability Associate I BS/BA in chemistry Exp: 1+ years |
Responsible for maintaining the following systems and/or databases: Stability System II Software, stability database, stability variances, stability environmental chambers, stability reports, data entry, data auditing and stability records. Other responsibilities include: Requisition, label and place stability samples into appropriate storage conditions according to approved protocols. Enter new lots into the Stability System II Software and stability databases, and audit study start documentation. Pull samples at appropriate time points and deliver to the QC, AD and Microbiology Labs, as appropriate. | 4/6/2019 |
| 15663 | Toxikon Bedford, MA Research Associate, Medical Device Extraction BS/BA in sciences Exp: 0-1 years |
The successful candidate will work hand in hand with our study directors, quality assurance and sponsors/clients to ensure all medical device preparation aspects are performed per scientific and regulatory standards. Responsibilities include: Review the nature and composition of medical devices and determine sample requirements for testing. Medical devices are prepared for testing using geometrical calculations and therefore skill in routine mathematic principles is required. | 4/6/2019 |
| 15664 | Translate Bio Lexington, MA Associate Scientist BS or MS in chemistry or related Exp: 0-6 years |
We are seeking a highly motivated and scientifically rigorous individual to join the Research and Process Development team as an Associate Scientist. The position will report to the Director of the group and will focus on developing novel lipid nanoparticle (LNP) formulations for mRNA delivery. Responsibilities include: Provide formulations and perform characterization assays /data analysis with focus on in vivo studies, drug carrier design/development, assay development etc. Support formulation development activities related to formulation optimization with focus on potency and tolerability. Develop novel formulations for different ROAs. | 4/6/2019 |
| 15665 | Tris Pharma Monmouth Junction, NJ Production Development/Formulation Scientist I MS in pharma sciences Exp: 1+ years in pharma lab |
Product Development R&D Scientists perform preformulation and formulation development activities, prepares formulation batches for compatibility studies, stability studies, Pilot batches and Pivotal batches, perform maintenance of Research and Development (R&D) equipment/instruments. | 4/6/2019 |
| 15666 | Tris Pharma Monmouth Junction, NJ Scientist – Method Validation MS in chemistry Exp: 1+ years |
We have a unique opportunity for an entry level to intermediate Scientist to perform laboratory analyses in the testing of raw materials for release, in process (IP), finished products (FP) during process validation and stability (ST) samples of test batches and to carry out laboratory work to support method validation activities. This position is located at our Monmouth Junction, NJ facility. Responsibilities include: Operates general analytical instruments during raw material, in process and finished product testing such as HPLC, GC, UV/Vis, automatic titration, IR, AA, TLC and dissolution apparatus. Performs wet chemistry tests such as LOD, pH, and titration; prepares standard and sample solutions as required by the test methods; and performs all necessary calculations associated with the test analyses. | 4/6/2019 |
| 15667 | Tunnell Boston, MA Research Associate BS/BA Exp: 0-3 years |
Responsible for the execution and analysis of experiments and analytical procedures. Displays an investigative or technological orientation in designing, executing and interpreting experiments and analytical procedures. Investigates basic technical problems and performs routine scientific procedures and experiments under general supervision. Plans and prioritizes concurrent experimental procedures. Integrates, complies, and tabulates data and assists supervisor in the analysis and interpretation of the results. May provide oral presentations on results to other department members. Works under active supervision. Follows established procedures. Work is reviewed for soundness of technical judgment and overall adequacy and accuracy. Contributes to the completion of milestones associated with specific projects. Failure to achieve results or erroneous execution may cause delays in program schedules, and may result in the allocation of additional resources. Frequent internal company contacts. Infrequent inter- departmental and outside constituent contacts on routine matters. Experience: 0 to 3 years. | 4/6/2019 |
| 15668 | Tunnell King of Prussia, PA Analyst BS/BA in engineering Exp: 0-4 years |
As an analyst, you will be part of teams that work across the entire spectrum of our offerings and our clients. We are working with some of the most innovative companies, who are providing the latest in critically needed therapies. | 4/6/2019 |
| 15669 | Steris St Louis, MO Entry Level Manufacturing Coordinator Vocational or AS degree Exp: Entry Level |
Responsible for knowing, understanding, and supporting the STERIS Safety Philosophy. Provides accurate and timely documentation and support to all Production Operations departments. Analyze inventory reports to assure accurate reporting of labor and materials. Compiles and reviews batch records for completeness. Identifies and corrects inaccuracies prior to forwarding to Quality Systems. Accountable for delays in release and meeting expectations for release times. Mentors plant employees and supervisors on documentation compliance and inventory accuracy. Proper execution of assigned duties has a direct impact on the efficiencies of the plant and the final customer’s satisfaction. Contributes to lean transformation by participating on rapid improvement implementation teams. Other duties assigned by Supervisor to contribute to the support of all Production Operation departments. | 4/5/2019 |
| 15670 | Steris Chicago, IL Sterile Processing Technician HS Diploma or GED Exp: 0-1 years in SPD |
Provides on-site support for the reprocessing of surgical instruments and trays to contracted facilities in compliance with the Department of Health, TJC, OSHA, CDC, AAMI and AORN standards and facilities goals and policies. Position level will be determined by previous job related experience, performance and certification requirements. | 4/5/2019 |
| 15671 | Stratos Genomics Seattle , WA Lab Assistant –Nanotechnology/ Molecular Biology BS/BA in bioengineering, biochemistry, or related Exp: 1+ years lab experience |
The laboratory assistant will have opportunities to gain experience with meaningful data analysis, thinking critically & objectively, sample preparation, SOP optimization, and experimental design. Responsibilities include: Inventory, prepare, and maintain components for the sequencing platform. Maintain a clean, safe, and organized laboratory. Perform experiments on the sequencing platform as outlined by manager. Communicate results, status updates, and SOP deviations clearly and effectively to manager. Understand the purpose of each procedural step and how it affects downstream results. | 4/5/2019 |
| 15672 | Stratos Genomics Seattle , WA Research Associate—Molecular Engineering BS/BA or MS in chemistry, chemical engineering or related Exp: 1-2 years lab experience |
Candidates will be involved in synthesizing our unique building blocks for our novel DNA sequencing technology, Sequencing by Expansion, developing and optimizing synthesis protocols as well as proposing and executing innovative experiments to push our technology forward. Functions include: Plan and execute complex projects including; communicating schedule, identifying necessary resources, implementing steps, and keeping projects on track. Design and execute well-controlled experiments. Perform data analysis and protocol development. | 4/5/2019 |
| 15673 | Stratos Genomics Seattle , WA Scientist/Research Associate, Nanotechnology/Molecular Biology BS/BA or MS in chemistry, chemical engineering or related Exp: 1-5 years lab experience |
Candidates will be involved in developing and optimizing the nanopore-based detection platform for our novel DNA sequencing technology, Sequencing by Expansion. The position primarily involves hands-on laboratory work as individual contributors and as a part of a development team. The Research Associate will work directly with founding Technical and Scientific Officers, Scientists, and Research Associates in a dynamic start-up biotech environment. Responsibilities include: Plan and execute complex projects, communicating schedule, implementation steps, and progress, Design and execute well-controlled experiments, Perform data analysis and protocol development, Identify problems and propose solutions | 4/5/2019 |
| 15674 | Stryker Portage, MI Design Engineer – Application Software - NSE BS/BA in computer sciences, engineering or related Exp: 0-5 years in design engineering |
As a Design Engineer (Application Software) is responsible for the software system design of their product or subsystem from start to finish. You will provide design creation concepts to a new product development project to ensure design alignment with overall scope. Working in a cross functional team is a guarantee. Navigating your way through technical design discussions and ensuring appropriate analysis of decisions through application of sound engineering judgment and risk analysis will be the normal. | 4/5/2019 |
| 15675 | Stryker Virtual, MN Manufacturing Engineering Technician AS or BS/BA Exp: 0-2 years |
Focus on manufacturing floor support. Also, work with Operations/Process Development teams (assembly staff, engineers, and management) to ensure that production objectives are achieved with a constant drive for continuous improvement. These objectives include: aid in the efficient implementation and analysis of processes, process flow and equipment. Work with engineers on continuous improvement opportunities for facility layout and production flow optimization. | 4/5/2019 |
| 15676 | Stryker Fort Lauderdale, FL Assembly Technician I in Fort Lauderdale HS Diploma or GED Exp: 1+ years |
Responsible for providing assembly, testing and facility support for all our production efforts. Assembly of fabricated parts and assemblies at work stations along with testing of final assemblis to meet tolerances and product specifications. Uses hand tools and power tools to assemble units according to assembly / work instructions. Relies on instructions and pre-established guidelines to perform the functions of the job. Basic skills with moderate level of proficiency. Works under minimal supervision, requires exercising some independent judgment and may be called upon to provide training to new employees | 4/5/2019 |
| 15677 | Stryker Cary, IL Marketing Product Associate BS/BA Exp: 0-3 years in marketing/sales |
The Marketing Product Associate manages product line initiatives including, sales support and communication, marketing collateral development, market research, competitive intelligence, technical support and marketing plan development. Responsibilities include: Management of current marketing platforms that support and enable our sales team. Collaborate with internal teammates from across the organization on product management initiatives such as cost savings initiatives and product enhancements. Support implementation of Sage interventions at the hospital level through on site education and sales rep support. | 4/5/2019 |
| 15678 | Stryker Kalamazoo, MI Additive Design Engineer BS in mechanical engineering or related Exp: 0-2 years |
The Additive Design Engineer is a key member of the AO Additive team, focused on developing additive-enabled product designs along with divisional R&D and AO counterparts. The Design Engineer will work as an embedded member of the divisional product development teams and work hand-in-hand on design concepts that lead to new products to be launched from the AO Additive New Product Introduction team. Key responsibilities include: Collaborate with divisional R&D and AO to understand product requirements and use additive design methodologies to improve performance of new and existing products. Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures. | 4/5/2019 |
| 15679 | Sun Pharma Billerica, MA QC Analyst I BS/BA in sciences Exp: 0-2 years |
Performs various quality control tests on raw materials, in-process and final product using established Standard Operating Procedures (SOPs) and working in accord with current Good Manufacturing Practices (cGMPs). Responsibilities include: Performs analytical quality control tests and assays for release, stability, and complaint follow-up on raw materials, in-processing and final products. Performs the quality control tests and assays and monitors equipment (i.e. water systems, environmental chambers). Maintains records of the data in manual logs. Basic training in use of Single Wavelength Ultraviolet/Visible (UV/VIS) Spectrometer, Conductivity Meter, pH meter, Dissolved Oxygen Analyzer, Karl Fischer Titrator, High temperature furnaces and oven, Fume Hoods, Stir/Hot Plates, Propane Burners, Compressed Gas Regulators and Cylinders | 4/5/2019 |
| 15680 | Surmodics Eden Prairie, MN R&D Development Technician Associates Exp: 0-10 years in medical devices |
Provide technical support for catheter-based medical device design and development at SurModics, Inc. Responsibilities include: Fabricate device prototype components and assemblies to assist in the design and development of new catheter-based products. Refine processes in the development of new products while working with the engineering team. Assist with developing and troubleshooting manufacturing processes and equipment, including fixture design and equipment qualifications. Provide technical support for catheter-based medical device design and development at SurModics, Inc. Responsibilities include: Fabricate device prototype components and assemblies to assist in the design and development of new catheter-based products. Refine processes in the development of new products while working with the engineering team. Assist with developing and troubleshooting manufacturing processes and equipment, including fixture design and equipment qualifications. Provide technical support for catheter-based medical device design and development at SurModics, Inc. Responsibilities include: Fabricate device prototype components and assemblies to assist in the design and development of new catheter-based products. Refine processes in the development of new products while working with the engineering team. Assist with developing and troubleshooting manufacturing processes and equipment, including fixture design and equipment qualifications. Provide technical support for catheter-based medical device design and development at SurModics, Inc. Responsibilities include: Fabricate device prototype components and assemblies to assist in the design and development of new catheter-based products. Refine processes in the development of new products while working with the engineering team. Assist with developing and troubleshooting manufacturing processes and equipment, including fixture design and equipment qualifications. | 4/5/2019 |
| 15681 | Surrozen South San Francisco, CA Research Associate, Protein Sciences Group - Molecular Biology/Protein Expression BS/BA or MS in biology, biochemistry or related Exp: 0-2 years in research |
This position is a great opportunity for both experienced associates to expand their skills to accelerate therapeutics discovery for regenerative medicine, and for energetic new graduates with passion for Biotech research in an industrial setting. Responsibiliteis include: Produce recombinant DNA clones using state-of-the-art molecular biology protocols and perform routine plasmid preps. Perform plasmid-transfection into mammalian cells for small to medium scale recombinant protein expression. Follow SOPs and perform modern purification techniques like affinity, and SEC chromatography on AKTA-FPLCs to produce a wide variety of recombinant proteins including antibodies and antibody-based constructs. | 4/5/2019 |
| 15682 | Sword Diagnositcs Chicago, IL Research AssociateI, Product Applications BS/BA in biology or related Exp: 1-3 years lab experience |
Your main responsibilities will be to perform functions in support of Product Application Scientist(s) and other individuals as needed, perform common laboratory testing (including ELISA) using established protocols, prepare buffers and other chemical solutions as needed and use proper personal protective equipment (PPE) and good aseptic technique to handle biological (including human) samples. On a day-to-day basis, you will be expected tosuggest, plan and carry out studies with guidance of supervisor, record data for evaluation, analyze results with guidance of supervisor and assist other lab personnel as needed, maintain organized records of studies performed, and other duties and responsibilities as assigned. | 4/5/2019 |
| 15683 | Syapse San Francisco, CA Associate QA Engineer - Contract BS/BA Exp: 0-1 years in software QA testing |
As an Associate QA Engineer in the System Engineering team, you will work closely with our team to validate the platform and test infrastructure that helps make the data more accessible. Duties include: Work on a System engineering team performing system testing on Syapse products. This will include manual testing and developing automation of UI/Integration tests. Documents results; offers observations or improvements after analysis of test results and overall product quality. Collaborates with the development team on bug fix verification and validation (regression testing) | 4/5/2019 |
| 15684 | Synedgen Claremont, CA Chemical Synthesis Associate BS/BA in chemistry or related Exp: 0-3 years |
Duties as a chemical synthesis associate include: Manufacture active pharmaceutical ingredients, drug products, and medical devices. Ensure compliance with the quality system, regulations, and safety procedures. Maintain instrumentation and facilities in proper operating conditions and cleanliness. Manufacture pilot stage liquid medical device products. Perform analytical testing for manufacturing, qualification, and validation activities. | 4/5/2019 |
| 15685 | Synexus Austin, TX Research Assistant/Medical Assistant BS/BA Exp: 0-1 years |
Assists the Clinical Research Coordinators in their responsibilities by doing the following: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Perform basic lab procedures, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; and Utilizes universal precautions when in contact with possible contaminants, obtains and maintains certification for the handling of potential infectious fluids and maintains safety for self, patient and others around them; | 4/5/2019 |
| 15686 | Synteracts Morrisville, NC Biostatistician MS in statistics, math or related Exp: 0-2 years |
The Biostatistician performs the data analysis with supervision for assigned clinical studies. Works closely with the clinical team, project Sponsor, clinical data manager, other statisticians and programmers to analyze and present the data based on Sponsor specifications. He/she develops, creates, verifies/validates and maintains the programs for assigned projects in compliance with standard operating procedures. Maintains the full-scope of responsibility for assigned projects: ensures on-time delivery, communicates the status of projects to internal teams and project Sponsors, executes quality assurance procedures on work produced by others and ensures statistical analysis is being done according to specifications. | 4/5/2019 |
| 15687 | Synthego Redwood City, CA Laboratory Associate, Night shift AA in chemistry or biology Exp: 1-3 years |
. As a Lab Associate at Synthego, you will join our growing operations team and have direct responsibility for the synthesis and purification of our gRNA products. This role requires a strong attention to detail, a desire to learn and adapt to new processes, and familiarity with safe laboratory practices. This role will combine hands-on laboratory protocols with advanced automation to ensure the timely delivery of high quality products to our customers. Duties include: Synthesize oligonucleotides by following established SOP’s . Practice continuous improvement by contributing ideas and suggestions to new and existing processes. Operate complex robotic systems to manage liquid product through a highly automated workflow | 4/5/2019 |
| 15688 | System1 Biosciences San Francisco, CA Research Associate BS in biological sciences Exp: 0-1 years |
We are seeking a highly motivated and responsible technician to join our team under a full time or part-time contract. Responsibilities would include: Preparation of biological reagents to support cell culture. Sterilization of culture vessels and associated components. Maintenance and troubleshooting of automation equipment. Must be available for limited and compensated work on weekends. | 4/5/2019 |
| 15689 | System1 Biosciences San Francisco, CA Lab Aid BS in biological sciences Exp: 0-1 years |
We are seeking a highly motivated and responsible Lab Aid to join our team under a full time or part-time contract. Responsibilities include: Ordering lab consumables and reagents. Organizing shipping and receiving of consumables and biological samples. Stocking and managing lab inventory. Managing outside vendors for a range of different services (e.g., LN2, CO2, dry ice, lab coat laundry). | 4/5/2019 |
| 15690 | Taconic Germantown, NY Animal Care Technician HS Diploma or GED Exp: 0 years |
The Animal Care Technician 1 will be responsible for providing general support to animal care technicians in a barrier by completing tasks related to supply import, export, general barrier cleaning and basic animal husbandry. Responsibilities include: Ensuring high standards of animal welfare are met. Reporting inhumane treatment regarding animal care, use or abuse. Documenting work performed according to SOP’s. Ordering supplies, loading and unloading containers or supply cylinders. | 4/5/2019 |
| 15691 | Takeda Thousand Oaks, CA Utility Technician HS Diploma or GED Exp: 0-3 years in biotech maintenance or manufacturing |
Under general to minimal supervision, the Utilities Technician will be a skilled craftsperson responsible for performing installation, troubleshooting, maintenance, repair, testing, monitoring and documentation/logs of a wide variety of office, utility and facility equipment/systems used in manufacturing plants, utility plants, analytical labs, and office areas. The Utility Technician will be responsible for completing various quality system and safety documentation. All work must be completed in a safe (in accordance to HRA, JHA, etc), timely manner according to planning and predefined schedules with minimal impact to production while complying with GMP, SOP, CFR and company regulations. | 4/5/2019 |
| 15692 | Takeda Thousand Oaks, CA Manufacturing Associate I HS Diploma or GED Exp: 0-2 years |
Key responsibilities include: Employee maybe required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include: Identifying, handling, generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes. Responsible for Room sanitization, wrapping up components, operating autoclave, performing CIP/SIP of tanks, small parts washing. Visual inspection of lyophilized product vials, Visual inspection of empty vials for glass defects, Visual inspection of empty vials for washout defects, visual inspection of rubber stoppers for defects. Record bioreactor, chart recorder readings, alarm response related to the bioreactor, skid performance, inoculums and emergency response during blackouts. etc. | 4/5/2019 |
| 15693 | Takeda Brooklyn Park, MN Laboratory Technician AS in life sciences w/lab coursework Exp: 1-2 years |
Objectives in this position include: Perform supportive activities for general laboratory operations, laboratory equipment preventative maintenance, sample pull, receipt and delivery. Support the Technical Operations group by performing routine laboratory tasks to facilitate the experiments performed by the associates and scientists. Assist in the general organization of the laboratory and perform some basic administrative tasks such as photocopying/scanning and organizing documents and files. | 4/5/2019 |
| 15694 | Takeda Los Angeles, CA Manufacturing Technician II HS Diploma/GED, or AS Exp: HS: 1+ years, AS: 0 years |
This position reports to Weekend Grave (E) shift. This position is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. He/She is expected to fully participate in both departmental projects and any quality working teams which may be applicable. Under the general direction of the manufacturing lead operator and the overall direction of the supervisor, this position shall be responsible for the hands on execution of all activities in the production area. Activities include manual tasks and operation of automated equipment. He/She has sufficient technical and administrative competence to initiate minor revisions to existing documents, to troubleshoot simple existing procedures, and to contribute to continuous improvement initiatives. | 4/5/2019 |
| 15695 | Takeda Thousand Oaks, CA Quality Analyst I AS in sciences Exp: 0-3 years |
The selected candidate is responsible for performing the day-to-day quality operations for the Quality Assurance (QA) department within the Quality organization, including batch record review on the floor and quality inspection activities associated with BAXJECT III processes. Perform the final review of QA Inspection documentation to support Filled Unlabeled Vial (FUV) and Final Drug Product (FDP) release. Identify and assess quality risks in activities and processes according to regulatory agency requirements and guidelines and Takeda quality practices. Initiate and complete event investigations to identify why a deviation occurred and to minimize/eliminate reoccurrence. Revise documents to drive continuous improvement including streamlining processes and maintaining GMP compliance. Support departmental projects and any quality working teams when required. | 4/5/2019 |
| 15696 | Takeda San Diego, CA Research Associate, Antibody Discovery MS in biology, chemistry, or related Exp: 0-2 years |
The candidate will perform complex research assignments and will be responsible for the discovery and engineering of therapeutic biologics including antibodies, fusions and other platforms. The candidate will communicate results within the Biotherapeutic Engineering team and with cross functional project team members. Responsibilities include: Under minimal supervision, execute discovery and lead optimization projects using display platform technologies with high quality and efficiency. Handle large data sets and analyze the data. Identify hits based on affinity, specificity and potency. Isolate DNA/RNA, analyzing sequencing data. Apply knowledge of antibody function and characterization, conduct repertoire analysis, and V region classification | 4/5/2019 |
| 15697 | Talis Menlo Park, CA Research Associate MS in biology or related Exp: 0-3 years |
The candidate will join the Assay Development group in the R&D division where focus is on molecular assays development such as nucleic acid isolation, purification, amplification and labeling technologies. We are seeking talented, motivated individuals to join a collaborative effort to enable development of rapid diagnostic tests of several pathogens from various clinical specimens. | 4/5/2019 |
| 15698 | Talis Menlo Park, CA Firmware QA Engineer I BS or MS in computer science or engineering Exp: 0-2 years |
Candidate will work closely will with firmware engineers to execute and write test cases for qualifying new firmware and software builds. Candidate will perform root cause analysis on test failures and write detailed bug reports. Create test scripts for automation framework for unit, integration, and life cycle test, preferably in Python, is a plus. Experience in ARM, RTOS, I2c, SPI, UART or CAN preferred. | 4/5/2019 |
| 15699 | Tanvex San Diego, CA QC Associate, BioAssay BS in biology, chemistry, or related Exp: 0-2 years in quality control |
The QC Associate is responsible for routine and non-routine product testing using biochemical methods such. Additional responsibilities include assisting with transferring analytical methods from development into the QC laboratory and test method validation; generating test results and reporting results for the assigned GMP testing in a timely and compliant manner; sample coordination, lab equipment maintenance, QC document management and review. Knowledge of performing cell-based assay, immuno-assays, and/or QPCR assays in a GMP environment is essential. | 4/5/2019 |
| 15700 | TE Connectivity Minneapolis, MN Operations Engineering Manufacturing Proesses Rotation Associate BS in manufacturing or mechanical engineering Exp: 0-2 years |
The program consists of four six month rotations in multiple areas where this core process is utilized and accompanied by a robust technical and leadership curriculum. At the conclusion of the two year program, participants will be candidates for leading technical or management roles across the company in this core manufacturing process. Responsibilities may include: Shadowing, assisting and learning from the global leaders of the Compounding Extrusion, and Finishing Center of Excellence (CoE) and the Digital Factory Center of Excellence (CoE). Learning how to connect processes to our digital factory network, extract digital process information, and build improvement plans to act on what the data shows. Learning the Wire and Tubing Extrusion core manufacturing process and being an advocate of sharing best practices from one plant to another. | 4/5/2019 |
| 15701 | TE Connectivity San Jose, CA R&D/PRODUCT DVL ENGINEER I BS in engineering or mechanical field of study Exp: 1-3 years in mechanical design |
R&D Product Development Engineer is responsible for the development and introduction of new medical interventional products. The R&D Engineer will champion the execution of new products that deliver an exceptional customer experience. Additionally, the R&D Engineer will be responsible for managing project costs, issuing quotes to customers, procuring material quotes and interacting with customers. This role complies to FDA QSR (21 CFR 820), ISO 13485 requirements and adheres to the Quality Management System (QMS).TE Connectivity’s R&D/Product Development Engineering Teams conceive original ideas for new products, introduce them into practice. They are responsible for product development, and qualification from market definition through production and release; assist in the qualification of suppliers for new products to ensure suppliers deliver quality parts, materials, and services for new or improved manufacturing processes; conduct feasibility studies, testing on new and modified designs; direct and support detailed design, testing, prototype fabrication and manufacturing ramp. The R&D/Product Development Engineering Teams provide all required product documentation including, but not limited to, Solid Model, 2D/3D production drawings, product specifications, and testing requirements. | 4/5/2019 |
| 15702 | TE Connectivity Wilsonville, OR PRODUCTION OPERATOR (FINISHING OPERATOR) HS Diploma Exp: 1-3 years |
TE Connectivity's Manufacturing/Production Teams transform raw materials into finished goods and ensure component flow. They perform changeovers and setups according to production schedule, perform quality checks according to established processes and document the results as required by our quality procedures. Every team member is responsible for maintaining housekeeping and organization of the work area as well as following TE Connectivity's EH&S policies and procedures. | 4/5/2019 |
| 15703 | Tedor Pharma Cumberland, RI Production Technician HS Diploma Exp: 1-2 years production environment |
The Production Technician position performs all tasks involved in the pharmaceutical process following cGMP’s and SOP’s such as wet granulation, dry granulation, tablet compression, encapsulation, tablet coating, packaging and finished product, put product on stability. The position follows standard work methods and practices safe work habits to ensure production is as efficient and safe as possible. Perform hands on R&D process/product scale up and production studies on specifically assigned products and projects. Perform cleanings to rooms and equipment, major and minor cleaning, swabs equipment, cleaning verification, confined space entry, lockout tag out. | 4/5/2019 |
| 15704 | Teligent Buena, NJ QC Chemist I BS in chemistry Exp: 0-3 years in pharma or lab experience |
Provide accurate and timely testing of raw materials, finished product and/or stability samples as assigned. Ensure the safety and reliability of products produced in compliance with quality and regulatory requirements. Essential responsibilities include: Perform quality control testing on raw materials, finished product, pre-approval and commercial stability samples as assigned by the supervisor. Wet and Physical chemistry techniques including but not limited to: Karl Fisher, Viscosity, Microscopy, pH, specific gravity, IR, Specific Rotation and wet chemistry. | 4/5/2019 |
| 15705 | Tempus New York, NY Jr. Clinical Data Abstractor BS or MS in genetics Exp: 0-3 years |
We are looking for Jr. Data Abstractors (JDAs) to join our rapidly growing clinical data team. JDAs will be responsible for reviewing clinical records, structuring key data elements and helping to ensure that clinicians who treat cancer patients have access to meaningful data and insights. Responsibilities include: Extract, structure and analyze data to construct the foundation of a cancer genomics database, Work with multiple data sources to extract information to pull into various reports, Maintain highest quality standards through rigorous QA process to identify and correct mistakes and inconsistencies in abstracted data | 4/5/2019 |
| 15706 | Tempus Chicago, IL QA Coordinator BS/BA Exp: 0-2 years |
As a QA coordinator, your responsibilities include: Report significant investigation/deviation issues and system deficiencies to management, as appropriate. Coordinate the internal document control system of standard operating procedures (SOPs) and other quality documentation. Collaborate closely with those assigned to document control duties in specific departments, as applicable. Perform administrative duties to generate documents as necessary, with inputs from subject matter experts. Proof reads all change documents for proper formatting, correct spelling, punctuation and general accuracy. | 4/5/2019 |
| 15707 | Tempus Chicago, IL Jr. Clinical Trials Data Specialist BS or MS in genetics, or related Exp: 0-2 years |
We are looking for a Jr. Clinical Trials Data Analyst who will work with our clinical and computational biology team on reports for clinical and research use. Responsibilities include: Works collaboratively within cross-functional teams at Tempus (including but not limited to scientists, pathologists, product development) to create customized clinical reports. Analyze patient clinical records and molecular testing results to identify potential clinical trials. Perform critical quality control functions in clinical report workflow. Support ongoing and future projects within the team. | 4/5/2019 |
| 15708 | Tempus Chicago, IL Product Designer (Entry Level) BS/BA Exp: 0-3 years of product design for web applications |
As a Product Designer, you will be responsible for defining the experience of our products. You will be supporting and collaborating with the lead designer on this project and future endeavors. Support user-centered design projects with internal and external stakeholders, including physicians. Define and prototype your solutions, iterating quickly with your cross-functional team of engineers, computational biologists, data scientists, and other designers. Manage timelines in an agile environment to deliver enterprise-grade product | 4/5/2019 |
| 15709 | Tempus Chicago, IL Clinical Molecular Technologist - PM Shift BS or MS in medical technologies, chemistry, or biological sciences Exp: 0-2 years |
As a clinical molecular technologist, you will be responsible for: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field | 4/5/2019 |
| 15710 | Tergus Pharma Durham, NC Scientist I, IVRT BS in pharma sciences, chemistry, biology, or related Exp: 1-2 years lab experience |
Responsibilities include: Conducts experiments under limited supervision and maintains excellent notebook documentation in a GMP/GLP lab, Performs In Vitro Release Testing (IVRT) for topical formulations such as Gels, Creams, Ointments, Films and Ophthalmic Solutions as per customer needs. Prepares solutions for IVRT and High Performance Liquid Chromatography (HPLC) analysis such as Mobile Phase and buffer. | 4/5/2019 |
| 15711 | Teva Elizabeth, NJ Quality Analyst I BS/BA in sciences Exp: 1-3 years in QA |
The Quality Analyst I (QA Specialist: Complaint Investigation Support) is responsible for the general oversight of Customer Complaints, Complaint Deviations & CAPAs, and Documentation Change Request/Revision (Protocols, SOPs, Lists, Forms, APR attachments, etc.) associated with departmental procedures. Essential duties include: Receive complaints through the designated software system in a timely manner. In accordance with applicable standard operating procedures (SOPs) categorize the complaint, make appropriate contact with the complainant to obtain information required to properly investigate the complaint and complete the applicable fields in the system to document the activities. Request the return of samples, when required, and determine the necessary actions required to thoroughly investigate the complaint, including but not limited to documenting the information received through interviews with parties impacted by the complaint submission, documenting the information received from submitted documentation and field samples, submitting samples to the Quality Control laboratory for analysis, sending samples out to outside vendors for analysis, requesting information for various departments to support the complaint investigation and coordinating the complaint investigation with impacted departments, including other Actavis sites and contract vendors. | 4/5/2019 |
| 15712 | Teva Salt Lake City, UT Laboratory Tech I HS Diploma Exp: 1+ years in manufacturing lab |
Under close supervision, performs limited or routine testing of raw materials, components and finished products, prepares standard and sample solutions, and maintains appropriate sample testing documentation. Duties include: Learns to perform sampling and in accordance with Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). Learns to conduct routine analysis of raw materials (identification and assay) using Ultra violet/infrared (UV/IR), thin layer chromatography (TLC) and automatic titration. Learns to dispose of acid waste and organic solvent waste according to Environmental Protection Agency (EPA) regulations, and transfers gas cylinders as instructed by management. | 4/5/2019 |
| 15713 | Teva Salt Lake City, UT Quality Control Analyst I BS/BA in sciences Exp: 1+ years lab experience |
Under general supervision, performs cGMP laboratory analyses of Finished products and in process materials. Performs stability testing for Finished products. Performs maintenance and calibration of analytical instruments. Duties include: Operates general analytical instruments during the testing of finished products using HPLC, UPLC, GC-FID, UV-VIS, FTIR, automatic titrators, Dissolution Apparatus, particle size analyzer, Instron, Densitometer, Rheometer, viscometer (LV/RV/Cone and Plate), pH meter and analytical balance. Prepares standard, sample, and buffer solutions as required by test methods and performs all necessary calculations associated. Labels, transcribes and records documentation such as report sheets and laboratory notebooks as required by SOPs. Cleans, maintains and calibrates laboratory equipment to ensure compliance with current Good Manufacturing Procedures (cGMP). | 4/5/2019 |
| 15714 | Teva Salt Lake City, UT QC Planner-Quality Lab Planner BS/BA in chemistry or related Exp: 1+ years in QC Lab |
Responsible for prioritizing and coordinating testing of raw material, in-process, bulk product, packaged finished product, stability samples, micro samples, and/or water samples for analysts, as needed to support manufacturing. Assist in the checking/auditing of raw data and various logs generated by analysts. | 4/5/2019 |
| 15715 | Teva West Chester, PA Biological Researcher I BS or MS in related field Exp: BS: 1-2 years, MS: 0-1 years |
Responsible for Operations fo GLP Fill-Finish manufacturing facility for parental DP's. Perform all activities supporting the production of sterile DP, including but not limited to: operation of the filling line, filter integrity testing, preparation of components and supplies including use of the autoclave, documentation (batch records, logbooks, etc.), routine in-process analytical testing, visual inspection, and cleaning of critical process equipment. Support supply chain logistics to enable early Toxicology and Clinical DP manufacturing including materials movement, change controls, relevant documentation readiness through interface with internal or external CMO sites. | 4/5/2019 |
| 15716 | Teva West Chester, PA Research Associate BS or MS in biology or related Exp: BS: 1-2 years, MS: 0-1 years |
Perform research laboratory tasks and experiments, making detailed observations, and analyzing data under the supervision of a supervisor. Responsible for performance of assays for validation of test methods according to pre-approved validation plans and acceptance criteria and in accordance with relevant method SOPs and most recent regulatory guidelines. Responsible for sample handling and performs sample analysis from pre-clinical or clinical studies in accordance with the approved method SOPs. Maintains laboratory equipment and inventory levels for laboratory supplies. May also write summaries, reports, and protocols regarding experiments. | 4/5/2019 |
| 15717 | Teva Cincinnati, OH Quality Analyst I BS/BA in sciences Exp: 1-3 years in pharma or manufacturing |
Responsible for reviewing documentation for batches that are manufactured and packaged. Assure compliance with cGMP before being released for further processing, packaging or commercial market. Review completed manufacturing and packaging documents, as well as laboratory test specification sheets. Ensure all pertinent information is compiled, reviewed and approved prior to any product disposition. Identifies improvements/new procedures/ compliance gaps based on applicable regulations. Assign QA status (Release/Reject/Quarantine/Impound) to work-in-process and finished product. Investigates and troubleshoots all routine problems which occur during work assignments. | 4/5/2019 |
| 15718 | Solid Biosciences Cambridge, MA Associate Process Engineer, Upstream Manufacturing Science & Technology BS/BA in life sciences, engineering, or related Exp: 0-2 years |
This position will provide engineering support in the upstream process for tech transfers to contract manufacturing organizations as well as technical support for ongoing manufacturing operations through process monitoring, troubleshooting, and process improvements. Key duties include: Support scale-up, process optimization, technology transfer, and start-up activities. Includes onsite presence at our contract manufacturing organizations. Support the development of new processes and technologies to improve yields, product quality, and process robustness. | 4/1/2019 |
| 15719 | Sorrento Therapeutics San Diego, CA Manufacutring Associate BS/BA in biology, biomedical sciences, chemical engineering or related Exp: 0-2 years |
A Manufacturing Associate who will be responsible for manufacturing CAR-T cells per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Responsibilities include: Weigh and measures in-process materials to ensure proper quantities are added/removed. Adheres to the production schedule ensuring on-time, internal production logistics. | 4/1/2019 |
| 15720 | Sorrento Therapeutics San Diego, CA CAR-T Process Development Positions MS in biology or related Exp: 1-2 years |
The individual must have good understanding of primary cell immunology and tumor biology. Previous experience in related areas is preferred but not required. Responsibilities include: Planning and executing human T cell studies focused on optimizing processes for manufacturing CAR-T cells at pilot and GMP scale. Coordinating experiments and projects collaboratively with R&D team and manufacture team. Maintain detailed documentation records and author reports, SOPs, batch records and other materials to facilitate tech transfer, manufacturing and regulatory submissions | 4/1/2019 |
| 15721 | Sorrento Therapeutics San Diego, CA RESEARCH ASSOCIATE, ANALYTICAL DEVELOPMENT BS in analytical chemistry, biochemistry, or related Exp: 0-4 years |
We are seeking a highly motivated individual to join our analytical development and quality control team. The position offers a unique opportunity for the candidate to work on a variety of projects using various techniques to assess analytes. The position’s focus will be on therapeutic protein drugs development with analytical methods development and validation, characterization and release testing of drug substance and drug product, and stability testing in a GMP- and GLP-compliant environment. | 4/1/2019 |
| 15722 | Sotera San Diego, CA Firmware Verification Engineer BS in computer sciences or related Exp: 1+ years software verification |
The Firmware Verification Engineer of Sotera Wireless will develop, implement, perform, and document both automated and manual software verification tests for the company’s proprietary embedded software. The verification engineer will be required to collaborate with all product development teams: embedded software, systems software, hardware, data science, and software quality assurance. | 4/1/2019 |
| 15723 | Spherotech Lake Forest, IL Quality Control Associate BS in chemistry or related Exp: 1+ years |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. This | 4/1/2019 |
| 15724 | Sprint PNS System Cleveland, OH Clinical Research Associate I BS in life sciences Exp: 1-2 years in research |
Primary responsibilities include: Coordinates and implements clinical study activities for product development projects. Works directly with the clinical, research, and regulatory staff to execute clinical studies. Trains clinical site staff on study protocols, good clinical practices and use of investigational devices. Coordinates and monitors clinical studies to ensure compliance with study protocols, regulatory requirements and Good Clinical Practices. | 4/1/2019 |
| 15725 | Springfield Clinic Springfield, IL Patient Access Specialist - Plastic Surgery HS Diploma Exp: 1+ years in medical office |
Under the direct supervision of the Operations Manager, the Patient Access Specialist is responsible for facilitating patient access services by managing incoming calls, assisting clinic customers at first point of contact, and streamlining clinic-wide communications. Also responsible for the daily work schedule for a group of physicians/staff by answering the phones, obtaining records, verifying patient information, scheduling appointments, entering charges and collecting payments. | 4/1/2019 |
| 15726 | Starkey Hearing Technologies Eden Prairie, MN Research Audiologist I MS+ in audiology Exp: 1+ year |
We are looking for a Research Audiologist that will be responsible for research, subject and data management related to activities pertaining to Alpha and Beta product evaluations, pilot testing, and hearing aid fitting methods. This position will assist in determining the direction of product development. Work will be collaborative with other researchers and personnel in Minnesota. | 4/1/2019 |
| 15727 | Starkey Hearing Technologies Eden Prairie, MN Regulatory Affairs Engineer II BS/BA in sciences or engineering Exp: 1+ years |
We are seeking to add a Regulatory Affairs Engineer II that will be responsible for supporting all Regulatory affairs for medical devices and hearing related products. This position will work with various departments across the organization such as Sales and Marketing to the Product Development group with guidance from senior regulatory personnel throughout the product life cycle. You would support activities that keeps Starkey current with changes to medical device regulations. This position is also responsible for creating and maintaining the technical files for all medical devices and hearing related products. | 4/1/2019 |
| 15728 | Stellartech Milpitas, CA R&D Technician HS Diploma or BS in life sciences Exp: 1+ years |
Primary responsibilities include: Provide general technical assistance to engineering and manufacturing operations. Design and develop 3D machined, formed and molded parts in Solidworks or other 3D modeling program. Assemble electromechanical medical devices. Build prototype circuits and enclosures. | 4/1/2019 |
| 15729 | Stellartech Milpitas, CA Quality Engineer II BS Exp: 1-3 years |
Perform quality engineering development activities for new product designs by assisting Engineering in the preparation of design and development plans, Design History File documentation, and Design History File preparation. Review and approve Device Master Record documentation for new product design and maintenance, including: bills of material, assembly procedures, manufacturing operations, assembly diagrams, test procedures, component specifications, labeling, and operator’s manuals. Perform ongoing quality engineering activities on current products to improve product designs and/or manufacturing processes including participation in NCM, Complaint, and CAPA investigations and actions as necessary. Assist in maintenance and improvement of the Quality System with guidance of QA Management, including internal audits, external audits, and quality improvement activities. | 4/1/2019 |
| 15730 | Regis Technologies Chicago, IL PRODUCTION OPERATOR HS Diploma Exp: 0-2 years |
North suburban Chicago contract pharmaceutical manufacturing company needs a Reactor Operator to operate and clean equipment used in the production of bulk chemicals. Responsibilities include: Operation of all plant equipment. Cleaning of all plant equipment. Staging of raw materials in production areas. Unloading of intermediates and products from equipment | 3/31/2019 |
| 15731 | Regis Technologies Chicago, IL PRODUCTION CHEMIST BS/BA in science or engineering Exp: 0-2 years |
North suburban Chicago contract pharmaceutical manufacturing company needs a Production Chemist to operate and clean equipment used in the production of bulk chemicals. Responsibilities include: Operation of all plant equipment. Cleaning of all plant equipment. Interaction with clients and sales team. Directing operators and technician | 3/31/2019 |
| 15732 | Zygo Middlefield, CT Associate Software Engineer BS in computer sciences Exp: Entry Level |
The selected candidate will develop, code, test, and debug new software and enhancements to existing software under the direction of senior developers. Our development approach fosters communication and collaboration across multiple scientific disciplines and provides all members of our team’s opportunities to contribute creatively to our projects. This position supports Zygo’s growing workload in application development for the Metrology and High-Precision Optical Fabrication markets. | 3/31/2019 |
| 15733 | Relay Cambridge, MA Research Associate - Compound Management AS or higher in life sciences Exp: 0-2 years |
You will lead fulfillment of dry and solution-based compound sample requests for scientific teams. Our Compound Management group is highly automated and in this role you can expect to operate laboratory robotics on the reg, while interfacing with web-based software tools. You will also be responsible for processing new samples into the archive inventory, which also includes accurate sample weighing and dissolution. | 3/31/2019 |
| 15734 | REMD Biotherapeutics Camarillo, CA Associate Scientist BS/BA in cell or molecular biology Exp: 0-2 years lab experience |
REMD Biotherapeutics is seeking exceptionally motivated scientists with strong background and proven track records in molecular and cellular biology to join our Drug Discovery team located in Camarillo, CA. Responsibilities in this role include: Design and perform cutting-edge research that utilizes genetic engineering to create novel therapeutic proteins and the cell-based assays needed to assess their biological activity. Work independently and collaboratively to develop and execute novel physical and biological assays required to evaluate new antibody-derived therapeutic proteins. Organize, analyze and present complex data generated on novel proteins in a scientifically rigorous manner for the purpose of advancing clinical candidates. | 3/31/2019 |
| 15735 | Revance Newark, CA QC Analyst I (Contract) BS/BA Exp: 0-2 years lab experience |
Conduct routine and non-routine analysis of in-process and finished products. Perform biochemical and/or chemical analyses of product to ensure stability. Compile data for documentation of test procedures that may include biochemical and chemical assays, initial lot release and stability testing and formulation studies. Revise and update standard operating procedures as needed. May participate in special projects as method validation or method transfer on analytical department. | 3/31/2019 |
| 15736 | Revance Newark, CA Clinical Trial Associate BS/BA in life sciences or related Exp: 0-2 years |
Acts as the primary liaison between Clinical Program Leads and Clinical Research Organizations (CROs). Supports Clinical Program Leads in operational and logistical tasks of pre-start up, start up and start up activities related to clinical trials performed according to regulatory, GCP ICH requirements, operational best practices and quality standards (ICH GCP / country and local requirements / company SOPs). Provide support across the Clinical department and partner with Clinical Program Leads and Medical Affairs on specific tasks involved in support of running clinical trials, from start- up through completion. | 3/31/2019 |
| 15737 | Rheonix Ithaca, NY System Integration Engineer BS in mechanical, systems or biomedical engineering Exp: 0-2 years |
The Systems Integration Engineer is responsible for integrating new biology and engineering developments into the product line and transferring to manufacturing. In this role he/she will work closely with the engineering and biology teams to develop and perform optimization and characterization experiments. He/she will also provide external customer support for system installations, maintenance and repair. | 3/31/2019 |
| 15738 | Rho Chapel Hill, NC Business Development Associate BS/BA Exp: 0-2 years |
The Business Development Associate will support the Business Development team in their efforts to achieve territory and corporate sales goals as well as assist in creating and executing a successful sales strategy. The ideal candidate will be adept at client-specific research and will provide active support in generating business leads. Responsibilities include: Perform outreach (phone, mail, email) to potential leads to generate interest in Rho’s services with provided text and scripts. Schedule telephone, face-to-face, and web meeting appointments for Rho business development professionals. Ensure a high level of communication and customer service | 3/31/2019 |
| 15739 | Purdue Wilson, NC Pharmaceutical Technician HS Diploma Exp: 0-5 years in pharma |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Responsibilities include: Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Prepare raw materials, blends, and bulk accountability throughout manufacturing processes. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. | 3/31/2019 |
| 15740 | Roivant New York, NY Tech Analyst, Roivant Analyst Program BS/BA or MS Exp: 0 years |
The two-year tech rotational program at Roivant begins summer 2019 and will give you experience across a variety of functions within Roivant and our subsidiary companies. Throughout our businesses, analysts will look for ways to integrate modern technology and will have the opportunity to develop Roivant’s innovative health and pharmaceutical companies in their early stages. As an analyst, you will have the opportunity to rotate through the following teams: Digital innovation, Digital Product, Devops, Data Architecture | 3/31/2019 |
| 15741 | Roivant New York, NY Accounting Analyst (Roivant Analyst Program) BS/BA or MS Exp: 0 years |
Roivant offers a two-year analyst program, beginning in summer 2019, with three tracks – general, tech, and accounting. Within the accounting track, analysts will focus on the different functions of our Accounting and Finance teams. In each area, analysts will work side-by-side with experienced professionals and senior management to improve overall department efficiency, company controls, procedures, as well as provide general departmental support. | 3/31/2019 |
| 15742 | Sabbio Therapeutics Sioux Falls, SD Research Associate (VAC) BS/BA in relevant field Exp: 1-5 years lab experience |
We're seeking a Research Associate to perform experiments, immunoassays and other technical procedures in addition to writing research protocol and reporting experimental data. Essential duties: • Conduct routine laboratory procedures, assays, and experiments according to protocols. • Complete training and submit records on established protocols, assays and procedures. • Collect, evaluate, interpret and document research data according to scientific objectives. • Log, store and maintain samples with accurate records for research and production projects. • Maintain laboratory to ensure smooth operation and timely lab activities.We're seeking a Research Associate to perform experiments, immunoassays and other technical procedures in addition to writing research protocol and reporting experimental data. Essential duties: • Conduct routine laboratory procedures, assays, and experiments according to protocols. • Complete training and submit records on established protocols, assays and procedures. • Collect, evaluate, interpret and document research data according to scientific objectives. • Log, store and maintain samples with accurate records for research and production projects. • Maintain laboratory to ensure smooth operation and timely lab activities.We're seeking a Research Associate to perform experiments, immunoassays and other technical procedures in addition to writing research protocol and reporting experimental data. Essential duties: • Conduct routine laboratory procedures, assays, and experiments according to protocols. • Complete training and submit records on established protocols, assays and procedures. • Collect, evaluate, interpret and document research data according to scientific objectives. • Log, store and maintain samples with accurate records for research and production projects. • Maintain laboratory to ensure smooth operation and timely lab activities.We're seeking a Research Associate to perform experiments, immunoassays and other technical procedures in addition to writing research protocol and reporting experimental data. Essential duties: • Conduct routine laboratory procedures, assays, and experiments according to protocols. • Complete training and submit records on established protocols, assays and procedures. • Collect, evaluate, interpret and document research data according to scientific objectives. • Log, store and maintain samples with accurate records for research and production projects. • Maintain laboratory to ensure smo | 3/31/2019 |
| 15743 | Santa Cruz Biotechnologies Paso Robles, CA Research Assistant BS in biology or related Exp: 0-2 years (entry level) |
This is a full time position with career advancement opportunities within the company. Responsibilities include: Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from supervisor. Strong scientific background and business communication skills. | 3/31/2019 |
| 15744 | Sarepta Therapeutics Andover, MS Associate I BS in chemical engineering, process chemistry, or related Exp: 1+ years organic lab experience |
The Associate I, Oligonucleotide Chemistry will work on a rapidly growing team focused on supporting internal Research and Discovery, Analytical Development, Pre-clinical, and Toxicology groups. This role will perform high throughput synthesis, purification, and isolation of Sarepta’s phosphorodiamidate morpholino oligomers (PMOs). The Research Manufacturing Oligonucleotide Chemistry group synthesizes PMOs for lead-candidate screening, Analytical standards, and commercialization support. | 3/31/2019 |
| 15745 | Sarepta Therapeutics Andover, MS Associate I, Nucleoside Manufacturing BS in chemical engineering, process chemistry, or related Exp: 0-1 years |
The Associate I, Nucleoside Manufacturing will focus on support of our Contract Nucleoside Manufacturing sites including oversight of both routine manufacturing and tech transfer of new/improved processes to the sites. Nucleoside manufacturing ensures uninterrupted supply of API and sterile drug product in support of Sarepta’s manufacturing organization. The position is responsible for manufacturing trending, interaction with Sarepta process development, and production planning and execution with contract manufacturing organizations (CMOs). | 3/31/2019 |
| 15746 | Sarepta Therapeutics Columbus , OH Research Support/ Animal Technician HS Diploma Exp: 1-2 years |
Follows standard operating procedures and maintains recordkeeping pertaining to equipment operation, animal and supply inventories in accordance with federal and state guidelines and regulations. Handle, transfer, and distribute mice, supplies and waste as needed to and from work area(s). Coordinate with vendors and supervisors on operational, administrative and technical responsibilities . Monitor the daily health and welfare of the animals according to IACUC guidelines | 3/31/2019 |
| 15747 | Scholar Rock Cambridge, MA Laboratory Operations Assistant HS Diploma or BS in life sciences Exp: 0-1 years |
The Laboratory Operations Assistant will support laboratory scientists in the pursuit of new therapeutics with the potential to change patients’ lives. The candidate will be an essential part of maintaining a highly functional research lab in the biotech industry. Responsibilities include: Assist scientists and facilities team in conducting laboratory support tasks as needed. Stock and control inventory for the research lab. Perform routine maintenance lab maintenance including daily, weekly, monthly and as needed equipment maintenance . | 3/31/2019 |
| 15748 | Scholar Rock Cambridge, MA Associate Scientist / Senior Associate Scientist, Protein Sciences (multiple openings) BS or MS in biology or related Exp: 1-5 years |
Candidate will join the Protein Sciences group to express and manufacture antigens, antibodies, and proteins to support multiple Discovery Programs. Responsibilities include: Purification and characterization of antigens and antibodies to support the Discovery Research team at both small and large scale amounts. Generate and provide protein reagents in a timely manner to colleagues to support Discovery Research. Participate in cross-functional teams as Protein Sciences representative and/or subject matter expert . | 3/31/2019 |
| 15749 | Seattle Genetics Bothell , WA QC Analyst I BS/BA in sciences Exp: 0-3 years |
This position is located within the Quality Control department and is responsible for performing potency/binding assays (cellular bioassays and ELISA) and other related Quality Control methods for release and stability testing. Additional responsibilities include: preparation of solutions for potency assays, perform routine preventative maintenance on lab equipment, lab stocking, and performing cell passages. | 3/31/2019 |
| 15750 | Seattle Genetics Bothell , WA The Analytical Sciences Group at Seattle Genetics is seeking a highly motivated Research Associate with experience in release and characterization met BS/BA in analytical chemistry, biochem, or related Exp: 0-2 years |
The Analytical Sciences Group at Seattle Genetics is seeking a highly motivated Research Associate with experience in release and characterization method development for monoclonal antibodies and antibody drug conjugates. His/her responsibilities will include development and qualification of chromatographic and electrophoretic methods to support process development, quality control and physicochemical characterization of therapeutic antibodies and antibody drug conjugates. The candidate will (1) Conduct experiments to support method development and qualifications for mAbs and ADCs (2) Generate and interpret high quality data and technical reports to support various regulatory submissions including IND, BLA, IMPD, etc., and | 3/31/2019 |
| 15751 | Seattle Genetics Bothell , WA Research Associate I, BioProcess Development BS/BA in chemistry, engineering, biology, or related Exp: 0-2 years |
The BioProcess Development Department at Seattle Genetics is seeking a Research Associate to participate in the purification development efforts to support process development for our antibody and antibody-drug conjugate programs. Responsibilities include: Perform bench-scale chromatography and filtration development and characterization studies. Conduct platform fit assessments for early phase programs. | 3/31/2019 |
| 15752 | Seattle Genetics Bothell , WA Research Associate I, Analytical Sciences - MS Core Group BS in analytical chemistry, biochemistry, or related Exp: 0-2 years |
The Analytical Sciences Group at Seattle Genetics is seeking a highly motivated Research Associate to join the mass spectrometry (MS) core group. The ideal candidate will possess hands-on experience with protein mass spectrometry methods and data analysis. Primary responsibilities will include generation and interpretation of MS-based characterization data for monoclonal antibodies (mAbs) and Antibody drug conjugates (ADCs) in support of clinical and commercial programs. Responsibilities include: Conduct experiments aimed at characterizing posttranslationally modified mAbs and ADCs. Generate and interpret high quality data and technical reports to support various regulatory submissions including IND, BLA, IMPD, etc.. | 3/31/2019 |
| 15753 | Seattle Genetics Bothell , WA Shipping & Receiving Associate I HS Diploma or AS or BS Exp: 0-2 years in shipping/receiving |
Responsible for receipt, storage, and delivery of laboratory supplies & equipment, office supplies and other products such as break room supplies. Shipping & Receiving Associates I must demonstrate meticulous attention to detail, flexibility and a willingness to perform a wide variety of tasks while adhering to defined procedures. The position will work directly with the Purchasing, Research & Development, and Finance departments to accurately track, record, deliver and maintain the correct amount of supplies and equipment to the correct locations at all times. | 3/31/2019 |
| 15754 | Sebela Rosewell, GA QC Chemist BS in chemistry or related Exp: 0-2 years in cGMP environment |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. Principle duties include: Perform testing of raw materials and products. Perform instrument qualification and maintenance. Perform test method validation/verification. Review analytical data for completeness, accuracy, and compliance | 3/31/2019 |
| 15755 | Sedia Biosciences Portland, OR QC TECHNICIAN AS in technical field Exp: 1+ years lab experience |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. Demonstrates a high level of independent judgment and discretion in the timely identification, investigation and resolution of events impacting the Quality of products and processes. | 3/31/2019 |
| 15756 | Sedia Biosciences Portland, OR MANUFACTURING TECHNICIAN AS in technical field Exp: 1+ years lab experience |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. The Manufacturing Technician will adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance. | 3/31/2019 |
| 15757 | Sedia Biosciences Portland, OR Associate/Assistant Protein Scientist (R&D) BS in biochemistry, biology, or related Exp: 1-3 years |
The ideal candidate will assist in the development, expression, and scale up recombinant proteins from bacterial or other vectors, purify proteins and perform subsequent validation and quality assessments. The selected candidate will have demonstrated experience in most of the technical skillsets and be able to work in a small group of individuals, in a highly cross-functional environment. | 3/31/2019 |
| 15758 | Sedia Biosciences Portland, OR SCIENTIST/ASSOCIATE SCIENTIST (R&D-Product Development) MS in biology, chemistry or related Exp: 1-3 years lab experience |
This position would be a full-time exempt position (40 hours per week) at our primary laboratory facility in Northeast Portland. The successful candidate will be responsible for running laboratory tests, recording data, performing some degree of data analysis, drafting protocols, and communicating with managers from R&D and other departments. They will also be asked to participate in production of prototype products, and assist in transition of those procedures (through training and/or record-keeping) to our manufacturing department. Workflow is approximately 50-70% laboratory work, with the remainder being office work. The nature of our work requires the candidate to be capable of working comfortably in a BSL 2 laboratory | 3/31/2019 |
| 15759 | Sekisui Charlottetown, CA Research Associate BS in science or technical discipline Exp: 0-2 years |
The Research Associate will be responsible for designing, executing and interpreting experiments and analytical procedures under general supervision. Initiates, directs and executes pre-clinical scientific research and/or development strategies in research and/or development. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems. Plans and executes laboratory research. Maintains broad knowledge of state-of-the-art principles and theories. May participate in development of patent applications. Interfaces with various departments. | 3/31/2019 |
| 15760 | LabCorp Birmingham, AL Histotechnologist AS degree Exp: 1-3 years in histology |
Performs all technical duties related to the production of histo-pathological slides including embedding, microtomy, special stains, and IHC staining. 2nd shift. | 3/31/2019 |
| 15761 | LabCorp Burlington, NC Specimen Processing Specialist (Microbiology) HS Diploma Exp: 1-3 years in clinical lab |
This is a multi-discipline position with 3 primary components: specimen accessioning, sample splitting/sorting and data entry. Prepares laboratory specimens for designated departments/locations prior to laboratory analysis and testing and routes specimens by type to various staging areas. Performs all paperwork, technical and non-technical procedures required to process and submit specimens. Assigns specific computer generated identification numbers, checks for accuracy and records all items processed. Operates data entry terminals and automated data systems, follows standard sequences/coding when entering data and corrects, edits, and/or verifies data entered into automated systems. Must be able to perform eSIS audits to resolve any outstanding problems. 3rd shift | 3/31/2019 |
| 15762 | LabCorp Rapid City, SD Lab Technician AS in medical lab technology Exp: 1-3 years |
Performs a variety of laboratory tests and assays in accordance with established policies, procedures and regulations in a designated technical department. nterprets results, subject to verification by Technologist/Supervisor, and providing allowance by State regulations. | 3/31/2019 |
| 15763 | LabCorp Tustin, CA Medical Data Entry/Accessioning HS Diploma Exp: 1-2 years |
Prepares laboratory specimens for designated departments/locations prior to laboratory analysis and testing. Unpacks specimens from branches or ports and routes specimens by type to various staging areas. Prepares all specimens received for testing in designated laboratory departments or locations such as staging of specimens, centrifuge, separate serum, and blood smears. Aliquots sample for departments. Prepares excess specimen samples for storage and resolves and document problem specimens. 2nd shift | 3/31/2019 |
| 15764 | LabCorp Seattle, WA Phlebotomist HS Diploma w/ WA Medical Assistant Phlebotomy cert Exp: 1+ years |
PST meets minimum requirements and experience for client office and roving (with limited locations) positions, and patient service centers offering minimal services. Skill and comprehension level required for this category: Phlebotomy certification (where required) from an accredited agency, completion of an approved phlebotomy training course, or a minimum of one year verifiable phlebotomy experience. Exhibit proficiency in blood collection by venipuncture and capillary technique from patients of all age groups, and urine drug screen collections. Able to grasp a firm understanding of the importance of compliance and safety as outlined during new hire orientation and annual training. | 3/31/2019 |
| 15765 | LabCorp Phoenix, AZ Lab Assistant HS Diploma Exp: 1-2 years |
Performs all paperwork, technical, and non-technical procedures required to process and submit specimens. Assigns specific computer generated identification numbers, checks for accuracy, and records all items processed. Forwards accessioned specimens to designated laboratory location(s); and locating and correcting any discrepancies. Learns and keeps familiar with lab procedures and location of stored specimens. Locates specimens and pulls from various departments as requested. | 3/31/2019 |
| 15766 | SeraCare Milford, MA Research Associate II MS in biochemistry or biology Exp: 0-1 years |
Support includes independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material. Perform general molecular techniques such as plasmid purification, gel-electrophoresis, RNA transcription, and bacterial culturing. Perform nucleic acid analysis (RNA/DNA integrity analysis, real time qPCR, digital PCR) and analyze results. Work with supervisor to plan and execute new projects as assigned according to the timelines and ensure documentation meets GLP/GMP requirements. | 3/31/2019 |
| 15767 | Merck KGaA St. Louis, MO Technical Service Scientist BS/BA Exp: 1+ years |
The candidate will be a key member of an entry level, interactive technical service team that acts as the front line of communications between customers and our technical service specialists. This team is focused on providing best-in-class customer support via telephone, email and internet. The candidate is responsible for fielding basic technical inquiries on MilliporeSigma's products and navigating more advanced technical inquiries to the appropriate specialist within the organization. Our customer base includes Pharmaceutical and Biotech companies, Universities, Hospitals and Government agencies. Professional communication and schedule flexibility are imperative. | 3/31/2019 |
| 15768 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, chemical enginering or related Exp: 0-4 years |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Shift: Wednesday - Saturday, 4:00 pm - 2-20 am. Job functions include: Safely perform operations to meet quality expectations. Ensure quality throughout the process. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). | 3/31/2019 |
| 15769 | Merck KGaA Rocklin, CA Production Associate HS Diploma Exp: 1+ years |
Under close supervision, the Production Associate participates in entry-level production duties such as filling, labeling, packaging, shipping and other duties as assigned in a laboratory/manufacturing environment. Essential duties include: filling, labeling, packaging, etc. | 3/31/2019 |
| 15770 | Merck KGaA Milwaukee, WI Associate Production Scientist- Flow BS/BA in chemistry , biology or related Exp: 0-4 years |
While working 2nd shift (3:30 pm to 12:00am), continuously manufacture products according to established flow protocols, provide technical support to others and perform operations in support of the group and department. Essential job duties include: Safely perform operations to meet quality expectations. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. Participate in process improvements under the guidance of a Supervisor or Scientist. | 3/31/2019 |
| 15771 | Merck KGaA Billerica, MA QC Research Associate - Protein Science BS/BA in biology or related Exp: 1+ years lab experience |
The Protein Science / Buffer-media prep and QC group is a core function of the Protein and Cell Sciences (PCS) department that supports both early and late stage discovery projects and seeking a QC Research Associate. Responsible for small to large scale media and buffer production, as well as QC analytics supporting GLP tox drug substance production. Responsible for media / buffer preparation, equipment maintenance and calibration, data analysis, electronic lab notebook and batch record documentation. Responsible for media and buffer preparation to meet GLP tox protein production and reference run schedules, which includes raw material and chemical procurement and inventory control. | 3/31/2019 |
| 15772 | Sinclair Research Auxvasse, MO Formulations Technician MS in chemistry Exp: 0-2 years |
You will set up and manage the analytical laboratory and instrumentation including being responsible for SOP development, analytical software validation, dose formulation preparation, dose analysis and reporting in compliance with relevant regulations including GLP. Additionally, you may monitor analytical equipment performance and perform required routine maintenance procedures. As the member of the Lab Team at a Pre-Clinical CRO, it is also important to ensure we closely monitor laboratory supplies and cleanliness to provide a clean and regulatory compliant laboratory. | 3/31/2019 |
| 15773 | Singota Solutions Bloomington, IN Associate Quality Control Analyst BS in chemistry or related Exp: 1+ years |
Supportthe Quality Control function with respect to raw material, in-process, release and stability testing. Collaboratively participates in Development functionsfor the company including pre-formulation, formulation, process and analytical development activities. Specifically: Operate various lab instruments and equipment including (but not limited to): Karl Fisher, pH, HPLC, FTIR, UV-VIS, DSC, TOC, Lab-ware washers, Autoclave, Laminar Flow Hoods, Bio-Hazard Hood, Microbalances, and other diverse lab equipment and various wet chemistry techniques. Perform quality control analyses on a variety of equipment following formal written documentation, including SOPs, client methods, and compendialrequirements | 3/31/2019 |
| 15774 | Siolta Therapeutics San Francisco, CA Research Technician – Microbiology MS in microbiology or related Exp: 0-2 years |
Siolta Therapeutics is seeking a highly motivated and talented technical staff scientist to provide support for the company’s therapeutic development program focused on prevention/treatment of airway inflammation through manipulation of the gut microbiome. The successful candidate will work closely with other team members on preclinical studies of a rationally designed microbial therapeutic. The successful candidate will be technically proficient in microbial culture and molecular techniques. | 3/31/2019 |
| 15775 | Smith&Nephew Andover, MA Test Engineer I BS or equivalent Exp: 0-2 years |
Role is a Test Engineer, an individual contributor responsible for development and design of test fixtures, software and verification and feasibility testing as it relates to R&D development activities for capital devices. Follow FDA guidelines for Design Controls and internal quality processes. Interact with suppliers to ensure proper process controls on the parts we design into our products. Work cross functionally with marketing, quality, manufacturing and sustainability to ensure the customer experience is the best we can make it. | 3/31/2019 |
| 15776 | Smith&Nephew Mansfield, MA Quality Engineer 1 BS in engineering Exp: 0-3 years |
Position functions include: Develops and works with area teams to implement continuous quality improvement programs/productivity projects which may include: vendor certification for ship to stock; design of experiments to identify and thus control process variables; evaluation of lot inspection and initiation of process audit activities; and installation of statistical and non-statistical process controls; simplification of forms. Lead the review, disposition, and corrective action activities associated with discrepant components, materials, sub-assemblies and finished products. Develops and administers an inspection, test, and/or audit program to assure that incoming, in-process, and finished product meets functional specifications and quality standards. | 3/31/2019 |
| 15777 | Profusa South San Francisco, CA Electrical Engineer MS in electrical or computer engineering Exp: 0-5 years |
We seek an experienced electrical engineer with digital/analog circuit design skills to lead the electrical design of these devices. Major responsibilities include: Develop breadboard systems for testing feasibility of optical detection concepts. building miniaturized PCB’s from broad user requirements following design control by gathering and writing engineering requirements, designing the circuit, laying out the PCB, overseeing its fabrication and assembly, powering up and testing the circuit with embedded developer’s help. Interface with vendors to oversee design transfer and manufacturing scale-up. Test electrical functionality of devices | 3/17/2019 |
| 15778 | Progenra Malvern , PA Scientist, Medicinal Chemistry BS or MS in organic/medicinal chemistry Exp: 0-10 years |
As a medicinal chemist you will apply state of the art synthetic chemistry, structural and computational approaches to discover and synthesize novel medicines for a variety of diseases including immuno-oncology, inflammation and neurodegenerative diseases. Research Scientist will independently plan and implement efficient synthetic routes for target compounds and apply state of the art purification and characterization techniques, conduct research with the drug discovery team to develop SAR, analyze the data and write laboratory reports. Position provides opportunities to grow, write papers and patents, and present data at internal, national and international meetings. | 3/17/2019 |
| 15779 | Progenra Malvern , PA Research Associates BS or MS in life sciences Exp: 1-10 years |
Research associates will be expected to apply focused expertise to projects supporting the development of screening assays, and to the discovery and evaluation of compounds active in the various screens. Candidates should have demonstrated proficiency in molecular biology or biochemistry and be willing to contribute to the company product and intellectual property development as exemplified by scientific articles, patents, and internal publications. Research associates are, in addition, expected to present their data in company settings and, if appropriate, at external meetings and in the literature. | 3/17/2019 |
| 15780 | Mission Pharmacal Boerne, TX Compounding Technician HS Diploma Exp: 1+ years |
Responsibilities as a compounding technician include: Mixing chemicals/ingredients and operating all mixing related equipment in a way that meets safety, quality/compliance and productivity objectives. Following and enforcing safety rules, regulations and procedures. Checking all raw materials against MBR ingredients list, recognizes errors and notifies lead personnel as required. Compound/blend all routine formulations and follow MBR as written. | 3/17/2019 |
| 15781 | Protein Simple San Jose, CA Research Associate BS in biochemistry, chemistry, or related Exp: 1-3 years |
The Research Associate will be an integral member developing new technologies for protein analysis. This will position will report in to the R&D Science group and support product development (Consumables/Reagents and Instruments) from conceptualization to commercialization. Key responsibilities include: Assist product development by performing experiments and in-depth data analysis. Design and execute experimental plans independently. Observe and meticulously record all details during product development | 3/17/2019 |
| 15782 | ProTrials Research San Jose, CA Clinical Trials Associate RN or Bachelor Exp: 0-2 years |
Essential duties include: Obtains, reviews, processes, and tracks study related documents (CVs, FDA 1572s, lab certifications, IRB approvals, contracts, protocols, etc.). Maintains and disseminates basic study tracking information including, but not limited to: Visit Reports, Regulatory Documents, Site Contact Lists, Team Contact Lists, Vendor Lists, and Budget Disbursements. Manages and tracks Investigational Product supplies for study centers; receives and prepares requests, ships and returns Investigational Product supplies. | 3/17/2019 |
| 15783 | PSC Biotech Pomona, CA Entry Level CSV Engineer BS in chemical or biomedical engineering Exp: Entry Level |
We are looking for an Entry-Level Computer System Validation Engineer to support our PSC Software Team in Pomona, CA. Job responsibilities include: Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards.Collaborate with project stakeholders and the information systems team to define needs and achievable solutions and/or justifications to system requirements. Initiate/update GxP and Risk Assessments on system. | 3/17/2019 |
| 15784 | Pulmatrix Lexington, MA Engineering Associate BS/BA or MS in chemical, biomedical engineering Exp: 1-5 years in biotech/pharma R&D |
We are seeking a highly motivated engineer to join the Pharmaceutical Development group supporting process development for respiratory drug products. Responsibilities include: Support development and optimization of engineered particle inhaled dosage forms. Specific methods may include bench and pilot-scale spray drying. Perform physicochemical property and aerosol performance characterization of solid-based inhalation dosage forms. | 3/17/2019 |
| 15785 | Purdue Wilson, NC Pharmaceutical Technician HS Diploma Exp: 1-5 years |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Primary responsibilities include: Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing and/or packaging equipment (oral solid dose manufacturing and packaging may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.). Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.). | 3/17/2019 |
| 15786 | Purdue Coventry, RI Lab Technician BS in chemistr Exp: 1-2 years in cGMP,FDA, DEA environments |
This position will also be responsible for providing escort for equipment qualification with vendors, witnessing controlled substance receiving and dispensing, coordinating laboratory waste disposal and pickup, as well as performing and/or facilitating equipment calibrations. This role may perform other related assignments and duties as required. This position will primarily provide hands on support in manufacturing finished product dosage forms – tablets, capsules, liquids and semi-solids. This position will be responsible for equipment set up, product manufacturing and cleaning as per EHS, DEA and FDA regulations. In addition to assisting the product development scientists in manufacturing finished product prototypes, general support of the laboratory is required. Support activities will include managing inventories for raw materials, personal protection equipment, supplies, etc. | 3/17/2019 |
| 15787 | Purdue Coventry, RI Associate Scientist BS/BA or MS in chemistry or related Exp: 1+ years |
The position responsibilities will include both routine and non-routine stability analysis in accordance with cGMP guidelines. These responsibilities will consist of, but are not be limited to, coordinating stability programs, writing stability protocols, SOPs, test methods and final reports. Additional responsibilities include ensuring all laboratory equipment and instrumentation are maintained in compliant condition, to assist in coordinating equipment qualifications, reviewing notebooks/experimental data, trouble shooting and training junior staff. | 3/17/2019 |
| 15788 | Purdue Coventry, RI Process Engineer BS/BA in chemical engineering or chemistry Exp: 1-2 years in manufacturing or engineering |
The Shift Process Engineer performs all manufacturing tasks required for the safe production of active pharmaceutical ingredients in compliance with FDA, DEA, OSHA, Federal, State, and Local regulations. The primary objective of this position is to ensure that all manufacturing operations are conducted in a safe manner with a high regard for all applicable cGMP’s and DEA requirements. Working flexibility across a broad range of chemical operations and participation on self-managed work teams is required. Training for and participation on Emergency Response Team is required. Availability for overtime and shift work (including rotating shifts and seven-day operation) is also required. | 3/17/2019 |
| 15789 | Qiagen Waltham, MD Contract Data Analyst Associate BS/BA in biomedical, electrial, or computer engineering Exp: 1-3 years |
QIAGEN is seeking candidates who will assist in the analysis and interpretation of experimental data generated during the development of the GeneReader sequencer, QIAGEN’s next generation massively parallel DNA sequencing platform (NGS). The successful candidate will play a key role within the GeneReader development team by providing data reduction, interpretation, and visualization of NGS data and associated platform metadata to drive hypothesis-driven research. Data processing and interpretation will be performed using a combination of existing research and development tools and new software development to enhance existing capabilities as needed to support the team. | 3/17/2019 |
| 15790 | Qiagen Waltham, MD Contract Research Associate BS/BA in engineering or sciences Exp: 1+ years |
QIAGEN is seeking candidates who will assist in the development, implementation and optimization of sequencing protocols on the sequencer, QIAGEN’s next generation massively parallel DNA sequencing platform. The successful candidate will be an integral part of the sequencing development team and will be responsible for maintenance and operation of instruments, preparation of reagents according to SOPs as well as executing complex laboratory experiments. | 3/17/2019 |
| 15791 | Qiagen Waltham, MD Associate Bioinformatics Engineer BS in bioinformatics with computer science minor OR MS in bioinformatics Exp: 0-2 years |
You would be working in our clinical implementation team and participate in different projects related to implementation and integration of our QCI Interpret product lines. Responsibilities include: Data engineering supporting QCI Interpret and IVA customers with their bioinformatics data needs. QCI Interpret onboarding including test product, API and report configuration. Participate in other bioinformatics projects within the R&D and Service organization. | 3/17/2019 |
| 15792 | Qiagen Germantown, MD Technical Associate - Kit Assembly Operations HS Diploma Exp: 1-3 years |
The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. Responsible for Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. | 3/17/2019 |
| 15793 | Qiagen Germantown, MD Technical Associate HS Diploma Exp: 1-4 years |
Responsible for the vialing of bulk material, capping, labeling, plate coating and the assembly of kits in compliance with QSR, ISO, OSHA, IVDD, MDD regulations and relevant Standard Operating Procedures. Manual Vialing and coating of components under general supervision as well as using automation (large and small scale) in the production of finished product. Participate in the initiation/change of Quality documentation (i.e. MMRs, SOPs, NRs Variances) as well as ERP (Routers, BOMs, labor and production sheets) related documentation. Employees will be expected to contribute to process improvement initiatives, maintain departmental SOPs and Bluelines and maintain inventory of lab supplies. | 3/17/2019 |
| 15794 | QPS LLC Newark, DE Associate Scientist I - Protein Binding BS/BA in chemistry, analytical chemistry or biochemistry Exp: 0-2 years |
Whether their focus is on small molecules, proteins, antibodies, vaccines or oligonucleotides, QPS provides our clients with a full range of services to support the entire spectrum from early discovery, to IND-enabling ADME, to clinical studies. An Associate Scientist in our DMPK department will be a fully-supervised trainee, responsible for formulations, and sample processing and analysis to support preclinical drug discovery and development. | 3/17/2019 |
| 15795 | QPS LLC Newark, DE Associate Scientist I - Biotransformation BS/BA in chemistry, analytical chemistry or biochemistry Exp: 0-2 years |
An Associate Scientist in our DMPK department will be a fully-supervised trainee, responsible for formulations, and sample processing and analysis to support preclinical drug discovery and development. Responsibilities include: Assist with quantitative and qualitative bio-analytical studies by conducting sample preparation with various analytical chemistry methodologies. Perform routine lab operations, such as sample extraction, preparing reagents, pipette, weigh, monitor, record, label tubes, order and maintain inventory of supplies, and timely disposal of study samples, in a neat/clean manner. | 3/17/2019 |
| 15796 | Bio-Techne Minneapolis, MN Production Assistant 1 HS Diploma Exp: 0-2 years lab experience |
As a Production Assistant 1, you will be responsible for the processing of raw biological material for use in product manufacturing. You will also perform maintenance and cleaning of production equipment and containers to ensure safety and compliance, as well as completing required paperwork. | 3/17/2019 |
| 15797 | Bio-Techne Minneapolis, MN Research Associate BS/BA in biological sciences Exp: 0-2 years lab experience |
As a Research Associate, you will assist in production of insect-derived RUO and GMP recombinant proteins in various bioreactor systems as well as various human cell lines for CAP Survey, media and supplement preparation, and all other duties as assigned. In this position, your scheduled work-week is Tuesday through Saturday. | 3/17/2019 |
| 15798 | Bio-Techne Newark, CA Associate Scientist BS/BA or MS in biology or chemistry Exp: 1-2 years |
Key responsibilities include: Perform manual and automated RNAscope assays to evaluate client-provided tissue samples. Perform digital slide scanning, imaging, and fluorescent microscopy to acquire data. Generate and create custom reports to deliver to clients. Participate in editing custom reports from other projects. | 3/17/2019 |
| 15799 | Reata Pharmaceuticals Irving, TX Research Associate BS or MS in biological sciences Exp: 1-3 years lab experience |
The Research Associate is an entry-level position that is responsible for the execution and analysis of cell-based, molecular biology, and biochemical assays in support of Reata’s drug discovery and development programs. The ideal candidate will be a dynamic member of the research team who can reliably generate data using validated assays. The Research Associate is expected to work both independently and in collaboration with team members. In addition, the Research Associate must thrive in an environment that demands frequent reprioritization of projects and goals. Key responsibilities include: Execute cell and molecular biology experiments to support drug discovery and development. | 3/17/2019 |
| 15800 | RB Hillsborough, NJ Packaging Operator HS Diploma Exp: 1+ year in manufacturing environment |
The Packaging Operator is responsible for providing the Technical and Operational Skills needed to deliver world class results in the key areas of Line Efficiencies, Quality, and Cost while meeting our high standards of Safety, Customer Service, and Teamwork. Key responsibilities include: Operation of Packaging Line and related equipment including startup, clearing jams, manual operations and shutdown. Follows all applicable waste, scrap reduction and recycling guidelines. Assists in changeovers, wash outs and preventative maintenance. | 3/17/2019 |
| 15801 | Recro Gainesville, FL Manufacturing Associate I - 1st/2nd Shift HS Diploma Exp: 6 months |
The Manufacturing Associate I is responsible for the processing of commercial products at the Gainesville Site. This includes receiving order instructions (Batch Records), weighing and staging of materials, solution preparation, solution application (coating beads), drying, screening, machine set-up, sampling, packaging, and storing of the products. | 3/17/2019 |
| 15802 | RefleXion Hayward, CA Firmware Engineer MS in electrical or computer engineering Exp: 1+ years |
This position has responsibility and authority for delivering top quality firmware solution required to meet overall radiotherapy product requirements. This includes: Prototype, design, implement, test, debug and maintain firmware (device drivers, BSPs and Hardware Abstraction Layer library) that serve as the bridge between hardware resources and application software. Participate in completing test cases, conduct embedded systems verification and generating test reports to support a 510(k) submission and FDA clearance. Participate in cross-functional project teams with scientists, technical support and other engineers to resolve software issues. | 3/17/2019 |
| 15803 | Regeneron Tarrytown, NY R&D Associate, Inflammation & Immunology BS/BA Exp: 1-4 years |
Seeking a motivated Research Associate with at least 1-4 years of experience working on inflammation, asthma allergy, autoimmunity or mouse models of human disease to join a highly interactive immunology team. Conducts experiments, predominantly of basic immunology and basic lab techniques. Troubleshoots methodological and technical issues, interprets experimental data and literature, and communicates results to supervisor, department, or project team. Helps create a safe, effective, and efficient working environment. | 3/17/2019 |
| 15804 | Regeneron Tarrytown, NY R&D Associate, Infectious Diseases MS Exp: 0-4 years in lab |
Regeneron is seeking a highly qualified candidate for a R&D Associate for infectious disease target discovery, assay development and monoclonal antibody evaluation and selection. Responsibilities include: Design, execute and control experiments based on protocols. Perform advanced laboratory calculations and manipulations along with the analysis and interpretation of data with little to no supervision. Communicates experimental results, conclusions and ideas directly to supervisor, project team members and management in quality presentation form. Develop new methods or technologies and troubleshoot protocols. | 3/17/2019 |
| 15805 | Regeneron Tarrytown, NY R&D Associate (Non-Clinical Bioanalysis) BS/BA Exp: 0-2 years |
This is an entry level associate position. R&D Associates at this level are required to closely follow instructions regarding the execution of experiments. They are expected to have a basic understanding of general laboratory techniques, such as pipetting and making solutions, in addition to limited experience performing immunoassays. All work is conducted under direct supervision. The associate has minimal decision making capability and requires direct supervision on work assigned. Possesses a knowledge of the basic principles of ELISA obtained through academic training or relevant industry experience. | 3/17/2019 |
| 15806 | Regeneron Tarrytown, NY R&D Associate (Formulation Process Development) BS or MS in biomedical or chemical engineering Exp: 0-3 years |
R&D Associate in the Formulation Development Group (FDG) will work in a state-of-the-art drug product (DP) laboratory developing processes and unit operations for protein-based drug products. The Associate will work closely with FDG leads/scientists to support development activities across multiple programs and will ensure a seamless technology transfer to the manufacturing team. The Associate will also support full functionality of DP process laboratory including setup and maintenance, procurement of tools, as well as equipment installation and operation. Additionally, the position will independently execute process development and analytical characterization studies, and will document the same in electronic notebooks and reports. | 3/17/2019 |
| 15807 | Precision Medicine Group New York, NY Scientific Associate - Medical Writer MS in life sciences Exp: 1-2 years in medical communications |
Scientific Associates develop and write medical content for assigned client account(s) and work in conjunction with all internal teams to ensure that the client vision is achieved and content is medically accurate. Responsibilities include: Developing and writing medical content for multiple and wide-ranging therapeutic areas and appropriate audiences. Ensuring project quality and outcomes by demonstrating in‑depth technical expertise of assigned therapeutic category and/or managed care areas. Developing strategic content for full range of medical content (slide presentations, advisory boards, strategy guides, monographs, discussion guides, training resources, etc.) | 3/15/2019 |
| 15808 | Precision Medicine Group Houston, TX Flow Cytometry Technologist BS/BA in life sciences or related Exp: 0-1 years in flow cytometry |
Day to day tasks as a technologist include: Performing simple and complex processing of blood and body fluids (routine and non-routine procedures). Setting up instrumentation and running calibration samples. Running quality control samples, clinical samples and generating data. Work with QA to perform good documentation and ensure the lab is operating under CLIA, GLP and GCP standards. | 3/15/2019 |
| 15809 | Pfizer Morrisville, NC Associate Scientist, Analytical R&D BS in biology, chemistry or related Exp: 0-2 years |
The qualified individual will be responsible for becoming proficient in a breadth of analytical methodologies including real-time PCR, HPLC, cell-based assays, and other relevant biochemical analysis methods. The colleague must be able to interact effectively with peers and leaders as part of a multi-disciplinary team. The candidate must thrive in a fast-paced, matrixed environment. Attention to detail, strong organizational skills, and effective interpersonal and communication skills are required. Ability to document analytical results in regulated systems and technical reports is also required. | 3/14/2019 |
| 15810 | Pfizer Collegeville, PA Stistical Programmer (Associate) BS or MS in statistics, biological sciences, or related Exp: 1+ years SAS programing |
This role is a hands on statistical programmer supporting study and asset teams in the delivery of less complex statistical programming deliverables. Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures, and qc work for which they are responsible. Ensures adherence to high quality programming standards in their daily work. Accountable for their assigned work in the programming space supporting the programming leads for a particular study or asset deliverable. | 3/14/2019 |
| 15811 | Pharmacyclics Sunnyvale, CA Clinical Project Assistant BS/BA in science, RN or related Exp: 1+ years in pharma, biotech or healthcare setting |
The Clinical Project Assistant (CPA) provides support to the clinical study teams in the execution of clinical trials. Under the direction of the Clinical Project Associate, CTM or Study Lead, the CPA’s primary responsibilities include maintaining Trial Master File (TMF) and Clinical Trial Management System (CTMS) in an inspection-ready state, assisting with site management, initiating collection of and reviewing and tracking essential documents throughout the life of the trial. This role contributes to the production and distribution of study materials and site/study communications. | 3/14/2019 |
| 15812 | Pharm-Olam Raleigh , NC SAS Programmer BS in related field Exp: 1-3 years in research |
To help design analysis data set specifications. Manage and manipulate multiple large SAS data sets, including defining populations and variables, performing calculations and summarizations. Prepare specific analytic deliverables, combining multiple programming outputs to create cohesive reports. Key responsibilities include: Responsible for creating specifications for generation of analysis datasets per ADaM/Pharm-Olam/Sponsor requirements, or as mentioned in SAP. Responsible for writing programming in order to generate tables and listings for clinical data on assigned projects for Production/Validation as assigned by Line Manager. Responsible for assisting in the development of programming procedures for the department. | 3/14/2019 |
| 15813 | Pharm-Olam Houston, TX SAS Programmer BS in related field Exp: 1-3 years in research |
To help design analysis data set specifications. Manage and manipulate multiple large SAS data sets, including defining populations and variables, performing calculations and summarizations. Prepare specific analytic deliverables, combining multiple programming outputs to create cohesive reports. Key responsibilities include: Responsible for creating specifications for generation of analysis datasets per ADaM/Pharm-Olam/Sponsor requirements, or as mentioned in SAP. Ensure SAS programs adhere to specifications/Mock Shells and Pharm-Olam programming standards. Responsible for writing programming in order to generate tables and listings for clinical data on assigned projects for Production/Validation as assigned by Line Manager. | 3/14/2019 |
| 15814 | Stryker Redmond, WA Associate Customer Quality Engineer BS in engineering Exp: 1+ years |
Responsible for continuous product and process quality improvements. Conducts investigations into NCs and CAPAs stemming from the products in the field. Leads root cause activities and Identifies potential failure modes and risks and resolves customer issues appropriately. Knows and applies the fundamental concepts, practices, and procedures of the general Quality and Regulatory post-market environment. Responsibilities include: Gather and analyze Post Market trending data (e.g. Q, service reports, complaints, MDR/MDV) to identify opportunities for quality improvements. Communicate with Customers, members of Field Service and Sales organizations to gather information necessary to carry out investigations. | 3/14/2019 |
| 15815 | PMI Biopharma Solutions Nashville, TN Analytical Chemist, Analytical Development BS in biology, chemistry or related Exp: 1-2 years in pharma |
The Analytical Chemist III position, reporting to the Director, Analytical Development, will operate under moderate supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development. | 3/14/2019 |
| 15816 | PolarityTE Salt Lake City, UT Research Trials Assistant BS in science or technical discipline Exp: 1+ years in clinical research |
PolarityTE is seeking a motivated, responsible, and self-sufficient individual to help support the everyday tasks of the Clinical Trials department. Responsibilities will span multiple trials and indications. Key responsibilities include: Manage the organization of trial files and critical documents. Support clinical trials team with shipments, equipment tracking and management, and supply inventory. Maintain clinical trial metrics and patient enrollment activities for weekly and monthly meetings. etc. | 3/14/2019 |
| 15817 | PolyPeptide Laboratories Group San Diego, CA Production Chemist I BS/BA in chemistry or related Exp: 1-3 years in chromatographic purification |
Job duties include: Responsible for the synthesis and purification of peptides under Good Manufacturing Practices (cGMP). Participates in the development and scale-up of synthesis and purification processes. | 3/14/2019 |
| 15818 | Poseida Therapeutics San Diego, CA Process Development Associate MS in biology Exp: 1+ years |
The Development Associate will be a key member of a dynamic team that develops and implements characterization strategies to support and enable process and clinical development of gene-engineered cell products. This is a lab-based position that will involve hands-on development of clinical manufacturing processes for selecting, gene-modifying and growing T cell subsets. This position will interface with our Research and Development team as well as with outside Contract Manufacturing Organizations. The ideal candidate will be skilled in T cell culture techniques, flow cytometry and have experience working in or supporting cGMP manufacturing projects. The candidate will have good oral and written communication skills, and will work with minimal supervision to design experiments, manage projects, collect data, and prepare reports. | 3/14/2019 |
| 15819 | PPD Middleton, WI Associate QC Reviewer BS in related field Exp: 0-2 years |
As associate QC reviewer you will be responsible for: Ensures the quality of laboratory data and reports. Reviews chromatographic data and related notebooks as specified by Standard Operating Procedures (SOPs). Evaluates data to ensure compliance with analytical methods, client criteria, Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) | 3/14/2019 |
| 15820 | PPD Middleton, WI Assoc Scientist BS in related field Exp: 1+ years |
Responsibilities include: Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/14/2019 |
| 15821 | PPD Richmond, VA Associate / QA Auditor I - Vaccines BS/BA in life science or related Exp: 1+ years in clinical research |
Responsibilities include: Audits laboratory data for compliance with methods and standard operating procedures and report findings. Audits sample result tables and analytical reports for completeness and accurate representation of the data and report findings. Assists in the preparation of audit findings and/or other related information. Serves as a resource to operational departments on audit or quality assurance subject matter | 3/14/2019 |
| 15822 | PPD Richmond, VA Entry Level Scientist - Immunochemistry BS/BA in relevant field Exp: 0-2 years |
Responsibilities as a Entry Level Scientist include: Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/14/2019 |
| 15823 | PPD Middleton, WI Assistant Scientist- HPLC, GC BS/BA in relevant field Exp: 0-2 years |
Responsibilities as an Assistnat Scientist - HPLC include: Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. | 3/14/2019 |
| 15824 | PPD Middleton, WI Assstant Scientist BS/BA in relevant field Exp: 0-2 years |
Responsibilities as a assistant scientist include: Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/14/2019 |
| 15825 | PPD Austin, TX Med Tech I BS/BA in medical technology or NCA Exp: 0-2 years |
The Medical Technologist independently and without technical supervision performs low, moderate, and high complexity clinical laboratory testing as a generalist, with assignment in some or all of the following disciplines: urinalysis, coagulation, hematology, chemistry, special chemistry, and immunology. The Med Tech also troubleshoots laboratory equipment and methods and provides technical supervision of others as required. | 3/14/2019 |
| 15826 | PRA Health Sciences Chicago, IL Associate Regulatry Labeling Specialist BS/BA in science or health related field Exp: 0 years for associate level |
Responsibilities include: Provdies regulatory expertise/guidance for development and submission of US labeling components. Controls consistency of US labeling content through alignmnet with the core documents across product families and with all applicable best practicies. Must have a basic understanding of the drug development process and knowledge of the pertaining regulations | 3/14/2019 |
| 15827 | PRA Health Sciences Phoenix, AZ Application Developer - Health Data Services MS in computer sciences or related Exp: 1-2 years |
Candidate will be involved in developing and maintaining a portfolio of customer-facing solutions and applications. These projects will mainly include front end web and mobile developments, backend applications, and mobile content synchronization processes. Must have experience with ASP.Net, Python, Java and Javascript. | 3/14/2019 |
| 15828 | PRA Health Sciences Lenexa, KS Entry Level Clinical Trial Specialist BS/BA in science or health related field Exp: Entry Level |
As a clinical trials specialist, you are the primary point of contact/liaison for the sites. Sponsor internal stakeholders during study life cycle. Preform investigative site recruitment/feasibility, essential document collection and review, maintenance and close-out in-house site management activities in accordance with the Sponsor and/or PRA protocol. In addition, you will create and distribute meeting agendas and take meeting minutes during internal and sponsor calls, roll out training plans to team members and provide access to project systems. | 3/14/2019 |
| 15829 | PRA Health Sciences Los Angeles, CA Clinical Research Associate BS/BA in clinical, health or science related field Exp: 1+ years of clinical monitoring |
The Clinical Research Associate will monitor the progress of linical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and the reported in accordance with the protocol, SOPs, ICH-GCP, and other regulatory requirements. | 3/14/2019 |
| 15830 | PRA Health Sciences Salt Lake City, UT Lab Associate PRN BS/BA in medical, lab or life sciences Exp: 1-2 years in lab |
The Lab Associate is part of the operational team within the sample preparation alb. The Lab Associate ensure the appropriate collection, processing, storage and shipment of samples. Daily tasks may inolve maintenance of equipment, processing and shipment of samples. The Lab Associate is part of the study team that is responsible for the execution of the study. \ | 3/14/2019 |
| 15831 | PRA Health Sciences Lenexa, KS Medical Resaerch Associate/ Phlebotomist PT HS Diploma Exp: 1-2 years in medical or clinical field |
Duties include: Perform study specific clinical procedures, collect and record study data on CRF/SDs and interact with subjects during confinement and outpatient periods of clinical studies. Performs basic medical procedures according to protocol for specified study participants, include but not limited to informed consent, vital signs, Height/weight/BMI measurments, meals, water fast, phlebotomy, finger stick blood sugar, ECGS, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment, etc. | 3/14/2019 |
| 15832 | Precision BioSciences Durham, NC Research Associate, Bioanalytics MS in cell biology/immunology Exp: 1+ years in biopharma |
The Research Associate, Cell Therapy Bioanalytics works within the Cell Therapy Development Team and participates in providing bioanalytical support for Cell Therapy Process Development projects. The position will contribute to Bioanalytics development efforts for CART-cell projects by providing sample preparation and analysis in a timely manner. This position is lab-based and will share facilities and resources with the Cell Therapy teams. Daily responsibilities include: Execute bioanalytical methods for in-process sample analysis and cell product testing, Analyze generated data according to established SOPs and report results of analysis to Cell Therapy Team Leaders in a timely manner, Coordinate with Scientists, Research Assistants, and Research Associates to plan and carry out experiments for developing T Cell Therapies. | 3/14/2019 |
| 15833 | Precision Health Economics Los Angeles, CA Associate Research Scientist-Health Policy MS Exp: 1+ year conducting health economic research |
Collaborating across a broad portfolio of sophisticated health economic and health policy research projects. Performing a wide range of activities including: literature reviews; regression analysis; preparing content for reports and manuscripts, slide decks and meeting notes; quality assurance/review; and other activities. | 3/14/2019 |
| 15834 | Precision Health Economics New York, NY Associate Research Scientist - HEOR MS Exp: 1+ year conducting health economic research |
You will collaborate across a broad portfolio of sophisticated health economic and health policy research projects. You will perform a wide range of activities including: literature reviews; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. | 3/14/2019 |
| 15835 | Precision Health Economics Oakland, CA Associate Research Scientist-HEOR MS Exp: 1+ year conducting health economic research |
As an Associate Research Scientist/Research Scientist, you will responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. You will have a basic familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and will execute a wide range of activities including: project management; literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. | 3/14/2019 |
| 15836 | Precision Health Economics Boston, MA Associate Research Scientist-HEOR MS Exp: 1+ year conducting health economic research |
As an Associate Research Scientist/Research Scientist, you will responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. You will have a basic familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and will execute a wide range of activities including: project management; literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. | 3/14/2019 |
| 15837 | Pace Analytical Maplewood, MN Biochemist - Food Safety BS in biochemistry, microbio or related Exp: 1-3 years lab experience |
This candidate will perform testing as part of a product development team that deals with food safety. Responsibilities include: Perform allergen identification and measurement by ELISA and Lateral Flow Devices. Perform a wide range of general microbiology testing to include: particulate analysis, sterility testing, and microbial identification. Conduct analysis of products using traditional microbiological techniques such as serial dilution, pour plating, and filtration. Participate in general laboratory cleaning and maintenance. | 3/8/2019 |
| 15838 | Pace Analytical Lenexa, KS Laboratory Technician I - Entry Level HS Diploma Exp: 0 years |
Responsibilities of a lab technician include: Washing laboratory glassware. Responsible for keeping applicable workspaces clean and safe. Assisting other lab personnel with preparing samples, analysis, data checking and, and handling simple calculations. Disposing of samples and chemicals. Providing maintenance of stock reagents and lab supplies. Following company policies and Standard Operating Procedures (SOPs). | 3/8/2019 |
| 15839 | Pace Analytical Maplewood, MN Chemist - Entry-Level HPLC BS/BA in chemistry or related Exp: 0-2 years lab experience |
Candidate will perform analytical testing to support product development on inhalation devices. This is a high volume, fast-paced lab. Analytical lab experience is necessary, but fresh grads will be considered. Complete non-chromatographic tests such as: drug content, drug impurities, water content, dose content uniformity (DCU), through life testing, next generation impactor (NGI), particle size, spray pattern, microscopic appearance in support of stability, and other studies for development of an inhalation product | 3/8/2019 |
| 15840 | Pace Analytical Peachtree Corners, GA Laboratory Analyst I, Wet Chemistry BS/BA in scientific field Exp: 0-2 years |
Pace Analytical Services, LLC, a leading national analytical laboratory is seeking highly motivated candidates for a Laboratory Analyst I in the Wet Chemistry department at their laboratory in Atlanta, GA. Responsibilities include: Preparing and/or analyzing environmental samples based on published methods and Pace Standard Operating Procedures. Following quality control procedures as outlined in documented procedures. Preparing standards and reagents. Entering data into Pace Laboratory Information Management System (LIMS) as applicable. | 3/8/2019 |
| 15841 | Pace Analytical Peachtree Corners, GA Laboratory Technician HS Diploma Exp: <2 years |
Entry level position in laboratory services where work is closely supervised and done in accordance with well-defined standards and procedures of an uncomplicated nature. Responsibilities include: Analyzing or preparing samples in an efficient and organized manner, using approved Pace Analytical procedures. Preparing reagents and standards. Waste handling duties to include: labeling containers, understanding storage time limits, performing proper satellite accumulation, ensuring adequate space between waste containers, ensuring all waste containers are closed and incompatible materials are stored separately, understanding secondary containment, and documenting weekly inspections, if applicable. | 3/8/2019 |
| 15842 | Pace Analytical Ormond Beach, FL Laboratory Analyst - Semi-Volatiles BS/BA in sciences Exp: 0-2 years |
Tuesday - Saturday, 3 PM - 11:30 PM with possible overtime and weekend hours. Responsibilities as a lab analyst includes: Preparing and/or analyzing environmental samples based on published methods and Pace Standard Operating Procedures. Following quality control procedures as outlined in documented procedures. Preparing standards and reagents. Entering data into Pace Laboratory Information Management System (LIMS) as applicable. | 3/8/2019 |
| 15843 | Pacira Troy Hills, NJ QC Analyst I BS in chemistry Exp: 1+ years lab experience |
The purpose of this position is to carry out assigned laboratory duties which may include sampling, testing, and evaluating analytical data on samples such as raw materials, in-process and final products. Other responsibilities include: Maintain organized records of tests performed and results obtained. This may include maintaining a computer accessible database for the purpose of tracking and trending analytical data. Conduct laboratory tests in compliance with established internal Standard Test Methods, compendial methods and vendor partners supplied methods. Assist in the development and improvement of written procedures. | 3/8/2019 |
| 15844 | Pacira Troy Hills, NJ Research Associate II/Engineer I. BS in relevant field Exp: 1-4 years |
The purpose of this position is to assist in the scale up of manufacturing processes for new DepoFOAM formulations and the development of analytical methods to characterize materials for those efforts. Responsibilities include: Provide technical and analytical assistance to support new product development and process scale-up. Perform hands on work to set-up and execute experiments on bench-top, lab, and pilot scale manufacturing equipment. Support the technology-transfer of processes to the pilot and commercial scales to produce material for pre-clinical evaluation and clinical trials. Execute analytical methods for in-process and product material characterization, performing physical and chemical stability studies as needed. Maintain good working knowledge of the use, maintenance and repair of laboratory and manufacturing equipment. | 3/8/2019 |
| 15845 | Pandion Therapeutics Cambridge , MA Associate Scientist, Immunology Research BS or MS in relavent field Exp: 0-2 years |
Responsibilities include: Developand performin vitro/ex vivo human and murine primary cell-based assays. In vivo pharmacology including test article dosing, blood collection and tissue harvesting. mmune cell isolation from whole blood and tissues, flow cytometry, cell sorting,ELISA/MSD/HTRF. | 3/8/2019 |
| 15846 | Par Pharmaceuticals Rochester, MI Quality Associate II, Document Control AA/AS degree Exp: 1-2 years |
The Quality Associate II, Document Control follows the applicable Document Control SOPs and requirements in order to maintain a controlled environment within Document Control. This role, which is customer service oriented, works with various departments to either retrieve completed documents or generate new documents. Works in more complex areas of Document Control including APR documents, the Electronic Document Management System (EDMS), and management of documents during regulatory inspections. Provides guidance to the Document Control staff. Trains Quality Associate I, Document Control. Works with the team in maintaining a collaborative environment. | 3/8/2019 |
| 15847 | Par Pharmaceuticals Irvine, CA Quality Associate I - 2nd Shift HS Diploma Exp: 0-1 years |
The Quality Associate I, Operations is responsible for actively participating in “on the floor” Quality activities during product manufacturing and/or packaging. Quality activities include product sampling and inspection, area clearance to confirm process readiness, and non-conforming event support to resolve in-process issues. Communicates to multiple departments and supervision to provide timely process and issue updates. Identifies and escalates issues or problems to appropriate supervision. Participates as a team member on cross-functional teams. Participates in reviews and structured processes for continuous improvement. | 3/8/2019 |
| 15848 | Paragon Bioservices Harmans, MD Quality Control Analyst I-II - Environmental Monitoring AS/AA in life sciences Exp: 0-2 years GMP clean room experience |
This role is responsible for Environmental Monitoring sampling, analyzing, and aseptic monitoring and microbiological testing to support Phase I/II/III and Commercial GMP manufacturing. Key responsibilities include but are not limited to: Perform Environmental Monitoring of Grade B-D Cleanrooms, including sampling of viable surfaces, viable air and non-viable particulates in a Phase I/II/III/Commercial GMP Manufacturing facility. Conducts routine sampling and testing of Clean Utilities such as USP water (WFI) and clean steam. Conducts bioburden testing on prepared buffers/solutions, equipment cleaning samples, in-process and release drug product samples. Ability to isolate and sub-culture microorganisms for identification. | 3/8/2019 |
| 15849 | Paragon Bioservices Baltimore , MD Manufacturing Associate I - GMP Bioprocess AS/AA or BS/BA in scientific/engineering discipline Exp: 0-2 years |
The Manufacturing Associate performs and documents cGMP activities to support upstream or downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed. | 3/8/2019 |
| 15850 | Parexel Billerica, MD Drug Safety Associate Degree in Pharmacy, nursing or life sciences Exp: 0-2 years |
The Drug Safety Specialist will provide technical and process-related support to drug safety management (clinical trials) and medical monitoring activities, ensuring compliance with relevant regulations and Standard Operating Procedures (SOPs). Daily tasks include: Triage incoming reports for completeness, legibility and validity. Electronic documentation and quality control of drug safety information. Data entry of case reports into safety database / tracking system. | 3/8/2019 |
| 15851 | PBS Biotech Camarillo, CA Research Associate or Process Engineer, BioprocessR&D MS in life sciences or biotechnology Exp: 0-2 years |
This position is an invaluable opportunity to gain experience working withcutting edge technology and a variety of cell types that are significant to the rapidly emerging cell and gene therapy market. Responsibilities and tasks: Participate in research efforts for various cell culture processesbased on client needs. Prepare scientific data for external publications, abstracts, and presentations, including those atinternational conferences andtrade shows. Supportroot-cause analysis forunexpected results and provide new approachesor experimental strategiesfor problem solving | 3/8/2019 |
| 15852 | PCI Pharma Services Rockford, IL Validation Analyst 1 HS Diploma Exp: 1-3 years |
The Validation Analyst I is responsible for overall validation project ownership of limited risk project(s) under heavy supervision. Responsible for generation and execution of validation protocols, assistance in audits, and determination of validation needs. This job has no supervisory responsibilities. Primary duties include: Prepares validation protocols, validation statements, reports, summaries, and master validation plans for new customer / product / system project launch and maintains existing validated processes / programs at multiple sites as well as organizing and coordinating internal and customer approvals, as needed. Ensures validation documentation completion, accuracy, and closure, including organizing and coordinating multiple approvals as required. Investigates validation deviations, documenting in formal reports, and assuring resolution of corrective action to complete project. | 3/8/2019 |
| 15853 | PCI Pharma Services Philadelphia, PA Process Engineer BS in sciences or engineering Exp: 0-1 years |
The main functions of a Process Engineer are focused around two key activities of the production area: identifying and mitigating packaging issues for existing business through strong engineering and process improvement methods, and designing and supporting packaging processes for new business. Both activities are focused around technical and operational support to the production, maintenance, and support staffs in the areas of process improvement, equipment modification and optimization, safety and quality improvement, and increasing throughput. This is achieved through individual effort and facilitation of teams, tracking and analysis metrics, strong understanding and utilization of good engineering practices, project management, and the use of Lean Six Sigma techniques. | 3/8/2019 |
| 15854 | PCI Pharma Services Philadelphia, PA Packaging Designer BS in related field Exp: 1-5 years |
Reporting to Package Design Manager, successful Package and Graphic Designer would utilize technical design abilities and creative insights to help develop new innovative packaging. Utilizing design software, practical packaging knowledge, graphic design abilities and hands-on assembly skills, Designer would create and prepare design solutions for PCI clients to support sales efforts as well as provide clients recommendations for optimizing existing packaging. Designer may engage clients directly in support of package creation. In addition to primary role for package design/development, Designer would support Marketing design initiatives as required. Designer supports workflows and reliability of on-site prototyping laboratory, including supplies and maintenance | 3/8/2019 |
| 15855 | Penumbra Alameda, CA Quality Engineer BS/BA in engineering or scientific field Exp: 1-5 years in engineering |
As a Quality Engineer at Penumbra, you will participate in all aspects of product development, supplier development and manufacturing in order to ensure the highest level of quality in new and existing products, and their compliance to applicable regulations and standards. Responsibilities include: Represent Quality Engineering on New Product Development (NPD) cross-functional teams, interfacing among multiple departments and teams such as Manufacturing, QC, R&D, Regulatory Affairs, Operations/Planning, and Marketing. Troubleshoot, update, and improve difficult manufacturing processes for assigned product lines. | 3/8/2019 |
| 15856 | Penumbra Alameda, CA Regulatory Specialist BS in sciences or engineering Exp: 1+ years in regulatory affairs |
n this role, you will work with the team that ensures that Penumbra products are approved for use in countries around the world, thereby helping to bring our life-saving technologies to patients worldwide. Responsibilities include: Support the preparation of submissions to gain approvals for clinical research, export, and commercial distribution around the world. Support the creation, translation and review of labeling, Instructions for Use, and promotional materials. Develop a working understanding of the Quality System, biocompatibility requirements, Design Control, Medical Device Directive, Essential Requirements, ISO 13485, labeling requirements, Quality System Regulation, Canadian regulations, export requirements, and regulatory requirements of pertinent regions. | 3/8/2019 |
| 15857 | Performance Validation Indianapolis, IN evel 1 Staff Validation Engineer / Specialist BS in life sciences or technical field Exp: Entry Level |
The Level 1 Validation Engineer/Specialist works within a small team environment to provide technical services to pharmaceutical or medical device manufacturers. Technical services may include interpreting drawings, manuals, or other technical information to develop requirement documents, developing testing documents that verify installation, and/or operation of the equipment, and execution /documentation of these testing documents. These documents are used by our life science customers to demonstrate compliance with USFDA regulations (or other regulatory bodies) for current Good Manufacturing Practices. | 3/8/2019 |
| 15858 | PerkinElmer Thousand Oaks, CA Associate Lab Ambassador-Thousand Oaks, CA BS/BA Exp: 1+ years in customer service |
Provide high touch support for the scientist community of designated functional group(s) at designated account and general support for the on-site service engineers and technicians. Coordinate and communicate with end users regarding all aspects of OneSource Asset Management program, including service call initiation, scheduling, maintenance, inventory data integrity, escorting of vendors for “managed” activities, safety and day-today lab operations. | 3/8/2019 |
| 15859 | Perrigo Covington, OH Microbiologist - 1st Shift/Rotating 2/2/3 Schedule BS in biological, or food sciences Exp: 1+ years in GMP environment |
Responsibilities include: microbiology (aerobic plate counts, probable number analysis, isolating/identifying bacterial cultures, ELISA, PCR, etc.) and routine lab functions (data entry, maintaining bacterial control cultures, instrument maintenance, etc.) | 3/8/2019 |
| 15860 | Perrigo Allegan, MI Associate Packaging Engineer BS/BA in packaging engineering or other engineering Exp: 0-6 years |
Provides comprehensive package engineering support and packaging component expertise to the company through the design, development, and maintenance of packaging standards for various company and outside sub-contracting product packaging sites. Responsibilities include: Troubleshoots and resolves packaging issues associated with packaging component quality, packaging equipment, and packaging line efficiency, participates in packaging component deviation resolutions, and coordinates, conducts, and documents packaging line trials for new or improved packaging components. Works closely with other functional areas and multi-functional teams such as Operations, Sales, Marketing, Procurement, Contract Customers, Contract Packagers, Master Data, Art and Quality to launch new products/packages, develops promotions and displays, develops cost savings initiative, and troubleshoots packaging problems. | 3/8/2019 |
| 15861 | Personalis Menlo Park, CA Laboratory Assistant BS in life sciences or related Exp: 0-2 years |
We are looking for a team-oriented Laboratory Assistant to join our operations team. The ideal individual must have the ability to think on their feet and troubleshoot issues. Responsibilities include: Adhere to the laboratory's quality control policies. Participate in laboratory support work as required by the team needs and at the direction of laboratory management. Following the laboratory’s procedures for specimen handling, receipt and data entry into the lab information management system (LIMS). Maintain lab equipment. Etc. | 3/8/2019 |
| 15862 | Pfenex San Diego, CA Associate Scientist I MS in biology, chemistry, or related Exp: 1+ years lab experience |
Pfenex is looking to bring on a contract Associate Scientist 1 , to join the Analytical Sciences team. As a key member of the Analytical Biochemistry Group, the Associate Scientist I ,is responsible for executing analytical and biochemical characterization activities for biotherapeutic protein product development, including assay development, assay qualification, and product characterization. This position must effectively communicate timelines and issues to ensure successful manufacturing, product testing/release and data package for regulatory filings. Individual technical issue management and cross functional communication are key position attributes. The candidate will work in a team environment, collaborating with various departments to ensure that manufacturing processes are properly characterized to support process transfer, achieve project goals, and timelines. | 3/8/2019 |
| 15863 | Nurx Syracuse, NY Pharmacy Technician HS Diploma or BS Exp: 1+ years as pharmacy technician |
Weekend and On-Call Position. Responsibilities and duties include: Process and key-in prescriptions with accuracy, attention to detail, and efficiency. Correctly input sensitive prescription information into computer system, dispense correct medication, and verify information before releasing prescriptions. Demonstrate knowledge of Third Party insurances and billing procedures. Proactively partner with the Pharmacy, Operations and Engineering teams to address issues and achieve high quality and throughput in fast-growing, technology-empowered pharmacy. | 3/7/2019 |
| 15864 | NuVasive San Diego, CA Assoc Test Engineer, Validation MS in computer science, engineering or related Exp: 1+ years |
As the Validation Engineer, you will ensure the quality of the medical device software and hardware meets the design requirements and that they are testable. You will also develop, implement and maintain test plans, protocols, test scripts and traceability matrix for design verification & validation. Essential responsibilities include: Execute protocols/test scripts and document results. Generate and/or update summary reports. Ensure compliance with FDA device regulatory requirements, including DHF and 510(k). Communicate with Hardware and Software Development, Marketing, Technical Services, and other project team members to ensure schedules and requirements are consistent with project expectations. etc. | 3/7/2019 |
| 15865 | NuVasive Richmond, VA Associate Neurophysiologist BS or CNIM Elgible Exp: 0-1 years |
Health care professional responsible for real time data collection and monitoring of a patient’s nervous system throughout surgery. In addition, he/she must establish and maintain open cooperation and communication with the surgical team, which includes interaction with the surgeon. Additional responsibilities include pre-operative patient assessments and post-operative billing uploads. Responsibilities: Consult with surgeon regarding structures at risk and modalities to be monitored. Interact with patient, when applicable, to obtain a detailed history and clearly explain the neurophysiological tests to be performed. Display and label waveforms for marking, measuring and calculating information such as latencies, amplitudes and conduction times following established guidelines and protocols. Communicate with the surgeon and surgical team throughout the case to relay monitoring information. | 3/7/2019 |
| 15866 | NuVasive West Carrolton, OH Manufacturing Engineer BS in technial engineering discipline Exp: 1+ years |
As the manufacturing engineer, candidate will be responsible for: Coordinate cross-functional teams to execute and document the manufacturing launch of new/legacy products. Determine manufacturing processes required to accurately and efficiently make spinal implants, from raw material to final cleaning and shipment. Develop and complete manufacturing documentation (pFMEA, control plan, process flow, work instructions, and inspection plans). Perform research, design, and development of manufacturing processes including production flow, assembly methods, and production equipment. Perform product/process analysis and troubleshooting for cost reduction, quality improvement, and improved efficiency. Design, develop, test, source, and cost-justify various tools, machinery, and equipment for recommended manufacturing methods. | 3/7/2019 |
| 15867 | NuVasive Memphis, TN Associate Sterile Processing Tech HS Diploma Exp: 1+ years |
Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties. Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. etc. | 3/7/2019 |
| 15868 | NxStage Lawrence, MA Test Engineer I BS in engineering Exp: 1-3 years |
The individual in this position will support product development and lead test-related activities related to the development of NxStage Medical’s equipment and disposable products. Responsibilities include: Work closely with all engineering disciplines, including Systems, Electrical, Mechanical, Disposables, and Software Engineering, as well as Project Management and Quality personnel, to verify and validate product designs. Participate in the planning and lead the execution of Validation & Verification (V&V) testing activities in support of regulatory filings for Class II medical devices. Specify, design, and develop test systems (hardware & software); ensure that all test systems and equipment are appropriately validated and controlled. Manage V&V documentation, including derivation of Test Procedures from System and Sub-System Specifications, validation of Test Procedures and Test Fixtures, and generation of test reports. | 3/7/2019 |
| 15869 | Ology Bioservices Alachua, FL Downstream BioManufacturing Process Associate BS/BA in science or engineering Exp: 0-2 years in biologic based GMP |
This position will assist production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). Responsibilities include: Perform and/or assist with downstream related activities including Chromatography purification, Centrifugation and Ultracentrifugation, Ultrafiltration/Diafiltration, Viral Clearance. Draft Standard Operation Procedures, Change Control, Deviations. Properly disinfect and stage materials into production rooms before the production campaigns. Assist with equipment ordering, installation, qualification and routine maintenance. Perform activities to support production campaign such as preparation of tubing assemblies, autoclave, material request and transfer into production room. | 3/7/2019 |
| 15870 | Ology Bioservices Alachua, FL Upstream Biomanufacturing Process Associate I BS in biology, chemistry ore equivalent Exp: 0-2 years |
This position will assist production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). Responsibilities include: Perform and/or assist with upstream related activities including Cell culture at small and large scale, Cell transfection, Media and buffer preparation, Bioreactor and Fermentor based production. Draft Standard Operation Procedures, Change Control, Deviations. Write raw material specifications, research, source and order material and lab wares. Perform activities to support production campaign such as preparation of tubing assemblies, autoclave, material request and transfer into production room. | 3/7/2019 |
| 15871 | Olympus Richmond, WA Research Scientist I BS in biomedical engineering or related Exp: 0-1 years |
The Research Scientist I assists and participates in biomedical, pre-clinical and clinical research and development projects, experiments, and investigations relevant to the Company’s product strategy or services, disseminating findings through internal reports. This is an entry level research position. Job duties include: Support the design and implementation of research and/or engineering development projects. This may include but is not limited to, support of in-vivo (animal) and ex-vivo testing. Collaborate with other functional groups including product development, clinical and regulatory to fulfill project deliverables. Assist with the execution of clinical research investigations and product evaluations. Create and maintain files related to the pre-clinical and clinical activities. | 3/7/2019 |
| 15872 | Olympus Waltham, MA Mechanical Engineer II (Document Control) BS in engineering or equivalent experience Exp: 1+ years with design drafting in manufacturing |
As a Mechanical Engineer II on the Engineering Services team, you will be empowered and inspired to do your best work. You will contribute to our mission by helping to support new product introduction and improve existing and new XRF and XRD products that help make the world a safer place. In your role, you will help to improve efficiencies on the production floor by working with Production Engineering in the design and documentation of production fixtures and tooling. In a typical day, you will: Design production fixtures and tooling. Translate concepts to final designs and documentation complete with Bills of Material. Resolve product/process problems, support development of new products/processes, initiate technical investigations, and prepare design specifications, analyses, and make recommendations for presentation and approval. | 3/7/2019 |
| 15873 | Olympus Richmond Hill, Ca Endoscope Technician I - Recovery HS Diploma Exp: 1+ years in technical repairs |
The Endoscope Technician must understand and accept the responsibility to ensure the safety of all Olympus products that are repaired by strictly following established processes and procedures. Under the direction of the Manager, the incumbent shall evaluate, troubleshoot, disassemble, assemble, repair and inspect Endoscopes, Electronics, or Microscopy products to meet company product standards and ensure full and proper functioning of the repaired product. Level I Technician: Assignments are semi-routine difficulty level. Requires daily supervision, detailed instruction on new assignments. | 3/7/2019 |
| 15874 | Olympus Waltham, MA Production Test Technician II HS Diploma Exp: 1+ years in technical repairs |
The Production Test Technician II will perform the set-up, calibration, testing and troubleshooting of circuits, components, instruments and mechanical assemblies. Follow methods and procedures from drawings, diagrams and test plans. May complete rework on assemblies and / or systems as a result of testing. Job duties include: Adhere to policy and procedures to maintain a safe and clean work environment. Apply acquired job skills, company policies and procedures to complete assigned tasks and adherence to production plan schedules while producing high quality products to standards. Advise management of adverse manufacturing and/or equipment conditions and issues that are affecting production and /or safety. | 3/7/2019 |
| 15875 | Olympus Multiple Locations, na Field Service Engineer I AS or BS/BA in electrical, biomedical, or computer sciences Exp: 1+ years of servicing/reparing electronics |
As a Field Service Engineer I working on the Field Service team, you will be empowered and inspired to do your best work. You will contribute to our mission by providing our customers with the best support and repair solutions, assisting our field sales teams with installations and maintenance of equipment and contributing to the growth of the division. Duties will incude: Performing new equipment installations, upgrades, post installation testing, troubleshooting and all other aspects of technical support for all endoscope, mechanical, electronic, video, computer, LAN and network products. Troubleshooting, diagnosing, and repairing the entire line of medical electronic, video, computer and network products on customer premises, at Olympus repair facilities, and when necessary via telephone. Escalating support issues when customer satisfaction is jeopardized and report all product non-conformance and safety concerns. | 3/7/2019 |
| 15876 | Oncotherapy Solutions LLC Seattle, WA Research Associate I MS in biological sciences Exp: 1+ years |
Oncotherapy Solutions LLC is seeking a highly motivated and creative research associate to characterize and test drug conjugates in-vitro as well as analyze tissue and blood samples from outsourced in-vivo studies. Responsibilities include: Perform solubility and in-vitro stability assays as well as formulation of drug conjugates. Conduct viability and apoptosis in-vitro assays using cancer cell lines, normal cells and immortalized non-tumorigenic cell lines. Extract and purify nucleic acids and proteins from cells, tumor and normal tissues as well as perform RT-PCR, PAGE, western blotting and ELIZA. | 3/7/2019 |
| 15877 | Thermo Fisher Scientific Saint Louis , MO Scientist I, Analytical and Formulation Sciences BS in biology, chemistry ore equivalent Exp: 0-2 years |
Perform various chromatography assays including reverse phase, size exclusion, affinity and ion exchange chromatography. Participate in analytical studies to support method and formulation development, structural characterization, comparability, forced degradation, and other development activities of biopharmaceuticals at all stages of clinical development. Conducts routine tasks and sample analyses to support process development. Executes, records, and evaluates experimental data appropriately, including the writing and revising of process development reports and technology transfer protocols as needed. | 3/7/2019 |
| 15878 | Thermo Fisher Scientific Cincinnati, OH Research & Development/Manufacturing Scientist I BS/BA in science or engineering Exp: 0-2 years in metrology support |
Provides Metrology support in a laboratory environment by following standard practices. Performs laboratory instrument calibrations, qualifications, preventative maintenance, and repairs as assigned. Makes detailed observations and reviews, documents, and communicates test results. Essential functions include: Executes test methods for instrumentation including, but not limited to; LC, GC, dissolution, spectroscopy, pH meters, thermometers, and balances. Recognizes and reports out-of-specification or unexpected results and non-routine instrument mechanical performance problems. Supports routine instrument preventative maintenance and troubleshoots unplanned mechanical repairs. | 3/7/2019 |
| 15879 | Thermo Fisher Scientific Cincinnati, OH Research & Development/Manufacturing Scientist I BS/BA in science or engineering Exp: 0-2 years in metrology support |
Provides Metrology support in a laboratory environment by following standard practices. Performs laboratory instrument calibrations, qualifications, preventative maintenance, and repairs as assigned. Makes detailed observations and reviews, documents, and communicates test results. Essential functions include: Executes test methods for instrumentation including, but not limited to; LC, GC, dissolution, spectroscopy, pH meters, thermometers, and balances. Recognizes and reports out-of-specification or unexpected results and non-routine instrument mechanical performance problems. Supports routine instrument preventative maintenance and troubleshoots unplanned mechanical repairs. | 3/7/2019 |
| 15880 | Thermo Fisher Scientific Greenville, NC Formulation Technician HS Diploma Exp: 1+ years in manufacturing/productions |
Sets-up, operates, and maintains the classified environments and manufacturing equipment for pharmaceutical products. Requires proficiency in; cleaning and sterilizing equipment, gowning and aseptic techniques, preparing equipment and components for operations, operating and troubleshooting mechanical equipment, following approved procedures and proper documentation. | 3/7/2019 |
| 15881 | OPKO Diagnostics Woburn, MA Research Associate, Conjugation Chemistry BS in chemistry/biochemistry Exp: 1-2 years |
OPKO Diagnostics is seeking a highly motivated Research Associate with a Bachelor's degree in Chemistry or Biochemistry and/or prior hands-on experience in bioconjugation and purification to join our research group in Woburn, Massachusetts. As a member of the R&D group, you will be working closely with in-house expert in conjugation chemistry and contribute to the development of innovative diagnostics tests on the Claros Analyzer platform. Responsibilities include: Plan, perform and document protein modification and bioconjugation experiments. Prepare, purify (e.g. HPLC, continuous gel electrophoresis) and analyze (Native and SDS PAGE) protein and antibody conjugates. Conduct experiments to improve efficiency and scalability of conjugates to support routine manufacturing. | 3/7/2019 |
| 15882 | OPKO Diagnostics Woburn, MA Research Associate BS or MS in biology, chemistry or related Exp: 1+ years lab experience |
We are looking for a Research Associate with interest and experience in commercial product development for IVD immunoassays. The candidate will contribute to assay development activities on OPKO’s proprietary microfluidic cassette/platform. Responsibilities include: Design, plan, perform, and document product development activities, including immunoreagent development, immunoassay optimization, and analytical/clinical studies. Troubleshoot experiments, consult literature and actively propose/pursue solutions. Assist in the design and development of assays on the Claros platform, contribute to regulatory activities with development reports, and participate in verification / validation activities. | 3/7/2019 |
| 15883 | Oranogenesis La Jolla, CA Manufacturing Associate I - DG Growth Biotech Program certification Exp: 0-1 years |
Manufacturing Technician I is responsible for completing and assisting with daily tasks associated with cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Additionally, the Technician I will be responsible for following SOPs, performing daily tasks in a clean room/cGMP environment per the current QSRs. The Manufacturing Technician I may also be responsible for the troubleshooting of manufacturing challenges. Follows established company rules, regulations and safety precautions, and maintains quality standards. | 3/7/2019 |
| 15884 | Oranogenesis La Jolla, CA Lab Associate I/II BS/BA in life sciences Exp: 0-2 years lab experience |
The candidate will be involved in a variety of activities including but not limited to: working on biomaterial and cell based studies; general lab support and maintenance; materials testing; running established assays. The individual will participate in the execution of experiments in a team environment or independently post adequate training, and will support the data analysis and reporting of results as needed. | 3/7/2019 |
| 15885 | Origene Rockville, MD Research Associate - Immunology BS in biology, chemistry or life sciences Exp: 1-2 years lab experience |
Responsibilities include: Involves multiple de novo R/D projects for antibodyand assay products development.Performsvalidation tests on variant sera or antibody samples. Participates other duties such as antibody production, purification and conjugation. Records experiment procedure and results in notebooks and computer accurately. etc | 3/7/2019 |
| 15886 | Orthofix Lewisville, KY Design Assurance Engineer BS in mechanical engineering or related Exp: 0-2 years |
This position is responsible for providing Design Assurance support to product development activities within Orthofix supporting all new product development and selected sustaining or specials projects in Orthofix. The position will report to the Quality Director. The position must also ensure compliance with applicable product standards, governing laws and regulations, and company quality system requirements. Responsibilities include: Root cause analysis, problem solving, continuous improvement and related corrective and preventive action as they relate to complaints, non-conforming material, post-market surveillance (PMS), and other quality data, Quality Planning, Input and approval for design verification and validation testing of new designs and design changes to ensure product design quality and integrity. | 3/7/2019 |
| 15887 | Orthofix Lewisville, KY Development Engineer BS in mechanical or biomedical engineer Exp: 0-2 years |
Entry level engineering position responsible for supporting projects lead by more senior engineers. Responsibilities include: developing CAD models/drawings, authoring test protocols and reports, performs product testing, etc. | 3/7/2019 |
| 15888 | Osiris Columbia, MD Equipment Specialist AS/AA in biomedical technology Exp: 0-2 years |
Equipment Specialist will perform a variety of functions associated with the selection, acquisition, implementation, and qualification (FAT, IQ, OQ, and PQ) of all equipment and systems related to the laboratories, logistics, and manufacturing departments. The Equipment Specialist will assure that all equipment and systems operate in a safe and sound manner through proper calibration, maintenance, and repairs while developing and providing proper functionality training to others. Under the supervision of management, will have the oversight of contractors performing maintenance and/or service activities on equipment and systems. Will confer with management to identify equipment and systems with areas of concern and prioritize projects based on need. | 3/7/2019 |
| 15889 | Osiris Columbia, MD Biotechnology, Document Control Specialist AS or BS/BA in sciences Exp: 1+ years in regulated environment |
The primary purpose of this position is to issue batch production records and product labels to manufacturing in a timely manner to meet the production schedule. Principle responsibilities include: Assignment of product lot numbers and issuance and inspection of batch records associated with each manufacturing process. Generation and inspection of complex product labelling for all products in current production, including the ability to identify minute defects on printed labels. Coordinating printing schedule based on production plan to ensure manufacturing operations are not halted through lack of batch records or product labels. Maintaining controlled area inventory, packing and verifying quality records to be sent to off-site storage. | 3/7/2019 |
| 15890 | Osmotica Pharmaceuticals Marietta, GA Analytical Chemist I BS in chemistry, biochemistry or related Exp: 0-5 years |
The Analytical Chemist is responsible for testing of raw materials, in-process materials, and finished products to support release and stability programs. Perform laboratory tests such as sample extractions, set up and execution of chromatographic methods (HPLC and GC), and dissolution testing. Develops and executes UV, IR and PSD measurements and wet techniques as applied in the Pharmaceutical Analysis/Testing of products and excipients. Executes components of method validation and method transfer projects. | 3/7/2019 |
| 15891 | AMRI Rensselaer, NY Research Scientist I BS or MS in chemistry or related Exp: 0-5 years in medicinal chemistry |
The Research Scientist I/II is an integral part of the AMRI team, contributing to our success by the synthesis, purification and identification of intermediates and target compounds. Responsibilities include: Synthesize compounds efficiently using literature or in-house notebook procedures. Purify synthesized chemicals to an appropriate degree. The scientist will be able to use the full range of chromatographic, crystallization, and distillation techniques. Analyze and identify compounds using a good range of modern separation and spectroscopic techniques. This will include interpretation of TLC, HPLC, polarimetry, IR, and NMR spectra of moderate complexity. | 3/7/2019 |
| 15892 | AMRI Lebanon, NJ Quality Assurance Associate BS/BA in chemistry or related Exp: 0-2 years |
The Package Testing Technician is an integral part of the AMRI team, contributing to our success by performing data review, auditing laboratories, investigation/corrective action follow-up, and reviewing written procedures. Responsibilities include: Independently perform duties, both routine and non-routine, completed in a reliable and accurate manner. Endure the integrity of the final report of analysis being in compliance with all regulatory and company standards. Primary QA reviewer of all analytical data generated in the laboratory and performs weekly review of all logbooks, temperature tracking documents and any other related logs maintained in the laboratory. | 3/7/2019 |
| 15893 | AMRI Alburquerque, NM Chemist I BS/BA in chemistry or related Exp: 0-2 years |
The Chemist I is responsible for support of the manufacturing department and external customers. The routine functions of the laboratory are testing of raw materials, in-process, end product, and stability samples. The Chemist I will also performs particulate testing and tests plant water for production. The chemistry department is responsible for the successful transfer of new customer products and method testing. Perform routine laboratory testing tasks using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, Total Organic Carbon analyzer. Have the potential and willingness to train on new techniques | 3/7/2019 |
| 15894 | AMRI West Lafayette, IN Research Scientist I BS/BA in chemistry or related Exp: 0-1 years |
The Research Scientist I is an integral part of the AMRI team, contributing to our success by performing laboratory experiments and instrumental testing in the Analytical Development group. Responsibilities include: Conduct laboratory experiments as part of development and validation of solid-state chemistry analytical methods to support drug development processes, including but not limited to preparation of solid-state mixtures and studies of solid-state attributes of materials. Perform routine instrumental testing according to study design and under the guidance of the project leader. | 3/7/2019 |
| 15895 | AMRI Alburquerque, NM Microbiologist I BS in life sciences Exp: 0-2 years lab experience |
Prepare, collect, and test plant purified water, manufacturing raw materials, product in-process, and finished product, and perform environmental monitoring. With limited supervision, learn and perform critical laboratory techniques and complete original work. Author problem reports and participate in investigations. This description is inclusive of EM and testing duties: actual percentages of time spent on each duty may vary based on business needs. | 3/7/2019 |
| 15896 | AMRI Burlington, MA Microbiologist BS in life sciences Exp: 1 year in GMP/GLP environment |
The Quality Control Microbiologist performs quality activities in support of product production and releases. The QC Microbiologist performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. Some responsibilities include: Perform microbiological testing (endotoxin, sterility and bioburden) for raw materials, in-process materials, intermediates and final product. Perform environmental monitoring of the clean rooms (under ISO and EU specifications). Read, trend and report environmental, personnel, in-process, raw material, finish product and water bioburden testing results. | 3/7/2019 |
| 15897 | Novartis Lake Forest, CA Mechanical Engineer BS/BA Exp: 0-4 years |
In this role, the incumbent conducts process research, process development and process upscaling for new medical device products. She/He also investigates and evaluates existing technology and designs new methodology, materials, machines and/or processes as needed for medical device development. Responsible for leading, participating in or supporting the product development activities such as prototyping/testing, pilot builds, verification & validation testing, risk assessment and production tooling validation. Generates detailed fabrication drawings, appropriate product requirements and technical file documents and leads design reviews. Responsible for the design and development of mechanical components, systems, and products using PTC Creo | 3/2/2019 |
| 15898 | Novavax Rockville, MD Bioprocess Associate I BS/BA Exp: 1-2 years in lab or cGMP |
We are seeking a highly detail-oriented and organized individual to support Process Development with the manufacture of buffers and media. Additionally, this individual would be responsible for managing the PD inventory program. Main function will be to perform the day to day activities in the Solutions Preparation Area: preparation of buffers, preparation of cell culture media/feeds, calibration of pH and conductivity meters/probes, transport of glassware, scheduling equipment maintenance, etc., to support all of process development. | 3/2/2019 |
| 15899 | Novavax Gaithersburg, MD Lab Support I Degree in scientific discipline Exp: 0-2 years in cGMP lab |
Individual is responsible for ordering lab supplies by inventorying stock; placing orders; verifying receipt, restocking lab and discarding expired reagents. Individual will track critical reagent supplies and notify affected personnel when supplies are low. Individual will maintain laboratory equipment by following standard operating procedures; maintain equipment related supplies, record and maintain equipment temperature logs. Individual will be responsible for performing daily/weekly and monthly equipment (Biosafety cabinets, incubators, water baths, plate washers, refrigerators, freezers etc) cleaning as per laboratory schedule. | 3/2/2019 |
| 15900 | Novodiax Hayward, CA Innovation Scientist BS degree in biology or related Exp: 0-2 years lab experience |
Candidate will be responsible for development and optimization of tissue-based assays. Individuals will have a background in biology or a related discipline and laboratory experience in human and animal tissue preparation, histological staining, and immunohistochemistry (IHC). Individuals must be self-motivated and detail-oriented, exhibit excellent organizational and communication skills, as well as demonstrate the ability to work under defined timeframe, thrive with a high degree of independence and be a team-player. | 3/2/2019 |
| 15901 | Novozymes Houston, TX Lab Technician HS Dipolma Exp: 1+ years |
The Lab Technician will inoculate spores from a stock culture onto petri plate medium for growth and manually harvest spores after growth into sterile carrier. This position will also maintain accurate records of inoculation and harvest plates. We are looking for someone who can follow directions carefully and accurately, proven initiative, communication skills and ability to gain respect and cooperation of others throughout the organization. | 3/2/2019 |
| 15902 | Novum Fargo, ND Entry Level Technicians HS Dipoma Exp: 0-1 years |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 3/2/2019 |
| 15903 | Novum Las Vegas, NV Research Technician Hs Dipolma Exp: 3+ months |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 3/2/2019 |
| 15904 | Novum Pittsburgh, PA Data Coordinator BS/BA Exp: 0-2 years |
The Data Coordinator will be responsible for assisting in the design, implementation and delivery of high quality clinical data within project timelines. Will execute data queries; perform medical coding, data reconciliation for study databases, and tracks data clarifications. Assists in the design of study start up documents i.e. Data Management Plan, eCRF, spec design, and edit check specs | 3/2/2019 |
| 15905 | Natera San Carlos, CA Clinical Laboratory Associate I (Temporary) BS/BA in biological sciences Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate I (Temporary) to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. Primary responsibilities include: Assists in testing of patient samples according to standard operating procedure in an efficient manner with little to no errors, Responsible for maintaining updated understanding and knowledge of methods performed in the lab, Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire. | 2/28/2019 |
| 15906 | Natera San Carlos, CA Clinical Data Operator 1 HS Dipolma Exp: 0-1 years |
Clinical Data Entry Operator 1 accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. Primary responsibilities include: Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning, Accession samples with high accuracy and efficiency, Protect patient health information (PHI) at all times to ensure compliance with HIPAA and privacy policies. | 2/28/2019 |
| 15907 | Natus Medical Chicgo, IL Engineer, Product Implementation BS/BA Exp: 0-2 years |
Natus is seeking a Product Implementation Engineer for our Midwest region. This position is responsible for working with customers on Neuro product line site-specific server planning for SQL, Citrix, and HL7; server implementations, and post-installation support. The qualified individual will provide input to product development teams on such products and train technical support as required to support such products and may be called on to visit customer sites for the installation, in-service, and repair of the company's supplied equipment. | 2/28/2019 |
| 15908 | Navitor Pharmaceuticals Cambridge, MA Research Associate BS/BA or MS in biology or related Exp: BS: 1-2 years, MS: 0-2 years |
We are seeking highly motivated, energetic and committed individuals to join our interdisciplinary team and actively contribute to advancing our drug discovery programs from discovery to proof-of-concept. You will build your experience in early discovery projects using cell-based and biochemical/biophysical approaches to support small-molecule discovery activities and advance our cutting-edge programs that target the mTORC1 pathway | 2/28/2019 |
| 15909 | Nektar Biologics Huntsville, AL Process Technician II BS in chemistry, biochemistry, chemical engineering or related Exp: 0-2 years |
Operates production equipment. Weighs, measures and checks raw materials to ensure batches manufactured contain proper ingredients and quantities. May help in validating processes and equipment that are directly related to filtration, cleaning and sterilization. Maintains records and clean room environment to comply with regulatory requirements, good manufacturing practices and standard operating procedures. Works on projects that are moderately complex in nature. Exercises judgment in resolving problems and making some routine recommendations. Provide Lab Support for manufacturing suites. Learn how to run equipment, read and understand SOPs. Support processing by adhering to SOPs. Follow HazMat procedures, for movement of Raw Material used in chemical processes. Support investigations Review SOPs. Troubleshoot and offer ideas on improvements. Interact with other departments to share information. Performs other duties as assigned. |
2/28/2019 |
| 15910 | Nelson Laboratories Salt Lake City, UT Lab Analyst - Sun - Thurs, 9am-5:30pm BS/BA in relevant sciences Exp: 0-2 years |
he Laboratory Analyst conducts testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. | 2/28/2019 |
| 15911 | NemaMetrix Eugene , OR Laboratory Technician I, Biology BS in biology or related Exp: 1 year |
This is a collaborative, team‐based role with the responsibility to perform Molecular Biology and C. elegans screening tasks for R&D discovery and development projects. Responsibilities include: Perform molecular biology assays including PCR, qPCR, and gel electrophoresis. C. elegans culture and maintenance. Working knowledge of basic laboratory equipment and protocols, including solution preparation and dilution series.This is a collaborative, team‐based role with the responsibility to perform Molecular Biology and C. elegans screening tasks for R&D discovery and development projects. Responsibilities include: Perform molecular biology assays including PCR, qPCR, and gel electrophoresis. C. elegans culture and maintenance. Working knowledge of basic laboratory equipment and protocols, including solution preparation and dilution series. | 2/28/2019 |
| 15912 | Neogen Lansing, MI QC Technician I AS/AA in sciences Exp: 1+ years |
The QC technician I position requires the candidate to perform routine biological and chemical assays daily. Other responsibilities include assisting supervisors with improving procedures, participating in troubleshooting and meeting goals and objectives. The ideal candidate would have laboratory experience at a college or industrial setting. | 2/28/2019 |
| 15913 | Neogen Lexington, KY Diagnostic Production Technician I HS Dipolma Exp: 0-2 years |
The Diagnostic Production Department for Neogen Corporation is seeking candidates for a technician position responsible for manufacturing, packaging, and assembly of diagnostic test kit components. The ideal candidate will be reliable, possess attention to detail, and able to work in a fast-paced environment. Responsibilities include: Sets up, adjusts, and operates laboratory equipment and instruments including, but not limited to: balances, microplate dispensing equipment, reagent dispensing equipment, bottle cap tightener, and labeling equipment. Cleans and maintains work areas and equipment used in daily manufacturing duties. Produces and packages plates approved by QC Department. | 2/28/2019 |
| 15914 | Neogen Lansing, MI Production Chemist BS/BA in biology, science, or food sciences Exp: 1-3 years |
Formulate batch reagents needed to meet production schedule using standardized manufacturing documents. Assist in establishing protocol for manufacturing new products. Essential Duties and Responsibilities include the following. Other duties may be assigned. Formulate chemical reagents from stock with direction from the appropriate Standard Manufacturing Procedure (SMP) or Standard Operating Procedure (SOP). Conduct chemical (immunological) reactions for development of reagents with direction from the appropriate Standard Manufacturing Procedure (SMP) or Standard Operating Procedure (SOP). Assist in process transfer from R&D to Manufacturing Department with direction from the appropriate Standard Manufacturing Procedure (SMP) or Standard Operating Procedure (SOP). | 2/28/2019 |
| 15915 | Neogen Lansing, MI Lateral Flow Chemist BS/BA in chemistry, biochemistry, or related Exp: 1+ years |
The Food Safety Division is currently seeking a candidate for a Lateral Flow Chemist position. The selected candidate would be responsible for formulating reagents and preparation of some components used in the assembly of Diagnostics and Dairy Antibiotics Lateral Flow products. Other duties would include testing and documenting results following ISO and GMP procedures. The ideal candidate should have the ability to perform basic mathematical operations, follow and document all manufacturing procedures, be capable of identifying and resolving problems in a timely manner and be able to work both independently, as well in a group setting. The selected candidate will be responsible for preparing buffers, solutions, and reagents according to Standard Manufacturing Procedures (SMP’s) and Work Orders, while maintaining an accurate inventory of chemicals and supplies. | 2/28/2019 |
| 15916 | Neogen Lincoln , NE Lab Technician - Processing BS/BA in scientific discipline Exp: 0-2 years |
Performs laboratory tests and services to support customer data generation within the platform specific processing lab, through a variety of scientific techniques, instrumentation, and disciplines by performing the following duties: Gain and maintain the ability to operate all electronic and robotic equipment essential to primary platform processing. This includes all hand held electronic repeaters, multichannel pipettes along with liquid handling robots. Maintain consistency and quality in lab techniques and procedures within an ever changing and fluid work environment. Accurate record keeping which includes but is not limited to laboratory notebooks, lot record tracking, sample archives, LIMS and/or repository as necessary. | 2/28/2019 |
| 15917 | Nephron Pharmaceuticals West Columbia, SC Quality Assurance OnlineEvening 12 hour Shift ONLY HS Dipolma Exp: 1+ years |
Performs Weight Check and Quality Attributes Inspection of the product through the filling and packaging process in compliance with company policies / procedures, FDA and cGMP regulations. Ensures the accuracy and completeness of batch records. Monitors and perform start up, in-process and finished product inspections including weighing. Monitor all production areas and personnel for adherence to all cGMP, SOP’s and safety regulations. | 2/28/2019 |
| 15918 | Nephron Pharmaceuticals West Columbia, SC Micro Analyst I BS in biology or related life sciences Exp: 1+ years |
Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Apply quality scientific techniques in the microbiological analysis of raw materials; in-process & finished product samples to include: sterility, bioburden, identification, environmental monitoring, growth promotion, microbial recovery and media fill tests following approved procedures. Demonstrate ability to understand and interpret test results in relation to acceptance or rejection of lot tested. Report, initiate documentation and assist in excursions and investigations of OOS and OOT reports. | 2/28/2019 |
| 15919 | NeuroPace Mountain View , CA Manufacturing Engineer BS in mechanical or industrial engineering Exp: 0-4 years |
Maintain quality standards in and around manufacturing areas, ensuring a safe work environment for all personnel and helps to develop a culture of accountability, continuous improvement, and collaboration. Responsibilities includes: Write, review, and improve manufacturing procedures and forms in compliance with the quality system, ensuring accuracy and consistency. Collaborate with Manufacturing and Development Engineers to create, review, and maintain manufacturing routers. Including verifying manufacturing labor times are properly calculated. Support departmental responsibilities associated with training and qualifying manufacturing assemblers. | 2/28/2019 |
| 15920 | NGM Biopharmaceuticals South San Fransico, CA Research Associate I BS in life sciences Exp: 0-2 years |
he primary responsibilities will include planning and execution of experiments focused on novel target discovery and validation using a wide range cutting edge in vitro and in vivo techniques. The new team member is expected to work within a cross-functional team generating high quality biological data fueling NGM’s drug discovery engine. Design and execute experiments for target identification and validation including utilization of in vitro cell-based assays and in vivo disease animal models. | 2/28/2019 |
| 15921 | Avecia Milford, MA Research Associate MS in chemistry or life sciences Exp: 1+ years |
The Research Scientist I is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. Provide technical leadership in analytical project meetings. Communicate with clients and contributes to department objectives for continuous improvement and technical excellence. | 2/28/2019 |
| 15922 | Nkarta South San Fransico, CA Research Associate/Senior/Process Engineer MS in biology related discipline Exp: 1-6 years |
Job duties and responsibilities include: support process development of phase appropriate cell therapy production processes. Evaluate raw materials and culture systems for use in cell therapy manufacturing processes. Support process optimization efforts to increase process robustness, reduce costs and improve yield. Design and execute experiments independently; accurately record, analyze and communicate data to senior staff and team members. | 2/28/2019 |
| 15923 | Nordson Sunnyvale, CA Manufacturing Engineer I, Nordson MEDICAL BS/BA in mechanical engineering Exp: 1-2 years |
This individual will possess a broad range of medical device manufacturing engineering skills and experience, as well as depth of knowledge with assembly processes, equipment, and tooling. The ideal candidate is a self-motivated individual who is comfortable rolling up their sleeves and working hands-on in the process. Job duties include: Develop R&D pilot lines for new products and ensure design for manufacturability (DFM) through concurrent engineering practices. Establish robust assembly processes for both new products developed at Nordson Medical and those transferred into Nordson Medical. | 2/28/2019 |
| 15924 | Nordson Amherst, OH Test Engineer (Electrical) BS in electrical or computer engineering Exp: 0-2 years |
Job duties and responsibilities include: Electrical and mechanical aptitude with the ability to design, fabricate and wire electrical control panels and test fixtures. Write comprehensive documentation on tester hardware and software designs. Provide troubleshooting support to engineering and assembly teams on products and processes | 2/28/2019 |
| 15925 | Nordson Amherst, OH Process/ Product Support Engineer BS in mechanical or electrical engineering Exp: 1-3 years |
Responsible for supporting both pre-sales and post-sales activities including customer process development, product engineering and demonstrations, material evaluation, on-site installation, servicing and repair of complex equipment and systems for all products and markets. Also serves as company liaison with customers on administrative and technical matters and be assigned to specific customer accounts as the primary technical support contact. | 2/28/2019 |
| 15926 | Nordson Concord, CA Associate Engineer, Mechanical BS/BA Exp: 0-2 years |
Responsible for designing, defining, implementing system requirements, analyzing and/or testing Asymtek products. Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained. Receives specific and detailed instructions as to required activities and expected results. Performs a variety of routine tasks, which should provide experience and familiarization with the engineering staff, methods, practices and programs of the company. | 2/28/2019 |
| 15927 | Norwich Pharma Norwich , NY Chemist I BS in chemistry, biology, or related Exp: 0-3 years |
Duties and functions include: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. | 2/28/2019 |
| 15928 | Idex Corporation Irvine, CA Mechanical Engineer BS/BA in engineering Exp: 1 year |
Responsible for mechanical design, including new product development, research and development, conceptual design, detail design, testing, validation and design for manufacture of specialized fluid handling and management systems. Duties include evaluating, quoting and releasing modifications of these existing product lines, supporting production, evaluating and process engineering changes, cost reductions and product improvement projects. | 2/27/2019 |
| 15929 | Micropoint Bioscience Santa Clara, CA Quality Control Associates MS in chemistry, biology or related Exp: 0-2 years |
(Two openings) These positions are responsible for participating as team members in a laboratory environment for finished product/or development programs focused on the goal of testing and releasing the immunoassays found in Micropoint's in-vitro diagnostic products for point-of-care (POC) testing. Responsibilities include: Work with QA/QC manager to test, characterize and release quantitative immunoassays to meet both FDA and EU regulatory requirements for diagnostic IVD applications, Assist the R&D team in the POC product development including feasibility, verification and validation, manufacturing transfer and commercialization | 2/27/2019 |
| 15930 | Micropoint Bioscience Santa Clara, CA Manufacturing Operators HS Diploma Exp: 0-2 years in manufacturing |
(Two openings)These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the company's disposable test cartridges. Responsibilities include: Follow written procedures for set-up, operation, and clean up of manufacturing equipments, final assembly, and packaging, Responsible for manual tasks including, pipette solution, pouch and box labeling, product inspection, Maintains records and documentation associated with producing cartridges in compliance with GMP and SOPs | 2/27/2019 |
| 15931 | MicroVention Terumo Aliso Viejo, CA Engineer I/Engineer II BS in engineering or chemistry Exp: 0-2 years |
This 24-month rotational program is designed to train new Engineers on various aspects of MicroVention - Terumo technology, procedures, and processes. All candidates will be assigned a Mentor, as well as an Advisor to oversee their program succession, and will be provided with additional classroom training. Successful candidates will have three (3) eight-month rotations. These rotations include one (1) required rotation and two (2) optional rotation. The Engineer I (EIT) supports development of medical device products with work including writing or verifying specifications, designing new products, fixtures, test processes, equipment and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Typical job duties might include: Developing new product concepts and products. Engineering design and process development. Generating intellectual property and writing invention disclosures.This 24-month rotational program is designed to train new Engineers on various aspects of MicroVention - Terumo technology, procedures, and processes. All candidates will be assigned a Mentor, as well as an Advisor to oversee their program succession, and will be provided with additional classroom training. Successful candidates will have three (3) eight-month rotations. These rotations include one (1) required rotation and two (2) optional rotation. The Engineer I (EIT) supports development of medical device products with work including writing or verifying specifications, designing new products, fixtures, test processes, equipment and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Typical job duties might inc | 2/27/2019 |
| 15932 | MicroVention Terumo Alajuela , Co Engineer JR BSChe, ME, EE, IE degree Exp: 1 year |
Duties and functions include: Improve, sustain, develop, and support of new and existing manufacturing processes for new and existing products, product changes and enhancements, as well as related tooling and fixtures. Investigation and testing of product processes. Manages builds for new product development in prototype and pilot production setting, including training of operators and coordination with production planning | 2/27/2019 |
| 15933 | MicroVention Terumo Aliso Viejo, CA Regulatory Affairs Associate BS/BA degree Exp: 1-3 years |
The Regulatory Affairs Associate/Regulatory Affairs Specialist is in a high-visibility, high-recognition role and will be responsible for obtaining regulatory approvals, and ensures compliance to China-specific regulatory agency requirements. Job duties: Executes regulatory requirements for China. Reviews and files worldwide regulatory submissions (dossiers/ technical files / STED) to ensure MicroVention devices are commercially available in international markets based on the organization’s objectives. Reviews and files China submissions (JV & MV). Communicates with regulatory agencies on administrative and routine matters. | 2/27/2019 |
| 15934 | MICR Indianapolis, IN Medical Research Study Coordinator: BS/BA and/or CCRC certification Exp: 1-3 years |
We are seeking an experienced individual who has coordinated the implementation of clinical research protocols. 1-3 years of clinical research experience and CCRC certification is preferred for this full-time position. | 2/27/2019 |
| 15935 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, biology or related Exp: 0.5-1 years |
Essential job functions include: Safely perform operations to meet quality expectations. Ensure quality throughout the process. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). Ensure all applicable log books have been filled out completely as required by current procedures. In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. | 2/27/2019 |
| 15936 | Merck KGaA Rocklin, CA Associate Scientist BS/BA in life sciences Exp: 1+ years |
Essential job functions include: Performs IHC, ELISA, and any other relevant tests as needed to conduct product development testing. Assists with establishing, maintaining, and updating the Design History Files (DHF) for new and/or existing products. Performs published literature reviews. Identifies and documents published clones, published protocols, etc as required.Provides technical support on developing new and improving existing IHC reagent processes and products. Conducts organized development testing to generate support data for new potential products or changes to current products. | 2/27/2019 |
| 15937 | Merck KGaA Rockville, MD Lab Technician Analytical Chemistry/Formulations HS Diploma Exp: 1+ years |
At MilliporeSigma the Lab technician will perform a variety of tasks to support the laboratory technical staff who are required to characterize a product or material, dose formulation or bio-analytical sample for concentration, stability or other characteristics. The Lab technician will perform tasks as needed to maintain the lab and to support the assays performed in the Analytical Chemistry and Formulation labs. | 2/27/2019 |
| 15938 | Merck KGaA Miamisburg, OH Production Associate AS or BS/BA in scientific field Exp: 6+ months |
Evaluate stable isotope products according to established protocols, provide technical support to others and perform operations in support of the group and department. Essential job functions include: Perform multi-disciplined, established assays and/or unit operations, involving stable isotope compounds. Ensure all applicable log books have been filled out completely as required by current procedures. Perform routine troubleshooting and miscellaneous duties or tasks as necessary. In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. | 2/27/2019 |
| 15939 | Miltenyi Biotech Sunnyvale, CA Manufacturing Associate BS in biological sciences or related Exp: 1-3 years in GMP environemtn or equivalent |
The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. | 2/27/2019 |
| 15940 | Mission Pharmacal San Antonio, TX Product Assistant BS/BA degree Exp: 0-1 years |
Provide support managing the Samples and Marketing Materials for the Mission salesforce teams. Assist with coordinating shipment orders with the Distribution Centers on a weekly basis. Coordinate and maintain items in Sales force Ordering system on daily basis. Maintain the Sales Incentive reward program for the sales force. Provide sales reports for samples and marketing materials to the marketing teams and Outside Marketing Resources, when requested, usually monthly. Provide Sales Reports to Department Supervisor when necessary. Maintain inventory of samples and training materials for the new hire training. On a quarterly basis, pack and ship new hire training materials to and from the training location, as required. | 2/27/2019 |
| 15941 | moderna Cambridge, MA (Contract) Research Associate, Formulation Design BS or MS Exp: 0-3 years in formulation or drug delivery |
This position is seeking a contract Research Associate/Sr. Research Associate who will be responsible for preparation and characterization of mRNA formulations within a dynamic and highly interdisciplinary environment. Understanding of nanoparticle preparation techniques and biophysical / chemical characterization is essential for this position. Experience with nucleic acid delivery systems is a plus. He/she will be responsible for executing lab experiments, reporting results, performing stability assessments, maintaining a high-quality lab notebook and working within a larger team of formulation scientists and associates. The successful candidate must have a foundation in pharmaceutical sciences and materials science/engineering. | 2/27/2019 |
| 15942 | moderna Norwood, MA (Contract) Associate II, Quality Control BS/BA in scientific discipline Exp: 0-2 years lab experience |
The individual in this role will perform cGMP QC testing for QC Chemistry, release and stability. Also, this individual may support special projects as assigned. The shift for this role will be a 4 days a week for 10 hours a day (4X10) on either Sunday-Wednesday or Wednesday -Saturday. | 2/27/2019 |
| 15943 | mpbio Solon, OH QC Technician HS Diploma Exp: 0 years |
The QC Technician is responsible for a wide variety of routine tasks in the Quality Control Department. These include: RIA and EIA bench top assay work. Inspection of incoming raw materials. Refrigerator and freezer temperature monitoring. QC document copying, collating, and filing. | 2/27/2019 |
| 15944 | Charles River Spencerville, OH Formulations Technician I AA/AS or BS/BA in life sciences or related Exp: 0-1 years |
The Formulations Technician will prepare routine test article/substance dosage solutions and/or suspensions in accordance with Standard Operating Procedure (SOP) and Good Laboratory Practice (GLP) guidelines under direct supervision, and may serve as primary technician on studies that tend to be routine, less complex studies. In a typical day, you will perform standardized preparation procedures and calculations, ensure record keeping is consistent and correct, complete documentation for the use of all test articles and vehicles/reagents to ensure consistency and correctness, and receive incoming test articles/substances and reagents. You will also be expected to ensure formulations samples are collected, packaged, and shipped properly and on time, as well as ensure the test articles from assigned completed studies are returned to the sponsor or reassigned to another protocol. Additionally, you will respond to Quality Assurance (QA) audits of preparation procedures and calculations on assigned studies, ensure data sheets are complete and submit them for review, assist in reviewing data, prepare labels and samples, maintain cleanliness and general appearance of the laboratory, ensure the laboratory is stocked and assist in maintaining current inventory of reagents, test articles, vehicles, and samples, utilize appropriate Quality Control (QC) procedures/measures to help verify the accuracy and correctness of data prior to submission to internal QA, and perform all other related duties as assigned. | 2/27/2019 |
| 15945 | Charles River South San Fransico, CA Research Associate BS/BA Exp: 0-3 years lab experience |
This position will be involved in all aspects of studies supporting the bioanalysis of drug molecules in multiple matrices. The position is hands-on, working in close cooperation with and under the guidance of more senior staff members in a fast-paced environment where a commitment to teamwork, quality data and speed is essential. | 2/27/2019 |
| 15946 | Charles River Shrewbury, MA Research Technician I HS Diploma or BS in animal/life sciences Exp: 0.5-1 years in research |
The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 2/27/2019 |
| 15947 | Charles River Mattawan, MI Research Technician - Reproductive Toxicology - T-Lab HS Dipolma or BA/BS or MS Exp: 0 years |
A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 2/27/2019 |
| 15948 | Charles River Shrewsbury, MA Research Technician I HS Diploma or BS in animal/life sciences Exp: 0.5-1 years in research |
The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 2/27/2019 |
| 15949 | Charles River Spencerville, OH Research Technician HS Diploma or BS in animal/life sciences Exp: 0.5-1 years in research |
The Research Technician will collect and record data with minimal supervision in the performance of studies. During a typical day, you can expect to perform clinical observations, sample collection, monitoring of food consumption, animal husbandry, and accurate data collection and reporting, along with the handling and restraint of animals. Additionally, you will also administer test substances by various basic methods, perform study preparation activities, read basic study protocols and extract pertinent information, review documentation of performed functions, maintain a clean work area, receive animals of all species (general health observation, sexing and identification), and perform all job functions using Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), processes, and company policies. | 2/27/2019 |
| 15950 | MyoKardia South San Fransico, CA Research Associate I - Cell biology BS in physiology, pharmacology or related Exp: 1-2 years animal handling |
Essential duties and responsibilities include: Prepare isolated adult animal cardiomyocytes for contractility assays, Use pre-established experimental designs to plan, and execute myocyte contractility and Ca2+ transient assays, Propose solutions to technical issues: proactively seek out senior team member to discuss potential resolutions to problems | 2/27/2019 |
| 15951 | MyoKardia South San Fransico, CA Research Associate I - Biology BS in biochemistry, biology or related Exp: 0-2 years |
Essential duties and responsibilities include: Purification of a wide variety of cardiac muscle proteins using various chromatographic techniques, Carry out multiple experiments in parallel and keep detailed, meticulous notes, Analyze and report experimental results, both in daily updates, regular database inputs, and in final reports, Execute all methods and techniques required to purify soluble and secreted proteins including the ӒKTA PURE FPLC platform, SDS-PAGE, TFF, microfluidizer, plate-based assays, spectrophotometry, and HPLC | 2/27/2019 |
| 15952 | Myriad Genetic Laboratories Salt Lake City, UT Patient Advocate Triage I BS/BA in biology, science, or healthcare Exp: 1-2 years |
Triage Patient Advocate reviews all paperwork submitted with patient samples to ensure all required information for testing is received. They enter the patient’s insurance information into the database application and determine if the patient’s insurance requires additional documentation/processing for testing to be covered. The ability to focus on quality is crucial in this role. The candidate must be very detail oriented as well as be able to determine how small details will affect case completeness as a whole. | 2/27/2019 |
| 15953 | NanoString Seattle, WA Automation Engineer I BS in engineering, science, or biology Exp: 1+ years |
The Automation Engineer I is responsible for maintaining existing Manufacturing systems as required. Additional duties include the development of new methods and implementation of new systems. The ideal candidate has knowledge of FDA and ISO requirements as they apply to manufacturing processes.The Automation Engineer I is responsible for maintaining existing Manufacturing systems as required. Additional duties include the development of new methods and implementation of new systems. The ideal candidate has knowledge of FDA and ISO requirements as they apply to manufacturing processes.The Automation Engineer I is responsible for maintaining existing Manufacturing systems as required. Additional duties include the development of new methods and implementation of new systems. The ideal candidate has knowledge of FDA and ISO requirements as they apply to manufacturing processes. | 2/27/2019 |
| 15954 | NanoString Seattle, WA Manufacturing Research Associate I (Tuesday thru Saturday)-CodeSet Production BS in scientific discipline Exp: 0-2 years lab experience |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 2/27/2019 |
| 15955 | NanoString Seattle, WA Manufacturing Research Associate I (Monday thru Friday) -Consumables Production BS in scientific discipline Exp: 0-2 years lab experience |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 2/27/2019 |
| 15956 | NanoString Seattle, WA Manufacturing Research Associate I (Mon thru Fri)-CodeSet Production BS in scientific discipline Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 2/27/2019 |
| 15957 | Merck Elkton, VA Associate Specialist Engineering, Bulk Manufacturing BS in engineering Exp: 0.5-1 years |
The role encompasses technical services support in the areas of equipment and automation systems, validation, deviation management and product franchise. Specific assignments may be focused in one area or span across multiple areas of focus. Candidates will be responsible for: Provide on-the-floor support of operational and technical issues; collaborating with the shop floor to provide immediate responses to deviations and potential deviations. Performing deviation investigations aimed to prevent deviation re-occurrence, including determining the root cause, identifying corrective/preventative actions, identifying event scope, and conducting a product impact assessment. Where applicable, complete investigational test protocols to determine root cause, product impact, event scope, etc | 2/22/2019 |
| 15958 | Merck West Point, PA Scientist/Engineer, Bio-Process Development MS in chemical engineering or biological sciences Exp: 1+ year |
The primary job responsibility will be to deliver on specific assigned objectives related to development of robust and scalable processes for the manufacture of clinical supplies and subsequent technical transfer of such processes to GMP operations. The successful candidate will have a strong working knowledge of chromatography, membrane filtration, and centrifugation technologies and be able to apply this understand towards process development challenges. Experience in programming (e.g. Visual Basic, Python) and statistical & data visualization software (e.g. Excel, Spotfire, JMP, Design Expert) will be considered as a positive factors. In addition to the core responsibilities outlined above, the individual is expected to have an understanding of the regulatory guidelines governing cGMP manufacture, keep careful notes, comply with all required training, and maintain a focused attention on laboratory safety. | 2/22/2019 |
| 15959 | Merck Durham, NC Process Engineer – Merck Manufacturing Division BS in engineering or sciences Exp: 0 years |
The successful candidate will be expected to be a first responder to requests from the manufacturing areas when support is needed. The well-qualified candidate must have analytical, problem-solving, and communication skills. In this role, the candidate will provide support for the manufacturing of aseptic products. | 2/22/2019 |
| 15960 | Merck West Point, PA BS/BA Exp: 1+ years internship/coop experience |
This individual will be involved in streamlining and optimizing system operations while working with the Command Center System Engineer. The Operations Support Engineer will also be heavily involved in troubleshooting and resolving issues related to systems and programs used in the Commend Center. This role is highly visible and will need to work very efficiently with other departments on the plant site, as well as, contract personnel and external agencies. This is a multi-tasking position and requires strong attention to detail. Develops and maintains comprehensive knowledge of West Point facilities, operations, and personnel. Utilizes available resources to ensure continuous smooth operation of the site. | 2/22/2019 |
| 15961 | Meridian Cincinnati, OH Lot Release Associate I BS in biology or related Exp: 0-1 years |
The Lot Release Associate I is responsible for ensuring product quality assurance requirements are satisfied and fully documented. They will participate in the review of quality documentation, review of production and documentation, and any other associated activities to ensure product compliance prior to release of product. Responsibilities include: Maintain departmental trend information. Set up, completed and maintain all Lot Release log sheets. Ensure that all Lot Release records are appropriately stores, maintained and retrievable. etc | 2/22/2019 |
| 15962 | Meridian Research Bradenton, FL Clinical Research Coordinator AA/AS or higher Exp: 0-2 years |
Responsibilities and Duties include: Coordinate Clinical Studies adhering to the principles of Good Clinical Practice Collect initial medical background from patients and other appropriate sources Work as a cohesive team member coordinating assigned studies and backing up other studies on location Educate and provide information to patients, families, and community groups regarding clinical drug trials Assist and support Recruitment Team with prescreen activities and other activities related to subject recruitment | 2/22/2019 |
| 15963 | Merieux NutriSciences Madison, WI Microbiologist BS/BA Exp: 1-2 years |
The incumbent is responsible for the testing of food samples using various microbiological analyses. Job responsibilities include: Follow appropriate methods and SOPS when conducting sample preparation. Maintain quality control records. Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Perform confirmation tests on suspect plates or tubes to identify the strain of bacteria. | 2/22/2019 |
| 15964 | Merit Medica South Jordan, UT Product Manager I BS/BA in marketing or related Exp: 1+ years |
Responsible for providing routine product marketing and analysis support. Essential functions include: Works with product users to increase the ability of Merit to improve products to meet specific customer needs, Works with customers in coordinating Market Research Trials, Evaluates new product potential, Serves on product decision making teams to assist in product development and identifying marketing opportunities, etc. | 2/22/2019 |
| 15965 | Merit Medica Malvern, PA R&D Engineer II MS in science or engineering Exp: 1+ years |
Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision and guidelines. Essential duties include: Independently evaluates, selects, and applies standard technical techniques, procedures, and criteria, using judgement in making minor adaptations and modifications. Investigates a moderate number of technical variables in completing assignments that have clear and defined objectives. Performs work which involves conventional types of plans, investigations, surveys, structures, or equipment with relatively few complex features for which there are precedents. | 2/22/2019 |
| 15966 | Merit Medica Malvern, PA R&D Engineer BS/BA or MS in engineering or sciences Exp: 0-1 years |
Performs routine technical work such as the design, manufacture and operation of structures, machines and systems under general supervision and guidelines. Essential duties include: Performs routine technical work requiring the application of standard techniques, procedures, and criteria in carrying out engineering tasks, uses limited amounts of discretionary judgment in making decisions regarding technical alternatives, performs work of some higher technical level for training purposes, and work is screened to ensure correct application of scientific principles. | 2/22/2019 |
| 15967 | Merit Medica South Jordan, UT Manufacturing Lab Engineer I BS/BA or MS in mechanical or manufacturing engineering Exp: 0-2 years |
Our Manufacturing Lab Engineer performs testing on equipment and parts in a manufacturing lab environment. Performs routine technical work such as the design, manufacture and operation of structures, machines and systems under general supervision and guidelines. Prepares and tests specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Performs routine technical work requiring the application of standard techniques, procedures, and criteria in carrying out engineering tasks. | 2/22/2019 |
| 15968 | Merit Medica Malvern, PA Quality Assurance Inspector - 1st Shift HS Diploma Exp: 6 months |
This position operates, maintains and troubleshoots clippers, stretchers, and testing equipment. Operations are performed per written SOPs, including CGMP guidelines. Perform inspection of extruded products such as braided shafts, non-braided tubes, tips, etc. Completes the inspection steps of clipping and stretching to ensure smooth product flow. Complete paperwork associated with work orders being processed. Interacts with material handling for checking orders into stock. | 2/22/2019 |
| 15969 | Merz Mesa, AZ Regulatory Affrs Assoc BS/BA in scientific or healthcare discipline Exp: 1+ years |
The Regulatory Affairs Associate supports the regulatory activities for development projects including new products and life cycle management. This includes assisting with regulatory strategies and timelines as well as the development and implementation of submissions under the direction of a line manager. With support from Regulatory Affairs Manager, provide ongoing support to cross functional teams to provide regulatory strategies during product development. Support preparation and coordination of submissions in accordance with the current regulations and guidance’s. Ensure submissions support company objectives and strategy. Identify and communicate regulatory risks and project issues. Make recommendations to team and regulatory management. | 2/22/2019 |
| 15970 | Method Sense Marrisville, NC Quality Assurance Associate BS Exp: 1-3 years |
We are seeking a Quality Assurance Associate to work closely with the MethodSense Executive Team and Project Managers to assist with the maintenance of client’s Quality Management Systems, supporting client Regulatory solutions, and the implementation and maintenance of client technology solutions on a contract basis. | 2/22/2019 |
| 15971 | MQA Concord, CA Microbiology Lab Tech I AS in biology or related Exp: 0-1 years |
The lab tech performs or supports testing such as microbial load estimation by different methods, MIC, MBC, disinfectant studies, antimicrobial assays, bacteria and mold identification, PCR, water chemical analysis, endotoxin test, virology assays, SDS PAGE, BCA, Cytotoxicity assays, cell banks and collects air, surface and water samples at MQA or client facilities. Testing is performed in accordance with standard operating procedures. Monitors and checks operation, calibration, and service condition of laboratory equipment along with monitoring and maintaining laboratory supplies. Complies with procedures and adhere to documentation practices in accordance with MQA policies. Perform data entries into computer databases, along with reporting adverse or unusual events to management. Participates in process improvement activities as needed. Prepare SOPs as needed. | 2/22/2019 |
| 15972 | American Regent New Albany , OH R&D Analytical Chemist I BS in chemistry Exp: 1+ years |
This R&D position will be responsible for testing of raw materials, finished products, and stability samples using existing analytical methods and wet chemistry. Perform routine analytical testing of raw materials, finished product, stability samples and lab batch samples. Record and report all lab data as per approved procedures and regulatory requirements. | 2/21/2019 |
| 15973 | Luminex Associate Scientist II, IL ASSOCIATE SCIENTIST II BS/BA in science, chemistry or biomedical sciences Exp: 1-3 years |
Manufacturing oligonucleotides used in Luminex’s diagnostic tests. (The oligonucleotides are used to prepare a variety of chemical reagents that are filled into assay consumables such as trays or cartridges). The oligonucleotide manufacturing process is a manual, multi-step wet chemistry process. The operation of specialized computer controlled instrumentation such as synthesizers and purification equipment used in the manufacture of defined sequence oligonucleotides. | 2/21/2019 |
| 15974 | United Therapeutics Research Triangle Park, NC Research Associate - Tissue Engineering BS/BA or MA in science, engineering or biological sciences Exp: 1-2 years |
Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. Prepare lung scaffolds for tissue engineering experiments, cannulate and load scaffolds into bioreactor chambers, and seed scaffolds with pulmonary cells. Perform maintenance, cleaning, sterilization, and set-up of bioreactors for tissue engineering studies. Follow proper procedures regarding laboratory safety, use of personal protective equipment, and handling of biohazard materials, including human or animal cells and tissues Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. Prepare lung scaffolds for tissue engineering experiments, cannulate and load scaffolds into bioreactor chambers, and seed scaffolds with pulmonary cells. Perform maintenance, cleaning, sterilization, and set-up of bioreactors for tissue engineering studies. Follow proper procedures regarding laboratory safety, use of personal protective equipment, and handling of biohazard materials, including human or animal cells and tissues Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. Prepare lung scaffolds for tissue engineering experiments, cannulate and load scaffolds into bioreactor chambers, and seed scaffolds with pulmonary cells. Perform maintenance, cleaning, sterilization, and set-up of bioreactors for tissue engineering studies. Follow proper procedures regarding laboratory safety, use of personal protective equipment, and handling of biohazard materials, including human or animal cells and tissues | 2/21/2019 |
| 15975 | LSNE Madison, WI QC Microbiology Technician BS Exp: 0-2 years |
Job summary: Conducts sampling of incoming raw materials, production environments, and/or facility clean utilities, as per approved procedures and submits these samples to the appropriate testing facility for documented and controlled results. Applies material / system status labels, as indicative of testing status and/or results obtained. Assists with lab maintenance and inventory. | 2/21/2019 |
| 15976 | Machaon Diagnostics Oakland, CA Clinical Laboratory Assistant BS/BA in chemistry, biology, or related Exp: 6 months |
Demonstrate proficiency and understanding of standard clinical laboratory practices. Review requisitions, orders tests and processes specimens in preparation for laboratory procedures. Perform general laboratory maintenance tasks including preparing reagents, re-stocking consumables and washing glassware. Assist with quality control and quality assurance paperwork. Assist with clinical trials including completion of Institutional Review Board documentation, subject recruitment, screening, and management, and performance of research related testing. Design and revise forms and protocols. Adhere to Machaon policies and procedures as directed by the supervisor, manager or medical director. Interact with patients, subjects, visitors, physicians, and coworkers in a professional and courteous manner. | 2/21/2019 |
| 15977 | Mammoth Biosciences San Francisco, CA Resaerch Associate BS/BA in chemistry, biology, or related Exp: 1+ years |
Mammoth is seeking a Research Associate experienced in protein and nucleic acid biochemistry techniques to work with our CRISPR development team. The ideal candidate will have experience with protein engineering, molecular biology, protein purification and bioinformatics. Further, the candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. The Research Technician will report directly to a Scientist. | 2/21/2019 |
| 15978 | Manus Bio Cambridge, MA Research Assistant, Molecular Biology BS or MS in bioengineering, biology, or biochemistry Exp: 1+ years lab experience |
Responsibilities include but are not limited to: Construct and validate gene and plasmid constructs, Express metabolic pathways in microbial systems, Test expression and activity of enzymes in a variety of assays, Ferment bacterial cultures, Perform analytical assays to identify and quantify metabolites | 2/21/2019 |
| 15979 | Masy Bioservices Pepperell, MA Inventory Technician I HS Diploma Exp: 1-2 years |
This position is responsible for ensuring all incoming customer product is correctly inspected, inventoried and accurately entered into the electronic inventory system. This includes initially entering data and being a secondary reviewer. Duties include abiding by area work instructions and ensuring that customer product is stored at appropriate conditions during inventory to ensure compliance. Communicate with appropriate personnel to determine all pertinent information that needs to be captured | 2/21/2019 |
| 15980 | MedImmune Gaithersburg, MA Researc Associate MS Exp: 1-2 years lab experience |
his is a hands-on laboratory-based position to support pre-clinical research to further our understanding of the disease-driving mechanisms and to develop new medicines for respiratory diseases such as COPD, asthma, and pulmonary fibrosis. The candidate will assist in study design, execution and data analysis of complex and technically demanding in vitro and in vivo experiments using a variety of cellular and molecular techniques. The candidate will develop close working relationships within a highly collaborative environment using strong interpersonal and communication skills to advance team goals. his is a hands-on laboratory-based position to support pre-clinical research to further our understanding of the disease-driving mechanisms and to develop new medicines for respiratory diseases such as COPD, asthma, and pulmonary fibrosis. The candidate will assist in study design, execution and data analysis of complex and technically demanding in vitro and in vivo experiments using a variety of cellular and molecular techniques. The candidate will develop close working relationships within a highly collaborative environment using strong interpersonal and communication skills to advance team goals. | 2/21/2019 |
| 15981 | MedImmune Gaithersburg, MA Rsearch Associate II MS in biology or related Exp: 0-2 years |
Major responsibilities include planning and executing experiments related to developing protein engineering platforms for therapeutic antibody generation and optimization. She/he will work with scientists to create research plans, execute experiments, analyze and interpret data and present results to the group and the department. She/he is expected to have a strong work ethic, excellent organizational skills and keep good records. Strong team-based communication and presentation skills will be required. | 2/21/2019 |
| 15982 | MedImmune Gaithersburg, MA R&D Associate II - BPD MS in mechanical or biomedical engineering Exp: 0-2 years |
This role will contribute in the development of product requirements, generate and evaluate device concepts, conduct engineering analyses, develop detailed engineering specifications, create device designs, and perform design verification/validation testing in a cross-functional team to ensure successful development and launch of mechanical and electro-mechanical medical devices. This role requires excellent technical writing skills and good understanding of design control process. | 2/21/2019 |
| 15983 | MedImmune Gaithersburg, MA Engineer I/II BS or MS Exp: BS: 0-2 years for Engineer I, MS: 1+ years for Engineer II |
This position reports to the Associate Director of Engineering Technical Services supporting GMP clinical biomanufacturing. Responsible for maintaining reliable equipment performance for one or more manufacturing systems at MedImmune’s Gaithersburg Clinical Manufacturing facilities including cell culture, purification, and support systems. Monitors equipment performance. Identifies equipment issues and develops technical solutions | 2/21/2019 |
| 15984 | MedImmune Gaithersburg, MA R&D Associate II MS in biology or related Exp: 0-2 years |
The successful candidate will carry out bioanalytical cell based assay testing of recombinant protein therapeutics under cGMP. The ideal candidate will make detailed observations, analyze data, interpret results, and exercise appropriate technical discretion in the design, execution, and interpretation of experiments in an independent manner.This person may be involved in the qualification and validation of cell-based bioassays for biological characterization and testing of biopharmaceutical products, and assist in assay investigations and troubleshooting. He/She will perform cell culture, maintain cell lines and perform routine lab equipment maintenance. The candidate will be expected to prepare technical reports, SOPs and technical summaries for meeting presentation. The candidate will be expected to assist/lead investigation for non-conformances and coordinate equipment validation with different departments. | 2/21/2019 |
| 15985 | Medpace Cinncinnati, OH Vender Management Associate BS/BA Exp: 1+ years |
Review third party contracts for business implications and acceptable predefined legal terms; Utilize governance, risk, and compliance (GRC) software to contribute to contract management and third party information; Employ risk analysis processes in the performance of third party due diligence; Apply understanding of policies and procedures associated with purchase contracts such as indemnification and amendments; Review third party performance ensuring that contract KPI’s are achieved and develop relevant improvement plans in collaboration with the operations teams; Analyze financials to assist in negotiation of agreements; Prepare and coordinate third party requests for proposals; and May be responsible for other projects and responsibilities as assigned. Review third party contracts for business implications and acceptable predefined legal terms; Utilize governance, risk, and compliance (GRC) software to contribute to contract management and third party information; Employ risk analysis processes in the performance of third party due diligence; Apply understanding of policies and procedures associated with purchase contracts such as indemnification and amendments; Review third party performance ensuring that contract KPI’s are achieved and develop relevant improvement plans in collaboration with the operations teams; Analyze financials to assist in negotiation of agreements; Prepare and coordinate third party requests for proposals; and May be responsible for other projects and responsibilities as assigned. | 2/21/2019 |
| 15986 | Viant Orchard Park, NY Design Engineer BS/BA in related field Exp: 0-3 years |
Initiates, directs and manages the design, development, constructing and modification of products and processes from conception to implementation. Works closely with other departments to coordinate design engineering activities. Reviews, initiates or approves engineering drawings, layouts, changes orders and specifications. | 2/21/2019 |
| 15987 | Medtronic Miami Lakes, FL Associate Supplier Quality Engineer BS/BA in engineering or sciences Exp: 0 years |
Responsibilities may include the following and other duties may be assigned. Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness.Responsibilities may include the following and other duties may be assigned. Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. | 2/21/2019 |
| 15988 | Medtronic Davers, MA Associate Microbiologist BS/BA or MS in biology, biomedical engineering, or technical discipline Exp: 0 years |
Reviews sterile load cycle data and performs sterile load release for finished product lots manufactured by Medtronic Danvers or contract manufacturers. Administers the Environmental Monitoring Program for the Danvers manufacturing areas including viable and non-viable particulate counts, product bio-burden, water and surface microbial levels, etc. to ensure an appropriately controlled environment meeting regulatory expectations and industry standards. Communicates detailed information regarding monitoring results and trends to Manufacturing and Quality; recommends revisions to monitoring program and/or manufacturing process controls and ensures effective corrective actions are implemented, where necessary. | 2/21/2019 |
| 15989 | Medtronic Boulder , CO Associate R&D Engineer BS/BA in engineering or sciences Exp: 0 years |
Responsibilities may include the following and other duties may be assigned. • Works as part of a team, providing technical support on New Product Development and Sustaining Project Initiatives, ensuring medical devices are designed with the utmost regards to safety, reliability and quality. • Designs, develops, analyzes, troubleshoots and provides technical skills during legacy product remediation and new product development. • May be involved in product research and development, including assessing user needs and product requirements • Reviews existing and generates new Technical Documentation to ensure Medical Devices comply with all applicable standards. Includes generating and executing verification test protocols. • Translates research discoveries into usable and marketable products.Responsibilities may include the following and other duties may be assigned. • Works as part of a team, providing technical support on New Product Development and Sustaining Project Initiatives, ensuring medical devices are designed with the utmost regards to safety, reliability and quality. • Designs, develops, analyzes, troubleshoots and provides technical skills during legacy product remediation and new product development. • May be involved in product research and development, including assessing user needs and product requirements • Reviews existing and generates new Technical Documentation to ensure Medical Devices comply with all applicable standards. Includes generating and executing verification test protocols. • Translates research discoveries into usable and marketable products. | 2/21/2019 |
| 15990 | Medtronic North Haven, CT Quality Engineer - Manufacutring Operations MS in engineering or sciences Exp: 0 years |
esponsibilities may include the following and other duties may be assigned. Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. Collaborates with engineering and manufacturing functions to ensure quality standards are in place. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements. May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality. Provide Quality Engineering support as a Process Validation team member and lead/execute Test Method Validations and Measurement Systems Analysis (MSA).esponsibilities may include the following and other duties may be assigned. Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. Collaborates with engineering and manufacturing functions to ensure quality standards are in place. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements. May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality. Provide Quality Engineering support as a Process Validation team member and lead/execute Test Method Valida | 2/21/2019 |
| 15991 | LabCorp New York, NY Specimen Processing Specialist (Laboratory Associate) HS Diploma Exp: 1+ years lab experience |
Prepares laboratory specimens for analysis and testing. Spinning samples, pouring urine tubes and creating frozen samples. Picking up and delivering samples to clients/hospitals. Unpacks and routes specimens to their respective staging areas. Accurately Identify and label specimens. Pack and ship specimens to proper testing facilities. | 2/20/2019 |
| 15992 | LabCorp Phoenix, AZ Lab Assistant HS Diploma Exp: 1-2 years |
Performs all paperwork, technical, and non-technical procedures required to process and submit specimens. Assigns specific computer generated identification numbers, checks for accuracy, and records all items processed. Forwards accessioned specimens to designated laboratory location(s); and locating and correcting any discrepancies. Learns and keeps familiar with lab procedures and location of stored specimens. Locates specimens and pulls from various departments as requested. | 2/20/2019 |
| 15993 | LabCorp Greenville, NC Specimen Accessioner HS Diploma Exp: 1-2 years |
Prepares laboratory specimens for designated departments/locations prior to laboratory analysis and testing. Unpacks specimens from branches or ports and routes specimens by type to various staging areas. Prepares all specimens received for testing in designated laboratory departments or locations such as staging of specimens, centrifuge, separate serum, and blood smears. Aliquots sample for departments. Prepares excess specimen samples for storage and resolves and document problem specimens. | 2/20/2019 |
| 15994 | LabCorp Phoenix, AZ QA Analyst BS/BA in medical technology Exp: 1-2 years |
Provides leadership in the areas of quality assurance, quality control, quality related training, and standardization compliance within the laboratory. This position is also responsible for project management activities as they relate to identified areas within the laboratory requiring standardization to improve the quality and/or efficiency of operations. | 2/20/2019 |
| 15995 | Lake Pharma Hayward, CA Lab Assistant, Process Development AS or BS in biology or related Exp: 0-2 years |
Responsibilities include but are not limited to: Maintain laboratory instruments, follow SOPs for mammalian cell culture and protein/antibody purification, conduct data input, analysis, and interpretation, think critically and creatively to determine appropriate resources for resolution of problems, recognize and trouble shoot anomalous and inconsistent experimental results. | 2/20/2019 |
| 15996 | AI Therapeutics Guilford, CT Post-Baccalaureate Researcher BS in life sciences Exp: 1+ years |
We are looking for a talented post-baccalaureate researcher with applied experience in molecular and cell biology. Work alongside other experimental biologists, deep learning scientists, computational biologists and a world-class leadership team to help progress a new platform for precision medicine applications. Responsibilities include: Maintain cell lines and primary cultures. Perform in vitro cellular assays to support drug development efforts. Perform biochemical assays to support mechanism of action studies. Perform NGS assays to assay expression signatures and mutations in cell lines and primary tumors. | 2/20/2019 |
| 15997 | Lampire Everette, PA Molecular Biologist BS/BA in biology or related Exp: 1-3 years |
Seeking a highly motivated Research Associate I/II with a background in Molecular Biology to assist in the development of new technologies including CRISPR genome engineering and recombinant antibody generation. The successful candidate will be responsible for learning, researching and implementing recombinant DNA approaches to support research team needs, as well as designing work-flows, and assay development. | 2/20/2019 |
| 15998 | Latitude San Diego, CA Research Associate BS in chemistry, pharmaceutical sciences, or related Exp: 1-5 years |
A successful candidate will possess proficiency in a variety of analytical chemistry techniques including HPLC. The position of Research Associate will report to a Formulation Scientist. Responsibilities include: assist the supervising Formulation Scientist to complete individual formulation development projects, assist in the design, execution and interpretation of formulation development based on the defined deliverables, as well as in the planning of activities to meet the project timelines, and prepare presentations of data and progress and assist in regular presentations to external clients during formulation development projects | 2/20/2019 |
| 15999 | LifeMine Cambridge, MA Research Associate/Senior Research Associate, Synthetic Biology BS in biology, or chemistry Exp: 1-2 years |
We are seeking a Research Assistant with expertise in the use of molecular biology tools such as RNA/DNA extraction, PCR/qPCR, RT-qPCR, plasmid miniprep, and DNA restriction and electrophoresis. Experience in molecular cloning (traditional and seamless aka Gibson), designing constructs, analyzing sequencing data etc. Role will likely evolve to support our effort to engineer and manipulate fungal secondary metabolite clusters to increase the titers of natural product production and establish LifeMine’s fungal genomically-enabled drug discovery platform. | 2/20/2019 |
| 16000 | LifeSensors Malvern, PA Entry Level Scientist BS or MS in biology or related Exp: 0-2 years |
We are seeking individuals who arepassionate about research, bringout of the box thinking and take bold steps todevelopinnovativetechnologies with applications in the ubiquitin research field.Successful candidates will have basic knowledge of biochemistry and molecular biology techniques, in particular experience with, protein expression andpurification and cloning. Knowledge of the ubiquitin proteasome pathwayis desired. | 2/20/2019 |
| 16001 | Lonza Hayward, CA QC Analyst I BS/BA in chemistry or biological sciences Exp: 0-2 years |
This position is responsible for performing biological, chemical and physical analyses on pharmaceutical products through all stages of the manufacturing process from incoming raw materials, in-process, stability and final products. Perform biological, chemical assays for raw materials, initial, in-process, stability and final products.Use sophisticated laboratory instrumentation and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles. | 2/20/2019 |
| 16002 | Lubrizol Corporation Gastonia, NC Chemical Operator HS Diploma Exp: 0 years |
Filtering finished latex from reactors to storage, including: the verification that latex is within all specifications, calculation of correct storage tank capacity, proper sampling and record keeping (valve placement sheets, shift log, filing charts, etc.). Manufacture, packaging and shipment of customer bulk orders, including: the calculation of correct tanker outage/inage, inspection of tanker, proper sampling, completion of weight ticket and bill of lading. Manufacture, packaging and shipment of customer drum orders, including: proper sampling and labeling, completion of packing list and bill of lading and the proper use of forklift. | 2/20/2019 |
| 16003 | Lubrizol Corporation Deer Park, TX QA Lab Technician BS/BA Exp: 0-3 years |
We currently have a challenging and rewarding position for a Lab Technician at our Deer Park, Texas facility. Responsibilities include: Performs test on all in coming raw materials prior to their use in the process, maintains all lab related data systems, including computer and hardcopy formats. Responsible for data systems, including computer and hardcopy formats, and performs regularly scheduled and unanticipated analytical testing on all in-process product and communicates the results to production units. | 2/20/2019 |
| 16004 | Lucigen Middleton, WI International Sales Coordinator BS/BA in business or marketing Exp: 1-2 years |
The International Sales Coordinator provides administrative and management support to LGC, Biosearch Technologies' distribution network, both domestic and international, as well as support to international customers. This position requires excellent customer interaction with both internal and external customers. Responsibilities include: Respond to distributors' inquiries regarding pricing, marketing tools, re-direct technical questions, or special projects such as logistics planning & preparations for distributor meetings, Capture marketing and sales announcements, or corporate updates to develop monthly newsletter for distributors and distribute the newsletter in electronic format to entire distribution network, etc. | 2/20/2019 |
| 16005 | Kantar Warren, NJ Graduate Development Program BS/BA, 3.0 GPA or higher Exp: 0 years |
This is a graduate development program that will provide skill training in areas such as data, client management, leadership, business acumen, and project management over a two-year program. | 2/19/2019 |
| 16006 | Kantar West Chester, PA Custom Product Development Specialist I BS/BA in math, computer sciences, information systems, or realted Exp: 1-3 years |
We are looking for a Jr.-level applications developer to design, build, modify, deploy, and support custom applications to complement existing syndicated applications per our client’s needs. | 2/19/2019 |
| 16007 | Kantar New York, NY Associate, Program Leadership BS/BA in marketing, psychology, or economics Exp: 1+ years market research is plus |
As a member of the Program Leadership team, you will be responsible for executing research projects for existing publisher, agency and advertiser clients. In this role, you will be responsible for project excellence from the point of project sale through final data delivery; acting as the point person between all operational and sales teams to ensure efficient and successful project execution for our clients. | 2/19/2019 |
| 16008 | Kashiv BioSciences Bridgewater, NJ Scientist I - AR&D MS in analytical chemistry, biochemistry, or related Exp: 0-2 years |
A Scientist will be a key technical resource responsible for independently developing methods, generating reliable and interpreting data, using analytical instrument that include HPLC, UPLC, GC, UV/Vis, Mass spectrometer, dissolution apparatus and particle analyzer. This position is also responsible for designing experiments, writing method validation protocols, conducting method validation, and processing and interpreting the analytical data. | 2/19/2019 |
| 16009 | Kashiv BioSciences Bridgewater, NJ Facilities Engineer BS/BA or MS in engineering Exp: 1-3 years |
The Facility Engineer will ensure that all safety standards are followed. Maintenance and inspections will be done to guarantee those cGMP standards are being followed. Performs routine inspections of the equipment. Monitoring of the BMS system and coordinating the PM schedule and maintenance activity. Generate engineering documents for equipment, Facility and utilities and execute the same, Support Project Execution and Vendor Development. Maintain and coordinate to have the updated floor plans and P&ID of the equipment’s and facility. | 2/19/2019 |
| 16010 | KBI Biopharma Durham, NC Research Associate BS/BA or MS in chemistry, biochemistry, or related Exp: 0+ years |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Understands experiments and conducts troubleshooting analysis. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. | 2/19/2019 |
| 16011 | KBI Biopharma Boulder, CO Research Associate BS/BA in chemistry, biochemistry, or related Exp: 0-3 years |
Temporary position. Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Conducts laboratory experiments in support of biopharmaceutical development and process development including running electrophoresis gels, HPLC’s, etc. and preparing buffers. Maintains and updates knowledge and instrumentation and maintenance. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. | 2/19/2019 |
| 16012 | KCAS Shawnee, KS Analyst I BS/bA in sciences Exp: 0-2 years |
The Analyst I is responsible for preparation of reagents and solutions, as well as sample processing under required regulatory documentation. May also analyze data, interpret results or contribute to troubleshooting activities. Conducts sample inventory and carries out lab support duties as assigned, such as inventory of chemicals, washing glassware, waste disposal and/or general cleanup. | 2/19/2019 |
| 16013 | KCAS Shawnee, KS Quality Specialist II HS Diploma Exp: 1+ QA experience |
The Quality Specialist II performs activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements, including document review, audits, inspections, and consulting on quality and compliance issues. Provide training assistance in routine quality and compliance topics. Provides consultation on quality and compliance topics in areas of expertise and assists with quality improvement initiatives as needed. | 2/19/2019 |
| 16014 | Kinovate Life Sciences Oceanside, CA Production Specalist (Chemist) BS/BA in chemsitry or relavent Exp: 1-2 years |
The incumbent in this position is responsible for all production activities at KLS. Directly reporting to the Production Manager and working with the QA/QC analysts, this position will also ensure all production process are documented and executed accurately according to established SOPs. The ideal candidate is a chemist with at a minimum of one year of experience in production of chemical compounds, preferably in a GMP environment. | 2/19/2019 |
| 16015 | KSQ Therapeutics Cambridge, MA Associate Scientist/Scientist, Biotherapeutics Drug Discovery BS or MS in biology or related Exp: 1-5 years |
The successful applicant will work with internal functional groups to help design and execute screening strategies for therapeutic antibody discovery campaigns – including biochemical, molecular, and/or cellular assays for the testing of biotherapeutics from discovery to lead-optimization. Work with internal functional groups to develop, optimize and execute high throughput binding assays (ELISA, Octet, FACS) and cell-based assays (functional, phenotypic, reporter etc.) for screening panels of therapeutic antibody candidates | 2/19/2019 |
| 16016 | KSQ Therapeutics Cambridge, MA Associate Scientist/Scientist, Autoimmunity BS Exp: 0-3 years |
Responsibilities as an associate scientist include querying novel pathways/mechanisms for therapuetic intervention with CRISPR technologies, work as part of an interdisciplinary team to contribute to the design and execution of experiments that support our research activities and project goals, and design, plan, and execute high-quality and well-controlled immunological assays to provide insight into potency and mechanism-of-action . | 2/19/2019 |
| 16017 | Thermo Fisher Scientific Florence, SC Scientist I - R&D BS/BA in chemistry or sciences Exp: 0-2 years |
This is an exceptional entry-level opportunity to assist with the R&D efforts at the Florence, SC facility by conducting important experiments that support our customers with pharma development. Duties include: Conduct chemical experiments and/or analysis in laboratory as instructed by a senior staff supervisor, Accurately record and report experiments and scientific findings per assigned departmental standards in a timely manner to meet project objectives, Maintain a clean and safe work environment within the framework of OSHA, cGMP, safety regulations and Thermo Fisher SOPs | 2/16/2019 |
| 16018 | Thermo Fisher Scientific Mississauga, Ca Complicance Associate (Contract) BS/BA in sciences Exp: 1-2 years |
In this one-year contract position you will support and ensure adherence to established Standard Operating Procedures (SOPs) for conducting and generating the Annual Product Review report. You will act as a liaison between several internal departments with the intent to gather relevant data. Additionally, you will support the compilation of product data for the review period with the objective of verifying the consistency of existing process, the appropriateness of current specifications, highlighting any trends and identifying both product and process improvements for the drug product. Performs administrative tasks of data entry, generates trending reports and statistical data analysis for Annual Product Reports. | 2/16/2019 |
| 16019 | Thermo Fisher Scientific Eugene, OR Scientist, Production (entry level) BS/BA in biology, chemistry, or related Exp: 0-2 years |
As a Scientist I you will work in a manufacturing environment and be responsible for performing protein and dye conjugations while following quality and safety standards. You will follow written procedures, and be technically capable of performing production processes. Responsibilities include: produce/analyze protein products, maintain inventory in lab, analyze and present data. | 2/16/2019 |
| 16020 | Thermo Fisher Scientific Pittsburg, PA Pricing Coordinator I AS degree in business Exp: 0+ years |
Coordinates and administers accurate pricing on ~2000 customer contracts with sales of over $200 Million using Thermo Fisher’s complex pricing systems. Key responsibilities include: Nice price agreement, pricing maintenance, troubleshooting, customer service, and supplier rebates. | 2/16/2019 |
| 16021 | Invivoscribe San Diego, Ca Manufacturing Associate II BS/BA in scientific discipline Exp: 1+ years |
The Manufacturing Associate II contributes to the drafting and reviewing of new documents, including Standard Operating Procedures, Batch Records, Validations, work instructions and Purchasing Specifications. Assists with all aspects of manufacturing, including the production of master mixes, controls and assay kits. Manufactures products adhering to Quality System Regulations and are accompanied by appropriate documentation. | 2/16/2019 |
| 16022 | IQVIA Durham , NC Laboratory Associate 1 BS/BA in scientific discipline Exp: 0-2 years |
Perform routine analysis and laboratory testing procedures to obtain data from client specimens. Provide routine documentation and review of work performed in a timely manner. Responsibilities include: Complete and prepare documentation in compliance with regulatory and corporate guidelines. Perform and document all specimen test procedures with accuracy, consistency and timeliness in accordance with current standard operating procedures (SOPs) and regulatory guidelines. Exercise good judgment in assessing whether test procedure is proceeding according to expectations and that the results are within acceptable tolerances. | 2/16/2019 |
| 16023 | IQVIA Marietta , GA Entry Level Clinical Trial Project Coordinator BS/BA in management, life science or related Exp: 0-2 years |
The Project Coordinator provides support to the Project Manager and related team members by performing generic procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. startup, maintenance and close-out); Ensure work is conducted in line with standard operating procedures, policies and good practices. Using monitoring tools, pro-actively identify trends and provide feedback to internal departments and/or client on performance of both the Investigator and the Q2 Solutions services to ensure timely service delivery. Examples may include: | 2/16/2019 |
| 16024 | IQVIA Durham , NC Lab Associate - Nucleic Acid Isolations and Initial QC BS/BA in scientific discipline Exp: 0-2 years |
Perform routine analysis and laboratory testing procedures to obtain data from client specimens. Provide routine documentation and review of work performed in a timely manner. Perform and document all specimen test procedures with accuracy, consistency and timeliness in accordance with current standard operating procedures (SOPs) and regulatory guidelines. Identify abnormal progress of test procedure, potential QC failures, or otherwise unusual results and escalate to senior lab personnel immediately. | 2/16/2019 |
| 16025 | IQVIA Durham , NC Statistical Programmer - Entry Level BS/BA or MS in mathmatics, biostatistics, or public health Exp: 0-1 years |
Statistical Programming projects vary, your typical responsibilities and opportunities might include: Programming all aspects of a clinical trial, from files to tables, listings and figures Using SAS in a quality control and production capacity Programming from scratch as well as updating existing programs Developing specifications for analysis files and annotating output shells for programming instruction and documentation Working and communicating effectively in a team environmentStatistical Programming projects vary, your typical responsibilities and opportunities might include: Programming all aspects of a clinical trial, from files to tables, listings and figures Using SAS in a quality control and production capacity Programming from scratch as well as updating existing programs Developing specifications for analysis files and annotating output shells for programming instruction and documentation Working and communicating effectively in a team environment | 2/16/2019 |
| 16026 | IQVIA Durham , NC Biostatistician - Entry Level MS in math, statistics, public health Exp: 0-1 years |
Biostatisticians projects vary, your typical responsibilities and opportunities might include: Develop analysis plans, table shells, programming and table specifications; produce tables, listings and figures; perform data review and statistical analysis. Programming aspects of a clinical trial, from files to tables and listings. Assist with protocol development and protocol and case report form (CRF) review. Advise data management staff on database design and critical data. May advise on validation checks. Assist in writing statistical sections of integrated reports. Assist project lead in fulfilling project responsibilities. | 2/16/2019 |
| 16027 | Irvine Scientific Santa Ana, CA Quality Control Microbiologist Level II BS/BA in microbiology Exp: 1-2 years |
We are seeking an individual to perform applicable testing on raw, in-process, and final products to insure material quality as well as to perform tests for monitoring environmental conditions and water quality. Responsibilities include: testing raw, in-process and finished products. Testing environmental conditions, testing water systems, calibrating and maintaining instrumentation, etc. | 2/16/2019 |
| 16028 | McNeil Consumer Healthcare Guelph, Ca Assistant Scientist, Analytical testing- 12 month contract BS/BA in biochemistry, chemistry, biology, or related Exp: 1+ years lab experience |
Under limited supervision and in accordance with all applicable federal, provincial, and local laws/regulations, the Companies’ policies, procedures and guidelines, you will be responsible for: Performing assigned scientific experiments and routine tasks according to established procedures. Coordinating and/or executing: method validations and/or transfers; chemical and physical testing of stability samples; sampling and testing of process validation batches. Assisting in laboratory investigations. Reviewing data and documents. Collating, analyzing, and processing data. Keeping accurate records and supporting the development of technical documentation. | 2/16/2019 |
| 16029 | Jounce Therapeutics Cambridge, MA Research Associate/Associate Scientist BS or MS in biological sciences Exp: 0-2 years |
We are looking for a creative and highly motivated research associate/associate scientist to join the Translational Genomics department at Jounce Therapeutics. The successful candidate will be an integral team member supporting the translational science efforts that help transition novel immune-oncology biologics from bench to bedside. Primary responsibilities include the design and execution of gene expression and genomics-based experiments. In addition, the candidate will work with other lab members to harness and implement new technology within the genomics space. Job responsibilities include careful design and execution of experiments, data analysis and interpretation, thorough documentation of work, and clear communication of results both in group settings and in written reports. | 2/16/2019 |
| 16030 | Jubilant Life Sciences Spokane, WA Associate, Regulatory Affairs BS/BA Exp: 1-2 years |
TheRegulatory Affairs & Pharmacovigilance Associatesupports the regulatory compliance and pharmacovigilance programs by coordinating the scheduled activities of state and federal reporting, as well as medical complaint handling, ensuring compliance with US and International regulatory agencies. This individual evaluates both the compliance and medical complaint report information in order to plan appropriately, request information, and maintain schedule adherence. Responsibilities also include eSubmissions and the assurance that assigned departmental procedures are developed and maintained in accordance with US and/or global regulatory requirements as well as enhancing regulatory compliance systems and strategies. | 2/16/2019 |
| 16031 | Catalent Madison, WI Associate, Quality Assurance Validation BS/BA in technical discipline Exp: 0-2 years |
The Quality Assurance Validation, Associate supports ongoing validation efforts and quality systems responsibilities in support of the manufacturing, testing, and release of formulated drug substance. This role contributes to the development of concepts and techniques specific to validation and risk management. The Quality Assurance Validation, Associate serves as the quality contact for quality projects and continuous improvement efforts regarding Validation and Quality Risk Management. | 2/16/2019 |
| 16032 | Catalent Madison, WI Associate Scientist, Analytical Development MS in chemistry/biochemistry Exp: 1+ years |
The Associate Scientist, Analytical Development is responsible for developing new analytical methods independently and transferring the methods internally or from/to clients. Duties include: Executes all activities related to the analysis of proteins from mammalian cell culture ranging from SDS-PAGE analysis, ELISA analysis, various HPLC based methods, cIEF and product binding assays. The position requires strong documentation skills and the ability to follow SOPs. Independently develops/optimizes analytical methods to characterize protein/antibody, including, but not limited, to RP-HPLC, SEC, cIEF, and CE | 2/16/2019 |
| 16033 | Catalent Madison, WI Associate Quality Assurance Systems, Document Control BS/BA in biology, biotech, or engineering Exp: 0-2 years |
The Associate Quality Assurance Systems, Document Control is responsible for managing the flow of document review, making documents effective and distribution according to standard operating procedure (SOP). The Associate Quality Assurance Systems, Document Control will correspond with customers to obtain document approval. Responsible for the process of document control, including managing drafts, editing, approval, change control, distribution and archiving, of all controlled documents (e.g. Standard Operating Procedures (SOPs), Batch Production Records, Stability Protocols, Qualification Protocols, Specifications, Equipment Records, etc). Edits Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and reports independently and accurately. | 2/16/2019 |
| 16034 | Catalent Strathroy , Ca Documentation Associate HS Diploma or GED Exp: 1-3 years in documentation |
The Documentation Associate will support the creation, review, and processing of general documents and batch records. The Documentation Associate is also responsible for issuing, distributing, and reviewing documents in a timely and efficient manner. Responsibilities include: Creating and updating master documents, issuing a copy of the current approved master documents for packaging or manufacturing; Compiling, summarizing and reporting information from the batch records as required; Accurately controlling the electronic and paper versions of all documents such as Standard Operating Procedures, Master Forms, Packaging Instructions and Production Batch Records; | 2/16/2019 |
| 16035 | Celegene San Diego , CA Catalent MS in Organic chemistry Exp: 1-5 years |
This position is responsible for activities associated with the development of small molecule active pharmaceutical ingredient (API) within Celgene and in contract development and manufacturing organization (CDMO). The individual would be expected to investigate and execute syntheses of complex molecule, develop scalable chemical manufacturing processes, and assist with technology transfers to CDMOs. He/ She will also serve as a resource of scientific and technical expertise and assume some departmental responsibilities for assigned projects and equipment. | 2/16/2019 |
| 16036 | Celegene Warren, NJ Associate Scientist, CAR T Product Sciences MS in biology, immunology, or biomedical engineering Exp: 1-3 years |
As part of the Product Sciences group, the energetic and motivated scientist will design, perform and interpret complex experiments related to the development of novel analytical tools and characterization of the final product and process intermediates for CAR-T products. This role will support the activities related to the identification of product critical quality attributes, in collaboration with Process/Analytical Development, Translational Development, Clinical and Immuno-Oncology research functions. | 2/16/2019 |
| 16037 | Just Biotherapeutics Seattle , WA Associate Scientist, Analytical BS Exp: 0-3 years |
Just is seeking a motivated and creative scientist who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work with a multidisciplinary team for the analytical and functional testing of large molecule therapeutics and analysis of process impurities. The successful candidate will have some experience with DNA purification, PCR and ELISA assays. The candidate should possess strong written and verbal communication skills, strong organizational skills, a desire to learn new scientific concepts, the ability to multitask and an ability to work directly with scientific staff across multiple disciplines. | 2/16/2019 |
| 16038 | Just Biotherapeutics Seattle , WA Associate Scientist, Functional Biocharacterization BS Exp: 0-5 years |
Just is seeking a motivated and creative scientist who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work with a multidisciplinary team for the analytical and functional biocharacterization of large molecule therapeutics and analysis of process impurities. Experience with HPLC and CE methods, DNA extraction, PCR and ELISA binding assays preferred. Cell-based and ligand-receptor binding assays, as well as high-throughput methods and liquid handling robotics beneficial. The successful candidate has strong written and verbal communication skills and is interested in ways to improve technology. The ability to multitask and to work both independently and in teams in a fast-paced collaborative environment is necessary. | 2/16/2019 |
| 16039 | Just Biotherapeutics Seattle , WA Process Engineer I, Purification BS Exp: 0-3 years |
Just is seeking a highly motivated entry-level manufacturing Process Engineer(s) that desires a significant opportunity to improve worldwide access to biotherapeutics. This team member will be responsible for the manufacture of mammalian cell-based biotherapeutics for clinical use under cGMP conditions. Under direct/moderate supervision, job responsibilities include set-up, operation, and maintenance of disposable-based manufacturing equipment; execution of manufacturing process operations; and assist in general lab operations. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures, and manufacturing documentation. | 2/16/2019 |
| 16040 | Immunomedics Morris Plains, NJ Cell Culture Technologist, Upstream Process & Manufacturing BS/BA in biology or related Exp: 1-3 years |
The Cell Culture Technologist, Upstream Process and Manufacturing Sciences is responsible for participating in the operation of mammalian cell culture processes under cGLP conditions. Responsibilities include: Prepares and maintain cGLP research cell banks. Performs cell culture expansion under cGLP for cell culture in benchtop bioreactors and shake-flasks.Strong aseptic techniques and demonstrated ability in documentation and knowledge of cGMP/cGLP cell culture development. | 2/14/2019 |
| 16041 | Immunomedics Morris Plains, NJ QC Analyst, Raw Materials BS/BA in biology, chemistry, or related Exp: 1-3 years |
The QC Analyst, Raw Materials is responsible for release testing of incoming raw materials and utilities (water and gas) samples testing. The incumbent will be supporting testing and method validation activities either inhouse or at a third-party provider. The responsibilities may also include receiving, inspection and sampling of incoming raw materials as assigned. This position also includes responsibility for authoring technical reports, specifications for incoming raw materials and evaluation of change notifications, as directed. | 2/14/2019 |
| 16042 | Impel Seattle , WA Pharmaceutical Formulation Technician BS/BA in chemistry, pharmaceutical sciences or related Exp: 0-5 years |
The Pharmaceutical Formulation Technician will conduct formulation and process development for powder and liquid nasal dosage forms under the supervision of the Pharmaceutical Formulation Scientist. Responsibilities include: Conduct laboratory experiments under the supervision of the formulation scientist. Assist technical staff in the development of Impel’s drug formulations. | 2/14/2019 |
| 16043 | In Cube Labs San Jose, CA Mechanical Engineer I BS/BA in mecahnical engineering or related Exp: 1+ years |
The ideal candidate is expected to play a pivotal role in our R & D team. The candidate must have a background in mechanical engineering. Experience with design, fabricating and assembling medical products is highly desired. Responsibilities include: creating/updating/releasing engineering designs, designing tools for manufacturing, working with outside vendors, develop test protocols and reports. | 2/14/2019 |
| 16044 | Inova Diagnostics San Diego, CA Chemist I - Bioflash Manufacturing BS/BA in biological sciences Exp: 1-2 years lab exerience |
Participates in the preparation of autoimmune diagnostic products, utilizing the Bioflash technology platform, following established procedures. Major duties include Bioflash bead and reagent preparation activities and the preparation of controls and conjugates for the Bioflash product lines. | 2/14/2019 |
| 16045 | Inova Diagnostics San Diego, CA Chemist I- Research & Development BS/BA in biological sciences Exp: 1-2 years lab exerience |
Assists with the development of new or improved autoimmune diagnostic assays according to established procedures. Major research and development duties include assistance with reagent formulation and optimization of existing formulations. Additional duties involving organizing and facilitating timely progress and completion of projects will be assigned. | 2/14/2019 |
| 16046 | Inovio Pharmaceuticals San Diego, CA Laboratory Assistant (Logistical Operations) AS degree in biological sciences Exp: 0-1 years |
The Laboratory Assistant provides assistance with lab management functions to support all aspects of research within the company. The position interfaces with multiple departments (R&D, engineering, accounting, quality) and performs general lab maintenance duties and recordkeeping. | 2/14/2019 |
| 16047 | Inovio Pharmaceuticals Plymouth Meeting, PA Clinical Trials Associate BS/BA Exp: 0-2 years |
The Assistant, Clinical Trials (CTA) is responsible for supporting, under the direct supervision of the supervisor/Clinical Project Lead (CPL), clinical trial execution, externally sponsored research and program level activities as assigned within Clinical Operations at Inovio. This position assists in various tasks and projects related to clinical trials as well as basic, administrative duties such as ordering drugs and devices, maintaining milestone trackers and filing of essential documents of externally sponsored trials. | 2/14/2019 |
| 16048 | Insmed Bridgewater, NJ Complaint Associate, Quality Asurance BS in engineering or life sciences Exp: 1-2 years |
Reporting to the Associate Director, Quality Assurance - GMP, the QA Complaint Associate, will play a key role in the complaint process and related customer interactions. This role has a critical interface with the commercial Patient Support Program and will work directly with the team on a daily basis to manage product complaints, device inquiries and support. Specific areas of responsibility include: Complaint intake/entry into Veeva, ensuring accurate and thorough complaint intake information, Preliminary assessment of all complaints within 24 hours for regulatory escalation and replacement need, trouble-shooting with complainant, maintaining work instructions, patient follow-ups as needed, etc. | 2/14/2019 |
| 16049 | Omnipod Acton, MA Regulatory Affairs Assocaite - LAF BS preferred Exp: 0-2 years |
The position of Regulatory Affairs Associate will be responsible to provide immediate administrative regulatory support to ensure timely introduction of advertising and promotion content in the U.S, as well as opportunity in the future to support new products subject to medical device regulations in both the U.S. and global regions. Provide regulatory support to marketed products and ensure company’s regulatory compliance status. Responsibilities include: Manage regulatory databases and administer regulatory processes, primarily advertising and promotional content, which includes activities such as data management and verification, Support the development and implementation of regulatory processes, procedures, and standards as assigned. | 2/14/2019 |
| 16050 | Omnipod Los Angeles, CA Clinical Services Specialist - West BS/BA Exp: 0-2 years |
The Clinical Services Specialist (CSS) is primarily responsible for meeting required sales quota and all clinical initiative expectations. This responsibility will require extensive travel and extended stays in a field based territory to support open territory needs. The CSS will provide product sales, training, downloading and technical support in accordance with company policy. They will also in-service physicians, mid-level staff, CDE’s, and ancillary staff on the OmniPod Insulin Management System, build relationships with our customers, and bec skilled at selling and using the OmniPod Insulin Management System. | 2/14/2019 |
| 16051 | Integer Chaska, MN Supplier Quality Engineer I BS/BA in related field Exp: 0-2 years |
The primary purpose of this position is to develop the risk-based supplier management process, lead the critical supplier-related projects, and support daily supplier non-conformances and requests for change. This position will also be responsible for performing GMP/ISO audits on suppliers, proposing improvements to their quality system and tracking the closure of any audit related non-conformance. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. The primary purpose of this position is to develop the risk-based supplier management process, lead the critical supplier-related projects, and support daily supplier non-conformances and requests for change. This position will also be responsible for performing GMP/ISO audits on suppliers, proposing improvements to their quality system and tracking the closure of any audit related non-conformance. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. The primary purpose of this position is to develop the risk-based supplier management process, lead the critical supplier-related projects, and support daily supplier non-conformances and requests for change. This position will also be responsible for performing GMP/ISO audits on suppliers, proposing improvements to their quality system and tracking the closure of any audit related non-conformance. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. | 2/14/2019 |
| 16052 | Integer Plymouth, MN Associate Prototype Technician - 2 AS degree or above Exp: 0-3 years |
The primary purpose of this role is to perform assembly and inspection operations over a range of new products and/or processes. Will support non-cyclical work which may include prototypes and pre-production lots in preparation for validation, clinical trials or transfers. Will also support multiple builds within the facility including lab and cleanroom environments. With guidance from Engineering on projects and using work procedures, this role provides support to the Engineering teams to meet various deadlines. May provide support to other team members or provide input to the Engineers on assembly, processes, and build/quality documentation. | 2/14/2019 |
| 16053 | Integra Plainsboro, NJ Quality Control Analyst I BS/BA in biological or chemical sciences Exp: 0-3 years |
The Quality Control Analyst I will be responsible for executing laboratory testing and data analysis, as well as, assist with test methods development, validation development and implementation. Tests and inspects raw materials, work-in-process (WIP), and finished goods at various stages of production process. Selects random samples for tests at specified stages such as incoming or in production process, and tests products for variety of qualities, such as dimensions, performance, appearance, correct assembly, and other testing outputs. Records test data, applying statistical quality control procedures. Works collaboratively with Manufacturing, Engineering, Quality Assurance, and other functional experts to support all daily operational activities. Consults with management to resolve quality, production, and efficiency problems. Functions in conjunction with manager and functional experts on special department projects. Works with internal departments to ensure implementation, maintenance, and improvement of the quality management system. Performs the essential duties and responsibilities as listed in section below. | 2/14/2019 |
| 16054 | Integra Plainsboro, NJ Microbiologist I HS Diploma, BS/BA in biology preferred Exp: 0-3 years |
As a Microbiologist I, duties include: Ensure compliance with all company policies and procedures and appropriate regulations, including FDA and ISO 9001, ISO 13485, CMDR and the Medical Device Directive. Perform and document in-house microbiological testing on all in-process and finished products to comply with acceptance requirements. Perform LAL, water analysis, growth promotion, gram staining, identification of microorganisms and other microbiological testing. Perform and document environmental monitoring in compliance with Standard Operating Procedures. Report any equipment and testing deviations to the Supervisor. Submit samples for shipment to third party labs when necessary. Maintain GMP/GLP laboratory notebooks and documentation relevant to the duties and responsibilities assigned. | 2/14/2019 |
| 16055 | Integral Molecular Philadelphia, PA Research Associate I BS/BA in biology, bioengineering, or related Exp: 1-2 years lab exerience |
As a research associate, responsibilities include: Conduct laboratory research and support general R&D efforts for customer-based biomedical research, projects may involve cell culture, virology, DNA preparation, and liquid-handling automation, prform cell-based assays (Western blot, ELISA, immunofluorescence, flow cytometry) | 2/14/2019 |
| 16056 | IDT Coralville, IA Synthesis Scientist I - Main Production Nights BS/BA in sciences Exp: 0-2 years |
The Synthesis Scientist I synthesizes custom oligonucleotides according to the customer’s order. This generally includes synthesis, cleavage, deprotection and QC sampling of the products being made. Other responsibilities include adherence to lab SOPs, maintaining lab equipment/stock, keeps record of specalized processes for oligo, etc. | 2/14/2019 |
| 16057 | IDT Coralville, IA Custom Quality Control Analyst I - SAG Group BS/BA in biological or chemical sciences Exp: 0-2 years |
The Custom Quality Control Analyst I ensures the quality of processes and products in support of all manufacturing areas within Integrated DNA Technologies. Essential functions include: analyze data for quality/consistency/accuracy, handels samples for preperation fore assays, understands ISO requirements, etc. | 2/14/2019 |
| 16058 | IDT Coralville, IA Manufacturing Chemist BS/BA in biological or chemical sciences Exp: 0-2 years |
The Manufacturing Chemist efficiently produces high quality materials for use in IDT’s production labs. Essential Functions include: monitoring inventory, follows processes for manufacturing/storage/transportation, gathers/interprets/analyzes oligo data, maintains accurate/detailed product/process, intstrument and training. | 2/14/2019 |
| 16059 | Integrity Bio Camarillo, CA Research Associate BS/BA in biochemistry, chemistry, biology, or related Exp: 1-5 years |
Duties and functions include: assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision, set up/perform HPLC as well as other assays to characterize protein/peptide molecules, analyzes data, etc. | 2/14/2019 |
| 16060 | Integrity Bio Camarillo, CA Project Management Associate BS/BA in biochemistry, chemistry, biology, or related Exp: 0-5 years |
Duties and functions include: Schedule and attend meetings, draft agendas, lead discussions, author meeting minutes, and follow up on action items, Assist in designing client studies and generateproposals outlining scope, material requirements, schedule, and budget, Coordinate execution of projects with IBI project teams, put together study timelines, oversee submission of data, and respond to client inquires | 2/14/2019 |
| 16061 | Intuitive Multiple Locations, Field Service Engineer AA degreen in electornics or engineering Exp: 1-3 years |
Install and support the Intuitive Surgical products and ensure service agreements and warranty obligations are fulfilled. Exceed customer expectations and maintain customer satisfaction to the highest possible level. Pre site verifications to prepare site for system installation. Assist in coordination of system delivery (e.g. confirming site readiness). Perform system installations. Install system upgrades. Provide technical and clinical support to end-users and other ISI employees. Train customer on new features or enhancements made to existing features. Install and support the Intuitive Surgical products and ensure service agreements and warranty obligations are fulfilled. Exceed customer expectations and maintain customer satisfaction to the highest possible level. Pre site verifications to prepare site for system installation. Assist in coordination of system delivery (e.g. confirming site readiness). Perform system installations. Install system upgrades. Provide technical and clinical support to end-users and other ISI employees. Train customer on new features or enhancements made to existing features. | 2/14/2019 |
| 16062 | Intuitive Milford, CT Mechanicl Design Engineer - Advanced Energy Insturments BS or MS in mechanical engineering Exp: 0-3 years |
The Mechanical Design Engineer will help develop new Advanced Energy instruments while addressing performance, cost, and reliability requirements and completing the development, documentation, and verification of those designs. The successful candidate will have both the technical depth to resolve complex mechanical, materials and manufacturing design issues and the ability to work in an interdisciplinary team to troubleshoot to root cause higher level system issues. A strong sense of shared responsibility and shared reward is required as well as a commitment to high product quality. | 2/14/2019 |
| 16063 | Invitae San Francisco, CA BS/BA in biological sciences Exp: 1+ years |
As part of the pipeline engineering team, you will be responsible for maintaining, improving, and adding to our catalog of production bioinformatics pipelines across an expanding set of modern assays. | 2/14/2019 |
| 16064 | Hovione East Windsor, NJ Process Technician - Drug Product Continuous Manufacturing BS in engineering, or chemical engineering Exp: 1/2 years or more |
The Process Technician will support the installation and qualification of a GMP continuous tablet manufacturing line, highly automated, with Process Analytical Technology enabled control. This position will also support the development and manufacturing activities for drug product and formulation development projects. Work in a GMP environment area, executing chemical and physical operations following approved written instructions and in accordance with cGMPs and EHS regulations. Clean/verify proper cleaning of equipment and production areas according with cGMPs. Adhere to the necessary gowning requirements and in alignment with the various room classifications. Ensure that performed activities are recorded in applicable documentation. | 2/13/2019 |
| 16065 | Hovione East Windsor, NJ Associate Quality Assurance Specialist BS in engineering, or chemical engineering Exp: 1/2 years or more |
The Quality Assurance Associate Specialist promotes high quality standards and a continuous improvement culture within the Quality area of the New Jersey site in order to ensure that these are aligned with applicable quality regulations and the company's high quality standards. This role provides support in achieving the department objectives and supports the cGMP programs (i.e. validation, qualification, stability, and environmental control). | 2/13/2019 |
| 16066 | Human Longevity San Diego, CA Oncology Bioinformatics Laboratory Scientist BS or MS in computer science, bioinformatics or related Exp: 0-2 years |
The Oncology Bioinformatics Laboratory Scientist will work closely with the Oncology R&D team to provide informatics support across multiple applications of somatic variant calling using next-generation sequencing technologies. An ideal candidate will have experience developing/implementing somatic variant calling analysis tools in a CLIA/CAP NGS laboratory. This role will be required to participate in the design and execution of validation studies to support the key objectives of the Oncology division. | 2/13/2019 |
| 16067 | ICUmedical San Clemente, CA R&D Engineer BS in mechanical or engineering discipline Exp: 0-2 years |
The R&D Engineer is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. The key responsibility of this position is the design, development, and improvement of product lines to ensure their efficiency and reliability. The incumbent will be heavily involved with plastics, polymers, molding, medical disposables, plastics engineering, and solid modeling. The R&D Engineer will be expected to interface with customers and suppliers on high-volume disposable medical device design. | 2/13/2019 |
| 16068 | ICUmedical Salt Lake City, UT Production Planner BS/BA Exp: 0-2 years |
As a production planner you will analyze, plans and prepares production schedules for manufactured products within the production facility to meet customer demand. Draws up production schedules to establish sequence and lead time of each operation to meet shipping dates according to sales forecasts and/or customer orders. Analyzes production specifications and plant capacity data and performs mathematical calculations to help determine manufacturing processes, tools, and human resource requirements. Gathers performance data and assesses whether or not departments are performing according to production schedules. Produces reports that evaluate plant capacity and identify areas where improvements can be implemented. | 2/13/2019 |
| 16069 | Idexx Westbrook, ME Lab Associate - Infectious Disease R&D Lab Operations HS Diploma or AS Exp: 0-2 years |
You will be joining the cross-functional R&D Lab Operations team responsible for building research and development SNAP devices, supporting acquisition of diagnostic samples for R&D product testing, and supporting general laboratory operations. The successful candidate will be a self-starter, motivated and excels in a highly collaborative laboratory environment. | 2/13/2019 |
| 16070 | iFyber Ithaca, NY Micro/MolecularResearch Associate BS/BA in biological sciences Exp: 1+ years research experience |
iFyber is seeking aresearch associateto assist with R&D projects at the interface between chemistry, biology, and material science. iFyber serves clients in the medical device, diagnostics, and antimicrobial industries. The person in this position will support a variety of programs that will require experience and/or the ability to pick up bench skills related to microbiology. Responsibilities include: Conduct microbiologyexperimentsboth independently and in a collaborative fashion, Plan tasks for successful completion of experiments based on requirements set by senior staff, Follow established protocols and work with senior staff to adapt or design new protocols | 2/13/2019 |
| 16071 | Imbed Bio Fitchburg, WI Production Technician BS/BA in sciences Exp: 1-4 years work in lab/production environment |
Work with Medical Device Production team in a moderate-volume commercial laboratory to fabricate polymeric films, perform and assist in daily laboratory tasks and work flow, maintain and edit standard operating procedures and work instructions, record data, write reports and communicate results. Ensure quality control of materials and end products of the company in a consistent manner. | 2/13/2019 |
| 16072 | Illumina Bay Area, CA Systems Engineer 1 BS/BA in eletrical, biomedical, mechanical, or chemical engineering Exp: 1-3 years in product development, experience in programing |
We are seeking a Systems Engineer 1 to help us build the next generation of clinical diagnostic tests. This position work with external and internal partners in Operations, R&D, and Software Development to develop new laboratory automation and diagnostic equipment. This engineer will focus on development and system testing activities for our sample preparation systems. Responsibilities include: Participate in development of consumables, assay automation processes to accomplish development and product goals. Conduct screening and troubleshooting experiments to assess the technical capability and performance of assay, robotic, fluidic, sensor, and instrumentation sub-systems and systems, collaborating with senior engineers and scientists. | 2/13/2019 |
| 16073 | Immatics Houston, TX Laboratory Support Assistant AS degree in biological sciences Exp: 1+ years |
The primary purpose of the Laboratory Support Assistant position is to provide support to the research and manufacturing teams to assist in laboratory maintenance and logistics coordination. In addition, provide support to the clinical team in support of adoptive cellular therapy (ACT) clinical trials. This position will report to the Director QA/QC. The primary purpose of the Laboratory Support Assistant position is to provide support to the research and manufacturing teams to assist in laboratory maintenance and logistics coordination. In addition, provide support to the clinical team in support of adoptive cellular therapy (ACT) clinical trials. This position will report to the Director QA/QC. The primary purpose of the Laboratory Support Assistant position is to provide support to the research and manufacturing teams to assist in laboratory maintenance and logistics coordination. In addition, provide support to the clinical team in support of adoptive cellular therapy (ACT) clinical trials. This position will report to the Director QA/QC. The primary purpose of the Laboratory Support Assistant position is to provide support to the research and manufacturing teams to assist in laboratory maintenance and logistics coordination. In addition, provide support to the clinical team in support of adoptive cellular therapy (ACT) clinical trials. This position will report to the Director QA/QC. | 2/13/2019 |
| 16074 | Immatics Houston, TX Research Associate - CMC BS/BA or MA in biological sciences Exp: 1-3 years |
The primary purpose of the research associate position is to perform complex, highly specialized and time sensitive technical cell manipulation and testing procedures to perform experiments pertaining to process, product, or assay development of cell and gene therapy products. Responsibilities include: Performs aseptic cell growth and manipulation procedures such as cell isolation or enrichment, sorting, culture, cellular product cryopreservation, and cell product thaw/wash. Performs and handles human peripheral blood for processing and product manufacture. Perform cell-based studies or assays for product development, assay development, or product characterization. | 2/13/2019 |
| 16075 | Immucor Norcross, GA Red Blood Cell Processing Technician BS/BA in life sciences Exp: 1-3 years |
As a Red Blood Cell Processing Technician, you will perform production tasks in a clean-room environment. In addition, it will be your responsibility to ensure that your work is consistently in compliance with Good Manufacturing Practices and Good Documentation Practices. Additional duties include: Performing blood processing operations according to corporate policies, operating procedures, specifications, and verbal work instructions. Ensuring that blood products are transported, processed and stored in a manner that prevents contamination.Following appropriate control measures to prevent mixing of dissimilar production components in compliance with Good Manufacturing Practices | 2/13/2019 |
| 16076 | Immunogen Waltham, MA RESEARCH ASSOCIATE I MS in life sciences Exp: 1 year |
Develop and troubleshoot LC/MS assays (pharmacokinetic analysis of free payload and antibody, metabolite profiling, drug-antibody ratio measurement) using TTOF 6600, 5500 Triple Quad, Sciex OptiFlow, and Versette instrumentations to support pre-clinical and clinical studies. Test pre-clinical samples to support candidate identification for early development phases. Analyze and interpret data; communicate results and interpretation. Plan experiments, troubleshoot when needed, summarize results, write and review technical reports. Collaborate with project team leaders to organize timelines for assays needs and sample testing. Summarize and present results in internal meetings. | 2/13/2019 |
| 16077 | Medtronic Irvine, CA Manufacturing Engineer MS in engineering or science Exp: 0-2 years |
We are seeking a hands-on Manufacturing Engineer to work closely with R&D, Operations and Quality in the development of new processes necessary to produce Catheters/Delivery Systems/Stents for a lean manufacturing environment. Manage development builds, develop new manufacturing processes, implement and qualify production equipment and methods, generate testing protocols and reports, and work with minimal direction for NPI. | 2/8/2019 |
| 16078 | Medtronic Boulder, CO FPGA DEVELOPMENT ENGINEER MS in electrical engineering or computer science Exp: 0-2 years |
The FPGA Development Engineer will be a member of the Medtronic R&D team working on development and support of electrosurgery generator products. FPGA Engineers can apply their education and talents in FPGA development for embedded systems, including the understanding of how software interacts with hardware. The position is a hands-on development role with a dynamic set of responsibilities in design and verification of embedded systems including RTL coding, simulation, and laboratory testing. | 2/8/2019 |
| 16079 | Medtronic North Haven, CT Associate Chemist (Quality Dept.) BS/BA Exp: 0 years |
Collaborates with engineering and manufacturing functions to ensure quality standards are in place. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality Performs chemical evaluations of new and existing products and processes. | 2/8/2019 |
| 16080 | GigaGen South San Francisco, CA Research Assistant BS/BA Exp: 1-3 years research experience |
GigaGen seeks a talented, highly motivated Research Assistant to work alongside PhD-level scientists on research. This project involves high-throughput discovery and development of therapeutic antibody drug candidates from human and mouse immune repertoires. The work involves significant cell culture work, including a bioreactor and flow cytometry. | 2/7/2019 |
| 16081 | Gilead Foster City, CA Process Engineer II - Solid Dose Manufacturing MS in science field Exp: 0 years |
As a process engineer you will be responsible for: determining functions most critical to departmental success/supports priorities accordingly, manages processes across functions/teams, manages budget for pharmaceutical/packing engineering-related projects. etc. | 2/7/2019 |
| 16082 | Ginkgo Bioworks Boston , MA Research Associate - NGS BS/MS in biology, bioengineering, biochemistry, or related Exp: 1+ years |
As a research associate you will operate high-throughput semi-automated NGS processes, monitor and report on process and perform analysis, suggest and validate process improvements using knowledge of molecular and microbiology | 2/7/2019 |
| 16083 | Ginkgo Bioworks Boston , MA Research Associate - Protein Engineering BS/MS in biology, bioengineering, biochemistry, or related Exp: 1+ years |
We are looking for someone who is excited about the field of synthetic biology and loves a challenge. Responsibilities include enzyme purification and characterization. We want a person who is eager to learn and has a desire to utilize automation to work more efficiently. Our ideal candidate will elevate our team through creative solutions while working closely with other foundry groups. | 2/7/2019 |
| 16084 | Glaukos San Clement, CA Engineer, Research and Development BS/MS in mechnical engineering, or MBA Exp: 0-2 years |
The Engineer, I will perform a variety of mechanical engineering activities on the ocular related products including product design, concept prototyping, concept testing, and early development, clinical builds, manufacturing scale up development and sustaining activities. Responsibilities include developing creative solutions to design and manufacturing problems, ensuring the proper engineering deliverables are accurately generated, generation of 3D CAD models, 2D CAD drawings, test procedures, etc, project management/ leadership, maintaining schedule and product release plans. This individual will may lead project teams with other engineers, designers, and manufacturing staff with a focus on meeting product specifications with technically strong, high quality, cost effective designs following Glaukos’s defined development process. Further, all duties shall be performed in a professional way with attention to detail while supporting Glaukos’ Quality Policy and the appropriated regulatory agencies, including FDA Quality System Regulations (21 CFR 820), ISO Standards (EN ISO 13485) and Risk Management (EN ISO 14971). | 2/7/2019 |
| 16085 | GSK Rockville, MD Associate Biochemist BA/BS in chemistry, biochemistry, molecular biology, or related Exp: 0-2 years |
Responsibilities as an associate biochemist include: coordinating routine in-process biopharmaceutical materials, bulk bio-pharmaceutical ingredients, finish bio-pharmaceutical products/stability sample testing. Conduct/document routine compendial, chemistry, immunology and molecular biology analytical testing for in-process, release and stability samples per SOP. Operate/aintain QC lab equipment. | 2/7/2019 |
| 16086 | GSK Rockville, MD Biopharmaceutical Manufacturing Associate II BS/BA in related field Exp: 0 years |
A Bio-pharmaceutical manufacturing Associate II performs all production operations in the area of assignment within the Rockville Manufacturing facilities. Support Start-up/changeovers/tech transfer activities and perform production operations in areas assigned. Duties include: preparation of buffers and medias and other solutions, following written procedures and batch records. Operate process equipment such as tanks, CIP/SIP skids, agitators, filtration devices, integrity testing and other small equipment following a high standard of GMP compliance and SOP and BRs as written. | 2/7/2019 |
| 16087 | GSK Upper Providenc, PA Associate Scientist / Scientist, Biopharmaceutical Product Sciences BS or MS in pharmacuetics, biology, chemistry, or related Exp: 1+ years lab experience |
The successful candidate will join a Product Development Team within the Biopharmaceutical Product Sciences (BPS) department of the Biopharm Product Development & Supply organization within GSK R&D. The candidate will focus on developing protein formulations, assessing product stability, implementing biopharmaceutical drug product manufacturing processes, and when applicable, coordinating with Device Engineering for implementation of drug delivery devices. The scientist in this role may be expected to contribute to cross-functional initiatives and/or rotate between other BPDS departments to support a flexible product development initiative. | 2/7/2019 |
| 16088 | GSK King of Prussia, PA Biopharmaceutical Manufacturing Associate II BS/BA in science/engineering Exp: 0-1 years |
Under the direction of senior personnel, performs production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. | 2/7/2019 |
| 16089 | GSK Hamilton, MT Manfacturing Associate BS/BA in related field Exp: 1-2 years |
As Value Stream Manufacturing Associate you will manage/lead/be responsible for performing duties as assigned with respect to quality, timeliness, quantity and cost. Work individually and as a team to deliver cGMP compliant product. Adhere to GSK policies, procedures and support site goals. Complete documentation in line with regulatory, GSK, and departmental requirements. Work and communicate closely with other departments both inside and outside of the Value Stream. | 2/7/2019 |
| 16090 | Global Pharma Tek Edison, NJ Pharmacovigilance Scientist BS/BA in science or engineering Exp: 0-2 years |
Pharmacovigilance Scientist. Jobs located in Edison, NJ. Review non-serious and serious AEs and aggregate AE listings. Prepare signaling meeting presentations in collaboration with the team, including a review of events of interest, initial trending of AEs, set thresholds for escalation, and preparation of meeting minutes. Monitor the safety profile of assigned compounds to identify any safety signals and support execution of plans for signal evaluation. | 2/7/2019 |
| 16091 | Global Pharma Tek Edison, NJ Process/Validation Engineer BS/BA in pharmacy, life sciences or related Exp: 1-2 years |
Reviews standard operating procedures which are related to each equipment according to 21 CFR part 11.Uploads developed protocols in the company’s record website by following the procedures.Prepares riboflavin solution in biological quality lab by following the procedure and uses on vial washer and puck washer to test spray coverage test on filling lines.Prepares biological samples to verify the sterility of the heating and cooling zones in depyrogenation tunnel.Witnesses’ vendor SAT (Site Acceptance Test) protocol and execution of all equipment associated with each filling lines.Calculates particle count at the equipment on the Abboject and Ampoule filling lines to verify if rooms are maintaining Grade A aseptic conditions.Performs smoke studies to verify the laminar flow hoods are working consistently throughout in Grade A aseptic conditions. | 2/7/2019 |
| 16092 | Global Pharma Tek Edison, NJ Drug Safety Associate BS/BA in Pharmaceutical science or related Exp: 1-2 years |
Global PharmaTek, LLC has job openings for Drug Safety Associate.Jobs located in Edison, NJ and various unanticipated locations throughout the U.S.Receives clinical study SAE reports, review for medical/regulatory content and assure accuracy per protocol requirements, obtaining follow up as needed; ensure that all SAE’s are complete prior to database closure Process and distributes clinical study SAE reports as per the company SOPs Completes AE/SAE reconciliation prior to clinical trial database closure Receives, processes, and distributes spontaneous adverse event reports for marketed products, both serious and non-serious, as per the company’s SOP’s .Processes all types of adverse event reports utilizing the ARIS safety database Assists with preparing and/or reviewing safety summaries for Investigator Brochures and annual reports, safety submissions for marketed products, and other safety reports as needed or requested | 2/7/2019 |
| 16093 | Goodwin Biotechnology Plantation, FL Upstream Manufacturing Manager BS in biology or physical sciences Exp: 1-2 years cell culture experience |
ssists in all Upstream Development/Manufacturing activities including; cell culture, cell banking, media optimization, seed train design, feed strategy, bioreactor parameter optimization, harvest clarification, and technology transfer to manufacturing. Responsible for the execution of a Manufacturing Batch Records (MBR) for specific projects to manufacture cell derived biopharmaceuticals in compliance with cGMP guidelines and regulations. Activities include cell culture in various cell culture vessels including preparation of inocula for bioreactor production, and operation of various bioreactors. Department responsibilities also include cell culture process development activities, consisting of cell line characterization, media formulation evaluation, and inoculum process development. ssists in all Upstream Development/Manufacturing activities including; cell culture, cell banking, media optimization, seed train design, feed strategy, bioreactor parameter optimization, harvest clarification, and technology transfer to manufacturing. Responsible for the execution of a Manufacturing Batch Records (MBR) for specific projects to manufacture cell derived biopharmaceuticals in compliance with cGMP guidelines and regulations. Activities include cell culture in various cell culture vessels including preparation of inocula for bioreactor production, and operation of various bioreactors. Department responsibilities also include cell culture process development activities, consisting of cell line characterization, media formulation evaluation, and inoculum process development. | 2/7/2019 |
| 16094 | Gore Flagstaff, AZ Industrial Engineer BS in supply chain, industrial engineering, or related Exp: 1+ years lab experience |
As an industiral engineer you will be responsible for: leading cross functional operation projects, drive financial analysis, ensure execution of quantitative project management deliverables within projects such as project cost benefit analysis and metrics of project success, etc. | 2/7/2019 |
| 16095 | Grand River Aseptic Manufacturing Grand Rapids, MI Aseptic Manufacturing Associate HS Diploma, BA/BS preferred Exp: 0-1 years |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. Candidates must be willing to work 2nd or 3rd shift. | 2/7/2019 |
| 16096 | Halo Pharma Whippany, NJ Inspector Quality Assurance HS Diploma Exp: 1-2 years |
The Inspector Quality Assurance (2nd shift) is responsible for performing duties related to but not limited to In-coming materials (i.e. sampling , review specification and release materials in SAP and any other related electronic database), Line Inspections in SDF, Santyl and Packaging lines, review batch records when required, perform all quality assurance activities in accordance with cGMP and standard operating procedure. | 2/7/2019 |
| 16097 | Halozyme San Diego, CA Research Associate 1, Analytical Testing Support - Contract BS/BA in related field Exp: 1+ years lab experience |
The Research Associate will be a member of the Product Development team at Halozyme and will be responsible for performing analytical testing support, method development, and qualification for in process, drug substance and drug product samples from a variety of drug development programs. Analysis will cover a wide array of analytical techniques such as UV/Vis, ELISA, potency, HPLC, CE, icIEF and wet-chemistry. This individual will also be involved with data verification of laboratory notebooks, protocols, reports, and regulatory filings to ensure the accuracy of the record and to meet critical timelines. | 2/7/2019 |
| 16098 | Auris Health Redwood City, CA Mechanical Engineer BSME or similar Exp: 0-3 years |
Auris is looking for a Mechanical Engineer who will support the design and development of robotic systems for medical applications. This Mechanical Engineer will work closely with engineers from other teams to design and develop robotic equipment that meets clinical, user, and safety requirements. Responsibilities include: design/create electromechanical prototypes, provides hands-on troubleshooting, process and manufacturing support as well as designing implementing, integrating and testing hardware solutions, create design solutions, utilizing engineering methods, etc. | 2/7/2019 |
| 16099 | Harpoon Therapuetics South San Francisco, CA Research Assistant/Associate, Protein Science – Formulation and Analytics BS/BA in biology, biochemistry, or life sciences Exp: 1-2 years |
Harpoon Therapeutics is a startup clinical stage biotechnology company located in South San Francisco, CA. We are focused on the development of novel immune cell engaging therapeutics for oncology indications. We are looking for a motivated, flexible, highly-productive individual who seeks to work in a cross-functional collaborative research environment. As an integral member of the Protein Science group, this individual will partner with the New Technologies, Biology Research, and Translational Medicine groups to develop our proprietary platforms. This position is lab based with the successful candidate primarily engaged in protein formulation and analytics. | 2/7/2019 |
| 16100 | Medtronic Mounds View, MN Component Engineer MS in engineering or science Exp: 0-2 years |
In this exciting role as a Component Engineer you will have responsibility for driving component qualification through effective partnership with external suppliers and internal design and development teams to assure that our products exceed the requirements and expectations of patients, physicians, regulatory agencies and the business. | 2/7/2019 |
| 16101 | FibroGen San Francisco, CA Regulatory Affiars Associate (Temporary) BA/BS in biological science Exp: 0-1 years |
As regulatory representative for assigned clinical studies, provides representation for study-level regulatory activities and updates in study team management meetings, supports clinical trial application activities, reviews and approves investigator document packages including FDA and ex-US submissions, and manages other regulatory aspects of study as directed. | 2/5/2019 |
| 16102 | FibroGen San Francisco, CA Research Associate (Temporary) BA/BS in biological science Exp: 1+ years |
Duties include preparation of biological samples (plasma, urine, etc. and tissue hydrolysates), quantiative analysis of small moleculars by HPLC-MS/MS. | 2/5/2019 |
| 16103 | IDEX Corporation Rochester, NY Mechanical Engineer BS in Mechanical Engineering Exp: 1-3 years |
As a mechanical engineer, individual duties include: develope/execute new product plan in accordance with Pulsafeeder processes, works with marketing to generate product specifications, designs reliable and cost-effective products, etc. | 2/5/2019 |
| 16104 | Fluidda West Hollywood, CA Research Engineer MS in engineering or industral sciences Exp: 0 years |
he research engineer produces specifications for, designs, develops, tests and optimizes the FRI technology. A person in this function performs research on new methodologies needed to address investigative questions. The research engineer combines these with medical science insights and data analysis strategies to come up with an optimal solution for every problem. | 2/5/2019 |
| 16105 | Fluke Everette, WA Mechanical Engineer BS in mechanical engineering Exp: 0-2 years |
As a member of the IG Engineering NPI team, the candidate will be responsible for contributing to the development of mechanical components used in the manufacture of handheld/bench top product enclosures. This includes component and overall system designs that meet Design For Manufacturability (DFM) , compliance to industry standards and Fluke defined product robustness requirements. The role requires a person who is able to interact with a diverse and very skilled team of engineers, collaborate on work tasks across sites and functions, and manage high ambiguity | 2/5/2019 |
| 16106 | Fog Pharma Cambridge, MA RA/SRA, Chemistry BS or MS in chemistry or related Exp: 0-3 years |
We are seeking a highly motivated Research Associate or Senior Research Associate with Peptide Chemistry experience to join our peptide medicinal chemistry team. The individual should have experience in peptide synthesis and purification, peptide libraries, and the optimization of drug like properties with leading molecules. Primary job responsibilities include: Synthesis, purification and analytical characterization of peptides, small proteins and chemically-modified analogs using state-of-the-art synthesis and purification techniques. Program and operate instrumentation such as automated parallel peptide synthesizers, semi-preparative and preparative HPLCs, and an analytical LC/MS | 2/5/2019 |
| 16107 | Pall Life Sciences Cortland, NY R&D Leadership Program BS/BA or MS in engineering or science Exp: 0-2 years |
You will receive both on-the-job training and also specialized learning on key Danaher Business Systems tools like the Problem Solving Process, Kaizen and Visual Project Management. These, plus personal mentoring by senior managers and engineers, will enable you to develop the skills required for key positions within the future organisation. Upon graduation from the program, you will progress to the next stage in your Journey with Pall by moving into a “permanent” role and entering our funnel for future talent. | 2/5/2019 |
| 16108 | Foundation Medicine Cambridge, MA Pathology Research Assistant BS/BA in biology or biochemistry Exp: 0-2 years |
This is a great opportunity for a dedicated, recent graduate looking to gain more experience in molecular genetics as well as the broader functionality of a genomics laboratory committed to advancing the field of precision medicine. As you prepare for the next steps in your career, you will work directly with the pathology team and will assume the following duties: Participate in research projects, led by either the pathologist or yourself, focusing on various aspects of cancer genomics and immunohistochemistry through data gathering, data analysis, figure creation and writing manuscripts. Participate in projects, led by either the pathologist or yourself, focusing on quality improvement/quality assurance of laboratory operations and workflow through team collaboration with data gathering, data analysis, generation of metrics, internal presentations and/or manuscript synthesis and submission. | 2/5/2019 |
| 16109 | Micro Medicine Waltham, MA Research Associate BA/BS in biological science or related Exp: 1-3 years research experience |
This opportunity, you will report to the Director of R&D and work with the Research and Product Development teams to both support existing applications and assist in the development of new applications in diagnostic, therapeutic, and research markets. Duties include processing clinical samples, including blood and blood products, employing safe, accurate, and repeatable methods, gathering data and information to identify best methods, materials, and technologies for cell and molecular assays, etc. | 2/5/2019 |
| 16110 | Frontage Exton, PA Associate Scientist-Product Development- CMC MS in Pharm. Sciences, polymer chem, microbiology, or chemical engineering Exp: 0-4 years |
Responsibilities as an associate scientist-product development include: Perform assigned tasks per procedures compliant with cGMPs and participate in the clinical manufacturing of parenteral, ophthalmic, and other sterile dosage forms, Assist with manufacturing area maintenance such as area monitoring and qualification, purchase of gowning supplies, purchase of equipment and room cleaning supplies, microbiological monitoring supplies, Execute product development studies under the guidance of supervisor or lead project scientist to support formulation development (R&D), and clinical drug product manufacturing | 2/5/2019 |
| 16111 | FujiFilm College Station, TX Associate Scientist – Downstream Process Development MS in chemistry, biology, or related Exp: 1+ years |
Essential functions as an associate scientist include: Assist in the development, optimization, and scale-up of chromatography processes (including affinity, IEX, HIC, etc.) and filtration processes (including UF/DF, depth filtration, and sterile filtration, etc.), Operation of chromatographic systems (GE AKTA, and other Unicorn based equipment), and Maintaining detailed laboratory notebooks following FDBT procedures. | 2/5/2019 |
| 16112 | FujiFilm Morrisville, NC Scientist I, Downstream Process Development MS Exp: 1+ years |
The successful candidate assists in the planning of, conducting, evaluating, and interpreting routine laboratory experiments. The individual monitors on going experiments and identifies and resolves or suggests alternates or solutions to complex occurrences. The individual understands and applies use of equipment, technology and materials associated with area of expertise and related studies and projects. The individual takes a more active role in non-routine analytical or process development activities. | 2/5/2019 |
| 16113 | FujiFilm College Station, TX Quality Control Chemist I BS/BA in chemistry, biochemistry, or related Exp: 0-1 years |
The Quality Control Chemist I, under general direction, will be responsible for performing routine and non-routine quantitative and qualitative analysis of samples submitted to the Quality Control (QC) Laboratory. Essential functions include: Assist in quality control testing of samples provided to the QC laboratory (SDS Page, western blot, ph/conductivity), Assist with preparing and executing test qualification and validation of QC test methods, and Assist with writing Standard Operating Procedures (SOPs) and other related Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP) documentation. | 2/5/2019 |
| 16114 | FujiFilm Durham, NC Manufacturing Process Engineer I BS/BA in science, engineering or related Exp: 1-3 years |
The ideal candidate works independently and with colleagues to provide assistance for the design, development, standardization and maintenance of an operational biotechnology utilized in the manufacture of proteins and drug substances. This person would become familiar with a variety of core manufacturing and operational technologies including equipment used in: Fermentation, Cell Culture/Single Use Technology, Filtration, Centrifugation and Chromatography, Mixing and Buffer Preparation, Parts washing and Sterilization, and Homogenization | 2/5/2019 |
| 16115 | FujiFilm College Station, TX Associate Scientist - Upstream Process Development MS in chemistry, biology, or related Exp: 1+ years |
The Associate Scientist - Upstream Process Development will assist in the development and execution of experiments for the development, optimization, and characterization of cell-based and viral vaccine processes and will be involved in experimental design, data analysis, and interpretation. This individual will assist the Process and Analytical Development Teams to drive processes towards robust Phase I and Phase II GMP manufacturing processes for multiple viral projects and provide technical support for associated regulatory filings. The individual should have familiarity with a range of cell-based and viral vaccine production technologies, including cell and virus expansion, infection, scale-up, harvest and filtration technologies.The successful candidat will also be experienced in basic laboratory analytical techniques (SDS-PAGE, Western blots, spectroscopy, pH/conductivity meters, etc.) | 2/5/2019 |
| 16116 | Fulcrum Therapeutics Cambridge, MA Bioinformatics Engineer BA/BS in engineering or life sciences Exp: 1+ years |
Fulcrum is seeking a Bioinformatics Engineer to (1) implement and manage lab informatics software applications utilized across research teams and (2) build and sustain custom software in the Computational Biology group. Lab informatics includes applications such as GeneData, Dotmatics, LIMS-biorepository systems, cheminformatics tools, and relational databases. Working closely with the IT/Operations and Molecular Sciences groups at Fulcrum, this individual will manage these applications on the cloud in a secure manner, serve as the point of contact with application vendors, organize training, and operate on an efficient budget. Custom software development within Computational Biology will be focused on, but not limited to, molecular profiling pipelines. | 2/5/2019 |
| 16117 | Gene Dx Gaithersburg, MD DNA Sequencing Lab Technician BS/BA in biology or biochemistry Exp: 0-2 years |
This position is for an entry level DNA technician position in our laboratory. The job involves following basic protocols for PCR, gel electrophoresis, and Sanger sequencing. The Technician will be trained to use the various robots and instruments used to automate our PCR and sequencing workflows. At times technicians will be working as part of a team but would also be responsible for a good amount of individual work. Our work is clinical in nature and is repetitive, so this position absolutely requires someone who is very focused, meticulous, and willing to see that there are small things to learn every day. Implement the standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping | 2/5/2019 |
| 16118 | Gene Dx Elmwood Park, NJ Marketing Product Associate BS/BA in science or MS in biological sciences Exp: 0-2 years |
The GeneDx Marketing Product Associate plans and coordinates product test development, launch, and marketing functions. Primary duties include: Helps identify and analyze, in conjunction with marketing and test development groups, promising areas of research or technology that address unmet needs and have large potential markets, Builds processes for transitioning products form test development to marketing, and Works closely with the clinical and design teams on materials such as scientific posters, presentations and publications | 2/5/2019 |
| 16119 | Gene Dx Gaithersburg, MD Cytogenetics Lab Technician BS/BA in biology, biochemistry, or life sciences Exp: 0-2 years |
The Laboratory Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease, using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. Responsibilities include: Implements standard operating procedures for specimen handling and processing, Assess and process prenatal specimens for DNA extraction and sendout testing | 2/5/2019 |
| 16120 | Genewiz Research Triangle Park, NC Laboratory Technician I, Genetic Analysis HS Diploma, or AAS Exp: 1+ years |
Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. Customer focused. Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. | 2/5/2019 |
| 16121 | Genewiz San Diego, CA Sales Associate I BS/BA degree in biology or life sciences Exp: 1 year |
Responsibilities as a sales associate include: Achieve annual sales goals within defined territory/accounts through the development, maintenance, and enhancement of customer accounts, Retain current business baseline revenue by managing relationships with customers and other account contacts by collaborating with business leaders and the customer interface teams and, Drive the marketing process for the territory by creating a marketing plan, registering/planning/ attending local vendor shows, and working with Marketing to follow up on leads from email campaigns | 2/5/2019 |
| 16122 | Genewiz South Plainfield, NJ Sample Management Coordinator, Logistics HS Diploma or BS/BA in biological sciences Exp: 0-1 years |
A Sample Management Coordinator is: A multi-tasker while keeping in mind the details. They help us to carry-out shipment, receipt, tracking and handling of samples. They partner with the sample management team to troubleshoot and resolve sample related issues. They communicate with internal and external customers via email and/or phone and manage project tracking logs. They use online tools for sample submission and data uploading. They manage internal/external storage and shipping of samples. They address, record and track communication related to project samples. They work to manage tasks related to sample management for numerous customer accounts. They help to provide administrative, internal and external support for distribution. | 2/5/2019 |
| 16123 | GenMark Diagnostics Carlsbad, CA Research Associate II MS in biological sciences Exp: 1+ years |
Essential Duties and Responsibilities: Responsible for day to day running of experiments and data analysis, conducts general molecular biology tasks, including nucleic acid purification, quantification, amplification and analysis on multiple platforms, prepares reagents and solutions as needed, using appropriate procedural and documentation methods, maintains stockroom supplies and inventory, prepares documents meeting company standards, including data summaries, reports, SOPs and procedures, presents work at meetings as required, and proposes new strategies and methods to address immediate and upcoming technical issues | 2/5/2019 |
| 16124 | EuroFins Rahway, NJ Entry Level HPLC/UPLC Scientist BS or MS in chemistry, biochemistry, or related Exp: 0-2 years |
HPLC / UPLC Scientist responsibilities include, but are not limited to, the following: Conducts analysis and experimentation on formulated pharmaceutical materials in the laboratory with minimal supervision and using prescribed procedures, conducting independent chemical analyses of candidate formulations and working closely with formulators to streamline drug product development, evaluating “Fit For Purpose” analytical methods and working closely with the analytical method development team to streamline analytical method development, general knowledge of separations science and hands-on experience in chromatographic analysis, data interpretation and processing | 2/5/2019 |
| 16125 | EuroFins Kalamazoo, MI Biological Development Scientist BS/bA in biology, microbiology, or related biological sciences Exp: 1-2 years |
As a biological developmental scientist, individual responsibilities will include: Quantitate antigens using antibody-based assays including ELISA and Western blot, Generate recombinant DNA constructs using techniques including nucleic acid extraction, PCR, gel electrophoresis, plasmid DNA cloning, and bacterial transformation, Maintain cell cultures and perform transfection for transient protein expression | 2/5/2019 |
| 16126 | Genomatica San Diego, CA Fermentation Associate I/II BS/BA in life sciences Exp: 1-3 years |
Genomatica is seeking a highly motivated Research Associate, Molecular Biology to join the Strain Engineering team. This team is responsible for construction, characterization, evolution and fermentation of host strains. The successful candidate will utilize her/his knowledge of molecular biology for cloning of relevant genes into various single-gene and multi-gene DNA constructs using a high-throughput, automated platform. | 2/5/2019 |
| 16127 | Genome DX Biosciences San Diego, CA Sample Processor I BS/BA Exp: 1+ years lab experience |
The Sample Processer’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the GenomeDx internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. | 2/5/2019 |
| 16128 | Neo Genomics Aliso Viejo, CA Associate Project Manager AS or equivalent Exp: 1+ years |
The Pharma Services Associate Project Manager performs tasks for multiple projects as part of project teams. Projects are usually sponsored by pharmaceutical, medical device, or diagnostic testing companies. This role works on projects involving biology, bioinformatics, engineering, software, and other technical disciplines. You will work under the supervision of the responsible Project Manager, Senior Project Manager, or Director. | 2/5/2019 |
| 16129 | Neo Genomics Aliso Viejo, CA Clinical Laboratory Technologist I or II BS in cytogenetics or biological sciences Exp: 1+ years |
In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. | 2/5/2019 |